KR101404907B1 - 낮은 광택도 및 저온 충격 성능을 갖는 열가소성 조성물 - Google Patents
낮은 광택도 및 저온 충격 성능을 갖는 열가소성 조성물 Download PDFInfo
- Publication number
- KR101404907B1 KR101404907B1 KR1020097009001A KR20097009001A KR101404907B1 KR 101404907 B1 KR101404907 B1 KR 101404907B1 KR 1020097009001 A KR1020097009001 A KR 1020097009001A KR 20097009001 A KR20097009001 A KR 20097009001A KR 101404907 B1 KR101404907 B1 KR 101404907B1
- Authority
- KR
- South Korea
- Prior art keywords
- composition
- acrylate
- glycidyl
- meth
- polymer
- 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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- 239000000203 mixture Substances 0.000 title claims abstract description 67
- 229920001169 thermoplastic Polymers 0.000 title abstract description 13
- 239000004416 thermosoftening plastic Substances 0.000 title abstract description 13
- -1 glycidyl ester Chemical class 0.000 claims abstract description 56
- 239000000178 monomer Substances 0.000 claims abstract description 37
- 125000003118 aryl group Chemical group 0.000 claims abstract description 31
- 229920001971 elastomer Polymers 0.000 claims abstract description 30
- 239000005060 rubber Substances 0.000 claims abstract description 30
- NIXOWILDQLNWCW-UHFFFAOYSA-M Acrylate Chemical compound [O-]C(=O)C=C NIXOWILDQLNWCW-UHFFFAOYSA-M 0.000 claims abstract description 24
- 229920000578 graft copolymer Polymers 0.000 claims abstract description 21
- 229920001296 polysiloxane Polymers 0.000 claims abstract description 14
- BVKZGUZCCUSVTD-UHFFFAOYSA-L Carbonate Chemical compound [O-]C([O-])=O BVKZGUZCCUSVTD-UHFFFAOYSA-L 0.000 claims abstract description 13
- 150000002148 esters Chemical class 0.000 claims abstract description 11
- 125000005250 alkyl acrylate group Chemical group 0.000 claims abstract description 10
- 229920001002 functional polymer Polymers 0.000 claims abstract description 10
- DQXBYHZEEUGOBF-UHFFFAOYSA-N but-3-enoic acid;ethene Chemical compound C=C.OC(=O)CC=C DQXBYHZEEUGOBF-UHFFFAOYSA-N 0.000 claims abstract description 5
- 239000005038 ethylene vinyl acetate Substances 0.000 claims abstract description 5
- 229920001084 poly(chloroprene) Polymers 0.000 claims abstract description 5
- 229920001200 poly(ethylene-vinyl acetate) Polymers 0.000 claims abstract description 5
- 229920002635 polyurethane Polymers 0.000 claims abstract description 5
- 239000004814 polyurethane Substances 0.000 claims abstract description 5
- 229920001577 copolymer Polymers 0.000 claims description 19
- 229920000642 polymer Polymers 0.000 claims description 15
- VGGSQFUCUMXWEO-UHFFFAOYSA-N Ethene Chemical compound C=C VGGSQFUCUMXWEO-UHFFFAOYSA-N 0.000 claims description 13
- 239000005977 Ethylene Substances 0.000 claims description 13
- 229920000122 acrylonitrile butadiene styrene Polymers 0.000 claims description 10
- VVQNEPGJFQJSBK-UHFFFAOYSA-N Methyl methacrylate Chemical compound COC(=O)C(C)=C VVQNEPGJFQJSBK-UHFFFAOYSA-N 0.000 claims description 9
- XECAHXYUAAWDEL-UHFFFAOYSA-N acrylonitrile butadiene styrene Chemical group C=CC=C.C=CC#N.C=CC1=CC=CC=C1 XECAHXYUAAWDEL-UHFFFAOYSA-N 0.000 claims description 9
- 239000004676 acrylonitrile butadiene styrene Substances 0.000 claims description 9
- IISBACLAFKSPIT-UHFFFAOYSA-N bisphenol A Chemical compound C=1C=C(O)C=CC=1C(C)(C)C1=CC=C(O)C=C1 IISBACLAFKSPIT-UHFFFAOYSA-N 0.000 claims description 9
- VOZRXNHHFUQHIL-UHFFFAOYSA-N glycidyl methacrylate Chemical compound CC(=C)C(=O)OCC1CO1 VOZRXNHHFUQHIL-UHFFFAOYSA-N 0.000 claims description 9
- 238000000034 method Methods 0.000 claims description 8
- 239000002245 particle Substances 0.000 claims description 8
- 229920002554 vinyl polymer Polymers 0.000 claims description 8
- RPQRDASANLAFCM-UHFFFAOYSA-N oxiran-2-ylmethyl prop-2-enoate Chemical group C=CC(=O)OCC1CO1 RPQRDASANLAFCM-UHFFFAOYSA-N 0.000 claims description 7
- 229920000058 polyacrylate Polymers 0.000 claims description 6
- 125000003055 glycidyl group Chemical group C(C1CO1)* 0.000 claims description 5
- 229920005989 resin Polymers 0.000 claims description 5
- 239000011347 resin Substances 0.000 claims description 5
- 150000001252 acrylic acid derivatives Chemical class 0.000 claims description 4
- 239000003795 chemical substances by application Substances 0.000 claims description 4
- YWAKXRMUMFPDSH-UHFFFAOYSA-N pentene Chemical compound CCCC=C YWAKXRMUMFPDSH-UHFFFAOYSA-N 0.000 claims description 4
- 229920002857 polybutadiene Polymers 0.000 claims description 4
- 239000005062 Polybutadiene Substances 0.000 claims description 3
- 239000012760 heat stabilizer Substances 0.000 claims description 3
- 238000010557 suspension polymerization reaction Methods 0.000 claims description 3
- 125000000391 vinyl group Chemical group [H]C([*])=C([H])[H] 0.000 claims description 3
- 239000002216 antistatic agent Substances 0.000 claims description 2
- 239000000945 filler Substances 0.000 claims description 2
- 229920001519 homopolymer Polymers 0.000 claims description 2
- 230000003301 hydrolyzing effect Effects 0.000 claims description 2
- 239000004611 light stabiliser Substances 0.000 claims description 2
- 239000000314 lubricant Substances 0.000 claims description 2
- 239000002667 nucleating agent Substances 0.000 claims description 2
- 239000012744 reinforcing agent Substances 0.000 claims description 2
- 239000003381 stabilizer Substances 0.000 claims description 2
- 229920001567 vinyl ester resin Polymers 0.000 claims description 2
- LLVWLCAZSOLOTF-UHFFFAOYSA-N 1-methyl-4-[1,4,4-tris(4-methylphenyl)buta-1,3-dienyl]benzene Chemical compound C1=CC(C)=CC=C1C(C=1C=CC(C)=CC=1)=CC=C(C=1C=CC(C)=CC=1)C1=CC=C(C)C=C1 LLVWLCAZSOLOTF-UHFFFAOYSA-N 0.000 claims 2
- 239000003086 colorant Substances 0.000 claims 1
- 150000001993 dienes Chemical class 0.000 claims 1
- HQQADJVZYDDRJT-UHFFFAOYSA-N ethene;prop-1-ene Chemical group C=C.CC=C HQQADJVZYDDRJT-UHFFFAOYSA-N 0.000 claims 1
- 239000000049 pigment Substances 0.000 claims 1
- 229920001485 poly(butyl acrylate) polymer Polymers 0.000 claims 1
- 229920006027 ternary co-polymer Polymers 0.000 claims 1
- 230000007704 transition Effects 0.000 claims 1
- 229920000515 polycarbonate Polymers 0.000 abstract description 15
- 239000004417 polycarbonate Substances 0.000 abstract description 14
- 229920003244 diene elastomer Polymers 0.000 abstract description 6
- 229920002943 EPDM rubber Polymers 0.000 abstract description 4
- 229920000193 polymethacrylate Polymers 0.000 abstract description 3
- 239000000758 substrate Substances 0.000 abstract description 2
- 150000001875 compounds Chemical class 0.000 description 19
- PPBRXRYQALVLMV-UHFFFAOYSA-N Styrene Chemical compound C=CC1=CC=CC=C1 PPBRXRYQALVLMV-UHFFFAOYSA-N 0.000 description 12
- 125000000217 alkyl group Chemical group 0.000 description 8
- 150000004649 carbonic acid derivatives Chemical class 0.000 description 7
- BAPJBEWLBFYGME-UHFFFAOYSA-N Methyl acrylate Chemical group COC(=O)C=C BAPJBEWLBFYGME-UHFFFAOYSA-N 0.000 description 6
- 229920000728 polyester Polymers 0.000 description 6
- 125000004203 4-hydroxyphenyl group Chemical group [H]OC1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 description 5
- ISWSIDIOOBJBQZ-UHFFFAOYSA-N Phenol Chemical compound OC1=CC=CC=C1 ISWSIDIOOBJBQZ-UHFFFAOYSA-N 0.000 description 5
- XUIMIQQOPSSXEZ-UHFFFAOYSA-N Silicon Chemical group [Si] XUIMIQQOPSSXEZ-UHFFFAOYSA-N 0.000 description 5
- CQEYYJKEWSMYFG-UHFFFAOYSA-N butyl acrylate Chemical compound CCCCOC(=O)C=C CQEYYJKEWSMYFG-UHFFFAOYSA-N 0.000 description 5
- 239000003431 cross linking reagent Substances 0.000 description 5
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 description 5
- 229920001897 terpolymer Polymers 0.000 description 5
- NLHHRLWOUZZQLW-UHFFFAOYSA-N Acrylonitrile Chemical compound C=CC#N NLHHRLWOUZZQLW-UHFFFAOYSA-N 0.000 description 4
- JIGUQPWFLRLWPJ-UHFFFAOYSA-N Ethyl acrylate Chemical compound CCOC(=O)C=C JIGUQPWFLRLWPJ-UHFFFAOYSA-N 0.000 description 4
- KKEYFWRCBNTPAC-UHFFFAOYSA-N Terephthalic acid Chemical compound OC(=O)C1=CC=C(C(O)=O)C=C1 KKEYFWRCBNTPAC-UHFFFAOYSA-N 0.000 description 4
- 239000002131 composite material Substances 0.000 description 4
- QQVIHTHCMHWDBS-UHFFFAOYSA-N isophthalic acid Chemical compound OC(=O)C1=CC=CC(C(O)=O)=C1 QQVIHTHCMHWDBS-UHFFFAOYSA-N 0.000 description 4
- 125000005375 organosiloxane group Chemical group 0.000 description 4
- PNJWIWWMYCMZRO-UHFFFAOYSA-N pent‐4‐en‐2‐one Natural products CC(=O)CC=C PNJWIWWMYCMZRO-UHFFFAOYSA-N 0.000 description 4
- 238000002360 preparation method Methods 0.000 description 4
- 229910052710 silicon Inorganic materials 0.000 description 4
- 239000010703 silicon Substances 0.000 description 4
- 229920000181 Ethylene propylene rubber Polymers 0.000 description 3
- 239000006085 branching agent Substances 0.000 description 3
- 125000004432 carbon atom Chemical group C* 0.000 description 3
- 125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 description 3
- 238000010559 graft polymerization reaction Methods 0.000 description 3
- 229910052739 hydrogen Inorganic materials 0.000 description 3
- 239000001257 hydrogen Substances 0.000 description 3
- 239000000463 material Substances 0.000 description 3
- FBCQUCJYYPMKRO-UHFFFAOYSA-N prop-2-enyl 2-methylprop-2-enoate Chemical compound CC(=C)C(=O)OCC=C FBCQUCJYYPMKRO-UHFFFAOYSA-N 0.000 description 3
- 150000003254 radicals Chemical group 0.000 description 3
- MYRTYDVEIRVNKP-UHFFFAOYSA-N 1,2-Divinylbenzene Chemical compound C=CC1=CC=CC=C1C=C MYRTYDVEIRVNKP-UHFFFAOYSA-N 0.000 description 2
- KPZGRMZPZLOPBS-UHFFFAOYSA-N 1,3-dichloro-2,2-bis(chloromethyl)propane Chemical compound ClCC(CCl)(CCl)CCl KPZGRMZPZLOPBS-UHFFFAOYSA-N 0.000 description 2
- SMZOUWXMTYCWNB-UHFFFAOYSA-N 2-(2-methoxy-5-methylphenyl)ethanamine Chemical compound COC1=CC=C(C)C=C1CCN SMZOUWXMTYCWNB-UHFFFAOYSA-N 0.000 description 2
- JAHNSTQSQJOJLO-UHFFFAOYSA-N 2-(3-fluorophenyl)-1h-imidazole Chemical compound FC1=CC=CC(C=2NC=CN=2)=C1 JAHNSTQSQJOJLO-UHFFFAOYSA-N 0.000 description 2
- NIXOWILDQLNWCW-UHFFFAOYSA-N 2-Propenoic acid Natural products OC(=O)C=C NIXOWILDQLNWCW-UHFFFAOYSA-N 0.000 description 2
- DBCAQXHNJOFNGC-UHFFFAOYSA-N 4-bromo-1,1,1-trifluorobutane Chemical compound FC(F)(F)CCCBr DBCAQXHNJOFNGC-UHFFFAOYSA-N 0.000 description 2
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 description 2
- QIGBRXMKCJKVMJ-UHFFFAOYSA-N Hydroquinone Chemical compound OC1=CC=C(O)C=C1 QIGBRXMKCJKVMJ-UHFFFAOYSA-N 0.000 description 2
- 239000004609 Impact Modifier Substances 0.000 description 2
- CERQOIWHTDAKMF-UHFFFAOYSA-N Methacrylic acid Chemical compound CC(=C)C(O)=O CERQOIWHTDAKMF-UHFFFAOYSA-N 0.000 description 2
- GYCMBHHDWRMZGG-UHFFFAOYSA-N Methylacrylonitrile Chemical compound CC(=C)C#N GYCMBHHDWRMZGG-UHFFFAOYSA-N 0.000 description 2
- 229920000297 Rayon Polymers 0.000 description 2
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 description 2
- YXFVVABEGXRONW-UHFFFAOYSA-N Toluene Natural products CC1=CC=CC=C1 YXFVVABEGXRONW-UHFFFAOYSA-N 0.000 description 2
- 150000008064 anhydrides Chemical class 0.000 description 2
- 229910052799 carbon Inorganic materials 0.000 description 2
- 150000001735 carboxylic acids Chemical class 0.000 description 2
- USIUVYZYUHIAEV-UHFFFAOYSA-N diphenyl ether Chemical compound C=1C=CC=CC=1OC1=CC=CC=C1 USIUVYZYUHIAEV-UHFFFAOYSA-N 0.000 description 2
- KPUWHANPEXNPJT-UHFFFAOYSA-N disiloxane Chemical class [SiH3]O[SiH3] KPUWHANPEXNPJT-UHFFFAOYSA-N 0.000 description 2
- 239000000839 emulsion Substances 0.000 description 2
- STVZJERGLQHEKB-UHFFFAOYSA-N ethylene glycol dimethacrylate Substances CC(=C)C(=O)OCCOC(=O)C(C)=C STVZJERGLQHEKB-UHFFFAOYSA-N 0.000 description 2
- 230000009477 glass transition Effects 0.000 description 2
- 125000004464 hydroxyphenyl group Chemical group 0.000 description 2
- FPYJFEHAWHCUMM-UHFFFAOYSA-N maleic anhydride Chemical compound O=C1OC(=O)C=C1 FPYJFEHAWHCUMM-UHFFFAOYSA-N 0.000 description 2
- 239000000155 melt Substances 0.000 description 2
- LVHBHZANLOWSRM-UHFFFAOYSA-N methylenebutanedioic acid Natural products OC(=O)CC(=C)C(O)=O LVHBHZANLOWSRM-UHFFFAOYSA-N 0.000 description 2
- 238000000465 moulding Methods 0.000 description 2
- CYIDZMCFTVVTJO-UHFFFAOYSA-N pyromellitic acid Chemical compound OC(=O)C1=CC(C(O)=O)=C(C(O)=O)C=C1C(O)=O CYIDZMCFTVVTJO-UHFFFAOYSA-N 0.000 description 2
- GHMLBKRAJCXXBS-UHFFFAOYSA-N resorcinol Chemical compound OC1=CC=CC(O)=C1 GHMLBKRAJCXXBS-UHFFFAOYSA-N 0.000 description 2
- GRJISGHXMUQUMC-UHFFFAOYSA-N silyl prop-2-enoate Chemical compound [SiH3]OC(=O)C=C GRJISGHXMUQUMC-UHFFFAOYSA-N 0.000 description 2
- 238000012360 testing method Methods 0.000 description 2
- PXDIIXCXCVILQI-UHFFFAOYSA-N (4-ethenylphenyl)-dimethoxy-methylsilane Chemical compound CO[Si](C)(OC)C1=CC=C(C=C)C=C1 PXDIIXCXCVILQI-UHFFFAOYSA-N 0.000 description 1
- 125000004209 (C1-C8) alkyl group Chemical group 0.000 description 1
- KOMNUTZXSVSERR-UHFFFAOYSA-N 1,3,5-tris(prop-2-enyl)-1,3,5-triazinane-2,4,6-trione Chemical compound C=CCN1C(=O)N(CC=C)C(=O)N(CC=C)C1=O KOMNUTZXSVSERR-UHFFFAOYSA-N 0.000 description 1
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- VJDVKNLYGQTELS-UHFFFAOYSA-N 1,3-dichloro-2-ethenyl-5-methylbenzene Chemical compound CC1=CC(Cl)=C(C=C)C(Cl)=C1 VJDVKNLYGQTELS-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
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- 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
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- VSIKJPJINIDELZ-UHFFFAOYSA-N 2,2,4,4,6,6,8,8-octakis-phenyl-1,3,5,7,2,4,6,8-tetraoxatetrasilocane Chemical compound O1[Si](C=2C=CC=CC=2)(C=2C=CC=CC=2)O[Si](C=2C=CC=CC=2)(C=2C=CC=CC=2)O[Si](C=2C=CC=CC=2)(C=2C=CC=CC=2)O[Si]1(C=1C=CC=CC=1)C1=CC=CC=C1 VSIKJPJINIDELZ-UHFFFAOYSA-N 0.000 description 1
- VMAWODUEPLAHOE-UHFFFAOYSA-N 2,4,6,8-tetrakis(ethenyl)-2,4,6,8-tetramethyl-1,3,5,7,2,4,6,8-tetraoxatetrasilocane Chemical class C=C[Si]1(C)O[Si](C)(C=C)O[Si](C)(C=C)O[Si](C)(C=C)O1 VMAWODUEPLAHOE-UHFFFAOYSA-N 0.000 description 1
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- CUAUDSWILJWDOD-UHFFFAOYSA-N 4-(3,5-dimethylheptyl)phenol Chemical compound CCC(C)CC(C)CCC1=CC=C(O)C=C1 CUAUDSWILJWDOD-UHFFFAOYSA-N 0.000 description 1
- HVXRCAWUNAOCTA-UHFFFAOYSA-N 4-(6-methylheptyl)phenol Chemical compound CC(C)CCCCCC1=CC=C(O)C=C1 HVXRCAWUNAOCTA-UHFFFAOYSA-N 0.000 description 1
- UMPGNGRIGSEMTC-UHFFFAOYSA-N 4-[1-(4-hydroxyphenyl)-3,3,5-trimethylcyclohexyl]phenol Chemical compound C1C(C)CC(C)(C)CC1(C=1C=CC(O)=CC=1)C1=CC=C(O)C=C1 UMPGNGRIGSEMTC-UHFFFAOYSA-N 0.000 description 1
- NIRYBKWMEWFDPM-UHFFFAOYSA-N 4-[3-(4-hydroxyphenyl)-3-methylbutyl]phenol Chemical compound C=1C=C(O)C=CC=1C(C)(C)CCC1=CC=C(O)C=C1 NIRYBKWMEWFDPM-UHFFFAOYSA-N 0.000 description 1
- WXNZTHHGJRFXKQ-UHFFFAOYSA-N 4-chlorophenol Chemical compound OC1=CC=C(Cl)C=C1 WXNZTHHGJRFXKQ-UHFFFAOYSA-N 0.000 description 1
- ISAVYTVYFVQUDY-UHFFFAOYSA-N 4-tert-Octylphenol Chemical compound CC(C)(C)CC(C)(C)C1=CC=C(O)C=C1 ISAVYTVYFVQUDY-UHFFFAOYSA-N 0.000 description 1
- QHPQWRBYOIRBIT-UHFFFAOYSA-N 4-tert-butylphenol Chemical compound CC(C)(C)C1=CC=C(O)C=C1 QHPQWRBYOIRBIT-UHFFFAOYSA-N 0.000 description 1
- RFZCFUBJKXZILU-UHFFFAOYSA-N 5,6-diphenylbenzene-1,2,4-triol Chemical compound OC=1C(=C(C(=C(C1)O)C1=CC=CC=C1)C1=CC=CC=C1)O RFZCFUBJKXZILU-UHFFFAOYSA-N 0.000 description 1
- YAAQEISEHDUIFO-UHFFFAOYSA-N C=CC#N.OC(=O)C=CC=CC1=CC=CC=C1 Chemical compound C=CC#N.OC(=O)C=CC=CC1=CC=CC=C1 YAAQEISEHDUIFO-UHFFFAOYSA-N 0.000 description 1
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- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 description 1
- 239000004971 Cross linker Substances 0.000 description 1
- XMSXQFUHVRWGNA-UHFFFAOYSA-N Decamethylcyclopentasiloxane Chemical compound C[Si]1(C)O[Si](C)(C)O[Si](C)(C)O[Si](C)(C)O[Si](C)(C)O1 XMSXQFUHVRWGNA-UHFFFAOYSA-N 0.000 description 1
- IUMSDRXLFWAGNT-UHFFFAOYSA-N Dodecamethylcyclohexasiloxane Chemical compound C[Si]1(C)O[Si](C)(C)O[Si](C)(C)O[Si](C)(C)O[Si](C)(C)O[Si](C)(C)O1 IUMSDRXLFWAGNT-UHFFFAOYSA-N 0.000 description 1
- MHAJPDPJQMAIIY-UHFFFAOYSA-N Hydrogen peroxide Chemical compound OO MHAJPDPJQMAIIY-UHFFFAOYSA-N 0.000 description 1
- 238000012696 Interfacial polycondensation Methods 0.000 description 1
- 239000004425 Makrolon Substances 0.000 description 1
- OFOBLEOULBTSOW-UHFFFAOYSA-N Malonic acid Chemical compound OC(=O)CC(O)=O OFOBLEOULBTSOW-UHFFFAOYSA-N 0.000 description 1
- CERQOIWHTDAKMF-UHFFFAOYSA-M Methacrylate Chemical compound CC(=C)C([O-])=O CERQOIWHTDAKMF-UHFFFAOYSA-M 0.000 description 1
- 208000002991 Ring chromosome 4 syndrome Diseases 0.000 description 1
- BOTDANWDWHJENH-UHFFFAOYSA-N Tetraethyl orthosilicate Chemical compound CCO[Si](OCC)(OCC)OCC BOTDANWDWHJENH-UHFFFAOYSA-N 0.000 description 1
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- OCKWAZCWKSMKNC-UHFFFAOYSA-N [3-octadecanoyloxy-2,2-bis(octadecanoyloxymethyl)propyl] octadecanoate Chemical compound CCCCCCCCCCCCCCCCCC(=O)OCC(COC(=O)CCCCCCCCCCCCCCCCC)(COC(=O)CCCCCCCCCCCCCCCCC)COC(=O)CCCCCCCCCCCCCCCCC OCKWAZCWKSMKNC-UHFFFAOYSA-N 0.000 description 1
- 230000002378 acidificating effect Effects 0.000 description 1
- 229920002877 acrylic styrene acrylonitrile Polymers 0.000 description 1
- 239000000654 additive Substances 0.000 description 1
- 230000002411 adverse 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
- 125000004103 aminoalkyl group Chemical group 0.000 description 1
- 239000012874 anionic emulsifier Substances 0.000 description 1
- 125000004429 atom Chemical group 0.000 description 1
- UHOVQNZJYSORNB-UHFFFAOYSA-N benzene Substances C1=CC=CC=C1 UHOVQNZJYSORNB-UHFFFAOYSA-N 0.000 description 1
- UWCPYKQBIPYOLX-UHFFFAOYSA-N benzene-1,3,5-tricarbonyl chloride Chemical compound ClC(=O)C1=CC(C(Cl)=O)=CC(C(Cl)=O)=C1 UWCPYKQBIPYOLX-UHFFFAOYSA-N 0.000 description 1
- VCCBEIPGXKNHFW-UHFFFAOYSA-N biphenyl-4,4'-diol Chemical group C1=CC(O)=CC=C1C1=CC=C(O)C=C1 VCCBEIPGXKNHFW-UHFFFAOYSA-N 0.000 description 1
- ZPOLOEWJWXZUSP-AATRIKPKSA-N bis(prop-2-enyl) (e)-but-2-enedioate Chemical compound C=CCOC(=O)\C=C\C(=O)OCC=C ZPOLOEWJWXZUSP-AATRIKPKSA-N 0.000 description 1
- ZPOLOEWJWXZUSP-WAYWQWQTSA-N bis(prop-2-enyl) (z)-but-2-enedioate Chemical compound C=CCOC(=O)\C=C/C(=O)OCC=C ZPOLOEWJWXZUSP-WAYWQWQTSA-N 0.000 description 1
- FPODCVUTIPDRTE-UHFFFAOYSA-N bis(prop-2-enyl) hexanedioate Chemical compound C=CCOC(=O)CCCCC(=O)OCC=C FPODCVUTIPDRTE-UHFFFAOYSA-N 0.000 description 1
- 238000000071 blow moulding Methods 0.000 description 1
- SQHOHKQMTHROSF-UHFFFAOYSA-N but-1-en-2-ylbenzene Chemical compound CCC(=C)C1=CC=CC=C1 SQHOHKQMTHROSF-UHFFFAOYSA-N 0.000 description 1
- VUKHQPGJNTXTPY-UHFFFAOYSA-N but-2-enylbenzene Chemical compound CC=CCC1=CC=CC=C1 VUKHQPGJNTXTPY-UHFFFAOYSA-N 0.000 description 1
- 125000005587 carbonate group Chemical group 0.000 description 1
- 238000006243 chemical reaction Methods 0.000 description 1
- HAURRGANAANPSQ-UHFFFAOYSA-N cis-2,4,6-Trimethyl-2,4,6-triphenylcyclotrisiloxane Chemical compound O1[Si](C)(C=2C=CC=CC=2)O[Si](C)(C=2C=CC=CC=2)O[Si]1(C)C1=CC=CC=C1 HAURRGANAANPSQ-UHFFFAOYSA-N 0.000 description 1
- 238000007334 copolymerization reaction Methods 0.000 description 1
- MGNCLNQXLYJVJD-UHFFFAOYSA-N cyanuric chloride Chemical compound ClC1=NC(Cl)=NC(Cl)=N1 MGNCLNQXLYJVJD-UHFFFAOYSA-N 0.000 description 1
- 125000004122 cyclic group Chemical group 0.000 description 1
- OIWOHHBRDFKZNC-UHFFFAOYSA-N cyclohexyl 2-methylprop-2-enoate Chemical compound CC(=C)C(=O)OC1CCCCC1 OIWOHHBRDFKZNC-UHFFFAOYSA-N 0.000 description 1
- 125000000113 cyclohexyl group Chemical group [H]C1([H])C([H])([H])C([H])([H])C([H])(*)C([H])([H])C1([H])[H] 0.000 description 1
- 239000006185 dispersion Substances 0.000 description 1
- GMSCBRSQMRDRCD-UHFFFAOYSA-N dodecyl 2-methylprop-2-enoate Chemical compound CCCCCCCCCCCCOC(=O)C(C)=C GMSCBRSQMRDRCD-UHFFFAOYSA-N 0.000 description 1
- 230000000694 effects Effects 0.000 description 1
- 238000004945 emulsification Methods 0.000 description 1
- 238000010556 emulsion polymerization method Methods 0.000 description 1
- 238000007720 emulsion polymerization reaction Methods 0.000 description 1
- 125000004185 ester group Chemical group 0.000 description 1
- UIWXSTHGICQLQT-UHFFFAOYSA-N ethenyl propanoate Chemical compound CCC(=O)OC=C UIWXSTHGICQLQT-UHFFFAOYSA-N 0.000 description 1
- 230000001747 exhibiting effect Effects 0.000 description 1
- 238000001125 extrusion Methods 0.000 description 1
- 230000002349 favourable effect Effects 0.000 description 1
- 238000005227 gel permeation chromatography Methods 0.000 description 1
- 125000001475 halogen functional group Chemical group 0.000 description 1
- 125000005842 heteroatom Chemical group 0.000 description 1
- HTDJPCNNEPUOOQ-UHFFFAOYSA-N hexamethylcyclotrisiloxane Chemical compound C[Si]1(C)O[Si](C)(C)O[Si](C)(C)O1 HTDJPCNNEPUOOQ-UHFFFAOYSA-N 0.000 description 1
- LNCPIMCVTKXXOY-UHFFFAOYSA-N hexyl 2-methylprop-2-enoate Chemical compound CCCCCCOC(=O)C(C)=C LNCPIMCVTKXXOY-UHFFFAOYSA-N 0.000 description 1
- 125000004435 hydrogen atom Chemical class [H]* 0.000 description 1
- 125000002768 hydroxyalkyl group Chemical group 0.000 description 1
- 150000003949 imides Chemical class 0.000 description 1
- 238000010348 incorporation Methods 0.000 description 1
- 239000003999 initiator Substances 0.000 description 1
- 238000001746 injection moulding Methods 0.000 description 1
- 238000004519 manufacturing process Methods 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
- 238000012986 modification Methods 0.000 description 1
- 230000004048 modification Effects 0.000 description 1
- AKIDPNOWIHDLBQ-UHFFFAOYSA-N naphthalene-1,4,5,8-tetracarbonyl chloride Chemical compound C1=CC(C(Cl)=O)=C2C(C(=O)Cl)=CC=C(C(Cl)=O)C2=C1C(Cl)=O AKIDPNOWIHDLBQ-UHFFFAOYSA-N 0.000 description 1
- RXOHFPCZGPKIRD-UHFFFAOYSA-N naphthalene-2,6-dicarboxylic acid Chemical compound C1=C(C(O)=O)C=CC2=CC(C(=O)O)=CC=C21 RXOHFPCZGPKIRD-UHFFFAOYSA-N 0.000 description 1
- 150000002825 nitriles Chemical class 0.000 description 1
- HMMGMWAXVFQUOA-UHFFFAOYSA-N octamethylcyclotetrasiloxane Chemical compound C[Si]1(C)O[Si](C)(C)O[Si](C)(C)O[Si](C)(C)O1 HMMGMWAXVFQUOA-UHFFFAOYSA-N 0.000 description 1
- 150000004028 organic sulfates Chemical class 0.000 description 1
- 150000002924 oxiranes Chemical class 0.000 description 1
- 150000002978 peroxides Chemical class 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
- 125000005342 perphosphate group Chemical group 0.000 description 1
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 description 1
- 230000000704 physical effect Effects 0.000 description 1
- 238000006068 polycondensation reaction Methods 0.000 description 1
- 229920002959 polymer blend Polymers 0.000 description 1
- QTECDUFMBMSHKR-UHFFFAOYSA-N prop-2-enyl prop-2-enoate Chemical compound C=CCOC(=O)C=C QTECDUFMBMSHKR-UHFFFAOYSA-N 0.000 description 1
- HJWLCRVIBGQPNF-UHFFFAOYSA-N prop-2-enylbenzene Chemical compound C=CCC1=CC=CC=C1 HJWLCRVIBGQPNF-UHFFFAOYSA-N 0.000 description 1
- 239000001294 propane Substances 0.000 description 1
- 125000001436 propyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])[H] 0.000 description 1
- PNXMTCDJUBJHQJ-UHFFFAOYSA-N propyl prop-2-enoate Chemical compound CCCOC(=O)C=C PNXMTCDJUBJHQJ-UHFFFAOYSA-N 0.000 description 1
- 150000003839 salts Chemical class 0.000 description 1
- 150000004756 silanes Chemical class 0.000 description 1
- 239000000377 silicon dioxide Substances 0.000 description 1
- 150000003440 styrenes Chemical class 0.000 description 1
- 125000001424 substituent group Chemical group 0.000 description 1
- 150000008054 sulfonate salts Chemical class 0.000 description 1
- 239000000725 suspension Substances 0.000 description 1
- UQMOLLPKNHFRAC-UHFFFAOYSA-N tetrabutyl silicate Chemical compound CCCCO[Si](OCCCC)(OCCCC)OCCCC UQMOLLPKNHFRAC-UHFFFAOYSA-N 0.000 description 1
- LFQCEHFDDXELDD-UHFFFAOYSA-N tetramethyl orthosilicate Chemical compound CO[Si](OC)(OC)OC LFQCEHFDDXELDD-UHFFFAOYSA-N 0.000 description 1
- ZQZCOBSUOFHDEE-UHFFFAOYSA-N tetrapropyl silicate Chemical compound CCCO[Si](OCCC)(OCCC)OCCC ZQZCOBSUOFHDEE-UHFFFAOYSA-N 0.000 description 1
- 238000009757 thermoplastic moulding Methods 0.000 description 1
- 238000005809 transesterification reaction Methods 0.000 description 1
- 238000004627 transmission electron microscopy Methods 0.000 description 1
- JCVQKRGIASEUKR-UHFFFAOYSA-N triethoxy(phenyl)silane Chemical compound CCO[Si](OCC)(OCC)C1=CC=CC=C1 JCVQKRGIASEUKR-UHFFFAOYSA-N 0.000 description 1
- TUQLLQQWSNWKCF-UHFFFAOYSA-N trimethoxymethylsilane Chemical compound COC([SiH3])(OC)OC TUQLLQQWSNWKCF-UHFFFAOYSA-N 0.000 description 1
- 238000005199 ultracentrifugation Methods 0.000 description 1
- 150000007934 α,β-unsaturated carboxylic acids Chemical class 0.000 description 1
Classifications
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- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08L—COMPOSITIONS OF MACROMOLECULAR COMPOUNDS
- C08L69/00—Compositions of polycarbonates; Compositions of derivatives of polycarbonates
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- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08L—COMPOSITIONS OF MACROMOLECULAR COMPOUNDS
- C08L51/00—Compositions of graft polymers in which the grafted component is obtained by reactions only involving carbon-to-carbon unsaturated bonds; Compositions of derivatives of such polymers
- C08L51/06—Compositions of graft polymers in which the grafted component is obtained by reactions only involving carbon-to-carbon unsaturated bonds; Compositions of derivatives of such polymers grafted on to homopolymers or copolymers of aliphatic hydrocarbons containing only one carbon-to-carbon double bond
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- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08L—COMPOSITIONS OF MACROMOLECULAR COMPOUNDS
- C08L51/00—Compositions of graft polymers in which the grafted component is obtained by reactions only involving carbon-to-carbon unsaturated bonds; Compositions of derivatives of such polymers
- C08L51/08—Compositions of graft polymers in which the grafted component is obtained by reactions only involving carbon-to-carbon unsaturated bonds; Compositions of derivatives of such polymers grafted on to macromolecular compounds obtained otherwise than by reactions only involving unsaturated carbon-to-carbon bonds
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- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08L—COMPOSITIONS OF MACROMOLECULAR COMPOUNDS
- C08L53/00—Compositions of block copolymers containing at least one sequence of a polymer obtained by reactions only involving carbon-to-carbon unsaturated bonds; Compositions of derivatives of such polymers
- C08L53/02—Compositions of block copolymers containing at least one sequence of a polymer obtained by reactions only involving carbon-to-carbon unsaturated bonds; Compositions of derivatives of such polymers of vinyl-aromatic monomers and conjugated dienes
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- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08L—COMPOSITIONS OF MACROMOLECULAR COMPOUNDS
- C08L69/00—Compositions of polycarbonates; Compositions of derivatives of polycarbonates
- C08L69/005—Polyester-carbonates
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- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08L—COMPOSITIONS OF MACROMOLECULAR COMPOUNDS
- C08L23/00—Compositions of homopolymers or copolymers of unsaturated aliphatic hydrocarbons having only one carbon-to-carbon double bond; Compositions of derivatives of such polymers
- C08L23/02—Compositions of homopolymers or copolymers of unsaturated aliphatic hydrocarbons having only one carbon-to-carbon double bond; Compositions of derivatives of such polymers not modified by chemical after-treatment
- C08L23/04—Homopolymers or copolymers of ethene
- C08L23/08—Copolymers of ethene
- C08L23/0846—Copolymers of ethene with unsaturated hydrocarbons containing atoms other than carbon or hydrogen
- C08L23/0869—Copolymers of ethene with unsaturated hydrocarbons containing atoms other than carbon or hydrogen with unsaturated acids, e.g. [meth]acrylic acid; with unsaturated esters, e.g. [meth]acrylic acid esters
- C08L23/0884—Epoxide-containing esters
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- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08L—COMPOSITIONS OF MACROMOLECULAR COMPOUNDS
- C08L51/00—Compositions of graft polymers in which the grafted component is obtained by reactions only involving carbon-to-carbon unsaturated bonds; Compositions of derivatives of such polymers
- C08L51/04—Compositions of graft polymers in which the grafted component is obtained by reactions only involving carbon-to-carbon unsaturated bonds; Compositions of derivatives of such polymers grafted on to rubbers
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- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
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- C08L51/00—Compositions of graft polymers in which the grafted component is obtained by reactions only involving carbon-to-carbon unsaturated bonds; Compositions of derivatives of such polymers
- C08L51/08—Compositions of graft polymers in which the grafted component is obtained by reactions only involving carbon-to-carbon unsaturated bonds; Compositions of derivatives of such polymers grafted on to macromolecular compounds obtained otherwise than by reactions only involving unsaturated carbon-to-carbon bonds
- C08L51/085—Compositions of graft polymers in which the grafted component is obtained by reactions only involving carbon-to-carbon unsaturated bonds; Compositions of derivatives of such polymers grafted on to macromolecular compounds obtained otherwise than by reactions only involving unsaturated carbon-to-carbon bonds on to polysiloxanes
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- C08L55/00—Compositions of homopolymers or copolymers, obtained by polymerisation reactions only involving carbon-to-carbon unsaturated bonds, not provided for in groups C08L23/00 - C08L53/00
- C08L55/02—ABS [Acrylonitrile-Butadiene-Styrene] polymers
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- Compositions Of Macromolecular Compounds (AREA)
Abstract
Description
Claims (19)
- (A) 방향족 (코)폴리(에스테르)카르보네이트 10 내지 88 pbw (조성물의 중량에 대한 중량%),(B) 폴리우레탄, 에틸렌 비닐 아세테이트, 실리콘, 에틸렌-프로필렌 디엔, 에틸렌 프로필렌, 아크릴레이트, 디엔, 및 폴리클로로프렌으로 이루어진 군으로부터 선택된 1종 이상의 고무를 함유하는 그래프트 기재 및 그래프팅된 상을 함유하는 제1 그래프트 (공)중합체 10 내지 88 pbw,(C) 1종 이상의 글리시딜 에스테르 단량체로부터 유도된 반복 단위를 포함하는 선형 글리시딜 에스테르 관능성 중합체 1 내지 20 pbw, 및(D) 폴리(메트)알킬 아크릴레이트 및 폴리오르가노실록산의 상호침투 망상 구조를 포함하는 분자 구조의 코어(core), 및 폴리(메트)아크릴레이트를 함유하는 쉘(shell)을 함유하는 제2 그래프트 (공)중합체 1 내지 20 pbw를 포함하는 열가소성 성형 조성물.
- 제1항에 있어서, 고무가 ASTM D-746-52T에 따라 0℃ 이하의 2차 상전이 온도를 갖는 것인 조성물.
- 제1항에 있어서, 고무가 1,3-디엔의 단일중합체, 1,3-디엔과 1종 이상의 공중합성 단량체의 공중합체 및 혼성중합체로 이루어진 군으로부터 선택된 것인 조성 물.
- 제1항에 있어서, 고무가 가교된 것인 조성물.
- 제1항에 있어서, 제1 그래프트 (공)중합체가 3 내지 50%의 고무 성분을 함유하고, 그래프팅된 상은 49 내지 96%의 중합된 모노비닐리덴 방향족 단량체, 및 1 내지 48%의 중합된 모노에틸렌계 불포화 극성 단량체를 함유하고, 상기 백분율은 제1 그래프트 (공)중합체의 중량에 대한 것인 조성물.
- 제1항에 있어서, 제1 그래프트 (공)중합체가 아크릴로니트릴-부타디엔-스티렌 수지인 조성물.
- 제6항에 있어서, 아크릴로니트릴-부타디엔-스티렌 수지가 괴상 현탁(mass suspension) 중합의 생성물인 조성물.
- 제7항에 있어서, 아크릴로니트릴-부타디엔-스티렌 수지가 폴리부타디엔 함량이 5 내지 20 중량%이고 그의 입자 크기가 0.3 내지 6 마이크로미터의 범위인 것을 특징으로 하는 조성물.
- 제1항에 있어서, 방향족 (코)폴리(에스테르)카르보네이트가 비스페놀 A에 기초한 호모폴리카르보네이트인 조성물.
- 제1항에 있어서, 선형 글리시딜 에스테르가 글리시딜 아크릴레이트 및 글리시딜 메타크릴레이트로 이루어진 군으로부터 선택된 것인 조성물.
- 제1항에 있어서, 글리시딜 에스테르 중합체가 글리시딜 에스테르 단량체로부터 중합된 하나 이상의 반복 단위 및 α-올레핀 단량체로부터 중합된 하나 이상의 반복 단위를 포함하는 것인 조성물.
- 제11항에 있어서, α-올레핀 단량체는 에틸렌, 프로필렌, 1-부텐 및 1-펜텐으로 이루어진 군으로부터 선택된 것인 조성물.
- 제1항에 있어서, 선형 글리시딜 에스테르 관능성 중합체가 비닐 방향족 단량체, 비닐 에스테르 및 C1-20-알킬 (메트)아크릴레이트로 이루어진 군으로부터 선택된 1종 이상으로부터 유도된 반복 단위를 그의 중량에 대해 50% 이하의 양으로 더 함유하는 것인 조성물.
- 제1항에 있어서, 글리시딜 에스테르 관능성 중합체가 올레핀-글리시딜 (메트)아크릴레이트 중합체, 올레핀-비닐 아세테이트-글리시딜 (메트)아크릴레이트 중 합체 및 올레핀-글리시딜 (메트)아크릴레이트-알킬 (메트)아크릴레이트 중합체로 이루어진 군으로부터 선택된 것인 조성물.
- 제14항에 있어서, 글리시딜 에스테르 관능성 중합체가 에틸렌, (메트)아크릴레이트, 및 글리시딜 (메트)아크릴레이트로부터 유도된 구조 단위를 함유하는 것인 조성물.
- 제15항에 있어서, 글리시딜 에스테르 관능성 중합체가 에틸렌/알킬아크릴레이트/글리시딜 메타크릴레이트, 에틸렌/알킬 아크릴레이트/글리시딜 아크릴레이트, 에틸렌/알킬 메타크릴레이트/글리시딜 아크릴레이트, 및 에틸렌/알킬 메타크릴레이트/글리시딜 메타크릴레이트로 이루어진 군으로부터 선택된 삼원공중합체인 조성물.
- 제1항에 있어서, 코어가 폴리부틸 아크릴레이트 및 폴리실록산의 상호침투 망상 구조를 함유하는 것인 조성물.
- 제17항에 있어서, 쉘이 메틸메타크릴레이트로 중합된 것인 조성물.
- 제1항에 있어서, 윤활제, 이형제, 핵형성제(nucleating agent), 대전 방지제, 열 안정화제, 광 안정화제, 가수분해 안정화제, 충전제, 보강제, 착색제, 안 료, 내화제 및 적하 억제제(drip suppressant)로 이루어진 군으로부터 선택된 1종 이상의 성분을 더 함유하는 조성물.
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US11/592,424 US8642700B2 (en) | 2006-11-03 | 2006-11-03 | Thermoplastic composition having low gloss and low temperature impact performance |
US11/592,424 | 2006-11-03 | ||
PCT/US2007/022997 WO2008057355A2 (en) | 2006-11-03 | 2007-10-31 | Thermoplastic composition having low gloss and low temperature impact performance |
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US (1) | US8642700B2 (ko) |
EP (1) | EP2079800B1 (ko) |
JP (1) | JP4987084B2 (ko) |
KR (1) | KR101404907B1 (ko) |
CN (1) | CN101535407B (ko) |
BR (1) | BRPI0718044A2 (ko) |
CA (1) | CA2667888C (ko) |
ES (1) | ES2433685T3 (ko) |
MX (1) | MX2009004637A (ko) |
RU (1) | RU2458088C9 (ko) |
TW (1) | TWI424024B (ko) |
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Families Citing this family (28)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US9193860B2 (en) * | 2007-03-02 | 2015-11-24 | Bayer Materialscience Llc | Thermoplastic molding composition based on AES rubber with low surface gloss |
DE102009005762A1 (de) * | 2008-12-23 | 2010-06-24 | Bayer Materialscience Ag | Schlagzähmodifizierte Polycarbonat-Zusammensetzungen |
KR101145834B1 (ko) | 2008-12-23 | 2012-05-17 | 주식회사 삼양사 | 저광택 열가소성 수지 조성물 |
CN101914261B (zh) * | 2010-08-12 | 2013-03-20 | 河北科技大学 | 聚氨酯油/聚丙烯酸酯胶乳互穿网络聚合物乳液材料及其合成工艺 |
KR101453772B1 (ko) | 2010-10-22 | 2014-10-21 | 제일모직 주식회사 | 폴리카보네이트 수지 조성물 및 이를 이용한 성형품 |
US9293617B2 (en) | 2012-12-10 | 2016-03-22 | Honeywell International Inc. | Copolymer of phase change material for thermal management of PV modules |
JP6387781B2 (ja) * | 2013-11-01 | 2018-09-12 | 日信化学工業株式会社 | 化粧料及びその製造方法 |
US10066102B2 (en) | 2013-11-22 | 2018-09-04 | Trinseo Europe Gmbh | Polycarbonate containing compositions |
CN105814138B (zh) * | 2013-11-22 | 2018-06-01 | 盛禧奥欧洲有限责任公司 | 含聚碳酸酯的组合物 |
EP3387068B1 (en) * | 2015-12-09 | 2020-10-28 | Covestro LLC | Thermoplastic compositions having low gloss and high impact strength |
CN106928694B (zh) * | 2015-12-31 | 2020-04-10 | 万华化学集团股份有限公司 | 一种低光泽度的热塑性聚氨酯组合物及其制备方法和应用 |
CN105802175B (zh) * | 2016-04-08 | 2017-03-15 | 广东优科艾迪高分子材料有限公司 | 聚芳酯‑聚二甲基硅氧烷嵌段共聚物改性的聚碳酸酯及其制备方法 |
EP3844221B1 (en) * | 2018-08-31 | 2023-09-27 | Dupont Polymers, Inc. | Copolyetherester resin formulation |
CN109306169A (zh) * | 2018-09-11 | 2019-02-05 | 铨盛(云浮)新型聚合物有限公司 | 一种杂化有机物和纳米二氧化硅的有机硅阻燃剂及其制备方法 |
KR102363986B1 (ko) | 2018-11-16 | 2022-02-16 | 주식회사 엘지화학 | 코어-쉘 공중합체, 이의 제조방법 및 이를 포함하는 열가소성 수지 조성물 |
WO2020101342A1 (ko) * | 2018-11-16 | 2020-05-22 | 주식회사 엘지화학 | 코어-쉘 공중합체, 이의 제조방법 및 이를 포함하는 열가소성 수지 조성물 |
EP3663340B1 (en) * | 2018-12-03 | 2022-03-16 | Trinseo Europe GmbH | Foams and methods of forming foams of chain extended/branched copolymers of vinylidene substituted aromatic monomers |
CN109762318B (zh) * | 2018-12-30 | 2021-06-29 | 上海锦湖日丽塑料有限公司 | 一种吸能减震性pc/abs合金及其制备方法 |
WO2021138113A1 (en) * | 2020-01-02 | 2021-07-08 | Covestro Llc | Chemical resistant polycarbonate blend compositions |
JP2020073691A (ja) * | 2020-01-17 | 2020-05-14 | コベストロ・エルエルシー | 低光沢性および高衝撃強度の熱可塑性組成物 |
CN112375363B (zh) * | 2020-11-06 | 2022-03-22 | 金发科技股份有限公司 | 一种玻纤增强的聚碳酸酯组合物及其制备方法和应用 |
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CN112375362B (zh) * | 2020-11-06 | 2022-03-22 | 金发科技股份有限公司 | 一种pc/abs组合物及其制备方法和应用 |
CN112480625B (zh) * | 2020-11-06 | 2022-03-22 | 金发科技股份有限公司 | 一种聚酯合金组合物及其制备方法和应用 |
WO2022209415A1 (ja) * | 2021-03-31 | 2022-10-06 | 住化ポリカーボネート株式会社 | 艶消し性ポリカーボネート樹脂組成物 |
CN114133722B (zh) * | 2021-10-26 | 2023-09-19 | 金发科技股份有限公司 | 一种pc复合材料及其制备方法和应用 |
CN114539785B (zh) * | 2022-04-01 | 2023-11-17 | 郑州轻工业大学 | 一种聚氨酯改性的橡胶复合材料、制备方法及其在避雷器复合外套中的应用 |
CN115975366B (zh) * | 2023-01-13 | 2024-02-13 | 佛山市达孚新材料有限公司 | 一种改性聚碳酸酯树脂及其制品和制备方法 |
Citations (4)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US5308894A (en) | 1990-04-12 | 1994-05-03 | The Dow Chemical Company | Polycarbonate/aromatic polyester blends containing an olefinic modifier |
EP1141114A1 (en) * | 1998-12-24 | 2001-10-10 | General Electric Company | Polycarbonate resin composition |
KR20050032099A (ko) * | 2002-07-29 | 2005-04-06 | 바이엘 머티리얼사이언스 아게 | 난연성 폴리카르보네이트 성형 화합물 |
KR100617340B1 (ko) | 2005-07-22 | 2006-08-28 | 제일모직주식회사 | 저광택 난연성 열가소성 수지 조성물 |
Family Cites Families (15)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US4450733A (en) * | 1981-10-05 | 1984-05-29 | Rantapaa Larry A | Pedal extension device |
US4460733A (en) | 1982-11-29 | 1984-07-17 | Mobay Chemical Corporation | Polycarbonate compositions having low gloss values |
US4677162A (en) * | 1983-04-15 | 1987-06-30 | Mobay Corporation | Polycarbonate blends having low gloss |
US4526926A (en) | 1983-04-22 | 1985-07-02 | The Dow Chemical Company | Low gloss carbonate polymer blends |
US4885335A (en) | 1988-12-27 | 1989-12-05 | General Electric Company | Low gloss thermoplastic blends |
US4902743A (en) | 1988-12-27 | 1990-02-20 | General Electric Company | Low gloss thermoplastic blends |
US5026777A (en) | 1989-11-17 | 1991-06-25 | General Electric Company | Low gloss thermoplastic molding compositions |
CA2033903C (en) | 1991-01-10 | 2001-12-18 | Ronald L. Jalbert | Low gloss thermoplastic molding compositions |
EP0519098B1 (en) * | 1991-06-19 | 1995-09-20 | General Electric Company | Aromatic carbonate polymer based blend with low gloss |
US5354796A (en) * | 1992-10-01 | 1994-10-11 | General Electric Company | Low gloss thermoplastic molding compositions |
JP3389644B2 (ja) * | 1993-07-30 | 2003-03-24 | ジェイエスアール株式会社 | 難燃性樹脂組成物 |
US7015261B1 (en) * | 2000-11-17 | 2006-03-21 | Arkema Inc. | Impact modifier combination for polymers |
DE10100591A1 (de) * | 2001-01-09 | 2002-07-11 | Bayer Ag | Phosphorhaltiges Flammschutzmittel und Flammwidrige thermoplastische Formmassen |
US8084550B2 (en) * | 2005-05-23 | 2011-12-27 | Sabic Innovative Plastics Ip B.V. | Low gloss thermoplastic composition |
US7498383B2 (en) * | 2005-07-08 | 2009-03-03 | Sabic Innovative Plastics Ip B.V. | Low gloss thermoplastic composition, method of making, and articles formed therefrom |
-
2006
- 2006-11-03 US US11/592,424 patent/US8642700B2/en active Active
-
2007
- 2007-09-14 TW TW096134339A patent/TWI424024B/zh not_active IP Right Cessation
- 2007-10-31 MX MX2009004637A patent/MX2009004637A/es active IP Right Grant
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- 2007-10-31 WO PCT/US2007/022997 patent/WO2008057355A2/en active Application Filing
- 2007-10-31 EP EP07853046.6A patent/EP2079800B1/en active Active
- 2007-10-31 CN CN2007800410536A patent/CN101535407B/zh active Active
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- 2007-10-31 RU RU2009120892/05A patent/RU2458088C9/ru not_active IP Right Cessation
- 2007-10-31 ES ES07853046T patent/ES2433685T3/es active Active
Patent Citations (4)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US5308894A (en) | 1990-04-12 | 1994-05-03 | The Dow Chemical Company | Polycarbonate/aromatic polyester blends containing an olefinic modifier |
EP1141114A1 (en) * | 1998-12-24 | 2001-10-10 | General Electric Company | Polycarbonate resin composition |
KR20050032099A (ko) * | 2002-07-29 | 2005-04-06 | 바이엘 머티리얼사이언스 아게 | 난연성 폴리카르보네이트 성형 화합물 |
KR100617340B1 (ko) | 2005-07-22 | 2006-08-28 | 제일모직주식회사 | 저광택 난연성 열가소성 수지 조성물 |
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WO2008057355A2 (en) | 2008-05-15 |
EP2079800B1 (en) | 2013-09-04 |
EP2079800A2 (en) | 2009-07-22 |
TWI424024B (zh) | 2014-01-21 |
TW200831605A (en) | 2008-08-01 |
RU2009120892A (ru) | 2010-12-10 |
RU2458088C9 (ru) | 2013-04-10 |
KR20090086204A (ko) | 2009-08-11 |
CA2667888C (en) | 2015-10-06 |
MX2009004637A (es) | 2009-05-15 |
JP2010509434A (ja) | 2010-03-25 |
CA2667888A1 (en) | 2008-05-15 |
BRPI0718044A2 (pt) | 2014-04-15 |
US20080108751A1 (en) | 2008-05-08 |
RU2458088C2 (ru) | 2012-08-10 |
CN101535407A (zh) | 2009-09-16 |
US8642700B2 (en) | 2014-02-04 |
CN101535407B (zh) | 2012-05-30 |
ES2433685T3 (es) | 2013-12-12 |
WO2008057355A3 (en) | 2008-07-31 |
JP4987084B2 (ja) | 2012-07-25 |
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