CA2127657A1 - High foaming nonionic surfactant based liquid detergent - Google Patents
High foaming nonionic surfactant based liquid detergentInfo
- Publication number
- CA2127657A1 CA2127657A1 CA002127657A CA2127657A CA2127657A1 CA 2127657 A1 CA2127657 A1 CA 2127657A1 CA 002127657 A CA002127657 A CA 002127657A CA 2127657 A CA2127657 A CA 2127657A CA 2127657 A1 CA2127657 A1 CA 2127657A1
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- CA
- Canada
- Prior art keywords
- liquid detergent
- detergent composition
- surfactant
- ethylene oxide
- moles
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Abandoned
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Classifications
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- C—CHEMISTRY; METALLURGY
- C11—ANIMAL OR VEGETABLE OILS, FATS, FATTY SUBSTANCES OR WAXES; FATTY ACIDS THEREFROM; DETERGENTS; CANDLES
- C11D—DETERGENT COMPOSITIONS; USE OF SINGLE SUBSTANCES AS DETERGENTS; SOAP OR SOAP-MAKING; RESIN SOAPS; RECOVERY OF GLYCEROL
- C11D3/00—Other compounding ingredients of detergent compositions covered in group C11D1/00
- C11D3/0005—Other compounding ingredients characterised by their effect
- C11D3/0094—High foaming compositions
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- C—CHEMISTRY; METALLURGY
- C11—ANIMAL OR VEGETABLE OILS, FATS, FATTY SUBSTANCES OR WAXES; FATTY ACIDS THEREFROM; DETERGENTS; CANDLES
- C11D—DETERGENT COMPOSITIONS; USE OF SINGLE SUBSTANCES AS DETERGENTS; SOAP OR SOAP-MAKING; RESIN SOAPS; RECOVERY OF GLYCEROL
- C11D1/00—Detergent compositions based essentially on surface-active compounds; Use of these compounds as a detergent
- C11D1/88—Ampholytes; Electroneutral compounds
- C11D1/94—Mixtures with anionic, cationic or non-ionic 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
- C11D1/00—Detergent compositions based essentially on surface-active compounds; Use of these compounds as a detergent
- C11D1/02—Anionic compounds
- C11D1/12—Sulfonic acids or sulfuric acid esters; Salts thereof
- C11D1/14—Sulfonic acids or sulfuric acid esters; Salts thereof derived from aliphatic hydrocarbons or mono-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
- C11D1/00—Detergent compositions based essentially on surface-active compounds; Use of these compounds as a detergent
- C11D1/02—Anionic compounds
- C11D1/12—Sulfonic acids or sulfuric acid esters; Salts thereof
- C11D1/28—Sulfonation products derived from fatty acids or their derivatives, e.g. esters, amides
-
- 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
- C11D1/02—Anionic compounds
- C11D1/12—Sulfonic acids or sulfuric acid esters; Salts thereof
- C11D1/29—Sulfates of polyoxyalkylene ethers
-
- 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
- C11D1/66—Non-ionic compounds
- C11D1/72—Ethers of polyoxyalkylene glycols
-
- 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
- C11D1/66—Non-ionic compounds
- C11D1/722—Ethers of polyoxyalkylene glycols having mixed oxyalkylene groups; Polyalkoxylated fatty alcohols or polyalkoxylated alkylaryl alcohols with mixed oxyalkylele 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
- C11D1/00—Detergent compositions based essentially on surface-active compounds; Use of these compounds as a detergent
- C11D1/66—Non-ionic compounds
- C11D1/74—Carboxylates or sulfonates esters of polyoxyalkylene glycols
-
- 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
- C11D1/88—Ampholytes; Electroneutral compounds
- C11D1/90—Betaines
Abstract
ABSTRACT OF DISCLOSURE
A high foaming, light duty liquid detergent with desirable cleansing properties and mildness to the human skin comprising: a water soluble nonionic surfactant; a water soluble or dispersible foaming, anionic surfactant; a zwitterionic betainesurfactant.
A high foaming, light duty liquid detergent with desirable cleansing properties and mildness to the human skin comprising: a water soluble nonionic surfactant; a water soluble or dispersible foaming, anionic surfactant; a zwitterionic betainesurfactant.
Description
2127~7 HIGH FOAMING NONIONIC SURFACTANT BASED LIQUID DETERGENT
Background Of The Invention The present invention relates to novel light duty liquid detergent compositions 5 with high foaming properties, containing a nonionic surfactant, a specific group of anionic surfactants, and a Zwitterionic betaine surfactant wherein the surfactants are dissolved in an aqueous medium.
Nonionic surfactants are in general chemically inert and stable toward pH
change and are therefore well suited for mixing and formulation with other matarials.
10 The superior performance of nonionic surfactants on the removal of oily soil is well recognized. Nonionic surfactants are also known to be mild to human skin. However, as a class, nonionic surfactants are known to be low or moderate foamers.
Consequently, for detergents which require copious and stable foam, the application of nonionic surfactants is limited. There have been substantial interest and efforts to 15 develop a high foaming detergent with nonionic surfactants as the major ingredient.
Little has been achieved.
The prior art is replete with light duty liquid detergent compositions containin~
nonionic surfactants in combination with anionic andlor betaine surfactants wherein the nonionic detergent is not the major active surfactant, as shown in U.S. Patent No.
20 3,S58,985 wherein an anionic based shampoo contains a minor amount of a fatty acid alkanolamide U.S. Patent No. 3,769,398 discloses a betaine-based shampoo containing minor amounts of nonionic surfactants. This patent states that the low foaming properties of nonionic detergents renders its use in shampoo compositions non-preferred. U.S. Patent No. 4,329,335 also discloses a shampoo containing a 25 betaine surfactant as the major ingredient and minor amounts of a nonionic surfactant and of a fatty acid mono- or di-ethanolamide. U.S. Patent No. 4,259,204 discloses a shampoo comprising 0.8-20% by weight of an anionic phosphoric acid ester and oneadditional surfactant which may be either anionic, amphoteric, or nonionic. U.S.Patent No. 4,329,334 discloses an anionic-amphoteric based shampoo containing a .,.. , .: :,. :. :.: . , i. - . - , . . . , -F-:; . ~
- 21276~7 major amount of anionic surfactant and lesser amounts of a betaine and nonionic surfactants.
U.S. Patent No. 3,935,129 discloses a liquid cleaning composition based on the alkali metal silicate content and containing five basic ingredients, namely, urea, 5 glycerin, triethanolamine, an anionic detergent and a nonionic detergent. The silicate content determines the amount of anionic and/or nonionic detergent in the liquidcleaning composition. However~ the foaming property of these detergent composifions is not discussed therein.
U.S. Patent No. 4,129,515 discloses a heavy duty liquid detergent for 10 laundering fabrics comprising a mixture of substantially equal amounts of anionic and nonionic surfactants, alkanolamines and magnesium salts, and, optionally, zwitterionic surfactants as suds modifiers.
U.S. Patent No. 4,224,195 discloses an aqueous detergent composition for laundering socks or stockings comprising a specific group of nonionic detergents, 15 namely, an ethylene oxide of a secondary alcohol, a specific group of anionicdetergents, namely, a sulfuric ester salt of an ethylene oxide adduct of a secondary alcohol, and an amphoteric surfactant which may be a betaine, wherein either theanionic or nonionic surfactant may be the major ingredient.
The prior art also discloses detergent compositions containing all nonionic 20 surfactants as shown in U.S. Patent Nos. 4,154,706 and 4,329,336 wherein the shampoo compositions contairi a plurality of particular nonionic surtactants in order to effect desirable foaming and detersive properties despite the fact that nonionicsurfactants are usually deficient in such properties.
U.S. Patent No. 4,013,787 discloses a piperazine based polymer in 25 conditioning and shampoo cornpositions which may contain all nonionic surtactant or all anionic surtactant.
U.S. Patent No. 4,450,091 discloses high viscosity shampoo compositions containing a blend ot an amphoteric betaine surtactant, a 21276~7 62301-1~74 polyoxybutylenepolyoxyethylene nonionic detergent, an anionlc surfactant, a fatty acid alkanolamide and a polyoxyalkylene glycol fatty ester.
United States Patent No. 4,595,526 describes a composition comprising a nonionic surfactant, a betaine surfactant, an anionic surfactant and a C12-C14 fatty acid monoethanolamide foam stabllizer.
However, none of the above-cited patents discloses a hlgh foaming, nonlonic based, liquid detergent composition containing a nonionic surfactant, a supplementary high foaming ethoxylated alkyl ether sulfate anionic surfactant and a supplementary foaming zwitterionic surfactant selected from betaine type surfactants as the three essential ingredients wherein the composition does not contain any amine oxide, calcium carbonate, polymeric or clay thickeners, abrasive, clays, silicas, -~
alkyl glycine surfactant, cyclic imidinium surfactant, or more than 3.0 wt.% of a fatty acld or a metal salt of the fatty acid compounds.
None of the above-cited patents discloses a high -~
foaming, nonionic based, liquid detergent composition containing a - nonionic surfactant as a major active ingredient and lesæer amounts of a magnesium salt of C8-C18 ethoxylated alkyl ether sulfate surfactant, an alkali metal salt of an alkyl sulfate surfactant, and a supplementary foaming zwitterlonic surfactant selected from betalne type surfactants as the four essential ingredients, wherein the nonionic ingredient constitutes more than 50% of the total surfactant content. ;~
2127~.57 Summarv Of The Invention It has now been found that a high foaming liquid detergent can be formulated with a nonionic surfactant which has desirable cleaning properties, mildness to the human skin.
A major object of this invention is to provide a novel, liquid detergent wlth desirable high foaming and cleaning properties which is mlld to the human skln.
Additional ob~ects, advantages and novel features of the invention will be set forth in part in the description which follows, and in part will become apparent to those skilled in the art upon examination of the following or may be learned by practice of the invention. The objects and advantages of ~he invention may be realized and attained by means of the lnstrumentalities and combinations particularly pointed out in the appended claims.
To achieve the foregoing and other objects and in accordance with the purpose of ~he present inventlon, as embodled and broadly described hereln the novel, high foamlng, llght duty llquld detergent of this invention comprises three essential surfactantæ: a water soluble, ethoxylated, nonionic surfactant; a foaming water soluble zwitterionic surfactant selected from the class of betaines; and an ethoxylated alkyl ether sulfate surfactant, wherein the ingredients are dissolved in an aqueous vehicle, and the composition does not contain any amine oxide, alkanolamlde ingredients.
More specifically, the present invention relates to a high foaming, nonionic based, liquid detergent comprising a 2127~
nonlonic surfactant selected from the group consistlng of water soluble primary aliphatic alcohol ethoxylates, secondary allphatic alcohol ethoxylates, alkyl phenol ethoxylates and alcohol ethylene oxide/propylene oxide condensates; a water soluble zwitterionic betaine surfactant; an ethoxylated alkyl ether sulfate surfactant;
and optionally a C8-C14 alkyl sulfate surfactant wherein the lngredlents are dissolved in an aqueous vehicle.
The total amount of surfactants may constitute 10%-55%, preferably 20% - 40%, most preferably 25%-35%, by weight of the liquid composition.
In a first embodiment, the liquid aqueous detergent compositlon of the present invention contains a nonionic surfactant, an ethoxylated alkyl (ether) sulfate anionic surfactant, and a zwitterionic betalne surfactant, and does not contain amine oxides, alkali metal or alkallne earth metal carbonates, polymerlc or clay thickeners, clays, abrasives, alkyl glycine surfactants, cyclic imldinium surfactants, sillcas or more than 3 wt.% of a fatty acid or a metal salt of a fatty acid.
In a second embodiment, the nonionic based, liquid detergent composition of the present invention contains a major amount of the nonionic surfactant supplemented with lesser amounts of a magnesium salt of the ethoxylated alkyl ether sulfate surfactant, a sodium salt of the alkyl sulfate surfactant, and the ~-zwitterionic betalne surfactant, wherein the composltlon does not contain any amine oxlde, fatty acld alkanolamides, clay, silica, abrasive, clay or polymeric thickeners, alkali metal or alkaline earth metal carbonate or more than 3 wt.% of a fatty acid or its , "
s . ,:
2127~57 metal salt.
Detailed DescriPtion Of The Invention In the first embodiment, the high foaming nonionic based light duty liquid detergent composition of the instant invention comprises approximately by weight: 10 to 25 wt.~ of a water soluble nonionic surfactant; 8 to 16 wt.~ of an ethoxylated alkyl ether sulfate; and 2 to 12 wt.% of a betaine surfactant; and the balance (e.g. 47 to 80 wt.%) of water, wherein the composition does not contain any amine oxides, alkali metal or alkaline earth metal carbonates (e.g., calcium carbonate), polymeric or clay thickeners, abrasives, clays, silicas, alkyl glycine surfactants, cyclic imidinium surfactants, or more than 3 wt.% of a fatty acid or a metal salt of the fatty acid.
In the second embodiment, the liquid detergent compositions of the present invention comprises approximately by weight, 10 to 20 wt.%, more preferably 11 to 17 wt.% of a nonlonlc surfactant; 0.5 to 8 wt.% more preferably 1 to 7 wt.% of an alkali metal or ammonium salt of a C8-C14 alkyl sulfate surfactant; 0.5 to 8 wt.% more preferably 1 to 7 wt.% of a -magnesium salt of a C8-C18 ethoxylated alkyl ether sulfate surfactant and 2 to 10 wt.%, more preferably 3 to 9 wt.% of a betaine zwitterionic surfactant, wherein the composition does not contain any amide oxides, fatty acid alkanolamides, alkali metal or alkaline earth metal carbonates, clays, silicaæ, abrasives, clay or polymeric thickeners or more than 3 wt.% of fatty acids or their metals salts.
The nonionic surfactant which constitutes the major ~ 21276~7 ingredient in the liquid detergent composition iæ present ln amounts of 10 to 25%, preferably 15 to 20% by welght of the composition and provides superior performance in the removal of oily soil and mildness to human skln.
5b 2 1 2 7 6 ~ l The water soluble nonionic surfactants utilized in this invention are commercially well known and include the primary aliphatic alcohol ethoxylates, secondary aliphatic alcohol ethoxylates, alkylphenol ethoxylates and ethylene-oxide-propylene oxide condensates on primary alkanols, such a Plurafacs (BASF) and 5 condensates of ethylene oxide with sorbitan fatty acid esters such as the Tweens (ICI).
The nonionic synthetic organic detergents generally are the condensation products of an organic aliphatic or alkyl aromatic hydrophobic compound and hydrophilic ethylene oxide groups. Practically any hydrophobic compound having a carboxy, hydroxy, amido, or amino group with a free hydrogen attached to the nitrogen can be 10 condensed with ethylene oxide or with the polyhydration product thereof, polyethylene glycol, to form a water soluble nonionic detergent. Further, the length of the polyethenoxy hydrophobic and hydrophilic elements.
The nonionic detergent class includes the condensation products of a higher alcohol (e.g., an alkanol containing 8 to 18 carbon atoms in a straight or branched 15 chain configuration) condensed with 5 to 30 moles of ethylene oxide, for example, lauryl or myristyl alcohol condensed with 16 moles of ethylene oxide (EO), tridecanol condensed with 6 to moles of EO, myristyl alcohol condensed with 10 moles of EO per mole ot myristyl alcohol, the condensation product of EO with a cut of coconut fatty alcohol containing a mixture of fatty alcohols with alkyl chains varying from 10 to 14 20 carbon atoms in length and wherein the condensate contains either 6 moles of EO per mole of total alcohol or 9 moles of EO per mole of alcohol and tallow alcohol ethoxylates containing 6 EO to 11 EO per mole of alcohol.
A preferred group of the foregoing nonionic surfactants are the Neodol ethoxylates (Shell Co.), which are higher aliphatic, primary alcohol containing 9-15 25 carbon atoms, such as Cg-C1 1 alkanol condensed with 8 moles of ethylene oxide (Neodol 91-8), C12 13 alkanol condensed with 6.5 moles ethylene oxide (Neodol 23-6.5), C12 15 alkanol condensed with 12 moles ethylene oxide (Neodol 25-12), C14 15 alkanol condensed with 13 moles ethylene oxide (Neodol 45-13), and the like.
21276~7 Such ethoxamers have an HLB (hydrophobic lipophiiic balance) value of 8 to 15 and give good OAN emulsification, whereas ethoxamers with HLB values below 8 containless than ~ ethyleneoxide groups and tend to be poor emulsifiers and poor detergents.
Additional satisfactory water soluble alcohol ethylene oxide condensates are the condensation products of a secondary aliphatic alcohol containing 8 to 18 carbon atoms in a straight or branched chain configuration condensed with 5 to 30 moles of ethylene oxide. Examples of commercially available nonionic detergents of the foregoing type are C1 1-C15 secondary alkanol condensed with either 9 EO (Tergitol 15-S-9) or 12 EO (Tergitol 15-S-12) marketed by Union Carbide.
Other suitable nonionic detergents include the polyethylene oxide condensates of one mole of alkyl phenol containing from 8 to 18 carbon atoms in a straight- or branched chain alkyl group with 5 to 30 moles of ethylene oxide. Specific examples of alkyl phenol ethoxylates include nonyl condensed with 9.5 moles of EO per mole of nonyl phenol, dinonyl phenol condensed with 12 moles of EO per mole of dinonyl phenol, dinonyl phenol condensed with 15 moles of EO per mole of phenol and di- -isoc~ylphenol condensed with 15 moles of EO per mole of phenol. Commercially available nonionic surfactants of this type include Igepal C0-630 (nonyl phenol ethoxylate) marketed by GAF Corporation.
Condensates of 2 to 30 moles of ethylene oxide with sorbitan mono- and tri-C10-C20 all~anoic acid esters having a I~LB of 8 to 15 also may be employed as the nonionic detergent ingredient in the described shampoo. These surfactants are well known and are available from Imperial Chemical Industries under the Tween trade name. Suitable surfactants include polyoxyethylene (4) sorbitan monolaurate, polyoxyethylene (4) sorbitan monostearate, polyoxyethylene (20) sorbitan trioleate and polyoxyethylene (20) sorbitan tristearate.
The water-solubie zwitterionic surfactant, which is also an essential ingredientof present liquid detergent composition, constitutes 2 to 12%, preferably 3 to 10%, by 2~27 ~ra7 weight and provides good foaming properties and mildness to the present liquid detergent. The zwitterionic surfactant is a water soluble betaine having the general formula:
R1 - N - R4 - CO~
wherein R1 is an alkyl group having 10 to 20 carbon atoms, preferably 12 to 16 carbon atoms, or the amido radical:
O H
Il I
R-C - N - (CH2)a~
wherein R is an alkyl group having 9 to 19 carbon atoms and a is the integer 1 to 4; R2 and R3 are each alkyl groups having 1 to 3 carbons and preferably 1 carbon; R4 is an alkylene or hydroxyalkylene group having from 1 to 4 carbon atoms and, optionally, one hydroxyl group. Typical alkyldimethyl betaines include decyl dimethyl betaine or 2-(N-decyl-N, N-dimethyl-ammonia) acetate, coco dimethyl betaine or 2-(N-coco N, N-dimethylammonio) acetate, myristyl dimethyl betaine, palmityl dimethyl betaine, lauryl dimethyl betaine, cetyl dimethyl betaine, stearyl dimethyl betaine, eto. The amidobetaines similarly include cocoamidoethylbetaine, cocoamidopropyl betaine and the like. A preferred betaine is coco (Cg-C1g) amidopropyldimethyl betaine.
The anionic sulfate and sulfonate surfactants which may be used in the detergent of ~his invention are water soluble such as triethanolamine and include the sodium, potassium, ammonium and ethanolammonium salts of Cg-C1g alkyl sulfates such as lauryl sulfate, myristyl sulfate and the like; linear Cg-C16 alkyl benzene sulfonates; C1 o-C20 paraffin sulfonates and alpha olefin sulfonates containing about 10-24 carbon atoms. The preferred sulfate surfactant is a Cg to C14 sulfate and is present in the composition at a concentration of about 0.5 to 8 wt. %.
The paraffin sulfonates may be monosulfonates or di-sulfonates and usually are mixtures thereof, obtained by sulfonating paraffins of 10 to 20 carbon atoms.
2127~7 Preferred paraffin sulfonates are those of C12-1 g carbon atoms chains, and morepreferably they are of C14 17 chains. Paraffin sulfonates that have the sulfonate group(s) distributed along the paraffin chain are described in U.S. Patents 2,503,280; 2,507,088; 3,260,744; and 3,372,188; and also in German Patent 735,096. Such compounds may be made to specifications and desirably the content of paraffin sulfonates outside the C14 17 range will be minor and will be minimized, as will be any contents of di- or poly-sulfonates.
Examples of suitable other sulfonated anionic detergents are the well known higher alkyl mononuclear aromatic sulfonates, such as the higher alkylbenzene sulfonates containing 9 to 18 or preferably 9 to 10 to 15 or 16 carbon atoms in the higher alkyl group in a straight or branched chain, or Cg 1s alkyl toulene sulfonates.
A preferred alkylbenzene sulfonate is a linear alkylbenzene sulfonate having a higher content of 3-phenyl (or higher) isomers and a correspondingly lower content (well below 50%) of 2-phenyl (or lower) isomers, such as those sulfonates wherein the benzene ring is attached mostly at the 3 or higher (for example 4, 5, 6 or 7) position of the alkyl group and the content of the isomers in which the benzene ring is attached in the 2 or 1 position is correspondingly low. Preterred materials are set forth in U.S.
Patent 3,320,174, especially those in which the alkyls are of 10 to 13 carbon atoms.
The ethoxylated alkyl ether sulfate (AEOS.xEO) is depicted by the formula: R-(OCHCHC2)x OSO3M wherein x is about I to 22, more preferably about 1 to about 10and R is an alkyl group having about 8 to 18 carbon atoms and more preferably about 12 to about 15 carbon atoms and natural cuts for example C12-1 4. C12-C1 3 and C1 2-15 and M is an alkali earth metal cation such as magnesium. Examples of satisfactory anionic ethoxylated sulfate are the Cg 18 ethoxylated alkyl ether sulfate salts having the formula: R~(ocH2-H4)n OSO3M wherein R' is alkyl of 8 or 9 to 18carbon atoms, n is 1 to 22, preferably 1 to 5, and M is a magnesium cation. The ethoxylated alkyl ether sulfates may be made by sulfating the condensation product of 21276~7 ethylene oxide and Cg 1 8 alkanol, and neutralizing the resultant product. The ethoxylated alkyl ether sulfates differ from one another in the number of carbon atoms in the alcohols and in the number of moles of ethylene oxide reacted with one mole of such alcohol. Preferred ethoxylated alkyl ether sulfates contain 10 to 6 carbon atoms 5 in the alcohols and in the alkyl groups thereof.
Ethoxylated Cg 18 alkylphenyl ether sulfates containing from 2 to 6 moles of ethylene oxide in the molecule also are suitable for use in the inventive microemulsion compositions. These detergents can be prepared by reacting an alkyl phenol with 2 to 6 moles of ethylene oxide and sulfating and neutralizing the resultant 10 ethoxylated alkylphenol 5 to 20%, and more preferably 10 to 16%, e.g., 13%, and the resulting microemulsion, which will also contain free hydroxyl ions, will be of a pH of at least 12, preferably at least 13, such as in the ranges of 12 to 14 and 13 to 14, e.g.
13.5 or about 14.
The particular combination of Na(AEOS.XEO) surfactant, anionic surfactant, 15 and betaine surfactant, provides a detergent system which coacts with the nonionic surfactant to product a liquid detergent composition with desirable foaming, foam stability and detersive properties. Surprisingly, the resultant homogeneous liquid detergent exhibits the same or better foam performance, both as to initial foam volume and stability ot toam in the presence of soils, and cleaning efficacy as an anionic 20 based light duty liquid detergent (LDLD) as shown in the following Examples.
The essential ingredierits discussed above are solubilized in an aqueous medium comprising water and optionally, solubilizing ingredients such as alcohols and dihydroxy alcohols such as C2-C3 mono- and di-hydoroxy alkanols, e.g. ethanol, isopropanol and propylene glycol. Suitable water soluble hydrotropic salts include 25 sodium, potassium, ammonium and mono-, di- and triethanolammonium salts. While the aqueous medium is primarily water, preferably said solubilizing agents are included in order to control the viscosity of the liquid composition and to control low temperature cloud clear properties. Usually, it is desirable to maintain clarity to a 2~27~
temperature in the range of 5C to 1 0C. Therefore, the proportion of solubilizer generally will be from 0.5% to 8%, preferably 1% to 7%, by weight of the detergent composition with the proportion of ethanol, when present, being 5% of weight or less in order to provide a composition having a flash point above 46C. Preferably the 5 solubilizing ingredient will be propylene glycol. Another extremely effective solubilizing or cosolubilizing agent used at a concentration of 0.1 to 5 wt. percent, more preferably 0.5 to 4.0 weight percent is isethionic acid or an alkali metal salt of isethionic acid having the formula wherein X is hydrogen or an alkali metal cation, preferably sodium.
The foregoing solubilizing ingredients also facilitate the manufacture of the inventive compositions because they tend to inhibit gel formation.
In addition to the previously mentioned essential and optional constituents of 15 the light duty liquid detergent, one may also employ normal and conventional adjuvants, provided they do not adversely affeet the properties of the detergent. Thus, there may be used various coloring agents and perfumes; ultraviolet light absorbers sueh as the Uvinuls, whieh are produets of GAF Corporation; sequèstering agents sueh as ethylene diamine tetraaeetates; magnesium sulfate heptahydrate; pearleseing 20 agents and opaeifiers; pH modifiers; ete. The proportion of sueh adjuvant materials, in total will normally not exeeed 15% of weight of the detergent composition, and the pereentages of most of sueh individual eomponents will be 0.1% to 5% by weight and preferably less than 2% by weight. Sodium formate can be ineluded in the formula as a perservative at a concentration of 0.1 to 4.0%. Sodium bisulfite can be used as a 25 color stabilizer at a concentration of 0.01 to 0.2 wt.%. Typical perservatives are dibromodicyano-butane, citric acid, benzylic alcohol and poly (hexamethylene-biguamide) hydro-chloride and mixtures thereof.
The instant compositions can contain 0 to 5 wt. %, more preferably 1 to 4.0 wt.
% of an alkyl polysaccharide surfactant. The alkyl polysaccharides surfactants, which '~
~, . .. , ,.. ,.. , ~ .. ~.. . . . .......... ... . . .
, 21276~7 are used in conjunction with the aforementioned surfactant have a hydrophobic group containing from 8 to 20 carbon atoms, preferably from 10 to 16 carbon atoms, most preferably from 12 to 14 carbon atoms, and polysaccharide hydrophilic group containing from 1.5 to 10, preferably from 1.5 to 4, most preferably from 1.6 to 2.7 5 saccharide units (e.g., galactoside, glucoside, fructoside, glucosyl, fructosyl; and/or galactosyl units). Mixtures of saccharide moieties may be used in the alkyl polysaccharide surfactants. The number x indicates the number of saccharide units in a particular alkyl polysaccharide surfac~ant. For a particular alkyl polysaccharide molecule x can only assume integral values. In any physical sample of alkyl 10 polysaccharide surfactants there will be in general molecules having different x values. The physical sample can be characterized by the average value of x and this average value can assume non-integral values. In this specification the values of x are to be understood to be average values. The hydrophobic group (R) can be attached at the 2-, 3-, or 4- positions rather than at the 1-position, (thus giving e.g. a 15 glucosyl or galactosyl as opposed to a glucoside or galactoside). However, attachment through the 1- position, i.e., glucosides, galactoside, fructosides, etc., is preferred. In the preferred product the additional saccharide units are predominately attached to the previous saccharide unit's 2-position. Attachment through the 3-, 4-, and 6- positions can also occur. Optionally and less desirably there can be a 20 polyalkoxide chain joining the hydrophobic moiety (R) and the polysaccharide chain.
The preferred alkoxide moiety is ethoxide.
Typical hydrophobic groups include alkyl groups, either saturated or unsaturated, branched or unbranched containing from 8 to 20, preferably from 10 to 18 carbon atoms. Preferably, the alkyl group is a straight chain saturated alkyl group.
25 The alkyl group can contain up to 3 hydroxy groups and/or the polyalkoxide chain can contain up to 30, preferably less than 10, alkoxide moieties.
Suitable alkyl polysaccharides are decyl, dodecyl, tetradecyl, pentadecyl, hexadecyl, and octadecyl, di-, tri-, tetra-, penta-, and hexaglucosides, galactosides, actosides, fructosides, fructosyls, lactosyls, glucosyls and/or galactosyls and mixtures thereof.
The alkyl monosaccharides are relatively less soluble in water than the higher alkyl polysaccharides. When used in admixture with alkyl polysaccharides, the alkyl 5 monosaccharides are solubilized to some extent. The use of alkyl monosaccharides in admixture with alkyl polysaccharides is a preferred mode of carrying out the invention. Suitable mixtures include coconut alkyl, di-, tri-, tetra-, and pentaglucosides and tallow alkyl tetra-, penta-, and hexaglucosides.
The preferred alkyl polysaccharides are alkyl polyglucosides having the 10 formula R2o(cnH2no)r(z)x .'.
wherein Z is derived from glucose, R is a hydrophobic group selected from the group consisting of alkyl, alkylphenyl, hydroxyalkylphenyl, and mixtures thereof in which said alkyl groups contain from 10 to 18, preferably from 12 to 14 carbon atoms; n is 2 or 3 15 preferably 2, r is from 0 to 10, preferable 0; and x is from 1.5 to 8, preferably from 1.5 to 4, most preferably from 1.6 to 2.7. To prepare these compounds a long chain alcohol (R2OH) can be reacted with glucose, in the presence of an acid catalyst to form the desired glucoside. Alternatively the alkyl polyglucosides can be prepared by a two step procedure in which a short chain alcohol (R10H) can be reacted with glucose, in 20 the presence of an acid catalyst to form the desired glucoside. Alternatively the alkyl polyglucosides can be preparèd by a two step procedure in which a short chain alcohol (C1-6) is reacted with glucose or a polyglucoside (x=2 to 4) to yield a short chain alkyl glucoside (x=1 to 4) which can in turn be reacted with a longer chain alcohol (R2OH) to displace the short chain alcohol and obtain the desired alkyl 25 polyglucoside. If this two step procedure is used, the short chain alkylglucosde content of the final alkyl polyglucoside material should be less than 50%, preferably less than 10%, more preferably less than 5%, most preferably 0% of the alkyl polyglucoside.
21276~
The amount of unreacted alcohol (the free fatty alcohol content) in the desired alkyl polysaccharide surfactant is preferably less than 2%, more preferably less than 0.5% by weight of the total of the alkyl polysaccharide. For some uses it is desirable to have the alkyl monosaccharide content less than 10%.
The used herein, "alkyl polysaccharide surfactant" is intended to represent boththe preferred glucose and galactose derived surfactants and the less preferred alkyl polysaccharide surfactants. Throughout this specification, "alkyl polyglucoside" is used to include alkyl polyglycosides because the stereochemistry of the saccharide moiety is changed during the preparation reaction.
An especially preferred APG glycoside surfactant is APG 625 glycoside manufactured by the Henkel Corporation of Ambler, PA. APG25 is a nonionic a!kyl polyglycoside characterized by the formula:
CnH2n+1 0(C6H1 005)XH
wherein n=10 (2%); n=122 (65%); n=14 (21-28%), n=16 (4-8%) and n=18 (0.5%) and x (degree of polymerization) = 1.6. APG 625 has: a pH of 6 to 10 (10% of APG 625 in distilled water); a spedfic gravity at 25C of 1.1 g/ml; a density at 25C of 9.1 Ibs/gallon; a calculated HLB of 12.1 and a Brookfield viscosity at 35C, 21 spindle, 5-10 RPM of 3,000 to 7,000 cps.
The instant compositions can contain a silk derivatives as part of the composition and generally constitute 0.01 to 3.0 % by weight, preferably 0.1 to 3.0%
by weight, most preferably 0.2 to 2.5% by weight of the liquid detergent composition.
Included among the silk derivatives are silk fibers and hydrolyzate of silk fibers.
The silk fibers may be used in the form of powder in preparing the liquid detergent or as a powder of a product obtained by washing and treating the silk fibers with an acid. -25 Preferably, silk fibers are used as a product obtained by hydrolysis with an acid, alkali or enzyme, as disclosed in Yoshiaki Abe et al., U.S. Patent No. 4,839,168; Taichi Watanube et al., U.S. Patent No. 5,009,813; and Marvin E. Goldberg, U.S. Patent No.
Background Of The Invention The present invention relates to novel light duty liquid detergent compositions 5 with high foaming properties, containing a nonionic surfactant, a specific group of anionic surfactants, and a Zwitterionic betaine surfactant wherein the surfactants are dissolved in an aqueous medium.
Nonionic surfactants are in general chemically inert and stable toward pH
change and are therefore well suited for mixing and formulation with other matarials.
10 The superior performance of nonionic surfactants on the removal of oily soil is well recognized. Nonionic surfactants are also known to be mild to human skin. However, as a class, nonionic surfactants are known to be low or moderate foamers.
Consequently, for detergents which require copious and stable foam, the application of nonionic surfactants is limited. There have been substantial interest and efforts to 15 develop a high foaming detergent with nonionic surfactants as the major ingredient.
Little has been achieved.
The prior art is replete with light duty liquid detergent compositions containin~
nonionic surfactants in combination with anionic andlor betaine surfactants wherein the nonionic detergent is not the major active surfactant, as shown in U.S. Patent No.
20 3,S58,985 wherein an anionic based shampoo contains a minor amount of a fatty acid alkanolamide U.S. Patent No. 3,769,398 discloses a betaine-based shampoo containing minor amounts of nonionic surfactants. This patent states that the low foaming properties of nonionic detergents renders its use in shampoo compositions non-preferred. U.S. Patent No. 4,329,335 also discloses a shampoo containing a 25 betaine surfactant as the major ingredient and minor amounts of a nonionic surfactant and of a fatty acid mono- or di-ethanolamide. U.S. Patent No. 4,259,204 discloses a shampoo comprising 0.8-20% by weight of an anionic phosphoric acid ester and oneadditional surfactant which may be either anionic, amphoteric, or nonionic. U.S.Patent No. 4,329,334 discloses an anionic-amphoteric based shampoo containing a .,.. , .: :,. :. :.: . , i. - . - , . . . , -F-:; . ~
- 21276~7 major amount of anionic surfactant and lesser amounts of a betaine and nonionic surfactants.
U.S. Patent No. 3,935,129 discloses a liquid cleaning composition based on the alkali metal silicate content and containing five basic ingredients, namely, urea, 5 glycerin, triethanolamine, an anionic detergent and a nonionic detergent. The silicate content determines the amount of anionic and/or nonionic detergent in the liquidcleaning composition. However~ the foaming property of these detergent composifions is not discussed therein.
U.S. Patent No. 4,129,515 discloses a heavy duty liquid detergent for 10 laundering fabrics comprising a mixture of substantially equal amounts of anionic and nonionic surfactants, alkanolamines and magnesium salts, and, optionally, zwitterionic surfactants as suds modifiers.
U.S. Patent No. 4,224,195 discloses an aqueous detergent composition for laundering socks or stockings comprising a specific group of nonionic detergents, 15 namely, an ethylene oxide of a secondary alcohol, a specific group of anionicdetergents, namely, a sulfuric ester salt of an ethylene oxide adduct of a secondary alcohol, and an amphoteric surfactant which may be a betaine, wherein either theanionic or nonionic surfactant may be the major ingredient.
The prior art also discloses detergent compositions containing all nonionic 20 surfactants as shown in U.S. Patent Nos. 4,154,706 and 4,329,336 wherein the shampoo compositions contairi a plurality of particular nonionic surtactants in order to effect desirable foaming and detersive properties despite the fact that nonionicsurfactants are usually deficient in such properties.
U.S. Patent No. 4,013,787 discloses a piperazine based polymer in 25 conditioning and shampoo cornpositions which may contain all nonionic surtactant or all anionic surtactant.
U.S. Patent No. 4,450,091 discloses high viscosity shampoo compositions containing a blend ot an amphoteric betaine surtactant, a 21276~7 62301-1~74 polyoxybutylenepolyoxyethylene nonionic detergent, an anionlc surfactant, a fatty acid alkanolamide and a polyoxyalkylene glycol fatty ester.
United States Patent No. 4,595,526 describes a composition comprising a nonionic surfactant, a betaine surfactant, an anionic surfactant and a C12-C14 fatty acid monoethanolamide foam stabllizer.
However, none of the above-cited patents discloses a hlgh foaming, nonlonic based, liquid detergent composition containing a nonionic surfactant, a supplementary high foaming ethoxylated alkyl ether sulfate anionic surfactant and a supplementary foaming zwitterionic surfactant selected from betaine type surfactants as the three essential ingredients wherein the composition does not contain any amine oxide, calcium carbonate, polymeric or clay thickeners, abrasive, clays, silicas, -~
alkyl glycine surfactant, cyclic imidinium surfactant, or more than 3.0 wt.% of a fatty acld or a metal salt of the fatty acid compounds.
None of the above-cited patents discloses a high -~
foaming, nonionic based, liquid detergent composition containing a - nonionic surfactant as a major active ingredient and lesæer amounts of a magnesium salt of C8-C18 ethoxylated alkyl ether sulfate surfactant, an alkali metal salt of an alkyl sulfate surfactant, and a supplementary foaming zwitterlonic surfactant selected from betalne type surfactants as the four essential ingredients, wherein the nonionic ingredient constitutes more than 50% of the total surfactant content. ;~
2127~.57 Summarv Of The Invention It has now been found that a high foaming liquid detergent can be formulated with a nonionic surfactant which has desirable cleaning properties, mildness to the human skin.
A major object of this invention is to provide a novel, liquid detergent wlth desirable high foaming and cleaning properties which is mlld to the human skln.
Additional ob~ects, advantages and novel features of the invention will be set forth in part in the description which follows, and in part will become apparent to those skilled in the art upon examination of the following or may be learned by practice of the invention. The objects and advantages of ~he invention may be realized and attained by means of the lnstrumentalities and combinations particularly pointed out in the appended claims.
To achieve the foregoing and other objects and in accordance with the purpose of ~he present inventlon, as embodled and broadly described hereln the novel, high foamlng, llght duty llquld detergent of this invention comprises three essential surfactantæ: a water soluble, ethoxylated, nonionic surfactant; a foaming water soluble zwitterionic surfactant selected from the class of betaines; and an ethoxylated alkyl ether sulfate surfactant, wherein the ingredients are dissolved in an aqueous vehicle, and the composition does not contain any amine oxide, alkanolamlde ingredients.
More specifically, the present invention relates to a high foaming, nonionic based, liquid detergent comprising a 2127~
nonlonic surfactant selected from the group consistlng of water soluble primary aliphatic alcohol ethoxylates, secondary allphatic alcohol ethoxylates, alkyl phenol ethoxylates and alcohol ethylene oxide/propylene oxide condensates; a water soluble zwitterionic betaine surfactant; an ethoxylated alkyl ether sulfate surfactant;
and optionally a C8-C14 alkyl sulfate surfactant wherein the lngredlents are dissolved in an aqueous vehicle.
The total amount of surfactants may constitute 10%-55%, preferably 20% - 40%, most preferably 25%-35%, by weight of the liquid composition.
In a first embodiment, the liquid aqueous detergent compositlon of the present invention contains a nonionic surfactant, an ethoxylated alkyl (ether) sulfate anionic surfactant, and a zwitterionic betalne surfactant, and does not contain amine oxides, alkali metal or alkallne earth metal carbonates, polymerlc or clay thickeners, clays, abrasives, alkyl glycine surfactants, cyclic imldinium surfactants, sillcas or more than 3 wt.% of a fatty acid or a metal salt of a fatty acid.
In a second embodiment, the nonionic based, liquid detergent composition of the present invention contains a major amount of the nonionic surfactant supplemented with lesser amounts of a magnesium salt of the ethoxylated alkyl ether sulfate surfactant, a sodium salt of the alkyl sulfate surfactant, and the ~-zwitterionic betalne surfactant, wherein the composltlon does not contain any amine oxlde, fatty acld alkanolamides, clay, silica, abrasive, clay or polymeric thickeners, alkali metal or alkaline earth metal carbonate or more than 3 wt.% of a fatty acid or its , "
s . ,:
2127~57 metal salt.
Detailed DescriPtion Of The Invention In the first embodiment, the high foaming nonionic based light duty liquid detergent composition of the instant invention comprises approximately by weight: 10 to 25 wt.~ of a water soluble nonionic surfactant; 8 to 16 wt.~ of an ethoxylated alkyl ether sulfate; and 2 to 12 wt.% of a betaine surfactant; and the balance (e.g. 47 to 80 wt.%) of water, wherein the composition does not contain any amine oxides, alkali metal or alkaline earth metal carbonates (e.g., calcium carbonate), polymeric or clay thickeners, abrasives, clays, silicas, alkyl glycine surfactants, cyclic imidinium surfactants, or more than 3 wt.% of a fatty acid or a metal salt of the fatty acid.
In the second embodiment, the liquid detergent compositions of the present invention comprises approximately by weight, 10 to 20 wt.%, more preferably 11 to 17 wt.% of a nonlonlc surfactant; 0.5 to 8 wt.% more preferably 1 to 7 wt.% of an alkali metal or ammonium salt of a C8-C14 alkyl sulfate surfactant; 0.5 to 8 wt.% more preferably 1 to 7 wt.% of a -magnesium salt of a C8-C18 ethoxylated alkyl ether sulfate surfactant and 2 to 10 wt.%, more preferably 3 to 9 wt.% of a betaine zwitterionic surfactant, wherein the composition does not contain any amide oxides, fatty acid alkanolamides, alkali metal or alkaline earth metal carbonates, clays, silicaæ, abrasives, clay or polymeric thickeners or more than 3 wt.% of fatty acids or their metals salts.
The nonionic surfactant which constitutes the major ~ 21276~7 ingredient in the liquid detergent composition iæ present ln amounts of 10 to 25%, preferably 15 to 20% by welght of the composition and provides superior performance in the removal of oily soil and mildness to human skln.
5b 2 1 2 7 6 ~ l The water soluble nonionic surfactants utilized in this invention are commercially well known and include the primary aliphatic alcohol ethoxylates, secondary aliphatic alcohol ethoxylates, alkylphenol ethoxylates and ethylene-oxide-propylene oxide condensates on primary alkanols, such a Plurafacs (BASF) and 5 condensates of ethylene oxide with sorbitan fatty acid esters such as the Tweens (ICI).
The nonionic synthetic organic detergents generally are the condensation products of an organic aliphatic or alkyl aromatic hydrophobic compound and hydrophilic ethylene oxide groups. Practically any hydrophobic compound having a carboxy, hydroxy, amido, or amino group with a free hydrogen attached to the nitrogen can be 10 condensed with ethylene oxide or with the polyhydration product thereof, polyethylene glycol, to form a water soluble nonionic detergent. Further, the length of the polyethenoxy hydrophobic and hydrophilic elements.
The nonionic detergent class includes the condensation products of a higher alcohol (e.g., an alkanol containing 8 to 18 carbon atoms in a straight or branched 15 chain configuration) condensed with 5 to 30 moles of ethylene oxide, for example, lauryl or myristyl alcohol condensed with 16 moles of ethylene oxide (EO), tridecanol condensed with 6 to moles of EO, myristyl alcohol condensed with 10 moles of EO per mole ot myristyl alcohol, the condensation product of EO with a cut of coconut fatty alcohol containing a mixture of fatty alcohols with alkyl chains varying from 10 to 14 20 carbon atoms in length and wherein the condensate contains either 6 moles of EO per mole of total alcohol or 9 moles of EO per mole of alcohol and tallow alcohol ethoxylates containing 6 EO to 11 EO per mole of alcohol.
A preferred group of the foregoing nonionic surfactants are the Neodol ethoxylates (Shell Co.), which are higher aliphatic, primary alcohol containing 9-15 25 carbon atoms, such as Cg-C1 1 alkanol condensed with 8 moles of ethylene oxide (Neodol 91-8), C12 13 alkanol condensed with 6.5 moles ethylene oxide (Neodol 23-6.5), C12 15 alkanol condensed with 12 moles ethylene oxide (Neodol 25-12), C14 15 alkanol condensed with 13 moles ethylene oxide (Neodol 45-13), and the like.
21276~7 Such ethoxamers have an HLB (hydrophobic lipophiiic balance) value of 8 to 15 and give good OAN emulsification, whereas ethoxamers with HLB values below 8 containless than ~ ethyleneoxide groups and tend to be poor emulsifiers and poor detergents.
Additional satisfactory water soluble alcohol ethylene oxide condensates are the condensation products of a secondary aliphatic alcohol containing 8 to 18 carbon atoms in a straight or branched chain configuration condensed with 5 to 30 moles of ethylene oxide. Examples of commercially available nonionic detergents of the foregoing type are C1 1-C15 secondary alkanol condensed with either 9 EO (Tergitol 15-S-9) or 12 EO (Tergitol 15-S-12) marketed by Union Carbide.
Other suitable nonionic detergents include the polyethylene oxide condensates of one mole of alkyl phenol containing from 8 to 18 carbon atoms in a straight- or branched chain alkyl group with 5 to 30 moles of ethylene oxide. Specific examples of alkyl phenol ethoxylates include nonyl condensed with 9.5 moles of EO per mole of nonyl phenol, dinonyl phenol condensed with 12 moles of EO per mole of dinonyl phenol, dinonyl phenol condensed with 15 moles of EO per mole of phenol and di- -isoc~ylphenol condensed with 15 moles of EO per mole of phenol. Commercially available nonionic surfactants of this type include Igepal C0-630 (nonyl phenol ethoxylate) marketed by GAF Corporation.
Condensates of 2 to 30 moles of ethylene oxide with sorbitan mono- and tri-C10-C20 all~anoic acid esters having a I~LB of 8 to 15 also may be employed as the nonionic detergent ingredient in the described shampoo. These surfactants are well known and are available from Imperial Chemical Industries under the Tween trade name. Suitable surfactants include polyoxyethylene (4) sorbitan monolaurate, polyoxyethylene (4) sorbitan monostearate, polyoxyethylene (20) sorbitan trioleate and polyoxyethylene (20) sorbitan tristearate.
The water-solubie zwitterionic surfactant, which is also an essential ingredientof present liquid detergent composition, constitutes 2 to 12%, preferably 3 to 10%, by 2~27 ~ra7 weight and provides good foaming properties and mildness to the present liquid detergent. The zwitterionic surfactant is a water soluble betaine having the general formula:
R1 - N - R4 - CO~
wherein R1 is an alkyl group having 10 to 20 carbon atoms, preferably 12 to 16 carbon atoms, or the amido radical:
O H
Il I
R-C - N - (CH2)a~
wherein R is an alkyl group having 9 to 19 carbon atoms and a is the integer 1 to 4; R2 and R3 are each alkyl groups having 1 to 3 carbons and preferably 1 carbon; R4 is an alkylene or hydroxyalkylene group having from 1 to 4 carbon atoms and, optionally, one hydroxyl group. Typical alkyldimethyl betaines include decyl dimethyl betaine or 2-(N-decyl-N, N-dimethyl-ammonia) acetate, coco dimethyl betaine or 2-(N-coco N, N-dimethylammonio) acetate, myristyl dimethyl betaine, palmityl dimethyl betaine, lauryl dimethyl betaine, cetyl dimethyl betaine, stearyl dimethyl betaine, eto. The amidobetaines similarly include cocoamidoethylbetaine, cocoamidopropyl betaine and the like. A preferred betaine is coco (Cg-C1g) amidopropyldimethyl betaine.
The anionic sulfate and sulfonate surfactants which may be used in the detergent of ~his invention are water soluble such as triethanolamine and include the sodium, potassium, ammonium and ethanolammonium salts of Cg-C1g alkyl sulfates such as lauryl sulfate, myristyl sulfate and the like; linear Cg-C16 alkyl benzene sulfonates; C1 o-C20 paraffin sulfonates and alpha olefin sulfonates containing about 10-24 carbon atoms. The preferred sulfate surfactant is a Cg to C14 sulfate and is present in the composition at a concentration of about 0.5 to 8 wt. %.
The paraffin sulfonates may be monosulfonates or di-sulfonates and usually are mixtures thereof, obtained by sulfonating paraffins of 10 to 20 carbon atoms.
2127~7 Preferred paraffin sulfonates are those of C12-1 g carbon atoms chains, and morepreferably they are of C14 17 chains. Paraffin sulfonates that have the sulfonate group(s) distributed along the paraffin chain are described in U.S. Patents 2,503,280; 2,507,088; 3,260,744; and 3,372,188; and also in German Patent 735,096. Such compounds may be made to specifications and desirably the content of paraffin sulfonates outside the C14 17 range will be minor and will be minimized, as will be any contents of di- or poly-sulfonates.
Examples of suitable other sulfonated anionic detergents are the well known higher alkyl mononuclear aromatic sulfonates, such as the higher alkylbenzene sulfonates containing 9 to 18 or preferably 9 to 10 to 15 or 16 carbon atoms in the higher alkyl group in a straight or branched chain, or Cg 1s alkyl toulene sulfonates.
A preferred alkylbenzene sulfonate is a linear alkylbenzene sulfonate having a higher content of 3-phenyl (or higher) isomers and a correspondingly lower content (well below 50%) of 2-phenyl (or lower) isomers, such as those sulfonates wherein the benzene ring is attached mostly at the 3 or higher (for example 4, 5, 6 or 7) position of the alkyl group and the content of the isomers in which the benzene ring is attached in the 2 or 1 position is correspondingly low. Preterred materials are set forth in U.S.
Patent 3,320,174, especially those in which the alkyls are of 10 to 13 carbon atoms.
The ethoxylated alkyl ether sulfate (AEOS.xEO) is depicted by the formula: R-(OCHCHC2)x OSO3M wherein x is about I to 22, more preferably about 1 to about 10and R is an alkyl group having about 8 to 18 carbon atoms and more preferably about 12 to about 15 carbon atoms and natural cuts for example C12-1 4. C12-C1 3 and C1 2-15 and M is an alkali earth metal cation such as magnesium. Examples of satisfactory anionic ethoxylated sulfate are the Cg 18 ethoxylated alkyl ether sulfate salts having the formula: R~(ocH2-H4)n OSO3M wherein R' is alkyl of 8 or 9 to 18carbon atoms, n is 1 to 22, preferably 1 to 5, and M is a magnesium cation. The ethoxylated alkyl ether sulfates may be made by sulfating the condensation product of 21276~7 ethylene oxide and Cg 1 8 alkanol, and neutralizing the resultant product. The ethoxylated alkyl ether sulfates differ from one another in the number of carbon atoms in the alcohols and in the number of moles of ethylene oxide reacted with one mole of such alcohol. Preferred ethoxylated alkyl ether sulfates contain 10 to 6 carbon atoms 5 in the alcohols and in the alkyl groups thereof.
Ethoxylated Cg 18 alkylphenyl ether sulfates containing from 2 to 6 moles of ethylene oxide in the molecule also are suitable for use in the inventive microemulsion compositions. These detergents can be prepared by reacting an alkyl phenol with 2 to 6 moles of ethylene oxide and sulfating and neutralizing the resultant 10 ethoxylated alkylphenol 5 to 20%, and more preferably 10 to 16%, e.g., 13%, and the resulting microemulsion, which will also contain free hydroxyl ions, will be of a pH of at least 12, preferably at least 13, such as in the ranges of 12 to 14 and 13 to 14, e.g.
13.5 or about 14.
The particular combination of Na(AEOS.XEO) surfactant, anionic surfactant, 15 and betaine surfactant, provides a detergent system which coacts with the nonionic surfactant to product a liquid detergent composition with desirable foaming, foam stability and detersive properties. Surprisingly, the resultant homogeneous liquid detergent exhibits the same or better foam performance, both as to initial foam volume and stability ot toam in the presence of soils, and cleaning efficacy as an anionic 20 based light duty liquid detergent (LDLD) as shown in the following Examples.
The essential ingredierits discussed above are solubilized in an aqueous medium comprising water and optionally, solubilizing ingredients such as alcohols and dihydroxy alcohols such as C2-C3 mono- and di-hydoroxy alkanols, e.g. ethanol, isopropanol and propylene glycol. Suitable water soluble hydrotropic salts include 25 sodium, potassium, ammonium and mono-, di- and triethanolammonium salts. While the aqueous medium is primarily water, preferably said solubilizing agents are included in order to control the viscosity of the liquid composition and to control low temperature cloud clear properties. Usually, it is desirable to maintain clarity to a 2~27~
temperature in the range of 5C to 1 0C. Therefore, the proportion of solubilizer generally will be from 0.5% to 8%, preferably 1% to 7%, by weight of the detergent composition with the proportion of ethanol, when present, being 5% of weight or less in order to provide a composition having a flash point above 46C. Preferably the 5 solubilizing ingredient will be propylene glycol. Another extremely effective solubilizing or cosolubilizing agent used at a concentration of 0.1 to 5 wt. percent, more preferably 0.5 to 4.0 weight percent is isethionic acid or an alkali metal salt of isethionic acid having the formula wherein X is hydrogen or an alkali metal cation, preferably sodium.
The foregoing solubilizing ingredients also facilitate the manufacture of the inventive compositions because they tend to inhibit gel formation.
In addition to the previously mentioned essential and optional constituents of 15 the light duty liquid detergent, one may also employ normal and conventional adjuvants, provided they do not adversely affeet the properties of the detergent. Thus, there may be used various coloring agents and perfumes; ultraviolet light absorbers sueh as the Uvinuls, whieh are produets of GAF Corporation; sequèstering agents sueh as ethylene diamine tetraaeetates; magnesium sulfate heptahydrate; pearleseing 20 agents and opaeifiers; pH modifiers; ete. The proportion of sueh adjuvant materials, in total will normally not exeeed 15% of weight of the detergent composition, and the pereentages of most of sueh individual eomponents will be 0.1% to 5% by weight and preferably less than 2% by weight. Sodium formate can be ineluded in the formula as a perservative at a concentration of 0.1 to 4.0%. Sodium bisulfite can be used as a 25 color stabilizer at a concentration of 0.01 to 0.2 wt.%. Typical perservatives are dibromodicyano-butane, citric acid, benzylic alcohol and poly (hexamethylene-biguamide) hydro-chloride and mixtures thereof.
The instant compositions can contain 0 to 5 wt. %, more preferably 1 to 4.0 wt.
% of an alkyl polysaccharide surfactant. The alkyl polysaccharides surfactants, which '~
~, . .. , ,.. ,.. , ~ .. ~.. . . . .......... ... . . .
, 21276~7 are used in conjunction with the aforementioned surfactant have a hydrophobic group containing from 8 to 20 carbon atoms, preferably from 10 to 16 carbon atoms, most preferably from 12 to 14 carbon atoms, and polysaccharide hydrophilic group containing from 1.5 to 10, preferably from 1.5 to 4, most preferably from 1.6 to 2.7 5 saccharide units (e.g., galactoside, glucoside, fructoside, glucosyl, fructosyl; and/or galactosyl units). Mixtures of saccharide moieties may be used in the alkyl polysaccharide surfactants. The number x indicates the number of saccharide units in a particular alkyl polysaccharide surfac~ant. For a particular alkyl polysaccharide molecule x can only assume integral values. In any physical sample of alkyl 10 polysaccharide surfactants there will be in general molecules having different x values. The physical sample can be characterized by the average value of x and this average value can assume non-integral values. In this specification the values of x are to be understood to be average values. The hydrophobic group (R) can be attached at the 2-, 3-, or 4- positions rather than at the 1-position, (thus giving e.g. a 15 glucosyl or galactosyl as opposed to a glucoside or galactoside). However, attachment through the 1- position, i.e., glucosides, galactoside, fructosides, etc., is preferred. In the preferred product the additional saccharide units are predominately attached to the previous saccharide unit's 2-position. Attachment through the 3-, 4-, and 6- positions can also occur. Optionally and less desirably there can be a 20 polyalkoxide chain joining the hydrophobic moiety (R) and the polysaccharide chain.
The preferred alkoxide moiety is ethoxide.
Typical hydrophobic groups include alkyl groups, either saturated or unsaturated, branched or unbranched containing from 8 to 20, preferably from 10 to 18 carbon atoms. Preferably, the alkyl group is a straight chain saturated alkyl group.
25 The alkyl group can contain up to 3 hydroxy groups and/or the polyalkoxide chain can contain up to 30, preferably less than 10, alkoxide moieties.
Suitable alkyl polysaccharides are decyl, dodecyl, tetradecyl, pentadecyl, hexadecyl, and octadecyl, di-, tri-, tetra-, penta-, and hexaglucosides, galactosides, actosides, fructosides, fructosyls, lactosyls, glucosyls and/or galactosyls and mixtures thereof.
The alkyl monosaccharides are relatively less soluble in water than the higher alkyl polysaccharides. When used in admixture with alkyl polysaccharides, the alkyl 5 monosaccharides are solubilized to some extent. The use of alkyl monosaccharides in admixture with alkyl polysaccharides is a preferred mode of carrying out the invention. Suitable mixtures include coconut alkyl, di-, tri-, tetra-, and pentaglucosides and tallow alkyl tetra-, penta-, and hexaglucosides.
The preferred alkyl polysaccharides are alkyl polyglucosides having the 10 formula R2o(cnH2no)r(z)x .'.
wherein Z is derived from glucose, R is a hydrophobic group selected from the group consisting of alkyl, alkylphenyl, hydroxyalkylphenyl, and mixtures thereof in which said alkyl groups contain from 10 to 18, preferably from 12 to 14 carbon atoms; n is 2 or 3 15 preferably 2, r is from 0 to 10, preferable 0; and x is from 1.5 to 8, preferably from 1.5 to 4, most preferably from 1.6 to 2.7. To prepare these compounds a long chain alcohol (R2OH) can be reacted with glucose, in the presence of an acid catalyst to form the desired glucoside. Alternatively the alkyl polyglucosides can be prepared by a two step procedure in which a short chain alcohol (R10H) can be reacted with glucose, in 20 the presence of an acid catalyst to form the desired glucoside. Alternatively the alkyl polyglucosides can be preparèd by a two step procedure in which a short chain alcohol (C1-6) is reacted with glucose or a polyglucoside (x=2 to 4) to yield a short chain alkyl glucoside (x=1 to 4) which can in turn be reacted with a longer chain alcohol (R2OH) to displace the short chain alcohol and obtain the desired alkyl 25 polyglucoside. If this two step procedure is used, the short chain alkylglucosde content of the final alkyl polyglucoside material should be less than 50%, preferably less than 10%, more preferably less than 5%, most preferably 0% of the alkyl polyglucoside.
21276~
The amount of unreacted alcohol (the free fatty alcohol content) in the desired alkyl polysaccharide surfactant is preferably less than 2%, more preferably less than 0.5% by weight of the total of the alkyl polysaccharide. For some uses it is desirable to have the alkyl monosaccharide content less than 10%.
The used herein, "alkyl polysaccharide surfactant" is intended to represent boththe preferred glucose and galactose derived surfactants and the less preferred alkyl polysaccharide surfactants. Throughout this specification, "alkyl polyglucoside" is used to include alkyl polyglycosides because the stereochemistry of the saccharide moiety is changed during the preparation reaction.
An especially preferred APG glycoside surfactant is APG 625 glycoside manufactured by the Henkel Corporation of Ambler, PA. APG25 is a nonionic a!kyl polyglycoside characterized by the formula:
CnH2n+1 0(C6H1 005)XH
wherein n=10 (2%); n=122 (65%); n=14 (21-28%), n=16 (4-8%) and n=18 (0.5%) and x (degree of polymerization) = 1.6. APG 625 has: a pH of 6 to 10 (10% of APG 625 in distilled water); a spedfic gravity at 25C of 1.1 g/ml; a density at 25C of 9.1 Ibs/gallon; a calculated HLB of 12.1 and a Brookfield viscosity at 35C, 21 spindle, 5-10 RPM of 3,000 to 7,000 cps.
The instant compositions can contain a silk derivatives as part of the composition and generally constitute 0.01 to 3.0 % by weight, preferably 0.1 to 3.0%
by weight, most preferably 0.2 to 2.5% by weight of the liquid detergent composition.
Included among the silk derivatives are silk fibers and hydrolyzate of silk fibers.
The silk fibers may be used in the form of powder in preparing the liquid detergent or as a powder of a product obtained by washing and treating the silk fibers with an acid. -25 Preferably, silk fibers are used as a product obtained by hydrolysis with an acid, alkali or enzyme, as disclosed in Yoshiaki Abe et al., U.S. Patent No. 4,839,168; Taichi Watanube et al., U.S. Patent No. 5,009,813; and Marvin E. Goldberg, U.S. Patent No.
5,069,898, each incorporated herein by reference.
.
2127 ~7 Another silk derivative which may be employed in the composition of the present invention is protein obtained from degumming raw silk, as disclosed, forexample, in Udo Hoppe et al., U.S. Patent No. 4,839,165, incorporated herein by reference. The principal protein obtained from the raw silk is sericin which has an 5 empirical formula of C1sH2sO3Ns and a molecular weight of 323.5.
Another example of a silk derivative for use in the liquid detergent compositionof the present invention is a fine powder of silk fibroin in nonfibrous or particulate form, as disclosed in Kiyoshi Otoi et al., U.S. Patent No. 4,233,212, incorporated herein by reference.
The fine powder is produced by dissolving a degummed silk material in at least one solvent selected from, for example, an aqueous cupriethylene diamine solution, an aqueous ammoniacal solution of cupric hydroxide, an aqueous alkaline solution of cupric hydroxide and glycerol, an aqueous lithium bromide solution, an aqueous solution of the chloride, nitrate or thiocyanate of calcium, magnesium or zinc and an aqueous sodium thiocyanate solution. The resulting fibroin solution is then dialyzed.
The dialyzed aqueous silk fibroin solution, having a silk fibroin concentration of from 3 to 20% by weight, is subjected to at least one treatment for coagulating and precipitating the silk fibroin, such as, for example, by the addition of a coagulating salt, by aeration, by coagulation at the isoelectric point, by exposure to ultrasonic waves, by agitation at high shear rate and the like. ~ ;
The resulting product is a silk fibroin gel which may be incorporated directly into the liquid detergent composition or the same may be dehydrated and dried into a powder and then dissolved in the liquid detergent composition.
The silk material which may be used to form the silk fibroin includes cocoons, raw silk, waste cocoons, raw silk waste, silk fabric waste and the like. The silk material is degummed or freed from sericin by a conventional procedure such as, for example, by washing in warm water containing a surfact-active agent or an enzyme, and then dried. The degummed material is dissolved in the solvent and preheated to a :`: :
2~27g~,7 [emperature of from 60 to 95C, preferably 70 to 85C. Further details of the process of obtaining the silk fibroin are discussed in U.S. Patent No. 4,233,212.
A preferred silk derivative is a mixture of two or more individual amino acids which naturally occur in silk. The principal silk amino acids are glycine, alanine, 5 serine and tyrosine.
A silk amino acid mixture resulting from the hydrolysis of silk of low molecularweight and having a specific gravity of at least 1 is produced by Croda, Inc. and sold under the trade name "CROSILK LIQUID" which typically has a solids content in the range of 27 to 31% by weight. Further details of the silk amino acid mixture can be 10 found in Wendy W. Kim et al., U.S. Patent No. 4,906,460, incorporated herein by reference. A typical amino acid composition of "CROSILK LIQUID" is shown in the following Table .
AMINO ACIDPERCENT BY WEiGHT
Alanine 28.4 Givcine 2.0 Leucine 1.2 i~roline 1.2 Tvrosine o 6 i henvlalanine o g Serlne 1 s.4 Ar~inine -- _ 1 s As~arlic Acki 4 7 Gu~c AcW 4;1 Isoleucine o.s _ H~sticiine o. a Cvstine 01 Methionine 0 2 TOTAL 99.9 The instant compositions can contain a viscosity modifying solvent at a concentration of 0.1 to 5.0 weight percent, more preferably 0.5 to 4.0 weight percent.
The viscosity modifying agent is an alcohol of the formula 2127~ )7 wherein R1 = CH3, CH2CH3 R2 = CH3, CH2CH3 R3 = CH2OH, CH2CH2OH;
which is preferably 3-methyl-3-methoxy-butanol.
The 3-methyl-3-methoxy butanol is commercially avaiiable from Sattva Chemical Company of Stamford, Connecticut and Kuraray Co., Ltd., Osaka, Japan.
The instant composition can contain 0.1 to 4.0% of a protein selected from the group consisting of hydrolyzed animal collagen protein obtained by an enzymatic hydrolysis, lexeine protein, vegetal protein and hydrolyzed wheat protein and mixtures thereof.
The present light duty liquid detergents such as dishwashing liquids are readilymade by simple mixing methods from readily available components which, on storage, do not adversely affect the entire composition. However, it is preferred that the nonionic surfactant be mixed with the solubilizing ingredients, e.g., ethanol and, if present, prior to the addition of the water to prevent possible gelation. The nonionic based surfactant system is prepared by sequentially adding with agitation the anionic surfactant and the betaine to the nonionic surfactant, cosolubilizing agent and water, and then adding with agitation the formula amount of water to form an aqueous solution of the surfactant system. The use of mild heating (up to 1 00C.) assists in the solubilization of the surfactants. The viscosities are adjustable by changing the total percentage of active ingredienfs. No polymeric or clay thickening agent is added. In all such cases the product made will be pourable from a relatively narrow mouth bottle (1.5 cm. diameter) or opening, and the viscosity of the detergent formulation will not be so low as to be like water. The viscosity of the detergent desirably will be at least 100 centipoises (cps) at room temperature, but may be up to 1,000 centipoises as measured with a Brookfield Viscometer using a number 3 spindle rotating at 18 rpms.
Its viscosity may approximate those of cbmmercially acceptable detergents now on the market. The detergent viscosity and the detergent itself remain stable on storage for ,7,.. : ''' ' ''''' i :' ' ''"' ~ ' ' ' ' 2127~
,engthy periods of time, without color changes or ~ettling out of any insoluble materials. The pH of this formation is substantially neutral to skin, e.g., 4.5 to 8 and preferably 5 to 5.5. The compositions of the instant invention are optically clear - that is they exhibit a light transmission of at least 95%, more preferably at least 98%.
These products have unexpectedly desirably properties. For example, the foam quality and detersive property is equal to or better than standard light duty liquid detergents while using a nonionic surfactant as the primary surfactant and minimal amounts of anionic surfactant, thereby achieving a mild, non-irritating liquid detergent.
The following examples are merely illustrative of the invention and are not to be construed as limiting thereof.
E)(AMPLE 1 The following formulas were prepared at room temperature by simple liquid mixing procedures as previously described.
A B C
NEC~DOL 14 15.5 12.5 14.5 9~e~L~_ 7 5.5 ~--- 7 Na (AEOS.1~--11 5 10 5 10 5 Sod~ 3 0.05 0.05 0.03 Perfume 0.2 0.2 0.2 -~
Water Balance Balance Balance Mono ethanol amide 0 1 5 .
3.1 31 3 5 HEDT ~ 0.08 0.08 0 08 SheU Foam 2.0 2.0 2.0 S ~~
Brookfield viscosity~VTD~i~;~ 410 350 428 spindle, 18 rpms (cps) The Shell Foam and Shake Foam Height test were run against a control sample of a commercial Palmolive Skin Sensitive formulation manufactured by 20 Colgate-Palmolive Co. The designation "s" means that the sample being tested has the same value as the commercial sample. The designation "-" means that the value obtained is less than the value obtained for the commercial sample. The designation 2127 ~7 "+" means that the value obtained is superior to the value obtained for the commercial sample.
The following formula was prepared at room temperature by simple liquid mixing 5 procedures as previously described A
Nonionic Neodol 1-7 14.5 Elfan NS248 SMG (28% Al) 17.86 AEOSE08:1 Magnesium Salt Sodium lauryl sulfate (28%) 17 Cocoamido propyl betaine 16.67 30% Betadet HR-S(KAO) Vencol (progiven) 1.5 EDTA 0.1 Sodium formate 2.0 Sodium bisulfite 0.05 Perfume 0.2 Water Balance Appearance 5.0 : ~ -Brookfield vfscosity, RT #30 spindle, ~ 60~0 10 rpm (cps)
.
2127 ~7 Another silk derivative which may be employed in the composition of the present invention is protein obtained from degumming raw silk, as disclosed, forexample, in Udo Hoppe et al., U.S. Patent No. 4,839,165, incorporated herein by reference. The principal protein obtained from the raw silk is sericin which has an 5 empirical formula of C1sH2sO3Ns and a molecular weight of 323.5.
Another example of a silk derivative for use in the liquid detergent compositionof the present invention is a fine powder of silk fibroin in nonfibrous or particulate form, as disclosed in Kiyoshi Otoi et al., U.S. Patent No. 4,233,212, incorporated herein by reference.
The fine powder is produced by dissolving a degummed silk material in at least one solvent selected from, for example, an aqueous cupriethylene diamine solution, an aqueous ammoniacal solution of cupric hydroxide, an aqueous alkaline solution of cupric hydroxide and glycerol, an aqueous lithium bromide solution, an aqueous solution of the chloride, nitrate or thiocyanate of calcium, magnesium or zinc and an aqueous sodium thiocyanate solution. The resulting fibroin solution is then dialyzed.
The dialyzed aqueous silk fibroin solution, having a silk fibroin concentration of from 3 to 20% by weight, is subjected to at least one treatment for coagulating and precipitating the silk fibroin, such as, for example, by the addition of a coagulating salt, by aeration, by coagulation at the isoelectric point, by exposure to ultrasonic waves, by agitation at high shear rate and the like. ~ ;
The resulting product is a silk fibroin gel which may be incorporated directly into the liquid detergent composition or the same may be dehydrated and dried into a powder and then dissolved in the liquid detergent composition.
The silk material which may be used to form the silk fibroin includes cocoons, raw silk, waste cocoons, raw silk waste, silk fabric waste and the like. The silk material is degummed or freed from sericin by a conventional procedure such as, for example, by washing in warm water containing a surfact-active agent or an enzyme, and then dried. The degummed material is dissolved in the solvent and preheated to a :`: :
2~27g~,7 [emperature of from 60 to 95C, preferably 70 to 85C. Further details of the process of obtaining the silk fibroin are discussed in U.S. Patent No. 4,233,212.
A preferred silk derivative is a mixture of two or more individual amino acids which naturally occur in silk. The principal silk amino acids are glycine, alanine, 5 serine and tyrosine.
A silk amino acid mixture resulting from the hydrolysis of silk of low molecularweight and having a specific gravity of at least 1 is produced by Croda, Inc. and sold under the trade name "CROSILK LIQUID" which typically has a solids content in the range of 27 to 31% by weight. Further details of the silk amino acid mixture can be 10 found in Wendy W. Kim et al., U.S. Patent No. 4,906,460, incorporated herein by reference. A typical amino acid composition of "CROSILK LIQUID" is shown in the following Table .
AMINO ACIDPERCENT BY WEiGHT
Alanine 28.4 Givcine 2.0 Leucine 1.2 i~roline 1.2 Tvrosine o 6 i henvlalanine o g Serlne 1 s.4 Ar~inine -- _ 1 s As~arlic Acki 4 7 Gu~c AcW 4;1 Isoleucine o.s _ H~sticiine o. a Cvstine 01 Methionine 0 2 TOTAL 99.9 The instant compositions can contain a viscosity modifying solvent at a concentration of 0.1 to 5.0 weight percent, more preferably 0.5 to 4.0 weight percent.
The viscosity modifying agent is an alcohol of the formula 2127~ )7 wherein R1 = CH3, CH2CH3 R2 = CH3, CH2CH3 R3 = CH2OH, CH2CH2OH;
which is preferably 3-methyl-3-methoxy-butanol.
The 3-methyl-3-methoxy butanol is commercially avaiiable from Sattva Chemical Company of Stamford, Connecticut and Kuraray Co., Ltd., Osaka, Japan.
The instant composition can contain 0.1 to 4.0% of a protein selected from the group consisting of hydrolyzed animal collagen protein obtained by an enzymatic hydrolysis, lexeine protein, vegetal protein and hydrolyzed wheat protein and mixtures thereof.
The present light duty liquid detergents such as dishwashing liquids are readilymade by simple mixing methods from readily available components which, on storage, do not adversely affect the entire composition. However, it is preferred that the nonionic surfactant be mixed with the solubilizing ingredients, e.g., ethanol and, if present, prior to the addition of the water to prevent possible gelation. The nonionic based surfactant system is prepared by sequentially adding with agitation the anionic surfactant and the betaine to the nonionic surfactant, cosolubilizing agent and water, and then adding with agitation the formula amount of water to form an aqueous solution of the surfactant system. The use of mild heating (up to 1 00C.) assists in the solubilization of the surfactants. The viscosities are adjustable by changing the total percentage of active ingredienfs. No polymeric or clay thickening agent is added. In all such cases the product made will be pourable from a relatively narrow mouth bottle (1.5 cm. diameter) or opening, and the viscosity of the detergent formulation will not be so low as to be like water. The viscosity of the detergent desirably will be at least 100 centipoises (cps) at room temperature, but may be up to 1,000 centipoises as measured with a Brookfield Viscometer using a number 3 spindle rotating at 18 rpms.
Its viscosity may approximate those of cbmmercially acceptable detergents now on the market. The detergent viscosity and the detergent itself remain stable on storage for ,7,.. : ''' ' ''''' i :' ' ''"' ~ ' ' ' ' 2127~
,engthy periods of time, without color changes or ~ettling out of any insoluble materials. The pH of this formation is substantially neutral to skin, e.g., 4.5 to 8 and preferably 5 to 5.5. The compositions of the instant invention are optically clear - that is they exhibit a light transmission of at least 95%, more preferably at least 98%.
These products have unexpectedly desirably properties. For example, the foam quality and detersive property is equal to or better than standard light duty liquid detergents while using a nonionic surfactant as the primary surfactant and minimal amounts of anionic surfactant, thereby achieving a mild, non-irritating liquid detergent.
The following examples are merely illustrative of the invention and are not to be construed as limiting thereof.
E)(AMPLE 1 The following formulas were prepared at room temperature by simple liquid mixing procedures as previously described.
A B C
NEC~DOL 14 15.5 12.5 14.5 9~e~L~_ 7 5.5 ~--- 7 Na (AEOS.1~--11 5 10 5 10 5 Sod~ 3 0.05 0.05 0.03 Perfume 0.2 0.2 0.2 -~
Water Balance Balance Balance Mono ethanol amide 0 1 5 .
3.1 31 3 5 HEDT ~ 0.08 0.08 0 08 SheU Foam 2.0 2.0 2.0 S ~~
Brookfield viscosity~VTD~i~;~ 410 350 428 spindle, 18 rpms (cps) The Shell Foam and Shake Foam Height test were run against a control sample of a commercial Palmolive Skin Sensitive formulation manufactured by 20 Colgate-Palmolive Co. The designation "s" means that the sample being tested has the same value as the commercial sample. The designation "-" means that the value obtained is less than the value obtained for the commercial sample. The designation 2127 ~7 "+" means that the value obtained is superior to the value obtained for the commercial sample.
The following formula was prepared at room temperature by simple liquid mixing 5 procedures as previously described A
Nonionic Neodol 1-7 14.5 Elfan NS248 SMG (28% Al) 17.86 AEOSE08:1 Magnesium Salt Sodium lauryl sulfate (28%) 17 Cocoamido propyl betaine 16.67 30% Betadet HR-S(KAO) Vencol (progiven) 1.5 EDTA 0.1 Sodium formate 2.0 Sodium bisulfite 0.05 Perfume 0.2 Water Balance Appearance 5.0 : ~ -Brookfield vfscosity, RT #30 spindle, ~ 60~0 10 rpm (cps)
Claims (13)
1. A high foaming, light duty, liquid detergent composition comprising approximately, by weight, (a) 10% to 25% of a water soluble nonionic surfactant selected from the group consisting of primary and secondary C8-C18 alkanol condensates with 5 to 30 moles of ethylene oxide, condensates of C8-C18 alkylphenol with 5 to 30 moles of ethylene oxide and propylene oxide having a weight ratio of total alkylene oxide content of 60% to 85% by weight and condensates of 2 to 30 moles of ethylene oxide with sorbitan mono- and tri-C10-C20 alkanoic acid esters having an HLB of 8 to 15;
(b) 2% to 12% of a water soluble betaine surfactant; and (c) 8 to 16% of an ethoxylated alkyl ether sulfate surfactant; and (d) balance being water as an aqueous medium, wherein the surfactants are solubilized in the water and the composition does not contain amine oxides, calcium carbonate, polymeric or clay thickeners, abrasives, clays, silicas, alkyl glycine surfactants, cyclic imidinium surfactants or more than 3 wt.% of fatty acids or metal salts of fatty acids.
(b) 2% to 12% of a water soluble betaine surfactant; and (c) 8 to 16% of an ethoxylated alkyl ether sulfate surfactant; and (d) balance being water as an aqueous medium, wherein the surfactants are solubilized in the water and the composition does not contain amine oxides, calcium carbonate, polymeric or clay thickeners, abrasives, clays, silicas, alkyl glycine surfactants, cyclic imidinium surfactants or more than 3 wt.% of fatty acids or metal salts of fatty acids.
2. A liquid detergent composition according to Claim 1 further including 1.0 to 15% of a cosolubilizing agent selected from the group consisting of C2-C3 mono- and di-hydroxy alkanols, water soluble salts of C1-C3 substituted benzene sulfonate hydrotropes and mixtures thereof.
3. A liquid detergent composition according to Claim 2 wherein ethanol is present in an amount of 5% by weight or less.
4. A liquid detergent composition according to Claim 2 wherein the nonionic surfactant is a condensate of a primary C8-C18 alkanol with 5-30 moles of ethylene oxide.
5. A liquid detergent composition, according to Claim 1 further including a preservative.
6. A liquid detergent composition according to Claim 1 further including a color stabilizer.
7. A liquid detergent composition according to Claim 1 further including 0.5 to 8.0 wt.% of a cosolubilizing agent.
8. A high foaming, nonionic surfactant-based, light duty, liquid detergent composition comprising approximately, by weight:
(a) 10% to 20% of a water soluble nonionic surfactant selected from the group consisting of primary and secondary C8-C18 alkanol condensates with 5 to 30 moles of ethylene oxide, condensates of C8-C18 alkylphenol with about 5 to 30 moles of ethylene oxide, condensates of C8-C20 alkanol with a heteric mixture of ethylene oxide and propylene oxide having a weight ratio of ethylene oxide to propylene oxide from about 2.5:1 to 4:1 and a total alkylene oxide content of 60% to 85% by weight and condensates of about 2 to 30 moles of ethylene oxide with sorbitan mono- and tri-C10-C20 alkanoic acid esters having an HLB of 8 to 15;
(b) 0.5% to 8% of a magnesium salt of a C8-C18 ethoxylated alkyl ether sulfate surfactant;
(c) 0.5 to 8% of an alkali metal or ammonium salt of a C8-C14 alkyl sulfate surfactant;
(d) 2 to 10% of a water soluble betaine surfactant; and (e) balance being water as an aqueous medium, wherein the surfactants are solubilized in the water and the composition does not contain amine oxides, fatty acid alkanolamides, alkali metal or alkaline earth metal carbonates, clays, silicas, abrasives, polymeric or clay thickeners or more than 3 wt.% of fatty acids or metal salts of fatty acids.
(a) 10% to 20% of a water soluble nonionic surfactant selected from the group consisting of primary and secondary C8-C18 alkanol condensates with 5 to 30 moles of ethylene oxide, condensates of C8-C18 alkylphenol with about 5 to 30 moles of ethylene oxide, condensates of C8-C20 alkanol with a heteric mixture of ethylene oxide and propylene oxide having a weight ratio of ethylene oxide to propylene oxide from about 2.5:1 to 4:1 and a total alkylene oxide content of 60% to 85% by weight and condensates of about 2 to 30 moles of ethylene oxide with sorbitan mono- and tri-C10-C20 alkanoic acid esters having an HLB of 8 to 15;
(b) 0.5% to 8% of a magnesium salt of a C8-C18 ethoxylated alkyl ether sulfate surfactant;
(c) 0.5 to 8% of an alkali metal or ammonium salt of a C8-C14 alkyl sulfate surfactant;
(d) 2 to 10% of a water soluble betaine surfactant; and (e) balance being water as an aqueous medium, wherein the surfactants are solubilized in the water and the composition does not contain amine oxides, fatty acid alkanolamides, alkali metal or alkaline earth metal carbonates, clays, silicas, abrasives, polymeric or clay thickeners or more than 3 wt.% of fatty acids or metal salts of fatty acids.
9. A liquid detergent composition according to Claim 8 which includes, in addition, 1% to 15% by weight of a solubilizing agent selected from the group consisting of C2-C3 mono- or di-hydroxy alkanols, water soluble salts of C1-C3 substituted benzene sulfonate hydrotropes and mixtures thereof.
10. A liquid detergent composition according to Claim 9 wherein ethanol is present in an amount of 5% by weight or less.
11. A liquid detergent composition according to Claim 9 wherein the nonionic surfactant is a condensate of a primary C8-C18 alkanol with about 5 to 30 moles of ethylene oxide.
12. A liquid detergent composition according to Claim 8 further including a preservative.
13. A liquid detergent composition according to Claim 8 further including a color stabilizer.
Applications Claiming Priority (4)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US9151393A | 1993-07-09 | 1993-07-09 | |
| US9151293A | 1993-07-09 | 1993-07-09 | |
| US08/091,513 | 1993-07-09 | ||
| US08/091,512 | 1993-07-09 |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| CA2127657A1 true CA2127657A1 (en) | 1995-01-10 |
Family
ID=26784034
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| CA002127657A Abandoned CA2127657A1 (en) | 1993-07-09 | 1994-07-08 | High foaming nonionic surfactant based liquid detergent |
Country Status (10)
| Country | Link |
|---|---|
| EP (1) | EP0633308B1 (en) |
| AT (1) | ATE172487T1 (en) |
| AU (1) | AU6600394A (en) |
| CA (1) | CA2127657A1 (en) |
| DE (1) | DE69414040T2 (en) |
| DK (1) | DK0633308T3 (en) |
| ES (1) | ES2126080T3 (en) |
| GR (1) | GR940100343A (en) |
| NZ (1) | NZ260848A (en) |
| PT (1) | PT101539B (en) |
Cited By (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US6830755B2 (en) | 1999-10-01 | 2004-12-14 | Johnson & Johnson Consumer Companies, Inc. | Method for relaxing human beings using personal care compositions |
| US6986747B2 (en) | 2002-01-29 | 2006-01-17 | Johnson & Johnson Consumer Companies | Method of measuring the stress or relaxation level of a mammal |
Families Citing this family (14)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US5681852A (en) * | 1993-11-12 | 1997-10-28 | The Procter & Gamble Company | Desquamation compositions |
| CZ385896A3 (en) * | 1994-07-01 | 1997-08-13 | Procter & Gamble | Desquamation preparations |
| DE4444094A1 (en) * | 1994-12-10 | 1996-06-13 | Henkel Kgaa | Special non-ionic surfactants in hand dishwashing detergents |
| US5821237A (en) * | 1995-06-07 | 1998-10-13 | The Procter & Gamble Company | Compositions for visually improving skin |
| WO1997015650A1 (en) * | 1995-10-23 | 1997-05-01 | Colgate-Palmolive Company | Light duty liquid cleaning compositions |
| US5696073A (en) * | 1996-04-08 | 1997-12-09 | Colgate-Palmolive Co. | Light duty liquid cleaning composition |
| WO1997038073A1 (en) * | 1996-04-08 | 1997-10-16 | Colgate-Palmolive Company | Light duty liquid cleaning compositions |
| US5707955A (en) * | 1996-07-15 | 1998-01-13 | Colgate-Palmolive Co. | High foaming nonionic surfactant based liquid detergent |
| US5714454A (en) * | 1996-08-07 | 1998-02-03 | Colgate-Palmolive Co. | Light duty liquid cleaning compositions comprising alkyl sulroglycerides |
| WO1998005745A2 (en) * | 1996-08-08 | 1998-02-12 | Colgate-Palmolive Company | Light duty liquid cleaning compositions |
| US5767051A (en) * | 1997-02-13 | 1998-06-16 | Colgate Palmolive Company | Light duty liquid cleaning compositions |
| AU7263698A (en) * | 1997-05-02 | 1998-11-27 | Colgate-Palmolive Company, The | High foaming nonionic surfactant based liquid detergent |
| US6180582B1 (en) * | 1997-09-26 | 2001-01-30 | Colgate-Palmolive Co. | Liquid cleaning compositions |
| US6759382B2 (en) | 2001-06-01 | 2004-07-06 | Kay Chemical, Inc. | Detergent composition containing a primary surfactant system and a secondary surfactant system, and a method of using the same |
Family Cites Families (6)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US3928251A (en) * | 1972-12-11 | 1975-12-23 | Procter & Gamble | Mild shampoo compositions |
| US3950417A (en) * | 1975-02-28 | 1976-04-13 | Johnson & Johnson | High-lathering non-irritating detergent compositions |
| JPS60197614A (en) * | 1984-03-21 | 1985-10-07 | Shionogi & Co Ltd | Shampoo composition of low irritation |
| IE58219B1 (en) * | 1984-11-07 | 1993-08-11 | Procter & Gamble | Liquid detergent compositions |
| GB8905551D0 (en) * | 1989-03-10 | 1989-04-19 | Unilever Plc | Detergent compositions |
| PT101012B (en) * | 1991-11-07 | 1999-07-30 | Procter & Gamble | LIQUID DETERGENT COMPOSITIONS THAT UNDERSTAND CONVENTIONAL DETERGENTS AND COLOR STABILIZING COMPOUNDS |
-
1994
- 1994-06-24 NZ NZ260848A patent/NZ260848A/en unknown
- 1994-06-27 AU AU66003/94A patent/AU6600394A/en not_active Abandoned
- 1994-07-01 PT PT101539A patent/PT101539B/en not_active IP Right Cessation
- 1994-07-08 ES ES94401590T patent/ES2126080T3/en not_active Expired - Lifetime
- 1994-07-08 CA CA002127657A patent/CA2127657A1/en not_active Abandoned
- 1994-07-08 EP EP94401590A patent/EP0633308B1/en not_active Revoked
- 1994-07-08 DK DK94401590T patent/DK0633308T3/en active
- 1994-07-08 GR GR940100343A patent/GR940100343A/en unknown
- 1994-07-08 AT AT94401590T patent/ATE172487T1/en active
- 1994-07-08 DE DE69414040T patent/DE69414040T2/en not_active Revoked
Cited By (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US6830755B2 (en) | 1999-10-01 | 2004-12-14 | Johnson & Johnson Consumer Companies, Inc. | Method for relaxing human beings using personal care compositions |
| US6986747B2 (en) | 2002-01-29 | 2006-01-17 | Johnson & Johnson Consumer Companies | Method of measuring the stress or relaxation level of a mammal |
Also Published As
| Publication number | Publication date |
|---|---|
| EP0633308B1 (en) | 1998-10-21 |
| ES2126080T3 (en) | 1999-03-16 |
| PT101539B (en) | 1999-12-31 |
| ATE172487T1 (en) | 1998-11-15 |
| DE69414040D1 (en) | 1998-11-26 |
| NZ260848A (en) | 1996-08-27 |
| AU6600394A (en) | 1995-01-19 |
| DE69414040T2 (en) | 1999-06-17 |
| PT101539A (en) | 1995-05-04 |
| DK0633308T3 (en) | 1999-07-12 |
| GR940100343A (en) | 1995-10-31 |
| EP0633308A1 (en) | 1995-01-11 |
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Legal Events
| Date | Code | Title | Description |
|---|---|---|---|
| EEER | Examination request | ||
| FZDE | Discontinued |