GB693981A - A process for isomerising unsaturated fatty acids or esters thereof - Google Patents

A process for isomerising unsaturated fatty acids or esters thereof

Info

Publication number
GB693981A
GB693981A GB19719/50A GB1971950A GB693981A GB 693981 A GB693981 A GB 693981A GB 19719/50 A GB19719/50 A GB 19719/50A GB 1971950 A GB1971950 A GB 1971950A GB 693981 A GB693981 A GB 693981A
Authority
GB
United Kingdom
Prior art keywords
oil
nickel
fatty acids
cobalt
linseed oil
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
GB19719/50A
Inventor
Johan Jacobus Albert Blekkingh
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.)
Unilever PLC
Lever Brothers and Unilever Ltd
Original Assignee
Unilever PLC
Lever Brothers and Unilever Ltd
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 Unilever PLC, Lever Brothers and Unilever Ltd filed Critical Unilever PLC
Publication of GB693981A publication Critical patent/GB693981A/en
Expired legal-status Critical Current

Links

Classifications

    • CCHEMISTRY; METALLURGY
    • C11ANIMAL OR VEGETABLE OILS, FATS, FATTY SUBSTANCES OR WAXES; FATTY ACIDS THEREFROM; DETERGENTS; CANDLES
    • C11CFATTY ACIDS FROM FATS, OILS OR WAXES; CANDLES; FATS, OILS OR FATTY ACIDS BY CHEMICAL MODIFICATION OF FATS, OILS, OR FATTY ACIDS OBTAINED THEREFROM
    • C11C3/00Fats, oils, or fatty acids by chemical modification of fats, oils, or fatty acids obtained therefrom
    • C11C3/14Fats, oils, or fatty acids by chemical modification of fats, oils, or fatty acids obtained therefrom by isomerisation

Landscapes

  • Chemical & Material Sciences (AREA)
  • General Chemical & Material Sciences (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Engineering & Computer Science (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Oil, Petroleum & Natural Gas (AREA)
  • Wood Science & Technology (AREA)
  • Organic Chemistry (AREA)
  • Fats And Perfumes (AREA)
  • Catalysts (AREA)

Abstract

Unsaturated fatty acids or their esters are isomerized by heating them to a temperature not exceeding 140 DEG C. in presence of a catalyst prepared by reduction of a nickel or cobalt compound and comprising nickel or cobalt, nickel or cobalt silicate and a proportion of sulphur not exceeding 10 per cent based on the weight of the metal. Thus oleic acid, linseed oil fatty acids, linseed oil itself, other fatty oils of the drying, semi-drying and non-drying types, and alkyl esters of unsaturated fatty acids, particularly the ethyl esters, may be isomerized by this method. As a result of the isomerization, cis-stereoisomers become converted to the corresponding trans-stereoisomers, while double bonds become conjugated. In the examples, a catalyst is prepared by boiling together nickel sulphate, diatomaceous earth, sodium carbonate and water, boiling the precipitate obtained with further nickel sulphate solution and finally reducing the precipitate with hydrogen; this catalyst is used to isomerize linseed oil, soyabean oil, sunflower seed oil, cottonseed oil, sesame oil, whale oil, teaseed oil, ground nut oil, palm oil, linseed oil fatty acids, methyl esters of linseed oil fatty acids and methyl oleate. In the case of linseed oil, the oil may be neutralized and bleached before isomerization, while in the case of linseed oil fatty acids, the isomerization may be followed by sulphuric acid treatment. The isomerization is conducted under an atmosphere of carbon dioxide and at various temperatures. Specifications 645,872 and 646,919, [both in Group III], are referred to.ALSO:Unsaturated fatty acids or their esters are isomerized by heating them to a temperature not exceeding 140 DEG C in presence of a catalyst prepared by reduction of a nickel or cobalt compound and comprising nickel or cobalt, nickel or cobalt silicate and a proportion of sulphur not exceeding 10 per cent based on the weight of the metal. Thus oleic acid, linseed oil fatty acids, linseed oil itself, other fatty oils of the dry, semi-drying and non-drying types, and alkyl esters of unsaturated fatty acids, particularly the ethyl esters, may be isomerized by this method. As a result of the isomerization, cisstereoisomers become converted to the corresponding trans - stereoisomers, while double bonds become conjugated. In the examples, a catalyst is prepared by boiling together nickel sulphate, diatomaceous earth, sodium carbonate and water, boiling the precipitate obtained with further nickel sulphate solution and finally reducing the precipitate with hydrogen; this catalyst is used to isomerize linseed oil, soyabean oil, sunflower seed oil, cottonseed oil, sesame oil, whale oil, teaseed oil, groundnut oil, palm oil, linseed oil fatty acids, methyl esters of linseed oil fatty acids and methyl oleate In the case of linseed oil, the oil may be neutralized and bleached before isomerization, while in the case of linseed oil fatty acids, the isomerization may be followed by sulphuric acid treatment. The isomerization is conducted under an atmosphere of carbon dioxide and at various temperatures. Specifications 645,872 and 646,919 are referred to. Preparation of catalysts. Nickel or cobalt may be precipitated in the form of an insoluble compound from a solution of the metal salt, for example nickel or cobalt sulphate, in the presence of a material capable of forming a silicate with part of the p precipitate, for example diatomaceous earth or waterglass. Alternatively, the catalyst may be prepared by boiling a precipitate of a compound of the metal, for example nickel or cobalt hydroxide, with a material such as diatomaceous earth or water glass in an alkaline aqueous solution and separating the precipitate. The separated precipitate formed by either method is then reduced in a current of hydrogen at a temperature at which metallic nickel or cobalt is formed, for example 500 DEG C. The sulphur content can be imparted by treating the precipitate formed with alkali with a solution of a sulphur-containing nickel or cobalt compound, for example nickel sulphate, or by mixing the filtered and dried precipitate with sulphur or a sulphur compound before reduction takes place. Alternatively, the sulphur content can be imparted by treating the reduced catalyst with hydrogen sulphide or by using the reduced catalyst to hydrogenate a sulphur-containing oil. The catalysts may contain conventional ingredients such as carriers.ALSO:Unsaturated fatty acids or their esters are isomerized by heating them to a temperature not exceeding 140 DEG C in presence of a catalyst prepared by reduction of a nickel or cobalt compound and comprising nickel or cobalt, nickel or cobalt silicate and a proportion of sulphur not exceeding 10 per cent based on the weight of the metal. Thus oleic acid, linseed oil fatty acids, linseed oil itself, other fatty oils of the drying, semi-drying and non-drying types, and alkyl esters of unsaturated fatty acids, particularly the ethyl esters, may be isomerized by this method. When unsaturated fatty acids or their esters with a single double bond, for example oleic acid or its esters, are treated by this method, the conversion of the cis-stereoisomer to the trans-stereoisomer causes a rise in melting point which is useful in the manufacture of margarine and other edible fats.
GB19719/50A 1949-08-31 1950-08-08 A process for isomerising unsaturated fatty acids or esters thereof Expired GB693981A (en)

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
NL148435A NL78104C (en) 1949-08-31 1949-08-31

Publications (1)

Publication Number Publication Date
GB693981A true GB693981A (en) 1953-07-08

Family

ID=63103723

Family Applications (1)

Application Number Title Priority Date Filing Date
GB19719/50A Expired GB693981A (en) 1949-08-31 1950-08-08 A process for isomerising unsaturated fatty acids or esters thereof

Country Status (8)

Country Link
US (1) US2692886A (en)
AT (1) AT178151B (en)
AU (1) AU149990B1 (en)
CH (1) CH305123A (en)
DE (1) DE883892C (en)
FR (1) FR1039559A (en)
GB (1) GB693981A (en)
NL (1) NL78104C (en)

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US2746979A (en) * 1951-06-14 1956-05-22 Lever Brothers Ltd Process for isomerizing unsaturated fatty acids or derivatives thereof

Families Citing this family (6)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
DE1089751B (en) * 1954-02-05 1960-09-29 Unilever Nv Process for isomerizing unsaturated fatty acids or their esters
DE954958C (en) * 1954-06-30 1956-12-27 Bayer Ag Process for rearrangement of ª ‰ -methylene glutaric dinitrile into ª ‰ -methylglutaconic dinitrile
US3274119A (en) * 1963-03-01 1966-09-20 Lever Brothers Ltd Transparent soap bar
US4203911A (en) * 1978-07-24 1980-05-20 Scm Corporation Process for conjugating unconjugated unsaturation of fatty acids or esters thereof
US4271066A (en) * 1979-11-05 1981-06-02 Arakawa Kagaku Kogyo Kabushiki Kaisha Process for disproportionating rosin, poly-unsaturated fatty acids and mixtures thereof
CN114480883B (en) * 2021-12-16 2023-11-21 成都先进金属材料产业技术研究院股份有限公司 Method for preparing high-purity vanadium pentoxide by removing silicon and chromium in vanadium solution through nickel ion cooperation

Family Cites Families (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US2553429A (en) * 1951-05-15 Semidrying oils
US2468799A (en) * 1943-10-20 1949-05-03 Lever Brothers Ltd Hydrogenating fat

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US2746979A (en) * 1951-06-14 1956-05-22 Lever Brothers Ltd Process for isomerizing unsaturated fatty acids or derivatives thereof

Also Published As

Publication number Publication date
NL78104C (en) 1955-06-15
CH305123A (en) 1955-02-15
DE883892C (en) 1953-07-23
AU149990B1 (en) 1950-10-19
AT178151B (en) 1954-04-10
US2692886A (en) 1954-10-26
FR1039559A (en) 1953-10-08

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