Classifications

• • C—CHEMISTRY; METALLURGY
  • C11—ANIMAL OR VEGETABLE OILS, FATS, FATTY SUBSTANCES OR WAXES; FATTY ACIDS THEREFROM; DETERGENTS; CANDLES
  • C11D—DETERGENT COMPOSITIONS; USE OF SINGLE SUBSTANCES AS DETERGENTS; SOAP OR SOAP-MAKING; RESIN SOAPS; RECOVERY OF GLYCEROL
  • C11D3/00—Other compounding ingredients of detergent compositions covered in group C11D1/00
  • C11D3/16—Organic compounds
  • C11D3/20—Organic compounds containing oxygen
  • C11D3/22—Carbohydrates or derivatives thereof
  • C11D3/222—Natural or synthetic polysaccharides, e.g. cellulose, starch, gum, alginic acid or cyclodextrin
  • C11D3/227—Natural or synthetic polysaccharides, e.g. cellulose, starch, gum, alginic acid or cyclodextrin with nitrogen-containing groups
• • C—CHEMISTRY; METALLURGY
  • C11—ANIMAL OR VEGETABLE OILS, FATS, FATTY SUBSTANCES OR WAXES; FATTY ACIDS THEREFROM; DETERGENTS; CANDLES
  • C11D—DETERGENT COMPOSITIONS; USE OF SINGLE SUBSTANCES AS DETERGENTS; SOAP OR SOAP-MAKING; RESIN SOAPS; RECOVERY OF GLYCEROL
  • C11D1/00—Detergent compositions based essentially on surface-active compounds; Use of these compounds as a detergent
  • C11D1/38—Cationic compounds
  • C11D1/65—Mixtures of anionic with cationic compounds
• • C—CHEMISTRY; METALLURGY
  • C11—ANIMAL OR VEGETABLE OILS, FATS, FATTY SUBSTANCES OR WAXES; FATTY ACIDS THEREFROM; DETERGENTS; CANDLES
  • C11D—DETERGENT COMPOSITIONS; USE OF SINGLE SUBSTANCES AS DETERGENTS; SOAP OR SOAP-MAKING; RESIN SOAPS; RECOVERY OF GLYCEROL
  • C11D17/00—Detergent materials or soaps characterised by their shape or physical properties
  • C11D17/04—Detergent materials or soaps characterised by their shape or physical properties combined with or containing other objects
  • C11D17/041—Compositions releasably affixed on a substrate or incorporated into a dispensing means
  • C11D17/042—Water soluble or water disintegrable containers or substrates containing cleaning compositions or additives for cleaning compositions
  • C11D17/043—Liquid or thixotropic (gel) compositions
• • C—CHEMISTRY; METALLURGY
  • C11—ANIMAL OR VEGETABLE OILS, FATS, FATTY SUBSTANCES OR WAXES; FATTY ACIDS THEREFROM; DETERGENTS; CANDLES
  • C11D—DETERGENT COMPOSITIONS; USE OF SINGLE SUBSTANCES AS DETERGENTS; SOAP OR SOAP-MAKING; RESIN SOAPS; RECOVERY OF GLYCEROL
  • C11D3/00—Other compounding ingredients of detergent compositions covered in group C11D1/00
  • C11D3/0005—Other compounding ingredients characterised by their effect
  • C11D3/001—Softening compositions
  • C11D3/0015—Softening compositions liquid
• • C—CHEMISTRY; METALLURGY
  • C11—ANIMAL OR VEGETABLE OILS, FATS, FATTY SUBSTANCES OR WAXES; FATTY ACIDS THEREFROM; DETERGENTS; CANDLES
  • C11D—DETERGENT COMPOSITIONS; USE OF SINGLE SUBSTANCES AS DETERGENTS; SOAP OR SOAP-MAKING; RESIN SOAPS; RECOVERY OF GLYCEROL
  • C11D1/00—Detergent compositions based essentially on surface-active compounds; Use of these compounds as a detergent
  • C11D1/38—Cationic compounds
  • C11D1/62—Quaternary ammonium compounds

Definitions

• This invention relates to unit dose products which deliver liquid fabric treatment compositions.
• this invention relates to single compartment, pouched, non-aqueous compositions providing fabric cleaning and fabric softening benefits delivered through an easy to handle unit dose system.
• Fabric cleaning/softening products come in a number of forms, such as granules, liquids, tablets, and pouches. Each form has its own advantages and disadvantages.
• the pouches comprise a non-aqueous liquid composition surrounded by a water-soluble film, such as a polyvinyl alcohol film.
• a water-soluble film such as a polyvinyl alcohol film.
• EP 339 707 discloses a non-aqueous detergent composition contained in a PVA film.
• WO 01/81 520 discloses a wash-cycle single compartment unit dose softener composition.
• WO 01/85 888 discloses a unit-dose composition delivering fabric softening benefits and comprising up to 5% wt. or less of surfactants.
• the disadvantage of this system is the low cleaning performance due to the low surfactant content.
• the present invention provides a solution of this problem by utilizing cationic fabric softening agents with a low cationic charge density or by utilizing compositions with a high molar ratio of anionic surfactants to cationic softener, or a combination thereof.
• prior art unit dose products have shortcomings with respect to dissolving quickly and completely upon contact with water.
• the pouched compositions of the present invention demonstrate very good cleaning performance and very good fabric softening, especially fabric softening performance. Additionally, it has been found that the pouched compositions of the present invention demonstrate better solubility and/or lower residues formation.
• the present invention relates to unit dose products in the form of liquid fabric treatment compositions contained in single compartment water-soluble pouches.
• the inner space of each pouch comprises
• the water-soluble pouches are typically in direct contact with the compositions.
• a method of producing unit dose products according to the present invention and the use of unit dose products according to the present invention to treat fabrics and to thereby impart fabric-cleaning and fabric-softening benefits via single compartment water-soluble pouches are also subjects of the present invention.
• the method of producing the unit dose products herein involves separate preparation of the fabric cleaning system and of the fabric softening system, and thereinafter combining the two systems.
• the pouch herein is typically a closed structure, made of materials described herein, enclosing a volume space.
• the pouch contains a fabric treatment composition, which can be in any suitable form, provided the composition is at least partly liquid.
• the composition must comprise a fabric cleaning system and a fabric softening system.
• the pouch and volume space thereof can be of any form, shape and material which is suitable to hold the composition, e.g. without allowing the release of the composition from the pouch prior to contact of the pouch with water during laundering.
• the exact execution will depend on, for example, the type and amount of the composition in the pouch, the characteristics required from the pouch to hold, protect and deliver or release the compositions, provided that the pouch is a single compartment water-soluble pouch.
• the pouch has a spheroid shape.
• the pouch may be of such a size that it conveniently contains either a unit dose amount of the composition herein, suitable for the required operation, for example one wash, or only a partial dose, to allow the consumer greater flexibility to vary the amount used, for example depending on the size and/ or degree of soiling of the wash load.
• the pouch is typically made from a water-soluble film.
• Preferred water-soluble films are polymeric materials, preferably polymers which are formed into a film.
• the material in the form of a film can for example be obtained by casting, blow-moulding, extrusion or blow extrusion of the polymer material, as known in the art.
• the water-soluble films for use herein typically have a solubility of at least 50%, preferably at least 75% or even at least 95%, as measured by the method set out hereinafter using a glass-filter with a maximum pore size of 50 microns, namely:
• the water-soluble film and preferably the pouch as a whole is stretched during formation and/or closing of the pouch, such that the resulting pouch is at least partially stretched. This is to reduce the amount of film required to enclose the volume space of the pouch.
• the degree of stretching indicates the amount of stretching of the film by the reduction in the thickness of the film. For example, if by stretching the film, the thickness of the film is exactly halved then the stretch degree of the stretched film is 100%. Also, if the film is stretched so that the film thickness of the stretched film is exactly a quarter of the thickness of the unstretched film then the stretch degree is exactly 200%.
• the thickness and hence the degree of stretching is non-uniform over the pouch, due to the formation and closing process.
• Another advantage of stretching the pouch is that the stretching action, when forming the shape of the pouch and/or when closing the pouch, stretches the pouch non-uniformly, which results in a pouch which has a non-uniform thickness. This allows control of the dissolution of water-soluble pouches herein.
• the pouch is stretched such that the thickness variation in the pouch formed of the stretched water-soluble film is from 10 to 1000%, preferably 20% to 600%, or even 40% to 500% or even 60% to 400%. This can be measured by any method, for example by use of an appropriate micrometer.
• the pouch is made from a water-soluble film that is stretched, and wherein the film has a stretch degree of from 40% to 500%, preferably from 40% to 200%.
• the film preferably has a thickness of from 1 ⁇ m to 200 ⁇ m, more preferably from 15 ⁇ m to 150 ⁇ m, even more preferably from 30 ⁇ m to 100 ⁇ m.
• the fabric treatment composition is a composition to be delivered to water and thus, the pouch and the compartment thereof are designed such that its contents are released at, or very shortly after, the time of placing the pouch in water.
• the pouch with is compartment is formed from a material which is water-soluble.
• the component is delivered to the water within 3 minute, preferably even within 2 minutes or even within 1 minute after contacting the pouched composition with water.
• the pouch can be made from any material suitable for use in conventional unit dose laundry products.
• polymer and/or copolymers and/or derivatives thereof are preferred.
• Preferred polymer and/or copolymers and/or derivatives thereof are selected from polyvinyl alcohol (PVA), polyvinyl pyrrolidone, polyalkylene oxides, acrylamide, acrylic acid, cellulose, cellulose ethers, cellulose esters, cellulose amides, polyvinyl acetates, polycarboxylic acids and salts, polyaminoacids or peptides, polyamides, polyacrylamide, copolymers of maleic/acrylic acids, polysaccharides including starch and gelatine, natural gums such as xanthum and carragum; and mixtures thereof.
• PVA polyvinyl alcohol
• polyvinyl pyrrolidone polyalkylene oxides
• acrylamide acrylic acid
• cellulose cellulose ethers
• cellulose esters cellulose amides
• the polymer is selected from polyacrylates and water-soluble acrylate copolymers, methylcellulose, carboxymethylcellulose sodium, dextrin, ethylcellulose, hydroxyethyl cellulose, hydroxypropyl methylcellulose, maltodextrin, polymethacrylates, and mixtures thereof, most preferably polyvinyl alcohols, polyvinyl alcohol copolymers, hydroxypropyl methyl cellulose (HPMC), and mixtures thereof.
• the level of polymer in the film for example a PVA polymer, is at least 60%.
• the polymer can have any weight average molecular weight, preferably from 1000 to 1,000,000, or even from 10,000 to 300,000 or even from 15,000 to 200,000 or even from 20,000 to 150,000.
• Mixtures of polymers can also be used. This may in particular be beneficial to control the mechanical and/or dissolution properties of the compartment or pouch, depending on the application thereof and the required needs. For example, it may be preferred that a mixture of polymers is present in the material of the pouch compartment, whereby one polymer material has a higher water-solubility than another polymer material, and/or one polymer material has a higher mechanical strength than another polymer material.
• a mixture of polymers is used, having different weight average molecular weights, for example a mixture of PVA or a copolymer thereof of a weight average molecular weight of 10,000 to 40,000, preferably around 20,000, and of PVA or copolymer thereof, with a weight average molecular weight of 100,000 to 300,000, preferably around 150,000.
• polymer blend compositions for example comprising hydrolytically degradable and water-soluble polymer blend such as polylactide and polyvinyl alcohol, achieved by the mixing of polylactide and polyvinyl alcohol, typically comprising 1% to 60% by weight polylactide and approximately from 40% to 99% by weight polyvinyl alcohol.
• the polymer present in the film is from 60% to 98% hydrolysed, preferably from 80% to 90%, to improve the dissolution of the film.
• Most preferred films are films which comprise a PVA polymer with similar properties to the film which comprises a PVA polymer and is known under the trade reference M8630, as sold by Monosol LLC of Gary, Indiana, US. Another preferred film is known under the trade reference PT-75, sold by Aicello Chemical Europe GmbH, Carl-Zeiss-Strasse 43, 47445 Moers, DE.
• the film herein may comprise other additive ingredients besides the polymer or polymer material.
• plasticisers for example glycerol, ethylene glycol, diethyleneglycol, propylene glycol, sorbitol and mixtures thereof, additional water, disintegrating aids.
• the composition herein is a detergent composition, that the film itself comprises a detergent additive to be delivered to the wash water, for example, organic polymeric soil release agents, dispersants, dye transfer inhibitors.
• the pouch herein comprises a fabric treatment composition, and typically the composition is contained in the volume space of the pouch.
• the pouch contains a liquid fabric treatment composition.
• liquid it is meant that the composition needs to have a fluid viscosity as to be pourable.
• the fabric treatment composition can be in the form of a conventional liquid, or a gel.
• the fabric treatment composition must contain a fabric cleaning system, comprising more than 5% by weight of the fabric treatment composition of at least one anionic surfactant, and a fabric softening system comprising at least one fabric softening active selected from the group consisting of (i) cationic ammonium-based fabric softening compounds comprising at least one carbonyl functionality; wherein the molar ratio of anionic surfactant to ammonium-based fabric softener is at least 3:1; (ii) cationic guar gums with a charge density between 0.2 meq/gm to 5.0 meq/gm; and (iii) mixtures thereof.
• One essential element of the compositions used in the present invention is a fabric cleaning system.
• the surfactant is present at levels above 5%, preferably between 10% to 80% and more preferably from 20% to 60% by weight of the fabric treatment composition.
• Such a fabric cleaning system comprises at least one anionic surfactant.
• the cleaning system further comprises a detersive surfactant selected from the group consisting of nonionic, cationic, zwitterionic, and amphoteric surfactants, and mixtures thereof and described in detail hereinafter.
• at least 75% wt. of total surfactant in the cleaning system comprises non-alkoxylated anionic surfactants and less than 25% wt.
• a cleaning system surfactant system with at least 75% wt. of all surfactants being a non-alkoylated surfactant and less than 25% wt. of all surfactants being an alkoxylated surfactant is used in combination with a fabric softening system comprising a cationic ammonium-based fabric softening compound with at least one carbonyl functionality.
• any anionic surfactant is suitable for the purpose of the present invention.
• certain anionic surfactants as described hereinafter are more preferred.
• At least an anionic surfactant is present, preferably at least an sulfonic acid surfactant, such as a linear alkyl benzene sulfonic acid, but salt forms may also be used.
• at least an anionic surfactant and an nonionic surfactant are present in the fabric cleaning system.
• the anionic surfactant(s), are preferably present at levels of at least 7.5% by weight of the fabric treatment composition. More preferably anionic surfactant is present at levels of from 10% or even at least 15%, or even from 22.5% by weight of the fabric treatment composition.
• Anionic sulfonate or sulfonic acid surfactants suitable for use herein include the acid and salt forms of a C5-C20, more preferably a C10-C16, more preferably a C11-C13 alkylbenzene sulfonates, alkyl ester sulfonates, C6-C22 primary or secondary alkane sulfonates, sulfonated polycarboxylic acids, and any mixtures thereof, but preferably C11-C13 alkylbenzene sulfonates.
• Anionic sulfate salts or acids surfactants suitable for use in the cleaning system of the compositions of the invention include the primary and secondary alkyl sulfates, having a linear or branched C9-C22 alkyl or alkenyl moiety or more preferably C12-C18 alkyl.
• beta-branched alkyl sulfate surfactants or mixtures of commercial available materials having a weight average (of the surfactant or the mixture) branching degree of at least 50% or even at least 60% or even at least 80% or even at least 95%. It has been found that these branched sulfate surfactants provide a much better viscosity profile, when clays are present, particular when 5% or more clay is present.
• the only sulfate surfactant is such a highly branched alkyl sulfate surfactant, namely referred may be that only one type of commercially available branched alkyl sulfate surfactant is present, whereby the weight average branching degree is at least 50%, preferably at least 60% or even at least 80%, or even at least 90%.
• Preferred is for example Isalchem, as available form Condea.
• Mid-chain branched alkyl sulfates or sulfonates are also suitable anionic surfactants for use in the cleaning systems of the present invention.
• Preferred are the mid-chain branched alkyl sulfates.
• Preferred mid-chain branched primary alkyl sulfate surfactants are of the formula
• These surfactants have a linear primary alkyl sulfate chain backbone (i.e., the longest linear carbon chain which includes the sulfated carbon atom), which preferably comprises from 12 to 19 carbon atoms and their branched primary alkyl moieties comprise preferably a total of at least 14 and preferably no more than 20, carbon atoms.
• the average total number of carbon atoms for the branched primary alkyl moieties is preferably within the range of from greater than 14.5 to 17.5.
• the cleaning system preferably comprises at least one branched primary alkyl sulfate surfactant compound having a longest linear carbon chain of not less than 12 carbon atoms or not more than 19 carbon atoms, and the total number of carbon atoms including branching must be at least 14, and further the average total number of carbon atoms for the branched primary alkyl moiety is within the range of greater than 14.5 to 17.5.
• Preferred mono-methyl branched primary alkyl sulfates are selected from the group consisting of: 3-methyl pentadecanol sulfate, 4-methyl pentadecanol sulfate, 5-methyl pentadecanol sulfate, 6-methyl pentadecanol sulfate, 7-methyl pentadecanol sulfate, 8-methyl pentadecanol sulfate, 9-methyl pentadecanol sulfate, 10-methyl pentadecanol sulfate, 11-methyl pentadecanol sulfate, 12-methyl pentadecanol sulfate, 13-methyl pentadecanol sulfate, 3-methyl hexadecanol sulfate, 4-methyl hexadecanol sulfate, 5-methyl hexadecanol sulfate, 6-methyl hexadecanol
• Preferred di-methyl branched primary alkyl sulfates are selected from the group consisting of: 2,3-methyl tetradecanol sulfate, 2,4-methyl tetradecanol sulfate, 2,5-methyl tetradecanol sulfate, 2,6-methyl tetradecanol sulfate, 2,7-methyl tetradecanol sulfate, 2,8-methyl tetradecanol sulfate, 2,9-methyl tetradecanol sulfate, 2,10-methyl tetradecanol sulfate, 2,11-methyl tetradecanol sulfate, 2,12-methyl tetradecanol sulfate, 2,3-methyl pentadecanol sulfate, 2,4-methyl pentadecanol sulfate, 2,5-methyl pentadecanol sulfate, 2,6-methyl penta
• anionic surfactants herein are present in the form of sodium salts.
• any nonionic surfactant is suitable for use in the cleaning system of the present invention.
• certain nonionic surfactants as described herein after are more preferred.
• alkoxylated nonionic surfactants can be comprised by the composition herein.
• Ethoxylated and propoxylated nonionic surfactants are preferred.
• Preferred alkoxylated surfactants can be selected from the classes of the nonionic condensates of alkyl phenols, nonionic ethoxylated alcohols, nonionic ethoxylated/propoxylated fatty alcohols, and mixtures thereof.
• nonionic alkoxylated alcohol surfactants being the condensation products of aliphatic alcohols with from 1 to 75 moles of alkylene oxide, in particular 50 or from 1 to 15 moles, preferably to 11 moles, particularly ethylene oxide and/or propylene oxide, are highly preferred nonionic surfactants.
• the alkyl chain of the aliphatic alcohol can either be straight or branched, primary or secondary, and generally contains from 6 to 22 carbon atoms.
• Particularly preferred are the condensation products of alcohols having an alkyl group containing from 8 to 20 carbon atoms with from 2 to 9 moles and in particular 5 or 7 moles, of ethylene oxide per mole of alcohol.
• Polyhydroxy fatty acid amides are highly preferred nonionic surfactant comprised by the composition, in particular those having the structural formula R 2 CONR 1 Z wherein: R 1 is H, C 1-18 , preferably C 1 -C 4 hydrocarbyl, 2-hydroxy ethyl, 2-hydroxy propyl, ethoxy, propoxy, or a mixture thereof, preferable C 1 -C 4 alkyl, more preferably C 1 or C 2 alkyl, most preferably C 1 alkyl (i.e., methyl); and R 2 is a C 5 -C 31 hydrocarbyl, preferably straight-chain C 5 -C 19 or C 7 -C 19 alkyl or alkenyl, more preferably straight-chain C 9 -C 17 alkyl or alkenyl, most preferably straight-chain C 11 -C 17 alkyl or alkenyl, or mixture thereof; and Z is a polyhydroxyhydrocarbyl having a linear hydrocarbyl chain with at least 3 hydroxyls directly connected to the
• any cationic detersive, preferably non-softening, surfactant is suitable for use in the cleaning system of the present invention.
• certain cationic surfactants as described herein after are more preferred.
• cationic alkoxylated surfactants and in particular, mono- and bis-alkoxylated quaternary amine surfactants with a C 6 -C 18 N-alkyl chain, such as of the general formula I: wherein R 1 is an alkyl or alkenyl moiety containing from 6 to 18 carbon atoms, preferably 6 to 16 carbon atoms, most preferably from 6 to 14 carbon atoms; R 2 and R 3 are each independently alkyl groups containing from one to three carbon atoms, preferably methyl, most preferably both R 2 and R 3 are methyl groups; R 4 is selected from the group consisting of hydrogen (preferred), methyl, ethyl, and mixtures thereof; X - is an anion such as chloride, bromide, methylsulfate, sulfate, and mixtures thereof, to provide electrical neutrality; A is a alkoxy group, especially a ethoxy, propoxy, butoxy group, and mixtures thereof; and p
• the cationic bis-alkoxylated amine surfactant preferably has the general formula II: wherein R 1 is an alkyl or alkenyl moiety containing from 8 to 18 carbon atoms, preferably 10 to 16 carbon atoms, most preferably from 10 to 14 carbon atoms; R 2 is an alkyl group containing from one to three carbon atoms, preferably methyl; R 3 and R 4 can vary independently and are selected from the group consisting of hydrogen (preferred), methyl, ethyl, and mixtures thereof; X - is an anion such as chloride, bromide, methylsulfate, sulfate, and mixtures thereof, sufficient to provide electrical neutrality.
• a and A' can vary independently and are each selected from the group consisting of C1-C4 alkoxy, especially ethoxy, (i.e., -CH 2 CH 2 O-), propoxy, butoxy, and mixtures thereof; p is from 1 to 30, preferably 1 to 4 and q is from 1 to 30, preferably 1 to 4, and most preferably both p and q are 1.
• cationic ester surfactants Another suitable group of cationic surfactants which can be used in the cleaning systems herein are cationic ester surfactants.
• Suitable cationic ester surfactants, including choline ester surfactants, have for example been disclosed in US Patents No.s 4,228,042, 4,239,660 and 4,260,529.
• Suitable amphoteric or zwitterionic detersive surfactants for use in the cleaning system herein include those which are known for use in hair softening or other personal softening cleansing. Concentration of such amphoteric detersive surfactants preferably ranges from 0.0% to 20%, preferably from 0.5% to 5% bu weight of the fabric treatment composition. Non-limiting examples of suitable zwitterionic or amphoteric surfactants are described in U.S. Pat. Nos. 5,104,646 (Bolich Jr. et al.), 5,106,609 (Bolich Jr. et al.).
• Amphoteric detersive surfactants suitable for use in the cleaning system of the present invention are well known in the art, and include those surfactants broadly described as derivatives of aliphatic secondary and tertiary amines in which the aliphatic radical can be straight or branched chain and wherein one of the aliphatic substituents contains from 8 to 18 carbon atoms and one contains an anionic group such as carboxy, sulfonate, sulfate, phosphate, or phosphonate.
• Suitable amphoteric detersive surfactants for use in the present invention include cocoamphoacetate, cocoamphodiacetate, lauroamphoacetate, lauroamphodiacetate, and mixtures thereof.
• Zwitterionic detersive surfactants suitable for use in the cleaning systems of the present invention are well known in the art, and include those surfactants broadly described as derivatives of aliphatic quaternary ammonium, phosphonium, and sulfonium compounds, in which the aliphatic radicals can be straight or branched chain, and wherein one of the aliphatic substituents contains from 8 to 18 carbon atoms and one contains an anionic group such as carboxy, sulfonate, sulfate, phosphate or phosphonate. Zwitterionics such as betaines are suitable for this invention.
• amine oxide surfactants having the formula: R(EO) x (PO) y (BO) z N(O)(CH 2 R') 2 .qH 2 O (I) are also suitable for incorporation within the compositions of the present invention.
• R is a relatively long-chain hydrocarbyl moiety which can be saturated or unsaturated, linear or branched, and can contain from 8 to 20, preferably from 10 to 16 carbon atoms, and is more preferably C12-C16 primary alkyl.
• R' is a short-chain moiety preferably selected from the group consisting of hydrogen, methyl, -CH 2 OH, and mixtures thereof.
• EO is ethyleneoxy
• PO propyleneneoxy
• BO is butyleneoxy.
• Amine oxide surfactants are illustrated by C 12-14 alkyldimethyl amine oxide.
• Non-limiting examples of other anionic, zwitterionic, amphoteric or optional additional surfactants suitable for use in the compositions are described in McCutcheon's, Emulsifiers and Detergents, 1989 Annual, published by M. C. Publishing Co., and U.S. Pat. Nos. 3,929,678; 2,658,072; 2,438,091; and 2,528,378.
• Mixtures of the above components can be made in any proportion.
• the second essential element of the fabric treatment compositions used in the present invention is a fabric softening system.
• the fabric softening system is present at levels of between 0.01% to 20%, more preferably between 0.1% to 15%, and most preferably between 0.5% to 10% by weight of the fabric treatment composition.
• the fabric softening system comprising at least one fabric softening active selected from the group consisting of (i) cationic ammonium-based fabric softening compounds comprising at least one carbonyl functionality; wherein the molar ratio of anionic surfactant to ammonium-based fabric softener is at least 3:1; (ii) cationic guar gums with a charge density between 0.2 meq/gm to 5.0 meq/gm; and (iii) mixtures thereof.
• Preferred quaternary ammonium fabric softening active compounds having the formula or the formula: wherein Q is a carbonyl unit having the formula: each R unit is independently hydrogen, C 1 -C 6 alkyl, C 1 -C 6 hydroxyalkyl, and mixtures thereof, preferably methyl or hydroxy alkyl; each R 1 unit is independently linear or branched C 11 -C 22 alkyl, linear or branched C 11 -C 22 alkenyl, and mixtures thereof, R 2 is hydrogen, C 1 -C 4 alkyl, C 1 -C 4 hydroxyalkyl, and mixtures thereof; X is an anion which is compatible with fabric softener actives and adjunct ingredients; the index m is from 1 to 4, preferably 2; the index n is from 1 to 4, preferably 2.
• An example of a preferred fabric softener active is a mixture of quaternized amines having the formula: wherein R is preferably methyl; R 1 is a linear or branched alkyl or alkenyl chain comprising at least 11 atoms, preferably at least 15 atoms.
• the unit -O 2 CR 1 represents a fatty acyl unit which is typically derived from a triglyceride source.
• the triglyceride source is preferably derived from tallow, partially hydrogenated tallow, lard, partially hydrogenated lard, vegetable oils and/or partially hydrogenated vegetable oils, such as, canola oil, safflower oil, peanut oil, sunflower oil, corn oil, soybean oil, tall oil, rice bran oil, etc. and mixtures of these oils.
• the preferred fabric softening actives of the present invention are the Diester and/or Diamide Quaternary Ammonium (DEQA) compounds, the diesters and diamides having the formula: wherein R, R 1 , X, and n are the same as defined herein above for formulas (1) and (2), and Q has the formula:
• DEQA Diester and/or Diamide Quaternary Ammonium
• the counterion, X (-) above can be any softener-compatible anion, preferably the anion of a strong acid, for example, chloride, bromide, methylsulfate, ethylsulfate, sulfate, nitrate and the like, more preferably chloride or methyl sulfate.
• the anion can also, but less preferably, carry a double charge in which case X (-) represents half a group.
• Tallow and canola oil are convenient and inexpensive sources of fatty acyl units which are suitable for use in the present invention as R 1 units.
• R 1 units The following are non-limiting examples of quaternary ammonium compounds suitable for use in the compositions of the present invention.
• tallowyl indicates the R 1 unit is derived from a tallow triglyceride source and is a mixture of fatty acyl units.
• canolyl refers to a mixture of fatty acyl units derived from canola oil.
• quaternary ammonium softening compounds are methylbis(tallowamidoethyl)(2-hydroxyethyl) ammonium methylsulfate and methylbis(hydrogenatedtallowamidoethyl)(2-hydroxyethyl) ammonium methylsulfate which are available from Witco Chemical Company under the trade names Varisoft® 222 and Varisoft® 110, respectively. Particularly preferred are N,N-di(canolyl-oxyethyl)-N,N-dimethyl ammonium chloride and N,N-di(canolyl-oxy-ethyl)-N-methyl, N-(2-hydroxyethyl) ammonium methyl sulfate.
• R units are preferably methyl, however, suitable fabric softener actives are described by replacing the term "methyl" in the above examples in Table I with the units: ethyl, ethoxy, propyl, propoxy, isopropyl, butyl, isobutyl and t-butyl.
• the counter ion, X in the examples of Table I can be suitably replaced by bromide, methyl sulfate, formate, sulfate, nitrate, and mixtures thereof.
• the anion, X is merely present as a counterion of the positively charged quaternary ammonium compounds. The scope of this invention is not considered limited to any particular anion.
• DEQA cationic scavenging agents described herein that can be used in the preparation of the composition herein and having desirable levels of unsaturation, and their syntheses, are described in WO 98/03 619 with good freeze/thaw recovery.
• Mixtures of actives of formula (1) and (2) may also be prepared.
• quaternary ammonium fabric softening compounds for use herein are diamino alkoxylated quaternary ammonium salts having the formula: wherein n is equal to 1 to 5; R 1 is a linear or branched alkyl or alkenyl chain comprising at least 11 atoms, preferably at least 15 atoms; R 2 and R 5 are independently selected from the group consisting of C 1 -C 4 alkyl, C 1 -C 4 hydroxyalkyl, and mixtures thereof; and A - is as defined above.
• DEQA diester or diamido quaternary ammonium fabric softening active compound
• Cationic guar gums can be present in the fabric softening system of the present invention.
• Guar gums are branched polysaccharides. They have a mannan backbone, a linear chain of 1,4-linked ⁇ -D-mannopyranosyl units, every other unit of which (on average) is substituted with a 1,6-linked ⁇ -D-galactopyranosyl unit. Like most polysaccharides, guar gum contains three free hydroxyl groups per sugar unit, which can be reacted with many chemicals.
• a commonly used procedure to make cationic guar gum includes: 1) hydroxypropyl guar is obtained by condensation of guar gum with propylene oxide; 2) cationic guar gum is formed by the reaction of hydroxypropyl guar with appropriate cationic agents.
• Commercially available cationic guar gums include N-Hance guar derivatives such as N-Hance 3196 and N-Hance 3000 from Hercules Incorporated of Wilmington, Delaware, Jaguar Excell and Jaguar C-13 from Rhodia of Aubervilliers, France.
• An ideal structure of a cationic guar gum is shown in the Structural Formula below.
• the molecular weight of cationic guar gum needs to be at least 10,000 and preferably at least 50,000.
• the degree of cationic substitution for use with the present invention should be in the range of 0.01 to 1.00 and preferably from 0.02 to 0.50.
• the charge density of the guar gums suitable for use in the compositions of the present invention is between 0.2 meq/gm to 5.0 meq/gm, preferably between 0.25 meq/mg to 3 meq/gm, and more preferably between 0.3 meq/gm to 2 meq/gm at the pH of intended use of the composition, which will generally range from pH 3 to pH 9, preferably between pH 4 and pH 8.
• the fabric treatment composition of the present invention is contained in the inner volume space of the pouch.
• the liquid fabric treatment composition is generally non-aqueous.
• the composition is non-aqueous if it contains less than 15% wt., preferably between 2% to 10% wt., more preferably between 3% and 8% wt., and most preferably between 3.5% and 6% by weight of the fabric treatment composition, of water. This is on basis of total water by weight of the total fabric treatment composition.
• the liquid composition can made by any method and can have any viscosity, typically depending on its ingredients.
• the liquid composition preferably has a viscosity of 0.0001 m 2 /s (100 centipoises) to 0.1 m 2 /s (100,000 centipoises), as measured at a rate of 20 s -1 , more preferably from 0.0002 m 2 /s (200 centipoises) to 0.05 m 2 /s (50,000 centipoises), even more preferably from 0.00025 m 2 /s (250 centipoises) to 0.01 m 2 /s (10,000 centipoises), and most preferably from 0.003 m 2 /s (300 centipoises) to 0.001 m 2 /s (1,000 centipoises).
• the liquid compositions herein can be Newtonian or non-Newtonian.
• the liquid composition preferably has a density of 0.8kg/l to 1.3kg/l, preferably around 1.0 to 1.1 kg/l.
• At least one builder is present. More preferably, at least one water-soluble builder is present, and even more preferably at least one fatty acid builder is present.
• the most preferred builder suitable for incorporation in the compositions of the present invention is citric acid.
• Preferred is also the presence of enzymes and preferred may also be to incorporate a bleaching agent, such as a preformed peroxyacid.
• the liquid composition comprises preferably a colorant or dye and/ or pearlescence agent.
• perfume especially from 5.5 to 9, more preferably 6 to 8
• buffering agents to maintain the pH preferably from 5.5 to 9, more preferably 6 to 8
• suds suppressors anti-wrinkling agent.
• an additional solvent which is preferably an organic solvent, more preferably selected from the group consisting of C1-C20 linear, branched, cyclic, saturated and/or unsaturated alcohols with one or more free hydroxy groups; amines, alkanolamines, and mixtures thereof.
• solvents are monoalcohols, diols, monoamine derivatives, glycerols, glycols, and mixtures thereof, such as ethanol, propanol, propandiol, monoethanolamin, glycerol, sorbitol, alkylene glycols, polyalkylene glycols, and mixtures thereof, and most preferred solvents are selected from 1,2-propandiol, 1.3-propandiol, glycerol, ethylene glycol, diethyleneglycol, and mixtures thereof.
• compositions used in the present invention comprise solvents at levels of from 0.1% to 90%, preferably of from 10% to 70%, more preferably of from 12% to 40% and most preferably of from 15% to 30% by weight of the fabric treatment composition.
• compositions in accordance with the present invention preferably contain a water-soluble builder compound, typically present in detergent compositions at levels of from 1% to 60% by weight, preferably from 3% to 40% by weight, most preferably from 5% to 25% by weight of the composition.
• Suitable water-soluble builder compounds include the water soluble monomeric carboxylates, or their acid forms, or homo or copolymeric polycarboxylic acids or their salts in which the polycarboxylic acid comprises at least two carboxylic radicals separated from each other by not more that two carbon atoms, and mixtures of any of the foregoing.
• Preferred builder compounds include citrate, tartrate, succinates, oxydissuccinates, carboxymethyloxysuccinate, nitrilotriacetate, and mixtures thereof.
• the compositions comprise from 2% to 40%, more preferably from 5% to 30%, and most preferably 10% to 25% by weight of the composition of a fatty acid or salt thereof.
• Preferred are in particular C 12 -C 18 saturated and/or unsaturated, linear and/or branched, fatty acids, but preferably mixtures of such fatty acids.
• mixtures of saturated and unsaturated fatty acids for example preferred is a mixture of rape seed-derived fatty acid and C 16 -C 18 topped whole cut fatty acids, or a mixture of rape seed-derived fatty acid and a tallow alcohol derived fatty acid, palmitic, oleic, fatty alkylsuccinic acids, and mixtures thereof.
• compositions of the invention may comprise phosphate-containing builder material.
• phosphate-containing builder material Preferably present at levels of from 2% to 40%, more preferably from 5% to 30%, more preferably from 10% to 25%.
• Suitable examples of water-soluble phosphate builders are the alkali metal tripolyphosphates, sodium, potassium and ammonium pyrophosphate, sodium and potassium and ammonium pyrophosphate, sodium and potassium orthophosphate, sodium polymeta/phosphate in which the degree of polymerization ranges from 6 to 21, and salts of phytic acid.
• compositions in accord with the present invention may contain a partially soluble or insoluble builder compound, typically present in detergent compositions at levels of from 0.5% to 60% by weight, preferably from 5% to 50% by weight, most preferably from 8% to 40% weight of the composition.
• compositions in accordance with the present invention preferably contain a structuring agent, typically present of from 0.1 % to 20%, preferably from 0.15% to 15%, more preferably from 0.2% to 5% by weight of the fabric treatment composition.
• the structuring agent serves to stabilize the fabric care compositions herein and to prevent the fabric treatment compositions herein from coagulating and/or creaming.
• the structuring agent is a crystalline, hydroxyl-containing structuring agent, more preferably still, a trihydroxystearin, hydrogenated oil or a variation thereof.
• the crystalline, hydroxyl-containing stabilizing agent is a nonlimiting example of an agent which forms a "thread-like structuring system.”
• "Thread-like Structuring System” as used herein means a system comprising one or more agents that are capable of providing a chemical network that reduces the tendency of materials with which they are combined to coalesce and/or phase split. Examples of the one or more agents include crystalline, hydroxyl-containing stabilizing agents and/or hydrogenated jojoba.
• the thread-like structuring system forms a fibrous or entangled threadlike network in-situ on cooling of the matrix.
• the thread-like structuring system has an average aspect ratio of from 1.5:1, preferably from at least 10:1, to 200:1.
• the thread-like structuring system can be made to have a viscosity of 2000 cstks or less at an intermediate shear range (5 s -1 to 50 s -1 ) which allows for the pouring of the composition out of a standard bottle, while the low shear viscosity of the product at 0.1 s -1 can be at least 2000 cstks but more preferably greater than 20,000 cstks.
• a process for the preparation of a thread-like structuring system is disclosed in WO 02/18528.
• hydroxyl-containing stabilizing agents can be fatty acid, fatty ester or fatty soap water-insoluble wax-like substance.
• the crystalline, hydroxyl-containing stabilizing agents in accordance with the present invention are preferably derivatives of castor oil, especially hydrogenated castor oil derivatives.
• castor oil especially hydrogenated castor oil derivatives.
• castor wax especially castor wax.
• the crystalline, hydroxyl-containing agent typically is selected from the group consisting of: wherein R 1 is -C(O)R 4 , R 2 is R 1 or H, R 3 is R 1 or H, and R 4 is independently C 10 -C 22 alkyl or alkenyl comprising at least one hydroxyl group; wherein: R 4 is as defined above in i); M is Na + , K + , Mg ++ or Al 3+ , or H; and iii) mixtures thereof.
• the crystalline, hydroxyl-containing stabilizing agent may have the formula: wherein:
• perfume components preferably at least one component comprising a coating agent and/ or carrier material, preferably organic polymer carrying the perfume or alumniosilicate carrying the perfume, or an encapsulate enclosing the perfume, for example starch or other cellulosic material encapsulate.
• a coating agent and/ or carrier material preferably organic polymer carrying the perfume or alumniosilicate carrying the perfume, or an encapsulate enclosing the perfume, for example starch or other cellulosic material encapsulate.
• the pouch compositions of the present invention comprise from 0.01 % to 4% of perfume, more preferably from 0.1 % to 2%.
• compositions herein may also optionally comprise from 0.005% to 10% by weight of a bleaching agent.
• the bleaching agent may be present as a perhydrate bleach, such as salts of percarbonates, particularly the sodium salts, and/ or organic peroxyacid bleach precursor, and/or transition metal bleach catalysts, especially those comprising Mn or Fe. It has been found that when the pouch or compartment is formed from a material with free hydroxy groups, such as PVA, the preferred bleaching agent comprises a percarbonate salt and is preferably free form any perborate salts or borate salts. It has been found that borates and perborates interact with these hydroxy-containing materials and reduce the dissolution of the materials and also result in reduced performance.
• Inorganic perhydrate salts are a preferred source of peroxide.
• examples of inorganic perhydrate salts include percarbonate, perphosphate, persulfate and persilicate salts.
• the inorganic perhydrate salts are normally the alkali metal salts. Alkali metal percarbonates, particularly sodium percarbonate are preferred perhydrates herein.
• the composition herein preferably comprises a peroxy acid or a precursor therefor (bleach activator), preferably comprising an organic peroxyacid bleach precursor. It may be preferred that the composition comprises at least two peroxy acid bleach precursors, preferably at least one hydrophobic peroxyacid bleach precursor and at least one hydrophilic peroxy acid bleach precursor, as defined herein.
• the production of the organic peroxyacid occurs then by an in-situ reaction of the precursor with a source of hydrogen peroxide.
• the hydrophobic peroxy acid bleach precursor preferably comprises a compound having a oxy-benzene sulphonate group, preferably NOBS, DOBS, LOBS and/ or NACA-OBS.
• the hydrophilic peroxy acid bleach precursor preferably comprises TAED.
• Amide substituted alkyl peroxyacid precursor compounds can be used herein. Suitable amide substituted bleach activator compounds are described in EP-A-0 170 386.
• the composition may contain a pre-formed organic peroxyacid.
• organic peroxyacids include diacyl and tetraacylperoxides, especially diperoxydodecanedioc acid, diperoxytetradecanedioc acid and diperoxyhexadecanedioc acid.
• diacyl and tetraacylperoxides especially diperoxydodecanedioc acid, diperoxytetradecanedioc acid and diperoxyhexadecanedioc acid.
• Mono- and diperazelaic acid, mono- and diperbrassylic acid and N-phthaloylaminoperoxicaproic acid are also suitable herein.
• the composition may comprise a suds suppresser at levels of less than 10%, preferably 0.001% to 10%, preferably from 0.01% to 8%, most preferably from 0.05% to 5%, by weight of the composition.
• the suds suppresser is either a soap, paraffin, wax, or any combination thereof. If the suds suppresser is a suds suppressing silicone, then the composition preferably comprises from 0.005% to 0.5% by weight a suds suppressing silicone.
• Suitable suds suppressing systems for use herein may comprise essentially any known antifoam compound, including for example silicone antifoam compounds and 2-alkyl alcanol antifoam compounds.
• Suitable antifoam compounds include the monocarboxylic fatty acids and soluble salts thereof, as also described as builders above. These materials are described in US Patent 2,954,347, issued September 27, 1960 to Wayne St. John.
• the monocarboxylic fatty acids, and salts thereof, for use as suds suppressor typically have hydrocarbyl chains of 10 to 24 carbon atoms, preferably 12 to 18 carbon atoms.
• Suitable salts include the alkali metal salts such as in particular sodium but also potassium salts.
• Another preferred ingredient useful in the compositions herein is one or more enzymes.
• Suitable enzymes include enzymes selected from the group consisting of peroxidases, proteases, gluco-amylases, amylases, xylanases, cellulases, lipases, phospholipases, esterases, cutinases, pectinases, keratanases, reductases, oxidases, phenoloxidases, lipoxygenases, ligninases, pullulanases, tannases, pentosanases, malanases, ⁇ -glucanases, arabinosidases, hyaluronidase, chondroitinase, dextranase, transferase, laccase, mannanase, xyloglucanases, or mixtures thereof.
• Detergent compositions generally comprise a cocktail of conventional applicable enzymes like protease, amylase, cellulase, lipase.
• Enzymes are generally incorporated in detergent compositions at levels of from 0.0001 % to 2%, preferably from 0.001 % to 0.2%, more preferably from 0.005% to 0.1 % pure enzyme by weight of the composition.
• the above-mentioned enzymes may be of any suitable origin, such as vegetable, animal, bacterial, fungal and yeast origin. Origin can further be mesophilic or extremophilic (psychrophilic, psychrotrophic, thermophilic, barophilic, alkalophilic, acidophilic, halophilic, etc.). Purified or non-purified forms of these enzymes may be used.
• the variants may be designed such that the compatibility of the enzyme to commonly encountered ingredients of such compositions is increased.
• the variant may be designed such that the optimal pH, bleach or chelant stability, catalytic activity and the like, of the enzyme variant is tailored to suit the particular cleaning application.
• enzyme stability in liquid detergents attention should be focused on amino acids sensitive to oxidation in the case of bleach stability and on surface charges for the surfactant compatibility.
• the isoelectric point of such enzymes may be modified by the substitution of some charged amino acids.
• the stability of the enzymes may be further enhanced by the creation of e.g. additional salt bridges and enforcing metal binding sites to increase chelant stability.
• enzymes might be chemically or enzymatically modified, e.g. PEG-ylation, cross-linking and/or can be immobilized, i.e. enzymes attached to a carrier can be applied.
• the enzyme to be incorporated in a detergent composition can be in any suitable form, e.g. liquid, encapsulate, prill, granulate or any other form according to the current state of the art.
• compositions herein may also optionally comprise from 0.005% to 10% by weight of organic polymeric compounds.
• Useful additional non-alkoxylated organic polymeric compounds for inclusion in the compositions herein include the water soluble organic homo- or co-polymeric polycarboxylic acids or their salts in which the polycarboxylic acid comprises at least two carboxyl radicals separated from each other by not more than two carbon atoms. Polymers of the latter type are disclosed in GB-A-1,596,756. Examples of such salts are polyacrylates of MWt 1000-5000 and their copolymers with maleic anhydride, such copolymers having a molecular weight of from 2000 to 100,000, especially 40,000 to 80,000.
• organic polymeric compounds suitable for incorporation in the compositions herein include cellulose derivatives.
• compositions herein may also comprise from 0.01% to 10 %, preferably from 0.05% to 0.5% by weight of polymeric dye transfer inhibiting agents.
• the polymeric dye transfer inhibiting agents are preferably selected from polyamine N-oxide polymers, copolymers of N-vinylpyrrolidone and N-vinylimidazole, polyvinylpyrrolidonepolymers or combinations thereof, whereby these polymers can be cross-linked polymers.
• compositions herein may also optionally comprise from 0.005% to 5% by weight of optical brighteners.
• Preferred brighteners include 4,4',-bis[(4-anilino-6-(N-2-bis-hydroxyethyl)-s-triazine-2-yl)amino]-2,2'-stilbenedisulfonic acid and disodium salt, commercially marketed under the tradename Tinopal-UNPA-GX by Ciba-Geigy Corporation; 4,4'-bis[(4-anilino-6-(N-2-hydroxyethyl-N-methylamino)-s-triazine-2-yl)amino]2,2'-stilbene disulfonic acid disodium salt, commercially marketed under the tradename Tinopal 5BM-GX by Ciba-Geigy Corporation; 4,4'-bis[(4-anilino-6-morphilino-s-triazine-2-yl)amino]2,2'-stilbene-disulfonic acid, sodium salt, commercially marketed under the tradename Tinopal-
• composition may optionally comprise one or more alkoxylated compounds having at least two alkoxylated amine, imine, amide or imide groups.
• alkoxylated compounds having at least two alkoxylated amine, imine, amide or imide groups.
• Preferred are compounds having at least two alkoxylated amine groups.
• the alkoxylation group may have one or more alkoxylates, typically more than one, thus forming a chain of alkoxylates, or polyalkoxylation group.
• the compound may have two alkoxylation groups or chain, preferably at least 4 or even at least 7 or even at least 10 or even at least 16.
• the alkoxylation groups are polyalkoxylation groups, (each independently) having an average alkoxylation degree of at least 5, more preferably at least 8, preferably at least 12, up to preferably 80 or even to 50 or even to 25.
• the (poly)alkoxylation is preferably a (poly)ethoxylation and/ or (poly)propoxylation.
• the alkoxylation group is a polyethoxylation group or polypropoxylation group, or a (poly)ethoxylation/ (poly)propoxyltion group.
• a polymer is a compound having 2 or more repeating monomer units forming a backbone.
• the alkoxylated polymer herein is preferably such that the alkoxylation groups are not part of the backbone of the polymer, but are alkoxylation groups of the amine, imine, amide or imide in the units forming the backbone, or are alkoxylation groups of other side-groups chemically bound to the backbone.
• Said alkoxylated compound is preferably a polyamide, polyimide or more preferably a polyamine or polyime compound, whereby these amide, imide, amine or imine units are present as backbone of the polymer, forming the chain of repeating units.
• these polymers have at least 3 or even 4 or even 5 amide, imide, amine or imine units.
• the backbone has also side-chains containing amide, imide, amine or imine groups, which may be alkoxylated.
• the composition herein comprises (by weight of the composition) from 0.5% to 15%, more preferably from 0.8% to 10%, more preferably form 1.5% to 8%, more preferably from 2.0% or even 2.5% or even 3% to 6% of said alkoxylated compound.
• the composition herein may comprise preferably mixtures of the specified compounds.
• ethoxylated poly(ethyleneimine) preferably having an average ethoxylationd degree per ethoxylation chain of 15 to 25, and a molecular weight of 1000-2000 dalton.
• ethoxylated tetraethylene pentaimines are also highly preferred.
• composition herein can comprise a chelating agent, for example, having two or more phosphonic acid or phosphonate groups, or two or more carboxylic acid or carboxylate groups, or mixtures thereof.
• chelating agent it is meant herein components which act to preferentially sequester (chelate) heavy metal ions, but these components may also have calcium and magnesium chelation capacity.
• Chelating agents are generally present at levels of from 1%, preferably from 2.5% from 3.5% or even 5.0% or even 7% and preferably up to 20% or even 15% or even 10% by weight of the composition herein.
• Highly suitable organic phosphonates herein are amino alkylene poly (alkylene phosphonates), alkali metal ethane 1-hydroxy bisphosphonates and nitrilo trimethylene phosphonates.
• Preferred among the above species are diethylene triamine penta (methylene phosphonate), ethylene diamine tri (methylene phosphonate) hexamethylene diamine tetra (methylene phosphonate) and hydroxy-ethylene 1,1 diphosphonate.
• Suitable chelating agents for use herein include nitrilotriacetic acid and polyaminocarboxylic acids such as ethylenediaminotetracetic acid, ethylenetriamine pentacetic acid, ethylenediamine disuccinic acid, ethylenediamine diglutaric acid, 2-hydroxypropylenediamine disuccinic acid or any salts thereof.
• Glycinamide-N,N'-disuccinic acid Glycinamide-N,N'-disuccinic acid (GADS), ethylenediamine-N-N'-diglutaric acid (EDDG) and 2-hydroxypropylenediamine-N-N'-disuccinic acid (HPDDS) are also suitable.
• Suitable chelating agents with two or more carboxylates or carboxylic acid groups include the acid or salt forms of succinic acid, malonic acid, (ethylenedioxy) diacetic acid, maleic acid, diglycolic acid, tartaric acid, tartronic acid and fumaric acid, as well as the ether carboxylates and the sulfinyl carboxylates.
• Chelants containing three carboxy groups include, in particular, the acids or salt forms of citrates, aconitrates and citraconates as well as succinate derivatives.
• Preferred carboxylate chelants are hydroxycarboxylates containing up to three carboxy groups per molecule, more particularly citrates and citric acids.
• Chelating agents containing four carboxy groups include the salts and acid forms of oxydisuccinates, 1,1,2,2-ethane tetracarboxylates, 1,1,3,3-propane tetracarboxylates and 1,1,2,3-propane tetracarboxylates, sulfosuccinate derivatives.
• At least one organo phosphonate or phosphonic acid and also at least one di- or tri-carboxylate or carboxylic acid is present.
• At least fumaric acid (or salt) and citric acid (or salt) and one or more phosphonates are present.
• Preferred salts are sodium salts.
• the composition comprises, in addition to water, a plasticiser for the water-soluble pouch material, for example one of the plasticisers described above, for example glycerol.
• a plasticiser for the water-soluble pouch material for example one of the plasticisers described above, for example glycerol.
• Such plasticisers can have the dual purpose of being a solvent for the other ingredients of the composition and a plasticiser for the pouch material.
• hydrotrope Another highly preferred optional ingredient is a hydrotrope. It has been found that the inclusion of a hydrotrope in the present pouch compositions can further improve dissolution.
• a hydrotrope is a substance with the ability to increase the solubility of certain slightly soluble organic compounds. A description of hydrotropes for use herein can be found in Surfactant Science, Vol. 67 "Liquid Detergents", 1997 in Chapter 2 entitled “Hydrotropy”.
• compositions herein comprise from 0.01% to 15%, more preferably from 0.1% to 10%, even more preferably from 0.25% to 7%, even more preferably still from 0.5% to 5%, by weight of composition, of hydrotrope.
• Preferred hydrotropes are selected from sodium cumene sulphonate, sodium xylene sulphonate, sodium naphthalene sulphonate, sodium p-toluene sulphonate, and mixtures thereof. Especially preferred is sodium cumene sulphonate. While the sodium form of the hydrotrope is preferred, the potassium, ammonium, alkanolammonium, and/or C 2 -C 4 alkyl substituted ammonium forms can also be used.
• compositions of the present invention may optionally comprise additional fabric softening actives.
• additional softeners can be present in an amount of from 0.1% to 20%, preferably between 1% to 15%, and more preferably between 1.5% to 10% by weight of the fabric treatment composition.
• Fabric softening clays can optionally be present in the fabric softening system of the present invention as additional fabric softening materials.
• Preferred clays are of the smectite type.
• Smectite type clays are widely used as fabric softening ingredients in detergent compositions. Most of these clays have a cation exchange capacity of at least 50 meq/100g.
• Smectite clays can be described as three-layer expandable materials, consisting of alumino-silicates or magnesium silicates.
• smectite-type clays There are two distinct classes of smectite-type clays; in the first, aluminium oxide is present in the silicate crystal lattice, in the second class of smectites, magnesium oxide is present in the silicate crystal lattice.
• the general formulas of these smectites are Al 2 (Si 2 O 5 ) 2 (OH) 2 and Mg 3 (Si 2 O 5 )(OH) 2 , for the aluminium and magnesium oxide type clay, respectively.
• the range of the water of hydration can vary with the processing to which the clay has been subjected.
• atom substitution by iron and magnesium can occur within the crystal lattice of the smectites, while metal cations such as Na + , Ca 2+ , as well as H + can be co-present in the water of hydration to provide electrical neutrality.
• clays on the basis of one cation predominantly or exclusively absorbed.
• a sodium clay is one in which the absorbed cation is predominately sodium.
• Such absorbed cations can become involved in equilibrium exchange reactions with cations present in aqueous solutions.
• one equivalent weight of solution cation replaces an equivalent of sodium, for example, and it is customary to measure clay cation exchange capacity in terms of milliequivalents per 100g of clay (meq/100g).
• the cation exchange capacity of clays can be measured in several ways, including electrodialysis, by exchange with ammonium ion followed by titration, or by a methylene blue procedure, all as set forth in Grimshaw, The Chemistry and Physics of Clays, Interscience Publisher, Inc. pp.264 - 265 (1971).
• the cation exchange capacity of a clay mineral relates to such factors as the expandable properties of the clay, the charge of the clay, which in turn is determinated at least in part by the lattice structure.
• the ion exchange capacity of clays varies widely in the range from 2 meq/100g for kaolinites to 150 meq/100g and greater for certain clays of the montmorillonite variety.
• Illite clays have an ion exchange capacity somewhere in the lower portion of the range, c. 26 mew/100g for an average illite clay.
• illite and kaolinite clays are not useful in the fabric softening system of the fabric treatment compositions of the present invention. Indeed such illite and kaolinite clays constitute a major component of clay soils.
• smectites such as nontronite having an ion exchange capacity of approximately 50 meq/100g; saponite, which has an ion exchange capacity greater than 70 meq/100g, have been found to be useful fabric softening actives in the fabric softening system of the present invention.
• the smectite clays commonly used for this purpose herein are all commercially available. Such clays include, for example, montmorillonite, volchonskoite, nontronite, hectorite, paonite, sauconite, and vermiculite.
• the clays herein are available under commercial names such as "fooler clay” (clay found in a relatively thin vein above the main bentonite or monmorillonite veins in the Black Hills) and various tradenames such as Thixogel #1 (also, “Thixo-Jell”) and Gelwhite GP from Georgia Kaolin Co.
• Preferred for use herein are the montmorrillonite clays having an ion exchange capacity of 50 to 100 meq/10g which corresponds to ca. 0.2 to 0.6 layer charge.
• the value of (x+y) is the layer charge of the hectorite clay.
• Such hectorite clays are preferably selected on the basis of their layer charge properties, i.e. at least 50% is in the range of from 0.23 to 0.31. More suitable are hectorite clays of natural origin having a layer charge distribution such that at least 65% is in the range of from 0.23 to 0.31.
• the hectorite clays suitable in the present composition should preferably be sodium clays, for better softening activity.
• Sodium clays are either naturally occurring, or are naturally-occuring calcium-clays which have been treated so as to convert them to sodium-clays. If calcium-clays are used in the present compositions, a salt of sodium can be added to the compositions in order to convert the calcium clay to a sodium clay. Preferably, such a salt is sodium carbonate, typically added at levels of up to 5% of the total amount of clay.
• hectorite clays suitable for the present compositions include Bentone EW and Macaliod, from NL Chemicals, NJ, US, and hectorites from Industrial Mineral Ventures.
• Another preferred clay is an organophilic clay, preferably a smectite clay, whereby at least 30% or even at least 40% or preferably at least 50% or even at least 60% of the exchangeable cations is replaced by a, preferably long-chain, organic cations.
• organophilic clay preferably a smectite clay, whereby at least 30% or even at least 40% or preferably at least 50% or even at least 60% of the exchangeable cations is replaced by a, preferably long-chain, organic cations.
• Such clays are also referred to as hydrophobic clays.
• organophilic smectite clay Whilst the organophilic smectite clay provides excellent softening benefit, they can increase the viscosity of the liquid compositions. Therefore, it will depend on the viscosity requirements of the composition, how much of these organophlic clays can be used.
• organophilic clays are formed prior to incorporation into the detergent composition.
• the cations, or part thereof, of the normal smectite clays are replaced by the long-chain organic cations to form the organophilic smectite clays herein, prior to further processing of the material to form the detergents of the invention.
• the organophilic clay is preferably in the form of a platelet or lath-shaped particle.
• the ratio of the width to the length of such a platelet is at least 1:2, preferably at least 1:4 or even at least 1:6 or even at least 1:8.
• a long-chain organic cation can be any compound which comprises at least one chain having at least 6 carbon atoms, but typically at least 10 carbon atoms, preferably at least 12 carbon atoms, or in certain embodiments of the invention, at least 16 or even at least 18 carbon atoms. Preferred long-chain organic cations are described hereinafter.
• Preferred organophilic clays herein clay are smectite clays, preferably hectorite clays and/ or montmorillonite clays containing one or more organic cations of formulae: where R 1 represents an organic radical selected from the group consiting of R 7 , R 7 -CO-O-(CH 2 ) n , or R 7 -CO-NR 8 -, and mixtures thereof, in which R 7 is an alkyl, alkenyl or alkylaryl group with 12 to 22 carbon atoms, whereby R 8 is hydrogen, C 1 -C 4 alkyl, alkenyl or hydroxyalkyl, preferably -CH 3 or -C 2 H 5 or -H ; n is an integer, preferably equal to 2 or 3; R 2 represents an organic radical selected from the group consiting of R 1 or C 1 -C 4 alkyl, alkenyl or hydroxyalkyl, preferably -CH 3 or -CH 2 CH 2 OH; R 3 and R
• Highly preferred cations are quaternary ammonium cations having two C 16 -C 28 or even C 16 -C 24 alkyl chains.
• Highly preferred are one or more organic cations which have one or preferably two alkyl groups derived from natural fatty alcohols, the cations preferably being selected from the group consisting of dicocoyl methyl benzyl ammonium, dicocoyl ethyl benzyl ammonium, dicocoyl dimethyl ammonium, dicocoyl diethyl ammonium; more preferably ditallow diethyl ammonium, ditallow ethyl benzyl ammonium; more preferably ditallow dimethyl ammonium, ditallow methyl benzyl ammonium, and mixtures thereof. It may be highly preferred that mixtures of organic cations are present.
• organophilic clays as available from Rheox/Elementis, such as Bentone SD-1 and Bentone SD-3, which are registered trademarks of Rheox/Elementis.
• Clays are well known in the art for their fabric softening performance. In general, clays are usually processed as aqueous suspensions. However, the use of aqueous suspensions of fabric softening clays is not acceptable when the final composition is surrounded by a water-soluble pouch, because the water content present would lead at least partly to an early and therefore unwanted dissolution of the pouch material, i.e. before the consumer places the pouch in the washing machine, and therefore resulting in loss of treatment composition available for the laundry cycle and/or causing a mess in the consumers home. In order to overcome this technical problem, the present invention suggests adding clays as pure compounds or as premixes. These premixes comprise the clay and a solvent, preferably a non-aqueous solvent.
• the solvent is preferably an organic solvent, more preferably the organic solvent is selected from the group consisting of C1-C20 linear, branched, cyclic, saturated or unsaturated alcohols with one or more free hydroxy groups; amines, alkanolamines; and mixtures thereof.
• solvents include monoalcohols, diols, monoamine derivatives, glycerols, glycols, and mixtures thereof, such as ethanol, propanol, propandiol, monoethanolamin, glycerol, sorbitol, alkylene glycols, polyalkylene glycols, and mixtures thereof, and most preferred solvents are selected from the group consisting of 1,2-propandiol, 1.3-propandiol, glycerol, ethylene glycol, diethyleneglycol, and mixtures thereof.
• premixes comprising fabric softening clays and solvents are utilized in order to overcome process problems in terms of proper dispersion or dissolution of all ingredients throughout the composition.
• Uncharged, neutral fabric softening silicones can optionally be present in the fabric softening system of the present invention as additional fabric softening materials.
• silicone polymers are disclosed in "Silicone Surfactants, Editor: R. M. Hill, Surfactant Science Series, Vol. 86, Marcel Dekker, Inc., 1999".
• the silicone polymer is selected from the group consisting of nonionic nitrogen-free silicone polymers having the formulae (I) to (III): R 2 ⁇ (R 1 ) 2 SiO ⁇ [(R 1 ) 2 SiO] a ⁇ [(R 1 )(R 2 )SiO] b ⁇ Si(R 1 ) 2 ⁇ R 2 and mixtures thereof, wherein each R 1 is independently selected from the group consisting of linear, branched or cyclic substituted or unsubstituted alkyl groups having from 1 to 20 carbon atoms; linear, branched or cyclic substituted or unsubstituted alkenyl groups having from 2 to 20 carbon atoms; substituted or unsubstituted aryl groups having from 6 to 20 carbon atoms; substituted or unsubstituted alkylaryl, substituted or unsubstituted arylalkyl and substituted or unsubstituted arylalkenyl groups having from 7 to 20 carbon
• the nitrogen-free silicone polymer is selected from the group consisting of linear nonionic nitrogen-free silicone polymers having the formulae (II) to (III) as above, wherein R 1 is selected from the group consisting of methyl, phenyl, phenylalkyl, and mixtures thereof; wherein R 2 is selected from the group consisting of methyl, phenyl, phenylalkyl, and mixtures thereof; and from the group having the general formula (IV), defined as above, and mixtures thereof; wherein R 3 is defined as above and wherein the index w has the value as such that the viscosity of the nitrogen-free silicone polymer of formula (III) is between 0.01 m 2 /s (10,000 centistokes) and 0.8 m 2 /s (800,000 centistokes); a is from 1 to 30, b is from 1 to 30, n is from 3 to 5, total c is from 6 to 100, total d is from 0 to 3, and total c + d is from 7 to 100
• the nitrogen-free silicone polymer is selected from the group consisting of linear nonionic nitrogen-free silicone polymers having the formula (III) as above, wherein R 1 is methyl and wherein the index w has the value as such that the viscosity of the nitrogen-free silicone polymer of formula (III) is between 0.06 m 2 /s (60,000 centistokes) and 0.7 m 2 /s (700,000 centistokes) and more preferably between 0.1 m 2 /s (100,000 centistokes) and 0.48 m 2 /s (480,000 centistokes), and mixtures thereof.
• R contains the elements carbon and hydrogen only.
• substituted means that R comprises carbon and hydrogen and one or more heteroatoms selected from the group consisting of halogen (fluoro, chloro, bromo, iodo), oxygen, sulfur, phosphor, and/or one or more functional groups such as alkyl ethers, carboxylgrops, carboxylalkyl groups, hydroxy groups, hydroxyalkyl groups; and combinations thereof.
• Silicones are well known in the art for their fabric softening performance. Usually, these silicones are added as emulsions in water. As states above for the fabric softening clays, the use of aqueous emulsions of fabric softening silicones is not acceptable when the final composition is to be placed in water-soluble pouches.
• the present invention suggest adding the fabric softening silicones suitable for use in the present invention either as a premix comprising the silicone and a solvent, or adding the silicones as pure compounds without any solvent. When the fabric softening silicones are added as a premix, the premix is most likely a slurry or dispersion or suspension or emulsion of the silicone in the solvent.
• the solvent is preferably non-aqueous solvent, more preferably an organic solvent, and even more preferably selected from the group consisting of C1-C20 linear, branched, cyclic, saturated and/or unsaturated alcohols with one or more free hydroxy groups; amines, alkanolamines, and mixtures thereof.
• Preferred solvents are monoalcohols, diols, monoamine derivatives, glycerols, glycols, and mixtures thereof, such as ethanol, propanol, propandiol, monoethanolamin, glycerol, sorbitol, alkylene glycols, polyalkylene glycols, and mixtures thereof.
• Most preferred solvents are selected from the group consisting of 1,2-propandiol, 1.3-propandiol, glycerol, ethylene glycol, diethyleneglycol, and mixtures thereof.
• premixes comprising fabric softening silicones and solvents are utilized in order to overcome process problems in terms of proper dispersion or dissolution of all ingredients throughout the composition.
• Non-limiting examples of nitrogen-free silicone polymers of fomula (II) are the Silwet® compounds which are available from OSI Specialties Inc., a Division of Witco, Danbury, Connecticut.
• Non-limiting examples of nitrogen-free silicone polymers of fomula (I) and (III) are the Silicone 200 Fluid®-series from Dow Corning.
• Cationic silicone polymers can optionally be present in the fabric softening system of the present invention as additional fabric softening materials, in addition to a cationic guar gum or in addition to a cationic guar gum and an ammonium-based fabric softening agent as fabric softening agents.
• Suitable cationic silicones polymers are disclosed in the Applicant's co-pending case WO 02/18 528.
• Cationic silicones are well known in the art for their fabric softening performance. Usually, these cationic silicones are added as emulsions in water. As states above for the fabric softening clays, the use of aqueous emulsions of fabric softening cationic silicones is not acceptable when the final composition is to be placed in water-soluble pouches. In order to overcome this technical problem, the present invention suggest adding the fabric softening cationic silicones suitable for use in the present invention either as a premix comprising the cationic silicone and a solvent, or adding the cationic silicones as pure compounds without any solvent.
• the premix is most likely a slurry or dispersion or suspension or emulsion of the silicone in the solvent.
• the solvent is preferably non-aqueous solvent, more preferably an organic solvent, and even more preferably selected from the group consisting of C1-C20 linear, branched, cyclic, saturated and/or unsaturated alcohols with one or more free hydroxy groups; amines, alkanolamines, and mixtures thereof.
• Preferred solvents are monoalcohols, diols, monoamine derivatives, glycerols, glycols, and mixtures thereof, such as ethanol, propanol, propandiol, monoethanolamin, glycerol, sorbitol, alkylene glycols, polyalkylene glycols, and mixtures thereof.
• Most preferred solvents are selected from the group consisting of 1,2-propandiol, 1.3-propandiol, glycerol, ethylene glycol, diethyleneglycol, and mixtures thereof.
• premixes comprising fabric softening cationic silicones and solvents are utilized in order to overcome process problems in terms of proper dispersion or dissolution of all ingredients throughout the composition.
• compositions herein include colours, opacifiers, anti-oxidants, bactericides, neutralizing agents, buffering agents, phase regulants, thickeners and filler salts, with sodium sulfate being a preferred filler salt.
• the unit dose products of the present invention are used for cleaning and for softening of laundry.
• the unit dose product is added to the dispensing drawer, or alternatively to the drum, of an automatic washing machine.
• the pouch dissolves or disintegrates in water to deliver the detergent ingredients to the washing cycle.
• the unit dose products comprises all of the detergent ingredients of fabric cleaning system and all of the fabric softening ingredients used in the fabric treatment application during the wash cycle. Although it may be preferred that some detergent ingredients are not included within the pouch and are added to the washing cycle separately.
• one or more fabric treatment compositions other than the compositions held by the pouch can be used during the laundering process, such that said composition is used as a pre-treatment, main-treatment, post-treatment or a combination thereof during such a laundering process.
• the unit dose products of the present invention provide fabric treatment compositions suitable for low and high wash temperatures (e.g., 5°C to below 40°C for low temperatures and from 40°C to 95°C for high temperatures), low and high water levels (e.g., as in crease cycles for low water levels and as in wool cycles for high water levels), short and long washing times (e.g., 5 min. to below 50 min. for short washing times, and from 50 min. to 180 min. for long washing times) and the presence of small and large amounts of laundry (for example when the washing machine is "stuffed" with laundry).
• low and high wash temperatures e.g., 5°C to below 40°C for low temperatures and from 40°C to 95°C for high temperatures
• low and high water levels e.g., as in crease cycles for low water levels and as in wool cycles for high water levels
• short and long washing times e.g., 5 min. to below 50 min. for short washing times, and from 50 min. to 180 min. for long washing times
• the fabric treatment compositions used in the present invention can be prepared in any suitable manner and can, in general, involve any order of mixing or addition. However, there is a preferred way to make such compositions.
• the first step involves the preparation of the fabric cleaning system by combining all fabric cleaning ingredients in any suitable manner.
• the second step involves the preparation of the fabric softening system by combining all fabric softening ingredients in any suitable manner.
• the third step involves the combination of the fabric softening system and of the fabric cleaning system.
• the fabric softening system is typically added as a slurry, dispersion, suspension or emulsion of the fabric softener active in an appropriate solvent to the fabric cleaning system or vice versa.
• This process for preparing the fabric treatment composition of the present invention is preferably carried out using conventional high-shear mixing means. This ensures proper dispersion or dissolution of all ingredients throughout the final composition.
• Liquid compositions especially liquid detergent compositions in accordance with the invention preferably comprise a stabilizer, especially preferred being trihydroxystearin or hydrogenated castor oil, for example the type commercially available as Thixcin®.
• a stabilizer is to be added to the present compositions, it is preferably introduced as a separate stabilizer premix with one or more of the adjuncts, or non-silicone components, of the composition.
• the pouches can be made and filled in any conventional manner as disclosed in , for example, WO 02 / 08380 A1; WO 01 / 85 898 1; WO 02 / 08 376 A1; WO 01 / 79 417 A1; and WO 01 / 83 661 A1.
• unit dose products of the present invention demonstrate very good cleaning performance and very good fabric softening performance. Additionally, it has been found that the unit dose products of the present invention demonstrate better solubility and/or lower residues formation.
• anionic surfactant forms an ion-pair complex with one equivalent of cationic softener.
• a molar ratio of anionic surfactant to ammonium-based fabric softener of at least 2:1 should be sufficient (one equivalent of the anionic surfactant forms a ion-ion-pair complex with the cationic ammonium-based fabric softener, wherein the second equivalent would be available to do the cleaning), it has been found that an excess of at least one additional equivalent of anionic surfactant is needed.
• the molar ratio of anionic surfactant to ammonium-based fabric softener has to be at least 3:1, so that there is at least one equivalent of anionic surfactant left to perform as fabric cleaning agent.
• the ion-pair complex of anionic surfactant and fabric softener still performs as a fabric softener, so that the fabric treatment compositions of the present invention provide both a fabric cleaning benefit and a fabric softening benefit.
• the fabric cleaning benefits is provided through the cleaning system, e.g. through the anionic surfactant present and additionally also through additional further surfactants present, e.g. nonionic, cationic, zwitterionic and amphoteric surfactants.
• the fabric softening benefit is provided through the fabric softening system comprising either a cationic ammonium-based fabric softener or a cationic guar gum or mixtures thereof.
• a piece of plastic is placed in a mould to act as a false bottom.
• the mould consists of a cylindrical shape and has a diameter of 45mm and a depth of 25mm.
• a 1 mm thick layer of rubber is present around the edges of the mould.
• the mould has some holes in the mould material to allow a vacuum to be applied. With the false bottom in place the depth of the mould is 12mm.
• a piece of Monosol M-8630 film is placed on top of this mould and fixed in place. A vacuum is applied to pull the film into the mould and pull the film flush with the inner surface of the mould and the false bottom. 50ml of the liquid fabric treatment composition is poured into the mould.
• a second piece of Monosol M-8630 film is placed over the top of the mould with the liquid component and sealed to the first piece of film by applying an annular piece of flat metal of an inner diameter of 46mm and heating that metal under moderate pressure onto the ring of rubber at the edge of the mould to heat-seal the two pieces of film together to form a compartment comprising the liquid component.
• the metal ring is typically heated to a temperature of from 135°C to 150°C and applied for up to 5 seconds.
• Example II to XI all provide excellent fabric cleaning and fabric softening performance when added to the drum of an automatic washing machine wherein fabric are there and thereinafter laundered in conventional manner.

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• 2002
  • 2002-12-19 EP EP02447258A patent/EP1431381A1/de not_active Withdrawn
• 2003
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  • 2003-10-15 ES ES03447251T patent/ES2261909T3/es not_active Expired - Lifetime
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