Title of Invention | FABRIC CONDITIONING KIT |
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Abstract | A system, kit and package for conditioning fabrics comprises a permeable article, such as a compressible absorbent polymeric sponge or meshed article in combination with a fabric conditioning composition. The permeable article is used to disperse the fabric conditioning composition in a liquid, preferably water. |
Full Text | C4356 FORM - 2 THE PATENTS ACT, 1970 (39 of 1970) & The Patents Rules, 2006 COMPLETE SPECIFICATION (See Section 10 and Rule 13) FABRIC CONDITIONING KIT 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 performed WO 2005/063959 PCT/EP2004/013556 Fabric Conditioning Kit Field of the Invention 5 The present invention relates to a kit for rinsing fabrics, a rinse conditioning system, a method of preparing a dispersion and the use of a permeable article to prepare a dispersion. 10 Background of the Invention and. Prior Art Fabric conditioning compositions for use in the laundry are typically added to the laundry process after the washing stage. Where the laundry process involves an automatic 15 washing machine, the conditioning composition may need to be dosed either directly into the drum or via a dispensing tray. For hand-wash processes, the composition will be dosed into the hand-wash liquor. 20 Independent of the type of process, the fabric conditioning composition must firstly be sufficiently dispersed into the rinse liquor so that it can act on the fabrics being laundered. 25 If the composition is inadequately dispersed, there is a significant risk that it will not be deposited evenly on the fabric but will instead deposit at excessive concentrations on small portions thereof which in turn may lead to spotting or staining. There is also the risk that the ingredients 30 within the composition may not deposit at all and will WO 2005/063959 PCT/EP2004/013556 - 2 - instead remain in an undispersed state within the rinse liquor. This is clearly undesirable to consumers. 5 Dispersion of the composition may often not be fully complete before the composition is contacted with the fabrics to be treated. In the dispensing drawer of an automatic washing machine, this can manifest itself as a 10 build up of a gel-like residue requiring the consumer to carry out additional undesirable cleaning of the drawer. Dispersion thus remains problematic for fabric conditioning compositions. 15 Various ways of addressing this problem have been found including placing a dosed amount of the fabric conditioning composition into a container, adding water and shaking or mixing to form a pre-dispersion which can then be added to 20 the laundry cycle so as to disperse therein more easily. The drawback with this approach is that the consumer is burdoned with additional undesirable tasks and will typically be required to prepare such a pre-dispersion in advance of the laundry cycle. 25 It is thus remains desirable to provide a means for dispersing fabric conditioning compositions. Articles such as sponges are known for use with personal 30 washing products. WO 2005/063959 PCT/EP2004/013556 - 3 - A scrubbing apparatus used for personal hygiene, commonly referred to as a polymer mesh puff, is often used in cleansing the skin. These polymer mesh puffs are typically manufactured from one or more pieces of synthetic open cell 5 mesh which are bound together and manipulated into a plurality of random folds to form a generally rounded shape, or puff. US 3,226,751 discloses a combination sponge and scouring 10 device. The implement includes a soft and flexible cellular base section made of any suitable, flexible expanded plastic and scouring elements. US 3,414,928 discloses a combination sponge and scour. The 15 device includes a cellular expanded plastic base, an unexpanded material secured to a portion of the surface of the base, and a plurality of scouring elements secured to and supported by the unexpanded plastic material. 20 WO 95/00116 discloses a system for cleaning the skin which comprises a diamond mesh sponge and a liquid cleansing and moisturising composition, which system is said to have excellent lather. 25 US 3,634,901 discloses a combined cleaning and abrading or scouring utensil. US 4,980,943 discloses a cleaning glove. WO 2005/063959 PCT/EP2004/013556 4 - US 5,465,452 discloses a first extended tubular scrim having a diamond mesh pattern used to construct a personal cleaning implement. 5 US 4,154,542 is directed to a shower mitt which includes a mesh sheet of nylon net to provide a soap-retaining pocket. US 4,606,964 is directed to a bulked web composite which comprises a differentially tensioned reticulated web of 10 elastic material banded to at least one gatherable web. US 2,581,779 discloses a scouring pad said to have a greater ease of manipulation. 15 US 3,103,031 discloses a composite scouring pad made by folding plastic fibres with metallic filaments into an open batt. US 2,817,865 discloses a sponge covered strand washcloth 20 with soap pocket. The strands cross and are interwoven. US 5,144,744 discloses a hand-held ball-like polymeric mesh sponge. It is a diamond-mesh polyethylene sponge obtained from a number of netting tubes stretched over supports, 25 joined and bound together at the centre and then released from the supports. US 3,343,196 discloses a method for manufacturing a puff from an open cell mesh. 30 WO 2005/063959 PCT/EP2004/013556 - 5 - US 4,190,550 is directed to a fibrous soap filled pad which when used as a bathing aid imparts a cleansing and mildly stimulating rubbing action to human skin. 5 US 4,969,225 is directed to improved scrub brushes specifically made to contain a bar of soap for use for bathing, cleansing and the like. Commercially available "polymeric mesh sponges" are sold by 10 The Body Shop and Bynum Concepts, Inc. Other suppliers include Supremia Use in New Jersey, Sponge Factory Dominicana in the Dominican Republic and Integrated Marketing Group in Harrison, New York. 15 Typically, in the prior art, washing implements as described above find their greatest utility in combination with a liquid cleanser, since there is a need with liquid cleansers for the consumers to have an implement to grasp and with which to generate lather. 20 Often, the liquid cleanser includes a moisturising ingredient in addition to a surfactant. The desire for an implement to generate lather in a washing system including a moisturising cleansing composition is often foremost within 25 the contemplation of a consumer. Such a desire is mentioned in, for instance, WO 95/00116. By contrast, it has been long established that, for rinse conditioning products such as fabric softening compositions, 30 foaming is considered undesirable by consumers since foaming WO 2005/063959 PCT/EP2004/013556 - 6 - is associated only with a washing rather than a rinse conditioning step. Thus it is important to avoid foaming of the rinse 5 conditioning composition. Objects of the Invention The present invention seeks, to address one or more of the 10 abovementioned problems and/or to provide one or more of the abovementioned benefits. Surprisingly, it has now been found that a permeable, preferably porous article provides an excellent dispersing 15 means for fabric conditioning compositions. Statement of Invention Thus, according to the present invention there is provided a 20 system for conditioning fabrics comprising a fabric conditioning composition in combination with a permeable article for improving dispersion of the composition in a liquid. 25 The invention further provides a kit for conditioning fabric comprising a fabric conditioning composition in combination with a permeable article for improving dispersion of the composition in a liquid. 30 According to a further aspect, the invention provides a package comprising a permeable, preferably porous article, a WO 2005/063959 PCT7EP2004/013556 - 7 - fabric conditioning composition and instructions to disperse the composition in a liquid, preferably water, using the permeable article. 5 The invention also provides the use of a permeable, preferably porous article to disperse a fabric conditioning composition in a liquid, preferably water. According to yet another aspect, the invention provides a 10 method of dispersing a fabric conditioning ccrposition in a liquid, preferably water, by introducing the composition onto or into the permeable, preferably porous article, submersing the article in the liquid and agitating the article so as to assist dispersion of the co-position. 15 The invention still further provides a method of conditioning fabrics comprising dispersing a fabric conditioning composition in a liquid, preferably water, with the aid of a permeable, preferably porous article and then 20 contacting the dispersed composition with fabrics to be treated. Detailed Description of the Invention 25 In the context of the present invention, the term "comprising" denotes that the feature (s) to which it refers is/are not exhaustive and further features may be present Permeable Article 30 The system of the invention comprises a permeaoie article. WO 2005/063959 PCT/EP2004/013556 - 8 - Preferably the article is porous and/or absorbent. More preferably the article is a sponge or meshed article. 5 It is preferred that the article is compressible and it is particularly preferred that the article is resilient. Although the invention works with permeable/porous articles which have little or no compressibility and/or resilience, 10 it has been found that better dispersion can be achieved when the article is particularly compressible and/or flexible. It is believed that this is due to the article having 15 greater freedom of relative movement between different parts and/or surfaces of the article enabling a greater shearing action to occur within the article and thus better dispersion to be achieved. 20 The average diameter of the uncompressed article is typically from 2cm to 20cm, more preferably from 3cm to 15cm, most preferably from 4cm to 10cm. The article can be prepared from readily available raw 25 materials or with specially designed mesh materials. A suitable meshed article is preferably prepared from extruded tubular netting mesh which has been prepared from special strong and flexible polymeric material. Extruded 30 tubular netting mesh of this type, and particularly those WO 2005/063959 PCT/EP2004/013556 - 9 - prepared from polyethylene, have been used for the covering of meat and poultry and are readily available in industry. A polymeric meshed article preferably comprises a plurality 5 of plys of an extruded tubular netting mesh prepared from a strong flexible polymer, preferably of the group consisting of addition polymers of olefin monomers, and polyamides of polycarboxylic acids and polyamines. The plys of tubular netting mesh are typically folded upon itself numerous times 10 to form a soft ball-like polymeric mesh sponge. Alternatively, the mesh can be formed by binding a piece of tubular mesh or a sheet of mesh about a centre-point with a piece of string, and then forming a series of random folds 15 about this centre-point through various means of manipulation. In general the cross-sectional dimensions of each ply will be small in relation to the length of the ply. 20 The plys may be filaments. The ply may be elastomeric or non-elastomeric, but preferably the plys are elastomeric as this provides greater 25 freedom of movement of plys relative to each other. Preferably use of a large plurality of tiny plys offer substantial gripping surface area. Indeed, the user of the article will be enabled to thread his or her fingers through 30 the plys. While the use of plys that have a very small WO 2005/063959 PCT/EP2004/013556 - 10 - diameter as compared to ply length is envisioned primarily, the use of larger plys may also be advantageous. The article is preferably substantially spherical with a 5 plurality of floppy filaments radiating in a dense, bushy manner from a central core region. Generally, the plys will radiate outwardly in plural offset planes. The preferably open cell structure of the mesh 10 advantageously forms a structure which is highly resilient, resulting in a puff which retains its shape throughout use. In general, the diameter for the filaments will range from 0.25 to 3mm, preferably from 0.75 to 1.5mm. By "diameter" 15 in this context is meant the maximum width or thickness in the case of a ribbon-like structure or the like, or the true diameter in the case of a rod-like structure. In general, the length of the filaments is preferably from 1cm to 10cm, especially from 2 to 5cm for non-crimped filaments and from 20 2 to 15cm, especially from 5 to 12cm for crimped filaments (measured with the filament straightened). Although the preferred shape for the implement is spherical, other shapes such as a flattened oval, a football or a figure are contemplated. 25 The plys or filaments are preferably straight since this makes for a less "frilly" appearance, but they can also be curled or crimped. 30 Although the polymeric material of which the meshed article is made may be inherently mildly abrasive, it preferably WO 2005/063959 PCT/EP2004/013556 - 11 - does not incorporate abrasive particles or a scouring material. Thus, abrasives such as pumice, aluminium oxide, volcanic 5 ash, and silica are preferably omitted. Likewise, the meshed article should not be ammonia- or oxygen- releasing and preferably does not include bleaching materials. A suitable sponge is an open-cell sponge which possesses an 10 interconnected cell structure permitting limited absorption and circulation of gases and fluids. Outer surface of the material may be continuous or porous and exhibits good physical durability. Because air can pass freely between its cells, sponge offers a high degree of compressibility 15 and displays fast recovery upon release from compression. Examples of suitable sponges include both natural sponges such as sea sponges, e.g. silk, sea wool and yellow sponges and synthetic sponges, such as synthetic cellulosic sponges. 20 The system of the invention excludes "personal washing" compositions, that is compositions designed specifically for washing of the skin of human beings. 25 The system of the invention comprises the permeable article in combination with a fabric conditioning composition. WO 2005/063959 PCT/EP2004/013556 - 12 -Brief Description of the Drawings The permeable article for use in the invention will now be described by way of reference to the accompanying drawings 5 in which: Figure 1 shows a perspective view of a permeable, meshed article; 10 Figure 2 shows the meshed article of Figure 1 together with a rope; and Figure 3 shows netting material used in making the article of Fig's 1 and 2. 15 Detailed Description of the Drawings Referring to Figure 1 there is shown a representation of a polymeric hand held ball-like meshed article showing a rope 20 handle 7 used in the present invention. The ease with which a cleaning polymeric mesh sponge can be held in the hand for cleaning is shown in figure 2. A security band 13 holds the multi-layered netting mesh together to form the polymeric mesh sponge. The netting mesh that can be used in making 25 the polymeric mesh sponge is illustrated in figure 3 wherein 21 represents the mesh in stretched position. The fine polymeric filaments used in making the netting are represented by 18 with 19 representing the spot bonding of the filaments to form the open mesh 20. WO 2005/063959 PCTYEP2004/013556 - 13 - Two netting tubes at 60 cm length each can be used to make a 7cm ball sponge. They can be bundled manually with a loop or rope to form a ball-like polymeric mesh sponge. Other designs such as rectangular gloves and washings implements 5 made with the mesh material also work very well in the present invention system. Fabric Conditioning Composition 10 Cationic Fabric Softener The fabric conditioning composition will typically comprises a cationic softening material. The cationic softener is preferably a quaternary ammonium fabric softening material. 15 Particularly preferred quaternary ammonium fabric softening materials comprise two C12-28 alkyl or alkenyl groups connected to the nitrogen head group, preferably via at least one ester link. It is more preferred if the 20 quaternary ammonium material has two ester links present. Preferably, the average chain length of the alkyl or alkenyl group is at least C14, more preferably at least C16. Most preferably at least half of the chains have a length of Cis-25 It is generally preferred if the alkyl or alkenyl chains are predominantly linear, although a degree of branching, especially mid-chain branching, is within the scope of the invention. WO 2005/063959 PCT/EP2004/013556 - 14 - The first group of cationic fabric softening compounds suitable for use in the invention is represented by formula (I): 5 [(CH2)n(TR)]m I x- R1-N+-[(CH2)n(OH)]3-m (I) wherein each R is independently selected from a 05-35 alkyl 10 or alkenyl group, R represents a Ci_4 alkyl, C2-4 alkenyl or a C1-4 hydroxyalkyl group, 0 O II II 15 T is -O-C- or -C-O-, n is 0 or a number selected from 1 to 4, m is 1, 2 or 3 and denotes the number of moieties to which it relates that pend directly from the N atom, and X is an anionic group, such 20 as halides or alkyl sulphates, e.g. chloride, methyl sulphate or ethyl sulphate. Especially preferred materials within this group are di-alkenyl esters of triethanol ammonium methyl sulphate. 25 Commercial examples include Tetranyl AHT-1 (di-hardened tallow ester of triethanol ammonium methyl sulphate 85% active in 15% IPA), AT-1(di-oleic ester of triethanol ammonium methyl sulphate 90% active), L5/90 (palm ester of triethanol ammonium methyl sulphate 90% active), all ex Kao, WO 2005/063959 PCT/EP2004/013556 - 15 - and Rewoquat WE15 (C10-C20 and C16-C20 unsaturated fatty acid reaction products with triethanolamine dimethyl sulphate quaternised 90 % active), ex Witco Corporation. 5 The second group of cationic fabric softening compounds suitable for use in the invention is represented by formula (II): TR2 I 10 (R1)3N+ (CH2)n—CH X~ (II) I CH2TR2 wherein each R group is independently selected from C\-& 15 alkyl, hydroxyalkyl or C2-4 alkenyl groups; and wherein each 2 R group is independently selected from C8-28 alkyl or alkenyl groups; n is 0 or an integer from 1 to 5 and T and X are as defined above. 20 Preferred materials of this class such as 1,2 bis[tallowoyloxy]-3- trimethylammonium propane chloride and 1,2-bis[oleyloxy]-3-trimethylammonium propane chloride and their method of preparation are, for example, described in US 4137180 (Lever Brothers), the contents of which are 25 incorporated herein. WO 2005/063959 PCT/EP2004/013556 - 16 - A third group of cationic fabric softening compounds suitable for use in the invention is represented by formula (III): 1 R1 — N+ — (CH2)n — T — R2 X (III) (CH2)n — T — R2 1 10 wherein each R group is independently selected from Ci_4 2 alkyl, or C2-4 alkenyl groups; and wherein each R group is xndependently selected from Cs-28 alkyl or alkenyl groups; n ±s 0 or an integer from 1 to 5 and T and X are as defined above. 15 A fourth group of cationic fabric softening compounds suitable for use in the invention is represented by formula (IV): 20 R1 R1 — N+ — R2 X (IV) R2 WO 2005/063959 PCT/EP2004/013556 - 17 - wherein each R group is independently selected from C1-4 2 alkyl, or C2-4 alkenyl groups; and wherein each R group is independently selected from CQ-2& alkyl or alkenyl groups; and X is as defined above. 5 Iodine Value of the Parent Fatty Acyl group or Acid The iodine value of the parent fatty acyl compound or acid from which the cationic softening material is formed is 10 preferably from 0 to 140, more preferably from 0 to 100, most preferably from 0 to 60. It is especially preferred that the iodine value of the parent compound is from 0 to 20, more preferably 0 to 9, 15 most preferably 0 to 4, e.g. 2 or less or even 1.5 or less. Where the iodine value is 4 or less, the softening material provides excellent softening results and has improved resistance to oxidation and associated odour problems upon storage. 20 When unsaturated hydrocarbyl chains are present, it is preferred that the cis:trans weight ratio of the material is 50:50 or more, more preferably 60:40 or more, most preferably 70:30 or more, e.g. 85:15 or more. 25 The iodine value of the parent fatty acid or acyl compound is measured according to the method set out in WO-Al-01/46513. WO 2005/063959 PCT/EP2004/013556 - 18 - The softening material is preferably present in an amount of from 1 to 60% by weight of the total composition, more preferably from 2 to 40%, most preferably from 3 to 30% by weight. 5 Fatty Acids The composition preferably comprises a fatty acid. 10 Preferred fatty acids include hardened tallow fatty acid (available under the tradename Pristerene, ex Uniqema). The fatty acid is preferably present at a level from 0.1 to 15% by weight based on the total weight of the composition, 15 more preferably from 0.3 to 10%, most preferably from 0.5 to 5%, e.g. 0.7 to 4% by weight. Silicone 20 The composition may comprise a silicone. For instance, a suitable silicone comprises a cyclic polydi-(Ci_6)alkyl siloxane. Typical silicones of this class have the general formula 25 RaSiO(4_a)/2 wherein each R is the same or different and is selected from hydrocarbon and hydroxyl groups, {a£ being from 0 to 3. In the bulk material, {aç, typically has an average value of from 1.85-2.2. WO 2005/063959 PCT/EP2004/013556 - 19 - The silicone is preferably comprised of a homopolymer. Preferably the silicone is free of cross-linking. It is further preferred that the silicone is free of amine or amide linkages. 5 It has been found that cyclic silicones deliver excellent faster drying characteristics to fabrics and are thus preferred to linear or generally linear silicones. 10 A particularly preferred silicone comprises a cyclic poly-dimethyl-siloxane. Suitable commercially available silicones include DC245 (polydimethylcyclopentasiloxane also known as D5) , DC246 15 (polydimethylcyclohexasiloxane also known as D6), DC1184 (a pre-emulsified polydimethylpentasiloxane also known as L5) and DC347 (a pre-emulsified lOOcSt PDMS fluid), all ex Dow Corning. 20 Silicone form The silicone may be received and incorporated into the composition either directly as an oil or pre-emulsified. 25 Pre-emulsification is typically required when the silicone is of a more viscous nature. Suitable emulsifiers include cationic emulsifiers, nonionic emulsifiers or mixtures thereof. WO 2005/063959 PCT/EP2004/013556 - 20 - Silicone viscosity The reference to the viscosity of the silicone denotes either the viscosity before emulsification when the silicone 5 is provided as an emulsion for incorporation into the fabric conditioning composition or the viscosity of the silicone itself when provided as an oil for incorporation into the fabric conditioning composition. 10 The silicone preferably has a viscosity (as measured on a Brookfield RV4 viscometer at 25°C using spindle No.4 at 100 rpm) of from lcSt to less than 10,000 cSt (centi-Stokes), preferably from lcSt to 5,000cSt, more preferably from 2cSt to l,000cSt and most preferably 2cSt to lOOcSt. 15 It has been found that drying time can be reduced using silicones having a viscosity of from 1 to 500,000 cSt. However, significantly improved results are obtained when the viscosity is from 1 to less than 10,000cSt. 20 The silicone is preferably present at a level of from 0.5 to 20%, more preferably from 1 to 12%, most preferably from 1 to 8% by weight of active ingredient, based on the total weight of the composition. 25 Fatty Alcohol — co-active softener Optionally and advantageously, one or more un-alkoxylated fatty alcohols are present in the composition. 30 WO 2005/063959 PCT/EP2004/013556 - 22 - Preferred fatty esters include fatty monoesters, such as glycerol monostearate (hereinafter referred to as "GMS"). If GMS ±s present, then it is preferred that the level of GMS in the composition is from 0.01 to 10% by weight, based 5 on the -total weight of the composition. The co-active softener may also comprise an oily sugar derivative. Suitable oily sugar derivatives, their methods of manufacture and their preferred amounts are described in 10 WO-Al-01/46361 on page 5 line 16 to page 11 line 20, the disclosure of which is incorporated herein. Nonionic surfactant 15 It is preferred that the compositions further comprise a nonionic surfactant. Typically these can be included for the purpose of stabilising the compositions. Suitable nonionic surfactants include addition products of 20 ethylene oxide and/or propylene oxide with fatty alcohols, fatty acids and fatty amines. Any of the alkoxylated materials of the particular type described hereinafter can be used as the nonionic 25 surfactant. Suitable surfactants are substantially water soluble surfactants of the general formula: WO 2005/063959 PCT/EP2004/013556 - 23 - R—Y—(C2H40)Z C2H4OH where R is selected from the group consisting of primary, 5 secondary and branched chain alkyl and/or acyl hydrocarbyl groups; primary, secondary and branched chain alkenyl hydrocarbyl groups; and primary, secondary and branched chain alkenyl-substituted phenolic hydrocarbyl groups; the hydrocarbyl groups having a chain length of from 8 to about 10 25, preferably 10 to 20, e.g. 14 to 18 carbon atoms. In the general formula for the alkoxylated nonionic surfactant, Y is typically: 15 --0— , —C(0)0— , — C(0)N(R)— or -C(0)N(R)R-- in which R has the meaning given above or can be hydrogen; and Z is preferably from 8 to 40, more preferably from 10 to 30, most preferably from 11 to 25, e.g. 12 to 22. 20 The level of alkoxylation, Z, denotes the average number of alkoxy groups per molecule. Preferably the nonionic surfactant has an HLB of from about 25 7 to about 20, more preferably from 10 to 18, e.g. 12 to 16. Examples of nonionic surfactants follow. In the examples, the integer defines the number of ethoxy (EO) groups in the molecule. WO 2005/063959 PCT/EP2004/013556 - 24 - A. Straight-Chain, Primary Alcohol Alkoxylates The deca —, undeca-, dodeca-, tetradeca-, and pentadecaethoxylates of n-hexadecanol, and n-octadecanol 5 having an HLB within the range recited herein are useful viscosity/dispersibility modifiers in the context of this invention. Exemplary ethoxylated primary alcohols useful herein as the viscosity/dispersibility modifiers of the compositions are C18 EO(10); and C18 EO(ll). The ethoxylates 10 of mixed natural or synthetic alcohols in the "tallow" chain length range are also useful herein. Specific examples of such materials include tallow alcohol-EO(ll) , tallow alcohol-EO(18) , and tallow alcohol-EO (25), coco alcohol-EO(10), coco alcohol-EO(15), coco alcohol-EO(20) and coco 15 alcohol-EO(25) . B. Straight-Chain, Secondary Alcohol Alkoxylates The deca—, undeca-, dodeca-, tetradeca-, pentadeca-, 20 octadeca —, and nonadeca-ethoxylates of 3-hexadecanol, 2-octadecanol, 4-eicosanol, and 5-eicosanol having an HLB within the range recited herein are useful viscosity and/or dispersibility modifiers in the context of this invention. Exemplary ethoxylated secondary alcohols useful herein as 25 the viscosity and/or dispersibility modifiers of the compositions are: Ci6 EO(ll); C20 EO(ll); and Ci6 EO(14). WO 2005/063959 PCT/EP2004/013556 - 25 - C. Alkyl Phenol Alkoxylates As in the case of the alcohol alkoxylates, the hexa- to octadeca-ethoxylates of alkylated phenols, particularly 5 monohydric alkylphenols, having an HLB within the range recited herein are useful as the viscosity and or dispersibility modifiers of the instant compositions. The hexa- to octadeca-ethoxylates of p-tri-decylphenol, m-pentadecylphenol, and the like, are useful herein. 10 Exemplary ethoxylated alkylphenols useful as the viscosity and/or dispersibility modifiers of the mixtures herein are: p-tridecylphenol EO(ll) and p-pentadecylphenol EO(18). As used herein and as generally recognized in the art, a 15 phenylene group in the nonionic formula is the equivalent of an alkylene group containing from 2 to 4 carbon atoms. For present purposes, nonionics containing a phenylene group are considered to contain an equivalent number of carbon atoms calculated as the sum of the carbon atoms in the alkyl group 20 plus about 3.3 carbon atoms for each phenylene group. D. Olefinic Alkoxylates The. alkenyl alcohols, both primary and secondary, and 25 alkenyl phenols corresponding to those disclosed immediately hereinabove can be ethoxylated to an HLB within the range recited herein and used as the viscosity and/or dispersibility modifiers of the instant compositions. WO 2005/063959 PCT/EP2004/013556 - 26 - E. Branched Chain Alkoxylates Branched chain primary and secondary alcohols which are available from the well-known "OXO" process can be 5 ethoxylated and employed as the viscosity and/or dispersibility modifiers of compositions herein. F. Polyol Based Surfactants 10 Suitable polyol based surfactants include sucrose esters such as sucrose monooleates, alkyl polyglucosides such as stearyl monoglucosides and stearyl triglucoside and alkyl polyglycerols.. 15 The above nonionic surfactants are useful in the present compositions alone or in combination, and the term "nonionic surfactant" encompasses mixed nonionic surface active agents. 20 The nonionic surfactant is preferably present in an amount of from- 0.01 to 10%, more preferably 0.1 to 5%, most preferably 0.35 to 3.5%, e.g. 0.5 to 2% by weight, based on the total weight of the composition. 25 Perfume The compositions of the invention preferably comprise one or more perfumes in order to provide an odour desirable to consumers. 30 WO 2005/063959 PCT/EP2004/013556 - 27 - It is well known that perfume is typically provided as a mixture of components. Suitable components for use in the perfume include those described in '"Perfume and Flavor Chemicals (Aroma Chemicals) by Steffen Arctander, published 5 by the author, 1969, Montclait, N.J. (US), reprinted 1st April 1982 Library of Congress Catalog Number 75-91398, incorporated herein. Furthermore, it is preferred that the perfume comprises 10 substantive perfume ingredients as described in US-A1-2003/0050220 paragraphs 60 to 72, incorporated herein. The perfume is preferably present in an amount from 0.01 to 10% by weight, more preferably 0.05 to 5% by weight, most 15 preferably 0.5 to 4.0% by weight, based on the total weight of the composition. Liquid Carrier 20 A liquid carrier is preferably employed in the instant compositions. The liquid carrier is at least partly water due to its low cost, relative availability, safety, and environmental compatibility. The level of water in the liquid carrier is more than about 50%, preferably more than 25 about 80%, more preferably more than about 85%, by weight of the carrier. The level of liquid carrier is greater than about 50%, preferably greater than about 65%, more preferably greater than about 70%. Mixtures of water and a low molecular weight, e.g. 30 lower alcohol such as ethanol, propanol, isopropanol or butanol are useful as the carrier liquid. Low molecular WO 2005/063959 PCT/EP2004/013556 - 28 - weight alcohols including monohydric, dihydric (glycol, etc.) trihydric (glycerol, etc.), and polyhydric (polyols) alcohols are also suitable carriers for use in the compositions of the present invention. 5 Polymeric viscosity control agents It is useful, though not essential, if the compositions comprise one or more polymeric viscosity control agents. 10 Suitable polymeric viscosity control agents include nonionic and cationic polymers, such as hydrophobically modified cellulose ethers (e.g. Natrosol Plus, ex Hercules), cationically modified starches (e.g. Softgel BDA and Softgel BD, both ex Avebe). A particularly preferred viscosity 15 control agent is a copolymer of methacrylate and cationic acrylamide available under the tradename Flosoft 200 (ex SNF Floerger) .' Nonionic and/or cationic polymers are preferably present in 20 an amount of 0.01 to 5wt%, more preferably 0.02 to 4wt%, based on the total weight of the composition. Antifoaming Agent 25 It is particularly preferred that the composition comprises an antifoaming agent. The antifoaming agent is preferably present at a level of from 0.001 to 5% by weight, more preferably 0.002 to 3% by 30 weight, most preferably 0.003 to 1% by weight, e.g. 0.004 to WO 2005/063959 PCT/EP2004/013556 - 29 - 0.7% by weight, based on the total weight of the composition. A typical antifoaming agent suitable for use in the 5 composition is DOW CORNING® 1520 Silicone antifoam (a 20% active silicone emulsion). Further Optional Ingredients 10 Other optional nonionic softeners, bactericides, soil-releases agents may also be incorporated in the compositions of the invention. The compositions may also contain one or more optional 15 ingredients conventionally included in fabric conditioning compositions such as pH buffering agents, perfume carriers, fluorescers, colourants, hydrotropes, antiredeposition agents, polyelectrolytes, enzymes, optical brightening agents, pearlescers, anti-shrinking agents, anti-wrinkle 20 agents, anti-spotting agents, antioxidants, sunscreens, anti-corrosion agents, drape imparting agents, dye fixatives, sequestrants, preservatives, anti-static agents, ironing aids and dyes. 25 Product Form The fabric conditioning composition may be a liquid, such as an aqueous liquid, preferably an aqueous dispersion of the cationic softening material, a soft solid such as a gel, 30 cream or paste, or a solid such as a granular material. Preferably the product is a liquid or soft solid. WO 2005/063959 PCT/EP2004/013556 - 30 - The invention is especially useful for very high viscosity compositions since these are often much harder to disperse than low viscosity compositions. In particular, it is 5 preferred that the composition has a viscosity as measured using a Haake Rotoviscometer with MV1 cup and Bob at 106s-l of greater than 200mPaS, more preferably greater than 400mPaS, most preferably greater than 500mPaS, e.g. greater than 600mPaS. Conventional liquid fabric conditioning 10 compositions have a viscosity of from 20-150mPaS. Product Use The composition is preferably used in a domestic laundry 15 operation such as an automatic washing machine, e.g. a top-loading washing machine, or a hand-washing laundry operation. It is particularly preferred that the present invention is used in a hand-washing operation where the fabrics are laundered by hand in a receptacle such as, for 20 example, a bucket, sink, bath or other suitably sized container. The system of the invention may, for instance, be sold in the form of a pack or kit. 25 The meshed article can thus be packaged together with a separate fabric conditioning composition such that none of the composition is impregnated or otherwise initially incorporated onto or into the implement. Of course, it is 30 envisaged that the fabric conditioning composition can be, in use, dosed either onto and/or into the meshed article and then placed in the wash/rinse liquor and dispersed or dosed WO 2005/063959 PCT/EP2004/013556 - 31 - directly into the wash/rinse liquor and then the meshed article is introduced into the liquor and used to disperse the composition or a combination of the above. 5 It is also envisaged that the kit may be supplied to the consumer with the permeable article pre-dosed with a fabric conditioning composition. Thus, at least initially, the consumer is not required to dose the permeable article with the fabric conditioning composition. 10 Examples The invention will now be illustrated by the following non-limiting examples. Further modifications will be apparent 15 to the person skilled in the art. Samples of the invention are represented by a number. Comparative samples are represented by a letter. 20 All values are % by weight of the active ingredient unless stated otherwise. The following fabric conditioning composition was prepared by melting together the quat, fatty acid, and lecithin, 25 adding this mixture to heated water, milling the mixture and then allowing it to cool. During cooling the citric acid, calcium chloride, perfume and minors were added. WO 2005/063959 PCT/EP2004/013556 - 32 - Table 1 Ingredient Wt% Quat(l) 14.10 Fatty acid (2) 1.20 Lecithin (3) 2.00 Calcium chloride (4) 0.06 Citric acid 0.025 Perfume 1.02 Water + minors To 100 5 (1) ARQUAD 2HT-75E (ex Akzo) (2) PRISTERINE 4916 (ex Uniqema) (3) ALCOLEC Z7 (ex American Lecithin Company) (4) Dosed at a concentration of 10% 10 The viscosity of the resulting product was greater than 8000 mPas measured at 106s-l using a Rotoviscometer and MV1 cup and bob. A comparative product (sample A) was prepared by placing 15 3.5g/51 of the composition onto hands, submersing hands in 51 water and then rubbing together for 30 seconds. A dispersion according to the invention (sample B) was made using a meshed article by dispersing 3.5g/51 of the 20 composition onto and into the meshed article and then submersing the meshed article into 51 water and agitating the meshed article for 30 seconds. WO 2005/063959 PCT/EP2004/013556 - 33 - The dispersion was then visually assessed by a test panel of 4 people on a scale of 0 to 5 wherein 0 represents full dispersion and 5 represents extremely poor dispersion. 5 The results are given in the following table: Table 2 Panellist Sample A Sample B 1 3.5 0.5 2 5 1 3 4.5 0.5 4 4.5 0.5 C4356(C) COM 34 CLAIMS 1. A method of dispersing a fabric conditioning composition having a viscosity, measured using a Haake Rotorisiometer with MV1 cup and Bob at 106s*1, of greater than 5 200mPaS, in a rinse liquid in a top-loading washing machine or in a container used in a hand-washing laundry operation, the method comprising introducing said fabric conditioning composition onto or into a permeable article, submersing the article in the liquid and agitating the article so as to assist dispersion of the composition. 10 2. A method of dispersing a fabric conditioning composition in which the viscosity of the fabric conditioning composition measured using a Haake Rotorisiometer with MV1 cup and Bob at 106s"1, is greater than 400mPaS. 3. A method of dispersing a fabric conditioning composition as claimed in Claim 2 in 15 which the viscosity of the fabric conditioning composition measured using a Haake Rotorisiometer with MV1 cup and Bob at 106s"1, is greater than 500mPaS. 4. A method of dispersing a fabric conditioning composition as claimed in Claim 3 in which the viscosity of the fabric conditioning composition measured using a Haake 20 Rotorisiometer with MV1 cup and Bob at 106s"1, is greater than 600mPaS. 5. A method of dispersing a fabric conditioning composition as claimed in any preceding claim in which the permeable article is an open-cell sponge or meshed article. 25 6. A method of dispersing a fabric conditioning composition as claimed in Claim 5 in which the meshed article is prepared from extruded tubular netting mesh. Dated this 23rd day of June 2006 HINDUSTAN LEVER LTD (S Venkatramani) Sr Patents Manager |
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742-mumnp-2006-cancelled pages(24-03-2008).pdf
742-mumnp-2006-claims (granted)(24-03-2008).pdf
742-mumnp-2006-correspondance-received.pdf
742-MUMNP-2006-CORRESPONDENCE(25-08-2008).pdf
742-MUMNP-2006-CORRESPONDENCE(29-9-2008).pdf
742-MUMNP-2006-CORRESPONDENCE(8-2-2012).pdf
742-mumnp-2006-correspondence(ipo)-(21-11-2008).pdf
742-mumnp-2006-correspondence1(27-10-2006).pdf
742-mumnp-2006-correspondence2(24-03-2008).pdf
742-mumnp-2006-description (complete).pdf
742-mumnp-2006-drawing(24-03-2008).pdf
742-mumnp-2006-form 1(23-06-2006).pdf
742-mumnp-2006-form 13(24-09-2007).pdf
742-mumnp-2006-form 18(27-08-2006).pdf
742-mumnp-2006-form 2(granted)-(24-03-2008).pdf
742-mumnp-2006-form 3(23-06-2006).pdf
742-mumnp-2006-form 5(23-06-2006).pdf
742-mumnp-2006-form-pct-ipea-409.pdf
742-mumnp-2006-form-pct-ipea-416.pdf
742-mumnp-2006-form-pct-isa-210(23-06-2006).pdf
742-mumnp-2006-other documents(24-09-2007).pdf
742-mumnp-2006-pct-search report.pdf
742-mumnp-2006-power of attorney(24-03-2008).pdf
Patent Number | 227345 | ||||||||
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Indian Patent Application Number | 742/MUMNP/2006 | ||||||||
PG Journal Number | 10/2009 | ||||||||
Publication Date | 06-Mar-2009 | ||||||||
Grant Date | 07-Jan-2009 | ||||||||
Date of Filing | 23-Jun-2006 | ||||||||
Name of Patentee | HINDUSTAN UNILEVER LIMITED | ||||||||
Applicant Address | Hindustan Lever House,165-166 Backbay Reclamation,Mumbai 400 020. | ||||||||
Inventors:
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PCT International Classification Number | C11D 17/04 | ||||||||
PCT International Application Number | PCT/EP2004/013556 | ||||||||
PCT International Filing date | 2004-11-29 | ||||||||
PCT Conventions:
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