CA2069853A1 - Phosphate-containing powder automatic dishwashing composition with enzymes - Google Patents
Phosphate-containing powder automatic dishwashing composition with enzymesInfo
- Publication number
- CA2069853A1 CA2069853A1 CA002069853A CA2069853A CA2069853A1 CA 2069853 A1 CA2069853 A1 CA 2069853A1 CA 002069853 A CA002069853 A CA 002069853A CA 2069853 A CA2069853 A CA 2069853A CA 2069853 A1 CA2069853 A1 CA 2069853A1
- Authority
- CA
- Canada
- Prior art keywords
- enzyme
- dishwashing composition
- weight
- percent
- composition according
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Abandoned
Links
- 239000000203 mixture Substances 0.000 title claims abstract description 119
- 102000004190 Enzymes Human genes 0.000 title claims abstract description 57
- 108090000790 Enzymes Proteins 0.000 title claims abstract description 56
- 238000004851 dishwashing Methods 0.000 title claims abstract description 51
- 239000000843 powder Substances 0.000 title description 46
- 229910019142 PO4 Inorganic materials 0.000 title description 12
- NBIIXXVUZAFLBC-UHFFFAOYSA-K phosphate Chemical compound [O-]P([O-])([O-])=O NBIIXXVUZAFLBC-UHFFFAOYSA-K 0.000 title description 11
- 239000010452 phosphate Substances 0.000 title description 11
- 108091005804 Peptidases Proteins 0.000 claims abstract description 24
- 239000007844 bleaching agent Substances 0.000 claims abstract description 22
- 239000002736 nonionic surfactant Substances 0.000 claims abstract description 22
- 150000003839 salts Chemical class 0.000 claims abstract description 19
- 229910052910 alkali metal silicate Inorganic materials 0.000 claims abstract description 7
- 102100037486 Reverse transcriptase/ribonuclease H Human genes 0.000 claims abstract 7
- 239000003599 detergent Substances 0.000 claims description 87
- 102000035195 Peptidases Human genes 0.000 claims description 17
- 102000013142 Amylases Human genes 0.000 claims description 14
- 108010065511 Amylases Proteins 0.000 claims description 14
- 239000007788 liquid Substances 0.000 claims description 10
- 102000004882 Lipase Human genes 0.000 claims description 9
- 108090001060 Lipase Proteins 0.000 claims description 9
- 229920002125 Sokalan® Polymers 0.000 claims description 9
- 102000005158 Subtilisins Human genes 0.000 claims description 9
- 108010056079 Subtilisins Proteins 0.000 claims description 9
- 239000002518 antifoaming agent Substances 0.000 claims description 9
- 229920000058 polyacrylate Polymers 0.000 claims description 9
- 239000012190 activator Substances 0.000 claims description 8
- 229910052783 alkali metal Inorganic materials 0.000 claims description 8
- 239000003795 chemical substances by application Substances 0.000 claims description 8
- 150000001340 alkali metals Chemical class 0.000 claims description 5
- 229920001577 copolymer Polymers 0.000 claims description 4
- 239000003605 opacifier Substances 0.000 claims description 4
- 239000002304 perfume Substances 0.000 claims description 4
- QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical compound [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 claims description 3
- 238000005260 corrosion Methods 0.000 claims description 3
- 239000001301 oxygen Substances 0.000 claims description 3
- 229910052760 oxygen Inorganic materials 0.000 claims description 3
- 229920000642 polymer Polymers 0.000 claims description 3
- 239000004584 polyacrylic acid Substances 0.000 claims description 2
- 239000002671 adjuvant Substances 0.000 claims 1
- 239000003352 sequestering agent Substances 0.000 claims 1
- 238000004140 cleaning Methods 0.000 abstract description 18
- 229940088598 enzyme Drugs 0.000 description 57
- 239000000047 product Substances 0.000 description 44
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 33
- -1 polyoxyethylene chain Polymers 0.000 description 29
- CDBYLPFSWZWCQE-UHFFFAOYSA-L Sodium Carbonate Chemical compound [Na+].[Na+].[O-]C([O-])=O CDBYLPFSWZWCQE-UHFFFAOYSA-L 0.000 description 22
- 239000000460 chlorine Substances 0.000 description 22
- 230000000694 effects Effects 0.000 description 22
- 235000013601 eggs Nutrition 0.000 description 20
- 239000002689 soil Substances 0.000 description 20
- ZAMOUSCENKQFHK-UHFFFAOYSA-N Chlorine atom Chemical compound [Cl] ZAMOUSCENKQFHK-UHFFFAOYSA-N 0.000 description 17
- 125000000217 alkyl group Chemical group 0.000 description 17
- 229910052801 chlorine Inorganic materials 0.000 description 17
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 description 16
- 239000004094 surface-active agent Substances 0.000 description 15
- 229920001282 polysaccharide Polymers 0.000 description 14
- 239000005017 polysaccharide Substances 0.000 description 14
- IAYPIBMASNFSPL-UHFFFAOYSA-N Ethylene oxide Chemical compound C1CO1 IAYPIBMASNFSPL-UHFFFAOYSA-N 0.000 description 13
- 125000004432 carbon atom Chemical group C* 0.000 description 13
- NTHWMYGWWRZVTN-UHFFFAOYSA-N sodium silicate Chemical compound [Na+].[Na+].[O-][Si]([O-])=O NTHWMYGWWRZVTN-UHFFFAOYSA-N 0.000 description 13
- 150000001875 compounds Chemical class 0.000 description 12
- 239000010408 film Substances 0.000 description 12
- 239000000126 substance Substances 0.000 description 12
- 150000002191 fatty alcohols Chemical class 0.000 description 11
- 238000000034 method Methods 0.000 description 11
- 235000021317 phosphate Nutrition 0.000 description 11
- 239000004115 Sodium Silicate Substances 0.000 description 10
- 229910000029 sodium carbonate Inorganic materials 0.000 description 10
- 235000017550 sodium carbonate Nutrition 0.000 description 10
- 229910052911 sodium silicate Inorganic materials 0.000 description 10
- 235000019832 sodium triphosphate Nutrition 0.000 description 10
- 238000005187 foaming Methods 0.000 description 9
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 8
- 238000009472 formulation Methods 0.000 description 8
- 239000000463 material Substances 0.000 description 8
- 239000000377 silicon dioxide Substances 0.000 description 8
- DGAQECJNVWCQMB-PUAWFVPOSA-M Ilexoside XXIX Chemical compound C[C@@H]1CC[C@@]2(CC[C@@]3(C(=CC[C@H]4[C@]3(CC[C@@H]5[C@@]4(CC[C@@H](C5(C)C)OS(=O)(=O)[O-])C)C)[C@@H]2[C@]1(C)O)C)C(=O)O[C@H]6[C@@H]([C@H]([C@@H]([C@H](O6)CO)O)O)O.[Na+] DGAQECJNVWCQMB-PUAWFVPOSA-M 0.000 description 7
- 230000003625 amylolytic effect Effects 0.000 description 7
- 239000004615 ingredient Substances 0.000 description 7
- 229910052708 sodium Inorganic materials 0.000 description 7
- 239000011734 sodium Substances 0.000 description 7
- AYEKOFBPNLCAJY-UHFFFAOYSA-O thiamine pyrophosphate Chemical compound CC1=C(CCOP(O)(=O)OP(O)(O)=O)SC=[N+]1CC1=CN=C(C)N=C1N AYEKOFBPNLCAJY-UHFFFAOYSA-O 0.000 description 7
- 102000002322 Egg Proteins Human genes 0.000 description 6
- 108010000912 Egg Proteins Proteins 0.000 description 6
- GOOHAUXETOMSMM-UHFFFAOYSA-N Propylene oxide Chemical compound CC1CO1 GOOHAUXETOMSMM-UHFFFAOYSA-N 0.000 description 6
- 150000001720 carbohydrates Chemical group 0.000 description 6
- 229910052681 coesite Inorganic materials 0.000 description 6
- 229910052906 cristobalite Inorganic materials 0.000 description 6
- 235000013345 egg yolk Nutrition 0.000 description 6
- 210000002969 egg yolk Anatomy 0.000 description 6
- 229930182478 glucoside Natural products 0.000 description 6
- 102000004169 proteins and genes Human genes 0.000 description 6
- 108090000623 proteins and genes Proteins 0.000 description 6
- 235000012239 silicon dioxide Nutrition 0.000 description 6
- 229910052682 stishovite Inorganic materials 0.000 description 6
- 239000008399 tap water Substances 0.000 description 6
- 235000020679 tap water Nutrition 0.000 description 6
- 229910052905 tridymite Inorganic materials 0.000 description 6
- UXVMQQNJUSDDNG-UHFFFAOYSA-L Calcium chloride Chemical compound [Cl-].[Cl-].[Ca+2] UXVMQQNJUSDDNG-UHFFFAOYSA-L 0.000 description 5
- WQZGKKKJIJFFOK-GASJEMHNSA-N Glucose Natural products OC[C@H]1OC(O)[C@H](O)[C@@H](O)[C@@H]1O WQZGKKKJIJFFOK-GASJEMHNSA-N 0.000 description 5
- KKCBUQHMOMHUOY-UHFFFAOYSA-N Na2O Inorganic materials [O-2].[Na+].[Na+] KKCBUQHMOMHUOY-UHFFFAOYSA-N 0.000 description 5
- PMZURENOXWZQFD-UHFFFAOYSA-L Sodium Sulfate Chemical compound [Na+].[Na+].[O-]S([O-])(=O)=O PMZURENOXWZQFD-UHFFFAOYSA-L 0.000 description 5
- 229920002472 Starch Polymers 0.000 description 5
- 125000003545 alkoxy group Chemical group 0.000 description 5
- 239000008103 glucose Substances 0.000 description 5
- 150000008131 glucosides Chemical class 0.000 description 5
- 125000001165 hydrophobic group Chemical group 0.000 description 5
- 229910052938 sodium sulfate Inorganic materials 0.000 description 5
- 235000011152 sodium sulphate Nutrition 0.000 description 5
- 239000000243 solution Substances 0.000 description 5
- 235000019698 starch Nutrition 0.000 description 5
- 238000003860 storage Methods 0.000 description 5
- 230000015556 catabolic process Effects 0.000 description 4
- 238000006731 degradation reaction Methods 0.000 description 4
- 150000008195 galaktosides Chemical class 0.000 description 4
- 230000002209 hydrophobic effect Effects 0.000 description 4
- 238000002156 mixing Methods 0.000 description 4
- 229920001296 polysiloxane Polymers 0.000 description 4
- 239000010457 zeolite Substances 0.000 description 4
- RZVAJINKPMORJF-UHFFFAOYSA-N Acetaminophen Chemical compound CC(=O)NC1=CC=C(O)C=C1 RZVAJINKPMORJF-UHFFFAOYSA-N 0.000 description 3
- 241000193830 Bacillus <bacterium> Species 0.000 description 3
- 229910000323 aluminium silicate Inorganic materials 0.000 description 3
- 239000001110 calcium chloride Substances 0.000 description 3
- 229910001628 calcium chloride Inorganic materials 0.000 description 3
- 235000011148 calcium chloride Nutrition 0.000 description 3
- 229930182479 fructoside Natural products 0.000 description 3
- 125000002519 galactosyl group Chemical group C1([C@H](O)[C@@H](O)[C@@H](O)[C@H](O1)CO)* 0.000 description 3
- 239000011521 glass Substances 0.000 description 3
- 125000002791 glucosyl group Chemical group C1([C@H](O)[C@@H](O)[C@H](O)[C@H](O1)CO)* 0.000 description 3
- 238000010348 incorporation Methods 0.000 description 3
- 230000002366 lipolytic effect Effects 0.000 description 3
- 239000002245 particle Substances 0.000 description 3
- 229940024999 proteolytic enzymes for treatment of wounds and ulcers Drugs 0.000 description 3
- 235000019795 sodium metasilicate Nutrition 0.000 description 3
- 239000007921 spray Substances 0.000 description 3
- 239000000375 suspending agent Substances 0.000 description 3
- 238000010998 test method Methods 0.000 description 3
- SMZOUWXMTYCWNB-UHFFFAOYSA-N 2-(2-methoxy-5-methylphenyl)ethanamine Chemical compound COC1=CC=C(C)C=C1CCN SMZOUWXMTYCWNB-UHFFFAOYSA-N 0.000 description 2
- NIXOWILDQLNWCW-UHFFFAOYSA-N 2-Propenoic acid Natural products OC(=O)C=C NIXOWILDQLNWCW-UHFFFAOYSA-N 0.000 description 2
- IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 description 2
- 244000075850 Avena orientalis Species 0.000 description 2
- 235000007319 Avena orientalis Nutrition 0.000 description 2
- BVKZGUZCCUSVTD-UHFFFAOYSA-L Carbonate Chemical compound [O-]C([O-])=O BVKZGUZCCUSVTD-UHFFFAOYSA-L 0.000 description 2
- 229920000388 Polyphosphate Polymers 0.000 description 2
- BGRWYDHXPHLNKA-UHFFFAOYSA-N Tetraacetylethylenediamine Chemical compound CC(=O)N(C(C)=O)CCN(C(C)=O)C(C)=O BGRWYDHXPHLNKA-UHFFFAOYSA-N 0.000 description 2
- GWEVSGVZZGPLCZ-UHFFFAOYSA-N Titan oxide Chemical group O=[Ti]=O GWEVSGVZZGPLCZ-UHFFFAOYSA-N 0.000 description 2
- 241001625808 Trona Species 0.000 description 2
- 238000010521 absorption reaction Methods 0.000 description 2
- 239000003377 acid catalyst Substances 0.000 description 2
- 229910000272 alkali metal oxide Inorganic materials 0.000 description 2
- 150000004703 alkoxides Chemical group 0.000 description 2
- 239000002585 base Substances 0.000 description 2
- 239000011324 bead Substances 0.000 description 2
- 238000009835 boiling Methods 0.000 description 2
- 239000007859 condensation product Substances 0.000 description 2
- 230000002255 enzymatic effect Effects 0.000 description 2
- 239000006260 foam Substances 0.000 description 2
- 150000008132 fructosides Chemical class 0.000 description 2
- 150000004676 glycans Chemical class 0.000 description 2
- 229930182470 glycoside Natural products 0.000 description 2
- 239000004519 grease Substances 0.000 description 2
- PMYUVOOOQDGQNW-UHFFFAOYSA-N hexasodium;trioxido(trioxidosilyloxy)silane Chemical compound [Na+].[Na+].[Na+].[Na+].[Na+].[Na+].[O-][Si]([O-])([O-])O[Si]([O-])([O-])[O-] PMYUVOOOQDGQNW-UHFFFAOYSA-N 0.000 description 2
- 238000011086 high cleaning Methods 0.000 description 2
- 125000002887 hydroxy group Chemical group [H]O* 0.000 description 2
- 230000000977 initiatory effect Effects 0.000 description 2
- 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 2
- 238000011056 performance test Methods 0.000 description 2
- 150000003013 phosphoric acid derivatives Chemical class 0.000 description 2
- 229920001983 poloxamer Polymers 0.000 description 2
- 229920000141 poly(maleic anhydride) Polymers 0.000 description 2
- 239000001205 polyphosphate Substances 0.000 description 2
- 235000011176 polyphosphates Nutrition 0.000 description 2
- 235000021395 porridge Nutrition 0.000 description 2
- BWHMMNNQKKPAPP-UHFFFAOYSA-L potassium carbonate Chemical compound [K+].[K+].[O-]C([O-])=O BWHMMNNQKKPAPP-UHFFFAOYSA-L 0.000 description 2
- 238000002360 preparation method Methods 0.000 description 2
- 238000012545 processing Methods 0.000 description 2
- 150000004760 silicates Chemical class 0.000 description 2
- 239000001509 sodium citrate Substances 0.000 description 2
- NLJMYIDDQXHKNR-UHFFFAOYSA-K sodium citrate Chemical compound O.O.[Na+].[Na+].[Na+].[O-]C(=O)CC(O)(CC([O-])=O)C([O-])=O NLJMYIDDQXHKNR-UHFFFAOYSA-K 0.000 description 2
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- GLVYLTSKTCWWJR-UHFFFAOYSA-N 2-carbonoperoxoylbenzoic acid Chemical compound OOC(=O)C1=CC=CC=C1C(O)=O GLVYLTSKTCWWJR-UHFFFAOYSA-N 0.000 description 1
- XSVSPKKXQGNHMD-UHFFFAOYSA-N 5-bromo-3-methyl-1,2-thiazole Chemical compound CC=1C=C(Br)SN=1 XSVSPKKXQGNHMD-UHFFFAOYSA-N 0.000 description 1
- BOJWYAVUTOTZOO-UHFFFAOYSA-N 6-ethylidenecyclohexa-2,4-diene-1-carboxylic acid Chemical compound CC=C1C=CC=CC1C(O)=O BOJWYAVUTOTZOO-UHFFFAOYSA-N 0.000 description 1
- 238000012935 Averaging Methods 0.000 description 1
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- 125000001421 myristyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 description 1
- 229910052757 nitrogen Inorganic materials 0.000 description 1
- 125000000913 palmityl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 description 1
- 210000000496 pancreas Anatomy 0.000 description 1
- 229940055729 papain Drugs 0.000 description 1
- 235000019834 papain Nutrition 0.000 description 1
- 235000011837 pasties Nutrition 0.000 description 1
- 125000002958 pentadecyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 description 1
- HJKYXKSLRZKNSI-UHFFFAOYSA-I pentapotassium;hydrogen sulfate;oxido sulfate;sulfuric acid Chemical compound [K+].[K+].[K+].[K+].[K+].OS([O-])(=O)=O.[O-]S([O-])(=O)=O.OS(=O)(=O)O[O-].OS(=O)(=O)O[O-] HJKYXKSLRZKNSI-UHFFFAOYSA-I 0.000 description 1
- 229940111202 pepsin Drugs 0.000 description 1
- 150000004965 peroxy acids Chemical class 0.000 description 1
- 125000005342 perphosphate group Chemical group 0.000 description 1
- 229920000435 poly(dimethylsiloxane) Polymers 0.000 description 1
- 229920001223 polyethylene glycol Polymers 0.000 description 1
- 238000006116 polymerization reaction Methods 0.000 description 1
- 229920006324 polyoxymethylene Polymers 0.000 description 1
- 150000004804 polysaccharides Polymers 0.000 description 1
- 229910000028 potassium bicarbonate Inorganic materials 0.000 description 1
- 235000015497 potassium bicarbonate Nutrition 0.000 description 1
- 239000011736 potassium bicarbonate Substances 0.000 description 1
- 229910000027 potassium carbonate Inorganic materials 0.000 description 1
- 235000011181 potassium carbonates Nutrition 0.000 description 1
- TYJJADVDDVDEDZ-UHFFFAOYSA-M potassium hydrogencarbonate Chemical compound [K+].OC([O-])=O TYJJADVDDVDEDZ-UHFFFAOYSA-M 0.000 description 1
- 235000019353 potassium silicate Nutrition 0.000 description 1
- 125000002572 propoxy group Chemical group [*]OC([H])([H])C(C([H])([H])[H])([H])[H] 0.000 description 1
- QQONPFPTGQHPMA-UHFFFAOYSA-N propylene Natural products CC=C QQONPFPTGQHPMA-UHFFFAOYSA-N 0.000 description 1
- 125000004805 propylene group Chemical group [H]C([H])([H])C([H])([*:1])C([H])([H])[*:2] 0.000 description 1
- 229940048084 pyrophosphate Drugs 0.000 description 1
- 229920006395 saturated elastomer Polymers 0.000 description 1
- 150000003333 secondary alcohols Chemical class 0.000 description 1
- 238000002791 soaking Methods 0.000 description 1
- 235000015424 sodium Nutrition 0.000 description 1
- FQENQNTWSFEDLI-UHFFFAOYSA-J sodium diphosphate Chemical compound [Na+].[Na+].[Na+].[Na+].[O-]P([O-])(=O)OP([O-])([O-])=O FQENQNTWSFEDLI-UHFFFAOYSA-J 0.000 description 1
- RYYKJJJTJZKILX-UHFFFAOYSA-M sodium octadecanoate Chemical compound [Na+].CCCCCCCCCCCCCCCCCC([O-])=O RYYKJJJTJZKILX-UHFFFAOYSA-M 0.000 description 1
- 229940048086 sodium pyrophosphate Drugs 0.000 description 1
- 229910000031 sodium sesquicarbonate Inorganic materials 0.000 description 1
- 235000018341 sodium sesquicarbonate Nutrition 0.000 description 1
- 235000019351 sodium silicates Nutrition 0.000 description 1
- 235000010339 sodium tetraborate Nutrition 0.000 description 1
- 239000004328 sodium tetraborate Substances 0.000 description 1
- MWNQXXOSWHCCOZ-UHFFFAOYSA-L sodium;oxido carbonate Chemical compound [Na+].[O-]OC([O-])=O MWNQXXOSWHCCOZ-UHFFFAOYSA-L 0.000 description 1
- 239000007787 solid Substances 0.000 description 1
- 238000005507 spraying Methods 0.000 description 1
- 230000000087 stabilizing effect Effects 0.000 description 1
- 125000004079 stearyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 description 1
- 239000003760 tallow Substances 0.000 description 1
- 235000019818 tetrasodium diphosphate Nutrition 0.000 description 1
- 239000001577 tetrasodium phosphonato phosphate Substances 0.000 description 1
- 239000004408 titanium dioxide Substances 0.000 description 1
- UNXRWKVEANCORM-UHFFFAOYSA-I triphosphate(5-) Chemical compound [O-]P([O-])(=O)OP([O-])(=O)OP([O-])([O-])=O UNXRWKVEANCORM-UHFFFAOYSA-I 0.000 description 1
- WCTAGTRAWPDFQO-UHFFFAOYSA-K trisodium;hydrogen carbonate;carbonate Chemical compound [Na+].[Na+].[Na+].OC([O-])=O.[O-]C([O-])=O WCTAGTRAWPDFQO-UHFFFAOYSA-K 0.000 description 1
- 239000012588 trypsin Substances 0.000 description 1
- 229960001322 trypsin Drugs 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C11—ANIMAL OR VEGETABLE OILS, FATS, FATTY SUBSTANCES OR WAXES; FATTY ACIDS THEREFROM; DETERGENTS; CANDLES
- C11D—DETERGENT COMPOSITIONS; USE OF SINGLE SUBSTANCES AS DETERGENTS; SOAP OR SOAP-MAKING; RESIN SOAPS; RECOVERY OF GLYCEROL
- C11D3/00—Other compounding ingredients of detergent compositions covered in group C11D1/00
- C11D3/02—Inorganic compounds ; Elemental compounds
- C11D3/04—Water-soluble compounds
- C11D3/08—Silicates
-
- C—CHEMISTRY; METALLURGY
- C11—ANIMAL OR VEGETABLE OILS, FATS, FATTY SUBSTANCES OR WAXES; FATTY ACIDS THEREFROM; DETERGENTS; CANDLES
- C11D—DETERGENT COMPOSITIONS; USE OF SINGLE SUBSTANCES AS DETERGENTS; SOAP OR SOAP-MAKING; RESIN SOAPS; RECOVERY OF GLYCEROL
- C11D3/00—Other compounding ingredients of detergent compositions covered in group C11D1/00
- C11D3/02—Inorganic compounds ; Elemental compounds
- C11D3/04—Water-soluble compounds
- C11D3/06—Phosphates, including polyphosphates
-
- C—CHEMISTRY; METALLURGY
- C11—ANIMAL OR VEGETABLE OILS, FATS, FATTY SUBSTANCES OR WAXES; FATTY ACIDS THEREFROM; DETERGENTS; CANDLES
- C11D—DETERGENT COMPOSITIONS; USE OF SINGLE SUBSTANCES AS DETERGENTS; SOAP OR SOAP-MAKING; RESIN SOAPS; RECOVERY OF GLYCEROL
- C11D3/00—Other compounding ingredients of detergent compositions covered in group C11D1/00
- C11D3/16—Organic compounds
- C11D3/37—Polymers
- C11D3/3746—Macromolecular compounds obtained by reactions only involving carbon-to-carbon unsaturated bonds
- C11D3/3757—(Co)polymerised carboxylic acids, -anhydrides, -esters in solid and liquid compositions
- C11D3/3761—(Co)polymerised carboxylic acids, -anhydrides, -esters in solid and liquid compositions in solid compositions
-
- C—CHEMISTRY; METALLURGY
- C11—ANIMAL OR VEGETABLE OILS, FATS, FATTY SUBSTANCES OR WAXES; FATTY ACIDS THEREFROM; DETERGENTS; CANDLES
- C11D—DETERGENT COMPOSITIONS; USE OF SINGLE SUBSTANCES AS DETERGENTS; SOAP OR SOAP-MAKING; RESIN SOAPS; RECOVERY OF GLYCEROL
- C11D3/00—Other compounding ingredients of detergent compositions covered in group C11D1/00
- C11D3/16—Organic compounds
- C11D3/38—Products with no well-defined composition, e.g. natural products
- C11D3/386—Preparations containing enzymes, e.g. protease or amylase
- C11D3/38609—Protease or amylase in solid compositions only
Landscapes
- Chemical & Material Sciences (AREA)
- Life Sciences & Earth Sciences (AREA)
- Engineering & Computer Science (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Oil, Petroleum & Natural Gas (AREA)
- Wood Science & Technology (AREA)
- Organic Chemistry (AREA)
- Inorganic Chemistry (AREA)
- Detergent Compositions (AREA)
Abstract
ABSTRACT OF THE DISCLOSURE
A powdered dishwashing composition containing a mixture of protease enzyme and anamylase enzymes have been found to be very useful in the cleaning of dishware. The compositions contain nonionic surfactants, at least one builder salt, and an alkali metal silicate and optionally a bleaching agent.
A powdered dishwashing composition containing a mixture of protease enzyme and anamylase enzymes have been found to be very useful in the cleaning of dishware. The compositions contain nonionic surfactants, at least one builder salt, and an alkali metal silicate and optionally a bleaching agent.
Description
20~853 IR 4600~
IMPROVED PHOSPHATE-CONTAINING POWDER AUTOMATIC DISHWAS~IING
COMPOSITION WITH ENZ~MES
BACKGROUND OF THE INVENTION
It has been found to be very useful to have enzymes in dishwashing detergent compositions because enzymes are very effective in removing food soils from the surface of glasses, dishes, pots, pans and eating utensils. The enzymes attack these materials while other components of the detergent will effect other aspects of the cleaning action. However, in order for the enzymes to be highly effective, the composition must be chemically stable, and it must maintain an effective activity at the operating temperature of the automatic dishwasher. Chemical stability such as to bleach agents is the property whereby the detergent composition containing enzymes does not undergo any significant degradation during storage. Activity is the property of maintaining enzyme activity during usage. From the time that a detergent i9 packaged until it is used by the customer, it must remain stable. Furthermore, during customer usage of the dishwashing detergent, it must retain its activity. Unle,ss the enzymes in the detergent are maintained in a minimum exposure to moisture and water, the enzymes will suffer a degradation during storage which will result in a product that will have a decreased activity. When enzymes are a part of ~he detergent composition, it has been found that the initial water content of the components of the composition should be as low a lev~l 20fi~8~3 d9 possible, and this low water content must be maintained during storage, since water will in the alkaline product deactivate the enzymes. This deactivation will cause a decrease in the initial activity of the detergent composition.
After the detergent container is opened, the detergent will be exposed to the environment which contains moisture.
During each instance that the detergent is exposed to the environment it could possibly absorb some moisture. This absorption occurs by components of the detergent composition absorbing moisture, when in contact with the atmosphere. This effect is increased as the container is emptied, since there will be a greater volume of air in contact with the detergent, and thus more available moisture to be absorbed by the detergent composition. This will usually accelerate the decrease in the activity of the detergent composition. The most efficient way to keep a high activity is to start with an initi.al high activity of enzyme and to use components in the dishwashing composition which do not interact with the enzyme or which have a low water affinity which will minimize any losses in activity as the detergent is being stored or used.
Powdered detergent compositions which contain enzymes can be made more stable and to have a high activity, if the initial free water content of the detergent composition is less than 10 percent by weight, more preferably less than 9 percent by weight and most preferably less than 8 percent by weight. Furthermore, the pH of a 1.0 wt% aqueous solution of the powdered detergent composition should be less than 11.0 more preferably less than 10.6, and most preferably less than 10.3. This low alkalinity of the dishwashing detergent should 2~8~3 maintain the stability of the detergent compositlon which contains a mixture of enz~mes, thereby providing a higher initial activity of the mixture of the enzymes and the maintenance of this initial high activity. A major concern in the use of automatic dishwashing compositions is the formulation of automatic dishwashing compositions which have a low alkalinity and can operate at a high temperature while maintaining superior cleaning performance and dish care. The present invention teaches the preparation and use of powdered automatic dishwashing compositions which are phosphate-containing and have superior cleaning performance and dish care, and are used at operating temperatures of 100F to 140F.
SUMMARY OF THE INVENTION
This invention is directed to producing powdered phosphate, enzyme-containing automatic dishwashing detergent compositions that have an increased chemical stability and essentially a high activity at wash operating temperatures of 40C to 65C (104F to about 150F), wherein the composition also can be used as a laundry pre-soaking agent. This is accomplished by controlling the alkalinity of the detergent composition and using a unique mixture of enzymes. An alkali metal silicate i9 used in the powdered dishwashing detergent compositions. The preferred builder system of the instant compositions comprises at least one phosphate builder salt which can be used in conjunction with polymeric builder salts and non-phosphate containing builder salts.
It is to be understood that the term powder in this invention includes within its definition tablets, soluble 2~6~8~3 capsules and soluble sachet. It is also possible to use the instant compositions as a laundry presoaking powder.
Conventional powdered automatic dishwashing compositions usually contain a low foaming surface-active agent, a chlorine bleach, alkaline builder materials, and usually minor ingredients and additives. The incorporation of chlorine bleaches requires special processing and storage precautions to protect composition components which are subject to deterioration upon direct contact with the active chlorine.
The stability of the chlorine bleach is also critical and raises additional processing and storage difficulties. In addition, it is known that automatic dishwasher detergent compositions may tarnish silverware and damage metal trim on china as a result of the presence of a chlorine-containing bleach therein. Accordingly, there is a standing desire to formulate detergent compositions for use in automatic dishwashing operations which are free of active chlorine and which are capable of providing overall hard surface cleaning and appearance benefits comparable to or better than active chlorine-containing detergent compositions. This reformulation is particularly delicate in the context of automatic dishwashlng operations, since during those operations, the active chlorine prevents the formation and/or deposition of tr~ublesome protein and protein-grease complexes on the hard dish surfaces and no surfactant system currently known is capable of adequately performing that function.
Various attempts have been made to formulate bleach-free low foaming detergent compositions for automatic dishwashing machines, containing particular low foaming nonionics, 2~8~3 ~uilders, filler materials and enzymes. US Patent 3,472,783 to Smille recognized that degradation of the enzyme can occur, when an enzyme is added to a highly alkaline automatic dlshwashing detergent.
French Patent No. 2,102,851 to Colgate-Palmolive, pertains to rinsing and washing compositions for use in automatic dishwashers. The compositions disclosed have a pH of 6 to 7 and contain an amylolytic and, if desired, a proteolytic enzyme, which have been prepared in a special manner from animal pancreas and which exhibit a desirable activity at a pH
in the range of 6 to 7. German Patent No. 2,038,103 to Henkel ~ Co. relates to aqueous licluid or pasty cleaning compositions containing phosphate salts, enzymes and an enzyme stabilizing compound. US Patent No. 3,799,879 to Francke et al, teaches a detergent composition for cleaning dishes, with a pH of from 7 to 9 containing an amylolytic enzyme, and in addition, optionally a proteolytic enzyme.
US Patent 4,101,457, to Place et al., teaches the use of a proteolytic enzyme having a maximum activity at a pH of 12 in an automatic dishwashing detergent.
US Patent 4,162,987, to Maguire et al., teaches a granular or licIuid automatic: dishwashing detergent which uses a proteolytic enzyme having a maximum activity at a pH of 12 as well as an amylolytic enzyme having a maximum activity at a pH
of 8.
US Patent No 3,827,938, to Aunstrup et al., discloses specific proteolytic enzymes ~hich exhibit high enzymatic activities in highly alkaline systems. Similar disclosures are found in British Patent Specification No. 1,361,386, to 2QS~53 ~OVO Terapeutis~ Laboratorium A/S. British Patent Specification No. 1,296,839, to Novo Terapeutisk Laboratorium A/S, discloses specific amylolytic enzymes which exhibit a high degree of enzymatic activity in alkaline systems.
Thus, while the prior art clearly recognizes the disadvantages of using aggressive chlorine bleaches in automatic dishwashing operations and also suggests bleach-free compositions made by leaving out the bleach component, said art disclosures are silent about how to formulate an effective bleach-free powdered automatic dishwashing compositions capable of providing superior performance during conventional use .
US Patent Nos. 3,821,118 and 3,840,480; 4,568,476, 4,501,681 and 4,692,260 teach the use of enzymes in automatic dishwashing detergents, as well as Belgian Patent 895,459;
French Patents 2,544,393 and 1,600,256; European Patents 256,679; 266,904; 271,155; 139,329; and 135,226; and Great Britain Patent 2,186,884.
The aforementioned prior art fails to provide a stable powdered automatic dishwashing detergent which is phosphate-containing and contains a mixture of enzymes as well as optionally, a peroxygen compound with a.n activator for the simultaneous degradation of both proteins and starches, wherein the combination of anylase and protease enzymes have a maximum activity at a pH of less than 11.0 and the powdered automatic dishwashing detergent has high cleaning performance in a temperature range of 40C to 65C (104F to 150F). It is an object of this invention to incorporate a novel enzyme mixture in a phosphate-containing, powdered automatic 2~S~8~3 ~ishwasher detergent composition for use in automatlc dishwashing operations capable of providing at least equal or better performance to conventional automatic dishwashing compositions at operating temperatures of 100F to 150F.
DETAILED DESCRIPTION
The present invention relates to a powdered automatic dishwashing detergent compositions which comprise a nonionic surfactant, alkali metal silicate, a phosphate-containing builder system, optionally, a peroxygen compound with an activator as a bleaching agent and a mixture of an amylase enzyme and a protease enzyme, wherein the powdered automatic dishwashing detergent composition has a pH of less than 11.0 and the powdered dishwashing detergent composition exhibits high cleaning efficiency for both proteins and starches at a wash temperature of 40C to 65C (100F to 150F).
The nonionic surfactants that can be used in the present powdered automatic dishwasher detergent compositions are well known. A wide variety of these surfactants can be used.
The nonionic synthetic organic detergents are generally described as ethoxylated propoxylated fatty alcohols which are low-foaming surfacl:ants and may be possibly capped, characterized by the presence of an organic hydrophobic group and an organic hydrophilic group and are typically produced by the condensation of an organic aliphatic or alkyl aromatic hydrophobic compound with ethylene oxide and/or propyleneoxide (hydrophilic in nature). Practically any hydrophobic compound having a carboxy, hydroxy, amide or amino group with a free hydrogen attached to the oxygen or the nitrogen can be condensed with ethylene oxide or propylene oxide or with the 20~t~853 polyhydration product thereof, polyethylene glycol, to form a nonionic detergent. The length of the hydrophilic or polyoxyethylene chain can be readily adjusted to achieve the desired balance between the hydrophobic and hydrophilic groups. Typical suitable nonionic surfactants are those disclosed in US Patent Nos. 4,316,812 and 3,630,929.
Preferably, the nonionic detergents that are used are the low-foaming polyalkoxylated lipophiles wherein the desired hydrophile-lipophile balance is obtained from addition of a hydrophilic poly-lower alkoxy group to a lipophilic moiety. A
preferred class of the nonionic detergent employed is the poly-lower alkoxylated higher alkanol wherein the alkanol is of 9 to 18 carbon atoms and wherein the number of moles of lower alkylene oxide (of 2 or 3 carbon atoms) is from 3 to 15.
Of such materials it is preferred to employ those wherein the higher alkanol is a high fatty alcohol of 9 to 11 or 12 to 15 carbon atoms and which contain from 5 to 15 or 5 to 16 lower alkoxy groups per mole. Preferably, the lower alkoxy is ethoxy but in some instances, it may be desirably mixed with propoxy, the latter, if present, usually being ma~or (more than 50~) portion. Exemplary of such compounds are those wherein the alkanol i9 of 12 to 15 carbon atoms and which contaln about 7 ethylene oxide groups per mole.
Useful nonionics are represented by the low foam Plurafac series from BASF Chemical Company which are the reaction product of a higher linear alcohol and a mixture of ethylene and propylene oxides, containing a mixed chain of ethylene oxide and propylene oxide, terminated by a hydroxyl group.
~xamples include Product A(a C~3- Cls fatty alcohol condensed 2 ~3 6 ~ 8 r~ 3 ~ith 6 moles ethylene oxide and 3 moles propylene o~ide).
Product B (a 13-Cls fatty alcohol condensed with 7 mole propylene oxide and 4 mole ethylene oxide), and Product C (a C13- C15 fatty alcohol condensed with 5 moles propylene oxide and 10 moles ethylene oxide). Another group of liquid nonionics - are available from Shell Chemical Company, Inc. under the Dobanol t~ademark: Dobanol 91-5 is a low foam ethoxylated Cg-Cl1 fatty alcohol with an average of 5 moles e~hylene oxide and Dobanol 25-7 is an ethoxylated Cl2-Cl5 fatty alcohol with an average of 7 moles ethylene oxide. Another liquid nonionic surfactant that can be used is sold under the tradename Lutensol SC 9713.
Poly-Tergent nonionic surfactants from Olin Organic Chemicals such as Poly-Tergent SLF-18, a biodegradable, low-foaming surfactant is specially preferred for the powdered automatic dishwasher detergent compositions of this instant invention. Poly-Tergent SLF-la, a water dispersible having a low cloud point, has lower surface tension and lower foaming is very suitable for automatic dishwasher detergent.
Synperonic nonionic surfactants from ICI such as Synperonic LF/D25, LF/RA30 are especially preferred nonionic surfactants that can be used in the powdered automatic dishwasher detergent compositi.ons of the instant invention. Poly-Tergent nonionic surfactants from Olin Organic Chemicals such as Poly-Tergent SLF-18, a biodegradable, low-foaming surfactant is specially preferred for the powdered automatic dishwasher detergent compositions of this instant invention. Poly-Tergent SLF 18, a water dispersible, having a low cloud point nas lower surface tension and lower foaming is very sultable for automatic dishwasher detergent Other useful surfactan~s are Neodol 25-7 and Neodol 23-6.5, which products are made by Shell Chemical Company, Inc.
The former is a condensation product of a mixture of higher fatty alcohols averaging about 12 to 13 carbon atoms and the number of ethylene oxide groups present averages 6.5. The hlgher alcohols are primary alkanols. Other examples of such detergents lnclude Tergitol 15-S-7 and Tergitol 15-S-9 (registered trademarks), both of which are linear secondary alcohol ethoxylates made by Union Carbide Corp. The former is mixed ethoxylation product of 11 to 15 carbon atoms linear secondary alkanol with seven moles of ethylene oxide and the latter i9 a similar product but with nine moles of ethylene oxide being reacted.
Also useful in the present compositions as a component of the nonionic detergent are higher molecular weight nonionics, such as Neodol 45-11, which are similar ethylene oxide condensation products of higher fatty alcohols, with the higher fatty alcohol being of 14 to 15 carbon atoms and the number of ethylene oxide groups per mole being 11. Such products are also made by Shell Chemical Company.
In the preferred poly-lower alkoxylated higher alkanols, to obtain the best balance of hydrophilic and lipophilic moieties the number of lower alkoxies will usually be from 40%
to 100% of the number of carbon atoms in the higher alcohol, preferably 40 to 60% thereof and the nonionic detergent will preferably contain at least 50% of such preferred poly-lower alkoxy higher alkanol.
The alkyl polysaccharides are surfactants which are also useful alone or in conjunction with the aforementioned surfactants and those having a hydrophobic group containing from 8 to 20 carbon atoms, preferably from 10 to 16 carbon atoms, most preferably from 12 to 14 carbon atoms, and polysaccharide hydrophilic group containing from 1.5 to 10, preferably from 1.5 to 4, and most preferably from 1.6 to 2.7 saccharide units (e.g., galactoside, glucoside, fructoside, glucosyl, fructosyl, and/or galactosyl units). Mixtures of saccharide moieties may be used in the alkyl polysaccharide surfactants. The number x indicates the number of saccharide units shown later in a particular alkyl polysaccharide surfactant formula. For a particular alkyl polysaccharide molecule x can only assume integral values. In any physical sample can be characterized by the average value of x and this average value can assume non-integral values. In this specification the values of x are to be understood to be average values. The hydrophobic group (R) can be attached at the 2-, 3-, or 4- positions rather than at the l-position, (thus giving e.g. a glucosyl or galactosyl as opposed to a glucoside or galactoside). However, attachment through the 1-position, i.e., glucosides, galactosides, fructosides, etc., i9 preferred. In the preferred product the additional saccharide units are predominately attached to the previous saccharide unit's 2-position. Attachment through the 3-, 4-, and 6-positions can also occur. Optionally and less desirably there can be a polyalkoxide chain joining the hydrophobic moiety (R) and the polysaccharide chain. The preferred alkoxide moiety is ethoxide.
2 ~ 3 Typical hydrophobic groups include alkyl groups, either ~ saturated or unsaturated, branched or unbranched containing - from 8 to 20, preferab]y from 10 to 16 carbon atoms.
Preferably, the alkyl group is a straight chain saturated alkyl group. The alkyl group can contain up to 3 hydroxy groups and/or the polyalkoxide chain can contain up to about 30, preferably less than 10, alkoxide moieties.
Suitable alkyl polysaccharides are decyl, dodecyl, tetradecyl, pentadecyl, hexadecyl, and octadecyl, di-, tri-, tetra-, penta-, and hexaglucosides, galactosides, lactosides, fructosides, fructosyls, lactosyls, glucosyls and/or galactosyls and mixtures thereof.
The alkyl monosaccharides are relatively less soluble in water than the higher alkyl polysaccharides. When used in admixture with alkyl polysaccharides, the alkyl monosaccharides are solubilized to some extent. The use of alkyl monosaccharides in admixture with alkyl polysaccharides is a preferred mode of carrying out the invention. Suitable mixtures include coconut alkyl, di-, tri-, tetra-, and pentaglucosides and tallow alkyl tetra-, penta-, and hexaglucosides.
The preferred alkyl polysaccharides are alkyl polyglucosides having the formula:
R2O(CnH2nO)r(z)~
wherein Z is derived from glucose, R i9 a hydrophobic group selected from the group consisting of alkyl, alkylphenyl, hydroxyalkylphenyl, and mixtures thereof in which said alkyl groups contain from 10 to 18, preferably from 12 to 14 carbon atoms; n is 2 or 3 preferably 2, r is from 0 to 10, preferable 2Q$~3 0; and x is from 1.5 to 8, preferably from 1 5 to ~, most preferably from 1.6 to 2.7. To prepare these compounds a long chain alcohol (R2OH) can be reacted with glucose, in the presence of an acid catalyst to form the desired glucoside.
Alternatively the alkyl polyglucosides can be prepared by a two step procedure in which a short chain alcohol (RIOH) an be reacted with glucose, in the presence of an acid catalyst to form the desired glucoside. Alternatively the alkyl polyglucosides can be prepared by a two step procedure in which a short chain alcohol (Cl6) is reacted with glucose or a polyglucoside (x=2 to 4) to yield a short chain alkyl glucoside (x=1 to 4) which can in turn be reacted with a longer chain alcohol (R2OH) to displace the short chain alcohol and obtain the desired alkyl polyglucoside. If this two step procedure is used, the short chain alkylglucoside content of the final alkyl polyglucoside material should be less than 50~, preferably less than 10~, more preferably less than 5~, most preferably 0% of the alkyl polyglucoside.
The amount of unreacted alcohol (the free fatty alcohol content) in the desired alkyl polysaccharide surfactant is preferably less than 2~, more preferably less than 0.5% by weight of the total of the alkyl polysaccharide. For some uses it is desirable to have the alkyl monosaccharide content less than about 10~.
The used herein, "alkyl polysaccharide surfactant" is intended to represent both the preferred glucose and galactose derived surfactants and the less preferred alkyl polysaccharide surfactants. Throughout this specification, "alkyl polyglucoside" is used ~o include alkyl polyglycosides 2 ~ 3 oecause the stereo chemistry of the saccharide moiety is changed during the preparation reaction.
An especially preferred APG glycoside surfactant is APG
625 glycoside manufactured by the E~enkel Corporation of Ambler, PA. APG 625 is a nonionic alkyl polyglycoside characterized by the formula:
CnH2n+,0 (C6HI005) lH
wherein n=10(2~); n=12(65~); n=14(21-28%); n=16(4-8~) and n=18(0.5~) and x(degree of polymerization) = 1.6. APG 625 has: a pH of 6-~(10~ of APG 625 in distilled water); a specific gravity at 25F of 1.1 grams/ml; a density at 25F of 9.1 kgs/gallons; a calculated HLB of 12.1 and a Brookfield viscosity at 35C, 21 spindle, 5-10 RPM of 3,000 to 7,000 cps.
Mixtures of two or more of the liquid nonionic surfactants can be used and in some cases advantages can be obtained by the use of such mixtures.
The liquid nonaqueous nonionic surfactant is absorbed on a builder system which comprises a phosphate-containing particles which is a builder salt and optionally a low 2~ molecular weight polyacrylate type polymer such as a polyacrylate organic and/or inorganic detergent builders as well as phosphate-free builder salts such as an alkali carbonate such as sodium carbonate or sodium citrate or a mixture of sodium carbonate and sodium citrate. A preferred solid builder salt is an alkali metal polyphosphate such as sodium tripolyphosphate ("TPP"). The TPP is a blend of anhydrous TPP and a small amount of TPP hexahydrate such that the chemically bound water content is 1~, which corresponds to about one H20 per pentasodium tripolyphosphate molecule. Such g ~ 3 ~P may be produced by treating anhydrous TPP with a limited amount of water. The presence of the hexahydrate slows down the rapid rate of solution of the TPP in the wash bath and inhibits caking. One suitable TPP is sold under the name Thermphos NW. The particles size of the Thermphos NW TPP, as supplied, usually averages about 200 microns with largest particles being about 400 microns. In place of all or part of the alkali metal polyphosphate one or more other detergent builder salts can be used. Suitable other builder salts are alkali metal carbonates, borates, phosphates, bicarbonates, silicates, lower polycarboxylic acid salts, and polyacrylates, polymaleic anhydrides and copolymers of polyacrylates and polymaleic anhydrides and polyacetal carboxylates.
Specific examples of such builders are sodium carbonate, potassium carbonate, sodium tetraborate, sodium pyrophosphate, sodium bicarbonate, sodium hexametaphosphae, sodium sesquicarbonate, sodium mono and diorthophosphate, and potassium bicarbonate. The builder salts can be used alone with the nonionic surfactant or in an admixture with other builders. Typical builders also include those disclosed in U.S. Pat Nos. 4,316,812, 4,264,466 and 3,630,929 and those disclosed in U.S. Pat Nos. 4,144,226, 4,135,092 and 4,146,495, all of which are herein incorporated by reference.
Other phosphate-free builder salts which can be mixed with the phosphate containing builder salts are gluconates, phosphonates, and nitriloacetic acid salts in conjunction with the builder salts are optionally used a low molecular weight polyacrylates having a molecular weight of 1,000 to 100,000, more preferably about 2,000 to about 80,000. A preferred low 2~8~3 ~.olecular weiyht polyacrylate is Sokalan~nCP45 or Sokalan~CP5 manufactured by BASF and having a molecular weight of 70,000.
Another preferred low molecular weight polyacrylate is Acrysol~LMW45ND manufactured by Rohm and Haas and having a molecular weight of 4,500. NorasolTMWL2 comprises 26~ LMW45ND
sprayed on 74~ soda ash.
Sokalan~CP45 or CP5 is a copolymer of an acrylic acid and maleic acid anhydride. Such a material should have a water absorption at 38C and 78 percent relative humidity of less than about 40 percent and preferably less than 30 percent.
The builder is commercially available under the tradename of Sokalan~CP45. This is a partially neutralized copolymer of acrylic acid and maleic anhydride sodium salt. Sokalan~CP5 is classified as a suspending and anti-deposition agent. This suspending agent has a low hygroscopicity. Another builder salt is Sokalan~MCP5 having a molecular weight of 70,000 which is a completely neutralized version of CP45. An ob~ective i9 to use suspending and anti-redeposition agents that have a low hygroscopicity. Copolymerized polyacids have this property, and particularly when partially neutralized. ~cusol~'64ND
provided by Rohm Haas is another useful suspending agent.
Another class of builders useful herein are the aluminosilicates, both of the crystalline and amorphous type.
Various crystalline zeolites (i.e. alumino-silicates) are described in British Patent No. 1,504,168, U.S. Patent No.
4,409,136 and Canadian Patent Nos. 1,072,835 and 1,087,477.
An example of amorphous zeolites useful herein can be found in Belgium Patent No. 835,351. The zeolites generally have the formula 20~53 (M2O)~(Al~O3)y(SiO2)x wH2O
wherein x is 1, y is from 0.8 to 1.2 and preferably 1, z is from 1.5 to 3.5 or higher and preferably 2 to 3 and w is from 0 to 9, preferably 2.5 to 6 and M is preferably sodium. A
typical zeolite is type A or similar structure, with type 4A
particularly preferred. The preferred aluminosilicates have calcium ion exchange capacities of 200 milliequivalents per gram or greater, e.g. 400 meq/g.
The alkali metal silicates are useful anti-corrosion agents which function to make the composition anti-corrosive to eating utensils and to automatic dishwashing machine parts.
Sodium silicates of Na2O:SiO2 ratios of from 1:1 to 1:2.4.
Potassium silicates of the same ratios can also be used. The preferred silicates are sodium disilicate and sodium metasilicate.
Essentially, any compatible anti-foaming agent can be used. Preferred anti-foaming agents are silicone anti-foaming agents. The~e are alkylated polysiloxanes and include polydimethyl siloxanes, polydiethyl siloxanes, polydibutyl siloxanes, phenyl methyl siloxanes, trimethysilanated silica and triethylsilanated silica. A suitable anti-foaming agent is Silicone TP-201 from Union Carbide. Other suitable anti-foaming agents are Silicone DB700, DB100 used at 0.2 to 1.0 percent by weight, sodium stearate used at a concentration level of 0.5 to 1.0 weight percent and 1.0 weight percent, and LPKn 158 (phosphoric ester) sold by Hoechst used at a concentration level of 0 to 1.5 weight percent, more preferably 0.1 to 1.0 weight percent. The perfumes that can be used include lemon perfume and other natural scents.
2~8~3 _ssentially, any opacifier that is compatible with the remaining components of the detergent formulation can be used.
A useful and preferred opacifier is titanium dioxide at a concentration level of 0 to 1.0 weight percent.
A key aspect is to keep the free water (non-chemically bounded water) in the detergent composition at a minimum.
Absorbed and adsorbed water are two types of free water, and comprise the usual free water found in a detergent composition. Free water will have the affect of deactivating the enzymes.
The detergent composition of the present invention can include a peroxygen bleaching agent at a concentration level of 0 to 20 weight percent, more preferably 0.5 to 17 weight percent and most preferably at 1.0 to 14 weight percent. The oxygen bleaching agents that can be used are alkali metal perborates, percarbonate, perphthalic acid, perphosphates, and potassium monopersulfate. A preferred compound is sodium perborate monohydrate and dihydrate. The peroxygen bleaching compound is preferably used in admixture with an activator thereof at a concentration level of 1 to about 5 weight percent. Suitable activators are those disclosed in U.S.
Patent No. 4,264,466 or in column 1 of U.S. Patent No.
4,430,244. Polyacetylated compounds are preferred activators.
Suitable preferred activators are tetraacetyl ethylene diamine ("TAED"), pentaacetyl glucose and ethylidenebenzoate acitate.
The activator usually interacts with the peroxygen compound to form a peroxyacid bleaching agent in the wash water.
2~6$8~3 The detergent formulation also contains a mixture of a protease enzyme and an amylase enzyme and, optionally, a lipase enzyme that serve to attack and remove organic residues on glasses, plates, pots, pans and eating utensils. Lipolytic enzymes can also be used in the powdered automatic dishwasher detergent composition. Proteolytic enzymes attack protein residues, lipolytic enzymes fat residues and amylolytic enzymes starches. Proteolytic enzymes include the protease enzymes subtilisn, bromelin, papain, trypsin and pepsin.
Amylolytic enzymes include amylase enzymes. Lipolytic enzymes include the lipase enzymes. The preferred amylase enzyme is available under the name Maxamyl, derived from Bacillus licheniformis and is available from Gist-brocades of the Netherlands in the form of a prill having an activity of about 5,000 TAU/g. One of the preferred protease enzyme is available under the name Maxapem 15, 20, 30 or Maxapem 42 which is a high alkaline mutant proteolytic enzyme derived from Bacillus acalophylus, and is available from Gist-Brocades, of the Netherlands in a prill form (activity of about 15, 20, 30 or 40 MPU/g). Preferred enzyme activates per wash are Maxapem 10-100 MPU/g per wash and Maxamyl 625 to 4,000 TAU/g per wash. Another preferred protease enzyme is available under the name Maxatase derived from a novel Bacillus strain designated "PB92" wherein a culture of the Bacillus is deposited with the laboratory for Microblology of the Technical University of Delft and has a number R-60, and ls available from Gist-Brocades, of the Netherlands in prill form (activity of about 440 KDU/g). Preferred enzyme activates per wash are Maxatase 200-700 KDU/g per wash.
2~98~3 The weight ratio of the proteolytic enzyme to the amylolytic en~yme in the powdered automatlc dishwasher detergent compositions is 8:1 to 1:1, and more preferably 4.5:1 to l.1:1.
The detergent composition can have a fairly wide ranging composition. The surfactant can comprise 0 to 15 percent by weight of the composition, more preferably 0.1 to 15 percent by weight, and most preferably 1 to 12 percent by weight. The soil suspending agent which is preferably a copolymerized polyacrylic acid will be present in an amount of 0 to 20 percent by weight, more preferably 3 to 15 percent by weight and most preferably 5 to 15.0 percent by weight. The anti-foaming agent will be present in an amount of 0 to 1.5 percent by weight, more preferably 0.1 to 1.2 percent by weight and most preferably 0.3 to 1 percent by weight. The builder system, which is preferably an alkali metal tripolyphosphate and/or an alkali metal pyrophosphate, is present in an amount of 2 to 40 percent by weight, more preferably about 4 to about 40 percent by weight and most preferably 5 to 35 percent by weight for a standard product. However, for a concentrated formula, the alkali metal tripolyphosphate is present in an amount of 10 to 65 weight percent, more preferably 15 to 65 by weight, and most preferably 15 to 62~ by weight percent.
The builder system can also contain a low molecular weight polyacrylate type polymer at a concentration level of 0 to 20 w~ight percent, more preferably 1.0 to 17 weight percent and most preferably about 2 to 14 w~ight percent.
The alkali silicate, which is a corrosion inhibitor, wherein sodium disilicate is preferred, will be present in an 2~.9~3 ~ mount of 0 to 30 percent by weight, more preferably 3 to 30 percent by weight and most preferably 4 to 28 percent by weight.
The opacifier will be present in an amount of 0 to 1.0 percent by weight, more preferably about 0.1 to 7 percent by weight and most preferably 0.4 percent by weight.
The enzymes will be present in a prilled form as supplied by Gist Brocades at a concentration of 0.8 to 22.0 percent by weight, more preferably 0.9 to 20.0 percent by weight, and most preferably 1.0 to about 18.0 percent by weight. The protease enzyme prills in the automatic dishwashing composition will about 0.5 to 15.00 percent by weight, more preferably 0.7 to 13.0 weight percent and most preferably 0.8 to 11.0 percent by weight. The amylase enzyme prills will comprise 0.3 to 8.0 percent by weight, more preferably 0.4 percent to 7.0 weight percent and most preferably 0.5 to 6.0 weight percent. The lipase enzyme prills will comprise 0.00 to 8.0 percent by weight of the detergent composition. A
typical lipase enzyme is Lipolas 100 T from NOVO Nordisk of Denmark. The lipase enzymes are especially beneficial in reducing grease residues and related filming problems on glasses arld dishware. Another useful lipase enzyme is Amaneo PS lipase provided by Amaneo International Enzyme Co., Inc.
Other components such as perfumes will comprise about 0.1 to about 5.0 percent by weight of the detergent composition.
One method of producing the detergent powder formulation consisting first of spraying and absorbing nonionic surfactant into the phosphate and carbonate builder salts and mixed thoroughly in a rotary drum. The absorbed builder salt was ~Q~53 hen aged overnight to completely absorb the nonionic to form a free flowing powder which was then mixed with sodium sulfate and silicate in a twin-shelled blender. Finally, enzyme prills were added and mixed thoroughly to form a free flowing detergent powder. Another method of producing the powder detergent forl~ulation having a bulk density of 0.9 is to spray dry by any conventional means the nonionic surfactant and defoamer into the perborate bleach compound and the builder salt. This spray dry materials can be used immediately, but it is preferred to age then for 24 hours. The spray dried materials are dry blended in any suitable conventional blender such as a tumble blender at about room temperature with the other ingredients of the composition until a homogenous blend is obtained.
The instant compositions also can be produced as low density powders according to the procedure as set forth in U.S. Patent 4,931,203, wherein these powders have a bulk density 1/3 less than the bulk density of the bulk density of the standard powders which have a bulk density of 1.0 kg/liter.
The concentrated powdered nonionic automatic dishwashing detergent compositions of the present invention disperses readily in the water in the dishwashing machine. The presently used home dishwashing machines have a measured capacity for 80cc or 90 grams of detergent. In normal use, for example, for a full load of dirty dishes 60 grams of powdered detergent are normally used.
In accordance with the present invention only about 56cc or about 50 grams of the standard powdered detergent 2QS~3 omposition is needed whereas the dose of concentrated detergent is 33 g weight. The normal operation of an automatic ~ishwashing machine can involve the following steps or cycles: washing, rinse cycles with cold/hot water and rinse cycles with hot water. The entire wash and rinse cycles require 60 minutes. The temperature of the wash water is 40C
to 65C and the temperature of the rinse water is 55C to 65C. The wash and rinse cycles use about 4 to 7.5 liters of water for the wash cycle and about 4 to 7.5 liters of water for the hot rinse cycle.
The concentrated powdered automatic dishwashing detergent compositions exhibit excellent cleaning properties and because of the high concentration of the detergent in the composition, the detergent is not totally consumed during the wash cycle or totally eliminated during the rinse cycle such that there i9 a sufficient amount of detergent remaining during the rinse cycle to substantially improve the rinsing. The washed and dried dishes are free of undesirable traces, deposits or film due to the use of hard water in the rinse cycle.
DESCRIPTION OF THE PREFERRED EMBODIMENTS
Example 1 Standard Density Powder Auto-Dish Detergent Composition A free flowing, highly soluble standard density powder auto-dish detergent was developed by absorbing nonionic surfactant (Union Carbide Tergitol MDS-42) on highly absorptive sodium tripolyphosphate (Oxy Chem HRS3342). High 2~6~8~
,oluble sodium silicate (PQ Corporation ~IS 240), granular sodium sulfate (Kerr-McGee Corporation Trona), granular sodium carbonate (Allied Chemical dense soda ash) were also necessary to give necessary flow property and high solubility of the 5 detergent. Product was made by dry blending all the ingredients.
Table I
Ingredi~ Amount Concentration Sodium Tripolyphosphate (Oxychem HRS3342) 144g 36%
Anhydrous Sodium Sulfate-Trona Gran. 104 26 Anhydrous Sodium Carbonate-Allied Dense 88 Hydrated Sodium Silicate - PQ HS 240 48 12 Nonionic Surfactant - Tergitol MDS-42 16 Maxapem CX 30 MPU- Gist-Brocades 0 Maxamyl P 5000 - Gist-Brocades 0 400g 100%
Amount of Maxapem 30 and Maxamyl enzymes were incorporated in the powder ADD general formula as exemplified in Table I by replacing equivalent amount of sodium sulfate in the product.
Rest of the ingredients and the amount remained same in the product.
The finished product was aged over a period of two days to give a nice dry free-flowing powder. The product was tested with 50g dose using the ASTM spotting and filming teRt method combined with denatured egg soiled (egg yolk denatured with 2.5 M CaCl2 solution) along with haked-on oatmeal soiled substrates against non-enzyme powder ADD, bleach-containing powder ADD prototype and CASCADE, a commercial powder ADD with 50g dose and PALMOLIVE AUTOMATIC, a commercial 2 ~ 3 ~iquid ADD with 80g dose. Tne cleaning performance tests were run at 120F wash cycle temperatures using tap water (ca. 115 ppm water hardness).
2 0 ~ 3 Table II
Auto-Dish Performance (Enzyme V9. Non-Enzyme vs. Bleach-Based Product) In Tap Water at 120F Wash Cycle Temperature Auto-Dish Enzyme _Conc. %Dose g Performance, Cleaning Products Maxapem 30 Maxamyl Denatured Egg Baked-On Porridge 1 0 0 50g 6.5% 60.0 2 0 1 50g 30.5 99.5 3 2 0 50g 98.0 60.0 4 2 1.5 50g 99.0 99.5 2 0.5 50g 95.0 98.5 6 1.5 0.25 50g 94.0 95.5 7 1 0.5 50g 93.0 100.0 8 1 0.25 50g 94.5 100.0 9 1 0.25 50g 68.5 100.0 PADD 11614-9OB (contain 1.2~ Av.C1) 50g 91.5 60.0~
CASCADE Powder (contain 1% Av.Cl) 50g 63.0 25 60.0~
PALM AUTO Liq (contain 1~ Av.Cl) 80g 91.0 60.0~
Non-enzyme poser ADD Conrol (1) barely cleaned any egg and starch soil whereas incorporation of Protein Engineered 42 Maxacal and Maxamyl helped complete removal egg and starchy soil respectively. Enzymes (both Maxapem 30 and Maxamyl) containing powders (2-9) outperformed chlorine bleach containing ADDs like PADD 11614-9OB, CASCADE, a commercial powder and PALMOLIVE AUTOMATIC, a commercial Liquid in cleaning egg and starchy soil.
2 ~ 3 Table III
Auto-Dish Products ASTM Spotting/Filming Performance Data 300 ppm Water Hardness, 120F Wash Cycle Temperature Auto-Dish Products Spotting/Filming Powder Auto-Dish (3) 1st Cycle A 3 2nd Cycle A 3 3rd Cycle A 3,4 4th Cycle A 2,3 Powder ADD 11614-9OB (Chlorine Bleach) 1st Cycle 2nd Cycle B5 3rd Cycle B5 4th Cycle B 3,4 CASCADE Powder (Chlorine Bleach) 1st Cycle A 5 2nd Cycle A 6 3rd Cycle AB 6 4th Cycle A 3 PALMOLIVE AUTOMATIC Liquid (Chlorine Bleach) 1st Cycle BC 3,4 2nd Cycle CD 4 3rd Cycle D ~,5 4th Cycle DE 2,3 Spotting Scale:
A best- no spots B very few spots C approximately 25~ spot coverage D approximately 50~ spot coverage E excessive spots Filming Scale:
1 best - no film 2 slight film 3 noticeable film 4 significant film excessive film 4~
2 0 ~ 3 Rxample 2 According to the procedure of U.S. Patent 4,931,203 the following concentrated formulation was produced:
Table I~
Inqredients Concentration Sodium Tripolyphosphate Base Bead - D CP 151-627 Protein Sodium Carbonate (Allied Chemical Dense Soda Ash) 10.00 Sodium Metasilicate ( 1 Na2O: 1 SiO2, PQ Metsobeads 2048~.00 Sodium Silicate (1 Na2O: 1 SiO2, PQ Britesil LD24) 12.00 Nonionic Surfactant (Union Carbide Tergitol MDS-42) 6.00 Maxapem CX 30 (Gist-Brocades) 1.50 Maxamyl P 5,000 (Gist-Brocades) The finished product is aged over two days to give a nice dry free-flowing powder.
Laboratory performance of the compositions of ~xample 2 were carried out using multi-soils. This was done to show differences between the prototype formulations and commercial products. Egg soil was prepared by mixing egg yolk with an equal amount of 2.5 N calcium chloride solution. This mixture was applied as thin cross-wise film to the usable surface of 7.5 inch china plates. The plates were aged in 50~ relative humidity overnight. Oatmeal soil was prepared by boiling 24 grams of Quaker Oats in 400 ml of tap water for ten minutes.
Three grams of this mixture was spread as thin film onto a 7.5 inch china plate. The plates were aged for 2 hours at 80C.
They were then stored overnight at room temperature. Two plates of each egg and oatmeal were used per wash. The plates 2~8.~3 were placed in the same positions in the dishwasher. Thirty-three grams of the detergent was used as a single dose per wash. All plates were scored by measuring the percent area cleaned. The multi-soil cleaning test results are reported below. The results tabulated in Table V were average of at least 2 runs. Average results reflect the average performance results obtained in three different water conditions. The product was tested with 33g dose using the ASTM Method D3556-79 spotting and filming test method combined with denatured egg soiled (egg yolk denatured with 2.5 M CaCl2 solution) along with the 50g dose of commercial powder product. Enzyme containing prototype powder ADD completely removed egg soil and major portion of oatmeal, whereas, CASCADE, a commercial powder barely removed any of the egg and oatmeal soil.
Table V
Cleaning performance, Enzyme v9. non-Enzyme Based Product Product Dose ~Cleaninq Denatured Eqq Baked-On Oatmeal Conc. ADD Product (Example 2) 33g 100~ 100 CASCADE Powder (Commercial Product) 50g 40~ 50 2~8~3 Example 3 Standard Density Powder Auto-Dish Detergent Composition A free flowing, highly soluble standard density powder auto-dish detergent was developed by absorbing nonionic surfactant (Union Carbide Tergitol MDS-42) on highly absorptive sodium tripolyphosphate (Oxy Chem HRS3342). High soluble sodium silicate (PQ Corporation HS 240), granular sodium sulfate (~err-McGee Corporation Trona), granular sodium carbonate (Allied Chemical dense soda ash) were also necessary to give necessary flow property and high solubility of the detergent. Product was made by dry blending all the ingredients.
Table VI
Inqredients Amount Concentration Sodium Tripolyphosphate (Oxy Chem HRS3342) 144g36 Anhydrous Sodium Sulfate-Trona Gran. 10426 Anhydrous Sodium Carbonate-Allied Dense 8822 Hydrated Sodium Silicate - PQ HS 240 4312 Nonionic Surfactant - Tergitol MDS-42 16 4 Maxatase - Gist Brocades O O
Maxamyl P 5000 - Gist-Brocades 0 400g 100~
Amount of Maxatase P440,000 and Maxamyl P5,000 prilled enzymes were incorporated in the powder ADD general formula as exemplified in Table VI by replacing equivalent amount of sodium sulfate in the product. Rest of the ingredients and the amount remained same in the product.
The finished product was aged over a period of two days to give a nice dry free-flowing powder. The product was tested with 50g dose using the ASTM spotting and filming test method combined 2~853 .~ith denatured egg soiled (egg yolk denatured with 2.5 M CaClz solution) along with baked-on oatmeal soiled substrates against non-enzyme powder ADD, bleach-containing powder ADD prototype and a commercial (CASCADE) powder ADD with 50g dose and a commercial (PALMOLIVE AUTOMATIC) Liquid ADD with 80g dose. The cleaning performance tests were run at 120F wash cycle temperatures using tap water (ca. 115 ppm water hardness).
2~S~3 Table VII
Auto-Dish Performance (Enzyme vs. Non-Enzyme vs. Bleach-Based Product) In Tap Water at 120F Wash Cycle Temperature Auto-Dish Enzymes Conc. ~ Dose g Performance, ~ Cleaning Products Maxatase Maxamyl Denatured Egg Baked-On Porridge 1 0 0 50g 7.5 60.0 2 0 1 50g32.0 99.0 3 2 0 50g95.0 60.0 4 2 1.5 50g98.5 99.5 2 0.5 50g95.0 98.5 6 1.50.25 50g96.0 96.0 7 1 0.5 50g96.0 100.0 8 1 0.25 50g95.0 100.0 9 1 0.25 50g70.5 100.0 Powder ADD
11614-9OB (contain 1.2~ Av.Cl)50g 91.5 60.0 Commercial Powder (contain 1~ Av.Cl) 50g63.0 60.0 Commercial Liq (contain 1~ Av.Cl) 80g91.0 60.0 Non-enæyme poser ADD Conrol (1) barely cleaned any egg and starch soil whereas incorporation of Maxatase and Maxamyl helped complete removal egg and starchy soil respectively.
Enzymes (both Maxatase and Maxamyl) containing powders (2-9) outperformed chlorine bleach containing ADDs like PADD 11614-90B, commercial powder and commercial Liquid in cleaning egg and starchy soil.
2 ~
Table VIII
: Auto-Dish Products ASTM Spotting~Filming Performance Data 300 ppm Water Hardness, 120F Wash Cycle Temperature Auto-Dish Products Spotting/Filminq Data Powder Auto-Dish (3) 1st Cycle A 3 2nd Cycle A 3 3rd Cycle A 3,4 4th Cycle A 2,3 Powder ADD 11614-9OB (Chlorine Bleach) 1st Cycle : B5 2nd Cycle B5 3rd Cycle B5 4th Cycle B 3,4 Commercial Powder (Chlorine Bleach) 1st Cycle 2nd Cycle A 6 3rd Cycle A}3 6 4th Cycle A 3 Commerclal Liquid (Chlorine Bleach) 1st Cycle BC 3,4 2nd Cycle CD 4 3rd Cycle D 4,5 4th Cycle DE 2,3 Spotting Scale:
A best, no spots B very few spots C approx. 25~ spot coverage D approx. 50~ spot coverage E excessive coverage spots Filming Scale:
1 best, no film 2 slight film 3 noticeable film 4 significant fi.lm examine film 2~S~3 Example a~
According to the procedure of U.S. Patent 4,931,203 the followlng concentrated formulation was produced:
Table IX
Ingredients Concentration Sodium Tripolyphosphate Base Bead - DCP 151-627 61.00 Sodium Carbonate (Allied Chemical Dense Soda Ash) 10.00 Sodium Metasilicate ( 1 Na2O: 1 SiO2, PQ Metsobeads 2048~.00 Sodium Silicate (1 Na2O: 1 SiO2, PQ Britesil LD24) 12.00 Nonionic Surfactant (Union Carbide Tergitol MDS-42) 6.00 Maxatase P 440,000 (Gist Brocades) 3.50 Maxamyl P 5,000 (Gist Brocades) 1.50 The finished product is aged over two days to give a nice dry free-flowing powder.
Laboratory performance of the compositions of Example 2 were carried out using multi-soils. This was done to show differences between the prototype formulations and commercial products. Egg soil was prepared by mixing egg yolk with an equal amount of 2.5 N calcium chloride solution. This mixture was applied as thin cross-wise film to the usable surface of 7.5 inch china plates. The plates were aged in 50~ relative humidity overnight. Oatmeal soil was prepared by boiling 24 grams of Quaker Oats in 400 ml of tap water for ten minutes.
Three grams of this mixture was spread as thin film onto a 7.5 inch china plate. The plates were aged for 2 hours at 80C.
They were then stored overnight at room temperature. Two plates of each egg and oatmeal were used per wash. The plates were placed in the same positions in the dishwasher. Thirty-5 three grams of the detergent was used as a single dose per34 wash. All plates were scored by measuring the percent area cleaned. The multi-soil cleaning test results are reported below. The results tabulated in Table IX were average of at least 2 runs. Average results reflect the average performance results obtained in three different water conditions.
The product was tested with 33g dose using the ASTM
method D 3556-79 spotting and filming test method combined with denatured egg soiled (egg yolk denatured with 2.5 M CaCl2 solution) along with the 50g dose. Enzyme containing prototype powder ADD completely removed egg soil and of commercial powder product oatmeal, whereas, commercial Powder barely removed any of the egg and oatmeal soil.
Table X
Cleaning performance Enzyme vs~ non-Enzyme based product.
Product Dose %Cleaninq Denatured Eqq - Baked-on Oatmeal Commercial ADD Product (Example 2) 33g 100 100%
CASCADE Powder (Commercial powder) 50g 40%
IMPROVED PHOSPHATE-CONTAINING POWDER AUTOMATIC DISHWAS~IING
COMPOSITION WITH ENZ~MES
BACKGROUND OF THE INVENTION
It has been found to be very useful to have enzymes in dishwashing detergent compositions because enzymes are very effective in removing food soils from the surface of glasses, dishes, pots, pans and eating utensils. The enzymes attack these materials while other components of the detergent will effect other aspects of the cleaning action. However, in order for the enzymes to be highly effective, the composition must be chemically stable, and it must maintain an effective activity at the operating temperature of the automatic dishwasher. Chemical stability such as to bleach agents is the property whereby the detergent composition containing enzymes does not undergo any significant degradation during storage. Activity is the property of maintaining enzyme activity during usage. From the time that a detergent i9 packaged until it is used by the customer, it must remain stable. Furthermore, during customer usage of the dishwashing detergent, it must retain its activity. Unle,ss the enzymes in the detergent are maintained in a minimum exposure to moisture and water, the enzymes will suffer a degradation during storage which will result in a product that will have a decreased activity. When enzymes are a part of ~he detergent composition, it has been found that the initial water content of the components of the composition should be as low a lev~l 20fi~8~3 d9 possible, and this low water content must be maintained during storage, since water will in the alkaline product deactivate the enzymes. This deactivation will cause a decrease in the initial activity of the detergent composition.
After the detergent container is opened, the detergent will be exposed to the environment which contains moisture.
During each instance that the detergent is exposed to the environment it could possibly absorb some moisture. This absorption occurs by components of the detergent composition absorbing moisture, when in contact with the atmosphere. This effect is increased as the container is emptied, since there will be a greater volume of air in contact with the detergent, and thus more available moisture to be absorbed by the detergent composition. This will usually accelerate the decrease in the activity of the detergent composition. The most efficient way to keep a high activity is to start with an initi.al high activity of enzyme and to use components in the dishwashing composition which do not interact with the enzyme or which have a low water affinity which will minimize any losses in activity as the detergent is being stored or used.
Powdered detergent compositions which contain enzymes can be made more stable and to have a high activity, if the initial free water content of the detergent composition is less than 10 percent by weight, more preferably less than 9 percent by weight and most preferably less than 8 percent by weight. Furthermore, the pH of a 1.0 wt% aqueous solution of the powdered detergent composition should be less than 11.0 more preferably less than 10.6, and most preferably less than 10.3. This low alkalinity of the dishwashing detergent should 2~8~3 maintain the stability of the detergent compositlon which contains a mixture of enz~mes, thereby providing a higher initial activity of the mixture of the enzymes and the maintenance of this initial high activity. A major concern in the use of automatic dishwashing compositions is the formulation of automatic dishwashing compositions which have a low alkalinity and can operate at a high temperature while maintaining superior cleaning performance and dish care. The present invention teaches the preparation and use of powdered automatic dishwashing compositions which are phosphate-containing and have superior cleaning performance and dish care, and are used at operating temperatures of 100F to 140F.
SUMMARY OF THE INVENTION
This invention is directed to producing powdered phosphate, enzyme-containing automatic dishwashing detergent compositions that have an increased chemical stability and essentially a high activity at wash operating temperatures of 40C to 65C (104F to about 150F), wherein the composition also can be used as a laundry pre-soaking agent. This is accomplished by controlling the alkalinity of the detergent composition and using a unique mixture of enzymes. An alkali metal silicate i9 used in the powdered dishwashing detergent compositions. The preferred builder system of the instant compositions comprises at least one phosphate builder salt which can be used in conjunction with polymeric builder salts and non-phosphate containing builder salts.
It is to be understood that the term powder in this invention includes within its definition tablets, soluble 2~6~8~3 capsules and soluble sachet. It is also possible to use the instant compositions as a laundry presoaking powder.
Conventional powdered automatic dishwashing compositions usually contain a low foaming surface-active agent, a chlorine bleach, alkaline builder materials, and usually minor ingredients and additives. The incorporation of chlorine bleaches requires special processing and storage precautions to protect composition components which are subject to deterioration upon direct contact with the active chlorine.
The stability of the chlorine bleach is also critical and raises additional processing and storage difficulties. In addition, it is known that automatic dishwasher detergent compositions may tarnish silverware and damage metal trim on china as a result of the presence of a chlorine-containing bleach therein. Accordingly, there is a standing desire to formulate detergent compositions for use in automatic dishwashing operations which are free of active chlorine and which are capable of providing overall hard surface cleaning and appearance benefits comparable to or better than active chlorine-containing detergent compositions. This reformulation is particularly delicate in the context of automatic dishwashlng operations, since during those operations, the active chlorine prevents the formation and/or deposition of tr~ublesome protein and protein-grease complexes on the hard dish surfaces and no surfactant system currently known is capable of adequately performing that function.
Various attempts have been made to formulate bleach-free low foaming detergent compositions for automatic dishwashing machines, containing particular low foaming nonionics, 2~8~3 ~uilders, filler materials and enzymes. US Patent 3,472,783 to Smille recognized that degradation of the enzyme can occur, when an enzyme is added to a highly alkaline automatic dlshwashing detergent.
French Patent No. 2,102,851 to Colgate-Palmolive, pertains to rinsing and washing compositions for use in automatic dishwashers. The compositions disclosed have a pH of 6 to 7 and contain an amylolytic and, if desired, a proteolytic enzyme, which have been prepared in a special manner from animal pancreas and which exhibit a desirable activity at a pH
in the range of 6 to 7. German Patent No. 2,038,103 to Henkel ~ Co. relates to aqueous licluid or pasty cleaning compositions containing phosphate salts, enzymes and an enzyme stabilizing compound. US Patent No. 3,799,879 to Francke et al, teaches a detergent composition for cleaning dishes, with a pH of from 7 to 9 containing an amylolytic enzyme, and in addition, optionally a proteolytic enzyme.
US Patent 4,101,457, to Place et al., teaches the use of a proteolytic enzyme having a maximum activity at a pH of 12 in an automatic dishwashing detergent.
US Patent 4,162,987, to Maguire et al., teaches a granular or licIuid automatic: dishwashing detergent which uses a proteolytic enzyme having a maximum activity at a pH of 12 as well as an amylolytic enzyme having a maximum activity at a pH
of 8.
US Patent No 3,827,938, to Aunstrup et al., discloses specific proteolytic enzymes ~hich exhibit high enzymatic activities in highly alkaline systems. Similar disclosures are found in British Patent Specification No. 1,361,386, to 2QS~53 ~OVO Terapeutis~ Laboratorium A/S. British Patent Specification No. 1,296,839, to Novo Terapeutisk Laboratorium A/S, discloses specific amylolytic enzymes which exhibit a high degree of enzymatic activity in alkaline systems.
Thus, while the prior art clearly recognizes the disadvantages of using aggressive chlorine bleaches in automatic dishwashing operations and also suggests bleach-free compositions made by leaving out the bleach component, said art disclosures are silent about how to formulate an effective bleach-free powdered automatic dishwashing compositions capable of providing superior performance during conventional use .
US Patent Nos. 3,821,118 and 3,840,480; 4,568,476, 4,501,681 and 4,692,260 teach the use of enzymes in automatic dishwashing detergents, as well as Belgian Patent 895,459;
French Patents 2,544,393 and 1,600,256; European Patents 256,679; 266,904; 271,155; 139,329; and 135,226; and Great Britain Patent 2,186,884.
The aforementioned prior art fails to provide a stable powdered automatic dishwashing detergent which is phosphate-containing and contains a mixture of enzymes as well as optionally, a peroxygen compound with a.n activator for the simultaneous degradation of both proteins and starches, wherein the combination of anylase and protease enzymes have a maximum activity at a pH of less than 11.0 and the powdered automatic dishwashing detergent has high cleaning performance in a temperature range of 40C to 65C (104F to 150F). It is an object of this invention to incorporate a novel enzyme mixture in a phosphate-containing, powdered automatic 2~S~8~3 ~ishwasher detergent composition for use in automatlc dishwashing operations capable of providing at least equal or better performance to conventional automatic dishwashing compositions at operating temperatures of 100F to 150F.
DETAILED DESCRIPTION
The present invention relates to a powdered automatic dishwashing detergent compositions which comprise a nonionic surfactant, alkali metal silicate, a phosphate-containing builder system, optionally, a peroxygen compound with an activator as a bleaching agent and a mixture of an amylase enzyme and a protease enzyme, wherein the powdered automatic dishwashing detergent composition has a pH of less than 11.0 and the powdered dishwashing detergent composition exhibits high cleaning efficiency for both proteins and starches at a wash temperature of 40C to 65C (100F to 150F).
The nonionic surfactants that can be used in the present powdered automatic dishwasher detergent compositions are well known. A wide variety of these surfactants can be used.
The nonionic synthetic organic detergents are generally described as ethoxylated propoxylated fatty alcohols which are low-foaming surfacl:ants and may be possibly capped, characterized by the presence of an organic hydrophobic group and an organic hydrophilic group and are typically produced by the condensation of an organic aliphatic or alkyl aromatic hydrophobic compound with ethylene oxide and/or propyleneoxide (hydrophilic in nature). Practically any hydrophobic compound having a carboxy, hydroxy, amide or amino group with a free hydrogen attached to the oxygen or the nitrogen can be condensed with ethylene oxide or propylene oxide or with the 20~t~853 polyhydration product thereof, polyethylene glycol, to form a nonionic detergent. The length of the hydrophilic or polyoxyethylene chain can be readily adjusted to achieve the desired balance between the hydrophobic and hydrophilic groups. Typical suitable nonionic surfactants are those disclosed in US Patent Nos. 4,316,812 and 3,630,929.
Preferably, the nonionic detergents that are used are the low-foaming polyalkoxylated lipophiles wherein the desired hydrophile-lipophile balance is obtained from addition of a hydrophilic poly-lower alkoxy group to a lipophilic moiety. A
preferred class of the nonionic detergent employed is the poly-lower alkoxylated higher alkanol wherein the alkanol is of 9 to 18 carbon atoms and wherein the number of moles of lower alkylene oxide (of 2 or 3 carbon atoms) is from 3 to 15.
Of such materials it is preferred to employ those wherein the higher alkanol is a high fatty alcohol of 9 to 11 or 12 to 15 carbon atoms and which contain from 5 to 15 or 5 to 16 lower alkoxy groups per mole. Preferably, the lower alkoxy is ethoxy but in some instances, it may be desirably mixed with propoxy, the latter, if present, usually being ma~or (more than 50~) portion. Exemplary of such compounds are those wherein the alkanol i9 of 12 to 15 carbon atoms and which contaln about 7 ethylene oxide groups per mole.
Useful nonionics are represented by the low foam Plurafac series from BASF Chemical Company which are the reaction product of a higher linear alcohol and a mixture of ethylene and propylene oxides, containing a mixed chain of ethylene oxide and propylene oxide, terminated by a hydroxyl group.
~xamples include Product A(a C~3- Cls fatty alcohol condensed 2 ~3 6 ~ 8 r~ 3 ~ith 6 moles ethylene oxide and 3 moles propylene o~ide).
Product B (a 13-Cls fatty alcohol condensed with 7 mole propylene oxide and 4 mole ethylene oxide), and Product C (a C13- C15 fatty alcohol condensed with 5 moles propylene oxide and 10 moles ethylene oxide). Another group of liquid nonionics - are available from Shell Chemical Company, Inc. under the Dobanol t~ademark: Dobanol 91-5 is a low foam ethoxylated Cg-Cl1 fatty alcohol with an average of 5 moles e~hylene oxide and Dobanol 25-7 is an ethoxylated Cl2-Cl5 fatty alcohol with an average of 7 moles ethylene oxide. Another liquid nonionic surfactant that can be used is sold under the tradename Lutensol SC 9713.
Poly-Tergent nonionic surfactants from Olin Organic Chemicals such as Poly-Tergent SLF-18, a biodegradable, low-foaming surfactant is specially preferred for the powdered automatic dishwasher detergent compositions of this instant invention. Poly-Tergent SLF-la, a water dispersible having a low cloud point, has lower surface tension and lower foaming is very suitable for automatic dishwasher detergent.
Synperonic nonionic surfactants from ICI such as Synperonic LF/D25, LF/RA30 are especially preferred nonionic surfactants that can be used in the powdered automatic dishwasher detergent compositi.ons of the instant invention. Poly-Tergent nonionic surfactants from Olin Organic Chemicals such as Poly-Tergent SLF-18, a biodegradable, low-foaming surfactant is specially preferred for the powdered automatic dishwasher detergent compositions of this instant invention. Poly-Tergent SLF 18, a water dispersible, having a low cloud point nas lower surface tension and lower foaming is very sultable for automatic dishwasher detergent Other useful surfactan~s are Neodol 25-7 and Neodol 23-6.5, which products are made by Shell Chemical Company, Inc.
The former is a condensation product of a mixture of higher fatty alcohols averaging about 12 to 13 carbon atoms and the number of ethylene oxide groups present averages 6.5. The hlgher alcohols are primary alkanols. Other examples of such detergents lnclude Tergitol 15-S-7 and Tergitol 15-S-9 (registered trademarks), both of which are linear secondary alcohol ethoxylates made by Union Carbide Corp. The former is mixed ethoxylation product of 11 to 15 carbon atoms linear secondary alkanol with seven moles of ethylene oxide and the latter i9 a similar product but with nine moles of ethylene oxide being reacted.
Also useful in the present compositions as a component of the nonionic detergent are higher molecular weight nonionics, such as Neodol 45-11, which are similar ethylene oxide condensation products of higher fatty alcohols, with the higher fatty alcohol being of 14 to 15 carbon atoms and the number of ethylene oxide groups per mole being 11. Such products are also made by Shell Chemical Company.
In the preferred poly-lower alkoxylated higher alkanols, to obtain the best balance of hydrophilic and lipophilic moieties the number of lower alkoxies will usually be from 40%
to 100% of the number of carbon atoms in the higher alcohol, preferably 40 to 60% thereof and the nonionic detergent will preferably contain at least 50% of such preferred poly-lower alkoxy higher alkanol.
The alkyl polysaccharides are surfactants which are also useful alone or in conjunction with the aforementioned surfactants and those having a hydrophobic group containing from 8 to 20 carbon atoms, preferably from 10 to 16 carbon atoms, most preferably from 12 to 14 carbon atoms, and polysaccharide hydrophilic group containing from 1.5 to 10, preferably from 1.5 to 4, and most preferably from 1.6 to 2.7 saccharide units (e.g., galactoside, glucoside, fructoside, glucosyl, fructosyl, and/or galactosyl units). Mixtures of saccharide moieties may be used in the alkyl polysaccharide surfactants. The number x indicates the number of saccharide units shown later in a particular alkyl polysaccharide surfactant formula. For a particular alkyl polysaccharide molecule x can only assume integral values. In any physical sample can be characterized by the average value of x and this average value can assume non-integral values. In this specification the values of x are to be understood to be average values. The hydrophobic group (R) can be attached at the 2-, 3-, or 4- positions rather than at the l-position, (thus giving e.g. a glucosyl or galactosyl as opposed to a glucoside or galactoside). However, attachment through the 1-position, i.e., glucosides, galactosides, fructosides, etc., i9 preferred. In the preferred product the additional saccharide units are predominately attached to the previous saccharide unit's 2-position. Attachment through the 3-, 4-, and 6-positions can also occur. Optionally and less desirably there can be a polyalkoxide chain joining the hydrophobic moiety (R) and the polysaccharide chain. The preferred alkoxide moiety is ethoxide.
2 ~ 3 Typical hydrophobic groups include alkyl groups, either ~ saturated or unsaturated, branched or unbranched containing - from 8 to 20, preferab]y from 10 to 16 carbon atoms.
Preferably, the alkyl group is a straight chain saturated alkyl group. The alkyl group can contain up to 3 hydroxy groups and/or the polyalkoxide chain can contain up to about 30, preferably less than 10, alkoxide moieties.
Suitable alkyl polysaccharides are decyl, dodecyl, tetradecyl, pentadecyl, hexadecyl, and octadecyl, di-, tri-, tetra-, penta-, and hexaglucosides, galactosides, lactosides, fructosides, fructosyls, lactosyls, glucosyls and/or galactosyls and mixtures thereof.
The alkyl monosaccharides are relatively less soluble in water than the higher alkyl polysaccharides. When used in admixture with alkyl polysaccharides, the alkyl monosaccharides are solubilized to some extent. The use of alkyl monosaccharides in admixture with alkyl polysaccharides is a preferred mode of carrying out the invention. Suitable mixtures include coconut alkyl, di-, tri-, tetra-, and pentaglucosides and tallow alkyl tetra-, penta-, and hexaglucosides.
The preferred alkyl polysaccharides are alkyl polyglucosides having the formula:
R2O(CnH2nO)r(z)~
wherein Z is derived from glucose, R i9 a hydrophobic group selected from the group consisting of alkyl, alkylphenyl, hydroxyalkylphenyl, and mixtures thereof in which said alkyl groups contain from 10 to 18, preferably from 12 to 14 carbon atoms; n is 2 or 3 preferably 2, r is from 0 to 10, preferable 2Q$~3 0; and x is from 1.5 to 8, preferably from 1 5 to ~, most preferably from 1.6 to 2.7. To prepare these compounds a long chain alcohol (R2OH) can be reacted with glucose, in the presence of an acid catalyst to form the desired glucoside.
Alternatively the alkyl polyglucosides can be prepared by a two step procedure in which a short chain alcohol (RIOH) an be reacted with glucose, in the presence of an acid catalyst to form the desired glucoside. Alternatively the alkyl polyglucosides can be prepared by a two step procedure in which a short chain alcohol (Cl6) is reacted with glucose or a polyglucoside (x=2 to 4) to yield a short chain alkyl glucoside (x=1 to 4) which can in turn be reacted with a longer chain alcohol (R2OH) to displace the short chain alcohol and obtain the desired alkyl polyglucoside. If this two step procedure is used, the short chain alkylglucoside content of the final alkyl polyglucoside material should be less than 50~, preferably less than 10~, more preferably less than 5~, most preferably 0% of the alkyl polyglucoside.
The amount of unreacted alcohol (the free fatty alcohol content) in the desired alkyl polysaccharide surfactant is preferably less than 2~, more preferably less than 0.5% by weight of the total of the alkyl polysaccharide. For some uses it is desirable to have the alkyl monosaccharide content less than about 10~.
The used herein, "alkyl polysaccharide surfactant" is intended to represent both the preferred glucose and galactose derived surfactants and the less preferred alkyl polysaccharide surfactants. Throughout this specification, "alkyl polyglucoside" is used ~o include alkyl polyglycosides 2 ~ 3 oecause the stereo chemistry of the saccharide moiety is changed during the preparation reaction.
An especially preferred APG glycoside surfactant is APG
625 glycoside manufactured by the E~enkel Corporation of Ambler, PA. APG 625 is a nonionic alkyl polyglycoside characterized by the formula:
CnH2n+,0 (C6HI005) lH
wherein n=10(2~); n=12(65~); n=14(21-28%); n=16(4-8~) and n=18(0.5~) and x(degree of polymerization) = 1.6. APG 625 has: a pH of 6-~(10~ of APG 625 in distilled water); a specific gravity at 25F of 1.1 grams/ml; a density at 25F of 9.1 kgs/gallons; a calculated HLB of 12.1 and a Brookfield viscosity at 35C, 21 spindle, 5-10 RPM of 3,000 to 7,000 cps.
Mixtures of two or more of the liquid nonionic surfactants can be used and in some cases advantages can be obtained by the use of such mixtures.
The liquid nonaqueous nonionic surfactant is absorbed on a builder system which comprises a phosphate-containing particles which is a builder salt and optionally a low 2~ molecular weight polyacrylate type polymer such as a polyacrylate organic and/or inorganic detergent builders as well as phosphate-free builder salts such as an alkali carbonate such as sodium carbonate or sodium citrate or a mixture of sodium carbonate and sodium citrate. A preferred solid builder salt is an alkali metal polyphosphate such as sodium tripolyphosphate ("TPP"). The TPP is a blend of anhydrous TPP and a small amount of TPP hexahydrate such that the chemically bound water content is 1~, which corresponds to about one H20 per pentasodium tripolyphosphate molecule. Such g ~ 3 ~P may be produced by treating anhydrous TPP with a limited amount of water. The presence of the hexahydrate slows down the rapid rate of solution of the TPP in the wash bath and inhibits caking. One suitable TPP is sold under the name Thermphos NW. The particles size of the Thermphos NW TPP, as supplied, usually averages about 200 microns with largest particles being about 400 microns. In place of all or part of the alkali metal polyphosphate one or more other detergent builder salts can be used. Suitable other builder salts are alkali metal carbonates, borates, phosphates, bicarbonates, silicates, lower polycarboxylic acid salts, and polyacrylates, polymaleic anhydrides and copolymers of polyacrylates and polymaleic anhydrides and polyacetal carboxylates.
Specific examples of such builders are sodium carbonate, potassium carbonate, sodium tetraborate, sodium pyrophosphate, sodium bicarbonate, sodium hexametaphosphae, sodium sesquicarbonate, sodium mono and diorthophosphate, and potassium bicarbonate. The builder salts can be used alone with the nonionic surfactant or in an admixture with other builders. Typical builders also include those disclosed in U.S. Pat Nos. 4,316,812, 4,264,466 and 3,630,929 and those disclosed in U.S. Pat Nos. 4,144,226, 4,135,092 and 4,146,495, all of which are herein incorporated by reference.
Other phosphate-free builder salts which can be mixed with the phosphate containing builder salts are gluconates, phosphonates, and nitriloacetic acid salts in conjunction with the builder salts are optionally used a low molecular weight polyacrylates having a molecular weight of 1,000 to 100,000, more preferably about 2,000 to about 80,000. A preferred low 2~8~3 ~.olecular weiyht polyacrylate is Sokalan~nCP45 or Sokalan~CP5 manufactured by BASF and having a molecular weight of 70,000.
Another preferred low molecular weight polyacrylate is Acrysol~LMW45ND manufactured by Rohm and Haas and having a molecular weight of 4,500. NorasolTMWL2 comprises 26~ LMW45ND
sprayed on 74~ soda ash.
Sokalan~CP45 or CP5 is a copolymer of an acrylic acid and maleic acid anhydride. Such a material should have a water absorption at 38C and 78 percent relative humidity of less than about 40 percent and preferably less than 30 percent.
The builder is commercially available under the tradename of Sokalan~CP45. This is a partially neutralized copolymer of acrylic acid and maleic anhydride sodium salt. Sokalan~CP5 is classified as a suspending and anti-deposition agent. This suspending agent has a low hygroscopicity. Another builder salt is Sokalan~MCP5 having a molecular weight of 70,000 which is a completely neutralized version of CP45. An ob~ective i9 to use suspending and anti-redeposition agents that have a low hygroscopicity. Copolymerized polyacids have this property, and particularly when partially neutralized. ~cusol~'64ND
provided by Rohm Haas is another useful suspending agent.
Another class of builders useful herein are the aluminosilicates, both of the crystalline and amorphous type.
Various crystalline zeolites (i.e. alumino-silicates) are described in British Patent No. 1,504,168, U.S. Patent No.
4,409,136 and Canadian Patent Nos. 1,072,835 and 1,087,477.
An example of amorphous zeolites useful herein can be found in Belgium Patent No. 835,351. The zeolites generally have the formula 20~53 (M2O)~(Al~O3)y(SiO2)x wH2O
wherein x is 1, y is from 0.8 to 1.2 and preferably 1, z is from 1.5 to 3.5 or higher and preferably 2 to 3 and w is from 0 to 9, preferably 2.5 to 6 and M is preferably sodium. A
typical zeolite is type A or similar structure, with type 4A
particularly preferred. The preferred aluminosilicates have calcium ion exchange capacities of 200 milliequivalents per gram or greater, e.g. 400 meq/g.
The alkali metal silicates are useful anti-corrosion agents which function to make the composition anti-corrosive to eating utensils and to automatic dishwashing machine parts.
Sodium silicates of Na2O:SiO2 ratios of from 1:1 to 1:2.4.
Potassium silicates of the same ratios can also be used. The preferred silicates are sodium disilicate and sodium metasilicate.
Essentially, any compatible anti-foaming agent can be used. Preferred anti-foaming agents are silicone anti-foaming agents. The~e are alkylated polysiloxanes and include polydimethyl siloxanes, polydiethyl siloxanes, polydibutyl siloxanes, phenyl methyl siloxanes, trimethysilanated silica and triethylsilanated silica. A suitable anti-foaming agent is Silicone TP-201 from Union Carbide. Other suitable anti-foaming agents are Silicone DB700, DB100 used at 0.2 to 1.0 percent by weight, sodium stearate used at a concentration level of 0.5 to 1.0 weight percent and 1.0 weight percent, and LPKn 158 (phosphoric ester) sold by Hoechst used at a concentration level of 0 to 1.5 weight percent, more preferably 0.1 to 1.0 weight percent. The perfumes that can be used include lemon perfume and other natural scents.
2~8~3 _ssentially, any opacifier that is compatible with the remaining components of the detergent formulation can be used.
A useful and preferred opacifier is titanium dioxide at a concentration level of 0 to 1.0 weight percent.
A key aspect is to keep the free water (non-chemically bounded water) in the detergent composition at a minimum.
Absorbed and adsorbed water are two types of free water, and comprise the usual free water found in a detergent composition. Free water will have the affect of deactivating the enzymes.
The detergent composition of the present invention can include a peroxygen bleaching agent at a concentration level of 0 to 20 weight percent, more preferably 0.5 to 17 weight percent and most preferably at 1.0 to 14 weight percent. The oxygen bleaching agents that can be used are alkali metal perborates, percarbonate, perphthalic acid, perphosphates, and potassium monopersulfate. A preferred compound is sodium perborate monohydrate and dihydrate. The peroxygen bleaching compound is preferably used in admixture with an activator thereof at a concentration level of 1 to about 5 weight percent. Suitable activators are those disclosed in U.S.
Patent No. 4,264,466 or in column 1 of U.S. Patent No.
4,430,244. Polyacetylated compounds are preferred activators.
Suitable preferred activators are tetraacetyl ethylene diamine ("TAED"), pentaacetyl glucose and ethylidenebenzoate acitate.
The activator usually interacts with the peroxygen compound to form a peroxyacid bleaching agent in the wash water.
2~6$8~3 The detergent formulation also contains a mixture of a protease enzyme and an amylase enzyme and, optionally, a lipase enzyme that serve to attack and remove organic residues on glasses, plates, pots, pans and eating utensils. Lipolytic enzymes can also be used in the powdered automatic dishwasher detergent composition. Proteolytic enzymes attack protein residues, lipolytic enzymes fat residues and amylolytic enzymes starches. Proteolytic enzymes include the protease enzymes subtilisn, bromelin, papain, trypsin and pepsin.
Amylolytic enzymes include amylase enzymes. Lipolytic enzymes include the lipase enzymes. The preferred amylase enzyme is available under the name Maxamyl, derived from Bacillus licheniformis and is available from Gist-brocades of the Netherlands in the form of a prill having an activity of about 5,000 TAU/g. One of the preferred protease enzyme is available under the name Maxapem 15, 20, 30 or Maxapem 42 which is a high alkaline mutant proteolytic enzyme derived from Bacillus acalophylus, and is available from Gist-Brocades, of the Netherlands in a prill form (activity of about 15, 20, 30 or 40 MPU/g). Preferred enzyme activates per wash are Maxapem 10-100 MPU/g per wash and Maxamyl 625 to 4,000 TAU/g per wash. Another preferred protease enzyme is available under the name Maxatase derived from a novel Bacillus strain designated "PB92" wherein a culture of the Bacillus is deposited with the laboratory for Microblology of the Technical University of Delft and has a number R-60, and ls available from Gist-Brocades, of the Netherlands in prill form (activity of about 440 KDU/g). Preferred enzyme activates per wash are Maxatase 200-700 KDU/g per wash.
2~98~3 The weight ratio of the proteolytic enzyme to the amylolytic en~yme in the powdered automatlc dishwasher detergent compositions is 8:1 to 1:1, and more preferably 4.5:1 to l.1:1.
The detergent composition can have a fairly wide ranging composition. The surfactant can comprise 0 to 15 percent by weight of the composition, more preferably 0.1 to 15 percent by weight, and most preferably 1 to 12 percent by weight. The soil suspending agent which is preferably a copolymerized polyacrylic acid will be present in an amount of 0 to 20 percent by weight, more preferably 3 to 15 percent by weight and most preferably 5 to 15.0 percent by weight. The anti-foaming agent will be present in an amount of 0 to 1.5 percent by weight, more preferably 0.1 to 1.2 percent by weight and most preferably 0.3 to 1 percent by weight. The builder system, which is preferably an alkali metal tripolyphosphate and/or an alkali metal pyrophosphate, is present in an amount of 2 to 40 percent by weight, more preferably about 4 to about 40 percent by weight and most preferably 5 to 35 percent by weight for a standard product. However, for a concentrated formula, the alkali metal tripolyphosphate is present in an amount of 10 to 65 weight percent, more preferably 15 to 65 by weight, and most preferably 15 to 62~ by weight percent.
The builder system can also contain a low molecular weight polyacrylate type polymer at a concentration level of 0 to 20 w~ight percent, more preferably 1.0 to 17 weight percent and most preferably about 2 to 14 w~ight percent.
The alkali silicate, which is a corrosion inhibitor, wherein sodium disilicate is preferred, will be present in an 2~.9~3 ~ mount of 0 to 30 percent by weight, more preferably 3 to 30 percent by weight and most preferably 4 to 28 percent by weight.
The opacifier will be present in an amount of 0 to 1.0 percent by weight, more preferably about 0.1 to 7 percent by weight and most preferably 0.4 percent by weight.
The enzymes will be present in a prilled form as supplied by Gist Brocades at a concentration of 0.8 to 22.0 percent by weight, more preferably 0.9 to 20.0 percent by weight, and most preferably 1.0 to about 18.0 percent by weight. The protease enzyme prills in the automatic dishwashing composition will about 0.5 to 15.00 percent by weight, more preferably 0.7 to 13.0 weight percent and most preferably 0.8 to 11.0 percent by weight. The amylase enzyme prills will comprise 0.3 to 8.0 percent by weight, more preferably 0.4 percent to 7.0 weight percent and most preferably 0.5 to 6.0 weight percent. The lipase enzyme prills will comprise 0.00 to 8.0 percent by weight of the detergent composition. A
typical lipase enzyme is Lipolas 100 T from NOVO Nordisk of Denmark. The lipase enzymes are especially beneficial in reducing grease residues and related filming problems on glasses arld dishware. Another useful lipase enzyme is Amaneo PS lipase provided by Amaneo International Enzyme Co., Inc.
Other components such as perfumes will comprise about 0.1 to about 5.0 percent by weight of the detergent composition.
One method of producing the detergent powder formulation consisting first of spraying and absorbing nonionic surfactant into the phosphate and carbonate builder salts and mixed thoroughly in a rotary drum. The absorbed builder salt was ~Q~53 hen aged overnight to completely absorb the nonionic to form a free flowing powder which was then mixed with sodium sulfate and silicate in a twin-shelled blender. Finally, enzyme prills were added and mixed thoroughly to form a free flowing detergent powder. Another method of producing the powder detergent forl~ulation having a bulk density of 0.9 is to spray dry by any conventional means the nonionic surfactant and defoamer into the perborate bleach compound and the builder salt. This spray dry materials can be used immediately, but it is preferred to age then for 24 hours. The spray dried materials are dry blended in any suitable conventional blender such as a tumble blender at about room temperature with the other ingredients of the composition until a homogenous blend is obtained.
The instant compositions also can be produced as low density powders according to the procedure as set forth in U.S. Patent 4,931,203, wherein these powders have a bulk density 1/3 less than the bulk density of the bulk density of the standard powders which have a bulk density of 1.0 kg/liter.
The concentrated powdered nonionic automatic dishwashing detergent compositions of the present invention disperses readily in the water in the dishwashing machine. The presently used home dishwashing machines have a measured capacity for 80cc or 90 grams of detergent. In normal use, for example, for a full load of dirty dishes 60 grams of powdered detergent are normally used.
In accordance with the present invention only about 56cc or about 50 grams of the standard powdered detergent 2QS~3 omposition is needed whereas the dose of concentrated detergent is 33 g weight. The normal operation of an automatic ~ishwashing machine can involve the following steps or cycles: washing, rinse cycles with cold/hot water and rinse cycles with hot water. The entire wash and rinse cycles require 60 minutes. The temperature of the wash water is 40C
to 65C and the temperature of the rinse water is 55C to 65C. The wash and rinse cycles use about 4 to 7.5 liters of water for the wash cycle and about 4 to 7.5 liters of water for the hot rinse cycle.
The concentrated powdered automatic dishwashing detergent compositions exhibit excellent cleaning properties and because of the high concentration of the detergent in the composition, the detergent is not totally consumed during the wash cycle or totally eliminated during the rinse cycle such that there i9 a sufficient amount of detergent remaining during the rinse cycle to substantially improve the rinsing. The washed and dried dishes are free of undesirable traces, deposits or film due to the use of hard water in the rinse cycle.
DESCRIPTION OF THE PREFERRED EMBODIMENTS
Example 1 Standard Density Powder Auto-Dish Detergent Composition A free flowing, highly soluble standard density powder auto-dish detergent was developed by absorbing nonionic surfactant (Union Carbide Tergitol MDS-42) on highly absorptive sodium tripolyphosphate (Oxy Chem HRS3342). High 2~6~8~
,oluble sodium silicate (PQ Corporation ~IS 240), granular sodium sulfate (Kerr-McGee Corporation Trona), granular sodium carbonate (Allied Chemical dense soda ash) were also necessary to give necessary flow property and high solubility of the 5 detergent. Product was made by dry blending all the ingredients.
Table I
Ingredi~ Amount Concentration Sodium Tripolyphosphate (Oxychem HRS3342) 144g 36%
Anhydrous Sodium Sulfate-Trona Gran. 104 26 Anhydrous Sodium Carbonate-Allied Dense 88 Hydrated Sodium Silicate - PQ HS 240 48 12 Nonionic Surfactant - Tergitol MDS-42 16 Maxapem CX 30 MPU- Gist-Brocades 0 Maxamyl P 5000 - Gist-Brocades 0 400g 100%
Amount of Maxapem 30 and Maxamyl enzymes were incorporated in the powder ADD general formula as exemplified in Table I by replacing equivalent amount of sodium sulfate in the product.
Rest of the ingredients and the amount remained same in the product.
The finished product was aged over a period of two days to give a nice dry free-flowing powder. The product was tested with 50g dose using the ASTM spotting and filming teRt method combined with denatured egg soiled (egg yolk denatured with 2.5 M CaCl2 solution) along with haked-on oatmeal soiled substrates against non-enzyme powder ADD, bleach-containing powder ADD prototype and CASCADE, a commercial powder ADD with 50g dose and PALMOLIVE AUTOMATIC, a commercial 2 ~ 3 ~iquid ADD with 80g dose. Tne cleaning performance tests were run at 120F wash cycle temperatures using tap water (ca. 115 ppm water hardness).
2 0 ~ 3 Table II
Auto-Dish Performance (Enzyme V9. Non-Enzyme vs. Bleach-Based Product) In Tap Water at 120F Wash Cycle Temperature Auto-Dish Enzyme _Conc. %Dose g Performance, Cleaning Products Maxapem 30 Maxamyl Denatured Egg Baked-On Porridge 1 0 0 50g 6.5% 60.0 2 0 1 50g 30.5 99.5 3 2 0 50g 98.0 60.0 4 2 1.5 50g 99.0 99.5 2 0.5 50g 95.0 98.5 6 1.5 0.25 50g 94.0 95.5 7 1 0.5 50g 93.0 100.0 8 1 0.25 50g 94.5 100.0 9 1 0.25 50g 68.5 100.0 PADD 11614-9OB (contain 1.2~ Av.C1) 50g 91.5 60.0~
CASCADE Powder (contain 1% Av.Cl) 50g 63.0 25 60.0~
PALM AUTO Liq (contain 1~ Av.Cl) 80g 91.0 60.0~
Non-enzyme poser ADD Conrol (1) barely cleaned any egg and starch soil whereas incorporation of Protein Engineered 42 Maxacal and Maxamyl helped complete removal egg and starchy soil respectively. Enzymes (both Maxapem 30 and Maxamyl) containing powders (2-9) outperformed chlorine bleach containing ADDs like PADD 11614-9OB, CASCADE, a commercial powder and PALMOLIVE AUTOMATIC, a commercial Liquid in cleaning egg and starchy soil.
2 ~ 3 Table III
Auto-Dish Products ASTM Spotting/Filming Performance Data 300 ppm Water Hardness, 120F Wash Cycle Temperature Auto-Dish Products Spotting/Filming Powder Auto-Dish (3) 1st Cycle A 3 2nd Cycle A 3 3rd Cycle A 3,4 4th Cycle A 2,3 Powder ADD 11614-9OB (Chlorine Bleach) 1st Cycle 2nd Cycle B5 3rd Cycle B5 4th Cycle B 3,4 CASCADE Powder (Chlorine Bleach) 1st Cycle A 5 2nd Cycle A 6 3rd Cycle AB 6 4th Cycle A 3 PALMOLIVE AUTOMATIC Liquid (Chlorine Bleach) 1st Cycle BC 3,4 2nd Cycle CD 4 3rd Cycle D ~,5 4th Cycle DE 2,3 Spotting Scale:
A best- no spots B very few spots C approximately 25~ spot coverage D approximately 50~ spot coverage E excessive spots Filming Scale:
1 best - no film 2 slight film 3 noticeable film 4 significant film excessive film 4~
2 0 ~ 3 Rxample 2 According to the procedure of U.S. Patent 4,931,203 the following concentrated formulation was produced:
Table I~
Inqredients Concentration Sodium Tripolyphosphate Base Bead - D CP 151-627 Protein Sodium Carbonate (Allied Chemical Dense Soda Ash) 10.00 Sodium Metasilicate ( 1 Na2O: 1 SiO2, PQ Metsobeads 2048~.00 Sodium Silicate (1 Na2O: 1 SiO2, PQ Britesil LD24) 12.00 Nonionic Surfactant (Union Carbide Tergitol MDS-42) 6.00 Maxapem CX 30 (Gist-Brocades) 1.50 Maxamyl P 5,000 (Gist-Brocades) The finished product is aged over two days to give a nice dry free-flowing powder.
Laboratory performance of the compositions of ~xample 2 were carried out using multi-soils. This was done to show differences between the prototype formulations and commercial products. Egg soil was prepared by mixing egg yolk with an equal amount of 2.5 N calcium chloride solution. This mixture was applied as thin cross-wise film to the usable surface of 7.5 inch china plates. The plates were aged in 50~ relative humidity overnight. Oatmeal soil was prepared by boiling 24 grams of Quaker Oats in 400 ml of tap water for ten minutes.
Three grams of this mixture was spread as thin film onto a 7.5 inch china plate. The plates were aged for 2 hours at 80C.
They were then stored overnight at room temperature. Two plates of each egg and oatmeal were used per wash. The plates 2~8.~3 were placed in the same positions in the dishwasher. Thirty-three grams of the detergent was used as a single dose per wash. All plates were scored by measuring the percent area cleaned. The multi-soil cleaning test results are reported below. The results tabulated in Table V were average of at least 2 runs. Average results reflect the average performance results obtained in three different water conditions. The product was tested with 33g dose using the ASTM Method D3556-79 spotting and filming test method combined with denatured egg soiled (egg yolk denatured with 2.5 M CaCl2 solution) along with the 50g dose of commercial powder product. Enzyme containing prototype powder ADD completely removed egg soil and major portion of oatmeal, whereas, CASCADE, a commercial powder barely removed any of the egg and oatmeal soil.
Table V
Cleaning performance, Enzyme v9. non-Enzyme Based Product Product Dose ~Cleaninq Denatured Eqq Baked-On Oatmeal Conc. ADD Product (Example 2) 33g 100~ 100 CASCADE Powder (Commercial Product) 50g 40~ 50 2~8~3 Example 3 Standard Density Powder Auto-Dish Detergent Composition A free flowing, highly soluble standard density powder auto-dish detergent was developed by absorbing nonionic surfactant (Union Carbide Tergitol MDS-42) on highly absorptive sodium tripolyphosphate (Oxy Chem HRS3342). High soluble sodium silicate (PQ Corporation HS 240), granular sodium sulfate (~err-McGee Corporation Trona), granular sodium carbonate (Allied Chemical dense soda ash) were also necessary to give necessary flow property and high solubility of the detergent. Product was made by dry blending all the ingredients.
Table VI
Inqredients Amount Concentration Sodium Tripolyphosphate (Oxy Chem HRS3342) 144g36 Anhydrous Sodium Sulfate-Trona Gran. 10426 Anhydrous Sodium Carbonate-Allied Dense 8822 Hydrated Sodium Silicate - PQ HS 240 4312 Nonionic Surfactant - Tergitol MDS-42 16 4 Maxatase - Gist Brocades O O
Maxamyl P 5000 - Gist-Brocades 0 400g 100~
Amount of Maxatase P440,000 and Maxamyl P5,000 prilled enzymes were incorporated in the powder ADD general formula as exemplified in Table VI by replacing equivalent amount of sodium sulfate in the product. Rest of the ingredients and the amount remained same in the product.
The finished product was aged over a period of two days to give a nice dry free-flowing powder. The product was tested with 50g dose using the ASTM spotting and filming test method combined 2~853 .~ith denatured egg soiled (egg yolk denatured with 2.5 M CaClz solution) along with baked-on oatmeal soiled substrates against non-enzyme powder ADD, bleach-containing powder ADD prototype and a commercial (CASCADE) powder ADD with 50g dose and a commercial (PALMOLIVE AUTOMATIC) Liquid ADD with 80g dose. The cleaning performance tests were run at 120F wash cycle temperatures using tap water (ca. 115 ppm water hardness).
2~S~3 Table VII
Auto-Dish Performance (Enzyme vs. Non-Enzyme vs. Bleach-Based Product) In Tap Water at 120F Wash Cycle Temperature Auto-Dish Enzymes Conc. ~ Dose g Performance, ~ Cleaning Products Maxatase Maxamyl Denatured Egg Baked-On Porridge 1 0 0 50g 7.5 60.0 2 0 1 50g32.0 99.0 3 2 0 50g95.0 60.0 4 2 1.5 50g98.5 99.5 2 0.5 50g95.0 98.5 6 1.50.25 50g96.0 96.0 7 1 0.5 50g96.0 100.0 8 1 0.25 50g95.0 100.0 9 1 0.25 50g70.5 100.0 Powder ADD
11614-9OB (contain 1.2~ Av.Cl)50g 91.5 60.0 Commercial Powder (contain 1~ Av.Cl) 50g63.0 60.0 Commercial Liq (contain 1~ Av.Cl) 80g91.0 60.0 Non-enæyme poser ADD Conrol (1) barely cleaned any egg and starch soil whereas incorporation of Maxatase and Maxamyl helped complete removal egg and starchy soil respectively.
Enzymes (both Maxatase and Maxamyl) containing powders (2-9) outperformed chlorine bleach containing ADDs like PADD 11614-90B, commercial powder and commercial Liquid in cleaning egg and starchy soil.
2 ~
Table VIII
: Auto-Dish Products ASTM Spotting~Filming Performance Data 300 ppm Water Hardness, 120F Wash Cycle Temperature Auto-Dish Products Spotting/Filminq Data Powder Auto-Dish (3) 1st Cycle A 3 2nd Cycle A 3 3rd Cycle A 3,4 4th Cycle A 2,3 Powder ADD 11614-9OB (Chlorine Bleach) 1st Cycle : B5 2nd Cycle B5 3rd Cycle B5 4th Cycle B 3,4 Commercial Powder (Chlorine Bleach) 1st Cycle 2nd Cycle A 6 3rd Cycle A}3 6 4th Cycle A 3 Commerclal Liquid (Chlorine Bleach) 1st Cycle BC 3,4 2nd Cycle CD 4 3rd Cycle D 4,5 4th Cycle DE 2,3 Spotting Scale:
A best, no spots B very few spots C approx. 25~ spot coverage D approx. 50~ spot coverage E excessive coverage spots Filming Scale:
1 best, no film 2 slight film 3 noticeable film 4 significant fi.lm examine film 2~S~3 Example a~
According to the procedure of U.S. Patent 4,931,203 the followlng concentrated formulation was produced:
Table IX
Ingredients Concentration Sodium Tripolyphosphate Base Bead - DCP 151-627 61.00 Sodium Carbonate (Allied Chemical Dense Soda Ash) 10.00 Sodium Metasilicate ( 1 Na2O: 1 SiO2, PQ Metsobeads 2048~.00 Sodium Silicate (1 Na2O: 1 SiO2, PQ Britesil LD24) 12.00 Nonionic Surfactant (Union Carbide Tergitol MDS-42) 6.00 Maxatase P 440,000 (Gist Brocades) 3.50 Maxamyl P 5,000 (Gist Brocades) 1.50 The finished product is aged over two days to give a nice dry free-flowing powder.
Laboratory performance of the compositions of Example 2 were carried out using multi-soils. This was done to show differences between the prototype formulations and commercial products. Egg soil was prepared by mixing egg yolk with an equal amount of 2.5 N calcium chloride solution. This mixture was applied as thin cross-wise film to the usable surface of 7.5 inch china plates. The plates were aged in 50~ relative humidity overnight. Oatmeal soil was prepared by boiling 24 grams of Quaker Oats in 400 ml of tap water for ten minutes.
Three grams of this mixture was spread as thin film onto a 7.5 inch china plate. The plates were aged for 2 hours at 80C.
They were then stored overnight at room temperature. Two plates of each egg and oatmeal were used per wash. The plates were placed in the same positions in the dishwasher. Thirty-5 three grams of the detergent was used as a single dose per34 wash. All plates were scored by measuring the percent area cleaned. The multi-soil cleaning test results are reported below. The results tabulated in Table IX were average of at least 2 runs. Average results reflect the average performance results obtained in three different water conditions.
The product was tested with 33g dose using the ASTM
method D 3556-79 spotting and filming test method combined with denatured egg soiled (egg yolk denatured with 2.5 M CaCl2 solution) along with the 50g dose. Enzyme containing prototype powder ADD completely removed egg soil and of commercial powder product oatmeal, whereas, commercial Powder barely removed any of the egg and oatmeal soil.
Table X
Cleaning performance Enzyme vs~ non-Enzyme based product.
Product Dose %Cleaninq Denatured Eqq - Baked-on Oatmeal Commercial ADD Product (Example 2) 33g 100 100%
CASCADE Powder (Commercial powder) 50g 40%
Claims (13)
1. A powdered detergent containing a mixture of a protease enzyme and an amylase enzyme which comprises 10 to 40 percent by weight of an alkali metal silicate wherein said dishwashing composition has a pH of less than 11Ø
2. The powdered dishwashing composition according to claim 1 wherein said dishwashing composition contains 0.5 to 13.0 percent by weight of said protease enzyme and 0.3 to 8.0 weight percent of said amylase enzyme.
3. The powdered dishwashing composition according to claim 2 wherein said dishwashing composition further contains a lipase enzyme.
4. The concentrated powdered dishwashing composition according to claim 1 wherein said dishwashing composition includes 2.0 to 15.0 percent by weight of said nonionic surfactant.
5. The powdered dishwashing composition according to claim 1 which comprises an effective amount of one or more adjuvants selected from the group consisting of anti-encrustation agents, oxygen bleaching agents, sequestering agents, anti-corrosion agents, anti-foam agents, opacifiers and perfumes.
6. The powdered dishwashing composition according to claim 1 which includes 0 to 20.0 percent by weight of a copolymerized polyacrylic acid and a copolymer thereof.
7. The concentrated powdered dishwashing composition according to claim 6 which contains an alkali metal perborate.
8. The concentrated powdered dishwashing composition according to claim 7 which contains an alkali metal perborate activator.
9. The concentrated powdered dishwashing composition according to claim 5 which contains a lipase enzyme.
10. The concentrated powdered dishwashing composition according to claim 2 wherein said dishwashing composition comprises in percent by weight:
low molecular weight polyacrylate polymer 0 - 20.0%
alkali metal silicate 0 - 40.0%
liquid nonionic surfactant 0 - 15.0%
phosphate-free builder salt 10.0 - 65.0%
anti-foaming agent 0 - 1.5%
protease enzyme 0.5 - 15.0%
amylase enzyme 0.3 - 8.0%
low molecular weight polyacrylate polymer 0 - 20.0%
alkali metal silicate 0 - 40.0%
liquid nonionic surfactant 0 - 15.0%
phosphate-free builder salt 10.0 - 65.0%
anti-foaming agent 0 - 1.5%
protease enzyme 0.5 - 15.0%
amylase enzyme 0.3 - 8.0%
11. The concentrated powdered dishwashing composition according to claim 1 which includes about 0.1 to 1.2 weight percent of an anti-foaming agent.
12. The concentrated powdered dishwashing composition according to claim 1, wherein said protease enzyme is Maxapem 30 and Maxapem 42 proteases enzyme and said amylase enzyme is Maxamyl amylase enzyme, a weight ratio of said protease enzyme to said amylase enzyme being 5:1 to 1.1:1, wherein said detergent dishwashing composition has a pH of less than 10.5.
13. The concentrated powdered dishwashing composition according to claim 1, wherein said proteast enzyme is Maxatase protease enzyme and said amylase enzyme is Maxamyl amylase enzyme, a weight ratio of sait protease enzyme to said amylase enzyme being 5:1 to 1.1:1, wherein said detergent dishwashing composition has a pH of less than 10.5.
Applications Claiming Priority (4)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US70856591A | 1991-05-31 | 1991-05-31 | |
US70856991A | 1991-05-31 | 1991-05-31 | |
US7/708,565 | 1991-05-31 | ||
US7/708,569 | 1991-05-31 |
Publications (1)
Publication Number | Publication Date |
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CA2069853A1 true CA2069853A1 (en) | 1992-12-01 |
Family
ID=27108118
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
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CA002069853A Abandoned CA2069853A1 (en) | 1991-05-31 | 1992-05-28 | Phosphate-containing powder automatic dishwashing composition with enzymes |
Country Status (9)
Country | Link |
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EP (1) | EP0516554A3 (en) |
AU (1) | AU654184B2 (en) |
CA (1) | CA2069853A1 (en) |
FI (1) | FI922491A (en) |
FR (1) | FR2689901B1 (en) |
GR (1) | GR920100231A (en) |
NO (1) | NO922050L (en) |
NZ (1) | NZ242839A (en) |
PT (1) | PT100535A (en) |
Families Citing this family (14)
Publication number | Priority date | Publication date | Assignee | Title |
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US5173207A (en) * | 1991-05-31 | 1992-12-22 | Colgate-Palmolive Company | Powered automatic dishwashing composition containing enzymes |
AU656375B2 (en) * | 1991-05-31 | 1995-02-02 | Colgate-Palmolive Company, The | Powdered automatic dishwashing composition containing enzymes |
GB2295622A (en) * | 1994-11-29 | 1996-06-05 | Procter & Gamble | Silicate based machine dishwashing detergent composition |
US5703027A (en) * | 1994-11-29 | 1997-12-30 | The Procter & Gamble Company | Monomeric rich silicate system in automatic dishwashing composition with improved glass etching |
GB2295625A (en) * | 1994-11-29 | 1996-06-05 | Procter & Gamble | Bleaching composition for machine dishwashing |
AU5288299A (en) * | 1998-08-07 | 2000-02-28 | Holson, Sylvester | Highly alkaline warewashing detergent and method of manufacture thereof |
WO2001000766A1 (en) * | 1999-06-25 | 2001-01-04 | Unilever Plc | Dish washing process and compositions relating thereto |
CN101679987A (en) | 2007-03-09 | 2010-03-24 | 丹尼斯科美国公司 | Alkaliphilic bacillus species alpha-amylase variants, compositions comprising alpha-amylase variants, and methods of use |
ES2316286B1 (en) * | 2007-06-26 | 2010-02-05 | Universidad De Granada | DETERGENTS FOR HARD SURFACES. |
DK2297312T3 (en) | 2008-06-06 | 2013-12-16 | Danisco Us Inc | Alpha-amylase variants of Bacillus subtilis and methods for their use |
EP2291526B1 (en) | 2008-06-06 | 2014-08-13 | Danisco US Inc. | Saccharification enzyme composition with Bacillus subtilis alpha-amylase |
US9040278B2 (en) | 2008-06-06 | 2015-05-26 | Danisco Us Inc. | Production of glucose from starch using alpha-amylases from Bacillus subtilis |
WO2010036515A1 (en) | 2008-09-25 | 2010-04-01 | Danisco Us Inc. | Alpha-amylase blends and methods for using said blends |
EP2491121A2 (en) | 2009-10-23 | 2012-08-29 | Danisco US Inc. | Methods for reducing blue saccharide |
Family Cites Families (4)
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GB8321923D0 (en) * | 1983-08-15 | 1983-09-14 | Unilever Plc | Machine-dishwashing compositions |
GB8328075D0 (en) * | 1983-10-20 | 1983-11-23 | Unilever Plc | Dishwashing compositions |
US4810413A (en) * | 1987-05-29 | 1989-03-07 | The Procter & Gamble Company | Particles containing ammonium salts or other chlorine scavengers for detergent compositions |
GB8923788D0 (en) * | 1989-10-23 | 1989-12-13 | Unilever Plc | Enzymatic detergent compositions and their use |
-
1992
- 1992-05-11 AU AU16166/92A patent/AU654184B2/en not_active Ceased
- 1992-05-20 NZ NZ242839A patent/NZ242839A/en unknown
- 1992-05-25 NO NO92922050A patent/NO922050L/en unknown
- 1992-05-28 CA CA002069853A patent/CA2069853A1/en not_active Abandoned
- 1992-05-29 FI FI922491A patent/FI922491A/en not_active Application Discontinuation
- 1992-05-29 GR GR920100231A patent/GR920100231A/en unknown
- 1992-05-29 EP EP19920401475 patent/EP0516554A3/en not_active Withdrawn
- 1992-05-29 PT PT100535A patent/PT100535A/en not_active Application Discontinuation
- 1992-06-01 FR FR9206615A patent/FR2689901B1/en not_active Expired - Lifetime
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EP0516554A2 (en) | 1992-12-02 |
EP0516554A3 (en) | 1994-07-13 |
FI922491A0 (en) | 1992-05-29 |
AU654184B2 (en) | 1994-10-27 |
NO922050L (en) | 1992-12-01 |
AU1616692A (en) | 1992-12-03 |
NO922050D0 (en) | 1992-05-25 |
PT100535A (en) | 1994-01-31 |
FI922491A (en) | 1992-12-01 |
FR2689901A1 (en) | 1993-10-15 |
NZ242839A (en) | 1995-04-27 |
GR920100231A (en) | 1993-03-31 |
FR2689901B1 (en) | 1995-05-05 |
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