Oil-resistant agent composition

Abstract

This oil-resistant agent composition contains (1) a hydrocarbon-containing polymer having a long-chain hydrocarbon group, and (2) a crosslinking agent component. As a result, the oil-resistant agent composition can impart oil resistance to a base material (for example, fiber or paper).

Description

Oil-resistant composition 【0001】 This disclosure relates to an oil-resistant composition. 【0002】 Patent Document 1 discloses an oil-resistant agent for paper comprising (a) a repeating unit formed from an acrylic monomer having a long-chain hydrocarbon, and (b) a non-fluorinated copolymer having a repeating unit formed from an acrylic monomer having a hydrophilic group. The oil-resistant agent for paper described in Patent Document 1 can impart oil resistance to paper, but higher oil resistance is required. 【0003】 International Patent Application Publication No. 2020-054856 【0004】 The purpose of this disclosure is to provide a novel oil-resistant composition that can impart oil resistance to a substrate (e.g., fibers, paper). 【0005】 The disclosure includes the following embodiments: [Claim 1] An oil-resistant composition comprising (1) a hydrocarbon-containing polymer having long-chain hydrocarbon groups, and (2) a crosslinking agent component. [Claim 2] The oil-resistant composition according to Claim 1, wherein the crosslinking agent component is at least one selected from the group consisting of aldehyde compounds, organometallic compounds, isocyanate compounds, and epoxy compounds. [Claim 3] The oil-resistant composition according to Claim 2, wherein the aldehyde compound is a glyoxal compound. [Claim 4] The oil-resistant composition according to any one of Claims 1 to 3, comprising a water-soluble polymer. [Claim 5] The oil-resistant composition according to Claim 4, wherein the water-soluble polymer is a polyol. [Claim 6] The oil-resistant composition according to Claim 5, wherein the polyol is at least one selected from the group consisting of polysaccharides and polyvinyl alcohol. [Clause 7] The oil-resistant composition according to any one of Claims 1 to 6, wherein the hydrocarbon-containing polymer (1) comprises repeating units derived from a monomer (a) having 7 to 40 hydrocarbon groups, and repeating units derived from a hydrophilic group-containing monomer (b). [Clause 8] The monomer (a) is of the formula: CH2=C(-X ａ )-C(=O)-Y ａ (R ａ ) ｋ [In the formula, R ａ Each of these is independently a hydrocarbon group having 7 to 40 carbon atoms, and X ａis a hydrogen atom, a monovalent organic group or a halogen atom, and Y ａ is a divalent to tetravalent hydrocarbon group having 1 carbon atom, -C ６ H ４ -, -O-, -C(=O)-, -S(=O) ２ -, or a group composed of at least one selected from -NH-, and k is 1 to 3. ] The oil-resistant agent composition according to Item 7. [Item 9] The monomer (b) has the formula: CH ２ =CX ｂ C(=O)-Y ｂ -(R ｂ O) ｎ -A ｂ [In the formula, X ｂ is a hydrogen atom or a methyl group, Y ｂ is -O- or -NH-, R ｂ are each independently an alkylene group having 2 to 6 carbon atoms, A ｂ is a hydrogen atom, an unsaturated or saturated hydrocarbon group having 1 to 22 carbon atoms, or CH ２ =CX ｂ[Claim 10] The oil-resistant composition according to claim 7 or 8, represented by C(=O)-, where n is an integer from 1 to 90. [Claim 11] The oil-resistant composition according to any one of claims 1 to 9, wherein the (1) hydrocarbon-containing polymer comprises an ionic group-containing monomer (c). [Claim 12] The oil-resistant composition according to any one of claims 1 to 11, wherein the amount of the (2) crosslinking agent component is 10% by weight or more and 55% by weight or less with respect to the total amount of the (1) hydrocarbon-containing polymer and the (2) crosslinking agent component. [Claim 13] The oil-resistant composition according to any one of claims 1 to 11, wherein the (1) hydrocarbon-containing polymer comprises repeating units derived from a monomer (a) having a hydrocarbon group having 7 to 40 carbon atoms, and repeating units derived from a hydrophilic group-containing monomer (b), and the (2) crosslinking agent component is a glyoxal compound and comprises a polysaccharide. [Claim 13] An oil-resistant composition according to any one of claims 1 to 12, for use in pulp products. [Claim 14] A pulp product comprising (1) a hydrocarbon-containing polymer having long-chain hydrocarbon groups, and (2) a crosslinking agent component, in the oil-resistant composition according to any one of claims 1 to 13. [Claim 15] A pulp product according to claim 14, which is oil-resistant paper or water-resistant paper. [Claim 16] A pulp product according to claim 14 or 15, which is food packaging material or food container. 【0006】 The oil-resistant compositions described herein can impart good liquid repellency (particularly oil resistance) to paper products. 【0007】 <Oil-resistant composition> The oil-resistant composition in this disclosure comprises (1) a hydrocarbon-containing polymer and (2) a crosslinking agent component. The oil-resistant composition may also contain other components. 【0008】 The oil-resistant compositions in this disclosure impart oil resistance to substrates (e.g., fibrous substrates, paper substrates). The oil-resistant compositions may also function as at least one selected from the group consisting of water-repellent agents, oil-repellent agents, and water-resistant agents. By using the oil-resistant compositions in this disclosure, oil resistance can be imparted without excessively increasing the air permeability of the treated paper, making them useful for applications where air permeability is required (e.g., food packaging paper for packaging oil-cooked chicken or potatoes, freshness-preserving sheets, etc.). 【0009】Other examples of applications for the oil-resistant compositions in this disclosure include external treatment agents (surface treatment agents) or internal treatment agents, water repellents (water repellents, oil repellents or water- and oil-repellent agents, etc., especially water repellents), antifouling agents, dirt removal agents, release agents, mold release agents (external mold release agents or internal mold release agents), and the like. 【0010】 The oil-repellent compositions in this disclosure do not necessarily contain any one selected from the group consisting of compounds having 8 or more carbon atoms in a fluoroalkyl group, compounds having 8 or more carbon atoms in a perfluoroalkyl group, compounds having 4 or more carbon atoms in a fluoroalkyl group, compounds having 4 or more carbon atoms in a perfluoroalkyl group, compounds having a perfluoroalkyl group, compounds having a fluoroalkyl group, and compounds having a fluorine atom. The oil-repellent compositions in this disclosure can impart water-repellent and oil-repellent properties to a substrate even without containing these fluorine compounds. 【0011】 [(1) Hydrocarbon-containing polymer] Hydrocarbon-containing polymer (1) is a polymer obtained by polymerizing vinyl monomers and exhibits liquid repellency. Here, the vinyl monomer may be any compound having a polymerizable carbon-carbon double bond (ethylenically unsaturated double bond) (>C=C<), and may be a monomer containing a vinyl group, vinylene group, vinylidene group, acryloyl group, methacryloyl group, or derivative groups thereof. Typically, hydrocarbon-containing polymer (1) is an acrylic polymer having repeating units derived from (meth)acrylic monomers. 【0012】The hydrocarbon-containing polymer (1) has long-chain hydrocarbon groups. Specifically, the hydrocarbon-containing polymer (1) has monovalent hydrocarbon groups having 7 to 40 carbon atoms. The hydrocarbon groups may be aromatic hydrocarbon groups or aliphatic hydrocarbon groups, and aliphatic hydrocarbon groups, particularly saturated aliphatic hydrocarbon groups (alkyl groups), are preferred. The hydrocarbon groups are branched or linear, and more preferably linear. The hydrocarbon groups may be saturated or unsaturated. The hydrocarbon groups are preferably saturated aliphatic hydrocarbon groups (alkyl groups). The number of carbon atoms in the hydrocarbon group may be 7 or more, 8 or more, 10 or more, 12 or more, 14 or more, 16 or more, 18 or more, 20 or more, or 22 or more, preferably 10 or more, 12 or more, or 16 or more, and may also be 40 or less, 35 or less, 30 or less, 25 or less, 20 or less, 15 or less, or 10 or less, preferably 30 or less, 25 or less, or 20 or less. 【0013】 The HD (n-hexadecane) contact angle of the hydrocarbon-containing polymer (1) may be 10° or more, 15° or more, 25° or more, 35° or more, 55° or more, 55° or more, or 65° or more, preferably 30° or more, and may also be 100° or less, 90° or less, or 75° or less. By having an HD contact angle of the hydrocarbon-containing polymer (1) above the lower limit, good liquid repellency (especially oil repellency and oil resistance) can be imparted to the substrate. The HD contact angle is the static contact angle of the hydrocarbon-containing polymer (1) with respect to the spin-coated film, as shown in the examples, and is obtained by dropping 2 μL of HD onto the spin-coated film and measuring the contact angle 1 second after dropping. 【0014】The water contact angle of the hydrocarbon-containing polymer (1) may be 35° or more, 40° or more, 45° or more, 50° or more, 55° or more, 65° or more, 75° or more, 85° or more, 90° or more, or 100° or more, and may also be 160° or less, 140° or less, 130° or less, 120° or less, 110° or less, 100° or less, or 90° or less. By having a water contact angle of the hydrocarbon-containing polymer (1) above the lower limit, good liquid repellency (especially water repellency and water resistance) can be imparted to the substrate. The water contact angle is the static contact angle of the hydrocarbon-containing polymer (1) with respect to the spin-coated film, as shown in the examples, and is obtained by dropping 2 μL of water onto the spin-coated film and measuring the contact angle 1 second after the drop. 【0015】 The hydrocarbon-containing polymer (1) is preferably a compound having carbon of bio-based origin. The degree of bio-basedness is measured in accordance with ASTM D6866. The degree of bio-basedness may be 20% or more, preferably 30% or more, more preferably 50% or more, even more preferably 60% or more, even more preferably 70% or more, most preferably 80% or more or 90% or more, for example 100%. A high degree of bio-basedness means that the amount of fossil resource-based materials represented by petroleum etc. is small, and from this viewpoint, a higher degree of bio-basedness of the hydrocarbon-containing polymer (1) is preferable. 【0016】 The hydrocarbon-containing polymer (1) in this disclosure does not necessarily have to contain any of the group selected from the group consisting of a fluoroalkyl group having 8 or more carbon atoms, a perfluoroalkyl group having 8 or more carbon atoms, a fluoroalkyl group having 4 or more carbon atoms, a perfluoroalkyl group having 4 or more carbon atoms, a perfluoroalkyl group, a fluoroalkyl group, and a fluorine atom. Even if the long-chain hydrocarbon-containing polymer (1) does not contain these fluorine-containing groups, it can still impart oil resistance to the substrate. 【0017】The weight-average molecular weight of the hydrocarbon-containing polymer (1) may be 3,000 or more, 5,000 or more, 10,000 or more, 30,000 or more, 100,000 or more, 300,000 or more, or 500,000 or more, and may also be 1,000,000 or less, 750,000 or less, 500,000 or less, 300,000 or less, 100,000 or less, 75,000 or less, 50,000 or less, 30,000 or less, 10,000 or less, or 5,000 or less. 【0018】 The melting point or glass transition point (e.g., melting point) of the hydrocarbon-containing polymer (1) may be 20°C or higher, 30°C or higher, 35°C or higher, 40°C or higher, 45°C or higher, 50°C or higher, or 55°C or higher, and may also be 200°C or lower, 150°C or lower, 100°C or lower, 80°C or lower, or 70°C or lower. 【0019】 The hydrocarbon-containing polymer (1) has repeating units derived from a monomer (a) having a hydrocarbon group with 7 to 40 carbon atoms. In addition to the repeating units derived from monomer (a), the hydrocarbon-containing polymer (1) may have (b) a monomer having a hydrophilic group, (c) an ionic group-containing monomer, and / or (d) repeating units derived from other monomers. In particular, it is preferable that the hydrocarbon-containing polymer (1) has repeating units formed from (b) a monomer having a hydrophilic group. Furthermore, it is preferable that the hydrocarbon-containing polymer (1) has repeating units formed from (c) an ionic group-containing monomer, in addition to monomers (a) and (b). In addition to monomers (a), (b), and (c), the hydrocarbon-containing polymer (1) may have (d) repeating units formed from other monomers. 【0020】 [(a) Hydrocarbon group-containing monomer] The hydrocarbon-containing polymer (1) has repeating units derived from monomer (a) having a hydrocarbon group with 7 to 40 carbon atoms. Monomer (a) may be a monomer. 【0021】The hydrocarbon group of monomer (a) may be an aromatic hydrocarbon group or an aliphatic hydrocarbon group, and is preferably an aliphatic hydrocarbon group, particularly a saturated aliphatic hydrocarbon group (alkyl group). The hydrocarbon group may be branched or linear, and is more preferably linear. The hydrocarbon group may be saturated or unsaturated. The hydrocarbon group is preferably a saturated aliphatic hydrocarbon group (alkyl group). The number of carbon atoms in the hydrocarbon group may be 7 or more, 8 or more, 10 or more, 12 or more, 14 or more, 16 or more, 18 or more, 20 or more, or 22 or more, and is preferably 10 or more, 12 or more, 14 or more, or 16 or more, and may also be 40 or less, 35 or less, 30 or less, 25 or less, 20 or less, 15 or less, or 10 or less, and is preferably 30 or less, 25 or less, or 20 or less. 【0022】 Monomer (a) may contain an amide group, a urea group, or a urethane group. The hydrocarbon monomer may be a combination of a hydrocarbon monomer having an amide group, a urea group, or a urethane group and a hydrocarbon monomer not having an amide group, a urea group, or a urethane group. The effects of this disclosure can be favorably achieved by including such groups in monomer (a). 【0023】 A monomer (a) having a hydrocarbon group with 7 to 40 carbon atoms is given by the formula: CH2=C(-X ａ )-C(=O)-Y ａ (R ａ ) ｋ [In the formula, R ａ Each of these is independently a hydrocarbon group having 7 to 40 carbon atoms, and X ａ Y is a hydrogen atom, a monovalent organic group, or a halogen atom. ａ This refers to divalent to tetravalent hydrocarbon groups with one carbon atom (especially -CH ２ -, -CH=), -C ６ H ４ -, -O-, -C(=O)-, -S(=O) ２ It is preferably a monomer represented by ], which is a group consisting of at least one selected from - or -NH-, where k is 1 to 3. 【0024】 X ａThis may be a hydrogen atom, a methyl group, a halogen other than a fluorine atom, a substituted or unsubstituted benzyl group, or a substituted or unsubstituted phenyl group. ａ Examples include hydrogen atoms, methyl groups, chlorine atoms, bromine atoms, iodine atoms, and cyano groups. ａ It is preferable that the element is a hydrogen atom, a methyl group, or a chlorine atom. ａ It is particularly preferable that it be a hydrogen atom. 【0025】 Y ａ It is a divalent to tetravalent group. ａ It is preferable that the group is divalent. ａ This is a hydrocarbon group having 1 carbon atom, -C ６ H ４ -, -O-, -C(=O)-, -S(=O) ２ Preferably, the group is composed of at least one selected from - or -NH- (excluding hydrocarbon groups). An example of a C1 hydrocarbon group is -CH ２ Examples include -CH= with a branched structure or -C≡ with a branched structure. 【0026】 Y ａ -Y'-, -Y'-Y'-, -Y'-C(=O)-, -C(=O)-Y'-, -Y'-C(=O)-Y'-, -Y'-R'-, -Y'-R'-Y'- , -Y'-R'-Y'-C(=O)-, -Y'-R'-C(=O)-Y'-, -Y'-R'-Y'-C(=O)-Y'-, or -Y'-R'-Y'-R'- [In the formula, Y' is a direct bond, -O-, -NH- or -S(=O) ２ - and R' is - (CH ２ ) m - (m is an integer between 1 and 5) or -C ６ H ４ - (phenylene group). ] This may be the case. 【0027】 Y ａ Specific examples of are -O-, -NH-, -OC(=O)-, -C(=O)-NH-, -NH-C(=O)-, -OC(=O)-NH-, -NH-C(=O)-O-, -NH-C(=O)-NH-, -O-C ６ H ４ -, -O-(CH ２ )m -O-、-NHH-(CH ２ ) m -NHH-、-O-(CH ２ ) m -NHH-、-NHH-(CH ２ ) m -O-、-O-(CH ２ ) m -O-C(=O)-、-O-(CH ２ ) m -C(=O)-O-、-NHH-(CH ２ ) m -O-C(=O)-、-NH-(CH ２ ) m -C(=O)-O-、-O-(CH ２ ) m -O-C(=O)-NH-、-O-(CH ２ ) m -NHH-C(=O)-O-、-O-(CH ２ ) m -C(=O)-NH-、-O-(CH ２ ) m -NHH-C(=O)-、-O-(CH ２ ) m -NH-C(=0)-NH-,-O-(CH ２ ) m -O-C ６ H ４ -、-O-(CH ２ ) m -NHH-S(=O) ２ -、-O-(CH ２ ) m -S(=O) ２ -NHH-、-NHH-(CH ２ ) m -O-C(=O)-NH-、-NH-(CH ２ ) m -NH-C(=0)-O-、-NH-(CH ２ ) m -C(=0)-NH-、-NHH-(CH ２ ) m -NH-C(=0)-、-NH-(CH ２ ) m -NH-C(=0)-NH-, -NH-(CH ２ ) m -O-C ６ H４ -, -NH-(CH ２ ) m -NH-C ６ H ４ -, -NH-(CH ２ ) m -NH-S(=O) ２ -, or -NH-(CH ２ ) m -S(=O) ２ -NH- [wherein m is 1 to 5, especially 2 or 4]. 【0028】 Y ａ is -O-, -NH-, -O-(CH ２ ) m -O-C(=O)-, -O-(CH ２ ) m -NH-C(=O)-, -O-(CH ２ ) m -OC(=O)-NH-, -O-(CH ２ ) m -NH-C(=O)-O-, -O-(CH ２ ) m -NH-C(=O)-NH-, -O-(CH ２ ) m -NH-S(=O) ２ -, -O-(CH ２ ) m -S(=O) ２ -NH-, -NH-(CH ２ ) m -NH-S(=O) ２ -, or -NH-(CH ２ ) m -S(=O) ２ -NH- [wherein m is an integer from 1 to 5, particularly 2 or 4.] is preferable. Y ａ is -O- or -O-(CH ２ ) m -NH-C(=O)-, especially -O-(CH ２ ) m It is more preferable that it be -NH-C(=O)-. 【0029】 R ａThe hydrocarbon group is preferably a linear or branched hydrocarbon group. The hydrocarbon group may be a linear hydrocarbon group in particular. The hydrocarbon group is preferably an aliphatic hydrocarbon group, especially a saturated aliphatic hydrocarbon group, and especially an alkyl group. The number of carbon atoms in the hydrocarbon group is preferably 12 to 30, for example 16 to 26 or 15 to 26, and especially 18 to 22 or 17 to 22. 【0030】 An example of monomer (a) is given by equation (a1): CH2 = C(-X ａ１ ) - C (= O) - Y ａ１ -R ａ１ [In the formula, R ａ１ X is a hydrocarbon group having 6 to 40 carbon atoms. ａ１ Y is a hydrogen atom, a monovalent organic group, or a halogen atom. ａ１ is -O- or -NH-. The monomer is represented by (a2): CH2=C(-X ａ２ )-C(=O)-Y ａ２１ -Z(-Y ａ２２ -R ａ２ ) ｎ [In the formula, R ａ２ Each of these is independently a hydrocarbon group having 6 to 40 carbon atoms, X ａ２ Y is a hydrogen atom, a monovalent organic group, or a halogen atom. ａ２１ is -O- or -NH-, Y ａ２２ These are independent of each other, and can be directly bonded, or -O-, -C(=O)-, -S(=O) ２ -, -NH- or -CH ２ A monomer represented by ], where Z is a directly bonded or divalent or trivalent hydrocarbon group having 1 to 5 carbon atoms, and n is 1 or 2. 【0031】 ((a1) monomer) The monomer (a1) is given by the formula: CH2 = C(-X ａ１ )-C(=O)-Y ａ１ -R ａ１ [In the formula, R ａ１ X is a hydrocarbon group having 6 to 40 carbon atoms. ａ１ Y is a hydrogen atom, a monovalent organic group, or a halogen atom. ａ１It is a compound represented by -O- or -NH-. 【0032】 The monomer (a1) is Y ａ１ A long-chain acrylate ester monomer in which is -O-, or Y ａ１ It is a long-chain acrylamide monomer with -NH-. ａ１ This is preferably an aliphatic hydrocarbon group, particularly a saturated aliphatic hydrocarbon group, and especially an alkyl group. ａ１ In this, the number of carbon atoms in the hydrocarbon group is preferably 12 to 30, for example 16 to 26, and particularly preferably 18 to 22. ａ１ This may be a hydrogen atom, a methyl group, a halogen other than a fluorine atom, a substituted or unsubstituted benzyl group, or a substituted or unsubstituted phenyl group. A hydrogen atom, a methyl group, or a chlorine atom is preferred. 【0033】 Preferred examples of long-chain acrylate ester monomers are lauryl (meth)acrylate, stearyl (meth)acrylate, eicosyl (meth)acrylate, behenyl (meth)acrylate, stearyl α-chloroacrylate, eicosyl α-chloroacrylate, and behenyl α-chloroacrylate. Preferred examples of long-chain acrylamide monomers are stearyl (meth)acrylamide, eicosyl (meth)acrylamide, and behenyl (meth)acrylamide. 【0034】 ((a2) monomer) Monomer (a2) is a different monomer from monomer (a1). Monomer (a2) is -O-, -C(=O)-, -S(=O) ２ -, -NH- or -CH ２ It is a (meth)acrylate or (meth)acrylamide having a group composed of at least one selected from the following. The monomer (a2) is given by the formula: CH2=C(-X ａ２ )-C(=O)-Y ａ２１ -Z(-Y ａ２２ -R ａ２ ) ｎ [In the formula, R ａ２ Each of these is independently a hydrocarbon group having 6 to 40 carbon atoms, X ａ２ Y is a hydrogen atom, a monovalent organic group, or a halogen atom. ａ２１is -O- or -NH-, Y ａ２２ These are independent of each other, and can be directly bonded, or -O-, -C(=O)-, -S(=O) ２ -, -NH- or -CH ２ A compound represented by ] is a group composed of at least one selected from the following, where Z is a directly bonded, or divalent or trivalent hydrocarbon group having 1 to 5 carbon atoms, and n is 1 or 2. ａ２２ And / or Z does not have to be directly joined. Y ａ２２ And Z does not necessarily have to be in a direct bond at the same time. 【0035】 R ａ２ This is preferably an aliphatic hydrocarbon group, particularly a saturated aliphatic hydrocarbon group, and especially an alkyl group. ａ２ In this, the number of carbon atoms in the hydrocarbon group is preferably 12 to 30, for example 16 to 26 or 15 to 26, and particularly preferably 18 to 22 or 17 to 22. 【0036】 X ａ２ This may be a hydrogen atom, a methyl group, a halogen other than a fluorine atom, a substituted or unsubstituted benzyl group, or a substituted or unsubstituted phenyl group. A hydrogen atom, a methyl group, or a chlorine atom is preferred. 【0037】 Y ａ２２ -Y'-, -Y'-Y'-, -Y'-C(=O)-, -C(=O)-Y'-, -Y'-C(=O)-Y'-, -Y'-R'-, -Y'-R'-Y'-, -Y'-R'-Y'-C(=O)-, -Y'-R'-C(=O)-Y'-, -Y'-R'-Y'-C(=O)-Y'-, or -Y'-R'-Y'-R'- [where Y' is independent, directly combined, -O-, -NH-, or -S(=O)] ２ - and R' is - (CH ２ ) ｍ - (where m is an integer from 1 to 5), a linear hydrocarbon group having unsaturated bonds with 1 to 5 carbon atoms, a branched hydrocarbon group having 1 to 5 carbon atoms, or - (CH ２ ) ｌ -C ６ H ４ -(CH ２ ) ｌ- (where l is an independent integer from 0 to 5, and -C) ６ H ４ (- is a phenylene group). ] This may be the case. 【0038】 Y ａ２２ Specific examples include direct bond, -O-, -NH-, -OC(=O)-, -C(=O)-O-, -C(=O)-NH-, -NH-C(=O)-, -NH-S(=O) ２ -, -S (=O) ２ -NH-, -OC(=O)-NH-, -NH-C(=O)-O-, -NH-C(=O)-NH-, -OC ６ H ４ -, -NH-C ６ H ４ -, -O-(CH ２ ) m -O-, -NH-(CH ２ ) m -NH-, -O-(CH ２ ) m -NH-, -NH-(CH ２ ) m -O-, -O-(CH ２ ) m -O-C(=O)-, -O-(CH ２ ) m -C(=O)-O-, -NH-(CH ２ ) m -OC(=O)-, -NH-(CH ２ ) m -C(=O)-O-, -O-(CH ２ ) m -OC(=O)-NH-, -O-(CH ２ ) m -NH-C(=O)-O-, -O-(CH ２ ) m -C(=O)-NH-, -O-(CH ２ ) m -NH-C(=O)-, -O-(CH ２ ) m -NH-C(=O)-NH-, -O-(CH ２ ) m -O-C ６ H ４ -, -NH-(CH ２ ) m-OC(=O)-NH-, -NH-(CH ２ ) m -NH-C(=O)-O-, -NH-(CH ２ ) m -C(=O)-NH-, -NH-(CH ２ ) m -NH-C(=O)-, -NH-(CH ２ ) m -NH-C(=O)-NH-, -NH-(CH ２ ) m -O-C ６ H ４ -, -NH-(CH ２ ) m -NH-C ６ H ４ - [In the formula, m is an integer between 1 and 5.] 【0039】 Y ａ２２ is -O-, -NH-, -O-C(=O)-, -C(=O)-O-, -C(=O)-NH-, -NH-C(=O)-, -NH-S(=O) ２ -, -S (=O) ２ -NH-, -OC(=O)-NH-, -NH-C(=O)-O-, -NH-C(=O)-NH-, -OC ６ H ４ - is preferable. Y ａ２２ It is even more preferable that -NH-C(=O)-, -C(=O)-NH-, -O-C(=O)-NH-, -NH-C(=O)-O-, or -NH-C(=O)-NH-. ａ２２ The bond does not have to be direct. 【0040】 Z is a directly bonded, or divalent or trivalent hydrocarbon group having 1 to 5 carbon atoms, and may have a linear or branched structure. The number of carbon atoms in Z is preferably 2 to 4, particularly 2. Specific examples of Z include directly bonded, -CH ２ -ien-CH ２ CH ２ -ien-CH ２ CH ２ CH ２ -ien-CH ２ CH ２ CH ２ CH ２ -ien-CH２ CH ２ CH ２ CH ２ CH ２ -, having a branched structure - CH ２ CH=, has a branched structure -CH ２ (CH-)CH ２ -, having a branched structure - CH ２ CH ２ CH=, has a branched structure -CH ２ CH ２ CH ２ CH ２ CH=, has a branched structure -CH ２ CH ２ (CH-)CH ２ -, having a branched structure - CH ２ CH ２ CH ２ CH = . Z does not have to be a direct bond. 【0041】 The monomer (a2) is CH2=C(-X ａ２ )-C(=O)-O-(CH ２ ) m -NH-C(=O)-R ａ２ ,CH ２ = C(-X) ａ２ )-C(=O)-O-(CH ２ ) ｍ -OC(=O)-NH-R ａ２ ,CH ２ = C(-X) ａ２ )-C(=O)-O-(CH ２ ) ｍ -NH-C(=O)-OR ａ２ ,CH ２ = C(-X) ａ２ )-C(=O)-O-(CH ２ ) ｍ -NH-C(=O)-NH-R ａ２ It is preferable that R ａ２ and X ａ２ This is equivalent to the above. ]. The monomer (a2) is CH2=C(-X ａ２ )-C(=O)-O-(CH ２ ) m -NH-C(=O)-R ａ２ It is particularly preferable that this be the case. 【0042】 Monomer (a2) can be produced by reacting a hydroxyalkyl (meth)acrylate or hydroxyalkyl (meth)acrylamide with a long-chain alkyl isocyanate. Examples of long-chain alkyl isocyanates include lauryl isocyanate, myristyl isocyanate, cetyl isocyanate, stearyl isocyanate, oleyl isocyanate, and behenyl isocyanate. Alternatively, monomer (a2) can also be produced by reacting a (meth)acrylate having an isocyanate group in its side chain, such as 2-methacryloyloxyethyl methacrylate, with a long-chain alkylamine or long-chain alkyl alcohol. Examples of long-chain alkylamines include laurylamine, myristylamine, cetylamine, stearylamine, oleylamine, and behenylamine. Examples of long-chain alkyl alcohols include lauryl alcohol, myristyl alcohol, cetyl alcohol, stearyl alcohol, oleyl alcohol, and behenyl alcohol. 【0043】 Preferred examples of monomer (a) are as follows: stearyl (meth)acrylate, behenyl (meth)acrylate, stearyl α-chloroacrylate, behenyl α-chloroacrylate; stearyl (meth)acrylamide, behenyl (meth)acrylamide; 【0044】 【0045】 【0046】 【0047】 【0048】 【0049】 [In the above formula, n is a number from 6 to 40, and m is a number from 1 to 5.] The compound in the above chemical formula is an acrylic compound in which the α-position is a hydrogen atom, but specific examples may be a methacle compound in which the α-position is a methyl group and an α-chloroacrylic compound in which the α-position is a chlorine atom. 【0050】 The monomer (a2) is given by formula: R ａ２２ -C(=O)-NH-R ａ２３ -O-R ａ２１ [In the formula, R ａ２１ R is an organic residue having an ethylenically unsaturated polymerizable group. ａ２２ R is a hydrocarbon group having 6 to 40 carbon atoms. ａ２３ It is preferably an amide group-containing monomer represented by ], which is a hydrocarbon group having 1 to 5 carbon atoms. 【0051】 R ａ２１ This is an organic residue having an ethylenically unsaturated polymerizable group, and is not particularly limited as long as it has a double bond between carbon atoms. Specifically, -C(=O)CR ａ２１１ =CH ２ ----CHR ａ２１１ =CH ２ ien-CH ２ CHR ａ２１１ =CH ２ Examples include organic residues having ethylenically unsaturated polymerizable groups, such as R ａ２１１ Examples include a hydrogen atom or an alkyl group having 1 to 4 carbon atoms. Also, R ａ２１ In addition to ethylenically unsaturated polymerizable groups, it may have various organic groups, such as chain hydrocarbons, cyclic hydrocarbons, polyoxyalkylene groups, and polysiloxane groups, and these organic groups may be substituted with various substituents. ａ２１ -C(=O)CR ａ２１１ =CH ２ It is preferable that this be the case. 【0052】 R ａ２２ This is a hydrocarbon group having 6 to 40 carbon atoms, preferably an alkyl group, and includes chain hydrocarbon groups, cyclic hydrocarbon groups, etc. Among these, a chain hydrocarbon group is preferred, and a linear saturated hydrocarbon group is particularly preferred. ａ２２ The number of carbon atoms is 6 to 40, preferably 11 to 27, and particularly preferably 15 to 23. 【0053】 R ａ２３This is a hydrocarbon group having 1 to 5 carbon atoms, preferably an alkyl group. The hydrocarbon group having 1 to 5 carbon atoms may be linear or branched, and may have unsaturated bonds, but linear is preferred. ａ２３ The number of carbon atoms is preferably 2 to 4, and particularly preferably 2. ａ２３ It is preferable that it is an alkylene group. 【0054】 A monomer containing an amide group is R ａ２２ Those that have only one type (for example, R ａ２２ (only compounds with 17 carbon atoms), or R ａ２２ Those that are combinations of multiple things (for example, R ａ２２ A compound with 17 carbon atoms and R ａ２２ It may be a mixture of a compound having 15 carbon atoms. 【0055】 An example of an amide group-containing monomer is alkyl (meth)acrylate carboxylic acid amide. Specific examples of amide group-containing monomers include palmitic acid amide ethyl (meth)acrylate, stearic acid amide ethyl (meth)acrylate, behenic acid amide ethyl (meth)acrylate, myristate acid amide ethyl (meth)acrylate, lauric acid amide ethyl (meth)acrylate, isostearate ethyl amide (meth)acrylate, oleic acid ethyl amide (meth)acrylate, tert-butylcyclohexylcaproic acid amide ethyl (meth)acrylate, adamantane carboxylic acid ethyl amide (meth)acrylate, naphthalene carboxylic acid amide ethyl (meth)acrylate, anthracene carboxylic acid amide ethyl (meth)acrylate, palmitic acid amide propyl (meth)acrylate, stearate amide propyl (meth)acrylate, palmitic acid amide ethyl vinyl ether, stearate amide ethyl vinyl ether, palmitic acid amide ethyl allyl ether, stearate amide ethyl allyl ether, or mixtures thereof. 【0056】The amide group-containing monomer is preferably stearamide ethyl (meth)acrylate. The amide group-containing monomer may be a mixture containing stearamide ethyl (meth)acrylate. In a mixture containing stearamide ethyl (meth)acrylate, the amount of stearamide ethyl (meth)acrylate may be, for example, 40% or more by weight, 50% or more by weight, 60% or more by weight, or 70% or more by weight, or 90% or less by weight, 80% or less by weight, or 70% or less by weight, based on the total weight of the amide group-containing monomer. The remaining monomer may be, for example, palmitic acid amide ethyl (meth)acrylate. 【0057】 Of monomer (a), the amount of monomer (a2) may be 10% by weight or more, 20% by weight or more, 30% by weight or more, 40% by weight or more, 50% by weight or more, 60% by weight or more, 70% by weight or more, or 80% by weight or more, and is preferably 30% by weight or more. 【0058】 [(b) Hydrophilic group-containing monomer] The hydrocarbon-containing polymer (1) may contain repeating units derived from the hydrophilic group-containing monomer (b). Monomer (b) is a monomer other than monomer (a) that has a hydrophilic group. The hydrophilic group is preferably an oxyalkylene group (the alkylene group has 2 to 6 carbon atoms), and more preferably an oxyethylene group. In particular, monomer (b) is preferably an oxyalkylene (meth)acrylate, for example, polyalkylene (or monoalkylene) glycol mono(meth)acrylate and / or polyalkylene (or monoalkylene) glycol di(meth)acrylate, or polyalkylene (or monoalkylene) glycol mono(meth)acrylamide. 【0059】 Monomer (b) is given by formula: CH ２ = CX ｂ C(=O)-Y ｂ - (R ｂ O) ｎ -A ｂ [In the formula, X ｂ is a hydrogen atom or a methyl group, Y ｂ is -O- or -NH-, and R ｂEach of these is an alkylene group having 2 to 6 carbon atoms, and A ｂ This is a hydrogen atom, an unsaturated or saturated hydrocarbon group having 1 to 22 carbon atoms, or CH ２ = CX ｂ It is preferable that the oxyalkylene (meth)acrylate is represented by [C(=O)-, where n is an integer from 1 to 90]. 【0060】 An example of monomer (b) is given by formula: CH ２ = CX ｂ C(=O)-O-(R ｂ O) ｎ -A ｂｉ (b1) CH ２ = CX ｂ C(=O)-O-(R ｂ O) ｎ -C(=O)CX ｂ =CH ２ (b2), or CH ２ = CX ｂ C(=O)-NH-(R ｂ O) ｎ -A ｂｉ (b3) [In the formula, X ｂ Each is independently a hydrogen atom or a methyl group, R ｂ Each of these is an alkylene group having 2 to 6 carbon atoms, and A ｂｉ Each is independently a hydrogen atom or an unsaturated or saturated hydrocarbon group having 1 to 22 carbon atoms, and n is an integer from 1 to 90. Preferably, these are represented by [ ] (each being monomer (b1), monomer (b2), or monomer (b3)). 【0061】 n may be, for example, 1 to 50, especially 1 to 30, particularly 1 to 15, or 2 to 15. Alternatively, n may be, for example, 1. ｂ This may be a linear or branched alkylene group, for example, formula -(CH ２ ) ｘ - or - (CH ２ ) ｘ１ - (CH(CH ３ )) ｘ２-[In the formula, x1 and x2 are between 0 and 6, for example, 2 and 5, and the sum of x1 and x2 is between 1 and 6. -(CH ２ ) ｘ１ - and - (CH (CH ３ )) ｘ２ The order of the hyphens is not limited to the given formula and may be random. The base may be represented by ]. - (R ｂ O) n -In this case, R may be of two or more types (for example, 2 to 4 types, especially 2 types), -(R ｂ O) n - is, for example, - (R １ O) ｎ１ - and - (R ２ O) ｎ２ - [wherein, R １ and R ２ The combination may be: 1, n1 and n2 are mutually distinct alkylene groups having 2 to 6 carbon atoms, n1 and n2 are numbers of 1 or more, and the sum of n1 and n2 is 2 to 90. 【0062】 R in equations (b1), (b2), and (b3) ｂ R is particularly preferably an ethylene group, a propylene group, or a butylene group, and especially preferably a butylene group. ｂ R may be a combination of two or more alkylene groups. In that case, it is preferable that at least one of R is an ethylene group, a propylene group, or a butylene group. ｂ Examples of combinations include ethylene group / propylene group combinations, ethylene group / butylene group combinations, and propylene group / butylene group combinations. Monomer (b) may be a mixture of two or more types. In that case, at least one of monomer (b) is R in formula (b1), (b2), or (b3). ｂ It is preferable that the group is an ethylene group, a propylene group, or a butylene group. Furthermore, when using polyalkylene glycol di(meth)acrylate represented by formula (b2), it is not preferable to use it alone as monomer (b), but rather to use it in combination with monomer (b1). In that case as well, it is preferable that the compound represented by formula (b2) be kept to less than 30% by weight of monomer (b) used. 【0063】Specific examples of the monomer (b) can be exemplified by, for example, the following, but are not limited thereto. CH2=CHCOO-CH2CH2O-H CH2=CHCOO-CH2CH2CH2O-H CH2=CHCOO-CH2CH(CH3)O-H CH2=CHCOO-CH(CH3)CH2O-H CH2=CHCOO-CH2CH2CH2CH2O-H CH2=CHCOO-CH2CH2CH(CH3)O-H CH2=CHCOO-CH2CH(CH3)CH2O-H CH2=CHCOO-CH(CH3)CH2CH2O-H CH2=CHCOO-CH2CH(CH2CH3)O-H CH2=CHCOO-CH2C(CH3)2O-H CH2=CHCOO-CH(CH2CH3)CH2O-H CH2=CHCOO-C(CH3)2CH2O-H CH2=CHCOO-CH(CH3)CH(CH3)O-H CH2=CHCOO-C(CH3)(CH2CH3)O-H CH2=CHCOO-(CH2CH2O)2-H CH2=CHCOO-(CH2CH2O)4-H CH2=CHCOO-(CH2CH2O)5-H CH2=CHCOO-(CH2CH2O)6-H CH2=CHCOO-(CH2CH2O)5-CH3 CH2=CHCOO-(CH2CH2O)9-CH3 CH2=CHCOO-(CH2CH2O) 23 -CH3 CH2=CHCOO-(CH2CH2O) 90 -CH3 【0064】 CH2=CHCOO-(CH2CH(CH3)O)9-H CH2=CHCOO-(CH2CH(CH3)O)9-CH3 CH2=CHCOO-(CH2CH(CH3)O) 12 -CH3 CH2=CHCOO-(CH2CH2O)5-(CH2CH(CH3)O)2-H CH2=CHCOO-(CH2CH2O)5-(CH2CH(CH3)O)3-CH3 CH2=CHCOO-(CH2CH2O)8-(CH2CH(CH3)O)6-CH2CH(C2H5)C4H9 CH2=CHCOO-(CH2CH2O) 23 -OOC(CH3)C=CH2 CH2=CHCOO-(CH2CH2O) 20 -(CH2CH(CH3)O)5-CH2-CH=CH2 【0065】CH2=CHCOO-(CH2CH2O)9-H CH2=C(CH3)COO-CH2CH2O-H CH2=C(CH3)COO-CH2CH2CH2O-H CH2=C(CH3)COO-CH2CH(CH3)O-H CH2=C(CH3)COO-CH(CH3)CH2O-H CH2=C(CH3)COO-CH2CH2CH2CH2O-H CH2=C(CH3)COO-CH2CH2CH(CH3)O-H CH2=C(CH3)COO-CH2CH(CH3)CH2O-H CH2=C(CH3)COO-CH(CH3)CH2CH2O-H CH2=C(CH3)COO-CH2CH(CH2CH3)O-H CH2=C(CH3)COO-CH2C(CH3)2O-H CH2=C(CH3)COO-CH(CH2CH3)CH2O-H CH2=C(CH3)COO-C(CH3)2CH2O-H CH2=C(CH3)COO-CH(CH3)CH(CH3)O-H CH2=C(CH3)COO-C(CH3)(CH2CH3)O-H CH2=C(CH3)COO-(CH2CH2O)2-H CH2=C(CH3)COO-(CH2CH2O)4-H CH2=C(CH3)COO-(CH2CH2O)5-H CH2=C(CH3)COO-(CH2CH2O)6-H CH2=C(CH3)COO-(CH2CH2O)9-H CH2=C(CH3)COO-(CH2CH2O)5-CH3 CH2=C(CH3)COO-(CH2CH2O)9-CH3 CH2=C(CH3)COO-(CH2CH2O) 23 -CH3 CH2=C(CH3)COO-(CH2CH2O) 90 -CH3 CH2=C(CH3)COO-(CH2CH(CH3)O)9-H 【0066】 CH2=C(CH3)COO-(CH2CH(CH3)O)9-CH3 CH2=C(CH3)COO-(CH2CH(CH3)O) 12-CH3 CH2=C(CH3)COO-(CH2CH2O)5-(CH2CH(CH3)O)2-H CH2=C(CH3)COO-(CH2CH2O)5-(CH2CH(CH3)O)3-CH3 CH2=C(CH3)COO-(CH2CH2O)8-(CH2CH(CH3)O)6-CH2CH(C2H5)C4H9 CH2=C(CH3)COO-(CH2CH2O) 23 -OOC(CH3)C=CH2 CH2=C(CH3)COO-(CH2CH2O) 20 -(CH2CH(CH3)O)5-CH2-CH=CH2 【0067】 CH2=CH-C(=O)-NH-CH2CH2O-H CH2=CH-C(=O)-NH-CH2CH2CH2O-H CH2=CH-C(=O)-NH-CH2CH(CH3)OH CH2=CH-C(=O)-NH-CH(CH3)CH2O-H CH2=CH-C(=O)-NH-CH2CH2CH2CH2O-H CH2=CH-C(=O)-NH-CH2CH2CH(CH3)OH CH2=CH-C(=O)-NH-CH2CH(CH3)CH2O-H CH2=CH-C(=O)-NH-CH(CH3)CH2CH2O-H CH2=CH-C(=O)-NH-CH2CH(CH2CH3)OH CH2=CH-C(=O)-NH-CH2C(CH3)2O-H CH2=CH-C(=O)-NH-CH(CH2CH3)CH2O-H CH2=CH-C(=O)-NH-C(CH3)2CH2O-H CH2=CH-C(=O)-NH-CH(CH3)CH(CH3)OH CH2=CH-C(=O)-NH-C(CH3)(CH2CH3)OH CH2=CH-C(=O)-NH-(CH2CH2O)2-H CH2=CH-C(=O)-NH-(CH2CH2O)4-H CH2=CH-C(=O)-NH-(CH2CH2O)5-H CH2=CH-C(=O)-NH-(CH2CH2O)6-H CH2=CH-C(=O)-NH-(CH2CH2O)9-H CH2=CH-C(=O)-NH-(CH2CH2O)5-CH3 CH2=CH-C(=O)-NH-(CH2CH2O)9-CH3 CH2=CH-C(=O)-NH-(CH2CH2O) 23-CH3 CH2=CH-C(=O)-NH-(CH2CH2O) 90 -CH3 【0068】 CH2=CH-C(=O)-NH-(CH2CH(CH3)O)9-H CH2=CH-C(=O)-NH-(CH2CH(CH3)O)9-CH3 CH2=CH-C(=O)-NH-(CH2CH(CH3)O) 12 -CH3 CH2=CH-C(=O)-NH-(CH2CH2O)5-(CH2CH(CH3)O)2-H CH2=CH-C(=O)-NH-(CH2CH2O)5-(CH2CH(CH3)O)3-CH3 CH2=CH-C(=O)-NH-(CH2CH2O)8-(CH2CH(CH3)O)6-CH2CH(C2H5)C4H9 【0069】CH2=C(CH3)-C(=O)-NH-CH2CH2O-H CH2=C(CH3)-C(=O)-NH-CH2CH2CH2O-H CH2=C(CH3)-C(=O)-NH-CH2CH(CH3)OH CH2=C(CH3)-C(=O)-NH-CH(CH3)CH2O-H CH2=C(CH3)-C(=O)-NH-CH2CH2CH2CH2O-H CH2=C(CH3)-C(=O)-NH-CH2CH2CH(CH3)OH CH2=C(CH3)-C(=O)-NH-CH2CH(CH3)CH2O-H CH2=C(CH3)-C(=O)-NH-CH2CH(CH3)CH2O-H CH2=C(CH3)-C(=O)-NH-CH2CH(CH3)CH2O-H CH2=C(CH3)-C(=O)-NH-CH2CH(CH2CH3)OH CH2=C(CH3)-C(=O)-NH-CH2C(CH3)2O-H CH2=C(CH3)-C(=O)-NH-CH(CH2CH3)CH2O-H CH2=C(CH3)-C(=O)-NH-C(CH3)2CH2O-H CH2=C(CH3)-C(=O)-NH-CH(CH3)CH(CH3)OH CH2=C(CH3)-C(=O)-NH-C(CH3)(CH2CH3)OH CH2=C(CH3)-C(=O)-NH-C(CH3)(CH2CH3)OH CH2=C(CH3)-C(=O)-NH-(CH2CH2O)2-H CH2=C(CH3)-C(=O)-NH-(CH2CH2O)4-H CH2=C(CH3)-C(=O)-NH-(CH2CH2O)5-H CH2=C(CH3)-C(=O)-NH-(CH2CH2O)6-H CH2=C(CH3)-C(=O)-NH-(CH2CH2O)9-H CH2=C(CH3)-C(=O)-NH-(CH2CH2O)5-CH3 CH2=C(CH3)-C(=O)-NH-(CH2CH2O)9-CH3 CH2=C(CH3)-C(=O)-NH-(CH2CH2O) 23 -CH3 CH2=C(CH3)-C(=O)-NH-(CH2CH2O) 90 -CH3 【0070】 CH2=C(CH3)-C(=O)-NH-(CH2CH(CH3)O)9-H CH2=C(CH3)-C(=O)-NH-(CH2CH(CH3)O)9-CH3 CH2=C(CH3)-C(=O)-NH-(CH2CH(CH3)O) 12-CH3 CH2=C(CH3)-C(=O)-NH-(CH2CH2O)5-(CH2CH(CH3)O)2-H CH2=C(CH3)-C(=O)-NH-(CH2CH2O)5-(CH2CH(CH3)O)3-CH3 CH2=C(CH3)-C(=O)-NH-(CH2CH2O)8-(CH2CH(CH3)O)6-CH2CH(C2H5)C4H9 【0071】 The monomer (b) is X ２ It is preferable that the monomer (b) is a hydrogen atom and is an acrylate or acrylamide. Monomer (b) is particularly preferably hydroxyethyl acrylate, hydroxypropyl acrylate, hydroxybutyl acrylate, or hydroxyethyl acrylamide. 【0072】 [(c) Ionic group-containing monomer] The hydrocarbon-containing polymer (1) may contain repeating units derived from the ionic group-containing monomer (c). Monomer (c) is a monomer other than monomer (a) and monomer (b). Monomer (c) is preferably a monomer containing an olefinic carbon-carbon double bond and an ionic group (particularly an acrylic monomer). The ionic group is an anionic group and / or a cationic group. 【0073】 Monomers having anionic groups include monomers having a carboxyl group, a sulfonic acid group, or a phosphate group. Specific examples of monomers having anionic groups include (meth)acrylic acid, crotonic acid, maleic acid, fumaric acid, itaconic acid, citraconic acid, vinylsulfonic acid, (meth)allylsulfonic acid, styrenesulfonic acid, (meth)acrylate phosphoric acid, vinylbenzenesulfonic acid, acrylamide tert-butylsulfonic acid, or salts thereof. 【0074】 Examples of salts of anionic groups include alkali metal salts, alkaline earth metal salts, or ammonium salts, such as methylammonium salt, ethanolammonium salt, and triethanolammonium salt. 【0075】In monomers having cationic groups, examples of cationic groups are amino groups, preferably tertiary amino groups and quaternary amino groups. In tertiary amino groups, the two groups bonded to the nitrogen atom are the same or different, and are an aliphatic group having 1 to 5 carbon atoms (especially alkyl groups), an aromatic group having 6 to 20 carbon atoms (aryl groups), or an aromatic aliphatic group having 7 to 25 carbon atoms (especially aralkyl groups, such as benzyl groups (C)). ６ H ５ -CH ２ It is preferable that the quaternary amino group is a C1-C5 aliphatic group (especially alkyl group), a C6-C20 aromatic group (aryl group), or a C7-C25 aromatic aliphatic group (especially aralkyl group, for example benzyl group (C)). ６ H ５ -CH ２ It is preferable that the tertiary amino group and quaternary amino group have a carbon-carbon double bond remaining to the nitrogen atom. The cationic group may be in the form of a salt. 【0076】 The cationic group, which is a salt, is a salt with an acid (organic or inorganic acid). Organic acids, such as carboxylic acids having 1 to 20 carbon atoms (especially monocarboxylic acids such as acetic acid, propionic acid, butyric acid, and stearic acid), are preferred. Dimethylaminoethyl (meth)acrylate and diethylaminoethyl (meth)acrylate and their salts are preferred. 【0077】Specific examples of monomers having cationic groups are as follows: CH2=CHCOO-CH2CH2-N(CH3)2 and its salts (e.g., acetate) CH2=CHCOO-CH2CH2-N(CH2CH3)2 and its salts (e.g., acetate) CH2=C(CH3)COO-CH2CH2-N(CH3)2 and its salts (e.g., acetate) CH2=C(CH3)COO-CH2CH2-N(CH2CH3)2 and its salts (e.g., acetate) CH2=CHC(O)N(H)-CH2CH2CH2-N(CH3)2 and its salts (e.g., acetate) CH2=CHCOO-CH2CH2-N(-CH3)(-CH2-C6H5) and its salts (e.g., acetate) CH2=C(CH3)COO-CH2CH2-N(-CH2CH3)(-CH2-C6H5) and its salts (e.g., acetate) CH2=CHCOO-CH2CH2-N + (CH3)3Cl - CH2=CHCOO-CH2CH2-N + (-CH3)2(-CH2-C6H5)Cl - CH2=C(CH3)COO-CH2CH2-N + (CH3)3Cl - CH2=CHCOO-CH2CH(OH)CH2-N + (CH3)3Cl - CH2=C(CH3)COO-CH2CH(OH)CH2-N + (CH3)3Cl - CH2=C(CH3)COO-CH2CH(OH)CH2-N + (-CH2CH3)2(-CH2-C6H5)Cl - CH2=C(CH3)COO-CH2CH2-N + (CH3)3Br - CH2=C(CH3)COO-CH2CH2-N + (CH3)3I - CH2=C(CH3)COO-CH2CH2-N + (CH3)3O - SO3CH3 CH2=C(CH3)COO-CH2CH2-N + (CH3)(-CH2-C6H5)2Br - 【0078】The ionic group-containing monomer (c) is preferably methacrylic acid, acrylic acid, or dimethylaminoethyl methacrylate, and more preferably methacrylic acid or dimethylaminoethyl methacrylate. 【0079】 [(d) Other monomers] The hydrocarbon-containing polymer (1) may have repeating units derived from monomers other than monomers (a) to (c). Examples of other monomers include halogenated olefin monomers and crosslinkable monomers. 【0080】 (Halogenated Olefin Monomer) The hydrocarbon-containing polymer (1) may have repeating units derived from halogenated olefin monomers. Preferably, the halogenated olefin monomer does not have fluorine atoms. Preferably, the halogenated olefin monomer is an olefin having 2 to 20 carbon atoms substituted with 1 to 10 chlorine atoms, bromine atoms, or iodine atoms. Preferably, the halogenated olefin monomer is a chlorinated olefin having 2 to 20 carbon atoms, and more preferably, an olefin having 2 to 5 carbon atoms having 1 to 5 chlorine atoms. Preferred specific examples of halogenated olefin monomers are halogenated vinyl, for example, vinyl chloride, vinyl bromide, vinyl iodide, and halogenated vinylide, for example, vinylidene chloride, vinylidene bromide, and vinylidene iodide. Vinyl chloride is preferred because it has high water repellency (especially water repellency durability). The presence of repeating units derived from halogenated olefin monomers increases the wash durability provided by the hydrocarbon-containing polymer (1). 【0081】(Crossable Monomer) The hydrocarbon-containing polymer (1) has a crosslinkable monomer having at least two reactive groups and / or ethylenically unsaturated double bonds (preferably (meth)acrylate groups), and the crosslinkable monomer (d) may be a monomer that does not contain fluorine atoms. It may be a compound that does not contain fluorine atoms. The crosslinkable monomer (d) may be a compound having at least two ethylenically unsaturated double bonds (preferably (meth)acrylate groups), or a compound having at least one ethylenically unsaturated double bond and at least one reactive group. Examples of reactive groups are hydroxyl groups, epoxy groups, chloromethyl groups, blocked isocyanate groups, amino groups, carboxyl groups, etc. 【0082】 The crosslinkable monomer may be a mono(meth)acrylate, di(meth)acrylate, or mono(meth)acrylamide having a reactive group. Alternatively, the crosslinkable monomer may be a di(meth)acrylate. 【0083】 One example of a crosslinkable monomer is a vinyl monomer having a hydroxyl group. Examples of crosslinkable monomers include, but are not limited to, diacetone (meth)acrylamide, 3-chloro-2-hydroxypropyl (meth)acrylate, 2-acetoacetoxyethyl (meth)acrylate, butadiene, isoprene, chloroprene, vinyl monochloroacetate, vinyl methacrylate, glycidyl (meth)acrylate, 1,4-butanediol di(meth)acrylate, 1,6-hexanediol di(meth)acrylate, 1,9-nonanediol di(meth)acrylate, and neopentyl glycol di(meth)acrylate. 【0084】 (Cyclic hydrocarbon group-containing monomer) The hydrocarbon-containing polymer (1) may have a cyclic hydrocarbon group-containing monomer. The cyclic hydrocarbon group-containing monomer is a monomer having a cyclic hydrocarbon group, and may be a monomer having one ethylenically unsaturated double bond and a cyclic hydrocarbon group. 【0085】The monomer containing the cyclic hydrocarbon group preferably has a (meth)acrylic group as the ethylenically unsaturated double bond, for example, it may have a (meth)acrylate group or a (meth)acrylamide group as the ethylenically unsaturated double bond. 【0086】 The cyclic hydrocarbon group may be alicyclic or aromatic, and is preferably alicyclic. The cyclic hydrocarbon group may be saturated or unsaturated, and is preferably saturated. The cyclic hydrocarbon group may be monocyclic, polycyclic, or crosslinked, and is preferably crosslinked. The cyclic hydrocarbon group may have a chain-like group (for example, a linear or branched hydrocarbon group). 【0087】 The number of carbon atoms in the cyclic hydrocarbon group may be 4 or more, 6 or more, or 8 or more, and may be 30 or less, 26 or less, 22 or less, 18 or less, or 14 or less. 【0088】 Specific examples of cyclic hydrocarbon groups include cyclohexyl group, t-butylcyclohexyl group, adamantyl group, 2-methyl-2-adamantyl group, 2-ethyl-2-adamantyl group, bornyl group, isobornyl group, norbornyl group, dicyclopentanyl group, dicyclopentenyl group, benzyl group, phenyl group, naphthyl group, 2-t-butylphenyl group, residues obtained by removing one or more hydrogen atoms from these groups (e.g., cyclohexylene group, adamantylene group, phenylene group, naphthylene group, etc.), and substituted groups thereof. 【0089】Specific examples of monomers containing cyclic hydrocarbon groups include cyclohexyl (meth)acrylate, t-butylcyclohexyl (meth)acrylate, benzyl (meth)acrylate, isobornyl (meth)acrylate, dicyclopentanyl (meth)acrylate, dicyclopentenyl (meth)acrylate, dicyclopentanyloxyethyl (meth)acrylate, tricyclopentanyl (meth)acrylate, adamantyl (meth)acrylate, 2-methyl-2-adamantyl (meth)acrylate, 2-ethyl-2-adamantyl (meth)acrylate, compounds in which these acrylates are substituted with acrylamide, styrene, α-methylstyrene, p-methylstyrene, etc. These may be used alone or in combination of two or more. 【0090】 Other monomers (d) are not limited to these examples and include acrylonitrile, organosiloxane-containing (meth)acrylates, short-chain alkyl (meth)acrylates, vinyl acetate, vinyl alkyl ethers, etc. Other monomers (d) may be used alone or in combination of two or more. 【0091】 [Composition of Polymer (1)] The combinations of monomers that constitute the repeating units of the hydrocarbon-containing polymer (1) are, for example, as follows: Monomer (a) Monomer (a) + monomer (b) Monomer (a) + monomer (c) Monomer (a) + monomer (b) + monomer (c) Monomer (a) + monomer (b) + monomer (d) Monomer (a) + monomer (c) + monomer (d) Monomer (a) + monomer (b) + monomer (c) + monomer (d) Preferably, the combination of monomers that constitute the repeating units of the polymer is "monomer (a) + monomer (b) + monomer (c)". 【0092】The amount of repeating units (repeating unit (a)) formed from monomer (a) may be 30% by weight or more, 40% by weight or more, 50% by weight or more, 60% by weight or more, 70% by weight or more, 80% by weight or more, or 90% by weight or more, relative to the hydrocarbon-containing polymer (1) (or relative to the total of repeating unit (a) and repeating unit (b)), for example, 75% by weight or more, and may also be 95% by weight or less, 85% by weight or less, 75% by weight or less, 65% by weight or less, 55% by weight or less, or 45% by weight or less. 【0093】 The amount of repeating units (repeating unit (b)) formed from monomer (b) may be 3% by weight or more, 5% by weight or more, 10% by weight or more, 15% by weight or more, 20% by weight or more, or 25% by weight or more with respect to the hydrocarbon-containing polymer (1) (or the total of repeating unit (a) and repeating unit (b)), for example, 5% by weight or more, and may also be 50% by weight or less, 40% by weight or less, 30% by weight or less, 20% by weight or less, 10% by weight or less, or 5% by weight or less. 【0094】 The amount of repeating units (repeating unit (c)) formed from monomer (c) may be 2% by weight or more, 5% by weight or more, 10% by weight or more, 15% by weight or more, 20% by weight or more, or 25% by weight or more, relative to the hydrocarbon-containing polymer (1) (or relative to the total of repeating units (a) and repeating units (b)), and may also be 50% by weight or less, 40% by weight or less, 30% by weight or less, 20% by weight or less, 10% by weight or less, or 5% by weight or less. 【0095】 The amount of repeating units (repeating unit (d)) formed from monomer (d) may be 1% by weight or more, 5% by weight or more, 10% by weight or more, 15% by weight or more, 20% by weight or more, or 25% by weight or more, relative to the hydrocarbon-containing polymer (1) (or relative to the sum of repeating units (a) and repeating units (b)), and may also be 50% by weight or less, 40% by weight or less, 30% by weight or less, 20% by weight or less, 10% by weight or less, or 5% by weight or less. 【0096】[Polymerization Method] The hydrocarbon-containing polymer (1) can be produced by known polymerization methods, and the conditions for the polymerization reaction can be arbitrarily selected. Examples of such polymerization methods include solution polymerization, suspension polymerization, emulsion polymerization, and condensation polymerization. 【0097】 In solution polymerization, a method is employed in which monomers are dissolved in an organic solvent in the presence of a polymerization initiator, followed by nitrogen purging, and then heating and stirring at a temperature of 30 to 120°C for 1 to 10 hours. Examples of polymerization initiators include azobisisobutyronitrile, benzoyl peroxide, di-t-butyl peroxide, lauryl peroxide, cumene hydroperoxide, t-butyl peroxypivalate, and diisopropyl peroxydicarbonate. The polymerization initiator is used in an amount of 0.01 to 20 parts by weight, for example, 0.01 to 10 parts by weight, per 100 parts by weight of monomer. 【0098】 Organic solvents are inert to monomers and dissolve them, and may include esters (e.g., esters with 2 to 40 carbon atoms, specifically ethyl acetate and butyl acetate), ketones (e.g., ketones with 2 to 40 carbon atoms, specifically methyl ethyl ketone, diisobutyl ketone, and methyl isobutyl ketone), and alcohols (e.g., alcohols with 1 to 40 carbon atoms, specifically ethanol, butanol, and isopropyl alcohol). Specific examples of organic solvents include acetone, chloroform, HCHC225, isopropyl alcohol, cyclohexane, benzene, toluene, xylene, petroleum ether, tetrahydrofuran, 1,4-dioxane, methyl ethyl ketone, methyl isobutyl ketone, diisobutyl ketone, ethyl acetate, butyl acetate, 1,1,2,2-tetrachloroethane, 1,1,1-trichloroethane, trichloroethylene, perchloroethylene, tetrachlorodifluoroethane, and trichlorotrifluoroethane. The organic solvent is used in an amount of 10 to 3000 parts by weight, for example, 50 to 2000 parts by weight, per 100 parts by weight of the total monomers. 【0099】Water-soluble organic solvents may be used as organic solvents. For example, water-soluble organic solvents such as ketones (e.g., acetone, methyl ethyl ketone, etc.) or alcohols (e.g., propylene glycol, dipropylene glycol monomethyl ether, dipropylene glycol, tripropylene glycol, ethanol, etc.) may be used. 【0100】 In emulsion polymerization, a method is employed in which monomers are emulsified in water in the presence of a polymerization initiator and an emulsifier, and then polymerized by stirring at a temperature of 50 to 80°C for 1 to 20 hours after nitrogen purging. The polymerization initiators used are water-soluble ones such as benzoyl peroxide, lauroyl peroxide, t-butyl perbenzoate, 1-hydroxycyclohexyl hydroperoxide, 3-carboxypropionyl peroxide, acetyl peroxide, azobisisobutylamidine dihydrochloride, sodium peroxide, potassium persulfate, and ammonium persulfate, or oil-soluble ones such as azobisisobutyronitrile, benzoyl peroxide, di-t-butyl peroxide, lauryl peroxide, cumene hydroperoxide, t-butyl peroxypivalate, and diisopropyl peroxydicarbonate. The polymerization initiator is used in an amount of 0.01 to 20 parts by weight, for example, 0.01 to 10 parts by weight, per 100 parts by weight of monomer. 【0101】 To obtain a polymer aqueous dispersion with excellent stability during storage, it is desirable to polymerize the monomers by micronizing them in water using an emulsifying device that can impart strong crushing energy, such as a high-pressure homogenizer or an ultrasonic homogenizer. Various emulsifiers, including anionic, cationic, and nonionic types, can be used as emulsifiers, and are used in an amount ranging from 0.5 to 20 parts by weight per 100 parts by weight of monomer. It is preferable to use anionic and / or nonionic and / or cationic emulsifiers. If the monomers are not completely miscible, it is preferable to add a compatibilizer that allows them to be sufficiently miscible, such as a water-soluble organic solvent or a low molecular weight monomer. Adding a compatibilizer can improve emulsification and copolymerization properties. 【0102】As the water-soluble organic solvent, the organic solvents mentioned above may be used. For example, acetone, methyl ethyl ketone, ethyl acetate, propylene glycol, dipropylene glycol monomethyl ether, dipropylene glycol, tripropylene glycol, ethanol, etc., may be used in a range of 1 to 50 parts by weight, for example, 10 to 40 parts by weight, per 100 parts by weight of water. In addition, as low molecular weight monomers, methyl methacrylate, glycidyl methacrylate, 2,2,2-trifluoroethyl methacrylate, etc., may be used in a range of 1 to 50 parts by weight, for example, 10 to 40 parts by weight, per 100 parts by weight of the total amount of monomers. 【0103】 In polymerization, a chain transfer agent may be used. The molecular weight of the polymer can be changed depending on the amount of chain transfer agent used. Examples of chain transfer agents include mercaptan group-containing compounds such as lauryl mercaptan, thioglycol, and thioglycerol (especially alkyl mercaptans (e.g., with 1 to 40 carbon atoms)), and inorganic salts such as sodium hypophosphite and sodium bisulfite. The amount of chain transfer agent used may be in the range of 0.01 to 10 parts by weight, for example, 0.1 to 5 parts by weight, per 100 parts by weight of the total amount of monomer. 【0104】 [Amount of hydrocarbon group-containing polymer (1)] The amount of hydrocarbon group-containing polymer (1) in the oil-resistant composition may be 0.01% by weight or more, 0.03% by weight or more, 0.5% by weight or more, 1% by weight or more, 3% by weight or more, 5% by weight or more, 7% by weight or more, 10% by weight or more, 20% by weight or more, 30% by weight or more, or 95% by weight or less, 90% by weight or less, 80% by weight or less, 70% by weight or less, 60% by weight or less, 50% by weight or less, 40% by weight or less, 30% by weight or less, 20% by weight or less, 10% by weight or less, 5% by weight or less, 3% by weight or less, or 2% by weight or less. 【0105】The amount of hydrocarbon group-containing polymer (1) may be 3% by weight or more, 5% by weight or more, 10% by weight or more, 20% by weight or more, 30% by weight or more, 40% by weight or more, or 45% by weight or more, preferably 10% by weight or more, and may also be 95% by weight or less, 90% by weight or less, 80% by weight or less, 70% by weight or less, 60% by weight or less, 50% by weight or less, 40% by weight or less, 30% by weight or less, 20% by weight or less, 10% by weight or less, 5% by weight or less, 3% by weight or less, or 2% by weight or less. 【0106】 [(2) Crosslinking agent component] The oil-resistant composition in this disclosure contains a crosslinking agent component (2). The crosslinking agent component (2) may be added to the oil-resistant composition after polymerization to obtain a hydrocarbon-containing polymer (1). 【0107】 The crosslinking agent component (2) in the oil-resistant composition can cure the hydrocarbon-containing polymer (1). The crosslinking agent component (2) may be an active hydrogen-reactive compound or an active hydrogen-containing compound that reacts with the active hydrogen or active hydrogen-reactive groups present in the hydrocarbon-containing polymer (1). The crosslinking agent component (2) is a compound that can crosslink with the hydrocarbon-containing polymer. 【0108】 The crosslinking agent component may be at least one selected from the group consisting of aldehyde compounds, organometallic compounds, isocyanate compounds, and epoxy compounds. These may be used alone or in combination of two or more. 【0109】 Examples of active hydrogen-containing compounds that can react with crosslinking agent components include hydroxyl group-containing compounds, amino group-containing compounds, carboxyl group-containing compounds, ketone group-containing compounds, hydrazide compounds, melamine compounds, and urea-based compounds. 【0110】 The oil-resistant composition may contain a compound in which a hydrocarbon-containing polymer (1) is crosslinked by a crosslinking agent component (2). The hydrocarbon-containing polymer (1) may have a structure in which a polymer chain constituting the hydrocarbon-containing polymer (1) and another polymer constituting the hydrocarbon-containing polymer (1) are crosslinked by the crosslinking agent component (2). 【0111】[Aldehyde Compounds] Aldehyde compounds are compounds that have an aldehyde group in their molecule. Aldehyde compounds may be polyaldehyde compounds having two or more aldehyde groups. 【0112】 The aldehyde compound may be an aldehyde compound having a hydrocarbon group having 1 to 20 carbon atoms. The hydrocarbon group may be linear, branched, or cyclic. The hydrocarbon group may be an aliphatic hydrocarbon group or an aromatic hydrocarbon group. The hydrocarbon group having 1 to 20 carbon atoms may be a hydrocarbon group having 2 to 10 carbon atoms, preferably 2 to 6 carbon atoms, and more preferably 2 to 4 carbon atoms. 【0113】 Aldehyde compounds include, for example, monoaldehydes such as formaldehyde, acetaldehyde, propionaldehyde, butyraldehyde, isobutyraldehyde, pentylaldehyde, isopentylaldehyde, hexylaldehyde, 2-ethylhexylaldehyde, methylglyoxal, and cyclohexylaldehyde; aromatic aldehydes or heterocyclic aldehydes such as benzaldehyde, o-tolualdehyde, p-tolualdehyde, m-tolualdehyde, p-hydroxybenzaldehyde, salicylaldehyde, and furfural; and hydroxyl group-containing aldehydes such as glycolaldehyde and glyoxylic acid. Examples include dialdehydes such as glyoxal, malondialdehyde, succinidaldehyde, glutardialdehyde, maleidaldehyde, heptanedial, octanedial, nonanedial, benzenetricarboxylaldehyde, and phthalidaldehyde; and polyaldehydes such as dialdehyde starch and polyacrolein. 【0114】 The aldehyde compound may include the polymers (e.g., polymers or cyclic trimers) mentioned above. 【0115】 The aldehyde compound is preferably an aliphatic aldehyde compound containing an aliphatic hydrocarbon, such as glyoxal, methylglyoxal, propanal, glycolaldehyde, or glyoxylic acid. The aldehyde compound is preferably an aldehyde compound containing two or more carbonyl groups (-C(=O)-). Examples of such aldehyde compounds include glyoxal and methylglyoxal. 【0116】 [Organometallic Compounds] Organometallic compounds are compounds that can react with functional groups such as hydroxyl groups, carboxyl groups, and / or amino groups. Organometallic compounds are compounds having a structure in which an organic group is bonded to a polyvalent metal. The organic group may be a monovalent or polyvalent group containing carbon atoms and / or oxygen atoms. The bond of the organic group to the polyvalent metal is not particularly limited and may be a covalent bond, an ionic bond, or a coordinate bond formed by coordination of a chelate compound, etc. 【0117】 Polyvalent metals refer to metals with two or more valent values. Examples of polyvalent metals include zirconium, titanium, magnesium, calcium, aluminum, iron, nickel, silicon, boron, zinc, copper, vanadium, chromium, and tin, with zirconium and titanium being preferred. 【0118】 Organic groups that bond to polyvalent metals include alkyl groups, alkoxy groups, acyl groups, carboxyl groups, and hydroxyl groups. 【0119】 The organometallic compounds are preferably organotitanium compounds, organozirconium compounds, or salts thereof. 【0120】 Specific examples of organotitanium compounds include, for example, titanium alkoxides or titanium orthoesters such as tetran-butyl titanate, tetraisopropyl titanate, butyl titanate dimer, tetra(2-ethylhexyl) titanate, and tetramethyl titanate; titanium chelates such as titanium acetylacetonate, titanium tetraacetylacetonate, polytitanium acetylacetonate, titanium octylene glycolate, titanium lactate, titanium triethanolamine, and titanium ethylacetoacetate; titanium acylates such as polyhydroxytitanium stearate; and salts of the organotitanium compounds listed above. 【0121】Specific examples of organozirconium compounds include, for example, zirconium alkoxides or zirconium orthoesters such as zirconium n-propionate and zirconium n-butyrate; zirconium chelates such as zirconium tetraacetylacetonate, zirconium monoacetylacetonate, zirconium bisacetylacetonate, and zirconium acetylacetonate bisethylacetoacetate; and titanium acylates such as zirconium stearate. 【0122】 Commercially available organometallic compounds may be used. Examples of organometallic compounds include Organix TC-310, Organix TC-300, Organix TC-315, Organix TC-335, Organix TC-400, Organix TC-510, Organix ZC-126, Organix ZC-150, Organix ZC-162, Organix 540, and Organix ZC-700. 【0123】 [Isocyanate Compounds] Isocyanate compounds are compounds having isocyanate groups, preferably compounds having two or more isocyanate groups in one molecule. Isocyanate compounds can act as crosslinking agents. Examples of isocyanate compounds include aliphatic isocyanate compounds, alicyclic isocyanate compounds, aromatic aliphatic isocyanate compounds, aromatic isocyanate compounds, and derivatives of these isocyanate compounds. 【0124】Examples of aliphatic isocyanate compounds include trimethylene diisocyanate, tetramethylene diisocyanate, hexamethylene diisocyanate, pentamethylene diisocyanate, 1,2-propylene diisocyanate, 1,2-butylene diisocyanate, 2,3-butylene diisocyanate, 1,3-butylene diisocyanate, 2,4,4- or 2,2,4-trimethylhexamethylene diisocyanate, and 2,6-di These include aliphatic diisocyanates such as socyanatomethylcaproate, and aliphatic triisocyanates such as lysine ester triisocyanate, 1,4,8-triisocyanatooctane, 1,6,11-triisocyanatoundecane, 1,8-diisocyanato-4-isocyanatomethyloctane, 1,3,6-triisocyanatohexane, and 2,5,7-trimethyl-1,8-diisocyanato-5-isocyanatomethyloctane. 【0125】 Examples of alicyclic isocyanate compounds include alicyclic diisocyanates and alicyclic triisocyanates. Specific examples of alicyclic polyisocyanates include 1,3-cyclopentene diisocyanate, 3-isocyanatomethyl-3,5,5-trimethylcyclohexyl isocyanate (isophorone diisocyanate), 1,3,5-triisocyanatocyclohexane, 4,4'methylenebis(cyclohexyl isocyanate), and 1,3-bis(isocyanatomethyl)cyclohexane. 【0126】 Examples of aroliphatic isocyanate compounds include aroliphatic diisocyanates and aroliphatic triisocyanates. Specific examples of aroliphatic polyisocyanates include 1,3- or 1,4-xylylene diisocyanate or mixtures thereof, 1,3- or 1,4-bis(1-isocyanato-1-methylethyl)benzene (tetramethylxylylene diisocyanate) or mixtures thereof, and 1,3,5-triisocyanatomethylbenzene. 【0127】Examples of aromatic isocyanate compounds include aromatic diisocyanates, aromatic triisocyanates, and aromatic tetraisocyanates. Specific examples of aromatic polyisocyanates include m-phenylenediisocyanate, p-phenylenediisocyanate, 4,4'-diphenyldiisocyanate, 1,5-naphthalenediisocyanate, 2,4'- or 4,4'-diphenylmethanediisocyanate or mixtures thereof, 2,4- or 2,6-tolylenediisocyanate or mixtures thereof, triphenylmethane-4,4',4''-triisocyanate, and 4,4'-diphenylmethane-2,2',5,5'-tetraisocyanate, etc. 【0128】 Examples of isocyanate compound derivatives include various derivatives of the polyisocyanate compounds mentioned above, such as dimers, trimers, biuretes, allophanates, carbodiimides, uretodiones, uretoimines, isocyanurates, and iminooxadiazinediones. 【0129】 These isocyanate compounds can be used individually or in combination of two or more. It is preferable to use blocked isocyanate compounds (blocked isocyanates), which are compounds in which the isocyanate group of an isocyanate compound is blocked with a blocking agent. Blocked isocyanate compounds are preferred because they are relatively stable in aqueous solutions and can be used in the same aqueous solutions as oil-resistant compositions. 【0130】 Blocking agents sequester free isocyanate groups. Blocked isocyanate compounds can be easily reacted with hydroxyl groups by heating them to, for example, 100°C or higher, such as 130°C or higher, which regenerates the isocyanate groups. Examples of blocking agents include phenolic compounds, lactam compounds, aliphatic alcohol compounds, oxime compounds, and pyrazole compounds. Isocyanate compounds can be used alone or in combination of two or more. 【0131】[Epoxy Compounds] Epoxy compounds are compounds that have epoxy groups. The number of epoxy groups in an epoxy compound is not particularly limited, but it is preferable that it has two or more epoxy groups. 【0132】 Examples of epoxy compounds are not particularly limited, but may include epoxy compounds obtained by the reaction of a reactive compound having a hydroxyl group, an amino group, or a carboxyl group with an epoxy group (or glycidyl group) introduced compound such as epichlorohydrin. 【0133】 Examples of the above-mentioned reactive compounds include polyols such as ethylene glycol and glycerin, polycarboxylic acids such as phthalic acid and terephthalic acid, and polyamines such as ethylenediamine and diethylenetriamine. 【0134】 Examples of epoxy compounds are not particularly limited, but include glycidyl ethers such as ethylene glycol glycidyl ether, glycerol polyglycidyl ether, diglycerol polyglycidyl ether, sorbitol polyglycidyl ether, polyglycerol polyglycidyl ether, bisphenol A diglycidyl ether, bisphenol S diglycidyl ether, novolac glycidyl ether, polyethylene glycol diglycidyl ether, and brominated bisphenol A diglycidyl ether; glycidyl esters such as hexahydrophthalate glycidyl ester and dimer acid glycidyl ester; and glycidylamines such as triglycidyl isocyanurate, glycidyl hydantoin, tetraglycidyldiaminodiphenylmethane, triglycidylparaaminophenol, triglycidylmetaaminophenol, diglycidylaniline, diglycidyltoluidine, tetraglycidylmetaxyldiamine, diglycidyltribromaniline, and tetraglycidylbisaminomethylcyclohexane. 【0135】The epoxy compound may be an epoxy resin, and examples include aliphatic epoxy resins, alicyclic epoxy resins, glycidyl ether epoxy resins (bisphenol A type, bisphenol F type, etc.), glycidyl ester epoxy resins, glycidylamine epoxy resins, naphthalene-type epoxy resins, isocyanurate-type epoxy resins, and the like. 【0136】 The crosslinking agent component (2) may be any compound other than those listed above, for example, a chloromethyl group-containing compound, a carboxyl group-containing compound, or a hydrazide compound. Specific examples of ketone group-containing compounds include (poly)diacetone acrylamide and diacetone alcohol. Specific examples of hydrazide compounds include hydrazine, carbohydrazide, and adipic acid hydrazide. Specific examples of melamine compounds include melamine resin and methyl etherified melamine resin. Specific examples of urea-based compounds include dimethylol dihydroxyethylene urea (DMDHEU) and dimethyl dihydroxyethylene urea. The catalyst may include organic acids, metal chlorides, metal nitrates, etc. 【0137】 [Amount of Crosslinking Agent Component (2)] The amount of crosslinking agent component (2) may be 0.1 parts by weight or more, 1 part by weight or more, 3 parts by weight or more, 5 parts by weight or more, 10 parts by weight or more, 15 parts by weight or more, or 20 parts by weight or more per 100 parts by weight of hydrocarbon-containing polymer (1), and may also be 95 parts by weight or less, 90 parts by weight or less, 85 parts by weight or less, 80 parts by weight or less, 70 parts by weight or less, 60 parts by weight or less or 50 parts by weight or less, 40 parts by weight or less, 30 parts by weight or less, 20 parts by weight or less, 10 parts by weight or less, or 5 parts by weight or less. The amount of crosslinking agent component (2) is preferably 0.1 parts by weight or more and 20 parts by weight or less, more preferably 0.1 parts by weight or more and 10 parts by weight or less per 100 parts by weight of hydrocarbon-containing polymer (1). 【0138】The amount of crosslinking agent component (2) may be 0.1% by weight or more, 0.3% by weight or more, 0.5% by weight or more, 1% by weight or more, 3% by weight or more, 5% by weight or more, 10% by weight or more, 20% by weight or more, 30% by weight or more in the oil-resistant composition, or 90% by weight or less, 80% by weight or less, 70% by weight or less, 60% by weight or less, 50% by weight or less, 40% by weight or less, 30% by weight or less, 20% by weight or less, 10% by weight or less, 5% by weight or less, 3% by weight or less, or 2% by weight or less. 【0139】 The amount of the crosslinking agent component (2) may be 10% by weight or more, 12% by weight or more, 16% by weight or more, 20% by weight or more, 24% by weight or more, 28% by weight or more, 32% by weight or more, or 36% by weight or more, relative to the total amount of the hydrocarbon-containing polymer (1) and the crosslinking agent component (2), and may also be 70% by weight or less, 65% by weight or less, 60% by weight or less, 55% by weight or less, 52% by weight or less, 48% by weight or less, 46% by weight or less, 42% by weight or less, 40% by weight or less, or 36% by weight or less, for example, 12% by weight or more and 52% by weight or less. 【0140】 [(3) Water-soluble polymers] The oil-resistant composition in this disclosure may also contain water-soluble polymers (3). 【0141】 The weight-average molecular weight of the water-soluble polymer (3) may be 1000 or more, 3000 or more, 5000 or more, 10000 or more, 30000 or more, 100000 or more, 300000 or more, or 500000 or more, and may also be 1000000 or less, 750000 or less, 500000 or less, 3000000 or less, 100000 or less, 75000 or less, 50000 or less, 30000 or less, 10000 or less, 5000 or less, or 3000 or less. 【0142】 The water-soluble polymer (3) may be hydrophobically modified. The hydrophobically modified water-soluble polymer (3) may mean a compound modified with, for example, one or more, two or more, three or more, five or more, ten or more, thirty or more, or fifty or more hydrophobic functional groups (e.g., hydrocarbon groups having 6 or more, 10 or more, 12 or more, 15 or more, or 18 or more carbon atoms). 【0143】The water-soluble polymer (3) may be a polycarboxylic acid. The water-soluble polymer (2) may have other acidic functional groups. 【0144】 Examples of water-soluble polymers (3) include polysaccharides, synthetic polyols, polyamines, polyamides, polyethers, etc. Preferably, and more preferably, are polysaccharides or synthetic polyols. 【0145】 The water-soluble polymer (3) is preferably a polyol, and may be a polysaccharide or a synthetic polyol. The number of hydroxyl groups in the polyol may be 10 or more, 15 or more, 30 or more, 50 or more, or 100 or more, and may also be 3000 or less, 1000 or less, 750 or less, 500 or less, 300 or less, 100 or less, 50 or less, 30 or less, or 20 or less. 【0146】 Polysaccharides may be acidic polysaccharides, neutral sugars, and / or basic sugars, but are preferably neutral. Acidic polysaccharides are generally polysaccharides having a carboxyl group (-COOH), etc. Specific examples of acidic polysaccharides are carrageenan, pectin, gum arabic, xanthan gum, gellan gum, agar, and tragacanth gum. Neutral polysaccharides are polysaccharides that are electrically neutral. Specific examples of neutral polysaccharides are tamarind seed gum, guar gum, locust bean gum, starch, and pullulan. Basic polysaccharides are polysaccharides having an amino group (-NH2), etc. Specific examples of basic polysaccharides are chitosan. Specific examples of polysaccharides include starch, xanthan gum, karaya gum, gellan gum, guar gum, pectin, tamarind gum, carrageenan, chitosan, gum arabic, locust bean gum, cellulose, alginic acid, agar, dextran, and pullulan. 【0147】As the polysaccharide, starch is preferred. The starch may be unmodified starch or modified starch. The starch may be modified starch that has undergone at least one modification, such as esterification modification, hydrophobization modification, etherification modification, oxidation modification, alkali modification, enzyme modification, and bleach modification. Examples of modified starches include acetylated adipic acid crosslinked starch, acetylated oxidized starch, acetylated phosphate crosslinked starch, alkenyl succinate esterified starch, acetate starch, oxidized starch, hydroxyalkylated starch (alkyl group having 2 to 40 or 2 to 10 carbon atoms, particularly 2 or 3 carbon atoms), hydroxyalkylated phosphate crosslinked starch (alkyl group having 2 to 40 or 2 to 10 carbon atoms, particularly 2 or 3 carbon atoms), phosphate crosslinked starch, phosphorylated starch, phosphate monoesterified phosphate crosslinked starch, acid-modified starch, alkali-treated starch, enzyme-treated starch, bleach-treated starch, and cationized starch (quaternary ammonium starch). Dextrin, which is starch that has been reduced in molecular weight by chemical or enzymatic methods, can also be mentioned. The starch may be pregelatinized starch. Pregelatinized starch is starch in which the hydrogen bonds between sugar chains have been broken, leaving the sugar chains free. 【0148】 Synthetic polyols are synthetic polyols having a plurality of hydroxyl groups (for example, 10 or more, 50 or more, 100 or more, or 500 or more) in their molecule, and preferably include polyglycerin, polyvinyl alcohol, hydroxyethyl (meth)acrylate polymer, hydroxypropyl (meth)acrylate polymer, hydroxybutyl (meth)acrylate polymer, polyvinyl alcohol, and others, with polyvinyl alcohol being particularly preferable. 【0149】Specific examples of water-soluble polymers (3) include polysaccharides such as starch, pullulan, amylose, cellulose, cellulose derivatives, carrageenan, guar gum, chitin, chitosan, locust bean gum, kappa-carrageenan, iota-carrageenan, isomaltodextrin, gellan gum, and tamarind seed gum; synthetic polyols such as polyglycerin, polyvinyl alcohol, hydroxyethyl (meth)acrylate polymer, hydroxypropyl (meth)acrylate polymer, hydroxybutyl (meth)acrylate polymer, and polyvinyl alcohol; and polyethyl Examples include polyamines such as lenimine, polyvinylamine, and polyallylamine; polyamides such as polyvinylpyrrolidone, polyacrylamide, poly(N,N-dimethylacrylamide), poly(N-vinylacetamide), poly-N-isopropylacrylamide, polyoxazolines (e.g., poly(2-methyl-2-oxazoline), poly(2-ethyl-2-oxazoline), poly(2-propyl-2-oxazoline)), and polyamideimides; and polyethers such as polyethylene glycol, polypropylene glycol, and polyvinyl methyl ether. 【0150】 [Amount of water-soluble polymer (3)] The amount of water-soluble polymer (3) may be 30 parts by weight or more, 100 parts by weight or more, 300 parts by weight or more, 400 parts by weight or more, 500 parts by weight or more, 750 parts by weight or more, 1000 parts by weight or more, 1500 parts by weight or more, or 2000 parts by weight or more, per 100 parts by weight of hydrocarbon-containing polymer (1), and may also be 5000 parts by weight or less, 4500 parts by weight or less, 4000 parts by weight or less, 3500 parts by weight or less, 3000 parts by weight or less, 2500 parts by weight or less, 2000 parts by weight or less, 1500 parts by weight or less, 1200 parts by weight or less, 1000 parts by weight or less, 750 parts by weight or less, 500 parts by weight or less, or 300 parts by weight or less. 【0151】The amount of water-soluble polymer (3) may be 1% by weight or more, 3% by weight or more, 5% by weight or more, 7% by weight or more, 10% by weight or more, 15% by weight or more, 20% by weight or more, 30% by weight or more, 40% by weight or more, 50% by weight or more, 60% by weight or more, 70% by weight or more, 80% by weight or more, 90% by weight or more, 95% by weight or more, or 97% by weight or more, and may also be 99.9% by weight or less, 99% by weight or less, 95% by weight or less, 90% by weight or less, 80% by weight or less, 70% by weight or less, 60% by weight or less, 50% by weight or less, 40% by weight or less, 30% by weight or less, 20% by weight or less, or 18% by weight or less. 【0152】 The amount of water-soluble polymer (3) may be 60% or more, 70% or more, 80% or more, 90% or more, 95% or more, or 97% or more by weight, relative to the total amount of hydrocarbon-containing polymer (1), crosslinking agent component (2), and water-soluble polymer (3), and may also be 99.9% or less by weight, 99% or less by weight, 95% or less by weight, 90% or less by weight, 80% or less by weight, 70% or less by weight, 60% or less by weight, 50% or less by weight, 40% or less by weight, 30% or less by weight, 20% or less by weight, 17% or less by weight, or 15% or less by weight. 【0153】 [Liquid Media] The oil-resistant composition may contain a liquid media. The liquid media is water, an organic solvent, or a mixture of water and an organic solvent. Preferably, it is a mixture of water and an organic solvent. By including an organic solvent, good water repellency, slip resistance, and storage stability can be achieved. 【0154】Examples of organic solvents include esters (e.g., esters having 2 to 40 carbon atoms, specifically ethyl acetate and butyl acetate), ketones (e.g., ketones having 2 to 40 carbon atoms, specifically methyl ethyl ketone and diisobutyl ketone), alcohols (e.g., alcohols having 1 to 40 carbon atoms, specifically isopropyl alcohol), aromatic solvents (e.g., toluene and xylene), and petroleum solvents (e.g., alkanes having 5 to 10 carbon atoms, specifically naphtha and kerosene). The organic solvent is preferably a water-soluble organic solvent. The water-soluble organic solvent may contain compounds having at least one hydroxyl group (e.g., polyhydric alcohols such as alcohols and glycol-based solvents, ether forms of polyhydric alcohols (e.g., monoether forms)). These may be used individually or in combination of two or more. 【0155】 [Amount of liquid medium] The amount of liquid medium may be 40% by weight or more, 50% by weight or more, 60% by weight or more, 70% by weight or more, 80% by weight or more, 90% by weight or more, 95% by weight or more, or 97% by weight or more relative to the oil-resistant composition, and may also be 99.9% by weight or less, 99% by weight or less, 95% by weight or less, 90% by weight or less, 80% by weight or less, 70% by weight or less, 60% by weight or less, or 50% by weight or less. 【0156】 The amount of organic solvent may be 0.5% or more by weight, 1% or more by weight, 2% or more by weight, 3% or more by weight, 5% or more by weight, 7.5% or more by weight, 10% or more by weight, 12.5% ​​or more by weight, 15% or more by weight, or 20% or more by weight relative to the oil-resistant composition, and may also be 75% or less by weight, 50% or less by weight, 40% or less by weight, 30% or less by weight, 25% or less by weight, 20% or less by weight, 15% or less by weight, 10% or less by weight, or 5% or less by weight. 【0157】 The amount of organic solvent may be 1% by weight or more, 3% by weight or more, 5% by weight or more, 10% by weight or more, 20% by weight or more, 30% by weight or more, or 40% by weight or more relative to the liquid medium, and may also be 55% by weight or less, 45% by weight or less, 35% by weight or less, 25% by weight or less, 15% by weight or less, 12.5% ​​by weight or less, 7.5% by weight or less, or 5.0% by weight or less. 【0158】The amount of organic solvent may be 1 part by weight or more, 3 parts by weight or more, 5 parts by weight or more, 10 parts by weight or more, 20 parts by weight or more, 30 parts by weight or more, 40 parts by weight or more, or 50 parts by weight or more per 100 parts by weight of hydrocarbon-containing polymer (1), and may also be 200 parts by weight or less, 175 parts by weight or less, 150 parts by weight or less, 125 parts by weight or less, 100 parts by weight or less, 80 parts by weight or less, 60 parts by weight or less, 40 parts by weight or less, 20 parts by weight or less, or 10 parts by weight or less. 【0159】 The amount of organic solvent may be 0.5 parts by weight or more, 1 part by weight or more, 1.5 parts by weight or more, 3 parts by weight or more, 5 parts by weight or more, 10 parts by weight or more, 15 parts by weight or more, 20 parts by weight or more, 30 parts by weight or more, or 40 parts by weight or more, per 100 parts by weight of water, or 100 parts by weight or less, 75 parts by weight or less, 50 parts by weight or less, 25 parts by weight or less, 10 parts by weight or less, or 5 parts by weight or less. 【0160】 [Silicone] The oil-resistant composition in this disclosure may contain silicone (polyorganosiloxane). By including silicone, it is possible to obtain good liquid repellency in addition to good texture and durability. 【0161】 As the silicone, known silicones can be used, and examples of silicones include polydimethylsiloxane and modified silicones (amino-modified, epoxy-modified, carboxy-modified, methylhydrogen silicone, etc.). The silicone may also be a silicone wax having waxy properties. These may be used alone or in combination of two or more. 【0162】 The weight-average molecular weight of the silicone may be 1,000 or more, 10,000 or more, or 50,000 or more, and may also be 500,000 or less, 2,500,000 or less, 100,000 or less, or 50,000 or less. 【0163】[Amount of Silicone] The amount of silicone may be 0.1 parts by weight or more, 1 part by weight or more, 3 parts by weight or more, 5 parts by weight or more, 10 parts by weight or more, 15 parts by weight or more, 20 parts by weight or more, 50 parts by weight or more, 75 parts by weight or more, or 100 parts by weight or more per 100 parts by weight of hydrocarbon-containing polymer (1), or 500 parts by weight or less, 300 parts by weight or less, 200 parts by weight or less, 100 parts by weight or less, 50 parts by weight or less, 40 parts by weight or less, 30 parts by weight or less, 20 parts by weight or less, 10 parts by weight or less, or 5 parts by weight or less. 【0164】 [Wax] The oil-resistant composition in this disclosure preferably contains wax in addition to the hydrocarbon-containing polymer (1). By including wax, it is possible to obtain a good combination of water repellency, slip resistance, and storage stability. The oil-resistant composition in this disclosure may contain both silicone and wax, or it may contain only one of silicone and wax. 【0165】Examples of waxes include paraffin wax, microcrystalline wax, Fischer-Tropsch wax, polyolefin wax (polyethylene wax, polypropylene wax, etc.), oxidized polyolefin wax, animal and plant waxes, and mineral waxes. Paraffin wax is preferred. Specific examples of compounds constituting the wax are normal alkanes (e.g., tricosane, tetracosane, pentacosane, hexacosane, heptacosane, octacosane, nonacosane, triacontane, hentriacontane, dotriacontane, tritriacontane, tetratriacontane, pentatriacontane, hexatriacontane) and normal alkenes (e.g., 1-eicosene, 1-docosene, 1-tricosene, 1-tetracosene, 1-pentacosene, 1-hexacosene, 1-heptacosene, 1-octacosene, nonacosane, triacontane, hentriacontane, dotriacontane, tritriacontane, tetratriacontane, pentatriacontane, hexatriacontane). The number of carbon atoms in the compounds constituting the wax is preferably 20 to 60, for example, 25 to 45. The molecular weight of the wax may be 200 to 2000, for example, 250 to 1500 or 300 to 1000. These may be used alone or in combination of two or more. 【0166】 The melting point of the wax may be 50°C or higher, 55°C or higher, 60°C or higher, 65°C or higher, or 70°C or higher, preferably 55°C or higher, more preferably 60°C or higher, and may also be 120°C or lower, 100°C or lower, 80°C or lower, 75°C or lower, 70°C or lower, or 65°C or lower. The melting point of the wax is measured in accordance with JIS K 2235-1991. 【0167】 [Amount of wax] The amount of wax may be 0.1 parts by weight or more, 1 part by weight or more, 3 parts by weight or more, 5 parts by weight or more, 10 parts by weight or more, 15 parts by weight or more, or 20 parts by weight or more per 100 parts by weight of hydrocarbon-containing polymer (1), or it may be 50 parts by weight or less, 40 parts by weight or less, 30 parts by weight or less, 20 parts by weight or less, 10 parts by weight or less, or 5 parts by weight or less. 【0168】[Organic Acids] The oil-resistant composition may contain organic acids. Known organic acids can be used. Preferred organic acids include carboxylic acids, sulfonic acids, sulfinic acids, etc., with carboxylic acids being particularly preferred. Examples of carboxylic acids include formic acid, acetic acid, propionic acid, butyric acid, oxalic acid, succinic acid, glutaric acid, adipic acid, malic acid, citric acid, etc., with formic acid or acetic acid being particularly preferred. In this disclosure, one organic acid may be used, or two or more may be used in combination. For example, formic acid and acetic acid may be used in combination. 【0169】 [Amount of Organic Acid] The amount of organic acid may be 0.1 parts by weight or more, 1 part by weight or more, 3 parts by weight or more, 5 parts by weight or more, 10 parts by weight or more, 15 parts by weight or more, or 20 parts by weight or more per 100 parts by weight of hydrocarbon-containing polymer (1), or it may be 50 parts by weight or less, 40 parts by weight or less, 30 parts by weight or less, 20 parts by weight or less, 10 parts by weight or less, or 5 parts by weight or less. The amount of organic acid may be adjusted so that the pH of the oil-resistant composition is 3 to 10, for example 5 to 9, and particularly 6 to 8. The oil-resistant composition may be acidic (pH 7 or less, for example 6 or less). 【0170】 [Dispersant] The oil-resistant composition of this disclosure may or may not contain a dispersant. In particular, when monomer (c) is present, the water dispersibility of the hydrocarbon-containing polymer (1) is improved, so the amount of dispersant can be reduced. 【0171】 The dispersant is selected from organic dispersants and inorganic dispersants. There may be at least one of them. The dispersant may be non-anionic and may be at least one selected from nonionic dispersants, cationic dispersants, amphoteric dispersants, and inorganic dispersants. The oil-resistant composition does not have to contain anionic dispersants. The dispersant may also contain dispersants other than fatty acid esters. 【0172】 The dispersant may be either an organic dispersant or an inorganic dispersant, or a combination of both. 【0173】An organic dispersant may be used as the dispersant. The organic dispersant can be classified into nonionic dispersants, anionic dispersants, cationic dispersants, and amphoteric dispersants, and the organic dispersant may mean a surfactant. 【0174】 The dispersant may be a fluorine-free dispersant. 【0175】 [Nonionic Dispersant] The dispersant may contain a nonionic dispersant. The nonionic dispersant may be a nonionic surfactant. 【0176】 The nonionic dispersant may be of low molecular weight or high molecular weight. The molecular weight may be 100 or more, 500 or more, 1000 or more, 2000 or more, 4000 or more, or 6000 or more, and may also be 100000 or less, 50000 or less, 10000 or less, 7500 or less, 5000 or less, 2500 or less, 1000 or less, 750 or less, or 250 or less. 【0177】 Examples of the nonionic dispersant include ether, ester, ester ether, alkanolamide, polyol, and amine oxide. 【0178】 An example of the ether is a compound having an oxyalkylene group (preferably a polyoxyethylene group). 【0179】 An example of the ester is an ester of an alcohol and a fatty acid. Examples of the alcohol are 1-6 valent (especially 2-5 valent) alcohols having 1-50 carbon atoms (especially 10-30 carbon atoms) (e.g., aliphatic alcohols). Examples of the fatty acid are saturated or unsaturated fatty acids having 2-50 carbon atoms, especially 5-30 carbon atoms. 【0180】 An example of the ester ether is a compound obtained by adding an alkylene oxide (especially ethylene oxide) to an ester of an alcohol and a fatty acid. Examples of the alcohol are 1-6 valent (especially 2-5 valent) alcohols having 1-50 carbon atoms (especially 3-30 carbon atoms) (e.g., aliphatic alcohols). Examples of the fatty acid are saturated or unsaturated fatty acids having 2-50 carbon atoms, especially 5-30 carbon atoms. 【0181】Examples of alkanolamides are formed from fatty acids and alkanolamines. Alkanolamides may be monoalkanolamides or dialkanolamides. Examples of fatty acids are saturated or unsaturated fatty acids having 2 to 50 carbon atoms, particularly 5 to 30 carbon atoms. Alkanolamines may be alkanols having 2 to 50 carbon atoms, particularly 5 to 30 carbon atoms, having 1 to 3 amino groups and 1 to 5 hydroxyl groups. 【0182】 The polyol may be a divalent to pentavalent alcohol having 10 to 30 carbon atoms. The amine oxide may be an oxide of an amine (secondary amine or preferably tertiary amine) (for example, having 5 to 50 carbon atoms). 【0183】 The nonionic dispersant is preferably a nonionic dispersant having an oxyalkylene group (preferably a polyoxyethylene group). The number of carbon atoms in the alkylene group of the oxyalkylene group is preferably 2 to 10. The number of oxyalkylene groups in the molecule of the nonionic dispersant is generally preferably 2 to 100. 【0184】 The nonionic dispersant is selected from the group consisting of ethers, esters, ester ethers, alkanolamides, polyols, and amine oxides, and is preferably a nonionic dispersant having an oxyalkylene group. 【0185】 Nonionic dispersants may be alkylene oxide adducts of linear and / or branched aliphatic (saturated and / or unsaturated) groups, polyalkylene glycol esters of linear and / or branched fatty acids (saturated and / or unsaturated), polyoxyethylene (POE) / polyoxypropylene (POP) copolymers (random copolymers or block copolymers), alkylene oxide adducts of acetylene glycol, etc. Among these, those in which the structure of the alkylene oxide adduct and the polyalkylene glycol portion is polyoxyethylene (POE), polyoxypropylene (POP), or POE / POP copolymer (which may be random copolymers or block copolymers) are preferred. Furthermore, nonionic dispersants are preferably structured without aromatic groups. 【0186】Nonionic dispersants are given by formula: R 1 O-(CH ２ CH ２ O) p -(R 2 O) q -R 3 [In the formula, R 1 R is an alkyl group having 1 to 22 carbon atoms, or an alkenyl group or acyl group having 2 to 22 carbon atoms. 2 Each of them is independently identical or distinct, an alkylene group having 3 or more carbon atoms (for example, 3 to 10), R 3 The compound may be represented by [where p is a hydrogen atom, an alkyl group having 1 to 22 carbon atoms, or an alkenyl group having 2 to 22 carbon atoms, p is a number of 2 or more, and q is 0 or a number of 1 or more]. 【0187】 R 1 The carbon atoms have 8 to 20 carbon atoms, and are more preferably 10 to 18 carbon atoms. 1 Preferred specific examples include the lauryl group, tridecyl group, and oleyl group. 2 Examples include propylene groups and butylene groups. In nonionic dispersants, p may be a number of 3 or more (e.g., 5 to 200). q may be a number of 2 or more (e.g., 5 to 200). That is, -(R 2 O) q - may form a polyoxyalkylene chain. The nonionic dispersant may be a polyoxyethylene alkyl ether containing a hydrophilic polyoxyethylene chain and a hydrophobic oxyalkylene chain (particularly a polyoxyalkylene chain) in the center. Examples of hydrophobic oxyalkylene chains include oxypropylene chains, oxybutylene chains, and styrene chains, but oxypropylene chains are preferred among them. 【0188】 Specific examples of nonionic dispersants include ethylene oxide and hexylphenol, isooctatylphenol, hexadecanol, oleic acid, and alkanes (C). １２ -C １６ ) Thiol, sorbitan monofatty acid (C ７ -C １９ ) or alkyl (C １２ -C １８This includes condensation products with amines, sorbitan fatty acid esters, glycerin fatty acid esters, sucrose fatty acid esters, propylene glycol fatty acid esters, lecithin derivatives, and the like. 【0189】 The proportion of polyoxyethylene blocks can be 5 to 80% by weight, for example 30 to 75% by weight, and particularly 40 to 70% by weight, relative to the molecular weight of the nonionic dispersant (copolymer). The average molecular weight of the nonionic dispersant is generally 300 to 5,000, for example 500 to 3,000. The nonionic dispersant may be a single compound or a mixture of two or more compounds. The nonionic dispersant may be a mixture of compounds with an HLB (hydrophilic-hydrophobic balance) of less than 15 (particularly 5 or less) and compounds with an HLB of 15 or more. 【0190】 [Cationic Dispersant] The dispersant may contain a cationic dispersant. The cationic dispersant may be a cationic surfactant. The cationic dispersant may be of low molecular weight (e.g., molecular weight 2000 or less, particularly 1000 or less) or of high molecular weight (e.g., molecular weight 2000 or more). The cationic dispersant may be a compound that does not have an amide group. 【0191】 The cationic dispersant may be of low molecular weight or high molecular weight. The molecular weight may be 100 or more, 500 or more, 1000 or more, 2000 or more, 4000 or more, or 6000 or more, and may also be 100000 or less, 50000 or less, 10000 or less, 7500 or less, 5000 or less, 2500 or less, 1000 or less, 750 or less, or 250 or less. 【0192】The cationic dispersant may be an amine salt, a quaternary ammonium salt, or an oxyethylene-added ammonium salt. Specific examples of cationic dispersants are not particularly limited, but include alkylamine salts, amino alcohol fatty acid derivatives, polyamine fatty acid derivatives, amine salt-type dispersants such as imidazoline, alkyltrimethylammonium salts, dialkyldimethylammonium salts, alkyldimethylbenzylammonium salts, pyridinium salts, alkylisoquinolinium salts, benzalkonium chloride, benzethonium chloride, and other quaternary ammonium salt-type dispersants. 【0193】 A preferred example of a cationic dispersant is R ２１ -N ＋ (-R ２２ ) (-R ２３ ) (-R ２４ ) X － [In the formula, R ２１ , R ２２ , R ２３ and R ２４ The compound is represented by [ ] where is a hydrocarbon group having 1 to 40 carbon atoms, and X is an anionic group. ２１ , R ２２ , R ２３ and -R ２４ Specific examples of X are alkyl groups (e.g., methyl group, butyl group, stearyl group, palmityl group). Specific examples of X are halogens (e.g., chlorine) and acids (e.g., hydrochloric acid, acetic acid). The cationic dispersant is particularly preferably a monoalkyltrimethylammonium salt (alkyl group with 4 to 40 carbon atoms). 【0194】 The cationic dispersant is preferably an ammonium salt. The cationic dispersant has the formula: R １ ｐ -N ＋ R ２ ｑ X － [In the formula, R １ is C12 or higher (for example, C １２ ~C ５０ ) linear and / or branched aliphatic (saturated and / or unsaturated) groups, R ２(CH) ３ , C ２ H ５ (particularly preferred), X is a halogen atom (e.g., C) １ ~C ４ The fatty acid base is , where p is 1 or 2, q is 2 or 3, and p + q = 4. It may be an ammonium salt represented by ]. １ The number of carbon atoms may be 12 to 50, for example, 12 to 30. 【0195】 Specific examples of cationic dispersants include dodecyltrimethylammonium acetate, trimethyltetradecylammonium chloride, hexadecyltrimethylammonium bromide, trimethyloctadecylammonium chloride, (dodecylmethylbenzyl)trimethylammonium chloride, benzyldodecyldimethylammonium chloride, methyldodecyldi(hydropolyoxyethylene)ammonium chloride, benzyldodecyldi(hydropolyoxyethylene)ammonium chloride, and N-[2-(diethylamino)ethyl]oleamide hydrochloride. 【0196】 [Anionic Dispersant] The dispersant may contain an anionic dispersant. The anionic dispersant may be an anionic surfactant. The dispersant does not have to contain an anionic dispersant. 【0197】 The anionic dispersant may be of low molecular weight or high molecular weight. The molecular weight may be 100 or more, 500 or more, 1000 or more, 2000 or more, 4000 or more, or 6000 or more, and may also be 100000 or less, 50000 or less, 10000 or less, 7500 or less, 5000 or less, 2500 or less, 1000 or less, 750 or less, or 250 or less. 【0198】Examples of anionic dispersants include alkyl ether sulfates, alkyl sulfates, alkenyl ether sulfates, alkenyl sulfates, olefin sulfonates, alkanesulfonates, saturated or unsaturated fatty acid salts, alkyl or alkenyl ether carboxylates, α-sulfone fatty acid salts, N-acyl amino acid type dispersants, phosphate mono or diester type dispersants, and sulfosuccinate esters. 【0199】 [Amphoteric Dispersant] The dispersant may contain an amphoteric dispersant. The amphoteric dispersant may be an amphoteric surfactant. 【0200】 The amphoteric dispersant may be of low molecular weight or high molecular weight. The molecular weight may be 100 or more, 500 or more, 1000 or more, 2000 or more, 4000 or more, or 6000 or more, and may also be 100000 or less, 50000 or less, 10000 or less, 7500 or less, 5000 or less, 2500 or less, 1000 or less, 750 or less, or 250 or less. 【0201】 Examples of amphoteric dispersants include alanines, imidazolinium betaines, amide betaines, and betaine acetate. Specifically, these include lauryl betaine, stearyl betaine, laurylcarboxymethylhydroxyethylimidazolinium betaine, lauryldimethylaminoacetic acid betaine, and fatty acid amidopropyldimethylaminoacetic acid betaine. 【0202】 [Inorganic Dispersant] The dispersant may contain an inorganic dispersant. 【0203】 The average primary particle size of the inorganic dispersant may be 5 nm or larger, 30 nm or larger, 100 nm or larger, 1 μm or larger, 10 μm or larger, or 25 μm or larger, and may also be 100 μm or smaller, 50 μm or smaller, 10 μm or smaller, 1 μm or smaller, 500 nm or smaller, or 300 nm or smaller. The average primary particle size can be measured, for example, by observation with a microscope (scanning electron microscope or transmission electron microscope). 【0204】Examples of inorganic dispersants include polyvalent metal phosphates such as tricalcium phosphate, magnesium phosphate, aluminum phosphate, zinc phosphate, and hydroxyapatite; carbonates such as calcium carbonate and magnesium carbonate; silicates such as calcium metasilicate; sulfates such as calcium sulfate and barium sulfate; and hydroxides such as calcium hydroxide, magnesium hydroxide, and aluminum hydroxide. 【0205】 [Amount of dispersant] The amount of dispersant may be 0.01 parts by weight or more, 0.1 parts by weight or more, 1 part by weight or more, 3 parts by weight or more, 5 parts by weight or more, 10 parts by weight or more, 15 parts by weight or more, 20 parts by weight or more, 50 parts by weight or more, 75 parts by weight or more, or 100 parts by weight or more, per 100 parts by weight of hydrocarbon-containing polymer (1), and may also be 500 parts by weight or less, 300 parts by weight or less, 200 parts by weight or less, 100 parts by weight or less, 30 parts by weight or less, 20 parts by weight or less, 10 parts by weight or less, 5 parts by weight or less, 3 parts by weight or less, or 1 part by weight or less. 【0206】 [Other Components] The oil-resistant composition may contain other components besides those listed above. Examples of other components include polysaccharides, paper strength enhancers, flocculants, yield enhancers, coagulants, binder resins, sizing agents, fillers, preservatives, antibacterial agents, deodorants, fragrances, etc. These may be used alone or in combination of two or more. In addition to the above components, other components may include other water-repellent and / or oil-repellent agents, water-resistant and / or oil-resistant agents, dispersants, softeners, flame retardants, paint fixatives, drying speed regulators, crosslinking agents, film-forming aids, compatibilizers, viscosity modifiers, pH adjusters, insecticides, penetrants, defoamers, shape-retaining agents, pigment clays, polymer dispersants, stain removers, enzymes such as cellulase, amylase, protease, lipase, and keratinase as fiber surface modifiers, and antifoaming agents. These may be used alone or in combination of two or more. 【0207】[Paper Strength Enhancers, Flocculants, Yield Enhancers, or Coagulants] Examples of paper strength enhancers, flocculants, yield enhancers, or coagulants include styrene polymers (styrene / maleic acid polymers, styrene / acrylic acid polymers), urea-formaldehyde polymers, polyethyleneimine, melamine-formaldehyde polymers, polyamidoamine-epichlorohydrin polymers, polyacrylamide polymers, polyamine polymers, polydiallyldimethylammonium chloride, alkylamine-epichlorohydrin condensates, alkylenedichloride-polyalkylene polyamine condensates, dicyandiamide-formaldehyde condensates, dimethyldiallylammonium chloride polymers, and olefin / maleic anhydride polymers. 【0208】 [Sizing agents] Examples of sizing agents include cellulose-reactive sizing agents, such as rosin-based sizing agents like rosin soap, rosin-based emulsions / dispersions, cellulose-reactive sizing agents, such as emulsions / dispersions of acid anhydrides like alkyl and alkenyl succinic anhydrides (ASA), alkenyl and alkyl ketene dimers (AKD) and polymers, and anionic, cationic and amphoteric polymers of ethylenically unsaturated monomers, such as copolymers of styrene and acrylate. 【0209】 [Amount of other components] The amount of each or total amount of other components may be 0.1 parts by weight or more, 1 part by weight or more, 3 parts by weight or more, 5 parts by weight or more, 10 parts by weight or more, 15 parts by weight or more, 20 parts by weight or more, 50 parts by weight or more, 75 parts by weight or more, or 100 parts by weight or more, per 100 parts by weight of hydrocarbon-containing polymer (1), and may also be 1000 parts by weight or less, 500 parts by weight or less, 300 parts by weight or less, 200 parts by weight or less, 100 parts by weight or less, 50 parts by weight or less, 40 parts by weight or less, 30 parts by weight or less, 20 parts by weight or less, 10 parts by weight or less, or 5 parts by weight or less. 【0210】<Manufacture of Oil-Resistant Agent Composition> The manufacturing method of the oil-resistant agent composition of the present disclosure is not limited, and may include a step of polymerizing monomer (a) in the presence of an organic solvent to obtain a polymer solution containing a hydrocarbon-containing polymer (1), and a step of volatilizing the organic solvent from the polymer solution and adding water. By this manufacturing method, the performance of the obtained oil-resistant agent composition can be improved. 【0211】 The volatile organic solvent may be the organic solvent described in [Polymerization Method] above, and particularly may be a highly volatile organic solvent having a boiling point lower than that of water. In particular, the step of obtaining the polymer may be solution polymerization, and particularly solution polymerization without using water as a solvent. The amount of the organic solvent used may be 30% by weight or more, 50% by weight or more, 75% by weight or more, 90% by weight or more, or 95% by weight or more in the polymerization solvent. 【0212】 The volatilization of the organic solvent may be carried out until the remaining amount of the organic solvent becomes 10% by weight or less, 5% by weight or less, 3% by weight or less, 1% by weight or less, or 0.1% by weight or less. 【0213】 After volatilization, other additives may be added in addition to water. By adding water after volatilization, an aqueous dispersion can be obtained. Such an aqueous dispersion can also be used as an oil-resistant agent composition. 【0214】 The crosslinking agent component (2) may be mixed with the obtained aqueous dispersion, or may be mixed with the polymer solution obtained before volatilizing the organic solvent. 【0215】 The water-soluble polymer (3) may be mixed with the obtained aqueous dispersion, or may be mixed with the polymer solution obtained before volatilizing the organic solvent. 【0216】To ensure the oil-resistant composition exhibits high water repellency, it is preferable to subject the oil-resistant composition to ultrasound (ultrasonic treatment). It is preferable to perform the ultrasonic treatment immediately before applying it to the object to be treated. For example, the oil-resistant composition is applied to the object to be treated 1 minute to 1 hour after ultrasonic treatment. Ultrasonic treatment can be performed by applying ultrasound to the oil-resistant composition. There are no particular restrictions on the ultrasonic generator, but an output of 500W or more, for example 500 to 2000W, is preferable for efficient mixing. The ultrasonic treatment time may be 0.5 to 60 minutes. For example, a uniform oil-resistant composition can be obtained by treating it for 10 minutes with a 500W ultrasonic generator. 【0217】 To obtain a polymer aqueous dispersion with excellent stability during storage, it is desirable to polymerize the monomers by micronizing them in water using an emulsifying device that can impart strong crushing energy, such as a high-pressure homogenizer or an ultrasonic homogenizer. Various emulsifiers, including anionic, cationic, and nonionic types, can be used as emulsifiers, and are used in an amount ranging from 0.5 to 20 parts by weight per 100 parts by weight of monomer. It is preferable to use anionic and / or nonionic and / or cationic emulsifiers. If the monomers are not completely miscible, it is preferable to add a compatibilizer that allows them to be sufficiently miscible, such as a water-soluble organic solvent or a low molecular weight monomer. Adding a compatibilizer can improve emulsification and copolymerization properties. 【0218】 The oil-resistant composition may be in the form of a solution, emulsion (especially an aqueous dispersion), or aerosol. 【0219】 <Pulp Composition> The pulp composition in this disclosure comprises an oil-resistant composition and a pulp base material. The pulp composition in this disclosure may exhibit excellent oil resistance and / or water resistance, preferably both. 【0220】The pulp composition in this disclosure is obtained by adding an oil-resistant composition to a pulp substrate. The pulp composition may also be obtained by treating the pulp substrate with an oil-resistant composition, where the amount of oil-resistant composition added and the composition of the oil-resistant composition may be adjusted so that each component is in a desired amount. Each component that may be included in the oil-resistant composition may also be added to the pulp composition separately as an additive. 【0221】 The pulp composition in this disclosure does not necessarily have to contain any of the compounds selected from the group consisting of compounds having 8 or more carbon atoms in a fluoroalkyl group, compounds having 8 or more carbon atoms in a perfluoroalkyl group, compounds having 4 or more carbon atoms in a fluoroalkyl group, compounds having 4 or more carbon atoms in a perfluoroalkyl group, compounds having a perfluoroalkyl group, compounds having a fluoroalkyl group, and compounds having a fluorine atom. The pulp composition in this disclosure can impart liquid repellency to a substrate even without containing these fluorine compounds. 【0222】 The pH of the pulp composition may be 3 to 10, for example 5 to 9, and particularly 6 to 8, and the amounts of each component may be adjusted to achieve such a pH. 【0223】 [Pulp-based material] The pulp composition includes a pulp-based material. The pulp-based material is composed of pulp, which may be wood pulp, non-wood pulp, recycled paper pulp, etc., and may include at least bagasse pulp. 【0224】[Wood Pulp] Wood pulp includes coniferous kraft pulp obtained from genera such as fir and pine, and hardwood kraft pulp obtained from genera such as acacia, eucalyptus, beech, and aspen (for example, poplar). Examples of coniferous kraft pulp include unbleached coniferous kraft pulp (NUKP), bleached coniferous kraft pulp (NBKP), semi-bleached coniferous kraft pulp (NSBKP), and sulfite coniferous pulp. Examples of hardwood kraft pulp include unbleached hardwood kraft pulp (LUKP), bleached hardwood kraft pulp (LBKP), semi-bleached hardwood kraft pulp (LSBKP), and sulfite hardwood pulp. The pulp used may be used alone or in combination. In addition to kraft pulp, there are also softwood kraft pulp and hardwood kraft pulp, as well as mechanical pulps such as stone ground pulp (SGP), pressure stone ground pulp (PGW), refiner ground pulp (RGP), thermo ground pulp (TGP), chemiground pulp (CGP), crushed wood pulp (GP), and thermomechanical pulp (TMP). Furthermore, recycled paper pulp includes disintegrated recycled paper pulp, disintegrated and deinked recycled paper pulp, or disintegrated, deinked and bleached recycled paper pulp, which are produced from brown recycled paper, recycled kraft envelopes, recycled magazines, recycled newspapers, recycled flyers, recycled office paper, recycled cardboard, recycled white recycled paper, recycled Kent paper, recycled imitation paper, recycled land deed paper, etc. 【0225】 [Non-wood pulp] Examples of non-wood pulp include bagasse, kenaf, bamboo, linter, cotton, linen, hemp, ramie, straw, esparto, Manila hemp, sisal hemp, jute, flax, ganpi, mitsumata, and kō. 【0226】 [Synthetic Fibers] The pulp composition may contain synthetic fibers. Examples of synthetic fibers that can be used include polyester fibers such as polyamide fibers and polyethylene terephthalate fibers (hereinafter also referred to as PET or PET fibers), polyolefin fibers such as acrylic fibers, polyethylene fibers, and polypropylene fibers, aramid fibers, polyethylene naphthalate fibers, polybutylene terephthalate fibers, polyphenylene sulfide fibers (hereinafter also referred to as PPS fibers), polyacetal fibers, liquid crystal polymer fibers, glass fibers, and polyimide fibers. Pulp obtained from these materials is also an example. 【0227】 [Pulp Fiber Length] From the viewpoint of improving oil resistance, the average fiber length of the pulp is preferably 0.1 mm or more, more preferably 0.3 mm or more, and even more preferably 0.5 mm or more. From the viewpoint of ease of manufacture, it is preferably 5.0 mm or less, more preferably 4.0 mm or less, even more preferably 3.0 mm or less, particularly preferably 2.0 mm or less, and most preferably 1.2 mm or less. 【0228】 [Pulp fiber width] From the viewpoint of improving oil resistance, the average fiber diameter of the pulp is preferably 5 μm or more, more preferably 10 μm or more, even more preferably 15 μm or more, and also preferably 50 μm or less, more preferably 40 μm or less, and even more preferably 30 μm or less. 【0229】 [Composition of pulp base material] When bagasse pulp is used, the pulp base material may contain more than 0% by weight, 10% or more by weight, 20% or more by weight, 30% or more by weight, 40% or more by weight, 50% or more by weight, 60% or more by weight, or 70% or more by weight, preferably 20% or more by weight, and may also contain 100% or less by weight, 90% or less by weight, 80% or less by weight, 70% or less by weight, 60% or less by weight, 50% or less by weight, 40% or less by weight, 30% or less by weight, 20% or less by weight, or 10% or less by weight, for example, 80% or less by weight. 【0230】 The total amount of pulp other than bagasse may be 0% by weight or more, 10% by weight or more, 20% by weight or more, 30% by weight or more, 40% by weight or more, 50% by weight or more, 60% by weight or more, or 70% by weight or more in the pulp base material, and may also be 99% by weight or less, 90% by weight or less, 80% by weight or less, 70% by weight or less, 60% by weight or less, 50% by weight or less, 40% by weight or less, 30% by weight or less, 20% by weight or less, or 10% by weight or less. 【0231】The amount of wood pulp may be 0% by weight or more, 10% by weight or more, 20% by weight or more, 30% by weight or more, 40% by weight or more, 50% by weight or more, 60% by weight or more, or 70% by weight or more in the pulp base material, and may also be 99% by weight or less, 90% by weight or less, 80% by weight or less, 70% by weight or less, 60% by weight or less, 50% by weight or less, 40% by weight or less, 30% by weight or less, 20% by weight or less, or 10% by weight or less. 【0232】 [Form of pulp base material] The form of the pulp base material when the oil-resistant composition is added may be pulp alone, pulp slurry, pulp products, etc. Specific examples include bleached or unbleached chemical pulp such as kraft pulp or sulfite pulp, bleached or unbleached high-yield pulp such as wood pulp, mechanical pulp or thermomechanical pulp; pulp slurry containing the pulp; and pulp products such as paper, paper containers, and pulp molded articles. 【0233】 The amount of pulp base material may be 0.1% by weight or more, 0.5% by weight or more, 1% by weight or more, 3% by weight or more, 5% by weight or more, 10% by weight or more, 20% by weight or more, 30% by weight or more, 50% by weight or more, 75% by weight or more, or 90% by weight or more in the pulp composition, and may also be 99% by weight or less, 75% by weight or less, 50% by weight or less, 40% by weight or less, 30% by weight or less, 20% by weight or less, 10% by weight or less, 5% by weight or less, 4% by weight or less, or 3% by weight or less. Typically, when the pulp composition is prepared by internal additives, the amount of pulp base material is 30% by weight or less in the pulp composition, and when the pulp composition is prepared by external additives, the amount of pulp base material may be 75% by weight or more in the pulp composition. 【0234】 The amount of pulp base material may be 50% by weight or more, 60% by weight or more, 70% by weight or more, 80% by weight or more, 90% by weight or more, 95% by weight or more, or 99% by weight or more in the pulp composition excluding the liquid medium, and may also be 99.9% by weight or less, 95% by weight or less, 90% by weight or less, 85% by weight or less, 75% by weight or less, 65% by weight or less, or 55% by weight or less. 【0235】[Liquid Media] The pulp composition may contain a liquid media. The liquid media may be water, an organic solvent, or a mixture of water and an organic solvent, and is typically an aqueous media, particularly water. The liquid media may also contain a liquid media derived from the oil-resistant composition. 【0236】 [Amount of liquid medium] The amount of liquid medium may be 0.1% by weight or more, 0.5% by weight or more, 1% by weight or more, 3% by weight or more, 5% by weight or more, 10% by weight or more, 20% by weight or more, 30% by weight or more, 50% by weight or more, 75% by weight or more, 90% by weight or more, or 95% by weight or more in the pulp composition, and may also be 99% by weight or less, 75% by weight or less, 50% by weight or less, 40% by weight or less, 30% by weight or less, 20% by weight or less, 10% by weight or less, 5% by weight or less, 4% by weight or less, or 3% by weight or less. Typically, when the pulp composition is prepared by internal additives, the amount of liquid medium is 50% by weight or more, particularly 90% by weight or more in the pulp composition, and when the pulp composition is prepared by external additives, the amount of liquid medium is 30% by weight or less, particularly 10% by weight or less in the pulp composition. 【0237】 [Oil-resistant composition] This composition includes a pulp composition and an oil-resistant composition. For details of the oil-resistant composition, refer to the description of the oil-resistant composition in <Oil-resistant composition>. 【0238】 [Amount of oil-resistant composition] The amount of oil-resistant composition may be 0.1% by weight or more, 0.3% by weight or more, 0.5% by weight or more, 0.75% by weight or more, 1.0% by weight or more, 2.0% by weight or more, or 3.0% by weight or more, relative to the pulp substrate, preferably 0.5% by weight or more, and may also be 25% by weight or less, 20% by weight or less, 15% by weight or less, 10% by weight or less, 7.5% by weight or less, 5.0% by weight or less, 4.0% by weight or less, 3.0% by weight or less, 2.0% by weight or less, 1.0% by weight or less, 0.75% by weight or less, or 0.5% by weight or less, for example 15% by weight or less, 5.0% by weight or less, or 3.0% by weight or less. 【0239】 The oil-resistant composition may be applied as an external additive to the surface of a pulp substrate (e.g., pulp products such as paper, paper containers, and pulp molded articles), and the amount of the oil-resistant composition contained in the coating layer formed by the external additive treatment is 0.01 g / m². ２Above, 0.03g / m ２ Above, 0.05g / m ２ Above, 0.1g / m ２ Above, 0.3g / m ２ Above, 0.5g / m ２ Above, or 1.0 g / m ２ The above is sufficient, and also 5.0 g / m ２ Below, 4.0g / m ２ Below, 3.0g / m ２ Below, 2.0g / m ２ Below, 1.0g / m ２ Below, 0.5g / m ２ Below, 0.3g / m ２ The following, or 0.1 g / m ２ The following is acceptable: 【0240】 [Dispersant] The pulp composition may contain a dispersant. For details on the types of dispersants, refer to the explanation of dispersants in <Oil-resistant Compositions>. 【0241】 [Amount of dispersant] The amount of dispersant may be 0.001% by weight or more, 0.01% by weight or more, 0.1% by weight or more, 0.3% by weight or more, 0.5% by weight or more, 0.75% by weight or more, 1.0% by weight or more, 2.0% by weight or more, or 3.0% by weight or more relative to the pulp substrate, and may also be 10% by weight or less, 7.5% by weight or less, 5.0% by weight or less, 4.0% by weight or less, 3.0% by weight or less, 2.0% by weight or less, 1.0% by weight or less, 0.75% by weight or less, or 0.5% by weight or less, preferably 5.0% by weight or less, more preferably 3.0% by weight or less. 【0242】[Paper Strengthening Agents] Pulp compositions may contain paper strengthening agents. Examples of paper strengthening agents include: polyacrylamide-based paper strengthening agents such as cationic polyacrylamide, anionic polyacrylamide, and amphoteric polyacrylamide; starch, enzyme-modified starch, thermochemically modified starch, oxidized starch, esterified starch, etherified starch (e.g., hydroxyethylated starch), aldehyde starch, cationic starch, starch, xanthan gum, karaya gum, welan gum, guar gum, pectin, tamarind gum, carrageenan, chitosan, gum arabic, locust bean gum, cellulose, alginic acid, agar, dextran, cellulose, carboxymethylcellulose, hydroxyethylcellulose, hydroxypropylcellulose, chitin nanofibers, cellulose nanofibers, cellulose nanocrystals, and pullulan, and polysaccharide-based paper strengthening agents such as modified polysaccharides (e.g., modified polysaccharides into which hydroxyl groups or cationic groups have been introduced); Examples of paper strength agents include polyamide resins, polyamine resins, polyamide-polyamine resins, polyamide-epichlorohydrin resins, polyamide-polyamine-epichlorohydrin resins, polyamide-polyurea-formaldehyde resins, and epoxidized polyamide resins; urea / melamine-based paper strength agents such as urea resins, melamine resins, urea-formaldehyde resins, and melamine-formaldehyde resins; polyvinyl alcohol-based paper strength agents such as polyvinyl alcohol, fully saponified polyvinyl alcohol, partially saponified polyvinyl alcohol, ethylene-modified polyvinyl alcohol, carboxyl-modified polyvinyl alcohol, silanol-modified polyvinyl alcohol, acetoacetyl-modified polyvinyl alcohol, cation-modified polyvinyl alcohol, diacetone-modified polyvinyl alcohol, and terminal alkyl-modified polyvinyl alcohol; and styrene-butadiene copolymers, polyvinyl acetate, vinyl chloride-vinyl acetate copolymers, polyvinyl chloride, polyvinylidene chloride, polyacrylic acid esters, fatty acid diamides, polyethyleneimine resins, and ketone aldehyde resins. In this disclosure, polyacrylamide-based paper strength agents, polysaccharide-based paper strength agents, or polyamide-based paper strength agents are preferred. 【0243】[Amount of paper strength agent] The amount of paper strength agent may be 0.1% by weight or more, 0.3% by weight or more, 0.5% by weight or more, 0.75% by weight or more, 1.0% by weight or more, 2.0% by weight or more, or 3.0% by weight or more relative to the pulp, and may also be 10% by weight or less, 7.5% by weight or less, 5.0% by weight or less, 4.0% by weight or less, 3.0% by weight or less, 2.0% by weight or less, 1.0% by weight or less, 0.75% by weight or less, or 0.5% by weight or less, preferably 5.0% by weight or less. 【0244】 [Sizing agents] The pulp composition may contain sizing agents. Examples of sizing agents include cationic sizing agents, anionic sizing agents, neutral sizing agents, and amphoteric sizing agents, such as rosin-based sizing agents (e.g., acidic rosin-based sizing agents, neutral rosin-based sizing agents), alkyl ketene dimers, and alkenyl succinic anhydride. 【0245】 [Amount of sizing agent] The amount of sizing agent may be 0.1% by weight or more, 0.2% by weight or more, 0.3% by weight or more, 0.5% by weight or more, 0.75% by weight or more, 1.0% by weight or more, 2.0% by weight or more, or 3.0% by weight or more relative to the pulp, and may also be 10% by weight or less, 7.5% by weight or less, 5.0% by weight or less, 4.0% by weight or less, 3.0% by weight or less, 2.0% by weight or less, 1.0% by weight or less, 0.75% by weight or less, or 0.5% by weight or less. 【0246】 [Binder] The pulp composition may contain a binder such as a water-soluble polymer like casein, or a polyester resin, polyurethane resin, styrene-butadiene resin, vinyl acetate resin, ethylene-vinyl acetate resin, acrylonitrile-butadiene resin, polyethylene resin, polypropylene resin, carboxymethylcellulose resin, polyamide resin, vinyl chloride resin, or vinylidene chloride resin. 【0247】[Pigments] The pulp composition may also contain inorganic pigments such as kaolin, light calcium carbonate, heavy calcium carbonate, magnesium carbonate, magnesium oxide, aluminum hydroxide, alumina, silica, magnesium aluminosilicate, calcium silicate, white carbon, bentonite, zeolite, sericite, smectite, calcium sulfate, barium sulfate, synthetic mica, titanium dioxide, and zinc oxide; as well as polydienes such as polyisoprene, polyneoprene, and polybutadiene; polyalkenes such as polybutene, polyisobutylene, and polypropylene; polymers and copolymers of vinyl monomers such as vinyl acetate, styrene, (meth)acrylic acid, alkyl (meth)acrylate, (meth)acrylamide, and methyl vinyl ether; and organic pigments such as various dense, hollow, or through-pore particles of polyurethane resins, polyester resins, polyamide resins, urea resins, melamine resins, and benzoguanamine resins. 【0248】 [Other Additives] In addition to the above, the pulp composition may also contain other additives such as fixing agents (aluminum sulfate, etc.), coagulants / flocculants (polyamine resins, etc.), yield improvers (polyacrylamide resins, etc.), organic acids (formic acid, acetic acid, etc.), dyes, slime control agents, defoamers, polycarboxylic acids, waxes, and penetrants, which are paper-use chemicals used in the manufacture of pulp products. 【0249】 [Amount of other additives] The amount of other additives may be 0.01% by weight or more, 0.1% by weight or more, 1% by weight or more, 3% by weight or more, 5% by weight or more, based on the pulp base material, or 30% by weight or less, 20% by weight or less, 10% by weight or less, 5% by weight or less, 3% by weight or less, or 1% by weight or less. 【0250】 <Method for producing pulp composition / pulp product> The pulp composition in this disclosure can be obtained by treating a pulp substrate with an oil-resistant composition. 【0251】 The obtained pulp composition can be subjected to processing steps such as drying, heating, and molding as necessary to obtain a pulp product to which the hydrocarbon polymer-containing polymer and crosslinking agent component of this disclosure are attached. 【0252】 The oil-resistant composition in this disclosure can be applied to pulp substrates as a treatment agent (particularly a surface treatment agent) by conventionally known methods. The treatment method may involve diluting the oil-resistant composition in an organic solvent or water as needed, and then applying it to the interior and / or surface of the pulp substrate by known methods such as immersion coating, spray coating, or foam coating, followed by drying. The dilution ratio may be appropriately changed depending on the concentration and application of the oil-resistant composition, but may be 3 to 2000 times, for example, 10 to 100 times. After drying, a pulp product with the solid components of the oil-resistant composition attached is obtained. Furthermore, if necessary, it may be applied together with a suitable crosslinking agent and curing may be performed. 【0253】 The oil-resistant composition can be applied to the pulp substrate by any known method for treating the pulp substrate with a liquid. The pulp substrate may be immersed in the oil-resistant composition, the pulp substrate and the oil-resistant composition may be mixed, or the solution may be applied to or sprayed onto the pulp substrate. The treated pulp substrate is preferably dried and cured by heating to develop liquid repellency. The heating temperature may be, for example, 100°C to 200°C, 100°C to 170°C, or 100°C to 120°C. In this disclosure, the heating time may be 5 seconds to 60 minutes, for example, 30 seconds to 3 minutes. 【0254】As a method for processing pulp substrates, an internal processing method in which an oil-resistant composition is added to the pulp substrate before papermaking (e.g., in the form of a pulp slurry) or an external processing method in which an oil-resistant composition is applied to the pulp substrate after papermaking (e.g., a pulp product) can be used. Examples of internal processing methods include mixing and immersion, and may include a step of adding the oil-resistant composition to the pulp slurry and stirring and mixing it. Examples of external processing methods include spraying, coating, immersion, and foam coating, and specifically include a pound-type two-roll size press, a gate-roll type, and a rod-metering size press. The processing may be either external or internal. For example, when the pulp substrate is paper, the paper may be coated, or the solution may be attached to or sprayed onto the paper, or it may be mixed with the pulp slurry before papermaking. When the pulp substrate is a fibrous material, examples of processing methods include padding, immersion, spraying, and coating. For padding treatment, for example, methods using padding equipment described on pages 396-397 of the Dictionary of Textile Dyeing and Processing (published in 1963 by Nikkan Kogyo Shimbun) and pages 256-260 of Color Dyeing Chemistry III (published in 1975 by Jikkyo Shuppan Co., Ltd.) can be used. For coating treatment, for example, methods using coating machines described on pages 473-477 of the General Catalog of Dyeing and Finishing Equipment (published in 1981 by Senryo-sha) can be used. For immersion treatment, for example, methods using batch-type dyeing machines described on pages 196-247 of the General Catalog of Dyeing and Finishing Equipment (published in 1981 by Senryo-sha) can be used, and liquid flow dyeing machines, air flow dyeing machines, drum dyeing machines, winch dyeing machines, washer dyeing machines, cheese dyeing machines, etc. can be used. For spray treatment, for example, methods using air sprays that atomize the treatment liquid with compressed air and spray it, or air sprays using a liquid pressure atomization method can be used. 【0255】The processing method may be an internal additive treatment in which an oil-resistant composition is added to the pulp slurry before papermaking. The internal additive treatment may include, but is not limited to, one or more of the following steps: adding the oil-resistant composition to the pulp slurry and stirring and mixing it; dewatering the pulp composition prepared in the first step by suction through a mesh-like body of a predetermined shape to deposit the pulp composition and form a pulp molded intermediate; and molding and drying the pulp molded intermediate using a heated mold to obtain a pulp molded product. After simple drying at room temperature or high temperature, the processed paper may optionally be heat-treated depending on the properties of the paper. The heat treatment temperature may be 150°C or higher, 180°C or higher, or 210°C or higher, and may be 300°C or lower, 250°C or lower, or 200°C or lower, and may particularly be between 80°C and 180°C. By performing heat treatment in such a temperature range, excellent oil resistance and water resistance can be obtained. The pulp substrate, which has undergone internal additive treatment, may be subjected to external additive treatment with an oil-resistant composition, and further oil-resistant compositions may be applied to the surface. 【0256】 The processing method may be an external additive treatment in which an oil-resistant composition is applied to the pulp substrate after papermaking. The sizing press for external additive treatment can also be classified as follows according to the application method. One application method is the so-called pound-type two-roll sizing press, in which a coating liquid (sizing liquid) is supplied to the nip portion formed by passing paper between two rubber rolls, creating a coating liquid reservoir called a pound, and the sizing liquid is applied to both sides of the paper by passing the paper through this reservoir. Other application methods are the gate-roll type and the rod-metering sizing press, in which the sizing liquid is applied by a surface transfer type. In the pound-type two-roll sizing press, the sizing liquid easily penetrates into the interior of the paper, while in the surface transfer type, the sizing liquid components tend to remain on the surface of the paper. Compared to the pound-type two-roll sizing press, the surface transfer type allows the coating layer to remain on the surface of the paper more easily, and the coating layer formed on the surface is greater than that of the pound-type two-roll sizing press. In this disclosure, performance can be imparted to the paper even when the former pound-type two-roll sizing press is used. Paper processed in this manner can exhibit excellent oil and water resistance after simple drying at room temperature or high temperature, and optionally, depending on the properties of the paper, undergo heat treatment up to 300°C, for example, up to 200°C, and particularly within a temperature range of 80°C to 180°C. 【0257】 The paper is preferably a pulp molded product. Pulp molded products can be manufactured by a manufacturing method that includes preparing a blended pulp slurry by adding an oil-resistant composition to a slurry in which pulp is dispersed in an aqueous medium, forming a pulp molded intermediate, dewatering it, and then drying it to obtain a pulp molded product. 【0258】 To the pulp (slurry), hydrocarbon group-containing polymers and amphoteric polyacrylamide polymers, preferably hydrocarbon group-containing polymers, amphoteric polyacrylamide polymers, and anionic polyacrylamide polymers, may be added all simultaneously, two types simultaneously, or all separately, preferably in this order. For example, to the pulp (slurry), a hydrocarbon group-containing polymer may be added first, followed by the addition of amphoteric polyacrylamide polymers and anionic polyacrylamide polymers simultaneously or separately, preferably in this order. Adding the hydrocarbon group-containing polymer first is preferable because it allows for efficient fixation of hydrocarbon groups to the pulp, which can lead to better effects of the present disclosure. The content ratio (overall standard) of each component in the compounded pulp slurry can be appropriately selected according to the desired physical properties of the pulp molded product, while ensuring a high degree of filtration suitable for papermaking and dewatering. For example, it may be as follows: • Aqueous medium: 89.5–99.89% by weight, e.g., 94.5–99.69% by weight • Pulp: 0.1–5% by weight, e.g., 0.3–2.5% by weight • Hydrocarbon group-containing polymer (oil-resistant composition): 0.00001–1% by weight, e.g., 0.0001–0.5% by weight • Amphoteric polyacrylamide polymer: 0.00001–1% by weight, e.g., 0.0001–0.5% by weight • Anionic acrylamide polymer: 0.00001–1% by weight, e.g., 0.0001–0.5% by weight • Cationic coagulant (solids) 0 to 1% by weight, for example 0.00005 to 0.5% by weight; Water-resistant agent (solids): 0 to 1% by weight, for example 0.00005 to 0.5% by weight. In the above, if each component is in the form of a dispersion or the like, the percentage of solids contained in the compounded pulp slurry (overall standard) shall be indicated. 【0259】 From another perspective, the respective proportions of pulp and oil-resistant composition in the aqueous medium of the compounded pulp slurry can be appropriately selected to achieve a high degree of filtration suitable for papermaking and dewatering, for example, as follows: • Pulp: 0.1 to 5.58% by weight, particularly 0.3 to 2.64% by weight • Oil-resistant composition (solids): 0.001 to 2.79% by weight, particularly 0.005 to 1.05% by weight 【0260】 The electrical conductivity of the blended pulp slurry should be between 0.1 and 2000 μS / cm, 0.1 and 1000 μS / cm, 1 and 800 μS / cm, or 10 and 500 μS / cm. Within this range, high oil resistance can be obtained. The pH of the blended pulp slurry should be between 4 and 9, 5 and 8 is better, and 6 and 7 is even better. Within this range, high oil resistance can be obtained. The hardness of the water used in the blended pulp slurry should be 5000 ppm or less, 3000 ppm or less is better, 1000 ppm or less is particularly good, and 500 ppm or less is exceptionally good. Within this range, high oil resistance can be obtained. 【0261】 Next, a pulp mold intermediate is formed from the prepared pulp slurry, dehydrated, and then at least dried to obtain a pulp mold product. 【0262】 Papermaking, dehydration, and drying can be carried out according to conventionally known methods for pulp molds. 【0263】 For example, by filtering and dewatering the prepared pulp slurry using a mold of a desired shape with numerous pores (a filter may be provided if necessary), (e.g., by suction and / or reduced pressure), the aqueous medium can be at least partially removed from the prepared pulp slurry, and a pulp mold intermediate having a shape corresponding to the mold can be obtained. 【0264】 Drying may be carried out at a temperature that can effectively remove any remaining aqueous medium, for example, 90–250°C, particularly 100–200°C. The drying time is not particularly limited and can be selected so that the aqueous medium remaining in the pulp mold intermediate is substantially removed. The drying atmosphere is not particularly limited and can be simply the ambient atmosphere (air at normal pressure). 【0265】During and / or thereafter, if necessary, other conventionally known processes in the pulp mold, such as press molding (including heat pressing), may be carried out. 【0266】 As described above, pulp molded products can be manufactured. Such pulp molded products contain pulp and an oil-resistant composition, and can achieve high gas barrier properties and excellent water and oil resistance. 【0267】 The proportion of pulp, oil-resistant composition, etc., contained in pulp molded products can be considered to be substantially equal to the proportion of solids of these components used as raw materials (although aqueous media and other liquid media, if present, can usually be removed by drying and press molding, solids may remain without being removed or decomposed). 【0268】 In pulp molded products, the content ratio of each component (components that may remain in the pulp molded product) relative to the pulp (solid content) can be appropriately selected according to the desired physical properties of the pulp molded product, but may be as follows: • Hydrocarbon group-containing polymer: 0.01 to 10% by weight or 0.01 to 5% by weight, for example 0.05 to 2% by weight • Amphoteric polyacrylamide polymer: 0.01 to 10% by weight or 0.01 to 5% by weight, for example 0.05 to 2% by weight • Anionic acrylamide polymer: 0 to 5% by weight or 0.01 to 2% by weight, for example 0.05 to 1% by weight 【0269】 Pulp molded products contain an oil-resistant composition (added to pulp slurry and manufactured by the pulp molding process). Therefore, after use, the entire pulp molded product can be crushed and returned to its original raw material, making it suitable for recycling. Furthermore, such pulp molded products can utilize the inherent biodegradability of pulp, thus significantly reducing, and preferably virtually eliminating, the environmental burden. In addition, such pulp molded products retain the texture of pulp on the surface, and do not develop a glossy appearance that can be impaired, such as when the surface is laminated with a plastic film. 【0270】Such pulp molded products can be suitably used as food containers (including trays, etc.), for example, as storage containers for frozen foods and chilled foods. 【0271】 Specific examples of pulp products include paper, paper containers, pulp molded articles, food packaging materials, food containers, gypsum board base paper, coated base paper, medium-grade paper, general liners and cores, neutral pure white roll paper, neutral liners, rust-preventive liners and metal interleaving paper, kraft paper, neutral printing and writing paper, neutral coated base paper, neutral PPC paper, neutral thermal paper, neutral pressure-sensitive base paper, neutral inkjet paper, and neutral information paper. Pulp products can be used as oil-resistant or water-resistant paper. Suitable examples of pulp products include food packaging materials and food containers, and in particular, pulp molded articles for food contact applications. 【0272】 <Nonwoven Fabric Products / Method for Manufacturing Nonwoven Fabric Products> The nonwoven fabric products in this disclosure include an oil-resistant composition and a nonwoven fabric substrate. The nonwoven fabric products in this disclosure may have excellent oil resistance and / or water resistance, preferably both. 【0273】 The method for manufacturing a nonwoven fabric product in this disclosure includes a step of treating a nonwoven fabric substrate with an oil-resistant composition. 【0274】[Processing Method] The oil-resistant composition of this disclosure can be applied to a nonwoven fabric substrate as a treatment agent (particularly a surface treatment agent) by conventionally known methods. The oil-resistant composition of this disclosure may be diluted by dispersing it in an organic solvent or water as needed, and then applied to the surface of the substrate by known methods such as immersion coating, spray coating, foam coating, etc., and dried. After drying, a nonwoven fabric product with the solid components of the oil-resistant composition attached is obtained. If necessary, it may also be applied together with a suitable crosslinking agent and cured. Furthermore, the oil-resistant composition of this disclosure can be used in combination with various additives such as water-repellent and / or oil-repellent agents, anti-slip agents, antistatic agents, texture modifiers, softeners, antibacterial agents, flame retardants, paint fixatives, anti-wrinkle agents, drying rate modifiers, crosslinking agents, film-forming aids, compatibilizers, antifreeze agents, viscosity modifiers, ultraviolet absorbers, antioxidants, pH adjusters, insecticides, and defoaming agents. Examples of various additives may be the same as those described in the "other components" section of the oil-resistant composition described above. The concentration of the hydrocarbon-containing polymer (1) in the treatment agent that comes into contact with the substrate may be changed as appropriate depending on the application, but may be 0.01 to 10% by weight, for example, 0.05 to 5% by weight. 【0275】 [Nonwoven Fabric Base Material] Various examples of nonwoven fabric base materials can be given, but these include natural animal and plant fibers such as cotton, linen, wool, and silk; synthetic fibers such as polyamide, polyester, polyvinyl alcohol, polyacrylonitrile, polyvinyl chloride, and polypropylene; semi-synthetic fibers such as rayon and acetate; inorganic fibers such as glass fibers, carbon fibers, and asbestos fibers; or mixed fibers thereof. The nonwoven fabric base material may be a nonwoven fabric, a fabric base material in the form of clothing, or a fabric base material such as a carpet, or it may be a fiber, yarn, or intermediate product in a state before it is made into a fabric (for example, sliver or roving yarn). 【0276】Examples of natural fibers include cellulose fibers such as cotton, flax, and pulp, as well as chitin, chitosan, wool, and silk. Specific examples of wood pulp include mechanical pulps such as groundwood pulp (GP), pressed groundwood pulp (PGW), and thermomechanical pulp (TMP); chemical pulps such as high-yield unbleached softwood kraft pulp (HNKP; N material), bleached softwood kraft pulp (NBKP; N material, NB material), unbleached hardwood kraft pulp (LUKP; L material), and bleached hardwood kraft pulp (LBKP, L material); recycled paper pulp such as deinking pulp (DIP) and waste pulp (WP), and semi-chemical pulp (CP). Note that nonwoven fabric products are not paper products and do not need to contain pulp as a raw material. 【0277】 Examples of synthetic fibers include polyesters such as polyethylene terephthalate, polybutylene terephthalate, polytrimethylene terephthalate, and copolymerized polyester; polyolefins such as linear low-density polyethylene, low-density polyethylene, high-density polyethylene, and polypropylene; polyamides such as nylon 6, nylon 66, nylon 610, and nylon 46; acrylic fibers such as polyacrylonitrile; polyvinyl alcohol, polyurethane, and polyvinyl chloride. Examples of semi-synthetic fibers include acetate and triacetate. Examples of regenerated fibers include rayon, cupro, polynosic rayon, lyocell, and Tencel. Examples of inorganic fibers include glass fiber and carbon fiber. 【0278】 "Treatment" means applying the oil-resistant composition to the substrate by immersion, spraying, coating, etc. Through treatment, the polymer, which is the active ingredient of the oil-resistant composition, penetrates into the substrate and / or adheres to the surface of the substrate. 【0279】The oil-resistant composition can be applied to a nonwoven fabric substrate (e.g., cloth) by any known method for treating the nonwoven fabric substrate with a liquid. The nonwoven fabric substrate may be immersed in the oil-resistant composition, or the solution may be applied to or sprayed onto the nonwoven fabric substrate. The treated substrate is preferably dried and cured by heating to exhibit water- and oil-repellent properties. The heating temperature may be, for example, 100°C to 200°C, 100°C to 170°C, or 100°C to 120°C. Good performance can also be obtained with low-temperature heating (e.g., 100°C to 140°C) in this disclosure. The heating time may be 5 seconds to 60 minutes in this disclosure, for example, 30 seconds to 3 minutes. 【0280】 Alternatively, the oil-resistant composition may be applied to the nonwoven fabric substrate by a cleaning method, for example, by washing or dry cleaning. 【0281】 [Pretreatment of nonwoven fabric substrate] The nonwoven fabric substrate may be pretreated before being treated with the oil-resistant composition of this disclosure. Pretreatment of the nonwoven fabric substrate can impart excellent durability to the nonwoven fabric product after treatment with the oil-resistant composition. 【0282】 Examples of pretreatments for nonwoven fabric substrates include cationization by reaction with reactive quaternary ammonium salts, anionization by sulfonation, carboxylation, phosphorylation, etc., acetylation, benzoylation, carboxymethylation, grafting, tannic acid treatment, and polymer coating after anionization. 【0283】 The method for pre-treating the nonwoven fabric substrate is not limited, but it can be pre-treated by conventionally known methods. The pre-treatment solution may be diluted by dispersing it in an organic solvent or water as needed, and then applied to the surface of the nonwoven fabric substrate by known methods such as immersion coating, spray coating, or foam coating, followed by drying. The pH and temperature of the pre-treatment solution may be adjusted according to the desired degree of treatment. 【0284】 The pretreatment method for nonwoven fabric substrates involves adding -SO to the fibers. ３ M １ (In the formula, M １(represents a monovalent cation) a monovalent group represented by -COOM ２ (In the formula, M ２ A monovalent group represented by (where represents a monovalent cation), and -O-P(O)(OX １ ) (OX ２ ) (wherein, X １ and X ２ The process may include a step of conferring at least one functional group (hereinafter sometimes referred to as a "specific functional group") selected from the group consisting of monovalent groups (each independently representing a hydrogen atom or an alkyl group having 1 to 22 carbon atoms). 【0285】 M １ Examples include H, K, Na, or ammonium ions which may have substituents. ２ Examples include H, K, Na, or ammonium ions which may have substituents. １ or X ２ If it is an alkyl group, it is preferably an alkyl group having 1 to 22 carbon atoms, and more preferably an alkyl group having 4 to 12 carbon atoms. 【0286】 Fibers containing the above-mentioned specific functional groups (hereinafter sometimes referred to as "functional group-containing fibers") can be prepared, for example, by the following methods: (i) A compound having the above-mentioned specific functional group is attached to a fiber material. Note that the attachment of the compound may be such that a portion of the compound and a portion of the fiber are chemically bonded, to the extent that a sufficient amount of the above-mentioned specific functional group remains. (ii) Fibers are prepared in which the above-mentioned specific functional group is directly introduced into the material constituting the fiber. 【0287】 (i) For example, a functional group-containing fiber can be obtained by a functional group introduction step in which the fiber material is treated with a pretreatment solution containing one or more compounds having the above-mentioned specific functional group. 【0288】There are no particular restrictions on the material of the fiber material, and examples include natural fibers such as cotton, linen, silk, and wool; semi-synthetic fibers such as rayon and acetate; synthetic fibers such as polyamide (nylon, etc.), polyester, polyurethane, and polypropylene; and composite fibers and blended fibers thereof. The fiber material may take any form, such as fibers (tow, sliver, etc.), yarn, knitted fabrics (including interwoven fabrics), woven fabrics (including interwoven fabrics), nonwoven fabrics, and paper. 【0289】 In this embodiment, from the viewpoint of obtaining good water repellency in the resulting nonwoven fabric product, it is preferable to use fiber materials containing polyamide and polyester as materials, and in particular, it is preferable to use nylon such as nylon 6, nylon 6,6, polyester such as polyethylene terephthalate (PET), polytrimethyl terephthalate, polylactic acid, and mixed fibers containing these. 【0290】 Above - SO ３ M １ As a compound having this property, phenolic polymers can be used. Examples of such phenolic polymers include those containing at least one compound represented by the following general formula. 【0291】 [In formula (2), X ２ Ha-SO ３ M ３ (In the formula, M ３ (where represents a monovalent cation) or a group represented by the following general formula, where n is an integer between 20 and 3000. 【0292】 [In the formula, M ４ This represents a monovalent cation. 【0293】 The above M ３ Examples include H, K, Na, or ammonium ions which may have substituents. 【0294】 The above M ４ Examples include H, K, Na, or ammonium ions which may have substituents. 【0295】The compound represented by the above general formula may, for example, be a formalin condensate of phenolsulfonic acid or a formalin condensate of sulfonated bisphenol S. 【0296】 Above - COOM ２ Examples of compounds having this property include polycarboxylic acid polymers. 【0297】 As polycarboxylic acid polymers, for example, polymers synthesized by conventionally known radical polymerization methods using acrylic acid, methacrylic acid, maleic acid, etc. as monomers, or commercially available polymers can be used. 【0298】 One method for producing polycarboxylic acid polymers is to add a radical polymerization initiator to an aqueous solution of the monomer and / or its salt, and heat the reaction at 30 to 150°C for 2 to 5 hours. At this time, alcohols such as methanol, ethanol, isopropyl alcohol, or aqueous solvents such as acetone may be added to the aqueous solution of the monomer and / or its salt. Examples of radical polymerization initiators include persulfates such as potassium persulfate, sodium persulfate, and ammonium persulfate, redox polymerization initiators formed by combinations of persulfates and sodium bisulfite, hydrogen peroxide, and water-soluble azo polymerization initiators. These radical polymerization initiators may be used alone or in combination of two or more. Furthermore, during radical polymerization, a chain transfer agent (e.g., octyl thioglycolate) may be added to adjust the degree of polymerization. 【0299】In radical polymerization, copolymerizable monomers can be used in addition to the monomers mentioned above. Examples of copolymerizable monomers include vinyl monomers such as ethylene, vinyl chloride, and vinyl acetate, as well as acrylamide, acrylates, and methacrylates. Acrylates and methacrylates are preferably those having a hydrocarbon group with 1 to 3 carbon atoms, which may have substituents such as hydroxyl groups. Examples of such acrylates or methacrylates include methyl acrylate, methyl methacrylate, ethyl acrylate, ethyl methacrylate, 2-hydroxyethyl acrylate, 2-hydroxyethyl methacrylate, propyl acrylate, and propyl methacrylate. These copolymerizable monomers may be used individually or in combination of two or more. 【0300】 The carboxyl groups in the polycarboxylic acid polymer may be free or neutralized by alkali metals or amine compounds. Examples of alkali metals include sodium, potassium, and lithium, while examples of amine compounds include ammonia, monoethanolamine, diethanolamine, and triethanolamine. 【0301】 The weight-average molecular weight of the polycarboxylic acid polymer is preferably 1,000 to 20,000, and more preferably 3,000 to 15,000, from the viewpoint of obtaining good water repellency in the resulting nonwoven fabric product. 【0302】 For polycarboxylic acid polymers, commercially available products such as "NeoCrystal 770" (manufactured by Nikka Chemical Co., Ltd., product name) and "Cellopol PC-300" (manufactured by Sanyo Chemical Industries, Ltd., product name) can be used. 【0303】 The above -O-P(O)(OX １ ) (OX ２ Examples of compounds having the following are phosphate ester compounds represented by the following general formula. [In the formula, X １ or X ２ This is synonymous with the above, X ３ This represents an alkyl group having 1 to 22 carbon atoms. 【0304】As the phosphate ester compound mentioned above, phosphate monoesters, diesters, and triesters in which the alkyl ester portion has an alkyl group having 1 to 22 carbon atoms, as well as mixtures thereof, can be used. 【0305】 From the viewpoint of obtaining a nonwoven fabric product with good water repellency, it is preferable to use lauryl phosphate ester or decyl phosphate ester. 【0306】 For the phosphate ester compound, commercially available products such as "Phosphanol ML-200" (manufactured by Toho Chemical Industry Co., Ltd., trade name) can be used. 【0307】 The pretreatment solution containing one or more compounds having the above-mentioned specific functional groups can, for example, be an aqueous solution of the compounds described above. The pretreatment solution may also contain acids, alkalis, surfactants, chelating agents, etc. 【0308】Methods for treating fibrous materials with the above-mentioned pretreatment solution include, for example, padding, immersion, spraying, and coating. For padding, for example, methods using padding equipment described on pages 396-397 of the Dictionary of Textile Dyeing and Processing (published in 1963 by Nikkan Kogyo Shimbun) and pages 256-260 of Color Dyeing Chemistry III (published in 1975 by Jikkyo Shuppan Co., Ltd.) can be used. For coating, for example, methods using coating machines described on pages 473-477 of the General Catalog of Dyeing and Finishing Equipment (published in 1981 by Senshi-sha) can be used. For immersion, for example, methods using batch-type dyeing machines described on pages 196-247 of the General Catalog of Dyeing and Finishing Equipment (published in 1981 by Senshi-sha) can be used, and liquid flow dyeing machines, air flow dyeing machines, drum dyeing machines, winch dyeing machines, washer dyeing machines, cheese dyeing machines, etc. can be used. Examples of spray treatments include air sprays that atomize the treatment solution using compressed air, and air sprays that use a hydraulic atomization system. The concentration of the treatment solution and the treatment conditions such as heat treatment after application can be adjusted as appropriate, taking into consideration the purpose, performance, and other conditions. If the pretreatment solution contains water, it is preferable to dry it to remove the water after it has been applied to the fiber material. There are no particular restrictions on the drying method, and either a dry heat method or a wet heat method may be used. There are no particular restrictions on the drying temperature, but for example, drying at room temperature to 200°C for 10 seconds to several days is sufficient. If necessary, after drying, heat treatment may be performed at a temperature of 100 to 180°C for about 10 seconds to 5 minutes. 【0309】 Furthermore, if the fiber material is to be dyed, the pretreatment with the pretreatment solution may be performed before dyeing or in the same bath as the dyeing. However, if reducing soaping is performed, there is a risk that the compounds having the specific functional groups adsorbed during the process (for example, phenolic polymer compounds, etc.) may be removed. Therefore, it is preferable to perform the pretreatment after reducing soaping following dyeing. 【0310】 The treatment temperature during the immersion process can be 60 to 130°C. The treatment time can be 5 to 60 minutes. 【0311】In the functional group introduction step using the pretreatment solution, it is preferable to treat the material in such an amount that the amount of compound having the specified functional group attached is 1.0 to 7.0 parts by weight per 100 parts by weight of the fiber material. Within this range, a high level of both durable water repellency and texture can be achieved. 【0312】 The pretreatment solution is preferably adjusted to a pH of 3 to 5. pH adjustment can be done using pH adjusting agents such as acetic acid or malic acid. 【0313】 In the pretreatment solution, salt can also be used in combination to effectively adsorb the compound having the above-mentioned specific functional group onto the fiber material through a salting-out effect. Examples of salts that can be used include sodium chloride, sodium carbonate, ammonium sulfate, and sodium sulfate. 【0314】 In the functional group introduction step using a pretreatment solution, it is preferable to remove any compounds having the specified functional groups that have been excessively treated. One method of removal is washing with water. By performing sufficient removal, it is possible to suppress the inhibition of the development of water repellency in the subsequent water-repellent treatment, and in addition, the texture of the resulting nonwoven fabric product will be improved. Furthermore, it is preferable to thoroughly dry the resulting functional group-containing fibers before contacting them with a hydrocarbon-based water repellent. 【0315】 (ii) Examples of fibers in which the above-mentioned specific functional groups are directly introduced into the material constituting the fiber include cationic dyeable polyester (CD-PET). 【0316】 From the viewpoint of obtaining good water repellency in the resulting textile product, the functional group-containing fibers preferably have a surface zeta potential of -100 to -0.1 mV, and more preferably -50 to -1 mV. The surface zeta potential of the fibers can be measured, for example, using the zeta potential and particle size measurement system ELSZ-1000ZS (manufactured by Otsuka Electronics Co., Ltd.). 【0317】 Although embodiments have been described above, it should be understood that various modifications to the form and details are possible without departing from the spirit and scope of the claims. 【0318】The present disclosure will be described in detail below with reference to examples, but the present disclosure is not limited to these examples. 【0319】 <Testing Method> The testing procedure is as follows: 【0320】 [KIT Test] Oil resistance (KIT method) was measured according to TAPPI T-559cm-02. The KIT test solution is a mixture of castor oil, toluene, and heptane in the ratios shown in Table 1. One drop of the test solution shown in the table below was placed on paper, and the degree of oil penetration was observed after 15 seconds. The highest oil resistance score given by the KIT test solution that did not show penetration was defined as the oil resistance. A higher KIT test solution number indicates higher oil resistance. 【0321】 【0322】 [High-Temperature Oil Resistance Test] A small amount of commercially available olive oil was dropped onto the prepared oil-resistant paper, and it was placed in a 70°C oven for 5 minutes before being removed and the oil wiped off. After that, the degree of absorption of the oil-resistant paper was visually observed and evaluated according to the following criteria: ○: No oil stains observed ○△: Scattered oil stains observed △: Oil stains observed on less than half of the oil droplet contact surface ×: Oil stains observed on more than half of the oil droplet contact surface 【0323】<Synthesis Examples> [Synthesis Example 1] A 500 ml reactor equipped with a stirrer, thermometer, reflux condenser, dropping funnel, nitrogen inlet, and heating device was prepared, and 100 parts of the solvent methyl ethyl ketone (MEK) were added. Subsequently, under stirring, monomers consisting of 78 parts of stearyl amide ethyl acrylate (C18AmEA, melting point: 70°C), 16 parts of hydroxybutyl acrylate (HBA, Tg: -40°C), and 6 parts of dimethylaminoethyl methacrylate (DM) (total monomers: 100 parts), and 1.2 parts of the initiator perbutyl PV (PV) were added in this order, and copolymerization was carried out by mixing and stirring this mixture under a nitrogen atmosphere at 65-80°C for 12 hours. The solid content concentration of the obtained copolymer-containing solution was 50% by weight. The obtained copolymer solution was added to water containing approximately 3 g of acetic acid and dispersed. Then, the solution was heated using an evaporator, and MEK was removed by distillation under reduced pressure to obtain a milky white copolymer aqueous dispersion (containing 1% by weight or less of volatile organic solvents). Deionized water was added to obtain an aqueous dispersion with a solid content of 15% by weight. The melting point of this copolymer was 70°C. 【0324】 [Synthesis Example 2] The same procedure as in Synthesis Example 1 was used, except that 75 parts of stearyl acrylate (StA, melting point: 30°C), 22 parts of hydroxybutyl acrylate (HBA, Tg: -40°C), and 3 parts of dimethylaminoethyl methacrylate (DM) were used instead of stearyl amide ethyl acrylate (C18AmEA, melting point: 70°C), to obtain a milky white copolymer aqueous dispersion (volatile organic solvent content: 1% by weight or less). Deionized water was added to obtain an aqueous dispersion with a solid content of 15% by weight. The melting point of this copolymer was 48°C. 【0325】 <Examples and Comparative Examples> [Example 1] Composed of a mixed pulp of LBKP (= bleached hardwood kraft pulp) and NBKP (bleached softwood kraft pulp), with a basis weight of 47 g / m² ２ The paper density is 0.77 g / cm³. ３ The air permeability is 200 seconds, and the Cobb value is 51 g / m². ２A paper substrate was used as the base paper. The oil resistance of this base paper showed a KIT value of 0 and a practical oil test result of 1. An aqueous dispersion of the copolymer obtained in Synthesis Example 1 was used as an oil-resistant agent, and oil-resistant paper (processed paper) was obtained by the following formulation. 【0326】 A treatment solution was prepared by mixing the aqueous dispersion of the copolymer obtained in Synthesis Example 1 with an aqueous dispersion of starch solution and glyoxal as a crosslinking agent. The pH of the treatment solution was adjusted to 3.5 to 4.2 with a certain amount of malic acid aqueous solution, and the solid content concentrations of the copolymer, starch, and crosslinking agent were adjusted to 1.4% by weight, 14% by weight, and 0.5% by weight, respectively. 【0327】 Oil-resistant paper was obtained by treating the base paper with a processing solution at approximately 50°C using a size press and then drying it in a drum dryer. The dry coating amount of the obtained oil-resistant paper and the results of the kit test of the oil-resistant paper are shown in Table 2. The results of the high-temperature oil resistance test are shown in Table 4. The starch used here was hydroxyalkylated modified starch (viscosity of 7 cp at 50°C at 10% by weight). 【0328】 [Example 2] The same treatment as in Example 1 was carried out, except that 13.5% by weight of starch and 1% by weight of glyoxal were used in the treatment solution. The dry coating amount of the obtained oil-resistant paper and the results of the kit test of the oil-resistant paper are shown in Table 2. The results of the high-temperature oil resistance test are shown in Table 4. 【0329】 [Example 3] The same treatment as in Example 1 was carried out, except that the copolymer in the treatment solution was 1.2% by weight, the starch concentration was 0% by weight, and the glyoxal was 0.2% by weight. The dry coating amount of the obtained oil-resistant paper and the results of the kit test of the oil-resistant paper are shown in Table 2. 【0330】 [Example 4] The same treatment as in Example 3 was carried out, except that 1.4% by weight of copolymer and 1.5% by weight of glyoxal were used in the treatment solution. The dry coating amount of the obtained oil-resistant paper and the results of the kit test of the oil-resistant paper are shown in Table 2. 【0331】 [Example 5] The same procedure as in Example 1 was followed, except that the copolymer in the treatment solution used was that of Synthesis Example 2. The dry coating amount of the obtained oil-resistant paper and the results of the kit test of the oil-resistant paper are shown in Table 2. 【0332】[Example 6] The same procedure as in Example 2 was followed, except that the copolymer in the treatment solution used was that from Synthesis Example 2. The dry coating amount of the obtained oil-resistant paper and the results of the kit test of the oil-resistant paper are shown in Table 2. 【0333】 [Example 7] The same procedure as in Example 3 was followed, except that the copolymer in the treatment solution used was that from Synthesis Example 2. The dry coating amount of the obtained oil-resistant paper and the results of the kit test of the oil-resistant paper are shown in Table 2. 【0334】 [Example 8] The same procedure as in Example 4 was followed, except that the copolymer in the treatment solution used was that from Synthesis Example 2. The dry coating amount of the obtained oil-resistant paper and the results of the kit test of the oil-resistant paper are shown in Table 2. 【0335】 [Example 9] The same treatment as in Example 6 was carried out, except that 7% by weight of starch was used in the treatment solution. The dry coating amount of the obtained oil-resistant paper and the results of the kit test of the oil-resistant paper are shown in Table 2. The results of the high-temperature oil resistance test are shown in Table 4. 【0336】 [Example 10] The same procedure as in Example 9 was followed, except that the copolymer in the treatment solution used was that of Synthesis Example 1. The dry coating amount of the obtained oil-resistant paper and the results of the kit test of the oil-resistant paper are shown in Table 2. The results of the high-temperature oil resistance test are shown in Table 4. 【0337】 [Example 11] The same treatment as in Example 10 was carried out, except that the copolymer in the treatment solution was 1.2% by weight and the starch concentration was 18% by weight. The dry coating amount of the obtained oil-resistant paper and the results of the kit test of the oil-resistant paper are shown in Table 2. The results of the high-temperature oil resistance test are shown in Table 4. 【0338】 [Comparative Example 1] The same treatment as in Example 1 was carried out, except that the copolymer in the treatment solution was 2.4% by weight and glyoxal was not used. The dry coating amount of the obtained oil-resistant paper and the kit test results of the oil-resistant paper are shown in Table 3. The results of the high-temperature oil resistance test are shown in Table 4. 【0339】 [Comparative Example 2] The same treatment as in Comparative Example 1 was carried out, except that 1.4% by weight of copolymer and 15% by weight of starch were used in the treatment solution. The dry coating amount of the obtained oil-resistant paper and the kit test results of the oil-resistant paper are shown in Table 3. The results of the high-temperature oil resistance test are shown in Table 4. 【0340】[Comparative Example 3] The same treatment as in Comparative Example 2 was carried out, except that starch was not used in the treatment solution. The dry coating amount of the obtained oil-resistant paper and the kit test results of the oil-resistant paper are shown in Table 3. 【0341】 [Comparative Example 4] The same treatment as in Comparative Example 3 was carried out, except that 3% by weight of copolymer was used in the treatment solution. The dry coating amount of the obtained oil-resistant paper and the kit test results of the oil-resistant paper are shown in Table 3. 【0342】 [Comparative Example 5] The same treatment as in Comparative Example 1 was carried out, except that the copolymer in the treatment solution used was that of Synthesis Example 2. The dry coating amount of the obtained oil-resistant paper and the kit test results of the oil-resistant paper are shown in Table 3. 【0343】 [Comparative Example 6] The same treatment as in Comparative Example 2 was carried out, except that the copolymer in the treatment solution used was that of Synthesis Example 2. The dry coating amount of the obtained oil-resistant paper and the kit test results of the oil-resistant paper are shown in Table 3. 【0344】 [Comparative Example 7] The same treatment as in Comparative Example 3 was carried out, except that the copolymer in the treatment solution used was that of Synthesis Example 2. The dry coating amount of the obtained oil-resistant paper and the kit test results of the oil-resistant paper are shown in Table 3. 【0345】 [Comparative Example 8] The same treatment as in Comparative Example 4 was carried out, except that the copolymer in the treatment solution used was that of Synthesis Example 2. The dry coating amount of the obtained oil-resistant paper and the kit test results of the oil-resistant paper are shown in Table 3. 【0346】 [Comparative Example 9] The same treatment as in Comparative Example 6 was carried out, except that the copolymer in the treatment solution was not used. The dry coating amount of the obtained oil-resistant paper and the kit test results of the oil-resistant paper are shown in Table 3. 【0347】 [Comparative Example 10] The same procedure as in Example 6 was performed, except that the copolymer in the treatment solution was not used. The dry coating amount of the obtained oil-resistant paper and the kit test results of the oil-resistant paper are shown in Table 3. 【0348】 [Comparative Example 11] The same treatment as in Comparative Example 6 was carried out, except that 8% by weight of starch was used in the treatment solution. The dry coating amount of the obtained oil-resistant paper and the results of the kit test of the oil-resistant paper are shown in Table 3. 【0349】[Comparative Example 12] The same treatment as in Comparative Example 11 was carried out, except that the copolymer in the treatment solution used was that of Synthesis Example 1. The dry coating amount of the obtained oil-resistant paper and the results of the kit test of the oil-resistant paper are shown in Table 3. The results of the high-temperature oil resistance test are shown in Table 4. 【0350】 [Comparative Example 13] The same treatment as in Comparative Example 12 was carried out, except that the copolymer in the treatment solution was 1.2% by weight and the starch concentration was 19% by weight. The dry coating amount of the obtained oil-resistant paper and the results of the kit test of the oil-resistant paper are shown in Table 3. The results of the high-temperature oil resistance test are shown in Table 4. 【0351】 【0352】 【0353】

Claims

1. An oil-resistant composition comprising (1) a hydrocarbon-containing polymer having long-chain hydrocarbon groups, and (2) a crosslinking agent component.

2. The oil-resistant composition according to claim 1, wherein the crosslinking agent component is at least one selected from the group consisting of aldehyde compounds, organometallic compounds, isocyanate compounds, and epoxy compounds.

3. The oil-resistant composition according to claim 2, wherein the aldehyde compound is a glyoxal compound.

4. An oil-resistant composition according to any one of claims 1 to 3, comprising a water-soluble polymer.

5. The oil-resistant composition according to claim 4, wherein the water-soluble polymer is a polyol.

6. The oil-resistant composition according to claim 4 or 5, wherein the polyol is at least one selected from the group consisting of polysaccharides and polyvinyl alcohol.

7. The oil-resistant composition according to any one of claims 1 to 6, wherein the hydrocarbon-containing polymer comprises repeating units derived from a monomer (a) having 7 to 40 hydrocarbon groups, and repeating units derived from a hydrophilic group-containing monomer (b).

8. The monomer (a) has the formula: CH2=C(−X ａ )−C(=O)−Y ａ (R ａ ) ｋ [In the formula, R ａ is independently a hydrocarbon group having 7 to 40 carbon atoms, X ａ is a hydrogen atom, a monovalent organic group or a halogen atom, and Y ａ is a divalent to tetravalent hydrocarbon group having 1 carbon atom, -C ６ H ４ -, -O-, -C(=O)-, -S(=O) ２ - or -NH- and is a group composed of at least one or more selected therefrom, and k is 1 to 3.], The oil-resistant agent composition according to claim 7.

9. The monomer (b) is of the formula: CH ２ = CX ｂ C(=O)-Y ｂ - (R ｂ O) ｎ -A ｂ [In the formula, X ｂ is a hydrogen atom or a methyl group, Y ｂ is -O- or -NH-, and R ｂ Each of these is an alkylene group having 2 to 6 carbon atoms, and A ｂ This is a hydrogen atom, an unsaturated or saturated hydrocarbon group having 1 to 22 carbon atoms, or CH ２ = CX ｂ The oil-resistant composition according to claim 7 or 8, where C(=O)- and n is an integer from 1 to 90.

10. The oil-resistant composition according to any one of claims 1 to 9, wherein the hydrocarbon-containing polymer comprises repeating units derived from an ionic group-containing monomer (c).

11. The oil-resistant composition according to any one of claims 1 to 10, wherein the amount of the crosslinking agent component (2) is 10% by weight or more and 55% by weight or less of the total amount of the hydrocarbon-containing polymer and the crosslinking agent component (2).

12. The oil-resistant composition according to any one of claims 1 to 11, wherein the (1) hydrocarbon-containing polymer comprises repeating units derived from a monomer (a) having a hydrocarbon group having 7 to 40 carbon atoms, and repeating units derived from a hydrophilic group-containing monomer (b), and the (2) crosslinking agent component is a glyoxal compound and comprises polysaccharides.

13. The oil-resistant composition according to claim 12, further comprising repeating units derived from an ionic group-containing monomer (c), wherein the amount of the (2) crosslinking agent component is 10% by weight or more and 55% by weight or less with respect to the total amount of the (1) hydrocarbon-containing polymer and the (2) crosslinking agent component, the polysaccharide is starch, and the amount of the starch is 60% by weight or more and 99% by weight or less with respect to the oil-resistant composition.

14. An oil-resistant composition according to any one of claims 1 to 13, for use in pulp products.

15. A pulp product comprising (1) a hydrocarbon-containing polymer having long-chain hydrocarbon groups, and (2) a crosslinking agent component, in an oil-resistant composition according to any one of claims 1 to 14.

16. The pulp product according to claim 15, which is oil-resistant paper or water-resistant paper.

17. The pulp product according to claim 15 or 16, which is a food packaging material or a food container.

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