GB674870A - Improvements in process of reacting glyceride oils - Google Patents
Improvements in process of reacting glyceride oilsInfo
- 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
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.
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)
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 |
-
1949
- 1949-02-01 GB GB2766/49A patent/GB674870A/en not_active Expired
- 1949-02-02 NL NL656508436A patent/NL144674B/xx unknown
Cited By (2)
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 |
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