US2634239A - Detergent composition - Google Patents

Detergent composition Download PDF

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US2634239A
US2634239A US101247A US10124749A US2634239A US 2634239 A US2634239 A US 2634239A US 101247 A US101247 A US 101247A US 10124749 A US10124749 A US 10124749A US 2634239 A US2634239 A US 2634239A
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piperazine
soap
carbon atoms
water
soaps
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US101247A
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Malkemus John David
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Colgate Palmolive Co
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Colgate Palmolive Co
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    • 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
    • C11D9/04Compositions of detergents based essentially on soap containing compounding ingredients other than soaps
    • C11D9/22Organic compounds, e.g. vitamins
    • C11D9/30Organic compounds, e.g. vitamins containing nitrogen
    • 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
    • C11D1/00Detergent compositions based essentially on surface-active compounds; Use of these compounds as a detergent
    • C11D1/38Cationic compounds
    • C11D1/58Heterocyclic compounds

Definitions

  • the present invention relates to novel deter-1 gent compositions and to a process for producing said compositiona
  • soap in washing operations is very old, and in soft water (that is, water containing at most only a very small amount of mineral salts) soap is a very efficient and satisfactory cleansing agent.
  • soft water that is, water containing at most only a very small amount of mineral salts
  • soap is a very efficient and satisfactory cleansing agent.
  • natural water usually contains salts, such as calcium and magnesium salts, which decompose water soluble soaps to form water-insoluble soaps.
  • the formation of such water-insoluble soaps decreases the apparent efficiency of the soap used by requiring that a greater. amount of soap be added to the solution to remove the salts and still have enough water-soluble soap present for an efiective washing concentration.
  • the water-insoluble soaps formed have another disadvantage in that they appear in the wash water as curds or scum which-settle upon the material being washed.
  • a further difficulty is that they are often formed within the interstices of cloth during laundering and are extremely hard to remove.
  • the insoluble soaps may still be formed therein during rinsing, as the soluble salts in the rinse water react with the soluble soap in the interstices to form these insoluble soaps.
  • the presence of such curds or scum gives the cloth a grayish or yellowish cast in many cases, which is most undesirable, and frequently imparts an unpleasant rancid odor.
  • Another object of the present invention is the provision or a detergent composition which is very soluble in water and which has high detersive efficiency in hard Water as well as soft.
  • This invention further provides a novel methodfor producing new compositions of high deter-.
  • the soaps comprised by the novel compositions of the invention are the so-called water-soluble soaps of the soap-making art and include sodium, potassium, ammonium and amine salts of the higher fatty acids, that is, those having about eight to about twenty carbon atoms per molecule.
  • Such soaps may be represented by the following general formula:
  • R is an alkyl radical containing from about eight to about twenty carbon atoms
  • M is a monovalent radical e. g. alkali metal, ammonium or substituted ammonia group.
  • These soaps are normally prepared from such naturally-occurring esters as coconut oil, palm oil, olive oil, cottonseed oil, tung oil, corn oil, castor oil, soya bean oil, W001 fat, tallow, whale oil, menhaden e11, pilchard oil, sardine oil, herring oil, and the like, as well as mixtures of these.
  • aliphatic carboxylic acid monoeste'r or monoether derivatives of N,'N'-dialkanol piperazines which may be mixed with soaps to form the new detersive compositions of the invention and to achieve the desirable results described, are those represented by the general structural formula:
  • R is an alkyl or acyl radical having about five to about twenty-three, preferably about eight to about eighteen, carbon atoms;
  • a and B are ethylene radicals wherein any number of hydrogens (none, one or more) may be replaced by alkyl radicals, preferably of not more than two carbon atoms; and m and n are small integers, say two to about five, preferably two.
  • the carbon chain represented by B may be straight or branched, saturated or unsaturated, and may be either unsubstituted or substituted by substituents such as halogens, hydroxyls, acyl groups, acyloxy groups, alkoxy groups, aryl groups, etc., although it is generally preferred that substituent groups of hydrophilic character be located near or adjacent to the piperazyl alkoxy group.
  • substituents such as halogens, hydroxyls, acyl groups, acyloxy groups, alkoxy groups, aryl groups, etc.
  • the acyl group may be the residue of any suitable carboxylic acid, including lauric acid, myristic acid, palmitic acid, stearic acid, hydroxystearic acid, oleic acid, linoleic acid, linolenic acid, ricinoleic acid, caproic acid, isocaprylic acid, a-aminocapric acid, undecylenic acid, lignoceric acid, erucic acid, lauryl succinic acid, chloropalmitic acid, mixed coconut oil fatty acids, mixed tallow fatty acids, mixtures of any of these acids, etc.
  • carboxylic acid including lauric acid, myristic acid, palmitic acid, stearic acid, hydroxystearic acid, oleic acid, linoleic acid, linolenic acid, ricinoleic acid, caproic acid, isocaprylic acid, a-aminocapric acid, undecylenic acid, lig
  • the alkyl group may be any corresponding to a suitable carboxylic acid, such as the above-mentioned, including lauryl, myristyl, palmityl, stearyl, hydroxystearyl, oleyl, linoleyl, linolenyl, ricinoleyl, hexyl, isoctyl, B-aminodecyl, etc.
  • the dialkanol piperazine residue of the ester or ether employed may be symmetrical or mixed. That is, m and it may be the same number or they may be different numbers.
  • symmetrical dialkanol piperazines such as diethanol piperazine, dipropanol piperazine, diisopropanol piperazine, etc.
  • mixed piperazines of the type of 13- propanol-d-fi-ethanol piperazine, l-fi-ethanollv-butanol piperazine, etc. can also be used.
  • Suitable esters for use in the compositions of this invention include diethanol piperazine monolaurate, ricinoleic acid monoester of diethanol piperazine, di-w-butanol piperazine monostearate, coconut oil fatty acid monoesters of diethanol piperazine, etc.
  • Ethers suitable for employment in the novel compositions include 1-(2- lauroxyethyl) -4-(2- hydroxyethyl) piperazine, 3,6 dimethyl 1 (2 myristoxypropyl) 4- (Z-hydroxypropyl) -piperazine.
  • dialkanol piperazine monoester or monoether vary greatly, depending largely upon the use intended for the composition. Again, given any specific characteristics desired for a particular use, the optimum proportions employed will also vary with the particular active ingredients (both soap and piperazine derivative) or mixtures of ingredients used; with the proportion of other ingredients present, if any; and to some degree with the strength or concentration of solution to be formed in use.
  • compositions of high detergency can be formed by mixing small proportions of soap with large proportions of a dialkanol piperazine monoester or monoether (as will be pointed out more fully hereinafter), so that the compositions of the invention comprises mixtures of these ingredients in all proportions
  • the greatest value and usefulness of the present invention lie in compositions having less than of the dialkanol piperazine derivative based on the total weight of the composition.
  • the dialkanol piperazine monoester or monoether may be incorporated with the soap to form the novel composition of the invention at any point during the soap manufacturing process at which subsequent operations will not destroy or objectionably modify the piperazine derivative or cause a deleterious reaction between the piperazine derivative and any other material in the composition.
  • novel compositions may be made up in solutions, preferably concentrated, or a dry or partially hydrated solid product or a paste may be formed.
  • the product may be made in a more or less finely divided condition, which permits its ready transformation into flakes or other physical forms, for example by passing between a pair of properly spaced rolls, or by milling or pressing into cakes, or by other means, with or without addition of modifying agents.
  • dialkanol piperazine ester and soap or ether derivative may be added separately to washing solutions.
  • Adjuvant materials may be admixed with the novel compositions by mixing such materials with the fatty compounds (whether glycerides, alkyl esters or fatty acids) and/or the neutralizing or saponifying agents before neutralization or flashing, by simultaneously flashing a second solution containing such adjuvant materials, and/or by mixing the final product herewith.
  • the adjuvant materials may be added before, after or simultaneously with the piperazine derivative.
  • Such adjuvant materials may include any of the substances employed by the art in admixture with soaps generally, such as the common inorganic builders of the type of carbonates, phosphates, silicates, etc., and including certain of the sulphated and/or sulphonated organic surface-active agents known to the detergent art.
  • soaps generally, such as the common inorganic builders of the type of carbonates, phosphates, silicates, etc., and including certain of the sulphated and/or sulphonated organic surface-active agents known to the detergent art.
  • care is exercised to avoid the use of any material which would remove or otherwise substantially diminish the effectiveness of the dialkanol piperazine monoester or monoether incorporated.
  • the type of addition agent will depend upon the ultimate use of the new compos1 ion.
  • novel and improved detersive, dispersing and emulsifying agents of this invention comprising fatty acid soaps (with or Without adjuvant materials) and a proportion of the dialkanol-piperazine monoester and/or monoether described, produce solutions which are efficient sisting of alkali metal, ammonium and substituted ammonia groups, and an amount of a piperazine derivative equivalent to about to about 75% by weight of the total composition, said piperazine derivative being represented by the structural formula:
  • R is a member of the group consisting of alkyl and acyl radicals having about 8 to about 18 carbon atoms, and m and n are integers of 2 to about 5.
  • a detergent composition comprising essentially a water-soluble soap represented by the structural formula:
  • RCOOM where R is a member of the group consisting of alkyl and acyl radicals having about 5 to about 23 carbon atoms.
  • a detergent composition comprising essentially a water-soluble salt of higher fatty acids containing from about 8 to about 20 carbon atoms per molecule with an alkali metal, and an amount of a fatty acid monoester of 1,4-di(B-hydroxy ethyl) piperazine equivalent to about 5% to about 75% by weight of said detergent composition and wherein the fatty acid residue of said piperazine contains about 5 to about 23 carbon atoms.
  • a detergent composition comprising essentially a water-soluble salt of higher fatty acids containing from about 8 to about 20 carbon atoms per molecule with ammonium and an amount of a fatty acid monoester' of lA-diQB-hydroxy ethyl) piperazine equivalent to about 5% to about 75% by weight of said detergent composition and wherein the fatty acid residue of said piperazine contains about 5 to about 23 carbon atoms.
  • a detergent composition comprising essentially a water-soluble salt of higher fatty acids containing from about 8 to about 20 carbon atoms per molecule with an alkali metal, and an amount of a fatty acid monoether of 1,4-di(fi-hydroxy ethyl) piperazine equivalent to about 5% to about 75% by weight of said detergent composition and wherein the fatty acid residue of said piperazine contains about 5 to about 23 carbon atoms.
  • a detergent composition comprising essentially a water-soluble salt of higher fatty acids containing from about 8 to about 20 carbon atoms per molecule with ammonium, and an amount of a fatty acid monoether of 1,4-di(,8-hydroxy ethyl) piperazine equivalent to about 5% to about 75% by weight of said detergent composition and wherein the fatty acid residue of said piperazine contains about 5 to about 23 carbon atoms.
  • a detergent composition comprising essentially a water-soluble soap of the formula:
  • RCOOM where R is an alkyl radical containing from about 8 to about carbon atoms, M is selected from the class consisting of alkali metal, ammonium and substituted ammonia groups, and an amount of l-(p-lauroxy ethyl) -4(p-hydroxy ethyl) piperazine equivalent to about 10% to about by weight based upon the total weight of the soap and the piperazine material.
  • a process for preparing surface active compositions of high detersive efficiency which comprises incorporating in a water soluble soap which consists essentially of the salt of fatty acids containing at least about 8 carbon atoms per molecule and a material selected from the class consisting of alkali metal, ammonium, and substituted ammonia groups, an amount of a piperazine derivative equivalent to about 5% to about 75% by weight based upon the total weight of the soap and the piperazine derivative, said piperazine derivative being represented by the structural formula:
  • ber of hydrogens in the ethylene radical are re-' placed by' alkyl radicals of not more than 2 carbon atoms, and m and n are integers of 2 to about 5.
  • a process of preparing surface active compositions in solid form which compositions have improved detersive efficiency in aqueous solutions comprising wet mixing a water soluble soap which consists essentially of the salt of fatty acids containing at least about 8 carbon atoms per molecule and a material selected from the group consisting of alkali metal, ammonium and ammonia groups, with an amount of an aliphatic carboxylic fatty acid ester derivative of N,N'-diethanolamine piperazine equivalent to about 5% to about 75% by weight based upon the total weight of the soap and the piperazine derivative, said piperazine being represented by the structural formula:
  • R is a member of the group consisting of acyl and substituted acyl radicals having about 8 to 20 carbon atoms per molecule
  • a and B are members of the group consisting of an ethylene radical and alkyl derivatives thereof wherein any number of hydrogens in the ethylene radical are replaced by alkyl radicals of not more than 2 carbon atoms, and m and n are integers of 2 to about 5, and subjecting said soap and piperazine derivative mixture to a drying operation to produce the surface active composition insolid form.
  • a detergent composition comprising a mixture of water soluble soaps which form water insoluble scums in hard water, said soaps consisting essentially of the salts of fatty acids containing from about 8 to about 20 carbon atoms per molecule and a material selected from the class consisting of alkali metal, ammonium and sub- 7 stituted ammonia groups, and an aliphatic carwhere R is a member of the group consisting of alkyl and substituted alkyl radicals having about to 23 carbon atoms, A and B are members of the group consisting of an ethylene radical and alkyl derivatives thereof wherein any number of hydrogens in the ethylene radical are replaced by alkyl radicals of not more than 2 carbon atoms, and m and n are integers of 2 to about 5.
  • a detergent composition comprising a mixture of water soluble soaps which form water insoluble lime soaps in hard water, said water soluble soaps consisting essentially of the salts of fatty acids containing at least about 8 carbon atoms per molecule and a material selected from the class consisting of alkali metal, ammonium and substituted ammonia groups, and a lime soap dispersing agent consisting of an aliphatic car- 10 boxylic acid ester derivative of N,N'-diethano1 piperazine in an amount equivalent to about 5% to about by weight based upon the total weight of the soaps and the piperazine derivative, said piperazine derivative being represented by --the structural formula:
  • a RO-(OHzM-N/ N- cHl)fl-on where R is a member of the class consisting of acyl and substituted acyl radicals having about 5 ,to about 23 carbon atoms,
  • a and B are members :of the group consisting of an ethylene radical and alkyl derivatives thereof wherein any number of hydrogens in the ethylene radical are replaced by alkyl radicals of not more than 2 carbon atoms, and m and n are integers of 2 to about 5.

Description

Patented Apr. 7, 1953 DETERGENT COMPOSITION John David Malkemus, Allendale, N. 3., assignor to Golgate-Palmolive-Peet Company, Jersey City, N. J a corporation of Delaware No Draining. Application June 24, 1949, Serial No. 101,247
is Glaims. (01. 252- 117) The present invention relates to novel deter-1 gent compositions and to a process for producing said compositiona The use of soap in washing operations is very old, and in soft water (that is, water containing at most only a very small amount of mineral salts) soap is a very efficient and satisfactory cleansing agent. However, natural water usually contains salts, such as calcium and magnesium salts, which decompose water soluble soaps to form water-insoluble soaps. The formation of such water-insoluble soaps decreases the apparent efficiency of the soap used by requiring that a greater. amount of soap be added to the solution to remove the salts and still have enough water-soluble soap present for an efiective washing concentration. v
The water-insoluble soaps formed, usually comprising calcium and magnesium soaps, have another disadvantage in that they appear in the wash water as curds or scum which-settle upon the material being washed. A further difficulty is that they are often formed within the interstices of cloth during laundering and are extremely hard to remove. Moreover, even if all the soap is added to the water before introduction of the cloth, so that only the solution of solublesoap gets into the interstices during the washing operation, the insoluble soaps may still be formed therein during rinsing, as the soluble salts in the rinse water react with the soluble soap in the interstices to form these insoluble soaps. The presence of such curds or scum gives the cloth a grayish or yellowish cast in many cases, which is most undesirable, and frequently imparts an unpleasant rancid odor.
From time to time, various substances have been proposed for admixture with soaps in order to modify their properties and to render them more efiicient for use in hard waters. Some of these substances have had limited success, in that curds and scums have largely been eliminated. However, in a large number of such instances the detersive efficiency has been considerably impaired. a I
It is an object or the present invention to provide a new composition of matter of high detersive efficiency aqueous solution but with none of the undesirable scum-forming character istics of soaps.
It is another object of this invention to pro-. vide a highly detergent composition capable of dispersing hard water scum. It is also an object of the inventionto provide a soap-containing composition which effectively disperses curds in hard water without substantial impairment of the detersive efiiciency of the soap.
Another object of the present invention is the provision or a detergent composition which is very soluble in water and which has high detersive efficiency in hard Water as well as soft.
This invention further provides a novel methodfor producing new compositions of high deter-.
gency.
Other objects and advantages of the invention willbe apparent from the following description.
According to the present invention, it has now been found that the incorporation of a cationic surface-active agent of the type of aliphatic carboxylic acid monoester or monoetherderivatives of a dialkanol piperazine with a fatty acid soap provides a composition or high detergency (even as compared with soaps alone) and of excellent lime soap dispersing characteristics.
The soaps comprised by the novel compositions of the invention are the so-called water-soluble soaps of the soap-making art and include sodium, potassium, ammonium and amine salts of the higher fatty acids, that is, those having about eight to about twenty carbon atoms per molecule. Such soaps may be represented by the following general formula:
where R is an alkyl radical containing from about eight to about twenty carbon atoms; and M is a monovalent radical e. g. alkali metal, ammonium or substituted ammonia group. These soaps are normally prepared from such naturally-occurring esters as coconut oil, palm oil, olive oil, cottonseed oil, tung oil, corn oil, castor oil, soya bean oil, W001 fat, tallow, whale oil, menhaden e11, pilchard oil, sardine oil, herring oil, and the like, as well as mixtures of these.
The aliphatic carboxylic acid monoeste'r or monoether derivatives of N,'N'-dialkanol piperazines, which may be mixed with soaps to form the new detersive compositions of the invention and to achieve the desirable results described, are those represented by the general structural formula:
where R, is an alkyl or acyl radical having about five to about twenty-three, preferably about eight to about eighteen, carbon atoms; A and B are ethylene radicals wherein any number of hydrogens (none, one or more) may be replaced by alkyl radicals, preferably of not more than two carbon atoms; and m and n are small integers, say two to about five, preferably two. The carbon chain represented by B may be straight or branched, saturated or unsaturated, and may be either unsubstituted or substituted by substituents such as halogens, hydroxyls, acyl groups, acyloxy groups, alkoxy groups, aryl groups, etc., although it is generally preferred that substituent groups of hydrophilic character be located near or adjacent to the piperazyl alkoxy group. Where R is an alkyl or substituted alkyl group, the material mixed with the soap in accordance with the invention is an ether; and Where R is an acyl or substituted acyl group, the compound thus employed is an ester.
In the case of the compounds being an ester, the acyl group may be the residue of any suitable carboxylic acid, including lauric acid, myristic acid, palmitic acid, stearic acid, hydroxystearic acid, oleic acid, linoleic acid, linolenic acid, ricinoleic acid, caproic acid, isocaprylic acid, a-aminocapric acid, undecylenic acid, lignoceric acid, erucic acid, lauryl succinic acid, chloropalmitic acid, mixed coconut oil fatty acids, mixed tallow fatty acids, mixtures of any of these acids, etc. Where the compound is an ether, the alkyl group may be any corresponding to a suitable carboxylic acid, such as the above-mentioned, including lauryl, myristyl, palmityl, stearyl, hydroxystearyl, oleyl, linoleyl, linolenyl, ricinoleyl, hexyl, isoctyl, B-aminodecyl, etc.
The dialkanol piperazine residue of the ester or ether employed may be symmetrical or mixed. That is, m and it may be the same number or they may be different numbers. In general, it is preferred to employ symmetrical dialkanol piperazines such as diethanol piperazine, dipropanol piperazine, diisopropanol piperazine, etc., and especially the symmetrical dialkanol piperazines having both hydroxyl groups in omega position with respect to the piperazyl radical. However, mixed piperazines of the type of 13- propanol-d-fi-ethanol piperazine, l-fi-ethanollv-butanol piperazine, etc. can also be used.
Suitable esters for use in the compositions of this invention include diethanol piperazine monolaurate, ricinoleic acid monoester of diethanol piperazine, di-w-butanol piperazine monostearate, coconut oil fatty acid monoesters of diethanol piperazine, etc. Ethers suitable for employment in the novel compositions include 1-(2- lauroxyethyl) -4-(2- hydroxyethyl) piperazine, 3,6 dimethyl 1 (2 myristoxypropyl) 4- (Z-hydroxypropyl) -piperazine.
The relative proportions of the dialkanol piperazine monoester or monoether and the soap in the new compositions vary greatly, depending largely upon the use intended for the composition. Again, given any specific characteristics desired for a particular use, the optimum proportions employed will also vary with the particular active ingredients (both soap and piperazine derivative) or mixtures of ingredients used; with the proportion of other ingredients present, if any; and to some degree with the strength or concentration of solution to be formed in use. While useful solubilizing, wetting and emulsifying compositions of high detergency can be formed by mixing small proportions of soap with large proportions of a dialkanol piperazine monoester or monoether (as will be pointed out more fully hereinafter), so that the compositions of the invention comprises mixtures of these ingredients in all proportions, it is contemplated that the greatest value and usefulness of the present invention lie in compositions having less than of the dialkanol piperazine derivative based on the total weight of the composition. In general, it is preferred to incorporate about 5% to about 75%, and more preferably about 10% to about 50% by weight of the monoester based upon the total weight of the soap and the dialkanol piperazin derivative.
The dialkanol piperazine monoester or monoether may be incorporated with the soap to form the novel composition of the invention at any point during the soap manufacturing process at which subsequent operations will not destroy or objectionably modify the piperazine derivative or cause a deleterious reaction between the piperazine derivative and any other material in the composition. In general, it is preferred to add the piperazine derivative at a point in the manufacturing subsequent to the saponifying or neutralizing step. This may be accomplished by adding the piperazine derivative in solid form or in solution to molten soap in the soap kettles, by mixing or milling the piperazine derivative with solid soap in comminuted form, or by adding the piperazine derivative to a soap solution and thereafter subjecting the solution containing soap and piperazine derivative to spraydrying, roll-drying, etc., to form a solid composition.
The novel compositions, if desired, may be made up in solutions, preferably concentrated, or a dry or partially hydrated solid product or a paste may be formed. The product may be made in a more or less finely divided condition, which permits its ready transformation into flakes or other physical forms, for example by passing between a pair of properly spaced rolls, or by milling or pressing into cakes, or by other means, with or without addition of modifying agents. Also the dialkanol piperazine ester and soap or ether derivative may be added separately to washing solutions.
Adjuvant materials may be admixed with the novel compositions by mixing such materials with the fatty compounds (whether glycerides, alkyl esters or fatty acids) and/or the neutralizing or saponifying agents before neutralization or flashing, by simultaneously flashing a second solution containing such adjuvant materials, and/or by mixing the final product herewith. When added after neutralization or saponification, the adjuvant materials may be added before, after or simultaneously with the piperazine derivative. Such adjuvant materials may include any of the substances employed by the art in admixture with soaps generally, such as the common inorganic builders of the type of carbonates, phosphates, silicates, etc., and including certain of the sulphated and/or sulphonated organic surface-active agents known to the detergent art. In employing such adjuvant materials, care is exercised to avoid the use of any material which would remove or otherwise substantially diminish the effectiveness of the dialkanol piperazine monoester or monoether incorporated. The type of addition agent will depend upon the ultimate use of the new compos1 ion.
The novel and improved detersive, dispersing and emulsifying agents of this invention, comprising fatty acid soaps (with or Without adjuvant materials) and a proportion of the dialkanol-piperazine monoester and/or monoether described, produce solutions which are efficient sisting of alkali metal, ammonium and substituted ammonia groups, and an amount of a piperazine derivative equivalent to about to about 75% by weight of the total composition, said piperazine derivative being represented by the structural formula:
where R is a member of the group consisting of alkyl and acyl radicals having about 8 to about 18 carbon atoms, and m and n are integers of 2 to about 5.
4. A detergent composition comprising essentially a water-soluble soap represented by the structural formula:
RCOOM where R is a member of the group consisting of alkyl and acyl radicals having about 5 to about 23 carbon atoms.
5. A detergent composition comprising essentially a water-soluble salt of higher fatty acids containing from about 8 to about 20 carbon atoms per molecule with an alkali metal, and an amount of a fatty acid monoester of 1,4-di(B-hydroxy ethyl) piperazine equivalent to about 5% to about 75% by weight of said detergent composition and wherein the fatty acid residue of said piperazine contains about 5 to about 23 carbon atoms. f
6. A detergent composition comprising essentially a water-soluble salt of higher fatty acids containing from about 8 to about 20 carbon atoms per molecule with ammonium and an amount of a fatty acid monoester' of lA-diQB-hydroxy ethyl) piperazine equivalent to about 5% to about 75% by weight of said detergent composition and wherein the fatty acid residue of said piperazine contains about 5 to about 23 carbon atoms.
7. A detergent composition comprising essentially a water-soluble salt of higher fatty acids containing from about 8 to about 20 carbon atoms per molecule with an alkali metal, and an amount of a fatty acid monoether of 1,4-di(fi-hydroxy ethyl) piperazine equivalent to about 5% to about 75% by weight of said detergent composition and wherein the fatty acid residue of said piperazine contains about 5 to about 23 carbon atoms.
8. A detergent composition comprising essentially a water-soluble salt of higher fatty acids containing from about 8 to about 20 carbon atoms per molecule with ammonium, and an amount of a fatty acid monoether of 1,4-di(,8-hydroxy ethyl) piperazine equivalent to about 5% to about 75% by weight of said detergent composition and wherein the fatty acid residue of said piperazine contains about 5 to about 23 carbon atoms.-
9. A detergent composition comprising essentially a water-soluble soap of the formula:
RCOOM where R is an alkyl radical containing from about 8 to about carbon atoms, M is selected from the class consisting of alkali metal, ammonium and substituted ammonia groups, and an amount of l-(p-lauroxy ethyl) -4(p-hydroxy ethyl) piperazine equivalent to about 10% to about by weight based upon the total weight of the soap and the piperazine material.
10. A process for preparing surface active compositions of high detersive efficiency which comprises incorporating in a water soluble soap which consists essentially of the salt of fatty acids containing at least about 8 carbon atoms per molecule and a material selected from the class consisting of alkali metal, ammonium, and substituted ammonia groups, an amount of a piperazine derivative equivalent to about 5% to about 75% by weight based upon the total weight of the soap and the piperazine derivative, said piperazine derivative being represented by the structural formula:
ber of hydrogens in the ethylene radical are re-' placed by' alkyl radicals of not more than 2 carbon atoms, and m and n are integers of 2 to about 5.
11. A process of preparing surface active compositions in solid form which compositions have improved detersive efficiency in aqueous solutions comprising wet mixing a water soluble soap which consists essentially of the salt of fatty acids containing at least about 8 carbon atoms per molecule and a material selected from the group consisting of alkali metal, ammonium and ammonia groups, with an amount of an aliphatic carboxylic fatty acid ester derivative of N,N'-diethanolamine piperazine equivalent to about 5% to about 75% by weight based upon the total weight of the soap and the piperazine derivative, said piperazine being represented by the structural formula:
where R is a member of the group consisting of acyl and substituted acyl radicals having about 8 to 20 carbon atoms per molecule, A and B are members of the group consisting of an ethylene radical and alkyl derivatives thereof wherein any number of hydrogens in the ethylene radical are replaced by alkyl radicals of not more than 2 carbon atoms, and m and n are integers of 2 to about 5, and subjecting said soap and piperazine derivative mixture to a drying operation to produce the surface active composition insolid form.
12. A detergent composition comprising a mixture of water soluble soaps which form water insoluble scums in hard water, said soaps consisting essentially of the salts of fatty acids containing from about 8 to about 20 carbon atoms per molecule and a material selected from the class consisting of alkali metal, ammonium and sub- 7 stituted ammonia groups, and an aliphatic carwhere R is a member of the group consisting of alkyl and substituted alkyl radicals having about to 23 carbon atoms, A and B are members of the group consisting of an ethylene radical and alkyl derivatives thereof wherein any number of hydrogens in the ethylene radical are replaced by alkyl radicals of not more than 2 carbon atoms, and m and n are integers of 2 to about 5.
13. A detergent composition comprising a mixture of water soluble soaps which form water insoluble lime soaps in hard water, said water soluble soaps consisting essentially of the salts of fatty acids containing at least about 8 carbon atoms per molecule and a material selected from the class consisting of alkali metal, ammonium and substituted ammonia groups, and a lime soap dispersing agent consisting of an aliphatic car- 10 boxylic acid ester derivative of N,N'-diethano1 piperazine in an amount equivalent to about 5% to about by weight based upon the total weight of the soaps and the piperazine derivative, said piperazine derivative being represented by --the structural formula:
A RO-(OHzM-N/ N- cHl)fl-on where R is a member of the class consisting of acyl and substituted acyl radicals having about 5 ,to about 23 carbon atoms, A and B are members :of the group consisting of an ethylene radical and alkyl derivatives thereof wherein any number of hydrogens in the ethylene radical are replaced by alkyl radicals of not more than 2 carbon atoms, and m and n are integers of 2 to about 5.
J. DAVID MALKEMUS.
REFERENCES CITED The following references are of record in the file of this patent:
UNITED STATES PATENTS Number Name Date 1,822,108 Murrill Sept. 8, 1931 2,421,707 Malkemus June 3, 1947

Claims (1)

1. A DETERGENT COMPOSITION COMPRISING ESSENTIALLY A WATER-SOLUBLE SOAP REPRESENTED BY THE STRUCTURAL FORMULA: RCOOM, WHERE R IS AN ALKYL RADICAL CONTAINING FROM ABOUT 8 TO ABOUT 20 CARBON ATOMS AND M IS A MONOVALENT RADICAL SELECTED FROM THE CLASS CONSISTING OF ALKALI METAL, AMMONIUM AND SUBSTITUTED AMMONIUM GROUPS, AND AN AMOUNT OF A PIPERAZINE DERIVATIVE EQUIVALENT TO ABOUT 5% TO ABOUT 75% BY WEIGHT OF THE TOTAL COMPOSITION, SAID PIPERAZINE DERIVATIVE BEING REPRESENTED BY THE STRUCTURAL FORMULA:
US101247A 1949-06-24 1949-06-24 Detergent composition Expired - Lifetime US2634239A (en)

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Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US3325414A (en) * 1963-10-01 1967-06-13 Colgate Palmolive Co Heavy duty detergent composition containing a quaternary ammonium salt

Citations (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US1822108A (en) * 1928-08-07 1931-09-08 Vanderbilt Co R T Stabilization of compounds containing a fatty acid radical
US2421707A (en) * 1945-12-29 1947-06-03 Malkemus John David Mono-substituted dialkanol piperazines

Patent Citations (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US1822108A (en) * 1928-08-07 1931-09-08 Vanderbilt Co R T Stabilization of compounds containing a fatty acid radical
US2421707A (en) * 1945-12-29 1947-06-03 Malkemus John David Mono-substituted dialkanol piperazines

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US3325414A (en) * 1963-10-01 1967-06-13 Colgate Palmolive Co Heavy duty detergent composition containing a quaternary ammonium salt

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