TWI329121B - Poly(ester)carbonate molding compositions - Google Patents
Poly(ester)carbonate molding compositions Download PDFInfo
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- TWI329121B TWI329121B TW92133763A TW92133763A TWI329121B TW I329121 B TWI329121 B TW I329121B TW 92133763 A TW92133763 A TW 92133763A TW 92133763 A TW92133763 A TW 92133763A TW I329121 B TWI329121 B TW I329121B
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- 239000000203 mixture Substances 0.000 title claims description 67
- -1 Poly(ester) Polymers 0.000 title claims description 26
- 238000000465 moulding Methods 0.000 title description 7
- BVKZGUZCCUSVTD-UHFFFAOYSA-L Carbonate Chemical compound [O-]C([O-])=O BVKZGUZCCUSVTD-UHFFFAOYSA-L 0.000 title description 4
- 239000004417 polycarbonate Substances 0.000 claims description 32
- 229920001971 elastomer Polymers 0.000 claims description 29
- 229920000515 polycarbonate Polymers 0.000 claims description 28
- 239000005060 rubber Substances 0.000 claims description 28
- 125000003118 aryl group Chemical group 0.000 claims description 24
- 150000001875 compounds Chemical class 0.000 claims description 20
- 229920000642 polymer Polymers 0.000 claims description 19
- 229920000578 graft copolymer Polymers 0.000 claims description 17
- 239000006085 branching agent Substances 0.000 claims description 15
- 239000011159 matrix material Substances 0.000 claims description 15
- 239000003063 flame retardant Substances 0.000 claims description 14
- 229920000098 polyolefin Polymers 0.000 claims description 14
- 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 claims description 13
- 125000000217 alkyl group Chemical group 0.000 claims description 12
- 239000000052 vinegar Substances 0.000 claims description 12
- 235000021419 vinegar Nutrition 0.000 claims description 12
- 239000002253 acid Substances 0.000 claims description 11
- 239000002131 composite material Substances 0.000 claims description 11
- 239000000178 monomer Substances 0.000 claims description 11
- NLHHRLWOUZZQLW-UHFFFAOYSA-N Acrylonitrile Chemical compound C=CC#N NLHHRLWOUZZQLW-UHFFFAOYSA-N 0.000 claims description 10
- NIXOWILDQLNWCW-UHFFFAOYSA-N acrylic acid group Chemical group C(C=C)(=O)O NIXOWILDQLNWCW-UHFFFAOYSA-N 0.000 claims description 10
- 239000000654 additive Substances 0.000 claims description 10
- 239000003795 chemical substances by application Substances 0.000 claims description 10
- 229920000728 polyester Polymers 0.000 claims description 10
- 239000005977 Ethylene Substances 0.000 claims description 7
- 239000002904 solvent Substances 0.000 claims description 7
- NIXOWILDQLNWCW-UHFFFAOYSA-M Acrylate Chemical compound [O-]C(=O)C=C NIXOWILDQLNWCW-UHFFFAOYSA-M 0.000 claims description 6
- VGGSQFUCUMXWEO-UHFFFAOYSA-N Ethene Chemical compound C=C VGGSQFUCUMXWEO-UHFFFAOYSA-N 0.000 claims description 6
- ISWSIDIOOBJBQZ-UHFFFAOYSA-N phenol group Chemical group C1(=CC=CC=C1)O ISWSIDIOOBJBQZ-UHFFFAOYSA-N 0.000 claims description 6
- 229920002857 polybutadiene Polymers 0.000 claims description 6
- 229920002554 vinyl polymer Polymers 0.000 claims description 6
- 230000000996 additive effect Effects 0.000 claims description 5
- 229920001577 copolymer Polymers 0.000 claims description 5
- 238000007720 emulsion polymerization reaction Methods 0.000 claims description 5
- 229920005989 resin Polymers 0.000 claims description 5
- 239000011347 resin Substances 0.000 claims description 5
- XKZQKPRCPNGNFR-UHFFFAOYSA-N 2-(3-hydroxyphenyl)phenol Chemical compound OC1=CC=CC(C=2C(=CC=CC=2)O)=C1 XKZQKPRCPNGNFR-UHFFFAOYSA-N 0.000 claims description 4
- 150000004649 carbonic acid derivatives Chemical class 0.000 claims description 4
- 239000000835 fiber Substances 0.000 claims description 4
- 239000003381 stabilizer Substances 0.000 claims description 4
- 238000009757 thermoplastic moulding Methods 0.000 claims description 4
- 125000003277 amino group Chemical group 0.000 claims description 3
- 239000000945 filler Substances 0.000 claims description 3
- 229910052698 phosphorus Inorganic materials 0.000 claims description 3
- 239000011574 phosphorus Substances 0.000 claims description 3
- 238000006116 polymerization reaction Methods 0.000 claims description 3
- DAWJJMYZJQJLPZ-UHFFFAOYSA-N 2-sulfanylprop-2-enoic acid Chemical compound OC(=O)C(S)=C DAWJJMYZJQJLPZ-UHFFFAOYSA-N 0.000 claims description 2
- 229920002943 EPDM rubber Polymers 0.000 claims description 2
- 239000006057 Non-nutritive feed additive Substances 0.000 claims description 2
- OAICVXFJPJFONN-UHFFFAOYSA-N Phosphorus Chemical compound [P] OAICVXFJPJFONN-UHFFFAOYSA-N 0.000 claims description 2
- 239000005062 Polybutadiene Substances 0.000 claims description 2
- 239000006096 absorbing agent Substances 0.000 claims description 2
- 239000003963 antioxidant agent Substances 0.000 claims description 2
- 239000002216 antistatic agent Substances 0.000 claims description 2
- 239000007822 coupling agent Substances 0.000 claims description 2
- 239000004611 light stabiliser Substances 0.000 claims description 2
- 239000000314 lubricant Substances 0.000 claims description 2
- 239000006082 mold release agent Substances 0.000 claims description 2
- 239000002667 nucleating agent Substances 0.000 claims description 2
- 239000000049 pigment Substances 0.000 claims description 2
- 239000003755 preservative agent Substances 0.000 claims description 2
- 239000012744 reinforcing agent Substances 0.000 claims description 2
- 150000003304 ruthenium compounds Chemical class 0.000 claims description 2
- 239000000779 smoke Substances 0.000 claims description 2
- 239000003017 thermal stabilizer Substances 0.000 claims description 2
- 150000001735 carboxylic acids Chemical class 0.000 claims 2
- 230000002079 cooperative effect Effects 0.000 claims 2
- 239000004721 Polyphenylene oxide Substances 0.000 claims 1
- 239000004734 Polyphenylene sulfide Substances 0.000 claims 1
- 230000003078 antioxidant effect Effects 0.000 claims 1
- 229920003244 diene elastomer Polymers 0.000 claims 1
- 230000000694 effects Effects 0.000 claims 1
- 150000002118 epoxides Chemical class 0.000 claims 1
- 239000004088 foaming agent Substances 0.000 claims 1
- 230000003301 hydrolyzing effect Effects 0.000 claims 1
- 229920006380 polyphenylene oxide Polymers 0.000 claims 1
- 229920000069 polyphenylene sulfide Polymers 0.000 claims 1
- 230000002335 preservative effect Effects 0.000 claims 1
- 239000002966 varnish Substances 0.000 claims 1
- PPBRXRYQALVLMV-UHFFFAOYSA-N Styrene Chemical compound C=CC1=CC=CC=C1 PPBRXRYQALVLMV-UHFFFAOYSA-N 0.000 description 15
- 239000000839 emulsion Substances 0.000 description 10
- 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 9
- 238000004519 manufacturing process Methods 0.000 description 9
- 238000012360 testing method Methods 0.000 description 9
- OAKJQQAXSVQMHS-UHFFFAOYSA-N Hydrazine Chemical compound NN OAKJQQAXSVQMHS-UHFFFAOYSA-N 0.000 description 8
- 239000007789 gas Substances 0.000 description 8
- YXFVVABEGXRONW-UHFFFAOYSA-N Toluene Chemical compound CC1=CC=CC=C1 YXFVVABEGXRONW-UHFFFAOYSA-N 0.000 description 6
- 238000000034 method Methods 0.000 description 6
- 239000003431 cross linking reagent Substances 0.000 description 5
- 238000001125 extrusion Methods 0.000 description 5
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 description 5
- 239000002245 particle Substances 0.000 description 5
- 239000000243 solution Substances 0.000 description 5
- SMZOUWXMTYCWNB-UHFFFAOYSA-N 2-(2-methoxy-5-methylphenyl)ethanamine Chemical compound COC1=CC=C(C)C=C1CCN SMZOUWXMTYCWNB-UHFFFAOYSA-N 0.000 description 4
- 229940106691 bisphenol a Drugs 0.000 description 4
- 125000004432 carbon atom Chemical group C* 0.000 description 4
- 150000002148 esters Chemical class 0.000 description 4
- 239000001257 hydrogen Substances 0.000 description 4
- 229910052739 hydrogen Inorganic materials 0.000 description 4
- 239000000463 material Substances 0.000 description 4
- BISUFDNSWDVFNB-UHFFFAOYSA-K C(C=C)(=O)[O-].[Ru+3].C(C=C)(=O)[O-].C(C=C)(=O)[O-] Chemical compound C(C=C)(=O)[O-].[Ru+3].C(C=C)(=O)[O-].C(C=C)(=O)[O-] BISUFDNSWDVFNB-UHFFFAOYSA-K 0.000 description 3
- 239000004594 Masterbatch (MB) Substances 0.000 description 3
- CERQOIWHTDAKMF-UHFFFAOYSA-N Methacrylic acid Chemical compound CC(=C)C(O)=O CERQOIWHTDAKMF-UHFFFAOYSA-N 0.000 description 3
- VVQNEPGJFQJSBK-UHFFFAOYSA-N Methyl methacrylate Chemical compound COC(=O)C(C)=C VVQNEPGJFQJSBK-UHFFFAOYSA-N 0.000 description 3
- 229910019142 PO4 Inorganic materials 0.000 description 3
- 150000001335 aliphatic alkanes Chemical class 0.000 description 3
- 125000004429 atom Chemical group 0.000 description 3
- CQEYYJKEWSMYFG-UHFFFAOYSA-N butyl acrylate Chemical compound CCCCOC(=O)C=C CQEYYJKEWSMYFG-UHFFFAOYSA-N 0.000 description 3
- 238000006243 chemical reaction Methods 0.000 description 3
- DIOQZVSQGTUSAI-UHFFFAOYSA-N decane Chemical compound CCCCCCCCCC DIOQZVSQGTUSAI-UHFFFAOYSA-N 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
- 125000004435 hydrogen atom Chemical group [H]* 0.000 description 3
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 description 3
- 239000010452 phosphate Substances 0.000 description 3
- 150000003839 salts Chemical class 0.000 description 3
- PWEBUXCTKOWPCW-UHFFFAOYSA-N squaric acid Chemical compound OC1=C(O)C(=O)C1=O PWEBUXCTKOWPCW-UHFFFAOYSA-N 0.000 description 3
- AZQWKYJCGOJGHM-UHFFFAOYSA-N 1,4-benzoquinone Chemical compound O=C1C=CC(=O)C=C1 AZQWKYJCGOJGHM-UHFFFAOYSA-N 0.000 description 2
- BSWWXRFVMJHFBN-UHFFFAOYSA-N 2,4,6-tribromophenol Chemical compound OC1=C(Br)C=C(Br)C=C1Br BSWWXRFVMJHFBN-UHFFFAOYSA-N 0.000 description 2
- KAKZBPTYRLMSJV-UHFFFAOYSA-N Butadiene Chemical compound C=CC=C KAKZBPTYRLMSJV-UHFFFAOYSA-N 0.000 description 2
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical group [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 description 2
- 239000004215 Carbon black (E152) Substances 0.000 description 2
- KFZMGEQAYNKOFK-UHFFFAOYSA-N Isopropanol Chemical compound CC(C)O KFZMGEQAYNKOFK-UHFFFAOYSA-N 0.000 description 2
- BAPJBEWLBFYGME-UHFFFAOYSA-N Methyl acrylate Chemical compound COC(=O)C=C BAPJBEWLBFYGME-UHFFFAOYSA-N 0.000 description 2
- 125000001931 aliphatic group Chemical group 0.000 description 2
- XYLMUPLGERFSHI-UHFFFAOYSA-N alpha-Methylstyrene Chemical compound CC(=C)C1=CC=CC=C1 XYLMUPLGERFSHI-UHFFFAOYSA-N 0.000 description 2
- 230000008901 benefit Effects 0.000 description 2
- 229910052797 bismuth Inorganic materials 0.000 description 2
- JCXGWMGPZLAOME-UHFFFAOYSA-N bismuth atom Chemical compound [Bi] JCXGWMGPZLAOME-UHFFFAOYSA-N 0.000 description 2
- 229910052799 carbon Inorganic materials 0.000 description 2
- 238000002485 combustion reaction Methods 0.000 description 2
- 238000007796 conventional method Methods 0.000 description 2
- 238000005336 cracking Methods 0.000 description 2
- RWGFKTVRMDUZSP-UHFFFAOYSA-N cumene Chemical compound CC(C)C1=CC=CC=C1 RWGFKTVRMDUZSP-UHFFFAOYSA-N 0.000 description 2
- GTBGXKPAKVYEKJ-UHFFFAOYSA-N decyl 2-methylprop-2-enoate Chemical compound CCCCCCCCCCOC(=O)C(C)=C GTBGXKPAKVYEKJ-UHFFFAOYSA-N 0.000 description 2
- 238000009826 distribution Methods 0.000 description 2
- 238000010101 extrusion blow moulding Methods 0.000 description 2
- 125000000524 functional group Chemical group 0.000 description 2
- 238000002309 gasification Methods 0.000 description 2
- 238000005227 gel permeation chromatography Methods 0.000 description 2
- 125000005842 heteroatom Chemical group 0.000 description 2
- 238000004128 high performance liquid chromatography Methods 0.000 description 2
- 229930195733 hydrocarbon Natural products 0.000 description 2
- 150000002430 hydrocarbons Chemical class 0.000 description 2
- 238000001746 injection moulding Methods 0.000 description 2
- FPYJFEHAWHCUMM-UHFFFAOYSA-N maleic anhydride Chemical compound O=C1OC(=O)C=C1 FPYJFEHAWHCUMM-UHFFFAOYSA-N 0.000 description 2
- 125000000325 methylidene group Chemical group [H]C([H])=* 0.000 description 2
- 125000002950 monocyclic group Chemical group 0.000 description 2
- 150000002923 oximes Chemical class 0.000 description 2
- JRKICGRDRMAZLK-UHFFFAOYSA-L peroxydisulfate Chemical compound [O-]S(=O)(=O)OOS([O-])(=O)=O JRKICGRDRMAZLK-UHFFFAOYSA-L 0.000 description 2
- 239000000843 powder Substances 0.000 description 2
- 238000003672 processing method Methods 0.000 description 2
- FBCQUCJYYPMKRO-UHFFFAOYSA-N prop-2-enyl 2-methylprop-2-enoate Chemical compound CC(=C)C(=O)OCC=C FBCQUCJYYPMKRO-UHFFFAOYSA-N 0.000 description 2
- 239000001294 propane Substances 0.000 description 2
- 150000003254 radicals Chemical class 0.000 description 2
- 230000009467 reduction Effects 0.000 description 2
- GHMLBKRAJCXXBS-UHFFFAOYSA-N resorcinol Chemical compound OC1=CC=CC(O)=C1 GHMLBKRAJCXXBS-UHFFFAOYSA-N 0.000 description 2
- 239000000126 substance Substances 0.000 description 2
- 239000000758 substrate Substances 0.000 description 2
- BFKJFAAPBSQJPD-UHFFFAOYSA-N tetrafluoroethene Chemical group FC(F)=C(F)F BFKJFAAPBSQJPD-UHFFFAOYSA-N 0.000 description 2
- 125000000391 vinyl group Chemical group [H]C([*])=C([H])[H] 0.000 description 2
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 2
- PYOLJOJPIPCRDP-UHFFFAOYSA-N 1,1,3-trimethylcyclohexane Chemical compound CC1CCCC(C)(C)C1 PYOLJOJPIPCRDP-UHFFFAOYSA-N 0.000 description 1
- DIIIISSCIXVANO-UHFFFAOYSA-N 1,2-Dimethylhydrazine Chemical compound CNNC DIIIISSCIXVANO-UHFFFAOYSA-N 0.000 description 1
- VZXTWGWHSMCWGA-UHFFFAOYSA-N 1,3,5-triazine-2,4-diamine Chemical compound NC1=NC=NC(N)=N1 VZXTWGWHSMCWGA-UHFFFAOYSA-N 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
- VDYWHVQKENANGY-UHFFFAOYSA-N 1,3-Butyleneglycol dimethacrylate Chemical compound CC(=C)C(=O)OC(C)CCOC(=O)C(C)=C VDYWHVQKENANGY-UHFFFAOYSA-N 0.000 description 1
- RYHBNJHYFVUHQT-UHFFFAOYSA-N 1,4-Dioxane Chemical compound C1COCCO1 RYHBNJHYFVUHQT-UHFFFAOYSA-N 0.000 description 1
- RMSGQZDGSZOJMU-UHFFFAOYSA-N 1-butyl-2-phenylbenzene Chemical group CCCCC1=CC=CC=C1C1=CC=CC=C1 RMSGQZDGSZOJMU-UHFFFAOYSA-N 0.000 description 1
- LOLANUHFGPZTLQ-UHFFFAOYSA-N 1-ethoxydecane Chemical compound CCCCCCCCCCOCC LOLANUHFGPZTLQ-UHFFFAOYSA-N 0.000 description 1
- ZNRPUQQOHLCOMC-UHFFFAOYSA-N 10,10,10-triethoxydecylbenzene Chemical compound C(C)OC(CCCCCCCCCC1=CC=CC=C1)(OCC)OCC ZNRPUQQOHLCOMC-UHFFFAOYSA-N 0.000 description 1
- WLRWTEIAYJHXDW-UHFFFAOYSA-N 2,2,3,3,4,4,4a,5,5,6-decamethyl-6H-cyclopenta[b]pyran Chemical compound CC1C=C2C(C(C(C(O2)(C)C)(C)C)(C)C)(C1(C)C)C WLRWTEIAYJHXDW-UHFFFAOYSA-N 0.000 description 1
- VXHYVVAUHMGCEX-UHFFFAOYSA-N 2-(2-hydroxyphenoxy)phenol Chemical compound OC1=CC=CC=C1OC1=CC=CC=C1O VXHYVVAUHMGCEX-UHFFFAOYSA-N 0.000 description 1
- XSVZEASGNTZBRQ-UHFFFAOYSA-N 2-(2-hydroxyphenyl)sulfinylphenol Chemical compound OC1=CC=CC=C1S(=O)C1=CC=CC=C1O XSVZEASGNTZBRQ-UHFFFAOYSA-N 0.000 description 1
- JJBFVQSGPLGDNX-UHFFFAOYSA-N 2-(2-methylprop-2-enoyloxy)propyl 2-methylprop-2-enoate Chemical compound CC(=C)C(=O)OC(C)COC(=O)C(C)=C JJBFVQSGPLGDNX-UHFFFAOYSA-N 0.000 description 1
- HIXDQWDOVZUNNA-UHFFFAOYSA-N 2-(3,4-dimethoxyphenyl)-5-hydroxy-7-methoxychromen-4-one Chemical compound C=1C(OC)=CC(O)=C(C(C=2)=O)C=1OC=2C1=CC=C(OC)C(OC)=C1 HIXDQWDOVZUNNA-UHFFFAOYSA-N 0.000 description 1
- ZWEHNKRNPOVVGH-UHFFFAOYSA-N 2-Butanone Chemical compound CCC(C)=O ZWEHNKRNPOVVGH-UHFFFAOYSA-N 0.000 description 1
- YFTHPAKWQBTOLK-UHFFFAOYSA-N 2-ethenyloxane Chemical compound C=CC1CCCCO1 YFTHPAKWQBTOLK-UHFFFAOYSA-N 0.000 description 1
- WDQMWEYDKDCEHT-UHFFFAOYSA-N 2-ethylhexyl 2-methylprop-2-enoate Chemical compound CCCCC(CC)COC(=O)C(C)=C WDQMWEYDKDCEHT-UHFFFAOYSA-N 0.000 description 1
- FIWYWGLEPWBBQU-UHFFFAOYSA-N 2-heptylphenol Chemical compound CCCCCCCC1=CC=CC=C1O FIWYWGLEPWBBQU-UHFFFAOYSA-N 0.000 description 1
- KXGFMDJXCMQABM-UHFFFAOYSA-N 2-methoxy-6-methylphenol Chemical compound [CH]OC1=CC=CC([CH])=C1O KXGFMDJXCMQABM-UHFFFAOYSA-N 0.000 description 1
- GTJOHISYCKPIMT-UHFFFAOYSA-N 2-methylundecane Chemical compound CCCCCCCCCC(C)C GTJOHISYCKPIMT-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
- 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
- JLBJTVDPSNHSKJ-UHFFFAOYSA-N 4-Methylstyrene Chemical compound CC1=CC=C(C=C)C=C1 JLBJTVDPSNHSKJ-UHFFFAOYSA-N 0.000 description 1
- KSYGTCNPCHQRKM-UHFFFAOYSA-N 4-[2-(4-hydroxyphenyl)propan-2-yl]phenol Chemical compound C=1C=C(O)C=CC=1C(C)(C)C1=CC=C(O)C=C1.C=1C=C(O)C=CC=1C(C)(C)C1=CC=C(O)C=C1 KSYGTCNPCHQRKM-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
- QHPQWRBYOIRBIT-UHFFFAOYSA-N 4-tert-butylphenol Chemical compound CC(C)(C)C1=CC=C(O)C=C1 QHPQWRBYOIRBIT-UHFFFAOYSA-N 0.000 description 1
- RWHRFHQRVDUPIK-UHFFFAOYSA-N 50867-57-7 Chemical compound CC(=C)C(O)=O.CC(=C)C(O)=O RWHRFHQRVDUPIK-UHFFFAOYSA-N 0.000 description 1
- 229930185605 Bisphenol Natural products 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
- WKBOTKDWSSQWDR-UHFFFAOYSA-N Bromine atom Chemical compound [Br] WKBOTKDWSSQWDR-UHFFFAOYSA-N 0.000 description 1
- NHQRZTMPOQBJMA-UHFFFAOYSA-N C(C)OC(OCC)C(CCCCCCCCC)CCC Chemical compound C(C)OC(OCC)C(CCCCCCCCC)CCC NHQRZTMPOQBJMA-UHFFFAOYSA-N 0.000 description 1
- UTKSASKBBMBPBU-UHFFFAOYSA-N C(CC)C(CCCC(CCCCC)(OC)OC)C Chemical compound C(CC)C(CCCC(CCCCC)(OC)OC)C UTKSASKBBMBPBU-UHFFFAOYSA-N 0.000 description 1
- PVXLNYCCPHJLIA-UHFFFAOYSA-N C(CCCCCCCCC)OCCCCCCCCCC.C=CC Chemical compound C(CCCCCCCCC)OCCCCCCCCCC.C=CC PVXLNYCCPHJLIA-UHFFFAOYSA-N 0.000 description 1
- 125000006539 C12 alkyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])* 0.000 description 1
- BSXNNLKNPUYNMK-UHFFFAOYSA-N CC(C)(C1=COC(OC1)C2=CC=CC=C2)C3=COC(OC3)C4=CC=CC=C4 Chemical compound CC(C)(C1=COC(OC1)C2=CC=CC=C2)C3=COC(OC3)C4=CC=CC=C4 BSXNNLKNPUYNMK-UHFFFAOYSA-N 0.000 description 1
- ZWFHKPNKSWKAOY-UHFFFAOYSA-N CCCCCCCCCCC(C(CCCCCCCC)C1=CC=C(C=C1)C=C)(OC)OC Chemical compound CCCCCCCCCCC(C(CCCCCCCC)C1=CC=C(C=C1)C=C)(OC)OC ZWFHKPNKSWKAOY-UHFFFAOYSA-N 0.000 description 1
- ZCRHCHOHWXDDGH-UHFFFAOYSA-N CCCCCCCCCCC(OC)(OC)OC Chemical compound CCCCCCCCCCC(OC)(OC)OC ZCRHCHOHWXDDGH-UHFFFAOYSA-N 0.000 description 1
- HAYZIMZVUKDFGW-UHFFFAOYSA-N CCCCOOS(O)(=O)=O Chemical compound CCCCOOS(O)(=O)=O HAYZIMZVUKDFGW-UHFFFAOYSA-N 0.000 description 1
- 229920000049 Carbon (fiber) Polymers 0.000 description 1
- VEXZGXHMUGYJMC-UHFFFAOYSA-M Chloride anion Chemical compound [Cl-] VEXZGXHMUGYJMC-UHFFFAOYSA-M 0.000 description 1
- 241000218691 Cupressaceae Species 0.000 description 1
- XFXPMWWXUTWYJX-UHFFFAOYSA-N Cyanide Chemical compound N#[C-] XFXPMWWXUTWYJX-UHFFFAOYSA-N 0.000 description 1
- JIGUQPWFLRLWPJ-UHFFFAOYSA-N Ethyl acrylate Chemical compound CCOC(=O)C=C JIGUQPWFLRLWPJ-UHFFFAOYSA-N 0.000 description 1
- IAYPIBMASNFSPL-UHFFFAOYSA-N Ethylene oxide Chemical compound C1CO1 IAYPIBMASNFSPL-UHFFFAOYSA-N 0.000 description 1
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 description 1
- MHAJPDPJQMAIIY-UHFFFAOYSA-N Hydrogen peroxide Chemical compound OO MHAJPDPJQMAIIY-UHFFFAOYSA-N 0.000 description 1
- 235000000177 Indigofera tinctoria Nutrition 0.000 description 1
- OFOBLEOULBTSOW-UHFFFAOYSA-N Malonic acid Chemical compound OC(=O)CC(O)=O OFOBLEOULBTSOW-UHFFFAOYSA-N 0.000 description 1
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- C08L83/04—Polysiloxanes
-
- Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y02—TECHNOLOGIES OR APPLICATIONS FOR MITIGATION OR ADAPTATION AGAINST CLIMATE CHANGE
- Y02P—CLIMATE CHANGE MITIGATION TECHNOLOGIES IN THE PRODUCTION OR PROCESSING OF GOODS
- Y02P20/00—Technologies relating to chemical industry
- Y02P20/10—Process efficiency
-
- Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y02—TECHNOLOGIES OR APPLICATIONS FOR MITIGATION OR ADAPTATION AGAINST CLIMATE CHANGE
- Y02W—CLIMATE CHANGE MITIGATION TECHNOLOGIES RELATED TO WASTEWATER TREATMENT OR WASTE MANAGEMENT
- Y02W10/00—Technologies for wastewater treatment
- Y02W10/30—Wastewater or sewage treatment systems using renewable energies
- Y02W10/37—Wastewater or sewage treatment systems using renewable energies using solar energy
Landscapes
- Chemical & Material Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Health & Medical Sciences (AREA)
- Medicinal Chemistry (AREA)
- Polymers & Plastics (AREA)
- Organic Chemistry (AREA)
- Engineering & Computer Science (AREA)
- Automation & Control Theory (AREA)
- Compositions Of Macromolecular Compounds (AREA)
- Distillation Of Fermentation Liquor, Processing Of Alcohols, Vinegar And Beer (AREA)
- Vaporization, Distillation, Condensation, Sublimation, And Cold Traps (AREA)
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| DE2002156316 DE10256316A1 (de) | 2002-12-03 | 2002-12-03 | Polycarbonat-Formmassen |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| TW200426179A TW200426179A (en) | 2004-12-01 |
| TWI329121B true TWI329121B (en) | 2010-08-21 |
Family
ID=32335914
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| TW92133763A TWI329121B (en) | 2002-12-03 | 2003-12-02 | Poly(ester)carbonate molding compositions |
Country Status (13)
| Country | Link |
|---|---|
| US (2) | US20040108196A1 (enExample) |
| EP (1) | EP1569995B1 (enExample) |
| JP (1) | JP4398871B2 (enExample) |
| KR (1) | KR100986016B1 (enExample) |
| CN (1) | CN100582150C (enExample) |
| AU (1) | AU2003298126A1 (enExample) |
| BR (1) | BR0316984B1 (enExample) |
| CA (1) | CA2507928C (enExample) |
| DE (2) | DE10256316A1 (enExample) |
| ES (1) | ES2294362T3 (enExample) |
| MX (1) | MXPA05005974A (enExample) |
| TW (1) | TWI329121B (enExample) |
| WO (1) | WO2004050755A1 (enExample) |
Families Citing this family (11)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| DE10036057A1 (de) * | 2000-07-25 | 2002-02-07 | Bayer Ag | Flammwidrige Polycarbonat-Zusammensetzungen |
| WO2007001130A1 (en) * | 2005-06-29 | 2007-01-04 | Cheil Industries Inc. | Polycarbonate resin composition having good chemical resistance and flowability |
| US7446144B2 (en) * | 2005-09-14 | 2008-11-04 | Bayer Materialscience Llc | Thermoplastic molding composition and articles thermoformed therefrom |
| KR100838451B1 (ko) * | 2005-12-30 | 2008-06-16 | 제일모직주식회사 | 내열도가 높고, 내충격성이 우수한 난연성 폴리카보네이트수지 조성물 |
| DE102006012990A1 (de) * | 2006-03-22 | 2007-09-27 | Bayer Materialscience Ag | Flammgeschützte schlagzähmodifizierte Polycarbonat-Zusammensetzungen |
| JP5398843B2 (ja) * | 2008-12-08 | 2014-01-29 | サビック・イノベーティブ・プラスチックス・アイピー・ベスローテン・フェンノートシャップ | 難燃性ポリカーボネート組成物、その製造方法、およびその物品 |
| TWI418883B (zh) * | 2010-03-17 | 2013-12-11 | Au Optronics Corp | 修補方法以及主動元件陣列基板 |
| US8218291B2 (en) * | 2010-03-31 | 2012-07-10 | General Electric Company | Monomers for preparing polycarbonate resins, methods of preparing the monomers, polycarbonate resins prepared with the monomers, and capacitors comprising the polycarbonate resins |
| KR101499246B1 (ko) * | 2012-08-06 | 2015-03-05 | 제일모직주식회사 | 분지형 폴리카보네이트 수지 및 그 제조방법 |
| KR102316905B1 (ko) | 2017-03-10 | 2021-10-25 | 어드밴식스 레진즈 앤드 케미컬즈 엘엘씨 | 개선된 가공성 및 특성을 위한 pa6/66 공중합체 베이스 수지의 와이어 및 케이블 피복 조성물 |
| CN112546659B (zh) * | 2020-12-08 | 2022-02-15 | 云南临沧鑫圆锗业股份有限公司 | 一种四氟化锗的提纯装置及方法 |
Family Cites Families (24)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US3946495A (en) * | 1973-12-19 | 1976-03-30 | Asriel Osdor | Method and apparatus for drying moisture-containing solids particularly domestic refuse and sludge cakes |
| JPS50109247A (ja) | 1974-02-04 | 1975-08-28 | Sumitomo Chemical Co | Netsukasoseijushisoseibutsu |
| US4185009A (en) * | 1975-01-03 | 1980-01-22 | Bayer Aktiengesellschaft | Branched, high-molecular weight thermoplastic polycarbonates |
| JPS5661446A (en) * | 1979-10-24 | 1981-05-26 | Ajinomoto Co Inc | Stabilizer for halogen-containing resin |
| US4358346A (en) * | 1981-05-06 | 1982-11-09 | The Foxboro Company | Control of alcohol distillation |
| JPS5898354A (ja) | 1981-12-07 | 1983-06-11 | Sumitomo Naugatuck Co Ltd | 熱可塑性樹脂組成物 |
| DE3149812A1 (de) | 1981-12-16 | 1983-07-21 | Basf Ag, 6700 Ludwigshafen | Thermoplastische formmassen |
| JPH0796110B2 (ja) * | 1986-04-04 | 1995-10-18 | コニカ株式会社 | 写真処理廃液処理方法及びその装置 |
| US5068285A (en) * | 1989-03-08 | 1991-11-26 | The Dow Chemical Company | Molding compositions with acrylonitrile-styrene-acrylate rubber copolymers |
| US5087663A (en) * | 1989-03-08 | 1992-02-11 | The Dow Chemical Company | Molding compositions with methyl (meth)acrylate-butadiene-styrene graft copolymers |
| DE3924493A1 (de) * | 1989-07-25 | 1991-01-31 | Bayer Ag | Flammwidrige mischungen |
| DE69231876T2 (de) | 1991-01-24 | 2001-10-18 | Idemitsu Petrochemical Co., Ltd. | Polymermischung, die ein verzweigtes Polycarbonat enthält |
| US5314949A (en) * | 1991-01-24 | 1994-05-24 | Idemitsu Petrochemical Co., Ltd. | Polycarbonate resin composition |
| US5258432A (en) * | 1992-03-10 | 1993-11-02 | The Dow Chemical Company | Ignition resistant polycarbonate blends |
| JPH08319406A (ja) * | 1995-05-26 | 1996-12-03 | Kanegafuchi Chem Ind Co Ltd | 難燃性樹脂組成物 |
| TWI234574B (en) * | 1997-05-06 | 2005-06-21 | Idemitsu Kosan Co | Battery pack obtained from a flame-retardant polycarbonate resin composition |
| DE19801198A1 (de) * | 1998-01-15 | 1999-07-22 | Bayer Ag | Flammwidrige Polycarbonat-ABS-Formmassen |
| EP1076675A1 (en) | 1998-05-01 | 2001-02-21 | General Electric Company | Flame retardant polycarbonate/rubber-modified graft copolymer resin blends having a low fluorine content |
| DE69805447T2 (de) * | 1998-06-30 | 2003-01-16 | Centre De Recherche Industrielle Du Quebec, Ste-Foy | Verfahren zur biologischen abwasser- und abgasreinigung und biofilter dafür |
| CA2346711C (en) * | 1998-10-20 | 2003-12-30 | Kevin Lee Kott | Laundry detergents comprising modified alkylbenzene sulfonates |
| JP4627833B2 (ja) * | 2000-02-10 | 2011-02-09 | 旭化成ケミカルズ株式会社 | ポリカーボネート組成物 |
| AU2001287732A1 (en) * | 2000-09-26 | 2002-04-08 | Bayer Aktiengesellschaft | Copolycarbonate-based composition |
| DE10119681A1 (de) * | 2001-04-20 | 2002-10-24 | Bayer Ag | Schlagzähmodifizierte Blends aus Polyethylenenterephthalat und mindestens einem auf Dihydtoxydlarylcyclohexan basierenden Polycarbonat |
| DE10162747A1 (de) * | 2001-12-20 | 2003-07-03 | Bayer Ag | Extrudierbare Polycarbonat-Formmassen |
-
2002
- 2002-12-03 DE DE2002156316 patent/DE10256316A1/de not_active Withdrawn
-
2003
- 2003-11-20 EP EP20030795829 patent/EP1569995B1/de not_active Expired - Lifetime
- 2003-11-20 AU AU2003298126A patent/AU2003298126A1/en not_active Abandoned
- 2003-11-20 CN CN200380104975A patent/CN100582150C/zh not_active Expired - Fee Related
- 2003-11-20 CA CA 2507928 patent/CA2507928C/en not_active Expired - Fee Related
- 2003-11-20 BR BR0316984A patent/BR0316984B1/pt not_active IP Right Cessation
- 2003-11-20 ES ES03795829T patent/ES2294362T3/es not_active Expired - Lifetime
- 2003-11-20 JP JP2004556161A patent/JP4398871B2/ja not_active Expired - Fee Related
- 2003-11-20 MX MXPA05005974A patent/MXPA05005974A/es active IP Right Grant
- 2003-11-20 DE DE50308665T patent/DE50308665D1/de not_active Expired - Lifetime
- 2003-11-20 WO PCT/EP2003/012994 patent/WO2004050755A1/de not_active Ceased
- 2003-11-20 KR KR20057009981A patent/KR100986016B1/ko not_active Expired - Fee Related
- 2003-12-01 US US10/726,210 patent/US20040108196A1/en not_active Abandoned
- 2003-12-01 US US10/725,210 patent/US7186767B2/en not_active Expired - Lifetime
- 2003-12-02 TW TW92133763A patent/TWI329121B/zh not_active IP Right Cessation
Also Published As
| Publication number | Publication date |
|---|---|
| EP1569995A1 (de) | 2005-09-07 |
| KR20050085295A (ko) | 2005-08-29 |
| US20040106731A1 (en) | 2004-06-03 |
| JP4398871B2 (ja) | 2010-01-13 |
| US20040108196A1 (en) | 2004-06-10 |
| WO2004050755A1 (de) | 2004-06-17 |
| DE10256316A1 (de) | 2004-06-24 |
| US7186767B2 (en) | 2007-03-06 |
| DE50308665D1 (de) | 2008-01-03 |
| BR0316984A (pt) | 2005-10-25 |
| BR0316984B1 (pt) | 2013-10-22 |
| EP1569995B1 (de) | 2007-11-21 |
| AU2003298126A1 (en) | 2004-06-23 |
| CN1720290A (zh) | 2006-01-11 |
| KR100986016B1 (ko) | 2010-10-06 |
| ES2294362T3 (es) | 2008-04-01 |
| JP2006509065A (ja) | 2006-03-16 |
| MXPA05005974A (es) | 2005-08-18 |
| TW200426179A (en) | 2004-12-01 |
| CA2507928C (en) | 2012-05-29 |
| CN100582150C (zh) | 2010-01-20 |
| CA2507928A1 (en) | 2004-06-17 |
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Legal Events
| Date | Code | Title | Description |
|---|---|---|---|
| MM4A | Annulment or lapse of patent due to non-payment of fees |