[0001] The present invention relates to a particulate, soap-containing detergent composition.
[0002] Such compositions are well known in the art; they are either based on soap as the
sole detergent-active material, or they contain soap in admixture with non-soap synthetic
detergents, such as anionic, nonionic, cationic, zwitterionic or amphoteric synthetic
detergents and mixtures thereof.
[0003] Normally, the soap component used in these compositions is a soap derived from palm
oil, tallow, coconut oil and the like, as well as mixtures thereof. However, part
of these soaps, especially of sodium coconut soap, does not effectively contribute
to the water-softening and detergency of the soap component; the major part of sodium
coconut soap serves only a solubilization purpose, but does not itself contribute
effectively to the overall detergency of the soap component.
[0004] It has now been found that if the soap component in particulate, soap-based detergent
compositions is substantially free (i.e. less than 5%, preferably less than 3%) of
a sodium soap of a C
12 or C
14 saturated fatty acid, and contains a certain level (hereafter to be more precisely
defined) of a sodium soap of linoleic acid, the overall detergency performance of
such soap-based compositions is_ improved, as well as the solubility of the soap component.
The present invention therefore in its broadest sense relates to a particulate, soap-containing
detergent composition in which the soap is substantially free from sodium soaps of
C
12 or C
14 saturated fatty acids, and in which the soap is or comprises a sodium linoleate.
[0005] The soap component in the detergent composition may consist solely of sodium linoleate,
or it may contain, besides the sodium linoleate, a soap of C
16-C
24 monounsaturated fatty acid, such as e.g. sodium oleate. The sodium linoleate improves
the solubility of such soap blends, These soap blends may further contain up to
30, e.g. up to 25% by weight of a sodium soap of saturated C
16-C
24 fatty acids, without impairment of the benefits of the invention.
[0006] The soap component therefore consists of 10-100% sodium linoleate, 0-90% sodium soap
of C
16-C
24 monounsaturated fatty acids, and 0-30% of C
16-C
24 saturated fatty acids, the total of the three types of soao being 100%.
[0007] The soap component may be prepared by admixing the separately prepared soap constituents,
or by neutralizing a mixture of the respective fatty acids. Such a mixture may be
made up separately, or it may be obtained from a natural source which contains these
respective fatty acids. Such sources are e.g. soapstock fatty acids, tall oil fatty
acids, and several natural fats and oils, such asgroundnut oil, grapeseed oil,.mustard
oil, maize oil, soybean oil, chufa oil, rapeseed oil, sesame oil, sunflower oil etc.
In particular, sodium soaps of rapeseed oil, tall oil fatty acids, soybean and sunflower
oil are preferred sources of the required fatty acids to obtain the maximum benefit
of the invention. The soap component of the invention is used in a particulate composition
in an amount of 0.5-99% by weight. The higher part of this range, i.e. from 30-70%
relates to compositions wherein the soap is used as the sole detergent active material,
e.g. in soap powders, together with adjuvants such as builders, bleaching agents,
alkaline salts, sequestering agents and the like. The range from 70-99% relates to
compositions primarily consisting of the soap, e.g.in flake, ribbon, noodle and similar
discrete-shaped form, in powder form, etc, with minor amounts of adjuvants.
[0008] The lower range of 1-30% relates to compositions in which the soap is used together
with other, synthetic detergent active materials in particulate detergent compositions.
[0009] Such compositions normally include from about 2% to about 30%, preferably about 10%
to about 25%, by weight of a synthetic anionic, nonionic, cationic, amphoteric or
zwitterionic detergent compound or mixture thereof. Many suitable detergent compounds
are commercially available and are' fully described in the literature, for example
in "Surface Active Agents and Detergents", Volumes I and II, by Schwartz, Perry and
Berch.
[0010] The preferred detergent compounds which can be used are synthetic anionic and nonionic
compounds. The former are usually watersoluble alkali metal salts of organic sulphates
and sulphonates having alkyl groups containing from about 8 to about 22 carbon atoms,
the term alkyl being used to include the alkyl portion of higher acyl radicals. Examples
of suitable synthetic anionic detergent compounds are sodium and potassium alkyl sulphates,
especially those obtained by sulphating higher (C
8-C
18) alcohols produced for example from tallow or coconut oil; sodium and potassium alkyl
(C
9-C
20) benzene sulphonates, particularly sodium linear secondary alkyl (C
10-C
15) benzene sulphonates; sodium alkyl glyceryl ether sulphates, especially those ethers
of the higher alcohols derived from tallow or coconut oil and synthetic alcohols derived
from petroleum; sodium coconut oil fatty acid monoglyceride sulphates and sulphonates;
sulphonated fatty acids and esters thereof; sodium and potassium salts of sulphuric
acid esters of higher (C
9-C
18) fatty alcohol-alkylene oxide, particularly ethylene oxide, reaction products; the
reaction products of fatty acids such as coconut fatty acids esterified with isethionic
acid and neutralised with sodium hydroxide; sodium and potassium salts of fatty acid
amides of methyl taurine; alkane monosulphates such as those derived by reacting alpha-olefins
(C
8-C
20) with sodium bisulphite and those derived by reacting paraffins with S0
2 and C1
2 and then hydrolysing with a base to produce a random sulphonate; and olefin sulphonates,
which term is used to describe the material made by reacting olefins, particularly
C
10-C
20 alpha-olefins, with SO
3 and then neutralising and hydrolysing the reaction product. The preferred anionic
detergent compounds are sodium (C
11-C
15) alkyl benzene sulphonates and sodium (C
16-C
18) alkyl sulphates.
[0011] Examples of suitable nonionic detergent compounds which may be used include in particular
the reaction products of alkylene oxides, usually ethylene oxide, with alkyl (C
6-C
22) phenols, generally 5 to 25 E0, i.e. 5 to 25 units of ethylene oxide per molecule;
the condensation products of aliphatic (C
8-C
18) primary or secondary linear or branched alcohols with ethylene oxide, generally
6 to 30 E0, and products made by condensation of ethylene oxide with the reaction
products of propylene oxide and ethylene diamine. Other so-called nonionic detergent
compounds include long chain tertiary amine oxides, long chain tertiary phosphine
oxides and dialkyl sulphoxides.
[0012] Mixtures of detergent compounds, for example mixed anionic or mixed anionic (anionic-including,soaps)and
nonionic compounds may be used in the detergent compositions, particularly in the
latter case to provide controlled low sudsing properties. This is beneficial for compositions
intended for use in suds-intolerant automatic washing machines.
[0013] Amounts of amphoteric or zwitterionic detergent compounds can also be used in the
compositions of the invention instead of part or all of the nonionics, such as sulphobetaines,
amidobetaines, alkylamino acids and the like. Cationics may also be used, such as
cetyltrimethylammoniumbromide.
[0014] Apart from the detergent compounds, the detergent compositions of the invention can
contain any of the conventional additives in the amounts in which such materials are
normally employed in fabric-washing detergent compositions. Examples of these additives
include lather boosters such as alkanolamides, particularly the monoethanolamides
derived from palm kernel fatty acids and coconut fatty acids, lather depressants such
as alkyl phosphates and silicones, anti-redeposition agents such as sodium carboxymethylcellulose
and polyvinyl pyrrolidone, oxygen-releasing bleaching agents such as sodium perborate
and sodium percarbonate, per-acid bleach precursors such as TAED, chlorine-releasing
bleaching agents such as trichloroisocyanuric acid and alkali metal salts of dichloroisocyanuric
acid, fabric- softening agents, inorganic salts such as sodium sulphate, sodium carbonate
and magnesium silicate, and, usually present in very minor amounts, fluorescent agents,
perfumes, enzymes such as proteas.es and amylases, germicides, colourants, and scum
dispersants.
[0015] It is also possible to include one or more anti-deposition agents in the detergent
compositions of the invention, to decrease any tendency to form inorganic deposits
on washed fabrics. The amount of any such anti-deposition agents is normally from
about 0.1% to about 5% by weight, preferably from about 0.2% to about 2% by weight
of the compositions. The preferred anti-deposition agents are homo- and co-polymers
of acrylic acid or substituted acrylic acids, such as sodium polyacrylate, the sodium
salt of copolymethylacrylamide/acrylic acid and sodium poly-alpha-hydroxyacrylate,
salts of copolymers of maleic anhydride with ethylene, vinylmethylether or styrene,
especially 1:1 cooolymers, and optionally with partial e'ster- ification of the carboxyl
groups especially in the case of the styrene-maleic anhydride copolymers. Such copolymers
preferably have relatively low molecular weights, e.g. in the range of about 5,000
to 50,000. Other anti-deposition agents include the sodium salts of polymaleic acid
and polyitaconic acid, phosphate esters of ethylated aliphatic alcohols, polyethylene
glycol phosphate esters, and certain phosphonates such as sodium ethane-l-hydroxy-l,l-diphosphonate,
sodium ethylene diamine tetramethylene phosphonate, and sodium 2-phosphonobutane tricarboxylate.
Mixtures of organic phosphonic acids or substituted acrylic acids or their salts with
protective colloids such as gelatin as described in our Netherlands application 7602082
may also be used. The most preferred anti-deposition agent is sodium polyacrylate
having a MW of about 10,000 to 50,000, for example about 27,000.
[0016] The compositions of the invention may also contain builder salts, such as alkali
metal ortho-, pyro- and polyphosphates, alkali metal carbonates, carboxymethyloxysuccinates,
alkali metal citrates in amounts of up to 50%. Where it is desired to increase detergency
whilst using particularly low levels of phosphate builders, so as to achieve low or
no phosphorus contents in the detergent compositions, non-phosphate detergency builders
such as amine carboxylates, e.g. sodium nitrilotriacetate, sodium aluminosilicate
ion-exchange materials, sodium carbonate and sodium citrate are preferred. However,
builder materials are not essential and it is a particular benefit of the compositions
of the invention that satisfactory detergency and-water-softening properties can be
achieved with the presence of the particular soap component of the invention.
[0017] It is also possible to include in the compositions for fabric washing purposes an
amount of an alkali metal silicate, particularly sodium ortho-, meta- or preferably
neutral or alkaline silicate. The presence of such alkali metal silicates at levels
of at least about 5%, and preferably from about 15% to about 30% by weight of the
composition, is advantageous in decreasing the corrosion of metal parts in washing
machines, as well as giving processing benefits and generally improved powder properties.
In combination with non-phosphate builders there is the additional benefit of improved
magnesium inactivation. For industrial laundering higher amounts of silicates can
be included, e.g. up to 90% of meta-silicate. Often sodium carbonate can also be included
(up to 50%) as further source of alkalinity in industrial laundering products.
[0018] The compositions of the invention may be prepared by any suitable process for preparing
particulate compositions, such as spray- drying, spray-cooling, dry-mixing, granulation,
flaking, noodling and the like, the soap being added direct or via the slurry.
[0019] The invention will be further illustrated by way of example.
EXAMPLE
[0020] Two soap-based powders were prepared, having the following compositions:
Tests were carried out in a Tergotometer at 80°C, at a water hardness of 26° French
hardness, at 4, 5.5 and 7 g/l product concentration, using three different standard
soiled test-pieces. The following ΔR results were obtained.