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USRE37555E1 - Process and composition for multicomponent one hundred percent solid fabric softeners - Google Patents

Process and composition for multicomponent one hundred percent solid fabric softeners Download PDF

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Publication number
USRE37555E1
USRE37555E1 US09/330,621 US33062199A USRE37555E US RE37555 E1 USRE37555 E1 US RE37555E1 US 33062199 A US33062199 A US 33062199A US RE37555 E USRE37555 E US RE37555E
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Prior art keywords
fatty acid
quaternary ammonium
tertiary amine
ammonium compound
carbon atoms
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US09/330,621
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Jeannene A. Ackerman
Michael Miller
David E. Whittlinger
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GODSCHMIDT SKW OLEOCHEMICALS LLC
Evonik Goldschmidt Corp
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Goldschmidt Chemical Corp
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Assigned to GOLDSCHMIDT CHEMICAL CORPORATION reassignment GOLDSCHMIDT CHEMICAL CORPORATION ASSIGNMENT OF ASSIGNORS INTEREST (SEE DOCUMENT FOR DETAILS). Assignors: GOLDSCHMIDT SKW OLEOCHEMICALS LLC
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    • CCHEMISTRY; METALLURGY
    • C11ANIMAL OR VEGETABLE OILS, FATS, FATTY SUBSTANCES OR WAXES; FATTY ACIDS THEREFROM; DETERGENTS; CANDLES
    • C11DDETERGENT COMPOSITIONS; USE OF SINGLE SUBSTANCES AS DETERGENTS; SOAP OR SOAP-MAKING; RESIN SOAPS; RECOVERY OF GLYCEROL
    • C11D17/00Detergent materials or soaps characterised by their shape or physical properties
    • C11D17/04Detergent materials or soaps characterised by their shape or physical properties combined with or containing other objects
    • C11D17/041Compositions releasably affixed on a substrate or incorporated into a dispensing means
    • C11D17/042Water soluble or water disintegrable containers or substrates containing cleaning compositions or additives for cleaning compositions
    • C11D17/044Solid compositions
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K8/00Cosmetics or similar toiletry preparations
    • A61K8/18Cosmetics or similar toiletry preparations characterised by the composition
    • A61K8/30Cosmetics or similar toiletry preparations characterised by the composition containing organic compounds
    • A61K8/33Cosmetics or similar toiletry preparations characterised by the composition containing organic compounds containing oxygen
    • A61K8/36Carboxylic acids; Salts or anhydrides thereof
    • A61K8/361Carboxylic acids having more than seven carbon atoms in an unbroken chain; Salts or anhydrides thereof
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K8/00Cosmetics or similar toiletry preparations
    • A61K8/18Cosmetics or similar toiletry preparations characterised by the composition
    • A61K8/30Cosmetics or similar toiletry preparations characterised by the composition containing organic compounds
    • A61K8/33Cosmetics or similar toiletry preparations characterised by the composition containing organic compounds containing oxygen
    • A61K8/37Esters of carboxylic acids
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K8/00Cosmetics or similar toiletry preparations
    • A61K8/18Cosmetics or similar toiletry preparations characterised by the composition
    • A61K8/30Cosmetics or similar toiletry preparations characterised by the composition containing organic compounds
    • A61K8/40Cosmetics or similar toiletry preparations characterised by the composition containing organic compounds containing nitrogen
    • A61K8/41Amines
    • A61K8/416Quaternary ammonium compounds
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61QSPECIFIC USE OF COSMETICS OR SIMILAR TOILETRY PREPARATIONS
    • A61Q5/00Preparations for care of the hair
    • A61Q5/12Preparations containing hair conditioners
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07CACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C211/00Compounds containing amino groups bound to a carbon skeleton
    • C07C211/62Quaternary ammonium compounds
    • C07C211/63Quaternary ammonium compounds having quaternised nitrogen atoms bound to acyclic carbon atoms
    • CCHEMISTRY; METALLURGY
    • C11ANIMAL OR VEGETABLE OILS, FATS, FATTY SUBSTANCES OR WAXES; FATTY ACIDS THEREFROM; DETERGENTS; CANDLES
    • C11DDETERGENT COMPOSITIONS; USE OF SINGLE SUBSTANCES AS DETERGENTS; SOAP OR SOAP-MAKING; RESIN SOAPS; RECOVERY OF GLYCEROL
    • C11D1/00Detergent compositions based essentially on surface-active compounds; Use of these compounds as a detergent
    • C11D1/86Mixtures of anionic, cationic, and non-ionic compounds
    • CCHEMISTRY; METALLURGY
    • C11ANIMAL OR VEGETABLE OILS, FATS, FATTY SUBSTANCES OR WAXES; FATTY ACIDS THEREFROM; DETERGENTS; CANDLES
    • C11DDETERGENT COMPOSITIONS; USE OF SINGLE SUBSTANCES AS DETERGENTS; SOAP OR SOAP-MAKING; RESIN SOAPS; RECOVERY OF GLYCEROL
    • C11D11/00Special methods for preparing compositions containing mixtures of detergents
    • CCHEMISTRY; METALLURGY
    • C11ANIMAL OR VEGETABLE OILS, FATS, FATTY SUBSTANCES OR WAXES; FATTY ACIDS THEREFROM; DETERGENTS; CANDLES
    • C11DDETERGENT COMPOSITIONS; USE OF SINGLE SUBSTANCES AS DETERGENTS; SOAP OR SOAP-MAKING; RESIN SOAPS; RECOVERY OF GLYCEROL
    • C11D17/00Detergent materials or soaps characterised by their shape or physical properties
    • C11D17/04Detergent materials or soaps characterised by their shape or physical properties combined with or containing other objects
    • C11D17/041Compositions releasably affixed on a substrate or incorporated into a dispensing means
    • CCHEMISTRY; METALLURGY
    • C11ANIMAL OR VEGETABLE OILS, FATS, FATTY SUBSTANCES OR WAXES; FATTY ACIDS THEREFROM; DETERGENTS; CANDLES
    • C11DDETERGENT COMPOSITIONS; USE OF SINGLE SUBSTANCES AS DETERGENTS; SOAP OR SOAP-MAKING; RESIN SOAPS; RECOVERY OF GLYCEROL
    • C11D17/00Detergent materials or soaps characterised by their shape or physical properties
    • C11D17/04Detergent materials or soaps characterised by their shape or physical properties combined with or containing other objects
    • C11D17/041Compositions releasably affixed on a substrate or incorporated into a dispensing means
    • C11D17/046Insoluble free body dispenser
    • CCHEMISTRY; METALLURGY
    • C11ANIMAL OR VEGETABLE OILS, FATS, FATTY SUBSTANCES OR WAXES; FATTY ACIDS THEREFROM; DETERGENTS; CANDLES
    • C11DDETERGENT COMPOSITIONS; USE OF SINGLE SUBSTANCES AS DETERGENTS; SOAP OR SOAP-MAKING; RESIN SOAPS; RECOVERY OF GLYCEROL
    • C11D17/00Detergent materials or soaps characterised by their shape or physical properties
    • C11D17/04Detergent materials or soaps characterised by their shape or physical properties combined with or containing other objects
    • C11D17/041Compositions releasably affixed on a substrate or incorporated into a dispensing means
    • C11D17/047Arrangements specially adapted for dry cleaning or laundry dryer related applications
    • CCHEMISTRY; METALLURGY
    • C11ANIMAL OR VEGETABLE OILS, FATS, FATTY SUBSTANCES OR WAXES; FATTY ACIDS THEREFROM; DETERGENTS; CANDLES
    • C11DDETERGENT COMPOSITIONS; USE OF SINGLE SUBSTANCES AS DETERGENTS; SOAP OR SOAP-MAKING; RESIN SOAPS; RECOVERY OF GLYCEROL
    • C11D3/00Other compounding ingredients of detergent compositions covered in group C11D1/00
    • C11D3/0005Other compounding ingredients characterised by their effect
    • C11D3/001Softening compositions
    • CCHEMISTRY; METALLURGY
    • C11ANIMAL OR VEGETABLE OILS, FATS, FATTY SUBSTANCES OR WAXES; FATTY ACIDS THEREFROM; DETERGENTS; CANDLES
    • C11DDETERGENT COMPOSITIONS; USE OF SINGLE SUBSTANCES AS DETERGENTS; SOAP OR SOAP-MAKING; RESIN SOAPS; RECOVERY OF GLYCEROL
    • C11D1/00Detergent compositions based essentially on surface-active compounds; Use of these compounds as a detergent
    • C11D1/02Anionic compounds
    • C11D1/04Carboxylic acids or salts thereof
    • CCHEMISTRY; METALLURGY
    • C11ANIMAL OR VEGETABLE OILS, FATS, FATTY SUBSTANCES OR WAXES; FATTY ACIDS THEREFROM; DETERGENTS; CANDLES
    • C11DDETERGENT COMPOSITIONS; USE OF SINGLE SUBSTANCES AS DETERGENTS; SOAP OR SOAP-MAKING; RESIN SOAPS; RECOVERY OF GLYCEROL
    • C11D1/00Detergent compositions based essentially on surface-active compounds; Use of these compounds as a detergent
    • C11D1/38Cationic compounds
    • C11D1/40Monoamines or polyamines; Salts thereof
    • CCHEMISTRY; METALLURGY
    • C11ANIMAL OR VEGETABLE OILS, FATS, FATTY SUBSTANCES OR WAXES; FATTY ACIDS THEREFROM; DETERGENTS; CANDLES
    • C11DDETERGENT COMPOSITIONS; USE OF SINGLE SUBSTANCES AS DETERGENTS; SOAP OR SOAP-MAKING; RESIN SOAPS; RECOVERY OF GLYCEROL
    • C11D1/00Detergent compositions based essentially on surface-active compounds; Use of these compounds as a detergent
    • C11D1/38Cationic compounds
    • C11D1/42Amino alcohols or amino ethers
    • CCHEMISTRY; METALLURGY
    • C11ANIMAL OR VEGETABLE OILS, FATS, FATTY SUBSTANCES OR WAXES; FATTY ACIDS THEREFROM; DETERGENTS; CANDLES
    • C11DDETERGENT COMPOSITIONS; USE OF SINGLE SUBSTANCES AS DETERGENTS; SOAP OR SOAP-MAKING; RESIN SOAPS; RECOVERY OF GLYCEROL
    • C11D1/00Detergent compositions based essentially on surface-active compounds; Use of these compounds as a detergent
    • C11D1/38Cationic compounds
    • C11D1/52Carboxylic amides, alkylolamides or imides or their condensation products with alkylene oxides
    • C11D1/528Carboxylic amides (R1-CO-NR2R3), where at least one of the chains R1, R2 or R3 is interrupted by a functional group, e.g. a -NH-, -NR-, -CO-, or -CON- group
    • CCHEMISTRY; METALLURGY
    • C11ANIMAL OR VEGETABLE OILS, FATS, FATTY SUBSTANCES OR WAXES; FATTY ACIDS THEREFROM; DETERGENTS; CANDLES
    • C11DDETERGENT COMPOSITIONS; USE OF SINGLE SUBSTANCES AS DETERGENTS; SOAP OR SOAP-MAKING; RESIN SOAPS; RECOVERY OF GLYCEROL
    • C11D1/00Detergent compositions based essentially on surface-active compounds; Use of these compounds as a detergent
    • C11D1/38Cationic compounds
    • C11D1/58Heterocyclic compounds
    • CCHEMISTRY; METALLURGY
    • C11ANIMAL OR VEGETABLE OILS, FATS, FATTY SUBSTANCES OR WAXES; FATTY ACIDS THEREFROM; DETERGENTS; CANDLES
    • C11DDETERGENT COMPOSITIONS; USE OF SINGLE SUBSTANCES AS DETERGENTS; SOAP OR SOAP-MAKING; RESIN SOAPS; RECOVERY OF GLYCEROL
    • C11D1/00Detergent compositions based essentially on surface-active compounds; Use of these compounds as a detergent
    • C11D1/38Cationic compounds
    • C11D1/62Quaternary ammonium compounds
    • CCHEMISTRY; METALLURGY
    • C11ANIMAL OR VEGETABLE OILS, FATS, FATTY SUBSTANCES OR WAXES; FATTY ACIDS THEREFROM; DETERGENTS; CANDLES
    • C11DDETERGENT COMPOSITIONS; USE OF SINGLE SUBSTANCES AS DETERGENTS; SOAP OR SOAP-MAKING; RESIN SOAPS; RECOVERY OF GLYCEROL
    • C11D1/00Detergent compositions based essentially on surface-active compounds; Use of these compounds as a detergent
    • C11D1/66Non-ionic compounds
    • C11D1/667Neutral esters, e.g. sorbitan esters

Definitions

  • the invention relates to a method of producing a mixture of a quaternary ammonium compound, fatty acid, fatty acid ester and tertiary amine salt in situ which is a highly functional mixture that is manufactured in a single step reaction whereby quaternization is completed without the aid of solvents, especially flammable solvents.
  • the single step reaction process eliminates separate blending of individual components.
  • quaternary ammonium compounds are usually conducted in stainless steel or glass-lined equipment to which a tertiary amine is charged and a solvent.
  • Flammable solvents such as isopropyl alcohol are generally used although mixtures of isopropyl alcohol and water sometimes are employed or water alone is used. Flammable solvents are also undesirable because they are a fire hazard and special handling procedures are required when they are used. In many applications, these solvents have to be stripped from the mixture when the reaction is completed because the ultimate use of the product is in a solventless or solid form.
  • the reactants are loaded into the reactor they are heated to a temperature of about 50 to about 100° C. after which a quaternizing reagent is added.
  • a quaternizing reagent is added.
  • an exotherm is produced as a result of the quaternizing reaction and the reactor and its contents have to be cooled.
  • the rate of addition of the quaternizing agent can also be controlled in order to minimize or eliminate the exotherm.
  • the solvent, if any is employed in the quaternizing reaction is stripped from the quaternary ammonium compound obtained since some commercial uses for the compounds are in solventless systems. Additionally, bulk shipments of quaternary ammonium compounds with solvents adds to transportion costs which is another reason to remove the solvents.
  • quaternary ammonium compounds The largest use for quaternary ammonium compounds is as a fabric softener and presently accounts for more than about three quarters of the total market for these material. Some fabric softeners are supplied as a liquid dispersion of from about 3% to about 10% by weight of the quaternary ammonium compound which is adapted to be added during the rinse cycle of a commercial or home laundering operation. Another significant fabric softening application is the utilization of quaternary ammonium compounds in combination with a substrate such as a nonwoven fabric or a polymeric foam such as a polyurethane foam, this substrate so treated being added to a fabric dryer such as a clothes dryer while the fabric or clothes are still damp.
  • the quaternary ammonium compound is formulated usually with a fatty acid ester which promotes the transfer of the quaternary ammonium compound from the nonwoven or porous polymeric substrate to the fabric or clothes.
  • quaternary ammonium compounds are now being added to both solid and liquid laundry detergent compositions so that the quaternary ammonium compound can be incorporated as a fabric softener during the wash cycle of fabrics or clothes.
  • the most successfully utilized quaternary ammonium compounds in this last respect are the dimethyl (dihydrogenated tallow) ammonium chlorides or methyl sulfates.
  • Other quaternary ammonium compounds such as imidazolines and amidoamine quaternaries are also used in this regard.
  • the quaternary ammonium compound is used on a substrate for transfer to fabric or clothing in a fabric or clothes dryer, it has generally been the practice to separately blend the fatty acid ester into the quaternary ammonium compound which involves the extra manufacturing steps of transportion, handling and blending of the fatty acid esters into the quaternary ammonium compounds. If these steps can be eliminated a cost savings could be realized.
  • Quaternary ammonium compounds are also used to manufacture organomodified clays which may be added to drilling muds utilized in drilling oil wells, the organomodified clay providing improved lubrication and rheological properties of the drilling muds.
  • organoclays are also employed as thixotropic agents in plastisols, organosols, paints and other protective coatings, grease additives, foundry additives, cosmetics, resins and printing inks.
  • the most common quaternary ammonium compounds employed in this regard are methyldi(hydrogenated tallow) benzylammonium chloride, dimethyldi(hydrogenated tallow) ammonium chloride and dimethyl(hydrogenated tallow) benzylammonium chloride.
  • Quaternary ammonium compounds are also employed as bactericides the most common of which is the quaternary ammonium compound of benzylchloride and a dimethylalkylamine, the alkyl group having from about 12 to about 16 carbon atoms as well as trimethyl alkyl ammonium chlorides where the alkyl group is a long chain alkyl such as an octadecyl group. Additionally, dimethyldicoconut-oil fatty ammonium chlorides are also effective disinfectants e.g.
  • bactericides or bacteristats especially against anaerobic bacteria which are sulfate reducers that are found in oil wells, these bacteria causing severe corrosion problems and plugging of formations which this type of quaternary ammonium compound can minimize or eliminate. Additionally, these quaternary ammonium compounds effective against anaerobic bacteria are also effective in removing oil from sand stone formations in oil wells and provide a two-fold effect or functioning not only as a bactericide but also in promoting so-called secondary recovery of oil.
  • quaternary compounds are trimethylalkylammonium chloride, pentaethoxystearylammonium chloride, dimethylstearylbenzylammonium chloride and dimethyldialkylammonium chlorides.
  • the advantage of the method of the present invention is that it provides a composition that is non-flammable and it is ready to be flaked or powdered because of its bulk form and can be used as a fabric softener, a fabric lubricant, a hair condition as well as an anti-static agent that can be released from a substrate such as a nonwoven fabric or a polymeric foam.
  • These mixtures can also be used in combination with synthetic detergents or as lubricant, an emulsifier, in cosmetic preparations hair conditioning components clay modifiers, bactericidal compositions and as a floculant.
  • the invention relates to a method for producing a quaternary ammonium mixture that is highly functional by means of a single step reaction as well as the various compositions that can be obtained thereby and therewith.
  • the invention is directed to a method of producing a mixture of a quaternary ammonium compound, fatty acid, fatty acid ester and tertiary amine salt by reacting a tertiary amine, quaternizing agent and fatty acid, each in amount so that said mixture will contain at least a quaternary ammonium compound, a fatty acid, fatty acid ester and a tertiary amine salt.
  • the tertiary amine employed according to the invention has the formula:
  • R, R 1 and R 2 can be any of the following in any combination.
  • R 4 is lower alkylene and R 3 is any of R, R 1 or R 2 ;
  • said tertiary amine is an imidazoline of the formula:
  • R 5 is a linear or branched chain, aliphatic saturated or unsaturated hydrocarbon group having up to about 22 carbon atoms and R 6 is a lower alkylene group;
  • said quaternizing agent being known in the art and which will produce a quaternary ammonium compound having an anion A ⁇ .
  • these quaternizing agents are those having the formula R 7 (a ⁇ b) X ;
  • R 7 is a lower alkyl group or cyclo lower alkyl group such as benzyl, cyclohexylmethyl, tolyl, xylyl, naphthylmethyl
  • X may be a chlorine, iodine, bromine, sulfate, methyl sulfate, carbonate, phosphate, borate group, formate, acetate, propionate, adipate, benzoate and the like where (a) is equal to the valence of X and (b) is from 1 to the valence of X.
  • said fatty acid is a linear or branched chain aliphatic saturated or unsaturated fatty acid having from about 12 to about 22 carbon atoms based on coconut oil, vegetable oils, seed oils animal fats and fish oils;
  • tertiary amines that can be employed in this regard include dimethylamino propyl amine, amino ethylanolamine, distearly methyl amine, dihydrogenated tallow methyl amine, ditallow methyl amine, dimethyl hydrogenated tallow amine, dimethyl coco amine, distearyl ethoxyethyl amine, stearyl bis-hydroxyethyl amine, stearyl bis (polyethoxy ethanol) amine, bis (tallowamidoethyl) 2-hydroxyethyl amine, bis (tallowamidoethyl) 2-hydroxylpropyl amine, 1-hydrogenated tallow amido ethyl -2-hydrogenated tallow imidazoline 1-ethylene bis (2tallow, 1-methyl, imidazolinium) dimethyl amino propyl tallow amidoamine and hydrogenated tallow hydroxyethyl imidazoline
  • R 9 , R 10 , R 11 and R 12 are subsequently defined.
  • Imidazoline compounds that may be used are also described in Demangeon (supra), whereas the quarternizing agents include;
  • the quaternary ammonium compound thus obtained has the formula:
  • R, R 1 , R 2 , R 3 , R 4 , R 5 , R 6 and R 7 have been defined above;
  • a ⁇ is an anion based on R 7 (a ⁇ b) X or equivalent anions known in the quaternary ammonium compound art;
  • R 9 is about C8 to C30, preferably about C12 to about C18 alkyl or akenyls alkenyl
  • R 10 and R 11 are independently hydrogen or C1 to about C4 alkyl
  • R 12 is C1 to about C4 alkyl
  • m is about 2 to about 3
  • a ⁇ is preferably an anion such as chloride, bromide, sulfate, methosulfate, nitrite, phosphate and carbosylate (i.e., acetate, adipate, propionate, benzoate)
  • the tertiary amine salt has the formula:
  • R 8 is a linear or a branched chain aliphatic saturated or unsaturated hydrocarbon group having from about 11 to about 21 carbon atoms.
  • lower alkoxy, lower alkylene and lower alkyl are intended to include compounds having up to about 3 or about 4 carbon atoms including the various isomeric configurations thereof e.g. t-butyl, i-butyl, i-propyl and the like and the various mixtures thereof whether such mixtures of such groups contain components having one, or two, or three or four carbon atoms or more and also where such groups individually or in combination are in any of their isomeric forms.
  • the tertiary amine, quaternizing agent and fatty acid are reacted with one another each in an amount so that the mixture obtained contains from about 10 weight percent to about 80 weight percent and especially from about 35 weight percent to about 55 weight percent of said quaternary ammonium compound, about 15 weight percent to about 70 weight percent and especially from about 10 weight percent to about 30 weight percent of said salt, about 1 weight percent to about 70 weight percent and especially from about 5 weight percent to about 25 weight percent of said ester and from about 5 weight percent to about 70 weight percent and especially from about 15 weight percent to about 35 weight percent of said fatty acid wherein the ratio of said quaternary ammonium compound to said salt is from about 2:1 to about 1:2.
  • the method of the invention is preferably practiced so that the quaternary ammonium compound that is obtained has the structural formula (I) wherein at least one of R, R 1 and R 2 is a branched chain or linear aliphatic saturated or unsaturated hydrocarbon group having from about 12 to about 22 carbon atoms, preferably saturated, and especially those based on hard tallow acids (i.e. hydrogenated tallow fatty acids) and the balance, if any of the aforesaid R, R 1 and R 2 groups is a lower alkyl group and R 7 is a lower alkyl group.
  • X is a sulfate group.
  • the invention also relates to a mixture of the various quaternary ammonium compounds as described above in combination with the various fatty acid esters, fatty acids, and tertiary amine salts also as described previously and in the amounts and ratios as described previously.
  • the invention also relates to a fabric softening article of manufacture comprising a fabric softening amount of any of the mixtures as described herein operatively associated with a substrate that will release such mixture to a fabric under fabric softening conditions encountered in a fabric or clothes dryer and includes the use of any of the aforesaid mixtures in a fabric softening relationship with a nonwoven or woven fiber or a polymeric open-celled or substantially open-celled foam substrate, such combination being prepared in a manner well known in the art.
  • the mixture is employed in an amount from about 0.1 to about 10 gms and especially 1 to about 39 grms per 9 in. by 11 in. sheet.
  • the various polymeric foams that are employed in this respect comprise polyurethane foams as well as any of the art known equivalent foams.
  • the invention is directed to a fabric cleaning composition
  • a detergent in combination with a fabric softening amount of any of the mixtures described herein.
  • These detergents can be any of the art known anionic, cationic, nonionic or amphoteric synthetic detergents or wetting agents that are well known in the art or a soap i.e. the reaction product of a fatty acid with a alkaline hydroxide that is water soluble e.g. fatty acid reaction products of sodium, potassium or ammonium hydroxides or amines or the art known equivalents thereof.
  • alkyl alcohol ethoxylates as well as those noted in the prior art cited.herein.
  • the mixture of the invention is incorporated into the detergents (whether solid or liquid) by blending in a manner well known in the art.
  • the amount of the mixture employed is any where from about 1 to about 50 and especially from about 2 to about 30 wt. % based on the quaternary ammonium compound and the active components of the detergent i.e. the component of the detergent that has both organophilic and hydrophilic groups.
  • the amine was charged to a clean, dry reactor which was heated to 140° F. A slight nitrogen purge was employed over the amine that was charged to prevent it from coming into contact with any air that might enter into the reactor during the reaction.
  • the stearic acid was then charged, mixed and heated to 140° F. after which the dimethyl sulfate was charged in increments sufficient to maintain the temperature of the reaction mixture at 140-170° F.
  • the reaction is exothermic and the end point of the reaction is indicated to some degree when an exotherm is no longer obtained.
  • the resultant mixture was allowed to cool.
  • the foregoing method produced a reaction mixture which was analyzed by NMR analysis showing that the mixture obtained had the following components:

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Abstract

The invention relates to a method of producing a mixture of a quaternary ammonium compound, fatty acid, fatty acid ester and tertiary amine salt in situ which is a highly functional mixture that is manufactured in a single step reaction whereby quaternization is completed without the aid of solvents, especially flammable solvents. The single step reaction process eliminates separate blending of individual components. The compositions obtained can be used as fabric softeners, in modified clays, as hair treating compounds and as disinfectants.

Description

This application is a reissue application of U.S. application Ser. No. 793,216, filed Nov. 7, 1991, now U.S. Pat. No. 5,221,794, which in turn is a continuation of application Ser. No. 472,738, filed on Jan. 31, 1990, now abandoned.
BACKGROUND OF THE INVENTION
1. Field of the Invention
The invention relates to a method of producing a mixture of a quaternary ammonium compound, fatty acid, fatty acid ester and tertiary amine salt in situ which is a highly functional mixture that is manufactured in a single step reaction whereby quaternization is completed without the aid of solvents, especially flammable solvents. The single step reaction process eliminates separate blending of individual components.
2. Brief Description of the Prior Art
The preparation of quaternary ammonium compounds is usually conducted in stainless steel or glass-lined equipment to which a tertiary amine is charged and a solvent. Flammable solvents such as isopropyl alcohol are generally used although mixtures of isopropyl alcohol and water sometimes are employed or water alone is used. Flammable solvents are also undesirable because they are a fire hazard and special handling procedures are required when they are used. In many applications, these solvents have to be stripped from the mixture when the reaction is completed because the ultimate use of the product is in a solventless or solid form.
After the reactants are loaded into the reactor they are heated to a temperature of about 50 to about 100° C. after which a quaternizing reagent is added. In some instances an exotherm is produced as a result of the quaternizing reaction and the reactor and its contents have to be cooled. The rate of addition of the quaternizing agent can also be controlled in order to minimize or eliminate the exotherm. As noted previously, in some instances, the solvent, if any is employed in the quaternizing reaction is stripped from the quaternary ammonium compound obtained since some commercial uses for the compounds are in solventless systems. Additionally, bulk shipments of quaternary ammonium compounds with solvents adds to transportion costs which is another reason to remove the solvents.
The largest use for quaternary ammonium compounds is as a fabric softener and presently accounts for more than about three quarters of the total market for these material. Some fabric softeners are supplied as a liquid dispersion of from about 3% to about 10% by weight of the quaternary ammonium compound which is adapted to be added during the rinse cycle of a commercial or home laundering operation. Another significant fabric softening application is the utilization of quaternary ammonium compounds in combination with a substrate such as a nonwoven fabric or a polymeric foam such as a polyurethane foam, this substrate so treated being added to a fabric dryer such as a clothes dryer while the fabric or clothes are still damp. The quaternary ammonium compound is formulated usually with a fatty acid ester which promotes the transfer of the quaternary ammonium compound from the nonwoven or porous polymeric substrate to the fabric or clothes.
Lastly, quaternary ammonium compounds are now being added to both solid and liquid laundry detergent compositions so that the quaternary ammonium compound can be incorporated as a fabric softener during the wash cycle of fabrics or clothes. The most successfully utilized quaternary ammonium compounds in this last respect are the dimethyl (dihydrogenated tallow) ammonium chlorides or methyl sulfates. Other quaternary ammonium compounds such as imidazolines and amidoamine quaternaries are also used in this regard.
Where the quaternary ammonium compound is used on a substrate for transfer to fabric or clothing in a fabric or clothes dryer, it has generally been the practice to separately blend the fatty acid ester into the quaternary ammonium compound which involves the extra manufacturing steps of transportion, handling and blending of the fatty acid esters into the quaternary ammonium compounds. If these steps can be eliminated a cost savings could be realized.
Quaternary ammonium compounds are also used to manufacture organomodified clays which may be added to drilling muds utilized in drilling oil wells, the organomodified clay providing improved lubrication and rheological properties of the drilling muds. These organoclays are also employed as thixotropic agents in plastisols, organosols, paints and other protective coatings, grease additives, foundry additives, cosmetics, resins and printing inks. The most common quaternary ammonium compounds employed in this regard are methyldi(hydrogenated tallow) benzylammonium chloride, dimethyldi(hydrogenated tallow) ammonium chloride and dimethyl(hydrogenated tallow) benzylammonium chloride.
Quaternary ammonium compounds are also employed as bactericides the most common of which is the quaternary ammonium compound of benzylchloride and a dimethylalkylamine, the alkyl group having from about 12 to about 16 carbon atoms as well as trimethyl alkyl ammonium chlorides where the alkyl group is a long chain alkyl such as an octadecyl group. Additionally, dimethyldicoconut-oil fatty ammonium chlorides are also effective disinfectants e.g. bactericides or bacteristats, especially against anaerobic bacteria which are sulfate reducers that are found in oil wells, these bacteria causing severe corrosion problems and plugging of formations which this type of quaternary ammonium compound can minimize or eliminate. Additionally, these quaternary ammonium compounds effective against anaerobic bacteria are also effective in removing oil from sand stone formations in oil wells and provide a two-fold effect or functioning not only as a bactericide but also in promoting so-called secondary recovery of oil.
An additional use of quaternary compounds is in hair treatment because of the antistatic effects obtained with such compounds, as well as the increased wetting which promotes improvements in both wet and dry combing or brushing and improves luster and feel. The most commonly used quaternary ammonium compounds in this respect are trimethylalkylammonium chloride, pentaethoxystearylammonium chloride, dimethylstearylbenzylammonium chloride and dimethyldialkylammonium chlorides.
It is therefore an object to overcome these and other difficulties encountered in the prior art.
It is also an object of the present invention to provide a method for manufacturing a mixture of quaternary ammonium compounds with a fatty ester inter allia which can be used in fabric softening applications. It is also an object of the present invention to provide such mixtures.
It is a further object of the invention to provide mixtures of quaternary ammonium compounds with fatty acid esters, amine salts and fatty acids that can be employed in any or all of the foregoing applications.
These and other objects have been achieved according to the present invention which will be further understood in view of the following description and claims.
SUMMARY OF THE INVENTION
It has been found that a highly functional mixture of a quaternary ammonium compound, a fatty acid ester, an ammonium salt and a fatty acid can be obtained in a single step reaction without the aid of solvents, especially flammable solvents to thereby produce a mixture of highly functional components. The single step reaction thereby eliminates the separate blending of such individual components as the fatty acid ester, the ammonium salt and the fatty acid with the quaternary ammonium compound.
The advantage of the method of the present invention is that it provides a composition that is non-flammable and it is ready to be flaked or powdered because of its bulk form and can be used as a fabric softener, a fabric lubricant, a hair condition as well as an anti-static agent that can be released from a substrate such as a nonwoven fabric or a polymeric foam. These mixtures can also be used in combination with synthetic detergents or as lubricant, an emulsifier, in cosmetic preparations hair conditioning components clay modifiers, bactericidal compositions and as a floculant.
DETAILED DESCRIPTION
As noted, the invention relates to a method for producing a quaternary ammonium mixture that is highly functional by means of a single step reaction as well as the various compositions that can be obtained thereby and therewith.
In its broadest aspect the invention is directed to a method of producing a mixture of a quaternary ammonium compound, fatty acid, fatty acid ester and tertiary amine salt by reacting a tertiary amine, quaternizing agent and fatty acid, each in amount so that said mixture will contain at least a quaternary ammonium compound, a fatty acid, fatty acid ester and a tertiary amine salt. The tertiary amine employed according to the invention has the formula:
Figure USRE037555-20020219-C00001
where R, R1 and R2 can be any of the following in any combination.
(1) linear or branched chain saturated or unsaturated hydrocarbon groups having up to about 22 carbon atoms;
(2) a lower hydroxy alkyl group;
(3) an alkyl amido alkylene group of the formula:
Figure USRE037555-20020219-C00002
where R4 is lower alkylene and R3 is any of R, R1 or R2;
(4) lower alkoxy group;
(5) poly(oxyloweralkylene) group; so that at least one of R, R1 or R2 is one of said linear or branched chain aliphatic saturated or unsaturated hydrocarbon groups;
or said tertiary amine is an imidazoline of the formula:
Figure USRE037555-20020219-C00003
where R5 is a linear or branched chain, aliphatic saturated or unsaturated hydrocarbon group having up to about 22 carbon atoms and R6 is a lower alkylene group;
said quaternizing agent being known in the art and which will produce a quaternary ammonium compound having an anion A. Generally these quaternizing agents are those having the formula R7 (a−b)X;
where R7 is a lower alkyl group or cyclo lower alkyl group such as benzyl, cyclohexylmethyl, tolyl, xylyl, naphthylmethyl, and X may be a chlorine, iodine, bromine, sulfate, methyl sulfate, carbonate, phosphate, borate group, formate, acetate, propionate, adipate, benzoate and the like where (a) is equal to the valence of X and (b) is from 1 to the valence of X.
said fatty acid is a linear or branched chain aliphatic saturated or unsaturated fatty acid having from about 12 to about 22 carbon atoms based on coconut oil, vegetable oils, seed oils animal fats and fish oils;
Various tertiary amines that can be employed in this regard include dimethylamino propyl amine, amino ethylanolamine, distearly methyl amine, dihydrogenated tallow methyl amine, ditallow methyl amine, dimethyl hydrogenated tallow amine, dimethyl coco amine, distearyl ethoxyethyl amine, stearyl bis-hydroxyethyl amine, stearyl bis (polyethoxy ethanol) amine, bis (tallowamidoethyl) 2-hydroxyethyl amine, bis (tallowamidoethyl) 2-hydroxylpropyl amine, 1-hydrogenated tallow amido ethyl -2-hydrogenated tallow imidazoline 1-ethylene bis (2tallow, 1-methyl, imidazolinium) dimethyl amino propyl tallow amidoamine and hydrogenated tallow hydroxyethyl imidazoline
Figure USRE037555-20020219-C00004
where R9, R10, R11 and R12 are subsequently defined.
The prior art also disclosed other amines that may be used such as those described in the U.S. Patents to Marschner, U.S. Pat. No. 4,859,456; Caswell et al., U.S. Pat. No. 4,857,213; Demangeon, U.S. Pat. No. 4,851,141 and Mermelstein et al., U.S. Pat. No. 4,844,824 all of which are incorporated by reference (also referred to hereafter as “the prior art cited herein.”)
Imidazoline compounds that may be used are also described in Demangeon (supra), whereas the quarternizing agents include;
dimethyl sulfate,
diethyl sulfate,
methyl chloride,
methyl bromide and
benzyl chloride as well as those cited in the prior art cited herein.
The quaternary ammonium compound thus obtained has the formula:
Figure USRE037555-20020219-C00005
where R, R1, R2, R3, R4, R5, R6 and R7 have been defined above;
where Ais an anion based on R7 (a−b)X or equivalent anions known in the quaternary ammonium compound art;
Figure USRE037555-20020219-C00006
where R9 is about C8 to C30, preferably about C12 to about C18 alkyl or akenyls alkenyl
R10 and R11 are independently hydrogen or C1 to about C4 alkyl R12 is C1 to about C4 alkyl
m is about 2 to about 3
Ais preferably an anion such as chloride, bromide, sulfate, methosulfate, nitrite, phosphate and carbosylate (i.e., acetate, adipate, propionate, benzoate)
Figure USRE037555-20020219-C00007
where R9, R10, R12, m and Ahave been previously defined.
The tertiary amine salt has the formula:
Figure USRE037555-20020219-C00008
and the fatty acid ester has the formula:
Figure USRE037555-20020219-C00009
wherein R8 is a linear or a branched chain aliphatic saturated or unsaturated hydrocarbon group having from about 11 to about 21 carbon atoms.
As used throughout this specification the terms lower alkoxy, lower alkylene and lower alkyl are intended to include compounds having up to about 3 or about 4 carbon atoms including the various isomeric configurations thereof e.g. t-butyl, i-butyl, i-propyl and the like and the various mixtures thereof whether such mixtures of such groups contain components having one, or two, or three or four carbon atoms or more and also where such groups individually or in combination are in any of their isomeric forms.
In another embodiment, according to the method of the invention the tertiary amine, quaternizing agent and fatty acid are reacted with one another each in an amount so that the mixture obtained contains from about 10 weight percent to about 80 weight percent and especially from about 35 weight percent to about 55 weight percent of said quaternary ammonium compound, about 15 weight percent to about 70 weight percent and especially from about 10 weight percent to about 30 weight percent of said salt, about 1 weight percent to about 70 weight percent and especially from about 5 weight percent to about 25 weight percent of said ester and from about 5 weight percent to about 70 weight percent and especially from about 15 weight percent to about 35 weight percent of said fatty acid wherein the ratio of said quaternary ammonium compound to said salt is from about 2:1 to about 1:2.
In one embodiment, the method of the invention is preferably practiced so that the quaternary ammonium compound that is obtained has the structural formula (I) wherein at least one of R, R1 and R2 is a branched chain or linear aliphatic saturated or unsaturated hydrocarbon group having from about 12 to about 22 carbon atoms, preferably saturated, and especially those based on hard tallow acids (i.e. hydrogenated tallow fatty acids) and the balance, if any of the aforesaid R, R1 and R2 groups is a lower alkyl group and R7 is a lower alkyl group. In another embodiment X is a sulfate group.
The invention also relates to a mixture of the various quaternary ammonium compounds as described above in combination with the various fatty acid esters, fatty acids, and tertiary amine salts also as described previously and in the amounts and ratios as described previously.
The invention also relates to a fabric softening article of manufacture comprising a fabric softening amount of any of the mixtures as described herein operatively associated with a substrate that will release such mixture to a fabric under fabric softening conditions encountered in a fabric or clothes dryer and includes the use of any of the aforesaid mixtures in a fabric softening relationship with a nonwoven or woven fiber or a polymeric open-celled or substantially open-celled foam substrate, such combination being prepared in a manner well known in the art. The mixture is employed in an amount from about 0.1 to about 10 gms and especially 1 to about 39 grms per 9 in. by 11 in. sheet.
The various polymeric foams that are employed in this respect comprise polyurethane foams as well as any of the art known equivalent foams.
Additionally, the invention is directed to a fabric cleaning composition comprising a detergent in combination with a fabric softening amount of any of the mixtures described herein. These detergents can be any of the art known anionic, cationic, nonionic or amphoteric synthetic detergents or wetting agents that are well known in the art or a soap i.e. the reaction product of a fatty acid with a alkaline hydroxide that is water soluble e.g. fatty acid reaction products of sodium, potassium or ammonium hydroxides or amines or the art known equivalents thereof.
These surfactants are further described in Kirk-Othmer, Encyclopedia of Chemical Technology, 3rd Edition Vol. 22 pp. 332-432 which is incorporated herein by reference. Some specific detergents that are especially suitable in this regard include:
Detergents that can be employed in this respect comprise
alkyl benzene sulfate,
sodium lauryl ether sulfate
nonyl phenyl ethoxylates and
alkyl alcohol ethoxylates as well as those noted in the prior art cited.herein.
The mixture of the invention is incorporated into the detergents (whether solid or liquid) by blending in a manner well known in the art. The amount of the mixture employed is any where from about 1 to about 50 and especially from about 2 to about 30 wt. % based on the quaternary ammonium compound and the active components of the detergent i.e. the component of the detergent that has both organophilic and hydrophilic groups.
The following example is illustrative.
The method of the invention as well as a mixture obtained according to this method is examplified by the preparation of a mixture employing the following components in the indicated amounts.
Components M.W. Moles % by Wt.
Dihydrogenated Tallow- 523 1.00 56.63
Methyl-Amine
Stearic Acid 30.00
Dimethyl Sulfate 126 0.98 13.37
The amine was charged to a clean, dry reactor which was heated to 140° F. A slight nitrogen purge was employed over the amine that was charged to prevent it from coming into contact with any air that might enter into the reactor during the reaction. The stearic acid was then charged, mixed and heated to 140° F. after which the dimethyl sulfate was charged in increments sufficient to maintain the temperature of the reaction mixture at 140-170° F. The reaction is exothermic and the end point of the reaction is indicated to some degree when an exotherm is no longer obtained. When the reaction was completed, the resultant mixture was allowed to cool. The foregoing method produced a reaction mixture which was analyzed by NMR analysis showing that the mixture obtained had the following components:
%
Quaternary Ammonium compound 46
Fatty Acid 22
Tertiary Amine and Amine Salt 19
Methyl Ester 13
Although the invention has been described by reference to some embodiments, it is not intended that the novel method or the mixture obtained thereby as well as the fabric softening article of manufacture and the detergent containing a fabric softening amount of the mixture be limited thereby but that certain embodiments are intended being included as falling within the broad scope and spirit of the foregoing disclosure and the following claims.

Claims (17)

We claim:
1. A method of producing a mixture of quaternary ammonium compound, fatty acid, fatty acid ester, and tertiary amine salt by
reacting in a solvent free system, a tertiary amine, quaternizing agent, and fatty acid each in an amount so that said mixture will contain at least a quaternary ammonium compound, fatty acid, fatty acid ester and tertiary amine salt, wherein said tertiary amine has the formula:
Figure USRE037555-20020219-C00010
wherein R, R1 or R2 are:
(1) a linear or branched chain aliphatic saturated or unsaturated hydrocarbon group having up to about 22 carbon atoms;
(2) a hydroxy lower alkyl group;
(3) an alkyl amide alkylene group of the formula;
Figure USRE037555-20020219-C00011
where R4 is lower alkylene and wherein R3 is (1), (2), (4) or (5);
(4) a lower alkoxy group;
(5) a poly(oxyloweralkylene) group; so that at least one of R, R1 and R2 is one of said hydrocarbon groups or one of said hydroxy lower alkyl groups;
or said tertiary amine is an imidazoline of the formula;
Figure USRE037555-20020219-C00012
wherein R5 is a linear or branched chain aliphatic saturated or unsaturated hydrocarbon group having up to about 22 carbon atoms and R6 is a lower alkylene group,
said quaternizing agent being is capable of producing a quaternary ammonium compound having anions A;
said fatty acid is a linear or branched chain saturated or unsaturated fatty acid having from about 12 to about 22 carbon atoms;
said quaternary ammonium compound having has the formula:
Figure USRE037555-20020219-C00013
wherein R7 is a lower alkyl group or cyclo lower alkyl group;
andor the salts of (I) and (II) wherein R— is hydrogen;
said tertiary amine salt has the formula;
Figure USRE037555-20020219-C00014
said fatty acid ester having has the formula:
Figure USRE037555-20020219-C00015
wherein R8 is a linear or branched chain, aliphatic saturated or unsaturated hydrocarbon group having from about 11 to about 21 carbon atoms;
and where said tertiary amine, quaternizing agent and fatty acid are reacted with one another in an amount so that said mixture obtained contains about 10 wt. % to about 80 wt. % of said quaternary ammonium compound, about 15 wt. % to about 70 wt. % of said tertiary amine salt, about 1 wt. % to about 70 wt. % of said ester and about 5 wt. % to about 70 wt. % of said fatty acid whereinand the ratio of said quaternary ammonium compound to said tertiary amine salt is from about 2:1 to about 1:2 on a weight basis.
2. The A method of claim 1 where said producing a mixture of quaternary ammonium compound, fatty acid, fatty acid ester, and tertiary amine salt by reacting in a solvent free system, a tertiary amine, quaternizing agent, and fatty acid each in an amount so that said mixture will contain at least a quaternary ammonium compound, fatty acid, fatty acid ester and tertiary amine salt, wherein
said tertiary amine is an imidazoline having the formula:
Figure USRE037555-20020219-C00016
or is an amine of the formula:
Figure USRE037555-20020219-C00017
where
R9 is alkyl or alkenyl having about 8 to about 30 carbon atoms;
R10 and R 11 are independently hydrogen or alkyl having up to about 4 carbon atoms; and
R12 is alkyl having up to about 4 carbon atoms, said quaternizing agent is capable of producing a quaternary ammonium compound having anions A ;
said fatty acid is a linear or branched chain saturated or unsaturated fatty acid having from about 12 to about 22 carbon atoms;
and said quaternary ammonium compound has the formula:
Figure USRE037555-20020219-C00018
where
R9 is alkyl or akenyls having about 8 to about 30 carbon atoms;
R10 and R11 are independently hydrogen or alkyl having up to about 4 carbon atoms;
R12 is alkyl having up to about 4 carbon atoms; and the salts of (III) or (IV) where R12 on the nitrogen atom is hydrogen
and said tertiary amine salt has the formula:
Figure USRE037555-20020219-C00019
and wherein said tertiary amine, quaternizing agent and fatty acid are reacted with one another in an amount so that said mixture obtained contains about 10 wt. % to about 80 wt. % of said quaternary ammonium compound, about 15 wt. % to about 70 wt. % of said tertiary amine salt, about 1 wt. % to about 70 wt. % of said ester and about 5 wt. % to about 70 wt. % of said fatty acid and the ratio of said quaternary ammonium compound to said tertiary amine salt is from about 2:1 to about 1:2 on a weight basis.
3. The method of any of claims 1 or 2 where said tertiary amine, quaternizing agent and fatty acid are reacted with one another in an amount so that said mixture obtained contains about 35 wt. % to about 55 wt. % of said quaternary ammonium compound, about 10 wt. % to about 30 wt. % of said tertiary amine salt, about 5 wt. % to about 25 wt. % of said ester and about 15 wt. % to about 35 wt. % of said fatty acid wherein the ratio of said quaternary ammonium compound to said salt is from about 2:1 to about 1:2 on a weight basis .
4. The method of claim 1 where said quaternary ammonium compound is a compound of formula (I) or wherein at least one of the R, R1 and R2 groups is a branched chain or linear, aliphatic saturated or unsaturated hydrocarbon group having from about 12 to about 22 carbon atoms and the balance, if any, of said R, R1 and R2 groups is a lower alkyl group.
5. The method of claim 4 where A is a lower alkyl sulfate group; and where said at least one of the R, R1 and R2 groups is saida saturated hydrocarbon group, it is saturated .
6. As a composition of matter, a solvent free mixture of a quaternary ammonium compound having the formula:
Figure USRE037555-20020219-C00020
where R, R1 and R2 are
(1) linear or branched chain aliphatic saturated or unsaturated hydrocarbon group having up to about 22 carbon atoms;
(2) a hydroxy lower alkyl group;
(3) an alkyl amido alkylene group of the formula,
Figure USRE037555-20020219-C00021
where R4 is lower alkylene and R3 is any of R, R1 or R2;
(4) a lower alkoxy group;
(5) a poly(oxyloweralkylene) group; so that at least one of R, R1 or R2 is one of said hydrocarbon groups or one of said hydroxy lower alkyl groups,
where R5 is a linear or branched chain aliphatic saturated or unsaturated hydrocarbon group having up to about 22 carbon atoms and ,
R6 is a lower alkylene group,
R7 is lower alkyl group or cyclo lower alkyl group, and
where
Ais an anion;
a linear or branched chain saturated or unsaturated fatty acid having from about 12 to about 22 carbon atoms;
a tertiary amine salt having the formula (I) or (II) where R7 is hydrogen ;
Figure USRE037555-20020219-C00022
and a fatty acid ester having the formula:
Figure USRE037555-20020219-C00023
where R8 is a linear or branched chain, aliphatic saturated or unsaturated group having from about 11 to about 21 carbon atoms.
7. The As a composition of claim 6 where said amine is an imidazoline having the formula matter, a solvent free mixture of a quaternary ammonium compound having the formula:
Figure USRE037555-20020219-C00024
or an amine of the formula:
Figure USRE037555-20020219-C00025
said quaternary ammonium compound has the formula
Figure USRE037555-20020219-C00026
where
R9 is alkyl or alkenyls having about 8 to about 30 carbon atoms;
R10 and R11 are independently hydrogen or alkyl having up to about 4 carbon atoms; and
R12 is alkyl having up to about 4 carbon atoms; and the salts of (III) and (IV) where R12 on the nitrogenatom is hydrogen.
A is an anion;
a linear or branched chain saturated or unsaturated fatty acid having from about 12 to about 22 carbon atoms;
a tertiary amine salt having the formula:
Figure USRE037555-20020219-C00027
and a fatty acid ester having the formula:
Figure USRE037555-20020219-C00028
wherein R7 is a lower alkyl group or cyclo lower alkyl group and R 8 is a linear or branched chain, aliphatic saturated or unsaturated group having from about 11 to about 21 carbon atoms.
8. The composition of any of claims 6 or 7 where said tertiary amine, quaternizing agent and fatty acid are present in an amount of mixture contains about 10 wt. % to about 80 wt. % of said quaternary ammonium compound, about 15 wt. % to about 70 wt. % of said tertiary amine salt, about 1 wt. % to about 70 wt. % of said ester and about 5 wt. % to about 70 wt. % of said fatty acid, and wherein the ratio of said quaternary ammonium compound to said tertiary amine salt, is from about 2:1 to about 1:2 on a weight basis.
9. The composition of any of claims 6 or 7 where said tertiary amine, quaternizing agent and fatty acid are present in an amount so that said mixture contains about 35 wt. % to about 55 wt. % of said quaternary ammonium compound, about 10 wt. % to about 30 wt. % of said tertiary amine salt, about 5 wt. % to about 25 wt. % of said ester and about 15 wt. % to about 35 wt. % of said fatty acid wherein the ratio of said quaternary ammonium compound to said tertiary amine salt, is from about 2:1 to about 1:2 on a weight basis.
10. The mixture of claim 6 where said quaternary ammonium compound is a compound of formula (I) and wherein at least one of said R, R1 and R2 groups is a branched chain or linear, aliphatic saturated or unsaturated hydrocarbon group having from about 12 to about 22 carbon atoms and the balance, if any, of said R, R1 and R2 groups is a lower alkyl group.
11. The mixture of claim 9 10where Ais a lower alkyl sulfate group and where said at least one of said R, R1 and R2 is said a saturated hydrocarbon group it is saturated .
12. A fabric softening article of manufacture comprising a fabric softening amount of any of the mixtures of claims 6 or 7, operatively associated with a substrate that will release said mixture to a fabric under fabric softening conditions.
13. The article of claim 12 where said substrate is a fabric.
14. The article of claim 12 where said substrate is a porous polymeric material.
15. A fabric cleaning composition comprising a detergent in combination with a fabric softening amount of the mixtures of any of claims 6 or 7.
16. The composition of claim 15 where said detergent is a synthetic detergent.
17. The composition of claim 15 where said detergent is a soap.
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Families Citing this family (12)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US5298656A (en) * 1991-03-25 1994-03-29 Lenick Jr Anthony J O Ester quaternary compounds
GB9209170D0 (en) * 1992-04-28 1992-06-10 Unilever Plc Rinse conditioner
US5503756A (en) * 1994-09-20 1996-04-02 The Procter & Gamble Company Dryer-activated fabric conditioning compositions containing unsaturated fatty acid
NZ286025A (en) * 1995-03-01 1997-04-24 Colgate Palmolive Co Laundry detergent concentrates; contains nonionic surfactant and water insoluble oil with a hydrophilic polar group, converts to liquid crystal phase dispersion on dilution
US6287547B1 (en) * 1999-10-12 2001-09-11 Sanyo Chemical Industries, Ltd. Hair treatment composition
US20060234899A1 (en) * 2003-03-05 2006-10-19 H.H. Brown Shoe Technologies Inc. D/B/A Dicon Technologies Hydrophilic polyurethane foam articles comprising an antimicrobial compound
MX2009012912A (en) 2007-06-15 2010-01-14 Ecolab Inc Liquid fabric conditioner composition and method of use.
US8232239B2 (en) * 2010-03-09 2012-07-31 Ecolab Usa Inc. Liquid concentrated fabric softener composition
US8673838B2 (en) 2011-06-22 2014-03-18 Ecolab Usa Inc. Solid concentrated fabric softener composition
US9725679B2 (en) 2014-11-21 2017-08-08 Ecolab Usa Inc. Compositions to boost fabric softener performance
US9506015B2 (en) 2014-11-21 2016-11-29 Ecolab Usa Inc. Compositions to boost fabric softener performance
US9688945B2 (en) 2014-11-21 2017-06-27 Ecolab Usa Inc. Compositions to boost fabric softener performance

Citations (15)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US2474202A (en) 1946-01-10 1949-06-21 Montclair Res Corp Quaternary ammonium compounds and the process of making same
US2583772A (en) 1949-02-12 1952-01-29 Dearborn Chemicals Co Acid and quaternary salts of polyamides
US3686025A (en) 1968-12-30 1972-08-22 Procter & Gamble Textile softening agents impregnated into absorbent materials
US3936537A (en) 1974-11-01 1976-02-03 The Procter & Gamble Company Detergent-compatible fabric softening and antistatic compositions
US4022938A (en) 1974-04-16 1977-05-10 The Procter & Gamble Company Fabric treatment compositions
US4237064A (en) 1978-09-08 1980-12-02 Akzona Incorporated Process for preparing quaternary ammonium compositions
US4238373A (en) 1978-03-06 1980-12-09 The Procter & Gamble Company Process for making detergent compositions containing nitrogenous cationic surfactants
EP0048163A2 (en) 1980-09-17 1982-03-24 Beecham Inc. Fabric conditioning articles and methods of use
US4832856A (en) 1987-03-13 1989-05-23 Henkel Kommanditgesellschaft Auf Aktien Aqueous fabric softener for the treatment of fabrics: containing alkylamine, hydroxyalkylamine or quaternary ammonium derivative and a carboxylic acid
US4844824A (en) 1988-02-08 1989-07-04 The Procter & Gamble Company Stable heavy duty liquid detergent compositions which contain a softener and antistatic agent
US4851141A (en) 1984-12-12 1989-07-25 Colgate-Palmolive Company Concentrated stable nonaqueous fabric softener composition
US4857213A (en) 1988-02-08 1989-08-15 The Procter & Gamble Company Liquid detergent containing conditioning agent and high levels of alkyl sulfate/alkyl ethoxylated sulfate
US4859456A (en) 1985-12-23 1989-08-22 Colgate-Palmolive Company Hair rinse conditioners with superior dry hair feel and high hair luster
EP0345495A2 (en) 1988-05-27 1989-12-13 Henkel Kommanditgesellschaft auf Aktien Fabric softener
EP0345475A1 (en) 1988-05-13 1989-12-13 Hoechst Aktiengesellschaft Process for the production of quaternary ammonium salts of long-chain aliphatic carboxylic acids

Patent Citations (16)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US2474202A (en) 1946-01-10 1949-06-21 Montclair Res Corp Quaternary ammonium compounds and the process of making same
US2583772A (en) 1949-02-12 1952-01-29 Dearborn Chemicals Co Acid and quaternary salts of polyamides
US3686025A (en) 1968-12-30 1972-08-22 Procter & Gamble Textile softening agents impregnated into absorbent materials
US4022938A (en) 1974-04-16 1977-05-10 The Procter & Gamble Company Fabric treatment compositions
US3936537A (en) 1974-11-01 1976-02-03 The Procter & Gamble Company Detergent-compatible fabric softening and antistatic compositions
US4238373A (en) 1978-03-06 1980-12-09 The Procter & Gamble Company Process for making detergent compositions containing nitrogenous cationic surfactants
US4237064B1 (en) 1978-09-08 1986-02-11
US4237064A (en) 1978-09-08 1980-12-02 Akzona Incorporated Process for preparing quaternary ammonium compositions
EP0048163A2 (en) 1980-09-17 1982-03-24 Beecham Inc. Fabric conditioning articles and methods of use
US4851141A (en) 1984-12-12 1989-07-25 Colgate-Palmolive Company Concentrated stable nonaqueous fabric softener composition
US4859456A (en) 1985-12-23 1989-08-22 Colgate-Palmolive Company Hair rinse conditioners with superior dry hair feel and high hair luster
US4832856A (en) 1987-03-13 1989-05-23 Henkel Kommanditgesellschaft Auf Aktien Aqueous fabric softener for the treatment of fabrics: containing alkylamine, hydroxyalkylamine or quaternary ammonium derivative and a carboxylic acid
US4844824A (en) 1988-02-08 1989-07-04 The Procter & Gamble Company Stable heavy duty liquid detergent compositions which contain a softener and antistatic agent
US4857213A (en) 1988-02-08 1989-08-15 The Procter & Gamble Company Liquid detergent containing conditioning agent and high levels of alkyl sulfate/alkyl ethoxylated sulfate
EP0345475A1 (en) 1988-05-13 1989-12-13 Hoechst Aktiengesellschaft Process for the production of quaternary ammonium salts of long-chain aliphatic carboxylic acids
EP0345495A2 (en) 1988-05-27 1989-12-13 Henkel Kommanditgesellschaft auf Aktien Fabric softener

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