US3709838A

US3709838A - Liquid detergent compositions

Info

Publication number: US3709838A
Application number: US00091153A
Authority: US
Inventors: M Mausner; A Dater
Original assignee: Witco Chemical Corp
Current assignee: Witco Corp
Priority date: 1965-11-29
Filing date: 1970-11-19
Publication date: 1973-01-09
Anticipated expiration: 1990-01-09
Also published as: DE1543970B2; FR2207980A2; CA983806A; FR1501661A; DE2355402A1; US3856711A; FR2207980B2; GB1114359A; BE807519A; GB1455283A; BE805077Q; DE1543970A1; DE2355402C3; DE2355402B2

Abstract

POLYFUNCTIONAL ESSENTIALLY 100% ACTIVE STABLE LIQUID DETERGENT COMPOSITIONS CONSISTING ESSENTIALLY OF (A) FROM 30 TO 90% OF AN ETHANOLAMINE SALT OF A C8 TO C18 ALKYL BENZENE- OR ALKYL TOLUENE-SULFONIC ACID, (B) FROM 5 TO 35% OF A NONIONIC NORMALLY LIQUID, WATER-SOLUBLE SURFACTANT IN THE FORM OF AN ETHOXYLATED OR PROPOXYLATED ETHER OF (i) AN ALIPHATIC MONOHYDRIC ALCOHOL CONTAINING AT LEAST 8 CARBON ATOMS OR (ii) AN ALKYL PHENOL IN WHICH THE ALKYL RADICAL CONTAINS A TOTAL OF FROM 5 TO 18 CARBON ATOMS AND (C) FROM 5 TO 35% OF A C10 TO C16 FATTY ACID MONOETHANOLAMIDE, DIETHANOLAMIDE OR MONOISOPROPANOLAMIDE.

Description

United States Patent 3,709,838 LIQUID DETERGENT COMPOSITIONS Marvin L. Mausner, Teaneck, and Arnold H. Dater, Fair Lawn, N.J., assignors to Witco Chemical Corporation, New York, N.Y.

No Drawing. Continuation-impart of application Ser. No. 777,143, Nov. 19, 1968, which is a continuation-in-part of application Ser. No. 510,358, Nov. 29, 1965, both now abandoned. This application Nov. 19, 1970, Ser. No. 91,153

Int. Cl. Clld 1/18, 3/32, 7/32 U.S. Cl. 252545 19 Claims ABSTRACT OF THE DISCLOSURE Polyfunctional essentially 100% active stable liquid detergent compositions consisting essentially of (a) from 30 to 90% of an ethanolamine salt of a C to C alkyl benzeneor alkyl toluene-sulfonic acid, (b) from to 35% of a nonionic normally liquid, water-soluble surfactant in the form of an ethoxylated or propoxylated ether of (i) an aliphatic monohydric alcohol containing at least 8 carbon atoms or (ii) an alkyl phenol in which the alkyl radical contains a total of from 5 to 18 carbon atoms, and (c) from 5 to 35% of a C to C fatty acid monoethanolamide, diethanolamide or monoisopropanolamide.

This application is a continuation-in-part of application Ser. No. 777,143, filed Nov. 19, 1968, now abandoned, which is a continuation-in-part of application Ser. No. 510,358, filed Nov. 29, 1965, now abandoned.

This invention is directed to new and useful anhydrous or essentially anhydrous liquid surfactant compositions, and more particularly to polyfunctional liquid detergent compositions that comprise essentially 100% active organic surfactants and to a method of making them.

The production and marketing of polyfunctional detergent compositions has been known for a number of years and numerous formulations have been evolved. Various combinations of surfactant materials have been prepared in a wide range of concentrations to modify the properties of the detergent compositions in a desired manner. These combinations are disclosed in numerous US. patents, illustrative of which are Nos. 2,383,737; 2,733,- 213; 2,733,214; 2,746,931; 2,826,596; 2,831,815; 2,846- 402; 3,075,922 and 3,239,468.

It is known in the detergent art to prepare polyfunctional detergent compositions in powdered or flake form, such as obtained by the spray-drying or drum-drying of a slurry of a detergent composition, that contain a high concentration of active organic surfactant materials, i.e., as high as 90% of active surfactant material. It has also been suggested, as disclosed in the afore-mentioned US. Pat. No. 3,239,468, to prepare detergent compositions comprising certain proportions of alkyl aryl sulfonates, nonionic polyoxyethylene alkylphenol condensates and fatty acid-diethanolamine condensates without any added water or other vehicle, such as a liquid medium, and subsequently diluted to use concentrations, or subsequently admixed with a liquid medium. In point of fact, in the actual working example disclosures of said Pat. No. 3,239,468, aqueous slurries of the alkyl aryl sulfonates are utilized and, in Example 1 of said patent, which describes a detergent composition produced in the absence of either a liquid medium or water as added diluent, a very considerable amount of water is actually present, namely, about 16% of the total composition. Furthermore, as there disclosed, the alkyl aryl sulfonates, such as dodecylbenzene sulfonate, can be utilized in the form of their alkali metal, ammonium or alkanolamine salts.

When the procedures described in said patent, utilizing the proportions of the various ingredients disclosed therein, are, however, sought to be applied to the production of essentially active stable liquid detergent compositions, such compositions are, in fact, characterized by poor clarity and substantial instability, separating into layers after even quite short periods of standing. So far as we are aware, the preparation of polyfunctional organic detergent compositions in the form of stable, homogeneous liquids, generally speaking, has been limited to solutions having a concentration of active organic surfactant materials of the order of 50 to 70%. While it is highly desirable from an economy standpoint to prepare polyfunctional detergent compositions in liquid form which are stable over prolonged periods of time, and in which the content of the active organic surfactants approaches 100%, when attempts are made to produce such compositions, various problems arise.

One of such problems in the production of essentially 100% active, stable polyfunctional liquid detergent compositions is the matter of instability. This instability may be evidenced by the formation of two or more immiscible phases either during the preparation of the detergent composition or on standing over short periods of time. Another of such problems is the production of such a detergent composition which will, upon dilution with water in certain concentrations, where such dilution may be desired, dissolve readily and operate to perform effectively its desired detergent functions.

In accordance with the present invention, it has been found that a 100% active, or essentially 100% active, or essentially anhydrous polyfunctional organic detergent composition in the form of a clear, homogeneous, stable liquid can be prepared by a certain balancing of a number of essential ingredients, and advantageously employing a particular mixing or blending procedure.

The essentially anhydrous liquid polyfunctional organic detergent compositions of the present invention contain as essential ingredients, in the ranges of proportions set forth hereafter, (1) ethanolamine (i.e., monoethanolamine, diethanolamine and triethanolamine or mixtures of two or more thereof) salts of alkyl benzene sulfonic acids or alkyl toluene sulfonic acids, particularly the diethanolamine or triethanolamine salts of said sulfonic acids (2) certain ethanolamides or isopropanolamides, and (3) certain water-soluble nonionic organic detergents which are normally liquid or, in other words, liquid at usual room temperatures.

The alkyl benzene sulfonic acids and the alkyl toluene sulfonic acids, which are utilized in the form of their ethanolamine salts as stated above, are those in which the alkyl radical, which may be linear or branched chain, contains predominately from 8 to 16 carbon atoms and, better still, from 11 to 15 carbon atoms. Especially satisfactory are dodecyl benzene sulfonic acid and tridecyl benzene sulfonic acid, as well as mixtures thereof or mixtures in which one or the other or both predominate, in which the dodecyl and tridecyl radicals are essentially normal or straight chain. The alkyl benzene or alkyl toluene sulfonic acids are well known in the art and are conventionally made by alkylating benzene or toluene with normal or straight chain chloroparaffins, polypropylenes, or olefins, although other sources of alkyl radicals can, of course, be utilized. The ethanolamine salts of the aforesaid sulfonic acids are formed and incorporated in the manner described below. It may be noted that it is important to the achievement of the results of the present invention, taken in conjunction with the other essential aspects of the invention, not only to utilize ethanolamine salts of the aforesaid sulfonic acids, because the alkali metal salts are not operative,

but, in addition, that said ethanolamine salts be formed in situ. It may also here be noted that many alkanolamines are unsatisfactory for the purposes of our present invention. Furthermore, to achieve the optimum advantages of the present invention, said in situ formation should be carried out in the manner hereafter described as a part of the overall method of blending the ingredients to form the final liquid detergent compositions of the present invention. It may be stated that, in itself, in situ formation, broadly, of ethanolamine salts of alkyl benzene sulfonic acids as a part of a procedure for producing liquid detergent compositions is known to the art and no claim is made generally thereto. However, in such cases, the in situ formation of ethanolamine salts of alkyl benzene sulfonic acids has occurred in connection with the production of liquid detergent compositions containing substantial quantities of water, for instance, about 35 to 50%, as an essential part of the liquid detergent compositions, as shown, for example, in US. Pat. No. 3,232,880 and in Australian Pat. No. 164,644. In any event, and as pointed out above, our present invention and our polyfunctional essentially 100% active stable liquid detergent compositions are sharply distinguishable therefrom.

The normally liquid water-soluble non-ionic surfactants which are utilized in the liquid detergent compositions of the present invention serve as primary surfactants as well as liquid carriers. They are, per se, well known and are exemplified mainly by ethylene oxide adducts or polyethenoxy ethers of (i) aliphatic monohydric alcohols, comprising straight chain and branched chain saturated and unsaturated alcohols containing at least 8 carbon atoms and generally up to 18 carbon atoms, particularly branched chain and fatty alcohols containing from 10 to 14 carbon atoms or (ii) alkyl phenols, particularly monoor di-alkyl phenols, in which the alkyl radicals contain a total of from 5 to 18 carbon atoms, especially mono-alkyl phenols in which the akyl radical contains from 8 to 12 carbon atoms. The mol ratio of the ethylene oxide to the aforesaid alcohols or alkyl phenols in the adducts is variable within quite wide limits, generally being at least 4 to 20 or more mols of ethylene oxide to 1 mol of said alcohols or alkyl phenols, especialy 6 to mols of ethylene oxide to 1 of said alcohols or alkyl phenols. In general, the especially desirable normally liquid non-ionic organic surfactants utilized will be the 6 to 10 mol ethylene oxide adducts of (i) straight chain or branched chain aliphatic monohydric alcohols or (ii) mono-alkyl phenols in which the alkyl radical contains from 8 to 12 carbon atoms.

The ethanolamides and/or isopropanolamides, which serve as viscosity builders and foam boosters in the liquid detergent compositions of the present invention, are the fatty acid monoethanolamides, diethanolamides and isopropanolamides in which the fatty acid acyl radical contains from 10 to 16 carbon atoms. Said amides should be either normally liquid or have melting points not higher than about 60 degrees C. Especially satisfactory are the diethanolamides derived from coconut oil mixed fatty acids or special fractions containing, for instance, very predominately C or C fatty acids, and wherein the mol ratio of the diethanolamine to the higher fatty acid is about 1: 1.

The proportions of the ingredients, in terms of weight percent, comprising the liquid detergent compositions of the present invention are (A) from 30 to 90%, better still 45 to 75%, of the aforementioned ethanolamine salts of the alkyl benzeneor alkyl toluene-sulfonic acids, (B) from 5 to 35%, better still 15 to of the aforementioned non-ionic normally liquid, water-soluble surfacants, and (C) from 5 to better still 12 to 25 %,of the aforementioned fatty acid amides of monoethanolamine, diethanolamine or isopropanolamine. Particularly desirable are liquid detergent compositions made pursuant to the present invention wherein the aforesaid ethanolamine salts of the alkyl benzeneor alkyl toluene-sulfonic acid constitute from 52 to 64%, the aforesaid non-ionic surfactant constitutes from 22 to 30%, and the aforesaid fatty acid monoor diethanolamides or isopropanolamides constitute from 14 to 18% of the compositions.

In the preparation of the polyfunctional essentially active stable liquid detergent compositions of the present invention, it is particularly advantageous first to form a substantially homogeneous solution of the nonionic normally liquid water-soluble surfactant with an ethanolamine and then gradually add thereto, under conditions of agitation, the alkyl benzene sulfonic acid and/ or alkyl toluene sulfonic acid in an amount essentially to be neutralized by said ethanolamine thereby to form the ethanolamine salt of said sulfonic acid, the temperature of the mixture being controlled so as not to exceed about 100 C. and preferably not to substantially exceed 50 C., and then add the ethanolamide and/or isopropanolamide, under conditions of agitation, until a clear, homogeneous liquid is obtained. An alternative procedure is first to form a mixture of the non-ionic surfactant and the sulfonic acid and then gradually add thereto the ethanolamine under conditions of agitation. Still other procedures can be used but the non-ionic surfactant must comprise the vehicle in which in situ formation of the ethanolamine salt of the sulfonic acid is effected. Thus, for instance, stable compositions cannot be formed if the ethanolamine salt of the sulfonic acid is sought to be formed in situ in the ethanolamide and/or isopropanolamide per se. As indicated, nonionic surfactant must be present during the in situ formation of the ethanolamine salt of the sulfonic acid.

It may also be noted that the polyfunctional essentially 100% active stable liquid detergent compositions of the present invention cannot be made by initially preparing an aqueous solution of the active ingredients and then evaporating off the water because, among other things, at a concentration of about 60% of the active ingredients, breakdown of the composition occurs and instability resu ts.

The following examples include illustrative or particularly preferred embodiments of the present invention, but they are not to be construed as in any way limitative of the invention since numerous other embodiments can readily be evolved in the light of the guiding principles and teachings provided herein. All parts recited are by weight.

Example 1 To 26 parts of the condensation product or adduct of 6 mols of ethylene oxide and 1 mol of a linear fatty alcohol having mainly 10 to 14 carbon atoms there was added 20 parts of diethanolamine. Then 40 parts of dodecyl benzene sulfonic acid (88% minimum activity) was slowly added, under conditions of agitation, the temperature of the reactants and the reaction mixture being maintained below 50 C. and, better still, between about 20 and 30 C. The forementioned amount of diethanolamine is the stoichiometric quantity required to neutralize the dodecyl benzene sulfonic acid. When the neutralization was complete, 14 parts of a superamide (made from 1 mol of coconut oil fatty acids and 1 mol of diethanolamine) was added, under conditions of agitation, until a clear, homogeneous liquid was obtained.

The properties of said liquid detergent composition, hereinabove prepared, were as follows:

Appearance: Clear amber liquid Water content: Less than 2% Cloud point: Less than 0 C. Clear point: Less than 0 C.

The stability of said liquid detergent compositions was excellent, no separation of ingredients occurring after several months of aging at ambient temperatures and also at 0 C.

The above procedure, when conducted at temperatures of as high as 100 C., or even higher, results in detergent compositions which are progressively slightly darker as the temperature of the reaction increases. The darker compositions, prepared according to the present invention, are utilized when the end use thereof is not affected by the darker colors or wherein darker colored compositions are preferred. The efiicacy and utility of the detergent compositions is, however, not affected by such color considerations.

The following table illustrates the slight degree of darkening of the final liquid detergent compositions as the temperature is increased. Readings were made on a Klett-Summerson Photoelectric Colorimeter. Readings were made immediately after neutralization and one hour after neutralization at the temperature indicated, to simulate conditions in the processing of large batches which would be difiicult to cool rapidly.

Klett color Klett color after after one addition hour Viscosity, cps. at

Solution concentration, percent These results demonstrate the unique viscosity building properties of the liquid detergent compositions of the present invention when mixed with water. They also point up the importance and criticality of excluding water during the preparation of the compositions of the present invention. Finally, and in this same connection, they emphasize the unexpectedness of our invention since it would have been assumed that any effort by those skilled in the art to make compositions such as ours would have resulted in gels. We found, however, surprisingly, that polyfunctional essentially 100% active liquid detergent compositions of the type here involved could be made which are stable and readily pourable.

Example 1(a) In sharp contrast to the results obtained in Example 1, when a detergent composition was sought to be made by simply mixing together 26 parts of the same 6-mo1 ethylene oxide adduct used in Example 1, 14 parts of the same superamide used in Example 1, and 60 parts of the sodium salt of dodecyl benzene sulfonic acid active, or in the form of an aqueous slurry as in the aforesaid Pat. No. 3,239,468), the resulting composition was unclear and unstable and quickly formed separate layers, including undissolved material.

Example 1 (b) Again, when an essentially anhydrous detergent composition was sought to be made by simply admixing together 26 parts of the same 6-mol ethylene oxide adduct used in Example 1, 14 parts of the same superamide used in Example 1, and 60 parts of a preformed diethanolamine salt of dodecyl benzene sulfonic acid made by admixing 20 parts of diethanolamine with 40 parts of dodecyl benzene sulfonic acid (88% minimum activity), an extremely non-homogeneous, unclear composition resulted in which solids readily separated out. Indeed, a usable preformed diethanolamine salt of dodecyl benzene sulfonic acid could not be made because an unmanageable gel resulted on mixing diethanolamine with dodecyl benzene sulfonic acid.

Example 1(c) A detergent composition was sought to be made y simply admixing together 30 parts of a IO-mol ethylene oxide adduct of nonylphenol, 50 parts of a coconut fatty acid-diethanolamine condensate (mol ratio of coconut fatty acidszdiethanolamine being 1:1), and 20 parts of the sodium salt of dodecyl benzene sulfonic acid (100% active or in the form of an aqueous slurry as in the aforesaid Pat. No. 3,239,468). The resulting composition was unclear and unstable, readily separating out into layers.

Example 1(d) A detergent composition was sought to be made by simply admixing together 30 parts of a 10-mol ethylene oxide adduct of nonylphenol, 50 parts of a coconut fatty acid-diethanolamine condensate (mol ratio of coconut fatty acids:diethanolamine being 1:1), and 20 parts of a preformed diethanolamine salt of dodecyl benzene sulfonic acid. The resulting composition was extremely nonhomogeneous and unclear from which solids readily separated out. (Note the observations made in Example 1(b) regarding the matter of seeking to prepare the preformed diethanolamine salt of dodecyl benzene sulfonic acid.)

Examples 1(c) and 1(d) are illustrative of compositions falling within the ranges of proportions of the stated ingredients disclosed in the aforesaid Pat. No. 3,239,468 sought to be made simply by mixing together said ingredients. These examples, as well as Examples 1(a) and 1(b), show that our polyfunctional essentially 100% active stable liquid detergent compositions are not obtainable by following the procedures described in said Examples 1(a), 1(b), 1(c) and 1(d).

Example 2 Parts Diethanolamine 20 Linear dodecyl benzene sulfonic acid (88% active) 40 6-mol ethylene oxide adduct of C C fatty alcohols 18 Coconut oil fatty acid diethanolamide (1:1 mol ratio) 22 Example 3 Parts Triethanolamine 25 Linear dodecyl benzene sulfonic acid (88% active) 35 9-mol ethylene oxide adduct of octyl phenol 22 Laurie acid diethanolamide (1:1 mol ratio) 18 Example 4 Diethanolamine 14 Alkyl benzene sulfonic acid (98% active-branched chain alkyl radical containing predominately 11 carbon atoms) 41 6-mol ethylene oxide adduct of IZ-carbon atom secondary alcohol 30 Coconut oil fatty acid diethanolamide 1:1 mol ratio) v- 15 Example Parts Diethanolarnine 2O Branched chain dodecyl benzene sulfonic acid (88% active) 30 Branched chain mixed C C alkyl benzene sulfonic acids (88% active) 10 6-mo1 ethylene oxide adduct of C fatty alcohol 26 Coconut oil fatty acid diethanolamide (1:1 mol ratio) 14 Example 6 Parts Diethanolamine Linear tridecyl benzene sulfonic acid 4O 8-mol ethylene oxide adduct of nonyl phenol 24 Laurie acid diethanolamide (1:1 mol ratio) 16 Example 7 Parts Diethanolamine 20 Linear dodecyl benzene sulfonic acid (88% active) 40 7-mo1 ethylene oxide adduct of n-dodecyl alcohol 25 Coconut oil fatty acid diethanolamide (1: 1.1) 15 The compositions of Examples 27 are made in the manner described in Example 1. They are all clear stable liquids under ambient conditions as well as at 0 C.

The liquid detergent compositions of the present invention, as pointed out above, are 100% active essentially 100% active. In the preparation of said compositions, it is advisable, for optimum results, that no water be deliberately added during such preparation. However, some water may enter into the final liquid detergent compositions by reason of its presence in small proportions in one or more of the ingredients utilized in the preparation of said compositions. In any event, the method of preparation and the selection of ingredients should so be controlled that the water content of the final liquid detergent compositions does not exceed 2% of the total weight of said liquid detergent compositions. Where reference is made in the claims to essentially 100% active stable liquid detergent composition, it will be understood that said compositions may contain up to 2% water.

The liquid detergent compositions of the present invention, in addition to exhibiting excellent cleaning power for many commercial and consumer requirements including hard surface cleaning, have the important advantages of providing essentially 100% organic surfactant activity with the accompanying economic advantages in shipping and storing, and outstanding stability over prolonged periods of time over a wide temperature range. Said liquid detergent compositions are readily pourable or pumpable, and they can be diluted with water to various commercially acceptable concentrations, forming aqueous solutions which are also stable over a wide temperature range and for extended periods of time.

We claim:

1. In a method of making a polyfunctional essentially 100% active stable liquid detergent composition consisting essentially of the following ingredients in the following percentages by weight:

Percent (A) An ethanolamine salt of a member selected from the group consisting of alkyl benzeneand alkyl toluene-sulfonic acids in which the alkyl radical contains from 8 to 18 carbon atoms (B) Non-ionic normally liquid, water soluble surfactant in the form of a member selected from the group consisting of (i) ethoxylated aliphatic monohydric alcohols containing from 8 to 18 carbon atoms and (ii) ethoxylated alkyl phenols in which the alkyl radicals are l to 2 in number and contain a total of from 5 to 18 carbon atoms, subject to the proviso that the number of rnols of ethylene oxide in said surfactant is in the range of about 4 to about 20 mols per mol of said alcohols or alkyl phenols, as the case may be (C) Fatty acid amides selected from the group consisting of monoethanolamide, diethanolamide and isopropanolamide in which the fatty acid acyl radical contains from 10 to 16 carbon atoms the steps which comprise forming a substantially homogeneous solution of the (B) ingredient with an ethanolamine, then gradually adding thereto, under conditions of agitation, a member selected from the group consisting of alkyl benzeneand alkyl toluene-sulfonic acids in which the alkyl radical contains from 8 to 18 carbon atoms, said sulfonic acid being added in an amount essentially to be neutralized by said ethanolamine thereby to form the ethanolamine salt of said sulfonic acid, the temperature of the above mixture being maintained so as not to exceed about C., and then adding, under conditions of agitation, said (C) ingredient until a clear, homogeneous liquid is obtained.

2. In a method of making a polyfunctional essentially 100% active stable liquid detergent composition consisting essentially of the following ingredients in the following percentages by weight:

Percent (A) An ethanolamine salt of a member selected from the group consisting of alkyl benzeneand alkyl toluene-sulfonic acids in which the alkyl radical contains from 8 to 18 carbon atoms (B) Non-ionic normally liquid, water soluble surfactant in the form of a member selected from the group consisting of (i) ethoxylated aliphatic monohydric alcohols containing from '8 to 18 carbon atoms and (ii) ethoxylated alkyl phenols in which the alkyl radicals are 1 to 2 in number and contain a total of from 5 to 18 carbon atoms, subject to the proviso that the number of mols of ethylene oxide in said surfactant is in the range of about 4 to about 20 mols per mol of said alcohols or alkyl phenols, as the case may be (C) Fatty acid amides selected from the group consisting of monoethanolamide, diethanolamide and isopropanolamide in which the fatty acid acyl radical contains from 10 to 16 carbon atoms the steps which comprise forming a substantially homogeneous solution of the (B) ingredient with a member selected from the group consisting of alkyl benzeneand alkyl toluene-sulfonic acids in which the alkyl radical contains from 8 to 18 carbon atoms, then gradually adding thereto, under conditions of agitation, an ethanolamine, said ethanolamine being added in an amount essentially to be neutralized by said sulfonic acid thereby to form the ethanolamine salt of said sulfonic acid, the temperature of the above mixture being maintained so as not to exceed about 100 C., and then adding, under conditions of agitation, and (C) ingredient until a clear, homogeneous liquid is obtained.

3. A method according to claim 1, wherein the temperature is maintained at below 50 C.

4. A method according to claim 1, wherein the (B) ingredient is a 6 to mol ethylene oxide adduct of a member selected from the group consisting of (i) a fatty alcohol containing from 10 to 14 carbon atoms and (ii) an alkyl phenol in which the number of alkyl radicals is from 1 to 2 and the total number of carbon atoms in said alkyl radicals is between 8 and 12, and wherein the alkyl radical of said sulfonic acid contains predominately from I 11 to carbon atoms.

5. A method according to claim 1, wherein the sulfonic acid is a member selected from the group consisting of dodecyland tridecyl-benzene sulfonic acid, and the (B) ingredient is a 6 to 10 mol ethylene oxide adduct of a member selected from the group consisting of (i) a C -C fatty alcohol and (ii) a C to C alkyl phenol.

6. A method according to claim 5, wherein the (B) ingredient constitutes from 22 to 30%, the (C) ingredient constitutes from 14 to 18%, and the ethanolamine salt of the sulfonic acid constitutes from 52 to 64% of the finished liquid detergent composition.

7. A method according to claim 1, wherein the (A) ingredient constitutes 45 to 75%, the (-B) ingredient constitutes 15 to 30%, and the (C) ingredient constitutes 12 to 8. A method according to claim 4, wherein the (A) ingredient constitutes 45 to 75%, the (B) ingredient constitutes 15 to and the (C) ingredient constitutes 12 to 25 9. A method according to claim 1, wherein the (A) ingredient is an ethanolamine salt of a member selected from the group consisting of dodecyland tridecylbenzene sulfonic acid, the (B) ingredient is a 6 to 10 mol ethylene oxide adduct of a member selected from the group consisting of (i) a C -C fatty alcohol and (ii) a C to C mono-alkyl phenol, and the (C) ingredient is a C -C fatty acid diethanolamide.

10. A method according to claim 9, wherein the (A) ingredient constitutes from 52-64%, the (B) ingredient constitutes from 22 to 30%, and the (C) ingredient constitutes from 14 to 18%.

11. A method according to claim 9, wherein the (A) ingredient is a diethanolamine salt of a linear tridecyl benzene sulfonic acid, and the (B) ingredient is an approximately 7 mol ethylene oxide adduct of n-dodecyi alcohol.

12. A method according to claim 9, wherein the (A) ingredient is a diethanolamine salt of a linear dodecyl benzene sulfonic acid, and the (B) ingredient is an approximately 7 mol ethylene oxide of n-dodecyl alcohol.

13. A method according to claim 2, wherein the temperature is maintained at below 50 C.

14. A method according to claim 2, wherein the (B) ingredient is a 6 to 10 mol ethylene oxide adduct of a member selected from the group consisting of (i) a fatty alcohol containing from 10 to 14 carbon atoms and (ii) an alkyl phenol in which the number of alkyl radicals is from 1 to 2 and the total number of carbon atoms in said alkyl radicals is between 8 and 12, and wherein the alkyl radical of said sulfonic acid contains predominately from 11 to 15 carbon atoms.

15. A method according to claim 14, wherein the (B) ingredient constitutes from 22 to 30%, the (C) ingredient constitutes from 14 to 18%, and the ethanolamine salt of the sulfonic acid constitutes from 52 to 64% of the finished liquid detergent composition.

16. A method according to claim 2, wherein the (A) ingredient constitutes 45 to the (B) ingredient constitutes 15 to 30%, and the (C) ingredient constitutes 12 to 25%.

17. A method according to claim 14, wherein the (A) ingredient constitutes 45 to 75%, the (B) ingredient constitutes 15 to 30%, and the (C ingredient constitutes 12 to 25% 18. The product produced by the method of claim 1.

19. The product by the method of claim 2.

References Cited UNITED STATES PATENTS 3,239,468 3/ 1966 Herrick 252-548 3,549,544 12/1970 Johnson 252-152 2,859,182 11/1958 Carroll 252-137 OTHER REFERENCES Milwidsky, B.: Liquid Synthetic Detergents Soap and Chemical Specialties (April 1963), pp. 53-56.

J MAYER WEINBLATT, Primary Examiner E. ROLLINS, Assistant Examiner US. Cl. X.R.