ZA200300106B - Method for the production of propylene oxide. - Google Patents
Method for the production of propylene oxide. Download PDFInfo
- Publication number
- ZA200300106B ZA200300106B ZA200300106A ZA200300106A ZA200300106B ZA 200300106 B ZA200300106 B ZA 200300106B ZA 200300106 A ZA200300106 A ZA 200300106A ZA 200300106 A ZA200300106 A ZA 200300106A ZA 200300106 B ZA200300106 B ZA 200300106B
- Authority
- ZA
- South Africa
- Prior art keywords
- mixture
- methanol
- propylene oxide
- separated
- gii
- Prior art date
Links
- 238000000034 method Methods 0.000 title claims abstract description 88
- GOOHAUXETOMSMM-UHFFFAOYSA-N Propylene oxide Chemical compound CC1CO1 GOOHAUXETOMSMM-UHFFFAOYSA-N 0.000 title claims abstract description 38
- OKKJLVBELUTLKV-UHFFFAOYSA-N Methanol Chemical compound OC OKKJLVBELUTLKV-UHFFFAOYSA-N 0.000 claims abstract description 252
- 239000000203 mixture Substances 0.000 claims abstract description 100
- 230000008569 process Effects 0.000 claims abstract description 66
- QQONPFPTGQHPMA-UHFFFAOYSA-N Propene Chemical compound CC=C QQONPFPTGQHPMA-UHFFFAOYSA-N 0.000 claims abstract description 62
- MHAJPDPJQMAIIY-UHFFFAOYSA-N Hydrogen peroxide Chemical compound OO MHAJPDPJQMAIIY-UHFFFAOYSA-N 0.000 claims abstract description 60
- TZIHFWKZFHZASV-UHFFFAOYSA-N methyl formate Chemical compound COC=O TZIHFWKZFHZASV-UHFFFAOYSA-N 0.000 claims abstract description 60
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 claims abstract description 27
- 238000002360 preparation method Methods 0.000 claims abstract description 16
- 238000004821 distillation Methods 0.000 claims description 34
- 238000006243 chemical reaction Methods 0.000 claims description 32
- 239000010457 zeolite Substances 0.000 claims description 16
- 239000003054 catalyst Substances 0.000 claims description 13
- 239000010936 titanium Substances 0.000 claims description 13
- RTAQQCXQSZGOHL-UHFFFAOYSA-N Titanium Chemical group [Ti] RTAQQCXQSZGOHL-UHFFFAOYSA-N 0.000 claims description 11
- 229910052719 titanium Inorganic materials 0.000 claims description 9
- HNPSIPDUKPIQMN-UHFFFAOYSA-N dioxosilane;oxo(oxoalumanyloxy)alumane Chemical compound O=[Si]=O.O=[Al]O[Al]=O HNPSIPDUKPIQMN-UHFFFAOYSA-N 0.000 claims description 7
- 229910021536 Zeolite Inorganic materials 0.000 claims description 6
- 238000000926 separation method Methods 0.000 description 13
- CSCPPACGZOOCGX-UHFFFAOYSA-N Acetone Chemical compound CC(C)=O CSCPPACGZOOCGX-UHFFFAOYSA-N 0.000 description 12
- 150000001875 compounds Chemical class 0.000 description 12
- 239000000047 product Substances 0.000 description 12
- 239000002904 solvent Substances 0.000 description 9
- 239000012535 impurity Substances 0.000 description 8
- 239000000543 intermediate Substances 0.000 description 8
- 239000002585 base Substances 0.000 description 7
- 238000009835 boiling Methods 0.000 description 7
- 238000011282 treatment Methods 0.000 description 7
- NBBJYMSMWIIQGU-UHFFFAOYSA-N Propionic aldehyde Chemical compound CCC=O NBBJYMSMWIIQGU-UHFFFAOYSA-N 0.000 description 6
- 239000007858 starting material Substances 0.000 description 6
- 239000000126 substance Substances 0.000 description 5
- SPEUIVXLLWOEMJ-UHFFFAOYSA-N 1,1-dimethoxyethane Chemical compound COC(C)OC SPEUIVXLLWOEMJ-UHFFFAOYSA-N 0.000 description 4
- QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical compound [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 description 4
- BDAGIHXWWSANSR-UHFFFAOYSA-N methanoic acid Natural products OC=O BDAGIHXWWSANSR-UHFFFAOYSA-N 0.000 description 4
- 239000001301 oxygen Substances 0.000 description 4
- 229910052760 oxygen Inorganic materials 0.000 description 4
- 238000010626 work up procedure Methods 0.000 description 4
- WEVYAHXRMPXWCK-UHFFFAOYSA-N Acetonitrile Chemical compound CC#N WEVYAHXRMPXWCK-UHFFFAOYSA-N 0.000 description 3
- RTZKZFJDLAIYFH-UHFFFAOYSA-N Diethyl ether Chemical compound CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 description 3
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 3
- ZMXDDKWLCZADIW-UHFFFAOYSA-N N,N-Dimethylformamide Chemical compound CN(C)C=O ZMXDDKWLCZADIW-UHFFFAOYSA-N 0.000 description 3
- DNIAPMSPPWPWGF-UHFFFAOYSA-N Propylene glycol Chemical compound CC(O)CO DNIAPMSPPWPWGF-UHFFFAOYSA-N 0.000 description 3
- IKHGUXGNUITLKF-XPULMUKRSA-N acetaldehyde Chemical compound [14CH]([14CH3])=O IKHGUXGNUITLKF-XPULMUKRSA-N 0.000 description 3
- 150000001298 alcohols Chemical class 0.000 description 3
- ZTQSAGDEMFDKMZ-UHFFFAOYSA-N butyric aldehyde Natural products CCCC=O ZTQSAGDEMFDKMZ-UHFFFAOYSA-N 0.000 description 3
- 239000006227 byproduct Substances 0.000 description 3
- 238000001816 cooling Methods 0.000 description 3
- 238000007700 distillative separation Methods 0.000 description 3
- 239000002638 heterogeneous catalyst Substances 0.000 description 3
- 239000002032 methanolic fraction Substances 0.000 description 3
- 239000012429 reaction media Substances 0.000 description 3
- ROSFUFIOLRQOON-UHFFFAOYSA-N 2,4-Dimethyl-1,3-dioxolane Chemical compound CC1COC(C)O1 ROSFUFIOLRQOON-UHFFFAOYSA-N 0.000 description 2
- 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 2
- YEJRWHAVMIAJKC-UHFFFAOYSA-N 4-Butyrolactone Chemical compound O=C1CCCO1 YEJRWHAVMIAJKC-UHFFFAOYSA-N 0.000 description 2
- VYZAMTAEIAYCRO-UHFFFAOYSA-N Chromium Chemical compound [Cr] VYZAMTAEIAYCRO-UHFFFAOYSA-N 0.000 description 2
- WYURNTSHIVDZCO-UHFFFAOYSA-N Tetrahydrofuran Chemical compound C1CCOC1 WYURNTSHIVDZCO-UHFFFAOYSA-N 0.000 description 2
- 239000002253 acid Substances 0.000 description 2
- 150000007513 acids Chemical class 0.000 description 2
- 229910052783 alkali metal Inorganic materials 0.000 description 2
- 150000001340 alkali metals Chemical class 0.000 description 2
- 150000007514 bases Chemical class 0.000 description 2
- 239000000470 constituent Substances 0.000 description 2
- 235000019253 formic acid Nutrition 0.000 description 2
- 150000002500 ions Chemical class 0.000 description 2
- 239000000463 material Substances 0.000 description 2
- VNWKTOKETHGBQD-UHFFFAOYSA-N methane Chemical compound C VNWKTOKETHGBQD-UHFFFAOYSA-N 0.000 description 2
- 238000011084 recovery Methods 0.000 description 2
- -1 wvanadium- Chemical compound 0.000 description 2
- UIOXNNAWANDJCZ-UHFFFAOYSA-N 1,1-dimethoxypropane Chemical compound CCC(OC)OC UIOXNNAWANDJCZ-UHFFFAOYSA-N 0.000 description 1
- LZDKZFUFMNSQCJ-UHFFFAOYSA-N 1,2-diethoxyethane Chemical compound CCOCCOCC LZDKZFUFMNSQCJ-UHFFFAOYSA-N 0.000 description 1
- WNXJIVFYUVYPPR-UHFFFAOYSA-N 1,3-dioxolane Chemical compound C1COCO1 WNXJIVFYUVYPPR-UHFFFAOYSA-N 0.000 description 1
- RYHBNJHYFVUHQT-UHFFFAOYSA-N 1,4-Dioxane Chemical compound C1COCCO1 RYHBNJHYFVUHQT-UHFFFAOYSA-N 0.000 description 1
- LHENQXAPVKABON-UHFFFAOYSA-N 1-methoxypropan-1-ol Chemical class CCC(O)OC LHENQXAPVKABON-UHFFFAOYSA-N 0.000 description 1
- XNWFRZJHXBZDAG-UHFFFAOYSA-N 2-METHOXYETHANOL Chemical compound COCCO XNWFRZJHXBZDAG-UHFFFAOYSA-N 0.000 description 1
- QCAHUFWKIQLBNB-UHFFFAOYSA-N 3-(3-methoxypropoxy)propan-1-ol Chemical compound COCCCOCCCO QCAHUFWKIQLBNB-UHFFFAOYSA-N 0.000 description 1
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 description 1
- BDAGIHXWWSANSR-UHFFFAOYSA-M Formate Chemical compound [O-]C=O BDAGIHXWWSANSR-UHFFFAOYSA-M 0.000 description 1
- VKEQBMCRQDSRET-UHFFFAOYSA-N Methylone Chemical compound CNC(C)C(=O)C1=CC=C2OCOC2=C1 VKEQBMCRQDSRET-UHFFFAOYSA-N 0.000 description 1
- FXHOOIRPVKKKFG-UHFFFAOYSA-N N,N-Dimethylacetamide Chemical compound CN(C)C(C)=O FXHOOIRPVKKKFG-UHFFFAOYSA-N 0.000 description 1
- LRHPLDYGYMQRHN-UHFFFAOYSA-N N-Butanol Chemical class CCCCO LRHPLDYGYMQRHN-UHFFFAOYSA-N 0.000 description 1
- SECXISVLQFMRJM-UHFFFAOYSA-N N-Methylpyrrolidone Chemical compound CN1CCCC1=O SECXISVLQFMRJM-UHFFFAOYSA-N 0.000 description 1
- AMQJEAYHLZJPGS-UHFFFAOYSA-N N-Pentanol Chemical class CCCCCO AMQJEAYHLZJPGS-UHFFFAOYSA-N 0.000 description 1
- BPQQTUXANYXVAA-UHFFFAOYSA-N Orthosilicate Chemical compound [O-][Si]([O-])([O-])[O-] BPQQTUXANYXVAA-UHFFFAOYSA-N 0.000 description 1
- XBDQKXXYIPTUBI-UHFFFAOYSA-M Propionate Chemical compound CCC([O-])=O XBDQKXXYIPTUBI-UHFFFAOYSA-M 0.000 description 1
- 238000002441 X-ray diffraction Methods 0.000 description 1
- QCWXUUIWCKQGHC-UHFFFAOYSA-N Zirconium Chemical compound [Zr] QCWXUUIWCKQGHC-UHFFFAOYSA-N 0.000 description 1
- KXKVLQRXCPHEJC-UHFFFAOYSA-N acetic acid trimethyl ester Natural products COC(C)=O KXKVLQRXCPHEJC-UHFFFAOYSA-N 0.000 description 1
- 229910000272 alkali metal oxide Inorganic materials 0.000 description 1
- 229910001860 alkaline earth metal hydroxide Inorganic materials 0.000 description 1
- 150000001336 alkenes Chemical class 0.000 description 1
- 229910052782 aluminium Inorganic materials 0.000 description 1
- XAGFODPZIPBFFR-UHFFFAOYSA-N aluminium Chemical compound [Al] XAGFODPZIPBFFR-UHFFFAOYSA-N 0.000 description 1
- 125000004429 atom Chemical group 0.000 description 1
- 229930188620 butyrolactone Natural products 0.000 description 1
- 229910052799 carbon Inorganic materials 0.000 description 1
- 125000004432 carbon atom Chemical group C* 0.000 description 1
- 238000009833 condensation Methods 0.000 description 1
- 230000005494 condensation Effects 0.000 description 1
- 239000013078 crystal Substances 0.000 description 1
- 238000010586 diagram Methods 0.000 description 1
- 229940113088 dimethylacetamide Drugs 0.000 description 1
- 238000000605 extraction Methods 0.000 description 1
- 238000000895 extractive distillation Methods 0.000 description 1
- 230000007062 hydrolysis Effects 0.000 description 1
- 238000006460 hydrolysis reaction Methods 0.000 description 1
- 230000010354 integration Effects 0.000 description 1
- WSFSSNUMVMOOMR-NJFSPNSNSA-N methanone Chemical compound O=[14CH2] WSFSSNUMVMOOMR-NJFSPNSNSA-N 0.000 description 1
- GFUGMBIZUXZOAF-UHFFFAOYSA-N niobium zirconium Chemical compound [Zr].[Nb] GFUGMBIZUXZOAF-UHFFFAOYSA-N 0.000 description 1
- 150000002989 phenols Chemical class 0.000 description 1
- 238000000053 physical method Methods 0.000 description 1
- 229920005862 polyol Polymers 0.000 description 1
- 150000003077 polyols Chemical class 0.000 description 1
- BDERNNFJNOPAEC-UHFFFAOYSA-N propan-1-ol Chemical class CCCO BDERNNFJNOPAEC-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
- 230000036647 reaction Effects 0.000 description 1
- 239000011369 resultant mixture Substances 0.000 description 1
- 150000003839 salts Chemical class 0.000 description 1
- YLQBMQCUIZJEEH-UHFFFAOYSA-N tetrahydrofuran Natural products C=1C=COC=1 YLQBMQCUIZJEEH-UHFFFAOYSA-N 0.000 description 1
- LEONUFNNVUYDNQ-UHFFFAOYSA-N vanadium atom Chemical compound [V] LEONUFNNVUYDNQ-UHFFFAOYSA-N 0.000 description 1
- 229910052726 zirconium Inorganic materials 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D301/00—Preparation of oxiranes
- C07D301/02—Synthesis of the oxirane ring
- C07D301/03—Synthesis of the oxirane ring by oxidation of unsaturated compounds, or of mixtures of unsaturated and saturated compounds
- C07D301/12—Synthesis of the oxirane ring by oxidation of unsaturated compounds, or of mixtures of unsaturated and saturated compounds with hydrogen peroxide or inorganic peroxides or peracids
-
- 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)
- Inorganic Chemistry (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
- Epoxy Compounds (AREA)
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| DE10032884A DE10032884A1 (de) | 2000-07-06 | 2000-07-06 | Verfahren zur Herstellung von Propylenoxid |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| ZA200300106B true ZA200300106B (en) | 2004-01-21 |
Family
ID=7648018
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| ZA200300106A ZA200300106B (en) | 2000-07-06 | 2003-01-06 | Method for the production of propylene oxide. |
Country Status (16)
| Country | Link |
|---|---|
| US (1) | US6756503B2 (zh) |
| EP (1) | EP1296968B1 (zh) |
| CN (1) | CN1230427C (zh) |
| AT (1) | ATE281442T1 (zh) |
| AU (1) | AU2001289624A1 (zh) |
| BR (1) | BR0112218A (zh) |
| CA (1) | CA2414756A1 (zh) |
| DE (2) | DE10032884A1 (zh) |
| IN (1) | IN2003CH00017A (zh) |
| MX (1) | MX237891B (zh) |
| MY (1) | MY126819A (zh) |
| RU (1) | RU2277089C2 (zh) |
| SA (1) | SA01220361B1 (zh) |
| TW (1) | TW583181B (zh) |
| WO (1) | WO2002002544A1 (zh) |
| ZA (1) | ZA200300106B (zh) |
Families Citing this family (32)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| ATE334992T1 (de) | 2001-04-30 | 2006-08-15 | Univ Michigan | Isoretikuläre organometallische grundstrukturen, verfahren zu deren bildung und systematische entwicklung von deren porengrösse und funktionalität, mit anwendung für die gasspeicherung |
| DE10143195A1 (de) * | 2001-09-04 | 2003-03-20 | Basf Ag | Integriertes Verfahren zur Herstellung von Polyurethan-Schäumen |
| DE10164348A1 (de) | 2001-12-28 | 2003-07-17 | Basf Ag | Verfahren zur Herstellung von 1-Methoypropanol-2 |
| DE10233386A1 (de) * | 2002-07-23 | 2004-02-12 | Basf Ag | Verfahren zur kontinuierlich betriebenen Reindestillation des bei der koppel-produktfreien Propylenoxidsynthese verwendeten Lösungsmittels Methanol unter gleichzeitiger Abtrennung der Methoxypropanole |
| DE10233381A1 (de) * | 2002-07-23 | 2004-01-29 | Basf Ag | Verfahren zur kontinuierlich betriebenen Destillation des bei der koppel-produktfreien Oxiransynthese verwendeten Lösungsmittels |
| DE10233388A1 (de) | 2002-07-23 | 2004-02-12 | Basf Ag | Verfahren zur kontinuierlich betriebenen Reindestillation des bei der koppel-produktfreien Propylenoxidsynthese verwendeten Lösungsmittels Methanol unter gleichzeitiger Abtrennung der Methoxypropanole und der Schwersieder |
| DE10240129B4 (de) | 2002-08-30 | 2004-11-11 | Basf Ag | Integriertes Verfahren zur Synthese von Propylenoxid |
| US7169945B2 (en) | 2002-11-26 | 2007-01-30 | Degussa Ag | Process for the epoxidation of olefins |
| KR101278432B1 (ko) | 2003-05-09 | 2013-07-04 | 더 리젠츠 오브 더 유니버시티 오브 미시간 | 결정들에서 우수한 수준의 표면적과 다공성의 성취를 위한 방법의 이행 |
| US20050004404A1 (en) | 2003-07-03 | 2005-01-06 | Basf Akiengesellschaft | Process for the alkoxylation of monools in the presence of metallo-organic framework materials |
| KR101108422B1 (ko) * | 2004-06-23 | 2012-01-30 | 스미또모 가가꾸 가부시키가이샤 | 프로필렌옥시드의 정제 방법 |
| JP5160893B2 (ja) | 2004-10-22 | 2013-03-13 | ザ リージェンツ オブ ザ ユニバーシティ オブ ミシガン | 共有結合性有機骨格及び多面体 |
| EP1828088B1 (de) | 2004-12-20 | 2008-02-27 | Evonik Degussa GmbH | Verfahren zur rückgewinnung von methanol |
| CN101084176B (zh) * | 2004-12-20 | 2012-12-05 | 赢创德固赛有限公司 | 回收甲醇的方法 |
| US20060161010A1 (en) * | 2005-01-18 | 2006-07-20 | Basf Aktiengesellschaft | Process for the epoxidation of an olefin with improved energy balance |
| KR101361402B1 (ko) | 2005-04-07 | 2014-02-10 | 더 리젠츠 오브 더 유니버시티 오브 미시간 | 개방된 금속 사이트를 지닌 미세 다공성 금속-유기골격구조에서의 높은 기체 흡착 |
| WO2007038508A2 (en) | 2005-09-26 | 2007-04-05 | The Regents Of The University Of Michigan | Metal-organic frameworks with exceptionally high capacity for storage of carbon dioxide at room-temperature |
| PL1988996T3 (pl) | 2006-02-28 | 2018-01-31 | Univ Michigan Regents | Otrzymywanie szkieletów zeolitu z grupami funkcyjnymi |
| US20080036003A1 (en) * | 2006-08-09 | 2008-02-14 | Goda Technology Co., Ltd. | Backlighted membrane switch |
| EP2103604A1 (de) | 2008-03-17 | 2009-09-23 | Evonik Degussa GmbH | Verfahren zur Herstellung von Epichlorhydrin |
| 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 |
| US8124797B2 (en) * | 2009-06-26 | 2012-02-28 | Lyondell Chemical Technology, Lp | Epoxidation process |
| CN102442980B (zh) * | 2010-10-11 | 2014-08-13 | 中国石油化工股份有限公司 | 环氧丙烷粗产品的精制方法和环氧丙烷的制备方法 |
| CN102442979B (zh) * | 2010-10-11 | 2014-10-08 | 中国石油化工股份有限公司 | 一种环氧丙烷的制备方法 |
| CN103172486B (zh) * | 2011-12-22 | 2015-07-29 | 中国石油化工股份有限公司 | 一种从直接环氧化反应产物中回收丙烯的方法 |
| PL3174866T3 (pl) | 2014-07-29 | 2020-06-29 | Evonik Operations Gmbh | Sposób epoksydowania olefiny |
| CN105585542B (zh) * | 2014-10-23 | 2018-09-28 | 中国石油化工股份有限公司 | 一种分离环氧氯丙烷的方法 |
| US10508032B2 (en) | 2015-03-20 | 2019-12-17 | Northwestern University | Catalysts and related methods for photocatalytic production of H2O2 and thermocatalytic reactant oxidation |
| WO2016173887A1 (en) | 2015-04-28 | 2016-11-03 | Evonik Degussa Gmbh | Process for the epoxidation of propene |
| US11402623B2 (en) | 2017-08-02 | 2022-08-02 | Corning Incorporated | Flexible subtrate and circuit for liquid lens system |
| CN113512013B (zh) * | 2021-06-30 | 2023-09-05 | 中国石油化工股份有限公司 | 一种大规模工业化甲醇制环氧丙烷的系统及方法 |
Family Cites Families (9)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US5028246A (en) * | 1986-02-03 | 1991-07-02 | Ensign-Bickford Optical Technologies, Inc. | Methods of making optical waveguides |
| US5006206A (en) * | 1990-03-12 | 1991-04-09 | Arco Chemical Technology, Inc. | Propylene oxide purification |
| US5107002A (en) | 1990-12-06 | 1992-04-21 | Arco Chemical Technology, L.P. | Lower alkylene oxide purification |
| US5133839A (en) * | 1991-07-25 | 1992-07-28 | Arco Chemical Technology, L.P. | Lower alkylene oxide purification |
| US5139622A (en) * | 1991-10-03 | 1992-08-18 | Texaco Chemical Company | Purification of propylene oxide by extractive distillation |
| US5354430A (en) | 1993-10-26 | 1994-10-11 | Texaco Chemical Company | Staged purification of contaminated propylene oxide |
| US5468885A (en) * | 1993-12-20 | 1995-11-21 | Arco Chemical Technology, L.P. | Epoxidizer oxygen recovery |
| DE19835907A1 (de) | 1998-08-07 | 2000-02-17 | Basf Ag | Verfahren zur Umsetzung einer organischen Verbindung mit einem Hydroperoxid |
| DE10015246A1 (de) | 2000-03-28 | 2001-10-04 | Basf Ag | Verfahren zur Umsetzung einer organischen Verbindung mit einem Hydroperoxid |
-
2000
- 2000-07-06 DE DE10032884A patent/DE10032884A1/de not_active Withdrawn
-
2001
- 2001-07-05 CN CNB018135773A patent/CN1230427C/zh not_active Expired - Fee Related
- 2001-07-05 MX MXPA03000017 patent/MX237891B/es active IP Right Grant
- 2001-07-05 DE DE50104409T patent/DE50104409D1/de not_active Revoked
- 2001-07-05 BR BR0112218-5A patent/BR0112218A/pt not_active IP Right Cessation
- 2001-07-05 MY MYPI20013201 patent/MY126819A/en unknown
- 2001-07-05 WO PCT/EP2001/007716 patent/WO2002002544A1/de active IP Right Grant
- 2001-07-05 AT AT01969340T patent/ATE281442T1/de not_active IP Right Cessation
- 2001-07-05 EP EP01969340A patent/EP1296968B1/de not_active Revoked
- 2001-07-05 CA CA002414756A patent/CA2414756A1/en not_active Abandoned
- 2001-07-05 RU RU2003103590/04A patent/RU2277089C2/ru not_active IP Right Cessation
- 2001-07-05 AU AU2001289624A patent/AU2001289624A1/en not_active Abandoned
- 2001-07-05 US US10/312,862 patent/US6756503B2/en not_active Expired - Lifetime
- 2001-07-06 TW TW090116609A patent/TW583181B/zh not_active IP Right Cessation
- 2001-09-12 SA SA01220361A patent/SA01220361B1/ar unknown
-
2003
- 2003-01-03 IN IN17CH2003 patent/IN2003CH00017A/en unknown
- 2003-01-06 ZA ZA200300106A patent/ZA200300106B/en unknown
Also Published As
| Publication number | Publication date |
|---|---|
| MY126819A (en) | 2006-10-31 |
| RU2277089C2 (ru) | 2006-05-27 |
| WO2002002544A1 (de) | 2002-01-10 |
| DE10032884A1 (de) | 2002-01-24 |
| TW583181B (en) | 2004-04-11 |
| ATE281442T1 (de) | 2004-11-15 |
| IN2003CH00017A (zh) | 2005-04-08 |
| SA01220361B1 (ar) | 2006-10-29 |
| CA2414756A1 (en) | 2003-01-06 |
| DE50104409D1 (de) | 2004-12-09 |
| EP1296968A1 (de) | 2003-04-02 |
| CN1230427C (zh) | 2005-12-07 |
| EP1296968B1 (de) | 2004-11-03 |
| US20030144535A1 (en) | 2003-07-31 |
| BR0112218A (pt) | 2003-05-06 |
| US6756503B2 (en) | 2004-06-29 |
| MXPA03000017A (es) | 2003-09-25 |
| AU2001289624A1 (en) | 2002-01-14 |
| MX237891B (es) | 2006-06-20 |
| CN1444575A (zh) | 2003-09-24 |
Similar Documents
| Publication | Publication Date | Title |
|---|---|---|
| US6756503B2 (en) | Method for the production of propylene oxide | |
| US6849162B2 (en) | Method for the production of propylene oxide | |
| EP1841753B1 (en) | A process for the epoxidation of an olefin with improved energy balance | |
| US7527712B2 (en) | Method for the continuous purification by distillation of the solvent methanol, used in the synthesis of propylene oxide | |
| US6881853B2 (en) | Method for producing propylene oxide | |
| WO2004092150A1 (de) | Verfahren zur herstellung von propylenoxid | |
| US20040192946A1 (en) | Method for the production of propylene oxide | |
| CA2493273A1 (en) | Process for the continuously operated intermediate isolation of the oxirane formed in the coproduct-free oxirane synthesis by means of a dividing wall column | |
| ZA200400338B (en) | Method for producing propylene oxide |