JP2020186806A - Heat-resistant transparent joint - Google Patents
Heat-resistant transparent joint Download PDFInfo
- Publication number
- JP2020186806A JP2020186806A JP2019093767A JP2019093767A JP2020186806A JP 2020186806 A JP2020186806 A JP 2020186806A JP 2019093767 A JP2019093767 A JP 2019093767A JP 2019093767 A JP2019093767 A JP 2019093767A JP 2020186806 A JP2020186806 A JP 2020186806A
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- JP
- Japan
- Prior art keywords
- heat
- resistant transparent
- vinyl chloride
- receiving portion
- joint
- 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.)
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- BZHJMEDXRYGGRV-UHFFFAOYSA-N Vinyl chloride Chemical compound ClC=C BZHJMEDXRYGGRV-UHFFFAOYSA-N 0.000 claims abstract description 45
- 229920005989 resin Polymers 0.000 claims abstract description 37
- 239000011347 resin Substances 0.000 claims abstract description 37
- 239000011342 resin composition Substances 0.000 claims abstract description 25
- ZAMOUSCENKQFHK-UHFFFAOYSA-N Chlorine atom Chemical compound [Cl] ZAMOUSCENKQFHK-UHFFFAOYSA-N 0.000 claims abstract description 14
- 239000000460 chlorine Substances 0.000 claims abstract description 14
- 229910052801 chlorine Inorganic materials 0.000 claims abstract description 14
- 239000003381 stabilizer Substances 0.000 claims description 28
- -1 octyl tin mercapto Chemical class 0.000 claims description 15
- ATJFFYVFTNAWJD-UHFFFAOYSA-N Tin Chemical compound [Sn] ATJFFYVFTNAWJD-UHFFFAOYSA-N 0.000 claims description 12
- 230000002093 peripheral effect Effects 0.000 claims description 5
- 238000000465 moulding Methods 0.000 abstract description 12
- 238000011156 evaluation Methods 0.000 description 15
- 238000002845 discoloration Methods 0.000 description 14
- 238000000034 method Methods 0.000 description 9
- 239000000178 monomer Substances 0.000 description 9
- 229920000642 polymer Polymers 0.000 description 7
- 239000004801 Chlorinated PVC Substances 0.000 description 6
- 229920000457 chlorinated polyvinyl chloride Polymers 0.000 description 6
- 235000014113 dietary fatty acids Nutrition 0.000 description 6
- 239000000194 fatty acid Substances 0.000 description 6
- 229930195729 fatty acid Natural products 0.000 description 6
- 238000005660 chlorination reaction Methods 0.000 description 5
- 229920001577 copolymer Polymers 0.000 description 5
- 239000011701 zinc Substances 0.000 description 5
- 150000004665 fatty acids Chemical class 0.000 description 4
- 238000001746 injection moulding Methods 0.000 description 4
- 229920005992 thermoplastic resin Polymers 0.000 description 4
- 239000000654 additive Substances 0.000 description 3
- 235000013351 cheese Nutrition 0.000 description 3
- HGQSXVKHVMGQRG-UHFFFAOYSA-N dioctyltin Chemical compound CCCCCCCC[Sn]CCCCCCCC HGQSXVKHVMGQRG-UHFFFAOYSA-N 0.000 description 3
- 229910052751 metal Inorganic materials 0.000 description 3
- 239000002184 metal Substances 0.000 description 3
- 238000006116 polymerization reaction Methods 0.000 description 3
- 239000004800 polyvinyl chloride Substances 0.000 description 3
- 229920000915 polyvinyl chloride Polymers 0.000 description 3
- 150000003839 salts Chemical class 0.000 description 3
- UZKWTJUDCOPSNM-UHFFFAOYSA-N 1-ethenoxybutane Chemical compound CCCCOC=C UZKWTJUDCOPSNM-UHFFFAOYSA-N 0.000 description 2
- GGSRTHRSSCWGGK-UHFFFAOYSA-L 2,2-dibutyl-5-hydroxy-1,3,2-dioxastannepane-4,7-dione Chemical compound CCCC[Sn]1(CCCC)OC(=O)CC(O)C(=O)O1 GGSRTHRSSCWGGK-UHFFFAOYSA-L 0.000 description 2
- NIXOWILDQLNWCW-UHFFFAOYSA-M Acrylate Chemical compound [O-]C(=O)C=C NIXOWILDQLNWCW-UHFFFAOYSA-M 0.000 description 2
- OYPRJOBELJOOCE-UHFFFAOYSA-N Calcium Chemical compound [Ca] OYPRJOBELJOOCE-UHFFFAOYSA-N 0.000 description 2
- LSDPWZHWYPCBBB-UHFFFAOYSA-N Methanethiol Chemical compound SC LSDPWZHWYPCBBB-UHFFFAOYSA-N 0.000 description 2
- 239000006057 Non-nutritive feed additive Substances 0.000 description 2
- 239000004698 Polyethylene Substances 0.000 description 2
- 239000004743 Polypropylene Substances 0.000 description 2
- PPBRXRYQALVLMV-UHFFFAOYSA-N Styrene Chemical compound C=CC1=CC=CC=C1 PPBRXRYQALVLMV-UHFFFAOYSA-N 0.000 description 2
- QYKIQEUNHZKYBP-UHFFFAOYSA-N Vinyl ether Chemical class C=COC=C QYKIQEUNHZKYBP-UHFFFAOYSA-N 0.000 description 2
- HCHKCACWOHOZIP-UHFFFAOYSA-N Zinc Chemical compound [Zn] HCHKCACWOHOZIP-UHFFFAOYSA-N 0.000 description 2
- WPYMKLBDIGXBTP-UHFFFAOYSA-N benzoic acid Chemical compound OC(=O)C1=CC=CC=C1 WPYMKLBDIGXBTP-UHFFFAOYSA-N 0.000 description 2
- 229910052793 cadmium Inorganic materials 0.000 description 2
- 229910052791 calcium Inorganic materials 0.000 description 2
- 239000011575 calcium Substances 0.000 description 2
- 239000003795 chemical substances by application Substances 0.000 description 2
- 239000003086 colorant Substances 0.000 description 2
- 230000000052 comparative effect Effects 0.000 description 2
- UKMSUNONTOPOIO-UHFFFAOYSA-N docosanoic acid Chemical compound CCCCCCCCCCCCCCCCCCCCCC(O)=O UKMSUNONTOPOIO-UHFFFAOYSA-N 0.000 description 2
- POULHZVOKOAJMA-UHFFFAOYSA-N dodecanoic acid Chemical compound CCCCCCCCCCCC(O)=O POULHZVOKOAJMA-UHFFFAOYSA-N 0.000 description 2
- 229920006244 ethylene-ethyl acrylate Polymers 0.000 description 2
- 238000010438 heat treatment Methods 0.000 description 2
- IPCSVZSSVZVIGE-UHFFFAOYSA-N hexadecanoic acid Chemical compound CCCCCCCCCCCCCCCC(O)=O IPCSVZSSVZVIGE-UHFFFAOYSA-N 0.000 description 2
- 239000000314 lubricant Substances 0.000 description 2
- HQKMJHAJHXVSDF-UHFFFAOYSA-L magnesium stearate Chemical compound [Mg+2].CCCCCCCCCCCCCCCCCC([O-])=O.CCCCCCCCCCCCCCCCCC([O-])=O HQKMJHAJHXVSDF-UHFFFAOYSA-L 0.000 description 2
- 229940049920 malate Drugs 0.000 description 2
- BJEPYKJPYRNKOW-UHFFFAOYSA-L malate(2-) Chemical compound [O-]C(=O)C(O)CC([O-])=O BJEPYKJPYRNKOW-UHFFFAOYSA-L 0.000 description 2
- 239000000203 mixture Substances 0.000 description 2
- 239000003607 modifier Substances 0.000 description 2
- 210000002445 nipple Anatomy 0.000 description 2
- QIQXTHQIDYTFRH-UHFFFAOYSA-N octadecanoic acid Chemical compound CCCCCCCCCCCCCCCCCC(O)=O QIQXTHQIDYTFRH-UHFFFAOYSA-N 0.000 description 2
- 229920000573 polyethylene Polymers 0.000 description 2
- 229920001155 polypropylene Polymers 0.000 description 2
- 238000005979 thermal decomposition reaction Methods 0.000 description 2
- 238000004448 titration Methods 0.000 description 2
- 239000012780 transparent material Substances 0.000 description 2
- 229920002554 vinyl polymer Polymers 0.000 description 2
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 2
- 229910052725 zinc Inorganic materials 0.000 description 2
- WRIDQFICGBMAFQ-UHFFFAOYSA-N (E)-8-Octadecenoic acid Natural products CCCCCCCCCC=CCCCCCCC(O)=O WRIDQFICGBMAFQ-UHFFFAOYSA-N 0.000 description 1
- HIDBROSJWZYGSZ-UHFFFAOYSA-N 1-phenylpyrrole-2,5-dione Chemical compound O=C1C=CC(=O)N1C1=CC=CC=C1 HIDBROSJWZYGSZ-UHFFFAOYSA-N 0.000 description 1
- LQJBNNIYVWPHFW-UHFFFAOYSA-N 20:1omega9c fatty acid Natural products CCCCCCCCCCC=CCCCCCCCC(O)=O LQJBNNIYVWPHFW-UHFFFAOYSA-N 0.000 description 1
- UJTRCPVECIHPBG-UHFFFAOYSA-N 3-cyclohexylpyrrole-2,5-dione Chemical compound O=C1NC(=O)C(C2CCCCC2)=C1 UJTRCPVECIHPBG-UHFFFAOYSA-N 0.000 description 1
- UKWUOTZGXIZAJC-UHFFFAOYSA-N 4-nitrosalicylic acid Chemical compound OC(=O)C1=CC=C([N+]([O-])=O)C=C1O UKWUOTZGXIZAJC-UHFFFAOYSA-N 0.000 description 1
- QSBYPNXLFMSGKH-UHFFFAOYSA-N 9-Heptadecensaeure Natural products CCCCCCCC=CCCCCCCCC(O)=O QSBYPNXLFMSGKH-UHFFFAOYSA-N 0.000 description 1
- 229920000178 Acrylic resin Polymers 0.000 description 1
- 239000004925 Acrylic resin Substances 0.000 description 1
- 235000021357 Behenic acid Nutrition 0.000 description 1
- 239000005711 Benzoic acid Substances 0.000 description 1
- VDHUYCCCYAYPJS-UHFFFAOYSA-H C(CCCCCCCCCCC)(=O)[O-].S[Sn+](CCCC)CCCC.[Sn+4].C(CCCCCCCCCCC)(=O)[O-].C(CCCCCCCCCCC)(=O)[O-].C(CCCCCCCCCCC)(=O)[O-].C(CCCCCCCCCCC)(=O)[O-] Chemical compound C(CCCCCCCCCCC)(=O)[O-].S[Sn+](CCCC)CCCC.[Sn+4].C(CCCCCCCCCCC)(=O)[O-].C(CCCCCCCCCCC)(=O)[O-].C(CCCCCCCCCCC)(=O)[O-].C(CCCCCCCCCCC)(=O)[O-] VDHUYCCCYAYPJS-UHFFFAOYSA-H 0.000 description 1
- 239000004709 Chlorinated polyethylene Substances 0.000 description 1
- 239000004609 Impact Modifier Substances 0.000 description 1
- 239000005639 Lauric acid Substances 0.000 description 1
- 240000002129 Malva sylvestris Species 0.000 description 1
- 235000006770 Malva sylvestris Nutrition 0.000 description 1
- CERQOIWHTDAKMF-UHFFFAOYSA-N Methacrylic acid Chemical class CC(=C)C(O)=O CERQOIWHTDAKMF-UHFFFAOYSA-N 0.000 description 1
- 239000005642 Oleic acid Substances 0.000 description 1
- ZQPPMHVWECSIRJ-UHFFFAOYSA-N Oleic acid Natural products CCCCCCCCC=CCCCCCCCC(O)=O ZQPPMHVWECSIRJ-UHFFFAOYSA-N 0.000 description 1
- 235000021314 Palmitic acid Nutrition 0.000 description 1
- 239000002202 Polyethylene glycol Substances 0.000 description 1
- 239000004793 Polystyrene Substances 0.000 description 1
- 235000021355 Stearic acid Nutrition 0.000 description 1
- 244000269722 Thea sinensis Species 0.000 description 1
- XTXRWKRVRITETP-UHFFFAOYSA-N Vinyl acetate Chemical compound CC(=O)OC=C XTXRWKRVRITETP-UHFFFAOYSA-N 0.000 description 1
- UKLDJPRMSDWDSL-UHFFFAOYSA-L [dibutyl(dodecanoyloxy)stannyl] dodecanoate Chemical compound CCCCCCCCCCCC(=O)O[Sn](CCCC)(CCCC)OC(=O)CCCCCCCCCCC UKLDJPRMSDWDSL-UHFFFAOYSA-L 0.000 description 1
- 239000006096 absorbing agent Substances 0.000 description 1
- 229920000122 acrylonitrile butadiene styrene Polymers 0.000 description 1
- 230000000996 additive effect Effects 0.000 description 1
- XYLMUPLGERFSHI-UHFFFAOYSA-N alpha-Methylstyrene Chemical compound CC(=C)C1=CC=CC=C1 XYLMUPLGERFSHI-UHFFFAOYSA-N 0.000 description 1
- 239000003963 antioxidant agent Substances 0.000 description 1
- 230000003078 antioxidant effect Effects 0.000 description 1
- 229910052788 barium Inorganic materials 0.000 description 1
- DSAJWYNOEDNPEQ-UHFFFAOYSA-N barium atom Chemical compound [Ba] DSAJWYNOEDNPEQ-UHFFFAOYSA-N 0.000 description 1
- AGXUVMPSUKZYDT-UHFFFAOYSA-L barium(2+);octadecanoate Chemical compound [Ba+2].CCCCCCCCCCCCCCCCCC([O-])=O.CCCCCCCCCCCCCCCCCC([O-])=O AGXUVMPSUKZYDT-UHFFFAOYSA-L 0.000 description 1
- 229940116226 behenic acid Drugs 0.000 description 1
- 235000010233 benzoic acid Nutrition 0.000 description 1
- CQEYYJKEWSMYFG-UHFFFAOYSA-N butyl acrylate Chemical compound CCCCOC(=O)C=C CQEYYJKEWSMYFG-UHFFFAOYSA-N 0.000 description 1
- BDOSMKKIYDKNTQ-UHFFFAOYSA-N cadmium atom Chemical compound [Cd] BDOSMKKIYDKNTQ-UHFFFAOYSA-N 0.000 description 1
- GWOWVOYJLHSRJJ-UHFFFAOYSA-L cadmium stearate Chemical compound [Cd+2].CCCCCCCCCCCCCCCCCC([O-])=O.CCCCCCCCCCCCCCCCCC([O-])=O GWOWVOYJLHSRJJ-UHFFFAOYSA-L 0.000 description 1
- RXROCZREIWVERD-UHFFFAOYSA-L cadmium(2+);2-ethylhexanoate Chemical compound [Cd+2].CCCCC(CC)C([O-])=O.CCCCC(CC)C([O-])=O RXROCZREIWVERD-UHFFFAOYSA-L 0.000 description 1
- ITQVEYJXZXMBTR-UHFFFAOYSA-L cadmium(2+);dodecanoate Chemical compound [Cd+2].CCCCCCCCCCCC([O-])=O.CCCCCCCCCCCC([O-])=O ITQVEYJXZXMBTR-UHFFFAOYSA-L 0.000 description 1
- CJZGTCYPCWQAJB-UHFFFAOYSA-L calcium stearate Chemical compound [Ca+2].CCCCCCCCCCCCCCCCCC([O-])=O.CCCCCCCCCCCCCCCCCC([O-])=O CJZGTCYPCWQAJB-UHFFFAOYSA-L 0.000 description 1
- 239000008116 calcium stearate Substances 0.000 description 1
- 235000013539 calcium stearate Nutrition 0.000 description 1
- HIAAVKYLDRCDFQ-UHFFFAOYSA-L calcium;dodecanoate Chemical compound [Ca+2].CCCCCCCCCCCC([O-])=O.CCCCCCCCCCCC([O-])=O HIAAVKYLDRCDFQ-UHFFFAOYSA-L 0.000 description 1
- 229910002090 carbon oxide Inorganic materials 0.000 description 1
- 150000007942 carboxylates Chemical class 0.000 description 1
- 239000003638 chemical reducing agent Substances 0.000 description 1
- 238000013329 compounding Methods 0.000 description 1
- 150000001875 compounds Chemical class 0.000 description 1
- 238000001816 cooling Methods 0.000 description 1
- 238000004132 cross linking Methods 0.000 description 1
- 239000003431 cross linking reagent Substances 0.000 description 1
- UQLDLKMNUJERMK-UHFFFAOYSA-L di(octadecanoyloxy)lead Chemical compound [Pb+2].CCCCCCCCCCCCCCCCCC([O-])=O.CCCCCCCCCCCCCCCCCC([O-])=O UQLDLKMNUJERMK-UHFFFAOYSA-L 0.000 description 1
- AYOHIQLKSOJJQH-UHFFFAOYSA-N dibutyltin Chemical compound CCCC[Sn]CCCC AYOHIQLKSOJJQH-UHFFFAOYSA-N 0.000 description 1
- 230000000694 effects Effects 0.000 description 1
- 238000010894 electron beam technology Methods 0.000 description 1
- 230000002708 enhancing effect Effects 0.000 description 1
- UIWXSTHGICQLQT-UHFFFAOYSA-N ethenyl propanoate Chemical compound CCC(=O)OC=C UIWXSTHGICQLQT-UHFFFAOYSA-N 0.000 description 1
- 125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 description 1
- 239000005038 ethylene vinyl acetate Substances 0.000 description 1
- 229920005680 ethylene-methyl methacrylate copolymer Polymers 0.000 description 1
- 238000005227 gel permeation chromatography Methods 0.000 description 1
- 229920000578 graft copolymer Polymers 0.000 description 1
- 229920001519 homopolymer Polymers 0.000 description 1
- 230000001771 impaired effect Effects 0.000 description 1
- 239000012796 inorganic flame retardant Substances 0.000 description 1
- 230000001678 irradiating effect Effects 0.000 description 1
- QXJSBBXBKPUZAA-UHFFFAOYSA-N isooleic acid Natural products CCCCCCCC=CCCCCCCCCC(O)=O QXJSBBXBKPUZAA-UHFFFAOYSA-N 0.000 description 1
- 239000010410 layer Substances 0.000 description 1
- GIWKOZXJDKMGQC-UHFFFAOYSA-L lead(2+);naphthalene-2-carboxylate Chemical compound [Pb+2].C1=CC=CC2=CC(C(=O)[O-])=CC=C21.C1=CC=CC2=CC(C(=O)[O-])=CC=C21 GIWKOZXJDKMGQC-UHFFFAOYSA-L 0.000 description 1
- 239000004611 light stabiliser Substances 0.000 description 1
- HGPXWXLYXNVULB-UHFFFAOYSA-M lithium stearate Chemical compound [Li+].CCCCCCCCCCCCCCCCCC([O-])=O HGPXWXLYXNVULB-UHFFFAOYSA-M 0.000 description 1
- 235000019359 magnesium stearate Nutrition 0.000 description 1
- 150000004701 malic acid derivatives Chemical class 0.000 description 1
- 238000004519 manufacturing process Methods 0.000 description 1
- 239000000463 material Substances 0.000 description 1
- 238000005259 measurement Methods 0.000 description 1
- 238000002844 melting Methods 0.000 description 1
- 230000008018 melting Effects 0.000 description 1
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 description 1
- 238000002156 mixing Methods 0.000 description 1
- 238000012986 modification Methods 0.000 description 1
- 230000004048 modification Effects 0.000 description 1
- WQEPLUUGTLDZJY-UHFFFAOYSA-N n-Pentadecanoic acid Natural products CCCCCCCCCCCCCCC(O)=O WQEPLUUGTLDZJY-UHFFFAOYSA-N 0.000 description 1
- OQCDKBAXFALNLD-UHFFFAOYSA-N octadecanoic acid Natural products CCCCCCCC(C)CCCCCCCCC(O)=O OQCDKBAXFALNLD-UHFFFAOYSA-N 0.000 description 1
- ZQPPMHVWECSIRJ-KTKRTIGZSA-N oleic acid Chemical compound CCCCCCCC\C=C/CCCCCCCC(O)=O ZQPPMHVWECSIRJ-KTKRTIGZSA-N 0.000 description 1
- 125000000913 palmityl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 description 1
- 150000002978 peroxides Chemical class 0.000 description 1
- 239000004014 plasticizer Substances 0.000 description 1
- 229920001200 poly(ethylene-vinyl acetate) Polymers 0.000 description 1
- 229920001083 polybutene Polymers 0.000 description 1
- 229920001223 polyethylene glycol Polymers 0.000 description 1
- 229920000139 polyethylene terephthalate Polymers 0.000 description 1
- 239000005020 polyethylene terephthalate Substances 0.000 description 1
- 229920002223 polystyrene Polymers 0.000 description 1
- 229920002635 polyurethane Polymers 0.000 description 1
- 239000004814 polyurethane Substances 0.000 description 1
- WBHHMMIMDMUBKC-XLNAKTSKSA-N ricinelaidic acid Chemical compound CCCCCC[C@@H](O)C\C=C\CCCCCCCC(O)=O WBHHMMIMDMUBKC-XLNAKTSKSA-N 0.000 description 1
- 229960003656 ricinoleic acid Drugs 0.000 description 1
- FEUQNCSVHBHROZ-UHFFFAOYSA-N ricinoleic acid Natural products CCCCCCC(O[Si](C)(C)C)CC=CCCCCCCCC(=O)OC FEUQNCSVHBHROZ-UHFFFAOYSA-N 0.000 description 1
- 239000002356 single layer Substances 0.000 description 1
- 230000006641 stabilisation Effects 0.000 description 1
- 238000011105 stabilization Methods 0.000 description 1
- 239000008117 stearic acid Substances 0.000 description 1
- 238000003756 stirring Methods 0.000 description 1
- FRKHZXHEZFADLA-UHFFFAOYSA-L strontium;octadecanoate Chemical compound [Sr+2].CCCCCCCCCCCCCCCCCC([O-])=O.CCCCCCCCCCCCCCCCCC([O-])=O FRKHZXHEZFADLA-UHFFFAOYSA-L 0.000 description 1
- 239000000126 substance Substances 0.000 description 1
- 238000012360 testing method Methods 0.000 description 1
- 125000000383 tetramethylene group Chemical group [H]C([H])([*:1])C([H])([H])C([H])([H])C([H])([H])[*:2] 0.000 description 1
- 229920001169 thermoplastic Polymers 0.000 description 1
- 229920002725 thermoplastic elastomer Polymers 0.000 description 1
- 239000004416 thermosoftening plastic Substances 0.000 description 1
- 125000003396 thiol group Chemical group [H]S* 0.000 description 1
- 229920001567 vinyl ester resin Polymers 0.000 description 1
- 125000000391 vinyl group Chemical group [H]C([*])=C([H])[H] 0.000 description 1
- 229940098697 zinc laurate Drugs 0.000 description 1
- XOOUIPVCVHRTMJ-UHFFFAOYSA-L zinc stearate Chemical compound [Zn+2].CCCCCCCCCCCCCCCCCC([O-])=O.CCCCCCCCCCCCCCCCCC([O-])=O XOOUIPVCVHRTMJ-UHFFFAOYSA-L 0.000 description 1
- IFNXAMCERSVZCV-UHFFFAOYSA-L zinc;2-ethylhexanoate Chemical compound [Zn+2].CCCCC(CC)C([O-])=O.CCCCC(CC)C([O-])=O IFNXAMCERSVZCV-UHFFFAOYSA-L 0.000 description 1
- GPYYEEJOMCKTPR-UHFFFAOYSA-L zinc;dodecanoate Chemical compound [Zn+2].CCCCCCCCCCCC([O-])=O.CCCCCCCCCCCC([O-])=O GPYYEEJOMCKTPR-UHFFFAOYSA-L 0.000 description 1
- 239000004711 α-olefin Substances 0.000 description 1
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Abstract
Description
本発明は耐熱透明継手に関する。 The present invention relates to a heat resistant transparent joint.
給湯用途にて用いられている耐熱性硬質塩化ビニル樹脂を継手に採用した排水専用継手と、耐熱パイプとを組み合わせた配管システムが、厨房排水や食洗器、電気温水器等から流される高温排水に用いられている(例えば、非特許文献1参照)。 A piping system that combines a heat-resistant pipe and a drainage joint that uses heat-resistant rigid vinyl chloride resin used for hot water supply is a high-temperature drainage that flows from kitchen drainage, dishwashers, electric water heaters, etc. (See, for example, Non-Patent Document 1).
呼び径が75以上である大口径の耐熱透明継手の成形時には、継手が黄色く変色するヤケと呼ばれる現象が生じる場合がある。
しかし、従来、ヤケを低減する措置は十分に講じられてこなかった。
When forming a large-diameter heat-resistant transparent joint having a nominal diameter of 75 or more, a phenomenon called discoloration may occur in which the joint turns yellow.
However, in the past, measures to reduce discoloration have not been sufficiently taken.
そこで、本発明は、成形時に生じるヤケが低減された大口径の耐熱透明継手を提供することを課題とする。 Therefore, an object of the present invention is to provide a large-diameter heat-resistant transparent joint in which discoloration generated during molding is reduced.
上記課題は、以下の構成によって解決される。
[1] 内部に流路を有し、2以上の開口部が形成された本体部と、前記本体部の開口部の周縁を囲む受入部とを備え、
前記本体部及び前記受入部は、塩化ビニル系樹脂を含む、塩素含有量が56.6〜58.2質量%である樹脂組成物からなり、
前記受入部のうち少なくとも1つは、呼び径が75〜100である管の端部を差込み可能である、耐熱透明継手。
[2] 前記樹脂組成物が錫系安定剤を含む、[1]に記載の耐熱透明継手。
[3] 前記錫系安定剤の含有量が前記塩化ビニル系樹脂100質量部に対して4.0〜10.0質量部である、[2]に記載の耐熱透明継手。
[4] 前記錫系安定剤がオクチル錫メルカプト安定剤である、[2]又は[3]に記載の耐熱透明継手。
The above problem is solved by the following configuration.
[1] A main body having a flow path inside and having two or more openings formed therein, and a receiving portion surrounding the peripheral edge of the opening of the main body are provided.
The main body portion and the receiving portion are made of a resin composition containing a vinyl chloride resin and having a chlorine content of 56.6 to 58.2% by mass.
At least one of the receiving portions is a heat-resistant transparent joint into which an end portion of a pipe having a nominal diameter of 75 to 100 can be inserted.
[2] The heat-resistant transparent joint according to [1], wherein the resin composition contains a tin-based stabilizer.
[3] The heat-resistant transparent joint according to [2], wherein the content of the tin-based stabilizer is 4.0 to 10.0 parts by mass with respect to 100 parts by mass of the vinyl chloride-based resin.
[4] The heat-resistant transparent joint according to [2] or [3], wherein the tin-based stabilizer is an octyl tin mercapto stabilizer.
本発明によれば、成形時に生じるヤケが低減された大口径の耐熱透明継手を提供できる。 According to the present invention, it is possible to provide a heat-resistant transparent joint having a large diameter with reduced discoloration generated during molding.
本明細書において、「〜」を用いて表される数値範囲は、その両端の数値を含むものとする。
本明細書において、「透明」とは、肉眼で、継手の外側から継手の内部を視認できることをいう。より具体的には、JIS K 7136:2000「プラスチック−透明材料のヘーズの求め方」に従って測定したヘイズ値が20〜80であることをいう。
In the present specification, the numerical range represented by using "~" shall include the numerical values at both ends thereof.
In the present specification, "transparent" means that the inside of the joint can be visually recognized from the outside of the joint with the naked eye. More specifically, it means that the haze value measured according to JIS K 7136: 2000 "How to determine the haze of a plastic-transparent material" is 20 to 80.
[耐熱透明継手]
本発明の耐熱透明継手は、内部に流路を有し、2以上の開口部が形成された本体部と、前記本体部の開口部の周縁を囲む受入部とを備え
前記本体部及び前記受入部は、塩化ビニル系樹脂を含む、塩素含有量が56.6〜58.2質量%である樹脂組成物からなる。
前記受入部のうち少なくとも1つは、呼び径が75〜100である管の端部を差込み可能である。
[Heat-resistant transparent fitting]
The heat-resistant transparent joint of the present invention includes a main body portion having a flow path inside and having two or more openings formed therein, and a receiving portion surrounding the peripheral edge of the opening of the main body portion, and the main body portion and the receiving portion. The part comprises a resin composition containing a vinyl chloride resin and having a chlorine content of 56.6 to 58.2% by mass.
At least one of the receiving portions is capable of inserting the end portion of a pipe having a nominal diameter of 75 to 100.
<第一の実施形態>
以下、本発明の耐熱透明継手の第一の実施形態について、図1及び図2を参照しながら説明する。
図1は、本発明の耐熱透明継手の第一の実施形態を示す側面図であり、図2は、図1に示す耐熱透明継手の縦断面図である。
図1及び図2に示すように、本発明の第一の実施形態に係る耐熱透明継手1は、ドレンパイプの接続に使用されるエルボを一例としている。耐熱透明継手1は、内部に屈曲する流路14を有し、両端に第1の開口部12aと第2の開口部12bとを有する本体部10を備える。耐熱透明継手1は、本体部10の第1の開口部12aの周縁を囲む円筒状の第1の受入部11aと、本体部10の第2の開口部12bの周縁を囲む円筒状の第2の受入部11bとを備える。本体部10と、第1の受入部11aと、第2の受入部11bとは、一体に形成されている。
<First Embodiment>
Hereinafter, the first embodiment of the heat-resistant transparent joint of the present invention will be described with reference to FIGS. 1 and 2.
FIG. 1 is a side view showing a first embodiment of the heat-resistant transparent joint of the present invention, and FIG. 2 is a vertical cross-sectional view of the heat-resistant transparent joint shown in FIG.
As shown in FIGS. 1 and 2, the heat-resistant transparent joint 1 according to the first embodiment of the present invention uses an elbow used for connecting a drain pipe as an example. The heat-resistant transparent joint 1 includes a
受入部11には、受入部11の内径とほぼ同外径の管部材が挿入される。受入部11の少なくとも1つは、呼び径が75〜100である管の端部を差込み可能である。受入部の開口部13の内径は、本体部10の開口部12の内径よりも大きい。
A pipe member having a diameter substantially the same as the inner diameter of the
管を挿入した際の視認性を向上させる観点から、受入部11の厚さは均一であることが好ましい。
受入部11の厚さは、特に限定されないが、例えば、2〜8mmが好ましく、3〜5mmがより好ましい。受入部11の厚さがこの範囲内であると、受入部11の強度を維持しやすく、かつ、受入部11の視認性を向上しやすい。
本体部10の厚さは、特に限定されないが、例えば、2〜8mmが好ましく、3〜6mmがより好ましい。本体部10の厚さがこの範囲内であると、本体部10の強度を維持しやすく、かつ、耐熱透明継手1の軽量化を図りやすい。
From the viewpoint of improving visibility when the tube is inserted, it is preferable that the
The thickness of the
The thickness of the
図1及び図2において、Yは、耐熱透明継手1を射出成形する際に用いられる射出成形用金型のキャビティ内(空間)に樹脂組成物を導入するゲートの位置を示し、耐熱透明継手1にはゲートに対応する位置にゲート痕が形成される。
ゲート位置を本体部10のYとした場合、ゲートから受入部11までの距離が等しく、より受入部11のばらつきを小さくできる。Yは第1の受入部11a、第2の受入部11bからの距離が等しくなる位置であれば本体部10のどこにあってもよい。
In FIGS. 1 and 2, Y indicates the position of the gate for introducing the resin composition into the cavity (space) of the injection molding die used when the heat-resistant transparent joint 1 is injection-molded. A gate mark is formed at a position corresponding to the gate.
When the gate position is Y of the
<第二の実施形態>
以下、本発明の耐熱透明継手の第二の実施形態について、図3及び図4を参照しながら説明する。
図3は、本発明の耐熱透明継手の第二の実施形態を示す側面図であり、図4は、図3に示す耐熱透明継手の縦断面図である。
図3及び図4に示すように、本発明の第二の実施形態に係る耐熱透明継手2は、ドレンパイプの接続に使用されるチーズを一例としている。耐熱透明継手2は、内部に分岐又は合流する流路24を有し、端部に第1の開口部22aと、第2の開口部22bと、第3の開口部22cとを有する本体部20を備える。耐熱透明継手2は、本体部20の第1の開口部22aの辺縁を囲む円筒状の第1の受入部21aと、本体部20の第2の開口部22bの辺縁を囲む円筒状の第2の受入部21bと、本体部20の第3の開口部22cの辺縁を囲む円筒状の第3の受入部21cとを備える。本体部20と、第1の受入部21aと、第2の受入部21bと、第3の受入部21cとは、一体に形成されている。
受入部21には、受入部21の内径とほぼ同外径の管部材が挿入される。受入部21のうち1つ以上は、呼び径が75〜100である管の端部を差込み可能である。受入部の開口部23の内径は、本体部20の開口部22の内径よりも大きい。
<Second embodiment>
Hereinafter, a second embodiment of the heat-resistant transparent joint of the present invention will be described with reference to FIGS. 3 and 4.
FIG. 3 is a side view showing a second embodiment of the heat-resistant transparent joint of the present invention, and FIG. 4 is a vertical sectional view of the heat-resistant transparent joint shown in FIG.
As shown in FIGS. 3 and 4, the heat-resistant
A pipe member having a diameter substantially the same as the inner diameter of the
本体部20の3つの開口部22のうち、2つは第1の管軸O1と同軸の円形である。
また、3つの受入部21のうち、2つは第1の管軸O1と同軸の管状である。第1の管軸O1の一端側の受入部は第1の受入部21aであり、他端側の受入部は第2の受入部21bである。残りの1つは第2の管軸O2と同軸の管状であり、第3の受入部21cである。
Of the three
Further, two of the three receiving
管を挿入した際の視認性を向上させる観点から、受入部21の厚さは均一であることが好ましい。
受入部21の厚さは、特に限定されないが、例えば、2〜8mmが好ましく、3〜5mmがより好ましい。受入部21の厚さがこの範囲内であると、受入部21の強度を維持しやすく、かつ、受入部21の視認性を向上しやすい。
本体部20の厚さは、特に限定されないが、例えば、2〜8mmが好ましく、3〜6mmがより好ましい。本体部20の厚さがこの範囲内であると、本体部20の強度を維持しやすく、かつ、耐熱透明継手2の軽量化を図りやすい。
From the viewpoint of improving visibility when the tube is inserted, it is preferable that the
The thickness of the
The thickness of the
図3及び図4において、Yは、耐熱透明継手2を射出成形する際に用いられる射出成形用金型のキャビティ内(空間)に樹脂組成物を導入するゲートの位置を示し、耐熱透明継手2にはゲートに対応する位置にゲート痕が形成される。
ゲート位置を本体部20のYとした場合、ゲートから受入部21までの距離が等しく、より受入部21のばらつきを小さくできる。なお、Yの位置は例示であって、Yは第1の受入部21a、第2の受入部21b、第3の受入部21cからの距離が等しくなる位置であれば本体部20のどこにあってもよい。
In FIGS. 3 and 4, Y indicates the position of the gate for introducing the resin composition into the cavity (space) of the injection molding die used when the heat-resistant transparent joint 2 is injection-molded. A gate mark is formed at a position corresponding to the gate.
When the gate position is Y of the
<樹脂組成物>
耐熱透明継手1(2)の本体部10(20)及び受入部11(21)は、塩化ビニル系樹脂を含み、塩素含有量が56.6〜58.2質量%である樹脂組成物からなる。
耐熱透明継手1(2)は、耐熱透明継手1(2)の全体が樹脂組成物からなる単層構造でもよいし、複数の層からなる積層構造でもよい。
<Resin composition>
The main body portion 10 (20) and the receiving portion 11 (21) of the heat-resistant transparent joint 1 (2) are made of a resin composition containing a vinyl chloride resin and having a chlorine content of 56.6 to 58.2% by mass. ..
The heat-resistant transparent joint 1 (2) may have a single-layer structure in which the entire heat-resistant transparent joint 1 (2) is made of a resin composition, or may be a laminated structure made of a plurality of layers.
樹脂組成物に含まれる塩化ビニル系樹脂としては、例えば、塩化ビニルモノマーの単独重合体;塩化ビニルモノマーと、該塩化ビニルモノマーと共重合可能な不飽和結合を有する他のモノマーとの共重合体;塩化ビニル系樹脂以外の重合体に塩化ビニルモノマーをグラフト共重合したグラフト共重合体等が挙げられる。
前記塩化ビニル系樹脂はさらに塩素化されてもよい。塩化ビニル系樹脂の塩素化方法としては、例えば、熱塩素化方法、光塩素化方法等が挙げられる。
Examples of the vinyl chloride resin contained in the resin composition include a homopolymer of a vinyl chloride monomer; a copolymer of a vinyl chloride monomer and another monomer having an unsaturated bond copolymerizable with the vinyl chloride monomer. Examples thereof include a graft copolymer obtained by graft-copolymerizing a vinyl chloride monomer with a polymer other than a vinyl chloride resin.
The vinyl chloride resin may be further chlorinated. Examples of the chlorination method for the vinyl chloride resin include a thermal chlorination method and a photochlorination method.
前記塩化ビニルモノマーと共重合可能な不飽和結合を有する他のモノマーとしては、例えば、エチレン、プロピレン、ブチレン等のα−オレフィン類;酢酸ビニル、プロピオン酸ビニル等のビニルエステル類;ブチルビニルエーテル、セチルビニルエーテル等のビニルエーテル類;メチル(メタ)アクリレート、エチル(メタ)アクリレート、ブチルアクリレート等の(メタ)アクリル酸エステル類;スチレン、α−メチルスチレン等の芳香族ビニル類;N−フェニルマレイミド、N−シクロヘキシルマレイミド等のN−置換マレイミド類等が挙げられる。前記他のモノマーは、1種を単独で使用してもよいし、2種以上を併用してもよい。 Examples of other monomers having an unsaturated bond copolymerizable with the vinyl chloride monomer include α-olefins such as ethylene, propylene and butylene; vinyl esters such as vinyl acetate and vinyl propionate; butyl vinyl ether and cetyl. Vinyl ethers such as vinyl ethers; (meth) acrylic acid esters such as methyl (meth) acrylate, ethyl (meth) acrylate and butyl acrylate; aromatic vinyls such as styrene and α-methylstyrene; N-phenylmaleimide, N- Examples thereof include N-substituted maleimides such as cyclohexyl maleimide. As the other monomer, one type may be used alone, or two or more types may be used in combination.
前記塩化ビニルモノマーをグラフト共重合する重合体としては、例えば、エチレン−酢酸ビニル共重合体、エチレン−酢酸ビニル−一酸化炭素共重合体、エチレン−エチルアクリレート共重合体、エチレン−ブチルアクリレート−一酸化炭素共重合体、エチレン−メチルメタクリレート共重合体、エチレン−プロピレン共重合体、アクリロニトリル−ブタジエン共重合体、ポリウレタン、塩素化ポリエチレン、塩素化ポリプロピレン等が挙げられる。これらの重合体は、1種を単独で使用してもよいし、2種以上を併用してもよい。 Examples of the polymer for graft-copolymerizing the vinyl chloride monomer include ethylene-vinyl acetate copolymer, ethylene-vinyl acetate-carbon monoxide copolymer, ethylene-ethyl acrylate copolymer, and ethylene-butyl acrylate-1. Examples thereof include carbon oxide copolymers, ethylene-methylmethacrylate copolymers, ethylene-propylene copolymers, acrylonitrile-butadiene copolymers, polyurethanes, chlorinated polyethylenes and chlorinated polypropylenes. One of these polymers may be used alone, or two or more of these polymers may be used in combination.
前記塩化ビニル系樹脂は架橋されていてもよい。塩化ビニル系樹脂の架橋方法としては、例えば、架橋剤及び過酸化物を添加する方法、電子線を照射する方法、水架橋性材料を使用する方法等が挙げられる。 The vinyl chloride resin may be crosslinked. Examples of the method for cross-linking the vinyl chloride resin include a method of adding a cross-linking agent and a peroxide, a method of irradiating an electron beam, and a method of using a water-crosslinkable material.
塩化ビニル系樹脂は、1種を単独で使用してもよいし、2種以上を併用してもよい。 As the vinyl chloride resin, one type may be used alone, or two or more types may be used in combination.
塩化ビニル系樹脂の質量平均分子量は、37500〜70000が好ましく、37500〜44000がより好ましい。
質量平均分子量は、ポリエチレングリコールを標準物質とするゲルパーミエーションクロマトグラフィーによる測定値である。
塩化ビニル系樹脂の質量平均分子量がこの範囲内であると、機械的強度をより高めることができ、かつ、十分な成形性を確保できる。
The mass average molecular weight of the vinyl chloride resin is preferably 37500 to 70000, more preferably 37500 to 44000.
The mass average molecular weight is a value measured by gel permeation chromatography using polyethylene glycol as a standard substance.
When the mass average molecular weight of the vinyl chloride resin is within this range, the mechanical strength can be further increased and sufficient moldability can be ensured.
塩化ビニル系樹脂がポリ塩化ビニルの場合、ポリ塩化ビニルの重合度は600〜800が好ましく、600〜700がより好ましい。
平均重合度は、質量平均分子量をクロロエチレンの分子量で除することにより算出できる。
ポリ塩化ビニルの平均重合度がこの範囲内であると、機械的強度をより高めることができ、かつ、十分な成形性を確保できる。
When the vinyl chloride resin is polyvinyl chloride, the degree of polymerization of polyvinyl chloride is preferably 600 to 800, more preferably 600 to 700.
The average degree of polymerization can be calculated by dividing the mass average molecular weight by the molecular weight of chloroethylene.
When the average degree of polymerization of polyvinyl chloride is within this range, the mechanical strength can be further increased and sufficient moldability can be ensured.
樹脂組成物は、塩化ビニル系樹脂以外の他の熱可塑性樹脂を含有してもよい。塩化ビニル系樹脂以外の他の熱可塑性樹脂としては、ポリエチレン、ポリプロピレン、ポリスチレン、ポリブテン、塩素化ポリエチレン、エチレン−プロピレン共重合体、エチレン−エチルアクリレート共重合体、ポリエチレンテレフタレート、ABS樹脂、アクリル樹脂等が挙げられる。これらの熱可塑性樹脂は、1種を単独で使用してもよいし、2種以上を併用してもよい。
樹脂組成物において、塩化ビニル系樹脂及び塩化ビニル系樹脂以外の他の熱可塑性樹脂の合計質量に対する塩化ビニル系樹脂の含有量は、70〜100質量%が好ましく、70〜80質量%がより好ましく、70〜75質量%がさらに好ましい。
The resin composition may contain a thermoplastic resin other than the vinyl chloride resin. Examples of thermoplastic resins other than vinyl chloride resins include polyethylene, polypropylene, polystyrene, polybutene, chlorinated polyethylene, ethylene-propylene copolymer, ethylene-ethylacrylate copolymer, polyethylene terephthalate, ABS resin, acrylic resin and the like. Can be mentioned. One of these thermoplastic resins may be used alone, or two or more thereof may be used in combination.
In the resin composition, the content of the vinyl chloride resin with respect to the total mass of the vinyl chloride resin and the thermoplastic resin other than the vinyl chloride resin is preferably 70 to 100% by mass, more preferably 70 to 80% by mass. , 70-75% by mass is more preferable.
樹脂組成物の塩素含有量は、56.6〜58.2質量%であり、57〜58質量%が好ましく、57.2〜57.8質量%がより好ましい。樹脂組成物の塩素含有量がこの範囲内であると、成形時のヤケを抑制できる。
樹脂組成物の塩素含有量は、JIS K 7229:1995「塩素含有樹脂中の塩素の定量方法」に基づき、フラスコ燃焼/滴定により測定したものである。
The chlorine content of the resin composition is 56.6 to 58.2% by mass, preferably 57 to 58% by mass, and more preferably 57.2 to 57.8% by mass. When the chlorine content of the resin composition is within this range, discoloration during molding can be suppressed.
The chlorine content of the resin composition was measured by flask burning / titration based on JIS K 7229: 1995 "Method for quantifying chlorine in chlorine-containing resin".
(安定剤)
樹脂組成物は、塩化ビニル系樹脂の熱分解を抑制する目的で安定剤を含有することが好ましい。安定剤としては、例えば、錫系安定剤、Ca−Zn系安定剤、高級脂肪酸金属塩等が挙げられる。安定剤は、1種を単独で使用してもよいし、2種以上を併用してもよい。ただし、鉛系安定剤を除く。
錫系安定剤としては、例えば、ジブチル錫メルカプト、ジオクチル錫メルカプト、ジメチル錫メルカプト等のメルカプチド類;ジブチル錫マレート、ジブチル錫マレートポリマー、ジオクチル錫マレート、ジオクチル錫マレートポリマー等のマレート類;ジブチル錫メルカプトジブチル錫ラウレート、ジブチル錫ラウレートポリマー等のカルボキシレート類が挙げられる。透明性を担保する観点から、錫系安定剤としては、メルカプト系化合物が好ましい。例えば、ジブチル錫メルカプタン、ジオクチル錫メルカプタン等が挙げられる。錫系安定剤は、1種を単独で使用してもよいし、2種以上を併用してもよい。
Ca−Zn系安定剤はカルシウムの脂肪酸塩と亜鉛の脂肪酸塩との混合物である。脂肪酸としては、ベヘニン酸、ステアリン酸、ラウリン酸、オレイン酸、パルミチン酸、リシノール酸、安息香酸等が挙げられる。Ca−Zn系安定剤は、1種を単独で使用してもよいし、2種以上うぃ併用してもよい。
高級脂肪酸金属塩としては、例えば、ステアリン酸リチウム、ステアリン酸マグネシウム、ステアリン酸カルシウム、ラウリン酸カルシウム、リシノール酸カルシウム、ステアリン酸ストロンチウム、ステアリン酸バリウム、ラウリン酸バリウム、リシノール酸バリウム、ステアリン酸カドミウム、ラウリン酸カドミウム、リシノール酸カドミウム、ナフテン酸カドミウム、2−エチルヘキソイン酸カドミウム、ステアリン酸亜鉛、ラウリン酸亜鉛、リシノール酸亜鉛、2−エチルヘキソイン酸亜鉛、ステアリン酸鉛、二塩基性ステアリン酸鉛、ナフテン酸鉛等が挙げられる。高級脂肪酸金属塩、1種を単独で使用してもよいし、2種以上併用してもよい。
これらの中でも、錫系安定剤が好ましい。塩化ビニル系樹脂の熱安定性をより高め、加工性を向上させる観点から、錫系安定剤を2種以上併用することが好ましい。
(Stabilizer)
The resin composition preferably contains a stabilizer for the purpose of suppressing thermal decomposition of the vinyl chloride resin. Examples of the stabilizer include a tin-based stabilizer, a Ca-Zn-based stabilizer, a higher fatty acid metal salt, and the like. As the stabilizer, one type may be used alone, or two or more types may be used in combination. However, lead-based stabilizers are excluded.
Examples of the tin-based stabilizer include mercaptides such as dibutyltin mercapto, dioctyltin mercapto, and dimethyltin mercapto; malates such as dibutyltin malate, dibutyltin malate polymer, dioctyltin malate, and dioctyltin malate polymer; dibutyl. Examples thereof include carboxylates such as tin mercaptodibutyl tin laurate and dibutyltin laurate polymer. From the viewpoint of ensuring transparency, the tin-based stabilizer is preferably a mercapto-based compound. For example, dibutyl tin mercaptan, dioctyl tin mercaptan and the like can be mentioned. As the tin-based stabilizer, one type may be used alone, or two or more types may be used in combination.
The Ca-Zn-based stabilizer is a mixture of a fatty acid salt of calcium and a fatty acid salt of zinc. Examples of fatty acids include behenic acid, stearic acid, lauric acid, oleic acid, palmitic acid, ricinoleic acid, benzoic acid and the like. As the Ca—Zn-based stabilizer, one type may be used alone, or two or more types may be used in combination.
Examples of the higher fatty acid metal salt include lithium stearate, magnesium stearate, calcium stearate, calcium laurate, calcium ricinolate, strontium stearate, barium stearate, barium laurate, barium ricinolate, cadmium stearate, and cadmium laurate. , Cadmium ricinolate, cadmium naphthenate, cadmium 2-ethylhexoate, zinc stearate, zinc laurate, zinc ricinolate, zinc 2-ethylhexoate, lead stearate, lead dibasic stearate, lead naphthenate, etc. Be done. One type of higher fatty acid metal salt may be used alone, or two or more types may be used in combination.
Among these, tin-based stabilizers are preferable. From the viewpoint of further enhancing the thermal stability of the vinyl chloride resin and improving the processability, it is preferable to use two or more tin stabilizers in combination.
安定剤の含有量は、特に限定されないが、塩化ビニル系樹脂100質量部に対して、1.0〜10.0質量部が好ましく、2.0〜5.0質量部がより好ましい。安定剤の含有量がこの範囲内であると、安定剤が上記範囲内であると成形時のヤケをさらに抑制できる。 The content of the stabilizer is not particularly limited, but is preferably 1.0 to 10.0 parts by mass and more preferably 2.0 to 5.0 parts by mass with respect to 100 parts by mass of the vinyl chloride resin. When the content of the stabilizer is within this range, when the stabilizer is within the above range, discoloration during molding can be further suppressed.
(添加剤)
樹脂組成物には、本発明の効果を損なわない範囲で、改質剤、滑剤、加工助剤、着色剤、無機難燃剤、衝撃改質剤、耐熱向上剤、酸化防止剤、熱安定化助剤、光安定剤、紫外線吸収剤、可塑剤、熱可塑性エラストマー等の添加剤が含まれてもよい。
これらの添加剤(任意成分)は、1種を単独で使用してもよいし、2種以上を併用してもよい。
(Additive)
The resin composition contains a modifier, a lubricant, a processing aid, a colorant, an inorganic flame retardant, an impact modifier, a heat resistance improver, an antioxidant, and a heat stabilization aid as long as the effects of the present invention are not impaired. Additives such as agents, light stabilizers, UV absorbers, plasticizers, thermoplastic elastomers and the like may be included.
One of these additives (arbitrary components) may be used alone, or two or more thereof may be used in combination.
上記任意成分の含有量は、塩化ビニル系樹脂100質量部に対して、30質量部以下が好ましく、20質量部以下がより好ましく、10質量部以下がさらに好ましい。 The content of the optional component is preferably 30 parts by mass or less, more preferably 20 parts by mass or less, and further preferably 10 parts by mass or less with respect to 100 parts by mass of the vinyl chloride resin.
[耐熱透明継手の製造方法]
耐熱透明継手1(2)は、射出成形により製造される。
例えば、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、耐熱透明継手1(2)が得られる。
[Manufacturing method of heat-resistant transparent joint]
The heat-resistant transparent joint 1 (2) is manufactured by injection molding.
For example, the heat-resistant transparent joint 1 (2) is obtained by heating and melting the resin composition, injecting it into a mold, heating it at an arbitrary temperature for an arbitrary time, and cooling it at an arbitrary temperature for an arbitrary time.
射出成形機において、金型内に射出される直前の樹脂組成物の温度(成形温度)は170〜190℃が好ましく、180〜190℃がより好ましい。成形温度が前記範囲内であると塩化ビニル系樹脂の熱分解を抑えつつ十分に溶融させて、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、1〜5分が好ましい。この範囲内であると、スクリュー内のヤケを抑制できる。
In the injection molding machine, the temperature (molding temperature) of the resin composition immediately before being injected into the mold is preferably 170 to 190 ° C, more preferably 180 to 190 ° C. When the molding temperature is within the above range, the vinyl chloride resin is sufficiently melted while suppressing thermal decomposition, and good fluidity of the resin composition can be obtained.
The time for molding with a mold is preferably 1 to 5 minutes. Within this range, discoloration in the screw can be suppressed.
以上、本発明の耐熱透明継手の第1の実施形態及び第2の実施形態について、詳細に説明してきたが、本発明は上述した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。 Although the first embodiment and the second embodiment of the heat-resistant transparent joint of the present invention have been described in detail above, the present invention is not limited to the above-described embodiment and does not deviate from the gist thereof. Can be changed as appropriate.
耐熱透明継手の本体部に形成された開口部は、2つ又は3つに限定されず、4つであってもよく、5つ以上であってもよい。開口部の内径は、他の開口部の内径と同じであってもよく、異なっていてもよい。
樹脂管継手の本体部を管軸方向に垂直な面で切断した断面は、平面視円形であってもよく、平面視楕円形、平面視多角形であってもよい。
樹脂管継手の形状としては、例えば、上記のエルボ、チーズの他にも、ニップル、径違いニップル(レジューサ)、クロス、バルブソケット等が挙げられる。
The number of openings formed in the main body of the heat-resistant transparent joint is not limited to two or three, and may be four or five or more. The inner diameter of the opening may be the same as or different from the inner diameter of the other openings.
The cross section of the main body of the resin pipe joint cut along a plane perpendicular to the pipe axis direction may be circular in a plan view, elliptical in a plan view, or polygon in a plan view.
Examples of the shape of the resin pipe joint include nipples, nipples with different diameters (reducers), cloths, valve sockets, and the like, in addition to the above elbows and cheeses.
以上、説明してきたように、本発明の耐熱透明継手は、成形時に生じるヤケが低減された大口径の耐熱透明継手である。ヤケが低減されていることから、本発明の耐熱透明継手の受入部は透明であり、継手内部の管の挿入状態を確認することができ、管が継手の受入部に固定されていることを容易に、かつ、確実に視認可能とすることができる。 As described above, the heat-resistant transparent joint of the present invention is a large-diameter heat-resistant transparent joint in which discoloration caused during molding is reduced. Since the discoloration is reduced, the receiving portion of the heat-resistant transparent joint of the present invention is transparent, the inserted state of the pipe inside the joint can be confirmed, and the pipe is fixed to the receiving portion of the joint. It can be easily and surely made visible.
以下では、実施例により本発明をより具体的に説明するが、本発明はこれらの実施例に限定されるものではなく、本発明の要旨を変更しない限り、種々の変形が可能である。 Hereinafter, the present invention will be described in more detail with reference to Examples, but the present invention is not limited to these Examples, and various modifications are possible as long as the gist of the present invention is not changed.
[実施例1]
塩化ビニル系樹脂(塩素化塩化ビニル、セキスイCPVC HA−27H、徳山積水工業社製)100質量部と、安定剤(ジオクチル錫メルカプト、ONZ−142AF、日東化成社製)4.0質量部と、任意成分(改質剤、滑剤、加工助剤、着色剤)9.6質量部と、を配合した後、内容積200Lの辺シェルミキサー(川田工業社製)を用い、撹拌混合して樹脂組成物を得た。樹脂組成物の組成を表1に示す。
得られた樹脂組成物を射出成形して、図3に示す形状のチーズ(ティー)型の継手を製造した。受入部は呼び径が75〜100である管の端部を差込み可能なサイズとした。成形温度は175℃、金型温度は20℃、成形時間は100秒とした。
得られた継手は、本体部が不透明の白色であり、受入部は透明の黄色であった。
得られた継手について、以下の試験を行った。
[Example 1]
100 parts by mass of vinyl chloride resin (vinyl chloride, Sekisui CPVC HA-27H, manufactured by Tokuyama Sekisui Kogyo Co., Ltd.), 4.0 parts by mass of stabilizer (Dioctyl tin mercapto, ONZ-142AF, manufactured by Nitto Kasei Co., Ltd.), After blending 9.6 parts by mass of optional components (modifier, lubricant, processing aid, colorant), the resin composition is mixed by stirring using a side shell mixer (manufactured by Kawada Kogyo Co., Ltd.) with an internal volume of 200 L. I got something. The composition of the resin composition is shown in Table 1.
The obtained resin composition was injection-molded to produce a cheese (tea) -shaped joint having the shape shown in FIG. The receiving portion has a size that allows the end of a pipe having a nominal diameter of 75 to 100 to be inserted. The molding temperature was 175 ° C., the mold temperature was 20 ° C., and the molding time was 100 seconds.
The obtained joint had an opaque white body and a transparent yellow receiving part.
The following tests were performed on the obtained joints.
<塩素含有量>
JIS K 7229:1995「塩素含有樹脂中の塩素の定量方法」に基づき、フラスコ燃焼/滴定により塩素含有量(単位:質量%)を測定した。
測定結果を表1に示す。
<Chlorine content>
The chlorine content (unit: mass%) was measured by flask burning / titration based on JIS K 7229: 1995 "Method for quantifying chlorine in chlorine-containing resin".
The measurement results are shown in Table 1.
<透明性>
JIS K 7135:2000「プラスチック−透明材料のヘーズの求め方」に従って、製造した継手の受入部のヘイズ値を測定した。
以下の基準に従って、継手の受入部の透明性を評価した。
○:ヘイズ値が20〜80である
×:ヘイズ値が80超である
<Transparency>
The haze value of the receiving part of the manufactured joint was measured according to JIS K 7135: 2000 “Plastic-How to determine the haze of transparent material”.
The transparency of the receiving part of the joint was evaluated according to the following criteria.
◯: Haze value is 20 to 80 ×: Haze value is more than 80
<耐熱性>
JIS K 7206:2016「プラスチック−熱可塑性プラスチック−ビカット軟化温度(VST)の求め方」に従って、製造した継手のビカット軟化温度を測定した。
以下の基準に従って、継手の耐熱性を評価した。
○:ビカット軟化温度が90℃以上である
×:ビカット軟化温度が90℃未満である
評価結果を表1に示す。
<Heat resistance>
The Vicat softening temperature of the manufactured joint was measured according to JIS K 7206: 2016 "Plastic-Thermoplastic Plastic-How to Obtain the Vicat Softening Temperature (VST)".
The heat resistance of the joint was evaluated according to the following criteria.
◯: Vicat softening temperature is 90 ° C. or higher ×: Vicat softening temperature is less than 90 ° C. The evaluation results are shown in Table 1.
<耐ヤケ性>
製造した継手の外観を目視で観察して、変色の有無とヤケの有無を確認した。
以下の基準に従って、継手の耐ヤケ性を評価した。
○:ヤケがない
×:ヤケがある
評価結果を表1に示す。
<Burning resistance>
The appearance of the manufactured joint was visually observed to confirm the presence or absence of discoloration and the presence or absence of discoloration.
The burn resistance of the joint was evaluated according to the following criteria.
◯: No burns ×: Burns The evaluation results are shown in Table 1.
<総合評価>
耐熱性及び耐ヤケ性に基づいて、以下の基準に従って、総合評価を行った。
○:透明性、耐熱性及び耐ヤケ性の評価のすべてが「〇」である
×:透明性、耐熱性及び耐ヤケ性の評価のうち1つ以上が「×」である
評価結果を表1に示す。
<Comprehensive evaluation>
Comprehensive evaluation was performed according to the following criteria based on heat resistance and burn resistance.
◯: All evaluations of transparency, heat resistance and burn resistance are “○” ×: Evaluation results of one or more of the evaluations of transparency, heat resistance and burn resistance are “×” Table 1 Shown in.
[実施例2]
塩化ビニル系樹脂として、塩素化塩化ビニル(セキスイCPVC HA−27F、徳山積水工業社製)を用いた点を除いて、実施例1と同様にして継手を製造し、透明性、耐熱性及び耐ヤケ性を評価し、総合評価を行った。評価結果を表1に示す。
[Example 2]
A joint was manufactured in the same manner as in Example 1 except that chlorinated vinyl chloride (Sekisui CPVC HA-27F, manufactured by Tokuyama Sekisui Kogyo Co., Ltd.) was used as the vinyl chloride resin, and transparency, heat resistance and resistance were obtained. The discoloration was evaluated and a comprehensive evaluation was performed. The evaluation results are shown in Table 1.
[比較例1]
塩化ビニル系樹脂として、塩素化塩化ビニル(セキスイCPVC HA−27K、徳山積水工業社製)を用いた点を除いて、実施例1と同様にして継手を製造し、透明性、耐熱性及び耐ヤケ性を評価し、総合評価を行った。評価結果を表1に示す。
[Comparative Example 1]
A joint was manufactured in the same manner as in Example 1 except that chlorinated vinyl chloride (Sekisui CPVC HA-27K, manufactured by Tokuyama Sekisui Kogyo Co., Ltd.) was used as the vinyl chloride resin, and transparency, heat resistance and resistance were obtained. The discoloration was evaluated and a comprehensive evaluation was performed. The evaluation results are shown in Table 1.
表1中、塩化ビニル系樹脂、安定剤及び配合剤は以下のとおりである。
・塩化ビニル系樹脂
H: 塩素化塩化ビニル(セキスイCPVC HA−27H、徳山積水工業社製、塩素化度65.5質量%)
F: 塩素化塩化ビニル(セキスイCPVC HA−27F、徳山積水工業社製、塩素化度64.5質量%)
K: 塩素化塩化ビニル(セキスイCPVC HA−27K、徳山積水工業社製、塩素化度66.5質量%)
・安定剤
ジオクチル錫メルカプト(ONZ−142AF、日東化成社製)
In Table 1, vinyl chloride resins, stabilizers and compounding agents are as follows.
-Vinyl chloride resin H: Chlorinated vinyl chloride (Sekisui CPVC HA-27H, manufactured by Tokuyama Sekisui Kogyo Co., Ltd., chlorination degree 65.5% by mass)
F: Chlorinated vinyl chloride (Sekisui CPVC HA-27F, manufactured by Tokuyama Sekisui Kogyo Co., Ltd., chlorination degree 64.5% by mass)
K: Vinyl chloride chlorinated (Sekisui CPVC HA-27K, manufactured by Tokuyama Sekisui Kogyo Co., Ltd., degree of chlorination 66.5% by mass)
・ Stabilizer Dioctyl tin mercapto (ONZ-142AF, manufactured by Nitto Kasei Co., Ltd.)
[結果の説明]
実施例1、2の継手は、耐熱性及び耐ヤケ性が要求水準を満たしており、総合評価も良好(○)であった。
比較例1の継手は、耐熱性は十分(評価:〇)であったが、透明性及び耐ヤケ性が不十分(評価:×)であり、総合評価は不合格(×)であった。
本発明によれば、成形時に生じるヤケが低減された大口径の耐熱透明継手を提供できる。
[Explanation of results]
The joints of Examples 1 and 2 satisfied the required levels of heat resistance and burn resistance, and the overall evaluation was also good (◯).
The joint of Comparative Example 1 had sufficient heat resistance (evaluation: 〇), but had insufficient transparency and burn resistance (evaluation: ×), and the overall evaluation was unacceptable (×).
According to the present invention, it is possible to provide a large-diameter heat-resistant transparent joint in which discoloration caused during molding is reduced.
1、2 耐熱透明継手
10、20 本体部
11、21 受入部
11a、21a 第1の受入部
11b、21b 第2の受入部
21c 第3の受入部
12、22 開口部
12a、22a 第1の開口部
12b、22b 第2の開口部
22c 第3の開口部
13、23 受入部の開口部
13a、23a 受入部の第1の開口部
13b、23b 受入部の第2の開口部
23c 受入部の第3の開口部
14、24 流路
O1 第1の管軸
O2 第2の管軸
1, 2 Heat-resistant
Claims (4)
前記本体部及び前記受入部は、塩化ビニル系樹脂を含む、塩素含有量が56.6〜58.2質量%である樹脂組成物からなり、
前記受入部のうち少なくとも1つは、呼び径が75〜100である管の端部を差込み可能である、耐熱透明継手。 A main body having a flow path inside and having two or more openings formed therein, and a receiving portion surrounding the peripheral edge of the opening of the main body are provided.
The main body portion and the receiving portion are made of a resin composition containing a vinyl chloride resin and having a chlorine content of 56.6 to 58.2% by mass.
At least one of the receiving portions is a heat-resistant transparent joint into which an end portion of a pipe having a nominal diameter of 75 to 100 can be inserted.
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