CA2095351C - Shaped solid made with a rigid, interlocking mesh of neutralized carboxylic acid - Google Patents
Shaped solid made with a rigid, interlocking mesh of neutralized carboxylic acidInfo
- Publication number
- CA2095351C CA2095351C CA002095351A CA2095351A CA2095351C CA 2095351 C CA2095351 C CA 2095351C CA 002095351 A CA002095351 A CA 002095351A CA 2095351 A CA2095351 A CA 2095351A CA 2095351 C CA2095351 C CA 2095351C
- Authority
- CA
- Canada
- Prior art keywords
- bar
- alkyl
- soap
- sodium
- water
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Expired - Fee Related
Links
- 150000001732 carboxylic acid derivatives Chemical class 0.000 title claims abstract description 30
- 239000007787 solid Substances 0.000 title abstract description 31
- 239000000344 soap Substances 0.000 claims abstract description 150
- 239000011734 sodium Substances 0.000 claims abstract description 110
- 229910052708 sodium Inorganic materials 0.000 claims abstract description 105
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 claims abstract description 88
- DGAQECJNVWCQMB-PUAWFVPOSA-M Ilexoside XXIX Chemical compound C[C@@H]1CC[C@@]2(CC[C@@]3(C(=CC[C@H]4[C@]3(CC[C@@H]5[C@@]4(CC[C@@H](C5(C)C)OS(=O)(=O)[O-])C)C)[C@@H]2[C@]1(C)O)C)C(=O)O[C@H]6[C@@H]([C@H]([C@@H]([C@H](O6)CO)O)O)O.[Na+] DGAQECJNVWCQMB-PUAWFVPOSA-M 0.000 claims abstract description 83
- -1 sodium fatty acid Chemical class 0.000 claims description 108
- 239000000203 mixture Substances 0.000 claims description 85
- 239000004094 surface-active agent Substances 0.000 claims description 74
- 125000000217 alkyl group Chemical group 0.000 claims description 63
- 235000014113 dietary fatty acids Nutrition 0.000 claims description 39
- 239000000194 fatty acid Substances 0.000 claims description 39
- 229930195729 fatty acid Natural products 0.000 claims description 39
- DNIAPMSPPWPWGF-UHFFFAOYSA-N Propylene glycol Chemical compound CC(O)CO DNIAPMSPPWPWGF-UHFFFAOYSA-N 0.000 claims description 31
- 239000012071 phase Substances 0.000 claims description 27
- 150000003839 salts Chemical class 0.000 claims description 26
- 239000004615 ingredient Substances 0.000 claims description 24
- 229920006395 saturated elastomer Polymers 0.000 claims description 22
- 239000001993 wax Substances 0.000 claims description 21
- 239000013078 crystal Substances 0.000 claims description 20
- 239000000523 sample Substances 0.000 claims description 20
- XSQUKJJJFZCRTK-UHFFFAOYSA-N Urea Chemical compound NC(N)=O XSQUKJJJFZCRTK-UHFFFAOYSA-N 0.000 claims description 18
- 239000012188 paraffin wax Substances 0.000 claims description 18
- PEDCQBHIVMGVHV-UHFFFAOYSA-N Glycerine Chemical compound OCC(O)CO PEDCQBHIVMGVHV-UHFFFAOYSA-N 0.000 claims description 17
- 125000004432 carbon atom Chemical group C* 0.000 claims description 17
- 239000008346 aqueous phase Substances 0.000 claims description 15
- 229910052744 lithium Inorganic materials 0.000 claims description 13
- 239000000463 material Substances 0.000 claims description 13
- 235000019271 petrolatum Nutrition 0.000 claims description 13
- WHXSMMKQMYFTQS-UHFFFAOYSA-N Lithium Chemical compound [Li] WHXSMMKQMYFTQS-UHFFFAOYSA-N 0.000 claims description 12
- 230000035515 penetration Effects 0.000 claims description 11
- GSEJCLTVZPLZKY-UHFFFAOYSA-O triethanolammonium Chemical compound OCC[NH+](CCO)CCO GSEJCLTVZPLZKY-UHFFFAOYSA-O 0.000 claims description 11
- 239000004264 Petrolatum Substances 0.000 claims description 10
- ZLMJMSJWJFRBEC-UHFFFAOYSA-N Potassium Chemical compound [K] ZLMJMSJWJFRBEC-UHFFFAOYSA-N 0.000 claims description 10
- 150000008051 alkyl sulfates Chemical class 0.000 claims description 10
- 239000011368 organic material Substances 0.000 claims description 10
- 229940066842 petrolatum Drugs 0.000 claims description 10
- 229910052700 potassium Inorganic materials 0.000 claims description 10
- 239000011591 potassium Substances 0.000 claims description 10
- QAOWNCQODCNURD-UHFFFAOYSA-L Sulfate Chemical compound [O-]S([O-])(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-L 0.000 claims description 9
- 239000004202 carbamide Substances 0.000 claims description 9
- 238000002844 melting Methods 0.000 claims description 9
- 230000008018 melting Effects 0.000 claims description 9
- 229920005862 polyol Polymers 0.000 claims description 9
- 150000003077 polyols Chemical class 0.000 claims description 9
- 150000003871 sulfonates Chemical class 0.000 claims description 9
- OYPRJOBELJOOCE-UHFFFAOYSA-N Calcium Chemical compound [Ca] OYPRJOBELJOOCE-UHFFFAOYSA-N 0.000 claims description 8
- FYYHWMGAXLPEAU-UHFFFAOYSA-N Magnesium Chemical compound [Mg] FYYHWMGAXLPEAU-UHFFFAOYSA-N 0.000 claims description 8
- OFOBLEOULBTSOW-UHFFFAOYSA-N Malonic acid Chemical compound OC(=O)CC(O)=O OFOBLEOULBTSOW-UHFFFAOYSA-N 0.000 claims description 8
- CZMRCDWAGMRECN-UGDNZRGBSA-N 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 claims description 8
- 229930006000 Sucrose Natural products 0.000 claims description 8
- 150000003973 alkyl amines Chemical class 0.000 claims description 8
- 235000011187 glycerol Nutrition 0.000 claims description 8
- 239000011777 magnesium Substances 0.000 claims description 8
- 229910052749 magnesium Inorganic materials 0.000 claims description 8
- 239000004200 microcrystalline wax Substances 0.000 claims description 8
- 235000019808 microcrystalline wax Nutrition 0.000 claims description 8
- 239000005720 sucrose Substances 0.000 claims description 8
- 235000000346 sugar Nutrition 0.000 claims description 8
- 150000003626 triacylglycerols Chemical class 0.000 claims description 8
- 239000011575 calcium Substances 0.000 claims description 7
- 229910052791 calcium Inorganic materials 0.000 claims description 7
- HNPSIPDUKPIQMN-UHFFFAOYSA-N dioxosilane;oxo(oxoalumanyloxy)alumane Chemical compound O=[Si]=O.O=[Al]O[Al]=O HNPSIPDUKPIQMN-UHFFFAOYSA-N 0.000 claims description 7
- 230000002209 hydrophobic effect Effects 0.000 claims description 7
- NLYAJNPCOHFWQQ-UHFFFAOYSA-N kaolin Chemical compound O.O.O=[Al]O[Si](=O)O[Si](=O)O[Al]=O NLYAJNPCOHFWQQ-UHFFFAOYSA-N 0.000 claims description 7
- DSEKYWAQQVUQTP-XEWMWGOFSA-N (2r,4r,4as,6as,6as,6br,8ar,12ar,14as,14bs)-2-hydroxy-4,4a,6a,6b,8a,11,11,14a-octamethyl-2,4,5,6,6a,7,8,9,10,12,12a,13,14,14b-tetradecahydro-1h-picen-3-one Chemical compound C([C@H]1[C@]2(C)CC[C@@]34C)C(C)(C)CC[C@]1(C)CC[C@]2(C)[C@H]4CC[C@@]1(C)[C@H]3C[C@@H](O)C(=O)[C@@H]1C DSEKYWAQQVUQTP-XEWMWGOFSA-N 0.000 claims description 6
- VTYYLEPIZMXCLO-UHFFFAOYSA-L Calcium carbonate Chemical compound [Ca+2].[O-]C([O-])=O VTYYLEPIZMXCLO-UHFFFAOYSA-L 0.000 claims description 6
- 229910000323 aluminium silicate Inorganic materials 0.000 claims description 6
- 239000004927 clay Substances 0.000 claims description 6
- 239000010457 zeolite Substances 0.000 claims description 6
- 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 claims description 5
- 239000004203 carnauba wax Substances 0.000 claims description 5
- 150000001768 cations Chemical class 0.000 claims description 5
- 230000009969 flowable effect Effects 0.000 claims description 5
- 102000004169 proteins and genes Human genes 0.000 claims description 5
- 108090000623 proteins and genes Proteins 0.000 claims description 5
- 239000000600 sorbitol Substances 0.000 claims description 5
- 235000010356 sorbitol Nutrition 0.000 claims description 5
- RMTFNDVZYPHUEF-XZBKPIIZSA-N 3-O-methyl-D-glucose Chemical class O=C[C@H](O)[C@@H](OC)[C@H](O)[C@H](O)CO RMTFNDVZYPHUEF-XZBKPIIZSA-N 0.000 claims description 4
- 239000005995 Aluminium silicate Substances 0.000 claims description 4
- VEXZGXHMUGYJMC-UHFFFAOYSA-M Chloride anion Chemical compound [Cl-] VEXZGXHMUGYJMC-UHFFFAOYSA-M 0.000 claims description 4
- 125000002252 acyl group Chemical group 0.000 claims description 4
- 150000004996 alkyl benzenes Chemical class 0.000 claims description 4
- 229910052782 aluminium Inorganic materials 0.000 claims description 4
- XAGFODPZIPBFFR-UHFFFAOYSA-N aluminium Chemical compound [Al] XAGFODPZIPBFFR-UHFFFAOYSA-N 0.000 claims description 4
- 235000012211 aluminium silicate Nutrition 0.000 claims description 4
- 125000001301 ethoxy group Chemical group [H]C([H])([H])C([H])([H])O* 0.000 claims description 4
- NBIIXXVUZAFLBC-UHFFFAOYSA-K phosphate Chemical compound [O-]P([O-])([O-])=O NBIIXXVUZAFLBC-UHFFFAOYSA-K 0.000 claims description 4
- 150000008163 sugars Chemical class 0.000 claims description 4
- 235000013311 vegetables Nutrition 0.000 claims description 4
- GDTSJMKGXGJFGQ-UHFFFAOYSA-N 3,7-dioxido-2,4,6,8,9-pentaoxa-1,3,5,7-tetraborabicyclo[3.3.1]nonane Chemical compound O1B([O-])OB2OB([O-])OB1O2 GDTSJMKGXGJFGQ-UHFFFAOYSA-N 0.000 claims description 3
- QGZKDVFQNNGYKY-UHFFFAOYSA-O Ammonium Chemical compound [NH4+] QGZKDVFQNNGYKY-UHFFFAOYSA-O 0.000 claims description 3
- CPELXLSAUQHCOX-UHFFFAOYSA-M Bromide Chemical compound [Br-] CPELXLSAUQHCOX-UHFFFAOYSA-M 0.000 claims description 3
- BVKZGUZCCUSVTD-UHFFFAOYSA-L Carbonate Chemical compound [O-]C([O-])=O BVKZGUZCCUSVTD-UHFFFAOYSA-L 0.000 claims description 3
- 239000004166 Lanolin Substances 0.000 claims description 3
- 241001465754 Metazoa Species 0.000 claims description 3
- 229920000388 Polyphosphate Polymers 0.000 claims description 3
- 240000000111 Saccharum officinarum Species 0.000 claims description 3
- 235000007201 Saccharum officinarum Nutrition 0.000 claims description 3
- HPTYUNKZVDYXLP-UHFFFAOYSA-N aluminum;trihydroxy(trihydroxysilyloxy)silane;hydrate Chemical compound O.[Al].[Al].O[Si](O)(O)O[Si](O)(O)O HPTYUNKZVDYXLP-UHFFFAOYSA-N 0.000 claims description 3
- 229960000892 attapulgite Drugs 0.000 claims description 3
- 235000013871 bee wax Nutrition 0.000 claims description 3
- 239000012166 beeswax Substances 0.000 claims description 3
- 239000000440 bentonite Substances 0.000 claims description 3
- 229910000278 bentonite Inorganic materials 0.000 claims description 3
- SVPXDRXYRYOSEX-UHFFFAOYSA-N bentoquatam Chemical compound O.O=[Si]=O.O=[Al]O[Al]=O SVPXDRXYRYOSEX-UHFFFAOYSA-N 0.000 claims description 3
- 229910000019 calcium carbonate Inorganic materials 0.000 claims description 3
- GUJOJGAPFQRJSV-UHFFFAOYSA-N dialuminum;dioxosilane;oxygen(2-);hydrate Chemical compound O.[O-2].[O-2].[O-2].[Al+3].[Al+3].O=[Si]=O.O=[Si]=O.O=[Si]=O.O=[Si]=O GUJOJGAPFQRJSV-UHFFFAOYSA-N 0.000 claims description 3
- XPPKVPWEQAFLFU-UHFFFAOYSA-J diphosphate(4-) Chemical compound [O-]P([O-])(=O)OP([O-])([O-])=O XPPKVPWEQAFLFU-UHFFFAOYSA-J 0.000 claims description 3
- 235000011180 diphosphates Nutrition 0.000 claims description 3
- 150000002169 ethanolamines Chemical class 0.000 claims description 3
- 229930182478 glucoside Natural products 0.000 claims description 3
- 229910052621 halloysite Inorganic materials 0.000 claims description 3
- 229910052900 illite Inorganic materials 0.000 claims description 3
- 229910052622 kaolinite Inorganic materials 0.000 claims description 3
- 235000019388 lanolin Nutrition 0.000 claims description 3
- JZMJDSHXVKJFKW-UHFFFAOYSA-M methyl sulfate(1-) Chemical compound COS([O-])(=O)=O JZMJDSHXVKJFKW-UHFFFAOYSA-M 0.000 claims description 3
- 229910052901 montmorillonite Inorganic materials 0.000 claims description 3
- VGIBGUSAECPPNB-UHFFFAOYSA-L nonaaluminum;magnesium;tripotassium;1,3-dioxido-2,4,5-trioxa-1,3-disilabicyclo[1.1.1]pentane;iron(2+);oxygen(2-);fluoride;hydroxide Chemical compound [OH-].[O-2].[O-2].[O-2].[O-2].[O-2].[F-].[Mg+2].[Al+3].[Al+3].[Al+3].[Al+3].[Al+3].[Al+3].[Al+3].[Al+3].[Al+3].[K+].[K+].[K+].[Fe+2].O1[Si]2([O-])O[Si]1([O-])O2.O1[Si]2([O-])O[Si]1([O-])O2.O1[Si]2([O-])O[Si]1([O-])O2.O1[Si]2([O-])O[Si]1([O-])O2.O1[Si]2([O-])O[Si]1([O-])O2.O1[Si]2([O-])O[Si]1([O-])O2.O1[Si]2([O-])O[Si]1([O-])O2 VGIBGUSAECPPNB-UHFFFAOYSA-L 0.000 claims description 3
- 229910052625 palygorskite Inorganic materials 0.000 claims description 3
- 239000001205 polyphosphate Substances 0.000 claims description 3
- 235000011176 polyphosphates Nutrition 0.000 claims description 3
- 239000012176 shellac wax Substances 0.000 claims description 3
- 239000000454 talc Substances 0.000 claims description 3
- 229910052623 talc Inorganic materials 0.000 claims description 3
- 238000005303 weighing Methods 0.000 claims description 3
- 125000006273 (C1-C3) alkyl group Chemical group 0.000 claims description 2
- BVKZGUZCCUSVTD-UHFFFAOYSA-M Bicarbonate Chemical compound OC([O-])=O BVKZGUZCCUSVTD-UHFFFAOYSA-M 0.000 claims description 2
- NBIIXXVUZAFLBC-UHFFFAOYSA-L Phosphate ion(2-) Chemical compound OP([O-])([O-])=O NBIIXXVUZAFLBC-UHFFFAOYSA-L 0.000 claims description 2
- ULUAUXLGCMPNKK-UHFFFAOYSA-N Sulfobutanedioic acid Chemical class OC(=O)CC(C(O)=O)S(O)(=O)=O ULUAUXLGCMPNKK-UHFFFAOYSA-N 0.000 claims description 2
- 150000001450 anions Chemical class 0.000 claims description 2
- ZXVOCOLRQJZVBW-UHFFFAOYSA-N azane;ethanol Chemical compound N.CCO ZXVOCOLRQJZVBW-UHFFFAOYSA-N 0.000 claims description 2
- 239000004204 candelilla wax Substances 0.000 claims description 2
- 235000013868 candelilla wax Nutrition 0.000 claims description 2
- 229940073532 candelilla wax Drugs 0.000 claims description 2
- 235000013869 carnauba wax Nutrition 0.000 claims description 2
- TWEMKOBYVAMCDD-UHFFFAOYSA-L disodium;dodecanedioate Chemical compound [Na+].[Na+].[O-]C(=O)CCCCCCCCCCC([O-])=O TWEMKOBYVAMCDD-UHFFFAOYSA-L 0.000 claims description 2
- IUJAMGNYPWYUPM-UHFFFAOYSA-N hentriacontane Chemical compound CCCCCCCCCCCCCCCCCCCCCCCCCCCCCCC IUJAMGNYPWYUPM-UHFFFAOYSA-N 0.000 claims description 2
- 239000002198 insoluble material Substances 0.000 claims description 2
- SUMDYPCJJOFFON-UHFFFAOYSA-N isethionic acid Chemical class OCCS(O)(=O)=O SUMDYPCJJOFFON-UHFFFAOYSA-N 0.000 claims description 2
- 229940039717 lanolin Drugs 0.000 claims description 2
- 229920005646 polycarboxylate Polymers 0.000 claims description 2
- 230000008961 swelling Effects 0.000 claims description 2
- 125000005270 trialkylamine group Chemical group 0.000 claims description 2
- 239000002023 wood Substances 0.000 claims description 2
- 150000002763 monocarboxylic acids Chemical class 0.000 claims 3
- 239000000835 fiber Substances 0.000 abstract description 17
- 239000007788 liquid Substances 0.000 abstract description 17
- 230000000630 rising effect Effects 0.000 abstract 1
- FAPWRFPIFSIZLT-UHFFFAOYSA-M Sodium chloride Chemical compound [Na+].[Cl-] FAPWRFPIFSIZLT-UHFFFAOYSA-M 0.000 description 26
- 238000000034 method Methods 0.000 description 25
- 150000004665 fatty acids Chemical class 0.000 description 20
- 230000008569 process Effects 0.000 description 19
- HEMHJVSKTPXQMS-UHFFFAOYSA-M Sodium hydroxide Chemical compound [OH-].[Na+] HEMHJVSKTPXQMS-UHFFFAOYSA-M 0.000 description 14
- 210000003491 skin Anatomy 0.000 description 13
- 239000011780 sodium chloride Substances 0.000 description 13
- WMFOQBRAJBCJND-UHFFFAOYSA-M Lithium hydroxide Chemical compound [Li+].[OH-] WMFOQBRAJBCJND-UHFFFAOYSA-M 0.000 description 11
- 229920001296 polysiloxane Polymers 0.000 description 11
- 239000000047 product Substances 0.000 description 11
- 238000012360 testing method Methods 0.000 description 11
- 235000013772 propylene glycol Nutrition 0.000 description 10
- 125000002091 cationic group Chemical group 0.000 description 9
- 235000021588 free fatty acids Nutrition 0.000 description 9
- 239000000306 component Substances 0.000 description 8
- 238000009472 formulation Methods 0.000 description 8
- 239000002304 perfume Substances 0.000 description 8
- 239000003599 detergent Substances 0.000 description 7
- 239000012530 fluid Substances 0.000 description 7
- 108700004121 sarkosyl Proteins 0.000 description 7
- KSAVQLQVUXSOCR-UHFFFAOYSA-M sodium lauroyl sarcosinate Chemical compound [Na+].CCCCCCCCCCCC(=O)N(C)CC([O-])=O KSAVQLQVUXSOCR-UHFFFAOYSA-M 0.000 description 7
- 229940045885 sodium lauroyl sarcosinate Drugs 0.000 description 7
- 244000060011 Cocos nucifera Species 0.000 description 6
- LYCAIKOWRPUZTN-UHFFFAOYSA-N Ethylene glycol Chemical compound OCCO LYCAIKOWRPUZTN-UHFFFAOYSA-N 0.000 description 6
- 229940091250 magnesium supplement Drugs 0.000 description 6
- 229940114937 microcrystalline wax Drugs 0.000 description 6
- 235000013162 Cocos nucifera Nutrition 0.000 description 5
- 238000001816 cooling Methods 0.000 description 5
- GPLRAVKSCUXZTP-UHFFFAOYSA-N diglycerol Chemical compound OCC(O)COCC(O)CO GPLRAVKSCUXZTP-UHFFFAOYSA-N 0.000 description 5
- 239000003623 enhancer Substances 0.000 description 5
- 230000000704 physical effect Effects 0.000 description 5
- 229920000642 polymer Polymers 0.000 description 5
- FSYKKLYZXJSNPZ-UHFFFAOYSA-N sarcosine Chemical compound C[NH2+]CC([O-])=O FSYKKLYZXJSNPZ-UHFFFAOYSA-N 0.000 description 5
- 239000000243 solution Substances 0.000 description 5
- QAOWNCQODCNURD-UHFFFAOYSA-N sulfuric acid Substances OS(O)(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-N 0.000 description 5
- 239000000271 synthetic detergent Substances 0.000 description 5
- 239000003760 tallow Substances 0.000 description 5
- 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 4
- 229910021536 Zeolite Inorganic materials 0.000 description 4
- 239000002253 acid Substances 0.000 description 4
- 150000001298 alcohols Chemical class 0.000 description 4
- 150000001412 amines Chemical class 0.000 description 4
- 238000000576 coating method Methods 0.000 description 4
- 229940071160 cocoate Drugs 0.000 description 4
- 150000002466 imines Chemical class 0.000 description 4
- 238000002156 mixing Methods 0.000 description 4
- 235000012149 noodles Nutrition 0.000 description 4
- IPCSVZSSVZVIGE-UHFFFAOYSA-N palmitic acid group Chemical group C(CCCCCCCCCCCCCCC)(=O)O IPCSVZSSVZVIGE-UHFFFAOYSA-N 0.000 description 4
- 229960002920 sorbitol Drugs 0.000 description 4
- KWYUFKZDYYNOTN-UHFFFAOYSA-M Potassium hydroxide Chemical compound [OH-].[K+] KWYUFKZDYYNOTN-UHFFFAOYSA-M 0.000 description 3
- 239000002585 base Substances 0.000 description 3
- 230000008901 benefit Effects 0.000 description 3
- 239000003518 caustics Substances 0.000 description 3
- 239000011248 coating agent Substances 0.000 description 3
- 239000003240 coconut oil Substances 0.000 description 3
- 235000019864 coconut oil Nutrition 0.000 description 3
- 238000002425 crystallisation Methods 0.000 description 3
- 230000008025 crystallization Effects 0.000 description 3
- 230000006378 damage Effects 0.000 description 3
- IGYPYJDGDAHIIV-UHFFFAOYSA-N dodecanoyloxymethanesulfonic acid Chemical compound CCCCCCCCCCCC(=O)OCS(O)(=O)=O IGYPYJDGDAHIIV-UHFFFAOYSA-N 0.000 description 3
- 150000002148 esters Chemical class 0.000 description 3
- 238000001125 extrusion Methods 0.000 description 3
- 235000013305 food Nutrition 0.000 description 3
- KWGKDLIKAYFUFQ-UHFFFAOYSA-M lithium chloride Chemical compound [Li+].[Cl-] KWGKDLIKAYFUFQ-UHFFFAOYSA-M 0.000 description 3
- 150000002762 monocarboxylic acid derivatives Chemical class 0.000 description 3
- TVIDDXQYHWJXFK-UHFFFAOYSA-N n-Dodecanedioic acid Natural products OC(=O)CCCCCCCCCCC(O)=O TVIDDXQYHWJXFK-UHFFFAOYSA-N 0.000 description 3
- QIQXTHQIDYTFRH-UHFFFAOYSA-N octadecanoic acid Chemical class CCCCCCCCCCCCCCCCCC(O)=O QIQXTHQIDYTFRH-UHFFFAOYSA-N 0.000 description 3
- 239000003921 oil Substances 0.000 description 3
- 235000019198 oils Nutrition 0.000 description 3
- 229920001282 polysaccharide Polymers 0.000 description 3
- 239000005017 polysaccharide Substances 0.000 description 3
- 125000001436 propyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])[H] 0.000 description 3
- ROSDSFDQCJNGOL-UHFFFAOYSA-N protonated dimethyl amine Natural products CNC ROSDSFDQCJNGOL-UHFFFAOYSA-N 0.000 description 3
- 230000008591 skin barrier function Effects 0.000 description 3
- 239000000126 substance Substances 0.000 description 3
- QTBSBXVTEAMEQO-UHFFFAOYSA-M Acetate Chemical compound CC([O-])=O QTBSBXVTEAMEQO-UHFFFAOYSA-M 0.000 description 2
- KRKNYBCHXYNGOX-UHFFFAOYSA-K Citrate Chemical compound [O-]C(=O)CC(O)(CC([O-])=O)C([O-])=O KRKNYBCHXYNGOX-UHFFFAOYSA-K 0.000 description 2
- QXNVGIXVLWOKEQ-UHFFFAOYSA-N Disodium Chemical class [Na][Na] QXNVGIXVLWOKEQ-UHFFFAOYSA-N 0.000 description 2
- 229920002907 Guar gum Polymers 0.000 description 2
- KDLHZDBZIXYQEI-UHFFFAOYSA-N Palladium Chemical compound [Pd] KDLHZDBZIXYQEI-UHFFFAOYSA-N 0.000 description 2
- 235000021314 Palmitic acid Nutrition 0.000 description 2
- 241000282372 Panthera onca Species 0.000 description 2
- PMZURENOXWZQFD-UHFFFAOYSA-L Sodium Sulfate Chemical compound [Na+].[Na+].[O-]S([O-])(=O)=O PMZURENOXWZQFD-UHFFFAOYSA-L 0.000 description 2
- 235000021355 Stearic acid Nutrition 0.000 description 2
- 150000007513 acids Chemical class 0.000 description 2
- 239000002671 adjuvant Substances 0.000 description 2
- 229910052783 alkali metal Inorganic materials 0.000 description 2
- 125000000129 anionic group Chemical group 0.000 description 2
- 239000007864 aqueous solution Substances 0.000 description 2
- 235000012216 bentonite Nutrition 0.000 description 2
- 229940092782 bentonite Drugs 0.000 description 2
- 229910021538 borax Inorganic materials 0.000 description 2
- MRUAUOIMASANKQ-UHFFFAOYSA-O carboxymethyl-[3-(dodecanoylamino)propyl]-dimethylazanium Chemical compound CCCCCCCCCCCC(=O)NCCC[N+](C)(C)CC(O)=O MRUAUOIMASANKQ-UHFFFAOYSA-O 0.000 description 2
- 230000015556 catabolic process Effects 0.000 description 2
- 238000004140 cleaning Methods 0.000 description 2
- 239000003086 colorant Substances 0.000 description 2
- 229940000425 combination drug Drugs 0.000 description 2
- 230000000052 comparative effect Effects 0.000 description 2
- 238000006731 degradation reaction Methods 0.000 description 2
- BNIILDVGGAEEIG-UHFFFAOYSA-L disodium hydrogen phosphate Chemical compound [Na+].[Na+].OP([O-])([O-])=O BNIILDVGGAEEIG-UHFFFAOYSA-L 0.000 description 2
- UQGFMSUEHSUPRD-UHFFFAOYSA-N disodium;3,7-dioxido-2,4,6,8,9-pentaoxa-1,3,5,7-tetraborabicyclo[3.3.1]nonane Chemical compound [Na+].[Na+].O1B([O-])OB2OB([O-])OB1O2 UQGFMSUEHSUPRD-UHFFFAOYSA-N 0.000 description 2
- BJVWCKXHSNBHGB-UHFFFAOYSA-L disodium;chloride;hydroxide Chemical compound [OH-].[Na+].[Na+].[Cl-] BJVWCKXHSNBHGB-UHFFFAOYSA-L 0.000 description 2
- 238000001035 drying Methods 0.000 description 2
- 230000002708 enhancing effect Effects 0.000 description 2
- SFNALCNOMXIBKG-UHFFFAOYSA-N ethylene glycol monododecyl ether Chemical compound CCCCCCCCCCCCOCCO SFNALCNOMXIBKG-UHFFFAOYSA-N 0.000 description 2
- 150000002194 fatty esters Chemical class 0.000 description 2
- 239000000945 filler Substances 0.000 description 2
- 150000004676 glycans Polymers 0.000 description 2
- 239000000665 guar gum Substances 0.000 description 2
- 235000010417 guar gum Nutrition 0.000 description 2
- 229960002154 guar gum Drugs 0.000 description 2
- 229940100463 hexyl laurate Drugs 0.000 description 2
- 150000004677 hydrates Chemical class 0.000 description 2
- 125000001183 hydrocarbyl group Chemical group 0.000 description 2
- TWNIBLMWSKIRAT-VFUOTHLCSA-N levoglucosan Chemical group O[C@@H]1[C@@H](O)[C@H](O)[C@H]2CO[C@@H]1O2 TWNIBLMWSKIRAT-VFUOTHLCSA-N 0.000 description 2
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 description 2
- 150000007522 mineralic acids Chemical class 0.000 description 2
- 229940105132 myristate Drugs 0.000 description 2
- 150000007524 organic acids Chemical class 0.000 description 2
- 235000005985 organic acids Nutrition 0.000 description 2
- 239000003346 palm kernel oil Substances 0.000 description 2
- 235000019865 palm kernel oil Nutrition 0.000 description 2
- JYVLIDXNZAXMDK-UHFFFAOYSA-N pentan-2-ol Chemical compound CCCC(C)O JYVLIDXNZAXMDK-UHFFFAOYSA-N 0.000 description 2
- 150000003014 phosphoric acid esters Chemical class 0.000 description 2
- 229920001281 polyalkylene Polymers 0.000 description 2
- 150000004804 polysaccharides Polymers 0.000 description 2
- 159000000001 potassium salts Chemical class 0.000 description 2
- 239000002243 precursor Substances 0.000 description 2
- 239000003755 preservative agent Substances 0.000 description 2
- 229940048084 pyrophosphate Drugs 0.000 description 2
- 230000009467 reduction Effects 0.000 description 2
- FQENQNTWSFEDLI-UHFFFAOYSA-J sodium diphosphate Chemical compound [Na+].[Na+].[Na+].[Na+].[O-]P([O-])(=O)OP([O-])([O-])=O FQENQNTWSFEDLI-UHFFFAOYSA-J 0.000 description 2
- 229940045870 sodium palmitate Drugs 0.000 description 2
- 229940048086 sodium pyrophosphate Drugs 0.000 description 2
- 159000000000 sodium salts Chemical class 0.000 description 2
- 229910052938 sodium sulfate Inorganic materials 0.000 description 2
- 235000011152 sodium sulphate Nutrition 0.000 description 2
- 239000004328 sodium tetraborate Substances 0.000 description 2
- 235000010339 sodium tetraborate Nutrition 0.000 description 2
- ZUFONQSOSYEWCN-UHFFFAOYSA-M sodium;2-(methylamino)acetate Chemical compound [Na+].CNCC([O-])=O ZUFONQSOSYEWCN-UHFFFAOYSA-M 0.000 description 2
- GGXKEBACDBNFAF-UHFFFAOYSA-M sodium;hexadecanoate Chemical compound [Na+].CCCCCCCCCCCCCCCC([O-])=O GGXKEBACDBNFAF-UHFFFAOYSA-M 0.000 description 2
- 239000007779 soft material Substances 0.000 description 2
- 239000002904 solvent Substances 0.000 description 2
- 239000003381 stabilizer Substances 0.000 description 2
- 125000004079 stearyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 description 2
- 238000003756 stirring Methods 0.000 description 2
- 150000005846 sugar alcohols Polymers 0.000 description 2
- 125000000020 sulfo group Chemical group O=S(=O)([*])O[H] 0.000 description 2
- 229920001059 synthetic polymer Polymers 0.000 description 2
- TUNFSRHWOTWDNC-UHFFFAOYSA-N tetradecanoic acid Chemical compound CCCCCCCCCCCCCC(O)=O TUNFSRHWOTWDNC-UHFFFAOYSA-N 0.000 description 2
- 235000019818 tetrasodium diphosphate Nutrition 0.000 description 2
- 239000001577 tetrasodium phosphonato phosphate Substances 0.000 description 2
- 239000011800 void material Substances 0.000 description 2
- BTANRVKWQNVYAZ-SCSAIBSYSA-N (2R)-butan-2-ol Chemical compound CC[C@@H](C)O BTANRVKWQNVYAZ-SCSAIBSYSA-N 0.000 description 1
- OMDQUFIYNPYJFM-XKDAHURESA-N (2r,3r,4s,5r,6s)-2-(hydroxymethyl)-6-[[(2r,3s,4r,5s,6r)-4,5,6-trihydroxy-3-[(2s,3s,4s,5s,6r)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyoxan-2-yl]methoxy]oxane-3,4,5-triol Chemical group O[C@@H]1[C@@H](O)[C@@H](O)[C@@H](CO)O[C@@H]1OC[C@@H]1[C@@H](O[C@H]2[C@H]([C@@H](O)[C@H](O)[C@@H](CO)O2)O)[C@H](O)[C@H](O)[C@H](O)O1 OMDQUFIYNPYJFM-XKDAHURESA-N 0.000 description 1
- 125000004178 (C1-C4) alkyl group Chemical group 0.000 description 1
- HZAXFHJVJLSVMW-UHFFFAOYSA-N 2-Aminoethan-1-ol Chemical compound NCCO HZAXFHJVJLSVMW-UHFFFAOYSA-N 0.000 description 1
- LMVGXBRDRZOPHA-UHFFFAOYSA-N 2-[dimethyl-[3-(16-methylheptadecanoylamino)propyl]azaniumyl]acetate Chemical compound CC(C)CCCCCCCCCCCCCCC(=O)NCCC[N+](C)(C)CC([O-])=O LMVGXBRDRZOPHA-UHFFFAOYSA-N 0.000 description 1
- JCBPETKZIGVZRE-UHFFFAOYSA-N 2-aminobutan-1-ol Chemical compound CCC(N)CO JCBPETKZIGVZRE-UHFFFAOYSA-N 0.000 description 1
- 125000000954 2-hydroxyethyl group Chemical group [H]C([*])([H])C([H])([H])O[H] 0.000 description 1
- WTKWFNIIIXNTDO-UHFFFAOYSA-N 3-isocyanato-5-methyl-2-(trifluoromethyl)furan Chemical compound CC1=CC(N=C=O)=C(C(F)(F)F)O1 WTKWFNIIIXNTDO-UHFFFAOYSA-N 0.000 description 1
- GUBGYTABKSRVRQ-XLOQQCSPSA-N Alpha-Lactose Chemical compound O[C@@H]1[C@@H](O)[C@@H](O)[C@@H](CO)O[C@H]1O[C@@H]1[C@@H](CO)O[C@H](O)[C@H](O)[C@H]1O GUBGYTABKSRVRQ-XLOQQCSPSA-N 0.000 description 1
- 102100025981 Aminoacylase-1 Human genes 0.000 description 1
- KWIUHFFTVRNATP-UHFFFAOYSA-N Betaine Natural products C[N+](C)(C)CC([O-])=O KWIUHFFTVRNATP-UHFFFAOYSA-N 0.000 description 1
- LSNNMFCWUKXFEE-UHFFFAOYSA-M Bisulfite Chemical compound OS([O-])=O LSNNMFCWUKXFEE-UHFFFAOYSA-M 0.000 description 1
- 239000004215 Carbon black (E152) Substances 0.000 description 1
- 229920013683 Celanese Polymers 0.000 description 1
- 244000180278 Copernicia prunifera Species 0.000 description 1
- 235000010919 Copernicia prunifera Nutrition 0.000 description 1
- 239000004375 Dextrin Substances 0.000 description 1
- 229920001353 Dextrin Polymers 0.000 description 1
- KCXVZYZYPLLWCC-UHFFFAOYSA-N EDTA Chemical compound OC(=O)CN(CC(O)=O)CCN(CC(O)=O)CC(O)=O KCXVZYZYPLLWCC-UHFFFAOYSA-N 0.000 description 1
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 1
- 241001553290 Euphorbia antisyphilitica Species 0.000 description 1
- BDAGIHXWWSANSR-UHFFFAOYSA-M Formate Chemical compound [O-]C=O BDAGIHXWWSANSR-UHFFFAOYSA-M 0.000 description 1
- WQZGKKKJIJFFOK-GASJEMHNSA-N Glucose Natural products OC[C@H]1OC(O)[C@H](O)[C@@H](O)[C@@H]1O WQZGKKKJIJFFOK-GASJEMHNSA-N 0.000 description 1
- CMBYOWLFQAFZCP-UHFFFAOYSA-N Hexyl dodecanoate Chemical compound CCCCCCCCCCCC(=O)OCCCCCC CMBYOWLFQAFZCP-UHFFFAOYSA-N 0.000 description 1
- 101000720039 Homo sapiens Aminoacylase-1 Proteins 0.000 description 1
- 102000011782 Keratins Human genes 0.000 description 1
- 108010076876 Keratins Proteins 0.000 description 1
- GUBGYTABKSRVRQ-QKKXKWKRSA-N Lactose Natural products OC[C@H]1O[C@@H](O[C@H]2[C@H](O)[C@@H](O)C(O)O[C@@H]2CO)[C@H](O)[C@@H](O)[C@H]1O GUBGYTABKSRVRQ-QKKXKWKRSA-N 0.000 description 1
- 239000004909 Moisturizer Substances 0.000 description 1
- 235000021360 Myristic acid Nutrition 0.000 description 1
- KWIUHFFTVRNATP-UHFFFAOYSA-O N,N,N-trimethylglycinium Chemical compound C[N+](C)(C)CC(O)=O KWIUHFFTVRNATP-UHFFFAOYSA-O 0.000 description 1
- 229910000503 Na-aluminosilicate Inorganic materials 0.000 description 1
- 244000021150 Orbignya martiana Species 0.000 description 1
- 235000014643 Orbignya martiana Nutrition 0.000 description 1
- 229910019142 PO4 Inorganic materials 0.000 description 1
- 235000019482 Palm oil Nutrition 0.000 description 1
- 241000269799 Perca fluviatilis Species 0.000 description 1
- 239000004698 Polyethylene Substances 0.000 description 1
- MUPFEKGTMRGPLJ-RMMQSMQOSA-N Raffinose Natural products O(C[C@H]1[C@@H](O)[C@H](O)[C@@H](O)[C@@H](O[C@@]2(CO)[C@H](O)[C@@H](O)[C@@H](CO)O2)O1)[C@@H]1[C@H](O)[C@@H](O)[C@@H](O)[C@@H](CO)O1 MUPFEKGTMRGPLJ-RMMQSMQOSA-N 0.000 description 1
- YTALAFHOXCJQNA-UHFFFAOYSA-N S(=O)(=O)(O)C(C(=O)O)CCCCCCCCCC.[Na] Chemical compound S(=O)(=O)(O)C(C(=O)O)CCCCCCCCCC.[Na] YTALAFHOXCJQNA-UHFFFAOYSA-N 0.000 description 1
- UEJGVJQWMFKMHU-UHFFFAOYSA-L S(=O)(=O)([O-])[O-].C(CCCCCCCCCCCCC)(=O)C(CO)O.[K+].[K+] Chemical compound S(=O)(=O)([O-])[O-].C(CCCCCCCCCCCCC)(=O)C(CO)O.[K+].[K+] UEJGVJQWMFKMHU-UHFFFAOYSA-L 0.000 description 1
- BQCADISMDOOEFD-UHFFFAOYSA-N Silver Chemical compound [Ag] BQCADISMDOOEFD-UHFFFAOYSA-N 0.000 description 1
- VMHLLURERBWHNL-UHFFFAOYSA-M Sodium acetate Chemical compound [Na+].CC([O-])=O VMHLLURERBWHNL-UHFFFAOYSA-M 0.000 description 1
- DBMJMQXJHONAFJ-UHFFFAOYSA-M Sodium laurylsulphate Chemical compound [Na+].CCCCCCCCCCCCOS([O-])(=O)=O DBMJMQXJHONAFJ-UHFFFAOYSA-M 0.000 description 1
- UQZIYBXSHAGNOE-USOSMYMVSA-N Stachyose Natural products O(C[C@H]1[C@@H](O)[C@H](O)[C@H](O)[C@@H](O[C@@]2(CO)[C@H](O)[C@@H](O)[C@@H](CO)O2)O1)[C@@H]1[C@H](O)[C@@H](O)[C@@H](O)[C@H](CO[C@@H]2[C@@H](O)[C@@H](O)[C@@H](O)[C@H](CO)O2)O1 UQZIYBXSHAGNOE-USOSMYMVSA-N 0.000 description 1
- GSEJCLTVZPLZKY-UHFFFAOYSA-N Triethanolamine Chemical compound OCCN(CCO)CCO GSEJCLTVZPLZKY-UHFFFAOYSA-N 0.000 description 1
- MUPFEKGTMRGPLJ-UHFFFAOYSA-N UNPD196149 Natural products OC1C(O)C(CO)OC1(CO)OC1C(O)C(O)C(O)C(COC2C(C(O)C(O)C(CO)O2)O)O1 MUPFEKGTMRGPLJ-UHFFFAOYSA-N 0.000 description 1
- 239000000853 adhesive Substances 0.000 description 1
- 230000001070 adhesive effect Effects 0.000 description 1
- 238000005273 aeration Methods 0.000 description 1
- 150000001340 alkali metals Chemical class 0.000 description 1
- 150000005215 alkyl ethers Chemical class 0.000 description 1
- 125000002947 alkylene group Chemical group 0.000 description 1
- 125000003368 amide group Chemical group 0.000 description 1
- 150000003863 ammonium salts Chemical class 0.000 description 1
- 239000002280 amphoteric surfactant Substances 0.000 description 1
- 239000012164 animal wax Substances 0.000 description 1
- 239000003945 anionic surfactant Substances 0.000 description 1
- 230000000844 anti-bacterial effect Effects 0.000 description 1
- 229940088710 antibiotic agent Drugs 0.000 description 1
- 230000004888 barrier function Effects 0.000 description 1
- WQZGKKKJIJFFOK-VFUOTHLCSA-N beta-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
- 229960003237 betaine Drugs 0.000 description 1
- 230000015572 biosynthetic process Effects 0.000 description 1
- 239000011449 brick Substances 0.000 description 1
- 239000000920 calcium hydroxide Substances 0.000 description 1
- 229910001861 calcium hydroxide Inorganic materials 0.000 description 1
- 150000007942 carboxylates Chemical class 0.000 description 1
- 150000001735 carboxylic acids Chemical class 0.000 description 1
- 229940082483 carnauba wax Drugs 0.000 description 1
- 229940081733 cetearyl alcohol Drugs 0.000 description 1
- 230000008859 change Effects 0.000 description 1
- 239000007795 chemical reaction product Substances 0.000 description 1
- 239000003795 chemical substances by application Substances 0.000 description 1
- 150000003841 chloride salts Chemical class 0.000 description 1
- 230000003750 conditioning effect Effects 0.000 description 1
- 239000000470 constituent Substances 0.000 description 1
- 230000002844 continuous effect Effects 0.000 description 1
- 230000018044 dehydration Effects 0.000 description 1
- 238000006297 dehydration reaction Methods 0.000 description 1
- 230000001419 dependent effect Effects 0.000 description 1
- 235000019425 dextrin Nutrition 0.000 description 1
- 239000008121 dextrose Substances 0.000 description 1
- ZBCBWPMODOFKDW-UHFFFAOYSA-N diethanolamine Chemical compound OCCNCCO ZBCBWPMODOFKDW-UHFFFAOYSA-N 0.000 description 1
- 150000002016 disaccharides Chemical class 0.000 description 1
- 238000006073 displacement reaction Methods 0.000 description 1
- 125000003438 dodecyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])* 0.000 description 1
- 210000002615 epidermis Anatomy 0.000 description 1
- CAMHHLOGFDZBBG-UHFFFAOYSA-N epoxidized methyl oleate Natural products CCCCCCCCC1OC1CCCCCCCC(=O)OC CAMHHLOGFDZBBG-UHFFFAOYSA-N 0.000 description 1
- 229940071106 ethylenediaminetetraacetate Drugs 0.000 description 1
- 238000011156 evaluation Methods 0.000 description 1
- 150000002190 fatty acyls Chemical group 0.000 description 1
- 239000011521 glass Substances 0.000 description 1
- 150000002306 glutamic acid derivatives Chemical class 0.000 description 1
- 238000005858 glycosidation reaction Methods 0.000 description 1
- 229930182470 glycoside Natural products 0.000 description 1
- 150000002338 glycosides Chemical group 0.000 description 1
- PCHJSUWPFVWCPO-UHFFFAOYSA-N gold Chemical compound [Au] PCHJSUWPFVWCPO-UHFFFAOYSA-N 0.000 description 1
- 239000010931 gold Substances 0.000 description 1
- 229910052737 gold Inorganic materials 0.000 description 1
- 238000007542 hardness measurement Methods 0.000 description 1
- 238000010438 heat treatment Methods 0.000 description 1
- SXCBDZAEHILGLM-UHFFFAOYSA-N heptane-1,7-diol Chemical compound OCCCCCCCO SXCBDZAEHILGLM-UHFFFAOYSA-N 0.000 description 1
- UBHWBODXJBSFLH-UHFFFAOYSA-N hexadecan-1-ol;octadecan-1-ol Chemical compound CCCCCCCCCCCCCCCCO.CCCCCCCCCCCCCCCCCCO UBHWBODXJBSFLH-UHFFFAOYSA-N 0.000 description 1
- QXDOUCFZSBCBMV-UHFFFAOYSA-N hexadecanoyloxymethanesulfonic acid Chemical compound S(=O)(=O)(O)COC(CCCCCCCCCCCCCCC)=O QXDOUCFZSBCBMV-UHFFFAOYSA-N 0.000 description 1
- 229930195733 hydrocarbon Natural products 0.000 description 1
- 150000002430 hydrocarbons Chemical class 0.000 description 1
- 229910052739 hydrogen Inorganic materials 0.000 description 1
- 239000003752 hydrotrope Substances 0.000 description 1
- 125000002887 hydroxy group Chemical group [H]O* 0.000 description 1
- 238000011065 in-situ storage Methods 0.000 description 1
- 230000000622 irritating effect Effects 0.000 description 1
- 239000000832 lactitol Substances 0.000 description 1
- VQHSOMBJVWLPSR-JVCRWLNRSA-N lactitol Chemical compound OC[C@H](O)[C@@H](O)[C@@H]([C@H](O)CO)O[C@@H]1O[C@H](CO)[C@H](O)[C@H](O)[C@H]1O VQHSOMBJVWLPSR-JVCRWLNRSA-N 0.000 description 1
- 235000010448 lactitol Nutrition 0.000 description 1
- 229960003451 lactitol Drugs 0.000 description 1
- 239000008101 lactose Substances 0.000 description 1
- LAPRIVJANDLWOK-UHFFFAOYSA-N laureth-5 Chemical compound CCCCCCCCCCCCOCCOCCOCCOCCOCCO LAPRIVJANDLWOK-UHFFFAOYSA-N 0.000 description 1
- 239000007791 liquid phase Substances 0.000 description 1
- 229910003002 lithium salt Inorganic materials 0.000 description 1
- 159000000002 lithium salts Chemical class 0.000 description 1
- KJSPVJJOPONRTK-UHFFFAOYSA-M lithium;tetradecanoate Chemical compound [Li+].CCCCCCCCCCCCCC([O-])=O KJSPVJJOPONRTK-UHFFFAOYSA-M 0.000 description 1
- 239000000347 magnesium hydroxide Substances 0.000 description 1
- 229910001862 magnesium hydroxide Inorganic materials 0.000 description 1
- 230000014759 maintenance of location Effects 0.000 description 1
- 239000000845 maltitol Substances 0.000 description 1
- 235000010449 maltitol Nutrition 0.000 description 1
- VQHSOMBJVWLPSR-WUJBLJFYSA-N maltitol Chemical compound OC[C@H](O)[C@@H](O)[C@@H]([C@H](O)CO)O[C@H]1O[C@H](CO)[C@@H](O)[C@H](O)[C@H]1O VQHSOMBJVWLPSR-WUJBLJFYSA-N 0.000 description 1
- 229940035436 maltitol Drugs 0.000 description 1
- 239000011159 matrix material Substances 0.000 description 1
- 239000002480 mineral oil Substances 0.000 description 1
- 235000010446 mineral oil Nutrition 0.000 description 1
- 239000012184 mineral wax Substances 0.000 description 1
- 230000001333 moisturizer Effects 0.000 description 1
- LPUQAYUQRXPFSQ-DFWYDOINSA-M monosodium L-glutamate Chemical compound [Na+].[O-]C(=O)[C@@H](N)CCC(O)=O LPUQAYUQRXPFSQ-DFWYDOINSA-M 0.000 description 1
- ONHFWHCMZAJCFB-UHFFFAOYSA-N myristamine oxide Chemical compound CCCCCCCCCCCCCC[N+](C)(C)[O-] ONHFWHCMZAJCFB-UHFFFAOYSA-N 0.000 description 1
- NHLUVTZJQOJKCC-UHFFFAOYSA-N n,n-dimethylhexadecan-1-amine Chemical compound CCCCCCCCCCCCCCCCN(C)C NHLUVTZJQOJKCC-UHFFFAOYSA-N 0.000 description 1
- WQEPLUUGTLDZJY-UHFFFAOYSA-N n-Pentadecanoic acid Natural products CCCCCCCCCCCCCCC(O)=O WQEPLUUGTLDZJY-UHFFFAOYSA-N 0.000 description 1
- ZAZKJZBWRNNLDS-UHFFFAOYSA-N n-tetradecanoic acid methyl ester Natural products CCCCCCCCCCCCCC(=O)OC ZAZKJZBWRNNLDS-UHFFFAOYSA-N 0.000 description 1
- 238000006386 neutralization reaction Methods 0.000 description 1
- 230000003472 neutralizing effect Effects 0.000 description 1
- FBUKVWPVBMHYJY-UHFFFAOYSA-N noncarboxylic acid Natural products CCCCCCCCC(O)=O FBUKVWPVBMHYJY-UHFFFAOYSA-N 0.000 description 1
- OQCDKBAXFALNLD-UHFFFAOYSA-N octadecanoic acid Natural products CCCCCCCC(C)CCCCCCCCC(O)=O OQCDKBAXFALNLD-UHFFFAOYSA-N 0.000 description 1
- HPEUJPJOZXNMSJ-UHFFFAOYSA-N octadecanoic acid methyl ester Natural products CCCCCCCCCCCCCCCCCC(=O)OC HPEUJPJOZXNMSJ-UHFFFAOYSA-N 0.000 description 1
- CKQVRZJOMJRTOY-UHFFFAOYSA-N octadecanoic acid;propane-1,2,3-triol Chemical compound OCC(O)CO.CCCCCCCCCCCCCCCCCC(O)=O CKQVRZJOMJRTOY-UHFFFAOYSA-N 0.000 description 1
- 230000009965 odorless effect Effects 0.000 description 1
- 239000003960 organic solvent Substances 0.000 description 1
- 239000003973 paint Substances 0.000 description 1
- 229910052763 palladium Inorganic materials 0.000 description 1
- 239000002540 palm oil Substances 0.000 description 1
- 125000000913 palmityl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 description 1
- 239000003208 petroleum Substances 0.000 description 1
- 239000012169 petroleum derived wax Substances 0.000 description 1
- 235000019381 petroleum wax Nutrition 0.000 description 1
- 239000010452 phosphate Substances 0.000 description 1
- 229920000573 polyethylene Polymers 0.000 description 1
- 235000011118 potassium hydroxide Nutrition 0.000 description 1
- 238000002360 preparation method Methods 0.000 description 1
- 230000002265 prevention Effects 0.000 description 1
- 238000012545 processing Methods 0.000 description 1
- MUPFEKGTMRGPLJ-ZQSKZDJDSA-N raffinose 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[C@@H]2[C@@H]([C@@H](O)[C@@H](O)[C@@H](CO)O2)O)O1 MUPFEKGTMRGPLJ-ZQSKZDJDSA-N 0.000 description 1
- 239000002994 raw material Substances 0.000 description 1
- 229940071089 sarcosinate Drugs 0.000 description 1
- 238000004626 scanning electron microscopy Methods 0.000 description 1
- 239000002453 shampoo Substances 0.000 description 1
- 229910052709 silver Inorganic materials 0.000 description 1
- 239000004332 silver Substances 0.000 description 1
- 238000011120 smear test Methods 0.000 description 1
- 239000008149 soap solution Substances 0.000 description 1
- 239000001632 sodium acetate Substances 0.000 description 1
- 235000017281 sodium acetate Nutrition 0.000 description 1
- 239000000429 sodium aluminium silicate Substances 0.000 description 1
- 235000012217 sodium aluminium silicate Nutrition 0.000 description 1
- URGAHOPLAPQHLN-UHFFFAOYSA-N sodium aluminosilicate Chemical compound [Na+].[Al+3].[O-][Si]([O-])=O.[O-][Si]([O-])=O URGAHOPLAPQHLN-UHFFFAOYSA-N 0.000 description 1
- 229940080236 sodium cetyl sulfate Drugs 0.000 description 1
- 239000001509 sodium citrate Substances 0.000 description 1
- NLJMYIDDQXHKNR-UHFFFAOYSA-K sodium citrate Chemical compound O.O.[Na+].[Na+].[Na+].[O-]C(=O)CC(O)(CC([O-])=O)C([O-])=O NLJMYIDDQXHKNR-UHFFFAOYSA-K 0.000 description 1
- 235000011083 sodium citrates Nutrition 0.000 description 1
- 229940079781 sodium cocoyl glutamate Drugs 0.000 description 1
- 229940079776 sodium cocoyl isethionate Drugs 0.000 description 1
- BTURAGWYSMTVOW-UHFFFAOYSA-M sodium dodecanoate Chemical compound [Na+].CCCCCCCCCCCC([O-])=O BTURAGWYSMTVOW-UHFFFAOYSA-M 0.000 description 1
- 229940082004 sodium laurate Drugs 0.000 description 1
- 229940057950 sodium laureth sulfate Drugs 0.000 description 1
- 229940079862 sodium lauryl sarcosinate Drugs 0.000 description 1
- 235000019333 sodium laurylsulphate Nutrition 0.000 description 1
- JWZSXZWCWMCYPE-RSAXXLAASA-M sodium;(4s)-4-amino-5-dodecoxy-5-oxopentanoate Chemical compound [Na+].CCCCCCCCCCCCOC(=O)[C@@H](N)CCC([O-])=O JWZSXZWCWMCYPE-RSAXXLAASA-M 0.000 description 1
- LWBVAHQZGAKXPU-BOXHHOBZSA-M sodium;(4s)-4-amino-5-octadecoxy-5-oxopentanoate Chemical compound [Na+].CCCCCCCCCCCCCCCCCCOC(=O)[C@@H](N)CCC([O-])=O LWBVAHQZGAKXPU-BOXHHOBZSA-M 0.000 description 1
- PWZDAQKVUDZPRI-LMOVPXPDSA-M sodium;(4s)-4-amino-5-oxo-5-tetradecoxypentanoate Chemical compound [Na+].CCCCCCCCCCCCCCOC(=O)[C@@H](N)CCC([O-])=O PWZDAQKVUDZPRI-LMOVPXPDSA-M 0.000 description 1
- SXHLENDCVBIJFO-UHFFFAOYSA-M sodium;2-[2-(2-dodecoxyethoxy)ethoxy]ethyl sulfate Chemical compound [Na+].CCCCCCCCCCCCOCCOCCOCCOS([O-])(=O)=O SXHLENDCVBIJFO-UHFFFAOYSA-M 0.000 description 1
- ADWNFGORSPBALY-UHFFFAOYSA-M sodium;2-[dodecyl(methyl)amino]acetate Chemical compound [Na+].CCCCCCCCCCCCN(C)CC([O-])=O ADWNFGORSPBALY-UHFFFAOYSA-M 0.000 description 1
- XOGAMNIYLGRUAZ-UHFFFAOYSA-N sodium;2-sulfohexadecanoic acid Chemical compound [Na].CCCCCCCCCCCCCCC(C(O)=O)S(O)(=O)=O XOGAMNIYLGRUAZ-UHFFFAOYSA-N 0.000 description 1
- ZDLIBIAEBFTEGZ-UHFFFAOYSA-N sodium;2-sulfooctadecanoic acid Chemical compound [Na].CCCCCCCCCCCCCCCCC(C(O)=O)S(O)(=O)=O ZDLIBIAEBFTEGZ-UHFFFAOYSA-N 0.000 description 1
- MWZFQMUXPSUDJQ-KVVVOXFISA-M sodium;[(z)-octadec-9-enyl] sulfate Chemical compound [Na+].CCCCCCCC\C=C/CCCCCCCCOS([O-])(=O)=O MWZFQMUXPSUDJQ-KVVVOXFISA-M 0.000 description 1
- GGHPAKFFUZUEKL-UHFFFAOYSA-M sodium;hexadecyl sulfate Chemical compound [Na+].CCCCCCCCCCCCCCCCOS([O-])(=O)=O GGHPAKFFUZUEKL-UHFFFAOYSA-M 0.000 description 1
- 239000008247 solid mixture Substances 0.000 description 1
- 230000003381 solubilizing effect Effects 0.000 description 1
- UQZIYBXSHAGNOE-XNSRJBNMSA-N stachyose 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[C@@H]2[C@@H]([C@@H](O)[C@@H](O)[C@@H](CO[C@@H]3[C@@H]([C@@H](O)[C@@H](O)[C@@H](CO)O3)O)O2)O)O1 UQZIYBXSHAGNOE-XNSRJBNMSA-N 0.000 description 1
- 239000008117 stearic acid Substances 0.000 description 1
- 238000003860 storage Methods 0.000 description 1
- 125000001424 substituent group Chemical group 0.000 description 1
- 238000006467 substitution reaction Methods 0.000 description 1
- BDHFUVZGWQCTTF-UHFFFAOYSA-M sulfonate Chemical compound [O-]S(=O)=O BDHFUVZGWQCTTF-UHFFFAOYSA-M 0.000 description 1
- 150000003467 sulfuric acid derivatives Chemical class 0.000 description 1
- 230000009967 tasteless effect Effects 0.000 description 1
- 239000012085 test solution Substances 0.000 description 1
- HQHCYKULIHKCEB-UHFFFAOYSA-N tetradecanedioic acid Natural products OC(=O)CCCCCCCCCCCCC(O)=O HQHCYKULIHKCEB-UHFFFAOYSA-N 0.000 description 1
- TUNFSRHWOTWDNC-HKGQFRNVSA-N tetradecanoic acid Chemical compound CCCCCCCCCCCCC[14C](O)=O TUNFSRHWOTWDNC-HKGQFRNVSA-N 0.000 description 1
- UEUXEKPTXMALOB-UHFFFAOYSA-J tetrasodium;2-[2-[bis(carboxylatomethyl)amino]ethyl-(carboxylatomethyl)amino]acetate Chemical compound [Na+].[Na+].[Na+].[Na+].[O-]C(=O)CN(CC([O-])=O)CCN(CC([O-])=O)CC([O-])=O UEUXEKPTXMALOB-UHFFFAOYSA-J 0.000 description 1
- PUVAFTRIIUSGLK-UHFFFAOYSA-M trimethyl(oxiran-2-ylmethyl)azanium;chloride Chemical compound [Cl-].C[N+](C)(C)CC1CO1 PUVAFTRIIUSGLK-UHFFFAOYSA-M 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C11—ANIMAL OR VEGETABLE OILS, FATS, FATTY SUBSTANCES OR WAXES; FATTY ACIDS THEREFROM; DETERGENTS; CANDLES
- C11D—DETERGENT COMPOSITIONS; USE OF SINGLE SUBSTANCES AS DETERGENTS; SOAP OR SOAP-MAKING; RESIN SOAPS; RECOVERY OF GLYCEROL
- C11D10/00—Compositions of detergents, not provided for by one single preceding group
- C11D10/04—Compositions of detergents, not provided for by one single preceding group based on mixtures of surface-active non-soap compounds and soap
- C11D10/042—Compositions of detergents, not provided for by one single preceding group based on mixtures of surface-active non-soap compounds and soap based on anionic surface-active compounds and soap
-
- C—CHEMISTRY; METALLURGY
- C11—ANIMAL OR VEGETABLE OILS, FATS, FATTY SUBSTANCES OR WAXES; FATTY ACIDS THEREFROM; DETERGENTS; CANDLES
- C11D—DETERGENT COMPOSITIONS; USE OF SINGLE SUBSTANCES AS DETERGENTS; SOAP OR SOAP-MAKING; RESIN SOAPS; RECOVERY OF GLYCEROL
- C11D1/00—Detergent compositions based essentially on surface-active compounds; Use of these compounds as a detergent
- C11D1/02—Anionic compounds
- C11D1/04—Carboxylic acids or salts thereof
-
- C—CHEMISTRY; METALLURGY
- C11—ANIMAL OR VEGETABLE OILS, FATS, FATTY SUBSTANCES OR WAXES; FATTY ACIDS THEREFROM; DETERGENTS; CANDLES
- C11D—DETERGENT COMPOSITIONS; USE OF SINGLE SUBSTANCES AS DETERGENTS; SOAP OR SOAP-MAKING; RESIN SOAPS; RECOVERY OF GLYCEROL
- C11D1/00—Detergent compositions based essentially on surface-active compounds; Use of these compounds as a detergent
- C11D1/02—Anionic compounds
- C11D1/04—Carboxylic acids or salts thereof
- C11D1/08—Polycarboxylic acids containing no nitrogen or sulfur
-
- C—CHEMISTRY; METALLURGY
- C11—ANIMAL OR VEGETABLE OILS, FATS, FATTY SUBSTANCES OR WAXES; FATTY ACIDS THEREFROM; DETERGENTS; CANDLES
- C11D—DETERGENT COMPOSITIONS; USE OF SINGLE SUBSTANCES AS DETERGENTS; SOAP OR SOAP-MAKING; RESIN SOAPS; RECOVERY OF GLYCEROL
- C11D10/00—Compositions of detergents, not provided for by one single preceding group
- C11D10/04—Compositions of detergents, not provided for by one single preceding group based on mixtures of surface-active non-soap compounds and soap
-
- C—CHEMISTRY; METALLURGY
- C11—ANIMAL OR VEGETABLE OILS, FATS, FATTY SUBSTANCES OR WAXES; FATTY ACIDS THEREFROM; DETERGENTS; CANDLES
- C11D—DETERGENT COMPOSITIONS; USE OF SINGLE SUBSTANCES AS DETERGENTS; SOAP OR SOAP-MAKING; RESIN SOAPS; RECOVERY OF GLYCEROL
- C11D10/00—Compositions of detergents, not provided for by one single preceding group
- C11D10/04—Compositions of detergents, not provided for by one single preceding group based on mixtures of surface-active non-soap compounds and soap
- C11D10/045—Compositions of detergents, not provided for by one single preceding group based on mixtures of surface-active non-soap compounds and soap based on non-ionic surface-active compounds and soap
-
- C—CHEMISTRY; METALLURGY
- C11—ANIMAL OR VEGETABLE OILS, FATS, FATTY SUBSTANCES OR WAXES; FATTY ACIDS THEREFROM; DETERGENTS; CANDLES
- C11D—DETERGENT COMPOSITIONS; USE OF SINGLE SUBSTANCES AS DETERGENTS; SOAP OR SOAP-MAKING; RESIN SOAPS; RECOVERY OF GLYCEROL
- C11D17/00—Detergent materials or soaps characterised by their shape or physical properties
- C11D17/0047—Detergents in the form of bars or tablets
- C11D17/006—Detergents in the form of bars or tablets containing mainly surfactants, but no builders, e.g. syndet bar
-
- C—CHEMISTRY; METALLURGY
- C11—ANIMAL OR VEGETABLE OILS, FATS, FATTY SUBSTANCES OR WAXES; FATTY ACIDS THEREFROM; DETERGENTS; CANDLES
- C11D—DETERGENT COMPOSITIONS; USE OF SINGLE SUBSTANCES AS DETERGENTS; SOAP OR SOAP-MAKING; RESIN SOAPS; RECOVERY OF GLYCEROL
- C11D17/00—Detergent materials or soaps characterised by their shape or physical properties
- C11D17/0047—Detergents in the form of bars or tablets
- C11D17/0065—Solid detergents containing builders
- C11D17/0069—Laundry bars
-
- C—CHEMISTRY; METALLURGY
- C11—ANIMAL OR VEGETABLE OILS, FATS, FATTY SUBSTANCES OR WAXES; FATTY ACIDS THEREFROM; DETERGENTS; CANDLES
- C11D—DETERGENT COMPOSITIONS; USE OF SINGLE SUBSTANCES AS DETERGENTS; SOAP OR SOAP-MAKING; RESIN SOAPS; RECOVERY OF GLYCEROL
- C11D1/00—Detergent compositions based essentially on surface-active compounds; Use of these compounds as a detergent
- C11D1/02—Anionic compounds
- C11D1/04—Carboxylic acids or salts thereof
- C11D1/10—Amino carboxylic acids; Imino carboxylic acids; Fatty acid condensates thereof
-
- C—CHEMISTRY; METALLURGY
- C11—ANIMAL OR VEGETABLE OILS, FATS, FATTY SUBSTANCES OR WAXES; FATTY ACIDS THEREFROM; DETERGENTS; CANDLES
- C11D—DETERGENT COMPOSITIONS; USE OF SINGLE SUBSTANCES AS DETERGENTS; SOAP OR SOAP-MAKING; RESIN SOAPS; RECOVERY OF GLYCEROL
- C11D1/00—Detergent compositions based essentially on surface-active compounds; Use of these compounds as a detergent
- C11D1/02—Anionic compounds
- C11D1/12—Sulfonic acids or sulfuric acid esters; Salts thereof
- C11D1/123—Sulfonic acids or sulfuric acid esters; Salts thereof derived from carboxylic acids, e.g. sulfosuccinates
-
- C—CHEMISTRY; METALLURGY
- C11—ANIMAL OR VEGETABLE OILS, FATS, FATTY SUBSTANCES OR WAXES; FATTY ACIDS THEREFROM; DETERGENTS; CANDLES
- C11D—DETERGENT COMPOSITIONS; USE OF SINGLE SUBSTANCES AS DETERGENTS; SOAP OR SOAP-MAKING; RESIN SOAPS; RECOVERY OF GLYCEROL
- C11D1/00—Detergent compositions based essentially on surface-active compounds; Use of these compounds as a detergent
- C11D1/02—Anionic compounds
- C11D1/12—Sulfonic acids or sulfuric acid esters; Salts thereof
- C11D1/126—Acylisethionates
-
- C—CHEMISTRY; METALLURGY
- C11—ANIMAL OR VEGETABLE OILS, FATS, FATTY SUBSTANCES OR WAXES; FATTY ACIDS THEREFROM; DETERGENTS; CANDLES
- C11D—DETERGENT COMPOSITIONS; USE OF SINGLE SUBSTANCES AS DETERGENTS; SOAP OR SOAP-MAKING; RESIN SOAPS; RECOVERY OF GLYCEROL
- C11D1/00—Detergent compositions based essentially on surface-active compounds; Use of these compounds as a detergent
- C11D1/02—Anionic compounds
- C11D1/12—Sulfonic acids or sulfuric acid esters; Salts thereof
- C11D1/14—Sulfonic acids or sulfuric acid esters; Salts thereof derived from aliphatic hydrocarbons or mono-alcohols
-
- C—CHEMISTRY; METALLURGY
- C11—ANIMAL OR VEGETABLE OILS, FATS, FATTY SUBSTANCES OR WAXES; FATTY ACIDS THEREFROM; DETERGENTS; CANDLES
- C11D—DETERGENT COMPOSITIONS; USE OF SINGLE SUBSTANCES AS DETERGENTS; SOAP OR SOAP-MAKING; RESIN SOAPS; RECOVERY OF GLYCEROL
- C11D1/00—Detergent compositions based essentially on surface-active compounds; Use of these compounds as a detergent
- C11D1/02—Anionic compounds
- C11D1/12—Sulfonic acids or sulfuric acid esters; Salts thereof
- C11D1/16—Sulfonic acids or sulfuric acid esters; Salts thereof derived from divalent or polyvalent alcohols
-
- C—CHEMISTRY; METALLURGY
- C11—ANIMAL OR VEGETABLE OILS, FATS, FATTY SUBSTANCES OR WAXES; FATTY ACIDS THEREFROM; DETERGENTS; CANDLES
- C11D—DETERGENT COMPOSITIONS; USE OF SINGLE SUBSTANCES AS DETERGENTS; SOAP OR SOAP-MAKING; RESIN SOAPS; RECOVERY OF GLYCEROL
- C11D1/00—Detergent compositions based essentially on surface-active compounds; Use of these compounds as a detergent
- C11D1/02—Anionic compounds
- C11D1/12—Sulfonic acids or sulfuric acid esters; Salts thereof
- C11D1/22—Sulfonic acids or sulfuric acid esters; Salts thereof derived from aromatic compounds
-
- C—CHEMISTRY; METALLURGY
- C11—ANIMAL OR VEGETABLE OILS, FATS, FATTY SUBSTANCES OR WAXES; FATTY ACIDS THEREFROM; DETERGENTS; CANDLES
- C11D—DETERGENT COMPOSITIONS; USE OF SINGLE SUBSTANCES AS DETERGENTS; SOAP OR SOAP-MAKING; RESIN SOAPS; RECOVERY OF GLYCEROL
- C11D1/00—Detergent compositions based essentially on surface-active compounds; Use of these compounds as a detergent
- C11D1/02—Anionic compounds
- C11D1/12—Sulfonic acids or sulfuric acid esters; Salts thereof
- C11D1/28—Sulfonation products derived from fatty acids or their derivatives, e.g. esters, amides
-
- C—CHEMISTRY; METALLURGY
- C11—ANIMAL OR VEGETABLE OILS, FATS, FATTY SUBSTANCES OR WAXES; FATTY ACIDS THEREFROM; DETERGENTS; CANDLES
- C11D—DETERGENT COMPOSITIONS; USE OF SINGLE SUBSTANCES AS DETERGENTS; SOAP OR SOAP-MAKING; RESIN SOAPS; RECOVERY OF GLYCEROL
- C11D1/00—Detergent compositions based essentially on surface-active compounds; Use of these compounds as a detergent
- C11D1/02—Anionic compounds
- C11D1/12—Sulfonic acids or sulfuric acid esters; Salts thereof
- C11D1/29—Sulfates of polyoxyalkylene ethers
-
- C—CHEMISTRY; METALLURGY
- C11—ANIMAL OR VEGETABLE OILS, FATS, FATTY SUBSTANCES OR WAXES; FATTY ACIDS THEREFROM; DETERGENTS; CANDLES
- C11D—DETERGENT COMPOSITIONS; USE OF SINGLE SUBSTANCES AS DETERGENTS; SOAP OR SOAP-MAKING; RESIN SOAPS; RECOVERY OF GLYCEROL
- C11D1/00—Detergent compositions based essentially on surface-active compounds; Use of these compounds as a detergent
- C11D1/02—Anionic compounds
- C11D1/32—Protein hydrolysates; Fatty acid condensates thereof
-
- C—CHEMISTRY; METALLURGY
- C11—ANIMAL OR VEGETABLE OILS, FATS, FATTY SUBSTANCES OR WAXES; FATTY ACIDS THEREFROM; DETERGENTS; CANDLES
- C11D—DETERGENT COMPOSITIONS; USE OF SINGLE SUBSTANCES AS DETERGENTS; SOAP OR SOAP-MAKING; RESIN SOAPS; RECOVERY OF GLYCEROL
- C11D1/00—Detergent compositions based essentially on surface-active compounds; Use of these compounds as a detergent
- C11D1/02—Anionic compounds
- C11D1/34—Derivatives of acids of phosphorus
- C11D1/345—Phosphates or phosphites
-
- C—CHEMISTRY; METALLURGY
- C11—ANIMAL OR VEGETABLE OILS, FATS, FATTY SUBSTANCES OR WAXES; FATTY ACIDS THEREFROM; DETERGENTS; CANDLES
- C11D—DETERGENT COMPOSITIONS; USE OF SINGLE SUBSTANCES AS DETERGENTS; SOAP OR SOAP-MAKING; RESIN SOAPS; RECOVERY OF GLYCEROL
- C11D1/00—Detergent compositions based essentially on surface-active compounds; Use of these compounds as a detergent
- C11D1/66—Non-ionic compounds
- C11D1/662—Carbohydrates or derivatives
-
- C—CHEMISTRY; METALLURGY
- C11—ANIMAL OR VEGETABLE OILS, FATS, FATTY SUBSTANCES OR WAXES; FATTY ACIDS THEREFROM; DETERGENTS; CANDLES
- C11D—DETERGENT COMPOSITIONS; USE OF SINGLE SUBSTANCES AS DETERGENTS; SOAP OR SOAP-MAKING; RESIN SOAPS; RECOVERY OF GLYCEROL
- C11D1/00—Detergent compositions based essentially on surface-active compounds; Use of these compounds as a detergent
- C11D1/66—Non-ionic compounds
- C11D1/75—Amino oxides
-
- C—CHEMISTRY; METALLURGY
- C11—ANIMAL OR VEGETABLE OILS, FATS, FATTY SUBSTANCES OR WAXES; FATTY ACIDS THEREFROM; DETERGENTS; CANDLES
- C11D—DETERGENT COMPOSITIONS; USE OF SINGLE SUBSTANCES AS DETERGENTS; SOAP OR SOAP-MAKING; RESIN SOAPS; RECOVERY OF GLYCEROL
- C11D1/00—Detergent compositions based essentially on surface-active compounds; Use of these compounds as a detergent
- C11D1/88—Ampholytes; Electroneutral compounds
- C11D1/90—Betaines
-
- C—CHEMISTRY; METALLURGY
- C11—ANIMAL OR VEGETABLE OILS, FATS, FATTY SUBSTANCES OR WAXES; FATTY ACIDS THEREFROM; DETERGENTS; CANDLES
- C11D—DETERGENT COMPOSITIONS; USE OF SINGLE SUBSTANCES AS DETERGENTS; SOAP OR SOAP-MAKING; RESIN SOAPS; RECOVERY OF GLYCEROL
- C11D1/00—Detergent compositions based essentially on surface-active compounds; Use of these compounds as a detergent
- C11D1/88—Ampholytes; Electroneutral compounds
- C11D1/92—Sulfobetaines ; Sulfitobetaines
Landscapes
- Chemical & Material Sciences (AREA)
- Life Sciences & Earth Sciences (AREA)
- Engineering & Computer Science (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Oil, Petroleum & Natural Gas (AREA)
- Wood Science & Technology (AREA)
- Organic Chemistry (AREA)
- Detergent Compositions (AREA)
- Cosmetics (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
- Catalysts (AREA)
- Materials For Medical Uses (AREA)
Abstract
The invention provides a shaped solid, three-dimensional skeleton structure comp rising: a relatively rigid, interlocking mesh of neutralized crystalline carboxylic acid. In another respect, the present invention provides an improved cleansing bar which is comprised of the rigid, interlocking mesh of neutralized carboxylic aci d, preferably sodium soap fibers. Such preferred cleansing bars can be formulated to have essentially no bar smear. Some cleansin g bars comprise surprisingly large amounts of water and another liquids while maintaining their rigidity and excellent smear p roperties; even when allowed to soak overnight in water.
Description
SHAPED SOLID MADE WITH A RIGID
INTERLOCKING MESH OF NEUTRALIZED CARBOXYLIC ACID
TECHNICAL FIELD
This invention relates to neutralized carboxylic acid shaped solid compositions, particularly cleansing bars, cakes, soap bars, synbars and the like.
Products made in the form of shaped solids, cakes and bars are numerous. Cleansing bars are well known in the art.
Cleansing bars with reduced bar smear are reported in the art. E.g., U.S. Pat. No. 2,988,511, Mills, issued June 13, 1961, discloses a low smearing bar.
Bar smear, also referred to as bar sloth, is the soft solid or mush that forms at the surface of a bar when submerged in water and is regarded by consumers as messy, unattractive, and uneconomical. Products made in the form of shaped solids, cakes and bars are numerous. E.g., certain high moisture and low smear personal cleansing bars are disclosed in U.S. Pat. No. 4,606,839 Harding, issued Aug. 19, 1986.
Harding uses coconut and/or palm kernel oil soap.
One only has to examine a used personal cleansing bars in their bathroom to see that there is still a need for improved cleansing bars with little or no smear.
The formation of rigid, soap curd fibers of sodium laurate is reported by L. Marton et al. in a 1940 Journal of American Chemical Society (Vol. 63, pp. 1990-1993). The report does not teach a B
INTERLOCKING MESH OF NEUTRALIZED CARBOXYLIC ACID
TECHNICAL FIELD
This invention relates to neutralized carboxylic acid shaped solid compositions, particularly cleansing bars, cakes, soap bars, synbars and the like.
Products made in the form of shaped solids, cakes and bars are numerous. Cleansing bars are well known in the art.
Cleansing bars with reduced bar smear are reported in the art. E.g., U.S. Pat. No. 2,988,511, Mills, issued June 13, 1961, discloses a low smearing bar.
Bar smear, also referred to as bar sloth, is the soft solid or mush that forms at the surface of a bar when submerged in water and is regarded by consumers as messy, unattractive, and uneconomical. Products made in the form of shaped solids, cakes and bars are numerous. E.g., certain high moisture and low smear personal cleansing bars are disclosed in U.S. Pat. No. 4,606,839 Harding, issued Aug. 19, 1986.
Harding uses coconut and/or palm kernel oil soap.
One only has to examine a used personal cleansing bars in their bathroom to see that there is still a need for improved cleansing bars with little or no smear.
The formation of rigid, soap curd fibers of sodium laurate is reported by L. Marton et al. in a 1940 Journal of American Chemical Society (Vol. 63, pp. 1990-1993). The report does not teach a B
- 2 ~ 3 ~ ~
utility for the soap curd. Shaped solids, as defined herein, are not disclosed by Marton et al.
Japanese Pat. J5 7030-798, July 30, 1980, discloses transparent solid framed or molded soap bar in which fatty acids constituting the soap component are myristic, palmitic, and stearic acids. A transparent soap is described in which at least 90 wt.% of the fatty acids which constitute the soap component are myristic acid, palmitic acid, and stearic acid. The product is reported as a transparent, solid soap having good frothing and solidifying properties, good storage stability, and a low irritant effect on human skin.
The process and transparent bar soap composition exemplified in Jap. J5 7030-798 do not appear to contain synthetic surfactant.
It is also difficult to produce firm, non-sticky bars that contain relatively high levels (15-40%) of moisture (especially in the presence of most synthetic surfactants), hygroscopic surfactants and/or higher levels of non-solids and soft solids, such as water-soluble polyols and hydrocarbon greases.
SUMMARY OF THE INVENTION
In accordance with one aspect of the invention there is provided A
personal cleansing bar composition comprising a rigid, crystalline interlocking mesh of elongated sodium soap crystals; said soap bar comprising:
from about 15% to about 50% sodium fatty acid soap composed of at least about 50% saturated fatty alkyl chains having 12-24 carbon atoms of which at least about 25% of said saturated fatty alkyl chains is of a single chain length;
from about 15% to about 60% water; and from about 2% to about 60% by weight of a hygroscopic synthetic surfactant wherein said hygroscopic synthetic surfactant is selected from surfactants which absorb at least about 20% of their dry weight in water at 26~C and 80% Relative Humidity in three days.
BRIEF DESCRIPTION OF THE FIGURES
Figures 1-8 show magnified views of bar samples of the present invention. Figures 9 and 10 show magnified views of two different conventional soap bars.
DETAILED DESCRIPTION OF FIGURES
The Scanning Electron Microscope (SEM) sample preparation involves fracturing a shaped solid with simple pressure to obtain a fresh surface for examination. The fractured sample is reduced B
W O 92/09679 3 2 0 9 5 3 51 P~/US91/08733 in size (razor blade) to approximately a 10 mm x 15 mm rectangle with a thickness of about 5 mm. The sample is mounted on an aluminum SEM stub using silver paint adhesive. The mounted sample is coated with approximately 300 angstroms of gold/palladium in a Pelco sputter coater. Prior to coating, the sample is subjected to vacuum for a period of time which is sufficient to allow sufficient loss of bar moisture assuring acceptable coating quality. After coating, the sample is transferred to the SEM
chamber and examined under standard SEM operating conditions with an Hitachi Model S570 Scanning Electron Microscope in order to see the skeletal (core) frame.
FIGS. 1 and 2 are copies of photographs of a highly enlarged skeleton core structure comprising a rigid, interlocking mesh of elongated neutralized carboxylic acid crystalline fibers. More specifically FIGS. 1 and 2 are elongated C12 sodium soap fibers, enlarged respectively at 5000X and 2500X magnifications. The structure of FIGS. 1 and 2 are made with 5% soap; 94% water; and 1% sodium chloride. See Example 10 in Table 7 herein. Note that larger fibers in the interlocking mesh can be composed of smaller fibers. Also, note the "void" spaces. See FIG. 2.
FIGS. 3, 4 and 5 are copies of photographs of a skeleton structure made with 25% sodium C12 soap; 74% water; and 1% sodium chloride. The crystalline fiber-like structure is shown respec-tively at 3000X, 5000X and 1000X magnifications.
FIG. 6 is a copy of a photograph of a skeleton structure made with 20% disodium salt of 1,12-dodecanedioic acid. The crystal-line fiber-like structure is shown at 2000X magnification. See Example 26.
FIG. 7 is a copy of a photograph of a skeleton (core) struc-ture comprising crystalline lithium neutralized C14 carboxylic acid mesh, shown at 1500X magnification. See Example 27.
FIG. 8 is a copy of a photograph of a cleansing bar (Exam-ple I hereinbelow) comprising: coated C14 16 sodium soap fibers.
The fibers are coated and/or commingled with the other bar compo-nents. The magnification is 1500X.
FIG. 9 shows a sample of a market IVORY~ freezer bar made with sodium/potassium coconut/tallow soap at 1000X on the scale.
CA 0209~3~1 1997-12-03 WO 92/09679 PCr/US91/08733 The air in the IVORY bar soap makes it float.
FIG. 10 shows a sample of a market NEUTROGENA~ transparent bar at 1500X.
In FIGS. 1 and 2, the samples are first melted on a hot plate and recooled on a glass slide. The other samples, FIGS. 3-10, are samples of original shaped solid structures or the conventional bar prepared as set out herein.
DETAILED DESCRIPTION OF THE INVENTION
The invention provides a shaped solid comprising two or more phases. One phase is a crystalline skeleton structure comprising a rigid interlocking, open, three-dimensional mesh of neutralized carboxylic acid elongated crystals. The other essential phase is an aqueous phase which is soft or flowable at 25-C.
More specifically, the skeleton structure is a relatively rigid, interlocking, open, three-dimensional mesh of neutralized mono- and/or di-carboxylic acid elongated crystals.
The terms: skeleton structure, skeletal structure, core, and skeleton frame are often used interchangeably herein.
The term "shaped solid" as used herein includes forms such as bars, cakes and the like. The term "bar" as used herein includes the same unless otherwise specified.
The term "mesh" as used herein means an interlocking crystal-line skeleton network with voids or openings when viewed under magnification by scanning electron microscopy.
In another respect, the present invention provides an improved cleansing bar which is comprised of said skeleton struc-ture. Some shaped solids are in the form of cleansing bars which contain surprisingly high levels of said aqueous phase comprising water, other liquids and soft materials. Notwithstanding the presence of relatively large levels of an aqueous phase. the preferred bars of the present invention maintain their rigidity and excellent smear properties, even when allowed to soak over-night in water. While not being bound to any theory, the shapea solid comprising these phases is similar to a relatively rigid we~
sponge.
The crystalline phase comprises crystals in the form of either interlocking platelets and~or fibers, preferably fibers.
CA 0209~3~1 1997-12-03 Preferably said fibers are composed of sodium soap. The inter-locking mesh of said fibers and/or platelets imparts strength to the three-dimensional structure, even in the presence of rela-tively high levels of water or other soft materials; even when allowed to soak overnight in water.
The strength of the skeleton structure can be measured indirectly by the hardness of the shaped solid, as determined by the resistance to penetration of the solid using a Standard Weighted Penetrometer Probe. See Bar Harness Test below for more details. The skeleton structure is of sufficient rigidity that a 20 mm thick or greater cleansing bar sample has a penetration of from about zero mm to about 12 mm, preferably from about l mm to about 10 mm, more preferably from about 3 mm to about 8 mm.
The present bars are distinguished from conventional trans-parent bars based on crystal size, as well as other character-istics. The crystals or crystal bundles that make-up the inter-locking mesh structure of the present invention preferably are of a size that diffracts light and consequently are greater than 400 nm in either diameter or length. On the other hand, conventional transparent bars gain their transparency by having crystal diameters or length less than the wavelength of white light, which is greater than about 400 nm and consequently do not diffract light.
Once formed, a bar (shaped solid) comprising the rigid skeletal structure of the present invention loses its rigidity when subjected to fracturing mechanical forces, e.g., those used in a conventional plodded bar making process as disclosed in U.S.
Pat. No. 4,812,253, Small et al., or U.S. Pat. No. 4,820,447, Medcalf et al. This is because the fracturing mechanical forces shear and break up the rigid, skeletal structure into smaller pieces. Thus, when a bar of the present invention is sheared in a plodder, a much softer bar results.
On the other hand, when a finished conventional bar is plodded or replodded, the replodded conventional bar is still very hard. See Example 28 and Table 12 for more details on this point.
W O 92/09679 2 0 9 5 3 S 1 - 6 - P~/US91/08733 The skeletal structure contains substantial "void" areas which are filled by soft and/or liquid aqueous phases. It is a surprising aspect of this invention that the physical properties of the bar, such as bar hardness and little smear, are mostly dependent on the crystalline interlocking mesh structure, even when the other phases make up a majority of the materials present.
In conventional bars, many components can impact the overall bar physical properties because the components either modify the phase and structure of the soap or synthetic surfactant components that primarily determine the bar's physical properties. The combina-tion of two or more phases (e.g., soap and aqueous solution) drastically changes the colloidal structure, and consequently, the physical properties of a conventional bar.
Thus, conventional bars are more limited in the type, levels and composition of soft phase materials that can be incorporated into the bar than the present invention. Such phases include most materials that are either flowable liquids or materials that are softer than the minimum hardness of an acceptable bar. These phases include aqueous solutions, liquid crystalline phases composed of water and surfactant, polymers; particularly sur-factant-containing crystalline phases, and especially hygroscopic surfactants, which tend to become soft and sticky when mixed with water or other liquid phases including water-soluble organics (e.g., propylene glycol and glycerine), hydrophobic materials (e.g., mineral oil, liquid triglycerides), or soft hydrophobic materials, e.g., petrolatum, low melting paraffin, and low melting triglycerides.
In physical terms, all these phases can be characterized as being flowable liquids or so soft that a Standard Weighted Pene-trometer Probe, as defined herein, will penetrate all the waythrough a 12 mm thick sample. These phases can be selectively included in the structure of the present invention without loss of the interlocking mesh structure and certain desirable physical properties.
209~351 DESCRIPTION OF PREFERRED EMBODIMENTS
The invention is a shaped solid comprising a skeleton struc-ture that is a relatively rigid interlocking, open three-dimen-sional mesh of neutralized mono- and/or di-carboxylic acid elon-gated crystals.
The preferred embodiment is a cleansing bar comprising at least two phases: (1) an aqueous phase having a penetration value of about 12 mm for a 12 mm deep sample; said aqueous phase being soft or flowable; (2) a rigid crystalline phase comprising a rigid crystalline phase skeleton structure comprising an interlocking, open three-dimensional mesh of neutralized mono- and/or di-car-boxylic acid elongated crystals; wherein said cleansing bar comprising said rigid crystalline phase skeleton structure and said aqueous phase has a penetration value of of from zero to about 12 mm for a 25 mm deep sample; and wherein said penetration values are measured as 25-C using a 247 gram Standard Weighted Penetrometer Probe having a conical needle attach to a 9 inch (22.9 cm) shaft weighing 47 grams, with 200 grams on top of said shaft for a total of said 247 grams, said conical needle having a 19/32 inch (1.51 cm) top and a 1/32 inch (0.08 cm) point.
The above cleansing bar is preferred when said neutralized carboxylic acid is selected from the group consisting of: lithium and/or sodium neutralized: monocarboxylic acid (soap) and/or dicarboxylic acid; and mixtures thereof; wherein said monocar-boxylic acid has a fatty alkyl(ene) chain of from about 12 to about 24 carbon atoms; wherein said dicarboxylic acid has a fatty alkyl(ene) chain of from about 12 to about 18 carbon atoms; and wherein at least about 80% of said carboxylic acid has saturated alkyl(ene) chains; and wherein said rigid crystalline phase skeleton structure occupies from about above 3% to about 75% of said cleansing bar by volume; and wherein said neutralized car-boxylic acid comprises from about above 5% to about 75%; and wherein said cleansing bar contains from about 15% to about less than 94% water by weight of said cleansing bar.
The above cleansing bar is preferred when at least 80%.
preferably 90%, of the carboxylic acid has the following general formula:
20y~ ~51 W O 92/09679 PC~r/US91/08733 H - (CH2Ja - CH - (CH2)b - C~2 - M+
I
X
wherein:
a + b = 8 to 20 - each a, b = O to 20 o X = H, OR, O-C-R, R, or mixtures thereof R = C1-C3 alkyl, H, or mixtures thereof M = Na, Li, or mixtures thereof.
The above cleansing bar is more preferred when said a + b =
10-16; each of said a, b = 0-16; said X = H, OR; R = H; and M =
Na.
The above cleansing bar is highly preferred when said elon-gated crystals are composed of fiber-like sodium fatty acid soap of which at least about 25% of said saturated fatty alkyl chains is of a single chain length; and wherein said bar contains: from about 15% to about 75% of said sodium soap; wherein the ratio of said unneutralized (free) carboxylic acid to soap is from about 1:2 to about 0. In other words, the free fatty acid is no more than 50% by weight of the soap in the formulation.
The above cleansing bar is preferred when said bar contains said sodium soap and water; and from about 2% to about 60% of a synthetic surfactant selected from the group consisting of: alkyl sulfates, paraffin sulfonates, alkylglycerylether sulfonates, acyl sarcosinates, methylacyl taurates, linear alkyl benzene sulfo-nates, N-acyl glutamates, alkyl glucosides, alpha sulfo fatty acid esters, acyl isethionates, alkyl sulfosuccinates, alkyl ether carboxylates, alkyl phosphate esters, ethoxylated alkyl phosphate esters, methyl glucose esters, protein condensates, alkyl amine oxides, alkyl betaines, alkyl sultaines, the alkyl ether sulfates with 1 to 12 ethoxy groups, and mixtures thereof, wherein said surfactants contain Cg-C22 alkyl chains.
The above cleansing bar is preferred when said synthetic sur-factant is hygroscopic; said hygroscopic surfactant being defined as a surfactant which absorbs at least 20% of its dry weight in 209~351 WO 92/09679 PCI'/US91/08733 g water at 26-C and 80% Relative Humidity in three days and wherein said bar is relatively non-swelling.
The above cleansing bar is preferred when said hygroscopic surfactant is selected from the group consisting of alpha sulfo 5 fatty acid esters; alkyl sulfates; alkyl ether carboxylates; alkyl betaines; alkyl sultaines; alkyl amine oxides; alkyl ether sul-fates; and mixtures thereof.
The above cleansing bar is preferred when the ratio of said water to said soap is from about 1:1 to about 5:1; said water is present at a level of from about 25% to about 60%; wherein said fatty alkyl chains are C14 to C22 and said soap level in said bar is from about 15% to about 35%; wherein at least about 85% of said alkyl chains are saturated; wherein the weight ratio of said unneutralized (free) carboxylic acid to said soap is from about 1:4 to 0; and wherein said synthetic surfactant level is from about 4% to about 25% by weight of the bar and said surfactant is selected from the group consisting of: sodium acyl isethionates, sodium acyl sarcosinates, sodium alpha sulfo fatty acid esters, sodium paraffin sulfonates, sodium alkyl ether sulfates, sodium alkyl sulfates, sodium linear alkyl benzene sulfonates, alkyl betaines, alkyl sultaines, and trialkyl amine oxides.
The above cleansing bar is preferred when the ratio of said water to soap ratio is from about 1.5:1 to about 2:1; the ratio of said unneutralized (free) carboxylic acid to said soap is from about 1:6 to 0; said water level is from about 30% to about 45%;
said fatty alkyl chain is from about C14 to about Clg; wherein at least about 95% of said alkyl chains are saturated; said soap level is from about 15% to about 30%; and said synthetic sur-factant level is from about 8% to about 16%.
The above cleansing bar is preferred when said bar contains from about 0.1% to about 40% of a hydrophobic material selected from the group consisting of: microcrystalline wax, petrolatum, carnauba wax, palm wax, candelilla wax, sugarcane wax, vegetable derived triglycerides, beeswax, spemaceti, lanolin, wood wax~
shellac wax, animal derived triglycerides, montar, ozokerite, ceresin, and Fischer-Tropsch wax.
20y53Sl - 10-The above cleansing bar is preferred when said bar contains from about 2% to about 35% of said hydrophobic material selected from the group consisting of petrolatum and wax, said petrolatum and wax, and mixtures thereof melting melting about 49-C (120-F) to about 85-C (185-F).
The above cleansing bar is preferred when said bar comprises from about 5% to about 25% by weight of the bar of paraffin wax.
The above cleansing bar is preferred when said bar contains from about 1% to about 50% of a non-volatile, water-soluble, nonionic organic material having a solubility of at least 5 parts in 10 parts of water; and wherein said water-soluble nonionic organic material is selected from the group consisting of a polyol of the structure:
Rl - O(CH2 - CHO)nH
where Rl = H, Cl-C4; R2 = H, CH3; and n = 1-200;
C2~C10 alkane diols; sorbitol; glycerine; sugars; sugar deriva-tives; urea; and ethanol amines of the general structure (HOCH2CH2)XNHy where x =
1-3; y = 0-2; and x+y = 3, and mixtures thereof.
The above cleansing bar is preferred when said bar contains from about 2% to about 40% of said non-volatile, water-soluble.
nonionic organic material.
The above cleansing bar is preferred when said non-volatile.
water-soluble, nonionic organic material comprises from about 5~~O
to about 20~o by weight of the bar; and wherein said organic material is selected from the group consisting of: propylene glycol, glycerine, sucrose, and urea, and mixtures thereof.
The above cleansing bar is preferred when said bar contains said sodium soap, said water, and said synthetic surfactant, and from about 0.1% to about 70% of other ingredients selected from the group consisting of:
from about 1% to about 10% said potassium soap;
from about 1% to about 35% said magnesium soap;
from about 1% to about 35% said calcium soap;
from about 1% to about 15% triethanolammonium soap;
WO 92/09679 2 0 9 5 3 5 1 PCI'/US91/08733 from about 1% to about 60% of impalpable water-insoluble materials selected from the group consisting of calcium carbonate and talc;
from about 0.1% to about 20% of a polymeric skin feel aid;
wherein said polymeric skin feel aid is selected from the group consisting of cationic polysaccharides, preferably cationic guar gum with molecular weights of 1,000 to 3,000,000; cationic polyalkylene imines, ethoxypolyalkylene imines, and poly[N-[-3-(dimethyl-ammonio)propyl]-N'-[3-ethyleneoxyethylene dimethylammo-nio)propyl]urea dichloride]; silicone gum; and silicone fluids; JR polymers; Celquat0;
from about 0.5% to about 25% of aluminosilicate clay and/or other clays; wherein said aluminosilicates and clays are selected from the group consisting of zeolites; kaolin, kaolinite, montmorillonite, attapulgite, illite, benton-ite, halloysite, and calcined clays;
from about 1% to about 50% of salt and salt hydrates; and mixtures thereof; and wherein said salt and salt hydrate have a cation selected from the group consisting of:
sodium, potassium, magnesium, calcium, aluminum, lithi-um, ammonium, monoethanol ammonium, diethanolammonium, and triethanolammonium; and wherein said salt and salt hydrate have an anion selected from the group consisting of: chloride, bromide, sulfate, metasilicate, ortho-phosphate, pyrophosphate, polyphosphate, metaborate tetraborate, carbonate, bicarbonate, hydrogen phosphate, methyl sulfate, and mono- and polycarboxylate of 6 carbon atoms or less.
The above cleansing bar is preferred when said elongated crystals contain platelets and wherein said soap consists of lithium neutralized monocarboxylic acid.
The above cleansing bar is preferred when said elongated crystals are fiber-like and wherein said neutralized dicarboxylic acid is the disodium salt 1,12-dodecanedioic acid and wherein said neutralized dicarboxylic acid comprises from about 20% to about 70% by weight of said bar.
2095351 ' ~ -W O 92/09679P ~ /US91/08733 A Preferred Process for Makinq the Bar A process of making the above preferred cleansing bar of the present invention comprises the steps of:
I. forming an aqueous molten liquid comprising about 15% to 5about 94% water and from about 6% to about 75% by weight said neutralized carboxylic acid;
II. pouring said molten liquid into a bar shaped mold; and III. crystallizing said molded molten liquid by cooling to provide said cleansing bar.
10The above process is preferred when the aqueous molten liquid is made by neutralizing an aqueous mixture of said carboxylic acid with sodium hydroxide or lithium hydroxide with stirring at a temperature of from about 50-C (120-F) to about 95-C (205-F).
The above process is preferred when from about 2% to about 1515% by weight of said bar is a "crystallization enhancing salt"
selected from the group consisting of: sodium or lithium salt of sulfate, chloride, acetate and citrate, and mixtures thereof.
The above process is preferred when said aqueous molten liquid aqueous phase contains from about 2% to about 40% of a 20solubilizing aid selected from the group consisting of:
(a) non-volatile, water-soluble nonionic organic solvents selected from the group consisting of: a polyol of the structure:
Rl - O(CH2 - CHO)nH
where Rl = H, C1-C4; R2 = H, CH3; and n = 1-200;
C2-C1o alkane diols; sorbitol; glycerine; sugars; sugar derivatives; urea; and ethanol amines of the general structure (HOCH2CH2)XNHy where x = 1-3; y = 0-2; and x+y = 3;
(b) alcohols of from 1 to 5 carbon atoms;
(c) synthetic surfactant selected from the group consisting of: alkyl sulfates, paraffin sulfonates, alkyl glyceryl ether sulfonates, anionic acyl sarcosinates, methyl acyl taurates, linear alkyl benzene sulfonates, N-acyl glutamates, alkyl glucosides, alpha sulfo fatty acid esters, acyl isethionates, alkyl sulfosuccinates, alkyl ether carboxylates, alkyl phosphate esters, ethoxylated alkyl phosphate esters, methyl glucose esters, protein condensates, alkyl amine oxides, alkyl betaines, alkyl sultaines, the alkyl ether sulfates with 1 to 12 ethoxy groups, and mixtures thereof, wherein said surfactants contain Cg-C22 alkylene chains; and mixtures thereof; and wherein said solubilizing aid is added to increase the level of said neutralized carboxylic acid dissolved in said con-tinuous molten aqueous phase in step I.
The above process is preferred when said aqueous phase contains from about 20~h to about 100% water by weight of said aqueous phase.
The above process is preferred when said rigid crystalline phase contains from about 75% to about 100% of said neutralized carboxylic acid by weight of said crystalline phase.
The above process is preferred when said bar has a pene-tration value of from about 3 mm to about 9 mm for said 25 mm bar sample.
The above process is preferred when said bar has miscel-laneous non-carboxylic acid phases comprising droplets or crystals selected from waxes, petrolatum, clays, and the like.
A highly preferred embodiment of the present invention is: a personal cleansing bar composition comprising a rigid, crystalline interlocking mesh of elongated sodium soap crystals; said soap bar comprising: from about 15% to about 50% sodium fatty acid soap composed of at least about 50% saturated fatty alkylene chains having 12-24 carbon atoms of which at least about 25% of said saturated fatty alkyl chains is of a single chain length; from about 15% to about 60% water; and from about 2% to about 60% by weight of a hygroscopic synthetic surfactant wherein said hygro-scopic synthetic surfactant is selected from surfactants which absorb at least about 20% of their dry weight in water at 26-C and 80% Relative Humidity in three days.
WO 92/09679 2 0 9 5 3 5 1 14 - PCl'/US91/0873J
The above highly preferred personal cleansing bar is more preferred when said hygroscopic synthetic surfactant is selected from the group consisting of alpha sulfo fatty acid esters; alkyl sulfates; alkyl ether carboxylates; alkyl betaines; alkyl sul-taines; alkyl amine oxides; alkyl ether sulfates; and mixturesthereof.
This highly preferred personal cleansing bar is more pre-ferred when said bar contains from about 0.5% to about 40% of salts and/or salt hydrates selected from the group consisting of:
sodium chloride, sodium sulfate, disodium hydrogen phosphate, sodium pyrophosphate, sodium tetraborate, sodium acetate, sodium citrate, and other compatible salts of inorganic acids and short chain organic acids.
A highly preferred cleansing bar comprises: various combi-nations of the core structure of sodium soap fibers, water, mildsynthetic surfactants, bar appearance stabilizers, skin mildness aides and other cleansing bar adjuvants. Such preferred bar can be formulated to have essentially no bar smear.
Some preferred bars of the present invention comprise: a rigid, interlocking mesh of neutralized carboxylic acid fiber-like core consisting essentially of sodium fatty acid soap composed of at least 50% saturated fatty alkyl chains having 12 to 24 carbon atoms. Preferably at least about 25% of said saturated alkyl chains are of a single chain length.
Some compositions of this invention comprise the above-defined rigid mesh with water and without water. These compo-sitions must be formed with water or another suitable solvent system. The compositions can be made with large amounts of water and the water level in the final composition can be reduced to as low as about 1% or 2%.
However, it is a special advantage of some structures de-scribed herein that they can be dehydrated without loss of the integrity of the mesh. Some preferred shaped solids can be dehydrated without appreciable change in their outer dimensions.
Other bars shrink while maintaining their three-dimensional form.
Some bars herein have the unique characteristic that they are not destroyed by dehydration.
W O 92/09679 P ~ /US91/08733 More complex bars of the present invention comprise a skele-tal structure comprising other salts of fatty acids selected from potassium, magnesiumt triethanolammonium and/or calcium soaps used in combination with the selected levels of sodium and/or lithium soaps. More complex cleansing bars can contain surprisingly large amounts of water, mild synthetic surfactants, bar appearance stabilizers, skin mildness aids and other cleansing bar adjuvants;
yet are mild and have very good low smear.
Tables 1-3 set out some preferred bars which are made with the sodium salts of the fatty carboxylic acid (FA) soap.
The percentages, ratios, and parts herein are on a total composition weight basis, unless otherwise specified. All levels and ranges herein are approximations unless otherwise specified.
TABLE l 15Preferred Bars~ Chain Lenqths and Levels More Most Preferred Preferred Preferred Water Level 15-94% 25-60% 30-45%
Water:Soap Ratio 0.7:1 1:1-5:1 1.5:1-2:1 FA Chain Length Cl2-24 Cl4-22 Cl4-l8 FA Soap Level in Total Formulation 6-50% 15-35% 15-30%
All highs and lows are not necessarily shown in Table 1. For example, some selected sodium soap can be used at a level up to about 75%. Thus, the range is from about 5% to about 75%. The preferred levels and ratios can vary from cation to cation, etc., and from mono- to polycarboxylic acids.
The bars shown in Table 1 are made with the level of water indicated, but the water level of the final bars can be reduced to provide bars which contain reduced levels of water or even little or no water. A preferred level of water is from about 20% to about 80% by weight of the bar.
Table 2 below shows some preferred levels of soaps of a single FA chain length. Table 3 shows some preferred levels of unsaturation in the FA's used in the compositions of the present WO 92/09679 2 o 9 5 3 5 1 - ! ~ PCI/US91/08733 invention. Some preferred compositions contain little or no short chain FA's of ten carbon atoms or less. The terms "soap", "fatty acid (FA) salts" and "monocarboxylic acid salts" as used herein are sometimes interchangeable. "Soap" is used since it is easier to relate to and is the preferred embodiment.
The % SoaD of Single Chain Lenqth (of Total Fibrous SoaD Content) More Most Preferred Preferred Preferred Cl2-24 25-100% 50-100% 75-100%
The Total % Unsaturated or Low (C1o or less) Chain Lenqth SoaDs More Broad Preferred Preferred Cl2 0-15% 0-5% 0-1%
C14-24 0-50% 0-10% 0-1%
The highs and lows of some key preferred optional ingredients for complex soap bar compositions of this invention are set out in Table 4. None of these ingredients is essential for the basic, preferred bar core structure. Zero is the lowest level for each optional ingredient. Some preferred bars can contain a total of from about 0.1% up to about 70% of such ingredients. The idea here is that the core bars can contain large amounts of other ingredients besides soap and water. The levels set out in Table 4 are particularly illustrative for bars containing from more than 5% to about 75% selected sodium soap and other ingredients.
It should be understood that solid shapes can be made with just lithium soap or just neutralized polycarboxylic acid, but would be expected to be somewhat different from the levels and ratios given for sodium soaps.
WO 92/096792 ~ 9 5 3 5 1 ~ ! ~ PCI'/US91 /08733 Hiqhs and Lows Wt.% of Other Inqredients for More ComDlex Sodium Soa~ Bars More Most 5Preferred Preferred Preferred Neutralized Dicar-boxylic Acid 1-40% 2-30% 5-25%
Lithium "Soap" 1-40% 2-30% 5-25%
Potassium Soap 1-10% 2-10% 5-8%
Magnesium or Calcium Soap 1-35% 1-12% 3-8%
Triethanolammonium Soap 1-15% 2-15% 5-10%
Synthetic Surfactant 1-60% 4-25% 8-16%
Other Salts and Salt Hydrates 0.5-50% 1-25% 2-15%
Non-Volatile, Water-Soluble Nonionic Organics 1.0-50% 2-40% 5-20%
Polymeric Mildness Enhancers 0.1-20% 0.25-10% 1-5%
Waxes 0.1-40% 2-35% 3-10%
Other Impalpable Water-insolubles 1-60% 4-25% 8-16%
Aluminosilicates/Clay 0.5-25% 1-10% 3-8%
The soaps useful in the present invention can be of the same alkyl chain lengths, i.e., which are selected from the 12 to 24 carbon atoms as set out in Table 2. The same chain lengths apply for the other non-sodium soaps used in the bars of the present invention.
The sodium soap is preferably at least about 50% of the soap present in the bar.
The levels of potassium soap and/or triethanolammonium soap should not exceed one-half, preferably one-third, more preferably less than one-fourth, that of the sodium soap and the level of -magnesium soap should not exceed about one-third of the level of sodium soap, and is preferably less than about one-fourth that of the sodium soap.
-- 18 ~ 3 ~ ~
The total of other soaps, save lithium soap, should preferably not exceed one-half, preferably one-third, of the sodium soap.
The synthetic detergent constituent of the bar compositions of the invention can be designated as being a detergent from the class consisting of anionic, nonionic, amphoteric and zwitterionic synthetic detergents. Both low and high lathering and high and low water-soluble surfactants can be used in the bar compositions of the present invention.
Examples of suitable synthetic detergents for use herein are those described in U.S. Pat. No. 3,351,558, Zimmerer, issued Nov. 7, 1967, at column 6, line 70 to column 7, line 74.
Examples include the water-soluble salts of organic, sulfonic a~k~
and of aliphatic sulfuric acid esters, that is, water-soluble salts of organic sulfuric reaction products having in the molecular structure an alkyl radical of from 10 to 22 carbon atoms and a radical selected from the group consisting of sulfonic acid and sulfuric acid ester radicals.
Synthetic sulfate detergents of special interest are the normally solid alkali metal salts of sulfuric acid esters of normal primary aliphatic alcohols having from 10 to 22 carbon atoms. Thus, the sodium and potassium salts of alkyl sulfuric acids obtained from the mixed higher alcohols derived by the reduction of tallow or by the reduction of coconut oil, palm oil, stearine, palm kernel oil, babassu kernel oil or other oils of the coconut group can be used herein.
Other aliphatic sulfuric acid esters which can be suitably employed include the water-soluble salts of sulfuric acid esters of polyhydric alcohols incompletely esterified with high molecular weight soap-forming carboxylic acids. Such synthetic detergents include the water-soluble alkali metal salts of sulfuric acid esters of higher molecular weight fatty acid monoglycerides such as the sodium and potassium salts of the coconut oil fatty acid monoester of 1,2-hydroxy-propane-3-sulfuric acid ester, sodium and potassium monomyristoyl ethylene glycol sulfate, and sodium and potassium monolauroyl diglycerol sulfate.
B
-The synthetic surfactants and other optional materials useful in conventional cleaning products are also useful in the present invention. In fact, some ingredients such as certain hygroscopic synthetic surfactants which are normally used in liquids and which are very difficult to incorporate into 5 normal cleansing bars are very compatible in the bars of the present invention. Thus, essentially all of the known synthetic surfactants which are useful in cleansing products are useful in the compositions of the present invention. The cleansing product patent literature is full of synthetic surfactant disclosures. Some preferred surfactants as well as other cleansing product ingredients are disclosed in the following references:
Pat. No. Issue Date Inventor(s) 4,061,602 12/1977 Oberstar et al.
4,234,464 11/1980 Morshauser 4,472,297 9/1984 Bolich et al.
4,491,539 1/1985 Hoskins et al.
4,540,507 9/1985 Grollier 4,565,647 1/1986 Ll enado 4,673,525 6/1987 Small et al.
4,704,224 11/1987 Saud 4,788,006 11/1988 Bolich, Jr., et al.
4,812,253 3/1989 Small et al.
4,820,447 4/1989 Medcalf et al.
4,906,459 3/1990 Cobb et al.
4,923,635 5/1990 Simion et al.
4,954,282 9/1990 Rys et al.
Some preferred synthetic surfactants are shown the Examples herein. Preferred synthetic surfactant systems are selectively designed for bar appearance stability, lather, cleansing and mildness.
It is noted that surfactant mildness can be measured by a skin barrier 30 destruction test which is used to assess the irritancy potential ofsurfactants. In this test the milder the surfactant, the lesser the skin barrier is destroyed. Skin barrier destruction is measured by the relative amount of radio-labeled water (3H-H2o) which passes from the test solution through the skin epidermis into the physiological buffer contained in the B
utility for the soap curd. Shaped solids, as defined herein, are not disclosed by Marton et al.
Japanese Pat. J5 7030-798, July 30, 1980, discloses transparent solid framed or molded soap bar in which fatty acids constituting the soap component are myristic, palmitic, and stearic acids. A transparent soap is described in which at least 90 wt.% of the fatty acids which constitute the soap component are myristic acid, palmitic acid, and stearic acid. The product is reported as a transparent, solid soap having good frothing and solidifying properties, good storage stability, and a low irritant effect on human skin.
The process and transparent bar soap composition exemplified in Jap. J5 7030-798 do not appear to contain synthetic surfactant.
It is also difficult to produce firm, non-sticky bars that contain relatively high levels (15-40%) of moisture (especially in the presence of most synthetic surfactants), hygroscopic surfactants and/or higher levels of non-solids and soft solids, such as water-soluble polyols and hydrocarbon greases.
SUMMARY OF THE INVENTION
In accordance with one aspect of the invention there is provided A
personal cleansing bar composition comprising a rigid, crystalline interlocking mesh of elongated sodium soap crystals; said soap bar comprising:
from about 15% to about 50% sodium fatty acid soap composed of at least about 50% saturated fatty alkyl chains having 12-24 carbon atoms of which at least about 25% of said saturated fatty alkyl chains is of a single chain length;
from about 15% to about 60% water; and from about 2% to about 60% by weight of a hygroscopic synthetic surfactant wherein said hygroscopic synthetic surfactant is selected from surfactants which absorb at least about 20% of their dry weight in water at 26~C and 80% Relative Humidity in three days.
BRIEF DESCRIPTION OF THE FIGURES
Figures 1-8 show magnified views of bar samples of the present invention. Figures 9 and 10 show magnified views of two different conventional soap bars.
DETAILED DESCRIPTION OF FIGURES
The Scanning Electron Microscope (SEM) sample preparation involves fracturing a shaped solid with simple pressure to obtain a fresh surface for examination. The fractured sample is reduced B
W O 92/09679 3 2 0 9 5 3 51 P~/US91/08733 in size (razor blade) to approximately a 10 mm x 15 mm rectangle with a thickness of about 5 mm. The sample is mounted on an aluminum SEM stub using silver paint adhesive. The mounted sample is coated with approximately 300 angstroms of gold/palladium in a Pelco sputter coater. Prior to coating, the sample is subjected to vacuum for a period of time which is sufficient to allow sufficient loss of bar moisture assuring acceptable coating quality. After coating, the sample is transferred to the SEM
chamber and examined under standard SEM operating conditions with an Hitachi Model S570 Scanning Electron Microscope in order to see the skeletal (core) frame.
FIGS. 1 and 2 are copies of photographs of a highly enlarged skeleton core structure comprising a rigid, interlocking mesh of elongated neutralized carboxylic acid crystalline fibers. More specifically FIGS. 1 and 2 are elongated C12 sodium soap fibers, enlarged respectively at 5000X and 2500X magnifications. The structure of FIGS. 1 and 2 are made with 5% soap; 94% water; and 1% sodium chloride. See Example 10 in Table 7 herein. Note that larger fibers in the interlocking mesh can be composed of smaller fibers. Also, note the "void" spaces. See FIG. 2.
FIGS. 3, 4 and 5 are copies of photographs of a skeleton structure made with 25% sodium C12 soap; 74% water; and 1% sodium chloride. The crystalline fiber-like structure is shown respec-tively at 3000X, 5000X and 1000X magnifications.
FIG. 6 is a copy of a photograph of a skeleton structure made with 20% disodium salt of 1,12-dodecanedioic acid. The crystal-line fiber-like structure is shown at 2000X magnification. See Example 26.
FIG. 7 is a copy of a photograph of a skeleton (core) struc-ture comprising crystalline lithium neutralized C14 carboxylic acid mesh, shown at 1500X magnification. See Example 27.
FIG. 8 is a copy of a photograph of a cleansing bar (Exam-ple I hereinbelow) comprising: coated C14 16 sodium soap fibers.
The fibers are coated and/or commingled with the other bar compo-nents. The magnification is 1500X.
FIG. 9 shows a sample of a market IVORY~ freezer bar made with sodium/potassium coconut/tallow soap at 1000X on the scale.
CA 0209~3~1 1997-12-03 WO 92/09679 PCr/US91/08733 The air in the IVORY bar soap makes it float.
FIG. 10 shows a sample of a market NEUTROGENA~ transparent bar at 1500X.
In FIGS. 1 and 2, the samples are first melted on a hot plate and recooled on a glass slide. The other samples, FIGS. 3-10, are samples of original shaped solid structures or the conventional bar prepared as set out herein.
DETAILED DESCRIPTION OF THE INVENTION
The invention provides a shaped solid comprising two or more phases. One phase is a crystalline skeleton structure comprising a rigid interlocking, open, three-dimensional mesh of neutralized carboxylic acid elongated crystals. The other essential phase is an aqueous phase which is soft or flowable at 25-C.
More specifically, the skeleton structure is a relatively rigid, interlocking, open, three-dimensional mesh of neutralized mono- and/or di-carboxylic acid elongated crystals.
The terms: skeleton structure, skeletal structure, core, and skeleton frame are often used interchangeably herein.
The term "shaped solid" as used herein includes forms such as bars, cakes and the like. The term "bar" as used herein includes the same unless otherwise specified.
The term "mesh" as used herein means an interlocking crystal-line skeleton network with voids or openings when viewed under magnification by scanning electron microscopy.
In another respect, the present invention provides an improved cleansing bar which is comprised of said skeleton struc-ture. Some shaped solids are in the form of cleansing bars which contain surprisingly high levels of said aqueous phase comprising water, other liquids and soft materials. Notwithstanding the presence of relatively large levels of an aqueous phase. the preferred bars of the present invention maintain their rigidity and excellent smear properties, even when allowed to soak over-night in water. While not being bound to any theory, the shapea solid comprising these phases is similar to a relatively rigid we~
sponge.
The crystalline phase comprises crystals in the form of either interlocking platelets and~or fibers, preferably fibers.
CA 0209~3~1 1997-12-03 Preferably said fibers are composed of sodium soap. The inter-locking mesh of said fibers and/or platelets imparts strength to the three-dimensional structure, even in the presence of rela-tively high levels of water or other soft materials; even when allowed to soak overnight in water.
The strength of the skeleton structure can be measured indirectly by the hardness of the shaped solid, as determined by the resistance to penetration of the solid using a Standard Weighted Penetrometer Probe. See Bar Harness Test below for more details. The skeleton structure is of sufficient rigidity that a 20 mm thick or greater cleansing bar sample has a penetration of from about zero mm to about 12 mm, preferably from about l mm to about 10 mm, more preferably from about 3 mm to about 8 mm.
The present bars are distinguished from conventional trans-parent bars based on crystal size, as well as other character-istics. The crystals or crystal bundles that make-up the inter-locking mesh structure of the present invention preferably are of a size that diffracts light and consequently are greater than 400 nm in either diameter or length. On the other hand, conventional transparent bars gain their transparency by having crystal diameters or length less than the wavelength of white light, which is greater than about 400 nm and consequently do not diffract light.
Once formed, a bar (shaped solid) comprising the rigid skeletal structure of the present invention loses its rigidity when subjected to fracturing mechanical forces, e.g., those used in a conventional plodded bar making process as disclosed in U.S.
Pat. No. 4,812,253, Small et al., or U.S. Pat. No. 4,820,447, Medcalf et al. This is because the fracturing mechanical forces shear and break up the rigid, skeletal structure into smaller pieces. Thus, when a bar of the present invention is sheared in a plodder, a much softer bar results.
On the other hand, when a finished conventional bar is plodded or replodded, the replodded conventional bar is still very hard. See Example 28 and Table 12 for more details on this point.
W O 92/09679 2 0 9 5 3 S 1 - 6 - P~/US91/08733 The skeletal structure contains substantial "void" areas which are filled by soft and/or liquid aqueous phases. It is a surprising aspect of this invention that the physical properties of the bar, such as bar hardness and little smear, are mostly dependent on the crystalline interlocking mesh structure, even when the other phases make up a majority of the materials present.
In conventional bars, many components can impact the overall bar physical properties because the components either modify the phase and structure of the soap or synthetic surfactant components that primarily determine the bar's physical properties. The combina-tion of two or more phases (e.g., soap and aqueous solution) drastically changes the colloidal structure, and consequently, the physical properties of a conventional bar.
Thus, conventional bars are more limited in the type, levels and composition of soft phase materials that can be incorporated into the bar than the present invention. Such phases include most materials that are either flowable liquids or materials that are softer than the minimum hardness of an acceptable bar. These phases include aqueous solutions, liquid crystalline phases composed of water and surfactant, polymers; particularly sur-factant-containing crystalline phases, and especially hygroscopic surfactants, which tend to become soft and sticky when mixed with water or other liquid phases including water-soluble organics (e.g., propylene glycol and glycerine), hydrophobic materials (e.g., mineral oil, liquid triglycerides), or soft hydrophobic materials, e.g., petrolatum, low melting paraffin, and low melting triglycerides.
In physical terms, all these phases can be characterized as being flowable liquids or so soft that a Standard Weighted Pene-trometer Probe, as defined herein, will penetrate all the waythrough a 12 mm thick sample. These phases can be selectively included in the structure of the present invention without loss of the interlocking mesh structure and certain desirable physical properties.
209~351 DESCRIPTION OF PREFERRED EMBODIMENTS
The invention is a shaped solid comprising a skeleton struc-ture that is a relatively rigid interlocking, open three-dimen-sional mesh of neutralized mono- and/or di-carboxylic acid elon-gated crystals.
The preferred embodiment is a cleansing bar comprising at least two phases: (1) an aqueous phase having a penetration value of about 12 mm for a 12 mm deep sample; said aqueous phase being soft or flowable; (2) a rigid crystalline phase comprising a rigid crystalline phase skeleton structure comprising an interlocking, open three-dimensional mesh of neutralized mono- and/or di-car-boxylic acid elongated crystals; wherein said cleansing bar comprising said rigid crystalline phase skeleton structure and said aqueous phase has a penetration value of of from zero to about 12 mm for a 25 mm deep sample; and wherein said penetration values are measured as 25-C using a 247 gram Standard Weighted Penetrometer Probe having a conical needle attach to a 9 inch (22.9 cm) shaft weighing 47 grams, with 200 grams on top of said shaft for a total of said 247 grams, said conical needle having a 19/32 inch (1.51 cm) top and a 1/32 inch (0.08 cm) point.
The above cleansing bar is preferred when said neutralized carboxylic acid is selected from the group consisting of: lithium and/or sodium neutralized: monocarboxylic acid (soap) and/or dicarboxylic acid; and mixtures thereof; wherein said monocar-boxylic acid has a fatty alkyl(ene) chain of from about 12 to about 24 carbon atoms; wherein said dicarboxylic acid has a fatty alkyl(ene) chain of from about 12 to about 18 carbon atoms; and wherein at least about 80% of said carboxylic acid has saturated alkyl(ene) chains; and wherein said rigid crystalline phase skeleton structure occupies from about above 3% to about 75% of said cleansing bar by volume; and wherein said neutralized car-boxylic acid comprises from about above 5% to about 75%; and wherein said cleansing bar contains from about 15% to about less than 94% water by weight of said cleansing bar.
The above cleansing bar is preferred when at least 80%.
preferably 90%, of the carboxylic acid has the following general formula:
20y~ ~51 W O 92/09679 PC~r/US91/08733 H - (CH2Ja - CH - (CH2)b - C~2 - M+
I
X
wherein:
a + b = 8 to 20 - each a, b = O to 20 o X = H, OR, O-C-R, R, or mixtures thereof R = C1-C3 alkyl, H, or mixtures thereof M = Na, Li, or mixtures thereof.
The above cleansing bar is more preferred when said a + b =
10-16; each of said a, b = 0-16; said X = H, OR; R = H; and M =
Na.
The above cleansing bar is highly preferred when said elon-gated crystals are composed of fiber-like sodium fatty acid soap of which at least about 25% of said saturated fatty alkyl chains is of a single chain length; and wherein said bar contains: from about 15% to about 75% of said sodium soap; wherein the ratio of said unneutralized (free) carboxylic acid to soap is from about 1:2 to about 0. In other words, the free fatty acid is no more than 50% by weight of the soap in the formulation.
The above cleansing bar is preferred when said bar contains said sodium soap and water; and from about 2% to about 60% of a synthetic surfactant selected from the group consisting of: alkyl sulfates, paraffin sulfonates, alkylglycerylether sulfonates, acyl sarcosinates, methylacyl taurates, linear alkyl benzene sulfo-nates, N-acyl glutamates, alkyl glucosides, alpha sulfo fatty acid esters, acyl isethionates, alkyl sulfosuccinates, alkyl ether carboxylates, alkyl phosphate esters, ethoxylated alkyl phosphate esters, methyl glucose esters, protein condensates, alkyl amine oxides, alkyl betaines, alkyl sultaines, the alkyl ether sulfates with 1 to 12 ethoxy groups, and mixtures thereof, wherein said surfactants contain Cg-C22 alkyl chains.
The above cleansing bar is preferred when said synthetic sur-factant is hygroscopic; said hygroscopic surfactant being defined as a surfactant which absorbs at least 20% of its dry weight in 209~351 WO 92/09679 PCI'/US91/08733 g water at 26-C and 80% Relative Humidity in three days and wherein said bar is relatively non-swelling.
The above cleansing bar is preferred when said hygroscopic surfactant is selected from the group consisting of alpha sulfo 5 fatty acid esters; alkyl sulfates; alkyl ether carboxylates; alkyl betaines; alkyl sultaines; alkyl amine oxides; alkyl ether sul-fates; and mixtures thereof.
The above cleansing bar is preferred when the ratio of said water to said soap is from about 1:1 to about 5:1; said water is present at a level of from about 25% to about 60%; wherein said fatty alkyl chains are C14 to C22 and said soap level in said bar is from about 15% to about 35%; wherein at least about 85% of said alkyl chains are saturated; wherein the weight ratio of said unneutralized (free) carboxylic acid to said soap is from about 1:4 to 0; and wherein said synthetic surfactant level is from about 4% to about 25% by weight of the bar and said surfactant is selected from the group consisting of: sodium acyl isethionates, sodium acyl sarcosinates, sodium alpha sulfo fatty acid esters, sodium paraffin sulfonates, sodium alkyl ether sulfates, sodium alkyl sulfates, sodium linear alkyl benzene sulfonates, alkyl betaines, alkyl sultaines, and trialkyl amine oxides.
The above cleansing bar is preferred when the ratio of said water to soap ratio is from about 1.5:1 to about 2:1; the ratio of said unneutralized (free) carboxylic acid to said soap is from about 1:6 to 0; said water level is from about 30% to about 45%;
said fatty alkyl chain is from about C14 to about Clg; wherein at least about 95% of said alkyl chains are saturated; said soap level is from about 15% to about 30%; and said synthetic sur-factant level is from about 8% to about 16%.
The above cleansing bar is preferred when said bar contains from about 0.1% to about 40% of a hydrophobic material selected from the group consisting of: microcrystalline wax, petrolatum, carnauba wax, palm wax, candelilla wax, sugarcane wax, vegetable derived triglycerides, beeswax, spemaceti, lanolin, wood wax~
shellac wax, animal derived triglycerides, montar, ozokerite, ceresin, and Fischer-Tropsch wax.
20y53Sl - 10-The above cleansing bar is preferred when said bar contains from about 2% to about 35% of said hydrophobic material selected from the group consisting of petrolatum and wax, said petrolatum and wax, and mixtures thereof melting melting about 49-C (120-F) to about 85-C (185-F).
The above cleansing bar is preferred when said bar comprises from about 5% to about 25% by weight of the bar of paraffin wax.
The above cleansing bar is preferred when said bar contains from about 1% to about 50% of a non-volatile, water-soluble, nonionic organic material having a solubility of at least 5 parts in 10 parts of water; and wherein said water-soluble nonionic organic material is selected from the group consisting of a polyol of the structure:
Rl - O(CH2 - CHO)nH
where Rl = H, Cl-C4; R2 = H, CH3; and n = 1-200;
C2~C10 alkane diols; sorbitol; glycerine; sugars; sugar deriva-tives; urea; and ethanol amines of the general structure (HOCH2CH2)XNHy where x =
1-3; y = 0-2; and x+y = 3, and mixtures thereof.
The above cleansing bar is preferred when said bar contains from about 2% to about 40% of said non-volatile, water-soluble.
nonionic organic material.
The above cleansing bar is preferred when said non-volatile.
water-soluble, nonionic organic material comprises from about 5~~O
to about 20~o by weight of the bar; and wherein said organic material is selected from the group consisting of: propylene glycol, glycerine, sucrose, and urea, and mixtures thereof.
The above cleansing bar is preferred when said bar contains said sodium soap, said water, and said synthetic surfactant, and from about 0.1% to about 70% of other ingredients selected from the group consisting of:
from about 1% to about 10% said potassium soap;
from about 1% to about 35% said magnesium soap;
from about 1% to about 35% said calcium soap;
from about 1% to about 15% triethanolammonium soap;
WO 92/09679 2 0 9 5 3 5 1 PCI'/US91/08733 from about 1% to about 60% of impalpable water-insoluble materials selected from the group consisting of calcium carbonate and talc;
from about 0.1% to about 20% of a polymeric skin feel aid;
wherein said polymeric skin feel aid is selected from the group consisting of cationic polysaccharides, preferably cationic guar gum with molecular weights of 1,000 to 3,000,000; cationic polyalkylene imines, ethoxypolyalkylene imines, and poly[N-[-3-(dimethyl-ammonio)propyl]-N'-[3-ethyleneoxyethylene dimethylammo-nio)propyl]urea dichloride]; silicone gum; and silicone fluids; JR polymers; Celquat0;
from about 0.5% to about 25% of aluminosilicate clay and/or other clays; wherein said aluminosilicates and clays are selected from the group consisting of zeolites; kaolin, kaolinite, montmorillonite, attapulgite, illite, benton-ite, halloysite, and calcined clays;
from about 1% to about 50% of salt and salt hydrates; and mixtures thereof; and wherein said salt and salt hydrate have a cation selected from the group consisting of:
sodium, potassium, magnesium, calcium, aluminum, lithi-um, ammonium, monoethanol ammonium, diethanolammonium, and triethanolammonium; and wherein said salt and salt hydrate have an anion selected from the group consisting of: chloride, bromide, sulfate, metasilicate, ortho-phosphate, pyrophosphate, polyphosphate, metaborate tetraborate, carbonate, bicarbonate, hydrogen phosphate, methyl sulfate, and mono- and polycarboxylate of 6 carbon atoms or less.
The above cleansing bar is preferred when said elongated crystals contain platelets and wherein said soap consists of lithium neutralized monocarboxylic acid.
The above cleansing bar is preferred when said elongated crystals are fiber-like and wherein said neutralized dicarboxylic acid is the disodium salt 1,12-dodecanedioic acid and wherein said neutralized dicarboxylic acid comprises from about 20% to about 70% by weight of said bar.
2095351 ' ~ -W O 92/09679P ~ /US91/08733 A Preferred Process for Makinq the Bar A process of making the above preferred cleansing bar of the present invention comprises the steps of:
I. forming an aqueous molten liquid comprising about 15% to 5about 94% water and from about 6% to about 75% by weight said neutralized carboxylic acid;
II. pouring said molten liquid into a bar shaped mold; and III. crystallizing said molded molten liquid by cooling to provide said cleansing bar.
10The above process is preferred when the aqueous molten liquid is made by neutralizing an aqueous mixture of said carboxylic acid with sodium hydroxide or lithium hydroxide with stirring at a temperature of from about 50-C (120-F) to about 95-C (205-F).
The above process is preferred when from about 2% to about 1515% by weight of said bar is a "crystallization enhancing salt"
selected from the group consisting of: sodium or lithium salt of sulfate, chloride, acetate and citrate, and mixtures thereof.
The above process is preferred when said aqueous molten liquid aqueous phase contains from about 2% to about 40% of a 20solubilizing aid selected from the group consisting of:
(a) non-volatile, water-soluble nonionic organic solvents selected from the group consisting of: a polyol of the structure:
Rl - O(CH2 - CHO)nH
where Rl = H, C1-C4; R2 = H, CH3; and n = 1-200;
C2-C1o alkane diols; sorbitol; glycerine; sugars; sugar derivatives; urea; and ethanol amines of the general structure (HOCH2CH2)XNHy where x = 1-3; y = 0-2; and x+y = 3;
(b) alcohols of from 1 to 5 carbon atoms;
(c) synthetic surfactant selected from the group consisting of: alkyl sulfates, paraffin sulfonates, alkyl glyceryl ether sulfonates, anionic acyl sarcosinates, methyl acyl taurates, linear alkyl benzene sulfonates, N-acyl glutamates, alkyl glucosides, alpha sulfo fatty acid esters, acyl isethionates, alkyl sulfosuccinates, alkyl ether carboxylates, alkyl phosphate esters, ethoxylated alkyl phosphate esters, methyl glucose esters, protein condensates, alkyl amine oxides, alkyl betaines, alkyl sultaines, the alkyl ether sulfates with 1 to 12 ethoxy groups, and mixtures thereof, wherein said surfactants contain Cg-C22 alkylene chains; and mixtures thereof; and wherein said solubilizing aid is added to increase the level of said neutralized carboxylic acid dissolved in said con-tinuous molten aqueous phase in step I.
The above process is preferred when said aqueous phase contains from about 20~h to about 100% water by weight of said aqueous phase.
The above process is preferred when said rigid crystalline phase contains from about 75% to about 100% of said neutralized carboxylic acid by weight of said crystalline phase.
The above process is preferred when said bar has a pene-tration value of from about 3 mm to about 9 mm for said 25 mm bar sample.
The above process is preferred when said bar has miscel-laneous non-carboxylic acid phases comprising droplets or crystals selected from waxes, petrolatum, clays, and the like.
A highly preferred embodiment of the present invention is: a personal cleansing bar composition comprising a rigid, crystalline interlocking mesh of elongated sodium soap crystals; said soap bar comprising: from about 15% to about 50% sodium fatty acid soap composed of at least about 50% saturated fatty alkylene chains having 12-24 carbon atoms of which at least about 25% of said saturated fatty alkyl chains is of a single chain length; from about 15% to about 60% water; and from about 2% to about 60% by weight of a hygroscopic synthetic surfactant wherein said hygro-scopic synthetic surfactant is selected from surfactants which absorb at least about 20% of their dry weight in water at 26-C and 80% Relative Humidity in three days.
WO 92/09679 2 0 9 5 3 5 1 14 - PCl'/US91/0873J
The above highly preferred personal cleansing bar is more preferred when said hygroscopic synthetic surfactant is selected from the group consisting of alpha sulfo fatty acid esters; alkyl sulfates; alkyl ether carboxylates; alkyl betaines; alkyl sul-taines; alkyl amine oxides; alkyl ether sulfates; and mixturesthereof.
This highly preferred personal cleansing bar is more pre-ferred when said bar contains from about 0.5% to about 40% of salts and/or salt hydrates selected from the group consisting of:
sodium chloride, sodium sulfate, disodium hydrogen phosphate, sodium pyrophosphate, sodium tetraborate, sodium acetate, sodium citrate, and other compatible salts of inorganic acids and short chain organic acids.
A highly preferred cleansing bar comprises: various combi-nations of the core structure of sodium soap fibers, water, mildsynthetic surfactants, bar appearance stabilizers, skin mildness aides and other cleansing bar adjuvants. Such preferred bar can be formulated to have essentially no bar smear.
Some preferred bars of the present invention comprise: a rigid, interlocking mesh of neutralized carboxylic acid fiber-like core consisting essentially of sodium fatty acid soap composed of at least 50% saturated fatty alkyl chains having 12 to 24 carbon atoms. Preferably at least about 25% of said saturated alkyl chains are of a single chain length.
Some compositions of this invention comprise the above-defined rigid mesh with water and without water. These compo-sitions must be formed with water or another suitable solvent system. The compositions can be made with large amounts of water and the water level in the final composition can be reduced to as low as about 1% or 2%.
However, it is a special advantage of some structures de-scribed herein that they can be dehydrated without loss of the integrity of the mesh. Some preferred shaped solids can be dehydrated without appreciable change in their outer dimensions.
Other bars shrink while maintaining their three-dimensional form.
Some bars herein have the unique characteristic that they are not destroyed by dehydration.
W O 92/09679 P ~ /US91/08733 More complex bars of the present invention comprise a skele-tal structure comprising other salts of fatty acids selected from potassium, magnesiumt triethanolammonium and/or calcium soaps used in combination with the selected levels of sodium and/or lithium soaps. More complex cleansing bars can contain surprisingly large amounts of water, mild synthetic surfactants, bar appearance stabilizers, skin mildness aids and other cleansing bar adjuvants;
yet are mild and have very good low smear.
Tables 1-3 set out some preferred bars which are made with the sodium salts of the fatty carboxylic acid (FA) soap.
The percentages, ratios, and parts herein are on a total composition weight basis, unless otherwise specified. All levels and ranges herein are approximations unless otherwise specified.
TABLE l 15Preferred Bars~ Chain Lenqths and Levels More Most Preferred Preferred Preferred Water Level 15-94% 25-60% 30-45%
Water:Soap Ratio 0.7:1 1:1-5:1 1.5:1-2:1 FA Chain Length Cl2-24 Cl4-22 Cl4-l8 FA Soap Level in Total Formulation 6-50% 15-35% 15-30%
All highs and lows are not necessarily shown in Table 1. For example, some selected sodium soap can be used at a level up to about 75%. Thus, the range is from about 5% to about 75%. The preferred levels and ratios can vary from cation to cation, etc., and from mono- to polycarboxylic acids.
The bars shown in Table 1 are made with the level of water indicated, but the water level of the final bars can be reduced to provide bars which contain reduced levels of water or even little or no water. A preferred level of water is from about 20% to about 80% by weight of the bar.
Table 2 below shows some preferred levels of soaps of a single FA chain length. Table 3 shows some preferred levels of unsaturation in the FA's used in the compositions of the present WO 92/09679 2 o 9 5 3 5 1 - ! ~ PCI/US91/08733 invention. Some preferred compositions contain little or no short chain FA's of ten carbon atoms or less. The terms "soap", "fatty acid (FA) salts" and "monocarboxylic acid salts" as used herein are sometimes interchangeable. "Soap" is used since it is easier to relate to and is the preferred embodiment.
The % SoaD of Single Chain Lenqth (of Total Fibrous SoaD Content) More Most Preferred Preferred Preferred Cl2-24 25-100% 50-100% 75-100%
The Total % Unsaturated or Low (C1o or less) Chain Lenqth SoaDs More Broad Preferred Preferred Cl2 0-15% 0-5% 0-1%
C14-24 0-50% 0-10% 0-1%
The highs and lows of some key preferred optional ingredients for complex soap bar compositions of this invention are set out in Table 4. None of these ingredients is essential for the basic, preferred bar core structure. Zero is the lowest level for each optional ingredient. Some preferred bars can contain a total of from about 0.1% up to about 70% of such ingredients. The idea here is that the core bars can contain large amounts of other ingredients besides soap and water. The levels set out in Table 4 are particularly illustrative for bars containing from more than 5% to about 75% selected sodium soap and other ingredients.
It should be understood that solid shapes can be made with just lithium soap or just neutralized polycarboxylic acid, but would be expected to be somewhat different from the levels and ratios given for sodium soaps.
WO 92/096792 ~ 9 5 3 5 1 ~ ! ~ PCI'/US91 /08733 Hiqhs and Lows Wt.% of Other Inqredients for More ComDlex Sodium Soa~ Bars More Most 5Preferred Preferred Preferred Neutralized Dicar-boxylic Acid 1-40% 2-30% 5-25%
Lithium "Soap" 1-40% 2-30% 5-25%
Potassium Soap 1-10% 2-10% 5-8%
Magnesium or Calcium Soap 1-35% 1-12% 3-8%
Triethanolammonium Soap 1-15% 2-15% 5-10%
Synthetic Surfactant 1-60% 4-25% 8-16%
Other Salts and Salt Hydrates 0.5-50% 1-25% 2-15%
Non-Volatile, Water-Soluble Nonionic Organics 1.0-50% 2-40% 5-20%
Polymeric Mildness Enhancers 0.1-20% 0.25-10% 1-5%
Waxes 0.1-40% 2-35% 3-10%
Other Impalpable Water-insolubles 1-60% 4-25% 8-16%
Aluminosilicates/Clay 0.5-25% 1-10% 3-8%
The soaps useful in the present invention can be of the same alkyl chain lengths, i.e., which are selected from the 12 to 24 carbon atoms as set out in Table 2. The same chain lengths apply for the other non-sodium soaps used in the bars of the present invention.
The sodium soap is preferably at least about 50% of the soap present in the bar.
The levels of potassium soap and/or triethanolammonium soap should not exceed one-half, preferably one-third, more preferably less than one-fourth, that of the sodium soap and the level of -magnesium soap should not exceed about one-third of the level of sodium soap, and is preferably less than about one-fourth that of the sodium soap.
-- 18 ~ 3 ~ ~
The total of other soaps, save lithium soap, should preferably not exceed one-half, preferably one-third, of the sodium soap.
The synthetic detergent constituent of the bar compositions of the invention can be designated as being a detergent from the class consisting of anionic, nonionic, amphoteric and zwitterionic synthetic detergents. Both low and high lathering and high and low water-soluble surfactants can be used in the bar compositions of the present invention.
Examples of suitable synthetic detergents for use herein are those described in U.S. Pat. No. 3,351,558, Zimmerer, issued Nov. 7, 1967, at column 6, line 70 to column 7, line 74.
Examples include the water-soluble salts of organic, sulfonic a~k~
and of aliphatic sulfuric acid esters, that is, water-soluble salts of organic sulfuric reaction products having in the molecular structure an alkyl radical of from 10 to 22 carbon atoms and a radical selected from the group consisting of sulfonic acid and sulfuric acid ester radicals.
Synthetic sulfate detergents of special interest are the normally solid alkali metal salts of sulfuric acid esters of normal primary aliphatic alcohols having from 10 to 22 carbon atoms. Thus, the sodium and potassium salts of alkyl sulfuric acids obtained from the mixed higher alcohols derived by the reduction of tallow or by the reduction of coconut oil, palm oil, stearine, palm kernel oil, babassu kernel oil or other oils of the coconut group can be used herein.
Other aliphatic sulfuric acid esters which can be suitably employed include the water-soluble salts of sulfuric acid esters of polyhydric alcohols incompletely esterified with high molecular weight soap-forming carboxylic acids. Such synthetic detergents include the water-soluble alkali metal salts of sulfuric acid esters of higher molecular weight fatty acid monoglycerides such as the sodium and potassium salts of the coconut oil fatty acid monoester of 1,2-hydroxy-propane-3-sulfuric acid ester, sodium and potassium monomyristoyl ethylene glycol sulfate, and sodium and potassium monolauroyl diglycerol sulfate.
B
-The synthetic surfactants and other optional materials useful in conventional cleaning products are also useful in the present invention. In fact, some ingredients such as certain hygroscopic synthetic surfactants which are normally used in liquids and which are very difficult to incorporate into 5 normal cleansing bars are very compatible in the bars of the present invention. Thus, essentially all of the known synthetic surfactants which are useful in cleansing products are useful in the compositions of the present invention. The cleansing product patent literature is full of synthetic surfactant disclosures. Some preferred surfactants as well as other cleansing product ingredients are disclosed in the following references:
Pat. No. Issue Date Inventor(s) 4,061,602 12/1977 Oberstar et al.
4,234,464 11/1980 Morshauser 4,472,297 9/1984 Bolich et al.
4,491,539 1/1985 Hoskins et al.
4,540,507 9/1985 Grollier 4,565,647 1/1986 Ll enado 4,673,525 6/1987 Small et al.
4,704,224 11/1987 Saud 4,788,006 11/1988 Bolich, Jr., et al.
4,812,253 3/1989 Small et al.
4,820,447 4/1989 Medcalf et al.
4,906,459 3/1990 Cobb et al.
4,923,635 5/1990 Simion et al.
4,954,282 9/1990 Rys et al.
Some preferred synthetic surfactants are shown the Examples herein. Preferred synthetic surfactant systems are selectively designed for bar appearance stability, lather, cleansing and mildness.
It is noted that surfactant mildness can be measured by a skin barrier 30 destruction test which is used to assess the irritancy potential ofsurfactants. In this test the milder the surfactant, the lesser the skin barrier is destroyed. Skin barrier destruction is measured by the relative amount of radio-labeled water (3H-H2o) which passes from the test solution through the skin epidermis into the physiological buffer contained in the B
3 ~ ~1 diffusate chamber. This test is described by T.J. Franz in the J. Invest.
Dermatol., 1975, 64, pp. 190-195; and in U.S. Pat. No. 4,673,525, Small et al., issued June 16, 1987, and which disclose a mild alkyl glyceryl ether sulfonate (AGS) surfactant based synbar comprising a "standard" alkyl glyceryl ether sulfonate mixture. Barrier destruction testing is used to select mild surfactants. Some preferred mild synthetic surfactants are disclosed in the above Small et al. patents and Rys et al. Some specific examples of preferred surfactants are used in the Examples herein.
Some examples of good lather enhancing detergent surfactants, mild ones, are e.g., sodium lauroyl sarcosinate, alkyl glyceryl ether sulfonate, sulfonated fatty esters, paraffin sulfonates, and sulfonated fatty acids.
Numerous examples of other surfactants are disclosed in the above patents. They include other alkyl sulfates, anionic acyl sarcosinates, methyl acyl taurates, N-acyl glutamates, acyl isethionates, alkyl sulfosuccinates, alkyl phosphate esters, ethoxylated alkyl phosphate esters, trideceth sulfates, protein condensates, mixtures of ethoxylated alkyl sulfates and alkyl amine oxides, betaines, sultaines, and mixtures thereof. Included in the surfactants are the alkyl ether sulfates with 1 to 12 ethoxy groups, especially ammonium and sodium lauryl ether sulfates.
Alkyl chains for these other surfactants are C8-C22, preferably C10-Cl8.
Alkyl glycosides and methyl glucose esters are preferred mild nonionics which may be mixed with other mild anionic or amphoteric surfactants in the compositions of this invention. Alkyl polyglycoside detergents are useful lather enhancers. The alkyl group can vary from about 8 to about 22 and the glycoside units per molecule can vary from about 1.1 to about 5 to provide an appropriate balance between the hydrophilic and hydrophobic portions of the molecule. Combinations of C8-Cl8, preferably Cl2-Cl6, alkyl polyglycosides withaverage degrees of glycosidation ranging from about 1.1 to about 2.7, preferably from about 1.2 to about 2.5, are preferred.
W O 92/09679 2 0 9 5 3 S 1 - PC~r/US91/08733 Sulfonated esters of fatty esters are preferred wherein the chain length of the carboxylic acid is C8-c227 preferably C12-C18;
the chain length of the ester alcohol is Cl-C6. These include sodium alpha sulfomethyl laurate, sodium alpha sulfomethyl coco-ate, and sodium alpha sulfomethyl tallowate.
Amine oxide detergents are good lather enhancers. Some preferred amine oxides are Cg-Clg, preferably Clo-C16, alkyl dimethyl amine oxides and Cg-Clg, preferably C12-C16, fatty acyl amidopropyl dimethyl amine oxides and mixtures thereof.
Fatty acid alkanolamides are good lather enhancers. Some preferred alkanolamides are Cg-C1g, preferably C12-C16, mono-ethanolamides, diethanolamides, and monoisopropanolamides and mixtures thereof.
Other detergent surfactants are alkyl ethoxy carboxylates having the general formula RO(CH2CH20JkCH2COO-M+
wherein R is a Cg 22 alkyl group, k is an integer ranging from O
to 10, and M is a cation; and polyhydroxy fatty acid amides having the general formula o R1 ll I
wherein Rl is H, a C1 4 alkyl group, 2-hydroxy ethyl, 2-hydroxy propyl, or mixtures thereof, R2 is a Cs 31 hydrocarbyl, and Z is a polyhydroxyhydrocarbyl having a linear hydrocarbyl chain with at least 3 hydroxyl groups directly connected to the chain, or an alkoxylated derivative thereof.
Betaines are good lather enhancers. Betaines such as Cg-C1g, preferably C12-C16, alkyl betaines, e.g., coco betaines or Cg-Clg, preferably C12-C16, acyl amido betaines, e.g., cocoamidopropyl betaine, and mixtures thereof, are preferred.
Some of the preferred surfactants are hygroscopic synthetic surfactants which absorb at least about 20% of their dry weight at 26~C and 80% relative humidity in three days. Hygroscopic sur-factants help to improve bar lather. Some preferred hygroscopicsynthetic surfactants are listed below. Note that all are not hygroscopic.
~ . ! .
W O 92/09679 2 0 9 ~3 51 22 - P~/US91/08733 HYqroscoDicity of Some Surfactants The hygroscopic surfactants are defined herein as having a minimum of 20% total moisture gain after 3 days at 26-C and 80%
Relative Humidity.
C1ass: Nonionic Sulfonates Total % Moisture Pick-Up*
Sodium C8 Glyceryl Ether Sulfonate 39.8 Sodium C12 14 Glyceryl Ether Sulfonate 22.9 Sodium C16 Glyceryl Ether Sulfonate 71.4 Sodium Cocomonoglyceride Sulfonate 3.5 Sodium Salt of Cg 16 Alkyl Glyceryl Ether Sulfonates AlDha Sulfo Esters and Acids Total % Moisture Pick-UD*
Sodium Alpha Sulfo Methyl Laurate/Myristate 39.3 Sodium Alpha Sulfo Methyl Myristate44.5 Sodium Alpha Sulfo Hexyl Laurate 23.2 Sodium Alpha Sulfo Methyl/Hexyl Laurate and Myristate 26.3 Sodium Alpha Sulfo Methyl Palmitate 3.7 Sodium Alpha Sulfo Methyl Stearate 4.2 Sodium 2-Sulfo Lauric Acid 0.2 Sodium 2-Sulfo Palmitic Acid 3.8 Sodium 2-Sulfo Stearic Acid 0.0 Na+Rl-C(s03-)-co2R2 Rl = C8-14 alkyl; R2 = Cl 8 alkyl Sodium Alkvl IsethionatesTotal % Moisture Pick-UP*
Sodium Lauryl Isethionate 31.7 Sodium Cocoyl Isethionate 11.0 Sarcosinates Total % Moisture Pick-UD*
Sodium Lauryl Sarcosinate 8.8 Sodium Stearyl Sarcosinate 13.3 Sodium Cocoyl Sarcosinate 18.7 W O 92/09679 2 0 9 5 ~ 5 1 P~/US91/08733 AlkYl Sulfates Total ~O Moisture Pick-UP*
Sodium Lauryl Sulfate 28.2 Sodium Laureth-1 Sulfate 37.6 Sodium Oleyl Sulfate 20.3 Sodium Cetearyl Sulfate 4.7 Sodium Cetyl Sulfate 2.25 Na+R1(OCH2CH2)nOS03~ R1 = C8 14 alkyl, C16 20 alkyl(ene) with at least one double bond, n = 0-18 ACY1 Glutamates Total % Moisture Pick-UP*
Sodium Cocoyl Glutamate 26.7 Sodium Lauryl Glutamate 17.8 Sodium Myristyl Glutamate 18.1 Sodium Stearyl Glutamate 12.0 AlkYl Ether CarboxYlates Total % Moisture Pick-UP*
Sodium Laureth-5 Carboxylate 32.2 Sodium Palmityl-20 Carboxylate 50.2 Na+R1-(0-CH2CH2)nc02- R1 = Cg 18 alkyl, n = 1-30 Sulfosuccinates Total % Moisture Pick-UP*
Disodium Laureth Sulfosuccinate33.6 PhosDhates Total % Moisture Pick-UP*
Sodium Monoalkyl (70% C12/30% C14) Phosphate 21.1 Class: AmDhoterics Betaines Total ~/O Moisture Pick-UP*
Coco Betaine 70.0 Cocoamidopropyl Betaine 48.2 Palmitylamidopropyl Betaine 46.5 Isostearamidopropyl Betaine 44.3 r ~ P
3 ~
Sultaines Total % Moisture Pick-Up*
Cocoamidopropylhydroxy Sultaine 59.5 Amine Oxides Total % Moisture Pick-Up*
Palmityl Dimethyl Amine Oxide 34.0 Myristyl Dimethyl Amine Oxide 46.0 Cocoamidopropyl Amine Oxide 43.3 Protein Derived Total % Moisture Pick-Up*
Na/TEA C12 Hydrolyzed Keratin 34.7 *3 days, 26~C/80% Relative Humidity Polymeric skin mildness aids are disclosed in the Small et al. and Medcalf et al. patents. Both cationic polysaccharides and cationic synthetic polymers are disclosed. The cationic synthetic polymers useful in the present invention are cationic polyalkylene imines, ethoxypolyalklene imines, and poly[N-[-3-(dimethylammonio)-propyl]-N'-[3-(ethyleneoxyethylene dimethylammonio)propyl]urea dichloride] thelatter of which is available from Miranol Chemical Company, Inc. under the trademark of Miranol A-15, CAS Reg. No. 68555-36-2.
Preferred cationic polymeric skin conditioning agents of the present invention are those cationic polysaccharides of the cationic guar gum class with molecular weights of 1,000 to 3,000,000. More preferred molecular weights are from 2,500 to 350,000. These polymers have a polysaccharide backbone comprised of galactomannan units and a degree of cationic substitution ranging from about 0.04 per anhydroglucose unit to about 0.80 per anhydroglucose unit with the substituent cationic group being the adduct of 2,3-epoxypropyltrimethyl ammonium chloride to the natural polysaccharide backbone. Examples are JAGUAR~ C-14-S, C-15 and C-17 sold by Celanese Corporation. In order to achieve the benefits described in this invention, the polymer must have characteristics, either structural or physical which allow it to be suitable and fully hydrated and subsequently well incorporated into the soap matrix.
- 25 - 2 ~ ~ 5 3 ~ ~
A mild skin cleansing bar of the present invention can contain from about 0.5% to about 20% of a mixture of a silicone gum and a silicone fluid wherein the gum:fluid ratio is from about 10:1 to about 1:10, preferably from about 4:1 to about 1:4, most preferably from about 3:2 to about 2:3.
Silicone gum and fluid blends have been disclosed for use in shampoos and/or conditioners in U.S. Pat. Nos. 4,906,459, Cobb et al., issued March 6, 1990; 4,788,006, Bolich, Jr. et al., issued Nov. 29, 1988; 4,741,855, Grote et al., issued May 3, 1988; 4,728,457, Fieler et al., issued March 1, 1988;
Dermatol., 1975, 64, pp. 190-195; and in U.S. Pat. No. 4,673,525, Small et al., issued June 16, 1987, and which disclose a mild alkyl glyceryl ether sulfonate (AGS) surfactant based synbar comprising a "standard" alkyl glyceryl ether sulfonate mixture. Barrier destruction testing is used to select mild surfactants. Some preferred mild synthetic surfactants are disclosed in the above Small et al. patents and Rys et al. Some specific examples of preferred surfactants are used in the Examples herein.
Some examples of good lather enhancing detergent surfactants, mild ones, are e.g., sodium lauroyl sarcosinate, alkyl glyceryl ether sulfonate, sulfonated fatty esters, paraffin sulfonates, and sulfonated fatty acids.
Numerous examples of other surfactants are disclosed in the above patents. They include other alkyl sulfates, anionic acyl sarcosinates, methyl acyl taurates, N-acyl glutamates, acyl isethionates, alkyl sulfosuccinates, alkyl phosphate esters, ethoxylated alkyl phosphate esters, trideceth sulfates, protein condensates, mixtures of ethoxylated alkyl sulfates and alkyl amine oxides, betaines, sultaines, and mixtures thereof. Included in the surfactants are the alkyl ether sulfates with 1 to 12 ethoxy groups, especially ammonium and sodium lauryl ether sulfates.
Alkyl chains for these other surfactants are C8-C22, preferably C10-Cl8.
Alkyl glycosides and methyl glucose esters are preferred mild nonionics which may be mixed with other mild anionic or amphoteric surfactants in the compositions of this invention. Alkyl polyglycoside detergents are useful lather enhancers. The alkyl group can vary from about 8 to about 22 and the glycoside units per molecule can vary from about 1.1 to about 5 to provide an appropriate balance between the hydrophilic and hydrophobic portions of the molecule. Combinations of C8-Cl8, preferably Cl2-Cl6, alkyl polyglycosides withaverage degrees of glycosidation ranging from about 1.1 to about 2.7, preferably from about 1.2 to about 2.5, are preferred.
W O 92/09679 2 0 9 5 3 S 1 - PC~r/US91/08733 Sulfonated esters of fatty esters are preferred wherein the chain length of the carboxylic acid is C8-c227 preferably C12-C18;
the chain length of the ester alcohol is Cl-C6. These include sodium alpha sulfomethyl laurate, sodium alpha sulfomethyl coco-ate, and sodium alpha sulfomethyl tallowate.
Amine oxide detergents are good lather enhancers. Some preferred amine oxides are Cg-Clg, preferably Clo-C16, alkyl dimethyl amine oxides and Cg-Clg, preferably C12-C16, fatty acyl amidopropyl dimethyl amine oxides and mixtures thereof.
Fatty acid alkanolamides are good lather enhancers. Some preferred alkanolamides are Cg-C1g, preferably C12-C16, mono-ethanolamides, diethanolamides, and monoisopropanolamides and mixtures thereof.
Other detergent surfactants are alkyl ethoxy carboxylates having the general formula RO(CH2CH20JkCH2COO-M+
wherein R is a Cg 22 alkyl group, k is an integer ranging from O
to 10, and M is a cation; and polyhydroxy fatty acid amides having the general formula o R1 ll I
wherein Rl is H, a C1 4 alkyl group, 2-hydroxy ethyl, 2-hydroxy propyl, or mixtures thereof, R2 is a Cs 31 hydrocarbyl, and Z is a polyhydroxyhydrocarbyl having a linear hydrocarbyl chain with at least 3 hydroxyl groups directly connected to the chain, or an alkoxylated derivative thereof.
Betaines are good lather enhancers. Betaines such as Cg-C1g, preferably C12-C16, alkyl betaines, e.g., coco betaines or Cg-Clg, preferably C12-C16, acyl amido betaines, e.g., cocoamidopropyl betaine, and mixtures thereof, are preferred.
Some of the preferred surfactants are hygroscopic synthetic surfactants which absorb at least about 20% of their dry weight at 26~C and 80% relative humidity in three days. Hygroscopic sur-factants help to improve bar lather. Some preferred hygroscopicsynthetic surfactants are listed below. Note that all are not hygroscopic.
~ . ! .
W O 92/09679 2 0 9 ~3 51 22 - P~/US91/08733 HYqroscoDicity of Some Surfactants The hygroscopic surfactants are defined herein as having a minimum of 20% total moisture gain after 3 days at 26-C and 80%
Relative Humidity.
C1ass: Nonionic Sulfonates Total % Moisture Pick-Up*
Sodium C8 Glyceryl Ether Sulfonate 39.8 Sodium C12 14 Glyceryl Ether Sulfonate 22.9 Sodium C16 Glyceryl Ether Sulfonate 71.4 Sodium Cocomonoglyceride Sulfonate 3.5 Sodium Salt of Cg 16 Alkyl Glyceryl Ether Sulfonates AlDha Sulfo Esters and Acids Total % Moisture Pick-UD*
Sodium Alpha Sulfo Methyl Laurate/Myristate 39.3 Sodium Alpha Sulfo Methyl Myristate44.5 Sodium Alpha Sulfo Hexyl Laurate 23.2 Sodium Alpha Sulfo Methyl/Hexyl Laurate and Myristate 26.3 Sodium Alpha Sulfo Methyl Palmitate 3.7 Sodium Alpha Sulfo Methyl Stearate 4.2 Sodium 2-Sulfo Lauric Acid 0.2 Sodium 2-Sulfo Palmitic Acid 3.8 Sodium 2-Sulfo Stearic Acid 0.0 Na+Rl-C(s03-)-co2R2 Rl = C8-14 alkyl; R2 = Cl 8 alkyl Sodium Alkvl IsethionatesTotal % Moisture Pick-UP*
Sodium Lauryl Isethionate 31.7 Sodium Cocoyl Isethionate 11.0 Sarcosinates Total % Moisture Pick-UD*
Sodium Lauryl Sarcosinate 8.8 Sodium Stearyl Sarcosinate 13.3 Sodium Cocoyl Sarcosinate 18.7 W O 92/09679 2 0 9 5 ~ 5 1 P~/US91/08733 AlkYl Sulfates Total ~O Moisture Pick-UP*
Sodium Lauryl Sulfate 28.2 Sodium Laureth-1 Sulfate 37.6 Sodium Oleyl Sulfate 20.3 Sodium Cetearyl Sulfate 4.7 Sodium Cetyl Sulfate 2.25 Na+R1(OCH2CH2)nOS03~ R1 = C8 14 alkyl, C16 20 alkyl(ene) with at least one double bond, n = 0-18 ACY1 Glutamates Total % Moisture Pick-UP*
Sodium Cocoyl Glutamate 26.7 Sodium Lauryl Glutamate 17.8 Sodium Myristyl Glutamate 18.1 Sodium Stearyl Glutamate 12.0 AlkYl Ether CarboxYlates Total % Moisture Pick-UP*
Sodium Laureth-5 Carboxylate 32.2 Sodium Palmityl-20 Carboxylate 50.2 Na+R1-(0-CH2CH2)nc02- R1 = Cg 18 alkyl, n = 1-30 Sulfosuccinates Total % Moisture Pick-UP*
Disodium Laureth Sulfosuccinate33.6 PhosDhates Total % Moisture Pick-UP*
Sodium Monoalkyl (70% C12/30% C14) Phosphate 21.1 Class: AmDhoterics Betaines Total ~/O Moisture Pick-UP*
Coco Betaine 70.0 Cocoamidopropyl Betaine 48.2 Palmitylamidopropyl Betaine 46.5 Isostearamidopropyl Betaine 44.3 r ~ P
3 ~
Sultaines Total % Moisture Pick-Up*
Cocoamidopropylhydroxy Sultaine 59.5 Amine Oxides Total % Moisture Pick-Up*
Palmityl Dimethyl Amine Oxide 34.0 Myristyl Dimethyl Amine Oxide 46.0 Cocoamidopropyl Amine Oxide 43.3 Protein Derived Total % Moisture Pick-Up*
Na/TEA C12 Hydrolyzed Keratin 34.7 *3 days, 26~C/80% Relative Humidity Polymeric skin mildness aids are disclosed in the Small et al. and Medcalf et al. patents. Both cationic polysaccharides and cationic synthetic polymers are disclosed. The cationic synthetic polymers useful in the present invention are cationic polyalkylene imines, ethoxypolyalklene imines, and poly[N-[-3-(dimethylammonio)-propyl]-N'-[3-(ethyleneoxyethylene dimethylammonio)propyl]urea dichloride] thelatter of which is available from Miranol Chemical Company, Inc. under the trademark of Miranol A-15, CAS Reg. No. 68555-36-2.
Preferred cationic polymeric skin conditioning agents of the present invention are those cationic polysaccharides of the cationic guar gum class with molecular weights of 1,000 to 3,000,000. More preferred molecular weights are from 2,500 to 350,000. These polymers have a polysaccharide backbone comprised of galactomannan units and a degree of cationic substitution ranging from about 0.04 per anhydroglucose unit to about 0.80 per anhydroglucose unit with the substituent cationic group being the adduct of 2,3-epoxypropyltrimethyl ammonium chloride to the natural polysaccharide backbone. Examples are JAGUAR~ C-14-S, C-15 and C-17 sold by Celanese Corporation. In order to achieve the benefits described in this invention, the polymer must have characteristics, either structural or physical which allow it to be suitable and fully hydrated and subsequently well incorporated into the soap matrix.
- 25 - 2 ~ ~ 5 3 ~ ~
A mild skin cleansing bar of the present invention can contain from about 0.5% to about 20% of a mixture of a silicone gum and a silicone fluid wherein the gum:fluid ratio is from about 10:1 to about 1:10, preferably from about 4:1 to about 1:4, most preferably from about 3:2 to about 2:3.
Silicone gum and fluid blends have been disclosed for use in shampoos and/or conditioners in U.S. Pat. Nos. 4,906,459, Cobb et al., issued March 6, 1990; 4,788,006, Bolich, Jr. et al., issued Nov. 29, 1988; 4,741,855, Grote et al., issued May 3, 1988; 4,728,457, Fieler et al., issued March 1, 1988;
4,704,272, Oh et al., issued Nov. 3, 1987; and 2,826,551, Geen, issued March 11, 1958.
The silicone component can be present in the bar at a level which is effective to deliver a skin mildness benefit, for example, from about 0.5% to about 20%, preferably from about 1.5% to about 16%, and most preferably from about 3% to about 12% of the composition. Silicone fluid, as used herein, denotes a silicone with viscosities ranging from about 5 to about 600,000 centistokes, most preferably from about 350 to about 100,000 centistokes, at 25~C. Silicone gum, as used herein, denotes a silicone with a mass molecular weight of from about 200,000 to about 1,000,000 and with a viscosity of greater than about 600,000 centistokes. The molecular weight and viscosity of the particular selected siloxanes will determine whether it is a gum or a fluid. The silicone gum and fluid are mixed together and incorporated into the compositions of the present invention.
Other ingredients of the present invention are selected for the various applications. E.g., perfumes can be used in formulating the skin cleansing products, generally at a level of from about 0.1% to about 2.0% of the composition. Alcohols, hydrotropes, colorants, and fillers such as talc, clay, water-insoluble, impalpable calcium carbonate and dextrin can also be used. Cetearyl alcohol is a mixture of cetyl and stearyl alcohols.
Preservatives, e.g., sodium ethylene-diaminetetraacetate (EDTA), generally at a level of less than 1% of the composition, can be incorporated in the cleansing products to prevent color and odor degradation.
Antibacterials can also be incorporated, usually at B
2o9l53,sl ~
WO 92/09679 I ~ P~/US91/08733 levels up to 1.5%. The above patents disclose or refer to such ingredients and formulations which can be used in the bars of this invention, and are incorporated herein by reference.
Some bars of this invention contain from about more than 5%
The silicone component can be present in the bar at a level which is effective to deliver a skin mildness benefit, for example, from about 0.5% to about 20%, preferably from about 1.5% to about 16%, and most preferably from about 3% to about 12% of the composition. Silicone fluid, as used herein, denotes a silicone with viscosities ranging from about 5 to about 600,000 centistokes, most preferably from about 350 to about 100,000 centistokes, at 25~C. Silicone gum, as used herein, denotes a silicone with a mass molecular weight of from about 200,000 to about 1,000,000 and with a viscosity of greater than about 600,000 centistokes. The molecular weight and viscosity of the particular selected siloxanes will determine whether it is a gum or a fluid. The silicone gum and fluid are mixed together and incorporated into the compositions of the present invention.
Other ingredients of the present invention are selected for the various applications. E.g., perfumes can be used in formulating the skin cleansing products, generally at a level of from about 0.1% to about 2.0% of the composition. Alcohols, hydrotropes, colorants, and fillers such as talc, clay, water-insoluble, impalpable calcium carbonate and dextrin can also be used. Cetearyl alcohol is a mixture of cetyl and stearyl alcohols.
Preservatives, e.g., sodium ethylene-diaminetetraacetate (EDTA), generally at a level of less than 1% of the composition, can be incorporated in the cleansing products to prevent color and odor degradation.
Antibacterials can also be incorporated, usually at B
2o9l53,sl ~
WO 92/09679 I ~ P~/US91/08733 levels up to 1.5%. The above patents disclose or refer to such ingredients and formulations which can be used in the bars of this invention, and are incorporated herein by reference.
Some bars of this invention contain from about more than 5%
5 to about 75% said sodium fatty acid soap fibers; from about 10% to about less than 94% water; and at least about 1% of another bar ingredient selected from: other soaps, moisturizers, colorants, solvents, fillers, synthetic detergent surfactants, polymeric skin feel and mildness aids, perfumes, preservatives, and mixtures thereof.
Some bars of this invention comprise: more than 5% to 50%
fibrous sodium fatty acid soap composed of at least about 50%
saturated fatty alkyl chains having 12-24 carbon atoms of which at least about 25% of said saturated fatty alkyl chains is of a 15 S i ngle chain length.
Some bars of this invention comprise said fibers which occupy from about 3% to about 75%, preferably from about 15% to about 40%, of the volume of the bar structure.
Some bars comprise a rigid, low smearing structure of: more 20 than 5% to 75% sodium fatty acid soap composed of at least about 50% saturated fatty alkyl chains having 12-24 carbon atoms of which at least about 25% of said saturated fatty alkyl chains is of a single chain length; from about 10% to about 94% water; and about 0% to a total of about 70% of other selected soap bar 25 ingredients selected from the group set out above in Table 4.
Some personal cleansing soap bar compositions comprise a rigid interlocked mesh of sodium soap fibers; wherein the sodium fatty acid soap is composed of at least about 50% saturated fatty alkyl chains having 12-24 carbon atoms of which at least about 25%
of said saturated fatty alkyl chains is of a single chain length;
and from about 2% to about 40% by weight of a hygroscopic synthet-ic surfactant wherein said hygroscopic synthetic surfactant is selected from surfactants which absorb at least about 20% of its dry weight in water at 26~C and 80% Relative Humidity in three '5 days.
W O 92/09679 2 0 9 S 3 5 1 PC~r/US91/08733 Bar ADDearance Aids Bar appearance (water-retaining and/or shrinkage prevention) aids are preferably selected from the group consisting of:
compatible salt and salt hydrates;
water-soluble organics such as polyols, urea;
aluminumosilicates and clays; and mixtures thereof, as set out above in Table 4.
Water-soluble organics are also used to stabilize the appear-ance of the bar soaps of the present invention. Some preferred water-soluble organics are propylene glycol, glycerine, ethylene glycol, sucrose, and urea, and other compatible polyols.
A particularly suitable water-soluble organic is propylene glycol. Other compatible organics include polyols, such as ethylene glycol or 1,7-heptane-diol, respectively the mono- and polyethylene and propylene glycols of up to about 8,000 molecular weight, any mono-Cl 4 alkyl ethers thereof, sorbitol, glycerol, glycose, diglycerol, sucrose, lactose, dextrose, 2-pentanol, l-butanol, mono- di- and triethanolammonium, 2-amino-1-butanol, and the like, especially the polyhydric alcohols.
The term "polyol" as used herein includes non-reducing sugar, e.g., sucrose. Sucrose will not reduce Fehling's solution and therefore is classified as a "non-reducing" disaccharide. Unless otherwise specified, the term "sucrose" as used herein includes sucrose, its derivatives, and similar non-reducing sugars and similar polyols which are substantially stable at a soap pro-cessing temperature of up to about 210-F (98-C), e.g., trialose, raffinose, and stachyose; and sorbitol, lactitol and maltitol.
Compatible salt and salt hydrates are used to stabilize the bar soap appearance via the retention of water. Some preferred salts are sodium chloride, sodium sulfate, disodium hydrogen phosphate, sodium pyrophosphate, sodium tetraborate.
Generally, compatible salts and salt hydrates include the sodium, potassium, magnesium, calcium, aluminum, lithium, and ammonium salts of inorganic acids and small (6 carbons or less) carboxylic or other organic acids, corresponding hydrates. and mixtures thereof, are applicable. The inorganic salts include chloride, bromide, sulfate, metasilicate, orthophosphate, pyro-phosphate, polyphosphate, metaborate, tetraborate, and carbonate. The organic salts include acetate, formate, methyl sulfate, and citrate.
Water-soluble amine salts can also be used. Monoethanolamine, diethanolamine, and triethanolammonium (TEA) chloride salts are preferred.
5Aluminosilicates and other clays are useful in the present invention.
Some preferred clays are disclosed in U.S. Pat. Nos. 4,605,509 and 4,274,975.
Other types of clays include zeolite, kaolinite, montmorillonite, attapulgite, illite, bentonite, and halloysite. Another preferred clay is kaolin.
10Waxes include petroleum based waxes (paraffin, microcrystalline, and petrolatum), vegetable based waxes (carnauba, palm wax, candelilla, sugarcane wax, and vegetable derived triglycerides) animal waxes (beeswax, spemaceti, wool wax, shellac wax, and animal derived triglycerides). mineral waxes (montar, ozokerite, and ceresin) and synthetic waxes (Fischer-Tropsch).
15A preferred wax is used in the Examples herein. A useful wax has a melting point (M.P.) of from about 120~F to about 185~F (49-85~C), preferably from about 125~F to about 175~F (52~-79~C). A preferred paraffin wax is a fully refined petroleum wax having a melting point ranging from about 130~F
to about 140~F (49~-60~C). This wax is odorless and tasteless and meets FDA
requirements for use as coatings for food and food packages. Such paraffins are readily available commercially. A very suitable paraffin can be obtained, for example, from The Standard Oil Company of Ohio under the trade mark Factowax R-133.
Other suitable waxes are sold by the National Wax Co. under the trade 25names of 9182 and 6971, respectively, having melting points of 131~F and 130~F(-55~C).
The paraffin preferably is present in the bar in an amount ranging from about 5X to about 20% by weight. The paraffin ingredient is used in the product to impart skin mildness, plasticity, firmness, and processability.
It also provides a glossy look and smooth feel to the bar.
The paraffin ingredient is optionally supplemented by a microcrystalline wax. A suitable microcrystalline wax has a melting point ranging, for example, from about 140-F (60-C) to about 185-F (85-C), preferably from about 145'F (62-C) to about 175-F (79-C). The wax preferably should meet the FDA requirements for food grade microcrystalline waxes. A very suitable micro-crystalline wax is obtained from Witco Chemical Company under the trade mark Multiwax X-145A. The microcrystalline wax preferabiy is present in the bar in an amount ranging from about 0.5% to about 5% by weight. The microcrystalline wax ingredient imparts pliability to the bar at room temperatures.
EXAMPLES
The following examples are illustrative and are not intended to limit the scope of the invention. Unneutralized or "free"
fatty acids, as used in the examples, are of the same chain lengths as those used to make the soaps, unless otherwise speci-fied. All levels and ranges, temperatures, results, etc., used herein, are approximations unless otherwise specified.
A Frame Process for Makinq the Bars of the Present Invention The cleansing bars in the Examples are made by the following procedure unless otherwise specified:
1. Fatty acid precursor, propylene glycol, sodium chloride, and water (excluding water coming in with other raw materials) are mixed and heated to 71'C.
2. Caustic solution (50% sodium hydroxide) is added and the mixture is stirred until smooth forming an aqueous molten liquid comprising from 15% to 94% water and from 5.5% to 75% soap (neutralized carboxylic acid). The temperature during neutralization of the molten liquid increases to -95-C.
3. Other ingredients are added preferably in the following order and the temperature is maintained at -88-C: coco betaine; sodium lauroyl sarcosinate; or sodium alpha-sulfo methyl cocoate; kaolin clay; or hydrated zeolite (synthetic sodium aluminosilicate); and paraffin.
Perfume is added last.
4. The molten liquid mixture is poured into shaped molds.
W O 92/09679 2 0 9 ~3 51 - 30 - P~/US91/08733 5. The molten liquid crystallizes (solidifies) on cooling to room temperature and the resultant bars are removed from the molds.
The bars of the examples are made using the above general procedure, unless otherwise specified.
It is important to note that, when the formulations which are used in the Examples of the present invention are subjected to a conventional plodding or freezer process very soft or no bars are formed. Example II is a very highly preferred overall bar.
Preferred Bars Ex. I Ex. IIEx. III Ex. IV
Ingredient (Wt.%) (Wt.%)(Wt.%) (Wt.~,') Na C14 Soap 20 20 - -Na C16 Soap - - 20 16 K C16 Soap - - - 4 Free Fatty Acid Sodium Lauroyl Sarcosinate 7 7 12 Sodium Alpha Sulfo Methyl Cocoate - - - 7 Coco Betaine 5 5 7 5 Sodium Chloride 3.0 3.0 3.0 3.0 Propylene Glycol 14.5 14.5 14.5 15.0 Hydrated Zeolite A
(Aluminosilicate) 4.0 4.0 Kaolin Clay 4.0 - 4.0 Paraffin (M.P.=55-C) 6.5 6.5 4.5 Perfume Water 37.25 37.25 31.95 36.25 Hardness (mm~ 5.5 6.4 4.2 5.1 Smear 9.5 9.0 8.5 8.5 ~escription of Testinq for ExamPles 35Bar Hardness Test 1. The hardness of a bar is determined by measuring at 25~C
the depth of penetration (in mm) into the bar of a 247 gram , ~ ~
; .
Standard Weighted Penetrometer Probe having a conically shaped needle attached to a 22.9 cm (9 inch) shaft weighing 47 grams with 200 grams on top of said shaft. A hardness measurement of 5 mm or less indicates a very hard bar; 5-10 mm indicates a moderately hard bar; 10-12 mm indicates a somewhat soft bar of marginal acceptance; and greater than 12 mm indicates a very soft bar that is unacceptable for most uses. This defines "hardness" as used herein unless otherwise specified.
Bar Smear Test 2. The smear grade is determined by a (1) placing a soap bar on a perch in a 1400 mm diameter circular dish; (2) adding 200 ml of room temperature water to the dish such that the bottom 3 mm of the bar is submerged in water; (3) letting the bar soak over-night (15 hours); (4) turn the bar over and grade qualitatively for the combined amount of smear, and characteristics of smear, depth of smear on a scale where 10 equals no smear, 8.0-9.5 equals low smear amount, 5.0-7.5 equals moderate smears similar to most marketed bars, and 4.5 or less equals very poor smear.
Commercial soap bars, e.g., SAFEGUARD~, ZEST~, IVORY~, and LAVA~, have smears of about 5, 6, 6, and 6, respectively. See Table 12 for more data.
Bar Shrinkaqe Test 3. Shrinkage is measured by placing a freshly made un-wrapped bar in a room that is held at 26~C and 15% relative humidity for one week. The amount of shrinkage from the original bar shape is determined on a qualitative scale where O indicates no shrinkage, + indicates slight shrinkage, ++ indicates moderate shrinkage, and +++ indicates great shrinkage.
In Tables 6 and 7, soap bars 1-10 are set out to show bar hardness, smear and shrinkage for C1o, Cl2~ C14, C16~ and C18 alkyl chain soaps as shown. The preferred alkyl chain soaps of the present invention are set out above in Tables l and 2.
The term "X." means that the example is a comparative example.
WO 92/09679 2 0 9 S3~1 32 PCI/US91/08733 Sinqle Saturated Chain Lenqth Sodium Soap/Water StudY
Ex.1 Ex.2 Ex.3 Ex.4 Ex.5 Ingredient Wt.% Wt.% Wt.% Wt.% Wt.%
Sodium Soap Free Fatty Acid 1.0 1.0 1.0 1.0 2.0 Excess Sodium Hydroxide Sodium Chloride 2.0 1.0 1.0 1.0 1.0 Water 64 65 65 65 64 Hardness (mm) 8.9 2.3 2.2 5.4 4.2 Smear 3 10 10 9.5 10.0 Shrinkage +++ +++ + 0 Note that Ex. 1 has a very poor smear, notwithstanding a hardness of 8.9 as the smear methodology dissolves away the soluble C1o soap.
Single Chain Lenqth Sodium SoaD/Water StudY
X.6 Ex.7 Ex.8 Ex.9 Ex.10 Ingredient Wt.% Wt.% Wt.% Wt.% Wt.~o Sodium Soap C18:1 33 Free Fatty Acid 1.0 - 2.0 1.0 Excess Sodium Hydroxide - 0.07 Sodium Chloride 1.0 1.0 1.0 1.0 1.0 Water 65 87 82.8 83 94 W O 92/09679 2 0 9 S 3 S 1 ' - P ~ /US91/08733 _ - 33 -Hardness (mm) ** 11.8 11.9 14.0 Smear 10.0 10.0 9.0 Shrinkage 0 +++ ++++ ++++
** Solid bar not formed due to too much unsaturated soap.
Example 10 has the rigid structure, but is not preferred as a cleaning bar because its hardness is 14.
BinarY Chain Lenqth Sodium SoaD/Water Study X.11 Ex.12 Ex.13 InqredientWt.% Wt.% Wt.%
Sodium Soap C10 - - 16.5 Cl2 16.5 - -C14 - 16.5 16.5 C1g:1 16.5 16.5 Free Fatty Acid 1.0 1.0 1.0 Excess Sodium Hydroxide Sodium Chloride 1.0 1.0 1.0 Water 65 65 65 Hardness (mm) ** 9.0 9.0 Smear 9.0 8.0 **Solid Bar not formed due to too much unsaturation combined with C12 soap.
W O 92/09679209 ~ 3Sl ~ P~/US91/08733 Binarv Saturated Chain Lenqth Sodium SoaD/Water Studv Ex.14 Ex.15 Ex.16 Inqredient Wt.% Wt.% Wt.%
Sodium Soap Cl2 16.5 C14 16.5 C16 - 16.5 10 C18 - 16.5 10 Free Fatty Acid 1.0 1.0 1.0 Sodium Chloride 1.0 1.0 1.0 Water 65 65 78 Hardness (mm) 2.8 4.5 7.3 Smear 9.5 10.0 10.0 Shrinkage 0 ++
Examples 12-16 are excellent bars of the present invention.
20ComDlex Chain Lenqth Sodium SoaD/Water Studv Ex.17 Ex.18 Ex.19 Inqredient Wt.% Wt.% Wt.%
Sodium Soap*
Emersol 132 - (33) (15) C8 0.56 C1o 0.64 Cl2 10.14 0.12 8.1 (8.0) C14 4.54 0.79 10.4 (10.0) C16 8.51 15.6 7.10 C17 0.76 0.76 0.35 Cl8 19.85 15.3 7.0 C20 - 0.26 0.12 Free Fatty Acid - 1.0 Sodium Chloride 1.1 1.0 1.0 Water 53.9 65 66 W O 92/09679 2 0 9 5 3 5 1 P ~ /US9l/08733 Hardness (mm) 7.6 4.7 5.8 Smear 9.5 10 9.5 Shrinkage + ++
*Composition by Chain Length, () indicate actual level of materials.
Examples 17-19 are made with more complex mixtures of soaps than the prior examples. They form very good bars of the present invention. They have little or no smear. Compare their hardness and smears with those made with conventional tallow and coconut soap shown in Table 11 .
ComPlex Chain Lenqth Sodium SoaD/Water StudY
X.20 X.21 X.22 Inqredient Wt.% Wt.% Wt.%
Sodium Soap*
Tallow (33) - (26.4) Coconut - (33) (6.6) C8 - 2.31 0.46 C10 - 2.0 0.40 C12 ~ 16.5 3.3 C14 1.0 5.94 4.95 Cl6 7.92 2.81 6.90 C18 0-5 - 0.40 C20 6.6 1.0 5.48 C14:1 0.33 - 0.26 C16:1 0.83 - 0.66 C1g:1 14.2 2.0 11.76 C1g:2 0.75 0.5 0-7 Free Fatty Acid 1.0 1.0 1.0 Sodium Chloride 1.0 1.0 1.0 Water 65 65 65 Hardness (mm) Soft 15.8 12.5 ~5 Smear Poor 3.0 5.0 *Composition by Chain Length, () indicate actual level of materials.
W O 92/09679 2 0 9 5 ~ S I 36 P~/US91/08733 These comparative examples, X.20, X.21, and X.22, do not form the rigid structure of the present invention. Note that they are made with the typical commercial soaps. They are soft soaps with terrible smears. Compare with Example 15 of the present invention ; which is made with 65% water and C16 and C1g saturated soap and forms a hard bar with no smear.
Example 23 is a bar of the present invention which contains more synthetic surfactant than soap. It has low smear and good lather. Example 24 is a bar of the present invention which contains polymer and other bar soap ingredients.
SYndet Bar ExamPle Inqredient Wt.%
Sodium Palmitate 20 Sodium Lauroyl Sarcosinate 9*
Sodium Laureth-3 Sulfate 7*
Sodium Cetearyl Sulfate 5*
Free Fatty Acid (Palmitic) Sodium Chloride 3 Propylene Glycol 14 Hydrated Zeolite A 3 Perfume Water 37 *Total 21% Synthetic Surfactant 20953~1 WO 92/09679 i P~/US91/08733 PolYmer-Containinq ExamDle Ingredient Wt.%
Sodium Palmitate 20 Sodium Alpha-Sulfo Methyl Cocoate 8. 7 Coco Betaine 4.65 Jaguar C376 1.5 Propylene Glycol 15 Kaolin Clay 5 Paraffin, (M.P.=55-C) 4.5 Sodium Chloride 3 Perfume Water 35.5 Examples 23 and 24 are similar to Example IV of Table 5.
Example 24 is a mild bar formulation with polymeric skin mildness aid.
Ex. 25 Ex. 26 Ex.27 Inqredient Wt.% Wt.% Wt.%
Lithium Myristate 33 Lithium Chloride 5 - -Disodium Salt of Dodecanedioic Acid - 20 20 Sodium Lauroyl Sarcosinate - - 5 Water 62 80 75 Penetration Values N/A N/A N/A
N/A = Not available For Example 25, the formulation is prepared by heating the fatty acid precursor to 71-C, separately adding lithium hydroxide to water, and then adding the fatty acid and lithium hydroxide solution together, mixing together for 30 minutes maintaining the 35 heat at least at 71-C, adding lithium chloride salt and stirring for an additional 5 minutes, then pouring into a mold and letting ...
.. ~ . D
",, f ' cool and solidify. A solid bar with excellent smear properties is formed.
For Examples 26 and 27, the diacid is melted (150-180~C) and a hot (90~C) caustic solution (two equivalents of NaOH) is added. The mixture is stirred for -5 minutes. For Example 27, the sodium lauroyl sarcosinate is predissolved in the caustic/water solution. The bar becomes solid on cooling, with further hardening occurring upon degradation, e.g., to about 35-40% water by weight of the bar.
Example 25 demonstrates the ability to form high moisture, firm and non-smearing bars without the need for sodium soap. Examples 26 and 27 demonstrate the ability to form a totally soap-free product and still obtain the relatively rigid intermeshed fiber structure.
Example 28 below is made by a freezer bar process disclosed in commonly assigned, Canadian Pat. Application Ser. No. 2,113,564, Taneri et al. This process provides a personal cleansing freezer bar comprising a skeleton structure having a relatively rigid, interlocking, semi-continuous, open, three-dimensional, crystalline mesh of neutralized carboxylic acid soap made by the following steps:
(1) mixing a molten mixture comprising by weight of said bar:
20from about 15% to about 85% of said soap and from about 15%
to about 40% water;
(2) cooling said mixture to a semi-solid in a scraped wall heat exchanger freezer;
(3) extruding said semi-solid as a soft plug; and 25(4) further cooling and crystallizing said soft plug until firm to provide said personal cleansing freezer bar.
Step 1 - Mixinq The soap specified in the formulation is made in situ by mixing the desired fatty acids, consisting essentially of C12-C24 chain lengths, with the appropriate base or mixture of bases, consisting essentially of sodium, lithium, magnesium, calcium, and potassium hydroxide and triethanolamine. The fatty acid, base, and water are mixed at from about 170~F to about 200~F (76~-93~) 209~3~1 WO 92/09679 PCI'/US91/08733 - 3g -to form the soap. In Example 28, 180-F is used. Sufficient water is used such that the mixture is stirrable. The other ingredients are added, maintaining the temperature of from about 180-F to about 200-F (82--93-C). Example 28 - 180-F. The optimal mixing temperatures can vary depending on the particular formulation.
SteD 2 Ootionals - Aeration. Minor Addition~
and Flash DrYinq ODtionals Aerate (optional) said mix and add perfume (only if drying) and other minors with positive displacement pump or other in-line mixer. Example 28 is not aerated or dried. The mixture of Step (1) is optionally dried to reduce the amount of said water to the desired level, preferably 20-40% water. The flash drying tem-perature is from about 225-F to about 315-F (135~-157-C~ at pressure of from about 30 to abut 100 psi (115-517 mm Hg).
SteD 3 - Freezer Cool the mix using a scraped wall heat exchanger (freezer) to partially crystallize the components from an initial temperature of from about 180-F to about 200-F (82--93-C) or from about 200~F
to about 22~-F (93--104-C), if dried, to a final temperature preferably from about 135-F to about 180-F (57--82-C), more preferably from about 145-F to about 180-F (63--82-C), and most preferably from about 155-F to about 175~F (68 -79 C). This final temperature, also referred to herein as the Freezer Outlet Temperature (FOT), is typically the maximum temperature that will form a smooth plug that holds its shape once extruded onto a moving belt (Step 4). The FOT for Example 28 is 175-F.
SteD 4 - Extrusion The cooled mix of Step 3 is extruded out onto a moving belt as a soft plug which is then cooled and fully crystallized and then stamped and packaged. The plugs are preferably formed via an extrusion operation, as shown in U.S. Pat. No. 3,835,059, supra Some of the composition crystallizes in the freezer (Step 3) in order to provide a semi-solid having a sufficient viscosity to stand up on the belt, while further crystallization occurs after 3~ extrusion, resulting in hardening of the bar. The final crystal-lization of the sodium soap forms the interlocking, semi-con-tinuous, open mesh structure in the freezer bar of the present 20Y~3~1 WO 92/09679 PCr/US9 1 /08733 invention.
Inqredient Wt.%
Sodium C14 Soap 27.99 Magnesium C14 Soap 5.00 Sodium Lauroyl Sarcosinate 3.00 Coco Betaine 10.00 Propylene Glycol 3.50 Petrolatum 22. 49 Sodium Chloride 2.58 Free ~atty Acid, C14 0.50 Perfume 0.50 Water 24. 44 The Plodding StamPed Bar Hardness Test The Plodding Stamped Bar Hardness Test can be used to differentiate the bars of this invention from other bars. Four trade bars are selected that represent various soap processes:
SAFEGUARD9, a soap milled bar; ZEST~, a soap/synthetic milled bar;
IVORY0, a freezer bar; and LAVA~, a framed bar. Samples of these market bars and formed bars of Example 28 and Example II are plodded using the procedure set out below.
Overall, the market bars after plodding are much harder and have a better smear versus Example 28 or Example II after plod-ding. This data is detailed in Table 12. This test clearly is an excellent method of differentiating bars containing the rigid skeletal structure versus other bars. Simply stated, the bars of this invention will become much more soft after replodding than conventional bars.
The procedure is as follows:
1. Formed bars (about 2.5 Kg or greater) are placed into a single stage plodder (4 inch/10.16 cm bonnet single stage plodder) without vacuum and are run through a noodle plate.
The noodle plate contains nineteen 0.37 inch (0.93 cm) holes in a 3.1 inch (8 cm) plate. The barrel temperature is set at 120-F (49~C) and the nose temperature is set at 110~F
(43.5~C)-2. Step 1 is repeated with the noodles.
W O 92/09679 2 0 9 5 3 5 1 '' ~ - PC~r/US91/08733 3. The noodles of Step 2 are placed into the single stage plodder (4 inch/10.16 cm bonnet single stage plodder) with vacuum applied and run through a brick-shaped orifice. A
brick-shaped plug with approximate dimensions of 1.88 inches (4.6 cm) (height) by 1.16 inches (3 cm) (width) by 3 inches (7.6 cm) (length) is extruded. These plugs should have an interior temperature of 90'F (32~C) to 105-F (41-C).
4. These plugs are stamped into a brick shape and are allowed to cool to room temperature (at least 12 hours) before evalua-tion. TABLE 12 Bar Plodder Data Bar Hardness (mm~*
1 SAFEGUARD~ Market Bar 3.18 2 SAFEGUARD~ (Plodded/Stamped) 3.13 Delta (The value of Bar 1-Bar 2) 0.05 1 ZEST~ Market Bar 2.25 2 ZEST~ (Plodded/Stamped) 2.33 Delta (0.08) 1 IVORY~ Market Bar 1.g3 2 IVORY~ (Plodded/Stamped) 3.03 Delta (1.10) 1 LAVA~ Market Bar 1.90 2 LAVA~ (Plodded/Stamped) 2.47 Delta (0.57) 1 Example 28 (Formed Bar) 3.35 2 Example 28 (Plodded/Stamped) 10.67 Delta (7.32) 1 Example II (Formed Bar) 6.43 2 Example II (Plodded/Unstamped)18.07 Delta (11.64) *The "hardness" of the "plodder/stamped" bars is reported as Bar 2 in Table 12 for each bar tested. The Bar Hardness Test is set out herein elsewhere.
20g j~,3 jl ~~O 92/09679 PCI/US91/08733 - 42 -While not being bound to a theory, plodded bars with Delta'sof 4 or greater is a strong indication that there is a skeletal structure in the original which is fractured or destroyed when plodded. The hard bars of the present invention will form soft, messy bars when plodded in a conventional bar process.
The bars of Example 28 bars are first formed using the above freezer process. The bars of Example II are first formed using the above-described frame bar process.
About 5-10 Kg of each bar is plodded and stamped.
The market bars are made of tallow and coconut natural soaps.
The hardness of plodded SAFEGUARD9 and ZEST~ bars are about the same as the original bars. The IVORY~ and LAVA~ plodded bars (2) are slightly softer than the original bars.
On the other hand, the plodded Bar 2 of Example 28 is much softer than the original Bar 1 of Example 28. More dramatically, the plodded Bar 2 of Example II falls apart upon plodding and is too soft to stamp. Its hardness after plodding is that of a soft aqueous phase, indicating that the rigidity of the skeletal structure is essentially destroyed.
WHAT IS CLAIMED IS:
Some bars of this invention comprise: more than 5% to 50%
fibrous sodium fatty acid soap composed of at least about 50%
saturated fatty alkyl chains having 12-24 carbon atoms of which at least about 25% of said saturated fatty alkyl chains is of a 15 S i ngle chain length.
Some bars of this invention comprise said fibers which occupy from about 3% to about 75%, preferably from about 15% to about 40%, of the volume of the bar structure.
Some bars comprise a rigid, low smearing structure of: more 20 than 5% to 75% sodium fatty acid soap composed of at least about 50% saturated fatty alkyl chains having 12-24 carbon atoms of which at least about 25% of said saturated fatty alkyl chains is of a single chain length; from about 10% to about 94% water; and about 0% to a total of about 70% of other selected soap bar 25 ingredients selected from the group set out above in Table 4.
Some personal cleansing soap bar compositions comprise a rigid interlocked mesh of sodium soap fibers; wherein the sodium fatty acid soap is composed of at least about 50% saturated fatty alkyl chains having 12-24 carbon atoms of which at least about 25%
of said saturated fatty alkyl chains is of a single chain length;
and from about 2% to about 40% by weight of a hygroscopic synthet-ic surfactant wherein said hygroscopic synthetic surfactant is selected from surfactants which absorb at least about 20% of its dry weight in water at 26~C and 80% Relative Humidity in three '5 days.
W O 92/09679 2 0 9 S 3 5 1 PC~r/US91/08733 Bar ADDearance Aids Bar appearance (water-retaining and/or shrinkage prevention) aids are preferably selected from the group consisting of:
compatible salt and salt hydrates;
water-soluble organics such as polyols, urea;
aluminumosilicates and clays; and mixtures thereof, as set out above in Table 4.
Water-soluble organics are also used to stabilize the appear-ance of the bar soaps of the present invention. Some preferred water-soluble organics are propylene glycol, glycerine, ethylene glycol, sucrose, and urea, and other compatible polyols.
A particularly suitable water-soluble organic is propylene glycol. Other compatible organics include polyols, such as ethylene glycol or 1,7-heptane-diol, respectively the mono- and polyethylene and propylene glycols of up to about 8,000 molecular weight, any mono-Cl 4 alkyl ethers thereof, sorbitol, glycerol, glycose, diglycerol, sucrose, lactose, dextrose, 2-pentanol, l-butanol, mono- di- and triethanolammonium, 2-amino-1-butanol, and the like, especially the polyhydric alcohols.
The term "polyol" as used herein includes non-reducing sugar, e.g., sucrose. Sucrose will not reduce Fehling's solution and therefore is classified as a "non-reducing" disaccharide. Unless otherwise specified, the term "sucrose" as used herein includes sucrose, its derivatives, and similar non-reducing sugars and similar polyols which are substantially stable at a soap pro-cessing temperature of up to about 210-F (98-C), e.g., trialose, raffinose, and stachyose; and sorbitol, lactitol and maltitol.
Compatible salt and salt hydrates are used to stabilize the bar soap appearance via the retention of water. Some preferred salts are sodium chloride, sodium sulfate, disodium hydrogen phosphate, sodium pyrophosphate, sodium tetraborate.
Generally, compatible salts and salt hydrates include the sodium, potassium, magnesium, calcium, aluminum, lithium, and ammonium salts of inorganic acids and small (6 carbons or less) carboxylic or other organic acids, corresponding hydrates. and mixtures thereof, are applicable. The inorganic salts include chloride, bromide, sulfate, metasilicate, orthophosphate, pyro-phosphate, polyphosphate, metaborate, tetraborate, and carbonate. The organic salts include acetate, formate, methyl sulfate, and citrate.
Water-soluble amine salts can also be used. Monoethanolamine, diethanolamine, and triethanolammonium (TEA) chloride salts are preferred.
5Aluminosilicates and other clays are useful in the present invention.
Some preferred clays are disclosed in U.S. Pat. Nos. 4,605,509 and 4,274,975.
Other types of clays include zeolite, kaolinite, montmorillonite, attapulgite, illite, bentonite, and halloysite. Another preferred clay is kaolin.
10Waxes include petroleum based waxes (paraffin, microcrystalline, and petrolatum), vegetable based waxes (carnauba, palm wax, candelilla, sugarcane wax, and vegetable derived triglycerides) animal waxes (beeswax, spemaceti, wool wax, shellac wax, and animal derived triglycerides). mineral waxes (montar, ozokerite, and ceresin) and synthetic waxes (Fischer-Tropsch).
15A preferred wax is used in the Examples herein. A useful wax has a melting point (M.P.) of from about 120~F to about 185~F (49-85~C), preferably from about 125~F to about 175~F (52~-79~C). A preferred paraffin wax is a fully refined petroleum wax having a melting point ranging from about 130~F
to about 140~F (49~-60~C). This wax is odorless and tasteless and meets FDA
requirements for use as coatings for food and food packages. Such paraffins are readily available commercially. A very suitable paraffin can be obtained, for example, from The Standard Oil Company of Ohio under the trade mark Factowax R-133.
Other suitable waxes are sold by the National Wax Co. under the trade 25names of 9182 and 6971, respectively, having melting points of 131~F and 130~F(-55~C).
The paraffin preferably is present in the bar in an amount ranging from about 5X to about 20% by weight. The paraffin ingredient is used in the product to impart skin mildness, plasticity, firmness, and processability.
It also provides a glossy look and smooth feel to the bar.
The paraffin ingredient is optionally supplemented by a microcrystalline wax. A suitable microcrystalline wax has a melting point ranging, for example, from about 140-F (60-C) to about 185-F (85-C), preferably from about 145'F (62-C) to about 175-F (79-C). The wax preferably should meet the FDA requirements for food grade microcrystalline waxes. A very suitable micro-crystalline wax is obtained from Witco Chemical Company under the trade mark Multiwax X-145A. The microcrystalline wax preferabiy is present in the bar in an amount ranging from about 0.5% to about 5% by weight. The microcrystalline wax ingredient imparts pliability to the bar at room temperatures.
EXAMPLES
The following examples are illustrative and are not intended to limit the scope of the invention. Unneutralized or "free"
fatty acids, as used in the examples, are of the same chain lengths as those used to make the soaps, unless otherwise speci-fied. All levels and ranges, temperatures, results, etc., used herein, are approximations unless otherwise specified.
A Frame Process for Makinq the Bars of the Present Invention The cleansing bars in the Examples are made by the following procedure unless otherwise specified:
1. Fatty acid precursor, propylene glycol, sodium chloride, and water (excluding water coming in with other raw materials) are mixed and heated to 71'C.
2. Caustic solution (50% sodium hydroxide) is added and the mixture is stirred until smooth forming an aqueous molten liquid comprising from 15% to 94% water and from 5.5% to 75% soap (neutralized carboxylic acid). The temperature during neutralization of the molten liquid increases to -95-C.
3. Other ingredients are added preferably in the following order and the temperature is maintained at -88-C: coco betaine; sodium lauroyl sarcosinate; or sodium alpha-sulfo methyl cocoate; kaolin clay; or hydrated zeolite (synthetic sodium aluminosilicate); and paraffin.
Perfume is added last.
4. The molten liquid mixture is poured into shaped molds.
W O 92/09679 2 0 9 ~3 51 - 30 - P~/US91/08733 5. The molten liquid crystallizes (solidifies) on cooling to room temperature and the resultant bars are removed from the molds.
The bars of the examples are made using the above general procedure, unless otherwise specified.
It is important to note that, when the formulations which are used in the Examples of the present invention are subjected to a conventional plodding or freezer process very soft or no bars are formed. Example II is a very highly preferred overall bar.
Preferred Bars Ex. I Ex. IIEx. III Ex. IV
Ingredient (Wt.%) (Wt.%)(Wt.%) (Wt.~,') Na C14 Soap 20 20 - -Na C16 Soap - - 20 16 K C16 Soap - - - 4 Free Fatty Acid Sodium Lauroyl Sarcosinate 7 7 12 Sodium Alpha Sulfo Methyl Cocoate - - - 7 Coco Betaine 5 5 7 5 Sodium Chloride 3.0 3.0 3.0 3.0 Propylene Glycol 14.5 14.5 14.5 15.0 Hydrated Zeolite A
(Aluminosilicate) 4.0 4.0 Kaolin Clay 4.0 - 4.0 Paraffin (M.P.=55-C) 6.5 6.5 4.5 Perfume Water 37.25 37.25 31.95 36.25 Hardness (mm~ 5.5 6.4 4.2 5.1 Smear 9.5 9.0 8.5 8.5 ~escription of Testinq for ExamPles 35Bar Hardness Test 1. The hardness of a bar is determined by measuring at 25~C
the depth of penetration (in mm) into the bar of a 247 gram , ~ ~
; .
Standard Weighted Penetrometer Probe having a conically shaped needle attached to a 22.9 cm (9 inch) shaft weighing 47 grams with 200 grams on top of said shaft. A hardness measurement of 5 mm or less indicates a very hard bar; 5-10 mm indicates a moderately hard bar; 10-12 mm indicates a somewhat soft bar of marginal acceptance; and greater than 12 mm indicates a very soft bar that is unacceptable for most uses. This defines "hardness" as used herein unless otherwise specified.
Bar Smear Test 2. The smear grade is determined by a (1) placing a soap bar on a perch in a 1400 mm diameter circular dish; (2) adding 200 ml of room temperature water to the dish such that the bottom 3 mm of the bar is submerged in water; (3) letting the bar soak over-night (15 hours); (4) turn the bar over and grade qualitatively for the combined amount of smear, and characteristics of smear, depth of smear on a scale where 10 equals no smear, 8.0-9.5 equals low smear amount, 5.0-7.5 equals moderate smears similar to most marketed bars, and 4.5 or less equals very poor smear.
Commercial soap bars, e.g., SAFEGUARD~, ZEST~, IVORY~, and LAVA~, have smears of about 5, 6, 6, and 6, respectively. See Table 12 for more data.
Bar Shrinkaqe Test 3. Shrinkage is measured by placing a freshly made un-wrapped bar in a room that is held at 26~C and 15% relative humidity for one week. The amount of shrinkage from the original bar shape is determined on a qualitative scale where O indicates no shrinkage, + indicates slight shrinkage, ++ indicates moderate shrinkage, and +++ indicates great shrinkage.
In Tables 6 and 7, soap bars 1-10 are set out to show bar hardness, smear and shrinkage for C1o, Cl2~ C14, C16~ and C18 alkyl chain soaps as shown. The preferred alkyl chain soaps of the present invention are set out above in Tables l and 2.
The term "X." means that the example is a comparative example.
WO 92/09679 2 0 9 S3~1 32 PCI/US91/08733 Sinqle Saturated Chain Lenqth Sodium Soap/Water StudY
Ex.1 Ex.2 Ex.3 Ex.4 Ex.5 Ingredient Wt.% Wt.% Wt.% Wt.% Wt.%
Sodium Soap Free Fatty Acid 1.0 1.0 1.0 1.0 2.0 Excess Sodium Hydroxide Sodium Chloride 2.0 1.0 1.0 1.0 1.0 Water 64 65 65 65 64 Hardness (mm) 8.9 2.3 2.2 5.4 4.2 Smear 3 10 10 9.5 10.0 Shrinkage +++ +++ + 0 Note that Ex. 1 has a very poor smear, notwithstanding a hardness of 8.9 as the smear methodology dissolves away the soluble C1o soap.
Single Chain Lenqth Sodium SoaD/Water StudY
X.6 Ex.7 Ex.8 Ex.9 Ex.10 Ingredient Wt.% Wt.% Wt.% Wt.% Wt.~o Sodium Soap C18:1 33 Free Fatty Acid 1.0 - 2.0 1.0 Excess Sodium Hydroxide - 0.07 Sodium Chloride 1.0 1.0 1.0 1.0 1.0 Water 65 87 82.8 83 94 W O 92/09679 2 0 9 S 3 S 1 ' - P ~ /US91/08733 _ - 33 -Hardness (mm) ** 11.8 11.9 14.0 Smear 10.0 10.0 9.0 Shrinkage 0 +++ ++++ ++++
** Solid bar not formed due to too much unsaturated soap.
Example 10 has the rigid structure, but is not preferred as a cleaning bar because its hardness is 14.
BinarY Chain Lenqth Sodium SoaD/Water Study X.11 Ex.12 Ex.13 InqredientWt.% Wt.% Wt.%
Sodium Soap C10 - - 16.5 Cl2 16.5 - -C14 - 16.5 16.5 C1g:1 16.5 16.5 Free Fatty Acid 1.0 1.0 1.0 Excess Sodium Hydroxide Sodium Chloride 1.0 1.0 1.0 Water 65 65 65 Hardness (mm) ** 9.0 9.0 Smear 9.0 8.0 **Solid Bar not formed due to too much unsaturation combined with C12 soap.
W O 92/09679209 ~ 3Sl ~ P~/US91/08733 Binarv Saturated Chain Lenqth Sodium SoaD/Water Studv Ex.14 Ex.15 Ex.16 Inqredient Wt.% Wt.% Wt.%
Sodium Soap Cl2 16.5 C14 16.5 C16 - 16.5 10 C18 - 16.5 10 Free Fatty Acid 1.0 1.0 1.0 Sodium Chloride 1.0 1.0 1.0 Water 65 65 78 Hardness (mm) 2.8 4.5 7.3 Smear 9.5 10.0 10.0 Shrinkage 0 ++
Examples 12-16 are excellent bars of the present invention.
20ComDlex Chain Lenqth Sodium SoaD/Water Studv Ex.17 Ex.18 Ex.19 Inqredient Wt.% Wt.% Wt.%
Sodium Soap*
Emersol 132 - (33) (15) C8 0.56 C1o 0.64 Cl2 10.14 0.12 8.1 (8.0) C14 4.54 0.79 10.4 (10.0) C16 8.51 15.6 7.10 C17 0.76 0.76 0.35 Cl8 19.85 15.3 7.0 C20 - 0.26 0.12 Free Fatty Acid - 1.0 Sodium Chloride 1.1 1.0 1.0 Water 53.9 65 66 W O 92/09679 2 0 9 5 3 5 1 P ~ /US9l/08733 Hardness (mm) 7.6 4.7 5.8 Smear 9.5 10 9.5 Shrinkage + ++
*Composition by Chain Length, () indicate actual level of materials.
Examples 17-19 are made with more complex mixtures of soaps than the prior examples. They form very good bars of the present invention. They have little or no smear. Compare their hardness and smears with those made with conventional tallow and coconut soap shown in Table 11 .
ComPlex Chain Lenqth Sodium SoaD/Water StudY
X.20 X.21 X.22 Inqredient Wt.% Wt.% Wt.%
Sodium Soap*
Tallow (33) - (26.4) Coconut - (33) (6.6) C8 - 2.31 0.46 C10 - 2.0 0.40 C12 ~ 16.5 3.3 C14 1.0 5.94 4.95 Cl6 7.92 2.81 6.90 C18 0-5 - 0.40 C20 6.6 1.0 5.48 C14:1 0.33 - 0.26 C16:1 0.83 - 0.66 C1g:1 14.2 2.0 11.76 C1g:2 0.75 0.5 0-7 Free Fatty Acid 1.0 1.0 1.0 Sodium Chloride 1.0 1.0 1.0 Water 65 65 65 Hardness (mm) Soft 15.8 12.5 ~5 Smear Poor 3.0 5.0 *Composition by Chain Length, () indicate actual level of materials.
W O 92/09679 2 0 9 5 ~ S I 36 P~/US91/08733 These comparative examples, X.20, X.21, and X.22, do not form the rigid structure of the present invention. Note that they are made with the typical commercial soaps. They are soft soaps with terrible smears. Compare with Example 15 of the present invention ; which is made with 65% water and C16 and C1g saturated soap and forms a hard bar with no smear.
Example 23 is a bar of the present invention which contains more synthetic surfactant than soap. It has low smear and good lather. Example 24 is a bar of the present invention which contains polymer and other bar soap ingredients.
SYndet Bar ExamPle Inqredient Wt.%
Sodium Palmitate 20 Sodium Lauroyl Sarcosinate 9*
Sodium Laureth-3 Sulfate 7*
Sodium Cetearyl Sulfate 5*
Free Fatty Acid (Palmitic) Sodium Chloride 3 Propylene Glycol 14 Hydrated Zeolite A 3 Perfume Water 37 *Total 21% Synthetic Surfactant 20953~1 WO 92/09679 i P~/US91/08733 PolYmer-Containinq ExamDle Ingredient Wt.%
Sodium Palmitate 20 Sodium Alpha-Sulfo Methyl Cocoate 8. 7 Coco Betaine 4.65 Jaguar C376 1.5 Propylene Glycol 15 Kaolin Clay 5 Paraffin, (M.P.=55-C) 4.5 Sodium Chloride 3 Perfume Water 35.5 Examples 23 and 24 are similar to Example IV of Table 5.
Example 24 is a mild bar formulation with polymeric skin mildness aid.
Ex. 25 Ex. 26 Ex.27 Inqredient Wt.% Wt.% Wt.%
Lithium Myristate 33 Lithium Chloride 5 - -Disodium Salt of Dodecanedioic Acid - 20 20 Sodium Lauroyl Sarcosinate - - 5 Water 62 80 75 Penetration Values N/A N/A N/A
N/A = Not available For Example 25, the formulation is prepared by heating the fatty acid precursor to 71-C, separately adding lithium hydroxide to water, and then adding the fatty acid and lithium hydroxide solution together, mixing together for 30 minutes maintaining the 35 heat at least at 71-C, adding lithium chloride salt and stirring for an additional 5 minutes, then pouring into a mold and letting ...
.. ~ . D
",, f ' cool and solidify. A solid bar with excellent smear properties is formed.
For Examples 26 and 27, the diacid is melted (150-180~C) and a hot (90~C) caustic solution (two equivalents of NaOH) is added. The mixture is stirred for -5 minutes. For Example 27, the sodium lauroyl sarcosinate is predissolved in the caustic/water solution. The bar becomes solid on cooling, with further hardening occurring upon degradation, e.g., to about 35-40% water by weight of the bar.
Example 25 demonstrates the ability to form high moisture, firm and non-smearing bars without the need for sodium soap. Examples 26 and 27 demonstrate the ability to form a totally soap-free product and still obtain the relatively rigid intermeshed fiber structure.
Example 28 below is made by a freezer bar process disclosed in commonly assigned, Canadian Pat. Application Ser. No. 2,113,564, Taneri et al. This process provides a personal cleansing freezer bar comprising a skeleton structure having a relatively rigid, interlocking, semi-continuous, open, three-dimensional, crystalline mesh of neutralized carboxylic acid soap made by the following steps:
(1) mixing a molten mixture comprising by weight of said bar:
20from about 15% to about 85% of said soap and from about 15%
to about 40% water;
(2) cooling said mixture to a semi-solid in a scraped wall heat exchanger freezer;
(3) extruding said semi-solid as a soft plug; and 25(4) further cooling and crystallizing said soft plug until firm to provide said personal cleansing freezer bar.
Step 1 - Mixinq The soap specified in the formulation is made in situ by mixing the desired fatty acids, consisting essentially of C12-C24 chain lengths, with the appropriate base or mixture of bases, consisting essentially of sodium, lithium, magnesium, calcium, and potassium hydroxide and triethanolamine. The fatty acid, base, and water are mixed at from about 170~F to about 200~F (76~-93~) 209~3~1 WO 92/09679 PCI'/US91/08733 - 3g -to form the soap. In Example 28, 180-F is used. Sufficient water is used such that the mixture is stirrable. The other ingredients are added, maintaining the temperature of from about 180-F to about 200-F (82--93-C). Example 28 - 180-F. The optimal mixing temperatures can vary depending on the particular formulation.
SteD 2 Ootionals - Aeration. Minor Addition~
and Flash DrYinq ODtionals Aerate (optional) said mix and add perfume (only if drying) and other minors with positive displacement pump or other in-line mixer. Example 28 is not aerated or dried. The mixture of Step (1) is optionally dried to reduce the amount of said water to the desired level, preferably 20-40% water. The flash drying tem-perature is from about 225-F to about 315-F (135~-157-C~ at pressure of from about 30 to abut 100 psi (115-517 mm Hg).
SteD 3 - Freezer Cool the mix using a scraped wall heat exchanger (freezer) to partially crystallize the components from an initial temperature of from about 180-F to about 200-F (82--93-C) or from about 200~F
to about 22~-F (93--104-C), if dried, to a final temperature preferably from about 135-F to about 180-F (57--82-C), more preferably from about 145-F to about 180-F (63--82-C), and most preferably from about 155-F to about 175~F (68 -79 C). This final temperature, also referred to herein as the Freezer Outlet Temperature (FOT), is typically the maximum temperature that will form a smooth plug that holds its shape once extruded onto a moving belt (Step 4). The FOT for Example 28 is 175-F.
SteD 4 - Extrusion The cooled mix of Step 3 is extruded out onto a moving belt as a soft plug which is then cooled and fully crystallized and then stamped and packaged. The plugs are preferably formed via an extrusion operation, as shown in U.S. Pat. No. 3,835,059, supra Some of the composition crystallizes in the freezer (Step 3) in order to provide a semi-solid having a sufficient viscosity to stand up on the belt, while further crystallization occurs after 3~ extrusion, resulting in hardening of the bar. The final crystal-lization of the sodium soap forms the interlocking, semi-con-tinuous, open mesh structure in the freezer bar of the present 20Y~3~1 WO 92/09679 PCr/US9 1 /08733 invention.
Inqredient Wt.%
Sodium C14 Soap 27.99 Magnesium C14 Soap 5.00 Sodium Lauroyl Sarcosinate 3.00 Coco Betaine 10.00 Propylene Glycol 3.50 Petrolatum 22. 49 Sodium Chloride 2.58 Free ~atty Acid, C14 0.50 Perfume 0.50 Water 24. 44 The Plodding StamPed Bar Hardness Test The Plodding Stamped Bar Hardness Test can be used to differentiate the bars of this invention from other bars. Four trade bars are selected that represent various soap processes:
SAFEGUARD9, a soap milled bar; ZEST~, a soap/synthetic milled bar;
IVORY0, a freezer bar; and LAVA~, a framed bar. Samples of these market bars and formed bars of Example 28 and Example II are plodded using the procedure set out below.
Overall, the market bars after plodding are much harder and have a better smear versus Example 28 or Example II after plod-ding. This data is detailed in Table 12. This test clearly is an excellent method of differentiating bars containing the rigid skeletal structure versus other bars. Simply stated, the bars of this invention will become much more soft after replodding than conventional bars.
The procedure is as follows:
1. Formed bars (about 2.5 Kg or greater) are placed into a single stage plodder (4 inch/10.16 cm bonnet single stage plodder) without vacuum and are run through a noodle plate.
The noodle plate contains nineteen 0.37 inch (0.93 cm) holes in a 3.1 inch (8 cm) plate. The barrel temperature is set at 120-F (49~C) and the nose temperature is set at 110~F
(43.5~C)-2. Step 1 is repeated with the noodles.
W O 92/09679 2 0 9 5 3 5 1 '' ~ - PC~r/US91/08733 3. The noodles of Step 2 are placed into the single stage plodder (4 inch/10.16 cm bonnet single stage plodder) with vacuum applied and run through a brick-shaped orifice. A
brick-shaped plug with approximate dimensions of 1.88 inches (4.6 cm) (height) by 1.16 inches (3 cm) (width) by 3 inches (7.6 cm) (length) is extruded. These plugs should have an interior temperature of 90'F (32~C) to 105-F (41-C).
4. These plugs are stamped into a brick shape and are allowed to cool to room temperature (at least 12 hours) before evalua-tion. TABLE 12 Bar Plodder Data Bar Hardness (mm~*
1 SAFEGUARD~ Market Bar 3.18 2 SAFEGUARD~ (Plodded/Stamped) 3.13 Delta (The value of Bar 1-Bar 2) 0.05 1 ZEST~ Market Bar 2.25 2 ZEST~ (Plodded/Stamped) 2.33 Delta (0.08) 1 IVORY~ Market Bar 1.g3 2 IVORY~ (Plodded/Stamped) 3.03 Delta (1.10) 1 LAVA~ Market Bar 1.90 2 LAVA~ (Plodded/Stamped) 2.47 Delta (0.57) 1 Example 28 (Formed Bar) 3.35 2 Example 28 (Plodded/Stamped) 10.67 Delta (7.32) 1 Example II (Formed Bar) 6.43 2 Example II (Plodded/Unstamped)18.07 Delta (11.64) *The "hardness" of the "plodder/stamped" bars is reported as Bar 2 in Table 12 for each bar tested. The Bar Hardness Test is set out herein elsewhere.
20g j~,3 jl ~~O 92/09679 PCI/US91/08733 - 42 -While not being bound to a theory, plodded bars with Delta'sof 4 or greater is a strong indication that there is a skeletal structure in the original which is fractured or destroyed when plodded. The hard bars of the present invention will form soft, messy bars when plodded in a conventional bar process.
The bars of Example 28 bars are first formed using the above freezer process. The bars of Example II are first formed using the above-described frame bar process.
About 5-10 Kg of each bar is plodded and stamped.
The market bars are made of tallow and coconut natural soaps.
The hardness of plodded SAFEGUARD9 and ZEST~ bars are about the same as the original bars. The IVORY~ and LAVA~ plodded bars (2) are slightly softer than the original bars.
On the other hand, the plodded Bar 2 of Example 28 is much softer than the original Bar 1 of Example 28. More dramatically, the plodded Bar 2 of Example II falls apart upon plodding and is too soft to stamp. Its hardness after plodding is that of a soft aqueous phase, indicating that the rigidity of the skeletal structure is essentially destroyed.
WHAT IS CLAIMED IS:
Claims (20)
1. A personal cleansing bar composition comprising a rigid, crystalline interlocking mesh of elongated sodium soap crystals; said soap bar comprising:
from about 15% to about 50% sodium fatty acid soap composed of at least about 50% saturated fatty alkyl chains having 12-24 carbon atoms of which at least about 25% of said saturated fatty alkyl chains is of a single chain length;
from about 15% to about 60% water; and from about 2% to about 60% by weight of a hygroscopic synthetic surfactant wherein said hygroscopic synthetic surfactant is selected from surfactants which absorb at least about 20% of their dry weight in water at 26°C and 80% Relative Humidity in three days.
from about 15% to about 50% sodium fatty acid soap composed of at least about 50% saturated fatty alkyl chains having 12-24 carbon atoms of which at least about 25% of said saturated fatty alkyl chains is of a single chain length;
from about 15% to about 60% water; and from about 2% to about 60% by weight of a hygroscopic synthetic surfactant wherein said hygroscopic synthetic surfactant is selected from surfactants which absorb at least about 20% of their dry weight in water at 26°C and 80% Relative Humidity in three days.
2. A cleansing bar composition comprising at least two phases;
an aqueous phase having a penetration value of 12 mm for a 12 mm deep sample, said aqueous phase being soft or flowable at 25°C;
a rigid crystalline phase skeleton structure comprising an interlocking, open three-dimensional mesh of neutralized mono- and/or di-carboxylic acid elongated crystals;
wherein said cleansing bar comprising said rigid crystalline phase skeleton structure and said aqueous phase has a penetration value of from zero to about 12 mm for a 25 mm deep sample of said cleansing bar;
wherein said penetration values are measured as 25°C, using a 247 gram Standard Weighted Penetrometer Probe having a conical needle attached to a 9 inch (22.9 cm) shaft, weighing 47 grams with 200 grams on top of said shaft for a total of said 247 grams, said conical needle having a 19/32 inch (1.51 cm) top and a 1/32 inch (0.08 cm) point; and wherein said neutralized carboxylic acid is selected from the group consisting of lithium and/or sodium neutralized; monocarboxylic acid and/or dicarboxylic acid; and mixtures thereof;
wherein said monocarboxylic acid has a fatty alkyl chain of from about 12 to about 24 carbon atoms;
wherein at least about 80% of said carboxylic acid has saturated alkyl chains;
wherein said rigid crystalline phase skeleton structure occupies from about 3% to about 75% of said cleansing bar by volume; and wherein said neutralized carboxylic acid comprises from over 5% to about 75% by weight of said cleansing bar; and wherein said cleansing bar contains from about 15% to about 94% water.
an aqueous phase having a penetration value of 12 mm for a 12 mm deep sample, said aqueous phase being soft or flowable at 25°C;
a rigid crystalline phase skeleton structure comprising an interlocking, open three-dimensional mesh of neutralized mono- and/or di-carboxylic acid elongated crystals;
wherein said cleansing bar comprising said rigid crystalline phase skeleton structure and said aqueous phase has a penetration value of from zero to about 12 mm for a 25 mm deep sample of said cleansing bar;
wherein said penetration values are measured as 25°C, using a 247 gram Standard Weighted Penetrometer Probe having a conical needle attached to a 9 inch (22.9 cm) shaft, weighing 47 grams with 200 grams on top of said shaft for a total of said 247 grams, said conical needle having a 19/32 inch (1.51 cm) top and a 1/32 inch (0.08 cm) point; and wherein said neutralized carboxylic acid is selected from the group consisting of lithium and/or sodium neutralized; monocarboxylic acid and/or dicarboxylic acid; and mixtures thereof;
wherein said monocarboxylic acid has a fatty alkyl chain of from about 12 to about 24 carbon atoms;
wherein at least about 80% of said carboxylic acid has saturated alkyl chains;
wherein said rigid crystalline phase skeleton structure occupies from about 3% to about 75% of said cleansing bar by volume; and wherein said neutralized carboxylic acid comprises from over 5% to about 75% by weight of said cleansing bar; and wherein said cleansing bar contains from about 15% to about 94% water.
3. The personal cleansing bar composition of claim 1 wherein said hygroscopic synthetic surfactant is selected from the group consisting of alpha sulfo fatty acid esters; alkyl sulfates; alkyl ether carboxylates; alkyl betaines; alkyl sultaines; alkyl amine oxides; alkyl ether sulfates; and mixtures thereof.
4. The cleansing bar of claim 2 wherein at least 80% of said carboxylic acid has the following general formula:
wherein:
a + b = 8 to 20 each a, b = 0 to 20 X = H, OR,O-C-R, R, or mixtures thereof R = C1-C3 alkyl, H, or mixtures thereof M = Na, Li, or mixtures thereof.
wherein:
a + b = 8 to 20 each a, b = 0 to 20 X = H, OR,O-C-R, R, or mixtures thereof R = C1-C3 alkyl, H, or mixtures thereof M = Na, Li, or mixtures thereof.
5. The cleansing bar of claim 4 wherein said a + b = 10-16; each of said a, b = 0-16; said X = H, OR; R = H; and M = Na.
6. The cleansing bar of claim 2 wherein said elongated crystals are composed of fiber-like sodium fatty acid soap of which at least about 25% of said saturated fatty alkyl chains is of a single chain length; and wherein said bar contains: from about 15% to about 75% of said sodium soap; wherein said bar contains unneutralized (free) carboxylic acid of no more than 50% by weight of said soap.
7. The cleansing bar of claim 6 wherein said bar contains said sodium soap and water; and from about 2% to about 60% of a synthetic surfactant selected from the group consisting of: alkyl sulfates, paraffin sulfonates, alkylglycerylether sulfonates, acyl sarcosinates, methylacyl taurates, linear alkyl benzene sulfonates, N-acyl glutamates, alkyl glucosides, alpha sulfo fatty acid esters, acyl isethionates, alkyl sulfosuccinates, alkyl ether carboxylates, alkyl phosphate esters, ethoxylated alkyl phosphate esters, methyl glucose esters, protein condensates, alkyl amine oxides, alkyl betaines, alkyl sultaines, the alkyl ether sulfates with 1 to 12 ethoxy groups, and mixtures thereof, wherein said surfactants contain C8-C22 alkyl chains.
8. The cleansing bar of claim 7 wherein said synthetic surfactant is hygroscopic; said hygroscopic surfactant being defined as a surfactant which absorbs at least 20% of its dry weight in water at 26°C and 80% Relative Humidity in three days and wherein said bar is relatively non-swelling.
9. The cleansing bar of claim 8 wherein said hygroscopic surfactant is selected from the group consisting of alpha sulfo fatty acid esters; alkyl sulfates; alkyl ether carboxylates; alkyl betaines; alkyl sultaines; alkyl amine oxides; alkyl ether sulfates; and mixtures thereof.
10. The cleansing bar of claim 7 wherein the ratio of said water to said soap is from about 1:1 to about 5:1; said water is present at a level of from about 25% to about 60%; wherein said soap has fatty alkyl chains are C14 to C22 and said soap level in said bar is from about 15% to about 35%; wherein at least about 85% of said soap alkyl chains are saturated; wherein said unneutralized (free) carboxylic acid is from zero to about 25% by weight of said soap; and wherein said synthetic surfactant level is from about 4% to about 25% by weight of the bar and said surfactant is selected from the group consisting of: sodium acyl isethionates, sodium acyl sarcosinates, sodium alpha sulfo fatty acid esters, sodium paraffin sulfonates, sodium alkyl ether sulfates, sodium alkyl sulfates, sodium linear alkyl benzene sulfonates, alkyl betaines, alkyl sultaines, and trialkyl amine oxides.
11. The cleansing bar of claim 10 wherein the ratio of said water to soap ratio is from about 1.5:1 to about 2:1; said unneutralized (free) carboxylic acid is from zero to about 17% by weight of said soap; said water level is from about 30% to about 45%; said soap fatty alkyl chain is from about C14 to about C18; wherein at least about 95% of said alkyl chains are saturated; said soap level is from about 15% to about 30%; and said synthetic surfactant level is from about 8% to about 16%.
12. The cleansing bar of claim 7 wherein said bar contains from about 0.1%
to about 40% of a hydrophobic material selected from the group consisting of:
microcrystalline wax, petrolatum, carnauba wax, palm wax, candelilla wax, sugarcane wax, vegetable derived triglycerides, beeswax, spemaceti, lanolin, wood wax, shellac wax, animal derived triglycerides, montar, ozokerite, ceresin, and Fischer-Tropsch wax.
to about 40% of a hydrophobic material selected from the group consisting of:
microcrystalline wax, petrolatum, carnauba wax, palm wax, candelilla wax, sugarcane wax, vegetable derived triglycerides, beeswax, spemaceti, lanolin, wood wax, shellac wax, animal derived triglycerides, montar, ozokerite, ceresin, and Fischer-Tropsch wax.
13. The cleansing bar of claim 12 wherein said bar contains from about 2%
to about 35% of said hydrophobic material selected from the group consisting of petrolatum and wax, said petrolatum and wax, and mixtures thereof having a melting point of from about 49°C (120°F) to about 85°C (185°F).
to about 35% of said hydrophobic material selected from the group consisting of petrolatum and wax, said petrolatum and wax, and mixtures thereof having a melting point of from about 49°C (120°F) to about 85°C (185°F).
14. The cleansing bar of claim 13 wherein said bar comprises from about 5%
to about 25% by weight of the bar of paraffin wax.
to about 25% by weight of the bar of paraffin wax.
15. The cleansing bar of claim 7 wherein said bar contains from about 1%
to about 50% of a non-volatile, water-soluble, nonionic organic material having a solubility of at least 5 parts in 10 parts of water; and wherein said water-soluble nonionic organic material is selected from the group consisting of a polyol of the structure:
where R1 = H, C1 - C4 alkyl; R2 = H, CH3; and n = 1-200;
C2 - C10 alkane diols; sorbitol; glycerine; sugars; sugar derivatives; urea;
and ethanol amines of the general structure (HOCH2CH2)XNHy where x = 1-3;
y = 0-2; and x+y = 3, and mixtures thereof.
to about 50% of a non-volatile, water-soluble, nonionic organic material having a solubility of at least 5 parts in 10 parts of water; and wherein said water-soluble nonionic organic material is selected from the group consisting of a polyol of the structure:
where R1 = H, C1 - C4 alkyl; R2 = H, CH3; and n = 1-200;
C2 - C10 alkane diols; sorbitol; glycerine; sugars; sugar derivatives; urea;
and ethanol amines of the general structure (HOCH2CH2)XNHy where x = 1-3;
y = 0-2; and x+y = 3, and mixtures thereof.
16. The cleansing bar of claim 15 wherein said bar contains from about 2%
to about 40% of said non-volatile, water-soluble, nonionic organic material.
to about 40% of said non-volatile, water-soluble, nonionic organic material.
17. The cleansing bar of claim 16 wherein said non-volatile, water-soluble, nonionic organic material comprises from about 5% to about 20% by weight of the bar; and wherein said organic material is selected from the group consisting of: propylene glycol, glycerine, sucrose, and urea, and mixtures thereof.
18. The cleansing bar of claim 7 wherein said bar contains said sodium soap, said water, and said synthetic surfactant, and from about 0.1% to about 70% of other ingredients selected from the group consisting of:
from about 1% to about 10% said potassium soap;
from about 1% to about 35% said magnesium soap;
from about 1% to about 35% said calcium soap;
from about 1% to about 15% triethanolammonium soap;
from about 1% to about 60% of impalpable water-insoluble materials selected from the group consisting of calcium carbonate and talc;
from about 0.1% to about 20% of a polymeric skin feel aid;
from about 0.5% to about 25% of aluminosilicate clay and/or other clays; wherein said aluminosilicates and clays are selected from the group consisting of zeolites; kaolin, kaolinite, montmorillonite, attapulgite, illite, bentonite, halloysite, and calcined clays;
from about 1% to about 50% of salt and salt hydrates; and mixtures thereof; and wherein said salt and salt hydrate have a cation selected from the group consisting of: sodium, potassium, magnesium, calcium, aluminum, lithium, ammonium, monoethanol ammonium, diethanolammonium, and triethanolammonium; and wherein said salt and said hydrate have an anion selected from the group consisting of:
chloride, bromide, sulfate, metasilicate, orthophosphate, pyrophosphate, polyphosphate, metaborate, tetraborate, carbonate, bicarbonate, hydrogen phosphate, methyl sulfate, and mono- and polycarboxylate of 6 carbon atoms or less.
from about 1% to about 10% said potassium soap;
from about 1% to about 35% said magnesium soap;
from about 1% to about 35% said calcium soap;
from about 1% to about 15% triethanolammonium soap;
from about 1% to about 60% of impalpable water-insoluble materials selected from the group consisting of calcium carbonate and talc;
from about 0.1% to about 20% of a polymeric skin feel aid;
from about 0.5% to about 25% of aluminosilicate clay and/or other clays; wherein said aluminosilicates and clays are selected from the group consisting of zeolites; kaolin, kaolinite, montmorillonite, attapulgite, illite, bentonite, halloysite, and calcined clays;
from about 1% to about 50% of salt and salt hydrates; and mixtures thereof; and wherein said salt and salt hydrate have a cation selected from the group consisting of: sodium, potassium, magnesium, calcium, aluminum, lithium, ammonium, monoethanol ammonium, diethanolammonium, and triethanolammonium; and wherein said salt and said hydrate have an anion selected from the group consisting of:
chloride, bromide, sulfate, metasilicate, orthophosphate, pyrophosphate, polyphosphate, metaborate, tetraborate, carbonate, bicarbonate, hydrogen phosphate, methyl sulfate, and mono- and polycarboxylate of 6 carbon atoms or less.
19. The cleansing bar of claim 2 wherein said elongated crystals contain platelets and wherein said soap consists of lithium neutralized monocarboxylic acid.
20. The cleansing bar of claim 2 wherein said elongated crystals are fiber-like and wherein said neutralized dicarboxylic acid is the disodium salt 1,12-dodecanedioic acid and wherein said neutralized dicarboxylic acid comprisesfrom about 20% to about 70% by weight of said bar.
Applications Claiming Priority (4)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US61782790A | 1990-11-26 | 1990-11-26 | |
US617,827 | 1990-11-26 | ||
US07/782,956 US5340492A (en) | 1990-11-26 | 1991-11-01 | Shaped solid made with a rigid, interlocking mesh of neutralized carboxylic acid |
US782,956 | 1991-11-01 |
Publications (2)
Publication Number | Publication Date |
---|---|
CA2095351A1 CA2095351A1 (en) | 1992-05-27 |
CA2095351C true CA2095351C (en) | 1998-12-15 |
Family
ID=27088104
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
CA002095351A Expired - Fee Related CA2095351C (en) | 1990-11-26 | 1991-11-20 | Shaped solid made with a rigid, interlocking mesh of neutralized carboxylic acid |
Country Status (27)
Country | Link |
---|---|
EP (1) | EP0559837B1 (en) |
JP (1) | JPH06503122A (en) |
KR (1) | KR100226393B1 (en) |
CN (1) | CN1036529C (en) |
AR (1) | AR247426A1 (en) |
AT (1) | ATE129522T1 (en) |
AU (1) | AU657295B2 (en) |
BR (1) | BR9107125A (en) |
CA (1) | CA2095351C (en) |
CZ (1) | CZ283495B6 (en) |
DE (1) | DE69114143T2 (en) |
DK (1) | DK0559837T3 (en) |
EG (1) | EG19580A (en) |
ES (1) | ES2079180T3 (en) |
FI (1) | FI932366A0 (en) |
GR (1) | GR3017892T3 (en) |
HU (1) | HU215484B (en) |
IE (1) | IE72087B1 (en) |
MA (1) | MA22349A1 (en) |
MX (1) | MX9102229A (en) |
NO (1) | NO931848L (en) |
NZ (1) | NZ240709A (en) |
PT (1) | PT99606A (en) |
RU (1) | RU2080365C1 (en) |
SG (1) | SG59939A1 (en) |
SK (1) | SK52693A3 (en) |
WO (1) | WO1992009679A1 (en) |
Families Citing this family (41)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
FR2647741B1 (en) * | 1989-05-31 | 1991-08-23 | Bendix France | METHOD FOR ADJUSTING THE JUMP VALUE OF A BRAKE ASSIST MOTOR |
DE4017463A1 (en) * | 1990-05-30 | 1991-12-05 | Henkel Kgaa | PROCESS FOR MANUFACTURING HIGHLY CONCENTRATED PASTS OF ALPHA-SULF-FATTY-ALKYLESTER-ALKALI-METAL SALT |
CA2113564A1 (en) * | 1991-07-15 | 1993-02-04 | James E. Taneri | A personal cleansing freezer bar made with a rigid, interlocking mesh of neutralized carboxylic acid |
US5262079A (en) * | 1992-03-20 | 1993-11-16 | The Procter & Gamble Company | Framed neutral pH cleansing bar |
US5227086A (en) * | 1992-03-20 | 1993-07-13 | The Procter & Gamble Company | Framed skin pH cleansing bar |
EP0670885B1 (en) * | 1992-11-30 | 1997-08-20 | The Procter & Gamble Company | High sudsing detergent compositions with specially selected soaps |
CA2147674C (en) * | 1994-05-16 | 1999-03-30 | David Robert Zint | Shaped semi-solid or solid dishwashing detergent |
WO1997022684A1 (en) * | 1995-12-20 | 1997-06-26 | The Procter & Gamble Company | Pour molded personal cleansing bar |
WO1998011864A2 (en) * | 1996-09-23 | 1998-03-26 | The Procter & Gamble Company | Lathering and cleansing personal cleansing bar compositions which contain elongated lipid particles |
JPH10512921A (en) * | 1996-10-11 | 1998-12-08 | ザ、プロクター、エンド、ギャンブル、カンパニー | Laundry solid compositions comprising dihydric alcohols for improving physical properties |
JP3227694B2 (en) * | 1996-12-11 | 2001-11-12 | 花王株式会社 | Framed soap composition |
WO1998027193A1 (en) * | 1996-12-16 | 1998-06-25 | The Procter & Gamble Company | Personal cleansing bar composition containing sodium lauroyl lactylate |
US6680285B2 (en) * | 2000-12-21 | 2004-01-20 | Unilever Home & Personal Care Usa A Division Of Conopco, Inc. | Skin cleansing bar with high levels of liquid emollient |
US6630432B2 (en) * | 2001-04-18 | 2003-10-07 | Unilever Home & Personal Care Usa, Division Of Conopco | Processable soap based bars comprising soaps of α hydroxy acid and minimum amount of free fatty acid and/or monoglyceride |
PL199102B1 (en) * | 2001-05-03 | 2008-08-29 | Unilever Nv | Shaped solid detergent compositions |
AU2003227048A1 (en) * | 2002-04-02 | 2003-10-13 | Unilever N.V. | Detergent bar compositions |
US6664217B1 (en) * | 2002-07-18 | 2003-12-16 | Unilever Home & Personal Care, Usa Division Of Conopco, Inc. | Toilet bar having simultaneous exfoliating and moisturizing properties |
WO2004029058A1 (en) * | 2002-09-25 | 2004-04-08 | Sankyo Company, Limited | Medicinal composition for inhibiting increase in blood gastrin concentration |
DE10346954A1 (en) * | 2003-10-09 | 2005-06-09 | Beiersdorf Ag | Temperature-stable cosmetic cleaning preparation with dicarboxylic acids |
US7045491B2 (en) * | 2003-10-28 | 2006-05-16 | Colgate-Palmolive Company | Bar soap composition with reduced bar wear properties |
JP5367494B2 (en) * | 2009-08-06 | 2013-12-11 | 花王株式会社 | Manufacturing method of frame kneaded soap |
BR112015000666A2 (en) | 2012-07-23 | 2017-08-08 | Unilever Nv | manufacturing process of ground and compacted soap composition. |
CN106544157A (en) * | 2016-11-02 | 2017-03-29 | 广州精点高分子材料制品有限公司 | A kind of beauty facial soap and preparation method thereof |
CN107245391A (en) * | 2016-12-25 | 2017-10-13 | 池州市建东生物科技有限公司 | A kind of special soap of skin disease |
CA3089624A1 (en) | 2018-01-26 | 2019-08-01 | Ecolab Usa Inc. | Solidifying liquid amine oxide, betaine, and/or sultaine surfactants with a binder and optional carrier |
CN111655828A (en) | 2018-01-26 | 2020-09-11 | 埃科莱布美国股份有限公司 | Curing liquid amine oxide, betaine and/or sulfobetaine surfactants with a carrier |
WO2019148071A1 (en) | 2018-01-26 | 2019-08-01 | Ecolab Usa Inc. | Solidifying liquid anionic surfactants |
US12122979B2 (en) | 2020-04-10 | 2024-10-22 | The Procter & Gamble Company | Cleaning article with preferential rheological solid composition |
CN115443120A (en) | 2020-04-10 | 2022-12-06 | 宝洁公司 | rheological solid composition |
WO2021207438A1 (en) * | 2020-04-10 | 2021-10-14 | The Procter & Gamble Company | Oral care product comprising a rheological solid composition |
EP4132457A1 (en) | 2020-04-10 | 2023-02-15 | The Procter & Gamble Company | Rheological solid composition |
CA3169684A1 (en) | 2020-04-10 | 2021-10-28 | The Procter & Gamble Company | Cleaning implement with a rheological solid composition |
EP4132476A1 (en) | 2020-04-10 | 2023-02-15 | The Procter & Gamble Company | Rheological solid oral composition |
US11833237B2 (en) | 2021-03-09 | 2023-12-05 | The Procter & Gamble Company | Method for enhancing scalp active deposition |
EP4098243A1 (en) * | 2021-05-31 | 2022-12-07 | BIC Violex Single Member S.A. | Solid shaving aid composition |
MX2024006096A (en) * | 2022-08-12 | 2024-05-30 | Procter & Gamble | SOLID DISSOLUBLE COMPOSITIONS. |
WO2024036122A1 (en) * | 2022-08-12 | 2024-02-15 | The Procter & Gamble Company | Solid dissolvable compositions |
US20240060015A1 (en) * | 2022-08-12 | 2024-02-22 | The Procter & Gamble Company | Solid dissolvable compositions |
EP4569066A1 (en) * | 2022-08-12 | 2025-06-18 | The Procter & Gamble Company | Low-water compositions |
JP2024543276A (en) * | 2022-08-12 | 2024-11-20 | ザ プロクター アンド ギャンブル カンパニー | Solid soluble composition |
JP2024543599A (en) * | 2022-08-12 | 2024-11-21 | ザ プロクター アンド ギャンブル カンパニー | Low moisture composition |
Family Cites Families (9)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US3226329A (en) * | 1961-09-14 | 1965-12-28 | Procter & Gamble | Germicidal cleansing composition |
DE2132035C3 (en) * | 1971-06-28 | 1979-08-30 | Henkel Kgaa, 4000 Duesseldorf | Molded detergent composition |
US3793214A (en) * | 1971-10-22 | 1974-02-19 | Avon Prod Inc | Transparent soap composition |
US4396521A (en) * | 1976-04-22 | 1983-08-02 | Giuseppe Borrello | Solid detergent spotter |
US4165293A (en) * | 1977-05-16 | 1979-08-21 | Amway Corporation | Solid transparent cleanser |
DE3246796A1 (en) * | 1981-12-23 | 1983-07-21 | Colgate-Palmolive Co., 10022 New York, N.Y. | Crack-free soap bar |
US4851147A (en) * | 1987-02-26 | 1989-07-25 | Finetex, Inc. | Transparent combination soap-synthetic detergent bar |
US4758370A (en) * | 1987-04-30 | 1988-07-19 | Neutrogena Corp. | Compositions and processes for the continuous production of transparent soap |
ES2063043T3 (en) * | 1987-09-17 | 1995-01-01 | Procter & Gamble | TOILET BAR FOR ULTRA-CLEAN SKIN CLEANING WITH SELECTED MIXED POLYMERS. |
-
1991
- 1991-11-20 SK SK526-93A patent/SK52693A3/en unknown
- 1991-11-20 CA CA002095351A patent/CA2095351C/en not_active Expired - Fee Related
- 1991-11-20 EP EP92904074A patent/EP0559837B1/en not_active Expired - Lifetime
- 1991-11-20 ES ES92904074T patent/ES2079180T3/en not_active Expired - Lifetime
- 1991-11-20 SG SG1996003227A patent/SG59939A1/en unknown
- 1991-11-20 FI FI932366A patent/FI932366A0/en not_active Application Discontinuation
- 1991-11-20 DK DK92904074.9T patent/DK0559837T3/en active
- 1991-11-20 HU HU9301532A patent/HU215484B/en not_active IP Right Cessation
- 1991-11-20 BR BR919107125A patent/BR9107125A/en not_active IP Right Cessation
- 1991-11-20 AT AT92904074T patent/ATE129522T1/en not_active IP Right Cessation
- 1991-11-20 DE DE69114143T patent/DE69114143T2/en not_active Expired - Fee Related
- 1991-11-20 RU RU9193042103A patent/RU2080365C1/en active
- 1991-11-20 JP JP4504274A patent/JPH06503122A/en active Pending
- 1991-11-20 AU AU91763/91A patent/AU657295B2/en not_active Ceased
- 1991-11-20 CZ CS93987A patent/CZ283495B6/en not_active IP Right Cessation
- 1991-11-20 WO PCT/US1991/008733 patent/WO1992009679A1/en active IP Right Grant
- 1991-11-25 NZ NZ240709A patent/NZ240709A/en unknown
- 1991-11-25 IE IE409491A patent/IE72087B1/en not_active IP Right Cessation
- 1991-11-25 AR AR91321225A patent/AR247426A1/en active
- 1991-11-26 PT PT99606A patent/PT99606A/en not_active Application Discontinuation
- 1991-11-26 EG EG72291A patent/EG19580A/en active
- 1991-11-26 CN CN91111928A patent/CN1036529C/en not_active Expired - Fee Related
- 1991-11-26 MX MX9102229A patent/MX9102229A/en not_active IP Right Cessation
- 1991-11-26 MA MA22633A patent/MA22349A1/en unknown
-
1993
- 1993-05-21 NO NO93931848A patent/NO931848L/en unknown
- 1993-05-25 KR KR1019930701554A patent/KR100226393B1/en not_active Expired - Fee Related
-
1995
- 1995-10-26 GR GR950402864T patent/GR3017892T3/en unknown
Also Published As
Similar Documents
Publication | Publication Date | Title |
---|---|---|
CA2095351C (en) | Shaped solid made with a rigid, interlocking mesh of neutralized carboxylic acid | |
US5340492A (en) | Shaped solid made with a rigid, interlocking mesh of neutralized carboxylic acid | |
CA2131308C (en) | Neutral ph cleansing bar | |
EP0631614B1 (en) | SKIN pH CLEANSING BAR | |
US5425892A (en) | Personal cleansing freezer bar made with a rigid, interlocking mesh of neutralized carboxylic acid | |
US5225097A (en) | Skin pH freezer bar and process | |
US5264144A (en) | Freezer personal cleansing bar with selected fatty acid soaps for improved mildness and good lather | |
US5264145A (en) | Personal cleansing freezer bar with selected fatty acid soaps and synthetic surfactant for reduced bathtub ring, improved mildness, and good lather | |
US5225098A (en) | Neutral pH freezer bar and process | |
US5494612A (en) | Process for producing detergent bar with low soap composition having optimal throughput at lower temperatures | |
HK1006179B (en) | Shaped solid made with a rigid, interlocking mesh of neutralized carboxylic acid | |
NZ248471A (en) | A "freezer" soap bar comprising mostly na and k soaps of: myristic, palmitic and stearic acids plus oleic and/or lauric acid and/or minor fatty acid soap; water; and optionally a lathering synthetic surfactant and a sugar |
Legal Events
Date | Code | Title | Description |
---|---|---|---|
EEER | Examination request | ||
MKLA | Lapsed |