GB674870A - Improvements in process of reacting glyceride oils - Google Patents

Improvements in process of reacting glyceride oils

Info

Publication number
GB674870A
GB674870A GB2766/49A GB276649A GB674870A GB 674870 A GB674870 A GB 674870A GB 2766/49 A GB2766/49 A GB 2766/49A GB 276649 A GB276649 A GB 276649A GB 674870 A GB674870 A GB 674870A
Authority
GB
United Kingdom
Prior art keywords
acid
reacted
oil
glycerol
methyl alcohol
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
GB2766/49A
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.)
Baker Castor Oil Co
Original Assignee
Baker Castor Oil Co
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 Baker Castor Oil Co filed Critical Baker Castor Oil Co
Priority to GB2766/49A priority Critical patent/GB674870A/en
Priority to NL656508436A priority patent/NL144674B/xx
Publication of GB674870A publication Critical patent/GB674870A/en
Expired legal-status Critical Current

Links

Classifications

    • C—CHEMISTRY; METALLURGY
    • C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08G—MACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
    • C08G63/00—Macromolecular compounds obtained by reactions forming a carboxylic ester link in the main chain of the macromolecule
    • C08G63/02—Polyesters derived from hydroxycarboxylic acids or from polycarboxylic acids and polyhydroxy compounds
    • C08G63/12—Polyesters derived from hydroxycarboxylic acids or from polycarboxylic acids and polyhydroxy compounds derived from polycarboxylic acids and polyhydroxy compounds
    • C08G63/46—Polyesters chemically modified by esterification
    • C08G63/48—Polyesters chemically modified by esterification by unsaturated higher fatty oils or their acids; by resin acids
    • C—CHEMISTRY; METALLURGY
    • C11—ANIMAL OR VEGETABLE OILS, FATS, FATTY SUBSTANCES OR WAXES; FATTY ACIDS THEREFROM; DETERGENTS; CANDLES
    • C11C—FATTY ACIDS FROM FATS, OILS OR WAXES; CANDLES; FATS, OILS OR FATTY ACIDS BY CHEMICAL MODIFICATION OF FATS, OILS, OR FATTY ACIDS OBTAINED THEREFROM
    • C11C3/00—Fats, oils, or fatty acids by chemical modification of fats, oils, or fatty acids obtained therefrom
    • C11C3/04—Fats, oils, or fatty acids by chemical modification of fats, oils, or fatty acids obtained therefrom by esterification of fats or fatty oils
    • C—CHEMISTRY; METALLURGY
    • C11—ANIMAL OR VEGETABLE OILS, FATS, FATTY SUBSTANCES OR WAXES; FATTY ACIDS THEREFROM; DETERGENTS; CANDLES
    • C11C—FATTY ACIDS FROM FATS, OILS OR WAXES; CANDLES; FATS, OILS OR FATTY ACIDS BY CHEMICAL MODIFICATION OF FATS, OILS, OR FATTY ACIDS OBTAINED THEREFROM
    • C11C3/00—Fats, oils, or fatty acids by chemical modification of fats, oils, or fatty acids obtained therefrom
    • C11C3/04—Fats, oils, or fatty acids by chemical modification of fats, oils, or fatty acids obtained therefrom by esterification of fats or fatty oils
    • C11C3/06—Fats, oils, or fatty acids by chemical modification of fats, oils, or fatty acids obtained therefrom by esterification of fats or fatty oils with glycerol

Landscapes

  • Chemical & Material Sciences (AREA)
  • Oil, Petroleum & Natural Gas (AREA)
  • General Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Wood Science & Technology (AREA)
  • Engineering & Computer Science (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Health & Medical Sciences (AREA)
  • Medicinal Chemistry (AREA)
  • Polymers & Plastics (AREA)
  • Polyesters Or Polycarbonates (AREA)
  • Compositions Of Macromolecular Compounds (AREA)

Abstract

Partial esters of polyhydric alcohols, formed by methanolysis of a fatty oil, and reaction of the mixture of glycerol and methyl esters of fatty acid so obtained with added polyhydric alcohol (see Group IV (b)), are reacted with a polycarboxylic acid or anhydride, preferably at 200-300 DEG C., and in presence of an inert gas, to give a resin. In examples: (1) the partial ester as above prepared from dehydrated castor oil and added glycerol is heated with phthalic anhydride; (2) the partial ester from soyabean oil and pentaerythritol is heated with sebacic acid or maleic anhydride; (3) the partial ester from linseed oil and propylene glycol is heated with maleic acid. Other polycarboxylic compounds specified are fumaric acid, azelaic acid, malic acid, ketomalic acid, citric acid, phthalic acid, hemimellitic acid. Alcohols specified are glycocol, pentaerythritol mannitol, propylene glycol.ALSO:Partial esters of polyhydric alcohols and higher fatty acids are made by reacting a substantially neutral fatty oil with at least 6 mols. of methyl alcohol in presence of an esterification catalyst until the ester interchange reaction is substantially completed, and heating the thus-formed mixture of glycerine and fatty acid methyl esters with added polyhydric alcohol while distilling off the methyl alcohol. Fatty oils specified are soyabean, dehydrated castor, tung, oiticaca, linseed, or rapeseed. Catalysts specified include alkali and alkaline earth hydroxides and alcoholates, and certain quaternary ammonium hydroxides. Polyhydric alcohols specified are glycerol, pentaerythritol, mannitol, and propylene glycol. The esters are neutralized before use as, e.g. hydraulic fluids or plasticizers. They may be converted to resins by reaction with a polycarboxylic acid or anhydride (see Group IV (a)). In examples: (1) dehydrated castor oil is reacted with methyl alcohol in presence of caustic soda, and then with added glycerol; (2) soyabean oil is reacted with methyl alcohol in presence of phenyltrimethylammonium hydroxide, and the mixture of glycerol and methyl esters so obtained is reacted with pentaerythritol; (3) linseed oil is reacted with methyl alcohol in presence of sodium methylate, and the resulting mixture with sodium methylate; (4) tung oil is reacted with methyl alcohol in presence of lime, and the resulting mixture is reacted with glycerol.
GB2766/49A 1949-02-01 1949-02-01 Improvements in process of reacting glyceride oils Expired GB674870A (en)

Priority Applications (2)

Application Number Priority Date Filing Date Title
GB2766/49A GB674870A (en) 1949-02-01 1949-02-01 Improvements in process of reacting glyceride oils
NL656508436A NL144674B (en) 1949-02-01 1949-02-02

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
GB2766/49A GB674870A (en) 1949-02-01 1949-02-01 Improvements in process of reacting glyceride oils
NL656508436A NL144674B (en) 1949-02-01 1949-02-02

Publications (1)

Publication Number Publication Date
GB674870A true GB674870A (en) 1952-07-02

Family

ID=38528877

Family Applications (1)

Application Number Title Priority Date Filing Date
GB2766/49A Expired GB674870A (en) 1949-02-01 1949-02-01 Improvements in process of reacting glyceride oils

Country Status (2)

Country Link
GB (1) GB674870A (en)
NL (1) NL144674B (en)

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
WO2009085801A1 (en) * 2007-12-21 2009-07-09 Old Dominion University Research Foundation Direct conversion of biomass to biodiesel fuel

Cited By (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
WO2009085801A1 (en) * 2007-12-21 2009-07-09 Old Dominion University Research Foundation Direct conversion of biomass to biodiesel fuel
US8080679B2 (en) 2007-12-21 2011-12-20 Old Dominion University Research Foundation Direct conversion of biomass to biodiesel fuel

Also Published As

Publication number Publication date
NL144674B (en) 1955-07-15

Similar Documents

Publication Publication Date Title
US2383601A (en) Treating fats and fatty oils
US2494366A (en) Production of fatty esters
US4886893A (en) Process for the preparation of modified triglycerides
CN110041195A (en) A kind of fatty acid poleysters PVC plasticizer and preparation method thereof
ES249383A1 (en) Intermolecular alkyd-epoxy complexes
GB1007163A (en) Process for the production of hardenable products by polyesterification
GB674870A (en) Improvements in process of reacting glyceride oils
GB886750A (en) Preparation of carboxylic esters
GB634411A (en) Method of treating low-grade fatty stock to form alkyl esters therefrom
GB587532A (en) Improvements in or relating to alcoholysis of fatty glycerides
US2360393A (en) Alcoholysis catalysts
GB629490A (en) Improvements in or relating to the manufacture of oil-modified alkyd resins
GB952181A (en) Acetals
US2345041A (en) Esters of sulphotricarballylic acids
US2997484A (en) Method of epoxidation of unsaturated
GB664052A (en) Improvements in or relating to synthetic lubricants
GB709011A (en) Improvements in or relating to the production of polymeric products from styrene andunsaturated fatty compounds
US2947766A (en) Acyloxy-halo derivatives of aliphatic acids and their esters
US2411111A (en) Treatment of polyene compounds
US2655487A (en) Tetrahydrophthalic acid half ester compounds
GB953357A (en) A process for the preparation of urethane modified vegetable oils
GB744273A (en) Improvements in or relating to the production of modified alkyd resins
GB779052A (en) Esters and a process for their production
GB767780A (en) Improvements in trans n-carbamylamic esters
GB707002A (en) Process for the preparation of improved oil-modified alkyd resins