CA2125073A1 - Reactor and continuous process to be carried out therewith for the preparation of ethylene glycol carbonate and propylene glycol carbonate - Google Patents
Reactor and continuous process to be carried out therewith for the preparation of ethylene glycol carbonate and propylene glycol carbonateInfo
- Publication number
- CA2125073A1 CA2125073A1 CA002125073A CA2125073A CA2125073A1 CA 2125073 A1 CA2125073 A1 CA 2125073A1 CA 002125073 A CA002125073 A CA 002125073A CA 2125073 A CA2125073 A CA 2125073A CA 2125073 A1 CA2125073 A1 CA 2125073A1
- Authority
- CA
- Canada
- Prior art keywords
- glycol carbonate
- reaction mixture
- egc
- pgc
- bubble column
- 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
Links
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D317/00—Heterocyclic compounds containing five-membered rings having two oxygen atoms as the only ring hetero atoms
- C07D317/08—Heterocyclic compounds containing five-membered rings having two oxygen atoms as the only ring hetero atoms having the hetero atoms in positions 1 and 3
- C07D317/10—Heterocyclic compounds containing five-membered rings having two oxygen atoms as the only ring hetero atoms having the hetero atoms in positions 1 and 3 not condensed with other rings
- C07D317/32—Heterocyclic compounds containing five-membered rings having two oxygen atoms as the only ring hetero atoms having the hetero atoms in positions 1 and 3 not condensed with other rings with hetero atoms or with carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals, directly attached to ring carbon atoms
- C07D317/34—Oxygen atoms
- C07D317/36—Alkylene carbonates; Substituted alkylene carbonates
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D317/00—Heterocyclic compounds containing five-membered rings having two oxygen atoms as the only ring hetero atoms
- C07D317/08—Heterocyclic compounds containing five-membered rings having two oxygen atoms as the only ring hetero atoms having the hetero atoms in positions 1 and 3
- C07D317/10—Heterocyclic compounds containing five-membered rings having two oxygen atoms as the only ring hetero atoms having the hetero atoms in positions 1 and 3 not condensed with other rings
- C07D317/32—Heterocyclic compounds containing five-membered rings having two oxygen atoms as the only ring hetero atoms having the hetero atoms in positions 1 and 3 not condensed with other rings with hetero atoms or with carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals, directly attached to ring carbon atoms
- C07D317/34—Oxygen atoms
- C07D317/36—Alkylene carbonates; Substituted alkylene carbonates
- C07D317/38—Ethylene carbonate
-
- 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
- Y02P20/141—Feedstock
Abstract
A bubble column reactor is described which is characterized by a slenderness ratio at a ratio of height to diameter of 2 to 50, a feed, at the bottom end of the bubble column, for the ethylene glycol carbonate (EGC) or propylene glycol carbonate (PGC) already present serving as reaction medium, one or more metering sites for the starting materials CO2 and ethylene oxide (EOX) or propylene oxide (POX) above the feed for the reaction medium, an outlet for the reaction mixture at the top end of the bubble column, a dividing apparatus connected thereto for the reaction mixture flowing off for dividing it into reaction mixture to be taken off and worked up on the one hand and reaction mixture to be recycled on the other hand and additionally a return line to the feed for the reaction mixture to be recycled. This bubble column reactor can be advantageously used in a process for the continuous preparation of EGC or PGC which is carried out in the temperature range from 100 to 200°C, in the pressure range from 5 to 200 bar and at a molar ratio of 1.01 to 1.5 mol of CO2 per mol of alkylene oxide in EGC or PGC
already present as reaction medium in an amount which is 7 to 350 times that of the newly formed EGC or PGC.
already present as reaction medium in an amount which is 7 to 350 times that of the newly formed EGC or PGC.
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
DEP4318893.1 | 1993-06-07 | ||
DE4318893A DE4318893A1 (en) | 1993-06-07 | 1993-06-07 | Reactor and thus to be carried out continuous process for the preparation of ethylene glycol or propylene glycol |
Publications (2)
Publication Number | Publication Date |
---|---|
CA2125073A1 true CA2125073A1 (en) | 1994-12-08 |
CA2125073C CA2125073C (en) | 2005-07-26 |
Family
ID=6489815
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
CA002125073A Expired - Fee Related CA2125073C (en) | 1993-06-07 | 1994-06-03 | Reactor and continuous process to be carried out therewith for the preparation of ethylene glycol carbonate and propylene glycol carbonate |
Country Status (6)
Country | Link |
---|---|
US (1) | US5508442A (en) |
EP (1) | EP0628553B1 (en) |
JP (1) | JPH06345699A (en) |
CA (1) | CA2125073C (en) |
DE (2) | DE4318893A1 (en) |
ES (1) | ES2121114T3 (en) |
Families Citing this family (21)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JP3781549B2 (en) * | 1998-03-19 | 2006-05-31 | 三菱化学株式会社 | Method for producing monoethylene glycol |
US6080897A (en) * | 1998-03-19 | 2000-06-27 | Mitsubishi Chemical Corporation | Method for producing monoethylene glycol |
EP1119561B1 (en) * | 1998-10-07 | 2003-04-16 | Huntsman Petrochemical Corporation | Process for the preparation of alkylene carbonate |
MY141209A (en) * | 2003-03-13 | 2010-03-31 | Chiyoda Corp | Method of manufacturing acetic acid |
PT1791800T (en) * | 2004-09-02 | 2018-02-02 | Grupo Petrotemex Sa De Cv | Optimized liquid-phase oxidation |
JP4738786B2 (en) * | 2004-10-01 | 2011-08-03 | 旭化成ケミカルズ株式会社 | Method for producing ethylene carbonate |
JP4673028B2 (en) * | 2004-10-04 | 2011-04-20 | 旭化成ケミカルズ株式会社 | Method for purifying ethylene carbonate |
KR100668043B1 (en) | 2005-06-14 | 2007-01-15 | 한국과학기술연구원 | Production method of ethylene carbonate using loop reactor |
TWI383976B (en) * | 2006-02-22 | 2013-02-01 | Shell Int Research | Process for the production of dialkyl carbonate and alkanediol |
TW200740749A (en) * | 2006-02-22 | 2007-11-01 | Shell Int Research | Process for the preparation of an alkanediol and a dialkyl carbonate |
TW200740731A (en) * | 2006-02-22 | 2007-11-01 | Shell Int Research | Process for the preparation of alkanediol |
TWI382979B (en) * | 2006-02-22 | 2013-01-21 | Shell Int Research | Process for the production of alkylene carbonate and use of alkylene carbonate thus produced in the manufacture of an alkane diol and a dialkyl carbonate |
TWI378087B (en) * | 2006-02-22 | 2012-12-01 | Shell Int Research | Process for the preparation of an alkanediol and a dialkyl carbonate |
TWI387584B (en) * | 2006-03-13 | 2013-03-01 | Shell Int Research | Process for the production of alkylene carbonate and use of alkylene carbonate thus produced in the manufacture of an alkane diol and a dialkyl carbonate |
KR101666784B1 (en) | 2008-10-20 | 2016-10-17 | 쉘 인터내셔날 리써취 마트샤피지 비.브이. | Process for removing an alkanol impurity from an organic carbonate stream |
SG178263A1 (en) | 2009-08-12 | 2012-03-29 | Shell Int Research | Process for removing an alkanol impurity from a dialkyl carbonate stream |
TWI473786B (en) | 2009-11-16 | 2015-02-21 | Shell Int Research | Process for preparing alkanediol and dialkyl carbonate |
DE102010042937A1 (en) | 2010-10-08 | 2012-04-12 | Bayer Materialscience Aktiengesellschaft | Process for the preparation of diaryl carbonates from dialkyl carbonates |
EP2872481B1 (en) | 2012-07-11 | 2016-08-24 | Covestro Deutschland AG | Method for working up distillation residues from isocyanate production |
KR102505184B1 (en) * | 2019-08-21 | 2023-03-02 | 주식회사 엘지화학 | Preparation method of polyalkylene carbonate |
WO2021110627A1 (en) | 2019-12-06 | 2021-06-10 | Shell Internationale Research Maatschappij B.V. | Process for removing an ether alkanol impurity from an organic carbonate stream |
Family Cites Families (8)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
SU172342A (en) * | ||||
US4314945A (en) | 1977-12-22 | 1982-02-09 | Union Carbide Corporation | Alkylene carbonate process |
RO76854A2 (en) * | 1979-03-06 | 1981-08-30 | Centrala Industriala De Fire Si Fibre Sintetice,Ro | THERMOSTATED REACTOR FOR SYNTHESIS OF ETHYL CARBONATE |
JPS6059218B2 (en) * | 1980-12-23 | 1985-12-24 | 株式会社日本触媒 | Method for producing alkylene glycol |
DE3736988C1 (en) | 1987-10-31 | 1989-03-23 | Bayer Ag | Process for the continuous production of organic mono- and polyisocyanates |
DE3744001C1 (en) | 1987-12-24 | 1989-06-08 | Bayer Ag | Process for the continuous production of mono- or polyisocyanates |
DE4210943A1 (en) | 1992-04-02 | 1993-10-07 | Bayer Ag | Alkylene carbonate prepn., used for synthetic prodn. |
DE4141189A1 (en) * | 1991-12-13 | 1993-06-17 | Bayer Ag | METHOD FOR PRODUCING ETHYLENE GLYCOL CARBONATE |
-
1993
- 1993-06-07 DE DE4318893A patent/DE4318893A1/en not_active Withdrawn
-
1994
- 1994-05-25 EP EP94108037A patent/EP0628553B1/en not_active Expired - Lifetime
- 1994-05-25 DE DE59406801T patent/DE59406801D1/en not_active Expired - Fee Related
- 1994-05-25 ES ES94108037T patent/ES2121114T3/en not_active Expired - Lifetime
- 1994-05-31 US US08/251,229 patent/US5508442A/en not_active Expired - Lifetime
- 1994-06-03 CA CA002125073A patent/CA2125073C/en not_active Expired - Fee Related
- 1994-06-06 JP JP6145809A patent/JPH06345699A/en active Pending
Also Published As
Publication number | Publication date |
---|---|
JPH06345699A (en) | 1994-12-20 |
DE59406801D1 (en) | 1998-10-08 |
EP0628553A1 (en) | 1994-12-14 |
US5508442A (en) | 1996-04-16 |
CA2125073C (en) | 2005-07-26 |
EP0628553B1 (en) | 1998-09-02 |
DE4318893A1 (en) | 1994-12-08 |
ES2121114T3 (en) | 1998-11-16 |
Similar Documents
Publication | Publication Date | Title |
---|---|---|
CA2125073A1 (en) | Reactor and continuous process to be carried out therewith for the preparation of ethylene glycol carbonate and propylene glycol carbonate | |
IL47058A (en) | Distillation column reactor and process for carrying out reaction therein | |
EP1086940A4 (en) | Process for continuous production of dialkyl carbonate and diol | |
EP1174406A4 (en) | Process for continuously producing dialkyl carbonate and diol | |
CN103936591B (en) | The renovation process of methyl nitrite | |
JPS5592326A (en) | Simultaneous manufacture of pure methyllterttbutylether and c44hydrocarbon mixture scarecely containing isobutene | |
US4465852A (en) | Process for the production of carboxylic acid esters | |
EP0257435A3 (en) | Novel boron trifluoride-poly(alkylene oxide) amine catalysts for curing epoxy resins | |
RU2162862C2 (en) | Method of preparing polyetherpolyols with two terminal hydroxyl groups | |
CN102372610A (en) | Extraction and rectification technology and preparation apparatus of high-density methylal | |
MY132756A (en) | Pure ethylene oxide distillation process | |
JPH0458495B2 (en) | ||
US6160185A (en) | Process for purification of methylal | |
CN101121640A (en) | Method for producing ethylene glycol by catalysis rectification | |
CN102844292B (en) | Process for preparing carboxylic esters by reactive distillation | |
CN110759817B (en) | Preparation method of ethylene glycol mono-tert-butyl ether | |
CA2125075A1 (en) | Process for the preparation of propylene glycol carbonate | |
JPS5564579A (en) | Preparation of ethylene oxide | |
JPS57159806A (en) | Polymerization of olefin | |
GB1334100A (en) | Production of monothioalkylene glycols | |
CN111848889B (en) | Method for preparing polyformaldehyde by coproduction of trioxymethylene and dioxygen pentacyclic compound | |
CN103613504B (en) | Be the method that methylcarbonate prepared by raw material with carbonic acid third (second) alkene ester and methyl alcohol | |
JPS57183784A (en) | Preparation of organic carbonate | |
RU2036919C1 (en) | Method of 1,3-dioxolane synthesis | |
JPS55111259A (en) | Production of printing plate |
Legal Events
Date | Code | Title | Description |
---|---|---|---|
EEER | Examination request | ||
MKLA | Lapsed |