TECHNICAL FIELD
[0001] The present invention relates to pouched granular detergent compositions containing
a detergent surfactant, preferably an aluminosilicate ion exchange material, water-soluble
neutral or alkaline hygroscopic builder salt, preferably comprising ether carboxylate
builders as defined herein. The compositions herein, can contain no or only low levels
of phosphate materials and preferably less than about 4% by weight of alkali metal
silicate materials.
BACKGROUND OF THE INVENTION
[0002] Granular detergent compositions have, in the past, often contained high concentrations
of phosphate builder materials, particularly sodium tripolyphosphate. When a crutcher
mix containing sodium tripolyphosphate is spray-dried, it is believed that enough
mixed-phosphate hydrolysis products are formed to inhibit phosphate crystal growth.
The hydrolysis products are concentrated in the liquid phase which finally dries
to an amorphous glassy phosphate material. This glassy material effectively "cements"
the finely crystalline granule walls together, producing granules which exhibit very
desirable physical properties, i.e., crisp, durable and free-flowing granules. Moreover,
the glassy phosphate material readily disintegrates in the laundering solution so
that no insoluble residue is left on the fabrics.
[0003] Alkali metal silicates are usually included in granular detergents at low levels
for corrosion inhibition and processing reasons. When phosphate builders are removed
from detergents, the level of silicate is often increased severalfold since it also
dries to a tough glassy film capable of strengthening granule walls and enhancing
free-flowing characteristics. Silicates having a lower SiO₂ to alkali metal oxide
ratio (e.g. 1.6-2.0) are usually selected because they are more water-soluble than
the higher ratio silicates. However, exposure of the silicate to carbon dioxide during
drying and storage can shift its ratio to a higher value and reduce its solubility,
resulting in detergent granules which do not completely disintegrate in the laundering
solution, and an unacceptably high level of insoluble material being deposited on
fabrics. The insolubles problem can be particularly severe when the detergent composition
also contains water-insoluble aluminosilicate material since higher levels of silicates
(e.g., above about 3%) enhance the deposition of the aluminosilicates onto fabrics.
This solubility problem is compounded further in a pouched detergent form product.
[0004] An annoying problem with air/water-permeable pouched granular detergent is dusting
when the pouch is removed from its package for use in the washing machine.
[0005] The use of hygroscopic builders, particulatly at higher levels, can improve granular
detergent solubility. However, they have been avoided in granular form due to granular
stickiness and caking upon storage. Detergent stickiness and caking are usually associated
with decreased solubility and undesirable flow properties.
SOME OBJECTS OF THE PRESENT INVENTION
[0006] It is therefore an object of the present invention to provide a pouched laundry hygroscopic
granular detergent composition dispenser that is disposable in nature and which will
dispense the laundry detergent in a simple and efficient manner during the wash period
of an automatic clothes washing machine.
[0007] Another object of the present invention is to provide a porous pouched laundry detergent
dispenser with reduced dusting.
BRIEF DESCRIPTION OF THE DRAWINGS
[0008]
Fig. 1 is a perspective view of a water-permeable, water-insoluble laundry active
dispenser with central agitating post loops and containing pouched laundry actives,
which is a preferred pouched dispenser.
Fig. 2 is a top flat view of the pouched laundry active dispenser of Fig. 1.
Fig. 3 is a perspective view of the laundry active dispenser of Fig. 1 positioned
about a central agitating post of an automatic clothes washing machine.
SUMMARY OF THE INVENTION
[0009] The present invention encompasses a porous, pouched hygroscopic granular detergent
composition and a method of dispensing said hygroscopic granular detergent into the
wash water of a washing machine.
DETAILED DESCRIPTION OF THE INVENTION
[0010] The present invention encompasses a porous, pouched hygroscopic granular detergent
composition comprising:
(a) from about 5% to about 45% by weight of an organic surfactant selected from the
group consisting of anionic, nonionic, zwitterionic, ampholytic and cationic surfactants,
and mixtures thereof;
(b) from about 5% to about 75% by weight of water-soluble neutral or alkaline salt
comprising from about 1% to about 55%, by weight of the granular detergent composition,
of a hygroscopic builder salt selected from the group consisting of: organic salts
of citrate, formate, malate, succinate, acetate, tartrate, and ether polycarboxylate
builder having the formula:

wherein each R is selected from the group consisting of H, and OH with no more than
one OH group being attached to any one carbon atom; R¹ is either a group having the
formula

wherein each X is selected from the group consisting of H and cations which make
the ether polycarboxylate builder water soluble and n is from 0 to 4; and said composition
contains less than about 10% by weight of phosphate materials, said composition being
formed by drying a concentrated aqueous slurry comprising the above components; and
(c) from 0% to about 30%, preferably from about 5% to about 25%, by weight of a finely
divided aluminosilicate ion exchange material selected from the group consisting of:
(1) crystalline aluminosilicate material of the formula:
Naz[(A10₂)z(SiO₂)y]·xH₂O
wherein z and y are at least 6, the molar ratio of z to y is from 1.0 to 0.5 and x
is from 10 to 264, said material having a particle size diameter of from about 0.1
micron to about 10 microns, a calcium ion exchange capacity of at least about 200
mg CaCO₃ eq./g and a calcium ion exchange rate of at least about 2 grains Ca⁺⁺/gallon/minute/gram/gallon;
(2) amorphous hydrated aluminosilicate material of the empirical formula:
Mz(zA102ySiO₂)
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 CaCO₃ hardness per gram of anhydrous aluminosilicate
and a Mg⁺⁺ exchange rate of at least about 1 grain/gallon/minute/gram/gallon; and
(3) mixtures thereof; and
wherein said composition is at least initially free flowing, but may become caky
or paste-like upon storage.
[0011] The pouched granular detergent compositions of the present invention contain, as
essential components, detergent surfactant and water-soluble neutral or alkaline hygroscopic
builder salt selected from ether polycarboxylate builders, hygroscopic organic salts
of citrate, formate, malate, succinate, acetate, tartrate, and suitable hygroscopic
polyacrylate salts and mixtures thereof.
[0012] The compositions preferably contain (1 ) from 0% to less than about 5%, more preferably
less than about 4%, most preferably less than about 3%, by weight of alkali metal
silicate materials; and (2) from 0% to less than about 10%, more preferably less than
about 5%, by weight of phosphate materials. Most preferably, the compositions are
substantially free of phosphate materials, at least less than 0.5%. A level of silicate
of up to about 10, preferably up to about 8 can be included if solubility is not an
issue.
[0013] The compositions herein are prepared by drying an aqueous slurry comprising the above
components. The slurry generally contains from about 25% to about 50% water, whereas
the dried granules can contain up to about 15% water, normally initially from about
3% to about 12%. Higher water levels in the slurry give poorer granules. The drying
operation can be accomplished by any convenient means, for example, by using spray-drying
towers, both countercurrent and co-current, fluid beds, flash-drying towers, both
countercurrent and co-current, fluid beds, flash-drying equipment, or industrial microwave
or oven drying equipment. Preferably the drying is in a countercurrent spray drying
tower. The granular detergents herein exhibit at least initial free-flowing characteristics
which are essential for fast line pouching. The presence of hygroscopic and deliquescent
builders will cause caking or stickiness particularly upon storage. The ether polycarboxylate
builders are readily water-soluble and the granules quickly disintegrate in the laundering
solution. Little or no insoluble residue is left on the fabrics. Moreover, the ether
polycarboxylate builder is an effective builder.
[0014] The granular detergents are uniquely suited for pouched detergent articles and a
method of making same. The granular detergents of this invention are free flowing
when made and they are filled into the pouches while free flowing, however, they can
become sticky and nonfree flowing or lumpy under stress storage conditions which makes
them unsuitable for granular detergents in boxes. Surprisingly, notwithstanding increased
caking, there is a benefit in reduced dusting with surprisingly about equal solubility
of the detergent from the pouch. Thus, the combination allows for the use of a detergent
which forms lumps which are otherwise unacceptable for box use. Yet in the present
invention, this sticky, lumpy detergent provides a reduced dusting benefit while
maintaining good solubility from a pouch.
Water-Soluble Neutral and Alkaline Hygroscopic Salts
[0015] The granular detergents of the present invention can contain a total of from about
5% to about 75%, preferably from about 10% to about 60%, and more preferably from
about 20% to about 50%, by weight of a water-soluble neutral or alkaline salt. The
neutral or alkaline salt has a pH in solution of seven or greater, and can be either
organic or inorganic in nature. The salt assists in providing the desired density
and bulk to the detergent granules herein. While some of the salts are inert, many
of them also function as detergency builder materials in the laundering solution.
[0016] Examples of neutral water-soluble salts include the alkali metal, ammonium or substituted
ammonium chorides, fluorides and sulfates. The alkali metal, and especially sodium,
salts of the above are preferred. Sodium sulfate is typically used in detergent granules
and is a particularly preferred salt herein and is used at a level of about 1:1 of
the hygroscopic builder salt.
[0017] Other useful water-soluble salts include the compounds commonly known as detergent
builder materials. Builders are generally selected from the various water-soluble,
alkali metal, ammonium or substituted ammonium phosphates, polyphosphates, phosphonates,
polyphosphonates, carbonates, silicates, borates, and polyhydroxysulfonates. Preferred
are the alkali metal, especially sodium, salts of the above. However, as previously
described, the present compositions should preferably contain less than about 5%,
preferably less than about 4%, more preferably less than about 3% by weight of silicate
materials for optimum solubility and less than about 10%, preferably less than about
5%, by weight of phosphate materials. Most preferably, the compositions are substantially
free of phosphates.
[0018] Specific examples of inorganic phosphate builders are sodium and potassium tripolyphosphate,
pyrophosphate, polymeric metaphosphate having a degree of polymerization of from
about 6 to 21, and orthophosphate. Examples of polyphosphonate builders are the sodium
and potassium salts of ethylene diphosphonic acid, the sodium and potassium salts
of ethane 1-hydroxy-1 ,1-diphosphonic acid and the sodium and potassium salts of
ethane, 1,1,2-triphosphonic acid. Other phosphorus builder compounds are disclosed
in U.S. Pat. Nos. 3,159,581; 3,213,030; 3,422,021; 3,422,137; 3,400,176 and 3,400,148,
incorporated herein by reference.
[0019] Examples of nonphosphorus, inorganic builders are sodium and potassium carbonate,
bicarbonate, sesquicarbonate, tetraborate decahydrate, and silicate having a molar
ratio of SiO₂ to alkali metal oxide of from about 0.5 to about 4.0, preferably from
about 1.0 to about 2.4.
The Hygroscopic Builder Salt
[0020] The water-soluble neutral or alkaline hygroscopic builder salts comprise from about
1% to about 55%, preferably from about 3% to about 30%, most preferably from about
5% to about 25%, by weight of the granular detergent composition.
[0021] The hygroscopic builder salt is selected from the group consisting of: organic salts
of citrate, formate, malate, succinate, acetate, tartrate, and ether polycarboxylate
builder having the formula:

wherein each R is selected from the group consisting of H, and OH with no more than
one OH group being attached to any one carbon atom; R¹ is either a group having the
formula

wherein each X is selected from the group consisting of H and cations which make
the ether polycarboxylate builder water soluble and n is from 0 to 4.
[0022] The preferred hygroscopic builder salts are ether polycarboxylate detergency builders
of the general structural formula:

wherein each R is H or OH, so long as only one OH group is attached to a carbon atom,
and R¹ can be either

wherein each X is H or a salt-forming cation and n is from 0 to 4. These ether polycarboxylate
builder acids or salts thereof are hereinafter designated as "EPB". "EPB" is used
to designate both the acid and salt forms of these materials. When one of the R groups
at either end is OH, n is 1, and the other R's and R¹ are H, the material is identified
as TMS. When all R's are H and n is 2 the material is identified as TDS.
[0023] One preferred composition contains at least 26% by weight of the ether polycarboxylate
builder. Another contains from about 5% to about 35% organic salt of citrate. Yet
another contains from about 3% to about 25% ether polycarboxylate and from about 1%
to about 15% organic salt of citrate, more preferably from about 5% to about 15% ether
polycarboxylate with citrate with a ratio of 2:1 to 1:2.
[0024] It is an additional advantage of the EPBs that they provide synergistic cleaning
performance when combined with the aluminosilicate derergency builder, especially
hydrated Zeolite A with a particle size of less than about 5 microns. The benefit
is greatest for lower levels of EPBs up to a 1:1 ratio of EPB to aluminosilicate.
[0025] The EPB component can be employed in the compositions herein in their free acid form,
i.e., wherein X in the structural formulas is H. Alternatively, and preferably, these
materials can be partially or fully neutralized to a tartrate monosuccinate salt.
Preferred salt-forming cations useful in forming the neutralized materials are those
which yield substantially water-soluble salts of tartrate monosuccinic acid. Examples
of such preferred salt-forming cations include alkali metal (e.g., sodium, potassium,
lithium), C₁-C₄ alkyl substituted ammonium and C₁-C₄ alkanolammonium. The most preferred
salt-forming cations are sodium, potassium, monoethanolammonium and triethanolammonium.
[0026] Specific preferred examples of ether polycarboxylate detergency builders, processes
for making them, etc. are disclosed in U.S. Pat. Application Ser. No. 823,909, filed
Jan. 30, 1986, by Rodney D. Bush, Daniel S. Connor, Stephen W. Heinzman, and Larry
N. Mackey, entitled "Ether Carboxylate Detergency Builders and Process for Their
Preparation," said application being incorporated herein by reference. Other ether
polycarboxylate detergency builders useful herein are disclosed in U.S. Pat. Nos.
3,635,830, Lamberti et al., issued Jan. 18, 1972; 3,784,486, Nelson et al., issued
Jan. 8, 1974; 4,021,376, Lamberti et al., issued May 3, 1977; 3,965,169, Stahlheber,
issued June 22, 1976; 3,970,698, Lannert, issued July 20, 1976; 4,566,984, Bush, issued
Jan. 28, 1986; and 4,066,687, Nelson et al., issued Jan. 3, 1978; all of said patents
being incorporated herein by reference.
Organic Surfactant
[0027] The detergent compositions herein contain from about 5% to about 45% 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 5% to about 45%, and more preferably from about 8% to about
35%, most preferably from about 20 to about 30% by weight of the detergent composition.
Surfactants useful herein are listed in U.S. Pat. No. 3,664,961, Norris, issued May
23, 1972, and in U.S. Pat. No. 3,919,678, Laughlin et al., issued Dec. 30, 1975, both
incorporated herein by reference. Useful cationic surfactants also include those described
in U.S. Pat. No. 4,222,905, Cockrell, issued Sept. 16, 1980, and in U.S. Pat. No.
4,239,659, Murphy, issued Dec. 16, 1980, both incorporated herein by reference. However,
cationic surfactants are generally less compatible with the aluminosilicate materials
herein, and thus are preferably used at low levels, if at all, in the present compositions.
The following are representative examples of surfactants useful in the present compositions.
[0028] 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 alkylolammonium 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.
[0029] Useful anionic surfactants also include the water-soluble salts, preferably the alkali
metal, ammonium and alkylolammonium 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 (C₈-C₁₈ carbon atoms) such as those produced by reducing the glycerides
of tallow or coconut oil; and the sodium and potassium alkyl benzene sulfonates in
which the alkyl group contains from about 9 to about 15 carbon atoms, in straight
or branched chain configuration, e.g., those of the type described in U.S. Pat. Nos.
2,220,099 and 2,477,383. Especially valuable are linear straight chain alkyl benzene
sulfonates in which the average number of carbon atoms in the alkyl group is from
about 11 to 13, abbreviated as C₁₁-C₁₃ LAS.
[0030] 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 wherein the alkyl groups contain from
about 8 to about 12 carbon atoms; and sodium or potassium salts of alkyl ethylene
oxide ether sulfates containing from about 1 to about 10 units of ethylene oxide per
molecule and wherein the alkyl group contains from about 10 to about 20 carbon atoms.
[0031] Other useful anionic surfactants herein 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 about 20 carbon
atoms in the alkane moiety.
[0032] 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.
[0033] 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.
[0034] 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 3 to 8 moles of ethylene oxide per mole of alcohol.
[0035] Semi-polar nonionic surfactants include water-soluble amine oxides containing one
alkyl moiety of from about 10 to 18 carbon atoms and 2 moieties selected from the
group consisting of alkyl groups and hydroxyalkyl groups containing from 1 to about
3 carbon atoms; water-soluble phosphine oxides containing one alkyl moiety of about
10 to 18 carbon atoms and 2 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.
[0036] Ampholytic surfactants include derivatives of aliphatic or aliphatic derivatives
of heterocyclic secondary and tertiary amines in which the aliphatic moiety can be
either straight or branched chain 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.
[0037] 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.
[0038] Particularly preferred surfactants herein include linear alkylbenzene sulfonates
containing from about 11 to 14 carbon atoms in the alkyl group; tallowalkyl sulfates;
coconutalkyl glyceryl ether sulfonates; alkyl ether sulfates wherein the alkyl moiety
contains from about 14 to 18 carbon atoms and wherein the average degree of ethoxylation
is from about 1 to 4; olefin or paraffin sulfonates containing from about 14 to 16
carbon atoms; alkyldimethylamine oxides wherein the alkyl group contains from about
11 to 16 carbon atoms; alkyldimethylammonio propane sulfonates and alkyldimethylammonio
hydroxy propane sulfonates wherein the alkyl group contains from about 14 to 18 carbon
atoms; soaps of higher fatty acids containing from about 12 to 18 carbon atoms; condensation
products of C₉-C₁₅ alcohols with from about 3 to 8 moles of ethylene oxide, and mixtures
thereof.
[0039] Specific preferred surfactants for use herein include: sodium linear C₁₁-C₁₃ alkylbenzene
sulfonate; triethanolammonium C₁₁-C₁₃ alkylbenzene sulfonate; sodium tallow alkyl
sulfate; sodium coconut alkyl glyceryl ether sulfonate; the sodium salt of a sulfated
condensation product of a tallow alcohol with about 4 moles of ethylene oxide; the
condensation product of a coconut fatty alcohol with about 6 moles of ethylene oxide;
the condensation product of tallow fatty alcohol with about 11 moles of ethylene
oxide; the condensation of a fatty alcohol containing from about 14 to about 15 carbon
atoms with about 7 moles of ethylene oxide; the condensation product of a C₁₂-C₁₃
fatty alcohol with about 3 moles of ethylene oxide; 3-(N,N-dimethyl-N-coconutalkylammonio)-2-hydroxypropane-1-sulfonate;
3-(N,N-dimethyl-N-coconutalkylammonio)-propane-1-sulfonate; 6-(N-dodecylbenzyl-N,N-dimethylammonio)
hexanoate; dodecyldimethylamine oxide; coconutalkyldimethylamine oxide; and the water-soluble
sodium and potassium salts of coconut and tallow fatty acids.
Aluminosilicate Ion Exchange Material
[0040] The detergent compositions herein can also contain from 0% to about 30%, preferably
from about 5% to about 25%, and more preferably from about 5% to about 20%, by weight
of crystalline aluminosilicate ion exchange material of the formula
Na
z[(A10₂)
z(SiO₂)
y]
·xH₂O
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
M
z(zA10
2ySiO₂)
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 CaCO₃ hardness per gram of anhydrous
aluminosilicate. Hydrated sodium Zeolite A with a particle size of from about 1 to
10 microns is preferred.
[0041] 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 by weight 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 CaCO₃ 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/minute/gram/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.
[0042] The amorphous aluminosilicate ion exchange materials usually have a Mg⁺⁺ exchange
of at least about 50 mg eq. CaCO₃/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).
[0043] 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. Pat. No. 3,985,669, Krummel et al., issued Oct. 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 has the formula
Na₁₂[(A10₂)₁₂(SiO₂)₁₂]
·xH₂O
wherein x is from about 20 to about 30, especially about 27 and has a particle size
generally less than about 5 microns.
Disposable Dispenser Pouches
[0044] One type of dispenser for introducing laundry actives into the wash water in automatic
washers is a free-bodied dispenser disclosed in U.S. Pat. No. 4,348,293, Clarke et
al., issued Sept. 7, 1982, and commonly assigned U.S. Pat. Application Ser. No. 017,103,
Hortel et al., filed Feb. 19, 1987, now allowed, both incorporated herein by reference.
A preferred disposable dispenser is designed to be removably attached to the central
agitating post of a washing machine for dispensing a laundry active, e.g., a detergent
or bleach, into the wash water of the machine.
[0045] According to the invention herein, a preferred disposable dispenser is provided for
the dispensing of a laundry active during the wash period of an automatic clothes
washing machine having an upright central agitating post. The dispenser comprises
a sealed water-permeable, water-insoluble pouch or container, adaptable to being
fastened onto the central agitating post and having disposed therein a laundry additive.
The laundry active dissolves out of said water-permeable container by force of the
agitating post and wash water. By employing such a dispenser, the consumer can be
given the improved solubility performance as from free-bodied contained laundry active
dispensers, and at the same time obtain the convenience of nonhandling of the laundry
active itself, and the ease of disposing the container once it has been used. Moreover,
such a dispenser is easy to handle, economical to manufacture at a low cost to the
consumer, and safe to use.
[0046] For the purposes of expediency, the invention can be best explained and described
by referring to a preferred embodiment thereof which is the subject matter of the
accompanying drawings. It is to be understood that the scope of the invention is not
to be limited thereto.
[0047] Referring now to Figs. 1 and 2, a preferred embodiment of a laundry active dispenser
10 is shown having two equal laminated rectangular sheets, 12 and 14. The sheets are
made of a flexible laminar water-permeable, water-insoluble material permanently sealed
together at their peripheral edges 11 in this particular instance, by means of a continuous
heat seal 16. It is not intended , however, to limit the present embodiment to such
flexible laminar materials, or to the provision of a heat sealing means. Referring
to Fig. 1, the two laminar sheets are also joined together by means of heat seals
16 and 18 to divide the dispenser 10 into four rectangular container pouches 26 and
28′.
[0048] Referring to Figs. 1 and 2, the preferred dispenser is made by first embossing one
of the substrate sheets, e.g., 14, to form deeper pochets for the pouches to contain
the laundry active ingredients. Next, the ingredients are placed in the indentations
created by the embossing. A sheet of polyethylene film (not shown) can be precut to
match the seal areas 16 and 18 which are around and between the pouch pockets 26 and
28. This sheet is placed in position to line up with the embossed sheet. The second
sheet 12 is then put in place and heat is applied to the embossed sheet. The heat
melts the polyethylene film and seals the laundry actives inside the pouched pockets.
The seals 16 and 18, in conjunction with the laminar sheets 12 and 14, form the sealed
container pouches 26 and 28 having the laundry additives 29 and 31 disposed therein.
See U.S. Pat. No. 4,638,907, Bedenk et al., issued Jan. 27, 1987, incorporated herein
by reference, for more details on how embossed, pouched laminated dispensers are made.
[0049] The top and bottom peripheral edges 20 and 21 have slits 22 and 23 so as when opened,
circular loops 22′ and 23′ are formed which are large enough to be loosely fitted
(fastened) about the central agitating post 24 of an automatic clothes washing machine
(see Fig. 3) An advantage of having two circular loops 22′ and 23′ is that the dispenser
10 is held more closely to the agitator. In a modified dispenser 10, the container
pouches 26 and 28 can be designed so that the dispenser is perforated (not shown)
so it could be torn in half or used in larger or smaller loads. Each half would have
a circular loop for fastening to the agitator post.
[0050] In order to provide dissolution and egress of the laundry actives 29 and 31 from
their container pouches 26 and 28 into the automatic clothes washing machine (not
shown) during the operation of the wash period, at least one of the two sheets 12
and 14 that forms the container pouches 26 and 27 of the dispenser 10 is water-permeable.
It will be noted that the slits 22 and 23 do not extend across the entire length of
the sheets' peripheral edges 11. The object to be kept in mind, in accordance with
the invention, is to provide a means to fasten the dispenser to the central post
24 to allow the laundry active to dispense from its container pouches in response
to the movement of the central agitating post. Preferably, the seals do not rupture.
Accordingly, the nature of materials used for making the dispenser 10 should be so
selected.
[0051] Accordingly, the operation of the preferred laundry active dispenser is simply begun
by looping the dispenser onto the central agitating post 24, preferably before the
operation of the machine has been initiated, in the manner shown in Fig. 3. Once the
machine is started, it will be seen that the dispenser is activated by the wash period
of the automatic washer. After the automatic washer has gone through its complete
operation, the used dispenser can be lifted off the central agitating post and discarded
or placed in the dryer with the washed fabrics.
[0052] In view of what has been described hereinbefore as a preferred embodiment, it will
be appreciated that other forms and embodiments are also within the scope of the present
invention. Several of the critical features that must be inherent in the type of dispenser
previously described and employed to dispense the laundry additive are that the laundry
active(s) can be coated on or completely enclosed in the dispenser for release in
the wash cycle. There must be a potential for water-permeability in the unit to allow
dissolution and egress of the laundry active(s) into the wash aided by the agitation
force of the central agitating post acting upon the unit.
[0053] Accordingly, any number of materials other than a flexible laminar nonwoven substance
can be used for the container to enclose the laundry active, for example, porous metal
foils, porous plastic bags, and the like. The material used, however, must be compatible
with the nature of the laundry active which it is to contain, so that the chemical
or physical identity of the container itself or the laundry active is not altered.
[0054] With the above in mind, other materials can be used, such as porous foil sheeting,
paper sheeting, porous plastic boxes, nonwoven or woven cloth sheeting.
[0055] With regard to the attachment or fastening of the dispenser to the central agitating
post of the automatic washer, any number of methods or means that are compatible with
the dispenser design and provides for a means to fasten the dispenser to allow exit
of the active from the water-permeable, water-insoluble container into the wash water
through agitation force can be used. See U.S. Pat. No. 4,026,131,
supra, for suitable fastening means designs.
[0056] In addition to the above embodiments, the present invention can be combined with
dispenser devices which are activated in the spin period or the rinse period of the
washing machine operation or the drying operation. In this respect, reference is made
to U.S. Pat. No. 4,026,131,
supra, and commonly assigned U.S. Ser. No. 017,103, Hortel et al.,
supra, both incorporated herein by reference in their entirety.
EXAMPLE I
[0057] One example of the present invention is a laundry active dispenser 10 shown in Figs.
1, 2 and 3. This laundry active dispenser has been constructed so it can be packed
flat and when used easily slipped over the top of the washing machine central post
agitator, where it remains throughout the wash cycle. Dispenser 10 is 4-1/2 inches
(11.4 cm) tall. The circumferences of loops 22′ and 23′ are about 21 inches (5.3 cm),
which is large enough to easily fit over virtually every washing machine central post
agitator. It is also large enough to slip half way or more down on the central post
agitator so that when the consumer wants to use the machine to wash a small load,
which requires low water fills, the dispenser and its contained laundry additives
will be submerged and can dissolve.
[0058] This example is constructed of materials that are strong enough to survive the reciprocal
agitation and centrifugal spin forces of the washer cycle. It is then put in the dryer
along with the wet laundry to dispense water-insoluble through the wash and rinse
fabric softening and antistatic agents that have been designed to survive the wash
and be activated by the heat of the dryer. The substrate used in this example is a
spun-bonded polyester nonwoven supplied by DuPont under the trade name Reemay® 2420.
For a list of suitable detergent and bleach additives, softeners and substrates, see
allowed U.S. Ser. No. 017,103,
supra, incorporated herein by reference.
[0059] This dispenser 10 also has multiple pouches (pockets). Each one can be used to hold
one or more laundry actives, for example, laundry detergent, bleach, enzymes, optical
brighteners, builders and other chemicals used to clean and condition laundry in the
washer.
Optionals
[0060] Other ingredients commonly used in detergent compositions can be included in the
compositions of the present invention. These include flow aids, color speckles, bleaching
agents and bleach activators, suds boosters or suds suppressors, antitarnish and anticorrosion
agents, soil suspending agents, soil release agents, dyes, fillers, optical brighteners,
germicides, pH adjusting agents, nonbuilder alkalinity sources, hydrotropes, enzymes,
enzyme-stabilizing agents, chelating agents and perfumes.
[0061] The compositions of this invention need not be packaged in containers with good or
excellent moisture barrier properties by virtue of unit doses contained in pouches.
[0062] Materials like sodium perborate tetrahydrate and monohydrate can be admixed with
the granular detergent compositions of this invention. Other materials include enzymes,
solid hydrogen peroxide sources, hydrogen peroxide activators, and silicone suds suppressors.
[0063] The following nonlimiting examples illustrate the detergent compositions of the present
invention.
[0064] All percentages, parts, and ratios used herein are by weight unless otherwise specified.
TABLE 1
Formula Examples (by parts) |
|
No. 1 |
No. 2 |
No. 3 |
No. 4 |
C₁₃ Linear alkyl benzene sulfonate |
13.7 |
11.2 |
10.1 |
15.0 |
C₁₄-C₁₅ Alkyl sulfate |
13.7 |
11.2 |
10.1 |
15.0 |
Sodium sulfate |
17.8 |
14.5 |
13.2 |
19.5 |
Tergitol 80-L50N* |
2.1 |
1.8 |
1.6 |
2.3 |
Sodium polyacrylate (Avg. M.W. approx. 4500) |
1.6 |
1.3 |
1.1 |
1.7 |
Polyethylene glycol (Avg. M.W. approx. 8000) |
1.6 |
1.3 |
1.1 |
1.7 |
|
Ether polycarboxylate builder TMS/TDS, sodium salt 86:14 weight ratio TMS:TDS |
10.6 |
31.8 |
30.1 |
0.0 |
Zeolite A** |
15.8 |
13.0 |
11.7 |
17.3 |
Sodium citrate |
9.5 |
0.0 |
6.9 |
20.2 |
Impurities, etc. |
6.4 |
7.0 |
7.0 |
0.0 |
Unreacted |
0.6 |
0.6 |
0.5 |
0.8 |
Water |
6.4 |
6.4 |
6.4 |
6.4 |
*Tergitol 80-L50N is an ethoxylated/propoxylated 5.3 EO and 0.9 PO, approximately
with alkyl chain lengths of C₈ (20%) to C₁₀ (80%). |
**Zeolite A is defined hereinabove. |
[0065] The above formulas are prepared by making a crutcher mix of the base granule ingredients
with a water level of about 40% and spray drying. It highly desirable to insure good
inital flowability by adding a flow aid, 0.1-1 parts, to the spray dried granules.
Some preferred flow aids are anhydrous and particulate colloidal silica, e.g., Cab-O-Sil
(Cabot Corp.) and Sipernatt, available commercially. The spray dried base granules
are packaged in water-permeable, water-insoluble unit dose pouches. It is also desirable
to admix any optionals to the base granules prior to pouching.
[0066] The pouched base detergent granule compositions of the present invention are initially
free flowing, but become lumpy or sticky upon storage under stress conditions, e.g.,
80°F (27°C)/60-80% relative humidity. One test is to store the pouches in a closed
cardboard box for a period of several weeks. The pouches are then examined for caking
and stickiness after the first, second and fourth weeks. Tile pouches are also tested
for dust grades. The pouched compositions of the present invention provide very good
detergent solubility with improved dusting after stress storage, notwithstanding the
development of lumpiness.
1. A porous, pouched detergent composition comprising:
(a) from about 5% to about 45% by weight of an organic surfactant selected from the
group consisting of anionic, nonionic, zwitterionic, ampholytic and cationic surfactants,
and mixtures thereof;
(b) from about 5% to about 75% by weight of water-soluble neutral or alkaline salt
comprising from about 1% to about 55%, by weight of the granular detergent composition,
of a hygroscopic builder salt selected from the group consisting of: organic salts
of citrate, formate, malate, succinate, acetate, tartrate, and ether polycarboxylate
builder having the formula:

wherein each R is selected from the group consisting of H, and OH with no more than
one OH group being attached to any one carbon atom; R¹ is either a group having the
formula

wherein each X is selected from the group consisting of H and cations which make
the ether polycarboxylate builder water soluble and n is from 0 to 4; and said composition
contains less than about 10% by weight of phosphate materials, said composition being
formed by drying a concentrated aqueous slurry comprising the above components; and
(c) from 0% to about 30% by weight of a finely divided aluminosilicate ion exchange
material selected from the group consisting of:
(1) crystalline aluminosilicate material of the formula:
Na
z[(A10₂)
z(SiO₂)
y]
·xH₂O
wherein z and y are at least 6, the molar ratio of z to y is from 1.0 to 0.5 and x
is from 10 to 264, said material having a particle size diameter of from about 0.1
micron to about 10 microns, a calcium ion exchange capacity of at least about 200
mg CaCO₃ eq./g and a calcium ion exchange rate of at least about 2 grains Ca⁺⁺ /gallon/minute/gram/gallon;
(2) amorphous hydrated aluminosilicate material of the empirical formula:
M
z(zA10
2ySiO₂)
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 CaCO₃ hardness per gram of anhydrous
aluminosilicate and a Mg⁺⁺ exchange rate of at least about 1 grain/gallon/minute/gram/gallon;
and
(3) mixtures thereof; and
wherein said composition is at least initially a free flowing granule and is contained
in said porous pouch.
2. A porous, pouched detergent composition according to Claim 1 comprising from about
20% to about 35% by weight of said organic surfactant and said pouch comprises a water-permeable,
water-insoluble substrate.
3. A porous, pouched detergent composition according to Claim 1 wherein said organic
surfactant is selected from the group consisting of linear alkylbenzene sulfonates
containing from about 11 to 14 carbon atoms in the alkyl group, tallowalkyl sulfates;
coconutalkyl glyceryl ether sulfonates; alkyl ether sulfates wherein the alkyl moiety
contains from about 14 to 18 carbon atoms and wherein the average degree of ethoxylation
is from about 1 to 4; olefin or paraffin sulfonates containing from about 14 to 16
carbon atoms; alkyldimethyl amine oxides wherein the alkyl group contains from about
11 to 16 carbon atoms; alkyldimethylammonio propane sulfonates and alkyldimethylammonio
hydroxy propane sulfonates wherein the alkyl group contains from about 14 to 18 carbon
atoms; soaps of higher fatty acids containing from about 12 to 18 carbon atoms; condensation
products of C₉-C₁₅ alcohols with from about 4 to 8 moles of ethylene oxide, and mixtures
thereof.
4. A porous, pouched detergent composition according to Claim 1 comprising from about
5 to about 25% by weight of said crystalline aluminosilicate material and wherein
said crystalline aluminosilicate material is of the formula
Na₁₂[(A10₂)₁₂(SiO₂)₁₂]·xH₂O
wherein x is from about 20 to about 30.
5. A porous, pouched detergent composition according to Claim 1 comprising from about
3% to about 25% by weight of said ether polycarboxylate builder and from about 1%
to about 25% of an organic salt of citrate.
6. A porous, pouched detergent composition according to Claim 1 comprising from about
5% to about 15% by weight of said ether polycarboxylate builder wherein said polycarboxylate
and said citrate have a ratio of from about 2:1 to about 1:2.
7. A porous, pouched detergent composition according to Claim 1 comprising from about
10% to about 60% by weight of said water-soluble neutral or alkaline salt and wherein
the water-soluble neutral or alkaline salt comprises sodium sulfate and from about
3% to about 20% by weight of said ether polycarboxylate builder.
8. A porous, pouched detergent composition according to Claim 1 containing from 0%
up to less than about 5% by weight of phosphate materials and from 0% up to less than
about 4% by weight of alkali metal silicate materials.
9. A porous, pouched detergent composition according to Claim 1 comprising at least
26% by weight of said ether polycarboxylate builder.
10. A porous, pouched detergent composition according to Claim 1 containing from about
5% to about 35% by weight said organic salt of citrate.