EA011827B1 - Промышленный способ производства диарилкарбоната высокой чистоты - Google Patents
Промышленный способ производства диарилкарбоната высокой чистоты Download PDFInfo
- Publication number
- EA011827B1 EA011827B1 EA200700919A EA200700919A EA011827B1 EA 011827 B1 EA011827 B1 EA 011827B1 EA 200700919 A EA200700919 A EA 200700919A EA 200700919 A EA200700919 A EA 200700919A EA 011827 B1 EA011827 B1 EA 011827B1
- Authority
- EA
- Eurasian Patent Office
- Prior art keywords
- column
- carbonate
- boiling point
- distillation
- reaction
- Prior art date
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- BVKZGUZCCUSVTD-UHFFFAOYSA-L Carbonate Chemical compound [O-]C([O-])=O BVKZGUZCCUSVTD-UHFFFAOYSA-L 0.000 title claims abstract description 56
- 238000000034 method Methods 0.000 title claims description 140
- 238000009835 boiling Methods 0.000 claims abstract description 266
- -1 diaryl carbonate Chemical compound 0.000 claims abstract description 220
- 238000004821 distillation Methods 0.000 claims abstract description 202
- 238000006243 chemical reaction Methods 0.000 claims abstract description 145
- 238000000926 separation method Methods 0.000 claims abstract description 129
- 239000006227 byproduct Substances 0.000 claims abstract description 96
- 125000003118 aryl group Chemical group 0.000 claims abstract description 70
- 239000011541 reaction mixture Substances 0.000 claims abstract description 70
- 150000001875 compounds Chemical class 0.000 claims abstract description 59
- 238000000746 purification Methods 0.000 claims abstract description 57
- 239000007858 starting material Substances 0.000 claims abstract description 50
- 238000005809 transesterification reaction Methods 0.000 claims abstract description 42
- 239000004417 polycarbonate Substances 0.000 claims abstract description 39
- 229920000515 polycarbonate Polymers 0.000 claims abstract description 39
- 238000004519 manufacturing process Methods 0.000 claims abstract description 31
- 239000000463 material Substances 0.000 claims description 125
- 239000000047 product Substances 0.000 claims description 120
- ROORDVPLFPIABK-UHFFFAOYSA-N diphenyl carbonate Chemical compound C=1C=CC=CC=1OC(=O)OC1=CC=CC=C1 ROORDVPLFPIABK-UHFFFAOYSA-N 0.000 claims description 81
- 239000003054 catalyst Substances 0.000 claims description 58
- 239000007788 liquid Substances 0.000 claims description 24
- ZQBAKBUEJOMQEX-UHFFFAOYSA-N phenyl salicylate Chemical compound OC1=CC=CC=C1C(=O)OC1=CC=CC=C1 ZQBAKBUEJOMQEX-UHFFFAOYSA-N 0.000 claims description 19
- 239000002994 raw material Substances 0.000 claims description 19
- 229910052736 halogen Inorganic materials 0.000 claims description 16
- 150000002367 halogens Chemical class 0.000 claims description 16
- 238000010992 reflux Methods 0.000 claims description 15
- 229960000969 phenyl salicylate Drugs 0.000 claims description 10
- 239000002815 homogeneous catalyst Substances 0.000 claims description 7
- 238000009434 installation Methods 0.000 claims description 6
- 229910052799 carbon Inorganic materials 0.000 claims description 5
- GMOYUTKNPLBTMT-UHFFFAOYSA-N 2-phenylmethoxybenzoic acid Chemical compound OC(=O)C1=CC=CC=C1OCC1=CC=CC=C1 GMOYUTKNPLBTMT-UHFFFAOYSA-N 0.000 claims description 4
- 206010028980 Neoplasm Diseases 0.000 claims description 2
- 201000011510 cancer Diseases 0.000 claims description 2
- 238000004140 cleaning Methods 0.000 claims description 2
- 238000007599 discharging Methods 0.000 claims description 2
- JNELGWHKGNBSMD-UHFFFAOYSA-N xanthone Chemical compound C1=CC=C2C(=O)C3=CC=CC=C3OC2=C1 JNELGWHKGNBSMD-UHFFFAOYSA-N 0.000 claims description 2
- 125000001183 hydrocarbyl group Chemical group 0.000 claims 1
- 239000000126 substance Substances 0.000 abstract 2
- 239000000203 mixture Substances 0.000 description 19
- 239000012535 impurity Substances 0.000 description 18
- ISWSIDIOOBJBQZ-UHFFFAOYSA-N Phenol Chemical compound OC1=CC=CC=C1 ISWSIDIOOBJBQZ-UHFFFAOYSA-N 0.000 description 16
- 150000001346 alkyl aryl ethers Chemical class 0.000 description 13
- 150000002430 hydrocarbons Chemical group 0.000 description 13
- 230000007423 decrease Effects 0.000 description 12
- 238000006116 polymerization reaction Methods 0.000 description 11
- RDOXTESZEPMUJZ-UHFFFAOYSA-N anisole Chemical compound COC1=CC=CC=C1 RDOXTESZEPMUJZ-UHFFFAOYSA-N 0.000 description 10
- 239000007789 gas Substances 0.000 description 9
- 238000012360 testing method Methods 0.000 description 9
- 150000004945 aromatic hydrocarbons Chemical class 0.000 description 8
- 150000004649 carbonic acid derivatives Chemical class 0.000 description 8
- IEJIGPNLZYLLBP-UHFFFAOYSA-N dimethyl carbonate Chemical compound COC(=O)OC IEJIGPNLZYLLBP-UHFFFAOYSA-N 0.000 description 8
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 7
- XTBFPVLHGVYOQH-UHFFFAOYSA-N methyl phenyl carbonate Chemical compound COC(=O)OC1=CC=CC=C1 XTBFPVLHGVYOQH-UHFFFAOYSA-N 0.000 description 7
- 150000002989 phenols Chemical class 0.000 description 7
- 238000004064 recycling Methods 0.000 description 7
- 238000007086 side reaction Methods 0.000 description 7
- OKKJLVBELUTLKV-UHFFFAOYSA-N Methanol Chemical compound OC OKKJLVBELUTLKV-UHFFFAOYSA-N 0.000 description 6
- 125000000217 alkyl group Chemical group 0.000 description 6
- 125000005161 aryl oxy carbonyl group Chemical group 0.000 description 6
- 125000004432 carbon atom Chemical group C* 0.000 description 6
- 230000007774 longterm Effects 0.000 description 6
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 6
- 230000015572 biosynthetic process Effects 0.000 description 5
- 230000003197 catalytic effect Effects 0.000 description 5
- UZKWTJUDCOPSNM-UHFFFAOYSA-N methoxybenzene Substances CCCCOC=C UZKWTJUDCOPSNM-UHFFFAOYSA-N 0.000 description 5
- YGYAWVDWMABLBF-UHFFFAOYSA-N Phosgene Chemical compound ClC(Cl)=O YGYAWVDWMABLBF-UHFFFAOYSA-N 0.000 description 4
- 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 4
- 239000012295 chemical reaction liquid Substances 0.000 description 4
- 238000007323 disproportionation reaction Methods 0.000 description 4
- PFYHAAAQPNMZHO-UHFFFAOYSA-N methoxy-benzoic acid methyl ester Natural products COC(=O)C1=CC=CC=C1OC PFYHAAAQPNMZHO-UHFFFAOYSA-N 0.000 description 4
- GSNDBZWPIPOOKL-UHFFFAOYSA-N 2-methoxyethyl phenyl carbonate Chemical compound COCCOC(=O)OC1=CC=CC=C1 GSNDBZWPIPOOKL-UHFFFAOYSA-N 0.000 description 3
- 241001120493 Arene Species 0.000 description 3
- 125000002723 alicyclic group Chemical group 0.000 description 3
- 125000003545 alkoxy group Chemical group 0.000 description 3
- 125000004453 alkoxycarbonyl group Chemical group 0.000 description 3
- 125000003710 aryl alkyl group Chemical group 0.000 description 3
- 230000006866 deterioration Effects 0.000 description 3
- 230000003628 erosive effect Effects 0.000 description 3
- 238000001704 evaporation Methods 0.000 description 3
- 230000008020 evaporation Effects 0.000 description 3
- 239000012530 fluid Substances 0.000 description 3
- 125000005843 halogen group Chemical group 0.000 description 3
- 125000004356 hydroxy functional group Chemical group O* 0.000 description 3
- 238000009776 industrial production Methods 0.000 description 3
- 238000001746 injection moulding Methods 0.000 description 3
- 229910052751 metal Inorganic materials 0.000 description 3
- 239000002184 metal Substances 0.000 description 3
- 230000035484 reaction time Effects 0.000 description 3
- GJYCVCVHRSWLNY-UHFFFAOYSA-N 2-butylphenol Chemical compound CCCCC1=CC=CC=C1O GJYCVCVHRSWLNY-UHFFFAOYSA-N 0.000 description 2
- QTWJRLJHJPIABL-UHFFFAOYSA-N 2-methylphenol;3-methylphenol;4-methylphenol Chemical compound CC1=CC=C(O)C=C1.CC1=CC=CC(O)=C1.CC1=CC=CC=C1O QTWJRLJHJPIABL-UHFFFAOYSA-N 0.000 description 2
- MJKVTPMWOKAVMS-UHFFFAOYSA-N 3-hydroxy-1-benzopyran-2-one Chemical compound C1=CC=C2OC(=O)C(O)=CC2=C1 MJKVTPMWOKAVMS-UHFFFAOYSA-N 0.000 description 2
- 239000004215 Carbon black (E152) Substances 0.000 description 2
- ZAMOUSCENKQFHK-UHFFFAOYSA-N Chlorine atom Chemical compound [Cl] ZAMOUSCENKQFHK-UHFFFAOYSA-N 0.000 description 2
- RTZKZFJDLAIYFH-UHFFFAOYSA-N Diethyl ether Chemical compound CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 description 2
- 125000002877 alkyl aryl group Chemical group 0.000 description 2
- 125000004104 aryloxy group Chemical group 0.000 description 2
- 150000001720 carbohydrates Chemical class 0.000 description 2
- 239000007795 chemical reaction product Substances 0.000 description 2
- 229910052801 chlorine Inorganic materials 0.000 description 2
- 239000000460 chlorine Substances 0.000 description 2
- 230000000052 comparative effect Effects 0.000 description 2
- 229930003836 cresol Natural products 0.000 description 2
- 238000011161 development Methods 0.000 description 2
- 230000018109 developmental process Effects 0.000 description 2
- 230000000694 effects Effects 0.000 description 2
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- 238000002347 injection Methods 0.000 description 2
- 239000007924 injection Substances 0.000 description 2
- 238000004255 ion exchange chromatography Methods 0.000 description 2
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 description 2
- OSWPMRLSEDHDFF-UHFFFAOYSA-N methyl salicylate Chemical compound COC(=O)C1=CC=CC=C1O OSWPMRLSEDHDFF-UHFFFAOYSA-N 0.000 description 2
- IXQGCWUGDFDQMF-UHFFFAOYSA-N o-Hydroxyethylbenzene Natural products CCC1=CC=CC=C1O IXQGCWUGDFDQMF-UHFFFAOYSA-N 0.000 description 2
- 238000012856 packing Methods 0.000 description 2
- 239000004033 plastic Substances 0.000 description 2
- 229920003023 plastic Polymers 0.000 description 2
- 238000000066 reactive distillation Methods 0.000 description 2
- 239000010935 stainless steel Substances 0.000 description 2
- 229910001220 stainless steel Inorganic materials 0.000 description 2
- 125000001424 substituent group Chemical group 0.000 description 2
- 238000005406 washing Methods 0.000 description 2
- KJCVRFUGPWSIIH-UHFFFAOYSA-N 1-naphthol Chemical compound C1=CC=C2C(O)=CC=CC2=C1 KJCVRFUGPWSIIH-UHFFFAOYSA-N 0.000 description 1
- PXSSNPBEHHJLDH-UHFFFAOYSA-N 2,3,4,5-tetramethylphenol Chemical compound CC1=CC(O)=C(C)C(C)=C1C PXSSNPBEHHJLDH-UHFFFAOYSA-N 0.000 description 1
- XRUGBBIQLIVCSI-UHFFFAOYSA-N 2,3,4-trimethylphenol Chemical compound CC1=CC=C(O)C(C)=C1C XRUGBBIQLIVCSI-UHFFFAOYSA-N 0.000 description 1
- RLEWTHFVGOXXTN-UHFFFAOYSA-N 2,3-diethylphenol Chemical compound CCC1=CC=CC(O)=C1CC RLEWTHFVGOXXTN-UHFFFAOYSA-N 0.000 description 1
- HRQPPTDGMMGDKC-UHFFFAOYSA-N 2,3-dipropylphenol Chemical compound CCCC1=CC=CC(O)=C1CCC HRQPPTDGMMGDKC-UHFFFAOYSA-N 0.000 description 1
- JSGXYACZKHCRTI-UHFFFAOYSA-N 2-(3-phenylpropyl)phenol Chemical compound OC1=CC=CC=C1CCCC1=CC=CC=C1 JSGXYACZKHCRTI-UHFFFAOYSA-N 0.000 description 1
- ASLNDVUAZOHADR-UHFFFAOYSA-N 2-butyl-3-methylphenol Chemical compound CCCCC1=C(C)C=CC=C1O ASLNDVUAZOHADR-UHFFFAOYSA-N 0.000 description 1
- 125000001731 2-cyanoethyl group Chemical group [H]C([H])(*)C([H])([H])C#N 0.000 description 1
- MVRPPTGLVPEMPI-UHFFFAOYSA-N 2-cyclohexylphenol Chemical compound OC1=CC=CC=C1C1CCCCC1 MVRPPTGLVPEMPI-UHFFFAOYSA-N 0.000 description 1
- MOEFFSWKSMRFRQ-UHFFFAOYSA-N 2-ethoxyphenol Chemical compound CCOC1=CC=CC=C1O MOEFFSWKSMRFRQ-UHFFFAOYSA-N 0.000 description 1
- ABMULKFGWTYIIK-UHFFFAOYSA-N 2-hexylphenol Chemical compound CCCCCCC1=CC=CC=C1O ABMULKFGWTYIIK-UHFFFAOYSA-N 0.000 description 1
- MEEKGULDSDXFCN-UHFFFAOYSA-N 2-pentylphenol Chemical compound CCCCCC1=CC=CC=C1O MEEKGULDSDXFCN-UHFFFAOYSA-N 0.000 description 1
- 125000000094 2-phenylethyl group Chemical group [H]C1=C([H])C([H])=C(C([H])=C1[H])C([H])([H])C([H])([H])* 0.000 description 1
- 125000003903 2-propenyl group Chemical group [H]C([*])([H])C([H])=C([H])[H] 0.000 description 1
- LCHYEKKJCUJAKN-UHFFFAOYSA-N 2-propylphenol Chemical compound CCCC1=CC=CC=C1O LCHYEKKJCUJAKN-UHFFFAOYSA-N 0.000 description 1
- FCUBUGPGVCEURB-UHFFFAOYSA-N 3-methyl-2-propylphenol Chemical compound CCCC1=C(C)C=CC=C1O FCUBUGPGVCEURB-UHFFFAOYSA-N 0.000 description 1
- GJCOSYZMQJWQCA-UHFFFAOYSA-N 9H-xanthene Chemical compound C1=CC=C2CC3=CC=CC=C3OC2=C1 GJCOSYZMQJWQCA-UHFFFAOYSA-N 0.000 description 1
- 229910000975 Carbon steel Inorganic materials 0.000 description 1
- OIFBSDVPJOWBCH-UHFFFAOYSA-N Diethyl carbonate Chemical compound CCOC(=O)OCC OIFBSDVPJOWBCH-UHFFFAOYSA-N 0.000 description 1
- KMTRUDSVKNLOMY-UHFFFAOYSA-N Ethylene carbonate Chemical compound O=C1OCCO1 KMTRUDSVKNLOMY-UHFFFAOYSA-N 0.000 description 1
- 241001602876 Nata Species 0.000 description 1
- CTQNGGLPUBDAKN-UHFFFAOYSA-N O-Xylene Chemical compound CC1=CC=CC=C1C CTQNGGLPUBDAKN-UHFFFAOYSA-N 0.000 description 1
- RTAQQCXQSZGOHL-UHFFFAOYSA-N Titanium Chemical compound [Ti] RTAQQCXQSZGOHL-UHFFFAOYSA-N 0.000 description 1
- 239000013543 active substance Substances 0.000 description 1
- 150000001298 alcohols Chemical class 0.000 description 1
- 239000012670 alkaline solution Substances 0.000 description 1
- 125000004848 alkoxyethyl group Chemical group 0.000 description 1
- 125000005910 alkyl carbonate group Chemical group 0.000 description 1
- 238000000998 batch distillation Methods 0.000 description 1
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- 230000009286 beneficial effect Effects 0.000 description 1
- 125000001797 benzyl group Chemical group [H]C1=C([H])C([H])=C(C([H])=C1[H])C([H])([H])* 0.000 description 1
- 239000004305 biphenyl Substances 0.000 description 1
- 235000010290 biphenyl Nutrition 0.000 description 1
- WQULVXNWEYLDJY-UHFFFAOYSA-N bis(2-chloroethyl) carbonate Chemical compound ClCCOC(=O)OCCCl WQULVXNWEYLDJY-UHFFFAOYSA-N 0.000 description 1
- STLGQBDVSTWGIP-UHFFFAOYSA-N bis(2-methoxyethyl) carbonate Chemical compound COCCOC(=O)OCCOC STLGQBDVSTWGIP-UHFFFAOYSA-N 0.000 description 1
- IHYIGUIPVVUALV-UHFFFAOYSA-N bis(3-phenylpropyl) carbonate Chemical compound C=1C=CC=CC=1CCCOC(=O)OCCCC1=CC=CC=C1 IHYIGUIPVVUALV-UHFFFAOYSA-N 0.000 description 1
- BUEBPZHICJLZNL-UHFFFAOYSA-N bis(methoxymethyl) carbonate Chemical compound COCOC(=O)OCOC BUEBPZHICJLZNL-UHFFFAOYSA-N 0.000 description 1
- JKJWYKGYGWOAHT-UHFFFAOYSA-N bis(prop-2-enyl) carbonate Chemical compound C=CCOC(=O)OCC=C JKJWYKGYGWOAHT-UHFFFAOYSA-N 0.000 description 1
- HXXOUQFXWDBCTO-UHFFFAOYSA-N bis[chloro(phenyl)methyl] carbonate Chemical compound C=1C=CC=CC=1C(Cl)OC(=O)OC(Cl)C1=CC=CC=C1 HXXOUQFXWDBCTO-UHFFFAOYSA-N 0.000 description 1
- AGAJWGOEYSXAFN-UHFFFAOYSA-N bis[methoxy(phenyl)methyl] carbonate Chemical compound C=1C=CC=CC=1C(OC)OC(=O)OC(OC)C1=CC=CC=C1 AGAJWGOEYSXAFN-UHFFFAOYSA-N 0.000 description 1
- 125000004369 butenyl group Chemical group C(=CCC)* 0.000 description 1
- 125000000484 butyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 description 1
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- 229910052802 copper Inorganic materials 0.000 description 1
- 230000007797 corrosion Effects 0.000 description 1
- 238000005260 corrosion Methods 0.000 description 1
- 125000000853 cresyl group Chemical group C1(=CC=C(C=C1)C)* 0.000 description 1
- 238000002425 crystallisation Methods 0.000 description 1
- 125000004093 cyano group Chemical group *C#N 0.000 description 1
- 125000001995 cyclobutyl group Chemical group [H]C1([H])C([H])([H])C([H])(*)C1([H])[H] 0.000 description 1
- 125000000582 cycloheptyl group Chemical group [H]C1([H])C([H])([H])C([H])([H])C([H])([H])C([H])(*)C([H])([H])C1([H])[H] 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
- 125000004210 cyclohexylmethyl group Chemical group [H]C([H])(*)C1([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C1([H])[H] 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
- 125000001559 cyclopropyl group Chemical group [H]C1([H])C([H])([H])C1([H])* 0.000 description 1
- 125000002704 decyl 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])* 0.000 description 1
- 238000013461 design Methods 0.000 description 1
- PIZLBWGMERQCOC-UHFFFAOYSA-N dibenzyl carbonate Chemical compound C=1C=CC=CC=1COC(=O)OCC1=CC=CC=C1 PIZLBWGMERQCOC-UHFFFAOYSA-N 0.000 description 1
- QLVWOKQMDLQXNN-UHFFFAOYSA-N dibutyl carbonate Chemical compound CCCCOC(=O)OCCCC QLVWOKQMDLQXNN-UHFFFAOYSA-N 0.000 description 1
- ZKPAPYUSLATAMS-UHFFFAOYSA-N dicycloheptyl carbonate Chemical compound C1CCCCCC1OC(=O)OC1CCCCCC1 ZKPAPYUSLATAMS-UHFFFAOYSA-N 0.000 description 1
- FYIBPWZEZWVDQB-UHFFFAOYSA-N dicyclohexyl carbonate Chemical compound C1CCCCC1OC(=O)OC1CCCCC1 FYIBPWZEZWVDQB-UHFFFAOYSA-N 0.000 description 1
- AJHQRWJZHVBYLU-UHFFFAOYSA-N dicyclopentyl carbonate Chemical compound C1CCCC1OC(=O)OC1CCCC1 AJHQRWJZHVBYLU-UHFFFAOYSA-N 0.000 description 1
- ZEBJPYUECLCDRQ-UHFFFAOYSA-N didecyl carbonate Chemical compound CCCCCCCCCCOC(=O)OCCCCCCCCCC ZEBJPYUECLCDRQ-UHFFFAOYSA-N 0.000 description 1
- FHWFURWDUGYUMA-UHFFFAOYSA-N dinonyl carbonate Chemical compound CCCCCCCCCOC(=O)OCCCCCCCCC FHWFURWDUGYUMA-UHFFFAOYSA-N 0.000 description 1
- VUPKGFBOKBGHFZ-UHFFFAOYSA-N dipropyl carbonate Chemical compound CCCOC(=O)OCCC VUPKGFBOKBGHFZ-UHFFFAOYSA-N 0.000 description 1
- 238000002845 discoloration Methods 0.000 description 1
- 238000004090 dissolution Methods 0.000 description 1
- 125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 description 1
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- 238000000227 grinding Methods 0.000 description 1
- LHGVFZTZFXWLCP-UHFFFAOYSA-N guaiacol Chemical compound COC1=CC=CC=C1O LHGVFZTZFXWLCP-UHFFFAOYSA-N 0.000 description 1
- 125000003187 heptyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 description 1
- 125000001072 heteroaryl group Chemical group 0.000 description 1
- 125000004051 hexyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])* 0.000 description 1
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- PUGYLBSXMKBSRP-UHFFFAOYSA-N methyl 2-phenoxybenzoate Chemical compound COC(=O)C1=CC=CC=C1OC1=CC=CC=C1 PUGYLBSXMKBSRP-UHFFFAOYSA-N 0.000 description 1
- 125000006178 methyl benzyl group Chemical group 0.000 description 1
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- 125000001400 nonyl group Chemical group [H]C([*])([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])[H] 0.000 description 1
- 125000002347 octyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 description 1
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- ZUOUZKKEUPVFJK-UHFFFAOYSA-N phenylbenzene Natural products C1=CC=CC=C1C1=CC=CC=C1 ZUOUZKKEUPVFJK-UHFFFAOYSA-N 0.000 description 1
- 125000004344 phenylpropyl group Chemical group 0.000 description 1
- RGCLLPNLLBQHPF-HJWRWDBZSA-N phosphamidon Chemical compound CCN(CC)C(=O)C(\Cl)=C(/C)OP(=O)(OC)OC RGCLLPNLLBQHPF-HJWRWDBZSA-N 0.000 description 1
- 230000002035 prolonged effect Effects 0.000 description 1
- 125000001436 propyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])[H] 0.000 description 1
- 108090000623 proteins and genes Proteins 0.000 description 1
- UBQKCCHYAOITMY-UHFFFAOYSA-N pyridin-2-ol Chemical compound OC1=CC=CC=N1 UBQKCCHYAOITMY-UHFFFAOYSA-N 0.000 description 1
- MCJGNVYPOGVAJF-UHFFFAOYSA-N quinolin-8-ol Chemical compound C1=CN=C2C(O)=CC=CC2=C1 MCJGNVYPOGVAJF-UHFFFAOYSA-N 0.000 description 1
- 230000008707 rearrangement Effects 0.000 description 1
- 238000011160 research Methods 0.000 description 1
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- URGAHOPLAPQHLN-UHFFFAOYSA-N sodium aluminosilicate Chemical compound [Na+].[Al+3].[O-][Si]([O-])=O.[O-][Si]([O-])=O URGAHOPLAPQHLN-UHFFFAOYSA-N 0.000 description 1
- 238000001179 sorption measurement Methods 0.000 description 1
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- 238000013519 translation Methods 0.000 description 1
- 229920001285 xanthan gum Polymers 0.000 description 1
- 150000007964 xanthones Chemical class 0.000 description 1
- 239000008096 xylene Substances 0.000 description 1
Classifications
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B01—PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
- B01D—SEPARATION
- B01D3/00—Distillation or related exchange processes in which liquids are contacted with gaseous media, e.g. stripping
- B01D3/14—Fractional distillation or use of a fractionation or rectification column
- B01D3/143—Fractional distillation or use of a fractionation or rectification column by two or more of a fractionation, separation or rectification step
- B01D3/146—Multiple effect distillation
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C68/00—Preparation of esters of carbonic or haloformic acids
- C07C68/08—Purification; Separation; Stabilisation
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B01—PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
- B01D—SEPARATION
- B01D3/00—Distillation or related exchange processes in which liquids are contacted with gaseous media, e.g. stripping
- B01D3/009—Distillation or related exchange processes in which liquids are contacted with gaseous media, e.g. stripping in combination with chemical reactions
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B01—PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
- B01D—SEPARATION
- B01D3/00—Distillation or related exchange processes in which liquids are contacted with gaseous media, e.g. stripping
- B01D3/14—Fractional distillation or use of a fractionation or rectification column
- B01D3/16—Fractionating columns in which vapour bubbles through liquid
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B01—PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
- B01D—SEPARATION
- B01D3/00—Distillation or related exchange processes in which liquids are contacted with gaseous media, e.g. stripping
- B01D3/14—Fractional distillation or use of a fractionation or rectification column
- B01D3/16—Fractionating columns in which vapour bubbles through liquid
- B01D3/22—Fractionating columns in which vapour bubbles through liquid with horizontal sieve plates or grids; Construction of sieve plates or grids
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C68/00—Preparation of esters of carbonic or haloformic acids
- C07C68/06—Preparation of esters of carbonic or haloformic acids from organic carbonates
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C68/00—Preparation of esters of carbonic or haloformic acids
- C07C68/06—Preparation of esters of carbonic or haloformic acids from organic carbonates
- C07C68/065—Preparation of esters of carbonic or haloformic acids from organic carbonates from alkylene carbonates
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C69/00—Esters of carboxylic acids; Esters of carbonic or haloformic acids
- C07C69/96—Esters of carbonic or haloformic acids
-
- 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
- C08G64/307—General preparatory processes using carbonates and phenols
-
- 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
- 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
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Health & Medical Sciences (AREA)
- Medicinal Chemistry (AREA)
- Polymers & Plastics (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
- Vaporization, Distillation, Condensation, Sublimation, And Cold Traps (AREA)
- Low-Molecular Organic Synthesis Reactions Using Catalysts (AREA)
Applications Claiming Priority (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP2004308127 | 2004-10-22 | ||
| PCT/JP2005/019001 WO2006043491A1 (ja) | 2004-10-22 | 2005-10-17 | 高純度ジアリールカーボネートの工業的製造方法 |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| EA200700919A1 EA200700919A1 (ru) | 2008-02-28 |
| EA011827B1 true EA011827B1 (ru) | 2009-06-30 |
Family
ID=36202907
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| EA200700919A EA011827B1 (ru) | 2004-10-22 | 2005-10-17 | Промышленный способ производства диарилкарбоната высокой чистоты |
Country Status (9)
| Country | Link |
|---|---|
| US (1) | US20070260084A1 (OSRAM) |
| EP (1) | EP1803704A1 (OSRAM) |
| JP (1) | JP4224514B2 (OSRAM) |
| KR (2) | KR20080104197A (OSRAM) |
| CN (1) | CN101044109B (OSRAM) |
| BR (1) | BRPI0515032A (OSRAM) |
| EA (1) | EA011827B1 (OSRAM) |
| IN (1) | IN2007KN01112A (OSRAM) |
| WO (1) | WO2006043491A1 (OSRAM) |
Families Citing this family (15)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| WO2006001257A1 (ja) * | 2004-06-25 | 2006-01-05 | Asahi Kasei Chemicals Corporation | 芳香族カーボネートの工業的製造方法 |
| JP4224510B2 (ja) * | 2004-07-13 | 2009-02-18 | 旭化成ケミカルズ株式会社 | 芳香族カーボネート類の工業的製造法 |
| JP4292210B2 (ja) | 2004-08-25 | 2009-07-08 | 旭化成ケミカルズ株式会社 | 高純度ジフェニルカーボネートの工業的製造方法 |
| BRPI0514693A (pt) * | 2004-09-03 | 2008-06-17 | Asahi Kasei Chemicals Corp | aperfeiçoamento em um processo industrial para a produção de carbonato de diarila de pureza elevada, carbonato de difenila de pureza elevada, e, aparelho para produzir o mesmo |
| US7622601B2 (en) | 2004-10-14 | 2009-11-24 | Asahi Kasei Chemicals Corporation | Process for production of high-purity diaryl carbonate |
| EP1961781A4 (en) * | 2005-12-12 | 2010-04-28 | Asahi Kasei Chemicals Corp | METHOD FOR THE INDUSTRIAL MANUFACTURE OF HIGHLY QUALITATIVE, AROMATIC POLYCARBONATE |
| IN2014DN07638A (OSRAM) * | 2007-02-16 | 2015-07-10 | Sabic Innovative Plastics Ip | |
| CN101605750B (zh) * | 2007-02-16 | 2013-05-08 | 沙伯基础创新塑料知识产权有限公司 | 碳酸二甲酯的制备方法 |
| KR101047928B1 (ko) | 2007-05-08 | 2011-07-08 | 주식회사 엘지화학 | 저비점, 중비점 및 고비점 물질을 포함하는 원료의 분리방법 |
| DE102007055266A1 (de) * | 2007-11-20 | 2009-05-28 | Bayer Materialscience Ag | Verfahren zur Reinigung von Diarylcarbonaten |
| US8907116B2 (en) * | 2009-08-12 | 2014-12-09 | Shell Oil Company | Process for removing an alkanol impurity from a dialkyl carbonate stream |
| EP2703423B1 (en) * | 2011-06-29 | 2017-09-06 | SABIC Global Technologies B.V. | Late-addition catalyst formulation |
| CN109096115A (zh) * | 2018-07-02 | 2018-12-28 | 赵杰 | 一种碳酸甲乙酯制备工艺 |
| CN113233982B (zh) * | 2021-04-30 | 2022-12-09 | 上海化工研究院有限公司 | 一种连续精馏提纯获得高纯度水杨酸甲酯的装置及方法 |
| EP4414357A4 (en) | 2021-10-05 | 2025-01-22 | Asahi Kasei Kabushiki Kaisha | PROCESS FOR THE PRODUCTION OF HIGH PURITY DIARYL CARBONATE |
Citations (5)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JPH04100824A (ja) * | 1990-08-21 | 1992-04-02 | Asahi Chem Ind Co Ltd | 芳香族ポリカーボネートの製法 |
| JPH09110805A (ja) * | 1995-10-17 | 1997-04-28 | Mitsubishi Chem Corp | ジアリールカーボネート製造方法 |
| JP2001064235A (ja) * | 1999-08-27 | 2001-03-13 | Chiyoda Corp | ジアリールカーボネートの製造方法 |
| JP2003516376A (ja) * | 1999-12-08 | 2003-05-13 | ゼネラル・エレクトリック・カンパニイ | ジアリールカーボネートの連続生産法及び装置 |
| JP2004323384A (ja) * | 2003-04-22 | 2004-11-18 | Mitsubishi Gas Chem Co Inc | ジアリールカーボネートの連続的製造方法 |
Family Cites Families (12)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US4182726A (en) * | 1974-06-25 | 1980-01-08 | Snamprogetti, S.P.A. | Process for the preparation of aromatic carbonates |
| DE69117174T2 (de) * | 1990-11-29 | 1996-07-04 | Nitto Denko Corp | Filtrationsfilm für flüssigkeiten sowie diesen film verwendende filtervorrichtung |
| DE4218061A1 (de) * | 1992-06-01 | 1993-12-02 | Bayer Ag | Verfahren zur Herstellung von organischen Carbonaten mit mindestens einer aromatischen Estergruppe |
| DE4226756A1 (de) * | 1992-08-13 | 1994-02-17 | Bayer Ag | Verfahren zur Herstellung von Dicarbonaten |
| DE4226755A1 (de) * | 1992-08-13 | 1994-02-17 | Bayer Ag | Verfahren zur kontinuierlichen Herstellung von Diarylcarbonaten aus Dialkylcarbonaten |
| ES2174126T3 (es) | 1995-12-22 | 2002-11-01 | Asahi Chemical Ind | Metodo para la produccion en continuo de dialquil carbonato y dioles. |
| IT1282363B1 (it) * | 1996-01-16 | 1998-03-20 | Enichem Spa | Procedimento continuo per la preparazione di fenil metil carbonato |
| TW442516B (en) * | 1996-01-17 | 2001-06-23 | Asahi Chemical Ind | Method for producing an aromatic polycarbonate having improved melt stability |
| JP4112048B2 (ja) * | 1997-09-16 | 2008-07-02 | 旭化成ケミカルズ株式会社 | 芳香族カーボネート類の製法 |
| US5990362A (en) * | 1998-08-31 | 1999-11-23 | General Electric Company | Method for preparing bisphenol A |
| US6600061B1 (en) * | 2000-11-15 | 2003-07-29 | General Electric Company | Method for the continuous production of aromatic carbonates |
| CN1280331C (zh) * | 2000-12-07 | 2006-10-18 | 伊斯曼化学公司 | 使用管式反应器的聚酯工艺 |
-
2005
- 2005-10-17 BR BRPI0515032-9A patent/BRPI0515032A/pt not_active IP Right Cessation
- 2005-10-17 EP EP05793362A patent/EP1803704A1/en not_active Withdrawn
- 2005-10-17 WO PCT/JP2005/019001 patent/WO2006043491A1/ja not_active Ceased
- 2005-10-17 KR KR1020087025325A patent/KR20080104197A/ko not_active Abandoned
- 2005-10-17 KR KR1020077005297A patent/KR100887915B1/ko not_active Expired - Fee Related
- 2005-10-17 JP JP2006542956A patent/JP4224514B2/ja not_active Expired - Lifetime
- 2005-10-17 IN IN1112KON2007 patent/IN2007KN01112A/en unknown
- 2005-10-17 US US11/661,611 patent/US20070260084A1/en not_active Abandoned
- 2005-10-17 EA EA200700919A patent/EA011827B1/ru not_active IP Right Cessation
- 2005-10-17 CN CN2005800355135A patent/CN101044109B/zh not_active Expired - Lifetime
Patent Citations (5)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JPH04100824A (ja) * | 1990-08-21 | 1992-04-02 | Asahi Chem Ind Co Ltd | 芳香族ポリカーボネートの製法 |
| JPH09110805A (ja) * | 1995-10-17 | 1997-04-28 | Mitsubishi Chem Corp | ジアリールカーボネート製造方法 |
| JP2001064235A (ja) * | 1999-08-27 | 2001-03-13 | Chiyoda Corp | ジアリールカーボネートの製造方法 |
| JP2003516376A (ja) * | 1999-12-08 | 2003-05-13 | ゼネラル・エレクトリック・カンパニイ | ジアリールカーボネートの連続生産法及び装置 |
| JP2004323384A (ja) * | 2003-04-22 | 2004-11-18 | Mitsubishi Gas Chem Co Inc | ジアリールカーボネートの連続的製造方法 |
Also Published As
| Publication number | Publication date |
|---|---|
| KR20080104197A (ko) | 2008-12-01 |
| KR20070039983A (ko) | 2007-04-13 |
| KR100887915B1 (ko) | 2009-03-12 |
| EP1803704A1 (en) | 2007-07-04 |
| WO2006043491A1 (ja) | 2006-04-27 |
| IN2007KN01112A (OSRAM) | 2007-07-13 |
| JP4224514B2 (ja) | 2009-02-18 |
| CN101044109B (zh) | 2011-07-06 |
| CN101044109A (zh) | 2007-09-26 |
| JPWO2006043491A1 (ja) | 2008-05-22 |
| BRPI0515032A (pt) | 2008-07-01 |
| US20070260084A1 (en) | 2007-11-08 |
| EA200700919A1 (ru) | 2008-02-28 |
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Legal Events
| Date | Code | Title | Description |
|---|---|---|---|
| MM4A | Lapse of a eurasian patent due to non-payment of renewal fees within the time limit in the following designated state(s) |
Designated state(s): AM AZ BY KZ KG MD TJ TM RU |