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Publication numberUS3720629 A
Publication typeGrant
Publication date13 Mar 1973
Filing date27 Feb 1970
Priority date27 Nov 1967
Also published asDE1809690A1, DE1809690B2, US3565809
Publication numberUS 3720629 A, US 3720629A, US-A-3720629, US3720629 A, US3720629A
InventorsS Sharman
Original AssigneeChevron Res
Export CitationBiBTeX, EndNote, RefMan
External Links: USPTO, USPTO Assignment, Espacenet
Detergent composition containing hydrogenated alpha olefin sulfonates
US 3720629 A
Abstract  available in
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Claims  available in
Description  (OCR text may contain errors)

iJnitefl States Patent Sharman 1 1March 13, 1973 I DETERGENT COMPOSITION [56] References Cited CONTAINING HYDROGENATED UNITED STATES PATENTS ALPHA OLEFIN SULFONATES 3,506,580 4/l970 Rubinfeld et al. ..252/554 X [75] Inventor: Samuel H. Sharman, Kensington, 3,067,144 12/1962 Michaels ..252/139 Calif. 2,731,422 1/1956 Ross ..252/161 3,384,595 5/1968 Broussalian ..252/l6l Asslgneer Chevron Research p y, San 3,346,629 10/1967 Broussalian ..260 513 Francisco, Calif. 2,746,932 5/1956 Vilate ..252/138 Filed= 27, 9 FOREIGN PATENTS OR APPLICATIONS pp NW 15,214 648,802 4/1964 Belgium Related Apphcatlon Data Primary ExaminerLeon D. Rosdol [62] Division of Ser. No. 685,948, Nov. 27, 1967, Pat. No. Assistant Examiner-P. E. Willis 3,565,809. Att0rneyJ. A. Buchanon, Jr., G. F. Magdeburger,

John Stoner, Jr. and J. T. Brooks [52] US. Cl. ..252/535, 252/536, 252/554,

252/555 [57] ABSTRACT [51] lnt.Cl. ..C1ld3/065,Cl1d1/12 Field of Search "252,161, High performance detergent composmons cons1st of straight-chain hydrogenated olefin sulfonates, an alkali metal or ammonium group pentavalent phosphoric acid salt and an alkanol-l.

7 Claims, No Drawings DETERGENT COMPOSITION CONTAINING IIYDROGENATED ALPIIA OLEF IN SULFONATES CROSS-REFERENCE TO RELATED APPLICATION This application is a division of application Ser. No. 685,948, filed Nov. 27, 1967, now US. Pat. No. 3,565,809.

BACKGROUND OF THE INVENTION 1. Field of the Invention The present invention is concerned with the field of biodegradable sulfonate detergents and more particularly with readily biodegradable olefin sulfonates having improved detersive characteristics.

2. Prior Art Because of the importance of biodegradability, linear alkylbenzene sulfonates now comprise the major active ingredient of household detergents. Although olefin sulfonates are more biodegradable than linear alkylbenzene sulfonates, heretofore, they have not been comparable in terms of detersive characteristics.

The present invention provides novel, readily biodegradable, high performance olefin sulfonate detergent compositions suitable for replacing linear alkylbenzene sulfonates.

SUMMARY OF THE INVENTION Unexpectedly, it has now been found that ternary mixtures of olefin sulfonates containing 11 to 19 carbon atoms, alkali metal or ammonium group pentavalent phosphoric acid salts and alkanol-l compounds containing lO to 15 carbon atoms selected from the normal and 2-methyl isomers possess unusually high detersive characteristics. In particular, the performance of the described ternary mixtures is significantly greater than would be predicted from a knowledge of the performanceof the corresponding binary mixtures or of the components individually. The mechanism by which the olefin sulfonates, alkali pentavalent phosphoric acid salts and alkanols cooperate or interact to produce the improved detersive characteristics is unknown. It is known, however, that all three components are necessary to produce the beneficial effects.

The term olefin sulfonates" as used in the present invention represents a composition consisting of from 50-100 percent unsaturated olefin sulfonates. When the unsaturated olefin sulfonate portion is below approximately 100 percent, the balance of the composition comprises substantially hydroxy sulfonates. Other compounds may also be present in minor amounts due to impurities in olefin feedstock or as the result of sulfonation side reactions. The relative proportions of hydroxy and unsaturated sulfonate will vary depending upon the method of preparation. That is, for example, by one method as described in Turbak, A. F. et al., Reaction of Phosphate-Complex Sulfur Trioxide with Alpha-Olefins," Industrial and Engineering Chemistry, Product Research and Development 2, No. 3, 229 (I963), an olefin sulfonate comprising substantially 100 percent unsaturated olefin sulfonate may be prepared.

Usually, the amount of hydroxy sulfonate will range from to 50 percent by weight of the total olefin sulfonates, and preferably less than 40 percent. The uncarbon atoms. Single carbon cuts of olefins within this range may also be employed, for example, hexadecenel. The olefins may be internal or alpha olefins,

although alpha olefins are preferred. Sulfonation may I be accomplished, by any suitable process which produces the proper range of hydroxy and unsaturated sulfonates.

The preferred method of preparation of olefin sulfonates comprises SO -air sulfonation in a falling film reactor, neutralization and saponification or hydrolysis of the neutralized product. The reaction products of the SO -air sulfonation step may be neutralized with an aqueous alkali solution containing any strongly basic compound such as sodium hydroxide, potassium hydroxide, ammonium hydroxide, the corresponding oxides, carbonates and the like. Sufficient neutralizing solution is added to provide for the subsequent hydrolysis step. Hydrolysis of the neutralized reaction products yields the olefin sulfonates as defined in the present invention.

Generally, the sulfonation conditions cause migration of the double bond in the unsaturated sulfonates and determine the distribution of the double bond locations. Analysis of an alpha olefin C C carbon cut sulfonated with SO -air and suitable for use in the present invention is illustrated in Table I.

TABLE I EUWQQUIAUN OR ONQOQQG "Includes disulfonates Sulfonation also produces a variety of hydroxy sulfonate isomers. Since the beta or Z-hydroxy sulfonates are to some degree insoluble in water, processes which minimize their formation are preferred. A suitable process is described in Marquis et al., Alpha Olefin Sulfonates from a Commercial S0 Reactor, JAOCS, Volume 43, No. 11, pp. 607-614 (1966). British Pat. No. 1,030,648 describes another sulfonation process which may be utilized.

Olefin sulfonates prepared in accordance with the present invention may be modified by mild hydrogenation to produce hydrogenated olefin sulfonates. Hydrogenated olefin sulfonates alone or in mixtures with olefin sulfonates provide excellent active components suitable for the present invention. Hydrogenation of the olefin sulfonates substantially reduces all of the unsaturated sulfonates to alkane sulfonates with little or no effect on the hydroxy sulfonates. The hydrogenation may be conducted with hydrogen at a pressure of 50-800 psig, at a temperature of 45-80C. for 60 minutes over 5% Pd on carbon or barium sulfate as a catalyst.

The primary alkanol component of the detergent composition contains to carbon atoms. The preferred alkanols have the normal or the 2-methyl isomer configuration. Suitable alcohols include decanol-l, undecanol-l, dodecanol-l, tridecanol-l, tetradecanol-l, pentadecanol-l, 2-methyl nonanol, 2- methyl decanol-l, 2-methyl undecanol-l, 2-methyl dodecanol-l, 2-methyl tridecano-l, and 2-methyl tetradecanol. The preferred alkanols may be added separately or in any combination, for example, 75 percent dodecanol-l and 25 percent 2-methyl dodecanol- 1.

The suitable pentavalent phosphoric acid salts include the tripolyphosphates, pyrophosphates, metaphosphates and orthophosphates. The cation portion of the phosphates may be sodium, potassium, ammonium and the like. For example, suitable phosphates would include, but are not limited to: sodium tripolyphosphate, potassium tripolyphosphate, ammonium tripolyphosphate, tetrasodium pyrophosphate, tetrapotassium pyrophosphate, trisodium phosphate, tripotassium phosphate, ammonium phosphate, sodium hexametaphosphate, potassium hexametaphosphate, ammonium hexametaphosphate, monosodium orthophosphate, monopotassium orthophosphate, disodium orthophosphate, dipotassium orthophosphate and the like.

The ternary mixtures of the present invention may be prepared in the usual manner known in the art. The order of combining the ingredients is immaterial. The mixtures so prepared may be utilized as effective detergents if desired. Preferably, however, the detergent compositions of the present invention are incorporated with other ingredients into detergent formulations.

The prescribed quantity of surface active ingredient present in a detergent formulation generally constitutes from about 15 to 35 percent by weight of the total detergent formulation. The olefin sulfonates of the present invention may likewise be utilized in the same concentrations, although preferably from 15 to 25 percent. Correspondingly, the amount of olefin sulfonate employed in a detergent formulation will determine the range of the pentavalent phosphoric acid salt and alkanol-l.

An effective amount of alkali pentavalent phosphoric acid salt usually comprises from about one-fourth to 3 parts by weight per part of olefin sulfonate. Preferably, the ratio is 1 to 2 parts by weight per part of olefin sulfonate.

The selected alkanols or mixtures thereof may comprise from about 4 to 40 parts by weight per hundred parts of olefin sulfonate. The most desirable ratio is usually from 8 to 30 parts by weight per hundred parts of olefin sulfonate.

Additional compatible ingredients may be incorporated into the detergent compositions prepared in accordance with the present invention to enhance their detergent properties. Such ingredients may include, but are not limited to, anticorrosion, antiredeposition, chemical bleaching and sequestering agents; optical whiteners and certain inorganic salts other than phosphate, such as inorganic sulfates, carbonates or borates. The appropriate quantities and compositions of these additives, agents and builders are well described in the art.

An effective means for evaluating the detersive characteristics of detergent compositions is known as the Hand Dishwashing Test which is based on a procedure presented at the ASTM D-l 2 subcommittee on Detergents, mar. 10, 1949, New York N.Y. The test measures under simulated home washing conditionsthe number of plates or dishes washed before the foam collapses. This test 'was utilized to evaluate the improved performance of the disclosed detergent compositions.

Detergent formulations were prepared from the ternary mixtures of the present invention by the addition of water alone or with other ingredients. The formulations were adjusted until the percentage of alcohol and olefin sulfonate equalled 25 percent by weight of the total detergent formulation.

In the following examples, the concentrations employed in the Hand Dishwashing Test were 0.15 percent by weight of the total detergent formulation.

EXAMPLE 1 illustrates a suitable detergent formulation prepared EXAMPLE the ternary mixtures of the present invention.

EXAMPLE 1 A detergent formulation was prepared containing the following percentages of each ingredient, based on the total weight of the formulation:

Ternary Fonnulation Mixture Alpha olefin (C -C sulfonate 21 32 sodium tripolyphosphate 40 62 dodecanol-l 4 6 sodium silicate 7 carboxy methylcellulose 1 sodium sulfate 19 water 8 TABLE II Mixture Composition in Weight Example Phosphate Sulfonate' Dodecanol-l Plates 2 0 0 20 3 0 84 1 6 20 4 28 62 0 1 8 5 44' 56 0 1 7 6 62 3B 0 15 7 62 3 8 0 l8 8 62' 3 8 0 l8 9' 7 1' 29 0 l7 Alpha olefin sulfonate c -c carbon cut As measured by Hand Dishwashing Test" Sodium tripolyphosphate Trisodium phosphate Tetrasodium pyrophosphate Includes inert builders such as sodium silicate, carboxy methyl-cellulose and sodium sulfate Tables Ill and IV represent data obtained from formulations containing all three components. Both tables illustrate the importance of alcohol concentrations on dishwashing ability.

TABLE III Ternary Mixture Composition in Weight Example Phosphate Sulfonate Dodecanol-l 10 28 52 l 22 l l 44 37 9 24 12 62 32 6 23 Sodium tripolyphosphate Alpha olefin sulfonate C -C carbon cut As measured by Hand Dishwashing Test" TABLE IV Ternary Mixture Composition in Weight Example Phosphate Sulfonate Dodecanol-l Plates 1 3 62 26 l2 l5 14 62 28 1O 20 l 5 62 32 6 24 16 62 35 3 22 Tetrasodium pyrophosphate Alpha olefin sulfonate C C carbon out "As measured by Hand Dishwashing Test The changes produced in the dishwashing ability of the present compositions by varying the carbon chain length of the alkanol are shown in Table V.

TABLE V n-Alkanol Example (No. of Carbon Atoms) Plates l7 8 l6 l8 10 23 [9 ll 24 12 24 21 13 23 22 14 21 23 l6 l5 Ternary mixture composition: phosphate 61%; alkanol 6%, olefin sulfonate 33% The dishwashing ability of formulations containing various alcohols is compared with those of the present invention in Table VI Ternary mixture composition; alcohol 6%; phosphate 61%; olefin sulfonate 33% Table V illustrates the dishwashing ability of formulations containing hydrogenated olefin sulfonate alone and in mixtures with olefin sulfonates as the major active components.

TABLE Vll Ternary Mixture Composition in Weight Hydrogenated Olefin Example Dodecanol- Olefin Sulfonate Sulfonate Plates 32 0 3 8 O 25 33 6 32 0 3| 34 0 l9 19 23 35 6 l6 16 28 62% phosphate As will be evident to those skilled in the art, various modifications on this process can be made or followed, in the light of the foregoing disclosure and discussion, without departing from the spirit or scope of the disclosure or from the scope of the following claims.


l. A detergent composition having improved detersive characteristics consisting essentially of normal alkali metal and ammonium hydrogenated olefin sulfonates produced by sulfonating straightchain olefines containing 11 to 19 carbon atoms with S0 neutralizing the resulting mixture with an alkali metal or ammonium hydroxide, carbonate or oxide, hydrolyzing the neutralized product, and subsequently hydrogenating the hydrolyzed product to substantially reduce all of the unsaturated olefin sulfonates to alkane sulfonates, said hydrogenated product consisting essentially of a mixture of alkane and hydroxy alkane sulfonates,

an alkali metal or ammonium pentavalent phosphoric acid salt in a ratio of about one-fourth to 3 parts per part by weight of sulfonate, and

an alkanol-l containing 10 to 15 carbon atoms selected from the class consisting of the normal and Z-methyl isomers in a ratio of about 4 to 40 parts per hundred parts by weight of sulfonate.

2. A detergent composition according to claim 1, wherein the alkanol-l is dodecanol-l 3. A detergent composition according to claim 2, wherein the phosphoric acid salt is selected from the group consisting of sodium tripolyphosphate, tetrasodium pyrophosphate and trisodium phosphate. I

4. A detergent composition according to claim 3, wherein the phosphoric acid salt is present in a ratio of about 1 to 2 parts per part by weight of sulfonate.

5. A detergent composition according to claim 4, wherein the alkanol-l is present in a ratio of about 8 to 30 parts per hundred parts by weight of sulfonate.

6. A detergent composition according to claim 5, wherein the alkanol-l is composed of a mixture of the normal and 2-methyl isomers.

7. A detergent composition according to claim 5, wherein the hydrogenated olefin sulfonate is derived from an alpha olefin cut containing 15 to 18 carbon atoms.

Patent Citations
Cited PatentFiling datePublication dateApplicantTitle
US2731422 *18 Oct 194917 Jan 1956Colgate Palmolive CoNon-soap detergent compositions
US2746932 *8 Oct 194922 May 1956Colgate Palmolive CoSynthetic detergent compositions
US3067144 *16 Nov 19594 Dec 1962Stamford Chemical Ind IncDetergent composition
US3346629 *15 Aug 196310 Oct 1967Monsanto CoProcess for preparing beta-ethylenically unsaturated organic sulfonates
US3384595 *15 Dec 196421 May 1968Monsanto CoDetergent compositions containing gamma-hydroxy organic sulfonate type compounds
US3506580 *10 May 196614 Apr 1970Colgate Palmolive CoHeat-treatment of sulfonated olefin products
BE648802A * Title not available
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US5476614 *17 Jan 199519 Dec 1995Colgate Palmolive Co.High foaming nonionic surfactant based liquid detergent
US5565420 *6 Jun 199515 Oct 1996The Procter & Gamble CompanyGranular detergent composition containing admixed fatty alcohols for improved cold water solubility
US5767050 *11 Oct 199516 Jun 1998Colgate-Palmolive Co.Light duty liquid cleaning compositions comprising partially esterified polyhydric alcohol solubilizing agent
US5840676 *17 Jul 199724 Nov 1998Colgate-Palmolive CompanyMicroemulsion light duty liquid cleaning compositions
US5853743 *5 Aug 199729 Dec 1998Colgate Palmolive CompanyLight duty liquid cleaning compositions
US5866529 *20 Sep 19962 Feb 1999Colgate-Palmolive CoHigh foaming nonionic surfactant base liquid detergent comprising gelatin beads
WO1995031525A1 *17 Apr 199523 Nov 1995The Procter & Gamble CompanyGranular detergent composition containing admixed fatty alcohols for improved cold water solubility
U.S. Classification510/497, 510/235
International ClassificationC11D3/065, C11D1/14, C11D3/20
Cooperative ClassificationC11D1/143, C11D3/2013, C11D3/065
European ClassificationC11D3/20B1A2, C11D3/065, C11D1/14B