EP0000225A1

EP0000225A1 - Solid detergent composition for improved greasy soil removal

Info

Publication number: EP0000225A1
Application number: EP78200050A
Authority: EP
Inventors: Rory James Maxwell Smith; Allan Campbell Mcritchie; Lionel Breton
Original assignee: Procter and Gamble Co
Current assignee: Procter and Gamble Co
Priority date: 1977-06-29
Filing date: 1978-06-20
Publication date: 1979-01-10
Also published as: GR63770B; DE2857163C2; NL7815015A; FR2423537A1; SE446460B; FR2423537B1; MX147454A; AU3758778A; CH643881A5; AU525063B2; IT1097286B; SE7907257L; AT400244B; ATA469178A; IT7825093A0; DE2857163A1; JPS5439417A; BR7804163A

Abstract

Built laundry detergent compositions containing specific mixtures of selected anionic, nonionic and water-soluble cationic surfactants. The compositions are especially effective in removing greasy soil from fabrics.

Description

This invention relates to detergent compositions
improved greasy soil removal capabilities. More specifically the detergent compositions of this invention provide
good detergency performance on greasy and oily soils having a marked particulate soil content.
Cationic surfactants have been frequently incorporated into detergent compositions of various types. However, the Inclusion of such cationic surfactants is generally for the purpose of providing some adjunct fabric care benefit, and not for the purpose of cleaning. For example, certain catronic surfactants have been included in detergent
compositions for the purpose of yielding a germicidal or sanitization benefit to washed surfaces, as is disclosed in U.S. Patent 2,742,434, Kopp, issued April 17, 1956; U.S. Patent 3,539,520, Cantor et al, issued November 10, 1970; and U.S. Patent 3,965,026, Lancz, issued June 22, 1976. Other cationic surfactants, such as ditallowdimethylammonium chloride, have been included in detergent compositions for the purpose of yielding a fabric-softening benefit, as disclosed in U.S. Patent 3,607,763, Salmon et al, issued September 21, 1971; and U.S. Patent 3,644,203, Lamberti et al, issued February 22, 1972. Such components are also disclosed as being included in detergent compositions for the purpose of controlling static, as well as softening laundered fabrics, in U.S. Patent 3,951,879, Wixon, issued April 20, 1976; and U.S. Patent 3,959,157, Inamorato, issued May 25, 1976.
Compositions comprising mixtures of anionic, cationic and nonionic surfactants are also known in the art. Thus, compositions conferring enhanced antistatic character to textiles washed therewith are described in B.P. 873,214 while compositions having enhanced germidical and detergency performance are disclosed in B.P. 641,297.
Surprisingly, it has now been found, however, that built detergent compositions comprising water-soluble or dispersible mixtures of specific anionic, cationic and nonionic surfactants in critical relative amounts provide unexpectedly improved cleaning performance on greasy and oily soils, even where these have a high content of particulate matter. Moreover, this excellent performance is observed at both high and low wash temperatures and over a range of realistic soil types and wash conditions. Furthermore, the enhanced greasy stain removal performance is achieved without detriment to detergency performance on conventional soil and stain types and most surprisingly,
detriment to the soil suspending or fabric whitening characteristics of the compositions.

Summary of the Invention

According to the present invention, there is provided a solid particulate detergent composition comprising

(a) from 2% to 60% of a surfactant system consisting essentially of a water-soluble or water-dispersible combination of anionic, alkoxylated nonionic and water-soluble quaternary ammonium cationic surfactants, wherein the anionic:cationic surfactant weight ratio is no more than 5:1 and the nonionic:cationic surfactant weight ratio is in the range from 100:1 to 2:3, and wherein the surfactant system contains anionic and cationic surfactants in an equivalent ratio of at least 1:1, and
(b) at least 10% of a detergency builder.

Detergent compositions of the present invention contain as an essential ingredient a three-component active system comprising anionic, alkoxylated nonionic and water-soluble cationic surfactants. This active system comprises from about 2% to about 60% by weight of the compositions. In granular laundry detergent applications, the active system is generally in the range from about 4% to about 30%, more preferably from about 6% to about 15% by weight of the compositions.
The compositions of the present invention are pref- ably formulated to have a pH of at least about 6 in the laundry solution at conventional usage concentrations (about 1% by weight) in order to optimize cleaning performance. More preferably, they arc alkaline in nature when placed in the laundry solution and have a pH greater than about 7, especially greater than about 8. At the higher pH values, the surface activity of the compositions of the invention is enhanced and, in certain instances, is quite markedly enhanced.
In preferred systems, the anionic and cationic surfactants have a combined total of no more than 34 carbon atoms counted in hydrophobic groups having at least 4 consecutive carbon atoms (eg. alkyl, alkaryl, aryl, alkaryl, aralkyl groups etc.). In more preferred systems the number of such hydrophobic group carbon atoms totals from about 18 to 33, especially from about 26 to 32, with the anionic surfactant providing at least 12 of the carbon atoms. These hydrophobicity limitations have been found to optimize the interaction of the ternary active system with greasy and oily stains on fabrics and to correspond to compositions of maximum grease detergency effectiveness.
An essential feature of the present compositions is that the surfactant system must be substantially neutral in surfactant anions and cations or else have an ionic excess of surfactant anions over surfactant cations. This is important not only with regard to optimizing grease removal, but also for ensuring good suspension of soil in the detergent wash liquor (ie. for preventing soil redeposition) and also for ensuring that water-insoluble anionic effect agents such as anionic florescers retain their effectiveness in composition. It is, of course, well known, that anionic fluorescers are quenched or inhibited in effectiveness in the presence cf cationic surfactants. Surprisingly, the grease and oil detergency benefits of the present invention are secured without suppression of fluorescer activity. It is accordingly highly important that the overall anionic:cationic surfactant equivalent ratio in the present compositions is, within manufacturing error, at least 1:1.
At typical composition levels, the manufacturing
in the anionic and cationic surfactant components
5% by weight for each component.
Subjet to the above conditions be weight ratio of anionic:cationic surfactant can vary in the range from about 5:1 to about 1:3, especially From about 2:1 to about 1:2, the weight ratio of nonionic:cationic from about 300:1 to about 2:3, especially from about 20:1 to about.1:1, and the weight ratio of anionic: nonionic from about 7:1 to about 1:20, especially from. about 2:1 to about 1:10. In terms of surfactant levels, the surfactant system preferably comprises at least about 5% by weight of the water-soluble cationic surfactant and at least about 60% by weight in total of the anionic and nonionic surfactants. In one preferred embodiment, the surfactant system comprises at least 15% by weight of each of the anionic and cationic surfactants and from 15% to 60% by weight of the nonionic surfactant. In another preferred embodiment, the surfactant system comprises at least 5% by weight of each of the anionic and cationic surfactants-and at least 60% by weight of the nonionic surfactant.
As mentioned above, the cationic surfactant component of the composition of the invention is characterised as being water-soluble. By water solubility, we refer in this context to the solubility of cationic surfactant in monomeric form, the limit of solubility being determined by the onset of micellisation and measured in terms of critical micelle concentration (C.M.C.). The cationic surfactant should thus have a C.M.C. for the pure material greater than about 200 p.p.m. and preferably greater than about 500 p.p.m., specified at 30°C and in distilled water. Literature values are taken where possible, especially surface tension or conductimetric values - see Critical Micelle Concentrations of Aqueous Surfactant Systems, P. Mukerjee and K.J. Mysels, NSRDS-NBS 36, (1971).
Another important feature is that the ternary active system itself must be water-dispersible or water-soluble in combination with the remainder of the detergent composition. This implies that, in an equilibrium aqueous mixture of the detergent composition(containing about 1000 p.p.m. of surfactant)the ternary active system exists in one or more liquid, (as opposed to solid) surfactant/ water phases. Expressed in another way, the surfactant
A further essential component of the present compositions is at least 10%, preferably from about 20% to about.70% by weight of a detergency builder, for example, a water-soluble inorganic or organic electrolyte, Suitable electrolytes have an equivalent weight of less than 210, especially less than 100 and Include the common alkaline polyvalent calcium ion sequestering agents. Water-insoluble calcium ion exchange materials can also be used with advantage, however. Surprisingly, it is found that the grease removal performance of the present compositions depends sensitively on the ionic strength and the level of free hardness ions in the detergent liquor and these parameters must be closely controlled for optimum performance. Thus, when the compositions are used in about 1% solution, the builder: surfactant weight ratio is preferably greater than about 1:3, more preferably greater than about 4:1 and especially greater than about 8:1. The weight ratio of calcium ion sequestering or exchange agent:surfactant, on the other hand, is preferably greater than about 1:1 and especially greater than about 3:1, wnile the electrolyte:surfactant weight ratio is preferably greater than about 3:1, especially greater than about 6:1.
Optimum grease and particulate detergency also depends sensitively on the choice of nonionic surfactant and especially desirable from the viewpoint of grease detergency are biodegradable nonionic surfactants having a lower consolute temperature in the range from about 25°C to about 65°C, more preferably from about 30°C to about 50°C. Highly suitable nonionic surfactants of this type have the general formula RO(CH₂CH₂0)_nH wherein R is primary or secondary branched or unbranched C₉_₁₅ alkyl or alkenyl and n (the average degree of ethoxylation) is from 2 to 9, especially from 3 to 8. More hydrophilic nonionic detergents can be employed for providing particulate detergency and anti-redeposition, however, for instance, nonionic detergents of the general formula given above wherein R is primary or secondary,-branched or unbranced C_8-24 alkyl or alkenyl and n is from 10 to 40. Combinations of the two classes of nonionic surfactants

The Caltionic Surfactant
The caltonic surfactant is a water-soluble quaternary ammonium compound having a critical micelle concentration of at least 200 p.p.m. at 30°C In structural terms, the preferred cationic surfactant comprises from 1 to about 4 quaternary ammonium groups of which only one has the general formula:-
wherein each R¹ is a hydrophobic alkyl or alkenyl group optionally substituted or 'nterrupced by phenyl, ether, ester or amide groups totalling from 8 to 20 carbon atoms and which may additionally contain up to 20 ethoxy groups, m is a number from 1 to 3 and no more than one R¹ can have more than 16 carbon atoms when m is 2 and no more than 12 carbon atoms when m is 3, each.R² is an alkyl group containing from one to four carbon atom or a benzyl group with no more than one R² in a molecule being benzyl, and x is from 0 to 3.
A highly preferred group of cationic surfactants of this type have the general formula:

ammonium halide and di-C₁₀ alkyldimethylammonium halide materials.
Where m is equal to 3, the R¹ chains should be less than 9 carbon atoms in length. An example is trioctyl- methyl ammonium chloride. The reason for this chain length restriction, as is also the case with the di-long chain cationics described above, is the relative insolubility of these tri - and di-long chain materials.
Another group of useful cationic compounds are the polyammonium salts of the general formula:
wherein R₃is selected from C₈ to C₂₀ alkyl, alkenyl and alkaryl groups; each R₄ is C₁-C₄ alkyl; n is from 1 to 6; and m is from 1 to 3.
A specific example of a material in this group is:
A further preferred type of cationic component, was the formula:
wherein R^1. is C₁ to C₄ alkyl; R² is C⁵ to C₃₀ straight or branched chain alkyl or alkenyl, alkyl benzene, or
R³ is C₁ to C₂₀ alkyl or alkenyl; a is 0 or 1; n is O or 1; m is from 1 to 5; Z² and Z² are each selected from the group consisting of:
and wherein at least one of said groups is selected from the group consisting of ester, reverse ester, amide and reverse amide; and X is an anion which makes-the compound water-soluble, preferably selected from the group consisting of aride, methyl sulfate, hydroxide, and nitrate preferably chloride, bromide or iodine.
In addition to the advantages of the other cationic surfactants disclosed herein, this particular cationic component is enviromentally desirable, since it is biode-, gradable, both in terms of its long alkyl chain and its
containing segment.
preferred cationic surfactants of this by the choline ester derivatives having the following formula :
as well as those wherein the ester linkage in the above formula is replaced with a reverse ester, amide or reverse
Particularly preferred examples of this type of c sulfactant include caproyl choline ester quat-
halides (R² = C₉ alkyl palmitoyl choline esler quaternary ammonium halides (R² = C₁₅ alkyl) , myristoyl choline ester quaternary ammonium halides (R³ = C₁₃ alkyl), lauroyl chloine ester ammonium halides (R² = C₁₁ alkyl), and capryloyl choline ester quaternary ammonium halides (R² = C ₇ alkyl) .
Additional preferred cationic components of the choline ester variety are given by the structural formulas below, wherein p may be from 0 to 20.
The preferred choline-derivative cationic substances, discussed above, may be prepared by the direct esterification of a fatty acid of the desired chain length with dimethylaminoethanol, in the presence of an acid catalyst. The reaction product is then quaternized with a methyl halide, forming the desired cationic material. The choline-derived cationic materials may also be prepared by the direct esterification of a long chain fatty acid of the desired chain length together with 2-halocthanol, in the presence of an acid catalyst material. The reaction product is then used to quaternize triethanolamine, forming the desired cationic component.
Another type of novel particularly preferred cationic material, has the formula :

and wherein at least one of said groups is selected from the group consisting of ester, reverse ester, amide and reverse amide. X is an anion which will make the compound water-soluble and is selected from the group consisting of halides, methylsulfate, hydroxide and nitrate, particularly chloride, bromide and iodide.
These surfactants, when used in the compositions of the present invention, yield excellent particulate soil, body soil, and grease and oil soil removal. In addition, the detergent compositions control static nd soften the fabrics laundered therewith, and inhibit the transfer of dyes in the washing solution. Further, these novel catienic surfactants are environmentally desirable, since both their long chain alkyl segments and their nitrogen segments are biodegradable.
The preferred choline derivatives, described above, may be prepared by the reaction of a long chain alkyl polyalkoxy (preferably polyethoxy) carboxylate, having an alkyl chain of desired length, with oxalyl chloride, to form the corresponding acid chloride. The naid chloride is then reacted with dimethylaminoethanol to form the appropriate amine ester. which is then quaternized with a methyl halide to form the desired choline ester compound. Another way of preparing these compounds is by the direct esterification of the appropriate long chain ethoxylated carboxylic acid together with 2-haloethanol or dimethyl aminoethanol, in
of heat and an acid
product.
is then quaternized
er used to

The Anionic and Nonionic Surfactant

A typical listing of anionic and nonionic surfactants useful herein appears in U.S.P. 3, 925, 678 incorporated herein by reference, The following list of detergent compounds which can be used in the instant compositions is representative of such materials.
Water-soluble salts of the higher fatty acids, ie. "soaps", are useful as the anionic detergent component of the compositions herein. This class of detergents includes ordinary alkali metal soaps such as the sodium, potassium, ammonium and alkylolammonium salts of higher fatty acids containing from about 8 to about 24 carbon atoms and preferably from about 10 to about 20 carbon atoms. Soaps can be made by direct saponification of fats and soils or by the neutralization of free fatty acids. Particularly useful are the sodium and potassium salts of the mixtures of fatty acids derived from coconut oil and tallow, i.e. sodium or potassium tallow and coconut soap.
A highly preferred class of anionic detergents includes water-soluble salts, particularly the alkali metal, ammonium and alkylolammonium salts, of organic sulfuric reaction products having in their molecular structure an alkyl group containing from about 8 to about 22, especially from about 10 to about 20 carbon atoms and a sulfonic acid or sulfuric acid ester group. (Included in the term "alkyl" is the alkyl portion of acyl groups). Examples of the detergent compositions of the present invention are the sodium and potassium alkyl sulfates, especially those obtained by sulfating the higher alcohols C₈-C₁₈ carbon atoms) produced by reducing the glycerides of tallow or coconut oil; and sodium and potassium alkyl benzene sulfonates, in which the alkyl group contains from about 9 to about 15 carbon atoms, in straight chain or branched chain configuration, e.g. those of the type described in U.S.P. 2,220,099 and 2,477,383. Especially valuable are linear straight chain alkyl benzene sulfonates in which the average of the alkyl group is about 11.8 carbon atoms, abbreviated as C_11.8 LAS.
Λ preferred alkyl ether sulfate surfactant component of the present invention is a mixture of alkyl ether sulfates, said mixture having an
mean) carbon chain length within the range of about 12 to 16 carbon atoms, preferably from about 14 to 15 carbon atoms, and an average (arithmetic mean) degree of "ethoxylation of from about 1 to 4 mols of ethylene oxide.
Other anionic detergent compounds herein include the sodium alkyl glyceryl ether sulfonates, especially those ethers of higher alcohols derived from callow and coconut oil; sodium coconut oil fatty acid moncglyceride sulfonates and sulfates; and sodium or potassium salts of alkyl phenol ethylene oxide ether sulfate containing about 1 to about 10 units of ethylene oxide per molecule and wherein the alkyl groups contain about 8 to about 12 carbon atoms.
Other useful anionic detergent compounds herein include the water-soluble salts of esters of a-sulfonated fatty acids containing from about 6 to 20 carbon atoms in the fatty acid group and from about 1 to 10 carbon atoms in the ester group; water-soluble salts of 2-acyloxy-alkane-1-sulfonic acids containing from about 2 to 9 carbon atoms in the acyl group and from about 9 to about 23 carbon atoms in the alkane moiety: alkyl ether sulfates containing from about 10 to 20 carbon atoms in the alkyl group and from about 1 to 30 moles of ethylene oxide; water-soluble salts of clefin sulfonates containing from about 12 to 24 carbon atoms; water-soluble salts of paraffin sulfonates containing from about 8 to 24, especially 14 to 18 carbon atoms, and β-alkyloxy alkane sulfonates containing from about 1 to 3 carbon atoms in the alkyl group and from about to 20 carbon atoms in the alkane moiety.
Anionic surfactant mixtures can also be employed, for example 5:1 to 1:5 mixtures of an alkyl benzene sulfonate naving from 9 to 15 carbon atoms in the alkyl radical and mixtures thereof, the cation being an alkali metal preferably sodium: and from about 2% to about 15% by weight of an alkyl ethoxy sulfate saving from 10 to 20 carbon atoms in the alkyl radical and from 1 to 30 ethoxy groups and mixtures thereof, having an alkali metal cation, preferably sodium. The nonionic detergent materials can be broadly defined as compounds produced by the condensation of alkylene oxide groups (hydrophilic in nature) with an organic hydrophobic compound, which may be aliphatic or alkyl aromatic in nature. The length of the polyoxyalkylene group which is condensed with any particular hydrophobic group can be readily adjusted to yield a water-soluble compound having the desired degree of balance between hydrophilic and hydrophobic elements.
Examples of suitable nonionic detergents include:

1. The polyethylene oxide condensates of alkyl phenol, eg. the condensation products of alkyl phenols-having an alkyl group containing from 6 to 12 carbon atoms in either a straight chain or branched chain configuration, with ethylene oxide, the said ethylene oxide being present in amounts equal to 1 to 40 moles, preferably from 2 to 9 moles of ethylene oxide per mole of alkyl phenol. The alkyl substitutent in such compounds may be derived, for example, from polymerised propylene, di-isobutylene, octene or nonene. Other examples include dodecylphenol condensed with 12 moles of ethylene oxide per mole of phenol; dinonylphenol condensed with 5 moles of ethylene oxide per mole of phenol; nonylphenol condensed with 9 moles of ethylene oxide per mole of nonylphenol and di-iso-octylphenol condensed with 5 moles of ethylene oxide.
2. The condensation product of primary or secondary aliphatic alcohols having from 8 to 24 carbon atoms, in either straight chain or branched chain configuration, with from 1 to about 40 moles of alkylene oxide per mole of alcohol. Preferably, the aliphatic alcohol comprises between 9 and 15 carbon atoms and is ethoxylated with between 2 and 9 desirably between 3 and 8 moles of ethylene oxide per mole of aliphatic alcohol. Such nonionic surfactants are preferred from the point of view of providing good to excellent detergency performance on fatty and greasy soils, and in the presence of hardness sensitive anionic surfactants such as alkyl benzene sulphonates. 0000225 preferred surfactants arc prepared from primary alcohols which are either linear (such as those derived) from natural fats of prepared by the Ziegler process from ethylene, eg. myristyl, cetyl, stearyl alcohols), or partly branched such as the Dobanols and Neodols which have about 25% 2-methyl branching (Dobanol and Neodol being Trade.Names of Shell) or Synperonics, which are understood to have about 50% 2-methyl branching (Synperionic is a trade name of I.C.I.) or the primary alcohols having more than 50% branched chain structure sold under the Trade Name Lial by Liquichimica. Specific examples of nonionic surfactants falling within the scope of the invention include Dobanol 45-4, Dobanol 45-7, Dobanol 45-11, Dobanol 91-3, Dobanol 91-6, Dobanol 91-8, Synperonic 6, Synperonic 14, the condensation products of coconut alcohol with an average of between 5 and 12 moles of ethylene oxide per mole of alcohol, the coconut alkyl portion having from 10 to 14 carbon atoms, and the condensation products of tallow alcohol with an average of between 7 and 12 moles of ethylene oxide per mole of alcohol, the tallow portion comprising essentially between 16 and 22 carbon atoms. Secondary linear alkyl ethoxylates are also suitable in the present compositions, especially those ethoxylates of the Tergitol series having from about 9 to 16 carbon atoms in the alkyl group and up to about 11, especially from about 3 to 9, ethoxy residues per molecule.
3. The compounds formed by condensing ethylene oxide with a'hydrophobic base formed by the condensation of propylene oxide with propylene glycol. The molecular weight of the hydrophobic portion generally falls in the range of about 1500 to 1800. Such synthetic nonionic detergents are available on the market under the trade name of "Pluronic" supplied by Wyandotte Chemicals Corporation.

A highly preferred mixture of surfactants is a mixture of a C₈-C₂₂ alkyl benzene sulfonate and a C₉-C₁₅ alkanol ethoxylated with from 3 to 8 moles of ethylene oxide per mole of alkanol. Highly preferred mixtures include C₁₂ alkyl benzene sulfonate and C₁₄-C₁₅ alcohol-(7)-ethoxylate, in ratios of from 2:1 to 1:10, preferably 1:1 to 1:8. In still more preferred compositions, C₈-C₂₄ alkanol ethoxylate with from 10 to 40 moles of ethylene oxide per mole of alkanol is added to the above-described mixture, preferably at a level of from 1% to 5%. The Builder
The Detergent composition of the invention also contains at least about 10% of a detergency builder, especially a water-soluble inorganic or organic electrolyte. Suitable electrolytes have an equivalent weight of less than 210, especially less than 100 and include the common alkaline polyvalent calcium ion sequestering agents. The builder can also include water-insoluble calcium ion exchange materials, however, Non-limiting examples of suitable water-soluble, inorganic detergent builders include: alkali metal carbonates, borates, phosphates, polyphosphates, bicarbonates, silicates, sulfates and chlorides. Specific examples of such salts include sodium and potassium tetraborates, perborates, bicarbonates, carbonates, tripolyphosphates, orthophosphates, pyrophosphates, hexametaphosphates and sulfates.
Examples of suitable organic alkaline detergency builders include: (1) water-soluble amino carboxylates and amino- polyacetates, for example, sodium and potassium glycinates, ethylenediamine tetraacetates, nitrilotriacetates, and N-(2-hydroxyethyl)nitrilo diacetates and diethylenetriamine pentaacetates; (2) water-soluble salts of phytic acid, for example, sodium and potassium phytates; (3) water-soluble polyphosponates, including sodium, potassium, and lithium salts of ethane-1-hydroxy-1,1-diphosphonic acid; sodium, potassium, and lithium salts of ethylene diphosphonic acid; and the like.
(4) water-soluble polycarboxylates such as tnc salts of lactic acid, succinic acid, malonic acid, maleic acid, citric acid, carboxymethyloxysuccinic acid, 2-oxa-1,1,3-propane tricarboxylic acid, 1,1,2,2-ethane tetracarboxylic acid, cyclopentane-cis, cis, cis - tetracarboxylic acid, mellitic acid and pyromellitic acid; (5) water-soluble organic amines and amine salts such as monoethanolamine, diethanolamine and triethanolamine and salts thereof.
Mixtures of organic and/or inorganic builders can be used herein. One such mixture of builders is disclosed in Canadian Patent No. 755.038, e.g. a ternary mixture of sodium tripolyphosphate, trisodium nitrilotriacetate, and trisodium ethane-1-hydroxy-1,1-diphosphonate.
Another type of detergency builder material useful in the present compositions and processes comprises-a water-soluble material capable of forming a water-insoluble reaction product with water hardness cations preferably in combination with a crystallization seed which is capable of providing growth sites for said reaction product. Such "seeded builder" compositions are fully disclosed in British Patent Specification No. 1,424,406.
A further class of detergency builder materials useful in the present invention are insoluble sodium aluminosilicates, particularly those described in Belgium Patent 814,874, issued November 12, 1974, incorporated herein by reference. This patent discloses and claims detergent compositions containing sodium aluminosilicates having the, formula
wherein z and y are integers equal to at least 6, the molar ratio of z to y is in the range of from 1.0:1 to about 0.5:1, and X is an integer from about 15 to about 264, said aluminosilicates having a calcium ion exchange capacity of at least 200 milligrams equivalent/gram and a calcium ion exchange rate of at least about 2 grains/gallon/minute/gram. A preferred material is

Additional Ingredients

The compositions of the present invention can be supplemented by all manner of detergent components, either by including such components in the aqueous slurry to be dried or by admixing such components with the compositions of the invention following the drying step. Soil suspending agents at about 0.1% to 10% by weight such as water-soluble salts of carboxymethyl-cellulose, carboxyhydroxymethyl cellulose, and polyethylene glycols having a molecular weight of about 400 to 10,000 are common components of the present invention. Dyes, pigment optical brighteners, and perfumes can be added in varying amounts as desired.
Other materials such as fluorescers, enzymes in minor amounts, anti-caking agents such as sodium sulfosuccinate, and sodium benzeate can also be added. Enzymes suitable for use herein include those discussed in U.S. Patents 3,519,570 and 3,533,139 to McCarty and McCarty et al issued July 7, 1970 and January 5, 1971, respectively.
Anionic fluorescent brightening agents are well-known materials, examples of which are disodium 4,4'-bis-(2-diethanolamino-4-anilino - s - triazin - 6 - ylamino)stilbene-2:2' disulphonate, disodium 4,4'-bis-(2-morpholino-4-anilino-s-triazin-6-ylaminostilbene-2:2'- disulphonate, disodium 4,4' -bis-(2,4-dianilino-s-triazin-6-ylamino)stilbene-2:2' -disulphonate, disodium 4,4' -bis-(2-anilino-4-(N-methylN-2-hydroxyethylamino)-s-triazin. -6-ylamino)stilbene-2,2' -disulpnonate, disodium 4,4' -bis-(4-phenyl-2,1,3-triazol-2-yl)-stilbene-2,2'disulphonate, disodium 4,4'bis(2-anilino-4-(1-methyl-2-hydroxyethylamino)-s-triazin-6-ylamino)stilbene-2,2' disulphonate and sodium 2(stilbyl-4'' -(naphtho-1',2':4,5)-1,2,3 - triazole-2'' -sulphonate.
An alkali metal, or alkaline earth metal, silicate can also be present. The alkali metal silicate preferably is used in an amount from 0.5% to 10% preferably from 3% to 8%. Suitable silicate solids have a molar ratio of SiO₂/alkali metal₂O in the range from about 0.6 to about 4.0, but much more preferably from 1.0 to 1.8, especially about 1.6. The alkali metal silicates suitable herein can be commercial preparations of the combination of silicon dioxide and alkali metal oxide, fused together in varying proportions.
The compositions of this invention can require the presence of a suds regulating or suppressing agent.
Suds regulating components are normally used in an amount from about 0.001% to about 5%, preferably from about 0.05% to about 3% and especially from about 0,10% to about 1%. The suds suppressing (regulating) agents which are known to be suitable as suds suppressing agents in detergent context can be used in the compositions herein. These include the silicone suds suppressing agents, especially the mixtures of silicones and silica described in U.S. Patent No. 3,933,672, the disclosure of which is incorporated herein by reference. A particularly preferred suds suppressor is the material known as "HYFAC", the sodium salt of a long-chain (C₂₀-C₂₄) fatty acid.
Microcrystalline waxes having a melting point in the range from 35⁰C-115⁰C and saponification value of less than 100 represent an additional example of a preferred suds regulating component for use in the subject compositions. The microcrystalline waxes are substantially water-insoluble, but are water-dispersible in the presence of organic surfactants. Preferred microcrystalline waxes having a melting point from about 65°C to 100°C, a molecular weight in the range from 400-1000; and a penetration value of at least 6, measured at 77°C by ASTM-D1321. Suitable examples of the above waxes include microcrystalline and oxidized microcrystalline petrolatum waxes; Fischer-Tropsch and oxidized Fischer-Tropsch waxes; ozokerite; ceresin; montan wax; beeswax; candelilla; and carnauba wax.
. The granular detergent compositions herein can also advantageously contain a peroxy bleaching component in an amount from about 3% to about 40% by weight, preferably from about 8% to about 33% by weight. Examples of suitable peroxy bleach components for use herein include perborates, persulfates, persilicates, perphosphates, percarbonates, and more in general all inorganic and organic peroxy bleaching agents which are known to be adapted for use in the subject compositions. The composition can also advantageously include a bleach activator which is normally an organic compound containing an N-acyl, or an O-acyl (preferably acetyl) group. Preferred materials are N,N,N' ,N'-tetraacetyl ethylene diamine and N,N,N' ,N'-tetraacetylglycouril.
A further preferred ingredient of the instant compositions is from about 0.01 to about 4%, especially from about 0.5 to about 2.2% by weight of a polyphosphonic acid or salt thereof which is found to provide bleachable stain detergency benefits.
Especially preferred polyphosphonates have the formula:
wherein each R is CH₂PO₃H₂ or a water-soluble salt thereof and n is from O to 2. Examples of compounds within this class are aminotri-(methylenephosphonic acid), aminotri-(ethylidenephosphonic acid), ethylene diamine tetra (methylenephosphonic acid) and diethylene triamine penta (methylene phosphonic acid). Of these, ethylene diamine tetra(methylene phosphonic acid) is particularly preferred.
A further optional, though preferred component is from about 0.1% to.about 3%, especially from about 0.25% to about 1.5% of a polymeric material having a molecular weight of from 2000 to 2,000,000 and which is a copolymer of maleic acid or anhydride and a polymerisable monomer selected from compounds of formula:
wherein R₁ is CH₃ or a C₂ to C₁₂ alkyl group;
wherein R₂ is H or CH₃ and R₃ is H, or a C₁ to C₁₀ alkyl group;
wherein each of R₄ and R₅ is H or an alkyl group such that R₄ and R₅ together have 0 to 10 carbon atoms;

and (vi) mixtures of any two or more thereof, said copolymers being optionally whelly or partly neutralised at the carboxyl groups by sodium or potassium.
Highly preferred examples of such carboxylates are 1:1 styrene/maleic acid copolymer, di-isobutylene/maleic acid copolymers and methyl vinyl ether/maleic acid copolymers.
Other suitable polycarboxylates are poly-a-hydroxy acrylic acids of the general formula
wherein R₁ and R₂ each represent a hydrogen atom or an alkyl group containing 1, 2 or 3 carbon atoms and wherein n represents an anteger greater than 3. Such materials may be prepared as described in Belgium Patent 817,678. Also are poly- lactones prepared from the hydroxy acids as described in British Patent 1,425,307.
In a process aspect of the
there is provided a method of making the detergent composition of the invention comprising the steps of spray drying a crutcher mix' containing the anionic, cationic and builder components and subsequently absorbing the nonionic surfactant in liquid or molten form into the spray-dried granules. This process is particularly valuble when the builder comprises an aluminosilicate ion-exchange material.
In another process aspect.of particular applicability to compositions comprising aluminosilicate builder, the nonionic is included in the crutcher mix for spray drying, but the components of the surfactants are premixed before addition of the aluminosilicate.
Other processes of making the compositions of the invention can be employed, of course. Thus the anionic and nonionic surfactants and the builder and filler components can be spray dried in conventional manner to form a base powder composition and the cationic component can then be added to the base powder either as an approximately 1:1 mixture with part of the builder or filler components retained for that purpose, or as an inclusion complex of, for instance, urea. Alternatively, the cationic surfactant can be sprayed onto the base powder, or added as a dry mixed prill agglo- meratedwith an inorganic or organic agglomerating aid, or can be separately spray dried and added to the base powder as a dry mixed granule. Alternatively, the cationic surfactant and base powder compositions can be individually spray dried in separate stages of a multi-stage spray drying tower.
The compositions of the invention can also be provided in the form of two or more component products, which arc either mixed before use or added separately to a laundry solution to provide a concentration of the ternary surfactant system of from about 100 to about 3000 p.p.m., especially from about 500 to about 1500 p.p.m. Each component product includes one or more of the active ingredients of the ternary surfactant system and a mixture of the products in prescribed amounts should have the requisite granular form. In a preferred embodiment, one product is formulated as a conventional anionic or nonionic detergent composition suitable for use in the main washcycle of an automatic laundry or washing machine, and the other is formulated as a cationic containing additiv or booster product for use simultaneously with the conventional detergent during the main wash. In addition to the cationic, the additive product will contain nonionic and/or anionic surfactant such that the total composition formed by mixing the component products in specified amounts has the requisite ternary active system.
The compositions of the invention can also be formulated as special prewash compositions designed for used before the main.wash stage of the conventional laundering cycle. Such prewash composition will normally consist of a single product component containing the defined ternary active system.
In the Examples which follow, the abbreviations used have the following designations:

LAS : Linear C₁₂ alkyl benzene sulfonate
. TAS : Tallow alkyl sulfate
TAE_n : Tallow alcohol ethoxylated with n moles of ethylene oxide per mole alcohol
MTMAC :' Myristyl trimethyl ammonium chloride
LTMAC : Lauryl trimethylammonium chloride
Dobanol 45-E-7: A C ₁₄-C ₁₅ oxo-alcohol with 7 moles of ethylene oxide, marketed by Shell
Dobanol 45-E-3: A C₁₄-C₁₅ oxo-alcohol with 3 moles of ethylene oxide, marketed by Shell.
Silicate . Sodium silicate having an Si0₂:Na₂0 ratio of 1.6.
Wax: Microcrystalline wax - Witcodur 272 M.pt 87°C
.Silicone : Comprising 0.14 parts'by weight of an 85:15 by weight mixture of silanated silica and silicone, granulated with 1.3 parts of sodium tripolyphosphate, and 0.56 parts of tallow alcohol condensed with 25 molar proportions of ethylene oxide.
Gantrez AN119: Trade name for maleic anhydride/vinyl methyl ether copolymer, believed to have an average molecular weic of about 240,000, marketed by GAF. This was prehydrolysed with NaOII before addition.
Brightener: Disodium 4;4' -bis-(2-morpholino-4-anilino-s-triazin -6-ylamino)stilbene-2:2' ;disulphonate.
TAED Tetraacetyl-ethylene diamine
Dequest.2060 Trade name for diethylene triamine penta (methylene phosphonic acid,) marketed by Monsanto
Dequest2040 : : Trade Name for ethylenediamine tetra (metlylene phosphonic acid,) marketed by Monsanto.

The present invention is illustrated by the following non-limiting examples.

EXAMPLES 1-5

The following compositions were prepared by spray-drying an aqueous slurry of the ingredients except for the Dobanol derived nonicnic surfactants which were sprayed onto the spray-dried granules, and the sodium perborate and enzyme which were dry mixed into the composition.
These products provide enhanced oil and greasestain These products provide enhanced oil and grease removal performance with detriment to particle clay soil detergency, whiteness maintenanceand fluorescer brightening characteristics on both natural and man-made fabrics at both high and low wash temperatures.
Products with enhanced performance are also obtained when the sodium alkyl benzene sulphonate is replaced by molar equivalents of C_1C-C₂₂clefinesulphonates, C₁₀-C₂₀paraffin sulphonates, and C₁₀-C₂₀alkylether sulphates.
The lauryl or myristyl trimethyl ammonium chloride in the above examples can be replaced by molar equivalnets of lauryl or myristyl-trimethyl ammonium bromide, decyl trimethyl ammonium chloride, dioctyl dimethyl ammonium bromide, coconut alkyl benzyl dimethyl ammonium chloride, C₁₂ alkylbenzyl dimethyl ethyl ammonium chloride, C₁₂ alkylbenzyl trimethyl ammonium chloride or one of the following compounds -

EXAMPLES 6-11

The following compositions were prepared similarly to Examples 1-5.
Products with enhanced performance are also
the Dobanol 45-E-7 is replaced by a C_14-15alcohol polyethoxylate containing an average of 6 moles of ethylene oxide, a C_12-15 alcohol polyethoxylate containing an'average .of 6 . 5 moles of ethylene oxide, a C_9-11 alcohol polyethoxylate containing an average of 6 moles of ethylene oxide, a C_12-13 alcohol polyethoxylate containing an average of ₅ moles of ethylene oxide stripped so as to remove lower ethoxylate and unethoxylated fractions, a secondary C₁₅ alcohol polyethoxylate containing an average of 9 moles of ethylene oxide, a C12 alcohol polyethoxylate containing an average of 5 moles of ethylene oxide, a C₁₀ alcohol polyethoxylate containins an average of 5 moles of ethylene oxide, a C₁₄ alcohol polyethoxylate containing an average of 6 moles of ethylene oxide, a C₁₂ alcohol polyethoxylate containing an average of 7 moles of ethylene oxide, and mixtures of those surfactants.
Enhanced performance is also obtained when Gantrez AN 119 is replaced by, as their sodium salts, a copolymer of methyl methacrylate and maleic acid, the molar ratio of the monomers being about 1:1, of molecular weight about 10,000; an ethylene-maleic acid copolymer of molecular weight about 4,000, a propylene-maleic acid copolymer of molecular weight about 30,000; 1-hexene-maleic acid copolymer of molecular weight about 30,000; 1-hexene-maleic acid copolymer of molecular weight about 25,000; a vinyl pyrrolidone-maleic acid copolymer of molecular weight about 26,000 a styrene-maleic acid copolymer of acrylic acid and itaconic acid; a 1:4 copolymer of 3-butenoic acid and methylenemalonic acid; a 1:1.9 copolymer of methacrylic acid and aconitic acid; and a 1.2:1 copolymer of 4-pcntenoic acid and itaconic acid.
Products with enhanced performance are also obtained when the sodium alkyl benzene sulphonate is replaced by molar equivalents of C_1C-C₂₂ olefine sulphonates, C₁₀-C₂₀ paraffin sulphonates, and C₁₀-C₂₀ alkyl ether sulphates.
The- myristyl trimethyl ammonium chloride in the above examples can be replaced by molar equivalnets of lauryl or myristyl-trimethyl ammonium bromide, decyl trimethyl ammonium chloride, dioctyl dimethyl ammonium bromide, coconut alkyl benzyl dimethyl ammonium chloride, C₁₂ , alkylbenzyl dimethyl ethyl ammonium chloride, C₁₂ alkylbenzyl trimethyl ammonium chloride or one of the following compounds

Claims

1. A solid particulate detergent composition comprising

(a) from of a surfactant system comprising a water-soluble or water-dispersible combination of anionic, alkoxylated nonionic and water-soluble quaternary ammonium cationic surfactants, wherein the anionic:cationic surfactant weight ratio is no 'more than5:1and the nonionic:cationic surfactant weight ratio is at least 2:3, and wherein the surfactant system contains anionic and cationic surfactants in an equivalent ratio of at least 1:1, and

(b) at least 10% of a detergency builder

2. A composition according to Claim 1 wherein the cationic surfactant comprises from 1 to 4 quaternary ammonium groups of which only one has the general formula

wherein each R¹ is a hydrophobic alkyl or alkenyl group optionally substituted or interrupted by phenyl, ether, ester or amide groups totalling from 8 to 20 carbon atoms and which may additionally contain up to 20 ethoxy groups, m is a number from 1 to 3 and no more than one R can have more than 16 carbon atoms when m is 2 and no more than 12 carbon atoms when m is 3, each R² is an alkyl group containing from one to four carbon atoms or a benzyl groupwith no more than one R² in a molecule being benzyl and x is from 0 to 3.

3. A composition according to Claim 2 wherein the cationic surfactant has the general formula

wherein R¹ isselected from C₈-C₂₀ alkyl, alkenyl and alkaryl groups R² is selectedfrom C_1-4alkyl and benzyl groups; Z is all anion in number to give electrical neutrality; and m is 1, 2 or 3; provided that when in is 2, R¹ has less than 15 carbons atoms and when m is 3 , R¹ has less than 9 carbon atoms.

4. A composition according to any preceding claim wherein the cationic and anionic surfactant have a combined total of no more than 34 carbon atoms numbered in hydrophobic groups having at least 4 consecutive carbon atoms.

5. A composition.according to any preceding claim wherein the nonionic surfactant has the general formula RO(CH₂CH₂0) _nH wherein R is branched or unbranched C₉-C₁₅ alkyl or alkenyl and n is from 2 to 9.

6. A composition according to any preceding claim wherein the nonionic:cationic surfactant weight-ratio is from 20:1 to 1:1.

7. A composition according to any preceding claim wherein the anionic:cationic surfactant weight ratio is from 2:1 to 1:2.

8. A composition according to any preceding claim wherein the surfactant system comprises at least 5% by weight of the cationic surfactant and at least 60% by weight in total of the anionic and nonionic surfactants.

9. A composition according to any preceding claim wherein the detergency builder comprises a water-soluble inorganic or organic electrolyte having an equivalent weight of no more than 210.

10. A composition according to any preceding claim wherein the detergency builder comprises a water-soluble alkaline polyvalent inorganic or organic calcium ion sequestering agent.

. 11, A composition according to any preceding claim wherein the detergency builder comprises a water-insoluble aluminosilicate ion exchange material of the general formula:

wherein M is a calcium-exchange cation; 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; said aluminosilicate ion exchange material having a particle size diameter from about 0.1 micron to about 100 microns; a calcium ion exchange capacity of at least about 200 mq. eq. CaC0₃/g; and a calcium ion exchange ratio of at least about 2 grains (Ca⁺⁺)/gallon/minute/gram.

12, A composition according to any preceding claim additionally comprising from 0.01 to 2% of an anionic fluoresce