TWI554546B - 聚碳酸酯之製造方法 - Google Patents
聚碳酸酯之製造方法 Download PDFInfo
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- TWI554546B TWI554546B TW102140657A TW102140657A TWI554546B TW I554546 B TWI554546 B TW I554546B TW 102140657 A TW102140657 A TW 102140657A TW 102140657 A TW102140657 A TW 102140657A TW I554546 B TWI554546 B TW I554546B
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- Prior art keywords
- polycarbonate
- reactor
- dihydroxy compound
- temperature
- reaction
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- 229920000515 polycarbonate Polymers 0.000 title claims description 194
- 239000004417 polycarbonate Substances 0.000 title claims description 194
- 238000004519 manufacturing process Methods 0.000 title claims description 38
- 150000001875 compounds Chemical class 0.000 claims description 175
- 238000003756 stirring Methods 0.000 claims description 171
- 238000006068 polycondensation reaction Methods 0.000 claims description 100
- 238000000034 method Methods 0.000 claims description 66
- 230000000052 comparative effect Effects 0.000 claims description 64
- -1 alkylene glycol Chemical compound 0.000 claims description 57
- 125000002723 alicyclic group Chemical group 0.000 claims description 37
- 238000010438 heat treatment Methods 0.000 claims description 37
- 150000004650 carbonic acid diesters Chemical class 0.000 claims description 32
- LYCAIKOWRPUZTN-UHFFFAOYSA-N ethylene glycol Natural products OCCO LYCAIKOWRPUZTN-UHFFFAOYSA-N 0.000 claims description 19
- 125000003118 aryl group Chemical group 0.000 claims description 16
- 239000000203 mixture Substances 0.000 claims description 16
- 125000005647 linker group Chemical group 0.000 claims description 13
- WGCNASOHLSPBMP-UHFFFAOYSA-N hydroxyacetaldehyde Natural products OCC=O WGCNASOHLSPBMP-UHFFFAOYSA-N 0.000 claims description 10
- 125000001931 aliphatic group Chemical group 0.000 claims description 9
- 125000001033 ether group Chemical group 0.000 claims description 2
- 150000002334 glycols Chemical class 0.000 claims description 2
- 125000004122 cyclic group Chemical group 0.000 claims 1
- 239000002994 raw material Substances 0.000 description 81
- 238000006243 chemical reaction Methods 0.000 description 76
- FBPFZTCFMRRESA-FSIIMWSLSA-N D-Glucitol Natural products OC[C@H](O)[C@H](O)[C@@H](O)[C@H](O)CO FBPFZTCFMRRESA-FSIIMWSLSA-N 0.000 description 52
- BDAGIHXWWSANSR-UHFFFAOYSA-N methanoic acid Natural products OC=O BDAGIHXWWSANSR-UHFFFAOYSA-N 0.000 description 52
- 239000000600 sorbitol Substances 0.000 description 52
- 238000006116 polymerization reaction Methods 0.000 description 50
- FBPFZTCFMRRESA-JGWLITMVSA-N D-glucitol Chemical compound OC[C@H](O)[C@@H](O)[C@H](O)[C@H](O)CO FBPFZTCFMRRESA-JGWLITMVSA-N 0.000 description 48
- ISWSIDIOOBJBQZ-UHFFFAOYSA-N Phenol Chemical compound OC1=CC=CC=C1 ISWSIDIOOBJBQZ-UHFFFAOYSA-N 0.000 description 38
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- 239000000155 melt Substances 0.000 description 29
- ROORDVPLFPIABK-UHFFFAOYSA-N diphenyl carbonate Chemical compound C=1C=CC=CC=1OC(=O)OC1=CC=CC=C1 ROORDVPLFPIABK-UHFFFAOYSA-N 0.000 description 27
- OSWFIVFLDKOXQC-UHFFFAOYSA-N 4-(3-methoxyphenyl)aniline Chemical compound COC1=CC=CC(C=2C=CC(N)=CC=2)=C1 OSWFIVFLDKOXQC-UHFFFAOYSA-N 0.000 description 26
- 235000019253 formic acid Nutrition 0.000 description 26
- 239000000463 material Substances 0.000 description 26
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- 239000003054 catalyst Substances 0.000 description 24
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- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 description 23
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- 230000009477 glass transition Effects 0.000 description 22
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- IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 description 17
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- OTLDLKLSNZMTTA-UHFFFAOYSA-N octahydro-1h-4,7-methanoindene-1,5-diyldimethanol Chemical compound C1C2C3C(CO)CCC3C1C(CO)C2 OTLDLKLSNZMTTA-UHFFFAOYSA-N 0.000 description 17
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- 239000000178 monomer Substances 0.000 description 10
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- 229910000147 aluminium phosphate Inorganic materials 0.000 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 description 9
- 229910052757 nitrogen Inorganic materials 0.000 description 9
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- BXGYYDRIMBPOMN-UHFFFAOYSA-N 2-(hydroxymethoxy)ethoxymethanol Chemical compound OCOCCOCO BXGYYDRIMBPOMN-UHFFFAOYSA-N 0.000 description 8
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- YXFVVABEGXRONW-UHFFFAOYSA-N Toluene Chemical compound CC1=CC=CC=C1 YXFVVABEGXRONW-UHFFFAOYSA-N 0.000 description 7
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- 230000006866 deterioration Effects 0.000 description 7
- 238000004898 kneading Methods 0.000 description 7
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- CSCPPACGZOOCGX-UHFFFAOYSA-N Acetone Chemical compound CC(C)=O CSCPPACGZOOCGX-UHFFFAOYSA-N 0.000 description 6
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- XKRFYHLGVUSROY-UHFFFAOYSA-N Argon Chemical compound [Ar] XKRFYHLGVUSROY-UHFFFAOYSA-N 0.000 description 6
- HEDRZPFGACZZDS-UHFFFAOYSA-N Chloroform Chemical compound ClC(Cl)Cl HEDRZPFGACZZDS-UHFFFAOYSA-N 0.000 description 6
- YMWUJEATGCHHMB-UHFFFAOYSA-N Dichloromethane Chemical compound ClCCl YMWUJEATGCHHMB-UHFFFAOYSA-N 0.000 description 6
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- 229910052751 metal Inorganic materials 0.000 description 6
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- 239000003017 thermal stabilizer Substances 0.000 description 6
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 5
- 230000015572 biosynthetic process Effects 0.000 description 5
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- 235000014113 dietary fatty acids Nutrition 0.000 description 5
- 238000001704 evaporation Methods 0.000 description 5
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- 238000001746 injection moulding Methods 0.000 description 5
- 239000008188 pellet Substances 0.000 description 5
- 238000011002 quantification Methods 0.000 description 5
- 150000003839 salts Chemical class 0.000 description 5
- QPFMBZIOSGYJDE-UHFFFAOYSA-N 1,1,2,2-tetrachloroethane Chemical compound ClC(Cl)C(Cl)Cl QPFMBZIOSGYJDE-UHFFFAOYSA-N 0.000 description 4
- VTYYLEPIZMXCLO-UHFFFAOYSA-L Calcium carbonate Chemical class [Ca+2].[O-]C([O-])=O VTYYLEPIZMXCLO-UHFFFAOYSA-L 0.000 description 4
- SIKJAQJRHWYJAI-UHFFFAOYSA-N Indole Chemical compound C1=CC=C2NC=CC2=C1 SIKJAQJRHWYJAI-UHFFFAOYSA-N 0.000 description 4
- UHOVQNZJYSORNB-UHFFFAOYSA-N benzene Substances C1=CC=CC=C1 UHOVQNZJYSORNB-UHFFFAOYSA-N 0.000 description 4
- NNBZCPXTIHJBJL-UHFFFAOYSA-N decalin Chemical compound C1CCCC2CCCCC21 NNBZCPXTIHJBJL-UHFFFAOYSA-N 0.000 description 4
- 238000009792 diffusion process Methods 0.000 description 4
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- 238000007086 side reaction Methods 0.000 description 4
- 238000012360 testing method Methods 0.000 description 4
- 238000012546 transfer Methods 0.000 description 4
- WVLBCYQITXONBZ-UHFFFAOYSA-N trimethyl phosphate Chemical compound COP(=O)(OC)OC WVLBCYQITXONBZ-UHFFFAOYSA-N 0.000 description 4
- 238000005160 1H NMR spectroscopy Methods 0.000 description 3
- ORILYTVJVMAKLC-UHFFFAOYSA-N Adamantane Natural products C1C(C2)CC3CC1CC2C3 ORILYTVJVMAKLC-UHFFFAOYSA-N 0.000 description 3
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- KJTLSVCANCCWHF-UHFFFAOYSA-N Ruthenium Chemical compound [Ru] KJTLSVCANCCWHF-UHFFFAOYSA-N 0.000 description 3
- 235000021355 Stearic acid Nutrition 0.000 description 3
- YIMQCDZDWXUDCA-UHFFFAOYSA-N [4-(hydroxymethyl)cyclohexyl]methanol Chemical compound OCC1CCC(CO)CC1 YIMQCDZDWXUDCA-UHFFFAOYSA-N 0.000 description 3
- 229910052783 alkali metal Inorganic materials 0.000 description 3
- 239000003963 antioxidant agent Substances 0.000 description 3
- 229910052786 argon Inorganic materials 0.000 description 3
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- 125000004429 atom Chemical group 0.000 description 3
- ITHZDDVSAWDQPZ-UHFFFAOYSA-L barium acetate Chemical compound [Ba+2].CC([O-])=O.CC([O-])=O ITHZDDVSAWDQPZ-UHFFFAOYSA-L 0.000 description 3
- RQPZNWPYLFFXCP-UHFFFAOYSA-L barium dihydroxide Chemical compound [OH-].[OH-].[Ba+2] RQPZNWPYLFFXCP-UHFFFAOYSA-L 0.000 description 3
- 229910001863 barium hydroxide Inorganic materials 0.000 description 3
- UCVMQZHZWWEPRC-UHFFFAOYSA-L barium(2+);hydrogen carbonate Chemical compound [Ba+2].OC([O-])=O.OC([O-])=O UCVMQZHZWWEPRC-UHFFFAOYSA-L 0.000 description 3
- AGXUVMPSUKZYDT-UHFFFAOYSA-L barium(2+);octadecanoate Chemical compound [Ba+2].CCCCCCCCCCCCCCCCCC([O-])=O.CCCCCCCCCCCCCCCCCC([O-])=O AGXUVMPSUKZYDT-UHFFFAOYSA-L 0.000 description 3
- 239000002585 base Substances 0.000 description 3
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- MTHSVFCYNBDYFN-UHFFFAOYSA-N diethylene glycol Chemical compound OCCOCCO MTHSVFCYNBDYFN-UHFFFAOYSA-N 0.000 description 3
- 150000004665 fatty acids Chemical class 0.000 description 3
- 125000004435 hydrogen atom Chemical group [H]* 0.000 description 3
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- SYSQUGFVNFXIIT-UHFFFAOYSA-N n-[4-(1,3-benzoxazol-2-yl)phenyl]-4-nitrobenzenesulfonamide Chemical class C1=CC([N+](=O)[O-])=CC=C1S(=O)(=O)NC1=CC=C(C=2OC3=CC=CC=C3N=2)C=C1 SYSQUGFVNFXIIT-UHFFFAOYSA-N 0.000 description 3
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- XZZNDPSIHUTMOC-UHFFFAOYSA-N triphenyl phosphate Chemical compound C=1C=CC=CC=1OP(OC=1C=CC=CC=1)(=O)OC1=CC=CC=C1 XZZNDPSIHUTMOC-UHFFFAOYSA-N 0.000 description 3
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- NNJPAMQRBHASEV-UHFFFAOYSA-N (2-phosphonophenyl)phosphonic acid Chemical compound OP(O)(=O)C1=CC=CC=C1P(O)(O)=O NNJPAMQRBHASEV-UHFFFAOYSA-N 0.000 description 2
- CYOQTWZWFHXPDM-UHFFFAOYSA-N (2-tridecylphenyl) dihydrogen phosphate Chemical compound CCCCCCCCCCCCCc1ccccc1OP(O)(O)=O CYOQTWZWFHXPDM-UHFFFAOYSA-N 0.000 description 2
- KLDXJTOLSGUMSJ-UNTFVMJOSA-N (3s,3ar,6s,6ar)-2,3,3a,5,6,6a-hexahydrofuro[3,2-b]furan-3,6-diol Chemical compound O[C@H]1CO[C@@H]2[C@@H](O)CO[C@@H]21 KLDXJTOLSGUMSJ-UNTFVMJOSA-N 0.000 description 2
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- NCMRSHZOFGKWRG-UHFFFAOYSA-N 2-[4-[9-[4-(2-hydroxyethoxy)phenyl]-10h-anthracen-9-yl]phenoxy]ethanol Chemical compound C1=CC(OCCO)=CC=C1C1(C=2C=CC(OCCO)=CC=2)C2=CC=CC=C2CC2=CC=CC=C21 NCMRSHZOFGKWRG-UHFFFAOYSA-N 0.000 description 2
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- 239000002028 Biomass Substances 0.000 description 2
- CURLTUGMZLYLDI-UHFFFAOYSA-N Carbon dioxide Chemical compound O=C=O CURLTUGMZLYLDI-UHFFFAOYSA-N 0.000 description 2
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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 2
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- PFURGBBHAOXLIO-UHFFFAOYSA-N cyclohexane-1,2-diol Chemical compound OC1CCCCC1O PFURGBBHAOXLIO-UHFFFAOYSA-N 0.000 description 2
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- IPCSVZSSVZVIGE-UHFFFAOYSA-N hexadecanoic acid Chemical compound CCCCCCCCCCCCCCCC(O)=O IPCSVZSSVZVIGE-UHFFFAOYSA-N 0.000 description 2
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- 229910052739 hydrogen Inorganic materials 0.000 description 2
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- NVTNQIBQPLGHGE-UHFFFAOYSA-N n,n-dibutylbutan-1-amine;hydrate Chemical compound [OH-].CCCC[NH+](CCCC)CCCC NVTNQIBQPLGHGE-UHFFFAOYSA-N 0.000 description 1
- JEUXZUSUYIHGNL-UHFFFAOYSA-N n,n-diethylethanamine;hydrate Chemical compound O.CCN(CC)CC JEUXZUSUYIHGNL-UHFFFAOYSA-N 0.000 description 1
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- 238000006864 oxidative decomposition reaction Methods 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
- WXZMFSXDPGVJKK-UHFFFAOYSA-N pentaerythritol Chemical compound OCC(CO)(CO)CO WXZMFSXDPGVJKK-UHFFFAOYSA-N 0.000 description 1
- 230000000737 periodic effect Effects 0.000 description 1
- 150000002989 phenols Chemical class 0.000 description 1
- WKJXXIJJVMOWCA-UHFFFAOYSA-N phenyl dipropan-2-yl phosphate Chemical compound CC(C)OP(=O)(OC(C)C)OC1=CC=CC=C1 WKJXXIJJVMOWCA-UHFFFAOYSA-N 0.000 description 1
- KEWQEYWDKQFKLA-UHFFFAOYSA-N phenyl tridecyl hydrogen phosphate Chemical compound CCCCCCCCCCCCCOP(O)(=O)OC1=CC=CC=C1 KEWQEYWDKQFKLA-UHFFFAOYSA-N 0.000 description 1
- NBIIXXVUZAFLBC-UHFFFAOYSA-K phosphate Chemical compound [O-]P([O-])([O-])=O NBIIXXVUZAFLBC-UHFFFAOYSA-K 0.000 description 1
- 239000010452 phosphate Substances 0.000 description 1
- ACVYVLVWPXVTIT-UHFFFAOYSA-N phosphinic acid Chemical compound O[PH2]=O ACVYVLVWPXVTIT-UHFFFAOYSA-N 0.000 description 1
- 150000004714 phosphonium salts Chemical group 0.000 description 1
- 150000003013 phosphoric acid derivatives Chemical class 0.000 description 1
- 229920000747 poly(lactic acid) Polymers 0.000 description 1
- 229920002647 polyamide Polymers 0.000 description 1
- 229920002961 polybutylene succinate Polymers 0.000 description 1
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- 229920001228 polyisocyanate Polymers 0.000 description 1
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- 229920002223 polystyrene Polymers 0.000 description 1
- 229920000166 polytrimethylene carbonate Polymers 0.000 description 1
- 235000011056 potassium acetate Nutrition 0.000 description 1
- XAEFZNCEHLXOMS-UHFFFAOYSA-M potassium benzoate Chemical compound [K+].[O-]C(=O)C1=CC=CC=C1 XAEFZNCEHLXOMS-UHFFFAOYSA-M 0.000 description 1
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- 229940103091 potassium benzoate Drugs 0.000 description 1
- 229910000028 potassium bicarbonate Inorganic materials 0.000 description 1
- 235000015497 potassium bicarbonate Nutrition 0.000 description 1
- 239000011736 potassium bicarbonate Substances 0.000 description 1
- 229910000027 potassium carbonate Inorganic materials 0.000 description 1
- 235000011181 potassium carbonates Nutrition 0.000 description 1
- TYJJADVDDVDEDZ-UHFFFAOYSA-M potassium hydrogencarbonate Chemical compound [K+].OC([O-])=O TYJJADVDDVDEDZ-UHFFFAOYSA-M 0.000 description 1
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- ANBFRLKBEIFNQU-UHFFFAOYSA-M potassium;octadecanoate Chemical compound [K+].CCCCCCCCCCCCCCCCCC([O-])=O ANBFRLKBEIFNQU-UHFFFAOYSA-M 0.000 description 1
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- WXMKPNITSTVMEF-UHFFFAOYSA-M sodium benzoate Chemical compound [Na+].[O-]C(=O)C1=CC=CC=C1 WXMKPNITSTVMEF-UHFFFAOYSA-M 0.000 description 1
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- 235000017557 sodium bicarbonate Nutrition 0.000 description 1
- 229910000029 sodium carbonate Inorganic materials 0.000 description 1
- HLBBKKJFGFRGMU-UHFFFAOYSA-M sodium formate Chemical compound [Na+].[O-]C=O HLBBKKJFGFRGMU-UHFFFAOYSA-M 0.000 description 1
- 235000019254 sodium formate Nutrition 0.000 description 1
- RYYKJJJTJZKILX-UHFFFAOYSA-M sodium octadecanoate Chemical compound [Na+].CCCCCCCCCCCCCCCCCC([O-])=O RYYKJJJTJZKILX-UHFFFAOYSA-M 0.000 description 1
- LJFWQNJLLOFIJK-UHFFFAOYSA-N solvent violet 13 Chemical compound C1=CC(C)=CC=C1NC1=CC=C(O)C2=C1C(=O)C1=CC=CC=C1C2=O LJFWQNJLLOFIJK-UHFFFAOYSA-N 0.000 description 1
- 239000001587 sorbitan monostearate Substances 0.000 description 1
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- ISIJQEHRDSCQIU-UHFFFAOYSA-N tert-butyl 2,7-diazaspiro[4.5]decane-7-carboxylate Chemical compound C1N(C(=O)OC(C)(C)C)CCCC11CNCC1 ISIJQEHRDSCQIU-UHFFFAOYSA-N 0.000 description 1
- TUNFSRHWOTWDNC-HKGQFRNVSA-N tetradecanoic acid Chemical compound CCCCCCCCCCCCC[14C](O)=O TUNFSRHWOTWDNC-HKGQFRNVSA-N 0.000 description 1
- 229940073455 tetraethylammonium hydroxide Drugs 0.000 description 1
- LRGJRHZIDJQFCL-UHFFFAOYSA-M tetraethylazanium;hydroxide Chemical compound [OH-].CC[N+](CC)(CC)CC LRGJRHZIDJQFCL-UHFFFAOYSA-M 0.000 description 1
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- STCOOQWBFONSKY-UHFFFAOYSA-N tributyl phosphate Chemical compound CCCCOP(=O)(OCCCC)OCCCC STCOOQWBFONSKY-UHFFFAOYSA-N 0.000 description 1
- GAJQCIFYLSXSEZ-UHFFFAOYSA-L tridecyl phosphate Chemical compound CCCCCCCCCCCCCOP([O-])([O-])=O GAJQCIFYLSXSEZ-UHFFFAOYSA-L 0.000 description 1
- BDZBKCUKTQZUTL-UHFFFAOYSA-N triethyl phosphite Chemical compound CCOP(OCC)OCC BDZBKCUKTQZUTL-UHFFFAOYSA-N 0.000 description 1
- GPHXJBZAVNFMKX-UHFFFAOYSA-M triethyl(phenyl)azanium;hydroxide Chemical compound [OH-].CC[N+](CC)(CC)C1=CC=CC=C1 GPHXJBZAVNFMKX-UHFFFAOYSA-M 0.000 description 1
- ZIBGPFATKBEMQZ-UHFFFAOYSA-N triethylene glycol Chemical compound OCCOCCOCCO ZIBGPFATKBEMQZ-UHFFFAOYSA-N 0.000 description 1
- RXJKFRMDXUJTEX-UHFFFAOYSA-N triethylphosphine Chemical compound CCP(CC)CC RXJKFRMDXUJTEX-UHFFFAOYSA-N 0.000 description 1
- IGNTWNVBGLNYDV-UHFFFAOYSA-N triisopropylphosphine Chemical compound CC(C)P(C(C)C)C(C)C IGNTWNVBGLNYDV-UHFFFAOYSA-N 0.000 description 1
- CYTQBVOFDCPGCX-UHFFFAOYSA-N trimethyl phosphite Chemical compound COP(OC)OC CYTQBVOFDCPGCX-UHFFFAOYSA-N 0.000 description 1
- ZNEOHLHCKGUAEB-UHFFFAOYSA-N trimethylphenylammonium Chemical compound C[N+](C)(C)C1=CC=CC=C1 ZNEOHLHCKGUAEB-UHFFFAOYSA-N 0.000 description 1
- KCTAHLRCZMOTKM-UHFFFAOYSA-N tripropylphosphane Chemical compound CCCP(CCC)CCC KCTAHLRCZMOTKM-UHFFFAOYSA-N 0.000 description 1
- 239000006097 ultraviolet radiation absorber Substances 0.000 description 1
- 238000010792 warming Methods 0.000 description 1
- 238000004383 yellowing Methods 0.000 description 1
- LRXTYHSAJDENHV-UHFFFAOYSA-H zinc phosphate Chemical class [Zn+2].[Zn+2].[Zn+2].[O-]P([O-])([O-])=O.[O-]P([O-])([O-])=O LRXTYHSAJDENHV-UHFFFAOYSA-H 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
- C08G64/20—General preparatory processes
- C08G64/30—General preparatory processes using carbonates
-
- 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
- Y02P20/50—Improvements relating to the production of bulk chemicals
- Y02P20/582—Recycling of unreacted starting or intermediate materials
-
- 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
- Y10—TECHNICAL SUBJECTS COVERED BY FORMER USPC
- Y10T—TECHNICAL SUBJECTS COVERED BY FORMER US CLASSIFICATION
- Y10T428/00—Stock material or miscellaneous articles
- Y10T428/13—Hollow or container type article [e.g., tube, vase, etc.]
- Y10T428/1352—Polymer or resin containing [i.e., natural or synthetic]
Landscapes
- Chemical & Material Sciences (AREA)
- Health & Medical Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Medicinal Chemistry (AREA)
- Polymers & Plastics (AREA)
- Organic Chemistry (AREA)
- Polyesters Or Polycarbonates (AREA)
- Liquid Crystal (AREA)
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| TW201406818A TW201406818A (zh) | 2014-02-16 |
| TWI554546B true TWI554546B (zh) | 2016-10-21 |
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| TW102140657A TWI554546B (zh) | 2007-12-13 | 2008-12-12 | 聚碳酸酯之製造方法 |
| TW097148425A TWI428369B (zh) | 2007-12-13 | 2008-12-12 | 聚碳酸酯之製造方法 |
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| TW097148425A TWI428369B (zh) | 2007-12-13 | 2008-12-12 | 聚碳酸酯之製造方法 |
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| US (1) | US8445624B2 (enExample) |
| EP (3) | EP2952536B1 (enExample) |
| JP (3) | JP4697295B2 (enExample) |
| KR (1) | KR101285525B1 (enExample) |
| CN (3) | CN103992469B (enExample) |
| TW (3) | TWI606080B (enExample) |
| WO (1) | WO2009075305A1 (enExample) |
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| JP5001110B2 (ja) * | 2007-10-04 | 2012-08-15 | 帝人株式会社 | ポリカーボネート樹脂およびその製造方法 |
| CN103992469B (zh) * | 2007-12-13 | 2018-03-16 | 三菱化学株式会社 | 聚碳酸酯及其成型物 |
| CN102224182B (zh) * | 2008-11-28 | 2013-08-07 | 三菱化学株式会社 | 聚碳酸酯树脂、聚碳酸酯树脂组合物、光学膜和聚碳酸酯树脂成型品 |
| EP2789640B1 (en) * | 2008-11-28 | 2019-01-02 | Mitsubishi Chemical Corporation | Polycarbonate resins, polycarbonate resin compositions, optical film, and polycarbonate resin molded articles |
| US8399598B2 (en) * | 2009-04-16 | 2013-03-19 | Teijin Limited | Copolycarbonate and process for producing the same |
| CN102597057A (zh) * | 2009-11-30 | 2012-07-18 | 三菱化学株式会社 | 聚碳酸酯树脂及其制造方法 |
| 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 |
| JP5978554B2 (ja) * | 2009-12-22 | 2016-08-24 | 三菱化学株式会社 | ポリカーボネート樹脂組成物及び成形品 |
| JP5978555B2 (ja) * | 2010-01-07 | 2016-08-24 | 三菱化学株式会社 | ポリカーボネート樹脂組成物及びその成形品 |
| JP5966251B2 (ja) * | 2010-03-26 | 2016-08-10 | 三菱化学株式会社 | ポリカーボネート樹脂組成物及び成形品 |
| JP5502556B2 (ja) * | 2010-03-30 | 2014-05-28 | 大王製紙株式会社 | シリカ複合粒子の製造方法 |
| JP5486377B2 (ja) * | 2010-03-31 | 2014-05-07 | 大王製紙株式会社 | シリカ複合混合無機粒子の製造方法及びシリカ複合混合無機粒子 |
| CN102844353B (zh) | 2010-04-14 | 2016-02-17 | 三菱化学株式会社 | 聚碳酸酯二醇及其制备方法，以及使用了其的聚氨酯和活性能量射线固化性聚合物组合物 |
| EP2558513A1 (en) | 2010-04-14 | 2013-02-20 | Dow Global Technologies LLC | Polycarbonate polyols and polyurethanes made therefrom |
| EP2578616B1 (en) | 2010-05-27 | 2019-12-18 | Mitsubishi Chemical Corporation | Transparent film formed from a polycarbonate resin |
| JP2012067294A (ja) * | 2010-08-25 | 2012-04-05 | Mitsubishi Chemicals Corp | ポリカーボネート樹脂組成物及び成形品 |
| JP2012067287A (ja) * | 2010-08-26 | 2012-04-05 | Mitsubishi Chemicals Corp | 樹脂成形品 |
| JP5786556B2 (ja) * | 2010-08-26 | 2015-09-30 | 三菱化学株式会社 | 樹脂成形品の製造方法 |
| JP6044058B2 (ja) * | 2010-08-31 | 2016-12-14 | 三菱化学株式会社 | ポリカーボネート樹脂組成物及び成形品 |
| CN103314033B (zh) * | 2011-01-07 | 2015-05-27 | 三菱化学株式会社 | 聚碳酸酯的制造方法 |
| CN103380176B (zh) * | 2011-02-16 | 2016-10-26 | 三菱化学株式会社 | 聚碳酸酯树脂组合物和成型品 |
| JP5895581B2 (ja) * | 2011-02-16 | 2016-03-30 | 三菱化学株式会社 | ポリカーボネート樹脂組成物及び成形品 |
| JP5978719B2 (ja) * | 2011-03-30 | 2016-08-24 | 三菱化学株式会社 | ポリカーボネート樹脂の製造方法 |
| WO2012133851A1 (ja) | 2011-03-30 | 2012-10-04 | 三菱化学株式会社 | ポリカーボネート樹脂の製造方法 |
| JP5987406B2 (ja) * | 2011-03-30 | 2016-09-07 | 三菱化学株式会社 | ポリカーボネート樹脂の製造方法 |
| JP5906887B2 (ja) * | 2011-03-30 | 2016-04-20 | 三菱化学株式会社 | ポリカーボネート樹脂の製造方法 |
| JP6015071B2 (ja) * | 2011-03-31 | 2016-10-26 | 三菱化学株式会社 | ポリカーボネートの製造方法および透明フィルム |
| EP2692768B1 (en) * | 2011-03-31 | 2018-01-03 | Mitsubishi Chemical Corporation | Method for producing polycarbonate, and polycarbonate pellets |
| WO2012133856A1 (ja) * | 2011-03-31 | 2012-10-04 | 三菱化学株式会社 | ポリカーボネート樹脂の製造方法、ポリカーボネート樹脂ペレットおよび延伸フィルム |
| CN103476558A (zh) * | 2011-03-31 | 2013-12-25 | 三菱化学株式会社 | 聚碳酸酯树脂的制造方法 |
| WO2012133854A1 (ja) * | 2011-03-31 | 2012-10-04 | 三菱化学株式会社 | ポリカーボネート樹脂の製造方法 |
| WO2012133236A1 (ja) * | 2011-03-31 | 2012-10-04 | 三菱化学株式会社 | ポリカーボネート樹脂の製造方法、ポリカーボネート樹脂、ポリカーボネート樹脂製フィルムおよびポリカーボネート樹脂ペレットの製造方法 |
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| JP2013084584A (ja) * | 2011-09-30 | 2013-05-09 | Mitsubishi Chemicals Corp | Ｌｅｄ照明用部材 |
| JP2013103977A (ja) * | 2011-11-11 | 2013-05-30 | Mitsubishi Rayon Co Ltd | 重合体または重合体溶液の製造方法、重合体、重合体溶液 |
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| JP2013209581A (ja) * | 2012-03-30 | 2013-10-10 | Mitsubishi Chemicals Corp | 成形体 |
| DE102012103296A1 (de) * | 2012-04-17 | 2013-10-17 | List Holding Ag | Verfahren zur Herstellung von Formkörpern |
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| EP2915849B1 (en) * | 2012-11-05 | 2018-03-28 | Idemitsu Kosan Co., Ltd. | Polycarbonate resin composition and molded article |
| JP6154337B2 (ja) * | 2013-02-20 | 2017-06-28 | 帝人株式会社 | ポリカーボネート共重合体 |
| JP2015187204A (ja) * | 2014-03-26 | 2015-10-29 | 三菱化学株式会社 | ポリカーボネート樹脂からなる押出成形品 |
| JP5907232B2 (ja) * | 2014-10-20 | 2016-04-26 | 三菱化学株式会社 | ポリカーボネート樹脂 |
| JP6411882B2 (ja) * | 2014-12-16 | 2018-10-24 | 帝人株式会社 | ポリカーボネート樹脂の製造方法 |
| EP3120924A1 (en) * | 2015-07-24 | 2017-01-25 | Shell Internationale Research Maatschappij B.V. | Apparatus and process for relieving pressure in a chemical plant |
| CN105218802B (zh) * | 2015-10-15 | 2017-05-10 | 宁波浙铁大风化工有限公司 | 一种聚碳酸酯的合成工艺 |
| JP2016027182A (ja) * | 2015-11-16 | 2016-02-18 | 三菱化学株式会社 | ポリカーボネートの製造方法 |
| JP2017165892A (ja) * | 2016-03-17 | 2017-09-21 | 三菱ケミカル株式会社 | 透明樹脂フィルム |
| US10894860B2 (en) * | 2016-03-30 | 2021-01-19 | Mitsubishi Gas Chemical Company, Inc. | High molecular weight aromatic polycarbonate resin manufacturing method |
| CN108699230A (zh) * | 2016-03-30 | 2018-10-23 | 三菱瓦斯化学株式会社 | 高分子量芳香族聚碳酸酯树脂的制造方法 |
| JP6256540B2 (ja) * | 2016-07-08 | 2018-01-10 | 三菱ケミカル株式会社 | リソグラフィー用重合体またはリソグラフィー用重合体溶液の製造方法 |
| CN111630082A (zh) * | 2018-01-24 | 2020-09-04 | Sk化学公司 | 生物基聚碳酸酯及其制备方法 |
| CN111683991B (zh) * | 2018-02-23 | 2022-07-08 | 帝人株式会社 | 聚碳酸酯树脂和制造方法 |
Citations (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JPH10273528A (ja) * | 1997-03-28 | 1998-10-13 | Mitsubishi Chem Corp | 芳香族ポリカーボネートの製造方法 |
| JP2006028441A (ja) * | 2004-07-21 | 2006-02-02 | Teijin Ltd | 脂肪族ポリカーボネートからなる光学用フィルム |
Family Cites Families (30)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| GB1079686A (en) | 1963-05-17 | 1967-08-16 | Courtaulds Ltd | Polyesters |
| JPH0784515B2 (ja) | 1978-10-19 | 1995-09-13 | ビートライス・フーズ・カンパニー | ポリカーボネートの製造方法 |
| JPS5556124A (en) | 1978-10-19 | 1980-04-24 | Beatrice Foods Co | Manufacture of polycarbonate |
| DE2938464A1 (de) * | 1979-09-22 | 1981-04-09 | Bayer Ag, 5090 Leverkusen | Thermoplastische polycarbonate, ihre herstellung und ihre verwendung als formkoerper und folien |
| JPS6312896A (ja) | 1986-07-04 | 1988-01-20 | Hitachi Ltd | ロ−タリコンプレツサの製造方法 |
| JP3197359B2 (ja) * | 1992-08-19 | 2001-08-13 | 日本ジーイープラスチックス株式会社 | 芳香族ポリカーボネートの製造法 |
| DE69607929T2 (de) | 1996-01-30 | 2001-01-18 | Teijin Ltd., Osaka | Polycarbonatcopolymer das Oxaspiroundecangruppe enthält und Verfahren zu seiner Herstellung |
| JP3160209B2 (ja) * | 1996-01-30 | 2001-04-25 | 帝人株式会社 | オキサスピロウンデカン基を含有するポリカーボネート共重合体およびその製造法 |
| JPH10101787A (ja) * | 1996-09-30 | 1998-04-21 | Teijin Ltd | ポリカーボネートおよびその製造方法 |
| JP2989578B2 (ja) * | 1997-04-03 | 1999-12-13 | 旭化成工業株式会社 | 芳香族ポリカーボネートの製法 |
| CA2629496A1 (en) * | 1999-01-11 | 2000-07-20 | E.I. Du Pont De Nemours And Company | Process and products of purification of anhydrosugar alcohols |
| JP3729681B2 (ja) * | 1999-06-11 | 2005-12-21 | 日本ジーイープラスチックス株式会社 | ポリカーボネートの製造方法 |
| JP3685971B2 (ja) * | 2000-01-17 | 2005-08-24 | 三菱化学株式会社 | 芳香族ポリカーボネートの製造方法 |
| JP3694434B2 (ja) * | 2000-02-15 | 2005-09-14 | 三菱化学株式会社 | 芳香族ポリカーボネートの製造方法 |
| FR2810040B1 (fr) * | 2000-06-09 | 2004-04-09 | Roquette Freres | Procede de purification d'une composition contenant au moins un produit de deshydratation interne d'un sucre hydrogene |
| ATE455812T1 (de) | 2003-06-16 | 2010-02-15 | Teijin Ltd | Polycarbonat und herstellungsverfahren dafür |
| CN100432119C (zh) * | 2003-06-16 | 2008-11-12 | 帝人株式会社 | 聚碳酸酯及其制备方法 |
| US7138479B2 (en) * | 2003-12-31 | 2006-11-21 | General Electric Company | Aliphatic diol polycarbonates and their preparation |
| US7132498B2 (en) * | 2004-09-27 | 2006-11-07 | General Electric Company | Process to make polycarbonate from bismethylsalicylcarbonate (BMSC) |
| JP4759518B2 (ja) * | 2004-10-14 | 2011-08-31 | 帝人株式会社 | 光弾性定数の低いポリカーボネート及びそれからなるフィルム |
| JP5170388B2 (ja) * | 2005-07-26 | 2013-03-27 | 宇部興産株式会社 | ポリカーボネート及びその製造方法 |
| JP5032013B2 (ja) * | 2005-09-06 | 2012-09-26 | 帝人株式会社 | 植物由来成分を有するポリカーボネート樹脂組成物 |
| JP2007322490A (ja) | 2006-05-30 | 2007-12-13 | Seiko Epson Corp | 画像形成装置 |
| JP2007322491A (ja) | 2006-05-30 | 2007-12-13 | Seiko Epson Corp | 画像形成装置 |
| JP5532531B2 (ja) * | 2006-06-19 | 2014-06-25 | 三菱化学株式会社 | ポリカーボネート共重合体及びその製造方法 |
| EP2033981B1 (en) * | 2006-06-19 | 2013-08-28 | Mitsubishi Chemical Corporation | Polycarbonate copolymer and method of producing the same |
| WO2008029746A1 (en) | 2006-09-01 | 2008-03-13 | Teijin Limited | Polycarbonate having plant-derived component and method for producing the same |
| JP2008291055A (ja) * | 2007-05-22 | 2008-12-04 | Teijin Ltd | 末端変性ポリカーボネート樹脂組成物 |
| CN102816322A (zh) * | 2007-12-12 | 2012-12-12 | 三菱化学株式会社 | 聚碳酸酯的制造方法和聚碳酸酯成型物 |
| CN103992469B (zh) * | 2007-12-13 | 2018-03-16 | 三菱化学株式会社 | 聚碳酸酯及其成型物 |
-
2008
- 2008-12-10 CN CN201410244465.1A patent/CN103992469B/zh active Active
- 2008-12-10 EP EP15164014.1A patent/EP2952536B1/en active Active
- 2008-12-10 CN CN201410244698.1A patent/CN104017199B/zh active Active
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- 2008-12-10 CN CN200880119869.0A patent/CN101896535B/zh active Active
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-
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- 2011-01-24 JP JP2011012174A patent/JP5857406B2/ja active Active
- 2011-03-24 JP JP2011066586A patent/JP5857425B2/ja active Active
Patent Citations (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JPH10273528A (ja) * | 1997-03-28 | 1998-10-13 | Mitsubishi Chem Corp | 芳香族ポリカーボネートの製造方法 |
| JP2006028441A (ja) * | 2004-07-21 | 2006-02-02 | Teijin Ltd | 脂肪族ポリカーボネートからなる光学用フィルム |
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| EP2952536B1 (en) | 2021-02-24 |
| TW201406818A (zh) | 2014-02-16 |
| EP2952536A3 (en) | 2016-03-23 |
| JP5857406B2 (ja) | 2016-02-10 |
| EP2236540A4 (en) | 2014-10-15 |
| US20110034646A1 (en) | 2011-02-10 |
| JP5857425B2 (ja) | 2016-02-10 |
| CN101896535B (zh) | 2014-07-09 |
| TW200932784A (en) | 2009-08-01 |
| JP2011117008A (ja) | 2011-06-16 |
| CN103992469B (zh) | 2018-03-16 |
| TWI428369B (zh) | 2014-03-01 |
| JP4697295B2 (ja) | 2011-06-08 |
| EP3061782A1 (en) | 2016-08-31 |
| KR20100096133A (ko) | 2010-09-01 |
| US8445624B2 (en) | 2013-05-21 |
| CN103992469A (zh) | 2014-08-20 |
| CN104017199A (zh) | 2014-09-03 |
| TWI606080B (zh) | 2017-11-21 |
| CN101896535A (zh) | 2010-11-24 |
| WO2009075305A1 (ja) | 2009-06-18 |
| EP2952536A2 (en) | 2015-12-09 |
| EP2236540B1 (en) | 2022-03-09 |
| TW201617382A (zh) | 2016-05-16 |
| JP2009161745A (ja) | 2009-07-23 |
| CN104017199B (zh) | 2016-08-31 |
| EP2236540A1 (en) | 2010-10-06 |
| KR101285525B1 (ko) | 2013-07-17 |
| JP2011080091A (ja) | 2011-04-21 |
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