EP2046935A2 - Composition de microcapsules stabilisees a base de polymere cationique - Google Patents
Composition de microcapsules stabilisees a base de polymere cationiqueInfo
- Publication number
- EP2046935A2 EP2046935A2 EP07798887A EP07798887A EP2046935A2 EP 2046935 A2 EP2046935 A2 EP 2046935A2 EP 07798887 A EP07798887 A EP 07798887A EP 07798887 A EP07798887 A EP 07798887A EP 2046935 A2 EP2046935 A2 EP 2046935A2
- Authority
- EP
- European Patent Office
- Prior art keywords
- composition
- shell
- cross
- polymer
- microcapsule
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Withdrawn
Links
Classifications
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- 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
- C11D17/0039—Coated compositions or coated components in the compositions, (micro)capsules
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- 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
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- 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
- C11D3/3769—(Co)polymerised monomers containing nitrogen, e.g. carbonamides, nitriles or amines
- C11D3/3773—(Co)polymerised monomers containing nitrogen, e.g. carbonamides, nitriles or amines in liquid compositions
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- 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
- C11D3/50—Perfumes
- C11D3/502—Protected perfumes
- C11D3/505—Protected perfumes encapsulated or adsorbed on a carrier, e.g. zeolite or clay
Definitions
- Consumer products such as fabric care products, personal care products and home care products are well known in the art and usually comprise one or more perfumes to impart the consumer product and/or a substrate treated or applied with the consumer product with a fragrance; however, these perfumes dissipate over time from the consumer product or substrate.
- Another problem with perfumes in consumer products is that they are released prior to an optimal delivery time, and the user of the consumer product is deprived of experiencing the perfume's fragrance.
- a perfume it is desirable for a perfume to be present on clothes treated with a detergent and/or fabric softener long after such treatment, and there is a tendency for perfumes to evaporate or diffuse from the clothes over time.
- Clog P The calculated log P (Clog P) of many perfumes is known in the art, and has been reported, for example, in the Ponoma92 database, available from Daylight Chemical Information Systems, Inc. (Daylight CIS) Irvine. CA. Methods of calculating Clog P are also known in the art. Perfumes with lower Clog P values may be more volatile and exhibit higher aqueous solubility than perfumes having higher Clog P values, and are therefore preferred to be used in consumer products. However when lower Clog P materials are encapsulated, they may have a greater tendency to leach out of, or diffuse out of the shell into the consumer product (preventing optimal delivery of fragrances), and the perfumes may eventually diffuse out of the consumer product prior to use by the consumer.
- fragrance microcapsules are incorporated in consumer products containing solvents and/or surfactants, e.g., shampoos
- stability problems may arise.
- the encapsulated perfume may leach out of the shell.
- the shell may also absorb a solvent, surfactant, or any other material in the consumer product, causing the shell's integrity to be compromised.
- the shell may swell because additional materials diffuse into the shell or the core, or the shell may shrink as materials of the core diffuse out of the shell. Indeed, components of the shell may even diffuse into the consumer product.
- compositions suitable for use in compositions that provide for stability of microcapsules encapsulating fragrance or antimicrobial materials are provided.
- the invention provides a composition
- a microcapsule comprising a shell encapsulating a material having an average Clog P of at least about 2.5 and more than 60% by weight of the material has a Clog P of at least 3.3
- a cross-linked cationic polymer derived from the polymerization of about 5 to 100 mole percent of a cationic vinyl addition monomer, 0 to about 95 mole percent acrylamide. and about 5 to about 500 ppm of a difunctional vinyl addition monomer cross-linking agent.
- the invention provides a method of improving the stability of a product that comprises at least one microcapsule comprising admixing with the product (before, after, or simultaneously with the addition of the at least one microcapsule) a cross-linked cationic polymer derived from the polymerization of about 5 to 100 mole percent of a cationic vinyl addition monomer, 0 to about 95 percent acrylamide, and about 5 to about 500 ppm of a difunctional vinyl addition monomer cross-linking agent, wherein the microcapsule comprises a shell encapsulating a material having an average ClogP of at least 2.5 and more than 60% by weight of the material has a Clog P of at least 3.3.
- ranges are used as a shorthand for describing each and every value that is within the range. Any value within the range can be selected as the terminus of the range. Percentages given below are percent of total weight unless otherwise indicated.
- the present invention is related to the benefit that is provided by use of a cationic polymer in a composition containing microcapsules, in particular to microcapsules having an average Clog P of at least about 2.5 with more than 60% by weight of the material having a Clog P of at least 3.3.
- the addition of the cationic polymer to the composition increases the stability of the microcapsule in the composition compared to compositions lacking such cationic polymer.
- Perfumes are known in the art and may include odoriferous materials which are able to provide a fragrance to consumer products and/or impart a fragrance to a substrate, e.g.. shampoos and conditioners treat hair, laundry detergents and rinse cycle fabric softeners treat fabrics and clothes, glass cleaners treat glass and hard surfaces, colognes, soaps, deodorants, antiperspirants and shower gels treat skin and hair. Perfumes may also counteract malodors and/or provide a fragrance.
- the perfumes may be in liquid state at ambient temperature, although solid perfumes may also be useful.
- Perfumes may include aldehydes, ketones, esters and other chemicals and compounds known in the art, including natural, synthetic perfumes, and mixtures thereof.
- Perfumes useful for the present invention may have relatively simple compositions or may comprise complex mixtures of natural and synthetic chemical components, all of which are intended to provide an odor or fragrance in consumer products, and/or to the substrate. It is understood in the present application that a perfume may be substituted with flavors known in the art, and that the term perfume, as used herein, also includes flavors. Generally, perfumes may be present in consumer products between 0.00001 - 10%.
- Formulations of the invention may comprise unencapsulated fragrance materials in addition to any fragrance material present in the microcapsules.
- Fragrance microcapsules are generally known in the art, see ,e.g., WO/2004016234. US 2005/0153135. US 2005/0256027, US2004/0072719A1, US2004/0072720A1 , US20040071742A1 , US2004/0071746A1 , US 6,194,375, WO 02/074430A1; US 6.620.777, the contents of each patent publication are incorporated herein by reference.
- a fragrance microcapsule generally has a shell which encapsulates a perfume, and optionally other materials, such as solvents, surfactants, hydrophobic polymers, and other materials known in the art.
- the shell may be considered to be made up of a tight collection of strands of polymer(s) and may have a diameter less than 1000 ⁇ m, and the shells may have a mean diameter in the range 1 to 500 ⁇ m, preferably 1 to 300 ⁇ m, more preferably 1 to 50 ⁇ m and most preferably 1 to 10 ⁇ m.
- the size of the shell may be modified by methods known in the art. Preferred sizes for the shell will depend upon their intended use.
- the shell generally prevents leaching of the perfumes from the consumer product.
- the shell may also bind to substrates, and release the perfume under predetermined conditions, i.e., while fabric is being ironed, a fragrance microcapsule on the fabric bursts due to change in temperature, or while fabric is being worn, a fragrance microcapsule bursts due to friction, shearing, or other physical/mechanical stress caused by the movement of the wearer.
- a microcapsule's shell may be made by any of the methods known in the art.
- the shell may be a polymer or resin known in the art. Shells comprised of polyurethane, polyamide, polyolefin, polysaccaharide, protein, silicone, lipid, modified cellulose, gums, polyacrylate, polyphosphate, polystyrene, and polyesters or combinations thereof may be suitable for use in the present invention.
- Preferred shells may be an aminoplast which is formed by the reaction of one of more amines known in the art with one or more aldehydes known in the art, such as formaldehyde.
- aminoplasts may be prepared by polycondensation.
- a preferred aminoplast may be a melamine-formaldehyde or urea-formaldehyde condensate, such as melamine resin or urea-formaldehyde resin.
- Aminoplasts preferably a melamine resin, may be used singularly or in combination with other suitable amides known in the art. crosslinking agents known in the art (e.g.. toluene diisocyanate, divinyl benzene, butane diol diacrylate), and secondary polymers known in the art. such as polymers and co-polymers of maleic anhydride.
- Aminoplasts may also be mixed resins of urea-formalehyde, maleic anhydride copolymers, and melamine-formalehyde.
- the microcapsules of the present invention have a shell, the shell having an inner surface, and an outer surface.
- the inner surface and/or outer surface of the shell may be coated, e.g., with a polymer.
- the coaling on the inner surface and/or outer surface may improve the barrier properties of the shell and thus may enhance retention of the encapsulated materials in surfactant- containing and/or solvent containing consumer products.
- a cationically charged water-soluble polymer known in the art can be coated on shell.
- the water-soluble polymer can also be an amphoteric polymer with a ratio of cationic and anionic functionalities resulting in a net total charge of zero and positive.
- Methods for coating the cationically charged polymer onto the microcapsule are also known in the art.
- the application of a coating to the inner surface of the shell capsules may be carried out by a number of methods known in the art.
- One approach known in the art involves the use of a suitable material for the coating which is insoluble in the material to be encapsulated, but can be dissolved in a water soluble solvent e.g., ethanol, carbitol, which is miscible with the material to be encapsulated.
- the coating material typically a polymer, is dissolved in the solvent and then the solution is dissolved in the material to be encapsulated.
- the material to be encapsulated is then emulsified into a standard aminoplast capsule forming aqueous solution.
- the solvent is lost to the water and the polymer precipitates out from solution at the surface of the emulsion droplets, forming a film at the interface of water/material to be encapsulated.
- An encapsulation process known in the art may then be carried out and the coating may be deposited on the inner surface of the shell.
- a coating material e.g., silicone
- a coating material used may be immiscible with materials to be encapsulated and immiscible with water, and is capable of forming a thin film at the water interface.
- a shell encapsulate comprising a coating of silicone on the inner surface of the shell can be prepared by dispersing the material to be encapsulated within the silicone and then emulsifying this mixture so that an emulsion is formed where droplets of encapsulated material are surrounded by a thin film of silicone. The encapsulation process is then carried out as known in the art.
- a thin film may be formed at the surface by dispersing the material to be encapsulated in water, adding the second material e.g., silicone and allowing it to coat the encapsulating material droplets subsequently.
- An inner surface coating may also be made from a film-forming polymer known in the art, for example: poly(ethylene-maleic anhydride), povidones, waxes e.g. carbowax.
- polyvinylpyrrolidone (PVP) and its co-polymers such as polyvinylpyrrolidone-ethyl acrylate (PVP-EA). polyvinylpyrrolidone-vinyl acrylate.
- polyvinylpyrrolidone methylacrylate PVP-MA
- polyvinylpyrrolidone/vinyl acetate polyvinyl acetal
- polyvinyl butyral polysiloxane
- poly(propylene maleic anhydride) maleic anhydride derivatives and co-polymers of the above, e.g. polyvinyl methyl ether/maleic anhydride.
- the inner wall coating comprises polysiloxane, PVP or PVP co-polymers, more preferably PVP or PVP co- polymers, and even more preferably PVP co-polymers, particularly PVP-MA or PVP-EA.
- a coating may be applied to the outer surface of a shell techniques known in the art, such as by including spraying, fluid bed coating, or precipitating.
- a coating e.g., of a polymer
- a coating may be precipitated from aqueous solution to condense onto the outer surface of the shell or microcapsule, e.g., in the form of a capsules slurry, with precipitation being caused by change of temperature, pH. addition of salt, and other variables and conditions known in the art.
- the shell capsule to be coated is thus formed in a separate first step, prior to the application of the coating to the outer surface of the shell wall.
- a coated shell capsule may be prepared for example, by coacervation or polycondensation.
- the outer surface coating may comprise high molecular weight, film- forming polymers known in the art. which may optionally be cross-linked. "High molecular weight” is meant a molecular weight average of greater than 2000 Da. preferably greater than 4000 Da, more preferably greater than 5000 Da.
- the polymer maybe water-soluble or water- insoluble, preferably water-soluble.
- Suitable polymers for use may include, polyvinyl alcohol (PVOH), styrene-butadiene latex, gelatin, gum arabic, carboxymethyl cellulose, carboxymethyl hydroxyethyl cellulose, hydroxyethyl cellulose, other modified celluloses, sodium alginate, chitosan, casein, pectin, modified starch, polyvinyl acetal. polyvinyl butyral, polyvinyl methyl ether/maleic anhydride. PVP and its co-polymers (e.g. polyvinylpyrro Ii done/vinyl acetate (PVP/VA).
- polyvinyl pyrrolidone/dimethylaminoethyl methacrylate) PVP/DMAEMA
- poly(vinyl pyrrolidone/methacrylamidopropyl trimethyl ammonium chloride) melamine- formaldehyde and urea-formaldehyde.
- the outer surface of the shell is coated with PVOH, PVP or a PVP co-polymer.
- a preferred coated shell may be an aminoplast capsule having a coating of PVOH, PVP or a co-polymer PVP (preferably PVP/DMAEMA) on the outer surface of the shell and/or a coating of a film- forming polymer (preferably PVP-EP) on the inner surface.
- the coating may be cross-linked in any known manner, e.g., by interfacial cross-linking.
- a shell capsule useful herein may have more than one coating on the outer surface of the shell.
- Coated shell capsules typically have a wall thickness in the range of about 0.01 to about 30 ⁇ m, preferably about 0.01 to about 5 ⁇ m. more preferably about 0.03 to about 1 ⁇ m, most preferably about 0.03 to about 0.5 ⁇ m.
- the wall thickness may be regulated and controlled according to the encapsulate size and by varying the relative proportions of coating and shell polymer.
- the weight ratio of coating to shell wall is typically in the range of about 0.01 to about 10: 1 , preferably about 0.1 : 1 to about 10: 1 , more preferably about 0.1 : 1 to about 3:1.
- the weight ratio of polymer shell wall material to encapsulated material is in the range of about 1: 10 to about 3:2 and preferably in the range of about 1:10 to about 1:2.
- the coating on the inner surface and/or outer surface will increase these weight ratios.
- materials having an average Clog P value equal to or greater than 2.5 may be encapsulated, preferably within the range of about 3 to about 5.
- Materials used in uncoated microcapsules may include materials wherein at least about 60% have a Clog P equal to or greater than about 3.3, preferably greater than about 4.
- average Clog P is meant the average Clog P for all of the encapsulated materials.
- the average Clog P of the encapsulated materials may be raised, for example, by adding a solvent having a high ClogP, e.g., about 6 or greater, wherein the solvent is miscible with the other encapsulated materials.
- One or more perfumes may be used in the present invention as a mixture of perfumes.
- a mixture of perfumes greater than about 60 weight percent of the fragrance materials have a Clog P of greater than about 3.3.
- more than about 80 weight percent of the fragrances have a Clog P value of greater than about 4.0, and more preferably, more than about 90 weight percent of the fragrances have a Clog P value of greater than about 4.5 may be used.
- the microcapsule contains a core within the shell, and the core comprises a perfume or other benefit agent, such as a flavorant or antibacterial material, and may optionally contain other materials known in the art, for example, hydrophobic solvents such as triglyceride oil, mono and diglycerides, mineral oil, silicone oil. diethyl phthalate, polyalphaolefins, fatty alcohols, castor oil and isopropyl myristate.
- suitable solvents include those having reasonable affinity for the perfume, and the solvent may have a Clog P greater than 3.3, preferably greater than 6 and most preferably greater that 10.
- a preferred solvent may be isopropyl myristate.
- a preferred solvent may also be silicone, such polydimethylsiloxane and polydimethylcyclosiloxane.
- a preferred solvent may be diethyl phthalate.
- the solvent may be greater than about 30 weight percent, preferably greater than about 50 weight percent and more preferably greater than about 70 weight percent of the core.
- hydrophobic polymers in a microcapsule may also improve stability of the microcapsule by slowing diffusion of the perfume from the shell.
- the amount of the hydrophobic polymer may be less than 80% of the microcapsule by weight, preferably less than 50%, and most preferably less than 20%.
- a hydrophobic polymer may be ethyl cellulose, hydroxypropyl cellulose, cellulose acetate butyrate. ethylene vinyl acetate, polystyrene, and PVP and ester terminated polyamides or amide terminated polyamides.
- a cationic polymer is added to the consumer product to increase the stability of the microcapsule.
- the cationic polymer in the present invention is a cross-linked polymer which is cross-linked using a cross-linking agent of a difunctional vinyl addition monomer at a level of about 5-500 ppm. preferably about 70 to about 300 ppm, preferably about 75 to about 200ppm, and most preferably of from about 80 to about 150 ppm.
- the cationic polymer may be a cationic vinyl polymer.
- a cationic vinyl polymer may be derived from the polymerization of from about 5 to 100 mole percent of a cationic vinyl addition monomer and 0 to about 95 mole percent of acrylamide.
- the difunctional vinyl addition monomer may be a polyethylene glycol diacrylic ester having a weight average molecular weight of from 300 to 3,000.
- the cationic polymer may be derived from the polymerization of about 5 to 100 mole percent of a cationic vinyl addition monomer, 0 to about 95 mole percent of acrylamide, and about 70 to about 300 ppm of a difunctional vinyl addition monomer crosslinking agent.
- the difunctional vinyl addition monomer may be a polyethylene glycol diacrylic ester having a weight average molecular weight of about 300 to about 3,000.
- the cationic polymer may also be a cross-linked cationic vinyl addition polymer derived from the polymerization of about 15 to about 70 mole percent of a quaternary ammonium salt of dimethyl/aminoethylmethacrylate and about 30 to about 85 mole percent of acrylamide, and about 0.005 to about 0.025 weight percent of the polyethylene glycol diacrylic ester.
- the polyethylene glycol diacrylic ester may be polyethylene glycol dimethacrylate.
- the cationic polymer may be prepared as water in oil emulsions, wherein the cross-linked polymers are dispersed in the oil, preferably a mineral oil.
- a cationic polymer may be a cross-linked copolymer of a quaternary ammonium acrylate or methacrylate in combination with an acrylamide comonomer. Additional description of cationic polymers useful in the present invention may be found in U.S. Patent Nos. 4,806,345 and 6,864,223, which are incorporated herein by reference.
- a composition may comprise about 0.001 % to about 40% total weight of the cationic polymer, preferably about 0.01% to about 10%, more preferably, about 0.01% to about 5%.
- the amount of cationic polymer present will depend upon the composition and the microcapsule used therein.
- the cationic polymer may be admixed to the consumer product before, during or after the addition of a microcapsule to the consumer product.
- the cationic polymer is well suited for use in a variety of well-known consumer products comprising a microcapsule, such as oral care products, toothpastes, mouthwashes, personal care products, lotions, creams, shampoos, conditioners, hair gel, antiperspirants, deodorants, shaving creams, hair spray, colognes, body wash, home care products, laundry detergent, fabric softeners, liquid dish detergents, tumble dryer sheets, automatic dish washing detergents, and hard surface cleaners.
- These consumer products may employ surfactant, solvents and emulsifying systems that are well known in the art.
- a fragrance is used to provide the consumer with a pleasurable fragrance during and after using the product or to mask unpleasant odors from some of the functional ingredients used in the product.
- a problem with the use of encapsulated fragrance in product bases is the loss of the fragrance before the optimal time for fragrance delivery.
- the microcapsule may be in an aqueous solution of a consumer product.
- the microcapsule may be in the continuous phase of an oil-in- water emulsion of a consumer product.
- the microcapsule may be in the discontinuous phase of an oil-in-water emulsion of a consumer product.
- the microcapsule may be in the discontinuous phase of a water-in-oil emulsion of a consumer product.
- the microcapsule may be in the continuous phase of a water-in-oil emulsion of a consumer product.
- Consumer products may be made using an aqueous base containing a surfactant, although some products use glycols, polyhydric alcohols, alcohols, or silicone oils as the dominant solvent or carrier.
- Suitable surfactant agents for use in the present invention include those surfactants that are commonly used in consumer products such as laundry detergents, fabric softeners and the like.
- the products commonly include cationic surfactants which also are used as fabric softeners; as well as nonioinic and anionic surfactants which are known in the art.
- Surfactants are normally present at levels of about 1 to 30 weight %. In some instances the surfactant loading may be more than 85, typically more than 95 and greater than about 99 weight % of the formulated product.
- the present invention is further illustrated for use in a consumer product, such as a fabric softener composition.
- Fabric softener compositions are known in the art, and contain a fabric softening component, and other optional materials such as perfumes, chelators, preservatives, dyes, soil release polymers, and thickeners.
- Other optional ingredients may also include solvents, alcohols, amphoteric and non-ionic surfactants, fatty alcohols, fatty acids, organic or inorganic salts, pH buffers, antifoams, germicides, fungicides, antioxidants, corrosion inhibitors, enzymes, optical brighteners, antifoams, and other materials known in the art.
- a fabric softener composition may be substantially free of anionic surfactants known in the art, such as. lithium dodecyl sulfate, or sodium dodecyl sulfate.
- substantially free is meant that the fabric softener composition contains less than 5% weight of anionic surfactant, preferably less than 1% by weight, more preferably less than .5% by weight and still more preferably less than 0.1 % by weight of an anionic surfactant.
- a fabric softener composition may be substantially free of water soluble builder salts known in the art, such as alkali metal phosphates, such as sodium phosphate and potassium phosphate.
- substantially free is meant that the fabric softener composition contains less than 5% weight of a builder salt, preferably less than 1% by weight, more preferably less than 0.5% by weight and still more preferably less than 0.1% by weight an water soluble builder salt.
- Fabric softening components in fabric softener compositions are well known in the art. and may include cationic surfactants, quaternary ammonium salts (acyclic quaternary ammonium salts, ester quaternary ammonium salts, cyclic quaternary ammonium salts, diamido quaternary ammonium salts, biodegradable quaternary ammonium salt, polymeric ammonium salts), polyquats, tertiary fatty amines, carboxylic acids, esters of polyhydric alcohols, fatty alcohols, ethoxylated fatty alcohols, alkyphenols. ethoxylated alkyphenols, ethoxylated fatty amines, difatty. ethoxylated monolycerides, ethoxylated diglycerides, mineral oils, clays, and polyols.
- quaternary ammonium salts acyclic quaternary ammonium salts, ester quaternary
- a fabric softener composition may comprise about 0.01% to about 35% by weight of one or more fabric softening components.
- the present invention may comprise about 0.5% to about 25% weight of a fabric softening component.
- the present invention may comprise about 1.5% to about 12% of a fabric softening component.
- the present invention may comprise about 15% to about 24% of a fabric softening component.
- the amount of the components in a fabric softener composition will depend on the purpose of the formulation, i.e., whether the formulation concentrated or dilute.
- the fabric softening component may, for example, be about 0.1% to about 50% of the total weight of the composition, e.g.. about 10% to about 25% for a concentrated composition and about 1 to about 10% for a dilute composition.
- the fabric softener composition may also have one or more chelators, dyes, fatty alcohols, preservatives and/or perfumes, and/or other ingredients as known in the art.
- a fabric softening component may be an esterquat (or mixture of esterquats) having the formula of structure 1
- R ⁇ represents -(CH 2 )
- R 2 and R 3 represent -(CH 2 ) s -R 5 where R 5 represents an acyloxy group containing from 8 to 22 carbon atoms, benzyl, phenyl. (Cl -C4)-alkyl substituted phenyl, OH or H;
- R 4 represents an aliphatic hydrocarbon group having from 8 to 22 carbon atoms; q, s, and t, each independently, represent an integer from 1 to 3; and
- X " is a softener compatible anion.
- a particular softener for use in the present invention is produced by reacting two moles of fatty acid methyl ester with one mole of triethanolamine followed by quaternization with dimethyl sulfate (further details on this preparation method are disclosed in US 3,915.867, which is incorporated herein by reference). The reaction products are distributed as follows: (a) 50% diesterquat material; (b) 20% monoesterquat; and (c) 30% triesterquat.
- esterquat compounds described herein are prepared by quaternizing the product of the condensation reaction between a fatty acid fraction containing at least one saturated or unsaturated linear or branched fatty acid, or derivative, and at least one functional ized tertiary amine, wherein the molar ratio of the fatty acid fraction to tertiary amine is about 1.7 : 1.
- the method of manufacture for such a esterquat surfactant is described in US Patent 5,637,743 (Stepan), the disclosure of which is incorporated herein by reference.
- the aforementioned molar ratio will determine the equilibrium between the mono, di and tri-esterquat compounds in the products. For example, using a molar ratio of about 1.7 results in a normalized distribution of about 34% mono-esterquat, about 56% of di-esterquat and about 10% of tri-esterquat which is a fatty ester quat compound in accordance with the invention. On the other hand, for example, using a molar ratio of about 1.96 results in a normalized distribution of about 21% mono-esterquat, 61% of di-esterquat and 18% of tri- esterquat.
- a preferred fabric softening component may thus include a quaternized fatty acid triethanolamine ester salt, e.g., a triethanolamine-esterquat tallow.
- a preferred fabric softening component of the present invention may include a di-alkyl ester of triethanol ammonium methyl sulfate, or a dihydrogenated tallowoylethyl hydroxyethylmonium methosulfate.
- Fabric softening components may be purchased from Kao Corporation under the product name Tetranyl L 1/90 or Tetranyl ATl-75.
- Fabric softener compositions may also comprise soil release polymers (SRP's).
- SRP's are well known in the art, and may include polymers which are absorbed onto fabric fibers where they counteract resoiling of the fibers.
- the polymers may include polyesters and copolymers of terephthalic acid, polyesters of and co-polymers of ethylene glycol, copolymers of ethylene glycol and benzene, and polyethylene terephthalate.
- the polymers may include nonionic polyesters.
- the polymers may be modified whereby a portion of the ethylene glycol is removed and replaced with a high molecular weight hydroxy-terminated polyethylene glycol.
- Chelating agents are well known in the art. and may be present at a level of at least about 0.001%, by weight, of the fabric softening composition, preferably about 0.001% to about 1%, more preferably about 0.01% to about 0.5%, more preferably about 0.06% - 0.1% by weight.
- the chelating agents may be selected from among amino carboxylic acid compounds and organo aminophosphonic acid compounds, and mixtures of the same.
- Suitable amino carboxylic acid compounds may include: ethylenediamine tetraacetic acid, N- hydroxyethylenediamine triacetic acid, nitrilotriacetic acid, and diethylenelriamine pentaacetic acid.
- Suitable organo aminophosphonic acid compounds may include methylenephosphonic acid, 1-hydroxyethane 1.1-diphosphonic acid, and aminotrimethylene phosphonic acid.
- a preferred chelating agent may be an aminotrimethylene phosphonic acid, which may be obtained from Solutia, Inc. (St. Louis, Missouri, USA) as Dequest 2000.
- Preservatives are well known in the art, and may include lactic acid, formaldehyde, or other preservatives known in the art.
- a fabric softener composition may comprise 0% to about 10% weight of a preservative, preferably, about 0.01 % to about 2%, more preferably about 0.05% to about 0.5%.
- a preferred preservative in the present invention may be lactic acid.
- Fatty alcohols and aliphatic alcohols are known in the art.
- Fatty alcohols may have carbon chain which are fully saturated or unsaturated.
- Preferred fatty alcohols include Cm- C 28 alcohols, preferably Ci 6 - is- Ci 3 -Ci 5 alcohols, and mixtures thereof.
- a fabric softener composition may comprise 0% to about 10% weight of a fatty alcohol, preferably about 0.1% to about 5%. and more preferably about 0.1% to about 0.5% of a fatty alcohol.
- Dyes are well known in the art and may comprise 0% to about 5% of a product.
- the invention provides a method of delivering a fragTance or antimcrobial material in a product comprising admixing any of compositions into a consumer product.
- the consumer product may be a oral care product, toothpaste, mouthwash, personal care product, lotion, cream, shampoo, conditioner, hair gel. antiperspirant, deodorant, antiperspirant and deodorant, shaving cream, hair spray, cologne, body wash, home care product, laundry detergent, fabric softener, liquid dish detergent, tumble dryer sheet, automatic dish detergent, or hard surface cleaner.
- compositions are prepared by mixing in deionized water to create an emulsion (percentages are percentage of total weight):
- compositions are prepared by mixing in deionized water to create an emulsion (percentages are percentage of total weight):
- Cotton terry towels are washed in laundry washing machines with equal amounts of compositions FC#3 and FC#4. Following washing, the towels are stored for 1 week at temperature for 1 week. 3 months at 35°C. and one month at 43°C. Following storage. a panel of 20 judges is asked to rate the intensity of the perfume on the towel, and the intensity of the perfume on the towel after rubbing the towel several times. The results are shown in the chart below. The towels washed in FC#4 with the encapsulated fragrance with the cationic polymer outperformed the towels washed in FC#3 without the encapsulated fragrance.
Abstract
La présente invention concerne l'utilisation d'un polymère cationique permettant une stabilité des microcapsules dans une composition, dans laquelle la microcapsule comprend un matériau d'encapsulation d'enveloppe ayant un ClogP moyen d'au moins 2,5 et plus de 60 % en poids des substances encapsulées ont un ClogP d'au moins 3,3. Le polymère cationique est dérivé de la polymérisation d'environ 5 à 100 moles pour cent d'un monomère d'addition vinylique cationique, de 0 à environ 95 pour cent d'acrylamide, et d'environ 5 à environ 500 ppm d'un agent de réticulation monomère d'addition vinylique bifonctionnel. Le polymère cationique et la substance encapsulée peuvent être utilisés, par exemple, dans une composition d'assouplissant.
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US47967906A | 2006-06-30 | 2006-06-30 | |
PCT/US2007/071782 WO2008005693A2 (fr) | 2006-06-30 | 2007-06-21 | composition de microcapsules stabilisées à base de polymère cationique |
Publications (1)
Publication Number | Publication Date |
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EP2046935A2 true EP2046935A2 (fr) | 2009-04-15 |
Family
ID=38658485
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
EP07798887A Withdrawn EP2046935A2 (fr) | 2006-06-30 | 2007-06-21 | Composition de microcapsules stabilisees a base de polymere cationique |
Country Status (11)
Country | Link |
---|---|
EP (1) | EP2046935A2 (fr) |
CN (1) | CN101506344A (fr) |
AU (1) | AU2007269428A1 (fr) |
BR (1) | BRPI0713074A2 (fr) |
CA (1) | CA2656326A1 (fr) |
IL (1) | IL196157A0 (fr) |
MX (1) | MX2008016479A (fr) |
NO (1) | NO20090477L (fr) |
RU (1) | RU2009102970A (fr) |
WO (1) | WO2008005693A2 (fr) |
ZA (1) | ZA200900074B (fr) |
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2007
- 2007-06-21 MX MX2008016479A patent/MX2008016479A/es unknown
- 2007-06-21 BR BRPI0713074-0A patent/BRPI0713074A2/pt not_active IP Right Cessation
- 2007-06-21 EP EP07798887A patent/EP2046935A2/fr not_active Withdrawn
- 2007-06-21 CN CNA2007800317503A patent/CN101506344A/zh active Pending
- 2007-06-21 RU RU2009102970/04A patent/RU2009102970A/ru not_active Application Discontinuation
- 2007-06-21 AU AU2007269428A patent/AU2007269428A1/en not_active Abandoned
- 2007-06-21 CA CA002656326A patent/CA2656326A1/fr not_active Abandoned
- 2007-06-21 WO PCT/US2007/071782 patent/WO2008005693A2/fr active Application Filing
-
2008
- 2008-12-24 IL IL196157A patent/IL196157A0/en unknown
-
2009
- 2009-01-05 ZA ZA200900074A patent/ZA200900074B/xx unknown
- 2009-01-29 NO NO20090477A patent/NO20090477L/no not_active Application Discontinuation
Non-Patent Citations (1)
Title |
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See references of WO2008005693A3 * |
Also Published As
Publication number | Publication date |
---|---|
CN101506344A (zh) | 2009-08-12 |
IL196157A0 (en) | 2009-09-22 |
CA2656326A1 (fr) | 2008-01-10 |
WO2008005693A3 (fr) | 2008-02-21 |
ZA200900074B (en) | 2010-03-31 |
NO20090477L (no) | 2009-01-29 |
AU2007269428A1 (en) | 2008-01-10 |
BRPI0713074A2 (pt) | 2012-07-17 |
WO2008005693A2 (fr) | 2008-01-10 |
RU2009102970A (ru) | 2010-08-10 |
MX2008016479A (es) | 2009-01-22 |
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