JP7189381B2 - V-belt for power transmission - Google Patents

Description

TECHNICAL FIELD The present invention relates to a transmission V-belt containing a cured rubber composition containing an ethylene-α-olefin elastomer.

V-belts that transmit power by frictional transmission include a raw-edge type (raw-edge V-belt), which is a rubber layer with an exposed frictional transmission surface (V-shaped side surface), and a frictional transmission surface (V-shaped side surface). ) is covered with a cover cloth (wrapped V-belt), which is used according to the application due to the difference in the surface properties of the friction transmission surface (coefficient of friction between the rubber layer and the cover cloth). . Raw edge type belts include low edge V belts without cogs, low edge cogged V belts with cogs only on the lower surface (inner peripheral surface) of the belt to improve flexibility, and lower surface (inner peripheral surface) of the belt. There is a low-edge cogged V-belt (low-edge double cogged V-belt) in which cogs are provided on both the outer surface (peripheral surface) and the upper surface (peripheral surface) to improve flexibility.

These V-belts are used in a wide range of fields such as automobiles and industrial machinery. Among them, V-belts used in belt-type transmissions mounted on motorcycles, snowmobiles, large agricultural machines, etc. are called speed change belts.

V-belts are used under heavy loads due to increased power transmission capacity, increased device size, and increased horsepower. Therefore, in order to prevent buckling deformation (dishing), the V-belt is required to have increased rigidity in the belt width direction (lateral pressure resistance).

In particular, transmission belts are required to have a high degree of lateral pressure resistance so as to withstand severe movements in sliding with pulleys. For example, the sizes of large V-belts used in power transmission mechanisms (particularly belt-type transmissions) of the largest agricultural machinery are HL to HQ (ISO3410 : name described in 1989), which has a belt width (upper width) of 44.5 to 76.2 mm and a belt thickness of 19.8 to 30.5 mm. There is also a non-standard product with a thickness of 36 mm. In such large agricultural machines, it is necessary to apply a very high tension to the V-belt in order to transmit a huge load, and accordingly the V-belt receives a very high lateral pressure from the pulleys.

Furthermore, the speed change belt is cold at the time of start-up, but is exposed to the heat generated by the engine and becomes hot at the time of drive. Therefore, a rubber composition that can withstand a wide temperature range from low to high is required. In addition, the speed change belt has high adhesiveness to suppress separation between the rubber composition and fiber members such as cords and reinforcing fabrics, and stress concentration on the cog valley due to repeated winding and release on the pulley. Endurable bending fatigue resistance is required. Furthermore, a high degree of wear resistance that can withstand wear due to contact with pulleys is also required. It is very difficult to meet these demands with conventional large V-belts.

As described above, in order to meet various demands for transmission V-belts, transmission V-belts using various rubber compositions containing chloroprene rubber and ethylene-α-olefin elastomer as polymer components have been proposed.

For example, Japanese Patent Laying-Open No. 2012-241831 (Patent Document 1) discloses a power transmission belt in which a compressed rubber layer includes a fatty acid amide and short fibers. Examples of rubber components include chloroprene rubber and ethylene-α-olefin elastomers, and examples of vulcanizing agents or cross-linking agents include metal oxides, organic peroxides, and sulfur-based vulcanizing agents. Further, in the examples, a low-edge cogged V-belt is produced using a rubber composition containing chloroprene rubber and sulfur. Then, an example (Example 7) in which the hardness of the rubber composition is 94 ° and the breaking elongation in the direction perpendicular to the short fibers is 70%, and the hardness of the rubber composition is 86 to 88 ° and the breaking elongation in the direction perpendicular to the short fibers Examples (Examples 1 to 6) having an elongation of 180 to 245% are described.

Further, in Japanese Patent Application Laid-Open No. 2009-52740 (Patent Document 2), a compression rubber layer is formed by adding polyparaphenylenebenzobisoxazole to 100 parts by mass of ethylene/α-olefin rubber having an ethylene content of 40 to 70% by mass. Composed of an organic peroxide-based crosslinked product of a rubber composition containing 5 to 40 parts by mass of (PBO) short fibers and containing 5 to 50 parts by mass of short fibers, the compressed rubber layer has a belt longitudinal breaking elongation of 70. % or more. The breaking elongation in the longitudinal direction of the belt is preferably 70% or more, more preferably 200% or more, and it is said that having such physical properties makes it difficult for the belt to crack, and the belt can have a longer life. Have been described. In addition, the hardness (JIS-A) of the crosslinked rubber composition may be in the range of 85 to 93, and by setting the JIS-A hardness to 85 or more, combined with the addition of PBO short fibers, the belt can be used. It is described that the abrasion resistance can be greatly improved, and that if the hardness (JIS-A) exceeds 93, the belt becomes too hard and cracks easily occur due to repeated bending of the belt, which is not preferable. In this document, it is essential that the cross-linking agent be an organic peroxide, and an example of cross-linking with sulfur is described as a comparative example.

Further, Japanese Patent Application Laid-Open No. 2018-141554 (Patent Document 3) describes a rubber component containing an ethylene-α-olefin elastomer, an α,β-unsaturated carboxylic acid metal salt, magnesium oxide, and an organic peroxide. , an inorganic filler, and a cured product of a rubber composition, wherein the ratio of the magnesium oxide is 2 to 20 parts by mass with respect to 100 parts by mass of the rubber component, and the α, β - A transmission belt is disclosed in which the unsaturated carboxylic acid metal salt is 5 parts by mass or more per 100 parts by mass. With such a configuration, it is possible to increase the hardness and modulus of the cured product of the transmission belt rubber composition without impairing cold resistance, heat resistance, adhesiveness, bending fatigue resistance, and wear resistance. Have been described. It also describes that the cured rubber composition may have a rubber hardness (JIS-A) of 90 to 100 degrees. Also in this document, the cross-linking agent must be an organic peroxide, and cross-linking with sulfur is not taken into consideration.

JP 2012-241831 A JP-A-2009-52740 JP 2018-141554 A

As is clear from Patent Documents 1 to 3, conventionally, chloroprene rubbers are generally crosslinked with sulfur, and ethylene-α-olefin elastomers are generally crosslinked with organic peroxides. The reason for this is that chloroprene rubber having double bonds in its main chain is easily crosslinked by sulfur, and the cured product obtained by sulfur crosslinking exhibits excellent physical properties. On the other hand, ethylene-α-olefin elastomers having no double bond in the main chain are not effectively crosslinked by sulfur, and physical properties of cured products are not sufficiently improved. Although organic peroxides are effective in improving the physical properties of cured ethylene-α-olefin elastomers, ethylene-α-olefin elastomers crosslinked with organic peroxides tend to be brittle. When applied to belts, there is a problem that cracks are likely to occur, and an improvement has been desired. In particular, as in the configuration disclosed in Patent Document 3, when the hardness and modulus are increased by the α,β-unsaturated carboxylic acid metal salt and magnesium oxide, the occurrence of cracks is promoted. It has been difficult to sufficiently improve the life of the V-belt for industrial use.

Accordingly, an object of the present invention is to provide a power transmission V-belt containing a cured rubber composition containing an ethylene-α-olefin elastomer as a polymer component with lateral pressure resistance, abrasion resistance, and adhesion to fiber members such as short fibers. The purpose of the present invention is to improve the bending fatigue resistance of the belt while ensuring the durability, suppress the generation of cracks, and improve the life of the belt.

As a result of intensive studies to achieve the above object, the present inventors have found that a polymer component (A) containing an ethylene-α-olefin elastomer, a cross-linking agent (B) containing a sulfur-based cross-linking agent, and short fibers (C) By adjusting the rubber hardness and elongation at break of the cured product of the rubber composition in which the short fibers (C) are oriented in the belt width direction, lateral pressure resistance, abrasion resistance, short fibers, etc. The present inventors have found that it is possible to provide a power transmission V-belt that can improve the bending fatigue resistance and suppress the occurrence of cracks while ensuring the adhesion to the fiber member of the belt and improve the belt life, and completed the present invention.

That is, the power transmission V-belt of the present invention is a power transmission V-belt containing a cured product of a first rubber composition, wherein the first rubber composition is a polymer component containing an ethylene-α-olefin elastomer ( A), a cross-linking agent (B) containing a sulfur-based cross-linking agent, and short fibers (C), wherein the short fibers (C) are oriented in the belt width direction, and the rubber hardness of the cured product (JIS-A) is 91 degrees or more, and the breaking elongation of the cured product in the longitudinal direction of the belt is 100% or more. In the transmission V-belt, a cured rubber composition obtained by removing the short fibers (C) from the rubber composition may have a matrix rubber hardness (JIS-A) of 83 degrees or more. The first rubber composition may further contain a cross-linking accelerator (D). The cross-linking accelerator (D) may contain a sulfur-containing cross-linking accelerator. The sulfur-containing cross-linking accelerator may comprise a sulfur-containing cross-linking accelerator having an oxygen- and nitrogen-containing heterocycle. The first rubber composition may further contain a co-crosslinking agent (E). The co-crosslinking agent (E) may contain a bismaleimide compound. The first rubber composition may further contain an adhesion improver (F). The ratio of the sulfur-based cross-linking agent may be 1.2 parts by mass or more with respect to 100 parts by mass of the polymer component (A). The first rubber composition may further contain a softening agent (G). A ratio of the softening agent (G) may be 0.1 to 10 parts by mass with respect to 100 parts by mass of the polymer component (A). The transmission V-belt may include a compression rubber layer and/or a stretch rubber layer formed of a cured product of the first rubber composition. The transmission V-belt may further include an adhesive rubber layer formed of a cured product of a second rubber composition, the second rubber composition being a polymer component containing an ethylene-α-olefin elastomer. (a) and a cross-linking agent (b) comprising a sulfur-based cross-linking agent may be included. The transmission V-belt may be a raw edge cogged V-belt having cogs on at least the inner peripheral surface side. The transmission V-belt may be a variable speed belt. An average thickness of the entire belt of the transmission V-belt may be 19.8 to 36 mm. The transmission V-belt may be a raw edge type V-belt used in a layout including reverse bending.

The power transmission V-belt of the present invention combines a polymer component (A) containing an ethylene-α-olefin elastomer, a cross-linking agent (B) containing a sulfur-based cross-linking agent, and short fibers (C), and the short fibers (C ) is oriented in the belt width direction, and the hardness and elongation at break of the cured product are adjusted to specific ranges. Therefore, while securing lateral pressure resistance, abrasion resistance, and adhesiveness to fibrous members such as short fibers, the bending fatigue resistance can be enhanced to suppress the occurrence of cracks, and the belt life can be improved. In particular, since the power transmission V-belt of the present invention is excellent in resistance to bending fatigue, even when used in a layout including so-called "reverse bending" in which the back side of the power transmission V-belt is bent inward. can also effectively prevent the occurrence of cracks. Furthermore, transmission belts for large agricultural machines that are thick and require high horsepower require high lateral pressure resistance and bending fatigue resistance, and the power transmission V-belt of the present invention has high durability. It can be used to improve belt life. Therefore, the power transmission V-belt of the present invention is suitable for use as a speed change belt, and most suitable for use as a speed change belt for large agricultural machinery.

FIG. 1 is a schematic partial cross-sectional perspective view showing an example of the power transmission V-belt (low edge cogged V-belt) of the present invention. FIG. 2 is a schematic cross-sectional view of the transmission V-belt of FIG. 1 cut in the longitudinal direction of the belt. FIG. 3 is a schematic perspective view for explaining the method of measuring the 8% bending stress of the crosslinked rubber moldings obtained in the examples. FIG. 4 is a schematic perspective view of a double-cogged V-belt manufactured in Examples. FIG. 5 is a schematic diagram showing the layout of a biaxial endurance running test of the transmission V-belt obtained in the example. FIG. 6 is a schematic diagram showing the layout of the reverse bending endurance running test of the transmission V-belt obtained in the example. FIG. 7 is a schematic diagram for explaining the measuring method of the reverse bending crack test of the power transmission V-belt obtained in the example.

[Rubber composition]
The power transmission V-belt of the present invention is a rubber composition (a first rubber composition) including cured products.

(A) Polymer Component The polymer component (A) contains an ethylene-α-olefin elastomer (first ethylene-α-olefin elastomer) because of its excellent cold resistance, heat resistance and weather resistance.

The ethylene-α-olefin elastomer may contain ethylene units and α-olefin units as structural units, and may further contain diene units. Therefore, ethylene-α-olefin elastomers include ethylene-α-olefin copolymer rubbers, ethylene-α-olefin-diene terpolymer rubbers, and the like.

Examples of α-olefins for forming α-olefin units include linear α-C _3-12 olefins such as propylene, butene, pentene, methylpentene, hexene and octene. Of these α-olefins, α-C _3-4 olefins such as propylene (particularly propylene) are preferred.

A non-conjugated diene monomer is usually used as the diene monomer for forming the diene unit. Examples of non-conjugated diene monomers include dicyclopentadiene, methylenenorbornene, ethylidenenorbornene, 1,4-hexadiene, and cyclooctadiene. Among these diene monomers, ethylidenenorbornene and 1,4-hexadiene (especially ethylidenenorbornene) are preferred.

Typical ethylene-α-olefin elastomers include, for example, ethylene-α-olefin rubber [ethylene-propylene rubber (EPM), ethylene-butene rubber (EBM), ethylene-octene rubber (EOM), etc.], ethylene-α-olefin -Diene rubber [ethylene-propylene-diene terpolymer (EPDM)] and the like can be exemplified.

These ethylene-α-olefin elastomers can be used alone or in combination of two or more. Among these, ethylene-α-olefin-diene terpolymer rubber such as ethylene-α-C _3-4 olefin-diene terpolymer rubber is preferred because of its excellent cold resistance, heat resistance and weather resistance. EPDM is particularly preferred. Therefore, the proportion of EPDM may be 50% by mass or more, preferably 80% by mass or more, more preferably 90% by mass or more (especially 95% by mass or more), relative to the entire ethylene-α-olefin elastomer, It may be 100% by mass (only EPDM).

In the ethylene-α-olefin elastomer, the ratio (mass ratio) between ethylene and α-olefin is the former/latter = 40/60 to 90/10, preferably 45/55 to 85/15 (for example, 50/50 to 80 /20), more preferably 52/48 to 70/30. In particular, in the ethylene-propylene-diene terpolymer, the ratio (mass ratio) of ethylene and propylene is the former/latter=35/65 to 90/10, preferably 40/60 to 80/20, more preferably may be from 45/55 to 70/30, most preferably from 50/50 to 60/40.

The diene content of the ethylene-α-olefin elastomer (especially ethylene-α-olefin-diene terpolymer rubber such as EPDM) may be 15% by mass or less (for example, 0.1 to 15% by mass), Preferably 10% by mass or less (eg 0.3 to 10% by mass), more preferably 5% by mass or less (eg 0.5 to 5% by mass), more preferably 4% by mass or less (eg 1 to 4% by mass) , and most preferably 3% by mass or less (eg, 1 to 3% by mass). If the diene content is too high, there is a risk that high heat resistance cannot be ensured.

In the present application, the diene content means the mass ratio of diene monomer units in all units constituting the ethylene-α-olefin elastomer, and can be measured by a conventional method, but may be a ratio based on monomers.

The iodine value of the ethylene-α-olefin elastomer containing diene units is, for example, 3-40, preferably 5-30, more preferably 10-20. If the iodine value is too small, the cross-linking of the rubber composition is insufficient and wear and adhesion tend to occur. tends to decrease.

In addition, in the present application, the iodine value of the ethylene-α-olefin elastomer can be measured by a conventional method, for example, by infrared spectroscopy.

Mooney viscosity [ML (1+4) 125° C.] of the uncrosslinked ethylene-α-olefin elastomer may be 80 or less, for example 10 to 80, preferably 20 to 70, more preferably 30 to 50, most preferably 35-45. If the Mooney viscosity is too high, the fluidity of the rubber composition may be lowered and the workability in kneading may be lowered.

In the present application, the Mooney viscosity can be measured by a method according to JIS K 6300-1 (2013), and the test conditions are an L-shaped rotor, a test temperature of 125°C, a preheat of 1 minute, and a rotor operating time of 4 minutes. is.

The proportion of the ethylene-α-olefin elastomer in the polymer component (A) may be 50% by mass or more, preferably 80% by mass or more, more preferably 90% by mass or more, and most preferably 100% by mass (ethylene -α-olefin elastomers only). If the proportion of the ethylene-α-olefin elastomer in the polymer component is too low, the heat resistance and cold resistance may deteriorate.

In addition to the ethylene-α-olefin elastomer, the polymer component (A) includes other rubber components, such as diene rubbers [e.g., natural rubber, isoprene rubber, butadiene rubber, , chloroprene rubber, styrene-butadiene rubber (SBR), vinylpyridine-styrene-butadiene copolymer rubber, acrylonitrile-butadiene rubber (nitrile rubber); hydrogenated nitrile rubber (mixed polymer of hydrogenated nitrile rubber and unsaturated carboxylic acid metal salt hydrogenated products of diene rubbers, etc.], olefin rubbers (e.g., polyoctenylene rubber, ethylene-vinyl acetate copolymer rubber, chlorosulfonated polyethylene rubber, alkylated chlorosulfonated polyethylene rubber, etc. ), epichlorohydrin rubber, acrylic rubber, silicone rubber, urethane rubber, fluorine rubber, and the like.

The proportion of other rubber components in the polymer component (A) may be 50% by mass or less, preferably 20% by mass or less, and more preferably 10% by mass or less.

(B) Cross-linking agent (vulcanizing agent)
The cross-linking agent (B) contains a sulfur-based cross-linking agent (first sulfur-based cross-linking agent). In conventional well-known techniques, an organic peroxide is used as a cross-linking agent for an ethylene-α-olefin elastomer. The bending fatigue resistance (crack resistance) of the cured product can be improved.

Examples of sulfur-based cross-linking agents include powdered sulfur, precipitated sulfur, colloidal sulfur, insoluble sulfur, highly dispersible sulfur, sulfur chloride (sulfur monochloride, sulfur dichloride, etc.), and the like. These sulfur-based cross-linking agents can be used alone or in combination of two or more. Among these, powdered sulfur, precipitated sulfur, colloidal sulfur, insoluble sulfur, and highly dispersible sulfur are preferred, and powdered sulfur is particularly preferred.

The ratio of the sulfur-based cross-linking agent can be selected, for example, from a range of about 1 to 10 parts by mass, preferably 1.2 parts by mass or more, for example, 1.2 to 5 parts by mass, with respect to 100 parts by mass of the polymer component (A). , preferably 1.3 to 3 parts by mass, more preferably 1.5 to 2.5 parts by mass, more preferably 1.6 to 2.3 parts by mass, most preferably 1.8 to 2.2 parts by mass be. If the proportion of the sulfur-based cross-linking agent is too low, rubber hardness, lateral pressure resistance, and wear resistance may decrease. precipitation) may occur.

The cross-linking agent (B) may further contain an organic peroxide as another cross-linking agent (or vulcanizing agent). Examples of organic peroxides include organic peroxides commonly used for cross-linking rubbers and resins, such as diacyl peroxide, peroxy ester, dialkyl peroxide (e.g., dicumyl peroxide, t-butyl cumyl peroxide, oxide, 1,1-di-butylperoxy-3,3,5-trimethylcyclohexane, 2,5-dimethyl-2,5-di(t-butylperoxy)-hexane, 1,3-bis(t- butylperoxy-isopropyl)benzene, di-t-butylperoxide, etc.). These organic peroxides can be used alone or in combination of two or more. Furthermore, the organic peroxide is preferably a peroxide having a decomposition temperature of about 150 to 250° C. (eg, 175 to 225° C.), which gives a half-life of 1 minute by thermal decomposition.

The proportion of the organic peroxide may be 100 parts by mass or less, preferably 50 parts by mass or less, more preferably 30 parts by mass or less, and more preferably 10 parts by mass or less with respect to 100 parts by mass of the sulfur-based cross-linking agent. is. If the proportion of the organic peroxide is too high, the bending fatigue resistance of the cured product may deteriorate. It is particularly preferred that the cross-linking agent (B) is substantially free of organic peroxides, most preferably free of organic peroxides.

The proportion of the sulfur-based cross-linking agent in the cross-linking agent (B) may be 50% by mass or more, preferably 70% by mass or more, more preferably 90% by mass or more, and more preferably 100% by mass. If the proportion of the sulfur-based cross-linking agent is too low, the bending fatigue resistance of the cured product may be lowered.

The ratio of the cross-linking agent (B) can be selected, for example, from a range of about 1 to 10 parts by mass, for example, 1.2 to 10 parts by mass, preferably 1.3 to 8 parts by mass, with respect to 100 parts by mass of the polymer component (A). parts by mass, more preferably 1.5 to 5 parts by mass, more preferably 1.6 to 3 parts by mass, and most preferably 1.8 to 2.5 parts by mass.

(C) Staple fibers Staple fibers (C) include, for example, polyolefin fibers (polyethylene fibers, polypropylene fibers, etc.), polyamide fibers (e.g., aliphatic polyamide fibers such as polyamide 6 fibers, polyamide 66 fibers, and polyamide 46 fibers; aramid fiber, etc.), polyalkylene arylate-based fiber [e.g., polyethylene terephthalate (PET) fiber, polyethylene naphthalate (PEN) fiber, etc., poly C _2-4 alkylene C _6-14 arylate-based fiber], vinylon fiber, polyvinyl alcohol Synthetic fibers such as synthetic fibers and polyparaphenylenebenzobisoxazole (PBO) fibers; natural fibers such as cotton, hemp, and wool; and inorganic fibers such as carbon fibers.

These short fibers can be used alone or in combination of two or more. Among these short fibers, synthetic fibers (e.g., polyamide fibers, polyalkylene arylate fibers, etc.) are commonly used, and polyamide fibers are preferable. Short fibers containing fibers are more preferable, and a combination of aramid fibers and aliphatic polyamide fibers is more preferable from the viewpoint of excellent balance of properties. Aramid fibers are commercially available, for example, under the trade names "Conex", "Nomex", "Kevlar", "Technora", "Twaron" and the like.

When the short fibers are a combination of aramid fibers and aliphatic polyamide fibers, the proportion of the aliphatic polyamide fibers may be 100 parts by mass or less with respect to 100 parts by mass of the aramid fibers, for example 1 to 100 parts by mass, It is preferably 5 to 80 parts by mass, more preferably 10 to 70 parts by mass, and more preferably 30 to 60 parts by mass. If the ratio of the aliphatic polyamide fibers is too high, there is a possibility that the rigidity of the cured product may be lowered.

The staple fiber (C) has an average fineness of, for example, 0.1 to 50 dtex, preferably 1 to 10 dtex, more preferably 1.5 to 5 dtex, and more preferably 2 to 3 dtex. If the average fineness is too large, the mechanical properties of the cured product of the rubber composition may deteriorate, and if it is too small, it may be difficult to uniformly disperse the fine particles.

The short fibers (C) have an average length of, for example, 1 to 20 mm, preferably 1.2 to 15 mm (eg, 1.5 to 10 mm), more preferably 2 to 5 mm, more preferably 2.5 to 4 mm. If the average length of the short fibers is too short, the mechanical properties (for example, modulus) in the orientation direction (grain direction) of the short fibers may not be sufficiently enhanced. There is a possibility that the dispersibility of the short fibers in the fiber may decrease, and the bending fatigue resistance may decrease.

From the standpoint of dispersibility and adhesiveness of the short fibers in the rubber composition, at least the short fibers are preferably subjected to adhesion treatment (or surface treatment). Note that not all the staple fibers need to be adhesively treated, and adhesively treated staple fibers and non-adhesively treated staple fibers (untreated staple fibers) may be mixed or used together.

In the adhesive treatment of the short fibers (C), various adhesive treatments, for example, a treatment liquid containing an initial condensate of phenols and formalin (novolac or resol type phenolic resin prepolymer, etc.), a rubber component (or latex) are used. treatment liquid, treatment liquid containing the initial condensate and rubber component (latex), treatment liquid containing reactive compounds (adhesive compounds) such as silane coupling agents, epoxy compounds (epoxy resins, etc.), isocyanate compounds, etc. can be processed with In a preferred bonding treatment, the short fibers are treated with a treatment liquid containing said precondensate and a rubber component (latex), especially at least a resorcin-formalin-latex (RFL) liquid. Such treatment liquids may be used in combination, for example, short fibers may be pretreated with a conventional adhesive component, e.g. After treatment, it may be treated with an RFL solution.

The ratio of the short fibers (C) is, for example, 5 to 100 parts by mass, preferably 10 to 50 parts by mass, more preferably 20 to 40 parts by mass, and more preferably 25 to 100 parts by mass with respect to 100 parts by mass of the polymer component (A). 35 parts by mass. If the ratio of the short fibers is too low, the mechanical properties of the cured rubber composition may deteriorate. There is

In the present invention, the short fibers (C) are oriented in the belt width direction, and the grain direction of the short fibers (C) is in the belt width direction, so that the hardness and rigidity of the polymer component (A) can be improved. , the lateral pressure resistance of the belt can be improved.

In the present application, the "grain direction" may be not only the longitudinal direction of the short fibers, but also a direction within a range of ±5° in the longitudinal direction. Therefore, the "grain direction" can also be said to be "a direction substantially parallel to the longitudinal direction of the staple fibers", and "the grain direction is substantially parallel to the belt width direction" and "the grain direction is substantially parallel to the belt width direction". It can also be said that there is

(D) Crosslinking accelerator The rubber composition may further contain a crosslinking accelerator (D). In addition, the cross-linking accelerator (D) preferably contains a sulfur-containing cross-linking accelerator (first sulfur-containing cross-linking accelerator) because the cross-linking accelerator is highly effective in combination with a sulfur-based cross-linking agent.

Examples of sulfur-containing crosslinking accelerators include thiuram-based accelerators [e.g., tetramethylthiuram monosulfide (TMTM), tetramethylthiuram disulfide (TMTD), tetraethylthiuram disulfide (TETD), tetrabutylthiuram disulfide ( TBTD), dipentamethylenethiuram tetrasulfide (DPTT), etc.], sulfenamide accelerators [e.g., N-cyclohexyl-2-benzothiazylsulfenamide (CBS), Nt-butyl-2-benzothia disulfenamide (TBBS), etc.], thiomorpholine accelerators [e.g., 4,4'-dithiodimorpholine (DTDM), 2-(4'-morpholinodithio)benzothiazole, etc.], thiazole accelerators [For example, 2-mercaptobenzothiazole (MBT), zinc salt of MBT, 2-mercaptobenzothiazole dibenzothiazyl disulfide (MBTS), etc.], thiourea-based accelerators [for example, ethylenethiourea, trimethylthiourea (TMU ), diethylthiourea (EDE), etc.], dithiocarbamate accelerators [e.g., sodium dimethyldithiocarbamate, zinc diethyldithiocarbamate (EZ), zinc dibutyldithiocarbamate (BZ), etc.], xanthate accelerators (isopropylxanthogen zinc acid, etc.), etc.).

These sulfur-containing cross-linking accelerators can be used alone or in combination of two or more. Among these sulfur-based cross-linking accelerators, sulfur-containing cross-linking accelerators having an oxygen- and nitrogen-containing heterocyclic ring such as oxazole, furazane, and morpholine (particularly , thiomorpholine-based accelerators) are preferred.

Sulfur-containing accelerators, including sulfur-containing accelerators with oxygen- and nitrogen-containing heterocycles, include sulfur-containing accelerators with oxygen- and nitrogen-containing heterocycles (especially thiomorpholine-based accelerators) and other sulfur-containing accelerators. A combination with a cross-linking accelerator (especially a thiuram-based accelerator and/or a sulfenamide-based accelerator) may be used, and the mass ratio of the two is from 99/1 to 10/90, preferably 95. /5 to 20/80, more preferably 90/10 to 30/70, more preferably 80/20 to 50/50, most preferably 70/30 to 60/40.

The cross-linking accelerator (D) may further contain a sulfur-free cross-linking accelerator in addition to the sulfur-containing cross-linking accelerator.

Examples of sulfur-free cross-linking accelerators include guanidine-based accelerators [e.g., diphenylguanidine (DPG), diorthotolylguanidine (DOTG), etc.], aldehyde-amine-based or aldehyde-ammonia-based accelerators [e.g., hexanemethylenetetramine etc.] and the like.

The proportion of the sulfur-free cross-linking accelerator may be 100 parts by mass or less, preferably 50 parts by mass or less, more preferably 30 parts by mass or less, more preferably 10 parts by mass or less per 100 parts by mass of the sulfur-containing cross-linking accelerator. Part by mass or less. If the ratio of the sulfur-free cross-linking accelerator is too high, the scorch-suppressing effect may be lowered.

The ratio of the sulfur-containing cross-linking accelerator in the cross-linking accelerator (D) may be 50% by mass or more, preferably 70% by mass or more, more preferably 90% by mass or more, and more preferably 100% by mass. If the ratio of the sulfur-containing cross-linking accelerator is too small, the scorch-suppressing effect may be lowered.

The ratio of the cross-linking accelerator (D) can be selected from a range of, for example, about 0.1 to 10 parts by mass, for example, 0.5 to 8 parts by mass, preferably 1 to 10 parts by mass, relative to 100 parts by mass of the polymer component (A). 7 parts by mass, more preferably 1.5 to 5 parts by mass, more preferably 2 to 4 parts by mass, most preferably 2.5 to 3.5 parts by mass.

The ratio of the sulfur-containing cross-linking accelerator having an oxygen- and nitrogen-containing heterocyclic ring is, for example, 0.1 to 5 parts by mass, preferably 0.3 to 4 parts by mass, more preferably 0.3 to 4 parts by mass, with respect to 100 parts by mass of the polymer component (A). is 0.5 to 3 parts by weight, more preferably 1 to 2.5 parts by weight, most preferably 1.5 to 2 parts by weight.

(E) Co-crosslinking agent (crosslinking aid)
The rubber composition may further contain a co-crosslinking agent (E). Moreover, the co-crosslinking agent (E) preferably contains a bismaleimide compound from the viewpoint of improving lateral pressure resistance and wear resistance.

Examples of bismaleimide compounds include aliphatic bismaleimides (eg, N,N'-1,2-ethylenedimaleimide, 1,6'-bismaleimide-(2,2,4-trimethyl)cyclohexane, etc.), aromatic group bismaleimide {e.g. N,N'-m-phenylenedimaleimide, 4-methyl-1,3-phenylenedimaleimide, 4,4'-diphenylmethanedimaleimide, 2,2-bis[4-(4-maleimide phenoxy)phenyl]propane, 4,4′-diphenyletherdimaleimide, 4,4′-diphenylsulfonedimaleimide, 1,3-bis(3-maleimidophenoxy)benzene, etc.)} and the like.

These bismaleimide compounds can be used alone or in combination of two or more. Among these, aromatic bismaleimides (arene bismaleimides) such as N,N'-m-phenylene dimaleimide are preferred from the viewpoint of excellent heat resistance.

The co-crosslinking agent (E) may further contain other co-crosslinking agents in addition to the bismaleimide compound.

Other co-crosslinking agents include, for example, polyfunctional (iso)cyanurate [e.g., triallyl isocyanurate (TAIC), triallyl cyanurate (TAC), etc.], polydiene (e.g., 1,2-polybutadiene, etc.), α , β-unsaturated carboxylic acid metal salts [e.g., zinc (meth)acrylate, magnesium (meth)acrylate, etc.], oximes (e.g., quinonedioxime, etc.), guanidines (e.g., diphenylguanidine, etc.), polyfunctional (meth)acrylates [eg, ethylene glycol di(meth)acrylate, butanediol di(meth)acrylate, trimethylolpropane tri(meth)acrylate] and the like.

The proportion of the other co-crosslinking agent may be 100 parts by mass or less, preferably 50 parts by mass or less, more preferably 30 parts by mass or less, and more preferably 10 parts by mass or less with respect to 100 parts by mass of the bismaleimide compound. is. If the ratio of the other co-crosslinking agent is too high, the effect of improving lateral pressure resistance and wear resistance may decrease. The co-crosslinking agent (E), among other co-crosslinking agents, substantially contains a metal salt of an α,β-unsaturated carboxylic acid such as zinc (meth)acrylate because it can improve bending fatigue resistance. It is particularly preferred to be free of metal salts of α,β-unsaturated carboxylic acids.

The proportion of the bismaleimide compound in the co-crosslinking agent (E) may be 50% by mass or more, preferably 70% by mass or more, more preferably 90% by mass or more, and more preferably 100% by mass. If the ratio of the bismaleimide compound is too small, the effect of improving lateral pressure resistance and wear resistance may decrease.

The proportion of the co-crosslinking agent (E) can be selected, for example, from a range of about 0.1 to 10 parts by mass, for example, 0.3 to 8 parts by mass, preferably 0.1 part by mass, based on 100 parts by mass of the polymer component (A). 5 to 5 parts by mass, more preferably 0.8 to 4 parts by mass, more preferably 1 to 3 parts by mass, and most preferably 1.5 to 2.5 parts by mass. If the proportion of the co-crosslinking agent (E) is too small, the abrasion resistance may be lowered, and if it is too large, the bending fatigue resistance may be lowered.

(F) Adhesion Improving Agent The rubber composition can improve the adhesion between the polymer component (A) and the fiber member (the short fiber (C), the core body described later, the reinforcing cloth, etc.). A improver (F) may be further included.

Adhesion improvers (F) include, for example, resorcinol-formaldehyde resins (condensates of resorcinol and formaldehyde), amino resins [condensates of nitrogen-containing cyclic compounds and formaldehyde, such as hexamethylolmelamine, hexaalkoxymethylmelamine melamine resins such as (hexamethoxymethyl melamine, hexabutoxymethyl melamine, etc.), urea resins such as methylol urea, benzoguanamine resins such as methylol benzoguanamine resin, etc.], co-condensates thereof (resorcin-melamine-formaldehyde co-condensates, etc.) etc. Resorcinol-formaldehyde resins, amino resins and said co-condensates may be initial condensates (prepolymers) of formaldehyde and nitrogen-containing cyclic compounds such as resorcin and/or melamine.

These adhesion improvers (F) can be used alone or in combination of two or more. Among these, resorcinol-formaldehyde resins and melamine resins are preferred, and resorcinol-formaldehyde resins are particularly preferred.

The proportion of the adhesion improver (F) can be selected from a range of, for example, about 0.1 to 10 parts by weight, for example, 0.3 to 8 parts by weight, preferably 0, per 100 parts by weight of the polymer component (A). 0.5 to 5 parts by weight, more preferably 0.8 to 4 parts by weight, more preferably 1 to 3 parts by weight, and most preferably 1.5 to 2.5 parts by weight.

(G) Softeners (oils)
The rubber composition may further contain a softening agent (G) as an oil (oil component) in order to improve bending fatigue resistance. Softeners (G) may be so-called plasticizers.

Examples of softening agents (G) include mineral oil softening agents {e.g., petroleum softening agents [paraffin oils, alicyclic oils (naphthenic oils), aromatic oils, etc.], coal tar softening agents. [coal tar, cumarone-indene resin, etc.], etc.}, vegetable oil-based softening agents {e.g., fatty oil-based softening agents [fatty acids such as stearic acid and stearic acid metal salts or metal salts thereof; fatty acid esters such as stearic acid esters; Fatty acid amides such as acid amides; fatty oils, etc.]; pine tree-derived softeners [pine tar, rosin, sub (factice), etc.], etc.}, synthetic softeners {e.g., synthetic resin softeners [hydrocarbon synthetic oils (low molecular weight paraffin, low molecular weight wax, phenol-aldehyde resin, liquid ethylene-α-olefin copolymer, etc.), liquid rubber (liquid polybutene, liquid polybutadiene, liquid isoprene rubber, etc.)], synthetic plasticizers (dioctyl phthalate, etc.) acid diesters, polyester plasticizers, C _6-18 alkanedicarboxylic acid esters such as dioctyl sebacate, etc.), etc.).

These softening agents (G) can be used alone or in combination of two or more. Among these, petroleum softeners such as paraffin oils and C _8-24 fatty acids such as stearic acid (including metal salts, esters and _amides thereof) are preferred. are particularly preferred.

When the softener (G) is a combination of a petroleum-based softener and a C _8-24 fatty acid, the proportion of the C _8-24 fatty acid is, for example, 1 to 100 parts by mass with respect to 100 parts by mass of the petroleum-based softener. parts, preferably 3 to 80 parts by mass, more preferably 5 to 50 parts by mass, more preferably 10 to 30 parts by mass.

The ratio of the softening agent (G) is 10 parts by mass or less (for example, 0.1 to 10 parts by mass, particularly 5 parts by mass) with respect to 100 parts by mass of the polymer component (A) from the viewpoint of improving lateral pressure resistance and wear resistance. parts or less), for example, 0 to 8 parts by mass, preferably 0.1 to 6 parts by mass, more preferably 0.3 to 5 parts by mass, more preferably 0.5 to 4 parts by mass, most preferably is 1 to 3 parts by mass.

(H) inorganic filler (filler)
The rubber composition may further contain an inorganic filler (H). Examples of the inorganic filler (H) include carbonaceous materials (carbon black, graphite, etc.), metal compounds or synthetic ceramics (magnesium oxide, calcium oxide, barium oxide, iron oxide, copper oxide, zinc oxide, titanium oxide, oxide metal oxides such as aluminum; metal silicates such as calcium silicate and aluminum silicate; metal carbides such as silicon carbide and tungsten carbide; metal nitrides such as titanium nitride, aluminum nitride and boron nitride; magnesium carbonate and calcium carbonate Metal carbonates such as; metal sulfates such as calcium sulfate and barium sulfate, etc.), mineral materials (zeolite, diatomaceous earth, calcined diatomaceous earth, activated clay, alumina, silica, talc, mica, kaolin, sericite, bentonite, montmorillonite , smectite, clay, etc.). These inorganic fillers can be used alone or in combination of two or more.

Among these inorganic fillers, carbonaceous materials such as carbon black (first carbon black), metal oxides such as magnesium oxide and zinc oxide (first metal oxide), silica (first silica), etc. is preferable, and it is particularly preferable to contain at least carbon black in terms of improving the hardness, modulus and wear resistance of the cured product of the rubber composition.

Examples of carbon black include SAF, ISAF, HAF, FEF, GPF and HMF. These carbon blacks can be used alone or in combination of two or more. Among these, HAF is preferable because it has a good balance between reinforcing effect and dispersibility and can improve wear resistance.

The average particle size of the carbon black can be selected, for example, from the range of about 5 to 200 nm, for example, about 10 to 150 nm, preferably 15 to 100 nm, more preferably about 20 to 80 nm (especially 30 to 50 nm). If the average particle size of the carbon black is too small, uniform dispersion may become difficult, and if it is too large, the hardness, modulus and abrasion resistance may decrease.

Silica includes dry silica, wet silica, surface-treated silica, and the like. Silica can also be classified into, for example, dry method white carbon, wet method white carbon, colloidal silica, precipitated silica, gel method silica (silica gel), and the like, depending on the production method. These silicas can be used alone or in combination of two or more. Among these, wet process white carbon containing hydrous silicic acid as a main component is preferable because it has many surface silanol groups and strong chemical bonding force with rubber.

The average particle size of silica is, for example, 1 to 1000 nm, preferably 3 to 300 nm, more preferably 5 to 100 nm, more preferably 10 to 50 nm. If the particle size of silica is too large, the mechanical properties of the rubber may deteriorate, and if it is too small, it may be difficult to disperse it uniformly.

Silica may be either non-porous or porous, but has a nitrogen adsorption specific surface area determined by the BET method of, for example, 50 to 400 m ² /g, preferably 70 to 350 m ² /g, more preferably 100 m 2 /g. ~300 m ² /g, more preferably 150-250 m ² /g. If the specific surface area is too large, it may become difficult to disperse uniformly, and if the specific surface area is too small, the mechanical properties of the rubber may deteriorate.

The total proportion of the inorganic filler (H) can be selected from a range of about 10 to 150 parts by weight with respect to 100 parts by weight of the polymer component (A), for example 40 to 100 parts by weight, preferably 50 to 90 parts by weight, More preferably, it is 70 to 80 parts by mass. If the proportion of the inorganic filler (H) is too low, the hardness, modulus and wear resistance of the cured product of the rubber composition may decrease. be.

When the inorganic filler (H) contains carbon black and a metal oxide, the ratio of the metal oxide is, for example, 1 to 100 parts by mass, preferably 3 to 50 parts by mass, with respect to 100 parts by mass of carbon black, and further It is preferably 5 to 30 parts by weight, most preferably 10 to 20 parts by weight.

(I) Other components The rubber composition may further contain other components (I). Other components (I) include conventional additives blended with rubber, such as cross-linking retarders, anti-aging agents (antioxidants, heat anti-aging agents, flex crack inhibitors, anti-ozonants, etc.). , colorants, tackifiers, lubricants, coupling agents (silane coupling agents, etc.), stabilizers (ultraviolet absorbers, heat stabilizers, etc.), flame retardants, antistatic agents, and the like. These additives can be used alone or in combination of two or more. Among these, anti-aging agents (first anti-aging agents) and the like are commonly used.

The total proportion of the other component (I) is, for example, 0.1 to 15 parts by mass, preferably 0.3 to 10 parts by mass, more preferably 0.5 to 100 parts by mass with respect to 100 parts by mass of the polymer component (A). 7 parts by mass. The proportion of the antioxidant is, for example, 0.1 to 5 parts by mass, preferably 0.2 to 3 parts by mass, and more preferably 0.3 to 1 part by mass with respect to 100 parts by mass of the polymer component (A). be.

(J) Properties of Cured Rubber Composition The cured rubber composition has elongation at break necessary for transmission V-belts in spite of its high rubber hardness and modulus. That is, the cured product can achieve both improvement in rubber hardness and modulus, which are in a trade-off relationship, and resistance to bending fatigue. For example, in Patent Document 1, examples with high hardness have low elongation at break, and examples with high elongation at break have low hardness, and these physical properties are not compatible. On the other hand, in the present invention, by satisfying these physical properties, lateral pressure resistance, wear resistance, and bending fatigue resistance can be improved at the same time, and the durability of the transmission V-belt can be improved.

Specifically, the rubber hardness (JIS-A) of the cured product of the rubber composition [rubber hardness containing short fibers in the cured product containing short fibers (C)] is 91 degrees or more, for example 91 to 98 degrees, It is preferably 91.5 to 97 degrees, more preferably 92 to 96 degrees, more preferably 92.5 to 95 degrees, and most preferably 93 to 94 degrees. If the hardness of the short fiber-containing rubber is too low, the lateral pressure resistance and abrasion resistance are lowered.

The cured rubber composition of the rubber composition excluding the short fibers (C) [rubber composition not containing the short fibers (C)] also has a high rubber hardness (matrix rubber hardness). Matrix rubber hardness (JIS-A) may be 83 degrees or more, for example, 83 to 95 degrees, preferably 83.5 to 93 degrees, more preferably 84 to 90 degrees, more preferably 85 to 89 degrees, most preferably 86 to 88 degrees. If the matrix rubber hardness is too low, the lateral pressure resistance and wear resistance may deteriorate.

The difference between the hardness of the rubber containing short fibers and the hardness of the matrix rubber may be 10 degrees or less, preferably 9.5 degrees or less, more preferably 9 degrees or less, more preferably 8 degrees or less, and most preferably 7 degrees. It is below. If the difference is too large, the wear resistance of the belt may deteriorate.

In the present application, the rubber hardness (JIS-A) is measured in accordance with JIS K 6253 (2012) for a cured product press-crosslinked at a temperature of 170° C. and a pressure of 2 MPa for 20 minutes. Measured by the method described in the examples.

The cured product of the rubber composition [cured product containing short fibers (C)] has an elongation at break in the belt longitudinal direction of 100% or more, for example, 100 to 200%, preferably 101 to 180%, more preferably 102 to 102%. 160%, more preferably 103-150%, most preferably 104-130%. If the elongation at break is too small, the bending fatigue resistance is lowered.

In the present application, the elongation at break is measured according to JIS K 6251 (2017), and more specifically, by the method described in Examples below.

The cured product of the rubber composition [cured product containing the short fibers (C)] is also excellent in lateral pressure resistance and has a high 8% bending stress. The 8% bending stress may be 5 MPa or more, for example 5-30 MPa, preferably 5.5-20 MPa, more preferably 6-15 MPa, more preferably 6.5-10 MPa, most preferably 7-9 MPa. be.

In the present application, the 8% bending stress is measured by the method described in Examples below.

[Transmission V-belt]
The transmission V-belt of the present invention may be either a wrapped V-belt or a low-edge type V-belt, but the low-edge type V-belt is preferable because it can improve bending fatigue resistance while ensuring lateral pressure resistance. .

Raw edge type V-belts include raw edge V-belts and raw edge cogged V-belts. Further, the low edge cogged V-belt includes a low edge cogged V belt in which cogs are formed only on the inner peripheral side of the low edge V belt, and a low edge double cog in which cogs are formed on both the inner peripheral side and the outer peripheral side of the low edge V belt. It can be roughly classified into a de V belt. Among these, low edge cogged V-belts and low edge double cogged V-belts are preferred because they are required to have both lateral pressure resistance and bending fatigue resistance at a high level, and are used in more severe situations, A low-edge double cogged V-belt is particularly preferred because it requires a high level of performance. A cogged V-belt is a V-belt in which the side surface of a compression rubber layer is in contact with a pulley, and is particularly preferably a variable speed belt used in a transmission in which the speed change ratio changes steplessly during belt running. It is also preferred that the V-belt is a low edge type V-belt used in a layout including reverse bending.

FIG. 1 is a schematic partial cross-sectional perspective view showing an example of the raw edge cogged V-belt of the present invention, and FIG. 2 is a schematic cross-sectional view of the raw edge cogged V-belt of FIG. 1 cut in the belt longitudinal direction.

In this example, the raw-edge cogged V-belt 1 has cog crests 1a and cog troughs 1b arranged alternately along the longitudinal direction of the belt (direction A in the figure) on the inner peripheral surface of the belt body. The cross-sectional shape of the cog ridge 1a in the longitudinal direction is substantially semicircular (curved or wavy), and the direction perpendicular to the longitudinal direction (the width direction or the B direction in the figure) ) is trapezoidal. That is, each cog ridge 1a protrudes from the cog trough 1b in a substantially semicircular cross section in the A direction in the belt thickness direction. The raw edge cogged V-belt 1 has a laminated structure, and from the outer circumference of the belt to the inner circumference (the side where the cog portion is formed), the first reinforcing cloth 2, the stretch rubber layer 3, the adhesive rubber A layer 4, a compression rubber layer 5 and a second reinforcing fabric 6 are laminated in order. The cross-sectional shape in the belt width direction is a trapezoidal shape in which the belt width decreases from the belt outer circumference side to the belt inner circumference side. Further, a core 4a is embedded in the adhesive rubber layer 4, and the cog portion is formed in the compression rubber layer 5 by a mold with a cog.

The height and pitch of the cogs are similar to those of conventional cogged V-belts. In the compression rubber layer, the height of the cog portion (the height of the cog crest based on the cog valley) is about 50 to 95% (especially 60 to 80%) of the thickness of the entire compression rubber layer. The pitch of the portions (the distance between the central portions of adjacent cog portions) is about 50 to 250% (especially 80 to 200%) of the height of the cog portions. The same is true when forming the cog portion in the stretchable rubber layer.

The overall belt thickness (average thickness) of the raw edge type V-belt of the present invention may be 8 mm or more, for example, 8 to 50 mm, preferably 9 to 45 mm (especially 10 to 40 mm), more preferably 10 to 36 mm ( 11 to 32 mm). These thickness ranges may be selected according to the application, and in low edge type V belts used for motorcycles, snowmobiles, etc., the thickness of the entire belt is, for example, 8 to 18 mm, preferably 10 to 14 mm, more preferably is 11-13 mm. In addition, in low edge type V-belts (especially speed change belts) used in large agricultural machines, the thickness of the entire belt may be 18 mm or more, for example 18 to 40 mm, preferably 19 to 38 mm, more preferably 19 mm. 8 to 36 mm, more preferably 19.8 to 30.5 mm. Since the low edge type V-belt of the present invention can achieve both lateral pressure resistance and bending fatigue resistance, it is particularly suitable for a low edge type V-belt having a large thickness of 18 mm or more. If the thickness is too thin, there is a risk that the lateral pressure resistance will decrease, and if it is too thick, there is a risk that flexibility will decrease, transmission efficiency will decrease, and bending fatigue resistance will decrease.

In the present application, when the compression rubber layer and/or the extension rubber layer has cog portions, the thickness of the entire belt means the thickness at the top of the cog portions (the maximum thickness of the belt).

In the raw edge type V-belt of the present invention, it is preferable that the compression rubber layer and/or the extension rubber layer are formed of the cured rubber composition, and at least the compression rubber layer is formed of the cured rubber composition. More preferably, both the compressed rubber layer and the stretched rubber layer are formed of the cured rubber composition.

(Adhesive rubber layer)
The raw edge type V-belt of the present invention may not include an adhesive rubber layer, but the adhesion between the core and the compression rubber layer, between the core and the extension rubber layer (or the extension rubber layer main body) is increased, and the core is It is preferable to include an adhesive rubber layer from the viewpoint of suppressing separation between the body and the layer. The adhesive rubber layer may be formed of a rubber composition (second rubber composition) containing a polymer component (a) containing an ethylene-α-olefin elastomer and a cross-linking agent (b) containing a sulfur-based cross-linking agent. .

(a) Polymer component The ethylene-α-olefin elastomer (second ethylene-α-olefin elastomer), including preferred aspects (aspects other than diene content), is ethylene exemplified in the section of the polymer component (A). - α-olefin elastomers.

The diene content of the second ethylene-α-olefin elastomer (especially ethylene-α-olefin-diene terpolymer rubber such as EPDM) is 15% by mass or less (for example, 0.5 to 15% by mass). well, preferably 10% by mass or less (eg 1 to 10% by mass), more preferably 8% by mass or less (eg 3 to 8% by mass), more preferably 7% by mass or less (eg 3.5 to 7% by mass) ), most preferably 5% by mass or less (eg, 4 to 5% by mass). If the diene content is too high, there is a risk that high heat resistance cannot be ensured.

Polymer component (a) may also contain other rubber components in addition to the second ethylene-α-olefin elastomer. Other rubber components and their proportions [proportions in the polymer component (B)] can be selected from the other rubber components and their proportions exemplified in the section of the polymer component (A).

(b) Cross-linking agent The sulfur-based cross-linking agent (second sulfur-based cross-linking agent) can be selected from the sulfur-based cross-linking agents exemplified in the above section of cross-linking agent (B), including preferred embodiments.

The ratio of the second sulfur-based cross-linking agent is, for example, 0.1 to 5 parts by mass, preferably 0.3 to 3 parts by mass, more preferably 0.5 to 1 part by mass with respect to 100 parts by mass of the polymer component (a). 0.5 parts by weight, more preferably 0.6 to 1.3 parts by weight, most preferably 0.8 to 1.2 parts by weight. If the proportion of the sulfur-based cross-linking agent is too low, the rubber hardness and lateral pressure resistance may decrease. In addition, there is a possibility that the adhesiveness may be lowered.

The cross-linking agent (b) may also contain an organic peroxide in addition to the second sulfur-based cross-linking agent. The organic peroxide and its proportion can be selected from the organic peroxides and their proportions exemplified in the section of the cross-linking agent (B).

The proportion of the second sulfur-based cross-linking agent in the cross-linking agent (b) may be 50% by mass or more, preferably 70% by mass or more, more preferably 90% by mass or more, and more preferably 100% by mass. .

The ratio of the cross-linking agent (b) is, for example, 0.1 to 5 parts by mass, preferably 0.3 to 3 parts by mass, more preferably 0.5 to 1.5 parts by mass with respect to 100 parts by mass of the polymer component (a). parts by weight, more preferably 0.6 to 1.3 parts by weight, most preferably 0.8 to 1.2 parts by weight.

(c) Short fibers The second rubber composition may further contain short fibers (c). The short fibers (c) can be selected from the short fibers exemplified in the above section of the short fibers (C), including preferred aspects (aspects other than proportions).

The ratio of the short fibers (c) is, for example, 100 parts by mass or less, preferably 50 parts by mass or less, and more preferably 10 parts by mass or less with respect to 100 parts by mass of the polymer component (a). The second rubber composition preferably contains substantially no short fibers (c), more preferably no short fibers (c).

(d) Crosslinking accelerator The second rubber composition may further contain a crosslinking accelerator (d). The cross-linking accelerator (d) can be selected from the cross-linking accelerators exemplified in the above section of the cross-linking accelerator (D), including preferred aspects (aspects other than proportion).

A sulfur-containing cross-linking accelerator (especially a thiomorpholine-based accelerator) in which the cross-linking accelerator (d) has an oxygen- and nitrogen-containing heterocycle, and other sulfur-containing cross-linking accelerators (especially a thiuram-based accelerator and/or sulfen amide accelerator), the mass ratio of the former/latter = 1/99 to 90/10, preferably 5/95 to 70/30, more preferably 10/90 to 50/50 , more preferably 20/80 to 30/70.

The ratio of the sulfur-containing accelerator (second sulfur-containing accelerator) contained in the cross-linking accelerator (d) [the ratio in the cross-linking accelerator (d)] is the same as that of the first sulfur-containing accelerator, including preferred embodiments. You can choose from percentages.

The ratio of the cross-linking accelerator (d) is, for example, 0.1 to 10 parts by mass, preferably 0.3 to 7 parts by mass, more preferably 0.5 to 5 parts by mass with respect to 100 parts by mass of the polymer component (a). parts, more preferably 1 to 3 parts by weight, most preferably 1.5 to 2.5 parts by weight.

(e) Co-crosslinking agent The second rubber composition may further contain a co-crosslinking agent (e). The co-crosslinking agent (e) can be selected from the co-crosslinking agents exemplified in the above section of the co-crosslinking agent (E), including preferred aspects (aspects other than proportions).

The proportion of the co-crosslinking agent (e) is, for example, 100 parts by mass or less, preferably 50 parts by mass or less, and more preferably 10 parts by mass or less with respect to 100 parts by mass of the polymer component (a). The second rubber composition preferably does not substantially contain the co-crosslinking agent (e), and more preferably does not contain the co-crosslinking agent (e).

(f) Adhesion Improver The second rubber composition may further contain an adhesion improver (f). The adhesion improver (f) can be selected from the adhesion improvers exemplified in the section of the adhesion improver (F).

Among the adhesion improvers, the adhesion improver (f) is preferably a resorcinol-formaldehyde resin or a melamine resin, and particularly preferably a combination of a resorcinol-formaldehyde resin and a melamine resin.

When the adhesion improver (f) is a combination of a resorcinol-formaldehyde resin and a melamine resin, the ratio of the resorcinol-formaldehyde resin can be selected from the range of about 10 to 1000 parts by weight with respect to 100 parts by weight of the melamine resin. For example, it is 20 to 300 parts by mass, preferably 30 to 100 parts by mass, more preferably 50 to 80 parts by mass.

The proportion of the adhesion improver (f) can be selected, for example, from a range of about 0.1 to 30 parts by mass, for example, 0.5 to 20 parts by mass, preferably 1 part per 100 parts by mass of the polymer component (a). to 15 parts by mass, more preferably 2 to 10 parts by mass, more preferably 3 to 8 parts by mass.

(g) Softener The second rubber composition may further contain a softener (g). The softener (g) can be selected from the softeners exemplified in the softener (G) section above. Among the above softeners, the softener (g) is preferably a petroleum softener such as paraffin oil.

The ratio of the softening agent (g) may be 1 part by mass or more with respect to 100 parts by mass of the polymer component (a), for example, 1 to 50 parts by mass, preferably 2 to 30 parts by mass, from the viewpoint of improving adhesiveness. parts by mass, more preferably 3 to 20 parts by mass, more preferably 5 to 15 parts by mass, and most preferably 8 to 12 parts by mass.

(h) Inorganic filler The second rubber composition may further contain an inorganic filler (h). The inorganic filler (h) can be selected from the inorganic fillers exemplified in the inorganic filler (H) section.

Among the inorganic fillers, the inorganic filler (h) is preferably a carbonaceous material such as carbon black, a mineral material such as silica, or a metal oxide such as zinc oxide. A combination of carbon black (second carbon black), silica (second silica), and metal oxide (second metal oxide) is particularly preferred because it is possible to achieve both properties and adhesiveness.

The second carbon black can be selected from the first carbon blacks exemplified in the inorganic filler (H) section. Among the carbon blacks, FEF is preferable as the second carbon black from the viewpoint of adhesiveness and the like. The average particle size of the second carbon black can be selected from the average particle size of the first carbon black, including preferred embodiments.

The second silica can be selected from the first silicas exemplified in the inorganic filler (H) section, including preferred embodiments.

The proportion of the second silica is, for example, 5 to 200 parts by weight, preferably 10 to 100 parts by weight, more preferably 30 to 80 parts by weight, more preferably 40 to 60 parts by weight, with respect to 100 parts by weight of the second carbon black. part by mass. If the proportion of silica is too low, the effect of improving adhesion may not be exhibited.

The ratio of the second metal oxide is, for example, 1 to 100 parts by mass, preferably 3 to 50 parts by mass, more preferably 5 to 30 parts by mass, most preferably 10 parts by mass, with respect to 100 parts by mass of the second carbon black. ~20 parts by mass.

The total proportion of the inorganic filler (h) can be selected from a range of about 10 to 100 parts by weight with respect to 100 parts by weight of the polymer component (a), for example 20 to 80 parts by weight, preferably 30 to 70 parts by weight, More preferably 40 to 60 parts by mass. If the proportion of the inorganic filler is too small, the elastic modulus may be insufficient and the lateral pressure resistance may be lowered.

(i) Other components The second rubber composition may further contain other components (i). The other component (i) can be selected from the other components exemplified in the section of the other component (I) above.

The total proportion of the other component (i) is, for example, 0.1 to 15 parts by mass, preferably 0.3 to 10 parts by mass, more preferably 0.5 to 100 parts by mass, relative to 100 parts by mass of the polymer component (a). 7 parts by mass. The ratio of the antioxidant (second antioxidant) is, for example, 0.1 to 10 parts by mass, preferably 0.5 to 5 parts by mass, more preferably 0.5 to 5 parts by mass, with respect to 100 parts by mass of the polymer component (a). 1 to 3 parts by mass.

[Core body]
The core body is not particularly limited, but usually core wires (twisted cords) arranged at predetermined intervals in the belt width direction can be used. The cords are arranged to extend in the longitudinal direction of the belt, and are generally arranged in parallel with the longitudinal direction of the belt at a predetermined pitch. At least a part of the cord may be in contact with the adhesive rubber layer. It may be of any form in which the cord is embedded between the layer and the compression rubber layer. Among these, the configuration in which the core wire is embedded in the adhesive rubber layer is preferable from the viewpoint of improving the durability. In the case of a V-belt having no adhesive rubber layer, the cord may be embedded between the tension rubber layer and the compression rubber layer.

As the material of the fiber constituting the core wire, the material of the short fibers exemplified in the section of the short fiber (C) can be used. Among the fibers having the above materials, from the viewpoint of high modulus, polyester fibers (polyalkylene arylate fibers) having C _2-4 alkylene-arylates such as ethylene terephthalate and ethylene-2,6-naphthalate as main structural units (polyalkylene arylate fibers), aramid Synthetic fibers such as fibers and inorganic fibers such as carbon fibers are widely used, and polyester fibers (polyethylene terephthalate-based fibers, polyethylene naphthalate-based fibers, etc.) and polyamide fibers are preferred.

Twisted cords using multifilament yarns (for example, plied, single-twisted, Lang-twisted, etc.) can be used as the cord. The total fineness of the twisted cord may be, for example, 2200-13500 dtex (especially 6600-11000 dtex). The twisted cord may contain, for example, 1000-10000 monofilaments, preferably 2000-8000, more preferably 4000-6000 monofilaments. The average wire diameter of the cord (diameter of the twisted cord) may be, for example, 0.5 to 3 mm, preferably 0.6 to 2 mm, and more preferably about 0.7 to 1.5 mm. .

The core wire may be subjected to adhesion treatment (or surface treatment) in the same manner as the short fibers in order to improve adhesion with the rubber component. It is preferred that the cords be treated with at least RFL liquid.

[Reinforcing cloth]
When the raw edge type V-belt of the present invention includes a reinforcing fabric, for example, both the compression rubber layer and the extension rubber layer (the cog when the cog is formed integrally with the compression rubber layer) (the inner circumference of the compression rubber layer surface and the outer peripheral surface of the stretched rubber layer); Examples include a form in which a reinforcing layer is embedded in a rubber layer (for example, a form described in JP-A-2010-230146). A form in which the reinforcing cloth is laminated on the surface of at least one of the compressed rubber layer and the stretched rubber layer (the inner peripheral surface of the compressed rubber layer and the outer peripheral surface of the stretched rubber layer), for example, the inner peripheral surface of the compressed rubber layer. In many cases, it is laminated on both the (lower surface) and the outer peripheral surface (upper surface) of the stretched rubber layer.

The reinforcing fabric can be formed of, for example, a fabric material (especially a woven fabric) such as a woven fabric, a wide-angle canvas, a knitted fabric, and a nonwoven fabric, and if necessary, is subjected to adhesion treatment, for example, treatment with an RFL liquid (immersion treatment, etc. ), the friction treatment of rubbing the adhesive rubber into the cloth material, or the adhesive rubber and the cloth material are laminated (coated) and then laminated or embedded in the compression rubber layer and/or the extension rubber layer in the above-described form. may

[Manufacturing method of transmission V-belt]
The method of manufacturing the power transmission V-belt of the present invention is not particularly limited, and conventional methods can be used. In the case of a raw-edge cogged V-belt, for example, a laminate consisting of a reinforcing cloth (lower cloth) and a compressed rubber layer sheet (uncrosslinked rubber sheet) is arranged alternately in teeth and grooves with the reinforcing cloth facing downward. The cog pad is placed in a flat mold with cogs and pressed at a temperature of about 60 to 100°C (especially 70 to 80°C) to mold the cog part (not completely crosslinked, semi-crosslinked). After making the cog pad, the ends of the cog pad may be cut vertically from the top of the cog peaks. Furthermore, the cylindrical mold is covered with an inner matrix (a mold made of cross-linked rubber) in which teeth and grooves are alternately arranged. After laminating the first adhesive rubber layer sheet (lower adhesive rubber: uncrosslinked rubber sheet) on the wound cog pad, the core wire (twisted cord) forming the core is spirally Then, a second adhesive rubber layer sheet (upper adhesive rubber: the same as the adhesive rubber layer sheet), a stretched rubber layer sheet (uncrosslinked rubber sheet), and a reinforcing cloth (upper cloth) are sequentially laid thereon. A compact may be produced by winding. After that, a jacket (jacket made of crosslinked rubber) was placed on the mold, and the mold was placed in a vulcanization can, and crosslinked at a temperature of 120 to 200°C (especially 150 to 180°C) to prepare a belt sleeve. After that, a cutting step may be performed in which a compressed rubber layer is formed by cutting with a cutter or the like so as to have a V-shaped cross section.

For raw-edge cogged V-belts that do not contain reinforcing fabrics, a laminate may be prepared by pre-pressing a sheet for the compression rubber layer and a sheet for the first adhesive rubber layer.

In the stretched rubber layer sheet and the compressed rubber layer sheet, as a method for orienting the orientation direction of the short fibers in the belt width direction, a conventional method, for example, a rubber roll between a pair of calender rolls provided with a predetermined gap, is used. Both sides of the rolled sheet with short fibers oriented in the rolling direction are cut parallel to the rolling direction, and the rolled sheet is rolled so as to have a belt forming width (length in the belt width direction). A method of cutting in a direction perpendicular to the direction and jointing the side surfaces cut in a direction parallel to the rolling direction can be used. For example, the method described in JP-A-2003-14054 can be used. The uncrosslinked sheet in which the short fibers are oriented by such a method is arranged and crosslinked in the above-described method so that the orientation direction of the short fibers is the width direction of the belt.

EXAMPLES The present invention will be described in more detail below based on examples, but the present invention is not limited by these examples. Details of raw materials used in the examples are shown below.

[material]
(polymer component)
EPDM1: "EP93" manufactured by JSR Corporation, ethylene content 55% by mass, diene content 2.7% by mass
EPDM2: "EP24" manufactured by JSR Corporation, ethylene content 54% by mass, diene content 4.5% by mass.

(Cross-linking agent, cross-linking accelerator and cross-linking aid)
Sulfur: "Powder Sulfur" manufactured by Bigen Chemical Co., Ltd.
Organic peroxide: "P-40MB (K)" manufactured by NOF Corporation
Crosslinking accelerator A: Ouchi Shinko Kagaku Kogyo Co., Ltd. "Noccellar TT"
Crosslinking accelerator B: "Noccellar CZ" manufactured by Ouchi Shinko Kagaku Kogyo Co., Ltd.
Crosslinking accelerator C: Ouchi Shinko Kagaku Kogyo Co., Ltd. "Balnok R"
Co-crosslinking agent A (bismaleimide): "Balnok PM" manufactured by Ouchi Shinko Kagaku Kogyo Co., Ltd.
Co-crosslinking agent B (zinc methacrylate): "Sunester SK-30" manufactured by Sanshin Chemical Industry Co., Ltd.

(fiber member)
Para-aramid staple fiber: manufactured by Teijin Limited, Twaron cut yarn, average fiber length 3 mm
Nylon staple fiber: Asahi Kasei Corp., Leona cut yarn, average fiber length 3 mm
Core wire: Two multifilament bundles of aramid fibers with a fineness of 1,680 dtex were aligned and under-twisted to prepare a first-twisted yarn, and the three prepared first-twisted yarns were combined and p-twisted in the opposite direction to the first twist. Ply-twisted cord with a total fineness of 10,080 dtex Reinforcing cloth: Nylon canvas of composition 2/2 twill weave (thickness 0.50 mm).

(other ingredients)
Carbon black A (HAF): "N330" manufactured by Cabot Japan Co., Ltd.
Carbon black B (FEF): "N550" manufactured by Cabot Japan Co., Ltd.
Silica: "Ultrasil VN3" manufactured by Evonik Degussa Japan Co., Ltd., BET specific surface area 175 m ² /g
Paraffin oil: "Diana Process Oil PW90" manufactured by Idemitsu Kosan Co., Ltd.
Antiaging agent A: "Nocrac CD" manufactured by Ouchi Shinko Kagaku Kogyo Co., Ltd.
Antiaging agent B: "Nonflex OD3" manufactured by Seiko Chemical Co., Ltd.
Zinc oxide: "Type 2 zinc oxide" manufactured by Sakai Chemical Industry Co., Ltd.
Stearic acid: "Tsubaki Stearate" manufactured by NOF Corporation
Magnesium oxide: "Kyowamag 150" manufactured by Kyowa Chemical Industry Co., Ltd.
Adhesion improver A (resorcinol-formaldehyde resin): Singh Plasticisers & Resins Pvt. Ltd. "POWERPLAST PP-1860" manufactured by
Adhesion improver B (hexamethoxymethylmelamine): Singh Plasticisers & Resins Pvt. Ltd. "POWERPLAST PP-1890S" manufactured by the company.

Examples 1-9 and Comparative Examples 1-4
[Rubber hardness]
An uncrosslinked rubber sheet having the composition shown in Table 1 was press-crosslinked at a temperature of 170° C., a pressure of 2 MPa, and a time of 20 minutes to prepare a crosslinked rubber sheet (100 mm×100 mm×2 mm thickness). The rubber hardness was measured according to JIS K 6253 (2012) using a durometer type A hardness tester using a laminate obtained by stacking three crosslinked rubber sheets as a sample. The matrix rubber hardness was measured in the same manner, except that a crosslinked rubber sheet containing no short fibers was produced by excluding short fibers from the above formulation. Table 3 shows the results.

[Breaking elongation]
An uncrosslinked rubber sheet having the composition shown in Table 1 was press-crosslinked at a temperature of 170° C., a pressure of 2 MPa, and a time of 20 minutes to prepare a crosslinked rubber sheet (100 mm×100 mm×2 mm thickness). This crosslinked rubber sheet was punched out with a super dumbbell cutter manufactured by Dumbbell Co., Ltd. to prepare a dumbbell-shaped No. 3 test piece. Using the prepared test piece, the elongation at break was measured according to JIS K 6251 (2017). The tensile speed was 500 mm/min, and the test temperature was 23°C. The measurement was carried out in a direction (perpendicular to the grain) in which the longitudinal direction of the test piece and the grain (longitudinal direction of the short fibers) were perpendicular to each other. Table 3 shows the results.

[8% bending stress]
An uncrosslinked rubber composition having the composition shown in Table 1 was press-crosslinked at a temperature of 170° C., a pressure of 2 MPa, and a time of 20 minutes to prepare a crosslinked rubber molding (60 mm×25 mm×6.5 mm thick). The short fibers were oriented parallel to the longitudinal direction of the crosslinked rubber molding. As shown in FIG. 3, this crosslinked rubber molded body 21 is placed on and supported by a pair of rotatable rolls (6 mm in diameter) 22a and 22b with an interval of 20 mm. , a metal pressing member 23 was placed in the width direction (direction perpendicular to the orientation direction of the short fibers). The tip of the pressing member 23 has a semicircular shape with a diameter of 10 mm, and the tip can press the crosslinked rubber molding 21 smoothly. When pressed, frictional force acts between the lower surface of the crosslinked rubber molded body 21 and the rolls 22a and 22b as the crosslinked rubber molded body 21 is compressed and deformed. , which reduces the effect of friction. A state in which the tip of the pressing member 23 is in contact with the upper surface of the crosslinked rubber molded body 21 and is not pressed is the initial position, and from this state, the pressing member 23 is moved downward at a rate of 100 mm/min to remove the crosslinked rubber molded body 21. The stress when the upper surface was pressed and the bending strain reached 8% was measured as the bending stress. By measuring the bending stress in the direction perpendicular to the orientation direction of the short fibers, it can be judged that the resistance to buckling deformation called dishing during belt running is high when the bending stress is high, and high load transmission and high durability It can be used as an indicator of gender. The measured temperature was 120° C. assuming the temperature of the belt during running.

[Presence or absence of sheet bloom]
An uncrosslinked rubber composition rolled into a sheet having a thickness of 2 mm was allowed to stand at 25° C. for 14 days, and the rubber surface was visually observed to confirm the presence or absence of bloom (precipitation of additives such as a cross-linking agent on the sheet surface). . In general, even if blooming occurs, the physical properties of the rubber do not change significantly.

[Belt production]
On the surface of the inner matrix made of crosslinked rubber with a cog shape attached to the mold, the cog part is formed by molding the laminate obtained by laminating the sheet for the compressed rubber layer having the composition shown in Table 1 and having a predetermined thickness and the reinforcing cloth in advance. After winding and jointing the sheet-shaped cog pads, the lower adhesive rubber sheet having the composition shown in Table 2, the cord, the upper adhesive rubber sheet having the composition shown in Table 2, and the flat sheet having the composition shown in Table 1 A molded product was produced by sequentially winding the stretchable rubber layer sheet. Subsequently, the surface of the molded product was covered with an outer mold made of crosslinked rubber with a cog shape and a jacket, the mold was placed in a vulcanizing can, and crosslinked at a temperature of 170° C. for 40 minutes at 0.9 MPa. Got a belt sleeve. As the crosslinking conditions, conditions similar to the crosslinking of the uncrosslinked sheet for the adhesive rubber layer, the sheet for the compressed rubber layer and the sheet for the stretched rubber layer were selected. This sleeve was cut into a V-shape by a cutter to finish a transmission belt. That is, a low-edge double-cogged V-belt having the structure shown in FIG. 4 was produced (reinforcing fabric not shown). Specifically, in a low edge double cogged V-belt in which a compression rubber layer 13 and a tension rubber layer 14 are formed on both sides of an adhesive rubber layer 11 in which a core wire 12 is embedded, either the compression rubber layer 13 or the tension rubber layer 14 Also, a belt (size: upper width 20 mm, thickness 10 mm, outer circumference length 817 mm) on which cog portions 16 and 17 are respectively formed was produced. Table 3 shows the results of the following evaluation tests performed on the obtained low edge double cogged V-belt.

[Two-axis endurance running test]
The biaxial durability running test was conducted using a biaxial running test machine including a drive (Dr.) pulley with a diameter of 50 mm and a driven (Dn.) pulley with a diameter of 125 mm, as shown in FIG. A low-edge cogged V-belt was stretched over each pulley, the rotation speed of the driving pulley was 5,600 rpm, the load of the driven pulley was 22.8 N·m, and the belt was run at an ambient temperature of 80° C. for 72 hours. After running, the side surface of the low-edge double cogged V-belt (the surface in contact with the pulley) was visually observed to check for peeling between the cord and the adhesive rubber layer. Also, the amount of change in the upper width of the low edge double cogged V-belt before and after the running test (upper width before running test - upper width after running test) was determined. It can be judged that the smaller the amount of change in the upper width, the better the wear resistance.

[Reverse bending endurance running test (dynamic reverse bending test)]
As shown in FIG. 6, the reverse bending endurance running test was conducted using a driving (Dr.) pulley with a diameter of 97.6 mm, a driven (Dn.) pulley with a diameter of 77.9 mm, and a rear idler (Id.) with a diameter of 79.4 mm. ) was performed using a triaxial running tester including pulleys. A low-edge double-cogged V-belt is hung on each pulley, and tension is applied to the belt by suspending a weight of 40 kgf on the drive pulley. The central angle) was adjusted to 15°. The rotation speed of the drive pulley was 3,600 rpm, the driven pulley and the rear idler pulley were unloaded, and the ambient temperature was 120° C., and the belt was run until the end of its life. In addition, when the crack depth (the length in the thickness direction of the belt) of the cog valley of the low edge double cogged V-belt became 2 mm or more, the life was judged to have expired. It can be judged that the longer the running time until reaching the end of the service life, the better the bending fatigue resistance.

[Reverse bending crack test (static reverse bending test)]
In the reverse bending crack test, as shown in FIG. 7, the raw edge cogged V belt 30 with the inner and outer peripheral surfaces of the belt reversed is sandwiched between two parallel flat plates, and the two flat plates are separated. The distance between the belts was gradually narrowed at a speed of 50 mm/min, and the distance between the plates was measured when a crack occurred in the cog valley of the low-edge double cogged V-belt. It can be judged that the shorter the plate-to-plate distance when a crack occurs, the better the bending fatigue resistance (crack resistance).

As is clear from the results in Table 3, Comparative Examples 1 and 2 crosslinked with an organic peroxide had a high rubber hardness but a small elongation at break, and were particularly inferior in terms of resistance to bending fatigue. Comparative Example 3 is an example in which the amount of sulfur compounded was reduced, but the rubber hardness was not sufficiently improved, the lateral pressure resistance was lowered, peeling occurred, and the wear resistance was also low. Comparative Example 4 is an example in which the compounding amount of bismaleimide was increased, but the elongation at break and bending fatigue resistance were low.

Examples 1 to 9 had high rubber hardness, high elongation at break, and were able to achieve both wear resistance and bending fatigue resistance, and were excellent in durability. In Example 1, which contained a large amount of paraffinic oil, the wear resistance was slightly lowered. Examples 4 to 9 containing bismaleimide as a co-crosslinking agent had particularly high rubber hardness and excellent abrasion resistance.

From the comparison of Examples 5 to 7, when the sulfur content was low, the wear resistance tended to decrease, and when the sulfur content was high, the bending fatigue resistance tended to decrease. In addition, in Example 7, in which the amount of sulfur compounded was large, bloom occurred in the uncrosslinked rubber sheet. From the comparison of Examples 5, 8, and 9, when the amount of bismaleimide as a co-crosslinking agent is small, the bending stress and abrasion resistance are reduced by 8%, and when the amount of bismaleimide is large, elongation at break and bending resistance are reduced. Fatigue tended to decrease. In Comparative Example 4, in which the amount of bismaleimide compounded was further increased, the elongation at break and bending fatigue resistance decreased to an unacceptable level.

The transmission V-belt of the present invention can be applied to transmission V-belts used in various fields of automobiles and industrial machinery, such as wrapped V-belts and raw edge type V-belts, while ensuring lateral pressure resistance. , it is preferably applied to a low-edge type V-belt because it can improve bending fatigue resistance. As the raw edge type V-belt, a raw edge V-belt, a low edge cogged V-belt having a cog portion (low edge cogged V-belt, low edge double cogged V-belt, etc.) can be applied.

Furthermore, since the power transmission V-belt of the present invention can achieve both lateral pressure resistance and bending fatigue resistance, it can be used in motorcycles, ATVs (four-wheeled buggies), snowmobiles, large agricultural machines, etc. while the belt is running. Suitable for V-belts (transmission belts) used in transmissions (belt-type continuously variable transmissions) where the ratio changes steplessly, and low-edge V-belts used in layouts that include reverse bending. , Abrasion resistance and bending fatigue resistance can be achieved at a high level, so variable speed belts used in large agricultural machines (combines, mowers, etc.) that require high horsepower of 75 kW / or more (for example, in the ASABE standard, It is particularly preferable to apply it to large belts corresponding to HL to HQ).

DESCRIPTION OF SYMBOLS 1... V-belt for power transmission 2, 6... Reinforcement cloth 3... Extension rubber layer 4... Adhesion rubber layer 4a... Core body 5... Compression rubber layer

Claims (12)

A low-edge cogged V-belt containing a cured product of a first rubber composition and having cogs on at least the inner peripheral surface side,
The first rubber composition comprises a polymer component (A) containing an ethylene-α-olefin elastomer, a cross-linking agent (B) containing a sulfur-based cross-linking agent, and short fibers (C),
The ratio of the sulfur-based cross-linking agent is 1.2 parts by mass or more with respect to 100 parts by mass of the polymer component (A),
The short fibers (C) are oriented in the belt width direction,
A raw-edge cogged V-belt, wherein the cured product has a rubber hardness (JIS-A) of 91 degrees or more and a breaking elongation in the longitudinal direction of the belt of 101 to 180% . 2. The raw-edge cogged V-belt according to claim 1, wherein a hardened rubber composition obtained by removing said short fibers (C) from said first rubber composition has a matrix rubber hardness (JIS-A) of 83 degrees or more. 3. The raw edge cogged V-belt according to claim 1 or 2, wherein said first rubber composition further comprises a cross-linking accelerator (D), and said cross-linking accelerator (D) comprises a sulfur-containing cross-linking accelerator. 4. The raw edge cogged V-belt of claim 3, wherein the sulfur-containing accelerator comprises a sulfur-containing accelerator having an oxygen- and nitrogen-containing heterocycle. The raw edge cogged V according to any one of claims 1 to 4, wherein the first rubber composition further comprises a co-crosslinking agent (E), and the co-crosslinking agent (E) comprises a bismaleimide compound. belt. The raw edge cogged V-belt according to any one of claims 1 to 5, wherein said first rubber composition further comprises an adhesion improver (F). The first rubber composition further contains a softening agent (G), and the ratio of the softening agent (G) is 0.1 to 10 parts by mass with respect to 100 parts by mass of the polymer component (A). A raw-edge cogged V-belt according to any one of claims 1-6. The low-edge cogged V-belt according to any one of claims 1 to 7, comprising a compression rubber layer and/or a stretch rubber layer formed of a cured product of said first rubber composition. Further comprising an adhesive rubber layer formed of a cured product of the second rubber composition,
The second rubber composition according to any one of claims 1 to 8, wherein the second rubber composition comprises a polymer component (a) containing an ethylene-α-olefin elastomer and a cross-linking agent (b) containing a sulfur-based cross-linking agent. Raw edge cogged V-belt. A raw edge cogged V-belt according to any one of claims 1 to 9, which is a speed change belt. The raw edge cogged V-belt according to any one of claims 1 to 10, wherein the average thickness of the entire belt is 19.8 to 36 mm. The raw edge cogged V-belt according to any one of claims 1 to 9, which is a raw edge cogged V-belt for use in layouts involving reverse bending.

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