ES250333A1 - Improvements in or relating to the preparation of a mixture of glycerol and glycols - Google Patents

Improvements in or relating to the preparation of a mixture of glycerol and glycols

Info

Publication number
ES250333A1
ES250333A1 ES0250333A ES250333A ES250333A1 ES 250333 A1 ES250333 A1 ES 250333A1 ES 0250333 A ES0250333 A ES 0250333A ES 250333 A ES250333 A ES 250333A ES 250333 A1 ES250333 A1 ES 250333A1
Authority
ES
Spain
Prior art keywords
glycerol
nickel
glycols
mixture
preparation
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
Application number
ES0250333A
Other languages
Spanish (es)
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.)
Inventa AG fuer Forschung und Patentverwertung
Original Assignee
Inventa AG fuer Forschung und Patentverwertung
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
Priority claimed from CH6155058A external-priority patent/CH373025A/en
Application filed by Inventa AG fuer Forschung und Patentverwertung filed Critical Inventa AG fuer Forschung und Patentverwertung
Publication of ES250333A1 publication Critical patent/ES250333A1/en
Expired legal-status Critical Current

Links

Classifications

    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07CACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C29/00Preparation of compounds having hydroxy or O-metal groups bound to a carbon atom not belonging to a six-membered aromatic ring

Abstract

A mixture of glycerol and glycols with less than 6 carbon atoms in the chain, is prepared in a one-stage process in which an aqueous solution of sucrose is catalytically hydrogenated at elevated temperature and pressure at a pH of from 11 to 12.5 at least at the beginning of the hydrogenation. A pH of 12 is preferred and is adjusted by alkali or alkaline earth metal hydroxide. The process may be continuous at between 180 and 250 DEG C. and 50 to 250 atmospheres pressure. Catalysts such as nickel or kieselguhr and aluminium oxide, Raney nickel, or nickel-magnesium oxalate and during the continuous process hydrogen saturated with steam may be used and the reaction product is concentrated from 10 to 40% weight by volume. Examples describe the preparation of mixtures containing pentitol, erythritol, glycerol, ethylene and propylene glycol, butanediol.
ES0250333A 1958-07-09 1959-06-25 Improvements in or relating to the preparation of a mixture of glycerol and glycols Expired ES250333A1 (en)

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
CH6155058A CH373025A (en) 1958-07-09 1958-07-09 Process for the production of glycerine and glycols
CH7284259A CH423738A (en) 1958-07-09 1959-05-02 Process for the production of glycerine and glycols

Publications (1)

Publication Number Publication Date
ES250333A1 true ES250333A1 (en) 1959-10-16

Family

ID=25737721

Family Applications (1)

Application Number Title Priority Date Filing Date
ES0250333A Expired ES250333A1 (en) 1958-07-09 1959-06-25 Improvements in or relating to the preparation of a mixture of glycerol and glycols

Country Status (3)

Country Link
CH (1) CH423738A (en)
ES (1) ES250333A1 (en)
GB (1) GB916774A (en)

Families Citing this family (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
DE2756270A1 (en) * 1977-12-16 1979-06-21 Bayer Ag METHOD FOR PRODUCING LOW MOLECULAR POLYHYDROXYL COMPOUNDS
CA2178733C (en) * 1993-12-29 1999-02-16 Pamela M. Mazurek Liquid sorbitol/mannitol/glycerin blend and compositions containing same

Also Published As

Publication number Publication date
CH423738A (en) 1966-11-15
GB916774A (en) 1963-01-30

Similar Documents

Publication Publication Date Title
GB976339A (en) Improvements in or relating to the production of cyclohexanone
JPS5424838A (en) Process for preparing 2*22dichloroohydrazobenzene
GB1045680A (en) Improvements relating to catalysts and their use
GB942963A (en) Purification of butynediol
ES250333A1 (en) Improvements in or relating to the preparation of a mixture of glycerol and glycols
GB899653A (en) Improvements relating to the hydrogenation of gasolines
GB1377192A (en) Hydrogenation process for the preparation of aliphatic diamines
GB858514A (en) Improvements in or relating to nitrile compounds, the preparation thereof and by-products of said preparation
GB1475486A (en) Process for the production of gamma-butyrolactone
US2300598A (en) Process of producing butene-2-diol-1, 4 and its substitution products
GB1318598A (en) Process for the production of saturated monocyclic monoterpenes
GB514693A (en) Improvements in and relating to the production of polyhydric alcohols
GB888045A (en) A process for the manufacture of lithium aluminium hydride
GB938346A (en) Hydrogenation of butyne-2-diol, 1, 4 to butene-2-diol, 1, 4
GB803373A (en) Dehydrogenation catalyst and a process for its production
FR2226388A1 (en) Epsilon-aminocaproamide prodn in liq. ammonia - by catalytic hydrogen-ation of epsilon -nitrocaproamide under pressure
GB820662A (en) Improvements relating to the production of polyhydric alcohols
GB1106088A (en) Process for the preparation of phloroglucinol
ES312946A1 (en) Procedure for the production of trans-4-aminomethylcyclohexan-1-carboxylic acid. (Machine-translation by Google Translate, not legally binding)
GB600426A (en) Improvements in or relating to the production of p-methyl-amino-phenol
GB736074A (en) Process for the manufacture of butyraldehyde
GB587181A (en) Improvement in catalytic hydrogenation of acetophenone to phenyl methyl carbinol
GB522729A (en) Improvements in the manufacture of mannitol
GB834771A (en) Improvements relating to the production of glycerol and glycols
GB648904A (en) Process for the manufacture of 2:4:5-triamino-6-hydroxy-pyrimidine