Classifications

• • C—CHEMISTRY; METALLURGY
  • C11—ANIMAL OR VEGETABLE OILS, FATS, FATTY SUBSTANCES OR WAXES; FATTY ACIDS THEREFROM; DETERGENTS; CANDLES
  • C11D—DETERGENT COMPOSITIONS; USE OF SINGLE SUBSTANCES AS DETERGENTS; SOAP OR SOAP-MAKING; RESIN SOAPS; RECOVERY OF GLYCEROL
  • C11D1/00—Detergent compositions based essentially on surface-active compounds; Use of these compounds as a detergent
  • C11D1/38—Cationic compounds
  • C11D1/65—Mixtures of anionic with cationic compounds
• • C—CHEMISTRY; METALLURGY
  • C11—ANIMAL OR VEGETABLE OILS, FATS, FATTY SUBSTANCES OR WAXES; FATTY ACIDS THEREFROM; DETERGENTS; CANDLES
  • C11D—DETERGENT COMPOSITIONS; USE OF SINGLE SUBSTANCES AS DETERGENTS; SOAP OR SOAP-MAKING; RESIN SOAPS; RECOVERY OF GLYCEROL
  • C11D3/00—Other compounding ingredients of detergent compositions covered in group C11D1/00
  • C11D3/16—Organic compounds
  • C11D3/20—Organic compounds containing oxygen
  • C11D3/22—Carbohydrates or derivatives thereof
  • C11D3/222—Natural or synthetic polysaccharides, e.g. cellulose, starch, gum, alginic acid or cyclodextrin
• • C—CHEMISTRY; METALLURGY
  • C11—ANIMAL OR VEGETABLE OILS, FATS, FATTY SUBSTANCES OR WAXES; FATTY ACIDS THEREFROM; DETERGENTS; CANDLES
  • C11D—DETERGENT COMPOSITIONS; USE OF SINGLE SUBSTANCES AS DETERGENTS; SOAP OR SOAP-MAKING; RESIN SOAPS; RECOVERY OF GLYCEROL
  • C11D3/00—Other compounding ingredients of detergent compositions covered in group C11D1/00
  • C11D3/16—Organic compounds
  • C11D3/20—Organic compounds containing oxygen
  • C11D3/2003—Alcohols; Phenols
  • C11D3/2065—Polyhydric alcohols
• • C—CHEMISTRY; METALLURGY
  • C11—ANIMAL OR VEGETABLE OILS, FATS, FATTY SUBSTANCES OR WAXES; FATTY ACIDS THEREFROM; DETERGENTS; CANDLES
  • C11D—DETERGENT COMPOSITIONS; USE OF SINGLE SUBSTANCES AS DETERGENTS; SOAP OR SOAP-MAKING; RESIN SOAPS; RECOVERY OF GLYCEROL
  • C11D3/00—Other compounding ingredients of detergent compositions covered in group C11D1/00
  • C11D3/16—Organic compounds
  • C11D3/20—Organic compounds containing oxygen
  • C11D3/22—Carbohydrates or derivatives thereof
  • C11D3/222—Natural or synthetic polysaccharides, e.g. cellulose, starch, gum, alginic acid or cyclodextrin
  • C11D3/225—Natural or synthetic polysaccharides, e.g. cellulose, starch, gum, alginic acid or cyclodextrin etherified, e.g. CMC
• • C—CHEMISTRY; METALLURGY
  • C11—ANIMAL OR VEGETABLE OILS, FATS, FATTY SUBSTANCES OR WAXES; FATTY ACIDS THEREFROM; DETERGENTS; CANDLES
  • C11D—DETERGENT COMPOSITIONS; USE OF SINGLE SUBSTANCES AS DETERGENTS; SOAP OR SOAP-MAKING; RESIN SOAPS; RECOVERY OF GLYCEROL
  • C11D3/00—Other compounding ingredients of detergent compositions covered in group C11D1/00
  • C11D3/16—Organic compounds
  • C11D3/20—Organic compounds containing oxygen
  • C11D3/22—Carbohydrates or derivatives thereof
  • C11D3/222—Natural or synthetic polysaccharides, e.g. cellulose, starch, gum, alginic acid or cyclodextrin
  • C11D3/227—Natural or synthetic polysaccharides, e.g. cellulose, starch, gum, alginic acid or cyclodextrin with nitrogen-containing groups
• • C—CHEMISTRY; METALLURGY
  • C11—ANIMAL OR VEGETABLE OILS, FATS, FATTY SUBSTANCES OR WAXES; FATTY ACIDS THEREFROM; DETERGENTS; CANDLES
  • C11D—DETERGENT COMPOSITIONS; USE OF SINGLE SUBSTANCES AS DETERGENTS; SOAP OR SOAP-MAKING; RESIN SOAPS; RECOVERY OF GLYCEROL
  • C11D3/00—Other compounding ingredients of detergent compositions covered in group C11D1/00
  • C11D3/16—Organic compounds
  • C11D3/37—Polymers

Definitions

• This invention relates to liquid cleansing compositions and, more specifically, to aqueous liquid cleansing compositions having desirable foaming, product solubility, viscosity and skin feel characteristics.
• Liquid cleansing products are extensively used as hand cleaners, shampoos, bath foams, shower foams and for many other purposes.
• the present invention is concerned primarily with cleansers used for cleaning skin but is not limited to that application.
• the cleansers of interest are aqueous based and contain a mixture,of surfactants.
• liquid cleansing composition In order to achieve controlled use of a liquid cleansing composition, it is desirable to have a somewhat viscous but pourable or pumpable product. A thin, watery product is too easily spilled and wasted when used and does not have good consumer acceptance.
• a number of high molecular weight polymeric materials have been used in a wide variety of aqueous based products in a thickening, gelling, suspending or protective colloid functionality. Certain nonionic polymers are also known to impart desirable skin feel characteristics to the product, notably guar gum and derivatives thereof (see EP-A-67025).
• cleansing products formulated with the levels of surfactant and polymer necessary to provide satisfactory foaming, thickening and skin feel properties suffer from poor product pourability, solubility and viscosity characteristics, especially on storage at low temperatures as well as diminished thickening and viscosity control under aqueous dilution conditions in for example,shower foam compositions.
• the pourability, solubility and viscosity characteristics are further aggravated by the use of fatty acid alkanolamides which are customarily added to liquid cleansing compositions for suds-boosting purposes.
• liquid cleansing products having desirable foaming, thickening and skin feel properties together with excellent formulation pourability, solubility and viscosity characteristics at both normal and low storage temperatures are provided by the use of polymeric thickening materials, glycerine and a mixed surfactant system comprising additive levels of specified nonionic ethoxylated aliphatic alcohols.
• an aqueous liquid cleansing composition comprising:
• the water-soluble thickening agent useful in the present compositions can be a nonionic or cationic polymeric thickening agent or a mixture thereof.
• Preferred nonionic water-soluble polymers are selected from guar gum, hydroxypropyl guar gum, methyl cellulose, methyl hydroxypropyl cellulose, hydroxyethyl cellulose, hydroxypropyl cellulose, locust bean gum, starch, starch amylose, hydroxyethylamylose and polyoxyethylene.
• the polymer is a high molecular weight material (mass-average molecular weight being generally from about 50,000 to about 5,000,000, preferably from about 100,000 to about 1,000,000), and its thickening ability is preferably such that a 10%, preferably a 5% and more preferably a 1% dispersion of the polymer in water at 20°C exceeds about 1 Pa.s (10 poise) at a shear rate of 10 -2 sec -1 .
• Guar gum is a naturally occurring material which is the principal component of the seed of the'guar plant. Guar gum is extracted from the guar seed and purified. Guar gum is a high molecular weight carbohydrate polymer or polysaccaride made up of mannose and galactose units linked together. The guar molecule is essentially a straight chain of mannose units linked to each other by means of beta (1-4) glycosidic linkages. Galactose units branch from alternate mannose units through alpha (1-6) linkages with the mannose units.
• the desired skin feel of the liquid cleansing products is preferably obtained by using hydroxypropyl guar gum.
• each mannose and galactose unit has from 2-4 hydroxyl groups, depending on where the units are located in the polymer chain.
• Guar gum derivatives are produced by reacting guar gum such that substitution of chemical moieties occurs on some of these hydroxyl groups.
• Hydroxypropyl guar gums are a family of materials with hydroxypropyl groups substituted for some of the hydroxyl groups. The term "degree of substitution" is used to indicate the average number of hydroxypropyl groups which occur on each of the sugar units in the polymer molecule.
• the preferred hydroxypropyl guar gum used in the present invention has a degree of substitution of from about 0.3 to 1.2; especially preferred is hydroxypropyl guar gum with a degree of substitution of about 0.6.
• Such a material is available commercially as Jaguar HP-60 from Meyhall Chemical Ltd.
• Preferred cationic polymeric thickening agents herein are selected from hydroxypropyltrimethylammonium guar gums, quaternized cellulose ethers, homopolymers of dimethyl diallyl ammonium chloride, co-polymers of dimethyl diallyl ammonium chloride and acrylamide, quaternized vinyl pyrrolidone acrylate or methacrylate copolymers of amino alcohol, and polyalkylene imines, in particular the polyethylene imines and the ethoxy polyalkylene imines. Of these, highly preferred are hydroxypropyl tril ⁇ thyl ammonium guar gum, quaternized cellulose ethers and mixtures thereof. Mixtures of the above specified cationic and nonicnic thickening agents are also suitable herein.
• cationic polymers preferred for use herein include cationic guar gums such as hydroxypropyl trimethyl ammonium guar gum (d.s. of from 0.11 to 0.22) available commercially under the trade names Jaguar C-14-S(RTM) and Jaguar C-17(RTM), and also Jaguar C-16(RTM), which contains hydroxypropyl substituents (d.s. of from 0.8-1.1) in addition to the above-specified cationic groups, and quaternized cellulose ethers available commercially under the trade names Ucare Polymer JR and celquat.
• cationic guar gums such as hydroxypropyl trimethyl ammonium guar gum (d.s. of from 0.11 to 0.22) available commercially under the trade names Jaguar C-14-S(RTM) and Jaguar C-17(RTM), and also Jaguar C-16(RTM), which contains hydroxypropyl substituents (d.s. of from 0.8-1.1) in addition to the above-specified cationic groups, and qua
• Suitable cationic polymers are homopolymers of dimethyldiallylammonium chloride available commercially under the trade name Merquat 100, copolymers of dimethyl aminoethylmethacrylate and acrylamide, copolymers of dimethyldiallylammonium chloride and acrylamide available commercially under the trade names Merquat 550 and Merquat S , quaternized vinyl pyrollidone acrylate or methacrylate copolymers of amino alcohol available commercially under the trade name Gafquat, and polyalkyleneimines such as polyethylenimime and ethoxylated polyethylenimine.
• the quantity of polymer material used in the liquid cleansing products of this invention is from about 0.1% to about 2%, especially from about 0.2% to about 1%.
• a preferred range of usage for guar gum and its derivatives is from about 0.3% to about 0.7%.
• the liquid cleansing compositions of this invention comprise a primary surfactant selected from anionic, cationic, zwitterionic and amphoteric surfactants and mixtures thereof, together with an auxiliary surfactant which is a specific type of nonionic surfactant material.
• the primary surfactant comprises from about 8% to about 50%, preferably fran about 10% to about 30%, more preferably from about 15% to about 25% by weight of the composition;
• the auxiliary surfactant comprises from about 0.1% to about 6%, preferably from about 0.5% to about 4%, more preferably from about 1% to about 3% by weight of the composition.
• Suitable anionic surfactants are water-soluble salts of C 8 -C 22 alkyl benzene sulphonates, C 8 -C 22 alkyl sulphates, C 10-18 alkyl polyethoxy ether sulphates, C 8-24 paraffin sulphonates, alpha-C 12-24 olefin sulphonates, alpha-sulphonated C6 - C20 fatty acids and their esters, C 10 -C 18 alkyl glyceryl ether sulphonates, fatty acid monoglyceride sulphates and sulphonates, especially those prepared from coconut oil, C 8 -C 12 alkyl phenol polyethoxy ether sulphates, 2-ac y lox y C 9 -C 23 alkane-l-sulphonate, and beta-alkyloxy C 8 -C 20 alkane sulphonates.
• the anionic surfactant is selected from alkali metal, alkaline earth metal, ammonium, and alkanolammonium salts of alkyl sulphates, alkyl ethoxy sulphates, alkyl benzene sulphonates and mixtures thereof.
• the alkyl sulphate component is preferably a primary alkyl sulphate in which the alkyl group contains about 10-16 carbon atoms, more preferably an average of 12-14 carbon atoms.
• the alkyl group may be linear or branched in configuration.
• Examples of synthetically derived materials include Dobanol 23 (RIM) sold by Shell Chemicals (UK) Ltd, Ethyl 24 sold by the Ethyl Corporation, a blend of C 13 -C 15 alcohols in the ratio 67% C13, 33% C 15 sold under the trade name Lutensol by BASF GmbH and Synperonic (RTM) by ICI Ltd, and Lial 125 sold by Liquichimica Italiana.
• Examples of naturally occurring materials from which the alcohols can be derived are coconut oil and palm kernel oil and the corresponding fatty acids.
• the level of the alkyl sulphate component generally lies in the range of from about 4% to about 20% by weight of the composition, more generally from about 4% to about 16% by weight.
• the usage level lies in the range from about 8% to about 12% by weight, most preferably in the range from about 8% to about 11% by weight.
• the alkyl sulphate level lies in the range from about 12% to about 20%, more preferably from about 14% to about 18% by weight.
• any alkali metal, alkaline earth metal, ammonium or substituted ammonium cation can be used in association with the alkyl sulphate.
• the alkyl sulphate can be associated with a source of magnesium ions either introduced as the oxide or hydroxide to neutralise the acid, or added to the composition as a water soluble salt.
• the magnesium ion will be present at a level of from about 0.001% to about 0.70% by weight, preferably from 0.01% to 0.1% by weight of the composition.
• Alkyl benzene sulphonates preferred for use in compositions of the present invention are those in which the alkyl group, which is substantially linear, contains about 10-16 carbon atoms, preferably about 11-13 carbon atoms, a material with an average chain length of 11.8 being most preferred.
• An alkylbenzene sulphonate content of from about 10% to about 28% by weight of the composition is. generally suitable.
• an alkylbenzene sulphonate content of from 13% to 17% by weight is used.
• the alkyl ethoxy sulphate surfactant component preferably comprises a primary alkyl ethoxy sulphate derived from the condensation product of a C lO -C l6 alcohol with an average of up to 6 ethylene oxide groups.
• the C 10 -C 16 alcohol itself can be obtained from any of the sources previously described for the alkyl sulphate component. It has, however, been found preferable to use alkyl sulphate and alkyl ether sulphate in which the carbon chain length distributions are the same.
• C 12 -C 13 alkyl ether sulphates are preferred and the level of alkyl ethoxy sulphate in the composition lies generally between about 8% and about 25% by weight of the compositions.
• the level of alkyl ethoxy sulphate generally lies in the range from 9% to 15% by weight.
• Blends can be made of material having different degrees of ethoxylation and/or different ethoxylate distributions arising from the specific ethoxylation techniques enployed and subsequent processing steps such as distillation.
• Cationic detergents include those having the formula R ⁇ N(R 2 ) 3 (+) X (-) wherein R is an alkyl chain containing from about 8 to about 20 carbon atoms, each R is selected from alkyl and alkanol groups containing from 1 to 4 carbon atoms and benzyl groups, there being normally no more than one benzyl group and two R 2 groups can be joined by either a carbon-carbon ether, or imino linkage to form a ring structure, and X represents a halogen atom, sulfate group, nitrate group or other pseudohalogen group.
• Specific examples are coconut alkyl trimethyl ammonium chloride, dodecyldimethyl benzyl bromide and dodecyl methyl morpholino chloride.
• Zwitterionic synthetic detergents can be broadly described as derivatives of aliphatic quaternary ammonium, phosphonium, and sulfonium compounds, in which the aliphatic radical may be straight chain or branched, and wherein one of the aliphatic substituents contains from about 8 to 18 carbon atoms and one contains an anionic water solubilizing group, e.g., carboxy, sulfo, sulfato, phosphato, or phosphono.
• Examples of compounds falling within this definition are 3-(N,N-dimethyl-N-hexadecylammonio) propane-l-sulfonate and 3-(N,N-dimethyl-N-hexadecylammonio)-2-hydroxy propane-1-sulfonate.
• Amphoteric synthetic detergents can be broadly described as derivatives of aliphatic secondary and tertiary amines, in which the aliphatic radical may be straight chain or branched and wherein one of the aliphatic substituents contains from about 8 to 18 carbon atoms and one contains an anionic water solubilizing group, e.g., carboxy, sulfo, sulfato, phosphato, or phosphono. Examples of compounds falling within this definition are sodium-3-dodecylaminopropionate and sodium-3-dodecylaminopropane sulfonate.
• R 1 represents alkyl, alkenyl or monohydroxy alkyl radical of from 8 to 18 carbon atoms optionally containing up to 10 ethylene oxide moieties or a glyceryl moiety
• R 2 and R 3 represents alkyl of from 1 to 3 carbon atoms optionally substituted with a hydroxy group, e.g., methyl, ethyl, propyl, hydroxy ethyl, or hydroxy propyl raidcals.
• Examples include dimethyldodecylamine oxide, oleyldi(2-hydroxyethyl) amine oxide, dimethyloctylamine oxide, dimethyltetradecylamine oxide, dimethyldecylamine oxide, 3,6,9-trioxaheptadecyldiethylamine oxide, di(2-hydroxyethyl)-tetradecylamine oxide, 2-dodecoxyethyldimethylamine oxide, 3-dodecoxy-2-hydroxypropyldi (3-hydroxypropyl) -amine oxide, dimethylhexadecylamine oxide.
• the amine oxide surfactants are generally referred to as semi-polar although in acid to neutral media they behave akin to cationic surfactants.
• the auxiliary surfactant component of the invention is a C 6 -C 13 aliphatic alcohol ethoxylate generally containing an average (E av ) of from about 1.5 to about 25, preferably from about 2 to 15 and more preferably from about 6 to about 10 moles of ethylene oxide per mole of alcohol.
• the auxiliary surfactant preferably contains not more than about 1% by weight of unethoxylated alcohol when the ethoxylated alcohol contains an average of less than 9 moles of ethylene oxide and not more than about 2% by weight of unethoxylated alcohol when the ethoxylated alcohol contains an average of 9 or more moles of ethylene oxide per mole of. alcohol.
• Such surfactants are preferred from the viewpoint of low temperature stability, the unethoxylated content preferably being less than about 0.7%, and more preferably less than about 0.5%.
• the unethoxylated material can be removed by vacuum distillation.
• the starting alcohol may be a primary or secondary alcohol but is preferably a primary alcohol which may be derived from natural or synthetic sources.
• natural fats or oils, or products of Ziegler olefin build up reactions or OXD synthesis may all be used as the source of the hydrocarbon chain, the structure of which may be linear or branched in type.
• the preferred alcohol chain length range is from C 9 -C 11 as it has been found that sudsing performance is optimum for ethoxylates made from such alcohols. It is also desirable for performance reasons that the hydrophilic-lipophilic balance (HLB) of the ethoxylated alcohol is in the range from 8.0 to 17.0, more preferably from 11.0 to 17.0 and most preferably from 11.0 to 15.0.
• HLB hydrophilic-lipophilic balance
• compositions of the invention additionally contain from about 0.1% to about 6%, preferably from about 0.5% to about 4%, more preferably from about 1% to about 3% of glycerine.
• the glycerine is valuable herein for improving the physical characteristics of the product.
• the combined use of the polymer, auxiliary nonionic surfactant and glycerine is found to be particularly valuable for achieving optimum product stability, pourability and solubility in aqueous liquors as well as good thickening and viscosity control under dilution conditions.
• the compositions of the invention contain a strong acid-derived electrolyte level of less than about 0.5%, preferably less than about 0.1% for optimum product stability.
• compositions herein have a viscosity (neat) at 24°C in the range from about 1,000 to about 20,000 cps, preferably from about 2,000 to about 15,000 cps, more preferably from about 4,000 to about 12,000 cps, viscosity being measured in a Brookfield LVT viscometer using spindle number 4 at speed 3.
• fatty acid alkanolamides e.g. C 10 -C 16 mono- and di-C 2 -C 3 alkanolamides
• fatty acid alkanolamides e.g. C 10 -C 16 mono- and di-C 2 -C 3 alkanolamides
• the amide is maintained at low concentration in product, preferably no more than about 4% by weight, more preferably less than about 3% by weight.
• the cleansing product be formulated to provide a pH in use within the range of from about 4 to about 10, depending upon the particular surfactant or materials employed. Especially preferred is a pH in the range of 5 to 7. Any of a large number of known substances can be used to adjust the pH of the liquid cleansing product, e.g., sodium hydroxide, citric acid, generally at a level of up to about 0.5% of the product composition. Perfumes may be used in formulating the liquid cleansing products, generally at a level of about 0.1% to about 5% of the product composition. Colorants may also be used in the liquid cleansing products.
• Opacifiers e.g., ethylene glycol distearate, polystyrene latex, generally at a level of about 0.2% to about 2.0% of the product composition, may be used in the liquid cleansing products to provide them with an opaque or pearlescent appearance.
• -Preservatives e.g., EDTA, methyl paraben, propyl paraben, Germall 115, Kathon, generally at a level of less than 1%, may be incorporated in the liquid cleansing products to prevent microbiological growth in the products.
• the liquid cleansing products of the present invention generally contain at least about 42% water, preferably from about 60% to about 90% water.
• the preservative is then added and the premix is heated to about 65°C at which temperature coconut monoethanolamide, if present, is added.
• Ethyleneglycoldistearate is added after further heating to a temperature of about 65°C to 70°C.
• alkyl ether sulphate (supplied as a 28% active) and the remaining alkyl sulphate are added to a main mix tank together with a water slurry of the guar material. Finally the citric acid, and magnesium chloride, if present, are added.
• the premix is then added with agitation at a temperature of about 70°C to the main mix, the combined mixture is rapidly cooled in a heat exchanger and dyes and perfume are added to form the finished product.
• the resulting products have desirable foaming, thickening and skin feel properties together with excellent formulation pourability, solubility and viscosity characteristics at both normal and low storage temperatures as well as good thickening and viscosity control when diluted with water under typical shower foam usage conditions.

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Citations (7)

• 1986
  • 1986-03-04 EP EP86301500A patent/EP0197649B1/de not_active Expired - Lifetime
  • 1986-03-04 DE DE8686301500T patent/DE3671645D1/de not_active Expired - Fee Related
  • 1986-03-05 CA CA000503344A patent/CA1291391C/en not_active Expired - Fee Related
  • 1986-03-06 KR KR1019860001587A patent/KR940000438B1/ko not_active IP Right Cessation

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