ES2149227T3 - Procedimiento para la obtencion de carbonato de propilenglicol. - Google Patents

Procedimiento para la obtencion de carbonato de propilenglicol.

Info

Publication number
ES2149227T3
ES2149227T3 ES94108038T ES94108038T ES2149227T3 ES 2149227 T3 ES2149227 T3 ES 2149227T3 ES 94108038 T ES94108038 T ES 94108038T ES 94108038 T ES94108038 T ES 94108038T ES 2149227 T3 ES2149227 T3 ES 2149227T3
Authority
ES
Spain
Prior art keywords
pgc
reactor
propylene glycol
reaction
procedure
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.)
Expired - Lifetime
Application number
ES94108038T
Other languages
English (en)
Inventor
Paul Dr Wagner
Christine Dr Mendoza-Frohn
Hans-Josef Dr Buysch
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
Bayer AG
Original Assignee
Bayer AG
Priority date (The priority date 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 date listed.)
Filing date
Publication date
Application filed by Bayer AG filed Critical Bayer AG
Application granted granted Critical
Publication of ES2149227T3 publication Critical patent/ES2149227T3/es
Anticipated expiration legal-status Critical
Expired - Lifetime legal-status Critical Current

Links

Classifications

    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D317/00Heterocyclic compounds containing five-membered rings having two oxygen atoms as the only ring hetero atoms
    • C07D317/08Heterocyclic compounds containing five-membered rings having two oxygen atoms as the only ring hetero atoms having the hetero atoms in positions 1 and 3
    • C07D317/10Heterocyclic 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
    • C07D317/32Heterocyclic 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
    • C07D317/34Oxygen atoms
    • C07D317/36Alkylene carbonates; Substituted alkylene carbonates
    • YGENERAL 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
    • Y02TECHNOLOGIES OR APPLICATIONS FOR MITIGATION OR ADAPTATION AGAINST CLIMATE CHANGE
    • Y02PCLIMATE CHANGE MITIGATION TECHNOLOGIES IN THE PRODUCTION OR PROCESSING OF GOODS
    • Y02P20/00Technologies relating to chemical industry
    • Y02P20/141Feedstock

Landscapes

  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
  • Low-Molecular Organic Synthesis Reactions Using Catalysts (AREA)

Abstract

SE DESCRIBE UN PROCESO PARA LA ELABORACION CATALITICA DE CARBONATO PROPILENGLICOL (PGC) MEDIANTE TRANSFORMACION DE OXIDO DE PROPILENO (POX) Y CO2 EN PGC COMO MEDIO DE REACCION EN TEMPERATURA ELEVADA Y PRESION ELEVADA, CON SEPARACION DEL PGC FORMADO DEL CATALIZADOR. EL PROCESO SE REALIZA DE FORMA CONTINUA MEDIANTE GUIA DE TEMPERATURA ADIABATICA. POR CADA UNIDAD DE TIEMPO SE DESARROLLA EL PGC COMO MEDIO DE REACCION EN EL REACTOR EN UNA RELACION DESDE 7 HASTA 350 VECES LA CANTIDAD DE PGC FORMADO POR UNIDAD DE TIEMPO. EN TODOS LOS LUGARES DEL REACTOR SE MANTIENE EL SOBRANTE CO2 SOBRE LOS OTROS PARTICIPANTES POX. A PARTIR DE LA MEZCLA DE REACCION DE DESARROLLO SE REALIZAN DESDE 80 HASTA 98 % EN PESO EN LA ENTRADA DEL REACTOR, MIENTRAS SE ELABORA SOBRE LA BASE PGC. PARA LA ELABORACION PUEDE SER UTILIZADA LA GUIA DE TEMPERATURA ADIABATICA DEL CALOR GENERADO DEL PRODUCTO DE REACCION.
ES94108038T 1993-06-07 1994-05-25 Procedimiento para la obtencion de carbonato de propilenglicol. Expired - Lifetime ES2149227T3 (es)

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
DE4318892A DE4318892A1 (de) 1993-06-07 1993-06-07 Verfahren zur Herstellung von Propylenglykolcarbonat

Publications (1)

Publication Number Publication Date
ES2149227T3 true ES2149227T3 (es) 2000-11-01

Family

ID=6489814

Family Applications (1)

Application Number Title Priority Date Filing Date
ES94108038T Expired - Lifetime ES2149227T3 (es) 1993-06-07 1994-05-25 Procedimiento para la obtencion de carbonato de propilenglicol.

Country Status (6)

Country Link
US (1) US5449791A (es)
EP (1) EP0628554B1 (es)
JP (1) JP3583473B2 (es)
CA (1) CA2125075C (es)
DE (2) DE4318892A1 (es)
ES (1) ES2149227T3 (es)

Families Citing this family (8)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN100393711C (zh) * 2003-06-04 2008-06-11 旭化成化学株式会社 生产碳酸亚烃酯的方法
TWI382979B (zh) * 2006-02-22 2013-01-21 Shell Int Research 碳酸伸烷酯之生產方法及由此生產的碳酸伸烷酯於烷二醇及碳酸二烷酯之製造中的用途
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
TWI383976B (zh) * 2006-02-22 2013-02-01 Shell Int Research 製備碳酸二烷酯及烷二醇的方法
TWI378087B (en) * 2006-02-22 2012-12-01 Shell Int Research Process for the preparation of an alkanediol and a dialkyl carbonate
TWI387584B (zh) * 2006-03-13 2013-03-01 Shell Int Research 碳酸伸烷酯之生產方法及由此生產之碳酸伸烷酯於烷二醇及碳酸二烷酯之製造中之用途
ES2356278T3 (es) * 2007-04-23 2011-04-06 Shell Internationale Research Maatschappij B.V. Procedimiento para preparar un carbonato de 1,2-alquileno.

Family Cites Families (9)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
SU172342A (es) *
US4314945A (en) * 1977-12-22 1982-02-09 Union Carbide Corporation Alkylene carbonate process
US4247465A (en) * 1979-08-23 1981-01-27 Atlantic Richfield Company Preparation of alkylene carbonates from olefins
JPS6059218B2 (ja) * 1980-12-23 1985-12-24 株式会社日本触媒 アルキレングリコ−ルの製造方法
DE3736988C1 (de) * 1987-10-31 1989-03-23 Bayer Ag Verfahren zur kontinuierlichen Herstellung von organischen Mono- und Polyisocyanaten
DE4028708A1 (de) * 1990-09-10 1992-03-12 Huels Chemische Werke Ag Verfahren zur herstellung von hochreinem propylencarbonat und zur gleichzeitigen herstellung von passivierten elektroden
DE4129753C2 (de) * 1991-09-04 1995-05-04 Dainippon Ink & Chemicals Verfahren zur Herstellung von Cyclocarbonatverbindungen
DE4141189A1 (de) * 1991-12-13 1993-06-17 Bayer Ag Verfahren zur herstellung von ethylenglykolcarbonat
US5281723A (en) * 1992-08-04 1994-01-25 International Business Machines Propylene carbonate recovery process

Also Published As

Publication number Publication date
US5449791A (en) 1995-09-12
JPH06345698A (ja) 1994-12-20
CA2125075A1 (en) 1994-12-08
DE59409466D1 (de) 2000-09-07
JP3583473B2 (ja) 2004-11-04
CA2125075C (en) 2005-08-16
EP0628554B1 (de) 2000-08-02
DE4318892A1 (de) 1994-12-08
EP0628554A1 (de) 1994-12-14

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