[0001] This invention relates to a light duty detergent powder composition designed especially
for washing fine garments and synthetic fabrics.
[0002] Fine garments and synthetic and coloured fabrics require careful treatment and yet
need to be cleansed and washed like any other wash goods. The washing process, and
therefore any composition used in such a process, should not damage the fabric fibres,
should not bleach any dyes or pigments in the fabrics and should not cause loss of
brightness by the deposition of insoluble material onto the fabric surface. At the
same time effective soil removal is required. Furthermore a detergent powder that
feels soft and non-gritty in the hands would likely have a better consumer appeal
for being identified with mildness to fine garments.
[0003] French patent specification 2 237 960 (Unilever NV) describes a detergent composition
which in addition to a detergent active material contains an alkyl hydroxyalkyl cellulose
and a maleic acid copolymer. Compositions are disclosed therein which contain no bleach
and are thus suitable for the treatment of fine garments. European patent specification
EP 54 325-B (Unilever NV et al) describes compositions which contain a mixture of
sodium carboxymethyl cellulose, a linear polymer polycarboxylate and a cellulose ether.
The specifically exemplified compositions recommend the presence of 5% sodium silicate.
[0004] It is an object of this invention to provide a non-gritty, soft-feeling light duty
detergent powder composition especially designed for effective washing of fine garments
and synthetic fabrics and yet is exceptionally mild to colour and fabric caring.
[0005] According to the invention there is provided a bleach-free powdered detergent composition
for washing fine garments and synthetic and coloured fabrics, comprising:
(i) from 10% to 35% by weight of an organic surface active agent selected from anionic
surfactants, nonionic surfactants and mixtures thereof;
(ii) from 5% to 60% of a detergency builder; and
(iii)from 1% to 15% of a polymer mixture containing (a) an alkali metal carboxymethyl
cellulose having from 0.5 to 0.9 carboxymethyl ether groups per anhydrose unit and
(b) an alkylhydroxyalkyl cellulose derivative having a total number of substituent
groups per glucose unit of between 1.5 and 3.0; characterised in that the composition
contains no sodium silicate and the polymer mixture additionally contains (c) a polycarboxylate
polymer selected from compounds having the empirical formula:

wherein X is O or -CH₂-, Y is a comonomer or mixture of co-monomers, R¹ and R² are
bleach stable polymer end groups, R³ is H, OH or C₁ to C₄ alkyl, M is a water-soluble
cation, p is from 0 to 2 and n is at least 10, and mixtures thereof.
[0006] The compositions of the present invention are essentially free of bleach and sodium
silicate. Impurities in other ingredients may accidentally introduce these materials,
especially the sodium silicate. Such impurities will generally only be present in
small amounts in the overall composition, up to about 0.5% by weight.
[0007] The individual components of the polymer mixture system are known in the art. However
the use of this particular mixture in a high active, non-bleaching and sodium silicate-free
detergent composition provides for the desired beneficial properties of an attractive
light duty detergent powder composition destined for the fine wash.
[0008] Polymer (a) - A well-known representative of this polymer is sodium carboxymethylcellulose
as available on the market, which has been used as soil-suspending and anti-redeposition
agent in fabric washing detergent compositions.
[0009] Polymer (b) - To be of use in accordance with the invention, the total number of
substituent groups per glucose unit of the cellulose derivative should be between
about 1.5 and about 3.0, preferably between about 2.0 and about 3.0. There should
be at least about 1.0, preferably from about 1.0 to about 2.5, and particularly preferably
from about 1.5 to about 2.1, alkyl groups per glucose unit; and at least about 0.1,
preferably from about 0.2 to about 1.5, and particularly preferably from about 0.5
to 1.5, hydroxyalkyl groups per glucose unit. The alkyl groups should contain from
1 to 4, and preferably from 1 to 3, carbon atoms, and the hydroxyalkyl groups should
contain from 2 to 4, preferably from 2 to 3, carbon atoms. Particularly preferred
alkyl groups are methyl and ethyl, and the preferred hydroxyalkyl groups are hydroxyethyl
and hydroxypropyl. Propyl, butyl and hydroxybutyl groups may also be used. When the
alkyl group is methyl it is preferred that the hydroxyalkyl group be hydroxypropyl,
and when the alkyl group is ethyl it is preferred that the hydroxyalkyl group be hydroxyethyl,
although it will be appreciated that other combinations of alkyl and hydroxyalkyl
groups may be used if desired. Particularly preferred cellulose derivatives for use
in accordance with the invention are methyl hydroxypropyl celluloses having from 1.7
to 2.1 methyl groups per glucose unit and from 0.8 to 1.0 hydroxypropyl groups per
glucose unit, and ethyl hydroxyethyl celluloses having from 1.5 to 1.6 ethyl groups
per glucose unit and from 0.5 to 0.6 hydroxyethyl groups per glucose unit.
[0010] Many of these cellulose derivatives are available commercially, for example under
the Trade name of Modocoll®, supplied by the Mo och Domsjo Company, and others may
readily be prepared by simple chemical procedures. For instance, a methyl hydroxypropyl
cellulose derivative may be prepared by reacting the cellulose with dimethylsulphate
and then with propylene oxide (or vice versa: if one substituent is to be present
in a greater amount than the other, it is preferabe that the major substituent is
applied first), and an ethyl hydroxyethyl cellulose may be prepared by reacting the
cellulose with ethylene oxide and then with ethyl chloride.
[0011] The polycarboxylate polymers (c) are disclosed and further characterised in EP-A-137
669, the most important members of which are:
(i) those belonging to the class of copolymeric polycarboxylates which, formally at
least, are formed from an unsaturated polycarboxylic acid such as maleic acid, citraconic
acid, itaconic acid and metaconic acid as first monomer, and an unsaturated monocarboxylic
acid such as acrylic acid or an alpha-C₁-C₄-alkyl acrylic acid as second monomer.
Preferred copolymers of this class are copolymers of maleic acid (anhydride) and (meth)acrylic
acid, as disclosed in EP-B-25 551 and GB Patent 1 596 756.
(ii) those belonging to the class of poly (alpha-hydroxyacrlyates);
(iii)those belonging to the class of polyacetal carboxylates or acetal polycarboxylates;
and
(iv) those belonging to the class of homopolymeric polyacrylates.
[0012] Any polymer of these classes can be chosen as polymer (c) in the polymer mixture,
either alone or as mixture, though preference is given to polymers of the classes
(i) and (iv).
[0013] These polymers should preferably be present in the composition at a total level of
from 1.5% to 10% by weight in proportions of about 0.2-2% by weight of polymer (a),
about 0.1-3% by weight of polymer (b) and about 0.5-10%, most preferably about 1-5%
by weight of polymer (c).
[0014] The detergent composition of the invention contains at least one detergent-active
material, preferably at a level of 15% to 25% by weight. This material may be anionic
or nonionic in nature, but mixtures of anionic and nonionic materials are preferred.
[0015] The anionic detergent-active material can be a soap or a non-soap (synthetic) anionic
material. Anionic detergent-active materials 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.
[0016] Synthetic anionic detergent-active materials useful in the present invention are
water-soluble alkali metal salts of organic sulphates and sulphonates having alkyl
radicals 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 (C₈-C₁₈) alcohols produced for example from tallow or
coconut oil, sodium and potassium alkyl (C₉-C₂₀) benzene sulphonates, particularly
sodium linear secondary alkyl (C₁₀-C₁₅) 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
monoglyceride sulphates and sulphonates; sodium and potassium salts of sulphuric acid
esters of higher (C₈-C₁₈) 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 amines of methyl taurine; alkane monosulphonates such
as those derived by reacting alpha-olefines ((C₈-C₂₀) with sodium bisulphite and those
derived from reacting paraffins with SO₂ and Cl₂ and then hydrolysing with a base
to produce a random sulphonate; sodium and potassium salts of fatty acid ester sulphonates;
water-soluble salts of dialkyl esters of sulphosuccinic acid; and olefin sulphonates,
which term is used to describe the material made by reacting olefins, particularly
C₁₀-C₂₀ alpha-olefins, with SO₃ and then neutralising and hydrolysing the reaction
product. The preferred anionic detergent compounds are sodium (C₁₁-C₁₅) alkyl benzene
sulphonates and sodium (C₁₆-C₁₈) alkyl sulphates.
[0017] Mixtures of anionic compounds may also be used, preferably mixtures of synthetic
anionic surfactants and alkalimetal soaps.
[0018] Examples of suitable nonionic surfactants include:
1. The polyethylene oxide condensates of alkyl phenol, e.g. the condensation products
of alkyl phenols having an alkyl group containing from 6 to 12 carbon atoms in either
a straight chain or branched chain configuration, with ethylene oxide, the said ethylene
oxide being present in amounts equal to 3 to 30, preferably 5 to 14 moles of ethylene
oxide per mole of alkyl phenol. The alkyl substituent in such compounds may be derived,
for example, from polymerised propylene, di-isobutylene, octene and nonene. Other
examples include dodecylphenol condensed with 9 moles of ethylene oxide per mole of
phenol; dinonylphenol condensed with 11 moles of ethylene oxide per mole of phenol;
nonylphenol and di-isooctylphenol condensed with 13 moles of ethylene oxide.
2. The condensation product of primary or secondary aliphatic alcohols having from
8 to 24 carbon atoms, in either straight chain or branched chain configuration, with
from 2 to about 40 moles, preferably 2 to about 9 moles of ethylene oxide per mole
of alcohol. Preferably, the aliphatic alcohol comprises between 9 and 18 carbon atoms
and is ethoxylated with between 2 and 9, desirably between 3 and 8 moles of ethylene
oxide per mole of aliphatic alcohol. The preferred surfactants are prepared from primary
alcohols which are either linear (such as those derived from natural fats or prepared
by the Ziegler process from ethylene, e.g. myristyl, cetyl, stearyl alcohols), or
partly branched such as the Lutensols, Dobanols and Neodols which have about 25% 2-methyl
branching (Lutensol being a Trade Name of BASF, Dobanol and Neodol being Trade Names
of Shell), or Synperonics, which are understood to have about 50% 2-methyl branching
(Synperonic is a Trade Name of ICI) or the primary alcohols having more than 50% branched
structure sold under the Trade Name Lial by Liquichimica. Specific examples of nonionic
surfactants falling within the scope of the invention include Dobanol 45-4, Eobanol
45-7, Dobanol 45-9, Dobonal 91-2.5, Dobanol 91-3, Dobanol 91-4, Dobanol 91-6, Dobanol
91-8, Dobanol 23-6.5, Synperonic 6, Synperonic 14, the condensation products of coconut
alcohol with an average of between 5 and 12 moles of ethylene oxide per mole of alcohol,
the coconut alkyl portion having from 10 to 14 carbon atoms, and the condensation
products of tallow alcohol with an average of between 7 and 12 moles of ethylene oxide
per mole of alcohol, the tallow portion comprising essentially between 16 and 22 carbon
atoms. Secondary linear alkyl ethoxylates are also suitable in the present compositions,
especially those ethoxylates of the Tergitol series having from about 9 to 15 carbon
atoms in the alkyl group and up to about 11, especially from about 3 to 9, ethoxy
residues per molecule.
[0019] The compounds formed by condensing ethylene oxide with a hydrophobic base formed
by the condensation of propylene oxide with propylene glycol. The molecular weight
of the hydrophobic portion generally falls in the range of about 1500 to 1800. Such
synthetic nonionic detergents are available on the market under the Trade Name of
"Pluronic", supplied by Wyandotte Chemicals Corporation.
[0020] The mixing ratio of anionic to nonionic materials is not very critical and can be
varied as desired by the skilled artisan. However, preference here is given to ratios
within the range of 6:1 to 1:2, preferably from 5:1 to 1:1.
[0021] The detergent compositions according to the invention also contain a detergency builder,
which can be an inorganic builder or an organic builder, in an amount generally within
the range of from about 5% to about 60%, preferably from 15% to 50% by weight.
[0022] Examples of phosphorus-containing inorganic detergency builders include the water-soluble
salts, especially alkali metal pyrophosphates, orthophosphates and polyphosphates.
Specific examples of inorganic phosphate builders include sodium and potassium tripolyphosphates,
phosphates and hexametaphosphates.
[0023] Examples of non-phosporus-containing inorganic detergency builders, when present,
include water-soluble alkali metal carbonate, bicarbonates, and crystalline and amorphous
alumino silicates. Specific examples include sodium carbonate (with or without calcite
seeds), potassium carbonate, sodium and potassium bicarbonates.
[0024] Examples of organic detergency builders, when present, include the alkali metal,
ammonium and substituted ammonium polyacetates, carboxylates, polycarboxylates, polyacetal
carboxylates and polyhydroxysulphonates. Specific examples inlcude sodium, potassium,
lithium, ammonium and substituted ammonium salts of ethylenediaminetetraacetic acid,
nitrilotriacetic acid, oxydisuccinic acid, melitic acid, benzene polycarboxylic acid
and citric acid.
[0025] Sodium silicate is usually relied upon in detergent compositions to provide alkalinity.
In the compositions of this invention the desired alkalinity can be obtained by the
use of water-soluble alkaline builder materials. Alkali metal carbonates and their
mixtures with alkali metal phosphates are especially suitable.
[0026] In use, the detergent compositions according to the invention will preferably show
a pH of between 9.0 and 10.5.
[0027] It should be appreciated that the detergent composition according to the invention
may further contain any of the conventional additives in amounts in which such materials
are normally employed in fabric-washing detergent compositions and which serve to
further improve the laundering characteristics and/or add aesthetic appeal to the
compositions. Examples of these additives include lather boosters, anti-foaming agents,
non-silicate alkaline materials fabric-softening agents, corrosion inhibitors, inorganic
salts, sequestering agents, colouring agents and perfumes, so long as these additives
do not adversely influence the basic objective of the invention. Enzymes such as proteolytic,
lipolytic and amylolytic enzymes are preferably incorporated to effect stain removal
by bioaction.
[0028] Though in a preferred embodiment, the invention omits the use of fluorescent agents
or optical bleaching agents, as these additives could change the hue of the original
fabric colours, their presence in very small amounts up to about 0.02% by weight is
generally desirable for aesthetic reasons in giving brightness to the powder appearance.
[0029] The detergent composition of the invention is generally manufactured and presented
in the form of a particulate powder, which includes the form of granules. Detergent
powder compositions according to the invention can be prepared using any of the conventional
manufacturing techniques commonly used or proposed for the preparation of fabric-washing
detergent powder compositions. These include slurry-making of the basic ingredients
followed by spray-drying or spray-cooling and subsequent dry-dosing of sensitive ingredients
not suitable for incorporation prior to the drying or heating step. Other conventional
techniques, such as noodling, granulation, dry-mixing, and mixing by fluidisation
in a fluidised bed, may be utilised as and when necessary and desired. Such techniques
are familiar to those skilled in the art of detergent powder composition manufacture
and require no further explanation as being essential to the invention.
[0030] The absence of silicate gives a snowy aspect of the powder and favours quick solubility
of the product without insolubles.
[0031] Whereas polymer (c), such as polyacrylates or acrylic acid/maleic acid copolymers,
aids in giving structure to the powder, the combined use thereof with polymer (a)
e.g. sodium carboxymethyl cellulose, and polymer (b) e.g. ethyl hydroxyethyl cellulose,
results in a further enhancement of the anti-redeposition properties of the composition;
with improved wettability of synthetic fibres being observed.
[0032] The invention will now be further described with reference to the following non-limiting
examples.
Example 1
[0033] The following detergent composition was prepared by spray-drying the basic ingredients
and dry-mixing the enzyme and anti-foaming agent.

[0034] The product obtained was a light powder of bulk density 0.40 g/cc having an appealing
white snowy appearance and a soft feel in the hands with very good solubility and
detergency properties.
[0035] When two similar products are compared, one containing 6.0% sodium silicate and one
in which the silicate was absent (the balance being made up by sodium sulphate), it
was found that the composition containing the silicate left a residue of insoluble
material when dissolved in water at 20°C, which residue was 3 times greater than that
left by the silicate-free composition.
1. A bleach-free powdered detergent composition for washing fine garments and synthetic
and coloured fabrics, comprising:
(i) from 10% to 35% by weight of an organic surface active agent selected from anionic
surfactants, nonionic surfactants and mixtures thereof;
(ii) from 5% to 60% of a detergency builder; and
(iii)from 1% to 15% of a polymer mixture containing (a) an alkali metal carboxymethyl
cellulose having from 0.5 to 0.9 carboxymethyl ether groups per anhydrose unit and
(b) an alkylhydroxyalkyl cellulose derivative having a total numter of substituent
groups per glucose unit of between 1.5 and 3.0;
characterised in that the composition contains no sodium silicate and the polymer
mixture additionally contains (c) a polycarboxylate polymer selected from compounds
having the empirical formula:

wherein X is O or -CH₂-, Y is a comonomer or mixture of co-monomers, R¹ and R² are
bleach stable polymer end groups, R³ is H, OH or C₁ to C₄ alkyl, M is a water-soluble
cation, p is from 0 to 2 and n is at least 10, and mixtures thereof.
2. A composition according to Claim 1 in which polymer (c) is a copolymer of an unsaturated
polycarboxylic acid and an unsaturated monocarboxylic acid.
3. A composition according to Claim 1, in which the polymer (c) is a homopolymeric
polyacrylate.
4. A composition according to Claim 1, in which the polymer mixture contains from
0.2 to 2% by weight of polymer (a), from 0.1 to 3% of polymer (b) and from 0.5 to
10% of polymer (c).
5. A composition according to Claim 1, in which the detergency builder comprises an
alkali metal carbonate or a mixture thereof with an alkali metal phosphate.
6. A composition according to Claim 1, which is free of fluorescent agents and optical
bleaching agents.