JP2006511667A5 - - Google Patents
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- Publication number
- JP2006511667A5 JP2006511667A5 JP2004565308A JP2004565308A JP2006511667A5 JP 2006511667 A5 JP2006511667 A5 JP 2006511667A5 JP 2004565308 A JP2004565308 A JP 2004565308A JP 2004565308 A JP2004565308 A JP 2004565308A JP 2006511667 A5 JP2006511667 A5 JP 2006511667A5
- Authority
- JP
- Japan
- Prior art keywords
- acetate
- tetrapropylphosphonium
- tetramethylphosphonium
- tetraethylphosphonium
- molecular weight
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Withdrawn
Links
- 229920000515 polycarbonate Polymers 0.000 claims 13
- 239000004417 polycarbonate Substances 0.000 claims 13
- HEMHJVSKTPXQMS-UHFFFAOYSA-M Sodium hydroxide Chemical group [OH-].[Na+] HEMHJVSKTPXQMS-UHFFFAOYSA-M 0.000 claims 12
- 238000000034 method Methods 0.000 claims 10
- BVKZGUZCCUSVTD-UHFFFAOYSA-L Carbonate Chemical compound [O-]C([O-])=O BVKZGUZCCUSVTD-UHFFFAOYSA-L 0.000 claims 7
- ISWSIDIOOBJBQZ-UHFFFAOYSA-N Phenol Chemical compound OC1=CC=CC=C1 ISWSIDIOOBJBQZ-UHFFFAOYSA-N 0.000 claims 7
- 150000001875 compounds Chemical class 0.000 claims 7
- IISBACLAFKSPIT-UHFFFAOYSA-N bisphenol A Chemical compound C=1C=C(O)C=CC=1C(C)(C)C1=CC=C(O)C=C1 IISBACLAFKSPIT-UHFFFAOYSA-N 0.000 claims 6
- 239000002243 precursor Substances 0.000 claims 6
- 239000003960 organic solvent Substances 0.000 claims 5
- LYCAIKOWRPUZTN-UHFFFAOYSA-N Ethylene glycol Chemical compound OCCO LYCAIKOWRPUZTN-UHFFFAOYSA-N 0.000 claims 3
- KWYUFKZDYYNOTN-UHFFFAOYSA-M Potassium hydroxide Chemical compound [OH-].[K+] KWYUFKZDYYNOTN-UHFFFAOYSA-M 0.000 claims 3
- ZMANZCXQSJIPKH-UHFFFAOYSA-N Triethylamine Chemical compound CCN(CC)CC ZMANZCXQSJIPKH-UHFFFAOYSA-N 0.000 claims 3
- 238000009835 boiling Methods 0.000 claims 3
- 239000003054 catalyst Substances 0.000 claims 3
- ROORDVPLFPIABK-UHFFFAOYSA-N diphenyl carbonate Chemical compound C=1C=CC=CC=1OC(=O)OC1=CC=CC=C1 ROORDVPLFPIABK-UHFFFAOYSA-N 0.000 claims 3
- 239000000203 mixture Substances 0.000 claims 3
- 239000002904 solvent Substances 0.000 claims 3
- QIGBRXMKCJKVMJ-UHFFFAOYSA-N Hydroquinone Chemical compound OC1=CC=C(O)C=C1 QIGBRXMKCJKVMJ-UHFFFAOYSA-N 0.000 claims 2
- YGYAWVDWMABLBF-UHFFFAOYSA-N Phosgene Chemical group ClC(Cl)=O YGYAWVDWMABLBF-UHFFFAOYSA-N 0.000 claims 2
- ATUOYWHBWRKTHZ-UHFFFAOYSA-N Propane Chemical compound CCC ATUOYWHBWRKTHZ-UHFFFAOYSA-N 0.000 claims 2
- -1 bisphenol compound Chemical class 0.000 claims 2
- MJMCZNIYAWSFMG-UHFFFAOYSA-M butanoate;tetraethylphosphanium Chemical compound CCCC([O-])=O.CC[P+](CC)(CC)CC MJMCZNIYAWSFMG-UHFFFAOYSA-M 0.000 claims 2
- JOOJYKLPEQLDIH-UHFFFAOYSA-M butanoate;tetramethylphosphanium Chemical compound C[P+](C)(C)C.CCCC([O-])=O JOOJYKLPEQLDIH-UHFFFAOYSA-M 0.000 claims 2
- OGMLZMYAFPYSTM-UHFFFAOYSA-M butanoate;tetrapropylphosphanium Chemical compound CCCC([O-])=O.CCC[P+](CCC)(CCC)CCC OGMLZMYAFPYSTM-UHFFFAOYSA-M 0.000 claims 2
- QPTUMKXXAAHOOE-UHFFFAOYSA-M cesium;hydron;phosphate Chemical compound [Cs+].OP(O)([O-])=O QPTUMKXXAAHOOE-UHFFFAOYSA-M 0.000 claims 2
- 150000002430 hydrocarbons Chemical group 0.000 claims 2
- SIAPCJWMELPYOE-UHFFFAOYSA-N lithium hydride Chemical compound [LiH] SIAPCJWMELPYOE-UHFFFAOYSA-N 0.000 claims 2
- 229910000103 lithium hydride Inorganic materials 0.000 claims 2
- 238000004519 manufacturing process Methods 0.000 claims 2
- 239000003607 modifier Substances 0.000 claims 2
- PXBGQFYGVFUKNE-UHFFFAOYSA-N phosphanium;acetate Chemical compound [PH4+].CC([O-])=O PXBGQFYGVFUKNE-UHFFFAOYSA-N 0.000 claims 2
- OGPGZJLEIDWRHR-UHFFFAOYSA-M propanoate;tetraethylphosphanium Chemical compound CCC([O-])=O.CC[P+](CC)(CC)CC OGPGZJLEIDWRHR-UHFFFAOYSA-M 0.000 claims 2
- OYNYQOJNEQMVMJ-UHFFFAOYSA-M propanoate;tetramethylphosphanium Chemical compound CCC([O-])=O.C[P+](C)(C)C OYNYQOJNEQMVMJ-UHFFFAOYSA-M 0.000 claims 2
- OZZLCABNCRUDDM-UHFFFAOYSA-M propanoate;tetrapropylphosphanium Chemical compound CCC([O-])=O.CCC[P+](CCC)(CCC)CCC OZZLCABNCRUDDM-UHFFFAOYSA-M 0.000 claims 2
- 239000013557 residual solvent Substances 0.000 claims 2
- KIMPPGSMONZDMN-UHFFFAOYSA-N sodium;dihydrogen phosphite Chemical compound [Na+].OP(O)[O-] KIMPPGSMONZDMN-UHFFFAOYSA-N 0.000 claims 2
- GFZMLBWMGBLIDI-UHFFFAOYSA-M tetrabutylphosphanium;acetate Chemical compound CC([O-])=O.CCCC[P+](CCCC)(CCCC)CCCC GFZMLBWMGBLIDI-UHFFFAOYSA-M 0.000 claims 2
- QRMVDQYAEDLBBL-UHFFFAOYSA-N tetradecylphosphanium;acetate Chemical compound CC([O-])=O.CCCCCCCCCCCCCC[PH3+] QRMVDQYAEDLBBL-UHFFFAOYSA-N 0.000 claims 2
- WPNCRHWFQAPURM-UHFFFAOYSA-M tetradodecylphosphanium;acetate Chemical compound CC([O-])=O.CCCCCCCCCCCC[P+](CCCCCCCCCCCC)(CCCCCCCCCCCC)CCCCCCCCCCCC WPNCRHWFQAPURM-UHFFFAOYSA-M 0.000 claims 2
- ZZSILJPVLCLAMM-UHFFFAOYSA-M tetraethylphosphanium;benzoate Chemical compound CC[P+](CC)(CC)CC.[O-]C(=O)C1=CC=CC=C1 ZZSILJPVLCLAMM-UHFFFAOYSA-M 0.000 claims 2
- YUKNWAMYDSSWLX-UHFFFAOYSA-M tetraethylphosphanium;formate Chemical compound [O-]C=O.CC[P+](CC)(CC)CC YUKNWAMYDSSWLX-UHFFFAOYSA-M 0.000 claims 2
- TWTUOHYFCYGNFR-UHFFFAOYSA-M tetraheptylphosphanium;acetate Chemical compound CC([O-])=O.CCCCCCC[P+](CCCCCCC)(CCCCCCC)CCCCCCC TWTUOHYFCYGNFR-UHFFFAOYSA-M 0.000 claims 2
- HYVDRSVZYMKTKG-UHFFFAOYSA-M tetramethylphosphanium;acetate Chemical compound CC([O-])=O.C[P+](C)(C)C HYVDRSVZYMKTKG-UHFFFAOYSA-M 0.000 claims 2
- ZPRWYZRUPRQWKR-UHFFFAOYSA-M tetramethylphosphanium;formate Chemical compound [O-]C=O.C[P+](C)(C)C ZPRWYZRUPRQWKR-UHFFFAOYSA-M 0.000 claims 2
- NCYWEOAYLCHMDJ-UHFFFAOYSA-M tetraoctylphosphanium;acetate Chemical compound CC([O-])=O.CCCCCCCC[P+](CCCCCCCC)(CCCCCCCC)CCCCCCCC NCYWEOAYLCHMDJ-UHFFFAOYSA-M 0.000 claims 2
- RWJJQUSSNFANHY-UHFFFAOYSA-M tetrapentylphosphanium;acetate Chemical compound CC([O-])=O.CCCCC[P+](CCCCC)(CCCCC)CCCCC RWJJQUSSNFANHY-UHFFFAOYSA-M 0.000 claims 2
- HLNHDVOODYDVRZ-UHFFFAOYSA-M tetraphenylphosphanium;acetate Chemical compound CC([O-])=O.C1=CC=CC=C1[P+](C=1C=CC=CC=1)(C=1C=CC=CC=1)C1=CC=CC=C1 HLNHDVOODYDVRZ-UHFFFAOYSA-M 0.000 claims 2
- FOUUISAQGPLIMM-UHFFFAOYSA-M tetraphenylphosphanium;benzoate Chemical compound [O-]C(=O)C1=CC=CC=C1.C1=CC=CC=C1[P+](C=1C=CC=CC=1)(C=1C=CC=CC=1)C1=CC=CC=C1 FOUUISAQGPLIMM-UHFFFAOYSA-M 0.000 claims 2
- VLDHXZBAXRDKQN-UHFFFAOYSA-M tetraphenylphosphanium;formate Chemical compound [O-]C=O.C1=CC=CC=C1[P+](C=1C=CC=CC=1)(C=1C=CC=CC=1)C1=CC=CC=C1 VLDHXZBAXRDKQN-UHFFFAOYSA-M 0.000 claims 2
- LEAIJASTTLNZRQ-UHFFFAOYSA-M tetrapropylphosphanium;acetate Chemical compound CC([O-])=O.CCC[P+](CCC)(CCC)CCC LEAIJASTTLNZRQ-UHFFFAOYSA-M 0.000 claims 2
- JUPOUKRNSISUMS-UHFFFAOYSA-M tetrapropylphosphanium;benzoate Chemical compound [O-]C(=O)C1=CC=CC=C1.CCC[P+](CCC)(CCC)CCC JUPOUKRNSISUMS-UHFFFAOYSA-M 0.000 claims 2
- PDFVBAOUJUEEBM-UHFFFAOYSA-M tetrapropylphosphanium;formate Chemical compound [O-]C=O.CCC[P+](CCC)(CCC)CCC PDFVBAOUJUEEBM-UHFFFAOYSA-M 0.000 claims 2
- 238000005809 transesterification reaction Methods 0.000 claims 2
- ROFMCPHQNWGXGE-SFHVURJKSA-N (3s)-n-[2-[2-(dimethylamino)ethoxy]-4-(1h-pyrazol-4-yl)phenyl]-6-methoxy-3,4-dihydro-2h-chromene-3-carboxamide Chemical compound O=C([C@@H]1COC2=CC=C(C=C2C1)OC)NC(C(=C1)OCCN(C)C)=CC=C1C=1C=NNC=1 ROFMCPHQNWGXGE-SFHVURJKSA-N 0.000 claims 1
- GZFGOTFRPZRKDS-UHFFFAOYSA-N 4-bromophenol Chemical compound OC1=CC=C(Br)C=C1 GZFGOTFRPZRKDS-UHFFFAOYSA-N 0.000 claims 1
- 125000004203 4-hydroxyphenyl group Chemical group [H]OC1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 claims 1
- QTBSBXVTEAMEQO-UHFFFAOYSA-M Acetate Chemical compound CC([O-])=O QTBSBXVTEAMEQO-UHFFFAOYSA-M 0.000 claims 1
- 229930185605 Bisphenol Natural products 0.000 claims 1
- WKBOTKDWSSQWDR-UHFFFAOYSA-N Bromine atom Chemical compound [Br] WKBOTKDWSSQWDR-UHFFFAOYSA-N 0.000 claims 1
- ZAMOUSCENKQFHK-UHFFFAOYSA-N Chlorine atom Chemical compound [Cl] ZAMOUSCENKQFHK-UHFFFAOYSA-N 0.000 claims 1
- MJOQJPYNENPSSS-XQHKEYJVSA-N [(3r,4s,5r,6s)-4,5,6-triacetyloxyoxan-3-yl] acetate Chemical compound CC(=O)O[C@@H]1CO[C@@H](OC(C)=O)[C@H](OC(C)=O)[C@H]1OC(C)=O MJOQJPYNENPSSS-XQHKEYJVSA-N 0.000 claims 1
- 239000002253 acid Substances 0.000 claims 1
- POZGCGJFBOZPCM-UHFFFAOYSA-N bis(2-methylphenyl) carbonate Chemical compound CC1=CC=CC=C1OC(=O)OC1=CC=CC=C1C POZGCGJFBOZPCM-UHFFFAOYSA-N 0.000 claims 1
- GDTBXPJZTBHREO-UHFFFAOYSA-N bromine Substances BrBr GDTBXPJZTBHREO-UHFFFAOYSA-N 0.000 claims 1
- 229910052794 bromium Inorganic materials 0.000 claims 1
- AXCZMVOFGPJBDE-UHFFFAOYSA-L calcium dihydroxide Chemical compound [OH-].[OH-].[Ca+2] AXCZMVOFGPJBDE-UHFFFAOYSA-L 0.000 claims 1
- 239000000920 calcium hydroxide Substances 0.000 claims 1
- 229910001861 calcium hydroxide Inorganic materials 0.000 claims 1
- 125000004432 carbon atom Chemical group C* 0.000 claims 1
- MOIPGXQKZSZOQX-UHFFFAOYSA-N carbonyl bromide Chemical compound BrC(Br)=O MOIPGXQKZSZOQX-UHFFFAOYSA-N 0.000 claims 1
- 238000006243 chemical reaction Methods 0.000 claims 1
- 239000000460 chlorine Substances 0.000 claims 1
- 229910052801 chlorine Inorganic materials 0.000 claims 1
- 125000000753 cycloalkyl group Chemical group 0.000 claims 1
- ZQUZPFYNEARCQO-UHFFFAOYSA-N dinaphthalen-1-yl carbonate Chemical compound C1=CC=C2C(OC(OC=3C4=CC=CC=C4C=CC=3)=O)=CC=CC2=C1 ZQUZPFYNEARCQO-UHFFFAOYSA-N 0.000 claims 1
- 125000004435 hydrogen atom Chemical group [H]* 0.000 claims 1
- SLCVBVWXLSEKPL-UHFFFAOYSA-N neopentyl glycol Chemical compound OCC(C)(C)CO SLCVBVWXLSEKPL-UHFFFAOYSA-N 0.000 claims 1
- YCWSUKQGVSGXJO-NTUHNPAUSA-N nifuroxazide Chemical group C1=CC(O)=CC=C1C(=O)N\N=C\C1=CC=C([N+]([O-])=O)O1 YCWSUKQGVSGXJO-NTUHNPAUSA-N 0.000 claims 1
- QBDSZLJBMIMQRS-UHFFFAOYSA-N p-Cumylphenol Chemical compound C=1C=C(O)C=CC=1C(C)(C)C1=CC=CC=C1 QBDSZLJBMIMQRS-UHFFFAOYSA-N 0.000 claims 1
- NKTOLZVEWDHZMU-UHFFFAOYSA-N p-cumyl phenol Natural products CC1=CC=C(C)C(O)=C1 NKTOLZVEWDHZMU-UHFFFAOYSA-N 0.000 claims 1
- 239000001294 propane Substances 0.000 claims 1
- 150000003856 quaternary ammonium compounds Chemical class 0.000 claims 1
- 150000004023 quaternary phosphonium compounds Chemical class 0.000 claims 1
- JRQMGUGXUVNKFF-UHFFFAOYSA-M tetraethylphosphanium;acetate Chemical compound CC([O-])=O.CC[P+](CC)(CC)CC JRQMGUGXUVNKFF-UHFFFAOYSA-M 0.000 claims 1
- ZENSRGQTDKTDOJ-UHFFFAOYSA-M tetrahexylphosphanium;acetate Chemical compound CC([O-])=O.CCCCCC[P+](CCCCCC)(CCCCCC)CCCCCC ZENSRGQTDKTDOJ-UHFFFAOYSA-M 0.000 claims 1
- WPBUQRHEZCJFHK-UHFFFAOYSA-M tetramethylphosphanium;benzoate Chemical compound C[P+](C)(C)C.[O-]C(=O)C1=CC=CC=C1 WPBUQRHEZCJFHK-UHFFFAOYSA-M 0.000 claims 1
Applications Claiming Priority (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US10/248,147 US7122613B1 (en) | 2002-12-20 | 2002-12-20 | Method for the production of polycarbonates |
| PCT/US2003/039177 WO2004060963A1 (en) | 2002-12-20 | 2003-12-09 | Method for the production of polycarbonates |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| JP2006511667A JP2006511667A (ja) | 2006-04-06 |
| JP2006511667A5 true JP2006511667A5 (enExample) | 2007-02-08 |
Family
ID=32710618
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP2004565308A Withdrawn JP2006511667A (ja) | 2002-12-20 | 2003-12-09 | ポリカーボネートの製造方法 |
Country Status (7)
| Country | Link |
|---|---|
| US (1) | US7122613B1 (enExample) |
| EP (1) | EP1578840A1 (enExample) |
| JP (1) | JP2006511667A (enExample) |
| CN (1) | CN100537635C (enExample) |
| AU (1) | AU2003293477A1 (enExample) |
| TW (1) | TW200422318A (enExample) |
| WO (1) | WO2004060963A1 (enExample) |
Families Citing this family (10)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JP4490703B2 (ja) * | 2004-02-26 | 2010-06-30 | 出光興産株式会社 | ポリカーボネートの製造方法 |
| KR101308580B1 (ko) * | 2009-09-03 | 2013-09-12 | 에스케이이노베이션 주식회사 | 지방족 폴리카보네이트의 연속 제조방법 |
| CN102120818B (zh) * | 2011-01-05 | 2012-08-01 | 河北工业大学 | 一种脂肪族聚碳酸酯二元醇的制备方法 |
| KR101697391B1 (ko) * | 2013-09-30 | 2017-02-01 | 주식회사 엘지화학 | 코폴리카보네이트 수지 및 이를 포함하는 성형품 |
| EP3052543B1 (en) * | 2013-09-30 | 2018-04-04 | SABIC Global Technologies B.V. | Process to prepare high heat polycarbonates |
| KR101755754B1 (ko) | 2013-10-01 | 2017-07-07 | 주식회사 엘지화학 | 코폴리카보네이트 수지 및 이를 포함하는 성형품 |
| ES2769084T3 (es) * | 2015-12-22 | 2020-06-24 | Shell Int Research | Método para producir policarbonato |
| CN109423032A (zh) * | 2017-09-05 | 2019-03-05 | 张家港市杨舍丝印工艺厂 | 一种二氧化硅-聚碳酸酯耐高温材料的制备方法 |
| KR102292023B1 (ko) * | 2019-10-30 | 2021-08-24 | 주식회사 삼양사 | 폴리카보네이트 수지 및 그 제조 방법 |
| CN117325485B (zh) * | 2023-11-30 | 2024-03-08 | 乌镇实验室 | 一种用于风电叶片的碳纤维增强聚酰胺复合材料及其制备方法 |
Family Cites Families (16)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US4217438A (en) | 1978-12-15 | 1980-08-12 | General Electric Company | Polycarbonate transesterification process |
| US4362829A (en) | 1981-08-26 | 1982-12-07 | General Electric Company | Polycarbonates stabilized with sulfolane derivatives |
| IT1207057B (it) | 1985-07-10 | 1989-05-17 | Sassari A | Policarbonati ramificati contenenti 2,4,6-tris(4'-idrossiaril)-ammino-s-triazine. |
| US4677183A (en) | 1985-11-12 | 1987-06-30 | General Electric Company | Polycarbonate exhibiting improved impact properties containing divalent residue of polymerized, partially hydrogenated conjugated alkadiene monomer |
| US4737573A (en) | 1986-10-10 | 1988-04-12 | General Electric Company | Method for polymerizing aromatic bischloroformate composition to polycarbonate |
| US4973664A (en) | 1989-07-20 | 1990-11-27 | General Electric Company | Method for preparing polycarbonates of controlled molecular weight from bischloroformates |
| DE3941014A1 (de) * | 1989-12-12 | 1991-06-13 | Bayer Ag | Zweistufen-verfahren zur herstellung von polycarbonaten auf basis von speziellen dihydroxydiphenylalkanen |
| US5132398A (en) * | 1991-02-15 | 1992-07-21 | General Electric Company | Preparation of linear polycarbonates from cyclic oligomer compositions using Wittig salt or precursors thereof as catalyst |
| US5597887A (en) | 1994-10-20 | 1997-01-28 | General Electric Company | Branched polycarbonate preforms, blow moldable polycarbonate and method for making |
| US5523379A (en) | 1994-12-21 | 1996-06-04 | General Electric Plastics | High molecular weight stabilizer compounds for stabilizing polymers |
| ES2218580T3 (es) * | 1995-01-31 | 2004-11-16 | Idemitsu Kosan Company Limited | Procedimiento para producir policarbonato. |
| EP0801089A1 (en) * | 1996-04-12 | 1997-10-15 | THE COUNCIL OF SCIENTIFIC & INDUSTRIAL RESEARCH | Preparation of branched polycarbonates |
| US5864006A (en) * | 1997-04-08 | 1999-01-26 | The Dow Chemical Company | Method of making polycarbonate prepolymer and method of making high molecular weight polycarbonate |
| JP4275228B2 (ja) * | 1998-03-26 | 2009-06-10 | 出光興産株式会社 | ポリカーボネートを製造する方法 |
| US6140457A (en) | 1999-02-26 | 2000-10-31 | General Electric Company | Static-resistant polycarbonates having DI-t-alkylphenyl end groups |
| JP4195145B2 (ja) * | 1999-04-01 | 2008-12-10 | 出光興産株式会社 | ポリカーボネートの製造方法 |
-
2002
- 2002-12-20 US US10/248,147 patent/US7122613B1/en not_active Expired - Fee Related
-
2003
- 2003-12-09 EP EP03790427A patent/EP1578840A1/en not_active Withdrawn
- 2003-12-09 CN CNB2003801094307A patent/CN100537635C/zh not_active Expired - Fee Related
- 2003-12-09 AU AU2003293477A patent/AU2003293477A1/en not_active Abandoned
- 2003-12-09 JP JP2004565308A patent/JP2006511667A/ja not_active Withdrawn
- 2003-12-09 WO PCT/US2003/039177 patent/WO2004060963A1/en not_active Ceased
- 2003-12-15 TW TW092135458A patent/TW200422318A/zh unknown
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