EP1400583A1 - Liquid washing and cleaning agents with viscosity modifying polymers - Google Patents
Liquid washing and cleaning agents with viscosity modifying polymers Download PDFInfo
- Publication number
- EP1400583A1 EP1400583A1 EP03018755A EP03018755A EP1400583A1 EP 1400583 A1 EP1400583 A1 EP 1400583A1 EP 03018755 A EP03018755 A EP 03018755A EP 03018755 A EP03018755 A EP 03018755A EP 1400583 A1 EP1400583 A1 EP 1400583A1
- Authority
- EP
- European Patent Office
- Prior art keywords
- cleaning
- acid
- disinfecting
- liquid washing
- bleaching agents
- 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.)
- Granted
Links
- 239000007788 liquid Substances 0.000 title claims abstract description 29
- 238000005406 washing Methods 0.000 title claims abstract description 19
- 239000012459 cleaning agent Substances 0.000 title claims description 16
- 229920000642 polymer Polymers 0.000 title description 26
- 238000004140 cleaning Methods 0.000 claims abstract description 28
- 229920001577 copolymer Polymers 0.000 claims abstract description 24
- 230000000249 desinfective effect Effects 0.000 claims abstract description 18
- 230000002209 hydrophobic effect Effects 0.000 claims abstract description 5
- 229920001281 polyalkylene Polymers 0.000 claims abstract description 3
- -1 cyclic N-vinylamides Chemical class 0.000 claims description 54
- 239000007844 bleaching agent Substances 0.000 claims description 17
- 239000000645 desinfectant Substances 0.000 claims description 17
- IAYPIBMASNFSPL-UHFFFAOYSA-N Ethylene oxide Chemical compound C1CO1 IAYPIBMASNFSPL-UHFFFAOYSA-N 0.000 claims description 13
- CERQOIWHTDAKMF-UHFFFAOYSA-M Methacrylate Chemical compound CC(=C)C([O-])=O CERQOIWHTDAKMF-UHFFFAOYSA-M 0.000 claims description 13
- NIXOWILDQLNWCW-UHFFFAOYSA-N 2-Propenoic acid Natural products OC(=O)C=C NIXOWILDQLNWCW-UHFFFAOYSA-N 0.000 claims description 12
- 150000001875 compounds Chemical class 0.000 claims description 10
- FWFUWXVFYKCSQA-UHFFFAOYSA-M sodium;2-methyl-2-(prop-2-enoylamino)propane-1-sulfonate Chemical compound [Na+].[O-]S(=O)(=O)CC(C)(C)NC(=O)C=C FWFUWXVFYKCSQA-UHFFFAOYSA-M 0.000 claims description 9
- PPBRXRYQALVLMV-UHFFFAOYSA-N Styrene Chemical compound C=CC1=CC=CC=C1 PPBRXRYQALVLMV-UHFFFAOYSA-N 0.000 claims description 8
- SMZOUWXMTYCWNB-UHFFFAOYSA-N 2-(2-methoxy-5-methylphenyl)ethanamine Chemical compound COC1=CC=C(C)C=C1CCN SMZOUWXMTYCWNB-UHFFFAOYSA-N 0.000 claims description 7
- GOOHAUXETOMSMM-UHFFFAOYSA-N Propylene oxide Chemical compound CC1CO1 GOOHAUXETOMSMM-UHFFFAOYSA-N 0.000 claims description 6
- 125000003438 dodecyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])* 0.000 claims description 6
- FQPSGWSUVKBHSU-UHFFFAOYSA-N methacrylamide Chemical compound CC(=C)C(N)=O FQPSGWSUVKBHSU-UHFFFAOYSA-N 0.000 claims description 6
- VZCYOOQTPOCHFL-UHFFFAOYSA-N trans-butenedioic acid Natural products OC(=O)C=CC(O)=O VZCYOOQTPOCHFL-UHFFFAOYSA-N 0.000 claims description 6
- 239000004215 Carbon black (E152) Substances 0.000 claims description 5
- CERQOIWHTDAKMF-UHFFFAOYSA-N Methacrylic acid Chemical compound CC(=C)C(O)=O CERQOIWHTDAKMF-UHFFFAOYSA-N 0.000 claims description 5
- OFOBLEOULBTSOW-UHFFFAOYSA-N Propanedioic acid Natural products OC(=O)CC(O)=O OFOBLEOULBTSOW-UHFFFAOYSA-N 0.000 claims description 5
- 125000001931 aliphatic group Chemical group 0.000 claims description 5
- 150000001412 amines Chemical class 0.000 claims description 5
- 125000003118 aryl group Chemical group 0.000 claims description 5
- VZCYOOQTPOCHFL-UPHRSURJSA-N maleic acid Chemical compound OC(=O)\C=C/C(O)=O VZCYOOQTPOCHFL-UPHRSURJSA-N 0.000 claims description 5
- 239000011976 maleic acid Substances 0.000 claims description 5
- XHZPRMZZQOIPDS-UHFFFAOYSA-N 2-Methyl-2-[(1-oxo-2-propenyl)amino]-1-propanesulfonic acid Chemical compound OS(=O)(=O)CC(C)(C)NC(=O)C=C XHZPRMZZQOIPDS-UHFFFAOYSA-N 0.000 claims description 4
- HRPVXLWXLXDGHG-UHFFFAOYSA-N Acrylamide Chemical compound NC(=O)C=C HRPVXLWXLXDGHG-UHFFFAOYSA-N 0.000 claims description 4
- NLHHRLWOUZZQLW-UHFFFAOYSA-N Acrylonitrile Chemical compound C=CC#N NLHHRLWOUZZQLW-UHFFFAOYSA-N 0.000 claims description 4
- KAKZBPTYRLMSJV-UHFFFAOYSA-N Butadiene Chemical compound C=CC=C KAKZBPTYRLMSJV-UHFFFAOYSA-N 0.000 claims description 4
- VQTUBCCKSQIDNK-UHFFFAOYSA-N Isobutene Chemical compound CC(C)=C VQTUBCCKSQIDNK-UHFFFAOYSA-N 0.000 claims description 4
- RRHGJUQNOFWUDK-UHFFFAOYSA-N Isoprene Chemical compound CC(=C)C=C RRHGJUQNOFWUDK-UHFFFAOYSA-N 0.000 claims description 4
- WHNWPMSKXPGLAX-UHFFFAOYSA-N N-Vinyl-2-pyrrolidone Chemical compound C=CN1CCCC1=O WHNWPMSKXPGLAX-UHFFFAOYSA-N 0.000 claims description 4
- XTXRWKRVRITETP-UHFFFAOYSA-N Vinyl acetate Chemical compound CC(=O)OC=C XTXRWKRVRITETP-UHFFFAOYSA-N 0.000 claims description 4
- PNLUGRYDUHRLOF-UHFFFAOYSA-N n-ethenyl-n-methylacetamide Chemical compound C=CN(C)C(C)=O PNLUGRYDUHRLOF-UHFFFAOYSA-N 0.000 claims description 4
- ZQXSMRAEXCEDJD-UHFFFAOYSA-N n-ethenylformamide Chemical compound C=CNC=O ZQXSMRAEXCEDJD-UHFFFAOYSA-N 0.000 claims description 4
- KDYFGRWQOYBRFD-UHFFFAOYSA-N succinic acid Chemical compound OC(=O)CCC(O)=O KDYFGRWQOYBRFD-UHFFFAOYSA-N 0.000 claims description 4
- 125000005131 dialkylammonium group Chemical group 0.000 claims description 3
- 125000005208 trialkylammonium group Chemical group 0.000 claims description 3
- 229920002818 (Hydroxyethyl)methacrylate Polymers 0.000 claims description 2
- JWYVGKFDLWWQJX-UHFFFAOYSA-N 1-ethenylazepan-2-one Chemical compound C=CN1CCCCCC1=O JWYVGKFDLWWQJX-UHFFFAOYSA-N 0.000 claims description 2
- BMCSBVHAGWUAQR-UHFFFAOYSA-N 2-hydroxy-2-(2-methylprop-2-enoylamino)acetic acid Chemical compound CC(=C)C(=O)NC(O)C(O)=O BMCSBVHAGWUAQR-UHFFFAOYSA-N 0.000 claims description 2
- KGIGUEBEKRSTEW-UHFFFAOYSA-N 2-vinylpyridine Chemical compound C=CC1=CC=CC=N1 KGIGUEBEKRSTEW-UHFFFAOYSA-N 0.000 claims description 2
- TYCHBDHDMFEQMC-UHFFFAOYSA-N 3-(dimethylamino)-2-methylprop-2-enoic acid Chemical compound CN(C)C=C(C)C(O)=O TYCHBDHDMFEQMC-UHFFFAOYSA-N 0.000 claims description 2
- UVRCNEIYXSRHNT-UHFFFAOYSA-N 3-ethylpent-2-enamide Chemical compound CCC(CC)=CC(N)=O UVRCNEIYXSRHNT-UHFFFAOYSA-N 0.000 claims description 2
- KFDVPJUYSDEJTH-UHFFFAOYSA-N 4-ethenylpyridine Chemical compound C=CC1=CC=NC=C1 KFDVPJUYSDEJTH-UHFFFAOYSA-N 0.000 claims description 2
- PBMWEQHOZPTUQQ-UHFFFAOYSA-N 4-hydroxy-2-methylbut-2-enamide Chemical compound NC(=O)C(C)=CCO PBMWEQHOZPTUQQ-UHFFFAOYSA-N 0.000 claims description 2
- IRLPACMLTUPBCL-KQYNXXCUSA-N 5'-adenylyl sulfate Chemical compound C1=NC=2C(N)=NC=NC=2N1[C@@H]1O[C@H](COP(O)(=O)OS(O)(=O)=O)[C@@H](O)[C@H]1O IRLPACMLTUPBCL-KQYNXXCUSA-N 0.000 claims description 2
- YSFGBPCBPNVLOK-UHFFFAOYSA-N 6-hydroxy-2-methylhex-2-enamide Chemical compound NC(=O)C(C)=CCCCO YSFGBPCBPNVLOK-UHFFFAOYSA-N 0.000 claims description 2
- LPQLVKHWWGULLA-UHFFFAOYSA-N C(C)(C)C(=CC(=O)N)C(C)C Chemical compound C(C)(C)C(=CC(=O)N)C(C)C LPQLVKHWWGULLA-UHFFFAOYSA-N 0.000 claims description 2
- WOBHKFSMXKNTIM-UHFFFAOYSA-N Hydroxyethyl methacrylate Chemical compound CC(=C)C(=O)OCCO WOBHKFSMXKNTIM-UHFFFAOYSA-N 0.000 claims description 2
- VVQNEPGJFQJSBK-UHFFFAOYSA-N Methyl methacrylate Chemical compound COC(=O)C(C)=C VVQNEPGJFQJSBK-UHFFFAOYSA-N 0.000 claims description 2
- 150000001408 amides Chemical class 0.000 claims description 2
- 150000001767 cationic compounds Chemical class 0.000 claims description 2
- 238000010276 construction Methods 0.000 claims description 2
- 125000006264 diethylaminomethyl group Chemical group [H]C([H])([H])C([H])([H])N(C([H])([H])*)C([H])([H])C([H])([H])[H] 0.000 claims description 2
- 125000004494 ethyl ester group Chemical group 0.000 claims description 2
- 239000000178 monomer Substances 0.000 claims description 2
- YHOSNAAUPKDRMI-UHFFFAOYSA-N n,n-di(propan-2-yl)prop-2-enamide Chemical compound CC(C)N(C(C)C)C(=O)C=C YHOSNAAUPKDRMI-UHFFFAOYSA-N 0.000 claims description 2
- OVHHHVAVHBHXAK-UHFFFAOYSA-N n,n-diethylprop-2-enamide Chemical compound CCN(CC)C(=O)C=C OVHHHVAVHBHXAK-UHFFFAOYSA-N 0.000 claims description 2
- 229940088644 n,n-dimethylacrylamide Drugs 0.000 claims description 2
- YLGYACDQVQQZSW-UHFFFAOYSA-N n,n-dimethylprop-2-enamide Chemical compound CN(C)C(=O)C=C YLGYACDQVQQZSW-UHFFFAOYSA-N 0.000 claims description 2
- BSCJIBOZTKGXQP-UHFFFAOYSA-N n-(2-hydroxyethyl)-2-methylprop-2-enamide Chemical compound CC(=C)C(=O)NCCO BSCJIBOZTKGXQP-UHFFFAOYSA-N 0.000 claims description 2
- RQAKESSLMFZVMC-UHFFFAOYSA-N n-ethenylacetamide Chemical compound CC(=O)NC=C RQAKESSLMFZVMC-UHFFFAOYSA-N 0.000 claims description 2
- SHIGCAOWAAOWIG-UHFFFAOYSA-N n-prop-2-enylformamide Chemical compound C=CCNC=O SHIGCAOWAAOWIG-UHFFFAOYSA-N 0.000 claims description 2
- 150000002892 organic cations Chemical class 0.000 claims description 2
- 125000004079 stearyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 claims description 2
- 239000001384 succinic acid Substances 0.000 claims description 2
- 150000005621 tetraalkylammonium salts Chemical class 0.000 claims description 2
- 239000000203 mixture Substances 0.000 abstract description 55
- 239000002253 acid Substances 0.000 abstract description 23
- 150000001768 cations Chemical class 0.000 abstract description 7
- 238000004061 bleaching Methods 0.000 abstract description 4
- 125000000391 vinyl group Chemical group [H]C([*])=C([H])[H] 0.000 abstract description 4
- 229920002554 vinyl polymer Polymers 0.000 abstract description 2
- 238000009472 formulation Methods 0.000 description 34
- 150000003839 salts Chemical class 0.000 description 22
- 239000000499 gel Substances 0.000 description 19
- MHAJPDPJQMAIIY-UHFFFAOYSA-N Hydrogen peroxide Chemical compound OO MHAJPDPJQMAIIY-UHFFFAOYSA-N 0.000 description 16
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 15
- KRKNYBCHXYNGOX-UHFFFAOYSA-N citric acid Chemical compound OC(=O)CC(O)(C(O)=O)CC(O)=O KRKNYBCHXYNGOX-UHFFFAOYSA-N 0.000 description 15
- 230000002378 acidificating effect Effects 0.000 description 14
- 125000000217 alkyl group Chemical group 0.000 description 14
- 150000007513 acids Chemical class 0.000 description 13
- 125000004432 carbon atom Chemical group C* 0.000 description 13
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 13
- DNIAPMSPPWPWGF-UHFFFAOYSA-N Propylene glycol Chemical compound CC(O)CO DNIAPMSPPWPWGF-UHFFFAOYSA-N 0.000 description 12
- 239000003795 chemical substances by application Substances 0.000 description 11
- 239000002562 thickening agent Substances 0.000 description 11
- 239000003599 detergent Substances 0.000 description 10
- OKKJLVBELUTLKV-UHFFFAOYSA-N Methanol Chemical compound OC OKKJLVBELUTLKV-UHFFFAOYSA-N 0.000 description 9
- 239000003960 organic solvent Substances 0.000 description 8
- 239000011734 sodium Substances 0.000 description 8
- QGZKDVFQNNGYKY-UHFFFAOYSA-O Ammonium Chemical compound [NH4+] QGZKDVFQNNGYKY-UHFFFAOYSA-O 0.000 description 7
- 239000002736 nonionic surfactant Substances 0.000 description 7
- 150000002978 peroxides Chemical class 0.000 description 7
- DGAQECJNVWCQMB-PUAWFVPOSA-M Ilexoside XXIX Chemical compound C[C@@H]1CC[C@@]2(CC[C@@]3(C(=CC[C@H]4[C@]3(CC[C@@H]5[C@@]4(CC[C@@H](C5(C)C)OS(=O)(=O)[O-])C)C)[C@@H]2[C@]1(C)O)C)C(=O)O[C@H]6[C@@H]([C@H]([C@@H]([C@H](O6)CO)O)O)O.[Na+] DGAQECJNVWCQMB-PUAWFVPOSA-M 0.000 description 6
- DKGAVHZHDRPRBM-UHFFFAOYSA-N Tert-Butanol Chemical compound CC(C)(C)O DKGAVHZHDRPRBM-UHFFFAOYSA-N 0.000 description 6
- ZMANZCXQSJIPKH-UHFFFAOYSA-N Triethylamine Chemical compound CCN(CC)CC ZMANZCXQSJIPKH-UHFFFAOYSA-N 0.000 description 6
- 150000001298 alcohols Chemical class 0.000 description 6
- 239000003945 anionic surfactant Substances 0.000 description 6
- 238000006116 polymerization reaction Methods 0.000 description 6
- 229910052708 sodium Inorganic materials 0.000 description 6
- 230000008719 thickening Effects 0.000 description 6
- 229910019142 PO4 Inorganic materials 0.000 description 5
- ZLMJMSJWJFRBEC-UHFFFAOYSA-N Potassium Chemical compound [K] ZLMJMSJWJFRBEC-UHFFFAOYSA-N 0.000 description 5
- 229920002125 Sokalan® Polymers 0.000 description 5
- QAOWNCQODCNURD-UHFFFAOYSA-L Sulfate Chemical compound [O-]S([O-])(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-L 0.000 description 5
- 235000014113 dietary fatty acids Nutrition 0.000 description 5
- 238000009826 distribution Methods 0.000 description 5
- 230000000694 effects Effects 0.000 description 5
- 150000002148 esters Chemical class 0.000 description 5
- 239000000194 fatty acid Substances 0.000 description 5
- 229930195729 fatty acid Natural products 0.000 description 5
- 239000003112 inhibitor Substances 0.000 description 5
- 229910052751 metal Inorganic materials 0.000 description 5
- 239000002184 metal Substances 0.000 description 5
- 235000021317 phosphate Nutrition 0.000 description 5
- 229920001223 polyethylene glycol Polymers 0.000 description 5
- 229910052700 potassium Inorganic materials 0.000 description 5
- 239000011591 potassium Substances 0.000 description 5
- 239000000047 product Substances 0.000 description 5
- 239000003760 tallow Substances 0.000 description 5
- QUSNBJAOOMFDIB-UHFFFAOYSA-N Ethylamine Chemical compound CCN QUSNBJAOOMFDIB-UHFFFAOYSA-N 0.000 description 4
- KFZMGEQAYNKOFK-UHFFFAOYSA-N Isopropanol Chemical compound CC(C)O KFZMGEQAYNKOFK-UHFFFAOYSA-N 0.000 description 4
- LRHPLDYGYMQRHN-UHFFFAOYSA-N N-Butanol Chemical compound CCCCO LRHPLDYGYMQRHN-UHFFFAOYSA-N 0.000 description 4
- 239000002202 Polyethylene glycol Substances 0.000 description 4
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 description 4
- FAPWRFPIFSIZLT-UHFFFAOYSA-M Sodium chloride Chemical compound [Na+].[Cl-] FAPWRFPIFSIZLT-UHFFFAOYSA-M 0.000 description 4
- DAKWPKUUDNSNPN-UHFFFAOYSA-N Trimethylolpropane triacrylate Chemical compound C=CC(=O)OCC(CC)(COC(=O)C=C)COC(=O)C=C DAKWPKUUDNSNPN-UHFFFAOYSA-N 0.000 description 4
- 239000000654 additive Substances 0.000 description 4
- 150000008051 alkyl sulfates Chemical class 0.000 description 4
- 125000000129 anionic group Chemical group 0.000 description 4
- 239000003792 electrolyte Substances 0.000 description 4
- 150000004665 fatty acids Chemical class 0.000 description 4
- 239000006260 foam Substances 0.000 description 4
- 239000011777 magnesium Substances 0.000 description 4
- 230000007935 neutral effect Effects 0.000 description 4
- 239000007800 oxidant agent Substances 0.000 description 4
- UEZVMMHDMIWARA-UHFFFAOYSA-M phosphonate Chemical compound [O-]P(=O)=O UEZVMMHDMIWARA-UHFFFAOYSA-M 0.000 description 4
- 229920000058 polyacrylate Polymers 0.000 description 4
- CDBYLPFSWZWCQE-UHFFFAOYSA-L sodium carbonate Substances [Na+].[Na+].[O-]C([O-])=O CDBYLPFSWZWCQE-UHFFFAOYSA-L 0.000 description 4
- 239000002904 solvent Substances 0.000 description 4
- 239000004094 surface-active agent Substances 0.000 description 4
- 125000003903 2-propenyl group Chemical group [H]C([*])([H])C([H])=C([H])[H] 0.000 description 3
- RSWGJHLUYNHPMX-UHFFFAOYSA-N Abietic-Saeure Natural products C12CCC(C(C)C)=CC2=CCC2C1(C)CCCC2(C)C(O)=O RSWGJHLUYNHPMX-UHFFFAOYSA-N 0.000 description 3
- CSCPPACGZOOCGX-UHFFFAOYSA-N Acetone Chemical compound CC(C)=O CSCPPACGZOOCGX-UHFFFAOYSA-N 0.000 description 3
- NIXOWILDQLNWCW-UHFFFAOYSA-M Acrylate Chemical compound [O-]C(=O)C=C NIXOWILDQLNWCW-UHFFFAOYSA-M 0.000 description 3
- 239000004971 Cross linker Substances 0.000 description 3
- IAZDPXIOMUYVGZ-UHFFFAOYSA-N Dimethylsulphoxide Chemical compound CS(C)=O IAZDPXIOMUYVGZ-UHFFFAOYSA-N 0.000 description 3
- 102000004190 Enzymes Human genes 0.000 description 3
- 108090000790 Enzymes Proteins 0.000 description 3
- PEDCQBHIVMGVHV-UHFFFAOYSA-N Glycerine Chemical compound OCC(O)CO PEDCQBHIVMGVHV-UHFFFAOYSA-N 0.000 description 3
- MUBZPKHOEPUJKR-UHFFFAOYSA-N Oxalic acid Chemical compound OC(=O)C(O)=O MUBZPKHOEPUJKR-UHFFFAOYSA-N 0.000 description 3
- KHPCPRHQVVSZAH-HUOMCSJISA-N Rosin Natural products O(C/C=C/c1ccccc1)[C@H]1[C@H](O)[C@@H](O)[C@@H](O)[C@@H](CO)O1 KHPCPRHQVVSZAH-HUOMCSJISA-N 0.000 description 3
- ULUAUXLGCMPNKK-UHFFFAOYSA-N Sulfobutanedioic acid Chemical class OC(=O)CC(C(O)=O)S(O)(=O)=O ULUAUXLGCMPNKK-UHFFFAOYSA-N 0.000 description 3
- 239000002585 base Substances 0.000 description 3
- 125000002511 behenyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 description 3
- WPYMKLBDIGXBTP-UHFFFAOYSA-N benzoic acid Chemical compound OC(=O)C1=CC=CC=C1 WPYMKLBDIGXBTP-UHFFFAOYSA-N 0.000 description 3
- 239000011575 calcium Substances 0.000 description 3
- 150000001735 carboxylic acids Chemical class 0.000 description 3
- 239000000919 ceramic Substances 0.000 description 3
- 239000007859 condensation product Substances 0.000 description 3
- 150000005690 diesters Chemical class 0.000 description 3
- 238000004851 dishwashing Methods 0.000 description 3
- 235000013399 edible fruits Nutrition 0.000 description 3
- 229940088598 enzyme Drugs 0.000 description 3
- 239000011521 glass Substances 0.000 description 3
- 239000001257 hydrogen Substances 0.000 description 3
- 229910052739 hydrogen Inorganic materials 0.000 description 3
- 125000002768 hydroxyalkyl group Chemical group 0.000 description 3
- 238000006386 neutralization reaction Methods 0.000 description 3
- 150000007524 organic acids Chemical class 0.000 description 3
- 239000003755 preservative agent Substances 0.000 description 3
- BDERNNFJNOPAEC-UHFFFAOYSA-N propan-1-ol Chemical class CCCO BDERNNFJNOPAEC-UHFFFAOYSA-N 0.000 description 3
- 229920005989 resin Polymers 0.000 description 3
- 239000011347 resin Substances 0.000 description 3
- 229920006395 saturated elastomer Polymers 0.000 description 3
- 239000000344 soap Substances 0.000 description 3
- 238000003860 storage Methods 0.000 description 3
- 239000000126 substance Substances 0.000 description 3
- 150000003467 sulfuric acid derivatives Chemical class 0.000 description 3
- KHPCPRHQVVSZAH-UHFFFAOYSA-N trans-cinnamyl beta-D-glucopyranoside Natural products OC1C(O)C(O)C(CO)OC1OCC=CC1=CC=CC=C1 KHPCPRHQVVSZAH-UHFFFAOYSA-N 0.000 description 3
- BJEPYKJPYRNKOW-REOHCLBHSA-N (S)-malic acid Chemical compound OC(=O)[C@@H](O)CC(O)=O BJEPYKJPYRNKOW-REOHCLBHSA-N 0.000 description 2
- ARXJGSRGQADJSQ-UHFFFAOYSA-N 1-methoxypropan-2-ol Chemical compound COCC(C)O ARXJGSRGQADJSQ-UHFFFAOYSA-N 0.000 description 2
- OZAIFHULBGXAKX-UHFFFAOYSA-N 2-(2-cyanopropan-2-yldiazenyl)-2-methylpropanenitrile Chemical compound N#CC(C)(C)N=NC(C)(C)C#N OZAIFHULBGXAKX-UHFFFAOYSA-N 0.000 description 2
- KUDUQBURMYMBIJ-UHFFFAOYSA-N 2-prop-2-enoyloxyethyl prop-2-enoate Chemical compound C=CC(=O)OCCOC(=O)C=C KUDUQBURMYMBIJ-UHFFFAOYSA-N 0.000 description 2
- CIWBSHSKHKDKBQ-JLAZNSOCSA-N Ascorbic acid Chemical compound OC[C@H](O)[C@H]1OC(=O)C(O)=C1O CIWBSHSKHKDKBQ-JLAZNSOCSA-N 0.000 description 2
- IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 description 2
- KRKNYBCHXYNGOX-UHFFFAOYSA-K Citrate Chemical compound [O-]C(=O)CC(O)(CC([O-])=O)C([O-])=O KRKNYBCHXYNGOX-UHFFFAOYSA-K 0.000 description 2
- RGHNJXZEOKUKBD-SQOUGZDYSA-N D-gluconic acid Chemical compound OC[C@@H](O)[C@@H](O)[C@H](O)[C@@H](O)C(O)=O RGHNJXZEOKUKBD-SQOUGZDYSA-N 0.000 description 2
- LYCAIKOWRPUZTN-UHFFFAOYSA-N Ethylene glycol Chemical compound OCCO LYCAIKOWRPUZTN-UHFFFAOYSA-N 0.000 description 2
- DBVJJBKOTRCVKF-UHFFFAOYSA-N Etidronic acid Chemical compound OP(=O)(O)C(O)(C)P(O)(O)=O DBVJJBKOTRCVKF-UHFFFAOYSA-N 0.000 description 2
- VZCYOOQTPOCHFL-OWOJBTEDSA-N Fumaric acid Chemical compound OC(=O)\C=C\C(O)=O VZCYOOQTPOCHFL-OWOJBTEDSA-N 0.000 description 2
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- 229910000359 iron(II) sulfate Inorganic materials 0.000 description 1
- SUMDYPCJJOFFON-UHFFFAOYSA-N isethionic acid Chemical class OCCS(O)(=O)=O SUMDYPCJJOFFON-UHFFFAOYSA-N 0.000 description 1
- BEJNERDRQOWKJM-UHFFFAOYSA-N kojic acid Chemical compound OCC1=CC(=O)C(O)=CO1 BEJNERDRQOWKJM-UHFFFAOYSA-N 0.000 description 1
- WZNJWVWKTVETCG-UHFFFAOYSA-N kojic acid Natural products OC(=O)C(N)CN1C=CC(=O)C(O)=C1 WZNJWVWKTVETCG-UHFFFAOYSA-N 0.000 description 1
- 229960004705 kojic acid Drugs 0.000 description 1
- 239000004310 lactic acid Substances 0.000 description 1
- 235000014655 lactic acid Nutrition 0.000 description 1
- 235000019421 lipase Nutrition 0.000 description 1
- 239000012669 liquid formulation Substances 0.000 description 1
- 239000012263 liquid product Substances 0.000 description 1
- 150000004668 long chain fatty acids Chemical class 0.000 description 1
- JDSHMPZPIAZGSV-UHFFFAOYSA-N melamine Chemical compound NC1=NC(N)=NC(N)=N1 JDSHMPZPIAZGSV-UHFFFAOYSA-N 0.000 description 1
- 150000002734 metacrylic acid derivatives Chemical class 0.000 description 1
- 125000005394 methallyl group Chemical group 0.000 description 1
- 238000000034 method Methods 0.000 description 1
- 229920000609 methyl cellulose Polymers 0.000 description 1
- 239000001923 methylcellulose Substances 0.000 description 1
- LVHBHZANLOWSRM-UHFFFAOYSA-N methylenebutanedioic acid Natural products OC(=O)CC(=C)C(O)=O LVHBHZANLOWSRM-UHFFFAOYSA-N 0.000 description 1
- 239000004200 microcrystalline wax Substances 0.000 description 1
- 235000019808 microcrystalline wax Nutrition 0.000 description 1
- 150000007522 mineralic acids Chemical class 0.000 description 1
- ZIUHHBKFKCYYJD-UHFFFAOYSA-N n,n'-methylenebisacrylamide Chemical compound C=CC(=O)NCNC(=O)C=C ZIUHHBKFKCYYJD-UHFFFAOYSA-N 0.000 description 1
- 150000002823 nitrates Chemical class 0.000 description 1
- 125000004433 nitrogen atom Chemical group N* 0.000 description 1
- 235000020824 obesity Nutrition 0.000 description 1
- OXOUKWPKTBSXJH-UHFFFAOYSA-J octadecanoate;titanium(4+) Chemical class [Ti+4].CCCCCCCCCCCCCCCCCC([O-])=O.CCCCCCCCCCCCCCCCCC([O-])=O.CCCCCCCCCCCCCCCCCC([O-])=O.CCCCCCCCCCCCCCCCCC([O-])=O OXOUKWPKTBSXJH-UHFFFAOYSA-J 0.000 description 1
- 239000003921 oil Substances 0.000 description 1
- 235000019198 oils Nutrition 0.000 description 1
- JRZJOMJEPLMPRA-UHFFFAOYSA-N olefin Natural products CCCCCCCC=C JRZJOMJEPLMPRA-UHFFFAOYSA-N 0.000 description 1
- 150000001451 organic peroxides Chemical class 0.000 description 1
- 239000003791 organic solvent mixture Substances 0.000 description 1
- 235000006408 oxalic acid Nutrition 0.000 description 1
- 229910052760 oxygen Inorganic materials 0.000 description 1
- 239000001301 oxygen Substances 0.000 description 1
- 239000005022 packaging material Substances 0.000 description 1
- 238000004806 packaging method and process Methods 0.000 description 1
- 239000002540 palm oil Substances 0.000 description 1
- UWJJYHHHVWZFEP-UHFFFAOYSA-N pentane-1,1-diol Chemical compound CCCCC(O)O UWJJYHHHVWZFEP-UHFFFAOYSA-N 0.000 description 1
- 125000000864 peroxy group Chemical group O(O*)* 0.000 description 1
- 229960005323 phenoxyethanol Drugs 0.000 description 1
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 description 1
- NBIIXXVUZAFLBC-UHFFFAOYSA-K phosphate Chemical compound [O-]P([O-])([O-])=O NBIIXXVUZAFLBC-UHFFFAOYSA-K 0.000 description 1
- 239000010452 phosphate Substances 0.000 description 1
- 229910052615 phyllosilicate Inorganic materials 0.000 description 1
- 229920003023 plastic Polymers 0.000 description 1
- 239000004033 plastic Substances 0.000 description 1
- 229920000172 poly(styrenesulfonic acid) Polymers 0.000 description 1
- 229920002401 polyacrylamide Polymers 0.000 description 1
- 229920001748 polybutylene Polymers 0.000 description 1
- 235000013856 polydextrose Nutrition 0.000 description 1
- 239000001259 polydextrose Substances 0.000 description 1
- 229940035035 polydextrose Drugs 0.000 description 1
- 229920000573 polyethylene Polymers 0.000 description 1
- 239000003505 polymerization initiator Substances 0.000 description 1
- 229920005862 polyol Polymers 0.000 description 1
- 150000003077 polyols Chemical class 0.000 description 1
- 229920000137 polyphosphoric acid Polymers 0.000 description 1
- 229920001155 polypropylene Polymers 0.000 description 1
- 150000007519 polyprotic acids Polymers 0.000 description 1
- 229940005642 polystyrene sulfonic acid Drugs 0.000 description 1
- 229920002451 polyvinyl alcohol Polymers 0.000 description 1
- 159000000001 potassium salts Chemical class 0.000 description 1
- 235000019353 potassium silicate Nutrition 0.000 description 1
- 239000002244 precipitate Substances 0.000 description 1
- 230000002335 preservative effect Effects 0.000 description 1
- 238000002203 pretreatment Methods 0.000 description 1
- 150000003138 primary alcohols Chemical class 0.000 description 1
- 125000002572 propoxy group Chemical group [*]OC([H])([H])C(C([H])([H])[H])([H])[H] 0.000 description 1
- 230000001681 protective effect Effects 0.000 description 1
- ROSDSFDQCJNGOL-UHFFFAOYSA-N protonated dimethyl amine Natural products CNC ROSDSFDQCJNGOL-UHFFFAOYSA-N 0.000 description 1
- 238000000197 pyrolysis Methods 0.000 description 1
- 125000001453 quaternary ammonium group Chemical group 0.000 description 1
- 238000010526 radical polymerization reaction Methods 0.000 description 1
- 150000003254 radicals Chemical class 0.000 description 1
- 239000012429 reaction media Substances 0.000 description 1
- 238000000518 rheometry Methods 0.000 description 1
- 230000000630 rising effect Effects 0.000 description 1
- 150000003333 secondary alcohols Chemical class 0.000 description 1
- 239000003352 sequestering agent Substances 0.000 description 1
- 150000004760 silicates Chemical class 0.000 description 1
- 229920002545 silicone oil Polymers 0.000 description 1
- 229910000029 sodium carbonate Inorganic materials 0.000 description 1
- 229940079827 sodium hydrogen sulfite Drugs 0.000 description 1
- 235000010267 sodium hydrogen sulphite Nutrition 0.000 description 1
- 159000000000 sodium salts Chemical class 0.000 description 1
- 229910052911 sodium silicate Inorganic materials 0.000 description 1
- 229910052938 sodium sulfate Inorganic materials 0.000 description 1
- 235000011152 sodium sulphate Nutrition 0.000 description 1
- MWNQXXOSWHCCOZ-UHFFFAOYSA-L sodium;oxido carbonate Chemical compound [Na+].[O-]OC([O-])=O MWNQXXOSWHCCOZ-UHFFFAOYSA-L 0.000 description 1
- 235000010199 sorbic acid Nutrition 0.000 description 1
- 239000004334 sorbic acid Substances 0.000 description 1
- 229940075582 sorbic acid Drugs 0.000 description 1
- 239000008107 starch Substances 0.000 description 1
- 235000019698 starch Nutrition 0.000 description 1
- 239000007858 starting material Substances 0.000 description 1
- 238000004659 sterilization and disinfection Methods 0.000 description 1
- PJANXHGTPQOBST-UHFFFAOYSA-N stilbene Chemical class C=1C=CC=CC=1C=CC1=CC=CC=C1 PJANXHGTPQOBST-UHFFFAOYSA-N 0.000 description 1
- 239000000758 substrate Substances 0.000 description 1
- 150000005846 sugar alcohols Polymers 0.000 description 1
- DIORMHZUUKOISG-UHFFFAOYSA-N sulfoformic acid Chemical compound OC(=O)S(O)(=O)=O DIORMHZUUKOISG-UHFFFAOYSA-N 0.000 description 1
- 238000006277 sulfonation reaction Methods 0.000 description 1
- 150000003460 sulfonic acids Chemical class 0.000 description 1
- 239000000725 suspension Substances 0.000 description 1
- 229920001059 synthetic polymer Polymers 0.000 description 1
- 229940104261 taurate Drugs 0.000 description 1
- XOAAWQZATWQOTB-UHFFFAOYSA-N taurine Chemical compound NCCS(O)(=O)=O XOAAWQZATWQOTB-UHFFFAOYSA-N 0.000 description 1
- LDHQCZJRKDOVOX-UHFFFAOYSA-N trans-crotonic acid Natural products CC=CC(O)=O LDHQCZJRKDOVOX-UHFFFAOYSA-N 0.000 description 1
- URAYPUMNDPQOKB-UHFFFAOYSA-N triacetin Chemical compound CC(=O)OCC(OC(C)=O)COC(C)=O URAYPUMNDPQOKB-UHFFFAOYSA-N 0.000 description 1
- VPYJNCGUESNPMV-UHFFFAOYSA-N triallylamine Chemical compound C=CCN(CC=C)CC=C VPYJNCGUESNPMV-UHFFFAOYSA-N 0.000 description 1
- GETQZCLCWQTVFV-UHFFFAOYSA-N trimethylamine Chemical compound CN(C)C GETQZCLCWQTVFV-UHFFFAOYSA-N 0.000 description 1
- GETQZCLCWQTVFV-UHFFFAOYSA-O trimethylammonium Chemical compound C[NH+](C)C GETQZCLCWQTVFV-UHFFFAOYSA-O 0.000 description 1
- 150000003673 urethanes Chemical class 0.000 description 1
- 239000003981 vehicle Substances 0.000 description 1
- ZTWTYVWXUKTLCP-UHFFFAOYSA-N vinylphosphonic acid Chemical class OP(O)(=O)C=C ZTWTYVWXUKTLCP-UHFFFAOYSA-N 0.000 description 1
- 239000001993 wax Substances 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C11—ANIMAL OR VEGETABLE OILS, FATS, FATTY SUBSTANCES OR WAXES; FATTY ACIDS THEREFROM; DETERGENTS; CANDLES
- C11D—DETERGENT COMPOSITIONS; USE OF SINGLE SUBSTANCES AS DETERGENTS; SOAP OR SOAP-MAKING; RESIN SOAPS; RECOVERY OF GLYCEROL
- C11D3/00—Other compounding ingredients of detergent compositions covered in group C11D1/00
- C11D3/16—Organic compounds
- C11D3/37—Polymers
- C11D3/3746—Macromolecular compounds obtained by reactions only involving carbon-to-carbon unsaturated bonds
- C11D3/378—(Co)polymerised monomers containing sulfur, e.g. sulfonate
Definitions
- the present invention relates to liquid washing, cleaning, disinfecting and Bleaching agents containing hydrophobically modified copolymers based on Acryloyidimethyltaurine.
- the finished formulations are characterized by a favorable rheological behavior, as well as good compatibility with others Components off. They have a high storage stability, especially high Stability of hydrolysis-sensitive components, for example oxidizing agents in the formulations, preferably in acidic formulations and are UV stable.
- formulations for Washing, cleaning and disinfecting to viscosities greater than 100 cP.
- formulations with acidic Character (pH ⁇ 5) Due to the acidic environment, it also manages to be pH-sensitive To stabilize oxidizing agents such as hydrogen peroxide permanently and thus accessible to new applications in the cleaning and hygiene sector close. Fortunately, these formulations are additionally characterized high UV stability. This allows the use of transparent Packaging materials that are currently in great demand in the market.
- Comonomers with more than one polymerizable unit lead to crosslinking the structures according to the invention.
- the copolymers according to the invention preferably have a molecular weight M w of from 10 3 g / mol to 10 9 g / mol, more preferably from 10 4 to 10 7 g / mol, particularly preferably from 5 ⁇ 10 4 to 5 ⁇ 10 6 g / mol.
- M w for the purposes of this invention is generally to be determined by GPC versus polystyrene sulfonic acid.
- the acryloyldimethyltaurates may be the inorganic or organic salts of acryloyldimethyltaurine acid. Preference is given to the Li + , Na + , K + , Mg ++ , Ca ++ , Al +++ and / or NH 4 + salts.
- the monoalkylammonium, dialkylammonium, trialkylammonium and / or tetraalkylammonium salts where the alkyl substituents of the amines can independently of one another be (C 1 -C 22 ) -alkyl radicals which are optionally substituted by up to 3 (C 2 -) C 10 ) hydroxyalkyl groups may be occupied.
- the alkyl substituents of the amines can independently of one another be (C 1 -C 22 ) -alkyl radicals which are optionally substituted by up to 3 (C 2 -) C 10 ) hydroxyalkyl groups may be occupied.
- ethoxylated ammonium compounds with different degrees of ethoxylation are preferred. It should be noted that mixtures of two or more of the above compounds are also within the scope of the invention.
- the degree of neutralization of acryloyldimethyltaurine can be between 0 and 100% be particularly preferred is a degree of neutralization of above 80%.
- the content of Acryloyldimethyltaurine or acryloyldimethyltaurate 0.1 to 99.9% by weight, preferably 20 to 99.5 wt .-%, particularly preferably 50 to 98 wt .-% amount.
- Macromonomer structural unit b
- copolymerization can also mixtures of chemically different macromonomers b) used become.
- the content of Macromonomers preferably 0.1 to 99.9 wt .-%, in particular 0.5 to 80 wt .-%, particularly preferably 2 to 50 wt .-% amount.
- Preferred as macromonomers b) are compounds according to formula (I).
- R 1 represents a polymerizable function from the group of vinylically unsaturated compounds, which are suitable for the construction of polymeric structures by free radicals.
- R 1 represents a vinyl, allyl, methallyl, methylvinyl, acrylic, methacrylic, crotonyl, senecionyl, itaconyl, maleinyl, fumarylo or styryl radical.
- a suitable bridging group Y is required.
- Preferred bridges Y are -O-, -C (O) -, - C (O) -O-, -S-, -O-CH 2 -CH (O -) - CH 2 OH, -O-CH 2 - CH (OH) -CH 2 O-, -O-SO 2 -O-, -O-SO-O-, -PH-, -P (CH 3 ) -, -PO 3 -, -NH- and -N (CH 3 ) -, more preferably -O-.
- the polymeric middle part of the macromonomer is represented by the discrete repeating units A, B, C and D.
- Preferred repeating units A, B, C and D are derived from acrylamide, methacrylamide, ethylene oxide, propylene oxide, AMPS, acrylic acid, methacrylic acid, methyl methacrylate, acrylonitrile, maleic acid, vinyl acetate, styrene, 1,3-butadiene, isoprene, isobutene, diethylacrylamide and diisopropylacrylamide , in particular of ethylene oxide and propylene oxide.
- indices v, w, x and z in formula (I) represent the stoichiometric coefficients relating to repeating units A, B, C and D.
- v, w, x and z are independently 0 to 500, preferably 1 to 30, wherein Sum of the four coefficients on average must be ⁇ 1.
- the distribution of repeating units via the macromonomer chain can be random, block-like, alternating or gradient-like.
- R 2 represents a linear or branched aliphatic, olefinic, cycloaliphatic, arylaliphatic or aromatic (C 1 -C 50 ) -hydrocarbon radical, OH, -NH 2 , -N (CH 3 ) 2 or is identical to the structural unit [-YR 1 ].
- R 2 equal to [-YR 1 ] are difunctional macromonomers, which are suitable for crosslinking of the copolymers.
- macromonomers b) are acrylic or methacrylic monofunctionalized alkyl ethoxylates according to formula (II).
- R 3 , R 4 , R 5 and R 6 independently of one another are hydrogen or n-aliphatic, iso-aliphatic, olefinic, cycloaliphatic, arylaliphatic or aromatic (C 1 -C 30 ) -hydrocarbon radicals.
- R 3 and R 4 are preferably H or -CH 3 , particularly preferably H.
- R 5 is H or -CH 3
- R 6 is equal to an n-aliphatic, iso-aliphatic, olefinic, cycloaliphatic, arylaliphatic or aromatic ( C 1 -C 30 ) hydrocarbon radical.
- m and n are again the stoichiometric coefficients concerning the Ethylene oxide units (EO) and propylene oxide units (PO).
- EO Ethylene oxide units
- PO propylene oxide units
- m and n amount independently 0 to 500, preferably 1 to 30, wherein the sum of m and n must be on average ⁇ 1.
- the distribution of EO and PO units over the Macromonomer chain can be random, blocky, alternating or gradient-like be.
- Y stands for the bridges mentioned above.
- Particularly preferred macromonomers have the following structure according to formula (II): description R 3 R 4 R 5 R 6 m n ®LA-030 methacrylate H H -CH 3 lauryl 3 0 LA-070 methacrylate H H -CH 3 lauryl 7 0 LA-200 methacrylate H H -CH 3 lauryl 20 0 LA-250 methacrylate H H -CH 3 lauryl 25 0 T-080 methacrylate H H -CH 3 -Tallow 8th 0 T-080 acrylate H H H -Tallow 8th 0 T-250 methacrylate H H -CH 3 -Tallow 25 0 T-250-crotonate -CH 3 H -CH 3 -Tallow 25 0 OC-030 methacrylate H H -CH 3 octyl 3 0 OC-105 methacrylate H H -CH 3 octyl 10 5 Behenyl 010-metharyl H H H
- the molecular weight of the macromonomers b) is preferably 200 g / mol to 10 6 g / mol, more preferably 150 to 10 4 g / mol and particularly preferably 200 to 5000 g / mol.
- comonomers c) all olefinically unsaturated monomers can be used whose reaction parameters are copolymerized with Acryloyldimethyltaurinklare and / or Acryloyldimethyltauraten in the respective Allow reaction media.
- N-vinylamides preferably N-vinylformamide (VIFA), N-vinylmethylformamide, N-vinylmethylacetamide (VIMA) and N-vinylacetamide; cyclic N-vinylamides (N-vinyllactams) having a ring size of 3 to 9, preferably N-vinylpyrrolidone (NVP) and N-vinylcaprolactam; Amides of acrylic and Methacrylic acid, preferably acrylamide, methacrylamide, N, N-dimethylacrylamide, N, N-diethylacrylamide and N, N-diisopropylacrylamide; alkoxylated acrylic and Methacrylamides, preferably hydroxyethyl methacrylate, hydroxymethylmethacrylamide, Hydroxyethyl methacrylamide, hydroxypropyl methacrylamide and succinic acid mono [2- (methacryloyloxy) ethyl ester];
- VIFA N-vinyl
- one or more unsaturated carboxylic acids or their salts be polymerized into the structure.
- Particularly preferred are acrylic acid, Methacrylic acid, styrenesulfonic acid, maleic acid, fumaric acid, crotonic acid, Itaconic acid and senecioic acid.
- Preferred as counterions of the acids are Li + , Na + , K + , Mg ++ , Ca ++ , Al +++ , NH 4 + , monoalkylammonium, dialkylammonium, trialkylammonium and / or tetraalkylammonium radicals, it being the case with the Alkyl substituents of the amines independently of one another can be (C 1 -C 22 ) -alkyl radicals, which may optionally be occupied by up to 3 (C 2 -C 10 ) -hydroxyalkyl groups.
- the degree of neutralization of the carboxylic acids can be between 0 and 100%.
- the copolymers according to the invention are crosslinked, i. they contain comonomers (structural unit c) with at least two polymerizable vinyl groups.
- Preferred crosslinkers are methylenebisacrylamide; methylenebismethacrylamide; Esters of unsaturated mono- and polycarboxylic acids with polyols, preferably diacrylates and triacrylates or methacrylates, more preferably butanediol and ethylene glycol diacrylate or methacrylate, trimethylolpropane triacrylate (TMPTA) and allyl compounds, preferably allyl (meth) acrylate, triallyl cyanurate, maleic acid diallyl ester, polyallyl ester, tetraallyloxyethane , Triallylamine, tetraallylethylenediamine; Allyl ester of phosphoric acid; and / or vinylphosphonic acid derivatives.
- Particularly preferred crosslinkers are trimethylolpropane triacrylate (TMPTA) and timethylolpropane trimethacrylate (TMPTMA).
- the proportion by weight of comonomers (structural unit c), based on the Total mass of the copolymers of the invention is preferably from 0.01 to 90 wt .-%, particularly preferably 0.05 to 50 wt .-% and particularly preferably 0.1 to 40 wt .-%.
- a polymerization medium all organic or inorganic Solvents that are concerned with radical polymerization reactions largely inert behavior and advantageously the formation of medium or high Allow molecular weights.
- lower Alcohols preferably methanol, ethanol, propanols, iso-, sec- and t-butanol, especially preferred is t-butanol, hydrocarbons having 1 to 30 Carbon atoms and mixtures of the aforementioned compounds.
- the polymerization reaction preferably takes place in the temperature range between 0 and 150 ° C, more preferably between 10 and 100 ° C, both at atmospheric pressure as even under increased or reduced pressure. If necessary, the Polymerization also under a protective gas atmosphere, preferably below Nitrogen, to be carried out.
- a protective gas atmosphere preferably below Nitrogen
- high-energy electromagnetic radiation mechanical energy or the usual chemical polymerization initiators, such as organic peroxides, for example benzoyl peroxide, tert-butyl hydroperoxide, methyl ethyl ketone peroxide, cumene hydroperoxide, dilauroyl peroxide (DLP) or azo initiators, such as azodiisobutyronitrile (AIBN) can be used.
- organic peroxides for example benzoyl peroxide, tert-butyl hydroperoxide, methyl ethyl ketone peroxide, cumene hydroperoxide, dilauroyl peroxide (DLP) or azo initiators, such as azodiisobutyronitrile (AIBN)
- AIBN azodiisobutyronitrile
- inorganic peroxy compounds such as (NH 4 ) 2 S 2 O 8 , K 2 S 2 O 8 or H 2 O 2 , optionally in combination with reducing agents (eg sodium hydrogen sulfite, ascorbic acid, iron (II) sulfate, etc.) or redox systems containing as reducing component an aliphatic or aromatic sulfonic acid (eg benzenesulfonic acid, toluenesulfonic acid etc.).
- reducing agents eg sodium hydrogen sulfite, ascorbic acid, iron (II) sulfate, etc.
- redox systems containing as reducing component an aliphatic or aromatic sulfonic acid (eg benzenesulfonic acid, toluenesulfonic acid etc.).
- the polymerization reaction may e.g. as precipitation polymerization, Emulsion polymerization, bulk polymerization, solution polymerization or Gel polymerization led.
- Particularly advantageous for the property profile of Copolymers of the invention is the precipitation polymerization, preferably in tert-butanol.
- the above-described hydrophobically modified Copolymers based on acryloyldimethyltaurate generally in all wash, Cleaning, disinfecting and bleaching agents of any kind are used. They are preferably used as thickeners in acidic Detergent formulations for hard surfaces of ceramic, metal, glass or plastic, for example in liquid all-purpose cleaners, in the sanitary sector, For example, liquid toilet block, limesolvent bath cleaners, but also Dishwashing detergents. Furthermore, they are suitable for use in Stain removers, liquid detergents and laundry bleaches.
- the washing, cleaning, disinfecting and bleaching agents according to the invention may be in the form of aqueous, aqueous / organic, in particular aqueous / alcoholic and organic formulations are present. Further Embodiments may be: emulsions, dispersions, gels and Suspensions.
- the washing, cleaning, disinfecting and bleaching agents according to the invention contain an acidic component.
- Suitable organic or inorganic acids preferably organic acids, more preferably alpha-hydroxy acids and acids selected from glycolic, lactic, citric, tartaric, mandelic, salicylic, ascorbic, pyruvic, oligooxa mono- and dicarboxylic, fumaric, retinoic, aliphatic and organic Sulfonic acids, benzoic acid, kojic acid, fruit acid, malic acid, gluconic acid, galacturonic acid, acidic plant and / or fruit extracts and their derivatives.
- preferred embodiments may include oxidizing agents, in particular Hydrogen peroxide or its addition compounds, for example the Addition compounds of hydrogen peroxide to urea, melamine or Sodium borate or solutions of perborate or percarbonate optionally also contain caroate.
- oxidizing agents in particular Hydrogen peroxide or its addition compounds, for example the Addition compounds of hydrogen peroxide to urea, melamine or Sodium borate or solutions of perborate or percarbonate optionally also contain caroate.
- the preparations according to the invention may contain oxidizing agents in amounts of 0.1 to 30 wt .-%, particularly preferably 0.5 to 18 wt .-%, in particular 1.5 to 9 wt .-% included.
- washing, cleaning, disinfecting and bleaching agents according to the invention may be surfactants of nonionic, anionic, cationic or amphoteric nature and customary auxiliaries and additives in different amounts.
- Preferred nonionic surfactants are fatty alcohol ethoxylates containing from about 1 to about 25 moles of ethylene oxide.
- the alkyl chain of the aliphatic alcohols may be linear or branched, primary or secondary, and generally contains from 8 to 22 carbon atoms. Particularly preferred are the condensation products of alcohols containing an alkyl chain of 10 to 20 carbons with 2 to 18 moles of ethylene oxide per mole of alcohol.
- the alkyl chain can be saturated or unsaturated.
- the alcohol ethoxylates may have a narrow homolog distribution of the ethylene oxide ("narrow range ethoxylates") or a broad homolog distribution of the ethylene oxide ("broad range ethoxylates").
- nonionic surfactants of this type are Tergitol TM 15-S-9 (condensation product of a C 11 -C 15 linear secondary alcohol with 9 moles of ethylene oxide), Tergitol TM 24-L NMW (condensation product of a C 12 -C 14 linear primary Alcohol with 6 moles of ethylene oxide with narrow molecular weight distribution). Also included in this product class are the Genapol TM brands from Clariant GmbH.
- nonionic surfactants such as polyethylene, polypropylene and Polybutylene oxide adducts of alkylphenols having 6 to 12 C atoms in the alkyl chain, Addition products of ethylene oxide with a hydrophobic base formed from the Condensation of propylene oxide with propylene glycol or addition products of Ethylene oxide with a reaction product of propylene oxide and ethylenediamine.
- semipolar nonionic surfactants for example amine oxides of the formula III where R 8 is an alkyl, hydroxyalkyl or alkylphenol group or mixtures thereof having a chain length of 8 to 22 carbon atoms; R 9 is an alkylene or hydroxyalkylene group having 2 to 3 carbon atoms or mixtures thereof; R 10 is an alkyl or hydroxyalkyl group having 1 to 3 carbon atoms or a polyethylene oxide group having 1 to 3 ethylene oxide units.
- the R 10 / R 9 groups may be linked together via an oxygen or nitrogen atom and thus form a ring.
- These amine oxides particularly include C 10 -C 18 alkyl dimethyl amine oxides and C 8 -C 12 alkoxyethyl dihydroxyethyl amine oxides.
- the mixtures according to the invention also contain anionic surfactants.
- Suitable anionic surfactants are, in particular, straight-chain and branched Alkyl sulfates, sulfonates, carboxylates, phosphates, alkyl ester sulfonates, Arylalkylsulfonate, alkyl ether sulfates and mixtures of the above Links. The following are some of the candidate types of anionic surfactants are described in more detail.
- Alkyl ester sulfonates are linear esters of C 8 -C 20 carboxylic acids (ie, fatty acids) that are sulfonated by SO 3 , as described in The Journal of the American Oil Chemists Society, 52 (1975), pp. 323-329.
- Suitable starting materials are natural fatty derivatives, such as tallow or palm oil fatty acid.
- Alkyl sulfates are water-soluble salts or acids of the formula ROSO 3 M, wherein R is preferably a C 10 -C 24 -hydrocarbon radical, preferably an alkyl or hydroxyalkyl radical having 10 to 20 C-atoms, particularly preferably a C 12 -C 18 -alkyl or hydroxyalkyl radical , M is hydrogen or a cation, for example an alkali metal cation (eg sodium, potassium, lithium) or ammonium or substituted ammonium, for example a methyl, dimethyl and trimethylammonium cation or a quaternary ammonium cation, such as tetramethylammonium and dimethylpiperidinium cation and quaternary ammonium cations, derived from alkylamines such as ethylamine, diethylamine, triethylamine and mixtures thereof. Alkyl chains with C 12 -C 16 are preferred for low washing temperatures (eg below about 50
- the alkyl ether sulfates are water-soluble salts or acids of the formula RO (A) m SO 3 M, where R is an unsubstituted C 10 -C 24 -alkyl or hydroxyalkyl radical having 10 to 24 C atoms, preferably a C 12 -C 20 -alkyl radical. or hydroxyalkyl radical, particularly preferably a C 12 -C 18 -alkyl or hydroxyalkyl radical.
- A is an ethoxy or propoxy moiety
- m is a number greater than 0, typically between about 0.5 and about 6, more preferably between about 0.5 and about 3
- M is a hydrogen atom or a cation such as for example, a metal cation (eg, sodium, potassium, lithium, calcium, magnesium, etc.), ammonium, or a substituted ammonium cation.
- substituted ammonium cations are methyl, dimethyl, trimethylammonium and quaternary ammonium cations such as tetramethylammonium and dimethylpiperidinium cations, as well as those derived from alkylamines such as ethylamine, diethylamine, triethylamine, mixtures thereof and the like.
- C 12 -C 18 -alkyl polyethoxylate (1.0) sulfate, C 12 -C 18 -alkyl polyethoxylate (2,25) sulfate, C 12 -C 18 -alkyl polyethoxylate (3.0 ) sulfate, C 12 -C 18 alkyl polyethoxylate (4.0) sulfate, wherein the cation is sodium or potassium.
- anionic surfactants useful in laundry detergents and cleaners are C 8 -C 24 olefin sulfonates, sulfonated polycarboxylic acids prepared by sulfonation of pyrolysis products of alkaline earth metal citrates such as described in British Patent GB 1,082,179, alkyl glycerol sulfates, fatty acyl glycerol sulfates, oleyl glycerol sulfates, Alkylphenol ether sulfates, primary paraffin sulfonates, alkyl phosphates, alkyl ether phosphates, isethionates such as acyl isethionates, N-acyl taurides, alkyl succinamates, sulfosuccinates, monoesters of sulfosuccinates (especially saturated and unsaturated C 12 -C 18 monoesters) and diesters of sulfosuccinates (especially
- Resin acids or hydrogenated resin acids such as rosin or hydrogenated rosin or tall oil resins and tall oil rosin acids are also useful. Further examples are described in "Surface Active Agents and Detergents" (Vol. I and II, Schwartz, Perry and Berch). A variety of such surfactants are also claimed in U.S. Patent 3,929,678.
- amphoteric surfactants used in the formulations of the present invention Invention can be used, especially those that are widely used as derivatives of aliphatic secondary and tertiary amines are described in which the Aliphatic radical may be linear or branched and in which one of the aliphatic substituents between. Contains 8 to 18 carbon atoms and one anionic, water-soluble group, such as e.g. Carboxy, sulfonate, sulfate, phosphate or phosphonate.
- amphoteric surfactants are alkyl dimethyl betaines, Alkylamidobetaines and Alkyldipolyethoxybetaine having an alkyl radical which is linear or be branched, with. 8 to 22 carbon atoms, preferably 8 to 18 Carbon atoms and particularly preferably with. 12 to. 18 carbon atoms. These compounds are e.g. from the Clariant GmbH under the trade name Genagen® CAB markets.
- the washing and cleaning agents contain, depending on the application, in addition to the mentioned surfactants nor the respectively specific auxiliaries and additives
- auxiliaries and additives For example, builders, salts (electrolytes), bleaches, bleach activators, optical Brighteners, complexing agents, grayness inhibitors, solubilizers, enzymes, Thickeners, preservatives, perfumes and dyes, pearlescing agents, Foam inhibitors, sequestering agents.
- organic and inorganic builders are neutral or especially alkaline salts that precipitate calcium ions or to bind complex.
- Suitable and especially ecological harmless builders such as fine crystalline, synthetic hydrous Zeolites of type NaA, which have a calcium binding capacity in the range of 100 to 200 mg CaO / g find a preferred use.
- non-aqueous Systems phyllosilicates are preferably used. Zeolite and the Layered silicates may be present in an amount of up to 20% by weight on average.
- Useful organic builders are, for example, those which are preferably in the form their sodium salts used percarboxylic acids, such as citric acid and Nitriloacetate (NTA), ethylenediaminetetraacetic acid, if such use of ecological reasons is not objectionable. Analogous to this can also polymeric carboxylates and their salts are used. These include for example, the salts of homopolymeric or copolymeric polyacrylates, Polymethyacrylate and in particular copolymers of acrylic acid with maleic acid, preferably those of 50% to 10% maleic acid and also polyvinylpyrrolidone and urethanes.
- the molecular weight of the homopolymers is generally between 1000 and 100,000, that of the copolymers between 2000 and 200,000, preferably 50,000 to 120,000, based on the free acid, in particular also suitable water-soluble polyacrylates, for example, with about 1% of a Polyallylethers of sucrose are cross-linked and have a molecular weight own over one million. Examples are those under the name Carbopol 940 and 941 available polymers.
- the crosslinked polyacrylates are used in Amounts not exceeding 1% by weight, preferably in amounts of from 0.2 to 0.7 wt .-% used.
- the agents according to the invention contain salts.
- the salts are heteropolar compounds whose crystal lattice has at least one cation species other than hydrogen ions and at least one anion species other than hydroxide ions.
- the agents according to the invention preferably contain inorganic salts, more preferably ammonium or metal salts, preferably halides, oxides, carbonates, bicarbonates, phosphates, sulfates, nitrates, most preferably sodium chloride; and / or organic salts, preferably ammonium or metal salts, preferably glycolic, lactic, citric, tartaric, mandelic, salicylic, ascorbic, pyruvic, fumaric, retinoic, sulfonic, benzoic, kojic, fruit, malic, gluconic, galacturonic.
- the salts are preferably derived from mono- or polybasic acids and bases, preferably from monovalent acids and / or monovalent bases. Particularly preferred are sodium, potassium and ammonium salts.
- the agents may also contain mixtures of different salts.
- the agents usually contain the electrolytes in a concentration of from 0.01 to 50% by weight, preferably from 0.1 to 50% by weight, particularly preferably from 0.5 to 10% by weight.
- the agents according to the invention can be used as foam inhibitors Fatty acid alkyl ester alkoxylates, organopolysiloxanes and mixtures thereof with microfine, optionally silanized silica and paraffins, waxes, Microcrystalline waxes and their mixtures with silanized silica. With Advantage may also be used mixtures of different foam inhibitors, e.g. those made of silicone oil, paraffin oil or waxes. Preferably Foam inhibitors to a granular, water-soluble or dispersible Vehicle bound.
- the liquid detergents can optical brighteners, for example derivatives of Diaminostilbendisulfonklare or their alkali metal salts, which are well in have the dispersion incorporated.
- the maximum content of brighteners in the inventive compositions is 0.5 wt .-%, preferably amounts of 0.02 to 0.25 wt .-% used.
- the desired viscosity of the agents can be achieved by adding water and / or organic solvents or by adding a combination of organic Solvents and other thickening agents can be adjusted.
- Alcohols having 1 to 4 carbon atoms such as methanol, ethanol, propanol, isopropanol, straight-chain and branched butanol, glycerol and mixtures of the alcohols mentioned are preferably used.
- More preferred alcohols are polyethylene glycols having a molecular weight less than 2,000. In particular, use of polyethylene glycol having a molecular weight of between 200 and 600 and up to 45% by weight and polyethylene glycol having a molecular weight of between 400 and 600 in amounts of 5 to 25 wt .-% preferred.
- An advantageous mixture of solvents consists of monomeric alcohol, for example ethanol and polyethylene glycol in a ratio of 0.5: 1 to 1.2: 1, wherein the liquid detergent according to the invention may contain 8 to 12 wt .-% of such a mixture.
- suitable solvents include triacetin (glycerol triacetate) and 1-methoxy-2-propanol.
- Preferred thickeners are hardened castor oil, salts of long-chain fatty acids, preferably in amounts of from 0 to 5% by weight and in particular in amounts of from 0.5 to 2% by weight, for example sodium.
- Potassium, aluminum, magnesium and titanium stearates or the sodium and / or potassium salts of behenic acid as well as polysaccharides, in particular xanthan gum, guar guar, agar agar, alginates and tyloses, carboxymethyl cellulose and hydroxyethyl cellulose, and also higher molecular weight polyethylene glycol mono- and diesters of fatty acids, polyacrylates, polyvinyl alcohol and polyvinylpyrrolidone.
- Enzymes are those from the class of proteases, lipases, amylases or their mixtures in question. Their proportion can be 0.2 to 1 wt .-%.
- the enzymes can be adsorbed to carrier substances and / or in coating substances be embedded.
- the salts of Polyphosphoric acids such as 1-hydroxyethane-1,1-diphosphonic acid (HEDP) and Diethylenetriaminepentamethylenephosphonic acid (DTPMP), preferably in Weight amounts of 0.1 to 1.0 wt% are used.
- HEDP 1-hydroxyethane-1,1-diphosphonic acid
- DTPMP Diethylenetriaminepentamethylenephosphonic acid
- Suitable preservatives are, for example, phenoxyethanol, Formaldehyde solution, parabens, pentanediol or sorbic acid.
- glycol distearic acid esters such as Ethylene glycol distearate, but also fatty acid monoglycol esters.
- salts or adjusting agents for example, sodium sulfate, sodium carbonate or sodium silicate (water glass) are used.
- further additives include sodium borate, starch, sucrose, polydextrose, stilbene compounds, methylcellulose, toluenesulfonate, cumene sulfonate, soaps and silicones.
- the agents according to the invention are usually at a pH in the range from 2 to 12, preferably adjusted to pH 2.1 to 7.8, particularly preferably 2.2 to 6.5.
- hydrophobically modified Acryloyldimethyltaurat containing copolymers in an amount of 0.01 to 10 wt .-% used. Preference is given to an amount of from 0.1 to 5% by weight worked. Particularly preferred is the range of 0.2 to 2 wt .-%. Depending on used amount of polymer, the viscosity of the resulting gels between 100 and 100,000 mPas lie.
- Liquid cleansing gels containing water / organic solvent mixtures The thickening of organic solvents, especially alcohols, in combination with anionic and nonionic surfactants and others Formulation ingredients is modified by the use of hydrophobic, Acryloyldimethyltaurat containing copolymers easily possible. restrictive It must be noted that only water-compatible organic solvents within the meaning of the invention. As non-limiting examples, ethanol, Propanol, isopropanol, DMSO, NMP, acetone, methanol and butanol called become. The resulting gels may contain between 0.1 and 90% by weight of organic Contain solvent. Preference is given to a proportion of 5 to 80 wt .-%.
- gels containing organic solvents from 20 to 60% by weight.
- hydrophobically modified Acryloyldimethyltaurat containing copolymers in these formulations in one Amount of 0.01 to 10 wt .-% used. Preference is given to an amount of 0.1 worked to 5 wt .-%. Particularly preferred is the range of 0.2 to 2 wt .-%.
- the viscosities of the resulting detergent gels containing organic solvents vary between 100 and 100,000 mPas, depending on used amount of polymer.
- Possible Fields of use according to the invention are, for example, bathroom cleaners, glass cleaners, and Floor cleaner.
- Disinfection gels play a major role in the hygiene sector and enjoy the Market for some years rising obesity.
- Specially gels in use as "liquid toilet blocks” are in the sanitary area for years on the Rise.
- aqueous disinfectant solutions by conventional thickeners based on cellulose ethers or polyacrylic acids sometimes requires a high Use concentration of these polymers and is also on the neutral to weak acidic pH range limited.
- hydrophobically modified copolymers containing acryloyldimethyltaurate are used in an amount of from 0.01 to 10% by weight. Preference is given to working with an amount of 0.1 to 5 wt .-%. Particularly preferred is the range of 0.2 to 2 wt .-%. Depending on the amount of polymer used, the viscosity of the resulting gels can be between 100 and 100,000 mPas. Thickening of acid peroxide-containing solutions with hydrophobically modified acryloyldimethyltaurate polymers
- Formulations according to the invention may contain organic or inorganic peroxides, in particular hydrogen peroxide or a mixture thereof.
- organic or inorganic peroxides in particular hydrogen peroxide or a mixture thereof.
- solutions of peroxide with conventional thickeners are difficult to thicken or stabilize over an extended period of time. The reason lies in the fact that a hydrogen peroxide solution is already comparatively unstable at neutral or only slightly acidic pH values. In the decay, the thickeners are attacked and the viscosity decreases over time greatly. In addition, there is a significant loss of hydrogen peroxide activity.
- Bleaching solutions eg for cleaning laundry (liquid stain salt) or dishes: A solution of 0.1 to 30% ww H 2 O 2 , preferably from 1 to 15% ww, particularly preferably from 3 to 10% ww can be thickened by means of inventive hydrophobically modified acryloyldimethyltaurate polymers at pH values ⁇ 5. Even at elevated storage temperatures, a stable viscosity over months is found. The thickening of the bleaching solution makes it easier for the user to set the optimal dosage. The solution does not splash and the handling is safer.
- Peroxide-containing cleaners can, for. B. in the field of cleaning hard surfaces in Hygiene or sanitary area are used. In this case, you can Formulations are also prepared which include anionic and nonionic surfactants contain. Very useful are such agents, for example for the cleaning of Toilets.
- the peroxide-based cleaner adheres to the ceramic and can so his optimally develop cleansing and disinfecting effects.
- Polymer A is poly [acryloyldimethyltauric acid ammonium salt-co-Genapol T-250 methacrylate-co-trimethylolpropane trimethacrylate], Mw 570,000 g / mol.
- Polymer B is poly [acryloyldimethyltaurate sodium salt co-Genapol 070 acrylate], Mw 1,000,000 g / mol.
- Polymer C is poly [acryloyldimethyltauric acid ammonium salt-co-vinylformamide-co-MPEG 750-methacrylate-co-trimethylolpropane triacrylate], Mw 1,500,000 g / mol.
- All formulations also contain, as needed, Preservative, dye and / or perfume.
- Typical viscosities of highly concentrated formulations are in the range of 700 - 1000 mPas, typical viscosities of gels are in the range of 2000 - 3000 mPas.
- Liquid Bleach Booster are added to the detergent in the Washer dosed to improve stain removal. She can also be used for pre-treatment directly on the fabric on the stain be applied. The higher viscosity belies a higher one Activity before. For direct order can also be a more targeted application be enabled.
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Abstract
Description
Die vorliegende Erfindung betrifft flüssige Wasch-, Reinigungs-, Desinfektions- und Bleichmittel, enthaltend hydrophob modifizierte Copolymere auf Basis von Acryloyldimethyltaurinsäure. Die fertigen Formulierungen zeichnen sich durch ein günstiges rheologisches Verhalten, sowie durch eine gute Kompatibilität mit anderen Komponenten aus. Sie weisen eine hohe Lagerstabilität, insbesondere hohe Stabilität hydrolyseempfindlicher Komponenten, beispielsweise Oxidationsmittel in den Formulierungen, bevorzugt in sauren Formulierungen auf und sind UV stabil.The present invention relates to liquid washing, cleaning, disinfecting and Bleaching agents containing hydrophobically modified copolymers based on Acryloyidimethyltaurine. The finished formulations are characterized by a favorable rheological behavior, as well as good compatibility with others Components off. They have a high storage stability, especially high Stability of hydrolysis-sensitive components, for example oxidizing agents in the formulations, preferably in acidic formulations and are UV stable.
An moderne flüssige Wasch- Reinigungs- und Desinfektionsmittel werden hohe Ansprüche gestellt, die eng mit der Rheologie der Produkte verknüpft sind: Sie müssen neben einem guten und raschen Reinigungsvermögen gegenüber Schmutz und Fett bzw. Desinfektionsvermögen anwendungsfreundlich, sicher, sehr gut hautverträglich, aber auch umweltverträglich sein. Zur Verbesserung der Handhabung für den Verbraucher und des Erscheinungsbildes kommen zunehmend flüssige Produkte mit höheren Viskositäten in den Handel, so dass Verdickern und Gelbildnern eine tragende Rolle zukommt.Modern liquid detergents, cleaners and disinfectants become high Claims that are closely linked to the rheology of the products: you In addition to good and quick cleaning against dirt and grease or disinfecting power easy to use, safe, very good skin-friendly, but also environmentally friendly. To improve the Handling for the consumer and the appearance come increasingly liquid products with higher viscosities in the trade, allowing thickeners and Gelbildnern plays a major role.
Als Konsistenzgeber werden bisher fast ausschließlich synthetische oder teilsynthetische Polymere auf Basis von vernetzten Polyacrylsäuren (Carbomere, Carbopole), teilhydrolysierten Polyacrylamide, Celluloseethern, Xanthan oder Guar-Gum verwandt. Dabei tritt immer das Problem der Intoleranz gegenüber niedrigen pH-Werten auf, was die Anwendungsmöglichkeiten vieler Technologien auf den Neutral- bzw. schwach sauren Bereich einschränkt.As a consistency provider are so far almost exclusively synthetic or partially synthetic polymers based on crosslinked polyacrylic acids (carbomers, Carbopols), partially hydrolyzed polyacrylamides, cellulose ethers, xanthan gum or guar gum related. There always occurs the problem of intolerance to low pH levels on what the potential applications of many technologies on the Neutral or weakly acidic range limits.
Aufgabe vorliegender Erfindung war es demzufolge, einen Verdicker für Wasch- und
Reinigungsmittelformulierungen zu finden, der auch im sauren Milieu unter pH 5
seine Wirksamkeit nicht verliert.
Überraschenderweise wurde nun gefunden, dass dieser gravierende Nachteil durch
den Einsatz von hydrophob modifizierten Copolymeren auf Basis von
Acrylolydimethyltaurat, deren Herstellung in EP-A-1 069 142 beschrieben ist,
beseitigt werden kann.Object of the present invention was therefore to find a thickener for washing and cleaning formulations, which does not lose its effectiveness in an acidic environment below pH 5.
Surprisingly, it has now been found that this serious disadvantage can be eliminated by the use of hydrophobically modified copolymers based on acrylolydimethyl taurate, the preparation of which is described in EP-A-1 069 142.
Es ist gelungen mit Hilfe dieser polymeren Strukturen Formulierungen zum Waschen, Reinigen und Desinfizieren auf Viskositäten größer 100 cP einzustellen. In besonderen Ausführungsformen handelt es sich um Formulierungen mit saurem Charakter (pH < 5). Aufgrund des sauren Milieus gelingt es zudem pH-empfindliche Oxidationsmittel wie beispielsweise Wasserstoffperoxid dauerhaft zu stabilisieren und dadurch neuen Anwendungen im Reinigungs- und Hygienebereich zugänglich zu machen. Erfreulicherweise zeichnen sich diese Formulierungen zusätzlich durch eine hohe UV-Stabilität aus. Dies ermöglicht die Verwendung von transparenten Verpackungsmaterialien, die derzeit auf dem Markt sehr gefragt sind.It has been possible with the help of these polymeric structures formulations for Washing, cleaning and disinfecting to viscosities greater than 100 cP. In particular embodiments are formulations with acidic Character (pH <5). Due to the acidic environment, it also manages to be pH-sensitive To stabilize oxidizing agents such as hydrogen peroxide permanently and thus accessible to new applications in the cleaning and hygiene sector close. Fortunately, these formulations are additionally characterized high UV stability. This allows the use of transparent Packaging materials that are currently in great demand in the market.
Gegenstand der Erfindung sind flüssige Wasch-, Reinigungs-, Desinfektions- und
Bleichmittel, enthaltend amphiphile Copolymere, die Struktureinheiten umfassen,
welche abgeleitet sind aus
Comonomere mit mehr als eine polymerisationsfähige Einheit führen zur Vernetzung der erfindungsgemäßen Strukturen.Comonomers with more than one polymerizable unit lead to crosslinking the structures according to the invention.
Die erfindungsgemäßen Copolymere besitzen bevorzugt ein Molekulargewicht Mw von 103 g/mol bis 109 g/mol, besonders bevorzugt von 104 bis 107 g/mol, insbesondere bevorzugt 5·104 bis 5·106 g/mol. Mw ist für die Zwecke dieser Erfindung generell durch GPC gegen Polystyrolsulfonsäure zu bestimmen. The copolymers according to the invention preferably have a molecular weight M w of from 10 3 g / mol to 10 9 g / mol, more preferably from 10 4 to 10 7 g / mol, particularly preferably from 5 × 10 4 to 5 × 10 6 g / mol. M w for the purposes of this invention is generally to be determined by GPC versus polystyrene sulfonic acid.
Bei den Acryloyldimethyltauraten (Struktureinheit a) kann es sich um die anorganischen oder organischen Salze der Acryloyldimethyltaurinsäure handeln. Bevorzugt werden die Li+-, Na+-, K+-, Mg++-, Ca++-, Al+++- und/oder NH4 +-Salze. Ebenfalls bevorzugt sind die Monoalkylammonium-, Dialkylammonium-, Trialkylammonium- und/oder Tetraalkylammoniumsalze, wobei es sich bei den Alkylsubstituenten der Amine unabhängig voneinander um (C1-C22)-Alkylreste handeln kann, die gegebenenfalls mit bis zu 3 (C2-C10)-Hydroxyalkylgruppen besetzt sein können. Weiterhin sind auch ein bis dreifach ethoxylierte Ammoniumverbindungen mit unterschiedlichem Ethoxylierungsgrad bevorzugt. Es sollte angemerkt werden, dass auch Mischungen von zwei oder mehreren der oben genannten Verbindungen erfindungsgemäß sind.The acryloyldimethyltaurates (structural unit a) may be the inorganic or organic salts of acryloyldimethyltaurine acid. Preference is given to the Li + , Na + , K + , Mg ++ , Ca ++ , Al +++ and / or NH 4 + salts. Likewise preferred are the monoalkylammonium, dialkylammonium, trialkylammonium and / or tetraalkylammonium salts, where the alkyl substituents of the amines can independently of one another be (C 1 -C 22 ) -alkyl radicals which are optionally substituted by up to 3 (C 2 -) C 10 ) hydroxyalkyl groups may be occupied. Furthermore, one to three times ethoxylated ammonium compounds with different degrees of ethoxylation are preferred. It should be noted that mixtures of two or more of the above compounds are also within the scope of the invention.
Der Neutralisationsgrad der Acryloyldimethyltaurinsäure kann zwischen 0 und 100 % betragen, besonders bevorzugt ist ein Neutralisationsgrad von oberhalb 80 %.The degree of neutralization of acryloyldimethyltaurine can be between 0 and 100% be particularly preferred is a degree of neutralization of above 80%.
Bezogen auf die Gesamtmasse der Copolymere kann der Gehalt an Acryloyldimethyltaurinsäure bzw. Acryloyldimethyltauraten 0,1 bis 99,9 Gew.-%, bevorzugt 20 bis 99,5 Gew.-%, besonders bevorzugt 50 bis 98 Gew.-% betragen.Based on the total mass of the copolymers, the content of Acryloyldimethyltaurine or acryloyldimethyltaurate 0.1 to 99.9% by weight, preferably 20 to 99.5 wt .-%, particularly preferably 50 to 98 wt .-% amount.
Erfindungsgemäß wird bei der Copolymerisation mindestens ein sogenanntes Makromonomeres (Struktureinheit b) eingesetzt. Es handelt sich bei den Makromonomeren um mindestens einfach olefinisch funktionalisierte Polymere mit einer oder mehreren diskreten Wiederholungseinheiten und einem zahlenmittleren Molekulargewicht größer oder gleich 200 g/mol. Bei der Copolymerisation können auch Mischungen chemisch unterschiedlicher Makromonomere b) eingesetzt werden.According to the invention in the copolymerization at least one so-called Macromonomer (structural unit b) used. It concerns with the Macromonomers to at least single olefinically functionalized polymers with one or more discrete repeating units and one number average Molecular weight greater than or equal to 200 g / mol. In the copolymerization can also mixtures of chemically different macromonomers b) used become.
Bezogen auf die Gesamtmasse der Copolymere kann der Gehalt an Makromonomeren (Struktureinheit b) vorzugsweise 0,1 bis 99,9 Gew.-%, insbesondere 0,5 bis 80 Gew.-%, besonders bevorzugt 2 bis 50 Gew.-% betragen.Based on the total mass of the copolymers, the content of Macromonomers (structural unit b) preferably 0.1 to 99.9 wt .-%, in particular 0.5 to 80 wt .-%, particularly preferably 2 to 50 wt .-% amount.
Bevorzugt als Makromonomere b) sind Verbindungen gemäß Formel (I).
R1 stellt eine polymerisationsfähige Funktion aus der Gruppe der vinylisch ungesättigten Verbindungen dar, die zum Aufbau polymerer Strukturen auf radikalischem Wege geeignet sind. Bevorzugt stellt R1 einen Vinyl-, Allyl-, Methallyl-, Methylvinyl-, Acryl-, Methacryl-, Crotonyl-, Senecionyl-, Itaconyl-, Maleinyl-, Fumaryloder Styrylrest dar.R 1 represents a polymerizable function from the group of vinylically unsaturated compounds, which are suitable for the construction of polymeric structures by free radicals. Preferably, R 1 represents a vinyl, allyl, methallyl, methylvinyl, acrylic, methacrylic, crotonyl, senecionyl, itaconyl, maleinyl, fumarylo or styryl radical.
Zur Anbindung der Polymerkette an die reaktive Endgruppe ist eine geeignete verbrückende Gruppe Y erforderlich. Bevorzugte Brücken Y sind -O-, -C(O)-, - C(O)-O-, -S-, -O-CH2-CH(O-)-CH2OH, -O-CH2-CH(OH)-CH2O-, -O-SO2-O-, - O-SO-O-, -PH-, -P(CH3)-, -PO3-, -NH- und -N(CH3)-, besonders bevorzugt -O-.To attach the polymer chain to the reactive end group, a suitable bridging group Y is required. Preferred bridges Y are -O-, -C (O) -, - C (O) -O-, -S-, -O-CH 2 -CH (O -) - CH 2 OH, -O-CH 2 - CH (OH) -CH 2 O-, -O-SO 2 -O-, -O-SO-O-, -PH-, -P (CH 3 ) -, -PO 3 -, -NH- and -N (CH 3 ) -, more preferably -O-.
Der polymere Mittelteil des Makromonomeren wird durch die diskreten
Wiederholungseinheiten A, B, C und D repräsentiert. Bevorzugte
Wiederholungseinheiten A, B, C und D leiten sich ab von Acrylamid, Methacrylamid,
Ethylenoxid, Propylenoxid, AMPS, Acrylsäure, Methacrylsäure, Methylmethacrylat,
Acrylnitril, Maleinsäure, Vinylacetat, Styrol, 1,3-Butadien, Isopren, Isobuten,
Diethylacrylamid und Diisopropylacrylamid, insbesondere von Ethylenoxid und
Propylenoxid.
Die Indizes v, w, x und z in Formel (I) repräsentieren die stöchiometrische
Koeffizienten betreffend die Wiederholungseinheiten A, B, C und D. v, w, x und z
betragen unabhängig voneinander 0 bis 500, bevorzugt 1 bis 30, wobei die Summe
der vier Koeffizienten im Mittel ≥1 sein muss.The polymeric middle part of the macromonomer is represented by the discrete repeating units A, B, C and D. Preferred repeating units A, B, C and D are derived from acrylamide, methacrylamide, ethylene oxide, propylene oxide, AMPS, acrylic acid, methacrylic acid, methyl methacrylate, acrylonitrile, maleic acid, vinyl acetate, styrene, 1,3-butadiene, isoprene, isobutene, diethylacrylamide and diisopropylacrylamide , in particular of ethylene oxide and propylene oxide.
The indices v, w, x and z in formula (I) represent the stoichiometric coefficients relating to repeating units A, B, C and D. v, w, x and z are independently 0 to 500, preferably 1 to 30, wherein Sum of the four coefficients on average must be ≥1.
Die Verteilung der Wiederholungseinheiten über die Makromonomerkette kann statistisch, blockartig, alternierend oder gradientenartig sein.The distribution of repeating units via the macromonomer chain can be random, block-like, alternating or gradient-like.
R2 bedeutet einen linearen oder verzweigten aliphatischen, olefinischen, cycloaliphatischen, arylaliphatischen oder aromatischen (C1-C50)-Kohlenwasserstoffrest, OH, -NH2, -N(CH3)2 oder ist gleich der Struktureinheit [-Y-R1]. Im Falle von R2 gleich [-Y-R1] handelt es sich um difunktionelle Makromonomere, die zur Vernetzung der Copolymere geeignet sind.R 2 represents a linear or branched aliphatic, olefinic, cycloaliphatic, arylaliphatic or aromatic (C 1 -C 50 ) -hydrocarbon radical, OH, -NH 2 , -N (CH 3 ) 2 or is identical to the structural unit [-YR 1 ]. In the case of R 2 equal to [-YR 1 ] are difunctional macromonomers, which are suitable for crosslinking of the copolymers.
Besonders bevorzugt als Makromonomere b) sind acrylisch- oder methacrylisch monofunktionalisierte Alkylethoxylate gemäß Formel (II). Particularly preferred as macromonomers b) are acrylic or methacrylic monofunctionalized alkyl ethoxylates according to formula (II).
R3, R4, R5 und R6 bedeuten unabhängig voneinander Wasserstoff oder n-aliphatische, iso-aliphatische, olefinische, cycloaliphatische, arylaliphatische oder aromatische (C1-C30)-Kohlenwasserstoffreste.R 3 , R 4 , R 5 and R 6 independently of one another are hydrogen or n-aliphatic, iso-aliphatic, olefinic, cycloaliphatic, arylaliphatic or aromatic (C 1 -C 30 ) -hydrocarbon radicals.
Bevorzugt sind R3 und R4 gleich H oder -CH3, besonders bevorzugt H. R5 ist gleich H oder -CH3, und R6 ist gleich einem n-aliphatischen, iso-aliphatischen, olefinischen, cycloaliphatischen, arylaliphatischen oder aromatischen (C1-C30)-Kohlenwasserstoffrest.R 3 and R 4 are preferably H or -CH 3 , particularly preferably H. R 5 is H or -CH 3 , and R 6 is equal to an n-aliphatic, iso-aliphatic, olefinic, cycloaliphatic, arylaliphatic or aromatic ( C 1 -C 30 ) hydrocarbon radical.
m und n sind wiederum die stöchiometrischen Koeffizienten betreffend die Ethylenoxideinheiten (EO) und Propylenoxideinheiten (PO). m und n betragen unabhängig voneinander 0 bis 500, bevorzugt 1 bis 30, wobei die Summe aus m und n im Mittel ≥1 sein muss. Die Verteilung der EO- und PO-Einheiten über die Makromonomerkette kann statistisch, blockartig, alternierend oder gradientenartig sein. Y steht für die obengenannten Brücken.m and n are again the stoichiometric coefficients concerning the Ethylene oxide units (EO) and propylene oxide units (PO). m and n amount independently 0 to 500, preferably 1 to 30, wherein the sum of m and n must be on average ≥1. The distribution of EO and PO units over the Macromonomer chain can be random, blocky, alternating or gradient-like be. Y stands for the bridges mentioned above.
Insbesondere bevorzugte Makromonomeren haben die folgende Struktur gemäß
Formel (II):
Bevorzugt beträgt das Molekulargewicht der Makromonomeren b) 200 g/mol bis 106 g/mol, besonders bevorzugt 150 bis 104 g/mol und insbesondere bevorzugt 200 bis 5000 g/mol.The molecular weight of the macromonomers b) is preferably 200 g / mol to 10 6 g / mol, more preferably 150 to 10 4 g / mol and particularly preferably 200 to 5000 g / mol.
Als Comonomere c) können alle olefinisch ungesättigten Monomere eingesetzt werden, deren Reaktionsparameter eine Copolymerisation mit Acryloyldimethyltaurinsäure und/oder Acryloyldimethyltauraten in den jeweiligen Reaktionsmedien erlauben.As comonomers c) all olefinically unsaturated monomers can be used whose reaction parameters are copolymerized with Acryloyldimethyltaurinsäure and / or Acryloyldimethyltauraten in the respective Allow reaction media.
Bevorzugt Verwendung finden offenkettige N-Vinylamide, bevorzugt N-Vinylformamid (VIFA), N-Vinylmethylformamid, N-Vinylmethylacetamid (VIMA) und N-Vinylacetamid; cyclischen N-Vinylamide (N-Vinyllactame) mit einer Ringgröße von 3 bis 9, bevorzugt N-Vinylpyrrolidon (NVP) und N-Vinylcaprolactam; Amide der Acrylund Methacrylsäure, bevorzugt Acrylamid, Methacrylamid, N,N-Dimethylacrylamid, N,N-Diethylacrylamid und N,N-Diisopropylacrylamid; alkoxylierte Acryl- und Methacrylamide, bevorzugt Hydroxyethylmethacrylat, Hydroxymethylmethacrylamid, Hydroxyethylmethacrylamid, Hydroxypropylmethacrylamid und Bernsteinsäuremono[2-(methacryloyloxy)ethylester]; N,N-Dimethylaminomethacrylat; Diethylaminomethylmethacrylat; Acryl- und Methacrylamidoglykolsäure; 2- und 4-Vinylpyridin; Vinylacetat; Methacrylsäureglycidylester; Styrol; Acrylnitril; Stearylacrylat; Laurylmethacrylat.Preference is given to using open-chain N-vinylamides, preferably N-vinylformamide (VIFA), N-vinylmethylformamide, N-vinylmethylacetamide (VIMA) and N-vinylacetamide; cyclic N-vinylamides (N-vinyllactams) having a ring size of 3 to 9, preferably N-vinylpyrrolidone (NVP) and N-vinylcaprolactam; Amides of acrylic and Methacrylic acid, preferably acrylamide, methacrylamide, N, N-dimethylacrylamide, N, N-diethylacrylamide and N, N-diisopropylacrylamide; alkoxylated acrylic and Methacrylamides, preferably hydroxyethyl methacrylate, hydroxymethylmethacrylamide, Hydroxyethyl methacrylamide, hydroxypropyl methacrylamide and succinic acid mono [2- (methacryloyloxy) ethyl ester]; N, N-dimethylaminomethacrylate; diethylaminomethyl; Acrylic and methacrylamidoglycolic acid; 2- and 4-vinylpyridine; vinyl acetate; methacrylate; styrene; acrylonitrile; stearyl; Lauryl.
Zusätzlich können eine oder mehrere ungesättigte Carbonsäuren bzw. deren Salze in die Struktur einpolymerisiert sein. Insbesondere bevorzugt sind Acrylsäure, Methacrylsäure, Styrolsulfonsäure, Maleinsäure, Fumarsäure, Crotonsäure, Itaconsäure und Seneciosäure.In addition, one or more unsaturated carboxylic acids or their salts be polymerized into the structure. Particularly preferred are acrylic acid, Methacrylic acid, styrenesulfonic acid, maleic acid, fumaric acid, crotonic acid, Itaconic acid and senecioic acid.
Als Gegenionen der Säuren bevorzugt sind Li+, Na+, K+, Mg++, Ca++, Al+++, NH4 +, Monoalkylammonium-, Dialkylammonium-, Trialkylammonium- und/oder Tetraalkylammoniumreste, wobei es sich bei den Alkylsubstituenten der Amine unabhängig voneinander um (C1-C22)-Alkylreste handeln kann, die gegebenenfalls mit bis zu 3 (C2-C10)-Hydroxyalkylgruppen besetzt sein können. Zusätzlich können auch ein bis dreifach ethoxylierte Ammoniumverbindungen mit unterschiedlichem Ethoxylierungsgrad Anwendung finden. Der Neutralisationsgrad der Carbonsäuren kann zwischen 0 und 100 % betragen.Preferred as counterions of the acids are Li + , Na + , K + , Mg ++ , Ca ++ , Al +++ , NH 4 + , monoalkylammonium, dialkylammonium, trialkylammonium and / or tetraalkylammonium radicals, it being the case with the Alkyl substituents of the amines independently of one another can be (C 1 -C 22 ) -alkyl radicals, which may optionally be occupied by up to 3 (C 2 -C 10 ) -hydroxyalkyl groups. In addition, it is also possible to use one to three times ethoxylated ammonium compounds having a different degree of ethoxylation. The degree of neutralization of the carboxylic acids can be between 0 and 100%.
In einer weiteren Ausführungsform sind die erfindungsgemäßen Copolymere vernetzt, d.h. sie enthalten Comonomere (Struktureinheit c) mit mindestens zwei polymerisationsfähigen Vinylgruppen.In a further embodiment, the copolymers according to the invention are crosslinked, i. they contain comonomers (structural unit c) with at least two polymerizable vinyl groups.
Bevorzugte Vernetzer sind Methylenbisacrylamid; Methylenbismethacrylamid; Ester
ungesättigter Mono- und Polycarbonsäuren mit Polyolen, bevorzugt Diacrylate und
Triacrylate bzw. -methacrylate, besonders bevorzugt Butandiol- und
Ethylenglykoldiacrylat bzw. -methacrylat, Trimethylolpropantriacrylat (TMPTA) und
Allylverbindungen, bevorzugt Allyl(meth)acrylat, Triallylcyanurat,
Maleinsäurediallylester, Polyallylester, Tetraallyloxyethan, Triallylamin,
Tetraallylethylendiamin; Allylester der Phosphorsäure; und/oder
Vinylphosphonsäurederivate.
Besonders bevorzugt als Vernetzer ist Trimethylolpropantriacrylat (TMPTA) und
Timethylolpropantrimethacrylat (TMPTMA).Preferred crosslinkers are methylenebisacrylamide; methylenebismethacrylamide; Esters of unsaturated mono- and polycarboxylic acids with polyols, preferably diacrylates and triacrylates or methacrylates, more preferably butanediol and ethylene glycol diacrylate or methacrylate, trimethylolpropane triacrylate (TMPTA) and allyl compounds, preferably allyl (meth) acrylate, triallyl cyanurate, maleic acid diallyl ester, polyallyl ester, tetraallyloxyethane , Triallylamine, tetraallylethylenediamine; Allyl ester of phosphoric acid; and / or vinylphosphonic acid derivatives.
Particularly preferred crosslinkers are trimethylolpropane triacrylate (TMPTA) and timethylolpropane trimethacrylate (TMPTMA).
Mischungen von einfach vinylisch ungesättigten Comonomeren mit mehrfach ungesättigten Comonomeren (Vernetzer) sind ebenfalls erfindungsgemäß.Mixtures of monounsaturated vinyl comonomers with multiple unsaturated comonomers (crosslinkers) are also according to the invention.
Der Gewichtsanteil der Comonomeren (Struktureinheit c), bezogen auf die Gesamtmasse der erfindungsgemäßen Copolymere, beträgt bevorzugt 0,01 bis 90 Gew.-%, besonders bevorzugt 0,05 bis 50 Gew.-% und insbesondere bevorzugt 0,1 bis 40 Gew.-%.The proportion by weight of comonomers (structural unit c), based on the Total mass of the copolymers of the invention is preferably from 0.01 to 90 wt .-%, particularly preferably 0.05 to 50 wt .-% and particularly preferably 0.1 to 40 wt .-%.
Als Polymerisationsmedium können alle organischen oder anorganischen Lösungsmittel dienen, die sich bezüglich radikalischer Polymerisationsreaktionen weitestgehend inert verhalten und vorteilhafterweise die Bildung mittlerer oder hoher Molekulargewichte zulassen. Bevorzugt Verwendung finden Wasser, niedere Alkohole, bevorzugt Methanol, Ethanol, Propanole, iso-, sec.- und t-Butanol, insbesondere bevorzugt t-Butanol, Kohlenwasserstoffe mit 1 bis 30 Kohlenstoffatomen und Mischungen der vorgenannten Verbindungen.As a polymerization medium, all organic or inorganic Solvents that are concerned with radical polymerization reactions largely inert behavior and advantageously the formation of medium or high Allow molecular weights. Preferably use find water, lower Alcohols, preferably methanol, ethanol, propanols, iso-, sec- and t-butanol, especially preferred is t-butanol, hydrocarbons having 1 to 30 Carbon atoms and mixtures of the aforementioned compounds.
Die Polymerisationsreaktion erfolgt bevorzugt im Temperaturbereich zwischen 0 und 150°C, besonders bevorzugt zwischen 10 und 100°C, sowohl bei Normaldruck als auch unter erhöhtem oder erniedrigtem Druck. Gegebenenfalls kann die Polymerisation auch unter einer Schutzgasatmosphäre, vorzugsweise unter Stickstoff, ausgeführt werden.The polymerization reaction preferably takes place in the temperature range between 0 and 150 ° C, more preferably between 10 and 100 ° C, both at atmospheric pressure as even under increased or reduced pressure. If necessary, the Polymerization also under a protective gas atmosphere, preferably below Nitrogen, to be carried out.
Zur Auslösung der Polymerisation können energiereiche elektromagnetische Strahlen, mechanische Energie oder die üblichen chemischen Polymerisationsinitiatoren, wie organische Peroxide, z.B. Benzoylperoxid, tert.-Butylhydroperoxid, Methylethylketonperoxid, Cumolhydroperoxid, Dilauroylperoxid (DLP) oder Azoinitiatoren, wie z.B. Azodiisobutyronitril (AIBN) verwendet werden. Ebenfalls geeignet sind anorganische Peroxyverbindungen, wie z.B. (NH4)2S2O8, K2S2O8 oder H2O2, gegebenenfalls in Kombination mit Reduktionsmitteln (z.B. Natriumhydrogensulfit, Ascorbinsäure, Eisen(II)-sulfat etc.) oder Redoxsystemen, welche als reduzierende Komponente eine aliphatische oder aromatische Sulfonsäure (z.B. Benzolsulfonsäure, Toluolsulfonsäure etc.) enthalten.To initiate the polymerization, high-energy electromagnetic radiation, mechanical energy or the usual chemical polymerization initiators, such as organic peroxides, for example benzoyl peroxide, tert-butyl hydroperoxide, methyl ethyl ketone peroxide, cumene hydroperoxide, dilauroyl peroxide (DLP) or azo initiators, such as azodiisobutyronitrile (AIBN) can be used. Also suitable are inorganic peroxy compounds, such as (NH 4 ) 2 S 2 O 8 , K 2 S 2 O 8 or H 2 O 2 , optionally in combination with reducing agents (eg sodium hydrogen sulfite, ascorbic acid, iron (II) sulfate, etc.) or redox systems containing as reducing component an aliphatic or aromatic sulfonic acid (eg benzenesulfonic acid, toluenesulfonic acid etc.).
Die Polymerisationsreaktion kann z.B. als Fällungspolymerisation, Emulsionspolymerisation, Substanzpolymerisation, Lösungspolymerisation oder Gelpolymerisation geführt. Besonders vorteilhaft für das Eigenschaftsprofil der erfindungsgemäßen Copolymere ist die Fällungspolymerisation, bevorzugt in tert.-Butanol.The polymerization reaction may e.g. as precipitation polymerization, Emulsion polymerization, bulk polymerization, solution polymerization or Gel polymerization led. Particularly advantageous for the property profile of Copolymers of the invention is the precipitation polymerization, preferably in tert-butanol.
Erfindungsgemäß können die oben beschriebenen hydrophob modifizierten Copolymere auf Basis von Acryloyldimethyltaurat generell in allen Wasch-, Reinigungs-, Desinfektions- und Bleichmitteln jeder Art eingesetzt werden. Bevorzugt werden sie eingesetzt als Verdicker in sauren Reinigungsmittelformulierungen für harte Oberflächen aus Keramik, Metall, Glas oder Kunststoff, beispielsweise in flüssigen Allzweckreinigern, im Sanitärbereich, beispielsweise Flüssigtoilettenstein, kalklösender Badreinigern, aber auch Geschirrspülmitteln. Des weiteren sind sie geeignet für den Einsatz in Fleckensalzmittel, Flüssigwaschmitteln und Wäschebleichmittel.According to the invention, the above-described hydrophobically modified Copolymers based on acryloyldimethyltaurate generally in all wash, Cleaning, disinfecting and bleaching agents of any kind are used. They are preferably used as thickeners in acidic Detergent formulations for hard surfaces of ceramic, metal, glass or plastic, for example in liquid all-purpose cleaners, in the sanitary sector, For example, liquid toilet block, limesolvent bath cleaners, but also Dishwashing detergents. Furthermore, they are suitable for use in Stain removers, liquid detergents and laundry bleaches.
Die erfindungsgemäßen Wasch- Reinigungs-, Desinfektions-, und Bleichmittel können in Form von wässrigen, wässrig/organischen, insbesondere wässrig/alkoholischen und organischen Formulierungen vorliegen. Weitere Ausführungsformen können sein: Emulsionen, Dispersionen, Gele und Suspensionen.The washing, cleaning, disinfecting and bleaching agents according to the invention may be in the form of aqueous, aqueous / organic, in particular aqueous / alcoholic and organic formulations are present. Further Embodiments may be: emulsions, dispersions, gels and Suspensions.
In einer bevorzugten Ausführungsform enthalten die erfindungsgemäßen Wasch-,
Reinigungs-, Desinfektions- und Bleichmittel eine saure Komponente.
In Betracht kommen organische oder anorganische Säuren, bevorzugt organische
Säuren, insbesondere bevorzugt alpha-Hydroxysäuren und Säuren ausgewählt aus
Glykolsäure, Milchsäure, Zitronensäure, Weinsäure, Mandelsäure, Salicylsäure,
Ascorbinsäure, Brenztraubensäure, Oligooxa Mono- und Dicarbonsäuren,
Fumarsäure, Retinoesäure, aliphatische und organische Sulfonsäuren,
Benzoesäure, Kojisäure, Fruchtsäure, Äpfelsäure, Gluconsäure, Galacturonsäure,
saure Pflanzen- und/oder Fruchtextrakte und deren Derivate.In a preferred embodiment, the washing, cleaning, disinfecting and bleaching agents according to the invention contain an acidic component.
Suitable organic or inorganic acids, preferably organic acids, more preferably alpha-hydroxy acids and acids selected from glycolic, lactic, citric, tartaric, mandelic, salicylic, ascorbic, pyruvic, oligooxa mono- and dicarboxylic, fumaric, retinoic, aliphatic and organic Sulfonic acids, benzoic acid, kojic acid, fruit acid, malic acid, gluconic acid, galacturonic acid, acidic plant and / or fruit extracts and their derivatives.
Des weiteren können bevorzugte Ausführungsformen Oxidationsmittel, insbesondere Wasserstoffperoxid oder dessen Additionsverbindungen, beispielsweise die Additionsverbindungen von Wasserstoffperoxid an Harnstoff, Melamin oder Natriumborat enthalten oder Lösungen von Perborat oder Percarbonat gegebenenfalls auch Caroat enthalten.Furthermore, preferred embodiments may include oxidizing agents, in particular Hydrogen peroxide or its addition compounds, for example the Addition compounds of hydrogen peroxide to urea, melamine or Sodium borate or solutions of perborate or percarbonate optionally also contain caroate.
Die erfindungsgemäßen Zubereitungen können Oxidationsmittel in Mengen von 0,1 bis 30 Gew.-%, besonders bevorzugt 0,5 bis 18 Gew.-%, insbesondere 1,5 bis 9 Gew.-% enthalten.The preparations according to the invention may contain oxidizing agents in amounts of 0.1 to 30 wt .-%, particularly preferably 0.5 to 18 wt .-%, in particular 1.5 to 9 wt .-% included.
Die erfindungsgemäßen Wasch-, Reinigungs-, Desinfektions- und Bleichmittel können Tenside nichtionischer, anionischer, kationischer oder amphoterer Natur sowie übliche Hilfs- und Zusatzstoffe in unterschiedlichen Mengen enthalten.The washing, cleaning, disinfecting and bleaching agents according to the invention may be surfactants of nonionic, anionic, cationic or amphoteric nature and customary auxiliaries and additives in different amounts.
Bevorzugte nichtionische Tenside sind Fettalkoholoxethylate mit ca. 1 bis ca. 25 mol Ethylenoxid. Die Alkylkette der aliphatischen Alkohole kann linear oder verzweigt, primär oder sekundär sein, und enthält im allgemeinen von 8 bis 22 Kohlenstoffatome. Besonders bevorzugt sind die Kondensationsprodukte von Alkoholen, die eine Alkylkette von 10 bis 20 Kohlenstoffen enthalten, mit 2 bis 18 mol Ethylenoxid pro mol Alkohol. Die Alkylkette kann gesättigt oder auch ungesättigt sein. Ebenso können die Alkoholethoxylate eine enge Homologenverteilung des Ethylenoxides ("Narrow Range Ethoxylates") oder eine breite Homologenverteilung des Ethylenoxides ("Broad Range Ethoxylates") aufweisen. Beispiele von kommerziell erhältlichen nichtionischen Tensiden dieses Types sind Tergitol™ 15-S-9 (Kondensationsprodukt eines C11-C15 linearen sekundären Alkohols mit 9 mol Ethylenoxid), Tergitol™ 24-L-NMW (Kondensationsprodukt eines C12-C14linearen primären Alkohols mit 6 mol Ethylenoxid mit enger Molgewichtsverteilung). Ebenfalls unter diese Produktklasse fallen die Genapol™-Marken der Clariant GmbH.Preferred nonionic surfactants are fatty alcohol ethoxylates containing from about 1 to about 25 moles of ethylene oxide. The alkyl chain of the aliphatic alcohols may be linear or branched, primary or secondary, and generally contains from 8 to 22 carbon atoms. Particularly preferred are the condensation products of alcohols containing an alkyl chain of 10 to 20 carbons with 2 to 18 moles of ethylene oxide per mole of alcohol. The alkyl chain can be saturated or unsaturated. Likewise, the alcohol ethoxylates may have a narrow homolog distribution of the ethylene oxide ("narrow range ethoxylates") or a broad homolog distribution of the ethylene oxide ("broad range ethoxylates"). Examples of commercially available nonionic surfactants of this type are Tergitol ™ 15-S-9 (condensation product of a C 11 -C 15 linear secondary alcohol with 9 moles of ethylene oxide), Tergitol ™ 24-L NMW (condensation product of a C 12 -C 14 linear primary Alcohol with 6 moles of ethylene oxide with narrow molecular weight distribution). Also included in this product class are the Genapol ™ brands from Clariant GmbH.
Darüber hinaus kommen erfindungsgemäß auch andere bekannte Typen von nichtionischen Tensiden in Frage, wie Polyethylen-, Polypropylen- und Polybutylenoxidaddukte von Alkylphenolen mit 6 bis 12 C-Atomen in der Alkylkette, Additionsprodukte von Ethylenoxid mit einer hydrophoben Base, gebildet aus der Kondensation von Propylenoxid mit Propylenglykol oder Additionsprodukte von Ethylenoxid mit einem Reaktionsprodukt von Propylenoxid und Ethylendiamin.In addition, according to the invention, other known types of nonionic surfactants such as polyethylene, polypropylene and Polybutylene oxide adducts of alkylphenols having 6 to 12 C atoms in the alkyl chain, Addition products of ethylene oxide with a hydrophobic base formed from the Condensation of propylene oxide with propylene glycol or addition products of Ethylene oxide with a reaction product of propylene oxide and ethylenediamine.
Des weiteren können semipolare nichtionische Tenside, beispielsweise
Aminoxide der Formel III
eingesetzt werden, worin R8 eine Alkyl-, Hydroxyalkyl- oder Alkylphenolgruppe oder
Mischungen hiervon darstellt mit einer Kettenlänge von 8 bis 22 Kohlenstoffatome;
R9 ist eine Alkylen- oder Hydroxyalkylengruppe mit 2 bis 3 Kohlenstoffatomen oder
Mischungen hiervon; R10 ist eine Alkyl- oder Hydroxyalkylgruppe mit 1 bis 3
Kohlenstoffatomen oder eine Polyethylenoxidgruppe mit 1 bis 3
Ethylenoxideinheiten. Die R10/R9-Gruppen können miteinander über ein Sauerstoffoder
Stickstoffatom verbunden sein und somit einen Ring bilden.
Diese Aminoxide umfassen besonders C10-C18-Alkyldimethylaminoxide und C8-C12-Alkoxyethyl-Dihydroxyethylaminoxide.Furthermore, semipolar nonionic surfactants, for example amine oxides of the formula III where R 8 is an alkyl, hydroxyalkyl or alkylphenol group or mixtures thereof having a chain length of 8 to 22 carbon atoms; R 9 is an alkylene or hydroxyalkylene group having 2 to 3 carbon atoms or mixtures thereof; R 10 is an alkyl or hydroxyalkyl group having 1 to 3 carbon atoms or a polyethylene oxide group having 1 to 3 ethylene oxide units. The R 10 / R 9 groups may be linked together via an oxygen or nitrogen atom and thus form a ring.
These amine oxides particularly include C 10 -C 18 alkyl dimethyl amine oxides and C 8 -C 12 alkoxyethyl dihydroxyethyl amine oxides.
Anstelle oder zusätzlich zu den nichtionischen Tensiden können die erfindungsgemäßen Mischungen auch anionische Tenside enthalten.Instead of or in addition to the nonionic surfactants, the mixtures according to the invention also contain anionic surfactants.
Als anionische Tenside kommen in Betracht vor allem geradkettige und verzweigte Alkylsulfate, -sulfonate, -carboxylate, -phosphate, Alkylestersulfonate, Arylalkylsulfonate, Alkylethersulfate und Mischungen aus den genannten Verbindungen. Im folgenden sollen einige der in Frage kommenden Typen von anionischen Tensiden näher beschrieben werden.Suitable anionic surfactants are, in particular, straight-chain and branched Alkyl sulfates, sulfonates, carboxylates, phosphates, alkyl ester sulfonates, Arylalkylsulfonate, alkyl ether sulfates and mixtures of the above Links. The following are some of the candidate types of anionic surfactants are described in more detail.
Alkylestersulfonate stellen lineare Ester von C8-C20-Carboxylsäuren (d.h. Fettsäuren) dar, die durch SO3 sulfoniert werden, wie in "The Journal of the American Oil Chemists Society", 52 (1975), pp. 323-329 beschrieben. Geeignete Ausgangsmaterialien sind natürliche Fettderivate, wie z.B. Talg- oder Palmölfettsäure. Alkyl ester sulfonates are linear esters of C 8 -C 20 carboxylic acids (ie, fatty acids) that are sulfonated by SO 3 , as described in The Journal of the American Oil Chemists Society, 52 (1975), pp. 323-329. Suitable starting materials are natural fatty derivatives, such as tallow or palm oil fatty acid.
Alkylsulfate sind wasserlösliche Salze oder Säuren der Formel ROSO3M, worin R bevorzugt einen C10-C24-Kohlenwasserstoffrest, bevorzugt einen Alkyl- oder Hydroxyalkylrest mit 10 bis 20 C-Atomen, besonders bevorzugt einen C12-C18-Alkyloder Hydroxyalkylrest darstellt. M ist Wasserstoff oder ein Kation, z.B. ein Alkalimetallkation (z.B. Natrium, Kalium, Lithium) oder Ammonium oder substituiertes Ammonium, z.B. ein Methyl-, Dimethyl- und Trimethylammoniumkation oder ein quaternäres Ammoniumkation, wie Tetramethylammonium- und Dimethylpiperidiniumkation und quartäre Ammoniumkationen, abgeleitet von Alkylaminen wie Ethylamin, Diethylamin, Triethylamin und deren Mischungen. Alkylketten mit C12-C16 sind dabei bevorzugt für niedrige Waschtemperaturen (z.B. unter ca. 50°C) und Alkylketten mit C16-C18 bevorzugt für höhere Waschtemperaturen (z.B. oberhalb ca. 50°C).Alkyl sulfates are water-soluble salts or acids of the formula ROSO 3 M, wherein R is preferably a C 10 -C 24 -hydrocarbon radical, preferably an alkyl or hydroxyalkyl radical having 10 to 20 C-atoms, particularly preferably a C 12 -C 18 -alkyl or hydroxyalkyl radical , M is hydrogen or a cation, for example an alkali metal cation (eg sodium, potassium, lithium) or ammonium or substituted ammonium, for example a methyl, dimethyl and trimethylammonium cation or a quaternary ammonium cation, such as tetramethylammonium and dimethylpiperidinium cation and quaternary ammonium cations, derived from alkylamines such as ethylamine, diethylamine, triethylamine and mixtures thereof. Alkyl chains with C 12 -C 16 are preferred for low washing temperatures (eg below about 50 ° C) and alkyl chains with C 16 -C 18 preferably for higher washing temperatures (eg above about 50 ° C).
Die Alkylethersulfate sind wasserlösliche Salze oder Säuren der Formel RO(A)mSO3M, worin R einen unsubstituierten C10-C24-Alkyl- oder Hydroxyalkylrest mit 10 bis 24 C-Atomen, bevorzugt einen C12-C20-Alkyl- oder Hydroxyalkylrest, besonders bevorzugt einen C12-C18-Alkyl- oder Hydroxyalkylrest darstellt. A ist eine Ethoxy- oder Propoxyeinheit, m ist eine Zahl von größer als 0, typischerweise zwischen ca. 0,5 und ca. 6, besonders bevorzugt zwischen ca. 0,5 und ca. 3 und M ist ein Wasserstoffatom oder ein Kation wie z.B. ein Metallkation (z.B. Natrium, Kalium, Lithium, Calcium, Magnesium, etc.), Ammonium oder ein substituiertes Ammoniumkation. Beispiele für substituierte Ammoniumkationen sind Methyl-, Dimethyl-, Trimethylammonium- und quaternäre Ammoniumkationen wie Tetramethylammonium und Dimethylpiperidiniumkationen, sowie solche, die von Alkylaminen, wie Ethylamin, Diethylamin, Triethylamin, Mischungen davon und ähnliche, abgeleitet sind. Als Beispiele seien genannt C12-C18-Alkyl-polyethoxylat(1,0)-sulfat, C12-C18-Alkyl-polyethoxylat (2,25)sulfat, C12-C18-Alkyl-polyethoxylat (3,0)sulfat, C12-C18-Alkyl-polyethoxylat (4,0)sulfat, wobei das Kation Natrium oder Kalium ist.The alkyl ether sulfates are water-soluble salts or acids of the formula RO (A) m SO 3 M, where R is an unsubstituted C 10 -C 24 -alkyl or hydroxyalkyl radical having 10 to 24 C atoms, preferably a C 12 -C 20 -alkyl radical. or hydroxyalkyl radical, particularly preferably a C 12 -C 18 -alkyl or hydroxyalkyl radical. A is an ethoxy or propoxy moiety, m is a number greater than 0, typically between about 0.5 and about 6, more preferably between about 0.5 and about 3, and M is a hydrogen atom or a cation such as for example, a metal cation (eg, sodium, potassium, lithium, calcium, magnesium, etc.), ammonium, or a substituted ammonium cation. Examples of substituted ammonium cations are methyl, dimethyl, trimethylammonium and quaternary ammonium cations such as tetramethylammonium and dimethylpiperidinium cations, as well as those derived from alkylamines such as ethylamine, diethylamine, triethylamine, mixtures thereof and the like. Examples which may be mentioned are C 12 -C 18 -alkyl polyethoxylate (1.0) sulfate, C 12 -C 18 -alkyl polyethoxylate (2,25) sulfate, C 12 -C 18 -alkyl polyethoxylate (3.0 ) sulfate, C 12 -C 18 alkyl polyethoxylate (4.0) sulfate, wherein the cation is sodium or potassium.
Andere anionische Tenside die nützlich für den Einsatz in Wasch- und Reinigungsmitteln sind, sind C8-C24-Olefinsulfonate, sulfonierte Polycarboxylsäuren, hergestellt durch Sulfonierung der Pyrolyseprodukte von Erdalkalimetallcitraten, wie z.B. beschrieben im britischen Patent GB 1,082,179, Alkylglycerinsulfate, Fettacylglycerinsulfate, Oleylglycerinsulfate, Alkylphenolethersulfate, primäre Paraffinsulfonate, Alkylphosphate, Alkyletherphosphate, Isethionate, wie Acylisethionate, N-Acyltauride, Alkylsuccinamate, Sulfosuccinate, Monoester der Sulfosuccinate (besonders gesättigte und ungesättigte C12-C18-Monoester) und Diester der Sulfosuccinate (besonders gesättigte und ungesättigte C12-C18-Diester), Acylsarcosinate, Sulfate von Alkylpolysacchariden wie Sulfate von Alkyloylglycosiden, verzweigte primäre Alkylsulfate und Alkylpolyethoxycarboxylate wie die der Formel RO(CH2CH2)kCH2COO-M+ worin R ein C8-C22Alkyl, k eine Zahl von 0 bis 10 und M ein lösliches Salz bildendes Kation ist. Harzsäuren oder hydrierte Harzsäuren, wie Rosin oder hydriertes Rosin oder Tallölharze und Tallölharzsäuren sind ebenfalls einsetzbar. Weitere Beispiele sind in "Surface Active Agents and Detergents" (Vol. I und II, Schwartz, Perry und Berch) beschrieben. Eine Vielzahl solcher Tenside sind auch im US-Patent 3,929,678 beansprucht.Other anionic surfactants useful in laundry detergents and cleaners are C 8 -C 24 olefin sulfonates, sulfonated polycarboxylic acids prepared by sulfonation of pyrolysis products of alkaline earth metal citrates such as described in British Patent GB 1,082,179, alkyl glycerol sulfates, fatty acyl glycerol sulfates, oleyl glycerol sulfates, Alkylphenol ether sulfates, primary paraffin sulfonates, alkyl phosphates, alkyl ether phosphates, isethionates such as acyl isethionates, N-acyl taurides, alkyl succinamates, sulfosuccinates, monoesters of sulfosuccinates (especially saturated and unsaturated C 12 -C 18 monoesters) and diesters of sulfosuccinates (especially saturated and unsaturated C 12 - C 18 diesters), acyl sarcosinates, sulfates of alkyl polysaccharides such as sulfates of alkyloyl glycosides, branched primary alkyl sulfates and alkyl polyethoxycarboxylates such as those of the formula RO (CH 2 CH 2 ) k CH 2 COO - M + wherein R is C 8 -C 22 alkyl, k a number from 0 to 10 and M a soluble one Salt forming cation is. Resin acids or hydrogenated resin acids such as rosin or hydrogenated rosin or tall oil resins and tall oil rosin acids are also useful. Further examples are described in "Surface Active Agents and Detergents" (Vol. I and II, Schwartz, Perry and Berch). A variety of such surfactants are also claimed in U.S. Patent 3,929,678.
Beispiele für amphotere Tenside, die in den Formulierungen der vorliegenden Erfindung Einsatz finden können, sind vor allem solche, die breit als Derivate von aliphatischen sekundären and tertiären Aminen beschrieben werden, in denen der aliphatische Rest linear oder verzweigt sein kann und in denen einer der aliphatischen Substituenten zwischen. 8 bis 18 Kohlenstoffatome enthält und eine anionische, wasserlösliche Gruppe, wie z.B. Carboxy, Sulfonat, Sulfat, Phosphat oder Phosphonat enthält.Examples of amphoteric surfactants used in the formulations of the present invention Invention can be used, especially those that are widely used as derivatives of aliphatic secondary and tertiary amines are described in which the Aliphatic radical may be linear or branched and in which one of the aliphatic substituents between. Contains 8 to 18 carbon atoms and one anionic, water-soluble group, such as e.g. Carboxy, sulfonate, sulfate, phosphate or phosphonate.
Weitere bevorzugte amphotere Tenside sind Alkyldimethylbetaine, Alkylamidobetaine und Alkyldipolyethoxybetaine mit einem Alkylrest, der linear oder verzweigt sein, mit. 8 bis 22 Kohlenstoffatomen, bevorzugt mit 8 bis 18 Kohlenstoffatomen und besonders bevorzugt mit. 12 bis. 18 Kohlenstoffatomen. Diese Verbindungen werden z.B. von der Clariant GmbH unter dem Handelnamen Genagen® CAB vermarktet.Further preferred amphoteric surfactants are alkyl dimethyl betaines, Alkylamidobetaines and Alkyldipolyethoxybetaine having an alkyl radical which is linear or be branched, with. 8 to 22 carbon atoms, preferably 8 to 18 Carbon atoms and particularly preferably with. 12 to. 18 carbon atoms. These compounds are e.g. from the Clariant GmbH under the trade name Genagen® CAB markets.
Die Wasch- und Reinigungsmittel enthalten, je nach Anwendungszweck, neben den genannten Tensiden noch die jeweils spezifischen Hilfs- und Zusatzstoffe beispielsweise Builder, Salze (Elektrolyte), Bleichmittel, Bleichaktivatoren, optische Aufheller, Komplexbildner, Vergrauungsinhibitoren, Lösungsvermittler, Enzyme, Verdickungsmittel, Konservierungsmittel, Duft- und Farbstoffe, Perlglanzmittel, Schauminhibitoren, Sequestriermittel.The washing and cleaning agents contain, depending on the application, in addition to the mentioned surfactants nor the respectively specific auxiliaries and additives For example, builders, salts (electrolytes), bleaches, bleach activators, optical Brighteners, complexing agents, grayness inhibitors, solubilizers, enzymes, Thickeners, preservatives, perfumes and dyes, pearlescing agents, Foam inhibitors, sequestering agents.
Als organische und anorganische Gerüststoffe eignen sich neutral oder insbesondere alkalisch reagierende Salze, die Calciumionen auszufällen oder komplex zu binden vermögen. Geeignete und insbesondere ökologisch unbedenkliche Buildersubstanzen, wie feinkristalline, synthetische wasserhaltige Zeolithe von Typ NaA, die ein Calciumbindevermögen im Bereich von 100 bis 200 mg CaO/g aufweisen, finden eine bevorzugte Verwendung. In nichtwässrigen Systemen werden bevorzugt Schichtsilikate eingesetzt. Zeolith und die Schichtsilikate können in einer Menge bis zu 20 Gew.-% im Mittel enthalten sein. Brauchbare organische Gerüstsubstanzen sind beispielsweise die bevorzugt in Form ihrer Natriumsalze eingesetzten Percarbonsäuren, wie Citronensäure und Nitriloacetat (NTA), Ethylendiamintetraessigsäure, sofern ein derartiger Einsatz aus ökologischen Gründen nicht zu beanstanden ist. Analog hierzu können auch polymere Carboxylate und deren Salze eingesetzt werden. Hierzu gehören beispielsweise die Salze homopolymerer oder copolymerer Polyacrylate, Polymethyacrylate und insbesondere Copolymere der Acrylsäure mit Maleinsäure, vorzugsweise solche aus 50% bis 10% Maleinsäure und auch Polyvinylpyrrolidon und Urethane. Die relative Molekülmasse der Homopolymeren liegt im allgemeinen zwischen 1000 und 100 000, die der Copolymeren zwischen 2000 und 200 000, vorzugsweise 50 000 bis 120 000, bezogen auf die freie Säure, insbesondere sind auch wasserlösliche Polyacrylate geeignet, die beispielsweise mit etwa 1 % eines Polyallylethers der Sucrose quervernetzt sind und die eine relative Molekülmasse oberhalb einer Million besitzen. Beispiele hierfür sind die unter dem Namen Carbopol 940 und 941 erhältlichen Polymere. Die quervernetzen Polyacrylate werden in Mengen nicht über 1 Gew.-%, vorzugsweise in Mengen von 0,2 bis 0,7 Gew.-% eingesetzt.As organic and inorganic builders are neutral or especially alkaline salts that precipitate calcium ions or to bind complex. Suitable and especially ecological harmless builders, such as fine crystalline, synthetic hydrous Zeolites of type NaA, which have a calcium binding capacity in the range of 100 to 200 mg CaO / g find a preferred use. In non-aqueous Systems phyllosilicates are preferably used. Zeolite and the Layered silicates may be present in an amount of up to 20% by weight on average. Useful organic builders are, for example, those which are preferably in the form their sodium salts used percarboxylic acids, such as citric acid and Nitriloacetate (NTA), ethylenediaminetetraacetic acid, if such use of ecological reasons is not objectionable. Analogous to this can also polymeric carboxylates and their salts are used. These include for example, the salts of homopolymeric or copolymeric polyacrylates, Polymethyacrylate and in particular copolymers of acrylic acid with maleic acid, preferably those of 50% to 10% maleic acid and also polyvinylpyrrolidone and urethanes. The molecular weight of the homopolymers is generally between 1000 and 100,000, that of the copolymers between 2000 and 200,000, preferably 50,000 to 120,000, based on the free acid, in particular also suitable water-soluble polyacrylates, for example, with about 1% of a Polyallylethers of sucrose are cross-linked and have a molecular weight own over one million. Examples are those under the name Carbopol 940 and 941 available polymers. The crosslinked polyacrylates are used in Amounts not exceeding 1% by weight, preferably in amounts of from 0.2 to 0.7 wt .-% used.
Als Elektrolyt enthalten die erfindungsgemäßen Mittel Salze. Bei den Salzen handelt
es sich um heteropolare Verbindungen, an deren Kristallgitter mindestens eine von
Wasserstoff-lonen verschiedene Kationen-Art und mindestens eine von Hydroxidtonen
verschiedene Anionen-Art beteiligt sind. Bevorzugt enthalten die
erfindungsgemäßen Mittel anorganische Salze, besonders bevorzugt Ammoniumoder
Metallsalze, bevorzugt von Halogeniden, Oxiden, Carbonaten,
Hydrogencarbonaten, Phosphaten, Sulfaten, Nitraten, insbesondere bevorzugt
Natriumchlorid; und/oder organische Salze, bevorzugt Ammonium- oder Metallsalze,
bevorzugt der Glykolsäure, Milchsäure, Zitronensäure, Weinsäure, Mandelsäure,
Salicylsäure, Ascorbinsäure, Brenztraubensäure, Fumarsäure, Retinoesäure,
Sulfonsäuren, Benzoesäure, Kojisäure, Fruchtsäure, Äpfelsäure, Gluconsäure,
Galacturonsäure.
Die Salze sind bevorzugt von ein- oder mehrwertigen Säuren und Basen abgeleitet,
bevorzugt von einwertigen Säuren und/oder einwertigen Basen. Besonders
bevorzugt sind Natrium-, Kalium und Ammoniumsalze.
Als Elektrolyt können die Mittel auch Mischungen verschiedener Salze enthalten. Die
Mittel enthalten die Elektrolyte üblicherweise in einer Konzentration von 0,01 bis
50 Gew.-%, bevorzugt 0,1 bis 50 Gew.-%, besonders bevorzugt 0,5 bis 10 Gew.-%.As electrolyte, the agents according to the invention contain salts. The salts are heteropolar compounds whose crystal lattice has at least one cation species other than hydrogen ions and at least one anion species other than hydroxide ions. The agents according to the invention preferably contain inorganic salts, more preferably ammonium or metal salts, preferably halides, oxides, carbonates, bicarbonates, phosphates, sulfates, nitrates, most preferably sodium chloride; and / or organic salts, preferably ammonium or metal salts, preferably glycolic, lactic, citric, tartaric, mandelic, salicylic, ascorbic, pyruvic, fumaric, retinoic, sulfonic, benzoic, kojic, fruit, malic, gluconic, galacturonic.
The salts are preferably derived from mono- or polybasic acids and bases, preferably from monovalent acids and / or monovalent bases. Particularly preferred are sodium, potassium and ammonium salts.
As electrolyte, the agents may also contain mixtures of different salts. The agents usually contain the electrolytes in a concentration of from 0.01 to 50% by weight, preferably from 0.1 to 50% by weight, particularly preferably from 0.5 to 10% by weight.
Die erfindungsgemäßen Mittel können als Schauminhibitoren Fettsäurealkylesteralkoxylate, Organopolysiloxane und deren Gemische mit mikrofeiner, gegebenenfalls silanierter Kieselsäure sowie Paraffine, Wachse, Mikrokristallinwachse und deren Gemische mit silanierter Kieselsäure, enthalten. Mit Vorteil können auch Gemische verschiedener Schauminhibitoren verwendet werden, z.B. solche aus Silikonöl, Paraffinöl oder Wachsen. Vorzugsweise sind Schauminhibitoren an eine granulare, in Wasser lösliche oder dispergierbare Trägersubstanz gebunden.The agents according to the invention can be used as foam inhibitors Fatty acid alkyl ester alkoxylates, organopolysiloxanes and mixtures thereof with microfine, optionally silanized silica and paraffins, waxes, Microcrystalline waxes and their mixtures with silanized silica. With Advantage may also be used mixtures of different foam inhibitors, e.g. those made of silicone oil, paraffin oil or waxes. Preferably Foam inhibitors to a granular, water-soluble or dispersible Vehicle bound.
Die Flüssigwaschmittel können optische Aufheller beispielsweise Derivate der Diaminostilbendisulfonsäure bzw. deren Alkalimetallsalze enthalten, die sich gut in die Dispersion einarbeiten lassen. Der maximale Gehalt an Aufhellern in den erfindungsgemäßen Mitteln beträgt 0,5 Gew.-%, vorzugsweise werden Mengen von 0,02 bis 0,25 Gew.-% eingesetzt.The liquid detergents can optical brighteners, for example derivatives of Diaminostilbendisulfonsäure or their alkali metal salts, which are well in have the dispersion incorporated. The maximum content of brighteners in the inventive compositions is 0.5 wt .-%, preferably amounts of 0.02 to 0.25 wt .-% used.
Die gewünschte Viskosität der Mittel kann durch Zugabe von Wasser und/oder organischen Lösungsmitteln oder durch Zugabe einer Kombination aus organischen Lösungsmitteln und weitere Verdickungsmitteln eingestellt werden. The desired viscosity of the agents can be achieved by adding water and / or organic solvents or by adding a combination of organic Solvents and other thickening agents can be adjusted.
Prinzipiell kommen als organische Lösungsmittel alle ein- oder mehrwertigen
Alkohole in Betracht. Bevorzugt werden Alkohole mit 1 bis 4 Kohlenstoffatomen wie
Methanol, Ethanol, Propanol, Isopropanol, geradkettige und verzweigtes Butanol,
Glycerin und Mischungen aus den genannten Alkoholen eingesetzt. Weitere
bevorzugte Alkohole sind Polyethylenglykole mit einer relativen Molekülmasse unter
2000. Insbesondere ist ein Einsatz von Polyethylenglykol mit einer relativen
Molekülmasse zwischen 200 und 600 und in Mengen bis zu 45 Gew.-% und von
Polyethylenglykol mit einer relativen Molekülmasse zwischen 400 und 600 in
Mengen von 5 bis 25 Gew.-% bevorzugt. Eine vorteilhafte Mischung aus
Lösungsmitteln besteht aus monomerem Alkohol, beispielsweise Ethanol und
Polyethylenglykol im Verhältnis 0,5 : 1 bis 1,2 : 1, wobei die erfindungsgemäßen
Flüssigwaschmittel 8 bis 12 Gew.-% einer solchen Mischung enthalten können.
Weitere geeignete Lösungsmittel sind beispielsweise Triacetin (Glycerintriacetat) und
1-Methoxy-2-propanol.
Als Verdickungsmittel werden bevorzugt gehärtetes Rizinusöl, Salze von
langkettigen Fettsäuren, vorzugsweise in Mengen von 0 bis 5 Gew.-% und
insbesondere in Mengen von 0,5 bis 2 Gew.-%, beispielsweise Natrium-. Kalium-,
Aluminium-, Magnesium- und Titan-Stearate oder die Natrium und/oder KaliumSalze
der Behensäure, sowie Polysaccharide, insbesondere Xanthan-Gum, Guar-Guar,
Agar-Agar, Alginate und Tylosen, Carboxymethylcellulose und
Hydroxyethylcellulose, ferner höhermolekulare Polyethylenglycolmono- und diester
von Fettsäuren, Polyacrylate, Polyvinylalkohol und Polyvinylpyrrolidon eingesetzt.In principle, all mono- or polyhydric alcohols are suitable as organic solvents. Alcohols having 1 to 4 carbon atoms, such as methanol, ethanol, propanol, isopropanol, straight-chain and branched butanol, glycerol and mixtures of the alcohols mentioned are preferably used. More preferred alcohols are polyethylene glycols having a molecular weight less than 2,000. In particular, use of polyethylene glycol having a molecular weight of between 200 and 600 and up to 45% by weight and polyethylene glycol having a molecular weight of between 400 and 600 in amounts of 5 to 25 wt .-% preferred. An advantageous mixture of solvents consists of monomeric alcohol, for example ethanol and polyethylene glycol in a ratio of 0.5: 1 to 1.2: 1, wherein the liquid detergent according to the invention may contain 8 to 12 wt .-% of such a mixture. Other suitable solvents include triacetin (glycerol triacetate) and 1-methoxy-2-propanol.
Preferred thickeners are hardened castor oil, salts of long-chain fatty acids, preferably in amounts of from 0 to 5% by weight and in particular in amounts of from 0.5 to 2% by weight, for example sodium. Potassium, aluminum, magnesium and titanium stearates or the sodium and / or potassium salts of behenic acid, as well as polysaccharides, in particular xanthan gum, guar guar, agar agar, alginates and tyloses, carboxymethyl cellulose and hydroxyethyl cellulose, and also higher molecular weight polyethylene glycol mono- and diesters of fatty acids, polyacrylates, polyvinyl alcohol and polyvinylpyrrolidone.
Als Enzyme kommen solche aus der Klasse der Proteasen, Lipasen, Amylasen bzw. deren Gemische in Frage. Ihr Anteil kann 0,2 bis 1 Gew.-% betragen. Die Enzyme können an Trägersubstanzen adsorbiert werden und/oder in Hüllsubstanzen eingebettet sein.Enzymes are those from the class of proteases, lipases, amylases or their mixtures in question. Their proportion can be 0.2 to 1 wt .-%. The enzymes can be adsorbed to carrier substances and / or in coating substances be embedded.
Um Spuren von Schwermetallen zu binden, können die Salze von Polyphosphorsäuren, wie 1-Hydroxyethan-1,1-diphosphonsäure (HEDP) und Diethylentriaminpentamethylenphosphonsäure (DTPMP), bevorzugt in Gewichtsmengen von 0,1 bis 1,0 wt% eingesetzt werden.To bind traces of heavy metals, the salts of Polyphosphoric acids, such as 1-hydroxyethane-1,1-diphosphonic acid (HEDP) and Diethylenetriaminepentamethylenephosphonic acid (DTPMP), preferably in Weight amounts of 0.1 to 1.0 wt% are used.
Als Konservierungsmittel eignen sich beispielsweise Phenoxyethanol, Formaldehydlösung, Parabene, Pentandiol oder Sorbinsäure.Suitable preservatives are, for example, phenoxyethanol, Formaldehyde solution, parabens, pentanediol or sorbic acid.
Als Perlglanzmittel kommen beispielsweise Glycoldistearinsäureester wie Ethylenglycoldistearat, aber auch Fettsäuremonoglycolester in Betracht.As pearlescing agents, for example, glycol distearic acid esters such as Ethylene glycol distearate, but also fatty acid monoglycol esters.
Als Salze bzw. Stellmittel kommen beispielsweise Natriumsulfat, Natriumcarbonat
oder Natriumsilikat (Wasserglas) zum Einsatz.
Als typische Einzelbeispiele für weitere Zusatzstoffe sind Natriumborat, Stärke,
Saccharose, Polydextrose, Stilbenverbindungen, Methylcellulose, Toluolsulfonat,
Cumolsulfonat, Seifen und Silicone zu nennen.As salts or adjusting agents, for example, sodium sulfate, sodium carbonate or sodium silicate (water glass) are used.
Typical individual examples of further additives include sodium borate, starch, sucrose, polydextrose, stilbene compounds, methylcellulose, toluenesulfonate, cumene sulfonate, soaps and silicones.
Die erfindungsgemäßen Mittel sind üblicherweise auf einen pH Wert im Bereich 2 bis 12, bevorzugt pH 2,1 bis 7,8, besonders bevorzugt 2,2 bis 6,5 eingestellt.The agents according to the invention are usually at a pH in the range from 2 to 12, preferably adjusted to pH 2.1 to 7.8, particularly preferably 2.2 to 6.5.
Durch Einsatz von hydrophob modifizierten Acryloyldimethyltaurat enthaltenden Copolymeren gelang es, Formulierungen mit einem pH Wert von < 5 auf Viskositäten oberhalb von 100 mPas zu verdicken. Diese Formulierungen bringen einerseits den Vorteil, dass die Viskosifizierung ein "Verspritzen" des Reinigungsmittels verhindert und dadurch eine sicherere Verwendung gewährleistet. Zudem sorgt die erhöhte Viskosität für ein langsameres Ablaufen des Reinigers von den Oberflächen und garantiert damit eine längere Einwirkzeit. Durch die breite pH-Toleranz der eingesetzten Polymere ist es erstmals möglich stärkere organische Säuren wie beispielsweise Zitronensäure, Äpfelsäure, alpha-Hydroxycarbonsäuren und Oxalsäure in freier Form zu verwenden. Eine verbesserte Wirksamkeit speziell gegen Kalkbeläge kann damit erzielt werden.By using hydrophobically modified Acryloyldimethyltaurat containing Copolymers were able to formulate formulations with a pH of <5 on viscosities above 100 mPas to thicken. These formulations bring on the one hand the Advantage that the viscosification prevents "spattering" of the cleaning agent and thereby ensures a safer use. In addition, the increased ensures Viscosity for a slower drain of the cleaner from the surfaces and thus guarantees a longer exposure time. Due to the wide pH tolerance of the For the first time it is possible to use stronger organic acids such as For example, citric acid, malic acid, alpha-hydroxycarboxylic acids and To use oxalic acid in free form. An improved effectiveness specifically against limescale can be achieved with it.
In den besagten Formulierungen werden hydrophob modifizierte Acryloyldimethyltaurat enthaltenden Copolymere in einer Menge von 0,01 bis 10 Gew.-% eingesetzt. Bevorzugt wird mit einer Menge von 0,1 bis 5 Gew.-% gearbeitet. Besonders bevorzugt ist der Bereich von 0,2 bis 2 Gew.-%. Je nach eingesetzter Polymermenge kann die Viskosität der resultierenden Gele zwischen 100 und 100.000 mPas liegen.In the said formulations are hydrophobically modified Acryloyldimethyltaurat containing copolymers in an amount of 0.01 to 10 wt .-% used. Preference is given to an amount of from 0.1 to 5% by weight worked. Particularly preferred is the range of 0.2 to 2 wt .-%. Depending on used amount of polymer, the viscosity of the resulting gels between 100 and 100,000 mPas lie.
Flüssige Reinigungsgele enthaltend Wasser/organische Lösungsmittel-Gemische Die Verdickung von organischen Lösungsmitteln, speziell Alkoholen, in Kombination mit anionischen und nichtionischen Tensiden und anderen Formulierungsbestandteilen ist durch den Einsatz von hydrophob modifizierten, Acryloyldimethyltaurat enthaltenden Copolymeren leicht möglich. Einschränkend muss angemerkt werden, dass lediglich wasserkompatible organische Lösungsmittel im Sinne der Erfindung sind. Als nicht limitierende Beispiele können Ethanol, Propanol, Isopropanol, DMSO, NMP, Aceton, Methanol und Butanol genannt werden. Die resultierenden Gele können zwischen 0,1 und 90 Gew.-% organischen Lösungsmittelanteil enthalten. Bevorzugt wird ein Anteil von 5 bis 80 Gew.-%. Besonders bevorzugt sind Gele mit einem Gehalt an organischen Lösungsmitteln von 20 bis 60 Gew.-%. Allgemein werden hydrophob modifizierte Acryloyldimethyltaurat enthaltenden Copolymere in diesen Formulierungen in einer Menge von 0,01 bis 10 Gew.-% eingesetzt. Bevorzugt wird mit einer Menge von 0,1 bis 5 Gew.-% gearbeitet. Besonders bevorzugt ist der Bereich von 0,2 bis 2 Gew.-%. Dabei können die Viskositäten der resultierenden Reinigergele enthaltend organische Lösungsmittel zwischen 100 und 100.000 mPas variieren, je nach eingesetzter Polymermenge.Liquid cleansing gels containing water / organic solvent mixtures The thickening of organic solvents, especially alcohols, in combination with anionic and nonionic surfactants and others Formulation ingredients is modified by the use of hydrophobic, Acryloyldimethyltaurat containing copolymers easily possible. restrictive It must be noted that only water-compatible organic solvents within the meaning of the invention. As non-limiting examples, ethanol, Propanol, isopropanol, DMSO, NMP, acetone, methanol and butanol called become. The resulting gels may contain between 0.1 and 90% by weight of organic Contain solvent. Preference is given to a proportion of 5 to 80 wt .-%. Especially preferred are gels containing organic solvents from 20 to 60% by weight. Generally, hydrophobically modified Acryloyldimethyltaurat containing copolymers in these formulations in one Amount of 0.01 to 10 wt .-% used. Preference is given to an amount of 0.1 worked to 5 wt .-%. Particularly preferred is the range of 0.2 to 2 wt .-%. The viscosities of the resulting detergent gels containing organic solvents vary between 100 and 100,000 mPas, depending on used amount of polymer.
Als Einsatzgebiet können auch hier die Reinigung "fettverkrusteter" harter Oberflächen wie Kacheln, Glas oder Keramik oder Metall genannt werden. Mögliche erfindungsgemäße Einsatzgebiete sind beispielsweise Badreiniger, Glasreiniger, und Bodenreiniger.As a field of application can also be here the cleaning "fat-crusted" hard Surfaces such as tiles, glass or ceramic or metal are called. Possible Fields of use according to the invention are, for example, bathroom cleaners, glass cleaners, and Floor cleaner.
Desinfektionsgele spielen im Hygienebereich eine große Rolle und erfreuen sich am Markt seit einigen Jahren steigender Beleibtheit. Speziell Gele in der Verwendung als "flüssige Toilettensteine" sind im sanitären Bereich seit Jahren auf dem Vormarsch.Disinfection gels play a major role in the hygiene sector and enjoy the Market for some years rising obesity. Specially gels in use as "liquid toilet blocks" are in the sanitary area for years on the Rise.
Die Verdickung von wässrigen Desinfektionslösungen durch herkömmliche Verdicker auf Basis von Celluloseethern oder Polyacrylsäuren erfordert teilweise eine hohe Einsatzkonzentration dieser Polymere und ist zudem auf den neutralen bis schwach sauren pH-Bereich beschränkt. The thickening of aqueous disinfectant solutions by conventional thickeners based on cellulose ethers or polyacrylic acids sometimes requires a high Use concentration of these polymers and is also on the neutral to weak acidic pH range limited.
Durch Einsatz von hydrophob modifizierten Acryloyldimethyltaurat enthaltenden Copolymere kann diese Limitierung beseitigt werden. Es ist erstmals möglich, flüssige Desinfektionsmittel enthaltende Reinigungsgele mit sauren Formulierungsbestandteilen wie Fruchtsäure oder alpha-Hydroxycarbonsäuren zu kombinieren und damit neben der antiseptischen auch noch eine "kalklösende" Wirkung zu erzielen.By using hydrophobically modified Acryloyldimethyltaurat containing Copolymers can be overcome this limitation. It is possible for the first time liquid cleansing gels containing acidic disinfectants Formulation ingredients such as fruit acid or alpha-hydroxycarboxylic acids combine and thus in addition to the antiseptic also a "lime-dissolving" Effect.
In den besagten Formulierungen werden hydrophob modifizierten,
Acryloyldimethyltaurat enthaltenden Copolymeren in einer Menge von 0,01 bis
10 Gew.-% eingesetzt. Bevorzugt wird mit einer Menge von 0,1 bis 5 Gew.-%
gearbeitet. Besonders bevorzugt ist der Bereich von 0,2 bis 2 Gew.-%. Je nach
eingesetzter Polymermenge kann die Viskosität der resultierenden Gele zwischen
100 und 100.000 mPas liegen.
Verdickung saurer Peroxid enthaltender Lösungen mit hydrophob modifizierten
AcryloyldimethyltauratpolymerenIn the said formulations, hydrophobically modified copolymers containing acryloyldimethyltaurate are used in an amount of from 0.01 to 10% by weight. Preference is given to working with an amount of 0.1 to 5 wt .-%. Particularly preferred is the range of 0.2 to 2 wt .-%. Depending on the amount of polymer used, the viscosity of the resulting gels can be between 100 and 100,000 mPas.
Thickening of acid peroxide-containing solutions with hydrophobically modified acryloyldimethyltaurate polymers
Für flüssige Formulierungen von Peroxidlösungen ist es wünschenswert diese zu
verdicken. Dadurch wird die Handhabung vereinfacht und sicherer gestaltet.
Erfindungsgemäße Formulierungen können organische oder anorganische Peroxide,
insbesondere Wasserstoffperoxid oder eine Mischung dieser enthalten. Bei
verschiedenen Anwendungen ist es wünschenswert, dass die Peroxidlösungen auf
dem Untergrund haften und nicht Ablaufen, damit die Wirkung zur vollen Entfaltung
kommen kann. Jedoch lassen sich Lösungen von Peroxid mit herkömmlichen
Verdickern nur schwer über einen längeren Zeitraum verdicken bzw. stabilisieren.
Der Grund ist darin zu suchen, dass eine Wasserstoffperoxidlösung bei neutralen
bzw. nur schwach sauren pH-Werten bereits vergleichsweise instabil ist. Bei dem
Zerfall werden auch die Verdicker angegriffen und die Viskosität baut über die Zeit
stark ab. Dadurch kommt es zusätzlich zu einem erheblichen Verlust der
Wasserstoffperoxidaktivität Bei sauren pH-Werten ist der Zerfall von
Wasserstoffperoxid stark retardiert, jedoch bricht die Verdickungsleistung von
Verdickern auf Acrylsäurebasis bei pH-Werten < 5,5 zusammen.
Der Einsatz von erfindungsgemäßen, hydrophob modifizierten
Acryloyldimethyltauratpolymeren in Bleichlösungen verdickt die Formulierung auch
bei pH-Werten deutlich unterhalb des Schwellenwertes von pH 5. Die
Verdickungsleistung der erfindungsgemäßen Polymere bleibt in einem pH-Wert-Intervall
von 1,5 bis 9 nahezu konstant. Es sind mit den erfindungsgemäßen
Verdickern daher sogar Formulierungen mit pH-Werten um pH 2 zugänglich. In
diesem pH-Bereich findet über normale Lagerzeiträume kein merklicher Zerfall von
H2O2 statt, was zu Folge hat, dass die erfindungsgemäßen hydrophob modifizierten
Acryloyldimethyltauratpolymere nicht angegriffen und zerstört werden und somit die
Viskosität der erfindungsgemäßen Formulierung nahezu konstant bleibt.
Im folgenden werden zur Illustration der Erfindung einige nicht beschränkende
Einsatzmöglichkeiten von solchen sauren verdickten Wasserstoffperoxidlösungen
dargestellt:For liquid formulations of peroxide solutions, it is desirable to thicken them. This simplifies handling and makes it safer. Formulations according to the invention may contain organic or inorganic peroxides, in particular hydrogen peroxide or a mixture thereof. In various applications, it is desirable that the peroxide solutions adhere to the substrate rather than draining so that the effect can be fully deployed. However, solutions of peroxide with conventional thickeners are difficult to thicken or stabilize over an extended period of time. The reason lies in the fact that a hydrogen peroxide solution is already comparatively unstable at neutral or only slightly acidic pH values. In the decay, the thickeners are attacked and the viscosity decreases over time greatly. In addition, there is a significant loss of hydrogen peroxide activity. At acidic pH levels, the decomposition of hydrogen peroxide is greatly retarded, but the thickening performance of acrylic acid thickeners breaks down at pH values <5.5.
The use of hydrophobically modified acryloyldimethyltaurate polymers according to the invention in bleaching solutions thickens the formulation even at pH values well below the threshold value of pH 5. The thickening performance of the polymers according to the invention remains virtually constant at a pH value interval of 1.5 to 9. Therefore, with the thickeners according to the invention, even formulations with pH values around pH 2 are accessible. In this pH range, no appreciable decomposition of H2O2 takes place over normal storage periods, with the result that the hydrophobically modified acryloyldimethyltaurate polymers according to the invention are not attacked and destroyed and thus the viscosity of the formulation according to the invention remains virtually constant.
In the following, to illustrate the invention, some non-limiting applications of such acidic thickened hydrogen peroxide solutions are shown:
Bleichlösungen z.B. für die Reinigung von Wäsche (flüssiges Fleckensalz) oder
Geschirr:
Eine Lösung von 0,1 bis 30 %ww H2O2, bevorzugt von 1 bis 15 %ww, besonders
bevorzugt von 3 bis 10 %ww lässt sich mittels erfindungsgemäßer hydrophob
modifizierten Acryloyldimethyltauratpolymere bei pH-Werten < 5 verdicken. Auch bei
erhöhten Lagertemperaturen wird eine über Monate stabile Viskosität gefunden.
Durch die Verdickung der Bleichlösung wird es dem Anwender erleichtert, die
optimale Dosierung einzustellen. Die Lösung verspritzt nicht und die Handhabung
wird dadurch sicherer.Bleaching solutions eg for cleaning laundry (liquid stain salt) or dishes:
A solution of 0.1 to 30% ww H 2 O 2 , preferably from 1 to 15% ww, particularly preferably from 3 to 10% ww can be thickened by means of inventive hydrophobically modified acryloyldimethyltaurate polymers at pH values <5. Even at elevated storage temperatures, a stable viscosity over months is found. The thickening of the bleaching solution makes it easier for the user to set the optimal dosage. The solution does not splash and the handling is safer.
Peroxidhaltige Reiniger können z. B. im Bereich der Reinigung harter Oberflächen im Hygiene- oder Sanitärbereich eingesetzt werden. In diesem Fall können Formulierungen hergestellt werden, die auch anionische und nichtionische Tenside enthalten. Sehr nützlich sind solche Mittel, beispielsweise für die Reinigung von Toiletten. Der peroxidhaltige Reiniger haftet an der Keramik und kann so seine reinigende und desinfizierende Wirkung optimal entfalten.Peroxide-containing cleaners can, for. B. in the field of cleaning hard surfaces in Hygiene or sanitary area are used. In this case, you can Formulations are also prepared which include anionic and nonionic surfactants contain. Very useful are such agents, for example for the cleaning of Toilets. The peroxide-based cleaner adheres to the ceramic and can so his optimally develop cleansing and disinfecting effects.
Gel bzw. Flüssigkeit gefüllte Dauerreiniger (Flüssigtoilettensteine) zum Einhängen in den Spülkasten oder das WC-Becken können mit einer ähnlichen Formulierung realisiert werden. Ein Teil der gelartig verdickten Lösung wird bei jedem Spülvorgang mit dem Wasserstrom im Becken verteilt und sorgt so für eine reinigende und desinfizierende Wirkung. Mit den erfindungsgemäßen hydrophob modifizierten Acryloyldimethytaurat Polymeren sind klare Formulierungen zugänglich, die dem heutigen Trend nach klaren Formulierungen und transparenten Verpackungen entsprechen.Gel or liquid filled permanent cleaners (liquid toilet stones) for hanging in The cistern or the toilet bowl can with a similar formulation will be realized. Part of the gel-like thickened solution becomes with each flushing process distributed with the water flow in the basin, thus ensuring a cleansing and disinfecting effect. With the hydrophobically modified according to the invention Acryloyldimethyltaurate polymers are accessible to clear formulations suitable for the Today's trend for clear formulations and transparent packaging correspond.
Die nachfolgenden Beispiele und Anwendungen sollen die Erfindung näher erläutern, ohne sie jedoch darauf zu beschränken (bei allen Prozentangaben handelt es sich um Gew.-%).The following examples and applications are intended to illustrate the invention in more detail but without restricting it (for all percentages it is wt .-%).
Polymer A ist Poly[acryloyldimethyltaurinsäureammoniumsalz-co-Genapol-T-250-methacrylat-co-Trimethylolpropantrimethacrylat], Mw 570.000 g/mol.Polymer A is poly [acryloyldimethyltauric acid ammonium salt-co-Genapol T-250 methacrylate-co-trimethylolpropane trimethacrylate], Mw 570,000 g / mol.
Polymer B ist Poly[acryloyldimethyltaurinsäurenatriumsalz-co-Genapol-070-acrylat], Mw 1.000.000 g/mol.Polymer B is poly [acryloyldimethyltaurate sodium salt co-Genapol 070 acrylate], Mw 1,000,000 g / mol.
Polymer C ist Poly[acryloyldimethyltaurinsäureammoniumsalz-co-Vinylformamid-co-MPEG 750-methacrylat-co-Trimethylolpropantriacrylat], Mw 1.500.000 g/mol.Polymer C is poly [acryloyldimethyltauric acid ammonium salt-co-vinylformamide-co-MPEG 750-methacrylate-co-trimethylolpropane triacrylate], Mw 1,500,000 g / mol.
Alle Formulierungen enthalten zusätzlich, je nach Bedarf, Konservierungsmittel, Farbstoff und/oder Parfüm.All formulations also contain, as needed, Preservative, dye and / or perfume.
Typische Viskositäten von hochkonzentrierten Formulierungen liegen im Bereich von 700 - 1000 mPas, typische Viskositäten von Gelen liegen im Bereich von 2000 - 3000 mPas.Typical viscosities of highly concentrated formulations are in the range of 700 - 1000 mPas, typical viscosities of gels are in the range of 2000 - 3000 mPas.
Liquid Bleach Booster werden zusätzlich zum Waschmittel in die Waschmaschine dosiert, um die Fleckentfernung zu verbessern. Sie können auch zur Vorbehandlung direkt auf das Gewebe auf den Fleck aufgetragen werden. Die höhere Viskosität täuscht eine höhere Aktivität vor. Bei Direktauftrag kann auch ein gezielteres Aufbringen ermöglicht werden.Liquid Bleach Booster are added to the detergent in the Washer dosed to improve stain removal. she can also be used for pre-treatment directly on the fabric on the stain be applied. The higher viscosity belies a higher one Activity before. For direct order can also be a more targeted application be enabled.
Diese Formulierung müsste noch weiter verdickt werden. Vorteil wäre Vortäuschung einer höheren Aktivität und längere Einwirkzeit/langsamere Ablaufzeit an senkrechten Oberflächen. This formulation would need to be further thickened. Advantage would be Pretense of higher activity and longer exposure time / slower Expiry time on vertical surfaces.
Als Einsatzgebiete für Flüssig-Reinigergele mit pH-Werten < 5 können beispielhaft die Fußboden― und die Kachelreinigung, die Wannen- und Armaturenreinigung und die Toilettenreinigung aufgezählt werden.As applications for liquid cleaning gels with pH values <5 can be exemplified the floor and tile cleaning, the tub and faucet cleaning and the toilet cleaning will be listed.
Claims (7)
R1 eine polymerisationsfähige Funktion aus der Gruppe der vinylisch ungesättigten Verbindungen ist, die zum Aufbau polymerer Strukturen auf radikalischem Wege geeignet ist,
R2 ein linearer oder verzweigter aliphatischer, olefinischer, cycloaliphatischer, arylaliphatischer oder aromatischer (C1-C50)-Kohlenwasserstoffrest, OH, -NH2, -N(CH3)2 oder gleich der Struktureinheit [-Y-R1] ist,
Y für -O-, -C(O)-,-C(O)-O-, -S-, -O-CH2-CH(O-)-CH2OH, -O-CH2-CH(OH)-CH2O-, -O-SO2-O-, -O-SO-O-, -PH-, -P(CH3)-, -PO3-, -NH- und -N(CH3)- steht,
A,B,C und D von Acrylamid, Methacrylamid, Ethylenoxid, Propylenoxid, AMPS, Acrylsäure, Methacrylsäure, Methylmethacrylat, Acrylnitril, Maleinsäure, Vinylacetat, Styrol, 1,3-Butadien, Isopren, Isobuten, Diethylacrylamid und Diisopropylacrylamid abgeleitet sind,
v, w, x und z unabhängig voneinander 0 bis 500 betragen, wobei die Summe der vier Koeffizienten im Mittel ≥1 sein muss.Liquid washing, cleaning, disinfecting and bleaching agents according to one or more of claims 1 to 4, wherein as macromonomers b) compounds according to formula (I) are used
R 1 is a polymerizable function from the group of vinylically unsaturated compounds, which is suitable for the construction of polymeric structures by free radicals,
R 2 is a linear or branched aliphatic, olefinic, cycloaliphatic, arylaliphatic or aromatic (C 1 -C 50 ) -hydrocarbon radical, OH, -NH 2 , -N (CH 3 ) 2 or the structural unit [-YR 1 ],
Y is -O-, -C (O) -, - C (O) -O-, -S-, -O-CH 2 -CH (O -) - CH 2 OH, -O-CH 2 -CH ( OH) -CH 2 O-, -O-SO 2 -O-, -O-SO-O-, -PH-, -P (CH 3 ) -, -PO 3 -, -NH- and -N (CH 3 ) - stands,
A, B, C and D are derived from acrylamide, methacrylamide, ethylene oxide, propylene oxide, AMPS, acrylic acid, methacrylic acid, methyl methacrylate, acrylonitrile, maleic acid, vinyl acetate, styrene, 1,3-butadiene, isoprene, isobutene, diethylacrylamide and diisopropylacrylamide,
v, w, x and z are independently 0 to 500, where the sum of the four coefficients must be on average ≥1.
Applications Claiming Priority (2)
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DE10243661 | 2002-09-19 | ||
DE10243661A DE10243661A1 (en) | 2002-09-19 | 2002-09-19 | Liquid washing and cleaning agents with consistency-giving polymers |
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EP1400583A1 true EP1400583A1 (en) | 2004-03-24 |
EP1400583B1 EP1400583B1 (en) | 2007-01-03 |
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US (1) | US20040058847A1 (en) |
EP (1) | EP1400583B1 (en) |
JP (1) | JP2004107668A (en) |
DE (2) | DE10243661A1 (en) |
ES (1) | ES2280658T3 (en) |
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WO2008095561A3 (en) * | 2007-02-06 | 2008-10-09 | Henkel Ag & Co Kgaa | Detergents |
US8303721B2 (en) | 2007-02-06 | 2012-11-06 | Henkel Ag & Co. Kgaa | Detergent comprising a builder, a bleaching agent, and a copolymer |
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DE102004056554A1 (en) * | 2004-11-23 | 2006-05-24 | Buck-Chemie Gmbh | Adhesive sanitary cleaning and scenting agent |
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EP2211831A1 (en) * | 2007-10-25 | 2010-08-04 | L'Oréal | Fragrancing composition comprising an amphiphilic copolymer of 2 acrylamidomethylpropanesulphonic acid and optionally a cellulose alkyl ether and/or an alkylcellulose alkyl ether |
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EP2771448B1 (en) * | 2011-10-18 | 2015-12-30 | Unilever N.V. | Cleansing composition |
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WO2002044225A2 (en) * | 2000-12-01 | 2002-06-06 | Clariant Gmbh | Silicon-modified comb polymers based on acryloyldimethyl taurine acid (2-acrylamido-2-methyl-1-propanesulfonic acid) |
WO2002044230A2 (en) * | 2000-12-01 | 2002-06-06 | Clariant Gmbh | Compositions containing copolymers based on acryloyldimethyl aminoethylsulfonic acid and synergistic additives |
WO2002043689A2 (en) * | 2000-12-01 | 2002-06-06 | Clariant Gmbh | Cosmetic, pharmaceutical and dermatological products |
Cited By (9)
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WO2006032371A1 (en) * | 2004-09-17 | 2006-03-30 | Henkel Kommanditgesellschaft Auf Aktien | Cleaning agent components |
WO2007022235A1 (en) * | 2005-08-17 | 2007-02-22 | Colgate-Palmolive Company | Acidic cleaning composition containing a hydrophilizing polymer |
US7591272B2 (en) | 2005-08-17 | 2009-09-22 | Colgate-Palmolive Co. | Acidic cleaning composition containing a hydrophilizing polymer, a surfactant, and an acid |
US7635672B1 (en) | 2005-08-17 | 2009-12-22 | Colgate-Palmolive Company | Acidic cleaning composition containing a hydrophilizing polymer, a surfactant, an acid, and a solvent |
WO2008095561A3 (en) * | 2007-02-06 | 2008-10-09 | Henkel Ag & Co Kgaa | Detergents |
US7879154B2 (en) | 2007-02-06 | 2011-02-01 | Henkel Ag & Co. Kgaa | Phosphate-free dishwashing detergents comprising builder, bleaching agent, nonionic surfactant, copolymer and a phosphonate |
US8303721B2 (en) | 2007-02-06 | 2012-11-06 | Henkel Ag & Co. Kgaa | Detergent comprising a builder, a bleaching agent, and a copolymer |
US9752100B2 (en) | 2007-02-06 | 2017-09-05 | Henkel Ag & Co. Kgaa | Detergents |
EP3567094A1 (en) * | 2007-02-06 | 2019-11-13 | Henkel AG & Co. KGaA | Cleaning product |
Also Published As
Publication number | Publication date |
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JP2004107668A (en) | 2004-04-08 |
EP1400583B1 (en) | 2007-01-03 |
US20040058847A1 (en) | 2004-03-25 |
DE50306166D1 (en) | 2007-02-15 |
DE10243661A1 (en) | 2004-04-01 |
ES2280658T3 (en) | 2007-09-16 |
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