WO2004022686A1 - Utilisation de celluloses cationiques favorisant l'administration d'agents de soin pour tissus - Google Patents

Utilisation de celluloses cationiques favorisant l'administration d'agents de soin pour tissus Download PDF

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Publication number
WO2004022686A1
WO2004022686A1 PCT/US2003/028421 US0328421W WO2004022686A1 WO 2004022686 A1 WO2004022686 A1 WO 2004022686A1 US 0328421 W US0328421 W US 0328421W WO 2004022686 A1 WO2004022686 A1 WO 2004022686A1
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WIPO (PCT)
Prior art keywords
fabric care
care benefit
water insoluble
mixtures
mixture
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PCT/US2003/028421
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English (en)
Inventor
Jiping Wang
Rajan Keshav Panandiker
Paul Francis Kindel
Mary Ruth Leyendecker
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The Procter & Gamble Company
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First worldwide family litigation filed litigation Critical https://patents.darts-ip.com/?family=31981196&utm_source=google_patent&utm_medium=platform_link&utm_campaign=public_patent_search&patent=WO2004022686(A1) "Global patent litigation dataset” by Darts-ip is licensed under a Creative Commons Attribution 4.0 International License.
Priority claimed from US10/375,792 external-priority patent/US6897190B2/en
Application filed by The Procter & Gamble Company filed Critical The Procter & Gamble Company
Priority to CA002495117A priority Critical patent/CA2495117A1/fr
Priority to EP03752219A priority patent/EP1537197B1/fr
Priority to BR0314147-0A priority patent/BR0314147A/pt
Priority to AU2003270521A priority patent/AU2003270521A1/en
Priority to MXPA05002611A priority patent/MXPA05002611A/es
Priority to JP2004534811A priority patent/JP4145874B2/ja
Priority to DE60319845T priority patent/DE60319845T2/de
Publication of WO2004022686A1 publication Critical patent/WO2004022686A1/fr

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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
    • C11D3/37—Polymers
    • C11D3/3703—Macromolecular compounds obtained otherwise than by reactions only involving carbon-to-carbon unsaturated bonds
    • C11D3/373—Macromolecular compounds obtained otherwise than by reactions only involving carbon-to-carbon unsaturated bonds containing silicones
    • C11D3/3742—Nitrogen containing silicones
    • 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
    • C11D3/00—Other compounding ingredients of detergent compositions covered in group C11D1/00
    • C11D3/16—Organic compounds
    • C11D3/37—Polymers
    • C11D3/3703—Macromolecular compounds obtained otherwise than by reactions only involving carbon-to-carbon unsaturated bonds
    • C11D3/373—Macromolecular compounds obtained otherwise than by reactions only involving carbon-to-carbon unsaturated bonds containing silicones
    • 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
    • C11D3/37—Polymers
    • C11D3/3746—Macromolecular compounds obtained by reactions only involving carbon-to-carbon unsaturated bonds
    • C11D3/3749—Polyolefins; Halogenated polyolefins; Natural or synthetic rubber; Polyarylolefins or halogenated polyarylolefins
    • 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
    • C11D3/37—Polymers
    • C11D3/3746—Macromolecular compounds obtained by reactions only involving carbon-to-carbon unsaturated bonds
    • C11D3/3757—(Co)polymerised carboxylic acids, -anhydrides, -esters in solid and liquid 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
    • C11D3/16—Organic compounds
    • C11D3/37—Polymers
    • C11D3/3788—Graft polymers
    • 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
    • C11D7/00—Compositions of detergents based essentially on non-surface-active compounds
    • C11D7/22—Organic compounds
    • C11D7/32—Organic compounds containing nitrogen
    • C11D7/329—Carbohydrate or derivatives thereof

Definitions

  • the present invention relates to the use of cationic celluloses to enhance deposition of water insoluble fabric care benefit agents such as water insoluble silicone derivatives during laundering.
  • Laundering textiles is a necessity in order to remove stains, odors and soils.
  • textiles can undergo mechanical and chemical damage which can result in fabric wrinkles, color fading, dye transfer, pills/fuzz, fabric wear, fiber deterioration, stiffness, and other undesirable consumer issues. Therefore, many laundry products such as detergents, fabric conditioners, and other wash, rinse, and dryer added products, frequently include one or more fabric care benefit agents that are added in an attempt to reduce or prevent these consumer issues.
  • fabric care benefit agents often provide limited benefits due to poor delivery efficiency on the fabrics or textiles during the laundering process.
  • the affinity between these fabric care agents and fabrics/garments is typically very limited due to the lack of natural attractive forces between the fabric care agents and the fabrics. This is because most fabric care agents used in laundry products are formulated to be anionic or nonionic in order to avoid interaction with anionic surfactants which might lead to potential cleaning negatives. Since most textile fibers such as cotton, wool, silk, nylon, and the like carry a slightly anionic charge in the laundry solution, there are repulsive instead of attractive forces between the fabric care agent and the fabric resulting in poor delivery efficiency.
  • water insoluble fabric care benefit agents examples of which include but are not limited to, water insoluble silicone derivatives and the like. Due to their water insolubility, water insoluble fabric care benefit agents are generally incorporated into laundry product formulations in some type of water stable form such as an emulsion, a latex, a dispersion, a suspension, or the like. When added to the laundry product in a water stable form, the water insoluble fabric care benefit agent becomes even more stable in solution. This is due to the existence of large amounts of surfactant that are present in laundry products.
  • the surfactant in the laundry products tends to act as an emulsifying agent, dispersion agent, suspension agent, or the like thereby resulting in the further stabilization of the emulsion, dispersion, and/or suspension containing the water insoluble fabric care benefit agent.
  • the affinity of the water insoluble fabric care benefit agent for the fabric is severely limited.
  • the majority of the water insoluble fabric care benefit agent tends to stay in solution wherein it is discarded with the wash solution thereby limiting the amount of benefit agent available for deposition on the fabric.
  • the laundry products of the present invention comprise at least one water insoluble fabric care benefit agent and at least one cationic cellulose delivery enhancing agent or deposition aid.
  • laundry products of the present invention improve the fabric delivery efficiency of water insoluble fabric care benefit agents that are incorporated therein by the inclusion of the cationic cellulose delivery agents of the present invention. It has surprisingly been found that by using cationic celluloses as delivery enhancing agents, the delivery of the water insoluble fabric care benefit agent to the fabric is significantly enhanced, which would not otherwise be possible.
  • the cationic celluloses may provide fabric care benefits by themselves, an amount of the cationic celluloses needed to deliver significant performance benefits is much larger than an amount of the cationic celluloses needed as a delivery enhancing agent.
  • large amounts of cationic celluloses often have a negative affect on cleaning performance. The cleaning negative caused by the large amount of cationic celluloses will normally prohibit their application in laundry detergent embodiments as the benefit agents alone.
  • the level of the cationic cellulose as the delivery enhancing agent the impact on cleaning is normally very limited.
  • the addition of the cationic celluloses of the present invention into laundry products may provide significant improvement in the delivery/deposition of the water insoluble fabric care benefit agent on the fabric versus utilizing the water insoluble fabric care benefit agent alone.
  • a laundry detergent containing cationic celluloses and the fabric care benefit agent are added in the washer, delivery/deposition enhancements of the water insoluble fabric care benefit agent on fabric of as much as 5 to 10 times the normal amount of benefit agent alone are observed.
  • the delivery/deposition enhancements may be accomplished by mixing the cationic cellulose and the fabric care benefit agent together as a laundry additive of a fabric care composite or by formulating these two ingredients into laundry detergent or other laundry products.
  • the water insoluble benefit agents useful herein include water insoluble silicone derivatives.
  • the water insoluble fabric care benefit agent preferably has a particle size of from about 1 nm to 100 um.
  • the present invention also comprises a detergent or fabric softener composition wherein the composition comprises: a. from about 1-80 wt% of an anionic, cationic, nonionic, amphoteric, zwitterionic surfactant or a combination thereof; b. from about 0.1- 10 wt% of a water insoluble benefit agent wherein said water insoluble fabric care benefit agent is a water insoluble silicone derivative, or a mixture thereof; and c. from about 0.01- 2% of a cationic cellulose.
  • the ratio of the delivery enhancing agent to the fabric care benefit agent is from about 1 : 50 to about 1 :1.
  • the present invention relates to the use of cationic celluloses to enhance deposition of water insoluble fabric care benefit agents including water insoluble silicone derivatives during laundering.
  • utilizing the cationic cellulose delivery enhancing agents of the present invention allows for improved delivery of the water insoluble fabric care benefit agent to the fabric so as to provide enhanced fabric softening, color protection, pill/fuzz reduction, anti-abrasion, anti-wrinkle, and other such benefits to garments and textiles.
  • the cationic cellulose, called the delivery enhancing agent, and the water insoluble fabric care benefit agent of the present invention may be mixed together prior to formulating in, adding to, or using in conjunction with a laundry product composition.
  • the two components may be formulated into laundry products separated with different orders of addition.
  • the two components of the present invention may also be mixed together in situ after addition to the laundry product composition. Additionally, the two components of the present invention may be applied directly to the fabric together or separately.
  • the deposition of the water insoluble fabric care benefit agent on the fabric is significantly improved and in some instances doubled, (i.e.; utilizing the delivery enhancing agent of the present invention may increase the deposition of the water insoluble fabric care benefit agent on the fabric by potentially about 100% or more compared with using the water insoluble fabric care benefit agent alone).
  • deposition on the fabric will increase by at least about 200%. Since the fabric care benefit is directly related to the amount of deposition of the fabric care benefit agent on the fabric, the performance of the water insoluble fabric care benefit agent on the fabric should theoretically increase proportionately by potentially about 100% and preferably by at least about 200%.
  • the ratio of the delivery enhancing agent to the water insoluble fabric care benefit agent should be from about 1 :50 to 1 :1 and preferably from about 1 :20 to 1 :2.
  • the two components of the present invention can be premixed to form a stable composite prior to formulating into a laundry product or prior to adding to the laundry process or applying to a fabric.
  • the two components can also be formulated into laundry products separately with different orders of addition.
  • the two components may also be mixed together so as to form the fabric care composite of the present invention in situ after formulating into the laundry product or adding to the laundry process.
  • delivery enhancing agent refers to any cationic cellulose or combination of cationic celluloses that significantly enhance the deposition of the water insoluble fabric care benefit agent onto the fabric during laundering.
  • the delivery enhancing agent of the present invention has a strong physical binding capability with the water insoluble fabric care benefit agent. It also has a very strong affinity to natural textile fibers, such as cotton fibers.
  • An effective delivery enhancing agent preferably has a strong binding capability with the water insoluble fabric care benefit agents via physical forces such as van der Waals forces or non-covalent chemical bonds such as hydrogen bonding and/or ionic bonding. It preferably has a very strong affinity to natural textile fibers, particularly cotton fibers.
  • the delivery enhancing agent should be water soluble and have a flexible molecular structure so that it can cover the water insoluble fabric care benefit agent particle surface or hold several particles together. Therefore, the delivery enhancing agent is preferably not cross-linked and preferably does not have a network structure as these both tend to lack molecular flexibility.
  • the net charge of the delivery enhancing agent is preferably positive in order to overcome the repulsion between the fabric care benefit agent and the fabric since most fabrics are comprised of textile fibers that have a slightly negative charge in aqueous environments.
  • fibers exhibiting a slightly negative charge in water include but are not limited to cotton, rayon, silk, wool, etc.
  • the delivery enhancing agent is a cationic or amphoteric polymer.
  • the amphoteric polymers of the present invention will also have a net cationic charge, i.e.; the total cationic charges on these polymers will exceed the total anionic charge.
  • the degree of substitution of the cationic charge can be in the range of from about 0.01 (one cationic charge per 100 polymer repeating units) to 1.00 (one cationic charge on every polymer repeating unit) and preferably from about 0.01 to 0.20.
  • the positive charges could be on the backbone of the polymers or the side chains of polymers.
  • cationic celluloses While there are many ways to calculate the charge density of cationic celluloses, the degree of substitution of the cationic charge can be simply calculated by the cationic charges per 100 glucose repeating units.
  • One cationic charge per 100 glucose repeating units equals to 1% charge density of the cationic celluloses.
  • Preferred cationic celluloses for use herein include those which may or may not be hydrophobically-modified, having a molecular weight of from about 50,000 to about 2,000,000, more preferably from about 100,000 to about 1,000,000, and most preferably from about 200,000 to about 800,000. These cationic materials have repeating substituted anhydro glucose units that correspond to the general Structural Formula I as follows:
  • R 1 , R 2 , R 3 are each independently H, CH , C 8 . 24 alkyl (linear or branched),
  • R 7 is CH 3 , CH 2 CH 3 , a phenyl group, a C 8 . 2 alkyl group (linear or branched), or mixture thereof;
  • R and R are each independently CH 3 , CH 2 CH 3 , phenyl, or mixtures thereof: - P4H R is H, m , or mixtures thereof wherein P is a repeat unit of an addition polymer
  • a cationic monomer such as wherein Z' is a water-soluble anion, preferably chlorine ion, bromine ion or mixtures thereof and q is from about 1 to about 10.
  • Water-soluble anions useful herein include C8-C24 alkyl sulfates, C8-C24 alkyl alkoxy sulfates, preferably alkyl ethoxy sulfates, C8-C24 alkyl sulfonates, C8-C16 alkyl benzene sulfonates, xylene sulfonates, toluene sulfonates, cumene sulfonates, fatty alkyl carboxylates, chlorine ions, bromine ions, or mixtures thereof, while chlorine and/or bromine ions are preferred.
  • the charge density of the cationic celluloses herein (as defined by the number of cationic charges per 100 glucose units) is preferably from about 0.5 % to about 60%, more preferably from about 1% to about 20%, and most preferably from about 2% to about 10%.
  • Alkyl substitution on the anhydroglucose rings of the polymer ranges from about 0.01% to 5% per glucose unit, more preferably from about 0.05% to 2% per glucose unit, of the polymeric material.
  • the cationic cellulose may lightly cross-linked with a dialdehyde such as glyoxyl to prevent forming lumps, nodules or other agglomerations when added to water at ambient temperatures.
  • a dialdehyde such as glyoxyl
  • the cationic cellulose ethers of Structural Formula I likewise include those which are commercially available and further include materials which can be prepared by conventional chemical modification of commercially available materials.
  • Commercially available cellulose ethers of the Structural Formula I type include the JR 30M, JR 400, JR 125, LR 400 and LK 400 polymers, all of which are marketed by Dow Chemical. Water Insoluble Fabric Care Benefit Agents
  • water insoluble fabric care benefit agent refers to any silicone derivatives that are water insoluble and can provide fabric care benefits such as fabric softening, color protection, pill/fuzz reduction, anti-abrasion, anti-wrinkle, and the like to garments and fabrics, particularly on cotton garments and fabrics, when an adequate amount of the material is present on the garment/fabric.
  • fabric care benefits such as fabric softening, color protection, pill/fuzz reduction, anti-abrasion, anti-wrinkle, and the like to garments and fabrics, particularly on cotton garments and fabrics, when an adequate amount of the material is present on the garment/fabric.
  • Non- limiting examples of water insoluble fabric care benefit agents include water-insoluble silicone derivatives and mixtures thereof.
  • water insoluble silicone derivatives are any silicone materials which are not soluble in water, but can be prepared as emulsions, latexes, dispersions, suspensions and the like with suitable surfactants before formulation of the laundry products.
  • Any neat silicones that can be directly emulsified or dispersed into laundry products are also covered in the present invention since laundry products typically contain a number of different surfactants that can behave like emulsifiers, dispersing agents, suspension agents, etc. thereby aiding in the emulsification, dispersion, and/or suspension of the water insoluble silicone derivative.
  • these silicone derivatives can provide one or more fabric care benefit to the fabric including anti-wrinkle, color protection, pill/fuzz reduction, anti-abrasion, fabric • softening and the like.
  • the water insoluble silicone derivatives of the present invention include, but are not limited to 1) non-functionalized silicones such as polydimethylsiloxane (PDMS), including linear, grafted and cyclic structures and 2) functionalized silicones or copolymers with one or more different types of functional groups such as amino, alkoxy, alkyl, phenyl, polyether, acrylate, siliconhydride, mercaptoproyl, carboxylic acid, quaternized nitrogen, etc.
  • PDMS polydimethylsiloxane
  • functionalized silicones or copolymers with one or more different types of functional groups such as amino, alkoxy, alkyl, phenyl, polyether, acrylate, siliconhydride, mercaptoproyl, carboxylic acid, quaternized nitrogen, etc.
  • the particle size can be in the range from about 1 nm to 100 microns and preferably from about 10 nm to about 10 microns including microemulsions ( ⁇ 150 nm), standard emulsions (about 200 nm to about 500 nm) and macroemulsions (about 1 micron to about 20 microns).
  • Water soluble silicone derivatives are outside of the scope of the present invention. Non-limiting examples of commercially available water insoluble silicone derivatives include SM2125 commercially available from GE Silicones,and DC8822 and DC 200 Fluid both of which are commercially available from Dow Corning.
  • a non-limiting list of optional components of the present invention includes laundry detergents, fabric conditioners, and other wash, rinse, and dryer added products.
  • the laundry products may comprise from about 0.1 % to about 20% of the water insoluble fabric care benefit agent, preferably from about 0.2% to about 10%.
  • the laundry products may also comprise from about 0.01% to about 5% of the delivery enhancing agent, preferably from about 0.02% to about 2%.
  • Conventional components of fabric conditioners include but are not limited to surfactants and the like.
  • detergent compositions include but are not limited to surfactants, bleaches and bleach activators, enzymes and enzyme stabilizing agents, suds boosters or suds suppressers, anti-tarnish and anticorrosion agents, non-builder alkalinity sources, chelating agents, organic and inorganic fillers, solvents, hydrotropes, optical brighteners, dyes, perfumes, and modified cellulose ether fabric treatment agents.
  • the fabric care benefit agents or delivery enhancing agent of the present invention may be a component of or added to a detergent composition or a fabric conditioner.
  • the detergent composition may be in the form of a granule, liquid, or tablet.
  • Detergent compositions of the present invention may be made in accordance with U.S. Patent Nos. 6,274,540 and 6,306,817 and WIPO Publication Nos. WO 01/16237 published March 8, 2001 and WO 01/16263 published on March 8, 2001.
  • the laundry products of the present invention may comprise from about 1% to 80% by weight of a surfactant.
  • a surfactant Preferably such compositions comprise from about 5% to 50% by weight of surfactant.
  • Detersive surfactants utilized can be of the anionic, nonionic, zwitterionic, ampholytic or cationic type or can comprise compatible mixtures of these types.
  • Detergent surfactants useful herein are described in U.S. Patent 3,664,961, Norris, issued May 23, 1972, U.S. Patent 3,919,678, Laughlin et al., issued December 30, 1975, U.S. Patent 4,222,905, Cockrell, issued September 16, 1980, and in U.S. Patent 4,239,659, Murphy, issued December 16, 1980.
  • Anionic and nonionic surfactants are preferred.
  • Useful anionic surfactants can themselves be of several different types.
  • water-soluble salts of the higher fatty acids i.e., "soaps"
  • Soaps can be made by direct saponification of fats and oils or by the neutralization of free fatty acids.
  • Particularly useful are the sodium and potassium salts of the mixtures of fatty acids derived from coconut oil and tallow, i.e., sodium or potassium tallow and coconut soap.
  • non-soap anionic surfactants which are suitable for use herein include the water-soluble salts, preferably the alkali metal, and ammonium salts, of organic sulfuric reaction products having in their molecular structure an alkyl group containing from about 10 to about 20 carbon atoms and a sulfonic acid or sulfuric acid ester group.
  • alkyl is the alkyl portion of acyl groups.
  • this group of synthetic surfactants are a) the sodium, potassium and ammonium alkyl sulfates, especially those obtained by sulfating the higher alcohols (Cg-Ci 8 carbon atoms) such as those produced by reducing the glycerides of tallow or coconut oil; b) the sodium, potassium and ammonium alkyl polyethoxylate sulfates, particularly those in which the alkyl group contains from 10 to 22, preferably from 12 to 18 carbon atoms, and wherein the polyethoxylate chain contains from 1 to 15, preferably 1 to 6 ethoxylate moieties; and c) the sodium and potassium alkylbenzene sulfonates in which the alkyl group contains from about 9 to about 15 carbon atoms, in straight chain or branched chain configuration, e.g., those of the type described in U.S.
  • Especially valuable are linear straight chain alkylbenzene sulfonates in which the average number of carbon atoms in the alkyl group is from about 11 to 13, abbreviated as Cn_i3 LAS.
  • Preferred nonionic surfactants are those of the formula R (OC2H4) n OH, wherein
  • R is a C10-C16 alkyl group or a Cg-C ⁇ alkyl phenyl group, and n is from 3 to about 80.
  • Particularly preferred are condensation products of C12-C15 alcohols with from about 5 to about 20 moles of ethylene oxide per mole of alcohol, e.g., C12-C13 alcohol condensed with about 6.5 moles of ethylene oxide per mole of alcohol.
  • nonionic surfactants include polyhydroxy fatty acid amides of the formula:
  • R — C — N — Z wherein R is a C9.17 alkyl or alkenyl, R1 is a methyl group and Z is glycidyl derived from a reduced sugar or alkoxylated derivative thereof. Examples are N-methyl N-l- deoxyglucityl cocoamide and N-methyl N-l -deoxyglucityl oleamide. Processes for making polyhydroxy fatty acid amides are known and can be found in Wilson, U.S. Patent 2,965,576 and Schwartz, U.S. Patent 2,703,798, the disclosures of which are incorporated herein by reference.
  • compositions may also comprise from about 0.1% to 80% by weight of a builder.
  • a builder Preferably such compositions in liquid form will comprise from about 1% to 10% by weight of the builder component.
  • compositions in granular form will comprise from about 1% to 50% by weight of the builder component.
  • Detergent builders are well known in the art and can comprise, for example, phosphate salts as well as various organic and inorganic nonphosphorus builders.
  • Water-soluble, nonphosphorus organic builders useful herein include the various alkali metal, ammonium and substituted ammonium polyacetates, carboxylates, polycarboxylates and polyhydroxy sulfonates.
  • polyacetate and polycarboxylate builders are the sodium, potassium, lithium, ammonium and substituted ammonium salts of ethylene diamine tetraacetic acid, nitrilotriacetic acid, oxydisuccinic acid, mellitic acid, benzene polycarboxylic acids, and citric acid.
  • Other suitable polycarboxylates for use herein are the polyacetal carboxylates described in U.S.
  • Particularly preferred polycarboxylate builders are the oxydisuccinates and the ether carboxylate builder compositions comprising a combination of tartrate monosuccinate and tartrate disuccinate described in U.S. Patent 4,663,071, Bush et al, issued May 5, 1987, the disclosure of which is incorporated herein by reference.
  • nonphosphorus, inorganic builders include the silicates, aluminosilicates, borates and carbonates. Particularly prefe ⁇ ed are sodium and potassium carbonate, bicarbonate, sesquicarbonate, tetraborate decahydrate, and silicates having a weight ratio of Si ⁇ 2 to alkali metal oxide of from about 0.5 to about 4.0, preferably from about 1.0 to about 2.4. Also preferred are aluminosilicates including zeolites. Such materials and their use as detergent builders are more fully discussed in Corkill et al, U. S. Patent No. 4,605,509, the disclosure of which is incorporated herein by reference. Also, crystalline layered silicates such as those discussed in Corkill et al, U. S. Patent No. 4,605,509, incorporated herein by reference, are suitable for use in the detergent compositions of this invention. III. Prefe ⁇ ed Enzymes
  • the laundry products of the present invention may also comprise an enzyme that is a amylase, lipase, selected protease enzyme, or mixtures thereof. Enzymes are normally incorporated into detergent compositions at levels sufficient to provide a "cleaning-effective amount".
  • cleaning-effective amount refers to any amount capable of producing a cleaning, stain removal, soil removal, whitening, deodorizing, or freshness improving effect on substrates such as fabrics.
  • the laundry product compositions of the present invention may contain up to about 5 mg by weight, more typically from about 0.01 mg to about 3 mg, of active enzyme per gram of the detergent composition.
  • compositions herein will typically comprise from about 0.001% to about 5%, preferably from about 0.01% to about 1% by weight of the composition, of a commercial enzyme preparation.
  • Protease enzymes are preferably present in such commercial preparations at levels sufficient to provide from 0.005 to 0.1 Anson units (AU) of activity per gram of composition. Higher active levels may be desirable in highly concentrated detergent formulations.
  • Selected proteases which are useful herein include the subtilisins which are obtained from particular strains of B. subtilis and B. licheniformis.
  • a preferred protease is obtained from a strain of Bacillus, having maximum activity throughout the pH range of 8-12, developed and sold as ESPERASE® by Novo Industries A S of Denmark, hereinafter "Novo".
  • ESPERASE® ESPERASE® by Novo Industries A S of Denmark, hereinafter "Novo”.
  • the preparation of this enzyme and analogous enzymes is described in GB 1,243,784 to Novo.
  • Other suitable proteases include ALCALASE® and SAVINASE® from Novo and MAXATASE® from International Bio-Synthetics, Inc., The Netherlands.
  • a protease having decreased adsorption and increased hydrolysis may be included in the compositions herein, as described in WO 9507791 to Procter & Gamble.
  • Another recombinant trypsin-like protease for detergents suitable herein is described in WO 9425583 to Novo.
  • amylase Any known amylase may be included in the compositions of the present invention.
  • Suitable lipase enzymes for use herein include those produced by microorganisms of the Pseudomonas group, such as Pseudomonas stutzeri ATCC 19.154, as disclosed in GB 1,372,034. See also lipases in Japanese Patent Application 53,20487, laid open Feb. 24, 1978. This lipase is available from Amano Pharmaceutical Co. Ltd., Nagoya, Japan, under the trade name Lipase P "Amano," or "Amano-P.”
  • Other suitable commercial lipases include Amano-CES, lipases ex Chromobacter viscosum, e.g. Chromobacter viscosum var. lipolyticum JNRRLB 3673 from Toyo Jozo Co., Tagata, Japan; Chromobacter viscosum lipases from U.S. Biochemical Corp., U.S.A. and Disoynth Co.,
  • LIPOLASE® enzyme derived from Humicola lanuginosa and commercially available from Novo, see also EP 341,947, is a prefe ⁇ ed lipase for use herein.
  • compositions of the present invention contain a compatible enzyme
  • the compositions preferably also contain an effective enzyme stabilizing system.
  • the enzyme-containing compositions herein may therefore optionally also comprise from about 0.001% to about 10%, preferably from about 0.005% to about 8%, most preferably from about 0.01% to about 6%, by weight of an enzyme stabilizing system.
  • the enzyme stabilizing system can be any stabilizing system which is compatible with the enzymes useful herein. Such a system may be inherently provided by other formulation actives, or be added separately, e.g., by the formulator or by a manufacturer of enzymes.
  • Such stabilizing systems can, for example, comprise calcium ion, boric acid, propylene glycol, short chain carboxylic acids, boronic acids, or mixtures thereof, and are designed to address different stabilization problems depending on the type and physical form of the detergent composition.
  • the laundry product compositions herein are formulated as liquid laundry detergents.
  • the liquid laundry detergent compositions preferably comprise from about 3% to about 98%, preferably from about 15% to about 95%, by weight of the liquid detergent composition, of an aqueous liquid carrier which is preferably water.
  • the liquid laundry compositions according to the present invention should provide a wash solution pH from about 6 to about 10, more preferably from about 7 to about 9, in order to maintain a prefe ⁇ ed stain removal performance by the liquid laundry products according to the present invention.
  • the cleaning compositions may contain alkalinizing agents, pH control agents and/or buffering agents.
  • the density of the laundry detergent compositions herein preferably ranges from about 400 to about 1200 g/litre, more preferably from about 500 to about 1100 g/litre of composition measured at 20°C.
  • laundry product formulations may be made by traditional methods and means as known to one of ordinary skill in the art.

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  • Chemical & Material Sciences (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Organic Chemistry (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Oil, Petroleum & Natural Gas (AREA)
  • Wood Science & Technology (AREA)
  • Engineering & Computer Science (AREA)
  • Health & Medical Sciences (AREA)
  • Molecular Biology (AREA)
  • Emergency Medicine (AREA)
  • Detergent Compositions (AREA)
  • Treatments For Attaching Organic Compounds To Fibrous Goods (AREA)
  • Chemical Or Physical Treatment Of Fibers (AREA)
  • Absorbent Articles And Supports Therefor (AREA)
  • Cosmetics (AREA)

Abstract

Cette invention concerne des compositions pour lessives renfermant un mélange stable d'au moins un agent de soin pour tissus insoluble dans l'eau et d'au moins un agent libérateur qui est de préférence un dérivé de silicium. Ces compositions détergentes pour lessive renferment d'environ 1 % à environ 80 %, en poids de la composition, d'un tensioactif détersif qui est un tensioactif anionique, un tensioactif cationique, un tensioactif non ionique, un tensioactif amphotère, un tensioactif zwitterionique, ou un mélange des tensioactifs précités; d'environ 0,1 % à environ 10 %, en poids de la composition, d'un agent de soin pour tissus insoluble dans l'eau, d'environ 0,01 % à environ 5 %, en poids de la composition, d'un agent libérateur. Dans ces compositions, le rapport entre l'agent libérateur et l'agent de soin pour tissus est compris entre 1:50 et 1:1, environ.
PCT/US2003/028421 2002-09-09 2003-09-09 Utilisation de celluloses cationiques favorisant l'administration d'agents de soin pour tissus WO2004022686A1 (fr)

Priority Applications (7)

Application Number Priority Date Filing Date Title
CA002495117A CA2495117A1 (fr) 2002-09-09 2003-09-09 Utilisation de celluloses cationiques favorisant l'administration d'agents de soin pour tissus
EP03752219A EP1537197B1 (fr) 2002-09-09 2003-09-09 Utilisation de celluloses cationiques favorisant l'administration d'agents de soin pour tissus
BR0314147-0A BR0314147A (pt) 2002-09-09 2003-09-09 Composição de produto para lavanderia
AU2003270521A AU2003270521A1 (en) 2002-09-09 2003-09-09 Using cationic celluloses to enhance delivery of fabric care benefit agents
MXPA05002611A MXPA05002611A (es) 2002-09-09 2003-09-09 Uso de celulosas cationicas para mejorar el suministro de agentes beneficos para el cuidado de las telas.
JP2004534811A JP4145874B2 (ja) 2002-09-09 2003-09-09 布地ケア有益剤の送達を向上させるための陽イオン性セルロース類の使用
DE60319845T DE60319845T2 (de) 2002-09-09 2003-09-09 Verwendung von kationischen cellulosen zur erhöhung der freisetzung von textilpflegemitteln

Applications Claiming Priority (4)

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US40909102P 2002-09-09 2002-09-09
US60/409,091 2002-09-09
US10/375,792 US6897190B2 (en) 2002-02-28 2003-02-26 Detergent compositions including dispersible polyolefin wax and method for using same
US10/375,792 2003-02-26

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WO2004022686A1 true WO2004022686A1 (fr) 2004-03-18

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PCT/US2003/028346 WO2004022685A1 (fr) 2002-09-09 2003-09-09 Utilisation de celluloses cationiques pour ameliorer la liberation d'agents traitants d'entretien de textiles
PCT/US2003/028421 WO2004022686A1 (fr) 2002-09-09 2003-09-09 Utilisation de celluloses cationiques favorisant l'administration d'agents de soin pour tissus

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EP (3) EP2210933A1 (fr)
JP (2) JP4145874B2 (fr)
CN (2) CN1678723A (fr)
AT (2) ATE389708T1 (fr)
AU (2) AU2003270521A1 (fr)
BR (2) BR0314074A (fr)
CA (2) CA2495117A1 (fr)
DE (2) DE60320655T2 (fr)
ES (2) ES2302939T3 (fr)
MX (2) MXPA05002610A (fr)
WO (2) WO2004022685A1 (fr)

Cited By (8)

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WO2004113484A1 (fr) * 2003-06-16 2004-12-29 The Procter & Gamble Company Composition de detergent pour lessive liquide contenant des aides au depot cationique compatible au bore
WO2007120547A1 (fr) * 2006-04-13 2007-10-25 The Procter & Gamble Company Détergents liquides à lessive contenant un polymère cellulosique cationique hydroxyéthyle
WO2008120176A1 (fr) * 2007-04-02 2008-10-09 The Procter & Gamble Company Composition pour le soin des tissus
US7576048B2 (en) 2007-04-04 2009-08-18 The Procter & Gamble Company Liquid laundry detergents containing cationic hydroxyethyl cellulose polymer
WO2011134947A1 (fr) * 2010-04-29 2011-11-03 Henkel Ag & Co. Kgaa Complexes de polyélectrolytes comme substances actives éliminant la saleté
JP2019035074A (ja) * 2017-08-11 2019-03-07 ザ プロクター アンド ギャンブル カンパニー カチオン性多糖ポリマーとアニオン性非石鹸界面活性剤との組み合わせの使用
EP2922936B1 (fr) 2012-11-20 2019-08-14 Unilever PLC, a company registered in England and Wales under company no. 41424 of Compositions de lavage
RU2798937C1 (ru) * 2022-02-02 2023-06-29 Общество С Ограниченной Ответственностью "Объединение "Специальный Текстиль" Состав синтетического моющего средства с антибактериальным эффектом

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GB0514147D0 (en) * 2005-07-11 2005-08-17 Unilever Plc Laundry treatment compositions
JP5364252B2 (ja) * 2007-08-02 2013-12-11 ライオン株式会社 粒状洗剤組成物
ES2394066T3 (es) * 2010-06-24 2013-01-16 The Procter & Gamble Company Composiciones estables que comprenden polímero de celulosa catiónica y celulasa
EP2399978B2 (fr) * 2010-06-24 2020-11-25 The Procter and Gamble Company Compositions liquides stables non aqueuses comprenant un polymère cationique sous forme particulaire

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WO2000059463A1 (fr) * 1999-04-05 2000-10-12 Unilever Plc Compositions liquides contenant un agent benefique pour la peau

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US5476660A (en) * 1994-08-03 1995-12-19 Lever Brothers Company, Division Of Conopco, Inc. Deposition of materials to surfaces using zwitterionic carrier particles
HUP0002572A3 (en) 1997-07-21 2001-04-28 Procter & Gamble Detergent compositions containing mixtures of crystallinity-disrupted surfactants
PH11998001775B1 (en) 1997-07-21 2004-02-11 Procter & Gamble Improved alkyl aryl sulfonate surfactants
DE19926863A1 (de) * 1999-06-12 2000-12-14 Henkel Kgaa Verwendung von partiell oxidiertem Polyethylen als Bügelhilfe in flüssigen wäßrigen Weichspülern
WO2001016263A2 (fr) 1999-08-27 2001-03-08 The Procter & Gamble Company Disponibilite controlee de composants de formulation, compositions et procede de blanchissage utilisant ces produits
DE19941132A1 (de) 1999-08-30 2001-03-01 Basf Ag Verfahren zur kontinuierlichen Herstellung von Glutaraldehyd

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Publication number Priority date Publication date Assignee Title
US3580853A (en) * 1967-09-27 1971-05-25 Procter & Gamble Detergent compositions containing particle deposition enhancing agents
US4237016A (en) * 1977-11-21 1980-12-02 The Procter & Gamble Company Textile conditioning compositions with low content of cationic materials
WO1994003152A2 (fr) * 1992-08-07 1994-02-17 Unilever Plc Composition de detergent
WO2000059463A1 (fr) * 1999-04-05 2000-10-12 Unilever Plc Compositions liquides contenant un agent benefique pour la peau

Cited By (10)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
WO2004113484A1 (fr) * 2003-06-16 2004-12-29 The Procter & Gamble Company Composition de detergent pour lessive liquide contenant des aides au depot cationique compatible au bore
US7226900B2 (en) 2003-06-16 2007-06-05 The Proctor & Gamble Company Liquid laundry detergent composition containing boron-compatible cationic deposition aids
WO2007120547A1 (fr) * 2006-04-13 2007-10-25 The Procter & Gamble Company Détergents liquides à lessive contenant un polymère cellulosique cationique hydroxyéthyle
WO2008120176A1 (fr) * 2007-04-02 2008-10-09 The Procter & Gamble Company Composition pour le soin des tissus
JP2010523833A (ja) * 2007-04-02 2010-07-15 ザ プロクター アンド ギャンブル カンパニー 布地ケア組成物
US7576048B2 (en) 2007-04-04 2009-08-18 The Procter & Gamble Company Liquid laundry detergents containing cationic hydroxyethyl cellulose polymer
WO2011134947A1 (fr) * 2010-04-29 2011-11-03 Henkel Ag & Co. Kgaa Complexes de polyélectrolytes comme substances actives éliminant la saleté
EP2922936B1 (fr) 2012-11-20 2019-08-14 Unilever PLC, a company registered in England and Wales under company no. 41424 of Compositions de lavage
JP2019035074A (ja) * 2017-08-11 2019-03-07 ザ プロクター アンド ギャンブル カンパニー カチオン性多糖ポリマーとアニオン性非石鹸界面活性剤との組み合わせの使用
RU2798937C1 (ru) * 2022-02-02 2023-06-29 Общество С Ограниченной Ответственностью "Объединение "Специальный Текстиль" Состав синтетического моющего средства с антибактериальным эффектом

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BR0314147A (pt) 2005-07-12
CA2495323A1 (fr) 2004-03-18
CA2495117A1 (fr) 2004-03-18
CN1678724A (zh) 2005-10-05
MXPA05002610A (es) 2005-05-05
AU2003270497A1 (en) 2004-03-29
CN1678723A (zh) 2005-10-05
JP2005536618A (ja) 2005-12-02
JP4283224B2 (ja) 2009-06-24
EP2210933A1 (fr) 2010-07-28
EP1537197A1 (fr) 2005-06-08
AU2003270521A1 (en) 2004-03-29
DE60320655D1 (de) 2008-06-12
DE60319845D1 (de) 2008-04-30
EP1537196B1 (fr) 2008-04-30
ES2302939T3 (es) 2008-08-01
DE60319845T2 (de) 2009-03-05
EP1537197B1 (fr) 2008-03-19
BR0314074A (pt) 2005-07-05
DE60320655T2 (de) 2009-06-04
ATE389708T1 (de) 2008-04-15
JP4145874B2 (ja) 2008-09-03
ES2305492T3 (es) 2008-11-01
WO2004022685A1 (fr) 2004-03-18
MXPA05002611A (es) 2005-05-05
ATE393812T1 (de) 2008-05-15
JP2005537408A (ja) 2005-12-08
EP1537196A1 (fr) 2005-06-08

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