Patent Application
20180207072
The present invention relates to a stabilization mixture, i.e. a finely distributed dispersion of hydrogenated castor oil in water with anionic, amphoteric and nonionic surfactants which is suitable for stabilizing the pearlescence of surfactant agents, particularly cosmetic agents. Furthermore, the present invention relates to a cold process for producing surfactant-containing agents having a pearlescent effect, in particular cosmetic cleaning agents having a pearlescent effect, and to the use of the stabilizing mixture for stabilizing surfactant agents containing pearlescent waxes and/or pearlescent pigments containing surfactant agents.
The manufacturers of cosmetic preparations attempt to give their products an attractive, valuable and rich appearance by means of pearlescence. For modern cosmetics, pearlescent waxes, in particular of the type of the glycol monofatty and difatty acid esters, are of importance, for example, stearates, which are used, for example, for producing pearlescence in hair shampoos and shower gels. Pigments such as titanium dioxide, iron oxides or mica are also used for imparting pearlescence in cosmetic agents. In the end product, these pearlescent substances are stabilized in an anionically based matrix, and ideally in such a manner that a fine and homogeneous distribution of the pearlescent substances is present and this state is also maintained under normal storage conditions.
Commercially available pearlescent waxes have melting points above 80° C. and can therefore not be incorporated cold into aqueous formulations. The person skilled in the art is therefore generally forced to work according to a hot process in the production of surfactant agents having a pearlescent effect, i.e. to melt the waxes and to slowly crystallize it in the formulation, wherein the fineness of the crystals and thus the brilliance of the pearlescence is a function of the cooling rate. Such methods are time-consuming and energy-intensive. Furthermore, with this production method it is frequently difficult to guarantee reproducible conditions, which frequently entails fluctuations in quality. Methods for producing stabilized surfactant agents having a pearlescent effect should therefore have as few steps as possible with strong heat input.
Use of hydrogenated castor oils for stabilizing insoluble constituents in surfactant agents, wherein the hydrogenated castor oils are incorporated into the surfactant agent in a hot process is known (DE 102006032505, EP 2037877 B1). If the methods described here are applied, it entails previously described disadvantage of an additional production step using heat.
A cold process for provision of pearlescent waxes in aqueous surfactant solutions is known from DE 19921187 A1 (EP1177274 B1). However, the method requires simultaneous addition of pearlescent waxes in combination with polyolesters, which lower the melting point of the pearlescent waxes.
The subject of the present invention was to provide a composition for stabilization of pearlescent agents, such as shampoos or shower gels, wherein said composition can be mixed cold with the agent containing pearlescent substances. It was also a subject of the present invention to provide a simple method for stabilization of agents containing pearlescent substances, wherein an additional heat application is not necessary.
It has surprisingly been found that this can be achieved with an aqueous composition containing hydrogenated castor oil and a combination of anionic, nonionic and amphoteric surfactants. With the use of surfactants in specific quantities in this composition, the hydrogenated castor oil is distributed very finely. Surprisingly, a clear stabilization of surfactant agents containing pearlescent substances was observed when the stabilizing mixture according to the invention was incorporated in a cold state into a surfactant agent containing pearlescent substances.
The present invention relates to:
1. An aqueous dispersion of hydrogenated castor oil for stabilization of aqueous surfactant agents containing pearlescent waxes and/or pearlescent pigments, which, relative to its total weight, contains:
2. A dispersion according to point 1 above, containing the following relative to its total weight:
3. A dispersion according to point 1 or 2 above, wherein the dispersion does not contain a cationic surfactant.
4. A dispersion according to point 1 or 2 above, wherein the dispersion does not contain polyolester.
5. A dispersion according to one of the points above,
wherein an alkali or ammonium salt of lauryl ether sulfate with a degree of ethoxylation of 2 to 4 ethylene oxide groups or a mixture thereof is contained.
6. A dispersion according to one of the points above,
wherein one or more betaines are contained as the amphoteric surfactant (c), preferably cocamidopropyl hydroxysultains (INCI) and/or cocamidopropyl betaine (INCI).
7. A dispersion according to one of the points above,
wherein the nonionic surfactant (d) is selected from
8. A dispersion according to one of the points above, wherein the nonionic surfactant is selected from
9. A dispersion according to one of the points above, wherein the nonionic surfactant (d) is selected from, laureth-4 (INCI), PEG-7 glycerol cocoate (INCI), PEG-40 hydrogenated castor oil (INCI) and mixtures thereof.
10. A dispersion according to one of the points above, wherein the dispersion has a pH value in the range of 4.5 to 5.5.
11. A dispersion according to one of the points above, wherein the dispersion contains 40 to 90 wt. %, preferably 50 to 85 wt. % and particularly 60 to 80 wt. % water relative to its total weight.
12. A dispersion according to one of the points above, wherein the dispersion contains only water as a carrier.
13. A method for production of a stabilized surfactant-containing aqueous agent having a pearlescent effect, wherein a dispersion according to one of points 1 to 12 above is introduced to an aqueous agent containing pearlescent wax and/or pearlescent pigments in a cold process.
14. A method for producing a stabilized surfactant-containing aqueous agent having a pearlescent effect, wherein a dispersion according to one of points 1 to 12 above is introduced to a surfactant-containing aqueous agent containing anti-dandruff pigments, preferably zinc pyrithion, in a cold process.
15. A method according to point 13 or 14 above, wherein the surfactant-containing aqueous agent is a cosmetic cleaning agent, particularly a shampoo or shower gel.
16. A method according to point 13 or 14 above, wherein the surfactant-containing aqueous agent contains one or multiple components from the group of titanium dioxide, iron oxide and mice.
17. A method according to one of points 13 to 16 above, wherein the quantity of hydrogenated castor oil introduced in a stabilized surfactant-containing aqueous agent is 0.1 to 1 wt. %, preferably 0.2 to 0.5 wt. %.
18. Use of a dispersion according to one of points 1 to 12 above for stabilization of surfactant-containing aqueous agents, particularly shampoos or shower gels containing pearlescent waxes and/or pearlescent pigments.
19. Use of a dispersion according to one of points 1 to 12 above for stabilization of surfactant-containing aqueous agents, particularly shampoos or shower gels containing anti-dandruff pigments, particularly zinc pyrithion.
20. Use according to one of claim 18 or 19, wherein the proportion by weight of the dispersion according to one of points 1 or 12 of the total weight of the surfactant-containing aqueous agent is 0.5 to 10 wt. %, preferably 1 to 8 wt. % and particularly 1.5 to 6 wt. %.
The stabilization mixture according to the invention is a dispersion of hydrogenated castor oil in an aqueous phase. With the surfactants used and adherence to the specified quantities, the hydrogenate castor oil is distributed very finely in the aqueous phase. The dispersion according to the invention is often referred to hereinafter simply as a stabilization mixture.
Surprisingly, if the stabilization mixture according to the invention is mixed cold with an aqueous surfactant agent containing pearlescent substances, such as pearlescent waxes and/or pearlescent pigments, a clear stabilization of the pearlescent substances in the surfactant agent is achieved. Stabilization according to the invention is understood to means that essentially no phase separations occur in the obtained surfactant agent in conventional storage stability tests, for example at a temperature of 40 to 50° C., and no visible changes appear over extended periods at room temperature.
Aqueous surfactant agents that can be stabilized by the stabilization mixture according to the invention are understood to means, in particular, surfactant cleaning agents having pearlescence, preferably cosmetic cleaning agents such as shampoos or shower gels, as well as dishwashing agents.
An essential component of the stabilization mixture according to the invention is hydrogenated castor oil. Hydrogenated castor oil is sold, for example, under the name Cutina® HR (BASF). Hydrogenated castor oils that can be used in the present invention normally have a melting point in the range of 60 to 100° C., preferably 70 to 90° C., more preferably 80 to 90° C., particularly 85 to 88° C.
According to the invention, polyalkoxylated or polyethoxylated derivatives or addition products of hydrogenated castor oil are not encompassed by the term “hydrogenated castor oil”.
The hydrogenated castor oil is contained in the stabilization mixture according to the invention in a quantity of 1 to 25 wt. %, preferably 2.5 to 15 wt. %, more preferably 5 to 10 wt. %, relative to the total weight of the stabilization mixture in each case.
Furthermore, the stabilization mixture according to the invention contains anionic, amphoteric and nonionic surfactants as necessary components. The surfactants should be suitable for contact with the human body, particularly if they are used in end products for care and/or cleaning of the human body.
According to the invention, the following anionic surfactant substances are suitable as anionic surfactants. They are characterized by a water-solubilizing anionic group, such as a carboxylate, sulfate or sulfate group, sulfonate or phosphate group and a lipophilic alkyl group having about 8 to 30 carbon atoms. Furthermore, the molecule can contain glycol or polyglycol ether groups, ester, ether and amide groups, as well as hydroxyl groups. Examples of suitable anionic surfactants are, each in the form of sodium, potassium and ammonium salts, as well as mono-, di- and trialkanol ammonium salts having 2 to 4 carbon atoms in the alkanol group,
wherein R is a preferred linear alkyl group having 8 to 30 carbon atoms and x=0 or 1 to 12,
wherein R6 preferably denotes an aliphatic hydrocarbon radical having 8 to 30 carbon atoms, R7 for hydrogen, a radical (CH2CH2O)nR6 or X, n denotes numbers from 1 to 10 and X denotes hydrogen, an alkali or alkaline earth metal or NR8R9R10R11, with R8 to R11 denoting a C1 to C4 hydrocarbon radical independently of each other,
R12CO(AlkO)nSO3M (III)
in R12CO denotes a linear or branched, aliphatic, saturated and/or unsaturated acyl radical having 6 to 22 carbon atoms, alcohol denotes CH2CH2, CHCH3CH2 and/or CH2CHCH3, n denotes numbers from 0.5 to 5 and M denotes a cation, as described in DE-OS 197 36 906.5,
wherein R13CO denotes a linear or branched acyl radical having 6 to 22 carbon atoms, x, y and z in total denote 0 or numbers from 1 to 30, preferably 2 to 10, and X denotes an alkali or alkaline earth metal. Typical examples of monoglyceride (ether) sulfates suitable for the purposes of the invention are the reaction products of lauric acid monoglyceride, coconut fatty acid monoglyceride, palmitic acid monoglyceride, stearic acid monoglyceride, oleic acid monoglyceride and tallow fatty acid monoglyceride, and also the ethylene oxide adducts thereof sulfur trioxide or chlorosulfonic acid in the form of their sodium salts. Preferably, monoglyceride sulfates of formula (IV) are used, wherein R13CO denotes a linear acyl radical having 8 to 18 carbon atoms.
Preferred surfactants are alkyl sulfates, alkyl polyglykol ether sulfates and ether carboxylic acid salts having 10 to 18 carbon atoms in the alkyl group and up to 12 glycol ether groups in molecules of sulfosuccinic acid mono- and dialkyl esters having 8 to 18 carbon atoms in the alkyl group and sulfusuccinic acid monoalkyl polyoxyethyl esters having 8 to 18 carbon atoms in the alkyl group and 1 to 6 oxyethyl groups.
Particularly preferred anionic surfactants are the alkali metal or ammonium salts of lauryl ether sulfate having a degree of ethoxylation of 2 to 4 EO, such as the commercially available anionic surfactant with the INCI name sodium laureth sulfate.
The anionic surfactant is contained in the stabilization mixture according to the invention in a quantity of 2 to 30 wt. %, preferably 2 to 10 wt. %, more preferably 2.5 to 5 wt. % relative to the total weight of the stabilization mixture.
Amphoteric or zwitterionic surfactants are surface active compounds, which have at least one quarternary ammonium group and at least one —COO(−)— or —SO3(−) group in the molecule. Particularly suitable amphoteric surfactants are the so-called betaines such as the n-alkyl-n, n-dimethylammonium glycinates, for example coco-alkyldimethyl ammonium glycinate, n-acylaminopropyl-n, n-dimethyl ammonium glycinates, for example coco-acylaminopropyldimethyl ammonium glycinate, and 2-alkyl-3-carboxymethyl-3-hydroxyethyl imidazolines each having 8 to 18 carbon atoms in the alkyl or acyl group and coco-acylaminoethylhydroxyethyl carboxymethyl glycinate, as well as sultaines or sulfobetaines. Particularly preferred amphoteric surfactants include the compounds known by the INCI names cocamidopropyl betaine and cocamidopropyl hydroxysultaine.
According to the invention, amphoteric surfactants are also understood to mean surfactant compounds which, apart from a C8-C24 alkyl or acyl group, contain at least one free amino group and at least one COOH or —SO3H group in the molecule and are capable of forming internal salts. Examples of suitable amphoteric surfactants are N-alkylglycines, N-alkylpropionic acids, N-alkylaminobutyric acids, N-alkyliminodipropionic acids, N-hydroxyethyl-N-alkylamidopropylglycines, N-alkyltaurines, N-alkylsarcosines, 2-alkylaminopropionic acids and alkylaminoacetic acids having in each case about 8 to 24 carbon atoms in the alkyl group. Preferred amphoteric surfactants include n-coco-alkylaminopropionate, coco-acylaminoethylaminopropionate and c12-c18 acylsarcosine.
The amphoteric surfactant is contained in the stabilization mixture according to the invention in a quantity of 2 to 30 wt. %, preferably 2 to 20 wt. %, more preferably 5 to 15 wt. % relative to the total weight of the stabilization mixture.
Nonionic surfactants include, for example, at least one polyol group, a polyalkylene glycole ether group or a combination of a polyol and polyglycol ether group. Examples of such compounds include
R14CO—(OCH2CHR15)wOR16 (V)
wherein R14 denotes a linear branched, saturated and/or unsaturated acyl radical having 6 to 22 carbon atoms, R15 denotes hydrogen or methyl, R16 denotes linear or branched alkyl radicals having 1 to 4 carbon atoms and w denotes numbers from 1 to 20,
In preferred alkyl polyglycosides, R consists
Any arbitrary mono- or oligosaccharide can be used as sugar component Z. Normally, sugars having 5 or 6 carbon atoms and the corresponding oligosaccharides are used. Examples of such sugars are glucose, fructose, galactose, arabinose, ribose, xylose, allose, altrose, mannose, gulose, idose, talose and sucrose. Preferred sugar components are glucose, fructose, galactose, arabinose and sucrose; glucose is particularly preferred.
The alkyl polyglycosides used according to the invention contain an average of 1.1 to 5 sugar units. Alkyl polyglycosides having x-values from 1.1 to 2.0 are preferred. Alkyl polyglycosides in which x is 1.1 to 1.8 are more preferable.
The alkyloxylated homologs of said alkyl polyglycosides can be used according to the invention. These homologs can contain an average of up to 10 ethylene oxide and/or propylene oxide units per alkyl glycoside unit.
Preferred non-ionic surfactants have been found to be alkylene oxide addition products on saturated fatty alcohols and fatty acids having 2 to 30 moles of ethylene oxide per mole of fatty alcohol or fatty acid. Preparations with outstanding properties are also obtained if they contain fatty acid esters of ethoxylated glycerol as nonionic surfactants.
These compounds are characterized by the following parameters. The alkyl radical R contains 6 to 22 carbon atoms and can be linear or branched. Preference is given to primary linear aliphatic radicals and aliphatic radicals which are methyl-branched in the 2-position. Examples of said alkyl radicals are 1-Octyl, 1-Decyl, 1-Lauryl, 1-Myristyl, 1-Cetyl and 1-Stearyl. 1-Octyl, 1-Decyl, 1-Lauryl, 1-Myristyl are particularly preferred. With use of so-called “oxo-alcohols” as starting materials, compounds having an odd number of carbon atoms in the alkyl chain predominate.
The compounds having alkyl groups used as surfactant can be uniform substances in each case. It is normally preferable if the production of these substances starts with plant- or animal-based raw materials so that substance mixtures having different alkyl chain lengths depending on the raw material are obtained.
Examples of preferred ethoxylated fatty alcohols having an average degree of ethoxylation of 2 to 29 are Laureth-2, Oleth-2, Ceteareth-2, Laneth-2, Laureth-3, Oleth-3, Ceteareth-3, Laureth-4, Oleth-4, Ceteareth-4, Laneth-4, Laureth-5, Oleth-5, Ceteareth-5, Laneth-5, Deceth-7, Laureth-7, Oleth-7, Coceth-7, Ceteth-7, Ceteareth-7, C11-15 Pareth-7, Laureth-9, Oleth-9, Ceteareth-9, Laureth-10, Oleth-10, Beheneth-10, Ceteareth-10, Laureth-12, Ceteareth-12, Trideceth-12, Ceteth-15, Laneth-15, Ceteareth-15, Laneth-16, Ceteth-16, Oleth-16, Steareth-16, Oleth-20, Ceteth-20, Ceteareth-20, Laneth-20, Steareth-21, Ceteareth-23, Ceteareth-25, Ceteareth-27. Use of a mixture of Steareth-2 and Steareth-21 is particularly preferred.
Furthermore, preference is given to mono-, di- and tricarboxylic acid esters of saturated and/or unsaturated linear and/or branched carboxylic acids with glycerin, which can have 1 to 10, particularly 7 to 9 ethylene oxide units, such as PEG-7 glyceryl cocoate.
Additional preferred nonionic surfactants are the PEG derivatives of hydrogenated castor oil, such as the products available under the name PEG Hydrogenated Castor Oil, including PEG-30 Hydrogenated Castor Oil, PEG-33 Hydrogenated Castor Oil, PEG-35 Hydrogenated Castor Oil, PEG-36 Hydrogenated Castor Oil and PEG-40 Hydrogenated Castor Oil. According to the invention, preference is given to the use of PEG-40 Hydrogenated Castor Oil.
Among the aforementioned nonionic surfactants, compounds having the INCI names Laureth-4 (INCI), PEG-7 Glycerol Cocoate (INCI), PEG-40 Hydrogenated Castor Oil (INCI) and mixtures thereof are particularly preferred.
The nonionic surfactant is contained in the stabilization mixture according to the invention in a quantity of 2 to 30 wt. %, preferably 2 to 20 wt. %, more preferably 5 to 15 wt. % relative to the total weight of the stabilization mixture.
The stabilization mixture according to the invention can also contain a cationic surfactant. The stabilization mixture according to the invention preferably does not include a cationic surfactant.
Examples of cationic surfactants are quaternary ammonium compounds, esterquats or amidoamines.
The total quantity of surfactants is preferably contained in the stabilization mixture according to the invention in a quantity of 10 to 40 wt. %, preferably 12.5 to 35 wt. %, more preferably 15 to 30 wt. %, relative to the total weight of the stabilization mixture in each case.
The stabilization mixture according to the invention is an aqueous dispersion and, therefore, contains water as a carrier. Preference is given to dispersions containing 40 to 90 wt. %, preferably 50 to 85 wt. % and particularly 60 to 80 wt. % water, relative to the total weight. It is also preferred that no carrier other than water is included.
The stabilization mixture according to the invention is normally acidic and can contain conventional pH regulators, such as citric acid. The pH value of the stabilization mixture according to the invention is preferably in a range of 4 to 6, more preferably 4.5 to 5.5.
The stabilization mixture according to the invention contains, in addition to the aforementioned surfactants, water and the optional pH regulator, less than 10 wt. %, preferably less than 5 wt. % and particularly less than 2 wt. % of additional components.
Therefore, an additional preferred subject of the present application is an aqueous dispersion of hydrogenated castor oil for stabilization of aqueous surfactant agents containing pearlescent waxes and/or pearlescent pigments, which, relative to its total weight, contains:
and less than 10 wt. %, preferably less than 5 wt. % and particularly less than 2 wt. % of additional components.
An especially preferred subject of the present application is an aqueous dispersion of hydrogenated castor oil for stabilization of aqueous surfactant agents containing pearlescent waxes and/or pearlescent pigments, which, relative to its total weight, contains:
and less than 10 wt. %, preferably less than 5 wt. % and particularly less than 2 wt. % of additional components.
The viscosity of the stabilization mixture according to the invention is in a range of 10,000 mPas or less (Brookfield viscosimeter, 20° C., 60 s, spindle 5, 20 UpM).
The stabilization mixture according to the invention can also contain conventional additives, such as preservatives, perfumes, etc. Preferred embodiments are such that contain components in addition to hydrogenated castor oil, water, anionic surfactants, nonionic surfactants and amphoteric surfactants, a pH regulator, if applicable and a preservative, if applicable.
The stabilization mixture according to the invention can be produced according to known methods. For example a first mixture of one part water, anionic and amphoteric surfactants and, if applicable a weak acid for pH adjustment and a preservative can be prepared and heated. Then a second mixture of hydrogenated castor oil and the nonionic surfactant, which was first melted at a temperature of 90-100° C., for instance, can be added to the first mixture and homogenized at about 80 to 90° C. Finally, the remaining part of the water is added in an unheated state and the mixture is cooled while being stirred and homogenizing.
If the mixture is to be used in the same way for producing a stabilized surfactant-containing aqueous agent having a pearlescent effect, it is sufficient to carry out the cooling down to a temperature of approximately 30 to 40° C.
The present invention also relates to a method for producing a surfactant-containing aqueous agent having a pearlescent effect, wherein a stabilization mixture according to the invention is added to a surfactant-containing aqueous agent having pearlescent waxes and/or pearlescent pigments in a cold process. According to the invention, the surfactant-containing aqueous agent is preferably a cosmetic cleaning agent, particularly a shampoo or shower gen, but can also be a non-cosmetic cleaning agent, such as a dishwashing agent.
According to the invention, pearlescent waxes and/or pearlescent pigments are preferred pearlescent substances. Pearlescent waxes and pearlescent pigments are known as such. Examples of pearlescent waxes include: alkylene glycol esters, fatty acid alkanolamides, partial glycerides, esters of polyhydric, possibly hydroxy-substituted carboxylic acids, fatty alcohols, fatty acids, fatty ketones, fatty aldehydes, fatty ethers, fatty carbonates, ring-opening products of olefin epoxides and mixtures thereof.
According to the invention, however, the usable pearlescent waxes do not include hydrogenated castor oil as a component (a) of the stabilization mixture according to the invention. Pearlescent pigments are usually platelet-shaped pigments which achieve a luster effect by means of light reflection. Preferred examples are mica, titanium dioxide, iron oxide, such as Fe2O3 and Fe3O4, and combinations thereof.
Surprisingly, it has been found, that the inventive method is also suitable for producing a stabilized surfactant-containing aqueous agent having an anti-dandruff effect, wherein a stabilization mixture according to the invention is added to a surfactant-containing aqueous agent containing anti-dandruff pigments, preferably zinc pyrithion, in a cold process.
A particular advantage of the stabilization mixture according to the invention is its suitability to be mixed with surfactant-containing aqueous agent in a cold process, by means of which a stabilized pearlescent agent is obtained. This means, in particular, that the contained pearlescent substance does not aggregate and/or separate in normal storage conditions, so no visible change or phase separation occurs. Therefore, an extremely simple method is provided for production of a stable surfactant pearlescent agent by means of the present invention. As a result, disadvantages of an additional heating step and resulting quality fluctuations and reductions are avoided.
According to the invention “cold process” should be understood to mean that mixture with the surfactant pearlescent agent is normally carried out at a temperature of the stabilization mixture of 15 to 35° C. This also includes temperatures slightly above room temperature, which simplifies the processing of the mixture (i.e. pumping and dispensing compatibility). It is surprising that an even higher temperature is not necessary, for example, to melt the dispersed hydrogenated castor oil first.
In the production of a surfactant-containing aqueous agent having a pearlescent effect according to the invention, the mixture ratio of the dispersion to the cleaning agent is preferably 1:5 to 1:20, more preferably 1:5 to 1:10, particularly 1:9. In general, the mixture ratio can be selected so that an end concentration of hydrogenated castor oil in the produced surfactant-containing aqueous agent of approximately 0.1 to 1 wt. % is obtained, preferably 0.2 to 0.5 wt. %. If applicable, the stabilization mixture must first be diluted with water beforehand.
If the dispersion according to the invention and/or stabilization mixture for stabilization of surfactant-containing aqueous agents is diluted with water before mixture with the cleaning agent, the mixture ratio of the dispersion according to the invention is preferably 1:9 to 1:1, more preferably 1:5 to 1:1.
After dilution, the aqueous dispersion of hydrogenated castor oil for stabilization of aqueous surfactant agents containing pearlescent waxes and/or pearlescent pigments, which, relative to its total weight, preferably contains:
The present invention also relates to the use of the dispersion according to the invention and/or stabilization mixture for stabilization of surfactant-containing aqueous agents, particularly shampoos or shower gels containing pearlescent waxes and/or pearlescent pigments.
Furthermore, the present invention relates to the use of the dispersion according to the invention and/or stabilization mixture for stabilization of surfactant-containing aqueous agents, particularly shampoos or shower gels containing anti-dandruff pigments, particularly zinc pyrithion.
In the preferred embodiment of the inventive uses, the proportion by weight of the dispersion according to the invention and/or stabilization mixture for stabilization of surfactant-containing aqueous agents is 0.5 to 10 wt. %, preferably 1 to 8 wt. % and particularly 1.5 to 6 wt. %.
Overview Table:
The preferred stabilization mixtures according to the invention are listed below. Formulations are in wt. % and relate to the active ingredient concentration.
According to the invention “Misc” should be understood to mean essentially water. Optionally, an acid for pH adjustment or a preservative can be included. Preferably, no cationic surfactants are included under “Misc”.
1. Stabilization Mixtures
Production took place in the aqueous dispersions of hardened castor oil listed in Table 1 below. The quantity formulations indicate percent by weight, unless otherwise specified.
The production took place by preparing a first mixture from half of the water used, the anionic and amphoteric surfactant, citric acid and sodium benzoate, dissolving the mixture and heating it to 80° C. Then a second mixture of hydrogenated castor oil and the nonionic surfactant, which was first melted at a temperature of 90-100° C., for instance, was added to the first mixture, mixed at a temperature about 80 to 90° C. and homogenized under heat for 15 minutes. Then the remaining part of the water was added in an unheated state and the mixture was cooled to 35° C. and homogenized while stirring in a vacuum.
The pH value of the produced stabilization mixture was in the range of 4.5 to 5.5. The viscosity was less than 10,000 mPas (Brookfield viscosimeter, 20° C., 60 s, spindle 5, 20 UpM).
The appearance of the stabilization mixtures in examples 1 to 5 was homogeneously milky.
2. Production of Stabilized Pearlescent Shampoos
The stabilization mixtures that were obtained in examples 1 to 5, having a temperature of 35° C., were mixed with a base shampoo specified in Table 2 below having ambient temperature while stirring. The stabilizing mixtures were first diluted in the ratios specified in Table to for the mixing process.
For the purpose of comparison, the base shampoo was mixed with a corresponding amount of water and by directly introducing hydrogenated castor oil in a hot process. The mixture ratio of stabilization mixture and/or comparison mixture to base shampoo was 1:9 in each case.
The pH value of the produced stabilization mixture was in the range of 4.5 to 5.5. The viscosity was 7000 to 10,000 mPas (Brookfield viscosimeter, 20° C., 60 s, spindle 5, 20 UpM).
The stabilities of the obtained stabilized shampoos were visually evaluated after 5 days of storage at 45° C. and 50° C. The results are presented in Table 3.
Therefore, it has been demonstrated that a clear improvement of stability is achieved at increased temperatures if the stabilization mixtures according to the invention are added cold to a base shampoo.
| Number | Date | Country | Kind |
|---|---|---|---|
| 10 2015 213 478.4 | Jul 2015 | DE | national |
| Filing Document | Filing Date | Country | Kind |
|---|---|---|---|
| PCT/EP2016/059221 | 4/26/2016 | WO | 00 |
