NZ234293A - Personal cleansing compositions containing a surfactant and a bulky amine cationic polymer - Google Patents

Personal cleansing compositions containing a surfactant and a bulky amine cationic polymer

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Publication number
NZ234293A
NZ234293A NZ234293A NZ23429390A NZ234293A NZ 234293 A NZ234293 A NZ 234293A NZ 234293 A NZ234293 A NZ 234293A NZ 23429390 A NZ23429390 A NZ 23429390A NZ 234293 A NZ234293 A NZ 234293A
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NZ
New Zealand
Prior art keywords
polymer
odor
amine
cationic
personal cleansing
Prior art date
Application number
NZ234293A
Inventor
Robert Gregory Bartolo
Louis Fay Wong
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Procter & Gamble
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Publication date
Application filed by Procter & Gamble filed Critical Procter & Gamble
Publication of NZ234293A publication Critical patent/NZ234293A/en

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Classifications

    • CCHEMISTRY; METALLURGY
    • C11ANIMAL OR VEGETABLE OILS, FATS, FATTY SUBSTANCES OR WAXES; FATTY ACIDS THEREFROM; DETERGENTS; CANDLES
    • C11DDETERGENT COMPOSITIONS; USE OF SINGLE SUBSTANCES AS DETERGENTS; SOAP OR SOAP-MAKING; RESIN SOAPS; RECOVERY OF GLYCEROL
    • C11D3/00Other compounding ingredients of detergent compositions covered in group C11D1/00
    • C11D3/16Organic compounds
    • C11D3/37Polymers
    • C11D3/3703Macromolecular compounds obtained otherwise than by reactions only involving carbon-to-carbon unsaturated bonds
    • C11D3/373Macromolecular compounds obtained otherwise than by reactions only involving carbon-to-carbon unsaturated bonds containing silicones
    • C11D3/3742Nitrogen containing silicones
    • CCHEMISTRY; METALLURGY
    • C11ANIMAL OR VEGETABLE OILS, FATS, FATTY SUBSTANCES OR WAXES; FATTY ACIDS THEREFROM; DETERGENTS; CANDLES
    • C11DDETERGENT COMPOSITIONS; USE OF SINGLE SUBSTANCES AS DETERGENTS; SOAP OR SOAP-MAKING; RESIN SOAPS; RECOVERY OF GLYCEROL
    • C11D17/00Detergent materials or soaps characterised by their shape or physical properties
    • C11D17/0047Detergents in the form of bars or tablets
    • C11D17/006Detergents in the form of bars or tablets containing mainly surfactants, but no builders, e.g. syndet bar
    • CCHEMISTRY; METALLURGY
    • C11ANIMAL OR VEGETABLE OILS, FATS, FATTY SUBSTANCES OR WAXES; FATTY ACIDS THEREFROM; DETERGENTS; CANDLES
    • C11DDETERGENT COMPOSITIONS; USE OF SINGLE SUBSTANCES AS DETERGENTS; SOAP OR SOAP-MAKING; RESIN SOAPS; RECOVERY OF GLYCEROL
    • C11D3/00Other compounding ingredients of detergent compositions covered in group C11D1/00
    • C11D3/16Organic compounds
    • C11D3/20Organic compounds containing oxygen
    • C11D3/22Carbohydrates or derivatives thereof
    • C11D3/222Natural or synthetic polysaccharides, e.g. cellulose, starch, gum, alginic acid or cyclodextrin
    • C11D3/227Natural or synthetic polysaccharides, e.g. cellulose, starch, gum, alginic acid or cyclodextrin with nitrogen-containing groups
    • CCHEMISTRY; METALLURGY
    • C11ANIMAL OR VEGETABLE OILS, FATS, FATTY SUBSTANCES OR WAXES; FATTY ACIDS THEREFROM; DETERGENTS; CANDLES
    • C11DDETERGENT COMPOSITIONS; USE OF SINGLE SUBSTANCES AS DETERGENTS; SOAP OR SOAP-MAKING; RESIN SOAPS; RECOVERY OF GLYCEROL
    • C11D3/00Other compounding ingredients of detergent compositions covered in group C11D1/00
    • C11D3/16Organic compounds
    • C11D3/37Polymers
    • C11D3/3746Macromolecular compounds obtained by reactions only involving carbon-to-carbon unsaturated bonds
    • C11D3/3769(Co)polymerised monomers containing nitrogen, e.g. carbonamides, nitriles or amines
    • CCHEMISTRY; METALLURGY
    • C11ANIMAL OR VEGETABLE OILS, FATS, FATTY SUBSTANCES OR WAXES; FATTY ACIDS THEREFROM; DETERGENTS; CANDLES
    • C11DDETERGENT COMPOSITIONS; USE OF SINGLE SUBSTANCES AS DETERGENTS; SOAP OR SOAP-MAKING; RESIN SOAPS; RECOVERY OF GLYCEROL
    • C11D3/00Other compounding ingredients of detergent compositions covered in group C11D1/00
    • C11D3/16Organic compounds
    • C11D3/37Polymers
    • C11D3/3746Macromolecular compounds obtained by reactions only involving carbon-to-carbon unsaturated bonds
    • C11D3/3769(Co)polymerised monomers containing nitrogen, e.g. carbonamides, nitriles or amines
    • C11D3/3773(Co)polymerised monomers containing nitrogen, e.g. carbonamides, nitriles or amines in liquid compositions

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  • Chemical & Material Sciences (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Organic Chemistry (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Oil, Petroleum & Natural Gas (AREA)
  • Wood Science & Technology (AREA)
  • Engineering & Computer Science (AREA)
  • Health & Medical Sciences (AREA)
  • Molecular Biology (AREA)
  • Emergency Medicine (AREA)
  • Detergent Compositions (AREA)
  • Cosmetics (AREA)
  • Compositions Of Macromolecular Compounds (AREA)
  • Addition Polymer Or Copolymer, Post-Treatments, Or Chemical Modifications (AREA)

Description

New Zealand Paient Spedficaiion for Paient Number £34293 /Ti ~ / / : : . .So•to-.'ifj' , U ^ I ! n-c C0.03.b7l,- o\os\SO. 1 2 6 AUG 1993 m.( NEW ZEALAND PATENTS ACT, 1953 No.: Date: NEW ZEAL'W1;) patent Ofrct 28 JUNJ990 RECEIVED COMPLETE SPECIFICATION 'PERSONAL CLEANSING PRODUCT WITH ODOR COMPATIBLE BULKY AMINE CATIONIC POLYMER" XD^ffWc, THE PROCTER & GAMBLE COMPANY, a corporation organised under the laws of the State of Ohio, United States of America, located at One Procter & Gamble Plaza, Cincinnati, Ohio 45202, United States of America. h'freby declare the. invention for which we pray that a patent may be granted to rTOE^us, and the method by which it is to be performed, to be pa.rticula rly described in and by the following statement: - - 1 - (followed by page la) - la - PERSONAL CLEANSING PRODUCT WITH ODOR COMPATIBLE BULKY AMINE CATIONIC POLYMER FIELD OF THE INVENTION This invention pertains to personal cleansing compositions for personal washing, which compositions comprise quaternary amine polymers.
BACKGROUND OF THE INVENTION Liquid and solid bar compositions based on soap and/or synthetic surfactants are commonly used for cleansing the human body. A wide variety of additives have been suggested for inclusion in said compositions. Some enhance the physical properties, e.g., bar hardness, wear rate, resistance to water. Others enhance the in-use properties such as lather characteristics and some impact on the impression the composition has on the skin both during washing (bar feel) and afterwards.
It has been discovered that the addition of certain polymeric materials to such liquids and bars can have a beneficial skin mildness effect for the user without deleteriously affecting other product properties. In general, the useful polymers should be soluble or dispersible in water to a level of at least 1% by weight, preferably at least 5% by weight at 25°C. Suitable polymers are high molecular weight materials (mass-average molecular weight determined, for instance, by light scattering, being generally from about 20,000 to about 5,000,000, preferably from about 50,000 to about 4,000,000, and more preferably from about 500,000 to about 3,000,000) and preferably have a thickening ability such that a 1% dispersion of the polymer in water at 20"C exceeds about 1 PaS(10 poise) at a shear rate of 10"2 sec'l. Useful polymers are the cationic, nonionic, amphoteric, and anionic polymers useful in the cosmetic field. Preferred are cationic and nonionic resins and mixtures thereof. Highly preferred are the cationic resins.
To date the preferred cationic polymers include cationic guar gums such as hydroxyproxyltrimethylammonium guar gum. 23 4 2 However, it has been discovered that there is an odor problem with using such "cationic trimethylamine quaternized polymers" in compositions having a pH of 7.5 or above. They break down and release odoriferous labile amines.
Odoriferous labile amines are detectable at levels as low as 2 ppb. Personal cleansing products containing odoriferous quaternary amine polymers are disclosed in one or more of the following patents: Pat .. No.
Date Inventorf s) US 3,761,418 9/1973 Parran, Jr.; US 4,234,464 11/1980 Morshauser; US 4,061,602 12/1977 Oberstar et al.; US 4,472,297 9/1984 Bolich et al.; us 4,491,539 1/1985 Hoskins et al.; us 4,540,507 9/1985 Grol1ier; us 4,673,525 6/1987 Smal 1 et al.; us 4,704,224 11/1987 Saud; and Jap . J57105 6/30/82 Pol a.
All of the above patents are hereby incorporated herein by reference, especially their for basic personal cleansing product and quat polymer disclosures.
SUMMARY OF THE INVENTION The present invention relates to a personal cleansing product made with a selected quaternized cationic polymer wherein each quaternary ammonium moiety is derived from a bulky amine. The preferred product is a toilet bar.
OBJECTS OF THE INVENTION An object of the present invention is to provide an improved toilet bar, preferably a soap bar, comprising a cationic polymeric skin conditioning agent which does not comprise a potential odoriferous amine moiety.
Other objects will become apparent from the detailed description below.
DETAILED DESCRIPTION OF THE INVENTION The present invention comprises basic personal cleansing compositions comprising from about 0.2% to about 5% by weight selected cationic polymer wherein each cationic group is derived from a "bulky" amine. Compared to personal cleansing compositions 2 3 4.9 0 7 "»>* r.J which are prepared with cationic polymers which comprise a potential labile amine moiety, e.g., trimethylamine-based cationic polymers, the compositions of this invention consistently exhibit superior odor stability due to the selected "bulky amine" cationic 5 polymers. The term "basic personal cleansing compositions" as used herein means that the composition has a pH of at least about 7.5, preferably at least about 8.5.
While not being bound to any theory, illustrations A and B show the theoretical degradation of labile amine containing 10 cationic polymers in a basic environment. Generic degradation: (A) Polymer-CHR-CH2-N+(CH3)3 > polymer-CR=CH2 + N(CH3)3 where R can be meant to represent any group (e.g., H, OH, alkyl chain); e.g., (B) Guar-ch2-0-ch2-CH(0h)-ch2-N+(ch3)3 > Guar-CH2-0-CH2- C(0H)=ch2 + N(ch3)3 The extent of this degradation and the effect of it on product odor were not appreciated heretofore. The level of hydration required to cause a problem is very low and therefore it is extremely difficult to detect and identify the offending 20 material.
The Bulky Amine Cationic Polymers Bulky amine polymers are defined herein as POLYMERS with the following non-labile cationic functional group: (I) (POLYMER)-CRlH-CR2R3-NR4R5R6 wherein R1-R3 is H or any 25 other substituent and R^, R^ and R& combine with N to form an amine with less odor impact than trimethylamine, preferably at least one of R^, R^ and R^ is alkyl having a chain length of from about 2 to about 24 carbon atoms, or an alkoxy alkyl group containing from about 2 to about 12 carbon atoms. 3Q Some examples of preferred bulky amine polymers are cationic guar gums having the following structures: (II) Ci2H25 I Guar-ch2-0-ch2-CH(0h)-ch2-N+ch3 I CH3 23 4 >;; (iii) ch2ch2oh I Guar-CH2-0-CH2-CH(0H)-CH2-N+CH3 I CH3 An example of a bulky amine hydroxyethyl cellulose (HEC) polymer is: (IV) Cl2H25 I hec-ch2-0-ch2-ch(0h)-ch2-n+ch3 I CHj These "bulky amine" groups add additional complexity to the preparation of the polymer and the finished compositions. They would not be used, except for the existence of the odor problem with the trimethylamine derived polymer. They may also have improved skin conditioning benefits.
The composition of this invention preferably comprises from about 0.2% to about 5%, preferably from about 0.5% to about 2%, of the cationic polymer. The average molecular weight of the preferred cationic guar gum is from about 50,000 to about 1,000,000, preferably from about 100,000 to about 500,000, and more preferably from about 250,000 to about 400,000 and the degree of substitution is from about 0.5 to about 4, preferably from about 1 to about 2.5. Some preferred cationic guars (galactomannans) are disclosed in U.S. Pat. No. 4,758,282, Stober et al., issued July 19, 1988, incorporated herein by reference. The cationic guar gum polymers disclosed in commonly assigned U.S. Pat. Application Ser. No. 07/266,039, J.R. Knochel and P.E. Vest, filed Nov. 2, 1988, would be suitable when the cationic groups are substituted with bulky amine groups.
Other bulky amine cationic polymeric skin conditioning agents useful in the present invention have molecular weights of from 1,000 to 3,000,000. Useful polymers are selected from the group consisting of: (I) cationic polysaccharides; (II) cationic copolymers of saccharides and synthetic cationic monomers, and 2 3 4 2 9 3 (III) synthetic polymers selected from the group consisting of any other synthetic polymer containing pendant quaternary amine groups, e.g., quaternized silicones and quaternized methacrylates.
Specific examples of members of the bulky amine cationic polysaccharide class include the cationic hydroxyethyl cellulose, e.g., LM-200 made by Union Carbide Corporation.
The cationic copolymers of saccharides and synthetic cationic monomers useful in the present invention encompass those con-10 taining the following saccharides: glucose, galactose, mannose, arabinose, xylose, fucose, fructose, glucosamine, galactosamine, glucuronic acid, galacturonic acid, and 5 or 6 membered ring polyalcohols. Also included are hydroxymethyl, hydroxyethyl and hydroxypropyl derivatives of the above sugars. 15 The boiling points of some exemplary substituted amines are set out in Table 1.
TABLE 1 Eliminated Amine Boilinq Point/'C Labile Amine Trimethylamine 3 Bulky Amine Dimethylethylamine 36 Methyldiethylamine 63 Triethyl amine 89 Dimethyloctylamine 195 Dimethylcyclohexylamine 158 Dimethyl benzyl amine 183 Dimethylethanolamine 133 Diethylethanolamne 161 For a homologous series of compounds (e.g., tri-substituted amines), volatility decreases with increasing molecular weight. Volatility is dependent, among other things on the boiling point of the neat component. Odor impact also has a strong dependence on the amount of volatilized material that reaches the nose.
Table 1 demonstrates, the significant effect which adding "bulky" groups has on volatility and, hence, odor impact of amines. For pure hydrocarbon substitution, the larger the alkyl chains (or the 23 4 2 9 larger the degree of long chain substitution) the lower the odor impact. Thus, bulky amines have boiling points of greater than ambient temperature, and preferably at least about 30"C, more preferably more than about 80*C.
The Surfactant Component The surfactant component of the present compositions comprises alkali metal soap or synthetic surfactant or mixtures thereof.
Alkali metal soaps can be made by direct saponification of 10 the fats and oils or by the neutralization of the free fatty acids which are prepared in a separate manufacturing process. Particularly useful are the sodium and potassium salts of the mixtures of fatty acids derived from coconut oil and tallow, i.e., sodium and potassium tallow and coconut soaps.
The term "tallow" is used herein in connection with fatty acid mixtures which typically have an approximate carbon chain length distribution of 2.5% Ci4, 29% C]5, 23% Cis, 2% palmitoleic, 41.5% oleic and 3% linoleic. (The first three fatty acids listed are saturated.) Other mixtures with similar distribution, such as 20 the fatty acids derived from various animal tallows. The tallow can also be hardened (i.e., hydrogenated) to convert part or all of the unsaturated fatty acid moieties to saturated fatty acid moieties.
When the terms "coconut oil" and "coconut fatty acid" (CNFA) 25 are used herein, they refer to fatty acid mixtures which typically have an approximate carbon chain length distribution of about 8% C7, 7% CjOi 48% C12' 17% C14, 9% C]6, 2% C18» 7% oleic, and 2% linoleic. (The first six fatty acids listed are saturated.) Other sources having similar carbon chain length distribution such 30 as palm kernel oil and babassu kernel oil are included with the terms coconut oil and coconut fatty acid.
A preferred soap bar of this invention comprises soap as its primary or sole surfactant It also contains as an essential ingredient a skin conditioning amount of a hydrated, cationic guar 35 gum provided by a cationic guar gum polymer. This polymer is uniformly distributed in the soap bar matrix without affecting the smooth feel of the dry or wet bar. 234293 7 Another preferred toilet bar is based on mild synthetic surfactants as disclosed in commonly assigned U.S. Pat. No. 4,673,525, Small et al., issued June 16, 1987, incorporated herein by reference.
Synthetic detergents can also be present in compositions herein. Preferred types of synthetic detergents are of the anionic or nonionic type. Examples of anionic synthetic detergents are the salts of organic sulfuric reaction products such as alkyl sulfates having the formula R24OSO3M; alkyl sulfonates having the formula R24SO3M; alkyl ether sulfates having the formula R24(0C2H4)X0S03M; alkyl mono glyceride sulfonates having the formula In the above formulae, R24 is a straight or branched chain alkyl of from about 8 to about 24 carbon atoms; M is an alkali metal or ammonium ion; x is a number of from 1 to about 10; y is a number of from 1 to 4; and X is selected from the group consisting of chlorine, hydroxyl, and -SO3M, at least one X in each molecule being -SO3M. Examples of nonionic synthetic detergents are ethoxylated fatty alcohols (e.g., the reaction product of one mole of coconut fatty alcohol with from about 3 to about 30 moles of ethylene oxide) and fatty acid amides such as coconut fatty acid monoethanolamide and stearic acid diethanolamide. Although it may be desirable in some instances to incorporate synthetic detergents into the compositions of the present invention, the compositions H CH R24O -— CHO -I- H H - C - H herein can be free of synthetic detergents. Preferred are the mild synthetic surfactants disclosed in U.S. Pat. No. 4,673,525, Small et al., issued June 16, 1987, incorporated herein by reference.
Insoluble Alkaline Earth Metal Soaps Insoluble alkaline earth metal soaps such as calcium stearate and magnesium stearate can also be incorporated into compositions of the present invention at levels up to about 30%. These materials are particularly useful in toilet bars in which synthetic detergents are present in that they tend to reduce the relatively high solubility which such bars normally have. These alkaline earth metal soaps are not included within the term "soap" as otherwise used in this specification. The term "soap" as used herein refers to the alkali metal soaps.
Optional Components The compositions of the present invention can contain optional components such as those conventionally found in personal cleansing products. Conventional antibacterial agents can be included in the present compositions at levels of from about 0.5% to about 4%. Typical antibacterial agents which are suitable for use herein are 3,4-di and 3,4',5-tribromosalicy!a-aniIdes; 4,4'-dichloro-3-(trifluoromethyl)carbani1ide; 3,4,4'-trichlorocarbani1 -ide and mixtures of these materials. Conventional nonionic emollients can be included as additional skin conditioning agents in the compositions of the present invention at levels up to about 40%, preferably at levels of from about 1% to about 25%. Such materials include, for example, mineral oils, paraffin wax having a melting point of from about 100°F., fatty sorbitan esters (see U.S. Pat. No. 3,988,255, Seiden, issued Oct. 26, 1976, incorporated by reference herein), lanolin and lanolin derivatives, esters such as isopropyl myristate and triglycerides such as coconut oil or hydrogenated tallow.
Free fatty acid such as coconut fatty acid can be added to the compositions herein to improve the volume and quality (creami-ness) of the lather produced by the compositions herein.
Conventional perfumes, dyes and pigments can also be incorporated into compositions of the invention at levels up to about 234 2 9 3 %. Perfumes are preferably used at levels of from about 0.5% to 3% and dyes and pigments are preferably used at levels of from about 0.001% to about 0.5%.
Bar Preparation Toilet bars of the present invention can be prepared in any conventional manner. E.g., the bulky amine cationic polymer can be added to noodles of the base soap mixture containing from about 10% to about 22% moisture in an amalgamator. Any optional ingredients such as perfumes, dyes, etc., are also added to the amalgamator. The mixture is processed in the amalgamator and milled in the conventional manner under conventional conditions. It is then extruded (plodded) into logs for cutting and stamping into toilet bars.
In a method of making the bar of the present invention, the bulky amine cationic polymer is added to soap noodle and mixed in the soap mixing steps of the soap bar making process.
The soap bars of this invention preferably contain up to 20% of a synthetic surfactant. If a synthetic surfactant is included, a mild one is preferred. A mild synthetic surfactant is defined herein as one which does relatively little damage to the barrier function of the stratum corneum. The mild surfactant is preferably used at a level of 0-20%, preferably about 2-15%. The fatty acid soap and mild surfactant mixture preferably has a ratio of 2.5:1 to 37:1, preferably from 2.5:1 to 14:1, and most preferably from 6.5:1 to 14:1, soap:synthetic.
A preferred soap bar of this invention also contains from about 2% to about 17% moisturizer, preferably one selected from glycerin and free fatty acid or mixtures thereof. The more preferred bar of this invention contains at least 4% moisturizer.
Some preferred mild synthetic surfactants useful in this invention include alkyl glyceryl ether sulfonate (AGS), anionic acyl sarcosinates, methyl acyl taurates, N-acyl glutamates, alkyl glucosides, acyl isethionates, alkyl sulfosuccinate, alkyl phosphate esters, ethoxylated alkyl phosphate esters, alkyl ether sulfates, methyl glucose esters, protein condensates, mixtures of alkyl ether sulfates and alkyl amine oxides, betaines, sultaines, and mixtures thereof. Included in the surfactants are the alkyl 2342 93 ether sulfates with 1 to 12 ethoxy groups, especially ammonium and sodium lauryl ether sulfates. Alkyl chain lengths for these surfactants are C8-C22. preferably Cjo-Cis- The most preferred mild surfactant is sodium CN AGS.
The following examples are presented by way of illustration only.
EXAMPLES I AND 2 Toilet bars made using the ingredients set out in Table 2.
TABLE 2 Ex. I Ex. 2 Ingredient Parts Parts Sodium TallowateU) 32.90 32.90 Sodium Cocoate(1) 32.90 32.90 Water 9.50 9.50 Sodium Cocoglyceryl Ether Sulfonate (AGS) 8.80 8.80 Glycerin 4.00 4.00 Coconut Fatty Acid 3.80 3.80 Triclocarban 1.50 1.50 Sodium Chloride 1.20 1.20 Fragrance 1.20 1.20 Polyquaternium-7(2) 1.00 1.00 LM-200(3) 1.00 Guar-HPTC(4) - 1.00 Titanium Dioxide 0.35 0.35 Tetrasodium EDTA 0.06 0.06 BTH(5) 0.02 0.02 Mi seel 1aneous(6) * * Totals 100.00 100.00 (1) The values stated for sodium tallowate and sodium cocoate include a low level (>0.1%) of unsaponifiable materi al. (2) The trade name for Polyquaternium-7 is Meraquat 500. (3) LM-200 is a cationic cellulosic polymer comprising a bulky cocoyl amine. ? 1 /i 9 /L k c. (4) Guar HPTC is guar hydroxypropyltriammonium chloride is Jaguar C-15 (Hi-Tek). Molecular weight is about 200,000 ±75,000. (5) BHT is included in the respective perfume formulas to impart preservative/antioxidant properties both to the perfume and to the finished bar formula. (6) "Miscellaneous" includes a low level of sodium sulfate and unsulfonated alcohol which come in, e.g., as a by-product of the AGS stream.
LO In general, making procedures common to those used for conventional toilet soap bar making are employed.
Mixing/Mil 1inq Steps Polymer Addition Step Plodded soap noodles are conveyed to a continuous mixer (CM) 15 where approximately 1.0 part of cationic polymer is introduced, mixed, and plodded with the soap noodles. Uniform distribution during this addition and mixing step is important for acceptable bar feel performance. The polymer/soap noodles (generic noodles) are conveyed to milling.
Generic Hi 11inq Step Two four-roll soap mills (feed, stationary, middle, and top rolls) are used in this step. This is a split milling (two set of mills are used in parallel) process to obtain a homogeneous mix. Efficient milling is needed in this intimate mixing step. 2 5 Dry Mixing Step The generic noodles are conveyed to a second process system continuous mixer (CM) for the addition and mixing of other minors. This mix is plodded and conveyed to the third process CM. Wet Mixing Step The perfume and NaCl/sodium ethylene diamine tetra acetate (EDTA) solution are added and mixed in this wet mixing (CM) step. This finished soap formula is then plodded into soap noodles and conveyed via a transport plodder to a final milling step.
The mixture is milled using a four-roll mill, plodded, and 35 then stamped into toilet bars of any convenient size and shape. The resulting bars are tested for odor. The bars have a pH of 9.5 in a 1% aqueous solution.

Claims (13)

234293 - 12 -Odor Test Procedure Polvmer Cleaning Stock samples of polymer are cleaned by swelling the polymer with water followed by extensive aeration. These "cleaned" polymers are fairly amine odor-free. After long storage times, some of these polymers exhibited a slight, but recognizable amine odor. Bulky modified polymers required little, if any, cleansing prior to testing/evaluating. Effects Testing Procedures The general procedure followed in evaluating the effects of pH on polymer or final product odor was to place about 200 mg of the clean polymer (or a finished product) in a screw-top vial (8 dram) and then add the test solution (buffers at pH values of 7, 10, or 14). The vials are capped and the odor allowed to build up for a short amount of time. Odor is evaluated via olfactory sensing by a panel of experts. The pH buffers are commercially available buffers: pH 7 - KH2P04-Na0H pH 10 - H3BO3-KOH pH 14 - IN NaOH. TABLE 3 Odor Evaluation of Polymers and Products Under Induced Alkaline Conditions fpH -10-14) Polymer/Product Odor Evaluation JR-400 Strong amine odor Jaguar C-15 Strong amine odor LM-200 No amine odor Product of Ex. 1 No amine odor Product of Ex. 2 Strong amine odor Note: Ex. 1 product produced with LM-200 Ex. 2 product produced with Jaguar JR-400 made by Union Carbide Corporation and JAGUAR C-15 made by Hi-Tek Polymers, Inc., are outside the selected polymers of this invention. 23 4 2 9 3 -13- WhAT U'E CLAIM IS:
1. A personal cleansing composition comprising from 5% to 90% by weight of surfactant selected from the group consisting of synthetic surfactant, alkali metal soap, and mixtures thereof; and from 0.2% to 5% by weight bulky amine cationic polymer, said cationic polymer being essentially free of potential labile odoriferous amine groups; and wherein said composition has an alkaline pH of at least 7.5 in a 1% aqueous solution.
2. The personal cleansing composition of Claim 1 wherein said bulky amine group is: (POLYMER)-CR1H-CR2r3-N+r4r5r6 wherein R*, and R^ are the same or different and each is H or any other substituent and R^, R^ and Rk combine with N to form an amine with Igss odor impact than trimethylamine.;
3. The personal cleansing composition of Claim 2 wherein said cationic polymer is a cationic guar gum and wherein said composition is in a form selected from liquids, pastes and bars.;
4. The personal cleansing composition of Claim 1 wherein said cationic polymer is selected from the group consisting of :;C12H25;Guar-CH2-0-CH2-CH(OH)-CH2-N+CH3;I;CH3 ;;CH2CH2OH;I;Guar-CH2-0-CH2-CH(OH)-CH2-N+CH3;I;CH3 ; and mixtures thereof; and wherein said polymer has a molecular weight of from 50,000 to 1,000,000.;13 JULir;5;■14-;
5. Trie cati on ic weight.;personal cleansing composition of Claim polymer is present at from 0.5%;e-w p;" A.;^wjiifr£-iVi to 1 4%;9.;by;
6. The personal cleansing composition of Claim 1 wherein said cationic polymer has a molecular weight of from 1,000 to 3,000,000 and is selected from the group consisting of:;(I) cationic polysaccharides;;(II) cationic copolymers of saccharides and synthetic cationic monomers, and (III) synthetic polymers selected from the group consisting of:;(A) quaternized silicones,;(B) quaternized methacryl ates; and (IV) mixtures thereof.;
7. The personal cleansing composition of Claim 1 wherein said pH i s at 1 east 8.5.;
8. A process for preparing the personal cleansing composition of Claim 1 comprising the steps of:;(a) forming a mixture of said cationic polymer metal soap mix noodles wherein said polymer in said mixture at a level to provide from 0.2% to;5% by weight of said polymer in said said mixture containing from 6%;moisture;;(b) milling said mixture into a uniform mixture;;(c) plodding said uniform mixture;;(d) extruding said milled and plodded mixture; and;(e) stamping said extruded mixture into toilet bars.;and alkali is present composition; to 15%;'l;-1 m (993;-15-;
9. The personal cleansing composition of Claim 1 wherein said composition contains from 2% to 20% of synthetic surfactant selected from alkyl glyceryl ether sulfonates, anionic acyl sarcosinates, methyl acyl taurates, N-acyl glutamates, alkyl glucosides, acyi isethionates, alkyl sulfosuccinates, alkyl phosphate esters, ethoxylated alkyl phosphate esters, methyl glucose esters, protein condensates, mixtures of ethoxylated alkyl sulfates and alkyl amine oxides, betaines, sultaines, the alkyl ether sulfates with 1 to 12 ethoxy groups, and mixtures thereof, wherein said synthetic surfactant contains alkyl chains containing from 8 to 22 carbon atoms.;
10. The personal cleaning composition of Claim 9 wherein said composition contains from 5. to 10:.' of a Cg-C^g alkyl glyceryl ether sulfonate.;
11. A composition as claimed in any one of Claims 1 to 7, 9 and 10 substantially as hereinbefore described with reference to any example thereof.;
12. A process as claimed in Claim 8 when performed substantially as hereinbefore described with or without reference to any example thereof.;
13. A personal cleansing composition when prepared by a process as claimed in Claim 8 or Claim 12.;i MED THISDAY OF;A. J. PARKk&.SON";per . / / (;AGENTS!JOWTHE APPLICANTS;"I MAY m;'*• v.
NZ234293A 1989-06-30 1990-06-28 Personal cleansing compositions containing a surfactant and a bulky amine cationic polymer NZ234293A (en)

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AR (1) AR243596A1 (en)
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AU (1) AU620999B2 (en)
BR (1) BR9003038A (en)
CA (1) CA2019264C (en)
DE (1) DE69026651T2 (en)
DK (1) DK0405664T3 (en)
EG (1) EG19777A (en)
ES (1) ES2086362T3 (en)
GR (1) GR3019754T3 (en)
MA (1) MA21897A1 (en)
MX (1) MX173483B (en)
MY (1) MY107250A (en)
NZ (1) NZ234293A (en)
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US5154849A (en) * 1990-11-16 1992-10-13 The Procter & Gamble Company Mild skin cleansing toilet bar with silicone skin mildness/moisturizing aid
US5387675A (en) * 1993-03-10 1995-02-07 Rhone-Poulenc Specialty Chemicals Co. Modified hydrophobic cationic thickening compositions
US5849280A (en) 1996-08-06 1998-12-15 A-Veda Corporation Hair conditioning solid
US5858939A (en) * 1997-03-21 1999-01-12 Lever Brothers Company, Division Of Conopco, Inc. Method for preparing bars comprising use of separate bar adjuvant compositions comprising benefit agent and deposition polymer
ATE545660T1 (en) * 2004-08-31 2012-03-15 Hercules Inc METHOD FOR PRODUCING LOW MOLECULAR CATIONIC POLYGALACTOMANNAN WITH REDUCED ODOR
IT1391979B1 (en) * 2008-07-18 2012-02-02 Lamberti Spa MODERN GALACTOMANNAN ETHERS
JP5367494B2 (en) * 2009-08-06 2013-12-11 花王株式会社 Manufacturing method of frame kneaded soap

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US3761418A (en) * 1967-09-27 1973-09-25 Procter & Gamble Detergent compositions containing particle deposition enhancing agents
US4061602A (en) * 1976-08-03 1977-12-06 American Cyanamid Company Conditioning shampoo composition containing a cationic derivative of a natural gum (such as guar) as the active conditioning ingredient
US4234464A (en) * 1979-04-09 1980-11-18 Gaf Corporation Detergent bar composition and binder therefor
US4948576A (en) * 1983-02-18 1990-08-14 Johnson & Johnson Consumer Products, Inc. Detergent compositions
ATE103800T1 (en) * 1987-09-17 1994-04-15 Procter & Gamble LOW MOISTURE SKIN CLEANSING BAR.
MY105119A (en) * 1988-04-12 1994-08-30 Kao Corp Low irritation detergent composition.
EP0367335B1 (en) * 1988-11-02 1994-06-15 The Procter & Gamble Company Toilet bar composition containing cationic guar gum
DE3919669A1 (en) * 1989-06-16 1990-12-20 Wella Ag CLEAR HAIR AND BODY CLEANSER

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EP0405664A2 (en) 1991-01-02
ES2086362T3 (en) 1996-07-01
AR243596A1 (en) 1993-08-31
CA2019264A1 (en) 1990-12-31
BR9003038A (en) 1991-08-20
DK0405664T3 (en) 1996-08-12
GR3019754T3 (en) 1996-07-31
JPH03115210A (en) 1991-05-16
MA21897A1 (en) 1991-04-01
MX173483B (en) 1994-03-08
MY107250A (en) 1995-10-31
CA2019264C (en) 1995-07-18
AU5805590A (en) 1991-01-03
PE13191A1 (en) 1991-04-05
TR24531A (en) 1991-11-01
ATE137260T1 (en) 1996-05-15
DE69026651T2 (en) 1996-11-21
EP0405664A3 (en) 1991-01-16
JP2930671B2 (en) 1999-08-03
EG19777A (en) 1996-03-31
DE69026651D1 (en) 1996-05-30
AU620999B2 (en) 1992-02-27
EP0405664B1 (en) 1996-04-24

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