The present invention relates to a hose for transporting a refrigerant and a method of producing the same. More specifically, it relates to a hose for transporting a refrigerant that is used for a vehicle such as an automobile and a method of producing the same.
In recent days, according to the tighter control on production of ozone layer-depleting gas, more strict rules are imposed on a barrier property (i.e. refrigerant-permeability resistance) of a refrigerant transporting hose (i.e. a hose for an air-conditioner) used for an automobile or the like. For such reasons, a resin with high crystallinity such as polyamide resin is used as a material for a refrigerant transporting hose.
The polyamide resin has an excellent barrier property (i.e. refrigerant-permeability resistance). However, as having poor flexibility, there is a problem that it may be easily broken when a hose is bent. Thus, the polyamide resin alone is hardly used as a material for a refrigerant transporting hose. Instead, a polyamide resin mixed with a softer material than the resin, e.g. modified polyolefin, is used (see Patent Literature 1).
Compared to a case in which only the polyamide resin is used, the refrigerant transporting hose disclosed in Patent Literature 1 can have flexibility by mixing a modified polyolefin. However, there is still a problem that the breaking of the hose when it is bent (shaken) cannot be fully avoided.
The present invention is devised in view of the problems described above, and object of the invention is to provide a hose for transporting a refrigerant which can have both a barrier property (i.e. refrigerant-permeability resistance) and a flexibility and can solve the problem of hose breaking when the hose is bent, and a method of producing the hose for transporting a refrigerant.
To achieve the purpose of the invention described above, the first aspect of the invention is to provide a hose for transporting a refrigerant including a butyl rubber layer formed on an outer periphery of a tubular resin layer in contact with a refrigerant and an ethylene-propylene rubber layer formed on an outer periphery of the butyl layer, wherein the resin layer is composed of a material for resin layer which contains, as a main component, a mixture of a polyamide resin and a modified polyolefin elastomer and a skin layer is formed only on an inner peripheral surface of the resin layer so that tensile modulus (A) of the skin layer, tensile modulus (B) of the resin layer excluding the skin layer, tensile modulus (C) of the butyl rubber layer, and tensile modulus (D) of the ethylene-propylene rubber layer satisfy the relationship that is defined by the following formula (α):
(A)>(B)>(C)>(D) (α)
The second aspect of the invention relates to a method of producing the hose for transporting a refrigerant, i.e. a method of producing a hose for transporting a refrigerant including polishing an outer skin layer between an inner skin layer and an outer skin layer that are formed on an inner peripheral surface and an outer peripheral surface, respectively, of a tubular resin layer obtained by an extrusion of a material for resin layer containing, as a main component, a mixture of a polyamide resin and a modified polyolefin elastomer so as to remove the outer skin layer, forming a butyl rubber layer on the outer periphery of the resin layer, and further forming an ethylene-propylene rubber layer on the outer periphery of the butyl rubber layer.
Specifically, inventors carried out intensive studies to obtain a refrigerant transporting hose having both a barrier property (i.e. refrigerant-permeability resistance) and flexibility which enables solving the problem of breaking hose at the time of bending. It was found during the course of the studies that, when a material for a resin layer containing, as a main component, a mixture of a polyamide resin and a modified polyolefin elastomer, is extruded to have a hose shape, an inner skin layer 2 and an outer skin layer 3, both have thickness of about 3 to 5 μm and are made of a polyamide resin 4, are formed on an inner peripheral surface and an outer peripheral surface, respectively, of a tubular resin layer 1 (see
As described above, an outer skin layer which cannot adapt to hose deformation when the hose is bent is removed from a resin layer surface of the refrigerant transporting hose of the invention. Further, it has a constitution in which an inner skin layer that is the innermost layer, an outer resin layer, a butyl rubber layer, and an ethylene-propylene rubber layer are provided in the order so that tensile modulus (hardness) of each layer sequentially decreases. As such, according to the invention, stress concentration can be relieved when a hose is bent and adaptation to hose deformation can be obtained, and therefore the breaking hose problem can be avoided. Further, because the tubular resin layer is composed of a material for a resin layer which contains, as a main component, a mixture of polyamide resin having an excellent barrier property (i.e. refrigerant-permeability resistance) and a modified polyolefin elastomer having flexibility, it can have both the barrier property (i.e. refrigerant-permeability resistance) and flexibility.
Further, when modification in the modified polyolefin elastomer is at least anyone of maleic anhydride modification and epoxy modification, flexibility of the hose can be improved.
Further, by having the mixing ratio between the polyamide resin (a) and the modified polyolefin elastomer (b) within the range of (a)/(b)=90/10 to 60/40 in terms of weight, a favorable balance between the barrier property (i.e. refrigerant-permeability resistance) and the flexibility can be obtained as caused by the polyamide resin having excellent barrier property (i.e. refrigerant-permeability resistance) and the modified polyolefin elastomer having flexibility.
Still further, when the refrigerant transporting hose of the present invention is produced by polishing an outer skin layer to remove the outer skin layer, forming a butyl rubber layer on the outer periphery thereof, and forming an ethylene-propylene rubber layer on the outer periphery of the butyl rubber layer, unevenness on the outer peripheral surface (removal surface) 1a of the resin layer 1 is yielded by the polishing as illustrated in
Herein below, embodiments of the invention are explained in detail. However, it is evident that the invention is not limited by them.
The refrigerant transporting hose of the invention is composed of, as illustrated in
According to an embodiment of the invention, a skin layer 6 that is the innermost layer, an outer resin layer 1, a butyl rubber layer 7, and an ethylene-propylene rubber 8 are provided in this order so that tensile modulus (hardness) of each layer sequentially decreases. Specifically, tensile modulus (A) of the skin layer 6, tensile modulus (B) of the resin layer 1 excluding the skin layer 6, tensile modulus (C) of the butyl rubber layer 7, and tensile modulus (D) of the ethylene-propylene rubber layer 8 satisfy the relationship that is defined by the following formula (α), and it is the most unique feature of the invention:
(A)>(B)>(C)>(D) (α)
The tensile modulus (A) of the skin layer 6 is preferably in the range of 3000 to 2000 MPa. Particularly preferably, it is in the range of 2600 to 2400 MPa. The tensile modulus (B) of the resin layer 1 is preferably in the range of less than 2000 MPa and 500 MPa or higher. Particularly preferably, it is in the range of 1000 to 600 MPa. The tensile modulus (C) of the butyl rubber layer 7 is preferably in the range of less than 500 MPa and 10 MPa or higher. Particularly preferably, it is in the range of 20 to 10 MPa. The tensile modulus (D) of the ethylene-propylene rubber layer 8 is preferably less than 10 MPa. Particularly preferably, it is less than 7 MPa.
Tensile modulus (hardness) of each layer indicates the value measured according to JIS K 7127 under the elongation rate condition of 5±1.0 mm per minute. Tensile modulus (hardness) of each layer can be measured by using, for example, a universal hardness tester, a micro hardness tester, or the like.
Herein below, materials for forming each layer of the refrigerant transporting hose of the invention are explained.
The resin layer 1 of the refrigerant transporting hose of the invention is formed by using a material for a resin layer which contains, as a main component, a mixture of a polyamide resin and a modified polyolefin elastomer.
Examples of the polyamide resin include polyamide 6 (PA6), polyamide 11 (PA11), polyamide 12 (PA12), polyamide 46 (PA46), polyamide 66 (PA66), polyamide 92 (PA92), polyamide 99 (PA99), polyamide 610 (PA610), polyamide 612 (PA612), polyamide 912 (PA912), polyamide 1010 (PA1010), a copolymer of polyamide 6 and polyamide 12 (PA6/12), a copolymer of polyamide 6 and polyamide 66 (PA6/66), aromatic nylon, and the like. It may be used either singly or in combination of two or more. Of these, as having an excellent barrier property (i.e. refrigerant-permeability resistance) and excellent interlayer adhesion, polyamide 6 is preferable.
Modified polyolefin elastomer is obtained by chemical modification of a polymer side chain or terminal of a polyolefin elastomer with maleic anhydride, silicone (silane), chlorine, amine, acryl, an epoxy compound, or the like, wherein the polyolefin elastomer is prepared by homopolymerization or copolymerization of an olefin such as ethylene, propylene, and butadiene, or a diene monomer. The modified polyolefin elastomer is used either singly or in combination of two or more. Of these, from the viewpoint of excellent adhesion and processability, an ethylene-propylene-diene ternary copolymer rubber (EPDM) modified with maleic anhydride or a copolymer of glycidyl methacrylate and ethylene (epoxy modified polyolefin elastomer) are preferable.
The mixing ratio between the polyamide resin (a) and the modified polyolefin elastomer (b) is preferably (a)/(b)=90/10 to 60/40, in terms of weight ratio. Particularly preferably, it is in the range of (a)/(b)=85/15 to 70/30. In other words, when the mixing ratio of the polyamide resin (a) is too high, flexibility tends to get deteriorated. On the other hand, when the mixing ratio of the polyamide resin (a) is too low, the barrier property (i.e. refrigerant-permeability resistance) tends to get deteriorated.
Examples of the mixture of the polyamide resin and the modified polyolefin elastomer include an alloy of the polyamide resin and the modified polyolefin elastomer, and the like.
Further, the material for forming the resin layer 1 (i.e. resin material) may be suitably added with, in addition to the mixture of the polyamide resin and the modified polyolefin elastomer, additives such as a filler, a plasticizer, and an anti-aging agent, if necessary. The additives may be used either singly or in combination of two or more.
As illustrated in
Further, as explained above, although the outer skin layer 3 is also formed on an outer peripheral surface of the tubular resin layer 1 by an extrusion process of the materials for resin layer (see
As illustrated in
Examples of the butyl rubber that can be used include butyl rubber (IIR), halogenated butyl rubber, or the like. It may be used either singly or in combination of two or more. Examples of the halogenated butyl rubber include chlorinated butyl rubber (Cl-IIR), brominated butyl rubber (Br-IIR), and the like.
Examples of the resin cross-linking agent include formaldehyde condensate of alkyl phenol, and the like. More specific examples of the resin cross-linking agent include alkyl phenol.formaldehyde condensate (trade name: TACKIROL 201MB35, manufactured by Taoka Chemical Co., Ltd.), and the like.
Content of the resin cross-linking agent is preferably 20 to 40 parts by weight relative to 100 parts by weight of the butyl rubber.
Examples of the process aid include stearic acid, and the like.
Content of the process aid is preferably 0.5 to 2 parts by weight relative to 100 parts by weight of the butyl rubber.
Examples of the carbon black include SAF, ISAF, HAF, MAF, FEF, GPF, SRF, FT, MT grade carbon black, and the like. It may be used either singly or in combination or two or more. Of these, ISAF grade carbon black is preferable.
Content of the carbon black is preferably 10 to 40 parts by weight relative to 100 parts by weight of the butyl rubber.
Examples of the filler include an inorganic compound originating from minerals such as talc and mica. It may be used either singly or in combination of two or more.
Content of the filler is preferably 1 to 20 parts by weight relative to 100 parts by weight of the butyl rubber.
Examples of the softening agent include a petroleum-based softening agent such as process oil, lubricant, paraffin, fluid paraffin, petroleum asphalt, and vaseline, an oil-based softening agent such as castor oil, rape seed oil, canola oil, and palm oil, waxes such as tall oil, sap, bee wax, carnauba wax, and lanolin, linolenic acid, palmitic acid, stearic acid, lauric acid, and the like. It may be used either singly or in combination of two or more.
Content of the softening agent is preferably 0.5 to 10 parts by weight relative to 100 parts by weight of the butyl rubber.
Content of the zinc oxide is preferably 1 to 10 parts by weight relative to 100 parts by weight of the butyl rubber.
Examples of the adhesive component include a resorcinol compound, a melamine compound, and the like. It may be used either singly or in combination of two or more.
It is preferable that the resorcinol compound is mainly used as adhesives. Examples thereof include modified resorcin.formaldehyde resin, resorcin, resorcin.formaldehyde (RF) resin, and the like. It may be used either singly or in combination of two or more. Of these, from the viewpoint of transpiration and compatibility with rubber, modified resorcin.formaldehyde resin is preferably used.
Examples of the modified resorcin.formaldehyde resin include those represented by the following formula (1) to formula (3). It may be used either singly or in combination of two or more. Of these, those represented by the formula (I) are particularly preferable.
Examples of the melamine compound include methylated product of formaldehyde.melamine polymer, hexamethylene tetramine, and the like. It may be used either singly or in combination of two or more. It is decomposed by heat during cross-linking to provide the system with formaldehyde. Among them, from the viewpoint of low volatility and good compatibility with rubber, methylated product of formaldehyde.melamine polymer is preferable.
Preferred examples of the methylated product of formaldehyde.melamine polymer include those represented by the following formula (4). In particular, among those represented by the formula (4), a mixture containing 43 to 44% by weight of the compound wherein n=1, 27 to 30% by weight of the compound wherein n=2, and 26 to 30% by weight of the compound wherein n=3 is preferable.
Content of the adhesive component (resorcin compound and melamine compound and the like) is preferably 5 parts by weight or less relative to 100 parts by weight of the butyl rubber.
The butyl rubber composition can be prepared by mixing each components and kneading them by using a blending machine such as a kneader, a banbury mixer, or a roll.
As illustrated in
Examples of the ethylene-propylene rubber include an ethylene-propylene-diene ternary copolymer rubber (EPDM), ethylene-propylene copolymer rubber (EPM), and the like. It may be used either singly or in combination of two or more.
As for the ethylene-propylene rubber, those having iodine value within the range of 16 to 28 and ethylene ratio within the range of 48 to 70% by weight are preferable, from the viewpoint of excellent stability under high temperature and high pressure condition. Those having iodine value within the range of 6 to 26 and ethylene ratio within the range of 48 to 75% by weight are particularly preferable.
As a diene monomer included in the EPDM (i.e. a third component), a diene monomer having 5 to 20 carbon atoms is preferable. Specific examples of the preferred monomer include 1,4-pentadiene, 1,4-hexadine, 1,5-hexadiene, 2,5-dimethyl-1,5-hexadiene, 1,4-octadiene, 1,4-cyclohexadiene, cyclooctadiene, dicyclopentadiene (DCP), 5-ethylidene-2-norbornene (ENS), 5-butylidene-2-norbornene, 2-methyl-5-norbornene, 2-isopropenyl-5-norbornene, and the like. Among these diene monomers (i.e. a third component), dicyclopentadiene (DCP) and 5-ethylidene-2-norbornene (ENS) are preferable.
Examples of the process aid include stearic acid, and the like.
Content of the process aid is preferably 0.5 to 2 parts by weight relative to 100 parts by weight of the ethylene-propylene rubber.
Content of the zinc oxide is preferably 1 to 10 parts by weight relative to 100 parts by weight of the ethylene-propylene rubber.
Content of the tackifier is preferably 0.5 to 4 parts by weight relative to 100 parts by weight of the ethylene-propylene rubber.
As for the carbon black, those having excellent extrusion processability or reinforcing property are preferable. Examples of the carbon black include various kinds of SAF, ISAF, HAF, MAF, FEF, GPF, SRF, FT, MT grade carbon black, and the like. It may be used either singly or in combination or two or more. Of these, FEF grade carbon black is preferable.
Content of the carbon black is preferably 50 to 150 parts by weight relative to 100 parts by weight of the ethylene-propylene rubber.
Examples of the vulcanizing aid include zinc oxide (ZnO), magnesium oxide, and the like. It may be used either singly or in combination or two or more.
Content of the vulcanizing aid is preferably 0.5 to 2 parts by weight relative to 100 parts by weight of the ethylene-propylene rubber.
Examples of the softening agent include a petroleum-based softening agent such as process oil, lubricant, paraffin, fluid paraffin, petroleum asphalt, and vaseline, an oil-based softening agent such as castor oil, rape seed oil, canola oil, and palm oil, waxes such as tall oil, sap, bee wax, carnauba wax, and lanolin, linolenic acid, palmitic acid, stearic acid, lauric acid, and the like. It may be used either singly or in combination of two or more.
Content of the softening agent is preferably 50 to 90 parts by weight relative to 100 parts by weight of the ethylene-propylene rubber.
Examples of the vulcanizing promoter include a vulcanizing promoter such as thioram, dithiocarbamic acid salt, and sulfen amide. It may be used either singly or in combination of two or more.
Content of the vulcanizing promoter is preferably 0.2 to 2 parts by weight relative to 100 parts by weight of the ethylene-propylene rubber.
Examples of the thioram vulcanizing promoter include tetramethyl thioram disulfide (TT), tetraethyl thioram disulfide (TET), tetrabutyl thioram disulfide (TBTD), tetrakis(2-ethylhexyl)thioram disulfide (TOT), tetrabenzyl thioram disulfide (TBZTD), and the like. It may be used either singly or in combination of two or more.
Examples of the sulfen amide vulcanizing promoter include N-oxydiethylene-2-benzothiazolyl sulfen amide (NOBS), N-cyclohexyl-2-benzothiazolyl sulfen amide (CM), N-t-butyl-2-benzothiazolyl sulfen amide (BBS), N,N′-dicyclohexyl-2-benzothiazolyl sulfen amide, and the like. It may be used either singly or in combination of two or more.
Examples of the vulcanizing agent include sulfur, peroxide vulcanizing agent (peroxide sulfurizing agent), and the like, and it may be used either singly or in combination of two or more. Of these, from the view point of storage stability and cost, sulfur is preferable.
Content of the vulcanizing agent is preferably 0.5 to 2 parts by weight relative to 100 parts by weight of the ethylene-propylene rubber.
The ethylene-propylene rubber composition can be prepared by mixing each components and kneading them by using a blending machine such as a kneader, a banbury mixer, or a roll.
At an interface between the butyl rubber layer 7 and the ethylene-propylene rubber layer 8, a reinforcing layer 9 is provided. Examples of the material for forming the reinforcing layer 9 include reinforcing wire materials such as polyethylene terephthalate (PET), polyethylene naphthalate (PEN), aramide, polyamide, vinylon, rayon, and metal wire. The reinforcing layer 9 can be produced by braiding the reinforcing wire materials by spiral braiding, blade braiding, knit braiding, or the like.
Next, a method of producing a refrigerant transporting hose is explained. First, by extruding a material for resin layer containing a mixture of a polyamide resin and a modified polyolefin elastomer as a main component on a mandrel (not illustrated) to form in a hose shape, a tubular resin layer 1 is formed (see
Next, on an outer peripheral surface (removal layer) 1a of the resin layer 1 from which the outer skin layer 3 is removed, butyl rubber material (i.e. butyl rubber composition) is extruded to form a butyl rubber layer 7 as illustrated in
The polishing treatment can be carried out by using a polishing brush such as wire brush or a polishing file. According to the invention, the polishing treatment can be carried out by, for example, rotating a spiral polishing brush or a polishing file at pre-determined rotation number and rotation rate and supplying continuously the tubular resin layer 1 (see
Examples of the material of a polishing brush such as wire brush or a polishing file include stainless steel, carbon, and the like.
With respect to the refrigerant transporting hose of the invention, inner diameter of the hose is preferably in the range of 5 to 40 mm. Further, thickness of the resin layer 1 is preferably in the range of 0.01 to 0.5 mm, and particularly preferably in the range of 0.10 to 0.20 mm. Thickness of the skin layer 6 is preferably in the range of 1 to 7 μm, and particularly preferably in the range of 3 to 5 μm. Thickness of the butyl rubber layer 7 is generally in the range of 1 to 2 mm, and the thickness of the ethylene-propylene rubber layer 8 is generally in the range of 0.5 to 2 mm.
Herein below, the Examples are explained along with the Comparative examples. However, it is evident that the invention is not limited by these Examples.
By using a double-axis kneader (manufactured by JSW STEEL LTD.), polyamide 6 (PA6) (trade name: NYLON 6 1030B, manufactured by Ube Industries, Ltd.) as a polyamide resin and maleic anhydride modified EPDM (trade name: TAFMER MH7020, manufactured by Mitsui Chemicals, Inc.) as a modified polyolefin elastomer were mixed at the temperature the same or higher than the melting point of the polyamide resin (250° C.). The mixing ratio (weight ratio) between the polyamide resin (a) and the modified polyolefin elastomer (b) was (a)/(b)=70/30.
100 parts by weight of chlorinated butyl rubber (CI-IIR) (trade name: BUTYL HT1066, manufactured by JSR CORPORATION), 1 part by weight of stearic acid (trade name: LUNAC S30, manufactured by Kao Corporation), 20 parts by weight of FEF grade carbon black (trade name: SEAST SO, manufactured by TOKAI CARBON CO., LTD.), 100 parts by weight of talc (trade name: MICRO ACE K-1, manufactured by NIPPON TALC Co., Ltd.), 10 parts by weight of naphthene oil (trade name: DIANA PROCESS NM-300, manufactured by Idemitsu Kosan Co., Ltd.) as a softening agent, and 30 parts by weight of resin vulcanizing agent (trade name: TACKIROL 201-35M/B, manufactured by Taoka Chemical Co., Ltd.) were admixed with one another and kneaded by using a banbury mixer (manufactured by Kobe Steel, Ltd.) and a roll (manufactured by Nippon Roll MFG. Co., Ltd.) to prepare a butyl rubber composition.
100 parts by weight of EPDM (trade name: ESPRENE 532T, manufactured by Sumitomo Chemical Co., Ltd.), 1 part by weight of stearic acid (trade name: LUNAC S30, manufactured by Kao Corporation), 5 parts by weight of zinc oxide (two kinds of zinc oxide, manufactured by MITSUI MINING & SMELTING CO., LTD.), 100 parts by weight of FEF grade carbon black (trade name: SEAST SO, manufactured by TOKAI CARBON CO., LTD.), 70 parts by weight of naphthene oil (trade name: DIANA PROCESS NM-300, manufactured by Idemitsu Kosan Co., Ltd.) as a softening agent, 1 part by weight of thioram vulcanizing promoter (trade name: SANCELER TT-G, manufactured by SANSHIN CHEMICAL INDUSTRY CO., LTD.), 1 part by weight of dithiocarbamic acid salt vulcanizing promoter (trade name: SANCELER BZ-G, manufactured by SANSHIN CHEMICAL INDUSTRY CO., LTD.), and 1 part by weight of vulcanizing agent (sulfur) (trade name: SULFUR PTC, manufactured by DAITO SANGYO CO., LTD.) were admixed with one another and kneaded by using a banbury mixer (manufactured by Kobe Steel, Ltd.) and a roll (manufactured by Nippon Roll MFG. Co., Ltd.) to prepare an ethylene-propylene rubber composition.
By using a TPX mandrel (outer diameter: 12 mm, manufactured by Mitsui Chemical, Inc.), the material for resin layer was extruded on the mandrel to form in a hose shape, and thus a tubular resin layer (thickness: 0.15 mm) having an inner skin layer (thickness: 4 μm) and an outer skin layer (thickness: 4 μm) was formed. Next, the outer peripheral surface was subjected to a polishing treatment using a wire brush (manufactured by State industry Co., Ltd.) to completely remove the outer skin layer. Subsequently, the butyl rubber composition which has been prepared above was extruded on the outer peripheral surface of the resin layer to form a butyl rubber layer thereon. Then, on the outer peripheral surface thereof a reinforcing layer was formed by blade braiding with polyester threads. Further, the ethylene-propylene rubber composition which has been prepared above was extruded on the outer peripheral surface of the reinforcing layer to form an ethylene-propylene rubber layer thereon. After vulcanization (170° C.×30 min), the mandrel was removed and the resulting long laminated hose was cut to have desired length. As a result, a hose constituted of the skin layer (thickness: 4 μm), the resin layer (thickness: 0.15 mm), the butyl rubber layer (thickness: 2.0 mm), the reinforcing layer, and EPDM layer (thickness: 1.0 mm) in the order was obtained.
By using a double-axis kneader (manufactured by JSW STEEL LTD.), polyamide 66 (PA66) (trade name: NYLON 66 2015B, manufactured by Ube Industries, Ltd.) as a polyamide resin and maleic anhydride modified EPDM (trade name: TAFMER MH7020, manufactured by Mitsui Chemicals, Inc.) as a modified polyolefin elastomer were mixed at the temperature the same or higher than the melting point of the polyamide resin (270° C.). The mixing ratio (weight ratio) between the polyamide resin (a) and the modified polyolefin elastomer (b) was (a)/(b)=70/30.
A hose was produced in the same manner as in Example 1 except using the resin layer material prepared above.
By using a double-axis kneader (manufactured by JSW STEEL LTD.), polyamide 6 (PA6) (trade name: NYLON 6 1030B, manufactured by Ube Industries, Ltd.) as a polyamide resin and a copolymer of glycidyl methacrylate and ethylene (trade name: BONDFAST 2C, manufactured Sumitomo Chemical Co., Ltd.) were mixed at the temperature the same or higher than the melting point of the polyamide resin (250° C.). The mixing ratio (weight ratio) between the polyamide resin (a) and the modified polyolefin elastomer (b) was (a)/(b)=80/20.
A hose was produced in the same manner as in Example 1 except using the resin layer material prepared above.
By using a double-axis kneader (manufactured by JSW STEEL LTD.), polyamide 6T (PA6T) (trade name: NYLON 6T RENY 6002, manufactured by Mitsubishi Engineering-Plastics Corporation) as an aromatic polyamide resin and maleic anhydride modified EPDM (trade name: TAFMER MH7020, manufactured by Mitsui Chemicals, Inc.) as a modified polyolefin elastomer were mixed at the temperature the same or higher than the melting point of the polyamide resin (250° C.). The mixing ratio (weight ratio) between the polyamide resin (a) and the modified polyolefin elastomer (b) was (a)/(b)=90/10.
A hose was produced in the same manner as in Example 1 except using the resin layer material prepared above.
The resin layer material was prepared in the same manner as in Example 1 except that polyamide 92 (PA92) (trade name: 400B, manufactured by Ube Industries, Ltd.), which is as a polycondensate of nonane diamine and dibutyl oxalate (i.e. polyoxiamide resin), is used instead of polyamide 6 (PA6) (trade name: NYLON 6 1030B, manufactured by Ube Industries, Ltd.) as a polyamide resin.
Then, a hose was produced in the same manner as in Example 1 except using the resin layer material prepared above.
A hose was produced in the same manner as in Example 1 except that no polishing treatment is performed to remove the outer skin layer. Specifically, with reference to the Example 1, a hose in which the inner skin layer (thickness: 4 μm), the resin layer (thickness: 0.15 mm), the outer skin layer (thickness: 4 μm), the butyl rubber layer (thickness: 2.0 mm), the reinforcing layer, and EPDM layer (thickness: 1.0 mm) are formed in the order was obtained.
Characteristics of the hoses obtained from the Examples and the Comparative Examples were evaluated according to the criteria described below. The evaluation results are summarized in the following Table 1.
[Tensile Modulus of Each Layer]
Tensile modulus (hardness) was measured for each layer by using a universal hardness tester (manufactured by MEISHIN KOKI Co., Ltd.). Further, the tensile modulus (hardness) of each layer represents the value measured with reference to JIS K 7127 under the elongation rate of 5±1.0 mm per minute.
[Interlayer Adhesion]
A sample for adhesion evaluation was cut out from each hose (width: 20 mm, length 100 mm). The butyl rubber layer side of the sample was fixed on a tensile tester (JIS B 7721) and the sample was elongated at the resin layer side with elongation rate of 50 mm per minute. Then, the peeling between the rubber layer and the resin layer was examined with a naked eye. When the rubber layer is fractured, it was labeled as “fracture of rubber.”
[Bending Fatigue]
To evaluate the bending fatigue of each hose, the whip test was performed as follows. Specifically, as illustrated in
As shown in the results of Table 1 above, the tensile modulus (hardness) of each layer gradually decreases in the product of the Examples because the outer skin layer is removed by a polishing treatment. Accordingly, even after the bending fatigue test, the product of the Examples did not show any fracture in the resin layer.
On the other hand, the tensile modulus (hardness) of each layer does not gradually decrease in the product of the Comparative Example 1 because the outer skin layer which whose tensile modulus (hardness) is higher than that of the resin layer is present on an outer peripheral surface of the resin layer. As such, in the Comparative Example 1, local stress concentration occurs at the outer skin layer, and as a result, a fracture in the resin layer is shown in the bending fatigue test.
Meanwhile, although in Examples described above specific embodiments of the invention are shown, the Examples are for the purposes of exemplification only, and they are not to be construed to limit the invention. Further, any modifications belonging to the equivalents of the Claims are also within the scope of the invention.
The refrigerant transporting hose of the invention is used as a hose for transporting a refrigerant such as carbon dioxide, freon, freon substitute, and propane that are used for an air conditioner radiator, or the like. Further, the refrigerant transporting hose of the invention may be also used not only for automobiles but also for other transporting vehicles (e.g. an industrial transporting vehicle such as an airplane, a fork lift, a shovel car, and a crane, a railway vehicle, and the like), or the like.
Number | Date | Country | Kind |
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2010-218673 | Sep 2010 | JP | national |
2011-056921 | Mar 2011 | JP | national |
Number | Date | Country | |
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Parent | PCT/JP2011/068652 | Aug 2011 | US |
Child | 13408274 | US |