SK58599A3 - Liquid aqueous bleaching compositions and pretreatment process - Google Patents
Liquid aqueous bleaching compositions and pretreatment process Download PDFInfo
- Publication number
- SK58599A3 SK58599A3 SK585-99A SK58599A SK58599A3 SK 58599 A3 SK58599 A3 SK 58599A3 SK 58599 A SK58599 A SK 58599A SK 58599 A3 SK58599 A3 SK 58599A3
- Authority
- SK
- Slovakia
- Prior art keywords
- group
- alkyl
- composition
- caprolactam
- cationic
- Prior art date
Links
- 239000000203 mixture Substances 0.000 title claims abstract description 244
- 238000000034 method Methods 0.000 title claims abstract description 28
- 238000004061 bleaching Methods 0.000 title claims description 29
- 239000007788 liquid Substances 0.000 title claims description 28
- 230000008569 process Effects 0.000 title abstract description 7
- -1 ethoxylated cationic diamine Chemical class 0.000 claims abstract description 129
- 239000007844 bleaching agent Substances 0.000 claims abstract description 72
- 229920000642 polymer Polymers 0.000 claims abstract description 71
- 239000004744 fabric Substances 0.000 claims abstract description 64
- 125000002091 cationic group Chemical group 0.000 claims abstract description 38
- 229920000768 polyamine Polymers 0.000 claims abstract description 32
- 239000002689 soil Substances 0.000 claims abstract description 15
- 239000003795 chemical substances by application Substances 0.000 claims description 56
- 239000004094 surface-active agent Substances 0.000 claims description 47
- 239000012535 impurity Substances 0.000 claims description 39
- 239000012190 activator Substances 0.000 claims description 28
- 125000002768 hydroxyalkyl group Chemical group 0.000 claims description 24
- 239000002253 acid Substances 0.000 claims description 23
- 229920006317 cationic polymer Polymers 0.000 claims description 20
- MHAJPDPJQMAIIY-UHFFFAOYSA-N Hydrogen peroxide Chemical compound OO MHAJPDPJQMAIIY-UHFFFAOYSA-N 0.000 claims description 19
- 239000002738 chelating agent Substances 0.000 claims description 17
- 239000000839 emulsion Substances 0.000 claims description 17
- 229910052739 hydrogen Inorganic materials 0.000 claims description 17
- 238000005406 washing Methods 0.000 claims description 17
- RTZKZFJDLAIYFH-UHFFFAOYSA-N Diethyl ether Chemical compound CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 claims description 16
- 150000001412 amines Chemical class 0.000 claims description 15
- 125000004450 alkenylene group Chemical group 0.000 claims description 14
- 125000005702 oxyalkylene group Chemical group 0.000 claims description 14
- 239000002904 solvent Substances 0.000 claims description 14
- 229910052799 carbon Inorganic materials 0.000 claims description 13
- 229920000728 polyester Polymers 0.000 claims description 12
- 125000000732 arylene group Chemical group 0.000 claims description 11
- 239000004530 micro-emulsion Substances 0.000 claims description 11
- 125000003118 aryl group Chemical group 0.000 claims description 9
- 239000004952 Polyamide Substances 0.000 claims description 8
- 239000000975 dye Substances 0.000 claims description 8
- 229920002647 polyamide Polymers 0.000 claims description 8
- 239000000370 acceptor Substances 0.000 claims description 7
- 125000003342 alkenyl group Chemical group 0.000 claims description 7
- 229920001281 polyalkylene Polymers 0.000 claims description 7
- WEAPVABOECTMGR-UHFFFAOYSA-N triethyl 2-acetyloxypropane-1,2,3-tricarboxylate Chemical group CCOC(=O)CC(C(=O)OCC)(OC(C)=O)CC(=O)OCC WEAPVABOECTMGR-UHFFFAOYSA-N 0.000 claims description 7
- 229920002635 polyurethane Polymers 0.000 claims description 6
- 239000004814 polyurethane Substances 0.000 claims description 6
- 229920000058 polyacrylate Polymers 0.000 claims description 5
- 229920000570 polyether Polymers 0.000 claims description 5
- 239000003381 stabilizer Substances 0.000 claims description 5
- 238000012546 transfer Methods 0.000 claims description 5
- 150000004965 peroxy acids Chemical class 0.000 claims description 4
- 229920002401 polyacrylamide Polymers 0.000 claims description 4
- 229920001289 polyvinyl ether Polymers 0.000 claims description 4
- 239000004642 Polyimide Substances 0.000 claims description 3
- 125000002877 alkyl aryl group Chemical group 0.000 claims description 3
- 239000003086 colorant Substances 0.000 claims description 3
- 150000002432 hydroperoxides Chemical class 0.000 claims description 3
- 239000002304 perfume Substances 0.000 claims description 3
- 229920001721 polyimide Polymers 0.000 claims description 3
- 229920002717 polyvinylpyridine Polymers 0.000 claims description 3
- JGBAASVQPMTVHO-UHFFFAOYSA-N 2,5-dihydroperoxy-2,5-dimethylhexane Chemical compound OOC(C)(C)CCC(C)(C)OO JGBAASVQPMTVHO-UHFFFAOYSA-N 0.000 claims description 2
- XRXANEMIFVRKLN-UHFFFAOYSA-N 2-hydroperoxy-2-methylbutane Chemical compound CCC(C)(C)OO XRXANEMIFVRKLN-UHFFFAOYSA-N 0.000 claims description 2
- FAGGUIDTQQXDSJ-UHFFFAOYSA-N 3-benzoylazepan-2-one Chemical class C=1C=CC=CC=1C(=O)C1CCCCNC1=O FAGGUIDTQQXDSJ-UHFFFAOYSA-N 0.000 claims description 2
- AVLQNPBLHZMWFC-UHFFFAOYSA-N 6-(nonylamino)-6-oxohexaneperoxoic acid Chemical compound CCCCCCCCCNC(=O)CCCCC(=O)OO AVLQNPBLHZMWFC-UHFFFAOYSA-N 0.000 claims description 2
- QISSLHPKTCLLDL-UHFFFAOYSA-N N-Acetylcaprolactam Chemical compound CC(=O)N1CCCCCC1=O QISSLHPKTCLLDL-UHFFFAOYSA-N 0.000 claims description 2
- 125000005024 alkenyl aryl group Chemical group 0.000 claims description 2
- 125000001797 benzyl group Chemical group [H]C1=C([H])C([H])=C(C([H])=C1[H])C([H])([H])* 0.000 claims description 2
- 230000000295 complement effect Effects 0.000 claims description 2
- YQHLDYVWEZKEOX-UHFFFAOYSA-N cumene hydroperoxide Chemical compound OOC(C)(C)C1=CC=CC=C1 YQHLDYVWEZKEOX-UHFFFAOYSA-N 0.000 claims description 2
- 239000012933 diacyl peroxide Substances 0.000 claims description 2
- 125000001033 ether group Chemical group 0.000 claims description 2
- YDLQSTFHBCVEJV-UHFFFAOYSA-M sodium;2-(3,5,5-trimethylhexanoyloxy)benzenesulfonate Chemical compound [Na+].CC(C)(C)CC(C)CC(=O)OC1=CC=CC=C1S([O-])(=O)=O YDLQSTFHBCVEJV-UHFFFAOYSA-M 0.000 claims description 2
- JBKVHLHDHHXQEQ-UHFFFAOYSA-N Caprolactam Natural products O=C1CCCCCN1 JBKVHLHDHHXQEQ-UHFFFAOYSA-N 0.000 claims 14
- UHGWBEXBBNLGCZ-UHFFFAOYSA-N phenyl nonanoate Chemical compound CCCCCCCCC(=O)OC1=CC=CC=C1 UHGWBEXBBNLGCZ-UHFFFAOYSA-N 0.000 claims 2
- CIHOLLKRGTVIJN-UHFFFAOYSA-N tert‐butyl hydroperoxide Chemical compound CC(C)(C)OO CIHOLLKRGTVIJN-UHFFFAOYSA-N 0.000 claims 2
- YIVJZNGAASQVEM-UHFFFAOYSA-N Lauroyl peroxide Chemical compound CCCCCCCCCCCC(=O)OOC(=O)CCCCCCCCCCC YIVJZNGAASQVEM-UHFFFAOYSA-N 0.000 claims 1
- 239000004793 Polystyrene Substances 0.000 claims 1
- 239000004372 Polyvinyl alcohol Substances 0.000 claims 1
- XJOBOFWTZOKMOH-UHFFFAOYSA-N decanoyl decaneperoxoate Chemical compound CCCCCCCCCC(=O)OOC(=O)CCCCCCCCC XJOBOFWTZOKMOH-UHFFFAOYSA-N 0.000 claims 1
- 239000004088 foaming agent Substances 0.000 claims 1
- 125000004836 hexamethylene group Chemical group [H]C([H])([*:2])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])[*:1] 0.000 claims 1
- 229920002223 polystyrene Polymers 0.000 claims 1
- 229920002451 polyvinyl alcohol Polymers 0.000 claims 1
- MWNQXXOSWHCCOZ-UHFFFAOYSA-L sodium;oxido carbonate Chemical compound [Na+].[O-]OC([O-])=O MWNQXXOSWHCCOZ-UHFFFAOYSA-L 0.000 claims 1
- FRPJTGXMTIIFIT-UHFFFAOYSA-N tetraacetylethylenediamine Chemical compound CC(=O)C(N)(C(C)=O)C(N)(C(C)=O)C(C)=O FRPJTGXMTIIFIT-UHFFFAOYSA-N 0.000 claims 1
- SLFUZVJZPBHLAQ-UHFFFAOYSA-N tetradecanoyl tetradecaneperoxoate Chemical compound CCCCCCCCCCCCCC(=O)OOC(=O)CCCCCCCCCCCCC SLFUZVJZPBHLAQ-UHFFFAOYSA-N 0.000 claims 1
- 230000002378 acidificating effect Effects 0.000 abstract description 19
- 239000000375 suspending agent Substances 0.000 abstract 1
- 125000000217 alkyl group Chemical group 0.000 description 32
- 230000002209 hydrophobic effect Effects 0.000 description 24
- 229920002873 Polyethylenimine Polymers 0.000 description 22
- 239000002736 nonionic surfactant Substances 0.000 description 19
- 150000001875 compounds Chemical class 0.000 description 18
- 125000002947 alkylene group Chemical group 0.000 description 15
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 description 15
- 150000002978 peroxides Chemical class 0.000 description 14
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 13
- 239000003599 detergent Substances 0.000 description 12
- 239000003945 anionic surfactant Substances 0.000 description 11
- 239000004927 clay Substances 0.000 description 11
- 125000004432 carbon atom Chemical group C* 0.000 description 10
- 238000004140 cleaning Methods 0.000 description 9
- 229910052757 nitrogen Inorganic materials 0.000 description 9
- 230000000694 effects Effects 0.000 description 8
- 230000002255 enzymatic effect Effects 0.000 description 8
- 238000007046 ethoxylation reaction Methods 0.000 description 8
- 239000000126 substance Substances 0.000 description 8
- 229920003171 Poly (ethylene oxide) Polymers 0.000 description 7
- 235000014113 dietary fatty acids Nutrition 0.000 description 7
- 150000002148 esters Chemical class 0.000 description 7
- 229930195729 fatty acid Natural products 0.000 description 7
- 239000000194 fatty acid Substances 0.000 description 7
- 150000004665 fatty acids Chemical class 0.000 description 7
- 239000004615 ingredient Substances 0.000 description 7
- 238000002360 preparation method Methods 0.000 description 7
- 150000003254 radicals Chemical class 0.000 description 7
- 150000001204 N-oxides Chemical class 0.000 description 6
- YDONNITUKPKTIG-UHFFFAOYSA-N [Nitrilotris(methylene)]trisphosphonic acid Chemical compound OP(O)(=O)CN(CP(O)(O)=O)CP(O)(O)=O YDONNITUKPKTIG-UHFFFAOYSA-N 0.000 description 6
- 150000007513 acids Chemical class 0.000 description 6
- 125000002252 acyl group Chemical group 0.000 description 6
- 125000003545 alkoxy group Chemical group 0.000 description 6
- 239000001913 cellulose Substances 0.000 description 6
- 229920002678 cellulose Polymers 0.000 description 6
- NEHMKBQYUWJMIP-UHFFFAOYSA-N chloromethane Chemical compound ClC NEHMKBQYUWJMIP-UHFFFAOYSA-N 0.000 description 6
- 230000001804 emulsifying effect Effects 0.000 description 6
- 239000001257 hydrogen Substances 0.000 description 6
- XMGQYMWWDOXHJM-UHFFFAOYSA-N limonene Chemical compound CC(=C)C1CCC(C)=CC1 XMGQYMWWDOXHJM-UHFFFAOYSA-N 0.000 description 6
- 238000006116 polymerization reaction Methods 0.000 description 6
- 229920000036 polyvinylpyrrolidone Polymers 0.000 description 6
- 235000013855 polyvinylpyrrolidone Nutrition 0.000 description 6
- 150000003839 salts Chemical class 0.000 description 6
- 229940071089 sarcosinate Drugs 0.000 description 6
- KKEYFWRCBNTPAC-UHFFFAOYSA-L terephthalate(2-) Chemical compound [O-]C(=O)C1=CC=C(C([O-])=O)C=C1 KKEYFWRCBNTPAC-UHFFFAOYSA-L 0.000 description 6
- LLLVZDVNHNWSDS-UHFFFAOYSA-N 4-methylidene-3,5-dioxabicyclo[5.2.2]undeca-1(9),7,10-triene-2,6-dione Chemical compound C1(C2=CC=C(C(=O)OC(=C)O1)C=C2)=O LLLVZDVNHNWSDS-UHFFFAOYSA-N 0.000 description 5
- 239000004215 Carbon black (E152) Substances 0.000 description 5
- KCXVZYZYPLLWCC-UHFFFAOYSA-N EDTA Chemical compound OC(=O)CN(CC(O)=O)CCN(CC(O)=O)CC(O)=O KCXVZYZYPLLWCC-UHFFFAOYSA-N 0.000 description 5
- 150000008051 alkyl sulfates Chemical class 0.000 description 5
- 125000000129 anionic group Chemical group 0.000 description 5
- 229940071106 ethylenediaminetetraacetate Drugs 0.000 description 5
- 229930195733 hydrocarbon Natural products 0.000 description 5
- 125000004435 hydrogen atom Chemical group [H]* 0.000 description 5
- 239000001267 polyvinylpyrrolidone Substances 0.000 description 5
- 235000000346 sugar Nutrition 0.000 description 5
- 150000003467 sulfuric acid derivatives Chemical class 0.000 description 5
- XMGQYMWWDOXHJM-JTQLQIEISA-N (+)-α-limonene Chemical compound CC(=C)[C@@H]1CCC(C)=CC1 XMGQYMWWDOXHJM-JTQLQIEISA-N 0.000 description 4
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 4
- DHMQDGOQFOQNFH-UHFFFAOYSA-N Glycine Chemical compound NCC(O)=O DHMQDGOQFOQNFH-UHFFFAOYSA-N 0.000 description 4
- AVXURJPOCDRRFD-UHFFFAOYSA-N Hydroxylamine Chemical compound ON AVXURJPOCDRRFD-UHFFFAOYSA-N 0.000 description 4
- 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 4
- 125000001931 aliphatic group Chemical group 0.000 description 4
- 229910052783 alkali metal Inorganic materials 0.000 description 4
- 150000003863 ammonium salts Chemical class 0.000 description 4
- YCIMNLLNPGFGHC-UHFFFAOYSA-N catechol Chemical compound OC1=CC=CC=C1O YCIMNLLNPGFGHC-UHFFFAOYSA-N 0.000 description 4
- 238000005119 centrifugation Methods 0.000 description 4
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- 125000001183 hydrocarbyl group Chemical group 0.000 description 4
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- 239000000178 monomer Substances 0.000 description 4
- 125000006353 oxyethylene group Chemical group 0.000 description 4
- 229920001601 polyetherimide Polymers 0.000 description 4
- YGSDEFSMJLZEOE-UHFFFAOYSA-N salicylic acid Chemical compound OC(=O)C1=CC=CC=C1O YGSDEFSMJLZEOE-UHFFFAOYSA-N 0.000 description 4
- 239000011734 sodium Substances 0.000 description 4
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- 150000003871 sulfonates Chemical class 0.000 description 4
- 238000010998 test method Methods 0.000 description 4
- 229920001567 vinyl ester resin Polymers 0.000 description 4
- VPTUPAVOBUEXMZ-UHFFFAOYSA-N (1-hydroxy-2-phosphonoethyl)phosphonic acid Chemical compound OP(=O)(O)C(O)CP(O)(O)=O VPTUPAVOBUEXMZ-UHFFFAOYSA-N 0.000 description 3
- OSSNTDFYBPYIEC-UHFFFAOYSA-N 1-ethenylimidazole Chemical compound C=CN1C=CN=C1 OSSNTDFYBPYIEC-UHFFFAOYSA-N 0.000 description 3
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- ZLMJMSJWJFRBEC-UHFFFAOYSA-N Potassium Chemical compound [K] ZLMJMSJWJFRBEC-UHFFFAOYSA-N 0.000 description 3
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- 125000002887 hydroxy group Chemical group [H]O* 0.000 description 3
- RAXXELZNTBOGNW-UHFFFAOYSA-N imidazole Natural products C1=CNC=N1 RAXXELZNTBOGNW-UHFFFAOYSA-N 0.000 description 3
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- 125000004433 nitrogen atom Chemical group N* 0.000 description 3
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- WTARULDDTDQWMU-RKDXNWHRSA-N (+)-β-pinene Chemical compound C1[C@H]2C(C)(C)[C@@H]1CCC2=C WTARULDDTDQWMU-RKDXNWHRSA-N 0.000 description 2
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- XNCSCQSQSGDGES-UHFFFAOYSA-N 2-[2-[bis(carboxymethyl)amino]propyl-(carboxymethyl)amino]acetic acid Chemical compound OC(=O)CN(CC(O)=O)C(C)CN(CC(O)=O)CC(O)=O XNCSCQSQSGDGES-UHFFFAOYSA-N 0.000 description 2
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- NKVJCKOMRJVZLO-UHFFFAOYSA-N 3,6,7-trioxabicyclo[7.2.2]trideca-1(11),9,12-triene-2,8-dione Chemical compound O=C1OCCOOC(=O)C2=CC=C1C=C2 NKVJCKOMRJVZLO-UHFFFAOYSA-N 0.000 description 2
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- PMPJQLCPEQFEJW-GNTLFSRWSA-L disodium;2-[(z)-2-[4-[4-[(z)-2-(2-sulfonatophenyl)ethenyl]phenyl]phenyl]ethenyl]benzenesulfonate Chemical compound [Na+].[Na+].[O-]S(=O)(=O)C1=CC=CC=C1\C=C/C1=CC=C(C=2C=CC(\C=C/C=3C(=CC=CC=3)S([O-])(=O)=O)=CC=2)C=C1 PMPJQLCPEQFEJW-GNTLFSRWSA-L 0.000 description 1
- YJHDFAAFYNRKQE-YHPRVSEPSA-L disodium;5-[[4-anilino-6-[bis(2-hydroxyethyl)amino]-1,3,5-triazin-2-yl]amino]-2-[(e)-2-[4-[[4-anilino-6-[bis(2-hydroxyethyl)amino]-1,3,5-triazin-2-yl]amino]-2-sulfonatophenyl]ethenyl]benzenesulfonate Chemical compound [Na+].[Na+].N=1C(NC=2C=C(C(\C=C\C=3C(=CC(NC=4N=C(N=C(NC=5C=CC=CC=5)N=4)N(CCO)CCO)=CC=3)S([O-])(=O)=O)=CC=2)S([O-])(=O)=O)=NC(N(CCO)CCO)=NC=1NC1=CC=CC=C1 YJHDFAAFYNRKQE-YHPRVSEPSA-L 0.000 description 1
- 238000004090 dissolution Methods 0.000 description 1
- 238000009826 distribution Methods 0.000 description 1
- BRDYCNFHFWUBCZ-UHFFFAOYSA-N dodecaneperoxoic acid Chemical compound CCCCCCCCCCCC(=O)OO BRDYCNFHFWUBCZ-UHFFFAOYSA-N 0.000 description 1
- 238000001035 drying Methods 0.000 description 1
- 239000003995 emulsifying agent Substances 0.000 description 1
- 239000006081 fluorescent whitening agent Substances 0.000 description 1
- 239000003574 free electron Substances 0.000 description 1
- 125000000524 functional group Chemical group 0.000 description 1
- 229930182830 galactose Natural products 0.000 description 1
- 239000008103 glucose Substances 0.000 description 1
- 229920000578 graft copolymer Polymers 0.000 description 1
- 150000004820 halides Chemical class 0.000 description 1
- 229920001519 homopolymer Polymers 0.000 description 1
- 150000002430 hydrocarbons Chemical class 0.000 description 1
- 230000007062 hydrolysis Effects 0.000 description 1
- 238000006460 hydrolysis reaction Methods 0.000 description 1
- 229920013821 hydroxy alkyl cellulose Polymers 0.000 description 1
- WGCNASOHLSPBMP-UHFFFAOYSA-N hydroxyacetaldehyde Natural products OCC=O WGCNASOHLSPBMP-UHFFFAOYSA-N 0.000 description 1
- 150000003949 imides Chemical class 0.000 description 1
- 230000001771 impaired effect Effects 0.000 description 1
- 230000006872 improvement Effects 0.000 description 1
- 238000010348 incorporation Methods 0.000 description 1
- 230000002401 inhibitory effect Effects 0.000 description 1
- 239000002563 ionic surfactant Substances 0.000 description 1
- 125000001449 isopropyl group Chemical group [H]C([H])([H])C([H])(*)C([H])([H])[H] 0.000 description 1
- 239000008101 lactose Substances 0.000 description 1
- 238000004900 laundering Methods 0.000 description 1
- 238000010412 laundry washing Methods 0.000 description 1
- 229940087305 limonene Drugs 0.000 description 1
- 150000002628 limonene derivativess Chemical class 0.000 description 1
- 229910052749 magnesium Inorganic materials 0.000 description 1
- 239000011777 magnesium Substances 0.000 description 1
- 159000000003 magnesium salts Chemical class 0.000 description 1
- 239000001630 malic acid Substances 0.000 description 1
- 235000011090 malic acid Nutrition 0.000 description 1
- 239000008268 mayonnaise Substances 0.000 description 1
- 235000010746 mayonnaise Nutrition 0.000 description 1
- 230000007246 mechanism Effects 0.000 description 1
- 229940050176 methyl chloride Drugs 0.000 description 1
- JZMJDSHXVKJFKW-UHFFFAOYSA-M methyl sulfate(1-) Chemical compound COS([O-])(=O)=O JZMJDSHXVKJFKW-UHFFFAOYSA-M 0.000 description 1
- POULHZVOKOAJMA-UHFFFAOYSA-N methyl undecanoic acid Natural products CCCCCCCCCCCC(O)=O POULHZVOKOAJMA-UHFFFAOYSA-N 0.000 description 1
- 239000002480 mineral oil Substances 0.000 description 1
- 235000010446 mineral oil Nutrition 0.000 description 1
- 238000002156 mixing Methods 0.000 description 1
- 125000002950 monocyclic group Chemical group 0.000 description 1
- 230000003472 neutralizing effect Effects 0.000 description 1
- 229920001778 nylon Polymers 0.000 description 1
- JRZJOMJEPLMPRA-UHFFFAOYSA-N olefin Natural products CCCCCCCC=C JRZJOMJEPLMPRA-UHFFFAOYSA-N 0.000 description 1
- ZQPPMHVWECSIRJ-KTKRTIGZSA-N oleic acid group Chemical group C(CCCCCCC\C=C/CCCCCCCC)(=O)O ZQPPMHVWECSIRJ-KTKRTIGZSA-N 0.000 description 1
- 239000003605 opacifier Substances 0.000 description 1
- 150000001451 organic peroxides Chemical class 0.000 description 1
- 230000003647 oxidation Effects 0.000 description 1
- IPCSVZSSVZVIGE-UHFFFAOYSA-N palmitic acid group Chemical group C(CCCCCCCCCCCCCCC)(=O)O IPCSVZSSVZVIGE-UHFFFAOYSA-N 0.000 description 1
- 239000012188 paraffin wax Substances 0.000 description 1
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- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 description 1
- WVDDGKGOMKODPV-ZQBYOMGUSA-N phenyl(114C)methanol Chemical compound O[14CH2]C1=CC=CC=C1 WVDDGKGOMKODPV-ZQBYOMGUSA-N 0.000 description 1
- 125000000843 phenylene group Chemical group C1(=C(C=CC=C1)*)* 0.000 description 1
- 235000021317 phosphate Nutrition 0.000 description 1
- UEZVMMHDMIWARA-UHFFFAOYSA-M phosphonate Chemical compound [O-]P(=O)=O UEZVMMHDMIWARA-UHFFFAOYSA-M 0.000 description 1
- 150000003009 phosphonic acids Chemical class 0.000 description 1
- PTMHPRAIXMAOOB-UHFFFAOYSA-L phosphoramidate Chemical compound NP([O-])([O-])=O PTMHPRAIXMAOOB-UHFFFAOYSA-L 0.000 description 1
- PTMHPRAIXMAOOB-UHFFFAOYSA-N phosphoramidic acid Chemical class NP(O)(O)=O PTMHPRAIXMAOOB-UHFFFAOYSA-N 0.000 description 1
- 150000004885 piperazines Chemical class 0.000 description 1
- 229920000233 poly(alkylene oxides) Polymers 0.000 description 1
- 230000000379 polymerizing effect Effects 0.000 description 1
- 229920001155 polypropylene Polymers 0.000 description 1
- 229920001451 polypropylene glycol Polymers 0.000 description 1
- 239000000843 powder Substances 0.000 description 1
- 150000003141 primary amines Chemical class 0.000 description 1
- 239000000047 product Substances 0.000 description 1
- 230000002035 prolonged effect Effects 0.000 description 1
- BDERNNFJNOPAEC-UHFFFAOYSA-N propan-1-ol Chemical compound CCCO BDERNNFJNOPAEC-UHFFFAOYSA-N 0.000 description 1
- ULWHHBHJGPPBCO-UHFFFAOYSA-N propane-1,1-diol Chemical compound CCC(O)O ULWHHBHJGPPBCO-UHFFFAOYSA-N 0.000 description 1
- ARXJGSRGQADJSQ-UHFFFAOYSA-N propylene glycol methyl ether Substances COCC(C)O ARXJGSRGQADJSQ-UHFFFAOYSA-N 0.000 description 1
- DNXIASIHZYFFRO-UHFFFAOYSA-N pyrazoline Chemical compound C1CN=NC1 DNXIASIHZYFFRO-UHFFFAOYSA-N 0.000 description 1
- UMJSCPRVCHMLSP-UHFFFAOYSA-N pyridine Natural products COC1=CC=CN=C1 UMJSCPRVCHMLSP-UHFFFAOYSA-N 0.000 description 1
- 238000005956 quaternization reaction Methods 0.000 description 1
- 238000011160 research Methods 0.000 description 1
- 238000000518 rheometry Methods 0.000 description 1
- 150000003335 secondary amines Chemical class 0.000 description 1
- 150000004760 silicates Chemical class 0.000 description 1
- 239000000344 soap Substances 0.000 description 1
- 235000010267 sodium hydrogen sulphite Nutrition 0.000 description 1
- ZUFONQSOSYEWCN-UHFFFAOYSA-M sodium;2-(methylamino)acetate Chemical compound [Na+].CNCC([O-])=O ZUFONQSOSYEWCN-UHFFFAOYSA-M 0.000 description 1
- KSAVQLQVUXSOCR-UHFFFAOYSA-N sodium;2-[dodecanoyl(methyl)amino]acetic acid Chemical compound [Na+].CCCCCCCCCCCC(=O)N(C)CC(O)=O KSAVQLQVUXSOCR-UHFFFAOYSA-N 0.000 description 1
- 239000011877 solvent mixture Substances 0.000 description 1
- 238000001179 sorption measurement Methods 0.000 description 1
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- PJANXHGTPQOBST-UHFFFAOYSA-N stilbene Chemical class C=1C=CC=CC=1C=CC1=CC=CC=C1 PJANXHGTPQOBST-UHFFFAOYSA-N 0.000 description 1
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- 235000021286 stilbenes Nutrition 0.000 description 1
- 125000005504 styryl group Chemical group 0.000 description 1
- 125000001424 substituent group Chemical group 0.000 description 1
- 125000000547 substituted alkyl group Chemical group 0.000 description 1
- 125000003107 substituted aryl group Chemical group 0.000 description 1
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- 230000001502 supplementing effect Effects 0.000 description 1
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- 239000003760 tallow Substances 0.000 description 1
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- 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 1
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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
-
- 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
- C11D3/3703—Macromolecular compounds obtained otherwise than by reactions only involving carbon-to-carbon unsaturated bonds
- C11D3/3723—Polyamines or polyalkyleneimines
-
- 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
- C11D1/38—Cationic compounds
- C11D1/42—Amino alcohols or amino ethers
- C11D1/44—Ethers of polyoxyalkylenes with amino alcohols; Condensation products of epoxyalkanes with amines
-
- 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
- C11D3/39—Organic or inorganic per-compounds
- C11D3/3947—Liquid compositions
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)
- Silver Salt Photography Or Processing Solution Therefor (AREA)
- Treatments For Attaching Organic Compounds To Fibrous Goods (AREA)
- Chemical Or Physical Treatment Of Fibers (AREA)
Applications Claiming Priority (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| EP96870137A EP0839903B1 (en) | 1996-10-31 | 1996-10-31 | Liquid aqueous bleaching compositions and pretreatment process |
| PCT/US1997/020154 WO1998018893A1 (en) | 1996-10-31 | 1997-10-30 | Liquid aqueous bleaching compositions and pretreatment process |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| SK58599A3 true SK58599A3 (en) | 2000-03-13 |
Family
ID=8226174
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| SK585-99A SK58599A3 (en) | 1996-10-31 | 1997-10-30 | Liquid aqueous bleaching compositions and pretreatment process |
Country Status (17)
| Country | Link |
|---|---|
| EP (1) | EP0839903B1 (enExample) |
| JP (1) | JP2001503460A (enExample) |
| KR (1) | KR20000052942A (enExample) |
| AT (1) | ATE229565T1 (enExample) |
| AU (1) | AU5168698A (enExample) |
| BR (1) | BR9713493A (enExample) |
| CA (1) | CA2270717A1 (enExample) |
| DE (1) | DE69625362T2 (enExample) |
| ES (1) | ES2183929T3 (enExample) |
| HU (1) | HUP0202668A2 (enExample) |
| IL (1) | IL129643A0 (enExample) |
| NO (1) | NO992034L (enExample) |
| NZ (1) | NZ335441A (enExample) |
| PL (1) | PL333230A1 (enExample) |
| SK (1) | SK58599A3 (enExample) |
| TR (1) | TR199901616T2 (enExample) |
| WO (1) | WO1998018893A1 (enExample) |
Families Citing this family (24)
| Publication number | Priority date | Publication date | Assignee | Title |
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| ATE246725T1 (de) * | 1998-02-20 | 2003-08-15 | Procter & Gamble | Bleichmittelzusammensetzungen enthaltende modifizierte polyamin-polymeren |
| EP0995792A1 (en) * | 1998-10-19 | 2000-04-26 | The Procter & Gamble Company | Process of bleaching fabrics |
| US6586382B1 (en) | 1998-10-19 | 2003-07-01 | The Procter & Gamble Company | Process of bleaching fabrics |
| ATE327309T1 (de) * | 2001-09-07 | 2006-06-15 | Procter & Gamble | Bleichmittel enthaltend ein farbstofferhaltungsmittel |
| EP1865050B1 (en) | 2006-06-08 | 2017-03-08 | The Procter & Gamble Company | Bleaching compositions |
| US12203056B2 (en) | 2008-03-28 | 2025-01-21 | Ecolab Usa Inc. | Sulfoperoxycarboxylic acids, their preparation and methods of use as bleaching and antimicrobial agents |
| MX2010010236A (es) | 2008-03-28 | 2010-10-20 | Ecolab Inc | Acidos sulfoperoxicarboxilicos, su preparacion y metodos de uso como agentes blanqueadores y antimicrobianos. |
| US8809392B2 (en) | 2008-03-28 | 2014-08-19 | Ecolab Usa Inc. | Sulfoperoxycarboxylic acids, their preparation and methods of use as bleaching and antimicrobial agents |
| US8871807B2 (en) | 2008-03-28 | 2014-10-28 | Ecolab Usa Inc. | Detergents capable of cleaning, bleaching, sanitizing and/or disinfecting textiles including sulfoperoxycarboxylic acids |
| JP5580027B2 (ja) * | 2009-12-11 | 2014-08-27 | 花王株式会社 | 液体漂白剤組成物 |
| ES2676187T3 (es) | 2010-12-29 | 2018-07-17 | Ecolab Usa Inc. | Generación de ácidos peroxcarboxílicos a pH alcalino y su uso como agentes blanqueantes textiles y antimicrobianos |
| US8846107B2 (en) | 2010-12-29 | 2014-09-30 | Ecolab Usa Inc. | In situ generation of peroxycarboxylic acids at alkaline pH, and methods of use thereof |
| US9321664B2 (en) | 2011-12-20 | 2016-04-26 | Ecolab Usa Inc. | Stable percarboxylic acid compositions and uses thereof |
| EP2831000A4 (en) | 2012-03-30 | 2016-03-30 | Ecolab Usa Inc | USE OF PERCONDIC ACID / HYDROGEN PEROXIDE AND PEROXIDE REDUCERS FOR THE TREATMENT OF DRILLING LIQUIDS, FRACKING LIQUIDS, REFILL WATER AND DISPOSAL WATER |
| US10165774B2 (en) | 2013-03-05 | 2019-01-01 | Ecolab Usa Inc. | Defoamer useful in a peracid composition with anionic surfactants |
| US8822719B1 (en) | 2013-03-05 | 2014-09-02 | Ecolab Usa Inc. | Peroxycarboxylic acid compositions suitable for inline optical or conductivity monitoring |
| US20140256811A1 (en) | 2013-03-05 | 2014-09-11 | Ecolab Usa Inc. | Efficient stabilizer in controlling self accelerated decomposition temperature of peroxycarboxylic acid compositions with mineral acids |
| US10060073B2 (en) | 2013-05-23 | 2018-08-28 | Washing Systems, Llc | Method of laundering industrial garments |
| US10519400B2 (en) | 2013-05-24 | 2019-12-31 | The Procter & Gamble Company | Low PH detergent composition |
| EP3004307A1 (en) | 2013-05-24 | 2016-04-13 | The Procter & Gamble Company | Low ph detergent composition comprising nonionic surfactants |
| JP6271717B2 (ja) | 2013-05-24 | 2018-01-31 | ザ プロクター アンド ギャンブル カンパニー | 濃縮界面活性剤組成物 |
| US10093884B2 (en) | 2016-10-14 | 2018-10-09 | The Clorox Company | Peroxide-free polymer and surfactant liquid laundry additive compositions |
| BR112021002549A2 (pt) | 2018-08-22 | 2021-05-04 | Ecolab Usa Inc. | composição de ácido peroxicarboxílico estabilizada, e, método para reduzir uma população microbiana usando uma composição de ácido peroxicarboxílico estabilizada. |
| US12096768B2 (en) | 2019-08-07 | 2024-09-24 | Ecolab Usa Inc. | Polymeric and solid-supported chelators for stabilization of peracid-containing compositions |
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| Publication number | Priority date | Publication date | Assignee | Title |
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| US1985424A (en) | 1933-03-23 | 1934-12-25 | Ici Ltd | Alkylene-oxide derivatives of polyhydroxyalkyl-alkylamides |
| US2182306A (en) | 1935-05-10 | 1939-12-05 | Ig Farbenindustrie Ag | Polymerization of ethylene imines |
| US2208095A (en) | 1937-01-05 | 1940-07-16 | Ig Farbenindustrie Ag | Process of producing insoluble condensation products containing sulphur and nitrogen |
| US2533696A (en) | 1949-09-09 | 1950-12-12 | George W Schaeffer | Diborane purification process |
| US2703798A (en) | 1950-05-25 | 1955-03-08 | Commercial Solvents Corp | Detergents from nu-monoalkyl-glucamines |
| US2806839A (en) | 1953-02-24 | 1957-09-17 | Arnold Hoffman & Co Inc | Preparation of polyimines from 2-oxazolidone |
| US2792372A (en) | 1954-09-15 | 1957-05-14 | Petrolite Corp | Process for breaking petroleum emulsions employing certain oxyalkylated higher polyethylene amines |
| BE557103A (enExample) | 1956-05-14 | |||
| BE615597A (enExample) | 1958-06-19 | |||
| GB1082179A (en) | 1965-07-19 | 1967-09-06 | Citrique Belge Nv | Unsaturated carboxylic salt materials and derivatives thereof |
| US3812044A (en) | 1970-12-28 | 1974-05-21 | Procter & Gamble | Detergent composition containing a polyfunctionally-substituted aromatic acid sequestering agent |
| CA989557A (en) | 1971-10-28 | 1976-05-25 | The Procter And Gamble Company | Compositions and process for imparting renewable soil release finish to polyester-containing fabrics |
| US3959230A (en) | 1974-06-25 | 1976-05-25 | The Procter & Gamble Company | Polyethylene oxide terephthalate polymers |
| US3929678A (en) | 1974-08-01 | 1975-12-30 | Procter & Gamble | Detergent composition having enhanced particulate soil removal performance |
| US4000093A (en) | 1975-04-02 | 1976-12-28 | The Procter & Gamble Company | Alkyl sulfate detergent compositions |
| GB1586769A (en) | 1976-10-06 | 1981-03-25 | Procter & Gamble Ltd | Laundry additive product |
| US4259201A (en) | 1979-11-09 | 1981-03-31 | The Procter & Gamble Company | Detergent composition containing organic peracids buffered for optimum performance |
| US4399049A (en) | 1981-04-08 | 1983-08-16 | The Procter & Gamble Company | Detergent additive compositions |
| EP0111984B1 (en) * | 1982-12-23 | 1989-08-02 | THE PROCTER & GAMBLE COMPANY | Ethoxylated amine polymers having clay soil removal/anti-redeposition properties useful in detergent compositions |
| US4659802A (en) | 1982-12-23 | 1987-04-21 | The Procter & Gamble Company | Cationic compounds having clay soil removal/anti-redeposition properties useful in detergent compositions |
| US4664848A (en) * | 1982-12-23 | 1987-05-12 | The Procter & Gamble Company | Detergent compositions containing cationic compounds having clay soil removal/anti-redeposition properties |
| EP0111965B1 (en) | 1982-12-23 | 1989-07-26 | THE PROCTER & GAMBLE COMPANY | Detergent compositions containing cationic compounds having clay soil removal/anti-redeposition properties |
| GB8304990D0 (en) | 1983-02-23 | 1983-03-30 | Procter & Gamble | Detergent ingredients |
| US4561991A (en) * | 1984-08-06 | 1985-12-31 | The Procter & Gamble Company | Fabric cleaning compositions for clay-based stains |
| US4790856A (en) | 1984-10-17 | 1988-12-13 | Colgate-Palmolive Company | Softening and anti-static nonionic detergent composition with sulfosuccinamate detergent |
| US4702857A (en) | 1984-12-21 | 1987-10-27 | The Procter & Gamble Company | Block polyesters and like compounds useful as soil release agents in detergent compositions |
| DE3536530A1 (de) | 1985-10-12 | 1987-04-23 | Basf Ag | Verwendung von pfropfcopolymerisaten aus polyalkylenoxiden und vinylacetat als vergrauungsinhibitoren beim waschen und nachbehandeln von synthesefasern enthaltendem textilgut |
| US4711730A (en) | 1986-04-15 | 1987-12-08 | The Procter & Gamble Company | Capped 1,2-propylene terephthalate-polyoxyethylene terephthalate polyesters useful as soil release agents |
| US4818425A (en) | 1986-05-28 | 1989-04-04 | Akzo N.V. | Process for the preparation of diperoxydodecanedioic acid-containing agglomerates and compositions in which these agglomerates are used as bleaching component |
| GB8618635D0 (en) | 1986-07-30 | 1986-09-10 | Unilever Plc | Detergent composition |
| US4954292A (en) | 1986-10-01 | 1990-09-04 | Lever Brothers Co. | Detergent composition containing PVP and process of using same |
| US4704233A (en) | 1986-11-10 | 1987-11-03 | The Procter & Gamble Company | Detergent compositions containing ethylenediamine-N,N'-disuccinic acid |
| US4770666A (en) | 1986-12-12 | 1988-09-13 | The Procter & Gamble Company | Laundry composition containing peroxyacid bleach and soil release agent |
| US4721580A (en) | 1987-01-07 | 1988-01-26 | The Procter & Gamble Company | Anionic end-capped oligomeric esters as soil release agents in detergent compositions |
| US4877896A (en) | 1987-10-05 | 1989-10-31 | The Procter & Gamble Company | Sulfoaroyl end-capped ester of oligomers suitable as soil-release agents in detergent compositions and fabric-conditioner articles |
| US4968451A (en) | 1988-08-26 | 1990-11-06 | The Procter & Gamble Company | Soil release agents having allyl-derived sulfonated end caps |
| CA2092193C (en) | 1990-09-28 | 1998-08-18 | Daniel Stedman Connor | High catalyst process for glucamide detergents |
| RU2108320C1 (ru) | 1991-12-13 | 1998-04-10 | Дзе Проктер Энд Гэмбл Компани | Активатор пероксида водорода и композиция для отбеливания или дезинфекции на его основе |
| US5415807A (en) | 1993-07-08 | 1995-05-16 | The Procter & Gamble Company | Sulfonated poly-ethoxy/propoxy end-capped ester oligomers suitable as soil release agents in detergent compositions |
| US5512699A (en) * | 1994-01-25 | 1996-04-30 | The Procter & Gamble Company | Poly polyhydroxy fatty acid amides |
| JP3330226B2 (ja) * | 1994-06-10 | 2002-09-30 | 花王株式会社 | 液体漂白剤組成物 |
| SK115597A3 (en) * | 1995-02-28 | 1998-06-03 | Procter & Gamble | Laundry pretreatment with peroxide bleaches containing chelators for iron, copper or manganese for reduced fabric damage |
-
1996
- 1996-10-31 ES ES96870137T patent/ES2183929T3/es not_active Expired - Lifetime
- 1996-10-31 EP EP96870137A patent/EP0839903B1/en not_active Expired - Lifetime
- 1996-10-31 AT AT96870137T patent/ATE229565T1/de not_active IP Right Cessation
- 1996-10-31 DE DE69625362T patent/DE69625362T2/de not_active Expired - Lifetime
-
1997
- 1997-10-30 AU AU51686/98A patent/AU5168698A/en not_active Abandoned
- 1997-10-30 PL PL97333230A patent/PL333230A1/xx unknown
- 1997-10-30 IL IL12964397A patent/IL129643A0/xx unknown
- 1997-10-30 NZ NZ335441A patent/NZ335441A/en unknown
- 1997-10-30 JP JP52082098A patent/JP2001503460A/ja not_active Withdrawn
- 1997-10-30 BR BR9713493-7A patent/BR9713493A/pt not_active Application Discontinuation
- 1997-10-30 TR TR1999/01616T patent/TR199901616T2/xx unknown
- 1997-10-30 SK SK585-99A patent/SK58599A3/sk unknown
- 1997-10-30 WO PCT/US1997/020154 patent/WO1998018893A1/en not_active Ceased
- 1997-10-30 KR KR1019990703815A patent/KR20000052942A/ko not_active Ceased
- 1997-10-30 CA CA002270717A patent/CA2270717A1/en not_active Abandoned
- 1997-10-30 HU HU0202668A patent/HUP0202668A2/hu unknown
-
1999
- 1999-04-28 NO NO992034A patent/NO992034L/no not_active Application Discontinuation
Also Published As
| Publication number | Publication date |
|---|---|
| DE69625362D1 (de) | 2003-01-23 |
| NZ335441A (en) | 2001-02-23 |
| TR199901616T2 (xx) | 1999-09-21 |
| PL333230A1 (en) | 1999-11-22 |
| ATE229565T1 (de) | 2002-12-15 |
| JP2001503460A (ja) | 2001-03-13 |
| HUP0202668A2 (hu) | 2002-11-28 |
| ES2183929T3 (es) | 2003-04-01 |
| CA2270717A1 (en) | 1998-05-07 |
| NO992034L (no) | 1999-06-30 |
| IL129643A0 (en) | 2000-02-29 |
| EP0839903A1 (en) | 1998-05-06 |
| NO992034D0 (no) | 1999-04-28 |
| AU5168698A (en) | 1998-05-22 |
| KR20000052942A (ko) | 2000-08-25 |
| WO1998018893A1 (en) | 1998-05-07 |
| BR9713493A (pt) | 2000-02-29 |
| DE69625362T2 (de) | 2003-10-30 |
| EP0839903B1 (en) | 2002-12-11 |
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