US3600319A - Process for application of enzymes to spray-dried detergent granules - Google Patents
Process for application of enzymes to spray-dried detergent granules Download PDFInfo
- Publication number
- US3600319A US3600319A US739827A US3600319DA US3600319A US 3600319 A US3600319 A US 3600319A US 739827 A US739827 A US 739827A US 3600319D A US3600319D A US 3600319DA US 3600319 A US3600319 A US 3600319A
- Authority
- US
- United States
- Prior art keywords
- enzyme
- granules
- spray
- enzymes
- detergent
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Expired - Lifetime
Links
- 102000004190 Enzymes Human genes 0.000 title abstract description 117
- 108090000790 Enzymes Proteins 0.000 title abstract description 117
- 239000008187 granular material Substances 0.000 title abstract description 70
- 239000003599 detergent Substances 0.000 title abstract description 44
- 238000000034 method Methods 0.000 title description 29
- 230000008569 process Effects 0.000 title description 22
- 239000002002 slurry Substances 0.000 abstract description 31
- 239000007788 liquid Substances 0.000 abstract description 25
- 238000005507 spraying Methods 0.000 abstract description 5
- 229940088598 enzyme Drugs 0.000 description 115
- 239000003981 vehicle Substances 0.000 description 34
- 239000000047 product Substances 0.000 description 22
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 21
- 239000002689 soil Substances 0.000 description 20
- 239000000843 powder Substances 0.000 description 18
- 239000004365 Protease Substances 0.000 description 16
- 102000035195 Peptidases Human genes 0.000 description 15
- 108091005804 Peptidases Proteins 0.000 description 15
- 239000000203 mixture Substances 0.000 description 14
- 239000007921 spray Substances 0.000 description 14
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 14
- CSCPPACGZOOCGX-UHFFFAOYSA-N Acetone Chemical compound CC(C)=O CSCPPACGZOOCGX-UHFFFAOYSA-N 0.000 description 12
- OKKJLVBELUTLKV-UHFFFAOYSA-N Methanol Chemical compound OC OKKJLVBELUTLKV-UHFFFAOYSA-N 0.000 description 12
- 108010056079 Subtilisins Proteins 0.000 description 12
- 102000005158 Subtilisins Human genes 0.000 description 12
- 239000002304 perfume Substances 0.000 description 11
- 239000000344 soap Substances 0.000 description 11
- -1 alkali metal salts Chemical class 0.000 description 10
- UHOVQNZJYSORNB-UHFFFAOYSA-N Benzene Chemical compound C1=CC=CC=C1 UHOVQNZJYSORNB-UHFFFAOYSA-N 0.000 description 9
- BPQQTUXANYXVAA-UHFFFAOYSA-N Orthosilicate Chemical compound [O-][Si]([O-])([O-])[O-] BPQQTUXANYXVAA-UHFFFAOYSA-N 0.000 description 9
- VLKZOEOYAKHREP-UHFFFAOYSA-N n-Hexane Chemical compound CCCCCC VLKZOEOYAKHREP-UHFFFAOYSA-N 0.000 description 9
- KFZMGEQAYNKOFK-UHFFFAOYSA-N Isopropanol Chemical compound CC(C)O KFZMGEQAYNKOFK-UHFFFAOYSA-N 0.000 description 8
- 230000015556 catabolic process Effects 0.000 description 8
- 239000002245 particle Substances 0.000 description 8
- 239000000271 synthetic detergent Substances 0.000 description 8
- 235000019419 proteases Nutrition 0.000 description 7
- 150000003839 salts Chemical class 0.000 description 7
- 102000004157 Hydrolases Human genes 0.000 description 6
- 108090000604 Hydrolases Proteins 0.000 description 6
- 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 6
- 239000004115 Sodium Silicate Substances 0.000 description 6
- FAPWRFPIFSIZLT-UHFFFAOYSA-M Sodium chloride Chemical compound [Na+].[Cl-] FAPWRFPIFSIZLT-UHFFFAOYSA-M 0.000 description 6
- HEMHJVSKTPXQMS-UHFFFAOYSA-M Sodium hydroxide Chemical compound [OH-].[Na+] HEMHJVSKTPXQMS-UHFFFAOYSA-M 0.000 description 6
- YXFVVABEGXRONW-UHFFFAOYSA-N Toluene Chemical compound CC1=CC=CC=C1 YXFVVABEGXRONW-UHFFFAOYSA-N 0.000 description 6
- OSGAYBCDTDRGGQ-UHFFFAOYSA-L calcium sulfate Chemical compound [Ca+2].[O-]S([O-])(=O)=O OSGAYBCDTDRGGQ-UHFFFAOYSA-L 0.000 description 6
- 150000001875 compounds Chemical class 0.000 description 6
- 239000012530 fluid Substances 0.000 description 6
- 239000011734 sodium Substances 0.000 description 6
- NTHWMYGWWRZVTN-UHFFFAOYSA-N sodium silicate Chemical compound [Na+].[Na+].[O-][Si]([O-])=O NTHWMYGWWRZVTN-UHFFFAOYSA-N 0.000 description 6
- 229910052911 sodium silicate Inorganic materials 0.000 description 6
- 235000019832 sodium triphosphate Nutrition 0.000 description 6
- 238000001704 evaporation Methods 0.000 description 5
- 230000008020 evaporation Effects 0.000 description 5
- 230000036571 hydration Effects 0.000 description 5
- 238000006703 hydration reaction Methods 0.000 description 5
- 239000000463 material Substances 0.000 description 5
- 239000000758 substrate Substances 0.000 description 5
- 108090000371 Esterases Proteins 0.000 description 4
- IMNFDUFMRHMDMM-UHFFFAOYSA-N N-Heptane Chemical compound CCCCCCC IMNFDUFMRHMDMM-UHFFFAOYSA-N 0.000 description 4
- 239000002253 acid Substances 0.000 description 4
- 125000000129 anionic group Chemical group 0.000 description 4
- 238000009835 boiling Methods 0.000 description 4
- 238000004140 cleaning Methods 0.000 description 4
- 238000006731 degradation reaction Methods 0.000 description 4
- 230000000593 degrading effect Effects 0.000 description 4
- ZXEKIIBDNHEJCQ-UHFFFAOYSA-N isobutanol Chemical compound CC(C)CO ZXEKIIBDNHEJCQ-UHFFFAOYSA-N 0.000 description 4
- 238000004900 laundering Methods 0.000 description 4
- 238000004519 manufacturing process Methods 0.000 description 4
- 229910052708 sodium Inorganic materials 0.000 description 4
- 229910052938 sodium sulfate Inorganic materials 0.000 description 4
- 235000011152 sodium sulphate Nutrition 0.000 description 4
- 238000003860 storage Methods 0.000 description 4
- 239000000126 substance Substances 0.000 description 4
- 108010065511 Amylases Proteins 0.000 description 3
- 102000013142 Amylases Human genes 0.000 description 3
- ZMXDDKWLCZADIW-UHFFFAOYSA-N N,N-Dimethylformamide Chemical compound CN(C)C=O ZMXDDKWLCZADIW-UHFFFAOYSA-N 0.000 description 3
- 101710163270 Nuclease Proteins 0.000 description 3
- 102000012479 Serine Proteases Human genes 0.000 description 3
- 108010022999 Serine Proteases Proteins 0.000 description 3
- 108090000787 Subtilisin Proteins 0.000 description 3
- 108010089934 carbohydrase Proteins 0.000 description 3
- 239000003795 chemical substances by application Substances 0.000 description 3
- 235000014113 dietary fatty acids Nutrition 0.000 description 3
- 230000000694 effects Effects 0.000 description 3
- 230000002255 enzymatic effect Effects 0.000 description 3
- 239000000194 fatty acid Substances 0.000 description 3
- 229930195729 fatty acid Natural products 0.000 description 3
- 150000004665 fatty acids Chemical class 0.000 description 3
- 239000004615 ingredient Substances 0.000 description 3
- 239000000320 mechanical mixture Substances 0.000 description 3
- 230000007935 neutral effect Effects 0.000 description 3
- BDERNNFJNOPAEC-UHFFFAOYSA-N propan-1-ol Chemical compound CCCO BDERNNFJNOPAEC-UHFFFAOYSA-N 0.000 description 3
- 102000004169 proteins and genes Human genes 0.000 description 3
- 108090000623 proteins and genes Proteins 0.000 description 3
- 239000011780 sodium chloride Substances 0.000 description 3
- DZCAZXAJPZCSCU-UHFFFAOYSA-K sodium nitrilotriacetate Chemical compound [Na+].[Na+].[Na+].[O-]C(=O)CN(CC([O-])=O)CC([O-])=O DZCAZXAJPZCSCU-UHFFFAOYSA-K 0.000 description 3
- 239000002904 solvent Substances 0.000 description 3
- 238000001694 spray drying Methods 0.000 description 3
- WSLDOOZREJYCGB-UHFFFAOYSA-N 1,2-Dichloroethane Chemical compound ClCCCl WSLDOOZREJYCGB-UHFFFAOYSA-N 0.000 description 2
- ZWEHNKRNPOVVGH-UHFFFAOYSA-N 2-Butanone Chemical class CCC(C)=O ZWEHNKRNPOVVGH-UHFFFAOYSA-N 0.000 description 2
- 108090000145 Bacillolysin Proteins 0.000 description 2
- 241000894006 Bacteria Species 0.000 description 2
- 108010004032 Bromelains Proteins 0.000 description 2
- 244000060011 Cocos nucifera Species 0.000 description 2
- 235000013162 Cocos nucifera Nutrition 0.000 description 2
- RTZKZFJDLAIYFH-UHFFFAOYSA-N Diethyl ether Chemical compound CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 description 2
- IAZDPXIOMUYVGZ-UHFFFAOYSA-N Dimethylsulphoxide Chemical compound CS(C)=O IAZDPXIOMUYVGZ-UHFFFAOYSA-N 0.000 description 2
- 241000233866 Fungi Species 0.000 description 2
- 108090001060 Lipase Proteins 0.000 description 2
- 102000004882 Lipase Human genes 0.000 description 2
- 239000004367 Lipase Substances 0.000 description 2
- LRHPLDYGYMQRHN-UHFFFAOYSA-N N-Butanol Chemical compound CCCCO LRHPLDYGYMQRHN-UHFFFAOYSA-N 0.000 description 2
- 108091005507 Neutral proteases Proteins 0.000 description 2
- 102000035092 Neutral proteases Human genes 0.000 description 2
- 108010059712 Pronase Proteins 0.000 description 2
- PMZURENOXWZQFD-UHFFFAOYSA-L Sodium Sulfate Chemical compound [Na+].[Na+].[O-]S([O-])(=O)=O PMZURENOXWZQFD-UHFFFAOYSA-L 0.000 description 2
- DPXJVFZANSGRMM-UHFFFAOYSA-N acetic acid;2,3,4,5,6-pentahydroxyhexanal;sodium Chemical compound [Na].CC(O)=O.OCC(O)C(O)C(O)C(O)C=O DPXJVFZANSGRMM-UHFFFAOYSA-N 0.000 description 2
- 150000001298 alcohols Chemical class 0.000 description 2
- 150000001335 aliphatic alkanes Chemical class 0.000 description 2
- 229910052783 alkali metal Inorganic materials 0.000 description 2
- 235000019418 amylase Nutrition 0.000 description 2
- 150000004945 aromatic hydrocarbons Chemical class 0.000 description 2
- 239000001768 carboxy methyl cellulose Substances 0.000 description 2
- 239000004744 fabric Substances 0.000 description 2
- 238000009472 formulation Methods 0.000 description 2
- 229930195733 hydrocarbon Natural products 0.000 description 2
- 230000007062 hydrolysis Effects 0.000 description 2
- 238000006460 hydrolysis reaction Methods 0.000 description 2
- 150000002576 ketones Chemical class 0.000 description 2
- 235000019421 lipase Nutrition 0.000 description 2
- 229920005646 polycarboxylate Polymers 0.000 description 2
- 108090000765 processed proteins & peptides Proteins 0.000 description 2
- 230000002035 prolonged effect Effects 0.000 description 2
- 238000005204 segregation Methods 0.000 description 2
- CDBYLPFSWZWCQE-UHFFFAOYSA-L sodium carbonate Substances [Na+].[Na+].[O-]C([O-])=O CDBYLPFSWZWCQE-UHFFFAOYSA-L 0.000 description 2
- 235000019812 sodium carboxymethyl cellulose Nutrition 0.000 description 2
- 229920001027 sodium carboxymethylcellulose Polymers 0.000 description 2
- 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 2
- 235000011121 sodium hydroxide Nutrition 0.000 description 2
- UCSJYZPVAKXKNQ-HZYVHMACSA-N streptomycin Chemical compound CN[C@H]1[C@H](O)[C@@H](O)[C@H](CO)O[C@H]1O[C@@H]1[C@](C=O)(O)[C@H](C)O[C@H]1O[C@@H]1[C@@H](NC(N)=N)[C@H](O)[C@@H](NC(N)=N)[C@H](O)[C@H]1O UCSJYZPVAKXKNQ-HZYVHMACSA-N 0.000 description 2
- 235000019818 tetrasodium diphosphate Nutrition 0.000 description 2
- UCTWMZQNUQWSLP-VIFPVBQESA-N (R)-adrenaline Chemical compound CNC[C@H](O)C1=CC=C(O)C(O)=C1 UCTWMZQNUQWSLP-VIFPVBQESA-N 0.000 description 1
- CLHYKAZPWIRRRD-UHFFFAOYSA-N 1-hydroxypropane-1-sulfonic acid Chemical compound CCC(O)S(O)(=O)=O CLHYKAZPWIRRRD-UHFFFAOYSA-N 0.000 description 1
- 102000004400 Aminopeptidases Human genes 0.000 description 1
- 108090000915 Aminopeptidases Proteins 0.000 description 1
- 239000004382 Amylase Substances 0.000 description 1
- 241000193830 Bacillus <bacterium> Species 0.000 description 1
- 244000063299 Bacillus subtilis Species 0.000 description 1
- 235000014469 Bacillus subtilis Nutrition 0.000 description 1
- 108091005658 Basic proteases Proteins 0.000 description 1
- LSNNMFCWUKXFEE-UHFFFAOYSA-M Bisulfite Chemical compound OS([O-])=O LSNNMFCWUKXFEE-UHFFFAOYSA-M 0.000 description 1
- OYPRJOBELJOOCE-UHFFFAOYSA-N Calcium Chemical compound [Ca] OYPRJOBELJOOCE-UHFFFAOYSA-N 0.000 description 1
- 102000003670 Carboxypeptidase B Human genes 0.000 description 1
- 108090000087 Carboxypeptidase B Proteins 0.000 description 1
- 102000000496 Carboxypeptidases A Human genes 0.000 description 1
- 108010080937 Carboxypeptidases A Proteins 0.000 description 1
- 108010059892 Cellulase Proteins 0.000 description 1
- 108090000322 Cholinesterases Proteins 0.000 description 1
- 102000003914 Cholinesterases Human genes 0.000 description 1
- 108090000317 Chymotrypsin Proteins 0.000 description 1
- 108060005980 Collagenase Proteins 0.000 description 1
- 102000029816 Collagenase Human genes 0.000 description 1
- 229920002261 Corn starch Polymers 0.000 description 1
- 108010053770 Deoxyribonucleases Proteins 0.000 description 1
- 102000016911 Deoxyribonucleases Human genes 0.000 description 1
- 241000196324 Embryophyta Species 0.000 description 1
- IAYPIBMASNFSPL-UHFFFAOYSA-N Ethylene oxide Chemical compound C1CO1 IAYPIBMASNFSPL-UHFFFAOYSA-N 0.000 description 1
- 102100031416 Gastric triacylglycerol lipase Human genes 0.000 description 1
- 241000243328 Hydridae Species 0.000 description 1
- 102000004867 Hydro-Lyases Human genes 0.000 description 1
- 108090001042 Hydro-Lyases Proteins 0.000 description 1
- 102000004195 Isomerases Human genes 0.000 description 1
- 108090000769 Isomerases Proteins 0.000 description 1
- 101710098554 Lipase B Proteins 0.000 description 1
- 102000004317 Lyases Human genes 0.000 description 1
- 108090000856 Lyases Proteins 0.000 description 1
- 108010014251 Muramidase Proteins 0.000 description 1
- 102000016943 Muramidase Human genes 0.000 description 1
- 108010062010 N-Acetylmuramoyl-L-alanine Amidase Proteins 0.000 description 1
- 102000004316 Oxidoreductases Human genes 0.000 description 1
- 108090000854 Oxidoreductases Proteins 0.000 description 1
- 108010067372 Pancreatic elastase Proteins 0.000 description 1
- 102000016387 Pancreatic elastase Human genes 0.000 description 1
- 108050006759 Pancreatic lipases Proteins 0.000 description 1
- 102000019280 Pancreatic lipases Human genes 0.000 description 1
- 108010019160 Pancreatin Proteins 0.000 description 1
- 108010067035 Pancrelipase Proteins 0.000 description 1
- 108090000526 Papain Proteins 0.000 description 1
- 108090000284 Pepsin A Proteins 0.000 description 1
- 102000057297 Pepsin A Human genes 0.000 description 1
- ISWSIDIOOBJBQZ-UHFFFAOYSA-N Phenol Chemical compound OC1=CC=CC=C1 ISWSIDIOOBJBQZ-UHFFFAOYSA-N 0.000 description 1
- 108010064785 Phospholipases Proteins 0.000 description 1
- 102000015439 Phospholipases Human genes 0.000 description 1
- 108010059820 Polygalacturonase Proteins 0.000 description 1
- 229920000388 Polyphosphate Polymers 0.000 description 1
- 108010083644 Ribonucleases Proteins 0.000 description 1
- 102000006382 Ribonucleases Human genes 0.000 description 1
- 229920002472 Starch Polymers 0.000 description 1
- 241000187392 Streptomyces griseus Species 0.000 description 1
- QAOWNCQODCNURD-UHFFFAOYSA-L Sulfate Chemical compound [O-]S([O-])(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-L 0.000 description 1
- 102000004357 Transferases Human genes 0.000 description 1
- 108090000992 Transferases Proteins 0.000 description 1
- 108090000631 Trypsin Proteins 0.000 description 1
- 102000004142 Trypsin Human genes 0.000 description 1
- HCHKCACWOHOZIP-UHFFFAOYSA-N Zinc Chemical compound [Zn] HCHKCACWOHOZIP-UHFFFAOYSA-N 0.000 description 1
- PXMYLRYKRSAYNM-UHFFFAOYSA-M [Na+].CC.OOP(=O)OP([O-])=O Chemical compound [Na+].CC.OOP(=O)OP([O-])=O PXMYLRYKRSAYNM-UHFFFAOYSA-M 0.000 description 1
- 239000011149 active material Substances 0.000 description 1
- 239000000654 additive Substances 0.000 description 1
- 238000005054 agglomeration Methods 0.000 description 1
- 230000002776 aggregation Effects 0.000 description 1
- 150000001340 alkali metals Chemical class 0.000 description 1
- 150000008051 alkyl sulfates Chemical class 0.000 description 1
- 108010028144 alpha-Glucosidases Proteins 0.000 description 1
- 102000016679 alpha-Glucosidases Human genes 0.000 description 1
- 230000004075 alteration Effects 0.000 description 1
- 229940025131 amylases Drugs 0.000 description 1
- 108090000987 aspergillopepsin I Proteins 0.000 description 1
- 239000012298 atmosphere Substances 0.000 description 1
- 125000004429 atom Chemical group 0.000 description 1
- 230000008901 benefit Effects 0.000 description 1
- 108010051210 beta-Fructofuranosidase Proteins 0.000 description 1
- 235000019835 bromelain Nutrition 0.000 description 1
- 229910052791 calcium Inorganic materials 0.000 description 1
- 239000011575 calcium Substances 0.000 description 1
- 159000000007 calcium salts Chemical class 0.000 description 1
- 150000001720 carbohydrates Chemical class 0.000 description 1
- 235000014633 carbohydrates Nutrition 0.000 description 1
- 125000004432 carbon atom Chemical group C* 0.000 description 1
- 125000003178 carboxy group Chemical group [H]OC(*)=O 0.000 description 1
- 229940106157 cellulase Drugs 0.000 description 1
- 239000007795 chemical reaction product Substances 0.000 description 1
- 229960002376 chymotrypsin Drugs 0.000 description 1
- 239000004927 clay Substances 0.000 description 1
- 229910052570 clay Inorganic materials 0.000 description 1
- 235000019864 coconut oil Nutrition 0.000 description 1
- 239000003240 coconut oil Substances 0.000 description 1
- 229960002424 collagenase Drugs 0.000 description 1
- 239000013065 commercial product Substances 0.000 description 1
- 239000012141 concentrate Substances 0.000 description 1
- 239000007859 condensation product Substances 0.000 description 1
- 239000008120 corn starch Substances 0.000 description 1
- HPXRVTGHNJAIIH-UHFFFAOYSA-N cyclohexanol Chemical compound OC1CCCCC1 HPXRVTGHNJAIIH-UHFFFAOYSA-N 0.000 description 1
- 229940109357 desoxyribonuclease Drugs 0.000 description 1
- 229940111205 diastase Drugs 0.000 description 1
- 239000003085 diluting agent Substances 0.000 description 1
- 125000000118 dimethyl group Chemical group [H]C([H])([H])* 0.000 description 1
- KWKXNDCHNDYVRT-UHFFFAOYSA-N dodecylbenzene Chemical compound CCCCCCCCCCCCC1=CC=CC=C1 KWKXNDCHNDYVRT-UHFFFAOYSA-N 0.000 description 1
- 239000000975 dye Substances 0.000 description 1
- 238000005538 encapsulation Methods 0.000 description 1
- 238000005516 engineering process Methods 0.000 description 1
- 230000007613 environmental effect Effects 0.000 description 1
- 150000002148 esters Chemical class 0.000 description 1
- 108010093305 exopolygalacturonase Proteins 0.000 description 1
- 150000002191 fatty alcohols Chemical class 0.000 description 1
- 238000000855 fermentation Methods 0.000 description 1
- 230000004151 fermentation Effects 0.000 description 1
- 238000001914 filtration Methods 0.000 description 1
- 238000000915 furnace ionisation nonthermal excitation spectrometry Methods 0.000 description 1
- 108010091264 gastric triacylglycerol lipase Proteins 0.000 description 1
- 230000002070 germicidal effect Effects 0.000 description 1
- 239000011256 inorganic filler Substances 0.000 description 1
- 229910003475 inorganic filler Inorganic materials 0.000 description 1
- 235000011073 invertase Nutrition 0.000 description 1
- 108010059345 keratinase Proteins 0.000 description 1
- 150000002632 lipids Chemical class 0.000 description 1
- 229960000274 lysozyme Drugs 0.000 description 1
- 239000004325 lysozyme Substances 0.000 description 1
- 235000010335 lysozyme Nutrition 0.000 description 1
- 230000014759 maintenance of location Effects 0.000 description 1
- 244000005700 microbiome Species 0.000 description 1
- 238000012986 modification Methods 0.000 description 1
- 230000004048 modification Effects 0.000 description 1
- 230000035772 mutation Effects 0.000 description 1
- 102000039446 nucleic acids Human genes 0.000 description 1
- 108020004707 nucleic acids Proteins 0.000 description 1
- 150000007523 nucleic acids Chemical class 0.000 description 1
- TVMXDCGIABBOFY-UHFFFAOYSA-N octane Chemical compound CCCCCCCC TVMXDCGIABBOFY-UHFFFAOYSA-N 0.000 description 1
- 230000003287 optical effect Effects 0.000 description 1
- 108090000021 oryzin Proteins 0.000 description 1
- 229940116369 pancreatic lipase Drugs 0.000 description 1
- 229940055695 pancreatin Drugs 0.000 description 1
- 229940055729 papain Drugs 0.000 description 1
- 235000019834 papain Nutrition 0.000 description 1
- 229940111202 pepsin Drugs 0.000 description 1
- 125000000864 peroxy group Chemical group O(O*)* 0.000 description 1
- 229920001184 polypeptide Polymers 0.000 description 1
- 239000001205 polyphosphate Substances 0.000 description 1
- 235000011176 polyphosphates Nutrition 0.000 description 1
- 238000002360 preparation method Methods 0.000 description 1
- 125000002924 primary amino group Chemical group [H]N([H])* 0.000 description 1
- 102000004196 processed proteins & peptides Human genes 0.000 description 1
- 230000002797 proteolythic effect Effects 0.000 description 1
- 238000005086 pumping Methods 0.000 description 1
- 239000011347 resin Substances 0.000 description 1
- 229920005989 resin Polymers 0.000 description 1
- 229910000029 sodium carbonate Inorganic materials 0.000 description 1
- 229940048086 sodium pyrophosphate Drugs 0.000 description 1
- 239000003381 stabilizer Substances 0.000 description 1
- 239000008107 starch Substances 0.000 description 1
- 235000019698 starch Nutrition 0.000 description 1
- 229960005322 streptomycin Drugs 0.000 description 1
- BDHFUVZGWQCTTF-UHFFFAOYSA-M sulfonate Chemical compound [O-]S(=O)=O BDHFUVZGWQCTTF-UHFFFAOYSA-M 0.000 description 1
- QAOWNCQODCNURD-UHFFFAOYSA-N sulfuric acid Substances OS(O)(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-N 0.000 description 1
- 239000000375 suspending agent Substances 0.000 description 1
- 239000003760 tallow Substances 0.000 description 1
- 239000001577 tetrasodium phosphonato phosphate Substances 0.000 description 1
- UEUXEKPTXMALOB-UHFFFAOYSA-J tetrasodium;2-[2-[bis(carboxylatomethyl)amino]ethyl-(carboxylatomethyl)amino]acetate Chemical compound [Na+].[Na+].[Na+].[Na+].[O-]C(=O)CN(CC([O-])=O)CCN(CC([O-])=O)CC([O-])=O UEUXEKPTXMALOB-UHFFFAOYSA-J 0.000 description 1
- RYFMWSXOAZQYPI-UHFFFAOYSA-K trisodium phosphate Chemical compound [Na+].[Na+].[Na+].[O-]P([O-])([O-])=O RYFMWSXOAZQYPI-UHFFFAOYSA-K 0.000 description 1
- KCYJBQNPOFBNHE-UHFFFAOYSA-K trisodium;hydroxy-(1-hydroxy-1-phosphonatoethyl)phosphinate Chemical compound [Na+].[Na+].[Na+].OP(=O)([O-])C(O)(C)P([O-])([O-])=O KCYJBQNPOFBNHE-UHFFFAOYSA-K 0.000 description 1
- 239000012588 trypsin Substances 0.000 description 1
- 229960001322 trypsin Drugs 0.000 description 1
- 238000013022 venting Methods 0.000 description 1
- 238000005406 washing Methods 0.000 description 1
- 229910052725 zinc Inorganic materials 0.000 description 1
- 239000011701 zinc Substances 0.000 description 1
Images
Classifications
-
- C—CHEMISTRY; METALLURGY
- C11—ANIMAL OR VEGETABLE OILS, FATS, FATTY SUBSTANCES OR WAXES; FATTY ACIDS THEREFROM; DETERGENTS; CANDLES
- C11D—DETERGENT COMPOSITIONS; USE OF SINGLE SUBSTANCES AS DETERGENTS; SOAP OR SOAP-MAKING; RESIN SOAPS; RECOVERY OF GLYCEROL
- C11D3/00—Other compounding ingredients of detergent compositions covered in group C11D1/00
- C11D3/16—Organic compounds
- C11D3/38—Products with no well-defined composition, e.g. natural products
- C11D3/386—Preparations containing enzymes, e.g. protease or amylase
- C11D3/38672—Granulated or coated enzymes
-
- 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
- C11D11/00—Special methods for preparing compositions containing mixtures of detergents
- C11D11/0082—Special methods for preparing compositions containing mixtures of detergents one or more of the detergent ingredients being in a liquefied state, e.g. slurry, paste or melt, and the process resulting in solid detergent particles such as granules, powders or beads
- C11D11/0088—Special methods for preparing compositions containing mixtures of detergents one or more of the detergent ingredients being in a liquefied state, e.g. slurry, paste or melt, and the process resulting in solid detergent particles such as granules, powders or beads the liquefied ingredients being sprayed or adsorbed onto solid particles
Definitions
- This invention relates to a method for applying enzymes to laundry detergent granules from an organic liquid vehicle.
- Enzymes aid in laundering by attacking soil and stains found on soiled fabrics. Soils and stains are decomposed or altered in such an attack so as to render them more removable during laundering. Enzymes are usually used as a component of a laundry detergent formulation containing conventional cleaning ingredients, such as builders and organic detergents. The enzymes suitable for such laundry uses are usually found in a fine powder form. Enzymes are expensive and powerful materials which must be judiciously formulated and used. Such fine powders of concentrated materials are difficult to handle, measure and formulate.
- enzyme-containing laundry products are mechanical mixtures of a fine enzyme powder and other granular materials. Enzyme powder in such mechanical mixtures tends to segregate, resulting in a non-uniform product. Non-uniformity results in an undependable product in use.
- Such mechanical mixtures also present stability problems resulting from the mobility of the enzyme powder in the mixture; it is exposed to some cleaning ingredients and environmental condition which may either attack the enzyme or aid it in degrading itself. For example, moisture tends to cause the enzyme to degrade itself; many enzymes are incompatible with highly alkaline detergent materials such as caustic soda and sodium silicate, particularly in the presence of moisture.
- Warm and moisttemperatures within the spray tower usually range from about 600 F. at the air inlet to about 160 F. at the air exit;
- the enzyme is applied and firmly attached to the granules in a way which is efficient, which can utilize existing equipment, which does not unduly expose the enzyme to the degrading effects of heat and moisture-supported alkalinity and which provides a stable non-segregating product.
- the application technique of the process of this invention is shown in the schematic drawing which is described in Example I.
- the spray-dried granular detergent composition to which enzymes are applied by the process of this invention consists essentially of an organic detergent, an alkaline builder and sodium silicate.
- the organic detergent and alkaline builder range in weight ratio from about 2:1 to about 1:10, preferably 1:2 to 1:6. Together they comprise about 40% to about 97%, preferably 50% to of the spray-dried granules.
- These granules contain from about 3% to about 20%, preferably 5% to 10%, sodium silicate having a SiO zNa O ratio ranging from about 3.621 to about 1:1, preferably from 2.011 to 16:1.
- the granules have a pH in water solution of about 9 to 12, generally 9.5 to 11.5.
- the granules range in particle size from about .075 mm. to about 3.33 mm. (through 6 mesh and on 200 mesh-Tyler standard screens), preferably from 0.2 mm. to 2 mm. They range in density from about 0.2 gram/cc. to about 0.8 gram/cc.
- the granules should have a free moisture content of less than 5% and preferably less than 2% in order to reduce attack on the enzyme by the silicate. Free moisture is moisture other than water of hydration in the granular components.
- the organic detergent compounds used in the spraydried granular detergent used in this invention are of the usual water-soluble anionic non-soap, nonionic, ampholytic and zwitterionic synthetic detergent classes or fatty acid soap.
- anionic non-soap synthetic class in the form of their alkali metal salts, are preferred.
- This class is usually characterized as organic sulfuric reaction products having in their molecular structure an alkyl radical containing from 8-22 carbon atoms and a sulfonic acid or sulfuric acid ester radical. This class is preferred because it is more readily spray dried than the other and has the best detergency characteristics. All of the above subclasses are described in additional detail in US. Pat. 3,351,558 issued to Roger E. Zimmerer Nov. 7, 1967, particularly from line 59, column 6 to line 74, column 9. This description is incorporated herein by reference.
- alkaline builders of the spray-dried detergent granules are of the usual classes, both inorganic and organic.
- the preferred classes of alkaline builder salts are the water-soluble alkali metal polyphosphates, aminopolyacetates, polyphosphonates and polycarboxylates.
- Representative examples of builder compounds of these classes are as follows: sodium tripolyphosphate, sodium pyrophosphate, sodium ethylenediaminetetraacetate, sodium nitrilotriacetate, sodium ethane hydroxy diphosphonate, sodium ethane-l-hydroxy-l,1,2-triphosphonate, and the polycarboxylates described in the patent of Francis L. Diehl, US. 3,308,067, issued Mar. 7, 1967.
- Other examples of suitable builders can be found in Zimmerers US. Pat. 3,351,- 558, especially from line 64, column 2 to line 38, column 3 which is incorporated herein by reference.
- the spray-dried detergent granules can contain any of the other usual optional additives for such products including any of the following: inorganic fillers such as sodium sulfate in an amount up to about 35%; effective amounts of soil suspending agents such as sodium carboxymethyl cellulose, optical brighteners, dyes, germicidal agents, suds depressants, suds boosters, peroxy compounds, perfume and alkalinity agents such as NaOH, sodium carbonate or trisodium orthophosphate.
- inorganic fillers such as sodium sulfate in an amount up to about 35%
- effective amounts of soil suspending agents such as sodium carboxymethyl cellulose, optical brighteners, dyes, germicidal agents, suds depressants, suds boosters, peroxy compounds, perfume and alkalinity agents such as NaOH, sodium carbonate or trisodium orthophosphate.
- the enzymes attached to the spray-dried granules can be any of the catalytically active protein materials which are generally found in powdered form. Suitable enzymes degrade or alter one or more types or stains encountered in laundering situations so as to remove the soil or stain from the fabric being laundered or to make the soil or stain more removable by other detergent components. Both degradation and alteration improve soil removability.
- hydrolases degrade soil to remove it or make it more removable.
- the transferases and isomerases alter soil so as to make it more removable.
- the hydrolases are particularly preferred.
- the hydrolases catalyze the addition of water to the substrate, i.e., the substance such as soil with which they interact, and thus, generally cause a breakdown or degradation of such a substrate.
- This breakdown of the substrate is particularly valuable in the ordinary washing procedures, as the substrate and the soil adhering to said substrate is loosened and thus more easily removed.
- the hydrolases are the most important and most preferred sub-class of enzymes for use in cleaning applications.
- Particularly preferred hydrolases are the proteases, esterases, carbohydrases and nucleases, with the protease having the broadest range of soil degradation capability.
- protease catalyze the hydrolysis of the peptide linkage of proteins, polypeptides and related compounds to free amino and carboxyl groups and thus break down the protein structure in soil.
- proteases suitable for use in this invention are pepsin, trypsin, chymotrypsin, collagenase, keratinase, elastase, subtilisin, BPN, papain, bromelin, carboxy peptidase A and B, amino peptidase, aspergillopeptidase A and aspergillopeptidase B.
- Preferred protease are serine proteases which are active in the neutral to alkaline pH range and one produced from microorganisms such as bacteria, fungi or mold.
- Esterases catalyze the hydrolysis of an ester, such as lipid soil, to an acid and an alcohol.
- esterases are gastric lipase, pancreatic lipase, plant lipases, phospholipases, cholinesterases and phosphotases.
- Eterases function primarily in acid systems.
- Carbohydrases catalyze the breakdown of carbohydrate soil.
- Specific examples of this class of enzymes are maltase, saccharase, amylases, cellulase, pectinase, lysozyme, a-glycosidase and ,B-glycosidase. They function primarily in acid to neutral systems.
- the nucleases catalyze the breakdown of nucleic acids and related compounds, degrading residual cell soil such as skin flakes.
- Two specific examples of this subgroup are ribonuclease and desoxyribonuclease.
- the enzymes utilized in the process of this invention are generally obtained and stored in a dry, powdered form.
- the dry, powdered form is most easily handled and generally is more stable than enzymes in a water slurry.
- Enzymes per se have molecular diameters of from about 30 angstroms to several thousand angstroms. However, particle diameters of enzyme powder are normally much larger due to agglomeration of individual enzyme molecules or addition of inert vehicles such as organic clays, sodium or calcium sulfate or sodium chloride, during enzyme manufacture. Enzymes are grown in solution. Such vehicles are added after filtration of such solution to precipitate the enzyme in fine form which is then dried; calcium salts also stabilize enzymes.
- Enzyme powders used in this invention mostly are fine enough to pass through a Tyler Standard 20 mesh screen (0.85 mm.), although larger agglomerates are often found. Some particles of commercially available enzyme powders are fine enough to pass through a Tyler Standard mesh screen. Generally a major amount of particles will remain on a mesh screen. Thus, the powdered enzymes utilized herein usually range in size from about 1 mm. to 1 micron, and most generally from 0.1 mm. to 0.01 mm. The enzyme powders of the examples have a particle size in these ranges.
- Commercial powdered enzyme products are useful and are generally dry powdered products comprised of about 2% to about 80% active enzymes in combination with an inert powdered vehicle such as sodium or calcium sulfate or sodium chloride, clay or starch as the remaining 98-20%.
- Specific active enzyme content of a commercial product is a result of manufacturing methods employed and is not critical herein so long as the resulting detergent granules have the desired enzymatic activity. Pure crystalline enzyme powder can also be employed.
- Many of the commercial enzyme products contain the preferred proteases as the active enzyme. In most cases, a subtilisin comprises the major portion of the proteases: other examples of hydrolases generally included in commercial products are lipases, carbohydrases, esterases and nucleases.
- An enzyme product preferred for use in the detergent compositions of this invention is a proteolytic enzyme, a serine protease, with the trade name of Alcalase, Alcalase has been described as a proteolytic enzyme preparation manufactured by submerged fermentation of a special strain of Bacillus subtilz's.
- the primary enzyme component of Alcalase is subtilisin.
- Alcalase is a fine grayish powder having a crystalline active enzyme content of about 6% and a particle size ranging from 1.2 mm. to .01 mm. and smaller, about 75% passing through a 100 mesh Tyler screen.
- the remainder of the powder is comprised primarily of sodium chloride, calcium sulfate and various inert organic vehicle materials.
- PronaseP, Pronase-AS and Pronase-AF are powdered enzyme products which can also be used to advantage in this invention. These enzymes are produced from the culture broth used for streptomycin manufacture. They are isolated by the successive resin column treatment. The major component of the Pronases is a neutral Streptomyces griseus protease. This enzyme product contains a calcium stabilizer salt.
- CRD-Protease is reported to be obtained by mutation of a Bacillus subtilis organism. Its proteolytic content is about 80% neutral protease and 20% alkaline protease. It contains some amylase. The neutral protease has a molecular weight of about 44,000 and contains from 1 to 2 atoms of zinc per molecule. Its particle size ranges from 0.03 mm. to 0.1 mm.
- the particular enzyme chosen for use in the process of this invention depends on the composition pH, use pH, use temperature and soil types to be degraded or altered.
- the enzyme can be chosen to provide optimum activity and/or stability for any given set of utility conditions. Enzymes active in the pH range of 7-11 are used. Most readily available and suitable are those active in the 8-10 pH range.
- the powdered enzymes are attached to the spray-dried granular detergent in the process of this invention to provide an active enzyme content ranging from about 0.001% to 2%, generally 0.005% to 0.5% of the spraydried detergent granules.
- the amount of enzyme products (enzyme+vehicle) attached to the granular carrier can range up to 20%, of the weight of spray dried granules.
- the organic liquid vehicle with which the powdered enzyme is slurried is an organic, low-boiling solvent which is pure enough to leave no undesirable residue upon evaporation.
- the solvent should have a boiling point within the range of about 55 to about 110 C. so as to be liquid and easily handled at ambient temperatures (65 F.100 F.) or below and to evaporate readily after application to the granules.
- Any of the many well-known organic liquids having the above characteristics are suitable for use in the process of this invention.
- Such liquids should have evaporation rates no faster than that of acetone and no slower than that of isopropanol (rates ranging from 110 to 1160). See the tables in the Kirk Othmer Encyclopedia of Chemical Technology, volume 12, pp. 666*7 et seq.
- suitable solvents are: lower monohydric alcohols such as methanol, ethanol, propanol, isopropanol and isobutanol; lower ketones such as acetone and methyl ethyl ketones; lower alkane hydrocarbons such as hexane and heptane; halogenated alkanes such as ethylene dichloride; aromatic hydrocarbons such as benzene and toluene.
- Organic liquids such as ether, Freons, and petane are too volatile.
- Organic liquids such as phenol, cyclohexanol, octane, butanol, dimethyl sulfoxide and dimethyl formamide, have boiling points which are too high.
- the suitable organic liquids can tolerate up to 10%, preferably no more than 5%, water without losing their non-aqueous characteristics and their suitability for use herein. Preferably they are used in an anhydrous state.
- the slurry of enzyme plus organic liquid should be prepared and used at ambient temperatures or below (e.g. in the range of 40100 F.) in order to avoid any tendency to denature the enzyme.
- the solubility of enzymes in the organic liquids suitable for use in the process of this invention is quite low.
- the powdered diluents with which the enzymes are associated also have a low solubility in the organic liquid.
- These vehicles are relatively safe to handle; they are fluid; they are non-reactive with the enzyme, they are easily sprayed and evaporate readily, resulting in firm even attachment of the enzyme to the spray-dried granules.
- they are suitable vehicles for perfume if it is desired to add enzyme along with an effective amount of perfume to the finished spray-dried granules in the same spray-on step.
- Perfume must be added to spray-dried granules after they are relatively cool because perfume would be degraded and/or wasted by application to hot granules. Ethanol is preferred because it is easily handled and evaporates readily.
- the organic liquid vehicle employed to slurry the enzyme and sprayed on to the spray-dried granules softens or dissolves a small amount of the organic detergent compound in the granules.
- This softened or dissolved detergent compound then associated with the enzyme, at least partially encapsulating it after the organic liquid evaporates.
- Such encapsulation help protect the enzyme and also provides a stronger adherence of the enzyme to the spray-dried granule.
- the powdered enzyme or enzyme product is slurried uniformly with the organic liquid vehicle, preferably at ambient temperatures.
- the proportion of vehicle to enzyme should be at least about 1:1 and can range up to 15, preferably 10, parts liquid vehicle to each part enzyme powder.
- Sufficient vehicle should be used to make the slurry fluid, pumpable and sprayable.
- Organic liquid vehicle substantially in excess of the amount needed to make a fluid slurry is wasteful and creates problems in handling the vapors resulting from evaporation thereof.
- the slurry of enzyme powder and organic liquid vehicle is sprayed on to the spray-dried granules while the granules are in an agitated dispersed state, preferably flowing in a moving stream of air.
- a preferred point of application is at or near the top of the usual air lift, beside a spray tower, in which the spray-dried granules are cooled and dried. Often at the top of this air lift is a fines separator which is an especially convenient place to spray on the slurry of enzyme and organic liquid vehicle. Other methods of spray-on can be employed.
- granules can be conveyed and cooled from the bottom of the tower, e.g., on a conveyor belt, and then introduced into a tumble drum where the spray-on of enzyme-i-vehicle can be affected. After the spray-on by any means, the organic vehicle readily evaporates into 7 the atmosphere. Special attention to such evaporation is not necessary, although venting fans for finished product bins or other containers are desirable.
- Spray dried detergent granules are. prepared in a spray tower by slurrying the following detergent ingredients in a crutcher at 180 F. with suflicient water (about 40%) to make a pumpable sprayable slurry then spray drying the slurry through nozzles in the spray tower.
- the tower contains countercurrent flowing air heated to 600 F. at the inlets and exiting from the tower at 190 F.
- the granules are spray dried to the composition as shown below having an average particle size of about 0.5 mm. and a bulk density of about 0.3 gm./cc.
- Percent Anionic organic synthetic detergent consisting of sodium linear dodecyl benzene sulfonateand sodium tallow alkyl sulfate in 55:45 ratio 17.3
- the 10% water in the granules is mostly in the form of water of hydration in the sodium tripolyphosphate; the free moisture in the granules is about 2% in the exit tube of the fines separator at the top of the air lift.
- the granules temperature in the exit tube is about 120 F.
- a slurry of enzyme powder in ethanol is uniformly sprayed on to the spray dried granules which are flowing in an agitated dispersed state; The spray is directed into the exit tube using a pumping pressure of 80 p.s.i. and a standard spray nozzle.
- the enzyme powder in the slurry is Alcalase (defined above). This slurry is at room temperature and comprises one part Alcalase.
- the ethanol is denatured with methanol.
- Sulficient enzyme slurry is sprayed on to the spray dried granules to provide an Alcalase content of 0.10% content by weight of the detergent composition.
- the alcohol vehicle evaporates quickly from the granules which are sent to finished product storage.
- the pH in water solution of the spray-dried granules is 9.7.
- the enzyme powder is firmly attached to the granules.
- the resulting detergent composition has no segregation disadvantages and retains its enzyme activity for prolonged storage periods. It is an effective laundry detergent with the enzyme content providing significant extra cleaning and soil degrading and soil and stain removal capabilities.
- Example II The process of Example I is repeated again except that the alcohol-Alcalase slurry had a weight ratio of 3 parts ethanol to 1 part Alcalase.
- the enzyme-alcohol slurry is applied at three different levels: one to provide 1% Alcalase in the treated spray-dried granules, another level to provide 0.1% and another level to provide 0.05%.
- These treated spray-dried detergent granules, with firmly attached enzyme are also highly stable and effective laundering agents. They retain their enzymatic activity over prolonged storage periods including storage at higher temperatures.
- Example II The process of Example II is repeated except that the spray-dried granules initially were perfume-free.
- the perfume intended for the granules is admixed with the enzyme-ethanol slurry so as to provide a perfume level in the treated spray-dried granules of 0.11%.
- This enzyme perfume application and the resulting spray-dried granules are quite satisfactory in all respects.
- Substantially similar results can also be obtained by using different formulations for the spray-dried granules.
- Other organic detergents can be used such as: sodium coconut oil soap, the condensation product of 1 mole of coconut fatty alcohol and 6 moles of ethylene oxide; 3 (N,N, dimethyl N dodecylammonio) 2 hydroxypropane-l-sulfonate.
- Other builders can be used in place of the sodium tripolyphosphate, such as tetrasodium pyrophosphate, trisodium nitrilotriacetate, trisodium ethane 1 hydroxy 1,1 diphosphonate or mixtures of any of these. Mixtures of sodium tripolyphosphate and trisodium nitrilotriacetate are very good.
- a process for applying enzymes to spray-dried detergent granules which consist essentially of an organic detergent selected from the group consisting of watersoluble anionic non-soap synthetic detergents, watersoluble non-ionic non-soap synthetic detergents, watersoluble ampholytic non-soap synthetic detergents, watersoluble zwitterionic non-soap synthetic detergents, and fatty acid soaps, an alkaline builder selected from the group consisting of water-soluble inorganic alkaline builder salts, organic alkaline sequestering builder salts, and IniXtures thereof, and sodium silicate comprising the steps of preparing a fluid slurry of enzyme in a liquid, organic vehicle having a boiling point in the range of about 55 C.
- the organic detergent is selected from the group consisting of sulfate an on c non-soap synthetic detergents and sulfonate anlonic non-soap synthetic detergents
- the ratio of detergent to buider ranges from about 2:1 to about 1:10 and the silicate content is from about 3% to 20%
- the organic vehicle is selected from the group consisting of methanol, ethanol, propanol, isopropanol, isobutanol, acetone, methyl ethyl ketones, hexane, heptane, ethylene dichloride, benzene, and toluene.
- silicate in the granules is from 5% to 10% and has an SiO :Na O ratio of from 2.021 to 1.6:1, the detergent and builder together are from 50% to 75% of the granules, the free moisture 2,922,749 1/ 1960 Synder et a1.
- 195-66 content of the granules is less than 2% and the enzyme 3,119,750 1/1964 Faucett et a1.
- 19568 content of the product of the process is from about .001% 3,272,717 9/ 1966 'Fukumoto et al. 195-68 to about 2%. 3,451,935 6/1969 Roald et al. 252135 5.
Landscapes
- Chemical & Material Sciences (AREA)
- Life Sciences & Earth Sciences (AREA)
- Engineering & Computer Science (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Oil, Petroleum & Natural Gas (AREA)
- Wood Science & Technology (AREA)
- Organic Chemistry (AREA)
- Detergent Compositions (AREA)
Abstract
ENZYMES ARE APPLIES TO SPARY-DRIED SILICATE-CONTAINING DETERGENT GRANULES BY SLURRING ENZYME POWDER IN A LIQUID, ORGANIC VEHICLE AND SPRAYING THE SLURRY ONTO THE GRANULES AT A TEMPERATURE BELOW 140*F.
Description
Aug. 17, 1971 B. H. GEDGE lll, ETAL 3,600,319 PROCESS FOR APPLICATION OF ENZYMES TO SPRAY-DRIED DETERGENT GRANULES Filed June 25, 1968 FIN s FINES SEPARATOR OPT ONAL PERFUME CRUTCHER ENZYME FOR VEHICLE DETERGENT SLURRY sLuRRY SPRAY NOZZLE ,L-sPRAY NOZZLE FINISHED PRODUCT AIR LIFT HEATED AIR AIR II\'\//N'l (IRS Burton H. Gedge,111
in, Charles H. Bruin W ISM/d e ATTORNEY United States Patent US. Cl. 252114 6 Claims ABSTRACT OF THE DISCLOSURE 'Enzymes are applied to spray-dried silicate-containing detergent granules by slurrying enzyme powder in a liquid, organic vehicle and spraying the slurry onto the granules at a temperature below 140 F.
This invention relates to a method for applying enzymes to laundry detergent granules from an organic liquid vehicle.
PRIOR ART AND BACKGROUND OF THE INVENTION Laundry products containing enzymes are well known. Enzymes aid in laundering by attacking soil and stains found on soiled fabrics. Soils and stains are decomposed or altered in such an attack so as to render them more removable during laundering. Enzymes are usually used as a component of a laundry detergent formulation containing conventional cleaning ingredients, such as builders and organic detergents. The enzymes suitable for such laundry uses are usually found in a fine powder form. Enzymes are expensive and powerful materials which must be judiciously formulated and used. Such fine powders of concentrated materials are difficult to handle, measure and formulate.
Such prior art, enzyme-containing laundry products are mechanical mixtures of a fine enzyme powder and other granular materials. Enzyme powder in such mechanical mixtures tends to segregate, resulting in a non-uniform product. Non-uniformity results in an undependable product in use. Such mechanical mixtures also present stability problems resulting from the mobility of the enzyme powder in the mixture; it is exposed to some cleaning ingredients and environmental condition which may either attack the enzyme or aid it in degrading itself. For example, moisture tends to cause the enzyme to degrade itself; many enzymes are incompatible with highly alkaline detergent materials such as caustic soda and sodium silicate, particularly in the presence of moisture.
The prior art has taught some very good techniques for applying enzymes to detergent granules to overcome segregation and stability problems. For example, copending, commonly assigned application Ser. No. 630,199 of Roald and De Oude filed Apr. 12, 1967 teaches use of water to attach powdered enzymes to an hydratable granular carrier salt. Copending commonly assigned application of McCarty, Ser. No. 635, 293 filed Apr. 12, 1967, now Pat. No. 3,519,570, teaches the use of nonionic surface active materials to conglutinate powdered enzymes and detergent granules. These techniques, however, are not readily adaptable to the application of powdered enzymes to alkaline, silicate-containing, spray-dried detergent granules With the utilization of existing equipment.
Most granular detergent compositions are spray-dried from a hot, aqueous, alkaline, fluid slurry which contains sodium silicate. The manner of any enzyme addition to such compositions is critical, since the most useful enzymes for detergent compositions are very sensitive to alkalinity in the presence of moisture and to heat. These two environments must be avoided to the maximum pos- 3,000,319 Patented Aug. 17, 197i (1) addition to the hot fluid slurry prior to spray drying;
(2) addition to the tower or at the bottom thereof while the granules are Warm and moisttemperatures within the spray tower usually range from about 600 F. at the air inlet to about 160 F. at the air exit;
(3) addition in the lower part of the airlift where the granules are cooled and dried (the granules are still too warm and the presence of unhydrated moisture would promote an attack on an enzyme by the silicate);
(4) addition, at the top of the air lift or in the fines separator after the granules have cooled, with a spray-on of a water-enzyme slurry (the use of an enzyme-Water slurry would tend to expose the enzyme to an attack bythe high alkalinity in the silicate-containing granules).
SUMMARY OF THE INVENTION Notwithstanding the above problems, it was found that effective application of the enzyme to spray-dried, silicatecontaining detergent granules, after they have been cooled to at least 140 F., preferably 120 F., can be effected by spraying powdered enzyme on to the granules in a slurry of a liquid organic vehicle. Such a vehicle provides a fiuid enzyme slurry suitable for the usual spraying equipment. These liquid vehicles do not degrade the enzyme and they provide an application technique for attaching the enzyme to the spray-dried granules without exposing the enzyme to attack by silicate or other components of the granules. The liquid organic vehicle evaporates after application, leaving an enzyme-containing detergent granule having very good enzyme stability. The enzyme is applied and firmly attached to the granules in a way which is efficient, which can utilize existing equipment, which does not unduly expose the enzyme to the degrading effects of heat and moisture-supported alkalinity and which provides a stable non-segregating product. The application technique of the process of this invention is shown in the schematic drawing which is described in Example I.
DETAILED DESCRIPTION The spray-dried granular detergent composition to which enzymes are applied by the process of this invention consists essentially of an organic detergent, an alkaline builder and sodium silicate. The organic detergent and alkaline builder range in weight ratio from about 2:1 to about 1:10, preferably 1:2 to 1:6. Together they comprise about 40% to about 97%, preferably 50% to of the spray-dried granules. These granules contain from about 3% to about 20%, preferably 5% to 10%, sodium silicate having a SiO zNa O ratio ranging from about 3.621 to about 1:1, preferably from 2.011 to 16:1. The granules have a pH in water solution of about 9 to 12, generally 9.5 to 11.5. The granules range in particle size from about .075 mm. to about 3.33 mm. (through 6 mesh and on 200 mesh-Tyler standard screens), preferably from 0.2 mm. to 2 mm. They range in density from about 0.2 gram/cc. to about 0.8 gram/cc.
At the time the enzyme slurry is sprayed on, the granules should have a free moisture content of less than 5% and preferably less than 2% in order to reduce attack on the enzyme by the silicate. Free moisture is moisture other than water of hydration in the granular components.
When the builder in the granules is sodium tripolyphosphate or other hydratable builder salt, free moisture often continues in the state of being taken up as water of hydration for a period after spray drying. This taking up continues even after the enzyme application, often to the point of free moisture. Generally there is a reserve of hydration capacity, such that exposure of the granules to additional free moisture (from sources other than the initial detergent slurry which is spray-dried) does not result in undue attack on the enzyme by the alkalinity in the granule. Such additional free moisture is taken up as water of hydration and is therefore not readily available to stimulate an attack on the enzyme by the silicate alkalinity.
The organic detergent compounds used in the spraydried granular detergent used in this invention are of the usual water-soluble anionic non-soap, nonionic, ampholytic and zwitterionic synthetic detergent classes or fatty acid soap. Of these, the anionic non-soap synthetic class, in the form of their alkali metal salts, are preferred. This class is usually characterized as organic sulfuric reaction products having in their molecular structure an alkyl radical containing from 8-22 carbon atoms and a sulfonic acid or sulfuric acid ester radical. This class is preferred because it is more readily spray dried than the other and has the best detergency characteristics. All of the above subclasses are described in additional detail in US. Pat. 3,351,558 issued to Roger E. Zimmerer Nov. 7, 1967, particularly from line 59, column 6 to line 74, column 9. This description is incorporated herein by reference.
The alkaline builders of the spray-dried detergent granules are of the usual classes, both inorganic and organic. The preferred classes of alkaline builder salts are the water-soluble alkali metal polyphosphates, aminopolyacetates, polyphosphonates and polycarboxylates. Representative examples of builder compounds of these classes are as follows: sodium tripolyphosphate, sodium pyrophosphate, sodium ethylenediaminetetraacetate, sodium nitrilotriacetate, sodium ethane hydroxy diphosphonate, sodium ethane-l-hydroxy-l,1,2-triphosphonate, and the polycarboxylates described in the patent of Francis L. Diehl, US. 3,308,067, issued Mar. 7, 1967. Other examples of suitable builders can be found in Zimmerers US. Pat. 3,351,- 558, especially from line 64, column 2 to line 38, column 3 which is incorporated herein by reference.
The spray-dried detergent granules can contain any of the other usual optional additives for such products including any of the following: inorganic fillers such as sodium sulfate in an amount up to about 35%; effective amounts of soil suspending agents such as sodium carboxymethyl cellulose, optical brighteners, dyes, germicidal agents, suds depressants, suds boosters, peroxy compounds, perfume and alkalinity agents such as NaOH, sodium carbonate or trisodium orthophosphate.
The enzymes attached to the spray-dried granules can be any of the catalytically active protein materials which are generally found in powdered form. Suitable enzymes degrade or alter one or more types or stains encountered in laundering situations so as to remove the soil or stain from the fabric being laundered or to make the soil or stain more removable by other detergent components. Both degradation and alteration improve soil removability.
The hydrolases, hydrases, oxidoreductases and desmolases degrade soil to remove it or make it more removable. The transferases and isomerases alter soil so as to make it more removable. Of these enzyme classes the hydrolases are particularly preferred.
The hydrolases catalyze the addition of water to the substrate, i.e., the substance such as soil with which they interact, and thus, generally cause a breakdown or degradation of such a substrate. This breakdown of the substrate is particularly valuable in the ordinary washing procedures, as the substrate and the soil adhering to said substrate is loosened and thus more easily removed. For this reason, the hydrolases are the most important and most preferred sub-class of enzymes for use in cleaning applications. Particularly preferred hydrolases are the proteases, esterases, carbohydrases and nucleases, with the protease having the broadest range of soil degradation capability.
The protease catalyze the hydrolysis of the peptide linkage of proteins, polypeptides and related compounds to free amino and carboxyl groups and thus break down the protein structure in soil. Specific examples of proteases suitable for use in this invention are pepsin, trypsin, chymotrypsin, collagenase, keratinase, elastase, subtilisin, BPN, papain, bromelin, carboxy peptidase A and B, amino peptidase, aspergillopeptidase A and aspergillopeptidase B. Preferred protease are serine proteases which are active in the neutral to alkaline pH range and one produced from microorganisms such as bacteria, fungi or mold. The serine proteases which are procured by mammalian systems. e.g., pancreatin, are useful in acid situations.
Esterases catalyze the hydrolysis of an ester, such as lipid soil, to an acid and an alcohol. Specific examples of the esterases are gastric lipase, pancreatic lipase, plant lipases, phospholipases, cholinesterases and phosphotases. Eterases function primarily in acid systems.
Carbohydrases catalyze the breakdown of carbohydrate soil. Specific examples of this class of enzymes are maltase, saccharase, amylases, cellulase, pectinase, lysozyme, a-glycosidase and ,B-glycosidase. They function primarily in acid to neutral systems.
The nucleases catalyze the breakdown of nucleic acids and related compounds, degrading residual cell soil such as skin flakes. Two specific examples of this subgroup are ribonuclease and desoxyribonuclease.
The enzymes utilized in the process of this invention are generally obtained and stored in a dry, powdered form. The dry, powdered form is most easily handled and generally is more stable than enzymes in a water slurry. Enzymes per se have molecular diameters of from about 30 angstroms to several thousand angstroms. However, particle diameters of enzyme powder are normally much larger due to agglomeration of individual enzyme molecules or addition of inert vehicles such as organic clays, sodium or calcium sulfate or sodium chloride, during enzyme manufacture. Enzymes are grown in solution. Such vehicles are added after filtration of such solution to precipitate the enzyme in fine form which is then dried; calcium salts also stabilize enzymes. Enzyme powders used in this invention mostly are fine enough to pass through a Tyler Standard 20 mesh screen (0.85 mm.), although larger agglomerates are often found. Some particles of commercially available enzyme powders are fine enough to pass through a Tyler Standard mesh screen. Generally a major amount of particles will remain on a mesh screen. Thus, the powdered enzymes utilized herein usually range in size from about 1 mm. to 1 micron, and most generally from 0.1 mm. to 0.01 mm. The enzyme powders of the examples have a particle size in these ranges.
Commercial powdered enzyme products are useful and are generally dry powdered products comprised of about 2% to about 80% active enzymes in combination with an inert powdered vehicle such as sodium or calcium sulfate or sodium chloride, clay or starch as the remaining 98-20%. Specific active enzyme content of a commercial product is a result of manufacturing methods employed and is not critical herein so long as the resulting detergent granules have the desired enzymatic activity. Pure crystalline enzyme powder can also be employed. Many of the commercial enzyme products contain the preferred proteases as the active enzyme. In most cases, a subtilisin comprises the major portion of the proteases: other examples of hydrolases generally included in commercial products are lipases, carbohydrases, esterases and nucleases.
Specific examples of commercial enzyme products and the manufacture thereof include: Alcalase, Novo Industri, Maxatase, Koninklijke Nederlandsche Gist En Spiritusfabriek N.V., Protease B-4000- and Protease AP, Schweizerische Ferment A.G., CRD-Protease, Monsanto Company, Viokase, Viobin Corporation, Pronase-P, Pronase-AS and Pronase-AF, Koken Chemical Company, Japan; Rapidase P-2000, Rapid'ase, France; Takamine, Bromelain 1:10, HT proteolytic enzyme 200, Enzyme L-W (derived from fungi rather than bacteria), Miles Chemical Company, Rhozym P11 concentrate, Pectinol, Lipase B, Rhozyme PF, Rhozyme I-25, Rohm and Haas, Rhozyme PF and J-35 have salt and corn starch vehicles and are proteases having diastase activity; Amprozyme 200, Jacques Wolf & Company.
An enzyme product preferred for use in the detergent compositions of this invention is a proteolytic enzyme, a serine protease, with the trade name of Alcalase, Alcalase has been described as a proteolytic enzyme preparation manufactured by submerged fermentation of a special strain of Bacillus subtilz's. The primary enzyme component of Alcalase is subtilisin. Alcalase is a fine grayish powder having a crystalline active enzyme content of about 6% and a particle size ranging from 1.2 mm. to .01 mm. and smaller, about 75% passing through a 100 mesh Tyler screen. The remainder of the powder is comprised primarily of sodium chloride, calcium sulfate and various inert organic vehicle materials.
PronaseP, Pronase-AS and Pronase-AF are powdered enzyme products which can also be used to advantage in this invention. These enzymes are produced from the culture broth used for streptomycin manufacture. They are isolated by the successive resin column treatment. The major component of the Pronases is a neutral Streptomyces griseus protease. This enzyme product contains a calcium stabilizer salt.
CRD-Protease is reported to be obtained by mutation of a Bacillus subtilis organism. Its proteolytic content is about 80% neutral protease and 20% alkaline protease. It contains some amylase. The neutral protease has a molecular weight of about 44,000 and contains from 1 to 2 atoms of zinc per molecule. Its particle size ranges from 0.03 mm. to 0.1 mm.
The particular enzyme chosen for use in the process of this invention depends on the composition pH, use pH, use temperature and soil types to be degraded or altered. The enzyme can be chosen to provide optimum activity and/or stability for any given set of utility conditions. Enzymes active in the pH range of 7-11 are used. Most readily available and suitable are those active in the 8-10 pH range.
The powdered enzymes are attached to the spray-dried granular detergent in the process of this invention to provide an active enzyme content ranging from about 0.001% to 2%, generally 0.005% to 0.5% of the spraydried detergent granules. Taking into account inert vehicles in commercial powdered enzyme products, the amount of enzyme products (enzyme+vehicle) attached to the granular carrier can range up to 20%, of the weight of spray dried granules.
The organic liquid vehicle with which the powdered enzyme is slurried is an organic, low-boiling solvent which is pure enough to leave no undesirable residue upon evaporation. The solvent should have a boiling point within the range of about 55 to about 110 C. so as to be liquid and easily handled at ambient temperatures (65 F.100 F.) or below and to evaporate readily after application to the granules. Any of the many well-known organic liquids having the above characteristics are suitable for use in the process of this invention. Such liquids should have evaporation rates no faster than that of acetone and no slower than that of isopropanol (rates ranging from 110 to 1160). See the tables in the Kirk Othmer Encyclopedia of Chemical Technology, volume 12, pp. 666*7 et seq. (1954), incorporated herein by reference. Specific examples of such suitable solvents are: lower monohydric alcohols such as methanol, ethanol, propanol, isopropanol and isobutanol; lower ketones such as acetone and methyl ethyl ketones; lower alkane hydrocarbons such as hexane and heptane; halogenated alkanes such as ethylene dichloride; aromatic hydrocarbons such as benzene and toluene. Organic liquids such as ether, Freons, and petane are too volatile. Organic liquids such as phenol, cyclohexanol, octane, butanol, dimethyl sulfoxide and dimethyl formamide, have boiling points which are too high. The suitable organic liquids can tolerate up to 10%, preferably no more than 5%, water without losing their non-aqueous characteristics and their suitability for use herein. Preferably they are used in an anhydrous state. The slurry of enzyme plus organic liquid should be prepared and used at ambient temperatures or below (e.g. in the range of 40100 F.) in order to avoid any tendency to denature the enzyme. The solubility of enzymes in the organic liquids suitable for use in the process of this invention is quite low. The powdered diluents with which the enzymes are associated also have a low solubility in the organic liquid.
These vehicles are relatively safe to handle; they are fluid; they are non-reactive with the enzyme, they are easily sprayed and evaporate readily, resulting in firm even attachment of the enzyme to the spray-dried granules. Moreover, they are suitable vehicles for perfume if it is desired to add enzyme along with an effective amount of perfume to the finished spray-dried granules in the same spray-on step. Perfume must be added to spray-dried granules after they are relatively cool because perfume would be degraded and/or wasted by application to hot granules. Ethanol is preferred because it is easily handled and evaporates readily.
While it is desired not to be bound by theory it is believed that the organic liquid vehicle employed to slurry the enzyme and sprayed on to the spray-dried granules softens or dissolves a small amount of the organic detergent compound in the granules. This softened or dissolved detergent compound then associated with the enzyme, at least partially encapsulating it after the organic liquid evaporates. Such encapsulation help protect the enzyme and also provides a stronger adherence of the enzyme to the spray-dried granule.
In practicing the process of this invention the powdered enzyme or enzyme product (enzyme plus powdered vehicle) is slurried uniformly with the organic liquid vehicle, preferably at ambient temperatures. The proportion of vehicle to enzyme should be at least about 1:1 and can range up to 15, preferably 10, parts liquid vehicle to each part enzyme powder. Sufficient vehicle should be used to make the slurry fluid, pumpable and sprayable. Organic liquid vehicle substantially in excess of the amount needed to make a fluid slurry is wasteful and creates problems in handling the vapors resulting from evaporation thereof.
The slurry of enzyme powder and organic liquid vehicle is sprayed on to the spray-dried granules while the granules are in an agitated dispersed state, preferably flowing in a moving stream of air. A preferred point of application is at or near the top of the usual air lift, beside a spray tower, in which the spray-dried granules are cooled and dried. Often at the top of this air lift is a fines separator which is an especially convenient place to spray on the slurry of enzyme and organic liquid vehicle. Other methods of spray-on can be employed. so long as the above described conditions are observed and can include the following: granules can be conveyed and cooled from the bottom of the tower, e.g., on a conveyor belt, and then introduced into a tumble drum where the spray-on of enzyme-i-vehicle can be affected. After the spray-on by any means, the organic vehicle readily evaporates into 7 the atmosphere. Special attention to such evaporation is not necessary, although venting fans for finished product bins or other containers are desirable.
The process of this invention is illustrated with the examples which follow. The process is that illustrated in the drawing which shows schematically the apparatus arrangement employed. Examples are not to be regarded as limiting the invention. All amounts and percentages and ratios in the specification, examples and claims are by weight unless otherwise indicated.
EXAMPLE I Spray dried detergent granules are. prepared in a spray tower by slurrying the following detergent ingredients in a crutcher at 180 F. with suflicient water (about 40%) to make a pumpable sprayable slurry then spray drying the slurry through nozzles in the spray tower. The tower contains countercurrent flowing air heated to 600 F. at the inlets and exiting from the tower at 190 F. The granules are spray dried to the composition as shown below having an average particle size of about 0.5 mm. and a bulk density of about 0.3 gm./cc.
Percent Anionic organic synthetic detergent consisting of sodium linear dodecyl benzene sulfonateand sodium tallow alkyl sulfate in 55:45 ratio 17.3
Monoethanolamide of coconut fatty acid 2.3 Sodium tripolyphosphate 50 Sodium silicate (SiO :Na O ratio of 1.6:1) 6 Sodium carboxymethyl cellulose 0.3 Sodium sulfate 13.9 Perfume 0.13 Water 10 Brighteners .07
The 10% water in the granules is mostly in the form of water of hydration in the sodium tripolyphosphate; the free moisture in the granules is about 2% in the exit tube of the fines separator at the top of the air lift. The granules temperature in the exit tube is about 120 F. At the exit tube of the fines separator, a slurry of enzyme powder in ethanol is uniformly sprayed on to the spray dried granules which are flowing in an agitated dispersed state; The spray is directed into the exit tube using a pumping pressure of 80 p.s.i. and a standard spray nozzle. The enzyme powder in the slurry is Alcalase (defined above). This slurry is at room temperature and comprises one part Alcalase. and 9 parts ethanol. The ethanol is denatured with methanol. Sulficient enzyme slurry is sprayed on to the spray dried granules to provide an Alcalase content of 0.10% content by weight of the detergent composition. The alcohol vehicle evaporates quickly from the granules which are sent to finished product storage.
The pH in water solution of the spray-dried granules is 9.7. The enzyme powder is firmly attached to the granules. The resulting detergent composition has no segregation disadvantages and retains its enzyme activity for prolonged storage periods. It is an effective laundry detergent with the enzyme content providing significant extra cleaning and soil degrading and soil and stain removal capabilities.
The process of this example is repeated to achieve an Alcalase content of 0.05% in the granular detergent, instead of 0.10%, with substantially equivalent results except with a lower level of enzymatic activity.
EXAMPLE II The process of Example I is repeated again except that the alcohol-Alcalase slurry had a weight ratio of 3 parts ethanol to 1 part Alcalase. The enzyme-alcohol slurry is applied at three different levels: one to provide 1% Alcalase in the treated spray-dried granules, another level to provide 0.1% and another level to provide 0.05%. These treated spray-dried detergent granules, with firmly attached enzyme, are also highly stable and effective laundering agents. They retain their enzymatic activity over prolonged storage periods including storage at higher temperatures.
The process of Example II is repeated except that the spray-dried granules initially were perfume-free. The perfume intended for the granules is admixed with the enzyme-ethanol slurry so as to provide a perfume level in the treated spray-dried granules of 0.11%. This enzyme perfume application and the resulting spray-dried granules are quite satisfactory in all respects.
Substantially equivalent results can be obtained in the above examples employing any of the many powdered enzymes having soil removal or soil and stain degradation capabilities. Likewise substantially similar results can be obtained by using other organic liquid vehicles instead of ethanol, such as methanol, propanol, isopropanol, benzene, hexane or acetone.
Substantially similar results can also be obtained by using different formulations for the spray-dried granules. Other organic detergents can be used such as: sodium coconut oil soap, the condensation product of 1 mole of coconut fatty alcohol and 6 moles of ethylene oxide; 3 (N,N, dimethyl N dodecylammonio) 2 hydroxypropane-l-sulfonate. Other builders can be used in place of the sodium tripolyphosphate, such as tetrasodium pyrophosphate, trisodium nitrilotriacetate, trisodium ethane 1 hydroxy 1,1 diphosphonate or mixtures of any of these. Mixtures of sodium tripolyphosphate and trisodium nitrilotriacetate are very good.
The foregoing description of the invention has been presented describing certain preferred embodiments. It is not intended that the invention should be limited thereto since variations and modifications thereof will be obvious to those skilled in the art, all of which are within the spirit and scope of this invention.
What is claimed is:
1. A process for applying enzymes to spray-dried detergent granules which consist essentially of an organic detergent selected from the group consisting of watersoluble anionic non-soap synthetic detergents, watersoluble non-ionic non-soap synthetic detergents, watersoluble ampholytic non-soap synthetic detergents, watersoluble zwitterionic non-soap synthetic detergents, and fatty acid soaps, an alkaline builder selected from the group consisting of water-soluble inorganic alkaline builder salts, organic alkaline sequestering builder salts, and IniXtures thereof, and sodium silicate comprising the steps of preparing a fluid slurry of enzyme in a liquid, organic vehicle having a boiling point in the range of about 55 C. to about C., an evaporation rate in the range of about 110 to about 1160, and selected from the group consisting of lower monohydric alcohols, lower ketones, lower alkane hydrocarbons, halogenated alkanes, and aromatic hydrocarbons, and spraying said slurry onto said granules which are at a temperature of less than about 140 F. and have less than 5% free moisture.
2. The process of claim 1 wherein the organic detergent is selected from the group consisting of sulfate an on c non-soap synthetic detergents and sulfonate anlonic non-soap synthetic detergents, the ratio of detergent to buider ranges from about 2:1 to about 1:10 and the silicate content is from about 3% to 20%, and the organic vehicle is selected from the group consisting of methanol, ethanol, propanol, isopropanol, isobutanol, acetone, methyl ethyl ketones, hexane, heptane, ethylene dichloride, benzene, and toluene.
3. The process of claim 2 wherein the vehicle is ethanol, the enzyme consists essentially of protease, the ratio of vehicle to enzyme is at least about 1:1 and the temperature is less than F., and the said ratio ranges from 1:2to 1:6.
4. The process of claim 3 wherein the silicate in the granules is from 5% to 10% and has an SiO :Na O ratio of from 2.021 to 1.6:1, the detergent and builder together are from 50% to 75% of the granules, the free moisture 2,922,749 1/ 1960 Synder et a1. 195-66 content of the granules is less than 2% and the enzyme 3,119,750 1/1964 Faucett et a1. 19568 content of the product of the process is from about .001% 3,272,717 9/ 1966 'Fukumoto et al. 195-68 to about 2%. 3,451,935 6/1969 Roald et al. 252135 5. The process of claim 4 wherein perfume is included 5 in the said slurry. LEON D. ROSDOL, Primary Examiner 6. The product of the process of claim 4. WILLIS, Assistant Examiner References Cited US CL UNITED STATES PATENTS z52-137,13s, 139, 152,153,161
2,763,618 9/1956 Hendrix 252--153 ter 0% Gamble Company.
Hereby dedicates to the Public the entire remaining term of said patent.
[Ofiicial Gazette Febmary 29, 1.972.]
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US73982768A | 1968-06-25 | 1968-06-25 |
Publications (1)
Publication Number | Publication Date |
---|---|
US3600319A true US3600319A (en) | 1971-08-17 |
Family
ID=24973939
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
US739827A Expired - Lifetime US3600319A (en) | 1968-06-25 | 1968-06-25 | Process for application of enzymes to spray-dried detergent granules |
Country Status (1)
Country | Link |
---|---|
US (1) | US3600319A (en) |
Cited By (46)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US3860536A (en) * | 1970-01-02 | 1975-01-14 | Cpc International Inc | Enzyme-detergent combination |
US3882034A (en) * | 1969-12-15 | 1975-05-06 | Colgate Palmolive Co | Simultaneous formation of expanding borax particles and spray dried detergents |
US4131558A (en) * | 1975-02-14 | 1978-12-26 | The Procter & Gamble Company | Process for preparing an orthophosphate-silicate detergent product |
US4404128A (en) * | 1981-05-29 | 1983-09-13 | The Procter & Gamble Company | Enzyme detergent composition |
US4711739A (en) * | 1986-12-18 | 1987-12-08 | S. C. Johnson & Son, Inc. | Enzyme prespotter composition stabilized with water insoluble polyester or polyether polyol |
DE3704465A1 (en) * | 1987-02-13 | 1988-08-25 | Roehm Gmbh | LIQUID FORMULATIONS OF ENZYMES |
EP0693549A1 (en) | 1994-07-19 | 1996-01-24 | The Procter & Gamble Company | Solid bleach activator compositions |
EP0753557A1 (en) | 1995-07-13 | 1997-01-15 | The Procter & Gamble Company | Packaged foaming composition |
EP0753567A1 (en) | 1995-07-14 | 1997-01-15 | The Procter & Gamble Company | Softening through the wash compositions |
EP0778342A1 (en) | 1995-12-06 | 1997-06-11 | The Procter & Gamble Company | Detergent compositions |
WO1997042282A1 (en) | 1996-05-03 | 1997-11-13 | The Procter & Gamble Company | Detergent compositions comprising polyamine polymers with improved soil dispersancy |
US20040247777A1 (en) * | 2003-06-06 | 2004-12-09 | Ringeisen Bradley R. | Biological laser printing for tissue microdissection via indirect photon-biomaterial interactions |
US20070027053A1 (en) * | 2003-10-16 | 2007-02-01 | Reckitt Benckiser N.V. | Detergent composition comprising coated bleach particle |
WO2011088089A1 (en) | 2010-01-12 | 2011-07-21 | The Procter & Gamble Company | Intermediates and surfactants useful in household cleaning and personal care compositions, and methods of making the same |
WO2012003316A1 (en) | 2010-07-02 | 2012-01-05 | The Procter & Gamble Company | Process for making films from nonwoven webs |
WO2012003367A2 (en) | 2010-07-02 | 2012-01-05 | The Procter & Gamble Company | Method for delivering an active agent |
WO2012003351A2 (en) | 2010-07-02 | 2012-01-05 | The Procter & Gamble Company | Web material and method for making same |
WO2012003319A2 (en) | 2010-07-02 | 2012-01-05 | The Procter & Gamble Company | Filaments comprising an active agent nonwoven webs and methods for making same |
WO2012003300A2 (en) | 2010-07-02 | 2012-01-05 | The Procter & Gamble Company | Filaments comprising a non-perfume active agent nonwoven webs and methods for making same |
WO2012009660A2 (en) | 2010-07-15 | 2012-01-19 | The Procter & Gamble Company | Detergent compositions comprising microbially produced fatty alcohols and derivatives thereof |
WO2012009525A2 (en) | 2010-07-15 | 2012-01-19 | The Procter & Gamble Company | Compositions comprising a near terminal-branched compound and methods of making the same |
WO2012112828A1 (en) | 2011-02-17 | 2012-08-23 | The Procter & Gamble Company | Bio-based linear alkylphenyl sulfonates |
WO2012138423A1 (en) | 2011-02-17 | 2012-10-11 | The Procter & Gamble Company | Compositions comprising mixtures of c10-c13 alkylphenyl sulfonates |
WO2013002786A1 (en) | 2011-06-29 | 2013-01-03 | Solae | Baked food compositions comprising soy whey proteins that have been isolated from processing streams |
WO2013043805A1 (en) | 2011-09-20 | 2013-03-28 | The Procter & Gamble Company | Detergent compositions comprising primary surfactant systems comprising highly branched surfactants especially isoprenoid - based surfactants |
WO2013043852A2 (en) | 2011-09-20 | 2013-03-28 | The Procter & Gamble Company | Easy-rinse detergent compositions comprising isoprenoid-based surfactants |
WO2013043855A2 (en) | 2011-09-20 | 2013-03-28 | The Procter & Gamble Company | High suds detergent compositions comprising isoprenoid-based surfactants |
WO2013043803A2 (en) | 2011-09-20 | 2013-03-28 | The Procter & Gamble Company | Detergent compositions comprising specific blend ratios of isoprenoid-based surfactants |
WO2013043857A1 (en) | 2011-09-20 | 2013-03-28 | The Procter & Gamble Company | Detergent compositions comprising sustainable surfactant systems comprising isoprenoid-derived surfactants |
WO2013070559A1 (en) | 2011-11-11 | 2013-05-16 | The Procter & Gamble Company | Surface treatment compositions including shielding salts |
FR2985273A1 (en) | 2012-01-04 | 2013-07-05 | Procter & Gamble | FIBROUS STRUCTURES CONTAINING ASSETS AND HAVING MULTIPLE REGIONS |
FR3014456A1 (en) | 2013-12-09 | 2015-06-12 | Procter & Gamble | |
WO2015112671A1 (en) | 2014-01-24 | 2015-07-30 | The Procter & Gamble Company | Consumer product compositions |
CN105059764A (en) * | 2015-07-09 | 2015-11-18 | 滁州市润达溶剂有限公司 | Heptanes liquefaction outflow device |
US9464261B2 (en) | 2010-05-14 | 2016-10-11 | The Sun Products Corporation | Polymer-containing cleaning compositions and methods of production and use thereof |
WO2018140431A1 (en) | 2017-01-27 | 2018-08-02 | The Procter & Gamble Company | Active agent-containing articles that exhibit consumer acceptable article in-use properties |
WO2018140432A1 (en) | 2017-01-27 | 2018-08-02 | The Procter & Gamble Company | Active agent-containing articles that exhibit consumer acceptable article in-use properties |
WO2018140472A1 (en) | 2017-01-27 | 2018-08-02 | The Procter & Gamble Company | Active agent-containing articles that exhibit consumer acceptable article in-use properties |
WO2018140454A1 (en) | 2017-01-27 | 2018-08-02 | The Procter & Gamble Company | Active agent-containing articles and product-shipping assemblies for containing the same |
EP3369845A1 (en) | 2012-01-04 | 2018-09-05 | The Procter & Gamble Company | Active containing fibrous structures with multiple regions having differing densities |
WO2020123889A1 (en) | 2018-12-14 | 2020-06-18 | The Procter & Gamble Company | Foaming fibrous structures comprising particles and methods for making same |
EP3719192A1 (en) | 2012-01-04 | 2020-10-07 | The Procter & Gamble Company | Fibrous structures comprising particles and methods for making same |
WO2021026556A1 (en) | 2019-08-02 | 2021-02-11 | The Procter & Gamble Company | Foaming compositions for producing a stable foam and methods for making same |
WO2021097004A1 (en) | 2019-11-15 | 2021-05-20 | The Procter & Gamble Company | Graphic-containing soluble articles and methods for making same |
WO2022251838A1 (en) | 2021-05-28 | 2022-12-01 | The Procter & Gamble Company | Natural polymer-based fibrous elements comprising a surfactant and methods for making same |
WO2023057367A1 (en) | 2021-10-08 | 2023-04-13 | Unilever Ip Holdings B.V. | Laundry composition |
-
1968
- 1968-06-25 US US739827A patent/US3600319A/en not_active Expired - Lifetime
Cited By (73)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US3882034A (en) * | 1969-12-15 | 1975-05-06 | Colgate Palmolive Co | Simultaneous formation of expanding borax particles and spray dried detergents |
US3860536A (en) * | 1970-01-02 | 1975-01-14 | Cpc International Inc | Enzyme-detergent combination |
US4131558A (en) * | 1975-02-14 | 1978-12-26 | The Procter & Gamble Company | Process for preparing an orthophosphate-silicate detergent product |
US4404128A (en) * | 1981-05-29 | 1983-09-13 | The Procter & Gamble Company | Enzyme detergent composition |
US4711739A (en) * | 1986-12-18 | 1987-12-08 | S. C. Johnson & Son, Inc. | Enzyme prespotter composition stabilized with water insoluble polyester or polyether polyol |
DE3704465A1 (en) * | 1987-02-13 | 1988-08-25 | Roehm Gmbh | LIQUID FORMULATIONS OF ENZYMES |
EP0693549A1 (en) | 1994-07-19 | 1996-01-24 | The Procter & Gamble Company | Solid bleach activator compositions |
EP0753557A1 (en) | 1995-07-13 | 1997-01-15 | The Procter & Gamble Company | Packaged foaming composition |
EP0753567A1 (en) | 1995-07-14 | 1997-01-15 | The Procter & Gamble Company | Softening through the wash compositions |
EP0778342A1 (en) | 1995-12-06 | 1997-06-11 | The Procter & Gamble Company | Detergent compositions |
WO1997042282A1 (en) | 1996-05-03 | 1997-11-13 | The Procter & Gamble Company | Detergent compositions comprising polyamine polymers with improved soil dispersancy |
US20040247777A1 (en) * | 2003-06-06 | 2004-12-09 | Ringeisen Bradley R. | Biological laser printing for tissue microdissection via indirect photon-biomaterial interactions |
US20050018036A1 (en) * | 2003-06-06 | 2005-01-27 | Jason Barron | Biological laser printing via indirect photon-biomaterial interactions |
US7294367B2 (en) * | 2003-06-06 | 2007-11-13 | The United States Of America As Represented By The Secretary Of The Navy | Biological laser printing via indirect photon-biomaterial interactions |
US7381440B2 (en) | 2003-06-06 | 2008-06-03 | The United States Of America As Represented By The Secretary Of The Navy | Biological laser printing for tissue microdissection via indirect photon-biomaterial interactions |
US20070027053A1 (en) * | 2003-10-16 | 2007-02-01 | Reckitt Benckiser N.V. | Detergent composition comprising coated bleach particle |
WO2011088089A1 (en) | 2010-01-12 | 2011-07-21 | The Procter & Gamble Company | Intermediates and surfactants useful in household cleaning and personal care compositions, and methods of making the same |
US8933131B2 (en) | 2010-01-12 | 2015-01-13 | The Procter & Gamble Company | Intermediates and surfactants useful in household cleaning and personal care compositions, and methods of making the same |
US9464261B2 (en) | 2010-05-14 | 2016-10-11 | The Sun Products Corporation | Polymer-containing cleaning compositions and methods of production and use thereof |
WO2012003367A2 (en) | 2010-07-02 | 2012-01-05 | The Procter & Gamble Company | Method for delivering an active agent |
WO2012003351A2 (en) | 2010-07-02 | 2012-01-05 | The Procter & Gamble Company | Web material and method for making same |
WO2012003300A2 (en) | 2010-07-02 | 2012-01-05 | The Procter & Gamble Company | Filaments comprising a non-perfume active agent nonwoven webs and methods for making same |
WO2012003360A2 (en) | 2010-07-02 | 2012-01-05 | The Procter & Gamble Company | Detergent product and method for making same |
WO2012003319A2 (en) | 2010-07-02 | 2012-01-05 | The Procter & Gamble Company | Filaments comprising an active agent nonwoven webs and methods for making same |
WO2012003316A1 (en) | 2010-07-02 | 2012-01-05 | The Procter & Gamble Company | Process for making films from nonwoven webs |
EP3533908A1 (en) | 2010-07-02 | 2019-09-04 | The Procter & Gamble Company | Nonwoven web comprising one or more active agents |
WO2012009660A2 (en) | 2010-07-15 | 2012-01-19 | The Procter & Gamble Company | Detergent compositions comprising microbially produced fatty alcohols and derivatives thereof |
WO2012009525A2 (en) | 2010-07-15 | 2012-01-19 | The Procter & Gamble Company | Compositions comprising a near terminal-branched compound and methods of making the same |
WO2012112828A1 (en) | 2011-02-17 | 2012-08-23 | The Procter & Gamble Company | Bio-based linear alkylphenyl sulfonates |
WO2012138423A1 (en) | 2011-02-17 | 2012-10-11 | The Procter & Gamble Company | Compositions comprising mixtures of c10-c13 alkylphenyl sulfonates |
US9193937B2 (en) | 2011-02-17 | 2015-11-24 | The Procter & Gamble Company | Mixtures of C10-C13 alkylphenyl sulfonates |
WO2013002786A1 (en) | 2011-06-29 | 2013-01-03 | Solae | Baked food compositions comprising soy whey proteins that have been isolated from processing streams |
WO2013043805A1 (en) | 2011-09-20 | 2013-03-28 | The Procter & Gamble Company | Detergent compositions comprising primary surfactant systems comprising highly branched surfactants especially isoprenoid - based surfactants |
WO2013043857A1 (en) | 2011-09-20 | 2013-03-28 | The Procter & Gamble Company | Detergent compositions comprising sustainable surfactant systems comprising isoprenoid-derived surfactants |
WO2013043803A2 (en) | 2011-09-20 | 2013-03-28 | The Procter & Gamble Company | Detergent compositions comprising specific blend ratios of isoprenoid-based surfactants |
WO2013043855A2 (en) | 2011-09-20 | 2013-03-28 | The Procter & Gamble Company | High suds detergent compositions comprising isoprenoid-based surfactants |
WO2013043852A2 (en) | 2011-09-20 | 2013-03-28 | The Procter & Gamble Company | Easy-rinse detergent compositions comprising isoprenoid-based surfactants |
WO2013070559A1 (en) | 2011-11-11 | 2013-05-16 | The Procter & Gamble Company | Surface treatment compositions including shielding salts |
WO2013070560A1 (en) | 2011-11-11 | 2013-05-16 | The Procter & Gamble Company | Surface treatment compositions including shielding salts |
FR2985273A1 (en) | 2012-01-04 | 2013-07-05 | Procter & Gamble | FIBROUS STRUCTURES CONTAINING ASSETS AND HAVING MULTIPLE REGIONS |
EP3719192A1 (en) | 2012-01-04 | 2020-10-07 | The Procter & Gamble Company | Fibrous structures comprising particles and methods for making same |
EP3369845A1 (en) | 2012-01-04 | 2018-09-05 | The Procter & Gamble Company | Active containing fibrous structures with multiple regions having differing densities |
US11970821B2 (en) | 2013-12-09 | 2024-04-30 | The Procter & Gamble Company | Fibrous structures including an active agent and having a graphic printed thereon |
FR3014456A1 (en) | 2013-12-09 | 2015-06-12 | Procter & Gamble | |
WO2015088826A1 (en) | 2013-12-09 | 2015-06-18 | The Procter & Gamble Company | Fibrous structures including an active agent and having a graphic printed thereon |
US11795622B2 (en) | 2013-12-09 | 2023-10-24 | The Procter & Gamble Company | Fibrous structures including an active agent and having a graphic printed thereon |
EP4253649A2 (en) | 2013-12-09 | 2023-10-04 | The Procter & Gamble Company | Fibrous structures including an active agent and having a graphic printed thereon |
US11624156B2 (en) | 2013-12-09 | 2023-04-11 | The Procter & Gamble Company | Fibrous structures including an active agent and having a graphic printed thereon |
US10494767B2 (en) | 2013-12-09 | 2019-12-03 | The Procter & Gamble Company | Fibrous structures including an active agent and having a graphic printed thereon |
EP3572572A1 (en) | 2013-12-09 | 2019-11-27 | The Procter & Gamble Company | Fibrous structures including an active agent and having a graphic printed thereon |
DE112014005598B4 (en) | 2013-12-09 | 2022-06-09 | The Procter & Gamble Company | Fibrous structures including an active substance and with graphics printed on it |
EP3805350A1 (en) | 2013-12-09 | 2021-04-14 | The Procter & Gamble Company | Fibrous structures including an active agent and having a graphic printed thereon |
US11293144B2 (en) | 2013-12-09 | 2022-04-05 | The Procter & Gamble Company | Fibrous structures including an active agent and having a graphic printed thereon |
WO2015112671A1 (en) | 2014-01-24 | 2015-07-30 | The Procter & Gamble Company | Consumer product compositions |
CN105059764A (en) * | 2015-07-09 | 2015-11-18 | 滁州市润达溶剂有限公司 | Heptanes liquefaction outflow device |
CN105059764B (en) * | 2015-07-09 | 2017-12-22 | 滁州市润达溶剂有限公司 | Liquefaction bleeder for heptane |
EP3991962A1 (en) | 2017-01-27 | 2022-05-04 | The Procter & Gamble Company | Active agent-containing articles that exhibit consumer acceptable article in-use properties |
DE112018000558T5 (en) | 2017-01-27 | 2019-10-10 | The Procter & Gamble Company | Active substance-containing articles which have acceptable consumer properties acceptable to the consumer |
WO2018140431A1 (en) | 2017-01-27 | 2018-08-02 | The Procter & Gamble Company | Active agent-containing articles that exhibit consumer acceptable article in-use properties |
DE112018000563T5 (en) | 2017-01-27 | 2019-10-24 | The Procter & Gamble Company | Active substance-containing articles which have acceptable consumer properties acceptable to the consumer |
WO2018140432A1 (en) | 2017-01-27 | 2018-08-02 | The Procter & Gamble Company | Active agent-containing articles that exhibit consumer acceptable article in-use properties |
EP3881900A1 (en) | 2017-01-27 | 2021-09-22 | The Procter & Gamble Company | Active agent-containing articles that exhibit consumer acceptable article in-use properties |
EP3915643A1 (en) | 2017-01-27 | 2021-12-01 | The Procter & Gamble Company | Active agent-containing articles that exhibit consumer acceptable article in-use properties |
DE112018000565T5 (en) | 2017-01-27 | 2019-10-24 | The Procter & Gamble Company | Active substance-containing articles which have acceptable consumer properties acceptable to the consumer |
DE112018000568T5 (en) | 2017-01-27 | 2019-10-17 | The Procter & Gamble Company | Active substance-containing articles and product shipping arrangements for enclosing the same |
WO2018140472A1 (en) | 2017-01-27 | 2018-08-02 | The Procter & Gamble Company | Active agent-containing articles that exhibit consumer acceptable article in-use properties |
EP4197598A1 (en) | 2017-01-27 | 2023-06-21 | The Procter & Gamble Company | Active agent-containing articles that exhibit consumer acceptable article in-use properties |
WO2018140454A1 (en) | 2017-01-27 | 2018-08-02 | The Procter & Gamble Company | Active agent-containing articles and product-shipping assemblies for containing the same |
WO2020123889A1 (en) | 2018-12-14 | 2020-06-18 | The Procter & Gamble Company | Foaming fibrous structures comprising particles and methods for making same |
WO2021026556A1 (en) | 2019-08-02 | 2021-02-11 | The Procter & Gamble Company | Foaming compositions for producing a stable foam and methods for making same |
WO2021097004A1 (en) | 2019-11-15 | 2021-05-20 | The Procter & Gamble Company | Graphic-containing soluble articles and methods for making same |
WO2022251838A1 (en) | 2021-05-28 | 2022-12-01 | The Procter & Gamble Company | Natural polymer-based fibrous elements comprising a surfactant and methods for making same |
WO2023057367A1 (en) | 2021-10-08 | 2023-04-13 | Unilever Ip Holdings B.V. | Laundry composition |
Similar Documents
Publication | Publication Date | Title |
---|---|---|
US3600319A (en) | Process for application of enzymes to spray-dried detergent granules | |
US3451935A (en) | Granular enzyme-containing laundry composition | |
US3519570A (en) | Enzyme - containing detergent compositions and a process for conglutination of enzymes and detergent compositions | |
US5855625A (en) | Detergent compositions | |
US3798181A (en) | Enzymatic detergent bar | |
US5551990A (en) | Enzymatic dishwashing and rinsing composition | |
EP0766726B1 (en) | Dishwashing compositions | |
US6656898B1 (en) | Enzyme composite particles having an acidic barrier and a physical barrier coating | |
GB2213153A (en) | A stabilized enzyme system for use in aqueous liquid built detergent compositions | |
US3650967A (en) | Enzymatic granules | |
US5156761A (en) | Method of stabilizing an enzymatic liquid detergent composition | |
US3600318A (en) | Enzyme-containing detergent compositions for neutral washing | |
US5501820A (en) | Aqueous enzymatic detergent compositions | |
AU629116B2 (en) | Process for preparing liquid enzymatic detergent compositions | |
CA2096256C (en) | Liquid detergent composition containing lipase and protease | |
US5071586A (en) | Protease-containing compositions stabilized by propionic acid or salt thereof | |
US3781228A (en) | Laundry product containing enzyme | |
US3655568A (en) | Enzyme containing detergent composition having improved physical and stability characteristics | |
US3519379A (en) | Soaking and laundering process | |
AU772325B2 (en) | Laundry detergent composition containing high level of protease enzyme | |
AU642276B2 (en) | Protease-containing liquid detergent compositions | |
US3634267A (en) | Enzyme additives | |
GB1573406A (en) | Bleaching detergent compositions | |
US6235697B1 (en) | Laundry detergent composition containing level protease enzyme | |
JPH0267399A (en) | Bleaching detergent composition |