FIELDOFTHE INVENTION

The present invention is generally directed to a process for making a granular detergent composition having improved solubility in cold temperature laundenng solutions More particularly, the invention is directed to a process duπng which a hydrotrope selected from the group consisting of sulfyl succinates, xylene sulfonates, cumene sulfonates and mixtures thereof is mixed with a sulfated surfactant selected from the group consisting of alkyl sulfates (also referenced herein as "AS"), alkyl ethoxy sulfates (also referenced herein as "AES"), and secondary alkyl sulfates (also referenced herein as "SAS") and mixtures thereof, to form a paste The paste and other adjunct detergent ingredients including a builder are agglomerated to form a high density compact detergent composition having improved solubility in cold temperature washing solutions (e g 5°C to 30°C) and high water hardness conditions (e g 7 grams gallon)

BACKGROUND OF THE INVENTION Typically, conventional detergent compositions contain mixtures of vaπous surfactants in order to remove a wide variety of soils and stains from surfaces For example, vaπous anionic surfactants, especially the alkyl benzene sulfonates, are useful for removing paniculate soils, and 0 vanous nonionic surfactants, such as the alkyl ethoxylates and alkylphenol ethoxvlates, are useful for removing greasy soils

While the art is replete with a wide variety of surfactants for those skilled in the art of detergent formulation, most of th available surfactants are specialty chemicals which are not suitable for routine use in low cc ms such as home laundenng compositions The fact remains 5 that many home-use laundry detergents still compπse one or more of the conventional alkyl benzene sulfonates or pnmary alkyl sulfate surfactants Another class of surfactants which has found use in vanous compositions where emulsification is desired compπses the secondary alkyl sut ^f ates The conventional secondary alkyl sulfate surfactants are available as generally pa ^c * random mixtures of sulfated linear and/or partially branched alkanes 0 For example, Rossall et al. U S Patent No 4,235,752, disclose a detergent surfactant which is a CJO-18 secondary alkyl sulfate containing 50% of 2/3 sulfate isomers and 40% of vaπous other effective isomers The surfactant mateπals disclosed by Rossall et al is for use pπmaπly in dishwashing operations Such mateπals have not come into widespread use in laundry detergents, since they do not offer any advantages o\er alkvl benzene sulfonates especially with respect to 5 water solubility which facilitates production of high-surfactant granular detergents Accordingly Rossall et al do not provide a high density laundry detergent having improved solubility in either cold temperature wash solutions or high hardness water conditions

The limited solubility of alkyl sulfate surfactants including both primary and secondary alkyl sulfates is especially prevalent in modern granular laundry detergents which are typically used in cold temperature (e.g. 5°C to 30°C) washing solutions and are formulated in "condensed" or "compact" form for low dosage usage. For the consumer, the smaller package size attendant with compact detergent products provides for easy storage and handling. For the manufacturer, unit storage costs, shipping costs and packaging costs are lowered.

The manufacture of acceptable compact or condensed granular detergents has its difficulties. In a typical compact detergent formulation, the so-called "inert" ingredients such as sodium sulfate are substantially eliminated. However, such ingredients do play a role in enhancing solubility of conventional detergents. As a consequence, compact detergents often suffer from solubility problems, especially in cold temperature laundering solutions. Moreover, conventional compact or low density detergent granules are usually prepared by spray drying processes which result in extremely porous detergent particles that are quite amenable to being dissolved in aqueous washing solutions. By contrast, compact detergents are typically comprised of less porous, high density detergent particles which are less soluble, e.g. agglomerates. Thus, since the compact form of granular detergents typically comprise particles or granules which contain high levels of detersive ingredients with little or no room for solubilizing agents, and since such particles are intentionally manufactured at high bulk densities, the net result can be a substantial problem with regard to in- use solubility. In the art of detergency, the use of hydrotropes have generally been associated with liquid detergent compositions to increase the solubility of various detergent ingredients in the composition. For example, Gutierrez et al, U.S. Patent No. 4,528, 144 (Lever), is directed to a liquid detergent compositions containing terpene sulfonate hydrotropes and various other detergent ingredients. In a similar fashion, Lamberti et al, U.S. Patent No. 4,623,483 (Lever), is also directed to a liquid detergent composition comprising a hydrotrope and other conventional detergent ingredients. Both of the Lamberti et al and Gutierrez patents only suggest processes for making "liquid" compositions and are silent with respect to processing granular or agglomerated versions of the detergent disclosed therein. Thus, these patents do not speak to the solubility problem associated with cold temperature laundering solutions, a problem particularly prevalent when using detergents which are not spray-dried.

Accordingly, despite the disclosures in the art, there remains a need for a process for making a detergent composition which has improved solubility, especially in cold temperature washing solutions. This need is especially prevalent in the art of compact or high density detergents currently being used by consumers. There is also a need for such a process which produces a detergent composition having improved solubility under high water hardness conditions. Also, there is a need for such a process resulting in a detergent composition having improved biodegradability.

SUMMARY OF THE INVENTION The pre nvention meets the needs identified bv pro iding a process for making a detergent composu.-->n in the ftr ^r agglomerates which exhibit improved solubilitv or dissolution of the anionic surfactants in co .perature washing solutions as well as under high water hardness conditions The process .ncludes the step of mixing a high level of a sulfated surfactant selected from the group of alkyl sulfates, alky 1 ethoxy sulfates, secondary alky 1 sulfates and mixtures thereof, with a hydrotrope selected from the group consisting of sulf l succinates, xylene sulfonates cumene sulfonates and mixtures thereof Also, the process adds other adjunct detergent ingredients, all of which are thereafter agglomerated in a mixer/densifier to yield detergent agglomerates w hich form the detergent composition For purposes of enhancing biodegradability, the detergent composition does not contain any phosphates

As used herein, the phrase "improved solubility" means that the solubility of the anionic surfactants of the detergent composition is enhanced by at least 5% in the laundenng solution when employed in the manner of this invention, as compared to the solubility of the same anionic surfactants per se, under the same test conditions (i e water temperature and pH, stimng speed and Ume, particle size, water hardness, and the like) As used herein, the term "agglomerates" refers to particles formed by agglomerating particles which typically have a smaller mean particle size than the formed agglomerates All percentages, ratios and proportions used herein are by weight unless otherwise specified All documents including patents and publications cited herein are incorporated herein by reference

In accordance with one aspect of the invention, a process for making a detergent composition in the form of agglomerates is provided herein The process for making a detergent composition compπses the step of adding a paste mixture to a mixer/densifier, wherein the paste mixture includes from about 1% to 50% by weight of a detersive surfactant system compnsing at least about 30% of a sulfated surfactant selected from the group consisting of alkyl sulfates, alkyl ethoxy sulfates. secondary alkyl sulfates and mixtures thereof, and from about 1% to 50% of a hydrotrope selected from the group consisUng of sulfyl succinates, xylene sulfonates cumene sulfonates and mixtures thereof The process also includes the steps of mixing at least about 1% by weight of a detergency builder into the mixer/densifier, and agglomerating the paste mixture and the builder into detergent agglomerates which are substantially free of phosphates The anionic surfactants in the detergent composition have significantly improved dissolution in aqueous laundering solutions, especially those kept at cold temperatures, l e 5°C to 30°C In that regard, the solubility of the sulfated surfactant (AS, AES and/or SAS) is enhanced by at least 5%, preferably 10 to 50% over those same surfactants alone under the same test conditions in aqueous washing solutions at cold temperatures I e 5°C to 10°C Accordingly, it is an object of the present invention to provide a process for making a granular detergent composition which has improved solubility, especially in cold temperature washing solu ons It is also an object of the invention to provide a process for making a detergent

composition which has improved biodegradabilitv These and other objects, features and attendant advantages of the present invention will become apparent to those skilled in the an from a reading of the following detailed descnption of the preferred embodiment and the appended claims DETAILED DESCRIPTION OF THE PREFERRED EMBODIMENT The invention is directed to a process for making a granular detergent composition having improved solubility in cold temperature laundering solutions A multitude of consumers around the world launder soiled clothes in conventional washing machines unique to their particular geographic location Typically, these conventional washing machines launder the soiled clothes in water supplied at relatively cold temperatures, for example in range of 5°C to 30°C, and at high hardness concentrations, e g 7 grains/gallon (rich with Ca and Mg ions) Most of the modern day consumers also use compact or condensed laundry detergents to accomplish their laundenng needs Under the aforementioned conditions, solubility of cuπent detergents in aqueous laundenng solutions has been a problem This problem is especially exacerbated when the detergent composition has high levels of alkyl sulfates, alky 1 ethoxy sulfate and/or secondary alkyl sulfates which are not particularly amenable to dissolution in cold aqueous laundenng solutions Such surfactants are particularly useful in modern laundry detergents since they minimize or eliminate the need for linear alkylbenzene sulfate surfactants hich generally have poor biodegradability It has been found that the solubility of a high-content alkyl sulfate, alkyl ethoxy sulfate and/or secondary alkyl sulfate ("sulfated" surfactant system) detergent composition can be increased by incorporating a hydrotrope selected from the group consisting of sulfyl succinates. xylene sulfonates, cumene sulfonates and mixtures thereof

The Process T e process of the invention initially involves adding a paste mixture to a mixer/densifier Preferably, the paste mixture includes from about 1% to about 50% by weight of a detersive surfactant system compnsing at least about 30%, preferably from about 35% to about 90%, by weight of the surfactant system, of a sulfated surfactant as described previously Additionally, the paste mixture includes from about 1% to 50%, preferably from about 15% to about 40%, by weight of a hydrotrope selected from the group consisting of sulfyl succinates, xylene sulfonates, cumene sulfonates and mixtures thereof The objective is to combine the surfactants and liquid needed in the compositions into a common mix in order to aid in surfactant solubilization and agglomeration In this step, the surfactants, hydrotrope and other optional liquid components are mixed together in a πuxer/denstfier such as a Lodige CB, Lodige KM, twin screw extruder or Schugi Mixer

The next steps of the process entails mixing at least about 1%. preferably from about 10% to about 40%, by weight of a detergency builder into the mixer/densifier. and agglomerating the paste mixture and the builder into detergent agglomerates The purpose of the agglomeration step is to transform the base formula ingredients into fiowable detergent agglomerates having a mean particle size range of from about 800 microns to about 1600 microns and a density of 650 g/1 or

--)-

higher In the process, powders (including materials such as zeolite citrate citπc acid builder layered silicate builder (as SKS-6), sodium carbonate and optionally ethvlenediaminedisuccinate magnesium sulfate and optical bπghtener) are charged into the mixer and the mixing is continued at, for example, about 1500 rpm to about 3000 rpm for a penod from about 1 minute to about 10 minutes at ambient temperature Of course, the operating parameters will depend upon the particular mixer/densifier used in the present process Preferably, the mixer/densifier is operated to obtain course, cπsp, free flowing agglomerates (average particle size 800-1600 microns) with a density of at least 650 g/1 In a prefened embodiment, the process does not involve the addition of phosphates so as to improve the biodegradability of the resulting detergent composition Optionally, the present process may include several additional steps such as reducing the agglomerates' stickiness by removing/drying moisture to aid in particle size reduction to the target particle size (in the mean particle size range from about 800 to about 1600 microns, as measured by sieve analysis) In this optional step, the wet agglomerates are charged into a fluidized bed at an air stream temperature of, for example, from about 41°C to about 60°C and dned to a final moisture content of the particles from about 4% to about 10%

Another optional step of the present proce_o is to admix mateπals which coat the agglomerates, reduce the caking/lumping tendency of the particles and help maintain acceptable flowability In this regard, a mateπals such as Zeolite A (median particle size 2-5 μm) is added dunng agglomeration or pπor thereto into one of the input streams into the mi er/densifier Another optional step is to add a flow aid dunng or after the agglomeration step ti insure the production of cπsp free flowing detergent agglomerates For example, 0 1% to 2% of a precipitated silica (average particle size 1-3 microns) could be used as the flow aid

It has been found that such a detergent composition containing agglomerates having the aforementioned surfactant system and hydrotrope surpπsingly has significantly improved solubility in cold temperature (5°C to 30°C) washing solutions as well as under high water hardness conditions The "improved solubility" achieved by the detergent composition is concerned with enhanced solubility of the anionic surfactants contained in the surfactant system, i e AS, AES SAS or LAS if used Preferably, the improvement represents at least a 5% increase in solubility of these amonics in the wash solution over the solubility of the same surfactants if they were dissolved alone or without being contained in a detergent composition as defined herein More preferably, the solubility improvement is from about 10% to about 50% As those skilled in the art will appreciate any con. - iπson of anionic surfactant solubility should be completed under the same laundenng conditions, e g water temperature, hardness and pH, stimng speed and time, and particle size Typical anionic surfactant solubility improvements are set forth in the Examples hereinafter Those skilled in the art should also appreciate the numerous ways in which the amount of the surfactant system in the washing solution can be deteπnmed For example, in the so-called "catS03" titration technique, samples of the aqueous laundering solution containing the detergent

composition can be taken after one minute and filtered with 0 45 mm nv lon filter HPLC, after which the filtered soluuon can be titrated with a catioiuc titrant hich can be commercially purchased e g from Sigma Chemical Company under the trade name Hvamine in the presence of anionic dves From the foregoing, the amount of anionic surfactant which was dissolv ed in the washing solution can be determined

Surfactant System The surfactant system in the detergent composition must include a sulfated surfactant selected from the group consisting of alkyl sulfates, alkyl ethoxy sulfates, secondary alkyl sulfates, and mixtures thereof As mentioned previously, the anionic surfactants in the surfactant system of the invention, l e AS, AES, and/or SAS, have improved solubility and more particularly, on the order of 5% or higher Optionally, the surfactant system may contain one or more of additional surfactants, nonhmiting examples of which are provided hereinafter

The surfactant system preferably includes conventional pπmary alkyl sulfate surfactants have the general formula ROS0 ₃ ^" M ⁺ wherein R is typically a linear Cιø-C ₂ o hydrocarbyl group and M is a water-solubilizmg cation Branched-chain pnmary alkyl sulfate surfactants (1 e , branched-cham "PAS") having 10-20 carbon atoms can also be used herein, see, for example, European Patent Application 439.316, Smith et al, filed 21 01 91, the disclosure of which is incorporated herein by reference (Included in the term "alkyl" is the alkyl portion of acyl groups) Included in the surfactant system are the C JO _' IS alkyl alkoxy sulfates ("AE _X S", especially EO 1-7 ethoxy sulfates)

Conventional secondary alkyl sulfate surfactants can also be used herein and include those mateπals which have the sulfate moiety distπbuted randomly along the hydrocarbyl "backbone" of the molecule Such mateπals may be depicted by the structure CH ₃ (CH2) _n (CHOSθ3-M ⁺ )(CH ₂ ) _m CH3 wherein m and n are integers of 2 or greater and the sum of m + n is typically about 9 to 17, and M is a water-solubilizing cation

More preferably, a selected secondary (2.3) alkyl sulfate surfactant is used herein which compπses structures of formulas A and B (A) CH ₃ (CH ₂ ) _x (CHOS0 ₃ -M ⁺ ) CH ₃ and

(B) CH ₃ (CH ₂ ) _y (CHOSθ3-M ⁺ )CH ₂ CH ₃ for the 2-sulfate and 3-sulfate, respectively Mixtures of the 2- and 3-sulfate can be used herein In formulas A and B, x and (y+1) are, respectively, integers of at least about 6. and can range from about 7 to about 20, preferably about 10 to about 16 M is a cation, such as an alkali metal, ammomum, alkanolammonium, alkaline earth metal, or the like Sodium is typical for use as M to prepare the water-soluble (2,3) alkyl sulfates. but ethanolammonium. diethanolammomum. tnethanolammonium, potassium, ammonium, and the like, can also be used It is prefened that the

secondary (2,3) alkvl sulfates be substantially free (I e contain less than about 20%, more preferably less than about 10%. most preferably less than about 5%) of such random secondary alkyl sulfates

The preparation of the secondary (2,3) alkyl sulfates of the tvpe useful herein can be earned out by the addition of H S04 to olefins A typical synthesis using α-olefins and sulfuric acid is disclosed in U S Patent 3,234.258, Morns, or in U S Patent 5.075,041 Lutz granted December 24 1991, both of which are incorporated herein by reference The synthesis conducted in solvents which afford the secondary (2,3) alkyl sulfates on cooling, yields products which, when puπfied to remove the unreacted mateπals, randomly sulfated mateπals. unsulfated by-products such as C J _Q and higher alcohols, secondary olefin sulfonates, and the like, are typically 90+% pure mixtures of 2- and 3-sulfated mateπals (up to 10% sodium sulfate is typically present) and are white, non-tacky, apparently crystalline, solids Some 2,3-dιsulfates may also be present but generally compπse no more than 5% of the mixture of secondary (2,3) alkyl mono-sulfates Such mateπals are available as under the name "DAN", e g DAN 200" from Shell Oil Company If increased solubility of the "crystalline" secondary (2,3) alk l sulfate surfactants is desired, the formulator may wish to employ mixtures of such surfactants having a mixture of alkyl chain lengths Thus, a mixture of C^-C _j alkyl chains will provide an increase in solubility over a secondary (2,3) alkyl sulfate wherein the alkyl chain is, say, entirely C _| g The solubility of the secondary (2,3) alkyl sulfates can also be enhanced by the addition thereto of other surfactants such as the mateπal which decreases the crystallinity of the secondary (2,3) alkyl sulfates Such crystallinity-interrupting mateπals are typically effective at levels of 20% or less of the secondary (2,3) alkyl sulfate

Hvdrotrope The granular detergent composition produced by the process of the present invention preferably includes a hydrotrope such a those commonly used in liquid detergents It has been found that the inclusion of a hydrotrope into the agglomerated detergent composition descπbed herein surpπsingly aides in solubilization of detergent agglomerates which are nch in sulfated surfactants (i.e > 30% of the surfactant system) The hydrotrope regardless of form (I e solid, liquid or paste) is mixed with the surfactant paste pπor to, or dunng the agglomeration step Those failed in the art will appreciate the wide variety of hydrotropes useful for the instant detergent composition As mentioned previously, however, the hydrotrope used herein is preferablv selected from the group consisting of sulfyl succinates. xylene sulfonates, cumene sulfonates and mixtures thereof Most prefened are the sodium salts of the aforementioned prefened hydrotropes Other suitable hydrotropes include napthelene sulfonates. benzoates. salicylates, gallates, hydroxy naphthoates, picolinates These and other suitable hydrotropes for use herein are descπbed in known texts such as Mitijevic, "Surface and Colloid Science" Plenum Press, vol 15 ( 1993). the disclosure of which is incorporated herein by reference

Builder The detergent composition produced bv the process of the invention also includes a detergency builder mateπal to assist in controlling mineral hardness Inorganic as well as organic builders can be used Builders are typically used in fabπc laundering compositions to assist in the removal of paniculate soils Inorganic detergent builders include, but are not limited to, the alkali metal, ammonium and alkanolammonium salts of phvtic acid, silicates, carbonates (including bicarbonates and sesquicarbonates), sulphates, and aluminosilicates

Examples of silicate builders are the alkali metal silicates, particularly those having a Sι0 ₂ Na ₂ 0 rauo in the range 1 6 1 to 3 2 1 and layered silicates, such as the layered sodium silicates descπbed in U S Patent 4,664.839, issued May 12. 1987 to H P Rieck NaSKS-6 is the trademark for a crystalline layered silicate marketed by Hoechst (commonly abbreviated herein as "SKS-6") Unlike zeolite builders, the Na SKS-6 silicate builder does not contain aluminum NaSKS-6 has the delta-Na ₂ Sιθ5 morphology form of layered silicate It can be prepared by methods such as those descπbed in German DE-A-3.417,649 and DE-A-3,742.043 SKS-6 is a highly prefened layered silicate for use herein, but other such layered silicates, such as those having the general formula NaMSι _x 0 _x +ι yH ₂ 0 wherein M is sodium or hydrogen, x is a number from 1 9 to 4, preferably 2, and y is a number from 0 to 20, preferably 0 can be used herein Vaπous other layered silicates from Hoechst include NaSKS-5, NaSKS-7 and NaSKS-11, as the alpha, beta and gamma forms As noted above, the delta-Na ₂ Sιθ5 (NaSKS-6 form) is most prefened for use herein Other silicates may also be useful such as for example magnesium silicate, which can serve as a cnsping agent in granular formulations, as a stabilizing agent for oxygen bleaches, and as a component of suds control systems

Examples of carbonate builders are the alkaline earth and alkali metal carbonates as disclosed in German Patent Application No 2,321,001 published on November 15, 1973 Aluminosihcate builders are useful in the present invention Aluminosilicate builders are of great importance in most cunently marketed heavy duty granular detergent compositions, and can also be a significant builder ingredient in liquid detergent formulations Aluminosilicate builders include those having the empiπcal formula wherein z and y are integers of at least 6, the molar ratio of z to y is in the range from 1 0 to about 0 5, and x is an integer from about 15 to about 264

Useful aluminosilicate ion exchange materials are commercially available These aluminosilicates can be crystalline or amorphous in structure and can be naturally-occurnng aluminosilicates or synthetically denved A method for producing aluminosilicate ion exchange mateπals is disclosed in U S Patent 3,985.669, Krummel. et al, issued October 12, 1976 Preferred synthetic crystalline aluminosilicate ion exchange materials useful herein are available under the

designations Zeolite A. Zeolite P (B) Zeolite MAP and Zeolite X In an especially preferred embodiment, the crystalline aluminosilicate ion exchange material has the formula

Na ₁₂ [(A10 ₂ ) ₁ 2(Sι0 ₂ ) ₁₂ ] xH ₂ 0 wherein x is from about 20 to about 30, especially about 27 This material is known as Zeolite A Dehydrated zeolites (x = 0 - 10) may also be used herein Preferably, the aluminosilicate has a particle size of about 0 1-10 microns in diameter

Organic detergent builders suitable for the purposes of the present invention include but are not restπcted u wide vaπety of polycarboxylate compounds As used herein, "poly¬ carboxylate" refers to compounds having a plurality of carboxylate groups preferably at least 3 carboxylates Polycarboxylate builder can generally be added to the composition in acid form, but can also be added in the form of a neutralized salt When utilized in salt form, alkali metals, such as sodium, potassium, and lithium, or alkanolammonium salts are preferred

Included among the polycarboxylate builders are a vaπety of categories of useful mateπals One important category of polycarboxylate builders encompasses the ether pol carboxvlates, including oxydisuccinate, as disclosed in Berg, U S Patent 3,128,287, issued Apπl 7, 1964, and Lamberti et al, U S Patent 3,635,830, issued January 18, 1972 See also "TMS DS" builders of U S Patent 4.663,071, issued to Bush et al, on May 5, 1987 Suitable ether polycarboxvlates also include cyclic compounds, particularly a cyclic compounds, such as those descπbed in U S Patents 3,923,679, 3,835,163, 4,158,635, 4, 120,874 and 4, 102,903 Other useful detergency builders include the ether hydroxypolycarboxylates, copolymers of maleic anhydnde with ethylene or vinyl methyl ether, 1, 3, 5-tπhydroxy benzene-2, 4, 6- tπsulphonic acid, and carboxymethyloxysuccinic acid, the vaπous alkali metal, ammonium and substituted ammonium salts of polyacetic acids such as ethylenediamine tetraacetic acid and nitnlotπacetic acid, as well as polycarboxvlates such as mellitic acid, succimc acid, oxvdisucci c acid, polymaleic acid, benzene 1,3,5-tπcarboxylιc acid, carboxymethyloxysuccinic acid, and soluble salts thereof

Citrate builders, e g , citnc acid and soluble salts thereof (particularly sodium salt), are polycarboxylate builders of particular importance for heavy duty liquid detergent formulations due to their availability from renewable resources and their biodegradabi ty Citrates can also be used. however, in granular compositions, especially in combination with zeolite and/or layered silicate builders Oxydisuccinates are also especially useful in such compositions and combinations

Also suitable in the detergent compositions of the present invention are the 3 3-dιcarboxv- 4-oxa-l,6-hexanedιoates and the related compounds disclosed in U S Patent 4.566,984, Bush, issued January 28, 1986 Useful succimc acid builders include the C5-C ₂ Q alkyl and alkenyl succimc acids and salts thereof A particularly prefened compound of this type is dodecenylsuccinic acid Specific examples of succinate builders include laurylsuccinate, mynstylsuccinate palmitylsuccinate, 2-dodecenylsuccιnate (prefened), 2-pentadecenylsuccιnate. and the like

Laurylsuccinates are the preferred builders of this group and are descπbed in European Patent Application 86200690 5/0 200,263, published Nov ember 5, 1986 Other suitable polycarboxv lates are disclosed in U S Patent 4 144,226 Crutchfield et al issued March 13 1979 and in U S Patent 3,308,067, Diehl, issued March 7, 1967 See also Diehl U S Patent 3.723,322 Fatty acids, e g , Cι ₂ -Cιg monocarbox lic acids, can also be incorporated into the compositions alone, or in combination with the aforesaid builders, especially citrate and/or the succmate builders, to provide additional builder activity Such use of fattv acids will generally result in a diminution of sudsing, which should be taken into account by the formulator

Adiunct Surfactants One or more adjunct surfactants may be included generally at a level of from about 1% to about 50% of the surfactant system descπbed herein Nonlimiting examples of surfactants useful in conjunction with the surfactants descπbed herein are the C _jQ -C _j alkyl alkoxy carboxylates (especially the EO 1-5 ethoxycarboxylates), the C _j o-ig glycerol ethers the C _j ø-C ig alkyl polyglycosides and their conesponding sulfated polyglycosides, and C ₁₂ -C _j alpha-sulfonated fatty acid esters If desired, the conventional nomonic and amphotenc surfactants such as the C _{j 2} -C _j g alkyl ethoxy lates ("AE") including the so-called nanovv peaked alkyl ethoxy lates and C^-C^ alkyl phenol alkoxylates (especially ethoxylates and mixed ethoxv/propoxy), C ι ₂ -C _[ betaines and sulfobetaines ("sultaines"), can also be included in the overall compositions The Ciø-C _j g N-alkyl polyhydroxy fatty acid amides can also be used Typical examples include the C _{j 2} -Cιg N- methylglucamides See WO 9,206, 154 The N-propyl through N-hexyl C ι ₂ -C ιg glucamides can be used for low sudsing Cιo-C ₂ o conventional soaps may also be used If high sudsing is desired, the branched-cham Cio- _j g soaps may be used

Also included in the surfactant system is the conventional C _{j j} -C _j alkyl benzene sulfonates (also referenced herein as "LAS) While the biodegradability of the so-called "LAS" surfactants have been the subject of some concern, the surfactant system herein may include an optimum level, from about 0 1% to about 15% and more preferably from about 3% to about 8% by weight, for improving the overall solubility of the detergent composition without substantially decreasing the overall biodegradability of the present detergent composition Alternatively, the level of LAS may be included as from about 1% to about 40%, more preferably from about 10% to about 25%, by weight of the surfactant system in the detergent composition

The surfactant system may also include an amine oxide surfactant Nonlimiting examples include C _I Q-18 amme oxides, secondary amine oxides such as dimethyl amine oxide, and tertiar ^y arrune oxides having the general formula RR'R"NO in w ich R is a primary alkyl group containing 8 to 24 carbon atoms, R' is methyl, ethyl, or 2-hydroxyethyl, and R" is independently selected from methyl, ethyl, 2-hydroxyethly and pnmary alkyl groups containing 8 to 24 carbon atoms

Additionally, the tertiary amine oxide surfactant may be in hydrated form and have the general formula RR'R"NO nH ₂ 0 wherein R, R' and R" are the same as above and n is 1 or 2 Examples of

other tertiary amines suitable for use herein include those containing one or two short-chain groups independently selected from methyl, ethyl, and 2-hydroxvethyl groups with the remaining valences of the arruno nitrogen being satisfied with long-chain groups independently selected from pπmarv alkyl groups containing 8-24 carbons, e g , octyl, dec l dodecyl, tetradec l hexadec l, octadecyl, eicosyl, docosyl, and tetracosyl groups The pπmarv alk l groups may be branched-chain groups, but the prefened amines are those in which at least most of the pπmary alkyl groups have a straight chain

Exemplary of these tert-amines are N-octyldimethylamine. N N-didecvlmethvlamine N- decyl-N-dodecylethylamine, N-dodecyldimethylamine, N-tetradecyldimethylamine, N-tetradecyl-N- ethylmethylamine, N-tetradecyl-N-ethyl-2-hydroxyethvlamιne. N N-dι-tetradecyl-2- hydroxyethylamine, N-hexadecyldimethylamine, N-he\adecyldι-2- hdroxyethylamine N- octadecyldimethylamine, N,N-dιeιcosylethylamιne, N-docosyl-N-2-hydrox ethylmethylamine, N- tetracosyldimethylamine, etc

Additional amine oxide surfactants and methods of making the same, all of which are suitable for use herein, are disclosed by Borland et al, U S Patent No 5,071,594 and Tosaka et al, U S Patent No 5,096,621, incorporated herein by reference

Mixtures of anionic and no onic surfactants are especially useful Other conventional useful surfactants are listed in standard texts

Detergent Adiunct Ingredients The detergent composition produced by the process of the invention can also include any number of additional ingredients These include detergency builders, bleaches, bleach activators, suds boosters or suds suppressers, anti-tarnish and anticonosion agents, soil suspending agents, soil release agents, germicides, pH adjusting agents, non-builder alkalinity sources, chelating agents, smectite clays, enzymes, enzyme-stabilizing agents and perfumes See U S Patent 3,936,537, issued February 3. 1976 to Baskerville, Jr et al , incorporated herein by reference Also, fabric conditioning agents may be included as an adjunct mateπal such as those described in U S Patent 4,861,502, issued August 29 1989 to Caswell, incorporated herein by reference

Bleaching agents and activators are descπbed in U S Patent 4,412,934, Chung et al , issued November 1, 1983, and in U S Patent 4,483,781, Hartman, issued November 20, 1984, both of which are incorporated herein by reference Chelating agents are also descπbed in U S Patent 4.663,071 Bush et al , from Column 17, line 54 through Column 18, line 68, incorporated herein by reference Suds modifiers are also optional ingredients and are described in U S Patents 3,933,672, issued January 20, 1976 to Bartoletta et al , and 4, 136,045. issued January 23, 1979 to Gault et al , both incorporated here.n by reference Suitable smectite clays for use herein are descπbed in U S Patent 4,762,645, Tucker et al, issued August 9, 1988, Column 6, line 3 through Column 7, line 24, incorporated herein by reference Suitable additional detergency builders for use herein are enumerated in the Baskerville patent Column

13, line 54 through Column 16 line 16 and in U S Patent 4 663 071 Bush et al issued May 5 1987 both incorporated herein by reference

Enzvmes can be included in the formulations herein for a v ide variety of fabπc laundenng purposes including removal of protein-based, carbohydrate-based or tnglvceπde-based stains, for example, and for the prevention of refugee dye transfer and for fabπc restoration The enzvmes to be incorporated include proteases, amylases, lipases, cellulases and peroxidases as well as mixtures thereof Other types of enzymes may also be included They may be of any suitable oπgin, such as vegetable, animal, bacteπal, fungal and yeast oπgin However, their choice is governed by several factors such as pH-activity and/or stability optima thermostability, stability versus active detergents builders and so on In this respect bacteπal or fungal enzymes are preferred such as bactenal amylases and proteases, and fungal cellulases

Suitable examples of proteases are the subtilisins which are obtained from particular strains of B subtilts and B licheniforms Another suitable protease is obtained from a strain of Bacillus, having maximum activity throughout the pH range of 8-12, developed and sold by Novo Industπes A/S under the registered trade name ESPERASE The preparation of this enzyme and analogous enzymes is descnbed in Bπtish Patent Specification No 1,243,784 of Novo Proteolvtic enzymes suitable for removing protein-based stains that are commercially available include those sold under the trade names ALCALASE and SAV1NASE by Novo Industπes A S (Denmark) and MAXATASE by International Bio-Synthetics, Inc (The Netherlands) Other proteases include Protease A (see European Patent Application 130,756, published January 9, 1985) and Protease B (see European Patent Application Seπal No 87303761 8, filed Apπl 28, 1987, and European Patent Application 130,756, Bott et al, published January 9, 1985)

Amylases include, for example, α-amylases descπbed in Bπtish Patent Specification No 1,296,839 (Novo), RAPIDASE, International Bio-Synthetics. Inc and TERMAMYL Novo Industπes

The cellulase usable in the present invention include both bacterial or fungal cellulase Preferably, they will have a pH optimum of between 5 and 9 5 Suitable cellulases are disclosed in U.S Patent 4,435,307, Barbesgoard et al, issued March 6, 1984, which discloses fungal cellulase produced from Humicola insolens and Humicola strain DSM1800 or a cellulase 212-producιng fungus belonging to the genus Aeromonas, and cellulase extracted from the hepatopancreas of a manne mollusk (Dolabella Auncula Solander) suitable cellulases are also disclosed in GB-A- 2 075 028, GB-A-2 095 275 and DE-OS-2 247 832

Suitable lipase enzymes for detergent usage include those produced bv microorganisms of the Pseudomonas group, such as Pseudomonas stutzeπ ATCC 19 154, as disclosed in Bπtish Patent 1,372,034 See also lipases in Japanese Patent Application 53,20487 laid open to public inspection on February 24, 1978 This lipase is available from Atnano Pharmaceutical Co Ltd , Nagoya, Japan, under the trade name Lipase P "Amano," hereinafter refened to as "Amano-P " Other

commercial lipases include Amano-CES lipases ex Chromobacter v iscosum e g Chromobacter viscosum var lipolyticum NRRLB 3673 commercially available from Toy o Jozo Co Tagata Japan, and further Chromobacter viscosum lipases from U S Biochemical Corp U S A and Disoynth Co , The Netherlands, and lipases ex Pseudomonas gladioli The LIPOLASE enzyme deπved from Humicola lanuginosa and commercially available from Novo (see also EPO 341 947) is a prefened lipase for use herein

Peroxidase enzymes are used in combination with oxygen sources, e g , percarbonate, perborate, persulfate, hydrogen peroxide, etc Thev are used for "solution bleaching," i e to prevent transfer of dyes or pigments removed from substrates dunng wash operations to other substrates in the wash solution Peroxidase enzymes are known in the an and include for example horseradish peroxidase, ligninase, and haloperoxidase such as chloro- and bromo-peroxidase Peroxidase- containing detergent compositions are disclosed for example in PCT International Application WO 89/099813, published October 19, 1989, by 0 Kirk, assigned to Novo Industπes A/S

A wide range of enzyme materials and means for their incorporation into synthetic detergent compositions are also disclosed in U S Patent 3,553,139, issued January 5, 1971 to

McCarty et al Enzymes are further disclosed m U S Patent 4,101 457. Place et al, issued July 18, 1978, and in U S Patent 4,507,219. Hughes issued March 26 1985 both Enzv e mateπals useful for liquid detergent formulations, and their incorporation into such formulations are disclosed in U S Patent 4,261,868, Hora et al, issued Apπl 14, 1981 Enzymes for use in detergents can be stabilized by vanous techniques Enzyme stabilization techniques are disclosed and exemplified in U S Patent 3,600,319, issued August 17, 1971 to Gedge, et al, and European Patent Application Publication No 0 199 405, Application No 86200586 5, published October 29, 1986, Venegas Enzyme stabilization systems are also descπbed, for example, in U S Patent 3,519,570 Additionally, dye transfer inhibiting agents may also be included, for example, polyvmylpyrrolidone, polyamine N-oxide, copolymers of N-vinylpyrrolidone and N-vtnvlimidazole are a suitable dye transfer inhibiting polymers for use in the present detergent composition The level of such addiUonal dye transfer inhibiting agents may vary, but typically will be from about 0 01% to about 10% by weight of the detergent composition

In order to make the present invention more readily understood, reference is made to the following examples, which are intended to be illustrative only and not intended to be limiting in scope

EXAMPLE I Several detergent compositions (A-C) are made in accordance with the process described above Compositions A and B are within the scope of the invention and composition C is outside of the invention and is presented for purposes of companson as described in Example II hereinafter The relative proportions of compositions A-C in agglomerate form, are listed in Table I below

A B C

Component Surfactants % (wt.) % (wt.) % (w t.) -14-I5 pnmary alkyl sulfate 18 8 18 8 19 2 ^c 12" ^c 15 ^alk y' ^et hoxy (1-3) sulfate 10 6 10 6 10 8

Sulfyl succinate 2 0

Xylene sulfonate 2 0

Builders

Zeolite 4A 39 2 39 2 40 0

Carbonate (Na) 15 8 15 8 16 1

Additives

Misc. (water, perfume and minors) 13 6 13 6 13 9

00 0 100 0 100 0

EXAMPLE II

This Example illustrates the surpπsingly improved solubility achieved by the detergent composition made according to the process of the invention. Specifically, standard dosages of compositions A-C (1170 ppm) are dissolved in an aqueous laundenng solution having a water temperature of 10°C and a water hardness of 7 grains/gallon (Ca:Mg ratio of 3.1). The laundenng solution is continuously agitated at a rate of 75 rpm and samples of the wash solution were taken at various ume intervals as shown in Table I below. For purposes of illustrating the improved solubility of the detergent composition according to the invention, the amount of surfactant in the laundenng solution is determined by conducting the well known "catS0 ₃ " turation technique on the samples taken from individual wash solutions containing one of the compositions A-C In particular, the amount of anionic surfactant in the laundering solution is determined by filteπng the samples through 0.45 nylon filter paper to remove the msolubles and thereafter, titrating the filtered solution to which anionic dyes (dimidium bromide) have been added with a cationic titrant such as Hyamine™ commercially available from Sigma Chemical Company Accordingly, the relative amount of anionic surfactant dissolved in the wash solution can be determined This technique is well known and others may be used if desired The results are shown in Table II below

TABLE π

(% total of anionic dissolved)

Time (Minutes) A B C

0 0% 0% 0%

1 22% 37% 22%

3 29% 45% 34%

10 52% 58% 34%

From the results in Table II. it is quite clear that compositions A and B which are within the scope of the invention suφπsingly have improved solubility over composition C which is outside the scope of the invention.

Having thus described the invention in detail, it will be obvious to those skilled in the art that vanous changes may be made without departing from the scope of the invention and the invention is not to be considered limited to what is described in the specification