JPS6234781B2 - - Google Patents
Info
- Publication number
- JPS6234781B2 JPS6234781B2 JP6136578A JP6136578A JPS6234781B2 JP S6234781 B2 JPS6234781 B2 JP S6234781B2 JP 6136578 A JP6136578 A JP 6136578A JP 6136578 A JP6136578 A JP 6136578A JP S6234781 B2 JPS6234781 B2 JP S6234781B2
- Authority
- JP
- Japan
- Prior art keywords
- weather
- resistant polymer
- ethylene
- sheet
- component
- 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.)
- Expired
Links
- 229920000642 polymer Polymers 0.000 claims description 28
- 230000001070 adhesive effect Effects 0.000 claims description 21
- 239000000203 mixture Substances 0.000 claims description 17
- -1 pseudohalogen compound Chemical class 0.000 claims description 14
- 229920001577 copolymer Polymers 0.000 claims description 8
- 229910052736 halogen Inorganic materials 0.000 claims description 6
- 150000002367 halogens Chemical class 0.000 claims description 6
- 229920005989 resin Polymers 0.000 claims description 6
- 239000011347 resin Substances 0.000 claims description 6
- 229920006242 ethylene acrylic acid copolymer Polymers 0.000 claims description 5
- 229920002589 poly(vinylethylene) polymer Polymers 0.000 claims description 5
- 239000004698 Polyethylene Substances 0.000 claims description 4
- 229910021645 metal ion Inorganic materials 0.000 claims description 3
- 229920000573 polyethylene Polymers 0.000 claims description 3
- 229920002367 Polyisobutene Polymers 0.000 claims description 2
- 239000005038 ethylene vinyl acetate Substances 0.000 claims description 2
- CSCPPACGZOOCGX-UHFFFAOYSA-N Acetone Chemical compound CC(C)=O CSCPPACGZOOCGX-UHFFFAOYSA-N 0.000 description 20
- 239000000853 adhesive Substances 0.000 description 19
- 238000012360 testing method Methods 0.000 description 17
- ZWEHNKRNPOVVGH-UHFFFAOYSA-N 2-Butanone Chemical compound CCC(C)=O ZWEHNKRNPOVVGH-UHFFFAOYSA-N 0.000 description 12
- 239000004636 vulcanized rubber Substances 0.000 description 11
- 238000011282 treatment Methods 0.000 description 10
- WYURNTSHIVDZCO-UHFFFAOYSA-N Tetrahydrofuran Chemical compound C1CCOC1 WYURNTSHIVDZCO-UHFFFAOYSA-N 0.000 description 8
- 239000003795 chemical substances by application Substances 0.000 description 8
- 239000000243 solution Substances 0.000 description 8
- XEEYBQQBJWHFJM-UHFFFAOYSA-N Iron Chemical compound [Fe] XEEYBQQBJWHFJM-UHFFFAOYSA-N 0.000 description 7
- 230000006866 deterioration Effects 0.000 description 7
- UHOVQNZJYSORNB-UHFFFAOYSA-N Benzene Chemical compound C1=CC=CC=C1 UHOVQNZJYSORNB-UHFFFAOYSA-N 0.000 description 6
- XEKOWRVHYACXOJ-UHFFFAOYSA-N Ethyl acetate Chemical compound CCOC(C)=O XEKOWRVHYACXOJ-UHFFFAOYSA-N 0.000 description 6
- YXFVVABEGXRONW-UHFFFAOYSA-N Toluene Chemical compound CC1=CC=CC=C1 YXFVVABEGXRONW-UHFFFAOYSA-N 0.000 description 6
- 125000002577 pseudohalo group Chemical group 0.000 description 6
- CBENFWSGALASAD-UHFFFAOYSA-N Ozone Chemical compound [O-][O+]=O CBENFWSGALASAD-UHFFFAOYSA-N 0.000 description 5
- 239000002184 metal Substances 0.000 description 5
- 229910052751 metal Inorganic materials 0.000 description 5
- 238000000034 method Methods 0.000 description 5
- 230000000704 physical effect Effects 0.000 description 5
- IBOFVQJTBBUKMU-UHFFFAOYSA-N 4,4'-methylene-bis-(2-chloroaniline) Chemical compound C1=C(Cl)C(N)=CC=C1CC1=CC=C(N)C(Cl)=C1 IBOFVQJTBBUKMU-UHFFFAOYSA-N 0.000 description 4
- HEDRZPFGACZZDS-UHFFFAOYSA-N Chloroform Chemical compound ClC(Cl)Cl HEDRZPFGACZZDS-UHFFFAOYSA-N 0.000 description 4
- 229920002943 EPDM rubber Polymers 0.000 description 4
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 4
- RTZKZFJDLAIYFH-UHFFFAOYSA-N ether Substances CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 description 4
- 229910052717 sulfur Inorganic materials 0.000 description 4
- 239000011593 sulfur Substances 0.000 description 4
- 238000004381 surface treatment Methods 0.000 description 4
- YLQBMQCUIZJEEH-UHFFFAOYSA-N tetrahydrofuran Natural products C=1C=COC=1 YLQBMQCUIZJEEH-UHFFFAOYSA-N 0.000 description 4
- YMWUJEATGCHHMB-UHFFFAOYSA-N Dichloromethane Chemical compound ClCCl YMWUJEATGCHHMB-UHFFFAOYSA-N 0.000 description 3
- LYCAIKOWRPUZTN-UHFFFAOYSA-N Ethylene glycol Chemical compound OCCO LYCAIKOWRPUZTN-UHFFFAOYSA-N 0.000 description 3
- 241001112258 Moca Species 0.000 description 3
- NINIDFKCEFEMDL-UHFFFAOYSA-N Sulfur Chemical compound [S] NINIDFKCEFEMDL-UHFFFAOYSA-N 0.000 description 3
- 229920001971 elastomer Polymers 0.000 description 3
- 229910052742 iron Inorganic materials 0.000 description 3
- 239000012948 isocyanate Substances 0.000 description 3
- 150000002513 isocyanates Chemical class 0.000 description 3
- VLKZOEOYAKHREP-UHFFFAOYSA-N n-Hexane Chemical compound CCCCCC VLKZOEOYAKHREP-UHFFFAOYSA-N 0.000 description 3
- 239000005060 rubber Substances 0.000 description 3
- 239000002904 solvent Substances 0.000 description 3
- 229920003051 synthetic elastomer Polymers 0.000 description 3
- RYHBNJHYFVUHQT-UHFFFAOYSA-N 1,4-Dioxane Chemical compound C1COCCO1 RYHBNJHYFVUHQT-UHFFFAOYSA-N 0.000 description 2
- RSWGJHLUYNHPMX-UHFFFAOYSA-N Abietic-Saeure Natural products C12CCC(C(C)C)=CC2=CCC2C1(C)CCCC2(C)C(O)=O RSWGJHLUYNHPMX-UHFFFAOYSA-N 0.000 description 2
- VTYYLEPIZMXCLO-UHFFFAOYSA-L Calcium carbonate Chemical compound [Ca+2].[O-]C([O-])=O VTYYLEPIZMXCLO-UHFFFAOYSA-L 0.000 description 2
- VEXZGXHMUGYJMC-UHFFFAOYSA-M Chloride anion Chemical compound [Cl-] VEXZGXHMUGYJMC-UHFFFAOYSA-M 0.000 description 2
- LCGLNKUTAGEVQW-UHFFFAOYSA-N Dimethyl ether Chemical compound COC LCGLNKUTAGEVQW-UHFFFAOYSA-N 0.000 description 2
- IMNFDUFMRHMDMM-UHFFFAOYSA-N N-Heptane Chemical compound CCCCCCC IMNFDUFMRHMDMM-UHFFFAOYSA-N 0.000 description 2
- OUBMGJOQLXMSNT-UHFFFAOYSA-N N-isopropyl-N'-phenyl-p-phenylenediamine Chemical compound C1=CC(NC(C)C)=CC=C1NC1=CC=CC=C1 OUBMGJOQLXMSNT-UHFFFAOYSA-N 0.000 description 2
- RHYBFKMFHLPQPH-UHFFFAOYSA-N N-methylhydantoin Chemical class CN1CC(=O)NC1=O RHYBFKMFHLPQPH-UHFFFAOYSA-N 0.000 description 2
- 229920000459 Nitrile rubber Polymers 0.000 description 2
- OFBQJSOFQDEBGM-UHFFFAOYSA-N Pentane Chemical compound CCCCC OFBQJSOFQDEBGM-UHFFFAOYSA-N 0.000 description 2
- 239000005062 Polybutadiene Substances 0.000 description 2
- KHPCPRHQVVSZAH-HUOMCSJISA-N Rosin Natural products O(C/C=C/c1ccccc1)[C@H]1[C@H](O)[C@@H](O)[C@@H](O)[C@@H](CO)O1 KHPCPRHQVVSZAH-HUOMCSJISA-N 0.000 description 2
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 description 2
- 235000021355 Stearic acid Nutrition 0.000 description 2
- 229920003182 Surlyn® Polymers 0.000 description 2
- XLOMVQKBTHCTTD-UHFFFAOYSA-N Zinc monoxide Chemical compound [Zn]=O XLOMVQKBTHCTTD-UHFFFAOYSA-N 0.000 description 2
- 125000000217 alkyl group Chemical group 0.000 description 2
- 239000007864 aqueous solution Substances 0.000 description 2
- 150000001875 compounds Chemical class 0.000 description 2
- 150000007973 cyanuric acids Chemical class 0.000 description 2
- JHIVVAPYMSGYDF-UHFFFAOYSA-N cyclohexanone Chemical compound O=C1CCCCC1 JHIVVAPYMSGYDF-UHFFFAOYSA-N 0.000 description 2
- 230000007423 decrease Effects 0.000 description 2
- 230000000694 effects Effects 0.000 description 2
- 239000000463 material Substances 0.000 description 2
- LQNUZADURLCDLV-UHFFFAOYSA-N nitrobenzene Chemical compound [O-][N+](=O)C1=CC=CC=C1 LQNUZADURLCDLV-UHFFFAOYSA-N 0.000 description 2
- QIQXTHQIDYTFRH-UHFFFAOYSA-N octadecanoic acid Chemical compound CCCCCCCCCCCCCCCCCC(O)=O QIQXTHQIDYTFRH-UHFFFAOYSA-N 0.000 description 2
- OQCDKBAXFALNLD-UHFFFAOYSA-N octadecanoic acid Natural products CCCCCCCC(C)CCCCCCCCC(O)=O OQCDKBAXFALNLD-UHFFFAOYSA-N 0.000 description 2
- 239000003960 organic solvent Substances 0.000 description 2
- 239000012188 paraffin wax Substances 0.000 description 2
- 229920002857 polybutadiene Polymers 0.000 description 2
- 239000010734 process oil Substances 0.000 description 2
- 238000012545 processing Methods 0.000 description 2
- 239000008117 stearic acid Substances 0.000 description 2
- 239000005061 synthetic rubber Substances 0.000 description 2
- VZGDMQKNWNREIO-UHFFFAOYSA-N tetrachloromethane Chemical compound ClC(Cl)(Cl)Cl VZGDMQKNWNREIO-UHFFFAOYSA-N 0.000 description 2
- KHPCPRHQVVSZAH-UHFFFAOYSA-N trans-cinnamyl beta-D-glucopyranoside Natural products OC1C(O)C(O)C(CO)OC1OCC=CC1=CC=CC=C1 KHPCPRHQVVSZAH-UHFFFAOYSA-N 0.000 description 2
- 238000004073 vulcanization Methods 0.000 description 2
- 239000011787 zinc oxide Substances 0.000 description 2
- 235000014692 zinc oxide Nutrition 0.000 description 2
- YRIZYWQGELRKNT-UHFFFAOYSA-N 1,3,5-trichloro-1,3,5-triazinane-2,4,6-trione Chemical compound ClN1C(=O)N(Cl)C(=O)N(Cl)C1=O YRIZYWQGELRKNT-UHFFFAOYSA-N 0.000 description 1
- KPZGRMZPZLOPBS-UHFFFAOYSA-N 1,3-dichloro-2,2-bis(chloromethyl)propane Chemical compound ClCC(CCl)(CCl)CCl KPZGRMZPZLOPBS-UHFFFAOYSA-N 0.000 description 1
- XCDWWLVEINTHLA-UHFFFAOYSA-N 1-(dichloromethyl)imidazolidine-2,4-dione Chemical compound ClC(Cl)N1CC(=O)NC1=O XCDWWLVEINTHLA-UHFFFAOYSA-N 0.000 description 1
- RFKBZTZZYCOHTK-UHFFFAOYSA-N 1-phenylpropan-2-yl n,n-dibromocarbamate Chemical compound BrN(Br)C(=O)OC(C)CC1=CC=CC=C1 RFKBZTZZYCOHTK-UHFFFAOYSA-N 0.000 description 1
- YIVBHISFBAZKNU-UHFFFAOYSA-N 1-phenylpropan-2-yl n,n-dichlorocarbamate Chemical compound ClN(Cl)C(=O)OC(C)CC1=CC=CC=C1 YIVBHISFBAZKNU-UHFFFAOYSA-N 0.000 description 1
- MHKLKWCYGIBEQF-UHFFFAOYSA-N 4-(1,3-benzothiazol-2-ylsulfanyl)morpholine Chemical compound C1COCCN1SC1=NC2=CC=CC=C2S1 MHKLKWCYGIBEQF-UHFFFAOYSA-N 0.000 description 1
- ZCYVEMRRCGMTRW-UHFFFAOYSA-N 7553-56-2 Chemical compound [I] ZCYVEMRRCGMTRW-UHFFFAOYSA-N 0.000 description 1
- 229920002126 Acrylic acid copolymer Polymers 0.000 description 1
- ZXFDSSZCWQFXAT-UHFFFAOYSA-N Br.[N-]=[N+]=[N-] Chemical compound Br.[N-]=[N+]=[N-] ZXFDSSZCWQFXAT-UHFFFAOYSA-N 0.000 description 1
- WKBOTKDWSSQWDR-UHFFFAOYSA-N Bromine atom Chemical compound [Br] WKBOTKDWSSQWDR-UHFFFAOYSA-N 0.000 description 1
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 description 1
- 229920000298 Cellophane Polymers 0.000 description 1
- ZAMOUSCENKQFHK-UHFFFAOYSA-N Chlorine atom Chemical compound [Cl] ZAMOUSCENKQFHK-UHFFFAOYSA-N 0.000 description 1
- XDTMQSROBMDMFD-UHFFFAOYSA-N Cyclohexane Chemical compound C1CCCCC1 XDTMQSROBMDMFD-UHFFFAOYSA-N 0.000 description 1
- VGGSQFUCUMXWEO-UHFFFAOYSA-N Ethene Chemical compound C=C VGGSQFUCUMXWEO-UHFFFAOYSA-N 0.000 description 1
- JOYRKODLDBILNP-UHFFFAOYSA-N Ethyl urethane Chemical compound CCOC(N)=O JOYRKODLDBILNP-UHFFFAOYSA-N 0.000 description 1
- 239000005977 Ethylene Substances 0.000 description 1
- XWAIXCWZEDDKHO-UHFFFAOYSA-N I.OC(=O)C(Cl)(Cl)Cl Chemical compound I.OC(=O)C(Cl)(Cl)Cl XWAIXCWZEDDKHO-UHFFFAOYSA-N 0.000 description 1
- QZRGKCOWNLSUDK-UHFFFAOYSA-N Iodochlorine Chemical compound ICl QZRGKCOWNLSUDK-UHFFFAOYSA-N 0.000 description 1
- 239000004157 Nitrosyl chloride Substances 0.000 description 1
- CTQNGGLPUBDAKN-UHFFFAOYSA-N O-Xylene Chemical compound CC1=CC=CC=C1C CTQNGGLPUBDAKN-UHFFFAOYSA-N 0.000 description 1
- 239000004743 Polypropylene Substances 0.000 description 1
- DKGAVHZHDRPRBM-UHFFFAOYSA-N Tert-Butanol Chemical compound CC(C)(C)O DKGAVHZHDRPRBM-UHFFFAOYSA-N 0.000 description 1
- NRVCVLFVSDRPOM-UHFFFAOYSA-N [I+].[O-][N+]([O-])=O Chemical compound [I+].[O-][N+]([O-])=O NRVCVLFVSDRPOM-UHFFFAOYSA-N 0.000 description 1
- HHJKEJPPPVBHIZ-UHFFFAOYSA-N [N-]=[N+]=[N-].I Chemical compound [N-]=[N+]=[N-].I HHJKEJPPPVBHIZ-UHFFFAOYSA-N 0.000 description 1
- MNZMECMQTYGSOI-UHFFFAOYSA-N acetic acid;hydron;bromide Chemical compound Br.CC(O)=O MNZMECMQTYGSOI-UHFFFAOYSA-N 0.000 description 1
- 239000002253 acid Substances 0.000 description 1
- 150000001298 alcohols Chemical class 0.000 description 1
- 150000001338 aliphatic hydrocarbons Chemical class 0.000 description 1
- 150000004945 aromatic hydrocarbons Chemical class 0.000 description 1
- 150000001555 benzenes Chemical class 0.000 description 1
- GDTBXPJZTBHREO-UHFFFAOYSA-N bromine Substances BrBr GDTBXPJZTBHREO-UHFFFAOYSA-N 0.000 description 1
- 229910052794 bromium Inorganic materials 0.000 description 1
- FWRXDHNZNSQIIY-UHFFFAOYSA-N butan-2-yl n,n-dibromocarbamate Chemical compound CCC(C)OC(=O)N(Br)Br FWRXDHNZNSQIIY-UHFFFAOYSA-N 0.000 description 1
- LQIHFGJIROIECY-UHFFFAOYSA-N butan-2-yl n,n-dichlorocarbamate Chemical compound CCC(C)OC(=O)N(Cl)Cl LQIHFGJIROIECY-UHFFFAOYSA-N 0.000 description 1
- 229910000019 calcium carbonate Inorganic materials 0.000 description 1
- 239000000378 calcium silicate Substances 0.000 description 1
- 229910052918 calcium silicate Inorganic materials 0.000 description 1
- OYACROKNLOSFPA-UHFFFAOYSA-N calcium;dioxido(oxo)silane Chemical compound [Ca+2].[O-][Si]([O-])=O OYACROKNLOSFPA-UHFFFAOYSA-N 0.000 description 1
- 229910052799 carbon Inorganic materials 0.000 description 1
- 239000006229 carbon black Substances 0.000 description 1
- 239000004568 cement Substances 0.000 description 1
- 239000000460 chlorine Substances 0.000 description 1
- 229910052801 chlorine Inorganic materials 0.000 description 1
- 239000011162 core material Substances 0.000 description 1
- 150000004292 cyclic ethers Chemical class 0.000 description 1
- VRLDVERQJMEPIF-UHFFFAOYSA-N dbdmh Chemical compound CC1(C)N(Br)C(=O)N(Br)C1=O VRLDVERQJMEPIF-UHFFFAOYSA-N 0.000 description 1
- 238000010586 diagram Methods 0.000 description 1
- CEJLBZWIKQJOAT-UHFFFAOYSA-N dichloroisocyanuric acid Chemical compound ClN1C(=O)NC(=O)N(Cl)C1=O CEJLBZWIKQJOAT-UHFFFAOYSA-N 0.000 description 1
- 150000001993 dienes Chemical class 0.000 description 1
- 238000007598 dipping method Methods 0.000 description 1
- 238000001035 drying Methods 0.000 description 1
- 239000003822 epoxy resin Substances 0.000 description 1
- 150000002148 esters Chemical class 0.000 description 1
- 229920001038 ethylene copolymer Polymers 0.000 description 1
- 238000011156 evaluation Methods 0.000 description 1
- 238000002474 experimental method Methods 0.000 description 1
- 239000000835 fiber Substances 0.000 description 1
- 239000000945 filler Substances 0.000 description 1
- 239000011521 glass Substances 0.000 description 1
- 239000003365 glass fiber Substances 0.000 description 1
- 150000008282 halocarbons Chemical class 0.000 description 1
- 229930195733 hydrocarbon Natural products 0.000 description 1
- 150000002430 hydrocarbons Chemical class 0.000 description 1
- CUILPNURFADTPE-UHFFFAOYSA-N hypobromous acid Chemical compound BrO CUILPNURFADTPE-UHFFFAOYSA-N 0.000 description 1
- QWPPOHNGKGFGJK-UHFFFAOYSA-N hypochlorous acid Chemical compound ClO QWPPOHNGKGFGJK-UHFFFAOYSA-N 0.000 description 1
- PNDPGZBMCMUPRI-UHFFFAOYSA-N iodine Chemical compound II PNDPGZBMCMUPRI-UHFFFAOYSA-N 0.000 description 1
- 229910052740 iodine Inorganic materials 0.000 description 1
- 239000011630 iodine Substances 0.000 description 1
- CBEQRNSPHCCXSH-UHFFFAOYSA-N iodine monobromide Chemical compound IBr CBEQRNSPHCCXSH-UHFFFAOYSA-N 0.000 description 1
- 150000002576 ketones Chemical class 0.000 description 1
- 229920005610 lignin Polymers 0.000 description 1
- 229920001684 low density polyethylene Polymers 0.000 description 1
- 239000004702 low-density polyethylene Substances 0.000 description 1
- QSHDDOUJBYECFT-UHFFFAOYSA-N mercury Chemical compound [Hg] QSHDDOUJBYECFT-UHFFFAOYSA-N 0.000 description 1
- 229910052753 mercury Inorganic materials 0.000 description 1
- 239000002905 metal composite material Substances 0.000 description 1
- 239000002480 mineral oil Substances 0.000 description 1
- 235000010446 mineral oil Nutrition 0.000 description 1
- 238000002156 mixing Methods 0.000 description 1
- 238000000465 moulding Methods 0.000 description 1
- VXPPIKJLVXUAFT-UHFFFAOYSA-N n,n-dibromo-1-phenylmethanesulfonamide Chemical compound BrN(Br)S(=O)(=O)CC1=CC=CC=C1 VXPPIKJLVXUAFT-UHFFFAOYSA-N 0.000 description 1
- FWPQTIYBQZKGLY-UHFFFAOYSA-N n,n-dichloro-1-phenylmethanesulfonamide Chemical compound ClN(Cl)S(=O)(=O)CC1=CC=CC=C1 FWPQTIYBQZKGLY-UHFFFAOYSA-N 0.000 description 1
- 229940032017 n-oxydiethylene-2-benzothiazole sulfenamide Drugs 0.000 description 1
- BMNDJWSIKZECMH-UHFFFAOYSA-N nitrosyl bromide Chemical compound BrN=O BMNDJWSIKZECMH-UHFFFAOYSA-N 0.000 description 1
- VPCDQGACGWYTMC-UHFFFAOYSA-N nitrosyl chloride Chemical compound ClN=O VPCDQGACGWYTMC-UHFFFAOYSA-N 0.000 description 1
- 235000019392 nitrosyl chloride Nutrition 0.000 description 1
- TVMXDCGIABBOFY-UHFFFAOYSA-N octane Chemical compound CCCCCCCC TVMXDCGIABBOFY-UHFFFAOYSA-N 0.000 description 1
- PUXOVNZJVXQFBO-UHFFFAOYSA-N pentan-2-yl n,n-dibromocarbamate Chemical compound CCCC(C)OC(=O)N(Br)Br PUXOVNZJVXQFBO-UHFFFAOYSA-N 0.000 description 1
- ACAVCPDLJLYGIJ-UHFFFAOYSA-N pentan-2-yl n,n-dichlorocarbamate Chemical compound CCCC(C)OC(=O)N(Cl)Cl ACAVCPDLJLYGIJ-UHFFFAOYSA-N 0.000 description 1
- 150000002978 peroxides Chemical class 0.000 description 1
- 239000004033 plastic Substances 0.000 description 1
- 239000004014 plasticizer Substances 0.000 description 1
- 229920000647 polyepoxide Polymers 0.000 description 1
- 229920001155 polypropylene Polymers 0.000 description 1
- 229920002635 polyurethane Polymers 0.000 description 1
- 239000004814 polyurethane Substances 0.000 description 1
- 229920005749 polyurethane resin Polymers 0.000 description 1
- 239000012779 reinforcing material Substances 0.000 description 1
- 239000000377 silicon dioxide Substances 0.000 description 1
- 229910001415 sodium ion Inorganic materials 0.000 description 1
- 238000005507 spraying Methods 0.000 description 1
- 238000010186 staining Methods 0.000 description 1
- 229950009390 symclosene Drugs 0.000 description 1
- IXZDIALLLMRYOU-UHFFFAOYSA-N tert-butyl hypochlorite Chemical compound CC(C)(C)OCl IXZDIALLLMRYOU-UHFFFAOYSA-N 0.000 description 1
- 229920002803 thermoplastic polyurethane Polymers 0.000 description 1
- DTMHTVJOHYTUHE-UHFFFAOYSA-N thiocyanogen Chemical compound N#CSSC#N DTMHTVJOHYTUHE-UHFFFAOYSA-N 0.000 description 1
- 150000003673 urethanes Chemical class 0.000 description 1
- 235000015112 vegetable and seed oil Nutrition 0.000 description 1
- 239000008158 vegetable oil Substances 0.000 description 1
- 239000008096 xylene Substances 0.000 description 1
Landscapes
- Compositions Of Macromolecular Compounds (AREA)
- Manufacture Of Macromolecular Shaped Articles (AREA)
- Treatments Of Macromolecular Shaped Articles (AREA)
Description
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The present invention relates to a weather-resistant polymer sheet with good adhesion. There are many polymers such as polyethylene and polypropylene that have good weather resistance, especially resistance to ozone deterioration, but a common drawback of these polymers is that they cannot be used together or with other materials. It is difficult to adhere. Conventionally, surface treatments such as corona discharge and buffing have been performed to improve the adhesion of various materials made of these polymers, but these methods are complicated and have little effect, so they are not generally recommended methods. It's hard to say. Therefore, weather-resistant polymers are used only in specific areas that do not require adhesive operations or do not require significant adhesive strength, and are used in adhesive applications to enable more widespread use in areas that require weather resistance. It was hoped to improve sexuality. Based on the above background, the present invention aims to provide a sheet made of a polymer composition that has good adhesiveness and good weather resistance. That is, the present invention has a weather-resistant polymer and a 1,2-polybutadiene resin as the second component as essential components, and the ratio of the weather-resistant polymer to the second component is 80:
The present invention relates to a weather-resistant polymer composition with good adhesion, characterized in that the surface of the sheet is treated with a halogen molecule or a pseudohalogen compound in a weight ratio of 20 to 10:90. The weather-resistant polymer that is the first component used in the composition of the present invention includes polyethylene, polypropylene, ethylene-vinyl acetate copolymer, ethylene-propylene copolymer, ethylene-acrylic acid copolymer,
In addition to single polymers and copolymers that do not substantially contain double bonds in the main chain, such as metal ion crosslinked ethylene-acrylic acid copolymers and polyisobutylene, ethylene-propylene-nonconjugated diene polymers It also includes copolymers having a small amount, usually 3% by weight or less, of unsaturated bonds in the main chain, such as isobutylene-isoprene copolymers. Polymers having more than 3% by weight of unsaturated bonds in the main chain are not used because their weather resistance decreases. Next, 1,2-polybutadiene, which is used as a second component in the composition of the present invention and does not contain an unsaturated bond in its main chain and has an unsaturated group in its side chain, can adhere without impairing the weather resistance of the composition. It is blended with the first component for the purpose of improving properties. As mentioned above, the second component does not contain unsaturated bonds in its main chain, so it has fairly good ozone deterioration resistance, and since it has unsaturated groups in its side chains, it can be surface-treated to improve adhesion. It is possible. Other desirable conditions for the second component are that it has good compatibility with the weather-resistant polymer and excellent mechanical properties. For this reason, as the second component,
1,2-polybutadiene, especially syndiotactic 1,2 which has an internal crystalline region and has high tensile strength.
-Polybutadiene is preferably used. The second component does not contribute to improving adhesion unless it is added in an amount of at least 20% by weight, where the sum of the weather-resistant polymer and the second component is 100. In order to improve adhesion, it is preferable to have a larger amount of the second component, and the effect is particularly noticeable when it is 30% by weight or more. This is because when a certain amount or more of the second component is added, unsaturated groups in the side chains of the second component appear on the surface of the blend in an amount sufficient for adhesion. On the other hand, if the amount of the second component is too large, the hardness of the composition will increase, flexibility will be lost, and deterioration due to ultraviolet light will become noticeable. Added. In order to further improve adhesive performance, the surface of the sheet formed by blending the weather-resistant polymer and the second component must be treated with a treatment agent, that is, a halogen molecule or a pseudohalogen compound (halogenoid). The halogen molecules used in the present invention include chlorine, bromine, iodine, and their 0.1 to
In addition to a 20% concentration aqueous solution or organic solvent solution, it includes a compound that generates halogen molecules in the presence of an acid, such as an aqueous solution of hypochlorous acid or hypobromous acid. Examples of pseudohalogen compounds (halogenoids) include halogenated isocyanates, N-monohaloalkyl urethanes, N,N-dihaloalkyl urethanes, N,N-dihaloallylsulfonamides, sulfur halides, sulfenyl halides, and halomethyl Ether, thiocyanogen, azide iodide, azide bromide, iodine chloride, iodine bromide, trichloroacetate iodide, acetate bromide, iodine nitrate, alkyl hypohalide, alkylthionyl chloride, allylthionyl chloride, nitrosyl chloride , nitrosyl bromide, halogenated isocyanuric acid, halogenated methylhydantoin, and the like. Among the above-mentioned processing agents, pseudohalogen compounds, especially halogenated isocyanates, N,N-dihaloalkyl urethanes, N,N-dihaloallylsulfonamides, alkyl hypohalides, and halogen Preferred are halogenated isocyanuric acid and halogenated methylhydantoin. Specifically, iodized isocyanate, N,N
-dichloroethyl urethane, N,N-dibromoethyl urethane, N,N-dichloropropylurethane, N,N-dibromopropylurethane, N,N
-dichlorobenzyl urethane, N,N-dibromobenzyl urethane, N,N-dichlorotoluenesulfonamide, N,N-dibromotoluenesulfonamide, tertiary butylhypochloride, trichloroisocyanuric acid, dichloroisocyanuric acid, dibromodimethylhydantoin, Compounds such as dichloromethylhydantoin. The above pseudohalogen compounds (halogenoids) must be dissolved in an appropriate solvent during actual processing.
It is used in concentrations of 0.1 to 20% by weight, preferably 1 to 15% by weight. Specific examples of solvents when the above treatment agent in the present invention is used as an organic solvent solution include carbon tetrachloride, chloroform, halogenated hydrocarbons such as dichloromethane, benzene, nitrobenzene, halogenated benzene, toluene, aromatic hydrocarbons such as xylene, etc. Hydrocarbons, chain or cyclic ethers such as dimethyl ether, diethyl ether, tetrahydrofuran (THF), and dioxane, esters such as ethyl acetate, aliphatic hydrocarbons such as pentane, hexane, heptane, octane, and cyclohexane,
Examples include ketones such as acetone, cyclohexanone, and methyl ethyl ketone (MEK); alcohols such as ethanol, ethylene glycol, and tertiary butyl alcohol; among others, tetrahydrofuran (THF), dioxane, acetone, benzene, toluene, and tetrachloride. Carbon, chloroform, methyl ethyl ketone (MEK), ethyl acetate, and ethanol are preferably used. The method of treating the sheet with the treatment agent is as follows:
Any industrial means capable of bringing the treatment agent into contact with the sheet surface can be employed, such as application with a brush or brush, spraying, or dipping. The surface of the sheet of the present invention treated with the above-mentioned treatment agent maintains a smooth surface and is indistinguishable from the sheet before treatment in appearance. The performance of the composition also remains unchanged before and after treatment. Adhesion to this treated sheet does not deteriorate even after one year or more after treatment. Further, in a preferred embodiment, the adhesive performance is better preserved by covering and protecting the treated sheet surface with a film, gummed tape, etc. to prevent staining. It is of course possible to incorporate fillers such as carbon black, silica, calcium carbonate, calcium silicate, and lignin, and softeners such as mineral oil, vegetable oil, and synthetic plasticizers into the composition. Further, if necessary, a vulcanizing agent such as sulfur, peroxide, quinoid, vulcanizing aid, etc. may be added to the composition, and the sheet may be formed by molding and vulcanizing, and then subjected to the above-mentioned surface treatment. Furthermore, the composition of the present invention may include a metal,
It is also possible to use a core material such as organic fiber or glass fiber, or a reinforcing material embedded therein. The sheet made of the weather-resistant polymer and the second component obtained by the surface treatment of the present invention has significantly improved adhesion without impairing the properties of conventional weather-resistant polymers, and can be used as an adherend. In addition to the sheet of the present invention, it can be used to connect with metal, rubber, plastic, wood, glass, etc., and in particular, a waterproof sheet,
Extremely effective for bonding joints of gaskets, belts, etc. In order to bond the sheet of the present invention and the adherend, polyurethane resin, epoxy resin, phenolaldehyde resin, polyhydric phenolaldehyde resin,
This is done by interposing nitrile rubber cement or the like on the adhesion surface and compressing it. The present invention will be explained in more detail below using examples. Example 1 As shown in Table 1 below, various amounts of syndiotactic 1 were added to ethylene-propylene-ethylidene norbornene copolymer (manufactured by Japan Synthetic Rubber Co., Ltd., JSREP33, iodine value 26, hereinafter referred to as EPDM). ,2-
Polybutadiene (Japan Synthetic Rubber, JSR
The physical properties and adhesive performance of a vulcanized rubber blended with RB820 (hereinafter referred to as PB) were evaluated. The basic composition is
For a total of 100 parts by weight of EPDM and PB, HAF Black 50, process oil 5, stearic acid 2, N
-isopropyl-N'-phenyl-p-phenylenediamine 1, paraffin wax 1, rosin 2 as a tackifier, zinc white 5, sulfur 2, N
-oxydiethylene-2-benzothiazolesulfenamide 1 part by weight, and the vulcanization conditions were 160
â for 20 minutes. Adhesion was evaluated as follows. Prepare two vulcanized rubber sheets 60 mm wide x 150 mm long x 2 mm thick, and apply an acetone solution containing 5% by weight N,N'-dichloro-p-toluenesulfonamide to the adhesive surface with a brush. I processed it. Add 100 parts of Adiprene L-213 (manufactured by DuPont, -NCO content 9.4%) as an adhesive to the treated surface, and add MOCA (3,3'-dichloro-4,4'-diaminodiphenylmethane, Dupont) as a hardening agent. (manufactured by S.A.) was dissolved in 125 g of acetone and mixed to make an adhesive.
This urethane solution was applied before the vulcanized rubber treatment, and after drying, the two rubber sheets were bonded together using a pressure roller, left at room temperature for 24 hours, and then punched out using an inch cutter to obtain an adhesive test piece A. Separately, a sheet of thermoplastic urethane resin (DN4818, manufactured by Nippon Polyurethane) with a thickness of 1 mm was sandwiched between two vulcanized rubber sheets whose surface had been treated in the same manner, and the sheet was pressed with an iron at 200°C for 40 seconds. , and the melt-adhesive pieces were similarly punched out using an inch cutter B to obtain an adhesive test piece B. Each test piece was subjected to a T-peel test using a tensile tester at a speed of 50 mm/min. The results obtained are shown in the attached drawings. In the drawings, curve 1 shows the results for test piece A, and curve 2 shows the results for test piece B. We also investigated the weather resistance of vulcanized rubber. In the ozone deterioration resistance test, the size of the vulcanized rubber was 20 mm in width and 70 mm in length.
mm, 2 mm thick sheet was stretched by 40% and the temperature was 40
The occurrence of cracks was investigated after deterioration for 168 hours at â and ozone concentration of 90 ppHm. In addition, in the ultraviolet ray deterioration test, vulcanized rubber (thickness 2 mm) was punched out with a JIS No. 3 dumbbell, the test piece was placed under a 400 W mercury lamp at a distance of 15 cm (approximately 19,000 ÎŒW), and after being irradiated with ultraviolet rays for 8 hours, the tensile speed was set at 30 mm. The rate of decrease was calculated by comparing it with the first one. The above test results are also listed in Table 1 below.
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ãšèšãïŒã«çš®ã
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0.5åéééšã§ãããå ç¡«æéã¯160âã§20åéã§
ãã€ããå ç¡«ç©ã®ç©æ§ã¯åŒåŒµãç©æ§ããã³èãªãŸ
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ïŒééïŒ
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ã«ãã³ã¢ãããå«ãã¢ã»ãã³æº¶æ¶²ãå¡åžãã衚é¢
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213ïŒMOCAïŒ100ïŒ25ïŒã®ã¢ã»ãã³æº¶æ¶²ã®æ¥ç
å€ãå¡åžããïŒæã貌ãåãå®€æž©ã§æŸçœ®ããŠç¡¬å
ããããã®ã詊éšçãšããã詊éšçµæã第ïŒè¡š
ã«ç€ºãã[Table] Example 2 As shown in Table 2 below, isoprene-isoptylene rubber (IIR-268 manufactured by Nippon Synthetic Rubber, hereinafter referred to as IIR)
The physical properties and adhesive performance of vulcanized rubber blended with various amounts of PB were evaluated. The basic composition is based on the total amount of IIR and PB of 100 parts by weight.
HAF black 50, process oil 5, stearic acid 2, N-isopropyl-N'-phenyl-p
-Phenylenediamine 1, paraffin wax 1, rosin 2, zinc white 5, sulfur 2, N-oxyethylene-2-benzothiazolesulfenamide 1, tetramethylenethiuram monosulfide
0.5 parts by weight each, and the vulcanization time was 20 minutes at 160°C. The physical properties of the vulcanizate were evaluated for tensile properties and ozone deterioration resistance. For adhesion evaluation, as in Example 1, an acetone solution containing 5% by weight N,N'-dichloro-p-toluenesulfonamide was applied to the vulcanized surface, and after surface treatment, 50% by weight of N,N'-dichloro-p-toluenesulfonamide was applied to the vulcanized surface. Adiprene L-
Test piece C was prepared by applying an adhesive of an acetone solution of 213/MOCA (100/25), bonding the two sheets together, and leaving them at room temperature to harden. The test results are shown in Table 2.
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第ïŒè¡šã«ç€ºãããã«ãäœå¯åºŠããªãšãã¬ã³ïŒãŠ
ã«ãã³MS30ãäžè±æ²¹å補ã以äžLDâPEãšèš
ãïŒãšçš®ã
ã®éã®PBã髿ž©ïŒ120âïŒããŒã«ã§æ··
åãã¬ã³ããã150âã®ãã¬ã¹ã§æº¶èæåœ¢ããã·
ãŒãã®ç©æ§åã³æ¥çæ§ãè©äŸ¡ãããæ¥çæ¹æ³ã¯å®
æœäŸïŒãšåæ§ã«è¡ããåŸã詊éšçããšããã詊
éšçµæã第ïŒè¡šã«äœµèšããã[Table] Example 3 As shown in Table 3, low density polyethylene (Yukalon MS30, manufactured by Mitsubishi Yuka, hereinafter referred to as LD-PE) and various amounts of PB were mixed and blended using a high temperature (120°C) roll. The physical properties and adhesive properties of sheets melt-molded in a press at 150°C were evaluated. The adhesion method was carried out in the same manner as in Example 1, and the obtained test piece was designated as D. The test results are also listed in Table 3.
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žå
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åäœã®éå±ã€ãªã³æ¶æ©ç©ã§ãããµãŒãªã³1555
ïŒNaã€ãªã³ã¿ã€ããäžäºããªã±ãã«ã«è£œã以äžãµ
ãŒãªã³ãšèšãïŒãšçš®ã
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䟡ãããæ¥çæ¹æ³ã¯å®æœäŸïŒãšåæ§ã«è¡ããåŸã
詊æã詊éšçãšããã詊éšçµæã第ïŒè¡šã«ç€º
ãã[Table] Example 4 As shown in Table 4, Surlyn 1555 is a metal ion crosslinked product of ethylene and acrylic acid copolymer.
(Na ion type, made by Mitsui Polychemicals, hereinafter referred to as Surlyn) and various amounts of PB were mixed in a high temperature roll and melt-formed in a press at a temperature of 150°C. The physical properties and adhesive properties of the sheet were the same as in Example 1. It was evaluated as follows. The adhesion method was carried out in the same manner as in Example 1, and the obtained sample was designated as Test Piece E. The test results are shown in Table 4.
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EPDMãšPBããã¬ã³ãããå ç¡«ãŽã ã·ãŒããš
éå±ïŒéçïŒã®æ¥çãè¡ã€ãã宿œäŸïŒã®å®éšçª
å·1dïŒEPDHïŒPBïŒ70ïŒ30ïŒã§è£œäœããå ç¡«ã·
ãŒããïŒééïŒ
ã®DCTSã®ã¢ã»ãã³æº¶æ¶²ã§è¡šé¢åŠ
çãè¡ã€ãã
äžæ¹éïŒSS41ïŒè¡šé¢ãã·ãšãããã©ã¹ãåŠç
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ãŠãŒãªã³ã±ãã«ã«ç€Ÿè£œïŒãå·æ¯å¡ãããã
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ïŒ100ïŒ25ïŒã®50ééïŒ
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50mmïŒç§ã§180°å¥é¢ãè¡ããæ¥çåãè©äŸ¡ãã
çµæã75KgïŒ25mmã®æ¥çåã§å ç¡«ãŽã ã®åéç Žå£
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ãã§ä¿è·ãããéå±ã®è€åäœãåŸãããã[Table] Example 5 A vulcanized rubber sheet made of a blend of EPDM and PB was bonded to a metal (iron piece). The vulcanized sheet produced in Experiment No. 1d (EPDH/PB=70/30) of Example 1 was surface-treated with a 5% by weight DCTS acetone solution. On the other hand, after the iron (SS41) surface was subjected to shotplast treatment, it was cleaned with acetone, and then Chemlock 218 (manufactured by Huurin Chemical Co., USA), which is an adhesive between metal and cast urethane, was applied with a brush. Adiprene L-213/MOCA as adhesive
(100/25) was applied with a brush to the treated vulcanized rubber and metal surfaces using a 50% by weight acetone solution.
After the solvent had evaporated, the two pieces were pasted together and fixed with cellophane tape, and left at room temperature for 48 hours to cure and bond. The adhesive piece was pulled at the same speed as in Example 1.
Peeling was performed at 180° at 50 mm/sec and the adhesive strength was evaluated. As a result, cohesive failure of the vulcanized rubber occurred at an adhesive strength of 75 kg/25 mm. As a result, a metal composite protected by a vulcanized sheet with excellent weather resistance was obtained.
æ·»ä»å³é¢ã¯å®æœäŸïŒã®è©Šéšçããã³ïŒ¢ã®
EPDMïŒPBãã¬ã³ãæ¯çãšå¥é¢åãšã®é¢ä¿ã瀺
ãæ²ç·å³ã§ããã
The attached drawings show test pieces A and B of Example 1.
It is a curve diagram showing the relationship between EPDM/PB blend ratio and peeling force.
Claims (1)
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é æ§ããªããŒã·ãŒãã ïŒ èåæ§ããªããŒãšç¬¬äºæåãé鿝ã§70ïŒ30
ã30ïŒ70ã®ç¯å²ã«ããç¹èš±è«æ±ã®ç¯å²ç¬¬ïŒé ã第
ïŒé ãŸãã¯ç¬¬ïŒé èšèŒã®æ¥çæ§è¯å¥œãªèåæ§ããª
ããŒã·ãŒãã ïŒ ç¬¬äºæåãã·ã³ãžãªã¿ã¯ãã€ãã¯ïŒïŒïŒâã
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æ§ããªããŒã·ãŒãã[Claims] 1. A weather-resistant polymer and a second component, 1,2-polybutadiene resin, are essential components, and the weight ratio of the weather-resistant polymer and the second component is in the range of 80:20 to 10:90. 1. A weather-resistant polymer sheet with good adhesion, characterized in that the surface of the sheet molded from a composition comprising the above-mentioned composition is treated with a halogen molecule or a pseudohalogen compound. 2. The weather-resistant polymer sheet with good adhesion according to claim 1, wherein the weather-resistant polymer does not contain unsaturated bonds in its main chain or has 3% by weight or less of unsaturated bonds. 3 The weather-resistant polymer is polyethylene, polypropylene, ethylene-vinyl acetate copolymer, ethylene-propylene copolymer, ethylene-acrylic acid copolymer, ethylene-acrylic acid copolymer, metal ion of ethylene-acrylic acid copolymer A crosslinked product having good adhesive properties and durability according to claim 1 or 2, which is at least one selected from crosslinked products, polyisobutylene, ethylene-propylene-nonconjugated diene copolymers, and isobutylene-isoprene copolymers. Polymer sheet. 4 Weather-resistant polymer and second component in weight ratio of 70:30
A weather-resistant polymer sheet with good adhesion according to claim 1, 2 or 3, which has a ratio of 1 to 30:70. 5 Claims 1 to 4 in which the second component is a syndiotactic 1,2-polybutadiene resin
A weather-resistant polymer sheet with good adhesion as described in any one of the above items.
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP6136578A JPS54153854A (en) | 1978-05-23 | 1978-05-23 | Weather-resistant polymer composition having high adhesivity |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP6136578A JPS54153854A (en) | 1978-05-23 | 1978-05-23 | Weather-resistant polymer composition having high adhesivity |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| JPS54153854A JPS54153854A (en) | 1979-12-04 |
| JPS6234781B2 true JPS6234781B2 (en) | 1987-07-29 |
Family
ID=13169054
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP6136578A Granted JPS54153854A (en) | 1978-05-23 | 1978-05-23 | Weather-resistant polymer composition having high adhesivity |
Country Status (1)
| Country | Link |
|---|---|
| JP (1) | JPS54153854A (en) |
Families Citing this family (4)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US4371662A (en) | 1980-09-01 | 1983-02-01 | Idemitsu Petrochemical Co., Ltd. | Three-component resin compositions having improved coating properties |
| JPS5847048A (en) * | 1981-09-14 | 1983-03-18 | Takiron Co Ltd | Cushioning material for use in transportation |
| US5153262A (en) * | 1991-03-29 | 1992-10-06 | The Goodyear Tire & Rubber Company | Controlled morphology barrier elastomers made from blends of syndiotactic 1,2-polybutadiene and ethylene-vinyl acetate-vinyl alcohol terpolymers |
| US5091467A (en) * | 1991-03-29 | 1992-02-25 | The Goodyear Tire & Rubber Company | Controlled morphology barrier elastomers made from blends of syndiotactic 1,2-polybutadiene and ethylene-vinyl acetate-vinyl alcohol terpolymers |
-
1978
- 1978-05-23 JP JP6136578A patent/JPS54153854A/en active Granted
Also Published As
| Publication number | Publication date |
|---|---|
| JPS54153854A (en) | 1979-12-04 |
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