WO2019065834A1 - 発泡樹脂成形品 - Google Patents

発泡樹脂成形品 Download PDF

Info

Publication number
WO2019065834A1
WO2019065834A1 PCT/JP2018/035921 JP2018035921W WO2019065834A1 WO 2019065834 A1 WO2019065834 A1 WO 2019065834A1 JP 2018035921 W JP2018035921 W JP 2018035921W WO 2019065834 A1 WO2019065834 A1 WO 2019065834A1
Authority
WO
WIPO (PCT)
Prior art keywords
resin
mass
foamed resin
resin layer
foamed
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.)
Ceased
Application number
PCT/JP2018/035921
Other languages
English (en)
French (fr)
Inventor
大樹 久宿
保 松永
博章 花木
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.)
Sekisui Chemical Co Ltd
Original Assignee
Sekisui Chemical Co Ltd
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
Family has litigation
First worldwide family litigation filed litigation Critical https://patents.darts-ip.com/?family=65902874&utm_source=google_patent&utm_medium=platform_link&utm_campaign=public_patent_search&patent=WO2019065834(A1) "Global patent litigation dataset” by Darts-ip is licensed under a Creative Commons Attribution 4.0 International License.
Application filed by Sekisui Chemical Co Ltd filed Critical Sekisui Chemical Co Ltd
Priority to KR1020207008352A priority Critical patent/KR102567701B1/ko
Priority to SG11202002766WA priority patent/SG11202002766WA/en
Priority to JP2019524297A priority patent/JP6581749B2/ja
Priority to MYPI2020001617A priority patent/MY200401A/en
Priority to US16/650,164 priority patent/US11530309B2/en
Priority to CN201880062617.2A priority patent/CN111315574B/zh
Priority to PH1/2020/550129A priority patent/PH12020550129B1/en
Publication of WO2019065834A1 publication Critical patent/WO2019065834A1/ja
Anticipated expiration legal-status Critical
Ceased legal-status Critical Current

Links

Images

Classifications

    • C—CHEMISTRY; METALLURGY
    • C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08J—WORKING-UP; GENERAL PROCESSES OF COMPOUNDING; AFTER-TREATMENT NOT COVERED BY SUBCLASSES C08B, C08C, C08F, C08G or C08H
    • C08J9/00—Working-up of macromolecular substances to porous or cellular articles or materials; After-treatment thereof
    • C08J9/34—Chemical features in the manufacture of articles consisting of a foamed macromolecular core and a macromolecular surface layer having a higher density than the core
    • 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
    • B32B25/00—Layered products comprising a layer of natural or synthetic rubber
    • B32B25/04—Layered products comprising a layer of natural or synthetic rubber comprising rubber as the main or only constituent of a layer, which is next to another layer of the same or of a different material
    • B32B25/045—Layered products comprising a layer of natural or synthetic rubber comprising rubber as the main or only constituent of a layer, which is next to another layer of the same or of a different material of foam
    • 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
    • B32B27/065—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 foam
    • 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
    • B32B27/18—Layered products comprising a layer of synthetic resin characterised by the use of special additives
    • 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
    • B32B27/28—Layered products comprising a layer of synthetic resin comprising synthetic resins not wholly covered by any one of the sub-groups B32B27/30 - B32B27/42
    • 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
    • B32B27/28—Layered products comprising a layer of synthetic resin comprising synthetic resins not wholly covered by any one of the sub-groups B32B27/30 - B32B27/42
    • B32B27/281—Layered products comprising a layer of synthetic resin comprising synthetic resins not wholly covered by any one of the sub-groups B32B27/30 - B32B27/42 comprising polyimides
    • 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
    • B32B27/28—Layered products comprising a layer of synthetic resin comprising synthetic resins not wholly covered by any one of the sub-groups B32B27/30 - B32B27/42
    • B32B27/285—Layered products comprising a layer of synthetic resin comprising synthetic resins not wholly covered by any one of the sub-groups B32B27/30 - B32B27/42 comprising polyethers
    • 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
    • B32B27/30—Layered products comprising a layer of synthetic resin comprising vinyl (co)polymers; comprising acrylic (co)polymers
    • 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
    • B32B27/30—Layered products comprising a layer of synthetic resin comprising vinyl (co)polymers; comprising acrylic (co)polymers
    • B32B27/302—Layered products comprising a layer of synthetic resin comprising vinyl (co)polymers; comprising acrylic (co)polymers comprising aromatic vinyl (co)polymers, e.g. styrenic (co)polymers
    • 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
    • B32B27/30—Layered products comprising a layer of synthetic resin comprising vinyl (co)polymers; comprising acrylic (co)polymers
    • B32B27/308—Layered products comprising a layer of synthetic resin comprising vinyl (co)polymers; comprising acrylic (co)polymers comprising acrylic (co)polymers
    • 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
    • B32B27/36—Layered products comprising a layer of synthetic resin comprising polyesters
    • 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
    • B32B3/00—Layered products comprising a layer with external or internal discontinuities or unevennesses, or a layer of non-planar shape; Layered products comprising a layer having particular features of form
    • B32B3/02—Layered products comprising a layer with external or internal discontinuities or unevennesses, or a layer of non-planar shape; Layered products comprising a layer having particular features of form characterised by features of form at particular places, e.g. in edge regions
    • B32B3/04—Layered products comprising a layer with external or internal discontinuities or unevennesses, or a layer of non-planar shape; Layered products comprising a layer having particular features of form characterised by features of form at particular places, e.g. in edge regions characterised by at least one layer folded at the edge, e.g. over another layer ; characterised by at least one layer enveloping or enclosing a material
    • 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
    • B32B5/00—Layered products characterised by the non- homogeneity or physical structure, i.e. comprising a fibrous, filamentary, particulate or foam layer; Layered products characterised by having a layer differing constitutionally or physically in different parts
    • B32B5/18—Layered products characterised by the non- homogeneity or physical structure, i.e. comprising a fibrous, filamentary, particulate or foam layer; Layered products characterised by having a layer differing constitutionally or physically in different parts characterised by features of a layer of foamed material
    • 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
    • B32B7/00—Layered products characterised by the relation between layers; Layered products characterised by the relative orientation of features between layers, or by the relative values of a measurable parameter between layers, i.e. products comprising layers having different physical, chemical or physicochemical properties; Layered products characterised by the interconnection of layers
    • B32B7/02—Physical, chemical or physicochemical properties
    • B32B7/022—Mechanical properties
    • C—CHEMISTRY; METALLURGY
    • C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08L—COMPOSITIONS OF MACROMOLECULAR COMPOUNDS
    • C08L9/00—Compositions of homopolymers or copolymers of conjugated diene hydrocarbons
    • 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
    • F16L59/00—Thermal insulation in general
    • F16L59/14—Arrangements for the insulation of pipes or pipe systems
    • F16L59/143—Pre-insulated pipes
    • 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
    • F16L59/00—Thermal insulation in general
    • F16L59/14—Arrangements for the insulation of pipes or pipe systems
    • F16L59/16—Arrangements specially adapted to local requirements at flanges, junctions, valves or the like
    • F16L59/163—Branch units; Insulation forming a whole with branches
    • 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
    • F16L59/00—Thermal insulation in general
    • F16L59/14—Arrangements for the insulation of pipes or pipe systems
    • F16L59/16—Arrangements specially adapted to local requirements at flanges, junctions, valves or the like
    • F16L59/22—Arrangements specially adapted to local requirements at flanges, junctions, valves or the like adapted for bends
    • 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
    • B32B2250/00—Layers arrangement
    • B32B2250/02—2 layers
    • 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
    • B32B2250/00—Layers arrangement
    • B32B2250/24—All layers being polymeric
    • 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
    • B32B2250/00—Layers arrangement
    • B32B2250/44—Number of layers variable across the laminate
    • 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
    • B32B2266/00—Composition of foam
    • B32B2266/02—Organic
    • B32B2266/0207—Materials belonging to B32B25/00
    • 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
    • B32B2266/00—Composition of foam
    • B32B2266/02—Organic
    • B32B2266/0214—Materials belonging to B32B27/00
    • 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
    • B32B2266/00—Composition of foam
    • B32B2266/02—Organic
    • B32B2266/0214—Materials belonging to B32B27/00
    • B32B2266/0221—Vinyl resin
    • B32B2266/0228—Aromatic vinyl resin, e.g. styrenic (co)polymers
    • 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
    • B32B2266/00—Composition of foam
    • B32B2266/02—Organic
    • B32B2266/0214—Materials belonging to B32B27/00
    • B32B2266/0242—Acrylic 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
    • B32B2270/00—Resin or rubber layer containing a blend of at least two different polymers
    • 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
    • B32B2307/00—Properties of the layers or laminate
    • B32B2307/30—Properties of the layers or laminate having particular thermal properties
    • B32B2307/304—Insulating
    • 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
    • B32B2307/00—Properties of the layers or laminate
    • B32B2307/40—Properties of the layers or laminate having particular optical properties
    • B32B2307/412—Transparent
    • 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
    • B32B2307/00—Properties of the layers or laminate
    • B32B2307/70—Other properties
    • B32B2307/714—Inert, i.e. inert to chemical degradation, corrosion
    • 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
    • B32B2355/00—Specific polymers obtained by polymerisation reactions only involving carbon-to-carbon unsaturated bonds, not provided for in a single one of index codes B32B2323/00 - B32B2333/00
    • B32B2355/02—ABS polymers, i.e. acrylonitrile-butadiene-styrene polymers
    • 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
    • B32B2597/00—Tubular articles, e.g. hoses, pipes
    • C—CHEMISTRY; METALLURGY
    • C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08J—WORKING-UP; GENERAL PROCESSES OF COMPOUNDING; AFTER-TREATMENT NOT COVERED BY SUBCLASSES C08B, C08C, C08F, C08G or C08H
    • C08J2203/00—Foams characterized by the expanding agent
    • C08J2203/04—N2 releasing, ex azodicarbonamide or nitroso compound
    • C—CHEMISTRY; METALLURGY
    • C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08J—WORKING-UP; GENERAL PROCESSES OF COMPOUNDING; AFTER-TREATMENT NOT COVERED BY SUBCLASSES C08B, C08C, C08F, C08G or C08H
    • C08J2309/00—Characterised by the use of homopolymers or copolymers of conjugated diene hydrocarbons
    • C08J2309/06—Copolymers with styrene
    • C—CHEMISTRY; METALLURGY
    • C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08J—WORKING-UP; GENERAL PROCESSES OF COMPOUNDING; AFTER-TREATMENT NOT COVERED BY SUBCLASSES C08B, C08C, C08F, C08G or C08H
    • C08J2333/00—Characterised by the use of homopolymers or copolymers of compounds having one or more unsaturated aliphatic radicals, each having only one carbon-to-carbon double bond, and only one being terminated by only one carboxyl radical, or of salts, anhydrides, esters, amides, imides, or nitriles thereof; Derivatives of such polymers
    • C08J2333/04—Characterised by the use of homopolymers or copolymers of compounds having one or more unsaturated aliphatic radicals, each having only one carbon-to-carbon double bond, and only one being terminated by only one carboxyl radical, or of salts, anhydrides, esters, amides, imides, or nitriles thereof; Derivatives of such polymers esters
    • C08J2333/06—Characterised by the use of homopolymers or copolymers of compounds having one or more unsaturated aliphatic radicals, each having only one carbon-to-carbon double bond, and only one being terminated by only one carboxyl radical, or of salts, anhydrides, esters, amides, imides, or nitriles thereof; Derivatives of such polymers esters of esters containing only carbon, hydrogen, and oxygen, the oxygen atom being present only as part of the carboxyl radical
    • C08J2333/10—Homopolymers or copolymers of methacrylic acid esters
    • C08J2333/12—Homopolymers or copolymers of methyl methacrylate
    • C—CHEMISTRY; METALLURGY
    • C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08J—WORKING-UP; GENERAL PROCESSES OF COMPOUNDING; AFTER-TREATMENT NOT COVERED BY SUBCLASSES C08B, C08C, C08F, C08G or C08H
    • C08J2409/00—Characterised by the use of homopolymers or copolymers of conjugated diene hydrocarbons
    • C08J2409/06—Copolymers with styrene
    • C—CHEMISTRY; METALLURGY
    • C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08J—WORKING-UP; GENERAL PROCESSES OF COMPOUNDING; AFTER-TREATMENT NOT COVERED BY SUBCLASSES C08B, C08C, C08F, C08G or C08H
    • C08J2433/00—Characterised by the use of homopolymers or copolymers of compounds having one or more unsaturated aliphatic radicals, each having only one carbon-to-carbon double bond, and only one being terminated by only one carboxyl radical, or of salts, anhydrides, esters, amides, imides, or nitriles thereof; Derivatives of such polymers
    • C08J2433/04—Characterised by the use of homopolymers or copolymers of compounds having one or more unsaturated aliphatic radicals, each having only one carbon-to-carbon double bond, and only one being terminated by only one carboxyl radical, or of salts, anhydrides, esters, amides, imides, or nitriles thereof; Derivatives of such polymers esters
    • C08J2433/06—Characterised by the use of homopolymers or copolymers of compounds having one or more unsaturated aliphatic radicals, each having only one carbon-to-carbon double bond, and only one being terminated by only one carboxyl radical, or of salts, anhydrides, esters, amides, imides, or nitriles thereof; Derivatives of such polymers esters of esters containing only carbon, hydrogen, and oxygen, the oxygen atom being present only as part of the carboxyl radical
    • C08J2433/10—Homopolymers or copolymers of methacrylic acid esters
    • C08J2433/12—Homopolymers or copolymers of methyl methacrylate
    • C—CHEMISTRY; METALLURGY
    • C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08J—WORKING-UP; GENERAL PROCESSES OF COMPOUNDING; AFTER-TREATMENT NOT COVERED BY SUBCLASSES C08B, C08C, C08F, C08G or C08H
    • C08J9/00—Working-up of macromolecular substances to porous or cellular articles or materials; After-treatment thereof
    • C08J9/04—Working-up of macromolecular substances to porous or cellular articles or materials; After-treatment thereof using blowing gases generated by a previously added blowing agent
    • C08J9/06—Working-up of macromolecular substances to porous or cellular articles or materials; After-treatment thereof using blowing gases generated by a previously added blowing agent by a chemical blowing agent
    • C08J9/10—Working-up of macromolecular substances to porous or cellular articles or materials; After-treatment thereof using blowing gases generated by a previously added blowing agent by a chemical blowing agent developing nitrogen, the blowing agent being a compound containing a nitrogen-to-nitrogen bond
    • C08J9/102—Azo-compounds
    • C08J9/103—Azodicarbonamide
    • G—PHYSICS
    • G01—MEASURING; TESTING
    • G01N—INVESTIGATING OR ANALYSING MATERIALS BY DETERMINING THEIR CHEMICAL OR PHYSICAL PROPERTIES
    • G01N3/00—Investigating strength properties of solid materials by application of mechanical stress
    • G01N3/32—Investigating strength properties of solid materials by application of mechanical stress by applying repeated or pulsating forces

Definitions

  • the present invention relates to a foamed resin molded article used for connection of a drain pipe or the like.
  • Priority is claimed on Japanese Patent Application No. 2017-189562, filed on Sep. 29, 2017, the content of which is incorporated herein by reference.
  • Patent Document 1 has a heat insulating layer made of foamed resin in the inside of the main body, and a pipe with a heat insulating layer in which the inner and outer walls of the main body surrounding the heat insulating layer and the connection are integrally formed by injection molding. Fittings have been proposed.
  • Polyvinyl chloride, an acrylonitrile-butadiene-styrene copolymer (ABS resin), polyethylene, a polypropylene etc. are mentioned as resin which can be used for the pipe joint of patent document 1, In an existing product, impact resistance and heat resistance are mentioned. ABS resin is used.
  • ABS resin is excellent in impact resistance and heat resistance as initial performance, but is inferior in chemical resistance. Therefore, in the case of the ABS resin joint, when the organic solvent or the oil is present in the drain pipe, the inner and outer walls of the main body portion may be deteriorated and the heat insulating property may be deteriorated. Then, this invention aims at the foamed resin molded article which is excellent in heat insulation and chemical resistance.
  • the present inventors have found that chemical resistance can be improved by reducing the content of a rubber component such as butadiene contained in the ABS resin and the like constituting the foamed resin molded article.
  • a rubber component such as butadiene contained in the ABS resin and the like constituting the foamed resin molded article.
  • the foamed resin molded product can be made transparent, and the connection portion between the pipe and the pipe joint can be easily recognized visually.
  • a foamed resin layer comprising a first resin which is a copolymer comprising a rubber component, a vinyl cyanide monomer unit and an aromatic vinyl monomer unit, and a foaming agent, and the foamed resin layer And a non-foamed resin layer covering the
  • the non-foamed resin layer contains a second resin which is a copolymer containing a rubber component, a vinyl cyanide-based monomer unit and an aromatic vinyl-based monomer unit,
  • the content of the rubber component of the non-foamed resin layer determined by pyrolysis gas chromatography-mass spectrometry (PGC / MS) is 1% by mass or more and 30% by mass or less based on the total mass of the second resin Is a foamed resin molded article.
  • PLC / MS pyrolysis gas chromatography-mass spectrometry
  • the foamed resin molded article of the present invention is excellent in heat insulation and chemical resistance.
  • FIG. 1 It is a side view showing a foaming resin-molding article concerning one embodiment of the present invention. It is a longitudinal cross-sectional view of the foamed resin molded product shown in FIG. It is a fragmentary sectional view showing a foaming resin-molding article concerning other embodiments of the present invention. It is a side view which shows the piping structure of a stretching fatigue test.
  • the foamed resin molded article 1 is an example of a joint (L-shaped pipe joint joint generally referred to as “elbow”) used for connecting a drain pipe.
  • the foamed resin molded article 1 has a flow path which is bent inside, and is provided with a main body portion 10 having an opening 12a and an opening 12b at both ends.
  • the foamed resin molded product 1 includes a cylindrical receiving portion 20 a surrounding the periphery of the opening 12 a of the main body 10 and a cylindrical receiving portion 20 b surrounding the periphery of the opening 12 b of the main body 10.
  • the main body 10, the receptacle 20a, and the receptacle 20b are integrally formed.
  • FIG. 2 is a longitudinal sectional view of the foamed resin molded article 1 shown in FIG.
  • the main body portion 10 includes a foamed resin layer 30 and a non-foamed resin layer 50. Both surfaces of the foamed resin layer 30 are covered with the non-foamed resin layer 50.
  • the receptacle 20 a and the receptacle 20 b are formed of the non-foamed resin layer 50.
  • a part of the foamed resin layer 30 bites into the non-foamed resin layer 50 of the receiving portion 20 a.
  • a part of the foamed resin layer 30 bites into the non-foamed resin layer 50 of the receiving portion 20 b.
  • a stopper 13 a is formed on the periphery of the opening 12 a of the main body 10.
  • the length from the receptacle end 22a of the receptacle 20a to the stopper 13a is L1.
  • the thickness in the vicinity of the stopper 13a of the receiving portion 20a is d1.
  • the structure of the receptacle 20b is the same as the structure of the receptacle 20a.
  • the foamed resin molded article according to the embodiment of the present invention may be a joint (a three-way branched T-shaped pipe joint joint generally referred to as "tees").
  • the foamed resin molded article 2 has a first tube axis O1 and a second tube axis O2.
  • the two tube axes O1 and O2 are straight and intersect each other at an angle of 90.0 ° to 91.1 °.
  • the foamed resin molded product 2 has a tubular main body portion 210 having a flow path (for example, a drain flow path) inside, and three socket portions 220a, 220b and 220c integrally formed in the opening of the main body portion 210.
  • the inner diameters of the three inlets 220a, 220b and 220c are larger than the inner diameter of the main body 210 in order to insert and connect the tubular member with the foam layer.
  • the foamed resin molded product 2 has socket portions 220a and 220b at three openings of both ends 212a and 212b of the main body portion 210 forming a straight pipe and a branched end 212c opening in the second pipe axis O2 direction.
  • a cheese member 220c is provided in the main body portion 210.
  • an injection gate portion 214 which is a position to be injected at the time of molding is provided at a position opposite to the branch end portion 212c with the first tube axis O1 interposed therebetween.
  • a stopper 213 a is formed on the peripheral edge of the opening end 212 a of the main body 210 and is connected to the inner circumferential surface of the main body 210.
  • a stopper 213 c is formed on the periphery of the branched end portion 212 c of the main body portion 210.
  • the main body portion 210 includes a foamed resin layer 230 and a non-foamed resin layer 250. Both surfaces of the foamed resin layer 230 are covered with the non-foamed resin layer 250.
  • the receptacle 220 a, the receptacle 220 b and the receptacle 220 c are formed of the non-foamed resin layer 250.
  • the length from the socket end 222a of the socket 220a to the open end 212a of the main body 210 is L2.
  • the length L2 is equal to the length from the receiving end 222a to the stopper 213a.
  • the thickness in the vicinity of the stopper 213a of the socket 220a is d2.
  • the structure of the receptacle 220b is the same as the structure of the receptacle 220a. That is, the length from the receiving end 222b to the opening end 212b is L2.
  • the length from the receiving end 222c of the receiving portion 220c to the branched end 212c of the main body 210 is L3.
  • the length L3 is equal to the length from the receiving end 222c to the stopper 213c.
  • the thickness in the vicinity of the stopper 213c of the socket 220c is d3.
  • the foamed resin layer 30 is formed by foaming and molding a foamable resin composition.
  • the foamed resin molded article 1 of the present invention is excellent in heat insulation by having the foamed resin layer 30.
  • the expansion ratio of the foamed resin layer 30 is preferably 1.0 times or more and 8.0 times or less, more preferably 1.1 times or more and 5.0 times or less, and still more preferably 1.2 times or more and 3.0 times or less. By setting the expansion ratio within the above numerical range, high thermal insulation performance can be imparted.
  • the expansion ratio can be adjusted by the type or amount of the resin, the type or amount of the foaming agent, the production conditions and the like. The expansion ratio can be measured by the following method.
  • m ⁇ c / ⁇ (1)
  • m is a foaming ratio
  • ⁇ is an apparent density (g / cm 3 ) of the foamed resin layer
  • ⁇ c is a density (g / cm 3 ) of the foamed resin layer when unfoamed .
  • the density at the time of non-foaming of a foamed resin layer can be measured from what fuse
  • a plurality of cells are formed, substantially no holes are present in the cell walls, and at least some of the plurality of cells are closed cells not in communication with one another. . 85% or more is preferable and 90% or more of a closed cell rate is more preferable.
  • the upper limit is not particularly limited, but is substantially 99% or less. If it is in the said numerical range, low thermal conductivity can be maintained over a long period of time, and it is excellent by heat insulation.
  • the closed cell rate is measured in accordance with JIS K 7138: 2006.
  • the foamable resin composition of the present embodiment contains a first resin, which is a copolymer containing a rubber component, a vinyl cyanide-based monomer unit and an aromatic vinyl-based monomer unit, and a blowing agent.
  • a first resin which is a copolymer containing a rubber component, a vinyl cyanide-based monomer unit and an aromatic vinyl-based monomer unit, and a blowing agent.
  • unit refers to a structural part derived from a monomer compound (monomer) before polymerization
  • cyanide vinyl cyanide monomer unit refers to “cyanide vinyl monomer ( "A structural part derived from acrylonitrile)”.
  • the content ratio of each monomer unit in the polymer corresponds to the content ratio of the monomer in the monomer mixture used for the production of the polymer.
  • (meth) acryl refers to one or both of "acryl” and “methacryl”
  • acrylonitrile refers to one or both of "acrylonitrile” and “
  • the first resin is a copolymer containing a rubber component, a vinyl cyanide monomer unit and an aromatic vinyl monomer unit.
  • a copolymer containing a rubber component, a vinyl cyanide monomer unit and an aromatic vinyl monomer unit is, in the presence of the rubber component, an aromatic vinyl monomer and a vinyl cyanide monomer.
  • a resin obtained by polymerizing the rubber component refers to a raw material of a diene rubber such as polybutadiene and polyisoprene and a monomer component to be a raw material of acrylic rubber.
  • a rubber component in the case of a diene rubber, monomers of a diene rubber such as butadiene, isoprene, ethylene and propylene or polymers thereof are mentioned, and in the case of an acrylic rubber, ethyl acrylate, butyl acrylate, butoxyethyl acrylate And acrylic acid ester monomers such as methoxyethyl acrylate or polymers thereof.
  • Acrylonitrile, methacrylonitrile, etc. are mentioned as a vinyl cyanide type monomer, An acrylonitrile is preferable.
  • the aromatic vinyl monomer examples include styrene, ⁇ -methylstyrene, ⁇ -methylstyrene, 4-methylstyrene, ⁇ -bromostyrene and the like, with styrene and ⁇ -methylstyrene being preferred.
  • Specific examples of the first resin include acrylonitrile-butadiene-styrene copolymer (ABS resin), acrylonitrile-ethylenepropylenediene-styrene copolymer (AES resin), acrylonitrile-acrylic rubber-styrene copolymer (AAS resin) And the like, and they may be further mixed.
  • the content of the rubber component of the first resin is not particularly limited, and is preferably 1% by mass to 30% by mass with respect to the total mass of the first resin.
  • the content of the vinyl cyanide monomer unit in the first resin is preferably 10% by mass to 50% by mass, and more preferably 15% by mass to 45% by mass, based on the total mass of the first resin. preferable.
  • Tensile strength can be improved as content of a vinyl cyanide type monomer unit is more than the above-mentioned lower limit.
  • Impact strength can be improved as content of a vinyl cyanide type monomer unit is below the said upper limit.
  • the content of the aromatic vinyl monomer unit in the first resin is preferably 15% by mass to 60% by mass, and more preferably 20% by mass to 50% by mass, based on the total mass of the first resin. preferable.
  • the content of the aromatic vinyl-based monomer unit is equal to or more than the above lower limit value, the indentation hardness can be improved. Impact strength can be improved as content of an aromatic vinyl-type monomer unit is below the said upper limit.
  • the first resin may contain any monomer unit other than vinyl cyanide monomer unit and aromatic vinyl monomer unit, and examples thereof include polycarbonate resin and its monomer Be
  • the content of each component in the first resin is determined by analysis using pyrolysis gas chromatography-mass spectrometry (PGC / MS).
  • PGC / MS pyrolysis gas chromatography-mass spectrometry
  • An example of measurement conditions using PGC / MS is shown below.
  • Gas chromatograph GC 2010 (Shimadzu Corporation).
  • Mass spectrometer GCMS-QP 2010 (Shimadzu Corporation).
  • Thermal decomposition conditions Thermal decomposition temperature: 550 ° C. Interface temperature: 250 ° C. Gas chromatograph conditions. Carrier flow rate: 1 ml / min (He). Split ratio: 100: 1.
  • each component constituting the first resin is thermally decomposed and separated by pyrolysis gas chromatography to obtain a thermal decomposition pattern (pyrogram) in which each component is recorded as a peak.
  • pyrogram thermal decomposition pattern
  • each component of acrylonitrile, a rubber component, and styrene is specified by a mass spectrum obtained by a mass spectrometer.
  • each component of acrylonitrile, a rubber component, and styrene differs in the degree of depolymerization by pyrolysis (the rate at which the polymer decomposes into a monomer)
  • the area (X) of each peak in the pyrogram is determined by pyrolysis. What was divided by the depolymerization rate (Y) of each component is made into the peak area (Z) of each component.
  • the depolymerization ratio (Y) of each component is acrylonitrile: 0.15, rubber component: 0.10, styrene: 1.0.
  • an acrylic resin such as polymethyl methacrylate
  • the depolymerization ratio of the acrylic resin is 1.0.
  • ratio (Z / T) with respect to the sum total (T) of the peak area (Z) of each component of a thermal decomposition pattern be content (mass%) of each component in 1st resin.
  • Table 1 shows an example of the content of each component obtained by PGC / MS measurement of an acrylonitrile-butadiene-styrene copolymer (ABS resin) containing an acrylic resin.
  • retention time means the time when each component is thermally decomposed to appear as a pyrogram peak.
  • sample amount is the mass of ABS resin subjected to analysis.
  • the content of the first resin with respect to the total mass of the foamable resin composition is preferably 45% by mass to 90% by mass, and more preferably 50% by mass to 85% by mass.
  • the foamable resin composition of the present embodiment may contain another resin other than the first resin.
  • Other resins include, for example, acrylic resins such as methyl polyacrylate, ethyl polyacrylate, glycidyl polyacrylate, polymethyl methacrylate, polyethyl methacrylate, polyglycidyl methacrylate, polyvinyl resin, polyester resin, polyether Resin, polyimide resin, etc. are mentioned. These may be used alone or in combination of two or more.
  • the content of the first resin is preferably 70% by mass or more and 100% by mass or less, and 85% by mass or more and 100% by mass or less based on the total mass of the resin in the foamable resin composition. Is more preferred.
  • any of a volatile foaming agent and a decomposition type foaming agent may be used.
  • volatile blowing agents include aliphatic hydrocarbons, alicyclic hydrocarbons, halogenated hydrocarbons, ethers, ketones and the like.
  • examples of aliphatic hydrocarbons include propane, butane (normal butane, isobutane), pentane (normal pentane, isopentane and the like), and examples of alicyclic hydrocarbons include cyclopentane, cyclohexane and the like. It can be mentioned.
  • halogenated hydrocarbon 1 type (s) or 2 or more types, such as halogenated hydrocarbons, such as trichlorofluoromethane, trichlorotrifluoroethane, tetrafluoroethane, chlorodifluoroethane, difluoroethane etc. are mentioned, for example.
  • halogenated hydrocarbons such as trichlorofluoromethane, trichlorotrifluoroethane, tetrafluoroethane, chlorodifluoroethane, difluoroethane etc.
  • examples of the ether include dimethyl ether and diethyl ether
  • examples of the ketone include acetone and methyl ethyl ketone.
  • degradable foaming agents examples include sodium bicarbonate (sodium bicarbonate), sodium carbonate, ammonium bicarbonate, ammonium nitrite, azide compounds, inorganic foaming agents such as sodium borohydride, azodicarbonamide, barium azodicarboxylate, Organic blowing agents such as dinitrosopentamethylenetetramine can be mentioned.
  • gases such as carbon dioxide gas, nitrogen and air may be used as the foaming agent.
  • decomposable foaming agents are preferable, and among these, sodium bicarbonate and azodicarbonamide are more preferable. These may be used alone or in combination of two or more.
  • the content of the foaming agent is preferably 0.1 to 8 parts by mass, more preferably 1 to 5 parts by mass, and more preferably 1 to 3 parts by mass with respect to 100 parts by mass of the first resin. The following are more preferable.
  • the foamable resin composition of the present invention may contain other components (optional components) other than the first resin, the blowing agent, and the like, as long as the effects of the present invention are not impaired.
  • 50 mass parts or less are preferable with respect to 100 mass parts of 1st resin, as for content of an arbitrary component, 30 mass parts or less are more preferable, and 20 mass parts or less are more preferable.
  • the foamable resin composition of the present invention can contain a first resin, a foaming agent, and optional components.
  • the foamable resin composition may be a mixture in which all the components are previously mixed, or may be in the form of mixing a part or all of all the components in a molding machine.
  • the mixture in which all the components are premixed may be in the form of powder or in the form of pellets.
  • the non-foamed resin layer of this embodiment is formed by molding a non-foamable resin composition.
  • the foamed resin molded article of the present invention can increase the strength of the foamed resin molded article by having the non-foamed resin layer.
  • the non-foamed resin layer covers the foamed resin layer.
  • the non-foamable resin composition of the present embodiment contains a second resin which is a copolymer containing a rubber component, a vinyl cyanide monomer unit and an aromatic vinyl monomer unit.
  • the second resin is a copolymer containing a rubber component, a vinyl cyanide-based monomer unit and an aromatic vinyl-based monomer unit.
  • the second resin may be the same as or different from the first resin.
  • the content of the rubber component in the second resin is 1% by mass or more and 30% by mass or less based on the total mass of the second resin, preferably 1% by mass or more and 25% by mass or less, and 3% by mass or more and 20%. Mass% or less is more preferable, 5 mass% or more and 15 mass% or less is more preferable, and 5 mass% or more and 10 mass% or less is particularly preferable.
  • strength of a foamed resin molded product is easy to be improved as content of a rubber component is more than the said lower limit. When the content of the rubber component is less than or equal to the above upper limit, chemical resistance can be more easily improved.
  • the content of the vinyl cyanide monomer unit in the second resin is preferably 10% by mass to 50% by mass, and more preferably 15% by mass to 45% by mass, based on the total mass of the second resin. preferable.
  • Tensile strength can be improved as content of a vinyl cyanide type monomer unit is more than the above-mentioned lower limit.
  • Impact strength can be improved as content of a vinyl cyanide type monomer unit is below the said upper limit.
  • the content of the aromatic vinyl monomer unit in the second resin is preferably 15% by mass to 60% by mass, and more preferably 20% by mass to 50% by mass, based on the total mass of the second resin. preferable.
  • the content of the aromatic vinyl-based monomer unit is equal to or more than the above lower limit value, the indentation hardness can be improved.
  • Impact strength can be improved as content of an aromatic vinyl-type monomer unit is below the said upper limit.
  • the content of each component in the second resin is determined by analysis using pyrolysis gas chromatography-mass spectrometry (PGC / MS).
  • PPC / MS pyrolysis gas chromatography-mass spectrometry
  • the non-foamable resin composition of the present embodiment may contain another resin other than the second resin.
  • a polyvinyl resin, a polyester resin, a polyether resin, an acrylic resin, a polyimide resin etc. are mentioned, for example. These may be used alone or in combination of two or more.
  • the non-foamable resin composition of the present embodiment preferably further contains an acrylic resin.
  • an acrylic resin the polymer of acrylic acid ester and the polymer of methacrylic acid ester are mentioned, for example.
  • polymers of acrylic esters include methyl polyacrylate, ethyl polyacrylate and glycidyl polyacrylate.
  • polymers of methacrylic acid esters include polymethyl methacrylate, polyethyl methacrylate, and glycidyl polymethacrylate. 20 mass% or more and 60 mass% or less are preferable with respect to the total mass of resin in a non-foaming resin composition, and, as for content of an acrylic resin, 30 mass% or more and 50 mass% or less are more preferable.
  • the strength and the transparency of the foamed resin molded product can be easily enhanced. 10 mass% or more and 55 mass% or less are preferable with respect to the gross mass of non-foaming resin composition, and, as for content of an acrylic resin, 20 mass% or more and 50 mass% or less are more preferable.
  • the content of each component in the non-foaming resin composition containing the second resin and the other resin is determined by analysis using pyrolysis gas chromatography mass spectrometry (PGC / MS).
  • the measurement conditions can be measured under the same conditions as the first resin.
  • the content of each component in the second resin can be calculated by the same calculation method as the content of each component in the first resin.
  • the depolymerization ratio of acrylonitrile, rubber component, styrene, and acrylic resin is acrylonitrile: 0.15, rubber component: 0.10, styrene: 1.0, and acrylic resin: 1.0.
  • the content of the second resin is preferably 40% by mass or more and 100% by mass or less, and 45% by mass or more and 100% by mass with respect to the total mass of the resin in the non-foamable resin composition. % Or less is more preferable, and 50% by mass or more and 100% by mass or less is more preferable.
  • the non-foamable resin composition of the present embodiment may contain other components (optional components) other than the second resin as long as the effects of the present invention are not impaired.
  • other components such as colorants, flame retardants, antioxidants, ultraviolet light absorbers, light stabilizers and the like can be mentioned.
  • the non-foamed resin layer does not have to contain the foaming agent, but may contain the foaming agent.
  • the amount of the foaming agent contained in the non-foamed resin layer is preferably 0 parts by mass or more and 8 parts by mass or less, more preferably 0 parts by mass or more and 5 parts by mass or less, with respect to 100 parts by mass of the second resin More preferably, it is 3 parts by mass or less.
  • the expansion ratio in the non-foamed resin layer is preferably 0, those having a low expansion of 1.5 times or less are not excluded from the present invention.
  • the non-foamable resin composition of the present embodiment can include a second resin and an optional component.
  • the non-foamable resin composition may be a mixture in which all the components are previously mixed, or may be in the form of mixing a part or all of all the components in a molding machine.
  • the mixture in which all the components are premixed may be in the form of powder or in the form of pellets.
  • the non-foamable resin composition of the present embodiment forms a non-foamed resin layer and covers the outer surface of the foamed resin molded article of the present invention.
  • the content of the rubber component in the second resin is 1% by mass or more and 30% by mass or less with respect to the total mass of the second resin. Therefore, the non-foamed resin layer is excellent in chemical resistance, and the foamed resin molded article of the present invention is excellent in chemical resistance.
  • the foamed resin molded article is manufactured by injection molding or extrusion molding.
  • a foamable resin composition having a predetermined expansion ratio can be obtained by heating and melting a foamable resin composition, injecting into a mold, heating at any temperature for any time, and cooling at any temperature for any time. Goods are obtained.
  • the foamable resin composition is heated and melted, poured from the extruder into a mold, and heated at an arbitrary temperature for an arbitrary time to foam and form the foamable resin composition. After cooling at an arbitrary temperature for an arbitrary time, by cutting into a predetermined length, a foamed resin molded article having a predetermined expansion ratio can be obtained.
  • the temperature (molding temperature) of the foamable resin composition immediately before injection into the mold is preferably 200 ° C. or more and 280 ° C. or less, and more preferably 220 ° C. or more and 260 ° C. or less.
  • the time for molding with a mold is preferably 1 minute or more and 10 minutes or less. If it is more than the said lower limit, it can fully be hardened, and if it is below the said upper limit, it will be easy to improve the productivity of a foamed resin molded product.
  • the foamed resin molded product of this invention was demonstrated in detail, this invention is not limited to said one Embodiment, It can change suitably in the range which does not deviate from the meaning.
  • the foamed resin molded product may have only the foamed resin layer without having the non-foamed resin layer.
  • the content of the rubber component may be 1% by mass or more and 30% by mass or less with respect to the total mass of the first resin.
  • the outer surface of the foamed resin layer may form a high density layer as in the non-foamed resin layer.
  • the foamed resin molded article of the present invention may be formed of a foamed resin layer, and may be a multilayer molded article having another different resin layer.
  • resin layers in addition to the non-foamed resin layer, the same foamed resin layer as the outer surface, and a foamed resin layer different from the outer surface may be mentioned.
  • the resin used as the raw material of these resin layers may be the same thermoplastic resin as the foamed resin layer forming the outer surface, or may be a different thermoplastic resin. From the viewpoint of suppressing the peeling between the resin layers, the resin as a raw material of these resin layers is preferably the same thermoplastic resin as the foamed resin layer forming the outer surface.
  • the foamed resin molded product is a foamed pipe joint (elbow) shown in FIG. 2, the length L1 from the receiving end 22a of the receiving portion 20a to the stopper 13a and the thickness in the vicinity of the stopper 13a of the receiving portion 20a 3.5 or more and 10 or less are preferable, as for ratio (henceforth "L1 / d1 ratio") with the length d1, 4.0 or more and 9.0 or less are more preferable, and 4.5 or more and 8.0 or less More preferable.
  • L1 / d1 ratio is equal to or more than the above lower limit, penetration of the foamed resin layer 30 into the socket 20 a is easily suppressed, and a reduction in strength of the socket 20 a is easily suppressed.
  • the foam pipe joint is less likely to be broken due to expansion and contraction fatigue caused by expansion and contraction.
  • the length L1 of the port 20a is sufficiently long that the L1 / d1 ratio is equal to or more than the above lower limit, it is easy to suppress water leakage due to insufficient insertion of piping or the like inserted into the foam pipe joint.
  • the thickness d1 is sufficiently large, and the foam pipe joint is less likely to be broken due to expansion and contraction fatigue caused by expansion and contraction.
  • L1 / d1 ratio is equal to or less than the above upper limit, the length L1 is not too long, and it is easy to suppress concentration of stress due to expansion and contraction at the root of the receiving portion 20a, and the foam pipe joint is expanded and contracted It becomes difficult to be destroyed by the expansion fatigue by.
  • L1 / d1 ratio is the same also in the receptacle 20b of the foamed resin molded product 1.
  • the foamed resin molded product is a foamed pipe joint (cheese) shown in FIG. 3, the length L2 from the receiving end 222a of the receiving portion 220a to the stopper 213a and the thickness in the vicinity of the stopper 213a of the receiving portion 220a
  • the ratio to the length d2 (hereinafter also referred to as “L2 / d2 ratio”) is the same as the L1 / d1 ratio described above.
  • the L2 / d2 ratio is the same as in the socket 220b of the foamed resin molded product 2.
  • the ratio of the length L3 from the receiving end 222c of the receiving portion 220c to the stopper 213c and the thickness d3 in the vicinity of the stopper 213c of the receiving portion 220c is the same as the L1 / d1 ratio described above.
  • the foamed resin molded article of the present invention is not limited to the above embodiment, and may be a foamed pipe joint having another shape such as a nipple or a valve socket. Further, the foamed resin molded product is not limited to the foamed pipe joint, and may be a lid made of a foamed resin manufactured by injection molding, a pipe made of a foamed resin manufactured by extrusion molding, or the like.
  • the foamed resin molded article of the present invention since the foamed resin molded article of the present invention has a foamed resin layer, it is excellent in heat insulation.
  • the content of the rubber component on the outer surface is smaller than that of a normal ABS resin or a normal AES resin. Therefore, the foamed resin molded article of the present invention is excellent in chemical resistance.
  • Examples 1 to 6 A resin composition obtained by kneading polymethyl methacrylate with an ABS resin was used as a non-foaming resin composition. At this time, the non-foamable resin composition was kneaded at a ratio such that the peak area ratio of each component obtained by measurement with PGC would be as shown in Table 2. A mixture of this non-foamable resin composition and azodicarbonamide as a foaming agent is injection-molded as a foamable resin composition, and the receiving part is made of a non-foaming resin layer and is solid, inside and outside of the receiving part DV joint with an inner diameter of 30 mm as shown in FIG.
  • Example 7 An elbow was manufactured in the same manner as in Example 6 except that the length of the socket was 13 mm.
  • Example 8 An elbow was manufactured in the same manner as in Example 1 except that the thickness between the inner and outer wall surfaces of the socket was 3.2 mm and the length of the socket was 30 mm.
  • Example 9 An elbow was produced in the same manner as in Example 1 except that the non-foamable resin composition was kneaded at a ratio such that the peak area ratio of each component obtained by measurement with PGC would be as shown in Table 3.
  • Example 10 An elbow was manufactured in the same manner as in Example 1 except that the thickness between the inner and outer wall surfaces of the socket was 2.6 mm and the length of the socket was 30 mm.
  • Example 11 An elbow was manufactured in the same manner as Example 6, except that the thickness between the inner and outer wall surfaces of the socket was 5.5 mm and the length of the socket was 18 mm.
  • Example 1 was repeated except that the ABS resin and polymethyl methacrylate were kneaded at a ratio such that the peak area ratio of each component obtained by measuring the non-foaming resin composition with PGC would be as shown in Table 3. An elbow was produced in the same manner.
  • the socket was cut into a dumbbell shape in the tube axis direction to obtain a test piece.
  • the obtained test piece is fixed to a bending jig manufactured so as to be subjected to a stretching stress of 3 MPa in a room at 23 ° C., and cotton of a size of 10 mm ⁇ 20 mm in which 2 mL of polyethylene glycol is immersed is the center of the test piece Placed on top of the department.
  • Three test pieces were prepared for each example, and after leaving any one of the three test pieces for 36 hours, cotton was removed and visually confirmed. The other two of the three test pieces were left for 72 hours and then cotton was removed for visual confirmation to evaluate their chemical resistance.
  • the chemical resistance was evaluated according to the following evaluation criteria for the presence or absence of cracks in the test pieces. The results are shown in Tables 2-3. (Evaluation criteria) ⁇ : No breakage or cracking occurred even after 72 hours. Fair: Breaking and cracking occurred in mounting time of 1 hour or more and less than 72 hours. X: There is breakage or cracking in less than 1 hour of mounting time.
  • the manufactured elbow 3 is connected to the pipe 40 using a hydraulic fatigue tester (series fatigue tester EHF-ED10-70L manufactured by Shimadzu Corporation) 300, and a fixing jig 60 and a fixing jig It was fixed at 62.
  • a stress F of 700 kgf (6865 N) was applied once per second, and the elbow 3 was pulled upward in the vertical direction to conduct a stretching fatigue test.
  • the stretch fatigue test was performed until the elbow 3 stretch-broken or stress F was applied 1000 times, and the number of times the stress F was applied until the elbow 3 stretch-broken was measured.
  • the elbow 3 had the same shape as the foamed resin molded product 1 shown in FIGS.
  • Stretch fatigue resistance was evaluated according to the following evaluation criteria. The results are shown in Tables 2-3. (Evaluation criteria) ⁇ : more than 1000 times. Fair: 200 or more and less than 1000 times. X: less than 200 times.
  • Example 1 to 4 As shown in Tables 2 to 3, in Examples 1 to 4 to which the present invention was applied, the evaluation of the chemical resistance was “o”, and it was found that the chemical resistance was excellent. Further, as a result of the stretching fatigue test, it was found that the film was provided with sufficient strength against stretching. Although Examples 5 to 7 and 9 in which the content of the rubber component (butadiene) in the non-foamed resin layer is 15% by mass or more are inferior to Examples 1 to 4, they were found to have chemical resistance and strength. It was found that Example 8 in which the length of the receiving part was long was inferior to Examples 1 to 4 but provided with a certain degree of strength.

Landscapes

  • Engineering & Computer Science (AREA)
  • General Engineering & Computer Science (AREA)
  • Chemical & Material Sciences (AREA)
  • Mechanical Engineering (AREA)
  • Polymers & Plastics (AREA)
  • Health & Medical Sciences (AREA)
  • Medicinal Chemistry (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Organic Chemistry (AREA)
  • Materials Engineering (AREA)
  • General Chemical & Material Sciences (AREA)
  • Manufacture Of Porous Articles, And Recovery And Treatment Of Waste Products (AREA)
  • Laminated Bodies (AREA)
  • Thermal Insulation (AREA)
  • Compositions Of Macromolecular Compounds (AREA)
  • Branch Pipes, Bends, And The Like (AREA)
  • Rigid Pipes And Flexible Pipes (AREA)
  • Injection Moulding Of Plastics Or The Like (AREA)

Abstract

ゴム成分とシアン化ビニル系単量体単位と芳香族ビニル系単量体単位とを含む共重合体である第一の樹脂と発泡剤とを含む発泡樹脂層（３０）と、発泡樹脂層（３０）を覆う非発泡樹脂層（５０）とを有し、非発泡樹脂層（５０）は、ゴム成分とシアン化ビニル系単量体単位と芳香族ビニル系単量体単位とを含む共重合体である第二の樹脂を含み、熱分解ガスクロマトグラフィー質量分析法（ＰＧＣ／ＭＳ）により求められる、非発泡樹脂層（５０）の前記ゴム成分の含有量が、前記第二の樹脂の総質量に対して１質量％以上３０質量％以下である発泡樹脂成形品（１）。

Description

発泡樹脂成形品
　本発明は、ドレンパイプ等の接続に用いられる発泡樹脂成形品に関する。
　本願は、２０１７年９月２９日に日本に出願された特願２０１７－１８９５６２号に基づき優先権を主張し、その内容をここに援用する。
　従来、鋼管や合成樹脂管からなる配管周りをグラスウール等の保温材で被覆することによって配管周りの結露等を防止するのが一般的である。
　しかし、上記従来の方法では、配管の作業とは別に、保温材を巻いたり被せたりする作業が必要であるため作業効率が悪く、狭い作業スペースでは作業を行えない場合もある。
　そこで、断熱層となる発泡樹脂層を有する樹脂製の配管や管継手が提案されている。断熱層を設けることにより、配管施工後に保温材で被覆しなくても結露の防止が可能となる。
　特許文献１には、本体部の内部に発泡樹脂からなる断熱層を備え、この断熱層を囲繞する本体部の内外壁と接続部とが、射出成形により一体成形された構成の断熱層付き管継手が提案されている。特許文献１の管継手に使用できる樹脂としては、ポリ塩化ビニル、アクリロニトリル－ブタジエン－スチレン共重合体（ＡＢＳ樹脂）、ポリエチレン、ポリプロピレン等が挙げられており、現行品では、耐衝撃性、耐熱性に優れるＡＢＳ樹脂が使用されている。
特許第３６９９５７９号公報
　ＡＢＳ樹脂は、初期性能として耐衝撃性、耐熱性に優れるが、耐薬品性に劣る。そのため、ＡＢＳ樹脂製の継手は、ドレン配管中に有機溶媒や油分が存在すると、本体部の内外壁が劣化し、断熱性が低下する虞がある。
　そこで、本発明は、断熱性及び耐薬品性に優れる発泡樹脂成形品を目的とする。
　鋭意検討を重ねた結果、本発明者等は、発泡樹脂成形品を構成するＡＢＳ樹脂等に含まれるブタジエン等のゴム成分の含有量を減らすと、耐薬品性を向上できることを見出した。
　加えて、アクリル樹脂を含有させると発泡樹脂成形品を透明にでき、配管と管継手との接続部分を視認しやすくできることを見出した。
　上記課題を解決するために、本発明は以下の態様を有する。
［１］ゴム成分とシアン化ビニル系単量体単位と芳香族ビニル系単量体単位とを含む共重合体である第一の樹脂と発泡剤とを含む発泡樹脂層と、前記発泡樹脂層を覆う非発泡樹脂層とを有し、
　前記非発泡樹脂層は、ゴム成分とシアン化ビニル系単量体単位と芳香族ビニル系単量体単位とを含む共重合体である第二の樹脂を含み、
　熱分解ガスクロマトグラフィー質量分析法（ＰＧＣ／ＭＳ）により求められる、前記非発泡樹脂層の前記ゴム成分の含有量が、前記第二の樹脂の総質量に対して１質量％以上３０質量％以下である発泡樹脂成形品。
［２］前記非発泡樹脂層は、アクリル樹脂をさらに含む、［１］に記載の発泡樹脂成形品。
　本発明の発泡樹脂成形品によれば、断熱性及び耐薬品性に優れる。
本発明の一実施形態に係る発泡樹脂成形品を示す側面図である。 図１に示す発泡樹脂成形品の縦断面図である。 本発明の他の実施形態に係る発泡樹脂成形品を示す部分断面図である。 伸縮疲労試験の配管構造を示す側面図である。
［発泡樹脂成形品］
　以下、本発明の実施の形態による発泡樹脂成形品について、図面に基づいて説明する。
　図１に示すように、本実施形態による発泡樹脂成形品１は、ドレンパイプの接続に使用される継手（一般的に「エルボ」（ｅｌｂｏｗ）と称されるＬ形の配管接合継手）を一例としている。発泡樹脂成形品１は、内部に屈曲する流路を有し、両端に開口部１２ａと開口部１２ｂとを有する本体部１０を備える。発泡樹脂成形品１は、本体部１０の開口部１２ａの周縁を囲む円筒状の受口部２０ａと、本体部１０の開口部１２ｂの周縁を囲む円筒状の受口部２０ｂとを備える。本体部１０と、受口部２０ａと、受口部２０ｂとは、一体に形成されている。
　図２は、図１に示す発泡樹脂成形品１の縦断面図である。図２に示すように、本体部１０は、発泡樹脂層３０と、非発泡樹脂層５０とを備える。発泡樹脂層３０の両面は、非発泡樹脂層５０に覆われている。受口部２０ａと受口部２０ｂとは、非発泡樹脂層５０で形成されている。発泡樹脂層３０は、その一部が受口部２０ａの非発泡樹脂層５０に食い込んでいる。また、発泡樹脂層３０は、その一部が受口部２０ｂの非発泡樹脂層５０に食い込んでいる。
　本体部１０の開口部１２ａの周縁には、ストッパー１３ａが形成されている。受口部２０ａの受口端部２２ａからストッパー１３ａまでの長さはＬ１である。
　受口部２０ａのストッパー１３ａ近傍の厚さはｄ１である。
　受口部２０ｂの構造は、受口部２０ａの構造と同様である。
　本発明の実施の形態による発泡樹脂成形品は、継手（一般的に「チーズ」（ｔｅｅｓ）と称される３方向分岐のＴ形の配管接合継手）であってもよい。
　図３に示すように、発泡樹脂成形品２は、第一の管軸Ｏ１と、第二の管軸Ｏ２を有する。二つの管軸Ｏ１及びＯ２は直線状であり互いに９０．０°～９１．１°の角度をなして交差する。
　発泡樹脂成形品２は、内部に流路（例えばドレンの流路）を有する管状の本体部２１０と、この本体部２１０の開口部に一体に形成された３つの受口部２２０ａと２２０ｂと２２０ｃとを有する。３つの受口部２２０ａ、２２０ｂ及び２２０ｃの内径は、発泡層付きの管部材を挿入接続するために、本体部２１０の内径よりも大径をなしている。
　発泡樹脂成形品２は、直管をなす本体部２１０の両端２１２ａ、２１２ｂ及び第二の管軸Ｏ２方向に開口する分岐端部２１２ｃの３箇所の開口部のそれぞれに受口部２２０ａ、２２０ｂ、２２０ｃが設けられたチーズ部材を構成している。
　本体部２１０において、第一の管軸Ｏ１を挟んで分岐端部２１２ｃに対向する位置には、成形時に射出される位置となる射出ゲート部２１４が設けられている。
　本体部２１０の開口端部２１２ａの周縁には、ストッパー２１３ａが形成され、本体部２１０の内周面に連接している。本体部２１０の分岐端部２１２ｃの周縁には、ストッパー２１３ｃが形成されている。
　本体部２１０は、発泡樹脂層２３０と、非発泡樹脂層２５０とを備える。発泡樹脂層２３０の両面は、非発泡樹脂層２５０に覆われている。受口部２２０ａと受口部２２０ｂと受口部２２０ｃとは、非発泡樹脂層２５０で形成されている。
　受口部２２０ａの受口端部２２２ａから本体部２１０の開口端部２１２ａまでの長さはＬ２である。長さＬ２は、受口端部２２２ａからストッパー２１３ａまでの長さと等しい。受口部２２０ａのストッパー２１３ａ近傍の厚さはｄ２である。受口部２２０ｂの構造は、受口部２２０ａの構造と同様である。すなわち、受口端部２２２ｂから開口端部２１２ｂまでの長さはＬ２である。
　また、受口部２２０ｃの受口端部２２２ｃから、本体部２１０の分岐端部２１２ｃまでの長さはＬ３である。長さＬ３は、受口端部２２２ｃからストッパー２１３ｃまでの長さと等しい。受口部２２０ｃのストッパー２１３ｃ近傍の厚さはｄ３である。
＜発泡樹脂層＞
　発泡樹脂層３０は、発泡性樹脂組成物を発泡し成形してなる。本発明の発泡樹脂成形品１は、発泡樹脂層３０を有することにより、断熱性に優れる。
　発泡樹脂層３０における発泡倍率は、１．０倍以上８．０倍以下が好ましく、１．１倍以上５．０倍以下がより好ましく、１．２倍以上３．０倍以下がさらに好ましい。
　発泡倍率を上記数値範囲内とすることにより、高い断熱性能を付与できる。
　発泡倍率は、樹脂の種類又は量、発泡剤の種類又は量、製造条件等により調整できる。
　なお、発泡倍率は以下の方法で測定できる。
（発泡倍率の測定方法）
　発泡樹脂成形品１の本体部１０から円周方向１０ｍｍ以上、軸方向５０ｍｍを切り出し、非発泡樹脂層５０をフライスで切削し、発泡樹脂層３０だけを長さ約５０ｍｍ程度の板状に加工したものを試験片とする。なお、試験片は円周方向に均等に４分割した点を中心に４個作成するものとする。
　ＪＩＳ　Ｋ　７１２２に従い、２３℃±２℃で水置換式比重測定器を用いて試験片の見かけ密度を小数点以下３桁まで求め、下記式（１）により発泡倍率を算出する。
　ｍ＝γｃ／γ　・・・（１）
［式（１）中、ｍは発泡倍率であり、γは発泡樹脂層の見かけ密度（ｇ／ｃｍ３）であり、γｃは発泡樹脂層の未発泡時の密度（ｇ／ｃｍ３）である。なお、発泡樹脂層の未発泡時の密度は、発泡樹脂層を溶融したものから測定できる。］
　発泡樹脂層３０においては、複数の気泡が形成されており、気泡壁には実質的に孔が存在せず、複数の気泡の少なくとも一部は、相互に連通していない独立気泡になっている。独立気泡率は８５％以上が好ましく、９０％以上がより好ましい。上限値は、特に限定されないが、実質的には９９％以下とされる。上記数値範囲内であれば、低い熱伝導率を長期に亘って保つことができ、断熱性により優れる。
　独立気泡率は、ＪＩＳ　Ｋ　７１３８：２００６に準拠して測定される。
＜発泡性樹脂組成物＞
　本実施形態の発泡性樹脂組成物は、ゴム成分とシアン化ビニル系単量体単位と芳香族ビニル系単量体単位とを含む共重合体である第一の樹脂と発泡剤とを含む。
　本明細書において、「単位」とは、重合前の単量体化合物（モノマー）に由来する構造部分をさし、例えば、「シアン化ビニル系単量体単位」とは「シアン化ビニルモノマー（アクリロニトリル）に由来する構造部分」をさす。重合体中の各単量体単位の含有割合は、当該重合体の製造に用いた単量体混合物中の該単量体の含有割合に該当する。
　また、「（メタ）アクリル」とは「アクリル」と「メタクリル」の一方又は双方をさし、「アクリロニトリル」とは「アクリロニトリル」と「メタクリロニトリル」の一方又は双方をさす。
（第一の樹脂）
　第一の樹脂は、ゴム成分とシアン化ビニル系単量体単位と芳香族ビニル系単量体単位とを含む共重合体である。
　ゴム成分とシアン化ビニル系単量体単位と芳香族ビニル系単量体単位とを含む共重合体は、ゴム成分の存在下で、芳香族ビニル系単量体とシアン化ビニル系単量体とを重合して得られる樹脂である。
　本明細書において、ゴム成分とは、ポリブタジエンやポリイソプレン等のジエン系ゴムの原料やアクリルゴムの原料となるモノマー成分のことをいう。
　ゴム成分としては、ジエン系ゴムであればブタジエン、イソプレン、エチレン、プロピレン等のジエン系ゴムのモノマー又はその重合体が挙げられ、アクリルゴムであればアクリル酸エチル、アクリル酸ブチル、アクリル酸ブトキシエチル、及び、アクリル酸メトキシエチル等のアクリル酸エステルモノマー又はその重合体が挙げられる。
　シアン化ビニル系単量体としては、アクリロニトリル、メタアクリロニトリル等が挙げられ、アクリロニトリルが好ましい。
　芳香族ビニル系単量体としては、スチレン、α－メチルスチレン、β－メチルスチレン、４－メチルスチレン、β－ブロモスチレン等が挙げられ、スチレン、α－メチルスチレンが好ましい。
　第一の樹脂の具体例としては、アクリロニトリル－ブタジエン－スチレン共重合体（ＡＢＳ樹脂）、アクリロニトリル－エチレンプロピレンジエン－スチレン共重合体（ＡＥＳ樹脂）、アクリロニトリル－アクリルゴム－スチレン共重合体（ＡＡＳ樹脂）等が挙げられ、さらにこれらを混合したものとしてもよい。
　第一の樹脂のゴム成分の含有量は、特に限定されず、第一の樹脂の総質量に対して１質量％以上３０質量％以下が好ましい。
　第一の樹脂は、シアン化ビニル系単量体単位の含有量が、第一の樹脂の総質量に対して１０質量％以上５０質量％以下が好ましく、１５質量％以上４５質量％以下がより好ましい。シアン化ビニル系単量体単位の含有量が上記下限値以上であると、引張強さを向上させることができる。シアン化ビニル系単量体単位の含有量が上記上限値以下であると、衝撃強さを向上させることができる。
　第一の樹脂は、芳香族ビニル系単量体単位の含有量が、第一の樹脂の総質量に対して１５質量％以上６０質量％以下が好ましく、２０質量％以上５０質量％以下がより好ましい。芳香族ビニル系単量体単位の含有量が上記下限値以上であると、押込み硬さを向上させることができる。芳香族ビニル系単量体単位の含有量が上記上限値以下であると、衝撃強さを向上させることができる。
　第一の樹脂は、シアン化ビニル系単量体単位、及び芳香族ビニル系単量体単位以外の任意の単量体単位を含んでいてもよく、その例としてはポリカーボネート樹脂やそのモノマーが挙げられる。
　第一の樹脂における各成分の含有量は、熱分解ガスクロマトグラフィー質量分析法（ＰＧＣ／ＭＳ）を用いた分析により求められる。
　以下にＰＧＣ／ＭＳを用いた測定条件の例を示す。
［測定条件］
・装置
　熱分解装置：ＰＹ－２０２０ｉＤ（フロンティア・ラボ）。
　ガスクロマトグラフ：ＧＣ ２０１０（島津製作所）。
　質量分析装置：ＧＣＭＳ－ＱＰ ２０１０（島津製作所）。
・熱分解条件
　熱分解温度：５５０℃。
　インターフェース温度：２５０℃。
・ガスクロマトグラフ条件。
　キャリアー流量：１ｍｌ/ｍｉｎ（Ｈｅ）。
　スプリット比：１００:１。
　分離カラム：ＤＢ－１（１．００μｍ、０．２５ｍｍφ×３０ｍ）。
　オーブン温度：４０℃（３ｍｉｎ）－３２０℃（１０ｍｉｎ）。
・質量分析条件
　インターフェース温度：２５０℃。
　イオン化温度：２２０℃。
　マスレンジ：２８～７００ｍ/ｚ。
　電圧：１．２ｋＶ。
　ＰＧＣ／ＭＳの測定により第一の樹脂における各成分の含有量を算出する方法について説明する。
　まず、第一の樹脂を構成する各成分を熱分解ガスクロマトグラフィーにより熱分解・分離し、各成分がピークとして記録された熱分解パターン（パイログラム）を得る。次に、熱分解パターンの各ピークについて、質量分析装置により得られるマススペクトルによってアクリロニトリル、ゴム成分、スチレンの各成分を特定する。
　ここで、アクリロニトリル、ゴム成分、スチレンの各成分は熱分解による解重合率（重合体が単量体に分解する割合）が異なるため、パイログラムにおける各ピークの面積（Ｘ）を、熱分解による各成分の解重合率（Ｙ）で割ったものを各成分のピーク面積（Ｚ）とする。各成分の解重合率（Ｙ）は、アクリロニトリル：０．１５、ゴム成分：０．１０、スチレン：１．０である。また、例えば、他の樹脂としてポリメタクリル酸メチル等のアクリル樹脂を含む場合、アクリル樹脂の解重合率は１．０である。
　そして、熱分解パターンの各成分のピーク面積（Ｚ）の総和（Ｔ）に対する比率（Ｚ／Ｔ）を、第一の樹脂における各成分の含有量（質量％）とする。
　表１に、アクリル樹脂を含むアクリロニトリル－ブタジエン－スチレン共重合体（ＡＢＳ樹脂）をＰＧＣ／ＭＳ測定して得られる各成分の含有量の一例を示す。表１において、「保持時間」は、各成分が熱分解してパイログラムのピークとして現れる時間を意味する。「サンプル量」は、分析に供したＡＢＳ樹脂の質量である。
Figure JPOXMLDOC01-appb-T000001
　発泡性樹脂組成物において、発泡性樹脂組成物の総質量に対する第一の樹脂の含有量は、４５質量％以上９０質量％以下が好ましく、５０質量％以上８５質量％以下がより好ましい。
　本実施形態の発泡性樹脂組成物は、第一の樹脂以外の他の樹脂を含有してもよい。
　他の樹脂としては、例えば、ポリアクリル酸メチル、ポリアクリル酸エチル、ポリアクリル酸グリシジル、ポリメタクリル酸メチル、ポリメタクリル酸エチル、ポリメタクリル酸グリシジル等のアクリル樹脂、ポリビニル樹脂、ポリエステル樹脂、ポリエーテル樹脂、ポリイミド樹脂等が挙げられる。これらは単独で用いられてもよく、２種類以上が併用されても良い。
　発泡性樹脂組成物において、第一の樹脂の含有量は、発泡性樹脂組成物中の樹脂の総質量に対して、７０質量％以上１００質量％以下が好ましく、８５質量％以上１００質量％以下がより好ましい。
（発泡剤）
　発泡剤としては、揮発性発泡剤、分解型発泡剤のいずれを使用してもよい。
　揮発性発泡剤としては、例えば脂肪族炭化水素、脂環族炭化水素、ハロゲン化炭化水素、エーテル、ケトン等が挙げられる。このうち脂肪族炭化水素としては、例えばプロパン、ブタン（ノルマルブタン、イソブタン）、ペンタン（ノルマルペンタン、イソペンタンなど）等が挙げられ、脂環族炭化水素としては、例えばシクロペンタン、シクロへキサン等が挙げられる。ハロゲン化炭化水素としては、例えばトリクロロフルオロメタン、トリクロロトリフルオロエタン、テトラフルオロエタン、クロロジフルオロエタン、ジフルオロエタン等のハロゲン化炭化水素などの１種または２種以上が挙げられる。さらにエーテルとしては、例えばジメチルエーテル、ジエチルエーテル等が挙げられ、ケトンとしては、例えばアセトン、メチルエチルケトン等が挙げられる。
　分解型発泡剤としては、例えば重炭酸ナトリウム（炭酸水素ナトリウム）、炭酸ナトリウム、重炭酸アンモニウム、亜硝酸アンモニウム、アジド化合物、ホウ水素化ナトリウムなどの無機系発泡剤、アゾジカルボンアミド、アゾジカルボン酸バリウム、ジニトロソペンタメチレンテトラミンなどの有機系発泡剤が挙げられる。
　その他、炭酸ガス、窒素、空気等のガスを発泡剤として用いてもよい。
　発泡性能に優れる観点から、分解型発泡剤が好ましく、中でも重曹、アゾジカルボンアミドがより好ましい。
　これらは単独で用いられても良く、２種以上が併用されてもよい。
　発泡剤の含有量は、第一の樹脂１００質量部に対して、０．１質量部以上８質量部以下が好ましく、１質量部以上５質量部以下がより好ましく、１質量部以上３質量部以下がさらに好ましい。
　本発明の発泡性樹脂組成物は、本発明の効果を損なわない範囲で、第一の樹脂、発泡剤、以外の他の成分（任意成分）を含んでもよい。
　任意成分の含有量は、第一の樹脂１００質量部に対して、５０質量部以下が好ましく、３０質量部以下がより好ましく、２０質量部以下がさらに好ましい。
　本発明の発泡性樹脂組成物は、第一の樹脂、発泡剤、及び任意成分を含むことができる。発泡性樹脂組成物は、全成分が予め混合された混合物でもよく、全成分の一部又は全部を成形機内で混合する形態でもよい。全成分を予め混合した混合物は粉状でもよく、ペレット状でもよい。
＜非発泡樹脂層＞
　本実施形態の非発泡樹脂層は、非発泡性樹脂組成物を成形してなる。本発明の発泡樹脂成形品は、非発泡樹脂層を有することにより、発泡樹脂成形品の強度を高めることができる。
　非発泡樹脂層は、発泡樹脂層を覆っている。
＜非発泡性樹脂組成物＞
　本実施形態の非発泡性樹脂組成物は、ゴム成分とシアン化ビニル系単量体単位と芳香族ビニル系単量体単位とを含む共重合体である第二の樹脂を含む。
（第二の樹脂）
　第二の樹脂は、ゴム成分とシアン化ビニル系単量体単位と芳香族ビニル系単量体単位とを含む共重合体である。
　第二の樹脂は、第一の樹脂と同じであってもよく、異なっていてもよい。
第二の樹脂は、ゴム成分の含有量が、第二の樹脂の総質量に対して１質量％以上３０質量％以下であり、１質量％以上２５質量％以下が好ましく、３質量％以上２０質量％以下がより好ましく、５質量％以上１５質量％以下がさらに好ましく、５質量％以上１０質量％以下が特に好ましい。ゴム成分の含有量が上記下限値以上であると、発泡樹脂成形品の強度を高めやすい。ゴム成分の含有量が上記上限値以下であると、耐薬品性をより向上しやすい。
　第二の樹脂は、シアン化ビニル系単量体単位の含有量が、第二の樹脂の総質量に対して１０質量％以上５０質量％以下が好ましく、１５質量％以上４５質量％以下がより好ましい。シアン化ビニル系単量体単位の含有量が上記下限値以上であると、引張強さを向上させることができる。シアン化ビニル系単量体単位の含有量が上記上限値以下であると、衝撃強さを向上させることができる。
　第二の樹脂は、芳香族ビニル系単量体単位の含有量が、第二の樹脂の総質量に対して１５質量％以上６０質量％以下が好ましく、２０質量％以上５０質量％以下がより好ましい。芳香族ビニル系単量体単位の含有量が上記下限値以上であると、押込み硬さを向上させることができる。芳香族ビニル系単量体単位の含有量が上記上限値以下であると、衝撃強さを向上させることができる。
　第二の樹脂における各成分の含有量は、熱分解ガスクロマトグラフィー質量分析法（ＰＧＣ／ＭＳ）を用いた分析により求められる。測定条件としては、第一の樹脂と同様の条件で測定できる。
　非発泡性樹脂組成物において、非発泡性樹脂組成物の総質量に対する第二の樹脂の含有量は、４５質量％以上９０質量％以下が好ましく、５０質量％以上８５質量％以下がより好ましい。
　本実施形態の非発泡性樹脂組成物は、第二の樹脂以外の他の樹脂を含有してもよい。
　他の樹脂としては、例えば、ポリビニル樹脂、ポリエステル樹脂、ポリエーテル樹脂、アクリル樹脂、ポリイミド樹脂等が挙げられる。これらは単独で用いられてもよく、２種類以上が併用されても良い。
　本実施形態の非発泡性樹脂組成物は、アクリル樹脂をさらに含有することが好ましい。アクリル樹脂としては、例えば、アクリル酸エステルの重合体やメタクリル酸エステルの重合体が挙げられる。アクリル酸エステルの重合体としては、ポリアクリル酸メチル、ポリアクリル酸エチル、ポリアクリル酸グリシジル等が挙げられる。メタクリル酸エステルの重合体としては、ポリメタクリル酸メチル、ポリメタクリル酸エチル、ポリメタクリル酸グリシジル等が挙げられる。
　アクリル樹脂の含有量は、非発泡性樹脂組成物中の樹脂の総質量に対して、２０質量％以上６０質量％以下が好ましく、３０質量％以上５０質量％以下がより好ましい。アクリル樹脂の含有量が上記数値範囲内であると、発泡樹脂成形品の強度及び透明度を高めやすい。
　アクリル樹脂の含有量は、非発泡性樹脂組成物の総質量に対して、１０質量％以上５５質量％以下が好ましく、２０質量％以上５０質量％以下がより好ましい。
　第二の樹脂とその他の樹脂を含有する非発泡性樹脂組成物における各成分の含有量は、熱分解ガスクロマトグラフィー質量分析法（ＰＧＣ／ＭＳ）を用いた分析により求められる。測定条件としては、第一の樹脂と同様の条件で測定できる。第二の樹脂における各成分の含有量は、第一の樹脂における各成分の含有量と同一の算出方法で算出できる。
　なお、アクリロニトリル、ゴム成分、スチレン、アクリル樹脂の解重合率は、アクリロニトリル：０．１５、ゴム成分：０．１０、スチレン：１．０、アクリル樹脂：１．０である。
　非発泡性樹脂組成物において、第二の樹脂の含有量は、非発泡性樹脂組成物中の樹脂の総質量に対して、４０質量％以上１００質量％以下が好ましく、４５質量％以上１００質量％以下がより好ましく、５０質量％以上１００質量％以下がさらに好ましい。
　本実施形態の非発泡性樹脂組成物は、本発明の効果を損なわない範囲で、第二の樹脂以外の他の成分（任意成分）を含んでもよい。
　任意成分としては、着色剤、難燃剤、酸化防止剤、紫外線吸収剤、光安定剤等が挙げられる。
　任意成分の含有量は、第二の樹脂１００質量部に対して、５０質量部以下が好ましく、３０質量部以下がより好ましく、２０質量部以下がさらに好ましい。
　なお、非発泡樹脂層は、前記発泡剤を含んでいる必要はないが、前記発泡剤を含んでいてもよい。非発泡樹脂層に含まれる発泡剤の量は、第二の樹脂１００質量部に対して、０質量部以上８質量部以下が好ましく、０質量部以上５質量部以下がより好ましく、０質量部以上３質量部以下がさらに好ましい。また、非発泡樹脂層における発泡倍率は、０倍であることが好ましいが、１．５倍以下で低発泡しているものも本発明から排除されない。
　本実施形態の非発泡性樹脂組成物は、第二の樹脂及び任意成分を含むことができる。非発泡性樹脂組成物は、全成分が予め混合された混合物でもよく、全成分の一部又は全部を成形機内で混合する形態でもよい。全成分を予め混合した混合物は粉状でもよく、ペレット状でもよい。
　本実施形態の非発泡性樹脂組成物は、非発泡樹脂層を形成し、本発明の発泡樹脂成形品の外表面を覆っている。加えて、本実施形態の非発泡性樹脂組成物は、第二の樹脂におけるゴム成分の含有量が、第二の樹脂の総質量に対して１質量％以上３０質量％以下である。そのため、非発泡樹脂層は耐薬品性に優れ、本発明の発泡樹脂成形品は耐薬品性に優れる。
＜発泡樹脂成形品の製造方法＞
　発泡樹脂成形品は、射出成形又は押出成形により製造される。
　例えば、発泡性樹脂組成物を加熱溶融して金型内に射出し、任意の時間任意の温度で加熱し、任意の時間任意の温度で冷却することによって、所定の発泡倍率を有する発泡樹脂成形品が得られる。
　押出成形の場合は、発泡性樹脂組成物を加熱溶融して押出機から金型内に注入し、任意の時間任意の温度で加熱することにより発泡性樹脂組成物を発泡・成形させる。任意の時間任意の温度で冷却した後に、所定の長さに切断することにより、所定の発泡倍率を有する発泡樹脂成形品が得られる。
　射出成形機において、金型内に射出される直前の発泡性樹脂組成物の温度（成形温度）は２００℃以上２８０℃以下が好ましく、２２０℃以上２６０℃以下がより好ましい。成形温度が前記範囲内であると熱可塑性樹脂の熱分解を抑えて透明性の低下を防ぎ、また、充分に溶融させて、発泡性樹脂組成物の良好な流動性が得られる。
　金型で成形するときの時間は、１分以上１０分以下が好ましい。前記下限値以上であれば、十分に硬化させることができ、前記上限値以下であれば、発泡樹脂成形品の生産性を向上しやすい。
　以上、本発明の発泡樹脂成形品について、詳細に説明してきたが、本発明は上記の一実施形態に限定されるものではなく、その趣旨を逸脱しない範囲で適宜変更可能である。
　例えば、発泡樹脂成形品は、非発泡樹脂層を有さず、発泡樹脂層のみであってもよい。その場合、発泡樹脂層は、ゴム成分の含有量が、第一の樹脂の総質量に対して１質量％以上３０質量％以下であればよい。発泡樹脂成形品が、発泡樹脂層のみで形成される場合、発泡樹脂層の外表面は、非発泡樹脂層と同様に高密度の層を形成していればよい。
　本発明の発泡樹脂成形品は、発泡樹脂層で形成されていればよく、さらに異なる他の樹脂層を有する多層成形品であってもよい。他の樹脂層としては、非発泡樹脂層の他、外面と同じ発泡樹脂層、外面とは異なる発泡樹脂層が挙げられる。これらの樹脂層の原料となる樹脂は、外面を形成する発泡樹脂層と同じ熱可塑性樹脂であってもよく、異なる熱可塑性樹脂であってもよい。樹脂層間の剥離を抑制する観点から、これらの樹脂層の原料となる樹脂は、外面を形成する発泡樹脂層と同じ熱可塑性樹脂であることが好ましい。
　発泡樹脂成形品が、図２に示す発泡管継手（エルボ）である場合、受口部２０ａの受口端部２２ａからストッパー１３ａまでの長さＬ１と、受口部２０ａのストッパー１３ａ近傍の厚さｄ１との比（以下、「Ｌ１／ｄ１比」ともいう。）は、３．５以上１０以下が好ましく、４．０以上９．０以下がより好ましく、４．５以上８．０以下がさらに好ましい。
　Ｌ１／ｄ１比が上記下限値以上であると、受口部２０ａに発泡樹脂層３０が侵入することを抑制しやすく、受口部２０ａの強度の低下を抑制しやすい。このため、発泡管継手が伸び縮みによる伸縮疲労により破壊されにくくなる。加えて、Ｌ１／ｄ１比が上記下限値以上であると、受口部２０ａの長さＬ１が充分長いため、発泡管継手に挿入する配管等の挿入不足による漏水を抑制しやすい。
　Ｌ１／ｄ１比が上記上限値以下であると、厚さｄ１が充分厚く、発泡管継手が伸び縮みによる伸縮疲労により破壊されにくくなる。加えて、Ｌ１／ｄ１比が上記上限値以下であると、長さＬ１が長過ぎず、伸び縮みによる応力が受口部２０ａの根元に集中することを抑制しやすく、発泡管継手が伸び縮みによる伸縮疲労により破壊されにくくなる。
　なお、Ｌ１／ｄ１比は、発泡樹脂成形品１の受口部２０ｂにおいても同様である。
　発泡樹脂成形品が、図３に示す発泡管継手（チーズ）である場合、受口部２２０ａの受口端部２２２ａからストッパー２１３ａまでの長さＬ２と、受口部２２０ａのストッパー２１３ａ近傍の厚さｄ２との比（以下、「Ｌ２／ｄ２比」ともいう。）は、上述したＬ１／ｄ１比と同様である。
　Ｌ２／ｄ２比は、発泡樹脂成形品２の受口部２２０ｂにおいても同様である。
　また、受口部２２０ｃの受口端部２２２ｃからストッパー２１３ｃまでの長さＬ３と、受口部２２０ｃのストッパー２１３ｃ近傍の厚さｄ３との比は、上述したＬ１／ｄ１比と同様である。
　本発明の発泡樹脂成形品としては、上述の実施形態に限定されず、ニップルやバルブソケット等、他の形状を有する発泡管継手であってもよい。
　また、発泡樹脂成形品としては、発泡管継手に限定されず、射出成形によって製造される発泡樹脂製の蓋や、押出成形によって製造される発泡樹脂製の配管等であってもよい。
　以上、説明してきたように、本発明の発泡樹脂成形品は、発泡樹脂層を有するため、断熱性に優れる。加えて、本発明の発泡樹脂成形品は、外表面におけるゴム成分の含有量が、通常のＡＢＳ樹脂や通常のＡＥＳ樹脂と比べて少ない。そのため、本発明の発泡樹脂成形品は、耐薬品性に優れる。
　次に、実施例により本発明をさらに詳細に説明するが、本発明はこれら実施例に限定されるものではない。
　各実施例及び比較例で使用した原料、評価方法は、以下の通りである。
［使用原料］
＜第一の樹脂＞
　ＡＢＳ樹脂（ブタジエン含有量１５質量％）。
＜第二の樹脂＞
　ＡＢＳ樹脂（表２～３に記載の組成のＡＢＳ樹脂）。
＜他の樹脂＞
　アクリル樹脂（ポリメタクリル酸メチル）。
＜発泡剤＞
　ＡＤＣＡ（大塚化学社製、商品名「ＡＺ－ＨＭ」、アゾジカルボンアミド）。
［実施例１～６］
　ＡＢＳ樹脂にポリメタクリル酸メチルを混練した樹脂組成物を非発泡性樹脂組成物とした。このとき、非発泡性樹脂組成物をＰＧＣで測定して得られた各成分のピーク面積比が表２となる様な比率で混練した。この非発泡性樹脂組成物に発泡剤としてアゾジカルボンアミドを混合したものを発泡性樹脂組成物として、射出成形して、受口部が非発泡樹脂層からなり中実で、受口部の内外壁面間の厚みが３ｍｍ、受口部の長さが２３ｍｍ、本体部の内外壁間の厚みが８ｍｍ、発泡倍率２．０倍の発泡樹脂層を有する図２に示すような内径３０ｍｍのＤＶ継手タイプのエルボを製造した。
［実施例７］
　受口部の長さを１３ｍｍとした以外は、実施例６と同様にしてエルボを製造した。
［実施例８］
　受口部の内外壁面間の厚みを３．２ｍｍ、受口部の長さを３０ｍｍとした以外は、実施例１と同様にしてエルボを製造した。
［実施例９］
　非発泡性樹脂組成物をＰＧＣで測定して得られた各成分のピーク面積比が表３となる様な比率で混練したこと以外は、実施例１と同様にしてエルボを製造した。
［実施例１０］
　受口部の内外壁面間の厚みを２．６ｍｍ、受口部の長さを３０ｍｍとした以外は、実施例１と同様にしてエルボを製造した。
［実施例１１］
　受口部の内外壁面間の厚みを５．５ｍｍ、受口部の長さを１８ｍｍとした以外は、実施例６と同様にしてエルボを製造した。
［比較例１、２］
　ＡＢＳ樹脂とポリメタクリル酸メチルとを、非発泡性樹脂組成物をＰＧＣで測定して得られた各成分のピーク面積比が表３となる様な比率で混練したこと以外は、実施例１と同様にしてエルボを製造した。
［耐薬品性の評価］
　上記実施例、比較例で得られたエルボのそれぞれについて、受口部を管軸方向にダンベル形状に切り取って試験片を得た。得られた試験片を、２３℃の室内において、３ＭＰａの伸縮応力がかかるように作製された曲げ治具に固定し、ポリエチレングリコール２ｍＬを浸漬した１０ｍｍ×２０ｍｍの大きさの綿を試験片の中央部の上に載置した。試験片は各例につき３個作製し、３個の試験片のうち任意の１個を３６時間放置した後に綿を外して目視で確認した。３個の試験片のうち他の２個は、７２時間放置した後に綿を外して目視で確認して耐薬品性の評価を行った。耐薬品性の評価は、試験片の割れの有無を下記評価基準に従って行った。結果を表２～３に示す。
（評価基準）
　○：７２時間経過後でも破断、クラックの発生なし。
　△：載置時間１時間以上７２時間未満で破断、クラックの発生あり。
　×：載置時間１時間未満で破断、クラックの発生あり。
［伸縮疲労耐性の評価］
　図４に示すように、油圧疲労試験機（島津製作所社製　一連型疲労試験機　ＥＨＦ－ＥＤ１０－７０Ｌ）３００を用い、製造したエルボ３をパイプ４０に接続し、固定治具６０及び固定治具６２に固定した。１秒間に１回、７００ｋｇ重（６８６５Ｎ）の応力Ｆをかけて、エルボ３を鉛直方向上向きに引っ張り、伸縮疲労試験を行った。伸縮疲労試験は、エルボ３が伸縮破断するか、応力Ｆを１０００回かけるまで行い、エルボ３が伸縮破断するまでの応力Ｆをかける回数を測定した。なお、エルボ３は、図１、２に示す発泡樹脂成形品１と同様の形状であった。伸縮疲労耐性は、下記評価基準に従って評価した。結果を表２～３に示す。
（評価基準）
　○：１０００回以上。
　△：２００回以上１０００回未満。
　×：２００回未満。
Figure JPOXMLDOC01-appb-T000002
Figure JPOXMLDOC01-appb-T000003
　表２～３に示すように、本発明を適用した実施例１～４は、耐薬品性の評価が「○」で、耐薬品性に優れることが分かった。また、伸縮疲労試験の結果、伸縮に対しても充分な強度を備えていることが分かった。
　非発泡樹脂層におけるゴム成分（ブタジエン）の含有量が１５質量％以上の実施例５～７、９は、実施例１～４に劣るものの、耐薬品性と強度とを備えることが分かった。
　受口部の長さが長い実施例８は、実施例１～４に劣るものの、ある程度の強度を備えることが分かった。
　実施例１０及び１１は、非発泡樹脂層におけるゴム成分（ブタジエン）の含有量が３０質量％以下であるため耐薬品性は充分であったが、Ｌ１／ｄ１比が上記した好ましい範囲外であったため、伸縮疲労耐性が劣る結果となった。
　一方、ゴム成分の含有量が本発明の範囲外である比較例１～２は、耐薬品性に劣るものであった。
　本発明の発泡樹脂成形品によれば、断熱性及び耐薬品性に優れることが分かった。
　１、２　発泡樹脂成形品
　３　エルボ
　１０、２１０　本体部
　１２ａ、１２ｂ　開口部
　１３ａ、２１３ａ、２１３ｃ　ストッパー
　２０ａ、２０ｂ、２２０ａ、２２０ｂ、２２０ｃ　受口部
　２２ａ、２２２ａ、２２２ｂ、２２２ｃ　受口端部
　２１２ａ、２１２ｂ　開口端部
　２１２ｃ　分岐端部
　３０、２３０　発泡樹脂層
　５０、２５０　非発泡樹脂層
　４０　パイプ
　６０、６２　固定治具
　３００　油圧疲労試験機

Claims (2)

  1. 　ゴム成分とシアン化ビニル系単量体単位と芳香族ビニル系単量体単位とを含む共重合体である第一の樹脂と発泡剤とを含む発泡樹脂層と、前記発泡樹脂層を覆う非発泡樹脂層とを有し、
    　前記非発泡樹脂層は、ゴム成分とシアン化ビニル系単量体単位と芳香族ビニル系単量体単位とを含む共重合体である第二の樹脂を含み、
    　熱分解ガスクロマトグラフィー質量分析法（ＰＧＣ／ＭＳ）により求められる、前記非発泡樹脂層の前記ゴム成分の含有量が、前記第二の樹脂の総質量に対して１質量％以上３０質量％以下である発泡樹脂成形品。
  2. 　前記非発泡樹脂層は、アクリル樹脂をさらに含む、請求項１に記載の発泡樹脂成形品。
PCT/JP2018/035921 2017-09-29 2018-09-27 発泡樹脂成形品 Ceased WO2019065834A1 (ja)

Priority Applications (7)

Application Number Priority Date Filing Date Title
KR1020207008352A KR102567701B1 (ko) 2017-09-29 2018-09-27 발포 관 조인트 및 배관 구조
SG11202002766WA SG11202002766WA (en) 2017-09-29 2018-09-27 Foamed resin molded article
JP2019524297A JP6581749B2 (ja) 2017-09-29 2018-09-27 発泡管継手及び配管構造
MYPI2020001617A MY200401A (en) 2017-09-29 2018-09-27 Foamed pipe joint and piping structure
US16/650,164 US11530309B2 (en) 2017-09-29 2018-09-27 Foamed resin molded article
CN201880062617.2A CN111315574B (zh) 2017-09-29 2018-09-27 发泡树脂成形品
PH1/2020/550129A PH12020550129B1 (en) 2017-09-29 2018-09-27 Foamed resin molded article

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
JP2017189562 2017-09-29
JP2017-189562 2017-09-29

Publications (1)

Publication Number Publication Date
WO2019065834A1 true WO2019065834A1 (ja) 2019-04-04

Family

ID=65902874

Family Applications (1)

Application Number Title Priority Date Filing Date
PCT/JP2018/035921 Ceased WO2019065834A1 (ja) 2017-09-29 2018-09-27 発泡樹脂成形品

Country Status (8)

Country Link
US (1) US11530309B2 (ja)
JP (3) JP6581749B2 (ja)
KR (1) KR102567701B1 (ja)
CN (1) CN111315574B (ja)
MY (1) MY200401A (ja)
PH (1) PH12020550129B1 (ja)
SG (1) SG11202002766WA (ja)
WO (1) WO2019065834A1 (ja)

Cited By (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
WO2020196318A1 (ja) * 2019-03-22 2020-10-01 積水化学工業株式会社 管継手及び配管構造
JP2022048587A (ja) * 2020-09-15 2022-03-28 積水化学工業株式会社 管継手、配管構造、及び管継手の製造方法
JP2022052156A (ja) * 2020-09-23 2022-04-04 積水化学工業株式会社 管継手

Families Citing this family (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JP7512147B2 (ja) * 2020-09-23 2024-07-08 積水化学工業株式会社 管継手

Citations (8)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS4847943A (ja) * 1971-10-14 1973-07-07
JPS6245639A (ja) * 1985-08-23 1987-02-27 Sumitomo Chem Co Ltd 熱可塑性樹脂組成物
JPH05202275A (ja) * 1992-01-29 1993-08-10 Teijin Ltd 熱可塑性樹脂組成物
JPH1149828A (ja) * 1997-08-04 1999-02-23 Techno Polymer Kk 耐シクロペンタン性に優れたゴム含有スチレン系樹脂および成形品
JP2002194108A (ja) * 2000-12-26 2002-07-10 Tsutsunaka Plast Ind Co Ltd 加圧下で加熱積層されるａｂｓ系樹脂シートおよびその積層シートと製造方法。
JP3699579B2 (ja) * 1998-01-13 2005-09-28 積水化学工業株式会社 断熱層付き管継手およびその製造方法
JP2010116478A (ja) * 2008-11-13 2010-05-27 Shin Kobe Electric Mach Co Ltd 断熱パネル用熱可塑性樹脂シート及び断熱パネル
WO2016068303A1 (ja) * 2014-10-30 2016-05-06 旭ファイバーグラス株式会社 透明ａｂｓ樹脂組成物

Family Cites Families (20)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS4731420U (ja) 1971-04-20 1972-12-08
JPS4915796A (ja) 1972-05-29 1974-02-12
JPS4952852A (ja) 1972-09-20 1974-05-22
JPS522275A (en) * 1975-06-24 1977-01-08 Iwatsu Electric Co Ltd Device of forming semiconductor substrates
JPS559412A (en) 1978-07-06 1980-01-23 Agency Of Ind Science & Technol Output controlling method for thin film destribution feedback laser
US4322260A (en) * 1979-04-04 1982-03-30 Monsanto Company Process for the continuous extrusion forming of a plastic double-walled foam-core conduit
US4440825A (en) * 1982-08-09 1984-04-03 Uniroyal, Inc. Laminate with skin based on AES graft copolymer
DE4414762B4 (de) 1993-04-28 2009-02-12 Mitsubishi Rayon Co., Ltd. Thermoplastische Harzzusammensetzung
JP3374947B2 (ja) 1994-12-08 2003-02-10 電気化学工業株式会社 透明永久帯電防止性樹脂組成物
JP3639051B2 (ja) 1996-07-11 2005-04-13 株式会社ジェイエスピー 発泡性樹脂粒子及びそれからなる発泡樹脂粒子、発泡成形体
JP4200074B2 (ja) 2003-10-03 2008-12-24 アロン化成株式会社 分岐用継手
JP2005298776A (ja) 2004-04-16 2005-10-27 Denki Kagaku Kogyo Kk 耐熱付与材、それを用いた樹脂組成物
US20060249216A1 (en) * 2005-05-03 2006-11-09 Sexton Earl H Co-injected pipe fitting
JP2007198534A (ja) 2006-01-27 2007-08-09 Sekisui Chem Co Ltd 管継手
JP2007333067A (ja) 2006-06-14 2007-12-27 Sekisui Chem Co Ltd 管継手
CN1986635B (zh) * 2006-12-21 2010-05-19 中化国际（苏州）新材料研发有限公司 一种采用连续本体法制备挤出级丙烯腈-丁二烯-苯乙烯接枝共聚物的方法
CN101058624B (zh) * 2007-05-16 2011-06-15 中国中化股份有限公司 一种连续本体法制备耐热abs聚合物的方法
JP2011002012A (ja) 2009-06-18 2011-01-06 Sekisui Chem Co Ltd 管継手部構造
JP5548107B2 (ja) 2010-11-16 2014-07-16 積水化学工業株式会社 断熱層付き管継手
JP6709079B2 (ja) 2016-03-02 2020-06-10 積水化学工業株式会社 発泡管継手

Patent Citations (8)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS4847943A (ja) * 1971-10-14 1973-07-07
JPS6245639A (ja) * 1985-08-23 1987-02-27 Sumitomo Chem Co Ltd 熱可塑性樹脂組成物
JPH05202275A (ja) * 1992-01-29 1993-08-10 Teijin Ltd 熱可塑性樹脂組成物
JPH1149828A (ja) * 1997-08-04 1999-02-23 Techno Polymer Kk 耐シクロペンタン性に優れたゴム含有スチレン系樹脂および成形品
JP3699579B2 (ja) * 1998-01-13 2005-09-28 積水化学工業株式会社 断熱層付き管継手およびその製造方法
JP2002194108A (ja) * 2000-12-26 2002-07-10 Tsutsunaka Plast Ind Co Ltd 加圧下で加熱積層されるａｂｓ系樹脂シートおよびその積層シートと製造方法。
JP2010116478A (ja) * 2008-11-13 2010-05-27 Shin Kobe Electric Mach Co Ltd 断熱パネル用熱可塑性樹脂シート及び断熱パネル
WO2016068303A1 (ja) * 2014-10-30 2016-05-06 旭ファイバーグラス株式会社 透明ａｂｓ樹脂組成物

Cited By (12)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
WO2020196318A1 (ja) * 2019-03-22 2020-10-01 積水化学工業株式会社 管継手及び配管構造
CN113614157A (zh) * 2019-03-22 2021-11-05 积水化学工业株式会社 管接头以及配管结构
JP2023040279A (ja) * 2019-03-22 2023-03-22 積水化学工業株式会社 管継手及び配管構造
US11840829B2 (en) 2019-03-22 2023-12-12 Sekisui Chemical Co., Ltd. Pipe joint and piping structure
CN113614157B (zh) * 2019-03-22 2024-01-09 积水化学工业株式会社 管接头以及配管结构
JP7596413B2 (ja) 2019-03-22 2024-12-09 積水化学工業株式会社 管継手及び配管構造並びに管継手の製造方法
JP2022048587A (ja) * 2020-09-15 2022-03-28 積水化学工業株式会社 管継手、配管構造、及び管継手の製造方法
JP7521983B2 (ja) 2020-09-15 2024-07-24 積水化学工業株式会社 管継手、配管構造、及び管継手の製造方法
JP2024128066A (ja) * 2020-09-15 2024-09-20 積水化学工業株式会社 管継手とその製造方法
JP7854011B2 (ja) 2020-09-15 2026-04-30 積水化学工業株式会社 管継手とその製造方法
JP2022052156A (ja) * 2020-09-23 2022-04-04 積水化学工業株式会社 管継手
JP7480005B2 (ja) 2020-09-23 2024-05-09 積水化学工業株式会社 管継手

Also Published As

Publication number Publication date
US11530309B2 (en) 2022-12-20
JP6581749B2 (ja) 2019-09-25
PH12020550129A1 (en) 2021-02-08
CN111315574A (zh) 2020-06-19
KR102567701B1 (ko) 2023-08-18
JP2020073809A (ja) 2020-05-14
JP2023089303A (ja) 2023-06-27
CN111315574B (zh) 2022-09-20
KR20200060379A (ko) 2020-05-29
JP7272903B2 (ja) 2023-05-12
JP7667813B2 (ja) 2025-04-23
SG11202002766WA (en) 2020-04-29
PH12020550129B1 (en) 2023-10-25
JPWO2019065834A1 (ja) 2019-11-14
US20210198443A1 (en) 2021-07-01
MY200401A (en) 2023-12-23

Similar Documents

Publication Publication Date Title
JP7667813B2 (ja) 発泡管継手及び配管構造
JP5498162B2 (ja) ポリプロピレン系樹脂発泡粒子及びその成型体
CN1317118C (zh) 多层泡沫材料
JP7277216B2 (ja) 継手構造
CA3023668C (en) Polymeric foam comprising low levels of brominated flame retardant and method of making same
CN105061880B (zh) 一种高光泽、高韧性冰箱内胆用合金材料及其制备方法
JP7596413B2 (ja) 管継手及び配管構造並びに管継手の製造方法
JP7184580B2 (ja) 伸縮継手及び伸縮配管構造
JP7854011B2 (ja) 管継手とその製造方法
JP2008144025A (ja) スチレン系樹脂発泡シートの製造方法
US20190203007A1 (en) High temperature non-crosslinked polyethylene-based foam and method of making the same
JP2021143731A (ja) 多層管
JP2015145503A (ja) 樹脂発泡体及び円筒体、成型体
JP2018172600A (ja) 発泡管継手およびその製造方法
JP4925290B2 (ja) ポリスチレン系樹脂積層発泡シート及びその成形品
JP2021127678A (ja) 断熱サッシ
JP2018173150A (ja) 樹脂管継手
JP2023003786A (ja) 樹脂組成物、発泡成形体及び多層管
JP2023147708A (ja) 樹脂多層管
JP2012131848A (ja) 樹脂発泡体及び円筒体、成型体

Legal Events

Date Code Title Description
ENP Entry into the national phase

Ref document number: 2019524297

Country of ref document: JP

Kind code of ref document: A

121 Ep: the epo has been informed by wipo that ep was designated in this application

Ref document number: 18861771

Country of ref document: EP

Kind code of ref document: A1

NENP Non-entry into the national phase

Ref country code: DE

122 Ep: pct application non-entry in european phase

Ref document number: 18861771

Country of ref document: EP

Kind code of ref document: A1