[0001] This invention relates to compositions and methods for preventing fabric encrustation
by decreasing or suppressing the formation of encrustation residue when using detergent
applications and formulations during fabric washing operations with "hard water."
In particular, this invention relates to the use of certain organic dicarboxylic acids
to prevent growth or deposition of insoluble compounds on fabric surfaces during washing
operations. The invention is primarily concerned with inhibition of the formation
and deposition of insoluble compounds on fabric.
[0002] The growth of insoluble compounds on fabric surface (fabric encrustation) from repeated
washing with non-phosphate detergents in "hard water" is a negative effect in which
the appearance and feel of the fabric are affected. The fabric acquires a rough feel
and colored garments have a faded appearance.
[0003] The insoluble compounds primarily are calcium and magnesium carbonate precipitates
caused by builders, such as sodium carbonate, typically used in non-phosphate detergents.
Therefore, the prevention of encrustation or the deposition of insoluble compounds
formed during the washing process with "hard water" is strongly desired. Phosphonates
and polyacrylates have been shown to be effective in detergent applications for the
prevention of encrustation. Phosphonates can function as crystal growth inhibitors
which prevents the growth of insoluble calcium and magnesium compounds at substoichiometric
concentrations. Polyacrylates can function as sequestering and dispersing agents,
as well as crystal growth inhibitors. Some drawbacks associated with phosphonates
and polyacrylates are that phosphonates can contribute to euthrophication and polyacrylates
are not biodegradable.
[0004] Heavy-duty laundry detergents typically contain two major ingredients, surfactant
and builder, and a number of other ingredients essential to an acceptable product.
Although of lesser importance to detergency, these additional ingredients impart certain
desirable functions to the total formulated detergent. These miscellaneous ingredients
include anti-corrosion agents, anti-soil redeposition agents, fluorescent whitening
agents, bleaches, enzymes, perfume and the like. The two major components most essential
to detergency are surfactant and builder.
[0005] The surfactant provides detersive action to the detergent. This is based on their
fundamental characteristic to absorb or concentrate at the soil/fiber/water interfaces.
The detergent builder functions primarily to prevent divalent calcium and magnesium
water-hardness ions from interfering with the surfactant action. The builder also
may provide alkalinity thus improve fatty acid saponification and buffering capacity,
prevent flocculation, maintain ionic strength, extract metals from soils and remove
alkaline-earth metal ions from the washing solutions. Phosphates are extremely effective
builders; however, they are in disfavor due to their eutrophication effect on lakes
and streams. Many states in the United States have enacted legislation limiting phosphate
content. Such legislation to reduce phosphate content has led to a variety of non-phosphate
builders, either proposed and/or employed. Examples include silicates, zeolites, carbonates
and polycarboxylates, citrates, EDTA and sodium nitrilotriacetate (NTA). Such alternatives
are themselves subject to various limitations. Silicates are not preferred because
they are not entirely water-soluble and they can therefore deposit onto fabrics, and
also can form precipitates with the hardness ions. Zeolites are generally effective
co-builders, but not necessarily as the sole builder. Polycarboxylate builders are
costly.
[0006] High levels of alkali-metal carbonates have been found to be an effective non-phosphate
builder, particularly in applications where a high pH is required, e.g., for oily
soil removal. A drawback associated with such high carbonate levels is that calcium
and magnesium ions present in the washing water readily form precipitates with the
carbonates,and such precipitates deposit and/or form on the fabrics. These precipitates
leave the fabrics with a rough feel and faded appearance. Various approaches have
been employed in the art to combat the formation of calcium or magnesium precipitates,
including the addition of seed crystals, crystal growth inhibitors and non-precipitating
sequestrants. Non-precipitating sequestering and complexing agents tend to be expensive
due to the stoichiometric levels needed, adding significantly to the overall formula
cost.
[0007] U.S. Pat. 3,896,056, Benjamin et al., relates to a built detergent compositions which
contain as essential ingredients, an organic surface-active agent; a precipitating
builder; and a precipitation modifier. This patent describes a functional test to
assess the ability of compounds to prevent the formation of precipitation as an indication
of its effectiveness as a crystal growth inhibitor. A detergent matrix consisting
of an inorganic precipitating builder is used. A number of polycarboxylic acid compounds
are disclosed as precipitation modifiers.
[0008] U.S. Pat. 4,097,016, Brahm, J., et al., relates to a solid composition for washing,
cleaning and bleaching, including at least one basic compound, as a solid polylactone
is a sequestering agent and can include activators for per-salts, such as anhydrides
of organic acids, succinic acid, phthalic acid, and the like.
[0009] U.S. Pat. 4,814,102, Baur, R. et al., describes copolymers consisting of acrylic,
maleic, furmaric, itaconic or hydroxy alkyl esters of these acids as builders, encrustation
inhibitors, or dispersents in detergents.
[0010] Non-phosphate detergent formulations are disclosed in numerous patents. Larrabee
et al., EP 130,640, discloses a laundry detergent comprising a surfactant, 5 to 80%
of a non-phosphorus detergent builder which may be a carbonate, and about 0.3 to 5%
of a polyacrylate polymer. EP 137,669, Kermode et al., describes a detergent composition
including 5 to 60% of a surfactant, 7 to 80% of a polycarboxylate/zeolite builder,
and a bleach system.
[0011] DeRider et al., EP 82 564, discloses machine dishwashing and rinsing compositions
having nonionic detergent surfactants, a water-soluble calcium sequestering agent,
specific polymeric material and an alkaline detergent material to produce a composition
which has improved non-filming, non-spotting or non-streaking properties. The calcium
sequestering agents are taught to be an organic builder salt, such as water-soluble
citrates, water-soluble salt of nitrilotriacetic acid (NTA), water-soluble salt of
carboxymethoxy succinic acid, or other builders such as zeolites, or organic chelating
agents.
[0012] EP 82 564 shows an example of the calcium sequestering agent; dipicolinic acid is
disclosed as not causing filming on dishes. Similarly, in U.S. 3,850,852, Neillie
et al., sodium carbonate is combined with polyacrylate, phosphonate, and a calcium
sequestering agent.
[0013] EP 233 730, Sanderson et al. discloses the use of 2,6-pyridine dicarboxylic acid
as a chelating stabilizer for potassium sulfoperoxybenzoate in detergent compositions.
This is necessary in the situation where inorganic or organic peroxy acids are unstable
in the presence of nonionic surfactants. It was not feasible to contemplate storing
liquid compositions containing both components without the use of a chelating peroxidic
stabilizer such as dipicolinic acid.
[0014] EP 266 904, Frankena, H., relates to machine dishwashing compositions comprising
low or zero phosphates using dipicolinic acid derivatives as the builder. Also provided
for are enzymes to increase performance.
[0015] The prior art describes polymers of aliphatic polycarboxylic acids as builders in
detergent formulations. However, it has not been recognized that substoichiometric
concentrations of the monomeric forms of some of these compounds alter the kinetics
or crystalline morphology of calcium carbonate, and hence can be used to prevent industrial
scaling, and reduced fabric encrustation in non-phosphorus detergent formulations.
In view of the art cited, there remains a need for compositions and methods for effectively
preventing fabric encrustation in detergent applications and formulations. Compounds
of the present invention are primarily effective at preventing encrustation of fabrics
in high-carbonate, non-phosphorus detergent. Therefore, the present invention provides
an alternative to phosphonate and polyacrylates for prevention of encrustation.
[0016] The present application relates to the compositions and method for using certain
organic dicarboxylic acids and water-soluble derivatives thereof as effective fabric
encrustation preventatives in detergent applications and formulations. The prior art
relates only to the use of certain organic dicarboxylic acids to reduce hardness of
water, or as a stabilizer against degradation of peroxy bleaching compounds. Clearly,
the addition of certain organic dicarboxylic acid and their water-soluble salts and
anhydrides into detergent compositions in order to decrease and/or suppress the formation
of encrustation residue in fabrics from hard water minerals due to the presence of
the sodium carbonate builder in the detergent formulation is not contemplated by the
prior art.
[0017] A leading inorganic replacement for phosphate builders is sodium carbonate. However,
high carbonate content non-phosphate builders produce the problem of "hard water"
precipitates from the calcium and magnesium ions present in the "hard water." The
growth or deposition of the precipitates on the fabrics during washing application
make carbonate-based detergents, otherwise, not preferred.
[0018] It is therefore an object of the present invention to provide a cleaning composition
which does not utilize phosphate builders.
[0019] It is another object of the present invention to provide a high carbonate cleaning
composition which results in reduced levels of calcium and magnesium salt deposition
on fabrics.
[0020] It is another object of the present invention to provide a biodegradable, entirely
non-phosphorus-containing compound which prevents carbonate salt precipitation and/or
controls encrustation.
[0021] It is another object of the present invention to provide a cleaning composition which
provides stain and soil removal performance.
[0022] It is another object of the present invention to provide a cleaning composition and
method for the reduction of fabric encrustation which does not contribute to euthrophication
and is biodegradable. of fabric encrustation when using high carbonate or non-phosphate
detergent formulations.
[0023] It has now been found that by using the compositions and method in accordance with
the present invention, fabric encrustation can be reduced or eliminated when using
high carbonate, non-phosphate detergents with water containing calcium and/or magnesium
ions. The compositions and method are characterized by utilizing certain water-soluble
organic dicarboxylic acids, anhydrides, salts and derivatives thereof. More preferably,
this invention relates to the use of certain organic dicarboxylic acids, water-soluble
salts and anhydrides thereof, especially ketomalonic acid, hydroxymalonic acid and
2,6-pyridine dicarboxylic acid in the detergent compositions and methods utilizing
said compositions.
[0024] More particularly, this invention relates to the use of detergent compositions which
contain ketomalonic acid and 2,6-pyridine dicarboxylic acid or a water-soluble salt
thereof with monovalent cations in a concentration of from about 1 to about 20 percent
by weight, preferably from about 2 to about 12 percent by weight.
[0025] Alkali metal salts, particularly sodium salts, potassium salts or ammonium salts,
can be used as water-soluble salts of the organic dicarboxylic acids of the instant
invention having monovalent cations. Ammonium ions also can be regarded as monovalent
cations for the purpose of the present invention. It is noted that for the purpose
of the present invention the acid or anhydride forms of the organic dicarboxylic acids
are equivalent to the salt forms except where the acid has limited solubility. It
is understood that the anhydride can hydrolyze to form the diacid
in situ. It is also noted that except where explicitly stated or implied from the context,
the acid and salt forms are used interchangeably. It is further noted that if the
organic dicarboxylic acid derivative is added as a water-soluble salt, the required
weight percentage range will be higher than that of the acid, due to the presence
of the counter ion.
[0026] Therefore, in one embodiment, the present invention can be described as a cleaning
detergent composition comprising (a) an alkali-metal carbonate builder; and (b) a
fabricencrustation prohibiting amount of an organic dicarboxylic acid,anhydride or
salt thereof.
[0027] Alkali-metal carbonate. The alkali metal carbonate is the primary and may be the only builder material of
the composition of the present invention. As used herein, the primary builder is defined
as that builder which, in total amount, has the higher capacity for hardness ions
(e.g., calcium (+2) and magnesium (+2)). The term "co-builder" will refer to any remaining
builder which has the lesser capacity (typically less than 30%) for such ions. Alkali
metal carbonates, sesquicarbonates and bicarbonates are suitable primary builders;
however, the preferred builders are sodium and/or potassium carbonates. A building
effective amount of carbonate is present in the compositions herein, which is defined
as that amount of alkali metal carbonates, as the primary builder, which would precipitate
in the presence of hardness ions, in solution, during a wash period at 50°C and 250
ppm hardness. Such precipitation is determined by an increase in solution turbidity
as indicated by an abrupt change in percent transmittance versus time (defined additionally
hereinafter). Generally, in terms of weight percent, and assuming 68 liters of wash
water and about 100 g of composition, at least about 30 percent, preferably 40 percent,
most preferably 50 percent carbonate is employed. As used herein, unless otherwise
stated, all percentages are weight percentages of actives of the total composition.
Higher levels of carbonate will function, however, at levels greater than about 80
percent there is insufficient room for the other ingredients which contribute to the
overall effectiveness of the composition. The carbonate acts as the builder to remove
divalent metal ions such as calcium, and additionally provides alkalinity and aids
in soil removal. At the high levels disclosed herein, the alkali metal carbonate provides
good cleaning performance and in situations requiring a high pH, such as oily soils,
the carbonate builder may be superior to other builders.
Organic Dicarboxylic Acid Encrustation Preventative System
[0028] The preventative system comprises substoichiometric levels of an organic dicarboxylic
acid, water-soluble salt or anhydrides thereof, which act to inhibit fabric encrustation.
For purposes herein, substoichiometric levels of the certain organic dicarboxylic
acid are defined to mean levels which are not able to prevent the precipitation of
calcium and magnesium carbonate by sequestering water hardness ions. For example,
such levels generally comprise less than about 30 percent, more preferably less than
about 20 percent, of the total building capacity.
[0029] By the term "organic dicarboxylic acid" it is meant an organic compound having at
least 2 carboxyl groups. The certain and particular organic dicarboxylic acid compounds
of this invention relate to the following general formulae

wherein
R is selected from the group consisting of 2,3-pyridenyl, 2,4-pyridenyl, 2,6-pyridenyl,
1,2-phenylene, 1,3-phenylene and

wherein R′ and R˝ are independently H, -OH or lower alkyl having 1-4 carbon atoms,
inclusive or R′ and R˝ taken together are oxygen;
n is an integer from from 0 to 3, inclusive;
m is an integer from 0 to 2 when R′ is -OH; and
M₁ and M₂ are independently selected from the group consisting of sodium, potassium,
lithium and ammonium.
[0031] In a second embodiment, the cleaning composition comprises a detergent composition
including:
(a) an alkali-metal carbonate builder;
(b) in encrustation prevention system comprising substoichiometric levels of organic
dicarboxylic acid, water-soluble salts and anhydrides thereof; and
(c) a surfactant.
[0032] Components (a) and (b) are as described previously with respect to the first embodiment.
Component (c) is further described below.
Surfactant
[0033] A myriad of surfactants are known to be suitable for laundry applications, including
anionic, cationic, nonionic and amphoteric surfactants. Preferred surfactants are
anionic, nonionic and mixtures thereof, and if added are present in a cleaning-effective
amount. Preferred anionics are selected from surfactants such as alkali metal alkyl
sulfates, primary and secondary alkane sulfonates, linear alkyl benzene sulfonates,
alkyl ether sulfates, and mixtures thereof. These anionic surfactants will preferably
have alkyl chain groups averaging about 8 to 18 carbon atoms. The preferred anionic
surfactant is a LAS having an alkyl group averaging 8 to 18 carbons. Commercial sources
of such surfactants are the Stephan Chemical Company (Northfield, IL) and the Vista
Chemical Company (Houston, TX). An additionally preferred anionic surfactant, principally
for its cleaning effectiveness, is a secondary alkane sulfonate. An example of a particularly
preferred secondary alkane sulfonate is HOSTAPUR SAS, a trademarked product manufactured
by Farbwerke Hoechst A.G. (Frankfurt, West Germany).
[0034] It is most preferred to include with the anionic surfactant at least one nonionic,
especially C₁₋₄ alkoxylated aliphatic alcohols and C₁₋₄ alkoxylated alkyl phenols.
Particularly preferred are ethoxylated/propoxylated C₈₋₁₄ alcohols. There should be
at least about three alkoxy groups per alcohol, preferably at least about nine. Examples
of preferred ethoxylated/propoxylated aliphatic alcohols are BASF Corporation's (Parsippany,
NJ) trademarked INDUSTROL, and PLURAFAC. Certain C₁₋₄ alkylene oxide copolymers such
as ethylene oxide/propylene oxide copolymers are also preferred as surfactants. These
are exemplified by BASF's trademarked PLURONIC series. Other suitable nonionic surfactants
are polyethoxylated alcohols manufactured and marketed by the Shell Chemical Company
(Houston, TX) under the trademark NEODOL. Examples of preferred NEODOLS are NEODOL
25-7 which is a mixture of 12 to 15 carbon chain length alcohols with about 7 ethylene
oxide groups per molecule, NEODOL 23-65, a C₁₂₋₂₃ mixture with about 6.5 moles of
ethylene oxide, and NEODOL 25-9, a C₁₂₋₁₅ mixture with about 9 moles of ethylene oxide.
Also useful are a trimethyl nonyl polyethylene glycol ether, manufactured and marketed
by Union Carbide Corporation under the trademark TERGITOL TMN-6, and an octyl phenoxy
polyethoxy ethanol sold by Rohm and Haas (Philadelphia, PA) under the trademark TRITON
X-114. Total surfactant content is preferably from 0.1% to about 20%, more preferably
from about 2% to 15%.
[0035] In a third embodiment, the present invention comprises a dry, granular laundry detergent
composition comprising:
(a) an alkali-metal carbonate builder;
(b) certain organic dicarboxylic acid or a water-soluble salt thereof as encrustation
inhibitor system;
(c) a surfactant;
(d) a bleach;
(e) an alkali-metal silicate;
(f) a filler; and
(g) laundry adjuncts.
Elements (a), (b) and (c) are as described in the first and second embodiments. Elements
(d) through (g) are further described hereinbelow.
Bleach
[0036] Preferred peroxygen bleaches are available in solid form and include sodium percarbonate,
sodium perborate, sodium phosphate peroxyhydrate, potassium permonosulfates and metal
peroxides. Bleach activators, also known as peracid precursors, can be included with
the peroxygen compounds. Examples of activators include tetraacetyl ethylenediamine
(TAED), nonanoyloxy benzene-sulfonate (NOBS), and nonanoylglycolate phenol sulfonate
(NOGPS). NOBS and TAED are disclosed, for example, in U.S. 4,417,934, Chung et al.,
and NOGPS is disclosed, for example, in U.S. 4,778,618, Fong et al., the disclosures
of which are incorporated herein by reference. Peracid bleaches (including monoperacids
and diperacids) may be advantageous in terms of bleaching performance. Suitable peracid
bleaching species include C₈₋₁₂ alkyl peracids, especially perazelaic and diperazelaic
acids, diperoxydodecanedioic acid (DPDDA), and alkyl monoperoxysuccinic acid. Peracid
bleaching species, and a method for their production, are described in U.S. 4,337,213
to Marynowski et al., the disclosure of which is incorporated herein by reference.
The bleach is present in an amount sufficient to provide effective bleaching, e.g.,
from about 0% to 10% by weight active, more preferably from about 0.05% to 5% by weight
active depending on the bleaching species chosen.
[0037] Also suitable are chlorine bleaches which could be preformed and suspended on a substrate,
mitigated or generated
in situ.
Alkali-metal Silicate
[0038] An alkali-metal silicate can be included to provide alkalinity and corrosion resistance.
Preferred is one having the formula:
M₂O(SiO₂)
n
where M represents an alkali-metal and n is between about 1 and 4. Preferred alkali-metal
silicates are sodium, potassium and lithium silicates, with sodium silicate being
the most preferred, and with a preferred n value of 2.0-2.4. A most preferred maximum
value for n is about 3.2 in order to minimize insoluble silicates during storage.
It is further preferred that at least about 10% of the total silicates have an n value
of greater than about 1.6 to impart suitable anticorrosive properties. Examples of
other suitable silicates include sodium or potassium orthosilicates and metasilicates.
As used hereinafter, the term "silicate" will be taken to mean any of these alkali-metal
silicates, individually or combined.
[0039] Mixtures of any of the foregoing alkali-metal silicates are also suitable. The alkali-metal
silicate is present in an amount of from about 0% to 10%, preferably about 2% to 5%.
A minimum of about 1% silicate is preferred to provide adequate corrosion resistance.
A commercially available sodium silicate is sold by the Philadelphia Quartz Corporation
(Valley Forge, PA) under the trademarks RU (as a 47% solution) and D (as a 44.1% solution).
In addition to their anti-corrosive effects, the silicates provide alkalinity and
serve as processing aids to increase particle size of the agglomerates. Sodium silicates
also aid in cleaning, especially on oil and grease stains.
Filler
[0040] The filler is preferably a salt such as sodium chloride, nitrate or sulfate, and
is used to adjust the composition density to achieve desired physical characteristics,
e.g., grain size and flowability. Depending on the filler and the process used, the
filler can also provide surface area for loading of actives. The filler material additionally
assists in solubility under cold water washing conditions. Sodium chloride is preferred
due to its low cost and availability. However, other materials, such as puffed borax,
bentonite clays and inorganic salts such as sodium or potassium sulfate, chloride,
bromide, nitrate, and borate, and organic materials like sugars may also be suitable.
Some water may be deliberately added as a filler. Generally, about 0-30% filler will
be present, preferably about 5-25%.
Co-Builder
[0041] Optionally, any non-phosphate builder material known in the art to be compatible
with the high carbonate formulation herein may be included as a co-builder selected
from the group consisting of silicates, citrates, polymeric polycarboxylic acids such
as polyacrylates and malonic anhydride based co-polymers, zeolites, salts of ethylene
diaminetetraacetic acid and sodium nitrilotriacetate. Silicates at levels above about
10%, and citrates may be added as co-builders. If added, the co-builder should comprise
no more than about 30% of the total weight of the composition, and preferably no more
than about 20%. zeolites are preferred as optional co-builders since they perform
well when used in a non-encrustation promoting amount. A non-encrustation promoting
amount is that amount which will not contribute to or encourage the encrustation formation
when present in a detergent formulation and in the presence of water hardness ions.
[0042] Zeolite A is available, for example, from the PQ Corp., Valley Forge, PA, under the
trademark VALFOR 100. Zeolite A typically includes about 21% moisture.
Adjuncts
[0043] While the alkali-metal carbonate is generally sufficient to keep the wash pH range
within the desired limits, it may be desirable to adjust the pH of the wash water
by including an electrolyte/buffer. Generally, these are alkali-metal inorganic acid
salts, hydroxides or oxides. It may also be suitable to use such materials as aluminates
and organic materials, such as gluconates, citrates, succinates, maleates, and their
alkali metal salts. The wash pH range should be maintained between about 8.0 to 13.0,
more preferably about 9.0 to 12.0. If an electrolyte/buffer is needed, sodium hydroxide
is preferred, as it does not interact adversely with any other ingredients and is
very cost effective. The amount of electrolyte/buffer added solely for purposes of
buffering can vary from about 0% to 10%.
[0044] In the standard composition, minor additions can be included in the present invention.
These include dyes, such as Monastral blue and anthraquinone dyes (such as those described
in Zielske, U.S. 4,661,293 and U.S. 4,746,461). Pigments, which are also suitable
colorants, can be selected, without limitation, from titanium dioxide, ultramarine
blue (see also, Chang et al., U.S. 4,708,816), and colored aluminosilicates. Fluorescent
whitening agents are other desirable adjuncts. These include the stilbene,styrene
and styrene, and naphthalene derivatives, which upon being impinged by ultraviolet
light, emit or fluorescent light in a visible wavelength. These fluorescent whitener
agents or brighteners are useful for improving the appearance of fabrics which have
become dingy through repeated soilings and washings. Preferred fluorescent whitener
agents are TINOPAL 5BM-GX and TINOPAL AMS, both from Ciba Geigy A.G., (Tom River,
NJ) and PHORWITE RKH, from Mobay Chemicals (Union, NJ).
[0045] Enzymes, particularly hydrolases such as lipases, proteases and amylases, are useful
additives in the compositions herein. Suitable commercial sources include ESPERASE
and SAVINASE, both trademarked products of Novo Industries (Danbury, CT). Generally,
very low levels of enzymes are needed, i.e. from about 0.1% to 1.0% by weight. Fragrances
are also desirable adjuncts in these compositions. The total composition minors will
range from 0% to about 5%. Anti-redeposition agents, such as carboxymethyl-cellulose,
are potentially desirable. Foam boosters, such as appropriate anionic surfactants,
may be appropriate for inclusion herein. Also, in the case of excess foaming resulting
from the use of certain surfactants, anti-foaming agents, such as alkylated polysiloxanes,
e.g., dimethylpolysiloxane, would be desirable. Water may be present as free water
or as water of hydration of the inorganic salts such as sodium carbonate. The detergent
composition is prepared by a process which yields a dry, free-flowing granular mixture,
for example agglomeration or spray drying. However, the compositions herein are not
limited to such forms, and may also be formulated in other dry forms, such as tablets
or beads, or may be formulated as pastes, gels or liquids. An example formulation
is shown below as Example A.

EXPERIMENTAL
[0046] To assess effectiveness of the compositions herein in reducing encrustation deposition,
compounds of this invention were tested for their effectiveness at reducing encrustation
in beaker studies. The compounds and results are given in the following table.
Procedure
[0047] The turbidity measurement comprises measuring percent transmittance using a dipping
probe and colorimeter. The probe is placed in deionized water and the percent transmittance
(%T.) is set to 100%. The detergent is predissolved in 50 ml of water, then added
to 950 ml of water containing hardness ions as [Ca²⁺]/[Mg²⁺] = 3/1 molar ratio. The
final solution hardness was 300 ppm. Percent transmittance is continuously plotted
and measured vs time. Results are presented as time before the onset of calcium precipitation
(t
m) as determined by an abrupt change in the slope of a graph of %T vs time. The longer
the t
m, the more effective the crystal growth inhibitor. Ideally, with the crystal growth
inhibitor type compounds, the t
m should be longer than the wash cycle, i.e., about 12-15 minutes in the case of washing
conditions in the United States. In practice, a t
m of greater than about 10, preferably 12 minutes, provides commercially-acceptable
results, as calcium precipitation will still be inhibited to a degree sufficient to
avoid consumer preception thereof.
[0048] Simultaneously with the %T measurement, each container of detergent sample has immersed
therein a 3.5 x 4 inch 100% cotton swatch, trimmed to 1.0 grams. Slits approximately
3 inches long were made about 0.25 inch apart for better circulation in the test container.
After washing for 10 minutes, the swatch is rinsed twice with 2 L deionized water,
and placed in a flask containing 25 ml of water and 10 ml of 1.2M HCl to dissolve
the CaCO₃. Fifteen ml of a standard NH₄OH hardness buffer and a Calmagite indicator
are then added and the solution is titrated with standardized EDTA. Results are reported
as mg CaCO₃ per gram of fabric (swatch). Preferably, this value should be below about
4 mg/g, most preferably below about 2 mg/g.
[0049] The preferred level of calcium carbonate deposits per gram of fabric can be achieved
without necessarily extending the t
m value. Although it is understood that this invention is not bound by theory, it is
believed that precipitation modifiers will have little or no effect or may actually
shorten the t
m value and still provide low levels of fabric encrustation. Crystal growth inhibitors,
on the other hand, will extend the t
m value. The presence of either of these compound types in a high carbonate non-phosphate
built detergent has been found to result in lower levels of encrustation on the fabric
surface.

Multicycle Wash Study
[0050] To assess effectiveness of the compositions herein in reducing encrustation deposition,
100% terry cloth washcloths were washed for multiple cycles, under the given wash
conditions. A base detergent composition consisting of 61% Na₂CO₃, 11.0% surfactant,
5.0% sodium silicate and 5.0% sodium perborate were used. The organic dicarboxylic
acid compound was added to the base composition in the amounts indicated in each case
as exemplified in Table II. About 3/4 cup (125 gm/use) of detergent and about 68 l
of wash water was used for each washload.

[0051] Table II shows that substoichiometric levels of the present encrustation preventative
system utilizing an organic dicarboxylic acid of this invention yielded less calcium
residue (as ash) than the base detergent composition at two different treatment levels.
With the observed results for the inhibition of calcium carbonate deposition, an organic
dicarboxylic acid according to this invention could be a direct replacement for polyacrylate
which is known for its anti-precipitation nature. Furthermore, the organic dicarboxylic
acid and water-soluble salts and anhydrides thereof should be more biodegradable than
polyacrylates.
1. A non-phosphate fabric cleaning composition characterised in that it comprises:
(a) a building effective amount of an alkali metal carbonate detergent builder; and
(b) a fabric encrustation preventing amount of an encrustation preventing system,
including a substoichiometric amount of an organic dicarboxylic acid, a water-soluble
salt, an anhydride or mixtures thereof, having the formula:

wherein
R represents 2,1-pyridenyl, 2,4-pyridenyl, 2,6-pyridenyl, 1,2-phenylene, 1,1-phenylene
or

wherein R′ and R˝ independently represent H, -OH or C₁-C₄ alkyl or R′ and R˝ taken
together represent oxygen; n represents 0 or an integer of from 1 to 3; m represents
0, 1 or 2 when R′ is -OH; and M₁ and M₂ independently represent sodium, potassium,
lithium and ammonium.
2. A non-encrustation fabric cleaning composition characterised in that it consists essentially
of:
(a) a building effective amount of an alkali metal carbonate from about 20 to about
80 weight percent;
(b) from about 1 to about 10 percent of a sodium silicate having a ratio of SiO₂/M₂O
of from about 1:1 to about 4:1, wherein M represents an alkali metal;
(c) a sub-stoichiometric amount of an organic dicarboxylic acid, a water-soluble salt
or anhydride and mixtures thereof as defined in claim 1 with the exception that M₁
and M₂ may also independently represent hydrogen;
(d) a detersive cleaning-effective amount of a surfactant selected from anionic, non-ionic,
cationic, amphoteric surfactants and mixtures thereof; and
(e) a bleach effective amount of a bleaching species.
3. A composition as claimed in claim 1 or claim 2 wherein the amount of alkali metal
carbonate builder is from about 20 to about 80 weight percent, preferably from about
30 to about 70 weight percent.
4. A composition as claimed in any of claims 1 to 3 wherein the amount of organic dicarboxylic
acid, water-soluble salt or anhydride thereof is from about 1 to about 20 weight percent.
5. A composition as claimed in any of claims 1 to 4 wherein it includes a detersive cleaning-effective
amount of a surfactant selected from anionic, non-ionic, cationic, amphoteric surfactants
and mixtures thereof, preferably selected from alkyl sulfates, primary and secondary
alkyl sulfonates, linear alkyl aryl sulfonates, alkyl ether sulfates, alkoxylated
aliphatic alcohols, alkoxylated alkyl phenols, copolymers of C₁-C₄ alkylene oxides
and mixtures thereof.
6. A composition as claimed in any of claims 1 to 5 wherein it includes a bleaching effective
amount of a bleaching species.
7. A composition as claimed in any of claims 1 to 6 wherein it includes a non-encrustation
promoting amount of co-builder selected from silicates, citrates, polymeric polycarboxylic
acids, salts or ethylene diamine tetraacetic acid and sodium nitrilotriacetate, and,
preferably, Zeolites.
8. A composition as claimed in any of claims 1 to 7 wherein it includes from about 1
to about 10 percent of an alkali metal silicate.
9. A composition as claimed in any of claims 1 to 8 wherein the alkali metal carbonate
is sodium carbonate; and the organic dicarboxylic acid or water-soluble salt is selected
from phthalic acid, isophthalic acid, 2,4-pyridine dicarboxylic acid, 2,6-pyridine
dicarboxylic acid, 2,3-pyridine dicarboxylic acid, malonic acid, hydroxy malonic acid,
ketomalonic acid, methyl malonic acid, succinic acid, adipic acid, hydroxy succinic
acid and tartaric acid.
10. A composition as claimed in any of claims 1 to 8 wherein the organic dicarboxylic
acid is selected from 2,6-pyridine dicarboxylic acid, ketomalonic acid and hydroxyalonic
acid.
11. A method for reducing water causing precipitation and deposition on fabric characterised
in that it comprises contacting the fabric with a cleaning effective amount of an
aqueous solution of a composition as claimed in any of claims 1 to 10.