Background of the invention
1. Field of the invention
[0001] The invention relates to an aqueous liquid bleaching composition comprising a selected
organic peroxy acid, which composition may be used for the bleaching of fabrics and
hard surfaces.
2. The prior art
[0002] Quite a number of organic peroxy acids have been reported in the literature. These
peroxy materials have begun to assume great commercial importance as bleaches, especially
for fabrics. Many of the more effective organic peroxy acids are solid, substantially
water-insoluble materials. Much of the published art has been directed at devising
means for stably suspending these peroxyacids in water.
[0003] One of the early patents in the area is US 3,996,152 disclosing the suspension of
substantially water-insoluble peroxyacids by non-starch thickening agents such as
Carbopol 94® in an aqueous media at low pH. Suggested as suitable peroxyacid were
diperazelaic, diperbrassylic, dipersebacic and diperisophthalic acids. US Patent 4,017,412
reports similar systems except that starch based thickening agents were employed.
From later investigations it became evident that the thickener type systems mentioned
in the foregoing patents formed gel-like matrices which exhibited instability upon
storage at elevated temperatures.
When formulated at high levels, these thickeners-systems became more stable but then
caused difficulties with pourability.
[0004] US Patent 4,642,198 lists an even more expansive variety of water-insoluble organic
peroxy acids intended for suspension in an aqueous, low pH liquid. Herein was first
disclosed the use of surfactants, both anionic and nonionic, as suspending agents
for the peroxyacid particles.
[0005] The preferred peroxy material was identified as 1,12-diperoxydodecanedioic acid (DPDA)
and this was employed in almost all the examples.
[0006] EP-A-0 176 124 also focusses upon surfactant suspended 1,12-diperoxydodecanedioic
acid in a low pH aqueous liquid. This art informs that surfactants other than alkylbenzene
sulfonate have a detrimental effect upon chemical stability of the suspensions.
[0007] EP-A-0 240 481 seemingly also finds some special significance in the use of alkylbenzene
sulfonate, focusses upon DPDA, and further suggests use of magnesium sulfate as a
suspension aid and peracid stabiliser.
[0008] Other surfactant suspending systems for peroxyacids are disclosed in US Patents 4,824,592
and US 4,828,747. The peroxyacids disclosed herein are of the classes disclosed in
the foregoing patents with preference for DPDA.
[0009] In US Patent 4,822,510 there is suggested to use 4,4'-sulphonyl-bisperoxybenzoic
acid as the solid, water-insoluble peroxyacid.
[0010] The aforementioned art has placed great emphasis upon optimizing the suspending systems
of the liquid bleach to improve stability.
Evidently, there has been little consideration given to improving both stability and
performance altogether.
[0011] Consequently it is an object of the present invention to provide an improved aqueous
liquid bleach composition based upon a solid, substantially water-insoluble organic
peroxy acid having improved stability and performance.
[0012] More specifically, it is an object of the present invention to provide an aqueous
suspension of a solid, substantially water-insoluble organic peroxy acid, which is
chemically and physically stable throughout a wide range of temperatures and which
is moreover highly effective for use in the disinfecting and bleaching of substrates,
e.g. fabrics and hard surfaces.
[0013] These and other objects of the present invention will become apparent as further
details are provided in the subsequent discussion and Examples.
SUMMARY OF THE INVENTION
[0014] An aqueous liquid bleaching composition having a pH of from 1 to 6.5 is herein provided
comprising:
( i) from 1 to 40% by weight of a solid, substantially water-insoluble peroxyacid
having the general formula:

wherein X is H, alkyl chain, a halogen, a carboxyl group in any position on the aromatic
ring, or the same peroxycarboxylic acid group.

in symmetrical position to the first peroxyacid group on the aromatic ring;
R is a straight or branched chain lower alkylene having 1-4 carbon atoms, preferably
- CH₂ -; and
n is between 1-12, preferably 3-8.
( ii) from 2 to 50% by weight of a surfactant; and
(iii) from 1.5 to 30% by weight of an electrolyte.
DETAILED DESCRIPTION OF THE INVENTION
[0015] It has now been found that imidoperoxycarboxylic acids of formula (I) above when
presented as an aqueous suspension comprising a surfactant and electrolyte as hereinbefore
defined at a pH within the range of 1-6.5, preferably from 2-5, are not only extremely
stable both physically and chemically, but also show very effective bleaching and
disinfecting properties already at low temperatures e.g. from ambient to about 40°C,
as compared to similar formulations based on DPDA as the peroxyacid.
[0016] Preferred examples of imidoperoxycarboxylic acids usable in the present invention
are those having the following structures:

of which phthaloylamino peroxy caproic acid (("PAP") of formula (1) is particularly
preferred.
[0017] Amounts of this class of peroxyacids to be used in the compositions of this invention
range from about 1 to about 40% by weight, preferably from about 2 to 30%, optimally
between about 5 and 20% by weight.
[0018] The particle size of the peroxy acid used in this invention is of some importance.
Particles that are too large have been found to readily separate while very small
particle sizes decrease chemical stability. Advantageously the range of particle size
should be from about 10 to 1,000 microns, preferably between 20 and 500 microns, optimally
between 30 and 250 microns.
[0019] Surfactants are required to stably suspend the imidoperoxy carboxylic acid of the
present invention. Suitable for this purpose are anionic, nonionic, cationic, zwitterionic
surfactants and mixtures thereof. However, the preferred system is a mixed anionic
and nonionic detergent combination.
[0020] Nonionic surfactants useful for the present invention may be selected from a wide
category of materials, many of which are outlined in Schwartz, Perry Vol. II, 1958
"Detergents and Surface Agents" and Schick, vol. I, 1967 "Nonionic Surfactants". For
instance, fatty acids, fatty alcohols, fatty amides and alkoxylated derivations thereof
may be usefully employed. Within the alkoxylate category, there is recommended ethylene
oxide and/or propylene oxide condensation products of C₈-C₂₀ linear-or branched-chain
aliphatic carboxylic acids, aliphatic alcohols and alkyl phenols. Especially preferred,
however, are the C₁₂-C₁₈ aliphatic alcohols ethoxylated with an average from about
3 to about 12 moles of ethylene oxide per alcohol molecule. Even more specifically
the C₁₂-C₁₅ alcohols condensed with either an average of 3 or 9 moles ethylene oxide
and the C₁₂-C₁₄ aliphatic alcohols condensed with 7 moles ethylene oxide have been
found to be highly effective.
[0021] Anionic surfactants which may be useful for the present invention can be found listed
in Schwartz, Perry, Vol. II, 1958 "Detergents and Surface Active Agents".
[0022] Examples of anionic materials are water-soluble salts of alkylbenzene sulfonates,
alkyl sulfates, alkyl ether sulfates, diakyl sulfosuccinates, paraffin sulfonates,
α-olefin sulfonates, α- sulfocarboxylates and their esters, alkyl glycerol ether sulfonates,
alkyl phenol polyethoxy ether sulfates, 2-acyloxy-alkane-1-sulfonates, β-alkoxyalkane
sulfonates, secondary alkane sulfonates, and mixtures thereof.
[0023] The cationic detergents which can be used in the present invention include quaternary
ammonium salts which contain at least one alkyl group having from 12 to 20 carbon
atoms.
Although the halide ions are the common anions, other suitable anions include acetate,
phosphate, sulfate, nitrate and the like.
[0024] Specific cationic detergents include distearyl dimethyl ammonium chloride, stearyl
dimethyl benzyl ammonium chloride, stearyl trimethyl ammonium chloride coco dimethyl
benzyl ammonium chloride, dicoco dimethyl ammonium chloride, cetyl pyridinium chloride,
cetyl trimethyl ammonium bromide, stearyl amine salts that are soluble in water such
as stearyl amine acetate and stearyl amine hydrochloride, stearyl dimethyl amine hydrochloride,
distearyl amine hydrochloride, alkyl phenoxyethoxyethyl dimethyl ammonium chloride,
decyl pyridinium bromide, pyridinium chloride derivative of the acetyl amino ethyl
esters of lauric acid, lauryl trimethyl ammonium chloride, decyl amine acetate, lauryl
dimethyl ethyl ammonium chloride, the lactic acid and citric acid and other acid salts
of stearyl-1-amidoimidazoline with methyl chloride, benzyl chloride, chloroacetic
acid and similar compounds, mixtures of the foregoing, and the like.
[0025] Zwitterionic detergents include alkyl-β-iminodipropionate, alkyl-β-aminopripionate,
fatty imidazolines, betaines, and mixtures thereof. Specific examples of such detergents
are 1-coco-5-hydroxyethyl-5-carboxymethyl imidazoline, dodecyl-β-alanine, the inner
salt of 2-trimethylamino lauric acid, and N-dodecyl-N,N-dimethyl amino acetic acid.
[0026] The total surfactant amount in the liquid bleaching composition of the invention
may vary from 2 to 50% by weight, preferably from 5 to 35% by weight, depending on
the purpose of use.
In the case of suspending liquids comprising an anionic and a nonionic surfactant,
the ratio thereof may vary from about 10:1 to 1:10. The term anionic surfactant used
in this context includes the alkali metal soaps of synthetic or natural long-chain
fatty acids having normally from 12 to 20 carbon atoms in the chain.
[0027] Preferred surfactant mixtures usable in the present invention are mixtures of:
i) sodium C₁₀-C₁₈ alkyl benzene sulphonate and an ethyloxylated nonionic surfactant;
ii) Sodium C₁₂-C₁₈ secondary alkane sulphonate and an ethoxylated nonionic surfactant,
[0028] Mixtures including a fatty acid, especially C₁₂-C₁₈ fatty acids, are particularly
preferred.
[0029] The total level of electrolyte(s) present in the composition to provide structuring
may vary from about 1.5 to about 30%, preferably from 2.5 to 25% by weight. Examples
of electrolytes include inorganic compounds such as sodium sulfate and sodium nitrate,
and mixtures thereof.
[0030] Since most commercial surfactants contain metal ion impurities (e.g. iron and copper)
that can catalyze peroxy acid decomposition in the liquid bleaching composition of
the invention, those surfactants are preferred which contain a minimal amount of these
metal ion impurities. The peroxy acid instability results in fact from its limited,
though finite, solubility in the suspending liquid base and it is this part of the
dissolved peroxy acid which reacts with the dissolved metal ions. It has been found
that certain metal ion complexing agents can remove metal ion contaminants from the
composition of the invention and so retard the peroxy acid decomposition and markedly
increase the lifetime of the composition.
[0031] Examples of useful metal ion complexing agents include dipicolinic acid, with or
without a synergistic amount of a water-soluble phosphate salt; dipicolinic acid N-oxide;
picolinic acid; ethylene diamine tetraacetic acid (EDTA) and its salts; various organic
phosphonic acids or phosphonates such as hydroxyethylidenediphosphonic acid (Dequest
2010
R), ethylene diamine tetra-(methylene phosphonic acid), -Dequest 2040- and diethylene
triamine penta-(methylene phosphonic acid)-Dequest
R 2060.
[0032] Other metal complexing agents known in the art may also be useful, the effectiveness
of which may depend strongly on the pH of the final formulation. Generally, and for
most purposes, levels of metal ion complexing agents in the range of from about 10-1000
ppm are already effective to remove the metal ion contaminants.
[0033] In addition to the components discussed above, the liquid bleaching compositions
of the invention may also contain certain optional ingredients in minor amounts. Typical
examples of optional ingredients are suds-controlling agents, such the various silicone
oils, fluorescers, perfumes, coloring agents, abrasives, hydrotropes and antioxidants.
However, any such optional ingredient should only be incorporated if its presence
in the composition does not significantly reduce the chemical and physical stability
of the peroxy acid in the suspending system.
[0034] A particularly preferred optional ingredient is hydrogen peroxide (H₂O₂). It has
been found that hydrogen peroxide, when incorporated in the aqueous liquid bleach
composition of the invention is quite compatible with the imido peroxy carboxylic
acid. Addition of hydrogen peroxide to the present bleach composition serves to provide
an additional benefit of boosting its high temperature (i.e. above 60°C) bleaching
performance.
[0035] Usually and in practice an amount of about 2% to 10% by weight, preferably from 4%
to 6% by weight of hydrogen peroxide in the composition is adequate to achieve the
desired effect.
[0036] Aqueous liquid products encompassed by the invention will have a viscosity in the
range of from about 50 to 20,000 centipoises (0.05 to 20 Pascal seconds) measured
at a shear rate of 21 second-¹ at 25°C. In most cases, however, the products of the
invention will have a viscosity of from about 0.2 to about 12 PaS, preferably between
about 0.5 and 1.5 PaS.
[0037] Also of importance is that the aqueous liquid bleaching compositions of this invention
have an acid pH in the range of from 1 to 6.5, preferably from 2 to 5, particularly
between 3.0 and 4.5.
[0038] The following Examples will more fully illustrate the embodiments of this invention.
All parts, percentages and proportions referred to herein are by weight of the total
composition unless otherwise stated.
Examples I - IV
[0039] The following table shows aqueous liquid bleach formulation within the invention
which are stable and effective.
