CA2091418A1 - Linear viscoelastic aqueous liquid automatic dishwasher detergent composition - Google Patents

Abstract

Automatic dishwasher detergent composition is formulated as a linear viscoelastic, pseudoplastic, gel-like aqueous product of exceptionally good physical stability, low bottle residue, low cup leakage, and improved cleaning performance, Linear viscoelasticity and pseudoplastic behavior is attributed by incorporation of cross-linked high molecular weight polyacrylic acid type thickener. Control of incorporated air bubbles functions to provide the product with a bulk density of about 1.28 to 1.42 g/cc which roughly corresponds to the density of the liquid phase. Stearic acid or other fatty acid or salt further improve physical stability.

Description

2091 ~1 8 IR-4681A-l L ~ ~ VT~m~
LIQUID AUTOMP~Tr nTe~ ~vD
n~ N~-rQr~ oN~-Field of Invention The present invention relates generally to an automatiedishwasher detergent composition in the form of an aqueous lineAr viseoelastic liquid.
Baekqround of the Invention Liquid automatie dishwasher detergent c~ -itions, both aqueous and nonaqueous, have reeently reeeived mueh attention, and the aqueous products have achieved commereial popularity.
The aeeeptanee and popularity of the liquid formulations as compared to the more conventional powder produets stems from the convenienee and performanee of the liquid produets.
However, even the best of the currently available liquid formulations still suffer from two major problems, produet phase instability and bottle residue, and to some extent cup leakage from the dispenser cup of the automatie dishwashing ~eh;~e.
Representative of the relevant patent art in this area, mention is made of Rek, U.S. Patent 4,556,504; Bush, et al., U.S. Patent 4,226,736; Ulrich, U.S. Patent 4,431,5S9;

Sabatelli, U.S. Patent 4,147,650; Paucot, U.S. Patent 4,079,015; Leikhem, U.S. Patent 4,116,849; Milora, U.S. Patent 4,521,332; Jones, U.S. Patent 4,597,889; Heile, U.S. Patent 4,512,908; Laitem, U.S. Patent 4,753,748; Sabatelli, U.S.
Patent 3,579,455; Hynam, U.S. Patent 3,684,722: other patents relating to thickened detergent compositions include U.S.
Patent 3,985,668; U.K. Patent Applications GB 2,116,199A and GB 240,450A; U.S. Patent 4,511,487; U.S. Patent 4,752,409 (Drapier, et al.); U.S. Patent 4,801,395 (Drapier, et al.);
U.S. Patent 4,801,395 (Drapier, et al.). Cnm~ly assigned co-pending patents include, for example, Serial No. 204,476 filed June 9, 1988; Serial No. 924,385, filed October 29, 1986; Serial No. 323,138, filed March 13, 1989; Serial No.
087,836, filed August 21, 1987; Serial No. 328,716, filed March 27, 1989; Serial No. 323,137, filed March 13, 1989;
Serial No. 323,134, filed March 13, 1989.
The present invention provides a solution to the above problems.

Brief Description of the Drawings Figures 1-13 are rheograms, plotting elastic modules G' and viscous modulus G" as a function of applied strain, for the compositions of Example 1, Formulations A, C, D, G, J, H, I and K, Example 2, A and B, Example 3, L and M and Comparative Example 1, respectively.

2 ~ 9 1 4 1 8 62301-1821 .

Summary of the Invention According to the present invention there is provided a novel aqueous liquid automatic dishwasher detergent composi-tion. The composition is characterized by its linear visco-elastic behavior, substantially indefinite stability against phase separation or settling of dissolved or suspended particles, low levels of bottle residue, relatively high bulk density, and substantial absence of unbound or free water. The composition does not exhibit phase separation and remains homogeneous when it is centrifused at 1,000 rpm for 30 minutes.
This unique combination of properties is achieved by virtue of the incorporation into the aqueous mixture of alkali metal detergent builder salt(s) and chlorine bleach compound, a small but effective amount of high molecular weight cross-linked polyacrylic acid type thickening agent, and a source of potassium ions to provide a potassium/sodium weight ratio in the range of from about 1:1 to about 1:30, such that substantially all of the detergent builder salts and other normally solid detergent additives present in the composition are present dissolved in the aqueous phase. The compositions are further characterized by a bulk density of from about 1.26 g/cm to about 1.42 g/cm3 such that the density of the polymeric phase and the density of the aqueous (continuous) phase are approximately the same.
Detailed Description of the Preferred Embodiments The compositions of this invention are aqueous liquids containing various cleansing active ingredients, thickening agents and stabilizing components, although some ingredients may serve more than one of these functions.
The advantageous characteristics of the compositions of this invention, including physical stability, low bottle residue, high cleaning performance, e.g. low spotting and filming, dirt residue removal, and so on, and superior aesthetics, are believed to be attributed to several interrelated factors such as low solids, i.e. llnAiscolved particulate content, product density and linear viscoelastic rheology. These factors are, in turn, dependent on several critical compositional components of the formulations, namely, (1) the inclusion of a thickening effective amount of polymeric thickening agent having high water absorption capacity, exemplified by high molecular weight cross-linked polyacrylic acid, (2) inclusion of a physical stabilizing amount of a long chain fatty acid or salt thereof, (3) potassium ion to sodium ion weight ratio K/Na in the range of from about 1:1 to 1:30, especially from 1.05:1 to 1:10, and (4) a product bulk density of at least about 1.26 glcc, such that the bulk density and liquid phase density are about the same.
The polymeric thickening agents contribute to the linear viscoelastic rheology of the invention compositions. As used herein, "linear viscoelastic "or" linear viscoelasticity"
means that the elastic (storage) moduli (G') and the viscous (loss) moduli (G") are both substantially independent of strain, at least in an applied strain range of from 0-50%, and preferably over an applied strain range of from 0-80%. More - 2091~18 specifically, a composition is considered to be linear viscoelastic for purposes of this invention, if over the strain range of 0-50% the elastic moduli G~ has a min;mllm value of 100 dynes/sq.cm., preferably at least 250 dynes/sq.cm., and varies less than about 500 dynes/sq.cm, preferably less than 300 dyneslsq.cm., especially preferably less than 100 dynes/sq.cm. Preferably, the m; n; mllm value of G' and maximum variation of G' applies over the strain range of 0 to 80%. Typically, the variation in loss moduli G" will be less than that of G'. As a further characteristic of the preferred linear viscoelastic compositions the ratio of G"/G
(tanS) is less than 1, preferably less than 0.8, but more than O.OS, preferably more than 0.2, at least over the strain range of 0 to 50%, and preferably over the strain range of 0 to 80%.
It should be noted in this regard that % strain is shear strain xlO0.
By way of further explanation, the elastic (storage) modulus G' is a measure of the energy stored and retrieved when a strain is applied to the composition while viscous (loss) modulus G" is a measure to the amount of energy dissipated as heat when strain is applied. Therefore, a value of tan~
0.05< tan ~ <1, preferably 0.2 < tan~ < 0.8 means that the compositions will retain sufficient energy when a stress or strain is applied, at least over the extent expected to be encountered for products of this type, for 2~91418 - example, when poured from or shaken in the bottle, or stored in the dishwasher detergent dispenser cup of an automatic dishwashing machine, to return to its previous condition when the stress or strain is removed. The compositions with tan values in these ranges, therefore, will also have a high cohesive property, namely, when a shear or strain is applied to a portion of the composition to cause it to flow, the surrounding portions will follow. As a result of this cohesiveness of the subject linear viscoelastic compositions, the compositions will readily flow uniformly and homogeneously from a bottle when the bottle is tilted, thereby contributing to the physical (phase) stability of the formulation and the low bottle residue (low product loss in the bottle) which characterizes the invention compositions. The linear viscoelastic property also contributes to improved physical stability against phase separation of any undissolved suspended particles by providing a resistance to movement of the particles due to the strain exerted by a particle on the surrounding fluid medium.
Also contributing to the physical stability and low bottle residue of the invention compositions is the potassium to sodium ion ratios in the range of 1:1 to 1:30, preferably 1:1 to 20:1, especially preferably from 1.05:1 to 1:10.
A still further attribute of the invention compositions contributing to the overall product stability and low bottle residue is the high water absorption capacity of the cross-linked polyacrylic acid type thickening agent. As a result of this high water absorption capacity virtually all of the - ~ 2031418 aqueous vehicle component is held tightly bound to the polymer matrix. Therefore, there is no or substantially no free water present in the invention compositions. This absence of free water (as well as the cohesiveness of the composition) is manifested by the observation that when the composition is poured from a bottle onto a piece of water absorbent filter paper virtually no water is absorbed onto the filter paper and, furthermore, the mass of the linear viscoelastic material poured onto the filter paper will retain its shape and structure until it is again subjected to a stress or strain.
As a result of the absence of unbound or free water, there is virtually no phase separation between the aqueous phase and the polymeric matrix or dissolved solid particles. This characteristic is manifested by the fact that when the subject lS compositions are subjected to centrifugation, e.g. at 1000 rpm for 30 minutes, there is no phase separation and the composition r~mA; ns homogeneous.
However, it has also been discovered that linear viscoelasticity and K/Na ratios in the above-mentioned range do not, by themselves, assure long term physical stability (as determined by phase separation). In order to m~xi~ize physical (phase) stability, the density of the composition should be controlled such that the bulk density of the liquid phase is approximately the same as the bulk density of the entire composition, including the polymeric thicke~ing agent.
This control and equalization of the densities is achieved, according to the invention, by providing the composition with a bulk density of at least 1.26 g/cc, preferably at least 1.32 -- ~. 2091~18 g/cc, up to about 1.42 g/cc, preferably up to about 1.40 g/cc.
Furthermore, to achieve these relatively high bulk densities, it is important to mi n;m; ze the amount of air incorporated into the composition (a density of about 1.42 g/cc is essentially equivalent to zero air content).
It has previously been found in connection with other types of thickened aqueous liquid, automatic dishwasher detergent compositions that incorporation of finely divided air bubbles in amounts up to about 8 to 10% by volume can function effectively to stabilize the composition against phase separation, but that to prevent agglomeration of or escape of the air bubbles it was important to incorporate certain surface active ingredients, especially higher fatty acids and the salts thereof, such as stearic acid, hehen;c acid, palmitic acid, sodium stearate, aluminum stearate, and the like. These surface active agents apparently functioned by forming an interfacial film at the bubble surface while also forming hydrogen bonds or contributing to the electrostatic attraction with the suspended particles, such that the air bubbles and attracted particles formed agglomerates of approximately the same density as the density of the continuous liquid phase.
Therefore, in a preferred emboA;m~nt of the present invention, stabilization of air bubbles which may become 2~ incorporated into the compositions during normal processing, such as during various mixing steps, is avoided by post-adding the surface active ingredients, including fatty acid or fatty acid salt stabilizer, to the rem~;nAer of the composition, - - - - -r-~ 2 091 ~ 1 8 under low shear conditions using mix;ng devices designed to m;ni~ize cavitation and vortex formation.
As will be described in greater detail below the surface active ingredients present in the composition will include the main detergent surface active cleaning agent, and will also preferably include anti-foaming agent and higher fatty acid or salt thereof as a physical stabilizer.
Exemplary of the cross-linked polyacrylic acid-type thickening agents are the products sold by B.F. Goodrich under their Carbopol trA~em~rk, especially Carbopol 941, which is the most ion-insensitive of this class of polymers, and Carbopol 940 and Carbopol 934. The Carbopol resins, also known as "Carbomer", are hydrophilic high molecular weight, cross-linked acrylic acid polymers having an average equivalent weight of 76, and the general structure illustrated by the following formula:
H H
C- C
l l H C n.
HO O

Carbopol 941 has a molecular weight of about 1,250,000;
Carbopol 940 a molecular weight of approximately 4,000,000 and Carbopol 934 a molecular weight of approximately 3,000,000.
The Carbopol resins are cross-linked with polyalkenyl polyether, e.g. about 1% of a polyallyl ether of sucrose having an average of about 5.8 allyl groups for each molecule of sucrose. Further detailed information on the Carbopol --- -r-~ 2 0 9 1 1 1 8 resins is available from B.F. Goodrich, see, f or example, the B.F. Goodrich catalog GC-67, Carbopol~ Water Soluble Resins.
While most f avorable results have been achieved with Carbopol 941 polyacrylic resin, other lightly cross-linked polyacrylic acid-type thickening agents can also be used in the compositions of this invention. As used herein "polyacrylic acid-type" refers to water-soluble homopolymers of acrylic acid or methacrylic acid or water-dispersible or water-soluble salts, esters or amides thereof, or water-soluble copolymers of these acids of their salts, esters or ameides with each other or with one or more other etylenically unsaturated monomers, such as, for example, styrene, maleic acid, maleic anhydride, 2-hydroxyethylacrylate, acrylonitrile, vinyl acetate, ethylene, propylene, and the like.
The homopolymers or copolymers are characterized by their high molecular weight, in the range of from about 500,000 to 10,000,000, preferably 500,000 to 5,000,000, especially from about 1,000,000 to 4,000,000, and by their water solubility, generally at least to an extent of up to about 5% by weight, or more, in water at 25~C.
These thickening agents are used in their lightly cross-linked form wherein the cross-linking may be accomplished by means known in the polymer arts, as by irradiation, or, preferably, by the incorporation into the monomer mixture to be polymerized of known chemical cross-linking monomeric agents, typically polyunsaturated (e.g. diethylenically unsaturated) monomers, such as, for example, divinylbenzene, divinylether of diethylene glycol, N, N'-methylene-r~ 2 0 9 1 4 1 8 bisacrylamide, polyalkenylpolyethers (such as described above~, and the like. Typically, amounts of cross-li nki ng agent to be incorporated in the final polymer may range from about 0.01 to about l.S percent, preferably from about 0.05 to about 1.2 percent, and especially, preferably from about 0.1 to about 0.9 percent, by weight of cross-linking agent to weight of total polymer. Generally, those skilled in the art will recognize that the degree of cross-linking should be sufficient to impart some coiling of the otherwise generally linear polymeric compound while maint~;n;ng the cross-linked polymer at least water dispersible and highly water-swellable in an ionic aqueous medium. It is also understood that the water-swelling of the polymer which provides the desired thickening and viscous properties generally depends on one or two mechanisms, namely, conversion of the acid group cont~;n;ng polymers to the corresponding salts, e.g. sodium, generating negative charges along the polymer backbone, thereby causing the coiled molecules to expand and thicken the aqueous solution; or by formation of hydrogen bonds, for example, between the carboxyl groups of the polymer and hydroxyl donor. The former mechanism is especially important in the present invention, and therefore, the preferred polyacrylic acid-type thickening agents will contain free carboxylic acid (COOH) groups along the polymer backbone.
-25 Also, it will be understood that the degree of cross-l;nk;ng should not be so high as to render the cross-linked polymer completely insoluble or non-dispersible in water or inhibit or ~ 2091 418 prevent the uncoiling of the polymer molecules in the presence of the ionic aqueous system.
The amount of at least one high molecular weight, cross-linked polyacrylic acid or other high molecular weight, hydrophilic cross-linked polyacrylic acid-type thickening agent to impart the desired rheological property of l; neAr viscoelasticity will generally be in the range of from about 0.1 to 2%, preferably from about 0.2 to 1.75%, by weight, based on the weight of the composition, although the amount will depend on the particular cross-linking agent, ionic strength of the composition, hydroxyl donors and the like.
The compositions of this invention must include sufficient amount of potassium ions and sodium ions to provide a weight ratio of K/Na of 1:1 to 1:30. When the K/Na ratio is less than 1 there is less solubility of the normally solid ingredients making a less transcluent composition with acceptable cleaning performance whereas when the K/Na ratio is more 1:1 the composition is a more translucent composition.
When the K/Na ratio is more than 45, especially when it is greater than about 3, the product becomes too liquid and phase separation begins to occur. When the K/Na ratios become much larger than 45, such as in all or mostly potassium formulation, the polymer thickener loses its absorption capacity and begins to salt out of the aqueous phase.
The potassium and sodium ions can be made present in the compositions as the alkali metal cation of the detergent builder salt(s), or alkali metal silicate or alkali metal hydroxide components of the compositions. The alkali metal 20~1 ~18 cation may also be present in the compositions as a component of an ionic detergent, bleach or other ionizable salt compound additive, e.g. alkali metal carbonate. In determining the K/Na weight ratios all of these sources should be taken into consideration.
Specific examples of detergent builder salts include the polyphosphates, such as alkali metal pyrophosphate, alkali metal tripolyphosphate, alkali metal metaphosphate, and the like, for example, sodium or potassium tripolyphosphate (hydrated or anhydrous), tetrasodium or tetrapotassium pyrophosphate, sodium or potassium hexa-metaphosphate, trisodium or tripotassium orthophosphate and the like, sodium or potassium carbonate, sodium or potassium citrate, sodium or potassium nitrilotriacetate, and the like. The phosphate builders, where not precluded due to local regulations, are preferred and mixtures of tetrapotassium pyrophosphate (TKPP) and sodium tripolyphosphate (NaTPP) (especially the hexahydrate) are especially preferred. Typical ratios of NaTPP to TKPP are from about 2:1 to 1:8, especially from about 1:1.1 to 1:6. The total amount of detergent builder salts is preferably from about S to 35% by weight, more preferably from about 15 to 35%, especially from about 18 to 30% by weight of the composition.
In connection with the builder salts are optionally used a low molecular weight noncrosslinked polyacrylates having a molecular weight of about 1,000 to about 100,000, more preferably about 2,000 to about 80,000. A preferred low molecular weight polyacrylate is Norasol LMW45ND manufactured - 2~91~18 by Norsoshaas and having a molecular weight of about 4,500.
These low molecular weight polyacrylates are employed at a concentration of about O to 15 wt.%, more preferably 0.1 to 10 wt.%.
Other useful low molecular weight noncrosslinked polymers are Acusoltm6 4OD provided by Rohm & Haas; Norasol QR1014 from Norsohaas having a GPC molecular weight of 10,000.
The linear viscoelastic compositions of this invention may, and preferably will, contain a small, but stabilizing effective amount of a long chain fatty acid or monovalent or polyvalent salt thereof. Although the manner by which the fatty acid or salt contributes to the rheology and stability of the composition has not been fully elucidated it is hypothesized that it may function as a hydrogen bonding agent or cross-linking agent for the polymeric thickener.
The preferred long chain fatty acids are the higher aliphatic fatty acids having from about 8 to 22 carbon atoms, more preferably from about 10 to 20 carbon atoms, and especially preferably from about 12 to 18 carbon atoms, and especially preferably from about 12 to 18 carbon atoms, inclusive of the carbon atom of the carboxyl group of the fatty acid. The aliphatic radical may be saturated or unsaturated and may be straight or branched. Straight chain saturated fatty acids are preferred. Mixtures of fatty acids may be used, such as those derived from natural sources, such as tallow fatty acid, coco fatty acid, soya fatty acid, mixtures of these acids, etc. Stearic acid and mixed fatty acids, e.g. stearic acid/palmitic acid, are preferred.

~ When the free acid form of the fatty acid is used directly it will generally associate with the potassium and sodium ions in the aqueous phase to form the corresponding alkali metal fatty acid soap. However, the fatty acid salts may be directly added to the composition as sodium salt or potassium salt, or as a polyvalent metal salt, although the alkali metal salts of the fatty acids are preferred fatty acid salts.
The preferred polyvalent metals are the di- and tri-valent metals of Groups IIA, IIB and IIIB, such as magnesium, calcium, aluminum and zinc, although other polyvalent metals, including those of Groups IIIA, IVA, VA, IB, IVB, VB, VIB VIIB
and VIII of the Periodic Table of the Elements can also be used. Specific examples of such other polyvalent metals include Ti, Zr, V, Nb, Mn, Fe, Co, Ni, Cd, Sn, Sb, Bi, etc.
Generally, the metals may be present in the divalent to pentavalent state. Preferably the metal salts are used in their higher oxidation states. Naturally, for use in automatic dishwashers, as well as any other applications where the invention composition will or may come in contact with articles used for the h~n~l;ng, storage or serving of food products or which otherwise may come into contact with or be consumed by people or ~nim~lfi, the metal salt should be selected by taking into consideration the toxicity of the -25 metal. For this purpose, the alkali metal and calcium and magnesium salts are especially higher preferred as generally safe food additives.

2091~18 --The amount of the fatty acid or fatty acid salt stabilizer to achieve the desired enhancement of physical stability will depend on such factors as the nature of the fatty acid or its salt, the nature and amount of the thickening agent, detergent active compound, inorganic salts, other ingredients, as well as the anticipated storage and shipping conditions.
Generally, however, amounts of the fatty acid or fatty acid salt stabilizing agents in the range of from about 0 to 2.0%, preferably 0.005 to 2.0%, more preferably from about 0.01 to 2.0%, provide a long term stability and absence of phase separation upon stAn~;ng or during transport at both low and elevated temperatures as are required for a commercially acceptable product.
Depending on the amounts, proportions and types of fatty acid physical stabilizers and polyacrylic acid-type thickening agents, the addition of the fatty acid or salt not only increases physical stability but also provides a simultaneous increase in apparent viscosity. Amounts of fatty acid or salt to polymeric thickening agent in the range of from about 0.005-0.4 weight percent fatty acid salt and from about 0.4-1.75 weight percent polymeric thicken;ng agent are usually sufficient to provide these simultaneous benefits and, therefore, the use of these ingredients in these amounts is most preferred.
In order to achieve the desired benefit from the fatty acid or fatty acid salt stabilizer, without stabilization of excess incorporated air bubbles and consequent excessive 2~1418 lowering of the product bulk density, the fatty acid or salt .should be post-added to the formulation, preferably together with the other surface active ingredients, including detergent active compound and anti-foaming agent, when present. These surface active ingredients are preferably added as an emulsion in water wherein the emulsified oily or fatty materials are finely and homogeneously dispersed throughout the aqueous phase. To achieve the desired fine emulsification of the fatty acid or fatty acid salt and other surface active ingredients, it is usually necessary to heat the emulsion (or preheat the water) to an elevated temperature near the melting temperature of the fatty acid or its salt. For example, for stearic acid having a melting point of 68~C-69~C, a temperature in the range of between 50~C and 70~C will be used. For lauric acid (m.p.=47~C) an elevated temperature of about 35~C to 50~C can be used. Apparently, at these elevated temperatures the fatty acid or salt and other surface active ingredients can be more readily and uniformly dispersed (emulsified) in the form of fine droplets throughout the composition.
In contrast, as will be shown in the examples which follow, if the fatty acid is simply post-added at ambient temperature, the composition is not linear viscoelastic as defined above and the stability of the composition is clearly inferior.
Foam inhibition is important to increase dishwasher machine efficiency and m;~;m; ze destabilizing effects which might occur due to the presence of excess foam within the ;. 2091gl8 washer during use. Foam may be reduce by suitable selection of the type and/or amount of detergent active material, the main foam-producing component. The degree of foam is also somewhat dependent on the hardness of the wash water in the machine whereby suitable adjustment of the proportions of the builder salts such as NaTPP which has a water softening effect, may aid in providing a degree of foam inhibition.
However, it is generally preferred to include a chlorine bleach stable foam depressant or inhibitor. Particularly effective are the alkyl phosphoric acid esters of the formula HO-P-R
ll OR
and especially the alkyl acid phosphate esters of the formula ~
HO-P-OR

OR
In the above formulas, one or both R groups in each type of ester may represent independently a Clz-C20 alkyl or ethoxylated alkyl group. The ethoxylated derivatives of each type of ester, for example, the condensation products of one mole of ester with from 1 to 10 moles, preferably 2 to 6 moles, more preferably 3 or 4 moles, ethylene oxide can also be used. Some examples of the foregoing are commercially available, such as the products SAP from Hooker and LPKN-158 from Knapsack. Mixtures of the two types, or any other chlorine bleach stable types, or mixtures of mono- and di-2~91~18 esters of the same type, may be employed. Especially preferred is a mixture of mono- and di-C1~-C18 alkyl acid phosphate esters such as monostearyl/distearyl acid phosphates 1.2/1, and the 3 to 4 molé ethylene oxide condensates thereof.
When employed, proportions of 0.05 to 1.5 weight percent, preferably 0.1 to 0.5 weight percent, of foam depressant in the composition is typical, the weight ratio of detergent active component (d) to foam depressant (e) generally ranging from about 10:1 to 1:1 and preferably about 5:1 to 1:1. Other defoamers which may be used include, for example, the known silicones, such as available from Dow Chemicals. In addition, it is an advantageous feature of this invention that many of the stabilizing salts, such as the stearate salts, for example, aluminum stearate, when included, are also effective as foam killers.
Although any chlorine bleach compound may be employed in the compositions of this invention, such as dichloro-isocyanurate, dichloro-dimethyl hydantoin, or chlorinated TSP, alkali metal or alkaline earth metal, e.g. potassium, lithium, magnesium and especially sodium, hypochlorite is preferred.
The composition should contain sufficient amount of chlorine bleach compound to provide about 0.2 to 4.0% by weight of available chlorine, as determined, for example by acidification of 100 parts of the composition with excess hydrochloric acid. A solution cont~;n;ng about 0.2 to 4.0% by weight of sodium hypochlorite contains or provides roughly the same percentage of available chlorine. About 0.8 to 1.6% by weight of available chlorine is especially preferred. For - -~xample, sodium hypochlorite (NaOCL) solution of from about 11 to about 13% available chlorine in amounts of about 3 to 20%, preferably about 7 to 12%, can be advantageously used.
Detergent active material useful herein should be stable in the presence of chlorine bleach, especially hypochlorite bleach, and for this purpose those of the organic anionic, amine oxide, phosphine oxide, sulphoxide or betaine water dispersible surfactant types are preferred, the first mentioned anionics being most preferred. Particularly preferred surfactants herein are the linear or branched alkali metal mono- and/or di-(C8-C14) alkyl diphenyl oxide mono-and/or di-sulphates, commercially available for example as DOWFAX (registered trademark) 3B-2 and DOWFAX 2A-1. In addition, the surfactant should be compatible with the other ingredients of the composition. Other suitable organic anionic, non-soap surfactants include the primary alkylsulphates, alkylsulphonates, alkylarylsulphonates and sec.-alkylsulphates. Examples include sodium C1O_C18 alkylsulphates such as sodium dodecylsulphate and sodium tallow alcoholsulphate; sodium Clo-cl8 alkanesulphonates such as sodium hexadecyl-1-sulphonate and sodium C12-Cl8 alkylbenzenesulphonates such as sodium dodecylbenzenesylphonates. The corresponding potassium salts may also be employed.
~5 As other suitable surfactants or detergents, the amine oxide surfactants are typically of the structure R2R1NO, in which each R represents a lower alkyl group, for instance, methyl, and R1 represents a long chain alkyl group having from ~ to 22 carbon atoms, for instance a lauryl, myristyl, palmityl or cetyl group. Instead of an amine oxide, a corresponding surfactant phosphine oxide R2R1PO or sulphoxide RRlSO can be employed. Betaine surfactants are typically of the structure R2R1N+R"COO-, in which each R represents a lower alkylene group having from 1 to 5 carbon atoms. Specific examples of these surfactants include lauryl-dimethylamine oxide, myristyl-dimethylamine oxide, myristyl-dimethylamine oxide, the corresponding phosphine oxides and sulphoxides, and the corresponding betaines, including dodecyldimethylammonium acetate, tetradecyldiethylammonium pentanoate, hexadecyldimethylammonium hexanoate and the like. For biodegradability, the alkyl groups in these surfactants should be linear, and such compounds are preferred.
Surfactants of the foregoing type, all well known in the art, are described, for example, in U.S. Patents 3,985,668 and 4,271,030. If chlorine bleach is not used than any of the well known low-foaming nonionic surfactants such as alkoxylated fatty alcohols, e.g. mixed ethylene oxide-propylene oxide condensates of C8-Cz2 fatty alcohols can also be used.
The chlorine bleach stable, water dispersible organic detergent-active material (surfactant) will normally be present in the composition in minor amounts, generally about 1% by weight of the composition in minor amounts, generally about 1% by weight of the composition, although smaller or larger amounts, such as up to about 5%, such as from 0.1 to - ~---- 2091418 j%, preferably form 0.3 or 0.4 to 2% by weight of the composition, may be used.
Alkali metal (e.g. potassium or sodium) silicate, which provides alkalinity and protection of hard surfaces, such as fine china glaze and pattern, is generally employed in an amount ranging from about 0 to 25 weight percent, preferably about 5 to 15 weight percent, more preferably 8 to 12% in the composition. The sodium or potassium silicate is generally added in the form of an aqueous solution, preferably having Na2O:SiOz or KzO:SiO2 ratio of about 1:1.3 to 1:2.8, especially preferably 1:2.0 to 1:2.6. At this point, it should be mentioned that many of the other components of this composition, especially alkali metal hydroxide and bleach, are also often added in the form of a preli mi n~ry prepared aqueous dispersion or solution.
In addition to the detergent active surfactant, foam inhibitor, alkali metal silicate corrosion inhibitor, and detergent builder salts, which all contribute to the cleaning performance, it is also known that the effectiveness of the liquid automatic dishwasher detergent compositions is related to the alk~li ni ty, and particularly to moderate to high alkalinity levels. Accordingly, the compositions of this invention will have pH values of at least about 9.5, preferably at least about 11 to as high as 14, generally up to about 13 or more, and, when added to the aqueous wash bath at a typical concentration level of about 10 grams per liter, will provide a pH in the wash bath of at least about 9, preferably at least about 10, such as 10.5, 11, 11.5 or 12 or more.
The alkalinity will be achieved, in part by the alkali metal ions contributed by the alkali metal detergent builder salts, e.g. sodium tripolyphosphate, tetrapotassium pyrophosphate, and alkali metal silicate, however, it is usually necessary to include alkali metal hydroxide, e.g. NaOH
or KOH, to achieve the desired high alkalinity. Amounts of alkali metal hydroxide in the range of (on an active basis) of from about 0.5 to 8%, preferably from 1 to 6%, more preferably from about 1.2 to 4%, by weight of the composition will be sufficient to achieve the desired pH level and/or to adjust the K/Na weight ratio.
Other alkali metal salts, such as alkali metal carbonate may also be present in the compositions in minor amounts, for example from 0 to 4%, preferably 0 to 2%, by weight of the composltion .
Other conventional ingredients may be included in these compositions in small amounts, generally less than about 3 weight percent, such as perfume, hydrotropic agents such as the sodium benzene, toluene, xylene and cumene sulphonates, preservatives, dyestuffs and pigments and the like, all of course being stable to chlorine bleach compound and high alk~l; n; ty. Especially preferred for coloring are the chlorinated phythalocyanines and polysuphides of aluminosilicate which provide, respectively, pleasing green and blue tints. TiO2 may be employed for whitening or neutralizing off-shades.

2~91418 , Although for the reasons previously discussed excessive air bubbles are not often desirable in the invention compositions, depending on the amounts of dissolved solids and liquid phase densities, incorporation of small amounts of finely divided air bubbles, generally up to about 10% by volume, preferably up to about 4% by volume, more preferably up to about 2% by volume, can be incorporated to adjust the bulk density to approximate liquid phase density. The incorporated air bubbles should be finely divided, such as up to about 100 microns in diameter, preferably from about 20 to about 40 microns in diameter, to assure maximum stability.
Although air is the preferred gaseous medium for adjusting densities to improve physical stability of the composition other inert gases can also be used, such as nitrogen, carbon dioxide, helium, oxygen, etc.
The amount of water contained in these compositions should, of course, be neither so high as to produce unduly low viscosity and fluidity, nor so low as to produce unduly high viscosity and low flowability, linear viscoelastic properties in either case being ~imi ni shed or destroyed by increasing tan 1. Such amount is readily determined by routine experimentation in any particular instance, generally ranging from 30 to 75 weight percent, preferably about 35 to 65 weight percent. The water should also be preferably deionized or softened.
The manner of formulating the invention compositions is also important. As discussed above, the order of mixing the ingredients as well as the manner in which the mixing is , performed will generally have a significant effect on the properties of the composition, and in particular on product density (by incorporation and stabilization of more or less air) and physical stability (e.g. phase separation). Thus, according to the preferred practice of this invention the compositions are prepared by first forming a dispersion of the polyacrylic acid-type thickener in water under moderate to high shear conditions, neutralizing the dissolved polymer to cause gelation, and then introducing, while continl~;ng mixing, the detergent builder salts, alkali metal silicates, chlorine bleach compound and rem~i~;ng detergent additives, including any previously unused alkali metal hydroxide, if any, other than the surface-active compounds. All of the additional ingredients can be added simultaneously or sequentially.
Preferably, the ingredients are added sequentially, although it is not necessary to complete the addition of one ingredient before beginning to add the next ingredient. Furthermore, one or more of these ingredients can be divided into portions and added at different times. These mixing steps should also be performed under moderate to high shear rates to achieve complete and uniform mixing. These mixing steps may be carried out at room temperature, although the polymer thickener neutralization (gelation) is usually exothermic.
The composition may be allowed to age, if necessary, to cause ~5 dissolved or dispersed air to dissipate out of the composition.
The rem~ining surface active ingredients, including the anti-foaming agent, organic detergent compound, and fatty acid - 2091~18 ~r fatty acid salt stabilizer is post-added to the previously formed mixture in the form of an aqueous emulsion (using from about 1 to 10%, preferably from about 2 to 4% of the total water added to the composition other than water added as carrier for other ingredients or water of hydration) which is pre-heated to a temperature in the range of from about Tm+5 to Tm-20, preferably from about Tm to TM-10, where Tm is the melting point temperature of the fatty acid or fatty acid salt. For the preferred stearic acid stabilizer the heating temperature is in the range of 50~C to 70~C. However, if care is taken to avoid excessive air bubble incorporation during the gelatin step or during the mixing of the detergent builder salts and other additives, for example, by operating under vacuum, or using low shearing conditions, or special mixing operatatus, etc., the order of addition of the surface active ingredients should be less important.
In accordance with an especially preferred embodiment, the thickened linear viscoelastic aqueous automatic dishwasher detergent composition of this invention includes, on a weight basis:
(a) 10 to 35%, preferably 15 to 30%, alkali metal detergent builder salt;
(b) 0 to 25, preferably 15 to 15%, alkali metal silicate;
(c) 0 to 6%, preferably 1 to 6%, alkali metal hydroxide;
(d) 0 to 5%, preferably 0.1 to 3%, chlorine bleach stable, water-dispersible, low-foaming organic detergent active material, preferably non-soap anionic detergent;

2091~18 (e) 0 to 1.5%, preferably 0.1 to 1.5%, chlorine bleach .stable foam depressant;
(f) chlorine bleach compound in an amount to provide about 0.2 to 4%, preferably 0.8 to 1.6%, of available chlorine;
(g) at least one high molecular weight hydrophilic cross-linked polyacrylic acid thickening agent in an amount to provide a linear viscoelasticity to the formulation, preferably from about 0.1 to 2.0%, more preferably from about 0.2 to 1.75%;
(h) a long chain fatty acid or a metal salt of a long chain fatty acid in an amount effective to increase the physical stability of the compositions, preferably from 0 to 2.0%, more preferably from 0.005 to 2.0%; and (i) balance water, preferably from about 30 to 75%, more preferably from about 35 to 65%; and wherein in (a) the alkali metal polyphosphate includes a mixture of from about 5 to 30%, preferably from about 12 to 22% of tetrapotassium pyrophosphate, and from 0 to about 20%, preferably from about 3 to 18% of sodium tripolyphosphate, and wherein in the entire composition the ratio, by weight, of potassium ions to sodium ions is from about 1:1 to 1:30 preferably from 1:1 to 1:20, the compositions having an amount of air incorporated therein such that the bulk density of the composition is from about 1.26 to 1.42 g/cc, preferably from about 1.32 to 1.40 g/cc.
The compositions will be supplied to the consumer in suitable dispenser containers preferably formed of molded plastic, especially polyolefin plastic, and most preferably polyethylene, for which the invention compositions appear to have particularly favorable slip characteristics. In addition to their linear viscoelastic character, the compositions of this invention may also be characterized as pseudoplastic gels (non-thixotropic) which are typically near the borderline between liquid and solid viscoelastic gel, depending, for example, on the amount of the polymeric thickener. The invention compositions can be readily poured from their containers without any shaking or squeezing, although squeezable containers are often convenient and accepted by the consumer for gel-like products.
The liquid aqueous linear viscoelastic automatic dishwasher compositions of this invention are readily employed in known manner for washing dishes, other kitchen utensils and the like in an automatic dishwasher, provided with a suitable detergent dispenser, in an aqueous wash bath cont~in;ng an effective amount of the composition, generally sufficient to fill or partially fill the automatic dispenser cup of the particular machine being used.
The invention also provides a method for cleaning dishware in an automatic dishwashing machine with an aqueous wash bath cont~; n; ng an effective amount of the liquid linear viscoelastic automatic dishwasher detergent composition as described above. The composition can be readily poured from the polyethylene cont~;ner with little or no squeezing or shaking into the dispensing cup of the automatic dishwashing machine and will be sufficiently viscous and cohesive to remain securely within the dispensing cup until shear forces - 20~1~18 are again applied thereto, such as by the water spray from the dishwashing machine.
The invention may be put into practice in various ways and a number of specific emhodimpnts will be described to illustrate the invention with reference to the accompanying examples. I
All the amounts and proportions referred to herein are by weight of the composition unless otherwise indicated.

Example 1 The following formulations A-K were prepared as described below:

INr~nTR~T ¦ A B C D E F G H I J K
/FORMULATION
DEIONIZED WATER BAL. BAL. BAL. BAL. BAL. BAL. BAL. BAL. BAL. BAL. BAL.
CARBOPOL 941 0.9 0.9 0.9 0.9 1 --- 0.9 0.9 --- 1.5 0.9 NaOH (50%) 2.4 2.4 2.4 2.4 3.5 3.5 2.4 --- 2.4 2.4 2.4 KOH (50%) --- --- --- --- --- --- --- 2.4 --- --- ---TPP 13 13 12 7.5 7.5 7.5 --- --- 13 7.5 13 HEXAHYDRATE, Na Na SILICATE 21 21 21 21 17 17 21 --- 21 21 21(47.5%)(1:2.3) (29.1%)(1:2.3) ~p LPKN (5%) 3.2 3.2 3.2 3.2 --- --- 3.2 3.2 3.2 3.2 3.2 FATTY ACID2 0.1 0.1 0.1 0.1 --- --- 0.1 0.1 1 0.1 0.1 BLEACH (13.0% 7.5 7.5 7.5 7.5 9.1 9.1 7.5 7.5 7.5 7.5 9 CL) AIR3 Vol.~) <2.0 <2.0 <2.0 <2.0 <2.0 >2.0 <2.0 ~2.0 >2.0 <2.0 <2.0 FRAGRANCE --- 0.17 --- --- --- --- --- --- --- --- ---K/Na RATIO 1.12 1.12 1.16 1.89 1.95 1.95 4.16 45.15 --- 1.89 ---lo q / 't l ~

--a~ ,~
In C E ~d r ~ O ~
o o , ,,~ . . ~ OS
~ :4 o o _ c~
O R ~~
o O 0 H 1 14 ~ ~ r --- _ a; ~
~D O O a . . . S
I~ o o ~;
I.,~ ~ ~ ~L
~ I ~ ~

_ ~ o _ V ,~ ~4 o ~ o~
~ 1 s~
o o ~ 1 C
~ ~ ~ 1 td-~l I o o I
I ~ ~ ~- ~ o ~1 1) _ o o ~~ a~
~ o o ~ o _ .c a~
~ ~~ o r ~ E a~
~~ o o ~1 . ~,1 ~ ~ ~ , o a ~ ~4 0 0 _ ~ ~ ~.C' R~
u~ . ~ L o O O ~ P ~D
~ ~:4 0 ~ ' _ c O
1 o o o uo_ ~~
' ' ' a~ r 1~~ o o 4 o ~
1~ U 1) 3 r o o ~ C ~0 _, ~4 0 0 ., ~a s 1) O ~ Ll ~ _ _~ rr er ~ S~ O
O f a~ ~\ 0 41 >
O L ~ ~ 4/
tr ~ . ~ ~ ,,u, Z ~ ~ ~no3 ~ u~o--~0 ~ ~oO~o ~ ~ u~ co u ~ ~--_ 2091~18 Formulations A, B, C, D, E, G, J, and K are prepared by ~first forming a uniform dispersion of the Carbopol 941 or 940 thickener in about 97% of the water (balance). The Carbopol is slowly added to deionized water at room temperature using a mixer equipped with a premier blade, with agitation set at a medium shear rate, as reco~ en~ed by the manufacturer. The dispersion is then neutralized by addition, under mixing, of the caustic soda (50% NaOH or KOH) component to form a thickened product of gel-like consistency.
To the resulting gelled dispersion the silicate, tetrapotassium pyrophosphate (TKPP), sodium tripolyphosphate TP(TPP, Na) and bleach, are added sequentially, in the order stated, with the mixing continued at medium shear.
Separately, an emulsion of the phosphate anti-foaming agent (LPKN), stearic acidlpalmitic acid mixture and detergent (Dowfax 3B2) is prepared by adding these ingredients to the re~;n;ng 3% of water (balance) and heating the resulting mixture to a temperature in the range of 50~C to 70~C.
This heated emulsion is then added to the previously prepared gelled dispersion under low shear conditions, such that a vortex is not formed.
The rem~;n;ng formulations F, H and I are prepared in essentially the same manner as described above except that the heated emulsion of LPKN, stearic acid and Dowfax 3B2 is directly added to the neutralized Carbopol dispersion prior to the addition of the r~m~;n;ng ingredients. As a result, formulations F, H and I, have higher levels of incorporated air and densities below 1.30 g/cc.

- - - -- - ~ -. _ 2 o~

The rheograms for the formulations A, C, D, G and J are shown in figures 1-5, respectively, and rheograms for formulations H, I and K are shown in figures 6, 7 and 8 respectively.
These rheograms are obtained with the System 4 Rheometer from Rheometrics equipped with a Fluid Servo with a 100 grams-centimeter torque transducer and a 50 millimeter parallel plate geometry having an 0.8 millimeter gap between plates.
All measurements are made at room temperature (25~C+1~C) in a humidity chamber after a 5 minute or 10 minute holding period of the sample in the gap. The measurements are made by applying a frequency of 10 radians per second.
All of the composition formulations A, B, C, D, G and J
according to the preferred embo~;m~t of the invention which include Carbopol 941 and stearic acid exhibit linear viscoelasticity as seen from the rheograms of figure 1-5.
Formulation E which includes Carbopol 941 but not stearic acid showed no phase separation at either room temperature or 100~F
after 3 weeks, but exhibited 10% phase separation after 8 weeks at room temperature and after only 6 weeks at 100~F.
Formulation K, containing Carbopol 940 in place of Carbopol 941, as seen from the rheogram in figure 8, exhibits substantial linearity over the strain range of from 2% to 50%
(G' at 1% strain-G' at 50% strain 500 dynes/sq.cm.) although tan 1 at a strain above 50%.

,.- 2~3l~l8 ~xample 2 This example demonstrates the importance of the order of addition of the surface active component premix to the rP~;n~er of the composition on product density and stability.
The following formulations are prepared by methods A and B:
Ingredient Water, deionized Balance Carbopol 941 0.5 NaOH (50%) 2.4 Na Silicate (47.5%) 21 TPP, Na 13 Bleach (1%) 7.5 LPKN 0.16 Stearic Acid 0.1 Dowfax 3B2 Method A:
The Carbopol 941 is dispersed, under medium shear rate, using a premier blade mixer, in deionized water at ambient temperature. The NaOH is added, under mixing, to neutralize and gel the Carbopol 941 dispersion. To the thickened mixture the following ingredients are added sequentially while the stirring is continued: sodium silicate, TKPP, TPP, and bleach.
Separately, an emulsion is prepared by adding the Dowfax 3B2, stearic acid and LPgN to water while mixing at moderate shear and heating the mixture to about 65~C to finely disperse the emulsified surface active ingredients in the water phase.
This emulsion premix is then slowly added to the Carbopol dispersion while mixing under low shear conditions without forming a vortex. The results are shown below.

2091~1~

_ Method B:
Method A is repeated except that the heated emulsion premix is added to the neutralized Carbopol 941 dispersion before the sodium stearate, TKPP, TPP, and bleach. The results are also shown below.
Method A Method B
Density (glcc) 1.38 1.30 Stability (RT-8 weeks)0.00% 7.00%
Rheogram Fig. 9 Fig.10 From the rheograms of figures 9 and 10 it is seen that both products are linear viscoelastic although the elastic and viscous moduli G' and G" are higher for Method A than for Method B.
From the results it is seen that early addition of the surface active ingredients to the Carbopol gel significantly increases the degree of aeration and lowers the bulk density of the final product. Since the bulk density is lower than the density of the continuous liquid phase, the liquid phase undergoes inverse separation (a clear liquid phase forms on the bottom of the composition). This process of inverse separation appears to be kinetically controlled and will occur faster as the density of the product becomes lower.

Example 3 This example shows the importance of the temperature at ~ which the premixed surfactant emulsion is prepared.
Two formulations, L and M, having the same composition as in Example 2 except that the amount of stearic acid was increased from 0.1% to 0.2% are prepared as shown in Method A

2091~18 .
for formulation L and by the following Method C for formulation M.

Method C
The procedure of Method A is repeated in all details except that emulsion premix of the surface active ingredients is prepared at room temperature and is not heated before being post-added to the thickened Carbopol dispersion cont~i n; ng silicate, builders and bleach. The rheograms for formulations L and M are shown in figures 11 and 12, respectively. From these rheograms it is seen that formulation L is linear viscoelastic in both G' and G" whereas formulation M is non-linear viscoelastic particularly for elastic modulus G' (G' at 1% strain-G' at 30% strain > 500 dynes/cm2) and also for G"
(G" at 1% strain-G" at 30% strain ~ 300 dynes/cmZ).
Formulation L re~; n.~ stable after storage at RT and 100~F for at least 6 weeks whereas formulation M undergoes phase separation.
C~mrArative Example 1 The following formulation is prepared without any potassium salts:
Weight %
Water Balance Carbopol 941 0.2 NaOH (50%) 2.4 TPP, Na (50%) 21.0 Na Silicate (47.5%) 17.24 Bleach (1%) 7.13 Stearic Acid 0.1 LPKN (5%) 3.2 Dowfax 3B2 0.8 Soda Ash 5.0 Acrysol LMW 45-N 2.0 - 2(~91~18 .
The procedure used is analogous to Method A of Example 2 with the soda ash and Acrysol LMW 45-N (low molecular weight polyacrylate polymer) being added before and after, respectively, the silicate, TPP and bleach, to the thickened Carbopol 941 dispersion, followed by addition to the heated surface active emulsion premix. The rheogram is shown in figure 13 and is non~ eAr with G"/G' (tan ) > 1 over the range of strain of from about 5% to 80%.

Example 4 Formulations A, B, C, D and K according to this invention and comparative formulations F and a commercial liquid automatic dishwasher detergent product as shown in Table 1 above were subjected to a bottle residue test using a stAn~rd polyethylene 28 ounce bottle as used for current commercial liquid dishwasher detergent bottle.
Six bottles are filled with the respective samples and the product is dispensed, with a min;mllm of force, in 80 gram dosages, with a 2 minute rest period between dosages, until flow stops. At this point, the bottle was vigorously shaken to try to expel additional product.
The amount of product remAining in the bottle is measured as a percentage of the total product originally filled in the bottle. The results are shown below.

2091~18 ~ Bottle Residue Formulation Residue C

F*
Co~rcial Product 20 ~The sample separates upon aging.

Claims (12)

1. A viscoelastic aqueous liquid automatic dishwasher detergent composition comprising approximately by weight:
(a) 10 to 35% of at least one alkali metal detergent builder salt, said alkali metal detergent builder salt being selected from the group consisting essentially of alkali metal tripolyphosphate, alkali metal pyrophosphate, alkali metal metaphosphate, alkali metal carbonate, alkali metal citrate and alkali metal nitrilotriacetate and mixtures thereof;
(b) 0 to 25% alkali metal silicate;
(c) 0 to 6% alkali metal hydroxide;
(d) 0 to 5.0% chlorine bleach stable, water-dispersible, organic detergent active material;
(e) 0 to 1.5% chlorine bleach stable foam depressant;
(f) chlorine bleach compound in an amount to provide 0.2 to 4% of available chlorine;
(g) 0.1 to 2.0% of at least one cross-linked polyacrylic acid thickening agent having a molecular weight of from about 500,000 to 10,000,000;
(h) 0 to 2% of a long chain fatty acid or a metal salt of a fatty acid;
(i) 0 to 15% of a non-cross-linked polyacrylate having a molecular weight of about 1,000 to 100,000; and (j) water, wherein said polyacrylic acid thickening agent being selected from the group consisting essentially of acrylic acid or methacrylic acid, water-dispersible or water-soluble salts, esters, or amides thereof, and water-soluble copolymers of these acids or their salts, ester, or amides with each other or with one or more other ethylenically unsaturated monomers, wherein the aqueous phase includes both sodium and potassium ions at a K/Na weight ratio of from about 1:1 to about 1:30, wherein substantially all of the normally solid components of the composition are present dissolved in the aqueous phase, and substantially all of the water in the composition is tightly bound to the cross-linked polyacrylic acid thickening agent, said composition having a bulk density of from 1.26 g/cm3 to 1.42 g/cm3 and said composition does not exhibit phase separation and remains homogenous, when said composition is centrifuged at 1000 rpm for 30 minutes.

2. The composition of Claim 1, wherein said alkali metal builder salt is a mixture of sodium tripolyphosphate and potassium tripolyphosphate.

3. The composition of Claim 1, wherein said alkali metal builder salt is a mixture of sodium tripolyphosphate and potassium pyrophosphate.

4. The composition of Claim 1 wherein said alkali metal builder salt is a mixture of sodium tripolyphosphate, potassium tripolyphosphate, and potassium pyrophosphate and mixture thereof.

5. The composition of Claim 1, wherein the long chain fatty acid is stearic acid.

6. The composition of Claim 1 which further comprises up to about 2% by volume, based on the total volume of the composition, of air in the form of finely dispersed bubbles.

7. The composition of Claim 1 wherein the cross-linked polyacrylic acid thickening is present in an amount of from about 0.4 to 1.5% by weight of the composition.

8. The composition of Claim 1 wherein the K/Na ratio is from about 1:1 to about 1:20.

9. The composition of Claim 1 which the chlorine bleach compound is sodium hypochlorite.

10. The composition of Claim 1 further including a fragrance.

11. The composition of Claim 1 further including a dyestuff or pigment.

12. The composition of Claim 1 further including a dyestuff or pigment.