KR101923256B1 - 폴리카보네이트 수지 조성물 펠릿 및 그 제조 방법 - Google Patents
폴리카보네이트 수지 조성물 펠릿 및 그 제조 방법 Download PDFInfo
- Publication number
- KR101923256B1 KR101923256B1 KR1020147017611A KR20147017611A KR101923256B1 KR 101923256 B1 KR101923256 B1 KR 101923256B1 KR 1020147017611 A KR1020147017611 A KR 1020147017611A KR 20147017611 A KR20147017611 A KR 20147017611A KR 101923256 B1 KR101923256 B1 KR 101923256B1
- Authority
- KR
- South Korea
- Prior art keywords
- group
- polycarbonate resin
- resin composition
- mass
- light transmittance
- 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.)
- Active
Links
- 239000004431 polycarbonate resin Substances 0.000 title claims description 62
- 239000008188 pellet Substances 0.000 title claims description 54
- 229920005668 polycarbonate resin Polymers 0.000 title claims description 51
- 239000000203 mixture Substances 0.000 title claims description 48
- 238000000034 method Methods 0.000 title claims description 26
- 238000004519 manufacturing process Methods 0.000 title claims description 8
- 238000002834 transmittance Methods 0.000 claims abstract description 58
- YMWUJEATGCHHMB-UHFFFAOYSA-N Dichloromethane Chemical compound ClCCl YMWUJEATGCHHMB-UHFFFAOYSA-N 0.000 claims abstract description 55
- 230000003287 optical effect Effects 0.000 claims abstract description 11
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N silicon dioxide Inorganic materials O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 claims abstract description 8
- -1 fatty acid monoglycerides Chemical class 0.000 claims description 55
- 125000004432 carbon atom Chemical group C* 0.000 claims description 34
- 229920005989 resin Polymers 0.000 claims description 32
- 239000011347 resin Substances 0.000 claims description 32
- 150000001875 compounds Chemical class 0.000 claims description 28
- 238000004898 kneading Methods 0.000 claims description 24
- 125000000217 alkyl group Chemical group 0.000 claims description 20
- 239000000126 substance Substances 0.000 claims description 19
- LYCAIKOWRPUZTN-UHFFFAOYSA-N Ethylene glycol Chemical compound OCCO LYCAIKOWRPUZTN-UHFFFAOYSA-N 0.000 claims description 15
- 229920000178 Acrylic resin Polymers 0.000 claims description 11
- 239000004925 Acrylic resin Substances 0.000 claims description 11
- 238000000465 moulding Methods 0.000 claims description 11
- 239000003963 antioxidant agent Substances 0.000 claims description 10
- 239000003795 chemical substances by application Substances 0.000 claims description 10
- 229920001296 polysiloxane Polymers 0.000 claims description 10
- 125000002723 alicyclic group Chemical group 0.000 claims description 9
- 239000004593 Epoxy Substances 0.000 claims description 8
- 230000003078 antioxidant effect Effects 0.000 claims description 8
- 235000014113 dietary fatty acids Nutrition 0.000 claims description 8
- 239000000194 fatty acid Substances 0.000 claims description 8
- 229930195729 fatty acid Natural products 0.000 claims description 8
- WGCNASOHLSPBMP-UHFFFAOYSA-N hydroxyacetaldehyde Natural products OCC=O WGCNASOHLSPBMP-UHFFFAOYSA-N 0.000 claims description 8
- 125000003118 aryl group Chemical group 0.000 claims description 7
- 125000000524 functional group Chemical group 0.000 claims description 7
- 229920003229 poly(methyl methacrylate) Polymers 0.000 claims description 7
- 239000004926 polymethyl methacrylate Substances 0.000 claims description 7
- 125000003545 alkoxy group Chemical group 0.000 claims description 6
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 claims description 6
- 125000000391 vinyl group Chemical group [H]C([*])=C([H])[H] 0.000 claims description 6
- 229920003171 Poly (ethylene oxide) Polymers 0.000 claims description 5
- OJMIONKXNSYLSR-UHFFFAOYSA-N phosphorous acid Chemical class OP(O)O OJMIONKXNSYLSR-UHFFFAOYSA-N 0.000 claims description 4
- YZCKVEUIGOORGS-OUBTZVSYSA-N Deuterium Chemical compound [2H] YZCKVEUIGOORGS-OUBTZVSYSA-N 0.000 claims description 3
- VBICKXHEKHSIBG-UHFFFAOYSA-N beta-monoglyceryl stearate Natural products CCCCCCCCCCCCCCCCCC(=O)OCC(O)CO VBICKXHEKHSIBG-UHFFFAOYSA-N 0.000 claims description 3
- 229910052805 deuterium Inorganic materials 0.000 claims description 3
- 229910052736 halogen Inorganic materials 0.000 claims description 3
- 150000002367 halogens Chemical class 0.000 claims description 3
- 230000007935 neutral effect Effects 0.000 claims description 2
- 239000011521 glass Substances 0.000 abstract description 5
- 239000010453 quartz Substances 0.000 abstract description 5
- 239000004417 polycarbonate Substances 0.000 description 26
- 239000000243 solution Substances 0.000 description 26
- 150000002009 diols Chemical class 0.000 description 18
- 229920001577 copolymer Polymers 0.000 description 15
- 238000005259 measurement Methods 0.000 description 12
- 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 description 11
- 229920000402 bisphenol A polycarbonate polymer Polymers 0.000 description 11
- 238000002156 mixing Methods 0.000 description 11
- 125000002947 alkylene group Chemical group 0.000 description 9
- 230000000694 effects Effects 0.000 description 7
- ISWSIDIOOBJBQZ-UHFFFAOYSA-N Phenol Chemical compound OC1=CC=CC=C1 ISWSIDIOOBJBQZ-UHFFFAOYSA-N 0.000 description 6
- ATUOYWHBWRKTHZ-UHFFFAOYSA-N Propane Chemical compound CCC ATUOYWHBWRKTHZ-UHFFFAOYSA-N 0.000 description 6
- ZMANZCXQSJIPKH-UHFFFAOYSA-N Triethylamine Chemical compound CCN(CC)CC ZMANZCXQSJIPKH-UHFFFAOYSA-N 0.000 description 6
- 230000000052 comparative effect Effects 0.000 description 6
- FJKROLUGYXJWQN-UHFFFAOYSA-N 4-hydroxybenzoic acid Chemical compound OC(=O)C1=CC=C(O)C=C1 FJKROLUGYXJWQN-UHFFFAOYSA-N 0.000 description 5
- 125000001118 alkylidene group Chemical group 0.000 description 5
- 239000002994 raw material Substances 0.000 description 5
- 239000004215 Carbon black (E152) Substances 0.000 description 4
- OAICVXFJPJFONN-UHFFFAOYSA-N Phosphorus Chemical compound [P] OAICVXFJPJFONN-UHFFFAOYSA-N 0.000 description 4
- 239000000654 additive Substances 0.000 description 4
- 239000003054 catalyst Substances 0.000 description 4
- 238000007334 copolymerization reaction Methods 0.000 description 4
- 125000002993 cycloalkylene group Chemical group 0.000 description 4
- 125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 description 4
- 150000004665 fatty acids Chemical class 0.000 description 4
- 229930195733 hydrocarbon Natural products 0.000 description 4
- 150000002430 hydrocarbons Chemical group 0.000 description 4
- 125000005027 hydroxyaryl group Chemical group 0.000 description 4
- 238000002347 injection Methods 0.000 description 4
- 239000007924 injection Substances 0.000 description 4
- 229910052698 phosphorus Inorganic materials 0.000 description 4
- 239000011574 phosphorus Substances 0.000 description 4
- LDVVTQMJQSCDMK-UHFFFAOYSA-N 1,3-dihydroxypropan-2-yl formate Chemical compound OCC(CO)OC=O LDVVTQMJQSCDMK-UHFFFAOYSA-N 0.000 description 3
- UHOVQNZJYSORNB-UHFFFAOYSA-N Benzene Chemical compound C1=CC=CC=C1 UHOVQNZJYSORNB-UHFFFAOYSA-N 0.000 description 3
- JKIJEFPNVSHHEI-UHFFFAOYSA-N Phenol, 2,4-bis(1,1-dimethylethyl)-, phosphite (3:1) Chemical compound CC(C)(C)C1=CC(C(C)(C)C)=CC=C1OP(OC=1C(=CC(=CC=1)C(C)(C)C)C(C)(C)C)OC1=CC=C(C(C)(C)C)C=C1C(C)(C)C JKIJEFPNVSHHEI-UHFFFAOYSA-N 0.000 description 3
- 239000004721 Polyphenylene oxide Substances 0.000 description 3
- HEMHJVSKTPXQMS-UHFFFAOYSA-M Sodium hydroxide Chemical compound [OH-].[Na+] HEMHJVSKTPXQMS-UHFFFAOYSA-M 0.000 description 3
- YXFVVABEGXRONW-UHFFFAOYSA-N Toluene Chemical compound CC1=CC=CC=C1 YXFVVABEGXRONW-UHFFFAOYSA-N 0.000 description 3
- 239000007983 Tris buffer Substances 0.000 description 3
- 230000006866 deterioration Effects 0.000 description 3
- 238000001125 extrusion Methods 0.000 description 3
- 239000004973 liquid crystal related substance Substances 0.000 description 3
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 description 3
- 229920000570 polyether Polymers 0.000 description 3
- 239000001294 propane Substances 0.000 description 3
- 239000011342 resin composition Substances 0.000 description 3
- 150000003512 tertiary amines Chemical class 0.000 description 3
- HVLLSGMXQDNUAL-UHFFFAOYSA-N triphenyl phosphite Chemical compound C=1C=CC=CC=1OP(OC=1C=CC=CC=1)OC1=CC=CC=C1 HVLLSGMXQDNUAL-UHFFFAOYSA-N 0.000 description 3
- PEXOFOFLXOCMDX-UHFFFAOYSA-N tritridecyl phosphite Chemical compound CCCCCCCCCCCCCOP(OCCCCCCCCCCCCC)OCCCCCCCCCCCCC PEXOFOFLXOCMDX-UHFFFAOYSA-N 0.000 description 3
- RNFJDJUURJAICM-UHFFFAOYSA-N 2,2,4,4,6,6-hexaphenoxy-1,3,5-triaza-2$l^{5},4$l^{5},6$l^{5}-triphosphacyclohexa-1,3,5-triene Chemical compound N=1P(OC=2C=CC=CC=2)(OC=2C=CC=CC=2)=NP(OC=2C=CC=CC=2)(OC=2C=CC=CC=2)=NP=1(OC=1C=CC=CC=1)OC1=CC=CC=C1 RNFJDJUURJAICM-UHFFFAOYSA-N 0.000 description 2
- ICKWICRCANNIBI-UHFFFAOYSA-N 2,4-di-tert-butylphenol Chemical compound CC(C)(C)C1=CC=C(O)C(C(C)(C)C)=C1 ICKWICRCANNIBI-UHFFFAOYSA-N 0.000 description 2
- NGNBDVOYPDDBFK-UHFFFAOYSA-N 2-[2,4-di(pentan-2-yl)phenoxy]acetyl chloride Chemical compound CCCC(C)C1=CC=C(OCC(Cl)=O)C(C(C)CCC)=C1 NGNBDVOYPDDBFK-UHFFFAOYSA-N 0.000 description 2
- GJYCVCVHRSWLNY-UHFFFAOYSA-N 2-butylphenol Chemical compound CCCCC1=CC=CC=C1O GJYCVCVHRSWLNY-UHFFFAOYSA-N 0.000 description 2
- VPWNQTHUCYMVMZ-UHFFFAOYSA-N 4,4'-sulfonyldiphenol Chemical class C1=CC(O)=CC=C1S(=O)(=O)C1=CC=C(O)C=C1 VPWNQTHUCYMVMZ-UHFFFAOYSA-N 0.000 description 2
- KWOLFJPFCHCOCG-UHFFFAOYSA-N Acetophenone Chemical compound CC(=O)C1=CC=CC=C1 KWOLFJPFCHCOCG-UHFFFAOYSA-N 0.000 description 2
- 229930185605 Bisphenol Natural products 0.000 description 2
- KAKZBPTYRLMSJV-UHFFFAOYSA-N Butadiene Chemical compound C=CC=C KAKZBPTYRLMSJV-UHFFFAOYSA-N 0.000 description 2
- RTZKZFJDLAIYFH-UHFFFAOYSA-N Diethyl ether Chemical compound CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 description 2
- 101000870363 Oryctolagus cuniculus Glutathione S-transferase Yc Proteins 0.000 description 2
- YGYAWVDWMABLBF-UHFFFAOYSA-N Phosgene Chemical class ClC(Cl)=O YGYAWVDWMABLBF-UHFFFAOYSA-N 0.000 description 2
- JUJWROOIHBZHMG-UHFFFAOYSA-N Pyridine Chemical compound C1=CC=NC=C1 JUJWROOIHBZHMG-UHFFFAOYSA-N 0.000 description 2
- PPBRXRYQALVLMV-UHFFFAOYSA-N Styrene Chemical compound C=CC1=CC=CC=C1 PPBRXRYQALVLMV-UHFFFAOYSA-N 0.000 description 2
- BZGAQVCARMIDQA-UHFFFAOYSA-N [4-[2-(4-hydroxyphenyl)propan-2-yl]phenyl] tetradecyl hydrogen phosphite Chemical compound C1=CC(OP(O)OCCCCCCCCCCCCCC)=CC=C1C(C)(C)C1=CC=C(O)C=C1 BZGAQVCARMIDQA-UHFFFAOYSA-N 0.000 description 2
- NIXOWILDQLNWCW-UHFFFAOYSA-N acrylic acid group Chemical group C(C=C)(=O)O NIXOWILDQLNWCW-UHFFFAOYSA-N 0.000 description 2
- 150000001335 aliphatic alkanes Chemical class 0.000 description 2
- 239000003513 alkali Substances 0.000 description 2
- 125000005907 alkyl ester group Chemical group 0.000 description 2
- 230000003064 anti-oxidating effect Effects 0.000 description 2
- 125000003710 aryl alkyl group Chemical group 0.000 description 2
- 230000015572 biosynthetic process Effects 0.000 description 2
- LLEMOWNGBBNAJR-UHFFFAOYSA-N biphenyl-2-ol Chemical compound OC1=CC=CC=C1C1=CC=CC=C1 LLEMOWNGBBNAJR-UHFFFAOYSA-N 0.000 description 2
- YXVFYQXJAXKLAK-UHFFFAOYSA-N biphenyl-4-ol Chemical compound C1=CC(O)=CC=C1C1=CC=CC=C1 YXVFYQXJAXKLAK-UHFFFAOYSA-N 0.000 description 2
- PXKLMJQFEQBVLD-UHFFFAOYSA-N bisphenol F Chemical compound C1=CC(O)=CC=C1CC1=CC=C(O)C=C1 PXKLMJQFEQBVLD-UHFFFAOYSA-N 0.000 description 2
- 239000006085 branching agent Substances 0.000 description 2
- 230000015556 catabolic process Effects 0.000 description 2
- 230000008859 change Effects 0.000 description 2
- MVPPADPHJFYWMZ-UHFFFAOYSA-N chlorobenzene Chemical compound ClC1=CC=CC=C1 MVPPADPHJFYWMZ-UHFFFAOYSA-N 0.000 description 2
- 238000004140 cleaning Methods 0.000 description 2
- 150000001924 cycloalkanes Chemical class 0.000 description 2
- 238000006731 degradation reaction Methods 0.000 description 2
- 239000000428 dust Substances 0.000 description 2
- 125000003700 epoxy group Chemical group 0.000 description 2
- 238000011156 evaluation Methods 0.000 description 2
- 239000003063 flame retardant Substances 0.000 description 2
- 125000004435 hydrogen atom Chemical group [H]* 0.000 description 2
- 238000010348 incorporation Methods 0.000 description 2
- 238000001746 injection moulding Methods 0.000 description 2
- 125000001449 isopropyl group Chemical group [H]C([H])([H])C([H])(*)C([H])([H])[H] 0.000 description 2
- 125000004123 n-propyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])* 0.000 description 2
- QWVGKYWNOKOFNN-UHFFFAOYSA-N o-cresol Chemical compound CC1=CC=CC=C1O QWVGKYWNOKOFNN-UHFFFAOYSA-N 0.000 description 2
- 239000003960 organic solvent Substances 0.000 description 2
- QBDSZLJBMIMQRS-UHFFFAOYSA-N p-Cumylphenol Chemical compound C=1C=C(O)C=CC=1C(C)(C)C1=CC=CC=C1 QBDSZLJBMIMQRS-UHFFFAOYSA-N 0.000 description 2
- IWDCLRJOBJJRNH-UHFFFAOYSA-N p-cresol Chemical compound CC1=CC=C(O)C=C1 IWDCLRJOBJJRNH-UHFFFAOYSA-N 0.000 description 2
- NKTOLZVEWDHZMU-UHFFFAOYSA-N p-cumyl phenol Natural products CC1=CC=C(C)C(O)=C1 NKTOLZVEWDHZMU-UHFFFAOYSA-N 0.000 description 2
- 125000004817 pentamethylene group Chemical group [H]C([H])([*:2])C([H])([H])C([H])([H])C([H])([H])C([H])([H])[*:1] 0.000 description 2
- 239000002530 phenolic antioxidant Substances 0.000 description 2
- 150000002989 phenols Chemical class 0.000 description 2
- 150000004714 phosphonium salts Chemical group 0.000 description 2
- 229910000073 phosphorus hydride Inorganic materials 0.000 description 2
- 229920000515 polycarbonate Polymers 0.000 description 2
- 150000003242 quaternary ammonium salts Chemical class 0.000 description 2
- 239000003381 stabilizer Substances 0.000 description 2
- NHGXDBSUJJNIRV-UHFFFAOYSA-M tetrabutylammonium chloride Chemical compound [Cl-].CCCC[N+](CCCC)(CCCC)CCCC NHGXDBSUJJNIRV-UHFFFAOYSA-M 0.000 description 2
- VZGDMQKNWNREIO-UHFFFAOYSA-N tetrachloromethane Chemical compound ClC(Cl)(Cl)Cl VZGDMQKNWNREIO-UHFFFAOYSA-N 0.000 description 2
- ARCGXLSVLAOJQL-UHFFFAOYSA-N trimellitic acid Chemical group OC(=O)C1=CC=C(C(O)=O)C(C(O)=O)=C1 ARCGXLSVLAOJQL-UHFFFAOYSA-N 0.000 description 2
- RIOQSEWOXXDEQQ-UHFFFAOYSA-N triphenylphosphine Chemical compound C1=CC=CC=C1P(C=1C=CC=CC=1)C1=CC=CC=C1 RIOQSEWOXXDEQQ-UHFFFAOYSA-N 0.000 description 2
- KYLUAQBYONVMCP-UHFFFAOYSA-N (2-methylphenyl)phosphane Chemical compound CC1=CC=CC=C1P KYLUAQBYONVMCP-UHFFFAOYSA-N 0.000 description 1
- JSODTDJIRKWSON-UHFFFAOYSA-N (2-tert-butyl-5-methylphenoxy)-dihydroxy-di(tridecyl)-lambda5-phosphane Chemical compound CCCCCCCCCCCCCP(O)(O)(CCCCCCCCCCCCC)OC1=CC(C)=CC=C1C(C)(C)C JSODTDJIRKWSON-UHFFFAOYSA-N 0.000 description 1
- MEKJIUITLNIMMR-UHFFFAOYSA-N 1,1,1,2-tetrachloroethane;1,1,2,2-tetrachloroethane Chemical compound ClCC(Cl)(Cl)Cl.ClC(Cl)C(Cl)Cl MEKJIUITLNIMMR-UHFFFAOYSA-N 0.000 description 1
- KLUSIGFSJQSFKX-UHFFFAOYSA-N 1,1,1-trichloroethane;1,1,2-trichloroethane Chemical compound CC(Cl)(Cl)Cl.ClCC(Cl)Cl KLUSIGFSJQSFKX-UHFFFAOYSA-N 0.000 description 1
- HCNHNBLSNVSJTJ-UHFFFAOYSA-N 1,1-Bis(4-hydroxyphenyl)ethane Chemical compound C=1C=C(O)C=CC=1C(C)C1=CC=C(O)C=C1 HCNHNBLSNVSJTJ-UHFFFAOYSA-N 0.000 description 1
- NUKLDTSTOVGVDB-UHFFFAOYSA-N 1,1-dichloroethane;1,2-dichloroethane Chemical compound CC(Cl)Cl.ClCCCl NUKLDTSTOVGVDB-UHFFFAOYSA-N 0.000 description 1
- NTFMNNZPXYHYNY-UHFFFAOYSA-N 1,2-bis(4-hydroxyphenyl)-10h-anthracen-9-one Chemical compound C1=CC(O)=CC=C1C1=CC=C(CC=2C(=CC=CC=2)C2=O)C2=C1C1=CC=C(O)C=C1 NTFMNNZPXYHYNY-UHFFFAOYSA-N 0.000 description 1
- VNQNXQYZMPJLQX-UHFFFAOYSA-N 1,3,5-tris[(3,5-ditert-butyl-4-hydroxyphenyl)methyl]-1,3,5-triazinane-2,4,6-trione Chemical compound CC(C)(C)C1=C(O)C(C(C)(C)C)=CC(CN2C(N(CC=3C=C(C(O)=C(C=3)C(C)(C)C)C(C)(C)C)C(=O)N(CC=3C=C(C(O)=C(C=3)C(C)(C)C)C(C)(C)C)C2=O)=O)=C1 VNQNXQYZMPJLQX-UHFFFAOYSA-N 0.000 description 1
- XYXJKPCGSGVSBO-UHFFFAOYSA-N 1,3,5-tris[(4-tert-butyl-3-hydroxy-2,6-dimethylphenyl)methyl]-1,3,5-triazinane-2,4,6-trione Chemical compound CC1=CC(C(C)(C)C)=C(O)C(C)=C1CN1C(=O)N(CC=2C(=C(O)C(=CC=2C)C(C)(C)C)C)C(=O)N(CC=2C(=C(O)C(=CC=2C)C(C)(C)C)C)C1=O XYXJKPCGSGVSBO-UHFFFAOYSA-N 0.000 description 1
- FGYJSJUSODGXAR-UHFFFAOYSA-N 1,3,7,9-tetratert-butyl-11-octoxy-5h-benzo[d][1,3,2]benzodioxaphosphocine Chemical compound C1C2=CC(C(C)(C)C)=CC(C(C)(C)C)=C2OP(OCCCCCCCC)OC2=C1C=C(C(C)(C)C)C=C2C(C)(C)C FGYJSJUSODGXAR-UHFFFAOYSA-N 0.000 description 1
- KGRVJHAUYBGFFP-UHFFFAOYSA-N 2,2'-Methylenebis(4-methyl-6-tert-butylphenol) Chemical compound CC(C)(C)C1=CC(C)=CC(CC=2C(=C(C=C(C)C=2)C(C)(C)C)O)=C1O KGRVJHAUYBGFFP-UHFFFAOYSA-N 0.000 description 1
- BSWWXRFVMJHFBN-UHFFFAOYSA-N 2,4,6-tribromophenol Chemical compound OC1=C(Br)C=C(Br)C=C1Br BSWWXRFVMJHFBN-UHFFFAOYSA-N 0.000 description 1
- KDPQUXLWQYXMCE-UHFFFAOYSA-N 2,5-bis(2-phenylpropan-2-yl)phenol Chemical compound C=1C=C(C(C)(C)C=2C=CC=CC=2)C(O)=CC=1C(C)(C)C1=CC=CC=C1 KDPQUXLWQYXMCE-UHFFFAOYSA-N 0.000 description 1
- KDBZVULQVCUNNA-UHFFFAOYSA-N 2,5-di-tert-butylphenol Chemical compound CC(C)(C)C1=CC=C(C(C)(C)C)C(O)=C1 KDBZVULQVCUNNA-UHFFFAOYSA-N 0.000 description 1
- YAGPRJYCDKGWJR-UHFFFAOYSA-N 2-(2,4,8,10-tetratert-butylbenzo[d][1,3,2]benzodioxaphosphepin-6-yl)oxy-n,n-bis[2-(2,4,8,10-tetratert-butylbenzo[d][1,3,2]benzodioxaphosphepin-6-yl)oxyethyl]ethanamine Chemical compound O1C2=C(C(C)(C)C)C=C(C(C)(C)C)C=C2C2=CC(C(C)(C)C)=CC(C(C)(C)C)=C2OP1OCCN(CCOP1OC2=C(C=C(C=C2C=2C=C(C=C(C=2O1)C(C)(C)C)C(C)(C)C)C(C)(C)C)C(C)(C)C)CCOP(OC1=C(C=C(C=C11)C(C)(C)C)C(C)(C)C)OC2=C1C=C(C(C)(C)C)C=C2C(C)(C)C YAGPRJYCDKGWJR-UHFFFAOYSA-N 0.000 description 1
- NFIDBGJMFKNGGQ-UHFFFAOYSA-N 2-(2-methylpropyl)phenol Chemical compound CC(C)CC1=CC=CC=C1O NFIDBGJMFKNGGQ-UHFFFAOYSA-N 0.000 description 1
- CJWNFAKWHDOUKL-UHFFFAOYSA-N 2-(2-phenylpropan-2-yl)phenol Chemical compound C=1C=CC=C(O)C=1C(C)(C)C1=CC=CC=C1 CJWNFAKWHDOUKL-UHFFFAOYSA-N 0.000 description 1
- VADKRMSMGWJZCF-UHFFFAOYSA-N 2-bromophenol Chemical compound OC1=CC=CC=C1Br VADKRMSMGWJZCF-UHFFFAOYSA-N 0.000 description 1
- XBQRPFBBTWXIFI-UHFFFAOYSA-N 2-chloro-4-[2-(3-chloro-4-hydroxyphenyl)propan-2-yl]phenol Chemical compound C=1C=C(O)C(Cl)=CC=1C(C)(C)C1=CC=C(O)C(Cl)=C1 XBQRPFBBTWXIFI-UHFFFAOYSA-N 0.000 description 1
- MVRPPTGLVPEMPI-UHFFFAOYSA-N 2-cyclohexylphenol Chemical compound OC1=CC=CC=C1C1CCCCC1 MVRPPTGLVPEMPI-UHFFFAOYSA-N 0.000 description 1
- XKZGIJICHCVXFV-UHFFFAOYSA-N 2-ethylhexyl diphenyl phosphite Chemical compound C=1C=CC=CC=1OP(OCC(CC)CCCC)OC1=CC=CC=C1 XKZGIJICHCVXFV-UHFFFAOYSA-N 0.000 description 1
- NTRXCTZXSALJEY-UHFFFAOYSA-N 2-naphthalen-1-ylphenol Chemical compound OC1=CC=CC=C1C1=CC=CC2=CC=CC=C12 NTRXCTZXSALJEY-UHFFFAOYSA-N 0.000 description 1
- MEEKGULDSDXFCN-UHFFFAOYSA-N 2-pentylphenol Chemical compound CCCCCC1=CC=CC=C1O MEEKGULDSDXFCN-UHFFFAOYSA-N 0.000 description 1
- YMTYZTXUZLQUSF-UHFFFAOYSA-N 3,3'-Dimethylbisphenol A Chemical compound C1=C(O)C(C)=CC(C(C)(C)C=2C=C(C)C(O)=CC=2)=C1 YMTYZTXUZLQUSF-UHFFFAOYSA-N 0.000 description 1
- CKNCVRMXCLUOJI-UHFFFAOYSA-N 3,3'-dibromobisphenol A Chemical compound C=1C=C(O)C(Br)=CC=1C(C)(C)C1=CC=C(O)C(Br)=C1 CKNCVRMXCLUOJI-UHFFFAOYSA-N 0.000 description 1
- SQQOWYUPNYZZPI-UHFFFAOYSA-N 3,5-bis(2-phenylpropan-2-yl)phenol Chemical compound C=1C(O)=CC(C(C)(C)C=2C=CC=CC=2)=CC=1C(C)(C)C1=CC=CC=C1 SQQOWYUPNYZZPI-UHFFFAOYSA-N 0.000 description 1
- ZDWSNKPLZUXBPE-UHFFFAOYSA-N 3,5-ditert-butylphenol Chemical compound CC(C)(C)C1=CC(O)=CC(C(C)(C)C)=C1 ZDWSNKPLZUXBPE-UHFFFAOYSA-N 0.000 description 1
- SSADPHQCUURWSW-UHFFFAOYSA-N 3,9-bis(2,6-ditert-butyl-4-methylphenoxy)-2,4,8,10-tetraoxa-3,9-diphosphaspiro[5.5]undecane Chemical compound CC(C)(C)C1=CC(C)=CC(C(C)(C)C)=C1OP1OCC2(COP(OC=3C(=CC(C)=CC=3C(C)(C)C)C(C)(C)C)OC2)CO1 SSADPHQCUURWSW-UHFFFAOYSA-N 0.000 description 1
- WBWXVCMXGYSMQA-UHFFFAOYSA-N 3,9-bis[2,4-bis(2-phenylpropan-2-yl)phenoxy]-2,4,8,10-tetraoxa-3,9-diphosphaspiro[5.5]undecane Chemical compound C=1C=C(OP2OCC3(CO2)COP(OC=2C(=CC(=CC=2)C(C)(C)C=2C=CC=CC=2)C(C)(C)C=2C=CC=CC=2)OC3)C(C(C)(C)C=2C=CC=CC=2)=CC=1C(C)(C)C1=CC=CC=C1 WBWXVCMXGYSMQA-UHFFFAOYSA-N 0.000 description 1
- ZKSISJGIJFEBMS-UHFFFAOYSA-N 3-(2-methylpropyl)phenol Chemical compound CC(C)CC1=CC=CC(O)=C1 ZKSISJGIJFEBMS-UHFFFAOYSA-N 0.000 description 1
- PARGHORKDQHVPM-UHFFFAOYSA-N 3-(2-phenylpropan-2-yl)phenol Chemical compound C=1C=CC(O)=CC=1C(C)(C)C1=CC=CC=C1 PARGHORKDQHVPM-UHFFFAOYSA-N 0.000 description 1
- MQSXUKPGWMJYBT-UHFFFAOYSA-N 3-butylphenol Chemical compound CCCCC1=CC=CC(O)=C1 MQSXUKPGWMJYBT-UHFFFAOYSA-N 0.000 description 1
- CRIQSWIRYKZJAV-UHFFFAOYSA-N 3-hexylphenol Chemical compound CCCCCCC1=CC=CC(O)=C1 CRIQSWIRYKZJAV-UHFFFAOYSA-N 0.000 description 1
- MFZDWVIWDAFDRL-UHFFFAOYSA-N 3-naphthalen-1-ylphenol Chemical compound OC1=CC=CC(C=2C3=CC=CC=C3C=CC=2)=C1 MFZDWVIWDAFDRL-UHFFFAOYSA-N 0.000 description 1
- QWGLNWHWBCINBS-UHFFFAOYSA-N 3-nonylphenol Chemical compound CCCCCCCCCC1=CC=CC(O)=C1 QWGLNWHWBCINBS-UHFFFAOYSA-N 0.000 description 1
- YNNMNWHCQGBNFH-UHFFFAOYSA-N 3-tert-butyl-4-[1-(2-tert-butyl-4-hydroxyphenyl)propyl]phenol Chemical compound C=1C=C(O)C=C(C(C)(C)C)C=1C(CC)C1=CC=C(O)C=C1C(C)(C)C YNNMNWHCQGBNFH-UHFFFAOYSA-N 0.000 description 1
- VWGKEVWFBOUAND-UHFFFAOYSA-N 4,4'-thiodiphenol Chemical compound C1=CC(O)=CC=C1SC1=CC=C(O)C=C1 VWGKEVWFBOUAND-UHFFFAOYSA-N 0.000 description 1
- KZMYFIUFUAOZHP-UHFFFAOYSA-N 4-(1-adamantyl)phenol Chemical compound C1=CC(O)=CC=C1C1(C2)CC(C3)CC2CC3C1 KZMYFIUFUAOZHP-UHFFFAOYSA-N 0.000 description 1
- RQCACQIALULDSK-UHFFFAOYSA-N 4-(4-hydroxyphenyl)sulfinylphenol Chemical compound C1=CC(O)=CC=C1S(=O)C1=CC=C(O)C=C1 RQCACQIALULDSK-UHFFFAOYSA-N 0.000 description 1
- BATCUENAARTUKW-UHFFFAOYSA-N 4-[(4-hydroxyphenyl)-diphenylmethyl]phenol Chemical compound C1=CC(O)=CC=C1C(C=1C=CC(O)=CC=1)(C=1C=CC=CC=1)C1=CC=CC=C1 BATCUENAARTUKW-UHFFFAOYSA-N 0.000 description 1
- QHSCVNPSSKNMQL-UHFFFAOYSA-N 4-[(4-hydroxyphenyl)-naphthalen-1-ylmethyl]phenol Chemical compound C1=CC(O)=CC=C1C(C=1C2=CC=CC=C2C=CC=1)C1=CC=C(O)C=C1 QHSCVNPSSKNMQL-UHFFFAOYSA-N 0.000 description 1
- BRPSWMCDEYMRPE-UHFFFAOYSA-N 4-[1,1-bis(4-hydroxyphenyl)ethyl]phenol Chemical compound C=1C=C(O)C=CC=1C(C=1C=CC(O)=CC=1)(C)C1=CC=C(O)C=C1 BRPSWMCDEYMRPE-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
- OQXLHLKXTVFCKC-UHFFFAOYSA-N 4-[1-(4-hydroxyphenyl)-6-methylcyclohexa-2,4-dien-1-yl]phenol Chemical compound CC1C=CC=CC1(C=1C=CC(O)=CC=1)C1=CC=C(O)C=C1 OQXLHLKXTVFCKC-UHFFFAOYSA-N 0.000 description 1
- OVVCSFQRAXVPGT-UHFFFAOYSA-N 4-[1-(4-hydroxyphenyl)cyclopentyl]phenol Chemical compound C1=CC(O)=CC=C1C1(C=2C=CC(O)=CC=2)CCCC1 OVVCSFQRAXVPGT-UHFFFAOYSA-N 0.000 description 1
- WEFHJJXWZHDCCM-UHFFFAOYSA-N 4-[2-(4-hydroxyphenyl)-2-adamantyl]phenol Chemical compound C1=CC(O)=CC=C1C1(C=2C=CC(O)=CC=2)C(C2)CC3CC2CC1C3 WEFHJJXWZHDCCM-UHFFFAOYSA-N 0.000 description 1
- QHJPJZROUNGTRJ-UHFFFAOYSA-N 4-[2-(4-hydroxyphenyl)octan-2-yl]phenol Chemical compound C=1C=C(O)C=CC=1C(C)(CCCCCC)C1=CC=C(O)C=C1 QHJPJZROUNGTRJ-UHFFFAOYSA-N 0.000 description 1
- WXYSZTISEJBRHW-UHFFFAOYSA-N 4-[2-[4-[1,1-bis(4-hydroxyphenyl)ethyl]phenyl]propan-2-yl]phenol Chemical compound C=1C=C(C(C)(C=2C=CC(O)=CC=2)C=2C=CC(O)=CC=2)C=CC=1C(C)(C)C1=CC=C(O)C=C1 WXYSZTISEJBRHW-UHFFFAOYSA-N 0.000 description 1
- DNLWYVQYADCTEU-UHFFFAOYSA-N 4-[3-(4-hydroxyphenyl)-1-adamantyl]phenol Chemical compound C1=CC(O)=CC=C1C1(CC(C2)(C3)C=4C=CC(O)=CC=4)CC3CC2C1 DNLWYVQYADCTEU-UHFFFAOYSA-N 0.000 description 1
- ZJNKCNFBTBFNMO-UHFFFAOYSA-N 4-[3-(4-hydroxyphenyl)-5,7-dimethyl-1-adamantyl]phenol Chemical compound C1C(C)(C2)CC(C3)(C)CC1(C=1C=CC(O)=CC=1)CC23C1=CC=C(O)C=C1 ZJNKCNFBTBFNMO-UHFFFAOYSA-N 0.000 description 1
- NUDSREQIJYWLRA-UHFFFAOYSA-N 4-[9-(4-hydroxy-3-methylphenyl)fluoren-9-yl]-2-methylphenol Chemical compound C1=C(O)C(C)=CC(C2(C3=CC=CC=C3C3=CC=CC=C32)C=2C=C(C)C(O)=CC=2)=C1 NUDSREQIJYWLRA-UHFFFAOYSA-N 0.000 description 1
- FTMFBPJUFQDPJR-UHFFFAOYSA-N 4-[9-(4-methoxy-3-methylphenyl)fluoren-9-yl]-2-methylphenol Chemical compound C1=C(C)C(OC)=CC=C1C1(C=2C=C(C)C(O)=CC=2)C2=CC=CC=C2C2=CC=CC=C21 FTMFBPJUFQDPJR-UHFFFAOYSA-N 0.000 description 1
- STJJFAQLJODTGA-UHFFFAOYSA-N 4-[9-(4-methoxyphenyl)fluoren-9-yl]phenol Chemical compound C1=CC(OC)=CC=C1C1(C=2C=CC(O)=CC=2)C2=CC=CC=C2C2=CC=CC=C21 STJJFAQLJODTGA-UHFFFAOYSA-N 0.000 description 1
- VSAWBBYYMBQKIK-UHFFFAOYSA-N 4-[[3,5-bis[(3,5-ditert-butyl-4-hydroxyphenyl)methyl]-2,4,6-trimethylphenyl]methyl]-2,6-ditert-butylphenol Chemical compound CC1=C(CC=2C=C(C(O)=C(C=2)C(C)(C)C)C(C)(C)C)C(C)=C(CC=2C=C(C(O)=C(C=2)C(C)(C)C)C(C)(C)C)C(C)=C1CC1=CC(C(C)(C)C)=C(O)C(C(C)(C)C)=C1 VSAWBBYYMBQKIK-UHFFFAOYSA-N 0.000 description 1
- GKLBDKZKXSQUHM-UHFFFAOYSA-N 4-benzhydrylphenol Chemical compound C1=CC(O)=CC=C1C(C=1C=CC=CC=1)C1=CC=CC=C1 GKLBDKZKXSQUHM-UHFFFAOYSA-N 0.000 description 1
- OAHMVZYHIJQTQC-UHFFFAOYSA-N 4-cyclohexylphenol Chemical compound C1=CC(O)=CC=C1C1CCCCC1 OAHMVZYHIJQTQC-UHFFFAOYSA-N 0.000 description 1
- QOPABJOZVXZFJG-UHFFFAOYSA-N 4-diphenylphosphanylphenol Chemical compound C1=CC(O)=CC=C1P(C=1C=CC=CC=1)C1=CC=CC=C1 QOPABJOZVXZFJG-UHFFFAOYSA-N 0.000 description 1
- 229940090248 4-hydroxybenzoic acid Drugs 0.000 description 1
- 125000004203 4-hydroxyphenyl group Chemical group [H]OC1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 description 1
- UEULEVKFYSYUCZ-UHFFFAOYSA-N 4-naphthalen-1-ylphenol Chemical compound C1=CC(O)=CC=C1C1=CC=CC2=CC=CC=C12 UEULEVKFYSYUCZ-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
- YXALYBMHAYZKAP-UHFFFAOYSA-N 7-oxabicyclo[4.1.0]heptan-4-ylmethyl 7-oxabicyclo[4.1.0]heptane-4-carboxylate Chemical compound C1CC2OC2CC1C(=O)OCC1CC2OC2CC1 YXALYBMHAYZKAP-UHFFFAOYSA-N 0.000 description 1
- ADRNSOYXKABLGT-UHFFFAOYSA-N 8-methylnonyl diphenyl phosphite Chemical compound C=1C=CC=CC=1OP(OCCCCCCCC(C)C)OC1=CC=CC=C1 ADRNSOYXKABLGT-UHFFFAOYSA-N 0.000 description 1
- YWFPGFJLYRKYJZ-UHFFFAOYSA-N 9,9-bis(4-hydroxyphenyl)fluorene Chemical compound C1=CC(O)=CC=C1C1(C=2C=CC(O)=CC=2)C2=CC=CC=C2C2=CC=CC=C21 YWFPGFJLYRKYJZ-UHFFFAOYSA-N 0.000 description 1
- LEKAUMWBGMEJNW-UHFFFAOYSA-N 9,9-diphenylnonyl dihydrogen phosphite Chemical compound C=1C=CC=CC=1C(CCCCCCCCOP(O)O)C1=CC=CC=C1 LEKAUMWBGMEJNW-UHFFFAOYSA-N 0.000 description 1
- NLHHRLWOUZZQLW-UHFFFAOYSA-N Acrylonitrile Chemical group C=CC#N NLHHRLWOUZZQLW-UHFFFAOYSA-N 0.000 description 1
- 208000006096 Attention Deficit Disorder with Hyperactivity Diseases 0.000 description 1
- 208000036864 Attention deficit/hyperactivity disease Diseases 0.000 description 1
- HTVITOHKHWFJKO-UHFFFAOYSA-N Bisphenol B Chemical compound C=1C=C(O)C=CC=1C(C)(CC)C1=CC=C(O)C=C1 HTVITOHKHWFJKO-UHFFFAOYSA-N 0.000 description 1
- SDDLEVPIDBLVHC-UHFFFAOYSA-N Bisphenol Z Chemical compound C1=CC(O)=CC=C1C1(C=2C=CC(O)=CC=2)CCCCC1 SDDLEVPIDBLVHC-UHFFFAOYSA-N 0.000 description 1
- XUUFMCMZNDNJJL-UHFFFAOYSA-N C1(=CC=CC=C1)C(C1=CC=CC=C1)(P(C1=CC=CC2=CC=CC=C12)C1=CC=CC=C1)C1=CC=CC=C1 Chemical compound C1(=CC=CC=C1)C(C1=CC=CC=C1)(P(C1=CC=CC2=CC=CC=C12)C1=CC=CC=C1)C1=CC=CC=C1 XUUFMCMZNDNJJL-UHFFFAOYSA-N 0.000 description 1
- SLJFKNONPLNAPF-UHFFFAOYSA-N C=CC1CC2OC2CC1 Chemical compound C=CC1CC2OC2CC1 SLJFKNONPLNAPF-UHFFFAOYSA-N 0.000 description 1
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 description 1
- HEDRZPFGACZZDS-UHFFFAOYSA-N Chloroform Chemical compound ClC(Cl)Cl HEDRZPFGACZZDS-UHFFFAOYSA-N 0.000 description 1
- GYCKQBWUSACYIF-UHFFFAOYSA-N Ethyl salicylate Chemical compound CCOC(=O)C1=CC=CC=C1O GYCKQBWUSACYIF-UHFFFAOYSA-N 0.000 description 1
- 239000005977 Ethylene Substances 0.000 description 1
- 238000012695 Interfacial polymerization Methods 0.000 description 1
- 239000004610 Internal Lubricant Substances 0.000 description 1
- VVQNEPGJFQJSBK-UHFFFAOYSA-N Methyl methacrylate Chemical group COC(=O)C(C)=C VVQNEPGJFQJSBK-UHFFFAOYSA-N 0.000 description 1
- JLTDJTHDQAWBAV-UHFFFAOYSA-N N,N-dimethylaniline Chemical compound CN(C)C1=CC=CC=C1 JLTDJTHDQAWBAV-UHFFFAOYSA-N 0.000 description 1
- SVYKKECYCPFKGB-UHFFFAOYSA-N N,N-dimethylcyclohexylamine Chemical compound CN(C)C1CCCCC1 SVYKKECYCPFKGB-UHFFFAOYSA-N 0.000 description 1
- 239000004698 Polyethylene Substances 0.000 description 1
- 239000002202 Polyethylene glycol Substances 0.000 description 1
- XBDQKXXYIPTUBI-UHFFFAOYSA-M Propionate Chemical compound CCC([O-])=O XBDQKXXYIPTUBI-UHFFFAOYSA-M 0.000 description 1
- 229920000297 Rayon Polymers 0.000 description 1
- 229920002125 Sokalan® Polymers 0.000 description 1
- 229910000831 Steel Inorganic materials 0.000 description 1
- CGRTZESQZZGAAU-UHFFFAOYSA-N [2-[3-[1-[3-(3-tert-butyl-4-hydroxy-5-methylphenyl)propanoyloxy]-2-methylpropan-2-yl]-2,4,8,10-tetraoxaspiro[5.5]undecan-9-yl]-2-methylpropyl] 3-(3-tert-butyl-4-hydroxy-5-methylphenyl)propanoate Chemical compound CC(C)(C)C1=C(O)C(C)=CC(CCC(=O)OCC(C)(C)C2OCC3(CO2)COC(OC3)C(C)(C)COC(=O)CCC=2C=C(C(O)=C(C)C=2)C(C)(C)C)=C1 CGRTZESQZZGAAU-UHFFFAOYSA-N 0.000 description 1
- BGYHLZZASRKEJE-UHFFFAOYSA-N [3-[3-(3,5-ditert-butyl-4-hydroxyphenyl)propanoyloxy]-2,2-bis[3-(3,5-ditert-butyl-4-hydroxyphenyl)propanoyloxymethyl]propyl] 3-(3,5-ditert-butyl-4-hydroxyphenyl)propanoate Chemical compound CC(C)(C)C1=C(O)C(C(C)(C)C)=CC(CCC(=O)OCC(COC(=O)CCC=2C=C(C(O)=C(C=2)C(C)(C)C)C(C)(C)C)(COC(=O)CCC=2C=C(C(O)=C(C=2)C(C)(C)C)C(C)(C)C)COC(=O)CCC=2C=C(C(O)=C(C=2)C(C)(C)C)C(C)(C)C)=C1 BGYHLZZASRKEJE-UHFFFAOYSA-N 0.000 description 1
- 239000006096 absorbing agent Substances 0.000 description 1
- 239000002253 acid Substances 0.000 description 1
- XECAHXYUAAWDEL-UHFFFAOYSA-N acrylonitrile butadiene styrene Chemical compound C=CC=C.C=CC#N.C=CC1=CC=CC=C1 XECAHXYUAAWDEL-UHFFFAOYSA-N 0.000 description 1
- 239000004676 acrylonitrile butadiene styrene Substances 0.000 description 1
- 229920000122 acrylonitrile butadiene styrene Polymers 0.000 description 1
- 230000000996 additive effect Effects 0.000 description 1
- 125000001931 aliphatic group Chemical group 0.000 description 1
- 150000005215 alkyl ethers Chemical class 0.000 description 1
- 239000002216 antistatic agent Substances 0.000 description 1
- 239000007864 aqueous solution Substances 0.000 description 1
- 239000007869 azo polymerization initiator Substances 0.000 description 1
- 230000008901 benefit Effects 0.000 description 1
- RWCCWEUUXYIKHB-UHFFFAOYSA-N benzophenone Chemical compound C=1C=CC=CC=1C(=O)C1=CC=CC=C1 RWCCWEUUXYIKHB-UHFFFAOYSA-N 0.000 description 1
- 239000012965 benzophenone Substances 0.000 description 1
- QRUDEWIWKLJBPS-UHFFFAOYSA-N benzotriazole Chemical compound C1=CC=C2N[N][N]C2=C1 QRUDEWIWKLJBPS-UHFFFAOYSA-N 0.000 description 1
- 239000012964 benzotriazole Substances 0.000 description 1
- VJGNLOIQCWLBJR-UHFFFAOYSA-M benzyl(tributyl)azanium;chloride Chemical compound [Cl-].CCCC[N+](CCCC)(CCCC)CC1=CC=CC=C1 VJGNLOIQCWLBJR-UHFFFAOYSA-M 0.000 description 1
- HTZCNXWZYVXIMZ-UHFFFAOYSA-M benzyl(triethyl)azanium;chloride Chemical compound [Cl-].CC[N+](CC)(CC)CC1=CC=CC=C1 HTZCNXWZYVXIMZ-UHFFFAOYSA-M 0.000 description 1
- KXHPPCXNWTUNSB-UHFFFAOYSA-M benzyl(trimethyl)azanium;chloride Chemical compound [Cl-].C[N+](C)(C)CC1=CC=CC=C1 KXHPPCXNWTUNSB-UHFFFAOYSA-M 0.000 description 1
- 235000010290 biphenyl Nutrition 0.000 description 1
- 239000004305 biphenyl Substances 0.000 description 1
- UBXYXCRCOKCZIT-UHFFFAOYSA-N biphenyl-3-ol Chemical compound OC1=CC=CC(C=2C=CC=CC=2)=C1 UBXYXCRCOKCZIT-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
- SXDBWCPKPHAZSM-UHFFFAOYSA-M bromate Inorganic materials [O-]Br(=O)=O SXDBWCPKPHAZSM-UHFFFAOYSA-M 0.000 description 1
- SXDBWCPKPHAZSM-UHFFFAOYSA-N bromic acid Chemical compound OBr(=O)=O SXDBWCPKPHAZSM-UHFFFAOYSA-N 0.000 description 1
- 238000012662 bulk polymerization Methods 0.000 description 1
- 239000001273 butane Substances 0.000 description 1
- 229910052799 carbon Inorganic materials 0.000 description 1
- 238000006243 chemical reaction Methods 0.000 description 1
- 150000008280 chlorinated hydrocarbons Chemical class 0.000 description 1
- 229960001701 chloroform Drugs 0.000 description 1
- 239000003086 colorant Substances 0.000 description 1
- 125000004122 cyclic group Chemical group 0.000 description 1
- MIHINWMALJZIBX-UHFFFAOYSA-N cyclohexa-2,4-dien-1-ol Chemical class OC1CC=CC=C1 MIHINWMALJZIBX-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
- 125000004956 cyclohexylene group Chemical group 0.000 description 1
- 125000001511 cyclopentyl group Chemical group [H]C1([H])C([H])([H])C([H])([H])C([H])(*)C1([H])[H] 0.000 description 1
- 125000004979 cyclopentylene group Chemical group 0.000 description 1
- 230000007850 degeneration Effects 0.000 description 1
- UZEFVQBWJSFOFE-UHFFFAOYSA-N dibutyl hydrogen phosphite Chemical compound CCCCOP(O)OCCCC UZEFVQBWJSFOFE-UHFFFAOYSA-N 0.000 description 1
- GCDUSCPJMVWSBD-UHFFFAOYSA-N diphenylphosphanylmethyl acetate Chemical compound C=1C=CC=CC=1P(COC(=O)C)C1=CC=CC=C1 GCDUSCPJMVWSBD-UHFFFAOYSA-N 0.000 description 1
- 229920001971 elastomer Polymers 0.000 description 1
- 239000000806 elastomer Substances 0.000 description 1
- 238000005516 engineering process Methods 0.000 description 1
- 150000002148 esters Chemical class 0.000 description 1
- 125000001033 ether group Chemical group 0.000 description 1
- 125000000816 ethylene group Chemical group [H]C([H])([*:1])C([H])([H])[*:2] 0.000 description 1
- 125000000219 ethylidene group Chemical group [H]C(=[*])C([H])([H])[H] 0.000 description 1
- 238000005469 granulation Methods 0.000 description 1
- 230000003179 granulation Effects 0.000 description 1
- 125000004836 hexamethylene group Chemical group [H]C([H])([*:2])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])[*:1] 0.000 description 1
- 229920001519 homopolymer Polymers 0.000 description 1
- 230000007062 hydrolysis Effects 0.000 description 1
- 238000006460 hydrolysis reaction Methods 0.000 description 1
- 125000002887 hydroxy group Chemical group [H]O* 0.000 description 1
- 230000006872 improvement Effects 0.000 description 1
- 239000012442 inert solvent Substances 0.000 description 1
- 125000000959 isobutyl group Chemical group [H]C([H])([H])C([H])(C([H])([H])[H])C([H])([H])* 0.000 description 1
- 125000000654 isopropylidene group Chemical group C(C)(C)=* 0.000 description 1
- 239000004611 light stabiliser Substances 0.000 description 1
- 238000000691 measurement method Methods 0.000 description 1
- OSWPMRLSEDHDFF-UHFFFAOYSA-N methyl salicylate Chemical compound COC(=O)C1=CC=CC=C1O OSWPMRLSEDHDFF-UHFFFAOYSA-N 0.000 description 1
- 125000001570 methylene group Chemical group [H]C([H])([*:1])[*:2] 0.000 description 1
- 125000000325 methylidene group Chemical group [H]C([H])=* 0.000 description 1
- XKBGEWXEAPTVCK-UHFFFAOYSA-M methyltrioctylammonium chloride Chemical compound [Cl-].CCCCCCCC[N+](C)(CCCCCCCC)CCCCCCCC XKBGEWXEAPTVCK-UHFFFAOYSA-M 0.000 description 1
- 239000003607 modifier Substances 0.000 description 1
- 239000000178 monomer Substances 0.000 description 1
- IJDNQMDRQITEOD-UHFFFAOYSA-N n-butane Chemical compound CCCC IJDNQMDRQITEOD-UHFFFAOYSA-N 0.000 description 1
- 125000004108 n-butyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])C([H])([H])* 0.000 description 1
- OFBQJSOFQDEBGM-UHFFFAOYSA-N n-pentane Natural products CCCCC OFBQJSOFQDEBGM-UHFFFAOYSA-N 0.000 description 1
- JFNLZVQOOSMTJK-KNVOCYPGSA-N norbornene Chemical compound C1[C@@H]2CC[C@H]1C=C2 JFNLZVQOOSMTJK-KNVOCYPGSA-N 0.000 description 1
- SSDSCDGVMJFTEQ-UHFFFAOYSA-N octadecyl 3-(3,5-ditert-butyl-4-hydroxyphenyl)propanoate Chemical compound CCCCCCCCCCCCCCCCCCOC(=O)CCC1=CC(C(C)(C)C)=C(O)C(C(C)(C)C)=C1 SSDSCDGVMJFTEQ-UHFFFAOYSA-N 0.000 description 1
- 150000002905 orthoesters Chemical class 0.000 description 1
- 235000010292 orthophenyl phenol Nutrition 0.000 description 1
- ACMVLJBSYFHILY-UHFFFAOYSA-N oxo-di(tridecoxy)phosphanium Chemical compound CCCCCCCCCCCCCO[P+](=O)OCCCCCCCCCCCCC ACMVLJBSYFHILY-UHFFFAOYSA-N 0.000 description 1
- 125000004430 oxygen atom Chemical group O* 0.000 description 1
- NFHFRUOZVGFOOS-UHFFFAOYSA-N palladium;triphenylphosphane Chemical compound [Pd].C1=CC=CC=C1P(C=1C=CC=CC=1)C1=CC=CC=C1.C1=CC=CC=C1P(C=1C=CC=CC=1)C1=CC=CC=C1.C1=CC=CC=C1P(C=1C=CC=CC=1)C1=CC=CC=C1.C1=CC=CC=C1P(C=1C=CC=CC=1)C1=CC=CC=C1 NFHFRUOZVGFOOS-UHFFFAOYSA-N 0.000 description 1
- 239000012188 paraffin wax Substances 0.000 description 1
- BNIXVQGCZULYKV-UHFFFAOYSA-N pentachloroethane Chemical compound ClC(Cl)C(Cl)(Cl)Cl BNIXVQGCZULYKV-UHFFFAOYSA-N 0.000 description 1
- 230000035699 permeability Effects 0.000 description 1
- 150000002978 peroxides Chemical class 0.000 description 1
- 238000005191 phase separation Methods 0.000 description 1
- 239000003444 phase transfer catalyst Substances 0.000 description 1
- ZUOUZKKEUPVFJK-UHFFFAOYSA-N phenylbenzene Natural products C1=CC=CC=C1C1=CC=CC=C1 ZUOUZKKEUPVFJK-UHFFFAOYSA-N 0.000 description 1
- 229960001553 phloroglucinol Drugs 0.000 description 1
- QCDYQQDYXPDABM-UHFFFAOYSA-N phloroglucinol Chemical group OC1=CC(O)=CC(O)=C1 QCDYQQDYXPDABM-UHFFFAOYSA-N 0.000 description 1
- 239000004584 polyacrylic acid Substances 0.000 description 1
- 229920002239 polyacrylonitrile Polymers 0.000 description 1
- 229920000573 polyethylene Polymers 0.000 description 1
- 229920001223 polyethylene glycol Polymers 0.000 description 1
- 229920000642 polymer Polymers 0.000 description 1
- 238000006116 polymerization reaction Methods 0.000 description 1
- 229920001451 polypropylene glycol Polymers 0.000 description 1
- 125000004805 propylene group Chemical group [H]C([H])([H])C([H])([*:1])C([H])([H])[*:2] 0.000 description 1
- 238000000746 purification Methods 0.000 description 1
- UMJSCPRVCHMLSP-UHFFFAOYSA-N pyridine Natural products COC1=CC=CN=C1 UMJSCPRVCHMLSP-UHFFFAOYSA-N 0.000 description 1
- 230000009257 reactivity Effects 0.000 description 1
- 150000003839 salts Chemical class 0.000 description 1
- 229920002545 silicone oil Polymers 0.000 description 1
- 239000004332 silver Substances 0.000 description 1
- 229910052709 silver Inorganic materials 0.000 description 1
- 239000011734 sodium Substances 0.000 description 1
- 229910052708 sodium Inorganic materials 0.000 description 1
- 125000001424 substituent group Chemical group 0.000 description 1
- 150000003462 sulfoxides Chemical class 0.000 description 1
- JRMUNVKIHCOMHV-UHFFFAOYSA-M tetrabutylammonium bromide Chemical compound [Br-].CCCC[N+](CCCC)(CCCC)CCCC JRMUNVKIHCOMHV-UHFFFAOYSA-M 0.000 description 1
- RKHXQBLJXBGEKF-UHFFFAOYSA-M tetrabutylphosphanium;bromide Chemical compound [Br-].CCCC[P+](CCCC)(CCCC)CCCC RKHXQBLJXBGEKF-UHFFFAOYSA-M 0.000 description 1
- IBWGNZVCJVLSHB-UHFFFAOYSA-M tetrabutylphosphanium;chloride Chemical compound [Cl-].CCCC[P+](CCCC)(CCCC)CCCC IBWGNZVCJVLSHB-UHFFFAOYSA-M 0.000 description 1
- 125000000383 tetramethylene group Chemical group [H]C([H])([*:1])C([H])([H])C([H])([H])C([H])([H])[*:2] 0.000 description 1
- IMFACGCPASFAPR-UHFFFAOYSA-N tributylamine Chemical compound CCCCN(CCCC)CCCC IMFACGCPASFAPR-UHFFFAOYSA-N 0.000 description 1
- DMEUUKUNSVFYAA-UHFFFAOYSA-N trinaphthalen-1-ylphosphane Chemical compound C1=CC=C2C(P(C=3C4=CC=CC=C4C=CC=3)C=3C4=CC=CC=C4C=CC=3)=CC=CC2=C1 DMEUUKUNSVFYAA-UHFFFAOYSA-N 0.000 description 1
- LENZDBCJOHFCAS-UHFFFAOYSA-N tris Chemical compound OCC(N)(CO)CO LENZDBCJOHFCAS-UHFFFAOYSA-N 0.000 description 1
- JNJGSDYMEKOBPD-UHFFFAOYSA-N tris(4-nonylphenyl)phosphane Chemical compound C1=CC(CCCCCCCCC)=CC=C1P(C=1C=CC(CCCCCCCCC)=CC=1)C1=CC=C(CCCCCCCCC)C=C1 JNJGSDYMEKOBPD-UHFFFAOYSA-N 0.000 description 1
- 229940088594 vitamin Drugs 0.000 description 1
- 229930003231 vitamin Natural products 0.000 description 1
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 1
- 239000001993 wax Substances 0.000 description 1
- 238000004383 yellowing Methods 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08G—MACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
- C08G64/00—Macromolecular compounds obtained by reactions forming a carbonic ester link in the main chain of the macromolecule
- C08G64/04—Aromatic polycarbonates
- C08G64/06—Aromatic polycarbonates not containing aliphatic unsaturation
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B29—WORKING OF PLASTICS; WORKING OF SUBSTANCES IN A PLASTIC STATE IN GENERAL
- B29B—PREPARATION OR PRETREATMENT OF THE MATERIAL TO BE SHAPED; MAKING GRANULES OR PREFORMS; RECOVERY OF PLASTICS OR OTHER CONSTITUENTS OF WASTE MATERIAL CONTAINING PLASTICS
- B29B9/00—Making granules
- B29B9/12—Making granules characterised by structure or composition
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B29—WORKING OF PLASTICS; WORKING OF SUBSTANCES IN A PLASTIC STATE IN GENERAL
- B29C—SHAPING OR JOINING OF PLASTICS; SHAPING OF MATERIAL IN A PLASTIC STATE, NOT OTHERWISE PROVIDED FOR; AFTER-TREATMENT OF THE SHAPED PRODUCTS, e.g. REPAIRING
- B29C48/00—Extrusion moulding, i.e. expressing the moulding material through a die or nozzle which imparts the desired form; Apparatus therefor
- B29C48/03—Extrusion moulding, i.e. expressing the moulding material through a die or nozzle which imparts the desired form; Apparatus therefor characterised by the shape of the extruded material at extrusion
- B29C48/04—Particle-shaped
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08K—Use of inorganic or non-macromolecular organic substances as compounding ingredients
- C08K5/00—Use of organic ingredients
- C08K5/49—Phosphorus-containing compounds
- C08K5/51—Phosphorus bound to oxygen
- C08K5/52—Phosphorus bound to oxygen only
- C08K5/524—Esters of phosphorous acids, e.g. of H3PO3
-
- 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
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08L—COMPOSITIONS OF MACROMOLECULAR COMPOUNDS
- C08L83/00—Compositions of macromolecular compounds obtained by reactions forming in the main chain of the macromolecule a linkage containing silicon with or without sulfur, nitrogen, oxygen or carbon only; Compositions of derivatives of such polymers
- C08L83/04—Polysiloxanes
-
- F—MECHANICAL ENGINEERING; LIGHTING; HEATING; WEAPONS; BLASTING
- F21—LIGHTING
- F21S—NON-PORTABLE LIGHTING DEVICES; SYSTEMS THEREOF; VEHICLE LIGHTING DEVICES SPECIALLY ADAPTED FOR VEHICLE EXTERIORS
- F21S2/00—Systems of lighting devices, not provided for in main groups F21S4/00 - F21S10/00 or F21S19/00, e.g. of modular construction
-
- G—PHYSICS
- G02—OPTICS
- G02B—OPTICAL ELEMENTS, SYSTEMS OR APPARATUS
- G02B1/00—Optical elements characterised by the material of which they are made; Optical coatings for optical elements
- G02B1/04—Optical elements characterised by the material of which they are made; Optical coatings for optical elements made of organic materials, e.g. plastics
- G02B1/045—Light guides
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B29—WORKING OF PLASTICS; WORKING OF SUBSTANCES IN A PLASTIC STATE IN GENERAL
- B29B—PREPARATION OR PRETREATMENT OF THE MATERIAL TO BE SHAPED; MAKING GRANULES OR PREFORMS; RECOVERY OF PLASTICS OR OTHER CONSTITUENTS OF WASTE MATERIAL CONTAINING PLASTICS
- B29B9/00—Making granules
- B29B9/02—Making granules by dividing preformed material
- B29B9/06—Making granules by dividing preformed material in the form of filamentary material, e.g. combined with extrusion
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08K—Use of inorganic or non-macromolecular organic substances as compounding ingredients
- C08K5/00—Use of organic ingredients
- C08K5/04—Oxygen-containing compounds
- C08K5/10—Esters; Ether-esters
- C08K5/101—Esters; Ether-esters of monocarboxylic acids
- C08K5/103—Esters; Ether-esters of monocarboxylic acids with polyalcohols
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08K—Use of inorganic or non-macromolecular organic substances as compounding ingredients
- C08K5/00—Use of organic ingredients
- C08K5/49—Phosphorus-containing compounds
- C08K5/51—Phosphorus bound to oxygen
- C08K5/52—Phosphorus bound to oxygen only
- C08K5/527—Cyclic esters
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08L—COMPOSITIONS OF MACROMOLECULAR COMPOUNDS
- C08L2205/00—Polymer mixtures characterised by other features
- C08L2205/02—Polymer mixtures characterised by other features containing two or more polymers of the same C08L -group
- C08L2205/025—Polymer mixtures characterised by other features containing two or more polymers of the same C08L -group containing two or more polymers of the same hierarchy C08L, and differing only in parameters such as density, comonomer content, molecular weight, structure
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08L—COMPOSITIONS OF MACROMOLECULAR COMPOUNDS
- C08L2205/00—Polymer mixtures characterised by other features
- C08L2205/03—Polymer mixtures characterised by other features containing three or more polymers in a blend
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08L—COMPOSITIONS OF MACROMOLECULAR COMPOUNDS
- C08L2205/00—Polymer mixtures characterised by other features
- C08L2205/03—Polymer mixtures characterised by other features containing three or more polymers in a blend
- C08L2205/035—Polymer mixtures characterised by other features containing three or more polymers in a blend containing four or more polymers in a blend
Landscapes
- Chemical & Material Sciences (AREA)
- Health & Medical Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Medicinal Chemistry (AREA)
- Polymers & Plastics (AREA)
- Organic Chemistry (AREA)
- Engineering & Computer Science (AREA)
- Mechanical Engineering (AREA)
- Physics & Mathematics (AREA)
- General Physics & Mathematics (AREA)
- Optics & Photonics (AREA)
- General Engineering & Computer Science (AREA)
- Compositions Of Macromolecular Compounds (AREA)
- Planar Illumination Modules (AREA)
- Processing And Handling Of Plastics And Other Materials For Molding In General (AREA)
- Polyesters Or Polycarbonates (AREA)
Applications Claiming Priority (3)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP2011290051A JP5879124B2 (ja) | 2011-12-28 | 2011-12-28 | ポリカーボネート樹脂組成物ペレットの製造方法 |
| JPJP-P-2011-290051 | 2011-12-28 | ||
| PCT/JP2012/083966 WO2013100090A1 (ja) | 2011-12-28 | 2012-12-27 | ポリカーボネート樹脂組成物ペレット及びその製造方法 |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| KR20140115305A KR20140115305A (ko) | 2014-09-30 |
| KR101923256B1 true KR101923256B1 (ko) | 2018-11-28 |
Family
ID=48697569
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| KR1020147017611A Active KR101923256B1 (ko) | 2011-12-28 | 2012-12-27 | 폴리카보네이트 수지 조성물 펠릿 및 그 제조 방법 |
Country Status (7)
| Country | Link |
|---|---|
| US (1) | US9593202B2 (https=) |
| EP (1) | EP2799200B1 (https=) |
| JP (1) | JP5879124B2 (https=) |
| KR (1) | KR101923256B1 (https=) |
| CN (1) | CN104023928B (https=) |
| TW (1) | TWI582162B (https=) |
| WO (1) | WO2013100090A1 (https=) |
Families Citing this family (50)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| KR102121093B1 (ko) * | 2013-07-26 | 2020-06-09 | 미쓰비시 엔지니어링-플라스틱스 코포레이션 | 박육 광학 부품용 폴리카르보네이트 수지 조성물 및 박육 광학 부품 |
| WO2015011994A1 (ja) * | 2013-07-26 | 2015-01-29 | 三菱エンジニアリングプラスチックス株式会社 | 薄肉光学部品用ポリカーボネート樹脂組成物および薄肉光学部品 |
| JP5699240B1 (ja) * | 2014-03-06 | 2015-04-08 | 三菱エンジニアリングプラスチックス株式会社 | 薄肉光学部品用ポリカーボネート樹脂組成物および薄肉光学部品 |
| JP5699188B2 (ja) * | 2013-07-26 | 2015-04-08 | 三菱エンジニアリングプラスチックス株式会社 | 薄肉光学部品用ポリカーボネート樹脂組成物および薄肉光学部品 |
| US9303121B2 (en) * | 2013-08-29 | 2016-04-05 | Lg Chem, Ltd. | Terminally modified polyoxyalkylene glycol and polycarbonate resin composition having improved optical characteristics comprising the same |
| JP6828954B2 (ja) * | 2013-11-11 | 2021-02-10 | 出光興産株式会社 | ポリカーボネート樹脂成形材料 |
| JP7106809B2 (ja) | 2013-11-11 | 2022-07-27 | 出光興産株式会社 | 芳香族ポリカーボネート樹脂成形体 |
| JP6408760B2 (ja) | 2013-11-11 | 2018-10-17 | 出光興産株式会社 | ポリカーボネート樹脂組成物 |
| ES2689690T3 (es) * | 2013-12-10 | 2018-11-15 | Sumika Polycarbonate Limited | Composición de resina de policarbonato y artículo óptico moldeado |
| WO2015129638A1 (ja) * | 2014-02-28 | 2015-09-03 | 出光興産株式会社 | ポリカーボネート樹脂及びポリカーボネート樹脂組成物 |
| WO2015129639A1 (ja) * | 2014-02-28 | 2015-09-03 | 出光興産株式会社 | ポリカーボネート樹脂及びポリカーボネート樹脂組成物 |
| JP6303707B2 (ja) * | 2014-03-28 | 2018-04-04 | 三菱エンジニアリングプラスチックス株式会社 | 芳香族ポリカーボネート樹脂組成物及びその成形品 |
| JP6575979B2 (ja) * | 2014-07-09 | 2019-09-18 | 出光興産株式会社 | 芳香族ポリカーボネート樹脂組成物及びその成形品 |
| JP6770434B2 (ja) * | 2014-10-17 | 2020-10-14 | 出光興産株式会社 | ポリカーボネート樹脂組成物 |
| JP6396792B2 (ja) * | 2014-12-25 | 2018-09-26 | 三菱エンジニアリングプラスチックス株式会社 | 導光部材用ポリカーボネート樹脂組成物及び導光部材 |
| JP6101745B2 (ja) | 2015-01-07 | 2017-03-22 | 三菱エンジニアリングプラスチックス株式会社 | 薄肉光学部品用ポリカーボネート樹脂組成物および薄肉光学部品 |
| JP5991420B2 (ja) * | 2015-02-03 | 2016-09-14 | 三菱エンジニアリングプラスチックス株式会社 | 芳香族ポリカーボネート樹脂組成物及びその成形品 |
| EP3255105B1 (en) * | 2015-02-03 | 2022-06-01 | Mitsubishi Engineering-Plastics Corporation | Aromatic polycarbonate resin composition and molded article of same |
| US20170349729A1 (en) * | 2015-02-03 | 2017-12-07 | c/o Mitsubishi Engineering-Plastics Corporation | Aromatic polycarbonate resin composition and molded article thereof |
| JP6472321B2 (ja) * | 2015-05-18 | 2019-02-20 | 住化ポリカーボネート株式会社 | ポリカーボネート樹脂組成物及びそれからなる成形品 |
| US11034834B2 (en) | 2015-05-29 | 2021-06-15 | Idemitsu Kosan Co., Ltd. | Polycarbonate resin composition and molded article of same |
| JP2017002295A (ja) * | 2015-06-09 | 2017-01-05 | 住化スタイロンポリカーボネート株式会社 | 光学部品用ポリカーボネート樹脂組成物及びそれからなる成形品 |
| JP5991447B1 (ja) * | 2015-06-11 | 2016-09-14 | 三菱エンジニアリングプラスチックス株式会社 | 芳香族ポリカーボネート樹脂組成物及びその成形品 |
| KR101956832B1 (ko) | 2015-06-12 | 2019-03-12 | 주식회사 엘지화학 | 폴리카보네이트 수지 조성물 및 이로 이루어진 광학 성형품 |
| US20180371235A1 (en) * | 2015-11-20 | 2018-12-27 | Idemitsu Kosan Co., Ltd. | Polycarbonate resin composition and molded product thereof |
| JP6156561B2 (ja) | 2015-11-27 | 2017-07-05 | 三菱エンジニアリングプラスチックス株式会社 | 芳香族ポリカーボネート樹脂組成物及びその成形品 |
| KR102562544B1 (ko) | 2015-12-11 | 2023-08-03 | 미쯔비시 케미컬 주식회사 | 박육 광학 부품용 폴리카르보네이트 수지 조성물 및 박육 광학 부품의 제조 방법 |
| US10385163B2 (en) * | 2016-02-18 | 2019-08-20 | Lg Chem, Ltd. | Polycarbonate resin composition and optical molded article using the same |
| JP6642295B2 (ja) * | 2016-06-20 | 2020-02-05 | 出光興産株式会社 | ポリカーボネート樹脂成形材料 |
| JP6898192B2 (ja) * | 2016-09-30 | 2021-07-07 | マツダ株式会社 | 自動車用内外装部材 |
| US20180094133A1 (en) * | 2016-09-30 | 2018-04-05 | Mazda Motor Corporation | Interior/exterior automotive trim component |
| CN113683877A (zh) * | 2016-11-28 | 2021-11-23 | 三菱工程塑料株式会社 | 聚碳酸酯树脂组合物 |
| JP6960799B2 (ja) * | 2016-11-28 | 2021-11-05 | 三菱エンジニアリングプラスチックス株式会社 | ポリカーボネート樹脂組成物 |
| JP2019019301A (ja) * | 2016-11-28 | 2019-02-07 | 三菱エンジニアリングプラスチックス株式会社 | ポリカーボネート樹脂組成物 |
| WO2018096758A1 (ja) * | 2016-11-28 | 2018-05-31 | 三菱エンジニアリングプラスチックス株式会社 | ポリカーボネート樹脂組成物 |
| JP6822126B2 (ja) * | 2016-12-20 | 2021-01-27 | 三菱エンジニアリングプラスチックス株式会社 | 芳香族ポリカーボネート樹脂組成物及びその成形品 |
| WO2018181947A1 (ja) * | 2017-03-30 | 2018-10-04 | 出光興産株式会社 | ポリカーボネート樹脂組成物及び成形体 |
| WO2018230662A1 (ja) | 2017-06-14 | 2018-12-20 | 三菱ケミカル株式会社 | 芳香族ポリカーボネート樹脂、及びその製造方法、並びに芳香族ジヒドロキシ化合物 |
| JP6480068B1 (ja) * | 2018-01-26 | 2019-03-06 | 住化ポリカーボネート株式会社 | 芳香族ポリカーボネート樹脂組成物および光学用成形品 |
| CN111630108B (zh) * | 2018-01-26 | 2022-12-27 | 住化Pc有限公司 | 芳香族聚碳酸酯树脂组合物和光学用成型品 |
| JP7155593B2 (ja) * | 2018-04-27 | 2022-10-19 | 三菱エンジニアリングプラスチックス株式会社 | 自動車用照明装置の導光部材用ポリカーボネート樹脂組成物ペレットの製造方法及び自動車用照明装置の導光部材の製造方法 |
| JP6526871B2 (ja) * | 2018-05-01 | 2019-06-05 | 三菱エンジニアリングプラスチックス株式会社 | 薄肉光学部品用ポリカーボネート樹脂組成物および薄肉光学部品 |
| EP3575362A1 (de) | 2018-05-29 | 2019-12-04 | Covestro Deutschland AG | Abdeckungen für led-lichtquellen |
| JP6674526B1 (ja) * | 2018-12-19 | 2020-04-01 | 住化ポリカーボネート株式会社 | 芳香族ポリカーボネート樹脂組成物および光学用成形品 |
| JP6629473B1 (ja) * | 2019-02-27 | 2020-01-15 | 住化ポリカーボネート株式会社 | 芳香族ポリカーボネート樹脂組成物および光学用成形品 |
| JP7214614B2 (ja) * | 2019-12-04 | 2023-01-30 | 住化ポリカーボネート株式会社 | 芳香族ポリカーボネート樹脂組成物および光学用成形品 |
| JP7239512B2 (ja) * | 2020-03-06 | 2023-03-14 | 住化ポリカーボネート株式会社 | 芳香族ポリカーボネート樹脂組成物および光学用成形品 |
| JP2020100849A (ja) * | 2020-03-27 | 2020-07-02 | 住化ポリカーボネート株式会社 | 芳香族ポリカーボネート樹脂組成物および光学用成形品 |
| JP7739723B2 (ja) * | 2021-02-26 | 2025-09-17 | 三菱ケミカル株式会社 | 活性エネルギー線硬化型樹脂組成物及びコーティング剤 |
| JP7553748B2 (ja) * | 2022-07-13 | 2024-09-18 | 住化ポリカーボネート株式会社 | 芳香族ポリカーボネート樹脂組成物および光拡散性成形品 |
Citations (4)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JP2002060609A (ja) | 2000-08-18 | 2002-02-26 | Idemitsu Petrochem Co Ltd | 芳香族ポリカーボネート樹脂組成物および成形品 |
| JP2005096421A (ja) | 2003-09-02 | 2005-04-14 | Mitsubishi Engineering Plastics Corp | 導光板用芳香族ポリカーボネート樹脂ペレット、導光板、導光板の製造方法および面光源体 |
| JP2007204737A (ja) * | 2006-01-06 | 2007-08-16 | Mitsubishi Engineering Plastics Corp | 導光板用芳香族ポリカーボネート樹脂組成物および導光板 |
| JP2008202026A (ja) | 2007-01-24 | 2008-09-04 | Mitsubishi Chemicals Corp | 芳香族ポリカーボネートの製造方法 |
Family Cites Families (28)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| DE2426714C3 (de) * | 1974-06-01 | 1978-12-14 | Dynamit Nobel Ag, 5210 Toisdorf | Verfahren zum Zuführen der Ausgangsmaterialien in eine Schneckenpresse zum Herstellen einer Folienbahn |
| DE3331903A1 (de) | 1983-09-03 | 1985-03-21 | Basf Farben + Fasern Ag, 2000 Hamburg | Wasserdispergierbare bindemittel fuer kationische elektrotauchlacke und verfahren zu ihrer herstellung |
| US4663399A (en) | 1985-08-22 | 1987-05-05 | General Electric Company | Polycarbonate-polyether block copolymers, polymer blends containing same and intermediates for the production thereof |
| ES2068911T3 (es) | 1988-07-28 | 1995-05-01 | Ciba Geigy Ag | Combinaciones de flexibilizadores para resinas epoxi. |
| US5180786A (en) * | 1988-11-09 | 1993-01-19 | Hitachi Chemical Company, Ltd. | Impact modifier, thermoplastic resin composition using the same and molded article obtained therefrom |
| JPH02180954A (ja) * | 1988-12-30 | 1990-07-13 | Kuraray Co Ltd | 光学的特性の優れた樹脂組成物およびその製法 |
| JP2844697B2 (ja) * | 1989-07-25 | 1999-01-06 | 三菱瓦斯化学株式会社 | 低ダストポリカーボネート成形品の製造法 |
| DE69716789T2 (de) * | 1996-01-26 | 2003-07-03 | Teijin Chemicals Ltd., Tokio/Tokyo | Brillenglas |
| JP4104707B2 (ja) | 1997-11-27 | 2008-06-18 | 出光興産株式会社 | ポリカーボネート樹脂組成物及び導光板 |
| TWI296635B (https=) | 2000-09-08 | 2008-05-11 | Asahi Kasei Chemicals Corp | |
| JP4744034B2 (ja) * | 2000-09-08 | 2011-08-10 | 旭化成ケミカルズ株式会社 | 難燃性ポリカーボネート樹脂組成物の製造方法 |
| JP2002173465A (ja) | 2000-09-29 | 2002-06-21 | Sanyo Chem Ind Ltd | 脱水縮合物の製造方法 |
| US20050049368A1 (en) | 2003-09-02 | 2005-03-03 | Mitsubishi Engineering-Plastic Corporation | Aromatic polycarbonate resin pellets for light guide plate, light guide plate, method for producing light guide plate and surface light source unit using the same |
| JP4478428B2 (ja) | 2003-10-07 | 2010-06-09 | 出光興産株式会社 | ポリカーボネート系樹脂組成物及び光学部品 |
| JP4792202B2 (ja) | 2004-03-03 | 2011-10-12 | 出光興産株式会社 | ポリカーボネート共重合体、ポリカーボネート共重合体組成物及びそれらからなる光学成形品 |
| JP5063873B2 (ja) * | 2005-07-05 | 2012-10-31 | 出光興産株式会社 | 光拡散性ポリカーボネート系樹脂組成物、および同樹脂組成物を用いた光拡散板 |
| JP5073939B2 (ja) * | 2005-11-08 | 2012-11-14 | 三菱エンジニアリングプラスチックス株式会社 | 導光板 |
| WO2007077874A1 (ja) | 2006-01-06 | 2007-07-12 | Mitsubishi Engineering-Plastics Corporation | 導光板用芳香族ポリカーボネート樹脂組成物および導光板 |
| WO2007129559A1 (ja) | 2006-05-01 | 2007-11-15 | Idemitsu Kosan Co., Ltd. | ポリカーボネート系樹脂組成物、それを用いた光学成形体及び照明ユニット |
| JP5064720B2 (ja) * | 2006-05-11 | 2012-10-31 | 出光興産株式会社 | ポリカーボネート系樹脂組成物、それを用いた光学成形体及び照明ユニット |
| JP5047543B2 (ja) * | 2006-06-19 | 2012-10-10 | 出光興産株式会社 | ポリカーボネート系光拡散性樹脂組成物および光拡散板 |
| JP5654727B2 (ja) * | 2008-06-17 | 2015-01-14 | 出光興産株式会社 | ポリカーボネート共重合体およびその製造方法、樹脂組成物ならびに成形品 |
| JP5593040B2 (ja) * | 2009-05-29 | 2014-09-17 | 出光興産株式会社 | ポリカーボネート樹脂組成物、および前記樹脂組成物からなる成形品 |
| EP2455798B1 (en) * | 2009-07-15 | 2015-07-08 | Menicon Co., Ltd. | Process for production of polycarbonate material having excellent solubility and affinity, and material for contact lens comprising the same |
| DE102009043513A1 (de) * | 2009-09-30 | 2011-03-31 | Bayer Materialscience Ag | Polycarbonatzusammensetzungen mit verbesserten optischen Eigenschaften |
| JP5895339B2 (ja) * | 2009-12-11 | 2016-03-30 | 三菱化学株式会社 | ポリカーボネート樹脂 |
| WO2011083635A1 (ja) * | 2010-01-07 | 2011-07-14 | 出光興産株式会社 | 芳香族ポリカーボネート樹脂組成物及びそれを用いた光学成形品 |
| JP5872905B2 (ja) * | 2012-01-10 | 2016-03-01 | 出光興産株式会社 | 透明熱可塑性樹脂ペレットの製造方法 |
-
2011
- 2011-12-28 JP JP2011290051A patent/JP5879124B2/ja active Active
-
2012
- 2012-12-27 WO PCT/JP2012/083966 patent/WO2013100090A1/ja not_active Ceased
- 2012-12-27 EP EP12861531.7A patent/EP2799200B1/en active Active
- 2012-12-27 KR KR1020147017611A patent/KR101923256B1/ko active Active
- 2012-12-27 US US14/369,487 patent/US9593202B2/en active Active
- 2012-12-27 CN CN201280065278.6A patent/CN104023928B/zh active Active
- 2012-12-28 TW TW101150992A patent/TWI582162B/zh active
Patent Citations (4)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JP2002060609A (ja) | 2000-08-18 | 2002-02-26 | Idemitsu Petrochem Co Ltd | 芳香族ポリカーボネート樹脂組成物および成形品 |
| JP2005096421A (ja) | 2003-09-02 | 2005-04-14 | Mitsubishi Engineering Plastics Corp | 導光板用芳香族ポリカーボネート樹脂ペレット、導光板、導光板の製造方法および面光源体 |
| JP2007204737A (ja) * | 2006-01-06 | 2007-08-16 | Mitsubishi Engineering Plastics Corp | 導光板用芳香族ポリカーボネート樹脂組成物および導光板 |
| JP2008202026A (ja) | 2007-01-24 | 2008-09-04 | Mitsubishi Chemicals Corp | 芳香族ポリカーボネートの製造方法 |
Also Published As
| Publication number | Publication date |
|---|---|
| JP2013139097A (ja) | 2013-07-18 |
| EP2799200B1 (en) | 2019-08-28 |
| US20140364546A1 (en) | 2014-12-11 |
| CN104023928B (zh) | 2017-10-31 |
| EP2799200A1 (en) | 2014-11-05 |
| CN104023928A (zh) | 2014-09-03 |
| JP5879124B2 (ja) | 2016-03-08 |
| KR20140115305A (ko) | 2014-09-30 |
| TW201333109A (zh) | 2013-08-16 |
| US9593202B2 (en) | 2017-03-14 |
| EP2799200A4 (en) | 2015-07-08 |
| TWI582162B (zh) | 2017-05-11 |
| WO2013100090A1 (ja) | 2013-07-04 |
Similar Documents
| Publication | Publication Date | Title |
|---|---|---|
| KR101923256B1 (ko) | 폴리카보네이트 수지 조성물 펠릿 및 그 제조 방법 | |
| KR101479113B1 (ko) | 도광판용 방향족 폴리카보네이트 수지 조성물 및 도광판 | |
| KR101393822B1 (ko) | 광 확산성 수지 조성물 및 그것을 이용한 광 확산판 | |
| CN101193981B (zh) | 光扩散性聚碳酸酯系树脂组合物以及使用该树脂组合物的光扩散板 | |
| KR101393901B1 (ko) | 폴리카보네이트계 수지 조성물, 그것을 이용한 광학 성형체및 조명 유닛 | |
| US7935750B2 (en) | Polycarbonate light diffusing resin composition | |
| JP5266639B2 (ja) | 導光板 | |
| EP2703710B1 (en) | Polycarbonate resin composition for transparent body, as well as transparent body and surface light source formed from same | |
| KR20140105464A (ko) | 방향족 폴리카보네이트 수지 조성물 및 광학 성형품 | |
| JP5005949B2 (ja) | ポリカーボネート系樹脂組成物、光学成形品及び照明ユニット | |
| JP6483340B2 (ja) | 導光性能を有するポリカーボネート樹脂組成物およびそれからなる導光体 | |
| JP5064720B2 (ja) | ポリカーボネート系樹脂組成物、それを用いた光学成形体及び照明ユニット | |
| JP2009040843A (ja) | ポリカーボネート系樹脂組成物及びそれからなる光学成形品 |
Legal Events
| Date | Code | Title | Description |
|---|---|---|---|
| PA0105 | International application |
Patent event date: 20140626 Patent event code: PA01051R01D Comment text: International Patent Application |
|
| PG1501 | Laying open of application | ||
| A201 | Request for examination | ||
| PA0201 | Request for examination |
Patent event code: PA02012R01D Patent event date: 20170921 Comment text: Request for Examination of Application |
|
| E902 | Notification of reason for refusal | ||
| PE0902 | Notice of grounds for rejection |
Comment text: Notification of reason for refusal Patent event date: 20180315 Patent event code: PE09021S01D |
|
| E701 | Decision to grant or registration of patent right | ||
| PE0701 | Decision of registration |
Patent event code: PE07011S01D Comment text: Decision to Grant Registration Patent event date: 20180921 |
|
| GRNT | Written decision to grant | ||
| PR0701 | Registration of establishment |
Comment text: Registration of Establishment Patent event date: 20181122 Patent event code: PR07011E01D |
|
| PR1002 | Payment of registration fee |
Payment date: 20181122 End annual number: 3 Start annual number: 1 |
|
| PG1601 | Publication of registration | ||
| PR1001 | Payment of annual fee |
Payment date: 20211027 Start annual number: 4 End annual number: 4 |
|
| PR1001 | Payment of annual fee |
Payment date: 20221019 Start annual number: 5 End annual number: 5 |
|
| PR1001 | Payment of annual fee |
Payment date: 20231017 Start annual number: 6 End annual number: 6 |
|
| PR1001 | Payment of annual fee |
Payment date: 20241017 Start annual number: 7 End annual number: 7 |