Method for producing fluorine-containing polymer, aqueous dispersion, particles, and composition

Abstract

To provide a composition containing a fluorine-containing polymer having excellent heat resistance without necessarily requiring a fluorine-containing emulsifier. [Solution] A composition containing a first perfluoropolymer having a glass transition temperature of 10°C or lower and a second fluoropolymer which contains structural units based on tetrafluoroethylene and structural units based on hexafluoropropylene and is different from the first perfluoropolymer, wherein the content of structural units based on perfluoro(alkyl vinyl ether) is 0.1 to 5.0 mol% relative to the total content of all structural units of the first perfluoropolymer and the second fluoropolymer.

Description

[Technical Field]

[0001] The present invention relates to a method for producing a fluorine-containing polymer, an aqueous dispersion, particles and a composition. [Background technology]

[0002] Fluorine-containing polymers such as tetrafluoroethylene copolymers are used in various industrial fields because of their excellent heat resistance, chemical resistance, flame retardancy, weather resistance, and the like. As a method for producing a fluorine-containing polymer, there is mentioned a method in which a fluorine-containing emulsifier is used to emulsion-polymerize a fluorine-containing monomer in an aqueous medium (see Patent Document 1). [Prior art documents] [Patent documents]

[0003] [Patent Document 1] International Publication No. 2007 / 046377 Summary of the Invention [Problem to be solved by the invention]

[0004] The method for producing a fluorinated polymer disclosed in Patent Document 1 uses an aqueous medium and therefore has a small environmental impact, but when a large amount of a fluorinated emulsifier, which is an essential component, remains in the aqueous dispersion obtained by polymerization, it becomes necessary to remove the fluorinated emulsifier depending on the application. Moreover, in recent years, there has been a trend toward restricting the use of fluorinated emulsifiers.

[0005] The present disclosure has been made in view of the above circumstances, and an object of one embodiment of the present invention is to provide a composition containing a fluorinated polymer having excellent heat resistance without requiring a fluorinated emulsifier as an essential component. Furthermore, a problem to be solved by one embodiment of the present invention is to provide a method for producing a fluoropolymer which is capable of producing a fluoropolymer having excellent heat resistance without requiring a fluorinated emulsifier as an essential component. Furthermore, a problem to be solved by one embodiment of the present invention is to provide an aqueous dispersion containing a fluorine-containing polymer that is excellent in heat resistance. Furthermore, a problem to be solved by one embodiment of the present invention is to provide particles containing a fluoropolymer that are excellent in heat resistance. [Means for solving the problem]

[0006] The present disclosure includes the following aspects. [1] a first perfluoropolymer having a glass transition temperature of 10°C or less; a second fluoropolymer that contains tetrafluoroethylene-based structural units and hexafluoropropylene-based structural units and is different from the first perfluoropolymer; A composition in which the content of structural units based on perfluoro(alkyl vinyl ether) is 0.1 to 5.0 mol % relative to the total content of all structural units of the first perfluoropolymer and the second fluoropolymer. [2] Neither the first perfluoropolymer nor the second fluoropolymer contains a functional group, or the first perfluoropolymer and the second fluoropolymer have a main chain carbon number of 10 or less. 6 The composition according to [1], wherein the total number of functional groups per unit is less than 100. [3] The composition according to [1] or [2], wherein the first perfluoropolymer contains a structural unit based on tetrafluoroethylene and a structural unit based on perfluoro(alkyl vinyl ether). [4] The composition according to [3], wherein in the first perfluoropolymer, the constituent units based on perfluoro(alkyl vinyl ether) account for 20 to 70 mol % of the constituent units based on tetrafluoroethylene and the constituent units based on perfluoro(alkyl vinyl ether). [5] A step of preparing an aqueous dispersion A containing a first perfluoropolymer having a glass transition temperature of 10°C or less and an aqueous medium; and polymerizing, in the aqueous dispersion A, monomers including tetrafluoroethylene and hexafluoropropylene to produce a second fluoropolymer different from the first perfluoropolymer; before the start of polymerization of the monomers, the content of the first perfluoropolymer is 0.01 to 4.0% by mass relative to the total mass of the aqueous dispersion A; A method for producing a fluorine-containing polymer, wherein, before the start of polymerization of monomers, aqueous dispersion A does not contain a fluorine-containing emulsifier, or the content of the fluorine-containing emulsifier in aqueous dispersion A is 100 ppm by mass or less, based on the total mass of aqueous dispersion A. [6] The method for producing a fluorine-containing polymer according to [5], wherein the amount of the monomer used is 1 to 50 parts by mass per 100 parts by mass of the aqueous medium used. [7] the step of preparing an aqueous dispersion A is a step of preparing an aqueous dispersion A containing particles of a first perfluoropolymer and an aqueous medium, the step of producing the second fluoropolymer is a step of polymerizing a monomer to produce a second fluoropolymer different from the first perfluoropolymer, and producing particles containing the first perfluoropolymer and the second fluoropolymer; The method for producing a fluoropolymer according to [5] or [6], wherein the ratio of the average particle size of the particles comprising the first perfluoropolymer and the second fluoropolymer to the average particle size of the particles of the first perfluoropolymer is 2 or more. [8] The method for producing a fluorine-containing polymer according to any one of [5] to [7], wherein the viscosity of the aqueous dispersion A is 2.0 mPa·s or less. [9] The method for producing a fluorine-containing polymer according to any one of [5] to [8], wherein the aqueous dispersion A has a thixotropy ratio of 0.9 to 1.2.

[10] The method for producing a fluorine-containing polymer according to any one of [5] to [9], wherein the monomers are polymerized in the presence of a polymerization initiator.

[11] The method for producing a fluorinated polymer according to any one of [5] to

[10] , further comprising a step of subjecting the first perfluoropolymer and the second fluoropolymer to a fluorination treatment.

[12] An aqueous dispersion comprising an aqueous medium and melt-formable particles, The average particle size of the particles is 1 μm or less, the particles contain one or more fluorine-containing polymers, the fluorine-containing polymer contains a structural unit based on tetrafluoroethylene, a structural unit based on perfluoro(alkyl vinyl ether), and a structural unit based on hexafluoropropylene, the content of structural units based on perfluoro(alkyl vinyl ether) is 0.1 to 5.0 mol % based on all structural units of the fluorine-containing polymer, the particle content is 1 to 50% by mass based on the total mass of the aqueous dispersion, An aqueous dispersion which does not contain a fluorine-containing emulsifier or the content of the fluorine-containing emulsifier is 100 ppm by mass or less relative to the content of the fluorine-containing polymer.

[13] The aqueous dispersion according to

[12] , having a viscosity of 0.8 to 2.0 mPa·s.

[14] 1. A melt-formable particle comprising: The average particle size of the particles is 1 μm or less, the particles contain one or more fluorine-containing polymers, the fluorine-containing polymer contains a structural unit based on tetrafluoroethylene, a structural unit based on perfluoro(alkyl vinyl ether), and a structural unit based on hexafluoropropylene, the content of structural units based on perfluoro(alkyl vinyl ether) is 0.1 to 5.0 mol % based on all structural units of the fluorine-containing polymer, does not contain a fluorine-containing emulsifier, or the content of the fluorine-containing emulsifier is 100 ppm by mass or less relative to the content of the fluorine-containing polymer, Particles having a content of the compound represented by formula (S1) of 1 to 10,000 ppb by mass and a content of the compound represented by formula (S2) of 100 ppb by mass or less, relative to the fluorine-containing polymer. Formula (S1):H-(CF2) n -COOM Formula (S2):H-(CF2) m -SO3M In formula (S1) and formula (S2), M each independently represents a hydrogen atom, Na, K, or NH4; n represents 7 to 11; and m represents 8 to 12. [Effects of the Invention]

[0007] According to one embodiment of the present invention, there is provided a composition containing a fluorine-containing polymer having excellent heat resistance, without requiring a fluorine-containing emulsifier as an essential component. Furthermore, according to one embodiment of the present invention, there is provided a method for producing a fluoropolymer which is capable of producing a fluoropolymer having excellent heat resistance without requiring a fluorinated emulsifier as an essential component. Furthermore, according to one embodiment of the present invention, there is provided an aqueous dispersion containing a fluorine-containing polymer having excellent heat resistance. Furthermore, according to one embodiment of the present invention, there are provided particles containing a fluorine-containing polymer having excellent heat resistance. DETAILED DESCRIPTION OF THE INVENTION

[0008] In the present disclosure, numerical ranges indicated using "to" include the numerical values ​​before and after "to" as the minimum and maximum values, respectively. In the present disclosure, in which numerical ranges are described in stages, the upper or lower limit value described in one numerical range may be replaced with the upper or lower limit value of another numerical range described in stages. In addition, in the numerical ranges described in this specification, the upper or lower limit value of the numerical range may be replaced with a value shown in the examples. In the present disclosure, when a plurality of substances corresponding to each component are present in the composition, the amount of each component in the composition means the total amount of the plurality of substances present in the composition, unless otherwise specified. In the present disclosure, a combination of two or more preferred embodiments is a more preferred embodiment. In the present disclosure, the term "process" includes not only an independent process but also a process that cannot be clearly distinguished from other processes, as long as the intended purpose of the process is achieved.

[0009] [Composition] The composition of the present disclosure contains a first perfluoropolymer having a glass transition temperature of 10°C or lower, and a second fluoropolymer that contains structural units based on tetrafluoroethylene (hereinafter also referred to as "TFE") (hereinafter also referred to as "TFE units") and structural units based on hexafluoropropylene (hereinafter also referred to as "HFP") (hereinafter also referred to as "HFP units") and is different from the first perfluoropolymer, and the content of structural units based on perfluoro(alkyl vinyl ether) (hereinafter also referred to as "PAVE") (hereinafter also referred to as "PAVE units") relative to the total content of all structural units of the first perfluoropolymer and the second fluoropolymer is 0.1 to 5.0 mol%.

[0010] The composition of the present disclosure contains a first perfluoropolymer and a second fluoropolymer, and has excellent heat resistance because the content of PAVE units relative to the total content of all structural units of the first perfluoropolymer and the second fluoropolymer is 0.1 to 5.0 mol %.

[0011] In contrast, Patent Document 1 does not mention a composition containing two or more types of fluorine-containing copolymers.

[0012] (First perfluoropolymer) The first perfluoropolymer is a perfluoropolymer having a glass transition temperature of 10°C or less. In this disclosure, "perfluoropolymer" means a polymer in which all hydrogen atoms bonded to carbon atoms in the structural units of the polymer are substituted with fluorine atoms. "fluoropolymer" means a polymer in which some or all of the hydrogen atoms bonded to carbon atoms in the structural units of the polymer are substituted with fluorine atoms.

[0013] The glass transition temperature (hereinafter also referred to as "Tg") of the first perfluoropolymer is 10°C or lower. The Tg of the first perfluoropolymer is preferably 5° C. or lower, more preferably 3° C. or lower, and even more preferably 0° C. or lower, from the viewpoint of efficiently adsorbing the specific monomer described below. From the viewpoint of thermal stability after molding, the Tg of the first perfluoropolymer is preferably −50° C. or higher, more preferably −45° C. or higher, and even more preferably −40° C. or higher.

[0014] The Tg of the first perfluoropolymer is measured by differential scanning calorimetry (DSC). For example, Tg is measured using a NEXTA DSC600 manufactured by Hitachi High-Technologies Corporation. Specifically, 5 mg of the sample to be measured is weighed into an aluminum sample pan, and the sample is heated to 100°C at a heating rate of 10°C / min under a nitrogen atmosphere. It is then cooled to -60°C at a rate of 10°C / min. Once the specified temperature is reached, the temperature is again raised to 100°C at 10°C / min. Tg is estimated from the inflection point observed during this second heating operation.

[0015] As a method for adjusting the Tg of the first perfluoropolymer within the above range, for example, a method of adjusting the type and amount of the monomer used in producing the first perfluoropolymer can be mentioned.

[0016] The first perfluoropolymer preferably contains TFE units and PAVE units, since this makes it easier to adjust the Tg to the above range and provides better heat resistance.

[0017] The PAVE is preferably a monomer represented by formula (1) because it has excellent polymerization reactivity when producing the first perfluoropolymer. CF2=CF-OR f1 …(1) In formula (1), R f1 represents a perfluoroalkyl group having 1 to 10 carbon atoms. The number of carbon atoms in Rf1 is preferably 1 to 8, more preferably 1 to 6, still more preferably 1 to 5, and particularly preferably 1 to 3, in terms of better polymerization reactivity. The perfluoroalkyl group may be linear or branched.

[0018] Specific examples of PAVE include perfluoro(methyl vinyl ether) (hereinafter also referred to as "PMVE"), perfluoro(ethyl vinyl ether) (hereinafter also referred to as "PEVE"), and perfluoro(propyl vinyl ether) (hereinafter also referred to as "PPVE").

[0019] Among these, the PAVE is preferably PMVE or PPVE, more preferably PMVE, in terms of enabling more efficient production of the second fluoropolymer.

[0020] When the first perfluoropolymer contains TFE units and PAVE units, the content of PAVE units relative to the total content of TFE units and PAVE units in the first perfluoropolymer is preferably 20.0 to 70.0 mol%, more preferably 25.0 to 65.0 mol%, and even more preferably 30.0 to 60.0 mol%, from the viewpoint of facilitating adjustment of Tg within the above range.

[0021] The first perfluoropolymer may contain structural units based on monomers other than TFE and PAVE. From the viewpoint of more efficient production of the second fluoropolymer, the structural units based on other monomers are preferably 20.0 mol% or less, more preferably 15.0 mol% or less, based on the total structural units of the first perfluoropolymer. It is further preferred that the first perfluoropolymer is substantially free of structural units based on other monomers. "Substantially free of units derived from other monomers" means that the content of units derived from other monomers is 0.01 mol % or less based on the total constitutional units of the first perfluoropolymer. However, 0.00 mol % is more preferable. When a structural unit based on another monomer is contained, the other monomer is preferably hexafluoropropylene.

[0022] (Second Fluoropolymer) The second fluoropolymer is a different fluoropolymer than the first perfluoropolymer. The second fluoropolymer comprises TFE units and HFP units.

[0023] In the second fluoropolymer, the content of HFP units relative to the total content of TFE units and HFP units is preferably from 1.0 to 15.0 mol %, more preferably from 1.0 to 13.0 mol %, and even more preferably from 1.0 to 11.0 mol %, from the viewpoint of heat resistance. In the second fluoropolymer, the content of HFP units relative to the total content of TFE units and HFP units is preferably 1.0 to 20.0 mol %, more preferably 3.0 to 18.0 mol %, and even more preferably 5.0 to 15.0 mol %, from the viewpoint of mechanical properties.

[0024] The second fluoropolymer may contain structural units based on other monomers other than TFE and HFP, but from the viewpoint of heat resistance, the structural units based on other monomers are preferably 10.0 mol% or less, more preferably 5.0 mol% or less, based on the total structural units of the second fluoropolymer. It is even more preferable that the second fluoropolymer does not substantially contain structural units based on other monomers. Substantially free of units based on other monomers means that the content of units based on other monomers is 0.01 mol % or less, more preferably 0.00 mol %, relative to the total structural units of the second fluoropolymer. When a structural unit based on another monomer is contained, examples of the other monomer include fluoroolefins such as PAVE (excluding TFE and HFP); and acid anhydrides such as itaconic anhydride, citraconic anhydride, and 5-norbornene-2,3-dicarboxylic anhydride.

[0025] In the composition of the present disclosure, the content of PAVE units relative to the total content of all structural units of the first perfluoropolymer and the second fluoropolymer is 0.1 to 5.0 mol%, preferably 0.1 to 4.0 mol%, more preferably 0.1 to 3.0 mol%, and since the content of PAVE units is 0.1 to 5.0 mol%, the composition has excellent heat resistance.

[0026] The content of the first perfluoropolymer in the solid content of the composition of the present disclosure is preferably 0.01% by mass or more, and more preferably 0.1% by mass or more. The content of the first perfluoropolymer in the composition of the present disclosure is preferably 10% by mass or less, and more preferably 5% by mass or less.

[0027] The content of the second fluoropolymer in the solid content of the composition of the present disclosure is preferably 90 mass % or more, and more preferably 95 mass % or more. The content of the second fluoropolymer in the composition of the present disclosure is preferably 99.99% by mass or less, more preferably 99.9% by mass or less.

[0028] In the composition of the present disclosure, the content of the first perfluoropolymer relative to the total content of the first perfluoropolymer and the second fluoropolymer is preferably 0.2 mass% or more, more preferably 0.5 mass% or more, from the viewpoint of polymerization stability. The content of the first perfluoropolymer relative to the total content of the first perfluoropolymer and the second fluoropolymer is preferably 10 mass% or less, more preferably 5 mass% or less, from the viewpoint of heat resistance.

[0029] In order to have better heat resistance, the first perfluoropolymer and the second fluoropolymer do not contain any functional group, or the first perfluoropolymer and the second fluoropolymer have a main chain carbon number of 10 or less. 6 The total number of functional groups per unit is preferably less than 100, more preferably 50 or less, and even more preferably 30 or less.

[0030] Infrared spectroscopy can be used to identify the type of functional group and measure the number of functional groups.

[0031] The number of functional groups is measured by the following method. The first perfluoropolymer and the second fluoropolymer are press-molded at 340° C. to prepare a film having a thickness of 200 μm. The film is scanned 16 times by a Fourier transform infrared spectrometer and analyzed to obtain an infrared absorption spectrum. The first perfluoropolymer and the second fluoropolymer are subjected to a fluorination treatment for a long period of time in the fluorination step described below to obtain a fully fluorinated first perfluoropolymer and a fully fluorinated second fluoropolymer. The fully fluorinated first perfluoropolymer and the fully fluorinated second fluoropolymer are press-molded at 340°C to produce a fully fluorinated film with a thickness of 200 μm. The fully fluorinated film is scanned 16 times using a Fourier transform infrared spectrometer and analyzed to obtain a base spectrum. From the absorption peaks of specific functional groups that appear in the difference spectrum between the obtained infrared absorption spectrum and the base spectrum, the compound having 10 main chain carbon atoms can be determined by the following formula (A). 6 Calculate the number of functional groups per molecule, N. N=I×K / t …(A) I: Absorbance K: Correction coefficient t: film thickness (mm)

[0032] Table 1 shows the absorption frequency, molar absorption coefficient, and correction factor for specific functional groups such as -CF2H. The molar absorption coefficient for a specific functional group is determined from FT-IR measurement data of a low molecular weight model compound.

[0033] [Table 1]

[0034] In the copolymers, the absorption frequencies of -CH2CF2H, -CH2COF, -CH2COOH, -CH2COOCH3, and -CH2CONH2 are calculated by multiplying the absorption frequencies of -CF2H, -COF, -COOH (free and bonded), -COOCH3, and -CONH2 shown in the table by several tens of Kaiser (cm -1 ) becomes lower. For example, the number of -COF is the absorption frequency of 1883 cm due to -CF2COF.-1 The number of functional groups determined from the absorption peak of -CH2COF and the absorption frequency of 1840 cm -1 The number of functional groups is the sum of the number of functional groups determined from the absorption peaks of the

[0035] The functional groups in the first perfluoropolymer and the second fluoropolymer are functional groups present at the ends of the main chain or side chains of each polymer, and functional groups present in the main chain or side chain. Functional groups include -CF=CF2, -CF2H, -COF, -COOH, -COOCH3, -CONH2, and -CH2OH.

[0036] The number of functional groups may be the total number of -CF=CF2, -CF2H, -COF, -COOH, -COOCH3, -CONH2, and -CH2OH.

[0037] The functional group is introduced, for example, by a chain transfer agent or a polymerization initiator used in producing the first perfluoropolymer and the second fluoropolymer, or by polymerizing a monomer having a functional group, the functional group is introduced into the side chain terminal of the polymer.

[0038] By subjecting the polymer having a functional group to a fluorination treatment, the first perfluoropolymer and the second fluoropolymer each having a main chain carbon number of 10 6 The total number of functional groups per polymer can be less than 100. That is, the composition of the present disclosure is preferably a composition containing a polymer that has been subjected to a fluorination treatment.

[0039] The composition of the present disclosure may be in the form of particles, a powder composition containing a plurality of particles, or a liquid composition. When the composition of the present disclosure is a liquid composition, the composition of the present disclosure may be a dispersion in which the particles are dispersed in water or an organic solvent. When the composition of the present disclosure is in the form of particles, the particles are preferably particles (hereinafter also referred to as "the present particles") that contain a first perfluoropolymer and a second fluoropolymer and have a PAVE unit content of 0.1 to 10.0 mol% relative to the total content of all structural units of the first perfluoropolymer and the second fluoropolymer.

[0040] When the composition of the present disclosure is a powder composition or a liquid composition, it preferably contains the present particles. The average particle size of the present particles is preferably 1 μm or less, more preferably 700 nm or less, and even more preferably 500 nm or less. From the viewpoint of aggregation, the lower limit of the average particle size of the present particles is preferably 30 nm. The composition of the present disclosure may be in the form of pellets or may be in the form of a molded article such as a film or a tube.

[0041] When the composition of the present disclosure is a particle or powder composition, the average particle size of the present particles means the arithmetic mean value of the particle sizes of five different particles obtained by photographing the present particles with a scanning electron microscope and determining the particle sizes from the resulting SEM image. When the composition of the present disclosure is a liquid composition, the average particle diameter of the present particles is determined by measuring the particle size distribution by a laser diffraction / scattering method, determining a cumulative curve with the total volume of the particle population set to 100%, and measuring the particle diameter (D50) at the point on the cumulative curve where the cumulative volume is 50%.

[0042] When the composition of the present disclosure is in the form of a dispersion, the viscosity of the dispersion is preferably 0.8 to 2.0 mPa·s, and more preferably 1.0 to 1.5 mPa·s, from the viewpoint of ease of handling. The viscosity of the dispersion is measured using a Brookfield viscometer at room temperature (25°C) and a rotation speed of 30 rpm. The measurement is repeated three times, and the average value of the three measurements is used.

[0043] The composition of the present disclosure is preferably substantially free of a fluorine-containing emulsifier, the details of which are described below. The composition of the present disclosure does not contain a fluorine-containing emulsifier, or the content of the fluorine-containing emulsifier is preferably 100 ppm by mass or less, more preferably 10 ppm by mass or less, even more preferably 5 ppm by mass or less, and particularly preferably 1 ppm by mass or less, relative to the total content of the first perfluoropolymer and the second fluoropolymer. The content of the fluorine-containing emulsifier relative to the total content of the first perfluoropolymer and the second fluoropolymer can be determined by a method similar to the method for measuring the content of the fluorine-containing surfactant by liquid chromatography-mass spectrometry described in paragraphs

[0364] to

[0369] of WO 2021 / 045227.

[0044] In the composition of the present disclosure, the content of the compound represented by the following formula (S1) relative to the total content of the first perfluoropolymer and the second fluoropolymer is preferably 1 ppb by mass or more, and more preferably 10 ppb by mass or more, relative to the fluoropolymer, from the viewpoint of processability.

[0045] In the composition of the present disclosure, the content of the compound represented by the following formula (S1) relative to the total content of the first perfluoropolymer and the second fluoropolymer is preferably 10,000 mass ppb or less, more preferably 1,000 mass ppb or less, and even more preferably 200 mass ppb or less, from the viewpoint of suppressing deterioration of the physical properties such as heat resistance of the composition of the present disclosure.

[0046] In the composition of the present disclosure, the content of the compound represented by the following formula (S2) relative to the total content of the first perfluoropolymer and the second fluoropolymer is preferably 0.1 ppb by mass or more, and more preferably 1 ppb by mass or more, relative to the fluoropolymer, from the viewpoint of processability.

[0047] In the composition of the present disclosure, the content of the compound represented by the following formula (S2) relative to the total content of the first perfluoropolymer and the second fluoropolymer is preferably 50 mass ppb or less, more preferably 25 mass ppb or less, from the viewpoint of suppressing deterioration of the physical properties such as heat resistance of the composition of the present disclosure. Formula (S1):H-(CF2) n -COOM Formula (S2):H-(CF2) m -SO3M In formula (S1) and formula (S2), M each independently represents a hydrogen atom, Na, K, or NH4; n represents 7 to 11; and m represents 8 to 12.

[0048] The content of the compound represented by formula (S1) relative to the total content of the first perfluoropolymer and the second fluoropolymer can be calculated by a method using an aqueous dispersion, among the measurement methods using a liquid chromatograph mass spectrometer described in paragraphs

[0710] to

[0720] of WO 2018 / 181904.

[0049] The content of the compound represented by formula (S2) relative to the total content of the first perfluoropolymer and the second fluoropolymer can be calculated by a method using an aqueous dispersion, among the measurement methods using a liquid chromatograph mass spectrometer described in paragraphs

[0721] to

[0732] of WO 2018 / 181904.

[0050] The composition of the present disclosure may be subjected to a fluorination treatment to adjust the content of the compound represented by formula (S1). Examples of the fluorination treatment method include the methods described below. Fluorination of the composition of the present disclosure can reduce the content of the compound represented by formula (S1) in the particles of the present disclosure.

[0051] [Method of producing fluorine-containing polymer] The method for producing a fluoropolymer of the present disclosure comprises the steps of preparing an aqueous dispersion A containing a first perfluoropolymer having a Tg of 10°C or less and an aqueous medium, and polymerizing a monomer containing TFE and HFP (hereinafter also referred to as a "specific monomer") in the aqueous dispersion A to produce a second fluoropolymer different from the first perfluoropolymer. Before starting polymerization of the specific monomer, the content of the first perfluoropolymer is 0.01 to 4.0 mass% based on the total mass of the aqueous dispersion A, and before starting polymerization of the specific monomer, the aqueous dispersion A does not contain a fluorinated emulsifier, or the content of the fluorinated emulsifier is 100 ppm by mass or less based on the total mass of the aqueous dispersion A.

[0052] In the present disclosure, "before initiating polymerization of the specific monomer" means immediately before the initiation of polymerization of the specific monomer. Here, examples of "initiation of polymerization" include the time when the specific monomer and the polymerization initiator are brought into the reactor after the temperature inside the reactor is raised to the polymerization temperature or higher, and the time when the temperature inside the reactor is raised to the polymerization temperature or higher after the temperature inside the reactor is raised to the polymerization temperature or higher.

[0053] In the method for producing a fluoropolymer of the present disclosure, by polymerizing a monomer containing TFE and HFP in an aqueous dispersion A containing a first perfluoropolymer having a Tg of 10°C or less and an aqueous medium, a second fluoropolymer can be produced efficiently even when the content of the fluorinated emulsifier is 100 ppm by mass or less relative to the total mass of the aqueous dispersion A.

[0054] The method for producing a fluoropolymer of the present disclosure preferably comprises, in this order, a step of preparing aqueous dispersion A and a step of producing a second fluoropolymer different from the first perfluoropolymer.

[0055] <Aqueous dispersion A preparation process> The method for producing a fluoropolymer of the present disclosure includes a step of preparing an aqueous dispersion A containing a first perfluoropolymer having a Tg of 10°C or lower and an aqueous medium (hereinafter also referred to as the "aqueous dispersion A preparation step").

[0056] (First perfluoropolymer) The details of the first perfluoropolymer having a Tg of 10° C. or less contained in the aqueous dispersion A prepared in the aqueous dispersion A preparation step are as described above.

[0057] The first perfluoropolymer is preferably dispersed in the aqueous medium in the form of particles. The average particle size of the first perfluoropolymer is preferably from 1 to 200 nm, more preferably from 10 to 150 nm, and even more preferably from 30 to 120 nm, from the viewpoint of more efficient production of the second fluoropolymer.

[0058] The average particle diameter of the first perfluoropolymer is determined by measuring the particle size distribution by a laser diffraction / scattering method, calculating a cumulative curve with the total volume of the particle group set as 100%, and determining the particle diameter (D50) at the point on the cumulative curve where the cumulative volume is 50%.

[0059] The first perfluoropolymer can be produced, for example, by polymerizing a monomer (preferably a mixture of monomers containing TFE and HFP) in a polymerization solvent in the presence of a polymerization initiator, thereby obtaining a dispersion of the first perfluoropolymer dispersed in particulate form in the polymerization solvent.

[0060] When polymerizing monomers to obtain a first perfluoropolymer, the pH of the reaction system containing the monomers and the polymerization solvent before the start of polymerization is preferably 6.5 or more, more preferably 7.0 or more, from the viewpoint of efficiently proceeding with the polymerization. The pH of the reaction system is preferably 10.5 or less, more preferably 10 or less, from the viewpoint of improving the stability of the first perfluoropolymer. The pH of the reaction system can be adjusted using a pH adjuster, such as the pH adjuster that may be contained in the aqueous dispersion A described below and ammonia, with ammonia being preferred.

[0061] The dispersion of the first perfluoropolymer thus obtained may be used as is as the aqueous dispersion A. Another aqueous medium may be added to the dispersion of the first perfluoropolymer, and the resulting mixture may be used as the aqueous dispersion. Alternatively, the first perfluoropolymer may be dispersed in another aqueous medium by solvent substitution, and the resulting mixture may be used as the aqueous dispersion A.

[0062] The polymerization initiator used in producing the first perfluoropolymer is preferably a water-soluble polymerization initiator, more preferably a persulfate such as ammonium persulfate, sodium persulfate, or potassium persulfate; a peroxide such as disuccinic acid peroxide; or an azo compound such as azobisisobutylamidine dihydrochloride, still more preferably a persulfate, and particularly preferably ammonium persulfate.

[0063] The polymerization solvent may be water or a mixed solvent of water and a water-soluble organic solvent, such as tert-butanol, propylene glycol, dipropylene glycol, dipropylene glycol monomethyl ether, or tripropylene glycol.

[0064] The method for producing the first perfluoropolymer may include a heating step of heating the dispersion liquid in which the first perfluoropolymer is dispersed after the dispersion liquid is obtained.

[0065] (aqueous medium) The aqueous medium contained in the aqueous dispersion A prepared in the aqueous dispersion A preparation step may be the polymerization solvent used in producing the first perfluoropolymer. Specific examples of the aqueous medium contained in the aqueous dispersion A are the same as the specific examples of the polymerization solvent used in producing the first perfluoropolymer. Before starting polymerization of the monomers used in the polymerization of the second perfluoropolymer, the content of the aqueous medium is preferably 60.0 to 99.9 mass%, more preferably 96.0 to 99.9 mass%, and even more preferably 98.0 to 99.9 mass%, relative to the total mass of the aqueous dispersion A.

[0066] (Other ingredients) The aqueous dispersion A may contain other components in addition to the first perfluoropolymer and the aqueous medium. Specific examples of other components that the aqueous dispersion A may contain include a chain transfer agent, an emulsifier other than the fluorine-containing emulsifier, a pH adjuster, and a wax.

[0067] In the present disclosure, an emulsifier is a compound that has a hydrophilic portion and a hydrophobic portion.

[0068] Examples of emulsifiers include hydrocarbon-containing surfactants, fluorine-containing emulsifiers, and polymer emulsifiers. Neither the first perfluoropolymer nor the second fluoropolymer falls under the category of an emulsifier. The emulsifier may be either ionic or non-ionic.

[0069] A hydrocarbon-containing surfactant is a surfactant containing a hydrocarbon group. More specifically, as long as the hydrocarbon-containing surfactant contains a hydrocarbon group, it may be substituted with a halogen atom such as a fluorine atom or a chlorine atom. In the hydrocarbon-containing surfactant, preferably 75% or more of the atoms or monovalent groups bonded to the carbon atoms of the hydrocarbon group are hydrogen atoms, more preferably 85% or more, and even more preferably 95% or more.

[0070] The hydrocarbon-containing surfactants include hydrocarbon surfactants and siloxane surfactants.The hydrocarbon surfactants refer to surfactants that do not contain silicon atoms, and 100% of the atoms or monovalent groups bonded to the carbon atoms of the hydrocarbon group are hydrogen atoms, so they do not contain halogen atoms such as chlorine atoms and fluorine atoms.The siloxane surfactants refer to hydrocarbon-containing surfactants that have a hydrophobic group and a siloxane skeleton containing many siloxane units.

[0071] Hydrocarbon surfactants include anionic hydrocarbon surfactants. An anionic hydrocarbon surfactant refers to a hydrocarbon surfactant having a negatively charged hydrophilic portion such as a carboxylic acid group, sulfonic acid group, sulfate group, phosphonic acid group, or phosphate group, and a hydrocarbon portion such as an alkyl group as a hydrophobic portion. An example of an anionic hydrocarbon surfactant is the highly branched C10 tertiary carboxylic acid supplied by Resolution Performance Products as Versatic® 10. Other examples of anionic hydrocarbon surfactants include the sodium linear alkyl polyether sulfonates supplied by BASF as their Avanel® S series.

[0072] Anionic hydrocarbon surfactants also include sodium dodecyl sulfate.

[0073] Another example of an anionic hydrocarbon surfactant is the sulfosuccinate surfactant Lankropol® K8300, available from Akzo Nobel Surface Chemistry LLC.

[0074] Hydrocarbon surfactants also include nonionic hydrocarbon surfactants. Nonionic hydrocarbon surfactants do not have charged groups, but have a hydrophobic portion, which is often a long hydrocarbon chain.The hydrophilic portion of nonionic hydrocarbon surfactants includes water-soluble functional groups, such as polyethylene oxide chains obtained from the polymerization of ethylene oxide.Nonionic hydrocarbon surfactants include block copolymers with various types of polyalkylene oxide blocks, such as polyethylene oxide and polypropylene oxide.

[0075] Examples of the nonionic hydrocarbon surfactant include surfactants described in paragraphs

[0043] to

[0052] of JP-A No. 2016-537499.

[0076] Siloxane surfactants include those described in US Pat. Nos. 6,841,616 (Wille et al.) and 7,977,438 (Brothers et al.).

[0077] The fluorine-containing emulsifier may be an anionic fluorine-containing surfactant. Examples of anionic fluorine-containing surfactants include surfactants containing fluorine atoms in which the total number of carbon atoms excluding the anionic group is 20 or less, and surfactants containing fluorine in the anionic moiety having a molecular weight of 800 or less. The "anionic moiety" refers to the moiety excluding the cation of the fluorine-containing surfactant.

[0078] The polymer emulsifier may be a water-soluble polymer having a hydrophilic group in its side chain. Such a polymer emulsifier may be, for example, a polymer containing a structural unit based on a compound having a site capable of polymerization reaction and a hydrophilic group. Further, a polymer obtained by subjecting a polymer containing a structural unit based on a compound having a group that can become a hydrophilic group to post-treatment such as hydrolysis may also be used.

[0079] Specific examples of the chain transfer agent include ethyl acetate, methanol, ethanol, t-butyl methyl ether, diethyl ether, n-pentane, cyclohexane, methane, and propane. From the viewpoint of being able to control the molecular weight with a small amount, the chain transfer agent is preferably t-butyl methyl ether or methane, and more preferably t-butyl methyl ether.

[0080] Specific examples of pH adjusters include inorganic salts. Specific examples of inorganic salts include phosphates such as disodium hydrogen phosphate and sodium dihydrogen phosphate; and carbonates such as sodium bicarbonate and sodium carbonate. More preferred specific examples of phosphates include disodium hydrogen phosphate dihydrate and disodium hydrogen phosphate dodecahydrate.

[0081] Specific examples of waxes include Parafffin Wax-155 and Parafffin Wax-150 (both manufactured by Nippon Seiro Co., Ltd.).

[0082] When the aqueous dispersion A contains a chain transfer agent, the content of the chain transfer agent is preferably 0.1 to 5.0 parts by mass relative to 100 parts by mass of the aqueous medium. The amount is preferably 0.1 to 20.0 parts by mass, more preferably 0.1 to 15.0 parts by mass, and even more preferably 0.1 to 10.0 parts by mass, relative to 100 parts by mass of the used amount of the fixed monomer. When the aqueous dispersion A contains an emulsifier other than the fluorine-containing emulsifier, the content of the emulsifier other than the fluorine-containing emulsifier is preferably 0.01 to 5.0 parts by mass relative to 100 parts by mass of the aqueous medium.

[0083] When the aqueous dispersion A contains a pH adjuster, the content of the pH adjuster is preferably 0.01 to 3.0 parts by mass relative to 100 parts by mass of the aqueous medium.

[0084] The pH of aqueous dispersion A is preferably 1.0 or more, more preferably 2.0 or more, from the viewpoint of stable polymerization of the second fluoropolymer, and is preferably 11 or less, more preferably 10.5 or less, from the viewpoint of stable polymerization of the second fluoropolymer. When the aqueous dispersion A contains a wax, the content of the wax is preferably 1 to 10 parts by mass relative to 100 parts by mass of the aqueous medium.

[0085] From the viewpoint of stably polymerizing the second fluoropolymer, the viscosity of aqueous dispersion A is preferably 2.0 mPa·s or less, more preferably 1.9 mPa·s or less, and even more preferably 1.7 mPa·s or less. From the viewpoint of stably polymerizing the second fluoropolymer, the viscosity of aqueous dispersion A is preferably 0.85 mPa·s or more, and more preferably 0.9 mPa·s or more.

[0086] The thixotropy ratio of aqueous dispersion A is preferably 0.9 or more, more preferably 0.95 or more, from the viewpoint of stable polymerization of the second fluoropolymer, and is preferably 1.2 or less, more preferably 1.1 or less, from the viewpoint of stable polymerization of the second fluoropolymer. The viscosity of aqueous dispersion A is measured using a Brookfield viscometer at room temperature (25°C) and a rotation speed of 30 rpm. The measurement is repeated three times, and the average value of the three measurements is used. The thixotropy ratio of aqueous dispersion A is the value obtained by dividing the viscosity of aqueous dispersion A measured at a rotation speed of 30 rpm by the viscosity of aqueous dispersion A measured at a rotation speed of 60 rpm.

[0087] <Second fluoropolymer manufacturing process> The method for producing a fluoropolymer of the present disclosure includes a step of polymerizing a specific monomer in aqueous dispersion A to produce a second fluoropolymer different from the first perfluoropolymer (hereinafter also referred to as the "second fluoropolymer production step").

[0088] Details of the second fluoropolymer are as described above.

[0089] Before the start of polymerization of the specific monomer, the content of the first perfluoropolymer is 0.01 to 4.0 mass%, preferably 0.05 to 3.0 mass%, and more preferably 0.1 to 2.0 mass%, relative to the total mass of the aqueous dispersion A. When the content of the first perfluoropolymer is 0.01 mass% or more, the polymerization stability (productivity) is excellent, and when the content of the first perfluoropolymer is 4.0 mass% or less, the polymer obtained by polymerization (i.e., the mixture of the first perfluoropolymer and the second fluoropolymer) has excellent heat resistance.

[0090] Before the start of polymerization of the specific monomer, the aqueous dispersion A does not contain a fluorinated emulsifier, or the content of the fluorinated emulsifier is 100 ppm by mass or less, preferably 50 ppm by mass or less, more preferably 25 ppm by mass or less, and still more preferably 5 ppm by mass or less, relative to the total mass of the aqueous dispersion A. The lower limit is 0 ppm by mass. In the method for producing a fluoropolymer of the present disclosure, the second fluoropolymer can be produced efficiently even when the content of the fluorinated emulsifier is 100 ppm by mass or less.

[0091] Before starting polymerization of the specific monomer, the concentration of fluoride ions is preferably 100 ppm by mass or less, and more preferably 50 ppm by mass or less, based on the total mass of the aqueous dispersion A, from the viewpoint of polymerization stability. The lower limit is 0 ppm by mass. One example of a method for adjusting the fluoride ion concentration to the above range is to remove sulfate ions using an anion exchange resin during production of the first perfluoropolymer. Here, the fluoride ions may be generated by the reaction between a polymerization initiator (for example, ammonium persulfate) and the monomer used in producing the first fluorine-containing polymer, and may be contained in the aqueous dispersion.

[0092] Before the start of polymerization of the specific monomer, the concentration of sulfate ions is preferably 10 ppm by mass or less, more preferably 5 ppm by mass or less, relative to the total mass of the aqueous medium in the aqueous dispersion, from the viewpoint of suppressing coloration of the second fluorine-containing polymer. The lower limit is 0 ppm by mass.

[0093] An example of a method for adjusting the sulfate ion concentration to the above range is to remove sulfate ions using an anion exchange resin during production of the first perfluoropolymer.

[0094] Here, the sulfate ions are derived from, for example, a polymerization initiator (particularly, ammonium persulfate) used in producing the first perfluoropolymer, and may be contained in the aqueous dispersion containing the first perfluoropolymer. When the content of sulfate ions is 10 ppm by mass or less (particularly, 5 ppm by mass or less), It is presumed that by keeping the content of the fluoropolymer at a concentration of 1 ppm or less, it is possible to prevent end groups with low heat resistance from being formed in the second fluoropolymer, thereby preventing discoloration of the second fluoropolymer.

[0095] Before starting polymerization of the specific monomer, the concentration of ammonium ions is preferably 20 ppm by mass or less, more preferably 10 ppm by mass or less, relative to the total mass of the aqueous medium in the aqueous dispersion, in order to suppress aggregation of the second fluoropolymer.The lower limit is 0 ppm by mass.

[0096] One example of a method for adjusting the ammonium ion concentration to the above range is to remove ammonium ions using a cation exchange resin during the production of the first perfluoropolymer. Here, the ammonium ions are derived from, for example, an initiator (particularly ammonium persulfate) used in producing the first perfluoropolymer, and may be contained in the aqueous dispersion containing the first perfluoropolymer. It is presumed that by keeping the ammonium ion content at 20 mass ppm or less, the ionic strength in the aqueous medium decreases, thereby improving the production efficiency of the second fluoropolymer.

[0097] (Specific monomer) Specific monomers include TFE and HFP.

[0098] The amount of HFP used relative to the total amount of TFE and HFP used is preferably 1.0 to 15.0 mol %, more preferably 1.0 to 13.0 mol %, and even more preferably 1.0 to 11.0 mol %, from the viewpoint of heat resistance.

[0099] The specific monomer may contain other monomers in addition to TFE and HFP. From the viewpoint of heat resistance, the amount of the other monomers used is preferably 10.0 mol % or less, more preferably 5.0 mol % or less, based on the total amount of the specific monomers used. It is more preferable that the specific monomer does not substantially contain other monomers. "Substantially free of other monomers" means that the amount of other monomers used is 0.01 mol % or less, or may be 0.00 mol %, based on the total amount of the specific monomers used. Examples of other monomers include fluoroolefins such as PAVE (excluding TFE and HFP); and acid anhydrides such as itaconic anhydride, citraconic anhydride, and 5-norbornene-2,3-dicarboxylic anhydride.

[0100] The amount of the specific monomer used is preferably 1 to 50 parts by mass, more preferably 1 to 40 parts by mass, and even more preferably 1 to 30 parts by mass, relative to 100 parts by mass of the aqueous medium contained in the aqueous dispersion A.

[0101] (Polymerization initiator) In the second fluoropolymer production step, it is preferable to polymerize the specific monomer in the presence of a polymerization initiator.

[0102] The polymerization initiator is preferably an oil-soluble radical initiator, a water-soluble radical initiator, or a water-soluble oxidation-reduction catalyst.

[0103] Examples of oil-soluble radical initiators include oil-soluble organic peroxides such as tert-butyl peroxypivalate (hereinafter also referred to as "PBPV") and diisopropyl peroxydicarbonate (hereinafter also referred to as "IPP").

[0104] Examples of the water-soluble radical initiator include persulfates such as ammonium persulfate and potassium persulfate, and water-soluble organic peroxides such as disuccinic acid peroxide, bisglutaric acid peroxide, and tert-butyl hydroperoxide (hereinafter also referred to as "TBHP").

[0105] Preferred water-soluble redox catalysts are combinations of oxidizing agents such as bromic acid or its salts, chloric acid or its salts, persulfuric acid or its salts, permanganic acid or its salts, and hydrogen peroxide with reducing agents such as sulfurous acid or its salts, hydrogen sulfite or its salts, thiosulfuric acid or its salts, organic acids, and inorganic salts. Preferred persulfates are potassium persulfate and ammonium persulfate. Preferred sulfites are sodium sulfite. Examples of inorganic salts include combinations of sulfate anions, sulfite anions, and chloride anions with metal ions. Preferred metal ions are transition metal ions, including manganese, iron, cobalt, nickel, copper, zinc, cerium, and silver ions, with iron ions being preferred. Preferred inorganic salts are iron(II) sulfate.

[0106] The polymerization initiator is preferably an oil-soluble radical initiator or a water-soluble radical initiator, more preferably an oil-soluble radical initiator from the viewpoint of more efficiently producing a fluorine-containing polymer, and even more preferably an oil-soluble organic peroxide. The polymerization initiator may be used alone or in combination of two or more kinds.

[0107] The amount of the polymerization initiator used is preferably 1 to 1000 ppm by mass, more preferably 5 to 750 ppm, and even more preferably 10 to 500 ppm, relative to the amount of the specific monomer used.

[0108] (Other ingredients) When polymerizing the specific monomer, components other than those described above (hereinafter also referred to as "other components") may be further used. A specific example of the other components is a reducing agent. The amount of the other components used is preferably 1 to 2000 ppm by mass relative to the amount of the specific monomer used.

[0109] (Manufacturing method) The second fluoropolymer obtained in the second fluoropolymer production step may be copolymerized with the first perfluoropolymer.

[0110] The specific monomer is introduced into the reaction system (i.e., polymerization reaction vessel) by a conventional method. For example, the specific monomer may be introduced into the reaction system continuously or intermittently so that the polymerization pressure becomes a predetermined pressure. The specific monomer may be dissolved in an aqueous medium, and the resulting solution may be introduced into the reaction system continuously or intermittently. When a polymerization initiator is used, the polymerization initiator may be added to the reaction system all at once or in portions.

[0111] The polymerization temperature is preferably from 10 to 95°C, more preferably from 15 to 90°C. The polymerization pressure is preferably from 0.5 to 4.0 MPaG, more preferably from 0.6 to 3.5 MPaG. In the case of batch processing, the polymerization time is preferably from 90 to 1000 minutes, more preferably from 90 to 700 minutes.

[0112] When the first perfluoropolymer is in particulate form, it is presumed that the specific monomer polymerizes within or near the particles of the first perfluoropolymer during polymerization of the specific monomer, and therefore it is believed that the method for producing a fluorinated polymer of the present disclosure produces particles containing the first perfluoropolymer and the second fluoropolymer. That is, it is presumed that the second fluoropolymer is obtained in the form of particles containing the first perfluoropolymer and the second fluoropolymer. In this case, an aqueous dispersion is obtained in which particles containing the first perfluoropolymer and the second fluoropolymer are dispersed in the above-mentioned aqueous medium.

[0113] In the method for producing a fluoropolymer of the present disclosure, it is preferable to obtain particles containing a first perfluoropolymer and a second fluoropolymer. That is, the method for producing a fluoropolymer of the present disclosure comprises: A step of preparing an aqueous dispersion A containing particles of a first perfluoropolymer having a glass transition temperature of 10°C or less and an aqueous medium; a step of polymerizing a monomer containing tetrafluoroethylene and a perfluoro(alkyl vinyl ether) in an aqueous dispersion A to produce particles containing a first perfluoropolymer and a second fluoropolymer different from the first perfluoropolymer; before the start of polymerization of the monomers, the content of the first perfluoropolymer is 0.01 to 4.0% by mass relative to the total mass of the aqueous dispersion A; In the method for producing a fluorinated polymer, it is preferable that, before the start of polymerization of the monomers, the aqueous dispersion A does not contain a fluorinated emulsifier, or the content of the fluorinated emulsifier in the aqueous dispersion A is 100 ppm by mass or less, based on the total mass of the aqueous dispersion A. From the viewpoint of polymerization stability, the average particle size of the particles containing the first perfluoropolymer and the second fluoropolymer is preferably 1 μm or less, more preferably 700 nm or less, and more preferably 500 nm or less. From the viewpoint of aggregation, the lower limit of the average particle size of the particles containing the first perfluoropolymer and the second fluoropolymer is preferably 30 nm.

[0114] In the production method for a fluoropolymer of the present disclosure, the average particle size of particles is determined by measuring the particle size distribution by a laser diffraction / scattering method, determining a cumulative curve with the total volume of the particle population set to 100%, and determining the particle size at the point on the cumulative curve where the cumulative volume is 50%.

[0115] When the first perfluoropolymer is in particulate form and particles containing the first perfluoropolymer and the second fluoropolymer are obtained by the method for producing a fluoropolymer of the present disclosure, the ratio of the average particle size of the particles containing the first perfluoropolymer and the second fluoropolymer to the average particle size of the particles of the first perfluoropolymer is preferably at least 2, more preferably at least 3. From the viewpoint of polymerization stability, the ratio of the average particle sizes is preferably at most 10, more preferably at most 8. When the ratio is at least 2, particles having excellent heat resistance that reflect the physical properties of the second fluoropolymer can be obtained.

[0116] <Fluorination process> The method for producing a fluoropolymer of the present disclosure preferably further comprises a step of subjecting the first perfluoropolymer and the second fluoropolymer to a fluorination treatment (hereinafter also referred to as a "fluorination step").

[0117] The method of fluorination treatment is not particularly limited, and can be carried out by a conventionally known method. For example, fluorination can be carried out by contacting the first perfluoropolymer and the second fluoropolymer with fluorine gas. The fluorine gas may be diluted with an inert gas before use. Examples of inert gases include rare gases such as helium gas, neon gas, and argon gas, and nitrogen gas, with nitrogen gas or helium gas being preferred, and nitrogen gas being more preferred from the viewpoint of economical advantages. The proportion of fluorine gas is preferably 10 to 60% by volume, with the total of fluorine gas and inert gas being 100% by volume.

[0118] The temperature for the fluorination treatment is, for example, 100 to 250°C. The fluorination treatment time is, for example, 1 to 15 hours.

[0119] By carrying out the fluorination step, the functional groups contained in the first perfluoropolymer and the second fluoropolymer are fluorinated, which improves the heat resistance. The first perfluoropolymer and the second fluoropolymer each have a main chain carbon number of 10 6 The total number of functional groups per unit is preferably less than 100, more preferably 50 or less, and even more preferably 30 or less. The lower limit of the number of functional groups is 0.

[0120] [Aqueous dispersion] The aqueous dispersion of the present disclosure is an aqueous dispersion comprising an aqueous medium and melt-moldable particles, wherein the particles have an average particle size of 1 μm or less, the particles comprise one or more fluoropolymers, the fluoropolymers comprise TFE units, PAVE units, and HFP units, the content of PAVE units is 0.1 to 5.0 mol% based on all constituent units of the fluoropolymer, the content of particles is 1 to 50 mass% based on the total mass of the aqueous dispersion, and the aqueous dispersion does not contain a fluorinated emulsifier or the content of the fluorinated emulsifier is 100 ppm by mass or less based on the content of the fluorinated polymer.

[0121] The aqueous dispersion of the present disclosure can be obtained, for example, by the method for producing the fluoropolymer of the present disclosure. The above aqueous dispersion A is an aqueous dispersion obtained during the process for producing a fluoropolymer of the present disclosure, and is different from the aqueous dispersion of the present disclosure.

[0122] <Melt-moldable particles> The aqueous dispersions of the present disclosure comprise melt-formable particles.

[0123] In the present disclosure, "melt-moldable" means that the melt flow rate (MFR) is 0.1 to 1000 g / 10 min. The MFR of the particles is preferably 0.1 to 100 g / 10 min, more preferably 1 to 80 g / 10 min. In the present disclosure, MFR is measured in accordance with ASTM D3307 under conditions of a temperature of 372°C and a load of 49 N, and is measured as the mass flowing through an orifice having a diameter of 2 mm and a length of 8 mm in 10 minutes.

[0124] The average particle size of the particles is 1 μm or less, and from the viewpoint of dispersibility, it is preferably 700 nm or less, more preferably 500 nm or less. From the viewpoint of aggregation, the lower limit of the average particle size of the particles is preferably 30 nm.

[0125] In the present disclosure, the average particle size of particles is determined by measuring the particle size distribution by a laser diffraction / scattering method, calculating a cumulative curve with the total volume of the particle group set as 100%, and determining the particle size at the point on the cumulative curve where the cumulative volume is 50%.

[0126] From the viewpoint of dispersion stability, the content of the particles is 1 to 50 mass % relative to the total mass of the aqueous dispersion of the present disclosure, preferably 2 to 45 mass %, and more preferably 3 to 40 mass %.

[0127] The particles contained in the aqueous dispersion of the present disclosure contain one or more fluorine-containing polymers. The fluorine-containing polymer contains TFE units, PAVE units, and HFP units.

[0128] When the particles contain two or more types of fluoropolymers, the particles are only required to contain a fluoropolymer containing TFE units, PAVE units, and HFP units, and may also contain a fluoropolymer that does not fall under the category of fluoropolymers containing TFE units, PAVE units, and HFP units.

[0129] When the particles contain two or more kinds of fluoropolymers, one fluoropolymer does not have to contain all of the TFE unit, PAVE unit, and HFP unit. For example, the particles may contain a fluoropolymer containing TFE units and PAVE units, and a fluoropolymer containing TFE units and HFP units.

[0130] The content of HFP units relative to the total content of TFE units and HFP units is preferably from 1.0 to 15.0 mol %, more preferably from 1.0 to 13.0 mol %, and even more preferably from 1.0 to 11.0 mol %, from the viewpoint of heat resistance.

[0131] Furthermore, when the particles contain two or more types of fluoropolymers, any one of the fluoropolymers contained in the particles may not be melt-formable, so long as the particles are melt-formable.

[0132] The content of PAVE units is 0.1 to 5.0 mol%, preferably 0.1 to 4.0 mol%, more preferably 0.1 to 3.0 mol%, based on all constitutional units of the fluoropolymer. Since the content of PAVE units is 0.1 to 5.0 mol%, the heat resistance is excellent.

[0133] When the particles contain two or more types of fluoropolymers, "all structural units of the fluoropolymer" means all structural units in the two or more types of fluoropolymers.

[0134] In the PAVE unit, the PAVE is preferably a monomer represented by the above formula (1).

[0135] Among them, PAVE is preferably PMVE because of its superior heat resistance.

[0136] The particles preferably contain the first perfluoropolymer and the second fluoropolymer, details of which are as described above.

[0137] The content of the first perfluoropolymer in the particles is preferably 0.01% by mass or more, more preferably 0.1% by mass or more. The content of the first perfluoropolymer in the particles is preferably 10% by mass or less, more preferably 5% by mass or less.

[0138] The content of the second fluoropolymer in the particles is preferably 90% by mass or more, more preferably 95% by mass or more. The content of the second fluoropolymer in the particles is preferably 99.99% by mass or less, more preferably 99.9% by mass or less.

[0139] The ratio of the content of the first perfluoropolymer to the total content of the first perfluoropolymer and the second fluoropolymer in the particles is preferably 0.01% by mass or more, more preferably 0.1% by mass or more, from the viewpoint of improving physical properties such as heat resistance. The content ratio of the first perfluoropolymer to the total content of the first perfluoropolymer and the second fluoropolymer in the particles is preferably 10% by mass or less, more preferably 5% by mass or less, from the viewpoint of improving physical properties such as heat resistance.

[0140] <Aqueous medium> Specific examples of the aqueous medium contained in the aqueous dispersion of the present disclosure are the same as the specific examples of the aqueous medium used in producing the first perfluoropolymer described above.

[0141] The content of the aqueous medium is preferably 50 to 99 mass %, more preferably 60 to 99 mass %, and even more preferably 70 to 99 mass %, relative to the total mass of the aqueous dispersion of the present disclosure.

[0142] <Other> The aqueous dispersion of the present disclosure is preferably substantially free of a fluorine-containing emulsifier, the details of which are as described above. The aqueous dispersion of the present disclosure does not contain a fluorine-containing emulsifier, or the content of the fluorine-containing emulsifier is 100 ppm by mass or less, preferably 10 ppm by mass or less, more preferably 5 ppm by mass or less, and even more preferably 1 ppm by mass or less, relative to the content of the fluorine-containing polymer. The content of the fluorinated emulsifier relative to the content of the fluorinated polymer can be determined by a method similar to the method for measuring the content of the fluorinated surfactant by liquid chromatography-mass spectrometry described in paragraphs

[0364] to

[0369] of WO 2021 / 045227.

[0143] From the viewpoint of processability, the viscosity of the aqueous dispersion of the present disclosure is preferably 0.8 to 2.0 mPa·s, and more preferably 1.0 to 1.5 mPa·s. The viscosity of the aqueous dispersion is measured using a Brookfield viscometer at room temperature (25°C) and a rotation speed of 30 rpm. The measurement is repeated three times, and the average value of the three measurements is used.

[0144] In the aqueous dispersion of the present disclosure, the content of the compound represented by the following formula (S1) relative to the fluoropolymer is preferably 1 ppb by mass or more, and more preferably 10 ppb by mass or more, relative to the fluoropolymer, from the viewpoint of stabilizing the fluoropolymer in the aqueous dispersion. In the aqueous dispersion of the present disclosure, the content of the compound represented by the following formula (S1) relative to the fluoropolymer is preferably 10,000 ppb by mass or less, more preferably 1,000 ppb by mass or less, and even more preferably 200 ppb by mass or less, from the viewpoint of preventing deterioration of physical properties.

[0145] In the aqueous dispersion of the present disclosure, the content of the compound represented by the following formula (S2) relative to the fluoropolymer is preferably 0.1 ppb by mass or more, and more preferably 1 ppb by mass or more, relative to the fluoropolymer, from the viewpoint of stabilizing the fluoropolymer in the aqueous dispersion. In the aqueous dispersion of the present disclosure, the content of the compound represented by the following formula (S2) relative to the fluoropolymer is preferably 50 ppb by mass or less, more preferably 25 ppb by mass or less, from the viewpoint of preventing deterioration of physical properties. Formula (S1):H-(CF2) n -COOM Formula (S2):H-(CF2) m -SO3M In formula (S1) and formula (S2), M each independently represents a hydrogen atom, Na, K, or NH4; n represents 7 to 11; and m represents 8 to 12.

[0146] The content of the compound represented by formula (S1) in the fluoropolymer can be calculated by a method using an aqueous dispersion, among the measurement methods using a liquid chromatograph mass spectrometer described in paragraphs

[0710] to

[0720] of WO 2018 / 181904.

[0147] The content of the compound represented by formula (S2) in the fluoropolymer can be calculated by a method using an aqueous dispersion, among the measurement methods using a liquid chromatograph mass spectrometer described in paragraphs

[0721] to

[0732] of WO 2018 / 181904.

[0148] The compound represented by formula (S1) and the compound represented by formula (S2) are components that can be generated when the above-mentioned specific monomer (particularly TFE) is polymerized in the presence of a polymerization initiator, a chain transfer agent, and a fluorinated emulsifier. Therefore, in the method for producing a fluorinated polymer of the present disclosure, when a fluorinated emulsifier is not used, the amounts of the compound represented by formula (S1) and the compound represented by formula (S2) generated can be suppressed, and it is easy to keep the contents of these compounds within the above ranges.

[0149] <Application> As described above, the aqueous dispersion of the present disclosure does not necessarily require a fluorine-containing emulsifier, and therefore can easily be made into a dispersion in an organic solvent such as N-methylpyrrolidone or acetone by solvent substitution. For example, the aqueous dispersion of the present disclosure can be mixed with an organic solvent and dehydrated using evaporation or anhydrous sodium sulfate or the like to form a dispersion in an organic solvent.

[0150] In the aqueous dispersion of the present disclosure, the fluorine-containing polymer is stably dispersed even without containing a fluorine-containing emulsifier, and therefore, it can be suitably used for coating applications, binders, etc.

[0151] Additionally, powders can be obtained by agglomerating particles from the aqueous dispersion of the present disclosure.

[0152] The aggregation method includes, but is not limited to, freeze aggregation, acid aggregation, base aggregation, and aggregation using a coagulant. In the case of freeze aggregation, the aggregation temperature is preferably −20 to 0° C. The aggregation time is preferably 1 hour or more, more preferably 2 hours or more. In the case of acid coagulation, a method of adding an acid-containing solution to the aqueous dispersion of the present disclosure is preferred. Examples of the acid to be added include hydrochloric acid, nitric acid, sulfuric acid, oxalic acid, and hydrofluoric acid, with hydrochloric acid being preferred. The concentration of the acid in the acid-containing solution is preferably 0.1 to 50% by mass, more preferably 1 to 30% by mass, and even more preferably 1 to 10% by mass. A preferred method for base coagulation is to add a solution containing a base to the aqueous dispersion of the present disclosure. Examples of the base to be added include sodium hydroxide, potassium hydroxide, and ammonium carbonate, with sodium hydroxide being preferred. The concentration of the base in the solution containing the base is preferably 0.1 to 50% by mass, more preferably 1 to 30% by mass, and even more preferably 1 to 10% by mass. For aggregation using a coagulant, known coagulants can be used. Known coagulants include aluminum salts, calcium salts, and magnesium salts. Specific examples include aluminum sulfate, alum represented by the general formula M'Al(SO4)2·12H2O (where M' is a monovalent cation other than lithium), calcium nitrate, and magnesium sulfate. Alum is preferred, and potassium alum, where M is potassium, is more preferred. As the aggregation method, base aggregation is preferred because aggregation is particularly likely to proceed.

[0153] [particle] The particles of the present disclosure are melt-formable particles, The average particle size of the particles is 1 μm or less, the particles contain one or more fluorine-containing polymers, the fluorine-containing polymer contains TFE units, PAVE units, and HFP units; the content of PAVE units is 0.1 to 5.0 mol% based on the total structural units of the fluorine-containing polymer, does not contain a fluorine-containing emulsifier, or the content of the fluorine-containing emulsifier is 100 ppm by mass or less relative to the content of the fluorine-containing polymer, The content of (S1) is 1 to 10,000 ppb by mass, and the content of (S2) is 100 ppb by mass or less, relative to the fluorine-containing polymer. Formula (S1):H-(CF2) n -COOM Formula (S2):H-(CF2) m -SO3M In formula (S1) and formula (S2), M each independently represents a hydrogen atom, Na, K, or NH4; n represents 7 to 11; and m represents 8 to 12. The particles of the present disclosure can be obtained, for example, by the method for producing a fluoropolymer of the present disclosure. Alternatively, the particles of the present disclosure may be obtained by aggregating particles from the aqueous dispersion of the present disclosure.

[0154] <Melt-moldable particles> The definition of melt-processible particles in the particles of the present disclosure, including preferred embodiments and ranges thereof, is the same as that in the aqueous dispersion of the present disclosure. However, for the particles of the present disclosure, the average particle size of the particles means the arithmetic mean value of the particle sizes of five different particles obtained by photographing the particles with a scanning electron microscope and determining the particle sizes from the resulting SEM image.

[0155] <Other> The particles of the present disclosure are preferably substantially free of a fluorine-containing emulsifier, the details of which are as described above. The particles of the present disclosure do not contain a fluorine-containing emulsifier, or the content of the fluorine-containing emulsifier is 100 ppm by mass or less, preferably 10 ppm by mass or less, more preferably 5 ppm by mass or less, and even more preferably 1 ppm by mass or less, relative to the content of the fluorine-containing polymer. The content of the fluorinated emulsifier relative to the content of the fluorinated polymer can be determined by a method similar to the method for measuring the content of the fluorinated surfactant by liquid chromatography-mass spectrometry described in paragraphs

[0364] to

[0369] of WO 2021 / 045227.

[0156] The particles of the present disclosure have a content of the compound represented by formula (S1) of 1 to 10,000 ppb by mass and a content of the compound represented by formula (S2) of 100 ppb by mass or less, relative to the fluoropolymer. The compound represented by formula (S1) and the compound represented by formula (S2) are components that can be generated when the above-mentioned specific monomer (particularly TFE) is polymerized in the presence of a polymerization initiator, a chain transfer agent, and an emulsifier. Therefore, in the method for producing a fluorinated polymer of the present disclosure, when no emulsifier is used, the amounts of the compound represented by formula (S1) and the compound represented by formula (S2) generated can be suppressed, and it is easy to keep the contents of these compounds within the above ranges.

[0157] In the particles of the present disclosure, the content of the compound represented by formula (S1) relative to the fluoropolymer is preferably 10 ppb by mass or more relative to the fluoropolymer, from the viewpoint of processability. In the particles of the present disclosure, the content of the compound represented by formula (S1) relative to the fluoropolymer is preferably 1000 ppb by mass or less, more preferably 200 ppb by mass or less, from the viewpoint of suppressing deterioration of physical properties such as heat resistance.

[0158] In the particles of the present disclosure, the content of the compound represented by formula (S2) relative to the fluoropolymer is preferably 0.1 ppb by mass or more, more preferably 1 ppb by mass or more, relative to the fluoropolymer, from the viewpoint of processability. In the particles of the present disclosure, the content of the compound represented by formula (S2) relative to the fluoropolymer is preferably 50 ppb by mass or less, more preferably 25 ppb by mass or less, from the viewpoint of suppressing deterioration of physical properties such as heat resistance.

[0159] The content of the compound represented by formula (S1) in the fluoropolymer can be calculated by a method using a powder, among the measurement methods using a liquid chromatograph mass spectrometer described in paragraphs

[0710] to

[0720] of WO 2018 / 181904.

[0160] The content of the compound represented by formula (S2) in the fluoropolymer can be calculated by a method using a powder, among the measurement methods using a liquid chromatograph mass spectrometer described in paragraphs

[0721] to

[0732] of WO 2018 / 181904.

[0161] The particles of the present disclosure may be further subjected to a fluorination treatment to adjust the content of the compound represented by formula (S1). Examples of the fluorination treatment method include the methods described above. By fluorinating the particles of the present disclosure, the content of the compound represented by formula (S1) in the particles of the present disclosure can be reduced.

[0162] In addition, the fluorine-containing polymer of the particles of the present disclosure has a main chain carbon number of 10 6 The total number of functional groups per unit is preferably less than 100, more preferably 50 or less, and even more preferably 30 or less. The lower limit of the number of functional groups is 0. Examples of the functional group include those mentioned above, and the method for measuring the number of functional groups is also as mentioned above. <Application> Since the particles of the present disclosure are substantially free of emulsifiers, they can easily be made into a dispersion in an organic solvent such as N-methylpyrrolidone or acetone. The particles of the present disclosure may be used in a powder composition. [Example]

[0163] The present invention will be described in detail below with reference to examples. Example 1 is an embodiment, and Examples 2 and 3 are comparative examples. However, the present invention is not limited to these examples.

[0164] [Measurement and evaluation methods] The various measurement and evaluation methods are as follows.

[0165] <Glass transition temperature (Tg)> Tg was measured using a NEXTA DSC600 manufactured by Hitachi High-Technologies Corporation. Specifically, 5 mg of the sample for measurement was weighed into an aluminum sample pan, and the sample was heated to 100°C at a heating rate of 10°C / min under a nitrogen atmosphere. It was then cooled to -60°C at a rate of 10°C / min. Once the specified temperature was reached, the temperature was again raised to 100°C at 10°C / min. Tg was estimated from the inflection point observed during this second heating operation.

[0166] <Average particle size of particles in liquid> The raw material liquid was degassed for 5 minutes at room temperature (25°C), pressurized with nitrogen to 0.2 MPaG, and then purged to atmospheric pressure to obtain a sample for measurement. The particle size of the obtained sample was measured using a laser diffraction / scattering particle size distribution analyzer (Otsuka Electronics Co., Ltd., ELSZ) with an accumulation count set to 100 and measurement started. D50 was calculated from the particle diameters measured in the range of 1 to 300 nm, and this was used as the average particle size of the particles in the raw material liquid. The average particle size of the particles in the aqueous dispersion corresponding to the raw material liquid was measured in the same manner as for the raw material liquid, and was found to be the same as that of the particles in the raw material liquid. Here, the aqueous dispersion corresponding to the raw material liquid means aqueous dispersion A1 corresponding to raw material liquid T2 in Example 1 described later. The average particle size (D50) of particles in each aqueous dispersion obtained using an aqueous dispersion corresponding to the raw material liquid was measured using a laser diffraction / scattering particle size analyzer (ELSZ, Otsuka Electronics Co., Ltd.). However, the range of particle sizes to be measured was not limited, unlike the method for measuring the average particle size of particles in the raw material liquid. Here, the aqueous dispersion obtained using an aqueous dispersion corresponding to the raw material liquid in each example means aqueous dispersion 1 obtained using aqueous dispersion A1 in the case of Example 1 described below.

[0167] <Average particle size after drying> The aqueous dispersion containing the second fluoropolymer obtained in each example was coagulated, filtered, and then dried to obtain particles, which were then photographed using a scanning electron microscope (e.g., JSM-IT700HR InTouchScope, manufactured by JEOL Ltd.) The particle sizes of five different particles measured from the obtained SEM images were determined and then the arithmetic mean was calculated.

[0168] <Proportion of each structural unit in the polymer> The proportion of each structural unit in the polymer was determined by 19F-NMR analysis and infrared absorption spectroscopy.

[0169] <Fluorine-containing emulsifier content> The content of the fluorinated emulsifier relative to the content of the fluorinated polymer was determined by a method similar to the method for measuring the content of the fluorinated surfactant by liquid chromatography-mass spectrometry described in paragraphs

[0364] to

[0369] of WO 2021 / 045227.

[0170] <Content of the compound represented by formula (S1)> The content of the compound represented by formula (S1) relative to the content of the fluoropolymer was calculated by a method using an aqueous dispersion or a powder composition, among the measurement methods using a liquid chromatograph mass spectrometer described in paragraphs

[0710] to

[0720] of WO 2018 / 181904. The instrument used was an Agilent 1260 Series HPLC / 6460S, and the column used was an Imtakt Cadenza CD-C18.

[0171] <Content of the compound represented by formula (S2)> The content of the compound represented by formula (S2) relative to the content of the fluoropolymer was calculated by a method using an aqueous dispersion or a powder composition, among the measurement methods using a liquid chromatograph mass spectrometer described in paragraphs

[0721] to

[0732] of WO 2018 / 181904. The instrument used was an Agilent 1260 Series HPLC / 6460S, and the column used was an Imtakt Cadenza CD-C18.

[0172] [Production of raw material solution T1] Ultrapure water (717 g), PMVE (50 g), and TFE (8 g) were charged into a 1.3 L stainless steel pressure reactor and heated to 90°C while stirring at 500 rpm. Next, an aqueous solution of ammonium persulfate (3.6 mass%, 5 mL) was added to initiate polymerization. As the polymerization began, the pressure inside the reactor decreased, so TFE was added to maintain the pressure constant. When 1 g of TFE had been injected, the reactor was cooled to terminate the polymerization reaction. The gas remaining in the reactor was recovered, and the liquid was then withdrawn. This liquid was designated raw material liquid T1. The raw material liquid T1 was freeze-aggregated and then filtered. The resulting fluoropolymer 1A was analyzed by NMR, and the ratio of TFE units to PMVE units was 52 / 48 (molar ratio) and Tg was -5.9°C.

[0173] [Production of raw material solution T2] To the above raw material solution T1 (490 g) was added Dowex Monosphere 650C (manufactured by DuPont, cation exchange resin, 20 g). 60 minutes after starting stirring, the raw material solution was separated from the ion exchange resin by filtration. To the filtered raw material solution, Purolite A300 (manufactured by Purolite, anion exchange resin, 20 g) was added. 60 minutes after starting stirring, the raw material solution was separated from the ion exchange resin by filtration, and raw material solution T2 was obtained. In raw material liquid T2, particles of fluoropolymer 1A (average particle size 52 nm) were dispersed in an aqueous medium, and the content of fluoropolymer 1A was 0.4 mass % relative to the total mass of raw material liquid T2.

[0174] <Example 1> A 1.0 L stainless steel pressure reactor was charged with ultrapure water (149 g), raw material solution T2 (475 g), and t-BuOMe (0.5 g) to obtain aqueous dispersion A1. The pH of aqueous dispersion A1 was 4.7, the viscosity was 1.1 mPa·s, and the thixotropy ratio was 1.0. Aqueous dispersion A1 was heated to 63°C while stirring at 260 rpm. Next, HFP (16 g) was charged, and TFE was injected into the reactor until the reactor pressure reached 1.0 MPaG. An aqueous solution of ammonium persulfate (APS) (0.5 wt%, 5 mL) was added to initiate polymerization. As the polymerization began, the pressure in the reactor decreased, so TFE was added to maintain the pressure constant. After 100 g of TFE was injected, the reactor was cooled and the polymerization reaction was terminated. The polymerization time was 560 minutes. The gas remaining in the reactor was recovered, and the liquid was then withdrawn. This liquid was designated as aqueous dispersion 1. Aqueous dispersion 1 was a dispersion in which particles (average particle diameter 220 nm) containing fluoropolymer 1A were dispersed in an aqueous medium, and had a solids concentration of 15.0 mass%, a pH of 2.0, and a viscosity of 1.4 mPa·s. The obtained particles contained a first perfluoropolymer containing TFE units and PMVE units and a second fluoropolymer containing TFE units and HFP units within the same particle. The ratio of the average particle size of the obtained particles to the average particle size of the particles of fluoropolymer 1A contained in raw material liquid T2 was 4.2. Aqueous dispersion 1 had a fluorinated emulsifier content of less than 25 ppb by mass relative to the total content of the first perfluoropolymer and the second fluoropolymer. The resulting particles were aggregated and dried to obtain Particles 1 (average particle diameter 211 nm). The composition of Particles 1 was calculated using NMR, and the molar ratio was TFE unit / HFP unit / PMVE unit = 95.4 / 3.8 / 0.8. The MFR was 12.7 g / 10 min. Particle 1 contained a first perfluoropolymer containing TFE units and PMVE units and a second fluoropolymer containing TFE units and HFP units within the same particle, and the content of the first perfluoropolymer was 98.3% by mass, and the content of the second fluoropolymer was 1.7% by mass. The content of the fluorine-containing emulsifier in the particles 1 was less than 25 ppb by mass relative to the total content of the first perfluoropolymer and the second fluoropolymer. In particle 1, the content of the compound represented by the above formula (S1) was 120 ppb by mass, and the content of the compound represented by the above formula (S2) was less than 25 ppb by mass, relative to the total content of the first perfluoropolymer and the second fluoropolymer.

[0175] <Example 2> A 1.0 L stainless steel pressure reactor was charged with ultrapure water (624 g) and t-BuOMe (0.5 g) to obtain aqueous dispersion C. Aqueous dispersion C was heated to 63 °C while stirring at 260 rpm. Next, HFP (16 g) was charged, and TFE was injected into the reactor until the pressure reached 1.0 MPaG. An aqueous APS solution (0.5 wt%, 5 mL) was added to initiate polymerization. As the polymerization began, the pressure in the reactor decreased, so TFE was added to maintain the pressure constant. After 40 g of TFE had been injected, the reactor was cooled and the polymerization reaction was terminated. The polymerization time was 520 minutes. After recovering the gas remaining in the reactor, the liquid was extracted, but all of it had aggregated, and it was not possible to obtain an aqueous dispersion in which fluoropolymer particles were dispersed in an aqueous medium.

[0176] <Example 3> A 1.0 L stainless steel pressure reactor was charged with ultrapure water (608 g), a fluorine-containing emulsifier (ammonium salt of C2F5OCF2CF2OCF2COOH, 30% by mass, 16 g), and t-BuOMe (0.5 g) to obtain aqueous dispersion D. Aqueous dispersion D was heated to 63 °C while stirring at 260 rpm. Next, HFP (16 g) was charged, and TFE was injected into the reactor until the reactor pressure reached 1.0 MPaG. An aqueous APS solution (0.5% by mass, 5 mL) was added to initiate polymerization. As the polymerization began, the pressure in the reactor decreased, so TFE was added to maintain the pressure constant. After 100 g of TFE had been injected, the reactor was cooled and the polymerization reaction was terminated. The polymerization time was 180 minutes. After collecting the gas remaining in the reactor, the liquid was extracted. This liquid was designated as aqueous dispersion 3. Aqueous dispersion 3 had a solids concentration of 15.6% by mass. The obtained particles were aggregated and dried to obtain particles 3. The composition of particles 3 was calculated using NMR, and the molar ratio was TFE unit / FEP unit = 95.4 / 4.6. The MFR was 1.1 g / 10 min. In particles 3, the content of the fluorine-containing emulsifier was 2200 ppb by mass relative to the content of the fluorine-containing polymer having TFE units and FEP units. In particles 3, the content of the compound represented by the above formula (S1) was 300 ppb by mass, and the content of the compound represented by the above formula (S2) was less than 25 ppb by mass, relative to the content of the fluoropolymer having TFE units and FEP units.

[0177] [evaluation] (Fluorination treatment) Particles 1 and 3 were placed in a vacuum oscillatory reactor and heated to 210°C. After evacuation, fluorine gas diluted to 20% by volume with nitrogen gas was introduced. After 2 hours, the atmosphere inside the reactor was thoroughly replaced with nitrogen gas to terminate the fluorination reaction. The fluorinated particles were analyzed, and the number of terminal functional groups was calculated.

[0178] (Main chain carbon number 10 6 (number of functional groups per unit) Fluorinated particles 1 and 3 were each press-molded at 340°C to produce a 200 μm thick film. This film was scanned 16 times using a Fourier transform infrared spectrometer and analyzed to obtain an infrared absorption spectrum. Fluorinated particles 1 and 3 were placed in a vacuum oscillatory reactor and heated to 210°C. After evacuation, fluorine gas diluted to 20% by volume with nitrogen gas was introduced. After 10 hours, the reactor was thoroughly purged with nitrogen gas to terminate the fluorination reaction, yielding fully fluorinated particles 1 and 3. Fully fluorinated particles 1 and 3 were each press-molded at 340°C to produce a 200 μm thick perfluorinated film. The perfluorinated film was scanned 16 times using a Fourier transform infrared spectrometer and analyzed to obtain a base spectrum. From the absorption peaks of specific functional groups appearing in the difference spectrum between the obtained infrared absorption spectrum and the base spectrum, the fluorinated particles 1 and 3 having 10 carbon atoms in the main chain were determined according to the following formula (A). 6 The number of functional groups per molecule, N, was calculated. N=I×K / t …(A) I: Absorbance K: Correction coefficient t: film thickness (mm)

[0179] Table 2 shows the absorption frequency, molar absorption coefficient, and correction factor for specific functional groups such as -CF2H. The molar absorption coefficient of a specific functional group is determined from FT-IR measurement data of a low molecular weight model compound.

[0180] [Table 2]

[0181] In the copolymers, the absorption frequencies of -CH2CF2H, -CH2COF, -CH2COOH, -CH2COOCH3 and -CH2CONH2 are calculated by multiplying the absorption frequencies of -CF2H, -COF, -COOH (free and bonded), -COOCH3 and -CONH2 shown in the table by several tens of Kaiser (cm -1 ) becomes lower. For example, the number of -COF is the absorption frequency of 1883 cm due to -CF2COF. -1 The number of functional groups determined from the absorption peak of -CH2COF and the absorption frequency of 1840 cm -1 The number of functional groups is the sum of the number of functional groups determined from the absorption peaks of the

[0182] (Heat resistance) 2 g of each of the fluorinated particles 1 and 3 was weighed out and heated for 2 hours at 340° C. The degree of foaming of the sample after heating was visually observed.

[0183] The fluorinated particles 1 are composed of a first perfluoropolymer and a second fluoropolymer each having 10 carbon atoms in the main chain. 6 The number of functional groups per molecule was less than 10. The fluorinated particles 3 are made of a fluorine-containing polymer having a main chain carbon number of 10 and a TFE unit and an FEP unit. 6 The number of functional groups per molecule was less than 10. Furthermore, it was found that none of the fluorinated particles foamed when heated and had excellent heat resistance.

[0184] From the above, it was found that in Example 1, a fluorinated copolymer having excellent heat resistance equivalent to that of Example 3 was obtained without using a fluorinated emulsifier. In Example 2, a fluorine-containing polymer could not be obtained without using a fluorine-containing emulsifier.

[0185] The composition of the present disclosure can be obtained without using a fluorine-containing emulsifier, and is extremely useful in cases where the use of a fluorine-containing emulsifier is restricted.

[0186] The disclosures of Japanese Patent Application No. 2023-129556, filed on August 8, 2023, and Japanese Patent Application No. 2024-099099, filed on June 19, 2024, are incorporated herein by reference in their entirety. In addition, all documents, patent applications, and technical standards described herein are incorporated herein by reference to the same extent as if each individual document, patent application, and technical standard were specifically and individually indicated to be incorporated by reference.

Claims

1. a first perfluoropolymer having a glass transition temperature of 10°C or less; a second fluoropolymer that contains structural units based on tetrafluoroethylene and structural units based on hexafluoropropylene and is different from the first perfluoropolymer; A composition in which the content of structural units based on perfluoro(alkyl vinyl ether) is 0.1 to 5.0 mol % relative to the total content of all structural units of the first perfluoropolymer and the second fluoropolymer.

2. Neither the first perfluoropolymer nor the second fluoropolymer contains a functional group, or the first perfluoropolymer and the second fluoropolymer each have a main chain carbon number of 10 or less. ６ The composition according to claim 1 , wherein the total number of functional groups per unit is less than 100.

3. 3. The composition of claim 1 or 2, wherein the first perfluoropolymer comprises constitutional units based on tetrafluoroethylene and constitutional units based on perfluoro(alkyl vinyl ether).

4. The composition according to claim 3, wherein the first perfluoropolymer contains 20 to 70 mol% of structural units based on perfluoro(alkyl vinyl ether) relative to the total of structural units based on tetrafluoroethylene and structural units based on perfluoro(alkyl vinyl ether).

5. A step of preparing an aqueous dispersion A containing a first perfluoropolymer having a glass transition temperature of 10°C or less and an aqueous medium; and polymerizing, in the aqueous dispersion A, monomers including tetrafluoroethylene and hexafluoropropylene to produce a second fluoropolymer different from the first perfluoropolymer, before starting polymerization of the monomer, the content of the first perfluoropolymer is 0.01 to 4.0% by mass relative to the total mass of the aqueous dispersion A; the aqueous dispersion A does not contain a fluorinated emulsifier, or the content of the fluorinated emulsifier in the aqueous dispersion A is 100 ppm by mass or less, based on the total mass of the aqueous dispersion A, before polymerization of the monomers is started.

6. The process for producing a fluorinated polymer according to claim 5, wherein the amount of the monomer used is 1 to 50 parts by mass per 100 parts by mass of the aqueous medium used.

7. the step of preparing the aqueous dispersion A is a step of preparing an aqueous dispersion A containing particles of the first perfluoropolymer and an aqueous medium, the step of producing the second fluoropolymer is a step of polymerizing the monomer to produce a second fluoropolymer different from the first perfluoropolymer, and producing particles containing the first perfluoropolymer and the second fluoropolymer; 7. The method for producing a fluoropolymer according to claim 5 or 6, wherein the ratio of the average particle size of particles containing the first perfluoropolymer and the second fluoropolymer to the average particle size of particles of the first perfluoropolymer is 2 or more.

8. The process for producing a fluoropolymer according to claim 5 or 6, wherein the viscosity of the aqueous dispersion A is 2.0 mPa·s or less.

9. The process for producing a fluoropolymer according to claim 5 or 6, wherein the thixotropy ratio of said aqueous dispersion A is from 0.9 to 1.

2.

10. The process for producing a fluorine-containing polymer according to claim 5 or 6, wherein the monomers are polymerized in the presence of a polymerization initiator.

11. The method for producing a fluoropolymer according to claim 5 or 6, further comprising a step of subjecting the first perfluoropolymer and the second fluoropolymer to a fluorination treatment.

12. An aqueous dispersion comprising an aqueous medium and melt-formable particles, The particles have an average particle size of 1 μm or less, the particles contain one or more fluorine-containing polymers, the fluorine-containing polymer contains a structural unit based on tetrafluoroethylene, a structural unit based on perfluoro(alkyl vinyl ether), and a structural unit based on hexafluoropropylene, the content of the structural units based on the perfluoro(alkyl vinyl ether) is 0.1 to 5.0 mol % based on all structural units of the fluorine-containing polymer, the content of the particles is 1 to 50% by mass based on the total mass of the aqueous dispersion, An aqueous dispersion which does not contain a fluorine-containing emulsifier or has a fluorine-containing emulsifier content of 100 ppm by mass or less relative to the content of the fluorine-containing polymer.

13. The aqueous dispersion according to claim 12, having a viscosity of 0.8 to 2.0 mPa·s.

14. 1. A melt-formable particle comprising: The particles have an average particle size of 1 μm or less, the particles contain one or more fluorine-containing polymers, the fluorine-containing polymer contains a structural unit based on tetrafluoroethylene, a structural unit based on perfluoro(alkyl vinyl ether), and a structural unit based on hexafluoropropylene, the content of the structural units based on the perfluoro(alkyl vinyl ether) is 0.1 to 5.0 mol % based on all structural units of the fluorine-containing polymer, does not contain a fluorine-containing emulsifier, or the content of the fluorine-containing emulsifier is 100 ppm by mass or less relative to the content of the fluorine-containing polymer, Particles, wherein the content of the compound represented by formula (S1) is 1 to 10,000 ppb by mass, and the content of the compound represented by formula (S2) is 100 ppb by mass or less, relative to the fluoropolymer. Formula (S1): H-(CF) ２ ) ｎ -COM Formula (S2): H-(CF ２ ) ｍ -SO ３ M In formula (S1) and formula (S2), M each independently represents a hydrogen atom, Na, K, or NH ４ wherein n is 7 to 11, and m is 8 to 12.

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