SA99191303B1 - طريقة لصنع اوكسيرين - Google Patents
طريقة لصنع اوكسيرين Download PDFInfo
- Publication number
- SA99191303B1 SA99191303B1 SA99191303A SA99191303A SA99191303B1 SA 99191303 B1 SA99191303 B1 SA 99191303B1 SA 99191303 A SA99191303 A SA 99191303A SA 99191303 A SA99191303 A SA 99191303A SA 99191303 B1 SA99191303 B1 SA 99191303B1
- Authority
- SA
- Saudi Arabia
- Prior art keywords
- peroxide
- process according
- solvent
- reaction medium
- catalyst
- Prior art date
Links
- IAYPIBMASNFSPL-UHFFFAOYSA-N Ethylene oxide Chemical compound C1CO1 IAYPIBMASNFSPL-UHFFFAOYSA-N 0.000 title description 3
- 238000000034 method Methods 0.000 claims abstract description 28
- 239000003054 catalyst Substances 0.000 claims abstract description 23
- -1 peroxide compound Chemical class 0.000 claims abstract description 21
- 239000012429 reaction media Substances 0.000 claims abstract description 15
- 239000002904 solvent Substances 0.000 claims abstract description 13
- 239000010457 zeolite Substances 0.000 claims abstract description 13
- 229910021536 Zeolite Inorganic materials 0.000 claims abstract description 11
- HNPSIPDUKPIQMN-UHFFFAOYSA-N dioxosilane;oxo(oxoalumanyloxy)alumane Chemical compound O=[Si]=O.O=[Al]O[Al]=O HNPSIPDUKPIQMN-UHFFFAOYSA-N 0.000 claims abstract description 10
- MHAJPDPJQMAIIY-UHFFFAOYSA-N Hydrogen peroxide Chemical group OO MHAJPDPJQMAIIY-UHFFFAOYSA-N 0.000 claims description 22
- 238000006243 chemical reaction Methods 0.000 claims description 15
- OKKJLVBELUTLKV-UHFFFAOYSA-N Methanol Chemical compound OC OKKJLVBELUTLKV-UHFFFAOYSA-N 0.000 claims description 12
- 150000002978 peroxides Chemical class 0.000 claims description 9
- QQONPFPTGQHPMA-UHFFFAOYSA-N propylene Natural products CC=C QQONPFPTGQHPMA-UHFFFAOYSA-N 0.000 claims description 7
- GOOHAUXETOMSMM-UHFFFAOYSA-N Propylene oxide Chemical compound CC1CO1 GOOHAUXETOMSMM-UHFFFAOYSA-N 0.000 claims description 6
- 125000004805 propylene group Chemical group [H]C([H])([H])C([H])([*:1])C([H])([H])[*:2] 0.000 claims description 6
- VMHLLURERBWHNL-UHFFFAOYSA-M Sodium acetate Chemical group [Na+].CC([O-])=O VMHLLURERBWHNL-UHFFFAOYSA-M 0.000 claims description 3
- RTAQQCXQSZGOHL-UHFFFAOYSA-N Titanium Chemical compound [Ti] RTAQQCXQSZGOHL-UHFFFAOYSA-N 0.000 claims description 3
- 239000001632 sodium acetate Substances 0.000 claims description 3
- 235000017281 sodium acetate Nutrition 0.000 claims description 3
- 239000010936 titanium Substances 0.000 claims description 3
- 229910052719 titanium Inorganic materials 0.000 claims description 3
- 150000001875 compounds Chemical class 0.000 claims description 2
- 239000013078 crystal Substances 0.000 claims description 2
- 239000002245 particle Substances 0.000 claims description 2
- QTBSBXVTEAMEQO-UHFFFAOYSA-M Acetate Chemical compound CC([O-])=O QTBSBXVTEAMEQO-UHFFFAOYSA-M 0.000 claims 1
- DGAQECJNVWCQMB-PUAWFVPOSA-M Ilexoside XXIX Chemical compound C[C@@H]1CC[C@@]2(CC[C@@]3(C(=CC[C@H]4[C@]3(CC[C@@H]5[C@@]4(CC[C@@H](C5(C)C)OS(=O)(=O)[O-])C)C)[C@@H]2[C@]1(C)O)C)C(=O)O[C@H]6[C@@H]([C@H]([C@@H]([C@H](O6)CO)O)O)O.[Na+] DGAQECJNVWCQMB-PUAWFVPOSA-M 0.000 claims 1
- BPQQTUXANYXVAA-UHFFFAOYSA-N Orthosilicate Chemical compound [O-][Si]([O-])([O-])[O-] BPQQTUXANYXVAA-UHFFFAOYSA-N 0.000 claims 1
- ABRVLXLNVJHDRQ-UHFFFAOYSA-N [2-pyridin-3-yl-6-(trifluoromethyl)pyridin-4-yl]methanamine Chemical compound FC(C1=CC(=CC(=N1)C=1C=NC=CC=1)CN)(F)F ABRVLXLNVJHDRQ-UHFFFAOYSA-N 0.000 claims 1
- 230000001681 protective effect Effects 0.000 claims 1
- 229910052708 sodium Inorganic materials 0.000 claims 1
- 239000011734 sodium Substances 0.000 claims 1
- 150000001336 alkenes Chemical class 0.000 abstract description 11
- JRZJOMJEPLMPRA-UHFFFAOYSA-N olefin Natural products CCCCCCCC=C JRZJOMJEPLMPRA-UHFFFAOYSA-N 0.000 abstract description 10
- 150000002118 epoxides Chemical class 0.000 abstract 2
- 150000002924 oxiranes Chemical class 0.000 description 13
- 239000002585 base Substances 0.000 description 7
- 125000004432 carbon atom Chemical group C* 0.000 description 4
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 description 3
- HEMHJVSKTPXQMS-UHFFFAOYSA-M Sodium hydroxide Chemical compound [OH-].[Na+] HEMHJVSKTPXQMS-UHFFFAOYSA-M 0.000 description 3
- 239000007864 aqueous solution Substances 0.000 description 3
- 239000000463 material Substances 0.000 description 3
- 239000000047 product Substances 0.000 description 3
- KWYUFKZDYYNOTN-UHFFFAOYSA-M Potassium hydroxide Chemical compound [OH-].[K+] KWYUFKZDYYNOTN-UHFFFAOYSA-M 0.000 description 2
- 150000007529 inorganic bases Chemical class 0.000 description 2
- 150000007530 organic bases Chemical class 0.000 description 2
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 2
- 101100497235 Bacillus thuringiensis subsp. kenyae cry1Ea gene Proteins 0.000 description 1
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 description 1
- 238000010521 absorption reaction Methods 0.000 description 1
- 239000002253 acid Substances 0.000 description 1
- 150000007513 acids Chemical class 0.000 description 1
- 125000001931 aliphatic group Chemical group 0.000 description 1
- 229910052783 alkali metal Inorganic materials 0.000 description 1
- 150000001340 alkali metals Chemical class 0.000 description 1
- 125000000217 alkyl group Chemical group 0.000 description 1
- 239000004411 aluminium Substances 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
- QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical compound [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 description 1
- 239000006227 byproduct Substances 0.000 description 1
- 229910052799 carbon Inorganic materials 0.000 description 1
- 150000001735 carboxylic acids Chemical class 0.000 description 1
- 238000002474 experimental method Methods 0.000 description 1
- 229910052739 hydrogen Inorganic materials 0.000 description 1
- 239000001257 hydrogen Substances 0.000 description 1
- XASUTLWDRZFPII-UHFFFAOYSA-N hydrogen peroxide;prop-1-ene Chemical compound OO.CC=C XASUTLWDRZFPII-UHFFFAOYSA-N 0.000 description 1
- 229910052500 inorganic mineral Inorganic materials 0.000 description 1
- 239000011707 mineral Substances 0.000 description 1
- 239000000203 mixture Substances 0.000 description 1
- 150000002894 organic compounds Chemical class 0.000 description 1
- 229910052760 oxygen Inorganic materials 0.000 description 1
- 239000001301 oxygen Substances 0.000 description 1
- 239000011148 porous material Substances 0.000 description 1
- 125000001453 quaternary ammonium group Chemical group 0.000 description 1
- 238000004064 recycling Methods 0.000 description 1
- 150000003839 salts Chemical class 0.000 description 1
- 239000000377 silicon dioxide Substances 0.000 description 1
- 239000007787 solid Substances 0.000 description 1
- 239000000126 substance Substances 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
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B01—PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
- B01J—CHEMICAL OR PHYSICAL PROCESSES, e.g. CATALYSIS OR COLLOID CHEMISTRY; THEIR RELEVANT APPARATUS
- B01J29/00—Catalysts comprising molecular sieves
- B01J29/89—Silicates, aluminosilicates or borosilicates of titanium, zirconium or hafnium
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D303/00—Compounds containing three-membered rings having one oxygen atom as the only ring hetero atom
- C07D303/02—Compounds containing oxirane rings
- C07D303/04—Compounds containing oxirane rings containing only hydrogen and carbon atoms in addition to the ring oxygen atoms
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Inorganic Chemistry (AREA)
- Engineering & Computer Science (AREA)
- Materials Engineering (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Epoxy Compounds (AREA)
- Low-Molecular Organic Synthesis Reactions Using Catalysts (AREA)
- Catalysts (AREA)
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| BE9800231A BE1011851A3 (fr) | 1998-03-24 | 1998-03-24 | Procede de fabrication d'un oxiranne. |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| SA99191303B1 true SA99191303B1 (ar) | 2006-08-14 |
Family
ID=3891170
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| SA99191303A SA99191303B1 (ar) | 1998-03-24 | 1999-04-14 | طريقة لصنع اوكسيرين |
Country Status (22)
| Country | Link |
|---|---|
| US (1) | US6429322B1 (enExample) |
| EP (1) | EP1066274B1 (enExample) |
| JP (1) | JP2002507607A (enExample) |
| KR (1) | KR100572805B1 (enExample) |
| CN (1) | CN1330642C (enExample) |
| AR (1) | AR018802A1 (enExample) |
| AT (1) | ATE277028T1 (enExample) |
| AU (1) | AU3035999A (enExample) |
| BE (1) | BE1011851A3 (enExample) |
| BR (1) | BR9909047A (enExample) |
| CA (1) | CA2323005C (enExample) |
| DE (1) | DE69920420T2 (enExample) |
| ES (1) | ES2229689T3 (enExample) |
| HU (1) | HUP0102062A2 (enExample) |
| ID (1) | ID27494A (enExample) |
| NO (1) | NO20004739L (enExample) |
| PL (1) | PL197387B1 (enExample) |
| SA (1) | SA99191303B1 (enExample) |
| SK (1) | SK14232000A3 (enExample) |
| TW (1) | TW539673B (enExample) |
| WO (1) | WO1999048882A1 (enExample) |
| ZA (1) | ZA200004995B (enExample) |
Families Citing this family (19)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| IT1313572B1 (it) | 1999-07-27 | 2002-09-09 | Enichem Spa | Procedimento per la preparazione di epossidi. |
| DE19944839A1 (de) | 1999-09-18 | 2001-03-22 | Degussa | Verfahren zur Herstellung von Epoxiden aus Olefinen |
| FR2810982B1 (fr) | 2000-06-28 | 2002-09-27 | Solvay | Procede de fabrication d'oxiranne comprenant la separation de l'oxiranne du milieu reactionnel |
| FR2810980B1 (fr) | 2000-06-28 | 2004-05-21 | Solvay | Procede de fabrication d'oxiranne en presence d'un catalyseur sous forme de particules |
| FR2810983B1 (fr) | 2000-06-28 | 2004-05-21 | Solvay | Procede de fabrication d'oxiranne au moyen d'un compose peroxyde |
| FR2824558B1 (fr) * | 2001-05-14 | 2005-05-06 | Solvay | Procede de fabrication d'un oxiranne |
| US7722847B2 (en) * | 2002-09-30 | 2010-05-25 | Evonik Degussa Gmbh | Aqueous hydrogen peroxide solutions and method of making same |
| EP1403259A1 (en) * | 2002-09-30 | 2004-03-31 | Degussa AG | Process for the epoxidation of olefins |
| US6838572B2 (en) * | 2002-09-30 | 2005-01-04 | Degussa Ag | Process for the epoxidation of olefins |
| 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 |
| CN101687639B (zh) | 2007-04-05 | 2015-04-29 | 索尔维公司 | 水性过氧化氢溶液、它的制备方法及其用途 |
| EP2501687B1 (en) | 2009-11-19 | 2014-10-15 | Dow Global Technologies LLC | Epoxidation of an olefin |
| RU2588575C2 (ru) | 2010-12-07 | 2016-07-10 | Басф Се | Способ получения пропиленоксида |
| US8785670B2 (en) | 2010-12-07 | 2014-07-22 | Basf Se | Process for the production of propylene oxide |
| CN103347868A (zh) | 2011-01-27 | 2013-10-09 | 索尔维公司 | 用于制造1，2-环氧-3-氯丙烷的方法 |
| EA201391089A1 (ru) | 2011-01-27 | 2014-06-30 | Солвей Са | Способ изготовления 1,2-эпокси-3-хлорпропана |
| CN103172597B (zh) * | 2013-04-03 | 2017-12-22 | 北京石油化工学院 | 钛硅分子筛催化合成环氧脂肪酸甲酯的方法 |
| CN107325072A (zh) * | 2017-07-05 | 2017-11-07 | 中国石油化工股份有限公司 | 一种合成环碳酸辛烯酯的方法 |
Family Cites Families (4)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| EP0230949B1 (en) * | 1986-01-28 | 1992-07-22 | ENIRICERCHE S.p.A. | A process for the epoxydation of olefinic compounds |
| US5646314A (en) * | 1994-11-16 | 1997-07-08 | Arco Chemical Technology, L.P. | Process for titanium silicalite-catalyzed epoxidation |
| DE19528219A1 (de) * | 1995-08-01 | 1997-02-06 | Degussa | Verfahren zur Herstellung von Epoxiden aus Olefinen |
| IT1283232B1 (it) * | 1996-03-12 | 1998-04-16 | Enichem Spa | Procedimento per la sintesi di 2-buten-1, 4-diesteri |
-
1998
- 1998-03-24 BE BE9800231A patent/BE1011851A3/fr not_active IP Right Cessation
-
1999
- 1999-03-19 TW TW088104345A patent/TW539673B/zh not_active IP Right Cessation
- 1999-03-20 ID IDW20002161A patent/ID27494A/id unknown
- 1999-03-20 JP JP2000537865A patent/JP2002507607A/ja active Pending
- 1999-03-20 CA CA002323005A patent/CA2323005C/fr not_active Expired - Lifetime
- 1999-03-20 PL PL343067A patent/PL197387B1/pl unknown
- 1999-03-20 BR BR9909047-3A patent/BR9909047A/pt not_active Application Discontinuation
- 1999-03-20 HU HU0102062A patent/HUP0102062A2/hu unknown
- 1999-03-20 CN CNB998043648A patent/CN1330642C/zh not_active Expired - Lifetime
- 1999-03-20 KR KR1020007010443A patent/KR100572805B1/ko not_active Expired - Lifetime
- 1999-03-20 WO PCT/EP1999/001955 patent/WO1999048882A1/fr not_active Ceased
- 1999-03-20 DE DE69920420T patent/DE69920420T2/de not_active Expired - Lifetime
- 1999-03-20 AU AU30359/99A patent/AU3035999A/en not_active Abandoned
- 1999-03-20 ES ES99911811T patent/ES2229689T3/es not_active Expired - Lifetime
- 1999-03-20 SK SK1423-2000A patent/SK14232000A3/sk unknown
- 1999-03-20 EP EP99911811A patent/EP1066274B1/fr not_active Revoked
- 1999-03-20 AT AT99911811T patent/ATE277028T1/de not_active IP Right Cessation
- 1999-03-23 AR ARP990101287A patent/AR018802A1/es unknown
- 1999-04-14 SA SA99191303A patent/SA99191303B1/ar unknown
- 1999-09-20 US US09/646,788 patent/US6429322B1/en not_active Expired - Lifetime
-
2000
- 2000-09-19 ZA ZA200004995A patent/ZA200004995B/en unknown
- 2000-09-22 NO NO20004739A patent/NO20004739L/no unknown
Also Published As
| Publication number | Publication date |
|---|---|
| NO20004739D0 (no) | 2000-09-22 |
| JP2002507607A (ja) | 2002-03-12 |
| PL343067A1 (en) | 2001-07-30 |
| DE69920420T2 (de) | 2005-11-17 |
| DE69920420D1 (de) | 2004-10-28 |
| CA2323005A1 (fr) | 1999-09-30 |
| PL197387B1 (pl) | 2008-03-31 |
| NO20004739L (no) | 2000-10-03 |
| WO1999048882A1 (fr) | 1999-09-30 |
| EP1066274B1 (fr) | 2004-09-22 |
| ID27494A (id) | 2001-04-12 |
| ATE277028T1 (de) | 2004-10-15 |
| BE1011851A3 (fr) | 2000-02-01 |
| ZA200004995B (en) | 2002-07-05 |
| BR9909047A (pt) | 2000-12-05 |
| CN1294586A (zh) | 2001-05-09 |
| AR018802A1 (es) | 2001-12-12 |
| EP1066274A1 (fr) | 2001-01-10 |
| AU3035999A (en) | 1999-10-18 |
| US6429322B1 (en) | 2002-08-06 |
| HUP0102062A2 (hu) | 2001-09-28 |
| TW539673B (en) | 2003-07-01 |
| KR20010042087A (ko) | 2001-05-25 |
| CA2323005C (fr) | 2009-02-24 |
| ES2229689T3 (es) | 2005-04-16 |
| SK14232000A3 (sk) | 2002-01-07 |
| CN1330642C (zh) | 2007-08-08 |
| KR100572805B1 (ko) | 2006-04-25 |
Similar Documents
| Publication | Publication Date | Title |
|---|---|---|
| EP0100119B1 (en) | Process for the epoxidation of olefinic compounds | |
| Saxton | Crystalline microporous titanium silicates | |
| KR100572805B1 (ko) | 에폭시드 제조방법 | |
| Khouw et al. | Catalytic activity of titanium silicates synthesized in the presence of alkali-metal and alkaline-earth ions | |
| US4824976A (en) | Process for the epoxidation of olefinic compounds and catalysts used therein | |
| US6380407B1 (en) | Method for making an oxirane | |
| US5621122A (en) | Epoxidation process | |
| US7323578B2 (en) | Process for manufacturing an oxirane | |
| RU2575936C2 (ru) | Катализатор и способ его получения и способ эпоксидирования олефина | |
| CA2319284A1 (en) | Process for the preparation of epoxides from olefins | |
| ITMI980053A1 (it) | Procedimento per la preparazione di epossidi olefinici | |
| Li et al. | Effect of sodium ions on propylene epoxidation catalyzed by titanium silicalite | |
| CN107376988B (zh) | 一种高活性的丙烯气相环氧化催化剂及其制备方法和应用 | |
| Gabelica et al. | Synthesis of MFI metallosilicate zeolites using metallic amino complexes as mineralizing agents: an overview | |
| JP2000506772A (ja) | 貴金属不含の触媒組成物 | |
| US6627175B2 (en) | Process for the manufacture of a crystalline solid | |
| JP2002507607A5 (enExample) | ||
| US20040039216A1 (en) | Oxirane production using peroxidized compound | |
| WO1997024286A1 (en) | Synthetic crystalline material comprising oxides of silicon and titanium | |
| ES2292811T3 (es) | Procedimiento de epoxidacion directa usando un sistema catalizador mixto. | |
| CA2219248A1 (en) | Process for the preparation of titanium-containing molecular sieves | |
| US7786318B2 (en) | Catalyst preparation | |
| CN110143905B (zh) | 制备过氧丙酸的方法 | |
| Wahlen et al. | Lanthanum-exchanged zeolites as active and selective catalysts for the generation of singlet oxygen from hydrogen peroxide | |
| CN108283934B (zh) | 环己烷氧化液加工的方法 |