Technical Field
[0001] The present invention relates to detergent compositions containing organic surfactant,
non-phosphate detergent builder, preferably an alkali metal silicate, and polyacrylate
polymer having a weight average molecular weight of from about 2,000 to about 10,000.
Background Art
[0002] U.S. Patent 4,072,621, Rose, issued Feb. 7, 1978, discloses the addition of a water-soluble
copolymer of a vinyl compound and maleic anhydride to granular detergents containing
aluminosilicate builders.
[0003] British Patent 2,048,841, Burzlo, published Dec. 17, 1980, discloses the use of polymeric
acrylamides to stabilize aqueous suspensions of zeolites. The suspensions are said
to be suitable for spray-drying to obtain detergent compositions.
[0004] U.S. Patent 3,933,673, Davies, issued Jan. 20, 1976, describes the use of partial
alkali metal salts of homo- or copolymers of unsaturated aliphatic mono- or polycarboxylic
acids as builders which provide improved storage properties.
[0005] U.S. Patent 3,794,605, Diehl, issued Feb. 26, 1974, relates to the use of from 0.1%
to 20% of a mixture of salts of cellulose sulfate esters and copolymers of a vinyl
compound with maleic anhydride to provide whiteness maintenance benefits to detergent
compositions.
[0006] U.S. Patent 3,922,230, Lamberti et al, issued November 25, 1975, discloses detergent
compositions containing oligomeric polyacrylates.
[0007] U.S. Patent 4,031,022, Vogt et al, issued June 21, 1977, discloses detergent compositions
containing copolymers of alpha- hydroxyacrylic acid and acrylic acid.
[0008] U.S. Patent 4,378,080, Murphy, issued April 5, 1983, discloses low levels of film
forming polymers for improving detergent granules' structure.
[0009] British Patent Application 2,097,419A, published November 3, 1982, discloses "base
bead" compositions containing low levels of low molecular weight especially 1,000-2,000,
polyacrylate for structure reasons.
[0010] British Patent 1,333,915, published Oct. 17, 1973, discloses that polyacrylic acids
of molecular weight greater than 1000 and having from 5-55% of its carboxyl groups
neutralized as the sodium salt are free-flowing powders useful as detergent builders.
[0011] British Patent 1,380,402, Pritchard et al, published Jan. 15, 1975, relates to the
addition of low levels of reactive and nonreactive polymers to provide free-flowing
granular detergents containing nonionic surfactants.
Summary of the Invention
[0012] The present invention encompasses a detergent composition comprising:
(a) from about 5% to about 50% by weight of organic surfactant selected from the group
consisting of anionic, nonionic, zwitterionic, ampholytic and cationic surfactants,
and mixtures thereof;
(b) from about 5% to about 80% by weight of non-phosphorous detergent builder;
(c) from about 0.3% to about 5% by weight of a polyacrylate polymer soluble in an
aqueous slurry comprising the above components and having a weight average molecular
weight of from about 2,000 to about 10,000.
Detailed Description of the Invention
[0013] The detergent compositions of the present invention contain organic surfactant, water-soluble
non-phosphorus detergent builder, and a polyacrylate polymer of selected molecular
weight at a low level. The polyacrylate polymers herein provide a surprising boost
to the removal of clay soils even at these low levels which do not provide substantial
builder capacity.
[0014] The compositions of the present invention can be prepared by drying an aqueous slurry
comprising the components, by agglomeration or by mixing the various ingredients,
either dry or in liquid form, either aqueous or anhydrous. The effect is obtained
regardless of the method of preparation. It is believed that the effect is obtained
by some kind of surface modification.
Organic Surfactant
[0015] The detergent compositions herein contain from about 5% to about 50% by weight of
an organic surfactant selected from the group consisting of anionic, nonionic, zwitterionic,
ampholytic and cationic surfactants, and mixtures thereof. The surfactant preferably
represents from about 10% to about 30% by weight of the detergent composition. Surfactants
useful herein are listed in U.S. Patent 3,664,961, Norris, issued May 23, 1972, and
in U.S. Patent 3,919,678, Laughlin, et al, issued December 30, 1975, both incorporated
herein by reference. Useful cationic surfactants also include those described in U.S.
Patent 4,222,905, Cockrell, issued September 16, 1980, and in U.S. Patent 4,239,659,
Murphy, issued December 16, 1980, both incorporated herein by reference.
[0016] Water-soluble salts of the higher fatty acids, i.e.. "soaps", are useful anionic
surfactants in the compositions herein. This includes alkali metal soaps such as the
sodium, potassium, ammonium, and substituted ammonium salts of higher fatty acids
containing from about 8 to about 24 carbon atoms, and preferably from about 12 to
about 18 carbon atoms. Soaps can be made by direct saponification of fats and oils
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.
[0017] Useful anionic surfactants also include the water-soluble salts, preferably the alkali
metal, ammonium and substituted ammonium salts, of organic sulfuric reaction products
having in their molecular structure an alkyl group containing 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 this group of synthetic
surfactants are the sodium and potassium alkyl sulfates, especially those obtained
by sulfating the higher alcohols (CB-C18 carbon atoms) . such as those produced by
reducing the glycerides of tallow or coconut oil; and the sodium and potassium alkylbenzene
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. Patents 2,220,099 and 2,477,383. Especially valuable are linear straight chain
alkylbenzene sulfonates in which the average number of carbon atoms in the alkyl group
is from about 11 to 13, abbreviated as C11-nLAS.
[0018] Other anionic surfactants herein are the sodium alkyl glyceryl ether sulfonates,
especially those ethers of higher alcohols derived from tallow and coconut oil; sodium
coconut oil fatty acid monoglyceride sulfonates and sulfates; sodium or potassium
salts of alkyl phenol ethylene oxide ether sulfates containing from about 1 to about
10 units of ethylene oxide per molecule and from about 8 to about 12 carbon atoms
in the alkyl group; and sodium or potassium salts of alkyl ethylene oxide ether sulfates
containing about 1 to about 10 units of ethylene oxide per molecule and from about
10 to about 20 carbon atoms in the alkyl group.
[0019] Other useful anionic surfactants include the water-soluble salts of esters of alpha-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 olefin sulfonates containing from about 12 to 24 carbon
atoms; and beta-alkyloxy alkane sulfonates containing from about 1 to 3 carbon atoms
in the alkyl group and from about 8 to 20 carbon atoms in the alkane moiety.
[0020] Water-soluble nonionic surfactants are also useful in the compositions of the invention.
Such nonionic materials include 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.
[0021] Suitable nonionic surfactants include the polyethylene oxide condensates of alkyl
phenols, e.g., the condensation products of alkyl phenols having an alkyl group containing
from about 6 to 15 carbon atoms, in either a straight chain or branched chain configuration,
with from about 3 to 12 moles of ethylene oxide per mole of alkyl phenol.
[0022] Preferred nonionics are the water-soluble condensation products of aliphatic alcohols
containing from 8 to 22 carbon atoms, in either straight chain or branched configuration,
with from 3 to 12 moles of ethylene oxide per mole of alcohol. Particularly preferred
are the condensation products of alcohols having an alkyl group containing from about
9 to 15 carbon atoms with from about 4 to 8 moles of ethylene oxide per mole of alcohol.
[0023] Semi-polar nonionic surfactants useful herein include water-soluble amine oxides
containing one alkyl moiety of from about 10 to 18 carbon atoms and two moieties selected
from the group consisting of alkyl groups and hydroxyalkyl groups containing from
1 to 3 carbon atoms; water-soluble phosphine oxides containing one alkyl moiety of
about 10 to 18 carbon atoms and two moieties selected from the group consisting of
alkyl groups and hydroxyalkyl groups containing from about 1 to 3 carbon atoms; and
water-soluble sulfoxides containing one alkyl moiety of from about 10 to 18 carbon
atoms and a moiety selected from the group consisting of alkyl and hydroxyalkyl moieties
of from about 1 to 3 carbon atoms.
[0024] Ampholytic surfactants include derivatives of aliphatic or aliphatic derivatives
of heterocyclic secondary and tertiary amines in which the aliphatic moiety can be
straight chain or branched and wherein one of the aliphatic substituents contains
from about 8 to 18 carbon atoms and at least one aliphatic substituent contains an
anionic water-solubilizing group.
[0025] Zwitterionic surfactants include derivatives of aliphatic quaternary ammonium, phosphonium,
and sulfonium compounds in which one of the aliphatic substituents contains from about
8 to 18 carbon atoms.
[0026] Particularly preferred surfactants herein do not comprise substantial amounts of
nonionic detergent surfactants and, preferably, are anionic surfactants, especially
those selected from the group consisting of the alkali metal salts of C
11-13 alkylbenzene sulfonates, C
14-18 alkyl sulfates, C
14-18 alkyl linear polyethoxy sulfates containing from about 1 to about 4 moles of ethylene
oxide, and mixtures thereof.
The Non-Phosphorous Detergent Builder
[0027] The compositions of the present invention also contain from about 5% to about 80%,
preferably from about 10% to about 70%, and most preferably from about 15% to about
60%, by weight of a non-phosphorous detergent builder. The non-phosphorous detergent
builder can be either organic or inorganic in nature. They function as detergency
builder materials in the laundering solution.
[0028] Non-phosphorous detergent builder are generally selected from the various water-soluble,
alkali metal, ammonium or substituted ammonium carbonates, silicates, carboxylates,
and polycarboxylates other than the polyacrylates as defined hereinafter, especially
non-polymeric polycarboxylates. Preferred are the alkali metal, especially sodium,
salts of the above. However, the present compositions preferably contain less than
about 6%, more preferably less than about 4%, by weight of silicate materials for
optimum granule solubility.
[0029] Specific examples of non-phosphorus, inorganic builders are sodium and potassium
carbonate, bicarbonate, sesquicarbonate, tetraborate decahydrate, and silicate having
a molar ratio of Si0
2 to alkali metal oxide of from about 0.5 to about 4.0, preferably from about 1.0 to
about 2.4.
[0030] An especially preferred detergency builder is crystalline aluminosilicate ion exchange
material of the formula

wherein z and y are at least about 6, the molar ratio of z to y is from about 1.0
to about 0.5 and x is from about 10 to about 264. Amorphous hydrated aluminosilicate
materials useful herein have the empirical formula

wherein M is sodium, potassium, ammonium or substituted ammonium, z is from about
0.5 to about 2 and y is 1, said material having a magnesium ion exchange capacity
of at least about 50 milligram equivalents of CaC0
3 hardness per gram of anhydrous aluminosilicate.
[0031] The aluminosilicate ion exchange builder materials herein are in hydrated form and
contain from about 10% to about 28% of water by weight if crystalline, and potentially
even higher amounts of water if amorphous. Highly preferred crystalline aluminosilicate
ion exchange materials contain from about 18% to about 22% water in their crystal
matrix. The crystalline aluminosilicate ion exchange materials are further characterized
by a particle size diameter of from about 0.1 micron to about 10 microns. Amorphous
materials are often smaller, e.g., down to less than about 0.01 micron. Preferred
ion exchange materials have a particle size diameter of from about 0.2 micron to about
4 microns. The term "particle size diameter" herein represents the average particle
size diameter of a given ion exchange material as determined by conventional analytical
techniques such as, for example, microscopic determination utilizing a scanning electron
microscope. The crystalline aluminosilicate ion exchange materials herein are usually
further characterized by their calcium ion exchange capacity, which is at least about
200 mg. equivalent of CaC0
3 water hardness/g. of aluminosilicate, calculated on an anhydrous basis, and which
generally is in the range of from about 300 mg. eq./g. to about 352 mg. eq./g. The
aluminosilicate ion exchange materials herein are still further characterized by their
calcium ion exchange rate which is at least about 2 grains Ca
++/gallon/minutelgram/gallon of aluminosilicate (anhydrous basis), and generally lies
within the range of from about 2 grains/gallon/minute/gram/gallon to about 6 grains/gallon/minute/gram/gallon,
based on calcium ion hardness. Optimum aluminosilicate for builder purposes exhibit
a calcium ion exchange rate of at least about 4 grains/gallon/minute/gram/gallon.
[0032] The amorphous aluminosilicate ion exchange materials usually have a Mg exchange capacity
of at least about 50 mg. eq. CaC0
3/g. (12 mg. Mg
++/g.) and a Mg
++ exchange rate of at least about 1 grain/gallon/minute/gram/gallon. Amorphous materials
do not exhibit an observable diffraction pattern when examined by Cu radiation (1.54
Angstrom Units).
[0033] Aluminosilicate ion exchange materials useful in the practice of this invention are
commercially available. The aluminosilicates useful in this invention can be crystalline
or amorphous in structure and can be naturally-occurring aluminosilicates or synthetically
derived. A method for producing aluminosilicate ion exchange materials is discussed
in U.S. Patent 3,985,669, Krummel et al, issued October 12, 1976, incorporated herein
by reference. Preferred synthetic crystalline aluminosilicate ion exchange materials
useful herein are available under the designations Zeolite A, Zeolite B, and Zeolite
X. In an especially preferred embodiment, the crystalline aluminosilicate ion exchange
material in Zeolite A and has the formula

wherein x is from about 20 to about 30, especially about 27.
[0034] Water-soluble, non-phosphorus organic builders useful herein include the various
alkali metal, ammonium and substituted ammonium, carboxylates, polycarboxylates and
polyhydroxysulfon- ates. Examples of non-polymeric polycarboxylate builders are the
sodium, potassium, lithium, ammonium and substituted ammonium salts of ethylenediaminetetraacetic
acid, nitrilotriacetic acid, oxydisuccinic acid, mellitic acid, benzene polycarboxylic
acids, and citric acid. The compositions of this invention only contain the limited
amount of polyacrylate defined hereinafter.
[0035] Other useful builders herein are sodium and potassium carboxymethyloxymalonate, carboxymethyloxysuccinate,
cis-cyclo- hexanehexacarboxylate, cis-cyclopentanetetracarboxylate, and phloroglucinol
trisulfonate.
[0036] Other suitable polycarboxylates are the polyacetal carboxylates described in U.S.
Patent 4,144,226, issued March 13, 1979 to Crutchfield, et al., and U.S. Patent 4,246,495,
issued March 27, 1979 to Crutchfield, et al., both incorporated herein by reference.
These polyacetal carboxylates can be prepared by bringing together under polymerization
conditions an ester of glyoxylic acid and a polymerization initiator. The resulting
polyacetal carboxylate ester is then attached to chemically stable end groups to stabilize
the polyacetal carboxylate against rapid depolymerization in alkaline solution, converted
to the corresponding salt, and added to a surfactant.
[0037] Other detergency builder materials useful herein are the "seeded builder" compositions
disclosed in Belgian Patent No. 798,856, issued October 29, 1973, incorporated herein
by reference. Specific examples of such seeded builder mixtures are: 3:1 wt. mixtures
of sodium carbonate and calcium carbonate having 5 micron particle diameter; 2.7:1
wt. mixtures of sodium sesquicarbonate and calcium carbonate having a particle diameter
of 0.5 microns; 20:1 wt. mixtures of sodium sesquicarbonate and calcium hydroxide
having a particle diameter of 0.01 micron; and a 3:3:1 wt. mixture of sodium carbonate,
sodium aluminate and calcium oxide having a particle diameter of 5 microns.
[0038] Preferably the builder is selected from the group consisting of zeolites, especially
Zeolite A; carbonates, especially sodium carbonate; and citrates, especially sodium
citrate.
[0039] Soaps, as described hereinbefore, can also act as builders depending upon the pH
of the wash solution, the insolubility of the calcium and/or magnesium soaps, and
the presence of other builders and soap dispersants.
[0040] The compositions herein preferably contain from about 0% to about 6%, preferably
from about 0.5% to about 5%, and most preferably from about 1% to about 4%, by weight
of an alkali metal silicate having a molar ratio of Si0
2 to alkali metal oxide of from about 1.0 to about 3.2, preferably from about 1.6 to
about 2.4. Sodium silicate, particularly one having a molar ratio of from about 1.8
to about 2.2, is preferred.
[0041] The alkali metal silicates can be purchased in either liquid or granular form. Silicate
slurries can conveniently be used to avoid having to dissolve the dried form in the
aqueous slurry (e.g., crutcher mix) of the components herein.
Polyacrylate Polymer
[0042] The compositions of the present invention contain from about 0.3% to about 5%, preferably
from about 1.0% to about 3%, and more preferably from about 1.5% to about 2%, by weight
of a polyacrylate polymer having a molecular weight of from about 2,000 to about 10,000,
preferably from about 3,000 to about 8,000, and more preferably from about 3,000 to
about 6,000. Optimum solubility of the polymer is obtained when it is in the form
of an at least partially neutralized alkali metal, ammonium or substituted ammonium
(e.g., mono-, di- or triethanol ammonium) salt. The alkali metal, especially sodium,
salts are most preferred.
[0043] Lower levels of polyacrylate are preferred for cost reasons and there is less chance
of an adverse effect on other detergent properties, e.g., cleaning of other soils,
performance by minor ingredients such as enzymes or brighteners, etc.
[0044] Suitable polymers herein are the at least partially neutralized salts of polymers
of acrylic acid. One can also use copolymers formed with small amounts of other copolymerisable
monomers. The percentage by weight of the polymer units which is derived from acrylic
acid is preferably greater than about 80%. Suitable . copolymerisable monomers include,
for example, methacrylic acid, hydroxyacrylic acid, vinyl chloride, vinyl alcohol,
furan, acrylonitrile, methacrylonitile, vinyl acetate, methyl acrylate, methyl methacrylate,
styrene, alpha-methylstyrene, vinyl methyl ether, vinyl ethyl ether, vinyl propyl
ether, acrylamide, ethylene, propylene and 3-butenoic acid.
[0045] Preferred copolymers of the above group contain at least about 90% by weight of units
derived from the acrylic acid. Preferably essentially all of the polymer is derived
from acrylic acid. Particularly preferred is sodium polyacrylate, especially when
it has an average molecular weight of from about 3,000 to about 6,000.
Optional Components
[0046] The compositions of the invention preferably contain from about 0.3% to about 6.0%,
preferably from about 0.5% to about 4.0%, and more preferably from about 0.7% to about
3.0% by weight of a water-soluble polymeric material, or mixtures thereof, containing
at least about 50% ethylene oxide by weight, said polymer or mixtures thereof having
a melting point not less than about 35°C. Preferably the polymeric material will have
a melting point not less than about 45°C, more preferably not less than about 50°C
and most preferably not less than about 55°C. Because the polymeric materials useful
in the practice of the invention are generally mixtures representing a range of molecular
weights, the materials tend to soften and begin to become liquid over a range of temperatures
of from about 3°C to about 7°C above their melting point. Mixtures of two or more
polymeric materials can have an even wider range.
[0047] Preferred polymers contain at least about 70% ethylene oxide by weight and more preferred
polymers contain at least about 80% ethylene oxide by weight. Polyethylene glycol
which can be said to contain essentially 100% ethylene oxide by weight is particularly
preferred.
[0048] Preferred polyethylene glycols have an average molecular weight at least about 1000,
and more preferably from about 2500 . to about 20,000 and most preferably from about
3000 to about 10,000.
[0049] Other suitable polymeric materials are the condensation products of C
10-20 alcohols or C
8-18 alkyl phenols with sufficient ethylene oxide, not less than about 50% by weight of
the polymer, so that the resultant product has a melting point above about 35°C.
[0050] Block and heteric polymers based on ethylene oxide and propylene oxide addition to
a low molecular weight organic compound containing one or more active hydrogen atoms
are suitable in the practice of the invention. Polymers based on the addition of ethylene
oxide and propylene oxide to propylene glycol, ethylenediamine, and trimethylolpropane
are commercially available under the names Pluronicso, Pluronicø R, Tetronicsa and
Pluradots® from the BASF Wyandotte Corporation of Wyandotte, Michigan. Corresponding
nonproprietary names of the first three trade names are poloxamer, meroxapol and poloxamine,
respectively.
[0051] Preferably these ethylene oxide polymers are incorporated into the detergent crutcher
and dried with a major portion of the detergent composition when forming granular
compositions.
[0052] Other ingredients commonly used in detergent compositions can be included in the
compositions of the present invention. These include solvents, diluents, sources of
ionic strength, color speckles, bleaching agents and bleach activators, suds boosters
or suds suppressors, anti-tarnish and anti-corrosion agents, soil release agents,
dyes, fillers, optical brighteners, germicides, non-builder alkalinity sources, enzymes,
enzyme-stabilizing agents, and perfumes.
[0053] The following non-limiting examples illustrate the detergent compositions of the
present invention.
[0054] All percentages, parts, and ratios used herein are by weight unless otherwise specified.
EXAMPLE I
[0055]

[0056] The above compositions with the indicated amounts of the indicated sodium polyacrylates
were tested in automatic miniwashers with assorted soils and stains present including
the particulate soil (clay) that defines the "Cleaning Index". The "Cleaning Index"
is obtained by finding the panel score grades for each product using a scale in which
0 means "There is no difference."; 1 means "I think I see a difference."; 2 means
"I see a difference."; and 3 means "I see a big difference.". The control product
contains no polyacrylate and the best performing product is set at 100 with all other
grades being ranked as a percent of the difference.
Test 1
[0057] Conditions: 95°F; indicated water hardness; Product A with different molecular weight
sodium polyacrylates at the 1.5% level.

Test 2
[0058] Conditions: 95°F, indicated hardness, Product B with 1.5% of sodium polyacrylate
with the indicated molecular weight.

[0059] As can be seen from the above, there is essentially no benefit from using a polyacrylate
with a molecular weight above about 10,000 and for a consistent meaningful benefit,
the molecular weight should be less than about 8,000. For optimum performance, the
molecular weight should not exceed about 6,000. Polymers containing less than 100%,
e.g., 80%, acrylate monomers can be used with substantially equivalent results.
Test 3
[0060] Conditions: 95°F; underbuilt, and Product A containing the indicated amounts of Na
Zeolite A and Na Polyacrylate (M.W. 4500).

[0061] As can be seen from the above, the clay improvement is essentially independent of
the amount of other detergent builder present and there is essentially no advantage
in using more than about 5% of the polyacrylate.
EXAMPLE II
[0062]

[0063] The above composition was prepared as a spray-dried granule and tested with (control)
and without 1.5% added sodium polyacrylate (M.W. 4500). The temperature was 95°F.,
the water had 10 grains/gal. hardness and the results in panel score grade units difference
were as follows for clay removal.
[0064] Clay on cotton fabric: 0.9 LSD = 0.51
[0065] Clay on polycotton fabric: 1.0 LSD = 0.41
[0066] Based on these results, it is clear that a small amount of a low molecular weight
polyacrylate provides a substantial cleaning boost for clay removal.
[0067] Preferred compositions are (1) spray-dried detergent granules wherein at least the
surfactant and, preferably, the detergent builder are both in the detergent crutcher
mix prior to spray drying and (2) liquid compositions.
1. A detergent composition comprising:
(a) from about 5% to about 50% by weight of an organic detergent surfactant selected
from the group consisting of anionic, nonionic, zwitterionic, ampholytic and cationic
surfactants, and mixtures thereof;
(b) from about 5% to about 80% by weight of a non-phosphorus detergent builder;
(c) from about 0.3% to about 5% by weight of a polyacrylate polymer soluble in an
aqueous slurry comprising the above components and having a weight average molecular
weight of from about 2,000 to about 10,000.
2. The composition of Claim 1 wherein the organic surfactant comprises an anionic
surfactant selected from the group consisting of alkali metal salts of C11-13 alkylbenzene sulfonates, C14-18 alkyl sulfates, C14-18 alkyl polyethoxy sulfates containing from about 1 to about 4 moles of ethy!ene oxide,
and mixtures thereof.
3. The composition of Claim 1 wherein the non-phosphate detergent builder comprises
a zeolite, a carbonate or mixtures thereof.
4. The composition of Claim 1 comprising from about 1% to about 4% by weight of an
alkali metal silicate having a molar ratio of from about 1.6 to about 2.4.
5. The composition of Claim 1 wherein the polyacrylate is a salt of a homopolymer
of acrylic acid, hydroxyacrylic acid or methacrylic acid, or a copolymer thereof containing
at least about 80% by weight of units derived from said acids.
6. The composition of Claim 5 wherein the polymer has a weight average molecular weight
of from about 3,000 to about 6,000.
7. The composition of Claim 6 wherein the polymer is sodium polyacrylate.
8. The composition of Claim 2 comprising from about 10% to about 30% by weight of
the organic surfactant; from about 15% to about 60% by weight of non-phosphate detergent
builder salt comprising hydrated sodium Zeolite A, carbonate, nitrilotriacetate, or
mixtures thereof.
9. The composition of Claim 8 comprising from about 1% to about 3% by weight of sodium
polyacrylate having a weight average molecular weight of from about 3,000 to about
8,000.
10. The composition of Claim 9 prepared by spray-drying an aqueous slurry of the components.
11. The composition of Claim 10 comprising from about 10% to about 30% by weight of
aluminosilicate ion exchange material of the formula Na12[[AlO2)12.(SiO2)12].x H20, wherein x is from about 20 to about 30.
12. The composition of Claim 1 which is substantially free of nonionic detergent surfactant.
13. The composition of Claim 12 wherein the non-phosphate detergent builder comprises
a zeolite, a carbonate or mixtures thereof.
14. The composition of Claim 12 comprising from about 1% to about 4% by weight of
an alkali metal silicate having a molar ratio of from about 1.6 to about 2.4.
15. The composition of Claim 12 wherein the polyacrylate is a salt of a homopolymer
of acrylic acid, hydroxyacrylic acid or methacrylic acid, or a copolymer thereof containing
at least about 80% by weight of units derived from said acids.
16. The composition of Claim 12 wherein the polymer has a weight average molecular
weight of from about 3,000 to about 6,000.
17. The composition of Claim 12 wherein the polymer is sodium polyacrylate.
18. The composition of Claim 1 prepared by spray-drying in which the organic detergent
surfactant is in the spray-dried portion.
19. The composition of Claim 1 in the form of a liquid.
20. The composition of Claim 19 which is an aqueous liquid.