DE19915837A1 - Aqueous multiphase surfactant preparations - Google Patents
Aqueous multiphase surfactant preparationsInfo
- Publication number
- DE19915837A1 DE19915837A1 DE19915837A DE19915837A DE19915837A1 DE 19915837 A1 DE19915837 A1 DE 19915837A1 DE 19915837 A DE19915837 A DE 19915837A DE 19915837 A DE19915837 A DE 19915837A DE 19915837 A1 DE19915837 A1 DE 19915837A1
- Authority
- DE
- Germany
- Prior art keywords
- aqueous
- phases
- aqueous preparations
- soluble
- preparations according
- 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.)
- Withdrawn
Links
- 238000002360 preparation method Methods 0.000 title claims abstract description 31
- 239000004094 surface-active agent Substances 0.000 title claims abstract description 17
- 150000001875 compounds Chemical class 0.000 claims abstract description 25
- 229920000642 polymer Polymers 0.000 claims abstract description 20
- -1 dextrane Polymers 0.000 claims abstract description 18
- RTZKZFJDLAIYFH-UHFFFAOYSA-N Diethyl ether Chemical compound CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 claims abstract description 15
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 claims abstract description 15
- 239000012071 phase Substances 0.000 claims abstract description 14
- KFZMGEQAYNKOFK-UHFFFAOYSA-N Isopropanol Chemical compound CC(C)O KFZMGEQAYNKOFK-UHFFFAOYSA-N 0.000 claims abstract description 10
- 239000008346 aqueous phase Substances 0.000 claims abstract description 10
- 125000004432 carbon atom Chemical group C* 0.000 claims abstract description 8
- 229920003086 cellulose ether Polymers 0.000 claims abstract description 7
- 229920001451 polypropylene glycol Polymers 0.000 claims abstract description 7
- 229920000663 Hydroxyethyl cellulose Polymers 0.000 claims abstract description 6
- 235000019447 hydroxyethyl cellulose Nutrition 0.000 claims abstract description 6
- 239000000230 xanthan gum Substances 0.000 claims abstract description 6
- 229920001285 xanthan gum Polymers 0.000 claims abstract description 6
- 235000010493 xanthan gum Nutrition 0.000 claims abstract description 6
- 229940082509 xanthan gum Drugs 0.000 claims abstract description 6
- 125000002091 cationic group Chemical group 0.000 claims abstract description 5
- 238000005191 phase separation Methods 0.000 claims abstract description 5
- 239000004354 Hydroxyethyl cellulose Substances 0.000 claims abstract description 4
- 229920002385 Sodium hyaluronate Polymers 0.000 claims abstract description 4
- 229940010747 sodium hyaluronate Drugs 0.000 claims abstract description 4
- YWIVKILSMZOHHF-QJZPQSOGSA-N sodium;(2s,3s,4s,5r,6r)-6-[(2s,3r,4r,5s,6r)-3-acetamido-2-[(2s,3s,4r,5r,6r)-6-[(2r,3r,4r,5s,6r)-3-acetamido-2,5-dihydroxy-6-(hydroxymethyl)oxan-4-yl]oxy-2-carboxy-4,5-dihydroxyoxan-3-yl]oxy-5-hydroxy-6-(hydroxymethyl)oxan-4-yl]oxy-3,4,5-trihydroxyoxane-2- Chemical compound [Na+].CC(=O)N[C@H]1[C@H](O)O[C@H](CO)[C@@H](O)[C@@H]1O[C@H]1[C@H](O)[C@@H](O)[C@H](O[C@H]2[C@@H]([C@@H](O[C@H]3[C@@H]([C@@H](O)[C@H](O)[C@H](O3)C(O)=O)O)[C@H](O)[C@@H](CO)O2)NC(C)=O)[C@@H](C(O)=O)O1 YWIVKILSMZOHHF-QJZPQSOGSA-N 0.000 claims abstract description 4
- 125000000217 alkyl group Chemical group 0.000 claims description 10
- 150000003839 salts Chemical class 0.000 claims description 9
- 239000000203 mixture Substances 0.000 claims description 8
- 229920000151 polyglycol Polymers 0.000 claims description 7
- 239000010695 polyglycol Substances 0.000 claims description 7
- MTHSVFCYNBDYFN-UHFFFAOYSA-N diethylene glycol Chemical group OCCOCCO MTHSVFCYNBDYFN-UHFFFAOYSA-N 0.000 claims description 6
- 229920002307 Dextran Polymers 0.000 claims description 5
- 239000000975 dye Substances 0.000 claims description 5
- 239000003792 electrolyte Substances 0.000 claims description 4
- 150000005846 sugar alcohols Polymers 0.000 claims description 4
- FZWBNHMXJMCXLU-BLAUPYHCSA-N isomaltotriose Chemical compound 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](O)[C@@H](O)[C@@H](OC[C@@H](O)[C@@H](O)[C@H](O)[C@@H](O)C=O)O1 FZWBNHMXJMCXLU-BLAUPYHCSA-N 0.000 claims description 3
- 229960002086 dextran Drugs 0.000 claims description 2
- 229940071826 hydroxyethyl cellulose Drugs 0.000 claims 1
- 235000019441 ethanol Nutrition 0.000 abstract description 10
- QAOWNCQODCNURD-UHFFFAOYSA-L Sulfate Chemical compound [O-]S([O-])(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-L 0.000 abstract description 3
- ULUAUXLGCMPNKK-UHFFFAOYSA-N Sulfobutanedioic acid Chemical compound OC(=O)CC(C(O)=O)S(O)(=O)=O ULUAUXLGCMPNKK-UHFFFAOYSA-N 0.000 abstract description 2
- 235000002639 sodium chloride Nutrition 0.000 description 12
- 239000012459 cleaning agent Substances 0.000 description 6
- 239000002537 cosmetic Substances 0.000 description 6
- 235000014113 dietary fatty acids Nutrition 0.000 description 5
- 239000000194 fatty acid Substances 0.000 description 5
- 229930195729 fatty acid Natural products 0.000 description 5
- 239000007788 liquid Substances 0.000 description 5
- 238000004140 cleaning Methods 0.000 description 4
- KWIUHFFTVRNATP-UHFFFAOYSA-N glycine betaine Chemical compound C[N+](C)(C)CC([O-])=O KWIUHFFTVRNATP-UHFFFAOYSA-N 0.000 description 4
- 238000000926 separation method Methods 0.000 description 4
- LYCAIKOWRPUZTN-UHFFFAOYSA-N Ethylene glycol Chemical compound OCCO LYCAIKOWRPUZTN-UHFFFAOYSA-N 0.000 description 3
- PEDCQBHIVMGVHV-UHFFFAOYSA-N Glycerine Chemical compound OCC(O)CO PEDCQBHIVMGVHV-UHFFFAOYSA-N 0.000 description 3
- FAPWRFPIFSIZLT-UHFFFAOYSA-M Sodium chloride Chemical compound [Na+].[Cl-] FAPWRFPIFSIZLT-UHFFFAOYSA-M 0.000 description 3
- 239000013543 active substance Substances 0.000 description 3
- 230000000694 effects Effects 0.000 description 3
- 229920005862 polyol Polymers 0.000 description 3
- 150000003077 polyols Chemical group 0.000 description 3
- BDERNNFJNOPAEC-UHFFFAOYSA-N propan-1-ol Chemical compound CCCO BDERNNFJNOPAEC-UHFFFAOYSA-N 0.000 description 3
- 235000012752 quinoline yellow Nutrition 0.000 description 3
- 239000004172 quinoline yellow Substances 0.000 description 3
- 238000005204 segregation Methods 0.000 description 3
- 239000011734 sodium Substances 0.000 description 3
- KIUKXJAPPMFGSW-DNGZLQJQSA-N (2S,3S,4S,5R,6R)-6-[(2S,3R,4R,5S,6R)-3-Acetamido-2-[(2S,3S,4R,5R,6R)-6-[(2R,3R,4R,5S,6R)-3-acetamido-2,5-dihydroxy-6-(hydroxymethyl)oxan-4-yl]oxy-2-carboxy-4,5-dihydroxyoxan-3-yl]oxy-5-hydroxy-6-(hydroxymethyl)oxan-4-yl]oxy-3,4,5-trihydroxyoxane-2-carboxylic acid Chemical compound CC(=O)N[C@H]1[C@H](O)O[C@H](CO)[C@@H](O)[C@@H]1O[C@H]1[C@H](O)[C@@H](O)[C@H](O[C@H]2[C@@H]([C@@H](O[C@H]3[C@@H]([C@@H](O)[C@H](O)[C@H](O3)C(O)=O)O)[C@H](O)[C@@H](CO)O2)NC(C)=O)[C@@H](C(O)=O)O1 KIUKXJAPPMFGSW-DNGZLQJQSA-N 0.000 description 2
- ITYXXSSJBOAGAR-UHFFFAOYSA-N 1-(methylamino)-4-(4-methylanilino)anthracene-9,10-dione Chemical compound C1=2C(=O)C3=CC=CC=C3C(=O)C=2C(NC)=CC=C1NC1=CC=C(C)C=C1 ITYXXSSJBOAGAR-UHFFFAOYSA-N 0.000 description 2
- 244000007835 Cyamopsis tetragonoloba Species 0.000 description 2
- FYYHWMGAXLPEAU-UHFFFAOYSA-N Magnesium Chemical compound [Mg] FYYHWMGAXLPEAU-UHFFFAOYSA-N 0.000 description 2
- TWRXJAOTZQYOKJ-UHFFFAOYSA-L Magnesium chloride Chemical compound [Mg+2].[Cl-].[Cl-] TWRXJAOTZQYOKJ-UHFFFAOYSA-L 0.000 description 2
- DNIAPMSPPWPWGF-UHFFFAOYSA-N Propylene glycol Chemical compound CC(O)CO DNIAPMSPPWPWGF-UHFFFAOYSA-N 0.000 description 2
- 229920002472 Starch Polymers 0.000 description 2
- 239000002253 acid Substances 0.000 description 2
- 150000001298 alcohols Chemical class 0.000 description 2
- 229910052783 alkali metal Inorganic materials 0.000 description 2
- 150000001340 alkali metals Chemical class 0.000 description 2
- 239000003945 anionic surfactant Substances 0.000 description 2
- 229960003237 betaine Drugs 0.000 description 2
- WERYXYBDKMZEQL-UHFFFAOYSA-N butane-1,4-diol Chemical compound OCCCCO WERYXYBDKMZEQL-UHFFFAOYSA-N 0.000 description 2
- 229920002678 cellulose Polymers 0.000 description 2
- 239000001913 cellulose Substances 0.000 description 2
- 235000010980 cellulose Nutrition 0.000 description 2
- 150000002009 diols Chemical class 0.000 description 2
- HNRMPXKDFBEGFZ-UHFFFAOYSA-N ethyl trimethyl methane Natural products CCC(C)(C)C HNRMPXKDFBEGFZ-UHFFFAOYSA-N 0.000 description 2
- 239000000576 food coloring agent Substances 0.000 description 2
- 150000004676 glycans Chemical class 0.000 description 2
- 229920002674 hyaluronan Polymers 0.000 description 2
- 229960003160 hyaluronic acid Drugs 0.000 description 2
- ZXEKIIBDNHEJCQ-UHFFFAOYSA-N isobutanol Chemical compound CC(C)CO ZXEKIIBDNHEJCQ-UHFFFAOYSA-N 0.000 description 2
- 125000003473 lipid group Chemical group 0.000 description 2
- 229910052749 magnesium Inorganic materials 0.000 description 2
- 239000011777 magnesium Substances 0.000 description 2
- HOVAGTYPODGVJG-UHFFFAOYSA-N methyl beta-galactoside Natural products COC1OC(CO)C(O)C(O)C1O HOVAGTYPODGVJG-UHFFFAOYSA-N 0.000 description 2
- 229920005615 natural polymer Polymers 0.000 description 2
- 239000003921 oil Substances 0.000 description 2
- 229920001282 polysaccharide Polymers 0.000 description 2
- 239000005017 polysaccharide Substances 0.000 description 2
- 108090000623 proteins and genes Proteins 0.000 description 2
- 102000004169 proteins and genes Human genes 0.000 description 2
- 229940051201 quinoline yellow Drugs 0.000 description 2
- IZMJMCDDWKSTTK-UHFFFAOYSA-N quinoline yellow Chemical compound C1=CC=CC2=NC(C3C(C4=CC=CC=C4C3=O)=O)=CC=C21 IZMJMCDDWKSTTK-UHFFFAOYSA-N 0.000 description 2
- 239000002453 shampoo Substances 0.000 description 2
- 239000000344 soap Substances 0.000 description 2
- 239000011780 sodium chloride Substances 0.000 description 2
- 239000000243 solution Substances 0.000 description 2
- 239000008107 starch Substances 0.000 description 2
- 235000019698 starch Nutrition 0.000 description 2
- BDHFUVZGWQCTTF-UHFFFAOYSA-M sulfonate Chemical compound [O-]S(=O)=O BDHFUVZGWQCTTF-UHFFFAOYSA-M 0.000 description 2
- 239000001577 tetrasodium phosphonato phosphate Substances 0.000 description 2
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 2
- BZANQLIRVMZFOS-ZKZCYXTQSA-N (3r,4s,5s,6r)-2-butoxy-6-(hydroxymethyl)oxane-3,4,5-triol Chemical compound CCCCOC1O[C@H](CO)[C@@H](O)[C@H](O)[C@H]1O BZANQLIRVMZFOS-ZKZCYXTQSA-N 0.000 description 1
- HOVAGTYPODGVJG-UVSYOFPXSA-N (3s,5r)-2-(hydroxymethyl)-6-methoxyoxane-3,4,5-triol Chemical compound COC1OC(CO)[C@@H](O)C(O)[C@H]1O HOVAGTYPODGVJG-UVSYOFPXSA-N 0.000 description 1
- SMZOUWXMTYCWNB-UHFFFAOYSA-N 2-(2-methoxy-5-methylphenyl)ethanamine Chemical compound COC1=CC=C(C)C=C1CCN SMZOUWXMTYCWNB-UHFFFAOYSA-N 0.000 description 1
- XNWFRZJHXBZDAG-UHFFFAOYSA-N 2-METHOXYETHANOL Chemical compound COCCO XNWFRZJHXBZDAG-UHFFFAOYSA-N 0.000 description 1
- NIXOWILDQLNWCW-UHFFFAOYSA-N 2-Propenoic acid Natural products OC(=O)C=C NIXOWILDQLNWCW-UHFFFAOYSA-N 0.000 description 1
- TURPNXCLLLFJAP-UHFFFAOYSA-N 2-[2-(2-hydroxyethoxy)ethoxy]ethyl hydrogen sulfate Chemical compound OCCOCCOCCOS(O)(=O)=O TURPNXCLLLFJAP-UHFFFAOYSA-N 0.000 description 1
- ZNQVEEAIQZEUHB-UHFFFAOYSA-N 2-ethoxyethanol Chemical compound CCOCCO ZNQVEEAIQZEUHB-UHFFFAOYSA-N 0.000 description 1
- 229940093475 2-ethoxyethanol Drugs 0.000 description 1
- PSJBSUHYCGQTHZ-UHFFFAOYSA-N 3-Methoxy-1,2-propanediol Chemical compound COCC(O)CO PSJBSUHYCGQTHZ-UHFFFAOYSA-N 0.000 description 1
- AGNTUZCMJBTHOG-UHFFFAOYSA-N 3-[3-(2,3-dihydroxypropoxy)-2-hydroxypropoxy]propane-1,2-diol Chemical compound OCC(O)COCC(O)COCC(O)CO AGNTUZCMJBTHOG-UHFFFAOYSA-N 0.000 description 1
- CYDQOEWLBCCFJZ-UHFFFAOYSA-N 4-(4-fluorophenyl)oxane-4-carboxylic acid Chemical compound C=1C=C(F)C=CC=1C1(C(=O)O)CCOCC1 CYDQOEWLBCCFJZ-UHFFFAOYSA-N 0.000 description 1
- HRPVXLWXLXDGHG-UHFFFAOYSA-N Acrylamide Chemical compound NC(=O)C=C HRPVXLWXLXDGHG-UHFFFAOYSA-N 0.000 description 1
- 102000009027 Albumins Human genes 0.000 description 1
- 108010088751 Albumins Proteins 0.000 description 1
- OYPRJOBELJOOCE-UHFFFAOYSA-N Calcium Chemical compound [Ca] OYPRJOBELJOOCE-UHFFFAOYSA-N 0.000 description 1
- KXDHJXZQYSOELW-UHFFFAOYSA-N Carbamic acid Chemical compound NC(O)=O KXDHJXZQYSOELW-UHFFFAOYSA-N 0.000 description 1
- 229920002134 Carboxymethyl cellulose Polymers 0.000 description 1
- 229920001661 Chitosan Polymers 0.000 description 1
- VEXZGXHMUGYJMC-UHFFFAOYSA-M Chloride anion Chemical compound [Cl-] VEXZGXHMUGYJMC-UHFFFAOYSA-M 0.000 description 1
- FBPFZTCFMRRESA-FSIIMWSLSA-N D-Glucitol Natural products OC[C@H](O)[C@H](O)[C@@H](O)[C@H](O)CO FBPFZTCFMRRESA-FSIIMWSLSA-N 0.000 description 1
- 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 1
- 239000004386 Erythritol Substances 0.000 description 1
- UNXHWFMMPAWVPI-UHFFFAOYSA-N Erythritol Natural products OCC(O)C(O)CO UNXHWFMMPAWVPI-UHFFFAOYSA-N 0.000 description 1
- IAYPIBMASNFSPL-UHFFFAOYSA-N Ethylene oxide Chemical class C1CO1 IAYPIBMASNFSPL-UHFFFAOYSA-N 0.000 description 1
- 108010010803 Gelatin Proteins 0.000 description 1
- 229920002683 Glycosaminoglycan Polymers 0.000 description 1
- 229920001479 Hydroxyethyl methyl cellulose Polymers 0.000 description 1
- 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 description 1
- LRHPLDYGYMQRHN-UHFFFAOYSA-N N-Butanol Chemical compound CCCCO LRHPLDYGYMQRHN-UHFFFAOYSA-N 0.000 description 1
- WHNWPMSKXPGLAX-UHFFFAOYSA-N N-Vinyl-2-pyrrolidone Chemical class C=CN1CCCC1=O WHNWPMSKXPGLAX-UHFFFAOYSA-N 0.000 description 1
- 229910019142 PO4 Inorganic materials 0.000 description 1
- ALQSHHUCVQOPAS-UHFFFAOYSA-N Pentane-1,5-diol Chemical compound OCCCCCO ALQSHHUCVQOPAS-UHFFFAOYSA-N 0.000 description 1
- 239000004721 Polyphenylene oxide Chemical group 0.000 description 1
- 239000004373 Pullulan Substances 0.000 description 1
- 229920001218 Pullulan Polymers 0.000 description 1
- VMHLLURERBWHNL-UHFFFAOYSA-M Sodium acetate Chemical compound [Na+].CC([O-])=O VMHLLURERBWHNL-UHFFFAOYSA-M 0.000 description 1
- UIIMBOGNXHQVGW-DEQYMQKBSA-M Sodium bicarbonate-14C Chemical compound [Na+].O[14C]([O-])=O UIIMBOGNXHQVGW-DEQYMQKBSA-M 0.000 description 1
- 230000001133 acceleration Effects 0.000 description 1
- 150000007513 acids Chemical class 0.000 description 1
- 239000000654 additive Substances 0.000 description 1
- 239000003513 alkali Substances 0.000 description 1
- 150000008051 alkyl sulfates Chemical class 0.000 description 1
- 150000008052 alkyl sulfonates Chemical class 0.000 description 1
- 150000003863 ammonium salts Chemical class 0.000 description 1
- 239000002280 amphoteric surfactant Substances 0.000 description 1
- 125000000129 anionic group Chemical group 0.000 description 1
- 239000003963 antioxidant agent Substances 0.000 description 1
- 239000007864 aqueous solution Substances 0.000 description 1
- 230000009286 beneficial effect Effects 0.000 description 1
- 229920001222 biopolymer Polymers 0.000 description 1
- 239000001045 blue dye Substances 0.000 description 1
- 239000000337 buffer salt Substances 0.000 description 1
- 239000001110 calcium chloride Substances 0.000 description 1
- 229910001628 calcium chloride Inorganic materials 0.000 description 1
- 125000003178 carboxy group Chemical group [H]OC(*)=O 0.000 description 1
- 235000010948 carboxy methyl cellulose Nutrition 0.000 description 1
- 238000004040 coloring Methods 0.000 description 1
- 239000008139 complexing agent Substances 0.000 description 1
- 229920001577 copolymer Polymers 0.000 description 1
- PDXRQENMIVHKPI-UHFFFAOYSA-N cyclohexane-1,1-diol Chemical compound OC1(O)CCCCC1 PDXRQENMIVHKPI-UHFFFAOYSA-N 0.000 description 1
- 230000001419 dependent effect Effects 0.000 description 1
- 239000003599 detergent Substances 0.000 description 1
- GPLRAVKSCUXZTP-UHFFFAOYSA-N diglycerol Chemical compound OCC(O)COCC(O)CO GPLRAVKSCUXZTP-UHFFFAOYSA-N 0.000 description 1
- SZXQTJUDPRGNJN-UHFFFAOYSA-N dipropylene glycol Chemical compound OCCCOCCCO SZXQTJUDPRGNJN-UHFFFAOYSA-N 0.000 description 1
- BNIILDVGGAEEIG-UHFFFAOYSA-L disodium hydrogen phosphate Chemical compound [Na+].[Na+].OP([O-])([O-])=O BNIILDVGGAEEIG-UHFFFAOYSA-L 0.000 description 1
- 229910000397 disodium phosphate Inorganic materials 0.000 description 1
- 235000019800 disodium phosphate Nutrition 0.000 description 1
- UNXHWFMMPAWVPI-ZXZARUISSA-N erythritol Chemical compound OC[C@H](O)[C@H](O)CO UNXHWFMMPAWVPI-ZXZARUISSA-N 0.000 description 1
- 229940009714 erythritol Drugs 0.000 description 1
- 235000019414 erythritol Nutrition 0.000 description 1
- 239000004744 fabric Substances 0.000 description 1
- 150000004665 fatty acids Chemical class 0.000 description 1
- 150000002191 fatty alcohols Chemical class 0.000 description 1
- 238000005187 foaming Methods 0.000 description 1
- 239000003205 fragrance Substances 0.000 description 1
- 229920000159 gelatin Polymers 0.000 description 1
- 235000019322 gelatine Nutrition 0.000 description 1
- 235000011852 gelatine desserts Nutrition 0.000 description 1
- 229930182478 glucoside Natural products 0.000 description 1
- 150000004820 halides Chemical class 0.000 description 1
- XXMIOPMDWAUFGU-UHFFFAOYSA-N hexane-1,6-diol Chemical compound OCCCCCCO XXMIOPMDWAUFGU-UHFFFAOYSA-N 0.000 description 1
- 230000006266 hibernation Effects 0.000 description 1
- 229920006158 high molecular weight polymer Polymers 0.000 description 1
- 150000008040 ionic compounds Chemical class 0.000 description 1
- 239000004922 lacquer Substances 0.000 description 1
- 150000002632 lipids Chemical class 0.000 description 1
- 235000001055 magnesium Nutrition 0.000 description 1
- 229910001629 magnesium chloride Inorganic materials 0.000 description 1
- 229920000609 methyl cellulose Polymers 0.000 description 1
- 235000010981 methylcellulose Nutrition 0.000 description 1
- 239000000178 monomer Substances 0.000 description 1
- 239000002736 nonionic surfactant Substances 0.000 description 1
- 239000007764 o/w emulsion Substances 0.000 description 1
- 239000003002 pH adjusting agent Substances 0.000 description 1
- WXZMFSXDPGVJKK-UHFFFAOYSA-N pentaerythritol Chemical compound OCC(CO)(CO)CO WXZMFSXDPGVJKK-UHFFFAOYSA-N 0.000 description 1
- 235000021317 phosphate Nutrition 0.000 description 1
- 150000003013 phosphoric acid derivatives Chemical class 0.000 description 1
- 229920002401 polyacrylamide Polymers 0.000 description 1
- 229920001515 polyalkylene glycol Polymers 0.000 description 1
- 229920000570 polyether Chemical group 0.000 description 1
- 229920002451 polyvinyl alcohol Polymers 0.000 description 1
- 235000019422 polyvinyl alcohol Nutrition 0.000 description 1
- 229920000036 polyvinylpyrrolidone Polymers 0.000 description 1
- 239000001267 polyvinylpyrrolidone Substances 0.000 description 1
- 235000013855 polyvinylpyrrolidone Nutrition 0.000 description 1
- 239000004175 ponceau 4R Substances 0.000 description 1
- 239000003755 preservative agent Substances 0.000 description 1
- 235000019423 pullulan Nutrition 0.000 description 1
- 125000001453 quaternary ammonium group Chemical group 0.000 description 1
- 239000002994 raw material Substances 0.000 description 1
- 229910052708 sodium Inorganic materials 0.000 description 1
- 239000001632 sodium acetate Substances 0.000 description 1
- 235000017281 sodium acetate Nutrition 0.000 description 1
- WXMKPNITSTVMEF-UHFFFAOYSA-M sodium benzoate Chemical compound [Na+].[O-]C(=O)C1=CC=CC=C1 WXMKPNITSTVMEF-UHFFFAOYSA-M 0.000 description 1
- 239000004299 sodium benzoate Substances 0.000 description 1
- 235000010234 sodium benzoate Nutrition 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
- 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 1
- GCLGEJMYGQKIIW-UHFFFAOYSA-H sodium hexametaphosphate Chemical compound [Na]OP1(=O)OP(=O)(O[Na])OP(=O)(O[Na])OP(=O)(O[Na])OP(=O)(O[Na])OP(=O)(O[Na])O1 GCLGEJMYGQKIIW-UHFFFAOYSA-H 0.000 description 1
- 235000019982 sodium hexametaphosphate Nutrition 0.000 description 1
- 239000001540 sodium lactate Substances 0.000 description 1
- 229940005581 sodium lactate Drugs 0.000 description 1
- 235000011088 sodium lactate Nutrition 0.000 description 1
- 229940048086 sodium pyrophosphate Drugs 0.000 description 1
- 159000000000 sodium salts Chemical class 0.000 description 1
- 229940048842 sodium xylenesulfonate Drugs 0.000 description 1
- QUCDWLYKDRVKMI-UHFFFAOYSA-M sodium;3,4-dimethylbenzenesulfonate Chemical compound [Na+].CC1=CC=C(S([O-])(=O)=O)C=C1C QUCDWLYKDRVKMI-UHFFFAOYSA-M 0.000 description 1
- KVCGISUBCHHTDD-UHFFFAOYSA-M sodium;4-methylbenzenesulfonate Chemical compound [Na+].CC1=CC=C(S([O-])(=O)=O)C=C1 KVCGISUBCHHTDD-UHFFFAOYSA-M 0.000 description 1
- 239000000600 sorbitol Substances 0.000 description 1
- 239000000126 substance Substances 0.000 description 1
- 238000006467 substitution reaction Methods 0.000 description 1
- IIACRCGMVDHOTQ-UHFFFAOYSA-N sulfamic acid Chemical group NS(O)(=O)=O IIACRCGMVDHOTQ-UHFFFAOYSA-N 0.000 description 1
- 150000008054 sulfonate salts Chemical class 0.000 description 1
- 150000003467 sulfuric acid derivatives Chemical class 0.000 description 1
- 229920001059 synthetic polymer Polymers 0.000 description 1
- 235000019818 tetrasodium diphosphate Nutrition 0.000 description 1
- ZIBGPFATKBEMQZ-UHFFFAOYSA-N triethylene glycol Chemical compound OCCOCCOCCO ZIBGPFATKBEMQZ-UHFFFAOYSA-N 0.000 description 1
- 229920003169 water-soluble polymer Polymers 0.000 description 1
- 239000001043 yellow dye Substances 0.000 description 1
- 239000002888 zwitterionic surfactant Substances 0.000 description 1
- 239000004711 α-olefin Substances 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
- C11D3/00—Other compounding ingredients of detergent compositions covered in group C11D1/00
- C11D3/16—Organic compounds
- C11D3/20—Organic compounds containing oxygen
- C11D3/2003—Alcohols; Phenols
- C11D3/2006—Monohydric alcohols
- C11D3/201—Monohydric alcohols linear
-
- 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
- C11D17/0008—Detergent materials or soaps characterised by their shape or physical properties aqueous liquid non soap compositions
- C11D17/0017—Multi-phase liquid compositions
-
- 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
- C11D3/00—Other compounding ingredients of detergent compositions covered in group C11D1/00
- C11D3/16—Organic compounds
- C11D3/20—Organic compounds containing oxygen
- C11D3/2003—Alcohols; Phenols
-
- 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
- C11D3/00—Other compounding ingredients of detergent compositions covered in group C11D1/00
- C11D3/16—Organic compounds
- C11D3/20—Organic compounds containing oxygen
- C11D3/2003—Alcohols; Phenols
- C11D3/2006—Monohydric alcohols
- C11D3/2017—Monohydric alcohols branched
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- Chemical & Material Sciences (AREA)
- Oil, Petroleum & Natural Gas (AREA)
- Life Sciences & Earth Sciences (AREA)
- Engineering & Computer Science (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Wood Science & Technology (AREA)
- Organic Chemistry (AREA)
- Emergency Medicine (AREA)
- Health & Medical Sciences (AREA)
- Cosmetics (AREA)
- Medicinal Preparation (AREA)
- Agricultural Chemicals And Associated Chemicals (AREA)
- Detergent Compositions (AREA)
Abstract
Description
Die Erfindung betrifft wässrige Tensidzubereitungen, die im Ruhezustand in Form von zwei oder mehr entmischten, flüssigen, wässrigen Phasen vorliegen, die durch Bewegung zeitweise ineinander dispergierbar sind.The invention relates to aqueous surfactant preparations, which are at rest in the form of two or more segregated, liquid, aqueous phases that are temporarily agitated are dispersible in one another.
Die Verbraucher erwarten bei einem kosmetischen Reinigungs- oder Pflegemittel in der Regel nicht nur eine bestimmte, für den Körper, die Haut, Haare und Zähne nützliche Wirkung, sondern in gleicher Weise auch ein attraktives Aussehen und eine die Wirkung unterstreichende galenische Zubereitung.As a rule, consumers expect cosmetic cleaning or care products not just a specific effect that is beneficial for the body, skin, hair and teeth, but in the same way also an attractive appearance and an effect underlining galenic preparation.
So wird z. B. in DE 16 17 208 A1 ein flüssiges Reinigungsmittel beschrieben, das aus einer nichtwässrigen, öligen Phase und einer wässrigen Phase besteht, die durch Schütteln in eine instabile Öl-in-Wasser-Emulsion überführt werden können. Solche Zubereitungen sind aber nur mit einem hohen Anteil an Ölkomponenten zu realisieren und für viele kosmetische Reinigungszwecke wegen dieses hohen Ölgehalts ungeeignet.So z. B. in DE 16 17 208 A1 describes a liquid cleaning agent which consists of a non-aqueous, oily phase and an aqueous phase, which by shaking in a unstable oil-in-water emulsion can be transferred. But such preparations are only possible with a high proportion of oil components and for many cosmetic ones Cleaning purposes unsuitable because of this high oil content.
In EP 0116 442 A1 wird ein Shampoo beschrieben, das aus zwei entmischten wässrigen Phasen besteht und dessen spezifisch schwerere, untere Phase einen Gehalt von wenigstens 6 Gew.-% gelöstem Natriumhexametaphosphat aufweist. Ein so hoher Gehalt an kondensierten Phosphaten ist aber weder anwendungstechnisch vorteilhaft noch ökologisch erwünscht.EP 0116 442 A1 describes a shampoo that consists of two separated aqueous solutions Phases exists and its specifically heavier, lower phase a content of at least Has 6 wt .-% dissolved sodium hexametaphosphate. Such a high content of condensed However, phosphates are neither advantageous in terms of application technology nor ecologically desirable.
Schließlich waren aus JP 62 263 297 A1 kosmetische Reinigungsmittel bekannt, die zwei entmischte, flüssige, wässrige Phasen aufweisen und die durch einen Gehalt an Tensiden und wasserlöslichen Polymeren gekennzeichnet sind. Die dort beschriebenen Reinigungsmittel benötigen jedoch relativ lang (mehrere Stunden) bis sie sich nach dem Vermischen im Ruhezustand wieder entmischen.Finally, from JP 62 263 297 A1 cosmetic cleaning agents were known, the two have segregated, liquid, aqueous phases and the content of surfactants and water-soluble polymers are marked. The cleaning agents described there however, take a relatively long time (several hours) before they mix in the Separate the idle state again.
Es wurde daher nach Möglichkeiten gesucht, um eine raschere Entmischung der beiden wässrigen Phasen solcher Reinigungsmittel zu erreichen, damit der Verbraucher auch bei häufigerer Verwendung solche Produkte jedesmal im entmischten Zustand vorfindet.Therefore, possibilities were sought to enable the two to separate more quickly to achieve aqueous phases of such cleaning agents, so that the consumer also Frequent use of such products is always found in the segregated state.
Als Lösung dieser Aufgabe wurde gefunden, daß eine Beschleunigung der Entmischung im Ruhezustand durch einen Gehalt an wasserlöslichen, ein- oder mehrwertigen Alkoholen erreicht werden kann.As a solution to this problem, it was found that an acceleration of the segregation in Hibernation due to the content of water-soluble, mono- or polyhydric alcohols can be achieved.
Gegenstand der Erfindung sind daher wässrige, im Ruhezustand in Form von zwei oder mehr entmischten wässrigen, unter Bewegung zeitweise ineinander dispergierbaren Phasen vorliegende Zubereitungen mit wenigstens einer gelösten oberflächenaktiven Verbindung und wenigstens einer gelösten Polymerverbindung, die zur Beschleunigung der Phasentrennung im Ruhezustand wenigstens einen wasserlöslichen, ein- oder mehrwertigen Alkohol mit 2-9 C-Atomen enthalten.The invention therefore relates to aqueous, at rest in the form of two or more segregated aqueous phases that are temporarily dispersible in one another with movement present preparations with at least one dissolved surface-active compound and at least one dissolved polymer compound, which is used to accelerate the phase separation at rest, at least one water-soluble, mono- or polyhydric alcohol with 2-9 Contain carbon atoms.
Die in der erfindungsgemäßen Zubereitung enthaltenen, gelösten oberflächenaktiven Verbindungen können ionogene oder nichtionische Verbindungen sein, entscheidend ist, daß sie eine bevorzugt lineare Lipidgruppe mit 8-22 C-Atomen und wenigstens eine wasserlöslich machende Polyol- oder Polyethergruppe oder eine wasserlöslich machende salzbildende Gruppe, z. B. eine Carboxyl-, Sulfonat- oder Sulfatestergruppe oder beides oder eine ggf. quartäre Ammoniumgruppe oder ampholytische Aminocarboxylat- oder Aminosulfonatgruppe oder eine Betaingruppierung, bevorzugt an einem Ende der linearen Lipidgruppe enthalten.The dissolved surface-active substances contained in the preparation according to the invention Compounds can be ionic or non-ionic compounds, it is crucial that they have a preferably linear lipid group with 8-22 carbon atoms and at least one water-solubilizing polyol or polyether group or a water-solubilizing group salt-forming group, e.g. B. a carboxyl, sulfonate or sulfate ester group or both or an optionally quaternary ammonium group or ampholytic aminocarboxylate or Aminosulfonate group or a betaine grouping, preferably at one end of the linear Contain lipid group.
Als kosmetische Reinigungsmittel eignen sich bevorzugt solche Zubereitungen, die als
oberflächenaktive Verbindungen schaumstarke anionische Tenside, bevorzugt also solche mit
anionischen Sulfonat- oder Sulfatestergruppen in Form ihrer Alkali-, Magnesium- oder
Ammoniumsalze enthalten. Solche bevorzugt geeigneten Tenside sind vor allem die
Alkylpolyglycolether-sulfat-Salze oder die Alkylpolyglycolether-sulfosuccinat-Salze, die z. B.
als Natriumsalze die allgemeine Formel I bzw. II erfüllen:
Suitable cosmetic cleaning agents are preferably those preparations which contain, as surface-active compounds, high-foaming anionic surfactants, preferably those with anionic sulfonate or sulfate ester groups in the form of their alkali metal, magnesium or ammonium salts. Such preferred surfactants are especially the alkyl polyglycol ether sulfate salts or the alkyl polyglycol ether sulfosuccinate salts, which z. B. as sodium salts meet the general formula I or II:
In diesen Formeln ist R1 und R2 eine bevorzugt lineare Alkylgruppe mit 8-22, bevorzugt mit 12-18 C-Atomen und n eine Zahl von 1-6, bevorzugt von 2-4.In these formulas, R 1 and R 2 are a preferably linear alkyl group with 8-22, preferably with 12-18 C atoms and n is a number from 1-6, preferably from 2-4.
Bevorzugt geeignete Zubereitungen enthalten als oberflächenaktive Verbindungen ein Alkylpolyglycolethersulfatsalz oder ein Alkylpolyglycolether-sulfosuccinatsalz mit einer Alkylgruppe mit 12-18 C-Atomen und 1-6 Glycolethergruppen oder ein Gemisch davon in einer Menge von insgesamt 5-20 Gew.-% der Zubereitung, bevorzugt von 8-12 Gew.-% der Zubereitung.Preparations which are preferably suitable contain as surface-active compounds Alkyl polyglycol ether sulfate salt or an alkyl polyglycol ether sulfosuccinate salt with one Alkyl group with 12-18 C atoms and 1-6 glycol ether groups or a mixture thereof in a total amount of 5-20% by weight of the preparation, preferably 8-12% by weight the preparation.
Weitere geeignete anionische Tenside sind z. B. Seifen, N-Acylaminosäure-Salze, Alkylphosphat-Salze, Alkylpolyglycolether-carboxylat-Salze, Alkylsulfat-Alkanolamin-Salze, Alkylsulfonat-Salze, α-Olefinsulfonat-Salze, Acylisethionat-Salze und Acyltaurin-Salze.Other suitable anionic surfactants are e.g. B. soaps, N-acylamino acid salts, Alkyl phosphate salts, alkyl polyglycol ether carboxylate salts, alkyl sulfate alkanolamine salts, Alkyl sulfonate salts, α-olefin sulfonate salts, acyl isethionate salts and acyl taurine salts.
Daneben können auch amphotere und/oder zwitterionische Tenside, z. B. Cocoamphoglycinat oder Cocoamidopropyl-dimethyl-ammonio-glycinat und Betaintenside enthalten sein.In addition, amphoteric and / or zwitterionic surfactants, e.g. B. Cocoamphoglycinate or cocoamidopropyl-dimethyl-ammonio-glycinate and betaine surfactants.
Auch nichtionische Tenside, z. B. die Anlagerungsprodukte von 6-30 Mol Ethylenoxid an Fettsäuren, Fettalkohole, Fettsäuremonoglyceride, Fettsäurealkanolamide, Fettsäure-sorbitan ester, Alkylphenole, Methylglucosid-Fettsäureester und andere polare Lipide sowie Alkylglucoside und deren Ethylenoxidaddukte können als oberflächenaktive Stoffe enthalten sein.Also nonionic surfactants, e.g. B. the addition products of 6-30 moles of ethylene oxide Fatty acids, fatty alcohols, fatty acid monoglycerides, fatty acid alkanolamides, fatty acid sorbitan esters, alkylphenols, methylglucoside fatty acid esters and other polar lipids as well Alkyl glucosides and their ethylene oxide adducts can contain surfactants his.
Die Gesamtmenge an oberflächenaktiven Stoffen kann 5-40 Gew.-% betragen, eine Menge von 5-20 Gew.-% ist aber bevorzugt, da sonst die rasche Entmischung der Phasen nicht mehr gewährleistet ist.The total amount of surfactants can be 5-40% by weight, an amount of 5-20% by weight is preferred, since otherwise the rapid separation of the phases is not more is guaranteed.
Als gelöste Polymerverbindungen eignen sich alle in Wasser oder wässrigen Tensidlösungen bei 20°C in Mengen von wenigstens 1 Gew.-% löslichen natürlichen oder synthetischen hochmolekularen Stoffe mit wiederkehrenden Strukturelementen. Als natürliche Polymere werden dabei wasserlösliche Proteine oder wasserlösliche Polysaccharide oder die wasserlöslichen Derivate von wasserunlöslichen Proteinen oder Polysacchariden verstanden. Suitable polymer compounds are all dissolved in water or aqueous surfactant solutions at 20 ° C in amounts of at least 1% by weight soluble natural or synthetic high molecular substances with recurring structural elements. As natural polymers are water-soluble proteins or water-soluble polysaccharides or the understood water-soluble derivatives of water-insoluble proteins or polysaccharides.
Geeignete natürliche Polymere sind z. B. Albumine, Gelatine, Glycosaminoglycane (Hyaluronsäure), Chitosane, Stärke, Guar, Celluloseether, z. B. Methylcellulosen oder Hydroxyethylcellulosen, Carboxymethylcellulosen und kationische Cellulosederivate, z. B. die mit Epoxypropyl-trimethylammoinumchlorid modifizierten Stärke-, Guar- oder Celluloseether. Auch die wasserlöslichen Biopolymeren wie z. B. Xanthan-Gum oder die Dextrane und Pullulan sind geeignete Polymerverbindungen.Suitable natural polymers are e.g. B. albumins, gelatins, glycosaminoglycans (Hyaluronic acid), chitosans, starch, guar, cellulose ether, e.g. B. methyl celluloses or Hydroxyethyl celluloses, carboxymethyl celluloses and cationic cellulose derivatives, e.g. B. the starch, guar or modified with epoxypropyltrimethylammoinum chloride Cellulose ether. The water-soluble biopolymers such as. B. xanthan gum or Dextrans and pullulan are suitable polymer compounds.
Geeignete synthetische Polymerverbindungen sind z. B. Polyvinylalkohole, Polyvinylpyrrolidon, Polyacrylamide und Polyalkylenglykole mit Molekulargewichten von mehr als 1000 D. Auch wasserlösliche Copolymerisate der Acrylsäure, des Acrylamids, des Vinylpyrrolidons und anderer wasserlöslicher Monomeren mit nicht-wasserlöslichen Comonomeren sind als Polymerverbindungen im Sinne der vorliegenden Erfindung geeignet.Suitable synthetic polymer compounds are e.g. B. polyvinyl alcohols, Polyvinylpyrrolidone, polyacrylamides and polyalkylene glycols with molecular weights of more than 1000 D. Also water-soluble copolymers of acrylic acid, acrylamide, Vinyl pyrrolidones and other water-soluble monomers with non-water-soluble ones Comonomers are suitable as polymer compounds for the purposes of the present invention.
Bevorzugt geeignet zur Herstellung der erfindungsgemäßen Zubereitungen sind Polymerverbindungen ausgewählt aus Polypropylenglycolen mit Molekulargewichten von mehr als 1000 D, Hydroxyethylcellulosen, Xanthan-Gum, Dextran, Natrium-Hyaluronat und kationischen Celluloseethern. Die zur Entmischung erforderlichen Mengen an Polymerverbindungen sind von der Art und dem Molekulargewicht der Polymerverbindung abhängig, dabei gilt allgemein, daß die erforderlichen Mengen um so niedriger sind, je höher das Molekulargewicht der Polymerverbindung ist. Von den sehr hochmolekularen Salzen der Hyaluronsäure oder von Xanthan-Gum sind daher Mengen von 0,1-1 Gew.-%, von Celluloseethern wie z. B. Hydroxyethylcellulose oder den kationischen Celluloseethern sind Mengen von 0,5-6 Gew.-% ausreichend, während z. B. Polypropylenglycole oder abgebaute Dextrane in Mengen von 2-20 Gew.-% enthalten sein sollen. Die Obergrenze des Gehalts an Polymerverbindungen ist so zu wählen, daß die Zubereitung nicht geliert und die Entmischung durch die Zähigkeit der Phasen nicht behindert wird.Are preferably suitable for the preparation of the preparations according to the invention Polymer compounds selected from polypropylene glycols with molecular weights of more than 1000 D, hydroxyethyl celluloses, xanthan gum, dextran, sodium hyaluronate and cationic cellulose ethers. The quantities required for segregation Polymer compounds are of the type and molecular weight of the polymer compound dependent, the general rule being that the quantities required are lower, the higher is the molecular weight of the polymer compound. Of the very high molecular salts of Hyaluronic acid or xanthan gum are therefore amounts of 0.1-1% by weight Cellulose ethers such as B. are hydroxyethyl cellulose or the cationic cellulose ethers Amounts of 0.5-6 wt .-% sufficient, for. B. polypropylene glycols or degraded Dextrans should be contained in amounts of 2-20% by weight. The upper limit of the salary Polymer compounds should be selected so that the preparation does not gel and the Separation is not hindered by the toughness of the phases.
Die gelösten oberflächenaktiven Verbindungen und Polymerverbindungen können einzeln oder als Kombinationen von zwei oder mehr solcher Tenside oder Polymeren in den Zubereitungen enthalten sein. Dabei hat sich gezeigt, daß es für die Entmischung der Zusammensetzung vorteilhaft ist, wenn wenigstens zwei unterschiedliche oberflächenaktive Verbindungen oder wenigstens zwei unterschiedliche Polymerverbindungen in den erfindungsgemäßen Zusammensetzungen enthalten sind. Bei den Polymerverbindungen hat sich dabei eine Kombination eines besonders hochmolekularen Polymerisats mit einer niedrigmolekularen Polymerverbindung als besonders geeignet erwiesen. So haben sich z. B. Kombinationen von Natrium-Hyaluronat mit Cellulosederivaten oder von Polypropylenglycolen mit mittlerem Molekulargewichten von 2000 D und mehr mit solchen von 1000 D und weniger besonders gut bewährt.The dissolved surface-active compounds and polymer compounds can be used individually or as combinations of two or more such surfactants or polymers in the Preparations may be included. It has been shown that it is for the segregation of the Composition is advantageous if at least two different surfactants Compounds or at least two different polymer compounds in the compositions according to the invention are included. With the polymer compounds a combination of a particularly high molecular weight polymer with a low molecular weight polymer compound proved to be particularly suitable. So z. B. Combinations of sodium hyaluronate with cellulose derivatives or of Polypropylene glycols with average molecular weights of 2000 D and more with such of 1000 D and less, especially well proven.
Als wasserlösliche ein- oder mehrwertige Alkohole eignen sich alle aliphatischen Alkohole, Diole oder Polyole, bevorzugt solche mit 2-9 Kohlenstoffatomen, die in Mengen von wenigstens 1 Gew.-% in Wasser bei 20°C klar löslich sind. Solche ein- oder mehrwertigen Alkohole sind in einer Menge von 1-40 Gew.-% in den erfindungsgemäßen Zubereitungen enthalten. Geeignete Alkohole sind z. B. Ethanol, 1-Propanol, 2-Propanol (Isopropanol), n- Butanol, Isobutanol, Methoxyethanol oder 2-Ethoxyethanol. Geeignete Diole sind z. B. Ethylenglycol, 1,2-Propylenglycol, 1,4-Butandiol, 1,5-Pentandiol, 1,6-Hexandiol, Diethylenglycol, Triethylenglycol, Dipropylenglycol, Glycerinmonomethylether oder Cyclohexandiol. Geeignete Polyole sind Glycerin, Erythrit, Diglycerin, Triglycerin, Sorbit, Methylglucosid, Butylglucosid, Pentaerythrit oder Trimethyl-propan.Suitable water-soluble monohydric or polyhydric alcohols are all aliphatic alcohols, Diols or polyols, preferably those with 2-9 carbon atoms, in amounts of at least 1% by weight are clearly soluble in water at 20 ° C. Such mono- or multi-valued Alcohols are in an amount of 1-40% by weight in the preparations according to the invention contain. Suitable alcohols are e.g. B. ethanol, 1-propanol, 2-propanol (isopropanol), n- Butanol, isobutanol, methoxyethanol or 2-ethoxyethanol. Suitable diols are e.g. B. Ethylene glycol, 1,2-propylene glycol, 1,4-butanediol, 1,5-pentanediol, 1,6-hexanediol, Diethylene glycol, triethylene glycol, dipropylene glycol, glycerol monomethyl ether or Cyclohexanediol. Suitable polyols are glycerol, erythritol, diglycerol, triglycerol, sorbitol, Methyl glucoside, butyl glucoside, pentaerythritol or trimethyl propane.
Die erfindungsgemäßen Mehrphasen-Zubereitungen der vorliegenden Erfindung entmischen sich besonders leicht, wenn als Alkohol Ethanol oder Isopropanol in einer Menge von 2-20 Gew.-% enthalten ist. Es konnten auf diese Weise Zubereitungen erhalten werden, die nach intensiver Vermischung der Phasen im Ruhezustand innerhalb von weniger als 10 Minuten sich vollständig entmischen und in Form von getrennten, klaren Phasen vorliegen.The multiphase preparations according to the invention of the present invention separate is particularly easy when alcohol or ethanol in an amount of 2-20 wt .-% is included. In this way it was possible to obtain preparations which after intensive mixing of the phases at rest within less than 10 minutes separate completely and are in the form of separate, clear phases.
Die Separation diskreter wässriger Phasen kann weiterhin durch einen Gehalt an gelösten Elektrolytsalzen gefördert werden. Geeignete Elektrolytsalze sind vor allem wasserlösliche anorganische Salze, z. B. Alkalihalogenide wie Kochsalz (Natriumchlorid), Calzium- oder Magnesium-chlorid, die Sulfate der Alkalimetalle oder des Magnesiums, Natriumbicarbonat, Natriumhydrogenphosphat und Natriumpyrophosphat. Geeignet sind aber auch die Salze von organischen, niedermolekularen Säuren, z. B. Natriumacetat, Natriumcitrat, Natriumlactat, Natrium-toluolsulfonat, Natrium-xylolsulfonat oder Natriumbenzoat. Bevorzugt sind wasserlösliche, anorganische Elektrolytsalze in eine Menge von 1-6 Gew.-% enthalten.The separation of discrete aqueous phases can also be due to a content of dissolved Electrolyte salts are promoted. Suitable electrolyte salts are above all water-soluble inorganic salts, e.g. B. alkali halides such as common salt (sodium chloride), calcium or Magnesium chloride, the sulfates of alkali metals or magnesium, sodium bicarbonate, Sodium hydrogen phosphate and sodium pyrophosphate. However, the salts of organic, low molecular weight acids, e.g. B. sodium acetate, sodium citrate, sodium lactate, Sodium toluenesulfonate, sodium xylene sulfonate or sodium benzoate. Are preferred Contain water-soluble, inorganic electrolyte salts in an amount of 1-6 wt .-%.
Neben den genannten Komponenten können die erfindungsgemäßen Mehrphasen- Zubereitungen auch weitere, für die Anwendung oder das Aussehen vorteilhafte Komponenten enthalten, wie sie in kosmetischen Reinigungs- und Pflegemitteln üblich sind. Dies sind z. B. Farbstoffe, Duftstoffe, Konservierungsmittel und PH-Stellmittel (Pfuffersalze), Komplexbildner, Antioxidantien und kosmetische oder dermatologische Wirksubstanzen, die der Haut ein angenehmes Hautgefühl oder den Haaren eine gute Avivage verleihen oder die spezifischen dermatologischen Effekte auf der Haut bewirken.In addition to the components mentioned, the multiphase Preparations also other advantageous for the application or the appearance Contain components as are common in cosmetic cleaning and care products. These are e.g. B. dyes, fragrances, preservatives and pH adjusting agents (buffer salts), Complexing agents, antioxidants and cosmetic or dermatological active substances that give the skin a pleasant feeling on the skin or give the hair a good finish or the cause specific dermatological effects on the skin.
Von besonderer Bedeutung ist der Zusatz von ein oder zwei Farbstoffen, bevorzugt von solchen, die in den entmischten, wässrigen Phasen eine unterschiedliche Löslichkeit aufweisen und auf diese Weise den Zubereitungen ein besonders ansprechendes Aussehen verleihen. So konnte z. B. durch Zusatz von gelben Farbstoffen wie z. B. Chinolingelb Lack (Lebensmittelfarbstoff E 104), roten Farbstoffen wie Cochenillerot Lack (Lebensmittelfarb stoff E 124) oder blauen Farbstoffen (Sudanblau) unterschiedlich gefärbte Phasen der erfindungsgemäßen Zusammensetzungen erzielt werden.Of particular importance is the addition of one or two dyes, preferably from those that have a different solubility in the segregated, aqueous phases have and in this way the preparations have a particularly attractive appearance to lend. So z. B. by adding yellow dyes such. B. quinoline yellow lacquer (Food coloring E 104), red coloring like Cochenillerot Lack (food coloring fabric E 124) or blue dyes (Sudan blue) differently colored phases of the compositions according to the invention can be achieved.
Die erfindungsgemäßen Tensidzubereitungen können z. B. als Shampoos zur Haarwäsche, als Duschpräparate, Badezusätze, flüssige Seifen - aber auch als flüssige Reinigungsmittel im Haushalt oder als Feinwaschmittel verwendet werden. Das entmischte zwei- oder mehrphasige Erscheinungsbild kann dazu benutzt werden, dem Verbraucher die Zusammensetzung aus reinigenden und pflegenden Komponenten anschaulich zu machen und ihn zu motivieren, das Produkt vor Gebrauch durch Schütteln zu homogenisieren, um von allen Komponenten in gleicher Weise Gebrauch zu machen.The surfactant preparations according to the invention can, for. B. as shampoos for shampooing, as Shower preparations, bath additives, liquid soaps - but also as a liquid cleaning agent in the Household or as a mild detergent. That segregated two or multi-phase appearance can be used to give the consumer the To make the composition of cleaning and care components clear and to motivate him to homogenize the product by shaking before use to use all components in the same way.
Die folgenden Beispiele sollen den Gegenstand der Erfindung näher erläutern - ohne ihn darauf zu beschränken:The following examples are intended to explain the subject matter of the invention in more detail - without it limit to:
Es wurden Zweiphasen-Zusammensetzungen durch Vermischen der in Tabelle I angegebenen Komponenten hergestellt.Two-phase compositions were made by mixing those given in Table I. Components manufactured.
Teilweise wurden auch Farbstoffe eingearbeitet.In some cases, dyes were also incorporated.
Dabei wurde ein Teil des Tensids mit dem Farbstoff gemischt und dann zugegeben. So wurde z. B. in Beispiel 11 ein Teil des wässrigen Ethersulfats mit Sudanblau und ein anderer Teil des Ethersulfats mit Chinolingelblack gefärbt. Auf diese Weise werden - nach Separation der Phasen - eine obere blaue und eine untere gelbe Phase erhalten.Part of the surfactant was mixed with the dye and then added. So it was e.g. B. in Example 11, part of the aqueous ether sulfate with Sudan blue and another part of Colored ether sulfate with quinoline yellow black. In this way - after separation of the Phases - get an upper blue and a lower yellow phase.
Die Phasenseparation erfolgte in einer Zeitspanne von 5-60 Minuten. Die Beispiele mit
einem Gehalt an Ethanol zeigten eine raschere Phasentrennung, meist innerhalb von
10 Minuten.
The phase separation took place over a period of 5-60 minutes. The examples containing ethanol showed a faster phase separation, usually within 10 minutes.
Die in der Tabelle angegebenen Prozentzahlen beziehen sich auf Gewichts-% wasserfreier Aktivsubstanz.The percentages given in the table refer to% by weight anhydrous Active substance.
Es wurden die folgenden Rohstoffe eingesetzt:
LES-Na: Natrium C12/C14-Alkylpoly(2)glycolethersulfat
(Texapon®NSO, Henkel KGaA),
SBE-Na: Sulfobernsteinsäure - Alkyl(C12/14-poly(3)glycolether
monoester-di-Natriumsalz,
(Texapon®SB3, Henkel KGaA),
HEC: Hydroxyethylcellulose,
Viskosität 25°C (1 Gew.-%): 350 m Pa.s,
Substitutionsgrad 2,5,
Natrasol® 250 HR (Hercules),
Xanthan-Gum: Keltrol® SF (Kelco),
IR 400: Polyquaternium-10 (Polymer IR 400, Amerchol),
Dextran: Fa. Sigma, MG: 2-82000,
PPG 600: Polypropylenglycol, Molgewicht ca. 6000.The following raw materials were used:
LES-Na: sodium C 12 / C 14 alkyl poly (2) glycol ether sulfate (Texapon®NSO, Henkel KGaA),
SBE-Na: sulfosuccinic acid - alkyl (C 12/14 -poly (3) glycol ether monoester-di-sodium salt, (Texapon®SB3, Henkel KGaA),
HEC: hydroxyethyl cellulose, viscosity 25 ° C (1% by weight): 350 m Pa.s, degree of substitution 2.5, Natrasol® 250 HR (Hercules),
Xanthan gum: Keltrol® SF (Kelco),
IR 400: Polyquaternium-10 (Polymer IR 400, Amerchol),
Dextran: Sigma, MG: 2-82000,
PPG 600: polypropylene glycol, molecular weight approx. 6000.
Claims (7)
Priority Applications (6)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| DE19915837A DE19915837A1 (en) | 1999-04-08 | 1999-04-08 | Aqueous multiphase surfactant preparations |
| PCT/EP2000/002806 WO2000061716A1 (en) | 1999-04-08 | 2000-03-30 | Aqueous multiphase surfactant preparations |
| EP00920627A EP1165743B1 (en) | 1999-04-08 | 2000-03-30 | Aqueous multiphase surfactant preparations |
| AU41136/00A AU4113600A (en) | 1999-04-08 | 2000-03-30 | Aqueous multiphase surfactant preparations |
| AT00920627T ATE286966T1 (en) | 1999-04-08 | 2000-03-30 | AQUEOUS MULTI-PHASE SURFACTANT PREPARATIONS |
| DE50009223T DE50009223D1 (en) | 1999-04-08 | 2000-03-30 | AQUEOUS MULTI PHASE TENSIDE PREPARATIONS |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| DE19915837A DE19915837A1 (en) | 1999-04-08 | 1999-04-08 | Aqueous multiphase surfactant preparations |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| DE19915837A1 true DE19915837A1 (en) | 2000-10-12 |
Family
ID=7903882
Family Applications (2)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| DE19915837A Withdrawn DE19915837A1 (en) | 1999-04-08 | 1999-04-08 | Aqueous multiphase surfactant preparations |
| DE50009223T Expired - Lifetime DE50009223D1 (en) | 1999-04-08 | 2000-03-30 | AQUEOUS MULTI PHASE TENSIDE PREPARATIONS |
Family Applications After (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| DE50009223T Expired - Lifetime DE50009223D1 (en) | 1999-04-08 | 2000-03-30 | AQUEOUS MULTI PHASE TENSIDE PREPARATIONS |
Country Status (5)
| Country | Link |
|---|---|
| EP (1) | EP1165743B1 (en) |
| AT (1) | ATE286966T1 (en) |
| AU (1) | AU4113600A (en) |
| DE (2) | DE19915837A1 (en) |
| WO (1) | WO2000061716A1 (en) |
Cited By (10)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| WO2001030951A1 (en) * | 1999-10-22 | 2001-05-03 | Reckitt Benckiser France | Compositions and their use |
| DE10206795A1 (en) * | 2002-02-19 | 2003-08-28 | Beiersdorf Ag | Two-phase cosmetic or dermatological compositions useful as sunscreen, artificial tanning or insect repellent products comprise a microemulsion phase and a lipophilic phase |
| FR2871373A1 (en) * | 2004-06-11 | 2005-12-16 | Oreal | METHOD FOR WASHING FROZEN OR CREPUS HAIR |
| WO2006050788A1 (en) * | 2004-11-10 | 2006-05-18 | The Procter & Gamble Company | Clear, two-phase, foam-forming aerosol hairstyling product |
| WO2006069612A3 (en) * | 2004-12-28 | 2006-11-30 | Unilever Plc | Biphasic inducing agent for aqueous cleansing compositions |
| DE102005051860A1 (en) * | 2005-10-25 | 2007-04-26 | Beiersdorf Ag | Aqueous cosmetic preparation, useful as e.g. soaking medium for patch or cloth, comprises 1,2-hexanediol |
| DE102005051864A1 (en) * | 2005-10-25 | 2007-04-26 | Beiersdorf Ag | Cosmetic oil-in-water emulsion for, e.g. ointment, cream, or low-viscosity lotion, includes 1,2-hexanediol, and oil-in-water emulsifiers |
| EP1894994A1 (en) | 2006-08-31 | 2008-03-05 | Henkel KGaA | Two or more phase face cleansing agent with improved reversible mixing and demixing solution |
| DE102014205475A1 (en) * | 2014-03-25 | 2015-10-01 | Beiersdorf Ag | Polypropylene glycols with antimicrobial activity in cosmetic or dermatological preparations |
| WO2019108198A1 (en) * | 2017-11-30 | 2019-06-06 | Colgate-Palmolive Company | Cleansing compositions and use thereof |
Families Citing this family (8)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| DE19951635A1 (en) * | 1999-10-26 | 2001-05-17 | Henkel Kgaa | Aqueous multiphase detergent |
| US6429177B1 (en) * | 2000-08-22 | 2002-08-06 | Unilever Home & Personal Care Usa, Division Of Conopco, Inc. | Separating multi-phase personal wash composition in a transparent or translucent package |
| DE10062045A1 (en) * | 2000-12-13 | 2002-06-27 | Henkel Kgaa | Different colored aqueous multiphase cleaner |
| US6787511B2 (en) * | 2002-08-14 | 2004-09-07 | Unilever Home & Personal Care Usa Division Of Conopco, Inc. | Biphasic composition induced by polydextrose |
| US6727209B2 (en) * | 2002-08-14 | 2004-04-27 | Unilever Home & Personal Care, Usa, Division Of Conopco, Inc. | Biphasic composition induced by polydextrose and sucrose |
| WO2005023975A1 (en) * | 2003-09-03 | 2005-03-17 | Henkel Kommanditgesellschaft Auf Aktien | Multi-phase cosmetic agent for cleansing hair and skin |
| DE10341024A1 (en) * | 2003-09-03 | 2005-03-31 | Hans Schwarzkopf & Henkel Gmbh & Co. Kg | Multiphase surfactant product |
| FR2859626B1 (en) * | 2003-09-12 | 2006-01-27 | Oreal | BIPHASE COMPOSITION AND USES IN THE COSMETIC FIELD |
Family Cites Families (4)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| FR1188460A (en) * | 1955-09-06 | 1959-09-23 | Colgate Palmolive Co | Detergent composition in the form of a suspension |
| GB8421196D0 (en) * | 1984-08-21 | 1984-09-26 | Reckitt & Colmann Prod Ltd | Cleansing compositions |
| JPS62263297A (en) * | 1986-05-09 | 1987-11-16 | ライオン株式会社 | Two-phase separation type liquid cleaning composition |
| DE19811386A1 (en) * | 1998-03-16 | 1999-09-23 | Henkel Kgaa | Aqueous multiphase detergent forming temporary emulsion on shaking and used on hard surfaces |
-
1999
- 1999-04-08 DE DE19915837A patent/DE19915837A1/en not_active Withdrawn
-
2000
- 2000-03-30 DE DE50009223T patent/DE50009223D1/en not_active Expired - Lifetime
- 2000-03-30 EP EP00920627A patent/EP1165743B1/en not_active Expired - Lifetime
- 2000-03-30 AT AT00920627T patent/ATE286966T1/en active
- 2000-03-30 AU AU41136/00A patent/AU4113600A/en not_active Abandoned
- 2000-03-30 WO PCT/EP2000/002806 patent/WO2000061716A1/en not_active Ceased
Cited By (16)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| WO2001030951A1 (en) * | 1999-10-22 | 2001-05-03 | Reckitt Benckiser France | Compositions and their use |
| DE10206795A1 (en) * | 2002-02-19 | 2003-08-28 | Beiersdorf Ag | Two-phase cosmetic or dermatological compositions useful as sunscreen, artificial tanning or insect repellent products comprise a microemulsion phase and a lipophilic phase |
| FR2871373A1 (en) * | 2004-06-11 | 2005-12-16 | Oreal | METHOD FOR WASHING FROZEN OR CREPUS HAIR |
| EP1604641A3 (en) * | 2004-06-11 | 2006-01-25 | L'oreal | Process for cleaning frizzy hair |
| WO2006050788A1 (en) * | 2004-11-10 | 2006-05-18 | The Procter & Gamble Company | Clear, two-phase, foam-forming aerosol hairstyling product |
| WO2006069612A3 (en) * | 2004-12-28 | 2006-11-30 | Unilever Plc | Biphasic inducing agent for aqueous cleansing compositions |
| US8084507B2 (en) | 2005-10-25 | 2011-12-27 | Beiersdorf Ag | Cosmetic O/W emulsion comprising 1,2-hexanediol |
| DE102005051860A1 (en) * | 2005-10-25 | 2007-04-26 | Beiersdorf Ag | Aqueous cosmetic preparation, useful as e.g. soaking medium for patch or cloth, comprises 1,2-hexanediol |
| DE102005051864A1 (en) * | 2005-10-25 | 2007-04-26 | Beiersdorf Ag | Cosmetic oil-in-water emulsion for, e.g. ointment, cream, or low-viscosity lotion, includes 1,2-hexanediol, and oil-in-water emulsifiers |
| EP1894994A1 (en) | 2006-08-31 | 2008-03-05 | Henkel KGaA | Two or more phase face cleansing agent with improved reversible mixing and demixing solution |
| DE102014205475A1 (en) * | 2014-03-25 | 2015-10-01 | Beiersdorf Ag | Polypropylene glycols with antimicrobial activity in cosmetic or dermatological preparations |
| WO2019108198A1 (en) * | 2017-11-30 | 2019-06-06 | Colgate-Palmolive Company | Cleansing compositions and use thereof |
| CN111328341A (en) * | 2017-11-30 | 2020-06-23 | 高露洁-棕榄公司 | Cleaning composition and use thereof |
| AU2017441060B2 (en) * | 2017-11-30 | 2021-04-15 | Colgate-Palmolive Company | Cleansing compositions and use thereof |
| CN111328341B (en) * | 2017-11-30 | 2021-12-17 | 高露洁-棕榄公司 | Cleaning composition and use thereof |
| US11459527B2 (en) | 2017-11-30 | 2022-10-04 | Colgate-Palmolive Company | Cleansing compositions and use thereof |
Also Published As
| Publication number | Publication date |
|---|---|
| WO2000061716A1 (en) | 2000-10-19 |
| EP1165743B1 (en) | 2005-01-12 |
| DE50009223D1 (en) | 2005-02-17 |
| EP1165743A1 (en) | 2002-01-02 |
| ATE286966T1 (en) | 2005-01-15 |
| AU4113600A (en) | 2000-11-14 |
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| 8130 | Withdrawal |