EP0315126A2 - Compositions détergentes liquides ayant des propriétés de stabilité et d'adoucissement améliorées - Google Patents

Compositions détergentes liquides ayant des propriétés de stabilité et d'adoucissement améliorées Download PDF

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Publication number
EP0315126A2
EP0315126A2 EP88118188A EP88118188A EP0315126A2 EP 0315126 A2 EP0315126 A2 EP 0315126A2 EP 88118188 A EP88118188 A EP 88118188A EP 88118188 A EP88118188 A EP 88118188A EP 0315126 A2 EP0315126 A2 EP 0315126A2
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Prior art keywords
composition according
anionic
weight
alkyl
softening
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EP0315126A3 (fr
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Heidrun E. Maaser
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Colgate Palmolive Co
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Colgate Palmolive Co
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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
    • C11D3/00Other compounding ingredients of detergent compositions covered in group C11D1/00
    • C11D3/0005Other compounding ingredients characterised by their effect
    • C11D3/001Softening compositions
    • C11D3/0015Softening compositions liquid
    • 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
    • C11D1/835Mixtures of non-ionic with cationic 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
    • C11D1/86Mixtures 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
    • C11D3/00Other compounding ingredients of detergent compositions covered in group C11D1/00
    • C11D3/40Dyes ; Pigments
    • C11D3/42Brightening agents ; Blueing agents
    • 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
    • C11D1/12Sulfonic acids or sulfuric acid esters; Salts thereof
    • C11D1/14Sulfonic acids or sulfuric acid esters; Salts thereof derived from aliphatic hydrocarbons or mono-alcohols
    • 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
    • C11D1/12Sulfonic acids or sulfuric acid esters; Salts thereof
    • C11D1/22Sulfonic acids or sulfuric acid esters; Salts thereof derived from aromatic 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
    • C11D1/02Anionic compounds
    • C11D1/12Sulfonic acids or sulfuric acid esters; Salts thereof
    • C11D1/29Sulfates of polyoxyalkylene 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
    • C11D1/62Quaternary 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
    • C11D1/662Carbohydrates or derivatives
    • 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
    • C11D1/72Ethers of polyoxyalkylene glycols

Definitions

  • the present invention relates to novel heavy duty softergent liquid compositions comprising at least 10% nonionic surfactant, and preferably about 6-9% of higher alkyl dimethyl 2-ethyl hexyl quaternary softening compound in conjunction with about 0.1-1% of an anionic optical brightener, to improve low temperature product stability and softening properties. It is preferable to add an anionic surfactant in the molar ratio of 1:1 anionic surfactant:cationic softening compound, and about 4-8% by weight of a lower mono-or di-hydric alcohol.
  • cationic quaternary ammonium compounds as softeners for textile products is very well known in the art. It is also well known to employ such materials for their softening effects during the laundering operation and particularly in the rinse cycle of the laundering process. This latter technique has been necessitated by the fact that the aforesaid quaternary compounds heretofore employed, being mainly cationic in nature, form a complex with the anionic detergent, one of the major types of detergents used in the washing cycle.
  • the use of the quaternary softening agent in the rinse cycle is burdensome to the consumer. Consequently, detergents have been combined with the compatible fabric softeners for use in the wash cycle of the laundering operation.
  • U.S. Patent No. 4,134,838 discloses a fabric conditioning composition
  • a softening agent which include prior art cationic quaternary ammonium compounds such as di-tallow dimethyl anionic chloride and trimethyl tallow ammonium chloride, and a deodorant perfume to which may be added water soluble detergent actives well known in the art such as anionic, nonionic, etc.; inorganic or organic detergent builders; optical brighteners; oils and fragrances; antistatic agents; germicides; bodying agents; soil release agents; ironing aids; bleaches; enzymes; etc.
  • the conditioning compound may be in the form of a solid or liquid composition.
  • the illustrated aqueous liquid fabric conditioning compositions contain a maximum of 6% by weight of the cationic softening agent (Example 1).
  • U.S. Patent No. 4,341.644 discloses a textile softener composition comprising a quaternary ammonium salt mixture dispersed in an aqueous medium where the 4 radicals contain a total of 40-75% saturated aliphatic straight chains, 5-45% unsaturated aliphatic chains and 3-55% branched aliphatic chains.
  • European Patent No. 0,074,056 discloses a liquid softening/rinsing agent for laundry consisting of an aqueous solution or dispersion of a quaternary ammonium compound, wherein two of the radicals are methyl-branched alkyl or alkenyl radicals having 12-30 carbons, and the other two radicals are C1-C4 alkyl groups.
  • U.S. Patent Number 4,569,800 and 4,675,118 disclose a fabric softening composition comprising a quaternary ammonium compound, wherein one radical is a higher aliphatic radical, another radical is 2-ethyl hexyl, and the remaining two radicals are methyl radicals, dissolved in ethanol, water, isopropyl alcohol and blends thereof.
  • a C6-C18 alkyl - ethyl hexyl dimethyl quaternary ammonium salt as a softening agent in a liquid softergent composition comprising an anionic optical brightener and a nonionic-anionic surfactant system provides product stability at low temperatures (40°F) as well as at room temperature and provides increased softening properties to fabrics treated therewith.
  • the advantage of this compound is that it improves low temperature stability of softergent formulations while softening as effectively or more so then a mono tallow trimethylammonium salt.
  • softergents have been troubled by low temperature stability when quaternary ammonium salts were present in conjunction with anionic optical brighteners.
  • Another object of the invention is to provide a stable heavy duty liquid softergent composition, that simultaneously cleanses and softens fabrics during the laundering process comprising an anionic optical brightener, a C6-C18 alkyl 2-ethyl hexyl dimethyl quaternary ammonium softening compound, and a nonionic surfactant in an aqueous medium.
  • Still another object of the invention is to provide a stable liquid softergent formulation having improved cleaning and fabric softening properties, due to the presence of a C6-C18 alkyl 2-­ethyl hexyl dimethyl ammonium quaternary softening compound in a composition comprising an optical brightener, a nonionic surfactant, and preferably an anionic surfactant in a 1:1 molar ratio with said quaternary compound.
  • the liquid softergent composition for laundering fabrics of this invention comprises an effective amount of a higher alkyl 2-ethyl hexyl dimethyl quaternary ammonium softening compound to provide product stability and softening properties in the presence of an anionic optical brightener, and a surfactant system comprising at least 10% by weight of a nonionic surfactant in an aqueous carrier, preferably containing about 4-8% by weight of a lower mono- or di-hydric alcohol; and the method of simultaneously cleansing and softening fabrics without reducing softening, brightener and detergency performance which comprises treating fabrics with said composition during the wash cycle of the laundering operation.
  • present invention relates to a stable heavy duty liquid softergent composition
  • a stable heavy duty liquid softergent composition comprising preferably about 6-9% by weight of a C6-C18 alkyl 2-ethyl hexyl dimethyl quaternary ammonium softening compound, about 0.1-1% by weight of an anionic optical brightener, a surfactant system comprising about 10-30% by weight of a nonionic surfactant, and preferably a lesser amount of an anionic surfactant preferably in a 1:1 molar ratio with said quaternary compound, in an aqueous vehicle, preferably containing about 4-8% by weight of a lower mono- or di-­hydric alcohol.
  • the most preferred molar ratio is 1:1 anionic to cationic, minor variations thereof may be used with large amounts of brightener to obtain stability properties.
  • the nonionic surfactants for use as the fabric detergent are commercially well known and include the ethoxylates and glycosides and mixtures thereof, such as the primary aliphatic alcohol ethoxylates, secondary aliphatic alcohol ethoxylates, alkylphenol ethoxylates, the alcohol ethylene oxide-propylene oxide condensates such as Plurafacs (Wyandotte), C1-30 alkyl monoglycosides and polyglycosides, and mixtures thereof.
  • the ethoxylates and glycosides and mixtures thereof such as the primary aliphatic alcohol ethoxylates, secondary aliphatic alcohol ethoxylates, alkylphenol ethoxylates, the alcohol ethylene oxide-propylene oxide condensates such as Plurafacs (Wyandotte), C1-30 alkyl monoglycosides and polyglycosides, and mixtures thereof.
  • the nonionic synthetic organic detergents are generally the condensation product of an organic aliphatic or alkyl aromatic hydrophobic compound and hydrophilic ethylene oxide group, or a hydrophilic glycoside group containing 1 to about 10 saccharide radicals.
  • any hydrophobic compound having a carboxy, hydroxy, amido or amino group with a free hydrogen attached to the nitrogen can be condensed with ethylene oxide or with the polyhydration product thereof, polyethylene glycol, to form a nonionic detergent.
  • the length of the polyethenoxy chain can be adjusted to achieve the desired balance between the hydrophobic and hydrophilic elements.
  • the nonionic detergents include the polyethylene oxide condensate of one mole of alkyl phenol containing from about 6 to 12 carbon atoms in a straight-or branched-chain configuration with about 5 to 30 moles of ethylene oxide, for example, nonyl phenol condensed with 9 moles of ethylene oxide, dodecyl phenol condensed with 15 moles of ethylene oxide. Condensation products of the corresponding alkyl thiophenols with 5 to 30 moles of ethylene oxide are also suitable.
  • nonionic detergent class also included in the nonionic detergent class are the condensation products of a higher alcohol (e.g. an alkanol containing about 8 to 18 carbon atoms in a straight or branched-­chain configuration) condensed with about 4 to 30 moles of ethylene oxide, for example, lauryl-myristyl alcohol condensed with about 16 moles of ethylene oxide.
  • a commercially available preferred group is the narrow range ethoxylate nonionics known as Tergitol provided by Union Carbide, wherein the ethylene oxide chain (including the terminal ethanol) is of such narrow distribution that at leas 80% and preferably 85-90% of the nonionic detergent contains an average of 4-12 and preferably 6-7 ethylene oxides.
  • the alkyl glycosides may be represented by the following formula, RO(R′O) xZn , wherein R is a C1-C30 alkyl radical, (R′O) is an ethoxy, propoxy or glyceryl group, X has a numerical value of 0-10 and preferably 0, Z is a reducing saccharide containing 5 or 6 carbon atoms, and n has a numerical value of 1-10 and preferably 1 to 3.
  • the hydrophobic alkyl group may be saturated or unsaturated, branched or straight chain, preferably saturated and linear, containing 1 to 30 carbon atoms, preferably 8 to 23 carbon atoms.
  • Suitable alkyl polyglycosides include methyl, ethyl, propyl, octyl, nonyl, decyl, undecyl, dodecyl, tridecyl, tetradecyl, hexdecyl, heptadecyl, octadecyl and mixtures thereof, monoglycosides, diglycosides, triglycosides, tetraglycosides, penta-glycosides, hexaglycosides, etc.
  • the glycoside units may be glucose, galactose, mannose, lactose and/or fructose.
  • Neodol ethoxylates are higher aliphatic alcohol ethoxylates having about 5 to 20 ethylenoxy groups per mole of aliphatic alcohol containing about 10-18 carbon atoms, such as C12-­C13 alkanol condensed with 6.5 moles ethylene oxide, C12-C15 alkanol condensed with 12 moles ethylene oxide, C14-C15 alkanol condensed with 13 moles ethylene oxide, and the like.
  • Neodol ethoxylates Shell Co.
  • nonionic surfactants improve oily soil detergency and provide low temperature (40°F) stability to the softergent composition.
  • Ethoxamers having a HLB (hydrophobic lipophilic balance) value of about 8-15 gives good O/W emulsification, whereas ethoxamers with low HLB values (Below 8) contain less than 5 ethylenoxy groups, and are poor emulsifiers and poor nonionic detergents.
  • the amount of nonionic detergent constitutes the major detergent component in this softergent, about 10-30% and preferably 15-25% by wt. of the composition.
  • the anionic surfactants which are optionally preferred in the softergent of this invention, are commerically well known and include alkylbenzene-sulfonic acid and its salts, e.g. compounds of the formula alkyl-phenol -SO -M, wherein alkyl is an alkyl radical of C8 to C22 and preferably C10 to C18 and M is hydrogen or an alkali metal, which compounds comprise a well-known class of anionic detergents and include sodium dodecyl benzene sulfonate, potassium dodecylbenzenesulfonate, sodium laurylbenzenesulfonate, sodium cetylbenzene sulfonate.
  • alkylbenzene-sulfonic acid and its salts e.g. compounds of the formula alkyl-phenol -SO -M, wherein alkyl is an alkyl radical of C8 to C22 and preferably C10 to C18 and M is hydrogen or an alkali metal, which compounds
  • paraffin sulfonates alkyl sulfates, alcohol ether sulfates, olefin sulfonates and the alkylphenolethoxylate sulfates (e.g. sodium, dinonylphenoxynonaethoxyethanol sulfate), and other equivalent water-soluble salts, particularly of the alkali metal series.
  • the preferred compounds include those which are biodegradable and which are particularly characterized by a linear alkyl substituent of from C10 to C22 and preferably from C12 to C15. It is, of course, understood that the carbon chain length represents, in general, an average chain length since the method for producing such products usually employs alkylating reagents of mixed chain length.
  • substantially pure olefins as well as alkylating compounds used in other techniques can and do give alkylated benzene sulfonates wherein the alkyl moiety is substantially (i.e., at least 99%) of one chain length, i.e., C2 to C12, C13, C14 or C15.
  • the linear alkyl benzene sulfonates are further characterized by the position of the benzene ring in the linear alkyl chain with any of the position isomers (i.e., alpha to omega) being operable and contemplated.
  • benzene sulfonates may also employ the lower alkyl (C1 to C4) analog of benzene such as toluene, xylene, the trimethyl benzenes, ethyl benzene, isopropyl benzene and the like.
  • the sulfonates are generally employed in the water soluble salt form which include as the cation, the alkali metals, ammonium and lower amine, and alkanolamine cations.
  • linear alkyl benzene sulfonates examples include: sodium n-decyl benzene sulfonate sodium n-dodecyl benzene sulfonate sodium n-tetradecyl benzene sulfonate sodium n-pentadecyl benzene sulfonate sodium n-hexadecyl benzene sulfonate and the corresponding lower alkyl substituted homologues of benzene as well as the salts of the cations previously referred to.
  • Mixtures of these sulfonates may, of course, also be used with mixtures which may include compounds wherein the linear alkyl chain is smaller or larger than indicated herein provided that the average chain length in the mixture conforms to the specific requirements of C10 to C22.
  • the linear paraffin sulfonates are also a well-known group of compounds and include water-soluble salts (alkali metal, amine, alkanolamine, and ammonium) of: 1-decane sulfonic acid 1-dodecane sulfonic acid 1-tridecane sulfonic acid 1-tetradecane sulfonic acid 1-pentadecane sulfonic acid 1-hexadecane sulfonic acid as well as the other position isomers of the sulfonic acid group.
  • water-soluble salts alkali metal, amine, alkanolamine, and ammonium
  • paraffin sulfonates In addition to the paraffin sulfonates illustrated above, others with the general range of C10 to C22 alkyl may be used, with the most preferable range being from C12 to C20.
  • the linear alkyl sulfates which are contemplated in this invention comprise the range of C10 to C20.
  • Specific examples include sodium n-decyl sulfate; sodium n-dodecyl sulfate; sodium n-hexadecyl sulfate, sodium n-heptadecyl sulfate; sodium n-­octadecyl sulfate; and the ethoxylated (1 to 100 moles ethylene oxide) derivatives such as the ethoxylated alcohol sulfate and, of course, the other water-soluble salt-forming cations mentioned above.
  • olefin sulfates including long chain alkylene sulfonates, long chain hydroxyalkane sulfonates, as well as disulfonates.
  • suitable olefin which are merely illustrative of the general class, are sodium dodecenyl-1 sulfonate, sodium tetradecyl-1 sulfonate, sodium hexadecenyl-1 sulfonate, and sodium octadecenyl-­1 sulfonate.
  • the amount of anionic surfactant utilized in present composition is less than the nonionic surfactant content by wt, and preferably in a 1:1 molar ratio with the cationic quaternary softening agent, and constitutes the 3.8-7% by wt. of the softergent composition.
  • the presence of the anionic surfactant in the formulation enhances detergency performance and brightening efficacy by depositing the brightener on the fabric more effectively.
  • the essential ingredient in the instant liquid softergent is the cationic fabric softener which is an alkyl 2-ethyl hexyl dimethyl quaternary ammonium compound represented by the following formula: wherein R is an aliphatic straight chain, saturated and unsaturated hydrocarbon radical having from 6 to 18 carbon atoms, and X is a water soluble salt forming anion such as halide, i.e. chloride, bromide, iodide; sulfate, methosulfate, ethosulfate, citrate, acetate, hydroxide, phosphate, or similar inorganic or organic solubilizing radical.
  • halide i.e. chloride, bromide, iodide
  • sulfate, methosulfate, ethosulfate citrate, acetate, hydroxide, phosphate, or similar inorganic or organic solubilizing radical.
  • the R radical is obtained from a mixture of long chain fatty acids such as the tallow or coco radicals.
  • the tallow radical is a mixture of aliphatic saturated and unsaturated hydrocarbon radicals containing a major amount of 16 to 18 carbon chains and a minor amount of 12 to 14 carbon chains.
  • the coco radical is a mixture of saturated and unsaturated hydrocarbon radicals containing a major amount of 12 to 14 carbon chains and a minor amount of 6 to 10 and 16 to 18 carbon chains.
  • Hydrogenated tallow is another preferred long chain radical.
  • suitable radicals include stearyl, cetyl, lauryl, dodecyl, octadecyl, myristyl and hexadecyl and mixtures thereof.
  • Aforesaid alkyl 2-ethyl hexyl dimethyl quaternary ammonium softening compounds is preferably used at levels of 6-9% by weight of the liquid softergent but may be used at 3-4% levels provided effective softening properties are obtained.
  • prior art quaternary softeners are conventionally used at concentrations of 3%.
  • the branched alkyl radical, 2-ethyl hexyl provides the quaternary compound with greater solubility in the aqueous alcoholic medium.
  • the stability of the liquid softergent is also a function of the amount of the quaternary compound in relation to the anionic optical brightener content.
  • a greater quantity of quaternary compound requires a lesser amount of brightener.
  • the anionic optical brighteners have a tendency to form a complex with the cationic quaternaries in an aqueous medium.
  • due to the stearic hindrance in the higher alkyl 2-ethyl hexyl dimethyl ammonium salt it is more difficult for any anionic molecule to approach the cationic ammonium salt, thereby slowing down or preventing complex formation.
  • an anionic optical brightener having a sulfonate moiety such as substituted disulphonated diaminostilbene and triazole compounds to provide brightness to the washed fabric, a feature found desirable to consumers.
  • Optical brighteners are substantive to textiles during the laundering process and sometimes are of comparatively low solubilities. Accordingly, it is important that they be maintained in solution in the liquid softergent composition and readily dispersed in the wash water in order to produce a uniformly bright appearance. Relatively small quantities of brighteners should be used so as not to exceed the limits of solubility.
  • a cationic quaternary softening compound forms a complex with the anionic optical brightener causing low temperature instability of the liquid composition. Due to the increased stearic hindrance in the particular ammonium salt used in present softergent composition, it is more difficult for the anionic molecule to approach, thereby slowing down or preventing complex formation.
  • Certain brighteners have been found to readily dissolve in an aqueous medium and thus are suitable for incorporation in present liquid softergent. Fortunately, these preferred brighteners include both cotton and amide-polyester-brighteners.
  • suitable commercial brighteners are used in present liquid softergents including Tinopal UNPA, Tinopal CBS, Tinopal 5BM(Ciba-Geigy), Arctic White CC, Arctic White CWD (Hilton Davis), and the following Phorwhites from Verona: BHC, BKL, BUP, BBH solution, BRV solution, DCR liquid, DCBVF, EV liquid, DBS liquids and ANR.
  • the anionic optical brightener content of the liquid softergent composition is about 0.1-1%, and preferably about 0.4-­0.8% by weight of the composition. Said concentrations are soluble in the present liquid softergents and are effective in brightening the washed laundry.
  • the liquid vehicle or carrier for the present liquid softergent composition is primarily an aqueous medium. It is preferable to add about 4-8% by weight of a lower alkyl mono- or di-hydric alcohol such as ethanol, propanol, isopropanol, butanol, isobutanol, ethylene glycol, propylene glycol or the like, to control the viscosity of said clear liquid softergent composition, when necessary or desirable.
  • a lower alkyl mono- or di-hydric alcohol such as ethanol, propanol, isopropanol, butanol, isobutanol, ethylene glycol, propylene glycol or the like
  • the softergent composition of the instant invention may also include minimal amounts up to 5% by weight of conventional laundering additives such as germicides, soil suspending agents, antiredisposition agents, coloring materials (dyes and pigments), perfumes, hydrotropes such as sodium and potassium xylene sulfonates, sodium and potassium toluene sulfonates, cumene sulfonates, ethyl benzene sulfonate and the like, enzymes, and enzyme stabilizers, provided they do not interfere with the stability, brightness, detergency and softening activity of the composition.
  • conventional laundering additives such as germicides, soil suspending agents, antiredisposition agents, coloring materials (dyes and pigments), perfumes, hydrotropes such as sodium and potassium xylene sulfonates, sodium and potassium toluene sulfonates, cumene sulfonates, ethyl benzene sulfonate and the like, enzymes, and
  • the present liquid softergent compositions may be prepared by simply admixing the various ingredients at room temperature, in an aqueous medium until a clear liquid is formed.
  • the order of addition of the ingredients may be varied without adversely affecting the formation of the single phase, clear liquid products of instant invention.
  • the softergent composition of the present invention exhibits many desirable characteristics with regard to both physical properties and performance in use. More specifically the liquid compositions are clear, pourable and free-flowing from any suitable container. They are stable upon aging at room temperature (about 70°F) as well as at low temperatures (40°F), without any appreciable precipitation or cloudiness. The present softergents simultaneously and effectively clean, soften and control the static of the different fabrics during the wash cycle of the laundering operation.
  • Liquid Softergent Ingredients % C12-C15 Alcohol 7EO (ethylene oxide) 21.0 Dodecylbenzene sulfonate (DBS) 3.8 Tallow alkyl 2-ethyl hexyl dimethyl ammonium methyl sulfate (TL8-MS) 6.0 Tinopal UNPA* 0.4 Ethanol 6.0 Sodium xylene sulfonate (SXS) 5.0 Water q.s. *CAS Registry No.
  • This composition is prepared by mixing the above water soluble ingredients until a homogeneous, clear liquid softergent is formed which is stable at room temperature and at 40°F.
  • Table I compares compositions containing the prior art monotallow trimethyl ammonium chloride softening agent in lieu of the tallow 2-ethyl hexyl dimethyl ammonium methyl sulfate softening agent in Example 1, using liquid Bold (containing ditallow dimethyl ammonium chloride) as the control having the greatest softness (9.5).
  • Table I lists the comparative softness rating which is within a range of 1 (hardest) to 10 (softest), and the comparative antistatic rating wherein the control exhibits no static Table I Product Softening Antistatic Example 1 8.0 None Monotallow trimethyl ammonium chloride 5.0 Very light Control 9.5 None
  • the rating description for the antistatic is as follows: None-no noise/no cling Very light-1 or 2 items sticking together or 1 type of fabric clinging.
  • Example 1 was ranked equal in softness to liquid Bold at the 99% confidence level.
  • the softness Ranking procedure is as follows: A panel of twenty subjects was asked to rank from harshest to softest, terry hand towels washed 5 times in the products being tested. More than one product can be ranked in the same position. The results are analyzed by Friedman two way non parametric statistical methods, M. Hollander and D.A. Wolf, J. Wiley and Sons, 1973, page 13. The test conditions are a temperature of 72 F and a humidity of 50%.
  • the soil removal (SR) is the sum total of the Rd readings on all the swatches, and the soil removal index (SR1) is the average of the total Rd readings divided by the number of swatches.
  • Table II SR1 Ex. 1 Liquid Fab Liquid Bold 120°F 200 219 189 70°F 201 205 183
  • Example 1 exhibits superior detergency to liquid Bold. No statistically significant difference in detergency was observed between Example 1, and Liquid Fab at 120°F and 70°F. The difference observed at 120°F was due to a better performance of liquid Fab on TFN and TFC fabrics. However, performance on PC cotton, DC and EMPA were equivalent.
  • Example 1 A five week bundle test tested the Example 1 formulation against liquid Bold. On Whites, Example 1 showed a strong win over liquid Bold visually with a preference ratio of 2.74. On cotton, Example 1 showed enhanced performance relative to liquid Bold as measured instrumentally. Rd values for cotton for the two products were not significantly different. On colors, Example 1 was visually preferred over liquid Bold at a ratio of 1.5. No significant difference was detected instrumentally. Liquid Bold showed a strong win on whites and cottons with respect to softness. Static cling evaluation showed liquid Bold to have none and Example 1 to have slight to none.
  • optical brightener can be used in a liquid softener containing the particular quaternary ammonium softening compounds set forth herein and an anionic surfactant in a 1:1 molar ratio, without interfering with the stability of the softergent product. This eliminates the need to limit the brightener content to a minimal amount of about 0.3% or less in order to avoid or prevent instability and the loss of brightening properties.
  • alkyl 2-ethyl hexyl dimethyl quaternary ammonium compound can be used in a liquid softergent composition in an amount in excess of 6% by weight, provided a molar ratio of about 1:1 anioic:quaternary is present, contrary to the prior art usage of a quaternary softening agent in an amount of about 4% by weight, without interfering with the stability of the composition (Examples 19, 20 and 21). There was an insufficient amount of anionic surfactant with reference to the amount of the quaternary compound in Examples 22-27. Composi­tions containing 0.6 by weight of brightener and 7.0% by weight quaternary are stable at 40°F up to 4 weeks.
  • Table III Low Temperature Stability Tallow 2-ethylhexyl quat Brightener Stability at 40 F % % % 6.0 0.4 Passed 6.0 0.8 Passed 7.0 0.4 Passed 7.0 0.6 Passed Tallow trimethyl quat 6.5 0.2 Passed 6.5 0.3 Failed 7.0 0.2 Passed 7.0 0.3 Failed
EP88118188A 1987-11-05 1988-11-02 Compositions détergentes liquides ayant des propriétés de stabilité et d'adoucissement améliorées Withdrawn EP0315126A3 (fr)

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US11727487A 1987-11-05 1987-11-05
US117274 1993-09-07

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EP0315126A3 EP0315126A3 (fr) 1990-03-21

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AU (1) AU619502B2 (fr)
CA (1) CA1315638C (fr)
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NZ (1) NZ226879A (fr)

Cited By (8)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
EP0499282A1 (fr) * 1991-02-15 1992-08-19 Hoechst Aktiengesellschaft Concentré aqueux contenant au moins un composé de type alkyl ou alkényl ammonium
WO1994020596A1 (fr) * 1993-03-08 1994-09-15 Henkel Kommanditgesellschaft Auf Aktien Compositions aqueuses d'adoucissants textiles
WO2001046363A1 (fr) * 1999-12-22 2001-06-28 Unilever Plc Procede de preparation de compositions d'adoucissement de textiles
EP1249488A1 (fr) * 2001-04-11 2002-10-16 Kao Corporation Composition adoucissante
WO2011088089A1 (fr) 2010-01-12 2011-07-21 The Procter & Gamble Company Intermédiaires et tensioactifs utiles dans des compositions de nettoyage ménager et d'hygiène personnelle, et leurs procédés de fabrication
WO2012112828A1 (fr) 2011-02-17 2012-08-23 The Procter & Gamble Company Sulfonates d'alkylphényle linéaires d'origine biologique
WO2012138423A1 (fr) 2011-02-17 2012-10-11 The Procter & Gamble Company Compositions comprenant des mélanges de sulfonates d'alkylphényle c10-c13
WO2014138141A1 (fr) 2013-03-05 2014-09-12 The Procter & Gamble Company Compositions de sucre mélangées

Families Citing this family (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
AU616438B2 (en) * 1987-10-27 1991-10-31 Colgate-Palmolive Company, The Antistatic and fabric softening liquid detergent composition

Citations (4)

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Publication number Priority date Publication date Assignee Title
US4569800A (en) * 1983-07-21 1986-02-11 Akzona Incorporated Quaternary ammonium salts useful as fabric softeners
FR2571736A1 (fr) * 1984-10-17 1986-04-18 Colgate Palmolive Co Composition detergente liquide assouplissante et antistatique et son application au nettoyage de tissus
US4675118A (en) * 1983-07-21 1987-06-23 Akzona Incorporated Quaternary ammonium salts useful as fabric softeners
GB2185992A (en) * 1986-01-30 1987-08-05 Colgate Palmolive Co Liquid softening detergent composition containing alkyl glycoside

Patent Citations (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US4569800A (en) * 1983-07-21 1986-02-11 Akzona Incorporated Quaternary ammonium salts useful as fabric softeners
US4675118A (en) * 1983-07-21 1987-06-23 Akzona Incorporated Quaternary ammonium salts useful as fabric softeners
FR2571736A1 (fr) * 1984-10-17 1986-04-18 Colgate Palmolive Co Composition detergente liquide assouplissante et antistatique et son application au nettoyage de tissus
GB2185992A (en) * 1986-01-30 1987-08-05 Colgate Palmolive Co Liquid softening detergent composition containing alkyl glycoside

Cited By (12)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
EP0499282A1 (fr) * 1991-02-15 1992-08-19 Hoechst Aktiengesellschaft Concentré aqueux contenant au moins un composé de type alkyl ou alkényl ammonium
US5252257A (en) * 1991-02-15 1993-10-12 Hoechst Aktiengesellschaft Water-containing concentrate of at least one alkyl- or alkenyl-substituted ammonium compound
WO1994020596A1 (fr) * 1993-03-08 1994-09-15 Henkel Kommanditgesellschaft Auf Aktien Compositions aqueuses d'adoucissants textiles
WO2001046363A1 (fr) * 1999-12-22 2001-06-28 Unilever Plc Procede de preparation de compositions d'adoucissement de textiles
EP1249488A1 (fr) * 2001-04-11 2002-10-16 Kao Corporation Composition adoucissante
US6770617B2 (en) 2001-04-11 2004-08-03 Kao Corporation Softener composition
WO2011088089A1 (fr) 2010-01-12 2011-07-21 The Procter & Gamble Company Intermédiaires et tensioactifs utiles dans des compositions de nettoyage ménager et d'hygiène personnelle, et leurs procédés de fabrication
US8933131B2 (en) 2010-01-12 2015-01-13 The Procter & Gamble Company Intermediates and surfactants useful in household cleaning and personal care compositions, and methods of making the same
WO2012112828A1 (fr) 2011-02-17 2012-08-23 The Procter & Gamble Company Sulfonates d'alkylphényle linéaires d'origine biologique
WO2012138423A1 (fr) 2011-02-17 2012-10-11 The Procter & Gamble Company Compositions comprenant des mélanges de sulfonates d'alkylphényle c10-c13
US9193937B2 (en) 2011-02-17 2015-11-24 The Procter & Gamble Company Mixtures of C10-C13 alkylphenyl sulfonates
WO2014138141A1 (fr) 2013-03-05 2014-09-12 The Procter & Gamble Company Compositions de sucre mélangées

Also Published As

Publication number Publication date
AU619502B2 (en) 1992-01-30
DK618888A (da) 1989-05-06
NZ226879A (en) 1991-03-26
EP0315126A3 (fr) 1990-03-21
DK618888D0 (da) 1988-11-04
AU2461788A (en) 1989-05-11
CA1315638C (fr) 1993-04-06

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