EP3020794A2 - Composition de lessive et son utilisation - Google Patents
Composition de lessive et son utilisation Download PDFInfo
- Publication number
- EP3020794A2 EP3020794A2 EP15194014.5A EP15194014A EP3020794A2 EP 3020794 A2 EP3020794 A2 EP 3020794A2 EP 15194014 A EP15194014 A EP 15194014A EP 3020794 A2 EP3020794 A2 EP 3020794A2
- Authority
- EP
- European Patent Office
- Prior art keywords
- amount
- weight
- detergent composition
- acid
- dye
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Granted
Links
- 239000000203 mixture Substances 0.000 title claims abstract description 75
- 239000003599 detergent Substances 0.000 title claims abstract description 69
- 239000000985 reactive dye Substances 0.000 claims abstract description 34
- 239000000982 direct dye Substances 0.000 claims abstract description 29
- 238000005406 washing Methods 0.000 claims abstract description 13
- 239000004753 textile Substances 0.000 claims abstract description 6
- 238000004043 dyeing Methods 0.000 claims abstract description 5
- 239000000975 dye Substances 0.000 claims description 24
- 239000010457 zeolite Substances 0.000 claims description 22
- 239000000344 soap Substances 0.000 claims description 19
- 102000004190 Enzymes Human genes 0.000 claims description 16
- 108090000790 Enzymes Proteins 0.000 claims description 16
- 239000000980 acid dye Substances 0.000 claims description 12
- AFOSIXZFDONLBT-UHFFFAOYSA-N divinyl sulfone Chemical compound C=CS(=O)(=O)C=C AFOSIXZFDONLBT-UHFFFAOYSA-N 0.000 claims description 12
- 239000004094 surface-active agent Substances 0.000 claims description 12
- 229910021536 Zeolite Inorganic materials 0.000 claims description 8
- HNPSIPDUKPIQMN-UHFFFAOYSA-N dioxosilane;oxo(oxoalumanyloxy)alumane Chemical group O=[Si]=O.O=[Al]O[Al]=O HNPSIPDUKPIQMN-UHFFFAOYSA-N 0.000 claims description 8
- HFIYIRIMGZMCPC-YOLJWEMLSA-J remazole black-GR Chemical group [Na+].[Na+].[Na+].[Na+].[O-]S(=O)(=O)C1=CC2=CC(S([O-])(=O)=O)=C(\N=N\C=3C=CC(=CC=3)S(=O)(=O)CCOS([O-])(=O)=O)C(O)=C2C(N)=C1\N=N\C1=CC=C(S(=O)(=O)CCOS([O-])(=O)=O)C=C1 HFIYIRIMGZMCPC-YOLJWEMLSA-J 0.000 claims description 6
- 159000000000 sodium salts Chemical class 0.000 claims description 6
- BPQQTUXANYXVAA-UHFFFAOYSA-N Orthosilicate Chemical group [O-][Si]([O-])([O-])[O-] BPQQTUXANYXVAA-UHFFFAOYSA-N 0.000 claims description 2
- 239000003086 colorant Substances 0.000 abstract description 8
- 206010016256 fatigue Diseases 0.000 abstract description 2
- IAYPIBMASNFSPL-UHFFFAOYSA-N Ethylene oxide Chemical compound C1CO1 IAYPIBMASNFSPL-UHFFFAOYSA-N 0.000 description 24
- 239000003945 anionic surfactant Substances 0.000 description 20
- 239000002736 nonionic surfactant Substances 0.000 description 20
- 239000002253 acid Substances 0.000 description 19
- FAPWRFPIFSIZLT-UHFFFAOYSA-M Sodium chloride Chemical compound [Na+].[Cl-] FAPWRFPIFSIZLT-UHFFFAOYSA-M 0.000 description 16
- 239000004115 Sodium Silicate Substances 0.000 description 15
- 229940088598 enzyme Drugs 0.000 description 15
- 125000000129 anionic group Chemical group 0.000 description 14
- 235000014113 dietary fatty acids Nutrition 0.000 description 14
- 239000000194 fatty acid Substances 0.000 description 14
- 229930195729 fatty acid Natural products 0.000 description 14
- 150000007513 acids Chemical class 0.000 description 12
- 150000002191 fatty alcohols Chemical class 0.000 description 12
- 235000019795 sodium metasilicate Nutrition 0.000 description 12
- NTHWMYGWWRZVTN-UHFFFAOYSA-N sodium silicate Chemical compound [Na+].[Na+].[O-][Si]([O-])=O NTHWMYGWWRZVTN-UHFFFAOYSA-N 0.000 description 12
- 229910052911 sodium silicate Inorganic materials 0.000 description 12
- 150000001298 alcohols Chemical class 0.000 description 11
- 239000003205 fragrance Substances 0.000 description 11
- 125000004432 carbon atom Chemical group C* 0.000 description 10
- -1 hydroxide anions Chemical class 0.000 description 10
- 239000003921 oil Substances 0.000 description 10
- 235000019198 oils Nutrition 0.000 description 10
- 150000003839 salts Chemical class 0.000 description 10
- KRKNYBCHXYNGOX-UHFFFAOYSA-N citric acid Chemical compound OC(=O)CC(O)(C(O)=O)CC(O)=O KRKNYBCHXYNGOX-UHFFFAOYSA-N 0.000 description 9
- 150000004665 fatty acids Chemical class 0.000 description 9
- 239000000835 fiber Substances 0.000 description 9
- CDBYLPFSWZWCQE-UHFFFAOYSA-L Sodium Carbonate Chemical compound [Na+].[Na+].[O-]C([O-])=O CDBYLPFSWZWCQE-UHFFFAOYSA-L 0.000 description 8
- 125000002887 hydroxy group Chemical group [H]O* 0.000 description 8
- 239000011734 sodium Substances 0.000 description 8
- 239000011780 sodium chloride Substances 0.000 description 8
- 150000004760 silicates Chemical class 0.000 description 7
- 239000000126 substance Substances 0.000 description 7
- 229920002245 Dextrose equivalent Polymers 0.000 description 6
- WNLRTRBMVRJNCN-UHFFFAOYSA-N adipic acid Chemical compound OC(=O)CCCCC(O)=O WNLRTRBMVRJNCN-UHFFFAOYSA-N 0.000 description 6
- 150000001875 compounds Chemical class 0.000 description 6
- 239000000047 product Substances 0.000 description 6
- 229910052708 sodium Inorganic materials 0.000 description 6
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 5
- 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 5
- 102000035195 Peptidases Human genes 0.000 description 5
- 108091005804 Peptidases Proteins 0.000 description 5
- 239000004365 Protease Substances 0.000 description 5
- PMZURENOXWZQFD-UHFFFAOYSA-L Sodium Sulfate Chemical compound [Na+].[Na+].[O-]S([O-])(=O)=O PMZURENOXWZQFD-UHFFFAOYSA-L 0.000 description 5
- ULUAUXLGCMPNKK-UHFFFAOYSA-N Sulfobutanedioic acid Chemical class OC(=O)CC(C(O)=O)S(O)(=O)=O ULUAUXLGCMPNKK-UHFFFAOYSA-N 0.000 description 5
- 238000003776 cleavage reaction Methods 0.000 description 5
- 239000012038 nucleophile Substances 0.000 description 5
- 230000000269 nucleophilic effect Effects 0.000 description 5
- 239000002304 perfume Substances 0.000 description 5
- 230000007017 scission Effects 0.000 description 5
- 229910052938 sodium sulfate Inorganic materials 0.000 description 5
- 235000011152 sodium sulphate Nutrition 0.000 description 5
- 239000003760 tallow Substances 0.000 description 5
- VZCYOOQTPOCHFL-UHFFFAOYSA-N trans-butenedioic acid Natural products OC(=O)C=CC(O)=O VZCYOOQTPOCHFL-UHFFFAOYSA-N 0.000 description 5
- SMZOUWXMTYCWNB-UHFFFAOYSA-N 2-(2-methoxy-5-methylphenyl)ethanamine Chemical compound COC1=CC=C(C)C=C1CCN SMZOUWXMTYCWNB-UHFFFAOYSA-N 0.000 description 4
- NIXOWILDQLNWCW-UHFFFAOYSA-N 2-Propenoic acid Natural products OC(=O)C=C NIXOWILDQLNWCW-UHFFFAOYSA-N 0.000 description 4
- 244000060011 Cocos nucifera Species 0.000 description 4
- 235000013162 Cocos nucifera Nutrition 0.000 description 4
- 229920000742 Cotton Polymers 0.000 description 4
- RGHNJXZEOKUKBD-SQOUGZDYSA-N D-gluconic acid Chemical compound OC[C@@H](O)[C@@H](O)[C@H](O)[C@@H](O)C(O)=O RGHNJXZEOKUKBD-SQOUGZDYSA-N 0.000 description 4
- OFOBLEOULBTSOW-UHFFFAOYSA-N Propanedioic acid Natural products OC(=O)CC(O)=O OFOBLEOULBTSOW-UHFFFAOYSA-N 0.000 description 4
- 239000002738 chelating agent Substances 0.000 description 4
- UKMSUNONTOPOIO-UHFFFAOYSA-N docosanoic acid Chemical compound CCCCCCCCCCCCCCCCCCCCCC(O)=O UKMSUNONTOPOIO-UHFFFAOYSA-N 0.000 description 4
- POULHZVOKOAJMA-UHFFFAOYSA-N dodecanoic acid Chemical compound CCCCCCCCCCCC(O)=O POULHZVOKOAJMA-UHFFFAOYSA-N 0.000 description 4
- 150000002148 esters Chemical class 0.000 description 4
- 238000002474 experimental method Methods 0.000 description 4
- IPCSVZSSVZVIGE-UHFFFAOYSA-N hexadecanoic acid Chemical compound CCCCCCCCCCCCCCCC(O)=O IPCSVZSSVZVIGE-UHFFFAOYSA-N 0.000 description 4
- 230000007062 hydrolysis Effects 0.000 description 4
- 238000006460 hydrolysis reaction Methods 0.000 description 4
- VZCYOOQTPOCHFL-UPHRSURJSA-N maleic acid Chemical compound OC(=O)\C=C/C(O)=O VZCYOOQTPOCHFL-UPHRSURJSA-N 0.000 description 4
- 239000011976 maleic acid Substances 0.000 description 4
- 238000000034 method Methods 0.000 description 4
- 229920005646 polycarboxylate Polymers 0.000 description 4
- 229920000642 polymer Polymers 0.000 description 4
- 229910000029 sodium carbonate Inorganic materials 0.000 description 4
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 4
- RTBFRGCFXZNCOE-UHFFFAOYSA-N 1-methylsulfonylpiperidin-4-one Chemical compound CS(=O)(=O)N1CCC(=O)CC1 RTBFRGCFXZNCOE-UHFFFAOYSA-N 0.000 description 3
- 229920001353 Dextrin Polymers 0.000 description 3
- 239000004375 Dextrin Substances 0.000 description 3
- WQZGKKKJIJFFOK-GASJEMHNSA-N Glucose Natural products OC[C@H]1OC(O)[C@H](O)[C@@H](O)[C@@H]1O WQZGKKKJIJFFOK-GASJEMHNSA-N 0.000 description 3
- PEDCQBHIVMGVHV-UHFFFAOYSA-N Glycerine Chemical compound OCC(O)CO PEDCQBHIVMGVHV-UHFFFAOYSA-N 0.000 description 3
- SJEYSFABYSGQBG-UHFFFAOYSA-M Patent blue Chemical compound [Na+].C1=CC(N(CC)CC)=CC=C1C(C=1C(=CC(=CC=1)S([O-])(=O)=O)S([O-])(=O)=O)=C1C=CC(=[N+](CC)CC)C=C1 SJEYSFABYSGQBG-UHFFFAOYSA-M 0.000 description 3
- KDYFGRWQOYBRFD-UHFFFAOYSA-N Succinic acid Natural products OC(=O)CCC(O)=O KDYFGRWQOYBRFD-UHFFFAOYSA-N 0.000 description 3
- 239000001361 adipic acid Substances 0.000 description 3
- 235000011037 adipic acid Nutrition 0.000 description 3
- 150000008051 alkyl sulfates Chemical class 0.000 description 3
- JFCQEDHGNNZCLN-UHFFFAOYSA-N anhydrous glutaric acid Natural products OC(=O)CCCC(O)=O JFCQEDHGNNZCLN-UHFFFAOYSA-N 0.000 description 3
- 239000007864 aqueous solution Substances 0.000 description 3
- KDYFGRWQOYBRFD-NUQCWPJISA-N butanedioic acid Chemical compound O[14C](=O)CC[14C](O)=O KDYFGRWQOYBRFD-NUQCWPJISA-N 0.000 description 3
- 229920001577 copolymer Polymers 0.000 description 3
- 235000019425 dextrin Nutrition 0.000 description 3
- 238000009826 distribution Methods 0.000 description 3
- 150000002576 ketones Chemical class 0.000 description 3
- 230000008569 process Effects 0.000 description 3
- 235000019351 sodium silicates Nutrition 0.000 description 3
- WRMNZCZEMHIOCP-UHFFFAOYSA-N 2-phenylethanol Chemical compound OCCC1=CC=CC=C1 WRMNZCZEMHIOCP-UHFFFAOYSA-N 0.000 description 2
- 235000021357 Behenic acid Nutrition 0.000 description 2
- ZCTQGTTXIYCGGC-UHFFFAOYSA-N Benzyl salicylate Chemical compound OC1=CC=CC=C1C(=O)OCC1=CC=CC=C1 ZCTQGTTXIYCGGC-UHFFFAOYSA-N 0.000 description 2
- UYWQUFXKFGHYNT-UHFFFAOYSA-N Benzylformate Chemical compound O=COCC1=CC=CC=C1 UYWQUFXKFGHYNT-UHFFFAOYSA-N 0.000 description 2
- RGHNJXZEOKUKBD-UHFFFAOYSA-N D-gluconic acid Natural products OCC(O)C(O)C(O)C(O)C(O)=O RGHNJXZEOKUKBD-UHFFFAOYSA-N 0.000 description 2
- FEWJPZIEWOKRBE-JCYAYHJZSA-N Dextrotartaric acid Chemical compound OC(=O)[C@H](O)[C@@H](O)C(O)=O FEWJPZIEWOKRBE-JCYAYHJZSA-N 0.000 description 2
- RTZKZFJDLAIYFH-UHFFFAOYSA-N Diethyl ether Chemical compound CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 description 2
- VZCYOOQTPOCHFL-OWOJBTEDSA-N Fumaric acid Chemical compound OC(=O)\C=C\C(O)=O VZCYOOQTPOCHFL-OWOJBTEDSA-N 0.000 description 2
- GLZPCOQZEFWAFX-UHFFFAOYSA-N Geraniol Chemical compound CC(C)=CCCC(C)=CCO GLZPCOQZEFWAFX-UHFFFAOYSA-N 0.000 description 2
- 239000005639 Lauric acid Substances 0.000 description 2
- BTJXBZZBBNNTOV-UHFFFAOYSA-N Linalyl benzoate Chemical compound CC(C)=CCCC(C)(C=C)OC(=O)C1=CC=CC=C1 BTJXBZZBBNNTOV-UHFFFAOYSA-N 0.000 description 2
- CERQOIWHTDAKMF-UHFFFAOYSA-N Methacrylic acid Chemical compound CC(=C)C(O)=O CERQOIWHTDAKMF-UHFFFAOYSA-N 0.000 description 2
- 229910019142 PO4 Inorganic materials 0.000 description 2
- 235000021314 Palmitic acid Nutrition 0.000 description 2
- 229910004298 SiO 2 Inorganic materials 0.000 description 2
- 229920002125 Sokalan® Polymers 0.000 description 2
- 235000021355 Stearic acid Nutrition 0.000 description 2
- FEWJPZIEWOKRBE-UHFFFAOYSA-N Tartaric acid Natural products [H+].[H+].[O-]C(=O)C(O)C(O)C([O-])=O FEWJPZIEWOKRBE-UHFFFAOYSA-N 0.000 description 2
- 150000001299 aldehydes Chemical class 0.000 description 2
- 229910052783 alkali metal Inorganic materials 0.000 description 2
- 125000000217 alkyl group Chemical group 0.000 description 2
- 230000002152 alkylating effect Effects 0.000 description 2
- 150000001450 anions Chemical class 0.000 description 2
- 229940116226 behenic acid Drugs 0.000 description 2
- QUKGYYKBILRGFE-UHFFFAOYSA-N benzyl acetate Chemical compound CC(=O)OCC1=CC=CC=C1 QUKGYYKBILRGFE-UHFFFAOYSA-N 0.000 description 2
- 150000004649 carbonic acid derivatives Chemical class 0.000 description 2
- 229920002678 cellulose Polymers 0.000 description 2
- 239000001913 cellulose Substances 0.000 description 2
- 238000006243 chemical reaction Methods 0.000 description 2
- NEHNMFOYXAPHSD-UHFFFAOYSA-N citronellal Chemical compound O=CCC(C)CCC=C(C)C NEHNMFOYXAPHSD-UHFFFAOYSA-N 0.000 description 2
- QMVPMAAFGQKVCJ-UHFFFAOYSA-N citronellol Chemical compound OCCC(C)CCC=C(C)C QMVPMAAFGQKVCJ-UHFFFAOYSA-N 0.000 description 2
- 239000012459 cleaning agent Substances 0.000 description 2
- 239000000356 contaminant Substances 0.000 description 2
- GHVNFZFCNZKVNT-UHFFFAOYSA-N decanoic acid Chemical compound CCCCCCCCCC(O)=O GHVNFZFCNZKVNT-UHFFFAOYSA-N 0.000 description 2
- 150000005690 diesters Chemical class 0.000 description 2
- RRAFCDWBNXTKKO-UHFFFAOYSA-N eugenol Chemical compound COC1=CC(CC=C)=CC=C1O RRAFCDWBNXTKKO-UHFFFAOYSA-N 0.000 description 2
- 238000005227 gel permeation chromatography Methods 0.000 description 2
- 239000000174 gluconic acid Substances 0.000 description 2
- 235000012208 gluconic acid Nutrition 0.000 description 2
- 239000008103 glucose Substances 0.000 description 2
- 150000004676 glycans Chemical class 0.000 description 2
- LEQAOMBKQFMDFZ-UHFFFAOYSA-N glyoxal Chemical compound O=CC=O LEQAOMBKQFMDFZ-UHFFFAOYSA-N 0.000 description 2
- FUZZWVXGSFPDMH-UHFFFAOYSA-N hexanoic acid Chemical compound CCCCCC(O)=O FUZZWVXGSFPDMH-UHFFFAOYSA-N 0.000 description 2
- 229930195733 hydrocarbon Natural products 0.000 description 2
- 150000002430 hydrocarbons Chemical class 0.000 description 2
- 230000003993 interaction Effects 0.000 description 2
- XMGQYMWWDOXHJM-UHFFFAOYSA-N limonene Chemical compound CC(=C)C1CCC(C)=CC1 XMGQYMWWDOXHJM-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
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 description 2
- 239000000178 monomer Substances 0.000 description 2
- WQEPLUUGTLDZJY-UHFFFAOYSA-N n-Pentadecanoic acid Natural products CCCCCCCCCCCCCCC(O)=O WQEPLUUGTLDZJY-UHFFFAOYSA-N 0.000 description 2
- GLDOVTGHNKAZLK-UHFFFAOYSA-N octadecan-1-ol Chemical compound CCCCCCCCCCCCCCCCCCO GLDOVTGHNKAZLK-UHFFFAOYSA-N 0.000 description 2
- QIQXTHQIDYTFRH-UHFFFAOYSA-N octadecanoic acid Chemical compound CCCCCCCCCCCCCCCCCC(O)=O QIQXTHQIDYTFRH-UHFFFAOYSA-N 0.000 description 2
- OQCDKBAXFALNLD-UHFFFAOYSA-N octadecanoic acid Natural products CCCCCCCC(C)CCCCCCCCC(O)=O OQCDKBAXFALNLD-UHFFFAOYSA-N 0.000 description 2
- WWZKQHOCKIZLMA-UHFFFAOYSA-N octanoic acid Chemical compound CCCCCCCC(O)=O WWZKQHOCKIZLMA-UHFFFAOYSA-N 0.000 description 2
- 239000002245 particle Substances 0.000 description 2
- MDHYEMXUFSJLGV-UHFFFAOYSA-N phenethyl acetate Chemical compound CC(=O)OCCC1=CC=CC=C1 MDHYEMXUFSJLGV-UHFFFAOYSA-N 0.000 description 2
- 235000021317 phosphate Nutrition 0.000 description 2
- 150000003013 phosphoric acid derivatives Chemical class 0.000 description 2
- 229920000058 polyacrylate Polymers 0.000 description 2
- 239000004584 polyacrylic acid Substances 0.000 description 2
- 229920006324 polyoxymethylene Polymers 0.000 description 2
- 229920001282 polysaccharide Polymers 0.000 description 2
- 239000005017 polysaccharide Substances 0.000 description 2
- 239000000843 powder Substances 0.000 description 2
- 238000002360 preparation method Methods 0.000 description 2
- 230000009257 reactivity Effects 0.000 description 2
- GHMLBKRAJCXXBS-UHFFFAOYSA-N resorcinol Chemical compound OC1=CC=CC(O)=C1 GHMLBKRAJCXXBS-UHFFFAOYSA-N 0.000 description 2
- 150000004671 saturated fatty acids Chemical class 0.000 description 2
- 238000007086 side reaction Methods 0.000 description 2
- 239000008117 stearic acid Substances 0.000 description 2
- 235000000346 sugar Nutrition 0.000 description 2
- BDHFUVZGWQCTTF-UHFFFAOYSA-M sulfonate Chemical compound [O-]S(=O)=O BDHFUVZGWQCTTF-UHFFFAOYSA-M 0.000 description 2
- AKEJUJNQAAGONA-UHFFFAOYSA-N sulfur trioxide Chemical compound O=S(=O)=O AKEJUJNQAAGONA-UHFFFAOYSA-N 0.000 description 2
- 239000011975 tartaric acid Substances 0.000 description 2
- 235000002906 tartaric acid Nutrition 0.000 description 2
- TUNFSRHWOTWDNC-HKGQFRNVSA-N tetradecanoic acid Chemical compound CCCCCCCCCCCCC[14C](O)=O TUNFSRHWOTWDNC-HKGQFRNVSA-N 0.000 description 2
- RUVINXPYWBROJD-ONEGZZNKSA-N trans-anethole Chemical compound COC1=CC=C(\C=C\C)C=C1 RUVINXPYWBROJD-ONEGZZNKSA-N 0.000 description 2
- 239000001490 (3R)-3,7-dimethylocta-1,6-dien-3-ol Substances 0.000 description 1
- ALSTYHKOOCGGFT-KTKRTIGZSA-N (9Z)-octadecen-1-ol Chemical compound CCCCCCCC\C=C/CCCCCCCCO ALSTYHKOOCGGFT-KTKRTIGZSA-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
- BJEPYKJPYRNKOW-REOHCLBHSA-N (S)-malic acid Chemical compound OC(=O)[C@@H](O)CC(O)=O BJEPYKJPYRNKOW-REOHCLBHSA-N 0.000 description 1
- YYMCVDNIIFNDJK-XFQWXJFMSA-N (z)-1-(3-fluorophenyl)-n-[(z)-(3-fluorophenyl)methylideneamino]methanimine Chemical compound FC1=CC=CC(\C=N/N=C\C=2C=C(F)C=CC=2)=C1 YYMCVDNIIFNDJK-XFQWXJFMSA-N 0.000 description 1
- JYEUMXHLPRZUAT-UHFFFAOYSA-N 1,2,3-triazine Chemical compound C1=CN=NN=C1 JYEUMXHLPRZUAT-UHFFFAOYSA-N 0.000 description 1
- WCIQNYOXLZQQMU-UHFFFAOYSA-N 1-Phenylethyl propanoate Chemical compound CCC(=O)OC(C)C1=CC=CC=C1 WCIQNYOXLZQQMU-UHFFFAOYSA-N 0.000 description 1
- HLZKNKRTKFSKGZ-UHFFFAOYSA-N 1-Tetradecanol Natural products CCCCCCCCCCCCCCO HLZKNKRTKFSKGZ-UHFFFAOYSA-N 0.000 description 1
- MPJQXAIKMSKXBI-UHFFFAOYSA-N 2,7,9,14-tetraoxa-1,8-diazabicyclo[6.6.2]hexadecane-3,6,10,13-tetrone Chemical compound C1CN2OC(=O)CCC(=O)ON1OC(=O)CCC(=O)O2 MPJQXAIKMSKXBI-UHFFFAOYSA-N 0.000 description 1
- CFPOJWPDQWJEMO-UHFFFAOYSA-N 2-(1,2-dicarboxyethoxy)butanedioic acid Chemical class OC(=O)CC(C(O)=O)OC(C(O)=O)CC(O)=O CFPOJWPDQWJEMO-UHFFFAOYSA-N 0.000 description 1
- FLUWAIIVLCVEKF-UHFFFAOYSA-N 2-Methyl-1-phenyl-2-propanyl acetate Chemical compound CC(=O)OC(C)(C)CC1=CC=CC=C1 FLUWAIIVLCVEKF-UHFFFAOYSA-N 0.000 description 1
- MJTPMXWJHPOWGH-UHFFFAOYSA-N 2-Phenoxyethyl isobutyrate Chemical compound CC(C)C(=O)OCCOC1=CC=CC=C1 MJTPMXWJHPOWGH-UHFFFAOYSA-N 0.000 description 1
- ZJVJPPNOQCMEPI-UHFFFAOYSA-N 2-[ethyl(methyl)amino]-2-phenylacetic acid Chemical compound CCN(C)C(C(O)=O)C1=CC=CC=C1 ZJVJPPNOQCMEPI-UHFFFAOYSA-N 0.000 description 1
- XEEYSDHEOQHCDA-UHFFFAOYSA-N 2-methylprop-2-ene-1-sulfonic acid Chemical compound CC(=C)CS(O)(=O)=O XEEYSDHEOQHCDA-UHFFFAOYSA-N 0.000 description 1
- JRJBVWJSTHECJK-PKNBQFBNSA-N 3-Methyl-4-(2,6,6-trimethyl-2-cyclohexen-1-yl)-3-buten-2-one Chemical compound CC(=O)C(\C)=C\C1C(C)=CCCC1(C)C JRJBVWJSTHECJK-PKNBQFBNSA-N 0.000 description 1
- UNDXPKDBFOOQFC-UHFFFAOYSA-N 4-[2-nitro-4-(trifluoromethyl)phenyl]morpholine Chemical compound [O-][N+](=O)C1=CC(C(F)(F)F)=CC=C1N1CCOCC1 UNDXPKDBFOOQFC-UHFFFAOYSA-N 0.000 description 1
- MBZRJSQZCBXRGK-UHFFFAOYSA-N 4-tert-Butylcyclohexyl acetate Chemical compound CC(=O)OC1CCC(C(C)(C)C)CC1 MBZRJSQZCBXRGK-UHFFFAOYSA-N 0.000 description 1
- QTBSBXVTEAMEQO-UHFFFAOYSA-M Acetate Chemical compound CC([O-])=O QTBSBXVTEAMEQO-UHFFFAOYSA-M 0.000 description 1
- 229910018072 Al 2 O 3 Inorganic materials 0.000 description 1
- 102000013142 Amylases Human genes 0.000 description 1
- 108010065511 Amylases Proteins 0.000 description 1
- 241000717739 Boswellia sacra Species 0.000 description 1
- 240000007436 Cananga odorata Species 0.000 description 1
- 239000005632 Capric acid (CAS 334-48-5) Substances 0.000 description 1
- 239000005635 Caprylic acid (CAS 124-07-2) Substances 0.000 description 1
- KXDHJXZQYSOELW-UHFFFAOYSA-N Carbamic acid Chemical class NC(O)=O KXDHJXZQYSOELW-UHFFFAOYSA-N 0.000 description 1
- 239000004215 Carbon black (E152) Substances 0.000 description 1
- BVKZGUZCCUSVTD-UHFFFAOYSA-L Carbonate Chemical compound [O-]C([O-])=O BVKZGUZCCUSVTD-UHFFFAOYSA-L 0.000 description 1
- 102000005575 Cellulases Human genes 0.000 description 1
- 108010084185 Cellulases Proteins 0.000 description 1
- NPBVQXIMTZKSBA-UHFFFAOYSA-N Chavibetol Natural products COC1=CC=C(CC=C)C=C1O NPBVQXIMTZKSBA-UHFFFAOYSA-N 0.000 description 1
- 244000223760 Cinnamomum zeylanicum Species 0.000 description 1
- WTEVQBCEXWBHNA-UHFFFAOYSA-N Citral Natural products CC(C)=CCCC(C)=CC=O WTEVQBCEXWBHNA-UHFFFAOYSA-N 0.000 description 1
- 241000207199 Citrus Species 0.000 description 1
- 235000008733 Citrus aurantifolia Nutrition 0.000 description 1
- 229920000858 Cyclodextrin Polymers 0.000 description 1
- 239000005770 Eugenol Substances 0.000 description 1
- 239000004863 Frankincense Substances 0.000 description 1
- 239000005792 Geraniol Substances 0.000 description 1
- GLZPCOQZEFWAFX-YFHOEESVSA-N Geraniol Natural products CC(C)=CCC\C(C)=C/CO GLZPCOQZEFWAFX-YFHOEESVSA-N 0.000 description 1
- SXRSQZLOMIGNAQ-UHFFFAOYSA-N Glutaraldehyde Chemical compound O=CCCCC=O SXRSQZLOMIGNAQ-UHFFFAOYSA-N 0.000 description 1
- 235000010254 Jasminum officinale Nutrition 0.000 description 1
- 240000005385 Jasminum sambac Species 0.000 description 1
- 239000004367 Lipase Substances 0.000 description 1
- 102000004882 Lipase Human genes 0.000 description 1
- 108090001060 Lipase Proteins 0.000 description 1
- 229920002774 Maltodextrin Polymers 0.000 description 1
- 244000062730 Melissa officinalis Species 0.000 description 1
- 235000010654 Melissa officinalis Nutrition 0.000 description 1
- 235000006679 Mentha X verticillata Nutrition 0.000 description 1
- 235000002899 Mentha suaveolens Nutrition 0.000 description 1
- 235000001636 Mentha x rotundifolia Nutrition 0.000 description 1
- 239000004435 Oxo alcohol Substances 0.000 description 1
- ABLZXFCXXLZCGV-UHFFFAOYSA-N Phosphorous acid Chemical class OP(O)=O ABLZXFCXXLZCGV-UHFFFAOYSA-N 0.000 description 1
- 235000008331 Pinus X rigitaeda Nutrition 0.000 description 1
- 241000018646 Pinus brutia Species 0.000 description 1
- 235000011613 Pinus brutia Nutrition 0.000 description 1
- 240000002505 Pogostemon cablin Species 0.000 description 1
- 235000011751 Pogostemon cablin Nutrition 0.000 description 1
- 229920002845 Poly(methacrylic acid) Polymers 0.000 description 1
- 229920000805 Polyaspartic acid Polymers 0.000 description 1
- 239000004793 Polystyrene Substances 0.000 description 1
- ZLMJMSJWJFRBEC-UHFFFAOYSA-N Potassium Chemical compound [K] ZLMJMSJWJFRBEC-UHFFFAOYSA-N 0.000 description 1
- UVMRYBDEERADNV-UHFFFAOYSA-N Pseudoeugenol Natural products COC1=CC(C(C)=C)=CC=C1O UVMRYBDEERADNV-UHFFFAOYSA-N 0.000 description 1
- 241000220317 Rosa Species 0.000 description 1
- MTCFGRXMJLQNBG-UHFFFAOYSA-N Serine Natural products OCC(N)C(O)=O MTCFGRXMJLQNBG-UHFFFAOYSA-N 0.000 description 1
- 102000012479 Serine Proteases Human genes 0.000 description 1
- 108010022999 Serine Proteases Proteins 0.000 description 1
- 229920002472 Starch Polymers 0.000 description 1
- QAOWNCQODCNURD-UHFFFAOYSA-L Sulfate Chemical compound [O-]S([O-])(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-L 0.000 description 1
- 235000011941 Tilia x europaea Nutrition 0.000 description 1
- GSEJCLTVZPLZKY-UHFFFAOYSA-N Triethanolamine Chemical compound OCCN(CCO)CCO GSEJCLTVZPLZKY-UHFFFAOYSA-N 0.000 description 1
- 238000005411 Van der Waals force Methods 0.000 description 1
- 238000002441 X-ray diffraction Methods 0.000 description 1
- LMETVDMCIJNNKH-UHFFFAOYSA-N [(3,7-Dimethyl-6-octenyl)oxy]acetaldehyde Chemical compound CC(C)=CCCC(C)CCOCC=O LMETVDMCIJNNKH-UHFFFAOYSA-N 0.000 description 1
- 229940022663 acetate Drugs 0.000 description 1
- 238000005903 acid hydrolysis reaction Methods 0.000 description 1
- 230000003213 activating effect Effects 0.000 description 1
- 239000013543 active substance Substances 0.000 description 1
- 239000000654 additive Substances 0.000 description 1
- 229910001420 alkaline earth metal ion Inorganic materials 0.000 description 1
- 238000005904 alkaline hydrolysis reaction Methods 0.000 description 1
- 239000012670 alkaline solution Substances 0.000 description 1
- 150000001336 alkenes Chemical class 0.000 description 1
- 150000008055 alkyl aryl sulfonates Chemical class 0.000 description 1
- 239000002168 alkylating agent Substances 0.000 description 1
- 229940100198 alkylating agent Drugs 0.000 description 1
- BJEPYKJPYRNKOW-UHFFFAOYSA-N alpha-hydroxysuccinic acid Natural products OC(=O)C(O)CC(O)=O BJEPYKJPYRNKOW-UHFFFAOYSA-N 0.000 description 1
- QUMXDOLUJCHOAY-UHFFFAOYSA-N alpha-methylbenzyl acetate Natural products CC(=O)OC(C)C1=CC=CC=C1 QUMXDOLUJCHOAY-UHFFFAOYSA-N 0.000 description 1
- WUOACPNHFRMFPN-UHFFFAOYSA-N alpha-terpineol Chemical compound CC1=CCC(C(C)(C)O)CC1 WUOACPNHFRMFPN-UHFFFAOYSA-N 0.000 description 1
- 150000003863 ammonium salts Chemical class 0.000 description 1
- 235000019418 amylase Nutrition 0.000 description 1
- 229940025131 amylases Drugs 0.000 description 1
- 229940011037 anethole Drugs 0.000 description 1
- PYKYMHQGRFAEBM-UHFFFAOYSA-N anthraquinone Natural products CCC(=O)c1c(O)c2C(=O)C3C(C=CC=C3O)C(=O)c2cc1CC(=O)OC PYKYMHQGRFAEBM-UHFFFAOYSA-N 0.000 description 1
- 239000001000 anthraquinone dye Substances 0.000 description 1
- 150000004056 anthraquinones Chemical class 0.000 description 1
- 230000000844 anti-bacterial effect Effects 0.000 description 1
- 230000000845 anti-microbial effect Effects 0.000 description 1
- 239000004599 antimicrobial Substances 0.000 description 1
- 239000000987 azo dye Substances 0.000 description 1
- 239000003899 bactericide agent Substances 0.000 description 1
- 239000000022 bacteriostatic agent Substances 0.000 description 1
- 239000011324 bead Substances 0.000 description 1
- 230000008901 benefit Effects 0.000 description 1
- 229940007550 benzyl acetate Drugs 0.000 description 1
- CADWTSSKOVRVJC-UHFFFAOYSA-N benzyl(dimethyl)azanium;chloride Chemical class [Cl-].C[NH+](C)CC1=CC=CC=C1 CADWTSSKOVRVJC-UHFFFAOYSA-N 0.000 description 1
- JGQFVRIQXUFPAH-UHFFFAOYSA-N beta-citronellol Natural products OCCC(C)CCCC(C)=C JGQFVRIQXUFPAH-UHFFFAOYSA-N 0.000 description 1
- 229920002988 biodegradable polymer Polymers 0.000 description 1
- 239000004621 biodegradable polymer Substances 0.000 description 1
- FZJUFJKVIYFBSY-UHFFFAOYSA-N bourgeonal Chemical compound CC(C)(C)C1=CC=C(CCC=O)C=C1 FZJUFJKVIYFBSY-UHFFFAOYSA-N 0.000 description 1
- 150000001720 carbohydrates Chemical class 0.000 description 1
- 235000014633 carbohydrates Nutrition 0.000 description 1
- BVKZGUZCCUSVTD-UHFFFAOYSA-N carbonic acid Chemical class OC(O)=O BVKZGUZCCUSVTD-UHFFFAOYSA-N 0.000 description 1
- 150000001735 carboxylic acids Chemical class 0.000 description 1
- 239000000969 carrier Substances 0.000 description 1
- 239000012876 carrier material Substances 0.000 description 1
- 230000015556 catabolic process Effects 0.000 description 1
- 239000003093 cationic surfactant Substances 0.000 description 1
- 229960000541 cetyl alcohol Drugs 0.000 description 1
- 239000010628 chamomile oil Substances 0.000 description 1
- 235000019480 chamomile oil Nutrition 0.000 description 1
- 239000003153 chemical reaction reagent Substances 0.000 description 1
- 235000017803 cinnamon Nutrition 0.000 description 1
- 239000001507 cistus ladaniferus l. oil Substances 0.000 description 1
- 229940043350 citral Drugs 0.000 description 1
- 229930003633 citronellal Natural products 0.000 description 1
- 235000000983 citronellal Nutrition 0.000 description 1
- 235000000484 citronellol Nutrition 0.000 description 1
- 235000020971 citrus fruits Nutrition 0.000 description 1
- 239000010634 clove oil Substances 0.000 description 1
- 239000013065 commercial product Substances 0.000 description 1
- 238000005056 compaction Methods 0.000 description 1
- 230000000052 comparative effect Effects 0.000 description 1
- 238000013329 compounding Methods 0.000 description 1
- 230000021615 conjugation Effects 0.000 description 1
- 239000000470 constituent Substances 0.000 description 1
- 229940019836 cyclamen aldehyde Drugs 0.000 description 1
- 229940097362 cyclodextrins Drugs 0.000 description 1
- 238000006731 degradation reaction Methods 0.000 description 1
- 230000003111 delayed effect Effects 0.000 description 1
- SQIFACVGCPWBQZ-UHFFFAOYSA-N delta-terpineol Natural products CC(C)(O)C1CCC(=C)CC1 SQIFACVGCPWBQZ-UHFFFAOYSA-N 0.000 description 1
- 238000000280 densification Methods 0.000 description 1
- 230000001419 dependent effect Effects 0.000 description 1
- 239000008121 dextrose Substances 0.000 description 1
- 229940095104 dimethyl benzyl carbinyl acetate Drugs 0.000 description 1
- 235000011180 diphosphates Nutrition 0.000 description 1
- 238000004851 dishwashing Methods 0.000 description 1
- 238000004090 dissolution Methods 0.000 description 1
- 125000003438 dodecyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])* 0.000 description 1
- 230000000694 effects Effects 0.000 description 1
- 238000002003 electron diffraction Methods 0.000 description 1
- DPUOLQHDNGRHBS-KTKRTIGZSA-N erucic acid Chemical class CCCCCCCC\C=C/CCCCCCCCCCCC(O)=O DPUOLQHDNGRHBS-KTKRTIGZSA-N 0.000 description 1
- 230000032050 esterification Effects 0.000 description 1
- 238000005886 esterification reaction Methods 0.000 description 1
- 150000002170 ethers Chemical class 0.000 description 1
- 238000007046 ethoxylation reaction Methods 0.000 description 1
- 229940071087 ethylenediamine disuccinate Drugs 0.000 description 1
- 229960002217 eugenol Drugs 0.000 description 1
- 239000004744 fabric Substances 0.000 description 1
- 235000019387 fatty acid methyl ester Nutrition 0.000 description 1
- 239000001148 ferula galbaniflua oil terpeneless Substances 0.000 description 1
- 239000001530 fumaric acid Substances 0.000 description 1
- 239000000417 fungicide Substances 0.000 description 1
- 230000001408 fungistatic effect Effects 0.000 description 1
- WTEVQBCEXWBHNA-JXMROGBWSA-N geranial Chemical compound CC(C)=CCC\C(C)=C\C=O WTEVQBCEXWBHNA-JXMROGBWSA-N 0.000 description 1
- 229940113087 geraniol Drugs 0.000 description 1
- 238000005858 glycosidation reaction Methods 0.000 description 1
- 229940015043 glyoxal Drugs 0.000 description 1
- 239000008187 granular material Substances 0.000 description 1
- HNDVDQJCIGZPNO-UHFFFAOYSA-N histidine Natural products OC(=O)C(N)CC1=CN=CN1 HNDVDQJCIGZPNO-UHFFFAOYSA-N 0.000 description 1
- 125000000487 histidyl group Chemical class [H]N([H])C(C(=O)O*)C([H])([H])C1=C([H])N([H])C([H])=N1 0.000 description 1
- 229910052739 hydrogen Chemical group 0.000 description 1
- 239000001257 hydrogen Chemical group 0.000 description 1
- 125000004435 hydrogen atom Chemical group [H]* 0.000 description 1
- 230000003301 hydrolyzing effect Effects 0.000 description 1
- 230000002209 hydrophobic effect Effects 0.000 description 1
- WPFVBOQKRVRMJB-UHFFFAOYSA-N hydroxycitronellal Chemical compound O=CCC(C)CCCC(C)(C)O WPFVBOQKRVRMJB-UHFFFAOYSA-N 0.000 description 1
- 239000004615 ingredient Substances 0.000 description 1
- 229930002839 ionone Natural products 0.000 description 1
- 150000002499 ionone derivatives Chemical class 0.000 description 1
- 239000001851 juniperus communis l. berry oil Substances 0.000 description 1
- 150000002596 lactones Chemical group 0.000 description 1
- 239000004571 lime Substances 0.000 description 1
- 235000001510 limonene Nutrition 0.000 description 1
- 229940087305 limonene Drugs 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
- 235000019421 lipase Nutrition 0.000 description 1
- 239000012263 liquid product Substances 0.000 description 1
- 230000005923 long-lasting effect Effects 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
- 238000005259 measurement Methods 0.000 description 1
- 230000010534 mechanism of action Effects 0.000 description 1
- 150000004702 methyl esters Chemical class 0.000 description 1
- 244000005700 microbiome Species 0.000 description 1
- 150000005673 monoalkenes Chemical class 0.000 description 1
- 239000001627 myristica fragrans houtt. fruit oil Substances 0.000 description 1
- 229940043348 myristyl alcohol Drugs 0.000 description 1
- 125000001421 myristyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 description 1
- GOQYKNQRPGWPLP-UHFFFAOYSA-N n-heptadecyl alcohol Natural products CCCCCCCCCCCCCCCCCO GOQYKNQRPGWPLP-UHFFFAOYSA-N 0.000 description 1
- BXWNKGSJHAJOGX-UHFFFAOYSA-N n-hexadecyl alcohol Natural products CCCCCCCCCCCCCCCCO BXWNKGSJHAJOGX-UHFFFAOYSA-N 0.000 description 1
- 238000006386 neutralization reaction Methods 0.000 description 1
- MGFYIUFZLHCRTH-UHFFFAOYSA-N nitrilotriacetic acid Chemical compound OC(=O)CN(CC(O)=O)CC(O)=O MGFYIUFZLHCRTH-UHFFFAOYSA-N 0.000 description 1
- 229960002446 octanoic acid Drugs 0.000 description 1
- JRZJOMJEPLMPRA-UHFFFAOYSA-N olefin Natural products CCCCCCCC=C JRZJOMJEPLMPRA-UHFFFAOYSA-N 0.000 description 1
- 229940055577 oleyl alcohol Drugs 0.000 description 1
- XMLQWXUVTXCDDL-UHFFFAOYSA-N oleyl alcohol Natural products CCCCCCC=CCCCCCCCCCCO XMLQWXUVTXCDDL-UHFFFAOYSA-N 0.000 description 1
- 150000007530 organic bases Chemical class 0.000 description 1
- 239000003973 paint Substances 0.000 description 1
- 125000000913 palmityl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 description 1
- RUVINXPYWBROJD-UHFFFAOYSA-N para-methoxyphenyl Natural products COC1=CC=C(C=CC)C=C1 RUVINXPYWBROJD-UHFFFAOYSA-N 0.000 description 1
- 229940067107 phenylethyl alcohol Drugs 0.000 description 1
- 229920000172 poly(styrenesulfonic acid) Polymers 0.000 description 1
- 229920005862 polyol Polymers 0.000 description 1
- 229920002223 polystyrene Polymers 0.000 description 1
- 229910052700 potassium Inorganic materials 0.000 description 1
- 239000011591 potassium Substances 0.000 description 1
- 159000000001 potassium salts Chemical class 0.000 description 1
- WSHYKIAQCMIPTB-UHFFFAOYSA-M potassium;2-oxo-3-(3-oxo-1-phenylbutyl)chromen-4-olate Chemical compound [K+].[O-]C=1C2=CC=CC=C2OC(=O)C=1C(CC(=O)C)C1=CC=CC=C1 WSHYKIAQCMIPTB-UHFFFAOYSA-M 0.000 description 1
- 239000002243 precursor Substances 0.000 description 1
- 239000002994 raw material Substances 0.000 description 1
- 239000012070 reactive reagent Substances 0.000 description 1
- 230000001603 reducing effect Effects 0.000 description 1
- 239000010670 sage oil Substances 0.000 description 1
- 239000010671 sandalwood oil Substances 0.000 description 1
- 229920006395 saturated elastomer Polymers 0.000 description 1
- 235000003441 saturated fatty acids Nutrition 0.000 description 1
- 150000003333 secondary alcohols Chemical class 0.000 description 1
- 125000003607 serino group Chemical group [H]N([H])[C@]([H])(C(=O)[*])C(O[H])([H])[H] 0.000 description 1
- 235000019832 sodium triphosphate Nutrition 0.000 description 1
- 239000000243 solution Substances 0.000 description 1
- 238000001228 spectrum Methods 0.000 description 1
- 235000019698 starch Nutrition 0.000 description 1
- 229940012831 stearyl alcohol Drugs 0.000 description 1
- 238000006277 sulfonation reaction Methods 0.000 description 1
- 150000003467 sulfuric acid derivatives Chemical class 0.000 description 1
- 150000003470 sulfuric acid monoesters Chemical class 0.000 description 1
- 238000004381 surface treatment Methods 0.000 description 1
- 235000020357 syrup Nutrition 0.000 description 1
- 239000006188 syrup Substances 0.000 description 1
- KUCOHFSKRZZVRO-UHFFFAOYSA-N terephthalaldehyde Chemical compound O=CC1=CC=C(C=O)C=C1 KUCOHFSKRZZVRO-UHFFFAOYSA-N 0.000 description 1
- 150000003505 terpenes Chemical class 0.000 description 1
- 235000007586 terpenes Nutrition 0.000 description 1
- 229940116411 terpineol Drugs 0.000 description 1
- 238000005809 transesterification reaction Methods 0.000 description 1
- 150000003626 triacylglycerols Chemical class 0.000 description 1
- 150000005691 triesters Chemical class 0.000 description 1
- 235000013311 vegetables Nutrition 0.000 description 1
- 239000010679 vetiver oil Substances 0.000 description 1
- ZFNVDHOSLNRHNN-UHFFFAOYSA-N xi-3-(4-Isopropylphenyl)-2-methylpropanal Chemical compound O=CC(C)CC1=CC=C(C(C)C)C=C1 ZFNVDHOSLNRHNN-UHFFFAOYSA-N 0.000 description 1
- 239000002888 zwitterionic surfactant Substances 0.000 description 1
Images
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
- C11D3/40—Dyes ; Pigments
Definitions
- the invention relates to a detergent composition, a detergent portion and use thereof for dyeing and washing textiles.
- Detergents for textiles are well known in the art. Frequent washing of coloreds is known to cause a gradual washout of the colors and the laundry loses color fastness.
- Reactive dyes are characterized by the fact that they bind to the fiber by covalent bonds. This gives them a high wash fastness. Effective reactive dyes must meet many requirements. For example, the dye molecules must be water-soluble and absorb in the desired wavelength range. In order to be able to bind to the fiber, the dye molecules have one or more identical or different anchor groups. These anchor groups must be capable of forming covalent bonds with the fiber, especially with free hydroxy groups of cellulose molecules. Effective reactive dyes are thus necessarily highly reactive towards nucleophiles and most suitable "alkylating agents".
- the high reactivity of the reactive anchor has the disadvantage that the reactive dye molecule can react not only with the textile fiber, ie the free hydroxy functionalities of the cellulose, but also with other nucleophiles. This can lead to a significant loss of reactive dye molecules.
- a reaction of water and in particular hydroxide anions takes place with the dye molecules. This requires the precise adjustment and control of the pH of the aqueous solution.
- Direct dyes are dyes characterized by non-covalent, e.g. van der Waals or ionic interaction interactions to which fiber is bound.
- the dye molecules In order to achieve a coloration of the fiber, the dye molecules must have a high affinity for the fiber to be dyed.
- the affinity of the direct dyes and thus the quality of the dyeing is usually significantly pH dependent. This requires accurate adjustment and control of the pH of the aqueous solution.
- Essential constituents of detergents are anionic and nonionic surfactants as well as builders or builders and carbonates.
- the detergent liquor, i. the aqueous detergent solution is usually basic.
- Modern detergents are added to suitable detergent enzymes which degrade contaminants mostly by hydrolytic cleavage.
- detergents especially amylases, lipases, cellulases and preferably proteases are used.
- the cleavage of contaminants is usually by reaction with particularly reactive nucleophilic groups in the active site of these enzymes.
- nucleophilic groups for example, in the case of the well-studied serine proteases in the active center, besides the nucleophilic hydroxyl group of the reactive serine, there is a basic histidine side group. This histidine residue has an activating effect on the nucleophiles of the hydroxyl group of the serine residue.
- the high reactivity of the nucleophilic hydroxyl group causes not only the efficient cleavage of dirt molecules, but also side reactions with possibly existing other molecules. Due to their usually high nucleophiles, the enzymes used are particularly susceptible to undesirable side reactions with reactive groups, such as those present as anchor groups in reactive dyes. It is also known that reactive reagents covalently bind to the nucleophilic group of the enzyme and irreversibly inhibit the enzyme and thus render it useless.
- reactive dyes as colorants with detergents suggests that it may be enhanced by nucleophiles in the detergent liquor, e.g. Hydroxy or surfactant anions, cleavage and thus to make unusable the reactive dye before it can bind to the fiber.
- nucleophiles in the detergent liquor e.g. Hydroxy or surfactant anions
- Detergent compositions which may contain limited dyes are known in the art. However, these dyes are merely used to give the detergent a more visually pleasing color, much as fragrances can be used to impart a more pleasant odor to the detergent composition. However, the detergent compositions known from the prior art are not suitable for enabling freshening of already washed-out colors without significantly impairing the washing result.
- the object of the present invention is therefore to provide a detergent composition and a process which are suitable not only to largely avoid a loss of color fastness, but in particular to enable a refreshing of already washed out colors without substantially impairing the washing result Wash off the refreshed paint in the following washes.
- the object of the invention is achieved by a comprising at least one first reactive dye and at least one first direct dye.
- the term "about” in the case of numerical values or ranges of values is understood to indicate a tolerance range which the person skilled in the art will consider customary.
- the term “about” is to be understood as meaning a tolerance range for value or value ranges of ⁇ 20%, preferably ⁇ 10%, and more preferably ⁇ 5%, specified in the invention.
- % by weight is used for percentages by weight and, unless stated otherwise, in each case based on the total amount of the composition.
- Reactive dyes are preferably present in an amount of about 0.1 to about 15 weight percent, preferably to about 10 weight percent, more preferably in an amount of about 0.28 to about 8.2 weight percent, more preferably in an amount of about 0.46 to about 6.4 weight percent, more preferably in an amount of about 0.64 to about 4.6 weight percent, and even more preferably in an amount of about 0.82 to about 2.8 wt .-% before.
- Direct dyes are preferably present in an amount of about 0.1 to about 15 weight percent, preferably to about 10 weight percent, more preferably in an amount of about 0.24 to about 8.16 weight percent, more preferably in an amount of about 0.38 to about 6.32 weight percent, more preferably in an amount of about 0.52 to about 4.48 weight percent, and even more preferably in an amount of about 0.66 to about 2.64 wt .-% before.
- Fixers are preferably present in an amount of about 0.1 to about 30 weight percent, more preferably in an amount of about 1.8 to about 25 weight percent, more preferably in an amount of about 2.6 to about 20 Wt .-%, more preferably in an amount of about 3.4 to about 15% by weight, and more preferably in an amount of about 4.2 to about 10% by weight.
- Builders are preferably present in an amount of about 0.1 to about 10 weight percent, more preferably in an amount of about 0.5 to about 8.4 weight percent, more preferably in an amount of about 1.0 to about 6.8 wt .-%, more preferably in an amount of about 1.6 to about 5.2 wt .-%, and even more preferably in an amount of about 1.8 to about 3.6 wt .-% before ,
- Surfactants are preferably present in an amount of about 0.3 to about 20 weight percent, more preferably in an amount of about 0.64 to about 16.4 weight percent, more preferably in an amount of about 0.98 to about about 12.8 weight percent, more preferably about 1.32 to about 9.2 weight percent, and even more preferably about 1.66 to about 5.6 weight percent in front.
- Soaps are preferably present in an amount of about 0.1 to about 5 weight percent, more preferably in an amount of about 0.18 to about 4.1 weight percent, more preferably in an amount of about 0.26 to about about 3.2 wt.%, more preferably in an amount of about 0.34 to about 2.3 wt.%, and even more preferably in an amount of about 0.42 to about 1.4 wt.% in front.
- Enzymes are preferably present in an amount of from about 0 to about 1 weight percent, more preferably in an amount of from about 0.01 to about 1 weight percent, more preferably in an amount of from about 0.02 to about 0.82 Wt .-%, more preferably in an amount of about 0.04 to about 0.64 wt .-%, more preferably in an amount of about 0.06 to about 0.46 wt .-%, and still more preferably in in an amount of about 0.08 to about 0.28 wt%.
- Chelating agents are preferably present in an amount of from 0.2 to 5 weight percent, more preferably in an amount of from about 0.36 to about 4.2 weight percent, more preferably in an amount of from about 0.52 to about 3 , 4 wt .-%, more preferably in an amount of about 0.68 to about 2.6 Wt .-%, and more preferably in an amount of about 0.84 to about 1.8 wt .-% before.
- Sodium carbonate is preferably present in an amount of from about 0 to about 20 weight percent, more preferably in an amount of from about 0.68 to about 16.68 weight percent, more preferably in an amount of from about 1.36 to about about 13.36 wt.%, more preferably in an amount of about 2.04 to about 10.04 wt.%, and even more preferably in an amount of about 2.72 to about 6.72 wt.% in front.
- compositions disclosed in the present application i. those compositions, the components of which are not definitively defined in terms of quantity, expediently to be completed with further substances known to the person skilled in the art either from other parts of the description or from the prior art.
- the open compositions disclosed in the present application are completed with a sodium salt, preferably sodium chloride and / or sodium sulfate, and most preferably a mixture of sodium chloride and sodium sulfate, to 100 wt%, wherein the proportion of sodium chloride is preferably at least 50% by weight, more preferably at least 70% by weight, more preferably at least 80% by weight and even more preferably at least 90% by weight of the total amount of sodium sulfate and sodium used -Chlorid makes up.
- a sodium salt preferably sodium chloride and / or sodium sulfate, and most preferably a mixture of sodium chloride and sodium sulfate, to 100 wt%, wherein the proportion of sodium chloride is preferably at least 50% by weight, more preferably at least 70% by weight, more preferably at least 80% by weight and even more preferably at least 90% by weight of the total amount of sodium sulfate and sodium used -Chlorid makes up.
- the reactive dyes are preferably as vinylsulfone dyes and more preferably as reactive red, reactive yellow, reactive blue, reactive green or even more preferably reactive black, preferably reactive black 5, or combinations of these.
- the direct dyes are preferably present as acid dyes and more preferably as direct blue, direct red, direct yellow or direct black, preferably direct black 22, or as combinations of these.
- the fixers are preferably present as silicates and more preferably as sodium metasilicate.
- the builders are preferably present as zeolites.
- the surfactants are preferred as anionic and nonionic surfactants.
- the chelating agent is preferably trilon.
- the enzymes are preferably present as proteases.
- the soaps are preferably present as fatty acid soaps.
- the detergent compositions according to the invention may contain surface-active substances from the group of anionic, nonionic, zwitterionic or cationic surfactants.
- Anionic surfactants and nonionic surfactants are preferred.
- anionic surfactants for example, those of the sulfonate type and sulfates are used.
- surfactants of the sulfonate type preferably come C9-1 3- alkylbenzenesulfonates, olefin sulfonates, d.
- H Mixtures of alkene and hydroxyalkanesulfonates and disulfonates into consideration, as obtained for example from C12-18 monoolefins having terminal or internal double bond by sulfonating with gaseous sulfur trioxide and subsequent alkaline or acidic hydrolysis of the sulfonation.
- alkanesulfonates which are obtained from C12-18-alkanes, for example by sulfochlorination or sulfoxidation with subsequent hydrolysis or neutralization.
- esters of 2-sulfo fatty acids esters of 2-sulfo fatty acids (ester sulfonates), z.
- the 2-sulfonated methyl esters of hydrogenated coconut, palm kernel or tallow fatty acids suitable.
- sulfated fatty acid glycerol esters are to be understood as meaning mono-, di- and triesters and mixtures thereof, as obtained in the preparation by esterification of a monoglycerol with 1 to 3 moles of fatty acid or in the transesterification of triglycerides with 0.3 to 2 moles of glycerol.
- Preferred sulfated fatty acid glycerol esters are the sulfate products of saturated fatty acids having 6 to 22 carbon atoms, for example caproic acid, caprylic acid, capric acid, myristic acid, lauric acid, palmitic acid, stearic acid or behenic acid.
- alk (en) ylsulfates are the alkali metal salts and in particular the sodium salts of the sulfuric monoesters of the C 12 -C 18 -fatty alcohols, for example of coconut fatty alcohol, tallow fatty alcohol, lauryl, myristyl, cetyl or Stearyl alcohol or C10-C20 oxo alcohols and those half-esters of secondary alcohols of these chain lengths are preferred.
- alk (en) ylsulfates of said chain length which contain a synthetic, produced on a petrochemical basis straight-chain alkyl radical, which have an analogous degradation behavior as the adequate compounds based on oleochemical raw materials.
- alk (en) ylsulfates of said chain length which contain a synthetic, produced on a petrochemical basis straight-chain alkyl radical, which have an analogous degradation behavior as the adequate compounds based on oleochemical raw materials.
- C12-C16 alkyl sulfates and C12-C15 alkyl sulfates and C14-C15 alkyl sulfates are preferred.
- sulfuric acid monoesters of straight-chain or branched C7-21 alcohols ethoxylated with from 1 to 6 moles of ethylene oxide such as 2-methyl-branched C9-11 alcohols having on average 3.5 moles of ethylene oxide (EO) or C12-18 fatty alcohols with 1 up to 4 mol EO, are suitable.
- Suitable anionic surfactants are also the salts of alkylsulfosuccinic acid, which are also referred to as sulfosuccinates or as sulfosuccinic esters, and monoesters and / or diesters of sulfosuccinic acid with alcohols, preferably fatty alcohols and in particular ethoxylated fatty alcohols.
- alcohols preferably fatty alcohols and in particular ethoxylated fatty alcohols.
- Preferred sulfosuccinates contain C8-18 fatty alcohol residues or mixtures of these.
- Particularly preferred sulfosuccinates contain a fatty alcohol residue derived from ethoxylated fatty alcohols, which in themselves constitute nonionic surfactants (see description below).
- Sulfosuccinates whose fatty alcohol residues are derived from ethoxylated fatty alcohols with a narrow homolog distribution, are again particularly preferred.
- alk (en) ylsuccinic acid having preferably 8 to 18 carbon atoms in the alk (en) yl chain or salts thereof.
- anionic surfactants are particularly soaps into consideration.
- Suitable are saturated fatty acid soaps, such as the salts of lauric acid, myristic acid, palmitic acid, stearic acid, hydrogenated erucic acid and behenic acid and in particular from natural fatty acids, for. Coconut, palm kernel or tallow fatty acids, derived soap mixtures.
- the anionic surfactants including the soaps may be in the form of their sodium, potassium or ammonium salts and as soluble salts of organic bases such as mono-, di- or Triethanolamine.
- the anionic surfactants are preferably present in the form of their sodium or potassium salts, in particular in the form of the sodium salts.
- surfactants are used in the form of their magnesium salts.
- the nonionic surfactants used are preferably alkoxylated, advantageously ethoxylated, in particular primary, alcohols having preferably 8 to 18 carbon atoms and on average 1 to 12 moles of ethylene oxide (EO) per mole of alcohol, in which the alcohol radical can be linear or preferably methyl-branched in the 2-position or linear and methyl-branched radicals in the mixture can contain, as they are usually present in Oxoalkoholresten.
- EO ethylene oxide
- Examples of preferred ethoxylated alcohols include C12-14 alcohols with 3 moles EO or 4 moles EO, C9-11 alcohols with 7 moles EO, C13-15 alcohols with 3 moles EO, 5 moles EO, 7 moles EO or 8 Moles of EO, C12-18 alcohols with 3 moles of EO, 5 moles of EO or 7 moles of EO and mixtures thereof, and mixtures of C12-14-alcohol with 3 moles of EO and C12-18-alcohol with 5 moles of EO.
- the degrees of ethoxylation given represent statistical means which, for a particular product, may be an integer or a fractional number.
- Preferred alcohol ethoxylates have a narrow homolog distribution (narrow range ethoxylates, NRE).
- fatty alcohols containing more than 12 moles of EO can also be used. Examples include tallow fatty alcohol with 14 moles of EO, 25 moles of EO, 30 moles of EO or 40 moles of EO.
- nonionic surfactants used either as the sole nonionic surfactant or in combination with other nonionic surfactants are alkoxylated, preferably ethoxylated or ethoxylated and propoxylated fatty acid alkyl esters, preferably having from 1 to 4 carbon atoms in the alkyl chain, especially fatty acid methyl esters.
- alkyl polyglycosides APG
- Applicable alkylpolyglycosides satisfy the general formula RO (G) Z in which R is a linear or branched, in particular in the 2-position methyl branched, saturated or unsaturated, aliphatic radical having 8 to 22, preferably 12 to 18 carbon atoms and G is the symbol which represents a glycose unit having 5 or 6 C atoms, preferably glucose.
- the degree of glycosidation z is between 1.0 and 4.0, preferably between 1.0 and 2.0 and in particular between 1.1 and 1.4.
- Suitable crystalline, layered sodium silicates have the general formula NaMSi x O 2x + 1 . H 2 O, where M is sodium or hydrogen, x is a number from 1.9 to 4 and y is a number from 0 to 20 and preferred values for x are 2, 3 or 4.
- Preferred crystalline layered silicates of the formula given are those in which M is sodium and x assumes the values 2 or 3.
- both beta; and delta-sodium disilicates are Na 2 Si 2 O 5 . y H 2 O preferred.
- amorphous sodium silicates with a Na 2 O: SiO 2 modulus of from 1: 2 to 1: 3.3, preferably from 1: 2 to 1: 2.8 and in particular from 1: 2 to 1: 2.6, which Delayed and have secondary washing properties.
- the dissolution delay over conventional amorphous sodium silicates may have been caused in various ways, for example by surface treatment, compounding, compaction / densification or by overdrying.
- the term "amorphous” is also understood to mean "X-ray amorphous”.
- the silicates do not give sharp X-ray reflections typical of crystalline substances but at best one or more maxima of the scattered X-rays having a width of several degrees of diffraction angle. It can lead to particularly good builder properties if the silicate particles provide blurred or even sharp diffraction maxima in electron diffraction experiments. This is to be interpreted as meaning that the products have microcrystalline regions of size about 10 to about several hundred nm, with values up to max. about 50 nm and especially up to max. about 20 nm are preferred. Particularly preferred are compacted / compacted amorphous silicates, compounded amorphous silicates and overdried X-ray amorphous silicates.
- a fine crystalline, synthetic and bound water-containing zeolite optionally used is preferably zeolite A and / or P.
- Zeolite MAP eg, commercial product: Doucil A24 from Crosfield
- zeolite X and mixtures of the zeolites A, X and / or P are particularly preferred.
- Commercially available and preferably usable in the context of the present invention is, for example, also a cocrystal of zeolite X and zeolite A (about 80% by weight).
- Zeolite X) represented by the formula nNa 2 O. (1-n) K 2 O. Al 2 O 3 . (2-2.5) SiO 2.
- Suitable zeolites have an average particle size of less than about 10 microns (volume distribution, Coulter Counter method) and preferably contain from about 18 to about 22 weight percent, more preferably from about 20 to about 22 weight percent bound water.
- phosphates In detergents, it is also possible to use generally known phosphates as builders, if such an application should not be avoided for ecological reasons. Particularly suitable are the sodium salts of orthophosphates, pyrophosphates and in particular tripolyphosphates.
- Useful organic builder substances are, for example, the polycarboxylic acids which can be used in the form of their sodium salts, polycarboxylic acids meaning those carboxylic acids which carry more than one acid function. These are, for example, citric acid, adipic acid, succinic acid, glutaric acid, malic acid, tartaric acid, maleic acid, fumaric acid, sugar acids, aminocarboxylic acids, nitrilotriacetic acid (NTA), provided their use is not objectionable for ecological reasons, and mixtures of these.
- Preferred salts are the salts of polycarboxylic acids such as citric acid, adipic acid, succinic acid, glutaric acid, tartaric acid, sugar acids and mixtures thereof.
- the acids themselves can also be used.
- the acids typically also have the property of an acidifying component and thus also serve for Adjustment of a lower and milder pH of washing and cleaning agent portions according to the invention.
- citric acid, succinic acid, glutaric acid, adipic acid, gluconic acid and any mixtures of these are to be mentioned in this context.
- polymeric polycarboxylates are suitable. These are, for example, the alkali metal salts of polyacrylic acid or polymethacrylic acid, for example, those having a molecular weight of about 500 to about 70,000 g / mol.
- the molecular weights stated for polymeric polycarboxylates are weight average molecular weights MW of the particular acid form, which were determined in principle by means of gel permeation chromatography (GPC), a UV detector being used. The measurement was carried out against an external polyacrylic acid standard, which provides realistic molecular weight values due to its structural relationship with the polymers investigated. These data differ significantly from the molecular weight data, in which polystyrene sulfonic acids are used as standard.
- Suitable polymers are in particular polyacrylates which preferably have a molecular weight of about 2,000 to about 20,000 g / mol. Because of their superior solubility, the short-chain polyacrylates which have molecular weights of from about 2,000 to about 10,000 g / mol, more preferably from about 3,000 to about 5,000 g / mol, may in turn be preferred from this group.
- copolymeric polycarboxylates in particular those of acrylic acid with methacrylic acid or of acrylic acid or methacrylic acid with maleic acid.
- Copolymers of acrylic acid with maleic acid which contain 50 to 90% by weight of acrylic acid and 50 to 10% by weight of maleic acid have proven to be particularly suitable.
- Their relative molecular weight, based on free acids, is generally from 2,000 to 70,000 g / mol, preferably from 20,000 to 50,000 g / mol and in particular from about 30,000 to about 40,000 g / mol.
- the (co) polymers Polycarboxylates can be used either as a powder or as an aqueous solution.
- the polymers may also contain allylsulfonic acids such as allyloxybenzenesulfonic acid and methallylsulfonic acid as a monomer.
- allylsulfonic acids such as allyloxybenzenesulfonic acid and methallylsulfonic acid
- biodegradable polymers from more than two different monomer units are also preferred.
- polymeric aminodicarboxylic acids their salts or their precursors.
- polyaspartic acids or their salts and derivatives are particularly preferred.
- polyacetals which can be obtained by reacting dialdehydes with polyolcarboxylic acids having 5 to 7 carbon atoms and at least 3 hydroxyl groups.
- Preferred polyacetals are obtained from dialdehydes such as glyoxal, glutaraldehyde, terephthalaldehyde and mixtures thereof and from polyol carboxylic acids such as gluconic acid and / or glucoheptonic acid.
- dextrins for example oligomers or polymers of carbohydrates, which can be obtained by partial hydrolysis of starches.
- the hydrolysis can be carried out by customary, for example acid or enzyme catalyzed processes.
- they are hydrolysis products having average molecular weights in the range of about 400 to about 500,000 g / mol.
- DE dextrose equivalent
- Both maltodextrins with a DE of between 3 and 20 and dry glucose syrups with a DE of between about 20 and about 37 and also so-called yellow dextrins and white dextrins with relatively high molecular weights in the range from about 2,000 to about 30,000 g / mol are useful.
- organic co-builders are, for example, acetylated hydroxycarboxylic acids or salts thereof, which may optionally also be present in lactone form and which contain at least 4 carbon atoms and at least one hydroxyl group and a maximum of two acid groups.
- Another class of substances with co-builder properties are phosphonates.
- Perfumes are used in the detergent composition of the present invention to improve the overall olfactory impression of the products.
- fragrance compounds can be used, for example the synthetic products of the ester, ether, aldehyde, ketone, alcohol and hydrocarbon type.
- Fragrance compounds of the ester type are, for example, benzyl acetate, phenoxyethyl isobutyrate, p-t-butylcyclohexyl acetate, linalyl acetate, dimethylbenzylcarbinylacetate, phenylethylacetate, linalylbenzoate, benzylformate, ethylmethylphenylglycinate, allylcyclohexylpropionate, styrallylpropionate and benzylsalicylate.
- Ethers include, for example, benzyl ethyl ether.
- the aldehydes include, for. B. linear alkanals having 8 to 18 carbon atoms, citral, citronellal, citronellyloxyacetaldehyde, cyclamen aldehyde, hydroxycitronellal, purple and bourgeonal.
- the ketones include the ionones, alpha-isomethylionone, and methyl cedryl ketone.
- To the alcohols include anethole, citronellol, eugenol, geraniol, linalool, phenylethyl alcohol and terpineol.
- the hydrocarbons mainly include terpenes such as limonene and pinene. Preference is given to using mixtures of different fragrances which are adapted to one another in such a way that together they produce an attractive fragrance note.
- perfume oils may also contain natural fragrance mixtures as are available from vegetable sources. Examples are pine, citrus, jasmine, patchouli, rose or ylang-ylang oil. Also suitable are nutmeg oil, sage oil, chamomile oil, clove oil, lemon balm oil, mint oil, cinnamon leaf oil, lime blossom oil, juniper berry oil, vetiver oil, olibanum oil, galbanum oil and labdanum oil and orange blossom oil, neroliol, orange peel oil and sandalwood oil.
- the fragrances can be incorporated directly into the detergent preparations; but it may also be advantageous to apply the fragrances on carriers that enhance the adhesion of the perfume on the laundry and provide by a slower release of fragrance for long-lasting fragrance of the textiles.
- carrier materials for example, cyclodextrins have been proven.
- the cyclodextrin-perfume complexes can additionally be coated with other auxiliaries.
- the detergent composition according to the invention may contain antimicrobial agents.
- antimicrobial agents Depending on the antimicrobial spectrum and mechanism of action, a distinction is made between bacteriostatic agents and bactericides, fungistatics and fungicides, etc.
- Important substances from these groups are, for example, benzalkonium chlorides, alkylarylsulfonates, halophenols and phenolmercuric acetate.
- the reactive dyes preferably have an alkylating group. More preferably, the reactive dyes have a triazine and / or vinylsulfone group as an anchor group, with a vinylsulfone group being particularly preferred.
- Preferred direct dyes are dyes from the group of azo dyes and anthraquinone dyes.
- Preferred direct dyes are anionic (acid dyes). Further preferred are anionic azo and Anthrachinonsulfonate.
- Anionic dyes ("acid dyes") in the context of the present invention are organic salts whose anion absorbs light.
- Preferred direct dyes are substantive dyes. Their liability is almost exclusively due to van der Waals forces. More preferred are azo and anthraquinone direct dyes.
- the direct dye molecules preferably have a conjugation system with at least 8 double bonds. These are preferably hydrophobic on one side and flat. Particularly preferred as a direct dye is Direct Black 22.
- black dyes but reactive and / or direct dyes of a different color may also be used, for example to obtain a dark blue color refreshment. But also yellow, green, red, blue and / or other dyes, such as Reactive Red, Reactive Yellow, Reactive Blue, Reactive Green and their combinations are conceivable. The desired colors can also be achieved by a combination of different dyes.
- Another aspect of the invention relates to detergent portions wherein the detergent composition of the invention is formulated in metered portions.
- the detergent composition is particulate, more preferably in the form of powder, granules or beads.
- the detergent portions are preferably in the form of shaped bodies, and these are more preferably shaped as tablets ("tabs"), cuboids, briquettes, etc., which are dosed as a whole into the liquor.
- the detergent portions are present as liquid products, and these more preferably with a water-soluble sheaths, which dissolve upon contact with the aqueous liquor and release the contents into the liquor.
- any ingredient of the mixture e.g. the reactive dye, consist of a compound or a mixture of compounds.
- the reactive dye consist of a compound or a mixture of compounds.
- a preferred detergent composition comprises reactive dye, preferably as vinyl sulfone dye, in an amount of about 0.1 to about 10 weight percent, direct dye, preferably as an acid dye, in an amount of about 0.1 to about 10 weight percent, and fixer , preferably as sodium metasilicate, in an amount of about 1 to about 30% by weight.
- a preferred detergent composition comprises reactive dye, preferably as vinyl sulfone dye, in an amount of about 0.1 to about 10% by weight, direct dye, preferably as acid dye, in an amount of about 0.1 to about 10% by weight, and fixer , preferably as sodium metasilicate, in an amount of about 1 to about 30% by weight, and builder, preferably as zeolites, in an amount of about 0.1 to about 10% by weight.
- a preferred detergent composition comprises reactive dye, preferably as vinyl sulfone dye, in an amount of about 0.1 to about 10% by weight, direct dye, preferably as acid dye, in an amount of about 0.1 to about 10% by weight, and fixer , preferably as sodium metasilicate, in an amount of about 1 to about 30% by weight, builder, preferably as zeolites, in an amount of about 0.1 to about 10% by weight and surfactants, preferably as anionic and nonionic Surfactants, in an amount of about 0.3 to about 20 wt .-%.
- a preferred detergent composition comprises reactive dye, preferably as vinyl sulfone dye, in an amount of about 0.1 to about 10% by weight, direct dye, preferred as an acid dye, in an amount of about 0.1 to about 10 wt .-%, and fixers, preferably as sodium metasilicate, in an amount of about 1 to about 30 wt .-%, builder, preferably as zeolites, in an amount of from about 0.1% to about 10%, by weight, surfactants, preferably as anionic and nonionic surfactants, in an amount from about 0.3% to about 20% by weight, and soaps, preferably as fatty acid soaps, in an amount of about 0.1 to about 5 wt .-%.
- a preferred detergent composition comprises reactive dye, preferably as vinyl sulfone dye, in an amount of about 0.1 to about 10% by weight, direct dye, preferably as acid dye, in an amount of about 0.1 to about 10% by weight, and fixer , preferably as sodium metasilicate, in an amount of about 1 to about 30% by weight, builder, preferably as zeolites, in an amount of about 0.1 to about 10% by weight, surfactants, preferably as anionic and nonionic Surfactants, in an amount of about 0.3 to about 20% by weight, of soaps, preferably as fatty acid soaps, in an amount of about 0.1 to about 5% by weight, and enzymes, preferably as proteases, in an amount from about 0.01 to about 1% by weight.
- reactive dye preferably as vinyl sulfone dye
- direct dye preferably as acid dye
- fixer preferably as sodium metasilicate
- builder preferably as zeolites
- surfactants preferably as anionic and nonionic Surfactants
- soaps
- a preferred detergent composition comprises reactive dye, preferably as vinyl sulfone dye, in an amount of about 0.1 to about 10% by weight, direct dye, preferably as acid dye, in an amount of about 0.1 to about 10% by weight, and fixer , preferably as sodium metasilicate, in an amount of about 1 to about 30% by weight, builder, preferably as zeolites, in an amount of about 0.1 to about 10% by weight, surfactants, preferably as anionic and nonionic Surfactants, in an amount of about 0.3 to about 20% by weight, of soaps, preferably as fatty acid soaps, in an amount of about 0.1 to about 5% by weight, of enzymes, preferably as proteases, in an amount from about 0.01 to about 1 weight percent and chelating agents, preferably as trilon, in an amount of about 0.2 to about 5 weight percent.
- reactive dye preferably as vinyl sulfone dye
- direct dye preferably as acid dye
- fixer preferably as sodium metasilicate
- builder preferably as ze
- a preferred detergent composition comprises reactive dye, preferably as vinyl sulfone dye, in an amount of about 0.1 to about 10% by weight, direct dye, preferably as acid dye, in an amount of about 0.1 to about 10% by weight, and fixer . preferably as sodium metasilicate, in an amount of about 1 to about 30% by weight, builder, preferably as zeolites, in an amount of about 0.1 to about 10% by weight, surfactants, preferably as anionic and nonionic surfactants , in an amount of from about 0.3 to about 20% by weight, of soaps, preferably as fatty acid soaps, in an amount of from about 0.1 to about 5% by weight, of enzymes, preferably as proteases, in an amount of from about 0.01% to about 1% by weight of chelating agent, preferably as trilon, in an amount of about 0.2 to about 5% by weight and carbonate, preferably as sodium carbonate, in an amount of about 0.01 to about 20% by weight.
- reactive dye preferably as vinyl sulfone dye
- Another preferred detergent composition comprises reactive dye, preferably as vinylsulfone dye, in an amount of about 0.5 to 3% by weight, direct dye, preferably as acid dye, in an amount of about 0.5 to about 3% by weight, and fixer , preferably as sodium metasilicate, in an amount of about 1 to about 15% by weight, builder, preferably as zeolites, in an amount of about 0.1 to about 2% by weight, surfactants, preferably as anionic and nonionic Surfactants, in an amount of about 0.5 to about 15 wt .-% and sodium chloride and / or sodium sulfate, in an amount of about 60 to 90 wt .-%.
- reactive dye preferably as vinylsulfone dye
- direct dye preferably as acid dye
- fixer preferably as sodium metasilicate
- builder preferably as zeolites
- surfactants preferably as anionic and nonionic Surfactants
- Reactive Black 5 was used as a reactive dye in an amount of about 10% by weight, and Direct Black 22 as a direct dye in an amount of about 10% by weight. It was sodium metasilicate in an amount of about 30 wt .-%, zeolites in an amount of about 10 wt .-%, anionic and nonionic surfactants in an amount of about 20 wt .-%, soaps in an amount of about 5 Wt .-%, enzymes in an amount of about 1 wt .-%, trilone in an amount of 5 wt .-%, and sodium carbonate used in an amount of about 20 wt .-%. With sodium chloride was adjusted to 100Gew .-%.
- Reactive Black 5 as a reactive dye in an amount of about 0.1% by weight
- Direct Black 22 as a direct dye in an amount of about 0.1% by weight
- Zeolites in an amount of about 1% by weight
- anionic and nonionic surfactants in an amount of about 0.3% by weight
- soaps in an amount of about 0.1% by weight
- trilon was in an amount used by about 0.2 wt .-%.
- sodium chloride was adjusted to 100 wt .-%.
- Reactive Black 5 as a reactive dye in an amount of about 1% by weight
- Direct Black 22 as a direct dye in an amount of about 0.8% by weight. It was sodium metasilicate in an amount of about 5 wt .-%, zeolites in an amount of about 2 wt .-%, anionic and nonionic surfactants in an amount of about 2 wt .-%, soaps in an amount of about 0 , 5 wt%, enzymes in an amount of about 0.1 wt%, trilon in an amount of about 1 wt%, and sodium carbonate in an amount of about 3.4 wt% , Sodium chloride was used in an amount of about 82.2% by weight and sodium sulfate in an amount of about 2% by weight.
- Fig. 1 A and B show photographic results of the comparative experiments described.
- compositions were examined. All compositions contained 450 g of sodium chloride (about 80% by weight), 50 g of metasilicate (about 9% by weight) and 56 g of " Ariel® Color” (about 10% by weight). " Ariel® Color” is a detergent composition known to those skilled in the art.
- Composition 1 also contained 5 grams (about 1 weight percent) Remazol Deep Black N 150 (Reactive Black 5).
- Composition 2 contained 4 g (about 1% by weight) Sirius Black VSF / hc (Direct Black 22).
- Composition 3 contained both 5 grams Remazol Deep Black N 150 (about 1 weight percent) and 4 grams Sirius Black VSF / hc (about 1 weight percent).
- Fig. 1 A shows the result of washing a "plain" cotton sheet.
- Fig. 1 B shows the result of the laundry of mercerized cotton (tablecloth fabric). It can be seen that composition 3 gives the best dyeing result in both test series. Thus, color fastness and hiding power of composition 3 is improved, not only in comparison with the result according to compositions 1 and 2 taken alone, but also in comparison with their (imaginary) superposition.
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)
- Detergent Compositions (AREA)
- Coloring (AREA)
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
PL15194014T PL3020794T3 (pl) | 2014-11-12 | 2015-11-11 | Kompozycja środka piorącego i jej zastosowanie |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
DE102014016675.9A DE102014016675B4 (de) | 2014-11-12 | 2014-11-12 | Waschmittelzusammensetzung, Verwendung derselben und Waschmittelportion |
Publications (3)
Publication Number | Publication Date |
---|---|
EP3020794A2 true EP3020794A2 (fr) | 2016-05-18 |
EP3020794A3 EP3020794A3 (fr) | 2016-06-08 |
EP3020794B1 EP3020794B1 (fr) | 2020-02-19 |
Family
ID=54540918
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
EP15194014.5A Active EP3020794B1 (fr) | 2014-11-12 | 2015-11-11 | Composition de lessive et son utilisation |
Country Status (3)
Country | Link |
---|---|
EP (1) | EP3020794B1 (fr) |
DE (1) | DE102014016675B4 (fr) |
PL (1) | PL3020794T3 (fr) |
Families Citing this family (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
DE102015119949B4 (de) * | 2015-11-18 | 2024-08-14 | Brauns-Heitmann Gmbh & Co. Kg | Verwendung eines farbabgebendes Produktes zum Färben von oder Auffrischen von Färbungen in textilen Materialien |
Family Cites Families (7)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US4994193A (en) * | 1988-12-15 | 1991-02-19 | The Procter & Gamble Company | Liquid fabric softener |
EP1201743A1 (fr) * | 2000-10-31 | 2002-05-02 | The Procter & Gamble Company | Compositions détergentes |
GB0421145D0 (en) * | 2004-09-23 | 2004-10-27 | Unilever Plc | Laundry treatment compositions |
ATE523584T1 (de) * | 2007-01-26 | 2011-09-15 | Unilever Nv | Nuancierungsmittel |
US8673836B2 (en) * | 2007-03-20 | 2014-03-18 | The Procter & Gamble Company | Laundry detergent composition with a reactive dye |
US8021436B2 (en) | 2007-09-27 | 2011-09-20 | The Procter & Gamble Company | Cleaning and/or treatment compositions comprising a xyloglucan conjugate |
US20120108488A1 (en) * | 2010-10-29 | 2012-05-03 | Neil Joseph Lant | Cleaning And/Or Treatment Compositions |
-
2014
- 2014-11-12 DE DE102014016675.9A patent/DE102014016675B4/de active Active
-
2015
- 2015-11-11 PL PL15194014T patent/PL3020794T3/pl unknown
- 2015-11-11 EP EP15194014.5A patent/EP3020794B1/fr active Active
Non-Patent Citations (1)
Title |
---|
None |
Also Published As
Publication number | Publication date |
---|---|
EP3020794A3 (fr) | 2016-06-08 |
EP3020794B1 (fr) | 2020-02-19 |
DE102014016675A1 (de) | 2016-05-12 |
DE102014016675B4 (de) | 2022-02-24 |
PL3020794T3 (pl) | 2020-10-19 |
Similar Documents
Publication | Publication Date | Title |
---|---|---|
WO2007087953A1 (fr) | Agent de nettoyage ou de lavage comportant un inhibiteur de transfert de colorant | |
WO2011117079A1 (fr) | Agents de lavage, nettoyage ou prétraitement à pouvoir dégraissant renforcé | |
DE102014206064A1 (de) | Flüssigwaschmittel enthaltend Polymere zur Verstärkung der Duftstoffleistung | |
WO2013107579A1 (fr) | Détergent, produit de nettoyage ou agent de prétraitement présentant une force de nettoyage augmentée | |
WO2013186170A1 (fr) | Agents de lavage, de nettoyage ou de pré-traitement à pouvoir nettoyant renforcé | |
WO2008155160A1 (fr) | Lessives ou détergents liquides hautement moussants, présentant une viscosité stable | |
EP1268730B1 (fr) | Produit d'entretien pour le textile | |
EP3020794B1 (fr) | Composition de lessive et son utilisation | |
EP2414496B1 (fr) | Composition d'agent de blanchiment liquide | |
EP3116984A1 (fr) | Mélange de tensioactifs amélioré ayant un degré d'éthoxylation optimisé | |
DE102006034902A1 (de) | Wasch- oder Reinigungsmittel mit verbessertem Dispergievermögen | |
WO2017050821A1 (fr) | Composition contenant des tensioactifs pour le traitement de textiles avec un colorant | |
WO1999060087A1 (fr) | Agent de blanchiment aqueux | |
DE19961662A1 (de) | PIT-Dispersionen von duftaktiven Wachsen | |
EP3450532B1 (fr) | Utilisation d'un copolymère amodiméthicone / organosilicium, détergent, utilisation du détergent et procédé de lavage | |
EP2108038B1 (fr) | Lessive ou détergent à viscosité stable | |
WO2014195215A1 (fr) | Agents de lavage, de nettoyage ou de pré-traitement à pouvoir nettoyant iii renforcé | |
WO1998005750A1 (fr) | Procede de lavage | |
DE10253109A1 (de) | Wäßriges Bleichmittel | |
WO2015091054A1 (fr) | Systèmes de michael pour la stabilisation d'une matière odoriférante | |
EP0893490A2 (fr) | Composition adoucissante pour tissus sans azote | |
EP2723843B1 (fr) | Utilisation des produits de lavage ou de nettoyage à pouvoir nettoyant accru | |
DE102004017112B4 (de) | Verwendung von Pudermittel | |
WO2014195216A1 (fr) | Agents de lavage, de nettoyage ou de pré-traitement à pouvoir nettoyant iv renforcé | |
DE19846439A1 (de) | Waschmittel mit kationischen Alkyl- und/oder Alkenylpolyglykosiden |
Legal Events
Date | Code | Title | Description |
---|---|---|---|
REG | Reference to a national code |
Ref country code: DE Ref legal event code: R079 Ref document number: 502015011764 Country of ref document: DE Free format text: PREVIOUS MAIN CLASS: C11D0003000000 Ipc: C11D0003400000 |
|
PUAL | Search report despatched |
Free format text: ORIGINAL CODE: 0009013 |
|
PUAI | Public reference made under article 153(3) epc to a published international application that has entered the european phase |
Free format text: ORIGINAL CODE: 0009012 |
|
AK | Designated contracting states |
Kind code of ref document: A2 Designated state(s): AL AT BE BG CH CY CZ DE DK EE ES FI FR GB GR HR HU IE IS IT LI LT LU LV MC MK MT NL NO PL PT RO RS SE SI SK SM TR |
|
AX | Request for extension of the european patent |
Extension state: BA ME |
|
AK | Designated contracting states |
Kind code of ref document: A3 Designated state(s): AL AT BE BG CH CY CZ DE DK EE ES FI FR GB GR HR HU IE IS IT LI LT LU LV MC MK MT NL NO PL PT RO RS SE SI SK SM TR |
|
AX | Request for extension of the european patent |
Extension state: BA ME |
|
RIC1 | Information provided on ipc code assigned before grant |
Ipc: C11D 3/40 20060101AFI20160429BHEP |
|
STAA | Information on the status of an ep patent application or granted ep patent |
Free format text: STATUS: REQUEST FOR EXAMINATION WAS MADE |
|
17P | Request for examination filed |
Effective date: 20161207 |
|
RBV | Designated contracting states (corrected) |
Designated state(s): AL AT BE BG CH CY CZ DE DK EE ES FI FR GB GR HR HU IE IS IT LI LT LU LV MC MK MT NL NO PL PT RO RS SE SI SK SM TR |
|
STAA | Information on the status of an ep patent application or granted ep patent |
Free format text: STATUS: EXAMINATION IS IN PROGRESS |
|
17Q | First examination report despatched |
Effective date: 20180212 |
|
GRAP | Despatch of communication of intention to grant a patent |
Free format text: ORIGINAL CODE: EPIDOSNIGR1 |
|
STAA | Information on the status of an ep patent application or granted ep patent |
Free format text: STATUS: GRANT OF PATENT IS INTENDED |
|
INTG | Intention to grant announced |
Effective date: 20191029 |
|
GRAS | Grant fee paid |
Free format text: ORIGINAL CODE: EPIDOSNIGR3 |
|
GRAA | (expected) grant |
Free format text: ORIGINAL CODE: 0009210 |
|
STAA | Information on the status of an ep patent application or granted ep patent |
Free format text: STATUS: THE PATENT HAS BEEN GRANTED |
|
AK | Designated contracting states |
Kind code of ref document: B1 Designated state(s): AL AT BE BG CH CY CZ DE DK EE ES FI FR GB GR HR HU IE IS IT LI LT LU LV MC MK MT NL NO PL PT RO RS SE SI SK SM TR |
|
REG | Reference to a national code |
Ref country code: CH Ref legal event code: EP |
|
REG | Reference to a national code |
Ref country code: DE Ref legal event code: R096 Ref document number: 502015011764 Country of ref document: DE |
|
REG | Reference to a national code |
Ref country code: AT Ref legal event code: REF Ref document number: 1234973 Country of ref document: AT Kind code of ref document: T Effective date: 20200315 |
|
REG | Reference to a national code |
Ref country code: IE Ref legal event code: FG4D Free format text: LANGUAGE OF EP DOCUMENT: GERMAN |
|
REG | Reference to a national code |
Ref country code: CH Ref legal event code: NV Representative=s name: WEINMANN ZIMMERLI, CH |
|
REG | Reference to a national code |
Ref country code: NL Ref legal event code: MP Effective date: 20200219 |
|
PG25 | Lapsed in a contracting state [announced via postgrant information from national office to epo] |
Ref country code: NO Free format text: LAPSE BECAUSE OF FAILURE TO SUBMIT A TRANSLATION OF THE DESCRIPTION OR TO PAY THE FEE WITHIN THE PRESCRIBED TIME-LIMIT Effective date: 20200519 Ref country code: FI Free format text: LAPSE BECAUSE OF FAILURE TO SUBMIT A TRANSLATION OF THE DESCRIPTION OR TO PAY THE FEE WITHIN THE PRESCRIBED TIME-LIMIT Effective date: 20200219 Ref country code: RS Free format text: LAPSE BECAUSE OF FAILURE TO SUBMIT A TRANSLATION OF THE DESCRIPTION OR TO PAY THE FEE WITHIN THE PRESCRIBED TIME-LIMIT Effective date: 20200219 |
|
REG | Reference to a national code |
Ref country code: LT Ref legal event code: MG4D |
|
PG25 | Lapsed in a contracting state [announced via postgrant information from national office to epo] |
Ref country code: HR Free format text: LAPSE BECAUSE OF FAILURE TO SUBMIT A TRANSLATION OF THE DESCRIPTION OR TO PAY THE FEE WITHIN THE PRESCRIBED TIME-LIMIT Effective date: 20200219 Ref country code: LV Free format text: LAPSE BECAUSE OF FAILURE TO SUBMIT A TRANSLATION OF THE DESCRIPTION OR TO PAY THE FEE WITHIN THE PRESCRIBED TIME-LIMIT Effective date: 20200219 Ref country code: SE Free format text: LAPSE BECAUSE OF FAILURE TO SUBMIT A TRANSLATION OF THE DESCRIPTION OR TO PAY THE FEE WITHIN THE PRESCRIBED TIME-LIMIT Effective date: 20200219 Ref country code: GR Free format text: LAPSE BECAUSE OF FAILURE TO SUBMIT A TRANSLATION OF THE DESCRIPTION OR TO PAY THE FEE WITHIN THE PRESCRIBED TIME-LIMIT Effective date: 20200520 Ref country code: BG Free format text: LAPSE BECAUSE OF FAILURE TO SUBMIT A TRANSLATION OF THE DESCRIPTION OR TO PAY THE FEE WITHIN THE PRESCRIBED TIME-LIMIT Effective date: 20200519 Ref country code: IS Free format text: LAPSE BECAUSE OF FAILURE TO SUBMIT A TRANSLATION OF THE DESCRIPTION OR TO PAY THE FEE WITHIN THE PRESCRIBED TIME-LIMIT Effective date: 20200619 |
|
PG25 | Lapsed in a contracting state [announced via postgrant information from national office to epo] |
Ref country code: NL Free format text: LAPSE BECAUSE OF FAILURE TO SUBMIT A TRANSLATION OF THE DESCRIPTION OR TO PAY THE FEE WITHIN THE PRESCRIBED TIME-LIMIT Effective date: 20200219 |
|
PG25 | Lapsed in a contracting state [announced via postgrant information from national office to epo] |
Ref country code: PT Free format text: LAPSE BECAUSE OF FAILURE TO SUBMIT A TRANSLATION OF THE DESCRIPTION OR TO PAY THE FEE WITHIN THE PRESCRIBED TIME-LIMIT Effective date: 20200712 Ref country code: SK Free format text: LAPSE BECAUSE OF FAILURE TO SUBMIT A TRANSLATION OF THE DESCRIPTION OR TO PAY THE FEE WITHIN THE PRESCRIBED TIME-LIMIT Effective date: 20200219 Ref country code: DK Free format text: LAPSE BECAUSE OF FAILURE TO SUBMIT A TRANSLATION OF THE DESCRIPTION OR TO PAY THE FEE WITHIN THE PRESCRIBED TIME-LIMIT Effective date: 20200219 Ref country code: EE Free format text: LAPSE BECAUSE OF FAILURE TO SUBMIT A TRANSLATION OF THE DESCRIPTION OR TO PAY THE FEE WITHIN THE PRESCRIBED TIME-LIMIT Effective date: 20200219 Ref country code: SM Free format text: LAPSE BECAUSE OF FAILURE TO SUBMIT A TRANSLATION OF THE DESCRIPTION OR TO PAY THE FEE WITHIN THE PRESCRIBED TIME-LIMIT Effective date: 20200219 Ref country code: ES Free format text: LAPSE BECAUSE OF FAILURE TO SUBMIT A TRANSLATION OF THE DESCRIPTION OR TO PAY THE FEE WITHIN THE PRESCRIBED TIME-LIMIT Effective date: 20200219 Ref country code: LT Free format text: LAPSE BECAUSE OF FAILURE TO SUBMIT A TRANSLATION OF THE DESCRIPTION OR TO PAY THE FEE WITHIN THE PRESCRIBED TIME-LIMIT Effective date: 20200219 Ref country code: CZ Free format text: LAPSE BECAUSE OF FAILURE TO SUBMIT A TRANSLATION OF THE DESCRIPTION OR TO PAY THE FEE WITHIN THE PRESCRIBED TIME-LIMIT Effective date: 20200219 Ref country code: RO Free format text: LAPSE BECAUSE OF FAILURE TO SUBMIT A TRANSLATION OF THE DESCRIPTION OR TO PAY THE FEE WITHIN THE PRESCRIBED TIME-LIMIT Effective date: 20200219 |
|
REG | Reference to a national code |
Ref country code: DE Ref legal event code: R097 Ref document number: 502015011764 Country of ref document: DE |
|
PLBE | No opposition filed within time limit |
Free format text: ORIGINAL CODE: 0009261 |
|
STAA | Information on the status of an ep patent application or granted ep patent |
Free format text: STATUS: NO OPPOSITION FILED WITHIN TIME LIMIT |
|
26N | No opposition filed |
Effective date: 20201120 |
|
PG25 | Lapsed in a contracting state [announced via postgrant information from national office to epo] |
Ref country code: IT Free format text: LAPSE BECAUSE OF FAILURE TO SUBMIT A TRANSLATION OF THE DESCRIPTION OR TO PAY THE FEE WITHIN THE PRESCRIBED TIME-LIMIT Effective date: 20200219 |
|
PG25 | Lapsed in a contracting state [announced via postgrant information from national office to epo] |
Ref country code: SI Free format text: LAPSE BECAUSE OF FAILURE TO SUBMIT A TRANSLATION OF THE DESCRIPTION OR TO PAY THE FEE WITHIN THE PRESCRIBED TIME-LIMIT Effective date: 20200219 |
|
PG25 | Lapsed in a contracting state [announced via postgrant information from national office to epo] |
Ref country code: MC Free format text: LAPSE BECAUSE OF FAILURE TO SUBMIT A TRANSLATION OF THE DESCRIPTION OR TO PAY THE FEE WITHIN THE PRESCRIBED TIME-LIMIT Effective date: 20200219 |
|
PG25 | Lapsed in a contracting state [announced via postgrant information from national office to epo] |
Ref country code: LU Free format text: LAPSE BECAUSE OF NON-PAYMENT OF DUE FEES Effective date: 20201111 |
|
REG | Reference to a national code |
Ref country code: BE Ref legal event code: MM Effective date: 20201130 |
|
PG25 | Lapsed in a contracting state [announced via postgrant information from national office to epo] |
Ref country code: IE Free format text: LAPSE BECAUSE OF NON-PAYMENT OF DUE FEES Effective date: 20201111 |
|
PG25 | Lapsed in a contracting state [announced via postgrant information from national office to epo] |
Ref country code: TR Free format text: LAPSE BECAUSE OF FAILURE TO SUBMIT A TRANSLATION OF THE DESCRIPTION OR TO PAY THE FEE WITHIN THE PRESCRIBED TIME-LIMIT Effective date: 20200219 Ref country code: MT Free format text: LAPSE BECAUSE OF FAILURE TO SUBMIT A TRANSLATION OF THE DESCRIPTION OR TO PAY THE FEE WITHIN THE PRESCRIBED TIME-LIMIT Effective date: 20200219 Ref country code: CY Free format text: LAPSE BECAUSE OF FAILURE TO SUBMIT A TRANSLATION OF THE DESCRIPTION OR TO PAY THE FEE WITHIN THE PRESCRIBED TIME-LIMIT Effective date: 20200219 |
|
PG25 | Lapsed in a contracting state [announced via postgrant information from national office to epo] |
Ref country code: MK Free format text: LAPSE BECAUSE OF FAILURE TO SUBMIT A TRANSLATION OF THE DESCRIPTION OR TO PAY THE FEE WITHIN THE PRESCRIBED TIME-LIMIT Effective date: 20200219 Ref country code: AL Free format text: LAPSE BECAUSE OF FAILURE TO SUBMIT A TRANSLATION OF THE DESCRIPTION OR TO PAY THE FEE WITHIN THE PRESCRIBED TIME-LIMIT Effective date: 20200219 |
|
PG25 | Lapsed in a contracting state [announced via postgrant information from national office to epo] |
Ref country code: BE Free format text: LAPSE BECAUSE OF NON-PAYMENT OF DUE FEES Effective date: 20201130 |
|
P01 | Opt-out of the competence of the unified patent court (upc) registered |
Effective date: 20230528 |
|
PGFP | Annual fee paid to national office [announced via postgrant information from national office to epo] |
Ref country code: GB Payment date: 20231123 Year of fee payment: 9 |
|
PGFP | Annual fee paid to national office [announced via postgrant information from national office to epo] |
Ref country code: FR Payment date: 20231123 Year of fee payment: 9 Ref country code: DE Payment date: 20231128 Year of fee payment: 9 Ref country code: CH Payment date: 20231201 Year of fee payment: 9 Ref country code: AT Payment date: 20231117 Year of fee payment: 9 |
|
PGFP | Annual fee paid to national office [announced via postgrant information from national office to epo] |
Ref country code: PL Payment date: 20231027 Year of fee payment: 9 |