KR960002983B1 - 내열성 공중합체 조성물 - Google Patents
내열성 공중합체 조성물 Download PDFInfo
- Publication number
- KR960002983B1 KR960002983B1 KR1019870012752A KR870012752A KR960002983B1 KR 960002983 B1 KR960002983 B1 KR 960002983B1 KR 1019870012752 A KR1019870012752 A KR 1019870012752A KR 870012752 A KR870012752 A KR 870012752A KR 960002983 B1 KR960002983 B1 KR 960002983B1
- Authority
- KR
- South Korea
- Prior art keywords
- copolymer
- monomer
- parts
- unsaturated nitrile
- weight
- Prior art date
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- 229920001577 copolymer Polymers 0.000 title claims description 189
- 239000000203 mixture Substances 0.000 title claims description 59
- 239000000178 monomer Substances 0.000 claims description 136
- 229920001971 elastomer Polymers 0.000 claims description 50
- 239000000806 elastomer Substances 0.000 claims description 49
- 150000002825 nitriles Chemical class 0.000 claims description 46
- PEEHTFAAVSWFBL-UHFFFAOYSA-N Maleimide Chemical compound O=C1NC(=O)C=C1 PEEHTFAAVSWFBL-UHFFFAOYSA-N 0.000 claims description 25
- 229920000642 polymer Polymers 0.000 claims description 13
- 229920002554 vinyl polymer Polymers 0.000 claims description 13
- 229920005992 thermoplastic resin Polymers 0.000 claims description 6
- 238000007334 copolymerization reaction Methods 0.000 claims description 5
- BSSNZUFKXJJCBG-UPHRSURJSA-N (z)-but-2-enediamide Chemical compound NC(=O)\C=C/C(N)=O BSSNZUFKXJJCBG-UPHRSURJSA-N 0.000 claims description 3
- 229920002725 thermoplastic elastomer Polymers 0.000 claims description 3
- 229920001198 elastomeric copolymer Polymers 0.000 claims 1
- PPBRXRYQALVLMV-UHFFFAOYSA-N Styrene Chemical compound C=CC1=CC=CC=C1 PPBRXRYQALVLMV-UHFFFAOYSA-N 0.000 description 22
- 239000004816 latex Substances 0.000 description 21
- 229920000126 latex Polymers 0.000 description 21
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Chemical compound O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 18
- IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 description 17
- NLHHRLWOUZZQLW-UHFFFAOYSA-N Acrylonitrile Chemical compound C=CC#N NLHHRLWOUZZQLW-UHFFFAOYSA-N 0.000 description 16
- -1 methyl Chemical class 0.000 description 16
- 239000000243 solution Substances 0.000 description 13
- ZMXDDKWLCZADIW-UHFFFAOYSA-N N,N-Dimethylformamide Chemical compound CN(C)C=O ZMXDDKWLCZADIW-UHFFFAOYSA-N 0.000 description 12
- 238000006116 polymerization reaction Methods 0.000 description 11
- 239000007787 solid Substances 0.000 description 11
- 239000007864 aqueous solution Substances 0.000 description 10
- 229910052757 nitrogen Inorganic materials 0.000 description 10
- YAJYJWXEWKRTPO-UHFFFAOYSA-N 2,3,3,4,4,5-hexamethylhexane-2-thiol Chemical compound CC(C)C(C)(C)C(C)(C)C(C)(C)S YAJYJWXEWKRTPO-UHFFFAOYSA-N 0.000 description 9
- OKKJLVBELUTLKV-UHFFFAOYSA-N Methanol Chemical compound OC OKKJLVBELUTLKV-UHFFFAOYSA-N 0.000 description 9
- 239000008367 deionised water Substances 0.000 description 8
- 229910021641 deionized water Inorganic materials 0.000 description 8
- 238000002360 preparation method Methods 0.000 description 8
- HIDBROSJWZYGSZ-UHFFFAOYSA-N 1-phenylpyrrole-2,5-dione Chemical compound O=C1C=CC(=O)N1C1=CC=CC=C1 HIDBROSJWZYGSZ-UHFFFAOYSA-N 0.000 description 7
- 238000001816 cooling Methods 0.000 description 6
- 238000000465 moulding Methods 0.000 description 6
- 239000011347 resin Substances 0.000 description 6
- 229920005989 resin Polymers 0.000 description 6
- DGAQECJNVWCQMB-PUAWFVPOSA-M Ilexoside XXIX Chemical compound C[C@@H]1CC[C@@]2(CC[C@@]3(C(=CC[C@H]4[C@]3(CC[C@@H]5[C@@]4(CC[C@@H](C5(C)C)OS(=O)(=O)[O-])C)C)[C@@H]2[C@]1(C)O)C)C(=O)O[C@H]6[C@@H]([C@H]([C@@H]([C@H](O6)CO)O)O)O.[Na+] DGAQECJNVWCQMB-PUAWFVPOSA-M 0.000 description 5
- XYLMUPLGERFSHI-UHFFFAOYSA-N alpha-Methylstyrene Chemical compound CC(=C)C1=CC=CC=C1 XYLMUPLGERFSHI-UHFFFAOYSA-N 0.000 description 5
- 229920001400 block copolymer Polymers 0.000 description 5
- 238000000034 method Methods 0.000 description 5
- 239000002245 particle Substances 0.000 description 5
- 239000008188 pellet Substances 0.000 description 5
- SCUZVMOVTVSBLE-UHFFFAOYSA-N prop-2-enenitrile;styrene Chemical compound C=CC#N.C=CC1=CC=CC=C1 SCUZVMOVTVSBLE-UHFFFAOYSA-N 0.000 description 5
- 239000011734 sodium Substances 0.000 description 5
- 229910052708 sodium Inorganic materials 0.000 description 5
- 238000003756 stirring Methods 0.000 description 5
- PAYRUJLWNCNPSJ-UHFFFAOYSA-N Aniline Chemical compound NC1=CC=CC=C1 PAYRUJLWNCNPSJ-UHFFFAOYSA-N 0.000 description 4
- CSNNHWWHGAXBCP-UHFFFAOYSA-L Magnesium sulfate Chemical compound [Mg+2].[O-][S+2]([O-])([O-])[O-] CSNNHWWHGAXBCP-UHFFFAOYSA-L 0.000 description 4
- MTAZNLWOLGHBHU-UHFFFAOYSA-N butadiene-styrene rubber Chemical compound C=CC=C.C=CC1=CC=CC=C1 MTAZNLWOLGHBHU-UHFFFAOYSA-N 0.000 description 4
- 229920000578 graft copolymer Polymers 0.000 description 4
- 239000004417 polycarbonate Substances 0.000 description 4
- 229920005604 random copolymer Polymers 0.000 description 4
- 239000005060 rubber Substances 0.000 description 4
- 238000010557 suspension polymerization reaction Methods 0.000 description 4
- GETQZCLCWQTVFV-UHFFFAOYSA-N trimethylamine Chemical compound CN(C)C GETQZCLCWQTVFV-UHFFFAOYSA-N 0.000 description 4
- VXNZUUAINFGPBY-UHFFFAOYSA-N 1-Butene Chemical compound CCC=C VXNZUUAINFGPBY-UHFFFAOYSA-N 0.000 description 3
- NIXOWILDQLNWCW-UHFFFAOYSA-M Acrylate Chemical compound [O-]C(=O)C=C NIXOWILDQLNWCW-UHFFFAOYSA-M 0.000 description 3
- VGGSQFUCUMXWEO-UHFFFAOYSA-N Ethene Chemical compound C=C VGGSQFUCUMXWEO-UHFFFAOYSA-N 0.000 description 3
- 239000005977 Ethylene Substances 0.000 description 3
- WQZGKKKJIJFFOK-GASJEMHNSA-N Glucose Natural products OC[C@H]1OC(O)[C@H](O)[C@@H](O)[C@@H]1O WQZGKKKJIJFFOK-GASJEMHNSA-N 0.000 description 3
- 239000004952 Polyamide Substances 0.000 description 3
- 239000005062 Polybutadiene Substances 0.000 description 3
- HEMHJVSKTPXQMS-UHFFFAOYSA-M Sodium hydroxide Chemical compound [OH-].[Na+] HEMHJVSKTPXQMS-UHFFFAOYSA-M 0.000 description 3
- DBMJMQXJHONAFJ-UHFFFAOYSA-M Sodium laurylsulphate Chemical compound [Na+].CCCCCCCCCCCCOS([O-])(=O)=O DBMJMQXJHONAFJ-UHFFFAOYSA-M 0.000 description 3
- 150000001252 acrylic acid derivatives Chemical class 0.000 description 3
- 229920001893 acrylonitrile styrene Polymers 0.000 description 3
- 125000000484 butyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 description 3
- 238000006243 chemical reaction Methods 0.000 description 3
- 239000008121 dextrose Substances 0.000 description 3
- 239000003995 emulsifying agent Substances 0.000 description 3
- 125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 description 3
- 230000009477 glass transition Effects 0.000 description 3
- 125000003055 glycidyl group Chemical group C(C1CO1)* 0.000 description 3
- VOZRXNHHFUQHIL-UHFFFAOYSA-N glycidyl methacrylate Chemical compound CC(=C)C(=O)OCC1CO1 VOZRXNHHFUQHIL-UHFFFAOYSA-N 0.000 description 3
- FPYJFEHAWHCUMM-UHFFFAOYSA-N maleic anhydride Chemical compound O=C1OC(=O)C=C1 FPYJFEHAWHCUMM-UHFFFAOYSA-N 0.000 description 3
- 238000004519 manufacturing process Methods 0.000 description 3
- 229910052751 metal Inorganic materials 0.000 description 3
- 239000002184 metal Substances 0.000 description 3
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 description 3
- QJGQUHMNIGDVPM-UHFFFAOYSA-N nitrogen group Chemical group [N] QJGQUHMNIGDVPM-UHFFFAOYSA-N 0.000 description 3
- 229920002647 polyamide Polymers 0.000 description 3
- 229920002857 polybutadiene Polymers 0.000 description 3
- 229920000515 polycarbonate Polymers 0.000 description 3
- USHAGKDGDHPEEY-UHFFFAOYSA-L potassium persulfate Chemical compound [K+].[K+].[O-]S(=O)(=O)OOS([O-])(=O)=O USHAGKDGDHPEEY-UHFFFAOYSA-L 0.000 description 3
- 125000001436 propyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])[H] 0.000 description 3
- 239000002002 slurry Substances 0.000 description 3
- 235000019333 sodium laurylsulphate Nutrition 0.000 description 3
- 239000000126 substance Substances 0.000 description 3
- IANQTJSKSUMEQM-UHFFFAOYSA-N 1-benzofuran Chemical compound C1=CC=C2OC=CC2=C1 IANQTJSKSUMEQM-UHFFFAOYSA-N 0.000 description 2
- YBYIRNPNPLQARY-UHFFFAOYSA-N 1H-indene Chemical compound C1=CC=C2CC=CC2=C1 YBYIRNPNPLQARY-UHFFFAOYSA-N 0.000 description 2
- FRIBMENBGGCKPD-UHFFFAOYSA-N 3-(2,3-dimethoxyphenyl)prop-2-enal Chemical compound COC1=CC=CC(C=CC=O)=C1OC FRIBMENBGGCKPD-UHFFFAOYSA-N 0.000 description 2
- CSCPPACGZOOCGX-UHFFFAOYSA-N Acetone Chemical compound CC(C)=O CSCPPACGZOOCGX-UHFFFAOYSA-N 0.000 description 2
- QGZKDVFQNNGYKY-UHFFFAOYSA-N Ammonia Chemical compound N QGZKDVFQNNGYKY-UHFFFAOYSA-N 0.000 description 2
- 239000004342 Benzoyl peroxide Substances 0.000 description 2
- OMPJBNCRMGITSC-UHFFFAOYSA-N Benzoylperoxide Chemical compound C=1C=CC=CC=1C(=O)OOC(=O)C1=CC=CC=C1 OMPJBNCRMGITSC-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
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 description 2
- 229920000181 Ethylene propylene rubber Polymers 0.000 description 2
- QIGBRXMKCJKVMJ-UHFFFAOYSA-N Hydroquinone Chemical compound OC1=CC=C(O)C=C1 QIGBRXMKCJKVMJ-UHFFFAOYSA-N 0.000 description 2
- YIVJZNGAASQVEM-UHFFFAOYSA-N Lauroyl peroxide Chemical compound CCCCCCCCCCCC(=O)OOC(=O)CCCCCCCCCCC YIVJZNGAASQVEM-UHFFFAOYSA-N 0.000 description 2
- VVQNEPGJFQJSBK-UHFFFAOYSA-N Methyl methacrylate Chemical compound COC(=O)C(C)=C VVQNEPGJFQJSBK-UHFFFAOYSA-N 0.000 description 2
- GYCMBHHDWRMZGG-UHFFFAOYSA-N Methylacrylonitrile Chemical compound CC(=C)C#N GYCMBHHDWRMZGG-UHFFFAOYSA-N 0.000 description 2
- 229920000459 Nitrile rubber Polymers 0.000 description 2
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 description 2
- 239000002174 Styrene-butadiene Substances 0.000 description 2
- MCMNRKCIXSYSNV-UHFFFAOYSA-N Zirconium dioxide Chemical compound O=[Zr]=O MCMNRKCIXSYSNV-UHFFFAOYSA-N 0.000 description 2
- 229920000800 acrylic rubber Polymers 0.000 description 2
- 229920000122 acrylonitrile butadiene styrene Polymers 0.000 description 2
- 239000000654 additive Substances 0.000 description 2
- 239000011324 bead Substances 0.000 description 2
- 235000019400 benzoyl peroxide Nutrition 0.000 description 2
- 238000012662 bulk polymerization Methods 0.000 description 2
- 230000000052 comparative effect Effects 0.000 description 2
- 229920003244 diene elastomer Polymers 0.000 description 2
- VVSMKOFFCAJOSC-UHFFFAOYSA-L disodium;dodecylbenzene;sulfate Chemical compound [Na+].[Na+].[O-]S([O-])(=O)=O.CCCCCCCCCCCCC1=CC=CC=C1 VVSMKOFFCAJOSC-UHFFFAOYSA-L 0.000 description 2
- 238000007720 emulsion polymerization reaction Methods 0.000 description 2
- 150000002148 esters Chemical class 0.000 description 2
- 239000005038 ethylene vinyl acetate Substances 0.000 description 2
- 238000010528 free radical solution polymerization reaction Methods 0.000 description 2
- 239000000314 lubricant Substances 0.000 description 2
- 229910052943 magnesium sulfate Inorganic materials 0.000 description 2
- 235000019341 magnesium sulphate Nutrition 0.000 description 2
- 230000000704 physical effect Effects 0.000 description 2
- 229920001084 poly(chloroprene) Polymers 0.000 description 2
- 229920001200 poly(ethylene-vinyl acetate) Polymers 0.000 description 2
- 229920002037 poly(vinyl butyral) polymer Polymers 0.000 description 2
- 229920000058 polyacrylate Polymers 0.000 description 2
- 229920000728 polyester Polymers 0.000 description 2
- 230000000379 polymerizing effect Effects 0.000 description 2
- 239000000843 powder Substances 0.000 description 2
- FQENQNTWSFEDLI-UHFFFAOYSA-J sodium diphosphate Chemical compound [Na+].[Na+].[Na+].[Na+].[O-]P([O-])(=O)OP([O-])([O-])=O FQENQNTWSFEDLI-UHFFFAOYSA-J 0.000 description 2
- 229940048086 sodium pyrophosphate Drugs 0.000 description 2
- 239000002904 solvent Substances 0.000 description 2
- 229920000638 styrene acrylonitrile Polymers 0.000 description 2
- 239000011115 styrene butadiene Substances 0.000 description 2
- 229920003048 styrene butadiene rubber Polymers 0.000 description 2
- CIHOLLKRGTVIJN-UHFFFAOYSA-N tert‐butyl hydroperoxide Chemical compound CC(C)(C)OO CIHOLLKRGTVIJN-UHFFFAOYSA-N 0.000 description 2
- 235000019818 tetrasodium diphosphate Nutrition 0.000 description 2
- 239000001577 tetrasodium phosphonato phosphate Substances 0.000 description 2
- 229960000834 vinyl ether Drugs 0.000 description 2
- KYPOHTVBFVELTG-OWOJBTEDSA-N (e)-but-2-enedinitrile Chemical compound N#C\C=C\C#N KYPOHTVBFVELTG-OWOJBTEDSA-N 0.000 description 1
- KYPOHTVBFVELTG-UPHRSURJSA-N (z)-but-2-enedinitrile Chemical compound N#C\C=C/C#N KYPOHTVBFVELTG-UPHRSURJSA-N 0.000 description 1
- NPPBRDURJSHSJE-UHFFFAOYSA-N 1,2-dibromo-4-ethenylbenzene Chemical compound BrC1=CC=C(C=C)C=C1Br NPPBRDURJSHSJE-UHFFFAOYSA-N 0.000 description 1
- BJQFWAQRPATHTR-UHFFFAOYSA-N 1,2-dichloro-4-ethenylbenzene Chemical compound ClC1=CC=C(C=C)C=C1Cl BJQFWAQRPATHTR-UHFFFAOYSA-N 0.000 description 1
- KWVKCGGJLLNVSC-UHFFFAOYSA-N 1,4-dibromo-2-ethenylbenzene Chemical compound BrC1=CC=C(Br)C(C=C)=C1 KWVKCGGJLLNVSC-UHFFFAOYSA-N 0.000 description 1
- IZMZREOTRMMCCB-UHFFFAOYSA-N 1,4-dichloro-2-ethenylbenzene Chemical compound ClC1=CC=C(Cl)C(C=C)=C1 IZMZREOTRMMCCB-UHFFFAOYSA-N 0.000 description 1
- MDBNEJWCBWGPAH-UHFFFAOYSA-N 1-(4-benzylphenyl)pyrrole-2,5-dione Chemical compound O=C1C=CC(=O)N1C(C=C1)=CC=C1CC1=CC=CC=C1 MDBNEJWCBWGPAH-UHFFFAOYSA-N 0.000 description 1
- VAYJAEOCYWSGBB-UHFFFAOYSA-N 1-(4-phenoxyphenyl)pyrrole-2,5-dione Chemical compound O=C1C=CC(=O)N1C(C=C1)=CC=C1OC1=CC=CC=C1 VAYJAEOCYWSGBB-UHFFFAOYSA-N 0.000 description 1
- SSZOCHFYWWVSAI-UHFFFAOYSA-N 1-bromo-2-ethenylbenzene Chemical compound BrC1=CC=CC=C1C=C SSZOCHFYWWVSAI-UHFFFAOYSA-N 0.000 description 1
- WGGLDBIZIQMEGH-UHFFFAOYSA-N 1-bromo-4-ethenylbenzene Chemical compound BrC1=CC=C(C=C)C=C1 WGGLDBIZIQMEGH-UHFFFAOYSA-N 0.000 description 1
- JNPCNDJVEUEFBO-UHFFFAOYSA-N 1-butylpyrrole-2,5-dione Chemical compound CCCCN1C(=O)C=CC1=O JNPCNDJVEUEFBO-UHFFFAOYSA-N 0.000 description 1
- KTZVZZJJVJQZHV-UHFFFAOYSA-N 1-chloro-4-ethenylbenzene Chemical compound ClC1=CC=C(C=C)C=C1 KTZVZZJJVJQZHV-UHFFFAOYSA-N 0.000 description 1
- XHAFIUUYXQFJEW-UHFFFAOYSA-N 1-chloroethenylbenzene Chemical compound ClC(=C)C1=CC=CC=C1 XHAFIUUYXQFJEW-UHFFFAOYSA-N 0.000 description 1
- BQTPKSBXMONSJI-UHFFFAOYSA-N 1-cyclohexylpyrrole-2,5-dione Chemical compound O=C1C=CC(=O)N1C1CCCCC1 BQTPKSBXMONSJI-UHFFFAOYSA-N 0.000 description 1
- SJLLJZNSZJHXQN-UHFFFAOYSA-N 1-dodecylpyrrole-2,5-dione Chemical compound CCCCCCCCCCCCN1C(=O)C=CC1=O SJLLJZNSZJHXQN-UHFFFAOYSA-N 0.000 description 1
- FBPVUBVZRPURIU-UHFFFAOYSA-N 1-hexylpyrrole-2,5-dione Chemical compound CCCCCCN1C(=O)C=CC1=O FBPVUBVZRPURIU-UHFFFAOYSA-N 0.000 description 1
- JTVXKQUORIWPAM-UHFFFAOYSA-N 1-naphthalen-1-yl-3-phenylpyrrole-2,5-dione Chemical compound O=C1N(C=2C3=CC=CC=C3C=CC=2)C(=O)C=C1C1=CC=CC=C1 JTVXKQUORIWPAM-UHFFFAOYSA-N 0.000 description 1
- KIKBJYQCJJXCBZ-UHFFFAOYSA-N 1-octylpyrrole-2,5-dione Chemical compound CCCCCCCCN1C(=O)C=CC1=O KIKBJYQCJJXCBZ-UHFFFAOYSA-N 0.000 description 1
- NQDOCLXQTQYUDH-UHFFFAOYSA-N 1-propan-2-ylpyrrole-2,5-dione Chemical compound CC(C)N1C(=O)C=CC1=O NQDOCLXQTQYUDH-UHFFFAOYSA-N 0.000 description 1
- GXURZKWLMYOCDX-UHFFFAOYSA-N 2,2-bis(hydroxymethyl)propane-1,3-diol;dihydroxyphosphanyl dihydrogen phosphite Chemical compound OP(O)OP(O)O.OCC(CO)(CO)CO GXURZKWLMYOCDX-UHFFFAOYSA-N 0.000 description 1
- 150000003923 2,5-pyrrolediones Chemical class 0.000 description 1
- OEPOKWHJYJXUGD-UHFFFAOYSA-N 2-(3-phenylmethoxyphenyl)-1,3-thiazole-4-carbaldehyde Chemical compound O=CC1=CSC(C=2C=C(OCC=3C=CC=CC=3)C=CC=2)=N1 OEPOKWHJYJXUGD-UHFFFAOYSA-N 0.000 description 1
- JCJIZBQZPSZIBI-UHFFFAOYSA-N 2-[2,6-di(propan-2-yl)phenyl]benzo[de]isoquinoline-1,3-dione Chemical compound CC(C)C1=CC=CC(C(C)C)=C1N(C1=O)C(=O)C2=C3C1=CC=CC3=CC=C2 JCJIZBQZPSZIBI-UHFFFAOYSA-N 0.000 description 1
- QSRJVOOOWGXUDY-UHFFFAOYSA-N 2-[2-[2-[3-(3-tert-butyl-4-hydroxy-5-methylphenyl)propanoyloxy]ethoxy]ethoxy]ethyl 3-(3-tert-butyl-4-hydroxy-5-methylphenyl)propanoate Chemical compound CC(C)(C)C1=C(O)C(C)=CC(CCC(=O)OCCOCCOCCOC(=O)CCC=2C=C(C(O)=C(C)C=2)C(C)(C)C)=C1 QSRJVOOOWGXUDY-UHFFFAOYSA-N 0.000 description 1
- 125000000022 2-aminoethyl group Chemical group [H]C([*])([H])C([H])([H])N([H])[H] 0.000 description 1
- ISRGONDNXBCDBM-UHFFFAOYSA-N 2-chlorostyrene Chemical compound ClC1=CC=CC=C1C=C ISRGONDNXBCDBM-UHFFFAOYSA-N 0.000 description 1
- ZNQVEEAIQZEUHB-UHFFFAOYSA-N 2-ethoxyethanol Chemical compound CCOCCO ZNQVEEAIQZEUHB-UHFFFAOYSA-N 0.000 description 1
- ANCUXNXTHQXICN-UHFFFAOYSA-N 2-prop-1-en-2-ylnaphthalene Chemical compound C1=CC=CC2=CC(C(=C)C)=CC=C21 ANCUXNXTHQXICN-UHFFFAOYSA-N 0.000 description 1
- KGIGUEBEKRSTEW-UHFFFAOYSA-N 2-vinylpyridine Chemical compound C=CC1=CC=CC=N1 KGIGUEBEKRSTEW-UHFFFAOYSA-N 0.000 description 1
- VNSHCVIITDMKAM-UHFFFAOYSA-N 3-(4-butylphenyl)pyrrole-2,5-dione Chemical compound C1=CC(CCCC)=CC=C1C1=CC(=O)NC1=O VNSHCVIITDMKAM-UHFFFAOYSA-N 0.000 description 1
- IJMBFOPCPHVSRS-UHFFFAOYSA-N 3-(4-chlorophenyl)pyrrole-2,5-dione Chemical compound C1=CC(Cl)=CC=C1C1=CC(=O)NC1=O IJMBFOPCPHVSRS-UHFFFAOYSA-N 0.000 description 1
- KYKRUDMJGYVFCD-UHFFFAOYSA-N 3-(4-ethylphenyl)pyrrole-2,5-dione Chemical compound C1=CC(CC)=CC=C1C1=CC(=O)NC1=O KYKRUDMJGYVFCD-UHFFFAOYSA-N 0.000 description 1
- SXPVZPQNFIDDPP-UHFFFAOYSA-N 3-(4-hydroxyphenyl)pyrrole-2,5-dione Chemical compound C1=CC(O)=CC=C1C1=CC(=O)NC1=O SXPVZPQNFIDDPP-UHFFFAOYSA-N 0.000 description 1
- LGXGCMJVZWBFSV-UHFFFAOYSA-N 3-(4-methoxyphenyl)pyrrole-2,5-dione Chemical compound C1=CC(OC)=CC=C1C1=CC(=O)NC1=O LGXGCMJVZWBFSV-UHFFFAOYSA-N 0.000 description 1
- UJNLRBKIVGGVIP-UHFFFAOYSA-N 3-(4-methylphenyl)pyrrole-2,5-dione Chemical compound C1=CC(C)=CC=C1C1=CC(=O)NC1=O UJNLRBKIVGGVIP-UHFFFAOYSA-N 0.000 description 1
- AYKYXWQEBUNJCN-UHFFFAOYSA-N 3-methylfuran-2,5-dione Chemical compound CC1=CC(=O)OC1=O AYKYXWQEBUNJCN-UHFFFAOYSA-N 0.000 description 1
- OFNISBHGPNMTMS-UHFFFAOYSA-N 3-methylideneoxolane-2,5-dione Chemical compound C=C1CC(=O)OC1=O OFNISBHGPNMTMS-UHFFFAOYSA-N 0.000 description 1
- PRXNTCCKSPNEFB-UHFFFAOYSA-N 4-(2,5-dioxopyrrol-1-yl)benzonitrile Chemical compound O=C1C=CC(=O)N1C1=CC=C(C#N)C=C1 PRXNTCCKSPNEFB-UHFFFAOYSA-N 0.000 description 1
- WIDLYFZFVAGYAJ-UHFFFAOYSA-N 4-(2,5-dioxopyrrol-3-yl)benzoic acid Chemical compound C1=CC(C(=O)O)=CC=C1C1=CC(=O)NC1=O WIDLYFZFVAGYAJ-UHFFFAOYSA-N 0.000 description 1
- JLBJTVDPSNHSKJ-UHFFFAOYSA-N 4-Methylstyrene Chemical compound CC1=CC=C(C=C)C=C1 JLBJTVDPSNHSKJ-UHFFFAOYSA-N 0.000 description 1
- WSSSPWUEQFSQQG-UHFFFAOYSA-N 4-methyl-1-pentene Chemical compound CC(C)CC=C WSSSPWUEQFSQQG-UHFFFAOYSA-N 0.000 description 1
- HRPVXLWXLXDGHG-UHFFFAOYSA-N Acrylamide Chemical compound NC(=O)C=C HRPVXLWXLXDGHG-UHFFFAOYSA-N 0.000 description 1
- 229910052582 BN Inorganic materials 0.000 description 1
- PZNSFCLAULLKQX-UHFFFAOYSA-N Boron nitride Chemical compound N#B PZNSFCLAULLKQX-UHFFFAOYSA-N 0.000 description 1
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- 238000000113 differential scanning calorimetry Methods 0.000 description 1
- NJLLQSBAHIKGKF-UHFFFAOYSA-N dipotassium dioxido(oxo)titanium Chemical compound [K+].[K+].[O-][Ti]([O-])=O NJLLQSBAHIKGKF-UHFFFAOYSA-N 0.000 description 1
- 125000003438 dodecyl group Chemical group [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])* 0.000 description 1
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- SURQXAFEQWPFPV-UHFFFAOYSA-L iron(2+) sulfate heptahydrate Chemical compound O.O.O.O.O.O.O.[Fe+2].[O-]S([O-])(=O)=O SURQXAFEQWPFPV-UHFFFAOYSA-L 0.000 description 1
- WVLDCUJMGWFHGE-UHFFFAOYSA-L iron(2+);sulfate;hexahydrate Chemical compound O.O.O.O.O.O.[Fe+2].[O-]S([O-])(=O)=O WVLDCUJMGWFHGE-UHFFFAOYSA-L 0.000 description 1
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- 239000004611 light stabiliser Substances 0.000 description 1
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- 238000002844 melting Methods 0.000 description 1
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- VNWKTOKETHGBQD-UHFFFAOYSA-N methane Chemical compound C VNWKTOKETHGBQD-UHFFFAOYSA-N 0.000 description 1
- IWVKTOUOPHGZRX-UHFFFAOYSA-N methyl 2-methylprop-2-enoate;2-methylprop-2-enoic acid Chemical compound CC(=C)C(O)=O.COC(=O)C(C)=C IWVKTOUOPHGZRX-UHFFFAOYSA-N 0.000 description 1
- OLTDMHPPKGCNIZ-UHFFFAOYSA-N methyl 2-methylprop-2-enoate;oxane-2,6-dione Chemical compound COC(=O)C(C)=C.O=C1CCCC(=O)O1 OLTDMHPPKGCNIZ-UHFFFAOYSA-N 0.000 description 1
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- SEEYREPSKCQBBF-UHFFFAOYSA-N n-methylmaleimide Chemical compound CN1C(=O)C=CC1=O SEEYREPSKCQBBF-UHFFFAOYSA-N 0.000 description 1
- KKFHAJHLJHVUDM-UHFFFAOYSA-N n-vinylcarbazole Chemical compound C1=CC=C2N(C=C)C3=CC=CC=C3C2=C1 KKFHAJHLJHVUDM-UHFFFAOYSA-N 0.000 description 1
- 229920003052 natural elastomer Polymers 0.000 description 1
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- 239000012766 organic filler Substances 0.000 description 1
- 239000011368 organic material Substances 0.000 description 1
- 239000001301 oxygen Substances 0.000 description 1
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- UCUUFSAXZMGPGH-UHFFFAOYSA-N penta-1,4-dien-3-one Chemical compound C=CC(=O)C=C UCUUFSAXZMGPGH-UHFFFAOYSA-N 0.000 description 1
- JRKICGRDRMAZLK-UHFFFAOYSA-L peroxydisulfate Chemical compound [O-]S(=O)(=O)OOS([O-])(=O)=O JRKICGRDRMAZLK-UHFFFAOYSA-L 0.000 description 1
- 239000004014 plasticizer Substances 0.000 description 1
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- 229920002493 poly(chlorotrifluoroethylene) Polymers 0.000 description 1
- 229920001643 poly(ether ketone) Polymers 0.000 description 1
- 229920003229 poly(methyl methacrylate) Polymers 0.000 description 1
- 229920002492 poly(sulfone) Polymers 0.000 description 1
- 229920002312 polyamide-imide Polymers 0.000 description 1
- 229920001748 polybutylene Polymers 0.000 description 1
- 239000005023 polychlorotrifluoroethylene (PCTFE) polymer Substances 0.000 description 1
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- 229920001601 polyetherimide Polymers 0.000 description 1
- 229920000573 polyethylene Polymers 0.000 description 1
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- 239000004926 polymethyl methacrylate Substances 0.000 description 1
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- 229920001955 polyphenylene ether Polymers 0.000 description 1
- 229920006380 polyphenylene oxide Polymers 0.000 description 1
- 229920000069 polyphenylene sulfide Polymers 0.000 description 1
- 229920001155 polypropylene Polymers 0.000 description 1
- 229920002223 polystyrene Polymers 0.000 description 1
- 239000004800 polyvinyl chloride Substances 0.000 description 1
- 229920000915 polyvinyl chloride Polymers 0.000 description 1
- 150000003141 primary amines Chemical class 0.000 description 1
- 239000000047 product Substances 0.000 description 1
- IPEHBUMCGVEMRF-UHFFFAOYSA-N pyrazinecarboxamide Chemical compound NC(=O)C1=CN=CC=N1 IPEHBUMCGVEMRF-UHFFFAOYSA-N 0.000 description 1
- 239000011342 resin composition Substances 0.000 description 1
- HBMJWWWQQXIZIP-UHFFFAOYSA-N silicon carbide Chemical compound [Si+]#[C-] HBMJWWWQQXIZIP-UHFFFAOYSA-N 0.000 description 1
- 229910010271 silicon carbide Inorganic materials 0.000 description 1
- 239000000377 silicon dioxide Substances 0.000 description 1
- 229920002050 silicone resin Polymers 0.000 description 1
- WBHQBSYUUJJSRZ-UHFFFAOYSA-M sodium bisulfate Chemical compound [Na+].OS([O-])(=O)=O WBHQBSYUUJJSRZ-UHFFFAOYSA-M 0.000 description 1
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- 239000003381 stabilizer Substances 0.000 description 1
- 239000000725 suspension Substances 0.000 description 1
- 238000010558 suspension polymerization method Methods 0.000 description 1
- 239000000454 talc Substances 0.000 description 1
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- 229920001897 terpolymer Polymers 0.000 description 1
- BFKJFAAPBSQJPD-UHFFFAOYSA-N tetrafluoroethene Chemical group FC(F)=C(F)F BFKJFAAPBSQJPD-UHFFFAOYSA-N 0.000 description 1
- 229920001169 thermoplastic Polymers 0.000 description 1
- 239000004416 thermosoftening plastic Substances 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08L—COMPOSITIONS OF MACROMOLECULAR COMPOUNDS
- C08L25/00—Compositions of, homopolymers or copolymers of compounds having one or more unsaturated aliphatic radicals, each having only one carbon-to-carbon double bond, and at least one being terminated by an aromatic carbocyclic ring; Compositions of derivatives of such polymers
- C08L25/02—Homopolymers or copolymers of hydrocarbons
- C08L25/04—Homopolymers or copolymers of styrene
- C08L25/08—Copolymers of styrene
- C08L25/12—Copolymers of styrene with unsaturated nitriles
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08L—COMPOSITIONS OF MACROMOLECULAR COMPOUNDS
- C08L25/00—Compositions of, homopolymers or copolymers of compounds having one or more unsaturated aliphatic radicals, each having only one carbon-to-carbon double bond, and at least one being terminated by an aromatic carbocyclic ring; Compositions of derivatives of such polymers
- C08L25/02—Homopolymers or copolymers of hydrocarbons
- C08L25/16—Homopolymers or copolymers of alkyl-substituted styrenes
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08L—COMPOSITIONS OF MACROMOLECULAR COMPOUNDS
- C08L33/00—Compositions 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; Compositions of derivatives of such polymers
- C08L33/18—Homopolymers or copolymers of nitriles
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08L—COMPOSITIONS OF MACROMOLECULAR COMPOUNDS
- C08L35/00—Compositions of homopolymers or copolymers of compounds having one or more unsaturated aliphatic radicals, each having only one carbon-to-carbon double bond, and at least one being terminated by a carboxyl radical, and containing at least one other carboxyl radical in the molecule, or of salts, anhydrides, esters, amides, imides or nitriles thereof; Compositions of derivatives of such polymers
- C08L35/06—Copolymers with vinyl aromatic monomers
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08L—COMPOSITIONS OF MACROMOLECULAR COMPOUNDS
- C08L25/00—Compositions of, homopolymers or copolymers of compounds having one or more unsaturated aliphatic radicals, each having only one carbon-to-carbon double bond, and at least one being terminated by an aromatic carbocyclic ring; Compositions of derivatives of such polymers
- C08L25/02—Homopolymers or copolymers of hydrocarbons
Landscapes
- Chemical & Material Sciences (AREA)
- Health & Medical Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Medicinal Chemistry (AREA)
- Polymers & Plastics (AREA)
- Organic Chemistry (AREA)
- Addition Polymer Or Copolymer, Post-Treatments, Or Chemical Modifications (AREA)
- Compositions Of Macromolecular Compounds (AREA)
Abstract
Description
Claims (8)
- 말레이미드 단량체(A), 방향족 비닐 단량체(B). 불포화 니트릴 단량체(C) 및 이와 공중합성인 임의의 1종 이상의 기타 공단량체(D)를 탄성 공중합체의 존재 또는 부재하에 공중합시켜서 수득되며, 탄성 중합체를 제외한 단량체 (A), (B), (C) 및 (D)의 조성은 하기 식 (1), (2), (3) 및 (4)를 만족시키며, 고유 점도가 0.3~1.2dl/g인 공중합체 (1) 5~95중량%, 그리고 방향족 비닐 단량체 (B), 불포화 니트릴 (C) 및 이와 공중합성인 임의의 1종 이상의 기타 공단량체(D)를 탄성중합체의 존재 또는 부재하에 공중합시켜서 수득되며, 탄성 중합체를 제외한 단량체 (B), (C) 및 (D)의 조성은 하기식(5) 및 (6)을 만족시키며, 고유점도가 0.3~1.5dl/g인 공중합체(Ⅱ) 95~5중량%로 이루어지며, 공중합체(Ⅰ)중 탄성 중합체를 제외한 단량체 (A), (B), (C) 및 (D)의 전체 중량에 대한 말레이미드 단량체(A)와 불포화 니트릴 단량체(C)의 총 중량%와, 공중합체(Ⅱ)중 탄성 중합체를 제외한 단량체(B), (C) 및 (D)의 전체 중량에 대한 불포화 니트릴 단량체(C)의 중량%는 하기식 :[말레이미드 단량체(A)와 불포화 니트릴 단량체(C)의 총 중량%] - [불포화 니트릴 단량체(C)의 중량%]=+40~-15중량%를 만족시키며, 공중합체(Ⅰ)과 (Ⅱ)의 고유 점도는 하기식 :[공중합체(Ⅰ)의 고유점도] - [공중합체(Ⅱ)의 고유점도]= +0.5~-1.2dl/g을 만족시킴을 특징으로 하는 내열성 공중합체 조성물.
- 제1항에 있어서, 공중합체(Ⅰ) 5~90중량%, 공중합체(Ⅱ) 5~90중량%, 그리고 또한 열가소성 수지 및 탄성 중합체로 구성된 군으로부터 선택되는 1종 이상의 기타 중합체 성분 0.5~90중량%로 이루어짐을 특징으로 하는 내열성 공중합체 조성물.
- 제1항에 있어서, 공중합체(Ⅰ)중 탄성 중합체를 제외한 단량체(A), (B), (C) 및 (D)의 전체 중량에 대한 말레이미드 단량체(A)와 불포화 니트릴 단량체(C)의 총 중량%와, 공중합체(Ⅱ)중 탄성 중합체를 제외한 단량체(B), (C) 및 (D)의 전체 중량에 대한 불포화 니트릴 단량체(C)의 중량%는 하기 식 :[말레이미드 단량체(A)와 불포화 니트릴 단량체(C)의 총 중량%]-[불포화 니트릴 단량체(C)의 중량%]=+30~-10 중량%를 만족시키며, 공중합체(Ⅰ)과 (Ⅱ)의 점도는 하기 식 :[공중합체(Ⅰ)의 고유점도]-[공중합체(Ⅱ)의 고유점도]=+0.4~-0.8dl/g을 만족시킴을 특징으로 하는 내열성 공중합체 조성물.
- 제2항에 있어서, 공중합체(Ⅰ) 중 탄성 중합체를 제외한 단량체 (A), (B), (C) 및 (D)의 전체 중량에 대한 말레아미드 단량체(A)와 불포화 니트릴 단량체(C)의 총 중량%와, 공중합체(Ⅱ)중 탄성 중합체를 제외한 단량체(B), (C) 및 (D)의 전체 중량에 대한 불포화 니트릴 단량체(C)의 중량%는 하기식:[말레이미드 단량체(A)와 불포화 니트릴 단량체(C)의 총 중량%]-[불포화 니트릴 단량체(C)의 중량%]= +35~-10중량%를 만족시키며, 공중합체(Ⅰ)과 (Ⅱ)의 점도는 하기식 :[공중합체(Ⅰ)의 고유점도]-[공중합체(Ⅱ)의 고유점도]=+0.4~-0.8dl/g을 만족시킴을 특징으로 하는 내열성 공중합체 조성물.
Applications Claiming Priority (3)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP270521/1986 | 1986-11-12 | ||
JP61270521A JPS63122746A (ja) | 1986-11-12 | 1986-11-12 | 耐熱性共重合体組成物 |
JP61-270521 | 1986-11-12 |
Publications (2)
Publication Number | Publication Date |
---|---|
KR880006315A KR880006315A (ko) | 1988-07-22 |
KR960002983B1 true KR960002983B1 (ko) | 1996-03-02 |
Family
ID=17487382
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
KR1019870012752A KR960002983B1 (ko) | 1986-11-12 | 1987-11-12 | 내열성 공중합체 조성물 |
Country Status (8)
Country | Link |
---|---|
US (1) | US4877833A (ko) |
EP (1) | EP0267574B1 (ko) |
JP (1) | JPS63122746A (ko) |
KR (1) | KR960002983B1 (ko) |
AU (1) | AU597746B2 (ko) |
CA (1) | CA1318424C (ko) |
DE (1) | DE3787251T2 (ko) |
ES (1) | ES2059346T3 (ko) |
Cited By (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
WO2019022544A1 (ko) * | 2017-07-28 | 2019-01-31 | 주식회사 엘지화학 | 공중합체 및 이의 제조방법 |
US11180590B2 (en) | 2017-07-28 | 2021-11-23 | Lg Chem, Ltd. | Copolymer and preparation method therefor |
Families Citing this family (16)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US5418289A (en) * | 1988-10-31 | 1995-05-23 | Ube Cycon Ltd. | Process for producing a thermoplastic resin composition and a graft copolymer |
AU613802B2 (en) * | 1988-10-31 | 1991-08-08 | Mitsubishi Rayon Company Limited | Heat resistant and impact resistant resin composition |
US5091470A (en) * | 1989-04-26 | 1992-02-25 | The Dow Chemical Company | Molding resin |
JP2667550B2 (ja) * | 1989-05-30 | 1997-10-27 | 旭化成工業株式会社 | 熱可塑性共重合体の製造方法 |
JPH0715038B2 (ja) * | 1989-07-26 | 1995-02-22 | 住友ダウ株式会社 | 熱可塑性樹脂組成物 |
CA2065321C (en) * | 1990-06-25 | 2002-02-19 | Mikio Kodama | Thermoplastic resin composition |
GB2289684B (en) * | 1991-10-31 | 1996-06-12 | Tosoh Corp | Maleimide copolymer resin compositions |
US5424380A (en) * | 1991-10-31 | 1995-06-13 | Tosoh Corporation | Resin composition |
US5539030A (en) * | 1992-03-10 | 1996-07-23 | The Dow Chemical Company | Polycarbonate compositions modified with poly(phenylene ether) |
US5262476A (en) * | 1992-03-10 | 1993-11-16 | The Dow Chemical Company | Polycarbonate/polyester blends modified with poly(phenylene ether) |
CA2110285C (en) * | 1992-03-31 | 2002-11-12 | Yasutoshi Jagawa | Glass fiber-reinforced thermoplastic resin composition |
EP0628578A3 (de) * | 1993-06-11 | 1995-09-27 | Chemie Linz Gmbh | 2,6-Dimethylphenylphenymaleinimid als Comonomeres für Styrolcopolymerisate und Vinylchloridcopolymerisate. |
KR20090076753A (ko) * | 2008-01-08 | 2009-07-13 | 주식회사 엘지화학 | 투명한 수지 조성물 |
KR20090076754A (ko) * | 2008-01-08 | 2009-07-13 | 주식회사 엘지화학 | 광학 필름, 위상차 필름, 보호 필름 및 이들을 포함하는액정 표시 장치 |
KR101105424B1 (ko) * | 2008-04-30 | 2012-01-17 | 주식회사 엘지화학 | 수지 조성물 및 이를 이용하여 형성된 광학 필름 |
US8613986B2 (en) | 2008-04-30 | 2013-12-24 | Lg Chem, Ltd. | Optical film and information technology apparatus comprising the same |
Family Cites Families (16)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US3766142A (en) * | 1964-04-21 | 1973-10-16 | Ici Ltd | Acrylonitrile copolymers |
US4404322A (en) * | 1981-01-28 | 1983-09-13 | Denki Kagaku Kogyo Kabushiki Kaisha | Heat resistant resin composition |
US4374951A (en) * | 1981-09-11 | 1983-02-22 | Monsanto Company | Polyblends comprising N-phenylmaleimide copolymers and SAN copolymers |
JPS58206657A (ja) * | 1982-05-26 | 1983-12-01 | Denki Kagaku Kogyo Kk | 熱可塑性樹脂組成物 |
JPS59135245A (ja) * | 1983-01-25 | 1984-08-03 | Denki Kagaku Kogyo Kk | 熱可塑性樹脂組成物 |
JPS59232138A (ja) * | 1983-06-15 | 1984-12-26 | Mitsubishi Monsanto Chem Co | 耐熱性耐衝撃性樹脂組成物 |
US4585832A (en) * | 1983-06-23 | 1986-04-29 | Mitsubishi Monsanto Chemical Company | Weather and impact resistant resin composition and process for its preparation |
JPH068374B2 (ja) * | 1983-07-19 | 1994-02-02 | 電気化学工業株式会社 | 熱可塑性樹脂組成物 |
JPS6031552A (ja) * | 1983-07-29 | 1985-02-18 | Toray Ind Inc | 熱可塑性樹脂組成物 |
US4663390A (en) * | 1983-10-03 | 1987-05-05 | Atlantic Richfield Company | Methylmethacrylate/phenylmaleimide copolymer and styrene/maleic anhydride copolymer containing polymer alloys |
US4559386A (en) * | 1983-11-21 | 1985-12-17 | Monsanto Company | ABS compositions and process for preparing same |
JPS6173755A (ja) * | 1984-09-18 | 1986-04-15 | Sumitomo Naugatuck Co Ltd | 熱可塑性樹脂組成物 |
JPS59187046A (ja) * | 1984-10-05 | 1984-10-24 | Mitsubishi Monsanto Chem Co | ガラス繊維強化耐熱性樹脂組成物 |
JPS61101547A (ja) * | 1984-10-25 | 1986-05-20 | Sumitomo Naugatuck Co Ltd | 樹脂組成物 |
JPS62207346A (ja) * | 1986-03-07 | 1987-09-11 | Denki Kagaku Kogyo Kk | 透明樹脂組成物 |
US4701493A (en) * | 1986-07-14 | 1987-10-20 | Atlantic Richfield Company | Acrylic modified N-arylmaleimide copolymer molding composition |
-
1986
- 1986-11-12 JP JP61270521A patent/JPS63122746A/ja active Pending
-
1987
- 1987-11-06 US US07/117,561 patent/US4877833A/en not_active Expired - Fee Related
- 1987-11-10 EP EP87116567A patent/EP0267574B1/en not_active Expired - Lifetime
- 1987-11-10 ES ES87116567T patent/ES2059346T3/es not_active Expired - Lifetime
- 1987-11-10 CA CA000551503A patent/CA1318424C/en not_active Expired - Fee Related
- 1987-11-10 DE DE87116567T patent/DE3787251T2/de not_active Expired - Fee Related
- 1987-11-11 AU AU80993/87A patent/AU597746B2/en not_active Ceased
- 1987-11-12 KR KR1019870012752A patent/KR960002983B1/ko not_active IP Right Cessation
Cited By (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
WO2019022544A1 (ko) * | 2017-07-28 | 2019-01-31 | 주식회사 엘지화학 | 공중합체 및 이의 제조방법 |
US11180590B2 (en) | 2017-07-28 | 2021-11-23 | Lg Chem, Ltd. | Copolymer and preparation method therefor |
Also Published As
Publication number | Publication date |
---|---|
KR880006315A (ko) | 1988-07-22 |
ES2059346T3 (es) | 1994-11-16 |
US4877833A (en) | 1989-10-31 |
EP0267574A2 (en) | 1988-05-18 |
AU8099387A (en) | 1988-05-19 |
CA1318424C (en) | 1993-05-25 |
DE3787251T2 (de) | 1994-03-17 |
DE3787251D1 (de) | 1993-10-07 |
AU597746B2 (en) | 1990-06-07 |
EP0267574B1 (en) | 1993-09-01 |
EP0267574A3 (en) | 1990-01-31 |
JPS63122746A (ja) | 1988-05-26 |
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