JP2001516753A5 - - Google Patents
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- Publication number
- JP2001516753A5 JP2001516753A5 JP2000511759A JP2000511759A JP2001516753A5 JP 2001516753 A5 JP2001516753 A5 JP 2001516753A5 JP 2000511759 A JP2000511759 A JP 2000511759A JP 2000511759 A JP2000511759 A JP 2000511759A JP 2001516753 A5 JP2001516753 A5 JP 2001516753A5
- Authority
- JP
- Japan
- Prior art keywords
- extraction solvent
- epoxide
- diluent
- mixture
- compound
- 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.)
- Granted
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- 238000000605 extraction Methods 0.000 description 10
- 238000000034 method Methods 0.000 description 10
- 239000002904 solvent Substances 0.000 description 10
- 239000000203 mixture Substances 0.000 description 9
- 150000002924 oxiranes Chemical class 0.000 description 9
- 239000003085 diluting agent Substances 0.000 description 8
- 238000004519 manufacturing process Methods 0.000 description 7
- 239000007795 chemical reaction product Substances 0.000 description 5
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 5
- MHAJPDPJQMAIIY-UHFFFAOYSA-N Hydrogen peroxide Chemical compound OO MHAJPDPJQMAIIY-UHFFFAOYSA-N 0.000 description 4
- 229910021536 Zeolite Inorganic materials 0.000 description 4
- 150000001875 compounds Chemical class 0.000 description 4
- -1 peroxide compounds Chemical class 0.000 description 4
- 239000010457 zeolite Substances 0.000 description 4
- 150000001336 alkenes Chemical class 0.000 description 3
- 125000004432 carbon atom Chemical group C* 0.000 description 3
- 238000004821 distillation Methods 0.000 description 3
- JRZJOMJEPLMPRA-UHFFFAOYSA-N olefin Natural products CCCCCCCC=C JRZJOMJEPLMPRA-UHFFFAOYSA-N 0.000 description 3
- 239000000376 reactant Substances 0.000 description 3
- CFXQEHVMCRXUSD-UHFFFAOYSA-N 1,2,3-Trichloropropane Chemical compound ClCC(Cl)CCl CFXQEHVMCRXUSD-UHFFFAOYSA-N 0.000 description 2
- RFFLAFLAYFXFSW-UHFFFAOYSA-N 1,2-dichlorobenzene Chemical compound ClC1=CC=CC=C1Cl RFFLAFLAYFXFSW-UHFFFAOYSA-N 0.000 description 2
- AUHZEENZYGFFBQ-UHFFFAOYSA-N 1,3,5-trimethylbenzene Chemical compound CC1=CC(C)=CC(C)=C1 AUHZEENZYGFFBQ-UHFFFAOYSA-N 0.000 description 2
- OSDWBNJEKMUWAV-UHFFFAOYSA-N Allyl chloride Chemical compound ClCC=C OSDWBNJEKMUWAV-UHFFFAOYSA-N 0.000 description 2
- 238000009835 boiling Methods 0.000 description 2
- 239000003054 catalyst Substances 0.000 description 2
- NNBZCPXTIHJBJL-UHFFFAOYSA-N decalin Chemical compound C1CCCC2CCCCC21 NNBZCPXTIHJBJL-UHFFFAOYSA-N 0.000 description 2
- DIOQZVSQGTUSAI-UHFFFAOYSA-N decane Chemical compound CCCCCCCCCC DIOQZVSQGTUSAI-UHFFFAOYSA-N 0.000 description 2
- HNPSIPDUKPIQMN-UHFFFAOYSA-N dioxosilane;oxo(oxoalumanyloxy)alumane Chemical compound O=[Si]=O.O=[Al]O[Al]=O HNPSIPDUKPIQMN-UHFFFAOYSA-N 0.000 description 2
- 239000007788 liquid Substances 0.000 description 2
- 239000007791 liquid phase Substances 0.000 description 2
- LQNUZADURLCDLV-UHFFFAOYSA-N nitrobenzene Chemical compound [O-][N+](=O)C1=CC=CC=C1 LQNUZADURLCDLV-UHFFFAOYSA-N 0.000 description 2
- ZPQOPVIELGIULI-UHFFFAOYSA-N 1,3-dichlorobenzene Chemical compound ClC1=CC=CC(Cl)=C1 ZPQOPVIELGIULI-UHFFFAOYSA-N 0.000 description 1
- IBSQPLPBRSHTTG-UHFFFAOYSA-N 1-chloro-2-methylbenzene Chemical compound CC1=CC=CC=C1Cl IBSQPLPBRSHTTG-UHFFFAOYSA-N 0.000 description 1
- BRLQWZUYTZBJKN-UHFFFAOYSA-N Epichlorohydrin Chemical compound ClCC1CO1 BRLQWZUYTZBJKN-UHFFFAOYSA-N 0.000 description 1
- GOOHAUXETOMSMM-UHFFFAOYSA-N Propylene oxide Chemical group CC1CO1 GOOHAUXETOMSMM-UHFFFAOYSA-N 0.000 description 1
- 125000003158 alcohol group Chemical group 0.000 description 1
- 125000000217 alkyl group Chemical group 0.000 description 1
- 150000004945 aromatic hydrocarbons Chemical class 0.000 description 1
- 229910052736 halogen Inorganic materials 0.000 description 1
- 150000002367 halogens Chemical class 0.000 description 1
- 238000000622 liquid--liquid extraction Methods 0.000 description 1
- QJGQUHMNIGDVPM-UHFFFAOYSA-N nitrogen group Chemical group [N] QJGQUHMNIGDVPM-UHFFFAOYSA-N 0.000 description 1
- QQONPFPTGQHPMA-UHFFFAOYSA-N propylene Natural products CC=C QQONPFPTGQHPMA-UHFFFAOYSA-N 0.000 description 1
- 125000004805 propylene group Chemical group [H]C([H])([H])C([H])([*:1])C([H])([H])[*:2] 0.000 description 1
- 229930195734 saturated hydrocarbon Natural products 0.000 description 1
- 238000000638 solvent extraction Methods 0.000 description 1
- 229930195735 unsaturated hydrocarbon Natural products 0.000 description 1
- PXXNTAGJWPJAGM-UHFFFAOYSA-N vertaline Natural products C1C2C=3C=C(OC)C(OC)=CC=3OC(C=C3)=CC=C3CCC(=O)OC1CC1N2CCCC1 PXXNTAGJWPJAGM-UHFFFAOYSA-N 0.000 description 1
Applications Claiming Priority (3)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| BE9700756 | 1997-09-18 | ||
| BE9700756A BE1011456A3 (fr) | 1997-09-18 | 1997-09-18 | Procede de fabrication d'un oxiranne. |
| PCT/EP1998/005750 WO1999014208A1 (fr) | 1997-09-18 | 1998-09-10 | Procede de fabrication d'un oxiranne |
Related Child Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP2010063944A Division JP2010159281A (ja) | 1997-09-18 | 2010-03-19 | エポキシド製造法 |
Publications (3)
| Publication Number | Publication Date |
|---|---|
| JP2001516753A JP2001516753A (ja) | 2001-10-02 |
| JP2001516753A5 true JP2001516753A5 (enExample) | 2006-01-05 |
| JP5073132B2 JP5073132B2 (ja) | 2012-11-14 |
Family
ID=3890733
Family Applications (2)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP2000511759A Expired - Fee Related JP5073132B2 (ja) | 1997-09-18 | 1998-09-10 | エポキシド製造法 |
| JP2010063944A Pending JP2010159281A (ja) | 1997-09-18 | 2010-03-19 | エポキシド製造法 |
Family Applications After (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP2010063944A Pending JP2010159281A (ja) | 1997-09-18 | 2010-03-19 | エポキシド製造法 |
Country Status (10)
| Country | Link |
|---|---|
| US (1) | US6350888B1 (enExample) |
| EP (1) | EP1017686A1 (enExample) |
| JP (2) | JP5073132B2 (enExample) |
| AR (1) | AR023007A1 (enExample) |
| AU (1) | AU9742598A (enExample) |
| BE (1) | BE1011456A3 (enExample) |
| BR (1) | BR9812516A (enExample) |
| SA (1) | SA98190748B1 (enExample) |
| WO (1) | WO1999014208A1 (enExample) |
| ZA (1) | ZA988398B (enExample) |
Families Citing this family (43)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| EP1122249A1 (fr) | 2000-02-02 | 2001-08-08 | SOLVAY (Société Anonyme) | Procédé de fabrication d'un oxiranne |
| EP1420014A4 (en) * | 2001-08-22 | 2004-09-29 | Sumitomo Chemical Co | PROCESS FOR PRODUCING PROPYLENE OXIDE |
| FR2846964B1 (fr) * | 2002-11-12 | 2006-07-21 | Procede de fabrication de 1,2-epoxy-3-chloropropane | |
| FR2846965B1 (fr) * | 2002-11-12 | 2006-10-13 | Procede de fabrication de 1,2-epoxy-3-chloropropane | |
| US7169945B2 (en) | 2002-11-26 | 2007-01-30 | Degussa Ag | Process for the epoxidation of olefins |
| US7531674B2 (en) | 2003-03-06 | 2009-05-12 | Sumitomo Chemical Company, Limited | Process for producing propylene oxide |
| EP1770081A1 (en) * | 2003-11-20 | 2007-04-04 | SOLVAY (Société Anonyme) | Process for producing dichloropropanol from glycerol , the glycerol coming eventualy from the conversion of animal fats in the manufacture of biodiesel |
| KR20080037615A (ko) | 2005-05-20 | 2008-04-30 | 솔베이(소시에떼아노님) | 클로로히드린의 제조 방법 |
| US20080214848A1 (en) * | 2005-05-20 | 2008-09-04 | Solvay (Societe Anonyme) | Method For Making an Epoxy Starting From a Chlorhydrine |
| BRPI0618325A2 (pt) * | 2005-11-08 | 2011-08-23 | Solvay | processo parar a produção de dicloropropanol |
| EP2043984A1 (en) * | 2006-06-14 | 2009-04-08 | Solvay S.A. | Crude glycerol-based product, process for its purification and its use in the manufacture of dichloropropanol |
| KR100846435B1 (ko) * | 2006-12-22 | 2008-07-16 | 한화석유화학 주식회사 | 옥시란 화합물의 제조 방법 |
| US20100032617A1 (en) * | 2007-02-20 | 2010-02-11 | Solvay (Societe Anonyme) | Process for manufacturing epichlorohydrin |
| FR2913421B1 (fr) * | 2007-03-07 | 2009-05-15 | Solvay | Procede de fabrication de dichloropropanol. |
| FR2913684B1 (fr) | 2007-03-14 | 2012-09-14 | Solvay | Procede de fabrication de dichloropropanol |
| CN101293882B (zh) * | 2007-04-24 | 2011-04-20 | 中国石油化工股份有限公司 | 一种环氧氯丙烷的分离方法 |
| TW200911740A (en) | 2007-06-01 | 2009-03-16 | Solvay | Process for manufacturing a chlorohydrin |
| TWI500609B (zh) * | 2007-06-12 | 2015-09-21 | Solvay | 含有環氧氯丙烷的產品，其製備及其不同應用中的用途 |
| TW200911693A (en) | 2007-06-12 | 2009-03-16 | Solvay | Aqueous composition containing a salt, manufacturing process and use |
| KR20100089835A (ko) * | 2007-10-02 | 2010-08-12 | 솔베이(소시에떼아노님) | 용기의 내부식성 향상을 위한 실리콘-함유 조성물의 용도 |
| FR2925045B1 (fr) | 2007-12-17 | 2012-02-24 | Solvay | Produit a base de glycerol, procede pour son obtention et son utilisation dans la fabrication de dichloropropanol |
| TWI478875B (zh) * | 2008-01-31 | 2015-04-01 | Solvay | 使水性組成物中之有機物質降解之方法 |
| EP2103604A1 (de) * | 2008-03-17 | 2009-09-23 | Evonik Degussa GmbH | Verfahren zur Herstellung von Epichlorhydrin |
| JP5619721B2 (ja) | 2008-04-03 | 2014-11-05 | ソルヴェイ（ソシエテ アノニム） | グリセロールを含む組成物、それを得る方法およびジクロロプロパノールの製造でのその使用 |
| EP2149569A1 (en) * | 2008-08-01 | 2010-02-03 | Hexion Specialty Chemicals Research Belgium S.A. | Process for the manufacture of a 1,2-Epoxide |
| EP2149570A1 (en) * | 2008-08-01 | 2010-02-03 | Hexion Specialty Chemicals Research Belgium S.A. | Process for the manufacture of epichlorohydrin using hydrogen peroxide and a manganese komplex |
| FR2935968B1 (fr) | 2008-09-12 | 2010-09-10 | Solvay | Procede pour la purification de chlorure d'hydrogene |
| CN101880263B (zh) * | 2009-05-09 | 2012-07-11 | 中国石油化工集团公司 | 一种环氧氯丙烷的制备方法 |
| MX2012000556A (es) * | 2009-07-16 | 2012-04-11 | Basf Se | Metodo para la separacion de acetonitrilo a partir de agua. |
| EP2343288A1 (en) | 2009-11-27 | 2011-07-13 | Momentive Specialty Chemicals Research Belgium S.A. | Process for the manufacture of propylene oxide |
| EP2354131A1 (en) | 2010-02-02 | 2011-08-10 | Momentive Specialty Chemicals Research Belgium | Process for the manufacture of a 1,2-epoxide and a device for carrying out said process |
| KR20140009163A (ko) | 2010-09-30 | 2014-01-22 | 솔베이(소시에떼아노님) | 천연유래 에피클로로히드린의 유도체 |
| FR2966825B1 (fr) * | 2010-10-29 | 2014-05-16 | Solvay | Procede de fabrication d'epichlorhydrine |
| EA201391089A1 (ru) | 2011-01-27 | 2014-06-30 | Солвей Са | Способ изготовления 1,2-эпокси-3-хлорпропана |
| EA201391090A1 (ru) | 2011-01-27 | 2013-12-30 | Солвей Са | Способ получения 1,2-эпокси-3-хлорпропана |
| CN105439983A (zh) * | 2011-02-04 | 2016-03-30 | 蓝立方知识产权有限责任公司 | 混合物的相分离 |
| CN103420949B (zh) * | 2012-05-18 | 2016-05-25 | 中国石油化工股份有限公司 | 一种环氧氯丙烷的分离方法 |
| CN103420948B (zh) * | 2012-05-18 | 2016-05-25 | 中国石油化工股份有限公司 | 一种环氧氯丙烷的分离方法 |
| CN103420947B (zh) * | 2012-05-18 | 2016-07-06 | 中国石油化工股份有限公司 | 一种环氧氯丙烷的分离方法 |
| CN103420946B (zh) * | 2012-05-18 | 2016-08-03 | 中国石油化工股份有限公司 | 一种环氧氯丙烷的分离方法 |
| CN104003961B (zh) * | 2013-02-27 | 2016-05-25 | 中国石油化工股份有限公司 | 一种连续萃取环氧氯丙烷的方法 |
| EP3059228A1 (en) | 2015-02-17 | 2016-08-24 | Evonik Degussa GmbH | Method for the epoxidation of allyl chloride with hydrogen peroxide |
| CN111592506A (zh) * | 2020-06-02 | 2020-08-28 | 中国科学院理化技术研究所 | 环氧氯丙烷分离工艺 |
Family Cites Families (9)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US3541114A (en) * | 1967-01-13 | 1970-11-17 | Celanese Corp | Recovery of hydrophobic oxirane compounds |
| IT1122214B (it) * | 1979-07-19 | 1986-04-23 | Donegani Guido Ist | Processo per l'epossidazione catalitica di olefine con acqua ossigenata |
| US4379025A (en) * | 1982-05-24 | 1983-04-05 | Atlantic Richfield Company | Water removal from butylene oxides by liquid extraction with selected extractive solvents |
| IT1152299B (it) | 1982-07-28 | 1986-12-31 | Anic Spa | Procedimento per l'espossidazione di composti olefinici |
| US5127997A (en) * | 1991-05-09 | 1992-07-07 | Texaco Chemical Company | Purification of propylene oxide by liquid extraction |
| JPH05237392A (ja) * | 1992-02-24 | 1993-09-17 | Tosoh Corp | 酸化触媒およびエポキシ化法 |
| US5262550A (en) * | 1992-04-30 | 1993-11-16 | Arco Chemical Technology, L.P. | Epoxidation process using titanium-rich silicalite catalysts |
| US5412122A (en) * | 1993-12-23 | 1995-05-02 | Arco Chemical Technology, L.P. | Epoxidation process |
| US5646314A (en) * | 1994-11-16 | 1997-07-08 | Arco Chemical Technology, L.P. | Process for titanium silicalite-catalyzed epoxidation |
-
1997
- 1997-09-18 BE BE9700756A patent/BE1011456A3/fr active
-
1998
- 1998-09-10 JP JP2000511759A patent/JP5073132B2/ja not_active Expired - Fee Related
- 1998-09-10 AU AU97425/98A patent/AU9742598A/en not_active Abandoned
- 1998-09-10 US US09/508,731 patent/US6350888B1/en not_active Expired - Lifetime
- 1998-09-10 WO PCT/EP1998/005750 patent/WO1999014208A1/fr not_active Ceased
- 1998-09-10 EP EP98951373A patent/EP1017686A1/fr not_active Withdrawn
- 1998-09-10 BR BR9812516-8A patent/BR9812516A/pt not_active IP Right Cessation
- 1998-09-14 ZA ZA9808398A patent/ZA988398B/xx unknown
- 1998-09-17 AR ARP980104648A patent/AR023007A1/es not_active Application Discontinuation
- 1998-11-14 SA SA98190748A patent/SA98190748B1/ar unknown
-
2010
- 2010-03-19 JP JP2010063944A patent/JP2010159281A/ja active Pending
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