CA2414140C - Automatic dishwashing method employing an organic solvent system - Google Patents
Automatic dishwashing method employing an organic solvent system Download PDFInfo
- Publication number
- CA2414140C CA2414140C CA002414140A CA2414140A CA2414140C CA 2414140 C CA2414140 C CA 2414140C CA 002414140 A CA002414140 A CA 002414140A CA 2414140 A CA2414140 A CA 2414140A CA 2414140 C CA2414140 C CA 2414140C
- Authority
- CA
- Canada
- Prior art keywords
- organic solvent
- automatic dishwashing
- composition
- solvent
- compositions
- 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.)
- Expired - Lifetime
Links
- 238000004851 dishwashing Methods 0.000 title claims abstract description 142
- 239000003960 organic solvent Substances 0.000 title claims abstract description 120
- 238000000034 method Methods 0.000 title claims abstract description 73
- 239000000203 mixture Substances 0.000 claims abstract description 297
- 239000002904 solvent Substances 0.000 claims abstract description 129
- 239000003599 detergent Substances 0.000 claims abstract description 93
- 239000002689 soil Substances 0.000 claims abstract description 50
- 238000003860 storage Methods 0.000 claims abstract description 16
- 238000005406 washing Methods 0.000 claims abstract description 11
- -1 glycol ethers Chemical class 0.000 claims description 34
- 239000004094 surface-active agent Substances 0.000 claims description 32
- 239000007788 liquid Substances 0.000 claims description 31
- 235000013305 food Nutrition 0.000 claims description 25
- MTHSVFCYNBDYFN-UHFFFAOYSA-N diethylene glycol Chemical compound OCCOCCO MTHSVFCYNBDYFN-UHFFFAOYSA-N 0.000 claims description 16
- 239000000499 gel Substances 0.000 claims description 13
- 239000001257 hydrogen Substances 0.000 claims description 13
- 229910052739 hydrogen Inorganic materials 0.000 claims description 13
- 239000000080 wetting agent Substances 0.000 claims description 13
- LYCAIKOWRPUZTN-UHFFFAOYSA-N ethylene glycol Natural products OCCO LYCAIKOWRPUZTN-UHFFFAOYSA-N 0.000 claims description 10
- 150000002334 glycols Chemical class 0.000 claims description 10
- 230000007480 spreading Effects 0.000 claims description 9
- 238000003892 spreading Methods 0.000 claims description 9
- 239000000758 substrate Substances 0.000 claims description 8
- RWNUSVWFHDHRCJ-UHFFFAOYSA-N 1-butoxypropan-2-ol Chemical compound CCCCOCC(C)O RWNUSVWFHDHRCJ-UHFFFAOYSA-N 0.000 claims description 7
- 150000001298 alcohols Chemical class 0.000 claims description 7
- 150000001412 amines Chemical class 0.000 claims description 6
- 239000004519 grease Substances 0.000 claims description 6
- SBASXUCJHJRPEV-UHFFFAOYSA-N 2-(2-methoxyethoxy)ethanol Chemical compound COCCOCCO SBASXUCJHJRPEV-UHFFFAOYSA-N 0.000 claims description 5
- HZAXFHJVJLSVMW-UHFFFAOYSA-N 2-Aminoethan-1-ol Chemical group NCCO HZAXFHJVJLSVMW-UHFFFAOYSA-N 0.000 claims description 5
- 229940028356 diethylene glycol monobutyl ether Drugs 0.000 claims description 5
- JCGNDDUYTRNOFT-UHFFFAOYSA-N oxolane-2,4-dione Chemical compound O=C1COC(=O)C1 JCGNDDUYTRNOFT-UHFFFAOYSA-N 0.000 claims description 5
- 239000006072 paste Substances 0.000 claims description 5
- XNWFRZJHXBZDAG-UHFFFAOYSA-N 2-METHOXYETHANOL Chemical compound COCCO XNWFRZJHXBZDAG-UHFFFAOYSA-N 0.000 claims description 4
- POAOYUHQDCAZBD-UHFFFAOYSA-N 2-butoxyethanol Chemical group CCCCOCCO POAOYUHQDCAZBD-UHFFFAOYSA-N 0.000 claims description 4
- ZNQVEEAIQZEUHB-UHFFFAOYSA-N 2-ethoxyethanol Chemical compound CCOCCO ZNQVEEAIQZEUHB-UHFFFAOYSA-N 0.000 claims description 4
- RTZKZFJDLAIYFH-UHFFFAOYSA-N Diethyl ether Chemical class CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 claims description 4
- 239000004721 Polyphenylene oxide Substances 0.000 claims description 4
- 239000006071 cream Substances 0.000 claims description 4
- 230000003111 delayed effect Effects 0.000 claims description 4
- 239000011521 glass Substances 0.000 claims description 4
- WGCNASOHLSPBMP-UHFFFAOYSA-N hydroxyacetaldehyde Natural products OCC=O WGCNASOHLSPBMP-UHFFFAOYSA-N 0.000 claims description 4
- 239000012046 mixed solvent Substances 0.000 claims description 4
- 229920000570 polyether Polymers 0.000 claims description 4
- OPKOKAMJFNKNAS-UHFFFAOYSA-N N-methylethanolamine Chemical compound CNCCO OPKOKAMJFNKNAS-UHFFFAOYSA-N 0.000 claims description 3
- 230000001476 alcoholic effect Effects 0.000 claims description 3
- 238000009835 boiling Methods 0.000 claims description 3
- XXJWXESWEXIICW-UHFFFAOYSA-N diethylene glycol monoethyl ether Chemical compound CCOCCOCCO XXJWXESWEXIICW-UHFFFAOYSA-N 0.000 claims description 3
- 229940075557 diethylene glycol monoethyl ether Drugs 0.000 claims description 3
- 150000002148 esters Chemical class 0.000 claims description 3
- 239000012454 non-polar solvent Substances 0.000 claims description 3
- 229920001296 polysiloxane Polymers 0.000 claims description 3
- HXKKHQJGJAFBHI-UHFFFAOYSA-N 1-aminopropan-2-ol Chemical compound CC(O)CN HXKKHQJGJAFBHI-UHFFFAOYSA-N 0.000 claims description 2
- BFSVOASYOCHEOV-UHFFFAOYSA-N 2-diethylaminoethanol Chemical compound CCN(CC)CCO BFSVOASYOCHEOV-UHFFFAOYSA-N 0.000 claims description 2
- AKNUHUCEWALCOI-UHFFFAOYSA-N N-ethyldiethanolamine Chemical compound OCCN(CC)CCO AKNUHUCEWALCOI-UHFFFAOYSA-N 0.000 claims description 2
- GSEJCLTVZPLZKY-UHFFFAOYSA-N Triethanolamine Chemical compound OCCN(CCO)CCO GSEJCLTVZPLZKY-UHFFFAOYSA-N 0.000 claims description 2
- 150000003863 ammonium salts Chemical class 0.000 claims description 2
- 239000012876 carrier material Substances 0.000 claims description 2
- ZBCBWPMODOFKDW-UHFFFAOYSA-N diethanolamine Chemical compound OCCNCCO ZBCBWPMODOFKDW-UHFFFAOYSA-N 0.000 claims description 2
- 238000002156 mixing Methods 0.000 claims description 2
- 230000002459 sustained effect Effects 0.000 claims description 2
- 150000003505 terpenes Chemical class 0.000 claims description 2
- 235000007586 terpenes Nutrition 0.000 claims description 2
- 230000001960 triggered effect Effects 0.000 claims description 2
- CUVLMZNMSPJDON-UHFFFAOYSA-N 1-(1-butoxypropan-2-yloxy)propan-2-ol Chemical compound CCCCOCC(C)OCC(C)O CUVLMZNMSPJDON-UHFFFAOYSA-N 0.000 claims 2
- QCDWFXQBSFUVSP-UHFFFAOYSA-N 2-phenoxyethanol Chemical compound OCCOC1=CC=CC=C1 QCDWFXQBSFUVSP-UHFFFAOYSA-N 0.000 claims 2
- DURPTKYDGMDSBL-UHFFFAOYSA-N 1-butoxybutane Chemical compound CCCCOCCCC DURPTKYDGMDSBL-UHFFFAOYSA-N 0.000 claims 1
- 230000008569 process Effects 0.000 abstract description 5
- 239000002736 nonionic surfactant Substances 0.000 description 22
- 229920002125 Sokalan® Polymers 0.000 description 20
- KWYUFKZDYYNOTN-UHFFFAOYSA-M Potassium hydroxide Chemical compound [OH-].[K+] KWYUFKZDYYNOTN-UHFFFAOYSA-M 0.000 description 18
- DNIAPMSPPWPWGF-UHFFFAOYSA-N Propylene glycol Chemical compound CC(O)CO DNIAPMSPPWPWGF-UHFFFAOYSA-N 0.000 description 16
- 239000007844 bleaching agent Substances 0.000 description 16
- 238000005187 foaming Methods 0.000 description 14
- 239000002562 thickening agent Substances 0.000 description 14
- 238000004140 cleaning Methods 0.000 description 13
- 229920000642 polymer Polymers 0.000 description 12
- 235000019832 sodium triphosphate Nutrition 0.000 description 12
- 108090000790 Enzymes Proteins 0.000 description 10
- 102000004190 Enzymes Human genes 0.000 description 10
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 10
- 229940088598 enzyme Drugs 0.000 description 9
- 239000000463 material Substances 0.000 description 9
- 239000002243 precursor Substances 0.000 description 8
- 235000013772 propylene glycol Nutrition 0.000 description 8
- 125000000217 alkyl group Chemical group 0.000 description 7
- 125000004432 carbon atom Chemical group C* 0.000 description 7
- BPQQTUXANYXVAA-UHFFFAOYSA-N Orthosilicate Chemical compound [O-][Si]([O-])([O-])[O-] BPQQTUXANYXVAA-UHFFFAOYSA-N 0.000 description 6
- 101710194948 Protein phosphatase PhpP Proteins 0.000 description 6
- 150000001875 compounds Chemical class 0.000 description 6
- HWGNBUXHKFFFIH-UHFFFAOYSA-I pentasodium;[oxido(phosphonatooxy)phosphoryl] phosphate Chemical compound [Na+].[Na+].[Na+].[Na+].[Na+].[O-]P([O-])(=O)OP([O-])(=O)OP([O-])([O-])=O HWGNBUXHKFFFIH-UHFFFAOYSA-I 0.000 description 6
- 229920005862 polyol Polymers 0.000 description 6
- 150000003077 polyols Chemical class 0.000 description 6
- 150000003839 salts Chemical class 0.000 description 6
- 239000003826 tablet Substances 0.000 description 6
- 108010075550 termamyl Proteins 0.000 description 6
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 5
- QAOWNCQODCNURD-UHFFFAOYSA-N Sulfuric acid Chemical compound OS(O)(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-N 0.000 description 5
- CBTVGIZVANVGBH-UHFFFAOYSA-N aminomethyl propanol Chemical compound CC(C)(N)CO CBTVGIZVANVGBH-UHFFFAOYSA-N 0.000 description 5
- DMSMPAJRVJJAGA-UHFFFAOYSA-N benzo[d]isothiazol-3-one Chemical compound C1=CC=C2C(=O)NSC2=C1 DMSMPAJRVJJAGA-UHFFFAOYSA-N 0.000 description 5
- KRKNYBCHXYNGOX-UHFFFAOYSA-N citric acid Chemical compound OC(=O)CC(O)(C(O)=O)CC(O)=O KRKNYBCHXYNGOX-UHFFFAOYSA-N 0.000 description 5
- 229920001577 copolymer Polymers 0.000 description 5
- 239000002304 perfume Substances 0.000 description 5
- 235000011149 sulphuric acid Nutrition 0.000 description 5
- DNIAPMSPPWPWGF-GSVOUGTGSA-N (R)-(-)-Propylene glycol Chemical compound C[C@@H](O)CO DNIAPMSPPWPWGF-GSVOUGTGSA-N 0.000 description 4
- NIXOWILDQLNWCW-UHFFFAOYSA-N 2-Propenoic acid Natural products OC(=O)C=C NIXOWILDQLNWCW-UHFFFAOYSA-N 0.000 description 4
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 description 4
- 239000004115 Sodium Silicate Substances 0.000 description 4
- CZMRCDWAGMRECN-UGDNZRGBSA-N Sucrose Chemical compound O[C@H]1[C@H](O)[C@@H](CO)O[C@@]1(CO)O[C@@H]1[C@H](O)[C@@H](O)[C@H](O)[C@@H](CO)O1 CZMRCDWAGMRECN-UGDNZRGBSA-N 0.000 description 4
- 229930006000 Sucrose Natural products 0.000 description 4
- 150000003973 alkyl amines Chemical class 0.000 description 4
- QRUDEWIWKLJBPS-UHFFFAOYSA-N benzotriazole Chemical compound C1=CC=C2N[N][N]C2=C1 QRUDEWIWKLJBPS-UHFFFAOYSA-N 0.000 description 4
- KGBXLFKZBHKPEV-UHFFFAOYSA-N boric acid Chemical compound OB(O)O KGBXLFKZBHKPEV-UHFFFAOYSA-N 0.000 description 4
- 239000004327 boric acid Substances 0.000 description 4
- 239000003795 chemical substances by application Substances 0.000 description 4
- 239000004927 clay Substances 0.000 description 4
- 239000008187 granular material Substances 0.000 description 4
- 229930195733 hydrocarbon Natural products 0.000 description 4
- 239000011572 manganese Substances 0.000 description 4
- 239000003921 oil Substances 0.000 description 4
- 235000019198 oils Nutrition 0.000 description 4
- 239000002245 particle Substances 0.000 description 4
- 229920005646 polycarboxylate Polymers 0.000 description 4
- 239000011734 sodium Substances 0.000 description 4
- 239000010935 stainless steel Substances 0.000 description 4
- 229910001220 stainless steel Inorganic materials 0.000 description 4
- 239000005720 sucrose Substances 0.000 description 4
- SMZOUWXMTYCWNB-UHFFFAOYSA-N 2-(2-methoxy-5-methylphenyl)ethanamine Chemical compound COC1=CC=C(C)C=C1CCN SMZOUWXMTYCWNB-UHFFFAOYSA-N 0.000 description 3
- WVDDGKGOMKODPV-UHFFFAOYSA-N Benzyl alcohol Chemical compound OCC1=CC=CC=C1 WVDDGKGOMKODPV-UHFFFAOYSA-N 0.000 description 3
- 239000004215 Carbon black (E152) Substances 0.000 description 3
- BVKZGUZCCUSVTD-UHFFFAOYSA-L Carbonate Chemical compound [O-]C([O-])=O BVKZGUZCCUSVTD-UHFFFAOYSA-L 0.000 description 3
- XEKOWRVHYACXOJ-UHFFFAOYSA-N Ethyl acetate Chemical compound CCOC(C)=O XEKOWRVHYACXOJ-UHFFFAOYSA-N 0.000 description 3
- DBVJJBKOTRCVKF-UHFFFAOYSA-N Etidronic acid Chemical compound OP(=O)(O)C(O)(C)P(O)(O)=O DBVJJBKOTRCVKF-UHFFFAOYSA-N 0.000 description 3
- PEDCQBHIVMGVHV-UHFFFAOYSA-N Glycerine Chemical compound OCC(O)CO PEDCQBHIVMGVHV-UHFFFAOYSA-N 0.000 description 3
- OKKJLVBELUTLKV-UHFFFAOYSA-N Methanol Chemical compound OC OKKJLVBELUTLKV-UHFFFAOYSA-N 0.000 description 3
- TTZMPOZCBFTTPR-UHFFFAOYSA-N O=P1OCO1 Chemical compound O=P1OCO1 TTZMPOZCBFTTPR-UHFFFAOYSA-N 0.000 description 3
- 108091005804 Peptidases Proteins 0.000 description 3
- 229920001030 Polyethylene Glycol 4000 Polymers 0.000 description 3
- 239000004365 Protease Substances 0.000 description 3
- YIMQCDZDWXUDCA-UHFFFAOYSA-N [4-(hydroxymethyl)cyclohexyl]methanol Chemical compound OCC1CCC(CO)CC1 YIMQCDZDWXUDCA-UHFFFAOYSA-N 0.000 description 3
- 125000002947 alkylene group Chemical group 0.000 description 3
- WPYMKLBDIGXBTP-UHFFFAOYSA-N benzoic acid Chemical compound OC(=O)C1=CC=CC=C1 WPYMKLBDIGXBTP-UHFFFAOYSA-N 0.000 description 3
- 239000000460 chlorine Substances 0.000 description 3
- 238000005260 corrosion Methods 0.000 description 3
- XPFVYQJUAUNWIW-UHFFFAOYSA-N furfuryl alcohol Chemical compound OCC1=CC=CO1 XPFVYQJUAUNWIW-UHFFFAOYSA-N 0.000 description 3
- 229940094522 laponite Drugs 0.000 description 3
- XCOBTUNSZUJCDH-UHFFFAOYSA-B lithium magnesium sodium silicate Chemical compound [Li+].[Li+].[OH-].[OH-].[OH-].[OH-].[OH-].[OH-].[OH-].[OH-].[OH-].[OH-].[OH-].[OH-].[Na+].[Na+].[Mg+2].[Mg+2].[Mg+2].[Mg+2].[Mg+2].[Mg+2].[Mg+2].[Mg+2].[Mg+2].[Mg+2].[Mg+2].[Mg+2].[Mg+2].[Mg+2].[Mg+2].[Mg+2].O1[Si](O2)([O-])O[Si]3([O-])O[Si]1([O-])O[Si]2([O-])O3.O1[Si](O2)([O-])O[Si]3([O-])O[Si]1([O-])O[Si]2([O-])O3.O1[Si](O2)([O-])O[Si]3([O-])O[Si]1([O-])O[Si]2([O-])O3.O1[Si](O2)([O-])O[Si]3([O-])O[Si]1([O-])O[Si]2([O-])O3.O1[Si](O2)([O-])O[Si]3([O-])O[Si]1([O-])O[Si]2([O-])O3.O1[Si](O2)([O-])O[Si]3([O-])O[Si]1([O-])O[Si]2([O-])O3 XCOBTUNSZUJCDH-UHFFFAOYSA-B 0.000 description 3
- 150000004967 organic peroxy acids Chemical class 0.000 description 3
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- 239000000843 powder Substances 0.000 description 3
- 150000003138 primary alcohols Chemical class 0.000 description 3
- NTHWMYGWWRZVTN-UHFFFAOYSA-N sodium silicate Chemical compound [Na+].[Na+].[O-][Si]([O-])=O NTHWMYGWWRZVTN-UHFFFAOYSA-N 0.000 description 3
- 229910052911 sodium silicate Inorganic materials 0.000 description 3
- UNXRWKVEANCORM-UHFFFAOYSA-I triphosphate(5-) Chemical compound [O-]P([O-])(=O)OP([O-])(=O)OP([O-])([O-])=O UNXRWKVEANCORM-UHFFFAOYSA-I 0.000 description 3
- JVTIXNMXDLQEJE-UHFFFAOYSA-N 2-decanoyloxypropyl decanoate 2-octanoyloxypropyl octanoate Chemical compound C(CCCCCCC)(=O)OCC(C)OC(CCCCCCC)=O.C(=O)(CCCCCCCCC)OCC(C)OC(=O)CCCCCCCCC JVTIXNMXDLQEJE-UHFFFAOYSA-N 0.000 description 2
- YNJSNEKCXVFDKW-UHFFFAOYSA-N 3-(5-amino-1h-indol-3-yl)-2-azaniumylpropanoate Chemical compound C1=C(N)C=C2C(CC(N)C(O)=O)=CNC2=C1 YNJSNEKCXVFDKW-UHFFFAOYSA-N 0.000 description 2
- ATVJXMYDOSMEPO-UHFFFAOYSA-N 3-prop-2-enoxyprop-1-ene Chemical group C=CCOCC=C ATVJXMYDOSMEPO-UHFFFAOYSA-N 0.000 description 2
- XSVSPKKXQGNHMD-UHFFFAOYSA-N 5-bromo-3-methyl-1,2-thiazole Chemical compound CC=1C=C(Br)SN=1 XSVSPKKXQGNHMD-UHFFFAOYSA-N 0.000 description 2
- 239000004382 Amylase Substances 0.000 description 2
- GAWIXWVDTYZWAW-UHFFFAOYSA-N C[CH]O Chemical group C[CH]O GAWIXWVDTYZWAW-UHFFFAOYSA-N 0.000 description 2
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 description 2
- ZAMOUSCENKQFHK-UHFFFAOYSA-N Chlorine atom Chemical compound [Cl] ZAMOUSCENKQFHK-UHFFFAOYSA-N 0.000 description 2
- ROSDSFDQCJNGOL-UHFFFAOYSA-N Dimethylamine Chemical compound CNC ROSDSFDQCJNGOL-UHFFFAOYSA-N 0.000 description 2
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- 102100037486 Reverse transcriptase/ribonuclease H Human genes 0.000 description 2
- UIIMBOGNXHQVGW-UHFFFAOYSA-M Sodium bicarbonate Chemical compound [Na+].OC([O-])=O UIIMBOGNXHQVGW-UHFFFAOYSA-M 0.000 description 2
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- 125000003277 amino group Chemical group 0.000 description 2
- 239000012964 benzotriazole Substances 0.000 description 2
- 239000002775 capsule Substances 0.000 description 2
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- 239000002270 dispersing agent Substances 0.000 description 2
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- NAQMVNRVTILPCV-UHFFFAOYSA-N hexane-1,6-diamine Chemical compound NCCCCCCN NAQMVNRVTILPCV-UHFFFAOYSA-N 0.000 description 2
- 239000003112 inhibitor Substances 0.000 description 2
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- IBOBFGGLRNWLIL-UHFFFAOYSA-N n,n-dimethylhexadecan-1-amine oxide Chemical compound CCCCCCCCCCCCCCCC[N+](C)(C)[O-] IBOBFGGLRNWLIL-UHFFFAOYSA-N 0.000 description 2
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- 235000011176 polyphosphates Nutrition 0.000 description 2
- BITYAPCSNKJESK-UHFFFAOYSA-N potassiosodium Chemical compound [Na].[K] BITYAPCSNKJESK-UHFFFAOYSA-N 0.000 description 2
- 239000011591 potassium Substances 0.000 description 2
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- VXQBJTKSVGFQOL-UHFFFAOYSA-N 2-(2-butoxyethoxy)ethyl acetate Chemical compound CCCCOCCOCCOC(C)=O VXQBJTKSVGFQOL-UHFFFAOYSA-N 0.000 description 1
- FPZWZCWUIYYYBU-UHFFFAOYSA-N 2-(2-ethoxyethoxy)ethyl acetate Chemical compound CCOCCOCCOC(C)=O FPZWZCWUIYYYBU-UHFFFAOYSA-N 0.000 description 1
- BDKLKNJTMLIAFE-UHFFFAOYSA-N 2-(3-fluorophenyl)-1,3-oxazole-4-carbaldehyde Chemical compound FC1=CC=CC(C=2OC=C(C=O)N=2)=C1 BDKLKNJTMLIAFE-UHFFFAOYSA-N 0.000 description 1
- KKMOSYLWYLMHAL-UHFFFAOYSA-N 2-bromo-6-nitroaniline Chemical compound NC1=C(Br)C=CC=C1[N+]([O-])=O KKMOSYLWYLMHAL-UHFFFAOYSA-N 0.000 description 1
- NQBXSWAWVZHKBZ-UHFFFAOYSA-N 2-butoxyethyl acetate Chemical compound CCCCOCCOC(C)=O NQBXSWAWVZHKBZ-UHFFFAOYSA-N 0.000 description 1
- YIWUKEYIRIRTPP-UHFFFAOYSA-N 2-ethylhexan-1-ol Chemical compound CCCCC(CC)CO YIWUKEYIRIRTPP-UHFFFAOYSA-N 0.000 description 1
- RZVAJINKPMORJF-UHFFFAOYSA-N Acetaminophen Chemical compound CC(=O)NC1=CC=C(O)C=C1 RZVAJINKPMORJF-UHFFFAOYSA-N 0.000 description 1
- 239000005995 Aluminium silicate Substances 0.000 description 1
- 108010065511 Amylases Proteins 0.000 description 1
- 102000013142 Amylases Human genes 0.000 description 1
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Classifications
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- C—CHEMISTRY; METALLURGY
- C23—COATING METALLIC MATERIAL; COATING MATERIAL WITH METALLIC MATERIAL; CHEMICAL SURFACE TREATMENT; DIFFUSION TREATMENT OF METALLIC MATERIAL; COATING BY VACUUM EVAPORATION, BY SPUTTERING, BY ION IMPLANTATION OR BY CHEMICAL VAPOUR DEPOSITION, IN GENERAL; INHIBITING CORROSION OF METALLIC MATERIAL OR INCRUSTATION IN GENERAL
- C23G—CLEANING OR DE-GREASING OF METALLIC MATERIAL BY CHEMICAL METHODS OTHER THAN ELECTROLYSIS
- C23G1/00—Cleaning or pickling metallic material with solutions or molten salts
- C23G1/14—Cleaning or pickling metallic material with solutions or molten salts with alkaline solutions
- C23G1/19—Iron or steel
-
- C—CHEMISTRY; METALLURGY
- C11—ANIMAL OR VEGETABLE OILS, FATS, FATTY SUBSTANCES OR WAXES; FATTY ACIDS THEREFROM; DETERGENTS; CANDLES
- C11D—DETERGENT COMPOSITIONS; USE OF SINGLE SUBSTANCES AS DETERGENTS; SOAP OR SOAP-MAKING; RESIN SOAPS; RECOVERY OF GLYCEROL
- C11D17/00—Detergent materials or soaps characterised by their shape or physical properties
- C11D17/0008—Detergent materials or soaps characterised by their shape or physical properties aqueous liquid non soap compositions
- C11D17/003—Colloidal solutions, e.g. gels; Thixotropic solutions or pastes
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- C11—ANIMAL OR VEGETABLE OILS, FATS, FATTY SUBSTANCES OR WAXES; FATTY ACIDS THEREFROM; DETERGENTS; CANDLES
- C11D—DETERGENT COMPOSITIONS; USE OF SINGLE SUBSTANCES AS DETERGENTS; SOAP OR SOAP-MAKING; RESIN SOAPS; RECOVERY OF GLYCEROL
- C11D17/00—Detergent materials or soaps characterised by their shape or physical properties
- C11D17/0043—For use with aerosol devices
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- C11—ANIMAL OR VEGETABLE OILS, FATS, FATTY SUBSTANCES OR WAXES; FATTY ACIDS THEREFROM; DETERGENTS; CANDLES
- C11D—DETERGENT COMPOSITIONS; USE OF SINGLE SUBSTANCES AS DETERGENTS; SOAP OR SOAP-MAKING; RESIN SOAPS; RECOVERY OF GLYCEROL
- C11D17/00—Detergent materials or soaps characterised by their shape or physical properties
- C11D17/04—Detergent materials or soaps characterised by their shape or physical properties combined with or containing other objects
- C11D17/041—Compositions releasably affixed on a substrate or incorporated into a dispensing means
- C11D17/042—Water soluble or water disintegrable containers or substrates containing cleaning compositions or additives for cleaning compositions
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- C11—ANIMAL OR VEGETABLE OILS, FATS, FATTY SUBSTANCES OR WAXES; FATTY ACIDS THEREFROM; DETERGENTS; CANDLES
- C11D—DETERGENT COMPOSITIONS; USE OF SINGLE SUBSTANCES AS DETERGENTS; SOAP OR SOAP-MAKING; RESIN SOAPS; RECOVERY OF GLYCEROL
- C11D3/00—Other compounding ingredients of detergent compositions covered in group C11D1/00
- C11D3/02—Inorganic compounds ; Elemental compounds
- C11D3/12—Water-insoluble compounds
- C11D3/124—Silicon containing, e.g. silica, silex, quartz or glass beads
- C11D3/1246—Silicates, e.g. diatomaceous earth
- C11D3/1253—Layer silicates, e.g. talcum, kaolin, clay, bentonite, smectite, montmorillonite, hectorite or attapulgite
- C11D3/1266—Layer silicates, e.g. talcum, kaolin, clay, bentonite, smectite, montmorillonite, hectorite or attapulgite in liquid compositions
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- C11—ANIMAL OR VEGETABLE OILS, FATS, FATTY SUBSTANCES OR WAXES; FATTY ACIDS THEREFROM; DETERGENTS; CANDLES
- C11D—DETERGENT COMPOSITIONS; USE OF SINGLE SUBSTANCES AS DETERGENTS; SOAP OR SOAP-MAKING; RESIN SOAPS; RECOVERY OF GLYCEROL
- C11D3/00—Other compounding ingredients of detergent compositions covered in group C11D1/00
- C11D3/16—Organic compounds
- C11D3/20—Organic compounds containing oxygen
- C11D3/22—Carbohydrates or derivatives thereof
- C11D3/222—Natural or synthetic polysaccharides, e.g. cellulose, starch, gum, alginic acid or cyclodextrin
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- C11—ANIMAL OR VEGETABLE OILS, FATS, FATTY SUBSTANCES OR WAXES; FATTY ACIDS THEREFROM; DETERGENTS; CANDLES
- C11D—DETERGENT COMPOSITIONS; USE OF SINGLE SUBSTANCES AS DETERGENTS; SOAP OR SOAP-MAKING; RESIN SOAPS; RECOVERY OF GLYCEROL
- C11D3/00—Other compounding ingredients of detergent compositions covered in group C11D1/00
- C11D3/16—Organic compounds
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- C11D3/22—Carbohydrates or derivatives thereof
- C11D3/222—Natural or synthetic polysaccharides, e.g. cellulose, starch, gum, alginic acid or cyclodextrin
- C11D3/225—Natural or synthetic polysaccharides, e.g. cellulose, starch, gum, alginic acid or cyclodextrin etherified, e.g. CMC
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- 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
- C11D3/43—Solvents
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- 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
- C11D3/50—Perfumes
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- 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
- C11D7/00—Compositions of detergents based essentially on non-surface-active compounds
- C11D7/02—Inorganic compounds
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- 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
- C11D7/00—Compositions of detergents based essentially on non-surface-active compounds
- C11D7/22—Organic compounds
- C11D7/26—Organic compounds containing oxygen
- C11D7/261—Alcohols; Phenols
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- 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
- C11D7/00—Compositions of detergents based essentially on non-surface-active compounds
- C11D7/22—Organic compounds
- C11D7/26—Organic compounds containing oxygen
- C11D7/263—Ethers
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- 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
- C11D7/00—Compositions of detergents based essentially on non-surface-active compounds
- C11D7/22—Organic compounds
- C11D7/26—Organic compounds containing oxygen
- C11D7/264—Aldehydes; Ketones; Acetals or ketals
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- 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
- C11D7/00—Compositions of detergents based essentially on non-surface-active compounds
- C11D7/22—Organic compounds
- C11D7/32—Organic compounds containing nitrogen
- C11D7/3227—Ethers thereof
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- 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
- C11D7/00—Compositions of detergents based essentially on non-surface-active compounds
- C11D7/50—Solvents
- C11D7/5004—Organic solvents
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- C11D2111/00—Cleaning compositions characterised by the objects to be cleaned; Cleaning compositions characterised by non-standard cleaning or washing processes
- C11D2111/10—Objects to be cleaned
- C11D2111/14—Hard surfaces
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- C11D—DETERGENT COMPOSITIONS; USE OF SINGLE SUBSTANCES AS DETERGENTS; SOAP OR SOAP-MAKING; RESIN SOAPS; RECOVERY OF GLYCEROL
- C11D2111/00—Cleaning compositions characterised by the objects to be cleaned; Cleaning compositions characterised by non-standard cleaning or washing processes
- C11D2111/10—Objects to be cleaned
- C11D2111/14—Hard surfaces
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Abstract
A method of removing cooked-, baked-, or burnt-on soil from cookware and tableware comprising delivering a plurality of compositions including at least one organic solvent composition into the same or different cycles of an automatic dishwashing machine and washing the soiled cookware/tableware in the resulting solvent-containing wash liquor. The method includes the storage and delivery of organic solvent compositions and dishwashing detergent composition from multi-compartment containers. The method provides excellent removal of stubborn soils which are very difficult to remove in a conventional automatic dishwashing process.
Description
AUTOMATIC DISHWASHING METHOD EMPLOYING
AN ORGANIC SOLVENT SYSTEM
Technical field The present invention is in the field of dishwashing, in particular it relates to dishwashing methods suitable for the removal of cooked-, baked- and burnt-on soils from cookware and tableware.
Background of the invention Cooked-, baked- and burnt-on soils are amongst the most severe types of soils to remove from surfaces. Traditionally, the removal of cooked-, baked- and burnt-on soils from cookware and tableware requires soaking the soiled object prior to a mechanical action.
Apparently, the automatic dishwashing process alone does not provide a satisfactory removal of cooked-, baked- and burnt-on soils. Manual dishwashing process requires a tremendous rubbing effort to remove cooked-, baked- and burnt-on soils and this can be detrimental to the safety and condition of the cookware/tableware.
The use of cleaning compositions containing solvent for helping in the removal of cooked-, baked- and burnt-on solids is known in the art. For example, US-A-5,102,573 provides a method for treating hard surfaces soiled with cooked-on, baked-on or dried-on food residues comprising applying a pre-spotting composition to the soiled article. The composition applied comprises surfactant, builder, amine and solvent. US-A-5,929,007 provides an aqueous hard surface cleaning composition for removing hardened dried or baked-on grease soil deposits. The composition comprises nonionic surfactant, chelating agent, caustic, a glycol ether solvent system, organic amine and anti-redeposition agents.
WO-A-94/28108 discloses an aqueous cleaner concentrate composition, that can be diluted to form a more viscous use solution comprising an effective thickening amount of a rod micelle thickener composition, lower alkyl glycol ether solvent and hardness sequestering agent. The application also describes a method of cleaning a food preparation unit having at least one substantially vertical surface having a baked food soil
AN ORGANIC SOLVENT SYSTEM
Technical field The present invention is in the field of dishwashing, in particular it relates to dishwashing methods suitable for the removal of cooked-, baked- and burnt-on soils from cookware and tableware.
Background of the invention Cooked-, baked- and burnt-on soils are amongst the most severe types of soils to remove from surfaces. Traditionally, the removal of cooked-, baked- and burnt-on soils from cookware and tableware requires soaking the soiled object prior to a mechanical action.
Apparently, the automatic dishwashing process alone does not provide a satisfactory removal of cooked-, baked- and burnt-on soils. Manual dishwashing process requires a tremendous rubbing effort to remove cooked-, baked- and burnt-on soils and this can be detrimental to the safety and condition of the cookware/tableware.
The use of cleaning compositions containing solvent for helping in the removal of cooked-, baked- and burnt-on solids is known in the art. For example, US-A-5,102,573 provides a method for treating hard surfaces soiled with cooked-on, baked-on or dried-on food residues comprising applying a pre-spotting composition to the soiled article. The composition applied comprises surfactant, builder, amine and solvent. US-A-5,929,007 provides an aqueous hard surface cleaning composition for removing hardened dried or baked-on grease soil deposits. The composition comprises nonionic surfactant, chelating agent, caustic, a glycol ether solvent system, organic amine and anti-redeposition agents.
WO-A-94/28108 discloses an aqueous cleaner concentrate composition, that can be diluted to form a more viscous use solution comprising an effective thickening amount of a rod micelle thickener composition, lower alkyl glycol ether solvent and hardness sequestering agent. The application also describes a method of cleaning a food preparation unit having at least one substantially vertical surface having a baked food soil
2 coating. In practice, however, none of the art has been found to be very effective in removing baked-on, polymerized soil from metal and other substrates.
The use of solvents in the automatic dishwashing context is also known. JP-A-10,017,900 discloses an automatic dishwashing auxiliary composition comprising non-ionic low foaming surfactant, organic solvent and water. The composition delivers detergency and drying benefits. JP-A-11,117,000 discloses a cleaning assistant composition for automatic dishwashing machines comprising surfactant, organic high-molecular polyelectrolyte, water-soluble solvent and water. The claimed assistant composition helps in the cleaning of stubborn dirt such as that due to oil or lipstick.
There is still the need for a method and products having improved efficacy for the removal of cooked-, baked- and burnt-on soils from cookware and tableware using an automatic dishwashing machine and avoiding the use of a pre-treatment step.
SununM of the invention According to a first aspect of the present invention, there is provided a method of removing cooked-, baked-, or burnt-on food soil (such as grease, meat, dairy, fruit, pasta and any other food especially difficult to remove after the cooking process) from cookware and tableware (including stainless steel, glass, plastic, wood and ceramic objects). The method comprises washing the cookware/tableware in an automatic dishwashing machine in presence of a plurality of compositions, including at least one organic solvent composition. The purpose of using a plurality of compositions is to have different compositions for the cleaning of the different soils and substrates present in a dishwashing machine load. The plurality of compositions are formulated not only for the basic cleaning purpose but also for providing the dishwashing load with good aesthetic features such as shine, filming, spotting, etc. Organic solvent compositions (comprising a single solvent compound or a mixture of solvent compounds) for use herein preferably have a volatile organic content above 1 mm Hg of less than about 50%, preferably less than about 20% and more preferably less than about 10% by weight of the solvent system.
The use of solvents in the automatic dishwashing context is also known. JP-A-10,017,900 discloses an automatic dishwashing auxiliary composition comprising non-ionic low foaming surfactant, organic solvent and water. The composition delivers detergency and drying benefits. JP-A-11,117,000 discloses a cleaning assistant composition for automatic dishwashing machines comprising surfactant, organic high-molecular polyelectrolyte, water-soluble solvent and water. The claimed assistant composition helps in the cleaning of stubborn dirt such as that due to oil or lipstick.
There is still the need for a method and products having improved efficacy for the removal of cooked-, baked- and burnt-on soils from cookware and tableware using an automatic dishwashing machine and avoiding the use of a pre-treatment step.
SununM of the invention According to a first aspect of the present invention, there is provided a method of removing cooked-, baked-, or burnt-on food soil (such as grease, meat, dairy, fruit, pasta and any other food especially difficult to remove after the cooking process) from cookware and tableware (including stainless steel, glass, plastic, wood and ceramic objects). The method comprises washing the cookware/tableware in an automatic dishwashing machine in presence of a plurality of compositions, including at least one organic solvent composition. The purpose of using a plurality of compositions is to have different compositions for the cleaning of the different soils and substrates present in a dishwashing machine load. The plurality of compositions are formulated not only for the basic cleaning purpose but also for providing the dishwashing load with good aesthetic features such as shine, filming, spotting, etc. Organic solvent compositions (comprising a single solvent compound or a mixture of solvent compounds) for use herein preferably have a volatile organic content above 1 mm Hg of less than about 50%, preferably less than about 20% and more preferably less than about 10% by weight of the solvent system.
3 Herein volatile organic content of the solvent system is defined as the content of organic components in the solvent system having a vapor pressure higher than the prescribed limit at 25 C and atmospheric pressure.
In preferred embodiments the plurality of compositions includes at least one organic solvent composition and at =least one automatic dishwashing detergent composition or the plurality of compositions includes two or more solvent compositions. The optimum concentration of solvent in the wash liquor is from about 100 ppm to about 10000 ppm, preferably from about 200 to about 8000 and more preferably from about 500 to about 5000 ppm. Preferably, the wash liquor has a liquid surface tension of less than about 35 mN/m, preferably less than about 32 mN/m more preferably less than about 30 mN/m and especially less than about 28 mN/m. The pH of the wash liquor will generally be in the alkaline range, preferably at least 10.5 or more preferably at least 11.0, this pH being provided by means of an alkalinity source or sources in one or more compositions used for delivery of the solvent, surfactant and builder.
The compositions of the invention can be delivered into the same or different cycles of the automatic dishwashing machine. The soiled cookware/tableware is washed in the resulting solvent-containing wash liquor.
Thus, according to another embodiment the removal of cooked-, baked-, or burnt-on food soil from cookware and tableware can be carried out by the use of a plurality of compositions, including one or more organic solvent compositions (wherein "solvent composition" is understood to comprise the organic solvent system and optional additional active ingredients and diluents) and one or more automatic dishwashing detergent compositions. The organic solvent composition can be built, unbuilt or generally unbuilt, but when used as an additive composition in conjunction with a dishwashing detergent composition, the solvent composition will normally be relatively unbuilt by comparison with the detergent composition. By "relatively unbuilt"
is meant that under normal use conditions, the solvent composition will deliver a minor proportion (less than 50%, preferably less than 25%, more preferably less than 10% by weight) of the
In preferred embodiments the plurality of compositions includes at least one organic solvent composition and at =least one automatic dishwashing detergent composition or the plurality of compositions includes two or more solvent compositions. The optimum concentration of solvent in the wash liquor is from about 100 ppm to about 10000 ppm, preferably from about 200 to about 8000 and more preferably from about 500 to about 5000 ppm. Preferably, the wash liquor has a liquid surface tension of less than about 35 mN/m, preferably less than about 32 mN/m more preferably less than about 30 mN/m and especially less than about 28 mN/m. The pH of the wash liquor will generally be in the alkaline range, preferably at least 10.5 or more preferably at least 11.0, this pH being provided by means of an alkalinity source or sources in one or more compositions used for delivery of the solvent, surfactant and builder.
The compositions of the invention can be delivered into the same or different cycles of the automatic dishwashing machine. The soiled cookware/tableware is washed in the resulting solvent-containing wash liquor.
Thus, according to another embodiment the removal of cooked-, baked-, or burnt-on food soil from cookware and tableware can be carried out by the use of a plurality of compositions, including one or more organic solvent compositions (wherein "solvent composition" is understood to comprise the organic solvent system and optional additional active ingredients and diluents) and one or more automatic dishwashing detergent compositions. The organic solvent composition can be built, unbuilt or generally unbuilt, but when used as an additive composition in conjunction with a dishwashing detergent composition, the solvent composition will normally be relatively unbuilt by comparison with the detergent composition. By "relatively unbuilt"
is meant that under normal use conditions, the solvent composition will deliver a minor proportion (less than 50%, preferably less than 25%, more preferably less than 10% by weight) of the
4 total builder delivered to the wash liquor by the one or more solvent compositions and the one or more detergent compositions. By "generally unbuilt" is meant that the composition contains less than about 5% by weight of detergency builder.
According to different embodiments of the present invention, the solvent compositions and automatic dishwashing detergent compositions can be delivered either at the same or at different points of the dishwashing cycle, for example: i) solvent composition and automatic dishwashing detergent composition are independently delivered in the pre-wash cycle and in the main-wash cycle, respectively; ii) a solvent composition and a first automatic dishwashing detergent composition are delivered in the pre-wash cycle and a second automatic dishwashing detergent composition in the main-wash cycle;
iii) a first solvent composition and a first automatic dishwashing detergent composition are delivered in the pre-wash cycle and a second solvent composition and a second automatic dishwashing detergent composition in the main-wash cycle; iv) a solvent composition and an automatic dishwashing detergent composition are delivered simultaneously in the main-wash cycle; and v) a solvent composition and an automatic dishwashing detergent composition are delivered in the pre-wash and in the main-wash cycle.
Another embodiment provides a method of removing cooked-, baked-, or burnt-on food soil from cookware and tableware comprising washing the cookware/tableware in the pre-wash cycle of an automatic 'dishwashing machine in the presence of an organic solvent composition and thereafter rinsing the cookware/tableware in the rinse cycle of the automatic dishwashing machine in the presence of an automatic dishwashing rinse composition.
In preferred embodiments, the organic solvent composition and the automatic dishwashing detergent composition are delivered either i) from separate storage means (e.g. different bottles in the case of liquid compositions, different pouches, etc.) into the same cycle of an automatic dishwashing machine. Preferably, the organic solvent composition provides a wash liquor concentration of organic solvent as prescribed herein and preferably in the range from about 100 to about 10000 ppm, preferably from about 500 to about 5000; or ii) from separate zones of a multi-zone storage means (e.g. multi-compartment bottle in the case of liquid compositions) into the same or different cycles of an automatic dishwashing machine. Suitably, the organic solvent composition and the automatic dishwashing detergent composition are delivered from separate zones of a multi-zone storage means at a feed ratio (solvent composition: detergent composition) in the range from about 5:1 to about 1:50, preferably from about 2:1 to about 1:6 and more preferably from about 1:1 to about 1:5 to provide a wash liquor concentration of organic solvent in the range preferably from about 100 to about 10000, more preferably from about 500 to about 5000 ppm. Alternatively, the organic solvent composition and the automatic dishwashing detergent composition are delivered from separate zones of a multi-zone storage means sequentially into the pre-wash and main wash cycle, respectively. This can be valuable in the case of product incompatibility to reduce interaction between the organic solvent composition and the automatic dishwashing detergent composition. Where, the organic solvent composition and the automatic dishwashing detergent composition are delivered simultaneously from separate zones of a multi-zone storage means, the physical form of the organic solvent composition and/or automatic dishwashing detergent composition is preferably such as to prevent intimate mixing of the compositions prior to contact thereof with the wash liquor.
The invention can be also reduced to practice using multi-phase, "all-in-one"
products.
Thus, according to another embodiment of the invention, there is provided a method of removing cooked-, baked-, or burnt-on food soil from cookware and tableware comprising delivering separate portions of a multi-phase detergent composition into the same or different cycles of an automatic dishwashing machine, wherein the multi-phase detergent composition comprises at least a first phase containing an organic solvent composition and at least a second phase containing an automatic dishwashing detergent composition. The multiphase detergent composition, for example could take the form of a multi-layer liquid (e.g. coacervate) or gel contained in a bottle, or a multiphase tablet incorporating the solvent composition in the form of a gel contained within a preformed cavity or recess within the main tablet body. In either instance, the level of solvent delivered to the wash process should be such as to deliver the benefits on cooked-, baked-or burnt-on food soils.
The present invention also envisages the use of multiple organic solvent compositions.
Thus according to another embodiment, there is provided a method of removing cooked-, baked-, or burnt-on food soil from cookware and tableware comprising delivering a plurality of organic solvent compositions of different solvent characteristics into the same or different cycles of an automatic dishwashing machine, for example, a first solvent composition in the pre-wash cycle and a second solvent composition in the main-wash cycle. For optimum performance, the different organic solvent compositions are designed to be specific to different soil and/or substrates. They can be delivered into different cycles of a dishwashing machine, with or without different automatic dishwashing detergent compositions, such that, for example, a first solvent composition and a first automatic dishwashing detergent composition are delivered into the pre-wash cycle and a second solvent composition and a second automatic dishwashing detergent composition are delivered into the main-wash cycle.
In another embodiment of the invention the organic solvent composition can be in a unit dose form allowing controlled release (for example delayed, sustained, triggered or slow release) of the composition during one or more repeated washing cycles.
Especially suitable are unit dose form allowing delayed release of organic solvent until after the pre-wash cycle. In preferred unit dose forms, the solvent composition is contained in a single or multi-compartment pouch.
In the methods of the invention the organic solvent composition can be in the form of a liquid, paste, cream or gel and can be optionally encapsulated, packaged in a single- or multi-compartment pouch, or absorbed onto a porous carrier material. The solvent composition can be aqueous but preferably is anhydrous. Preferred pouches for use herein are water-soluble, solvent-resistant partially hydrolysed PVA pouches.
Preferably organic solvent compositions for use herein comprise an organoamine solvent or other agent effective in removing the soil and have a liquid surface tension of less than about 24.5 mN/m, preferably less than about 24 mN/m, more preferably less than about 23.5 mN/m.
In preferred embodiments the organic solvent composition additionally comprises a spreading auxiliary. The function of the spreading auxiliary is to reduce the interfacial tension between the organic solvent and the soil, therefore increasing the wettability of soils by the organic solvents. The spreading auxiliary when added to the compositions herein containing organic solvents effective in removing the soil leads to a lowering in the surface tension of the compositions, preferred spreading auxiliaries being those which lower the surface tension below that of the auxiliary itself. Especially useful are spreading auxiliaries able to render a surface tension below about 30 mN/m, preferably below about 28 mN/m and more preferably below about 26 mN/m, and especially below about 24 mN/m. Surface tensions are measured herein at 25 C. Spreading auxiliaries for use herein can be selected from organic solvents, wetting agents and mixtures thereof.
The invention can also be applied to single-phase "all-in-one" products.
According to this aspect, a method of removing cooked-, baked-, or burnt-on food soil from cookware and tableware comprises washing the cookware/tableware in an automatic dishwashing machine with an automatic dishwashing detergent composition comprising surfactant (preferably comprising low-foaming nonionic surfactant), detergency builder and organic solvent system in levels sufficient to provide a wash liquor concentration of from about ppm to about 1000 ppm surfactant, from about 100 ppm to about 5000 ppm detergency builder, and about 100 ppm to about 10,000, preferably from about 500 ppm to about 5000 ppm of organic solvent.
The optimum organic solvent systems for use herein are characterised by extremely low liquid surface tensions and contact angles on polymerised grease-coated substrates.
Moreover, they generally consist of mixed solvent systems displaying synergistic contact angle and low surface tension. The organic solvent system herein preferably has a liquid surface tension at 25 C of less than about 27 mN/m, preferably less than 25 mN/m.
Suitable for the present invention are organic solvent systems comprising a plurality of solvent components in levels such that the solvent system has a surface tension less than, and preferably at least 1 mN/m less than that of any of the individual solvent components.
In terms of contact angle, compositions containing the solvent system preferably display an advancing contact angle on a polymerised grease-coated substrate at 25 C of less than 20 , preferably less than 10 and more preferably less than 5 . Furthermore, the advancing contact angle for compositions based on mixed solvent systems should be less than that of any of the corresponding compositions containing the individual components of the solvent system. Such solvent systems and compositions are found to be optimum for the removal of burnt-on soils having a high carbon content from cookware and tableware.
The method for determining contact angle is as follows. A sample plate (prepared as described below) is dipped into and pulled out of a liquid and contact angles calculated after Wilhelmy Method. The force exerted on the sample according to the immersion depth is measured (using a Kruss K12 tensiometer and System K121 software) and is proportional to the contact angle of the liquid on the solid surface. The sample plate is prepared as follows: Spray 30-50 grams of Canola Oil into a beaker. Dip a glass slide (3x9x0.1 cm) into the Oil and thoroughly coat the surface. This results in an evenly dispersed layer of oil on the surface. Adjust the weight of product on the slide's surface until approximately 0.5 g of oil has been delivered and _evenly distributed.
At this point, bake the slides at 450F for 20 minutes, and allow to cool to room temperature.
A broad range of organic solvents are suitable for use herein but preferably the organic solvent is selected from alcohols, amines, esters, glycol ethers, glycols, terpenes and mixtures thereof. The organic solvent system is preferably formulated to meet the constraints on volatile solvent components described above and in highly preferred embodiments the solvent system will contain less than about 50%, preferably less than 20% and more preferably less than 10% of solvent components having a vapor pressure above about 0.1 mm Hg at 25 C and atmospheric pressure. In highly preferred embodiments, the solvent is essentially free (contains less than about 5% by weight) of solvent components having a boiling point below about 150 C, flash point below about 100 C or a vapor pressure above about 1 mm Hg at 25 C and atmospheric pressure.
The organic solvent system for use herein is preferably selected from organoamine solvents, inclusive of alkanolamines, alkylamines, alkyleneamines and mixtures thereof;
alcoholic solvents inclusive of aromatic, aliphatic (preferably C4-Clo) and cycloaliphatic alcohols and mixtures thereof; glycols and glycol derivatives inclusive of C2-(poly)alkylene glycols, glycol ethers, glycol esters and mixtures thereof; and mixtures selected from organoamine solvents, alcoholic solvents, glycols and glycol derivatives. In one preferred embodiment the organic solvent comprises organoamine (especially alkanolamine, more especially 2-aminalkanol) solvent and glycol ether solvent, preferably in a weight ratio of from about 3:1 to about 1:3, and wherein the glycol ether solvent is selected from ethylene glycol monobutyl ether, diethylene glycol monobutyl ether, ethylene glycol monomethyl ether, ethylene glycol monoethyl ether, diethylene glycol monomethyl ether, diethylene glycol monoethyl ether, propylene glycol monobutyl ether, and mixtures thereof. Preferably, the glycol ether is a mixture of diethylene glycol monobutyl ether and propylene glycol butyl ether, especially in a weight ratio of from about 1:2 to about 2:1. ' In other preferred embodiments, suitable organic solvents include one or more water-soluble or dispersible, preferably hydroxylated organoamine solvents, especially alkanolamine solvents having a pKa of at least 8.8, preferably at least 9.3 and more preferably at least 9.8. In these embodiments, the organic solvent system preferably comprises a mixture of a first organoamine solvent having a pKa of about 9.5 or less and a second organoamine solvent having a pKa greater than about 9.5. Also preferred for use herein are organic solvents comprising salts of organoamines which are introduced into the wash liquor of the automatic dishwashing machine at a wash liquor pH above the highest pKa of the organoamine and which thereby act as a source of organoanmine solvent. Suitable salt counterions include halides such as chloride and bromide, oxyanions such as sulphate, borate, phosphate, pyrophosphate and polyphosphate and surfactant anions.
In a preferred embodiment the organic solvent comprises one" or more organoamines which is/are introduced into the wash liquor of an automatic dishwashing machine in the form of their ammonium salt at a wash liquor pH above the highest pKa of the organoamine/s.
The effect of the solvent system can be further improved by the addition of certain wetting agents. Preferably, the organic solvent system is used in conjunction with a wetting agent effective in lowering the surface tension of the solvent system, preferably to at least 1 mN/m less than that of the wetting agent, the wetting agent preferably being selected from organic surfactants having a surface tension less than about 30 mN/m, more preferably less than about 28 mN/m and specially less than about 26 mN/m. Preferred wetting agents for use herein are silicone polyether copolymers, especially silicone poly(alkyleneoxide) copolymers wherein alkylene is selected from ethylene, propylene and mixtures thereof.
In terms of solvent parameters, the organic solvent can be selected from:
a) polar, hydrogen-bonding solvents having a Hansen solubility parameter of at least 20 (Mpa)"2, a polarity parameter of at least 7(Mpa)1/2, preferably at least 12 (Mpa) 1/2 and a hydrogen bonding parameter of at least 10 (Mpa)1i2 b) polar non-hydrogen bonding solvents.having a Hansen solubility parameter of at least (Mpa)1/z, a polarity parameter of at least 7(Mpa)1/2, preferably at least 12 (Mpa)1i2 and a hydrogen bonding parameter of less than 10 (Mpa)1i2 c) amphiphilic solvents having a Hansen solubility parameter below 20 (Mpa)1/2, a polarity parameter of at least 7(Mpa)1/2 and a hydrogen bonding parameter of at least 10 (Mpa)ii2 d) non-polar solvents having a polarity parameter below 7(Mpa)1/2 and a hydrogen bonding parameter below 10 (Mpa)1/2 and e) mixtures thereof.
The invention also relates to detergent packs and multi-component products suitable for use in an automatic dishwashing machine or dishwashing pretreatment to provide baked and burnt-on soil removal and other cleaning benefits. In one embodiment, there is provided an automatic dishwashing detergent pack comprising two or more automatic dishwashing detergent and/or auxiliary products, storage means comprising separate but associated portions<of the two or more products and means, for example electric pump means, for delivering quantities of the two or more products into the same or different cycles of an automatic dishwashing machine. The pack can also comprise means for controlling the relative dispensing rate of the two or more products from the storage means. The pack preferably comprises an organic solvent composition and an automatic dishwashing detergent composition and is used for removing cooked-, baked-, and burnt-on food soil from cookware and tableware. In a preferred embodiment the two or more automatic dishwashing detergent or auxiliary products are in rheology-matched gel-form.
Compositions are considered to be rheology-matched if they have similar yield values (differing by less than about 50%, preferably by less than about 20%) and/or similar viscosities (differing by less than about 50%, preferably by less than about 20%) under the same shear conditions.
The invention also relates to organic solvent compositions suitable for use in automatic dishwashing. In one embodiment, an organic solvent composition comprises about 1% to about 99%, preferably from about 5% to about 90% of an organic solvent system for reinoving cooked-, baked-, or burnt-on food soil from cookware and tableware, from about 0.5% to about 50%, preferably from about 5% to about 25% of bleach and from about 0.0001% to about 10% of detergency enzyme. The compositions preferably are in gel-form and contain a thickener such as methylcellulose or other nonionic cellulosic thickener. The solvent compositions are preferably anhydrous (containing less than about
According to different embodiments of the present invention, the solvent compositions and automatic dishwashing detergent compositions can be delivered either at the same or at different points of the dishwashing cycle, for example: i) solvent composition and automatic dishwashing detergent composition are independently delivered in the pre-wash cycle and in the main-wash cycle, respectively; ii) a solvent composition and a first automatic dishwashing detergent composition are delivered in the pre-wash cycle and a second automatic dishwashing detergent composition in the main-wash cycle;
iii) a first solvent composition and a first automatic dishwashing detergent composition are delivered in the pre-wash cycle and a second solvent composition and a second automatic dishwashing detergent composition in the main-wash cycle; iv) a solvent composition and an automatic dishwashing detergent composition are delivered simultaneously in the main-wash cycle; and v) a solvent composition and an automatic dishwashing detergent composition are delivered in the pre-wash and in the main-wash cycle.
Another embodiment provides a method of removing cooked-, baked-, or burnt-on food soil from cookware and tableware comprising washing the cookware/tableware in the pre-wash cycle of an automatic 'dishwashing machine in the presence of an organic solvent composition and thereafter rinsing the cookware/tableware in the rinse cycle of the automatic dishwashing machine in the presence of an automatic dishwashing rinse composition.
In preferred embodiments, the organic solvent composition and the automatic dishwashing detergent composition are delivered either i) from separate storage means (e.g. different bottles in the case of liquid compositions, different pouches, etc.) into the same cycle of an automatic dishwashing machine. Preferably, the organic solvent composition provides a wash liquor concentration of organic solvent as prescribed herein and preferably in the range from about 100 to about 10000 ppm, preferably from about 500 to about 5000; or ii) from separate zones of a multi-zone storage means (e.g. multi-compartment bottle in the case of liquid compositions) into the same or different cycles of an automatic dishwashing machine. Suitably, the organic solvent composition and the automatic dishwashing detergent composition are delivered from separate zones of a multi-zone storage means at a feed ratio (solvent composition: detergent composition) in the range from about 5:1 to about 1:50, preferably from about 2:1 to about 1:6 and more preferably from about 1:1 to about 1:5 to provide a wash liquor concentration of organic solvent in the range preferably from about 100 to about 10000, more preferably from about 500 to about 5000 ppm. Alternatively, the organic solvent composition and the automatic dishwashing detergent composition are delivered from separate zones of a multi-zone storage means sequentially into the pre-wash and main wash cycle, respectively. This can be valuable in the case of product incompatibility to reduce interaction between the organic solvent composition and the automatic dishwashing detergent composition. Where, the organic solvent composition and the automatic dishwashing detergent composition are delivered simultaneously from separate zones of a multi-zone storage means, the physical form of the organic solvent composition and/or automatic dishwashing detergent composition is preferably such as to prevent intimate mixing of the compositions prior to contact thereof with the wash liquor.
The invention can be also reduced to practice using multi-phase, "all-in-one"
products.
Thus, according to another embodiment of the invention, there is provided a method of removing cooked-, baked-, or burnt-on food soil from cookware and tableware comprising delivering separate portions of a multi-phase detergent composition into the same or different cycles of an automatic dishwashing machine, wherein the multi-phase detergent composition comprises at least a first phase containing an organic solvent composition and at least a second phase containing an automatic dishwashing detergent composition. The multiphase detergent composition, for example could take the form of a multi-layer liquid (e.g. coacervate) or gel contained in a bottle, or a multiphase tablet incorporating the solvent composition in the form of a gel contained within a preformed cavity or recess within the main tablet body. In either instance, the level of solvent delivered to the wash process should be such as to deliver the benefits on cooked-, baked-or burnt-on food soils.
The present invention also envisages the use of multiple organic solvent compositions.
Thus according to another embodiment, there is provided a method of removing cooked-, baked-, or burnt-on food soil from cookware and tableware comprising delivering a plurality of organic solvent compositions of different solvent characteristics into the same or different cycles of an automatic dishwashing machine, for example, a first solvent composition in the pre-wash cycle and a second solvent composition in the main-wash cycle. For optimum performance, the different organic solvent compositions are designed to be specific to different soil and/or substrates. They can be delivered into different cycles of a dishwashing machine, with or without different automatic dishwashing detergent compositions, such that, for example, a first solvent composition and a first automatic dishwashing detergent composition are delivered into the pre-wash cycle and a second solvent composition and a second automatic dishwashing detergent composition are delivered into the main-wash cycle.
In another embodiment of the invention the organic solvent composition can be in a unit dose form allowing controlled release (for example delayed, sustained, triggered or slow release) of the composition during one or more repeated washing cycles.
Especially suitable are unit dose form allowing delayed release of organic solvent until after the pre-wash cycle. In preferred unit dose forms, the solvent composition is contained in a single or multi-compartment pouch.
In the methods of the invention the organic solvent composition can be in the form of a liquid, paste, cream or gel and can be optionally encapsulated, packaged in a single- or multi-compartment pouch, or absorbed onto a porous carrier material. The solvent composition can be aqueous but preferably is anhydrous. Preferred pouches for use herein are water-soluble, solvent-resistant partially hydrolysed PVA pouches.
Preferably organic solvent compositions for use herein comprise an organoamine solvent or other agent effective in removing the soil and have a liquid surface tension of less than about 24.5 mN/m, preferably less than about 24 mN/m, more preferably less than about 23.5 mN/m.
In preferred embodiments the organic solvent composition additionally comprises a spreading auxiliary. The function of the spreading auxiliary is to reduce the interfacial tension between the organic solvent and the soil, therefore increasing the wettability of soils by the organic solvents. The spreading auxiliary when added to the compositions herein containing organic solvents effective in removing the soil leads to a lowering in the surface tension of the compositions, preferred spreading auxiliaries being those which lower the surface tension below that of the auxiliary itself. Especially useful are spreading auxiliaries able to render a surface tension below about 30 mN/m, preferably below about 28 mN/m and more preferably below about 26 mN/m, and especially below about 24 mN/m. Surface tensions are measured herein at 25 C. Spreading auxiliaries for use herein can be selected from organic solvents, wetting agents and mixtures thereof.
The invention can also be applied to single-phase "all-in-one" products.
According to this aspect, a method of removing cooked-, baked-, or burnt-on food soil from cookware and tableware comprises washing the cookware/tableware in an automatic dishwashing machine with an automatic dishwashing detergent composition comprising surfactant (preferably comprising low-foaming nonionic surfactant), detergency builder and organic solvent system in levels sufficient to provide a wash liquor concentration of from about ppm to about 1000 ppm surfactant, from about 100 ppm to about 5000 ppm detergency builder, and about 100 ppm to about 10,000, preferably from about 500 ppm to about 5000 ppm of organic solvent.
The optimum organic solvent systems for use herein are characterised by extremely low liquid surface tensions and contact angles on polymerised grease-coated substrates.
Moreover, they generally consist of mixed solvent systems displaying synergistic contact angle and low surface tension. The organic solvent system herein preferably has a liquid surface tension at 25 C of less than about 27 mN/m, preferably less than 25 mN/m.
Suitable for the present invention are organic solvent systems comprising a plurality of solvent components in levels such that the solvent system has a surface tension less than, and preferably at least 1 mN/m less than that of any of the individual solvent components.
In terms of contact angle, compositions containing the solvent system preferably display an advancing contact angle on a polymerised grease-coated substrate at 25 C of less than 20 , preferably less than 10 and more preferably less than 5 . Furthermore, the advancing contact angle for compositions based on mixed solvent systems should be less than that of any of the corresponding compositions containing the individual components of the solvent system. Such solvent systems and compositions are found to be optimum for the removal of burnt-on soils having a high carbon content from cookware and tableware.
The method for determining contact angle is as follows. A sample plate (prepared as described below) is dipped into and pulled out of a liquid and contact angles calculated after Wilhelmy Method. The force exerted on the sample according to the immersion depth is measured (using a Kruss K12 tensiometer and System K121 software) and is proportional to the contact angle of the liquid on the solid surface. The sample plate is prepared as follows: Spray 30-50 grams of Canola Oil into a beaker. Dip a glass slide (3x9x0.1 cm) into the Oil and thoroughly coat the surface. This results in an evenly dispersed layer of oil on the surface. Adjust the weight of product on the slide's surface until approximately 0.5 g of oil has been delivered and _evenly distributed.
At this point, bake the slides at 450F for 20 minutes, and allow to cool to room temperature.
A broad range of organic solvents are suitable for use herein but preferably the organic solvent is selected from alcohols, amines, esters, glycol ethers, glycols, terpenes and mixtures thereof. The organic solvent system is preferably formulated to meet the constraints on volatile solvent components described above and in highly preferred embodiments the solvent system will contain less than about 50%, preferably less than 20% and more preferably less than 10% of solvent components having a vapor pressure above about 0.1 mm Hg at 25 C and atmospheric pressure. In highly preferred embodiments, the solvent is essentially free (contains less than about 5% by weight) of solvent components having a boiling point below about 150 C, flash point below about 100 C or a vapor pressure above about 1 mm Hg at 25 C and atmospheric pressure.
The organic solvent system for use herein is preferably selected from organoamine solvents, inclusive of alkanolamines, alkylamines, alkyleneamines and mixtures thereof;
alcoholic solvents inclusive of aromatic, aliphatic (preferably C4-Clo) and cycloaliphatic alcohols and mixtures thereof; glycols and glycol derivatives inclusive of C2-(poly)alkylene glycols, glycol ethers, glycol esters and mixtures thereof; and mixtures selected from organoamine solvents, alcoholic solvents, glycols and glycol derivatives. In one preferred embodiment the organic solvent comprises organoamine (especially alkanolamine, more especially 2-aminalkanol) solvent and glycol ether solvent, preferably in a weight ratio of from about 3:1 to about 1:3, and wherein the glycol ether solvent is selected from ethylene glycol monobutyl ether, diethylene glycol monobutyl ether, ethylene glycol monomethyl ether, ethylene glycol monoethyl ether, diethylene glycol monomethyl ether, diethylene glycol monoethyl ether, propylene glycol monobutyl ether, and mixtures thereof. Preferably, the glycol ether is a mixture of diethylene glycol monobutyl ether and propylene glycol butyl ether, especially in a weight ratio of from about 1:2 to about 2:1. ' In other preferred embodiments, suitable organic solvents include one or more water-soluble or dispersible, preferably hydroxylated organoamine solvents, especially alkanolamine solvents having a pKa of at least 8.8, preferably at least 9.3 and more preferably at least 9.8. In these embodiments, the organic solvent system preferably comprises a mixture of a first organoamine solvent having a pKa of about 9.5 or less and a second organoamine solvent having a pKa greater than about 9.5. Also preferred for use herein are organic solvents comprising salts of organoamines which are introduced into the wash liquor of the automatic dishwashing machine at a wash liquor pH above the highest pKa of the organoamine and which thereby act as a source of organoanmine solvent. Suitable salt counterions include halides such as chloride and bromide, oxyanions such as sulphate, borate, phosphate, pyrophosphate and polyphosphate and surfactant anions.
In a preferred embodiment the organic solvent comprises one" or more organoamines which is/are introduced into the wash liquor of an automatic dishwashing machine in the form of their ammonium salt at a wash liquor pH above the highest pKa of the organoamine/s.
The effect of the solvent system can be further improved by the addition of certain wetting agents. Preferably, the organic solvent system is used in conjunction with a wetting agent effective in lowering the surface tension of the solvent system, preferably to at least 1 mN/m less than that of the wetting agent, the wetting agent preferably being selected from organic surfactants having a surface tension less than about 30 mN/m, more preferably less than about 28 mN/m and specially less than about 26 mN/m. Preferred wetting agents for use herein are silicone polyether copolymers, especially silicone poly(alkyleneoxide) copolymers wherein alkylene is selected from ethylene, propylene and mixtures thereof.
In terms of solvent parameters, the organic solvent can be selected from:
a) polar, hydrogen-bonding solvents having a Hansen solubility parameter of at least 20 (Mpa)"2, a polarity parameter of at least 7(Mpa)1/2, preferably at least 12 (Mpa) 1/2 and a hydrogen bonding parameter of at least 10 (Mpa)1i2 b) polar non-hydrogen bonding solvents.having a Hansen solubility parameter of at least (Mpa)1/z, a polarity parameter of at least 7(Mpa)1/2, preferably at least 12 (Mpa)1i2 and a hydrogen bonding parameter of less than 10 (Mpa)1i2 c) amphiphilic solvents having a Hansen solubility parameter below 20 (Mpa)1/2, a polarity parameter of at least 7(Mpa)1/2 and a hydrogen bonding parameter of at least 10 (Mpa)ii2 d) non-polar solvents having a polarity parameter below 7(Mpa)1/2 and a hydrogen bonding parameter below 10 (Mpa)1/2 and e) mixtures thereof.
The invention also relates to detergent packs and multi-component products suitable for use in an automatic dishwashing machine or dishwashing pretreatment to provide baked and burnt-on soil removal and other cleaning benefits. In one embodiment, there is provided an automatic dishwashing detergent pack comprising two or more automatic dishwashing detergent and/or auxiliary products, storage means comprising separate but associated portions<of the two or more products and means, for example electric pump means, for delivering quantities of the two or more products into the same or different cycles of an automatic dishwashing machine. The pack can also comprise means for controlling the relative dispensing rate of the two or more products from the storage means. The pack preferably comprises an organic solvent composition and an automatic dishwashing detergent composition and is used for removing cooked-, baked-, and burnt-on food soil from cookware and tableware. In a preferred embodiment the two or more automatic dishwashing detergent or auxiliary products are in rheology-matched gel-form.
Compositions are considered to be rheology-matched if they have similar yield values (differing by less than about 50%, preferably by less than about 20%) and/or similar viscosities (differing by less than about 50%, preferably by less than about 20%) under the same shear conditions.
The invention also relates to organic solvent compositions suitable for use in automatic dishwashing. In one embodiment, an organic solvent composition comprises about 1% to about 99%, preferably from about 5% to about 90% of an organic solvent system for reinoving cooked-, baked-, or burnt-on food soil from cookware and tableware, from about 0.5% to about 50%, preferably from about 5% to about 25% of bleach and from about 0.0001% to about 10% of detergency enzyme. The compositions preferably are in gel-form and contain a thickener such as methylcellulose or other nonionic cellulosic thickener. The solvent compositions are preferably anhydrous (containing less than about
5%, preferably less than about 1% of water) and comprise bleach in the form of a particulate suspension having an average particle size in the range from about 10 to about 100 m, preferably from about 25 to about 75 m. The compositions are also builder free or generally builder free. It is a feature of the invention that a broad range of solvents,
6 PCT/US00/34909 including organoamine solvents can be incorporated in the solvent compositions of the invention with acceptable bleach stability provided the water content of the composition is carefully controlled.
The invention also relates to detergent compositions suitable for use in automatic dishwashing or dishwashing pretreatment. In one embodiment, an automatic dishwashing detergent composition comprises from about 0.05% to about 10% by weight of a low-foaming non-ionic surfactant, from about 1% to about 30% of an organoamine, preferably alkanolarnine (especially monoethanolamine) solvent and at least about 5% by weight of a detergency builder. Preferably, the automatic dishwashing detergent composition is in the form of a gel comprising from about 2% to about 20%, preferably from 5% to 15%
by weight of an alkanolamine, at least about 5% by weight of detergency builder, and from about 0.1% to about 5% by weight of a low foaming non-ionic surfactant.
Although any non-ionic low foaming surfactant (or combination of non-ionic surfactants and suds suppressers) can be used herein, capped nonionic surfactants and combinations or amine oxide and capped non-ionic surfactants are preferred. The compositions also preferably have a pH (1% aqueous solution) in excess of about 9.0, preferably in excess of about 10.5 and more preferably greater than about 11.
In one embodiment, an automatic dishwashing detergent composition comprises from about 0.05% to about 10% by weight of a low-foaming non-ionic surfactant, from about 1% to about 30% of an organic solvent, preferably alkanolamine solvent, at least about 5% by weight of a detergency builder and a wetting agent, preferably a silicone-poly(alkyleneoxide) copolymers.
In a preferred embodiment an automatic dishwashing detergent pack is provided, comprising: i) an organic solvent composition suitable for use in automatic dishwashing comprising from about 1% to about 99%, preferably from about 5% to about 90%, especially from about 40% to about 80% of an organic solvent system for removing cooked-, baked-, or burnt-on food soil from cookware and tableware, from about 0.5% to about 50%, preferably from about 5% to about 25% of bleach, from about 0.0001%
to about 10% of detergency enzyme, and wherein the composition is in the form of an anhydrous gel comprising bleach in the form of a particulate suspension; and ii) an automatic dishwashing detergent composition comprising from about 0.05% to about 10% by weight of a low-foaming non-ionic surfactant, optionally from about 1%
to about 30% of an organoamine, preferably alkanolamine solvent, and at least about 5%
by weight of a detergency builder. Preferably, the automatic dishwashing detergent composition is in the form of a gel comprising from about 2% to about 20%, preferably from about 5% to about 15% by weight of the composition of an alkanolamine, at least about 5%
by weight of detergency builder (such as sodium potassium tripolyphosphate), and from about 0.1%
to about 5% by weight of the composition of a low foaming non-ionic surfactant.
The compositions of the invention are also characterised by having a low volatile organic content, preferably with a volatile organic content less than about 20%, preferably less than about 10% and more preferably less than about 5%.
Suitable thickening agents for use in the solvent compositions and dishwashing detergent compositions herein include viscoelastic, thixotropic thickening agents at levels of from about 0.1% to about 10%, preferably from about 0.25% to about 5%, most preferably from about 0.5% to about 3% by weight. Suitable thickening agents include polymers with a molecular weight from about 500,000 to about 10,000,000, more preferably from about 750,000 to about 4,000,000. The preferred cross-linked polycarboxylate polymer is preferably a carboxyvinyl polymer. Such compounds are disclosed in U.S. Pat.
No.
2,798,053, issued on Jul. 2, 1957, to Brown. Methods for making carboxyvinyl polymers are also disclosed in Brown. Carboxyvinyl polymers are substantially insoluble in liquid, volatile organic hydrocarbons and are dimensionally stable on exposure to air.
Preferred polyhydric alcohols used to produce carboxyvinyl polymers include polyols selected from the class consisting of oligosaccarides, reduced derivatives thereof in which the carbonyl group is converted to an alcohol group, an pentaerythritol; most preferred is sucrose or pentaerythritol. It is preferred that the hydroxyl groups of the modified polyol be etherified with alkyl groups, the polyol having at least two allyl ether groups per polyol molecule. When the polyol is sucrose, it is preferred that the sucrose have at least about five allyl ether groups per sucrose molecule. It is preferred that the polyether of the polyol comprise from about 0.1% to about 4% of the total monomers, more preferably from about 0.2% to about 2.5%.
Preferred monomeric olefinically unsaturated carboxylic acids for use in producing carboxyvinyl polymers used herein include monomeric, polymerizable, alpha-beta monoolefinically unsaturated lower aliphatic carboxylic acids; more preferred are monomeric monoolefinic acrylic acids of the structure:
CHCH2=C(R)-COOH
where R is a substituent selected from the group consisting of hydrogen and lower alkyl groups; most preferred is acrylic acid.
Various carboxyvinyl polymers, homopolymers and copolymers are commercially available from B. F. Goodrich Company, New York, N.Y., under the trade name Carbopol0. These polymers are also known as carbomers or polyacrylic acids.
Carboxyvinyl polymers useful in formulations of the present invention include Carbopol 910 having a molecular weight of about 750,000, Carbopol 941 having a molecular weight of about 1,250,000, and Carbopols 934 and 940 having molecular weights of about 3,000,000 and 4,000,000, respectively. More preferred are the series of Carbopols which use ethyl acetate and cyclohexane in the manufacturing process, Carbopol 981, 2984, 980, and 1382.
Preferred polycarboxylate polymers are non-linear, water-dispersible, polyacrylic acid cross-linked with a polyalkenyl polyether and having a molecular weight of from about 750,000 to about 4,000,000.
Highly preferred examples of these polycarboxylate polymers for use in the present invention are Sokalan PHC-25 , a polyacrylic acid available from BASF
Corporation, the Carbopol 600 series resins available from B. F. Goodrich, and more preferred is Polygel DK available from 3-V Chemical Corporation. Mixtures of polycarboxylate polymers as herein described may also be used in the present invention.
Other suitable thickening agents include inorganic clays (e.g. laponites, aluminium silicate, bentonite, fumed silica). The preferred clay thickening agent can be either naturalIy occurring or synthetic. Preferred synthetic clays include the synthetic smectite-type clay sold under the trademark Laponite by Southern Clay Products, Inc.
Particularly useful are gel forming grades such as Laponite RD and sol forming grades such as Laponite RDS. Natural occumng clays include some smectite and attapulgite clays.
Mixtures of clays and polymeric thickeners are also suitable for use herein.
Other types of thickeners which can be used in this composition include natural gums, such as xanthan gum, locust bean gum, guar gum, and the like. The cellulosic type thickeners: hydroxyethyl and hydroxymethyl cellulose (ETHOCEL and METHOCEL
available from Dow Chemical) can also be used.
It is a feature of the invention that many of the solvent systems and compositions of the invention that are optimum for cleaning also demonstrate improved compatibility with partially hydrolysed PVA pouch materials of known construction and type. This is particularly surprising given that many well-known polar/or hydrolysed bonding solvent materials (for example the ethanolamines) in themselves have low compatibility with PVA materials and present serious issues for product stability. Solvent systems comprising mixtures of polar hydrogen bonding solvents (such as the organoamines) with a cosolvent selected from polar non-hydrogen bonding, amphiphilic and non-polar solvents and mixtures thereof are particularly valuable in this respect. Also valuable for improved PVA compatibility are organoamines present in composition in the form of amine salt. Also valuable for improved PVA compatibility are solvent systems and components based on propanolamines such as 2-amino-2-methyl propanol.
Compositions suitable for inclusion in pouches will normally comprise a major proportion of solvent system components, preferably at least 50% by weight, more preferably at least 70% by weight or even higher.
Detailed description of the invention The present invention envisages the use of plurality of compositions including at least one organic solvent composition into the same or different cycles of an automatic dishwashing machine and washing the soiled cookware/tableware in the resulting solvent-containing wash liquor. It also envisages multi-component dishwashing products containing purpose-designated combination of solvent compositions and dishwashing detergent compositions. The invention also envisages so called "all-in-one" detergent products having both an alkaline detergent and a solvent functionality. In the case of additive and multi-component products, the invention does not require the two compositions to be in the same physical form. The organic solvent composition can be in any physical form, e.g. liquid, paste, cream, gel, powder, granules or tablets and similarly the automatic dishwashing detergent composition can be in any of these forms. Preferably, however, both compositions are in the form of liquids or gels or the organic solvent composition is in the form of liquid or gel and the automatic dishwashing detergent composition is in the form of powder, granules or tablet. The compositions used herein can be dispensed from any suitable device, such as bottles (pump assisted bottles, squeeze bottles), paste dispensers, capsules, multi-compartment bottles, multi-compartment capsules, pouches, and multi-compartment pouches, etc.
The solvent compositions herein comprise one or more organic solvents and can additionally comprises surfactant, bleach, enzyme, enzyme stabilising components, thickener, etc.
The organic solvents should be selected so as to be compatible with the tableware/cookware as well as with the different parts of an automatic dishwashing machine. Furthermore, the solvent system should be effective and safe to use having a volatile organic content above 1 mm Hg (and preferably above 0.1 mm Hg) of less than about 50%, preferably less than about 30%, more preferably less than about 10%
by weight of the solvent system. Also they should have very mild pleasant odours.
The individual organic solvents used herein generally have a boiling point above about 150 C,.
flash point above about 100 C and vapor pressure below about 1 mm Hg, preferably below 0.1 mm Hg at 25 C and atmospheric pressure.
Solvents that can be used herein include: i) alcohols, such as benzyl alcohol, 1,4-cyclohexanedimethanol, 2-ethyl-l-hexanol, furfuryl alcohol, 1,2-hexanediol and other similar materials; ii) amines, such as alkanolamines (e.g. primary alkanolamines:
monoethanolamine, monoisopropanolamine, diethylethanolamine, ethyl diethanolamine, beta-aminoalkanols; secondary alkanolamines: diethanolamine, diisopropanolamine, 2-(methylamino)ethanol; ternary alkanolamines: triethanolamine, triisopropanolamine);
alkylamines (e.g. primary alkylamines: monomethylamine, monoethylamine, monopropylamine, monobutylamine, monopentylamine, cyclohexylamine), secondary alkylamines: (dimethylamine), alkylene amines (primary alkylene amines:
ethylenediamine, propylenediamine) and other similar materials; iii) esters, such as ethyl lactate, methyl ester, ethyl acetoacetate, ethylene glycol monobutyl ether acetate, diethylene glycol monoethyl ether acetate, diethylene glycol monobutyl ether acetate and other similar materials; iv) glycol ethers, such as ethylene glycol monobutyl ether, diethylene glycol monobutyl ether, ethylene glycol monomethyl ether, ethylene glycol monoethyl ether, diethylene glycol monomethyl ether, diethylene glycol monoethyl ether, propylene glycol butyl ether and other similar materials; v) glycols, such as propylene glycol, diethylene glycol, hexylene glycol (2-methyl-2, 4 pentanediol), triethylene glycol, composition and dipropylene glycol and other similar materials; and mixtures thereof.
Preferred solvents effective in removing cooked-, baked- or burnt-on food soil to be used herein coinprise alkanolamines, especially monoethanolamine, beta-aminoalkanols, especially 2-amino-2-methyl-propanol (since it has the lowest molecular weight of any beta-aminoalkanol which has the amine group attached to a tertiary carbon, therefore minimize the reactivity of the amine group) and mixtures thereof.
The detergent and cleaning compositions herein can comprise traditional detergency components and can also comprise organic solvents having a cleaning function and organic solvents having a carrier or diluent function or some other specialised function.
The cornpositions will generally be built and comprise one or more detergent active components which may be selected from colorants, bleaching agents, surfactants, alkalinity sources, enzymes, thickeners (in the case of liquid, paste, cream or gel compositions), anti-corrosion agents (e.g. sodium silicate), hydrotropes (e.g.
sodium cumene sulfate) and disrupting and binding agents (in the case of powder, granules or tablets). Highly preferred detergent components include a builder compound, an alkalinity source, a surfactant, an enzyme and a bleaching agent.
Unless otherwise specified, the components described hereinbelow can be incorporated either in the organic solvent compositions and/or the detergent or cleaning compositions.
Surfactant In the methods of the present invention for use in automatic dishwashing the detergent surfactant is preferably low foaming by itself or in combination with other components (i.e. suds suppressers). In compositions and methods of the present invention for use in hard surface cleaning or pretreatment prior to dishwashing, the detergent surfactant is preferably foamable in direct application but low foaming in automatic dishwashing use.
Surfactants suitable herein include anionic surfactants such as alkyl sulfates, alkyl ether sulfates, alkyl benzene sulfonates, alkyl glyceryl sulfonates, alkyl and alkenyl sulphonates, alkyl ethoxy carboxylates, N-acyl sarcosinates, N-acyl taurates and alkyl succinates and sulfosuccinates, wherein the alkyl, alkenyl or acyl moiety is C5-C20 , preferably C10-C18 linear or branched; cationic surfactants such as chlorine esters (US-A-4228042, US-A-4239660 and US-A-4260529) and mono C6-C16 N-alkyl or alkenyl ammonium surfactants wherein the remaining N positions are substituted by methyl, hydroxyethyl or hydroxypropyl groups; low and high cloud point nonionic surfactants and mixtures thereof including nonionic alkoxylated surfactants (especially ethoxylates derived from C6-C18 primary alcohols), ethoxylated-propoxylated alcohols (e.g., Olin Corporation's Poly-Tergent SLF18), epoxy-capped poly(oxyalkylated) alcohols (e.g., Olin Corporation's Poly-Tergent SLF18B - see WO-A-94/22800), ether-capped poly(oxyalkylated) alcohol surfactants, and block polyoxyethylene-polyoxypropylene polymeric compounds such as PLURONICO, REVERSED PLURONICO, and TETRONICO by the BASF-Wyandotte Corp., Wyandotte, Michigan; amphoteric surfactants such as the C12-C20 alkyl amine oxides (preferred ainine oxides for use herein include lauryldimethyl amine oxide and hexadecyl dimethyl amine oxide), and alkyl amphocarboxylic surfactants such as MiranolTM C2M; and zwitterionic surfactants such as the betaines and sultaines; and mixtures thereof. Surfactants suitable herein are disclosed, for example, in US-A-3,929,678 , US-A- 4,259,217, EP-A-0414 549, WO-A-93/08876 and WO-A-93/08874. Surfactants are typically present at a level of from about 0.2% to about 30% by weight, more preferably from about 0.5% to about 10% by weight, most preferably from about 1% to about 5% by weight of composition. Preferred surfactant for use herein are low foaming and include low cloud point nonionic surfactants and mixtures of higher foaming surfactants with low cloud point nonionic surfactants which act as suds suppresser therefor.
Builder Builders suitable for use herein include water-soluble builders such as citrates, carbonates and polyphosphates e.g. sodium tripolyphosphate and sodium tripolyphosphate hexahydrate, potassium tripolyphosphate and mixed sodium and potassium tripolyphosphate salts; and partially water-soluble or insoluble builders such as crystalline layered silicates (EP-A-0164514 and EP-A-0293640) and aluminosilicates inclusive of Zeolites A, B, P, X, HS and MAP. The builder is typically present at a level of from about 1% to about 80% by weight, preferably from about 10% to about 70% by weight, most preferably from about 20% to about 60% by weight of composition.
Amorphous sodium silicates having an Si02:Na20 ratio of from 1.8 to 3.0, preferably from 1.8 to 2.4, most preferably 2.0 can also be used herein although highly preferred from the viewpoint of long term storage stability are compositions containing less than about 22%, preferably less than about 15% total (amorphous and crystalline) silicate.
Enzyme Enzymes suitable herein include bacterial and fungal cellulases such as Carezyme and Celluzyme (Novo Nordisk A/S); peroxidases; lipases such as Amano-P (Amano Pharmaceutical Co.), Ml LipaseR and LipomaxR (Gist-Brocades) and LipolaseR and Lipolase UltraR (Novo); cutinases; proteases such as EsperaseR, AlcalaseR, DurazymR and SavinaseR (Novo) and MaxataseR, Maxacali ; ProperaseR and MaxapemR (Gist-Brocades);
and a and (3 amylases such as Purafect Ox AmR (Genencor) and TermamylR, BanR, FungamylR, DuramylR, and NatalaseR (Novo); and mixtures thereof. Enzymes are preferably added herein as prills, granulates, or cogranulates at levels typically in the range from about 0.0001% to about 2% pure enzyme by weight of composition.
Bleaching agent Bleaching agents suitable herein include chlorine and oxygen bleaches, especially inorganic perhydrate salts such as sodium perborate mono-and tetrahydrates and sodium percarbonate optionally coated to provide controlled rate of release (see, for example, GB-A-1466799 on sulfate/carbonate coatings), preformed organic peroxyacids and mixtures thereof with organic peroxyacid bleach precursors and/or transition metal-containing bleach catalysts (especially manganese or cobalt). Inorganic perhydrate salts are typically incorporated at levels in the range from about 1% to about 40% by weight, preferably from about 2% to about 30% by weight and more preferably from abut 5% to about 25%
by weight of composition. Peroxyacid bleach precursors preferred for use herein include precursors of perbenzoic acid and substituted perbenzoic acid; cationic peroxyacid precursors; peracetic acid precursors such as TAED, sodium acetoxybenzene sulfonate and pentaacetylglucose; pernonanoic acid precursors such as sodium 3,5,5-trimethylhexanoyloxybenzene sulfonate (iso-NOBS) and sodium nonanoyloxybenzene sulfonate (NOBS); amide substituted alkyl peroxyacid precursors (EP-A-0170386); and benzoxazin peroxyacid precursors (EP-A-0332294 and EP-A-0482807). Bleach p'recursors are typically incorporated at levels in the range from about 0.5%
to about 25%, preferably from about 1% to about 10% by weight of composition while the preformed organic peroxyacids themselves are typically incorporated at levels in the range from 0.5% to 25% by weight, more preferably from 1% to 10% by weight of composition.
Bleach catalysts preferred for use herein include the manganese triazacyclononane and related complexes (US-A-4246612, US-A-5227084); Co, Cu, Mn and Fe bispyridylamine and related complexes (US-A-5114611); and pentamine acetate cobalt(II) and related complexes(LTS-A-4810410).
Low cloud point non-ionic surfactants and suds suppressers The suds suppressers suitable for use herein include nonionic surfactants having a low cloud point. "Cloud point", as used herein, is a well known property of nonionic surfactants which is the result of the surfactant becoming less soluble with increasing temperature, the temperature at which the appearance of a second phase is observable is referred to as the "cloud point" (See Kirk Othmer, pp. 360-362). As used herein, a "low cloud point" nonionic surfactant is defined as a nonionic surfactant system ingredient having a cloud point of less than 30 C., preferably less than about 20 C., and even more preferably less than about 10 C., and most preferably less than about 7.5 C.
Typical low cloud point nonionic surfactants include nonionic alkoxylated surfactants, especially ethoxylates derived from primary alcohol, and polyoxypropylene/polyoxyethylene/polyoxypropylene (PO/EO/PO) reverse block polymers. Also, such low cloud point nonionic surfactants include, for example, ethoxylated-propoxylated alcohol (e.g., Olin Corporation's Poly-Tergent0 SLF18) and epoxy-capped poly(oxyalkylated) alcohols (e.g., Olin Corporation's Poly-Tergent0 SLF18B series of nonionics, as described, for example, in US-A-5,576,281).
Preferred low cloud point surfactants are the ether-capped poly(oxyalkylated) suds suppresser having the fonnula:
R10-(CH2 - i H -O)X - (CH2 -CH2 -O)y - (CH2 - i H-O)Z-H
wherein Rl is a linear, alkyl hydrocarbon having an average of from about 7 to about 12 carbon atoms, Rz is a linear, alkyl hydrocarbon of about 1 to about 4 carbon atoms, R3 is a linear, alkyl hydrocarbon of about 1 to about 4 carbon atoms, x is an integer of about 1 to about 6, y is an integer of about 4 to about 15, and z is an integer of about 4 to about 25.
Other low cloud point nonionic surfactants are the ether-capped poly(oxyalkylated) having the formula:
RIO(RIIO)nCH(CH3)ORm wherein, RI is selected from the group consisting of linear or branched, saturated or unsaturated, substituted or unsubstituted, aliphatic or aromatic hydrocarbon radicals having from about 7 to about 12 carbon atoms; RII may be the same or different, and is independently selected from the group consisting of branched or linear C2 to C7 alkylene in any given molecule; n is a number from 1 to about 30; and Rm is selected from the group consisting of (i) a 4 to 8 membered substituted, or unsubstituted heterocyclic ring containing from 1 to 3 hetero atoms; and (ii) linear or branched, saturated or unsaturated, substituted or unsubstituted, cyclic or acyclic, aliphatic or aromatic hydrocarbon radicals having from about 1 to about 30 carbon atoms;
(b) provided that when R2 is (ii) then either: (A) at least one of Rl is other than C2 to C3 alkylene; or (B) R2 has from 6 to 30 carbon atoms, and with the further proviso that when R2 has from 8 to 18 carbon atoms, R is other than Cl to Cs allcyl.
Other suitable components herein include organic polymers having dispersant, anti-redeposition, soil release or other detergency properties invention in levels of from about 0.1% to about 30%, preferably from about 0.5% to about 15%, most preferably from about 1% to about 10% by weight of composition. Preferred anti-redeposition polymers herein include acrylic acid containing polymers such as Sokalan pA30, PA20, PA15, PA10 and Sokalan CP10 (BASF GrmbH),Acusol 45N, 480N, 460N (Rohm and Haas), acrylic acid/maleic acid copolymers such as Sokalan CP5 and acrylic/methacrylic copolymers. Preferred soil release polymers herein include alkyl and hydroxyalkyl celluloses (IJS-A-4,000,093), polyoxyethylenes, polyoxypropylenes and copolymers thereof, and nonionic and anionic polymers based on terephthalate esters of ethylene glycol, propylene glycol and mixtures thereof.
Heavy metal sequestrants and crystal growth inhibitors are-suitable for use herein in levels generally from about 0.005% to about 20%, preferably from about 0.1% to about 10%, more preferably from about 0.25% to about 7.5% and most preferably from about 0.5% to about 5% by weight of composition, for example diethylenetriamine penta (methylene phosphonate), ethylenediamine tetra(methylene phosphonate) hexamethylenediamine tetra(methylene phosphonate), ethylene diphosphonate, hydroxy-ethylene-1,1-diphosphonate, nitrilotriacetate, ethylenediaminotetracetate, ethylenediamine-N,N'-disuccinate in their salt and free acid forms.
The compositions herein can contain a corrosion inhibitor such as organic silver coating agents in levels of from about 0.05% to about 10%, preferably from about 0.1%
to about 5% by weight of composition (especially paraffins such as Winog 70 sold by Wintershall, Salzbergen, Germany), nitrogen-containing corrosion inhibitor compounds (for example benzotriazole and benzimadazole - see GB-A 1137741) and Mn(D) compounds, particularly Mn(IC) salts of organic ligands in levels of from about 0.005% to about 5%, preferably from about 0.01% to about 1%, more preferably from about 0.02% to about 0.4% by weight of the composition.
Other suitable components herein include colorants, water-soluble bismuth compounds such as bismuth acetate and bismuth citrate at levels of from about 0.01% to about 5%, enzyme stabilizers such as calciuni ion, boric acid, propylene glycol and chlorine bleach scavengers at levels of from about 0.01% to about 6%, lime soap dispersants (see WO-A-93/08877), suds suppressors (see WO-93/08876 and EP-A-0705324), polymeric dye transfer inhibiting agents, optical brighteners, perfumes, fillers and clay.
Liquid detergent compositions can contain water and other volatile solvents as carriers.
Low quantities of low molecular weight primary or secondary alcohols such as methanol, ethanol, propanol and isopropanol can be used in the liquid detergent of the present invention. Other suitable carrier solvents used in low quantities includes glycerol, propylene glycol, ethylene glycol, 1,2-propanediol, sorbitol and mixtures thereof.
Examples Abbreviations used in Examples In the examples, the abbreviated component identifications have the following meanings:
Carbonate . Anhydrous sodium carbonate STPP . Sodium tripolyphosphate SKTP . Sodium potassium tripolyphosphate Silicate 3.2 : Amorphous Sodium Silicate (Si02:Na20 ratio = 3:2) Silicate : Amorphous Sodium Silicate (Si02:Na20 ratio = 2.0) SKS-6 . Crystalline layered silicate of formula 6-Na2Si205 KOH : Potassium hydroxide H2SO4 : Sulphuric acid HEDP . Ethane 1-hydroxy-1,1-diphosphonic acid PB1 . Sodium perborate monohydrate average particle size 770 m PB1-50 . Sodium perborate monohydrate average particle size 50 m Tennamyl . a-amylase available from Novo Nordisk A/S
FN3 : protease available from Genencor Savinase : protease available from Novo Nordisk A/S
LF404 : low foaming surfactant available from Olin Corporation SLF18 . low foaming surfactant available from Olin Corporation ACN! alkyl capped non-ionic surfactant of formula C9i11 H19rz3 EO$-cyclohexyl acetal C16A0 hexadecyl dimethyl amine oxide PA30 . Polyacrylate homo-polymer of molecular weight approximately 8,000 available from BASF
Proxel GXL : preservative(1,2-benzisothiazolin-3-one) available from Zeneca, Inc Polygel premix : 5% active Polygel DKP in water available from 3V Inc.
CaC12 . Calcium chlorine CHDM : Cyclohexane dimethanol BTA . Benzotriazole Winog : Paraffin oil sold by Wintershall.
Vivapurg : Microcrystalline cellulose of average particle size 0.18 mm Triacetate : Sodium acetate trihydrate Duramyl : a-amylase available from Novo Nordisk A/S
Citrate : Tripotassium citrate monohydrate Citric Acid : Anhydrous Citric acid Bicarbonate . Sodium hydrogen carbonate PEG 400 : Polyethylene Glycol molecular weight approximately 400 available from Hoechst PEG 4000. : Polyethylene Glycol molecular weight approximately 4000 available from Hoechst PVPVI : Polyvinylpyrrolidone vinylimidazole copolymer molecular weight approximately 15,000 available from BASF
MEA : Monoethanolamine MAE : 2-(methylamino)ethanol SF1488 . Polydimethylsiloxane copolymer Dowanol PNB , Propylene glycol butyl ether Silwet L7600 . Siloxane surfactant available from Witco In the following examples all levels are quoted as parts by weight.
Examples 1 to 5 A combination of solvent compositions and automatic dishwashing detergents are used to wash a load of tableware and cookware having cooked-on, baked-on and burnt-on food soils. The load comprises different soils and different substrates: lasagne baked for 2 hours at 140 C on Pyrex, lasagne cooked for 2 hours at 150 C on stainless steel, potato and cheese cooked for 2 hours at 150 C on stainless steel, egg yolk cooked for 2 hours at 150 C on stainless steel and sausage cooked for 1 hour at 120 C followed by 1 hour at 180 C. The load is washed in a 5 litre liquor capacity Bosch 6032 dishwashing machine, at 55 C without prewash, using the compositions given in Examples 1 to 5.
Examples 1 to 5 illustrate the use of a combination of a two-phase automatic dishwashing detergent tablet and an organic solvent composition added separately to the main-wash cycle of the dishwashing machine. The two-component compositions of examples 1 to 5 provided excellent removal of cooked-on, baked-on and burnt-on food soils.
Example 1 2 3 4 5 Dishwashing detergent com osp ition Phase 1 Carbonate 3.5 3.4 5.030 3.375 5.063 STPP 10.1 10.1 9.49 9.85 8.73 Silicate 1.1 1.0 1.58 1.61 1.548 SKS-6 1.5 1.4 2.16 1.425 2.138 HEDP 0.18 0.18 0.27 0.18 0.27 PB1 2.45 2.45 3.53 2.4 3.6 Termamyl 0.11 0.11 0.16 0.11 0.165 FN3 0.15 Savinase 0.12 0.12 0.17 0.12 0.18 LF404 0.60 0.60 0.86 SLF18 0.60 0.90 C16 AO 0.16 0.24 PA30 0.1 0.1 0.15 CHDM 0.02 0.03 BTA 0.06 0.03 0.09 0.045 0.068 PEG 4000 0.26 0.26 0.44 Winog 0.1 0.07 0.09 0.065 0.098 Vivapur 0.48 0.32 0.48 Triacetate 0.72 Perfume 0.02 0.02 0.01 Total 20.1g 19.84g 25.23g 21.05g 24.663g Phase 2 FN3 0.29 0.499 0.29 0.499 0.499 Termamyl 0.29 0.29 0.29 0.29 0.29 Citric acid 0.23 0.1 0.23 0.1 0.1 Bicarbonate 0.62 0.289 0.62 0.289 0.289 PEG 400 0.02 0.01 0.02 0.01 0.01' PEG 4000 0.07 0.2 0.07 0.2 0.2 PVPVI 0.095 0.095 0.095 Potassium Citrate 0.2 0.2 0.2 Total 1.52g 1.683g 1.52g 1.683g 1.683g Organic solvent composition Total 10 ml 10 ml 12 ml 10 ml 10 ml Examples 1 to 5 were repeated using the same automatic dishwashing detergent compositions but using an organic solvent composition comprising 10 ml of 2-amino-2-methyl-l-propanol and 2m1 of Silwet L7600. The compositions provided excellent removal of cooked-on, baked-on and burnt-on food soils.
Examples 6 to 10 Examples 6 to 10 illustrate the use of a combination of an automatic dishwashing liquid detergent and an organic solvent composition for removing cooked-, baked- and burnt-on soils. The two-component compositions of examples 6 to 10 are used to wash a load of cookware and tableware according to the procedure described hereinabove (Examples 1 to 5). 30 ml of the dishwashing detergent and the 10 ml of the solvent composition are separately delivered to the main-wash cycle of a 5 litre liquor capacity Bosch dishwashing machine, at 55 C without prewash. The compositions of examples 6 to 10 provide excellent removal of cooked-on, baked-on and burnt-on food soils.
Example 6 7 8 9 10 Dishwashing detergent com osp ition KOH 14.31 14.31 14.31 11.45 4.67 H2SO4 11.26 11.26 11.26 9.00 STPP 16.00 16.00 16.00 20.00 SKTP 30.00 1,2-Propanediol 0.50 0.50 0.50 0.5 6.00 Boric acid 3.00 3.00 3.00 3.0 4.00 Polygel premix 24.40 24.40 24.40 24.00 24.40 PVPVI 0.02 SLF18 1.0 1.0 1.00 C16 AO 0.6 0.6 2.00 2.00 ACNI 0.3 0.3 3.00 CaC12 0.04 0.04 0.04 0.37 0.37 Na benzoate 0.61 0.61 0.61 0.61 0.61 Proxel GXL 0.05 0.05 0.05 0.05 0.05 FN3 0.60 0.60 0.60 0.60 0.90 Duramyl 0.27 0.27 0.27 Termamyl 0.3 0.17 0.26 Perfume 0.1 0.1 0.2 0.1 0.1 Dye 0.4 0.4 0.3 0.24 0.64 Water to 100 Organic solvent composition Examples 6 to 10 were repeated using the same automatic dishwashing detergent compositions but using an organic solvent composition comprising 10 ml of 2-amino-2-methyl-l-propanol and 2m1 of Silwet L7600. The compositions provided excellent removal of cooked-on, baked-on and burnt-on food soils.
Examples 11 to 15 Examples 11 to 15 further illustrate the use of a combination of an automatic dishwashing liquid detergent and an organic solvent composition for removing cooked-, baked- and burnt-on soils. The two-component compositions of examples 11 to 15 are used to wash a load of cookware and tableware according to the procedure described hereinabove (Examples 1 to 5). The automatic dishwashing liquid detergent and the organic solvent composition are delivered in separate compartments of a unit dose (30 ml of the dishwashing detergent and the 10 ml of the solvent composition) partially hydrolysed PVA water-soluble pouch. The pouch is delivered to the main-wash cycle of a Bosch 6032 dishwashing machine, at 55 C without prewash. The two-component compositions of examples 11 to 15 provide excellent removal of cooked-on, baked-on and burnt-on food soils. At the same time, they provide excellent compatibility with the PVA pouch material.
Example 11 12 13 14 15 Dishwashing deter egnt composition KOH 14.31 14.31 14.31 11.45 4.67 H2SO4 11.26 11.26 11.26 9.00 STPP 16.00 16.00 16.00 20.00 SKTP 30.00 1,2-Propanediol 0.50 0.50 0.50 0.5 6.00 Boric acid 3.00 3.00 3.00 3.0 4.00 Polygel premix 24.40 24.40 24.40 24.00 24.40 PVPVI 0.02 SLF18 1.0 1.0 1.00 C16 AO 0.6 0.6 2.00 2.00 ACNI 0.3 0.3 3.00 CaC12 0.04 0.04 0.04 0.37 0.37 Na benzoate 0.61 0.61 0.61 0.61 0.61 Proxel GXL 0.05 0.05 0.05 0.05 0.05 FN3 0.60 0.60 0.60 0.60 0.90 Duramyl 0.27 0.27 0.27 Termamyl 0.3 0.17 0.26 Perfume 0.1 0.1 0.2 0.1 0.1 Dye 0.4 0.4 0.3 0.24 0.64 Water to 100 Organic solvent composition Benzyl alcohol 50 50 40 40 30 Examples 1 to 5 were repeated using the same automatic dishwashing detergent compositions but using an organic solvent composition comprising 10 ml of 2-amino-2-methyl-l-propanol and 2ml of Silwet L7600. The compositions provided excellent removal of cooked-on, baked-on and burnt-on food soils.
Examples 16 to 19 Examples 16 to 19 illustrate the use of a combination of an automatic dishwashing liquid detergent and an organic solvent composition for removing cooked-, baked- and burnt-on soils. The two-component compositions are stored in a dual-compartment bottle having an electrically operated pump and delivered at a feed ratio (dishwashing liquid detergent:
organic solvent composition) of 3:1. The compositions of examples 16 to 19 are used to wash a dishware load according to the procedure described hereinabove (Examples 1 to 5). 30 ml of the dishwashing detergent and 10 ml of the solvent composition are separately delivered from the dual-compartment bottle to the main-wash cycle of a Bosch 6032 dishwashing machine, at 55 C without prewash. The two-component compositions of examples 16 to 19 provide excellent removal of cooked-on, baked-on and burnt-on food soils. The above examples 16 to 19 were repeated using a dishwashing liquid detergent: organic solvent composition ratio of 4:1 with similar results.
Example 16 17 18 19 Dishwashing detergent composition STPP 28.00 28.00 28.00 28.00 KOH 5.30 5.30 5.30 5.30 Silicate 3.2 1.0 1.0 1.0 1.0 Polygel DKP 0.55 0.55 0.55 0.55 SLF18 1.25 1.25 C16 AO 0.40 0.40 ACNI 3.00 3.00 Water to 100 Organic solvent composition MEA 74.00 37.00 37.00 MAE 74.00 37.00 37.00 PB1-50 18.5 18.5 18.5 18.5 FN3 2.60 2.60 2.60 2.60 Termamyl 3.34 3.34 3.34 3.34 Thickener 1.56 1.56 1.56 1.56 Examples 20 to 24 Examples 20 to 24 illustrate "all-in-one" solvent-containing automatic dishwashing detergent compositions. The compositions of examples 20 to 24 are used to wash a dishware load following the procedure described hereinabove (Examples 1 to 5).
40 ml of the dishwashing composition are delivered to the main-wash cycle of a Bosch dishwashing machine, at 55 C without prewash. The "all-in-one" compositions of examples 20 to 24 provide excellent removal of baked-on soils.
Example 20 21 22 23 24 Dishwashing detergent solvent composition KOH 4.60 5.65 2.10 1.47 1.05 H2SO4 3.94 3.94 MEA 4.00 4.00 8.00 STPP 22.00 22.00 22.00 22.00 SKTP 30.00 1,2-Propanediol 0.5 0.5 6.00 5.5 5.5 Boric acid 3.00 3.00 4.00 3.4 3.4 Polygel premix 1.18 1.18 1.18 1.18 1.18 SLF18 1.0 1.0 ACNI 3.0 2.1 2.1 C16 AO 0.40 0.308 0.308 CaC12 0.2 0.2 0.22 0.2 0.2 Na benzoate 0.20 0.20 0.20 0.20 0.20 Proxel GXL 0.01 0.01 0.05 0.01 0.01 FN3 0.60 0.60 0.90 0.76 0.76 Duramyl 0.27 Termamyl 0.17 0.26 0.23 0.23 Perfume 0.10 0.10 0.10 0.10 0.10 Dye 0.0024 0.0024 0.0024 0.0024 0.0024 Water to 100
The invention also relates to detergent compositions suitable for use in automatic dishwashing or dishwashing pretreatment. In one embodiment, an automatic dishwashing detergent composition comprises from about 0.05% to about 10% by weight of a low-foaming non-ionic surfactant, from about 1% to about 30% of an organoamine, preferably alkanolarnine (especially monoethanolamine) solvent and at least about 5% by weight of a detergency builder. Preferably, the automatic dishwashing detergent composition is in the form of a gel comprising from about 2% to about 20%, preferably from 5% to 15%
by weight of an alkanolamine, at least about 5% by weight of detergency builder, and from about 0.1% to about 5% by weight of a low foaming non-ionic surfactant.
Although any non-ionic low foaming surfactant (or combination of non-ionic surfactants and suds suppressers) can be used herein, capped nonionic surfactants and combinations or amine oxide and capped non-ionic surfactants are preferred. The compositions also preferably have a pH (1% aqueous solution) in excess of about 9.0, preferably in excess of about 10.5 and more preferably greater than about 11.
In one embodiment, an automatic dishwashing detergent composition comprises from about 0.05% to about 10% by weight of a low-foaming non-ionic surfactant, from about 1% to about 30% of an organic solvent, preferably alkanolamine solvent, at least about 5% by weight of a detergency builder and a wetting agent, preferably a silicone-poly(alkyleneoxide) copolymers.
In a preferred embodiment an automatic dishwashing detergent pack is provided, comprising: i) an organic solvent composition suitable for use in automatic dishwashing comprising from about 1% to about 99%, preferably from about 5% to about 90%, especially from about 40% to about 80% of an organic solvent system for removing cooked-, baked-, or burnt-on food soil from cookware and tableware, from about 0.5% to about 50%, preferably from about 5% to about 25% of bleach, from about 0.0001%
to about 10% of detergency enzyme, and wherein the composition is in the form of an anhydrous gel comprising bleach in the form of a particulate suspension; and ii) an automatic dishwashing detergent composition comprising from about 0.05% to about 10% by weight of a low-foaming non-ionic surfactant, optionally from about 1%
to about 30% of an organoamine, preferably alkanolamine solvent, and at least about 5%
by weight of a detergency builder. Preferably, the automatic dishwashing detergent composition is in the form of a gel comprising from about 2% to about 20%, preferably from about 5% to about 15% by weight of the composition of an alkanolamine, at least about 5%
by weight of detergency builder (such as sodium potassium tripolyphosphate), and from about 0.1%
to about 5% by weight of the composition of a low foaming non-ionic surfactant.
The compositions of the invention are also characterised by having a low volatile organic content, preferably with a volatile organic content less than about 20%, preferably less than about 10% and more preferably less than about 5%.
Suitable thickening agents for use in the solvent compositions and dishwashing detergent compositions herein include viscoelastic, thixotropic thickening agents at levels of from about 0.1% to about 10%, preferably from about 0.25% to about 5%, most preferably from about 0.5% to about 3% by weight. Suitable thickening agents include polymers with a molecular weight from about 500,000 to about 10,000,000, more preferably from about 750,000 to about 4,000,000. The preferred cross-linked polycarboxylate polymer is preferably a carboxyvinyl polymer. Such compounds are disclosed in U.S. Pat.
No.
2,798,053, issued on Jul. 2, 1957, to Brown. Methods for making carboxyvinyl polymers are also disclosed in Brown. Carboxyvinyl polymers are substantially insoluble in liquid, volatile organic hydrocarbons and are dimensionally stable on exposure to air.
Preferred polyhydric alcohols used to produce carboxyvinyl polymers include polyols selected from the class consisting of oligosaccarides, reduced derivatives thereof in which the carbonyl group is converted to an alcohol group, an pentaerythritol; most preferred is sucrose or pentaerythritol. It is preferred that the hydroxyl groups of the modified polyol be etherified with alkyl groups, the polyol having at least two allyl ether groups per polyol molecule. When the polyol is sucrose, it is preferred that the sucrose have at least about five allyl ether groups per sucrose molecule. It is preferred that the polyether of the polyol comprise from about 0.1% to about 4% of the total monomers, more preferably from about 0.2% to about 2.5%.
Preferred monomeric olefinically unsaturated carboxylic acids for use in producing carboxyvinyl polymers used herein include monomeric, polymerizable, alpha-beta monoolefinically unsaturated lower aliphatic carboxylic acids; more preferred are monomeric monoolefinic acrylic acids of the structure:
CHCH2=C(R)-COOH
where R is a substituent selected from the group consisting of hydrogen and lower alkyl groups; most preferred is acrylic acid.
Various carboxyvinyl polymers, homopolymers and copolymers are commercially available from B. F. Goodrich Company, New York, N.Y., under the trade name Carbopol0. These polymers are also known as carbomers or polyacrylic acids.
Carboxyvinyl polymers useful in formulations of the present invention include Carbopol 910 having a molecular weight of about 750,000, Carbopol 941 having a molecular weight of about 1,250,000, and Carbopols 934 and 940 having molecular weights of about 3,000,000 and 4,000,000, respectively. More preferred are the series of Carbopols which use ethyl acetate and cyclohexane in the manufacturing process, Carbopol 981, 2984, 980, and 1382.
Preferred polycarboxylate polymers are non-linear, water-dispersible, polyacrylic acid cross-linked with a polyalkenyl polyether and having a molecular weight of from about 750,000 to about 4,000,000.
Highly preferred examples of these polycarboxylate polymers for use in the present invention are Sokalan PHC-25 , a polyacrylic acid available from BASF
Corporation, the Carbopol 600 series resins available from B. F. Goodrich, and more preferred is Polygel DK available from 3-V Chemical Corporation. Mixtures of polycarboxylate polymers as herein described may also be used in the present invention.
Other suitable thickening agents include inorganic clays (e.g. laponites, aluminium silicate, bentonite, fumed silica). The preferred clay thickening agent can be either naturalIy occurring or synthetic. Preferred synthetic clays include the synthetic smectite-type clay sold under the trademark Laponite by Southern Clay Products, Inc.
Particularly useful are gel forming grades such as Laponite RD and sol forming grades such as Laponite RDS. Natural occumng clays include some smectite and attapulgite clays.
Mixtures of clays and polymeric thickeners are also suitable for use herein.
Other types of thickeners which can be used in this composition include natural gums, such as xanthan gum, locust bean gum, guar gum, and the like. The cellulosic type thickeners: hydroxyethyl and hydroxymethyl cellulose (ETHOCEL and METHOCEL
available from Dow Chemical) can also be used.
It is a feature of the invention that many of the solvent systems and compositions of the invention that are optimum for cleaning also demonstrate improved compatibility with partially hydrolysed PVA pouch materials of known construction and type. This is particularly surprising given that many well-known polar/or hydrolysed bonding solvent materials (for example the ethanolamines) in themselves have low compatibility with PVA materials and present serious issues for product stability. Solvent systems comprising mixtures of polar hydrogen bonding solvents (such as the organoamines) with a cosolvent selected from polar non-hydrogen bonding, amphiphilic and non-polar solvents and mixtures thereof are particularly valuable in this respect. Also valuable for improved PVA compatibility are organoamines present in composition in the form of amine salt. Also valuable for improved PVA compatibility are solvent systems and components based on propanolamines such as 2-amino-2-methyl propanol.
Compositions suitable for inclusion in pouches will normally comprise a major proportion of solvent system components, preferably at least 50% by weight, more preferably at least 70% by weight or even higher.
Detailed description of the invention The present invention envisages the use of plurality of compositions including at least one organic solvent composition into the same or different cycles of an automatic dishwashing machine and washing the soiled cookware/tableware in the resulting solvent-containing wash liquor. It also envisages multi-component dishwashing products containing purpose-designated combination of solvent compositions and dishwashing detergent compositions. The invention also envisages so called "all-in-one" detergent products having both an alkaline detergent and a solvent functionality. In the case of additive and multi-component products, the invention does not require the two compositions to be in the same physical form. The organic solvent composition can be in any physical form, e.g. liquid, paste, cream, gel, powder, granules or tablets and similarly the automatic dishwashing detergent composition can be in any of these forms. Preferably, however, both compositions are in the form of liquids or gels or the organic solvent composition is in the form of liquid or gel and the automatic dishwashing detergent composition is in the form of powder, granules or tablet. The compositions used herein can be dispensed from any suitable device, such as bottles (pump assisted bottles, squeeze bottles), paste dispensers, capsules, multi-compartment bottles, multi-compartment capsules, pouches, and multi-compartment pouches, etc.
The solvent compositions herein comprise one or more organic solvents and can additionally comprises surfactant, bleach, enzyme, enzyme stabilising components, thickener, etc.
The organic solvents should be selected so as to be compatible with the tableware/cookware as well as with the different parts of an automatic dishwashing machine. Furthermore, the solvent system should be effective and safe to use having a volatile organic content above 1 mm Hg (and preferably above 0.1 mm Hg) of less than about 50%, preferably less than about 30%, more preferably less than about 10%
by weight of the solvent system. Also they should have very mild pleasant odours.
The individual organic solvents used herein generally have a boiling point above about 150 C,.
flash point above about 100 C and vapor pressure below about 1 mm Hg, preferably below 0.1 mm Hg at 25 C and atmospheric pressure.
Solvents that can be used herein include: i) alcohols, such as benzyl alcohol, 1,4-cyclohexanedimethanol, 2-ethyl-l-hexanol, furfuryl alcohol, 1,2-hexanediol and other similar materials; ii) amines, such as alkanolamines (e.g. primary alkanolamines:
monoethanolamine, monoisopropanolamine, diethylethanolamine, ethyl diethanolamine, beta-aminoalkanols; secondary alkanolamines: diethanolamine, diisopropanolamine, 2-(methylamino)ethanol; ternary alkanolamines: triethanolamine, triisopropanolamine);
alkylamines (e.g. primary alkylamines: monomethylamine, monoethylamine, monopropylamine, monobutylamine, monopentylamine, cyclohexylamine), secondary alkylamines: (dimethylamine), alkylene amines (primary alkylene amines:
ethylenediamine, propylenediamine) and other similar materials; iii) esters, such as ethyl lactate, methyl ester, ethyl acetoacetate, ethylene glycol monobutyl ether acetate, diethylene glycol monoethyl ether acetate, diethylene glycol monobutyl ether acetate and other similar materials; iv) glycol ethers, such as ethylene glycol monobutyl ether, diethylene glycol monobutyl ether, ethylene glycol monomethyl ether, ethylene glycol monoethyl ether, diethylene glycol monomethyl ether, diethylene glycol monoethyl ether, propylene glycol butyl ether and other similar materials; v) glycols, such as propylene glycol, diethylene glycol, hexylene glycol (2-methyl-2, 4 pentanediol), triethylene glycol, composition and dipropylene glycol and other similar materials; and mixtures thereof.
Preferred solvents effective in removing cooked-, baked- or burnt-on food soil to be used herein coinprise alkanolamines, especially monoethanolamine, beta-aminoalkanols, especially 2-amino-2-methyl-propanol (since it has the lowest molecular weight of any beta-aminoalkanol which has the amine group attached to a tertiary carbon, therefore minimize the reactivity of the amine group) and mixtures thereof.
The detergent and cleaning compositions herein can comprise traditional detergency components and can also comprise organic solvents having a cleaning function and organic solvents having a carrier or diluent function or some other specialised function.
The cornpositions will generally be built and comprise one or more detergent active components which may be selected from colorants, bleaching agents, surfactants, alkalinity sources, enzymes, thickeners (in the case of liquid, paste, cream or gel compositions), anti-corrosion agents (e.g. sodium silicate), hydrotropes (e.g.
sodium cumene sulfate) and disrupting and binding agents (in the case of powder, granules or tablets). Highly preferred detergent components include a builder compound, an alkalinity source, a surfactant, an enzyme and a bleaching agent.
Unless otherwise specified, the components described hereinbelow can be incorporated either in the organic solvent compositions and/or the detergent or cleaning compositions.
Surfactant In the methods of the present invention for use in automatic dishwashing the detergent surfactant is preferably low foaming by itself or in combination with other components (i.e. suds suppressers). In compositions and methods of the present invention for use in hard surface cleaning or pretreatment prior to dishwashing, the detergent surfactant is preferably foamable in direct application but low foaming in automatic dishwashing use.
Surfactants suitable herein include anionic surfactants such as alkyl sulfates, alkyl ether sulfates, alkyl benzene sulfonates, alkyl glyceryl sulfonates, alkyl and alkenyl sulphonates, alkyl ethoxy carboxylates, N-acyl sarcosinates, N-acyl taurates and alkyl succinates and sulfosuccinates, wherein the alkyl, alkenyl or acyl moiety is C5-C20 , preferably C10-C18 linear or branched; cationic surfactants such as chlorine esters (US-A-4228042, US-A-4239660 and US-A-4260529) and mono C6-C16 N-alkyl or alkenyl ammonium surfactants wherein the remaining N positions are substituted by methyl, hydroxyethyl or hydroxypropyl groups; low and high cloud point nonionic surfactants and mixtures thereof including nonionic alkoxylated surfactants (especially ethoxylates derived from C6-C18 primary alcohols), ethoxylated-propoxylated alcohols (e.g., Olin Corporation's Poly-Tergent SLF18), epoxy-capped poly(oxyalkylated) alcohols (e.g., Olin Corporation's Poly-Tergent SLF18B - see WO-A-94/22800), ether-capped poly(oxyalkylated) alcohol surfactants, and block polyoxyethylene-polyoxypropylene polymeric compounds such as PLURONICO, REVERSED PLURONICO, and TETRONICO by the BASF-Wyandotte Corp., Wyandotte, Michigan; amphoteric surfactants such as the C12-C20 alkyl amine oxides (preferred ainine oxides for use herein include lauryldimethyl amine oxide and hexadecyl dimethyl amine oxide), and alkyl amphocarboxylic surfactants such as MiranolTM C2M; and zwitterionic surfactants such as the betaines and sultaines; and mixtures thereof. Surfactants suitable herein are disclosed, for example, in US-A-3,929,678 , US-A- 4,259,217, EP-A-0414 549, WO-A-93/08876 and WO-A-93/08874. Surfactants are typically present at a level of from about 0.2% to about 30% by weight, more preferably from about 0.5% to about 10% by weight, most preferably from about 1% to about 5% by weight of composition. Preferred surfactant for use herein are low foaming and include low cloud point nonionic surfactants and mixtures of higher foaming surfactants with low cloud point nonionic surfactants which act as suds suppresser therefor.
Builder Builders suitable for use herein include water-soluble builders such as citrates, carbonates and polyphosphates e.g. sodium tripolyphosphate and sodium tripolyphosphate hexahydrate, potassium tripolyphosphate and mixed sodium and potassium tripolyphosphate salts; and partially water-soluble or insoluble builders such as crystalline layered silicates (EP-A-0164514 and EP-A-0293640) and aluminosilicates inclusive of Zeolites A, B, P, X, HS and MAP. The builder is typically present at a level of from about 1% to about 80% by weight, preferably from about 10% to about 70% by weight, most preferably from about 20% to about 60% by weight of composition.
Amorphous sodium silicates having an Si02:Na20 ratio of from 1.8 to 3.0, preferably from 1.8 to 2.4, most preferably 2.0 can also be used herein although highly preferred from the viewpoint of long term storage stability are compositions containing less than about 22%, preferably less than about 15% total (amorphous and crystalline) silicate.
Enzyme Enzymes suitable herein include bacterial and fungal cellulases such as Carezyme and Celluzyme (Novo Nordisk A/S); peroxidases; lipases such as Amano-P (Amano Pharmaceutical Co.), Ml LipaseR and LipomaxR (Gist-Brocades) and LipolaseR and Lipolase UltraR (Novo); cutinases; proteases such as EsperaseR, AlcalaseR, DurazymR and SavinaseR (Novo) and MaxataseR, Maxacali ; ProperaseR and MaxapemR (Gist-Brocades);
and a and (3 amylases such as Purafect Ox AmR (Genencor) and TermamylR, BanR, FungamylR, DuramylR, and NatalaseR (Novo); and mixtures thereof. Enzymes are preferably added herein as prills, granulates, or cogranulates at levels typically in the range from about 0.0001% to about 2% pure enzyme by weight of composition.
Bleaching agent Bleaching agents suitable herein include chlorine and oxygen bleaches, especially inorganic perhydrate salts such as sodium perborate mono-and tetrahydrates and sodium percarbonate optionally coated to provide controlled rate of release (see, for example, GB-A-1466799 on sulfate/carbonate coatings), preformed organic peroxyacids and mixtures thereof with organic peroxyacid bleach precursors and/or transition metal-containing bleach catalysts (especially manganese or cobalt). Inorganic perhydrate salts are typically incorporated at levels in the range from about 1% to about 40% by weight, preferably from about 2% to about 30% by weight and more preferably from abut 5% to about 25%
by weight of composition. Peroxyacid bleach precursors preferred for use herein include precursors of perbenzoic acid and substituted perbenzoic acid; cationic peroxyacid precursors; peracetic acid precursors such as TAED, sodium acetoxybenzene sulfonate and pentaacetylglucose; pernonanoic acid precursors such as sodium 3,5,5-trimethylhexanoyloxybenzene sulfonate (iso-NOBS) and sodium nonanoyloxybenzene sulfonate (NOBS); amide substituted alkyl peroxyacid precursors (EP-A-0170386); and benzoxazin peroxyacid precursors (EP-A-0332294 and EP-A-0482807). Bleach p'recursors are typically incorporated at levels in the range from about 0.5%
to about 25%, preferably from about 1% to about 10% by weight of composition while the preformed organic peroxyacids themselves are typically incorporated at levels in the range from 0.5% to 25% by weight, more preferably from 1% to 10% by weight of composition.
Bleach catalysts preferred for use herein include the manganese triazacyclononane and related complexes (US-A-4246612, US-A-5227084); Co, Cu, Mn and Fe bispyridylamine and related complexes (US-A-5114611); and pentamine acetate cobalt(II) and related complexes(LTS-A-4810410).
Low cloud point non-ionic surfactants and suds suppressers The suds suppressers suitable for use herein include nonionic surfactants having a low cloud point. "Cloud point", as used herein, is a well known property of nonionic surfactants which is the result of the surfactant becoming less soluble with increasing temperature, the temperature at which the appearance of a second phase is observable is referred to as the "cloud point" (See Kirk Othmer, pp. 360-362). As used herein, a "low cloud point" nonionic surfactant is defined as a nonionic surfactant system ingredient having a cloud point of less than 30 C., preferably less than about 20 C., and even more preferably less than about 10 C., and most preferably less than about 7.5 C.
Typical low cloud point nonionic surfactants include nonionic alkoxylated surfactants, especially ethoxylates derived from primary alcohol, and polyoxypropylene/polyoxyethylene/polyoxypropylene (PO/EO/PO) reverse block polymers. Also, such low cloud point nonionic surfactants include, for example, ethoxylated-propoxylated alcohol (e.g., Olin Corporation's Poly-Tergent0 SLF18) and epoxy-capped poly(oxyalkylated) alcohols (e.g., Olin Corporation's Poly-Tergent0 SLF18B series of nonionics, as described, for example, in US-A-5,576,281).
Preferred low cloud point surfactants are the ether-capped poly(oxyalkylated) suds suppresser having the fonnula:
R10-(CH2 - i H -O)X - (CH2 -CH2 -O)y - (CH2 - i H-O)Z-H
wherein Rl is a linear, alkyl hydrocarbon having an average of from about 7 to about 12 carbon atoms, Rz is a linear, alkyl hydrocarbon of about 1 to about 4 carbon atoms, R3 is a linear, alkyl hydrocarbon of about 1 to about 4 carbon atoms, x is an integer of about 1 to about 6, y is an integer of about 4 to about 15, and z is an integer of about 4 to about 25.
Other low cloud point nonionic surfactants are the ether-capped poly(oxyalkylated) having the formula:
RIO(RIIO)nCH(CH3)ORm wherein, RI is selected from the group consisting of linear or branched, saturated or unsaturated, substituted or unsubstituted, aliphatic or aromatic hydrocarbon radicals having from about 7 to about 12 carbon atoms; RII may be the same or different, and is independently selected from the group consisting of branched or linear C2 to C7 alkylene in any given molecule; n is a number from 1 to about 30; and Rm is selected from the group consisting of (i) a 4 to 8 membered substituted, or unsubstituted heterocyclic ring containing from 1 to 3 hetero atoms; and (ii) linear or branched, saturated or unsaturated, substituted or unsubstituted, cyclic or acyclic, aliphatic or aromatic hydrocarbon radicals having from about 1 to about 30 carbon atoms;
(b) provided that when R2 is (ii) then either: (A) at least one of Rl is other than C2 to C3 alkylene; or (B) R2 has from 6 to 30 carbon atoms, and with the further proviso that when R2 has from 8 to 18 carbon atoms, R is other than Cl to Cs allcyl.
Other suitable components herein include organic polymers having dispersant, anti-redeposition, soil release or other detergency properties invention in levels of from about 0.1% to about 30%, preferably from about 0.5% to about 15%, most preferably from about 1% to about 10% by weight of composition. Preferred anti-redeposition polymers herein include acrylic acid containing polymers such as Sokalan pA30, PA20, PA15, PA10 and Sokalan CP10 (BASF GrmbH),Acusol 45N, 480N, 460N (Rohm and Haas), acrylic acid/maleic acid copolymers such as Sokalan CP5 and acrylic/methacrylic copolymers. Preferred soil release polymers herein include alkyl and hydroxyalkyl celluloses (IJS-A-4,000,093), polyoxyethylenes, polyoxypropylenes and copolymers thereof, and nonionic and anionic polymers based on terephthalate esters of ethylene glycol, propylene glycol and mixtures thereof.
Heavy metal sequestrants and crystal growth inhibitors are-suitable for use herein in levels generally from about 0.005% to about 20%, preferably from about 0.1% to about 10%, more preferably from about 0.25% to about 7.5% and most preferably from about 0.5% to about 5% by weight of composition, for example diethylenetriamine penta (methylene phosphonate), ethylenediamine tetra(methylene phosphonate) hexamethylenediamine tetra(methylene phosphonate), ethylene diphosphonate, hydroxy-ethylene-1,1-diphosphonate, nitrilotriacetate, ethylenediaminotetracetate, ethylenediamine-N,N'-disuccinate in their salt and free acid forms.
The compositions herein can contain a corrosion inhibitor such as organic silver coating agents in levels of from about 0.05% to about 10%, preferably from about 0.1%
to about 5% by weight of composition (especially paraffins such as Winog 70 sold by Wintershall, Salzbergen, Germany), nitrogen-containing corrosion inhibitor compounds (for example benzotriazole and benzimadazole - see GB-A 1137741) and Mn(D) compounds, particularly Mn(IC) salts of organic ligands in levels of from about 0.005% to about 5%, preferably from about 0.01% to about 1%, more preferably from about 0.02% to about 0.4% by weight of the composition.
Other suitable components herein include colorants, water-soluble bismuth compounds such as bismuth acetate and bismuth citrate at levels of from about 0.01% to about 5%, enzyme stabilizers such as calciuni ion, boric acid, propylene glycol and chlorine bleach scavengers at levels of from about 0.01% to about 6%, lime soap dispersants (see WO-A-93/08877), suds suppressors (see WO-93/08876 and EP-A-0705324), polymeric dye transfer inhibiting agents, optical brighteners, perfumes, fillers and clay.
Liquid detergent compositions can contain water and other volatile solvents as carriers.
Low quantities of low molecular weight primary or secondary alcohols such as methanol, ethanol, propanol and isopropanol can be used in the liquid detergent of the present invention. Other suitable carrier solvents used in low quantities includes glycerol, propylene glycol, ethylene glycol, 1,2-propanediol, sorbitol and mixtures thereof.
Examples Abbreviations used in Examples In the examples, the abbreviated component identifications have the following meanings:
Carbonate . Anhydrous sodium carbonate STPP . Sodium tripolyphosphate SKTP . Sodium potassium tripolyphosphate Silicate 3.2 : Amorphous Sodium Silicate (Si02:Na20 ratio = 3:2) Silicate : Amorphous Sodium Silicate (Si02:Na20 ratio = 2.0) SKS-6 . Crystalline layered silicate of formula 6-Na2Si205 KOH : Potassium hydroxide H2SO4 : Sulphuric acid HEDP . Ethane 1-hydroxy-1,1-diphosphonic acid PB1 . Sodium perborate monohydrate average particle size 770 m PB1-50 . Sodium perborate monohydrate average particle size 50 m Tennamyl . a-amylase available from Novo Nordisk A/S
FN3 : protease available from Genencor Savinase : protease available from Novo Nordisk A/S
LF404 : low foaming surfactant available from Olin Corporation SLF18 . low foaming surfactant available from Olin Corporation ACN! alkyl capped non-ionic surfactant of formula C9i11 H19rz3 EO$-cyclohexyl acetal C16A0 hexadecyl dimethyl amine oxide PA30 . Polyacrylate homo-polymer of molecular weight approximately 8,000 available from BASF
Proxel GXL : preservative(1,2-benzisothiazolin-3-one) available from Zeneca, Inc Polygel premix : 5% active Polygel DKP in water available from 3V Inc.
CaC12 . Calcium chlorine CHDM : Cyclohexane dimethanol BTA . Benzotriazole Winog : Paraffin oil sold by Wintershall.
Vivapurg : Microcrystalline cellulose of average particle size 0.18 mm Triacetate : Sodium acetate trihydrate Duramyl : a-amylase available from Novo Nordisk A/S
Citrate : Tripotassium citrate monohydrate Citric Acid : Anhydrous Citric acid Bicarbonate . Sodium hydrogen carbonate PEG 400 : Polyethylene Glycol molecular weight approximately 400 available from Hoechst PEG 4000. : Polyethylene Glycol molecular weight approximately 4000 available from Hoechst PVPVI : Polyvinylpyrrolidone vinylimidazole copolymer molecular weight approximately 15,000 available from BASF
MEA : Monoethanolamine MAE : 2-(methylamino)ethanol SF1488 . Polydimethylsiloxane copolymer Dowanol PNB , Propylene glycol butyl ether Silwet L7600 . Siloxane surfactant available from Witco In the following examples all levels are quoted as parts by weight.
Examples 1 to 5 A combination of solvent compositions and automatic dishwashing detergents are used to wash a load of tableware and cookware having cooked-on, baked-on and burnt-on food soils. The load comprises different soils and different substrates: lasagne baked for 2 hours at 140 C on Pyrex, lasagne cooked for 2 hours at 150 C on stainless steel, potato and cheese cooked for 2 hours at 150 C on stainless steel, egg yolk cooked for 2 hours at 150 C on stainless steel and sausage cooked for 1 hour at 120 C followed by 1 hour at 180 C. The load is washed in a 5 litre liquor capacity Bosch 6032 dishwashing machine, at 55 C without prewash, using the compositions given in Examples 1 to 5.
Examples 1 to 5 illustrate the use of a combination of a two-phase automatic dishwashing detergent tablet and an organic solvent composition added separately to the main-wash cycle of the dishwashing machine. The two-component compositions of examples 1 to 5 provided excellent removal of cooked-on, baked-on and burnt-on food soils.
Example 1 2 3 4 5 Dishwashing detergent com osp ition Phase 1 Carbonate 3.5 3.4 5.030 3.375 5.063 STPP 10.1 10.1 9.49 9.85 8.73 Silicate 1.1 1.0 1.58 1.61 1.548 SKS-6 1.5 1.4 2.16 1.425 2.138 HEDP 0.18 0.18 0.27 0.18 0.27 PB1 2.45 2.45 3.53 2.4 3.6 Termamyl 0.11 0.11 0.16 0.11 0.165 FN3 0.15 Savinase 0.12 0.12 0.17 0.12 0.18 LF404 0.60 0.60 0.86 SLF18 0.60 0.90 C16 AO 0.16 0.24 PA30 0.1 0.1 0.15 CHDM 0.02 0.03 BTA 0.06 0.03 0.09 0.045 0.068 PEG 4000 0.26 0.26 0.44 Winog 0.1 0.07 0.09 0.065 0.098 Vivapur 0.48 0.32 0.48 Triacetate 0.72 Perfume 0.02 0.02 0.01 Total 20.1g 19.84g 25.23g 21.05g 24.663g Phase 2 FN3 0.29 0.499 0.29 0.499 0.499 Termamyl 0.29 0.29 0.29 0.29 0.29 Citric acid 0.23 0.1 0.23 0.1 0.1 Bicarbonate 0.62 0.289 0.62 0.289 0.289 PEG 400 0.02 0.01 0.02 0.01 0.01' PEG 4000 0.07 0.2 0.07 0.2 0.2 PVPVI 0.095 0.095 0.095 Potassium Citrate 0.2 0.2 0.2 Total 1.52g 1.683g 1.52g 1.683g 1.683g Organic solvent composition Total 10 ml 10 ml 12 ml 10 ml 10 ml Examples 1 to 5 were repeated using the same automatic dishwashing detergent compositions but using an organic solvent composition comprising 10 ml of 2-amino-2-methyl-l-propanol and 2m1 of Silwet L7600. The compositions provided excellent removal of cooked-on, baked-on and burnt-on food soils.
Examples 6 to 10 Examples 6 to 10 illustrate the use of a combination of an automatic dishwashing liquid detergent and an organic solvent composition for removing cooked-, baked- and burnt-on soils. The two-component compositions of examples 6 to 10 are used to wash a load of cookware and tableware according to the procedure described hereinabove (Examples 1 to 5). 30 ml of the dishwashing detergent and the 10 ml of the solvent composition are separately delivered to the main-wash cycle of a 5 litre liquor capacity Bosch dishwashing machine, at 55 C without prewash. The compositions of examples 6 to 10 provide excellent removal of cooked-on, baked-on and burnt-on food soils.
Example 6 7 8 9 10 Dishwashing detergent com osp ition KOH 14.31 14.31 14.31 11.45 4.67 H2SO4 11.26 11.26 11.26 9.00 STPP 16.00 16.00 16.00 20.00 SKTP 30.00 1,2-Propanediol 0.50 0.50 0.50 0.5 6.00 Boric acid 3.00 3.00 3.00 3.0 4.00 Polygel premix 24.40 24.40 24.40 24.00 24.40 PVPVI 0.02 SLF18 1.0 1.0 1.00 C16 AO 0.6 0.6 2.00 2.00 ACNI 0.3 0.3 3.00 CaC12 0.04 0.04 0.04 0.37 0.37 Na benzoate 0.61 0.61 0.61 0.61 0.61 Proxel GXL 0.05 0.05 0.05 0.05 0.05 FN3 0.60 0.60 0.60 0.60 0.90 Duramyl 0.27 0.27 0.27 Termamyl 0.3 0.17 0.26 Perfume 0.1 0.1 0.2 0.1 0.1 Dye 0.4 0.4 0.3 0.24 0.64 Water to 100 Organic solvent composition Examples 6 to 10 were repeated using the same automatic dishwashing detergent compositions but using an organic solvent composition comprising 10 ml of 2-amino-2-methyl-l-propanol and 2m1 of Silwet L7600. The compositions provided excellent removal of cooked-on, baked-on and burnt-on food soils.
Examples 11 to 15 Examples 11 to 15 further illustrate the use of a combination of an automatic dishwashing liquid detergent and an organic solvent composition for removing cooked-, baked- and burnt-on soils. The two-component compositions of examples 11 to 15 are used to wash a load of cookware and tableware according to the procedure described hereinabove (Examples 1 to 5). The automatic dishwashing liquid detergent and the organic solvent composition are delivered in separate compartments of a unit dose (30 ml of the dishwashing detergent and the 10 ml of the solvent composition) partially hydrolysed PVA water-soluble pouch. The pouch is delivered to the main-wash cycle of a Bosch 6032 dishwashing machine, at 55 C without prewash. The two-component compositions of examples 11 to 15 provide excellent removal of cooked-on, baked-on and burnt-on food soils. At the same time, they provide excellent compatibility with the PVA pouch material.
Example 11 12 13 14 15 Dishwashing deter egnt composition KOH 14.31 14.31 14.31 11.45 4.67 H2SO4 11.26 11.26 11.26 9.00 STPP 16.00 16.00 16.00 20.00 SKTP 30.00 1,2-Propanediol 0.50 0.50 0.50 0.5 6.00 Boric acid 3.00 3.00 3.00 3.0 4.00 Polygel premix 24.40 24.40 24.40 24.00 24.40 PVPVI 0.02 SLF18 1.0 1.0 1.00 C16 AO 0.6 0.6 2.00 2.00 ACNI 0.3 0.3 3.00 CaC12 0.04 0.04 0.04 0.37 0.37 Na benzoate 0.61 0.61 0.61 0.61 0.61 Proxel GXL 0.05 0.05 0.05 0.05 0.05 FN3 0.60 0.60 0.60 0.60 0.90 Duramyl 0.27 0.27 0.27 Termamyl 0.3 0.17 0.26 Perfume 0.1 0.1 0.2 0.1 0.1 Dye 0.4 0.4 0.3 0.24 0.64 Water to 100 Organic solvent composition Benzyl alcohol 50 50 40 40 30 Examples 1 to 5 were repeated using the same automatic dishwashing detergent compositions but using an organic solvent composition comprising 10 ml of 2-amino-2-methyl-l-propanol and 2ml of Silwet L7600. The compositions provided excellent removal of cooked-on, baked-on and burnt-on food soils.
Examples 16 to 19 Examples 16 to 19 illustrate the use of a combination of an automatic dishwashing liquid detergent and an organic solvent composition for removing cooked-, baked- and burnt-on soils. The two-component compositions are stored in a dual-compartment bottle having an electrically operated pump and delivered at a feed ratio (dishwashing liquid detergent:
organic solvent composition) of 3:1. The compositions of examples 16 to 19 are used to wash a dishware load according to the procedure described hereinabove (Examples 1 to 5). 30 ml of the dishwashing detergent and 10 ml of the solvent composition are separately delivered from the dual-compartment bottle to the main-wash cycle of a Bosch 6032 dishwashing machine, at 55 C without prewash. The two-component compositions of examples 16 to 19 provide excellent removal of cooked-on, baked-on and burnt-on food soils. The above examples 16 to 19 were repeated using a dishwashing liquid detergent: organic solvent composition ratio of 4:1 with similar results.
Example 16 17 18 19 Dishwashing detergent composition STPP 28.00 28.00 28.00 28.00 KOH 5.30 5.30 5.30 5.30 Silicate 3.2 1.0 1.0 1.0 1.0 Polygel DKP 0.55 0.55 0.55 0.55 SLF18 1.25 1.25 C16 AO 0.40 0.40 ACNI 3.00 3.00 Water to 100 Organic solvent composition MEA 74.00 37.00 37.00 MAE 74.00 37.00 37.00 PB1-50 18.5 18.5 18.5 18.5 FN3 2.60 2.60 2.60 2.60 Termamyl 3.34 3.34 3.34 3.34 Thickener 1.56 1.56 1.56 1.56 Examples 20 to 24 Examples 20 to 24 illustrate "all-in-one" solvent-containing automatic dishwashing detergent compositions. The compositions of examples 20 to 24 are used to wash a dishware load following the procedure described hereinabove (Examples 1 to 5).
40 ml of the dishwashing composition are delivered to the main-wash cycle of a Bosch dishwashing machine, at 55 C without prewash. The "all-in-one" compositions of examples 20 to 24 provide excellent removal of baked-on soils.
Example 20 21 22 23 24 Dishwashing detergent solvent composition KOH 4.60 5.65 2.10 1.47 1.05 H2SO4 3.94 3.94 MEA 4.00 4.00 8.00 STPP 22.00 22.00 22.00 22.00 SKTP 30.00 1,2-Propanediol 0.5 0.5 6.00 5.5 5.5 Boric acid 3.00 3.00 4.00 3.4 3.4 Polygel premix 1.18 1.18 1.18 1.18 1.18 SLF18 1.0 1.0 ACNI 3.0 2.1 2.1 C16 AO 0.40 0.308 0.308 CaC12 0.2 0.2 0.22 0.2 0.2 Na benzoate 0.20 0.20 0.20 0.20 0.20 Proxel GXL 0.01 0.01 0.05 0.01 0.01 FN3 0.60 0.60 0.90 0.76 0.76 Duramyl 0.27 Termamyl 0.17 0.26 0.23 0.23 Perfume 0.10 0.10 0.10 0.10 0.10 Dye 0.0024 0.0024 0.0024 0.0024 0.0024 Water to 100
Claims (43)
1. A method of removing cooked-, baked-, or burnt-on food soil from cookware and tableware comprising delivering a plurality of compositions including at least one organic solvent into the same or different cycles of an automatic dishwashing machine and washing the soiled cookware/tableware in the resulting solvent-containing wash liquor, wherein two of the plurality of compositions are delivered from a single storage means, separate storage means, or from separate zones of a multi-zone storage means, wherein the plurality of compositions is in the form of a multi-layer liquid or gel when delivered from the single storage means, and wherein the organic solvent composition comprises an organoamine solvent and glycol ether solvent in a weight ratio of from about 3:1 to about 1:3 and has a volatile organic content above 1 mm Hg of less than about 50%.
2. A method according to claim 1 wherein the plurality of compositions includes at least one organic solvent composition and at least one automatic dishwashing detergent composition, or wherein the plurality of compositions includes two or more solvent compositions.
3. A method according to claim 1 comprising delivering the organic solvent composition in the pre-wash cycle of the automatic dishwashing machine and thereafter delivering an automatic dishwashing detergent composition in the main-wash cycle of the automatic dishwashing machine.
4. A method according to claim 1 comprising delivering the organic solvent composition and a first automatic dishwashing detergent composition in the pre-wash cycle of the automatic dishwashing machine and thereafter delivering a second automatic dishwashing detergent composition in the main-wash cycle of the automatic dishwashing machine.
5. A method according to claim 1 comprising delivering the organic solvent composition and an automatic dishwashing detergent composition in the pre-wash and thereafter in the main-wash cycle of the automatic dishwashing machine.
6. A method according to claim 1 comprising delivering the organic solvent composition and an automatic dishwashing detergent composition in the main-wash cycle of the automatic dishwashing machine.
7. A method according to claim 1 comprising washing the cookware/tableware in the pre-wash cycle of the automatic dishwashing machine in the presence of the organic solvent composition and thereafter rinsing the cookware/tableware in the rinse cycle of the automatic dishwashing machine in the presence of an automatic dishwashing rinse composition.
8. A method according to claim 1 comprising delivering the organic solvent composition and an automatic dishwashing detergent composition from separate storage means into the same cycle of the automatic dishwashing machine.
9. A method according to claim 1 comprising delivering one or both of the organic solvent composition and an automatic dishwashing detergent composition contained in separate zones of a multi-zone storage means into the same or different cycles of the automatic dishwashing machine.
10. A method according to claim 9 comprising simultaneously delivering the organic solvent composition and automatic dishwashing detergent composition into the main wash cycle of the automatic dishwashing machine at a feed ratio of solvent composition to detergent composition in the range from about 5:1 to about 1:50.
11. A method according to claim 9 comprising sequentially delivering the organic solvent composition and automatic dishwashing detergent composition into the pre-wash and main-wash cycles respectively.
12. A method according to claim 9 wherein the multi-zone storage means is a multi-compartment container and wherein the physical form of the organic solvent composition and/or automatic dishwashing detergent compositions is such as to prevent intimate mixing of the compositions prior to contact thereof with the wash liquor.
13. A method according to claim 1 comprising delivering separate portions of a multi-phase detergent composition into the same or different cycles of the automatic dishwashing machine, wherein the multi-phase detergent composition comprises at least a first phase containing an organic solvent composition and at least a second phase containing an automatic dishwashing detergent composition.
14. A method according to claim 1 comprising delivering a plurality of the organic solvent compositions of different solvent characteristics into the same or different cycles of the automatic dishwashing machine.
15. A method according to claim 14 comprising delivering a first organic solvent composition and a first automatic dishwashing detergent composition in the pre-wash cycle and a second solvent composition and a second automatic dishwashing detergent composition in the main-wash cycle of the automatic dishwashing machine.
16. A method according to claim 1 wherein the wash liquor concentration of organic solvent is in the range from about 100 ppm to about 10,000 ppm.
17. A method according to claim 1 wherein the wash liquor concentration of organic solvent is in the range from about 500 ppm to about 5,000 ppm.
18. A method according to claim 1 wherein the wash liquor has a liquid surface tension of less than about 35 mN/m at 25°C and a pH of at least about 10.5.
19. A method according to claim 18 wherein the wash liquor has a liquid surface tension of less than about 30 mN/m at 25°C and a pH of at least about 10.5.
20. A method according to claim 19 wherein the wash liquor has a liquid surface tension of less than about 32 mN/m at 25°C and a pH of at least about 11.
21. A method according to claim 1 wherein the organic solvent composition is in a unit dose form adapted to provide controlled, delayed, sustained, triggered or slow release of organic solvent during one or more repeated washing cycles.
22. A method according to claim 1 wherein the organic solvent composition is in a unit dose form adapted to provide delayed release of organic solvent until after the pre-wash cycle of the dishwashing machine.
23. A method according to claim 1 wherein the organic solvent composition is in the form of a liquid, paste, cream or gel packaged in a single- or multi-compartment pouch, or absorbed onto a porous carrier material.
24. A method according to claim 1 wherein the organoamine solvent that removes the soil and has a liquid surface tension of less than about 24.5 mN/m at 25°C.
25. A method according to claim 24 wherein the organic solvent composition additionally comprises a spreading auxiliary selected from organic solvents, wetting agents and mixtures thereof.
26. A method according to claim 25 wherein the spreading auxiliary has a liquid surface tension of less than about 30 mN/m at 25°C.
27. A method according to claim 26 wherein the spreading auxiliary has a liquid surface tension of less than about 26 mN/m at 25°C.
28. A method according to claim 1 wherein the organic solvent composition has an advancing contact angle measured at 25°C on a polymerised grease-coated glass substrate of less than 20° and for mixed solvent systems has an advancing contact angle measured at 25°C that is less than the contact angle of any of the corresponding compositions containing the individual components of the solvent system.
29. A method according to claim 28 wherein the organic solvent composition has an advancing contact angle measured at 25°C on a polymerised grease-coated glass substrate of less than 10°, and for mixed solvent systems has an advancing contact angle measured at 25°C that is less than the advancing contact angle measured at 25°C
of any of the corresponding compositions containing the individual components of the solvent system.
of any of the corresponding compositions containing the individual components of the solvent system.
30. A method according to claim 1 wherein the organic solvent further comprises a solvent selected from the group consisting of alcohols, amines, esters, glycols, glycol ethers, terpenes and mixtures thereof.
31. A method according to claim 30 wherein the organic solvent is selected from organoamine solvents, alcoholic solvents, glycols and glycol derivatives and mixtures thereof.
32. A method according to claim 1 wherein the glycol ether solvent is selected from ethylene glycol monobutyl ether, diethylene glycol monobutyl ether, ethylene glycol monomethyl ether, ethylene glycol monoethyl ether, diethylene glycol monomethyl ether, diethylene glycol monomethyl ether, propylene glycol monobutyl ether, dipropylene glycol monobutyl ether, ethylene glycol phenyl ether and mixtures thereof.
33. A method of removing cooked-, baked-, or burnt-on food soil from cookware and tableware comprising delivering a plurality of compositions including at least one organic solvent composition into the same or different cycles of an automatic dishwashing machine and washing the soiled cookware/tableware in the resulting solvent-containing wash liquor, wherein the organic solvent comprises an organoamine solvent and glycol ether, in a weight ratio of from about 3:1 to about 1:3 and has a volatile organic content above 1 mm Hg of less than about 50%, and wherein the glycol ether is a mixture of diethylene glycol monobutyl ether and propylene glycol butyl ether in a weight ratio of from about 1:2 to about 2:1.
34. A method according to claim 1 wherein the organoamine solvent has a pKa of at least 8.8.
35. A method according to claim 34 wherein the organoamine solvent has a pKa of at least 9.8.
36. A method according to claim 1 wherein the organic solvent comprises a mixture of a first organoamine solvent having a pKa of 9.5 or less and a second organoamine solvent having a pKa greater than 9.5.
37. A method according to claim 1 wherein the organic solvent comprises one or more organoamines which is/are introduced into the wash liquor of the automatic dishwashing machine in the form of their ammonium salt at a wash liquor pH
above the highest pKa of the organoamine/s.
above the highest pKa of the organoamine/s.
38. A method according to claim 1 wherein the organic solvent is used in conjunction with a wetting agent that lowers the surface tension of the solvent, the wetting agent being selected from organic surfactants having a surface tension less than about 30 mN/m at 25°C.
39. A method according to claim 38 wherein the organic solvent is used in conjunction with a wetting agent that lowers the surface tension of the solvent, the wetting agent being selected from organic surfactants having a surface tension less than about 26 mN/m at 25°C.
40. A method according to claim 39 wherein the wetting agent is selected from silicone polyether copolymers.
41. A method according to claim 1 wherein the organic solvent is free of solvent components having a boiling point below about 150°C, flash point below about 100°C
or vapor pressure above about 1 mm Hg.
or vapor pressure above about 1 mm Hg.
42. A method according to claim 1 wherein the organic solvent system further comprises a solvent selected from:
(a) polar, hydrogen-bonding solvents having a Hansen solubility parameter of at least 20 (Mpa)1/2, a polarity parameter of at least 7 (Mpa)1/2 and a hydrogen bonding parameter of at least 10 (Mpa)1/2;
(b) polar non-hydrogen bonding solvents having a Hansen solubility parameter of at least 20 (Mpa)1/2, a polarity parameter of at least 7 (Mpa)1/2 and a hydrogen bonding parameter of less than 10 (Mpa)1/2, (c) amphiphilic solvents having a Hansen solubility parameter below 20 (Mpa)1/2, a polarity parameter of at least 7(Mpa)1/2 and a hydrogen bonding parameter of at least 10 (Mpa)1/2;
(d) non-polar solvents having a polarity parameter below 7 (Mpa)1/2 and a hydrogen bonding parameter below 10 (Mpa)1/2, and (e) mixtures thereof.
(a) polar, hydrogen-bonding solvents having a Hansen solubility parameter of at least 20 (Mpa)1/2, a polarity parameter of at least 7 (Mpa)1/2 and a hydrogen bonding parameter of at least 10 (Mpa)1/2;
(b) polar non-hydrogen bonding solvents having a Hansen solubility parameter of at least 20 (Mpa)1/2, a polarity parameter of at least 7 (Mpa)1/2 and a hydrogen bonding parameter of less than 10 (Mpa)1/2, (c) amphiphilic solvents having a Hansen solubility parameter below 20 (Mpa)1/2, a polarity parameter of at least 7(Mpa)1/2 and a hydrogen bonding parameter of at least 10 (Mpa)1/2;
(d) non-polar solvents having a polarity parameter below 7 (Mpa)1/2 and a hydrogen bonding parameter below 10 (Mpa)1/2, and (e) mixtures thereof.
43. A method of removing cooked-, baked-, or burnt-on food soil from cookware and tableware comprising delivering an organic solvent composition and a first automatic dishwashing detergent composition in the pre-wash cycle of an automatic dishwashing machine and thereafter delivering a second automatic dishwashing detergent composition in the main-wash cycle of the automatic dishwashing machine and washing the soiled cookware/tableware in the resulting solvent-containing wash liquor; wherein the organic solvent composition comprises organoamine solvent and glycol ether solvent, in a weight ratio of from about 3:1 to about 1:3;
wherein the organoamine solvent is selected from monoethanolamine, monoisopropanolamine, diethylethanolamine, ethyl diethanolamine, beta-aminealkanols, diethanolamine, disopropanolamine, 2-(methylamino)ethanol, triethanolamine, triispopropanolamine, and mixtures thereof; and wherein the glycol ether solvent is selected from ethylene glycol monobutyl ether, diethylene glycol, monobutyl ether, ethylene glycol monomethyl ether, ethylene glycol monoethyl ether, diethylene glycol monomethyl ether, diethylene glycol monoethyl ether, propylene glycol monobutyl ether, dipropylene glycol monobutyl ether, ethylene glycol phenyl ether, and mixtures thereof and wherein the organic solvent composition has a volatile organic content above 1 mm Hg of less than about 50%.
wherein the organoamine solvent is selected from monoethanolamine, monoisopropanolamine, diethylethanolamine, ethyl diethanolamine, beta-aminealkanols, diethanolamine, disopropanolamine, 2-(methylamino)ethanol, triethanolamine, triispopropanolamine, and mixtures thereof; and wherein the glycol ether solvent is selected from ethylene glycol monobutyl ether, diethylene glycol, monobutyl ether, ethylene glycol monomethyl ether, ethylene glycol monoethyl ether, diethylene glycol monomethyl ether, diethylene glycol monoethyl ether, propylene glycol monobutyl ether, dipropylene glycol monobutyl ether, ethylene glycol phenyl ether, and mixtures thereof and wherein the organic solvent composition has a volatile organic content above 1 mm Hg of less than about 50%.
Applications Claiming Priority (5)
Application Number | Priority Date | Filing Date | Title |
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PCT/US2000/019619 WO2002008370A2 (en) | 2000-07-19 | 2000-07-19 | Cleaning composition |
USPCT/US00/19619 | 2000-07-19 | ||
PCT/US2000/020255 WO2002008371A2 (en) | 2000-02-17 | 2000-07-25 | Cleaning composition |
USPCT/US00/20255 | 2000-07-25 | ||
PCT/US2000/034909 WO2002008376A1 (en) | 2000-07-19 | 2000-12-21 | Cleaning composition |
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CA2414140C true CA2414140C (en) | 2008-06-03 |
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CA002416327A Expired - Fee Related CA2416327C (en) | 2000-07-19 | 2000-12-21 | Low surface tension, alkaline hard surface cleaner containing an organoamine |
CA002414140A Expired - Lifetime CA2414140C (en) | 2000-07-19 | 2000-12-21 | Automatic dishwashing method employing an organic solvent system |
CA002416326A Abandoned CA2416326A1 (en) | 2000-07-19 | 2000-12-21 | Low surface tension, alkaline hard surface cleaner comprising a soil welling agent and a spreading auxiliary |
CA002414133A Expired - Fee Related CA2414133C (en) | 2000-07-19 | 2000-12-21 | Automatic dishwashing method employing an organic solvent system |
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CA002416327A Expired - Fee Related CA2416327C (en) | 2000-07-19 | 2000-12-21 | Low surface tension, alkaline hard surface cleaner containing an organoamine |
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CA002416326A Abandoned CA2416326A1 (en) | 2000-07-19 | 2000-12-21 | Low surface tension, alkaline hard surface cleaner comprising a soil welling agent and a spreading auxiliary |
CA002414133A Expired - Fee Related CA2414133C (en) | 2000-07-19 | 2000-12-21 | Automatic dishwashing method employing an organic solvent system |
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Families Citing this family (46)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US6683036B2 (en) | 2000-07-19 | 2004-01-27 | The Procter & Gamble Company | Cleaning composition |
US6557732B2 (en) | 2000-07-19 | 2003-05-06 | The Procter & Gamble Company | Detergent pack |
US7125828B2 (en) | 2000-11-27 | 2006-10-24 | The Procter & Gamble Company | Detergent products, methods and manufacture |
US8658585B2 (en) | 2000-11-27 | 2014-02-25 | Tanguy Marie Louise Alexandre Catlin | Detergent products, methods and manufacture |
US6492312B1 (en) * | 2001-03-16 | 2002-12-10 | Unilever Home & Personal Care Usa, Division Of Conopco, Inc. | Water soluble sachet with a dishwashing enhancing particle |
EP1245668A3 (en) * | 2001-03-30 | 2003-09-17 | The Procter & Gamble Company | Cleaning composition |
US7008911B2 (en) | 2002-09-06 | 2006-03-07 | Ecolab, Inc. | Non-surfactant solubilizing agent |
US6767881B1 (en) | 2003-03-19 | 2004-07-27 | Ecolab, Inc. | Cleaning concentrate |
EP1518922A1 (en) * | 2003-09-26 | 2005-03-30 | Unilever N.V. | Machine dishwashing formulations |
DE102004055077A1 (en) * | 2004-10-22 | 2006-07-06 | Henkel Kgaa | Detergent or detergent dosing unit 2 |
JP2008531829A (en) * | 2005-03-04 | 2008-08-14 | ザ プロクター アンド ギャンブル カンパニー | Automatic dishwashing composition having a corrosion inhibitor |
ES2346979T3 (en) * | 2005-03-07 | 2010-10-22 | THE PROCTER & GAMBLE COMPANY | DETERGENT OR WHITENING COMPOSITIONS. |
US7147634B2 (en) | 2005-05-12 | 2006-12-12 | Orion Industries, Ltd. | Electrosurgical electrode and method of manufacturing same |
US8814861B2 (en) | 2005-05-12 | 2014-08-26 | Innovatech, Llc | Electrosurgical electrode and method of manufacturing same |
US7099143B1 (en) | 2005-05-24 | 2006-08-29 | Avx Corporation | Wet electrolytic capacitors |
WO2007013636A1 (en) * | 2005-07-25 | 2007-02-01 | Tokuyama Corporation | Cleaning agent |
JP4832825B2 (en) * | 2005-07-25 | 2011-12-07 | 株式会社トクヤマ | Manufacturing method of plastic lens |
US20100234263A1 (en) * | 2006-03-21 | 2010-09-16 | The Procter & Gamble Company | Nano-fluids as cleaning compositions for cleaning soiled surfaces, a method for formulation and use |
EP1837394A1 (en) * | 2006-03-21 | 2007-09-26 | The Procter and Gamble Company | Cleaning Method |
CA2675259A1 (en) * | 2007-02-09 | 2008-08-21 | The Procter & Gamble Company | Perfume systems |
DE102007019458A1 (en) * | 2007-04-25 | 2008-10-30 | Basf Se | Phosphate-free machine dishwashing detergent with excellent rinse performance |
DE102007019457A1 (en) * | 2007-04-25 | 2008-10-30 | Basf Se | Machine dishwashing detergent with excellent rinse performance |
GB0711992D0 (en) | 2007-06-21 | 2007-08-01 | Reckitt Benckiser Inc | Alkaline hard surface cleaning composition |
US20090197790A1 (en) * | 2008-02-05 | 2009-08-06 | Amcol International Corporation | Drip resistant cleaning compositions |
US20090258810A1 (en) * | 2008-04-01 | 2009-10-15 | Brian Xiaoqing Song | Gel automatic dishwashing detergent composition |
KR101482110B1 (en) * | 2008-05-23 | 2015-01-13 | 엘지전자 주식회사 | Washing machine |
DE102009000879A1 (en) * | 2009-02-16 | 2010-08-19 | Henkel Ag & Co. Kgaa | cleaning supplies |
EP2443221A4 (en) | 2009-06-15 | 2012-11-21 | Ecolab Usa Inc | High alkaline cleaners, cleaning systems and methods of use for cleaning zero trans fat soils |
EP2443222B1 (en) * | 2009-06-15 | 2018-03-14 | Ecolab USA Inc. | Methods of use for cleaning zero trans fat soils |
US9512387B2 (en) | 2011-02-11 | 2016-12-06 | Dubois Chemicals, Inc. | Cleaning compositions for removing polymeric contaminants from papermaking surfaces |
US8616375B2 (en) | 2012-01-13 | 2013-12-31 | Whirlpool Corporation | Packets for treating chemistry |
EP2746376B1 (en) * | 2012-12-21 | 2017-08-30 | The Procter & Gamble Company | Dishwashing composition |
EP3116985B1 (en) | 2014-03-12 | 2018-07-25 | The Procter and Gamble Company | Detergent composition |
EP2940116B1 (en) * | 2014-04-30 | 2018-10-17 | The Procter and Gamble Company | Detergent |
US9856398B2 (en) | 2014-12-22 | 2018-01-02 | Dubois Chemicals, Inc. | Method for controlling deposits on papermaking surfaces |
EP3118293B1 (en) | 2015-07-13 | 2020-09-09 | The Procter and Gamble Company | Cleaning product |
PL3118299T3 (en) | 2015-07-13 | 2019-04-30 | Procter & Gamble | Cleaning product |
EP3118294B1 (en) | 2015-07-13 | 2018-10-17 | The Procter and Gamble Company | Cleaning product |
PL3118301T3 (en) | 2015-07-13 | 2019-04-30 | Procter & Gamble | Cleaning product |
US10851330B2 (en) | 2015-07-29 | 2020-12-01 | Dubois Chemicals, Inc. | Method of improving paper machine fabric performance |
WO2018145220A1 (en) * | 2017-02-13 | 2018-08-16 | Fenoglio Jose Luis | Granular alkaline cleaner, descaler and disinfectant for applying in a single step, compositions and method for applying to hard surfaces and clean-in-place systems |
CA3139842A1 (en) * | 2019-05-10 | 2020-11-19 | The Procter & Gamble Company | Hard surface cleaning compositions comprising alkoxylated phenols and perfumes and cleaning pads and methods for using such cleaning compositions |
EP4053254A1 (en) | 2021-03-04 | 2022-09-07 | The Procter & Gamble Company | Hard surface cleaning composition comprising polyalkylene glycol |
EP4098121A1 (en) | 2021-06-04 | 2022-12-07 | The Procter & Gamble Company | Antimicrobial composition |
WO2022256369A1 (en) | 2021-06-04 | 2022-12-08 | The Procter & Gamble Company | Antimicrobial composition |
EP4368692A1 (en) | 2022-11-10 | 2024-05-15 | The Procter & Gamble Company | Method to provide malodor removal and/or malodor prevention |
Family Cites Families (35)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
DE1912364A1 (en) * | 1969-03-12 | 1970-11-05 | Bosch Hausgeraete Gmbh | Dishwasher |
DE1945038A1 (en) * | 1969-09-05 | 1971-03-11 | Miele & Cie | Dishwasher agent |
US3645421A (en) * | 1970-02-16 | 1972-02-29 | American Dish Service | Method of adding ingredients to a dishwashing medium |
US4218264A (en) * | 1979-03-09 | 1980-08-19 | Federighi George B | Dishwasher utilizing pump impeller suction for feeding detergent, sanitizing agent and rinse aid in timed sequences |
JPS59136399A (en) * | 1983-01-26 | 1984-08-04 | 花王株式会社 | Liquid detergent composition |
US4606775A (en) * | 1984-04-05 | 1986-08-19 | Purex Corporation | Automatic dishwasher in a dual functioning system |
US4964185A (en) * | 1986-01-09 | 1990-10-23 | Ecolab Inc. | Chemical solution dispenser apparatus and method of using |
IT1200285B (en) * | 1986-08-12 | 1989-01-12 | Mira Lanza Spa | NON-Aqueous LIQUID DETERGENT AND PROCEDURE FOR ITS MANUFACTURE |
GB2200365A (en) * | 1987-01-26 | 1988-08-03 | Goodjet Ltd | Detergent composition |
US5102573A (en) * | 1987-04-10 | 1992-04-07 | Colgate Palmolive Co. | Detergent composition |
US4921129A (en) * | 1988-07-11 | 1990-05-01 | Pacific Biosystems, Inc. | Liquid dispensing module |
EP0429124A1 (en) * | 1989-11-21 | 1991-05-29 | The Procter & Gamble Company | Chlorine-free liquid automatic dishwashing compositions |
AU637902B2 (en) * | 1990-05-07 | 1993-06-10 | Colgate-Palmolive Company, The | Nonaqueous liquid automatic dishwasher detergent composition |
AU655274B2 (en) * | 1991-05-31 | 1994-12-15 | Colgate-Palmolive Company, The | Nonaqueous liquid, phosphate-free, improved automatic dishwashing composition containing enzymes |
US5527483A (en) * | 1991-05-31 | 1996-06-18 | Colgate Palmolive Co. | Nonaqueous gelled automatic dishwashing composition containing enzymes |
US5267676A (en) * | 1992-04-06 | 1993-12-07 | Lord Anita C | Liquid dispenser for use with washing machine |
EP0690909B1 (en) * | 1993-03-30 | 1997-10-08 | Minnesota Mining And Manufacturing Company | Cleaning compositions and methods of use |
US5576281A (en) * | 1993-04-05 | 1996-11-19 | Olin Corporation | Biogradable low foaming surfactants as a rinse aid for autodish applications |
US5750487A (en) * | 1993-04-12 | 1998-05-12 | Colgate-Palmolive Co. | Tricritical point compositions |
DE69425142T2 (en) * | 1993-06-01 | 2001-03-22 | Ecolab Inc., St. Paul | THICKENED CLEANER FOR HARD SURFACES |
WO1995006102A1 (en) * | 1993-08-27 | 1995-03-02 | Colgate-Palmolive Company | Nonaqueous liquid microemulsion compositions |
JPH08170099A (en) * | 1994-12-20 | 1996-07-02 | Johnson Kk | Washing of fat and oil dirt and detergent |
AR003210A1 (en) * | 1995-08-07 | 1998-07-08 | Procter & Gamble | DETERGENT COMPOSITIONS FOR CLOTHING WASHING INCLUDING A DETERSIVE SURFACTANT OF AMINE AND SPECIALLY SELECTED PERFUMES. |
GB9521719D0 (en) * | 1995-10-24 | 1996-01-03 | Gw Chemicals Ltd | Cleaning apparatus |
US5929007A (en) * | 1996-05-24 | 1999-07-27 | Reckitt & Colman Inc. | Alkaline aqueous hard surface cleaning compositions |
CA2219653C (en) * | 1996-10-29 | 2001-12-25 | The Procter & Gamble Company | Non-foaming liquid hard surface detergent compositions |
US5919312A (en) * | 1997-03-18 | 1999-07-06 | The Procter & Gamble Company | Compositions and methods for removing oily or greasy soils |
US5919440A (en) * | 1997-05-05 | 1999-07-06 | Procter & Gamble Company | Personal care compositions containing an odor masking base |
WO1998056337A1 (en) * | 1997-06-09 | 1998-12-17 | The Procter & Gamble Company | Malodor reducing composition containing amber and musk materials |
ID28183A (en) * | 1997-06-09 | 2001-05-10 | Procter & Gamble | FOOD CLEANING COMPOSITION CONTAINING CYCODODSTRINE |
CA2220312C (en) * | 1997-11-10 | 1999-11-09 | Murugesu Nandhakumaran | Radio receiver and rebroadcaster |
JPH11302693A (en) * | 1998-04-16 | 1999-11-02 | Minnesota Mining & Mfg Co <3M> | Concentrated detergent composition |
JP2992277B1 (en) * | 1998-09-22 | 1999-12-20 | 花王株式会社 | Aqueous liquid cleaner |
GB2346319B (en) * | 1999-02-05 | 2002-12-04 | Unilever Plc | A machine dishwashing kit |
DE20001957U1 (en) * | 2000-02-04 | 2000-03-30 | Unilever N.V., Rotterdam | Material set for washing dishes by machine |
-
2000
- 2000-07-19 WO PCT/US2000/019619 patent/WO2002008370A2/en active Application Filing
- 2000-12-21 ES ES00986682T patent/ES2352670T3/en not_active Expired - Lifetime
- 2000-12-21 CA CA002416327A patent/CA2416327C/en not_active Expired - Fee Related
- 2000-12-21 WO PCT/US2000/034908 patent/WO2002008375A1/en active IP Right Grant
- 2000-12-21 WO PCT/US2000/034906 patent/WO2002008374A1/en active Application Filing
- 2000-12-21 ES ES00986683T patent/ES2339420T3/en not_active Expired - Lifetime
- 2000-12-21 MX MXPA03000490A patent/MXPA03000490A/en unknown
- 2000-12-21 AU AU2001224494A patent/AU2001224494A1/en not_active Abandoned
- 2000-12-21 ES ES00988267T patent/ES2306676T3/en not_active Expired - Lifetime
- 2000-12-21 AT AT00988267T patent/ATE395405T1/en not_active IP Right Cessation
- 2000-12-21 CA CA002414140A patent/CA2414140C/en not_active Expired - Lifetime
- 2000-12-21 MX MXPA03000491A patent/MXPA03000491A/en active IP Right Grant
- 2000-12-21 AT AT00986682T patent/ATE481471T1/en not_active IP Right Cessation
- 2000-12-21 MX MXPA03000492A patent/MXPA03000492A/en active IP Right Grant
- 2000-12-21 WO PCT/US2000/034910 patent/WO2002008509A1/en active Application Filing
- 2000-12-21 MX MXPA03000493A patent/MXPA03000493A/en active IP Right Grant
- 2000-12-21 EP EP00988267A patent/EP1305390B1/en not_active Expired - Lifetime
- 2000-12-21 JP JP2002514259A patent/JP2004515569A/en active Pending
- 2000-12-21 CA CA002416326A patent/CA2416326A1/en not_active Abandoned
- 2000-12-21 EP EP00986682A patent/EP1305388B1/en not_active Expired - Lifetime
- 2000-12-21 AU AU2001222875A patent/AU2001222875A1/en not_active Abandoned
- 2000-12-21 AT AT00986684T patent/ATE342336T1/en not_active IP Right Cessation
- 2000-12-21 WO PCT/US2000/034909 patent/WO2002008376A1/en active Application Filing
- 2000-12-21 WO PCT/US2000/034907 patent/WO2002008373A1/en active Application Filing
- 2000-12-21 JP JP2002514258A patent/JP3962327B2/en not_active Expired - Fee Related
- 2000-12-21 AU AU2001222874A patent/AU2001222874A1/en not_active Abandoned
- 2000-12-21 JP JP2002513861A patent/JP2004509175A/en active Pending
- 2000-12-21 EP EP00986684A patent/EP1305389B1/en not_active Revoked
- 2000-12-21 AU AU2001222876A patent/AU2001222876A1/en not_active Abandoned
- 2000-12-21 CA CA002414133A patent/CA2414133C/en not_active Expired - Fee Related
- 2000-12-21 ES ES00986684T patent/ES2273742T3/en not_active Expired - Lifetime
- 2000-12-21 AU AU2001222873A patent/AU2001222873A1/en not_active Abandoned
- 2000-12-21 JP JP2002514260A patent/JP2004509176A/en active Pending
- 2000-12-21 EP EP00986683A patent/EP1305383B1/en not_active Expired - Lifetime
- 2000-12-21 AT AT00986683T patent/ATE455836T1/en not_active IP Right Cessation
- 2000-12-21 DE DE60031309T patent/DE60031309T2/en not_active Revoked
-
2001
- 2001-07-18 ES ES01959010T patent/ES2225589T3/en not_active Expired - Lifetime
- 2001-07-18 EP EP04023010A patent/EP1493803B1/en not_active Expired - Lifetime
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