GB665264A - Improvements in or relating to improved detergent products and processes of preparing the same - Google Patents
Improvements in or relating to improved detergent products and processes of preparing the sameInfo
- Publication number
- GB665264A GB665264A GB23534/47A GB2353447A GB665264A GB 665264 A GB665264 A GB 665264A GB 23534/47 A GB23534/47 A GB 23534/47A GB 2353447 A GB2353447 A GB 2353447A GB 665264 A GB665264 A GB 665264A
- Authority
- GB
- United Kingdom
- Prior art keywords
- alkylolamines
- alkylolamine
- soap
- mixture
- reaction
- 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
- C11—ANIMAL OR VEGETABLE OILS, FATS, FATTY SUBSTANCES OR WAXES; FATTY ACIDS THEREFROM; DETERGENTS; CANDLES
- C11D—DETERGENT COMPOSITIONS; USE OF SINGLE SUBSTANCES AS DETERGENTS; SOAP OR SOAP-MAKING; RESIN SOAPS; RECOVERY OF GLYCEROL
- C11D10/00—Compositions of detergents, not provided for by one single preceding group
- C11D10/04—Compositions of detergents, not provided for by one single preceding group based on mixtures of surface-active non-soap compounds and soap
- C11D10/047—Compositions of detergents, not provided for by one single preceding group based on mixtures of surface-active non-soap compounds and soap based on cationic surface-active compounds and soap
-
- C—CHEMISTRY; METALLURGY
- C11—ANIMAL OR VEGETABLE OILS, FATS, FATTY SUBSTANCES OR WAXES; FATTY ACIDS THEREFROM; DETERGENTS; CANDLES
- C11D—DETERGENT COMPOSITIONS; USE OF SINGLE SUBSTANCES AS DETERGENTS; SOAP OR SOAP-MAKING; RESIN SOAPS; RECOVERY OF GLYCEROL
- C11D9/00—Compositions of detergents based essentially on soap
- C11D9/002—Non alkali-metal soaps
-
- C—CHEMISTRY; METALLURGY
- C11—ANIMAL OR VEGETABLE OILS, FATS, FATTY SUBSTANCES OR WAXES; FATTY ACIDS THEREFROM; DETERGENTS; CANDLES
- C11D—DETERGENT COMPOSITIONS; USE OF SINGLE SUBSTANCES AS DETERGENTS; SOAP OR SOAP-MAKING; RESIN SOAPS; RECOVERY OF GLYCEROL
- C11D1/00—Detergent compositions based essentially on surface-active compounds; Use of these compounds as a detergent
- C11D1/38—Cationic compounds
- C11D1/52—Carboxylic amides, alkylolamides or imides or their condensation products with alkylene oxides
- C11D1/523—Carboxylic alkylolamides, or dialkylolamides, or hydroxycarboxylic amides (R1-CO-NR2R3), where R1, R2 or R3 contain one hydroxy group per alkyl group
Landscapes
- 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)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
- Detergent Compositions (AREA)
Abstract
A process for the conversion of multiacylated alkylolamines formed by the reaction of alkylolamines with an acylating substance having 8-14 carbon atoms in the molecule, at a temperature sufficiently high to cause substantial reaction between the reactants, into monoacylated alkyl-olamines comprises incorporating into the reaction products of the alkylolamines and the acylating substance approximately 10-50 per cent of an alkylolamine soap of a higher fatty acid having more than 14 carbon atoms per molecule, based on the weight of the final mixture, and allowing the mixture to age at a lower temperature than the original reaction temperature. The acylating substances may be carboxylic acids, and the chlorides, esters or anhydrides of carboxylic acids. The alkanolamines may be primary and secondary alkylolamines such as monoethanolamine, monopropanolamine, diethanolamine, diglycerolamine, diisopropanolamine and dipropanolamine. The alkylolamine soap of the higher fatty acid may be added as such or may be formed by the addition of the higher fatty acid to the reaction mixture so that the soap is formed by the interaction of fatty acid and the free alkylolamine present in the mixture. Higher fatty acids which may be used include saturated or unsaturated fatty acids having about 16 to 18 carbon atoms in the molecule such as oleic, stearic, palmitic, or linoleic acid or mixtures of fatty acids obtained from soybean oil, corn oil or linseed oil. In an example, 1 mole. of coconut oil and 9 moles. of diethanolamine are heated together at 155 DEG C., with stirring, under an inert atmosphere of nitrogen until the titratable basicity of the mixture becomes constant. The reaction mixture is then cooled to about 70 DEG C. and 25 parts by weight of oleic acid added for every 100 parts of reaction mixture. The resulting mixture is then aged at about 60 DEG C. for about 36 hours. In another example 1 mole. of coconut oil fatty acids is heated with 3 moles of diethanolamine under a reduced pressure of about 40 mm. of mercury until the soap content is reduced to about 10 per cent, the reaction mixture cooled to about 90 DEG C. and about 20 per cent by weight of a mixture of stearic and palmitic acids added. The whole is allowed to age at 60 DEG C. for about 48 hours. The final products are said to be suitable detergents for washing fabrics (see Group III). U.S.A. Specification 2,483,253 is referred to.ALSO:Detergent compositions comprise a mixture of (1) the condensation products of alkylolamines and an acylating substance having 8-14 carbon atoms in the molecule, the products containing a substantial proportion of monoacylated alkylolamines, and (2) approximately 10-50 per cent of an alkylolamine soap of a higher fatty acid having more than 14 carbon atoms per molecule, based on the weight of the final detergent product. The acylating substance may be a carboxylic acid, a carboxylic acid chloride, a carboxylic acid ester or a carboxylic acid anhydride. Example of suitable alkylolamines are primary and secondary alkylolamines such as monoethanolamine, monopropanolamine, diethanolamine, diglycerolamine, diisopropanolamine, and dipropanolamine. Examples of suitable higher fatty acids are saturated or unsaturated single or mixed fatty acids preferably having about 16 to 18 carbon atoms in the molecule, such as oleic, stearic, palmitic or linoleic acid or the fatty acids of soya bean oil, corn oil and linseed oil. The acylated alkylolamines may be prepared by the two-stage process described in U.S.A. Specification 2,483,253 in which the multiacylated alkylolamines formed in the first stage of the process are converted into monoacylated alkylolamines in a second stage by an aging process in the presence of an alkylolamine soap of a fatty acid having 8-14 carbon atoms in the molecule, which soap functions as an aging catalyst. When the acylating substance having 8-14 carbon atoms in the molecule is a fatty acid, by controlling the reaction temperature and time, a complete conversion of the alkylolamine soap first formed into multiacylated alkylolamines may be prevented and sufficient soap left in the first stage reaction mixture to catalyze the conversion of the multiacylated into monoacylated alkylolamines in the second stage of the process. When employing an acylating substance incapable of forming soap with the alkylolamine, such as a triglyceride oil or fat, the reaction is carried out until the fat has substantially reacted with the alkylolamine, and then before the aging step a sufficient amount of 8-14 carbon atom fatty acid is added to form with any excess of alkylolamine the desired amount of soap. The compositions may also be prepared by reacting an excess of a primary or secondary alkylolamine with the acylating agent until condensation has proceeded to the desired stage, adding the higher fatty acid to the reaction mixture so as to form an alkylolamine soap, and allowing the resultant mixture to age (see Group IV(b)). In an example, 1 mole of coconut oil is reacted with 4.5 moles of dipropanolamine at 150 DEG C. at about 40 mm. of mercury pressure until the mixture has a constant titratable basicity. To the resulting mixture is added an additional 4.5 moles of dipropanolamine and then 7 per cent of coconut oil fatty acids. The whole is aged for about 48 hours at 60 DEG C. after which there is added 30 parts of oleic acid for every 100 parts of reaction product. Comparative data are given for washing tests carried out with tallow soap, with the acylated alkylolamine component containing excess alkylolamine and with the latter to which varying proportions of oleic acid have been added and the mixture aged.
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US733436A US2586496A (en) | 1947-03-08 | 1947-03-08 | Detergent composition and process of preparing same |
Publications (1)
Publication Number | Publication Date |
---|---|
GB665264A true GB665264A (en) | 1952-01-23 |
Family
ID=24947590
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
GB23534/47A Expired GB665264A (en) | 1947-03-08 | 1947-08-26 | Improvements in or relating to improved detergent products and processes of preparing the same |
Country Status (2)
Country | Link |
---|---|
US (1) | US2586496A (en) |
GB (1) | GB665264A (en) |
Families Citing this family (6)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
CA720078A (en) * | 1961-11-24 | 1965-10-19 | Swift And Company | Liquid detergent |
US3223186A (en) * | 1962-05-23 | 1965-12-14 | Pan American Corp | Method of drilling with air or gas |
FR2230401B1 (en) * | 1973-05-22 | 1976-10-08 | Fusey Pierre | |
US4040998A (en) * | 1975-07-17 | 1977-08-09 | Champion Spark Plug Company | Aqueous dispersion of ceramic slurry |
US4048122A (en) * | 1976-01-23 | 1977-09-13 | Barnes-Hind Pharmaceuticals, Inc. | Cleaning agents for contact lenses |
GB202205711D0 (en) * | 2022-04-19 | 2022-06-01 | Innospec Performance Chemicals Italia Srl | Compositions, methods and uses |
Family Cites Families (8)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
USRE21530E (en) * | 1940-08-13 | Acid substituted hydroxy alkylr- | ||
US1833899A (en) * | 1930-02-07 | 1931-12-01 | Larkin Company Inc | Soap |
GB414077A (en) * | 1932-12-21 | 1934-07-23 | Jack Leben | Improvements in and relating to soaps and the like |
US2089212A (en) * | 1936-06-08 | 1937-08-10 | Kritchevsky Wolf | Hydrotropic fatty material and method of making same |
US2404297A (en) * | 1943-06-04 | 1946-07-16 | Alrose Chemical Company | Deterging, wetting, and emulsifying compositions |
US2429445A (en) * | 1943-09-29 | 1947-10-21 | Ind Patent Corp | Process for reaction products of primary and secondary alkylolamines |
US2483253A (en) * | 1943-09-29 | 1949-09-27 | Swift & Co | Detergent composition |
US2404298A (en) * | 1945-08-10 | 1946-07-16 | Alrose Chemical Company | Saponaceous detergent having improved hard-water characteristics |
-
1947
- 1947-03-08 US US733436A patent/US2586496A/en not_active Expired - Lifetime
- 1947-08-26 GB GB23534/47A patent/GB665264A/en not_active Expired
Also Published As
Publication number | Publication date |
---|---|
US2586496A (en) | 1952-02-19 |
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