Surface-modified fibers, reinforcing fibers, and molded articles using the same

Abstract

To solve the issue of insufficient adhesion strength when bonding fibers to rubber.SOLUTION: The present invention provides surface-modified fibers and reinforcing fibers that are capable of enhancing adhesion to rubber, without the use of resorcinol and formaldehyde, and a molded article using these fibers. The surface-modified fibers include fibers, and a surface-modifying layer covering at least a part of the surface of the fibers, with the solid surface zeta potential on the surface of the surface-modifying layer ranging from -20.0 to 30.0 mV.SELECTED DRAWING: None

Description

Technical Field

[0001] The present invention relates to a surface-modified fiber, a reinforcing fiber having excellent adhesion to rubber, and a molded body using the same.

Background Art

[0002] Synthetic organic fibers such as polyethylene terephthalate (PET), nylon 66, vinylon, and rayon are inexpensive, have high strength, excellent heat resistance and durability, and are lightweight. Therefore, they are used as reinforcing fibers for automobile tires and oil brake hoses. In these products, in order to fully exhibit the excellent physical properties (for example, high strength and high elastic modulus) of rubber, it is necessary to firmly bond the fiber and the rubber.

[0003] Conventionally, as a method for firmly bonding a fiber and a rubber, a method using an adhesive called RFL mainly composed of a resorcinol-formaldehyde resin and a rubber latex is widely known (Patent Documents 1 and 2). However, formaldehyde contained in RFL is suspected of being carcinogenic, and resorcinol is suspected of being an environmental hormone. Therefore, the development of alternative materials that do not use these raw materials is desired.

[0004] As an alternative material for RFL, for example, Patent Document 3 proposes a technique using an adhesive containing an adhesive compound having an unsaturated carbon bond and an epoxy group that reacts with a vulcanizing agent used for vulcanization of rubber. Further, Patent Document 4 proposes a technique in which an active functional group layer is provided by applying a blocked isocyanate compound and an epoxy compound in the first step, and an adhesive component mainly composed of latex is used in the second step.

Prior Art Documents

Patent Documents

[0005]

Patent Document 1

Patent Document 2

[0006] The method using the adhesive described in Patent Document 3 had the problem of being less practical due to significantly inferior adhesive properties compared to the conventional method using RFL. Furthermore, the treatment described in Patent Document 4 requires a step of creating an intermediate layer called a rubberized layer and requires two stages of high-temperature heat treatment, which requires a great deal of energy for the treatment and may lead to thermal degradation of the fibers and a decrease in reinforcement performance. It should be noted that Patent Document 4 only describes a technology using an adhesive component mainly composed of latex, and does not describe the use of an adhesive component mainly composed of conjugated diene rubber.

[0007] The present invention has been made in view of the above-mentioned conventional problems, and aims to provide a surface-modified fiber, a reinforcing fiber, and a molded article using the same that can improve adhesion to rubber without using resorcinol and formaldehyde. [Means for solving the problem]

[0008] As a result of diligent research to solve the aforementioned problems, the present inventors have discovered that by attaching a specific compound to the fiber and adjusting the zeta potential of the fiber surface to a specific range, the affinity between the fiber and the adhesive component is increased, and as a result, the adhesion between the fiber and rubber is improved without the use of resorcinol and formaldehyde, thus completing the present invention.

[0009] In other words, the present invention relates to the following [1] to

[14] . [1] A surface-modified fiber having a fiber and a surface-modified layer covering at least a portion of the surface of the fiber, wherein the solid surface zeta potential at the surface of the surface-modified layer is -20.0 to 30.0 mV. [2] The surface-modified fiber according to [1], wherein the fiber is one or more fibers selected from polyester fibers, polyamide fibers, polyvinyl alcohol fibers, and regenerated cellulose fibers. [3] The surface-modified fiber according to [1] or [2], wherein the surface-modified layer contains a compound having nitrogen-containing functional groups. [4] The surface-modified fiber according to any one of [1] to [3], wherein the surface-modified layer comprises a compound having a functional group derived from one or more selected from an oxazoline group, an oxazolidinone group, a carbodiimide group, a carbamide group, an amino group, and an aziridine group. [5] The surface-modified fiber according to any one of [1] to [4], wherein the amount of the surface-modified layer is 0.01 to 5.0 parts by mass per 100 parts by mass of fiber used as raw material. [6] A reinforcing fiber having a surface-modified fiber according to any of [1] to [5] above, and an adhesive layer containing a conjugated diene rubber covering at least a portion of the surface of the surface-modified fiber. [7] The reinforcing fiber according to [6], wherein the number average molecular weight (Mn) of the conjugated diene rubber is greater than 2,000 and less than or equal to 120,000. [8] The reinforcing fiber according to [6] or [7], wherein the conjugated diene rubber has monomer units in its molecule derived from one or more selected from butadiene, isoprene, and farnesene. [9] The reinforcing fiber according to any one of [6] to [8], wherein the conjugated diene rubber is a modified conjugated diene rubber having a hydrogen bonding functional group in a part of the conjugated diene rubber, and the hydrogen bonding functional group is one or more selected from a hydroxyl group, an epoxy group, an aldehyde group, an acetal of an aldehyde group, a carboxyl group, a salt of a carboxyl group, an ester of a carboxyl group, an acid anhydride of a carboxyl group, a silanol group, an ester of a silanol group, an amino group, an imidazole group, and a mercapto group.

[10] The reinforcing fiber according to any one of [6] to [9], wherein the adhesive layer further contains oil, and the vapor pressure of the oil at 20°C is 10 Pa or less.

[11] A molded article using the reinforcing fiber described in any of [6] to

[10] above.

[12] The molded article according to

[11] , further having a rubber layer.

[13] The molded body according to

[11] or

[12] , wherein the molded body is a tire, a belt, or a hose.

[14] A molded article having fibers, a surface modification layer, an adhesive layer, and a rubber layer in this order, wherein the adhesive force between the adhesive layer and the rubber layer is 70 N or more per 25.4 mm width. [Effects of the Invention]

[0010] The present invention provides surface-modified fibers, reinforcing fibers, and molded articles using the same that can improve adhesion to rubber without using resorcinol and formaldehyde. [Modes for carrying out the invention]

[0011] [Surface-modified fibers] The surface-modified fiber of the present invention comprises a fiber and a surface-modified layer covering at least a portion of the surface of the fiber, characterized in that the solid surface zeta potential at the surface of the surface-modified layer is -20.0 to 30.0 mV. According to the present invention, since the zeta potential of the solid surface is adjusted to the aforementioned range, a strong affinity is expressed between the modified conjugated diene rubber contained in the adhesive component and the fibers. As a result, the fibers, adhesive component, and rubber are firmly bonded to each other, and the adhesion between the fibers and the rubber is improved. In this invention, the "surface modification layer covering at least a portion of the surface of the fiber" may be a surface modification layer that exists on at least a portion of the surface of the fiber, for example, as a film or layer, or it may be a surface modification layer that contains a component equivalent to the surface modification layer in the raw material of the fiber, and the component of the surface modification layer exists on a portion of the surface of the fiber itself.

[0012] From the perspective of improving the affinity between the fiber and the adhesive component, and as a result, improving the adhesion between the fiber and the rubber, the solid surface zeta potential on the surface of the surface modification layer is preferably -20.0 to 20.0 mV, more preferably -15.0 to 15.0 mV, still more preferably -10.0 to 12.0 mV, even more preferably -5.0 to 10.0 mV, even more preferably -5.0 to 9.0 mV, even more preferably -5.0 to 6.0 mV, and even more preferably -5.0 to 0 mV.

[0013] <Surface modification layer> The surface modification layer in the present invention is not particularly limited as long as it is composed of a compound capable of adjusting the solid surface zeta potential within the above range. For example, it is preferably a layer containing a compound having a nitrogen-containing functional group. Specifically, it is preferably a layer containing a compound having a functional group derived from one or more selected from an oxazoline group, an oxazolidinone group, a carbodiimide group, a carbamide group, an amino group, and an aziridine group.

[0014] Examples of the compound having the functional group include an oxazolidinone group-containing compound obtained by reacting a blocked isocyanate compound and an epoxy compound, an oxazoline group-containing compound obtained by introducing an oxazoline group into the polymer main chain of an acrylic or styrene / acrylic copolymer, a carbodiimide group-containing compound (polyvalent carbodiimide) having a carbodiimide group introduced into the molecule, a carbamide group-containing compound such as a urea derivative, an amino group-containing high molecular weight substance having an amino group introduced into the molecule, an aziridine group-containing compound (2,2-bis(hydroxymethyl)butanol tris[3-(1-aziridinyl)propionate]) having an aziridine group introduced at the molecular end, etc. Among these, from the perspective of improving the adhesion between the surface-modified fiber and the rubber, an oxazolidinone group-containing compound obtained by reacting a blocked isocyanate compound and an epoxy compound is preferable, and from the perspective of reducing the environmental load, an oxazoline group-containing compound is preferable.

[0015] From the perspective of improving the adhesion to rubber, it is preferable that the surface modification layer covers the entire surface of the fiber, but substantially, it may cover at least a part of the surface of the fiber. The specific amount of the surface modification layer covering the surface of the fiber is preferably 0.01 to 5.0 parts by mass, more preferably 0.05 to 1.0 parts by mass, and still more preferably 0.1 to 0.3 parts by mass with respect to 100 parts by mass of the fiber used as the raw material.

[0016] <Fiber> There is no particular limitation on the fiber used for the surface-modified fiber of the present invention, but it can be suitably used for hydrophobic fibers made of a hydrophobic resin that could not be strongly adhered to rubber in the prior art. Since hydrophobic fibers generally do not have polar functional groups on the fiber surface, they have poor affinity with the adhesive component described later and could not be strongly adhered to rubber. However, by providing a surface modification layer on the fiber surface as in the present invention, even hydrophobic fibers can be strongly adhered to rubber. In the present invention, the "fiber" includes not only single fibers and long fibers but also forms such as non-woven fabrics, woven fabrics, knitted fabrics, felt, and sponge.

[0017] Examples of the hydrophobic fibers that can be used in the present invention include polyolefin fibers such as polyethylene and polypropylene, polyester fibers such as polyethylene terephthalate, and wholly aromatic polyester fibers. Among these, polyester fibers are preferred because of their excellent manufacturing cost, strength, heat resistance, durability, etc.

[0018] In the present invention, hydrophilic fibers may also be used. Examples of the hydrophilic synthetic fibers include synthetic fibers composed of a thermoplastic resin having hydrophilic functional groups such as hydroxy groups, carboxy groups, sulfonic acid groups, and amino groups, and / or hydrophilic bonds such as amide bonds. Specific examples of such thermoplastic resins include polyvinyl alcohol-based resins, polyamide-based resins [aliphatic polyamides such as polyamide 6, polyamide 66, polyamide 11, polyamide 12, polyamide 610, polyamide 612, and polyamide 9C (a polyamide consisting of nonanediamine and cyclohexanedicarboxylic acid); semi-aromatic polyamides synthesized from aromatic dicarboxylic acids and aliphatic diamines such as polyamide 9T (a polyamide consisting of nonanediamine and terephthalic acid); and fully aromatic polyamides synthesized from aromatic dicarboxylic acids and aromatic diamines such as poly-p-phenylene terephthalamide], and polyacrylamide-based resins. Among these, polyvinyl alcohol-based resins and polyamide-based resins are preferred. Hydrophilic synthetic fibers may be used individually or in combination of two or more types. Furthermore, these hydrophilic synthetic fibers may be subjected to further hydrophilization treatments, as described later, to enhance their hydrophilicity.

[0019] Examples of hydrophilic natural fibers include natural cellulose fibers such as wood pulp (e.g., kraft pulp), cotton pulp, and straw pulp (e.g., non-wood pulp). Examples of hydrophilic regenerated fibers include rayon, lyocell, cupro, and polynosic, which are regenerated cellulose fibers. These natural and regenerated fibers may be used individually or in combination of two or more types. Furthermore, these hydrophilic natural and regenerated fibers may be subjected to further hydrophilization treatments, as described later, to enhance their hydrophilicity.

[0020] Hydrophilic fibers only need to have a hydrophilic surface, and may include, for example, fibers whose surface has been treated to make hydrophilic, or core-sheath composite fibers in which a hydrophobic resin is used as the core and a hydrophilic resin as the sheath. For examples of hydrophilic resins that constitute the sheath, the description of hydrophilic synthetic fibers is cited. Examples of hydrophobic fibers made of hydrophobic resin include the hydrophobic fibers mentioned above.

[0021] The hydrophilization treatment is not particularly limited as long as it is a treatment that chemically or physically imparts hydrophilic functional groups to the fiber surface. For example, it can be carried out by modifying the hydrophobic fibers made of the hydrophobic resin with a compound or derivative thereof containing hydrophilic functional groups such as isocyanate groups, epoxy groups, hydroxyl groups, amino groups, ether groups, aldehyde groups, carbonyl groups, carboxyl groups, and urethane groups, or by modifying the surface by electron beam irradiation.

[0022] From the viewpoint of using hydrophilic fibers in the present invention, synthetic fibers and regenerated fibers are preferred, and among them, one or more fibers selected from polyester fibers, polyamide fibers, polyvinyl alcohol fibers, and regenerated cellulose fibers are preferred. In this invention, one type of fiber may be used alone, or two or more types may be used in combination.

[0023] <Method for manufacturing surface-modified fibers> There are no particular limitations on the method for producing the surface-modified fibers of the present invention, but they can be produced by preparing a solution of the compounds constituting the aforementioned surface-modified layer in water or an organic solvent, applying this solution to the fibers, and then drying them by heat treatment or the like. There are no particular restrictions on the method of applying the surface modifier solution to the fibers, but it is preferable to use one or more methods selected from, for example, immersion, roll coater, oiling roller, oiling guide, nozzle (spray) application, and brush application.

[0024] The heat treatment for drying the aforementioned solution is preferably carried out at a treatment temperature of 100 to 250°C for a treatment time of 0.1 seconds to 2 minutes. The heat treatment may be performed only once at a specific temperature, or it may be performed two or more times with different treatment temperatures and treatment times.

[0025] The surface modification layer may contain other components besides those mentioned above. Examples of other components include crosslinking agents, acids, bases, inorganic salts, organic salts, pigments, dyes, antioxidants, polymerization initiators, and plasticizers. If the surface modification layer contains the other components, the content of the other components in the surface modification layer is preferably 20% by mass or less, more preferably 10% by mass or less, and even more preferably 5% by mass or less, from the viewpoint of improving adhesion to rubber.

[0026] [Reinforcement fibers] The reinforcing fiber of the present invention comprises the surface-modified fiber of the present invention and an adhesive layer containing a conjugated diene rubber covering at least a portion of the surface of the surface-modified fiber. In the present invention, because of the high affinity between the surface-modified fiber and the adhesive layer, it becomes possible to firmly bond the fiber to the adhesive layer and the adhesive layer to the rubber. The reinforcing fiber of the present invention may have its entire surface covered with an adhesive layer, or at least a portion of it may be covered with an adhesive layer, for example, the adhesive component may exist as a film or layer.

[0027] Furthermore, in the present invention, reinforcing fibers with excellent adhesion to rubber can be obtained even without containing formaldehyde or formaldehyde-based resins, which are harmful to the human body. In the present invention, if the adhesive layer contains a formaldehyde-based resin, examples of such resins include resolol / formaldehyde resin, phenol / formaldehyde resin, melamine / formaldehyde resin, and derivatives thereof. If the adhesive layer contains the formaldehyde component, its content is preferably 10 parts by mass or less, more preferably 5 parts by mass or less, even more preferably 3 parts by mass or less, particularly preferably 1 part by mass or less, and particularly preferably substantially omitted, per 100 parts by mass of the conjugated diene rubber. The formaldehyde content can be measured by extracting the adhesive layer from the reinforcing fibers with a solvent such as toluene, and then using HPLC or the like.

[0028] <Adhesive layer> The adhesive layer in the reinforcing fiber of the present invention is not particularly limited as long as it contains a conjugated diene rubber. For example, it can be formed by attaching an adhesive component consisting of a solution of conjugated diene rubber dissolved in oil, or an adhesive component consisting of an emulsion of conjugated diene rubber dispersed in water, to the surface-modified fiber. The embodiments of the adhesive layer will be described in detail below.

[0029] [Conjugated diene rubber] The conjugated diene rubber used in the present invention contains at least monomer units derived from a conjugated diene (hereinafter also referred to as "conjugated diene units") within its molecule, and preferably contains 50 mol% or more of monomer units derived from a conjugated diene in the total monomer units in the conjugated diene rubber. Examples of the aforementioned conjugated diene monomers include butadiene, 2-methyl-1,3-butadiene (hereinafter also referred to as "isoprene"), 2,3-dimethylbutadiene, 2-phenylbutadiene, 1,3-pentadiene, 2-methyl-1,3-pentadiene, 1,3-hexadiene, 1,3-octadiene, 1,3-cyclohexadiene, 2-methyl-1,3-octadiene, 1,3,7-octatriene, β-farnesene (hereinafter also referred to as "farnesene"), myrcene, and chloroprene. These conjugated dienes may be used individually or in combination of two or more. From the viewpoint of reactivity during vulcanization, it is more preferable for the conjugated diene rubber to have monomer units derived from one or more selected from butadiene, isoprene, and farnesene.

[0030] The conjugated diene rubber used in the present invention may contain units derived from other monomers besides the conjugated diene monomer, as long as they do not inhibit adhesion. Examples of other monomers include copolymerizable ethylenically unsaturated monomers and aromatic vinyl compounds. Examples of the ethylenically unsaturated monomers include ethylene, 1-butene, and olefins such as isobutylene. Examples of the aromatic vinyl compounds include styrene, α-methylstyrene, 2-methylstyrene, 3-methylstyrene, 4-methylstyrene, 4-propylstyrene, 4-t-butylstyrene, 4-cyclohexylstyrene, 4-dodecylstyrene, 2,4-dimethylstyrene, 2,4-diisopropylstyrene, 2,4,6-trimethylstyrene, 2-ethyl-4-benzylstyrene, 4-(phenylbutyl)styrene, 1-vinylnaphthalene, 2-vinylnaphthalene, vinylanthracene, N,N-diethyl-4-aminoethylstyrene, vinylpyridine, 4-methoxystyrene, monochlorostyrene, dichlorostyrene, and divinylbenzene. These may be used individually or in combination of two or more. When a conjugated diene rubber contains monomer units derived from monomers other than the conjugated diene monomer, the content is preferably 30 mol% or less, more preferably 10 mol% or less, and even more preferably 5 mol% or less.

[0031] The conjugated diene rubber used in the present invention is preferably a modified conjugated diene rubber having hydrogen-bonding functional groups in a portion of the conjugated diene rubber, and more preferably a modified conjugated diene rubber having conjugated diene units in at least a portion of the polymer chain and having hydrogen-bonding functional groups in the side chains or terminals of the polymer chain. When the modified conjugated diene rubber is used as the conjugated diene rubber, the modified conjugated diene rubber interacts with both the adherend rubber and the surface-modified fibers, thereby bonding them together. When the modified conjugated diene rubber and the adherend rubber are vulcanized to form a covalent bond, a strong cohesive force is generated, further improving adhesion. Furthermore, it is believed that the hydrogen-bonding functional groups contained in the modified conjugated diene rubber form hydrogen bonds with the surface-modified layer of the surface-modified fibers, thereby improving adhesion.

[0032] In this specification, "hydrogen bond" refers to a bonding interaction formed between a hydrogen atom (donor) that is electrically polarized by bonding to an electronegative atom (O, N, S, etc.) and an electronegative atom (acceptor) that has a lone pair of electrons.

[0033] In the present invention, "hydrogen-bonding functional group" refers to a functional group capable of functioning as a donor and acceptor in hydrogen bonding. Specifically, examples include hydroxyl groups, epoxy groups, ether groups, mercapto groups, carboxyl groups, carbonyl groups, aldehyde groups, amino groups, imino groups, imidazole groups, urethane groups, amide groups, urea groups, isocyanate groups, nitrile groups, silanol groups, and derivatives thereof. Examples of aldehyde group derivatives include their acetal derivatives. Examples of carboxyl group derivatives include their salts, esterified derivatives, amidated derivatives, and acid anhydrides. Examples of silanol group derivatives include their esterified derivatives. Examples of carboxyl groups include groups derived from monocarboxylic acids and groups derived from dicarboxylic acids. Among these, one or more selected from hydroxyl groups, epoxy groups, aldehyde groups, acetal derivatives of aldehyde groups, carboxyl groups, salts of carboxyl groups, esterified derivatives of carboxyl groups, acid anhydrides of carboxyl groups, silanol groups, esterified derivatives of silanol groups, amino groups, imidazole groups, and mercapto groups are preferred. Among these, from the viewpoint of improving adhesion and ease of manufacturing conjugated diene rubbers, one or more selected from hydroxyl groups, carboxyl groups, carbonyl groups, salts of carboxyl groups, esterified products of carboxyl groups, and acid anhydrides of carboxyl groups are preferred, one or more selected from carboxyl groups, esterified products of carboxyl groups, and acid anhydrides of carboxyl groups are more preferred, and esterified products of maleic anhydride and functional groups derived from maleic anhydride are even more preferred.

[0034] From the viewpoint of obtaining reinforcing fibers with excellent rubber adhesion, the number of hydrogen-bonding functional groups in the modified conjugated diene rubber is preferably 1 or more, more preferably 3 or more, and even more preferably 4 or more on average per molecule. Furthermore, from the viewpoint of controlling the viscosity of the modified conjugated diene rubber within an appropriate range and improving handling, the number of hydrogen-bonding functional groups is preferably 80 or less, more preferably 40 or less, even more preferably 30 or less, even more preferably 20 or less, and even more preferably 15 or less on average per molecule.

[0035] The average number of hydrogen-bonding functional groups per molecule of modified conjugated diene rubber is calculated from the equivalent weight (g / eq) of hydrogen-bonding functional groups and the number-average molecular weight (Mn) in styrene terms, based on the following formula. The equivalent weight of hydrogen-bonding functional groups in modified conjugated diene rubber refers to the mass of the conjugated diene and, if necessary, other monomers other than the conjugated diene bonded to each hydrogen-bonding functional group. Average number of hydrogen-bonding functional groups per molecule = [(number-average molecular weight (Mn)) / (molecular weight of styrene units) × (average molecular weight of conjugated dienes and other monomer units other than conjugated dienes as needed)] / (equivalent weight of hydrogen-bonding functional groups) The method for calculating the equivalent weight of hydrogen-bonding functional groups can be appropriately selected depending on the type of hydrogen-bonding functional group.

[0036] Methods for obtaining modified conjugated diene rubber include, for example, a method of obtaining it by adding a modifying compound to a polymer of a conjugated diene monomer (hereinafter also referred to as "production method (1)"), a method of obtaining it by oxidizing a conjugated diene polymer (hereinafter also referred to as "production method (2)"), a method of obtaining it by copolymerizing a conjugated diene monomer with a radical polymerizable compound having a hydrogen bonding functional group (hereinafter also referred to as "production method (3)"), and a method of adding a modifying compound that can react with the polymerization active end to an unmodified polymer of a conjugated diene monomer having a polymerization active end before adding a polymerization inhibitor (hereinafter also referred to as "production method (4)"). Among these, from the viewpoint of productivity, production by production method (1), (2), or (3) is preferred, production by production method (1) or (3) is more preferred, and production by production method (1) is even more preferred.

[0037] [Method for producing modified conjugated diene rubber (1)] Manufacturing method (1) is a method of adding a modifying compound to a polymer of conjugated diene monomers, that is, an unmodified conjugated diene rubber (hereinafter also referred to as "unmodified conjugated diene rubber"). Unmodified conjugated diene rubbers can be obtained by polymerizing a conjugated diene and, if necessary, other monomers other than the conjugated diene, for example, by emulsion polymerization or solution polymerization.

[0038] As the solution polymerization method, known or similar methods can be applied. For example, a monomer containing a predetermined amount of conjugated diene is polymerized in a solvent using a Ziegler catalyst, a metallocene catalyst, an anionically polymerizable active metal, or an active metal compound, in the presence of a polar compound as needed. Examples of solvents include aliphatic hydrocarbons such as n-butane, n-pentane, isopentane, n-hexane, n-heptane, and isooctane; alicyclic hydrocarbons such as cyclopentane, cyclohexane, and methylcyclopentane; and aromatic hydrocarbons such as benzene, toluene, and xylene.

[0039] Examples of anionically polymerizable active metals include alkali metals such as lithium, sodium, and potassium; alkaline earth metals such as beryllium, magnesium, calcium, strontium, and barium; and lanthanide rare earth metals such as lanthanum and neodymium. Among these anionically polymerizable active metals, alkali metals and alkaline earth metals are preferred, with alkali metals being more preferred. As anionically polymerizable active metal compounds, organoalkali metal compounds are preferred. Examples of organoalkali metal compounds include organomonolithium compounds such as methyllithium, ethyllithium, n-butyllithium, sec-butyllithium, t-butyllithium, hexyllithium, phenyllithium, and stilbenithium; polyfunctional organolithium compounds such as dilythiomethane, dilythionaphthalene, 1,4-dilythiobutane, 1,4-dilythio-2-ethylcyclohexane, and 1,3,5-trilythiobenzene; and sodium naphthalene and potassium naphthalene. Among these organoalkali metal compounds, organolithium compounds are preferred, and organomonolithium compounds are more preferred.

[0040] The amount of the aforementioned organoalkali metal compound used can be appropriately set according to the melt viscosity, molecular weight, etc., of the target unmodified conjugated diene rubber and modified conjugated diene rubber, but is usually used in an amount of 0.01 to 3 parts by mass per 100 parts by mass of the total monomer containing the conjugated diene. The aforementioned organoalkali metal compounds can also be reacted with secondary amines such as dibutylamine, dihexylamine, and dibenzylamine to be used as organoalkali metal amides.

[0041] Polar compounds are typically used in anionic polymerization to adjust the microstructure of the conjugated diene moiety without deactivating the reaction. Examples of polar compounds include ether compounds such as dibutyl ether, tetrahydrofuran, ethylene glycol diethyl ether, and 2,2-di(2-tetrahydrofuryl)propane; tertiary amines such as tetramethylethylenediamine and trimethylamine; alkali metal alkoxides; and phosphine compounds. Polar compounds are usually used in amounts of 0.01 to 1000 moles relative to the organoalkali metal compound. The temperature for solution polymerization is typically in the range of -80 to 150°C, preferably 0 to 100°C, and more preferably 10 to 90°C. The polymerization method may be batch or continuous. Polymerization can be stopped by adding a polymerization inhibitor. Examples of polymerization inhibitors include alcohols such as methanol and isopropanol. The unmodified conjugated diene rubber can be isolated by pouring the resulting polymerization reaction solution into a poor solvent such as methanol to precipitate the polymer, or by washing the polymerization reaction solution with water, separating the product, and drying it. Among the methods described above, solution polymerization is preferred as a method for producing unmodified conjugated diene rubber.

[0042] As the emulsion polymerization method, known or similar methods can be applied. For example, a monomer containing a predetermined amount of conjugated diene is emulsion-dispersed in the presence of an emulsifier, and emulsion polymerization is carried out with a radical polymerization initiator. Examples of emulsifiers include long-chain fatty acid salts and rosinates having 10 or more carbon atoms. Examples of long-chain fatty acid salts include potassium or sodium salts of fatty acids such as capric acid, lauric acid, myristic acid, palmitic acid, oleic acid, and stearic acid. Water is typically used as the dispersion solvent, and water-soluble organic solvents such as methanol and ethanol may also be included, as long as they do not impair the stability during polymerization. Examples of radical polymerization initiators include persulfates such as ammonium persulfate and potassium persulfate, organic peroxides, and hydrogen peroxide. To adjust the molecular weight of the resulting unmodified conjugated diene rubber, a chain transfer agent may be used. Examples of chain transfer agents include mercaptans such as t-dodecyl mercaptan and n-dodecyl mercaptan; carbon tetrachloride, thioglycolic acid, diterpenes, terpinolene, γ-terpinene, and α-methylstyrene dimer.

[0043] The emulsion polymerization temperature can be set appropriately depending on the type of radical polymerization initiator used, but is usually in the range of 0 to 100°C, preferably 0 to 60°C. The polymerization method can be either continuous polymerization or batch polymerization.

[0044] Polymerization reactions can be stopped by adding polymerization inhibitors. Examples of polymerization inhibitors include amine compounds such as isopropylhydroxylamine, diethylhydroxylamine, and hydroxylamine, quinone compounds such as hydroquinone and benzoquinone, and sodium nitrite.

[0045] After the polymerization reaction is stopped, an antioxidant may be added as needed. After the polymerization reaction is stopped, unreacted monomers are removed from the obtained latex as needed, and then, using salts such as sodium chloride, calcium chloride, and potassium chloride as a coagulant, the polymer is solidified while adjusting the pH of the coagulation system to a predetermined value by adding acids such as nitric acid and sulfuric acid as needed. After solidification, the polymer is recovered by separating the dispersion solvent. Then, after washing with water and dehydration, the unmodified conjugated diene rubber is obtained by drying. Alternatively, during solidification, the latex may be mixed with an emulsified dispersion of spreading oil beforehand, and recovered as oil-expanded unmodified conjugated diene rubber.

[0046] (Modified compound used in manufacturing method (1)) There are no particular restrictions on the modified compound used in manufacturing method (1), but from the viewpoint of improving the adhesion of reinforcing fibers, it is preferable to use one that has a hydrogen bonding functional group. Examples of hydrogen bonding functional groups are those described above. Among these, from the viewpoint of the strength of hydrogen bonding, amino groups, imidazole groups, urea groups, hydroxyl groups, epoxy groups, mercapto groups, silanol groups, aldehyde groups, carboxyl groups and their derivatives are preferred. As derivatives of the carboxyl group, salts thereof, esterified products thereof, amidated products thereof, or acid anhydrides thereof are preferred. These modified compounds having hydrogen bonding functional groups may be used individually or in combination of two or more.

[0047] Examples of the modified compounds include unsaturated carboxylic acids such as maleic acid, fumaric acid, citraconic acid, and itaconic acid; unsaturated carboxylic acid anhydrides such as maleic anhydride, citraconic anhydride, 2,3-dimethylmaleic anhydride, and itaconic anhydride; unsaturated carboxylic acid esters such as maleic acid esters, fumaric acid esters, citraconic acid esters, and itaconic acid esters; unsaturated carboxylic acid amides such as maleic acid amide, fumaric acid amide, citraconic acid amide, and itaconic acid amide; unsaturated carboxylic acid imides such as maleic acid imide, fumaric acid imide, citraconic acid imide, and itaconic acid imide; vinyltrimethoxysilane, γ-methacryloxypropyltrimethoxysilane, mercaptomethylmethyldi Examples of silane compounds include ethoxysilane, mercaptomethyltriethoxysilane, 2-mercaptoethyltrimethoxysilane, 2-mercaptoethyltriethoxysilane, 2-mercaptoethylmethoxydimethylsilane, 2-mercaptoethylethoxydimethylsilane, 3-mercaptopropyltrimethoxysilane, 3-mercaptopropyltriethoxysilane, 3-mercaptopropyldimethoxymethylsilane, 3-mercaptopropyldiethoxymethylsilane, 3-mercaptopropyldimethoxyethylsilane, 3-mercaptopropyldiethoxyethylsilane, 3-mercaptopropylmethoxydimethylsilane, and 3-mercaptopropylethoxydimethylsilane.

[0048] The amount of the modified compound used is preferably 0.1 to 100 parts by mass, more preferably 0.5 to 50 parts by mass, and even more preferably 1 to 30 parts by mass, per 100 parts by mass of the unmodified conjugated diene rubber. The reaction temperature is usually preferably in the range of 0 to 200°C, and more preferably in the range of 50 to 200°C. Alternatively, after grafting the modified compound onto an unmodified conjugated diene rubber to introduce hydrogen-bonding functional groups, another modified compound that can react with these functional groups may be added to introduce another hydrogen-bonding functional group into the polymer. Specifically, for example, an unmodified conjugated diene rubber obtained by living anionic polymerization may be grafted with maleic anhydride, and then reacted with compounds having hydroxyl groups such as 2-hydroxyethyl methacrylate or methanol, or with water.

[0049] The amount of modified compound added to modified conjugated diene rubber is preferably 0.5 to 40 parts by mass, more preferably 1 to 30 parts by mass, and even more preferably 1.5 to 20 parts by mass, per 100 parts by mass of unmodified conjugated diene rubber. The amount of modified compound added to the modified conjugated diene rubber can be calculated based on the acid value of the modified compound, or it can be determined using various analytical instruments such as infrared spectroscopy and nuclear magnetic resonance spectroscopy.

[0050] The method for adding the modified compound to the unmodified conjugated diene rubber is not particularly limited. For example, a method can be used in which liquid unmodified conjugated diene rubber is heated in the presence or absence of an organic solvent by adding one or more modified compounds selected from unsaturated carboxylic acids, unsaturated carboxylic acid derivatives, and silane compounds, and optionally a radical generator. There are no particular restrictions on the radical generator used, and commercially available organic peroxides, azo compounds, hydrogen peroxide, etc., can be used. The organic solvents used in the above method generally include hydrocarbon solvents and halogenated hydrocarbon solvents. Among these organic solvents, hydrocarbon solvents such as n-butane, n-hexane, n-heptane, cyclohexane, benzene, toluene, and xylene are preferred.

[0051] Furthermore, when carrying out the reaction to add the modified compound by the method described above, an antioxidant may be added to suppress side reactions. Commercially available antioxidants can be used, such as butylated hydroxytoluene (BHT) and N-phenyl-N'-(1,3-dimethylbutyl)-p-phenylenediamine (Nocrack 6C). The amount of antioxidant added is preferably 0.01 to 10 parts by mass, and more preferably 0.05 to 5 parts by mass, per 100 parts by mass of unmodified conjugated diene rubber. When the amount of antioxidant added is within the above range, side reactions can be suppressed, and modified conjugated diene rubber can be obtained in good yield.

[0052] [Physical properties of conjugated diene rubbers] The weight-average molecular weight (Mw) of the conjugated diene rubber is not particularly limited, but from the viewpoint of improving adhesion, it is preferably greater than 2,000, more preferably 5,000 or more, even more preferably 10,000 or more, even more preferably 15,000 or more, even more preferably 20,000 or more, and especially preferably 25,000 or more. From the viewpoint of ease of handling, it is preferably 120,000 or less, more preferably 100,000 or less, even more preferably 75,000 or less, and even more preferably 55,000 or less.

[0053] The number-average molecular weight (Mn) of the conjugated diene rubber is not particularly limited, but from the viewpoint of improving adhesion, it is preferably 2,000 or more, more preferably 5,000 or more, even more preferably 10,000 or more, even more preferably 15,000 or more, even more preferably 20,000 or more, and particularly preferably 25,000 or more. From the viewpoint of ease of handling, it is preferably 120,000 or less, more preferably 75,000 or less, even more preferably 50,000 or less, and even more preferably 47,000 or less. The Mw and Mn of the conjugated diene rubber are the weight-average molecular weight and number-average molecular weight in polystyrene terms, determined from gel permeation chromatography (GPC) measurements, and can be specifically measured by the method described in the examples.

[0054] The molecular weight distribution (Mw / Mn) of the conjugated diene rubber is preferably 1.00 to 5.00, more preferably 1.00 to 3.00, even more preferably 1.00 to 2.00, even more preferably 1.00 to 1.50, and particularly preferably 1.00 to 1.30. When Mw / Mn is within the above range, the viscosity variation of the conjugated diene rubber is small, making it easy to handle. The molecular weight distribution (Mw / Mn) refers to the ratio of the weight-average molecular weight (Mw) to the number-average molecular weight (Mn) on a standard polystyrene basis, determined by GPC measurement.

[0055] Furthermore, from the viewpoint of adhesion between the conjugated diene rubber and the fiber, it is preferable that the conjugated diene rubber be in liquid form. In this specification, "liquid" means that the melt viscosity of the conjugated diene rubber measured at 38°C is 4,000 Pa·s or less. From the viewpoint of improving adhesion, the melt viscosity is preferably 0.1 Pa·s or more, more preferably 1 Pa·s or more, even more preferably 10 Pa·s or more, even more preferably 30 Pa·s or more, and even more preferably 50 Pa·s or more. From the viewpoint of handling, it is preferably 2,500 Pa·s or less, and even more preferably 2,100 Pa·s or less. When the melt viscosity is within the above range, the handling properties of the conjugated diene rubber can be improved while maintaining good adhesion. Note that the melt viscosity of conjugated diene rubber refers to the viscosity measured at 38°C using a Brookfield type viscometer (Type B viscometer).

[0056] The glass transition temperature (Tg) of conjugated diene rubber can vary depending on the vinyl content of the conjugated diene units, the type of conjugated diene, and the content of units derived from other monomers besides the conjugated diene, but is preferably -100 to 10°C, more preferably -100 to 0°C, and even more preferably -100 to -10°C. When Tg is within the above range, viscosity increases can be suppressed and handling becomes easier.

[0057] The vinyl content of the conjugated diene rubber is preferably 80 mol% or less, more preferably 50 mol% or less, and even more preferably 30 mol% or less. Adhesion is improved when the vinyl content is within the above range. In this specification, "vinyl content" means the total mole percent of conjugated diene units (conjugated diene units linked by 1,2-bonds or 3,4-bonds, other than 1,4-bonds) out of a total of 100 mole percent of conjugated diene units contained in the modified liquid diene rubber. 1 It can be calculated using 1H-NMR by taking the integral ratio of the signals originating from conjugated diene units linked by 1,2-bonds or 3,4-bonds and the signals originating from conjugated diene units linked by 1,4-bonds.

[0058] 〔oil〕 The adhesive layer in the present invention can be formed, for example, by applying an adhesive component consisting of a solution obtained by dissolving a conjugated diene rubber in oil to a surface-modified fiber. In the present invention, it is preferable to use a so-called non-volatile oil, for example, one whose vapor pressure at 20°C is 10 Pa or less. By using such an oil, the oil does not evaporate for a long period of time even after the adhesive component is applied to the surface of the fiber, so uneven application of the adhesive component is less likely to occur, and the adhesiveness is improved. Furthermore, contamination of the manufacturing equipment during manufacturing can be suppressed. From these viewpoints, the oil is preferably one whose vapor pressure at 20°C is 8 Pa or less, more preferably 5 Pa or less, even more preferably 1 Pa or less, even more preferably 0.1 Pa or less, and even more preferably 0.01 Pa or less. In this invention, the vapor pressure of the oil at 20°C refers to the value calculated using the optimal curve obtained by applying the Antoine equation to the measured value obtained by the gas flow method. In the present invention, when oil is used, a heating step for resin formation is unnecessary compared to conventional techniques using RFL, and furthermore, an evaporation step to remove water or other solvents is unnecessary compared to conventional techniques using water or other solvents as diluents. Therefore, it is possible to manufacture efficiently with simpler equipment compared to conventional methods, and it is also environmentally friendly.

[0059] The oils that can be used in the present invention, having a vapor pressure of 10 Pa or less at 20°C, are not particularly limited as long as they are compatible with conjugated diene rubber, but examples include natural oils and synthetic oils. Examples of natural oils include mineral oils and vegetable oils. Examples of mineral oils include paraffinic mineral oils, aromatic mineral oils, and naphthenic mineral oils obtained by conventional refining methods such as solvent refining and hydrogenation refining, as well as waxes (gastriq waxes) produced by processes such as the Fischer-Tropsch process, and mineral oils produced by isomerizing waxes. Examples of commercially available paraffinic mineral oils include the "Diana Process Oil" series from Idemitsu Kosan Co., Ltd. and the "Super Oil" series from JX Energy Corporation. Examples of vegetable oils include linseed oil, camellia oil, macadamia nut oil, corn oil, mink oil, olive oil, avocado oil, sasanqua oil, castor oil, safflower oil, jojoba oil, sunflower oil, almond oil, rapeseed oil, sesame oil, soybean oil, peanut oil, cottonseed oil, coconut oil, palm kernel oil, and rice bran oil. Examples of synthetic oils include hydrocarbon-based synthetic oils, ester-based synthetic oils, and ether-based synthetic oils. Examples of hydrocarbon-based synthetic oils include polybutene, polyisobutylene, 1-octene oligomer, 1-decene oligomer, and α-olefin oligomers or their hydrogenates such as ethylene-propylene copolymers, alkylbenzenes, and alkylnaphthalenes. Examples of ester-based synthetic oils include triglycerin fatty acid esters, diglycerin fatty acid esters, monoglycerin fatty acid esters, monoalcohol fatty acid esters, and polyhydric alcohol fatty acid esters. Examples of ether-based synthetic oils include polyoxyalkylene glycol and polyphenyl ethers. Examples of commercially available synthetic oils include the "Linearene" series from Idemitsu Kosan Co., Ltd., and "FGC32," "FGC46," and "FGC68" from ANDEROL.

[0060] The oil may be one selected from the aforementioned natural oils and synthetic oils, or it may be a mixture of two or more natural oils, two or more synthetic oils, or one or more natural oils and one or more synthetic oils. In the present invention, from the viewpoint of setting the viscosity of the adhesive component within an appropriate range and improving workability, mineral oil is preferred, and at least one selected from paraffinic mineral oil and naphthenic mineral oil is more preferred.

[0061] From a safety standpoint, the flash point of the oil used in this invention is preferably 70°C or higher. From this standpoint, the flash point of the oil is more preferably 100°C or higher, even more preferably 130°C or higher, and even more preferably 140°C or higher. There is no particular upper limit to the flash point of the oil, but it is preferably 320°C or lower.

[0062] The content of conjugated diene rubber in the adhesive component is preferably 1% by mass or more, more preferably 5% by mass or more, even more preferably 10% by mass or more, and preferably 80% by mass or less, more preferably 60% by mass or less, even more preferably 50% by mass or less, and even more preferably 40% by mass or less, from the viewpoint of improving the adhesive strength with rubber. When the content of conjugated diene rubber in the adhesive component is within the above range, it is possible to obtain sufficient adhesive strength while preventing the viscosity of the adhesive component from becoming extremely high. Furthermore, the oil content in the adhesive component is preferably 20% by mass or more, more preferably 40% by mass or more, even more preferably 50% by mass or more, and even more preferably 60% by mass or more, and preferably 99% by mass or less, more preferably 95% by mass or less, and even more preferably 90% by mass or less.

[0063] The mass ratio of conjugated diene rubber to oil in the adhesive component [conjugated diene rubber (R): oil (O)] is preferably 0.1:9.9 to 8:2, more preferably 0.5:9.5 to 6:4, even more preferably 1:9 to 5:5, and even more preferably 1:9 to 4:6. Although oil is generally known to worsen the adhesion of rubber, when conjugated diene rubber and oil are mixed and used in the above-mentioned specific mass ratio, it is possible to reduce viscosity while maintaining adhesion, improving the handling of the adhesive component and also improving the adhesion workability to surface-modified fibers.

[0064] In addition, in the present invention, an adhesive layer may be formed by attaching an adhesive component consisting of an emulsion obtained by dispersing the conjugated diene rubber in water to the surface-modified fibers. When using a conjugated diene rubber dispersed in water as an oil-in-water emulsion, it is preferable to prepare the adhesive emulsion (latex) in advance by mechanical or chemical means and use it at a predetermined concentration by dilution or other means. Mechanical methods include the use of homogenizers, homomixers, disperser mixers, colloid mills, pipeline mixers, high-pressure homogenizers, ultrasonic emulsifiers, etc., which can be used individually or in combination. Various chemical methods can be used, including the inversion emulsification method, D-phase emulsification method, HLB temperature emulsification method, gel emulsification method, and liquid crystal emulsification method. The inversion emulsification method is preferred from the viewpoint of easily obtaining an emulsion with fine particle size. In addition, in order to obtain an emulsion with fine particle size, it may be preferable to carry out the work while heating at an appropriate temperature (e.g., 30-80°C) in order to lower the viscosity of the modified conjugated diene rubber.

[0065] When the adhesive component is an emulsion, the content of conjugated diene rubber in the adhesive component is preferably 0.5% by mass or more, more preferably 1% by mass or more, even more preferably 2% by mass or more, and preferably 60% by mass or less, more preferably 40% by mass or less, even more preferably 30% by mass or less, and even more preferably 20% by mass or less, from the viewpoint of improving the adhesive strength with rubber. When the content of conjugated diene rubber in the adhesive component is within the above range, it is possible to obtain sufficient adhesive strength while preventing the viscosity of the adhesive component from becoming extremely high.

[0066] The aforementioned conjugated diene rubber may be used alone or in combination of two or more types. Similarly, the aforementioned oil may be used alone or in combination of two or more types.

[0067] Furthermore, the adhesive component in the present invention may include other components besides conjugated diene rubber and oil, as long as they do not impede the adhesive strength with rubber. Other components include other polymers (e.g., unmodified conjugated diene rubber), acids, alkalis, antioxidants, curing agents, dispersants, pigments, dyes, adhesives, carbon black, etc. If the adhesive component contains other components, the amount thereof is preferably 10,000 parts by mass or less, more preferably 1,000 parts by mass or less, even more preferably 100 parts by mass or less, even more preferably 50 parts by mass or less, even more preferably 25 parts by mass or less, and even more preferably 10 parts by mass or less, per 100 parts by mass of the conjugated diene rubber.

[0068] [Method for manufacturing reinforcing fibers] There are no particular limitations on the method for producing the reinforcing fibers of the present invention, and they can be produced by a method that includes a step of attaching the conjugated diene rubber to the fibers in a state mixed with the oil, or a step of attaching the conjugated diene rubber to the fibers in a state dispersed in water. In the present invention, from the viewpoint of efficiently adhering the conjugated diene rubber to the surface-modified fibers and from the viewpoint of suppressing contamination of the manufacturing equipment, a method including the step of adhering the conjugated diene rubber to the fibers in a state mixed with the oil is preferred. More specific methods for producing the reinforcing fibers of the present invention include the following methods.

[0069] [Method (I)] Method (I) is not particularly limited as long as it is a method of forming an adhesive layer consisting of the adhesive component on the surface of the surface-modified fiber, but from the viewpoint of improving adhesion to rubber, a method including the following step I-1 is preferred. Step I-1: Step of attaching the adhesive component to the surface of the surface-modified fiber.

[0070] In step I-1, there are no particular restrictions on the method of attaching the adhesive component to the surface-modified fibers. Examples include attaching the adhesive component as is, or adding a solvent to the adhesive component as needed before attaching it. It is preferable to apply the adhesive component by one or more methods selected from immersion, roll coater, oiling roller, oiling guide, nozzle (spray) application, and brush application.

[0071] From the viewpoint of improving the adhesion between the reinforcing fibers and the rubber, the amount of adhesive component to be attached is preferably 0.01 parts by mass or more, more preferably 0.1 parts by mass or more, and even more preferably 1 part by mass or more, per 100 parts by mass of the fibers used as raw material. From the viewpoint of balancing manufacturing costs and effects, it is preferably 10 parts by mass or less, more preferably 5 parts by mass or less, and even more preferably 3 parts by mass or less.

[0072] In the present invention, when a conjugated diene rubber and a specific oil are used in combination, the reinforcing fibers of the present invention can be obtained by attaching the adhesive component to the surface-modified fibers and then allowing them to settle at room temperature of about 20°C for about 3 to 10 days. However, in some cases, the following step I-2 may be performed. Step I-2: A step of heat-treating the surface-modified fibers to which the adhesive component obtained in Step I-1 has been attached. The heat treatment in step I-2 is preferably carried out at a treatment temperature of 100 to 200°C for a treatment time of 0.1 seconds to 2 minutes. Since the conjugated diene rubber contained in the adhesive component has reactive multiple bonds, the heat treatment in the presence of oxygen is preferably 200°C or lower, and more preferably 175°C or lower. When the heat treatment temperature is within the above range, the amount of reactive multiple bonds in the conjugated diene rubber does not decrease, the adhesive strength can be improved, and furthermore, fiber deterioration is suppressed, and quality such as coloring is also improved.

[0073] The reinforcing fibers may contain other components besides the surface-modifying fibers and the adhesive components. Examples of other components include crosslinking agents, acids, bases, inorganic salts, organic salts, pigments, dyes, antioxidants, polymerization initiators, and plasticizers. The total content of the hydrophilic fibers and adhesive components in the reinforcing fibers is preferably 80% by mass or more, more preferably 90% by mass or more, and even more preferably 95% by mass or more, from the viewpoint of improving adhesion to rubber and reinforcing strength.

[0074] <Physical properties of reinforcing fibers> The reinforcing fiber is preferably a multifilament with a single filament fineness of 0.1 dtex or more and 30 dtex or less. The single filament fineness may be less than 0.1 dtex, but since it is difficult to manufacture industrially, 0.1 dtex or more is preferred. Furthermore, when the single filament fineness is 30 dtex or less, the surface area of ​​the fiber when used as a reinforcing fiber increases, which improves adhesion to rubber. From this viewpoint, the reinforcing fiber of the present invention is preferably a multifilament with a single filament fineness of more preferably 0.3 dtex or more, even more preferably 0.5 dtex or more, even more preferably 1 dtex or more, and more preferably 20 dtex or less, even more preferably 15 dtex or less, and even more preferably 10 dtex or less.

[0075] The rubber adhesive strength of the reinforcing fibers of the present invention is preferably 30 N / 25.4 mm or more, more preferably 50 N / 25.4 mm or more, even more preferably 70 N / 25.4 mm or more, even more preferably 80 N / 25.4 mm or more, and usually 200 N / 25.4 mm or less. When the rubber adhesive strength of the reinforcing fibers is above the above lower limit, woven fabrics, knitted fabrics, and molded articles with excellent reinforcing strength can be obtained. Furthermore, the rubber adhesive strength of the reinforcing fibers of the present invention is preferably 30 N / 3 strands or more, more preferably 40 N / 3 strands or more, even more preferably 50 N / 3 strands or more, and even more preferably 60 N / 3 strands or more, and is usually 200 N / 3 strands or less. When the rubber adhesive strength of the reinforcing fibers is above the above lower limit, woven fabrics, knitted fabrics and molded articles with excellent reinforcing strength can be obtained. The rubber adhesive strength of the reinforcing fibers can be measured by the method described in the examples.

[0076] The reinforcing fibers of the present invention can be used in any shape, but it is preferable to use them in the form of a fiber cord, woven fabric, knitted fabric, etc., which contain at least a portion of the reinforcing fibers, and it is more preferable to use them as a woven fabric or knitted fabric which contains at least a portion of the reinforcing fibers. For example, as described later, they can be used as a knitted fabric to be bonded to rubber. They can also be used as reinforcing fibers to be embedded in resin, cement, etc.

[0077] [Molded body] The molded article of the present invention is not particularly limited as long as it uses the reinforcing fibers. In particular, a molded article having the reinforcing fibers and a rubber layer (hereinafter also referred to as a "rubber molded article") is preferred because the reinforcing fibers have excellent adhesion to rubber. From the viewpoint of maintaining the shape of the rubber, the reinforcing fibers used in the rubber molded article are preferably used as a woven or knitted fabric containing at least a portion of the reinforcing fibers, and more preferably as a laminate in which a reinforcing layer made of a woven or knitted fabric containing at least a portion of the reinforcing fibers and a rubber layer are laminated together. A preferred embodiment of the molded article of the present invention is a molded article having, in this order, fibers, a surface modification layer, an adhesive layer, and a rubber layer, wherein the adhesive strength between the adhesive layer and the rubber layer is preferably 70 N or more per 25.4 mm width, more preferably 80 N or more, and if the adhesive strength is 70 N or more, it can be suitably used for various applications described later.

[0078] The aforementioned rubber molded body can be used as a component of rubber products such as tires for automobiles, belts such as conveyor belts and timing belts, hoses, and vibration-damping rubber, and is more preferably used as a tire, belt, or hose. The aforementioned automobile tires can be used for various components, such as belts, carcass plies, breakers, and bead tapes, which are composite materials of reinforcing fibers and rubber components. The hose can be used for transporting various fluids in various applications, and is particularly suitable as a fluid transport hose for automobiles, and is especially preferred for use as a liquid fuel hose, brake oil hose, and refrigerant hose for automobiles, and more preferably as a brake oil hose for automobiles.

[0079] Preferably, the rubber molded article is formed using the reinforcing fibers and a rubber composition in which a compounding agent commonly used in the rubber industry is blended with the rubber component. The rubber components are not particularly limited, but examples include NR (natural rubber), IR (polyisoprene rubber), BR (polybutadiene rubber), SBR (styrene-butadiene rubber), NBR (nitrile rubber), EPM (ethylene-propylene copolymer rubber), EPDM (ethylene-propylene-non-conjugated diene copolymer rubber), IIR (butyl rubber), halogenated butyl rubber, and CR (chloroprene rubber). Among these, NR, IR, BR, SBR, EPDM, and CR are preferred, and EPDM is more preferred. These rubber components may be used individually or in combination of two or more. For tire applications, those commonly used in the tire industry can be used. Among these, natural rubber alone or a combination of natural rubber and SBR is preferred. When combining natural rubber and SBR, from the viewpoint of suppressing the deterioration of physical properties due to the re-vulcanization of the rubber, the mass ratio of natural rubber to SBR (natural rubber / SBR) is preferably in the range of 50 / 50 to 90 / 10.

[0080] Examples of the aforementioned natural rubber include TSR (Technically Specified Rubber) such as SMR (Malaysian TSR), SIR (Indonesian TSR), and STR (Thai TSR), as well as RSS (Ribbed Smoked Sheet), which are commonly used in the tire industry, and modified natural rubbers such as high-purity natural rubber, epoxidized natural rubber, hydroxylated natural rubber, hydrogenated natural rubber, and grafted natural rubber.

[0081] As for the aforementioned SBR, a general type used in tire applications can be used, but specifically, one with a styrene content of 0.1 to 70% by mass is preferred, one with a styrene content of 5 to 50% by mass is more preferred, and one with a styrene content of 15 to 35% by mass is even more preferred. Furthermore, one with a vinyl content of 0.1 to 60% by mass is preferred, and one with a vinyl content of 0.1 to 55% by mass is even more preferred. The weight-average molecular weight (Mw) of the SBR is preferably between 100,000 and 2,500,000, more preferably between 150,000 and 2,000,000, and even more preferably between 200,000 and 1,500,000. When the molecular weight is within this range, both processability and mechanical strength can be achieved. The weight-average molecular weight of the SBR is the weight-average molecular weight on a polystyrene basis, determined from gel permeation chromatography (GPC) measurements. As the SBR mentioned above, modified SBR in which a functional group has been introduced may be used, as long as it does not impair the effects of the present invention. Examples of functional groups include amino groups, alkoxysilyl groups, hydroxyl groups, epoxy groups, carboxyl groups, and the like.

[0082] The rubber composition may further contain fillers in addition to the rubber components. Examples of such fillers include inorganic fillers such as carbon black, silica, clay, mica, calcium carbonate, magnesium hydroxide, aluminum hydroxide, barium sulfate, titanium dioxide, glass fibers, fibrous fillers, and glass balloons; and organic fillers such as resin particles, wood powder, and cork powder. The inclusion of such fillers in the rubber composition makes it possible to improve physical properties such as mechanical strength, heat resistance, or weather resistance, adjust hardness, and increase the amount of rubber. From the viewpoint of improving physical properties such as increased mechanical strength, carbon black and silica are preferred among the fillers mentioned above.

[0083] Examples of the aforementioned carbon black include furnace black, channel black, thermal black, acetylene black, and Ketjen black. From the viewpoint of improving crosslinking speed and mechanical strength, furnace black is preferred among these carbon blacks. The average particle size of the carbon black is preferably 5 to 100 nm, more preferably 5 to 80 nm, and even more preferably 5 to 70 nm. The average particle size of the carbon black can be determined by measuring the diameter of the particles using a transmission electron microscope and calculating the average value.

[0084] Examples of the aforementioned silica include wet silica (hydrated silica), dry silica (anhydrous silica), calcium silicate, and aluminum silicate. Among these silicas, wet silica is preferred. The average particle size of the silica is preferably 0.5 to 200 nm, more preferably 5 to 150 nm, and even more preferably 10 to 100 nm. The average particle size of the silica can be determined by measuring the particle diameter using a transmission electron microscope and calculating the average value.

[0085] In the rubber composition, the content of the filler per 100 parts by mass of the rubber component is preferably 20 to 150 parts by mass, more preferably 25 to 130 parts by mass, and even more preferably 25 to 110 parts by mass. Furthermore, when a filler other than silica and carbon black is used as the filler, its content is preferably 20 to 120 parts by mass, more preferably 20 to 90 parts by mass, and even more preferably 20 to 80 parts by mass, per 100 parts by mass of the rubber component. These fillers may be used individually or in combination of two or more types.

[0086] The rubber composition may further contain a crosslinking agent to crosslink the rubber component. Examples of the crosslinking agent include sulfur, sulfur compounds, oxygen, organic peroxides, phenolic resins, amino resins, quinones and quinone dioxime derivatives, halogen compounds, aldehyde compounds, alcohol compounds, epoxy compounds, metal halides and organometallic halides, and silane compounds. These crosslinking agents may be used individually or in combination of two or more. From the viewpoint of the mechanical properties of the crosslinked product, the crosslinking agent is usually contained in an amount of 0.1 to 10 parts by mass, preferably 0.5 to 10 parts by mass, and more preferably 0.8 to 5 parts by mass, per 100 parts by mass of the rubber component.

[0087] The rubber composition may further contain a vulcanization accelerator if it contains, for example, sulfur, sulfur compounds, etc., as a crosslinking agent for crosslinking (vulcanizing) the rubber component. Examples of the vulcanization accelerator include guanidine compounds, sulfenamide compounds, thiazole compounds, thiram compounds, thiourea compounds, dithiocarbamate compounds, aldehyde-amine compounds, aldehyde-ammonia compounds, imidazoline compounds, and xanthate compounds. These vulcanization accelerators may be used individually or in combination of two or more. The vulcanization accelerator is usually contained in an amount of 0.1 to 15 parts by mass, preferably 0.1 to 10 parts by mass, per 100 parts by mass of the rubber component.

[0088] The rubber composition may further contain a vulcanization aid if it contains, for example, sulfur, sulfur compounds, etc., as a crosslinking agent for crosslinking (vulcanizing) the rubber component. Examples of the vulcanization aid include fatty acids such as stearic acid, metal oxides such as zinc oxide, and fatty acid metal salts such as zinc stearate. These vulcanization aids may be used individually or in combination of two or more. The vulcanization aid is usually contained in an amount of 0.1 to 15 parts by mass, preferably 1 to 10 parts by mass, per 100 parts by mass of the rubber component.

[0089] If the rubber composition contains silica as a filler, it is preferable to further contain a silane coupling agent. Examples of silane coupling agents include sulfide compounds, mercapto compounds, vinyl compounds, amino compounds, glycidoxy compounds, nitro compounds, chloro compounds, and the like. These silane coupling agents may be used individually or in combination of two or more. The silane coupling agent is preferably contained in an amount of 0.1 to 30 parts by mass, more preferably 0.5 to 20 parts by mass, and even more preferably 1 to 15 parts by mass, per 100 parts by mass of silica. When the content of the silane coupling agent is within the above range, dispersibility, coupling effect, and reinforcing properties are improved.

[0090] The rubber composition may, to the extent that it does not impede the effects of the present invention, optionally contain softeners such as process oils including silicone oil, aroma oil, TDAE (Treated Distilled Aromatic Extracts), MES (Mild Extracted Solvates), RAE (Residual Aromatic Extracts), paraffin oil, naphthenic oil, aliphatic hydrocarbon resins, alicyclic hydrocarbon resins, C9 resins, rosin resins, coumarone-indene resins, and phenolic resins, for the purpose of improving processability, fluidity, etc. If the rubber composition contains the process oil as a softener, the amount is preferably less than 50 parts by mass per 100 parts by mass of the rubber component.

[0091] The rubber composition may contain additives such as antioxidants, waxes, antioxidants, lubricants, light stabilizers, scorch inhibitors, processing aids, colorants such as pigments and dyes, flame retardants, antistatic agents, matting agents, antiblocking agents, ultraviolet absorbers, mold release agents, foaming agents, antibacterial agents, antifungal agents, and fragrances, as needed, to improve weather resistance, heat resistance, oxidation resistance, etc., to the extent that they do not impair the effects of the present invention. Examples of antioxidants include hindered phenol compounds, phosphorus compounds, lactone compounds, and hydroxyl compounds. Examples of antioxidants include amine-ketone compounds, imidazole compounds, amine compounds, phenol compounds, sulfur compounds, and phosphorus compounds. These additives may be used individually or in combination of two or more.

[0092] As a method for manufacturing the rubber molded article, for example, the reinforcing fibers are embedded in the unvulcanized rubber composition, and the rubber composition is vulcanized to obtain a molded article in which the surface-modified fibers and the rubber component are bonded together via the adhesive component.

[0093] Examples of the aforementioned brake oil hose for automobiles include one having an inner rubber layer and an outer rubber layer, with one or two reinforcing layers made of the reinforcing fibers between the inner rubber layer and the outer rubber layer. The rubber components that make up the inner rubber layer and the outer rubber layer are as described above. In particular, the rubber components that make up the inner rubber layer include EPDM and SBR, and the rubber components that make up the outer rubber layer include EPDM and CR. The reinforcing layer can be formed by braiding reinforcing fibers. As a method for manufacturing the brake oil hose, a reinforcing layer (first reinforcing layer) made of braided reinforcing fibers is formed on the outer surface of the inner rubber layer. When forming two reinforcing layers, an intermediate rubber layer may be further formed on the outer surface of the first reinforcing layer, and a reinforcing layer (second reinforcing layer) made of braided reinforcing fibers may be formed on the outer surface of the intermediate rubber layer. Then, an outer rubber layer is formed on the outer surface of the reinforcing layer (first reinforcing layer or second reinforcing layer), and the hose can be manufactured by vulcanization. The vulcanization temperature can be appropriately selected depending on the type of constituent material of each layer of the brake oil hose, but it is preferable to set it to 200°C or lower from the viewpoint of suppressing deterioration of the rubber and reinforcing fibers and improving the adhesion between the rubber and reinforcing fibers. [Examples]

[0094] The present invention will be described in more detail below with reference to examples, but the present invention is not limited in any way by such examples.

[0095] <Manufacturing of Modified Conjugated Diene Rubber> • Manufacture of modified conjugated diene rubber having monomer units represented by the following formula (1a) [ka]

[0096] Manufacturing Example 1: Manufacturing of Modified Conjugated Diene Rubber (A-1) A thoroughly dried 5 L autoclave was purged with nitrogen, and 756 g of hexane and 122.3 g of n-butyllithium (17% by mass hexane solution) were charged. After raising the temperature to 50°C, 1344 g of butadiene was added sequentially under stirring conditions, while controlling the polymerization temperature to 50°C, and polymerization was carried out for 1 hour. Methanol was then added to stop the polymerization reaction and obtain a polymer solution. Water was added to the obtained polymer solution and stirred, and the polymer solution was washed with water. After stopping the stirring and confirming that the polymer solution phase and the aqueous phase had separated, the water was separated. The polymer solution after washing was vacuum dried at 70°C for 24 hours to obtain unmodified liquid polybutadiene (A'-1). Next, 600 g of the obtained unmodified liquid polybutadiene (A'-1) was charged into a 1 L autoclave that had been purged with nitrogen. 30 g of maleic anhydride and 0.6 g of N-phenyl-N'-(1,3-dimethylbutyl)-p-phenylenediamine (trade name "Nocrac 6C", manufactured by Ouchi Shinko Chemical Industry Co., Ltd.) were added, and the mixture was reacted at 170°C for 24 hours to obtain maleic anhydride-modified liquid polybutadiene (A-1).

[0097] Manufacturing Example 2: Manufacturing of Modified Conjugated Diene Rubber (A-2) A thoroughly dried 5L autoclave was purged with nitrogen, and 1260g of hexane and 36.3g of n-butyllithium (17% by mass hexane solution) were charged. After raising the temperature to 50°C, 1260g of butadiene was added sequentially under stirring conditions, while controlling the polymerization temperature to 50°C, and polymerization was carried out for 1 hour. Methanol was then added to stop the polymerization reaction and obtain a polymer solution. Water was added to the obtained polymer solution and stirred, and the polymer solution was washed with water. After stopping the stirring and confirming that the polymer solution phase and the aqueous phase had separated, the water was separated. The polymer solution after washing was vacuum dried at 70°C for 24 hours to obtain unmodified liquid polybutadiene (A'-2). Next, 500g of the obtained unmodified liquid polybutadiene (A'-2) was charged into a 1L autoclave that had been purged with nitrogen. 25g of maleic anhydride and 0.5g of N-phenyl-N'-(1,3-dimethylbutyl)-p-phenylenediamine (trade name "Nocrac 6C", manufactured by Ouchi Shinko Chemical Industry Co., Ltd.) were added, and the mixture was reacted at 170°C for 24 hours to obtain maleic anhydride-modified liquid polybutadiene (A'-2).

[0098] Manufacturing Example 3: Manufacturing of Modified Conjugated Diene Rubber (A-3) A thoroughly dried 5 L autoclave was purged with nitrogen, and 1140 g of hexane and 20.9 g of n-butyllithium (17% by mass hexane solution) were charged. After raising the temperature to 50°C, 1390 g of butadiene was added sequentially under stirring conditions, while controlling the polymerization temperature to 50°C, and polymerization was carried out for 1 hour. Methanol was then added to stop the polymerization reaction and obtain a polymer solution. Water was added to the obtained polymer solution and stirred, and the polymer solution was washed with water. After stopping the stirring and confirming that the polymer solution phase and the aqueous phase had separated, the water was separated. The polymer solution after washing was vacuum dried at 70°C for 24 hours to obtain unmodified liquid polybutadiene (A'-3). Next, 500 g of the obtained unmodified liquid polybutadiene (A'-3) was charged into a 1 L autoclave that had been purged with nitrogen. 25 g of maleic anhydride and 0.5 g of N-phenyl-N'-(1,3-dimethylbutyl)-p-phenylenediamine (trade name "Nocrac 6C", manufactured by Ouchi Shinko Chemical Industry Co., Ltd.) were added, and the mixture was reacted at 170°C for 24 hours to obtain maleic anhydride-modified liquid polybutadiene (A'-3).

[0099] Manufacturing Example 4: Manufacturing of Modified Conjugated Diene Rubber (A-4) To 525 g of the obtained maleic anhydride-modified liquid polybutadiene (A-3), 9.0 g of methanol was added and the mixture was reacted at 80°C for 6 hours to obtain monomethyl maleic acid-modified liquid polybutadiene (A-4).

[0100] Manufacturing Example 5: Manufacturing of Modified Conjugated Diene Rubber (A-5) To 525 g of the obtained maleic anhydride-modified liquid polybutadiene (A-2), 8.5 g of methanol was added and the mixture was reacted at 80°C for 6 hours to obtain monomethyl maleic acid-modified liquid polybutadiene (A-5).

[0101] The measurement and calculation methods for each physical property of modified conjugated diene rubber are as follows. The results are shown in Table 1. <Methods for measuring weight-average molecular weight, number-average molecular weight, and molecular weight distribution> The weight-average molecular weight (Mw), number-average molecular weight (Mn), and molecular weight distribution (Mw / Mn) of modified conjugated diene rubbers were determined as standard polystyrene equivalents by GPC (gel permeation chromatography). The measurement equipment and conditions are as follows. • Equipment: GPC8020 GPC system manufactured by Tosoh Corporation • Separation column: "TSKgel G4000HXL" manufactured by Tosoh Corporation • Detector: "RI-8020" manufactured by Tosoh Corporation • Eluent: Tetrahydrofuran ·Eluent flow rate: 1.0ml / min • Sample concentration: 5 mg / 10 ml Column temperature: 40℃

[0102] <Method for measuring melt viscosity> The melt viscosity of modified conjugated diene rubber at 38°C was measured using a Brookfield viscometer (manufactured by BROOKFIELD ENGINEERING LABS. INC.).

[0103] <Method for measuring glass transition temperature> Ten mg of modified conjugated diene rubber was placed in an aluminum pan, and a thermogram was measured by differential scanning calorimetry (DSC) at a heating rate of 10°C / min. The peak value of the DSC was defined as the glass transition temperature.

[0104] <Method for measuring vinyl content> The vinyl content of modified conjugated diene rubber is determined by JEOL Ltd. 1 The measurement was performed using 1H-NMR (500 MHz) with a sample / deuterated chloroform concentration of 50 mg / 1 mL and 1024 cumulative measurements. The vinyl content was calculated from the area ratio of the double bond peaks derived from the vinylated diene compound to the double bond peaks derived from the unvinilized diene compound in the obtained spectrum.

[0105] <Average number of hydrogen bonding functional groups per molecule> The average number of hydrogen-bonding functional groups per molecule of modified conjugated diene rubber was calculated from the equivalent amount (g / eq) of hydrogen-bonding functional groups of the modified conjugated diene rubber and the number-average molecular weight Mn in styrene terms using the following formula. Average number of hydrogen-bonding functional groups per molecule = [(number-average molecular weight (Mn)) / (molecular weight of styrene units) × (average molecular weight of conjugated dienes and other monomer units other than conjugated dienes as needed)] / (equivalent weight of hydrogen-bonding functional groups) The method for calculating the equivalent weight of hydrogen-bonding functional groups can be appropriately selected depending on the type of hydrogen-bonding functional group.

[0106] The average number of hydrogen-bonding functional groups per molecule of maleic anhydride-modified conjugated diene rubber and maleic acid monomethyl-modified conjugated diene rubber was calculated by determining the acid value of the maleic anhydride-modified conjugated diene rubber and calculating the equivalent amount (g / eq) of hydrogen-bonding functional groups from the acid value. After the denaturation reaction, the sample was washed four times with methanol (5 mL per 1 g of sample) to remove impurities such as antioxidants, and then the sample was dried under reduced pressure at 80°C for 12 hours. 3 g of the denatured sample was dissolved in 180 mL of toluene and 20 mL of ethanol, and then titrated with a 0.1 N potassium hydroxide solution in ethanol to determine the acid value using the following formula. Acid value (mgKOH / g)=(AB)×F×5.611 / S A: Volume (mL) of ethanol solution of 0.1N potassium hydroxide required for neutralization. B: Droplet volume (mL) of 0.1N potassium hydroxide ethanol solution in a blank without a sample. F: Titer of ethanol solution of 0.1N potassium hydroxide S: Mass of the weighed sample (g)

[0107] From the acid value, the mass of hydrogen-bonding functional groups contained per gram of maleic anhydride-modified conjugated diene rubber and maleic acid monomethyl-modified conjugated diene rubber was calculated using the following formula. Furthermore, the mass of non-functional groups (polymer main chain mass) contained per gram of maleic anhydride-modified conjugated diene rubber and maleic acid monomethyl-modified conjugated diene rubber was calculated. Then, the equivalent weight (g / eq) of hydrogen-bonding functional groups was calculated using the following formula. [Amount of hydrogen-bonding functional groups per gram] = [Acid value] / [56.11] × [Molecular weight of hydrogen-bonding functional groups] / 1000 [Mass of polymer main chain per gram] = 1 - [Mass of hydrogen-bonding functional groups per gram] [Equivalent amount of hydrogen-bonding functional group] = [Mass of polymer main chain per 1g] / ([Mass of hydrogen-bonding functional group per 1g] / [Molecular weight of hydrogen-bonding functional group])

[0108] [Table 1]

[0109] <Constituent materials of the surface modification layer (surface modifier)> The constituent materials for the surface modification layer (surface modifiers B-1 to B-9) were prepared by mixing each component according to the formulations shown in Table 2. [Table 2]

[0110] The details of the compounds listed in Table 2 are as follows: · Blocked isocyanate compounds Meikanate DM-3031 CONC (manufactured by Meisei Chemical Industry Co., Ltd., 54% by mass of pure content) • Epoxy compounds Denacol EX-614B (manufactured by Nagase Chemtec Co., Ltd., 100% pure content by mass) • Compounds containing oxazoline groups Epocross WS-700 (manufactured by Nippon Shokubai Co., Ltd., purity 25% by mass) • Compounds containing a carbodiimide group Carbodilite Prototype (manufactured by Nisshinbo Chemical Co., Ltd., 40% by mass of pure content) • Sodium acrylate compound Aqualic DL-453 (manufactured by Nippon Shokubai Co., Ltd., purity 35% by mass) • Ethylene imine compounds Epomin SP-200 (manufactured by Nippon Shokubai Co., Ltd., 100% pure by mass) • Diamide-type cation compounds Adekamin SF-201 (manufactured by ADEKA Corporation, 80% pure content by mass)

[0111] <Diluted solution of conjugated diene rubber> Solutions of each modified conjugated diene rubber listed in Table 1 were prepared by diluting them to 25% by mass with a fatty acid ester or mineral oil. The fatty acid ester in question is a polyol fatty acid ester (trimethylolpropane tricaprylate), with a vapor pressure of 1.7 × 10⁻⁶ at 20°C. -7A non-volatile substance with a vapor pressure of 7.0 × 10⁻¹⁶ Pa was used. -3 A substance with a Pa rating, a flash point of 158°C, and no volatility was used.

[0112] <Example 1> After immersing PET fibers (total fineness 1100 dtex, single filament fineness 6.10 dtex), which are polyester fibers, in a surface modifier (B-1), the liquid was extracted using a roller. Subsequently, the obtained fibers were dried at 140°C for 60 seconds, and then heat-treated at 240°C for 60 seconds to produce surface-modified fibers. Next, a diluted solution of modified conjugated diene rubber was prepared to have the composition and adhesion amount shown in Table 3. Then, the diluted solution was applied to the surface-modified fibers using an oiling guide and wound up. After that, it was allowed to settle at room temperature (20°C) for 3 days, and then the reinforcing fibers were produced by twisting them at a twist count of 80 T / m.

[0113] <Examples 2-7 and Comparative Examples 1-4> Reinforcement fibers were prepared in the same manner as in Example 1, except that the surface modification layer, adhesive layer, and their adhesion amounts were changed as shown in Table 3.

[0114] <Reference example 1> After immersing PET fibers (total fineness 1100 dtex, single filament fineness 6.10 dtex), which are polyester fibers, in the pretreatment solution described later, the solution was squeezed out with a roller and dried at 140°C for 60 seconds, and then heat-treated at 240°C for 60 seconds. Next, after applying RFL, the yarn was dried at 140°C for 60 seconds, and then heat-treated at 240°C for another 60 seconds to obtain treated yarn. The obtained treated yarn was twisted to produce reinforced fibers with a twist count of 80 T / m. The pretreatment solution and RFL solution used were prepared by the following method.

[0115] [Preparation of RFL pretreatment solution] Water: 96.96 parts by mass Blocked isocyanate: 2.29 parts by mass Epoxy compound: 0.75 parts by mass The pretreatment solution was prepared using blocked isocyanate and epoxy resin. Specifically, "Meikanote DM-3031 CONC" manufactured by Meisei Chemical Industry Co., Ltd. was used as the blocked isocyanate, and "Denacol EX-614B" manufactured by Nagase ChemteX Corporation was used as the epoxy resin.

[0116] [Preparation of RFL solution] A liquid Water: 524 parts by mass Resorcinol: 15 parts by mass Formaldehyde (effective content 37% by mass): 16 parts by mass Sodium hydroxide aqueous solution (effective content 10% by mass): 4 parts by mass The above solution A was aged at a temperature of 25°C for 6 hours.

[0117] B liquid SBR latex (effective content 40% by mass): 207 parts by mass Vinylpyridine-modified SBR latex (effective content 40% by mass): 233 parts by mass After mixing the above-mentioned solution B with the matured solution A, the mixture was aged at 25°C for 16 hours to produce RFL solution.

[0118] <Measuring Zeta Potential> The zeta potential of the fiber surface of the surface-modified fibers obtained in Examples 1-7 and Comparative Examples 1-4 was measured using a flat plate cell with a zeta potential / particle size measurement system ELSZ-1000 (manufactured by Otsuka Electronics Co., Ltd.) at pH=7 and a temperature of 25°C. Specifically, fibers were arranged tightly in a flat plate cell, and a dispersion of monitor particles (polystyrene particles coated with hydroxypropyl cellulose [manufactured by Otsuka Electronics Co., Ltd.]) dispersed in a 10 mM sodium chloride (NaCl) solution was injected into the flat plate cell. Electrophoresis was performed under conditions of an applied voltage of 80 V.

[0119] <Measurement of adhesive strength between reinforcing fibers and EPDM rubber> For the reinforcing fibers obtained in Examples 1-7, Comparative Examples 1-4, and Reference Example 1, evaluation sheets were prepared using the method described below. The force required to peel the reinforcing fibers from the rubber in a T-shape (N / 25.4mm) was measured and evaluated as the rubber adhesion strength. The results are shown in Table 3. The evaluation results for rubber adhesion strength indicate that a higher numerical value indicates greater adhesion between the reinforcing fibers and the rubber. The adhesive sheet was prepared as follows.

[0120] [Creation of evaluation sheet] The reinforcing fibers prepared in the examples, comparative examples, and reference examples were arranged on masking tape in a curtain-like pattern so that the reinforcing fibers did not overlap, and then this was layered with an unvulcanized rubber composition prepared separately using EPDM rubber according to the following compound composition. Next, the temperature was set to 150°C and the pressure to 20 kg / cm². 2 An evaluation sheet was prepared by press-vulcanizing under these conditions for 30 minutes.

[0121] [Composition of unvulcanized EPDM rubber] EPDM rubber: 100 parts by mass Filler (carbon black): 60 parts by mass Softener (paraffin-based process oil): 20 parts by mass Crosslinking agent (sulfur powder): 1.5 parts by mass Vulcanization aids (two types of zinc oxide, stearic acid): 6 parts by mass Vulcanization accelerator (thiazole-based, thiram-based): 1.5 parts by mass

[0122] [Table 3]

[0123] <Examples 8-16 and Comparative Examples 5-9> Reinforcement fibers were prepared in the same manner as in Example 1, except that the fibers, surface modification layer, adhesive layer, and their respective attachment amounts were changed as shown in Table 4. In addition to polyester fibers, polyamide fibers such as nylon fibers (total fineness 1100 dtex, single filament fineness 6.10 dtex) and polyvinyl alcohol fibers such as vinylon fibers (total fineness 1330 dtex, single filament fineness 6.65 dtex, "Kuraron 1239" manufactured by Kuraray Co., Ltd.) were used.

[0124] <Reference example 2> The reinforcing fibers were prepared using the same process as in Reference Example 1, except that no twisting was applied at the end.

[0125] <Measurement of adhesive strength between reinforcing fibers and NR / SBR rubber> For the reinforcing fibers obtained in Examples 8-16, Comparative Examples 5-9, and Reference Example 2, evaluation sheets were prepared using the method described below, and the force (N / 25.4mm) required to peel the reinforcing fibers from the rubber in a T-shape was measured and evaluated as the rubber adhesion strength. The results are shown in Table 4. In the evaluation of rubber adhesion strength, a larger numerical value indicates a greater adhesion strength between the reinforcing fiber and the rubber. The adhesive sheets were prepared as described below.

[0126] [Creation of evaluation sheet] The reinforcing fibers prepared in the aforementioned examples, comparative examples, and reference examples were arranged on masking tape in a curtain-like pattern so that the reinforcing fibers did not overlap, and then this was layered with an unvulcanized rubber composition prepared separately using NR / SBR rubber according to the following compound composition. Next, the temperature was set to 150°C and the pressure to 20 kg / cm². 2 An evaluation sheet was prepared by press-vulcanizing under these conditions for 30 minutes.

[0127] [Formulation composition of NR / SBR unvulcanized rubber] NR rubber: 70 parts by mass SBR rubber: 41.25 parts by mass Filler (carbon black): 45 parts by mass Vulcanizing agent (sulfur powder): 3.5 parts by mass Sulfurization aids (zinc oxide, stearic acid): 6 parts by mass Vulcanization accelerator (thiazole-based): 1 part by mass

[0128] [Table 4]

[0129] <Example 17: Method for processing twisted cords> Two strands of PET polyester fiber (total fineness 1100 dtex, single yarn fineness 6.10 dtex) were twisted 470 times / m on the top and 470 times / m on the bottom to create a twisted fiber cord. The aforementioned twisted cord was immersed in a surface modifier (B-1) and then squeezed with a roller. The resulting fiber cord was dried at 140°C for 60 seconds and then heat-treated at 240°C for 60 seconds to produce the desired product. Next, it was immersed in an emulsion composition mainly composed of the modified conjugated diene rubber described in Table 5, squeezed with a roller, dried at 140°C for 60 seconds, and then wound up. The content of the modified conjugated diene rubber in the emulsion composition was 10% by mass.

[0130] <Examples 18, 19 and Comparative Example 10> Reinforcement fibers were prepared in the same manner as in Example 17, except that the surface modification layer, adhesive layer, and their adhesion amounts were changed as shown in Table 5.

[0131] <Reference example 3> The reinforcing fibers were prepared in the same manner as in Reference Example 1, except that twisted PET fiber cords were used.

[0132] <Measurement of rubber adhesive strength> For the reinforcing fibers obtained in Examples 17-19, Comparative Example 10, and Reference Example 3, evaluation specimens were prepared using the method described below. The force (N / 3 fibers) required to peel the reinforcing fibers from the rubber in a T-shape was measured and evaluated as the rubber adhesion strength. The results are shown in Table 5. In the evaluation of rubber adhesion strength, a larger numerical value indicates a greater adhesion strength between the reinforcing fiber and the rubber. The adhesive specimens were prepared as described below.

[0133] <Preparation of test specimens for evaluation> Three reinforcing fibers prepared in the aforementioned examples, comparative examples, and reference examples were placed at regular intervals in an unvulcanized NR / SBR rubber composition prepared according to the above formulation. Then, the composition was heated to 150°C and pressure of 20 kg / cm². 2 Adhesive specimens were prepared by press-vulcanizing them for 30 minutes under the specified conditions.

[0134] [Table 5]

[0135] As is clear from the results of the examples and comparative examples, the present invention provides surface-modified fibers and reinforcing fibers with excellent adhesion to rubber. In particular, the present invention makes it possible to firmly bond fibers and rubber without using an adhesive mainly composed of resorcinol-formaldehyde resin and rubber latex.

Claims

1. A surface-modified fiber comprising a fiber and a surface-modified layer covering at least a portion of the surface of the fiber, wherein the solid surface zeta potential at the surface of the surface-modified layer is -20.0 to 30.0 mV, and the fiber is a polyvinyl alcohol-based fiber.

2. The surface-modified fiber according to claim 1, wherein the surface-modified layer contains a compound having nitrogen-containing functional groups.

3. The surface-modified fiber according to claim 1 or 2, wherein the surface-modified layer comprises a compound having a functional group selected from one or more of the following: an oxazoline group, an oxazolidinone group, a carbodiimide group, a carbamide group, an amino group, and an aziridine group.

4. The surface-modified fiber according to any one of claims 1 to 3, wherein the amount of the surface-modified layer is 0.01 to 5.0 parts by mass per 100 parts by mass of fiber used as raw material.

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