Title of Invention	LAUNDRY COMPOSITIONS FOR USE IN A TUMBLE DRYER
Abstract	Laundry treatment process, which comprises tumble drying clothes in the presence of a chelating agent which has one nitrogen atom and at least four carboxylic acid groups per molecule, or a salt thereof.

Full Text

FORM -2 THE PATENTS ACT, 1970 (39 of 1970) COMPLETE SPECIFICATION (See Section 10) LAUNDRY COMPOSITIONS FOR USE IN A TUMBLE DRYER 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 nature of the invention and the manner in which it is to be performed; LAUNDRY COMPOSITIONS FOR USE IN A TUMBLE DRYER Technical Field The present invention relates to improvements to fabric treatment compositions and a process for use of the same. It is particularly concerned with a method and compositions for use with a tumble drier. Background to the Invention Sequestering agents have been used in detergents since ancient times, when materials such as citric and tartaric acid were employed to obtain clear products with good solubility. In particular traces of metals such as ferric iron can cause discoloration of textiles and it has long been known to use sequestering agents, such as oxalic acid, to remove them. In 1937, IG Farbenindustrie introduced the amino-carboxylic acid sequestrants for use in the dyeing industry. It is well known that traces of metals, particularly calcium, magnesium, iron, copper and aluminium are often responsible for faulty dyeing. These impurities can be present in a dye bath because of corrosion from fittings, from the water used or as carry over from a previous process. The difficulties that occur in the dyeing process are due to the sensitivity of the dyestuffs to these trivalent and divalent cations. Dyestuffs form less soluble salts with these metals and this can lead to precipitation. Additionally, many dyestuffs contain complexing groups which complex with metal ions and may lead to changes in the solubility or colour of the dye. This latter point is particularly true with the mordant dyes. Chrome dyes, on the other hand intentionally chelate chromium and the replacement of chromium with iron in the dyestuff leads to a disastrous change of colour. Almost everyone is aware that repeated laundering of clothes will eventually cause most colours to fade or change in tint or hue. Consequently, many products have been marketed under the banner of "colour care". The first of these merely omitted bleach and other components which could damage colours. Later developments have included the incorporation of agents to prevent dye loss or dye transfer. In certain ways, the environment within which laundering processes occur is similar to that in a dyeing bath. Dyed fabric, is. subjected, to a combination of heat and water of variable purity and it is to be expected that the presence of metal ions will cause similar problems to those that occur in dyeing. In recent years, it has been suggested that sequestrants can have benefits in the laundering process. The laundering process comprises a series of unit operations of which several involve the wet treatment of fabrics. These can include pre-soak and pre-treatment processes, as well as the more commonplace washing/rinsing process. Often these washing and rinsing processes are mechanised. Optional processing includes machine-drying either by centrifuge or by the application of heat, as in a so-called "tumble drier". Treatment components can be added at various stages, for example, with detergents being added in the wash and conditioners being added in the rinse. W0 2000/34427 discloses the use of the sequestrant IDS (iminodisuccinic acid) at various stages within the laundry process as part of a non-bleaching detergent composition containing IDS for colour care and stain-removal benefits. US 5686376 discloses the possibility of adding sequestering agents in the rinse to improve colour fidelity. Instances of treatment in the drier are less common. Often, treatment in the drier is restricted to the addition of perfume (from a so-called "drier sheet") although it is also possible to treat fabrics with conditioners/softeners during this operation. US 6107270 discloses dryer-added fabric softener compositions that are said to provide colour and other fabric benefits. Suggested sequestering agents include TPED (Quadrol L), EDDS and NTA. US 6025321 discloses further dryer-added fabric softener composition to provide colour and other fabric benefits, suggesting the same sequestering agents. Persistent staining and colour loss and/or change on fabrics are major issues for many users of domestic detergent compositions. There is therefore an ongoing need to find improved sequestering agents and or the means for delivering them. Brief Description of the Invention We have determined that a particular group of sequestering agents gives an improved colour benefit and indeed even a colour restoration benefit when used in the tumble drier. It t is believed that this is in some way due to the removal of metal ions associated with the fabrics either through staining or through an earlier step in the laundry process. It is believed that treatment with these materials prevents further transition metal ion colour damage and that such treatment can give stain removal benefits in the next wash. The present invention provides a laundry treatment process, which comprises tumble drying clothes in the presence of a chelating agent which has one nitrogen atom and at least four carboxylic acid groups per molecule or a salt thereof. The present invention also provides a laundry treatment composition comprising a chelating agent which has one nitrogen atom and at least four carboxylic acid groups per molecule, or a salt thereof together with instructions to use in the tumble drier. The present invention also provides a laundry drier sheet comprising a substrate and a chelating agent is of the general formula HOOC- (R1 . COOH) R2-NR5-R3 (R4 . COOH) -COOH wherein R1-R5 are each independently, C1-C5 alkyl, hydroxy-alkyl or hydrogen. Detailed Description of the Invention Preferred 1-N 4-COOH chelating agents are disuccinnic acids containing a nitrogen hetero-atom. Preferred materials are amine-bridged. Preferably, the chelating agent is of the general formula: HOOC- (R1.COOH) R2-NRs-R3(R4.COOH)-COOH (1) wherein R1-R5 are each independently, C1-C5 alkyl, hydroxy-alkyl or hydrogen. In this arrangement, two of the carboxylic acid groups are disposed on either side of the bridging nitrogen atom. In a preferred embodiment, R1-R4 in the formula (1) are methylene and R5 is hydrogen. A particularly preferred material is therefore iminodisuccinnic acid or a salt thereof. The structure of which is given below as formula (2) . HOOC-(CH2.COOH) CH-NH-CH(CH2.COOH)-COOH (2) It is envisaged that the corresponding hydroxy acids can also be used. The process can be conducted in the presence of other fabric treatment agents. These are preferably one or more of a fabric softening agents, fabric conditioning agents, perfumes, anti-static agents, dye-transfer inhibiting polymers, dye fixing agents, other sequestrants, chlorine scavenging agents, lubricants, cross-linking polymers, soil release polymers, and optical brightening agents. In its broadest aspect, compositions that embody the present invention can be in the form of a liquid, gel, paste, foam, powder, sheet, film, deformable solid, breakable solid or combination thereof. A particularly preferred form is that of the drier sheet. Preferred sheets are non-woven, and are more preferably embossed. A range of suitable materials are known including a polyester/rayon (50:50 mix) in sheet form. Levels of sequestrant are typically such that the weight of seguestrant is in the range 0.0005-1.0%wt of the weight of cloth being placed in the drier. In order that the invention may be further understood it will be described below with reference to the following non-limiting examples. Examples: The reflectance versus wavelength profile of 1%, Direct Red 80 dyed, unfixed, woven, cotton fabric was measured using the large aperture on a Texicon ICS Spectraflash 500 ™, (excluding the UV below 42 0nm). Sixteen measurements were taken (using 4 cloth thicknesses over the Spectraflash aperture). The Direct Red 80 dyed cotton fabric was obtained from Campbell Hayward Ltd. (Springvale Works, Shawclough Rd. Waterfoot, Rossendale, Lanes. BB4 9JZ) and was not made up into garments. The fabric was then washed twice in demineralised water containing transition metal and water hardness ions at the following concentrations : 1. 1ppm Cu2+: 2 . Oppm Fe3+: 0.12ppm Mn2+: 2. 3ppm Zn2+. The levels selected are quoted in the literature as being representative of the transition metal ion levels found in the main wash for soiled loads(Patent WO9403553). Water hardness was 4°FH Ca2+: 2°FH, Mg2+ Washing was performed in a vertical axis (US) machine (Whirlpool™ Super Capacity Plus Washer) set for a 12min wash on a small load setting. Twc applications of transition metal ions were performed in order to damage the fabric by transition metal ion deposition. This has the effect of changing the hue of the fabric, to give a visible blue tinge. The fabric was dried in a tumble dryer (Whirlpool™ Super Capacity Dryer) after each wash. The change in colour of the "colour-damaged" fabric when treated"with chelating agents, provides a sensitive measure of their efficacy. For these experiments, this fabric was cut into 2 0cm2 swatches and overlooked. The reflectance versus wavelength profile of these swatches was measured using the large aperture on a Texicon ICS Spectraflash 500 ™, (excluding the XJV below 420nm) to obtain a comparative measure of damage compared to the new fabric. Here, 4 measurements were taken per swatch, using 4 cloth thicknesses over the Spectraflash aperture. Five swatches were used per drying experiment. The swatches were rewet using demineralised water, prior to mixing in with a wet ballast load, containing white non-mercerised, desized woven cotton. The ballast had previously been put through a rinse cycle with demineralised water. Examples 1-5 and comparatives; The dose response characteristic of IDS was investigated using the IDS concentrations (% on total weight of fabric in the load), given in table 1 below. . To obtain these results a Miele Novotronic™ T454 tumble dryer was allowed to warm up on "extra dry cotton" heat setting for 5min. A nonwoven, embossed, polyester/rayon (50:50 mix) sheet (95gm"2) was loaded with 62.5g of IDS liquid sequestrant (Iminodisuccinic acid, tetrasodium salt, 40% activity ex. Nippon Shokubai). This corresponds to 1% IDS on weight of fabric for a 2.5kg load. The IDS solution was spread out evenly over the sheet, using a glass rod. The sheet was placed inside the dryer, with the 2.5kg fabric load comprising white, desized, non-mercerised, cotton ballast + five 20x20cm "colour damaged", Direct Red 80, overlocked, cotton test swatches. The load was dried on the extra dry cotton heat setting. Once the load was dry, the test swatches were removed from the tumble dryer and the reflectance versus wavelength profile was measured for each using the large aperture on a Texicon ICS Spectraflash 500 ™, (excluding the UV below 42 0nm). Four measurements were taken per cloth (using 4 cloth thicknesses over the Spectraflash aperture) giving a total of 2 0 readings per wash load. This experiment was repeated for separate wash loads using concentrations of 0.5%, 0.1%, 0.01 and 0.005% IDS on weight of fabric based on a 2.5kg load. N.B. The total volume of IDS solution added onto the sheet was kept constant at 62.5g. The experiment was performed twice for each IDS concentration, giving a total of 40 reflectance readings per concentration. The average reflectance reading at 620nm for each concentration is quoted in Table 1. Comparison of the reflectance profiles showed that the reflectance value at 62 0nm was found to be the most sensitive wavelength for measuring differences in the sequestering capability of the IDS for ions on the fabric surface. The results from the dose response experiment at 620nm are shown below in Table 1. (95% confidence limits were calculated for. the. experiment using the Excel statistical analysis tool.) Table 1 - Dose Response for IDS Example Treatment Mean Reflectance at 620nm Standard Deviation Confidence Limits Comparative A Unwashed 46.56 - Comparative B Damaged 35.99 - Comparative C 0% IDS 37.92 1.70 1.49 1 0.005% IDS 39.84 2.71 1.68 2 0.01% IDS 43.68 2.72 1.69 3 0.1% IDS 49.64 4.21 2.61 4 0.5% IDS 54.98 0.88 0.54 5 1% IDS 53.89 1.86 1.15 1 From these results it can be seen that washing fabric in the presence of the metal ions causes a significant lowering of reflectance at this wavelength (compare comparative A with B). Some of this loss can be recovered by wetting, and drying the fabric with demineralised water (compare comparative B with C). However, it can be seen that the presence of even low levels of IDS causes a significant improvement in the recovery of mean reflectance. Examples 6 and comparatives: A level of 0.01% sequestrant was chosen for the investigation into the relative performances between the sequestrants listed below-. a) TPED (N, N, N", N" tetrakis (2-hydroxy propyl) ethylenediamine: available as Quadrol TM L, 100% activity, ex BASF). b) EDDS (ethylene diamine disuccinic acid tri sodium salt available as Octaquest E30 ™ ex Octel 32,7%) c) NTA (Nitrilotriacetic acid sodium salt monohydrate 99% ex Aldrich) . The method used was the same as that used for examples 1-5. Results are given in table 2 below: Table 2: - Comparison with other sequestrants Example Treatment Mol. Wt. Mean Ref. at 620nm Std. Deviation 95% Conf. Comparative A Unwashed - 46.56 0.16 0.16 Comparative B Damaged - 35.99 0.29 a.28 Comparative C 0% IDS - 37.92 1.70 1.49 6 0.01% IDS 337.1 43.68 2.72 1.69 Comparative D 0.01% EDDS 358 40 3.02 1.87 Comparative E 0,01% TPED 292.42 40 1.70 1.05 Comparative P 0.01% NTA 257 39 3.9 2.42 From these results it can be shown that the IDS sequestrant shows statistically better performance at equivalent weight (0.01%) than the other sequestrants (TPED, EDDS and NTA, comparatives D-F). Example 7 and Comparatives; Woven fabric dyed with 1% Direct Red 8 0 (unfixed) was obtained from Campbell Hayward Ltd. (Springvale Works, Shawclough Rd. Waterfoot, Rossendale, Lancs. BB4 9JZ) The reflectance versus wavelength profile was measured for the new fabric using the large aperture on a Texicon ICS Spectraflash 500 ™, (excluding the UV below 420nm). Sixteen measurements were taken (using 4 cloth thicknesses over the Spectraflash aperture). The red woven fabric was treated with transition metal ions as follows: The fabric was washed twice in demineralised. water containing transition metal and water hardness ions at the following concentrations: l.lppm Cu2+: 2. 0ppm Fe3+: 0.12ppm Mn2+: 2. 3ppm Zn2+. The levels selected are quoted in literature (WO9403553)as being representative of the transition metal ion levels found in the main wash when soiled loads are used. Water hardness was: 4°FH Ca2+: 2°FH Mg2+ Washing was performed in a vertical axis (US) machine (Whirlpool™ Super Capacity Plus Washer) set for a 12min wash on a small load setting. Two applications of transition metal ions were performed in order to damage the fabric by transition metal ion deposition. This has the effect of changing the hue of the fabric, to give a visible blue tinge. The fabric was dried in a tumble dryer (Whirlpool™ Super Capacity Dryer) in between each wash. The change in colour of the "colour-damaged" fabric when treated with chelating agents, provides a sensitive measure of their efficacy. For these experiments, this fabric was cut into 20cm2 swatches and overlooked. The reflectance of these swatches was measured to obtain a comparative measure of damage. The reflectance versus wavelength profile was measured for the "colour-damaged" fabric using the large aperture on a Texicon ICS Spectraflash 500 ™, (excluding the UV below 420nm). Sixteen measurements were taken (using 4 cloth thicknesses over the Spectraflash aperture) Six (20x20cm) overlooked swatches of the "colour-damaged" woven fabric dyed with 1% Direct Red 8 0 (unfixed) were taken, dampened with demineralised water and mixed randomly into a 2.5kg ballast load (white, desized, non-mercerised woven cotton sheeting) which had previously been put through a rinse cycle with demineralised water. Sequestrants used were: TPED: N, N, N", N" tetrakis (2-hydroxy propyl) ethylenediamine: available as Quadrol ™ L, 100% activity, ex BASF. EDDS: Ethylene diamine disuccinic acid tri sodium salt: available as Octaquest E30 ™ ex Octel 32.7%. NTA: Nitrilotriacetic acid sodium salt monohydrate 99% ex Aldrich. IDS: Iminodisuccinic acid tetra sodium salt (ex Nippon Shokubai Co. Ltd 40.2% aqueous solution) Moles of all sequestrants used in experiment = 2.14e-3 moles. A 50ml solution of 2.l4e-3 moles IDS in demineralised water was prepared. A nonwoven, embossed, polyester/rayon (50:50 mix) sheet (95gm-2) was loaded with the 50g IDS sequestrant solution described above. The IDS solution was spread out evenly over the sheet, using a glass rod. A US Whirlpool™ Super Capacity Dryer was allowed to warm up for 5 minutes on permanent press/heavy setting. The tumble dryer sheet that had been loaded with IDS was then placed inside the dryer, with the 2.5kg fabric load (ballast + 6 test swatches). The load was dried using the permanent press/heavy setting for 90 minutes. The process was repeated again with a separate, identical load. The entire regime was repeated with the other sequestrants, TPED, NTA and EDDS. The reflectance versus wavelength profile was measured for the treated fabrics using the large aperture on a Texicon ICS Spectraflash 500 ™, (excluding the UV below 420nm). Four measurements were taken for each piece of fabric in each load using 4 cloth thicknesses over the Spectraflash aperture. This gave 24 measurements per load and 4 8 readings per treatment. The reflectance value of the coloured fabric at 620nm is the most sensitive to the effects of transition metal ions in this system. The changes in reflectance at 620nm for the fabric after treatment with the various sequestrants are shown below (in table 3) for comparison. Table 3; Comparison with other sequestrants at equimolar concentration (2.14x10-3 moles). Treatment Mean reflectance at 620nm Standard Deviation 95% confidence Limits Unwashed ,46.55 0.16,. 0..16. Damaged 35.99 0.29 0.28 IDS 44.03 4.48 1.27 TPED 38.23 1.11 0.31 EDDS 39.41 2.99 0.85 NTA 38.45 1.71 0.48 From these figures it can be seen that the IDS containing system is significantly better than the other materials at the concentration used. WE CLAIM 1. Laundry drying process, which comprises tumble drying clothes in the presence of a chelating agent which has one nitrogen atom and at least four carboxylic acid groups per molecule, or a salt thereof. 2. Process according to claim 1, wherein the chelating agent is a disuccinnic acid or a salt thereof. 3. Process according to claim 2 wherein the disuccinnic acid is amine bridged. 4. Process according to any of the preceding claims wherein the chelating agent is of the general formula HOOC- (R1 - COOH) R2 - NR5 - R3 (R4- COOH) - COOH wherein R1 - R5 are each independently, C1 - C5 alkyl hydroxy-alkyl or hydrogen. 5. Process according to claim 4 wherein R1-R4 are methylene and R5 is hydrogen. 6. Process according to any of claims 1-5, conducted in the presence of one or more of a fabric softening agent, fabric conditioning agent, perfume, anti-static agent, dye-transfer inhibiting polymer, dye fixing agent, other sequestrant, chlorine scavenging agent, lubricants, cross-linking polymers, optical brightening agents. 7. A laundry drier sheet comprising a substrate and a chelating agent is of the general formula HOOC- (R1 - COOH) R2 - NR5 - R3 (R4- COOH) - COOH wherein R1-R5 are each independently, C1-C5 alkyl, hydroxy-alkyl or hydrogen Dated this 1st day of March 2004 Dr.Sanchita Ganguli Of S Majumdar & Co. Applicant"s Agent

Documents:

153-mumnp-2004-cancelled pages(27-08-2007).pdf

153-mumnp-2004-claims(granted)-(27-08-2007).doc

153-mumnp-2004-claims(granted)-(27-08-2007).pdf

153-mumnp-2004-correspondence 1(20-07-2005).pdf

153-mumnp-2004-correspondence 2(03-03-2008).pdf

153-mumnp-2004-correspondence(ipo)-(19-10-2007).pdf

153-mumnp-2004-form 13(03-10-2007).pdf

153-mumnp-2004-form 18(20-07-2005).pdf

153-mumnp-2004-form 1a(01-03-2004).pdf

153-mumnp-2004-form 2(granted)-(27-08-2007).doc

153-mumnp-2004-form 2(granted)-(27-08-2007).pdf

153-mumnp-2004-form 3(01-03-2004).pdf

153-mumnp-2004-form 5(01-03-2004).pdf

153-mumnp-2004-form-pct-ipea-409(27-08-2007).pdf

153-mumnp-2004-form-pct-isa-210(27-08-2007).pdf