MXPA98007242A - Bar / pasta lavatrastes transparente - Google Patents
Bar / pasta lavatrastes transparenteInfo
- Publication number
- MXPA98007242A MXPA98007242A MXPA/A/1998/007242A MX9807242A MXPA98007242A MX PA98007242 A MXPA98007242 A MX PA98007242A MX 9807242 A MX9807242 A MX 9807242A MX PA98007242 A MXPA98007242 A MX PA98007242A
- Authority
- MX
- Mexico
- Prior art keywords
- composition
- weight
- amount
- present
- carbon atoms
- Prior art date
Links
- 235000015927 pasta Nutrition 0.000 title description 2
- 239000000203 mixture Substances 0.000 claims abstract description 130
- 125000000217 alkyl group Chemical group 0.000 claims abstract description 45
- 125000004432 carbon atoms Chemical group C* 0.000 claims abstract description 38
- 235000014113 dietary fatty acids Nutrition 0.000 claims abstract description 16
- 239000000194 fatty acid Substances 0.000 claims abstract description 16
- 150000004665 fatty acids Chemical class 0.000 claims abstract description 16
- 150000001408 amides Chemical class 0.000 claims abstract description 11
- 125000000837 carbohydrate group Chemical group 0.000 claims abstract 3
- QIQXTHQIDYTFRH-UHFFFAOYSA-N Stearic acid Chemical compound CCCCCCCCCCCCCCCCCC(O)=O QIQXTHQIDYTFRH-UHFFFAOYSA-N 0.000 claims description 34
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 claims description 22
- 238000000034 method Methods 0.000 claims description 21
- 229920005862 polyol Polymers 0.000 claims description 21
- 150000003077 polyols Chemical class 0.000 claims description 21
- 235000021355 Stearic acid Nutrition 0.000 claims description 17
- 239000008117 stearic acid Substances 0.000 claims description 17
- 239000003945 anionic surfactant Substances 0.000 claims description 10
- XSQUKJJJFZCRTK-UHFFFAOYSA-N urea group Chemical group NC(=O)N XSQUKJJJFZCRTK-UHFFFAOYSA-N 0.000 claims description 10
- 150000001298 alcohols Chemical group 0.000 claims description 8
- 239000002736 nonionic surfactant Substances 0.000 claims description 8
- RTZKZFJDLAIYFH-UHFFFAOYSA-N ether Substances CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 claims description 6
- 235000000346 sugar Nutrition 0.000 claims description 6
- 239000004202 carbamide Substances 0.000 claims description 5
- SNQQPOLDUKLAAF-UHFFFAOYSA-N Nonylphenol Chemical compound CCCCCCCCCC1=CC=CC=C1O SNQQPOLDUKLAAF-UHFFFAOYSA-N 0.000 claims description 4
- IAYPIBMASNFSPL-UHFFFAOYSA-N oxane Chemical compound C1CO1 IAYPIBMASNFSPL-UHFFFAOYSA-N 0.000 claims description 4
- 229920001223 polyethylene glycol Polymers 0.000 claims description 4
- 239000002202 Polyethylene glycol Substances 0.000 claims description 3
- QAOWNCQODCNURD-UHFFFAOYSA-L sulfate Chemical compound [O-]S([O-])(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-L 0.000 claims description 3
- 238000004519 manufacturing process Methods 0.000 claims description 2
- GHNRTXCRBJQVGN-UHFFFAOYSA-N 4-dodecan-6-ylbenzenesulfonic acid Chemical group CCCCCCC(CCCCC)C1=CC=C(S(O)(=O)=O)C=C1 GHNRTXCRBJQVGN-UHFFFAOYSA-N 0.000 claims 2
- 125000001033 ether group Chemical group 0.000 claims 2
- 239000000344 soap Substances 0.000 description 22
- 235000019441 ethanol Nutrition 0.000 description 21
- 239000004094 surface-active agent Substances 0.000 description 19
- PEDCQBHIVMGVHV-UHFFFAOYSA-N glycerine Chemical compound OCC(O)CO PEDCQBHIVMGVHV-UHFFFAOYSA-N 0.000 description 14
- 238000006116 polymerization reaction Methods 0.000 description 12
- HEMHJVSKTPXQMS-UHFFFAOYSA-M sodium hydroxide Chemical compound [OH-].[Na+] HEMHJVSKTPXQMS-UHFFFAOYSA-M 0.000 description 9
- KFZMGEQAYNKOFK-UHFFFAOYSA-N iso-propanol Chemical compound CC(C)O KFZMGEQAYNKOFK-UHFFFAOYSA-N 0.000 description 8
- 238000004851 dishwashing Methods 0.000 description 7
- 235000011187 glycerol Nutrition 0.000 description 6
- 150000003871 sulfonates Chemical class 0.000 description 6
- 229960004063 Propylene glycol Drugs 0.000 description 5
- 238000009826 distribution Methods 0.000 description 5
- -1 for example Substances 0.000 description 5
- DNIAPMSPPWPWGF-UHFFFAOYSA-N propylene glycol Chemical compound CC(O)CO DNIAPMSPPWPWGF-UHFFFAOYSA-N 0.000 description 5
- 229940045714 Alkyl sulfonate alkylating agents Drugs 0.000 description 4
- 150000008052 alkyl sulfonates Chemical class 0.000 description 4
- 150000001720 carbohydrates Chemical group 0.000 description 4
- OKTJSMMVPCPJKN-UHFFFAOYSA-N carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 description 4
- LYCAIKOWRPUZTN-UHFFFAOYSA-N glycol Chemical compound OCCO LYCAIKOWRPUZTN-UHFFFAOYSA-N 0.000 description 4
- 238000005406 washing Methods 0.000 description 4
- AOMUHOFOVNGZAN-UHFFFAOYSA-N Lauroyl diethanolamide Chemical compound CCCCCCCCCCCC(=O)N(CCO)CCO AOMUHOFOVNGZAN-UHFFFAOYSA-N 0.000 description 3
- 239000002253 acid Substances 0.000 description 3
- 238000003379 elimination reaction Methods 0.000 description 3
- 238000009472 formulation Methods 0.000 description 3
- 239000011777 magnesium Substances 0.000 description 3
- 238000002156 mixing Methods 0.000 description 3
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 3
- FBPFZTCFMRRESA-FSIIMWSLSA-N D-Glucitol Natural products OC[C@H](O)[C@H](O)[C@@H](O)[C@H](O)CO FBPFZTCFMRRESA-FSIIMWSLSA-N 0.000 description 2
- FBPFZTCFMRRESA-JGWLITMVSA-N D-glucitol Chemical compound OC[C@H](O)[C@@H](O)[C@H](O)[C@H](O)CO FBPFZTCFMRRESA-JGWLITMVSA-N 0.000 description 2
- MTHSVFCYNBDYFN-UHFFFAOYSA-N Diethylene glycol Chemical compound OCCOCCO MTHSVFCYNBDYFN-UHFFFAOYSA-N 0.000 description 2
- BJHIKXHVCXFQLS-UYFOZJQFSA-N Fructose Natural products OC[C@@H](O)[C@@H](O)[C@H](O)C(=O)CO BJHIKXHVCXFQLS-UYFOZJQFSA-N 0.000 description 2
- TUNFSRHWOTWDNC-UHFFFAOYSA-N Myristic acid Chemical compound CCCCCCCCCCCCCC(O)=O TUNFSRHWOTWDNC-UHFFFAOYSA-N 0.000 description 2
- IPCSVZSSVZVIGE-UHFFFAOYSA-N Palmitic acid Chemical compound CCCCCCCCCCCCCCCC(O)=O IPCSVZSSVZVIGE-UHFFFAOYSA-N 0.000 description 2
- WQEPLUUGTLDZJY-UHFFFAOYSA-N Pentadecanoic acid Chemical compound CCCCCCCCCCCCCCC(O)=O WQEPLUUGTLDZJY-UHFFFAOYSA-N 0.000 description 2
- 150000007513 acids Chemical class 0.000 description 2
- 239000003925 fat Substances 0.000 description 2
- 235000019197 fats Nutrition 0.000 description 2
- 239000004615 ingredient Substances 0.000 description 2
- 229910052749 magnesium Inorganic materials 0.000 description 2
- OKKJLVBELUTLKV-UHFFFAOYSA-N methanol Chemical compound OC OKKJLVBELUTLKV-UHFFFAOYSA-N 0.000 description 2
- 229920000223 polyglycerol Polymers 0.000 description 2
- 229910052700 potassium Inorganic materials 0.000 description 2
- 239000011734 sodium Substances 0.000 description 2
- 229910052708 sodium Inorganic materials 0.000 description 2
- 239000000600 sorbitol Substances 0.000 description 2
- XTHPWXDJESJLNJ-UHFFFAOYSA-N sulfurochloridic acid Chemical compound OS(Cl)(=O)=O XTHPWXDJESJLNJ-UHFFFAOYSA-N 0.000 description 2
- FTTLTHNTYOVBNY-XQRVVYSFSA-N (Z)-1-chloro-2-propan-2-yloxyprop-1-ene Chemical compound CC(C)O\C(C)=C/Cl FTTLTHNTYOVBNY-XQRVVYSFSA-N 0.000 description 1
- YPFDHNVEDLHUCE-UHFFFAOYSA-N 1,3-Propanediol Chemical compound OCCCO YPFDHNVEDLHUCE-UHFFFAOYSA-N 0.000 description 1
- XXMIOPMDWAUFGU-UHFFFAOYSA-N 1,6-Hexanediol Chemical compound OCCCCCCO XXMIOPMDWAUFGU-UHFFFAOYSA-N 0.000 description 1
- BLXVTZPGEOGTGG-UHFFFAOYSA-N 2-[2-(4-nonylphenoxy)ethoxy]ethanol Chemical compound CCCCCCCCCC1=CC=C(OCCOCCO)C=C1 BLXVTZPGEOGTGG-UHFFFAOYSA-N 0.000 description 1
- WQZGKKKJIJFFOK-GASJEMHNSA-N D-Glucose Natural products OC[C@H]1OC(O)[C@H](O)[C@@H](O)[C@@H]1O WQZGKKKJIJFFOK-GASJEMHNSA-N 0.000 description 1
- CZMRCDWAGMRECN-UGDNZRGBSA-N D-sucrose Chemical compound O[C@H]1[C@H](O)[C@@H](CO)O[C@@]1(CO)O[C@@H]1[C@H](O)[C@@H](O)[C@H](O)[C@@H](CO)O1 CZMRCDWAGMRECN-UGDNZRGBSA-N 0.000 description 1
- SZXQTJUDPRGNJN-UHFFFAOYSA-N Dipropylene glycol Chemical compound OCCCOCCCO SZXQTJUDPRGNJN-UHFFFAOYSA-N 0.000 description 1
- 239000005715 Fructose Substances 0.000 description 1
- KEMQGTRYUADPNZ-UHFFFAOYSA-N Heptadecanoic acid Chemical compound CCCCCCCCCCCCCCCCC(O)=O KEMQGTRYUADPNZ-UHFFFAOYSA-N 0.000 description 1
- 235000021360 Myristic acid Nutrition 0.000 description 1
- 235000021314 Palmitic acid Nutrition 0.000 description 1
- 239000004372 Polyvinyl alcohol Substances 0.000 description 1
- 210000003491 Skin Anatomy 0.000 description 1
- CZMRCDWAGMRECN-GDQSFJPYSA-N Sucrose Natural products O([C@@H]1[C@H](O)[C@@H](O)[C@H](O)[C@H](CO)O1)[C@@]1(CO)[C@H](O)[C@@H](O)[C@@H](CO)O1 CZMRCDWAGMRECN-GDQSFJPYSA-N 0.000 description 1
- ZIBGPFATKBEMQZ-UHFFFAOYSA-N Triethylene glycol Chemical compound OCCOCCOCCO ZIBGPFATKBEMQZ-UHFFFAOYSA-N 0.000 description 1
- 239000000654 additive Substances 0.000 description 1
- 125000003158 alcohol group Chemical group 0.000 description 1
- 230000001476 alcoholic Effects 0.000 description 1
- 150000007824 aliphatic compounds Chemical class 0.000 description 1
- 125000002877 alkyl aryl group Chemical group 0.000 description 1
- 150000008055 alkyl aryl sulfonates Chemical class 0.000 description 1
- 125000005233 alkylalcohol group Chemical group 0.000 description 1
- 125000003368 amide group Chemical group 0.000 description 1
- 150000001412 amines Chemical class 0.000 description 1
- QGZKDVFQNNGYKY-UHFFFAOYSA-O ammonium Chemical compound [NH4+] QGZKDVFQNNGYKY-UHFFFAOYSA-O 0.000 description 1
- 125000003118 aryl group Chemical group 0.000 description 1
- WZEMSIKSCALWJZ-UHFFFAOYSA-O azanium;ethanol Chemical compound [NH4+].CCO.CCO WZEMSIKSCALWJZ-UHFFFAOYSA-O 0.000 description 1
- 238000009835 boiling Methods 0.000 description 1
- OYPRJOBELJOOCE-UHFFFAOYSA-N calcium Chemical compound [Ca] OYPRJOBELJOOCE-UHFFFAOYSA-N 0.000 description 1
- 239000011575 calcium Substances 0.000 description 1
- 229910052791 calcium Inorganic materials 0.000 description 1
- 229910052799 carbon Inorganic materials 0.000 description 1
- 150000007942 carboxylates Chemical class 0.000 description 1
- 150000001735 carboxylic acids Chemical class 0.000 description 1
- 239000004359 castor oil Substances 0.000 description 1
- 235000019438 castor oil Nutrition 0.000 description 1
- 238000006555 catalytic reaction Methods 0.000 description 1
- 150000001768 cations Chemical class 0.000 description 1
- 230000005591 charge neutralization Effects 0.000 description 1
- 238000006243 chemical reaction Methods 0.000 description 1
- 238000004140 cleaning Methods 0.000 description 1
- 239000003240 coconut oil Substances 0.000 description 1
- 235000019864 coconut oil Nutrition 0.000 description 1
- 150000001875 compounds Chemical class 0.000 description 1
- 230000003247 decreasing Effects 0.000 description 1
- 235000005911 diet Nutrition 0.000 description 1
- 230000037213 diet Effects 0.000 description 1
- 150000002009 diols Chemical class 0.000 description 1
- 150000002016 disaccharides Chemical class 0.000 description 1
- 238000004090 dissolution Methods 0.000 description 1
- 230000000694 effects Effects 0.000 description 1
- 229910001651 emery Inorganic materials 0.000 description 1
- 239000003623 enhancer Substances 0.000 description 1
- 230000002708 enhancing Effects 0.000 description 1
- 125000004185 ester group Chemical group 0.000 description 1
- 150000002148 esters Chemical class 0.000 description 1
- 239000006260 foam Substances 0.000 description 1
- 238000005187 foaming Methods 0.000 description 1
- 239000008103 glucose Substances 0.000 description 1
- 125000002791 glucosyl group Chemical group C1([C@H](O)[C@@H](O)[C@H](O)[C@H](O1)CO)* 0.000 description 1
- 150000002338 glycosides Chemical class 0.000 description 1
- 238000009499 grossing Methods 0.000 description 1
- 125000001183 hydrocarbyl group Chemical group 0.000 description 1
- 229910052739 hydrogen Inorganic materials 0.000 description 1
- 239000001257 hydrogen Substances 0.000 description 1
- 125000004435 hydrogen atoms Chemical class [H]* 0.000 description 1
- 238000006460 hydrolysis reaction Methods 0.000 description 1
- 230000002209 hydrophobic Effects 0.000 description 1
- 150000002500 ions Chemical class 0.000 description 1
- 238000005304 joining Methods 0.000 description 1
- FYYHWMGAXLPEAU-UHFFFAOYSA-N magnesium Chemical compound [Mg] FYYHWMGAXLPEAU-UHFFFAOYSA-N 0.000 description 1
- 239000000463 material Substances 0.000 description 1
- 230000004048 modification Effects 0.000 description 1
- 238000006011 modification reaction Methods 0.000 description 1
- 238000000199 molecular distillation Methods 0.000 description 1
- 150000002772 monosaccharides Chemical class 0.000 description 1
- PSZYNBSKGUBXEH-UHFFFAOYSA-M naphthalene-1-sulfonate Chemical class C1=CC=C2C(S(=O)(=O)[O-])=CC=CC2=C1 PSZYNBSKGUBXEH-UHFFFAOYSA-M 0.000 description 1
- 230000001264 neutralization Effects 0.000 description 1
- 238000006386 neutralization reaction Methods 0.000 description 1
- 229910000069 nitrogen hydride Inorganic materials 0.000 description 1
- 229920000847 nonoxynol Polymers 0.000 description 1
- 239000003921 oil Substances 0.000 description 1
- 235000019198 oils Nutrition 0.000 description 1
- 230000003647 oxidation Effects 0.000 description 1
- 238000007254 oxidation reaction Methods 0.000 description 1
- 239000003208 petroleum Substances 0.000 description 1
- 229920000642 polymer Polymers 0.000 description 1
- 229920002451 polyvinyl alcohol Polymers 0.000 description 1
- ZLMJMSJWJFRBEC-UHFFFAOYSA-N potassium Chemical compound [K] ZLMJMSJWJFRBEC-UHFFFAOYSA-N 0.000 description 1
- 239000011591 potassium Substances 0.000 description 1
- BDERNNFJNOPAEC-UHFFFAOYSA-N propanol Chemical compound CCCO BDERNNFJNOPAEC-UHFFFAOYSA-N 0.000 description 1
- 239000011541 reaction mixture Substances 0.000 description 1
- 150000003839 salts Chemical class 0.000 description 1
- 238000000926 separation method Methods 0.000 description 1
- KEAYESYHFKHZAL-UHFFFAOYSA-N sodium Chemical compound [Na] KEAYESYHFKHZAL-UHFFFAOYSA-N 0.000 description 1
- 239000011780 sodium chloride Substances 0.000 description 1
- 239000007787 solid Substances 0.000 description 1
- 230000003381 solubilizing Effects 0.000 description 1
- 239000000126 substance Substances 0.000 description 1
- 125000001424 substituent group Chemical group 0.000 description 1
- 239000005720 sucrose Substances 0.000 description 1
- 238000005670 sulfation reaction Methods 0.000 description 1
- 125000001273 sulfonato group Chemical group [O-]S(*)(=O)=O 0.000 description 1
- 150000003460 sulfonic acids Chemical class 0.000 description 1
- QAOWNCQODCNURD-UHFFFAOYSA-N sulfuric acid group Chemical class S(O)(O)(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-N 0.000 description 1
- 230000003655 tactile properties Effects 0.000 description 1
- 150000004072 triols Chemical class 0.000 description 1
- 239000004711 α-olefin Substances 0.000 description 1
- WQZGKKKJIJFFOK-VFUOTHLCSA-N β-D-glucose Chemical compound OC[C@H]1O[C@@H](O)[C@H](O)[C@@H](O)[C@@H]1O WQZGKKKJIJFFOK-VFUOTHLCSA-N 0.000 description 1
Abstract
The present invention relates to a transparent / translucent lava-washed composition in stick / paste form containing: (a) an alkyl polyglucoside with the general formula I. Rû (RýO) b (Z) a (I) wherein Rû is a radical monovalent organic having about 6 to about 30 carbon atoms, Rýes a divalent alkylene radical having from 2 to 4 carbon atoms, Z is a saccharide residue having 5 or 6 carbon atoms, b is a number having a value of 0 at about 12, a is a number that has a value from 1 to about 6, (b) a short chain, (c) a fatty acid, (d) an amide, and (e) a poly
Description
BAR / FASTA LAVATRA5TES TRANSPARENT
FIELD OF THE INVENTION This invention relates to transparent soap bars. More specifically, the present invention relates to transparent frets washed with soapy and foaming characteristics and
The tiansparentes soap bars are usually softer than the opara bars. These soaps, for their distinct appearance, depend on the fact that the soap is deposited from the alcoholic solution in a transparent, ultra microcrystalline form. The addition of glycerol and sugar also tends to cause soap to take this form. The effect is completely physical and depends on the conditions under which the soap crystallizes instead of the presence of alcohol or any other substance in the finished soap paste. In this way, a transparent soap made with the help of alcohol maintains its appearance after most of the alcohol has been evaporated from it. Transparent soaps vary greatly in their composition. These can be prepared by simply dissolving soap flakes in alcohol and then removing most of the alcohol. This product will not be very different in the composition of the original soap flakes. A more common manufacturing method, however, is to add alcohol and glycerol in the ratio of about 2 parts of alcohol to one of glycerol, to a hot saponified batch of semi-boiled soap until a rapidly cooled sample is clear, after which the lot is formed in the normal way. It is also possible to add sugar. The fats that are used in transparent soaps usually have bait and coconut oil. Up to about 30: castor oil is often used in fat loading, as the presence of this oil reduces the amount of alcohol, glycerol, or sugar needed to make the soap transparent. The anhydrous soap content of transparent soaps will usually be well below 50 °. There has always been a need to increase the soap and foam forming characteristics of the transparent soap bars by including various types of surfactants. However, it has been found that when a synthetic surfactant is added to a transparent soap formulation, the resulting bar is not transparent.
SUMMARY OF THE INVENTION: The present invention is directed to a rinsing composition containing: r (a) from about 2 to about 40 wt.% Of an alkyl polyglucoside of formula 1. R? (R20) b (Z) a ( 1) wherein Ri is a monovalent organic radical having from about 6 to about 30 carbon atoms; R is a divalent alkylene radical having from 2 to 4 carbon atoms; Z is a saccharide residue having 5 or 6 carbon atoms; b is a number having a value from 0 to about 12; a is a number that has a value from 1 to approximately 6; (b) from about 1 to about 10 or by weight of a short chain alcohol; (c) from about 2 to about 15 weight percent of a fatty acid; (d) from about 1 to about 20c by weight of an amide; and (e) from about 1 to about 20% by weight of a polyol, all weights being based on the weight of the composition. The present invention also provides a process for making a lava fret composition that includes the combination of the aforementioned components in the proportions described.
Description of the invention - In contrast to the operative examples, or where otherwise indicated, all numbers expressing quantities of the ingredients or reaction conditions must be understood as modified in all cases by the approximate term. alkyl polyglucosides which can be used in the compositions according to the invention have the formula 1. R (R20) b (Z) a (I) Where Ri is a monovalent organic radical having from about 6 to about 30 carbon atoms. carbon; R 1 is a divalent alkylene radical having 2 to 4 carbon atoms; Z is a saccharide residue having 5 or more carbon atoms;
6 carbon atoms; b is a number having a value from 0 to about 12; a is a number having a value from 1 to about 6. Preferred alkyl polyglycosides that can be used in the compositions according to the invention have the formula I, wherein Z is a glucose residue and b is 0. These alkyl polyglucosides are available commercially, for example, as APG®,
GLUCOPON®, or PLANTAREN® surfactants from Henkel Corporation Ambler, PA., 19002. Examples of these surfactants include, but are not limited to: 1. APG® 225 Surfactant - an alkyl polyglucoside in which the alkyl group contains from 8 to 10 carbon atoms and having an average degree of polymerization of 1.7. 2. APG® 425 Surfactant - an alkyl polyglucoside in which the alkyl group contains from 8 to 16 carbon atoms and which has an average degree of polymerization of 1.6. 3. APG® 625 Surfactant - an alkyl polyglucoside in which the alkyl group contains 12 to 16 carbon atoms and which has an average degree of polymerization of 1.6. 4. APG® 325 Surfactant - an alkyl polyglucoside in which the alkyl groups contain 9 to 11 carbon atoms and which has an average degree of polymerization of 1.6. 5. GLUCOPON® 600 Surfactant - an alkyl polyglucoside in which the alkyl groups contain from 12 to 16 carbon atoms and which have an average degree of polymerization of 1.4. 6. PLANTAREN® 2000 Surfactant -an alkyl of C "-lb polyglucoside in which the alkyl group contains from 8 to 16 carbon atoms and which has an average degree of polymerization of 1.4. 7. PLANTAREN® 1300 Surfactant - a C1- 1 alkyl polyglucoside in which the alkyl groups contain from 12 to 16 carbon atoms and which has an average degree of polymerization of 1.6. Other examples include alkyl polyglycoside surfactant compositions which are composed of mixtures of compounds of the formula I, wherein Z represents a portion derived from a reducing saccharide containing 5 or 6 carbon atoms; a is a number that has a value from 1 to approximately 6; b is 0; and R, is an alkyl radical having from 8 to 20 carbon atoms. The compositions are characterized in that they have increased surfactant properties and an HLB in the range of about 10 to about 16 and a distribution of non-Flory glycosides, which are composed of a mixture of an alkyl onoglucoside and a mixture of alkyl polyglycosides having various polymerization grades of 2 and higher in progressively decreasing amounts, in which the amount by weight of polyglucoside having a degree of polymerization of 2"or mixtures of these with the polyglucoside having a degree of polymerization of 3, predominates in relation to the amount of monoglycoside, this composition having an average degree of polymerization of about 1.8 to about 3. These compositions, also known as peak alkyl polyglucosides, can be prepared by preparing the monoglycoside from the original reaction mixture of the alkyl monoglucoside. and alkyl polyglucosides after s the elimination of alcohol. This separation can be carried out by molecular distillation and usually results in the elimination of about 70-952, by weight of alkyl monoglycoside. After the elimination of the alkyl onoglycosides, the relative distribution of the various components, mono- and polyglucosides, in the resulting product changes and the concentration in the product of the polyglucosides relative to the monoglycoside increases as well as the concentration of the individual polyglucosides with the total, that is, the fractions DP2 and DP3 in relation to the sum of all the DP fractions. These compositions are described in U.S. Patent 5,266,690, all of which is incorporated herein by reference. Other alkyl polyglucosides which can be used in the compositions according to the invention are those in which the alkyl portion contains from 6 to 18 carbon atoms; wherein [sic] and the average carbon chain length of the composition from about 9 to about 14 consists of a mixture of at least two binary components of the alkyl polyglucosides wherein each binary component is present in the mixture in relation to its average carbon chain length in an amount effective to provide the surfactant composition with the average carbon chain length of from about 9 to about 14, and wherein at least 1, or both binary components, comprises a Flory distribution of the polyglycosides derived from the acid catalyzed reaction of an alcohol containing 6-20 carbon atoms and a suitable saccharide, from which the excess alcohol has been separated. The inclusion of the alkyl polyglucosides in the formulations of the transparent soap bar containing alkanolamines, polyols, water and alkaline soaps inhibits the water oozing of polyols. A preferred alkyl polyglucoside wherein formula I, R ± is a monovalent organic radical having from about 8 to about 16 carbon atoms, b is 0 and a is a number having a value of 1.4 to 1.7. A particularly preferred alkyl polyglucoside is one in which formula I, R 'is a monovalent organic radical having from 12 to about 16 carbon atoms, b is 0 and a is a number having a value of 1.6. the amount of alkyl polyglucosides that can be used in general is in the range of about 12 to about 40% by weight, and preferably from about 5 to about 15%? in weight, based on the weight of the composition. The short chain alcohol component of the present invention can be any short chain monohydric alcohol. Suitable short chain alcohols include, but are not limited to methyl alcohol, ethyl alcohol, propyl alcohol and the like. A particularly preferred short chain alcohol is isopropyl alcohol. The amount of short chain alcohol that can be employed in the present invention is in the range of from about 1 to about 10% by weight, based on the weight of the composition. The polyol component of the soap bars according to the invention can be any aliphatic compound having two or more alcohol functionalities. These polyols include diols, triols, tetraols, etc. Examples of these polyols include, but are not limited to, ethylene glycol, 1,2-propylene glycol, 1,3-propylene glycol, diethylene glycol, dipropylene glycol, triethylene glycol, 1,6-hexylene glycol, glycerin, polyglycerols, monosaccharides. as glucose or fructose, disaccharides such as sucrose, sorbitol, and polyvinyl alcohol. Preferred polyols include 1,2-propylene glycol, glycerin, polyglycerol and sorbitol. The most preferred polyol is 1,2-propylene glycol. The amount of polyol that can be used preferably is from about 1 to about 20% by weight, and most preferably from about 7 to about 15 by weight, based on the weight of the composition. The specific amount of the polyol employed will depend on the aesthetic form of the desired composition. For example, if a clear dishwashing composition is desired, the composition will usually contain from about 8 to about 20, and from about 12 to about 16% by weight of the polyol component, based on the weight of the composition. composition. On the other hand, if a translucent washing composition is desired, the composition will usually contain from about 1 to about 10, and preferably from about 3 to about 7 or by weight of the polyol component, based on the weight of the composition. A particularly preferred polyol is CARBOWAX® 400, a linear glycol polymer available commercially from Union Carbide Corporation. The fatty acid component of the composition according to the invention can be any saturated or unsaturated carboxylic acid, branched or linear that has 8 to 30 carbon atoms or a mixture of these acids. An example of a commercial grade stearic acid, preferred is EMERSOL® 150 Stearic Acid, a registered product of Henkel Corporation, Emery Group, Cincinnati / OH., Which has an average weight percent composition of 2% myristic acid, 1% of pentadecanoic acid, 11% palmitic acid, 2% margaric acid and 83% stearic acid. The amount of the fatty acid component that can be used in the composition according to the invention is generally in the range from about 2 to about 15% by weight, and preferably from about 3 to about 8% by weight, based on the weight of the composition. A particularly preferred fatty acid component is a higher grade stearic acid containing more than 50% pure stearic acid and preferably at least 80% pure stearic acid. However, it should be noted that the specific amount of fatty acid that is employed will depend on the hardness and, therefore, the shape of the desired composition. For example, if a wash bar is desired, the composition will usually contain from at least 4% to about 15 or by weight of the fatty acid component. On the contrary, if a washing paste is desired, the composition will usually contain less than 4% by weight, and preferably from about 2.5 to about 3.5% by weight of the fatty acid component. The degree of neutralization of fatty acids in the range from at least 70% to 100%, with the most preferred range being from 90 to 100%. The fatty acids can be neutralized using any alkaline material such as, for example, sodium hydroxide. The amides which can be used in the present invention have the general formula II: useful) R5-C-N- (R4);
where R is that an alkyl group. which contains from about 8 to about 18 carbon atoms and each R4 is the same or different and is selected from the group consisting of: hydrogen, Ci-j alkyl, C?-0 and - (C¿H40-) alkanol, and mixtures thereof. The preferred amide is a diet olamide, and, more specifically, a cocodiethanolamide. It should also be noted that monoethanolamides have been found to be ineffective in the formulation of the lava fret compositions of the present invention. The amount of amine that can be used in the present invention is generally in the range of from about 1 to about 20 by weight and, preferably from about 2 to about 6% by weight, based on the weight of the composition. In a particularly preferred embodiment of the present invention, the dishwashing composition contains from about 8 to about 12% by weight of an alkyl polyglucoside of the formula 1 / wherein Ri is a monovalent organic radical having from 12 to 16 carbon atoms , from about 3 to about 5% by weight of isopropyl alcohol, from about 4 to about 60 by weight of stearic acid, from about 5 to about 10% by weight of cocodiethanolamide and from about 10 to about 14% by weight of 1, 2-propylene glycol, all weights being based on the weight of the composition. In this embodiment, the formed dishwashing composition is a transparent solid bar. However, as mentioned above, by varying the amount of the fatty acid used, in this case using less stearic acid, the composition will take the form of a paste. In the same way, by varying the amount of a polyol used, in this case using more 1,2-propylene glycol, a more translucent lava-washing composition is formed. Regardless of the desired aesthetic appearance, the amount of fatty acid employed will be in the range of from about 2 to about 15% by weight, and the amount of polyol used will be in the range of from about 1 to about 20% by weight, all of which will be weights based on the weight of the composition. It should also be noted that a bar or pasta form of the dishwashing composition of the present invention has application in institutional and industrial sectors. For example, the bar shape of the composition can be packaged in a container capable of being inverted in one direction for downward distribution. By joining a source of hot water at the end of the container's distribution, small amounts of the lava-washing composition can be melted and distributed, by gravitational drop, on the articles to be cleaned. Additional dishwashing ingredients can also be incorporated into the composition without departing from the spirit of the invention. Examples thereof include, but are not limited to, anionic surfactants, nonionic surfactants and builders. However, since the aesthetic appearance of the lavatraste composition should be in the range between transparent and translucent, the additives, such as those mentioned above, should be chosen with caution so as not to make the composition opaque. The anionic surfactants that can be employed in the composition of the present invention include linear alkyl sulfonates and ether sulphates. The sulfonate group, -SOjM bonded to an alkyl, aryl, or hydrophobic alkyl aryl is a highly effective solubilizing group. Sulfonic acids are strong acids and their salts are relatively unchanged by pH. These are stable both to oxidation and, due to the strength of the C-S bond, also to hydrolysis. These interact moderately with the hardness ions CA * and Mg - '*, significantly less than the carboxylates. The modification of the hydrophobe in the surfactants sulfonates, by the introduction of double bonds or ester or amide groups in the hydrocarbon chain or as substituents, produces surfactants that offer specific smoothing benefits. Because the introduction of the S03H function is itself inexpensive, for example, by means of fuming sulfuric acids, S0¿, S0¿, Cl¿, or NaHSO ^, the sulfonates are strongly represented among the high volume surfactants. Although representative sulfonates include alkyl aryl sulfonates, short chain lignosulfates, naphthalene sulfonates, alpha-olefin sulfonates, petroleum sulfonates and sulfonates with ester, amide or ether linkages, the present invention is directed to the use of linear or branched alkyl sulfonates (LAS ), ie linear or branched chain alkylbenzene sulphonates in their surfactant composition. Linear alkylates of these may be normal, iso (branched only at the end) or highly branched and must have at least 10 carbon atoms. Preferred linear alkyl sulfonates of the present invention contain a straight alkyl chain from about 9 to about 25 carbon atoms / more preferably from about 10 to about 13 carbon atoms, and the cation is sodium, potassium, ammonium, mono-, di- or diethanolammonium, calcium or magnesium and mixtures thereof. Suitable straight-chain alkylbenzene sulphonates include C1-? Ü alkylbenzene sulphonates. Linear alkylsulfonates will usually be employed in the composition in an amount in the range from about 5 to about 40, and preferably from 15 to 30% by weight, based on the weight of the composition. The ether sulfates which can be used are short chain alkyl sulphates characterized by the formula Ra0-S04_-X + wherein R1 is an alkyl radical of C12-16 and X is Na, K, Mg, and NH3. These can be manufactured from alkyl alcohols by sulfation with SOj or chlorosulfonic acid. The ether sulfates will usually be employed in the composition in an amount in the range of from about 1 to about 20% and, preferably, from 7 to 14% by weight, based on the weight of the composition. Suitable nonionic surfactants for use as auxiliaries in the dishwashing composition of the present invention include, for example, ethoxylated alcohols characterized by a chain length of Ca-n carbons, having from 5 to 13 moles of ethylene oxide per mole. of alcohol. A particularly preferred ethoxylated alcohol is an ethoxylated nonylphenol having 9 moles of ethylene oxide. The ethoxylated alcohols will usually be employed in the composition in an amount in the range from about 1 to about 20%, and preferably from 5 to 10%, based on the weight of the composition. Other auxiliaries that may be employed include enhancers. Particularly preferred builders include urea and / or sugar because of the improved tactile properties they impart on the dishwashing composition when in contact with human skin. These types of improvers will usually be employed in the composition in an amount in the range from about 5 about 25%, and preferably from 18 to 23% by weight, based on the weight of the composition. The present invention will be better understood from the following examples which are proposed to be illustrative only and are not intended to unduly limit the scope of the invention. Unless stated otherwise, the percentages are by weight.
Example A wash bar according to the present invention was improved with the following formulation.
Component% / weight (a) LAS 35. 5 (b) APG®, 625 * 10. 0 (c) nonylphenol (EO) and 5.25 (d) cocodiethanolamide 4. , 0 Component% / weight (e) ether sulphate 7.5 (f) 1,2-polyethylene glycol 10.0 r (g) urea 20.0 (h) stearic acid (80% pure) 4.0 (i) isopropyl alcohol 3.0 (j) NaOH 1.0 100.0
* APG®, 625 is an alkyl polyglucoside, commercially available from Henkel Corporation, Ambler, PA, in which the alkyl groups contain from 12 to 16 carbon atoms and have an average degree of polymerization of 1.6. The aforementioned surfactants were combined and heated to a temperature of about 55 ° C. The urea was then added to the mixture, with mixing until complete dissolution. The stearic acid was then added with mixing and once everything was in solution, the stearic acid then neutralized with sodium hydroxide. The isopropyl alcohol was then added with mixing. The resulting solution was then emptied into molds and allowed to harden forming a lavatories bar.
Claims (40)
1. A clear / translucent wash bowl composition in the form of stick / paste containing: (a) an alkyl polyglucoside with the general formula 1. R (R, 0) D (Z) d (I) wherein Ri is a monovalent organic radical having from about 6 to about 30 carbon atoms; R is a divalent alkylene radical having from 2 to 4 carbon atoms; Z is a saccharide residue having 5 or 6 carbon atoms; b is a number having a value from 0 to about 12; a is a number that has a value from 1 to approximately 6; (b) a short chain alcohol; (c) a fatty acid; (d) an amide; and (e) a polyol.
2. The composition of claim 1, wherein in the formula I Rx is a monovalent organic radical having from about 8 about 16 carbon atoms, b is 0 and a is a number having a value of about 1.6.
The composition of claim 1, wherein the alkyl polyglucoside is present in the composition in an amount of about 2 to about 40% by weight, based on the weight of the composition.
The composition of claim 1, wherein the short chain alcohol is present in the composition in an amount of about 1 to about 10% by weight, based on the weight of the composition.
The composition of claim 1, wherein the fatty acid is stearic acid.
6. The composition of claim 5, wherein the stearic acid is more than 50o pure.
The composition of claim 1, wherein the stearic acid is present in an amount from about 2 to about 15% by weight, based on the weight of the composition.
The composition of claim 1, wherein the amide is a diethanolamide.
The composition of claim 1, wherein the amide is present in the composition in an amount from about 1 to about 20% by weight, based on the weight of the composition.
10. The composition of claim 1, wherein the polyol is a polyethylene glycol.
The composition of claim 1, wherein the polyol is present in the composition in an amount from about 1 to about 20% by weight, based on the weight of the composition.
12. The composition of claim 1 further contains an auxiliary selected from the group consisting of an anionic surfactant, a nonionic surfactant, an improver and mixtures thereof.
The composition of claim 12, wherein the anionic surfactant is an alkylbenzene sulfonate.
The composition of claim 12, wherein the anionic surfactant is an ether sulfate.
15. The composition of claim 12 / wherein the anionic surfactant is present in the composition in an amount from about 3 to about 40% by weight, based on the weight of the composition.
16. The composition of claim 12, wherein the nonionic surfactant is an ethoxylated alcohol.
The composition of claim 16, wherein the ethoxylated alcohol is a nonylphenol having 9 moles of ethylene oxide.
The composition of claim 12, wherein the nonionic surfactant is present in the composition in an amount of from about 1 to about 20% by weight, based on the weight of the composition.
The composition of claim 12, wherein the improver is selected from the group consisting of urea, sugar and mixtures thereof.
The composition of claim 12, wherein the improver is present in the composition in an amount of from about 5 to about 25% by weight, based on the weight of the composition.
21. A process for manufacturing a transparent / translucent lava-wash composition in the form of a stick / paste which consists of combining: (a) an alkyl polyglucoside with the general formula I. R (R), (Z) "( I) wherein R- is a monovalent organic radical having from about 6 to about 30 carbon atoms; R is a divalent alkylene radical having from 2 to 4 carbon atoms; Z is a saccharide residue having 5 or 6 carbon atoms; b is a number having a value from 0 to about 12; a is a number that has a value from 1 to approximately 6; (b) a short chain alcohol; (c) a fatty acid; (d) an amide; and (e) a polyol.
22. The process of claim 21, wherein in the formula I Ri is a monovalent organic radical having about 8 about 16 carbon atoms, b is O and a is a number having a value of about 1.6.
23. The process of claim 21 / wherein the alkyl polyglucoside is present in the composition in an amount of about 2 to about 40% by weight, based on the weight of the composition.
The process of claim 21, wherein the short chain alcohol is present in the composition in an amount of about 1 to about 10% by weight, based on the weight of the composition.
25. The process of claim 21, wherein the fatty acid is stearic acid.
26. The process of claim 25, wherein the stearic acid is more than 50% pure.
The process of claim 21, wherein the stearic acid is present in an amount from about 2 to 15% by weight, based on the weight of the composition.
28. The process of claim 21, wherein the amide is a diethanolamide.
29. The process of claim 21, wherein the amide is present in the composition in an amount from about 1 to about 20% by weight, based on the weight of the composition.
30. The process of claim 21, wherein the polyol is a polyethylene glycol.
31. The process of claim 21, wherein the polyol is present in the composition in an amount from about 1 to about 20% by weight, based on the weight of the composition.
32. The process of claim 21 further contains an auxiliary selected from the group consisting of an anionic surfactant, a nonionic surfactant, an improver, and mixtures thereof.
33. The process of claim 32, wherein the anionic surfactant is an alkylbenzene sulfonate.
34. The process of claim 32, wherein the anionic surfactant is ether sulfate.
35. The process of claim 32, wherein the anionic surfactant is present in the composition in an amount from about 3 to about 40% by weight, based on the weight of the composition.
36. The process of claim 32, wherein the nonionic surfactant is an ethoxylated alcohol.
37. The process of claim 36, wherein the ethoxylated alcohol is a nonylphenol containing 9 moles of ethylene oxide.
38. The process of claim 32, wherein the nonionic surfactant is present in the composition in an amount from about 1 to about 0% by weight, based on the weight of the composition.
39. The process of claim 32, wherein the improver is selected from the group consisting of urea, sugar and mixtures thereof. -
40. The process of claim 32, wherein the improver is present in the composition in an amount from about 5 to about 25% by weight, based on the weight of the composition.
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
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US613574 | 1996-03-11 |
Publications (1)
Publication Number | Publication Date |
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MXPA98007242A true MXPA98007242A (en) | 1999-04-06 |
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