CA2513438A1 - Personal care composition containing a cationic cellulose polymer and an anionic surfactant system - Google Patents

Abstract

The compositions of the present invention relate to personal cleansing compositions having from about 0.01 to about 5 wt.% of a cationic cellulose polymer; from about 5 to about 50 wt.% of an anionic surfactant system, having an ethoxylate level and a sulfate level wherein said ethoxylate level is in the amount of 1.04 multiplied by the molecular weight of said cationic cellulose polymer divided by 1,000,000 plus from about 0.75 to about 3.25, wherein said sulfate level is in the amount of 0.42 multiplied by the charge density of said cationic cellulose polymer plus from about 1.1 to about 3.6;
from about 0.01 to about 5 wt.% of a mono or divalent salt; and at least about 20 wt.% of an aqueous carrier.

Description

PERSONAL CARE COMPOSITION CONTAINING A
CATIONIC CELLULOSE POLYMER AND AN ANIONIC SURFACTANT SYSTEM
FIELD
The present invention relates to a personal care composition containing a cationic cellulose polymer and an anionic surfactant system. More specifically, it relates to a personal care composition containing an anionic surfactant system with specific ratios of ethoxylate and sulfate such that when combined with the cationic cellulose polymer, maximized levels of coacervate are achieved in use.
EACI~GROUND
Personal care compositions comprising various combinations of detersive surfactant and conditioning agents are known. These products typically comprise an anionic detersive surfactant in combination with a conditioning agent such as silicone, hydrocarbon oil, fatty esters, or combinations thereof. These products have become more popular among consumers as a means of conveniently obtaining hair and skin conditioning and cleansing performance all from a single personal care product.
However, many personal care compositions do not provide sufficient deposition of conditioning agents onto hair and skin during the cleansing process. Without such deposition, large proportions of conditioning agent are rinsed away during the cleansing process and therefore provide little or no conditioning benefit. Without sufficient deposition of the conditioning agent on the hair and skin, relatively high levels of conditioning agents may be needed in the personal cleansing composition to provide adequate conditioning performance. However, high levels of a conditioning agent can increase raw material costs, reduce lathering, and present product stability concerns.
Obtaining good deposition of a conditioning agent is further complicated by the action of detersive surfactants in the personal care composition. Detersive surfactants are designed to carry away or remove oil, grease, dirt, and particulate matter from the hair and skin. In doing so, the detersive surfactants can also interfere with deposition of the conditioning agent, and both deposited and non deposited conditioning agent can be removed during rinsing.
This fin-ther -- reduces deposition of the conditioning -agent onto-the hair-and -skin-halter rinsing, thus further reducing conditioning performance.
One known method for improving deposition of a conditioning agent involves the use of certain cationic deposition polymers. These polymers may be synthetic or naW
ral cellulosic or guar polymers that have been modified with cationic substituents. The cationic charge density of such polymers, especially when used in a personal care composition, is minimized so as to avoid incompatibility with anionic materials in the product such as anionic surfactant. Thus, most personal care compositions that contain both an anionic detersive surfactant and a cationic deposition polymer have a relatively low level of coacervate conditioning. A
need still exists for improved conditioning performance in personal care compositions.
SUMMARY
The present invention is directed to a personal care composition comprising:
a. from about 0.01 to about 5 wt.% of a cationic cellulose polymer, wherein said cationic cellulose polymer has a molecular weight of at least 800,000;
b. from about 5 to about 50 wt.% of an anionic surfactant system having an ethoxylate level and a sulfate level, i. wherein said ethoxylate level is in the amount of 1.04 multiplied by the molecular weight of said cationic cellulose polymer divided by 1,000,000 plus from about 0.75 to about 3.25, ii. wherein said sulfate level is in the amount of 0.42 multiplied by the charge density of said cationic cellulose polymer plus from about 1.1 to about 3.6;
c. from about 0.01 to about 5 wt.% of a mono or divalent salt; and d. at least about 20 wt.% of an aqueous carrier.
Alternatively, the present invention is directed to a personal care composition with a percent transmittance at 600nm of >_70% or a personal care composition with a cationic cellulose polymer having a molecular weight of at least 500,000 additionally comprising from about 0.01 to about 10 wt.% of a microemulsified oil having a particle size of __<80nm.
The present invention is further directed to a method of using the personal care C.O111pOS1t1011.
These and other features, aspects, and advantages of the present invention will beeome evident to those skilled in the art from a reading of the present disclosure.
DETAILED DESCRIPTION
While the specification concludes with claims tliat'particularly point out and distinctly claim the invention, it is believed the present invention will be better understood from the following description.

The personal care compositions of the present invention include a cationic cellulose polymer, an anionic surfactant system, a salt, and water. Each of these essential components, as well as preferred or optional components, are described in detail hereinafter.
All percentages, parts and ratios are based upon tile total weight of the compositions of the present invention, unless otherwise specified. All such weights as they pertain to listed ingredients are based on the active level and, therefore, do not include solvents or by-products that may be included in commercially available materials, unless otherwise specified. The ter111 "weight percent" may be denoted as "wt.%" herein.
All molecular weights as used herein are weight average molecular weights expressed as grams/mole, unless otherwise specified.
The term "charge density", as used herein, refers to the ratio of the number of positive charges on a monomeric unit of which a polymer is comprised to the molecular weight of said monomeric unit. The charge density multiplied by the polymer molecular weight determines the number of positively charged sites on a given polymer chain.
Herein, "comprising" means that other steps and other ingredients which do not affect the end result can be added. This term encompasses the telnls "consisting of and "consisting essentially of'. The compositions and methods/processes of the present invention can comprise, consist of, and consist essentially of the essential elements and limitations of the invention described herein, as well as any of the additional or optional ingredients, components, steps, or limitations described herein.
The term "polymer" as used herein shall include materials whether made by polymerization of one type of monomer or made by two (i.e., copolymers) or more types of 1110110111er S.
The term "solid particle" as used herein means a particle that is not a liquid or a gas.
The term "water soluble" as used herein, means that the polymer is soluble in water in the present composition. In general, the polymer should be soluble at 25" C at a concentration of U. l% by weight of the water solvent, preferably at 1%, more preferably at 5°,%, most preferably at 15%.
The tel°m "water insoluble" as used herein, Means that tile polymer is not soluble in water in the present composition. Thus, the polymer is not miscible with water.
The transparency of the-composition -is m~asured-using Ultra-VioletlVisible (UV/VIS) Spectrophotometry, which determines the absorption or transmission of UV/VIS
light by a sample. A light wavelength of 600 nm has been shown to be adequate for characterizing the degree of clarity of cosmetic compositions. Typically, it is best to follow the specific instructions relating the specific spectrophotometer being used. In general, the procedure for measuring percent transmittance starts by setting the spectrophotometer to the 600 nm.
Then a calibration "blank" is run to calibrate the readout to 100 percent transmittance. The test sample is then placed in a cuvette designed to fit the specific spectrophotomer and the percent transmittance is measured by the spectrophotomer at 600nm.
All cited references are incorporated herein by reference in their entireties.
Citation of any reference is not an admission regarding any determination as to its availabilifiy as priar art to the claimed invention.
While both the surfactant composition and polymer characteristics are known to impact conditioning efficacy, the Irnown art focuses on the polymer properties and fails to teach any specific surfactant composition. Moreover, the art generally teaches away from specific surfactant compositions and generally lists a broad range of suitable surfactants from which the composition may be selected.
One embodiment of the present invention concerns the surprising discovery that compositions combining certain specific levels and ratios of surfactant as described by the overall sulfate and ethoxylation values (described herein) maximize the conditioning benefit via maximization of coacervate formation. Moreover, while the optimum surfactant blend is different for each polymer, the authors have discovered that the optimum surfactant composition can be described by two parameters. These parameters include sulfate and ethoxylation values that when expressed as a function of the polymer's charge density and molecular weight maximize the formation of coacervate.
Coacervates, without being limited to a particular theory, provide improved hair and skin conditioning without any additional conditioning actives. Further, when dispersed conditioning agent droplets are added to the matrix, the coacervate provides an improved mechanism for conditioning agent deposition, yielding conditioning agent deposition that results in even more of a conditioning benefit.
A. Cationic Cell ~ul~s~ P~lymer The composition of the present invention includes a cationic cellulose polymer of sufficiently high molecular weight to effectively enhance the deposition of the personal care composition described herein. The average molecular weight of such suitable cationic cellulose polymers will generally be between about 500,000 and 10 million, preferably between about 800,000 and about 5 million, still more preferably between 1-- million- and 2.5 million. Suitable cationic cellulose polymers will have cationic charge densities of at least about 0.5 meq/gm, at the pH of intended use of the personal care composition, which pH will generally range from about pH 3 to about pH 9, preferably between about pH 4 and about pH 8. The "cationic charge density"
of a polymer, as that term is used herein, refers to the ratio of the number of positive charges on a monomeric unit of which the polymer is comprised to the molecular weight of said monomeric unit.
The concentration of the cationic polymer in the personal care composition ranges from about 0.01% to about 5.0%, preferably from about 0.05% to about 3.0% by weight of the personal care composition.
Suitable cationic cellulose polymers include those which conform to the Formula I:
R~
A-O-ER-N+-R3X

wherein A is an anhydroglucose residual group, such as a cellulose anhydroglucose residual; R is an alkylene oxyalkylene, polyoxyalkylene, or hydroxyalkylene group, or combination thereof; Rl, R2, and R3 independently are alkyl, aryl, alkylaryl, arylalkyl, alkoxyallcyl, or alkoxyaryl groups, each group containing up to about 18 carbon atoms, and the total number of carbon atoms for each cationic moiety (i.e., the sum of carbon atoms in Rl, R2 and R3) preferably being about 20 or less; and X is an anionic counterion. Any anionic counterions can be use in association with the cationic polymers of the present invention so long as the polymers remain soluble in water, in the personal care composition, or in a coacervate phase of the personal care composition, and so long as the counterions are physically and chemically compatible with the essential components of the personal care composition or do not otherwise unduly impair product performance, stability or aesthetics. Non limiting examples of such counterions include halides (e.g., chlorine, fluorine, bromine, iodine), sulfate and methylsulfate. The degree of cationic substitution in these polysaccharide polymers is typically from about 0.01-1 cationic groups per anhydroglucose unit.
Preferred cationic cellulose polymers are salts of hydroxyethyl cellulose reacted with trimethyl ammonium substituted epoxide, referred to in the industry (CTFA) as Polyquaternium and available from Amerchol Coip. (Edison, N.J., (JSA).
The cationic cellulose polymers herein are either soluble in the personal Cal'e 00111pOS1t1011 or are soluble in a complex coacervate phase in the personal care composition formed by the cationic cellulose polymer and the anionic surfactant component described herein. Complex coacervates of the cationic cellulose polymer cari also ve fonved with other charged materials in the personal care composition.
Coacervate formation is dependent upon a variety of criteria such as molecular weight, component concentration, and ratio of interacting ionic components, ionic strength (including modification of ionic strength, for example, by addition of salts), charge density of the cationic and anionic components, pH, and temperature. Coacervate systems and the effect of these parameters have been described, for example, by J. Caelles, et al., "Anionic and Cationic Compounds in Mixed Systems", Cosmetics & Toiletries, Vol. 106, April 1991, pp 49-54, C. J.
van Oss, "Coacervation, Complex-Coacervation and Flocculation", J. Dispersion Science and Technology, Vol. 9 (5,6), 1988-89, pp 561-573, and D. J. Burgess, "Practical Analysis of Complex Coacervate Systems", J. of Colloid and Interface Science, Vol. 140, No. 1, November 1990, pp 227-238, which descriptions are incorporated herein by reference.
It is believed to be particularly advantageous for the cationic cellulose polymer to be present in the personal care composition in a coacervate phase, or to form a coacervate phase upon application or rinsing of the personal care composition to or from the hair. Complex coacervates are believed to more readily deposited on the hair. Thus, in general, it is preferred that the cationic cellulose polymer exist in the personal care composition as a coacervate phase or form a coacervate phase upon dilution.
Techniques for analysis of formation of complex coacervates are known in the art. For example, microscopic analyses of the personal care compositions, at any chosen stage of dilution, can be utilized to identify whether a coacervate phase has formed. Such coacervate phase will be identifiable as an additional emulsified phase in the composition. The use of dyes can aid in distinguishing the coacervate phase from other insoluble phases dispersed in the personal care composition. In clear compositions, a spectrophotomer can also help determine at which dilution ratios) of water to personal care composition, the coacervate is most prevalent. For example, percent transmittance values measured of the dilution that are less than 85%
are indicative of significant coacervate formation. As percent transmittance values measured of the dilution decrease, typically higher levels of coacervate are formed.
Centrifuging the diluted personal care composition and measuring coacervate gravimetrically is an alternate quantitative technique applicable to opaque or clear compositions, and particularly advantageous in analyzing opaque products. Herein, several different dilutions were made in a 50m1 centrifuge tube and centrifuged for 20 minutes at 9200rpm using a Beckman Couller TJ25 centrifuge. The supernatant is then removed and the remaining settled coaeervatc;
assessed gravimetrically. A blank (shampoo without polymer] is run to establish a base line. The values are calculated for each dilution and the peal: amount reported from this method is referred herein'as via the coacervate ceritrifuge-rriethod~ ----- - --- -~-- ~ - --B. Anionic Surfactant System - Ethoxylate and Sulfate The personal care composition of the present invention includes an anionic surfactant.
The surfactant component is included to provide cleaning performance to the composition. The surfactant component in turn comprises an ethoxylated surfactant and a sulfate, and optionally a zwitterionic or amphoteric surfactant, an additional surfactant, or a combination thereof. Such surfactants should be physically and chemically compatible with the essential components described herein, or should not otherwise unduly impair product stability, aesthetics or performance.
Suitable anionic surfactant components for use in the personal care composition herein include those that are known for use in hair care or other personal care compositions. The concentration of the anionic surfactant component in the personal care composition should be sufficient to provide the desired cleaning and lather performance, and generally range from about 5% to about 50%, preferably from about 8% to about 30%, more preferably from about 10% to about 25%, by weight of the composition.
In considering the performance characteristics of coacervate generation, wet conditioning performance, dry conditioning performance, and conditioning ingredient deposition on hair, the present inventors discovered that in order to maximize the performance potential of polymer systems, it is necessary to optimize the levels and types of surfactant. The present inventors discovered that systems with ethoxylated and non-ethoxylated surfactants having a ratio of greater than 2:1 ethoxylated:non-ethoxylated surfactants had preferred performance, wherein the ethoxylated surfactants had greater than 2 moles of ethoxylation. The present inventors further discovered that in order to maximize the performance potential of polymer systems, it is necessary to optimize the levels of ethoxylate and sulfate. In order to do this, the aforementioned performance characteristics were plotted versus ethoxylate levels and versus sulfate levels. The "peals" or optimal level of sulfate and ethoxylate was then plotted versus a variety of chemical descriptors for cationic polymeric structures including molecular weight and charge density. The present inventors discovered that clear correlations existed with Rz>0.8, when the optimal level of etboxylate providing peals performance was plotted as the "y" axis versus polymer molecular weight divided by 1,000,000 as the "x" axis. The equation of that line showed that the slope of the line was equal to approximately 1.04 and the intercept fell between from about G.75 to about 3.25. Preferably the intercept is greater than 0.75, still preferably greater than 1.25, and still preferably greater than 1.75. Preferably the intercept is less than 3.25, still preferably less than 2.75, and still preferably less than 2.25. Thus, for any given molecular weight cationic cellulose polymer, an optimum ethoxylate level could be calculated. Additionally, a second correlation was developed where the optimal level of sulfate was-plotted as the "y"-axis-and charge density was plotted as the "x" axis. Again, a relatively straight line was realized where the slope of the line was equal to approximately 0.42 and the intercept fell between from about 1.1 to about 3.6.
Preferably, the intercept is greater than 1.1, still preferably greater than 1.6, and still preferably greater than 2.1. Preferably, the intercept is less than 3.6, still preferably less than 3.1, and still preferably less than 2.6. This discovery was surprising and explained how to maximize the performance of various polymers, particularly those polymers with molecular weights ranging from 500,000 to 2,000,000.
Thus, a percent ethoxylate can be calculated based on the stochiometry of the surfactant struchlre, based on a particular molecular weight of the surfactant where the number of moles of ethoxylation is known. Likewise, given a specific molecular weight of a surfactant and a sulfation reaction completion measurement, the percent sulfate can be calculated. Analytical techniques have been developed to measure percent ethoxylation or percent sulfates within surfactant systems. The level of ethoxylate and the level of sulfate representative of a particular surfactant system is calculated from the percent ethoxylation and percent sulfates of individual surfactants in the following manner:
Level of Ethoxylate in a composition = percent ethoxylation multiplied by percent active ethoxylated surfactant.
Level of Sulfate in a composition = percent Sulfate in ethoxylated surfactant multiplied by percent active ethoxylated surfactant plus percent sulfate in non-ethoxylated surfactant multiplied by percent active non-ethoxylated surfactant.
Sample Calculation:
Example 1 shows an ethoxylated surfactant that contains 0.294321% ethoxylate and a 0.188307%
sulfate level and a non-ethoxylated surfactant with a percent sulfate of 0.266845. Both surfactants are 29% active.
Level of Ethoxylate in Example 1 = 0.294321 multiplied by 10 (% active ethoxylated surfactant).
Thus the level of ethoxylate in Example 1's composition is approximately 2.94.
Level of Sulfate in Example 1 = 0.18830 multiplied by 1 U (% active ethoxylated surfactant) plus 0.266845 multiplied by 4 (% active non-ethoxylated surfactant). Thus the level of sulfate in Example 1's composition is approximately 2.95.
Preferred anionic surfactants suitable for use in-the personal care compositions are the alkyl sulfates and alkyl ether sulfates. These materials have the respective formulae ROSO3M
and RO(C2H40)xS03M, wherein R is alkyl or allcenyl of from about 8 to about 18 carbon atoms, x is an integer having a value of from about 1 to about 10, and M is a canon such as ammonium, alkanolamines, such as triethanolamine, monovalent metals, such as sodium and potassium, and polyvalent metal cations, such as magnesium, and calcium. Solubility of the surfactant will depend upon the particular anionic surfactants and canons chosen.
Preferably, R has from about 8 to about 18 carbon atoms, more preferably from about 10 to about 16 carbon atoms, even more preferably from about 12 to about 14 carbon atoms, in both the alkyl sulfates and alkyl ether sulfates. The alkyl ether sulfates are typically made as condensation products of ethylene oxide and monohydric alcohols having from about 8 to about 24 carbon atoms. The alcohols can be synthetic or they can be derived from fats, e.g., coconut oil, palm kernel oil, tallow. Lauryl alcohol and straight chain alcohols derived from coconut oil or palm kernel oil are preferred. Such alcohols are reacted with between from about 0 and about 10, preferably from about 2 to about 5, more preferably from about 3, molar proportions of ethylene oxide, and the resulting mixhlre of molecular species having, for example, an average of 3 moles of ethylene oxide per mole of alcohol, is sulfated and neutralized.
Specific non limiting examples of alkyl ether sulfates which may be used in the personal care compositions of the present invention include sodium and ammonium salts of coconut alkyl triethylene glycol ether sulfate, tallow alkyl triethylene glycol ether sulfate, and tallow alkyl hexa-oxyethylene sulfate. Highly preferred alkyl ether sulfates are those comprising a mixture of individual compounds, wherein the compounds in the mixture have an average alkyl chain length of from about 10 to about 16 carbon atoms and an average degree of ethoxylation of from about 1 to about 4 moles of ethylene oxide. Such a mixture also comprises from about 0 to 20% by weight C,~_i3 compounds; from 60 to 100% by weight Of Ci4-15-Iti compounds;
from about 0 to 20% by weight Of Cp_~g_19 COmpOtlIldS; from about 3 to 30% by weight of compounds having a degree of ethoxylation of 0; from about 45 to 90% by weight of compounds having a degree of ethoxylation of from 1 to 4~; from about 10 to 25% by weight of compounds having' a degree of ethoxylation of from 4 to 8; and from about 0.1 to 15% by weight of compounds having a degree of ethoxylation greater than 8.
Another suitable class of anionic surfactants are the v~ater-soluble salts of the organic, sulfuric acid reaction products of the general formula Ri-SO3-M wherein R, is chosen from the group consisting of a straight or branched chain, saturated aliphatic hydro-carbon radical having from 8 to 24~, preferably 12 to 18, carbon atoms; and M is a canon. Important examples are the sa-lts of an organic sulfuric-acrd reaction prozluct of a hydrocarbon of the methane series, including iso-, neo-, ineso-, and n-paraffins, having 8 to 24 carbon atoms, preferably 12 to 18 carbon atoms, and a sulfonating agent e.g., 503, HZS04, oleum, obtained according to known sulfonation methods, including bleaching and hydrolysis. Preferred are alkali metal and ammonium sulfonated C,Z_i$-n-paraffins.

Preferred anionic surfactants for use in the personal care compositions include ammonium lauryl sulfate, ammonium laureth sulfate, triethylamine lauryl sulfate, triethylamine laureth sulfate, triethanolamine lauryl sulfate, triethanolamine laureth sulfate, monoethanolamine lauryl sulfate, monoethanolamine laureth sulfate, diethanolamine lauryl sulfate, diethanolamine laureth sulfate, lauric monoglyceride sodium sulfate, sodium lauryl sulfate, sodium laureth sulfate, potassium lauryl sulfate, potassium laureth sulfate, sodium lauryl sarcosinate, sodium lauroyl sarcosinate, lauryl sarcosine, cocoyl sarcosine, ammonium cocoyl sulfate, ammonium lauroyl sulfate, sodium cocoyl sulfate, sodium lauroyl sulfate, potassium cocoyl sulfate, potassium lauryl sulfate, triethanolamine lauryl sulfate, triethanolamine lauryl sulfate, monoethanolamine cocoyl sulfate, monoethanolamine lauryl sulfate, and combinations thereof.
C. Additional Surfactants 1. wvitteri~nic or Amphoteric Surfactant Suitable amphotcric or zwitterionic surfactants for use in the personal care composition herein include those which are known for use in hair care or other personal care compositions.
Concentration of such amphoteric surfactants preferably ranges from about 0.5%
to about 20%, preferably from about 1 % to about 10%, by weight of the composition. Non limiting examples of suitable zwitterionic or amphoteric surfactants are described in U.S. Pat.
Nos. 5,104,646 (Bolich Jr. et al.), 5,106,609 (Bolich Jr. et al.), which descriptions are incorporated herein by reference.
Amphoteric surfactants suitable for use in the personal care composition are well known in the art, and include those surfactants broadly described as derivatives of aliphatic secondary and tertiary amines in which the aliphatic radical can be straight or branched chain and wherein one of the aliphatic substituents contains from about 8 to about 18 carbon atoms and one contains an anionic water solubilizing group such as carboxy, sulfonate, sulfate, phosphate, or phosphonate. Preferred amphoteric surfactants for use in the present invention include coeoamphoacetate, cocoamphodiacetate, lauroanlphoacetate, lauroamphodiacetate, and mixtures thereof ~Wittel-ionic surfactants suitable far use in the personal care composition are Well known in the art, and include those surfactants broadly described as derivatives of aliphatic duaternary ammomtnn, phosphomum, and sulfonium compounds, 111 which the allphatlc radicals Can be straight or branched chain, and wherein one of the aliphatic stlbstittlents contains from about 8 to about 18-carbon atoms--and-one contains an-anionic group such-as- carboxy, sulfonate, sulfate, phosphate or phosphonate. Zwitterionics such as betaines are preferred.
2. Optional Surfactants The personal care compositions of the present invention may further comprise additional surfactants for use in combination with the surfactant component described hereinbefore. Other suitable anionic surfactants are the water-soluble salts of organic, sulfuric acid reaction products conforming to the formula [ RI-S03-M ] where R1 is a straight or branched chain, saturated, aliphatic hydrocarbon radical having from about 8 to about 24, preferably from about 10 to about 18, carbon atoms; and M is a canon described hereinbefore. Non limiting examples of such surfactants are the salts of an organic sulfuric acid reaction product of a hydrocarbon of the methane series, including iso-, neo-, and n-paraffins, having from about 8 to about 24 carbon atoms, preferably about 12 to about 18 carbon atoms and a sulfonating agent, e.g., 503, H2S04, obtained according to known sulfonation methods, including bleaching and hydrolysis. Preferred are alkali metal and ammonium sulfonated C 10 to C 1 g n-paraffins.
Still other suitable anionic surfactants are the reaction products of fatty acids esterified with isethionic acid and neutralized with sodium hydroxide where, for example, tile fatty acids are derived from coconut oil or palm kernel oil; sodium or potassium salts of fatty acid amides of methyl tauride in which the fatty acids, for example, are derived from coconut oil or palm Kernel oil. Other similar anionic surfactants are described in U.S. Pat. Nos.
2,486,921; 2,486,922; and 2,396,278, which descriptions are incorporated herein by reference.
Other anionic surfactants suitable for use in the personal care compositions are the succinnates, examples of which include disodium N-octadecylsulfosuccinnate;
disodium lauryl sulfosuccinate; diammonium lauryl sulfosuccinate; tetrasodium N-(1,2-dicarboxyethyl)-N-octadecylsulfosuccinnate; diamyl ester of sodium sulfosuccinic acid; dihexyl ester of sodium sulfosuccinic acid; and dioctyl esters of sodium sulfosuccinic acid.
Other suitable anionic surfactants include olefin sulfonates having about 10 to about 24 carbon atoms. In this context, the tel'n1 "olefin sulfonates" refers to compounds which can be produced by the sulfonation of alpha-olefins by means of uncomplexed sulfur trioxide, followed by neutralization of the acid reaction mixture in conditions such that any sulfonates which have becn formed in the reachon are hydrolyzed to give the corresponding hydroxy-allanesulfonates.
The sulfur trioxide can be liquid or gaseous, and is usually, but not necessarily, diluted by inert diluents, for example by liquid 502, chlorinated hydrocarbons, etc., when used in the liquid form, or by air, nitrogen, gaseous 502, etc., when used in the gaseous form. The alpha-olefins ti~om which the olefin sulfonates are derived are mono-olefins having from about 10 to about 24 carbon atoms, preferably from about 12--to about 16-carbon atoms:-Preferably ~--they are straight chain olefins. In addition to the true allcene sulfonates and a proportion of hydroxy-alkanesulfonates, the olefin sulfonates can contain minor amounts of other materials, such as allcene disulfonates depending upon the reaction conditions, proportion of reactants, the naW re of the starting olefins and impurities in the olefin stock and side reactions during the sulfonation process. A non limiting example of such an alpha-olefin sulfonate mixture is described in U.S. Patent 3,332,880, which description is incorporated herein by reference.
Another class of anionic surfactants suitable fox use in the personal care compositions are the beta-alkyloxy alkane sulfonates. These surfactants conform to the Formula II:
ORZ H
R~ S03 M
H H
where R1 is a straight chain alkyl group having from about 6 to about 20 carbon atoms, R2 is a lower alkyl group having from about 1 to about 3 carbon atoms, preferably 1 carbon atom, and M
is a water-soluble canon as described hereinbefore. Preferred anionic surfactants for use in the personal care compositions include sodium tridecyl benzene sulfonate, sodium dodecyl benzene sulfonate.
Amides, including alkanol amides, are the condensation products of fatty acids with primary and secondary amines or alkanolamines to yield products of the general Formula III:
O
RC-N s X
~Y
wherein RCO is a fatty acid radical and R is Cg_20; X is an alkyl, aromatic or alkanol (CHR'CH20H wherein R' is H or Cl_6 alkyl); Y is H, alkyl, alkanol or X.
Suitable amides include, but are not limited to cocamide, lauramide, oleamide and stearamide.
Suitable alkanolamides include, but are not limited to, cocamide DEA, cocamide MEA, cocamide MIPA, isostearamide DEA, isostearamide MEA, isostearamide MIPA, lanolinamide DEA, lauramide DEA, lauramide MEA, lauramide MIPA, linoleamide DEA, linoleamide MEA, linoleamide MIPA, myristamide DEA, myristamide MEA, myristamide MIPA, Oleamide DEA, Oleamide MEA, Oleamide MIPA, pahnamide DEA, palmamide MEA, palmamide MIPA, palmitamide DEA, pahnitamide MEA, palm kernelamide DEA, palm kernelamide MEA, palm lcernelamide MIPA, peanutamide MEA, peanutamide MIPA, soyamide DEA, stearamide DEA, stearamide MEA, stearamide MIPA, tallamide DEA, tallowamide DEA, tallowamide MEA, undecylenamide DEA, undecylenamide MEA. The condensation reaction may be carried out with free fatty acids or with all types of esters of the fatty acids, such as fats and oils, and particularly methyl esters.
The reaction conditions and the raw material sources determine the blend of materials in the end product and the naW re of any impurities.
Suitable optional surfactants include nonionic surfactants. Any such surfactant known in the art for use in hair or personal care products may be used, provided that the optional additional surfactant is also chemically and physically compatible with the essential components of the personal care composition, or does not otherwise unduly impair product performance, aesthetics or stability. The concentration of the optional additional surfactants in the personal care composition may vary with the cleansing or lather performance desired, the optional surfactant selected, the desired product concentration, the presence of other components in the composition, and other factors well known in the art.
Non limiting examples of other surfactants suitable for use in the personal care compositions are described in McCutcheon's, Emulsifiers and Detergents, 1989 Annual, published by M. C. Publishing Co., and U.S. Pat. Nos. 3,929,678, 2,658,072; 2,438,091;
2,528,378, which descriptions are incorporated herein by reference.
D. M~n~ ~r Divalent Salt The personal care compositions of the present invention may further comprise a mono or divalent salt, which acts as a source of entropy in order to act as a coacervate initiator. Salt allows more contacts to be made between the polymer and surfactant, which increases the formation of coacervates. By the term "coacervate initiator", as used herein, means electrolytes capable of inducing the formation of coacervates when combined with compositions comprising an anionic detersive surfactant component surfactant system and the synthetic cationic polymer.
Surfactant salts themselves are not included in the present electrolyte definition but other salts are. Suitable salts include, but are not limited to chlorides, phosphates, sulfates, nitrates, citrates and halides. The counter ions of such salts can be, but are not limited to, sodium, potassium, ammonium, magnesium, zinc or other mono and divalent canon.
Electrolytes most preferred for use in the compositions of the present invention include sodium chloride, ammonium chloride, sodium citrate, magnesium chloride, and magnesium sulfate. It is recognized that these salts may serve as thickening aids or buffering aids in addition to their role as a coacervate initiator. The amount of coacervate initiator comprising the electrolyte and/or the optional surfactant will vary with the type of surfactant and polymer, but is preferably present at a level of fi°om about 0.01% to about 5°l0, more preferably from about 0.05% to about 3.Sal°, and still more preferably from about 0.1% to about 2%.
E. ~que~us Carrier The compositions of the present invention include an aqueous carrier. The level and species of the carrier are selected according to the compativility with other components and other desired characteristic of the product.
Garners useful in the present invention include water and water solutions of lower alkyl alcohols. Lower alkyl alcohols useful herein are monohydric alcohols having 1 to 6 carbons, more preferably ethanol and isopropanol.

Preferably, the aqueous carrier is substantially water. Deionized water is preferably used.
Water from natural sources containing mineral cations can also be used, depending oii the desired characteristic of the product. Generally, the compositions of the present invention comprise from about 20% to about 99%, preferably from about 40% to about 98%, and more preferably from about 60% to about 98% aqueous carrier.
The pH of the present composition is preferably from about 4 to about 9, more preferably from about 4.5 to about 7.5. Buffers and other pH adjusting agents can be included to achieve the desirable pH.
F. Optional Components 1. li~Iicroemulsified Conditioning Agents The personal care compositions of the present invention may further comprise microemulsified conditioning agents. These include materials used to give a particular conditioning benefit to hair and/or skin. The conditioning agents useful in the personal care compositions of the present invention typically comprise a water insoluble, water dispersible, non-volatile, liquid that forms emulsified, liquid particles or are solubilized by the surfactant micelles, in the anionic surfactant component. Suii:able conditioning agents for use in the personal care composition are those conditioning agents characterized generally as silicone oils, organic conditioning oils (e.g. hydrocarbon oils, polyolefins, fatty esters, and fatty alcohols), fluorinated compounds, or combinations thereof, or those conditioning agents which otherwise form liquid, dispersed, particles in the aqueous surfactant matrix herein. Such conditioning agents should be physically and chemically compatible with the essential components of the composition, and should not otherwise unduly impair product stability, aesthetics or performance.
The concentration of the conditioning agent in the personal care composition should be sufficient to provide the desired conditioning benefits, as will be apparent to one of ordinary skill in the art. Such concentration can vary with the canditioning agent, the conditioning perfarmance desired, the average size of the conditioning agent particles, the type and concentration of other components, and other lilts factors. The concentration of the conditioning agent may range from about 0.01 to about 10 weight percent and have a particle size of <80mn, preferably __<SOnm.
a. Silic~ne oils Silicone oils are flowable silicone materials having a viscosity, as measured at 25°C, less than l,-000,000 csk; preferablyfiom about 5 csh to about -1;0-00;000 cslc, more preferably from about 10 cslc to about 100,000 eslc. Suitable silicone oils for use in the personal care compositions of the present invention include polyallcyl siloxanes, polyaryl siloxanes, polyallcylaryl siloxanes, polyether siloxane copolymers, and mixtures thereof. Other insoluble, non-volatile silicone fluids having hair conditioning properties may also be used.

Silicone oils include polyalkyl or polyaryl siloxanes which conform to the following Formula IV:
R R R

R-5i-OSi-O Si-R

R R R

x wherein R is aliphatic, preferably alkyl or alkenyl, or aryl, R can be substituted or unsubstituted, and x is an integer from 1 to about 8,000. Suitable unsubstituted R groups for use in the personal care compositions of the present invention include, but are not limited to:
allcoxy, aryloxy, allcaryl, arylalkyl, arylallcenyl, alkamino, and ether-substituted, hydroxyl-substituted, and halogen-substituted aliphatic and aryl groups. Suitable R groups also include cationic amines and quaternary ammonium groups.
Preferred alkyl and alkenyl substituents are Ci to CS alkyls and alkenyls, more preferably from Ci to C4, more preferably from C, to C~. The aliphatic portions of other alkyl-, alkenyl-, or alkynyl-containing groups (such as alkoxy, alkaryl, and alkamino) can be straight or branched chains, and are preferably from C~ to C5, more preferably from Ci to C4, even more preferably from C, to C3, more preferably from C, to CZ. As discussed above, the R
StIbStlttlelltS Can alSO
contain amino functionalities (e.g. alkamino groups), which can be primary, secondary or tertiary amines or quaternary ammonium. These include mono-, di- and tri- allcylamino and allcoxyamino groups, wherein the aliphatic portion chain length is described above.
b. Organic conditioning oils The conditioning component of the personal care compositions of the present invention may also comprise from about 0.05% to about 3%, by weight of the composition, preferably from about 0.08% to about 1.5%, more preferably from about 0.1 % to about 1 %, of at least one organic conditioning oil as the conditioning agent, either alone or in combination with other conditioning agents, such as the silicone oils (described above).
i. Hydrocarbon oils Suitable organic conditioning oils for use as conditioning agents in the personal care compositions of-the--present--invention-include, but are-not limi-ted-to;
hydrocarbon oils having at least about 10 carbon atoms, such as cyclic hydrocarbons, straight chain aliphatic hydrocarbons (saturated or unsaturated), and branched chain aliphatic hydrocarbons (saturated or unsaturated), including polymers and mixtures thereof. Straight chain hydrocarbon oils preferably are from about Ci2 to about Ci~. Branched chain hydrocarbon oils, including hydrocarbon polymers, typically will contain more than 19 carbon atoms.
Specific non-limiting examples of these hydrocarbon oils include paraffin oil, mineral oil, saturated and unsaturated dodecane, saturated and unsaturated tridecane, saturated and unsahlrated tetradecane, saturated and unsaturated pentadecane, saturated and unsaturated hexadecane, polybutene, polydecene, and mixtures thereof. Branched-chain isomers of these compounds, as well as of higher chain length hydrocarbons, can also be used, examples of which include highly branched, saturated or unsaturated, allcanes such as the permethyl-substituted isomers, e.g., the permethyl-substituted isomers of hexadecane and eicosane, such as 2, 2, 4, 4, 6, 6, 8, 8-dimethyl-10-methylundecane and 2, 2, 4, 4, 6, 6-dimethyl-8-methylnonane, available from Pennethyl Corporation. Hydrocarbon polymers such as polybutene and polydecene. A
preferred hydrocarbon polymer is polybutene, such as the copolymer of isobutylene and butane. A
commercially available material of this type is L-14 polybutene from Amoco Chemical Corporation.
ii. P~lyolefins orgalllC COlldltlOrilllg oils for use in the personal care compositions of the present invention can also include liquid polyolefms, more preferably liquid poly-a-olefins, snore preferably hydrogenated liquid poly-a-olefins. Polyolefins for use herein are prepared by polymerization of C4 to about C~4 olefenic monomers, preferably from about C~
to about C,~.
Non-limiting examples of olefenic monomers for use in preparing the polyolefin liquids herein include ethylene, propylene, 1-butane, 1-pentane, 1-hexane, 1-octane, 1-decene, 1-dodecene, 1-tetradecene, branched chain isomers such as 4-methyl-1-pentane, and mixt<Ires thereof. Also suitable for preparing the polyolefin liquids are olefin-containing refinery feedstoclcs or effluents. Preferred hydrogenated a.-olefin monomers include, but are not limited to: 1-hexane to 1-hexadecenes, 1-octane to 1-tetradecene, and mixtures thereof.
iii. Fatty l~sters ~ther suitable organic conditioning oils for Llse as the conditioning agent in the personal care compositions of the present invention include, but are not limited to, fatty esters having at least 10 carbon atoms. These fatty este'rs~ include esters with hydrocarby~
chains derived from fatty acids or alcohols (e.g. mono-esters, polyhydric alcohol esters, and di-and tri-carboxylic acid esters). The hydrocarbyl radicals of the fatty esters hereof may include or have covalently bonded thereto other compatible functionalities, such as amides and alkoxy moieties (e.g., ethoxy or ether linkages, etc.).

Specific examples of preferred fatty esters include, but are not limited to:
isopropyl isostearate, hexyl laurate, isohexyl laurate, isohexyl palmitate, isopropyl pahnitate, decyl oleate, isodecyl oleate, hexadecyl stearate, decyl stearate, isopropyl isostearate, dihexyldecyl adipate, lauryl lactate, myristyl lactate, cetyl lactate, oleyl stearate, oleyl oleate, oleyl myristate, lauryl acetate, cetyl propionate, and oleyl adipate.
Other fatty esters suitable for use in the personal care compositions of the present invention are mono-carboxylic acid esters of the general formula R'COOR, wherein R' and R are alkyl or allcenyl radicals, and the sum of carbon atoms in R' and R is at least 10, preferably at least 22.
Still other fatty esters suitable for use in the personal care compositions of the present invention are di- and tri-alkyl and alkenyl esters of carboxylic acids, SLICK
as esters Of C4 to Cs dicarboxylic acids (e.g. Ci to C2~ esters, preferably C, to C~, of succinic acid, glutaric acid, adipie acid,). Specific non-limiting examples of di- and tri- alkyl and allcenyl esters of carboxylic acids include isocetyl stearyol stearate, diisopropyl adipate, and tristearyl citrate.
Other fatty esters suitable for use in the personal care compositions of the present invention are those known as polyhydric alcohol esters. Such polyhydric alcohol esters include allcylene glycol esters, such as ethylene glycol mono and di-fatty acid esters, diethylene glycol mono- and di-fatty acid esters, polyethylene glycol mono- and di-fatty acid esters, propylene glycol mono- and di-fatty acid esters, polypropylene glycol monooleate, polypropylene glycol 2000 monostearate, ethoxylated propylene glycol monostearate, glyceryl mono-and di-fatty acid esters, polyglycerol poly-fatty acid esters, ethoxylated glyceryl monostearate, 1,3-butylene glycol monostearate, 1,3-butylene glycol distearate, polyoxyethylene polyol fatty acid ester, sorbitan fatty acid esters, and polyoxyethylene sorbitan fatty acid esters.
Still other fatty esters suitable for use in the personal care compositions of the present invention are glycerides, including, but not limited to, mono-, di-, and tri-glycerides, preferably di-and tri-glycerides, more preferably triglycerides. For use in the personal care compositions described herein, the glycerides are preferably the mono-, di-, and tri-esters of glycerol and long chain carboxylic acids, such as C,o to C~~ carboxylic acids. A variety of these types of materials can be obtained from vegetable and animal fats and oils, such as castor oil, safflower oil, cottonseed oil, corn oil, olive oil, cod liver oil, almond oil, avocado oil, palm oil, sesame oil, -lanolin-and soybean oil. -Synthetic oils inclttde;-but are not liW ited-tb,'triolein and tristearin glyceryl dilaurate.
Other fatty esters suitable for use in the personal care compositions of the present invention are water insoluble synthetic fatty esters. Some preferred synthetic esters conform to the general Formula V:

O

R~- IC-O Y

n wherein R' is a C~ to C~ alkyl, alkenyl, hydroxyallcyl or hydroxyalkenyl group, preferably a saturated alkyl group, more preferably a saW rated, linear, alkyl group; n is a positive integer having a value from 2 to 4, preferably 3; and Y is an alkyl, alkenyl, hydroxy or carboxy substituted alkyl or alkenyl, having from about 2 to about 20 carbon atoms, preferably from about 3 to about 14 carbon atoms. Other preferred synthetic esters conform to the general Formula VI:
O
R~-O-IC Y
n wherein RZ is a C8 to Cio alkyl, alkenyl, hydroxyalkyl or hydroxyalkenyl group; preferably a saturated alkyl group, more preferably a saturated, linear, alkyl group; n and Y are as defined above in Formula V.
Specific non-limiting examples of suitable synthetic fatty esters for use in the personal care compositions of the present invention include: P-43 (C$-C,o triester of trimethylolpropane), MCP-684 (tetraester of 3,3 diethanol-1,5 pentadiol), MCP 121 (C$-Cio diester of adipic acid), all of which are available from Mobil Chemical Company.
c. Fluorinated Compounds Fluorinated compounds suitable for delivering conditioning to hair or skin consistent with the present invention include perfluoropolyethers, perfluorinated olefins, fluorine based specialty polymers that may be in a fluid or elastomer form similar to the silicone fluids previously described, and perfluorinated dimethicones Specific non-limiting examples of suitable fluorinated compounds include the Fomblin product line from Ausimont which include HC/04, HC/25, HCO1, HC/02, HC/03; Dioctyldodecyl Fluoroeptyl Citrate, commonly called Biosil Basics Fluoro Gerbet 3.5 supplied by Biosil Technologies; and Biosil Basics Fluorosil LF also supplied by Biosil TeChIlOlOgleS.
2. Dispersed, ~atcc° lnsolublc Particles One embodiment of the present invention comprises dispersed, water insoluble particles.
Particles useful in the present invention can be inorganic, synthetic, or semi-synthetic in composition Non limiting examples of inorganic particles include various silica particles including colloidal silicas, fumed silicas, precipitated silicas and silica gels. Non-limiting examples of colloidal silicas include Snowtex C, Snowtex O, Snowtex 50, Snowtex OL, Snowtex ZL available from Nissan Chemical America Corporation and colloidal silicas sold under the tradename Ludox available from W.R. Grace & Co. Non-limiting examples of fumed silicas include hydrophillic and hydrophobic forms available as Aerosil 130, Aerosil 200, Aerosil 300, Aerosil 8972 and Aerosil 8812 available from Degussa Coip. and those available from Cabot Corp.
under the trade name Cab-O-Sil including Cab-O-Sil M-5, HS-5, TS-530, TS-610, and TS-720. Non-limiting examples of precipitated silicas include those available in both hydrophillic and hydrophobic versions from Degussa Corp. under the trade name Sipernat including Sipernat 350, 360, 22LS, 225, 320, SOS, D10, D11, D17, and C630; those sold by W. R. Grace & Co. under the trade name Syloid, those sold by the J.M. Huber Corp. under the tradename Zeothix and Zeodent, and those available from Rhodia under the trade name Tixosil. Also useful in the present invention are spherical silica particles available in various particle sizes and porosities.
Non limiting examples of spherical silica particles include MSS-500/H, MSS-500/3H, MSS-500, MSS-500!3, MSS-500/N and MSS-500/3N available from LOBO Products Inc.; those available from Presperse Inc.
under the trade name Spheron including Spheron P-1500 and L-1500, and those available from Sunjin Chemical Co. under the trade name Sunsil including Sunsil 20, 20L, 20H, SOL, 50, SOH, 130L, 130 and 130H. Other non-limiting examples of inorganic particles usefial in the present invention include variaus silicates including magnesium silicate such as those available from 3M
under the trade name CM-111 Cosmetic Microspheres, glass particles such as those available from Nippon Paint Corp. under the trade name GlamurGlo Glass Chips and PrizmaLite Glass Spheres; tales, micas, sericites, and various natural and synthetic clays including bentonites, hectorites, and montmorillonites.
Examples of synthetic particles include nylon, silicone resins, poly(~neth)acrylates, polyethylene, polyester, polypropylene, polystyrene, polyurethane, polyamide, epoxy resins, urea resins, and acrylic powders. Non limiting examples of useful particles are Microease 1 lOS, I 145, 116 (micronized synthetic waxes), Micropoly 210, 2505 (micronized polyethylene), Microslip (micronized polytetrafluoroethylene), and Microsillc (combination of polyethylene and polytetrafluoroethylene), all of which arc available from Micro Powder, Inc.
Other examples include MP-2200, BPA-500 (polymethylmethacrylate), EA-209 (ethylen e/aerylate copolymer), SP-501(nylon-12), SP-10 (nylon-12), ES-830 (polymethly methacrylate), BPD-80U, BPD-500, BPA-500 (polyurethane), and CL2080 (polyethylene) particles available from Lobo Products, Inc., spherical polyethylenes available from Quantum Chemical under the trade name Microthene - including-MN701; MN710; MN=714, MN-722~and---FN51-OO; nylon particles available from Elf Atochem under the trade name Orgasol, acrylates copolymers available from Advanced Polymer Systems under the trade name Microsponge and Polytrap, and silicone resins sold under the name Tospearl particles by GE Silicones. Ganzpearl GS-0605 crosslinlced polystyrene (available from Presperse) is also useful.

Non limiting examples of hybrid particles include Ganzpearl GSC-30SR (Sericite &
crosslinlced polystyrene hybrid powder), and SM-1000, SM-200 (mica and silica hybrid powder available from Presperse).
Particles comprised of polymers and copolymers obtained from esters, such as, for example, vinyl acetate or lactate, or acids, such as, for example, itaconic, citraconie, malefic or fumaric acids may also be used. See, in this regard, Japanese Patent Application No. JP-A-2-112304, the full disclosure of which is incorporated herein by reference.
3. Suspending agent The personal care compositions of the present invention may further comprise a suspending agent at concentrations effective for suspending the water-insoluble, dispersed material in the personal care compositions. Such concentrations range from about 0.1% to about 10%, preferably from about 0.3% to about 5.0%, by weight of the personal care compositions.
Suitable suspending agents include crystalline suspending agents that can be categorized as aryl derivatives, long chain amine oxides, or combinations thereof. These suspending agents are described in U.S. Patent 4,741,855, which description is incorporated herein by reference.
4. Anti-dandruff Actives The compositions of the present invention may also contain an anti-dandruff agent.
Suitable, non-limiting examples of anti-dandruff particulates include;
pyridinethione salts, azoles, selenium sulfide, particulate sulfur, and mixtures thereof. Preferred are pyridinethione salts.
Such anti-dandruff particulate should be physically and chemically compatible with the essential components of the composition, and should not otherwise unduly impair product stability, aesthetics or performance. These anti-dandruff actives are described in WO01/00151 which description is incorporated herein by reference.
5. Humcctant The compositions of the present invention may contain a humectant. The humectants herein are selected from the group consisting of polyhydric alcohols, water soluble allcoxylated nonionic polymers, and mixtures thereof. The h umectants, when used herein, are preferably used at levels by weight of the composition of from about 0.1 % to about 20%, more preferably fi-orn about 0.5% to about 5%.
Polyhydric-alcolrols useful -herein include-glyc-erin; sorbitol, propylene glycol, butylene glycol, hexylene glycol, ethoxylated glucose, l, 2-hexane diol, hexanetriol, dipropylene glycol, erythritol, trehalose, diglycerin, xylitol, maltitol, maltose, glucose, fructose, sodium chondroitin sulfate, sodium hyaluronate, sodium adenosine phosphate, sodium lactate, pyrrolidone carbonate, glucosamine, cyclodextrin, and mixtures thereof.

Water soluble allcoxylated nonionic polymers useful herein include polyethylene glycols and polypropylene glycols having a molecular weight of up to about 1000 such as those with CTFA names PEG-200, PEG-400, PEG-600, PEG-1000, and mixtures thereof.
6. Other Optional Components The compositions of the present invention may contain fragrance.
The compositions of the present invention may also contain vitamins and amino acids such as: water soluble vitamins such as vitamin B1, B2, B6, B12, C, pantothenic acid, pantothenyl ethyl ether, panthenol, biotin, and their derivatives, water soluble amino acids such as asparagine, alanin, indole, glutamic acid and their salts, water insoluble vitamins such as vitamin A, D, E, and their derivatives, water insoluble amino acids Such as tyrosine, tryptamine, and their salts.
The compositions of the present invention may also contain pigment materials such as inorganic, nitroso, monoazo, disazo, carotenoid, triphenyl methane, triaryl methane, xanthene, quinaline, oxazine, azine, antliraquinone, indigoid, thionindigoid, quinacridone, phthalocianine, botanical, natural colors, including: water soluble components such as those having C. I. Names.
The CO111p051t10riS Of the present invention may also contain antimicrobial agents which are useful as cosmetic biocides and antidandruff agents including: water soluble components such as piroctone olamine, water insoluble components such as 3,4,4'-trichloroearbanilide (trichlosan), triclocarban and zinc pyrithione. The compositions of the present invention may also contain chelating agents.
METHOD OF MAKING
The compositions of the present invention, in general, may be made by mixing the ingredients together at either room temperature or at elevated temperature, e.g., about 72°
C. Heat only needs to be used if solid ingredients are in the composition. The ingredients are mixed at the batch processing temperature. Additional ingredients, including electrolytes, polymers, and particles, may be added to the product at room temperature.
METHOD OF llSE
The personal care compositions of the present invention are used in a conventional manner for cleansing and conditioning hair or skin. An effective amount of the composition for cleansing and-conditioning~the hair or slein is applied to the hair or skin, that has preferably been wetted with water, and then rinsed off. Such effective amounts generally range from about lgm to about SOgm, preferably from about lgm to about 20gm. Application to the hair typically includes working the composition through the hair such that most or all of the hair is contacted with the composition.

This method for cleansing and conditioning the hair or skin comprises the steps of:
a) wetting the hair or skin with water, b) applying an effective amount of the personal care composition to the hair or skin, and c) rinsing the applied areas of skin or hair with water. These steps can be repeated as many times as desired to achieve the desired cleansing and conditioning benefit.
NON-LIMITING EXAMPLES
The compositions illustrated in the following Examples illustrate specific embodiments of the compositions of the present invention, but are not intended to be limiting thereof. Other modifications can be undertaken by the skilled artisan without departing from the spirit and scope of this invention. These exemplified embodiments of the composition of the present invention provide enhanced deposition of the personal care composition due to enhanced coacervate formation.
The compositions illustrated in the following Examples are prepared by conventional formulation and mixing methods, an example of which is described above. All exemplified amounts are listed as weight percents and exclude minor materials such as diluents, preservatives, color solutions, imagery ingredients, botanicals, and so forth, unless otherwise specified.
The following are representative of Clear Shampoo compositions (shampoo compositions with a %Transmittance >_70%) of the present invention:

Exam les, wt%

In redient 1 2 3 4 5 6 7 8 Water q.s. q.s. q.s. q.s. q.s, q.s. q.s. q.s.

Pol uaterium 10 0.25 0.25 0.25 0.25 ~

Pol uaterium 10 0.50 Z

Pol uaterium 10 0.50 Cationic Cellulose 0.50 Pol mer A 4 Cationic Cellulose 0.50 Pol mer B 5 Sodium Laureth 34.4841.3841.3848.2834.4834.4831.0334.48 Sulfate (SLE3S-29% active) ~

Sodium Lauryl 13.796.9 6.9 10.3513.7913.7913.7913.79 Sulfate (SLS - 29% active ' Dimethicone 1.0 - 1.0 2.0 2.0 2.0 2.0 Microemulsion TEA Dodedeyl Benzene 0.45 SLIlfOllate ~

POE Laur 1 Ether 0.1 ~

Disodium Coco 4.44 4.44 4.44 4.44 Am hodiacetate ~ ~

PPG-2 Hydroxyethyl2 2 2 2 2 2 2 2 Coco/Isostearamide ~Z

Magnesium Chloride,0.5 0.5 0.5 0.5 hexah drate ~

Sodium Chloride 0.5 0.5 0.5 0.1 1.0 1.0 1.0 0.5 ~4 Fra rance 0.55 0.55 0.55 0.5 0.5 0.5 0.75 0.55 Preservatives, Up Up Up Up Up Up Up Up pH to to to to to to to to ad'usters 1% 1% 1% 1% 1% 1% 1% 1%

Calculated:

Ethox late level 2.94 3.53 3.53 4.12 2.94 2.94 2.65 2.94 Sulfate level 2.95 2.95 2.95 3.4~ 2.95 2.95 2.76 2.95 UCare Polymer JR30M, MW=2.0 MM, charge density = 1.32 meq./gram, supplier Dow Chemicals UCare Polymer ICG30M, MW= 2.OMM, charge density =1.96 meq./gram, supplier Dow Chemicals 3 Ucare Polymer LR30M, MW= 1.8MM, charge density = 0.71 meq/grams, supplier Dow Chemicals 4 Cationic Cellulose polymer with MW = 2.0 MM and charge density = 0.7 . 5 Cationic Cellulose polymer with MW= 1.0 MM and charge density = 1.29 6 Sodium Laureth Sulfate-at 29% active with-an average of approximately 3 moles of ethoxylation, supplier: P&G

7 Sodium Lauryl Sulfate at 29% active, supplier: P&G

8 DC2-1870, 30nm particle size dimethicone using TEA dodecyl benzene sulfonte and POE lauryl ether as primary surfactants, supplier Dow Corning.

9 Biosoft N-300 (60% active), supplier Steppan BRIJ 35, Supplier Unichema 11 Schercoteric MS-2 at 45% active, supplier Scher Chemicals 12 Promidium 2, supplier Unichema 13 Magnesium Chloride 6-Hexahydrate, supplier Fisher Chemicals 14 Sodium Chloride USP (food grade), supplier Morton.
The following are representative of Shampoo compositions of the present invention:
Exam les, wt%

In redient 9 10 11 12 13 Water .s. .s. .s. .s. .s.

Polymer LR30M ~ 0.25 Pol mer JR30M 2 0.5 Pol mer KG30M 3 0.5 0.5 Cationic Cellulose Pol 0.5 mer 4 Sodium Laureth Sulfate 51.72 37.93 34.48 SLE3) 5 Sodium Laureth Sulfate(SLE2S) 48.3 G

Sodium Laur 1 Sulfate' 17.24 10.35 13.34 Ammonium Laureth Sulfate 30.11 (ALE3S) $

Ammonium Lauryl Sulfate 6.8 '' Silicone Microemulsion 2.0 2.0 ~

Octadodec 1 Stearate 0.5 ~ ~

Cet 1 Alcohol ~2 0.5 TEA Dodec 1 Benzene 0.5 Sulfonate ~

POE Laur 1 Ether ~4 0.25 Cocoamdo ro 1 Betaine 2.0 ~5 Sodium Coco Am hoacetate 2.0 4.44 ~G

Cocamide MEA " 0.94 PPG-2 Hydroxyethyl 3 3 Coco/Isostearamide'$

Sodium Chloride ~~ 0.5 1.5 1.0 1.0 1.2 Fra rance 0.55 0.55 0.75 0.5 0.5 Preservatives, H ad'usters< 1.0 < 1.0 < 1.0 < 1.0 < 1.0 Calculated levels based on surfactants added above:

Ethox late level 4.41 2 2 3.24 3.12 2.94 Sulfate level 4.16 1.9 2.87 2.90 2.92 1 Ucare Polymer LR30M, MW= 1.BMM, charge density = 0.71 me~lgrams, supplier _ . Dow Chemicals _ . _._. . _ . .. _. _ 2 UCare Polymer JR30M, MW=2.0 MM, charge density = 1.32 meq./gram, supplier Dow Chemicals 3 UCare Polymer I~G30M, MW= 2.OMM, charge density =1.96 meq./gram, supplier Dow Chemicals 4 Cationic Cellulose polymer with MW = 2.0 MM and charge density = 0.7 Sodium Laureth Sulfate at 29% active with an average of approximately 3 moles of ethoxylation, supplier: P&G
6 Sodium Laureth Sulfate at 29% active with an average of approximately 2 moles of ethoxylation, supplier: P&G
7 Sodium Lauryl Sulfate at 29% active, supplier: P&G
8 Ammonium Laueth Sulfate. 25% active with 3 moles of ethoxylation, supplier:
P&G
9 Ammonium Lauryl Sulfate, 25% active, supplier: P&G

10 DC2-1550, 44 nm particle size dimethicone using TEA dodecyl benzene sulfonte and POE lauryl ether as primary surfactants, supplier Dow Corning.

11 Ceraphyl ODS, supplier: ISP

12 CO-1695, supplier P&G

13 Biosoft N-300 (60% active), supplier Steppan 14 BRIJ 35, Supplier Unichema 15 Tegobetaine (30% active), supplier Goldschmidt (Degussa) 16 Schercoteric MS at 50% active, supplier Scher Chemicals, Inc.

17 Monamide CMA, supplier Unichema 18 Promidium 2, supplier Unichema 19 Sodium Chloride USP (food grade), supplier Morton.
Examples 14, 16 and 17 are additional highly preferred examples. Example 15 is very similar in composition to example 14, but has a different surfactant ethoxylate value. Example 15 has a calculated ethoxylate value below the claimed range and performs poorly with respect to coacervate formation. Example 18, lileewise has a similar composition to the highly preferred example 16, but has a different surfactant ethoxylate value, again below the preferred range, Example 18 has poor coacervate formation and is not a preferred composition.
These examples highlight the importance of ethoxylate ratio and demonstrate that relatively small changes in ethoxylate value have an unexpectedly dramatic impact on coacervate amount.
This observation by the present inventors that only very specific ethoxylate values yield optimum coacervate amount and moreover the dependence of this value on the polymer molecular weight is novel with respect to the known art which often fails to identify any specific ethoxylate values or eduivalent (such as precise levels and ratios of ethoxylated surfactant).

Exam les, wt%

In redient 14 15 16 17 18 Water .s. .s. .s. .s. .s.

Pol mer LR30M ~ 0.25 0.25 Pol mer I~G30M 2 0.25 0.25 0.25 Sodium Laureth Sulfate 51.73 SLE3) 3 Sodium Laur 1 Sulfate 4 17.244 ' Ammonium Laureth Sulfate 57.2 40.0 6_0.0 _40.0 (ALE3S) 5 Ammonium Laur 1 Sulfate 6.8 28.0 20.0 28_.0 ~

Silicone Microemulsion' 2.0 2.0 2.0 1.0 2.0 Cocamide MEA $ 0.94 0.94 0.94 0.94 0.94 Sodium Chloride '' 1.3 1.3 0.50 A111111011111n1 Chloride 0.29 0.20 ~

AXS ~ ~ 0.5 Fra rance 0.55 0.55 0.55 0.55 0.55 Preservatives, H ad'usters< 1.0 < 1.0 < 1.0 < 1.0 < 1.0 Calculated levels based on surfactants added above:

Ethox late level 4.21 2.95 4.41 4.41 2.94 Sulfate level 15 3.75 4.16 4.16 3.75 3.

Coacervate % ~z ~ _ - 4.5 .. 8.6 3.0 _ I 25.0 ~
_ I
9.0 ~

1 Ucare Polymer LR30M, MW= 1.8MM, charge density = 0.71 meq/grams, supplier Dow Chemicals 2 UCare Polymer I~G30M, MW= 2.OMM, charge density =1.96 meq./granl, supplier Dow Chemicals 3 Sodium Laureth Sulfate at 29% active with an average of approximately 3 moles of ethoxylation, supplier: P&G
4 Sodium Lauryl Sulfate at 29% active, supplier: P&G
Ammonium Laueth Sulfate. 25% active with 3 moles of ethoxylation, supplier:
P&G
6 Ammonium Lauryl Sulfate, 25% active, supplier: P&G
7 DC2-1550, 44~ nm particle size dimethicone using TEA dodecyl benzene sulfonte and P~E lauryl ether as primary surfactants, supplier Dow Corning.
8 Monamide CMA, supplier Unichema 9 Sodium Chloride USP (food grade), supplier Morton.
Ammonil.lm Chloride, supplier P~cG.
11 Alnmonllnn %ylene Sulphate, supplier Stepan 12 Calculated via the coaccrvate centrifuge method - described herein The following are representative of Body Wash compositions of the present invention.
Exam le, wt%

In redient 19 20 21 22 Water .s. .s. .s. .s.

Pol mer JR30M ' 0.5 Pol mer I~G30M 2 0.5 0.5 0.5 Sodium Laureth Sulfate (SLE3)41.38 41.38 50.0 41.38 Sodium Lauryl Sulfate 4 6.9 13.79 10.0 13.79 Silicone Microemulsion 5 2.0 1.0 Ce 1 Alcohol G 0.5 Disodium Laureth Sulfosuccinate1.0 ' Gl cerine ~ 1.0 2.0 Cocoamdo ro 1 Betaine ~ 3.0 Disodium Coco Am hodiacetate' 4~.44~ 1.0 4.44 Dec 1 Glucoside " 1.0 Glyceryl Stearate, Cetearyl 0.5 Alcohol, Stearic Acid, 1-Propanamimium-3-Amino-N-(2-hydroxyethyl)N,N-Dimethyl-N-C

18 Acr 1 Derivs., Chlorides'Z

Perfluoro of meth liso ro 1.0 1 Ether'4 Ma nesium Chloride, hexahydrate'S0.5 Sodium Chloride'" 0.55 0.6 1.0 0.6 Fra rance 0.55 0.55 0.55 0.55 Preservatives, H ad'usters < 1.0 < 1.0 < 1.0 < 1.0 Calculated levels based on surfactants added above:

Ethox late level 3.53 3.53 4.27 3.53 Sulfate level 2.79 3.33 3.50 3.33 1 UCare Polymer JR30M, MW=2.0 MM, charge density = 1.32 meq./gram, supplier Dow Chemicals 2 UCare Polymer I~G30M, MW= 2.OMM, charge density =1.96 meq./gram, supplier Dow Chemicals 3 Sodium Laureth Sulfate at 29% active with an average of approximately 3 moles of ethoxylation, supplier: P&G
4 Sodium Lauryl Sulfate at 29% active, supplier: PEG
S DC2-1870, 30nm particle size dimethicon a using TEA dodecyl benzene sulfonte and P~E lauryl ether as primary surfactants, supplier Dow Corning.
6 C~-1695, supplier P&G
7 Stepan-MILD LSB, supplier Steppan 8 Star, supplier: Procter & Gamble 9 Tegobetaine (30% active), supplier Goldschmidt (Degussa) Schercoteric MS=2 at 45%-active,-supplier Scher~Chenricals;-Inc. ~ --11 Plantaren PS-100, supplier Cognis Care Chemicals 12 Prolipid 151, supplier ISP
13 Promidium 2, supplier Unichema 14 Fomblin HC/04, supplier Ausimont Magnesium Chloride 6-Hexahydrate, supplier Fisher Chemicals 16 Sodium Chloride USP (food grade), supplier Morton.

All documents cited in the Detailed Description of the Invention are, in relevant part, incorporated herein by reference; the citation of any document is not to be construed as an admission that it is prior art with respect to the present invention.
While particular embodiments of the present invention have been illustrated and described, it would be obvious to those skilled in the art that various other changes and modifications can be made without departing from the spirit and scope of the invention. It is, therefore, intended to cover in the appended claims all such changes and modifications that are within the scope of this invention.

Claims (28)

1. A personal care composition comprising:
a. from 0.01 to 5 wt.% of a cationic cellulose polymer, wherein said cationic cellulose polymer has a molecular weight of at least 800,000;
b, from 5 to 50 wt.% of an anionic surfactant system having an ethoxylate level and a sulfate level, i. ~wherein said ethoxylate level is in the amount of 1.04 multiplied by the molecular weight of said cationic cellulose polymer divided by 1,000,000 plus from 0.75 to 3.25, ii. ~wherein said sulfate level is in the amount of 0.42 multiplied by the charge density of said cationic cellulose polymer plus from 1.1 to 3.6;
c. from 0.01 to 5 wt.% of a mono or divalent salt; and d. at least 20 wt.% of an aqueous carrier.

2. The personal care composition of claim 1 wherein said cationic cellulose polymer has a molecular weight of at least 1.0 million.

3. The personal care composition of claim 1 wherein said cationic cellulose polymer has a charge density of at least 0.5 meq/gm.

4. The personal care composition of claim 1 wherein said cationic cellulose polymer is present in a concentration of from 0.1 wt.% to 2.0 wt.%.

5. The personal care composition of claim 1 wherein said cationic cellulose polymer is Polyquaternium 10.

6. The personal care composition of claim 1 wherein said cationic cellulose polymer is in a coacervate phase or forms a coacervate phase upon dilution.

7. The personal care composition of claim 1 wherein said anionic surfactant system has a ratio of ethoxylated to nonethoxylated surfactant greater than 2:1 and the ethoxylated surfactant contains at least 2 moles of ethoxylation.

8. ~The personal care composition of claim 1 wherein said anionic surfactant system is selected from the group consisting of alkyl sulfates, alkyl ether sulfates, and mixtures thereof.

9. ~The personal care composition of claim 1 further comprising zwitterionic or amphoteric surfactants in a concentration of from 0.5 wt.% to 20 wt.%.

10. ~The personal care composition of claim 1 wherein said mono or divalent salt is selected from the group consisting of chlorides, phosphates, sulfates, nitrates, citrates, halides, and mixtures thereof.

11. ~The personal care composition of claim 1 wherein said mono or divalent salt is present in a concentration of from 0.05 wt.% to 3.5 wt.%.

12. ~The personal care composition of claim 1 further comprising dispersed, water insoluble particles.

13. ~The personal care composition of claim 1 wherein said personal care composition has a percent transmittance at 600nm of >=70%.

14. ~A personal care composition comprising:
a. ~from 0.01 to 5 wt.% of a cationic cellulose polymer, wherein said cationic cellulose polymer has a molecular weight of at least 500,000;
b, ~from 5 to 50 wt.% of an anionic surfactant system, having an ethoxylate level and a sulfate level i. wherein said ethoxylate is in the amount of 1.04 multiplied by the molecular weight of said cationic cellulose polymer divided by 1,000,000 plus from 0.75 to 3.25 ii. wherein said sulfate level is in the amount of 0.42 multiplied by the charge density of said cationic cellulose polymer plus from 1.1 to 3.6;
c. ~from 0.01 to 5 wt.% of a mono or divalent salt;
d. ~from 0.01 to 10 wt.% of a conditioning agent having a particle size of <=80nm, and e, ~at least 20 wt.% of an aqueous carrier.

15. ~The personal care composition of claim 14 wherein said cationic cellulose polymer has a molecular weight of at least 1.0 million.

16. ~The personal care composition of claim 14 wherein said cationic cellulose polymer has a charge density of at least 0.5 meq/gm.

17. ~The personal care composition of claim 14 wherein said cationic cellulose polymer is present in a concentration of from 0.1 wt.% to 2.0 wt.%.

18. ~The personal care composition of claim 14 wherein said cationic cellulose polymer is Polyquaternium 10.

19. ~The personal care composition of claim 14 wherein said cationic cellulose polymer is in a coacervate phase or forms a coacervate phase upon dilution.

20. ~The personal care composition of claim 14 wherein said anionic surfactant system has a ratio of ethoxylated to nonethoxylated surfactant greater than 2:1 and the ethoxylated surfactant contains at least 2 moles of ethoxylation.

21. ~The personal care composition of claim 14 wherein said anionic surfactant system is selected from the group consisting of alkyl sulfates, alkyl ether sulfates, and mixtures thereof.

22. ~The personal care composition of claim 14 further comprising zwitterionic or amphoteric surfactants in a concentration of from 0.5 wt.% to 20 wt.%.

23. ~The personal care composition of claim 14 wherein said mono or divalent salt is selected from the group consisting of chlorides, phosphates, sulfates, nitrates, citrates, halides, and mixtures thereof.

24. ~The personal care composition of claim 14 wherein said mono or divalent salt is present in a concentration of from 0.05 wt.% to 3.5 wt.%.

25. ~The personal care composition of claim 14 farther comprising dispersed, water insoluble particles.

26. ~The personal care composition of claim 14 wherein said conditioning agent is selected from the group consisting of silicone oils, hydrocarbon oils, polyolefins, fatty esters, fluorinated compounds, and mixtures thereof.

27. ~The personal care composition of claim 14 wherein said conditioning agent has a particle size of <= 50nm.

28. ~A method of treating hair or skin by administering a safe and effective amount of said personal care compositions.