US20110155359A1 - Hollow structures and associated method for conveying refrigerant fluids - Google Patents

Hollow structures and associated method for conveying refrigerant fluids Download PDF

Info

Publication number
US20110155359A1
US20110155359A1 US12/963,772 US96377210A US2011155359A1 US 20110155359 A1 US20110155359 A1 US 20110155359A1 US 96377210 A US96377210 A US 96377210A US 2011155359 A1 US2011155359 A1 US 2011155359A1
Authority
US
United States
Prior art keywords
group
acid
carbon atoms
resin composition
hollow structure
Prior art date
Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
Abandoned
Application number
US12/963,772
Other languages
English (en)
Inventor
Shailesh Ratilal Doshi
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
EIDP Inc
Original Assignee
EI Du Pont de Nemours and Co
Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)
Filing date
Publication date
Application filed by EI Du Pont de Nemours and Co filed Critical EI Du Pont de Nemours and Co
Priority to US12/963,772 priority Critical patent/US20110155359A1/en
Publication of US20110155359A1 publication Critical patent/US20110155359A1/en
Abandoned legal-status Critical Current

Links

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
    • B32B27/00—Layered products comprising a layer of synthetic resin
    • B32B27/06—Layered products comprising a layer of synthetic resin as the main or only constituent of a layer, which is next to another layer of the same or of a different material
    • B32B27/08—Layered products comprising a layer of synthetic resin as the main or only constituent of a layer, which is next to another layer of the same or of a different material of synthetic resin
    • 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
    • B32B27/32—Layered products comprising a layer of synthetic resin comprising polyolefins
    • 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
    • B—PERFORMING OPERATIONS; TRANSPORTING
    • B60—VEHICLES IN GENERAL
    • B60H—ARRANGEMENTS OF HEATING, COOLING, VENTILATING OR OTHER AIR-TREATING DEVICES SPECIALLY ADAPTED FOR PASSENGER OR GOODS SPACES OF VEHICLES
    • B60H1/00—Heating, cooling or ventilating [HVAC] devices
    • B60H1/00507—Details, e.g. mounting arrangements, desaeration devices
    • B60H1/00557—Details of ducts or cables
    • B60H1/00571—Details of ducts or cables of liquid ducts, e.g. for coolant liquids or refrigerants
    • 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
    • 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 relates to the field of flexible hollow structures that are particularly suitable for conveying refrigerant fluids.
  • Hollow structures made of thermoplastic are well known for a variety of applications, like for example in the building industry for water pipes, radiator pipes or floor-heating pipes or in automotive conduits to carry many different fluids or liquid media, and are desired to display a balance of properties including thermal, mechanical and chemical resistance.
  • structures made of thermoplastic materials and used to convey fluids such structures (pipes, ducts, conduits, tubes, tubings, etc.) are desired to exhibit good mechanical properties, flexibility, impermeability and chemical resistance to the fluid(s) being conveyed.
  • the refrigerant fluid needs to be transported through and/or between various components of the system such as the compressor, condenser and evaporator.
  • Hollow structures used to convey refrigerant fluids are required to exhibit a balance of properties including flexibility, thermal, mechanical and chemical resistance to all of the constituents of the refrigerant fluid.
  • Such structures need to be flexible for ease of installation and use, and often must be shaped into curves and bends for connecting components already installed into fixed positions without kinking.
  • Such structures need to have a high resistance to bursting pressures and possess high impermeability to the refrigerant fluid being conveyed. It is important that the structure not suffer from deterioration leading to the loss of properties upon long term contact with the refrigerant fluid. For example, a reduction in molecular weight and concomitant loss in physical properties can result in failure of the structure during use. Such failure can be catastrophic, with the loss of refrigerant fluid causing the impairment of the performance of the device within which the hollow structure is incorporated.
  • the layers of such structures often comprise dissimilar materials to satisfy specified performance criteria by placing different materials at the most appropriate position in the structure.
  • the multilayer hollow structure may comprise one or more barrier layers made of a thermoplastic resin that possess high impermeability to the refrigerant fluid, one or more elastomeric layers to provide flexibility, one or more layers of braiding to provide burst strength to withstand the refrigerant fluid pressure, and adhesive layers disposed between any of these layers to provide adhesion.
  • Polyamides are a desirable material to use for hoses and pipes because they have good chemical resistance, good physical properties, and can be conveniently formed into hoses with a variety of diameters and incorporated into multilayered hoses.
  • These polyamides may further comprise plasticizers and/or toughening agents.
  • European Pat. No. 0,945,660 discloses a multilayer hose comprising an innermost layer comprising a polyamide, especially polyamide 6, and optionally a polyolefin rubber, an intermediate reinforcing layer made of aramid fibers and an outermost layer made of an ethylene acrylic rubber.
  • a hollow structure for conveying a refrigerant fluid comprising a layer made of a resin composition comprising one or more semi-aromatic polyamides and one or more functionalized polyolefins,
  • the one or more semi-aromatic polyamides are selected from copolyamides made from: a) group A monomers selected from:
  • fluid refers to a substance that flows and conforms to the outline of its container, a fluid can be a liquid or a gas.
  • pipe used interchangeably herein to denote a hollow structure, i.e. any structure having an empty or concave interior part used to convey a fluid.
  • the hollow structure according to the present invention comprises a layer made of a resin composition comprising one or more semi-aromatic polyamides and one or more functionalized polyolefins.
  • the one or more semi-aromatic polyamides comprised in the resin composition described herein are selected from copolyamides made from:
  • Suitable aromatic dicarboxylic acids having 8 to 20 carbon atoms include terephthalic acid, isophthalic acid, phthalic acid, 2-methyl terephthalic acid, diphenic acid, 1,5-naphthalenedicarboxylic acid, 2,6-naphthalenedicarboxylic acid, and 2,7-naphthalenedicarboxylic, 1,5-nathphalenedicarboxylic acid; 2,6-nathphalenedicarboxylic acid; terephthalic acid and isophthalic acid being preferred.
  • Suitable aliphatic dicarboxylic acids having 6 to 20 carbon atoms include adipic acid (C6), pimelic acid (C7), suberic acid (C8), azelaic acid (C9), decanedioic acid (C10), undecanedioic acid (C11), dodecanedioic acid (C12), tridecanedioic acid (C13), tetradecanedioic acid (C14), and pentadecanedioic acid (C15), hexadecanoic acid (C16), octadecanoic acid (C18) and eicosanoic acid (C20).
  • adipic acid C6
  • pimelic acid C7
  • suberic acid C8
  • azelaic acid C9
  • decanedioic acid C10
  • undecanedioic acid C11
  • dodecanedioic acid C12
  • Suitable aliphatic diamines having 4 to 20 carbon atoms include tetramethylene diamine, hexamethylene diamine, octamethylene diamine, nonamethylenediamine, decamethylene diamine, dodecamethylene diamine, 2-methylpentamethylene diamine, 2-ethyltetramethylene diamine, 2-methyloctamethylene diamine, trimethylhexamethylene diamine, and bis(p-aminocyclohexyl)methane.
  • Suitable aromatic diamines having 6 to 20 carbon atoms include m-xylylenediamine and p-xylylenediamine.
  • Suitable aromatic aminocarboxylic acids having 7 to 20 carbon atoms include p-aminobenzoic acid, m-aminobenzoic acid, anthranilic acid 6-amino-2-naphthoic acid.
  • Suitable lactams include caprolactam and laurolactam.
  • a suitable aliphatic aminocarboxylic acid includes 11-aminoundecanoic acid.
  • the one or more semi-aromatic polyamides comprised in the resin composition described herein are selected from copolyamides made from:
  • the one or more semi-aromatic polyamides are selected from copolyamides made from:
  • group A monomers selected from terephthalic acid and hexamethylenediamine or terephthalic acid and tetramethylenediamine
  • group B monomers selected from adipic acid and tetramethylenediamine; adipic acid and hexamethylenediamine; decanedioic acid and hexamethylenediamine; dodecanedioic acid and hexamethylenediamine; caprolactam; laurolactam; 11-aminoundecanoic acid;
  • group A monomers selected terephthalic acid and decamethylenediamine
  • group B monomers selected from decanedioic acid and decamethylenediamine
  • group A monomers selected adipic acid and m-xylylenediamine
  • group B monomers selected from adipic acid and hexamethylenediamine
  • the one or more semi-aromatic polyamides are selected from copolyamides made from: a) group A monomers selected from terephthalic acid and hexamethylenediamine and b) group B monomers selected from adipic acid and hexamethylenediamine.
  • copolyamides described herein may be prepared by any means known to those skilled in the art, such as in a batch process using, for example, an autoclave or using a continuous process. See, for example, Kohan, M. I. Ed. Nylon Plastics Handbook, Hanser: Kunststoff, 1995; pp. 13-32. Generally, the monomers are allowed to react to form a random chain of interlinked monomers.
  • the resin composition described herein comprises one or more functionalized polyolefins.
  • the one or more functionalized polyolefins may be used alone or may be used in combination with the one or more unfunctionalized polyolefins described below.
  • the term “functionalized polyolefin” refers to an alkylcarboxyl-substituted polyolefin, which is a polyolefin that has carboxylic moieties attached thereto, either on the polyolefin backbone itself or on side chains.
  • carboxylic moiety refers to carboxylic groups, such as carboxylic acids, carboxylic acid ester, carboxylic acid anhydrides and carboxylic acid salts.
  • Functionalized polyolefins may be prepared by direct synthesis or by grafting.
  • An example of direct synthesis is the polymerization of ethylene and/or at least one alpha-olefin with at least one ethylenically unsaturated monomer having a carboxylic moiety.
  • An example of grafting process is the addition of at least one ethylenically unsaturated monomer having at least one carboxylic moiety to a polyolefin backbone.
  • the ethylenically unsaturated monomers having at least one carboxylic moiety may be, for example, mono-, di-, or polycarboxylic acids and/or their derivatives, including esters, anhydrides, salts, amides, imides, and the like.
  • Suitable ethylenically unsaturated monomers include methacrylic acid; acrylic acid; ethacrylic acid; glycidyl methacrylate; 2-hydroxy ethylacrylate; 2-hydroxy ethyl methacrylate; diethyl maleate; monoethyl maleate; di-n-butyl maleate; maleic anhydride; maleic acid; fumaric acid; mono- and disodium maleate; acrylamide; glycidyl methacrylate; dimethyl fumarate; crotonic acid, itaconic acid, itaconic anhydride; tetrahydrophthalic anhydride; monoesters of these dicarboxylic acids; dodecenyl succinic anhydride; 5-norbornene-2,3-anhydride; nadic anhydride (3,6-endomethylene-1,2,3,6-tetrahydrophthalic anhydride); nadic methyl anhydride; and the like.
  • polyolefins are incompatible with polyamides, it is necessary to modify them with functional groups that are capable of reacting with the acid or amine ends of the polyamide polymer. Due to the fact that the reaction of an anhydride with an amine is very fast, anhydrides are preferred grafting agents and more preferably maleic anhydride is chosen.
  • the one or more functionalized polyolefins are one or more grafted polyolefins.
  • the grafting agents i.e. the at least one monomer having at least one carboxylic moiety, is preferably present in the one or more functionalized polyolefins in an amount from at or about 0.05 to at or about 6 weight percent, preferably from at or about 0.1 to at or about 2.0 weight percent, the weight percentages being based of the total weight of the one or more functionalized polyolefins.
  • Grafted polyolefins are preferably derived by grafting at least one monomer having at least one carboxylic moiety to a polyolefin, an ethylene alpha-olefin or a copolymer derived from at least one alpha-olefin and a diene.
  • the resin composition described herein comprises grafted polyolefins selected from grafted polyethylenes, grafted polypropylenes, grafted ethylene alpha-olefin copolymers, grafted copolymers derived from at least one alpha-olefin and a diene and mixtures thereof.
  • the resin composition described herein comprises maleic anhydride grafted polyolefins selected from maleic anhydride grafted polyethylenes, maleic anhydride grafted polypropylenes, maleic anhydride grafted ethylene alpha-olefin copolymers, maleic anhydride grafted copolymers derived from at least one alpha-olefin and a diene and mixtures thereof.
  • Polyethylenes used for preparing maleic anhydride grafted polyethylene are commonly available polyethylene resins selected from HDPE (density higher than 0.94 g/cm 3 ), LLDPE (density of 0.915-0.925 g/cm 3 ) or LDPE (density of 0.91-0.94 g/cm 3 ).
  • Polypropylenes used for preparing maleic anhydride grafted polypropylene are commonly available copolymer or homopolymer polypropylene resins.
  • Ethylene alpha-olefins copolymers comprise ethylene and one or more alpha-olefins, preferably the one or more alpha-olefins have 3-12 carbon atoms.
  • alpha-olefins include but are not limited to propylene, 1-butene, 1-pentene, 1-hexene-1,4-methyl 1-pentene, 1-heptene, 1-octene, 1-nonene, 1-decene, 1-undecene and 1-dodecene.
  • the ethylene alpha-olefin copolymer comprises from at or about 20 to at or about 96 weight percent of ethylene and more preferably from at or about 25 to at or about 85 weight percent; and from at or about 4 to at or about 80 weight percent of the one or more alpha-olefins and more preferably from at or about 15 to at or about 75 weight percent, the weight percentages being based on the total weight of the ethylene alpha-olefins copolymers.
  • Preferred ethylene alpha-olefins copolymers are ethylene-propylene copolymers and ethylene-octene copolymers.
  • Copolymers derived from at least one alpha-olefin and a diene are preferably derived from alpha-olefins having preferably 3-8 carbon atoms.
  • Preferred copolymers derived from at least one alpha-olefin and a diene are ethylene propylene diene elastomers.
  • EPDM ethylene propylene diene elastomers
  • the ethylene propylene diene polymer preferably comprise from at or about 50 to at or about 80 weight percent of ethylene, from at or about 10 to at or about 50 weight percent of propylene and from at or about 0.5 to at or about 10 weight percent of at least one diene, the weight percentages being based on the total weight of the ethylene propylene diene elastomer.
  • the one or more functionalized polyolefins are preferably present in the resin composition described herein in an amount from at or about 5 to at or 40 weight percent and more preferably from at or about 10 to at or 30 weight percent, the weight percentages being based on the total weight of the resin composition.
  • the resin composition described herein may further comprise one or more unfunctionalized polyolefins.
  • the one or more unfunctionalized polyolefins are selected from unfunctionalized polyethylenes, unfunctionalized polypropylenes, unfunctionalized ethylene alpha-olefin copolymers such as those described above, unfunctionalized ethylene propylene diene rubbers (EPDM) such as those described above and mixtures thereof.
  • EPDM unfunctionalized ethylene propylene diene rubbers
  • the one or more unfunctionalized polyolefins are preferably present in the resin composition described herein in an amount from at or about 5 to at or 40 weight percent and more preferably from at or about 10 to at or 30 weight percent, the weight percentages being based on the total weight of the resin composition.
  • the resin composition described herein may further comprise one or more ionomers.
  • Ionomers are thermoplastic resins that contain metal ions in addition to the organic backbone of the polymer such as for example copolymers of an olefin such as ethylene with partially neutralized (from 10 to 99.9%) alpha, beta-unsaturated C 3 -C 8 carboxylic acid.
  • Preferred alpha, beta-unsaturated C 3 -C 8 carboxylic acids are acrylic acid (AA), methacrylic acid (MAA) or maleic acid monoethylester (MAME).
  • Neutralizing agents are alkali metals like lithium, sodium or potassium or transition metals like manganese or zinc.
  • the one or more ionomers are preferably present in the resin composition described herein in an amount from at or about 5 to at or 40 weight percent and more preferably from at or about 10 to at or 30 weight percent, the weight percentages being based on the total weight of the resin composition.
  • Suitable ionomers for use in the present invention are commercially available under the trademark Surlyn® from E. I. du Pont de Nemours and Company, Wilmington, Del.
  • the resin composition described herein may further comprise one or more plasticizers.
  • the one or more plasticizers are selected from sulfonamides, esters of hydroxybenzoic acids, tetrahydrofurfuryl alcohol esters or ethers, esters of citric acid or of hydroxymalonic acid and mixtures thereof.
  • plasticizer examples include without limitation sulfonamides, esters of hydroxybenzoic acids, such as ethyl p-hydroxybenzoate, 2-ethylhexyl para-hydroxybenzoate, octyl p-hydroxybenzoate, 2-decylhexyl para-hydroxybenzoate or isohexadecyl p-hydroxybenzoate; tetrahydrofurfuryl alcohol esters or ethers, such as oligoethoxylated tetrahydrofurfuryl alcohol; esters of citric acid or of hydroxymalonic acid, such as oligoethoxylated malonate.
  • sulfonamides esters of hydroxybenzoic acids, such as ethyl p-hydroxybenzoate, 2-ethylhexyl para-hydroxybenzoate, octyl p-hydroxybenzoate, 2-decylhexyl para-hydroxybenzoate or isohex
  • the one or more plasticizers are sulphonamides and more preferably aromatic sulfonamides such as benzenesulfonamides and toluenesulfonamides.
  • aromatic sulfonamides include N-alkyl benzenesulfonamides and toluenesulfonamides, such as N-butylbenzenesulfonamide (BBSA), N-(2-hydroxypropyl)benzenesulfonamide, N-cyclohexyltoluenesulphonamide; N-n-octyltoluenesulfonamide, N-2-ethylhexylbenzenesulfonamide, N-ethyl-o-toluenesulfonamide, N-ethyl-p-toluenesulfonamide, o-toluenesulfonamide, p-toluenesulfonamide, and the like.
  • BBSA N-butylbenzenesulfonamide
  • BBSA N-(2-hydroxypropyl)benzenesulfonamide
  • Preferred aromatic sulfonamides are N-butylbenzenesulfonamide, N-ethyl-o-toluenesulfonamide, and N-ethyl-p-toluenesulfonamide, are N-butylbenzenesulfonamide being particularly preferred.
  • the one or more plasticizers are preferably present in the resin composition described herein in an amount from at or about 1 to at or 20 weight percent and more preferably from at or about 5 to at or 15 weight percent, the weight percentages being based on the total weight of the resin composition.
  • the plasticizer may be incorporated into the resin composition by melt-blending the polymer with plasticizer and, optionally, other ingredients, or during polymerization.
  • the polyamide monomers are blended with one or more plasticizers prior to starting the polymerization cycle and the blend is introduced to the polymerization reactor.
  • the plasticizer can be added to the reactor during the polymerization cycle.
  • the resin composition described herein may further comprise one or more heat stabilizers.
  • the one or more heat stabilizers are selected from copper salts and/or copper salt derivatives such as for example copper halides or copper acetates; divalent manganese salts and/or derivatives thereof and mixtures thereof.
  • copper salts are used in combination with halide compounds and/or phosphorus compounds and more preferably copper salts are used in combination with iodide or bromide compounds, and still more preferably, with potassium iodide or potassium bromide.
  • the one or more heat stabilizers are preferably present in the resin composition described herein in an amount from at about 0.1 to about 3 weight percent and preferably from at or about 0.1 to at or about 1 weight percent, the weight percentages being based on the total weight of the resin composition.
  • the resin composition described herein may further comprise one or more antioxidants such as phosphorus stabilizers (e.g. phosphate or phosphonite stabilizers), hindered phenol stabilizers, hindered amine stabilizers, aromatic amine stabilizers, thioesters, and phenolic based anti-oxidants that hinder thermally induced oxidation of polymers where high temperature applications are used.
  • the one or more antioxidants are selected from hindered phenol stabilizers, hindered amine stabilizers, phosphorus antioxidants and mixtures thereof.
  • the one or more antioxidants are preferably present in the resin composition described herein in an amount from at or about 0.1 to at or about 3 weight percent and preferably from at or about 0.1 to at or about 1 weight percent, the weight percentages being based on the total weight of the resin composition.
  • the resin composition described herein may further comprise modifiers and other ingredients, including, without limitation, lubricants and mold release agents (including stearic acid, stearyl alcohol and stearamides, and the like), flame retardants, antistatic agents, coloring agents (including dyes, pigments, carbon black, and the like), nucleating agents and other processing aids known in the polymer compounding art.
  • modifiers and other ingredients including, without limitation, lubricants and mold release agents (including stearic acid, stearyl alcohol and stearamides, and the like), flame retardants, antistatic agents, coloring agents (including dyes, pigments, carbon black, and the like), nucleating agents and other processing aids known in the polymer compounding art.
  • the resin composition described herein may further comprise fillers and reinforcing agents such as mineral fillers, glass fibers, nano particulates, carbon fibers, metal fibers and metal-coated fibers.
  • fillers and reinforcing agents such as mineral fillers, glass fibers, nano particulates, carbon fibers, metal fibers and metal-coated fibers.
  • the resin compositions described herein are preferably melt-mixed blends, wherein all of the polymeric components are well-dispersed within each other and all of the non-polymeric ingredients are well-dispersed in and bound by the polymer matrix, such that the blend forms a unified whole. Any melt-mixing method may be used to combine the polymeric components and non-polymeric ingredients of the present invention.
  • the polymeric components and non-polymeric ingredients may be added to a melt mixer, such as, for example, a single or twin-screw extruder; a blender; a single or twin-screw kneader; or a Banbury mixer, either all at once through a single step addition, or in a stepwise fashion, and then melt-mixed.
  • a melt mixer such as, for example, a single or twin-screw extruder; a blender; a single or twin-screw kneader; or a Banbury mixer, either all at once through a single step addition, or in a stepwise fashion, and then melt-mixed.
  • a melt mixer such as, for example, a single or twin-screw extruder; a blender; a single or twin-screw kneader; or a Banbury mixer, either all at once through a single step addition, or in a stepwise fashion, and then melt-mixed.
  • the hollow structures described herein exhibit a good retention of mechanical properties upon exposure to a refrigerant fluid and are therefore particularly suitable in applications where the layer made of the resin composition described herein is in contact with a refrigerant fluid.
  • the hollow structure is preferably in the form of a hose, a pipe, a duct, a tube, tubing or a conduit. Due to the advantages mentioned above, the hollow structures described herein are particularly suitable for use in applications that require conveying a refrigerant fluid or a refrigerant-containing composition.
  • the refrigerant fluid that is conveyed by the hollow structure described herein comprises a hydrofluoroolefin (HFO) and more preferably 2,3,3,3-tetrafluoropropene.
  • HFO hydrofluoroolefin
  • Refrigerants fluids comprising fluorocarbon compounds based on hydrofluoroolefins (HFOs) and especially tetrafluoropropenes (such as for example HFO-1234) are particularly suitable.
  • Hydrofluoroolefins (HFOs) are unsaturated compounds, preferably having at least one double bond, comprising at least one fluorine atom substituent and at least one hydrogen atom.
  • Refrigerant-containing compositions may comprise a variety of optional additives including lubricants (e.g. mineral oil, polyalkylene glycol, polyalkylene glycol ester, polyvinyl ethers, and polyol esters), stabilizers (e.g. dienes, phosphates, phenols and epoxides), metal passivators, corrosion inhibitors, flammability suppressants, and the like.
  • the hollow structure described herein can be circular in cross-section, other shapes including elliptical or other non-circular shapes are also contemplated.
  • the walls of the hollow structure described herein may be smooth or may comprise corrugated regions that are interrupted by smooth regions (hereafter called “partially corrugated hoses”) or can be corrugated all along its length (hereafter called “continuously corrugated hoses”).
  • continuously or partially corrugated hollow structures described herein enable complex routing of the pipes in constrained spaces, such as those available in underhood areas of automobiles and other vehicles.
  • the hollow structure described herein may be manufactured by any melt extrusion process including blow molding, profile extrusion and corrugated extrusion.
  • Profile extrusion and corrugated extrusion are conventional techniques used for manufacturing hollow plastic bodies in arbitrary long lengths.
  • the composition is extruded in a hot moldable state through the gap between the pin and the die of an extrusion head.
  • profile extrusion it is meant a technique used to produce a hollow article having the same cross section over a long length.
  • the pin and die are shaped to produce the desired cross-section, and for example an annular die-gap between concentric circular pin and die is used to make tubes and pipes.
  • the melt may be drawn to a thinner cross section through an air gap.
  • the melt is then cooled and its shape is maintained.
  • corrugated extrusion it is meant a technique used to produce hollow articles comprising corrugated regions that may be interrupted by smooth regions.
  • the pin and the die are positioned inside the two halves of the mold blocks of the equipment.
  • the molten material coming from the extrusion head reaches the mold blocks, it is drawn up to the shape of the mold article either by heated air or by vacuum expansion against the surface of the mold cavity.
  • Such process is described for example in U.S. Pat. Nos. 6,764,627 and 4,319,872 and Intl. Pat. App. Pub. No. WO 03/055664.
  • multilayer hollow structures comprising a layer made of the resin composition described above and one or more additional layers.
  • the layer made of the resin composition described herein may be used as a barrier layer in the hollow structure or as a veneer layer.
  • barrier layer refers to a layer that is not in direct contact with the refrigerant fluid.
  • vendor layer refers to a layer that is in direct contact with the refrigerant fluid.
  • a so-called veneer structure comprises the resin composition described herein as its innermost layer in direct contact with the refrigerant fluid. Fittings may inserted into the end of the hollow structure. If the hollow structure has a hard surface, specially designed fittings often comprising O-rings can be used to provide leak-proof sealing between the surface of the fitting and the resin composition described herein.
  • a so-called barrier structure comprises a resin made of a material other than the resin composition described herein, such as for example an elastomeric material, as its innermost layer, in direct contact with the refrigerant fluid and a barrier layer made of the resin composition described herein located outward of the innermost layer.
  • a resin made of a material other than the resin composition described herein such as for example an elastomeric material, as its innermost layer, in direct contact with the refrigerant fluid and a barrier layer made of the resin composition described herein located outward of the innermost layer.
  • the barrier layer made of the resin composition described herein is sandwiched between at least two other layers of the multilayer structure.
  • multilayer hollow structure examples include without limitation multilayer hollow structures comprising one or more barrier layers made of the resin composition described herein and an innermost layer made of a material other than the resin composition described herein; multilayer hollow structures comprising one or more layers made of the resin composition described herein and an outermost layer made of a material other than the resin composition described herein; multilayer hollow structures comprising one or more layers made of the resin composition described herein, an innermost layer and an outermost layer made of a material other than the resin composition described herein; and multilayer hollow structures comprising one or more layers made of the resin composition described herein and one or more functional layers; and combinations thereof.
  • multilayer hollow structures comprising one or more layers made of the resin composition described herein and an innermost layer made of a material other than the resin composition described herein.
  • the term “innermost layer” refers to a layer that is in direct contact with the refrigerant fluid to be conveyed.
  • the innermost layer comprises an elastomeric material that is able to seal against the surface of a fitting inserted at one of the ends of the structure.
  • the elastomeric material is preferably a non-fluorinated rubber.
  • Preferred non-fluorinated rubbers are selected from acrylonitrile-butadiene rubber (NBR), hydrogenated acrylonitrile-butadiene rubber (HNBR), epichlorohydrin rubber (ECO), chlorosulfonated rubber (CSM), butyl rubber (IIR) and mixtures thereof.
  • the innermost layer can comprise of a thermoplastic material selected from polyamides, polyesters and TEE.
  • multilayer hollow structures comprising one or more layers made of the resin composition described herein and an outermost layer made of a material other than the resin composition described herein.
  • the term outermost layer refers to a layer that faces the environment.
  • the outermost layer may be made of one or more suitable elastomeric or plastic materials designed to withstand the exterior environment encountered.
  • the material for the outermost layer is not specifically limited, but examples thereof include polyamide resins, polyolefin resins and thermoplastic elastomers and rubbers, which may be used either alone or in combination.
  • thermoplastic elastomers and rubbers include without limitation acrylonitrile-butadiene rubber (NBR), hydrogenated acrylonitrile-butadiene rubber (HNBR), butyl rubber (IIR), chlorosulfonated polyethylene (CSM), polychloroprene rubber (CR), epichlorohydrin rubber (ECO), ethylene-vinyl acetate (EVM), ethylene methylacrylate elastomer (EAM), acrylic or acrylate elastomer (ACM), nitrile-polyvinylchloride (NBR-PVC) blended elastomer, chlorinated polyethylene (CPE), ethylene-alpha-olefin elastomer, ethylene-propylene-diene elastomer (EPDM) and mixtures thereof.
  • NBR acrylonitrile-butadiene rubber
  • HNBR hydrogenated acrylonitrile-butadiene rubber
  • IIR butyl rubber
  • the multilayer hollow structures described herein may further comprise one or more functional layers, which functional layers may be situated over the outermost layer or inside the innermost layer of the hollow structure.
  • the one or more functional layers include but are not limited to braidings, reinforcement layers, thermal shields and softer cover layers.
  • braidings may be filament braidings with polyamide, aramid, polyethylene terephthalate (PET) or metallic filaments and woven fabrics of these materials.
  • thermal shields may be metallic foils such as aluminum foils.
  • softer cover layers may be layers made of rubber or of a thermoplastic elastomer.
  • one or more adhesive layers also called tie layers, intervening tie layers or adhesion-promoting layers may be added between the different layers.
  • the multilayer hollow structures described herein can be manufactured by conventional processes like for example extrusion, blow molding, injection molding, and corrugated extrusion.
  • these layers may be manufactured by processes such as coextrusion or coextrusion blowmolding.
  • a second thermoplastic material include materials comprising for example a polyamide, a copolyamide, a polyester, a polyesterether, a functionalized polyolefin or a thermoplastic vulcanizate.
  • a multilayer co-extrusion process separate extruders are used to extrude each type of polymeric compositions.
  • the temperature settings and other processing conditions for the extruders are arranged such that they are appropriate to the composition being extruded. This avoids having to expose lower melting polymeric compositions to higher than normal processing temperatures during the extrusion step while allowing the extrusion of higher melting polymeric compositions at a suitable temperature.
  • the individual melts from the extrusion streams are combined together in a suitably designed die and arranged in the desired multilayer arrangement
  • the multilayer hollow structure comprising at least one layer made of the resin composition described herein and layers made of elastomeric materials can be made by a sequential process wherein each individual layer is extruded in sequence over a pre-extruded underlying layer, braiding layer is constructed at appropriate location, and the complete hollow structure is cured in order to cure the elastomeric layers.
  • one barrier layer, one braiding layer and two elastomeric layers may be constructed as follows: a hollow structure made of the resin composition described herein is first extruded to form the innermost layer and a layer of uncured elastomeric compound is then extruded over the first layer to form a second layer of the hose.
  • the elastomeric compound may be modified to enhance its adhesion to the layer made of the resin composition described herein.
  • the structure may be cooled to a low temperature, and then a braiding layer of filaments may be applied over the elastomeric layer.
  • a second layer of the same or a different uncured elastomeric compound is then extruded over the braiding layer.
  • the entire structure is subjected to a curing process to cure the elastomeric layers and ensure adhesion among the respective layers to form the multilayer hollow structure comprising a layer made of the resin composition described herein.
  • the present invention relates to a method for conveying a refrigerant fluid comprising a step of passing the refrigerant fluid through the hollow structure described herein.
  • the present invention relates a refrigerant device comprising the hollow structure described herein.
  • refrigerant device include without limitation automotive air-conditioning systems, building heating, ventilation and air conditioning systems, refrigerated storage systems, refrigerated transportation systems and such where a refrigerant fluid needs to be conveyed between various components of the device.
  • the following materials were used for preparing the resin composition to be used to make the hollow structure of the present invention and a comparative example.
  • Polyamide PA66/6T copolyamide made from a) group A monomers consisting of terephthalic acid and hexamethylenediamine; and b) group B monomers consisting of adipic acid and hexamethylenediamine, wherein the monomers of group A are present in an amount of 25 mole-percent and the monomers of group B are present in an amount of 75 mole-percent, the weight percentages being based on the copolyamide.
  • Polyamide PA6 Compound a commercially available PA6 described as an extrudable super tough polyamide 6 resin suitable for hose inner cores, such a product is commercially available from E. I. du Pont de Nemours and Company, Wilmington, Del.
  • MAH-g-ethylene octene copolymer ethylene octene copolymer comprising 72 weight percent of ethylene, 28 weight percent of octene and about 0.6 weight percent of grafted maleic anhydride.
  • Ethylene-octene polymer a polymer comprising 72 weight percent of ethylene, 28 weight percent of octene supplied from Dow Chemicals under the name EngageTM.
  • N-butyl benzene sulphonamide plasticizer supplied by Unitex Chemical Corportation, Greensboro, N.C., USA under the name Uniplex 214
  • Antioxidant 1 N,N′-hexane-1,6-diylbis(3-(3,5-di-tert-butyl-4-hydroxyphenylpropionamide)) supplied by Ciba Specialty Chemicals, Tarrytown, N.Y., USA under the tradename Irganox® 1098.
  • Antioxidant 2 tris(2,4-ditert-butylphenyl)phosphite supplied by Ciba Specialty Chemicals, Tarrytown, N.Y., USA under the tradename Irgafox® 168.
  • Heat stabilizer mixture of potassium iodide, copper iodide and aluminum distearate in a 7:1:1 ratio.
  • Refrigerant fluid a mixture comprising 50% of HFO 1234 yf (2,3,3,3-tetrafluoropropene supplied by DuPont, 50% of a proprietary polyalkylene glycol (PAG) based lubricant referred to as ND8S5 supplied by Idemitsu and 2000 ppm H 2 O based on the weight of the oil.
  • PAG polyalkylene glycol
  • the composition of the Example (E1) was prepared by melt blending ingredients shown in Table 1 in a ZSK 25 mm twin screw extruder operating at about 260° C. and a throughput of about 15 kg/h. Ingredient quantities shown in Table 1 are given in weight percent on the basis of the total weight of the resin composition.
  • the compounded mixture was extruded in the form of laces or strands, cooled in a water bath, chopped into granules and placed into sealed aluminum lined bags in order to prevent moisture pick up.
  • the composition of the Comparative Example (C1) was used as commercially available resin form. All materials were dried overnight at 70° C. in a dehumidified drier prior to further use.
  • test pieces Preparation of test pieces.
  • the compositions E1 and C1 were extruded into a thin sheet.
  • E1 composition was extruded into a 0.17 mm thick flat sheet using a sheet casting line with 45 mm (1.75′′) 24:1 L/D Wayne extruder with a 200 mm (8′′) wide coathanger type sheet die at a melt temperature of about 260° C.
  • Dogbone shaped tensile test pieces measuring 63 mm long, 3.2 mm wide in the gauge section and 9.5 mm wide at the ends were die-cut from the sheet.
  • Dogbone shaped tensile test pieces from a 0.15 mm thick sheet of composition C1 were procured for comparative testing. These test pieces measured about 45 mm long, 6 mm wide in the gauge section and 17 mm wide at the ends.
  • Test specimens were dried at 60° C. for 24 hrs in a dehumidified dryer, and individually sealed into glass tubes containing 4 mL of the refrigerant fluid (as described in the “Materials” section).
  • Two tubes were prepared for test pieces of composition E1 and three tubes were prepared for test pieces of composition C1.
  • the tubes were heated in an oven with circulating hot air at a temperature of 150° C. for 300 hours. At the end of the heating, the glass tubes were broken and the test pieces were retrieved for measurements.
  • Tensile properties of the test pieces before and after heat ageing were measured at room temperature on a tensile tester by gripping the wide ends of the dogbone shaped test pieces in the upper and lower grips, and stretching the test pieces at a crosshead speed of 50 mm/min.
  • the average values of tensile strength before and after heat ageing are given in Table 1.
  • Polyamide or copolyamide phase of each composition was thus dissolved and the solution was used to determine the MW.
  • the average values of MW before and after heat ageing are given in Table 1.
  • the retention of tensile strength and MW is reported as the percentage of the tensile strength and MW retained after aging at 150° C. for 300 hours, in comparison with the value of the specimens prior to ageing (i.e. unaged) considered as being 100%. Retention results are given in Table 1.
  • test pieces made of the composition E1 comprising a semi-aromatic copolyamide and a functionalized polyolefin exhibited improved retention of the tensile strength and MW at the end of ageing test compared to comparative test pieces mad of composition C1.

Landscapes

  • Engineering & Computer Science (AREA)
  • Mechanical Engineering (AREA)
  • General Engineering & Computer Science (AREA)
  • Physics & Mathematics (AREA)
  • Thermal Sciences (AREA)
  • Laminated Bodies (AREA)
  • Rigid Pipes And Flexible Pipes (AREA)
  • Compositions Of Macromolecular Compounds (AREA)
US12/963,772 2009-12-16 2010-12-09 Hollow structures and associated method for conveying refrigerant fluids Abandoned US20110155359A1 (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
US12/963,772 US20110155359A1 (en) 2009-12-16 2010-12-09 Hollow structures and associated method for conveying refrigerant fluids

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
US28697709P 2009-12-16 2009-12-16
US12/963,772 US20110155359A1 (en) 2009-12-16 2010-12-09 Hollow structures and associated method for conveying refrigerant fluids

Publications (1)

Publication Number Publication Date
US20110155359A1 true US20110155359A1 (en) 2011-06-30

Family

ID=43663503

Family Applications (1)

Application Number Title Priority Date Filing Date
US12/963,772 Abandoned US20110155359A1 (en) 2009-12-16 2010-12-09 Hollow structures and associated method for conveying refrigerant fluids

Country Status (6)

Country Link
US (1) US20110155359A1 (enExample)
EP (1) EP2512794A1 (enExample)
JP (1) JP2013514442A (enExample)
CN (1) CN102656009A (enExample)
CA (1) CA2781438A1 (enExample)
WO (1) WO2011084421A1 (enExample)

Cited By (10)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
WO2013033190A1 (en) * 2011-08-29 2013-03-07 E. I. Du Pont De Nemours And Company Copolyamide compositions derived from vegetable oil
WO2014125219A1 (fr) 2013-02-18 2014-08-21 Arkema France Structure thermoplastique pour le transport de fluide frigorigene
WO2014125218A1 (fr) 2013-02-18 2014-08-21 Arkema France Utilisation de copolyamide semi-aromatique pour le transport de fluide frigorigène
US20150329670A1 (en) * 2012-11-12 2015-11-19 Mitsui Chemicals, Inc. Semiaromatic polyamide, semiaromatic polyamide resin composition, and molded article
WO2017009131A1 (en) * 2015-07-14 2017-01-19 Wavin B.V. Multilayered pipe and method of manufacturing the same
US10889081B2 (en) 2016-06-01 2021-01-12 Wavin B.V. Multi-layered pipe and a method for forming a multi-layered pipe
US20220099222A1 (en) * 2020-09-30 2022-03-31 Contitech Techno-Chemie Gmbh Vehicle air conditioning hose inner layer
US20220266568A1 (en) * 2017-02-20 2022-08-25 Mitsui Chemicals, Inc. Laminate
US11634564B2 (en) 2021-03-22 2023-04-25 Contitech Transportbandsysteme Gmbh High heat and oil resistant conveyor belt
US11787939B2 (en) 2019-10-24 2023-10-17 Inv Nylon Polymers Americas, Llc Polyamide compositions and articles made therefrom

Families Citing this family (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US20120279605A1 (en) * 2011-05-04 2012-11-08 E.I. Du Pont De Nemours And Company Polyamide compositions for the inner layer of a multi-layer tubular article and articles incorporating same
GB2635825A (en) * 2022-10-24 2025-05-28 Titeflex Corp Multilayer composite pipe and pipe assemblies including reflective insulation

Citations (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US4319872A (en) * 1976-12-01 1982-03-16 Lupke Gerd Paul Heinrich Apparatus for producing thermoplastic tubing
US5846478A (en) * 1991-03-18 1998-12-08 Toray Industries, Inc. Process for producing polyamide blow molded product
US6764627B2 (en) * 2000-03-23 2004-07-20 Hahn Elastomer Corporation Method of making corrugated part
US20090269532A1 (en) * 2008-03-03 2009-10-29 Arkema France Multilayer structure comprising at least one stabilized layer

Family Cites Families (8)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
DE69518357T2 (de) * 1994-05-31 2001-04-05 Ube Industries, Ltd. Polyamid-terpolymer, diese enthaltende Polyamidharzzusammensetzung und daraus hergestellte Automobilteile
US6376036B1 (en) 1998-03-26 2002-04-23 The Goodyear Tire & Rubber Company Air conditioning hose
JP2001049063A (ja) * 1999-08-06 2001-02-20 Tokai Rubber Ind Ltd ゴム組成物、ゴム−樹脂積層体及び不透過性ホース
AU2002359806A1 (en) 2001-12-21 2003-07-15 Rubbermaid Incorporated Apparatus and method for forming discrete hollow parts
KR101094515B1 (ko) * 2003-06-05 2011-12-19 이 아이 듀폰 디 네모아 앤드 캄파니 에틸렌 산 공중합체 및 폴리아미드를 포함하는 내마모성조성물
ES2541450T3 (es) * 2005-03-18 2015-07-20 Kuraray Co., Ltd. Resina de poliamida semiaromática
AR053845A1 (es) * 2005-04-15 2007-05-23 Tibotec Pharm Ltd 5-tiazolilmetil[(1s,2r)-3-[[(2-amino-6-benzoxazolil)sulfonil)](2-metilpropil)amino]-2-hidroxi-1-(fenilmetil)propil]carbamato como mejorador de farmacos metabolizados por el citocromo p450
US20090162591A1 (en) * 2007-06-22 2009-06-25 Shailesh Ratilal Doshi Multilayer coolant pipes

Patent Citations (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US4319872A (en) * 1976-12-01 1982-03-16 Lupke Gerd Paul Heinrich Apparatus for producing thermoplastic tubing
US5846478A (en) * 1991-03-18 1998-12-08 Toray Industries, Inc. Process for producing polyamide blow molded product
US6764627B2 (en) * 2000-03-23 2004-07-20 Hahn Elastomer Corporation Method of making corrugated part
US20090269532A1 (en) * 2008-03-03 2009-10-29 Arkema France Multilayer structure comprising at least one stabilized layer

Cited By (27)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
WO2013033190A1 (en) * 2011-08-29 2013-03-07 E. I. Du Pont De Nemours And Company Copolyamide compositions derived from vegetable oil
US20150329670A1 (en) * 2012-11-12 2015-11-19 Mitsui Chemicals, Inc. Semiaromatic polyamide, semiaromatic polyamide resin composition, and molded article
US9932444B2 (en) * 2012-11-12 2018-04-03 Mitsui Chemicals, Inc. Semiaromatic polyamide, semiaromatic polyamide resin composition, and molded article
US10023695B2 (en) * 2013-02-18 2018-07-17 Arkema France Thermoplastic structure for transporting refrigerant fluid
US10914409B2 (en) 2013-02-18 2021-02-09 Arkema France Use of semi-aromatic copolyamide for transporting refrigerant fluid
FR3002180A1 (fr) * 2013-02-18 2014-08-22 Arkema France Utilisation de copolyamide semi-aromatique pour le transport de fluide frigorigene
US20150376335A1 (en) * 2013-02-18 2015-12-31 Arkema France Thermoplastic structure for transporting refrigerant fluid
US20150377389A1 (en) * 2013-02-18 2015-12-31 Arkema France Use of semi-aromatic copolyamide for transporting refrigerant fluid
JP2016516099A (ja) * 2013-02-18 2016-06-02 アルケマ フランス 冷媒流体を輸送するための半芳香族コポリアミドの使用
US11209105B2 (en) 2013-02-18 2021-12-28 Arkema France Use of semi-aromatic copolyamide for transporting refrigerant fluid
FR3002233A1 (fr) * 2013-02-18 2014-08-22 Arkema France Structure thermoplastique pour le transport de fluide frigorigene
WO2014125218A1 (fr) 2013-02-18 2014-08-21 Arkema France Utilisation de copolyamide semi-aromatique pour le transport de fluide frigorigène
WO2014125219A1 (fr) 2013-02-18 2014-08-21 Arkema France Structure thermoplastique pour le transport de fluide frigorigene
JP2018168374A (ja) * 2013-02-18 2018-11-01 アルケマ フランス 冷媒流体を輸送するための半芳香族コポリアミドの使用
CN109849478A (zh) * 2013-02-18 2019-06-07 阿科玛法国公司 用于传输制冷剂流体的热塑性结构体
US20190178423A1 (en) * 2013-02-18 2019-06-13 Arkema France Use of semi-aromatic copolyamide for transporting refrigerant fluid
US10605385B2 (en) * 2013-02-18 2020-03-31 Arkema France Use of semi-aromatic copolyamide for transporting refrigerant fluid
EA033215B1 (ru) * 2015-07-14 2019-09-30 Вавин Б.В. Многослойная труба и способ ее производства
NL1041400B1 (en) * 2015-07-14 2017-01-30 Wavin Bv Multilayered pipe and method of manufacturing the same.
US11073232B2 (en) 2015-07-14 2021-07-27 Wavin B.V. Multilayered pipe and method of manufacturing the same
WO2017009131A1 (en) * 2015-07-14 2017-01-19 Wavin B.V. Multilayered pipe and method of manufacturing the same
US10889081B2 (en) 2016-06-01 2021-01-12 Wavin B.V. Multi-layered pipe and a method for forming a multi-layered pipe
US20220266568A1 (en) * 2017-02-20 2022-08-25 Mitsui Chemicals, Inc. Laminate
US11787939B2 (en) 2019-10-24 2023-10-17 Inv Nylon Polymers Americas, Llc Polyamide compositions and articles made therefrom
US20220099222A1 (en) * 2020-09-30 2022-03-31 Contitech Techno-Chemie Gmbh Vehicle air conditioning hose inner layer
US11674618B2 (en) * 2020-09-30 2023-06-13 Contitech Techno-Chemie Gmbh Vehicle air conditioning hose inner layer
US11634564B2 (en) 2021-03-22 2023-04-25 Contitech Transportbandsysteme Gmbh High heat and oil resistant conveyor belt

Also Published As

Publication number Publication date
JP2013514442A (ja) 2013-04-25
EP2512794A1 (en) 2012-10-24
CA2781438A1 (en) 2011-07-14
WO2011084421A1 (en) 2011-07-14
CN102656009A (zh) 2012-09-05

Similar Documents

Publication Publication Date Title
US20110155359A1 (en) Hollow structures and associated method for conveying refrigerant fluids
EP2512793B1 (en) Multilayer structures comprising a barrier layer and their use to convey fluids
JP6560620B2 (ja) 冷媒流体を輸送するための半芳香族コポリアミドの使用
CN107250640B (zh) 纤维强化复合管和冷热水配管系统
CN103998525B (zh) 基于半芳族聚酰胺的柔性组合物、其制备方法及其用途
CN107075247B (zh) 包括粘滞性聚酰胺的转变稳定的组合物、其制造及其用途
CN105121549B (zh) 包含半芳族共聚酰胺、聚烯烃和铜热稳定剂的组合物，其制备及其用途
CN103476577A (zh) 包括特定共聚酰胺的层和阻挡层的多层结构体
WO2023282154A1 (ja) ポリアミド組成物
US20090162591A1 (en) Multilayer coolant pipes
CN105985635A (zh) 包含部分芳族聚酰胺层的多层复合件
US20230191756A1 (en) Multilayer structure based on recycled polyamide
KR20170128334A (ko) 연료 수송용 다층 튜브 및 그것을 구비한 연료 펌프 모듈, 그리고 이것들의 사용 방법
WO2012135393A2 (en) Thermoplastic multilayer tubes and process for manufacturing
US11059258B2 (en) Multilayer combining both good ageing properties and resistance to bursting in hot conditions, that can be used for high-temperature motor vehicle applications
JP2019023487A (ja) 冷媒輸送ホース
CN101084117A (zh) 多层聚合物结构

Legal Events

Date Code Title Description
STCB Information on status: application discontinuation

Free format text: ABANDONED -- FAILURE TO RESPOND TO AN OFFICE ACTION