EP1126019B1 - Use of an aqueous multiphase cleaning agent for cleaning hard surfaces - Google Patents
Use of an aqueous multiphase cleaning agent for cleaning hard surfaces Download PDFInfo
- Publication number
- EP1126019B1 EP1126019B1 EP01103811A EP01103811A EP1126019B1 EP 1126019 B1 EP1126019 B1 EP 1126019B1 EP 01103811 A EP01103811 A EP 01103811A EP 01103811 A EP01103811 A EP 01103811A EP 1126019 B1 EP1126019 B1 EP 1126019B1
- Authority
- EP
- European Patent Office
- Prior art keywords
- phase
- composition according
- alkyl
- composition
- mixtures
- 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.)
- Revoked
Links
- 238000004140 cleaning Methods 0.000 title claims description 10
- 239000012459 cleaning agent Substances 0.000 title description 12
- 239000012071 phase Substances 0.000 claims abstract description 67
- 239000004094 surface-active agent Substances 0.000 claims abstract description 16
- 239000000839 emulsion Substances 0.000 claims abstract description 15
- 239000008346 aqueous phase Substances 0.000 claims abstract description 9
- 239000007788 liquid Substances 0.000 claims abstract description 7
- 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 claims abstract description 6
- 235000019982 sodium hexametaphosphate Nutrition 0.000 claims abstract description 6
- 239000001577 tetrasodium phosphonato phosphate Substances 0.000 claims abstract description 6
- 239000000203 mixture Substances 0.000 claims description 63
- 230000002209 hydrophobic effect Effects 0.000 claims description 14
- -1 alkali metal gluconates Chemical class 0.000 claims description 13
- 150000002170 ethers Chemical class 0.000 claims description 13
- 239000002736 nonionic surfactant Substances 0.000 claims description 11
- 229920000151 polyglycol Polymers 0.000 claims description 11
- 239000010695 polyglycol Substances 0.000 claims description 11
- 125000000217 alkyl group Chemical group 0.000 claims description 8
- 239000003945 anionic surfactant Substances 0.000 claims description 8
- 238000005191 phase separation Methods 0.000 claims description 8
- 238000009835 boiling Methods 0.000 claims description 7
- 150000001340 alkali metals Chemical class 0.000 claims description 6
- 150000001983 dialkylethers Chemical class 0.000 claims description 6
- 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 description 5
- 239000003093 cationic surfactant Substances 0.000 claims description 5
- 229930195733 hydrocarbon Natural products 0.000 claims description 5
- 150000002430 hydrocarbons Chemical class 0.000 claims description 5
- FAPWRFPIFSIZLT-UHFFFAOYSA-M sodium chloride Inorganic materials [Na+].[Cl-] FAPWRFPIFSIZLT-UHFFFAOYSA-M 0.000 claims description 5
- 239000000341 volatile oil Substances 0.000 claims description 5
- NKJOXAZJBOMXID-UHFFFAOYSA-N 1,1'-Oxybisoctane Chemical class CCCCCCCCOCCCCCCCC NKJOXAZJBOMXID-UHFFFAOYSA-N 0.000 claims description 4
- QGZKDVFQNNGYKY-UHFFFAOYSA-N Ammonia Chemical compound N QGZKDVFQNNGYKY-UHFFFAOYSA-N 0.000 claims description 4
- NLXLAEXVIDQMFP-UHFFFAOYSA-N Ammonia chloride Chemical compound [NH4+].[Cl-] NLXLAEXVIDQMFP-UHFFFAOYSA-N 0.000 claims description 4
- WCUXLLCKKVVCTQ-UHFFFAOYSA-M Potassium chloride Chemical compound [Cl-].[K+] WCUXLLCKKVVCTQ-UHFFFAOYSA-M 0.000 claims description 4
- QAOWNCQODCNURD-UHFFFAOYSA-L Sulfate Chemical compound [O-]S([O-])(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-L 0.000 claims description 4
- 229910052783 alkali metal Inorganic materials 0.000 claims description 4
- 125000000129 anionic group Chemical group 0.000 claims description 4
- XMGQYMWWDOXHJM-UHFFFAOYSA-N limonene Chemical compound CC(=C)C1CCC(C)=CC1 XMGQYMWWDOXHJM-UHFFFAOYSA-N 0.000 claims description 4
- HZAXFHJVJLSVMW-UHFFFAOYSA-N 2-Aminoethan-1-ol Chemical compound NCCO HZAXFHJVJLSVMW-UHFFFAOYSA-N 0.000 claims description 3
- BVKZGUZCCUSVTD-UHFFFAOYSA-M Bicarbonate Chemical class OC([O-])=O BVKZGUZCCUSVTD-UHFFFAOYSA-M 0.000 claims description 3
- 150000001860 citric acid derivatives Chemical class 0.000 claims description 3
- 239000002270 dispersing agent Substances 0.000 claims description 3
- MGFYIUFZLHCRTH-UHFFFAOYSA-N nitrilotriacetic acid Chemical class OC(=O)CN(CC(O)=O)CC(O)=O MGFYIUFZLHCRTH-UHFFFAOYSA-N 0.000 claims description 3
- 235000015424 sodium Nutrition 0.000 claims description 3
- 239000011780 sodium chloride Substances 0.000 claims description 3
- GSEJCLTVZPLZKY-UHFFFAOYSA-N Triethanolamine Chemical compound OCCN(CCO)CCO GSEJCLTVZPLZKY-UHFFFAOYSA-N 0.000 claims description 2
- 229910001514 alkali metal chloride Inorganic materials 0.000 claims description 2
- 229910000272 alkali metal oxide Inorganic materials 0.000 claims description 2
- 229910001617 alkaline earth metal chloride Inorganic materials 0.000 claims description 2
- 229910001860 alkaline earth metal hydroxide Inorganic materials 0.000 claims description 2
- 150000001412 amines Chemical class 0.000 claims description 2
- 229910021529 ammonia Inorganic materials 0.000 claims description 2
- 235000019270 ammonium chloride Nutrition 0.000 claims description 2
- 235000011130 ammonium sulphate Nutrition 0.000 claims description 2
- 150000004649 carbonic acid derivatives Chemical class 0.000 claims description 2
- 229940087305 limonene Drugs 0.000 claims description 2
- 235000001510 limonene Nutrition 0.000 claims description 2
- 239000010665 pine oil Substances 0.000 claims description 2
- 239000001103 potassium chloride Substances 0.000 claims description 2
- 235000011164 potassium chloride Nutrition 0.000 claims description 2
- 235000011151 potassium sulphates Nutrition 0.000 claims description 2
- 150000003467 sulfuric acid derivatives Chemical class 0.000 claims description 2
- 229910021653 sulphate ion Inorganic materials 0.000 claims 2
- 239000001166 ammonium sulphate Substances 0.000 claims 1
- 239000003599 detergent Substances 0.000 abstract description 7
- 239000003795 chemical substances by application Substances 0.000 description 37
- RTZKZFJDLAIYFH-UHFFFAOYSA-N Diethyl ether Chemical compound CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 description 11
- 125000004432 carbon atom Chemical group C* 0.000 description 10
- HEMHJVSKTPXQMS-UHFFFAOYSA-M sodium hydroxide Inorganic materials [OH-].[Na+] HEMHJVSKTPXQMS-UHFFFAOYSA-M 0.000 description 9
- 125000005233 alkylalcohol group Chemical group 0.000 description 7
- 150000002191 fatty alcohols Chemical class 0.000 description 6
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 5
- 150000003839 salts Chemical class 0.000 description 5
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 5
- 239000002280 amphoteric surfactant Substances 0.000 description 4
- 150000001875 compounds Chemical class 0.000 description 4
- 239000004033 plastic Substances 0.000 description 4
- 229920003023 plastic Polymers 0.000 description 4
- WBIQQQGBSDOWNP-UHFFFAOYSA-N 2-dodecylbenzenesulfonic acid Chemical compound CCCCCCCCCCCCC1=CC=CC=C1S(O)(=O)=O WBIQQQGBSDOWNP-UHFFFAOYSA-N 0.000 description 3
- KWYUFKZDYYNOTN-UHFFFAOYSA-M Potassium hydroxide Chemical compound [OH-].[K+] KWYUFKZDYYNOTN-UHFFFAOYSA-M 0.000 description 3
- 239000000654 additive Substances 0.000 description 3
- 150000001338 aliphatic hydrocarbons Chemical class 0.000 description 3
- KRKNYBCHXYNGOX-UHFFFAOYSA-N citric acid Chemical compound OC(=O)CC(O)(C(O)=O)CC(O)=O KRKNYBCHXYNGOX-UHFFFAOYSA-N 0.000 description 3
- 235000014113 dietary fatty acids Nutrition 0.000 description 3
- 239000000194 fatty acid Substances 0.000 description 3
- 229930195729 fatty acid Natural products 0.000 description 3
- 150000004665 fatty acids Chemical class 0.000 description 3
- 229930182470 glycoside Natural products 0.000 description 3
- 238000000034 method Methods 0.000 description 3
- 238000006384 oligomerization reaction Methods 0.000 description 3
- 239000002304 perfume Substances 0.000 description 3
- KDYFGRWQOYBRFD-UHFFFAOYSA-N succinic acid Chemical compound OC(=O)CCC(O)=O KDYFGRWQOYBRFD-UHFFFAOYSA-N 0.000 description 3
- KBPLFHHGFOOTCA-UHFFFAOYSA-N 1-Octanol Chemical compound CCCCCCCCO KBPLFHHGFOOTCA-UHFFFAOYSA-N 0.000 description 2
- WNWHHMBRJJOGFJ-UHFFFAOYSA-N 16-methylheptadecan-1-ol Chemical compound CC(C)CCCCCCCCCCCCCCCO WNWHHMBRJJOGFJ-UHFFFAOYSA-N 0.000 description 2
- AEQDJSLRWYMAQI-UHFFFAOYSA-N 2,3,9,10-tetramethoxy-6,8,13,13a-tetrahydro-5H-isoquinolino[2,1-b]isoquinoline Chemical compound C1CN2CC(C(=C(OC)C=C3)OC)=C3CC2C2=C1C=C(OC)C(OC)=C2 AEQDJSLRWYMAQI-UHFFFAOYSA-N 0.000 description 2
- SRBFZHDQGSBBOR-IOVATXLUSA-N D-xylopyranose Chemical compound O[C@@H]1COC(O)[C@H](O)[C@H]1O SRBFZHDQGSBBOR-IOVATXLUSA-N 0.000 description 2
- KFZMGEQAYNKOFK-UHFFFAOYSA-N Isopropanol Chemical compound CC(C)O KFZMGEQAYNKOFK-UHFFFAOYSA-N 0.000 description 2
- CDBYLPFSWZWCQE-UHFFFAOYSA-L Sodium Carbonate Chemical compound [Na+].[Na+].[O-]C([O-])=O CDBYLPFSWZWCQE-UHFFFAOYSA-L 0.000 description 2
- XSQUKJJJFZCRTK-UHFFFAOYSA-N Urea Chemical compound NC(N)=O XSQUKJJJFZCRTK-UHFFFAOYSA-N 0.000 description 2
- 239000002253 acid Substances 0.000 description 2
- WNLRTRBMVRJNCN-UHFFFAOYSA-N adipic acid Chemical compound OC(=O)CCCCC(O)=O WNLRTRBMVRJNCN-UHFFFAOYSA-N 0.000 description 2
- 150000001298 alcohols Chemical class 0.000 description 2
- 150000008051 alkyl sulfates Chemical class 0.000 description 2
- 125000000484 butyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 description 2
- NOPFSRXAKWQILS-UHFFFAOYSA-N docosan-1-ol Chemical compound CCCCCCCCCCCCCCCCCCCCCCO NOPFSRXAKWQILS-UHFFFAOYSA-N 0.000 description 2
- POULHZVOKOAJMA-UHFFFAOYSA-N dodecanoic acid Chemical compound CCCCCCCCCCCC(O)=O POULHZVOKOAJMA-UHFFFAOYSA-N 0.000 description 2
- 229940060296 dodecylbenzenesulfonic acid Drugs 0.000 description 2
- 239000000975 dye Substances 0.000 description 2
- 239000003792 electrolyte Substances 0.000 description 2
- 239000003205 fragrance Substances 0.000 description 2
- 150000004676 glycans Chemical class 0.000 description 2
- 125000005842 heteroatom Chemical group 0.000 description 2
- BXWNKGSJHAJOGX-UHFFFAOYSA-N hexadecan-1-ol Chemical compound CCCCCCCCCCCCCCCCO BXWNKGSJHAJOGX-UHFFFAOYSA-N 0.000 description 2
- 238000005984 hydrogenation reaction Methods 0.000 description 2
- 239000003752 hydrotrope Substances 0.000 description 2
- BTFJIXJJCSYFAL-UHFFFAOYSA-N icosan-1-ol Chemical compound CCCCCCCCCCCCCCCCCCCCO BTFJIXJJCSYFAL-UHFFFAOYSA-N 0.000 description 2
- YDSWCNNOKPMOTP-UHFFFAOYSA-N mellitic acid Chemical compound OC(=O)C1=C(C(O)=O)C(C(O)=O)=C(C(O)=O)C(C(O)=O)=C1C(O)=O YDSWCNNOKPMOTP-UHFFFAOYSA-N 0.000 description 2
- QJGQUHMNIGDVPM-UHFFFAOYSA-N nitrogen group Chemical group [N] QJGQUHMNIGDVPM-UHFFFAOYSA-N 0.000 description 2
- GLDOVTGHNKAZLK-UHFFFAOYSA-N octadecan-1-ol Chemical compound CCCCCCCCCCCCCCCCCCO GLDOVTGHNKAZLK-UHFFFAOYSA-N 0.000 description 2
- 229920000642 polymer Polymers 0.000 description 2
- 229920001282 polysaccharide Polymers 0.000 description 2
- 239000005017 polysaccharide Substances 0.000 description 2
- BWHMMNNQKKPAPP-UHFFFAOYSA-L potassium carbonate Chemical compound [K+].[K+].[O-]C([O-])=O BWHMMNNQKKPAPP-UHFFFAOYSA-L 0.000 description 2
- 239000002994 raw material Substances 0.000 description 2
- 229920006395 saturated elastomer Polymers 0.000 description 2
- 239000000344 soap Substances 0.000 description 2
- 239000000176 sodium gluconate Substances 0.000 description 2
- 235000012207 sodium gluconate Nutrition 0.000 description 2
- 229940005574 sodium gluconate Drugs 0.000 description 2
- 239000002904 solvent Substances 0.000 description 2
- 239000000126 substance Substances 0.000 description 2
- 150000003871 sulfonates Chemical class 0.000 description 2
- HLZKNKRTKFSKGZ-UHFFFAOYSA-N tetradecan-1-ol Chemical compound CCCCCCCCCCCCCCO HLZKNKRTKFSKGZ-UHFFFAOYSA-N 0.000 description 2
- KJIOQYGWTQBHNH-UHFFFAOYSA-N undecanol Chemical compound CCCCCCCCCCCO KJIOQYGWTQBHNH-UHFFFAOYSA-N 0.000 description 2
- CFOQKXQWGLAKSK-KTKRTIGZSA-N (13Z)-docosen-1-ol Chemical compound CCCCCCCC\C=C/CCCCCCCCCCCCO CFOQKXQWGLAKSK-KTKRTIGZSA-N 0.000 description 1
- 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
- ALSTYHKOOCGGFT-KTKRTIGZSA-N (9Z)-octadecen-1-ol Chemical compound CCCCCCCC\C=C/CCCCCCCCO ALSTYHKOOCGGFT-KTKRTIGZSA-N 0.000 description 1
- DJYWKXYRGAMLRE-QXMHVHEDSA-N (z)-icos-9-en-1-ol Chemical compound CCCCCCCCCC\C=C/CCCCCCCCO DJYWKXYRGAMLRE-QXMHVHEDSA-N 0.000 description 1
- TVPWKOCQOFBNML-SEYXRHQNSA-N (z)-octadec-6-en-1-ol Chemical compound CCCCCCCCCCC\C=C/CCCCCO TVPWKOCQOFBNML-SEYXRHQNSA-N 0.000 description 1
- RTBFRGCFXZNCOE-UHFFFAOYSA-N 1-methylsulfonylpiperidin-4-one Chemical class CS(=O)(=O)N1CCC(=O)CC1 RTBFRGCFXZNCOE-UHFFFAOYSA-N 0.000 description 1
- CFOQKXQWGLAKSK-UHFFFAOYSA-N 13-docosen-1-ol Natural products CCCCCCCCC=CCCCCCCCCCCCCO CFOQKXQWGLAKSK-UHFFFAOYSA-N 0.000 description 1
- POAOYUHQDCAZBD-UHFFFAOYSA-N 2-butoxyethanol Chemical compound CCCCOCCO POAOYUHQDCAZBD-UHFFFAOYSA-N 0.000 description 1
- JBVOQKNLGSOPNZ-UHFFFAOYSA-N 2-propan-2-ylbenzenesulfonic acid Chemical compound CC(C)C1=CC=CC=C1S(O)(=O)=O JBVOQKNLGSOPNZ-UHFFFAOYSA-N 0.000 description 1
- QGZKDVFQNNGYKY-UHFFFAOYSA-O Ammonium Chemical compound [NH4+] QGZKDVFQNNGYKY-UHFFFAOYSA-O 0.000 description 1
- VEXZGXHMUGYJMC-UHFFFAOYSA-M Chloride anion Chemical compound [Cl-] VEXZGXHMUGYJMC-UHFFFAOYSA-M 0.000 description 1
- KRKNYBCHXYNGOX-UHFFFAOYSA-K Citrate Chemical compound [O-]C(=O)CC(O)(CC([O-])=O)C([O-])=O KRKNYBCHXYNGOX-UHFFFAOYSA-K 0.000 description 1
- OCUCCJIRFHNWBP-IYEMJOQQSA-L Copper gluconate Chemical class [Cu+2].OC[C@@H](O)[C@@H](O)[C@H](O)[C@@H](O)C([O-])=O.OC[C@@H](O)[C@@H](O)[C@H](O)[C@@H](O)C([O-])=O OCUCCJIRFHNWBP-IYEMJOQQSA-L 0.000 description 1
- FEWJPZIEWOKRBE-JCYAYHJZSA-N Dextrotartaric acid Chemical compound OC(=O)[C@H](O)[C@@H](O)C(O)=O FEWJPZIEWOKRBE-JCYAYHJZSA-N 0.000 description 1
- RUPBZQFQVRMKDG-UHFFFAOYSA-M Didecyldimethylammonium chloride Chemical compound [Cl-].CCCCCCCCCC[N+](C)(C)CCCCCCCCCC RUPBZQFQVRMKDG-UHFFFAOYSA-M 0.000 description 1
- 102000004190 Enzymes Human genes 0.000 description 1
- 108090000790 Enzymes Proteins 0.000 description 1
- IAYPIBMASNFSPL-UHFFFAOYSA-N Ethylene oxide Chemical compound C1CO1 IAYPIBMASNFSPL-UHFFFAOYSA-N 0.000 description 1
- 108010010803 Gelatin Proteins 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
- 239000005639 Lauric acid Substances 0.000 description 1
- 229910019142 PO4 Inorganic materials 0.000 description 1
- ABLZXFCXXLZCGV-UHFFFAOYSA-N Phosphorous acid Chemical class OP(O)=O ABLZXFCXXLZCGV-UHFFFAOYSA-N 0.000 description 1
- 235000008331 Pinus X rigitaeda Nutrition 0.000 description 1
- 235000011613 Pinus brutia Nutrition 0.000 description 1
- 241000018646 Pinus brutia Species 0.000 description 1
- 239000002202 Polyethylene glycol Substances 0.000 description 1
- ZLMJMSJWJFRBEC-UHFFFAOYSA-N Potassium Chemical compound [K] ZLMJMSJWJFRBEC-UHFFFAOYSA-N 0.000 description 1
- GOOHAUXETOMSMM-UHFFFAOYSA-N Propylene oxide Chemical compound CC1CO1 GOOHAUXETOMSMM-UHFFFAOYSA-N 0.000 description 1
- FEWJPZIEWOKRBE-UHFFFAOYSA-N Tartaric acid Natural products [H+].[H+].[O-]C(=O)C(O)C(O)C([O-])=O FEWJPZIEWOKRBE-UHFFFAOYSA-N 0.000 description 1
- 150000007513 acids Chemical class 0.000 description 1
- 230000000996 additive effect Effects 0.000 description 1
- 239000001361 adipic acid Substances 0.000 description 1
- 235000011037 adipic acid Nutrition 0.000 description 1
- 150000001299 aldehydes Chemical class 0.000 description 1
- 229910052784 alkaline earth metal Inorganic materials 0.000 description 1
- 150000003973 alkyl amines Chemical class 0.000 description 1
- 150000004996 alkyl benzenes Chemical class 0.000 description 1
- 125000005907 alkyl ester group Chemical group 0.000 description 1
- 150000001350 alkyl halides Chemical class 0.000 description 1
- 150000003863 ammonium salts Chemical class 0.000 description 1
- JFCQEDHGNNZCLN-UHFFFAOYSA-N anhydrous glutaric acid Natural products OC(=O)CCCC(O)=O JFCQEDHGNNZCLN-UHFFFAOYSA-N 0.000 description 1
- 150000001450 anions Chemical class 0.000 description 1
- 229940027983 antiseptic and disinfectant quaternary ammonium compound Drugs 0.000 description 1
- 239000002216 antistatic agent Substances 0.000 description 1
- PYMYPHUHKUWMLA-UHFFFAOYSA-N arabinose Natural products OCC(O)C(O)C(O)C=O PYMYPHUHKUWMLA-UHFFFAOYSA-N 0.000 description 1
- 239000002585 base Substances 0.000 description 1
- KCXMKQUNVWSEMD-UHFFFAOYSA-N benzyl chloride Chemical compound ClCC1=CC=CC=C1 KCXMKQUNVWSEMD-UHFFFAOYSA-N 0.000 description 1
- 229940073608 benzyl chloride Drugs 0.000 description 1
- SRBFZHDQGSBBOR-UHFFFAOYSA-N beta-D-Pyranose-Lyxose Natural products OC1COC(O)C(O)C1O SRBFZHDQGSBBOR-UHFFFAOYSA-N 0.000 description 1
- 238000004061 bleaching Methods 0.000 description 1
- KDYFGRWQOYBRFD-NUQCWPJISA-N butanedioic acid Chemical class O[14C](=O)CC[14C](O)=O KDYFGRWQOYBRFD-NUQCWPJISA-N 0.000 description 1
- 239000004202 carbamide Substances 0.000 description 1
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- 239000006229 carbon black Substances 0.000 description 1
- 150000003857 carboxamides Chemical class 0.000 description 1
- 125000002091 cationic group Chemical group 0.000 description 1
- 229960000541 cetyl alcohol Drugs 0.000 description 1
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- MWKFXSUHUHTGQN-UHFFFAOYSA-N decan-1-ol Chemical compound CCCCCCCCCCO MWKFXSUHUHTGQN-UHFFFAOYSA-N 0.000 description 1
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- 239000008103 glucose Substances 0.000 description 1
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- 125000002887 hydroxy group Chemical group [H]O* 0.000 description 1
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- GOQYKNQRPGWPLP-UHFFFAOYSA-N n-heptadecyl alcohol Natural products CCCCCCCCCCCCCCCCCO GOQYKNQRPGWPLP-UHFFFAOYSA-N 0.000 description 1
- UZZYXUGECOQHPU-UHFFFAOYSA-M n-octyl sulfate Chemical compound CCCCCCCCOS([O-])(=O)=O UZZYXUGECOQHPU-UHFFFAOYSA-M 0.000 description 1
- 230000007935 neutral effect Effects 0.000 description 1
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- ALSTYHKOOCGGFT-MDZDMXLPSA-N oleyl alcohol Chemical compound CCCCCCCC\C=C\CCCCCCCCO ALSTYHKOOCGGFT-MDZDMXLPSA-N 0.000 description 1
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- XMLQWXUVTXCDDL-UHFFFAOYSA-N oleyl alcohol Natural products CCCCCCC=CCCCCCCCCCCO XMLQWXUVTXCDDL-UHFFFAOYSA-N 0.000 description 1
- 239000003605 opacifier Substances 0.000 description 1
- IPCSVZSSVZVIGE-UHFFFAOYSA-N palmitic acid group Chemical group C(CCCCCCCCCCCCCCC)(=O)O IPCSVZSSVZVIGE-UHFFFAOYSA-N 0.000 description 1
- 235000021317 phosphate Nutrition 0.000 description 1
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- 229920005646 polycarboxylate Polymers 0.000 description 1
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- 229910052700 potassium Inorganic materials 0.000 description 1
- 239000011591 potassium Substances 0.000 description 1
- 235000015497 potassium bicarbonate Nutrition 0.000 description 1
- 229910000027 potassium carbonate Inorganic materials 0.000 description 1
- 235000011181 potassium carbonates Nutrition 0.000 description 1
- 239000003755 preservative agent Substances 0.000 description 1
- 150000003138 primary alcohols Chemical class 0.000 description 1
- 239000000047 product Substances 0.000 description 1
- 239000011814 protection agent Substances 0.000 description 1
- 150000003856 quaternary ammonium compounds Chemical class 0.000 description 1
- 230000002441 reversible effect Effects 0.000 description 1
- 238000010850 salt effect Methods 0.000 description 1
- 150000004671 saturated fatty acids Chemical class 0.000 description 1
- 235000003441 saturated fatty acids Nutrition 0.000 description 1
- 238000005204 segregation Methods 0.000 description 1
- 238000000926 separation method Methods 0.000 description 1
- 239000002453 shampoo Substances 0.000 description 1
- 229910052708 sodium Inorganic materials 0.000 description 1
- 239000011734 sodium Substances 0.000 description 1
- 229910000029 sodium carbonate Inorganic materials 0.000 description 1
- 239000001509 sodium citrate Substances 0.000 description 1
- 239000002689 soil Substances 0.000 description 1
- 239000007921 spray Substances 0.000 description 1
- 239000007785 strong electrolyte Substances 0.000 description 1
- 239000001384 succinic acid Substances 0.000 description 1
- 230000019635 sulfation Effects 0.000 description 1
- 238000005670 sulfation reaction Methods 0.000 description 1
- UZZYXUGECOQHPU-UHFFFAOYSA-N sulfuric acid monooctyl ester Natural products CCCCCCCCOS(O)(=O)=O UZZYXUGECOQHPU-UHFFFAOYSA-N 0.000 description 1
- 229920001059 synthetic polymer Polymers 0.000 description 1
- 239000011975 tartaric acid Substances 0.000 description 1
- 235000002906 tartaric acid Nutrition 0.000 description 1
- 238000010998 test method Methods 0.000 description 1
- 150000005621 tetraalkylammonium salts Chemical class 0.000 description 1
- 125000005208 trialkylammonium group Chemical group 0.000 description 1
- UFTFJSFQGQCHQW-UHFFFAOYSA-N triformin Chemical compound O=COCC(OC=O)COC=O UFTFJSFQGQCHQW-UHFFFAOYSA-N 0.000 description 1
- 229940057402 undecyl alcohol Drugs 0.000 description 1
- 239000003021 water soluble solvent Substances 0.000 description 1
- 239000000230 xanthan gum Substances 0.000 description 1
- 229920001285 xanthan gum Polymers 0.000 description 1
- 229940082509 xanthan gum Drugs 0.000 description 1
- 235000010493 xanthan gum Nutrition 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
- 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
- C11D3/02—Inorganic compounds ; Elemental compounds
- C11D3/04—Water-soluble compounds
- C11D3/06—Phosphates, including polyphosphates
-
- 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
- C11D3/2075—Carboxylic acids-salts thereof
- C11D3/2086—Hydroxy carboxylic acids-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
- C11D1/12—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
- C11D1/66—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
- C11D1/72—Ethers of polyoxyalkylene glycols
Definitions
- the invention relates to the use of aqueous multiphase liquid surfactant Detergents that can be temporarily emulsified by shaking and for cleaning hard surfaces can be used.
- all-purpose cleaners represent predominantly neutral to weakly alkaline aqueous liquid products, the 1 to 30% by weight surfactants, 0 to 5% by weight builder (e.g. citrates, gluconates, soda, polycarboxylates) 0 to 10% by weight of hydrotropes (e.g. alcohols, urea), 0 to 10% by weight of water-soluble Solvents (e.g. alcohols, glycol ethers) and optionally, among others Skin protection, coloring and Contain fragrances. It is usually used as an approx. 1% solution in water local stain removal also undiluted. There are also ready-to-use all-purpose cleaners as a so-called spray cleaner in the trade.
- Such aqueous liquid cleaners are usually homogeneous or stable solutions Dispersions.
- the use of certain, especially hydrophobic, components in such cleaning agents can, however, result in this homogeneity being lost and inhomogeneous agents are obtained, their acceptance by the consumer as low is to be assessed.
- the alternative formulation of funds is required despite its inhomogeneity, it is a defined exterior that is acceptable to the consumer Show appearance and application form.
- European patent application 116 422 describes a liquid hair or body shampoo with two aqueous phases which can be temporarily dispersed into one another by shaking, and both phases being miscible with water in any ratio.
- the upper phase contains 8 to 25% by weight, based on the total composition, of at least one surfactant and the lower phase contains at least 6% by weight, based on the total composition, of dissolved sodium hexametaphosphate of the formula I, in which n stands for an average of approximately 12. Additional builder salts can optionally be included in the lower phase.
- Anionic, cationic, amphoteric and / or nonionic surfactants can be present as surfactants, preferably at least one anionic surfactant being contained.
- the object of the present invention was to provide powerful and storage-stable agents Cleaning of hard surfaces in defined inhomogeneous, easy to handle and for the Provide consumers with acceptable form.
- the invention relates to the use of a aqueous liquid multi-phase surfactant-containing cleaning agent with at least two continuous phases, the at least one lower aqueous phase I and one with this Has phase immiscible upper aqueous phase II and temporarily shaken in an emulsion can be transferred, the agent one or more hydrophobic Has components and contains 0 to 5 wt .-% sodium hexametaphosphate.
- sodium hexametaphosphate is to be understood as a mixture of condensed orthophosphates of the formula I, where n is an average of about 12.
- an agent according to the invention consists of a lower continuous one Phase consisting of the entire phase I and an upper continuous phase consisting of of the entire phase II.
- agents according to the invention can also emulsify parts of another phase Contain form, so that in such an agent, for example, phase I in part as continuous phase I is present, which is the lower continuous phase of the agent, and to a different extent than discontinuous phase I in the upper continuous phase II is emulsified.
- phase II and other continuous phases are examples of phase II and other continuous phases.
- temporary is to be understood to mean that 90% of the demixing of the emulsion formed by shaking into the separate phases at temperatures of about 20 ° C. to about 40 ° C. takes place within 2 minutes to 10 hours and the last 2 % of the segregation into the phase state before shaking can take place within a further 15 minutes to 50 hours.
- the invention relates to the use of a second embodiment aqueous liquid multi-phase surfactant-containing cleaning agent with at least two continuous phases, the at least one lower aqueous phase I and one with this Has phase immiscible upper aqueous phase II and temporarily shaken in an emulsion can be transferred, for cleaning hard surfaces, the agent one or has several hydrophobic components.
- the following statements relate to the agents according to the invention, they apply equally to the agents of use according to the invention.
- the agents according to the invention are characterized by an unusually good cleaning performance of stubborn grease dirt when used undiluted. Furthermore the agents show a favorable residue behavior.
- the individual phases are on average stable for a long time without e.g. Deposits formed, and the transfer into a temporary emulsion remains reversible even after frequent shaking.
- the Separation of ingredients in separate phases promote the chemical stability of the agent.
- the invention also relates to a process for producing an agent according to the invention by mixing it directly from its raw materials, then mixing it and finally standing the agent to separate the temporary emulsion.
- the continuous phases I and II are delimited from one another by a sharp interface.
- one or both of the continuous phases I and II parts preferably 0.1 to 25 vol .-%, in particular 0.2 to 15 vol .-%, based on the volume of the respective continuous phase, each phase other than dispersant.
- the continuous phase I or II is then around Volume part reduced, which is distributed as a dispersant in the other phase.
- Especially agents in which phase I in amounts of 0.1 to 25% by volume are preferred 0.2 to 15 vol .-%, based on the volume of phase II, is emulsified in phase II.
- a further preferred usable embodiment of the invention lies next to the continuous phases I and II part of the two phases as an emulsion of one of the two Phases in the other phase, this emulsion being separated by two sharp interfaces, an upper and a lower, compared to the parts of the Phases I and II are delimited.
- the agents which can be used according to the invention contain phase I and phase II in one Volume ratio of 90:10 to 10:90, preferably 75:25 to 25:75, in particular 65: 35 to 35: 65.
- the cleaning agents that can be used contain one or more hydrophobic components.
- Suitable hydrophobic components are, for example, dialkyl ethers with identical or different C 4 -C 14 -alkyl radicals, in particular dioctyl ether; Hydrocarbons with a boiling range from 100 to 300 ° C, in particular 140 to 280 ° C, for example aliphatic hydrocarbons with a boiling range from 145 to 200 ° C, isoparaffins with a boiling range from 200 to 260 ° C; essential oils, in particular limonene and pine oil extracted from pine roots and stumps; and also mixtures of these hydrophobic components, in particular mixtures of two or three of the hydrophobic components mentioned.
- Preferred mixtures of hydrophobic components are mixtures of various dialkyl ethers, of dialkyl ethers and hydrocarbons, of dialkyl ethers and essential oils, of hydrocarbons and essential oils, of dialkyl ethers and hydrocarbons and essential oils and of these mixtures.
- the compositions contain hydrophobic components in amounts, based on the composition, of 0 to 20% by weight, preferably 0.1 to 14% by weight, in particular 0.5 to 10% by weight, most preferably 0.8 to 7 wt .-%.
- phase separation aids are, for example, the alkali metal and Alkaline earth metal chlorides and sulfates, especially sodium and potassium chloride and sulfate, and ammonium chloride and sulfate or mixtures thereof.
- the salts mentioned as strong electrolytes support phase separation through the salt effect.
- Builder salts act as electrolytes and are therefore suitable also as phase separation aid.
- the agents contain phase separation aids in quantities, based on the composition, from 0 to 30% by weight, preferably 1 to 20% by weight, in particular 3 to 15% by weight, most preferably 5 to 12% by weight.
- the agents used according to the invention can be anionic, non-ionic, amphoteric or cationic surfactants or surfactant mixtures of one or more or contain all of these classes of surfactants.
- the detergents contain surfactants in quantities on the composition, from 0.01 to 30% by weight, preferably 0.1 to 20% by weight, in particular 1 to 14% by weight, most preferably 3 to 10% by weight.
- Suitable nonionic surfactants are, for example, C 8 -C 18 alkyl alcohol polyglycol ethers, alkyl polyglycosides and nitrogen-containing surfactants or mixtures thereof, in particular the first two.
- the compositions contain nonionic surfactants in amounts, based on the composition, of 0 to 30% by weight, preferably 0.1 to 20% by weight, in particular 0.5 to 14% by weight, extremely preferably 1 to 10% by weight .-%.
- C 8 -C 18 alkyl alcohol polypropylene glycol / polyethylene glycol ethers are preferred known nonionic surfactants. They can be described by the formula II, R i O- (CH 2 CH (CH 3 ) O) p (CH 2 CH 2 O) e -H in which R i is a linear or branched, aliphatic alkyl and / or alkenyl radical having 8 to 18 carbon atoms, p is 0 or numbers from 1 to 3 and e is numbers from 1 to 20.
- the C 8 -C 18 alkyl alcohol polyglycol ethers of the formula II can be obtained by addition of propylene oxide and / or ethylene oxide to alkyl alcohols, preferably to fatty alcohols.
- Typical examples are polyglycol ethers of the formula II in which R i is an alkyl radical having 8 to 18 carbon atoms, p is 0 to 2 and e is a number from 2 to 7.
- End-capped C 8 -C 18 -alkyl alcohol polyglycol ethers can also be used, ie compounds in which the free OH group in the formula II is etherified.
- C 8 -C 18 alkyl alcohol polyglycol ethers can be obtained by the relevant methods of preparative organic chemistry.
- C 8 -C 18 -Alkyl alcohol polyglycol ethers are preferably reacted in the presence of bases with alkyl halides, in particular butyl or benzyl chloride.
- Typical examples are mixed ethers of the formula II in which R i stands for an industrial fatty alcohol residue, preferably C 12/14 cocoalkyl residue, p for 0 and e for 5 to 10, which are sealed with a butyl group.
- Preferred nonionic surfactants are furthermore alkyl polyglycosides (APG) of the formula III, R ii O [G] x , in which R ii for a linear or branched, saturated or unsaturated alkyl radical having 8 to 22 carbon atoms, [G] for a glycosidically linked sugar radical and x stands for a number from 1 to 10.
- APG are non-ionic surfactants and are known substances that can be obtained using the relevant methods of preparative organic chemistry.
- the index number x in the general formula III indicates the degree of oligomerization (DP degree), ie the distribution of mono- and oligoglycosides, and stands for a number between 1 and 10.
- Alkyl glycosides with an average degree of oligomerization x of 1.1 to 3.0 are preferably used. From an application point of view, those alkyl glycosides are preferred whose degree of oligomerization is less than 1.7 and in particular between 1.2 and 1.6.
- Xylose, but especially glucose, is preferably used as the glycosidic sugar.
- the alkyl or alkenyl radical R ii (formula III) can be derived from primary alcohols having 8 to 18, preferably 8 to 14, carbon atoms. Typical examples are capronic alcohol, caprylic alcohol, capric alcohol and undecyl alcohol and their technical mixtures, such as those obtained in the course of the hydrogenation of technical fatty acid methyl esters or in the course of the hydrogenation of aldehydes from ROELEN's oxosynthesis.
- the alkyl or alkenyl radical R ii is preferably derived from lauryl alcohol, myristyl alcohol, cetyl alcohol, palmoleyl alcohol, stearyl alcohol, isostearyl alcohol or oleyl alcohol. Elaidyl alcohol, petroselinyl alcohol, arachidyl alcohol, gadoleyl alcohol, behenyl alcohol, erucyl alcohol and their technical mixtures are also to be mentioned.
- Nitrogen-containing surfactants may be included as further nonionic surfactants, e.g. Fatty acid polyhydroxyamides, for example glucamides, and ethoxylates of alkylamines, vicinal diols and / or carboxamides, the alkyl groups with 10 to 22 carbon atoms, preferably have 12 to 18 carbon atoms.
- the degree of ethoxylation of these compounds is generally between 1 and 20, preferably between 3 and 10.
- the particularly suitable compounds include the lauric acid, Myristic and palmitic monoethanolamides.
- Suitable anionic surfactants are the preferred C 8 -C 18 alkyl sulfates, C 8 -C 18 alkyl ether sulfates, ie the sulfation products of the alcohol ethers of the formula II, and / or C 8 -C 18 alkyl benzene sulfonates, but also C 8 -C 18 alkanesulfonates , C 8 -C 18 - ⁇ -olefin sulfonates, sulfonated C 8 -C 18 fatty acids, especially dodecylbenzenesulfonate, C 8 -C 22 carboxamide amide ether sulfates, sulfonic succinic acid mono- and di-C 1 -C 12 alkyl esters, C 8 -C 18 -Alkylpolyglykolethercarboxylate, C 8 -C 18 -N-acyl taurides, C 8 -C 18 -N-sarco
- compositions contain anionic surfactants in amounts, based on the composition, of 0 to 30% by weight, preferably 0.1 to 20% by weight, in particular 1 to 14% by weight, extremely preferably 2 to 10% by weight. %.
- the agents according to the invention can also contain soaps, ie alkali metal or ammonium salts of saturated or unsaturated C 6 -C 22 fatty acids.
- the soaps can be used in an amount of up to 5% by weight, preferably from 0.1 to 2% by weight.
- Suitable amphoteric surfactants are, for example, betaines of the formula (R iii ) (R iv ) (R v ) N + CH 2 COO - , in which R iii is an alkyl radical with 8 to 25, preferably 10 to 21, carbon atoms and R, which is optionally interrupted by heteroatoms or heteroatom groups iv and R v are identical or different alkyl radicals having 1 to 3 carbon atoms, in particular C 10 -C 18 -alkyldimethylcarboxymethylbetaine and C 11 -C 17 -alkylamidopropyldimethylcarboxymethylbetaine.
- the compositions contain amphoteric surfactants in amounts, based on the composition, of 0 to 15% by weight, preferably 0.01 to 10% by weight, in particular 0.1 to 5% by weight.
- Suitable cationic surfactants include the quaternary ammonium compounds of the formula (R vi ) (R vii ) (R viii ) (R ix ) N + X - , in which R vi to R ix for four identical or different types, in particular two long and two short-chain, alkyl radicals and X - represent an anion, in particular a halide ion, for example didecyldimethylammonium chloride, alkylbenzyldidecylammonium chloride and mixtures thereof.
- the compositions contain cationic surfactants in amounts, based on the composition, of 0 to 10% by weight, preferably 0.01 to 5% by weight, in particular 0.1 to 3% by weight.
- the agents according to the invention contain anionic and nonionic surfactants next to one another, preferably C 8 -C 18 alkylbenzenesulfonates, C 8 -C 18 alkyl sulfates and / or C 8 -C 18 alkyl ether sulfates in addition to C 8 -C 18 alkyl alcohol polyglycol ethers and / or alkyl polyglycosides, in particular C 8 -C 18 alkylbenzenesulfonates in addition to C 8 -C 18 alkyl alcohol polyglycol ethers.
- anionic and nonionic surfactants next to one another preferably C 8 -C 18 alkylbenzenesulfonates, C 8 -C 18 alkyl sulfates and / or C 8 -C 18 alkyl ether sulfates in addition to C 8 -C 18 alkyl alcohol polyglycol ethers.
- the agents according to the invention can also contain builders. Suitable builders are for example alkali metal gluconates, citrates, nitrilotriacetates, carbonates and bicarbonates, in particular sodium gluconate, citrate and nitrilotriacetate as well as sodium and Potassium carbonate and bicarbonate, as well as alkali metal and alkaline earth metal hydroxides, especially sodium and potassium hydroxide, ammonia and amines, especially monound Triethanolamine, or their mixtures. This also includes the salts of glutaric acid, Succinic acid, adipic acid, tartaric acid and benzene hexacarboxylic acid as well as phosphonates and Phosphates.
- Suitable builders are for example alkali metal gluconates, citrates, nitrilotriacetates, carbonates and bicarbonates, in particular sodium gluconate, citrate and nitrilotriacetate as well as sodium and Potassium carbonate and bicarbon
- the agents contain builders in amounts, based on the composition, of 0 to 20% by weight, preferably 0.01 to 12% by weight, in particular 0.1 to 8% by weight, extremely preferably 0.3 to 5% by weight, but the amount of sodium hexametaphosphate except for the agents used - is limited to 0 to 5 wt .-%.
- Electrolytes are the builder salts at the same time phase separation aids.
- the agents according to the invention can contain further auxiliaries and additives as are customary in such agents.
- auxiliaries and additives include in particular polymers, soil release agents, solvents (e.g. ethanol, isopropanol, glycol ether), solubilizers, hydrotropes (e.g. cumene sulfonate, octyl sulfate, butyl glucoside, butyl glycol), cleaning enhancers, viscosity regulators (e.g. synthetic polymers such as polysaccharides, polyacrylates, in nature occurring polymers and their derivatives such as xanthan gum, other polysaccharides and / or gelatin), pH regulators (e.g.
- the amount of such additives is usually not more than 12% by weight in the cleaning agent.
- the lower limit of use depends on the type of additive and can be up to 0.001% by weight and below, for example, for dyes.
- the amount of auxiliaries is preferably between 0.01 and 7% by weight, in particular 0.1 and 4% by weight.
- the pH of the agents according to the invention can be varied over a wide range, but a range from 2.5 to 12, in particular 5 to 10.5, is preferred.
- the pH of the agents according to the invention is understood to mean the pH of the agent in the form of the temporary emulsion.
- the agents according to the invention can be mixed directly from their raw materials, then mixing and finally standing the means for separating the temporary emulsion.
- the cleaning agent to be tested was then placed on an artificially soiled white plastic surface.
- a mixture of carbon black, machine oil, triglyceride of saturated fatty acids and low-boiling aliphatic hydrocarbon was used as artificial soiling for the dilute use of the cleaning agent.
- the test area of 26 x 28 cm was evenly coated with 2 g of the artificial soiling with the aid of a surface coater.
- a plastic sponge was each with 10 ml of the detergent solution to be tested impregnated and mechanically on the detergent also to be tested with 10 ml coated test surface moves. After 10 wiping movements, the cleaned test area Held under running water and the loose dirt removed. The cleaning effect, i.e. the whiteness of the so-called plastic surface was measured with a Color difference measuring device "Microcolor" (Dr. Lange) measured. The served as the white standard clean untreated white plastic surface.
- the test was carried out with the inventive cleaning agent E1 in diluted usage at a concentration of 6 MLL -1 and in undiluted.
- the test was carried out with a leading all-purpose cleaner in the German market with more than 10% by weight of surfactants ( V1 ) in dilute application of 6 ml ⁇ l -1 as well as in undiluted application.
- the inventive cleaning agent E1 outperforms the significantly more surfactant-rich cleaner V1 in both the diluted application and in the undiluted application.
- the residue behavior was checked on black tiles.
- the backlog of the The agent according to the invention is at the level of commercially available all-purpose cleaners in Germany. This is still the case even if the agent contains hydrophobic components contain.
- phase I [% by weight]
- Phase II [% by weight] a) 0 6.2 c) ⁇ 0.05 3.3 d) 1.06 1.0 f) 11.5 8.9 j) ⁇ 0.05 7.9 k) ⁇ 0.05 1.6 l) 85.0 70.7
- the upper phase II contains almost the entire amount of surfactant (a, c), hydrophobic component (j) and perfume (k), while the lower phase I almost exclusively a part of the Phase separation aid (f) and the builder (d) contains.
Landscapes
- Chemical & Material Sciences (AREA)
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- Engineering & Computer Science (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Oil, Petroleum & Natural Gas (AREA)
- Wood Science & Technology (AREA)
- Organic Chemistry (AREA)
- Health & Medical Sciences (AREA)
- Emergency Medicine (AREA)
- Inorganic Chemistry (AREA)
- Detergent Compositions (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
Abstract
Description
Die Erfindung betrifft die Verwendung wässriger mehrphasiger flüssiger tensidhaltiger Reinigungsmittel, die sich durch Schütteln temporär emulgieren lassen und zur Reinigung harter Oberflächen einsetzbar sind.The invention relates to the use of aqueous multiphase liquid surfactant Detergents that can be temporarily emulsified by shaking and for cleaning hard surfaces can be used.
Universell verwendbare Reinigungsmittel für alle harten, nass oder feucht abwischbaren Oberflächen im Haushalt und Gewerbe sind als sogenannte Allzweckreiniger bekannt und stellen überwiegend neutral bis schwach alkalische wässrige Flüssigprodukte dar, die 1 bis 30 Gew.-% Tenside, 0 bis 5 Gew.-% Builder (z.B. Citrate, Gluconate, Soda, Polycarboxylate) 0 bis 10 Gew.-% Hydrotrope (z.B. Alkohole, Harnstoff), 0 bis 10 Gew.-% wasserlösliche Lösungsmittel (z.B. Alkohole, Glykolether) sowie wahlweise u.a. Hautschutzmittel, Farb- und Duftstoffe enthalten. Die Verwendung erfolgt meist als ca. 1 %ige Lösung in Wasser, zur lokalen Fleckentfernung auch unverdünnt. Daneben sind gebrauchsfertige Allzweckreiniger als sogenannte Sprühreiniger im Handel.Universally usable cleaning agents for all hard, wet or damp wipeable Household and commercial surfaces are known as so-called all-purpose cleaners represent predominantly neutral to weakly alkaline aqueous liquid products, the 1 to 30% by weight surfactants, 0 to 5% by weight builder (e.g. citrates, gluconates, soda, polycarboxylates) 0 to 10% by weight of hydrotropes (e.g. alcohols, urea), 0 to 10% by weight of water-soluble Solvents (e.g. alcohols, glycol ethers) and optionally, among others Skin protection, coloring and Contain fragrances. It is usually used as an approx. 1% solution in water local stain removal also undiluted. There are also ready-to-use all-purpose cleaners as a so-called spray cleaner in the trade.
Derartige wäßrige Flüssigreiniger liegen üblicherweise als homogene stabile Lösungen oder Dispersionen vor. Der Einsatz bestimmter, insbesondere hydrophober, Komponenten in solchen Reinigungsmitteln kann jedoch dazu führen, daß diese Homogenität verloren geht und inhomogene Mittel erhalten werden, deren Akzeptanz beim Verbraucher als gering einzuschätzen ist. In solchen Fällen bedarf es der alternativen Formulierung von Mitteln, die trotz ihrer Inhomogenität eine definierte und für den Verbraucher akzeptable äußere Erscheinungs- und Anwendungsform aufweisen.Such aqueous liquid cleaners are usually homogeneous or stable solutions Dispersions. The use of certain, especially hydrophobic, components in such cleaning agents can, however, result in this homogeneity being lost and inhomogeneous agents are obtained, their acceptance by the consumer as low is to be assessed. In such cases, the alternative formulation of funds is required despite its inhomogeneity, it is a defined exterior that is acceptable to the consumer Show appearance and application form.
Die europäische Patentanmeldung 116 422 beschreibt ein flüssiges Haar- oder Körpershampoo
mit zwei wäßrigen Phasen, die durch Schütteln temporär ineinander dispergierbar
sind und wobei beide Phasen mit Wasser in beliebigem Verhältnis mischbar sind. Die obere
Phase enthält hierbei 8 bis 25 Gew.-%, bezogen auf die Gesamtzusammensetzung, von
mindestens einem Tensid und die untere Phase mindestens 6 Gew.-%, bezogen auf die
Gesamtzusammensetzung, an gelöstem Natriumhexametaphosphat der Formel I,
Aufgabe der vorliegenden Erfindung war es, leistungsstarke und lagerstabile Mittel zur Reinigung harter Oberflächen in definierter inhomogener, leicht handhabbarer und für den Verbraucher akzeptabler Form bereitzustellen.The object of the present invention was to provide powerful and storage-stable agents Cleaning of hard surfaces in defined inhomogeneous, easy to handle and for the Provide consumers with acceptable form.
Gegenstand der Erfindung ist in einer ersten Ausführungsform die Verwendung eines wässrigen flüssigen mehrphasigen tensidhaltigen Reinigungsmittels mit wenigstens zwei kontinuierlichen Phasen, das mindestens eine untere wässrige Phase I sowie eine mit dieser Phase nicht mischbare obere wässrige Phase II aufweist und sich durch Schütteln temporär in eine Emulsion überführen lässt, wobei das Mittel eine oder mehrere hydrophobe Komponenten aufweist und das 0 bis 5 Gew.-% Natriumhexametaphosphat enthält.In a first embodiment, the invention relates to the use of a aqueous liquid multi-phase surfactant-containing cleaning agent with at least two continuous phases, the at least one lower aqueous phase I and one with this Has phase immiscible upper aqueous phase II and temporarily shaken in an emulsion can be transferred, the agent one or more hydrophobic Has components and contains 0 to 5 wt .-% sodium hexametaphosphate.
Unter Natriumhexametaphosphat ist im Rahmen der vorliegenden Erfindung eine Mischung kondensierter Orthophosphate der Formel I zu verstehen, wobei n für einen Mittelwert von etwa 12 steht.In the context of the present invention, sodium hexametaphosphate is to be understood as a mixture of condensed orthophosphates of the formula I, where n is an average of about 12.
Im einfachsten Fall besteht ein erfindungsgemäßes Mittel aus einer unteren kontinuierlichen Phase, die aus der gesamten Phase I besteht, und einer oberen kontinuierlichen Phase, die aus der gesamten Phase II besteht. Eine oder mehrere kontinuierliche Phasen eines erfindungsgemäßen Mittels können jedoch auch Teile einer anderen Phase in emulgierter Form enthalten, so dass in einem solchen Mittel beispielsweise Phase I zu einem Teil als kontinuierliche Phase I vorliegt, die die untere kontinuierliche Phase des Mittels darstellt, und zu einem anderen Teil als diskontinuierliche Phase I in der oberen kontinuierlichen Phase II emulgiert ist. Für Phase II und weitere kontinuierliche Phasen gilt Analoges. In the simplest case, an agent according to the invention consists of a lower continuous one Phase consisting of the entire phase I and an upper continuous phase consisting of of the entire phase II. One or more continuous phases of one However, agents according to the invention can also emulsify parts of another phase Contain form, so that in such an agent, for example, phase I in part as continuous phase I is present, which is the lower continuous phase of the agent, and to a different extent than discontinuous phase I in the upper continuous phase II is emulsified. The same applies to phase II and other continuous phases.
Im Rahmen der vorliegenden Erfindung ist unter temporär zu verstehen, dass 90 % der Entmischung der durch Schütteln gebildeten Emulsion in die getrennten Phasen bei Temperaturen von etwa 20 °C bis ca. 40 °C innerhalb von 2 Minuten bis 10 Stunden erfolgt und die letzten 2 % der Entmischung in den Phasenzustand vor dem Schütteln innerhalb von weiteren 15 Minuten bis 50 Stunden erfolgen.In the context of the present invention, temporary is to be understood to mean that 90% of the demixing of the emulsion formed by shaking into the separate phases at temperatures of about 20 ° C. to about 40 ° C. takes place within 2 minutes to 10 hours and the last 2 % of the segregation into the phase state before shaking can take place within a further 15 minutes to 50 hours.
Gegenstand der Erfindung ist in einer zweiten Ausführungsform die Verwendung eines wässrigen flüssigen mehrphasigen tensidhaltigen Reinigungsmittels mit wenigstens zwei kontinuierlichen Phasen, das mindestens eine untere wässrige Phase I sowie eine mit dieser Phase nicht mischbare obere wässrige Phase II aufweist und sich durch Schütteln temporär in eine Emulsion überführen lässt, zur Reinigung harter Oberflächen, wobei das Mittel eine oder mehrere hydrophobe Komponenten aufweist. Insofern sich die folgenden Ausführungen auf die erfindungsgemäßen Mittel beziehen, gelten sie gleichermaßen für die Mittel der erfindungsgemäßen Verwendung.The invention relates to the use of a second embodiment aqueous liquid multi-phase surfactant-containing cleaning agent with at least two continuous phases, the at least one lower aqueous phase I and one with this Has phase immiscible upper aqueous phase II and temporarily shaken in an emulsion can be transferred, for cleaning hard surfaces, the agent one or has several hydrophobic components. In this respect, the following statements relate to the agents according to the invention, they apply equally to the agents of use according to the invention.
Die erfindungsgemäßen Mittel zeichnen sich durch eine ungewöhnlich gute Reinigungsleistung an hartnäckigem Fettschmutz bei unverdünnter Anwendung aus. Darüber hinaus zeigen die Mittel ein günstiges Rückstandsverhalten. Die einzelnen Phasen im Mittel sind über lange Zeit stabil, ohne dass sich z.B. Ablagerungen bildeten, und die Überführung in eine temporäre Emulsion bleibt auch nach häufigem Schütteln reversibel. Zudem kann die Trennung von Inhaltsstoffen in separate Phasen die chemische Stabilität des Mittels fördern.The agents according to the invention are characterized by an unusually good cleaning performance of stubborn grease dirt when used undiluted. Furthermore the agents show a favorable residue behavior. The individual phases are on average stable for a long time without e.g. Deposits formed, and the transfer into a temporary emulsion remains reversible even after frequent shaking. In addition, the Separation of ingredients in separate phases promote the chemical stability of the agent.
Auch Gegenstand der Erfindung ist ein Verfahren zur Herstellung eines erfindungsgemäßen
Mittels durch Aufmischen unmittelbar aus seinen Rohstoffen, anschließendes Durchmischen
und abschließendes Stehen des Mittels zur Auftrennung der temporären Emulsion.
In einer bevorzugten verwendbaren Ausführungsform der Erfindung sind die kontinuierlichen
Phasen I und II durch eine scharfe Grenzfläche gegeneinander abgegrenzt. The invention also relates to a process for producing an agent according to the invention by mixing it directly from its raw materials, then mixing it and finally standing the agent to separate the temporary emulsion.
In a preferred embodiment of the invention that can be used, the continuous phases I and II are delimited from one another by a sharp interface.
In einer weiteren bevorzugten Ausführungsform der Erfindung enthalten eine oder beide der kontinuierlichen Phasen I und II Teile, vorzugsweise 0,1 bis 25 Vol.-%, insbesondere 0,2 bis 15 Vol.-%, bezogen auf das Volumen der jeweiligen kontinuierlichen Phase, der jeweils anderen Phase als Dispergens. Dabei ist dann die kontinuierliche Phase I bzw. II um den Volumenteil verringert, der als Dispergens in der jeweils anderen Phase verteilt ist. Besonders bevorzugt sind hierbei Mittel, in denen Phase I in Mengen von 0,1 bis 25 Vol.-%, bevorzugt 0,2 bis 15 Vol.-%, bezogen auf das Volumen der Phase II, in Phase II emulgiert ist.In a further preferred embodiment of the invention, one or both of the continuous phases I and II parts, preferably 0.1 to 25 vol .-%, in particular 0.2 to 15 vol .-%, based on the volume of the respective continuous phase, each phase other than dispersant. The continuous phase I or II is then around Volume part reduced, which is distributed as a dispersant in the other phase. Especially agents in which phase I in amounts of 0.1 to 25% by volume are preferred 0.2 to 15 vol .-%, based on the volume of phase II, is emulsified in phase II.
In einer weiterhin bevorzugten verwendbaren Ausführungsform der Erfindung liegt neben den kontinuierlichen Phasen I und II ein Teil der beiden Phasen als Emulsion einer der beiden Phasen in der anderen Phase vor, wobei diese Emulsion durch zwei scharfe Grenzflächen, eine obere und eine untere, gegenüber den nicht an der Emulsion beteiligten Teilen der Phasen I und II abgegrenzt ist.In a further preferred usable embodiment of the invention lies next to the continuous phases I and II part of the two phases as an emulsion of one of the two Phases in the other phase, this emulsion being separated by two sharp interfaces, an upper and a lower, compared to the parts of the Phases I and II are delimited.
Die erfindungsgemäß verwendbaren Mittel enthalten Phase I und Phase II in einem Volumenverhältnis von 90 : 10 bis 10 : 90, vorzugsweise 75 : 25 bis 25 : 75, insbesondere 65 : 35 bis 35 : 65.The agents which can be used according to the invention contain phase I and phase II in one Volume ratio of 90:10 to 10:90, preferably 75:25 to 25:75, in particular 65: 35 to 35: 65.
Die verwendbaren Reinigungsmittel enthalten eine oder mehrere hydrophobe Komponenten. Geeignete Hydrophobkomponenten sind beispielsweise Dialkylether mit gleichen oder verschiedenen C4- bis C14-Alkylresten, insbesondere Dioctylether; Kohlenwasserstoffe mit einem Siedebereich von 100 bis 300 °C, insbesondere 140 bis 280 °C, z.B. aliphatische Kohlenwasserstoffe mit einem Siedebereich von 145 bis 200 °C, Isoparaffine mit einem Siedebereich von 200 bis 260 °C; etherische Öle, insbesondere Limonen und das aus Kiefernwurzeln und -stubben extrahierte Pine Oil; und auch Mischungen dieser Hydrophobkomponenten, insbesondere Mischungen von zwei oder drei der genannten Hydrophobkomponenten. Bevorzugte Gemische von Hydrophobkomponenten sind Gemische von verschiedenen Dialkylethern, von Dialkylethern und Kohlenwasserstoffen, von Dialkylethern und etherischen Ölen, von Kohlenwasserstoffen und etherischen Ölen, von Dialkylethern und Kohlenwasserstoffen und etherischen Ölen und von diesen Gemischen. Die Mittel enthalten Hydrophobkomponenten in Mengen, bezogen auf die Zusammensetzung, von 0 bis 20 Gew.-%, vorzugsweise 0,1 bis 14 Gew.-%, insbesondere 0,5 bis 10 Gew.-%, äußerst bevorzugt 0,8 bis 7 Gew.-%.The cleaning agents that can be used contain one or more hydrophobic components. Suitable hydrophobic components are, for example, dialkyl ethers with identical or different C 4 -C 14 -alkyl radicals, in particular dioctyl ether; Hydrocarbons with a boiling range from 100 to 300 ° C, in particular 140 to 280 ° C, for example aliphatic hydrocarbons with a boiling range from 145 to 200 ° C, isoparaffins with a boiling range from 200 to 260 ° C; essential oils, in particular limonene and pine oil extracted from pine roots and stumps; and also mixtures of these hydrophobic components, in particular mixtures of two or three of the hydrophobic components mentioned. Preferred mixtures of hydrophobic components are mixtures of various dialkyl ethers, of dialkyl ethers and hydrocarbons, of dialkyl ethers and essential oils, of hydrocarbons and essential oils, of dialkyl ethers and hydrocarbons and essential oils and of these mixtures. The compositions contain hydrophobic components in amounts, based on the composition, of 0 to 20% by weight, preferably 0.1 to 14% by weight, in particular 0.5 to 10% by weight, most preferably 0.8 to 7 wt .-%.
Die erfindungsgemäß verwendbaren Mittel können Phasentrennhilfsmittel enthalten. Geeignete Phasentrennhilfsmittel sind beispielsweise die Alkalimetall- und Erdalkalimetallchloride und -sulfate, insbesondere Natrium- und Kaliumchlorid und -sulfat, sowie Ammoniumchlorid und -sulfat bzw. deren Mischungen. Die genannten Salze unterstützen als starke Elektrolyte die Phasentrennung durch den Salzeffekt. Auch Buildersalze bewirken als Elektrolyte diesen Effekt und eignen sich dementsprechend ebenfalls als Phasentrennhilfsmittel. Die Mittel enthalten Phasentrennhilfsmittel in Mengen, bezogen auf die Zusammensetzung, von 0 bis 30 Gew.-%, vorzugsweise 1 bis 20 Gew.-%, insbesondere 3 bis 15 Gew.-%, äußerst bevorzugt 5 bis 12 Gew.-%.The agents that can be used in accordance with the invention can contain phase separation aids. Suitable phase separation aids are, for example, the alkali metal and Alkaline earth metal chlorides and sulfates, especially sodium and potassium chloride and sulfate, and ammonium chloride and sulfate or mixtures thereof. The salts mentioned as strong electrolytes support phase separation through the salt effect. Also Builder salts act as electrolytes and are therefore suitable also as phase separation aid. The agents contain phase separation aids in quantities, based on the composition, from 0 to 30% by weight, preferably 1 to 20% by weight, in particular 3 to 15% by weight, most preferably 5 to 12% by weight.
Die erfindungsgemäß verwendeten Mittel können als Tensidkomponente anionische, nichtionische, amphotere oder kationische Tenside bzw. Tensidgemische aus einer, mehreren oder allen diesen Tensidklassen enthalten. Die Mittel enthalten Tenside in Mengen, bezogen auf die Zusammensetzung, von 0,01 bis 30 Gew.-%, vorzugsweise 0,1 bis 20 Gew.-%, insbesondere 1 bis 14 Gew.-%, äußerst bevorzugt 3 bis 10 Gew.-%.The agents used according to the invention can be anionic, non-ionic, amphoteric or cationic surfactants or surfactant mixtures of one or more or contain all of these classes of surfactants. The detergents contain surfactants in quantities on the composition, from 0.01 to 30% by weight, preferably 0.1 to 20% by weight, in particular 1 to 14% by weight, most preferably 3 to 10% by weight.
Geeignete Niotenside sind beispielsweise C8-C18-Alkylalkoholpolyglykolether, Alkylpolyglykoside sowie stickstoffhaltige Tenside bzw. Mischungen davon, insbesondere der ersten beiden. Die Mittel enthalten nichtionische Tenside in Mengen, bezogen auf die Zusammensetzung, von 0 bis 30 Gew.-%, vorzugsweise 0,1 bis 20 Gew.-%, insbesondere 0,5 bis 14 Gew.-%, äußerst bevorzugt 1 bis 10 Gew.-%. Suitable nonionic surfactants are, for example, C 8 -C 18 alkyl alcohol polyglycol ethers, alkyl polyglycosides and nitrogen-containing surfactants or mixtures thereof, in particular the first two. The compositions contain nonionic surfactants in amounts, based on the composition, of 0 to 30% by weight, preferably 0.1 to 20% by weight, in particular 0.5 to 14% by weight, extremely preferably 1 to 10% by weight .-%.
C8-C18-Alkylalkoholpolypropylenglykol/polyethylenglykolether stellen bevorzugte bekannte
nichtionische Tenside dar. Sie können durch die Formel II,
RiO-(CH2CH(CH3)O) p (CH2CH2O) e -H, beschrieben werden, in der Ri für einen linearen oder
verzweigten, aliphatischen Alkyl- und/oder Alkenylrest mit 8 bis 18 Kohlenstoffatomen, p für
0 oder Zahlen von 1 bis 3 und e für Zahlen von 1 bis 20 steht.
Die C8-C18-Alkylalkoholpolyglykolether der Formel II kann man durch Anlagerung von
Propylenoxid und/oder Ethylenoxid an Alkylalkohole, vorzugsweise an Fettalkohole,
erhalten. Typische Beispiele sind Polyglykolether der Formel II, in der Ri für einen Alkylrest
mit 8 bis 18 Kohlenstoffatomen, p für 0 bis 2 und e für Zahlen von 2 bis 7 steht. Bevorzugte
Vertreter sind beispielsweise C10-C14-Fettalkohol+1PO+6EO-ether (p = 1, e = 6) und C12-C18-Fettalkohol+7EO-ether
(p = 0, e = 7) sowie deren Mischungen.
Es können auch endgruppenverschlossene C8-C18-Alkylalkoholpolyglykolether eingesetzt
werden, d.h. Verbindungen in denen die freie OH-Gruppe in der Formel II verethert ist. Die
endgruppenverschlossenen C8-C18-Alkylalkoholpolyglykolether können nach einschlägigen
Methoden der präparativen organischen Chemie erhalten werden. Vorzugsweise werden C8-C18-Alkylalkohopolyglykolether
in Gegenwart von Basen mit Alkylhalogeniden, insbesondere
Butyl- oder Benzylchlorid, umgesetzt. Typische Beispiele sind Mischether der
Formel II, in der Ri für einen technischen Fettalkoholrest, vorzugsweise C12/14-Kokosalkylrest,
p für 0 und e für 5 bis 10 stehen, die mit einer Butylgruppe verschlossen sind.C 8 -C 18 alkyl alcohol polypropylene glycol / polyethylene glycol ethers are preferred known nonionic surfactants. They can be described by the formula II, R i O- (CH 2 CH (CH 3 ) O) p (CH 2 CH 2 O) e -H in which R i is a linear or branched, aliphatic alkyl and / or alkenyl radical having 8 to 18 carbon atoms, p is 0 or numbers from 1 to 3 and e is numbers from 1 to 20.
The C 8 -C 18 alkyl alcohol polyglycol ethers of the formula II can be obtained by addition of propylene oxide and / or ethylene oxide to alkyl alcohols, preferably to fatty alcohols. Typical examples are polyglycol ethers of the formula II in which R i is an alkyl radical having 8 to 18 carbon atoms, p is 0 to 2 and e is a number from 2 to 7. Preferred representatives are, for example, C 10 -C 14 fatty alcohol + 1PO + 6EO ether ( p = 1, e = 6) and C 12 -C 18 fatty alcohol + 7EO ether ( p = 0, e = 7) and mixtures thereof ,
End-capped C 8 -C 18 -alkyl alcohol polyglycol ethers can also be used, ie compounds in which the free OH group in the formula II is etherified. The end-capped C 8 -C 18 alkyl alcohol polyglycol ethers can be obtained by the relevant methods of preparative organic chemistry. C 8 -C 18 -Alkyl alcohol polyglycol ethers are preferably reacted in the presence of bases with alkyl halides, in particular butyl or benzyl chloride. Typical examples are mixed ethers of the formula II in which R i stands for an industrial fatty alcohol residue, preferably C 12/14 cocoalkyl residue, p for 0 and e for 5 to 10, which are sealed with a butyl group.
Bevorzugte nichtionische Tenside sind weiterhin Alkylpolyglykoside (APG) der Formel III, RiiO[G] x , in der Rii für einen linearen oder verzweigten, gesättigten oder ungesättigten Alkylrest mit 8 bis 22 Kohlenstoffatomen, [G] für einen glykosidisch verknüpften Zuckerrest und x für eine Zahl von 1 bis 10 stehen. APG sind nichtionische Tenside und stellen bekannte Stoffe dar, die nach den einschlägigen Verfahren der präparativen organischen Chemie erhalten werden können. Die Indexzahl x in der allgemeinen Formel III gibt den Oligomerisierungsgrad (DP-Grad) an, d.h. die Verteilung von Mono- und Oligoglykosiden, und steht für eine Zahl zwischen 1 und 10. Während x in einer gegebenen Verbindung stets ganzzahlig sein muß und hier vor allem die Werte x = 1 bis 6 annehmen kann, ist der Wert x für ein bestimmtes Alkylglykosid eine analytisch ermittelte rechnerische Größe, die meistens eine gebrochene Zahl darstellt. Vorzugsweise werden Alkylglykoside mit einem mittleren Oligomerisierungsgrad x von 1,1 bis 3,0 eingesetzt. Aus anwendungstechnischer Sicht sind solche Alkylglykoside bevorzugt, deren Oligomerisierungsgrad kleiner als 1,7 ist und insbesondere zwischen 1,2 und 1,6 liegt. Als glykosidische Zucker wird vorzugsweise Xylose, insbesondere aber Glucose verwendet. Der Alkyl- bzw. Alkenylrest Rii (Formel III) kann sich von primären Alkoholen mit 8 bis 18, vorzugsweise 8 bis 14 Kohlenstoffatomen ableiten. Typische Beispiele sind Capronalkohol, Caprylalkohol, Caprinalkohol und Undecylalkohol sowie deren technische Gemische, wie sie beispielsweise im Verlauf der Hydrierung von technischen Fettsäuremethylestern oder im Verlauf der Hydrierung von Aldehyden aus der ROELENschen Oxosynthese anfallen. Vorzugsweise leitet sich der Alkyl- bzw. Alkenylrest Rii aber von Laurylalkohol, Myristylalkohol, Cetylalkohol, Palmoleylalkohol, Stearylalkohol, Isostearylalkohol oder Oleylalkohol ab. Weiterhin sind Elaidylalkohol, Petroselinylalkohol, Arachidylalkohol, Gadoleylalkohol, Behenylalkohol, Erucylalkohol sowie deren technische Gemische zu nennen.Preferred nonionic surfactants are furthermore alkyl polyglycosides (APG) of the formula III, R ii O [G] x , in which R ii for a linear or branched, saturated or unsaturated alkyl radical having 8 to 22 carbon atoms, [G] for a glycosidically linked sugar radical and x stands for a number from 1 to 10. APG are non-ionic surfactants and are known substances that can be obtained using the relevant methods of preparative organic chemistry. The index number x in the general formula III indicates the degree of oligomerization (DP degree), ie the distribution of mono- and oligoglycosides, and stands for a number between 1 and 10. While x must always be an integer in a given compound and here before can assume all the values x = 1 to 6, the value x for a certain alkyl glycoside is an analytically determined arithmetic parameter, which usually represents a fractional number. Alkyl glycosides with an average degree of oligomerization x of 1.1 to 3.0 are preferably used. From an application point of view, those alkyl glycosides are preferred whose degree of oligomerization is less than 1.7 and in particular between 1.2 and 1.6. Xylose, but especially glucose, is preferably used as the glycosidic sugar. The alkyl or alkenyl radical R ii (formula III) can be derived from primary alcohols having 8 to 18, preferably 8 to 14, carbon atoms. Typical examples are capronic alcohol, caprylic alcohol, capric alcohol and undecyl alcohol and their technical mixtures, such as those obtained in the course of the hydrogenation of technical fatty acid methyl esters or in the course of the hydrogenation of aldehydes from ROELEN's oxosynthesis. However, the alkyl or alkenyl radical R ii is preferably derived from lauryl alcohol, myristyl alcohol, cetyl alcohol, palmoleyl alcohol, stearyl alcohol, isostearyl alcohol or oleyl alcohol. Elaidyl alcohol, petroselinyl alcohol, arachidyl alcohol, gadoleyl alcohol, behenyl alcohol, erucyl alcohol and their technical mixtures are also to be mentioned.
Als weitere nichtionische Tenside können stickstoffenthaltende Tenside enthalten sein, z.B. Fettsäurepolyhydroxyamide, beispielsweise Glucamide, und Ethoxylate von Alkylaminen, vicinalen Diolen und/oder Carbonsäureamiden, die Alkylgruppen mit 10 bis 22 C-Atomen, vorzugsweise 12 bis 18 C-Atomen, besitzen. Der Ethoxylierungsgrad dieser Verbindungen liegt dabei in der Regel zwischen 1 und 20, vorzugsweise zwischen 3 und 10. Bevorzugt sind Ethanolamid-Derivate von Alkansäuren mit 8 bis 22 C-Atomen, vorzugsweise 12 bis 16 C-Atomen. Zu den besonders geeigneten Verbindungen gehören die Laurinsäure-, Myristinsäure- und Palmitinsäuremonoethanolamide. Nitrogen-containing surfactants may be included as further nonionic surfactants, e.g. Fatty acid polyhydroxyamides, for example glucamides, and ethoxylates of alkylamines, vicinal diols and / or carboxamides, the alkyl groups with 10 to 22 carbon atoms, preferably have 12 to 18 carbon atoms. The degree of ethoxylation of these compounds is generally between 1 and 20, preferably between 3 and 10. Preferred Ethanolamide derivatives of alkanoic acids with 8 to 22 carbon atoms, preferably 12 to 16 carbon atoms. The particularly suitable compounds include the lauric acid, Myristic and palmitic monoethanolamides.
Geeignete Aniontenside sind die bevorzugten C8-C18-Alkylsulfate, C8-C18-Alkyletherulfate, d.h. die Sulfatierungsprodukte der Alkoholether der Formel II, und/oder C8-C18-Alkylbenzolsulfonate, aber auch C8-C18-Alkansulfonate, C8-C18-α-Olefinsulfonate,sulfonierte C8-C18-Fettsäuren, insbesondere Dodecylbenzolsulfonat, C8-C22-Carbonsäureamidethersulfate, Sulfonbernsteinsäuremono- und -di-C1-C12-Alkylester, C8-C18-Alkylpolyglykolethercarboxylate, C8-C18-N-Acyltauride, C8-C18-N-Sarkosinate und C8-C18-Alkylisethionate bzw. deren Mischungen. Sie werden in Form ihrer Alkalimetall- und Erdalkalimetallsalze, insbesondere Natrium-, Kalium- und Magnesiumsalze, wie auch Ammonium- und Mono-, Di-, Tri- bzw. Tetraalkylammoniumsalze sowie im Falle der Sulfonate auch in Form ihrer korrespondierende Säure, z.B. Dodecylbenzolsulfonsäure, eingesetzt. Die Mittel enthalten anionische Tenside in Mengen, bezogen auf die Zusammensetzung, von 0 bis 30 Gew.-%, vorzugsweise 0,1 bis 20 Gew.-%, insbesondere 1 bis 14 Gew.-%, äußerst bevorzugt 2 bis 10 Gew.-%.Suitable anionic surfactants are the preferred C 8 -C 18 alkyl sulfates, C 8 -C 18 alkyl ether sulfates, ie the sulfation products of the alcohol ethers of the formula II, and / or C 8 -C 18 alkyl benzene sulfonates, but also C 8 -C 18 alkanesulfonates , C 8 -C 18 -α-olefin sulfonates, sulfonated C 8 -C 18 fatty acids, especially dodecylbenzenesulfonate, C 8 -C 22 carboxamide amide ether sulfates, sulfonic succinic acid mono- and di-C 1 -C 12 alkyl esters, C 8 -C 18 -Alkylpolyglykolethercarboxylate, C 8 -C 18 -N-acyl taurides, C 8 -C 18 -N-sarcosinates and C 8 -C 18 -alkyl isethionates or mixtures thereof. They are in the form of their alkali metal and alkaline earth metal salts, in particular sodium, potassium and magnesium salts, as well as ammonium and mono-, di-, tri- or tetraalkylammonium salts and, in the case of the sulfonates, also in the form of their corresponding acid, for example dodecylbenzenesulfonic acid, used. The compositions contain anionic surfactants in amounts, based on the composition, of 0 to 30% by weight, preferably 0.1 to 20% by weight, in particular 1 to 14% by weight, extremely preferably 2 to 10% by weight. %.
Wegen ihrer schaumdämpfenden Eigenschaften können die erfindungsgemäßen Mittel auch Seifen, d.h. Alkali- oder Ammoniumsalze gesättigter oder ungesättigter C6-C22-Fettsäuren, enthalten. Die Seifen können in einer Menge bis zu 5 Gew.-%, vorzugsweise von 0,1 bis 2 Gew.-%, eingesetzt werden.Because of their foam-suppressing properties, the agents according to the invention can also contain soaps, ie alkali metal or ammonium salts of saturated or unsaturated C 6 -C 22 fatty acids. The soaps can be used in an amount of up to 5% by weight, preferably from 0.1 to 2% by weight.
Geeignete Amphotenside sind beispielsweise Betaine der Formel (Riii)(Riv)(Rv)N+CH2COO-, in der Riii einen gegebenenfalls durch Heteroatome oder Heteroatomgruppen unterbrochenen Alkylrest mit 8 bis 25, vorzugsweise 10 bis 21 Kohlenstoffatomen und Riv sowie Rv gleichartige oder verschiedene Alkylreste mit 1 bis 3 Kohlenstoffatomen bedeuten, insbesondere C10-C18-Alkyl-dimethylcarboxymethylbetain und C11-C17-Alkylamidopropyldimethylcarboxymethylbetain. Die Mittel enthalten amphotere Tenside in Mengen, bezogen auf die Zusammensetzung, von 0 bis 15 Gew.-%, vorzugsweise 0,01 bis 10 Gew.-%, insbesondere 0,1 bis 5 Gew.-%. Suitable amphoteric surfactants are, for example, betaines of the formula (R iii ) (R iv ) (R v ) N + CH 2 COO - , in which R iii is an alkyl radical with 8 to 25, preferably 10 to 21, carbon atoms and R, which is optionally interrupted by heteroatoms or heteroatom groups iv and R v are identical or different alkyl radicals having 1 to 3 carbon atoms, in particular C 10 -C 18 -alkyldimethylcarboxymethylbetaine and C 11 -C 17 -alkylamidopropyldimethylcarboxymethylbetaine. The compositions contain amphoteric surfactants in amounts, based on the composition, of 0 to 15% by weight, preferably 0.01 to 10% by weight, in particular 0.1 to 5% by weight.
Geeignete Kationtenside sind u.a. die quartären Ammoniumverbindungen der Formel (Rvi)(Rvii)(Rviii)(Rix)N+ X-, in der Rvi bis Rix für vier gleich- oder verschiedenartige, insbesondere zwei lang- und zwei kurzkettige, Alkylreste und X- für ein Anion, insbesondere ein Halogenidion, stehen, beispielsweise Didecyl-dimethyl-ammoniumchlorid, Alkyl-benzyldidecyl-ammoniumchlorid und deren Mischungen. Die Mittel enthalten kationische Tenside in Mengen, bezogen auf die Zusammensetzung, von 0 bis 10 Gew.-%, vorzugsweise 0,01 bis 5 Gew.-%, insbesondere 0,1 bis 3 Gew.-%.Suitable cationic surfactants include the quaternary ammonium compounds of the formula (R vi ) (R vii ) (R viii ) (R ix ) N + X - , in which R vi to R ix for four identical or different types, in particular two long and two short-chain, alkyl radicals and X - represent an anion, in particular a halide ion, for example didecyldimethylammonium chloride, alkylbenzyldidecylammonium chloride and mixtures thereof. The compositions contain cationic surfactants in amounts, based on the composition, of 0 to 10% by weight, preferably 0.01 to 5% by weight, in particular 0.1 to 3% by weight.
In einer bevorzugten Ausführungsform enthalten die erfindungsgemäßen Mittel anionische und nichtionische Tenside nebeneinander, vorzugsweise C8-C18-Alkylbenzolsulfonate, C8-C18-Alkylsulfate und/oder C8-C18-Alkylethersulfate neben C8-C18-Alkylalkoholpolyglykolethern und/oder Alkylpolyglykosiden, insbesondere C8-C18-Alkylbenzolsulfonate neben C8-C18-Alkylalkoholpolyglykolethern.In a preferred embodiment, the agents according to the invention contain anionic and nonionic surfactants next to one another, preferably C 8 -C 18 alkylbenzenesulfonates, C 8 -C 18 alkyl sulfates and / or C 8 -C 18 alkyl ether sulfates in addition to C 8 -C 18 alkyl alcohol polyglycol ethers and / or alkyl polyglycosides, in particular C 8 -C 18 alkylbenzenesulfonates in addition to C 8 -C 18 alkyl alcohol polyglycol ethers.
Weiterhin können die erfindungsgemäßen Mittel Builder enthalten. Geeignete Builder sind beispielsweise Alkalimetallgluconate, -citrate, -nitrilotriacetate, -carbonate und -bicarbonate, insbesondere Natriumgluconat, -citrat und -nitrilotriacetat sowie Natrium- und Kaliumcarbonat und -bicarbonat, sowie Alkalimetall- und Erdalkalimetallhydroxide, insbesondere Natrium- und Kaliumhydroxid, Ammoniak und Amine, insbesondere Monound Triethanolamin, bzw. deren Mischungen. Hierzu zählen auch die Salze der Glutarsäure, Bernsteinsäure, Adipinsäure, Weinsäure und Benzolhexacarbonsäure sowie Phosphonate und Phosphate. Die Mittel enthalten Builder in Mengen, bezogen auf die Zusammensetzung, von 0 bis 20 Gew.-%, vorzugsweise 0,01 bis 12 Gew.-%, insbesondere 0,1 bis 8 Gew.-%, äußerst bevorzugt 0,3 bis 5 Gew.-%, wobei jedoch die Menge an Natriumhexametaphosphat ― ausgenommen die verwendungsgemäßen Mittel ― auf 0 bis 5 Gew.-% beschränkt ist. Als Elektrolyte sind die Buildersalze zugleich Phasentrennhilfsmittel. The agents according to the invention can also contain builders. Suitable builders are for example alkali metal gluconates, citrates, nitrilotriacetates, carbonates and bicarbonates, in particular sodium gluconate, citrate and nitrilotriacetate as well as sodium and Potassium carbonate and bicarbonate, as well as alkali metal and alkaline earth metal hydroxides, especially sodium and potassium hydroxide, ammonia and amines, especially monound Triethanolamine, or their mixtures. This also includes the salts of glutaric acid, Succinic acid, adipic acid, tartaric acid and benzene hexacarboxylic acid as well as phosphonates and Phosphates. The agents contain builders in amounts, based on the composition, of 0 to 20% by weight, preferably 0.01 to 12% by weight, in particular 0.1 to 8% by weight, extremely preferably 0.3 to 5% by weight, but the amount of sodium hexametaphosphate except for the agents used - is limited to 0 to 5 wt .-%. As Electrolytes are the builder salts at the same time phase separation aids.
Neben den genannten Komponenten können die erfindungsgemäßen Mittel weitere Hilfs- und Zusatzstoffe enthalten, wie sie in derartigen Mitteln üblich sind. Hierzu zählen insbesondere Polymere, Soil-Release-Wirkstoffe, Lösungsmittel (z.B. Ethanol, Isopropanol, Glykolether), Lösungsvermittler, Hydrotrope (z.B. Cumolsulfonat, Octylsulfat, Butylglucosid, Butylglykol), Reinigungsverstärker, Viskositätsregler (z.B. synthetische Polymere wie Polysaccharide, Polyacrylate, in der Natur vorkommenden Polymere und deren Derivate wie Xanthangum, weitere Polysaccharide und/oder Gelatine), pH-Regulatoren (z.B. Citronensäure, Alkanolamine oder NaOH), Desinfektionsmittel, Antistatika, Konservierungsmittel, Bleichsysteme, Enzyme, Parfüm, Farb- und Duftstoffe sowie Trübungsmittel oder auch Hautschutzmittel, wie sie in EP-A-522 556 beschrieben sind. Die Menge an derartigen Zusätzen liegt üblicherweise nicht über 12 Gew.-% im Reinigungsmittel. Die Untergrenze des Einsatzes hängt von der Art des Zusatzstoffes ab und kann beispielsweise bei Farbstoffen bis zu 0,001 Gew.-% und darunter betragen. Vorzugsweise liegt die Menge an Hilfsstoffen zwischen 0,01 und 7 Gew.-%, insbesondere 0,1 und 4 Gew.-%.In addition to the components mentioned, the agents according to the invention can contain further auxiliaries and additives as are customary in such agents. These include in particular polymers, soil release agents, solvents (e.g. ethanol, isopropanol, glycol ether), solubilizers, hydrotropes (e.g. cumene sulfonate, octyl sulfate, butyl glucoside, butyl glycol), cleaning enhancers, viscosity regulators (e.g. synthetic polymers such as polysaccharides, polyacrylates, in nature occurring polymers and their derivatives such as xanthan gum, other polysaccharides and / or gelatin), pH regulators (e.g. citric acid, alkanolamines or NaOH), disinfectants, antistatic agents, preservatives, bleaching systems, enzymes, perfume, colors and fragrances as well as opacifiers or skin protection agents, as described in EP-A-522 556 . The amount of such additives is usually not more than 12% by weight in the cleaning agent. The lower limit of use depends on the type of additive and can be up to 0.001% by weight and below, for example, for dyes. The amount of auxiliaries is preferably between 0.01 and 7% by weight, in particular 0.1 and 4% by weight.
Der pH-Wert der erfindungsgemäßen Mittel kann über einen weiten Bereich variiert werden, bevorzugt ist jedoch ein Bereich von 2,5 bis 12, insbesondere 5 bis 10,5. Unter dem pH-Wert der erfindungsgemäßen Mittel ist im Rahmen der vorliegenden Erfindung der pH-Wert des Mittels in Form der temporären Emulsion zu verstehen.The pH of the agents according to the invention can be varied over a wide range, but a range from 2.5 to 12, in particular 5 to 10.5, is preferred. In the context of the present invention, the pH of the agents according to the invention is understood to mean the pH of the agent in the form of the temporary emulsion.
Die erfindungsgemäßen Mittel können durch Aufmischen unmittelbar aus ihren Rohstoffen, anschließendes Durchmischen und abschließendes Stehen des Mittels zur Auftrennung der temporären Emulsion hergestellt werden. The agents according to the invention can be mixed directly from their raw materials, then mixing and finally standing the means for separating the temporary emulsion.
Die erfindungsgemäßen Mittel E1 bis E7 wurden wie zuvor beschrieben hergestellt. Ihre
Zusammensetzungen in Gew.-% und ihr pH-Wert sind in Tabelle 1 wiedergegeben. Die
Mittel zeigen zwei kontinuierliche Phasen, wobei die obere leicht milchig trüb ist und bilden
beim Schütteln temporär eine cremig aussehende Emulsion.
Als Komponenten wurden eingesetzt
The components were used
Zur Prüfung des Reinigungsvermögens der erfindungsgemäß formulierten Reiniger-Zusammensetzungen diente die unten nach Seifen-Öle-Fette-Wachse 1986, 112, S. 371, beschriebene Testmethode, die sehr gut reproduzierbare Ergebnisse liefert. Danach wurde das zu prüfende Reinigungsmittel auf eine künstlich angeschmutzte weiße Kunststoffoberfläche gegeben. Als künstliche Anschmutzung für die verdünnte Anwendung des Reinigungsmittels wurde ein Gemisch aus Ruß, Maschinenöl, Triglycerid aus gesättigten Fettsäuren und niedersiedendem aliphatischen Kohlenwasserstoff verwendet. Die Testfläche von 26 x 28 cm wurde mit Hilfe eines Flächenstreichers gleichmäßig mit 2 g der künstlichen Anschmutzung beschichtet.The test method described below according to Seifen-Öle-Fette-Wachsen 1986 , 112 , p. 371, which provides very reproducible results, was used to test the cleaning ability of the cleaner compositions formulated according to the invention. The cleaning agent to be tested was then placed on an artificially soiled white plastic surface. A mixture of carbon black, machine oil, triglyceride of saturated fatty acids and low-boiling aliphatic hydrocarbon was used as artificial soiling for the dilute use of the cleaning agent. The test area of 26 x 28 cm was evenly coated with 2 g of the artificial soiling with the aid of a surface coater.
Ein Kunststoffschwamm wurde jeweils mit 10 ml der zu prüfenden Reinigungsmittellösung getränkt und mechanisch auf der ebenfalls mit 10 ml der zu prüfenden Reinigungsmittel beschichteten Testfläche bewegt. Nach 10 Wischbewegungen wurde die gereinigte Testfläche unter fließendes Wasser gehalten und der lose sitzende Schmutz entfernt. Die Reinigungswirkung, d.h. der Weißgrad der sogenannten Kunststoffoberfläche wurde mit einem Farb-Differenz-Meßgerät "Microcolor" (Dr. Lange) gemessen. Als Weiß-Standard diente die saubere unbehandelte weiße Kunststoffoberfläche.A plastic sponge was each with 10 ml of the detergent solution to be tested impregnated and mechanically on the detergent also to be tested with 10 ml coated test surface moves. After 10 wiping movements, the cleaned test area Held under running water and the loose dirt removed. The cleaning effect, i.e. the whiteness of the so-called plastic surface was measured with a Color difference measuring device "Microcolor" (Dr. Lange) measured. The served as the white standard clean untreated white plastic surface.
Der Test wurde mit dem erfindungsgemäßen Reinigungsmittel E1 in verdünnter Anwendung mit einer Konzentration von 6 ml·l-1 und in unverdünnter Anwendung durchgeführt. Zum Vergleich wurde der Test mit einem im deutschen Markt führenden Allzweckreiniger mit mehr als 10 Gew.-% Tensiden (V1) in verdünnter Anwendung von ebenfalls 6 ml·l-1 sowie in unverdünnter Anwendung durchgeführt. The test was carried out with the inventive cleaning agent E1 in diluted usage at a concentration of 6 MLL -1 and in undiluted. For comparison, the test was carried out with a leading all-purpose cleaner in the German market with more than 10% by weight of surfactants ( V1 ) in dilute application of 6 ml·l -1 as well as in undiluted application.
Das erfindungsgemäße Mittel E1 übertrifft in seiner Reinigungsleistung hierbei den deutlich tensidreicheren Reiniger V1 sowohl in der verdünnten Anwendung wie auch in der unverdünnten Anwendung.The inventive cleaning agent E1 outperforms the significantly more surfactant-rich cleaner V1 in both the diluted application and in the undiluted application.
Das Rückstandsverhalten wurde auf schwarzen Kacheln geprüft. Die Rückstandsnote der erfindungsgemäßen Mittel liegt hierbei auf dem Niveau der handelsüblichen Allzweckreiniger in Deutschland. Das ist auch dann noch der Fall, wenn die Mittel Hydrophobkomponenten enthalten. The residue behavior was checked on black tiles. The backlog of the The agent according to the invention is at the level of commercially available all-purpose cleaners in Germany. This is still the case even if the agent contains hydrophobic components contain.
Die Zusammensetzung der Phasen I und II des erfindungsgemäßen Reinigungsmittels E1 ist
in Tabelle 2 angegeben.
Die obere Phase II beinhaltet fast die gesamte Menge an Tensid (a, c), Hydrophobkomponente (j) und Parfüm (k), während die untere Phase I fast ausschließlich einen Teil des Phasentrennhilfsmittels (f) und des Builders (d) enthält.The upper phase II contains almost the entire amount of surfactant (a, c), hydrophobic component (j) and perfume (k), while the lower phase I almost exclusively a part of the Phase separation aid (f) and the builder (d) contains.
Claims (14)
- Use of an aqueous liquid multiphase surfactant-containing cleaner having at least two continuous phases, which has at least one lower aqueous phase I and an upper aqueous phase II which is immiscible with the first phase, and which can be temporarily converted into an emulsion by shaking, for the cleaning of hard surfaces, where the commposition has one or more hydrophobic components.
- Use of a composition according to Claim 1, characterized in that it comprises from 0 to 5% by weight of sodium hexametaphosphate.
- Use of a composition according to either of Claims 1 and 2, characterized in that the continuous phases I and II are delimited from one another by a sharp interface.
- Use of a composition according to one of Claims 1 to 3, characterized in that one or both of the continuous phases I and II comprise parts, preferably from 0.1 to 25% by volume, in particular from 0.2 to 15% by volume, based on the volume of the respective continuous phase, of the other phase in each case as dispersant.
- Use of a composition according to one of Claims 1 to 4, characterized in that phase I is emulsified in phase II in amounts of from 0.1 to 25% by volume, preferably from 0.2 to 15% by volume, based on the volume of phase II.
- Use of a composition according to one of Claims 1 to 5, characterized in that, in addition to the continuous phases I and II, part of the two phases is in the form of an emulsion of one of the two phases in the other phase, this emulsion being delimited by two sharp interfaces, one upper and one lower, from the parts of phases I and II not involved in the emulsion.
- Use of a composition according to one of Claims 1 to 6, characterized in that the composition comprises phase I and phase II in a volume ratio from 90:10 to 10:90, preferably from 75:25 to 25:75, in particular from 65:35 to 35:65.
- Use of a composition according to one of Claims 1 to 7, characterized in that the composition additionally comprises hydrophobic components from the group of dialkyl ethers having identical or different C4- to C14-alkyl radicals, in particular dioctyl ethers, hydrocarbons having a boiling range from 100 to 300°C, in particular from 140 to 280°C, ethereal oils, in particular limonene and pine oil, and mixtures thereof, in particular mixtures of two or three of said hydrophobic components.
- Use of a composition according to one of Claims 1 to 8, characterized in that the composition additionally comprises phase separation auxiliaries, preferably from the group of alkali metal and alkaline earth metal chlorides and sulphates, in particular sodium and potassium chloride and sulphate, and ammonium chloride and sulphate and mixtures thereof.
- Use of a composition according to one of Claims 1 to 9, characterized in that the composition comprises anionic surfactant, preferably from the group of C8-C18-alkyl sulphates, of C8-C18-alkyl ether sulphates and C8-C18-alkylbenzenesulphonates and mixtures thereof.
- Use of a composition according to one of Claims 1 to 10, characterized in that the composition comprises nonionic surfactant, preferably from the group of C8-C18-alkyl alcohol polyglycol ethers, of alkyl polyglycosides and mixtures thereof.
- Use of a composition according to one of Claims 1 to 11, characterized in that the composition comprises anionic and nonionic surfactant, preferably C8-C18-alkylbenzenesulphonates, C8-C18-alkyl sulphates and/or C8-C18-alkyl ether sulphates in addition to C8-C18-alkyl alcohol polyglycol ethers and/or alkyl polyglycosides, in particular C8-C18-alkylbenzene-sulphonates in addition to C8-C18-alkyl alcohol polyglycol ethers.
- Use of a composition according to one of Claims 1 to 12, characterized in that the composition comprises one or more cationic surfactants.
- Use of a composition according to one of Claims 1 to 13, characterized in that the composition additionally comprises builders, preferably from the group of alkali metal gluconates, citrates, nitrilotriacetates, carbonates and bicarbonates, and alkali metal and alkaline earth metal hydroxides, ammonia and amines, in particular mono- and triethanolamine, and mixtures thereof.
Applications Claiming Priority (5)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| DE19811386 | 1998-03-16 | ||
| DE19811386A DE19811386A1 (en) | 1998-03-16 | 1998-03-16 | Aqueous multiphase detergent forming temporary emulsion on shaking and used on hard surfaces |
| DE19859774 | 1998-12-23 | ||
| DE1998159774 DE19859774A1 (en) | 1998-12-23 | 1998-12-23 | Aqueous multiphase detergent |
| EP99911758A EP1064349B1 (en) | 1998-03-16 | 1999-03-09 | Aqueous multiphase detergents |
Related Parent Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| EP99911758A Division EP1064349B1 (en) | 1998-03-16 | 1999-03-09 | Aqueous multiphase detergents |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| EP1126019A1 EP1126019A1 (en) | 2001-08-22 |
| EP1126019B1 true EP1126019B1 (en) | 2003-06-04 |
Family
ID=26044653
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| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| EP99911758A Expired - Lifetime EP1064349B1 (en) | 1998-03-16 | 1999-03-09 | Aqueous multiphase detergents |
| EP01103811A Revoked EP1126019B1 (en) | 1998-03-16 | 1999-03-09 | Use of an aqueous multiphase cleaning agent for cleaning hard surfaces |
Family Applications Before (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| EP99911758A Expired - Lifetime EP1064349B1 (en) | 1998-03-16 | 1999-03-09 | Aqueous multiphase detergents |
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| US (1) | US6440924B1 (en) |
| EP (2) | EP1064349B1 (en) |
| JP (1) | JP2002506925A (en) |
| AT (2) | ATE242313T1 (en) |
| CA (1) | CA2324075A1 (en) |
| DE (2) | DE59905562D1 (en) |
| ES (2) | ES2200994T3 (en) |
| WO (1) | WO1999047635A2 (en) |
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| DE19936727A1 (en) | 1999-08-06 | 2001-02-08 | Henkel Kgaa | Nonionic surfactant based aqueous multiphase detergent |
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| DE19951635A1 (en) * | 1999-10-26 | 2001-05-17 | Henkel Kgaa | Aqueous multiphase detergent |
| DE10012949A1 (en) | 2000-03-16 | 2001-09-27 | Henkel Kgaa | Mixtures of cyclic and linear silicic esters of lower alcohols and fragrance and/or biocide alcohols are used as fragrance and/or biocide in liquid or solid laundry and other detergents and in skin and hair cosmetics |
| US6593283B2 (en) * | 2000-04-28 | 2003-07-15 | Ecolab Inc. | Antimicrobial composition |
| MXPA02012888A (en) | 2000-06-20 | 2003-05-14 | Procter & Gamble | Multi-phase fabric care composition for delivering multiple fabric care benefits. |
| US6475973B1 (en) * | 2000-07-07 | 2002-11-05 | Colgate-Palmolive Corp | Dual phase cleaning composition |
| DE10060096A1 (en) * | 2000-12-02 | 2002-07-04 | Henkel Kgaa | Multi-phase washing and cleaning agent with bleach |
| DE10137047A1 (en) * | 2001-07-31 | 2003-02-27 | Henkel Kgaa | Sprayable cleaner containing a droplet-shaped apolar component |
| US6521581B1 (en) | 2001-12-14 | 2003-02-18 | Unilever Home & Personal Care Usa, Division Of Conopco, Inc. | Water-soluble package with multiple distinctly colored layers of liquid laundry detergent |
| US6797685B2 (en) | 2002-04-26 | 2004-09-28 | Unilever Home & Personal Care Usa, Division Of Conopco, Inc. | Liquid laundry detergent with emulsion layer |
| US7448556B2 (en) | 2002-08-16 | 2008-11-11 | Henkel Kgaa | Dispenser bottle for at least two active fluids |
| GB2392166A (en) * | 2002-08-22 | 2004-02-25 | Reckitt Benckiser Inc | Composition separable into two phases |
| US20050075265A1 (en) * | 2003-09-12 | 2005-04-07 | L'oreal | Two-phase compositions and uses thereof |
| US7939485B2 (en) * | 2004-11-01 | 2011-05-10 | The Procter & Gamble Company | Benefit agent delivery system comprising ionic liquid |
| US20060090777A1 (en) * | 2004-11-01 | 2006-05-04 | Hecht Stacie E | Multiphase cleaning compositions having ionic liquid phase |
| US20060122088A1 (en) * | 2004-12-03 | 2006-06-08 | Sadlowski Eugene S | Unit dose two-layer liquid detergent packages |
| GB0524009D0 (en) * | 2005-11-25 | 2006-01-04 | Reckitt Benckiser Nv | Composition and method |
| DE102005061726A1 (en) * | 2005-12-21 | 2007-07-05 | Henkel Kgaa | Multiphase surfactant-containing detergents or rinsing agents have a vertical phase boundary especially to allow incompatible ingredients to be incorporated |
| DE102006011087A1 (en) * | 2006-03-08 | 2007-09-13 | Henkel Kgaa | Silicon-based active substance carriers containing aminoalkyl groups |
| DE102006013104A1 (en) * | 2006-03-20 | 2007-09-27 | Henkel Kgaa | Multi-phase washing, rinsing or cleaning agent with vertical phase boundaries |
| ITCR20060016A1 (en) * | 2006-06-07 | 2007-12-08 | Silvia Palladini | DETERGENT FORMULATIONS AT LOW ENVIRONMENTAL IMPACT |
| FR2917094B1 (en) * | 2007-06-08 | 2011-05-06 | Dalta | COMPOSITION FOR IMPREGNATION IN WIPES FOR CLEANING AND / OR CONTAMINATED SURFACE LUSTERING |
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| US9410111B2 (en) | 2008-02-21 | 2016-08-09 | S.C. Johnson & Son, Inc. | Cleaning composition that provides residual benefits |
| US8993502B2 (en) | 2008-02-21 | 2015-03-31 | S. C. Johnson & Son, Inc. | Cleaning composition having high self-adhesion to a vertical hard surface and providing residual benefits |
| US9481854B2 (en) | 2008-02-21 | 2016-11-01 | S. C. Johnson & Son, Inc. | Cleaning composition that provides residual benefits |
| ES2422261T5 (en) * | 2008-02-21 | 2017-05-12 | S.C. Johnson & Son, Inc. | Cleaning composition that has high self-adhesion and provides residual benefits |
| US8143206B2 (en) * | 2008-02-21 | 2012-03-27 | S.C. Johnson & Son, Inc. | Cleaning composition having high self-adhesion and providing residual benefits |
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| EP4050088A1 (en) | 2021-02-26 | 2022-08-31 | The Procter & Gamble Company | Liquid hand dishwashing detergent composition |
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1999
- 1999-03-09 ES ES01103811T patent/ES2200994T3/en not_active Expired - Lifetime
- 1999-03-09 JP JP2000536818A patent/JP2002506925A/en not_active Ceased
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- 1999-03-09 EP EP99911758A patent/EP1064349B1/en not_active Expired - Lifetime
- 1999-03-09 EP EP01103811A patent/EP1126019B1/en not_active Revoked
- 1999-03-09 WO PCT/EP1999/001507 patent/WO1999047635A2/en active IP Right Grant
- 1999-03-09 CA CA002324075A patent/CA2324075A1/en not_active Abandoned
- 1999-03-09 US US09/646,320 patent/US6440924B1/en not_active Expired - Fee Related
- 1999-03-09 DE DE59905562T patent/DE59905562D1/en not_active Expired - Lifetime
- 1999-03-09 ES ES99911758T patent/ES2200511T3/en not_active Expired - Lifetime
- 1999-03-09 DE DE59905877T patent/DE59905877D1/en not_active Revoked
- 1999-03-09 AT AT99911758T patent/ATE240387T1/en not_active IP Right Cessation
Also Published As
| Publication number | Publication date |
|---|---|
| DE59905562D1 (en) | 2003-06-18 |
| EP1064349A2 (en) | 2001-01-03 |
| EP1126019A1 (en) | 2001-08-22 |
| ES2200511T3 (en) | 2004-03-01 |
| US6440924B1 (en) | 2002-08-27 |
| DE59905877D1 (en) | 2003-07-10 |
| ATE242313T1 (en) | 2003-06-15 |
| EP1064349B1 (en) | 2003-05-14 |
| ES2200994T3 (en) | 2004-03-16 |
| WO1999047635A2 (en) | 1999-09-23 |
| ATE240387T1 (en) | 2003-05-15 |
| CA2324075A1 (en) | 1999-09-23 |
| WO1999047635A3 (en) | 2000-01-20 |
| JP2002506925A (en) | 2002-03-05 |
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