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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 same

Info

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
Application number
GB23534/47A
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.)
JBS USA LLC
Original Assignee
Swift and Co Inc
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 Swift and Co Inc filed Critical Swift and Co Inc
Publication of GB665264A publication Critical patent/GB665264A/en
Expired legal-status Critical Current

Links

Classifications

    • CCHEMISTRY; METALLURGY
    • C11ANIMAL OR VEGETABLE OILS, FATS, FATTY SUBSTANCES OR WAXES; FATTY ACIDS THEREFROM; DETERGENTS; CANDLES
    • C11DDETERGENT COMPOSITIONS; USE OF SINGLE SUBSTANCES AS DETERGENTS; SOAP OR SOAP-MAKING; RESIN SOAPS; RECOVERY OF GLYCEROL
    • C11D10/00Compositions of detergents, not provided for by one single preceding group
    • C11D10/04Compositions of detergents, not provided for by one single preceding group based on mixtures of surface-active non-soap compounds and soap
    • C11D10/047Compositions 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
    • CCHEMISTRY; METALLURGY
    • C11ANIMAL OR VEGETABLE OILS, FATS, FATTY SUBSTANCES OR WAXES; FATTY ACIDS THEREFROM; DETERGENTS; CANDLES
    • C11DDETERGENT COMPOSITIONS; USE OF SINGLE SUBSTANCES AS DETERGENTS; SOAP OR SOAP-MAKING; RESIN SOAPS; RECOVERY OF GLYCEROL
    • C11D9/00Compositions of detergents based essentially on soap
    • C11D9/002Non alkali-metal soaps
    • CCHEMISTRY; METALLURGY
    • C11ANIMAL OR VEGETABLE OILS, FATS, FATTY SUBSTANCES OR WAXES; FATTY ACIDS THEREFROM; DETERGENTS; CANDLES
    • C11DDETERGENT COMPOSITIONS; USE OF SINGLE SUBSTANCES AS DETERGENTS; SOAP OR SOAP-MAKING; RESIN SOAPS; RECOVERY OF GLYCEROL
    • C11D1/00Detergent compositions based essentially on surface-active compounds; Use of these compounds as a detergent
    • C11D1/38Cationic compounds
    • C11D1/52Carboxylic amides, alkylolamides or imides or their condensation products with alkylene oxides
    • C11D1/523Carboxylic 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.
GB23534/47A 1947-03-08 1947-08-26 Improvements in or relating to improved detergent products and processes of preparing the same Expired GB665264A (en)

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)

* Cited by examiner, † Cited by third party
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)

* Cited by examiner, † Cited by third party
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

Also Published As

Publication number Publication date
US2586496A (en) 1952-02-19

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