Patent Application
20150000781
The present technology relates to a rubber/resin composite hose.
Conventionally, a resin and rubber laminate that is a combination of a resin material and a rubber material is normally used in hose for the transport of liquids, as typified by hose for liquid propane gas (LPG hose) or car air conditioner hose, and, normally, a method of bonding between the resin and the rubber uses an adhesive, or a surface treatment of the resin material is carried out. However, in order to obtain good adhesion conditions, it is necessary to carry out these processes under defined conditions, so not only does the number of work processes increase, but there is also the problem of production cost, and the like. Therefore, the applicant of the present application has proposed fusion bonding between ultrahigh molecular weight polyethylene (PE) and rubber (fusion bonding that occurs by intertwining the molecular chains of both materials by heating to above the melting point of ultrahigh molecular weight PE) (see Japanese Examined Patent No. H07-117179). Also, bonding of polyamide resin and rubber has been proposed (see Japanese Patent Nos. 3891718, 2589238, and 3381398). Also, the applicant of the present application has previously proposed bonding between polyamide resin and rubber in Japanese Unexamined Patent Application Publication No. 2002-079614.
However, in each case, the bonding technology is between limited materials, so a technology that can be applied to bonding a wider range of resin materials and rubber materials is required.
The present technology provides a rubber/resin composite hose that has excellent adhesion properties between a resin layer and a rubber layer.
As a result of diligent research by the inventors, it was found that a rubber/resin composite hose that includes an inner tube, the inner tube having a resin layer as an innermost layer; and a rubber layer adjacent to the innermost layer, in which a material used in the resin layer is a resin composition that includes a resin including at least an ionomer containing a metal carboxylate, and a material used in the rubber layer is a rubber composition that includes a rubber including at least an epoxidized rubber, has excellent adhesion between the resin layer and the rubber layer, and the present technology was completed.
Specifically, the present technology provides the following 1 to 13.
1. A rubber/resin composite hose comprising: an inner tube, and the inner tube including a resin layer as an innermost layer and a rubber layer adjacent to the innermost layer;
a material used in the resin layer being a resin composition that includes a resin including at least an ionomer containing a metal carboxylate,
a material used in the rubber layer being a rubber composition that includes a rubber including at least an epoxidized rubber.
2. The rubber/resin composite hose according to 1 above, wherein a quantity of the ionomer in the resin is from 10 to 100 mass % of a total quantity of the resin, and
a quantity of the epoxidized rubber in the rubber is from 10 to 100 mass % of a total quantity of the rubber.
3. The rubber/resin composite hose according to 1 or 2 above, wherein the epoxidized rubber is an epoxidized natural rubber.
4. The rubber/resin composite hose according to any of 1 to 3 above, wherein an epoxidization rate of the epoxidized rubber is from 2 to 75 mol %.
5. The rubber/resin composite hose according to any of 1 to 4 above, wherein the rubber further includes an acrylonitrile butadiene rubber (NBR).
6. The rubber/resin composite hose according to any of 1 to 5 above, wherein the resin further includes a polyamide.
7. The rubber/resin composite hose according to 6 above, wherein the polyamide is at least one selected from the group consisting of polyamide 6, polyamide 11, polyamide 12, polyamide 4-6, polyamide 6-6, polyamide 6-10, polyamide 6-12, and polyamide MXD-6.
8. The rubber/resin composite hose according to any of 1 to 7 above, wherein the rubber composition further includes a thiuram vulcanization accelerator and/or a sulfenamide vulcanization accelerator, and an alkylphenol-formaldehyde resin.
9. The rubber/resin composite hose according to any of 1 to 8 above, wherein there is no adhesive layer between the resin layer and the rubber layer.
10. The rubber/resin composite hose according to any of 1 to 9 above, wherein the resin layer and the rubber layer are directly bonded.
11. The rubber/resin composite hose according to any of 1 to 10 above, wherein a reinforcing layer and an outer layer are provided on an outer side of the inner tube.
12. The rubber/resin composite hose according to 11 above, wherein a material used in the reinforcing layer is a brass-plated wire.
13. A method of manufacturing a rubber/resin composite hose, comprising: manufacturing the rubber/resin composite hose described in any of 1 to 12 above, by at least vulcanization bonding between the resin layer and the rubber layer.
The rubber/resin composite hose according to the present technology has excellent adhesion properties between the resin layer and the rubber layer.
The rubber/resin composite hose obtained by the method of manufacturing a rubber/resin composite hose according to the present technology has excellent adhesion properties between the resin layer and the rubber layer.
The present technology is described in detail below.
A rubber/resin composite hose according to the present technology includes an inner tube, the inner tube having a resin layer as an innermost layer and a rubber layer adjacent to the innermost layer. In such a rubber/resin composite hose, a material used in the resin layer is a resin composition that includes a resin including at least an ionomer containing a metal carboxylate, and a material used in the rubber layer is a rubber composition that includes a rubber including at least an epoxidized rubber, thereby forming a rubber/resin composite hose.
The material used in the resin layer of the rubber/resin composite hose according to the present technology is a resin composition that includes a resin including at least an ionomer containing a metal carboxylate, and the material used in the rubber layer is a rubber composition that includes a rubber including at least an epoxidized rubber, so it is possible to bond between the resin layer and the rubber layer, and the adhesion properties between the resin layer and the rubber layer are excellent. Also, it is possible to directly bond between the resin layer and the rubber layer without an adhesion process (for example, applying adhesive, surface treatment of the resin layer) between the resin layer and the rubber layer.
The inventors of the present application consider that the adhesion between the resin layer and the rubber layer is due to the reaction between the metal carboxylate and the epoxy group of the epoxidized rubber. The above mechanism is an inference by the inventors of the present application, but if the mechanism of the technology of the present application is a mechanism other than that described above, it is still within the scope of the present technology.
The rubber/resin composite hose according to the present technology includes the inner tube. Also, the inner tube includes the resin layer as the innermost layer and the rubber layer adjacent to the innermost layer.
In a preferred form of the rubber/resin composite hose according to the present technology, a reinforcing layer and an outer layer are provided on an outer side of the inner tube. The reinforcing layer can be adjacent to the rubber layer.
In the rubber/resin composite hose according to the present technology, the resin layer and the rubber layer can be directly bonded.
In the present technology, direct bonding of the resin layer and the rubber layer is a preferred form from the point of view of reduction of manufacturing processes and excellent productivity.
In the present technology, not having an adhesive layer between the resin layer and the rubber layer is a preferred form from the point of view of reduction of manufacturing processes and excellent working environment and productivity.
Also, in the present technology, not applying a surface treatment agent to a surface of the resin layer is a preferred form from the point of view of reduction of manufacturing processes and excellent productivity.
The thickness of the innermost layer (resin layer) is preferably from 0.05 to 1.00 mm, from the point of view of flexibility of the hose and productivity.
The thickness of the rubber layer is preferably from 0.5 to 6.0 mm from the point of view of flexibility of the hose and productivity.
The thickness of the inner tube is preferably from 0.6 to 7.0 mm.
The thickness of the outer layer is preferably from 1.0 to 4.0 mm, from the point of view of flexibility of the hose and productivity.
An example of a preferred embodiment of a rubber/resin composite hose of the present technology is described below while referencing the attached drawing. However, the present technology is not limited to the attached drawing.
In
A description of the innermost layer is given below.
In the present technology, the innermost layer is the resin layer. Also, a material used in the resin layer is a resin composition that includes a resin including at least an ionomer containing a metal carboxylate.
Because the innermost layer in the present technology is the resin layer, the present technology has excellent impermeability to liquids and gases and oil resistance.
The following is a description of the resin composition used when manufacturing the innermost layer.
In the present technology, the resin composition used is a composition that includes a resin including at least an ionomer containing a metal carboxylate.
The following is a description of the ionomer.
The ionomer that is at least included in the resin included in the resin composition is not limited in particular, provided it is a polymer containing a metal carboxylate.
The metal of the metal carboxylate in the ionomer is, for example, sodium, zinc, or magnesium. Of these, zinc is preferable from the point of view of more excellent adhesion between the resin layer and the rubber layer.
The ionomer may be a resin in which, for example, an ethylene-methacrylate copolymer is cross-linked between molecules with a metal ion (for example, zinc ion).
A method of producing the ionomer is not particularly limited. Examples thereof include conventionally known products. A single ionomer can be used or a combination of two or more ionomers can be used.
In the present technology, the resin includes at least the ionomer.
A polymer other than the ionomer that can be included in the resin include, for example, a polyamide, and a polyolefin.
Of these, preferably, the resin further includes a polyamide from the point of view of excellent impermeability to gases, oil resistance, and mechanical strength.
The polyamide is preferably at least one selected from the group consisting of polyamide 6, polyamide 11, polyamide 12, polyamide 4-6, polyamide 6-6, polyamide 6-10, polyamide 6-12, polyamide MXD-6, from the point of view of more excellent impermeability to gases, oil resistance, and mechanical strength.
There is no particular limitation on the manufacture of the polymer other than the ionomer. Examples thereof include conventionally known products. A single or a combination of two or more types can be used as the polymer other than the ionomer.
In the resin, preferably, a content of the ionomer is from 10 to 100 mass %, and more preferably from 20 to 100 mass % of the total quantity of the resin, from the contribution of the ionomer content to the adhesion properties.
If the resin includes the polymer other than the ionomer, the quantity of the polymer (for example, polyamide) other than the ionomer can be 90 mass % or less of the total quantity of the resin. Preferably, the quantity of the polymer other than the ionomer is from 10 to 90 mass %, and more preferably from 40 to 90 mass % of the total quantity of the resin, from the point of view of improving impermeability to gases, oil resistance, and mechanical strength.
The resin composition can include additives as desired, as long as the object of the present technology is not hindered. Examples of the additives include fillers, reinforcing agents, anti-aging agents, vulcanizing agents, vulcanization accelerators, vulcanization activators, plasticizers, pigments (dyes), tackifiers, lubricants, dispersing agents, and processing aids.
A manufacturing method of the resin composition is not particularly limited. For example, a method in which an ionomer, a polymer other than an ionomer which can be used if necessary, and additives are mixed using a biaxial mixing extruder can be used. A preferred form is to use a mixing temperature that is not less than or close to the melting point of the resin.
A description of the rubber layer is given below.
In the present technology, the rubber layer is adjacent to the innermost layer. The material used in the rubber layer is a rubber composition that includes a rubber including at least an epoxidized rubber.
A description of the rubber composition used when manufacturing the rubber layer is given below.
In the present technology, there is no particular limitation on the epoxidized rubber included in the rubber included in the rubber composition, provided it is rubber that has an epoxy group. Preferably, the epoxidized rubber is an epoxidized natural rubber from the point of view of more excellent adhesion properties between the resin layer and the rubber layer.
Because the epoxy group in the epoxidized rubber contributes to the adhesion between the resin layer and the rubber layer, preferably, an epoxidization rate is from 2 to 75 mol %, and more preferably from 20 to 75 mol %. The epoxidization rate means the percentage of the total number of double bonds in the raw material rubber (for example, natural rubber) before epoxidization that have been epoxidized.
There is no particular limitation on the manufacture of the epoxidized rubber. Examples thereof include conventionally known products. A single epoxidized rubber can be used or a combination of two or more types can be used.
In the present technology, the rubber includes at least the epoxidized rubber.
Examples of the rubber other than the epoxidized rubber that can be included in the rubber include acrylonitrile-butadiene rubber (NBR), natural rubber (NR), butadiene rubber (BR), styrene-butadiene copolymer rubber (SBR), polyisoprene rubber (IR), butyl rubber (IIR), chlorobutyl rubber (Cl-IIR), bromobutyl rubber (Br-IIR), chloroprene rubber, ethylene-propylene copolymer rubber, styrene-isoprene copolymer rubber, styrene-isoprene-butadiene copolymer rubber, isoprene-butadiene copolymer rubber, and chlorosulfonated polyethylene.
Preferably, the acrylonitrile-butadiene rubber (NBR) is further included in the rubber, from the point of view of more excellent adhesion properties between the resin layer and the rubber layer, and excellent oil resistance.
There is no particular limitation on the manufacture of the rubber other than the epoxidized rubber. Examples thereof include conventionally known products. A single rubber other than the epoxidized rubber can be used or a combination of two or more types can be used.
Preferably, the quantity of the epoxidized rubber in the rubber is from 10 to 100 mass % of the total quantity of the rubber, for more excellent adhesion between the resin layer and the rubber layer, and more preferably from 20 to 70 mass % taking into consideration various properties such as low temperature resistance.
If the rubber other than the epoxidized rubber is included in the rubber, the quantity of the rubber (for example, acrylonitrile-butadiene rubber) other than the epoxidized rubber can be 90 mass % or less of the total quantity of the rubber. Preferably, the quantity of the rubber other than the epoxidized rubber is from 30 to 90 mass %, and more preferably is 50 to 90 mass % of the total quantity of the rubber, from the point of view of more excellent adhesion between the resin layer and the rubber layer, and excellent oil resistance.
In the present technology, preferably, a thiuram vulcanization accelerator and/or a sulfenamide vulcanization accelerator is further included in the rubber composition, from the point of view of more excellent adhesion between the resin layer and the rubber layer, excellent vulcanized adhesion between the rubber layer and the reinforcing layer, and excellent adhesion between the rubber layer and the reinforcing layer. Also, preferably, an alkylphenol-formaldehyde resin is further included in the rubber composition, from the point of view of more excellent adhesion between the resin layer and the rubber layer, excellent vulcanized adhesion between the rubber layer and the reinforcing layer, and excellent adhesion between the rubber layer and the reinforcing layer. Preferably, a thiuram vulcanization accelerator and/or a sulfenamide vulcanization accelerator and an alkylphenol-formaldehyde resin is further included in the rubber composition, from the point of view of more excellent adhesion between the resin layer and the rubber layer, excellent vulcanized adhesion between the rubber layer and the reinforcing layer, and excellent adhesion between the rubber layer and the reinforcing layer.
In the present technology, by further including a thiuram vulcanization accelerator and/or a sulfenamide vulcanization accelerator and an alkylphenol-formaldehyde resin in the rubber composition, more excellent adhesion between the resin layer and the rubber layer, and stronger direct bonding between the rubber layer and the reinforcing layer can be obtained.
Also, by further including a thiuram vulcanization accelerator and/or a sulfenamide vulcanization accelerator in the rubber composition (in particular, by including a sulfenamide accelerator), the adhesion between the resin layer and the rubber layer under high temperatures (for example, from 40 to 120° C., and 70° C. is a preferred form) can be equal to or better than the adhesion between the resin layer and the rubber layer when current adhesives (for example, phenolic resin adhesives) are used.
In the present technology, direct bonding of the rubber layer and the reinforcing layer is a preferred form from the point of view of reduction of manufacturing processes and excellent productivity.
Also, not having an adhesive layer between the rubber layer and the reinforcing layer is a preferred form from the point of view of reduction of manufacturing processes and excellent working environment and productivity.
The following is a description of the thiuram vulcanization accelerator.
In the present technology, there is no particular limitation on the thiuram vulcanization accelerator that can be further included in the rubber composition, provided that it is a thiuram vulcanization accelerator that is commonly blended into rubber. For example, the thiuram vulcanization accelerator represented by the following Formula (1) can be used.
In the above formula (1), R1 to R4 represent an aliphatic hydrocarbon group, an alicyclic hydrocarbon group, or an aromatic hydrocarbon group, each having from 1 to 18 carbons, and x represents an integer from 1 to 4.
The aliphatic hydrocarbon group can be, for example, a straight chain alkyl group such as a methyl group, an ethyl group, a propyl group, a butyl group, a pentyl group, an octyl group, a dodecyl group, and a stearyl group; a branched alkyl group such as an isopropyl group, an isobutyl group, an s-butyl group, a t-butyl group, an isopentyl group, a neopentyl group, a t-pentyl group, a 1-methy butyl group, a 1-methyl heptyl group, and a 2-ethyl hexyl group; an alkenyl group such as a vinyl group, an aryl group, a propenyl group, a but-2-en-1-yl (—CH2—CH═CH—CH3), and a but-3-en-1-yl (—CH2—CH2—CH═CH2); or an alkynyl group such as an ethynyl group, a propynyl group, but-2-yn-1-yl (—CH2—C≡C—CH3), and a but-3-yn-1-yl (—CH2—CH2—C≡CH).
The alicyclic hydrocarbon group can be, for example, a cyclohexyl group, a methyl cyclohexyl group, or an ethyl cyclohexyl group.
The aromatic hydrocarbon group can be, for example, an aralkyl group such as a benzyl group, and a phenethyl group; or an aryl group such as a phenyl group, a tolyl group (o-, m-, p-), a dimethylphenyl group, and a mesityl group.
Specific examples of the thiuram vulcanization accelerator include tetramethyl thiuram monosulfide; or thiuram disulfide such as tetraethylthiuram disulfide, tetrabutylthiuram disulfide, tetrahexylthiuram disulfide, tetrakis(2-ethylhexyl)thiuram disulfide, tetrastearyl thiuram disulfide, tetracyclohexyl thiuram disulfide, and tetrabenzyl thiuram disulfide.
Of these, tetramethyl thiuram monosulfide, tetraethylthiuram disulfide, and tetrakis(2-ethylhexyl)thiuram disulfide, and the like are preferred from the point of view of more excellent adhesion between the resin layer and the rubber layer, excellent vulcanized adhesion between the rubber layer and the reinforcing layer, and excellent rubber properties.
A single thiuram vulcanization accelerator can be used or a combination of two or more thiuram vulcanization accelerators can be used. A method of producing the thiuram vulcanization accelerator is not particularly limited. Examples thereof include conventionally known methods.
Preferably, the quantity of thiuram vulcanization accelerator is from 0.2 to 3.0 parts by mass, more preferably from 0.25 to 2.75 parts by mass, and most preferably from 0.3 to 2.5 parts by mass, per 100 parts by mass of the rubber including the epoxidized rubber, from the point of view of more excellent adhesion between the resin layer and the rubber layer, excellent vulcanized adhesion between the rubber layer and the reinforcing layer, and excellent adhesion between the rubber layer and the reinforcing layer.
If the quantity of thiuram vulcanization accelerator is 0.2 parts or greater by mass per 100 parts by mass of the rubber including the epoxidized rubber, the adhesion properties of the reinforcing layer (in particular, brass-plated steel wire) are excellent (specifically, the adhesion force is high and the amount of rubber attachment is large), and this is desirable.
If the quantity of the thiuram vulcanization accelerator is 3.0 parts or less by mass per 100 parts by mass of the rubber including the epoxidized rubber, the scorch time becomes suitably long, the extrusion processability becomes excellent, and this is desirable.
The following is a description of the sulfenamide vulcanization accelerator.
In the present technology, there is no particular limitation on the sulfenamide vulcanization accelerator that can be included in the rubber composition, provided that it is a sulfenamide vulcanization accelerator that is commonly blended into rubber.
The sulfenamide vulcanization accelerator may be, for example, N-cyclohexyl-2-benzothiazolyl sulfenamide, or N-tert-butyl-2-benzothiazolyl sulfenamide.
Of these, N-t-butyl-2-benzothiazolyl sulfenamide is preferable from the point of view of more excellent adhesion between the resin layer and the rubber layer, excellent vulcanized adhesion between the rubber layer and the reinforcing layer, and excellent adhesion properties between the rubber layer and the reinforcing layer.
A single sulfenamide vulcanization accelerator can be used or a combination of two or more sulfenamide vulcanization accelerators can be used. A method of producing the sulfenamide vulcanization accelerator is not particularly limited. Examples thereof include conventionally known methods.
Preferably, the quantity of the sulfenamide vulcanization accelerator is from 0.5 to 5.0 parts by mass, more preferably from 0.6 to 4.0 parts by mass, and most preferably from 0.7 to 3.0 parts by mass, per 100 parts by mass of the rubber including the epoxidized rubber, from the point of view of more excellent adhesion between the resin layer and the rubber layer, excellent vulcanized adhesion between the rubber layer and the reinforcing layer, and excellent adhesion between the rubber layer and the reinforcing layer.
If the quantity of the sulfenamide vulcanization accelerator is 0.5 parts or greater by mass per 100 parts by mass of the rubber including the epoxidized rubber, the adhesion properties of the reinforcing layer (in particular, brass-plated steel wire) are excellent (specifically, the adhesion force is high and the amount of rubber attachment is large), the necessary properties can be exhibited, and this is desirable.
If the quantity of the sulfenamide vulcanization accelerator is 5.0 parts or less by mass per 100 parts by mass of the rubber including the epoxidized rubber, the scorch time becomes suitably long, the extrusion processability and applicability become excellent, and this is desirable.
The alkylphenol-formaldehyde resin is described below.
In the present technology, there is no particular limitation on the alkylphenol-formaldehyde resin that can be further included in the rubber composition, provided that it is a alkylphenol-formaldehyde resin that is commonly blended with rubber as a vulcanizing agent. Examples thereof include conventionally known products.
Of these, from the point of view of more excellent adhesion between the resin layer and the rubber layer, excellent vulcanized adhesion between the rubber layer and the reinforcing layer, and excellent adhesion between the rubber layer and the reinforcing layer, a halogenated alkylphenol-formaldehyde resin is preferable, and a brominated alkylphenol-formaldehyde resin is more preferable.
A single alkylphenol-formaldehyde resin can be used or a combination of two or more alkylphenol-formaldehyde resins can be used. A method of manufacturing the alkylphenol-formaldehyde resin is not particularly limited. Examples thereof include conventionally known methods.
Preferably, the quantity of the alkylphenol-formaldehyde resin is from 1 to 10 parts by mass, more preferably from 2 to 8 parts by mass, and most preferably from 3 to 7 parts by mass, per 100 parts by mass of the rubber including the epoxidized rubber, from the point of view of more excellent adhesion between the resin layer and the rubber layer, excellent vulcanized adhesion between the rubber layer and the reinforcing layer, and excellent adhesion between the rubber layer and the reinforcing layer.
If the quantity of the alkylphenol-formaldehyde resin is 1 part or greater by mass per 100 parts by mass of the rubber including the epoxidized rubber, the adhesion properties of the reinforcing layer (in particular, brass-plated steel wire) are excellent (specifically, the adhesion force is high and the amount of rubber attachment is large), and this is desirable.
If the quantity of the alkylphenol-formaldehyde resin is 10 parts or less by mass per 100 parts by mass of the rubber including the epoxidized rubber, the hardness of the rubber becomes appropriate, the scorch time becomes suitably long, the extrusion processability and applicability become excellent, and this is desirable.
In the present technology, the rubber composition can include a sulfur as a vulcanizing agent. The sulfur that can be further included in the rubber composition is not particularly limited. Examples thereof include conventionally known products. Specific examples include a powdered sulfur, a precipitated sulfur, a colloidal sulfur, a surface treated sulfur, and an insoluble sulfur.
A single sulfur may be used alone or a combination of two or more sulfurs may be used.
The quantity of the sulfur is preferably from 1.5 to 3.0 parts by mass, and more preferably from 1.7 to 2.5 parts by mass, per 100 parts by mass in the rubber including the epoxidized rubber, from the point of view of good tensile properties after vulcanization (for example, tensile stress at 100% elongation, tensile strength, and the like) and heat aging resistance.
The rubber composition can include additives as desired, as long as the object of the present technology is not hindered. The additives can include, for example, fillers, reinforcing agents, anti-aging agents, vulcanizing agents other than the sulfur, vulcanization accelerators other than the thiuram vulcanization accelerator and the sulfenamide vulcanization accelerator (for example, dibenzothiazyl disulfide), resins other than the alkylphenol-formaldehyde resin, vulcanization activating agents, plasticizers, pigments (dyes), tackifying agents, lubricants, dispersing agents, and process enhancing agents.
In the present technology, a manufacturing method of the rubber composition is not particularly limited. Examples thereof include a method wherein the rubber and the thiuram vulcanization accelerator, the sulfenamide vulcanization accelerator, the alkylphenol-formaldehyde resin, the sulfur, and the additives, which can be used as necessary, are mixed (kneaded) using an open roll, a kneader, an extruder, a universal blender, or a batch kneader.
A description of the reinforcing layer is given below.
The rubber/resin composite hose of the present technology can maintain strength and have excellent pressure resistance by having the reinforcing layer.
A material for the reinforcing layer that can be included in the rubber/resin composite hose of the present technology is not particularly limited.
Examples of the material used in the reinforcing layer include, for example, fiber materials such as a polyester-based fiber, a polyamide-based fiber, an aramid fiber, vinylon fiber, a rayon fiber, a poly-p-phenylene-benzobisoxazole (PBO) fiber, a polyketone fiber, and a polyarylate fiber; and metal materials such as a hard steel wire (e.g. a brass-plated wire, a zinc-plated wire, and the like), and the like.
Of these, for hose that is required to be high pressure resistant, a brass-plated wire is preferable from the point of view of excellent vulcanized adhesion between the rubber layer and the reinforcing layer, and excellent adhesion properties between the rubber layer and the reinforcing layer.
There is no limitation on the brass-plated wire, provided it is used for reinforcing a rubber hose.
A shape of the reinforcing layer is not particularly limited. Examples thereof include a braid wind shape and a spiral wind shape.
A single material for the reinforcing layer can be used or a combination of two or more materials for the reinforcing layer can be used.
If the reinforcing layer is the brass-plated wire, preferably, the rubber composition further includes a thiuram vulcanization accelerator and/or a sulfenamide vulcanization accelerator, and an alkylphenol-formaldehyde resin, from the point of view of enabling the adhesion to the brass-plated wire, while maintaining the adhesion to the resin layer.
A description of the outer layer is given below.
The rubber/resin composite hose of the present technology can protect the reinforcing layer and have excellent durability by having the outer layer.
A preferred form of the outer layer that can be included in the rubber/resin composite hose of the present technology is a rubber layer.
A material for the outer layer that can be included in the rubber/resin composite hose of the present technology is not particularly limited. Examples of the material used for the outer layer include other rubber compositions, as well as the rubber composition used in the present technology.
There is no particular limitation on the rubber included in the rubber composition used in forming the outer layer. Examples include styrene butadiene rubber (SBR), acrylonitrile butadiene rubber (NBR), butyl rubber (IIR), ethylene propylene diene rubber (EPDM), hydrogenated NBR (HNBR), chloroprene rubber (CR), chlorosulfonated methyl polyethylene (CSM), chlorinated polyethylene (CM), brominated butyl rubber (BIIR), chlorinated butyl rubber (CIIR), and BIMS.
There is no particular limitation on the manufacture of the rubber/resin composite hose of the present technology. For example, a method that uses at least vulcanized adhesion between the resin layer and the rubber layer can be used. More specifically, for example, a method in which the resin layer, the rubber layer, the reinforcing layer, and the outer layer are laminated in that order on a mandrel and, thereafter, these layers are bonded by vulcanizing can be used. Also, in the present technology, it is possible to directly bond the resin layer and the rubber layer without an adhesive process (for example, applying adhesive, surface treatment of the resin layer) between the resin layer and the rubber layer.
The temperature when vulcanizing is preferably from 140 to 190° C., from the point of view of the adhesion properties between the resin layer and the rubber layer and exhibiting the rubber properties.
The vulcanization time is preferably from 30 to 180 minutes, from the point of view of the adhesion properties between the resin layer and the rubber layer, rubber properties, and energy efficiency.
Examples of vulcanization methods include press vulcanization, steam vulcanization, oven vulcanization (hot air vulcanization), and hot water vulcanization.
In the rubber/resin composite hose of the present technology, preferably, the adhesion strength between the resin layer and the rubber layer is 50 N/25 mm or greater.
In the present technology, the adhesion strength between the resin layer and the rubber layer is the value obtained by measuring the adhesion strength (units=N/25 mm width) in a peeling test. In the peeling test, a resin sheet (sheet thickness: 0.2 mm) obtained using the resin composition and a rubber sheet (raw sheet thickness: 2.5 mm) obtained using the rubber composition are bonded together and press vulcanized at 148° C. for 60 minutes, from which sheet-shaped test specimens having a width of 25 mm are produced. In the peeling test, the rubber layer of the sheet-shaped test specimens obtained is peeled at an angle of 180° from the resin layer at a peeling speed of 50 mm/minute at room temperature (23° C.) or at 70° C. using an autograph.
In the present technology, the adhesion strength between the rubber layer and the reinforcing layer (brass-plated wire) is the value obtained by measuring the adhesion strength (units=N/25 mm width) in a peeling test. The brass-plated wire is spiral-wound on a 25 mm external diameter steel mandrel, then the rubber sheet (raw sheet thickness: 2.5 mm) obtained using the rubber composition is bonded on top thereof, and vulcanization is carried out in a vulcanizer at 148° C. for 60 minutes, to obtain hose shaped test specimens. The rubber on the left and right of the hose-shaped test specimens obtained are cut so that the width of the rubber sheet is 25 mm, and a peeling test is carried out on the adhesion between the remaining rubber portion and wire portion by peeling the rubber from the reinforcing layer at room temperature (23° C.) using an autograph at a peeling speed of 50 mm/minute.
The rubber/resin composite hose of the present technology can be applied to, for example, a refrigerant transport hose (with carbon dioxide, HFC-134a (for car air conditioners), for example, as the refrigerant) or a hose for liquid propane gas (LPG hose).
The present technology is described below in detail using working examples but the present technology is not limited to such working examples.
The adhesion properties between the rubber and the resin (rubber/resin adhesion 1-4) and the adhesion properties between the reinforcing layer and the rubber layer were evaluated for the hose or laminates obtained as described below, using the following methods. The results thereof are shown in Tables 3, 4, 7, 8, 11, and 12 in
A phenolic resin adhesive (commercial name TY-PLY-BN (manufactured by LORD Far East, Inc.)) that was diluted by a factor of three in methyl ethyl ketone (MEK) was applied with a brush to a resin sheet 1 obtained as described below, and after drying, the resin sheet and a rubber sheet obtained as described below were bonded together, and press vulcanized at 148° C. for 60 minutes, to obtain sheet-shaped test specimens.
For Working Examples I-1, II-1, and III-1, the rubber/resin adhesion 1 results are shown for comparison/reference.
A resin sheet 1 obtained as described below and a rubber sheet obtained as described below were bonded together, and press vulcanized at 148° C. for 60 minutes, to obtain sheet-shaped test specimens. When they were bonded together, adhesive was not used.
A resin sheet 2 obtained as described below and a rubber sheet obtained as described below were bonded together, and press vulcanized at 148° C. for 60 minutes, to obtain sheet-shaped test specimens. When they were bonded together, adhesive was not used.
A resin sheet 3 (not including ionomer) obtained as described below and a rubber sheet obtained as described below were bonded together, and press vulcanized at 148° C. for 60 minutes, to obtain sheet-shaped test specimens. When they were bonded together, adhesive was not used.
For each of the sheet-shaped test specimens obtained, the adhesion strength (units=N/25 mm width) was measured by carrying out peeling tests. In the peeling test, the rubber layer was peeled at an angle of 180° from the resin layer at a peeling speed of 50 mm/minute at room temperature (23° C.) or at 70° C. using an autograph. Also, after the peeling tests, the rubber attachment (%, the area percentage of the rubber remaining without peeling from the resin layer) was determined visually, and the failure condition after the peeling test was observed.
The criteria for evaluation of the failure condition were, ⊚: material failure (thick material failure), ∘: material failure, Δ: material failure (thin material failure), x: interface, Cut: rubber cut.
First, a reinforcing layer was formed by spirally winding brass-plated wire on an iron mandrel having an outer diameter of 25 mm. Next, an unvulcanized sheet having a thickness of 2.5 mm that was prepared from each of the rubber compositions obtained was bonded onto the reinforcing layer, and vulcanized at 148° C. for 60 minutes, to manufacture hose-shaped test specimens.
For each of the hose-shaped test specimens obtained, the adhesion strength (units=N/25 mm width) and the rubber attachment (units=%, area percentage of rubber remaining without peeling) were measured when the rubber outer layer was peeled at a peeling speed of 50 mm/minute.
30 parts by mass of ionomer (ethylene-methacrylate resin copolymer with molecules crosslinked with zinc ions, trade name: Himilan 1706, manufactured by Dupont-Mitsui Polychemicals, Co., Ltd.) and 70 parts by mass of polyamide (11-Nylon, manufactured by Arkema) were mixed in a biaxial kneader, then it was extruded in a T die extruder to produce a sheet having a thickness of 0.2 mm. The resin sheet obtained was referred to as the resin sheet 1.
50 parts by mass of ionomer (ethylene-methacrylate resin copolymer with molecules crosslinked with zinc ions, trade name: Himilan 1706, manufactured by Dupont-Mitsui Polychemicals, Co., Ltd.) and 50 parts by mass of polyamide (11-Nylon, manufactured by Arkema) were mixed in a biaxial kneader, then it was extruded in a T die extruder to produce a sheet having a thickness of 0.2 mm. The resin sheet obtained was referred to as the resin sheet 2.
Polyamide (11-Nylon, manufactured by Arkema) was extruded in a T die extruder to produce a sheet having a thickness of 0.2 mm. The resin sheet obtained was referred to as the resin sheet 3.
Rubber sheets (unvulcanized) having a thickness of 2.5 mm were produced using a roll from rubber compositions A to C obtained as described below.
The rubber compositions were manufactured by uniformly mixing the components shown in Table 1 (
The components shown in Table 1 are as shown in Table 2 in
The components shown in Table 5 are as shown in Table 6 of
As can be seen from the results in Table 3, Table 4, Table 7, Table 8, Table 11, and Table 12 in
In contrast, in Working Examples I-1 to 18, Working Examples II-1 to 14, and Working Examples III-1 to 18, the adhesion between the resin layer and the rubber layer was excellent. Also, as can be seen from Working Example I-1 (results for rubber/resin adhesion 1 to 3), the adhesion between the resin layer and the rubber layer of the rubber/resin composite hose of the present technology (rubber/resin adhesion 2, 3) can be made equal to or greater than the adhesion between the resin layer and the rubber layer using current adhesives (rubber/resin adhesion 1). Likewise for Working Example II-1 and Working Example III-1.
In Working Examples II-3 to 14 and Working Examples III-3 to 18, the rubber composition further includes a thiuram vulcanization accelerator and/or a sulfenamide vulcanization accelerator, and an alkylphenol-formaldehyde resin, so adhesion to the brass-plated wire is enabled, while maintaining adhesion to the resin layer. Also, in the case of the sulfenamide accelerator, it was possible to provide adhesion between the resin layer and the rubber layer at high temperatures (for example, from 50 to 120° C.) that is equal to or greater than the case where the resin layer and the rubber layer are bonded using current adhesives (for example, TY-PLY-BN: a phenolic resin adhesive).
| Filing Document | Filing Date | Country | Kind | 371c Date |
|---|---|---|---|---|
| PCT/JP2011/078663 | 12/12/2011 | WO | 00 | 6/12/2014 |
