CA2297223A1 - Bleaching and disinfecting compositions - Google Patents
Bleaching and disinfecting compositions Download PDFInfo
- Publication number
- CA2297223A1 CA2297223A1 CA 2297223 CA2297223A CA2297223A1 CA 2297223 A1 CA2297223 A1 CA 2297223A1 CA 2297223 CA2297223 CA 2297223 CA 2297223 A CA2297223 A CA 2297223A CA 2297223 A1 CA2297223 A1 CA 2297223A1
- Authority
- CA
- Canada
- Prior art keywords
- composition
- weight
- alkali metal
- percent
- carbon atoms
- 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.)
- Abandoned
Links
- 239000000203 mixture Substances 0.000 title claims abstract description 69
- 238000004061 bleaching Methods 0.000 title claims abstract description 14
- 230000000249 desinfective effect Effects 0.000 title claims abstract description 10
- -1 alkali metal hypochlorites Chemical class 0.000 claims abstract description 34
- 229910052783 alkali metal Inorganic materials 0.000 claims abstract description 14
- WQYVRQLZKVEZGA-UHFFFAOYSA-N hypochlorite Chemical compound Cl[O-] WQYVRQLZKVEZGA-UHFFFAOYSA-N 0.000 claims abstract description 13
- 150000008044 alkali metal hydroxides Chemical class 0.000 claims abstract description 8
- HEMHJVSKTPXQMS-UHFFFAOYSA-M Sodium hydroxide Chemical compound [OH-].[Na+] HEMHJVSKTPXQMS-UHFFFAOYSA-M 0.000 claims description 12
- 125000004432 carbon atom Chemical group C* 0.000 claims description 8
- 235000014113 dietary fatty acids Nutrition 0.000 claims description 8
- 239000000194 fatty acid Substances 0.000 claims description 8
- 229930195729 fatty acid Natural products 0.000 claims description 8
- 150000003839 salts Chemical class 0.000 claims description 8
- 150000001412 amines Chemical class 0.000 claims description 7
- 125000000217 alkyl group Chemical group 0.000 claims description 6
- 239000006260 foam Substances 0.000 claims description 6
- 239000003792 electrolyte Substances 0.000 claims description 5
- DGAQECJNVWCQMB-PUAWFVPOSA-M Ilexoside XXIX Chemical group C[C@@H]1CC[C@@]2(CC[C@@]3(C(=CC[C@H]4[C@]3(CC[C@@H]5[C@@]4(CC[C@@H](C5(C)C)OS(=O)(=O)[O-])C)C)[C@@H]2[C@]1(C)O)C)C(=O)O[C@H]6[C@@H]([C@H]([C@@H]([C@H](O6)CO)O)O)O.[Na+] DGAQECJNVWCQMB-PUAWFVPOSA-M 0.000 claims description 4
- 125000002252 acyl group Chemical group 0.000 claims description 4
- ZLMJMSJWJFRBEC-UHFFFAOYSA-N Potassium Chemical group [K] ZLMJMSJWJFRBEC-UHFFFAOYSA-N 0.000 claims description 3
- 239000005708 Sodium hypochlorite Substances 0.000 claims description 3
- 150000001340 alkali metals Chemical group 0.000 claims description 3
- 150000003009 phosphonic acids Chemical class 0.000 claims description 3
- 229920000058 polyacrylate Polymers 0.000 claims description 3
- 229910052700 potassium Chemical group 0.000 claims description 3
- 239000011591 potassium Chemical group 0.000 claims description 3
- 239000003352 sequestering agent Substances 0.000 claims description 3
- 239000011734 sodium Substances 0.000 claims description 3
- 229910052708 sodium Inorganic materials 0.000 claims description 3
- SUKJFIGYRHOWBL-UHFFFAOYSA-N sodium hypochlorite Chemical compound [Na+].Cl[O-] SUKJFIGYRHOWBL-UHFFFAOYSA-N 0.000 claims description 3
- 229920001732 Lignosulfonate Polymers 0.000 claims description 2
- 229910019142 PO4 Inorganic materials 0.000 claims description 2
- ABLZXFCXXLZCGV-UHFFFAOYSA-N Phosphorous acid Chemical class OP(O)=O ABLZXFCXXLZCGV-UHFFFAOYSA-N 0.000 claims description 2
- 229910052784 alkaline earth metal Inorganic materials 0.000 claims description 2
- 150000001805 chlorine compounds Chemical class 0.000 claims description 2
- 235000021317 phosphate Nutrition 0.000 claims description 2
- 150000003013 phosphoric acid derivatives Chemical class 0.000 claims description 2
- 150000004760 silicates Chemical class 0.000 claims description 2
- 229910000288 alkali metal carbonate Inorganic materials 0.000 claims 1
- 150000008041 alkali metal carbonates Chemical class 0.000 claims 1
- 238000005187 foaming Methods 0.000 abstract description 4
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 abstract description 4
- 239000000654 additive Substances 0.000 abstract description 3
- 238000002360 preparation method Methods 0.000 abstract 1
- KWYUFKZDYYNOTN-UHFFFAOYSA-M Potassium hydroxide Chemical compound [OH-].[K+] KWYUFKZDYYNOTN-UHFFFAOYSA-M 0.000 description 6
- 238000009472 formulation Methods 0.000 description 5
- FPCCDPXRNNVUOM-UHFFFAOYSA-N Hydroxycitronellol Chemical compound OCCC(C)CCCC(C)(C)O FPCCDPXRNNVUOM-UHFFFAOYSA-N 0.000 description 4
- 239000002253 acid Substances 0.000 description 4
- QMVPMAAFGQKVCJ-UHFFFAOYSA-N citronellol Chemical compound OCCC(C)CCC=C(C)C QMVPMAAFGQKVCJ-UHFFFAOYSA-N 0.000 description 4
- RTZKZFJDLAIYFH-UHFFFAOYSA-N ether Substances CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 description 4
- 230000003287 optical effect Effects 0.000 description 4
- YGUMVDWOQQJBGA-VAWYXSNFSA-N 5-[(4-anilino-6-morpholin-4-yl-1,3,5-triazin-2-yl)amino]-2-[(e)-2-[4-[(4-anilino-6-morpholin-4-yl-1,3,5-triazin-2-yl)amino]-2-sulfophenyl]ethenyl]benzenesulfonic acid Chemical compound C=1C=C(\C=C\C=2C(=CC(NC=3N=C(N=C(NC=4C=CC=CC=4)N=3)N3CCOCC3)=CC=2)S(O)(=O)=O)C(S(=O)(=O)O)=CC=1NC(N=C(N=1)N2CCOCC2)=NC=1NC1=CC=CC=C1 YGUMVDWOQQJBGA-VAWYXSNFSA-N 0.000 description 3
- 150000004665 fatty acids Chemical group 0.000 description 3
- 239000002304 perfume Substances 0.000 description 3
- 239000000047 product Substances 0.000 description 3
- 239000004094 surface-active agent Substances 0.000 description 3
- XDOFQFKRPWOURC-UHFFFAOYSA-N 16-methylheptadecanoic acid Chemical compound CC(C)CCCCCCCCCCCCCCC(O)=O XDOFQFKRPWOURC-UHFFFAOYSA-N 0.000 description 2
- WRFXXJKURVTLSY-UHFFFAOYSA-N 2,6-dimethyloctan-2-ol Chemical compound CCC(C)CCCC(C)(C)O WRFXXJKURVTLSY-UHFFFAOYSA-N 0.000 description 2
- DNRJTBAOUJJKDY-UHFFFAOYSA-N 2-Acetyl-3,5,5,6,8,8-hexamethyl-5,6,7,8- tetrahydronaphthalene Chemical compound CC(=O)C1=C(C)C=C2C(C)(C)C(C)CC(C)(C)C2=C1 DNRJTBAOUJJKDY-UHFFFAOYSA-N 0.000 description 2
- LQJBNNIYVWPHFW-UHFFFAOYSA-N 20:1omega9c fatty acid Natural products CCCCCCCCCCC=CCCCCCCCC(O)=O LQJBNNIYVWPHFW-UHFFFAOYSA-N 0.000 description 2
- IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 description 2
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 2
- MHAJPDPJQMAIIY-UHFFFAOYSA-N Hydrogen peroxide Chemical compound OO MHAJPDPJQMAIIY-UHFFFAOYSA-N 0.000 description 2
- ZQPPMHVWECSIRJ-UHFFFAOYSA-N Oleic acid Natural products CCCCCCCCC=CCCCCCCCC(O)=O ZQPPMHVWECSIRJ-UHFFFAOYSA-N 0.000 description 2
- MOYAFQVGZZPNRA-UHFFFAOYSA-N Terpinolene Chemical compound CC(C)=C1CCC(C)=CC1 MOYAFQVGZZPNRA-UHFFFAOYSA-N 0.000 description 2
- 150000004703 alkoxides Chemical class 0.000 description 2
- 150000008051 alkyl sulfates Chemical class 0.000 description 2
- 239000004305 biphenyl Substances 0.000 description 2
- 235000000484 citronellol Nutrition 0.000 description 2
- 238000004140 cleaning Methods 0.000 description 2
- UKMSUNONTOPOIO-UHFFFAOYSA-N docosanoic acid Chemical compound CCCCCCCCCCCCCCCCCCCCCC(O)=O UKMSUNONTOPOIO-UHFFFAOYSA-N 0.000 description 2
- POULHZVOKOAJMA-UHFFFAOYSA-N dodecanoic acid Chemical class CCCCCCCCCCCC(O)=O POULHZVOKOAJMA-UHFFFAOYSA-N 0.000 description 2
- 239000000975 dye Substances 0.000 description 2
- ZQPPMHVWECSIRJ-MDZDMXLPSA-N elaidic acid Chemical compound CCCCCCCC\C=C\CCCCCCCC(O)=O ZQPPMHVWECSIRJ-MDZDMXLPSA-N 0.000 description 2
- HCRBXQFHJMCTLF-ZCFIWIBFSA-N ethyl (2r)-2-methylbutanoate Chemical compound CCOC(=O)[C@H](C)CC HCRBXQFHJMCTLF-ZCFIWIBFSA-N 0.000 description 2
- IPCSVZSSVZVIGE-UHFFFAOYSA-N hexadecanoic acid Chemical compound CCCCCCCCCCCCCCCC(O)=O IPCSVZSSVZVIGE-UHFFFAOYSA-N 0.000 description 2
- QXJSBBXBKPUZAA-UHFFFAOYSA-N isooleic acid Natural products CCCCCCCC=CCCCCCCCCC(O)=O QXJSBBXBKPUZAA-UHFFFAOYSA-N 0.000 description 2
- CDOSHBSSFJOMGT-UHFFFAOYSA-N linalool Chemical compound CC(C)=CCCC(C)(O)C=C CDOSHBSSFJOMGT-UHFFFAOYSA-N 0.000 description 2
- UWKAYLJWKGQEPM-LBPRGKRZSA-N linalyl acetate Chemical compound CC(C)=CCC[C@](C)(C=C)OC(C)=O UWKAYLJWKGQEPM-LBPRGKRZSA-N 0.000 description 2
- UODXCYZDMHPIJE-UHFFFAOYSA-N menthanol Chemical compound CC1CCC(C(C)(C)O)CC1 UODXCYZDMHPIJE-UHFFFAOYSA-N 0.000 description 2
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 description 2
- DUNCVNHORHNONW-UHFFFAOYSA-N myrcenol Chemical compound CC(C)(O)CCCC(=C)C=C DUNCVNHORHNONW-UHFFFAOYSA-N 0.000 description 2
- 239000002736 nonionic surfactant Substances 0.000 description 2
- SECPZKHBENQXJG-FPLPWBNLSA-N palmitoleic acid Chemical compound CCCCCC\C=C/CCCCCCCC(O)=O SECPZKHBENQXJG-FPLPWBNLSA-N 0.000 description 2
- 239000000049 pigment Substances 0.000 description 2
- 229920000151 polyglycol Polymers 0.000 description 2
- 239000010695 polyglycol Substances 0.000 description 2
- BWHMMNNQKKPAPP-UHFFFAOYSA-L potassium carbonate Chemical compound [K+].[K+].[O-]C([O-])=O BWHMMNNQKKPAPP-UHFFFAOYSA-L 0.000 description 2
- CZCBTSFUTPZVKJ-UHFFFAOYSA-N rose oxide Chemical compound CC1CCOC(C=C(C)C)C1 CZCBTSFUTPZVKJ-UHFFFAOYSA-N 0.000 description 2
- 159000000000 sodium salts Chemical class 0.000 description 2
- 239000000126 substance Substances 0.000 description 2
- 239000001490 (3R)-3,7-dimethylocta-1,6-dien-3-ol Substances 0.000 description 1
- CUXYLFPMQMFGPL-WPOADVJFSA-N (9Z,11E,13E)-octadeca-9,11,13-trienoic acid Chemical compound CCCC\C=C\C=C\C=C/CCCCCCCC(O)=O CUXYLFPMQMFGPL-WPOADVJFSA-N 0.000 description 1
- OYHQOLUKZRVURQ-NTGFUMLPSA-N (9Z,12Z)-9,10,12,13-tetratritiooctadeca-9,12-dienoic acid Chemical compound C(CCCCCCC\C(=C(/C\C(=C(/CCCCC)\[3H])\[3H])\[3H])\[3H])(=O)O OYHQOLUKZRVURQ-NTGFUMLPSA-N 0.000 description 1
- WRIDQFICGBMAFQ-UHFFFAOYSA-N (E)-8-Octadecenoic acid Natural products CCCCCCCCCC=CCCCCCCC(O)=O WRIDQFICGBMAFQ-UHFFFAOYSA-N 0.000 description 1
- QMVPMAAFGQKVCJ-SNVBAGLBSA-N (R)-(+)-citronellol Natural products OCC[C@H](C)CCC=C(C)C QMVPMAAFGQKVCJ-SNVBAGLBSA-N 0.000 description 1
- CDOSHBSSFJOMGT-JTQLQIEISA-N (R)-linalool Natural products CC(C)=CCC[C@@](C)(O)C=C CDOSHBSSFJOMGT-JTQLQIEISA-N 0.000 description 1
- KTZQTRPPVKQPFO-UHFFFAOYSA-N 1,2-benzoxazole Chemical compound C1=CC=C2C=NOC2=C1 KTZQTRPPVKQPFO-UHFFFAOYSA-N 0.000 description 1
- BCMCBBGGLRIHSE-UHFFFAOYSA-N 1,3-benzoxazole Chemical compound C1=CC=C2OC=NC2=C1 BCMCBBGGLRIHSE-UHFFFAOYSA-N 0.000 description 1
- ZMLPKJYZRQZLDA-UHFFFAOYSA-N 1-(2-phenylethenyl)-4-[4-(2-phenylethenyl)phenyl]benzene Chemical group C=1C=CC=CC=1C=CC(C=C1)=CC=C1C(C=C1)=CC=C1C=CC1=CC=CC=C1 ZMLPKJYZRQZLDA-UHFFFAOYSA-N 0.000 description 1
- HYZJCKYKOHLVJF-UHFFFAOYSA-N 1H-benzimidazole Chemical compound C1=CC=C2NC=NC2=C1 HYZJCKYKOHLVJF-UHFFFAOYSA-N 0.000 description 1
- MSDBCXHVDKLCCF-UHFFFAOYSA-N 2,6-dimethyloctan-3-ol Chemical compound CCC(C)CCC(O)C(C)C MSDBCXHVDKLCCF-UHFFFAOYSA-N 0.000 description 1
- VIFBEEYZXDDZCT-UHFFFAOYSA-N 2-(2-phenylethenyl)benzenesulfonic acid Chemical compound OS(=O)(=O)C1=CC=CC=C1C=CC1=CC=CC=C1 VIFBEEYZXDDZCT-UHFFFAOYSA-N 0.000 description 1
- PCANHPMMPLOBDQ-UHFFFAOYSA-N 2-[2-[4-[4-[2-(4-chlorophenyl)ethenyl]phenyl]phenyl]ethenyl]benzenesulfonic acid Chemical group OS(=O)(=O)C1=CC=CC=C1C=CC1=CC=C(C=2C=CC(C=CC=3C=CC(Cl)=CC=3)=CC=2)C=C1 PCANHPMMPLOBDQ-UHFFFAOYSA-N 0.000 description 1
- ZILZQZGAJNDJIY-UHFFFAOYSA-N 2-chloro-5-[2-[4-[4-[2-(4-chloro-3-sulfophenyl)ethenyl]phenyl]phenyl]ethenyl]benzenesulfonic acid Chemical group C1=C(Cl)C(S(=O)(=O)O)=CC(C=CC=2C=CC(=CC=2)C=2C=CC(C=CC=3C=C(C(Cl)=CC=3)S(O)(=O)=O)=CC=2)=C1 ZILZQZGAJNDJIY-UHFFFAOYSA-N 0.000 description 1
- YTZPUTADNGREHA-UHFFFAOYSA-N 2h-benzo[e]benzotriazole Chemical compound C1=CC2=CC=CC=C2C2=NNN=C21 YTZPUTADNGREHA-UHFFFAOYSA-N 0.000 description 1
- TZOYXRMEFDYWDQ-UHFFFAOYSA-N 3,4-dihydro-1h-quinolin-2-one Chemical compound C1=CC=C2NC(=O)CCC2=C1 TZOYXRMEFDYWDQ-UHFFFAOYSA-N 0.000 description 1
- LDKNWIFAWPRIJH-UHFFFAOYSA-N 3,7-dimethyloctan-1-ol 2-methylnonan-2-ol Chemical compound CCCCCCCC(C)(C)O.CC(C)CCCC(C)CCO LDKNWIFAWPRIJH-UHFFFAOYSA-N 0.000 description 1
- GOLORTLGFDVFDW-UHFFFAOYSA-N 3-(1h-benzimidazol-2-yl)-7-(diethylamino)chromen-2-one Chemical compound C1=CC=C2NC(C3=CC4=CC=C(C=C4OC3=O)N(CC)CC)=NC2=C1 GOLORTLGFDVFDW-UHFFFAOYSA-N 0.000 description 1
- VAJVDSVGBWFCLW-UHFFFAOYSA-N 3-Phenyl-1-propanol Chemical compound OCCCC1=CC=CC=C1 VAJVDSVGBWFCLW-UHFFFAOYSA-N 0.000 description 1
- SATQWIIUJKWZNO-UHFFFAOYSA-N 5-(3,3-dimethyloxiran-2-yl)-3-methylpent-1-en-3-ol Chemical compound C=CC(O)(C)CCC1OC1(C)C SATQWIIUJKWZNO-UHFFFAOYSA-N 0.000 description 1
- VJUCYHWKAJNBKY-UHFFFAOYSA-N 5-amino-2-[2-(4-amino-2-sulfophenyl)ethenyl]benzenesulfonic acid 4-oxo-2-phenylchromene-3-carboxylic acid Chemical class O1C(=C(C(=O)C2=CC=CC=C12)C(=O)O)C1=CC=CC=C1.NC=1C=C(C(=CC1)C=CC=1C(=CC(=CC1)N)S(=O)(=O)O)S(=O)(=O)O VJUCYHWKAJNBKY-UHFFFAOYSA-N 0.000 description 1
- REJHVSOVQBJEBF-OWOJBTEDSA-N 5-azaniumyl-2-[(e)-2-(4-azaniumyl-2-sulfonatophenyl)ethenyl]benzenesulfonate Chemical class OS(=O)(=O)C1=CC(N)=CC=C1\C=C\C1=CC=C(N)C=C1S(O)(=O)=O REJHVSOVQBJEBF-OWOJBTEDSA-N 0.000 description 1
- WWJLCYHYLZZXBE-UHFFFAOYSA-N 5-chloro-1,3-dihydroindol-2-one Chemical compound ClC1=CC=C2NC(=O)CC2=C1 WWJLCYHYLZZXBE-UHFFFAOYSA-N 0.000 description 1
- QSBYPNXLFMSGKH-UHFFFAOYSA-N 9-Heptadecensaeure Natural products CCCCCCCC=CCCCCCCCC(O)=O QSBYPNXLFMSGKH-UHFFFAOYSA-N 0.000 description 1
- QTBSBXVTEAMEQO-UHFFFAOYSA-M Acetate Chemical compound CC([O-])=O QTBSBXVTEAMEQO-UHFFFAOYSA-M 0.000 description 1
- 235000021357 Behenic acid Nutrition 0.000 description 1
- DPUOLQHDNGRHBS-UHFFFAOYSA-N Brassidinsaeure Natural products CCCCCCCCC=CCCCCCCCCCCCC(O)=O DPUOLQHDNGRHBS-UHFFFAOYSA-N 0.000 description 1
- VEXZGXHMUGYJMC-UHFFFAOYSA-M Chloride anion Chemical compound [Cl-] VEXZGXHMUGYJMC-UHFFFAOYSA-M 0.000 description 1
- ZAMOUSCENKQFHK-UHFFFAOYSA-N Chlorine atom Chemical compound [Cl] ZAMOUSCENKQFHK-UHFFFAOYSA-N 0.000 description 1
- URXZXNYJPAJJOQ-UHFFFAOYSA-N Erucic acid Natural products CCCCCCC=CCCCCCCCCCCCC(O)=O URXZXNYJPAJJOQ-UHFFFAOYSA-N 0.000 description 1
- IAYPIBMASNFSPL-UHFFFAOYSA-N Ethylene oxide Chemical compound C1CO1 IAYPIBMASNFSPL-UHFFFAOYSA-N 0.000 description 1
- PIICEJLVQHRZGT-UHFFFAOYSA-N Ethylenediamine Chemical compound NCCN PIICEJLVQHRZGT-UHFFFAOYSA-N 0.000 description 1
- KGEKLUUHTZCSIP-UHFFFAOYSA-N Isobornyl acetate Natural products C1CC2(C)C(OC(=O)C)CC1C2(C)C KGEKLUUHTZCSIP-UHFFFAOYSA-N 0.000 description 1
- 239000005639 Lauric acid Substances 0.000 description 1
- WHXSMMKQMYFTQS-UHFFFAOYSA-N Lithium Chemical compound [Li] WHXSMMKQMYFTQS-UHFFFAOYSA-N 0.000 description 1
- 239000005642 Oleic acid Substances 0.000 description 1
- 235000021314 Palmitic acid Nutrition 0.000 description 1
- 235000021319 Palmitoleic acid Nutrition 0.000 description 1
- DYUQAZSOFZSPHD-UHFFFAOYSA-N Phenylpropyl alcohol Natural products CCC(O)C1=CC=CC=C1 DYUQAZSOFZSPHD-UHFFFAOYSA-N 0.000 description 1
- GOOHAUXETOMSMM-UHFFFAOYSA-N Propylene oxide Chemical compound CC1CO1 GOOHAUXETOMSMM-UHFFFAOYSA-N 0.000 description 1
- 229910006127 SO3X Inorganic materials 0.000 description 1
- 235000021355 Stearic acid Nutrition 0.000 description 1
- ULUAUXLGCMPNKK-UHFFFAOYSA-N Sulfobutanedioic acid Chemical class OC(=O)CC(C(O)=O)S(O)(=O)=O ULUAUXLGCMPNKK-UHFFFAOYSA-N 0.000 description 1
- 239000001940 [(1R,4S,6R)-1,7,7-trimethyl-6-bicyclo[2.2.1]heptanyl] acetate Substances 0.000 description 1
- 150000001298 alcohols Chemical class 0.000 description 1
- 150000001339 alkali metal compounds Chemical class 0.000 description 1
- 229940045714 alkyl sulfonate alkylating agent Drugs 0.000 description 1
- 150000008052 alkyl sulfonates Chemical class 0.000 description 1
- DTOSIQBPPRVQHS-PDBXOOCHSA-N alpha-linolenic acid Chemical compound CC\C=C/C\C=C/C\C=C/CCCCCCCC(O)=O DTOSIQBPPRVQHS-PDBXOOCHSA-N 0.000 description 1
- 235000020661 alpha-linolenic acid Nutrition 0.000 description 1
- 125000002490 anilino group Chemical group [H]N(*)C1=C([H])C([H])=C([H])C([H])=C1[H] 0.000 description 1
- 125000000129 anionic group Chemical group 0.000 description 1
- 239000003945 anionic surfactant Substances 0.000 description 1
- 229940116226 behenic acid Drugs 0.000 description 1
- JGQFVRIQXUFPAH-UHFFFAOYSA-N beta-citronellol Natural products OCCC(C)CCCC(C)=C JGQFVRIQXUFPAH-UHFFFAOYSA-N 0.000 description 1
- 235000010290 biphenyl Nutrition 0.000 description 1
- 239000001045 blue dye Substances 0.000 description 1
- 239000003093 cationic surfactant Substances 0.000 description 1
- 239000000460 chlorine Substances 0.000 description 1
- 229910052801 chlorine Inorganic materials 0.000 description 1
- SECPZKHBENQXJG-UHFFFAOYSA-N cis-palmitoleic acid Natural products CCCCCCC=CCCCCCCCC(O)=O SECPZKHBENQXJG-UHFFFAOYSA-N 0.000 description 1
- 150000001875 compounds Chemical class 0.000 description 1
- 239000007859 condensation product Substances 0.000 description 1
- PMPJQLCPEQFEJW-UHFFFAOYSA-L disodium;2-[2-[4-[4-[2-(2-sulfonatophenyl)ethenyl]phenyl]phenyl]ethenyl]benzenesulfonate Chemical compound [Na+].[Na+].[O-]S(=O)(=O)C1=CC=CC=C1C=CC1=CC=C(C=2C=CC(C=CC=3C(=CC=CC=3)S([O-])(=O)=O)=CC=2)C=C1 PMPJQLCPEQFEJW-UHFFFAOYSA-L 0.000 description 1
- 230000000694 effects Effects 0.000 description 1
- DPUOLQHDNGRHBS-KTKRTIGZSA-N erucic acid Chemical compound CCCCCCCC\C=C/CCCCCCCCCCCC(O)=O DPUOLQHDNGRHBS-KTKRTIGZSA-N 0.000 description 1
- 150000002148 esters Chemical class 0.000 description 1
- 150000002170 ethers Chemical class 0.000 description 1
- 239000001813 ethyl (2R)-2-methylbutanoate Substances 0.000 description 1
- 229940090910 ethyl 2-methylbutyrate Drugs 0.000 description 1
- 239000003925 fat Substances 0.000 description 1
- 235000019197 fats Nutrition 0.000 description 1
- 150000002191 fatty alcohols Chemical class 0.000 description 1
- LQJBNNIYVWPHFW-QXMHVHEDSA-N gadoleic acid Chemical compound CCCCCCCCCC\C=C/CCCCCCCC(O)=O LQJBNNIYVWPHFW-QXMHVHEDSA-N 0.000 description 1
- ONKNPOPIGWHAQC-UHFFFAOYSA-N galaxolide Chemical compound C1OCC(C)C2=C1C=C1C(C)(C)C(C)C(C)(C)C1=C2 ONKNPOPIGWHAQC-UHFFFAOYSA-N 0.000 description 1
- 229910001385 heavy metal Inorganic materials 0.000 description 1
- LIIALPBMIOVAHH-UHFFFAOYSA-N herniarin Chemical compound C1=CC(=O)OC2=CC(OC)=CC=C21 LIIALPBMIOVAHH-UHFFFAOYSA-N 0.000 description 1
- JHGVLAHJJNKSAW-UHFFFAOYSA-N herniarin Natural products C1CC(=O)OC2=CC(OC)=CC=C21 JHGVLAHJJNKSAW-UHFFFAOYSA-N 0.000 description 1
- 230000007062 hydrolysis Effects 0.000 description 1
- 238000006460 hydrolysis reaction Methods 0.000 description 1
- 239000003752 hydrotrope Substances 0.000 description 1
- VKOBVWXKNCXXDE-UHFFFAOYSA-N icosanoic acid Chemical compound CCCCCCCCCCCCCCCCCCCC(O)=O VKOBVWXKNCXXDE-UHFFFAOYSA-N 0.000 description 1
- 238000011065 in-situ storage Methods 0.000 description 1
- 239000004615 ingredient Substances 0.000 description 1
- 150000002500 ions Chemical class 0.000 description 1
- SUMDYPCJJOFFON-UHFFFAOYSA-N isethionic acid Chemical class OCCS(O)(=O)=O SUMDYPCJJOFFON-UHFFFAOYSA-N 0.000 description 1
- 229930007744 linalool Natural products 0.000 description 1
- UWKAYLJWKGQEPM-UHFFFAOYSA-N linalool acetate Natural products CC(C)=CCCC(C)(C=C)OC(C)=O UWKAYLJWKGQEPM-UHFFFAOYSA-N 0.000 description 1
- 229960004488 linolenic acid Drugs 0.000 description 1
- KQQKGWQCNNTQJW-UHFFFAOYSA-N linolenic acid Natural products CC=CCCC=CCC=CCCCCCCCC(O)=O KQQKGWQCNNTQJW-UHFFFAOYSA-N 0.000 description 1
- 239000012263 liquid product Substances 0.000 description 1
- 229910052744 lithium Inorganic materials 0.000 description 1
- 229910021645 metal ion Inorganic materials 0.000 description 1
- 125000000250 methylamino group Chemical group [H]N(*)C([H])([H])[H] 0.000 description 1
- ZLQJVGSVJRBUNL-UHFFFAOYSA-N methylumbelliferone Natural products C1=C(O)C=C2OC(=O)C(C)=CC2=C1 ZLQJVGSVJRBUNL-UHFFFAOYSA-N 0.000 description 1
- 229930008383 myrcenol Natural products 0.000 description 1
- WQEPLUUGTLDZJY-UHFFFAOYSA-N n-Pentadecanoic acid Natural products CCCCCCCCCCCCCCC(O)=O WQEPLUUGTLDZJY-UHFFFAOYSA-N 0.000 description 1
- HRRDCWDFRIJIQZ-UHFFFAOYSA-N naphthalene-1,8-dicarboxylic acid Chemical compound C1=CC(C(O)=O)=C2C(C(=O)O)=CC=CC2=C1 HRRDCWDFRIJIQZ-UHFFFAOYSA-N 0.000 description 1
- 238000006386 neutralization reaction Methods 0.000 description 1
- 229910052757 nitrogen Inorganic materials 0.000 description 1
- QIQXTHQIDYTFRH-UHFFFAOYSA-N octadecanoic acid Chemical compound CCCCCCCCCCCCCCCCCC(O)=O QIQXTHQIDYTFRH-UHFFFAOYSA-N 0.000 description 1
- OQCDKBAXFALNLD-UHFFFAOYSA-N octadecanoic acid Natural products CCCCCCCC(C)CCCCCCCCC(O)=O OQCDKBAXFALNLD-UHFFFAOYSA-N 0.000 description 1
- 239000003921 oil Substances 0.000 description 1
- 230000003647 oxidation Effects 0.000 description 1
- 238000007254 oxidation reaction Methods 0.000 description 1
- CNVZJPUDSLNTQU-SEYXRHQNSA-N petroselinic acid Chemical compound CCCCCCCCCCC\C=C/CCCCC(O)=O CNVZJPUDSLNTQU-SEYXRHQNSA-N 0.000 description 1
- ZUOUZKKEUPVFJK-UHFFFAOYSA-N phenylbenzene Natural products C1=CC=CC=C1C1=CC=CC=C1 ZUOUZKKEUPVFJK-UHFFFAOYSA-N 0.000 description 1
- XAEFZNCEHLXOMS-UHFFFAOYSA-M potassium benzoate Chemical compound [K+].[O-]C(=O)C1=CC=CC=C1 XAEFZNCEHLXOMS-UHFFFAOYSA-M 0.000 description 1
- 229910000027 potassium carbonate Inorganic materials 0.000 description 1
- 235000011164 potassium chloride Nutrition 0.000 description 1
- 159000000001 potassium salts Chemical class 0.000 description 1
- 229930007790 rose oxide Natural products 0.000 description 1
- CDBYLPFSWZWCQE-UHFFFAOYSA-L sodium carbonate Substances [Na+].[Na+].[O-]C([O-])=O CDBYLPFSWZWCQE-UHFFFAOYSA-L 0.000 description 1
- 229910000029 sodium carbonate Inorganic materials 0.000 description 1
- RPACBEVZENYWOL-XFULWGLBSA-M sodium;(2r)-2-[6-(4-chlorophenoxy)hexyl]oxirane-2-carboxylate Chemical compound [Na+].C=1C=C(Cl)C=CC=1OCCCCCC[C@]1(C(=O)[O-])CO1 RPACBEVZENYWOL-XFULWGLBSA-M 0.000 description 1
- 239000008117 stearic acid Substances 0.000 description 1
- 238000004659 sterilization and disinfection Methods 0.000 description 1
- 238000003756 stirring Methods 0.000 description 1
- 230000019635 sulfation Effects 0.000 description 1
- 238000005670 sulfation reaction Methods 0.000 description 1
- 150000003467 sulfuric acid derivatives Chemical class 0.000 description 1
- 239000003760 tallow Substances 0.000 description 1
- TUNFSRHWOTWDNC-HKGQFRNVSA-N tetradecanoic acid Chemical class CCCCCCCCCCCCC[14C](O)=O TUNFSRHWOTWDNC-HKGQFRNVSA-N 0.000 description 1
- 239000004753 textile Substances 0.000 description 1
- 230000008719 thickening Effects 0.000 description 1
- GDJZZWYLFXAGFH-UHFFFAOYSA-M xylenesulfonate group Chemical group C1(C(C=CC=C1)C)(C)S(=O)(=O)[O-] GDJZZWYLFXAGFH-UHFFFAOYSA-M 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C11—ANIMAL OR VEGETABLE OILS, FATS, FATTY SUBSTANCES OR WAXES; FATTY ACIDS THEREFROM; DETERGENTS; CANDLES
- C11D—DETERGENT COMPOSITIONS; USE OF SINGLE SUBSTANCES AS DETERGENTS; SOAP OR SOAP-MAKING; RESIN SOAPS; RECOVERY OF GLYCEROL
- C11D3/00—Other compounding ingredients of detergent compositions covered in group C11D1/00
- C11D3/02—Inorganic compounds ; Elemental compounds
- C11D3/04—Water-soluble compounds
- C11D3/044—Hydroxides or bases
-
- C—CHEMISTRY; METALLURGY
- C11—ANIMAL OR VEGETABLE OILS, FATS, FATTY SUBSTANCES OR WAXES; FATTY ACIDS THEREFROM; DETERGENTS; CANDLES
- C11D—DETERGENT COMPOSITIONS; USE OF SINGLE SUBSTANCES AS DETERGENTS; SOAP OR SOAP-MAKING; RESIN SOAPS; RECOVERY OF GLYCEROL
- C11D1/00—Detergent compositions based essentially on surface-active compounds; Use of these compounds as a detergent
- C11D1/66—Non-ionic compounds
- C11D1/83—Mixtures of non-ionic with anionic compounds
-
- C—CHEMISTRY; METALLURGY
- C11—ANIMAL OR VEGETABLE OILS, FATS, FATTY SUBSTANCES OR WAXES; FATTY ACIDS THEREFROM; DETERGENTS; CANDLES
- C11D—DETERGENT COMPOSITIONS; USE OF SINGLE SUBSTANCES AS DETERGENTS; SOAP OR SOAP-MAKING; RESIN SOAPS; RECOVERY OF GLYCEROL
- C11D3/00—Other compounding ingredients of detergent compositions covered in group C11D1/00
- C11D3/395—Bleaching agents
- C11D3/3956—Liquid compositions
-
- C—CHEMISTRY; METALLURGY
- C11—ANIMAL OR VEGETABLE OILS, FATS, FATTY SUBSTANCES OR WAXES; FATTY ACIDS THEREFROM; DETERGENTS; CANDLES
- C11D—DETERGENT COMPOSITIONS; USE OF SINGLE SUBSTANCES AS DETERGENTS; SOAP OR SOAP-MAKING; RESIN SOAPS; RECOVERY OF GLYCEROL
- C11D1/00—Detergent compositions based essentially on surface-active compounds; Use of these compounds as a detergent
- C11D1/02—Anionic compounds
- C11D1/12—Sulfonic acids or sulfuric acid esters; Salts thereof
- C11D1/29—Sulfates of polyoxyalkylene ethers
-
- C—CHEMISTRY; METALLURGY
- C11—ANIMAL OR VEGETABLE OILS, FATS, FATTY SUBSTANCES OR WAXES; FATTY ACIDS THEREFROM; DETERGENTS; CANDLES
- C11D—DETERGENT COMPOSITIONS; USE OF SINGLE SUBSTANCES AS DETERGENTS; SOAP OR SOAP-MAKING; RESIN SOAPS; RECOVERY OF GLYCEROL
- C11D1/00—Detergent compositions based essentially on surface-active compounds; Use of these compounds as a detergent
- C11D1/66—Non-ionic compounds
- C11D1/75—Amino oxides
Landscapes
- Chemical & Material Sciences (AREA)
- Life Sciences & Earth Sciences (AREA)
- Engineering & Computer Science (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Oil, Petroleum & Natural Gas (AREA)
- Wood Science & Technology (AREA)
- Organic Chemistry (AREA)
- Inorganic Chemistry (AREA)
- Detergent Compositions (AREA)
Abstract
The invention relates to new bleaching and disinfecting compositions containing - based on the composition -(a) 1.0 to 6.0% by weight alkali metal hypochlorites, (b) 0.1 to 5.0% by weight alkyl ether sulfates, (c) 0.5 to 5.0% by weight amidoamine oxides and (d) 0.5 to 2.0% by weight alkali metal hydroxides, with the proviso that the quantities shown add up to 100% by weight with water and, optionally, other auxiliaries and additives. The preparations reduce the viscosity and foaming of hypochlorite solutions.
Description
Bleaching and Disinfecting Compositions Field of the Invention This invention relates to new aqueous bleaching and disinfecting compositions containing alkali metal hypochlorites, alkyl ether sulfates, amidoamine oxides and alkali metal hydroxides in defined quantity ratios.
Background of the Invention In the past, bleaching compositions based on alkali metal hypo-chlorites which have a remarkable viscosity and which are therefore suitable both for the treatment of horizontal surfaces and for the treatment of sloping and, above all, vertical surfaces have been successfully used in the field of hygiene and disinfection and in the textile treatment field. The effect of the high viscosity of these compositions is that the contact time between them and the surfaces to be treated is considerably longer than in the case of commercially available liquid products which soon flow off the surface.
Various publications relating to such viscous bleaching and disinfecting compositions are known from the literature. A few patents on this subject are mentioned by way of example in the following.
EP 0 274 885 A (ICI), for example, recommends the use of mixtures of linear and branched amine oxides. ES 88 01 389 A (Henkel Iberica) relates to bleaching compositions based on aqueous hypochlorite solutions which predominantly contain alkyl ether sulfates and, in addition, small amounts of amine oxides as their surfactant component. In DE 43 33 100 C1, applicants describe stable and sufficiently viscous aqueous bleaching and cleaning compositions based on hypochlorites, fatty alcohol ether sulfates and amine oxides which contain as a compulsory component amine oxide phosphonic acids which make a crucial contribution towards the thickening the compositions.
In practice, the viscosity of the hypochlorite solutions known from the literature is often too high for cleaning hard surfaces (viscosities of 50 mPas and higher, as measured in a Brookfield LV viscosimeter at 20°C, spindle 1, 60 r.p.m.). In addition, the excessive foaming (foam heights of 100 mm and more, as measured by the Ross-Miles test at 20°C) is often regarded as problematical. Compared with the hitherto known products, less expensive bleaching and disinfecting compositions would also be desirable.
Accordingly, the problem addressed by the present invention was to provide new water-containing bleaching and disinfecting compositions which would generate less foam and would be less viscous than the known compositions. Finally, another problem addressed by the invention was to provide compositions which would be distinguished by a price advantage over the hitherto known hypochlorite bleaching compositions.
Description of the Invention The present invention relates to bleaching and disinfecting compositions containing - based on the composition -(a) 1.0 to 6.0% by weight alkali metal hypochlorites, (b) 0.1 to 5.0% by weight alkyl ether sulfates, (c) 0.5 to 5.0% by weight amidoamine oxides and (d) 0.5 to 2.0% by weight alkali metal hydroxides, with the proviso that the quantities shown add up to 100% by weight with water and, optionally, other auxiliaries and additives.
It has surprisingly been found that the addition of amidoamine oxides to bleaching and disinfecting compositions reduces not only their viscosity, but also their foaming. Viscosities below 50 mPas (Brookfield LVT viscosimeter, 20°C, spindle 1, 60 r.p.m.) and foam heights below 100 mm (Ross-Miles test, 20°C) have been measured for the compositions according to the invention. In addition, the amidoamine oxides used in the mixture represent a much more favorably priced alternative to the amine oxides conventionally used.
Alkali metal hypochlorites Alkali metal hypochlorites in the context of the present invention are lithium, potassium and, in particular, sodium hypochlorite. The hypochlo-rites may advantageously be used in quantities of 1.0 to 6.0% by weight and preferably in quantities of 3.0 to 5.0% by weight, based on the composition.
Alkyl ether sulfates Alkyl ether sulfates are known anionic surfactants which may be obtained by sulfation of nonionic surfactants of the alkyl polyglycol ether type and subsequent neutralization. Alkyl ether sulfates suitable for use in the compositions according to the invention correspond to formula (I):
R'O-(CH2CH2O)"SO3X (~) in which R' is an alkyl group containing 12 to 18 carbon atoms, n is a number of 2 to 5 and X represents sodium or potassium. Typical examples are the sodium salts of sulfates of the C~2,~4 cocofatty alcohol 2 EO, 2.3 EO
and 3 EO adduct. The alkyl ether sulfates may have a conventional or narrow homolog distribution. The alkyl ether sulfates are used in quantities of preferably 0.1 to 5.0% by weight and more preferably 0.2 to 1.5% by weight, based on the composition.
Amidoamine oxides Amidoamine oxides are known substances which are occasionally classed as cationic surfactants, but generally as nonionic surfactants.
They are produced from tertiary fatty acid amidoamines of which the anionic nitrogen is oxidized with hydrogen peroxide. The amidoamine oxides suitable for use in accordance with the invention correspond to formula (II):
R2CONH(CH2)", i ->O (II) in which R2C0 is a linear or branched acyl group containing 12 to 18 carbon atoms, R3 and R4 independently of one another represent an optionally hydroxysubstituted alkyl group containing 1 to 4 carbon atoms and m is a number of 1 to 3. Amidoamine oxides corresponding to formula (11), in which R2C0 is a cocoacyl group, R3 and R4 represent a methyl or a hydroxyethyl group and m has a value of 2, are preferably used. The amidoamine oxides are used in quantities of preferably 0.5 to 5.0% by weight and more preferably 1.0 to 3% by weight, based on the composition.
Alkali metal hydroxides Suitable alkali metal hydroxides are potassium hydroxide and, in particular, sodium hydroxide which are used in quantities of preferably 0.5 to 2.0% by weight and more preferably 0.7 to 1.0% by weight, based on the composition, and of which the function is to adjust the pH of the compositions to an optimal value of 12.5 to 14Ø
Electrolyte salts Typical examples of suitable electrolyte salts are the alkali metal and alkaline earth metal carbonates, chlorides, silicates, phosphates and phosphonates and mixtures thereof. Sodium and potassium carbonate or chloride are preferably used. Not only do they buffer the composition as required, they also sequester metal ions and, more particularly, heavy metal ions. Another advantage is their low price and the ease with which they can be incorporated. The electrolyte salts are used in quantities of preferably 1.0 to 2.0% by weight, based on the composition.
Fatty acid salts The compositions according to the invention may additionally 5 contain fatty acid salts corresponding to formula (III):
R5C0-OX (III) in which R5C0 is an acyl group containing 12 to 22 carbon atoms and X is an alkali metal. Typical examples are the sodium and/or potassium salts of lauric acid, myristic acid, palmitic acid, palmitoleic acid, stearic acid, isostearic acid, oleic acid, elaidic acid, petroselic acid, linoleic acid, linolenic acid, elaeostearic acid, arachic acid, gadoleic acid, behenic acid and erucic acid and the technical mixtures thereof obtained in the pressure hydrolysis of technical fats and oils. Salts of technical cocofatty acid or tallow fatty acid are preferably used. Since the formulations according to the invention are highly alkaline, the salts may also be replaced by the fatty acids which are neutralized in situ on introduction into the mixture. The fatty acid salts are used in quantities of preferably 0.5 to 2.0% by weight, based on the composition.
Commercial Applications Additional auxiliaries and additives which may be used in accord ance with the invention include, for example, chlorine-stable surfactants and hydrotropes such as, for example, alkyl sulfates, alkyl sulfonates, alkyl benzenesulfonates, xylene sulfonates, sarcosinates, taurides, isethionates, sulfosuccinates, betaines, sugar esters, fatty alcohol polyglycol ethers, alkyl oligoglycosides and fatty acid-N-alkyl glucamides and the ether carboxylates obtainable, for example, by alkoxylation of alcohols with ethylene oxide or propylene oxide as sole alkoxide or with several alkoxides and subsequent oxidation. It is particularly preferred to use alkyl sulfates in quantities of 0.5 to 3% by weight. In one preferred embodiment, all the surfactants together make up at most 10 to 15% by weight of the total quantity of ingredients in the formulation. The compositions according to the invention may contain alkali metal compounds, preferably sodium hydroxide or potassium hydroxide, with which the pH of the formulations can be adjusted to an optimal value of 10 to 14 and preferably 12.5 to 13.5.
In addition, the compositions may contain other active-chlorine-stable perfumes, optical brighteners, sequestrants, dyes and pigments in total quantities of 0.01 to 5.0% by weight, based on the composition.
Typical examples of suitable optical brighteners are derivatives of diaminostilbene disulfonic acid and alkali metal salts thereof. Suitable optical brighteners are, for example, derivatives of 4,4'-diamino-2,2'-stilbene disulfonic acid (flavonic acid), such as in particular the salts of 4,4'-bis-(2-anilino-4-morpholino-1,3,5-triazinyl-6-amino)-stillbene-2,2'-disulfonic acid or compounds of similar structure which, instead of the morpholi~no group, contain a diethanolamino group, a methylamino group, an anilino group or a 2-methoxyethylamino group. Other brighteners which may be present are those of the substituted diphenyl styryl type, for example alkali metal salts of 4,4'-bis-(2-sulfostyryl)-diphenyl, 4,4'-bis-(4-chloro-3-sulfostyryl)-Biphenyl or 4-(4-chlorostyryl)-4'-(2-sulfostyryl)-Biphenyl, methyl umbelliferone, coumarin, dihydroquinolinone, 1,3-diaryl pyrazoline, naphthalic acid amide, benzoxazole, benzisoxazole and benzimidazole systems linked by CH=CH bonds, heterocycle-substituted pyrine derivatives and the like. Mixtures of the brighteners mentioned above may also be used. The potassium salt of 4,4'-bis-(1,2,3-triazolyl)-(2)-stilbine-2,2-sulfonic acid marketed under the name of Phorwite~ BHC 766 is particularly preferred. The compositions generally contain the optical brighteners in quantities of 1 to 5% by weight and preferably 2 to 3% by weight. Blue dyes may also be present in small quantities. Particularly preferred brighteners/dyes are naphthotriazole stilbene sulfonic acid, for example in the form of its sodium salt (Tinopal~ RBS 200), and tetrabenzoazaporphine (Tinolux~ BBS), distyryl biphenyl bis-(triazinylamino)-stilbene disulfonic acid (Tinopal~ CDS-X) and, in particular, 4,4'-bis-(2-sulfostyryl)-biphenyl disodium salt (Tinopal~ CBS-X, products of Ciba).
Typical examples of suitable perfumes stable to active chlorine are: citronellol (3,7-dimethyl-6-octen-1-ol), dimethyl octanol (3,7-dimethyl-1-octanol), hydroxycitronellol (3,7-dimethyloctane-1,7-diol), mugol (3,7-dimethyl-4,6-octatrien-3-ol), myrcenol (2-methyl-6-methylene-7-octen-2-ol), tetrahydromyrcenol (THM, 2,6-dimethyloctan-2-ol), terpinolene (p-mentho-1,4-(8)-diene), ethyl-2-methyl butyrate, phenyl propyl alcohol, galaxolide (1,3,4,6,7,8-hexahydro-4,6,6,7,8,8-hexamethyl cyclopental-2-benzopyran), tonalide (7-acetyl-1,1,3,4,4,6-hexamethyl tetrahydronaphthalene), rose oxide, linalol oxide, 2,6-dimethyl-3-octanol, tetrahydroethyl linalool, tetrahydroethyl linalyl acetate, o-sec.-butyl cyclohexyl acetate and isolone diphorenepoxide and also isoborneal, dihydroterpineol, isobornyl acetate, dihydroterpenyl acetate. Other suitable perfumes are the substances mentioned in columns 3 and 4 of European patent application EP 0 622 451 A1 (Procter & Gamble).
In addition, the compositions contain polyacrylates, amine oxide phosphonic acids and lignin sulfonates and mixtures thereof, for example the modified polyacrylate Norasol~ 470 N (Rohm & Haas, Germany), a polyphosphonoacrylate with a molecular weight of 3500 dalton, as sequestrants in quantities of 0.1 to 2.0% by weight and preferably 0.5 to 1.0% by weight, based on the composition.
Suitable pigments are inter alia green chlorophthalocyanines (Pigmosol~ Green, Hostaphine~ Green) or yellow Solar Yellow BG 300 (Sandoz).
The compositions according to the invention are prepared by stirring. The product obtained may optionally be decanted or filtered to remove foreign bodies and/or agglomerates. The compositions preferably have a viscosity (as measured at 20°C in a Brookfield LV viscosimeter, spindle 1, 60 r.p.m.) below 50 mPas, preferably no more than 40 mPas, more preferably no more than 20 mPas and, in one particularly preferred embodiment, no more than 10 mPas and/or a foam height below 100 mm, preferably no more than 60 mm and more preferably no more than 40 mm, as measured by the Ross-Miles test at 20°C.
Examples Viscosity was measured at 20°C using a Brookfield viscosimeter (model LVT, spindle 1, 60 r.p.m.) while foaming behavior was determined by the Ross-Miles test. Formulations 1 to 4 correspond to the invention while formulations C1 and C2 are intended for comparison. The results are set out in Table 1 (quantities in % by weight).
Table 1 Performance properties ,. .
5.4.
Sodium hypochlorite 3.8 3.8 3.8 3.8 3.8 3.8 Sodium hydroxide 0.850.85 0.85 0.850.85 0.85 Cocofatty alcohol +2E0 sulfate0.300.50 1.0 1.0 1.0 1.0 Na salt Amidoamine oxide's 1.252.0 1.25 2.3 - -Amine oxide2~ - - - - - 2.3 Water to Brookfield Viscosity [mPas] 15 15 40 20 150 50 Foam height in the Ross-Miles test [mm]
- Basicfoam (after0 min.) 35 38 60 60 120 100 _ _ - After 5 mins. I 30 20 35 55 110 ~
I I I ~ 90 '~ Basis: condensation product of cocofatty acid and ethylenediamine 2~ Basis: methyl dicocoylamine
Background of the Invention In the past, bleaching compositions based on alkali metal hypo-chlorites which have a remarkable viscosity and which are therefore suitable both for the treatment of horizontal surfaces and for the treatment of sloping and, above all, vertical surfaces have been successfully used in the field of hygiene and disinfection and in the textile treatment field. The effect of the high viscosity of these compositions is that the contact time between them and the surfaces to be treated is considerably longer than in the case of commercially available liquid products which soon flow off the surface.
Various publications relating to such viscous bleaching and disinfecting compositions are known from the literature. A few patents on this subject are mentioned by way of example in the following.
EP 0 274 885 A (ICI), for example, recommends the use of mixtures of linear and branched amine oxides. ES 88 01 389 A (Henkel Iberica) relates to bleaching compositions based on aqueous hypochlorite solutions which predominantly contain alkyl ether sulfates and, in addition, small amounts of amine oxides as their surfactant component. In DE 43 33 100 C1, applicants describe stable and sufficiently viscous aqueous bleaching and cleaning compositions based on hypochlorites, fatty alcohol ether sulfates and amine oxides which contain as a compulsory component amine oxide phosphonic acids which make a crucial contribution towards the thickening the compositions.
In practice, the viscosity of the hypochlorite solutions known from the literature is often too high for cleaning hard surfaces (viscosities of 50 mPas and higher, as measured in a Brookfield LV viscosimeter at 20°C, spindle 1, 60 r.p.m.). In addition, the excessive foaming (foam heights of 100 mm and more, as measured by the Ross-Miles test at 20°C) is often regarded as problematical. Compared with the hitherto known products, less expensive bleaching and disinfecting compositions would also be desirable.
Accordingly, the problem addressed by the present invention was to provide new water-containing bleaching and disinfecting compositions which would generate less foam and would be less viscous than the known compositions. Finally, another problem addressed by the invention was to provide compositions which would be distinguished by a price advantage over the hitherto known hypochlorite bleaching compositions.
Description of the Invention The present invention relates to bleaching and disinfecting compositions containing - based on the composition -(a) 1.0 to 6.0% by weight alkali metal hypochlorites, (b) 0.1 to 5.0% by weight alkyl ether sulfates, (c) 0.5 to 5.0% by weight amidoamine oxides and (d) 0.5 to 2.0% by weight alkali metal hydroxides, with the proviso that the quantities shown add up to 100% by weight with water and, optionally, other auxiliaries and additives.
It has surprisingly been found that the addition of amidoamine oxides to bleaching and disinfecting compositions reduces not only their viscosity, but also their foaming. Viscosities below 50 mPas (Brookfield LVT viscosimeter, 20°C, spindle 1, 60 r.p.m.) and foam heights below 100 mm (Ross-Miles test, 20°C) have been measured for the compositions according to the invention. In addition, the amidoamine oxides used in the mixture represent a much more favorably priced alternative to the amine oxides conventionally used.
Alkali metal hypochlorites Alkali metal hypochlorites in the context of the present invention are lithium, potassium and, in particular, sodium hypochlorite. The hypochlo-rites may advantageously be used in quantities of 1.0 to 6.0% by weight and preferably in quantities of 3.0 to 5.0% by weight, based on the composition.
Alkyl ether sulfates Alkyl ether sulfates are known anionic surfactants which may be obtained by sulfation of nonionic surfactants of the alkyl polyglycol ether type and subsequent neutralization. Alkyl ether sulfates suitable for use in the compositions according to the invention correspond to formula (I):
R'O-(CH2CH2O)"SO3X (~) in which R' is an alkyl group containing 12 to 18 carbon atoms, n is a number of 2 to 5 and X represents sodium or potassium. Typical examples are the sodium salts of sulfates of the C~2,~4 cocofatty alcohol 2 EO, 2.3 EO
and 3 EO adduct. The alkyl ether sulfates may have a conventional or narrow homolog distribution. The alkyl ether sulfates are used in quantities of preferably 0.1 to 5.0% by weight and more preferably 0.2 to 1.5% by weight, based on the composition.
Amidoamine oxides Amidoamine oxides are known substances which are occasionally classed as cationic surfactants, but generally as nonionic surfactants.
They are produced from tertiary fatty acid amidoamines of which the anionic nitrogen is oxidized with hydrogen peroxide. The amidoamine oxides suitable for use in accordance with the invention correspond to formula (II):
R2CONH(CH2)", i ->O (II) in which R2C0 is a linear or branched acyl group containing 12 to 18 carbon atoms, R3 and R4 independently of one another represent an optionally hydroxysubstituted alkyl group containing 1 to 4 carbon atoms and m is a number of 1 to 3. Amidoamine oxides corresponding to formula (11), in which R2C0 is a cocoacyl group, R3 and R4 represent a methyl or a hydroxyethyl group and m has a value of 2, are preferably used. The amidoamine oxides are used in quantities of preferably 0.5 to 5.0% by weight and more preferably 1.0 to 3% by weight, based on the composition.
Alkali metal hydroxides Suitable alkali metal hydroxides are potassium hydroxide and, in particular, sodium hydroxide which are used in quantities of preferably 0.5 to 2.0% by weight and more preferably 0.7 to 1.0% by weight, based on the composition, and of which the function is to adjust the pH of the compositions to an optimal value of 12.5 to 14Ø
Electrolyte salts Typical examples of suitable electrolyte salts are the alkali metal and alkaline earth metal carbonates, chlorides, silicates, phosphates and phosphonates and mixtures thereof. Sodium and potassium carbonate or chloride are preferably used. Not only do they buffer the composition as required, they also sequester metal ions and, more particularly, heavy metal ions. Another advantage is their low price and the ease with which they can be incorporated. The electrolyte salts are used in quantities of preferably 1.0 to 2.0% by weight, based on the composition.
Fatty acid salts The compositions according to the invention may additionally 5 contain fatty acid salts corresponding to formula (III):
R5C0-OX (III) in which R5C0 is an acyl group containing 12 to 22 carbon atoms and X is an alkali metal. Typical examples are the sodium and/or potassium salts of lauric acid, myristic acid, palmitic acid, palmitoleic acid, stearic acid, isostearic acid, oleic acid, elaidic acid, petroselic acid, linoleic acid, linolenic acid, elaeostearic acid, arachic acid, gadoleic acid, behenic acid and erucic acid and the technical mixtures thereof obtained in the pressure hydrolysis of technical fats and oils. Salts of technical cocofatty acid or tallow fatty acid are preferably used. Since the formulations according to the invention are highly alkaline, the salts may also be replaced by the fatty acids which are neutralized in situ on introduction into the mixture. The fatty acid salts are used in quantities of preferably 0.5 to 2.0% by weight, based on the composition.
Commercial Applications Additional auxiliaries and additives which may be used in accord ance with the invention include, for example, chlorine-stable surfactants and hydrotropes such as, for example, alkyl sulfates, alkyl sulfonates, alkyl benzenesulfonates, xylene sulfonates, sarcosinates, taurides, isethionates, sulfosuccinates, betaines, sugar esters, fatty alcohol polyglycol ethers, alkyl oligoglycosides and fatty acid-N-alkyl glucamides and the ether carboxylates obtainable, for example, by alkoxylation of alcohols with ethylene oxide or propylene oxide as sole alkoxide or with several alkoxides and subsequent oxidation. It is particularly preferred to use alkyl sulfates in quantities of 0.5 to 3% by weight. In one preferred embodiment, all the surfactants together make up at most 10 to 15% by weight of the total quantity of ingredients in the formulation. The compositions according to the invention may contain alkali metal compounds, preferably sodium hydroxide or potassium hydroxide, with which the pH of the formulations can be adjusted to an optimal value of 10 to 14 and preferably 12.5 to 13.5.
In addition, the compositions may contain other active-chlorine-stable perfumes, optical brighteners, sequestrants, dyes and pigments in total quantities of 0.01 to 5.0% by weight, based on the composition.
Typical examples of suitable optical brighteners are derivatives of diaminostilbene disulfonic acid and alkali metal salts thereof. Suitable optical brighteners are, for example, derivatives of 4,4'-diamino-2,2'-stilbene disulfonic acid (flavonic acid), such as in particular the salts of 4,4'-bis-(2-anilino-4-morpholino-1,3,5-triazinyl-6-amino)-stillbene-2,2'-disulfonic acid or compounds of similar structure which, instead of the morpholi~no group, contain a diethanolamino group, a methylamino group, an anilino group or a 2-methoxyethylamino group. Other brighteners which may be present are those of the substituted diphenyl styryl type, for example alkali metal salts of 4,4'-bis-(2-sulfostyryl)-diphenyl, 4,4'-bis-(4-chloro-3-sulfostyryl)-Biphenyl or 4-(4-chlorostyryl)-4'-(2-sulfostyryl)-Biphenyl, methyl umbelliferone, coumarin, dihydroquinolinone, 1,3-diaryl pyrazoline, naphthalic acid amide, benzoxazole, benzisoxazole and benzimidazole systems linked by CH=CH bonds, heterocycle-substituted pyrine derivatives and the like. Mixtures of the brighteners mentioned above may also be used. The potassium salt of 4,4'-bis-(1,2,3-triazolyl)-(2)-stilbine-2,2-sulfonic acid marketed under the name of Phorwite~ BHC 766 is particularly preferred. The compositions generally contain the optical brighteners in quantities of 1 to 5% by weight and preferably 2 to 3% by weight. Blue dyes may also be present in small quantities. Particularly preferred brighteners/dyes are naphthotriazole stilbene sulfonic acid, for example in the form of its sodium salt (Tinopal~ RBS 200), and tetrabenzoazaporphine (Tinolux~ BBS), distyryl biphenyl bis-(triazinylamino)-stilbene disulfonic acid (Tinopal~ CDS-X) and, in particular, 4,4'-bis-(2-sulfostyryl)-biphenyl disodium salt (Tinopal~ CBS-X, products of Ciba).
Typical examples of suitable perfumes stable to active chlorine are: citronellol (3,7-dimethyl-6-octen-1-ol), dimethyl octanol (3,7-dimethyl-1-octanol), hydroxycitronellol (3,7-dimethyloctane-1,7-diol), mugol (3,7-dimethyl-4,6-octatrien-3-ol), myrcenol (2-methyl-6-methylene-7-octen-2-ol), tetrahydromyrcenol (THM, 2,6-dimethyloctan-2-ol), terpinolene (p-mentho-1,4-(8)-diene), ethyl-2-methyl butyrate, phenyl propyl alcohol, galaxolide (1,3,4,6,7,8-hexahydro-4,6,6,7,8,8-hexamethyl cyclopental-2-benzopyran), tonalide (7-acetyl-1,1,3,4,4,6-hexamethyl tetrahydronaphthalene), rose oxide, linalol oxide, 2,6-dimethyl-3-octanol, tetrahydroethyl linalool, tetrahydroethyl linalyl acetate, o-sec.-butyl cyclohexyl acetate and isolone diphorenepoxide and also isoborneal, dihydroterpineol, isobornyl acetate, dihydroterpenyl acetate. Other suitable perfumes are the substances mentioned in columns 3 and 4 of European patent application EP 0 622 451 A1 (Procter & Gamble).
In addition, the compositions contain polyacrylates, amine oxide phosphonic acids and lignin sulfonates and mixtures thereof, for example the modified polyacrylate Norasol~ 470 N (Rohm & Haas, Germany), a polyphosphonoacrylate with a molecular weight of 3500 dalton, as sequestrants in quantities of 0.1 to 2.0% by weight and preferably 0.5 to 1.0% by weight, based on the composition.
Suitable pigments are inter alia green chlorophthalocyanines (Pigmosol~ Green, Hostaphine~ Green) or yellow Solar Yellow BG 300 (Sandoz).
The compositions according to the invention are prepared by stirring. The product obtained may optionally be decanted or filtered to remove foreign bodies and/or agglomerates. The compositions preferably have a viscosity (as measured at 20°C in a Brookfield LV viscosimeter, spindle 1, 60 r.p.m.) below 50 mPas, preferably no more than 40 mPas, more preferably no more than 20 mPas and, in one particularly preferred embodiment, no more than 10 mPas and/or a foam height below 100 mm, preferably no more than 60 mm and more preferably no more than 40 mm, as measured by the Ross-Miles test at 20°C.
Examples Viscosity was measured at 20°C using a Brookfield viscosimeter (model LVT, spindle 1, 60 r.p.m.) while foaming behavior was determined by the Ross-Miles test. Formulations 1 to 4 correspond to the invention while formulations C1 and C2 are intended for comparison. The results are set out in Table 1 (quantities in % by weight).
Table 1 Performance properties ,. .
5.4.
Sodium hypochlorite 3.8 3.8 3.8 3.8 3.8 3.8 Sodium hydroxide 0.850.85 0.85 0.850.85 0.85 Cocofatty alcohol +2E0 sulfate0.300.50 1.0 1.0 1.0 1.0 Na salt Amidoamine oxide's 1.252.0 1.25 2.3 - -Amine oxide2~ - - - - - 2.3 Water to Brookfield Viscosity [mPas] 15 15 40 20 150 50 Foam height in the Ross-Miles test [mm]
- Basicfoam (after0 min.) 35 38 60 60 120 100 _ _ - After 5 mins. I 30 20 35 55 110 ~
I I I ~ 90 '~ Basis: condensation product of cocofatty acid and ethylenediamine 2~ Basis: methyl dicocoylamine
Claims (17)
1. Bleaching and disinfecting compositions comprising:
a) 1.0 to 6.0 percent by weight of an alkali metal hypochlorite;
b) 0.1 to 5.0 percent by weight of an alkyl ether sulfate;
c) 0.5 to 5.0 percent by weight of an amidoamine oxide; and d) 0.5 to 2.0 percent by weight of an alkali metal hydroxide.
a) 1.0 to 6.0 percent by weight of an alkali metal hypochlorite;
b) 0.1 to 5.0 percent by weight of an alkyl ether sulfate;
c) 0.5 to 5.0 percent by weight of an amidoamine oxide; and d) 0.5 to 2.0 percent by weight of an alkali metal hydroxide.
2. The composition of claim 1 wherein said alkali metal hypochlorite comprises sodium hypochlorite.
3. The composition of claim 1 comprising 3.0 to 5.0 percent by weight of said alkali metal hypochlorite.
4. The composition of claim 1 comprising an alkyl ether sulfate corresponding to formula (I):
R1O-(CH2CH2O)nSO3X (I) wherein R1 is an alkyl group containing 12 to 18 carbon atoms, n is a number of 2 to 5, and X is sodium or potassium.
R1O-(CH2CH2O)nSO3X (I) wherein R1 is an alkyl group containing 12 to 18 carbon atoms, n is a number of 2 to 5, and X is sodium or potassium.
5. The composition of claim 1 comprising 0.2 to 1.5 percent by weight of said alkyl ether sulfate.
6. The composition of claim 1 comprising an amidoamine oxides corresponding to formula (II):
wherein R2CO is a linear or branched acyl group containing 12 to 18 carbon atoms, R3 and R4 independently of one another represent an optionally hydroxysubstituted alkyl group containing 1 to 4 carbon atoms, and m is a number of 1 to 3.
wherein R2CO is a linear or branched acyl group containing 12 to 18 carbon atoms, R3 and R4 independently of one another represent an optionally hydroxysubstituted alkyl group containing 1 to 4 carbon atoms, and m is a number of 1 to 3.
7. The composition of claim 1 comprising 1.0 to 3 percent by weight of said amidoamine oxide.
8. The composition of claim 1 wherein said alkali metal hydroxide comprises sodium hydroxide.
9. The composition of claim 1 comprising 0.7 to 1.0 percent by weight of said alkali metal hydroxide.
10. The composition of claim 1 having a pH of from 12.5 to 14Ø
11. The composition of claim 1 further comprising an electrolyte salt selected from the group consisting of alkali metal carbonates, alkaline earth metal carbonates, chlorides, silicates, phosphates, phosphonates, and mixtures thereof.
12. The composition of claim 11 comprising 1.0 to 2.0 percent by weight of said electrolyte salt.
13. The composition of claim 1 further comprising a fatty acid salt corresponding to formula (III):
R5CO-OX (III) wherein R5CO is an acyl group containing 12 to 22 carbon atoms, and X is an alkali metal.
R5CO-OX (III) wherein R5CO is an acyl group containing 12 to 22 carbon atoms, and X is an alkali metal.
14. The composition of claim 13 comprising 0.5 to 2.0 percent by weight of said fatty acid salt.
15. The composition of claim 1 further comprising a sequestrant selected from the group consisting of polyacrylates, amine oxide phosphonic acids, lignin sulfonates, and mixtures thereof.
16. The composition of claim 1 having a viscosity below 50 mPas, as measured at 20°C in a Brookfield viscometer immediately after its production.
17. The composition of claim 1 having a foam height below 100 mm, as measured at 20°C by the Ross-miles test immediately after its production.
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
DE1999102904 DE19902904A1 (en) | 1999-01-26 | 1999-01-26 | Bleach and disinfectant |
DE19902904.0 | 1999-01-26 |
Publications (1)
Publication Number | Publication Date |
---|---|
CA2297223A1 true CA2297223A1 (en) | 2000-07-26 |
Family
ID=7895349
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
CA 2297223 Abandoned CA2297223A1 (en) | 1999-01-26 | 2000-01-26 | Bleaching and disinfecting compositions |
Country Status (4)
Country | Link |
---|---|
AU (1) | AU2664200A (en) |
CA (1) | CA2297223A1 (en) |
DE (1) | DE19902904A1 (en) |
WO (1) | WO2000044865A1 (en) |
Family Cites Families (6)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
CA1226213A (en) * | 1982-09-24 | 1987-09-01 | Johnson & Johnson Baby Products Company | Antimicrobial compositions |
CA2171709C (en) * | 1993-09-20 | 1999-12-21 | Panos Iakovides | Thickened aqueous detergent compositions with improved cleaning performance |
DE4333100C1 (en) * | 1993-09-29 | 1994-10-06 | Henkel Kgaa | Bleaching and disinfecting compositions |
DE19621048C2 (en) * | 1996-05-24 | 2000-06-21 | Henkel Kgaa | Aqueous bleach and disinfectant |
DE19626906C1 (en) * | 1996-07-04 | 1998-03-12 | Henkel Kgaa | Means for cleaning hard surfaces |
GB2322379A (en) * | 1997-02-24 | 1998-08-26 | Reckitt & Colman South Africa | Abrasive bleach containing composition |
-
1999
- 1999-01-26 DE DE1999102904 patent/DE19902904A1/en not_active Ceased
-
2000
- 2000-01-15 AU AU26642/00A patent/AU2664200A/en not_active Abandoned
- 2000-01-15 WO PCT/EP2000/000283 patent/WO2000044865A1/en active Application Filing
- 2000-01-26 CA CA 2297223 patent/CA2297223A1/en not_active Abandoned
Also Published As
Publication number | Publication date |
---|---|
WO2000044865A1 (en) | 2000-08-03 |
AU2664200A (en) | 2000-08-18 |
DE19902904A1 (en) | 2000-08-03 |
Similar Documents
Publication | Publication Date | Title |
---|---|---|
US6204235B1 (en) | Active chlorine preparations containing stabilized optical brighteners | |
US6090770A (en) | Aqueous bleaching agents | |
CA2080688C (en) | Liquid detergent compositions | |
HU214669B (en) | Process for producing liquid detergent compositions | |
US5384061A (en) | Stable thickened aqueous cleaning composition containing a chlorine bleach and phytic acid | |
AU643849B2 (en) | Detergent compositions | |
US6221827B1 (en) | Viscoelastic bleaching and disinfecting compostions | |
CH660374A5 (en) | STABILIZED, CLEAR, SINGLE-PHASE, BUILDER AND ENZYME-CONTAINING LIQUID DETERGENT. | |
EP0346993A2 (en) | Liquid detergent compositions | |
NZ201708A (en) | Low viscosity built bleaching liquid detergent compositions | |
AU627228B2 (en) | Liquid detergent compositions | |
EP0808359A1 (en) | Liquid compositions | |
EP0346994B1 (en) | Liquid detergent compositions | |
CA2297223A1 (en) | Bleaching and disinfecting compositions | |
US5672580A (en) | Liquid detergent compositions | |
CA2311485A1 (en) | Bleaching and disinfecting compositions | |
CA2073563C (en) | Liquid bleach composition | |
CA2291871A1 (en) | Active chlorine preparations containing stabilized perfumes | |
CA2064900C (en) | Liquid detergents | |
EP0491723B1 (en) | Liquid detergents | |
CA2299178A1 (en) | Active chlorine preparations containing microencapsulated colorants | |
AU7187491A (en) | Liquid bleach composition | |
WO1997039098A1 (en) | Fabric treatment composition containing thickened hydrogen peroxide solution | |
CZ248299A3 (en) | Aqueous bleaching preparations | |
SK562000A3 (en) | Use of electrolyte mixtures as sequestering agents |
Legal Events
Date | Code | Title | Description |
---|---|---|---|
FZDE | Dead |