Method for producing high-purity fluoropolymer-containing composition, and high-purity fluoropolymer-containing composition

Abstract

To provide a method for producing a high purity fluoropolymer-containing composition.SOLUTION: Provided is a method for producing a high purity fluoropolymer-containing composition, the method comprising performing a fluorine radical treatment on a composition containing a fluoropolymer and a polymer (I) containing a polymerization unit (I) derived from a monomer (I) represented by general formula (I) to obtain a high purity fluoropolymer-containing composition: CX1X3=CX2R(-CZ1Z2-A0)m (I) wherein X1 and X3 are each independently F, Cl, H, or CF3; X2 is H, F, an alkyl group, or a fluorine-containing alkyl group; A0 is an anionic group; R is a linking group; Z1 and Z2 are each independently H, F, an alkyl group, or a fluorine-containing alkyl group; and m is an integer of 1 or more.SELECTED DRAWING: None

Description

[Technical Field]

[0001] FIELD OF THE DISCLOSURE The present disclosure relates to a method for producing a high-purity fluoropolymer-containing composition and to a high-purity fluoropolymer-containing composition. [Background technology]

[0002] Patent Document 1 describes particles containing a bulk of a fluoropolymer and a core of a fluorinated ionomer.

[0003] Patent Document 2 describes a method for producing a fluoropolymer, which includes a step of obtaining a fluoropolymer by polymerizing a fluoromonomer in an aqueous medium in the presence of a polymer (1) containing polymerized units (1) based on a monomer represented by the following general formula (1): CX2=CY(-CZ2-O-Rf-A) (1) (In the formula, X's are the same or different and are -H or -F; Y's are -H, -F, an alkyl group or a fluorine-containing alkyl group; Z's are the same or different and are -H, -F, an alkyl group or a fluoroalkyl group; Rf's are fluorine-containing alkylene groups having 1 to 40 carbon atoms or fluorine-containing alkylene groups having 2 to 100 carbon atoms and an ether bond; A's are -COOM, -SO3M or -OSO3M (M's are -H, a metal atom, -NR 7 4. An optionally substituted imidazolium, an optionally substituted pyridinium, or an optionally substituted phosphonium, wherein R 7 is H or an organic group, provided that at least one of X, Y, and Z contains a fluorine atom.

[0004] Patent Document 3 describes a method for producing an aqueous fluoropolymer dispersion, which comprises a step A of carrying out ultrafiltration, microfiltration, or dialysis membrane treatment, or a combination thereof, on a pre-treatment aqueous dispersion containing a fluoropolymer (excluding the polymer (I)) obtained by polymerization in the presence of a polymer (I) containing polymerization units (I) based on a monomer represented by the following general formula (I): CX 1 X 3 =CX2 R(-CZ 1 Z 2 -A 0 ) m (I) (In the formula, X 1 and X 3 are each independently F, Cl, H, or CF; X 2 is H, F, an alkyl group or a fluorine-containing alkyl group; A 0 is an anionic group; R is a linking group; Z 1 and Z 2 are each independently H, F, an alkyl group or a fluorine-containing alkyl group; and m is an integer of 1 or more. [Prior art documents] [Patent documents]

[0005] [Patent Document 1] International Publication No. 2010 / 075494 [Patent Document 2] International Publication No. 2019 / 168183 [Patent Document 3] International Publication No. 2020 / 218620 Summary of the Invention [Problem to be solved by the invention]

[0006] The present disclosure aims to provide a method for producing a high purity fluoropolymer-containing composition. [Means for solving the problem]

[0007] According to the present disclosure, there is provided a method for producing a high-purity fluoropolymer-containing composition, in which a composition containing a fluoropolymer and a polymer (I) including polymerized units (I) based on a monomer (I) represented by general formula (I) is subjected to fluorine radical treatment to obtain a high-purity fluoropolymer-containing composition. CX 1 X 3 =CX 2 R(-CZ 1 Z2 -A 0 ) m (I) (In the formula, X 1 and X 3 are each independently F, Cl, H, or CF; X 2 is H, F, an alkyl group or a fluorine-containing alkyl group; A 0 is an anionic group; R is a linking group; Z 1 and Z 2 are each independently H, F, an alkyl group or a fluorine-containing alkyl group; and m is an integer of 1 or greater.

[0008] In the manufacturing method of the present disclosure, A in general formula (I) 0 -SO3M, -COOM or -P(O)(OM)2 (wherein M is H, a metal atom, NR 7 4. An optionally substituted imidazolium, an optionally substituted pyridinium, or an optionally substituted phosphonium, wherein R 7 is H or an organic group. In the manufacturing method of the present disclosure, A in general formula (I) 0 -COOM (wherein M is H, a metal atom, NR 7 4. An optionally substituted imidazolium, an optionally substituted pyridinium, or an optionally substituted phosphonium, wherein R 7 is H or an organic group. In the production method of the present disclosure, the ion exchange capacity of the polymer (I) is preferably 1.75 meq / g or more. In the production method of the present disclosure, the ion exchange capacity of the polymer (I) is preferably 2.60 meq / g or more. In the production method of the present disclosure, it is preferable that m is 1 in general formula (I). In the manufacturing method of the present disclosure, the fluoropolymer is preferably polytetrafluoroethylene. In the production method of the present disclosure, it is preferable to obtain a composition containing the fluoropolymer and polymer (I) by polymerizing a fluoromonomer in the presence of polymer (I). In the manufacturing method of the present disclosure, preferably, in the presence of polymer (I), fluoromonomer is polymerized in aqueous medium to obtain an aqueous dispersion that contains the fluoropolymer, polymer (I) and aqueous medium, and then, by coagulating the aqueous dispersion, obtain a composition that contains the fluoropolymer and polymer (I). In the production method of the present disclosure, it is preferable to polymerize the fluoromonomer substantially in the absence of a fluorine-containing surfactant. In the production method of the present disclosure, the fluoromonomer is preferably tetrafluoroethylene or a modified monomer copolymerizable with tetrafluoroethylene. In the production method of the present disclosure, the fluoromonomer is preferably tetrafluoroethylene and at least one selected from the group consisting of hexafluoropropylene, perfluoro(alkyl vinyl ether), and perfluoroallyl ether.

[0009] The present disclosure also provides a high-purity fluoropolymer-containing composition obtained by the above-described production method. [Effects of the Invention]

[0010] According to the present disclosure, a method for producing a high purity fluoropolymer-containing composition can be provided. DETAILED DESCRIPTION OF THE INVENTION

[0011] Before specifically describing the present disclosure, some terms used in the present disclosure will be defined or explained.

[0012] In the present disclosure, fluororesins are partially crystalline fluoropolymers, or fluoroplastics. Fluororesins have a melting point and are thermoplastic, but may be melt-processable or non-melt-processable.

[0013] In the present disclosure, melt-processable means that the polymer can be melted and processed using conventional processing equipment such as an extruder, an injection molding machine, etc. Therefore, melt-processable fluororesins usually have a melt flow rate of 0.01 to 500 g / 10 min, as measured by the measurement method described below.

[0014] In the present disclosure, polytetrafluoroethylene [PTFE] is preferably a fluoropolymer having a tetrafluoroethylene content of 99 mol % or more relative to all polymerized units.

[0015] In the present disclosure, any fluororesin (excluding polytetrafluoroethylene) is preferably a fluoropolymer having a tetrafluoroethylene content of less than 99 mol% relative to all polymerized units.

[0016] In the present disclosure, the content of each monomer constituting the fluoropolymer can be calculated by appropriately combining NMR, FT-IR, elemental analysis, and X-ray fluorescence analysis depending on the type of monomer.

[0017] In this disclosure, "organic group" means a group containing one or more carbon atoms or a group formed by removing one hydrogen atom from an organic compound. Examples of the "organic group" are: an alkyl group optionally having one or more substituents; an alkenyl group optionally having one or more substituents; an alkynyl group optionally having one or more substituents; a cycloalkyl group optionally having one or more substituents; a cycloalkenyl group optionally having one or more substituents, a cycloalkadienyl group optionally having one or more substituents, an aryl group optionally having one or more substituents; an aralkyl group optionally having one or more substituents; a non-aromatic heterocyclic group optionally having one or more substituents, a heteroaryl group optionally having one or more substituents; cyano group, formyl group, RaO-, RaCO-, RaSO2-, RaCOO-, RaNRaCO-, RaCONRa-, RaOCO-, RaOSO2-, and RaNRbSO2- (In these formulas, Ra independently represents: an alkyl group optionally having one or more substituents; an alkenyl group optionally having one or more substituents; an alkynyl group optionally having one or more substituents; a cycloalkyl group optionally having one or more substituents; a cycloalkenyl group optionally having one or more substituents, a cycloalkadienyl group optionally having one or more substituents, an aryl group optionally having one or more substituents; an aralkyl group optionally having one or more substituents; a non-aromatic heterocyclic group optionally having one or more substituents, or a heteroaryl group optionally having one or more substituents; Rb is independently H or an alkyl group which may have one or more substituents. Includes. The organic group is preferably an alkyl group which may have one or more substituents.

[0018] In the present disclosure, the term "substituent" refers to a substitutable group. Examples of the "substituent" include an aliphatic group, an aromatic group, a heterocyclic group, an acyl group, an acyloxy group, an acylamino group, an aliphatic oxy group, an aromatic oxy group, a heterocyclic oxy group, an aliphatic oxycarbonyl group, an aromatic oxycarbonyl group, a heterocyclic oxycarbonyl group, a carbamoyl group, an aliphatic sulfonyl group, an aromatic sulfonyl group, a heterocyclic sulfonyl group, an aliphatic sulfonyloxy group, an aromatic sulfonyloxy group, a heterocyclic sulfonyloxy group, a sulfamoyl group, an aliphatic sulfonamido group, an aromatic sulfonamido group, a heterocyclic sulfonamido group, an amino group, and an aliphatic amino group. groups, aromatic amino groups, heterocyclic amino groups, aliphatic oxycarbonylamino groups, aromatic oxycarbonylamino groups, heterocyclic oxycarbonylamino groups, aliphatic sulfinyl groups, aromatic sulfinyl groups, aliphatic thio groups, aromatic thio groups, hydroxy groups, cyano groups, sulfo groups, carboxy groups, aliphatic oxyamino groups, aromatic oxyamino groups, carbamoylamino groups, sulfamoylamino groups, halogen atoms, sulfamoylcarbamoyl groups, carbamoylsulfamoyl groups, dialiphatic oxyphosphinyl groups, and diaromatic oxyphosphinyl groups.

[0019] The aliphatic group may be saturated or unsaturated, and may have a hydroxy group, an aliphatic oxy group, a carbamoyl group, an aliphatic oxycarbonyl group, an aliphatic thio group, an amino group, an aliphatic amino group, an acylamino group, a carbamoylamino group, etc. Examples of the aliphatic group include alkyl groups having a total of 1 to 8, preferably 1 to 4, carbon atoms, such as a methyl group, an ethyl group, a vinyl group, a cyclohexyl group, and a carbamoylmethyl group.

[0020] The aromatic group may have, for example, a nitro group, a halogen atom, an aliphatic oxy group, a carbamoyl group, an aliphatic oxycarbonyl group, an aliphatic thio group, an amino group, an aliphatic amino group, an acylamino group, a carbamoylamino group, etc. Examples of the aromatic group include aryl groups having 6 to 12 carbon atoms, preferably 6 to 10 carbon atoms in total, such as a phenyl group, a 4-nitrophenyl group, a 4-acetylaminophenyl group, and a 4-methanesulfonylphenyl group.

[0021] The heterocyclic group may have a halogen atom, a hydroxy group, an aliphatic oxy group, a carbamoyl group, an aliphatic oxycarbonyl group, an aliphatic thio group, an amino group, an aliphatic amino group, an acylamino group, a carbamoylamino group, etc. Examples of the heterocyclic group include 5- or 6-membered heterocycles having a total of 2 to 12, preferably 2 to 10, carbon atoms, such as a 2-tetrahydrofuryl group and a 2-pyrimidyl group.

[0022] The acyl group may have an aliphatic carbonyl group, an arylcarbonyl group, a heterocyclic carbonyl group, a hydroxy group, a halogen atom, an aromatic group, an aliphatic oxy group, a carbamoyl group, an aliphatic oxycarbonyl group, an aliphatic thio group, an amino group, an aliphatic amino group, an acylamino group, a carbamoylamino group, etc. Examples of the acyl group include acyl groups having a total of 2 to 8, preferably 2 to 4, carbon atoms, such as an acetyl group, a propanoyl group, a benzoyl group, and a 3-pyridinecarbonyl group.

[0023] The acylamino group may have an aliphatic group, an aromatic group, a heterocyclic group, etc., such as an acetylamino group, a benzoylamino group, a 2-pyridinecarbonylamino group, a propanoylamino group, etc. Examples of the acylamino group include acylamino groups having a total of 2 to 12 carbon atoms, preferably 2 to 8 carbon atoms, and alkylcarbonylamino groups having a total of 2 to 8 carbon atoms, such as an acetylamino group, a benzoylamino group, a 2-pyridinecarbonylamino group, a propanoylamino group, etc.

[0024] The aliphatic oxycarbonyl group may be saturated or unsaturated, and may have a hydroxy group, an aliphatic oxy group, a carbamoyl group, an aliphatic oxycarbonyl group, an aliphatic thio group, an amino group, an aliphatic amino group, an acylamino group, a carbamoylamino group, etc. Examples of the aliphatic oxycarbonyl group include alkoxycarbonyl groups having a total of 2 to 8, preferably 2 to 4, carbon atoms, such as a methoxycarbonyl group, an ethoxycarbonyl group, and a (t)-butoxycarbonyl group.

[0025] The carbamoyl group may have an aliphatic group, an aromatic group, a heterocyclic group, etc. Examples of the carbamoyl group include an unsubstituted carbamoyl group, an alkylcarbamoyl group having a total of 2 to 9 carbon atoms, preferably an unsubstituted carbamoyl group, or an alkylcarbamoyl group having a total of 2 to 5 carbon atoms, such as an N-methylcarbamoyl group, an N,N-dimethylcarbamoyl group, or an N-phenylcarbamoyl group.

[0026] The aliphatic sulfonyl group may be saturated or unsaturated and may have a hydroxy group, an aromatic group, an aliphatic oxy group, a carbamoyl group, an aliphatic oxycarbonyl group, an aliphatic thio group, an amino group, an aliphatic amino group, an acylamino group, a carbamoylamino group, etc. Examples of the aliphatic sulfonyl group include alkylsulfonyl groups having a total of 1 to 6 carbon atoms, preferably 1 to 4 carbon atoms, such as a methanesulfonyl group.

[0027] The aromatic sulfonyl group may have a hydroxy group, an aliphatic group, an aliphatic oxy group, a carbamoyl group, an aliphatic oxycarbonyl group, an aliphatic thio group, an amino group, an aliphatic amino group, an acylamino group, a carbamoylamino group, etc. Examples of the aromatic sulfonyl group include arylsulfonyl groups having a total of 6 to 10 carbon atoms, such as a benzenesulfonyl group.

[0028] The amino group may have an aliphatic group, an aromatic group, a heterocyclic group, or the like.

[0029] The acylamino group may have, for example, an acetylamino group, a benzoylamino group, a 2-pyridinecarbonylamino group, a propanoylamino group, etc. Examples of the acylamino group include an acylamino group having a total of 2 to 12 carbon atoms, preferably a total of 2 to 8 carbon atoms, and more preferably an alkylcarbonylamino group having a total of 2 to 8 carbon atoms, such as an acetylamino group, a benzoylamino group, a 2-pyridinecarbonylamino group, a propanoylamino group, etc.

[0030] The aliphatic sulfonamide group, aromatic sulfonamide group, and heterocyclic sulfonamide group may be, for example, a methanesulfonamide group, a benzenesulfonamide group, or a 2-pyridinesulfonamide group.

[0031] The sulfamoyl group may have an aliphatic group, an aromatic group, a heterocyclic group, etc. Examples of the sulfamoyl group include a sulfamoyl group, an alkylsulfamoyl group having 1 to 9 carbon atoms in total, a dialkylsulfamoyl group having 2 to 10 carbon atoms in total, an arylsulfamoyl group having 7 to 13 carbon atoms in total, and a heterocyclic sulfamoyl group having 2 to 12 carbon atoms in total, more preferably a sulfamoyl group, an alkylsulfamoyl group having 1 to 7 carbon atoms in total, a dialkylsulfamoyl group having 3 to 6 carbon atoms in total, an arylsulfamoyl group having 6 to 11 carbon atoms in total, and a heterocyclic sulfamoyl group having 2 to 10 carbon atoms in total, such as a sulfamoyl group, a methylsulfamoyl group, an N,N-dimethylsulfamoyl group, a phenylsulfamoyl group, and a 4-pyridine sulfamoyl group.

[0032] The aliphatic oxy group may be saturated or unsaturated and may have a methoxy group, an ethoxy group, an i-propyloxy group, a cyclohexyloxy group, a methoxyethoxy group, etc. Examples of the aliphatic oxy group include alkoxy groups having a total of 1 to 8 carbon atoms, preferably 1 to 6 carbon atoms, such as a methoxy group, an ethoxy group, an i-propyloxy group, a cyclohexyloxy group, and a methoxyethoxy group.

[0033] The aromatic amino group and heterocyclic amino group may have an aliphatic group, an aliphatic oxy group, a halogen atom, a carbamoyl group, a heterocyclic group fused with the aryl group, an aliphatic oxycarbonyl group, preferably an aliphatic group having 1 to 4 carbon atoms in total, an aliphatic oxy group having 1 to 4 carbon atoms in total, a halogen atom, a carbamoyl group having 1 to 4 carbon atoms in total, a nitro group, or an aliphatic oxycarbonyl group having 2 to 4 carbon atoms in total.

[0034] The aliphatic thio group may be saturated or unsaturated and includes alkylthio groups having a total of 1 to 8 carbon atoms, more preferably 1 to 6 carbon atoms, such as a methylthio group, an ethylthio group, a carbamoylmethylthio group, and a t-butylthio group.

[0035] The carbamoylamino group may have an aliphatic group, an aryl group, a heterocyclic group, etc. Examples of the carbamoylamino group include a carbamoylamino group, an alkylcarbamoylamino group having 2 to 9 carbon atoms in total, a dialkylcarbamoylamino group having 3 to 10 carbon atoms in total, an arylcarbamoylamino group having 7 to 13 carbon atoms in total, and a heterocyclic carbamoylamino group having 3 to 12 carbon atoms in total, preferably a carbamoylamino group, an alkylcarbamoylamino group having 2 to 7 carbon atoms in total, a dialkylcarbamoylamino group having 3 to 6 carbon atoms in total, an arylcarbamoylamino group having 7 to 11 carbon atoms in total, and a heterocyclic carbamoylamino group having 3 to 10 carbon atoms in total, such as a carbamoylamino group, a methylcarbamoylamino group, an N,N-dimethylcarbamoylamino group, a phenylcarbamoylamino group, and a 4-pyridinecarbamoylamino group.

[0036] In this disclosure, ranges expressed by endpoints include all numbers subsumed within that range (e.g., 1 to 10 includes 1.4, 1.9, 2.33, 5.75, 9.98, etc.).

[0037] In this disclosure, the term "at least 1" includes all numbers greater than or equal to 1 (e.g., at least 2, at least 4, at least 6, at least 8, at least 10, at least 25, at least 50, at least 100, etc.).

[0038] Specific embodiments of the present disclosure will be described in detail below, but the present disclosure is not limited to the following embodiments.

[0039] The production method of the present disclosure is a method for producing a high-purity fluoropolymer-containing composition by subjecting a composition containing a fluoropolymer (excluding polymer (I)) and polymer (I) containing polymerization units (I) based on monomer (I) represented by general formula (I) to fluorine radical treatment.

[0040] Patent Documents 2 and 3 describe polymerization of a fluoromonomer in an aqueous medium in the presence of a specific polymer having an anionic group. According to this production method, a composition containing a fluoropolymer and the specific polymer can be obtained as an aqueous dispersion. Furthermore, by coagulating the fluoropolymer in the resulting aqueous dispersion, a powdered composition containing the fluoropolymer and the specific polymer can be obtained. Furthermore, by molding the powdered composition, a composition containing a fluoropolymer and the specific polymer having a desired shape can be obtained. However, if the content of the specific polymer in the composition is too high, the excellent properties of the fluoropolymer may not be fully exhibited. Therefore, there is a need for a production method for a high-purity fluoropolymer-containing composition that can remove as much of the specific polymer as possible and improve the purity of the fluoropolymer in the composition.

[0041] In the production method of the present disclosure, a composition containing a fluoropolymer and polymer (I) is subjected to fluorine radical treatment. By performing the fluorine radical treatment, the polymer (I) in the composition can be removed. As a result, a high-purity fluoropolymer-containing composition can be produced by the production method of the present disclosure.

[0042] The high-purity fluoropolymer-containing composition obtained by the production method of the present disclosure has a high fluoropolymer purity. Therefore, by heating the high-purity fluoropolymer-containing composition and molding it into a desired shape, a molded article with little coloring can be obtained. Furthermore, the amount of gas generated when the high-purity fluoropolymer-containing composition is heated and molded is small, allowing for a molded article with few molding defects such as cracks to be obtained. Furthermore, since a molded article containing a fluoropolymer at high purity can be obtained, the excellent properties of the fluoropolymer obtained will be fully exhibited in the molded article. For example, the excellent insulating properties and electrical properties of the fluoropolymer will be fully exhibited in the molded article obtained.

[0043] The content of polymer (I) in the composition to be subjected to fluorine radical treatment is preferably 0.001% by mass or more, more preferably 0.005% by mass or more, even more preferably 0.01% by mass or more, still more preferably 0.05% by mass or more, particularly preferably 0.10% by mass or more, and most preferably more than 0.20% by mass, based on the fluoropolymer. The content of polymer (I) in the composition is preferably 10% by mass or less, more preferably 5.0% by mass or less, even more preferably 2.0% by mass or less, particularly preferably 1.0% by mass or less, and most preferably 0.50% by mass or less, based on the fluoropolymer.

[0044] The total content of the fluoropolymer and polymer (I) in the composition to be subjected to the fluorine radical treatment is preferably 90% by mass or more, more preferably 99% by mass or more, and even more preferably 99.5% by mass or more, relative to the composition, and may be substantially 100% by mass.

[0045] By carrying out the fluorine radical treatment, 80% by mass or more of the polymer (I) contained in the composition to be subjected to the fluorine radical treatment can be removed from the composition. The removal rate of the polymer (I) is preferably 85% by mass or more, more preferably 90% by mass or more, even more preferably 95% by mass or more, still more preferably 97% by mass or more, particularly preferably 98% by mass or more, and most preferably 99% by mass or more, based on 100% by mass of the content of the polymer (I) contained in the composition to be subjected to the fluorine radical treatment.

[0046] By carrying out the fluorine radical treatment, a high-purity fluoropolymer-containing composition containing polymer (I) of 10 mass ppm or less relative to the fluoropolymer can be obtained. The content of polymer (I) contained in the high-purity fluoropolymer-containing composition is preferably 1 mass ppm or less, more preferably 500 mass ppb or less, even more preferably 100 mass ppb or less, particularly preferably 50 mass ppb or less, and most preferably 25 mass ppb or less relative to the fluoropolymer. The content of polymer (I) contained in the high-purity fluoropolymer-containing composition may be below the detection limit.

[0047] A composition containing a fluoropolymer and polymer (I) is usually obtained by polymerizing a fluoromonomer in an aqueous medium using the polymer (I). Therefore, the impurities in the composition are mainly the polymer (I) and the aqueous medium in the composition. Furthermore, since the polymer (I) has an anionic group, the composition tends to easily absorb moisture. Furthermore, the anionic group itself tends to easily decompose upon heating, etc., to produce volatile substances. Therefore, the purity of the high-purity fluoropolymer-containing composition obtained by the production method of the present disclosure can be confirmed by determining the content of the polymer (I) and volatile components such as moisture and volatile substances in the high-purity fluoropolymer-containing composition. That is, in the present disclosure, it can be confirmed that a high-purity fluoropolymer-containing composition has been obtained when the content of the polymer (I) and volatile components in the composition is lower than the content of those components in the composition to be subjected to fluorine radical treatment.

[0048] The content of polymer (I) in the composition can be determined by solid-state NMR measurement or melt NMR measurement. When polymer (I) contains a carbonyl group, it can also be determined by a Fourier transform infrared spectrometer. Further, WO 2014 / 099453, WO 2010 / 075497, WO 2010 / 075496, WO 2011 / 008381, WO 2009 / 055521, WO 1987 / 007619, JP 61-293476 A, WO 2010 / 075494, WO 2010 / 075359, WO 2012 / 082454, WO 2006 / 119224, WO 2013 / 085864, Methods for measuring the content of each polymer are described in JP-A-2012 / 082707, JP-A-2012 / 082703, JP-A-2012 / 082451, JP-A-2006 / 135825, JP-A-2004 / 067588, JP-A-2009 / 068528, JP-A-2004-075978, JP-A-2001-226436, JP-A-1992 / 017635, JP-A-2014 / 069165, JP-A-11-181009, etc. As a method for measuring the content of polymer (I), the methods for measuring each polymer described therein can be used.

[0049] The form of the high-purity fluoropolymer-containing composition obtained by the production method of the present disclosure is not particularly limited, and may be a powder or a molded product such as a pellet, film, tube, fiber, rod, thread, or tape.

[0050] When the high-purity fluoropolymer-containing composition is a powder, the powder preferably has an average particle size (average secondary particle size) of 100 to 2000 μm. The lower limit of the average secondary particle size is more preferably 200 μm or more, and even more preferably 300 μm or more. The upper limit of the average secondary particle size is preferably 1000 μm or less, more preferably 800 μm or less, and particularly preferably 700 μm or less. The above average secondary particle size is a value measured in accordance with JIS K 6891.

[0051] The total content of the fluoropolymer and polymer (I) in the high-purity fluoropolymer-containing composition is preferably 90% by mass or more, more preferably 99% by mass or more, and even more preferably 99.5% by mass or more, relative to the composition, and may be substantially 100% by mass.

[0052] (Fluorine radical treatment) In the production method of the present disclosure, a composition containing a fluoropolymer and polymer (I) is subjected to a fluorine radical treatment.

[0053] The fluorine radical treatment method may be, for example, a method of exposing a composition containing a fluoropolymer and polymer (I) to a fluorine radical source that generates fluorine radicals. In addition to fluorine gas, the fluorine radical source may also be CoF3, AgF2, UF6, OF2, N2F2, CF3OF, halogen fluorides (e.g., IF, IF3, IF5, IF7, etc.) n (n is 1 to 7; ClF, ClF3, BrF3, etc.), rare gas fluorides (XeF2, XeF4, KrF2, etc.), and nitrogen-containing fluorine compounds (NF3, NF2, etc.). Among these, fluorine gas is most preferred from the viewpoints of ease of handling and cost, ability to remove polymer (I) with high efficiency, and the fact that it is unlikely to give rise to new impurities such as iodine.

[0054] Since the reaction with the fluorine radical source is highly exothermic, the fluorine radical source may be diluted with an inert gas such as nitrogen.

[0055] The level of fluorine radical source in the fluorine radical source / inert gas mixture can be from 1 to 100% by volume, but is preferably from about 5 to about 25% by volume due to the high hazards of working with pure fluorine. For fluoropolymers that exhibit severe thermally induced discoloration, the fluorine radical source / inert gas mixture may be sufficiently diluted to prevent overheating of the fluoropolymer and the attendant fire hazard.

[0056] The temperature of the fluorine radical treatment is preferably above 100°C. The temperature of the fluorine radical treatment is more preferably 110°C or higher, even more preferably 120°C or higher, even more preferably 130°C or higher, and especially preferably 150°C or higher. Furthermore, it is particularly preferably 170°C or higher, even more preferably 180°C or higher, even more preferably 200°C or higher, especially preferably 210°C or higher, especially preferably 220°C or higher, and most preferably 230°C or higher. Furthermore, the temperature of the fluorine radical treatment is preferably 310°C or lower, more preferably 300°C or lower, even more preferably 290°C or lower, even more preferably 280°C or lower, especially preferably 270°C or lower, especially preferably 250°C or lower, and most preferably 240°C or lower. If the temperature is too low, the polymer (I) may not be sufficiently removed. In particular, when the fluoropolymer is polytetrafluoroethylene (PTFE), if the temperature of the fluorine radical treatment is too high, the friction between the PTFE particles can easily cause fibrillation even with a small shear force, leading to the loss of the original particle structure, which may result in a decrease in paste extrusion performance.

[0057] In the fluorine radical treatment, the amount of the fluorine radical source added is preferably 0.5 parts by mass or more relative to 100 parts by mass of the fluoropolymer. More preferably, it is 0.8 parts by mass or more, even more preferably 1.0 parts by mass or more, more preferably 1.6 parts by mass or more, even more preferably 2.0 parts by mass or more, even more preferably 2.5 parts by mass or more, especially preferably 3.0 parts by mass or more, and particularly preferably 5.0 parts by mass or more. Furthermore, the amount of the fluorine radical source added is preferably 35.0 parts by mass or less, more preferably 26.0 parts by mass or less, even more preferably 20.0 parts by mass or less, and particularly preferably 15.0 parts by mass or less. If the amount of the fluorine radical source added is too small, the polymer (I) may not be sufficiently removed. If the amount of the fluorine radical source added is too large, the fluorination effect will not be improved, and this may be uneconomical.

[0058] A suitable combination of the temperature of the fluorine radical treatment and the amount of the fluorine radical source added is a temperature of 100°C or higher and an amount of the fluorine radical source added, calculated as fluorine atoms, of 0.5 parts by mass or more per 100 parts by mass of the fluoropolymer.

[0059] The above combination is preferably 100°C or higher and 1.0 mass parts or higher, more preferably 100°C or higher and 1.6 mass parts or higher, even more preferably 100°C or higher and 2.0 mass parts or higher, even more preferably 100°C or higher and 2.5 mass parts or higher, especially preferably 100°C or higher and 3.0 mass parts or higher, and particularly preferably 100°C or higher and 5.0 mass parts or higher. Furthermore, the above combination is preferably 110°C or higher and 0.5 parts by mass or higher, more preferably 110°C or higher and 1.0 parts by mass or higher, even more preferably 110°C or higher and 1.6 parts by mass or higher, even more preferably 110°C or higher and 2.0 parts by mass or higher, especially preferably 110°C or higher and 2.5 parts by mass or higher, particularly preferably 110°C or higher and 3.0 parts by mass or higher, and most preferably 110°C or higher and 5.0 parts by mass or higher. Furthermore, the above combination is preferably 120°C or higher and 0.5 parts by mass or higher, more preferably 120°C or higher and 1.0 parts by mass or higher, even more preferably 120°C or higher and 1.6 parts by mass or higher, even more preferably 120°C or higher and 2.0 parts by mass or higher, especially preferably 120°C or higher and 2.5 parts by mass or higher, particularly preferably 120°C or higher and 3.0 parts by mass or higher, and most preferably 120°C or higher and 5.0 parts by mass or higher. Furthermore, the above combination is preferably 130°C or higher and 0.5 parts by mass or higher, more preferably 130°C or higher and 1.0 parts by mass or higher, even more preferably 130°C or higher and 1.6 parts by mass or higher, even more preferably 130°C or higher and 2.0 parts by mass or higher, especially preferably 130°C or higher and 2.5 parts by mass or higher, particularly preferably 130°C or higher and 3.0 parts by mass or higher, and most preferably 130°C or higher and 5.0 parts by mass or higher. Furthermore, the above combination is preferably 150°C or higher and 0.5 parts by mass or higher, more preferably 150°C or higher and 1.0 parts by mass or higher, even more preferably 150°C or higher and 1.6 parts by mass or higher, even more preferably 150°C or higher and 2.0 parts by mass or higher, especially preferably 150°C or higher and 2.5 parts by mass or higher, particularly preferably 150°C or higher and 3.0 parts by mass or higher, and most preferably 150°C or higher and 5.0 parts by mass or higher. Furthermore, the above combination is preferably 170°C or higher and 0.5 parts by mass or higher, more preferably 170°C or higher and 1.0 parts by mass or higher, even more preferably 170°C or higher and 1.6 parts by mass or higher, even more preferably 170°C or higher and 2.0 parts by mass or higher, especially preferably 170°C or higher and 2.5 parts by mass or higher, particularly preferably 170°C or higher and 3.0 parts by mass or higher, and most preferably 170°C or higher and 5.0 parts by mass or higher. Furthermore, the above combination is preferably 180°C or higher and 0.5 parts by mass or higher, more preferably 180°C or higher and 1.0 parts by mass or higher, even more preferably 180°C or higher and 1.6 parts by mass or higher, even more preferably 180°C or higher and 2.0 parts by mass or higher, especially preferably 180°C or higher and 2.5 parts by mass or higher, particularly preferably 180°C or higher and 3.0 parts by mass or higher, and most preferably 180°C or higher and 5.0 parts by mass or higher. Furthermore, the above combination is preferably 200°C or higher and 0.5 parts by mass or higher, more preferably 200°C or higher and 1.0 parts by mass or higher, even more preferably 200°C or higher and 1.6 parts by mass or higher, even more preferably 200°C or higher and 2.0 parts by mass or higher, especially preferably 200°C or higher and 2.5 parts by mass or higher, particularly preferably 200°C or higher and 3.0 parts by mass or higher, and most preferably 200°C or higher and 5.0 parts by mass or higher. Furthermore, the above combination is preferably 210°C or higher and 0.5 parts by mass or higher, more preferably 210°C or higher and 1.0 parts by mass or higher, even more preferably 210°C or higher and 1.6 parts by mass or higher, even more preferably 210°C or higher and 2.0 parts by mass or higher, especially preferably 210°C or higher and 2.5 parts by mass or higher, particularly preferably 210°C or higher and 3.0 parts by mass or higher, and most preferably 210°C or higher and 5.0 parts by mass or higher. Furthermore, the above combination is preferably 220°C or higher and 0.5 parts by mass or higher, more preferably 220°C or higher and 1.0 parts by mass or higher, even more preferably 220°C or higher and 1.6 parts by mass or higher, even more preferably 220°C or higher and 2.0 parts by mass or higher, especially preferably 220°C or higher and 2.5 parts by mass or higher, particularly preferably 220°C or higher and 3.0 parts by mass or higher, and most preferably 220°C or higher and 5.0 parts by mass or higher. Furthermore, the above combination is preferably 230°C or higher and 0.5 parts by mass or higher, more preferably 230°C or higher and 1.0 parts by mass or higher, even more preferably 230°C or higher and 1.6 parts by mass or higher, even more preferably 230°C or higher and 2.0 parts by mass or higher, especially preferably 230°C or higher and 2.5 parts by mass or higher, particularly preferably 230°C or higher and 3.0 parts by mass or higher, and most preferably 230°C or higher and 5.0 parts by mass or higher. The temperature of the fluorine radical treatment in the above combination is preferably 310°C or less, more preferably 300°C or less, even more preferably 290°C or less, even more preferably 280°C or less, especially preferably 270°C or less, particularly preferably 250°C or less, and most preferably 240°C or less. The amount of the fluorine radical source added in the above combination is preferably 35.0 parts by mass or less, more preferably 26.0 parts by mass or less, even more preferably 20.0 parts by mass or less, and particularly preferably 15.0 parts by mass or less, per 100 parts by mass of the fluoropolymer. Furthermore, the upper limit combination of the temperature for the fluorine radical treatment and the amount of the fluorine radical source is preferably 240°C or less and 35.0 parts by mass or less, more preferably 240°C or less and 26.0 parts by mass or less, even more preferably 240°C or less and 20.0 parts by mass or less, and particularly preferably 240°C or less and 15.0 parts by mass or less.

[0060] The amount (parts by mass) of the fluorine radical source added per 100 parts by mass of the fluoropolymer is calculated according to the following formula. A = (B / F) × 100 B=C×D×E C = {P / (RT × 1000)} × G × H A: Amount of fluorine radical source added (parts by mass) per 100 parts by mass of fluoropolymer B: Total amount of fluorine radical source added (g) C: Fluorine radical source concentration in the mixed gas (g / mL) D: Mixed gas flow rate (mL / min) E: Fluorine radical treatment time (min) F: Sample (fluoropolymer) filling amount (g) G: Molecular weight of the fluorine radical source (g / mol) H: Ratio of fluorine radical source in the mixed gas In the formula, P, R, and T are as follows: P = pressure (atm) R = 0.082 (atm L / K mol) T=temperature (K)

[0061] Any reactor equipped with a heating device and capable of sufficient solid-gas contact can be used for fluorine radical treatment. Specific examples include fluidized bed and tray-type solid-gas contact reactors.

[0062] From the viewpoint of production stability, the fluorine radical treatment is preferably carried out in a state in which the composition and the fluorine radical source are sealed in a sealable container.

[0063] The pressure for carrying out the fluorine radical treatment is not particularly limited, and the fluorine radical treatment may be carried out under increased pressure or under normal pressure.

[0064] In one embodiment, the fluorine radical treatment can be carried out under normal pressure (e.g., a gauge pressure of 0 to 0.01 MPa). For example, the composition and the fluorine radical source can be sealed in a stainless steel container so that the pressure inside the container is normal pressure. This embodiment is particularly advantageous in terms of stable production.

[0065] From the viewpoint of production efficiency, the fluorine radical treatment is also preferably carried out by a constant flow method (a method in which a fluorine radical source is constantly circulated in a container containing the composition).

[0066] The fluorine radical treatment may be carried out multiple times, for example, two, three, four, five, six, seven, eight, nine, or ten removal steps.

[0067] The production method of the present disclosure may further include a step of heat treating the composition containing the fluoropolymer and polymer (I). The timing of the heat treatment is not particularly limited, and the heat treatment may be performed before or after the fluorine radical treatment, but it is preferable to perform the heat treatment before the fluorine radical treatment.

[0068] The heat treatment method is not particularly limited, and conventionally known methods can be used. When the composition contains PTFE as a fluoropolymer and further contains water in addition to PTFE and polymer (I), it is preferable to perform the heat treatment while keeping the composition in a state where it is not very fluid, preferably while it is left standing, in order to suppress fibrillation of PTFE. The heat treatment may be accompanied by evaporation of water.

[0069] The lower limit of the heat treatment temperature is, in order of preference, 150° C. or higher, 160° C. or higher, 170° C. or higher, 180° C. or higher, 200° C. or higher, 210° C. or higher, 220° C. or higher, and 230° C. The upper limit of the heat treatment temperature is, in order of preference, 310° C. or lower, 300° C. or lower, 290° C. or lower, 280° C. or lower, and 270° C. or lower.

[0070] The production method of the present disclosure may further include a step of washing the composition containing the fluoropolymer and polymer (I) with water or an organic solvent. The timing of washing is not particularly limited, and washing may be performed before or after the fluorine radical treatment, but washing before the fluorine radical treatment is preferred.

[0071] Examples of organic solvents used for washing include ethers, halogenated hydrocarbons, aromatic hydrocarbons, pyridine, nitriles, nitrogen-containing polar organic compounds, dimethyl sulfoxide, and alcohols. Examples of the ether include diethyl ether, tetrahydrofuran, dioxane, and diethylene glycol diethyl ether. Examples of the halogenated hydrocarbon include dichloromethane, dichloroethane, chloroform, chlorobenzene, and o-dichlorobenzene. Examples of the aromatic hydrocarbon include benzene, toluene, and xylene. Examples of the nitrile include acetonitrile, propionitrile, butyronitrile, isobutyronitrile, and benzonitrile. Examples of the nitrogen-containing polar organic compound include N,N-dimethylformamide, N,N-dimethylacetamide, N-methyl-2-pyrrolidone, 2-pyrrolidone, and 1,3-dimethyl-2-imidazolidinone. Examples of the alcohol include methanol, ethanol, 1-propanol, and isopropanol. The above organic solvents may be used in combination.

[0072] The method for washing with water or an organic solvent is not particularly limited, and any conventionally known method can be used.

[0073] The composition to be treated with fluorine radicals, heat-treated, or washed may be in the form of a powder or a molded product such as a pellet, film, tube, fiber, rod, thread, tape, etc. When the composition contains PTFE as the fluoropolymer, the composition containing PTFE and polymer (I) may be stretched, and then the resulting stretched product may be treated with fluorine radicals.

[0074] (Polymer (I)) The polymer (I) used in the production method of the present disclosure is a polymer containing polymerized units (I) based on the monomer (I). The monomer (I) is represented by the following general formula (I). CX 1 X 3 =CX 2 R(-CZ 1 Z 2 -A 0 ) m (I) (In the formula, X 1 and X 3 are each independently F, Cl, H, or CF; X 2 is H, F, an alkyl group or a fluorine-containing alkyl group; A 0 is an anionic group; R is a linking group; Z 1 and Z 2 are each independently H, F, an alkyl group or a fluorine-containing alkyl group; and m is an integer of 1 or greater.

[0075] In the present disclosure, the anionic group includes functional groups that provide anionic groups such as sulfate groups, carboxylate groups, acid groups such as -COOH, acid salt groups such as -COONH4, etc. Examples of anionic groups include sulfate groups, carboxylate groups, phosphate groups, phosphonate groups, sulfonate groups, or -C(CF3)2OM (wherein M is -H, a metal atom, -NR 74. An optionally substituted imidazolium, an optionally substituted pyridinium, or an optionally substituted phosphonium, wherein R 7 is H or an organic group.

[0076] In the production method of the present disclosure, one or more types of monomers can be used as the monomer (I) represented by general formula (I).

[0077] R is a linking group. In the present disclosure, a "linking group" is an (m+1)-valent linking group, and when m is 1, it is a divalent linking group. The linking group may be a single bond and preferably contains at least one carbon atom, and the number of carbon atoms may be 2 or more, 4 or more, 8 or more, 10 or more, or 20 or more. There is no upper limit, but it may be, for example, 100 or less, or 50 or less.

[0078] The linking group may be linear or branched, cyclic or acyclic, saturated or unsaturated, substituted or unsubstituted, and may optionally contain one or more heteroatoms selected from the group consisting of sulfur, oxygen, and nitrogen, and may optionally contain one or more functional groups selected from the group consisting of ester, amide, sulfonamide, carbonyl, carbonate, urethane, urea, and carbamate. The linking group may not contain carbon atoms but may be a catenary heteroatom such as oxygen, sulfur, or nitrogen.

[0079] m is an integer of 1 or more, preferably 1 or 2, and more preferably 1. When m is an integer of 2 or more, Z 1 , Z 2 and A 0 may be the same or different. Next, a preferred structure when m is 1 in general formula (I) will be described.

[0080] R is preferably a catenary heteroatom such as oxygen, sulfur, or nitrogen, or a divalent organic group.

[0081] When R is a divalent organic group, the hydrogen atom bonded to the carbon atom may be replaced with a halogen atom other than fluorine, such as chlorine, and may or may not contain a double bond. R may be either linear or branched, and may be cyclic or acyclic. R may also contain a functional group (e.g., ester, ether, ketone (keto group), amine, halide, etc.).

[0082] R may also be a non-fluorinated divalent organic group, or a partially fluorinated or perfluorinated divalent organic group.

[0083] R may be, for example, a hydrocarbon group in which no fluorine atoms are bonded to the carbon atoms, a hydrocarbon group in which some of the hydrogen atoms bonded to the carbon atoms are substituted with fluorine atoms, or a hydrocarbon group in which all of the hydrogen atoms bonded to the carbon atoms are substituted with fluorine atoms, and these may contain an oxygen atom, a double bond, or a functional group.

[0084] R is preferably a hydrocarbon group having 1 to 100 carbon atoms which may contain an ether bond or a keto group, and in the hydrocarbon group, some or all of the hydrogen atoms bonded to the carbon atoms may be substituted with fluorine.

[0085] R is preferably -(CH2) a -, -(CF2) a -, -(CF2) a -O-, -O-(CF2) a -, -(CF2) a -O-(CF2) b -, -O(CF2) a -O-(CF2) b -, -(CF2) a -[O-(CF2) b ] c -, -O(CF2) a -[O-(CF2) b ] c -, -[(CF2) a -O] b -[(CF2)c -O] d -, -O[(CF2) a -O] b -, -O[(CF2) a -O] b -[(CF2) c -O] d -, -O-[CF2CF(CF3)O] a -(CF2) b -, -O-(CF2) a -O-[CF(CF3)CF2O] b -O-, -O-[CF2CF(CF3)O] a -(CF2) b -O-, -O-[CF2CF(CF3)O] a -(CF2) b -O-[CF(CF3)CF2O] c -O-, -[CF2CF(CF3)O] a -, -[CF(CF3)CF2O] a -, -(CF2) a -O-[CF(CF3)CF2O] a -, -(CF2) a -O-[CF(CF3)CF2O] a -(CF2) b -, -[CF2CF(CF3)] a -CO-(CF2) b - and at least one selected from combinations thereof. In the formula, a, b, c, and d are independently at least 1. a, b, c, and d may independently be 2 or more, 3 or more, 4 or more, 10 or more, or 20 or more. The upper limit of a, b, c, and d is, for example, 100. R is more preferably at least one selected from -O-CF2-, -O-CF2CF2-, -O-CF2CF2-O-, -O-CF2CF2CF2-, -O-CF2CF2CF2-O-, -O-CF2CF(CF3)-O-, -O-CF2CF2-O-CF(CF3)CF2-O-, -O-CF2CF(CF3)-O-CF2CF2-O-, and -O-CF2CF(CF3)-O-CF2-.

[0086] R is represented by the general formula (r1): -CF2-O-(CX 6 2) e -{O-CF(CF3)} f -(O) g - (r1) (In the formula, X 6 are each independently H, F or CF3, e is an integer of 0 to 3, f is an integer of 0 to 3, and g is 0 or 1), and a divalent group represented by the general formula (r2): -CF2-O-(CX 7 2) e -(O) g - (r2) (In the formula, X 7 are each independently H, F or CF3, e is an integer of 0 to 3, and g is 0 or 1), and a divalent group represented by the formula (I) is more preferred.

[0087] Specific examples suitable for R include -CF2-O-, -CF2-O-CF2-, -CF2-O-CH2-, -CF2-O-CH2CF2-, -O-CF2-, -O-CF2CF 2-, -O-CF2CF2CF2-, -O-CF2CF2CF2CF2-, -O-CF2CF(CF3)-O-CF2-, -O-CF2CF(CF3)-O-CF2CF2- , -CF2-O-CF2CF2-, -CF2-O-CF2CH2-, -CF2-O-CF2CF2CH2-, -CF2-O-CF(CF3)-, -CF2-O-CF(CF3 )CF2-, -CF2-O-CF(CF3)CF2-O-, -CF2-O-CF(CF3)CF2-O-CF2-, -CF2-O-CF(CF3)CH2-, and the like. Among these, R is preferably a perfluoroalkylene group which may contain an oxygen atom, specifically, -CF2-O-, -CF2-O-CF2-, -O-CF2-, -O-CF2CF2-, -O-CF2CF(CF3)-O-CF2-, -O-CF2CF(CF3)-O-CF2CF2-, -CF2-O-CF2CF2-, -CF2-O-CF(CF3)-, -CF2-O-CF(CF3)CF2-, or -CF2-O-CF(CF3)CF2-O- is preferred.

[0088] -R-CZ of general formula (I) 1 Z 2 - is a compound represented by the general formula (s1): -CF2-O-(CX 6 2) e -{O-CF(CF3)} f -(O) g -CZ 1 Z 2 - (s1) (In the formula, X 6 are each independently H, F, or CF3, e is an integer of 0 to 3, f is an integer of 0 to 3, g is 0 or 1, and Z 1 and Z 2 are each independently H, F, an alkyl group or a fluorine-containing alkyl group), and in formula (s1), Z 1 and Z 2 More preferably, they are F or CF3, and even more preferably, one is F and the other is CF3.

[0089] In addition, in the general formula (I), -R-CZ 1 Z 2 - as the general formula (s2): -CF2-O-(CX 7 2) e -(O) g -CZ 1 Z 2 - (s2) (In the formula, X 7 are each independently H, F, or CF3, e is an integer of 0 to 3, g is 0 or 1, and Z 1 and Z 2 are each independently H, F, an alkyl group or a fluorine-containing alkyl group), and in formula (s2), Z 1 and Z 2 More preferably, they are F or CF3, and even more preferably, one is F and the other is CF3.

[0090] -R-CZ of general formula (I) 1 Z 2- as -CF2-O-CF2-, -CF2-O-CF(CF3)-, -CF2-OC(CF3)2-, -CF2-O-CF2-CF2-, -CF2-O-CF2-CF(CF3)-, -CF2-O-CF 2-C(CF3)2-, -CF2-O-CF2CF2-CF2-, -CF2-O-CF2CF2-CF(CF3)-, -CF2-O-CF2CF2-C(CF3)2-, -CF2-O-CF(CF3)-CF2 -, -CF2-O-CF(CF3)-CF(CF3)-, -CF2-O-CF(CF3)-C(CF3)2-, -CF2-O-CF(CF3)-CF2-, -CF2-O-CF(CF3)-CF(CF3)-, -CF2-O-CF(CF3)-C(CF3)2-, -CF2-O-CF(CF3)CF2-CF2-, -CF2-O-CF(CF3)CF2-CF(CF3)-, -CF2-O-CF(CF3)CF2-C( CF3)2-, -CF2-O-CF(CF3)CF2-O-CF2-, -CF2-O-CF(CF3)CF2-O-CF(CF3)-, or -CF2-O-CF(CF3)CF2-OC(CF3)2- is preferred. Exactly, -O-CF2CF2-, -O-CF2CF2CF2-, -O-CF2CF2CF2CF2-, -O-CF2CF(CF3)-O-CF2-, -O-CF2CF(CF3)-O-CF2CF2-, -CF 2-O-CF(CF3)-, -CF2-O-CF2-CF(CF3)-, -CF2-O-CF2CF2-CF(CF3)-, -CF2-O-CF(CF3)-CF(CF3)-, -CF2-O-CF(CF3)CF2-CF(CF3)-, or -CF2-O-CF(CF3)CF2-O-CF(CF3)- are more preferred, with -O-CF2CF2- and -O-CF2CF(CF3)-O-CF2CF2- being even more preferred.

[0091] It is also preferred that the polymer (I) is highly fluorinated. For example, it may contain anionic groups (A) such as phosphate moieties (e.g., CH2OP(O)(OM)2) and sulfate moieties (e.g., CH2OS(O)2OM). 0 ), it is preferred that 80% or more, 90% or more, 95% or more, or 100% of the C—H bonds in the polymer (I) are substituted with C—F bonds.

[0092] The monomer (I) and the polymer (I) contain an anionic group (A 0 ) except for the C—F bond, it is also preferable that the compound has no C—H bond. 1 , X 2 , and X 3 are all F, and R is a perfluoroalkylene group having one or more carbon atoms, and the perfluoroalkylene group may be either linear or branched, may be cyclic or acyclic, and may contain at least one catenary heteroatom. The number of carbon atoms in the perfluoroalkylene group may be 2 to 20, or may be 4 to 18.

[0093] The monomer (I) and the polymer (I) may be partially fluorinated. That is, the monomer (I) and the polymer (I) may contain an anionic group (A 0 ), it is also preferred that the alkyl group has at least one hydrogen atom bonded to a carbon atom and at least one fluorine atom bonded to a carbon atom.

[0094] Anionic group (A 0 ) can be —SO2M, —SO3M, —OSO3M, —COOM, —SONR′CH2COOM, —CH2OP(O)(OM)2, [—CH2O]2P(O)(OM), —CH2CH2OP(O)(OM)2, [—CH2CH2O]2P(O)(OM), —CH2CH2OSO3M, —P(O)(OM)2, —SON2NR′CH2CH2OP(O)(OM)2, [—SON2NR′CH2CH2O]2P(O)(OM), —CH2OSO3M, —SON2NR′CH2CH2OSO3M, or —C(CF3)2OM. Of these, -SO3M, -OSO3M, -COOM, -P(O)(OM)2 or -C(CF3)2OM is preferred, -COOM, -SO3M, -OSO3M or -C(CF3)2OM is more preferred, -SO3M, -COOM or -P(O)(OM)2 is even more preferred, -SO3M or -COOM is particularly preferred, and -COOM is most preferred.

[0095] M is H, metal atom, NR7 4. An optionally substituted imidazolium, an optionally substituted pyridinium, or an optionally substituted phosphonium, wherein R 7 is H or an organic group.

[0096] Examples of the metal atom include alkali metals (Group 1) and alkaline earth metals (Group 2), and Na, K or Li is preferred.

[0097] M is -H, a metal atom, or NR 7 4 is preferred, and -H, an alkali metal (Group 1), an alkaline earth metal (Group 2) or NR 7 4 is more preferred, -H, -Na, -K, -Li or NH4 is even more preferred, -H, -Na, -K or NH4 is even more preferred, -H, -Na or NH4 is especially preferred, and -H or -NH4 is most preferred.

[0098] In the polymer (I), each polymer unit (I) may have a different anionic group or may have the same anionic group.

[0099] The monomer (I) is also preferably a monomer represented by the general formula (Ia). The polymer (I) is also preferably a polymer containing polymerized units (Ia) based on a monomer represented by general formula (Ia). CF2=CF-O-Rf 0 -A 0 (Ia) (In the formula, A 0 is an anionic group, and Rf 0 is a perfluorinated divalent linking group that may be linear or branched, cyclic or acyclic in structure, saturated or unsaturated, substituted or unsubstituted, and optionally contains one or more heteroatoms selected from the group consisting of sulfur, oxygen, and nitrogen.

[0100] The monomer (I) is also preferably a monomer represented by the general formula (Ib). The polymer (I) is also preferably a polymer containing polymerized units (Ib) based on a monomer represented by general formula (Ib). CH2=CH-O-Rf 0 -A 0 (Ib) (In the formula, A 0 is an anionic group, and Rf 0 is a perfluorinated divalent linking group defined by formula Ia.

[0101] In general formula (I), A 0 is a sulfate group. 0 is, for example, -CH2OSO3M, -CH2CH2OSO3M, or -SO2NR'CH2CH2OSO3M, where R' is H or an alkyl group having 1 to 4 carbon atoms, and M is the same as above.

[0102] A 0 is a sulfate group, examples of the monomer represented by general formula (I) include CF2=CF(OCF2CF2CH2OSO3M), CF2=CF(O(CF2)4CH2OSO3M), CF2=CF(OCF2CF(CF3)CH2OSO3M), CF2=CF(OCF2CF(CF3)OCF2CF2CH2OSO3M), CH2=CH((CF2)4CH2OSO3M), CF2=CF(OCF2CF2SON(CH3)CH2CH2OSO3M), CH2=CH(CF2CF2CH2OSO3M), CF2=CF(OCF2CF2CF2CF2SON(CH3)CH2CH2OSO3M), CH2=CH(CF2CF2CH2OSO3M), etc. In the above formulas, M is the same as above.

[0103] In general formula (I), A 0 In one preferred embodiment, A is a sulfonate group. 0 An example is -SO3M, where M is the same as above.

[0104] A 0is a sulfonate group, examples of the monomer represented by general formula (I) include CF2=CF(OCF2CF2SO3M), CF2=CF(O(CF2)3SO3M), CF2=CF(O(CF2)4SO3M), CF2=CF(OCF2CF(CF3)SO3M), CF2=CF(OCF2CF(CF3)OCF2CF2SO3M), CH2=CH(CF2CF2SO3M), CF2=CF(OCF2CF(CF3)OCF2CF2CF2CF2SO3M), CH2=CH((CF2)4SO3M), CH2=CH((CF2)3SO3M), etc. In the above formulas, M is the same as above.

[0105] In general formula (I), A 0 A is preferably a carboxylate group. 0 Examples of the compound include COOM or SO2NR'CH2COOM, where R' is H or an alkyl group having 1 to 4 carbon atoms, and M is the same as above. 0 is a carboxylate group, examples of the monomer represented by general formula (I) include CF2=CF(OCF2CF2COOM), CF2=CF(O(CF2)3COOM), CF2=CF(O(CF2)5COOM), CF2=CF(OCF2CF(CF3)COOM), CF2=CF(OCF2CF(CF3)O(CF2) n COOM) (n is greater than 1), CH2=CH(CF2CF2COOM), CH2=CH((CF2)4COOM), CH2=CH((CF2)3COOM), CF2=CF(OCF2CF2SO2NR'CH2COOM), CF2=CF(O(CF2)4SO2NR'CH2COOM), CF2=CF(OCF2CF(CF3)SO2NR'CH2COOM), CF2=CF(OCF2CF(CF3)OCF2CF2SO2NR'CH2COOM), CH2=CH(CF2CF2SO2NR'CH2COOM), CF2=CF(OCF2CF(CF3)OCF2CF2CF2CF2SO2NR'CH2COOM), CH2=CH((CF2)4SO2NR'CH2COOM), CH2=CH((CF2)3SO2NR'CH2COOM). In the above formula, R' is H or an alkyl group having 1 to 4 carbon atoms, and M is the same as above.

[0106] In general formula (I), A 0 In one preferred embodiment, A is a phosphate group. 0 Examples of such a group include -CH2OP(O)(OM)2, [-CHO]2P(O)(OM), -CH2CH2OP(O)(OM)2, [-CH2CH2O]2P(O)(OM), [-SON2NR'CH2CH2O]2P(O)(OM) or SO2NR'CH2CH2OP(O)(OM)2, where R' is an alkyl group having 1 to 4 carbon atoms and M is as defined above.

[0107] A 0 is a phosphate, examples of the monomer represented by general formula (I) include CF2=CF(OCF2CF2CH2OP(O)(OM)2), CF2=CF(O(CF2)4CH2OP(O)(OM)2), CF2=CF(OCF2CF(CF3)CH2OP(O)(OM)2), CF2=CF(OCF2CF(CF3)OCF2CF2CH2OP(O)(OM)2), CF2=CF(O Examples include CF2CF2SO2N(CH3)CH2CH2OP(O)(OM)2), CF2=CF(OCF2CF2CF2CF2SO2N(CH3)CH2CH2OP(O)(OM)2), CH2=CH(CF2CF2CH2OP(O)(OM)2), CH2=CH((CF2)4CH2OP(O)(OM)2), CH2=CH((CF2)3CH2OP(O)(OM)2), etc. In the above formula, M is the same as above.

[0108] In general formula (I), A 0 In one preferred embodiment, A is a phosphonate group. 0is a phosphonate group, examples of the monomer represented by general formula (I) include CF2=CF(OCF2CF2P(O)(OM)2), CF2=CF(O(CF2)4P(O)(OM)2), CF2=CF(OCF2CF(CF3)P(O)(OM)2), CF2=CF(OCF2CF(CF3)OCF2CF2P(O)(OM)2), CH2=CH(CF2CF2P(O)(OM)2), CH2=CH((CF2)4P(O)(OM)2), CH2=CH((CF2)3P(O)(OM)2), where M is the same as above.

[0109] The monomer (I) is preferably a monomer (1) represented by the general formula (1). The polymer (I) is preferably a polymer (1) containing polymerized units (1) based on a monomer represented by general formula (1). CX2=CY(-CZ2-O-Rf-A) (1) (In the formula, X's may be the same or different and each represent -H or F; Y's may be -H, -F, an alkyl group, or a fluorine-containing alkyl group; and Z's may be the same or different and each represent -H, -F, an alkyl group, or a fluoroalkyl group. Rf's each represent a fluorine-containing alkylene group having 1 to 40 carbon atoms, or a fluorine-containing alkylene group having 2 to 100 carbon atoms and an ether bond. A's each represent -COOM, -SO3M, -OSO3M, or -C(CF3)2OM (M's each represent -H, a metal atom, or -NR 7 4. An optionally substituted imidazolium, an optionally substituted pyridinium, or an optionally substituted phosphonium, wherein R 7 is H or an organic group.) However, at least one of X, Y, and Z contains a fluorine atom.)

[0110] In the production method of the present disclosure, the monomer (1) represented by general formula (1) may be copolymerized with other monomers. The polymer (1) may be a homopolymer of the monomer (1) represented by the general formula (1), or may be a copolymer with other monomers.

[0111] The fluorine-containing alkylene group having 2 to 100 carbon atoms and an ether bond is an alkylene group that does not contain a structure in which an oxygen atom is at the terminal and that contains an ether bond between carbon atoms.

[0112] In general formula (1), X is -H or F. Both Xs may be -F, or at least one X may be -H. For example, one X may be -F and the other may be -H, or both Xs may be -H.

[0113] In general formula (1), Y is -H, -F, an alkyl group, or a fluorine-containing alkyl group. The alkyl group is an alkyl group that does not contain a fluorine atom, and may have one or more carbon atoms. The alkyl group preferably has six or fewer carbon atoms, more preferably four or fewer carbon atoms, and even more preferably three or fewer carbon atoms. The fluorine-containing alkyl group is an alkyl group that contains at least one fluorine atom, and may have one or more carbon atoms. The fluorine-containing alkyl group preferably has six or fewer carbon atoms, more preferably four or fewer carbon atoms, and even more preferably three or fewer carbon atoms. Y is preferably -H, -F, or CF3, and more preferably -F.

[0114] In general formula (1), Z's may be the same or different and represent -H, -F, an alkyl group, or a fluoroalkyl group. The alkyl group is an alkyl group that does not contain a fluorine atom, and may have one or more carbon atoms. The alkyl group preferably has six or fewer carbon atoms, more preferably four or fewer carbon atoms, and even more preferably three or fewer carbon atoms. The fluorine-containing alkyl group is an alkyl group that contains at least one fluorine atom, and may have one or more carbon atoms. The fluorine-containing alkyl group preferably has six or fewer carbon atoms, more preferably four or fewer carbon atoms, and even more preferably three or fewer carbon atoms. Z's are preferably -H, -F, or CF3, and more preferably -F.

[0115] In general formula (1), at least one of X, Y, and Z contains a fluorine atom. For example, X may be —H, and Y and Z may be —F.

[0116] In the general formula (1), Rf is a fluorine-containing alkylene group having 1 to 40 carbon atoms or a fluorine-containing alkylene group having 2 to 100 carbon atoms and an ether bond.

[0117] The number of carbon atoms in the fluorine-containing alkylene group is preferably 2 or more. The number of carbon atoms in the fluorine-containing alkylene group is preferably 30 or less, more preferably 20 or less, even more preferably 10 or less, particularly preferably 6 or less, and most preferably 3 or less. Examples of the fluorine-containing alkylene group include -CF2-, -CH2CF2-, -CF2CF2-, -CF2CH2-, -CF2CF2CF2-, -CF2CF2CH2-, -CF(CF3)-, -CF(CF3)CF2-, and -CF(CF3)CH2-. The fluorine-containing alkylene group is preferably a perfluoroalkylene group.

[0118] The number of carbon atoms in the fluorine-containing alkylene group having an ether bond is preferably 3 or more. The number of carbon atoms in the fluorine-containing alkylene group having an ether bond is preferably 60 or less, more preferably 30 or less, even more preferably 12 or less, particularly preferably 9 or less, and most preferably 6 or less. The fluorine-containing alkylene group having an ether bond is, for example, a group represented by the general formula: [ka] (In the formula, Z 1 is F or CF3;Z 2 and Z 3 are H or F;Z respectively 4 is also preferably a divalent group represented by the formula: H, F, or CF3; p1+q1+r1 is an integer of 1 to 10; s1 is 0 or 1; and t1 is an integer of 0 to 5).

[0119] Specific examples of the fluorine-containing alkylene group having an ether bond include -CFCF(CF)OCF-, -CF(CF)CF-O-CF(CF)-, -(CF(CF)CF-O) n -CF(CF3)- (wherein n is an integer of 1 to 10), -CF(CF3)CF2-O-CF(CF3)CH2-, -(CF(CF3)CF2-O) nExamples include -CF(CF3)CH2- (wherein n is an integer of 1 to 10), -CH2CF2CF2O-CH2CF2CH2-, -CF2CF2CF2O-CF2-, -CF2CF2CF2O-CF2CF2-, -CF2CF2CF2O-CF2CF2-, -CF2CF2CF2O-CF2CF2CH2-, -CF2CF2O-CF2-, -CF2CF2O-CF2CH2-, etc. The fluorine-containing alkylene group having an ether bond is preferably a perfluoroalkylene group.

[0120] In the general formula (1), A is -COOM, -SO3M, -OSO3M, or -C(CF3)2OM (M is H, a metal atom, or NR 7 4. An optionally substituted imidazolium, an optionally substituted pyridinium, or an optionally substituted phosphonium, wherein R 7 is H or an organic group).

[0121] R 7 As for H or C 1-10 is preferably an organic group represented by the formula: 1-4 The organic group is more preferably H or C 1-4 More preferred are alkyl groups of the formula:

[0122] Examples of the metal atom include alkali metals (Group 1) and alkaline earth metals (Group 2), and Na, K or Li is preferred.

[0123] M is H, a metal atom, or NR 7 4 is preferred, H, an alkali metal (Group 1), an alkaline earth metal (Group 2) or NR 7 4 is more preferred, H, Na, K, Li or NH4 is even more preferred, H, Na, K or NH4 is even more preferred, H, Na or NH4 is especially preferred, and H or NH4 is most preferred.

[0124] A is preferably —COOM or —SO3M, and more preferably —COOM.

[0125] Examples of the monomer represented by general formula (1) include a monomer represented by general formula (1a): CX2=CFCF2-O-(CF(CF3)CF2O) n5 -CF(CF3)-A (1a) (wherein each X is the same and represents F or H, n5 represents 0 or an integer of 1 to 10, and A is as defined above) is exemplified.

[0126] In general formula (1a), n5 is preferably 0 or an integer of 1 to 5, more preferably 0, 1 or 2, and even more preferably 0 or 1, in that particles with a small primary particle size can be obtained.

[0127] In the production method of the present disclosure, the monomer represented by general formula (1a) may be copolymerized with other monomers. The polymer (1) may be a homopolymer of the monomer represented by the general formula (1a) or a copolymer with other monomers.

[0128] The monomer (1) is preferably a monomer represented by the general formula (1A). The polymerized unit (1) is preferably a polymerized unit (1A) based on a monomer represented by general formula (1A). CH2=CF(-CF2-O-Rf-A) (1A) (wherein Rf and A are the same as above.)

[0129] In the production method of the present disclosure, the monomer represented by general formula (1A) may be copolymerized with other monomers. The polymer (1) may be a homopolymer of the monomer represented by the general formula (1A) or a copolymer with other monomers.

[0130] Specific examples of the monomer represented by formula (1A) include the monomer represented by the general formula:

[0131] [ka]

[0132] (In the formula, Z 1 is F or CF3;Z 2 and Z 3 are H or F;Z respectively 4 is H, F, or CF3; p1+q1+r1 are integers from 0 to 10; s1 is 0 or 1; t1 is an integer from 0 to 5, except for Z 3 and Z 4 are both H, then p1+q1+r1+s1 is not 0; A is the same as defined above). More specifically,

[0133] [ka]

[0134] Among them,

[0135] [ka]

[0136] It is preferable that:

[0137] As the monomer represented by general formula (1A), it is preferable that A in formula (1A) is -COOM, and in particular, at least one selected from the group consisting of CH2=CFCF2OCF(CF3)COOM and CH2=CFCF2OCF(CF3)CF2OCF(CF3)COOM (wherein M is as defined above) is preferred, with CH2=CFCF2OCF(CF3)COOM being more preferred.

[0138] Further, examples of the monomer represented by the general formula (1) include the monomer represented by the following formula: CF2=CFCF2-O-Rf-A (wherein Rf and A are the same as above)

[0139] More specifically, [ka] etc.

[0140] The monomer (I) is also preferably a monomer (2) represented by the general formula (2). The polymer (I) is also preferably a polymer (2) containing polymerized units (2) based on a monomer represented by general formula (2). CX2=CY(-O-Rf-A) (2) (In the formula, X's are the same or different and represent -H or F; Y represents -H, -F, an alkyl group or a fluorine-containing alkyl group; Rf represents a fluorine-containing alkylene group having 1 to 40 carbon atoms or a fluorine-containing alkylene group having 2 to 100 carbon atoms and having an ether bond or a keto group; and A is the same as defined above.)

[0141] In the production method of the present disclosure, the monomer (2) represented by general formula (2) may be copolymerized with other monomers. The polymer (2) may be a homopolymer of the monomer represented by the general formula (2) or a copolymer with other monomers.

[0142] In general formula (2), X is -H or F. Both Xs may be -F, or at least one X may be -H. For example, one X may be -F and the other may be -H, or both Xs may be -H.

[0143] In general formula (2), Y is -H, -F, an alkyl group, or a fluorine-containing alkyl group. The alkyl group is an alkyl group that does not contain a fluorine atom, and may have one or more carbon atoms. The alkyl group preferably has six or fewer carbon atoms, more preferably four or fewer carbon atoms, and even more preferably three or fewer carbon atoms. The fluorine-containing alkyl group is an alkyl group that contains at least one fluorine atom, and may have one or more carbon atoms. The fluorine-containing alkyl group preferably has six or fewer carbon atoms, more preferably four or fewer carbon atoms, and even more preferably three or fewer carbon atoms. Y is preferably -H, -F, or CF3, and more preferably -F.

[0144] In general formula (2), it is preferable that at least one of X and Y contains a fluorine atom. For example, X may be —H, and Y and Z may be —F.

[0145] In general formula (2), Rf is a fluorine-containing alkylene group having 1 to 40 carbon atoms, a fluorine-containing alkylene group having an ether bond having 2 to 100 carbon atoms, or a fluorine-containing alkylene group having a keto group having 2 to 100 carbon atoms. The fluorine-containing alkylene group having an ether bond having 2 to 100 carbon atoms is an alkylene group that does not contain a structure in which an oxygen atom is at the terminal and that contains an ether bond between carbon atoms.

[0146] The number of carbon atoms in the fluorine-containing alkylene group of Rf is preferably 2 or more. Also, it is preferably 30 or less, more preferably 20 or less, even more preferably 10 or less, and particularly preferably 5 or less. Examples of the fluorine-containing alkylene group include -CF2-, -CH2CF2-, -CF2CF2-, -CF2CH2-, -CF2CF2CH2-, -CF(CF3)-, -CF(CF3)CF2-, -CF(CF3)CH2-, -CF2CF2CF2-, CF2CF2CF2CF2-, and the like. The fluorine-containing alkylene group is preferably a perfluoroalkylene group, and more preferably an unbranched linear perfluoroalkylene group.

[0147] The number of carbon atoms in the fluorine-containing alkylene group having an ether bond is preferably 3 or more. The number of carbon atoms in the fluorine-containing alkylene group having an ether bond is preferably 60 or less, more preferably 30 or less, even more preferably 12 or less, and particularly preferably 5 or less. The fluorine-containing alkylene group having an ether bond is, for example, a group represented by the general formula: [ka] (In the formula, Z 1 is F or CF3;Z 2 and Z 3 are H or F;Z respectively 4is also preferably a divalent group represented by the formula: H, F, or CF3; p1+q1+r1 is an integer of 1 to 10; s1 is 0 or 1; and t1 is an integer of 0 to 5).

[0148] Specific examples of the fluorine-containing alkylene group having an ether bond include -CF2CF(CF3)OCF2-, -CF2CF(CF3)OCF2CF2-, -CF2CF(CF3)OCF2CF2CF2-, -CF(CF3)CF2-O-CF(CF3)-, -(CF(CF3)CF2-O) n -CF(CF3)- (wherein n is an integer of 1 to 10), -CF(CF3)CF2-O-CF(CF3)CH2-, -(CF(CF3)CF2-O) n Examples include -CF(CF3)CH2- (wherein n is an integer of 1 to 10), -CH2CF2CF2O-CH2CF2CH2-, -CF2CF2CF2O-CF2-, -CF2CF2CF2O-CF2CF2-, -CF2CF2CF2O-CF2CF2-, -CF2CF2CF2O-CF2CF2CH2-, -CF2CF2O-CF2-, -CF2CF2O-CF2CH2-, etc. The fluorine-containing alkylene group having an ether bond is preferably a perfluoroalkylene group.

[0149] The carbon number of the fluorine-containing alkylene group having a keto group is preferably 3 or more. The carbon number of the fluorine-containing alkylene group having a keto group is preferably 60 or less, more preferably 30 or less, even more preferably 12 or less, and particularly preferably 5 or less.

[0150] Specific examples of the fluorine-containing alkylene group having a keto group include -CF2CF(CF3)CO-CF2-, -CF2CF(CF3)CO-CF2CF2-, -CF2CF(CF3)CO-CF2CF2CF2-, -CF2CF(CF3)CO-CF2CF2CF2-, etc. The fluorine-containing alkylene group having a keto group is preferably a perfluoroalkylene group.

[0151] Water may be added to the keto group in the fluorine-containing alkylene group. Therefore, the monomer (2) may be a hydrate. Examples of the fluorine-containing alkylene group in which water is added to the keto group include -CFCF(CF)C(OH)-CF-, -CFCF(CF)C(OH)-CFCF-, -CFCF(CF)C(OH)-CFCFCF-, and -CFCF(CF)C(OH)-CFCFCFCF-.

[0152] The monomer represented by general formula (2) is preferably at least one selected from the group consisting of monomers represented by general formulas (2a), (2b), (2c), (2d) and (2e). CF2=CF-O-(CF2) n1 -A (2a) (wherein n1 represents an integer of 1 to 10, and A is the same as defined above.) CF2=CF-O-(CF2C(CF3)F) n2 -A (2b) (wherein n2 represents an integer of 1 to 5, and A is as defined above.) CF2=CF-O-(CFX 1 ) n3 -A (2c) (In the formula, X 1 represents F or CF3, n3 represents an integer of 1 to 10, and A is as defined above. CF2=CF-O-(CF2CFX 1 O) n4 -(CF2) n6 -A (2d) (wherein n4 represents an integer of 1 to 10, n6 represents an integer of 1 to 3, and A and X 1 is the same as the definition above.) CF2=CF-O-(CF2CF2CFX 1 O) n5 -CF2CF2CF2-A (2e) (wherein n5 represents an integer of 0 to 10, and A and X 1 is the same as the definition above.)

[0153] In the general formula (2a), n1 is preferably an integer of 5 or less, and more preferably an integer of 2 or less.

[0154] Examples of the monomer represented by general formula (2a) include CF2=CF-O-CF2COOM, CF2=CF(OCF2CF2COOM), CF2=CF(O(CF2)3COOM), CF2=CF(OCF2CF2SO3M), CF2=CFOCF2SO3M, and CF2=CFOCF2CF2CF2SO3M (wherein M is as defined above).

[0155] In general formula (2b), n2 is preferably an integer of 3 or less, from the viewpoint of the dispersion stability of the resulting composition.

[0156] In general formula (2c), n3 is preferably an integer of 5 or less from the viewpoint of water solubility, A is preferably -COOM, and M is preferably H, Na, or NH4.

[0157] In general formula (2d), X 1 is preferably -CF3 from the viewpoint of dispersion stability of the composition, n4 is preferably an integer of 5 or less from the viewpoint of water solubility, A is preferably -COOM, and M is preferably H, Na, or NH4.

[0158] Examples of the monomer represented by general formula (2d) include CF2=CFOCF2CF(CF3)OCF2CF2COOM, CF2=CFOCF2CF(CF3)OCF2COOM, CF2=CFOCF2CF(CF3)OCF2CF2CF2COOM, CF2=CFOCF2CF(CF3)OCF2CF2CF2COOM, CF2=CFOCF2CF(CF3)OCF2SO3M, CF2=CFOCF2CF(CF3)OCF2CF2SO3M, CF2=CFOCF2CF(CF3)OCF2CF2CF2SO3M (wherein M represents H, NH4 or an alkali metal).

[0159] In general formula (2e), n5 is preferably an integer of 5 or less from the viewpoint of water solubility, A is preferably -COOM, and M is preferably H, Na or NH4.

[0160] Examples of the monomer represented by general formula (2e) include CF2=CFOCF2CF2CF2COOM (wherein M represents H, NH4 or an alkali metal).

[0161] The monomer (I) is also preferably a monomer (3) represented by the general formula (3). The polymer (I) is also preferably a polymer (3) containing polymerized units (3) based on a monomer represented by general formula (3). CX2=CY(-Rf-A) (3) (In the formula, X's are the same or different and represent -H or F; Y represents -H, -F, an alkyl group or a fluorine-containing alkyl group; Rf represents a fluorine-containing alkylene group having 1 to 40 carbon atoms or a fluorine-containing alkylene group having an ether bond having 2 to 100 carbon atoms; and A is the same as defined above.)

[0162] In the production method of the present disclosure, the monomer (3) represented by general formula (3) may be copolymerized with other monomers. The polymer (3) may be a homopolymer of the monomer represented by the general formula (3) or a copolymer with other monomers.

[0163] The fluorine-containing alkylene group having 2 to 100 carbon atoms and an ether bond is an alkylene group that does not contain a structure in which an oxygen atom is at the terminal and that contains an ether bond between carbon atoms.

[0164] In general formula (3), Rf is preferably a fluorine-containing alkylene group having a carbon number of 1 to 40. In general formula (3), at least one of X and Y preferably contains a fluorine atom.

[0165] The monomer represented by general formula (3) is represented by general formula (3a): CF2=CF-(CF2)n1 -A (3a) (wherein n1 represents an integer of 1 to 10, and A is as defined above), and a monomer represented by general formula (3b): CF2=CF-(CF2C(CF3)F) n2 -A (3b) (wherein n2 represents an integer of 1 to 5, and A is as defined above), is preferred.

[0166] In the general formula (3a) and the general formula (3b), A is preferably —SO3M or COOM, and M is H, a metal atom, NR 7 4. It is preferably an imidazolium which may have a substituent, a pyridinium which may have a substituent, or a phosphonium which may have a substituent. 7 represents H or an organic group.

[0167] In general formula (3a), n1 is preferably an integer of 5 or less, more preferably an integer of 2 or less. A is preferably -COOM, and M is preferably H or NH4.

[0168] An example of the monomer represented by general formula (3a) is CF2=CFCF2COOM (wherein M is as defined above).

[0169] In general formula (3b), n2 is preferably an integer of 3 or less from the viewpoint of dispersion stability of the resulting composition, A is preferably -COOM, and M is preferably H or NH4.

[0170] Next, a preferred configuration when m in general formula (I) is an integer of 2 or more will be described.

[0171] It is also preferable that the monomer (I) is at least one selected from the group consisting of monomers represented by general formula (4a) and general formula (4b). It is also preferable that the polymer (I) is a polymer (4) containing polymerization units (4) based on at least one monomer selected from the group consisting of monomers represented by general formula (4a) and general formula (4b). CF2=CF-CF2-OQ F1 -CF(-Q F2 -CZ 1 Z 2 -A)2(4a) (In the formula, Z 1 , Z 2 and A are the same as above, Q F1 and Q F2 are the same or different and are a single bond, a fluorine-containing alkylene group which may contain an ether bond between carbon atoms, or a fluorine-containing oxyalkylene group which may contain an ether bond between carbon atoms. CF2=CF-OQ F1 -CF(-Q F2 -CZ 1 Z 2 -A)2(4b) (In the formula, Z 1 , Z 2 , A, Q F1 and Q F2 is the same as above)

[0172] The monomers represented by general formula (4a) and general formula (4b) include: [ka] etc.

[0173] As the monomer (I), at least one selected from the group consisting of the monomer (1), the monomer (2) and the monomer (3) is preferred, the monomer (1) is more preferred, and the monomer (1A) is even more preferred. The polymer (I) is preferably at least one selected from the group consisting of polymer (1), polymer (2) and polymer (3), and more preferably polymer (1).

[0174] In the production method of the present disclosure, the monomer (I) may be copolymerized with other monomers. The polymer (I) may be a homopolymer consisting of only the polymerized unit (I), or may be a copolymer containing the polymerized unit (I) and a polymerized unit based on another monomer copolymerizable with the monomer represented by general formula (I). From the viewpoint of solubility in an aqueous medium, a homopolymer consisting of only the polymerized unit (I) is preferred. The polymerized units (I) may be the same or different in each occurrence, and the polymer (I) may contain polymerized units (I) based on two or more different monomers represented by general formula (I).

[0175] The other monomer is preferably a monomer represented by the general formula CFR=CR2 (wherein R is independently H, F, or a perfluoroalkyl group having 1 to 4 carbon atoms). Fluorine-containing ethylenic monomers having 2 or 3 carbon atoms are also preferred. Examples of the other monomer include CF2=CF2, CF2=CFCl, CH2=CF2, CFH=CH2, CFH=CF2, CF2=CFCF3, CH2=CFCF3, CH2=CHCF3, CHF=CHCF3 (E-form), CHF=CHCF3 (Z-form), and CHF=CHF. Among these, at least one selected from the group consisting of tetrafluoroethylene (CF2=CF2), chlorotrifluoroethylene (CF2=CFCl) and vinylidene fluoride (CH2=CF2) is preferred in terms of good copolymerizability, with tetrafluoroethylene being more preferred. Therefore, the polymerized units based on the other monomer are preferably polymerized units based on tetrafluoroethylene. The polymerized units based on the other monomers may be the same or different in each occurrence, and the polymer (I) may contain polymerized units based on two or more different types of other monomers.

[0176] The other monomers also include those represented by the general formula (n1-2):

[0177] [ka]

[0178] (In the formula, X 1 , X 2are the same or different H or F;X 3 is H, F, Cl, CH3 or CF3; X 4 , X 5 are the same or different and are H or F; a and c are the same or different and are 0 or 1. Rf 3 is a fluorine-containing alkyl group having 1 to 40 carbon atoms or a fluorine-containing alkyl group having 2 to 100 carbon atoms and having an ether bond).

[0179] Specifically, CH2=CFCF2-O-Rf 3 , CF2=CF-O-Rf 3 , CF2=CFCF2-O-Rf 3 , CF2=CF-Rf 3 , CH2=CH-Rf 3 , CH2=CH-O-Rf 3 (In the formula, Rf 3 is the same as the above formula (n1-2)).

[0180] Examples of the other monomers include those of formula (n2-1):

[0181] [ka]

[0182] (In the formula, X 9 is H, F or CH3; Rf 4 Also included are fluorine-containing acrylate monomers represented by Rf (a fluorine-containing alkyl group having 1 to 40 carbon atoms or a fluorine-containing alkyl group having 2 to 100 carbon atoms and an ether bond). 4 The base is

[0183] [ka]

[0184] (wherein d3 is an integer of 1 to 4; e3 is an integer of 1 to 10).

[0185] Examples of the other monomers include those of formula (n2-2): CH2=CHO-Rf 5 (n2-2) (In the formula, Rf 5 is a fluorine-containing alkyl group having 1 to 40 carbon atoms or a fluorine-containing alkyl group having 2 to 100 carbon atoms and having an ether bond).

[0186] Specific examples of the monomer of general formula (n2-2) include:

[0187] [ka]

[0188] (wherein e6 is an integer of 1 to 10) are preferred.

[0189] More specifically,

[0190] [ka]

[0191] Examples include:

[0192] Others include those of general formula (n2-3): CH2=CHCH2O-Rf 6 (n2-3) (In the formula, Rf 6 is a fluorine-containing alkyl group having 1 to 40 carbon atoms or a fluorine-containing alkyl group having 2 to 100 carbon atoms and having an ether bond), a fluorine-containing allyl ether represented by the general formula (n2-4): CH2=CH-Rf 7 (n2-4) (In the formula, Rf 7 is a fluorine-containing alkyl group having 1 to 40 carbon atoms or a fluorine-containing alkyl group having 2 to 100 carbon atoms and having an ether bond), and the like.

[0193] Specific examples of the monomers represented by general formulas (n2-3) and (n2-4) include:

[0194] [ka]

[0195] Examples of such monomers include:

[0196] In the polymer (I), the content of the polymerized units (I) relative to all polymerized units is, in order of preference, 1.0 mol% or more, 3.0 mol% or more, 5.0 mol% or more, 10 mol% or more, 20 mol% or more, 30 mol% or more, 40 mol% or more, 50 mol% or more, 60 mol% or more, 70 mol% or more, 80 mol% or more, and 90 mol% or more. The content of the polymerized units (I) is particularly preferably substantially 100 mol%, and the polymer (I) is most preferably composed only of the polymerized units (I).

[0197] In polymer (I), the content of polymerized units based on other monomers copolymerizable with the monomer represented by general formula (I) is, in order of preference, 99.0 mol% or less, 97.0 mol% or less, 95.0 mol% or less, 90 mol% or less, 80 mol% or less, 70 mol% or less, 60 mol% or less, 50 mol% or less, 40 mol% or less, 30 mol% or less, 20 mol% or less, and 10 mol% or less, based on all polymerized units. It is particularly preferred that the content of polymerized units based on other monomers copolymerizable with the monomer represented by general formula (I) is substantially 0 mol%, and it is most preferred that polymer (I) does not contain polymerized units based on other monomers.

[0198] The lower limit of the weight average molecular weight (Mw) of the polymer (I) is, in order of preference, 0.2×10 4 That's 0.4 x 10 4 That's 0.6 x 10 4 That's 0.8 x 10 4 That's it, 1.0 x 10 4 That's it, 1.3 x 10 4 That's it, 1.4 x 10 4 That's it, 1.5 x 10 4 That's 1.7 x 10 4 That's it, 1.9 x 10 4 That's it, 2.1 x 104 That's it, 2.3 x 10 4 That's it, 2.7 x 10 4 That's it, 3.1 x 10 4 That's it, 3.5 x 10 4 That's it, 3.9 x 10 4 That's it, 4.3 x 10 4 The upper limit of the weight average molecular weight (Mw) of the polymer (I) is, in order of preference, 150.0×10 4 Below, 100.0 x 10 4 Below, 60.0 x 10 4 Below, 50.0 x 10 4 Below, 40.0 x 10 4 The following is the result.

[0199] The lower limit of the number average molecular weight (Mn) of the polymer (I) is, in order of preference, 0.1 × 10 4 Above, 0.2 × 10 4 Above, 0.3 × 10 4 That's 0.4 x 10 4 Above, 0.5 x 10 4 That's it, 1.0 x 10 4 That's it, 1.2 x 10 4 That's it, 1.4 x 10 4 That's it, 1.6 x 10 4 That's it, 1.8 x 10 4 The upper limit of the number average molecular weight (Mn) of the polymer (I) is, in order of preference, 75.0 × 10 4 Below, 50.0 x 10 4 Below, 40.0 x 10 4 Below, 30.0 x 10 4 Below, 20.0 x 10 4 The following is the result.

[0200] The molecular weight distribution (Mw / Mn) of the polymer (I) is preferably 3.0 or less, 2.4 or less, 2.2 or less, 2.0 or less, 1.9 or less, 1.7 or less, 1.5 or less, 1.4 or less, and 1.3 or less.

[0201] The number average molecular weight and weight average molecular weight are values ​​calculated by gel permeation chromatography (GPC) using monodisperse polystyrene as a standard. When GPC measurement is not possible, the number average molecular weight of polymer (I) can be determined from the correlation between the number average molecular weight calculated from the number of terminal groups obtained by NMR, FT-IR, etc. and the melt flow rate. The melt flow rate can be measured in accordance with JIS K 7210.

[0202] The polymer (I) typically has terminal groups. The terminal groups are generated during polymerization, and typical terminal groups are independently selected from hydrogen, iodine, bromine, linear or branched alkyl groups, and linear or branched fluoroalkyl groups, and may optionally contain at least one catenary heteroatom. The alkyl or fluoroalkyl group preferably has 1 to 20 carbon atoms. These terminal groups are generally generated from the initiator or chain transfer agent used to form the polymer (I), or are generated during the chain transfer reaction.

[0203] Preferably, polymer (I) has an ion exchange ratio (IXR) of 53 or less, where IXR is defined as the number of carbon atoms in the polymer backbone relative to the ionic group. Precursor groups that become ionic upon hydrolysis (e.g., -SOF) are not considered ionic groups for purposes of determining IXR.

[0204] IXR is preferably 0.5 or more, more preferably 1 or more, even more preferably 3 or more, even more preferably 4 or more, particularly preferably 5 or more, and particularly preferably 8 or more. IXR is more preferably 43 or less, more preferably 33 or less, and particularly preferably 23 or less.

[0205] The ion exchange capacity of the polymer (I) is, in order of preference, 0.80 meq / g or more, 1.50 meq / g or more, 1.75 meq / g or more, 2.00 meq / g or more, 2.50 meq / g or more, 2.60 meq / g or more, 3.00 meq / g or more, and 3.50 meq / g or more. The ion exchange capacity is the content of ionic groups (anionic groups) in the polymer (I) and is calculated from the composition of the polymer (I).

[0206] In polymer (I), the ionic (anionic) groups are typically distributed along the polymer backbone. The polymer (I) comprises a polymer backbone with recurring side chains attached to the backbone, which preferably carry ionic groups.

[0207] Preferably, polymer (I) comprises ionic groups having a pKa of less than 10, more preferably less than 7. The ionic groups of polymer (I) are preferably selected from the group consisting of sulfonate, carboxylate, phosphonate, and phosphate.

[0208] The terms "sulfonate, carboxylate, phosphonate, and phosphate" are intended to refer to the respective salts or the respective acids capable of forming salts. When salts are used, preferably the salts are alkali metal or ammonium salts. A preferred ionic group is a sulfonate group.

[0209] The polymer (I) is preferably water-soluble. Water-soluble means the property of being easily dissolved or dispersed in an aqueous medium. The particle size of the water-soluble polymer (I) cannot be measured by dynamic light scattering (DLS), for example, or the particle size is 10 nm or less.

[0210] The polymer (I) preferably has sufficient water solubility. Generally, the higher the content of the polymer (I) in the aqueous solution, the more difficult it becomes for the polymer (I) to be sufficiently dissolved or dispersed in the aqueous medium. Therefore, even when the content of the polymer (I) in the aqueous solution is high, if the particle size of the polymer (I) cannot be measured by dynamic light scattering (DLS), it can be said to be highly water soluble. It is preferable that the particle size of the polymer (I) cannot be measured even when it is contained in an aqueous solution at a content of 1.0% by mass. It is more preferable that the particle size of the polymer (I) cannot be measured even when it is contained in an aqueous solution at a content of 1.5% by mass, and even more preferably at a content of 2.0% by mass.

[0211] The viscosity of an aqueous solution of polymer (I) is preferably 5.0 mPa s or more, more preferably 8.0 mPa s or more, even more preferably 10.0 mPa s or more, particularly preferably 12.0 mPa s or more, and most preferably 14.0 mPa s or more, and preferably 100.0 mPa s or less, more preferably 50.0 mPa s or less, even more preferably 25.0 mPa s or less, and especially preferably 20.0 mPa s or less.

[0212] The viscosity of an aqueous solution of polymer (I) can be determined by adjusting the content of polymer (I) in the aqueous solution to 33 mass % based on the amount of the aqueous solution, and measuring the viscosity of the resulting aqueous solution at 20°C using a tuning fork vibro viscometer (model number: SV-10) manufactured by A&D Corporation.

[0213] The critical micelle concentration (CMC) of the polymer (I) is preferably 0.1% by mass or more, more preferably 0.5% by mass or more, even more preferably 1% by mass or more, and preferably 20% by mass or less, more preferably 10% by mass or less, even more preferably 5% by mass or less.

[0214] The critical micelle concentration of the polymer (I) can be determined by measuring the surface tension, for example, using a surface tensiometer CBVP-A3 manufactured by Kyowa Interface Science Co., Ltd.

[0215] The acid value of the polymer (I) is preferably 60 or more, more preferably 90 or more, even more preferably 120 or more, particularly preferably 150 or more, and most preferably 180 or more. The upper limit is not particularly limited, but is preferably 300 or less.

[0216] The acid value of the polymer (I) is determined by the presence of an anionic group other than an acid functional group, such as -COOM, -SO3M, -OSO3M, or -C(CF3)2OM (where M is a metal atom, NR 7 4. An optionally substituted imidazolium, an optionally substituted pyridinium, or an optionally substituted phosphonium, wherein R 7 If the compound has a hydroxyl group (H or an organic group), these groups can be converted to acid forms and then measured by acid-base titration.

[0217] The polymer (I) is a polymer (11) of a monomer (11) represented by general formula (11), in which the content of polymerized units (11) based on the monomer (11) is 50 mol% or more based on all polymerized units constituting the polymer (11), and the weight average molecular weight (Mw) is 38.0 × 10 4 The polymer (11) described above can also be used. The polymer (11) is a novel polymer. General formula (11): CX2=CY-CF2-O-Rf-A (In the formula, X and Y are independently H, F, CH3 or CF3, and at least one of X and Y is F. Rf is a fluorine-containing alkylene group having 1 to 40 carbon atoms or a fluorine-containing alkylene group having 2 to 100 carbon atoms and an ether bond. A is -COOM, -SO3M, -OSO3M or -C(CF3)2OM (M is H, a metal atom, NR 7 4. An optionally substituted imidazolium, an optionally substituted pyridinium, or an optionally substituted phosphonium, wherein R 7 is H or an organic group.

[0218] In general formula (11), X and Y are independently H, F, CH3, or CF3, and at least one of X and Y is F. X is preferably H or F, and more preferably H. Y is preferably H or F, and more preferably F.

[0219] Rf and A in the general formula (11) are the same as Rf and A in the general formula (1) representing the monomer constituting the polymer (1).

[0220] The polymer (11) may be a homopolymer consisting of only polymerized units (11) based on the monomer (11), or may be a copolymer containing polymerized units (11) and polymerized units based on other monomers copolymerizable with the monomer (11). The other monomers are as described above. The polymerized units (11) may be the same or different in each occurrence, and the polymer (11) may contain polymerized units (11) based on two or more different monomers represented by the general formula (11).

[0221] The content of the polymerized units (11) in the polymer (11) is, in order of preference, 50 mol % or more, 60 mol % or more, 70 mol % or more, 80 mol % or more, 90 mol % or more, and 99 mol % or more of all the polymerized units constituting the polymer (11). The content of the polymerized units (11) is particularly preferably substantially 100 mol %, and the polymer (11) is most preferably composed solely of the polymerized units (11).

[0222] In polymer (11), the content of polymerized units based on other monomers copolymerizable with monomer (11) is, in order of preference, 99.0 mol% or less, 97.0 mol% or less, 95.0 mol% or less, 90 mol% or less, 80 mol% or less, 70 mol% or less, 60 mol% or less, and 50 mol% or less, based on all polymerized units constituting polymer (11). It is particularly preferred that the content of polymerized units based on other monomers copolymerizable with monomer (11) is substantially 0 mol%, and it is most preferred that polymer (11) does not contain polymerized units based on other monomers.

[0223] The lower limit of the weight average molecular weight of the polymer (11) is, in order of preference, 38.0×10 4 That's it, 40.0 x 10 4 The upper limit of the weight average molecular weight of the polymer (11) is, in order of preference, 150.0×10 4 Below, 100.0 x 10 4 Below, 60.0 x 10 4 is.

[0224] The lower limit of the number average molecular weight of the polymer (11) is, in order of preference, 5.0 × 10 4 , 8.0×10 4 , 10.0×10 4 That's it, 12.0 x 10 4 The upper limit of the number average molecular weight of the polymer (11) is, in order of preference, 75.0 × 10 4 Below, 50.0 x 10 4 Below, 40.0 x 10 4 Below, 30.0 x 10 4 The following is the result.

[0225] The polymer (I) is a polymer (12) of a monomer (12) represented by general formula (12), in which the content of polymerized units (12) based on the monomer (12) is 50 mol % or more based on all polymerized units constituting the polymer (12), and the weight average molecular weight (Mw) is 1.4 × 10 4 The polymer (12) described above can also be used. The polymer (12) is a novel polymer. General formula (12): CX2=CX-O-Rf-A (In the formula, X is independently F or CF3, Rf is a fluorine-containing alkylene group having 1 to 40 carbon atoms, or a fluorine-containing alkylene group having 2 to 100 carbon atoms and an ether bond or a keto group, A is -COOM, -SO3M, -OSO3M, or -C(CF3)2OM (M is -H, a metal atom, -NR 7 4. An optionally substituted imidazolium, an optionally substituted pyridinium, or an optionally substituted phosphonium, wherein R 7 is H or an organic group.

[0226] In general formula (12), X is independently F or CF3. It is preferable that at least one X is F, and it is more preferable that all X are F.

[0227] Rf and A in the general formula (12) are the same as Rf and A in the general formula (2) representing the monomer constituting the polymer (2).

[0228] The polymer (12) may be a homopolymer consisting of only polymerized units (12) based on the monomer (12), or may be a copolymer containing polymerized units (12) and polymerized units based on other monomers copolymerizable with the monomer (12). The other monomers are as described above. The polymerized units (12) may be the same or different in each occurrence, and the polymer (12) may contain polymerized units (12) based on two or more different monomers represented by the general formula (12).

[0229] The content of the polymerized units (12) in the polymer (12) is, in order of preference, 50 mol % or more, 60 mol % or more, 70 mol % or more, 80 mol % or more, 90 mol % or more, and 99 mol % or more of all the polymerized units constituting the polymer (12). The content of the polymerized units (12) is particularly preferably substantially 100 mol %, and the polymer (12) is most preferably composed solely of the polymerized units (12).

[0230] In polymer (12), the content of polymerized units based on other monomers copolymerizable with monomer (12) is, in order of preference, 50 mol % or less, 40 mol % or less, 30 mol % or less, 20 mol % or less, 10 mol % or less, and 1 mol % or less, based on all polymerized units constituting polymer (12). It is particularly preferred that the content of polymerized units based on other monomers copolymerizable with monomer (12) is substantially 0 mol %, and it is most preferred that polymer (12) does not contain polymerized units based on other monomers.

[0231] The lower limit of the weight average molecular weight (Mw) of the polymer (12) is, in order of preference, 1.4×10 4That's 1.7 x 10 4 That's 1.9 x 10 4 That's it, 2.1 x 10 4 That's it, 2.3 x 10 4 That's it, 2.7 x 10 4 That's it, 3.1 x 10 4 That's it, 3.5 x 10 4 That's it, 3.9 x 10 4 That's it, 4.3 x 10 4 That's it, 4.7 x 10 4 That's it, 5.1 x 10 4 The upper limit of the weight average molecular weight (Mw) of the polymer (12) is, in order of preference, 150.0×10 4 Below, 100.0 x 10 4 Below, 60.0 x 10 4 Below, 50.0 x 10 4 Below, 40.0 x 10 4 The following is the result.

[0232] The lower limit of the number average molecular weight (Mn) of the polymer (12) is, in order of preference, 0.7×10 4 That's 0.9 x 10 4 That's it, 1.0 x 10 4 That's it, 1.2 x 10 4 That's it, 1.4 x 10 4 That's it, 1.6 x 10 4 That's it, 1.8 x 10 4 The upper limit of the number average molecular weight (Mn) of the polymer (12) is, in order of preference, 75.0×10 4 Below, 50.0 x 10 4 Below, 40.0 x 10 4 Below, 30.0 x 10 4 Below, 20.0 x 10 4 The following is the result.

[0233] The molecular weight distribution (Mw / Mn) of the polymer (12) is preferably 3.0 or less, more preferably 2.4 or less, even more preferably 2.2 or less, particularly preferably 2.0 or less, and most preferably 1.9 or less.

[0234] As the polymer (I), a polymer (13) of a monomer (13) represented by general formula (13) can be used, in which the content of polymerized units (13) based on the monomer (13) is 50 mass % or more of the total polymerized units constituting the polymer (13). The polymer (13) is a novel polymer. General formula (13): CX2=CX-O-Rf-SO3M (In the formula, X is independently F or CF3, Rf is a fluorine-containing alkylene group having 1 to 40 carbon atoms or a fluorine-containing alkylene group having 2 to 100 carbon atoms and having an ether bond or a keto group, M is —H, a metal atom, —NR 7 4. An optionally substituted imidazolium, an optionally substituted pyridinium, or an optionally substituted phosphonium, wherein R 7 is H or an organic group.

[0235] In general formula (13), X is independently F or CF3. It is preferable that at least one X is F, and it is more preferable that all X are F.

[0236] Rf and M in the general formula (13) are the same as Rf and A in the general formula (2) representing the monomer constituting the polymer (2).

[0237] The polymer (13) may be a homopolymer consisting of only polymerized units (13) based on the monomer (13), or may be a copolymer containing polymerized units (13) and polymerized units based on other monomers copolymerizable with the monomer (13). The other monomers are as described above. The polymerized units (13) may be the same or different in each occurrence, and the polymer (13) may contain polymerized units (13) based on two or more different monomers represented by the general formula (13).

[0238] The content of polymerized units (13) based on monomer (13) in polymer (13) is 50% by mass or more relative to all polymerized units constituting polymer (13). The content of polymerized units (13) in polymer (13) is, in order of preference, 50% by mass or more, 60% by mass or more, 70% by mass or more, 80% by mass or more, 90% by mass or more, and 99% by mass or more relative to all polymerized units constituting polymer (13). It is particularly preferable that the content of polymerized units (13) is substantially 100% by mass, and it is most preferable that polymer (13) consists solely of polymerized units (13).

[0239] In polymer (13), the content of polymerized units based on other monomers copolymerizable with monomer (13) is, in order of preference, 50% by mass or less, 40% by mass or less, 30% by mass or less, 20% by mass or less, 10% by mass or less, and 1% by mass or less, based on all polymerized units constituting polymer (13). It is particularly preferred that the content of polymerized units based on other monomers copolymerizable with monomer (13) is substantially 0% by mass, and it is most preferred that polymer (13) does not contain polymerized units based on other monomers.

[0240] The lower limit of the number average molecular weight of the polymer (13) is, in order of preference, 0.3 × 10 4 That's 0.4 x 10 4 Above, 0.5 x 10 4 That's 0.7 x 10 4 That's 0.8 x 10 4 That's it, 1.0 x 10 4 That's it, 1.2 x 10 4 That's it, 1.4 x 10 4 , 1.6×10 4 That's it, 1.8 x 10 4 That's it, 2.0 x 10 4 That's it, 3.0 x 10 4 The upper limit of the number average molecular weight of the polymer (13) is, in order of preference, 75.0 × 10 4 Below, 50.0 x 10 4 Below, 40.0 x 10 4 Below, 30.0 x 10 4 Below, 20.0 x 10 4 The following is the result.

[0241] The lower limit of the weight average molecular weight of the polymer (13) is, in order of preference, 0.4×10 4 Above, 0.5 x 10 4 That's 0.6 x 10 4 That's 0.8 x 10 4 That's it, 1.0 x 10 4 That's it, 1.2 x 10 4 That's it, 1.4 x 10 4 That's 1.7 x 10 4 That's it, 1.9 x 10 4 That's it, 2.1 x 10 4 That's it, 2.3 x 10 4 That's it, 2.7 x 10 4 That's it, 3.1 x 10 4 That's it, 3.5 x 10 4 That's it, 3.9 x 10 4 That's it, 4.3 x 10 4 That's it, 4.7 x 10 4 That's it, 5.1 x 10 4 That's it, 10.0 x 10 4 That's it, 15.0 x 10 4 That's it, 20.0 x 10 4 That's it, 25.0 x 10 4 The upper limit of the weight average molecular weight of the polymer (13) is, in order of preference, 150.0×10 4 Below, 100.0 x 10 4 Below, 60.0 x 10 4 Below, 50.0 x 10 4 Below, 40.0 x 10 4 The following is the result.

[0242] The molecular weight distribution (Mw / Mn) of the polymer (13) is preferably 3.0 or less, 2.4 or less, 2.2 or less, 2.0 or less, 1.9 or less, 1.7 or less, 1.5 or less, 1.4 or less, and 1.3 or less.

[0243] The polymer (I) can be produced by a conventionally known method except for using the above-mentioned monomers.

[0244] Among the polymers (I), the polymer (11) is a novel polymer, and can be produced by a production method (11) in which a monomer (11) represented by general formula (11) is polymerized in an aqueous medium to produce a polymer (11) of the monomer (11), and the production method (11) maintains the oxygen concentration in the polymerization reaction system at 500 ppm by volume or less.

[0245] In the production method (11), the oxygen concentration in the polymerization reaction system is 500 ppm by volume or less. In the production method (11), the oxygen concentration in the reaction system is maintained at 500 ppm by volume or less throughout the entire polymerization period of the monomer (11). The oxygen concentration in the reaction system is preferably 350 ppm by volume or less, more preferably 300 ppm by volume or less, even more preferably 100 ppm by volume or less, and particularly preferably 50 ppm by volume or less. In addition, the oxygen concentration in the reaction system is usually 0.01 ppm by volume or more.

[0246] In the production method (11), the polymerization temperature of the monomer (11) is preferably 59°C or lower, more preferably 57°C or lower, even more preferably 55°C or lower, and particularly preferably 53°C or lower, because a polymer (11) having a higher molecular weight can be easily produced. The polymerization temperature is preferably 20°C or higher, more preferably 25°C or higher, even more preferably 30°C or higher, and particularly preferably 35°C or higher.

[0247] In the production method (11), the monomer (11) may be copolymerized with the other monomers described above.

[0248] In the production method (11), the polymerization pressure is usually from atmospheric pressure to 10 MPaG, and is appropriately determined depending on the type of monomer used, the molecular weight of the target polymer, and the reaction rate.

[0249] In the production method (11), the polymerization time is usually 1 to 200 hours, and may be 5 to 100 hours.

[0250] Among the polymers (I), the polymer (12) is a novel polymer, and can be produced by a production method (12) for producing a polymer (12) from the monomer (12) by polymerizing the monomer (12) represented by the general formula (12) in an aqueous medium, wherein the oxygen concentration in the polymerization reaction system is maintained at 1500 ppm by volume or less.

[0251] In the production method (12), the oxygen concentration in the polymerization reaction system is 1500 ppm by volume or less. In the production method (12), the oxygen concentration in the reaction system is maintained at 1500 ppm by volume or less throughout the entire polymerization period of the monomer (12). The oxygen concentration in the reaction system is preferably 500 ppm by volume or less, more preferably 100 ppm by volume or less, and even more preferably 50 ppm by volume or less. In addition, the oxygen concentration in the reaction system is usually 0.01 ppm by volume or more.

[0252] Among the polymers (I), the polymer (13) is a novel polymer, and can be produced by a method (13) for producing a polymer (13) by polymerizing a monomer (13) represented by general formula (13) in an aqueous medium to produce a polymer (13) of the monomer (13).

[0253] In the production method (13), the oxygen concentration in the polymerization reaction system is preferably 1500 volume ppm or less, more preferably 500 volume ppm or less, even more preferably 100 volume ppm or less, and particularly preferably 50 volume ppm or less. The oxygen concentration in the reaction system is usually 0.01 volume ppm or more. In the above production method, it is preferred that the oxygen concentration in the reaction system be maintained within the above range throughout the entire polymerization period of the monomer (13).

[0254] In the production methods (12) and (13), the polymerization temperature of the monomers (12) and (13) is preferably 70°C or lower, more preferably 65°C or lower, even more preferably 60°C or lower, particularly preferably 55°C or lower, even more preferably 50°C or lower, particularly preferably 45°C or lower, most preferably 40°C or lower, preferably 10°C or higher, more preferably 15°C or higher, and even more preferably 20°C or higher, since this facilitates the production of polymers (12) and (13) having higher molecular weights.

[0255] In the production method (12) and the production method (13), the monomer (12) or the monomer (13) may be copolymerized with the other monomers described above.

[0256] In the production methods (12) and (13), the polymerization pressure is usually atmospheric pressure to 10 MPaG and is appropriately determined depending on the type of monomer used, the molecular weight of the target polymer, and the reaction rate.

[0257] In the production method (12) and the production method (13), the polymerization time is usually 1 to 200 hours, and may be 5 to 100 hours.

[0258] In the production methods (11) to (13), the oxygen concentration in the polymerization reaction system can be controlled, for example, by flowing an inert gas such as nitrogen or argon, or, when a gaseous monomer is used, the gaseous monomer, through the liquid or gas phase in the reactor. The oxygen concentration in the polymerization reaction system can be determined by measuring and analyzing the gas coming out of the exhaust gas line of the polymerization system with a low-concentration oxygen analyzer.

[0259] In the production methods (11) to (13), the aqueous medium is a reaction medium for polymerization and refers to a liquid containing water. The aqueous medium is not particularly limited as long as it contains water, and may contain water and, for example, a fluorine-free organic solvent such as an alcohol, ether, or ketone, and / or a fluorine-containing organic solvent having a boiling point of 40°C or lower. Water is preferred as the aqueous medium.

[0260] In the production methods (11) to (13), the polymerization of the monomers can be carried out in the presence of a polymerization initiator. The polymerization initiator is not particularly limited as long as it can generate radicals within the above-mentioned polymerization temperature range, and known oil-soluble and / or water-soluble polymerization initiators can be used. Furthermore, the polymerization can be initiated as a redox reaction by combining with a reducing agent or the like. The concentration of the polymerization initiator is determined appropriately depending on the type of monomer, the molecular weight of the target polymer, and the reaction rate.

[0261] As the polymerization initiator, persulfates (e.g., ammonium persulfate), or organic peroxides such as disuccinic acid peroxide and diglutaric acid peroxide can be used alone or in the form of a mixture thereof. They may also be used in combination with a reducing agent such as sodium sulfite to form a redox system. Furthermore, during polymerization, a radical scavenger such as hydroquinone or catechol, or a peroxide decomposer such as ammonium sulfite, can be added to adjust the radical concentration in the system.

[0262] As the polymerization initiator, persulfates are particularly preferred because they can easily produce polymers with higher molecular weights. Examples of persulfates include ammonium persulfate, potassium persulfate, and sodium persulfate, with ammonium persulfate being preferred.

[0263] The amount of polymerization initiator to be added is not particularly limited, but may be added all at once, stepwise, or continuously at the beginning of polymerization in an amount (for example, several ppm relative to the water concentration) that does not significantly decrease the polymerization rate. The upper limit is a range in which the reaction temperature can be increased while removing heat from the equipment using the heat of polymerization reaction, and a more preferred upper limit is a range in which the heat of polymerization reaction can be removed from the equipment.

[0264] In the production methods (11) to (13), the polymerization initiator can be added not only at the start of polymerization but also during polymerization. The ratio of the amount of polymerization initiator added at the start of polymerization to the amount of polymerization initiator added during polymerization is preferably 95 / 5 to 5 / 95, more preferably 60 / 40 to 10 / 90, and even more preferably 30 / 70 to 15 / 85. The method of adding the polymerization initiator during polymerization is not particularly limited, and the entire amount may be added at once, or may be added in two or more divided portions, or may be added continuously.

[0265] In the production methods (11) to (13), since polymers with higher molecular weights can be easily produced, the total amount of polymerization initiators used in the polymerization is preferably 0.00001 to 10% by mass relative to the aqueous medium. The total amount of polymerization initiators used in the polymerization is more preferably 0.0001% by mass or more, even more preferably 0.001% by mass or more, particularly preferably 0.01% by mass or more, more preferably 5% by mass or less, and even more preferably 2% by mass or less.

[0266] In the production methods (11) to (13), since polymers with higher molecular weights can be easily produced, the total amount of polymerization initiators used in the polymerization is preferably 0.001 to 10 mol% based on the monomers. The total amount of polymerization initiators used in the polymerization is more preferably 0.005 mol% or more, even more preferably 0.01 mol% or more, particularly preferably 0.1 mol% or more, most preferably 0.5 mol% or more, more preferably 5 mol% or less, even more preferably 2.5 mol% or less, particularly preferably 2.2 mol% or less, and most preferably 2.0 mol% or less.

[0267] In the production methods (11) to (13), since polymers with higher molecular weights can be easily produced, the amount of monomers containing monomers (11) to (13) present at the start of polymerization is preferably 20% by mass or more relative to the amount of aqueous medium present. The amount of monomer present is more preferably 30% by mass or more, and even more preferably 40% by mass or more. There are no particular restrictions on the upper limit of the amount of monomer present, but from the viewpoint of smoothly progressing polymerization, it may be 200% by mass or less. The amount of monomer present at the start of polymerization refers to the total amount of monomers (11) to (13) and, if present, other monomers present in the reactor at the start of polymerization.

[0268] In the production methods (11) to (13), the polymerization may be carried out in the presence of a pH adjuster, which may be added before or after the start of the polymerization.

[0269] Examples of pH adjusters that can be used include ammonia, sodium hydroxide, potassium hydroxide, sodium carbonate, potassium carbonate, ammonium carbonate, sodium bicarbonate, potassium bicarbonate, ammonium bicarbonate, sodium phosphate, potassium phosphate, sodium citrate, potassium citrate, ammonium citrate, sodium gluconate, potassium gluconate, and ammonium gluconate.

[0270] In the production methods (11) to (13), the polymerization of the monomers (11) to (13) can be carried out by charging a reactor with an aqueous medium, any of the monomers (11) to (13), and, if necessary, other monomers and, if necessary, other additives, stirring the contents of the reactor, maintaining the reactor at a predetermined polymerization temperature, and then adding a predetermined amount of polymerization initiator to initiate the polymerization reaction. After the initiation of the polymerization reaction, the monomer, polymerization initiator, and other additives may be added depending on the purpose.

[0271] In the production methods (11) to (13), the polymerization of the monomers can be carried out substantially in the absence of a fluorinated surfactant. In the present disclosure, "substantially in the absence of a fluorinated surfactant" means that the amount of the fluorinated surfactant relative to the aqueous medium is 10 ppm by mass or less. The amount of the fluorinated surfactant relative to the aqueous medium is preferably 1 ppm by mass or less, more preferably 100 ppb by mass or less, even more preferably 10 ppb by mass or less, and even more preferably 1 ppb by mass or less.

[0272] The fluorine-containing surfactant will be described later in the explanation regarding the polymerization of fluoromonomers.

[0273] (composition) The composition to be subjected to the fluorine radical treatment can be produced, for example, by polymerizing a fluoromonomer in the presence of polymer (I). By such a production method, a composition containing a fluoropolymer (excluding polymer (I)) and polymer (I) is obtained.

[0274] The composition to be subjected to the fluorine radical treatment can be produced by polymerizing a fluoromonomer in an aqueous medium in the presence of the polymer (I). By such a production method, an aqueous dispersion containing the fluoropolymer (excluding the polymer (I)), the polymer (I), and the aqueous medium is obtained as the composition.

[0275] The fluoromonomer preferably has at least one double bond. Examples of the fluoromonomer include tetrafluoroethylene (TFE), hexafluoropropylene (HFP), chlorotrifluoroethylene (CTFE), vinyl fluoride, vinylidene fluoride (VDF), trifluoroethylene, fluoroalkyl vinyl ether, fluoroalkyl ethylene, fluoroalkyl allyl ether, trifluoropropylene, pentafluoropropylene, trifluorobutene, tetrafluoroisobutene, hexafluoroisobutene, and fluoroalkyl ethers represented by the general formula (100): CHX 101 =CX 102 Rf 101 (In the formula, X 101 and X 102 is H on one side and F on the other side, and Rf 101 is preferably at least one selected from the group consisting of a fluoromonomer represented by (wherein is a linear or branched fluoroalkyl group having 1 to 12 carbon atoms) and a fluorinated vinyl heterocyclic compound.

[0276] Examples of the fluoroalkyl vinyl ether include: General formula (110): CF2=CF-ORf 111 (In the formula, Rf 111 represents a perfluoroorganic group; General formula (120): CF2=CF-OCH2-Rf 121 (In the formula, Rf 121 is a perfluoroalkyl group having 1 to 5 carbon atoms), General formula (130): CF2=CFOCF2ORf 131 (In the formula, Rf 131 is a linear or branched perfluoroalkyl group having 1 to 6 carbon atoms, a cyclic perfluoroalkyl group having 5 to 6 carbon atoms, or a linear or branched perfluorooxyalkyl group having 2 to 6 carbon atoms and containing 1 to 3 oxygen atoms, General formula (140): CF2=CFO(CF2CF(Y 141 )O) m(CF2) n F (In the formula, Y 141 represents a fluorine atom or a trifluoromethyl group, m is an integer of 1 to 4, and n is an integer of 1 to 4. General formula (150): CF2=CF-O-(CF2CFY 151 -O) n -(CFY 152 ) m -A 151 (In the formula, Y 151 represents a fluorine atom, a chlorine atom, a -SO2F group, or a perfluoroalkyl group. The perfluoroalkyl group may contain an etheric oxygen and a -SO2F group. n represents an integer of 0 to 3. n Y 151 may be the same or different. 152 represents a fluorine atom, a chlorine atom, or a -SO2F group. m represents an integer of 1 to 5. m Y 152 may be the same or different. 151 -SO2X 151 , -COZ 151 or -POZ 152 Z 153 represents X 151 are F, Cl, Br, I, -OR 151 or -NR 152 R 153 represents Z. 151 , Z 152 and Z 153 are the same or different and are -NR 154 R 155 -OR 156 Represents R 151 , R 152 , R 153 , R 154 , R 155 and R 156 are the same or different and represent H, ammonium, an alkali metal, an alkyl group which may contain a fluorine atom, an aryl group, or a sulfonyl-containing group. It is preferable that the material is at least one selected from the group consisting of:

[0277] In the present disclosure, the term "perfluoroorganic group" refers to an organic group in which all hydrogen atoms bonded to carbon atoms are substituted with fluorine atoms. The perfluoroorganic group may have an ether oxygen atom.

[0278] The fluoromonomer represented by the general formula (110) is Rf 111 is a perfluoroalkyl group having 1 to 10 carbon atoms. The number of carbon atoms in the perfluoroalkyl group is preferably 1 to 5.

[0279] Examples of the perfluoroorganic group in the general formula (110) include a perfluoromethyl group, a perfluoroethyl group, a perfluoropropyl group, a perfluorobutyl group, a perfluoropentyl group, and a perfluorohexyl group. The fluoromonomer represented by the general formula (110) further includes a fluoromonomer represented by the general formula (110) in which Rf 111 is a perfluoro(alkoxyalkyl) group having 4 to 9 carbon atoms, Rf 111 is the following formula:

[0280] [ka]

[0281] (wherein m represents 0 or an integer of 1 to 4), and Rf is a group represented by the following formula:

[0282] CF3CF2CF2-(O-CF(CF3)-CF2) n - (wherein n represents an integer of 1 to 4).

[0283] Among the fluoromonomers represented by the general formula (110), General formula (160): CF2=CF-ORf 161 (In the formula, Rf 161Rf represents a perfluoroalkyl group having 1 to 10 carbon atoms. Fluoromonomers represented by 161 is preferably a perfluoroalkyl group having 1 to 5 carbon atoms.

[0284] The fluoroalkyl vinyl ether is preferably at least one selected from the group consisting of fluoromonomers represented by the general formulas (160), (130) and (140).

[0285] The fluoromonomer represented by general formula (160) is preferably at least one selected from the group consisting of perfluoro(methyl vinyl ether), perfluoro(ethyl vinyl ether), and perfluoro(propyl vinyl ether), and more preferably at least one selected from the group consisting of perfluoro(methyl vinyl ether) and perfluoro(propyl vinyl ether).

[0286] The fluoromonomer represented by the general formula (130) is preferably at least one selected from the group consisting of CF2=CFOCF2OCF3, CF2=CFOCF2OCF2CF3, and CF2=CFOCF2OCF2CF2OCF3.

[0287] The fluoromonomer represented by general formula (140) is preferably at least one selected from the group consisting of CF2=CFOCF2CF(CF3)O(CF2)3F, CF2=CFO(CF2CF(CF3)O)2(CF2)3F, and CF2=CFO(CF2CF(CF3)O)2(CF2)2F.

[0288] The fluoromonomer represented by general formula (150) is preferably at least one selected from the group consisting of CF2=CFOCF2CF2SO2F, CF2=CFOCF2CF(CF3)OCF2CF2SO2F, CF2=CFOCF2CF(CF2CF2SO2F)OCF2CF2SO2F and CF2=CFOCF2CF(SO2F)2.

[0289] The fluoromonomer represented by the general formula (100) is Rf 101 is a linear fluoroalkyl group, and Rf 101 More preferred is a fluoromonomer in which Rf is a linear perfluoroalkyl group. 101 The number of carbon atoms in the formula (100) is preferably 1 to 6. Examples of the fluoromonomer represented by the formula (100) include CH2=CFCF3, CH2=CFCF2CF3, CH2=CFCF2CF2CF3, CH2=CFCF2CF2CF2H, CH2=CFCF2CF2CF2CF3, CHF=CHCF3 (E-isomer), and CHF=CHCF3 (Z-isomer), and among these, 2,3,3,3-tetrafluoropropylene represented by CH2=CFCF3 is preferred.

[0290] Fluoroalkylethylenes include: General formula (170): CH2=CH-(CF2) n -X 171 (In the formula, X 171 is H or F, and n is an integer of 3 to 10.) is preferred, and fluoroalkylethylenes represented by CH2=CH-C4F9 and CH2=CH-C6F 13 It is more preferable that the material is at least one selected from the group consisting of:

[0291] Examples of the fluoroalkyl allyl ether include: General formula (180): CF2=CF-CF2-ORf 111 (In the formula, Rf 111 represents a perfluoroorganic group.

[0292] Rf of general formula (180) 111 is Rf in general formula (110) 111 is the same as Rf 111is preferably a perfluoroalkyl group having 1 to 10 carbon atoms or a perfluoroalkoxyalkyl group having 1 to 10 carbon atoms. The fluoroalkyl allyl ether represented by general formula (180) is preferably at least one selected from the group consisting of CF2=CF-CF2-O-CF3, CF2=CF-CF2-O-C2F5, CF2=CF-CF2-O-C3F7, and CF2=CF-CF2-O-C4F9, more preferably at least one selected from the group consisting of CF2=CF-CF2-O-C2F5, CF2=CF-CF2-O-C3F7, and CF2=CF-CF2-O-C4F9, and even more preferably CF2=CF-CF2-O-CF2CF2CF3.

[0293] The fluorinated vinyl heterocycle includes a compound represented by the general formula (230): [ka] (In the formula, X 231 and X 232 are independently F, Cl, a methoxy group, or a fluorinated methoxy group; Y 231 is the formula Y 232 or formula Y 233 is.

[0294] [ka] (In the formula, Z 231 and Z 232 are independently F or a fluorinated alkyl group having 1 to 3 carbon atoms.

[0295] In the polymerization, the fluoromonomer and a non-fluorine-containing monomer may be polymerized. Examples of the non-fluorine-containing monomer include hydrocarbon-based monomers reactive with the fluoromonomer. Examples of the hydrocarbon-based monomer include alkenes such as ethylene, propylene, butylene, and isobutylene; alkyl vinyl ethers such as ethyl vinyl ether, propyl vinyl ether, butyl vinyl ether, isobutyl vinyl ether, and cyclohexyl vinyl ether; vinyl acetate, vinyl propionate, vinyl n-butyrate, vinyl isobutyrate, vinyl valerate, vinyl pivalate, vinyl caproate, vinyl caprylate, vinyl caprate, vinyl versatate, vinyl laurate, vinyl myristate, vinyl palmitate, vinyl stearate, vinyl benzoate, vinyl para-t-butylbenzoate, vinyl cyclohexanecarboxylate, vinyl monochloroacetate, vinyl adipate, vinyl acrylate, vinyl methacrylate, vinyl crotonate, vinyl sorbate, vinyl cinnamate, vinyl undecylenate, vinyl hydroxyacetate, and vinyl hydroxybenzoates. vinyl esters such as vinyl hydroxypropionate, vinyl hydroxybutyrate, vinyl hydroxyvalerate, vinyl hydroxyisobutyrate, and vinyl hydroxycyclohexanecarboxylate; alkyl allyl ethers such as ethyl allyl ether, propyl allyl ether, butyl allyl ether, isobutyl allyl ether, and cyclohexyl allyl ether; alkyl allyl esters such as ethyl allyl ester, propyl allyl ester, butyl allyl ester, isobutyl allyl ester, and cyclohexyl allyl ester; and (meth)acrylic acid esters such as methyl acrylate, methyl methacrylate, ethyl acrylate, ethyl methacrylate, propyl acrylate, propyl methacrylate, butyl acrylate, butyl methacrylate, hexyl methacrylate, cyclohexyl methacrylate, and vinyl methacrylate.

[0296] The above-mentioned fluorine-free monomer may also be a functional group-containing hydrocarbon monomer. Examples of the above-mentioned functional group-containing hydrocarbon monomer include hydroxyalkyl vinyl ethers such as hydroxyethyl vinyl ether, hydroxypropyl vinyl ether, hydroxybutyl vinyl ether, hydroxyisobutyl vinyl ether, and hydroxycyclohexyl vinyl ether; fluorine-free monomers having a carboxyl group such as acrylic acid, methacrylic acid, itaconic acid, succinic acid, succinic anhydride, fumaric acid, fumaric anhydride, crotonic acid, maleic acid, maleic anhydride, and perfluorobutenoic acid; fluorine-free monomers having a sulfo group such as vinyl sulfonic acid; fluorine-free monomers having a glycidyl group such as glycidyl vinyl ether and glycidyl allyl ether; fluorine-free monomers having an amino group such as aminoalkyl vinyl ether and aminoalkyl allyl ether; fluorine-free monomers having an amide group such as (meth)acrylamide and methylolacrylamide; and fluorine-free monomers having a nitrile group such as acrylonitrile and methacrylonitrile.

[0297] In the above polymerization, desired fluoropolymer particles can be obtained by polymerizing one or more of the above fluoromonomers. For example, tetrafluoroethylene and a modified monomer can be polymerized as the fluoromonomer. Alternatively, tetrafluoroethylene and at least one selected from the group consisting of hexafluoropropylene, perfluoro(alkyl vinyl ether), and perfluoroallyl ether can be polymerized as the fluoromonomer.

[0298] The amount of polymer (I) added in the polymerization is preferably 0.0001 to 10% by mass relative to the aqueous medium, with a more preferred lower limit of 0.001% by mass or more and a more preferred upper limit of 1% by mass or less. By setting the amount of polymer (I) added within the above range, the polymerization of the fluoromonomer in the aqueous medium can proceed smoothly. The amount of polymer (I) added is the total amount of polymer (I) added in the polymerization.

[0299] In the polymerization, the polymer (I) may be added all at once, or may be added continuously. Continuous addition of the polymer (I) means, for example, adding the polymer (I) over time, without interruption, or in portions, rather than all at once. In the polymerization, an aqueous solution containing the polymer (I) and water may be prepared, and the aqueous solution may be added.

[0300] In the above polymerization, it is preferable to start adding polymer (I) before the solid content of the fluoropolymer formed in the aqueous medium reaches 0.5 mass%, and to continue adding polymer (I) continuously thereafter. The timing to start adding polymer (I) is preferably before the solid content of the fluoropolymer reaches 0.3 mass%, more preferably before it reaches 0.2 mass%, even more preferably before it reaches 0.1 mass%, and particularly preferably at the same time as the start of polymerization. The above solid content is the content of the fluoropolymer relative to the total of the aqueous medium and the fluoropolymer.

[0301] In the above polymerization, the use of at least one polymer (I) allows efficient production of a fluoropolymer. Two or more compounds included in the polymer (I) may be used simultaneously, and other surfactant compounds other than the polymer (I) may be used simultaneously, as long as they are volatile or may remain in a molded product made of the fluoropolymer.

[0302] A nucleating agent may be used in the polymerization. The amount of the nucleating agent added can be appropriately selected depending on the type of nucleating agent. The amount of the nucleating agent added may be 5000 ppm by mass or less, preferably 1000 ppm by mass or less, more preferably 500 ppm by mass or less, even more preferably 100 ppm by mass or less, particularly preferably 50 ppm by mass or less, and most preferably 10 ppm by mass or less, relative to the aqueous medium.

[0303] In the above polymerization, it is preferable to add a nucleating agent to the aqueous medium before the start of polymerization or before the solid content of the fluoropolymer formed in the aqueous medium reaches 5.0 mass %. By adding the nucleating agent at the early stage of polymerization, an aqueous dispersion having a small average primary particle size and excellent stability can be obtained.

[0304] The amount of the nucleating agent added at the beginning of polymerization is preferably 0.001% by mass or more, more preferably 0.01% by mass or more, still more preferably 0.05% by mass or more, and particularly preferably 0.1% by mass or more, based on the fluoropolymer to be obtained. The upper limit of the amount of the nucleating agent added at the beginning of polymerization is not limited, but is, for example, 2000% by mass.

[0305] The use of a nucleating agent results in a fluoropolymer having a smaller primary particle size compared to polymerization carried out in the absence of said nucleating agent.

[0306] Examples of the nucleating agent include dicarboxylic acids, perfluoropolyether (PFPE) acids or salts thereof, hydrocarbon-containing surfactants, etc. The nucleating agent preferably does not contain an aromatic ring and is preferably an aliphatic compound.

[0307] The nucleating agent is preferably added before or simultaneously with the addition of the polymerization initiator, but the particle size distribution can also be adjusted by adding it during the polymerization.

[0308] The amount of the dicarboxylic acid is preferably 1000 ppm by mass or less, more preferably 500 ppm by mass or less, and even more preferably 100 ppm by mass or less, relative to the aqueous medium.

[0309] The perfluoropolyether (PFPE) acid or salt thereof may have any chain structure in which oxygen atoms in the main chain of the molecule are separated by saturated fluorocarbon groups having 1 to 3 carbon atoms. Two or more types of fluorocarbon groups may be present in the molecule. A typical structure has a repeating unit represented by the following formula: (-CFCF3-CF2-O-) n (VII) (-CF2-CF2-CF2-O-) n (VIII) (-CF2-CF2-O-) n -(-CF2-O-) m (IX) (-CF2-CFCF3-O-)n-(-CF2-O-) m (X)

[0310] These structures are described by Kasai in J. Appl. Polymer Sci. 57, 797 (1995). As disclosed therein, the PFPE acid or its salt may have a carboxylic acid group or its salt at one or both ends. The PFPE acid or its salt may also have a sulfonic acid or phosphonic acid group or their salt at one or both ends. The PFPE acid or its salt may also have a different group at each end. For monofunctional PFPEs, the other end of the molecule is usually perfluorinated but may contain a hydrogen or chlorine atom. The PFPE acid or its salt has at least two ether oxygens, preferably at least four ether oxygens, and even more preferably at least six ether oxygens. Preferably, at least one of the fluorocarbon groups separating the ether oxygens, and more preferably at least two of such fluorocarbon groups, has two or three carbon atoms. Even more preferably, at least 50% of the fluorocarbon groups separating the ether oxygens have two or three carbon atoms. Also, preferably, the PFPE acid or salt thereof has a total of at least 15 carbon atoms, for example, the preferred minimum value of n or n+m in the repeating unit structure is at least 5. Two or more of the PFPE acids or salts thereof having acid groups at one or both ends can be used in the manufacturing method of the present disclosure. The PFPE acid or salt thereof preferably has a number average molecular weight of less than 6000 g / mol.

[0311] The amount of the hydrocarbon-containing surfactant added is preferably 40 ppm by mass or less, more preferably 30 ppm by mass or less, and even more preferably 20 ppm by mass or less, relative to the aqueous medium. It is estimated that the ppm amount of lipophilic nucleation sites present in the aqueous medium is less than the amount added. Therefore, the amount of lipophilic nucleation sites is less than the 40 ppm by mass, 30 ppm by mass, and 20 ppm by mass, respectively. Since the lipophilic nucleation sites are thought to exist as molecules, even a small amount of the hydrocarbon-containing surfactant can generate a large amount of lipophilic nucleation sites. Therefore, beneficial effects can be obtained by adding only about 1 ppm by mass of the hydrocarbon-containing surfactant to the aqueous medium. A preferred lower limit is 0.01 ppm by mass, and a more preferred lower limit is 0.1 ppm by mass.

[0312] The hydrocarbon-containing surfactants include nonionic and cationic surfactants, including siloxane surfactants such as those disclosed in U.S. Pat. No. 7,897,682 (Brothers et al.) and U.S. Pat. No. 7,977,438 (Brothers et al.).

[0313] The hydrocarbon-containing surfactant is preferably a nonionic surfactant (e.g., a nonionic hydrocarbon surfactant). That is, the nucleating agent is preferably a nonionic surfactant. The nonionic surfactant preferably does not contain an aromatic moiety.

[0314] Examples of the nonionic surfactant include those represented by the following general formula (i): R 3 -OA 1 -H(i) (In the formula, R 3 is a linear or branched primary or secondary alkyl group having 8 to 18 carbon atoms, and A 1 is a polyoxyalkylene chain. R 3 The number of carbon atoms in R is preferably 10 to 16, and more preferably 12 to 16. 3When the carbon number of R is 18 or less, good dispersion stability of the aqueous dispersion is easily obtained. 3 If the carbon number exceeds 18, the flow temperature is high and it is difficult to handle. 3 If the number of carbon atoms is less than 8, the surface tension of the aqueous dispersion increases, and the permeability and wettability tend to decrease.

[0315] A 1 The polyoxyalkylene chain may be composed of oxyethylene and oxypropylene. The polyoxyalkylene chain has an average repeat number of 5 to 20 oxyethylene groups and an average repeat number of 0 to 2 oxypropylene groups, and is a hydrophilic group. The number of oxyethylene units may include either a broad or narrow unimodal distribution, which is typically provided, or a broader or bimodal distribution obtained by blending. When the average repeat number of oxypropylene groups is greater than 0, the oxyethylene groups and oxypropylene groups in the polyoxyalkylene chain may be arranged in a block or random configuration. From the viewpoint of viscosity and stability of the aqueous dispersion, a polyoxyalkylene chain having an average repeat number of 7 to 12 oxyethylene groups and an average repeat number of 0 to 2 oxypropylene groups is preferred. 1 If the oxypropylene group has an average of 0.5 to 1.5, low foaming properties are favorable and it is preferable.

[0316] More preferably, R 3 is (R')(R")HC-, where R' and R" are the same or different straight, branched, or cyclic alkyl groups having a total of at least 5, preferably 7 to 17, carbon atoms. Preferably, at least one of R' or R" is a branched or cyclic hydrocarbon group.

[0317] Specific examples of nonionic surfactants include C 13 H 27 -O-(C2H4O) n -H, C 12 H 25 -O-(C2H4O) n -H, C 10 H21 CH(CH3)CH2-O-(C2H4O) n -H, C 13 H 27 -O-(C2H4O) n -(CH(CH3)CH2O)-H, C 16 H 33 -O-(C2H4O) n -H, HC(CH 11 )(C7H 15 )-O-(C2H4O) n -H (wherein n is an integer of 1 or more), and the like.

[0318] For example, the nonionic surfactant may be a polyethylene glycol-polypropylene glycol-polyethylene glycol block copolymer.

[0319] Commercially available nonionic surfactants include, for example, the Genapol X series (manufactured by Clariant) such as Genapol X080 (trade name), the Noigen TDS series (manufactured by Dai-ichi Kogyo Seiyaku Co., Ltd.) such as Noigen TDS-80 (trade name), the Leocol TD series (manufactured by Lion Chemical) such as Leocol TD-90 (trade name), the Lionol (registered trademark) TD series (manufactured by Lion Chemical), the T-Det A series (manufactured by Harcros Chemicals) such as T-Det A138 (trade name), and the Tergitol (registered trademark) 15S series (manufactured by The Dow Chemical Company).

[0320] The nonionic surfactant is preferably an ethoxylate of 2,6,8-trimethyl-4-nonanol having an average of about 4 to about 18 ethylene oxide units, an ethoxylate of 2,6,8-trimethyl-4-nonanol having an average of about 6 to about 12 ethylene oxide units, or a mixture thereof. Nonionic surfactants of this type are also commercially available, for example, under the trade names TERGITOL TMN-6, TERGITOL TMN-10, and TERGITOL TMN-100X (all trade names, manufactured by The Dow Chemical Company).

[0321] The hydrophobic group of the nonionic surfactant may be any of an alkylphenol group, a linear alkyl group, and a branched alkyl group. For example, the polyoxyethylene alkylphenyl ether-based nonionic compound may be, for example, a compound represented by the following general formula (ii): R 4 -C6H4-OA 2 -H (ii) (In the formula, R 4 is a linear or branched alkyl group having 4 to 12 carbon atoms, and A 2 is a polyoxyalkylene chain.) Specific examples of the polyoxyethylene alkylphenyl ether-based nonionic compounds include Triton X-100 (trade name, manufactured by Dow Chemical Company).

[0322] A 2 The polyoxyalkylene chain may be composed of oxyethylene and oxypropylene. It is a polyoxyalkylene chain having an average repeat number of 5 to 20 oxyethylene groups and an average repeat number of 0 to 2 oxypropylene groups, and is a hydrophilic group. The number of oxyethylene units may include either a broad or narrow unimodal distribution as is usually provided, or a broader or bimodal distribution obtained by blending. When the average repeat number of oxypropylene groups is more than 0, the oxyethylene groups and oxypropylene groups in the polyoxyalkylene chain may be arranged in a block or random configuration. From the viewpoint of the viscosity and sedimentation stability of the composition, a polyoxyalkylene chain having an average repeat number of 7 to 12 oxyethylene groups and an average repeat number of 0 to 2 oxypropylene groups is preferred. In particular, A 2 If the oxypropylene group has an average of 0.5 to 1.5, low foaming properties are favorable and it is preferable.

[0323] More preferably, R 7is a primary or secondary alkyl group, more preferably (R')(R")HC-, where R' and R" are the same or different straight-chain, branched-chain, or cyclic alkyl groups having a total of at least 5, preferably 7 to 17 carbon atoms. Preferably, at least one of R' or R" is a branched-chain or cyclic hydrocarbon group.

[0324] The nonionic surfactant also includes a polyol compound, specifically, those described in WO 2011 / 014715. Typical examples of polyol compounds include compounds having one or more sugar units as polyol units. The sugar units may be modified to contain at least one long chain. Suitable polyol compounds containing at least one long chain moiety include, for example, alkyl glycosides, modified alkyl glycosides, sugar esters, and combinations thereof. Sugars include, but are not limited to, monosaccharides, oligosaccharides, and sorbitan. Monosaccharides include pentoses and hexoses. Typical examples of monosaccharides include ribose, glucose, galactose, mannose, fructose, arabinose, and xylose. Oligosaccharides include oligomers of 2 to 10 identical or different monosaccharides. Examples of oligosaccharides include, but are not limited to, sucrose, maltose, lactose, raffinose, and isomaltose.

[0325] Typically, sugars suitable for use as polyol compounds include cyclic compounds containing a five-membered ring with four carbon atoms and one heteroatom (typically oxygen or sulfur, but preferably an oxygen atom), or a six-membered ring with five carbon atoms and one heteroatom, preferably an oxygen atom, as described above. These further contain at least two or at least three hydroxy groups (-OH groups) attached to the carbon ring atoms. Typically, the sugars are modified in that one or more of the hydrogen atoms of the hydroxy groups (and / or hydroxyalkyl groups) attached to the carbon ring atoms are replaced by a long-chain residue, such that an ether or ester bond is created between the long-chain residue and the sugar moiety. The sugar-based polyol may contain one or more sugar units. The sugar unit or units may be modified with long chain moieties as described above. Specific examples of sugar-based polyol compounds include glycosides, sugar esters, sorbitan esters, and mixtures and combinations thereof.

[0326] A preferred class of polyol compounds are the alkyl or modified alkyl glucosides. These classes of surfactants contain at least one glucose moiety. [ka] (wherein x represents 0, 1, 2, 3, 4, or 5; R 1 and R 2 independently represent H or a long chain unit containing at least 6 carbon atoms, with the proviso that R 1 and R 2 and at least one of R is not H. 1 and R 2Typical examples of the fatty alcohol include hexanol, heptanol, octanol, nonanol, decanol, undecanol, dodecanol (lauryl alcohol), tetradecanol, hexadecanol (cetyl alcohol), heptadecanol, octadecanol (stearyl alcohol), eicosanoic acid, and combinations thereof. While the above formula represents a specific example of an alkyl polyglucoside showing glucose in the pyranose form, it is understood that other sugars or sugars that are the same sugar but in different enantiomeric or diastereomeric forms may also be used. Alkyl glucosides can be obtained, for example, by the acid-catalyzed reaction of glucose, starch, or n-butyl glucoside with aliphatic alcohols, typically resulting in a mixture of various alkyl glucosides (Alkylpolygylcoside, Rompp, Lexikon Chemie, Version 2.0, Stuttgart / New York, Georg Thieme Verlag, 1999). Examples of aliphatic alcohols include hexanol, heptanol, octanol, nonanol, decanol, undecanol, dodecanol (lauryl alcohol), tetradecanol, hexadecanol (cetyl alcohol), heptadecanol, octadecanol (stearyl alcohol), eicosanoic acid, and combinations thereof. Alkyl glucosides are also commercially available from Cognis GmbH, Dusseldorf, Germany, under the trade names GLUCOPON or DISPONIL.

[0327] Other nonionic surfactants include difunctional block copolymers supplied by BASF as part of the Pluronic® R series, and tridecyl alcohol alkoxylates supplied by BASF as part of the Iconol® TDA series.

[0328] In the polymerization, a compound having a functional group capable of reacting by radical polymerization and a hydrophilic group may be used together with the polymer (I). The compound having a functional group capable of reacting by radical polymerization and a hydrophilic group may be the same compound as the modifying monomer (A) described below.

[0329] In the polymerization, in addition to the polymer (I) and, if desired, other surfactant compounds, additives for stabilizing each compound may be used, such as buffers, pH adjusters, stabilizing aids, and dispersion stabilizers.

[0330] The stabilizing aid is preferably paraffin wax, fluorine-based oil, fluorine-based solvent, silicone oil, etc. The stabilizing aid may be used alone or in combination of two or more. The stabilizing aid is more preferably paraffin wax. The paraffin wax may be liquid, semi-solid, or solid at room temperature, but is preferably a saturated hydrocarbon having 12 or more carbon atoms. The melting point of the paraffin wax is usually preferably 40 to 65°C, more preferably 50 to 65°C.

[0331] The amount of the stabilizing aid used is preferably 0.1 to 12 mass % based on the mass of the aqueous medium used, and more preferably 0.1 to 8 mass %. It is desirable that the stabilizing aid is sufficiently hydrophobic so that it is completely separated from the aqueous dispersion after polymerization and does not become a contaminating component.

[0332] The polymerization is carried out by charging an aqueous medium, the polymer (I), a monomer, and other additives as necessary into a polymerization reactor, stirring the contents of the reactor, maintaining the reactor at a predetermined polymerization temperature, and then adding a predetermined amount of a polymerization initiator to initiate the polymerization reaction. After the polymerization reaction has started, additional monomers, polymerization initiators, chain transfer agents, polymer (I), etc. may be added depending on the purpose. Polymer (I) may also be added after the polymerization reaction has started.

[0333] Usually, the polymerization temperature is 5 to 120° C. and the polymerization pressure is 0.05 to 10 MPaG. The polymerization temperature and polymerization pressure are appropriately determined depending on the type of monomer used, the molecular weight of the desired fluoropolymer, and the reaction rate.

[0334] The polymerization initiator is not particularly limited as long as it can generate radicals within the polymerization temperature range, and known oil-soluble and / or water-soluble polymerization initiators can be used. Furthermore, polymerization can also be initiated as a redox reaction in combination with a reducing agent, etc. The concentration of the polymerization initiator is determined appropriately depending on the type of monomer, the molecular weight of the desired fluoropolymer, and the reaction rate.

[0335] As the polymerization initiator, an oil-soluble radical polymerization initiator or a water-soluble radical polymerization initiator can be used.

[0336] The oil-soluble radical polymerization initiator may be a known oil-soluble peroxide, for example, dialkyl peroxycarbonates such as diisopropyl peroxydicarbonate and di-sec-butyl peroxydicarbonate, peroxyesters such as t-butyl peroxyisobutyrate and t-butyl peroxypivalate, dialkyl peroxides such as di-t-butyl peroxide, and also di(ω-hydro-dodecafluoroheptanoyl) peroxide, di(ω-hydro-tetradecafluorooctanoyl) peroxide, di(ω-hydro-hexadecafluorononanoyl) peroxide, di(perfluorobutyryl) peroxide, di(perfluorovaleryl) peroxide, di(perfluorohexanoyl) peroxide, di(perfluoroheptanoyl) peroxide, di(perfluorooctanoyl) peroxide, di(perfluorononanoyl) peroxide, di(ω-chloro Representative examples include di[perfluoro(or fluorochloro)acyl]peroxides such as di(ω-hexafluorobutyryl)peroxide, di(ω-chloro-decafluorohexanoyl)peroxide, di(ω-chloro-tetradecafluorooctanoyl)peroxide, ω-hydro-dodecafluoroheptanoyl-ω-hydrohexadecafluorononanoyl-peroxide, ω-chloro-hexafluorobutyryl-ω-chloro-decafluorohexanoyl-peroxide, ω-hydrododecafluoroheptanoyl-perfluorobutyryl-peroxide, di(dichloropentafluorobutanoyl)peroxide, di(trichlorooctafluorohexanoyl)peroxide, di(tetrachloroundecafluorooctanoyl)peroxide, di(pentachlorotetradecafluorodecanoyl)peroxide, and di(undecachlorodotriacontafluorodocosanoyl)peroxide.

[0337] The water-soluble radical polymerization initiator may be a known water-soluble peroxide, such as ammonium salts, potassium salts, or sodium salts of persulfuric acid, perborate, perchloric acid, perphosphoric acid, or percarbonate; organic peroxides such as disuccinic acid peroxide or diglutaric acid peroxide; t-butyl permaleate; or t-butyl hydroperoxide. A reducing agent such as sulfites or sulfites may also be contained, and the amount used may be 0.1 to 20 times the amount of the peroxide.

[0338] For example, when polymerization is carried out at low temperatures below 30°C, it is preferable to use a redox initiator, which combines an oxidizing agent and a reducing agent, as the polymerization initiator. Examples of oxidizing agents include persulfates, organic peroxides, potassium permanganate, manganese triacetate, and cerium ammonium nitrate. Examples of reducing agents include sulfites, bisulfites, bromates, diimines, and oxalic acid. Examples of persulfates include ammonium persulfate and potassium persulfate. Examples of sulfites include sodium sulfite and ammonium sulfite. To increase the decomposition rate of the initiator, it is also preferable to add a copper salt or an iron salt to the redox initiator combination. Examples of copper salts include copper(II) sulfate, and examples of iron salts include iron(II) sulfate.

[0339] Examples of the redox initiator include potassium permanganate / oxalic acid, ammonium persulfate / bisulfite / iron sulfate, manganese triacetate / oxalic acid, cerium ammonium nitrate / oxalic acid, and bromate / bisulfite, with potassium permanganate / oxalic acid being preferred. When using a redox initiator, either an oxidizing agent or a reducing agent may be charged into a polymerization vessel in advance, and then the other may be added continuously or intermittently to initiate polymerization. For example, when potassium permanganate / oxalic acid is used, it is preferred to charge oxalic acid into a polymerization vessel and then continuously add potassium permanganate thereto.

[0340] The amount of polymerization initiator to be added is not particularly limited, but may be added all at once, stepwise, or continuously at the beginning of polymerization in an amount (for example, several ppm relative to the water concentration) that does not significantly decrease the polymerization rate. The upper limit is a range in which the reaction temperature can be increased while removing heat from the equipment using the heat of polymerization reaction, and a more preferred upper limit is a range in which the heat of polymerization reaction can be removed from the equipment.

[0341] The aqueous medium is a reaction medium for polymerization and refers to a liquid containing water. The aqueous medium is not particularly limited as long as it contains water, and may contain water and, for example, a fluorine-free organic solvent such as an alcohol, ether, or ketone, and / or a fluorine-containing organic solvent having a boiling point of 40° C. or lower.

[0342] In the above polymerization, known chain transfer agents, radical scavengers and decomposers may be added depending on the purpose to adjust the polymerization rate and molecular weight.

[0343] Examples of the chain transfer agent include esters such as dimethyl malonate, diethyl malonate, methyl acetate, ethyl acetate, butyl acetate, and dimethyl succinate, as well as isopentane, methane, ethane, propane, methanol, isopropanol, acetone, various mercaptans, various halogenated hydrocarbons such as carbon tetrachloride, and cyclohexane.

[0344] Bromine compounds or iodine compounds may be used as chain transfer agents. Polymerization methods using bromine compounds or iodine compounds include, for example, a method of polymerizing fluoromonomers in an aqueous medium in the presence of a bromine compound or an iodine compound in a substantially oxygen-free state (iodine transfer polymerization method). Representative examples of the bromine compounds or iodine compounds used include, for example, compounds represented by the general formula: R a I x Br y (wherein x and y are each an integer of 0 to 2 and satisfy 1≦x+y≦2; R ais a saturated or unsaturated fluorohydrocarbon group or chlorofluorohydrocarbon group having 1 to 16 carbon atoms, or a hydrocarbon group having 1 to 3 carbon atoms, which may contain an oxygen atom). By using a bromine compound or an iodine compound, iodine or bromine is introduced into the polymer and functions as a crosslinking point.

[0345] Examples of bromine compounds or iodine compounds include 1,3-diiodoperfluoropropane, 2-iodoperfluoropropane, 1,3-diiodo-2-chloroperfluoropropane, 1,4-diiodoperfluorobutane, 1,5-diiodo-2,4-dichloroperfluoropentane, 1,6-diiodoperfluorohexane, 1,8-diiodoperfluorooctane, 1,12-diiodoperfluorododecane, 1,16-diiodoperfluorohexadecane, diiodomethane, 1,2-diiodoethane, 1,3-diiodo-n-propane, CF2Br2, BrCF2CF2Br, CF3CFBrCF2Br, CFClBr2, BrCF2 Examples include CFClBr, CFBrClCFClBr, BrCFCFCFBr, BrCFCFBrOCF, 1-bromo-2-iodoperfluoroethane, 1-bromo-3-iodoperfluoropropane, 1-bromo-4-iodoperfluorobutane, 2-bromo-3-iodoperfluorobutane, 3-bromo-4-iodoperfluorobutene-1, 2-bromo-4-iodoperfluorobutene-1, monoiodomonobromo-substituted benzene, diiodomonobromo-substituted benzene, and (2-iodoethyl) and (2-bromoethyl) substituted benzenes. These compounds may be used alone or in combination with each other.

[0346] Among these, it is preferable to use 1,4-diiodoperfluorobutane, 1,6-diiodoperfluorohexane, and 2-iodoperfluoropropane in terms of polymerization reactivity, crosslinking reactivity, availability, and the like.

[0347] The amount of the chain transfer agent used is usually 1 to 50,000 ppm by mass, and preferably 1 to 20,000 ppm by mass, based on the total amount of fluoromonomers supplied.

[0348] The chain transfer agent may be added all at once to the reaction vessel before the initiation of polymerization, may be added all at once after the initiation of polymerization, may be added in multiple divided portions during the polymerization, or may be added continuously during the polymerization.

[0349] As the polymerization initiator, persulfates (e.g., ammonium persulfate), or organic peroxides such as disuccinic acid peroxide and diglutaric acid peroxide can be used alone or in the form of a mixture thereof. They may also be used in combination with a reducing agent such as sodium sulfite to form a redox system. Furthermore, during polymerization, a radical scavenger such as hydroquinone or catechol, or a peroxide decomposer such as ammonium sulfite, can be added to adjust the radical concentration in the system.

[0350] In the above polymerization, a fluoromonomer may be polymerized in an aqueous medium in the presence of polymer (I) to produce an aqueous dispersion of fluoropolymer particles, and the fluoromonomer may be seed-polymerized to the fluoropolymer particles in the aqueous dispersion of fluoropolymer particles to obtain a fluoropolymer.

[0351] The polymerization is preferably carried out by polymerizing a fluoromonomer substantially in the absence of a fluorine-containing surfactant (excluding compounds having a functional group reactive in radical polymerization and a hydrophilic group). Conventionally, a fluorine-containing surfactant has been used for polymerizing a fluoromonomer in an aqueous medium, but according to the production method of the present disclosure, a fluoropolymer can be obtained even without using a fluorine-containing surfactant.

[0352] In the present disclosure, "substantially in the absence of a fluorine-containing surfactant" means that the amount of the fluorine-containing surfactant relative to the aqueous medium is 10 ppm by mass or less. The amount of the fluorine-containing surfactant relative to the aqueous medium is preferably 1 ppm by mass or less, more preferably 100 ppb by mass or less, even more preferably 10 ppb by mass or less, and still more preferably 1 ppb by mass or less.

[0353] Examples of the fluorine-containing surfactant include anionic fluorine-containing surfactants, etc. The anionic fluorine-containing surfactant may be, for example, a surfactant containing fluorine atoms and having a total carbon number of 20 or less excluding the anionic group.

[0354] The fluorine-containing surfactant may also be a surfactant containing fluorine in the anionic moiety having a molecular weight of 1,000 or less, preferably 800 or less. The "anionic portion" refers to the portion of the fluorine-containing surfactant excluding the cation. For example, F(CF2) represented by the formula (I) below n1 In the case of COOM, "F(CF2) n1 The "COO" part.

[0355] The above-mentioned fluorine-containing surfactant also includes a fluorine-containing surfactant having a LogPOW of 3.5 or less. The LogPOW of the fluorine-containing surfactant is preferably 3.4 or less. The LogPOW is a partition coefficient between 1-octanol and water, and is expressed as LogP (where P represents the ratio of the fluorine-containing surfactant concentration in octanol to the fluorine-containing surfactant concentration in water when a 1:1 octanol / water mixture containing the fluorine-containing surfactant undergoes phase separation). The LogPOW is calculated from the HPLC elution time of the sample solution using standard substances (heptanoic acid, octanoic acid, nonanoic acid, and decanoic acid) with known octanol / water partition coefficients under the following conditions: column: TOSOH ODS-120T column (φ4.6 mm×250 mm, manufactured by Tosoh Corporation), eluent: acetonitrile / 0.6% by mass HClO₄ / water=1 / 1 (vol / vol%), flow rate: 1.0 mL / min, sample amount: 300 μL, column temperature: 40°C, detection light: UV 210 nm. A calibration curve between each elution time and the known octanol / water partition coefficient is then prepared, and the LogPOW is calculated from the HPLC elution time of the sample solution based on this calibration curve.

[0356] Specific examples of the fluorine-containing surfactants include those described in U.S. Patent Application Publication Nos. 2007 / 0015864, 2007 / 0015865, 2007 / 0015866, 2007 / 0276103, 2007 / 0117914, 2007 / 142541, 2008 / 0015319, and U.S. Pat. No. 3,250,808. No. 3,271,341, JP 2003-119204 A, WO 2005 / 042593, WO 2008 / 060461, WO 2007 / 046377, JP 2007-119526 A, WO 2007 / 046482, WO 2007 / 046345, U.S. Patent Application Publication No. 2014 / 0228531, WO 2013 / 189824, and WO 2013 / 189826.

[0357] The anionic fluorine-containing surfactant may be a compound represented by the following general formula (N 0 ): X n0 -Rf n0 -Y 0 (N 0 ) (In the formula, X n0 is H, Cl or F. n0is a linear, branched or cyclic alkylene group having 3 to 20 carbon atoms, in which some or all of the H's are substituted with F, and the alkylene group may contain one or more ether bonds, and some of the H's may be substituted with Cl. Y 0 is an anionic group. Y 0 The anionic group may be -COOM, -SO2M, or -SO3M, and may be -COOM or -SO3M. M is H, metal atom, NR 7 4. An optionally substituted imidazolium, an optionally substituted pyridinium, or an optionally substituted phosphonium, wherein R 7 is H or an organic group. The metal atom includes alkali metals (Group 1) and alkaline earth metals (Group 2), such as Na, K, or Li. R 7 As for H or C 1-10 may be an organic group of H or C 1-4 may be an organic group of H or C 1-4 The alkyl group may be: M is H, a metal atom, or NR 7 4, and may be H, an alkali metal (Group 1), an alkaline earth metal (Group 2), or NR 7 4, which may be H, Na, K, Li, or NH4. Above Rf n0 may be one in which 50% or more of H is substituted with fluorine.

[0358] The general formula (N 0 ) as a compound represented by The following general formula (N 1 ): X n0 -(CF2) m1 -Y 0 (N 1 ) (In the formula, X n0 is H, Cl, or F, m1 is an integer of 3 to 15, and Y 0is as defined above, a compound represented by the following general formula (N 2 ): Rf n1 -O-(CF(CF3)CF2O) m2 CFX n1 -Y 0 (N 2 ) (In the formula, Rf n1 is a perfluoroalkyl group having 1 to 5 carbon atoms, m2 is an integer of 0 to 3, and X n1 is F or CF3, and Y 0 is as defined above, a compound represented by the following general formula (N 3 ): Rf n2 (CH2) m3 -(Rf n3 ) q -Y 0 (N 3 ) (In the formula, Rf n2 is a partially or fully fluorinated alkyl group having 1 to 13 carbon atoms which may contain an ether bond, m3 is an integer of 1 to 3, and Rf n3 is a linear or branched perfluoroalkylene group having 1 to 3 carbon atoms, q is 0 or 1, and Y 0 is as defined above, a compound represented by the following general formula (N 4 ): Rf n4 -O-(CY n1 Y n2 ) p CF2-Y 0 (N 4 ) (In the formula, Rf n4 is a linear or branched partially or fully fluorinated alkyl group having 1 to 12 carbon atoms, which may contain an ether bond and / or a chlorine atom, and Y n1 and Y n2 are the same or different and are H or F, p is 0 or 1, and Y 0 is as defined above.) and a compound represented by the general formula (N 5 ): [ka] (In the formula, X n2 , X n3 and X n4 Rf may be the same or different and are H, F, or a linear or branched partially or fully fluorinated alkyl group having 1 to 6 carbon atoms, which may contain an ether bond. n5 is a linear or branched partially or fully fluorinated alkylene group having 1 to 3 carbon atoms, which may contain an ether bond; L is a linking group; Y 0 is as defined above, where X n2 , X n3 , X n4 and Rf n5 The total number of carbon atoms is 18 or less.

[0359] The general formula (N 0 ) More specifically, the compounds represented by the formula (I) include perfluorocarboxylic acids (I) represented by the following general formula (I), ω-H perfluorocarboxylic acids (II) represented by the following general formula (II), perfluoroethercarboxylic acids (III) represented by the following general formula (III), perfluoroalkyl alkylenecarboxylic acids (IV) represented by the following general formula (IV), perfluoroalkoxy fluorocarboxylic acids (V) represented by the following general formula (V), perfluoroalkyl sulfonic acids (VI) represented by the following general formula (VII), ω-H perfluorosulfonic acids (VII) represented by the following general formula (VII), perfluoroalkyl alkylene sulfonic acids (VIII) represented by the following general formula (VIII), alkyl alkylene carboxylic acids (IX) represented by the following general formula (IX), fluorocarboxylic acids (X) represented by the following general formula (X), alkoxy fluorosulfonic acids (XI) represented by the following general formula (XI), compounds (XII) represented by the following general formula (XII), and compounds (XIII) represented by the following general formula (XIII).

[0360] The perfluorocarboxylic acid (I) is represented by the following general formula (I): F(CF2) n1 COOM (I) (wherein n1 is an integer of 3 to 14, and M is H, a metal atom, or NR 7 4. An optionally substituted imidazolium, an optionally substituted pyridinium, or an optionally substituted phosphonium, wherein R 7 is H or an organic group.

[0361] The ω-H perfluorocarboxylic acid (II) is represented by the following general formula (II): H(CF2) n2 COOM (II) (wherein n2 is an integer of 4 to 15, and M is as defined above).

[0362] The perfluoroether carboxylic acid (III) is represented by the following general formula (III): Rf 1 -O-(CF(CF3)CF2O) n3 CF(CF3)COOM (III) (In the formula, Rf 1 is a perfluoroalkyl group having 1 to 5 carbon atoms, n3 is an integer of 0 to 3, and M is as defined above.

[0363] The perfluoroalkyl alkylene carboxylic acid (IV) is represented by the following general formula (IV): Rf 2 (CH2) n4 Rf 3 COOM (IV) (In the formula, Rf 2 is a perfluoroalkyl group having 1 to 5 carbon atoms, and Rf 3 is a linear or branched perfluoroalkylene group having 1 to 3 carbon atoms, n4 is an integer of 1 to 3, and M is as defined above.

[0364] The alkoxyfluorocarboxylic acid (V) is represented by the following general formula (V): Rf 4 -O-CY 1 Y 2 CF2-COOM (V) (In the formula, Rf 4 is a linear or branched partially or fully fluorinated alkyl group having 1 to 12 carbon atoms, which may contain an ether bond and / or a chlorine atom, and Y 1 and Y 2 are the same or different and are H or F, and M is as defined above.

[0365] The perfluoroalkylsulfonic acid (VI) is represented by the following general formula (VI): F(CF2) n5 SO3M (VI) (wherein n5 is an integer of 3 to 14, and M is as defined above).

[0366] The ω-H perfluorosulfonic acid (VII) is represented by the following general formula (VII): H(CF2) n6 SO3M (VII) (wherein n6 is an integer of 4 to 14, and M is as defined above).

[0367] The perfluoroalkyl alkylene sulfonic acid (VIII) is represented by the following general formula (VIII): Rf 5 (CH2) n7 SO3M (VIII) (In the formula, Rf 5 is a perfluoroalkyl group having 1 to 13 carbon atoms, n7 is an integer of 1 to 3, and M is as defined above.

[0368] The alkyl alkylene carboxylic acid (IX) is represented by the following general formula (IX): Rf 6 (CH2) n8 COOM (IX) (In the formula, Rf 6 is a linear or branched partially or fully fluorinated alkyl group having 1 to 13 carbon atoms which may contain an ether bond, n8 is an integer of 1 to 3, and M is as defined above.

[0369] The fluorocarboxylic acid (X) is represented by the following general formula (X): Rf 7 -O-Rf 8 -O-CF2-COOM (X) (In the formula, Rf 7 is a linear or branched partially or fully fluorinated alkyl group having 1 to 6 carbon atoms, which may contain an ether bond and / or a chlorine atom, and Rf 8 is a linear or branched, partially or fully fluorinated alkyl group having 1 to 6 carbon atoms, and M is as defined above.

[0370] The alkoxyfluorosulfonic acid (XI) is represented by the following general formula (XI): Rf 9 -O-CY 1 Y 2 CF2-SO3M (XI) (In the formula, Rf 9 is a linear or branched alkyl group having 1 to 12 carbon atoms, which may contain an ether bond, and which may contain chlorine, and which is partially or completely fluorinated; Y 1 and Y 2 are the same or different and are H or F, and M is as defined above.

[0371] The compound (XII) is represented by the following general formula (XII): [ka] (In the formula, X 1 , X 2 and X 3 may be the same or different and are H, F and linear or branched partially or fully fluorinated alkyl groups having 1 to 6 carbon atoms which may contain ether bonds; Rf 10 is a perfluoroalkylene group having 1 to 3 carbon atoms, L is a linking group, and Y 0 is an anionic group. Y 0may be -COOM, -SO2M, or -SO3M, and may be -SO3M or COOM (wherein M is as defined above). Examples of L include a single bond and a partially or fully fluorinated alkylene group having 1 to 10 carbon atoms which may contain an ether bond.

[0372] The compound (XIII) is represented by the following general formula (XIII): Rf 11 -O-(CF2CF(CF3)O) n9 (CF2O) n10 CF2COOM (XIII) (In the formula, Rf 11 is a fluoroalkyl group containing chlorine and having 1 to 5 carbon atoms, n9 is an integer of 0 to 3, n10 is an integer of 0 to 3, and M is as defined above. Compound (XIII) is represented by the formula: CF2ClO(CF2CF(CF3)O) n9 (CF2O) n10 CF2COONH4 (a mixture having an average molecular weight of 750, wherein n9 and n10 are defined above).

[0373] As mentioned above, examples of the anionic fluorine-containing surfactant include carboxylic acid surfactants and sulfonic acid surfactants.

[0374] The fluorine-containing surfactant may be one type of fluorine-containing surfactant or a mixture containing two or more types of fluorine-containing surfactants.

[0375] Examples of the fluorine-containing surfactant include compounds represented by the following formula: The fluorine-containing surfactant may be a mixture of these compounds: In one embodiment of the above polymerization, the fluoromonomer is polymerized substantially in the absence of a compound represented by the following formula: F(CF2)7COOM, F(CF2)5COOM, H(CF2)6COOM, H(CF2)7COOM, CF3O(CF2)3OCHFCF2COOM, C3F7OCF(CF3)CF2OCF(CF3)COOM, CF3CF2CF2OCF(CF3)COOM, CF3CF2OCF2CF2OCF2COOM, C2F5OCF(CF3)CF2OCF(CF3)COOM, CF3OCF(CF3)CF2OCF(CF3)COOM, CF2ClCF2CF2OCF(CF3)CF2OCF2COOM, CF2ClCF2CF2OCF2CF(CF3)OCF2COOM, CF2ClCF(CF3)OCF(CF3)CF2OCF2COOM, CF2ClCF(CF3)OCF2CF(CF3)OCF2COOM, [ka] (In each formula, M is H, metal atom, NR 7 4. An imidazolium which may have a substituent, a pyridinium which may have a substituent, or a phosphonium which may have a substituent. 7 is H or an organic group.

[0376] The aqueous medium used in the production method of the present disclosure refers to a liquid containing water. The aqueous medium is not particularly limited as long as it contains water, and may contain water and, for example, a fluorine-free organic solvent such as an alcohol, ether, or ketone, and / or a fluorine-containing organic solvent having a boiling point of 40° C. or lower.

[0377] Polymerization of the fluoromonomer in the aqueous medium gives an aqueous dispersion containing a fluoropolymer, polymer (I), and the aqueous medium. The fluoropolymer content (solids concentration) in the aqueous dispersion is usually 8 to 50 mass%, preferably 10 mass% or more, more preferably 15 mass% or more, preferably 40 mass% or more, and more preferably 35 mass% or less.

[0378] The fluoropolymer content in the aqueous dispersion is a value obtained by drying 1 g of the aqueous dispersion in a blower dryer at 150°C for 60 minutes, measuring the mass of the heating residue, and calculating the ratio of the mass of the heating residue to the mass (1 g) of the aqueous dispersion as a percentage.

[0379] In the manufacturing method of the present disclosure, the aqueous dispersion obtained by polymerizing the fluoromonomer in the aqueous medium may be subjected to the fluorine radical treatment as a composition, or the obtained aqueous dispersion may be coagulated to obtain a composition containing the fluoropolymer and the polymer (I), and then the composition may be subjected to the fluorine radical treatment.

[0380] Examples of methods for coagulating an aqueous dispersion include diluting the aqueous dispersion with water to a fluoropolymer concentration of 5 to 20% by mass, adjusting the pH to neutral or alkaline in some cases, and then stirring more vigorously than during the reaction in a vessel equipped with a stirrer; and adding a coagulant to the aqueous dispersion, such as a water-soluble organic compound such as methanol or acetone, an inorganic salt such as potassium nitrate or ammonium carbonate, or an inorganic acid such as hydrochloric acid, sulfuric acid, or nitric acid. When coagulating using a coagulant, the aqueous dispersion may be stirred. The aqueous dispersion may also be continuously stirred using an in-line mixer or the like.

[0381] The concentration of uncoagulated fluoropolymer in the wastewater resulting from coagulation is preferably low from the viewpoint of productivity, more preferably less than 0.4 mass %, particularly preferably less than 0.3 mass %.

[0382] By coagulating the aqueous dispersion, a composition containing a fluoropolymer, polymer (I) and water is usually obtained, and the obtained composition may be dried using a method such as vacuum, high frequency, or the above-mentioned heat treatment to obtain a composition. When the composition contains PTFE as the fluoropolymer, it is preferable to dry the composition while keeping it in a state where it is not very fluid, preferably while it is left standing, in order to suppress fibrillation of PTFE.

[0383] In one embodiment of the composition to be subjected to the fluorine radical treatment, it contains a fluorine-containing surfactant. Even when the composition contains a fluorine-containing surfactant, impurities in the composition can be reduced by the fluorine radical treatment.

[0384] In one embodiment of the composition to be subjected to fluorine radical treatment, it is substantially free of fluorine-containing surfactant. Furthermore, in one embodiment of the high-purity fluoropolymer-containing composition, it is also substantially free of fluorine-containing surfactant. In the present disclosure, "substantially free of fluorine-containing surfactant" means that the content of fluorine-containing surfactant in the composition is 10 ppm by mass or less, preferably 1 ppm by mass or less, more preferably 100 ppb by mass or less, even more preferably 10 ppb by mass or less, still more preferably 1 ppb by mass or less, and particularly preferably below the detection limit of fluorine-containing surfactant as measured by liquid chromatography-mass spectrometry (LC / MS).

[0385] The content of the fluorine-containing surfactant can be measured, for example, by adding methanol to the composition, extracting it, and analyzing the resulting extract by LC / MS. To further increase the extraction efficiency, treatment such as Soxhlet extraction or ultrasonic treatment may be carried out. Molecular weight information is extracted from the obtained LC / MS spectrum and confirmed to match the structural formula of the candidate fluorine-containing surfactant. Then, aqueous solutions containing five or more levels of the identified fluorine-containing surfactant are prepared, and LC / MS analysis is performed on the aqueous solutions containing each level. The relationship between the content and the area corresponding to that content is plotted, and a calibration curve is drawn. Then, using the calibration curve, the area of ​​the LC / MS chromatogram of the fluorine-containing surfactant in the extract can be converted into the content of the fluorine-containing surfactant.

[0386] (fluoropolymer) Examples of fluoropolymers include TFE polymers in which the monomer having the largest molar fraction in the polymer (hereinafter referred to as the "most abundant monomer") is TFE, VDF polymers in which the most abundant monomer is VDF, and CTFE polymers in which the most abundant monomer is CTFE.

[0387] The fluoropolymers preferably have an ion exchange ratio (IXR) greater than 53. Preferred fluoropolymers have no ionic groups or a limited number of ionic groups resulting in an ion exchange ratio greater than about 100. Preferred fluoropolymers preferably have an ion exchange ratio of 1000 or greater, more preferably 2000 or greater, and even more preferably 5000 or greater.

[0388] The TFE polymer may suitably be a TFE homopolymer or a copolymer comprising (1) TFE, (2) one or more fluorine-containing monomers other than TFE having 2 to 8 carbon atoms, particularly VDF, HFP, or CTFE, and (3) other monomers. Examples of the (3) other monomers include fluoro(alkyl vinyl ethers) having an alkyl group having 1 to 5 carbon atoms, particularly 1 to 3 carbon atoms; fluorodioxole; perfluoroalkylethylene; and ω-hydroperfluoroolefin.

[0389] The TFE polymer may also be a copolymer of TFE and one or more fluorine-free monomers. Examples of the fluorine-free monomers include alkenes such as ethylene and propylene; vinyl esters; and vinyl ethers. The TFE polymer may also be a copolymer of TFE and one or more fluorine-containing monomers having 2 to 8 carbon atoms and one or more fluorine-free monomers.

[0390] The VDF polymer may suitably be a VDF homopolymer [PVDF] or a copolymer of (1) VDF, (2) one or more fluoroolefins other than VDF having 2 to 8 carbon atoms, particularly TFE, HFP, or CTFE, and (3) a perfluoro(alkyl vinyl ether) having an alkyl group having 1 to 5 carbon atoms, particularly 1 to 3 carbon atoms.

[0391] The CTFE polymer may suitably be a CTFE homopolymer or a copolymer consisting of (1) CTFE, (2) one or more fluoroolefins other than CTFE having 2 to 8 carbon atoms, particularly TFE or HFP, and (3) a perfluoro(alkyl vinyl ether) having an alkyl group having 1 to 5 carbon atoms, particularly 1 to 3 carbon atoms.

[0392] The CTFE polymer may also be a copolymer of CTFE and one or more non-fluorine-containing monomers, and the non-fluorine-containing monomers include alkenes such as ethylene and propylene; vinyl esters; and vinyl ethers.

[0393] The fluoropolymers may be glassy, ​​plastic or elastomeric. They may be amorphous or partially crystalline and may be subject to compression-sintering, melt-processing or non-melt-processing.

[0394] In the production method of the present disclosure, for example, (I) tetrafluoroethylene polymer [TFE polymer (PTFE)] can be suitably produced as a non-melt-processable fluororesin, and (II) TFE / HFP copolymer [FEP], TFE / perfluoro(alkyl vinyl ether) copolymer [PFA, MFA, etc.], TFE / perfluoroallyl ether copolymer, electrolyte polymer precursor, etc. can be suitably produced as a melt-processable fluororesin.

[0395] The fluoropolymer is preferably a fluororesin, and particularly, a fluororesin having a fluorine substitution rate of 50% or more as calculated by the following formula is more preferred, a fluororesin having a fluorine substitution rate of more than 50% is even more preferred, a fluororesin having a fluorine substitution rate of 55% or more is even more preferred, a fluororesin having a fluorine substitution rate of 60% or more is even more preferred, a fluororesin having a fluorine substitution rate of 75% or more is even more preferred, a fluororesin having a fluorine substitution rate of 80% or more is particularly preferred, and a fluororesin having a fluorine substitution rate of 90 to 100%, i.e., a perfluororesin, is most preferred. (formula) Fluorine substitution rate (%) = (number of fluorine atoms bonded to carbon atoms constituting the fluoropolymer) / ((number of hydrogen atoms bonded to carbon atoms constituting the fluoropolymer) + (number of fluorine atoms and chlorine atoms bonded to carbon atoms constituting the fluoropolymer)) × 100

[0396] The perfluororesin is more preferably a fluororesin having a fluorine substitution rate of 95 to 100%, further preferably PTFE, FEP or PFA, and particularly preferably PTFE.

[0397] The fluoropolymer may have a core-shell structure. Examples of the fluoropolymer having a core-shell structure include modified PTFE particles containing a core of high molecular weight PTFE and a shell of lower molecular weight PTFE or modified PTFE. Examples of such modified PTFE include the PTFE described in JP-A-2005-527652.

[0398] The core-shell structure may have the following structure. Core: TFE homopolymer Shell: TFE homopolymer Core: Modified PTFE Shell: TFE homopolymer Core: Modified PTFE Shell: Modified PTFE Core: TFE homopolymer Shell: Modified PTFE Core: Low molecular weight PTFE Shell: High molecular weight PTFE Core: High molecular weight PTFE Shell: Low molecular weight PTFE

[0399] In the fluoropolymer having the core-shell structure, the lower limit of the core ratio is preferably 0.5 mass%, more preferably 1.0 mass%, even more preferably 3.0 mass%, particularly preferably 5.0 mass%, and most preferably 10.0 mass%. The upper limit of the core ratio is preferably 99.5 mass%, more preferably 99.0 mass%, even more preferably 98.0 mass%, even more preferably 97.0 mass%, particularly preferably 95.0 mass%, and most preferably 90.0 mass%.

[0400] In the fluoropolymer having the core-shell structure, the lower limit of the shell ratio is preferably 0.5% by mass, more preferably 1.0% by mass, even more preferably 3.0% by mass, particularly preferably 5.0% by mass, and most preferably 10.0% by mass. The upper limit of the shell ratio is preferably 99.5% by mass, more preferably 99.0% by mass, even more preferably 98.0% by mass, even more preferably 97.0% by mass, particularly preferably 95.0% by mass, and most preferably 90.0% by mass.

[0401] In the fluoropolymer having the core-shell structure, the core or the shell may be configured to have two or more layers. For example, the fluoropolymer may have a three-layer structure having a core center portion of modified PTFE, a core outer layer portion of TFE homopolymer, and a shell of modified PTFE.

[0402] The fluoropolymer having the core-shell structure also includes a particle of the fluoropolymer having multiple cores.

[0403] The above-mentioned (I) non-melt-processible fluororesin and (II) melt-processible fluororesin, which are suitably produced by the production method of the present disclosure, are preferably produced in the following manner.

[0404] (I) Non-melt-processable fluororesin In the production method of the present disclosure, TFE polymerization is usually carried out at a polymerization temperature of 10 to 150°C and a polymerization pressure of 0.05 to 5 MPaG. For example, the polymerization temperature is more preferably 30°C or higher, and even more preferably 50°C or higher. It is more preferably 120°C or lower, and even more preferably 100°C or lower. The polymerization pressure is more preferably 0.3 MPaG or higher, and even more preferably 0.5 MPaG or higher, and more preferably 5.0 MPaG or lower, and even more preferably 3.0 MPaG or lower. In particular, from the viewpoint of improving the yield of the fluoropolymer, it is preferably 1.0 MPaG or higher, more preferably 1.2 MPaG or higher, more preferably 1.5 MPaG or higher, and even more preferably 2.0 MPaG or higher.

[0405] In one embodiment, the polymerization is carried out by charging pure water into a pressure-resistant reaction vessel equipped with a stirrer, deoxidizing, then charging TFE, adjusting the temperature to a predetermined level, and adding a polymerization initiator to initiate the reaction. If the pressure decreases as the reaction proceeds, additional TFE is continuously or intermittently supplied to maintain the initial pressure. Once a predetermined amount of TFE has been supplied, the supply is stopped, the TFE in the reaction vessel is purged, and the temperature is returned to room temperature to terminate the reaction. Additional TFE may be continuously or intermittently supplied to prevent a decrease in pressure.

[0406] In the production of the TFE polymer (PTFE), various known modified monomers can also be used in combination. In the present disclosure, the TFE polymer is a concept that includes not only a TFE homopolymer but also a copolymer of TFE and a modified monomer that is not melt-processable (hereinafter referred to as "modified PTFE").

[0407] The modifying monomer is not particularly limited as long as it is copolymerizable with TFE, and examples thereof include fluoromonomers and non-fluoromonomers. The modifying monomer used may be one type or multiple types.

[0408] The non-fluoromonomer is not particularly limited and may be selected from the group consisting of monomers having the general formula: CH2=CR Q1 -LR Q2 (In the formula, R Q1 represents a hydrogen atom or an alkyl group. L represents a single bond, -CO-O-*, -O-CO-* or -O-. * represents R Q2 R represents the bond position with Q2 represents a hydrogen atom, an alkyl group or a nitrile group.

[0409] Examples of non-fluoromonomers include methyl acrylate, methyl methacrylate, ethyl acrylate, ethyl methacrylate, propyl acrylate, propyl methacrylate, butyl acrylate, butyl methacrylate, hexyl methacrylate, cyclohexyl methacrylate, vinyl methacrylate, vinyl acetate, acrylic acid, methacrylic acid, acrylonitrile, methacrylonitrile, ethyl vinyl ether, cyclohexyl vinyl ether, etc. Of these, butyl methacrylate, vinyl acetate, and acrylic acid are preferred as non-fluoromonomers.

[0410] Examples of fluoromonomers include perfluoroolefins such as hexafluoropropylene (HFP); hydrogen-containing fluoroolefins such as trifluoroethylene and vinylidene fluoride (VDF); perhaloolefins such as chlorotrifluoroethylene; perfluorovinyl ethers; (perfluoroalkyl)ethylenes; and perfluoroallyl ethers.

[0411] The perfluorovinyl ether is not particularly limited, and examples thereof include perfluorovinyl ethers represented by the general formula (A): CF2=CF-ORf (A) (wherein Rf represents a perfluoroorganic group). In the present disclosure, the "perfluoroorganic group" refers to an organic group in which all hydrogen atoms bonded to carbon atoms are substituted with fluorine atoms. The perfluoroorganic group may have an ether oxygen.

[0412] An example of the perfluorovinyl ether is perfluoro(alkyl vinyl ether) [PAVE], where Rf in general formula (A) is a perfluoroalkyl group having 1 to 10 carbon atoms. The number of carbon atoms in the perfluoroalkyl group is preferably 1 to 5.

[0413] Examples of the perfluoroalkyl group in the PAVE include a perfluoromethyl group, a perfluoroethyl group, a perfluoropropyl group, a perfluorobutyl group, a perfluoropentyl group, and a perfluorohexyl group.

[0414] The perfluorovinyl ether further includes those in which Rf in the general formula (A) is a perfluoro(alkoxyalkyl) group having 4 to 9 carbon atoms, and those in which Rf ...

[0415] [ka]

[0416] (wherein m represents 0 or an integer of 1 to 4), and Rf is a group represented by the following formula:

[0417] CF3CF2CF2-(O-CF(CF3)-CF2) n - (wherein n represents an integer of 1 to 4).

[0418] Examples of hydrogen-containing fluoroolefins include CH2=CF2, CFH=CH2, CFH=CF2, CH2=CFCF3, CH2=CHCF3, CHF=CHCF3 (E-isomer), and CHF=CHCF3 (Z-isomer).

[0419] The (perfluoroalkyl)ethylene (PFAE) is not particularly limited, and examples thereof include (perfluorobutyl)ethylene (PFBE) and (perfluorohexyl)ethylene.

[0420] Examples of perfluoroallyl ethers include: General formula: CF2=CF-CF2-ORf (wherein Rf represents a perfluoro organic group).

[0421] Rf in the above general formula is the same as Rf in general formula (A). Rf is preferably a perfluoroalkyl group having 1 to 10 carbon atoms or a perfluoroalkoxyalkyl group having 1 to 10 carbon atoms. The perfluoroallyl ether is preferably at least one selected from the group consisting of CF2=CF-CF2-O-CF3, CF2=CF-CF2-O-C2F5, CF2=CF-CF2-O-C3F7, and CF2=CF-CF2-O-C4F9, more preferably at least one selected from the group consisting of CF2=CF-CF2-O-C2F5, CF2=CF-CF2-O-C3F7, and CF2=CF-CF2-O-C4F9, and even more preferably CF2=CF-CF2-O-CF2CF2CF3.

[0422] A preferred example of the modifying monomer is the modifying monomer (3) having a monomer reactivity ratio of 0.1 to 8. The presence of the modifying monomer (3) makes it possible to obtain PTFE particles having a small particle size and an aqueous dispersion with high dispersion stability.

[0423] Here, the monomer reactivity ratio in copolymerization with TFE is the value obtained by dividing the rate constant when the propagating radical reacts with TFE when the propagating radical is less than a repeating unit based on TFE by the rate constant when the propagating radical reacts with the modified monomer. The lower this value, the higher the reactivity of the modified monomer with TFE. The monomer reactivity ratio can be calculated by copolymerizing TFE and the modified monomer, determining the composition in the resulting polymer immediately after the start of copolymerization, and using the Feynman-Ross equation.

[0424] The copolymerization was carried out in a 6.0 L stainless steel autoclave using 3600 g of deionized and degassed water, 1000 ppm by mass of ammonium perfluorooctanoate relative to the water, and 100 g of paraffin wax at a pressure of 0.78 MPaG and a temperature of 70°C. 0.05 g, 0.1 g, 0.2 g, 0.5 g, and 1.0 g of the modified monomer were added to the reactor, respectively, and 0.072 g of ammonium persulfate (20 ppm by mass relative to the water) was added. TFE was continuously fed to maintain the polymerization pressure at 0.78 MPaG. When the TFE charge reached 1000 g, stirring was stopped and the reactor was depressurized until atmospheric pressure was reached. After cooling, the paraffin wax was separated to obtain an aqueous dispersion containing the resulting polymer. The aqueous dispersion was stirred to coagulate the resulting polymer, which was then dried at 150°C. The composition of the resulting polymer is calculated by appropriately combining NMR, FT-IR, elemental analysis, and X-ray fluorescence analysis depending on the type of monomer.

[0425] The modified monomer (3) having a monomer reactivity ratio of 0.1 to 8 is preferably at least one selected from the group consisting of modified monomers represented by formulas (3a) to (3d). CH2=CH-Rf 1 (3a) (In the formula, Rf 1 is a perfluoroalkyl group having 1 to 10 carbon atoms. CF2=CF-O-Rf 2 (3b) (In the formula, Rf 2 is a perfluoroalkyl group having 1 to 2 carbon atoms. CF2=CF-O-(CF2) n CF=CF2(3c) (wherein n is 1 or 2).

[0426] [ka] (In the formula, X 3 and X 4 is F, Cl or a methoxy group, and Y is of formula Y1 or Y2.

[0427] [ka] (In formula Y2, Z and Z′ are F or a fluorinated alkyl group having 1 to 3 carbon atoms.)

[0428] The content of the modifying monomer (3) units is preferably in the range of 0.00001 to 1.0% by mass relative to the total polymerized units of PTFE. The lower limit is more preferably 0.0001% by mass, more preferably 0.0005% by mass, even more preferably 0.001% by mass, and even more preferably 0.005% by mass. The upper limit is, in order of preference, 0.90%, 0.50%, 0.40%, 0.30%, 0.20%, 0.15%, 0.10%, 0.08%, 0.05%, and 0.01% by mass.

[0429] As the above-mentioned modified monomer, since it can obtain an aqueous dispersion with a small average primary particle diameter, a small aspect ratio of primary particles, and excellent stability, it is preferred to use at least one selected from the group consisting of hexafluoropropylene, chlorotrifluoroethylene, vinylidene fluoride, perfluoro(alkyl vinyl ether), perfluoroallyl ether, (perfluoroalkyl)ethylene, ethylene, and modified monomers having a functional group capable of reacting by radical polymerization and a hydrophilic group, and more preferred is at least one selected from the group consisting of hexafluoropropylene, perfluoro(alkyl vinyl ether) and perfluoroallyl ether.By using the above-mentioned modified monomer, it is possible to obtain an aqueous dispersion of PTFE with a smaller average primary particle diameter, a small aspect ratio of primary particles, and excellent dispersion stability.In addition, it is possible to obtain an aqueous dispersion with less uncoagulated polymer.

[0430] From the viewpoint of reactivity with TFE, the modifying monomer preferably contains at least one selected from the group consisting of hexafluoropropylene, perfluoro(alkyl vinyl ether), and (perfluoroalkyl)ethylene. More preferably, it contains at least one selected from the group consisting of hexafluoropropylene, perfluoro(methyl vinyl ether), perfluoro(propyl vinyl ether), (perfluorobutyl)ethylene, (perfluorohexyl)ethylene, and (perfluorooctyl)ethylene. The total amount of the hexafluoropropylene units, perfluoro(alkyl vinyl ether) units, and (perfluoroalkyl)ethylene units is preferably in the range of 0.00001 to 1% by mass relative to all polymerized units of PTFE. The lower limit of the total amount is more preferably 0.0001% by mass, more preferably 0.0005% by mass, even more preferably 0.001% by mass, and even more preferably 0.005% by mass. The upper limits are, in order of preference, 0.80%, 0.70%, 0.50%, 0.40%, 0.30%, 0.20%, 0.15%, 0.10%, 0.08%, 0.05%, and 0.01% by mass.

[0431] The above-mentioned modified monomer preferably includes a modified monomer having a functional group capable of reacting by radical polymerization and a hydrophilic group (hereinafter referred to as "modified monomer (A)").

[0432] The presence of the above-mentioned modifying monomer (A) can produce PTFE particles with a small primary particle size, and can produce an aqueous dispersion with high dispersion stability. It can also reduce the amount of uncoagulated polymer. Furthermore, it can reduce the aspect ratio of the primary particles.

[0433] The amount of the modified monomer (A) used is preferably more than an amount corresponding to 0.1 ppm by mass of the aqueous medium, more preferably more than 0.5 ppm by mass, even more preferably more than 1.0 ppm by mass, even more preferably 5 ppm by mass or more, and particularly preferably 10 ppm by mass or more. If the amount of the modified monomer (A) used is too small, the average primary particle size of the obtained PTFE may not be reduced. The amount of the modifying monomer (A) used may be within the above range, but the upper limit can be, for example, 5000 ppm by mass. In the above production method, the modifying monomer (A) may be added to the system during the reaction to improve the stability of the aqueous dispersion during or after the reaction.

[0434] The above-mentioned modified monomer (A) is highly water-soluble, so even if unreacted modified monomer (A) remains in the aqueous dispersion, it can be easily removed in the concentration step or the coagulation and washing step.

[0435] The above-mentioned modifying monomer (A) is incorporated into the produced polymer during the polymerization process, but since the concentration of the modifying monomer (A) itself in the polymerization system is low and the amount incorporated into the polymer is small, there are no problems such as a decrease in the heat resistance of PTFE or coloration after baking.

[0436] Examples of the hydrophilic group in the modified monomer (A) include -NH2, -PO3M, -OPO3M, -SO3M, -OSO3M, and -COOM (in each formula, M represents H, a metal atom, or NR 7y 4. An imidazolium which may have a substituent, a pyridinium which may have a substituent, or a phosphonium which may have a substituent, R 7y are H or organic groups and may be the same or different. Any two of them may be bonded to each other to form a ring. ) are examples of the hydrophilic group. Of these, -SO3M or -COOM is preferred. R 7y The organic group in R is preferably an alkyl group. 7y As for H or C 1-10 is preferably an organic group represented by the formula: 1-4 The organic group is more preferably H or C 1-4 More preferred are alkyl groups of the formula: The metal atom may be a monovalent or divalent metal atom, such as an alkali metal (Group 1) or an alkaline earth metal (Group 2), with Na, K, or Li being preferred.

[0437] Examples of the "functional group capable of reacting by radical polymerization" in the modifying monomer (A) include groups having an ethylenically unsaturated bond, such as a vinyl group and an allyl group. The group having an ethylenically unsaturated bond is a group represented by the following formula: CX e X g =CX f R- (In the formula, X e , X f and X g are each independently F, Cl, H, CF3, CF2H, CFH2, or CH3; and R is a linking group. The linking group for R can be represented by the formula: a Preferred linking groups include -CH=CH2 and -CF=CH 2、 -CH=CF 2、 Examples include groups having an unsaturated bond such as -CF=CF2, -CH2-CH=CH2, -CF2-CF=CH2, -CF2-CF=CF2, -(C=O)-CH=CH2, -(C=O)-CF=CH2, -(C=O)-CH=CF2, -(C=O)-CF=CF2, -(C=O)-C(CH3)=CH2, -(C=O)-C(CF3)=CH2, -(C=O)-C(CH3)=CF2, -(C=O)-C(CF3)=CF2, -O-CH2-CH=CH2, -O-CF2-CF=CH2, -O-CH2-CH=CF2, and -O-CF2-CF=CF2.

[0438] The modified monomer (A) has a functional group capable of reacting by radical polymerization, and therefore, when used in the polymerization, it is presumed that it reacts with the fluorine-containing monomer at the initial stage of the polymerization reaction, and forms highly stable particles having hydrophilic groups derived from the modified monomer (A). Therefore, it is considered that the number of particles increases when polymerization is carried out in the presence of the modified monomer (A).

[0439] The polymerization may be carried out in the presence of one type of the modifying monomer (A), or in the presence of two or more types thereof.

[0440] In the above polymerization, a compound having an unsaturated bond can be used as the modifying monomer (A).

[0441] The modifying monomer (A) is represented by the general formula (4): CX i X k =CX j R a -(CZ 1 Z 2 ) k -Y 3 (4) (In the formula, X i , X j and X k are each independently F, Cl, H, or CF; Y 3 is a hydrophilic group; R a is a linking group; Z 1 and Z 2 are each independently H, F or CF3, and k is 0 or 1). Examples of the hydrophilic group include -NH2, -PO3M, -OPO3M, -SO3M, -OSO3M, and -COOM (in each formula, M represents H, a metal atom, or NR 7y 4. An imidazolium which may have a substituent, a pyridinium which may have a substituent, or a phosphonium which may have a substituent, R 7y are H or organic groups and may be the same or different. Any two of them may be bonded to each other to form a ring. ) are examples of the hydrophilic group. Of these, -SO3M or -COOM is preferred. R 7y The organic group in R is preferably an alkyl group. 7y As for H or C 1-10 is preferably an organic group represented by the formula: 1-4 The organic group is more preferably H or C 1-4 More preferred are alkyl groups of the following formula: Examples of the metal atom include monovalent and divalent metal atoms, such as alkali metals (Group 1) and alkaline earth metals (Group 2), with Na, K or Li being preferred. By using the modifying monomer (A), an aqueous dispersion having a smaller average primary particle size and better stability can be obtained, and the aspect ratio of the primary particles can also be made smaller.

[0442] Above R a is a linking group. In the present disclosure, "linking group" refers to a divalent linking group. The linking group may be a single bond and preferably contains at least one carbon atom, and the number of carbon atoms may be 2 or more, 4 or more, 8 or more, 10 or more, or 20 or more. There is no upper limit, but it may be, for example, 100 or less, or 50 or less. The linking group may be linear or branched, cyclic or acyclic, saturated or unsaturated, substituted or unsubstituted, and may optionally contain one or more heteroatoms selected from the group consisting of sulfur, oxygen, and nitrogen, and may optionally contain one or more functional groups selected from the group consisting of ester, amide, sulfonamide, carbonyl, carbonate, urethane, urea, and carbamate. The linking group may not contain carbon atoms but may be a catenary heteroatom such as oxygen, sulfur, or nitrogen.

[0443] Above R a is preferably a catenary heteroatom such as oxygen, sulfur, or nitrogen, or a divalent organic group. R a When R is a divalent organic group, the hydrogen atom bonded to the carbon atom may be replaced with a halogen other than fluorine, such as chlorine, and may or may not contain a double bond. a may be either linear or branched, and may be either cyclic or acyclic. a may contain functional groups (e.g., esters, ethers, ketones, amines, halides, etc.). R a may also be a non-fluorinated divalent organic group, or a partially fluorinated or perfluorinated divalent organic group. R aExamples of the hydrocarbon group include a hydrocarbon group in which no fluorine atoms are bonded to a carbon atom, a hydrocarbon group in which some of the hydrogen atoms bonded to a carbon atom are substituted with fluorine atoms, a hydrocarbon group in which all of the hydrogen atoms bonded to a carbon atom are substituted with fluorine atoms, -(C=O)-, -(C=O)-O-, or a hydrocarbon group containing -(C=O)-, which may contain an oxygen atom, a double bond, or a functional group.

[0444] R a is preferably —(C═O)—, —(C═O)—O—, or a hydrocarbon group having 1 to 100 carbon atoms which may contain an ether bond and may contain a carbonyl group, and in the hydrocarbon group, some or all of the hydrogen atoms bonded to the carbon atoms may be substituted with fluorine. R a Preferably, -(CH2) a -, -(CF2) a -, -O-(CF2) a -, -(CF2) a -O-(CF2) b -, -O(CF2) a -O-(CF2) b -, -(CF2) a -[O-(CF2) b ] c -, -O(CF2) a -[O-(CF2) b ] c -, -[(CF2) a -O] b -[(CF2) c -O] d -, -O[(CF2) a -O] b -[(CF2) c -O] d -, -O-[CF2CF(CF3)O] a -(CF2) b -, -(C=O)-, -(C=O)-O-, -(C=O)-(CH2) a -, -(C=O)-(CF2) a -, -(C=O)-O-(CH2) a -, -(C=O)-O-(CF2) a-, -(C=O)-[(CH2) a -O] b -, -(C=O)-[(CF2) a -O] b -, -(C=O)-O[(CH2) a -O] b -, -(C=O)-O[(CF2) a -O] b -, -(C=O)-O[(CH2) a -O] b -(CH2) c -, -(C=O)-O[(CF2) a -O] b -(CF2) c -, -(C=O)-(CH2) a -O-(CH2) b -, -(C=O)-(CF2) a -O-(CF2) b -, -(C=O)-O-(CH2) a -O-(CH2) b -, -(C=O)-O-(CF2) a -O-(CF2) b At least one selected from -, -(C=O)-O-C6H4-, and combinations thereof. In the formula, a, b, c, and d are independently at least 1. a, b, c, and d may independently be 2 or more, 3 or more, 4 or more, 10 or more, or 20 or more. The upper limit of a, b, c, and d is, for example, 100.

[0445] R aSpecific examples suitable as -CF2-O-, -CF2-O-CF2-, -CF2-O-CH2-, -CF2-O-CH2CF2-, -CF2-O-CF2CF2-, -CF2-O-CF2CH2-, -CF2-O-CF2CF2CH2-, -CF2-O-CF(CF3)-, -CF2-O-CF(CF3) CF2-, -CF2-O-CF(CF3)CF2-O-, -CF2-O-CF(CF3)CH2-, -(C=O)-, -(C=O)-O-, -(C=O)- (CH2)-, -(C=O)-(CF2)-, -(C=O)-O-(CH2)-, -(C=O)-O-(CF2)-, -(C=O)-[(CH2)2-O] n -, -(C=O)-[(CF2)2-O] n -, -(C=O)-O[(CH2)2-O] n -, -(C=O)-O[(CF2)2-O] n -, -(C=O)-O[(CH2)2-O] n -(CH2)-, -(C=O)-O[(CF2)2-O] n -(CF2)-, -(C=O)-(CH2)2-O-(CH2)-, -(C=O)-(CF2)2-O-(CF2)-, -(C=O)-O-(CH2)2-O-(CH2)-, -(C=O)-O-(CF2)2-O-(CF2)-, -(C=O)-O-C6H4-, etc. a Specifically, -CF2-O-, -CF2-O-CF2-, -CF2-O-CF2CF2-, -CF2-O-CF(CF3)-, -CF2-O-CF(CF3)CF2-, -CF2 -O-CF(CF3)CF2-O-, -(C=O)-, -(C=O)-O-, -(C=O)-(CH2)-, -(C=O)-O-(CH2)-, -(C=O)-O[(CH2)2-O] n -, -(C=O)-O[(CH2)2-O] n -(CH2)-, -(C=O)-(CH2)2-O-(CH2)-, or -(C=O)-O-C6H4- is preferred. In the above formula, n is an integer of 1 to 10.

[0446] -R in general formula (4) a -(CZ 1 Z 2 )k -としては、-CF2-O-CF2-、-CF2-O-CF(CF3)-、-CF2-OC(CF3)2-、-CF2-O-CF2-CF2-、-CF2-O-CF2-CF(CF3)-、-CF2-O-CF2-C(CF3)2-、-CF2-O-CF2CF2-CF2-、-CF2-O-CF2CF2-CF (CF3)-、-CF2-O-CF2CF2-C(CF3)2-、-CF2-O-CF(CF3)-CF2-、-CF2-O-CF(CF3)-CF(CF 3)-、-CF2-O-CF(CF3)-C(CF3)2-、-CF2-O-CF(CF3)-CF2-、-CF2-O-CF(CF3)-CF(CF3) -、-CF2-O-CF(CF3)-C(CF3)2-、-CF2-O-CF(CF3)CF2-CF2-、-CF2-O-CF(CF3)CF2-CF( CF3)-、-CF2-O-CF(CF3)CF2-C(CF3)2-、-CF2-O-CF(CF3)CF2-O-CF2-、-CF2-O-CF(CF 3)CF2-O-CF(CF3)-、-CF2-O-CF(CF3)CF2-OC(CF3)2-、-(C=O)-、-(C=O)-O-、-(C=O)- (CH2)-、-(C=O)-(CF2)-、-(C=O)-O-(CH2)-、-(C=O)-O-(CF2)-、-(C=O)-[(CH2)2-O] n -(CH2)-、-(C=O)-[(CF2)2-O] n -(CF2)-、-(C=O)-[(CH2)2-O] n -(CH2)-(CH2)-、-(C=O)-[(CF2)2-O] n -(CF2)-(CF2)-、-(C=O)-O[(CH2)2-O] n -(CF2)-、-(C=O)-O[(CH2)2-O] n -(CH2)-(CH2)-、-(C=O)-O[(CF2)2-O] n -(CF2)-、-(C=O)-O[(CF2)2-O] n-(CF2)-(CF2)-, -(C=O)-(CH2)2-O-(CH2)-(CH2)-, -(C=O)-(CF2)2-O-(CF2)-(CF2)-, -(C=O)-O-(CH2)2-O-(CH2)-(CH2)-, -(C=O )-O-(CF2)2-O-(CF2)-(CF2)-, -(C=O)-O-(CH2)2-O-(CH2)-C(CF3)2-, -(C=O)-O-(CF2)2-O-(CF2)-C(CF3)2-, or -(C=O)-O-C6H4- C(CF3)2- is preferred, -CF2-O-CF(CF3)-, -CF2-O-CF2-CF(CF3)-, -CF2-O-CF2CF2-CF(CF3)-, -CF2-O-CF(CF3)-CF(CF3)-, -CF2-O-CF(C F3)CF2-CF(CF3)-, -CF2-O-CF(CF3)CF2-O-CF(CF3)-, -(C=O)-, -(C=O)-O-(CH2)-, -(C=O)-O-(CH2)-(CH2)-, -(C=O)-O[(CH2)2-O] n -(CH2)-(CH2)-, -(C=O)-O-(CH2)2-O-(CH2)-C(CF3)2-, or -(C=O)-O-C6H4-C(CF3)2- is more preferred. In the above formula, n is an integer of 1 to 10.

[0447] Specific examples of the compound represented by general formula (4) include: [ka] (In the formula, X j and Y 3 is the same as above. n is an integer of 1 to 10.

[0448] R a As the general formula (r1): -(C=O) h -(O) i -CF2-O-(CX 6 2) e -{O-CF(CF3)} f -(O) g - (r1) (In the formula, X 6are each independently H, F, or CF3, e is an integer of 0 to 3, f is an integer of 0 to 3, g is 0 or 1, h is 0 or 1, and i is 0 or 1), and a divalent group represented by the general formula (r2): -(C=O) h -(O) i -CF2-O-(CX 7 2) e -(O) g - (r2) (In the formula, X 7 are each independently H, F or CF3, e is an integer of 0 to 3, g is 0 or 1, h is 0 or 1, and i is 0 or 1. Divalent groups represented by the following formula are also preferred.

[0449] -R in general formula (4) a -(CZ 1 Z 2 ) k - can also be represented by the following formula (t1): -(C=O) h -(O) i -CF2-O-(CX 6 2) e -{O-CF(CF3)} f -(O) g -CZ 1 Z 2 - (t1) (In the formula, X 6 are each independently H, F, or CF3, e is an integer of 0 to 3, f is an integer of 0 to 3, g is 0 or 1, h is 0 or 1, i is 0 or 1, and Z 1 and Z 2 are each independently F or CF3), and in formula (t1), Z 1 and Z 2 More preferably, one is F and the other is CF3. In addition, in the general formula (4), -R a -(CZ 1 Z 2 ) k - is the following formula (t2): -(C=O) h -(O) i-CF2-O-(CX 7 2) e -(O) g -CZ 1 Z 2 - (t2) (In the formula, X 7 are each independently H, F, or CF3, e is an integer of 0 to 3, g is 0 or 1, h is 0 or 1, i is 0 or 1, and Z 1 and Z 2 are each independently F or CF3), and in formula (t2), Z 1 and Z 2 More preferably, one is F and the other is CF3.

[0450] The compound represented by the general formula (4) is a hydrophilic group (Y 3 ), it is also preferable that the compound has a C—F bond and does not have a C—H bond. i , X j , and X k All of the are F and R a is preferably a perfluoroalkylene group having one or more carbon atoms, and the perfluoroalkylene group may be either linear or branched, may be cyclic or acyclic, and may contain at least one catenary heteroatom. The number of carbon atoms in the perfluoroalkylene group may be 2 to 20, or may be 4 to 18.

[0451] The compound represented by the general formula (4) may be partially fluorinated. That is, the compound represented by the general formula (4) may have a hydrophilic group (Y 3 ), it is also preferred that the alkyl group has at least one hydrogen atom bonded to a carbon atom and at least one fluorine atom bonded to a carbon atom.

[0452] The compound represented by general formula (4) is also preferably a compound represented by the following formula (4a). CF2=CF-O-Rf 0 -Y 3 (4a) (In the formula, Y3 is a hydrophilic group, and Rf 0 is a perfluorinated divalent linking group which may be linear or branched, cyclic or acyclic in structure, saturated or unsaturated, substituted or unsubstituted, and which optionally contains one or more heteroatoms selected from the group consisting of sulfur, oxygen, and nitrogen.

[0453] The compound represented by general formula (4) is also preferably a compound represented by the following formula (4b). CH2=CH-O-Rf 0 -Y 3 (4b) (In the formula, Y 3 is a hydrophilic group, and Rf 0 is a perfluorinated divalent linking group defined by formula (4a).

[0454] In general formula (4), Y 3 One of the preferred embodiments is -OSO3M. 3 is -OSO3M, examples of the compound represented by general formula (4) include CF2=CF(OCF2CF2CH2OSO3M), CF2=CF(O(CF2)4CH2OSO3M), CF2=CF(OCF2CF(CF3)CH2OSO3M), CF2=CF(OCF2CF(CF3)OCF2CF2CH2OSO3M), CH2=CH((CF2)4CH2OSO3M), CF2=CF(OCF2CF2SON(CH3)CH2CH2OSO3M), CH2=CH(CF2CF2CH2OSO3M), CF2=CF(OCF2CF2CF2SON(CH3)CH2CH2OSO3M), etc. In the above formulas, M is the same as above.

[0455] In general formula (4), Y 3 Another preferred form is -SO3M. 3is -SO3M, examples of the compound represented by general formula (4) include CF2=CF(OCF2CF2SO3M), CF2=CF(O(CF2)4SO3M), CF2=CF(OCF2CF(CF3)SO3M), CF2=CF(OCF2CF(CF3)OCF2CF2SO3M), CH2=CH(CF2CF2SO3M), CF2=CF(OCF2CF(CF3)OCF2CF2CF2CF2SO3M), CH2=CH((CF2)4SO3M), CH2=CH((CF2)3SO3M), etc. In the above formulas, M is the same as above.

[0456] In general formula (4), Y 3 -COOM is also a preferred form. 3 is -COOM, the compounds represented by general formula (4) include CF2=CF(OCF2CF2COOM), CF2=CF(OCF2CF2CF2COOM), CF2=CF(O(CF2)5COOM), CF2=CF(OCF2CF(CF3)COOM), CF2=CF(OCF2CF(CF3)O(CF2) n COOM) (n is greater than 1), CH2=CH(CF2CF2COOM), CH2=CH((CF2)4COOM), CH2=CH((CF2)3COOM), CF2=CF(OCF2CF2SO2NR'CH2COOM), CF2=CF(O(CF2)4SO2NR'CH2COOM), CF2=CF(OCF2CF(CF3)SO2NR'CH2COOM), CF2=CF(OCF2CF(CF3)OCF2CF2SO2NR'CH2COOM), CH2=CH(CF2CF2SO2NR'CH2COOM), CF2=CF(OCF2CF(CF3)OCF2CF2CF2CF2SO2NR'CH2COOM), CH2=CH((CF2)4SO2NR'CH2COOM), CH2=CH((CF2)3SO2NR'CH2COOM). In the above formula, R' is H or C 1-4 is an alkyl group, and M is the same as above.

[0457] In general formula (4), Y 3 In another preferred embodiment, Y is -OPO3M or -OP(O)(OM)2.3 is -OPO3M or -OP(O)(OM)2, examples of the compound represented by general formula (4) include CF2=CF(OCF2CF2CH2OP(O)(OM)2), CF2=CF(O(CF2)4CH2OP(O)(OM)2), CF2=CF(OCF2CF(CF3)CH2OP(O)(OM)2), CF2=CF(OCF2CF(CF3)OCF2CF2CH2OP(O)(OM)2), CF2=CF(O CF2CF2SO2N(CH3)CH2CH2OP(O)(OM)2), CF2=CF(OCF2CF2CF2CF2SO2N(CH3)CH2CH2OP(O)(OM)2), CH2=CH(CF2CF2CH2OP(O)(OM)2, CH2=CH((CF2)4CH2OP(O)(OM)2), CH2=CH((CF2)3CH2OP(O)(OM)2), etc. In the above formula, M is the same as above.

[0458] In general formula (4), Y 3 In another preferred embodiment, Y is -PO3M or -P(O)(OM)2. 3 is -PO3M or -P(O)(OM)2, examples of the compound represented by general formula (4) include CF2=CF(OCF2CF2P(O)(OM)2), CF2=CF(O(CF2)4P(O)(OM)2), CF2=CF(OCF2CF(CF3)P(O)(OM)2), CF2=CF(OCF2CF(CF3)OCF2CF2P(O)(OM)2), CH2=CH(CF2CF2P(O)(OM)2), CH2=CH((CF2)4P(O)(OM)2), CH2=CH((CF2)3P(O)(OM)2), and the like, where M is the same as above.

[0459] The compound represented by general formula (4) includes compounds represented by general formula (5): CX2=CY(-CZ2-O-Rf-Y 3 ) (5) (In the formula, X's may be the same or different and each represent -H or -F; Y's may be -H, -F, an alkyl group or a fluorine-containing alkyl group; and Z's may be the same or different and each represent -H, -F, an alkyl group or a fluorine-containing alkyl group. Rf's may be a fluorine-containing alkylene group having 1 to 40 carbon atoms or a fluorine-containing alkylene group having 2 to 100 carbon atoms and an ether bond. Y 3 is the same as above.), a compound represented by general formula (6): CX2=CY(-O-Rf-Y 3 ) (6) (In the formula, X may be the same or different and is -H or -F; Y is -H, -F, an alkyl group or a fluorine-containing alkyl group; and Rf is a fluorine-containing alkylene group having 1 to 40 carbon atoms or a fluorine-containing alkylene group having 2 to 100 carbon atoms and an ether bond. Y 3 is the same as above.) and a compound represented by general formula (7): CX2=CY(-Rf-Y 3 ) (7) (In the formula, X may be the same or different and is -H or -F; Y is -H, -F, an alkyl group or a fluorine-containing alkyl group; and Rf is a fluorine-containing alkylene group having 1 to 40 carbon atoms or a fluorine-containing alkylene group having 2 to 100 carbon atoms and an ether bond. Y 3 is the same as above. Preferably, the compound is at least one selected from the group consisting of compounds represented by The fluorine-containing alkylene group having 2 to 100 carbon atoms and an ether bond is an alkylene group that does not contain a structure in which an oxygen atom is at the terminal and that contains an ether bond between carbon atoms.

[0460] In general formula (5), X is -H or -F. Both Xs may be -F, or at least one X may be -H. For example, one X may be -F and the other may be -H, or both Xs may be -H.

[0461] In the general formula (5), Y is —H, —F, an alkyl group or a fluorine-containing alkyl group. The alkyl group is an alkyl group that does not contain a fluorine atom, and may have a carbon number of at least 1. The alkyl group preferably has 6 or less carbon atoms, more preferably 4 or less carbon atoms, and even more preferably 3 or less carbon atoms. The fluorine-containing alkyl group is an alkyl group containing at least one fluorine atom, and may have a carbon number of at least 1. The fluorine-containing alkyl group preferably has 6 or less carbon atoms, more preferably 4 or less carbon atoms, and even more preferably 3 or less carbon atoms. The above Y is preferably -H, -F or -CF3, and more preferably -F.

[0462] In general formula (5), Z may be the same or different and is —H, —F, an alkyl group or a fluoroalkyl group. The alkyl group is an alkyl group that does not contain a fluorine atom, and may have a carbon number of at least 1. The alkyl group preferably has 6 or less carbon atoms, more preferably 4 or less carbon atoms, and even more preferably 3 or less carbon atoms. The fluorine-containing alkyl group is an alkyl group containing at least one fluorine atom, and may have a carbon number of at least 1. The fluorine-containing alkyl group preferably has 6 or less carbon atoms, more preferably 4 or less carbon atoms, and even more preferably 3 or less carbon atoms. The above Z is preferably -H, -F or -CF3, and more preferably -F.

[0463] In general formula (5), it is preferable that at least one of X, Y, and Z contains a fluorine atom. For example, X may be —H, and Y and Z may be —F.

[0464] In the general formula (5), Rf is a fluorine-containing alkylene group having 1 to 40 carbon atoms or a fluorine-containing alkylene group having 2 to 100 carbon atoms and an ether bond. The number of carbon atoms in the fluorine-containing alkylene group is preferably 2 or more. Also, it is preferably 30 or less, more preferably 20 or less, and even more preferably 10 or less. Examples of the fluorine-containing alkylene group include -CF2-, -CH2CF2-, -CF2CF2-, -CF2CH2-, -CF2CF2CH2-, -CF(CF3)-, -CF(CF3)CF2-, and -CF(CF3)CH2-. The fluorine-containing alkylene group is preferably a perfluoroalkylene group.

[0465] The number of carbon atoms in the fluorine-containing alkylene group having an ether bond is preferably 3 or more. The number of carbon atoms in the fluorine-containing alkylene group having an ether bond is preferably 60 or less, more preferably 30 or less, and even more preferably 12 or less. Examples of the fluorine-containing alkylene group having an ether bond include those represented by the following formula: [ka] (In the formula, Z 1 is F or CF3;Z 2 and Z 3 are H or F;Z respectively 4 is also preferably a divalent group represented by the formula: H, F, or CF3; p1+q1+r1 is an integer of 1 to 10; s1 is 0 or 1; and t1 is an integer of 0 to 5). Specific examples of the fluorine-containing alkylene group having an ether bond include -CF(CF3)CF2-O-CF(CF3)-, -(CF(CF3)CF2-O) n -CF(CF3)- (wherein n is an integer of 1 to 10), -CF(CF3)CF2-O-CF(CF3)CH2-, -(CF(CF3)CF2-O) n Examples include -CF(CF3)CH2- (wherein n is an integer of 1 to 10), -CH2CF2CF2O-CH2CF2CH2-, -CF2CF2CF2O-CF2CF2-, -CF2CF2CF2O-CF2CF2CH2-, -CF2CF2O-CF2-, -CF2CF2O-CF2CH2-, etc. The fluorine-containing alkylene group having an ether bond is preferably a perfluoroalkylene group.

[0466] In the general formula (5), Y3 is -COOM, -SO3M or -OSO3M (M is H, a metal atom, NR 7y 4. An imidazolium which may have a substituent, a pyridinium which may have a substituent, or a phosphonium which may have a substituent, R 7y are H or organic groups and may be the same or different. Any two of them may be bonded to each other to form a ring. R 7y The organic group in is preferably an alkyl group. R 7y As for H or C 1-10 is preferably an organic group represented by the formula: 1-4 The organic group is more preferably H or C 1-4 More preferred are alkyl groups of the formula: The metal atom includes alkali metals (Group 1) and alkaline earth metals (Group 2), and is preferably Na, K or Li. M is -H, a metal atom, or NR 7 4 is preferred, and -H, an alkali metal (Group 1), an alkaline earth metal (Group 2) or NR 7 4 is more preferred, -H, -Na, -K, -Li or NH4 is even more preferred, -H, -Na, -K or NH4 is even more preferred, -H, -Na or NH4 is especially preferred, and -H or -NH4 is most preferred. Above Y 3 As the alkyl group, -COOM or -SO3M is preferred, and -COOM is more preferred.

[0467] The compound represented by general formula (5) is preferably a compound (5a) represented by general formula (5a). CH2=CF(-CF2-O-Rf-Y 3 ) (5a) (Wherein Rf and Y 3 is the same as above.)

[0468] Specific examples of the compound represented by the general formula (5a) include compounds represented by the following formula:

[0469] [ka]

[0470] (In the formula, Z 1 is F or CF3;Z 2 and Z 3 are H or F;Z respectively 4 is H, F, or CF3; p1+q1+r1 are integers between 0 and 10; s1 is 0 or 1; t1 is an integer between 0 and 5; Y 3 is the same as above, except for Z 3 and Z 4 are both H, then p1+q1+r1+s1 is not 0). More specifically, compounds represented by the following formula are included:

[0471] [ka]

[0472] Among them,

[0473] [ka]

[0474] It is preferable that:

[0475] The compound represented by general formula (5a) includes compounds represented by formula (5a) 3 is preferably -COOM, and particularly preferably at least one selected from the group consisting of CH2=CFCF2OCF(CF3)COOM and CH2=CFCF2OCF(CF3)CF2OCF(CF3)COOM (wherein M is as defined above), and more preferably CH2=CFCF2OCF(CF3)COOM.

[0476] The compound represented by general formula (5) is preferably a compound (5b) represented by general formula (5b). CX 2 2=CFCF2-O-(CF(CF3)CF2O) n5 -CF(CF3)-Y 3 (5b) (In the formula, each 2 are the same and represent F or H. n5 represents 0 or an integer of 1 to 10, and Y 3 is the same as the definition above.)

[0477] In the formula (5b), n5 is preferably 0 or an integer of 1 to 5, more preferably 0, 1 or 2, and even more preferably 0 or 1, from the viewpoint of the stability of the resulting aqueous dispersion. 3 is preferably -COOM in that it provides adequate water solubility and stability of the aqueous dispersion, and the above M is preferably H or NH4 in that it is less likely to remain as an impurity and the heat resistance of the obtained molded body is improved.

[0478] Examples of the compound represented by the above formula (5b) include CH2=CFCF2OCF(CF3)COOM and CH2=CFCF2OCF(CF3)CF2OCF(CF3)COOM (wherein M is as defined above).

[0479] Further, examples of the compound represented by general formula (5) include a compound represented by general formula (5c).

[0480] CF2=CFCF2-O-Rf-Y 3 (5c) (Wherein Rf and Y 3 is the same as above)

[0481] More specifically, [ka] etc.

[0482] In general formula (6), X is -H or -F. Both Xs may be -F, or at least one X may be -H. For example, one X may be -F and the other may be -H, or both Xs may be -H.

[0483] In the general formula (6), Y is —H, —F, an alkyl group or a fluorine-containing alkyl group. The alkyl group is an alkyl group that does not contain a fluorine atom, and may have a carbon number of at least 1. The alkyl group preferably has 6 or less carbon atoms, more preferably 4 or less carbon atoms, and even more preferably 3 or less carbon atoms. The fluorine-containing alkyl group is an alkyl group containing at least one fluorine atom, and may have a carbon number of at least 1. The fluorine-containing alkyl group preferably has 6 or less carbon atoms, more preferably 4 or less carbon atoms, and even more preferably 3 or less carbon atoms. The above Y is preferably -H, -F or -CF3, and more preferably -F.

[0484] In general formula (6), it is preferable that at least one of X and Y contains a fluorine atom. For example, X may be —H, and Y and Z may be —F.

[0485] In the general formula (6), Rf is a fluorine-containing alkylene group having 1 to 40 carbon atoms or a fluorine-containing alkylene group having 2 to 100 carbon atoms and an ether bond. The number of carbon atoms in the fluorine-containing alkylene group is preferably 2 or more. The number of carbon atoms in the fluorine-containing alkylene group is preferably 30 or less, more preferably 20 or less, and even more preferably 10 or less. Examples of the fluorine-containing alkylene group include -CF2-, -CH2CF2-, -CF2CF2-, -CF2CH2-, -CF2CF2CH2-, -CF(CF3)-, -CF(CF3)CF2-, and -CF(CF3)CH2-. The fluorine-containing alkylene group is preferably a perfluoroalkylene group.

[0486] In the above general formula (6), Y 3 is -COOM, -SO3M or -OSO3M (M is H, a metal atom, NR 7y 4. An imidazolium which may have a substituent, a pyridinium which may have a substituent, or a phosphonium which may have a substituent, R 7yare H or organic groups and may be the same or different. Any two of them may be bonded to each other to form a ring. R 7y The organic group in R is preferably an alkyl group. 7y As for H or C 1-10 is preferably an organic group represented by the formula: 1-4 The organic group is more preferably H or C 1-4 More preferred are alkyl groups of the formula: The metal atom includes alkali metals (Group 1) and alkaline earth metals (Group 2), and is preferably Na, K or Li. M is -H, a metal atom, or NR 7 4 is preferred, and -H, an alkali metal (Group 1), an alkaline earth metal (Group 2) or NR 7 4 is more preferred, -H, -Na, -K, -Li or NH4 is even more preferred, -H, -Na, -K or NH4 is even more preferred, -H, -Na or NH4 is especially preferred, and -H or -NH4 is most preferred. Above Y 3 As the alkyl group, -COOM or -SO3M is preferred, and -COOM is more preferred.

[0487] The compound represented by general formula (6) is preferably at least one selected from the group consisting of compounds represented by general formulae (6a), (6b), (6c), (6d) and (6e). CF2=CF-O-(CF2) n1 -Y 3 (6a) (wherein n1 represents an integer of 1 to 10, and Y 3 is the same as the definition above.) CF2=CF-O-(CF2C(CF3)F) n2 -Y 3 (6b) (wherein n2 represents an integer of 1 to 5, and Y 3 is the same as the definition above.) CF2=CF-O-(CFX 1 ) n3 -Y 3 (6c) (In the formula, X 1represents F or CF3, n3 represents an integer of 1 to 10, and Y 3 is the same as the definition above.) CF2=CF-O-(CF2CFX 1 O) n4 -(CF2) n6 -Y 3 (6d) (wherein n4 represents an integer of 1 to 10, n6 represents an integer of 1 to 3, and Y 3 and X 1 is the same as the definition above.) CF2=CF-O-(CF2CF2CFX 1 O) n5 -CF2CF2CF2-Y 3 (6e) (wherein n5 represents an integer of 0 to 10, and Y 3 and X 1 is the same as the definition above.)

[0488] In the formula (6a), n1 is preferably an integer of 5 or less, and more preferably an integer of 2 or less. 3 is preferably -COOM in that it provides suitable water solubility and stability of the aqueous dispersion, and M is preferably H or NH4 in that it is less likely to remain as an impurity and the heat resistance of the resulting molded article is improved.

[0489] Examples of the compound represented by the above formula (6a) include CF2=CF-O-CF2COOM, CF2=CF(OCF2CF2COOM), and CF2=CF(OCF2CF2CF2COOM) (wherein M is as defined above).

[0490] In the formula (6b), n2 is preferably an integer of 3 or less in terms of the stability of the resulting aqueous dispersion, and Y 3 is preferably -COOM in that it provides suitable water solubility and stability of the aqueous dispersion, and M is preferably H or NH4 in that it is less likely to remain as an impurity and the heat resistance of the resulting molded article is improved.

[0491] In the formula (6c), n3 is preferably an integer of 5 or less in terms of water solubility, and Y 3 is preferably -COOM in that it provides suitable water solubility and stability of the aqueous dispersion, and the above M is preferably H or NH4 in that it provides good dispersion stability.

[0492] In the above formula (6d), the above X 1 is preferably —CF3 from the viewpoint of stability of the aqueous dispersion, n4 is preferably an integer of 5 or less from the viewpoint of water solubility, and Y 3 is preferably -COOM in that it provides adequate water solubility and stability of the aqueous dispersion, and the above M is preferably H or NH4.

[0493] Examples of the compound represented by the above formula (6d) include CF2=CFOCF2CF(CF3)OCF2CF2COOM, CF2=CFOCF2CF(CF3)OCF2COOM, and CF2=CFOCF2CF(CF3)OCF2CF2CF2COOM (wherein M represents H, NH4, or an alkali metal).

[0494] In the general formula (6e), n5 is preferably an integer of 5 or less in terms of water solubility, and Y 3 is preferably -COOM in that it provides adequate water solubility and stability of the aqueous dispersion, and the above M is preferably H or NH4.

[0495] An example of the compound represented by general formula (6e) is CF2=CFOCF2CF2CF2COOM (wherein M represents H, NH4 or an alkali metal).

[0496] In general formula (7), Rf is preferably a fluorine-containing alkylene group having a carbon number of 1 to 40. In general formula (7), at least one of X and Y preferably contains a fluorine atom.

[0497] The compound represented by general formula (7) is represented by general formula (7a): CF2=CF-(CF2) n1 -Y 3 (7a) (wherein n1 represents an integer of 1 to 10, and Y 3 is as defined above.) and a compound represented by general formula (7b): CF2=CF-(CF2C(CF3)F) n2 -Y 3 (7b) (wherein n2 represents an integer of 1 to 5, and Y 3 is as defined above. Preferably, at least one compound selected from the group consisting of compounds represented by Above Y 3 is preferably -SO3M or -COOM, and M is H, a metal atom, NR 7y 4. It is preferably an imidazolium which may have a substituent, a pyridinium which may have a substituent, or a phosphonium which may have a substituent. 7y represents H or an organic group.

[0498] In the formula (7a), n1 is preferably an integer of 5 or less, and more preferably an integer of 2 or less. 3 is preferably -COOM in that it provides suitable water solubility and stability of the aqueous dispersion, and M is preferably H or NH4 in that it is less likely to remain as an impurity and the heat resistance of the resulting molded article is improved. An example of the compound represented by the above formula (7a) is CF2=CFCF2COOM (wherein M is as defined above).

[0499] In the formula (7b), n2 is preferably an integer of 3 or less in terms of the stability of the resulting aqueous dispersion, and Y 3 is preferably -COOM in that it provides suitable water solubility and stability of the aqueous dispersion, and M is preferably H or NH4 in that it is less likely to remain as an impurity and the heat resistance of the resulting molded article is improved.

[0500] The above-mentioned modified monomer preferably contains modified monomer (A), and preferably contains at least one selected from the group consisting of compounds represented by general formula (5a), general formula (5c), general formula (6a), general formula (6b), general formula (6c), and general formula (6d), and more preferably contains a compound represented by general formula (5a) or general formula (5c).

[0501] When the modifying monomer (A) is used as the modifying monomer, the content of the modifying monomer (A) units is preferably in the range of 0.00001 to 1.0% by mass relative to the total polymerized units of the TFE polymer (PTFE). The lower limit is more preferably 0.0001% by mass, more preferably 0.0005% by mass, even more preferably 0.001% by mass, and even more preferably 0.005% by mass. The upper limit is, in order of preference, 0.90%, 0.50%, 0.40%, 0.30%, 0.20%, 0.15%, 0.10%, 0.08%, 0.05%, and 0.01% by mass.

[0502] In producing the TFE polymer, polymer (I) can be used within the range of use in the production method of the present disclosure described above. The concentration of polymer (I) is not particularly limited as long as it is within the above range. If the amount added is too large, acicular particles with a large aspect ratio are formed, the aqueous dispersion becomes gel-like, and stability is impaired. The lower limit of the amount of polymer (I) used is preferably 0.0001% by mass, more preferably 0.001% by mass, even more preferably 0.01% by mass, and particularly preferably 0.02% by mass, relative to the aqueous medium. The upper limit of the amount of polymer (I) used is preferably 10% by mass, more preferably 5% by mass, relative to the aqueous medium.

[0503] The polymer (I) may be added to a reaction vessel all at once before the start of polymerization, or all at once after the start of polymerization, or may be added in multiple divided portions during polymerization, or may be added continuously during polymerization.

[0504] In the production of the TFE polymer, persulfates (e.g., ammonium persulfate) and organic peroxides such as disuccinic acid peroxide and diglutaric acid peroxide can be used as polymerization initiators, either alone or in the form of a mixture thereof. They may also be used in combination with a reducing agent such as sodium sulfite to form a redox system. Furthermore, during polymerization, a radical scavenger such as hydroquinone or catechol, or a peroxide decomposer such as ammonium sulfite, can be added to adjust the radical concentration in the system.

[0505] As the redox polymerization initiator, it is preferable to use a redox initiator that combines an oxidizing agent and a reducing agent. Examples of oxidizing agents include persulfates, organic peroxides, potassium permanganate, manganese triacetate, and cerium ammonium nitrate. Examples of reducing agents include sulfites, bisulfites, bromates, diimines, and oxalic acid. Examples of persulfates include ammonium persulfate and potassium persulfate. Examples of sulfites include sodium sulfite and ammonium sulfite. To increase the decomposition rate of the initiator, it is also preferable to add a copper salt or an iron salt to the combination of redox initiators. Examples of copper salts include copper(II) sulfate, and examples of iron salts include iron(II) sulfate.

[0506] Examples of the redox initiator include potassium permanganate / oxalic acid, ammonium persulfate / bisulfite / iron sulfate, manganese triacetate / oxalic acid, cerium ammonium nitrate / oxalic acid, and bromate / bisulfite, with potassium permanganate / oxalic acid being preferred. When using a redox initiator, either an oxidizing agent or a reducing agent may be charged into a polymerization vessel in advance, and then the other may be added continuously or intermittently to initiate polymerization. For example, when potassium permanganate / oxalic acid is used, it is preferred to charge oxalic acid into a polymerization vessel and then continuously add potassium permanganate thereto.

[0507] In the production of the TFE polymer, known chain transfer agents can be used, including, for example, saturated hydrocarbons such as methane, ethane, propane, and butane; halogenated hydrocarbons such as chloromethane, dichloromethane, and difluoroethane; alcohols such as methanol, ethanol, and isopropanol; and hydrogen. However, those that are in a gaseous state at room temperature and normal pressure are preferred.

[0508] The amount of the chain transfer agent used is usually 1 to 10,000 ppm by mass, and preferably 1 to 5,000 ppm by mass, based on the total amount of TFE supplied.

[0509] In the production of the TFE polymer, a saturated hydrocarbon having 12 or more carbon atoms that is substantially inert to the reaction and becomes liquid under the reaction conditions can also be used as a dispersion stabilizer for the reaction system in an amount of 2 to 10 parts by mass per 100 parts by mass of the aqueous medium. Furthermore, ammonium carbonate, ammonium phosphate, or the like can be added as a buffer to adjust the pH during the reaction.

[0510] When the polymerization of TFE is completed, a polymer dispersion having a solid content of 1.0 to 70 mass % and an average primary particle size of 50 to 500 nm can be obtained. The lower limit of the solid content is preferably 5% by mass, more preferably 8% by mass, and the upper limit is not particularly limited, but may be 40% by mass or 35% by mass. The lower limit of the average primary particle size is preferably 100 nm, more preferably 150 nm, and the upper limit is preferably 400 nm, more preferably 350 nm. The average primary particle size can be measured by dynamic light scattering. An aqueous dispersion adjusted to a solids concentration of approximately 1.0% by mass is prepared, and the average primary particle size is measured by dynamic light scattering at 25°C, with a refractive index of 1.3328 and a viscosity of 0.8878 mPa·s for the solvent (water), and 70 cumulative measurements. For example, an ELSZ-1000S (manufactured by Otsuka Electronics Co., Ltd.) can be used for the dynamic light scattering method.

[0511] Fine powders can be produced by coagulating aqueous dispersions of TFE polymers. The aqueous dispersions of TFE polymers can be used for various applications as fine powders after coagulation, washing, and drying. When coagulating the aqueous dispersions of TFE polymers, the aqueous dispersion obtained by polymerization of a polymer latex or the like is typically diluted with water to a polymer concentration of 5 to 20% by mass. In some cases, the pH is adjusted to neutral or alkaline, and the mixture is stirred in a vessel equipped with a stirrer with more vigor than during the reaction. The coagulation may be performed while stirring, using a coagulant such as a water-soluble organic compound (e.g., methanol or acetone), an inorganic salt (e.g., potassium nitrate or ammonium carbonate), or an inorganic acid (e.g., hydrochloric acid, sulfuric acid, or nitric acid). The coagulation may also be performed continuously using an in-line mixer or the like.

[0512] The concentration of the unaggregated TFE polymer in the wastewater resulting from the aggregation is preferably low from the viewpoint of productivity, more preferably less than 0.4% by mass, and particularly preferably less than 0.3% by mass.

[0513] By adding pigments for coloring or various fillers for improving mechanical properties before or during the coagulation, it is possible to obtain a pigmented or filled TFE polymer fine powder in which the pigments and fillers are uniformly mixed.

[0514] The wet powder obtained by coagulating the aqueous dispersion of the TFE polymer is usually dried by means of vacuum, high frequency, hot air, or the like, while keeping the wet powder in a state where it is not fluidized much, preferably in a static state. Friction between powders, particularly at high temperatures, generally has an undesirable effect on fine powder-type TFE polymers. This is because particles made of this type of TFE polymer tend to easily fibrillate even with a small shear force, losing their original stable particle structure.

[0515] The drying is carried out at a drying temperature of 10 to 300°C, preferably 100 to 300°C.

[0516] In the manufacturing method of the present disclosure, a high-purity fluoropolymer-containing composition is obtained by subjecting a composition such as the TFE polymer fine powder obtained in this manner to fluorine radical treatment. The resulting high-purity fluoropolymer-containing composition is less likely to generate gas during molding and is less likely to lose weight when heated. Therefore, by molding the resulting high-purity fluoropolymer-containing composition, molded articles with almost no cracks and beautiful surfaces can be obtained. Furthermore, high-purity fluoropolymer-containing compositions such as fluorine radical-treated TFE polymer fine powder can be stably extruded during paste extrusion molding, giving molded articles with excellent surface smoothness and dimensional stability.

[0517] The resulting TFE polymer fine powder is suitable for molding, and suitable applications include tubes for hydraulic and fuel systems in aircraft and automobiles, flexible hoses for chemical solutions, steam, etc., and for electrical wire coating.

[0518] The aqueous dispersion of the TFE polymer can also be stabilized and further concentrated by adding a nonionic surfactant, and used in various applications as a composition to which an organic or inorganic filler is added depending on the purpose. By coating the composition on a substrate made of metal or ceramic, it is possible to form a coating surface that has non-adhesiveness and a low coefficient of friction, and is excellent in gloss, smoothness, abrasion resistance, weather resistance, and heat resistance, and is suitable for painting rolls, cooking utensils, etc., and for impregnating glass cloth.

[0519] An organosol of a TFE polymer can also be prepared from the aqueous dispersion. The organosol can contain the TFE polymer and an organic solvent. Examples of the organic solvent include ether solvents, ketone solvents, alcohol solvents, amide solvents, ester solvents, aliphatic hydrocarbon solvents, aromatic hydrocarbon solvents, and halogenated hydrocarbon solvents. N-methyl-2-pyrrolidone, dimethylacetamide, and the like are preferably used. The organosol can be prepared, for example, by the method described in International Publication No. 2012 / 002038.

[0520] The aqueous dispersion of the TFE polymer or the fine powder of the TFE polymer is also preferably used as a processing aid. When used as a processing aid, the aqueous dispersion or the fine powder is mixed with a host polymer or the like to improve the melt strength during melt processing of the host polymer, and the mechanical strength, electrical properties, flame retardancy, anti-dripping property during combustion, and sliding properties of the resulting polymer.

[0521] The above-mentioned aqueous dispersion of the TFE polymer or the above-mentioned TFE polymer fine powder is also preferably used as a binder for batteries and for dust prevention purposes.

[0522] The aqueous dispersion of the TFE polymer or the fine powder of the TFE polymer may also be preferably used as a processing aid after being compounded with a resin other than the TFE polymer. The aqueous dispersion or the fine powder is suitable as a raw material for PTFE, as described in, for example, JP-A-11-49912, U.S. Pat. No. 5,804,654, JP-A-11-29679, and JP-A-2003-2980. Processing aids using the aqueous dispersion or the fine powder are in no way inferior to the processing aids described in the above publications.

[0523] The aqueous dispersion of above-mentioned TFE polymer can also be mixed with the aqueous dispersion of melt-processable fluororesin to be coagulated, and be made into coprecipitated powder.Above-mentioned coprecipitated powder is suitable as processing aid.

[0524] Examples of the melt-processable fluororesin include FEP, PFA, TFE / perfluoroallyl ether copolymer, ethylene / TFE copolymer [ETFE], and ethylene / TFE / HFP copolymer [EFEP]. Of these, FEP, PFA, or TFE / perfluoroallyl ether copolymer is preferred.

[0525] The aqueous dispersion preferably contains the melt-processable fluororesin. Examples of the melt-processable fluororesin include FEP, PFA, TFE / perfluoroallyl ether copolymer, ETFE, and EFEP. The aqueous dispersion containing the melt-processable fluororesin can be used as a coating material. The melt-processable fluororesin can sufficiently fuse the TFE polymer particles together, improving film-forming properties and imparting gloss to the resulting coating.

[0526] The fluorine-free resin that adds above-mentioned coprecipitated powder can be powder, can be pellet, can be emulsion.In order to thoroughly mix each resin, it is preferable to add above-mentioned by known method such as extrusion kneading, roll kneading, etc., while applying shearing force.

[0527] The aqueous dispersion of the TFE polymer is also preferably used as a dust-suppressing treatment. The dust-suppressing treatment can be used in a method of mixing the TFE polymer with a dust-generating substance and subjecting the mixture to a compression-shear action at a temperature of 20 to 200°C to fibrillate the TFE polymer and suppress dust from the dust-generating substance, such as the methods described in Japanese Patent No. 2827152 and Japanese Patent No. 2538783. The aqueous dispersion of the TFE polymer can be suitably used, for example, in the dust suppression treatment composition described in WO 2007 / 004250, and can also be suitably used in the dust suppression treatment method described in WO 2007 / 000812.

[0528] The dust suppression treatment agent is suitable for use in the fields of building materials, soil stabilization materials, solidification materials, fertilizers, landfill disposal of incineration ash and hazardous substances, explosion prevention, cosmetics, and dust suppression treatment of sand for pet excretion, such as cat litter.

[0529] The aqueous dispersion of the TFE polymer is also preferably used as a raw material for obtaining TFE polymer fibers by the dispersion spinning method, which is a method in which the aqueous dispersion of the TFE polymer and an aqueous dispersion of a matrix polymer are mixed, the mixture is extruded to form an intermediate fiber structure, and the intermediate fiber structure is fired to decompose the matrix polymer and sinter the TFE polymer particles, thereby obtaining TFE polymer fibers.

[0530] High molecular weight PTFE powder has extensibility and non-melt processability, and is also useful as a raw material for extruded bodies (porous bodies). When this stretched body is a membrane (a stretched PTFE membrane or a porous PTFE membrane), it can be stretched by a known PTFE stretching method. By stretching, the high-molecular-weight PTFE is easily fibrillated, forming a porous PTFE body (membrane) consisting of nodes and fibers. Preferably, a sheet-like or rod-like paste extrudate is roll-stretched in the extrusion direction to obtain a uniaxially stretched film. Furthermore, a biaxially stretched film can also be obtained by stretching the film in the width direction using a tenter or the like. It is also preferable to carry out a semi-baking treatment before stretching.

[0531] This expanded PTFE body is a porous body with high porosity and can be suitably used as a filter medium for various precision filters such as air filters and chemical filters, a support material for polymer electrolyte membranes, and the like. It is also useful as a material for products used in the fields of textiles, medicine, electrochemicals, sealing materials, air filtration, ventilation / internal pressure adjustment, liquid filtration, and general consumer goods. Specific examples of applications are given below.

[0532] Electrochemical field Dielectric material prepreg, EMI shielding material, heat transfer material, etc. More specifically, printed wiring boards, electromagnetic shielding materials, insulating heat transfer materials, insulating materials, etc. Sealing materials field Gaskets, packing, pump diaphragms, pump tubes, aircraft sealing materials, etc.

[0533] Air Filtration ULPA filters (for semiconductor manufacturing), HEPA filters (for hospitals and semiconductor manufacturing), cylindrical cartridge filters (for industrial use), bag filters (for industrial use), heat-resistant bag filters (for exhaust gas treatment), heat-resistant pleated filters (for exhaust gas treatment), SINBRAN filters (for industrial use), catalytic filters (for exhaust gas treatment), adsorbent filters (for HDD integration), adsorbent vent filters (for HDD integration), vent filters (for HDD integration and others), vacuum cleaner filters (for vacuum cleaners), general-purpose multi-layer felt material, GT cartridge filters (for GT compatible products), cooling filters (for electronic equipment housings), etc.

[0534] Ventilation / internal pressure regulation field Freeze-drying materials such as freeze-drying containers, automotive ventilation materials for electronic circuits and lamps, container applications such as container caps, protective ventilation applications for electronic devices including small terminals such as tablet devices and mobile phones, medical ventilation applications, etc.

[0535] Liquid Filtration Semiconductor liquid filtration filters (for semiconductor manufacturing), hydrophilic PTFE filters (for semiconductor manufacturing), chemical filters (for chemical liquid treatment), filters for pure water production lines (for pure water production), backwash type liquid filtration filters (for industrial wastewater treatment), etc.

[0536] General consumer goods Clothing, cable guides (movable wires for motorcycles), motorcycle clothing, cast liners (medical supporters), vacuum cleaner filters, bagpipes (musical instruments), cables (guitar signal cables, etc.), strings (for stringed instruments), etc.

[0537] Textile field PTFE fiber (textile material), sewing thread (textile), weaving thread (textile), rope, etc.

[0538] Medical field Implants (extended products), artificial blood vessels, catheters, general surgery (tissue reinforcement materials), head and neck products (dura mater replacement), oral health (tissue regenerative medicine), orthopedics (bandages), etc.

[0539] The manufacturing method of the present disclosure also allows for the production of low molecular weight PTFE. Low-molecular-weight PTFE may be produced by polymerization, or by lowering the molecular weight of high-molecular-weight PTFE obtained by polymerization by a known method (thermal decomposition, decomposition by irradiation, etc.).

[0540] Low-molecular-weight PTFE (also called PTFE micropowder) having a molecular weight of 600,000 or less has excellent chemical stability, extremely low surface energy, and is resistant to fibrillation. Therefore, it is suitable as an additive for improving the slipperiness and texture of coating surfaces in the production of plastics, inks, cosmetics, paints, greases, office automation equipment components, toners, etc. (see, for example, JP-A-10-147617).

[0541] Furthermore, a low-molecular-weight PTFE may be obtained by dispersing a polymerization initiator and polymer (I) in an aqueous medium in the presence of a chain transfer agent, and polymerizing TFE with TFE or a monomer copolymerizable with TFE. In this case, the chain transfer agent is preferably at least one selected from the group consisting of alkanes having 2 to 4 carbon atoms. Specifically, methane, ethane, propane, butane, and isobutane are more preferred, and ethane and propane are even more preferred. In this case, the amount of chain transfer agent is preferably 10 ppm by mass or more or more than 10 ppm by mass relative to the aqueous medium.

[0542] When the low-molecular-weight PTFE obtained by the above polymerization is used as a powder, the aqueous dispersion can be coagulated to form powder particles.

[0543] In this disclosure, high molecular weight PTFE refers to non-melt-processible and fibrillating PTFE, while low molecular weight PTFE refers to melt-processible and non-fibrillating PTFE.

[0544] The term "non-melt processable" means that the melt flow rate cannot be measured at a temperature higher than the crystallization melting point in accordance with ASTM D 1238 and D 2116.

[0545] The presence or absence of fibrillating properties can be determined by "paste extrusion," a typical method for molding "high molecular weight PTFE powder," a powder made from a TFE polymer. Paste extrusion is usually possible because high molecular weight PTFE has fibrillating properties. If the unsintered molded product obtained by paste extrusion has no substantial strength or elongation, for example, if it breaks when pulled at 0% elongation, it can be considered to have no fibrillating properties.

[0546] The high-molecular-weight PTFE preferably has a standard specific gravity (SSG) of 2.130 to 2.280. The standard specific gravity is measured by a water displacement method in accordance with ASTM D 792 using a sample molded in accordance with ASTM D4895-89. In the present disclosure, "high molecular weight" means that the standard specific gravity is within the above range.

[0547] The above low molecular weight PTFE has a melt viscosity of 1×10 at 380°C. 2 ~7×10 5 The molecular weight is Pa·s. In the present disclosure, "low molecular weight" means that the melt viscosity is within the above range. The melt viscosity is measured in accordance with ASTM D 1238 using a flow tester (manufactured by Shimadzu Corporation) and a 2φ-8L die, with a 2g sample preheated to 380°C for 5 minutes, and maintained at the above temperature under a load of 0.7 MPa.

[0548] The high-molecular-weight PTFE has a melt viscosity significantly higher than that of the low-molecular-weight PTFE, making it difficult to measure its melt viscosity accurately. On the other hand, while the melt viscosity of the low-molecular-weight PTFE can be measured, it is difficult to obtain a molded article from the low-molecular-weight PTFE that can be used to measure its standard gravity, making it difficult to measure its standard gravity accurately. Therefore, in this disclosure, standard gravity is used as an indicator of the molecular weight of the high-molecular-weight PTFE, and melt viscosity is used as an indicator of the molecular weight of the low-molecular-weight PTFE. There are no known methods for directly determining the molecular weight of either the high-molecular-weight PTFE or the low-molecular-weight PTFE.

[0549] The high-molecular-weight PTFE preferably has a peak temperature of 333 to 347°C, more preferably 335 to 345°C. The low-molecular-weight PTFE preferably has a peak temperature of 322 to 333°C, more preferably 324 to 332°C. The peak temperature can be identified as the temperature corresponding to the maximum value that appears on a differential thermal analysis (DTA) curve obtained by using a TG / DTA (thermogravimetric / differential thermal analyzer) to raise the temperature of PTFE that has no history of being heated to a temperature of 300°C or higher at a rate of 10°C / min.

[0550] The peak temperature of the PTFE may be 322 to 347°C. When the PTFE is a high molecular weight PTFE, the upper limit of the peak temperature of the PTFE may be 347°C or less, 346°C or less, 345°C or less, 344°C or less, 343°C or less, 342°C or less, 341°C or less, or 340°C or less. When the PTFE is a high-molecular-weight PTFE, the lower limit of the peak temperature of the PTFE may be 333°C or higher, or 335°C or higher. When the PTFE is a low-molecular-weight PTFE, the upper limit of the peak temperature of the PTFE may be 333°C or less, or 332°C or less. When the PTFE is a low-molecular-weight PTFE, the lower limit of the peak temperature of the PTFE may be 322°C or higher, or 324°C or higher.

[0551] The average primary particle diameter of the primary particles of the low-molecular-weight PTFE is preferably 10 to 200 nm, more preferably 20 nm or more, more preferably 140 nm or less, even more preferably 150 nm or less, and particularly preferably 90 nm or less. A relatively small average primary particle diameter of the primary particles can be obtained, for example, by adding a modifying monomer to the polymerization system at the initial stage of TFE polymerization.

[0552] The average primary particle size of low-molecular-weight PTFE primary particles can be measured by dynamic light scattering. First, an aqueous dispersion of low-molecular-weight PTFE is prepared with a polymer solids concentration of approximately 1.0% by mass. Measurements can then be performed using dynamic light scattering at a measurement temperature of 25°C, a refractive index of the solvent (water) of 1.3328, a viscosity of the solvent (water) of 0.8878 mPa·s, and 70 cumulative measurements. For dynamic light scattering, an ELSZ-1000S (manufactured by Otsuka Electronics Co., Ltd.) can be used, for example.

[0553] The high-molecular-weight PTFE preferably exhibits at least one endothermic peak in the range of 333 to 347°C in a heat of fusion curve when PTFE that has not been heated to a temperature of 300°C or higher is heated at a rate of 10°C / min using a differential scanning calorimeter (DSC), and the heat of fusion between 290 and 350°C calculated from the heat of fusion curve is 52 mJ / mg or more. The heat of fusion of PTFE is more preferably 55 mJ / mg or more, and even more preferably 58 mJ / mg or more.

[0554] An unsintered tape (green tape) can also be obtained from the PTFE fine powder obtained above.

[0555] (II) Melt-processable fluororesin (1) In the production method of the present disclosure, the polymerization of FEP is preferably carried out at a polymerization temperature of 10 to 150° C. and a polymerization pressure of 0.3 to 6.0 MPaG.

[0556] The monomer composition (mass %) of FEP is preferably TFE:HFP=(60-95):(5-40), more preferably (85-92):(8-15).

[0557] In addition to TFE and HFP, other monomers copolymerizable with these monomers may be polymerized to obtain a copolymer of TFE, HFP, and other monomers as FEP. Examples of the other monomers include the above-mentioned fluorine-containing monomers (excluding TFE and HFP) and non-fluorine-containing monomers. One or more types of other monomers may be used. Perfluoro(alkyl vinyl ether) is preferred as the other monomer. The content of the other monomer units in FEP may be 0.1 to 2% by mass based on the total monomer units.

[0558] In the polymerization of the FEP, the polymer (I) can be used within the range of use in the production method of the present disclosure, but is usually added in an amount of 0.0001 to 10% by mass relative to 100% by mass of the aqueous medium.

[0559] In the polymerization of FEP, it is preferable to use cyclohexane, methanol, ethanol, propanol, ethane, propane, butane, pentane, hexane, carbon tetrachloride, chloroform, methylene chloride, methyl chloride, or the like as a chain transfer agent, and it is preferable to use ammonium carbonate, disodium hydrogen phosphate, or the like as a pH buffer.

[0560] The aqueous dispersion of FEP obtained by the manufacturing method of the present disclosure may be subjected to post-treatment such as concentration as necessary, dried, powdered, and then melt-extruded into pellets. The aqueous medium in the aqueous dispersion of FEP may contain additives such as a nonionic surfactant as necessary, and may also contain a water-soluble organic solvent such as a water-soluble alcohol, or may not contain a water-soluble organic solvent.

[0561] Furthermore, melt extrusion can be carried out by appropriately setting extrusion conditions as long as the extrusion conditions are generally such that pelletization is possible.

[0562] In the manufacturing method of the present disclosure, the obtained FEP may have terminal groups such as -CF3, -CF2H on at least one of the polymer main chain and polymer side chains, but it is preferable that the content of thermally unstable groups such as -COOH, -CH2OH, -COF, -CF=CF-, -CONH2, and -COOCH3 (hereinafter referred to as "unstable terminal groups") is low or absent.

[0563] The unstable terminal groups are chemically unstable and therefore not only reduce the heat resistance of the resin but also cause an increase in the attenuation of the resulting electric wire.

[0564] In the production method of the present disclosure, the polymer at the end of polymerization is prepared by subjecting the polymer to a polymerization reaction in which the total number of unstable terminal groups and -CFH terminal groups is 1×10 carbon atoms. 6 It is preferable to produce the carbon atoms so that the number of carbon atoms is 50 or less per unit. 6 The number of terminal groups per unit is preferably less than 20, and more preferably not more than 5. The unstable terminal groups and -CF2H terminal groups may be absent, and all may be -CF3 terminal groups.

[0565] Unstable terminal groups and -CF2H terminal groups can be converted to -CF3 terminal groups and stabilized by the fluorine radical treatment described above. The FEP used for this fluorine radical treatment can be in the form of a dry powder after polymerization or melt-extruded pellets.

[0566] The FEP obtained by the manufacturing method of the present disclosure has good moldability and is less likely to produce molding defects, and also has good heat resistance, chemical resistance, solvent resistance, insulating properties, electrical properties, etc.

[0567] The method for producing the above-mentioned FEP powder is a method for obtaining powder by drying and pulverizing the FEP obtained by the above-mentioned production method of the present disclosure.

[0568] The powder may be fluorinated. The method for producing the fluorinated powder is a method for obtaining the fluorinated powder by supplying fluorine gas to the powder obtained by the method for producing the powder described above to fluorinate the powder.

[0569] The method for producing FEP pellets is a method for obtaining pellets by pelletizing the FEP obtained by the production method of the present disclosure described above.

[0570] The pellets may be fluorinated. The method for producing fluorinated pellets is a method for obtaining fluorinated pellets by supplying fluorine gas to the pellets obtained by the above-described method for producing pellets, thereby fluorinating the pellets.

[0571] Therefore, this FEP can be used to produce various molded products such as covering materials for electric wires, foamed electric wires, cables, wires, etc., as well as tubes, films, sheets, filaments, etc.

[0572] (2) In the production method of the present disclosure, the polymerization of TFE / perfluoro(alkyl vinyl ether) copolymers such as PFA and MFA and TFE / perfluoroallyl ether copolymers is preferably carried out at a polymerization temperature of 10 to 100°C and a polymerization pressure of 0.3 to 6.0 MPaG.

[0573] The preferred monomer composition (mol %) of the TFE / perfluoro(alkyl vinyl ether) copolymer is TFE:perfluoro(alkyl vinyl ether)=(90-99.7):(0.3-10), more preferably (97-99):(1-3). The perfluoro(alkyl vinyl ether) is represented by the formula: CF2=CFORf 4 (In the formula, Rf 4 It is preferable to use one represented by a perfluoroalkyl group having 1 to 6 carbon atoms.

[0574] In addition to TFE and perfluoro(alkyl vinyl ether), other monomers copolymerizable with these monomers may be polymerized to obtain a copolymer of TFE, perfluoro(alkyl vinyl ether), and other monomers as a TFE / perfluoro(alkyl vinyl ether) copolymer. Examples of the other monomers include the above-mentioned fluorine-containing monomers (excluding TFE and perfluoro(alkyl vinyl ether)) and fluorine-free monomers. One or more types of other monomers may be used. The content of the other monomer units in the TFE / perfluoro(alkyl vinyl ether) copolymer may be 0.1 to 2% by mass based on the total monomer units.

[0575] The preferred monomer composition (mol%) of the TFE / perfluoroallyl ether copolymer is TFE:perfluoroallyl ether=(90-99.7):(0.3-10), more preferably (97-99):(1-3). The perfluoroallyl ether is represented by the formula: CF2=CFCF2ORf 4 (In the formula, Rf 4 It is preferable to use one represented by a perfluoroalkyl group having 1 to 6 carbon atoms.

[0576] In addition to TFE and perfluoroallyl ether, other monomers copolymerizable with these monomers may be polymerized to obtain a copolymer of TFE, perfluoroallyl ether, and other monomers as a TFE / perfluoroallyl ether copolymer. Examples of the other monomers include the above-mentioned fluorine-containing monomers (excluding TFE and perfluoroallyl ether) and non-fluorine-containing monomers. One or more types of other monomers may be used. The content of the other monomer units in the TFE / perfluoroallyl ether copolymer may be 0.1 to 2 mass% based on the total monomer units.

[0577] In the polymerization of the above TFE / perfluoro(alkyl vinyl ether) copolymer and TFE / perfluoroallyl ether copolymer, polymer (I) can be used within the range of use in the production method of the present disclosure, but it is usually preferable to add it in an amount of 0.0001 to 10 mass % relative to 100 mass % of the aqueous medium.

[0578] In the polymerization of the above TFE / perfluoro(alkyl vinyl ether) copolymer and TFE / perfluoroallyl ether copolymer, it is preferable to use cyclohexane, methanol, ethanol, propanol, propane, butane, pentane, hexane, carbon tetrachloride, chloroform, methylene chloride, methyl chloride, methane, ethane, or the like as a chain transfer agent, and it is preferable to use ammonium carbonate, disodium hydrogen phosphate, or the like as a pH buffer.

[0579] The aqueous dispersions of TFE / perfluoro(alkyl vinyl ether) copolymers such as PFA and MFA and TFE / perfluoroallyl ether copolymers obtained by the production method of the present disclosure may be subjected to post-treatment such as concentration as necessary, dried, powdered, and then melt-extruded to form pellets. The aqueous medium in the aqueous dispersion may contain additives such as nonionic surfactants as necessary, and may contain or not contain a water-soluble organic solvent such as a water-soluble alcohol.

[0580] Furthermore, melt extrusion can be carried out by appropriately setting extrusion conditions as long as the extrusion conditions are generally such that pelletization is possible.

[0581] The copolymer is preferably subjected to the above-mentioned fluorine radical treatment to improve its heat resistance and further enhance the chemical solution permeation suppression effect of the molded article. The above-mentioned fluorine radical treatment is also preferably performed to improve mechanical properties such as excellent tensile strength, improve flex resistance, and reduce heat weight loss. This can further improve the surface condition and non-stickiness of the molded article of the copolymer obtained. Furthermore, not only can the amount of eluted fluorine ions be significantly reduced, but the amount of eluted total organic carbon (TOC) can also be reduced. The water contact angle can be increased, improving liquid wettability and reducing metal ion elution.

[0582] As a result of the above-mentioned fluorine radical treatment, the unstable terminals of the copolymer are converted to -CF3 terminals, which make the copolymer thermally stable.

[0583] As a molding method for the copolymer and its composition, molding methods such as compression molding, transfer molding, extrusion molding, injection molding, and blow molding can be applied, as with conventional PFA.

[0584] Desired molded products can be obtained by such molding methods, and examples of molded products include sheets, films, packing, round bars, square bars, pipes, tubes, round tanks, square tanks, tanks, wafer carriers, wafer boxes, beakers, filter housings, flow meters, pumps, valves, cocks, connectors, nuts, electric wires, and heat-resistant electric wires.

[0585] Among these, it can be suitably used for tubes, pipes, tanks, connectors, etc. used in various chemical reaction equipment, semiconductor manufacturing equipment, and acid or alkaline chemical supply equipment, which require impermeability to chemicals.

[0586] Furthermore, a primer composition can be obtained by adding a nonionic surfactant to an aqueous dispersion of a TFE / perfluoro(alkyl vinyl ether) copolymer such as PFA or MFA and a TFE / perfluoroallyl ether copolymer, and, if necessary, dissolving or dispersing polyethersulfone, polyamideimide and / or polyimide, and metal powder in an organic solvent. This primer composition can also be used in a method for coating a metal surface with a fluororesin, which involves applying the primer composition to a metal surface, applying a melt-processable fluororesin composition onto the primer layer thus formed, and baking the melt-processable fluororesin composition layer together with the primer layer.

[0587] (3) The manufacturing method of the present disclosure can also be used to manufacture an electrolyte polymer precursor. In the manufacturing method of the present disclosure, the polymerization of the electrolyte polymer precursor is preferably carried out at a polymerization temperature of 10 to 100°C and a polymerization pressure of 0.1 to 2.0 MPaG. The electrolyte polymer precursor is a polymer containing -SO2X 151 , -COZ 151 or -POZ 152 Z 153 (X 151 , Z 151 , Z 152 and Z 153 The ion-exchange polymer is composed of a monomer containing a functional group represented by the formula (which will be described later), and can be converted into an ion-exchange polymer through hydrolysis treatment.

[0588] Monomers used in the electrolyte polymer precursor include: General formula (150): CF2=CF-O-(CF2CFY 151 -O) n -(CFY 152 ) m -A 151 (In the formula, Y 151 represents a fluorine atom, a chlorine atom, a -SO2F group, or a perfluoroalkyl group. The perfluoroalkyl group may contain an etheric oxygen and a -SO2F group. n represents an integer of 0 to 3. n Y 151 may be the same or different. 152represents a fluorine atom, a chlorine atom, or a -SO2F group. m represents an integer of 1 to 5. m Y 152 may be the same or different. 151 -SO2X 151 , -COZ 151 or -POZ 152 Z 153 represents X 151 are F, Cl, Br, I, -OR 151 or -NR 152 R 153 Represents Z. 151 , Z 152 and Z 153 are the same or different and are -NR 154 R 155 -OR 156 Represents R 151 , R 152 , R 153 , R 154 , R 155 and R 156 are the same or different and represent H, ammonium, alkali metal, an alkyl group which may contain a fluorine atom, an aryl group, or a sulfonyl-containing group. Examples of the fluoromonomers represented by the formula: are listed below. Examples of the monomers used for the electrolyte polymer precursor include compounds containing two fluorosulfonyl groups described in WO 2007 / 013532 and perfluoromonomers having a -SO2F group and a dioxolane ring described in WO 2014 / 175123. The preferred monomer composition (mol %) of the electrolyte polymer precursor is TFE:vinyl ether = (50-99):(50-1), and more preferably TFE:vinyl ether = (50-93):(50-7).

[0589] The electrolyte polymer precursor may be modified with a third monomer in an amount of 0 to 20% by mass of the total monomers. Examples of the third monomer include CTFE, vinylidene fluoride, perfluoroalkyl vinyl ether, perfluorobutenyl vinyl ether, cyclic monomers such as perfluoro-2,2-dimethyl-1,3-dioxolane and perfluoro-2-methylene-4-methyl-1,3-dioxole, and polyfunctional monomers such as divinylbenzene.

[0590] The electrolyte polymer precursor thus obtained can be formed into a membrane, for example, and then subjected to hydrolysis with an alkaline solution and treatment with a mineral acid, resulting in a polymer electrolyte membrane that can be used in fuel cells, electrolysis devices, redox flow batteries, and the like. Alternatively, an electrolyte polymer dispersion can be obtained by subjecting the electrolyte polymer precursor to hydrolysis with an alkaline solution while maintaining the dispersed state of the electrolyte polymer precursor. Subsequently, by heating to 120° C. or higher in a pressure vessel, the compound can be dissolved in, for example, a water / alcohol mixed solvent to form a solution. The solution thus obtained can be used, for example, as a binder for electrodes, or can be combined with various additives to form a cast film, which can be used, for example, as an antifouling coating film or an organic actuator.

[0591] The melt-processible fluororesin powder can be produced by drying and powdering the melt-processible fluororesin obtained by the production method of the present disclosure. The production method for producing the melt-processible fluororesin powder also constitutes part of the present disclosure.

[0592] In the production method of the present disclosure, when the fluoropolymer is coagulated, washed, dried, or the like, wastewater and off-gas are generated. The polymer (I), decomposition products and by-products of the polymer (I), and residual monomers produced as by-products from the polymer (I) can be recovered and purified from the wastewater generated by the coagulation or washing and / or the off-gas generated by drying, allowing the polymer (I), decomposition products and by-products of the polymer (I), and residual monomers can be reused. The recovery and purification methods are not particularly limited, and can be carried out by known methods. For example, the methods described in JP-A-2011-520020 and the methods described in U.S. Patent Application Publication Nos. 2007 / 15937, 2007 / 25902, and 2007 / 27251 are examples. Specific examples include the following methods.

[0593] Examples of a method for recovering the polymer (I), decomposition products and by-products of the polymer (I), residual monomers, etc., from the wastewater include a method of contacting the wastewater with adsorption particles such as ion exchange resin, activated carbon, silica gel, clay, zeolite, etc., to adsorb the polymer (I), etc., and then separating the wastewater from the adsorption particles. Incineration of the adsorption particles that have adsorbed the polymer (I), etc., can prevent the release of the polymer (I), etc., into the environment.

[0594] Alternatively, the polymer (I) or the like can be recovered by desorbing and eluting it from ion exchange resin particles that have adsorbed the polymer (I) or the like using a known method. For example, when the ion exchange resin particles are anion exchange resin particles, the polymer (I) or the like can be eluted by contacting a mineral acid with the anion exchange resin. Subsequently, when a water-soluble organic solvent is added to the resulting eluate, the mixture usually separates into two phases. The lower phase containing the polymer (I) or the like can be recovered by neutralizing it. Examples of the water-soluble organic solvent include polar solvents such as alcohols, ketones, and ethers.

[0595] Other methods for recovering the polymer (I) and the like from the ion exchange resin particles include a method using an ammonium salt and a water-soluble organic solvent, and a method using an alcohol and, if desired, an acid. In the latter method, an ester derivative of the polymer (I) and the like is produced, which can be easily separated from the alcohol by distillation.

[0596] If the wastewater contains fluoropolymer particles or other solids, it is preferable to remove them before contacting the wastewater with the adsorbent particles. Methods for removing the fluoropolymer particles and other solids include a method in which they are precipitated by adding an aluminum salt or the like, and then the precipitate is separated from the wastewater, or electrocoagulation. Mechanical methods, such as crossflow filtration, depth filtration, and precoat filtration, may also be used for removal. The concentration of the unagglomerated fluoropolymer in the wastewater is preferably low from the viewpoint of productivity, more preferably less than 0.4 mass %, particularly preferably less than 0.3 mass %.

[0597] A method for recovering the polymer (I) and the like from the off-gas includes using a scrubber to contact the off-gas with deionized water, an aqueous alkali solution, an organic solvent such as a glycol ether solvent, etc., to obtain a scrubber solution containing the polymer (I) and the like. When a highly concentrated aqueous alkali solution is used as the aqueous alkali solution, the scrubber solution can be recovered in a state in which the polymer (I) and the like are phase-separated, facilitating the recovery and reuse of the polymer (I) and the like. Examples of the alkaline compound include alkali metal hydroxides and quaternary ammonium salts.

[0598] The scrubber solution containing the polymer (I) and the like may be concentrated using a reverse osmosis membrane or the like. The concentrated scrubber solution usually contains fluoride ions, but by adding alumina after concentration to remove the fluoride ions, it is possible to facilitate the reuse of the polymer (I) and the like. Alternatively, the scrubber solution may be brought into contact with adsorbent particles to adsorb the polymer (I) and the like, and the polymer (I) and the like may be recovered by the method described above.

[0599] The polymer (I) and the like recovered by any of the above methods can be reused in the production of a fluoropolymer.

[0600] Although the embodiments have been described above, it will be understood that various changes in form and details can be made without departing from the spirit and scope of the claims. [Example]

[0601] Next, embodiments of the present disclosure will be described with reference to examples, but the present disclosure is not limited to these examples.

[0602] The values ​​in the examples were measured by the following methods.

[0603] <Solid content concentration> 1 g of the aqueous dispersion was dried in a blower dryer at 150°C for 60 minutes, and the ratio of the mass of the heating residue to the mass (1 g) of the aqueous dispersion was expressed as a percentage and used as the value.

[0604] <Average primary particle diameter> The average primary particle size was measured by dynamic light scattering. For dynamic light scattering, an aqueous dispersion with a solids concentration of approximately 1.0% by mass was prepared, and measurements were taken at 25°C with an ELSZ-1000S (Otsuka Electronics Co., Ltd.) for a total of 70 measurements. The refractive index of the solvent (water) was 1.3328, and the viscosity of the solvent (water) was 0.8878 mPa s.

[0605] <Aspect ratio> An aqueous dispersion diluted to a solids concentration of approximately 1% by mass was observed using a scanning electron microscope (SEM). Images of more than 400 randomly selected particles were processed, and the average ratio of their major and minor diameters was calculated.

[0606] <Standard specific gravity (SSG)> Using samples molded in accordance with ASTM D4895-89, measurements were made by the water displacement method in accordance with ASTM D-792.

[0607] <Peak temperature> The temperature corresponding to the maximum value appearing on the differential thermal (DTA) curve obtained by heating the PTFE powder at a temperature rate of 10°C / min using a TG / DTA (thermogravimetric / differential thermal analyzer) was taken as the peak temperature.

[0608] <Modified Monomer Content> The HFP content was determined by press-molding PTFE powder to create a thin film disk, and measuring the infrared absorbance of the thin film disk by FT-IR. -1 Absorbance at / 935cm -1 The absorbance ratio was calculated by multiplying the absorbance ratio by 0.3. The content of CH2=CF(CF2OCFCF3COONH4) (hereinafter also referred to as "modified monomer a") was calculated from the total amount of modified monomer a charged.

[0609] <Content of Polymer A> The content of polymer A in the PTFE powder is 19 It was calculated using the following formula from the spectrum obtained by F-MAS NMR measurement. Y = (4B / (5A+3B)) x 100 Y: Polymer A content (mol%) A: Integrated value of the signal at -120 ppm B: Sum of integrals of CF2 and CF3 signals at -83 ppm The chemical shift value was determined by setting the peak top of the signal derived from the main chain of PTFE at −120 ppm. The quantitation limit of polymer A by this measurement method is 10 ppm by mass.

[0610] In the examples, a homopolymer of CH2=CF(CF2OCFCF3COONH4) (modified monomer a) (number average molecular weight 9×10 4 , weight average molecular weight 19×10 4 ) (hereinafter referred to as "Polymer A") was used. The number-average molecular weight and weight-average molecular weight were measured by gel permeation chromatography (GPC) using a Tosoh GPC HLC-8020 column and Shodex columns (one GPC KF-801, one GPC KF-802, and two GPC KF-806M columns connected in series) using tetrahydrofuran (THF) as the solvent at a flow rate of 1 ml / min, and the molecular weight was calculated using monodisperse polystyrene as the standard.

[0611] Example 1 A 6 L stainless steel reactor equipped with a stirrer was charged with 3560 g of deionized water, 104 g of paraffin wax, 5.37 g of polymer A, and 77.3 mg of modified monomer A. The pH was adjusted to 9.1 by adding aqueous ammonia. The reactor contents were then heated to 70 °C while evacuating and simultaneously purging with TFE to remove oxygen from the reactor, and the contents were stirred. 0.8 g of HFP was added to the reactor, followed by TFE addition until the pressure reached 0.73 MPaG. 17.9 mg of ammonium persulfate (APS) initiator dissolved in 20 g of deionized water was injected into the reactor, bringing the reactor pressure to 0.83 MPaG. After the initiator injection, a pressure drop occurred and polymerization initiation was observed. TFE was added to the reactor to maintain a constant pressure of 0.78 MPaG. When approximately 180 g of TFE had been consumed in the reaction, the TFE supply and stirring were stopped. The gas in the reactor was then slowly released until the reactor pressure reached 0.02 MPaG. TFE was then supplied until the reactor pressure reached 0.78 MPaG, and stirring was resumed to continue the reaction. When approximately 540 g of TFE had been consumed in the reaction, 14.3 mg of hydroquinone dissolved in 20 g of deionized water was added to the reactor, and the reaction was continued. When approximately 1250 g of TFE had been consumed in the reaction, the supply of TFE was stopped, stirring was stopped, and the reaction was terminated. The reactor was then vented to atmospheric pressure, and the contents (aqueous PTFE dispersion) were removed from the reactor and cooled. The supernatant paraffin wax was removed from the aqueous PTFE dispersion. The physical properties of the resulting aqueous PTFE dispersion are shown below. Solid concentration of PTFE aqueous dispersion: 25.7% by mass PTFE average primary particle size: 249 nm PTFE aspect ratio: 1.38

[0612] The resulting PTFE aqueous dispersion was diluted with deionized water to a solids concentration of approximately 10% by mass, coagulated under high-speed stirring conditions, and the coagulated wet powder was dried for 18 hours at 210° C. The physical properties of the resulting PTFE powder are shown below. Standard specific gravity of PTFE powder: 2.172 PTFE powder peak temperature: 343℃ HFP content of PTFE: 0.031% by mass PTFE modified monomer a content: 0.006% by mass Content of polymer A relative to PTFE in PTFE powder: 0.43 mass% As described above, it was found that the obtained PTFE powder was a composition containing PTFE and polymer A.

[0613] 30 g of the PTFE powder obtained above was placed in a reactor. The reactor was heated to 200 °C and then purged with nitrogen for 1 hour to remove the air from the reactor. While maintaining the temperature at 200 °C, a mixed gas (fluorine gas (F2) diluted with nitrogen gas (volume ratio: 20 / 80)) was flowed continuously at a flow rate of approximately 50 mL / min for 480 minutes (8 hours) at atmospheric pressure (1 atm) (fluorine radical source added amount (i.e., fluorine gas amount): 7.5 g). After the reaction was completed, the system was immediately purged with nitrogen gas for 1 hour to remove the fluorine gas. A starch / iodide test was performed to confirm the absence of fluorine gas in the inert gas by the presence or absence of color development of the indicator. The reactor was cooled to room temperature, and the PTFE powder was recovered. The content of polymer A in the PTFE powder was below the quantitation limit for PTFE.

[0614] Furthermore, the content of high-temperature volatile matter and coloration of the PTFE powder before and after the fluorine radical treatment were evaluated by the following methods.

[0615] <High-temperature volatile content evaluation> Approximately 10 g of PTFE powder was placed in an aluminum cup (volume 50 ml, upper diameter 61 mm, lower diameter 42 mm, depth 33 mm) and held for 2 hours in an atmosphere of 370±2°C in a hot air circulation electric furnace that had been adjusted to the heating temperature in advance.The weight was then measured and the content of high-temperature volatile matter was calculated using the following formula. High-temperature volatile content (mass%) = (weight (g) of PTFE powder before heat treatment - weight (g) of PTFE powder after heat treatment) / weight (g) of PTFE powder before heat treatment × 100

[0616] The content of high-temperature volatile matter in the PTFE powder before the fluorine radical treatment was 0.34% by mass, and the content of high-temperature volatile matter in the PTFE powder after the fluorine radical treatment was 0.10% by mass.

[0617] <Coloring evaluation> The color tone (L* value, Z value) of the PTFE powder was measured in accordance with JIS Z 8781-4 using a colorimeter ZE-6000 (manufactured by Nippon Denshoku Industries Co., Ltd.) (CIELAB color scale).

[0618] The method for preparing a PTFE sample for measuring color tone (L* value, Z value) is as follows. 4.0 g of PTFE powder was weighed and placed in a cylindrical mold with an inner diameter of 28.6 mm, and held at a pressure of 8.27 MPa for 1 minute to produce a disk-shaped PTFE molded body (unsintered) with a thickness of approximately 4 mm. After removing the disk-shaped PTFE molded body from the mold, it was left at 25°C for 24 hours. The color tone (L* value, Z value) of the disc-shaped PTFE molded article (unsintered) was measured using a color difference meter.

[0619] The color tone of the PTFE molded product before the fluorine radical treatment was an L* value of 91.2 and a Z value of 90.7. The color tone of the PTFE molded product after the fluorine radical treatment was an L* value of 98.1 and a Z value of 112.8.

Claims

1. A method for producing a high-purity fluoropolymer-containing composition, comprising: subjecting a composition containing a fluoropolymer and a polymer (I) comprising polymerization units (I) based on a monomer (I) represented by general formula (I) to fluorine radical treatment to obtain a high-purity fluoropolymer-containing composition. CX １ X ３ =CX ２ R(-CZ １ Z ２ -A ０ ) ｍ (I) (In the formula, X １ and X ３ are each independently F, Cl, H or CF ３ and X ２ is H, F, an alkyl group or a fluorine-containing alkyl group; A ０ is an anionic group; R is a linking group; Z １ and Z ２ are each independently H, F, an alkyl group or a fluorine-containing alkyl group; and m is an integer of 1 or more.

2. A in general formula (I) ０ But, -SO ３ M, -COOM or -P(O)(OM) ２ (In each formula, M is H, metal atom, NR ７ ４ , optionally substituted imidazolium, optionally substituted pyridinium, or optionally substituted phosphonium, and R ７ is H or an organic group.

3. A in general formula (I) ０ -COOM (wherein M is H, a metal atom, NR ７ ４ , optionally substituted imidazolium, optionally substituted pyridinium, or optionally substituted phosphonium, and R ７ The method according to claim 1 or 2, wherein:

4. 4. The method according to claim 1, wherein the ion exchange capacity of the polymer (I) is 1.75 meq / g or more.

5. 5. The process according to claim 1, wherein the ion exchange capacity of the polymer (I) is 2.60 meq / g or more.

6. The method according to any one of claims 1 to 5, wherein m in general formula (I) is 1.

7. The method according to any one of claims 1 to 6, wherein the fluoropolymer is polytetrafluoroethylene.

8. The process according to any one of claims 1 to 7, wherein a composition containing the fluoropolymer and polymer (I) is obtained by polymerizing a fluoromonomer in the presence of the polymer (I).

9. A fluoromonomer is polymerized in an aqueous medium in the presence of the polymer (I) to obtain an aqueous dispersion containing the fluoropolymer, the polymer (I), and an aqueous medium, and then The method according to any one of claims 1 to 8, wherein the composition containing the fluoropolymer and polymer (I) is obtained by coagulating the aqueous dispersion.

10. 10. The process according to claim 8 or 9, wherein the fluoromonomer is polymerized substantially in the absence of a fluorine-containing surfactant.

11. The method according to any one of claims 8 to 10, wherein the fluoromonomer is tetrafluoroethylene or a modified monomer copolymerizable with tetrafluoroethylene.

12. The method according to any one of claims 8 to 10, wherein the fluoromonomer is at least one selected from the group consisting of hexafluoropropylene, perfluoro(alkyl vinyl ether), and perfluoroallyl ether, and tetrafluoroethylene.

13. A high-purity fluoropolymer-containing composition obtained by the production method according to any one of claims 1 to 12.

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