WO2005097903A1 - ポリアミド系複合樹脂及び冷媒輸送用ホース - Google Patents
ポリアミド系複合樹脂及び冷媒輸送用ホース Download PDFInfo
- Publication number
- WO2005097903A1 WO2005097903A1 PCT/JP2005/005096 JP2005005096W WO2005097903A1 WO 2005097903 A1 WO2005097903 A1 WO 2005097903A1 JP 2005005096 W JP2005005096 W JP 2005005096W WO 2005097903 A1 WO2005097903 A1 WO 2005097903A1
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- WIPO (PCT)
- Prior art keywords
- polyamide
- resin
- layer
- polyolefin
- refrigerant transport
- Prior art date
Links
- 229920002647 polyamide Polymers 0.000 title claims abstract description 110
- 239000003507 refrigerant Substances 0.000 title claims abstract description 81
- 239000004952 Polyamide Substances 0.000 title claims abstract description 79
- 239000000805 composite resin Substances 0.000 title claims abstract description 48
- 229920000098 polyolefin Polymers 0.000 claims abstract description 87
- 239000011347 resin Substances 0.000 claims description 112
- 229920005989 resin Polymers 0.000 claims description 112
- 229920002292 Nylon 6 Polymers 0.000 claims description 35
- 239000000203 mixture Substances 0.000 claims description 14
- 238000000034 method Methods 0.000 claims description 10
- -1 metaxylene diamine Chemical class 0.000 claims description 6
- IVSZLXZYQVIEFR-UHFFFAOYSA-N 1,3-Dimethylbenzene Natural products CC1=CC=CC(C)=C1 IVSZLXZYQVIEFR-UHFFFAOYSA-N 0.000 claims description 5
- 239000000470 constituent Substances 0.000 claims description 3
- FDLQZKYLHJJBHD-UHFFFAOYSA-N [3-(aminomethyl)phenyl]methanamine Chemical compound NCC1=CC=CC(CN)=C1 FDLQZKYLHJJBHD-UHFFFAOYSA-N 0.000 claims 1
- 230000004888 barrier function Effects 0.000 abstract description 37
- 239000000956 alloy Substances 0.000 abstract description 9
- 229910045601 alloy Inorganic materials 0.000 abstract description 9
- 239000003795 chemical substances by application Substances 0.000 abstract description 8
- 229920000642 polymer Polymers 0.000 abstract description 7
- 239000010410 layer Substances 0.000 description 143
- 229920001971 elastomer Polymers 0.000 description 52
- 239000005060 rubber Substances 0.000 description 52
- 229920001577 copolymer Polymers 0.000 description 12
- 230000003014 reinforcing effect Effects 0.000 description 11
- 239000000126 substance Substances 0.000 description 11
- 238000002156 mixing Methods 0.000 description 10
- 238000001125 extrusion Methods 0.000 description 9
- 230000000052 comparative effect Effects 0.000 description 6
- 230000000694 effects Effects 0.000 description 6
- 229920000728 polyester Polymers 0.000 description 6
- 238000012360 testing method Methods 0.000 description 6
- 238000009472 formulation Methods 0.000 description 5
- 238000004898 kneading Methods 0.000 description 5
- 239000002245 particle Substances 0.000 description 5
- 229920002943 EPDM rubber Polymers 0.000 description 4
- 239000004594 Masterbatch (MB) Substances 0.000 description 4
- 229920005549 butyl rubber Polymers 0.000 description 4
- 238000011156 evaluation Methods 0.000 description 4
- 229920003049 isoprene rubber Polymers 0.000 description 4
- 239000000463 material Substances 0.000 description 4
- 229920000459 Nitrile rubber Polymers 0.000 description 3
- 239000004677 Nylon Substances 0.000 description 3
- 239000003963 antioxidant agent Substances 0.000 description 3
- 229920001778 nylon Polymers 0.000 description 3
- 239000002356 single layer Substances 0.000 description 3
- 229920001897 terpolymer Polymers 0.000 description 3
- 239000004711 α-olefin Substances 0.000 description 3
- 239000000654 additive Substances 0.000 description 2
- 239000012790 adhesive layer Substances 0.000 description 2
- 230000032683 aging Effects 0.000 description 2
- 230000003078 antioxidant effect Effects 0.000 description 2
- 230000005540 biological transmission Effects 0.000 description 2
- 229920005556 chlorobutyl Polymers 0.000 description 2
- 229920006244 ethylene-ethyl acrylate Polymers 0.000 description 2
- 229920001519 homopolymer Polymers 0.000 description 2
- 229920000554 ionomer Polymers 0.000 description 2
- 238000004519 manufacturing process Methods 0.000 description 2
- 238000001000 micrograph Methods 0.000 description 2
- 238000000465 moulding Methods 0.000 description 2
- 229920001084 poly(chloroprene) Polymers 0.000 description 2
- 238000003878 thermal aging Methods 0.000 description 2
- QLZJUIZVJLSNDD-UHFFFAOYSA-N 2-(2-methylidenebutanoyloxy)ethyl 2-methylidenebutanoate Chemical class CCC(=C)C(=O)OCCOC(=O)C(=C)CC QLZJUIZVJLSNDD-UHFFFAOYSA-N 0.000 description 1
- 241000531908 Aramides Species 0.000 description 1
- 241001474374 Blennius Species 0.000 description 1
- ZAMOUSCENKQFHK-UHFFFAOYSA-N Chlorine atom Chemical compound [Cl] ZAMOUSCENKQFHK-UHFFFAOYSA-N 0.000 description 1
- 229920000089 Cyclic olefin copolymer Polymers 0.000 description 1
- 239000004593 Epoxy Substances 0.000 description 1
- 239000006057 Non-nutritive feed additive Substances 0.000 description 1
- 239000004698 Polyethylene Substances 0.000 description 1
- 229920000297 Rayon Polymers 0.000 description 1
- 229920002978 Vinylon Polymers 0.000 description 1
- 150000008065 acid anhydrides Chemical class 0.000 description 1
- 229920000800 acrylic rubber Polymers 0.000 description 1
- 125000005250 alkyl acrylate group Chemical group 0.000 description 1
- 229920003235 aromatic polyamide Polymers 0.000 description 1
- 125000003118 aryl group Chemical group 0.000 description 1
- 229920005557 bromobutyl Polymers 0.000 description 1
- 229910052801 chlorine Inorganic materials 0.000 description 1
- 239000000460 chlorine Substances 0.000 description 1
- 238000013329 compounding Methods 0.000 description 1
- 238000007796 conventional method Methods 0.000 description 1
- 230000006866 deterioration Effects 0.000 description 1
- 239000006185 dispersion Substances 0.000 description 1
- 229920006226 ethylene-acrylic acid Polymers 0.000 description 1
- 239000000945 filler Substances 0.000 description 1
- VOZRXNHHFUQHIL-UHFFFAOYSA-N glycidyl methacrylate Chemical compound CC(=C)C(=O)OCC1CO1 VOZRXNHHFUQHIL-UHFFFAOYSA-N 0.000 description 1
- 229920002681 hypalon Polymers 0.000 description 1
- 230000001771 impaired effect Effects 0.000 description 1
- 230000006872 improvement Effects 0.000 description 1
- 238000010030 laminating Methods 0.000 description 1
- 239000007788 liquid Substances 0.000 description 1
- 230000007774 longterm Effects 0.000 description 1
- FPYJFEHAWHCUMM-UHFFFAOYSA-N maleic anhydride Chemical compound O=C1OC(=O)C=C1 FPYJFEHAWHCUMM-UHFFFAOYSA-N 0.000 description 1
- 239000000178 monomer Substances 0.000 description 1
- 230000001590 oxidative effect Effects 0.000 description 1
- 230000035699 permeability Effects 0.000 description 1
- 229920003207 poly(ethylene-2,6-naphthalate) Polymers 0.000 description 1
- 229920000058 polyacrylate Polymers 0.000 description 1
- 229920006122 polyamide resin Polymers 0.000 description 1
- 229920001230 polyarylate Polymers 0.000 description 1
- 229920000573 polyethylene Polymers 0.000 description 1
- 239000011112 polyethylene naphthalate Substances 0.000 description 1
- 239000002994 raw material Substances 0.000 description 1
- 239000002964 rayon Substances 0.000 description 1
- 230000009467 reduction Effects 0.000 description 1
- 239000011342 resin composition Substances 0.000 description 1
- 238000010074 rubber mixing Methods 0.000 description 1
- 230000008719 thickening Effects 0.000 description 1
- 238000004073 vulcanization Methods 0.000 description 1
- 230000004580 weight loss Effects 0.000 description 1
Classifications
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B32—LAYERED PRODUCTS
- B32B—LAYERED PRODUCTS, i.e. PRODUCTS BUILT-UP OF STRATA OF FLAT OR NON-FLAT, e.g. CELLULAR OR HONEYCOMB, FORM
- B32B1/00—Layered products having a non-planar shape
- B32B1/08—Tubular products
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B32—LAYERED PRODUCTS
- B32B—LAYERED PRODUCTS, i.e. PRODUCTS BUILT-UP OF STRATA OF FLAT OR NON-FLAT, e.g. CELLULAR OR HONEYCOMB, FORM
- B32B27/00—Layered products comprising a layer of synthetic resin
- B32B27/34—Layered products comprising a layer of synthetic resin comprising polyamides
-
- F—MECHANICAL ENGINEERING; LIGHTING; HEATING; WEAPONS; BLASTING
- F16—ENGINEERING ELEMENTS AND UNITS; GENERAL MEASURES FOR PRODUCING AND MAINTAINING EFFECTIVE FUNCTIONING OF MACHINES OR INSTALLATIONS; THERMAL INSULATION IN GENERAL
- F16L—PIPES; JOINTS OR FITTINGS FOR PIPES; SUPPORTS FOR PIPES, CABLES OR PROTECTIVE TUBING; MEANS FOR THERMAL INSULATION IN GENERAL
- F16L11/00—Hoses, i.e. flexible pipes
- F16L11/04—Hoses, i.e. flexible pipes made of rubber or flexible plastics
- F16L11/045—Hoses, i.e. flexible pipes made of rubber or flexible plastics with four or more layers without reinforcement
-
- F—MECHANICAL ENGINEERING; LIGHTING; HEATING; WEAPONS; BLASTING
- F16—ENGINEERING ELEMENTS AND UNITS; GENERAL MEASURES FOR PRODUCING AND MAINTAINING EFFECTIVE FUNCTIONING OF MACHINES OR INSTALLATIONS; THERMAL INSULATION IN GENERAL
- F16L—PIPES; JOINTS OR FITTINGS FOR PIPES; SUPPORTS FOR PIPES, CABLES OR PROTECTIVE TUBING; MEANS FOR THERMAL INSULATION IN GENERAL
- F16L11/00—Hoses, i.e. flexible pipes
- F16L11/04—Hoses, i.e. flexible pipes made of rubber or flexible plastics
- F16L2011/047—Hoses, i.e. flexible pipes made of rubber or flexible plastics with a diffusion barrier layer
Definitions
- the present invention is excellent in flexibility and gas barrier properties. By using this as the innermost layer of a refrigerant transport hose, refrigerant transport excellent in gas barrier properties (refrigerant permeation resistance), dynamic durability, and flexibility is achieved.
- the present invention relates to a polyamide-based composite resin capable of providing a hose for use.
- the present invention also relates to a hose for transporting refrigerant.
- the present invention relates to a refrigerant transporting hose suitable as a piping hose for a car cooler or an air conditioner for an automobile, and particularly excellent in gas barrier properties (refrigerant permeability) and dynamic durability.
- the present invention relates to a hose for transporting a refrigerant which has excellent properties and flexibility.
- the high-pressure line is a line that supplies high-temperature refrigerant, which has been compressed by the compressor into a gas-liquid mixed state, to the condenser at high pressure.
- the low-pressure line is a line for returning low-pressure / low-temperature refrigerant vaporized by the evaporator to the compressor.
- Refrigerant transport hoses have excellent gas barrier properties that can reliably prevent leakage of refrigerant (freon), and flexibility for ensuring the refrigerant transport hoses can be drawn around in narrow spaces.
- properties such as aging resistance, impact resistance, and mechanical strength are required.However, regarding gas barrier properties, the amount of refrigerant leakage in high-pressure lines is remarkably mechanical. There is a demand for high gas barrier properties.
- the conventional hose for transporting refrigerant is a composite resin obtained by adding a polyolefin as a flexibility-imparting agent to a polyamide resin such as polyamide 6 (nylon 6).
- the innermost layer is formed as a gas barrier layer, and has a multilayer structure in which a rubber layer is covered on the outer periphery.
- the gas barrier property of the polyolefin itself is inferior to that of the polyamide, so that the gas barrier property of the innermost layer made of the composite resin is impaired.
- the present applicant firstly excels in gas nori- ness and flexibility.
- the innermost layer contains polyamide 6: 58-72 parts by weight and polyolefin: 42-28 parts by weight
- the sea phase is polyamide 6
- the island phase is polyolefin
- the polyolefin is We have proposed a hose for transporting refrigerant, which is composed of a resin layer having a sea-island structure in which polyamide 6 is dispersed in the island phase in a scattered manner (Japanese Patent Application Laid-Open No. 2000-120944).
- the polyolefin island phase is smaller than the original volume of polyolefin.
- the apparent volume fraction is increased by the amount of the polyamide 6 phase present inside.
- the apparent volume fraction of the island phase of polyolefin is increased, the same effect of improving the flexibility-imparting effect as in the case of increasing the blending amount of polyolefin is obtained.
- the actual blending amount of polyolefin is kept low, and therefore, it is possible to obtain a good effect of improving flexibility without causing a decrease in gas barrier properties due to blending of polyolefin.
- the present invention relates to a polyamide-based composite resin having excellent gas barrier properties, sufficiently excellent flexibility and durability, and capable of forming a good gas barrier layer of a refrigerant transport hose.
- An object of the present invention is to provide a refrigerant transport hose using a resin.
- the polyamide-based composite resin of the first aspect is a polyamide-based composite resin containing a polyamide and a polyolefin, wherein the polyamide is a polyamide having meta-xylenediamine as a structural unit.
- polyamide MX (Hereinafter sometimes referred to as “polyamide MX”).
- a polyamide-based composite resin obtained by adding a polyolefin as a flexibility-imparting agent to polyamide MX to form a polymer alloy can realize a polyamide-based composite resin having excellent gas barrier properties, flexibility, and durability.
- the refrigerant transport hose of the second aspect has a resin layer mainly composed of polyamide containing metaxylenediamine as a constituent unit.
- the refrigerant transport hose of the second aspect is made of the polyamide-based composite resin of the first aspect. Layer.
- the refrigerant transport hose of the third aspect is similar to a refrigerant transport hose having at least one resin layer, and the resin is made of a resin mainly composed of polyamide having metaxylene diamine as a structural unit. It is characterized by the following.
- the refrigerant transport hoses of the second and third aspects have excellent gas barrier properties, flexibility, and durability.
- FIG. 1 is a perspective view showing one embodiment of a refrigerant transport hose of a second aspect.
- FIGS. 2a and 2b are perspective views showing another embodiment of the resin layer of the refrigerant transport hose according to the second aspect.
- FIG. 3 is a perspective view showing an embodiment of a refrigerant transport hose of a third aspect.
- the polyamide-based composite resin of the first aspect is a polymer alloy obtained by adding polyolefin as a flexibility-imparting agent to a polyamide having metaxylenediamine as a structural unit.
- a polyamide having meta-xylenediamine as a structural unit is represented, for example, by the following structural formula.
- the polyamide that constitutes the resin of the first aspect may be a homopolymer composed of only metaxylenediamine, or a copolymer of metaxylenediamine and other monomers. It may be. In the case of a copolymer, it is desirable that meta-xylene diamine is contained at preferably 60% by weight or more.
- the present inventors collectively refer to these homopolymers and copolymers as polyamide MX.
- Polyolefins for use as polymer alloys include EPR (ethylene-propylene copolymer), EPDM (ethylene-propylene-gen terpolymer), ionomers, polyolefin copolymers, and IR (isoprene rubber). ), SEBS (styrene-ethylene-butylene-styrene copolymer), halogenated isobutylene-para-methylstyrene copolymer, modified ethylene-acrylic acid, modified ethylene-ethyl acrylate copolymer, and its acid-modified product. And mixtures containing these as main components.
- an acid anhydride such as maleic anhydride
- an alkyl acrylate such as glycidyl methacrylate
- a force modified with epoxy or a modified product thereof etc.
- An alloy structure can be obtained, which is preferable.
- the content in the polyamide-based composite resin is preferably 10 to 40% by weight, particularly preferably 20 to 30% by weight. If the content of polyolefin in the polyamide-based composite resin exceeds 40% by weight, the sea phase and the island phase are reversed in the sea-island structure described later, and the gas barrier property is unpreferably reduced.
- the polyolefin such as an acid-modified polyolefin
- a large amount of the modified polyolefin causes gelling of the resin, and when extruded, causes poor appearance such as roughened skin or fishy appearance.
- the content in the polyamide-based composite resin is preferably 30% by weight or less, for example, 525% by weight.
- the ratio of the polyamide phase dispersed in the island phase of polyolefin to the polyamide (the sum of the polyamide constituting the sea phase and the polyamide phase dispersed in the island phase of polyolefin) (hereinafter, referred to as The ratio is referred to as the “scattering ratio in the form of dots.”) Is preferably about 2.5 to 30% by weight. If this ratio is less than 2.5% by weight, the effect of having the polyamide phase dispersed in the polyolefin island phase cannot be sufficiently obtained. Conversely, if it exceeds 30% by weight, the sea phase cannot be obtained. There is a possibility that the polyamide phase may become too small and the gas barrier properties may be reduced.
- the size of the polyolefin island phase and the size of the polyamide phase in the polyolefin island phase are approximately 0.4-1.5 zm for the polyolefin island phase and 0.05 for the polyamide phase. It is preferably about 0.5 zm.
- the polyamide of the polyamide-based composite resin of the first aspect does not necessarily have to be a polyamide having metaxylenediamine as a structural unit, but a polyamide such as polyamide 6 other than a polyamide having metaxylenediamine as a structural unit. Although it may be contained, in such a case, it is preferable that 51% by weight or more of the total polyamide component in the polyamide-based composite resin be a S-meta-xylene diamine component in order to ensure gas barrier properties.
- Additives such as an antioxidant and an oxidative deterioration agent may be added to the polyamide-based composite resin of the first aspect as needed.
- the polyamide-based composite resin of the first aspect particularly a polyamide-based composite resin having a morphology of sea-island structure as described above, can be produced, for example, by the following method i or ii.
- FIG. 1 is a perspective view showing an embodiment of a refrigerant transport hose of the second aspect
- FIGS. 2a and 2b are perspective views showing another embodiment of a resin layer of the refrigerant transport hose.
- an inner pipe layer 3 composed of a resin layer 1 and an inner pipe rubber layer 2 is covered with an outer rubber 5 via an intermediate rubber layer 4 containing a reinforcing yarn. It is configured. If necessary, an adhesive layer may be provided between the resin layer 1 and the inner pipe rubber layer 2.
- the resin layer 1 is made of the above-described polyamide-based composite resin of the first aspect.
- the thickness of the resin layer 1 is preferably as thick as possible in terms of gas barrier properties and durability of the hose. However, when the thickness is large, flexibility of the hose is sacrificed. Therefore, the thickness of the resin layer 1 is preferably 30 to 300 ⁇ m, particularly 50 to 200 ⁇ m.
- the resin layer 1 even in a single-layer structure, enhances the durability of the refrigerant transport hose, such as the impulse resistance after long-term thermal aging, the vibration durability test after the impulse test, and the dynamic durability test after thermal aging. And further enhance gas barrier performance.
- the hose for transporting refrigerant having the single-layer resin layer 1 is manufactured without co-extrusion to form a multilayer structure.
- the resin layer is not limited to a single-layer structure.
- the resin layer may be the laminated resin layers 1A and 1B shown in FIGS. 2a and 2b.
- an inner tube rubber layer 2 On the laminated resin layers 1A and 1B, an inner tube rubber layer 2, an intermediate rubber layer 4 and a jacket rubber 5 are further formed in the same manner as in FIG.
- the laminated resin layer 1A in FIG. 2A has a three-layer structure in which a layer 11 made of a first resin, a layer 12 made of a second resin, and a layer 13 made of a first resin are laminated in this order from the inside. It is.
- the laminated resin layer 1B shown in FIG. 2B includes, from the inside, a layer 21 made of the first resin, a layer 22 made of the second resin, a layer 23 made of the first resin, a layer 24 made of the second resin, This is a structure composed of five layers laminated in the order of a layer 25 composed of one resin.
- the layers 11, 13, 21, 23, and 25 made of the first resin are layers mainly responsible for durability and flexibility, and are preferably 58 to 72 parts by weight of polyamide 6 and 42 to 28 parts by weight of polyolefin. (But the total amount of polyamide 6 and polyolefin is 100 parts by weight), and the polyolefin island phase is dispersed in the polyamide 6 sea phase, and the polyamide 6 is contained in the polyolefin island phase. It is composed of a polyamide 6_polyolefin-based composite resin having a structure dispersed in a scattered manner.
- the gas barrier properties will be inferior even if the morphology has the specific sea-island structure described above. Conversely, if the amount of polyamide 6 is more than 72 parts by weight, the morphology of the above-mentioned specific sea-island structure is inferior to flexible 1 "raw material. [0041] Even if the polyamide 6-polyolefin-based composite resin does not exhibit the above-mentioned sea-island structure morphology even in the above-mentioned polyamide 6-polyolefin composition range, good gas barrier properties and flexibility are obtained. I can't.
- polyamide 6 the total of polyamide 6 constituting the sea phase and polyamide 6 phase which is scattered in the island phase of polyolefin.
- the proportion of the polyamide 6 phase present in the form of scattered spots in the island phase of polyolefin with respect to) (hereinafter referred to as the “scattered spot rate”) is preferably about 2.5 to 30% by weight. . If this ratio is less than 2.5% by weight, the above-mentioned effects of the presence of the polyamide 6 phase in the form of scattered points in the polyolefin island phase cannot be sufficiently obtained. Conversely, if this ratio exceeds 30% by weight, There is a possibility that the gas nori property may be reduced due to too little polyamide 6 phase as the sea phase.
- the size of the polyolefin island phase and the size of the polyamide 6 phase in the polyolefin island phase are approximately 0.4-1.5 microns, and the size of the polyamide 6 phase is 0. .05-0. Preferably about 5 microns.
- polyolefins examples include EPR (ethylene-propylene copolymer), EPDM (ethylene-propylene-gen terpolymer), ionomer, ⁇ -olefin copolymer, IR (isoprene rubber), and SEBS (styrene-styrene copolymer).
- EPR ethylene-propylene copolymer
- EPDM ethylene-propylene-gen terpolymer
- ionomer ⁇ -olefin copolymer
- IR isoprene rubber
- SEBS styrene-styrene copolymer
- Ethylene-butylene-styrene copolymer halogenated isobutylene-para-methylstyrene copolymer, ethylene-acrylic acid-modified product, ethylene-ethyl acrylate copolymer, and its acid-modified product, and their main components And the like.
- the polyamide 6-polyolefin-based composite resin may be added with additives such as an antioxidant and an oxidation-deteriorating agent, if necessary.
- the above-mentioned composite resin having a sea-island structure morphology is prepared, for example, by kneading polyamide 6 and polyolefin at a predetermined mixing ratio to form a master batch, and then mixing the master batch with polyamide 6 Can be produced by kneading.
- the composite resin can also be produced by melt-kneading the polyamide 6 and polyolefin blend by high shear.
- the layers 12, 22, and 24 made of the second resin are layers mainly responsible for gas barrier properties, and are made of the first polyamide composite resin.
- the thickness of each of the first resin layers 11 and 13 is about 200 / im
- the thickness of the second resin layer 12 is about 100 / im. im as well.
- the first resin layers 21 and 25 each have a thickness of about 100 / m
- the first resin layer 23 has a thickness of about 200 zm.
- the thickness of each of the resin layers 22 and 24 may be about 50 Atm.
- the laminated resin layers 1A and IB can be easily produced by integral molding by co-extrusion of these plural resin layers.
- the layer made of the first resin and the layer made of the second resin are both made of polyamide as a base resin, and because of their good compatibility, they are firmly bonded by co-extrusion. There is no need to perform any special bonding treatment on them.
- refrigerant transport hose of the second aspect may be the same as ordinary refrigerant transport hoses.
- the rubber constituting the inner pipe rubber layer 2 and the outer cover rubber 5 is generally butyl rubber (IIR), chlorinated butyl rubber (C1-1R), chlorine Polyethylene, chlorosulfonated polyethylene, brominated butyl rubber (Br-IIR), isobutylene-bromoparamethylstyrene copolymer, EPR (ethylene-propylene copolymer), EPDM (ethylene-propylene-gen terpolymer) ), NBR (acrylonitrile butadiene rubber), CR (chloroprene rubber), hydrogenated NBR, acrylic rubber, blends of two or more of these rubbers, or blends with polymers based on these rubbers
- butyl rubber or EPDM rubber is used.
- Compounding formulas such as fillers, processing aids, antioxidants, vulcanizing agents and vulcanization accelerators which are commonly used can be applied to these rubbers.
- the rubber type of the inner rubber layer 2 and the rubber type of the outer rubber 5 may be the same or different.
- the rubber of the intermediate rubber layer 4 is not particularly limited as long as it has good adhesion to the inner tube rubber layer 2 and the outer rubber 5.
- the reinforcing yarn may be a commonly used one.
- the reinforcing yarns are polyester, wholly aromatic polyester, nylon-vinylon, rayon, aramide, polyarylate, polyethylene naphthalate. And twisted yarns thereof.
- the inner tube rubber layer 2 preferably has a thickness of 0.8-4 mm in order to make itself flexible.
- the thickness of the intermediate rubber layer 4 including the reinforcing yarn is preferably about 0.5 to 5 mm, and the thickness of the outer rubber layer 5 is preferably about 1 to 2 mm.
- the refrigerant transport hose of the second aspect is prepared by extruding and laminating the materials of the respective constituent layers to a predetermined thickness on a mandrel and vulcanizing them at 140 to 170 ° C for 30 to 120 minutes according to a conventional method. Can manufacture power S.
- Tables 13 to 13 below show the rubber mixing ratios of Example 16 and Comparative Examples 14 to 14, and the rubber layers of the inner rubber layer, the intermediate rubber layer, and the outer rubber layer.
- a refrigerant transport hose having the configuration shown in FIG. 1 was manufactured in the following procedure.
- Polyamide MX MX nylon ⁇ S6001 '' manufactured by Mitsubishi Gas Chemical Company
- Polyolefin ⁇ -olefin polymer “Tuffmer A-1050” manufactured by Mitsui Chemicals, Inc.
- Acid-modified polyolefin maleic acid-modified ⁇ -olefin polymer “Tuffmer 7010” manufactured by Mitsui Chemicals, Inc.
- Polyamide 6 nylon "1022 ⁇ ” manufactured by Ube Industries, Ltd.
- a resin layer 1 having a thickness of 150 ⁇ m was formed by extrusion with a resin composition shown in Table 4 on a mandrel having a diameter of 11 mm, and then the inner rubber layer shown in Table 1 was extruded to a thickness of 1.2 mm. Twenty-four 3,000-denier polyester reinforcing yarns are aligned and spirally wound on this, and the intermediate rubber shown in Table 2 is extruded on this reinforcing yarn layer to a thickness of 0.3 mm. Twenty-four polyester reinforcing yarns were aligned and spirally wound in the opposite direction. Next, a jacket rubber shown in Table 3 was extruded thereon to a thickness of 1.3 mm and vulcanized at 150 ° C for 90 minutes to obtain a refrigerant transport hose.
- the obtained hose for transporting refrigerant was examined for flexibility, dynamic durability and gas barrier properties by the following methods, and was determined to be extremely good (VWG), excellent (VVG), good (VG), good and ordinary.
- VWG extremely good
- VVG excellent
- VG good
- BB extremely poor
- the polyolefin island phase having a diameter of about 0.5 to 2.0 / im was dispersed in the sea phase of polyamide MX, and the polyolefin island phase was dispersed.
- polyamide MX having a diameter of about 0.04-0.45 ⁇ was dispersed in the form of scattered points, and the scattered point ratio obtained from transmission electron microscope images is as shown in Table 4. there were.
- the load was measured when the hose was wound around the mandrel with a radius of 100 mm for half a turn.
- the resin layer formed by co-extrusion was a laminated resin layer 1A having a three-layer structure of the following formulation A / formulation B / formulation A, as shown in Fig. 2a, and the thickness of each layer was as shown in Table 5.
- a refrigerant transport hose was manufactured in the same manner as in Example 1 and evaluated in the same manner. The results are shown in Table 5.
- Formulation A Polyamide 6 seaweed phase obtained by kneading 72% by weight of polyamide 6 (“1022B” manufactured by Ube Industries, Ltd.) and 28% by weight of polyolefin (“Tuffmer MH5010” manufactured by Mitsui Chemicals, Inc.) Resin in which the island phase is dispersed, the dispersed particle size is 0.5 to 1.5 zm, and the dispersed ratio in the form of dots is 5.1% by weight
- Formula B Polyamide MX (S6001 manufactured by Mitsubishi Gas Chemical) and 80% by weight of polyolefin (Tuffmer MH5010 manufactured by Mitsui Chemicals) kneaded with 20% by weight. Is dispersed, the dispersed particle size is 0.5-1.5 zm, Is 5.1% by weight resin.
- a refrigerant transport hose was manufactured in the same manner as in Example 6, except that the resin layer was the only layer 11 made of the first resin, and the same evaluation was performed. The results are shown in Table 5.
- the hose for transporting refrigerant using the polyamide-based composite resin of the present invention exhibits excellent gas barrier properties, especially when used in a high-pressure line, and has flexibility and dynamic durability. You can see that it is also excellent.
- the refrigerant transport hose 30 of the third aspect will be described with reference to FIG.
- the refrigerant transport hose 30 has a layer 31 composed of a laminated resin and an inner tube layer 33 composed of an inner tube rubber layer 32, an intermediate rubber layer 34 containing a reinforcing thread, and a jacket rubber 35. Note that an adhesive layer may be provided between the laminated resin layer 31 and the inner tube rubber layer 32 as necessary.
- the laminated resin layer 31 is mainly composed of the innermost layer 31a made of the first resin, which mainly has durability and flexibility, and the layer composed of the second resin mainly made of the gas barrier, which is laminated on the outer periphery thereof. 31b.
- the resin suitable for the layer 31a made of the first resin is the same as the resin of the first resin layers 11, 13, 21, 23, and 25 of the second aspect. Is done.
- the metaxylenediamine of polyamide having metaxylenediamine as a structural unit, which is the main component of the layer 31b made of the second resin, is the polyamide MX described in the first aspect. Everything about polyamide MX in the first aspect applies here.
- the layer 31b made of the second resin may be composed of only the polyamide MX, and in this case, extremely excellent gas barrier properties can be obtained. Further, the layer lb made of the second resin has a polyamide alloy as a main component and other components, for example, polyolefin which acts as a flexibility-imparting agent is added to form a polymer alloy to form a polymer alloy. It may be a polyamide-based composite resin. All of the description of the polyamide-based composite resin of the first aspect applies here.
- the thickness of the layer 31a made of the first resin is preferably as thick as possible in terms of the durability performance of the hose. Thickening sacrifices flexibility as a hose. Therefore, the thickness of the layer 31a made of the first resin is preferably 50 to 500 ⁇ m, particularly 100 to 300 ⁇ m.
- the thickness of the layer 31b composed of the polyamide MX or made of the second resin containing the polyamide MX as a main component is preferably as thick as possible in terms of gas barrier performance. It greatly sacrifices the flexibility and durability of the hose. Therefore, the thickness of the second resin by Li Cheng layer 31b is 10- 200 beta m, it forces S preferably les is particularly 20- 100 mu m,.
- the laminated resin layer 31 composed of the layer 31a made of the first resin and the layer 31b made of the second resin is not necessarily the layer 31a made of the first resin and the layer 31b made of the second resin. It is not necessary for the hose to have a two-layer laminated structure in which each layer is laminated one by one, as long as the overall thickness of the hose is not excessively increased and the flexibility is not reduced, and the cost and weight are not increased. It may have a laminated structure of three or more layers. For example, a laminated structure as shown in FIGS. 2a and 2b may be adopted.
- the multilayer resin layers 31, 1A, and IB having such a multilayer structure can be easily manufactured by integral molding by co-extrusion of these resin layers.
- Both the layer made of the first resin and the layer made of the second resin are based on polyamide. Since it is a fat and has good compatibility with both, it is firmly bonded by co-extrusion. Therefore, it is not necessary to separately perform special bonding treatment between layers.
- the configuration of the refrigerant transport hose of Fig. 1 can be employed.
- the material and thickness of the inner tube rubber layer 32, the intermediate rubber layer 34, and the outer rubber 35 are described in terms of the material and thickness of the inner tube rubber layer 2, the intermediate rubber layer 4, and the outer rubber 5. Applied.
- the description of the method of manufacturing the refrigerant transport hose 10 applies to the refrigerant transport hose 30.
- the third aspect will be described more specifically with reference to examples and comparative examples, but the third aspect is not limited to the following examples as long as the gist of the third aspect is not exceeded.
- composition of the inner rubber layer used in the following Examples and Comparative Examples is as shown in Table 6.
- composition of the intermediate rubber layer and the outer rubber layer is as shown in Tables 2 and 3 above.
- a refrigerant transport hose having the configuration shown in FIG. 3 was manufactured by the following procedure.
- the inner rubber layer shown in Table 6 was extruded to a thickness of 1.2 mm. Twenty-four 3,000-denier polyester reinforcing yarns are wrapped around this and spirally wound, and the intermediate rubber shown in Table 2 is extruded on this reinforcing yarn layer to a thickness of 0.3 mm, and then 3,000 denier Twenty-four polyester reinforcing yarns were aligned and spirally wound in the opposite direction. Next, a jacket rubber shown in Table 3 was extruded thereon to a thickness of 1.3 mm and vulcanized at 150 ° C for 90 minutes to obtain a refrigerant transport hose.
- the polyamide 6-polyolefin-based composite resin (hereinafter, referred to as "formulation A") in the layer composed of the first resin has a polyolefin island phase dispersed in a polyamide 6 sea phase.
- Polyamide 6 was dispersed in the polyolefin island phase in the form of dispersed particles having a dispersed particle size of 0.5-1.5 ⁇ , and the dispersed ratio determined by a transmission electron microscope image was 5.1% by weight. %Met.
- Example 7 a refrigerant transport hose was manufactured in the same manner as in Example 7 except that the thickness of the first resin layer 31a and the second resin layer 31b was as shown in Table 7, and the same evaluation was performed. The results are shown in Table 7.
- a refrigerant transport hose was manufactured in the same manner as in Example 7, except that the layer 31a made of the first resin was not formed and the thickness of the layer 31b made of the second resin was as shown in Table 7. The evaluation was performed in the same manner, and the results are shown in Table 7.
- Example 7 The same procedure as in Example 7 was carried out except that the resin layer formed by co-extrusion was a laminated resin layer having a three-layer structure of Formula A / Formula B / Formula A described above and the thickness of each layer was as shown in Table 7.
- a hose for transporting refrigerant was manufactured in the same manner as above, and the same evaluation was performed. The results are shown in Table 7.
- Formula B Polyamide MX (S6001 manufactured by Mitsubishi Gas Chemical) and 80% by weight of polyolefin (Tuffmer MH5010 manufactured by Mitsui Chemicals) kneaded with 20% by weight. Resin in which the island phase is dispersed, the dispersed particle size is 0.5-1.5 / im, and the dot dispersion ratio is 5.1% by weight.
- Example 7 a refrigerant transport hose was manufactured in the same manner except that the layer made of the second resin was not formed, and only the layer 31a made of the first resin was formed. Table 7 shows the results.
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- Rigid Pipes And Flexible Pipes (AREA)
Abstract
Description
Claims
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JP2004104947 | 2004-03-31 | ||
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JP2004-299025 | 2004-10-13 | ||
JP2004299025A JP2006002130A (ja) | 2004-05-17 | 2004-10-13 | ポリアミド系複合樹脂及び冷媒輸送用ホース |
JP2004299024A JP2005315406A (ja) | 2004-03-31 | 2004-10-13 | 冷媒輸送用ホース |
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Cited By (4)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
EP1886810A1 (en) * | 2006-07-14 | 2008-02-13 | Nitta Moore Company | Tube |
JP2012207797A (ja) * | 2009-03-27 | 2012-10-25 | Bridgestone Corp | 冷媒輸送用ホース及びそのガスバリア層形成用ポリアミド樹脂組成物 |
WO2018123120A1 (ja) * | 2016-12-27 | 2018-07-05 | 住友理工株式会社 | 冷媒輸送用ホース |
US10421860B2 (en) | 2014-12-26 | 2019-09-24 | Mitsubishi Gas Chemical Company, Inc. | Thermoplastic resin composition and molded body comprising the same |
Citations (7)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPH08247345A (ja) * | 1995-03-09 | 1996-09-27 | Elf Atochem Sa | ポリアミドをベースとしたガソリン移送用パイプ |
JPH1158490A (ja) * | 1997-08-13 | 1999-03-02 | Unitika Ltd | 多層延伸ポリアミドフィルムの製造方法 |
JP2000120944A (ja) * | 1998-10-16 | 2000-04-28 | Bridgestone Corp | 冷媒輸送用ホース |
JP2000220770A (ja) * | 1999-02-03 | 2000-08-08 | Nichirin Co Ltd | 複合フレキシブルホース |
JP2001002918A (ja) * | 1999-06-18 | 2001-01-09 | Toyobo Co Ltd | ポリアミド樹脂組成物 |
JP2002254581A (ja) * | 2000-12-26 | 2002-09-11 | Ube Ind Ltd | ポリアミド積層二軸延伸フィルム |
JP2002370273A (ja) * | 2001-05-30 | 2002-12-24 | Goodyear Tire & Rubber Co:The | 冷媒ホース |
-
2005
- 2005-03-22 WO PCT/JP2005/005096 patent/WO2005097903A1/ja active Application Filing
Patent Citations (7)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPH08247345A (ja) * | 1995-03-09 | 1996-09-27 | Elf Atochem Sa | ポリアミドをベースとしたガソリン移送用パイプ |
JPH1158490A (ja) * | 1997-08-13 | 1999-03-02 | Unitika Ltd | 多層延伸ポリアミドフィルムの製造方法 |
JP2000120944A (ja) * | 1998-10-16 | 2000-04-28 | Bridgestone Corp | 冷媒輸送用ホース |
JP2000220770A (ja) * | 1999-02-03 | 2000-08-08 | Nichirin Co Ltd | 複合フレキシブルホース |
JP2001002918A (ja) * | 1999-06-18 | 2001-01-09 | Toyobo Co Ltd | ポリアミド樹脂組成物 |
JP2002254581A (ja) * | 2000-12-26 | 2002-09-11 | Ube Ind Ltd | ポリアミド積層二軸延伸フィルム |
JP2002370273A (ja) * | 2001-05-30 | 2002-12-24 | Goodyear Tire & Rubber Co:The | 冷媒ホース |
Cited By (6)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
EP1886810A1 (en) * | 2006-07-14 | 2008-02-13 | Nitta Moore Company | Tube |
JP2012207797A (ja) * | 2009-03-27 | 2012-10-25 | Bridgestone Corp | 冷媒輸送用ホース及びそのガスバリア層形成用ポリアミド樹脂組成物 |
US10421860B2 (en) | 2014-12-26 | 2019-09-24 | Mitsubishi Gas Chemical Company, Inc. | Thermoplastic resin composition and molded body comprising the same |
WO2018123120A1 (ja) * | 2016-12-27 | 2018-07-05 | 住友理工株式会社 | 冷媒輸送用ホース |
JPWO2018123120A1 (ja) * | 2016-12-27 | 2019-07-11 | 住友理工株式会社 | 冷媒輸送用ホース |
US10514114B2 (en) | 2016-12-27 | 2019-12-24 | Sumitomo Riko Company Limited | Hose for transporting refrigerant |
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