Title of Invention

LUNDRY DETERGENT COMPOSITIONS CONTAINING POLYMERS

Abstract Hydrophobically modified vinyl pyrrolidone polymers which are copolymers having a vinyl pyrrolidone backbone and pendant hydrophobic side chains are useful in laundry detergent compositions to improve detergency and/or antiredeposition. The pendant hydrophobic side chains comprise alkyl chains containing from 4 to 20 carbon atoms and may be linked to the backbone via an ester linkage.
Full Text C4277
FORM - 2
THE PATENTS ACT, 1970 (39 of 1970)
&
The Patents Rules, 2003
COMPLETE SPECIFICATION
(See Section 10 and Rule 13)
LAUNDRY DETERGENT COMPOSITIONS CONTAINING POLYMERS
HINDUSTAN LEVER LIMITED, a company incorporated under the Indian Companies Act, 1913 and having its registered office at Hindustan Lever House, 165/166, Backbay Reclamation, Mumbai -400 020, Maharashtra, India
The following specification particularly describes the invention and the
manner in which it is.to be-perfefmed-. - ——.-


WO 2004/055147

PCT/EP2003/012823


TECHNICAL FIELD 5
The present invention relates to laundry detergent compositions containing certain vinyl pyrrolidone copolymers. The compositions exhibit improved detergency on oily and clay soils and reduced soil redeposition during the L0 wash.
BACKGROUND AND PRIOR ART
/ 15 Polyvinyl pyrrolidone (PVP) and some related polymers are
known ingredients of laundry detergent compositions,
providing the benefit of reduced dye transfer between
fabrics in a mixed load.
20 Laundry detergent compositions containing PVP as a dye transfer inhibitor are disclosed, for example, in VJO 92 18597A and WO 95 27028A (Procter & Gamble) .
GB 1 354 498 (Unilever) discloses laundry detergent 25 compositions containing vinyl pyrrolidone/vinyl acetate
(PVP/VA) random copolymers as antiredeposition agents. PVP itself is stated to be ineffective.
Other vinyl pyrrolidone copolymers are known for cosmetic 30 and agricultural applications.

WO 2004/055147 PCT/EP2003/012823

DEFINITION OF THE INVENTION
In a first aspect, the present invention provides a laundry detergent composition comprising an organic surfactant, and 5 a hydrophobically modified vinyl pyrrolidone polymer which is a copolymer having a vinyl pyrrolidone backbone and pendant hydrophobic side chains comprising alkyl chains containing from 4 to 20 carbon atoms, the polymer being present in an amount effective to improve detergency and/or 10 antiredeposition.
In a second aspect, the invention provides the use of a hydrophobically modified vinyl pyrrolidone polymer to " 15 improve the detergency and/or antiredeposition of a laundry detergent composition.
The hydrophobically modified vinyl pyrrolidone polymer

20
The polymer used in the detergent compositions of the invention is a polyvinyl pyrrolidone modified by the inclusion of hydrophobic units as pendant side chains. The polymer is a copolymer of vinyl pyrrolidone (VP), providing 25 the polymer backbone, and a hydrophobic monomer.
Vinyl pyrrolidone has the formula

0
30

WO 2004/055147

PCT/EP2003/012823

- 3 -
The hydrophobic side chains preferably comprise alkyl chains containing from 4 to 20 carbon atoms.
First preferred embodiment
According to a first preferred embodiment of the invention, the polymer is an alkylated vinyl pyrrolidone polymer wherein the alkyl chains contain from 4 to 20 carbon atoms.
In this embodiment of the invention, the hydrophobic side chains are derived from a hydrophobic comonomer which is an olefin containing from 4 to 20 carbon atoms.
Preferably the polymer contains from 10 to 90 mole% of vinyl pyrrolidone (VP) units and- from 10 to 90 mole% of hydrophobic comonomer units.
Suitable polymers are commercially available from International Specialty Products (ISP) as the Ganex " (Trade Mark), Antaron (Trade Mark) and Agrimer (Trade Mark) series. They may be prepared by chemical modification of PVP with long-chain alpha-olefins. Examples are shown in the Table below.

Polymer trade name Alkyl chain Comonomer (olefin) Mole ratio VP:olefin Physical " form
Agrimer AL-10 Ganex P904LC Antaron P904 C4 Butene 90:10 Water-soluble powder
Ganex V216 Antaron V216 C16 Hexadecene 20:80 Water-insoluble wax
Ganex V516 Antaron V51S C16 Hexadecene 50:50 Water-insoluble wax

WO 2004/055147

PCT/EP2003/012823

- 4 -
Thes-a polymers are marketed for use in cosmetic and personal
care compositions, and for agricultural purposes as ingredients in crop treatment compositions.
5
Second preferred embodiment
According to a second preferred embodiment of the invention, the hydrophobically modified vinyl pyrrolidone polymer has" 10 pendant hydrophobic side chains which are alkyl chains having from 4 to 20 carbon atoms linked to the vinyl pyrrolidone backbone by an ester linkage.
The hydrophobic monomer precursor of the side chains is 15 preferably a vinyl ester of the general formula I:
R1 - CO - 0 - CH » CH2 (I)
1 wherein R is a linear or branched alkyl group having from 4
20 to 16 carbon atoms.
• In the general formula I," R is preferably a linear or
branched alkyl group having from 6 to 10 carbon atoms.
l , 25 More preferably, R is a group of the formula II
R2 - CH - (II)
I
R3 30

WO 2004/055147

PCT/EP2003/012823

- 5
whereinR2- is a linear alkyl group having from 2 to 8 carbon
3 , atoms and R is a methyl or ethyl group.
Most preferably, the hydrophobic comonomer of the formula I is vinyl 2-ethylhexanoate:
10

15

The polymer preferably contains from 90 to 99.5 wt% of vinyl pyrrolidone monomer units and from 0.5 to 10 wt% of vinyl 2-ethyl hexanoate monomer units.
Copolymers of vinyl pyrrolidone and vinyl 2-ethylhexanoate have the general formula III


20
25

WO 2004/055147

PCT/EP2003/012823

- 6 -
Preparation of the polymers having an ester linkage
These polymers may be prepared by free radical polymerisation.
5
A process suitable for preparing these polymers is disclosed in US 5 319 041 (Zhong et al) which describes the synthesis of copolymers of vinylpyrrolidone and vinyl acetate. An alternative process is disclosed in US 5 122 582
L0 (Porthoff-Karl).
The laundry detergent composition
L5 In the detergent composition of the invention, the polymer is present in an amount sufficient to enhance detergency and/or antiredeposition. Suitably the polymer is present in an amount of from from 0.5 to 5 wt%, preferably from 1 to 4 wt%.
20
The detergent composition may suitably comprise:
(a) from 5 to 60 wt%, preferably from 10 to 40 wt%, of
organic surfactant,
(b) optionally from 5 to 80 wt%, preferably from 10 to
25 60 wt%, of detergency builder,
(c) from 0.5 to 5 wt%, preferably from 1 to 4 wt%, of the
hydrophobically modified vinyl pyrrolidone polymer,
(d) optionally other detergent ingredients to 100 wt%.
30

WO 2004/055147

PCT/EP2003/012823


The pH "of the detergent composition is suitably in the range of from 7.0 to 11.0, preferably 7.5 to 10.5. During the wash in dilute form the pH of the detergent composition is from 7 to 11, preferably from 8.0 to 10.5. 5
The organic surfactant
The compositions of the invention may contain any organic 10 surfactants (detergent-active compounds) suitable for incorporation into laundry detergent compositions.
Detergent-active compounds (surfactants) may be chosen from soap and non-soap anionic, cationic, nonionic, amphoteric
15 and zwitterionic detergent-active compounds, and mixtures thereof. Many suitable detergent-active compounds are 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. The preferred
20 detergent-active compounds that can be used are soaps and synthetic non-soap anionic and nonionic compounds. The total amount of surfactant present is suitably within the range of from 5 to 60 wt%, preferably from 5 to 40 w.t%.
25 Anionic surfactants are well-known to those skilled in the" art. Examples include alkylbenzene sulphonates, particularly linear alkylbenzene sulphonates having an alkyl
chain length of C8-C15; primary and secondary
alkylsulphates, particularly C8-C20 primary alkyl sulphates; 30 alkyl ether sulphates; olefin sulphonates; alkyl xylene

WO 2004/055147

PCT/EP2003/012823

- 8 -
sulphonates; dialkyl sulphosuccinates; and fatty acid ester sulphonates. Sodium salts are generally preferred. Nonionic surfactants that may be used include the primary
and secondary alcohol ethoxylates, especially the C8-C20
5 aliphatic alcohols ethoxylated with an average of from 1 to
20 moles of ethylene oxide per mole of alcohol, and more
especially the C10-C15 primary and secondary aliphatic
alcohols ethoxylated with an average of from 1 to 10 moles of ethylene oxide per mole of alcohol. Non-ethoxylated 10 nonionic surfactants include alkylpolyglycosides, glycerol monoethers, and polyhydroxyamides (glucamide).
Cationic surfactants that may be used include quaternary
+ — ammonium salts of the general formula R1R2R3R4N X wherein
15 the R groups are long or short hydrocarbyl chains, typically alkyl, hydroxyalkyl or ethoxylated alkyl groups, and X is a
solubilising anion (for example, compounds in which Ri is a C8-C22 alkyl group, preferably a Cs-Cio or C12-C14 alkyl group, R2 is a methyl group, and R3 and R4, which may be the
20 same or different, are methyl or hydroxyethyl groups); and cationic esters (for example, choline, esters) .
According to a preferred embodiment of the invention, the composition comprises a sulphonate anionic surfactant. 25 According to an especially preferred.embodiment, the
sulphonate anionic"surfactant comprises linear alkylbenzene sulphonate (LAS).

WO 2004/055147

PCT/EP2003/012823

- 9 -
An especially favourable interaction between LAS and the hydrophobically modified vinyl pyrrolidone polymer has been observed, giving improved primary detergency on difficult oily and particulate soils such as dirty motor oil and mud, 5 and reduced redeposition of soil onto the washload during the wash (sometimes referred to as secondary detergency). Without being bound by theory, it is postulated that the this benefit may be attributed to a reduction in the critical micelle concentration (CMC) of the LAS. 10 Preferably, the compositions contains from 3 to 30 wt%, more preferably from 10 to 25 wt%, of LAS.
The optional detergency builder
15
Preferably, the detergent compositions of the invention also contain one or more detergency builders. The total amount of detergency builder in the compositions may suitably range from 5 to 80 wt%, preferably from 10 to 60 wt%.
20
Preferred builders are alkali metal aluminosilicates, more especially crystalline alkali metal aluminosilicates (zeolites), preferably in sodium salt form.
25 Zeolite builders may suitably be present in a-total amount of from 5 to 60 wt%, preferably from 10 to 50 wt%.
The zeolites may be supplemented by other inorganic builders, for example, amorphous aluminosilicates,. or 30 layered silicates such as SKS-6 ex Clariant.

WO 2004/055147

PCT/EP2003/012823

- 10 -
The zeolites may be supplemented by organic builders, for example, polycarboxylate polymers such as polyacrylates and acrylic/maleic copolymers; monomeric polycarboxylates such as citrates, gluconates, oxydisuccinates, glycerol mono-, 5 di- and trisuccinates, carboxymethyloxysuccinates, carboxymethyloxymalonates, dipicolinates,
hydroxyethyliminodiacetates, alkyl- and alkenylmalonates and succinates; and sulphonated fatty acid salts.
10 Alternatively, the compositions of the invention may contain "phosphate "builders, for example, sodium tripolyphosphate.
Especially preferred organic builders are citrates, suitably used in amounts of from 1 to 30 wt%, preferably from .2 to
15 15 wt%; and acrylic polymers, more especially
acrylic/maleic copolymers, suitably used in amounts of from 0.5 to 15 wt%, preferably from 1 to 10 wt%. Builders, both inorganic and organic, are preferably present in alkali metal salt, especially sodium salt, form.
20
According to a preferred embodiment of the invention, the detergency builder, which is present.in an amount of from 5 . to 80 wt%, preferably from 10 to 60 wt%, is selected from sodium tripolyphosphate, zeolites, sodium carbonate and
25 mixtures thereof.
Other detergent ingredients
30 Detergent compositions according to the invention may also suitably contain a bleach system. Preferably this will

WO 2004/055147

PCT/EP2003/012823

- 11 -
include a peroxy bleach compound, for example, an inorganic persalt or an organic peroxyacid, capable of yielding hydrogen peroxide in aqueous solution. Preferred inorganic persalts are sodium perborate 5 monohydrate and tetrahydrate, and sodium percarbonate, the latter being especially preferred. The sodium percarbonate may have a protective coating against destabilisation by moisture. The peroxy bleach compound is suitably present in an amount of from 5 to 35 wt%, preferably from 10 to 25 wt%.
10
The peroxy bleach compound may be used in conjunction with a bleach activator (bleach precursor) to improve bleaching action at low wash temperatures. The bleach precursor is suitably present in an amount of from 1 to 8 wt%, preferably
15 from 2 to 5 wt%. Preferred bleach precursors are
peroxycarboxylic acid precursors, more especially peracetic acid precursors and peroxybenzoic acid precursors; and peroxycarbonic acid precursors. An especially preferred bleach precursor suitable for use in the present invention
20 is N,N,N*,N"-tetracetyl ethylenediamine (TAED).
A bleach stabiliser (heavy metal sequestrant) may also be present. Suitable bleach stabilisers include ethylenediamine tetraacetate (EDTA), diethylenetriamine 25 pentaacetate (DTPA), ethylenediamine disuccinate (EDDS),
and the polyphosphonates such as the Dequests (Trade Mark), ethylenediamine tetramethylene phosphonate (EDTMP) and diethylenetriamine pentamethylene phosphate (DETPMP).
30 • The compositions of the invention may contain alkali metal/ preferably sodium, carbonate, in order to increase

• WO 2004/055147 PCTVEP2003/012823
- 12 -
detergency and ease processing. Sodium carbonate may suitably be present in amounts ranging from 1 to 60 wt%, preferably from 2 to 40 wt%.
As previously indicated, sodium silicate may also be 5 present. The amount of sodium silicate may suitably range from 0.1 to 5 wt%. Sodium silicate, as previously indicated, is preferably introduced via the second base granule.
(
10 Powder flow may be improved by the incorporation of a small amount of a powder structurant. Examples of powder structurants, some of which may play other roles in the formulation as previously indicated, include, for example, fatty acids (or fatty acid soaps), sugars, acrylate or
15 acrylate/maleate polymers, sodium silicate, and dicarboxylic acids (for example, Solcalan (Trade Mark) DCS ex BASF) . One preferred powder structurant is fatty acid soap, suitably present in an amount of from 1 to 5 wt%.
20 Other materials that may be present in detergent (
compositions of the invention include antiredeposition. agents such as cellulosic polymers; soil release agents; anti-dye-transfer agents; fluorescers; inorganic salts such as sodium sulphate; enzymes (proteases, lipases,
25 amylases, cellulases); dyes; coloured speckles; perfumes; and fabric conditioning compounds. This list is not . intended to be exhaustive.

wo 2004/055147
- 13 -
"Product- form and preparation
The compositions of the invention may be of any suitable physical form, for example, particulates (powders, granules, 5 tablets), liquids, pastes, gels or bars.
According to one especially preferred embodiment of the invention, the detergent composition is in particulate form.
Powders of low to moderate bulk density may be prepared by 10 spray-drying a slurry, and optionally postdosing (dry-mixing) further ingredients. "Concentrated" or "compact" powders may be prepared by mixing and granulating processes, for example, using a high-speed mixer/granulator, or other non-tower processes. 15
Tablets may be prepared by compacting powders, especially "concentrated" powders.
Also preferred are liquid detergent compositions, which may 20 be prepared by admixing the essential and optional
ingredients in any desired order to provide compositions containing the ingredients in the requisite concentrations.
25 Incorporation of the hydrophobically modified vinyl pyrrolidone polymer
The polymers may be incorporated at any suitable stage in the manufacture of the compositions of the invention. 30

WO 2004/055147

PCT/EP2003/012823

- 14 -
For-exampley in the manufacture of spray-dried particulate compositions, polymer in powder or solution (preferably aqueous) form may be incorporated in the slurry- For non-tower particulates, polymer powder or solution may be easily introduced into mixing and granulating apparatus, either alone or in admixture with other solid or liquid ingredients as appropriate.
EXAMPLES
The invention is further illustrated by the following Examples, in which parts and percentages are by weight unless otherwise stated.
EXAMPLES 1 to 4
Preparation of vinyl pyrrolidone/vinyl 2-ethylhexanoate
copolymers
The following copolymers were prepared by free radical.. polymerisation. The preparation was adapted from the process described in US 5 319 041 (Zhong et al).

WO 2004/055147 PCT/EP2003/012823
- 15 -

Example Weight%
vinyl pyrrolidone Weight% 1 vinyl 2-ethyl hexanoate
1 99 1
2 " 98 2
3 96 4
4 92 8
The starting materials used were as follows (* denotes Trade Mark) :

Name Chemical name Supplier Aldrich Function
VP Vinylpyrrolidone
Monomer
V2EH Vinyl 2-ethylhexanoate Aldrich Monomer
Vazo* 67 2,2-azobis(2-methylbutyronitrile) Fluka Initiator
Luperox* 101 2.5-bis(tert-butylperoxy)-2.5-dimethylhexane Aldrich Initiator
Butanol n-Butanol Solvent 1
Experimental procedure
The polymers were prepared using a four-step procedure as described below.

WO 2004/055147

PCT/EP2003/012823

- 16 -
The relative weights of VP and V2EH required were calculated in function of the % of hydrophobic units needed in the final copolymer. For example, the total quantities required to make a 200 g batch of the polymer of Example 1 5 are as follows:

Addition Step/Reagent VP
(g) V2EH
(g) VAZO*67
(g) Luperox*101
(g) Butanol
(g)
20.05-2
60.15 19.8
1 2 3 4- 19.8
59.4 19.8 0.25 0.75 0.0312 0.2688 0.0312 0.2688

Total amounts (g) 99 1 0.3 0.3 102
Four-step process 10
A first mixture was prepared to the following composition:


WO 2004/055147

PCT/EP2003/012823

- 17 -
The monomers were charged under a blanket of nitrogen in a 125 mL four-neck flask equipped with a compressed air stirrer, reflux condenser and thermometer. The components
were stirred for about 10 minutes and heated to 85 C. Then a second mixture having the following composition:

Vazo* 67 89.6% of 0.3% of total weight of monomers (VP + V2EH)
Luperox* 101 8 9.6% of 0.3% of total weight of monomers {VP + V2EH)
Butanol 2 g
was added over a period of 30 minutes,
10
A third mixture of having the following composition:

VP 60% of total weight of VP
V2EH 75% of total weight of V2EH"
Butanol 100% of total weight of VP and V2EH; of third mixture

15

was then gradually added over a period of 40 minutes.
Upon completion of V2EH monomer addition, a fourth mixture having the following -composition:

WO2004/05f

PCT/EP2003/012823

- 18 -

VP 20% of total weight of VP
Butanol 100% of weight of VP of fourth mixture
was added over a period of 15 min.
After the above additions were completed, the temperature
5 was increased to 117 C for 3 hours. The reactor contents
were then cooled to room temperature.
The copolymers were characterised by means of proton NMR spectroscopy and gel permeation chromatography. 10
Example 5
Detergency/antiredeposition performance
15 Detergency and antiredeposition performance of the polymers were evaluated by a small scale wash method, using a laundry detergent composition having the following formulation:

Weight%
Linear al.kylbenzene sulphonate 6.00
Sodium C12-C14 alcohol ethoxy sulphate 3EO 10.50
Nonionic surfactant
.(C12-C14 alcohol ethoxylate, 9E0) 6.60
Sodium citrate dihydrate 3.20
Propylene glycol 4.75
Sorbitol
- 3.25
Sodium borate pentahydrate 2.13
(Water to 100.00)

- 19 -
This formulation has a pH of 7.0. In the doseage 1 g/L and 2 g/L it has a pH of 8.8.
Methodology 5
The polymers were tested for their ability to enhance the removal of oily and clay/sebum soil from white cotton fabric, using an apparatus for simulating a soiling and wash procedure on a small scale. 10
Usijig this apparatus, the fabric was soiled, and subjected to a simulated main wash procedure using wash liquors with and without the polymer according to the invention.
15
The apparatus
The wash apparatus used allows different liquids to be simultaneously contacted with different regions of a single
20 sheet of fabric. The fabric sheet is clamped between an upper and lower block. The fabric sheet is sandwiched between two rubber seals. Both blocks and seals contain an 8 x 12 array of square cavities, which are aligned. When blocks and fabrics are clamped together, liquids placed in
25 individual wells do not leak or bleed through to other wells, due to the pressure applied by the blocks in the regions separating the wells. The liquids are forced to flow back and forth through the fabric by means of a pneumatically actuated thin rubber membrane, which is placed
30 between the fabrics and the lower block. Repeated flexing

- 20 -
of the membrane away from and towards the fabrics results in fluid motion through the fabrics.
Soiling
For the oily soil evaluation, the dry fabric was placed on top of a 96 well polypropylene microtitre plate. Oily soil (5 uL of dirty motor oil (15% weight in toluene)) was dispensed from a pipette, onto the centre of each of the 96 cells on .the cloth. The stained fabrics were allowed to dry at room temperature for 24 hours.
For clay/sebum soiling a standard cotton test cloth (AS9) was used.
Wash
The test fabric was then clamped in the washing apparatus, 200 uL doses of each wash solution were placed in appropriate wells. The liquids flowed through the fabrics
for 20 minutes, at 30 C with a flow cycle time of 1.5
seconds. After 20 minutes, the free liquid in the cells was poured off. The blocks where then separated and the fabric removed, and thoroughly rinsed for 1 minute in 200 mL demineralised water. The fabrics were allowed to dry for.24 hours. Reflectance (AE or AR) was then measured.

WO 2004/055147
- 21 -
Experimental conditions
The experiments were carried out at product doses of 0.1,
0.5 and 1.5 g/L, in water of 3 and 12 FH, the hardness
being made up of three parts calcium to 1 part magnesium. The polymers were dosed separately at levels of 0.05, 0.1 and 0.5 g/1, and there was also a polymer-free control for each set of conditions.
For the tests using oily soil (.dirty motor oil) , the results are "expressed as SRI (soil release index) , where SRI - 100 - AE
For the tests using clay/sebum soil, the results are expressed as AR (image analysis, equivalent to AR at 460 run) .
Results for the polymer of Example 4 Clay/sebum soil

Product
dose
g/L Water Hardness (°F) AR (460 njn) for polymer concentrations of


o ■
(control) 0.05 0.5
0.1 3 4.01 4.13 4.37
0.5 3 3.99 4.36 4.72
1.5 3 4.60 5.44 5.72
0.1 12 3.50 4.00 3.84
0.5 12 3.67 4.01 3.99
1.5 12 3.94 4.36 4.80

- 22 -Oily soil (dirty motor oil)

Averaged results for the polymers of Examples 1-4
The following table shows the results for all four polymers 10 on oily soil (dirty motor oil) averaged over all product
levels (0.1, 0.5 and 1.5 g/1), polymer levels (0.05, 0.1 and
0.5 g/1), and water hardnesses (3 and 12 FH).
The results are expressed as reflectance increases (AR) 15 compared with a control containing no polymer. All results represent a significant difference at 95%.

- 23 -

Polymer of Example Mean AR
1 0.49
2 0.36
3 0.46
4 0.51


We Claim
1. A laundry detergent composition comprising an organic surfactant, and a hydrophobically modified vinyl pyrrolidone polymer which is a copolymer having a vinyl pyrrolidone backbone and pendant hydrophobic side chains comprising alkyl chains containing from 4 to 20 carbon atoms linked to the backbone by an ester linkage the polymer being present in an amount effective to improve detergency and/or antiredeposition.
2. A detergent composition as claimed in claim 1, characterised in that the polymer has pendant hydrophobic side chains derived from olefins containing from 4 to 20 " carbon atoms.
3. A detergent composition as claimed in claim 2, characterised in that the polymer contains from 10 to 90 mole% of vinyl pyrrolidone units and from 10 to 90 mole% of hydrophobic comohomer units.
4. A detergent composition as claimed in claim 3, characterised in that the pendant hydrophobic side chains of the copolymer are derived from a vinyl ester of the general formula I:
R1 - CO - 0 - CH = CH2
wherein R1 is a linear or branched alkyl group having from 4 to 16 carbon atoms.
i
5. A detergent composition as claimed in claim 4,
characterised in that in the general formula I R1 is a



wherein R2 is a linear alkyl group having from 2 to 8 carbon atoms and R3 is a methyl or ethyl group.
A detergent composition as . claimed in claim 5, characterised in that the polymer contains units derived from vinyl 2-ethylhexanoate.
A detergent composition as claimed in claim 6, characterised in that the polymer contains from 90 to 99.5 wt% of vinyl pyrrolidone monomer units and from 0.5 to 10 wt% of virtyl 2-ethylhexanoate monomer units.
A detergent composition as claimed in any preceding claim, characterised in that it contains from 0.5 to 5 wt%, preferably from 1 to 4 wt%, of the hydrophobically modified vinyl pyrrolidone polymer.
A detergent composition as claimed in any preceding claim, characterised in that it comprises:
(a) from 5 to 60 wt%, preferably from 10 to 40 wt%, of organic surfactant,
(b) optionally *from 5 to 80 wt%, preferably from 10 to 60 wt%, of detergency builder,
(c) from 0.5 to 5 wt%, preferably from 1 to 4 wt%, of the hydrophobically modified vinyl pyrrrolidone polymer,
(d) optionally other detergent ingredients to 100 wt%.


10. A detergent composition as claimed in any preceding claim characterised in that it has a pH of from 7.0 to 11.0, preferably 7.5 to 10.5.
11. A detergent composition as claimed in any precediff claim, characterised in that the organic surfactant (a) comprises a sulphonate anionic surfactant.
12. A detergent composition as claimed in claim 11, characterised in that the organic surfactant (a) comprises linear alkylbenzene sulphonate.
13. A detergent composition as claimed in claim 14, characterised in that it contains from 3 to 30 wt%, preferably from 10 to 25 wt%, of linear alkylbenzene sulphonate.
14. A detergent composition as claimed in any preceding claim, characterised in that it comprises from 5 to 80 wt%, preferably from 10 to 60 wt%, of detergency builder selected from sodium tripolyphosphate, zeolites, sodium carbonate and mixtures thereof.

Dated this 1 st day of June 2005.
26

Documents:

00528-mumnp-2005-cancelled pages(23-02-2006).pdf

00528-mumnp-2005-claims(granted)-(20-03-2006).doc

00528-mumnp-2005-claims(granted)-(20-03-2006).pdf

00528-mumnp-2005-correspondence(23-02-2006).pdf

00528-mumnp-2005-correspondence(ipo)-(19-10-2007).pdf

00528-mumnp-2005-form 1(01-06-2006).pdf

00528-mumnp-2005-form 18(13-10-2005).pdf

00528-mumnp-2005-form 2(granted)-(20-03-2006).doc

00528-mumnp-2005-form 2(granted)-(20-03-2006).pdf

00528-mumnp-2005-form 3(01-06-2006).pdf

00528-mumnp-2005-form 5(23-02-2006).pdf

00528-mumnp-2005-power of attorney(23-02-2006).pdf

00528-mumnp-form-pct-ipea-409(01-06-2005).pdf

00528-mumnp-form-pct-isa-210(01-06-2005).pdf

528-MUMNP-2005-CORRESPONDENCE(8-2-2012).pdf


Patent Number 211229
Indian Patent Application Number 528/MUMNP/2005
PG Journal Number 45/2007
Publication Date 09-Nov-2007
Grant Date 19-Oct-2007
Date of Filing 01-Jun-2005
Name of Patentee HINDUSTAN UNILEVER LIMITED
Applicant Address HINDUSTAN LEVER HOUSE 165/166, BACKBAY RECLAMATION, MUMBAI 400020
Inventors:
# Inventor's Name Inventor's Address
1 MACNAB DONNA C/O UNILEVER R&D PORT SUNLIGHT, QUARRY ROAD EAST, BEBINGTON, WIRRAL, MERSEYSIDE, CH63 3JW
2 SORET CATHERINE MARIE-JOSEPH SIMONE OXFORED UNIVERSITY, PHYSICAL AND THEORETICAL CHEMISTRY LABORATORY, SOUTH PARKS ROAD, OXFORD, OXFORDSHIRE, OX1 QZ
3 THOMAS ROBERT KEMEYS OXFORED UNIVERSITY, PHYSICAL AND THEORETICAL CHEMISTRY LABORATORY, SOUTH PARKS ROAD, OXFORD, OXFORDSHIRE, OX1 QZ
4 WAL ALBERT VAN DER UNILEVER TECHNOLOGY VENTURES ADVISORY COMPANY LLC, 812 ANACAPA STREET, SUITE A, SANTA BARBARA, CALIFORNIA 93101
PCT International Classification Number C11D3/37
PCT International Application Number PCT/EP03/12823
PCT International Filing date 2003-11-12
PCT Conventions:
# PCT Application Number Date of Convention Priority Country
1 0229146.6 2002-12-13 U.K.