[0001] Use of peroxycarboxylic acid-containing suspensions as bleaching compositions, novel
bleaching compositions and bleaching compositions in the packaged form
[0002] The invention relates to the use as pourable bleaching composition of a suspension
in water comprising a peroxycarboxylic acid derived from a dicarboxylic acid containing
8 to 13 carbon atoms.
[0003] Such use is known from British Patent Specification GB 1 535 804. It describes liquid
bleach compositions having a viscosity of from 200 to 100 000 mPa.s and containing
a peroxide, a thickening agent and water. They are suitable for use in washing machines
and automatic clothes dryers.
[0004] The advantages to using liquid bleaching compositions over solid bleaching compositions
are that in their preparation there is no need for cost- increasing shaping steps,
such as drying and granulating, and the fabrics to be treated are rapidly and evenly
bleached, so that high concentrations of the bleaching agent in places can be satisfactorily
avoided.
[0005] To the bleaching compositions of GB 1 535 804, at least as far as they are pourable
(see below), there is the disadvantage that they are not physically stable, which
after prolonged storage results in phase-separated products with a thick bottom layer
which is difficult to disperse or homogenize, as a result of which said advantage
of even distribution over the fabric to be cleaned may partly be eliminated again.
[0006] The present bleaching composition does not show this drawback.
[0007] The invention relates to the use of the above type, characterized in that the bleaching
composition also comprises an alkali metal salt of an alkyl benzene sulphonic acid.
[0008] An additional advantage to the present composition is that, provided that the proportions
of the constituents to be used are properly chosen, it is protected from hazards due
to spilling and drying up, as a result of which solid peroxide particles are formed.
Of peroxides in the solid state it is known that they are exposed to explosion, shock
and abrasion hazards. But in the event of spilling and drying up of properly chosen
present suspensions solid peroxide particles will form that are provided with a coating
such that they are desensitized. The pourable compositions disclosed in GB 1 535 8θ4
are not protected in that way, the amount of thickening agent required for these compositions
being so small that in the event of spilling and drying up solid particles are formed
that are insufficiently desensitized. From experiments it has moreover been found
that this drawback cannot be eliminated by the addition to these suspensions of well-known
desensitizing agents such as sodium sulphate, because the properties of these suspensions
will be even further deteriorated then.
[0009] It should be noted that the present suspensions, containing a peroxycarboxylic acid
and an alkali metal salt of an alkyl benzene sulphonic acid, are disclosed in US 4
126 573. Said patent specification, however, relates to solid, granular bleaching
compositions and the present suspensions are merely applied for the preparations of
these solid compositions by drying, which is in the light apparently of what is mentioned
in the introductory part of US 4 126 573 (column 1, lines 17-20), namely that the
liquid bleaching compositions containing peroxyacid materials as the active bleaching
agent have the tendency to diminish in bleaching effectiveness over prolonged storage
periods.
[0010] Therefore, in view of US 4 126 573, the use of the present suspensions as bleaching
composition is not at all obvious. For, if the peroxycarboxylic acid is finely dispersed
in the water, the chance of decomposition during storage is great. Moreover, from
experiments it has been found that such decomposition occurs in the case of a great
many anionic and nonionic emulsifiers. It has been found, however, that the presence
of an alkali metal salt of an alkyl benzene sulphonic acid as emulsifier has no or
- hardly any detrimental effect on the active oxygen content of the composition.
[0011] The composition according to the invention is physically stable, i.e. after storage
for 6 weeks at 20°C the peroxycarboxylic acid is well dispersed and the suspension
does not display any phase-separation. If precipitation takes place at all, the homogeneity
of the dispersion can be readily restored by gently shaking it.
[0012] Moreover, the composition according to the invention is chemically stable, i.e. after
storage for 2 weeks at 40°C it still has the same or practically the same active oxygen
content.
[0013] The composition according to the invention is pourable, by which is to be understood
that at 20°C the composition has a viscosity between 1 and 1200 mPa.s, preferably
between 50 and 500 mPa.s (Brookfield rotational viscometer [RV type], 20 rpm).
[0014] The invention also relates to those bleaching compositions that are new as such and
to the present bleaching compositions in the packaged form.
[0015] The bleaching component in the present composition consists of a peroxycarboxylic
acid derived from a dicarboxylic acid containing 8 to 13 carbon atoms. Such peroxycarboxylic
acids are not, or hardly soluble in water (solubility less than 1% by weight in water
at 20°C).
[0016] Also mixtures of these acids may be used.
[0017] It is preferred that the present composition should contain diperoxy dicarboxylic
acids, such as 1,12-diperoxydodecanedioic acid, 1,13-diperoxy- tridecanedioic acid
or suitable mixtures thereof.
[0018] The preparation of these acids is effected in a known manner by reacting the corresponding
dicarboxylic acids with hydrogen peroxide in the presence of sulphuric acid.
[0019] Generally, the composition according to the invention contains peroxycarboxylic acid
in an amount such that the active oxygen content of the composition is between 0,1
and 4%, preferably between 0,1 and 3%.
[0020] The present composition must contain an alkali metal salt of an alkyl benzene sulphonic
acid. The alkyl group may be branched or linear and contains 9 to 22 carbon atoms,
preferably 9 to 15 carbon atoms, more particularly 11 to 13 carbon atoms. As examples
of these alkyl benzene sulphonates may be mentioned sodium undecyl benzene sulphonate,
sodium dodecyl benzene sulphonate and sodium tridecyl benzene sulphonate. Also mixtures
of these sulphonates may be used.
[0021] It is preferred that the composition according to the invention should contain sodium
dodecyl benzene sulphonate.
[0022] The alkali metal salt of an alkyl benzene sulphonic acid should be used in an amount
such that the composition is pourable and physically stable. Generally, the composition
will contain alkali metal salt of an alkyl benzene sulphonic acid in an amount of
0,5 to 15% by weight, and preferably 2 to 10% by weight, calculated on the weight
of the composition. Use of amounts less than 0,5% by weight will result in compositions
that have insufficient physical stability; use of amounts higher than 15% by weight
will result in obtaining viscous compositions that are no longer pourable.
[0023] The alkali metal salts of alkyl benzene sulphonic acids commonly used in actual practice
as emulsifier are so-called technical products in which as impurity an inorganic salt
such as sodium sulphate is contained. Although these technical products can very well
be used for preparing the present compositions, a preferred embodiment consists in
that also particular inorganic salts are added. It has been found that adding sodium
sulphate, potassium sulphate or mixtures thereof has a favourable effect on the physical
stability of the compositions, i.e. if there appears to be any precipitation at all
upon using a technical emulsifier alone, it can entirely be stopped by the additional
use of said inorganic salts. It has also been found that when use is made of said
inorganic salts, compositions with the same properties can be prepared that contain
less emulsifier than when no use is made of these inorganic salts. This last- mentioned
embodiment is preferred in actual practice because of the considerably lower cost
price of the inorganic salts as compared with that of the emulsifier to be used. A
preferred inorganic salt is sodium sulphate.
[0024] The amount of inorganic salt to be used will partly be dependent on the amount of
inorganic salt originating from the emulsifier as impurity and should be such that
the bleaching composition is pourable and physically stable. Generally, the bleaching
composition according to the invention will contain inorganic salt, including the
inorganic salt originating from the emulsifier, in an amount of 0,01 to 20% by weight,
preferably 2 to 10% by weight, calculated on the weight of the composition.
[0025] The composition according to the invention may still contain other additives, as
examples of which may be mentioned:
- thickening agents; examples thereof are described in GB 1 535 804. Thickeners can
be used in maximum amounts such that the composition remains pourable;
- sequestering agents, which serve to bind any metal ions present that may accelerate
the decomposition of peroxides. Examples of sequestering agents are ethylene diamine
tetra acetate, sodium pyrophosphate, phosphoric acid, dipicolinic acid and hydroxy
ethylidene diphosphonic acid. They may be used in amounts of 0,01 to 1% by weight,
calculated on the weight of the composition;
- builders, such as polycarboxylates, and finally optical brighteners, perfumes and
organic solvents.
[0026] The present bleaching compositions may very effectively be used in the pre-bleaching
treatment of dirty washing at low temperature (say, about 30°C). In the treatment
of dirty washing with the usually applied heavy and light duty detergents they are
also very suitable to be separately added to the wash liquor. Their effect is at least
equivalent to that of the bleaching compositions disclosed in GB 1 535 804.
[0027] The compositions according to the invention may be prepared by adding the peroxycarboxylic
acid, with stirring, to an acidified mixture (preferably pH 3,5-4,5) of water, alkyl
benzene sulphonate and any other additives. The peroxycarboxylic acid may be used
in the form of powder (primary particle size 1-100 microns) or in the form of wet
filter cake, as obtained after the peroxycarboxylic acid preparation from the corresponding
dicarboxylic acid and hydrogen peroxide. If necessary, the pH of the composition is
finally set to a particularly desired value, which should be in the acid range, use
being made of, for instance, aqueous sodium hydroxide or hydrochloric acid. It is
preferred that the pH should not be higher than 5. Higher values would have a detrimental
effect on the chemical stability of the composition. A pH lower than 2, however, should
also be avoided. For, due to dilution with water of such composition the resulting
insufficiently high final pH would cause the metal parts of the washing machine in
which it is used to be subject to corrosion. Particularly preferred are compositions
having a pH of 3,5-4,5, more particularly 3,9-4,1.
[0028] The invention will be further described in the following examples. All percentages
are by weight.
Example 1
[0029] Compositions as mentioned in Table 1 were prepared. Compositions 1-6 are according
to the invention. The pH values of these compositions were in the range of 3,5 to
4,5.Composition 7 is according to GB 1 535 804.
[0030]

Of each composition a sample was stored for the purpose of evaluating the chemical
stability. After 2 weeks at 40°C all samples had retained their active oxygen content.
[0031] Moreover, of each composition a sample was stored for the purpose of assessing the
physical stability. After 6 weeks at 20°C samples of the compositions 1,2,4,5, and
6 did not display any phase-separation or precipitation phenomena. Although the sample
of composition 3 had precipitated, no thick bottom layer had formed and the original
homogeneity of the dispersion could be restored by gentle shaking. But the sample
of composition 7 had precipitated and a thick bottom layer had formed (phase-separated)
which could not very well be re-dispersed.
[0032] For the purpose of assessing the differences in safeguarding against the hazards
resulting from spilling and drying up between the compositions according to the invention
on the one hand and a composition according to GB 1 535 804 on the other, samples
of compositions 2,3 and 7 were evaporated to dryness by means of an air stream at
25° - 30°C, after which the material thus obtained was subjected to a Pressure Vessel
Test. This test is described in Vervoer Gevaarlijke stoffen, 23 December 1980, Aanhangsel
Al bij bijlage A, pp. 907,908, 915: Staatsuitgeverij. In this test 10 grammes of the
material to be tested are heated by a standardized gas flame in a pressure vessel
fitted with a bursting disk set to 6 bar. In the side wall of the pressure vessel
is a blow-off opening with variable diameter.
[0033] The test procedure implies that such a blow-off opening is found that after decomposition
(explosion, combustion) of the peroxide, the bursting disk is still just intact. The
smaller the admissible opening, the safer the formulation. The admissible opening
(in mm) is given as PVT value. The PVT values found for the material from composition
2 were less than 1 mm, from composition 3 less than 1 mm, and from composition 7 they
were 6 mm. (The PVT value for pure diperoxydodecanedioic acid is 7 mm).
Example 2
[0034] In this example the effect is given of different anionic and nonionic emulsifiers
on the chemical stability of peroxycarboxylic acid suspensions.
[0035] Suspensions were prepared from diperoxydodecanedioic acid (11,65 g of wet filter
cake with an active oxygen content of 5,1%), hydroxyethylidene diphosphonic acid (Dequest
2010
*; 0,25 g), emulsifier and water; the pH of the suspensions was 3,9-4,1.
[0036] The nature of the emulsifiers and the amounts thereof as well as the amounts of water
are given in the table below. The data on the chemical stability of the suspensions,
i.e. the active oxygen content of the suspensions after storage at 40°C, are mentioned
in the lower part of the table.
[0037]

The results in the table show that emulsifiers other than alkyl benzene sulphonate
have a detrimental effect on the chemical stability of peroxycarboxylic acid-containing
suspensions.
[0038] It should be added that suspension 1 is not a composition according to the invention;
it contains about 30% of emulsifier and has a viscosity of 1975 mPa.s. It has been
found that the effect of emulsifiers on the chemical stability of peroxycarboxylic
acid compositions can very well be established when they are used in relatively high
concentrations.
1. Use as pourable bleaching composition of a suspension in water comprising a peroxycarboxylic
acid derived from a dicarboxylic acid containing 8 to 13 carbon atoms, characterized
in that the bleaching composition also comprises an alkali metal salt of an alkyl
benzene sulphonic acid.
2. Use according to claim 1, characterized in that the alkyl group of the alkali metal
salt of an alkyl benzene sulphonic acid contains 9 to 15 carbon atoms.
3. Use according to claim 1, characterized in that the alkali metal salt of an alkyl
benzene sulphonic acid is sodium dodecyl benzene sulphonate.
4. Use according to claim 1, characterized in that the alkali metal salt of an alkyl
benzene sulphonic acid is used in an amount of 0,5 to 15% by weight, calculated on
the weight of the bleaching composition.
5. Use according to claim 1, characterized in that the bleaching composition also
comprises sodium sulphate, potassium sulphate or a mixture thereof.
6. Use according to claim 5, characterized in that the sodium sulphate, potassium
sulphate or mixture thereof is used in an amount of 0,01 to 20% by weight, calculated
on the weight of the bleaching composition.
7. A pourable, aqueous bleaching composition comprising a suspended peroxycarboxylic
acid derived from a dicarboxylic acid containing 8 to 13 carbon atoms, characterized
in that the bleaching composition also comprises an alkali metal salt of an alkyl
benzene sulphonic acid in an amount of 0,5 to 15% by weight and sodium sulphate, potassium
sulphate or a mixture thereof in an amount of 0,01 to 20% by weight, said amounts
being calculated on the weight of the composition.
8. A pourable, aqueous bleaching composition according to claim 7, characterized in
that the peroxycarboxylic acid is 1,12-diperoxydodecanedioic acid and the alkyl group
of the alkali metal salt of an alkyl benzene sulphonic acid contains 9 to 15 carbon
atoms.
9. A packaged bleaching composition, the bleaching composition being of the type described
in any one of the preceding claims