JP2015218248A - Rubber composition, rubber composition metal laminate, and vulcanized rubber product - Google Patents

Abstract

PROBLEM TO BE SOLVED: To provide: a rubber composition with which a rubber layer with excellent adhesiveness to a metal surface can be obtained; a rubber composition metal laminate; and a vulcanized rubber product.SOLUTION: This rubber composition is characterized in comprising, with respect to 100 parts by mass of a diene polymer that is capable of being vulcanized by sulfur, 0.5 parts by mass or more to 5 parts by mass or less of sulfur, and 0.8 parts by mass or more to 17 parts by mass or less of a hydroxy group-containing compound with a molecular weight of 200 or less.

Description

  The present invention relates to a rubber composition, a rubber composition metal laminate, and a vulcanized rubber product, and more particularly to a rubber composition containing a vulcanizing agent, a rubber composition metal laminate, and a vulcanized rubber product.

  Conventionally, a chloroprene-based rubber composition for producing a hydraulic hose and a high-pressure hose in which a reinforcing layer plated with a metal such as brass (brass) is sandwiched between a pair of rubber layers has been proposed (for example, Patent Documents). 1). Since this rubber composition contains a vulcanization accelerator such as sulfur and guanidine, the cross-linking property of the rubber layer made of the rubber composition is improved, and the adhesion between the metal surface of the reinforcing layer and the rubber layer is improved. It becomes good.

JP 2001-279022 A

  By the way, as a manufacturing method of the above-mentioned hose, the rubber composition is vulcanized by heating the rubber composition with steam to vulcanize the rubber composition, and the rubber composition is vulcanized with an oven. There is an oven vulcanization method. The oven vulcanization method can continuously vulcanize, so that the hose productivity can be improved.

  However, when the rubber composition is vulcanized by the oven vulcanization method, moisture is remarkably evaporated during vulcanization, and sufficient adhesion between the rubber layer and the reinforcing layer may not always be obtained. Therefore, a rubber composition that provides a rubber layer having excellent adhesion to the metal surface of the reinforcing layer even when vulcanized not only by a steam vulcanization method but also by a hot air vulcanization method such as an oven vulcanization method. Is desired.

  The present invention has been made in view of such circumstances, and provides a rubber composition, a rubber composition metal laminate, and a vulcanized rubber product from which a rubber layer having excellent adhesion to a metal surface can be obtained. With the goal.

  The rubber composition of the present invention comprises 100 parts by mass of a diene polymer that can be vulcanized with sulfur, 0.5 parts by mass or more and 5 parts by mass or less of sulfur, and 0.8 to 17 parts by mass of a molecular weight. Containing 200 or less hydroxyl-containing compounds.

  According to this rubber composition, since the sulfur content in the rubber composition and the hydroxyl group equivalent derived from the hydroxyl group-containing compound are in an appropriate range, the catalytic function of the bond formation reaction between the sulfur and the metal surface by the hydroxyl group-containing compound. Is efficiently expressed. As a result, this rubber composition can be used with a metal surface such as a reinforcing layer, even when vulcanized using either a hot-air vulcanization method or a steam vulcanization method that makes the composition easy to dry. A rubber layer having excellent adhesiveness can be obtained.

In the rubber composition of the present invention, the hydroxyl group-containing compound is preferably represented by the following general formula (1).
ROH (1)
(In the formula (1), R represents a hydrogen atom, an ether bond, and an alkyl group having 1 to 5 carbon atoms which may contain a branch or an ether bond and a branch having 1 to 10 carbon atoms which may contain an branch. Hereinafter, it represents a hydroxyalkyl group having a hydroxyl group of 5 or less.)

  The rubber composition metal laminate of the present invention comprises a reinforcing layer having a metal surface and a rubber layer containing the rubber composition provided on the metal surface.

  According to this rubber composition metal laminate, since the sulfur content in the rubber composition and the hydroxyl group equivalent derived from the hydroxyl group-containing compound are in an appropriate range, a bond formation reaction between sulfur and the metal surface by the hydroxyl group-containing compound is achieved. The catalytic function is efficiently expressed. As a result, the rubber composition metal laminate can be applied to the metal surface of the reinforcing layer regardless of whether the composition is vulcanized using a hot-air vulcanization method or a steam vulcanization method that allows the composition to dry easily. It is possible to obtain a rubber composition metal laminate having excellent adhesion between the rubber layer and the rubber layer.

  In the rubber composition metal laminate according to the present invention, the metal surface is preferably subjected to brass plating.

  In the rubber composition metal laminate of the present invention, it is preferable that the reinforcing layer has a braided structure in which wires are knitted or a spiral structure.

  The vulcanized rubber product of the present invention is obtained by using the above rubber composition.

  In the vulcanized rubber product of the present invention, it is preferable that the rubber layer of the rubber composition metal laminate is vulcanized in the presence of sulfur and bonded to the reinforcing layer.

  In the vulcanized rubber product of the present invention, a hose is preferable.

  ADVANTAGE OF THE INVENTION According to this invention, the rubber composition from which the rubber layer excellent in adhesiveness with a metal surface is obtained, a rubber composition metal laminated body, and a vulcanized rubber product are realizable.

FIG. 1 is a schematic partially broken perspective view showing an example of a hydraulic hose according to an embodiment of the present invention. Drawing 2 is an explanatory view of the manufacturing process of the hydraulic hose using the rubber composition concerning an embodiment of the invention. FIG. 3 is an explanatory diagram of a vulcanization process of a hydraulic hose using the rubber composition according to the embodiment of the present invention. FIG. 4 is a partial cross-sectional view showing an example of a layer structure around a mandrel that is put into a vulcanizing apparatus in a manufacturing process of a hydraulic hose using the rubber composition according to the embodiment of the present invention.

  Hereinafter, an embodiment of the present invention will be described in detail with reference to the accompanying drawings. In addition, this invention is not limited to the following embodiment, It can implement by changing suitably.

  The rubber composition according to the present embodiment includes 100 parts by mass of a diene polymer that can be vulcanized with sulfur, 0.5 parts by mass to 5 parts by mass of sulfur, and 0.8 parts by mass to 17 parts by mass. And a hydroxyl group-containing compound having a molecular weight of 200 or less.

  According to this rubber composition, since the diene rubber polymer contains a predetermined amount of sulfur and a predetermined amount of a hydroxyl group-containing compound, the sulfur content and the hydroxyl group equivalent in the rubber composition are in an appropriate range, The catalytic function of the bond formation reaction between sulfur and the metal surface by the hydroxyl group-containing compound is efficiently expressed. As a result, this rubber composition has a vulcanization method of either a hot air vulcanization method or a steam vulcanization method in which the composition is easy to dry and water having a catalytic function of a bond formation reaction between sulfur and a metal surface is reduced. Even when vulcanization is performed, it is possible to obtain a rubber layer having excellent adhesion between the metal surface and the rubber layer. Hereinafter, various components of the rubber composition according to the present embodiment will be described in detail.

<Diene polymer>
As the diene polymer, one that can be vulcanized with sulfur is used. Here, sulfur vulcanizable means the property that a crosslinked structure is formed through sulfur. Examples of other diene polymers include natural rubber (NR), chloroprene rubber (CR), isoprene rubber (IR), styrene butadiene rubber (SBR), acrylonitrile-butadiene rubber (NBR), ethylene-propylene-diene rubber ( EPDM), chlorinated polyethylene rubber (CM), and chlorosulfonated polyethylene rubber (CSM). By using these, various physical properties for hoses required for the rubber composition can be exhibited at a high level. Among these, chloroprene rubber (CR), styrene butadiene rubber (SBR), acrylonitrile-butadiene rubber (NBR), ethylene-propylene-diene rubber from the viewpoint of obtaining high adhesion between the metal surface of the reinforcing layer and the rubber layer. (EPDM) is preferred. These diene polymers may be used alone or in combination of two or more.

  The blending amount of the diene polymer is preferably 20% by mass or more and 70% by mass or less with respect to the entire rubber composition from the viewpoint of good rubber mixing processability and good rubber appearance.

<Vulcanizing agent>
The rubber composition according to the present embodiment contains sulfur as a vulcanizing agent. Sulfur includes powdered sulfur, precipitated sulfur, highly dispersible sulfur, surface treated sulfur, and insoluble sulfur.

  The sulfur content is 0.5 parts by mass or more and 5.0 parts by mass or less with respect to 100 parts by mass of the diene polymer. If the sulfur content is 0.5 parts by mass or more and 5.0 parts by mass or less, a bond between sulfur and the metal surface is sufficiently formed at the time of vulcanization of the rubber composition, and the rubber layer and the metal surface are sufficiently bonded. Adhesiveness is obtained. From the viewpoint of adhesion between the rubber layer and the metal surface, the sulfur content is preferably 0.55 parts by mass or more, more preferably 0.6 parts by mass or more, based on 100 parts by mass of the diene polymer. .65 parts by mass or more is more preferable, 0.7 parts by mass or more is more preferable, 3.75 parts by mass or less is preferable, 3.5 parts by mass or less is more preferable, and 3.25 parts by mass or less is more preferable. 3.0 mass parts or less are still more preferable. Considering the above, the content of sulfur is preferably 0.55 parts by mass or more and 3.75 parts by mass or less, and 0.6 parts by mass or more and 3.5 parts by mass or less with respect to 100 parts by mass of the diene polymer. More preferably, it is 0.65 parts by mass or more and 3.25 parts by mass or less, and more preferably 0.7 parts by mass or more and 3.0 parts by mass or less.

  The rubber composition according to the present embodiment may contain a vulcanizing agent other than sulfur as long as the effects of the present invention are achieved. Examples of vulcanizing agents other than sulfur include vulcanizing agents such as sulfur-based, organic peroxide-based, metal oxide-based, phenolic resin, and quinone dioxime. These may be used alone or in combination of two or more. Examples of the sulfur-based vulcanizing agent include tetramethyl thiuram disulfide (TMTD), tetraethyl thiuram disulfide (TETD), tetrabutyl thiuram disulfide (TBTD), dipentamethylene thiuram tetrasulfide (DPTT), tetrabenzyl thiuram disulfide, and Examples thereof include organic sulfur-containing compounds such as dimorpholine disulfide and alkylphenol disulfide.

  Examples of the organic peroxide vulcanizing agent include dicumyl peroxide, benzoyl peroxide, t-butyl hydroperoxide, 2,4-dichlorobenzoyl peroxide, 2,5-dimethyl-2,5-di ( t-butylperoxy) hexane, 2,5-dimethylhexane-2,5-di (peroxylbenzoate).

  Examples of other vulcanizing agents include resins such as zinc white, magnesium oxide, phenol resin, p-quinone dioxime, p-dibenzoylquinone dioxime, poly-p-dinitrosobenzene, and methylene dianiline. Can be mentioned.

<Vulcanization accelerator>
The rubber composition according to the present embodiment preferably further contains a vulcanization accelerator. Examples of the vulcanization accelerator include an aldehyde-ammonia vulcanization accelerator, an aldehyde-amine vulcanization accelerator, a thiourea vulcanization accelerator, a guanidine vulcanization accelerator, a thiazole vulcanization accelerator, and sulfene. Examples include amide vulcanization accelerators, thiuram vulcanization accelerators, dithiocarbamate vulcanization accelerators, and xanthate vulcanization accelerators. These may be used alone or in combination of two or more.

  Examples of the thiuram vulcanization accelerator include tetramethylthiuram monosulfide (TS) and tetramethylthiuram disulfide (TT). Examples of the guanidine vulcanization accelerator include diphenyl guanidine. Examples of the sulfenamide vulcanization accelerator include Nt-butylbenzothiazole-2-sulfenamide. Examples of the thiourea vulcanization accelerator include ethylene thiourea.

  The content of the vulcanization accelerator is 0. From the viewpoint of improving the vulcanization characteristics and improving the adhesion between the rubber layer using the rubber composition and the metal surface with respect to 100 parts by mass of the diene polymer. 5 parts by mass or more is preferable, 0.75 parts by mass or more is more preferable, 1.0 part by mass or more is more preferable, 3.5 parts by mass or less is preferable, 3.0 parts by mass or less is more preferable, and 2.5 More preferred is less than or equal to parts by weight.

<Hydroxyl-containing compound>
As the hydroxyl group-containing compound, various compounds can be used as long as they have a hydroxyl group as long as the effects of the present invention are achieved. Since this hydroxyl group-containing compound has a function of catalyzing a bond formation reaction between sulfur as a vulcanizing agent and metal atoms on the metal surface during vulcanization of the rubber composition, the rubber layer containing the rubber composition and the metal surface Adhesion is improved.

In the rubber composition according to the present embodiment, the hydroxyl group-containing compound is preferably represented by the following general formula (1).
ROH (1)
(In the formula (1), R represents a hydrogen atom, an ether bond and a branched alkyl group having 1 to 5 carbon atoms or a hydroxyalkyl group having 1 to 10 carbon atoms and a hydroxyl group of 5 or less. Represents.)

  In the general formula (1), examples of the alkyl group for R include a methyl group, an ethyl group, an n-propyl group, an i-propyl group, an n-cybutyl group, an s-butyl group, a t-butyl group, and a pentyl group. Hexyl group, heptyl group, octyl group, nonyl group, decyl group and the like. Among these, as the alkyl group of R, from the viewpoint of adhesion between the rubber layer using the rubber composition and the metal surface, a methyl group, an ethyl group, an n-propyl group, an i-propyl group, an n-cybutyl group , S-butyl group, t-butyl group and pentyl group are preferable, and methyl group, ethyl group, n-propyl group and i-propyl group are more preferable.

  In the general formula (1), examples of the hydroxyalkyl group represented by R include a hydroxymethyl group, a 1-hydroxyethyl group, a 2-hydroxyethyl group, a dihydroxyethyl group, a 1-hydroxypropyl group, a 2-hydroxypropyl group, 3-hydroxypropyl group, dihydroxypropyl group, trihydroxypropyl group, 1-hydroxybutyl group, 2-hydroxybutyl group, 3-hydroxybutyl group, 4-hydroxybutyl group, dihydroxybutyl group, trihydroxybutyl group, dihydroxybutyl Group, tetrahydroxybutyl group, pentahydroxybutyl group, 1-hydroxypentyl group, 2-hydroxypentyl group, 3-hydroxypentyl group, 4-hydroxypentyl group, 5-hydroxypentyl group, dihydroxypentyl group, trihydro Cypentyl group, tetrahydroxypentyl group, pentahydroxypentyl group, methoxymethyl group, 2-hydroxyethoxyethyl group, dihydroxypropoxymethyl group, dihydroxypropoxyethyl group, trihydroxypropoxymethyl group, trihydroxypropoxyethyl group, and 3-hydroxy A bis (2-ethoxyethyl) propyl group etc. are mentioned. Among these, from the viewpoint of adhesion between the rubber layer using the rubber composition and the metal surface, a hydroxymethyl group, a 1-hydroxyethyl group, a 2-hydroxyethyl group, a dihydroxyethyl group, a 1-hydroxypropyl group, 2 -Hydroxypropyl group, 3-hydroxypropyl group, dihydroxypropyl group, methoxymethyl group, 2-hydroxyethoxyethyl group, dihydroxypropoxymethyl group, and 3-hydroxybis (2-ethoxyethyl) propyl group are preferred, and hydroxymethyl group 1-hydroxyethyl group, 2-hydroxyethyl group, dihydroxyethyl group, methoxymethyl group, 2-hydroxyethoxyethyl group, and 3-hydroxybis (2-ethoxyethyl) propyl group are more preferable.

  Considering the above, R in the above general formula (1) may be a hydrogen atom, a methyl group, an ethyl group, an n-propyl group, i, from the viewpoint of adhesion between the rubber layer using the rubber composition and the metal surface. -Propyl group, hydroxymethyl group, 1-hydroxyethyl group, 2-hydroxyethyl group, dihydroxyethyl group, methoxymethyl group, 2-hydroxyethoxyethyl group, and 3-hydroxybis (2-ethoxyethyl) propyl group are preferred. .

  Examples of the hydroxyl group-containing compound represented by the general formula (1) include water, methanol, ethanol, propanol, isopropanol, butanol, ethylene glycol, propylene glycol, butylene glycol, pentylene glycol, diethylene glycol, triethylene glycol, and glycerin. 1,2,6-trihydroxyhexane, diglycerin, trimethylolpropane, pentaerythritol and sorbitol. As water, tap water may be sufficient and purified water, such as distilled water, ion-exchange water, and filtered water, may be sufficient. Among these, as the hydroxyl group-containing compound, water, methanol, ethanol, propanol, isopropanol, ethylene glycol, propylene glycol, diethylene glycol, triethylene glycol are used from the viewpoint of adhesion between the rubber layer using the rubber composition and the reinforcing layer. , Diglycerin, trimethylolpropane, and pentaerythritol are preferable, and water, methanol, ethanol, ethylene glycol, propylene glycol, diethylene glycol, trimethylolpropane, and pentaerythritol are more preferable. These hydroxyl group-containing compounds may be used alone or in combination of two or more.

  The content of the hydroxyl group-containing compound is 0.8 parts by mass or more and 17 parts by mass or less with respect to 100 parts by mass of the diene polymer. If the content of the hydroxyl group-containing compound is within the above range, the hydroxyl group equivalent in the rubber composition is in an appropriate range, so that a sufficient catalytic effect of the binding reaction between sulfur and the metal surface can be obtained, and the rubber composition A composition having excellent adhesion between the rubber layer used and the metal surface can be obtained. The content of the hydroxyl group-containing compound is preferably 0.85 parts by mass or more, more preferably 0.9 parts by mass or more, still more preferably 0.95 parts by mass or more with respect to 100 parts by mass of the diene polymer. 0 parts by mass or more is more preferable, 16.5 parts by mass or less is preferable, 16 parts by mass or less is more preferable, and 15.5 parts by mass or less is more preferable. 15 parts by mass or less is even more preferable. Considering the above, the content of the polyhydric alcohol compound is preferably 0.85 parts by mass or more and 16.5 parts by mass or less, and 0.9 parts by mass or more and 16 parts by mass or less with respect to 100 parts by mass of the diene polymer. Is more preferable, 0.95 to 15.5 parts by mass is more preferable, and 1.0 to 15 parts by mass is even more preferable.

[Other additives]
Moreover, the rubber composition can contain other additives as necessary within the range where the effects of the present invention are exhibited. Other additives include, for example, fillers, plasticizers, softeners, anti-aging agents, organic activators, antioxidants, antistatic agents, flame retardants, crosslinking accelerators, vulcanization retarders, ozone degradation Agents, process oils (aromatic oils) and adhesion aids.

  Examples of the filler include carbon black, silica (white carbon), clay, talc, iron oxide, zinc oxide (ZnO), titanium oxide, barium oxide, magnesium oxide, calcium carbonate, magnesium carbonate, zinc carbonate, barium sulfate, Examples include mica (mica) and diatomaceous earth. These may be used alone or in combination of two or more. As carbon black, it can select suitably according to a use and can be used. As the carbon black, ISAF class, FEF class and the like are preferable. Examples of the silica include crystalline silica, precipitated silica, amorphous silica (for example, high-temperature treated silica), fumed silica, calcined silica, precipitated silica, pulverized silica, and fused silica. In particular, silica is known to produce carbon gel (bound rubber) like carbon black, and can be suitably used as necessary. Examples of the clay include hard clay, waxite clay, kaolin clay, and calcined clay.

  Examples of the plasticizer include dioctyl phthalate (DOP), dibutyl phthalate (DBP), dioctyl adipate (DOA), isodecyl succinate, diethylene glycol dibenzoate, pentaerythritol ester, butyl oleate, methyl acetylricinoleate, tricresyl phosphate , Trioctyl phosphate, trimellitic acid ester, propylene glycol adipate polyester, butylene glycol adipate polyester, naphthene oil, and the like. These may be used alone or in combination of two or more.

  Specific examples of the softener include aroma oil, naphthene oil, paraffin oil, petroleum resin, vegetable oil, and liquid rubber. These may be used alone or in combination of two or more.

  Examples of the antioxidant include N- (1,3-dimethylbutyl) -N′-phenyl-p-phenylenediamine (6PPD), N, N′-dinaphthyl-p-phenylenediamine (DNPD), and N-isopropyl. -N'-phenyl-p-phenylenediamine (IPPD), styrenated phenol (SP), 2,2,4-trimethyl-1,2-dihydroquinoline polymer (RD), and the like. These may be used alone or in combination of two or more.

  Examples of the organic active agent include stearic acid, oleic acid, lauric acid, and zinc stearate. These may be used alone or in combination of two or more.

  Examples of the antioxidant include butylhydroxytoluene (BHT) and butylhydroxyanisole (BHA).

  Examples of the antistatic agent include quaternary ammonium salts; hydrophilic compounds such as polyglycols and ethylene oxide derivatives.

  Examples of the flame retardant include chloroalkyl phosphate, dimethyl / methylphosphonate, bromine / phosphorus compound, ammonium polyphosphate, neopentyl bromide-polyether, and brominated polyether. Examples of the non-halogen flame retardant include aluminum hydroxide, magnesium hydroxide, tricresyl phosphate, and diphenyl cresyl phosphate.

  As the crosslinking accelerating aid, general rubber auxiliaries can be used together. As the rubber auxiliary agent, for example, zinc white; stearic acid, oleic acid, and Zn salts thereof can be used.

  Examples of the vulcanization retarder include organic acids such as phthalic anhydride, benzoic acid, salicylic acid, acetylsalicylic acid; N-nitroso-diphenylamine, N-nitroso-phenyl-β-naphthylamine, N-nitroso-trimethyl-dihydroquinoline heavy Nitroso compounds such as coalescence; halides such as trichloromelanin; 2-mercaptobenzimidazole, and N- (cyclohexylthio) phthalimide (PVI). These may be used alone or in combination of two or more.

  Examples of the adhesion assistant include triazine thiol compounds (for example, 2,4,6-trimercapto-1,3,5-triazine, 6-butylamino-2,4-dimercapto-1,3,5-triazine). ), Resorcin, cresol, resorcin-formalin latex, monomethylol melamine, monomethylol urea, ethylene maleimide, cobalt naphthenate, cobalt stearate, cobalt versatate, and cobalt dodecanoate. These may be used alone or in combination of two or more.

<Method for producing rubber composition>
The rubber composition according to the present embodiment can be produced by a conventionally known production method. As a method for producing the rubber composition according to the present embodiment, for example, first, the diene polymer, if necessary, other diene polymers and polymers other than diene polymers, and the various additives described above. And so on. And the manufacturing method knead | mixed using a Banbury mixer, closed mixers, such as a kneader, kneading roll machines, such as a roll, an extruder, a twin screw extruder, etc. are mentioned.

[Rubber composition metal laminate]
The rubber composition metal laminate according to the present embodiment is a laminate of the rubber composition and a wire reinforcing layer whose surface is metal-plated. As this laminated body, a high pressure hose, a hydraulic hose, etc. are mentioned, for example. FIG. 1 is a partially broken perspective view showing an example of a hydraulic hose according to the present embodiment. As shown in FIG. 1, the hydraulic hose 1 is formed in a cylindrical shape, and includes an inner rubber layer 11 through which fluid passes, a reinforcing layer 12 provided outside the inner rubber layer 11, and an outer side of the reinforcing layer 12. And an external rubber layer 13 provided. The reinforcing layer 12 is disposed so as to be sandwiched between the inner rubber layer 11 and the outer rubber layer 13. The inner rubber layer 11, the reinforcing layer 12, and the outer rubber layer 13 are bonded and fixed by vulcanization of the inner rubber layer 11 and the outer rubber layer 13.

<Rubber layer>
As described above, the inner rubber layer 11 and / or the outer rubber layer 13 are rubber layers using the rubber composition according to the above embodiment. From the viewpoint of the weather resistance of the hose, it is preferable to form at least the outer rubber layer 13 using the rubber composition according to the above embodiment. The inner rubber layer 11 is preferably formed using a rubber composition mainly composed of acrylonitrile butadiene rubber (NBR) having excellent oil resistance.

  For example, the thickness of the internal rubber layer 11 is preferably 0.2 mm or greater and 4.0 mm or less, and more preferably 0.5 mm or greater and 2.0 mm or less. Similarly, the thickness of the external rubber layer 13 is preferably 0.2 mm or greater and 4.0 mm or less, and more preferably 0.5 mm or greater and 2.0 mm or less.

<Reinforcing layer>
The reinforcing layer 12 is a wire blade in which a steel wire is knitted, and the surface of the wire is brass-plated. This is a layer provided between the internal rubber layer 11 and the external rubber layer 13 from the viewpoint of maintaining the strength of the hydraulic hose 1. In the example shown in FIG. 1, the reinforcing layer 12 is a single layer, but a plurality of reinforcing layers 12 in which an intermediate rubber layer is disposed between the layers may be provided. In addition to the wire blade, the reinforcing layer 12 may be formed as a spiral wire in which a steel wire rod is spirally wound around the inner rubber layer 11. The material forming the reinforcing layer 12 and the knitting method, weaving method, or winding method can be appropriately selected depending on the application, for example, depending on the pressure resistance. In a hydraulic hose or the like, it is preferable to form the reinforcing layer 12 with a wire blade.

  Examples of the wire material include piano wire (carbon steel), hard steel wire, and stainless steel wire. As the wire material, piano wire (carbon steel) and hard steel wire are particularly preferable from the viewpoint of workability and strength.

  The reinforcing layer 12 is metal-plated on the surface in order to enhance the adhesion with the rubber layer. This metal plating is a piano wire and a hard steel wire coated with brass (brass). In brass coating, copper is plated on the steel wire and zinc is plated on the copper and a heat diffusion treatment is applied to form the brass coating.

<Vulcanized rubber products>
The rubber composition metal laminate of the rubber composition and the reinforcing layer 12 is crosslinked, that is, vulcanized in the presence of sulfur, so that the rubber molecules forming the inner rubber layer 11 and the outer rubber layer 13 are spaced apart from each other. Cross-linked by sulfur. By this crosslinking, elasticity and tensile strength are imparted to the inner rubber layer 11 and the outer rubber layer 13, and the metal (copper, zinc) and sulfur constituting the brass coating are bonded at the interface with the reinforcing layer 12. The inner rubber layer 11 and the outer rubber layer 13 are bonded to the reinforcing layer 12.

  Sulfur is preferably blended together with other materials when forming a compound as a rubber composition. In addition, in the blending of sulfur, molecular chains forming a diene polymer with sulfur are cross-linked by sulfur, and metal (copper, zinc) and sulfur at the interface between the inner rubber layer 11 and the outer rubber layer 13 and the reinforcing layer 12 are combined. As long as the inner rubber layer 11, the outer rubber layer 13 and the reinforcing layer 12 are bonded together by bonding to each other, it is not limited to the blending at the time of compound preparation.

  Examples of the vulcanization method include a method in which the rubber composition is heated at a predetermined temperature for a predetermined time in the presence of sulfur. The vulcanization temperature is preferably 130 ° C. or higher and 180 ° C. or lower. The vulcanization time is preferably from 30 minutes to 240 minutes. By combining the temperature and time within this range, desired physical properties of the vulcanized rubber product, such as elasticity, tensile strength, appearance, adhesion at the rubber-metal interface, and rubber attachment at the rubber-metal interface can be obtained.

  The vulcanized rubber product in the present embodiment can be suitably used as a hydraulic hose or the like. As a method for manufacturing a hydraulic hose or the like, for example, a steam vulcanization method in which a rubber composition metal laminate is enclosed in a high-pressure vessel and crosslinked in a steam can, and the rubber composition metal laminate is covered with a nylon cloth or the like. And an oven vulcanization method in which a product is vulcanized in a hot air drying furnace. In general, the steam vulcanization method is a batch process, and the oven vulcanization method is a continuous process. As a manufacturing method of the hydraulic hose, an oven vulcanization method which is a continuous process is preferable.

<Method for producing vulcanized rubber product>
Below, the manufacturing method of the vulcanized rubber product which concerns on this Embodiment is demonstrated. Here, a case where a hydraulic hose is manufactured as a vulcanized rubber product will be described as an example.

  With reference to FIG.2 and FIG.3, the manufacturing method of the hydraulic hose which concerns on this Embodiment is demonstrated. FIG. 2 is an explanatory diagram of a manufacturing process of a hydraulic hose using the rubber composition according to the embodiment of the present invention, and FIG. 3 is a diagram of the hydraulic hose using the rubber composition according to the embodiment of the present invention. It is explanatory drawing of a vulcanization | cure process.

<Hose manufacturing process>
As shown in FIG. 2, the rubber hose has a rubber material extrusion process (step S101) for forming the internal rubber layer 11, a reinforcement layer 12 knitting process (step S102), and an external rubber layer 13 extrusion / vulcanization process (step). S103) and the mandrel 101 extraction step (step S104). The manufactured rubber hose is packed and shipped through a water pressure inspection and an inspection winding process.

  First, in step S <b> 101, the unvulcanized inner rubber layer 11 is coated on the outer peripheral surface of the mandrel 101 fed from the unwinder 100 by the first extruder 102. The hose 103 covered with the internal rubber layer 11 is wound around the winding / unwinding machine 104.

  Next, in step S102, the hose 106, in which the reinforcing layer 12 is formed by braiding with the braiding machine 105 so as to cover the internal rubber layer 11 constituting the hose 103 fed out from the winding and unwinding machine 104, is unwound and unwound. Wind up on machine 107. A metal wire is used for the cord of the reinforcing layer 12. As the metal wire, a steel wire plated with brass is used in order to improve the adhesion to rubber. The reinforcing layer 12 may be formed by winding a metal wire in a spiral around the inner rubber layer 11 formed around the mandrel 101.

  Next, in step S103, the unvulcanized outer rubber layer 13 is covered by the second extruder 108 on the reinforcing layer 12 of the hose 106 fed out from the winding unwinder 107 to form the hose body 109. Then, the formed hose body 109 is wound around the winder 110. In the present embodiment, the hose 112 vulcanized by performing a vulcanization process by the vulcanizer 111 while the hose body 109 is wound around the winder 110 after leaving the second extruder 108. Although it is wound up by the winder 110, the vulcanization step may be provided after the hose body 109 is wound up by the winder 110. Further, a wrapping device 113 and an unwrapping device 114 for detaching a protective cloth such as a nylon cloth from the hose body 109 are provided before and after the vulcanizing device 111. In FIG. 2, the hose 115 before vulcanization in which the nylon cloth is wound by the wrapping device 13 becomes the hose 116 after vulcanization and before removing the nylon cloth. The vulcanization process will be described later.

  Next, in step S104, after vulcanization, the mandrel 101 is extracted from the unwrapped hose 116 unwound from the winder 110 by the mandrel extraction device 117, and the hydraulic hose 118 is completed.

<Vulcanization process>
As shown in FIG. 3, a nylon cloth 119 is wound around the hose body 109 exiting the second extruder 108 by a lapping device 113. The hose body 109 covered with the nylon cloth 119 is carried into the vulcanizer 111. The vulcanizing device 111 is a hot air circulation type continuous vulcanizing device that advances vulcanization with hot air 120. This vulcanization method is an oven vulcanization method.

  FIG. 4 is a partial cross-sectional view for explaining an example of the layer structure around the mandrel 101 to be charged into the vulcanizer. As shown in FIG. 4, an inner rubber layer 11 is formed around the mandrel 101, a reinforcing layer 12 is formed around the inner rubber layer 11, and an outer rubber layer 13 is formed around the inner rubber layer 11. A nylon cloth 119 is wound around the outer rubber layer 13 and heated in this state to proceed with the vulcanization process.

  As described above, the vulcanization temperature is preferably 130 ° C. or higher and 180 ° C. or lower, and the vulcanization time, that is, the vulcanization time in the vulcanizer 111 is preferably 30 minutes or longer and 240 minutes or shorter. In this temperature range and vulcanization time, a hydraulic hose having good adhesion between the inner rubber layer 11 and the outer rubber layer 13 and the reinforcing layer 12 is obtained. Here, by forming the inner rubber layer 11 and / or the outer rubber layer 13 using the rubber composition according to the above embodiment, the inner rubber layer 11 and / or the outer rubber layer 13 and the metal reinforcing layer 12 are formed. A hydraulic hose with good adhesiveness can be manufactured.

  In addition, according to the rubber composition, moderate moisture can be stably held in the composition until immediately before vulcanization, so even in the oven vulcanization method with large moisture evaporation, it suppresses adhesion failure and deterioration of adhesion due to lack of moisture. it can. However, it goes without saying that the rubber composition according to the above-described embodiment can be suitably used for production of rubber products by other conventionally known vulcanization methods. Examples of other vulcanization methods include press vulcanization, steam vulcanization, and hot water vulcanization.

  Moreover, in the said embodiment, although the manufacturing process by a continuous processing system was illustrated, a vulcanized rubber product can also be manufactured by the method of bonding, after manufacturing a rubber layer and a reinforcement layer by another process.

  The hydraulic hose manufactured by the manufacturing method according to the present embodiment can be applied to various uses. As a use of the hydraulic hose, for example, it can be suitably used as an air conditioner hose for automobiles, a power steering hose, a hydraulic hose used for a hydraulic system of a construction vehicle, and the like.

  Moreover, in this Embodiment, although demonstrated using the hydraulic hose as a rubber composition metal laminated body and a vulcanized rubber product, this invention is not limited to this, For example, other rubbers, such as a conveyor belt The same can be applied to the laminate.

  As described above, according to the rubber composition metal laminate, the vulcanized rubber product, and the method for producing the vulcanized rubber product, the adhesiveness between the rubber layer and the reinforcing layer is ensured even in the continuous production method by the oven vulcanization method. A good vulcanized rubber product can be provided. In particular, even when used after long-term storage in a dry state, it is possible to provide a composition that forms a rubber product having good adhesion to the reinforcing layer. This vulcanized rubber product can be suitably used for hydraulic hoses, high-pressure hoses and the like.

  Hereinafter, the present invention will be described in more detail with reference to examples made to clarify the effects of the present invention. In addition, this invention is not limited at all by the following examples and comparative examples.

<1. Preparation of rubber composition>
Example 1
Acrylonitrile-butadiene rubber (trade name “Nancar 3345”, manufactured by Nantes Chemical Co., Ltd., acrylonitrile content 34% by weight, Mooney viscosity (ML1 + 4,100 ° C.) 45) 40% by weight, ethylene-propylene-diene rubber (trade name “EPT”) 4070 ", manufactured by Mitsui Chemicals, ethylene content 56 mass%, ethylidene norbornene content 8 mass%, Mooney viscosity (ML1 + 4, 125 ° C) 47)) 30 mass%, and styrene butadiene rubber (trade name" Nipol 1502 ", 2 parts by mass with respect to 100 parts by mass of a diene polymer containing Nippon Zeon, emulsion polymerization SBR, bound styrene content 23.5% by mass, Mooney viscosity (ML1 + 4, 100 ° C.) 52) 30% by mass Sulfur (Hosoi Chemical Co., Ltd.), 1 part by weight of water, 1.7 parts by weight of sulfe Amide-based vulcanization accelerator (Nt-butylbenzothiazole-2-sulfenamide, trade name “Noxeller NS-P”, manufactured by Ouchi Shinsei Chemical Co., Ltd.) and 0.3 parts by mass of scorch inhibitor ( N-cyclohexylthiophthalimide (manufactured by FLEXSYS), 62 parts by mass of ISAF grade carbon black (trade name “Show Black N220”, manufactured by Showa Cabot), 15 parts by mass of hard clay (trade name “Suprex Clay”, Kentucky) Tennessee Clay Company, Inc.) 5 parts by mass of zinc oxide (3 types, manufactured by Shodo Chemical Industry Co., Ltd.), 1 part by mass of stearic acid (manufactured by Nippon Oil & Fats Co., Ltd.), 2.4 parts by mass of ozone degradation inhibitor ( Product name “Ozone Non 6C” (Seiko Chemical Co., Ltd.) and 10 parts by mass of plasticizer (Dioctyl Adipate, Product Name “DIACIZER DOA”, Mitsubishi Chemical) Nippon Seikagaku Co., Ltd.) and 12 parts by mass of process oil (Aroma oil, trade name “A-OMIX”, Sankyo Oil Chemical Co., Ltd.) were blended and kneaded with a Banbury Kimisar to prepare a rubber composition. The adhesiveness of the produced rubber composition was evaluated. The amount of each component is shown in Table 1 below, and the evaluation results are shown in Table 3 below.

(Example 2)
A rubber composition was prepared and evaluated in the same manner as in Example 1 except that the amount of water was 3 parts by mass. The amount of each component is shown in Table 1 below, and the evaluation results are shown in Table 3 below.

(Example 3)
A rubber composition was prepared and evaluated in the same manner as in Example 1 except that the amount of water was 6 parts by mass. The amount of each component is shown in Table 1 below, and the evaluation results are shown in Table 3 below.

Example 4
A rubber composition was produced and evaluated in the same manner as in Example 1 except that the amount of water was 15 parts by mass. The amount of each component is shown in Table 1 below, and the evaluation results are shown in Table 3 below.

(Example 5)
A rubber composition was prepared and evaluated in the same manner as in Example 1 except that 1 part by mass of ethanol was used instead of water. The amount of each component is shown in Table 1 below, and the evaluation results are shown in Table 3 below.

(Example 6)
A rubber composition was prepared and evaluated in the same manner as in Example 5 except that the amount of ethanol was 6 parts by mass. The amount of each component is shown in Table 1 below, and the evaluation results are shown in Table 3 below.

(Example 7)
A rubber composition was prepared and evaluated in the same manner as in Example 1 except that 2 parts by mass of diethylene glycol was blended in place of water. The amount of each component is shown in Table 1 below, and the evaluation results are shown in Table 3 below.

(Example 8)
A rubber composition was prepared and evaluated in the same manner as in Example 7 except that the blending amount of diethylene glycol was 3 parts by mass. The amount of each component is shown in Table 1 below, and the evaluation results are shown in Table 3 below.

Example 9
A rubber composition was prepared and evaluated in the same manner as in Example 7 except that the blending amount of diethylene glycol was 6 parts by mass. The amount of each component is shown in Table 1 below, and the evaluation results are shown in Table 3 below.

(Example 10)
A rubber composition was prepared and evaluated in the same manner as in Example 1 except that 3 parts by mass of pentaerythritol was blended in place of water. The amount of each component is shown in Table 1 below, and the evaluation results are shown in Table 3 below.

(Example 11)
A rubber composition was prepared and evaluated in the same manner as in Example 1 except that the blending amount of pentaerythritol was 15 parts by mass. The amount of each component is shown in Table 1 below, and the evaluation results are shown in Table 3 below.

(Comparative Example 1)
A rubber composition was prepared and evaluated in the same manner as in Example 1 except that water was not blended. The amount of each component is shown in Table 2 below, and the evaluation results are shown in Table 4 below.

(Comparative Example 2)
A rubber composition was prepared and evaluated in the same manner as in Example 1 except that the amount of water was 0.5 parts by mass. The amount of each component is shown in Table 2 below, and the evaluation results are shown in Table 4 below.

(Comparative Example 3)
A rubber composition was prepared and evaluated in the same manner as in Example 1 except that the amount of water was 0.75 parts by mass. The amount of each component is shown in Table 2 below, and the evaluation results are shown in Table 4 below.

(Comparative Example 4)
A rubber composition was prepared and evaluated in the same manner as in Example 1 except that the amount of water was 18 parts by mass. The amount of each component is shown in Table 2 below, and the evaluation results are shown in Table 4 below.

(Comparative Example 5)
A rubber composition was prepared and evaluated in the same manner as in Example 5 except that the amount of ethanol was 0.75 parts by mass. The amount of each component is shown in Table 2 below, and the evaluation results are shown in Table 4 below.

(Comparative Example 6)
A rubber composition was prepared and evaluated in the same manner as in Example 7 except that the blending amount of diethylene glycol was 0.75 parts by mass. The amount of each component is shown in Table 2 below, and the evaluation results are shown in Table 4 below.

(Comparative Example 7)
A rubber composition was prepared and evaluated in the same manner as in Example 10 except that the amount of pentaerythritol was 0.75 parts by mass. The amount of each component is shown in Table 2 below, and the evaluation results are shown in Table 4 below.

(Comparative Example 8)
A rubber composition was prepared and evaluated in the same manner as in Example 2 except that the amount of sulfur was 0.4 parts by mass. The amount of each component is shown in Table 2 below, and the evaluation results are shown in Table 4 below.

(Comparative Example 9)
A rubber composition was prepared and evaluated in the same manner as in Example 8 except that the amount of sulfur was 5.5 parts by mass. The amount of each component is shown in Table 2 below, and the evaluation results are shown in Table 4 below.

(Comparative Example 10)
A rubber composition was prepared and evaluated in the same manner as in Example 7 except that the amount of diethylene glycol was 18 parts by mass. The amount of each component is shown in Table 2 below, and the evaluation results are shown in Table 4 below.

(Comparative Example 11)
A rubber composition was prepared and evaluated in the same manner as in Example 10 except that the amount of pentaerythritol was 18 parts by mass. The amount of each component is shown in Table 2 below, and the evaluation results are shown in Table 4 below.

なお、表１及び表２に記載した各成分の詳細は以下のとおりである。
・ＮＢＲ：商品名「Ｎａｎｃａｒ ３３４５」、南帝化学工業社製、アクリロニトリル含有量３４質量％、ムーニー粘度（ＭＬ１＋４，１００℃）４５
・ＥＰＤＭ：商品名「ＥＰＴ ４０７０」、三井化学社製、エチレン含有量５６質量％、エチリデンノルボルネン含有量８質量％、ムーニー粘度（ＭＬ１＋４，１２５℃）４７
・ＳＢＲ：商品名「Ｎｉｐｏｌ １５０２」、日本ゼオン社製、乳化重合ＳＢＲ、結合スチレン含有量２３．５質量％、ムーニー粘度（ＭＬ１＋４，１００℃）５２
・水：水道水
・エタノール：関東化学社製
・ジエチレングリコール：日本触媒社製
・ペンタエリスリトール：日本合成化学工業社製
・硫黄：細井化学工業社製
・加硫促進剤：Ｎ−ｔ−ブチルベンゾチアゾール−２−スルフェンアミド、商品名「ノクセラーＮＳ−Ｐ」、大内新興化学工業社製
・スコーチ防止剤：Ｎ−シクロヘキシルチオフタルイミド、ＦＬＥＸＳＹＳ社製
・カーボンブラック：ＩＳＡＦ級カーボンブラック：商品名「ショウブラックＮ２２０」、昭和キャボット社製
・ハードクレー：商品名「Ｓｕｐｒｅｘ Ｃｌａｙ」、ケンタッキーテネシークレイカンパニー社製
・酸化亜鉛：酸化亜鉛３種、正同化学工業社製
・酸化マグネシウム：商品名「キョーワマグ１５０」、協和化学工業社製
・ステアリン酸：日油社製
・オゾン劣化防止剤：商品名「オゾンノン６Ｃ」、精工化学社製
・可塑剤：ジオクチルアジペート、商品名「ＤＩＡＣＩＺＥＲ ＤＯＡ」、三菱化成ビニル社製
・プロセスオイル：アロマ系オイル、商品名「Ａ−ＯＭＩＸ」、三共油化工業社製

In addition, the detail of each component described in Table 1 and Table 2 is as follows.
NBR: trade name “Nancar 3345”, manufactured by Nanteru Chemical Industry Co., Ltd., acrylonitrile content: 34% by mass, Mooney viscosity (ML1 + 4, 100 ° C.) 45
EPDM: Trade name “EPT 4070”, manufactured by Mitsui Chemicals, ethylene content 56 mass%, ethylidene norbornene content 8 mass%, Mooney viscosity (ML1 + 4, 125 ° C.) 47
SBR: trade name “Nipol 1502”, manufactured by Nippon Zeon Co., Ltd., emulsion polymerization SBR, bound styrene content 23.5 mass%, Mooney viscosity (ML1 + 4, 100 ° C.) 52
Water: tap water Ethanol: manufactured by Kanto Chemical Co., Ltd. Diethylene glycol: manufactured by Nippon Shokubai Co., Ltd. Pentaerythritol: manufactured by Nippon Synthetic Chemical Industry Co., Ltd. Sulfur: manufactured by Hosoi Chemical Co., Ltd. Vulcanization accelerator: Nt-butylbenzothiazole -2-sulfenamide, trade name “Noxeller NS-P”, manufactured by Ouchi Shinsei Chemical Co., Ltd., scorch inhibitor: N-cyclohexylthiophthalimide, manufactured by FLEXSYS Corporation, carbon black: ISAF grade carbon black: trade name “Show” Black N220 ", Showa Cabot Co., Ltd., hard clay: Trade name" Suprex Clay ", Kentucky Tennessee Clay Company Co., Ltd., zinc oxide: Zinc oxide, Zinc Oxide Corporation, Magnesium oxide: Trade name" Kyowa Mag 150 " , Manufactured by Kyowa Chemical Industry Co., Ltd., stearic acid: manufactured by NOF Corporation, prevention of ozone deterioration Stopper: Trade name “Ozone Non 6C”, Seiko Chemical Co., Ltd., Plasticizer: Dioctyl Adipate, Trade name “DIACIZER DOA”, Mitsubishi Kasei Vinyl, Process oil: Aroma oil, Trade name “A-OMIX”, Sankyo Made by Yuka Industries Co., Ltd.

<2. Evaluation of rubber composition>
Each of the rubber compositions obtained in Examples 1 to 11 and Comparative Examples 1 to 11 is a hose-like test piece having a rubber outer layer made of each rubber composition and a reinforcing layer made of brass-plated wire. As shown in FIG.

  First, a reinforcing layer was formed by winding a brass plating wire in a blade shape on a mandrel having an outer diameter of 34 mm. Next, an unvulcanized hose-shaped test piece was obtained by laminating an unvulcanized sheet having a thickness of 2.5 mm prepared from each of the obtained rubber compositions on the reinforcing layer. Next, a curing tape (protective cloth) made of nylon 66 was wrapped so as to cover the outside of the unvulcanized hose-like test piece and vulcanized.

Vulcanization was carried out under the following two conditions, and the hose-like vulcanized test piece obtained was evaluated for adhesion strength and with rubber. In addition, adhesive strength and with rubber | gum are the average values of the value measured 10 times, respectively.
-Vulcanization condition 1: An unvulcanized hose-like specimen prepared using the rubber composition immediately after kneading was vulcanized for 90 minutes in a steam can at 142 ° C (steam vulcanization).
-Vulcanization condition 2: An unvulcanized hose-like specimen prepared using the rubber composition immediately after kneading was vulcanized in an atmospheric oven at 142 ° C for 135 minutes (oven vulcanization).

  With respect to each hose-like vulcanized test piece obtained under the above-described vulcanizing condition 1 and vulcanizing condition 2, the adhesive strength (kN / m) and the rubber attached (%) were evaluated. Here, the adhesive strength (kN / m) is the magnitude of force per unit width (m) required for peeling the outer rubber layer from the interface between the outer rubber layer and the reinforcing layer at a peeling speed of 50 mm / min ( kN). Here, the term “with rubber” refers to the ratio of the outer rubber layer of the hose-like vulcanized test piece remaining on the surface of the reinforcing layer and the area ratio of the remaining rubber layer to the entire surface area of the reinforcing layer expressed as a percentage. is there. The values of adhesive strength (kN / m) and with rubber (%) are average values measured 10 times. The evaluation results are shown in Tables 3 and 4. In Tables 3 and 4, adhesive evaluation 1 is an evaluation of a hose-like vulcanized test piece vulcanized under vulcanization condition 1, and adhesive evaluation 2 is vulcanized under vulcanization condition 2. This is an evaluation of a hose-like vulcanized test piece. It can be said that the adhesiveness is good when the value of the adhesive strength is 2.5 kN / m or more and the rubber attachment is 60% or more.

Furthermore, the external appearance of the outer rubber layer was visually evaluated on the following criteria for each hose-like vulcanized test piece.
○: No dent defect (porous) ×: dent defect (porous) −: Not measured

  As can be seen from Table 3 and Table 4, in Example 1-11 in which the hydroxyl group equivalent compound was blended with the diene polymer so that the hydroxyl equivalent was a predetermined amount, the steam vulcanization method and the oven vulcanization method were used. It turns out that the outstanding adhesiveness is acquired in any case. On the other hand, when a hydroxyl-containing compound is not mix | blended, it turns out that the adhesive evaluation on oven vulcanization conditions deteriorates remarkably (Comparative Examples 1-3 and 5-7). Furthermore, when the hydroxyl group equivalent of the polyhydric alcohol compound is larger than the predetermined range, it can be seen that sufficient adhesion evaluation can be obtained even by the oven vulcanization method, while the rubber appearance is remarkably deteriorated (Comparative Examples 4, 10, 11). ). These results are considered because the balance of the catalytic function of the binding reaction between sulfur and the metal surface by the hydroxyl group-containing compound was deteriorated. Moreover, when sulfur is more than a predetermined range, it turns out that adhesion evaluation tends to be lowered in any vulcanization method (Comparative Example 9). When sulfur is less than a predetermined range, the adhesive strength is remarkably high. It turns out that it gets worse (Comparative Example 8). These results are considered because the balance of the catalytic function of the binding reaction between sulfur and the metal surface by the hydroxyl group-containing compound was deteriorated.

DESCRIPTION OF SYMBOLS 1 Hydraulic hose 11 Internal rubber layer 12 Reinforcement layer 13 External rubber layer 100 Unwinder 101 Mandrel 102 1st extruder 103 Hose 104 Winding unwinding machine 105 Braiding machine 106 Hose 107 Unwinding unwinding machine 108 2nd extruder 109 Hose body 110 Winder 111 Vulcanization device 112 Hose 113 Lapping device 114 Unwrapping device 115 Hose 116 Hose 117 Mandrel extraction device 118 Hydraulic hose 119 Nylon cloth 120 Hot air

Claims (8)

100 parts by weight of a diene polymer that can be vulcanized with sulfur,
0.5 parts by mass or more and 5 parts by mass or less of sulfur;
A hydroxyl group-containing compound having a molecular weight of not more than 0.8 parts by weight and not more than 17 parts by weight of 200 or less;
A rubber composition comprising: The rubber composition according to claim 1, wherein the hydroxyl group-containing compound is represented by the following general formula (1).
ROH (1)
(In the formula (1), R represents a hydrogen atom, an ether bond, and an alkyl group having 1 to 5 carbon atoms which may contain a branch or an ether bond and a branch having 1 to 10 carbon atoms which may contain an branch. Hereinafter, it represents a hydroxyalkyl group having a hydroxyl group of 5 or less.)   The rubber composition metal laminated body provided with the reinforcement layer which has a metal surface, and the rubber layer containing the rubber composition of Claim 1 or Claim 2 provided on the said metal surface.   The rubber composition metal laminate according to claim 3, wherein the metal surface is brass-plated.   The rubber composition metal laminate according to claim 3 or 4, wherein the reinforcing layer has a braided structure in which wires are knitted or a spiral structure.   A vulcanized rubber product obtained by using the rubber composition according to claim 1.   A vulcanized rubber product in which the rubber layer of the rubber composition metal laminate according to any one of claims 3 to 5 is vulcanized in the presence of sulfur and bonded to the reinforcing layer.   The vulcanized rubber product according to claim 7, which is a hose.

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