CA2002440A1 - Enzyme-containing detergent compositions - Google Patents
Enzyme-containing detergent compositionsInfo
- Publication number
- CA2002440A1 CA2002440A1 CA 2002440 CA2002440A CA2002440A1 CA 2002440 A1 CA2002440 A1 CA 2002440A1 CA 2002440 CA2002440 CA 2002440 CA 2002440 A CA2002440 A CA 2002440A CA 2002440 A1 CA2002440 A1 CA 2002440A1
- Authority
- CA
- Canada
- Prior art keywords
- weight
- detergent
- composition
- active material
- builder
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Abandoned
Links
- 239000000203 mixture Substances 0.000 title claims abstract description 62
- 239000003599 detergent Substances 0.000 title claims abstract description 39
- 102000004190 Enzymes Human genes 0.000 title claims abstract description 21
- 108090000790 Enzymes Proteins 0.000 title claims abstract description 21
- 230000002366 lipolytic effect Effects 0.000 claims abstract description 19
- 239000000344 soap Substances 0.000 claims abstract description 16
- 229910000503 Na-aluminosilicate Inorganic materials 0.000 claims abstract description 15
- 235000012217 sodium aluminium silicate Nutrition 0.000 claims abstract description 15
- 239000011149 active material Substances 0.000 claims abstract description 14
- 239000000429 sodium aluminium silicate Substances 0.000 claims abstract description 14
- URGAHOPLAPQHLN-UHFFFAOYSA-N sodium aluminosilicate Chemical compound [Na+].[Al+3].[O-][Si]([O-])=O.[O-][Si]([O-])=O URGAHOPLAPQHLN-UHFFFAOYSA-N 0.000 claims abstract description 14
- 125000000129 anionic group Chemical group 0.000 claims abstract description 7
- 239000004615 ingredient Substances 0.000 claims abstract description 6
- BVKZGUZCCUSVTD-UHFFFAOYSA-L Carbonate Chemical compound [O-]C([O-])=O BVKZGUZCCUSVTD-UHFFFAOYSA-L 0.000 claims abstract description 3
- KRKNYBCHXYNGOX-UHFFFAOYSA-K Citrate Chemical compound [O-]C(=O)CC(O)(CC([O-])=O)C([O-])=O KRKNYBCHXYNGOX-UHFFFAOYSA-K 0.000 claims abstract description 3
- BPQQTUXANYXVAA-UHFFFAOYSA-N Orthosilicate Chemical compound [O-][Si]([O-])([O-])[O-] BPQQTUXANYXVAA-UHFFFAOYSA-N 0.000 claims abstract description 3
- 239000001509 sodium citrate Substances 0.000 claims abstract 2
- 238000005469 granulation Methods 0.000 claims description 34
- 230000003179 granulation Effects 0.000 claims description 34
- 239000011230 binding agent Substances 0.000 claims description 8
- 239000003795 chemical substances by application Substances 0.000 claims description 6
- 238000000280 densification Methods 0.000 claims description 5
- 238000002360 preparation method Methods 0.000 claims description 5
- 239000007788 liquid Substances 0.000 claims description 4
- 239000007858 starting material Substances 0.000 claims description 3
- 108090001060 Lipase Proteins 0.000 description 34
- 102000004882 Lipase Human genes 0.000 description 34
- 239000004367 Lipase Substances 0.000 description 31
- 235000019421 lipase Nutrition 0.000 description 31
- 239000000843 powder Substances 0.000 description 26
- 238000000034 method Methods 0.000 description 18
- HNPSIPDUKPIQMN-UHFFFAOYSA-N dioxosilane;oxo(oxoalumanyloxy)alumane Chemical compound O=[Si]=O.O=[Al]O[Al]=O HNPSIPDUKPIQMN-UHFFFAOYSA-N 0.000 description 15
- 239000008187 granular material Substances 0.000 description 12
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 12
- 239000010457 zeolite Substances 0.000 description 12
- 238000009472 formulation Methods 0.000 description 11
- 229910021536 Zeolite Inorganic materials 0.000 description 10
- 238000010298 pulverizing process Methods 0.000 description 10
- 239000004094 surface-active agent Substances 0.000 description 9
- 229910000323 aluminium silicate Inorganic materials 0.000 description 8
- 239000002245 particle Substances 0.000 description 8
- 239000004744 fabric Substances 0.000 description 7
- 239000000463 material Substances 0.000 description 7
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 description 6
- CDBYLPFSWZWCQE-UHFFFAOYSA-L Sodium Carbonate Chemical compound [Na+].[Na+].[O-]C([O-])=O CDBYLPFSWZWCQE-UHFFFAOYSA-L 0.000 description 6
- 235000021588 free fatty acids Nutrition 0.000 description 6
- 238000001694 spray drying Methods 0.000 description 6
- 229910000632 Alusil Inorganic materials 0.000 description 5
- -1 primary alcohol sulphates Chemical class 0.000 description 5
- 238000005406 washing Methods 0.000 description 5
- 229920000742 Cotton Polymers 0.000 description 4
- 239000004115 Sodium Silicate Substances 0.000 description 4
- PMZURENOXWZQFD-UHFFFAOYSA-L Sodium Sulfate Chemical compound [Na+].[Na+].[O-]S([O-])(=O)=O PMZURENOXWZQFD-UHFFFAOYSA-L 0.000 description 4
- 239000003945 anionic surfactant Substances 0.000 description 4
- 230000000052 comparative effect Effects 0.000 description 4
- 230000000694 effects Effects 0.000 description 4
- 239000002736 nonionic surfactant Substances 0.000 description 4
- 229920000728 polyester Polymers 0.000 description 4
- NTHWMYGWWRZVTN-UHFFFAOYSA-N sodium silicate Chemical compound [Na+].[Na+].[O-][Si]([O-])=O NTHWMYGWWRZVTN-UHFFFAOYSA-N 0.000 description 4
- 229910052911 sodium silicate Inorganic materials 0.000 description 4
- 239000000654 additive Substances 0.000 description 3
- 238000004140 cleaning Methods 0.000 description 3
- 239000000047 product Substances 0.000 description 3
- 229910000029 sodium carbonate Inorganic materials 0.000 description 3
- 229910019142 PO4 Inorganic materials 0.000 description 2
- 108091005804 Peptidases Proteins 0.000 description 2
- 239000004365 Protease Substances 0.000 description 2
- 102100037486 Reverse transcriptase/ribonuclease H Human genes 0.000 description 2
- 102000005158 Subtilisins Human genes 0.000 description 2
- 108010056079 Subtilisins Proteins 0.000 description 2
- BAECOWNUKCLBPZ-HIUWNOOHSA-N Triolein Natural products O([C@H](OCC(=O)CCCCCCC/C=C\CCCCCCCC)COC(=O)CCCCCCC/C=C\CCCCCCCC)C(=O)CCCCCCC/C=C\CCCCCCCC BAECOWNUKCLBPZ-HIUWNOOHSA-N 0.000 description 2
- PHYFQTYBJUILEZ-UHFFFAOYSA-N Trioleoylglycerol Natural products CCCCCCCCC=CCCCCCCCC(=O)OCC(OC(=O)CCCCCCCC=CCCCCCCCC)COC(=O)CCCCCCCC=CCCCCCCCC PHYFQTYBJUILEZ-UHFFFAOYSA-N 0.000 description 2
- 235000010724 Wisteria floribunda Nutrition 0.000 description 2
- 230000009286 beneficial effect Effects 0.000 description 2
- 229920001577 copolymer Polymers 0.000 description 2
- 230000009260 cross reactivity Effects 0.000 description 2
- 238000007580 dry-mixing Methods 0.000 description 2
- 230000001900 immune effect Effects 0.000 description 2
- 244000005700 microbiome Species 0.000 description 2
- 235000014366 other mixer Nutrition 0.000 description 2
- 239000011236 particulate material Substances 0.000 description 2
- 239000002304 perfume Substances 0.000 description 2
- 239000010452 phosphate Substances 0.000 description 2
- NBIIXXVUZAFLBC-UHFFFAOYSA-K phosphate Chemical compound [O-]P([O-])([O-])=O NBIIXXVUZAFLBC-UHFFFAOYSA-K 0.000 description 2
- 239000000377 silicon dioxide Substances 0.000 description 2
- 238000002791 soaking Methods 0.000 description 2
- 239000011734 sodium Substances 0.000 description 2
- 229910052938 sodium sulfate Inorganic materials 0.000 description 2
- 235000011152 sodium sulphate Nutrition 0.000 description 2
- PHYFQTYBJUILEZ-IUPFWZBJSA-N triolein Chemical compound CCCCCCCC\C=C/CCCCCCCC(=O)OCC(OC(=O)CCCCCCC\C=C/CCCCCCCC)COC(=O)CCCCCCC\C=C/CCCCCCCC PHYFQTYBJUILEZ-IUPFWZBJSA-N 0.000 description 2
- 229940117972 triolein Drugs 0.000 description 2
- 241000588986 Alcaligenes Species 0.000 description 1
- 241000589513 Burkholderia cepacia Species 0.000 description 1
- OYPRJOBELJOOCE-UHFFFAOYSA-N Calcium Chemical compound [Ca] OYPRJOBELJOOCE-UHFFFAOYSA-N 0.000 description 1
- BHPQYMZQTOCNFJ-UHFFFAOYSA-N Calcium cation Chemical group [Ca+2] BHPQYMZQTOCNFJ-UHFFFAOYSA-N 0.000 description 1
- 108090000371 Esterases Proteins 0.000 description 1
- 241000223198 Humicola Species 0.000 description 1
- 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 1
- FYYHWMGAXLPEAU-UHFFFAOYSA-N Magnesium Chemical compound [Mg] FYYHWMGAXLPEAU-UHFFFAOYSA-N 0.000 description 1
- 241000589516 Pseudomonas Species 0.000 description 1
- 241000223257 Thermomyces Species 0.000 description 1
- 241000223258 Thermomyces lanuginosus Species 0.000 description 1
- 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 1
- 239000012190 activator Substances 0.000 description 1
- ANBBXQWFNXMHLD-UHFFFAOYSA-N aluminum;sodium;oxygen(2-) Chemical compound [O-2].[O-2].[Na+].[Al+3] ANBBXQWFNXMHLD-UHFFFAOYSA-N 0.000 description 1
- 239000007844 bleaching agent Substances 0.000 description 1
- 239000011575 calcium Substances 0.000 description 1
- 229910052791 calcium Inorganic materials 0.000 description 1
- 229910001424 calcium ion Inorganic materials 0.000 description 1
- 239000000378 calcium silicate Substances 0.000 description 1
- 229910052918 calcium silicate Inorganic materials 0.000 description 1
- OYACROKNLOSFPA-UHFFFAOYSA-N calcium;dioxido(oxo)silane Chemical compound [Ca+2].[O-][Si]([O-])=O OYACROKNLOSFPA-UHFFFAOYSA-N 0.000 description 1
- 239000001768 carboxy methyl cellulose Substances 0.000 description 1
- 239000012876 carrier material Substances 0.000 description 1
- 238000006243 chemical reaction Methods 0.000 description 1
- 229910052681 coesite Inorganic materials 0.000 description 1
- 229910052906 cristobalite Inorganic materials 0.000 description 1
- 238000005520 cutting process Methods 0.000 description 1
- 230000001419 dependent effect Effects 0.000 description 1
- 230000006866 deterioration Effects 0.000 description 1
- 235000014113 dietary fatty acids Nutrition 0.000 description 1
- 239000000194 fatty acid Substances 0.000 description 1
- 229930195729 fatty acid Natural products 0.000 description 1
- 239000012467 final product Substances 0.000 description 1
- 239000010419 fine particle Substances 0.000 description 1
- 239000006260 foam Substances 0.000 description 1
- 230000036571 hydration Effects 0.000 description 1
- 238000006703 hydration reaction Methods 0.000 description 1
- 238000005342 ion exchange Methods 0.000 description 1
- 235000019626 lipase activity Nutrition 0.000 description 1
- 239000011777 magnesium Substances 0.000 description 1
- 229910052749 magnesium Inorganic materials 0.000 description 1
- 238000004519 manufacturing process Methods 0.000 description 1
- 239000011159 matrix material Substances 0.000 description 1
- 238000012986 modification Methods 0.000 description 1
- 230000004048 modification Effects 0.000 description 1
- JRZJOMJEPLMPRA-UHFFFAOYSA-N olefin Natural products CCCCCCCC=C JRZJOMJEPLMPRA-UHFFFAOYSA-N 0.000 description 1
- 230000000704 physical effect Effects 0.000 description 1
- 229920000642 polymer Polymers 0.000 description 1
- 235000012239 silicon dioxide Nutrition 0.000 description 1
- 239000002002 slurry Substances 0.000 description 1
- 229910052708 sodium Inorganic materials 0.000 description 1
- 229910001388 sodium aluminate Inorganic materials 0.000 description 1
- 235000019812 sodium carboxymethyl cellulose Nutrition 0.000 description 1
- 229920001027 sodium carboxymethylcellulose Polymers 0.000 description 1
- 229940074404 sodium succinate Drugs 0.000 description 1
- ZDQYSKICYIVCPN-UHFFFAOYSA-L sodium succinate (anhydrous) Chemical compound [Na+].[Na+].[O-]C(=O)CCC([O-])=O ZDQYSKICYIVCPN-UHFFFAOYSA-L 0.000 description 1
- 239000012798 spherical particle Substances 0.000 description 1
- 238000003756 stirring Methods 0.000 description 1
- 229910052682 stishovite Inorganic materials 0.000 description 1
- 239000000126 substance Substances 0.000 description 1
- 125000001273 sulfonato group Chemical group [O-]S(*)(=O)=O 0.000 description 1
- 239000003760 tallow Substances 0.000 description 1
- 238000004448 titration Methods 0.000 description 1
- 229910052905 tridymite Inorganic materials 0.000 description 1
- 239000004711 α-olefin Substances 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C11—ANIMAL OR VEGETABLE OILS, FATS, FATTY SUBSTANCES OR WAXES; FATTY ACIDS THEREFROM; DETERGENTS; CANDLES
- C11D—DETERGENT COMPOSITIONS; USE OF SINGLE SUBSTANCES AS DETERGENTS; SOAP OR SOAP-MAKING; RESIN SOAPS; RECOVERY OF GLYCEROL
- C11D3/00—Other compounding ingredients of detergent compositions covered in group C11D1/00
- C11D3/02—Inorganic compounds ; Elemental compounds
- C11D3/12—Water-insoluble compounds
- C11D3/124—Silicon containing, e.g. silica, silex, quartz or glass beads
- C11D3/1246—Silicates, e.g. diatomaceous earth
- C11D3/1253—Layer silicates, e.g. talcum, kaolin, clay, bentonite, smectite, montmorillonite, hectorite or attapulgite
- C11D3/126—Layer silicates, e.g. talcum, kaolin, clay, bentonite, smectite, montmorillonite, hectorite or attapulgite in solid compositions
-
- C—CHEMISTRY; METALLURGY
- C11—ANIMAL OR VEGETABLE OILS, FATS, FATTY SUBSTANCES OR WAXES; FATTY ACIDS THEREFROM; DETERGENTS; CANDLES
- C11D—DETERGENT COMPOSITIONS; USE OF SINGLE SUBSTANCES AS DETERGENTS; SOAP OR SOAP-MAKING; RESIN SOAPS; RECOVERY OF GLYCEROL
- C11D3/00—Other compounding ingredients of detergent compositions covered in group C11D1/00
- C11D3/02—Inorganic compounds ; Elemental compounds
- C11D3/12—Water-insoluble compounds
- C11D3/124—Silicon containing, e.g. silica, silex, quartz or glass beads
- C11D3/1246—Silicates, e.g. diatomaceous earth
- C11D3/128—Aluminium silicates, e.g. zeolites
-
- 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
- C11D3/38627—Preparations containing enzymes, e.g. protease or amylase containing lipase
Landscapes
- Chemical & Material Sciences (AREA)
- Life Sciences & Earth Sciences (AREA)
- Engineering & Computer Science (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Oil, Petroleum & Natural Gas (AREA)
- Wood Science & Technology (AREA)
- Organic Chemistry (AREA)
- Inorganic Chemistry (AREA)
- Detergent Compositions (AREA)
Abstract
ABSTRACT
A granular detergent composition or component therefor, which comprises:
(a) from 6% to 35%, often over 17%, by weight of non-soap detergent-active material consisting at least partially of anionic and/or nonionic detergent-active material;
(b) at least 45% by weight of builder (b1) the builder including at least 28%, e.g. up to 45%, by weight (anhydrous basis) of crystalline or amorphous sodium aluminosilicate and/or citrate, carbonate, or layered silicate builder, (c) a lipolytic enzyme the weight ratio of (b1) to (a) being from 0.9:1 to 2.6:1, preferably from 1.2:1 to 1.8:1; and other detergent ingredients to 100% by weight.
A granular detergent composition or component therefor, which comprises:
(a) from 6% to 35%, often over 17%, by weight of non-soap detergent-active material consisting at least partially of anionic and/or nonionic detergent-active material;
(b) at least 45% by weight of builder (b1) the builder including at least 28%, e.g. up to 45%, by weight (anhydrous basis) of crystalline or amorphous sodium aluminosilicate and/or citrate, carbonate, or layered silicate builder, (c) a lipolytic enzyme the weight ratio of (b1) to (a) being from 0.9:1 to 2.6:1, preferably from 1.2:1 to 1.8:1; and other detergent ingredients to 100% by weight.
Description
- 1 - C.3285 ENZYME-CONTAINING DETERGENT COMPOSITIONS
This invention relates to detergent compositions, and in particular those containing lipolytic enzyme.
Detergent compositions comprising lipase are known. For example GB 1 372 034 (Unilever~ discloses lipase from Pseudomonas in specific nonionic-containing ldetergent~
compositions for soaking fabrics.
USP 3 950 277 (Procter & Gamble) also describes fabric-soaking compositions: the described compositions comprise lipase and lipase activators and a number of lipases from microorganism and other sources are mentioned: those particularly mentioned as preferred are Amano CE, Amano M-AP, Takeda 1969-4-9, and Meito MY-30 lipases, but no indications are given of the form in which the lipase is to be prepared or used.
USP 4 011 169/NL 74 08763 (Procter & Gamble) describes the use of a similar range of enzymes in the preparation of ; additives for washing agents (detergent compositions).
, ... , ,, . . . . -- 2 - C.3285 EP 0 214 761 (Novo) and EP 0 258 068 (Novo), each give detailed description of lipases from certain microorganisms, and also give certain uses in detergent additives and detergent compositions for the enzymes described. EP 0 214 761 gives detailed description of lipases derived from organisms of the species Pseudomonas cepacia, an`d certain uses therefor. EP 0 258 068 gives detailed description of lipases derived from organisms of the genus Thermomyces/Humicola, and certain uses therefor.
Also believed to be in use in certain areas is a lipase-containing granular detergent composition containing about 37% detergent actives including 5~ nonionic detergent and the remainder substantially anionic detergent, about 16%
zeolite, about 70-90 LU/g lipase, plus protease and other normal detergent additives.
An aim of this invention is the provision of a lipase-containing granular detergent composition with a particularly effective formulation for supporting the action of lipase enzyme.
According to the present invention, there is provided a granular detergent composition or component therefor, which comprises-(a) from 6% to 35%, often over 17%, by weightof non-soap detergent-active material consisting at least partially of anionic and/or nonionic detergent-active material;
~b) at least 45~ by weight of builder, ~` " ' .
::
` ` Z002440 ` ``- `````~````` ~ `
This invention relates to detergent compositions, and in particular those containing lipolytic enzyme.
Detergent compositions comprising lipase are known. For example GB 1 372 034 (Unilever~ discloses lipase from Pseudomonas in specific nonionic-containing ldetergent~
compositions for soaking fabrics.
USP 3 950 277 (Procter & Gamble) also describes fabric-soaking compositions: the described compositions comprise lipase and lipase activators and a number of lipases from microorganism and other sources are mentioned: those particularly mentioned as preferred are Amano CE, Amano M-AP, Takeda 1969-4-9, and Meito MY-30 lipases, but no indications are given of the form in which the lipase is to be prepared or used.
USP 4 011 169/NL 74 08763 (Procter & Gamble) describes the use of a similar range of enzymes in the preparation of ; additives for washing agents (detergent compositions).
, ... , ,, . . . . -- 2 - C.3285 EP 0 214 761 (Novo) and EP 0 258 068 (Novo), each give detailed description of lipases from certain microorganisms, and also give certain uses in detergent additives and detergent compositions for the enzymes described. EP 0 214 761 gives detailed description of lipases derived from organisms of the species Pseudomonas cepacia, an`d certain uses therefor. EP 0 258 068 gives detailed description of lipases derived from organisms of the genus Thermomyces/Humicola, and certain uses therefor.
Also believed to be in use in certain areas is a lipase-containing granular detergent composition containing about 37% detergent actives including 5~ nonionic detergent and the remainder substantially anionic detergent, about 16%
zeolite, about 70-90 LU/g lipase, plus protease and other normal detergent additives.
An aim of this invention is the provision of a lipase-containing granular detergent composition with a particularly effective formulation for supporting the action of lipase enzyme.
According to the present invention, there is provided a granular detergent composition or component therefor, which comprises-(a) from 6% to 35%, often over 17%, by weightof non-soap detergent-active material consisting at least partially of anionic and/or nonionic detergent-active material;
~b) at least 45~ by weight of builder, ~` " ' .
::
` ` Z002440 ` ``- `````~````` ~ `
- 3 - C.3285 (bl) the builder including at least 28~, e.g.
up to 45~, by weight ~anhydrous basis) of crystalline or amorphous sodium aluminosilicate S and/or citrate, carbonate, or layered silicate builder, (c) a lipolytic enzyme, the weight ratio of (bl) to (a) being from 0.9:1 to 2.6:1, preferably from 1.2:1 to 1.8:1; and other detergent ingredients to 100% by weight.
According to the invention, certain of the compositions and components (adjuncts) therefor, including preferred compositions, can be prepared by treating a particulate starting material comprising:
(a) from 5 to 3S% by weight of non-soap detergent-active material consisting at least partially of anionic detergent-active material, and (b) from 28 to 45~ by weight (anhydrous basis) of crystalline or amorphous sodium aluminosilicate, the weight ratio of (b) to (a) being at least 0.9:1, and other detergent components to 100~ by weight, in a high-speed mixer in the presence of a liquid binder but in the absence of a finely divided particulate agent for improving surface properties, whereby granulation and densification to a bulk density of at least 650 g/litre are effected, and adding a lipolytic enzyme preparation after the granulation stage which has been carried out in the high-speed mixer.
Certain embodiments of the invention have a high bulk density, e.g. a bulk density of at least 650 g/litre.
' ' `~ '` ;, ,''' - ~ ' ':
, .
up to 45~, by weight ~anhydrous basis) of crystalline or amorphous sodium aluminosilicate S and/or citrate, carbonate, or layered silicate builder, (c) a lipolytic enzyme, the weight ratio of (bl) to (a) being from 0.9:1 to 2.6:1, preferably from 1.2:1 to 1.8:1; and other detergent ingredients to 100% by weight.
According to the invention, certain of the compositions and components (adjuncts) therefor, including preferred compositions, can be prepared by treating a particulate starting material comprising:
(a) from 5 to 3S% by weight of non-soap detergent-active material consisting at least partially of anionic detergent-active material, and (b) from 28 to 45~ by weight (anhydrous basis) of crystalline or amorphous sodium aluminosilicate, the weight ratio of (b) to (a) being at least 0.9:1, and other detergent components to 100~ by weight, in a high-speed mixer in the presence of a liquid binder but in the absence of a finely divided particulate agent for improving surface properties, whereby granulation and densification to a bulk density of at least 650 g/litre are effected, and adding a lipolytic enzyme preparation after the granulation stage which has been carried out in the high-speed mixer.
Certain embodiments of the invention have a high bulk density, e.g. a bulk density of at least 650 g/litre.
' ' `~ '` ;, ,''' - ~ ' ':
, .
- 4 - C.3285 It is useful and surprising that lipase activity is particularly well supported in the presence of the quantities of builder set out herein.
~he lipolytic enzyme can usefully be added in the form of a granular composition of lipolytic enzyme with carrier material.
The added amount of lipolytic enzyme can be chosen within wide limits, for example 30 to 30,000 LU/g of granular detergent composition, e.g. at least 300 LU/g, often usefully at least 500 LU/g, sometimes preferably above 1000 LU/g or above 3000 LU/g or more.
Ihe lipolytic enzyme can be chosen from among a wide range of lipases: in particular the lipases described in for example the following patent specifications, EP 0214761 (Novo), EP 0258068 (Novo) and especially lipases showing immunological cross-reactivity with antisera raised against lipase from Thermomyces lanuginosus ATCC 22070, EP 0205208 (Unilever) and EP 0206390 (Unilever), and especially lipases showing immunological cross-reactivity with antisera raised against lipase with Chromobacter viscosum var lipolyticum NRRL B-3673, or against lipase from Alcaligenes PL-679, ATCC 31371 and FERM-P 3783, also the lipases described in specifications WO 87/00859 (Gist-Brocades) and EP 0204284 (Sapporo Breweries). Suitable in particular are for example the following commercially available lipase preparations: Novo Lipolase, Amano lipases CE, P, B, AP, M-AP, AML, and CES, and Meito lipases MY-30, OF, and PL, also esterase MM, Lipozym, SP225, SP285, Saiken lipase, Enzeco lipase, Toyo Jozo lipase and Diosynth lipase (Trade Marks).
... .
~002440 ~ 5 - C.3285 It has now been surprisingly found that lipolytic enzyme e~erts a comparatively greater effect when used in compositions of the type described above, than when used in comparative compositions as illustrated in the lipolytic example below.
According to preferred embodiments, the invention provides detergent powders combining high bulk density, good powder properties and excellent washing and cleaning performance, that can be prepared easily and conveniently.
These detergent compositions owe their combination of excellent properties and ready processability to a moderate content of surfactant, at least part of which is anionic, and a relatively high level of sodium aluminosilicate builder. It has been found that when the absolute amounts of aluminosilicate builder and surfactant, and the ratio of one to the other, are suitably chosen, the spray-dried base powder may be pulverised and granulated in a high-speed mixer without the need for the use of an "agent for improving surface properties" during the granulation step as prescribed by JP 61 069897A (Kao). The resulting dense granulate has good flow properties and is at least equal in washing and cleaning performance and cold water dispersability to the compositions described in the Kao specification which contain substantially higher levels of surfactant.
The aluminosilicate builder present in the compositions may be crystalline or amorphous or a mixture thereof, and can have the general formula 0.8-1.5 Na20 . A1203 . 0.8-6 SiO2.
- 6 - C.3285 These materials contain some bound water and should in most cases have a calcium ion exchange capacity of at least about 50 mg CaO/g. The preferred aluminosilicates contain 1.5-3.5 SiO2 units (in the formula above) and have a particle size of not more than about 100 microns, preferably not more than about 20 microns. Both amorphous and crystalline aluminosilicates can be made readily by reaction between sodium silicate and sodium aluminate, as amply described in the literatur~.
Crystalline aluminosilicates ~zeolites) are preferred for use in the present invention. Suitable materials are described, for example, in GB 1 473 201 (Henkel) and GB 1 429 143 (Procter & Gamble). The preferred sodium aluminosilicates of this type are the well-known commercially available zeolites A and X, and mixtures thereof. Especially preferred for use in the present invention is Type 4A zeolite.
The ratio of aluminosilicate builder (anhydrous basis) to total non-soap surfactant in the compositions is preferably within the range of from 1.2:1 to 1.3:1.
The non-soap surfactant present consists at least partially of anionic surfactant. Suitable anionic surfactants are well known to those skilled in the art, and include linear alkylbenzene sulphonates, primary alcohol sulphates, alkyl ether sulphates, alpha-olefin sulphonates, internal olefin sulphonates, fatty acid ester sulphonates and combinations thereof.
If desired, nonionic surfactant may also be present, preferably in a minor amount. Suitably the surfactant . . .
- 7 - C.3~85 c:omponent of the compositions of the invention may be - c:onstituted by 10 to 35~ by weight of anionic surfactant and 0 to 10~ by weight of nonionic surfactant.
If desired, soap may also be present, to provide foam control and additional detergency and builder power; soap is not included in the 17 to 35% figure given above for the total surfactant content of the compositions.
The compositions preferably do not contain more than 5~ by weight of phosphate builders, and are more preferably substantially free of phosphate builders.
The particulate starting composition may be prepared by any suitable tower or non-tower method, for example, spray-drying or dry-mixing; spray-drying is preferred.
The final granulate may be used as a complete detergent composition in its own right. Alternatively, additional ingredients such as enzymes, bleach and perfume that are not suitable for undergoing the granulation process and the steps that precede it may be admixed to the granulate to make a final product.
In preferred cases the final granulate has a bulk density of at least 650 g/litre and more preferably at least 700 g/litre. It is preferably also characterised by an especially low particle porosity, not exceeding 25~ and preferably not exceeding 20%, which distinguishes it from even the densest powders prepared by spray-drying alone.
In suitable examples of processes for making the preferred high-bulk-density compositions, a particulate starting material (detergent base powder) prepared by any suitable method is treated in a high-speed mixer to increase its :, ;. . .
- 8 - C.3285 bulk density and simultaneously to improve its powder - properties. The process is especially useful for the densification of a spray-dried powder, and provides a route for the production of very dense granular detergent compositions, having excellent cleaning performance, containing low to moderate levels of anionic surfactant and high levels of aluminosilicate builder.
A preferred starting powder comprises:
(a) from 17 to 35~ by weight of non-soap detergent-active material consisting at least partially of anionic detergent-active material, and (b) from 28 to 45% by weight of crystalline or amorphous sodium aluminosilicate, the weight ratio of (b) to (a) being from 0.9:1 to 2.6:1, and other detergent components to 100~ by weight.
On treatment in a high-speed mixer by an example of the process set out above, this can gives a granular detergent composition or component of the preferred high bulk density: it will be noted, however, that the process also gives good results with compositions containing lower levels of detergent-active material.
For carrying out the process, a mixer is apparently required that combines a high energy stirring input with a cutting action. The Fukae (Trade Mark) FS-G mixer manufactured by Fukae Powtech Kogyo Co., Japan, has been found to give excellent results in batchwise operation.
This apparatus is essentially in the form of a vessel accessible via a top port, provided near its base with a stirrer having a substantially vertical axis, and a cutter . ~........ .
.. , .
. ,....................... ~
200244~
- 9 - C.3285 positioned on a side wall. The stirrer and cutter may be operated independently of one another, and at separately variable speeds.
Other mixers suitable for use in the process include the Diosna ~Trade Mark) V series ex Dierks & S~hne, Germany;
the L~dige (Trade Mark) FM series ex Morton Machine Co.
Ltd., Scotland; and the Pharma Matrix (Trade ~ark) ex T K
Fielder Ltd., England. Other mixers believed to be suitable for use in the process are the Fuji ~Trade Mark) VG-C series ex Fuji Sangyo Co., Japan; the L~dige MTG ex Morton Machine Co. Ltd., Scotland; and the Roto (Trade Mark) ex Zanchetta & Co srl, Italy. The L~dige FM mixer differs from the Fukae mixer mentioned above in that its stirrer has a horizontal axis; this configuration is suitable for continuous operation.
As indicated above, the use of a high speed mixer is essential in the process set out above to effect granulation and densification. Some starting powders require pulverisation before granulation can take place;
whether or not this is necessary depends, among other things, on the method of preparation of the starting powder and its free moisture content. Powders prepared by spray-drying, for example, are more likely to require pulverisation than powders prepared by dry-mixing.
Pulverisation may, if desired, be carried out as a separate process step, in any suitable separate apparatus, before granulation in the high speed mixer is carried out.
It is convenient, however, to use the same high-speed mixer for the pulverisation step as for the granulation step. The high speed mixer may be used for the pulverisation step by running the mixer at high speed, using both stirrer and cutter. A relatively short ,~ , , ' ' ` ~:
;, - 10 - C.3285 residence time (for example, 2-4 minutes for a 35 kg batch) is generally sufficient. A mass of finely divided powder is obtained.
The granulation step follows, and it is during that stage that densification to very high values of at least 650 g/litre, preferably at least 700 g/litre can be achleved, giving a dense, granular product of very uniform particle size and generally spherical particle shape.
The final bulk density can be controlled by choice of residence time, and it has been found that the powder properties of the resulting granulate are best if the bulk density has bee~ allowed to rise to at least 65C g/litre.
The presence of a liquid binder is necessary for successful granulation. The amount of binder added preferably does not exceed that needed to bring the free moisture content of the composition above about 6% by weight, since higher levels lead to a deterioration in the flow properties of the final granulate. If necessary, binder, preferably water, may be added before or during granulation, but some starting powders will inherently contain sufficient moisture. In the Fukae mixer, granulation is effected by running the mixer at a relatively high speed using both stirrer and cutter; a relatively short residence time (for example, 5-8 minutes for a 35 kg batch) is generally sufficient. If a liquid binder is to be added, it may be sprayed in while the mixer is running. In one preferred mode of operation, the mixer is first operated at a relatively slow speed while binder is added, before increasing the speed of the mixer to effect granulation.
If the starting powder has a sufficient free moisture content to render the addition of a binder unnecessary, pulverisation (if required) and granulation need not be .
~ C.3285 regarded as separate process steps but as one single operation. Indeed, it is not, in that case, necessary to decide in advance whether or not pulverisation is r~quired: the mixer may simply be allowed to do what is necessary, since the mixer conditions required are substantially the same for pulverisation and for granulation.
In general, it is highly preferred that during granulation no aagent for improving surface properties" as defined in the above-mentioned JP 61 069897A (Kao) be present. When processing a formulation having a relatively high ratio of aluminosilicate builder to surfactant, in accordance with examples of the present invention, the use of a finely divided particulate material such as fine sodium al~minosilicate during the granulation step is not only unnecessary but can with some formulations make granulation more difficult, or even impossible.
In accordance with a preferred embodiment of the invention, a finely divided particulate flow aid may be admixed with the granular material after granulation is complete. Advantageously, flow aid is added while the granulate is still in the high-speed mixer, and the mixer is operated at a slow speed for a further short period. No further granulation occurs at this stage. It is also within the scope of the invention to add the flaw aid to the granulate after removing the latter to different apparatus.
This embodiment of the invention should be distinguished from the prior art process of JP 61 069897A (Kao), mentioned above, in which an ~agent for improving surface propertiesU~ which can be fine sodium aluminosilicate, is present during the granulation stage itself. It is within the scope of the present invention to add a .
.
' ~ ..
- 12 - C.3285 particulate flow aid after granulation is complete, but, aLs explained above, it is essential to the invention that no finely divided particulate ~agent for improving surface properties" be present during granulation. The addition of a flow aid after granulation is complete can have an additional beneficial effect on the properties of the qranulate, regardless of the formulation, whereas the presence of this type of material during the granulation step in the present process makes processing more difficult.
According to a preferred embodiment of the process, granulation is carried out at a controlled temperature somewhat above ambient, preferably above 30 deg C. The optimum temperature is apparently formulation-dependent, but appears generally to lie within the range of from 30 to 45 deg C, preferably about 35 deg C. This temperature may also be maintained during the subsequent admixture of a flow aid.
The flow aid is a finely divided particulate material. The preferred average particle size is 0.1 to 20 microns, more preferably 1 to 10 microns. Substantially amorphous materials are preferred.
According to a highly preferred embodiment, the flow aid is finely divided amorphous sodium aluminosilicate. This material is effective in improving flow properties even at very low levels, and also has the effect of increasing bulk density. It is therefore possible to adjust bulk density by appropriate choice of the level of amorphous sodium aluminosilicate added after granulation.
A suitable material is available commercially from Crosfield Chemicals Ltd, Warrington, Cheshire, under the trade mark Alusil. Other flow aids manufactured by this : : ' -- :
.. ~ ' . - .
::
- 13 - C.3285 company include Neosyl (Trade Mark) precipitated silica and Microcal (Trade Mark) precipitated calcium silicate.
The flow aid is advantageously used in an amount of from 0~2 to 5.0~ by weight, based on the starting powder, more preferably from 0.5 to 3.0% by weight.
Zeolite (hydrated crystalline sodium aluminosilicate) is substantially less effective as a flow aid in the context of the present invention. Substantially higher levels than those quoted above are needed before any flow or bulk density benefit i8 observed.
The invention is illustrated by the following non-limiting Examples, in which parts and percentages are by weight unless otherwise stated.
Example 1 A detergent composition is prepared to the following composition by spray-drying an aqueous slurry to a free moisture content of substantially zero:
parts Linear alkylbenzene sulphonate 24.0 Nonionic surfactant 2.0 Soap 1.0 Zeolite (anhydr.) 38.0 Water bound with zeolite 10.84 Sodium silicate 4.0 Acrylatetmaleate copolymer 2.0 Minor ingredients 2.0 Sodium carbonate 10.0 94.64 .
, .. ~ .. . ~ .
:, :
.
`- 2002440 - 14 - C.3285 The ratio of zeolite tanhydrous) to non-soap surfactant in this composition is 1.46.
35 kg of this spray-dried powder are introduced into a Fukae (Trade Mark) FS-G series high speed mixer, and pulverised at high speed for 2-4 minutes. Water (2.0 parts) is then sprayed in while the mixer is allowed to run at a slower speed, then the speed is increased for 5-8 minutes while maintaining the temperature at about 35oC.
During this period granulation occurs.
A sample of the granular product is removed from the mixer. It is generally free-flowing and shows no tendency to cake. Its dynamic flow rate can for example be about 65 ml/s.
1.0 part of Alusil (Trade Mark~ fine amorphous sodium aluminosilicate is introduced into the Fukae mixer, which is then operated at a slow speed for 1 minute. The resulting granular product is free-flowing and generally shows no tendency to cake. In representative runs, its bulk density can be about 740 g/litre, its mean particle size about 405 microns and its dynamic flow rate about 105 ml/s.
The following ingredients are then mixed with the granular material to give 99 parts of final detergent powder:
Coloured speckles 1.5 parts Alcalase (TM)) 0.61 parts Lipase to required extent eg 0.5 parts Perfume 0.25 parts (Lipase enzyme is postdosed to the required extent after the main body of preparative steps described).
:
` ' ' ~
, .
. .
- 15 - C.3285 E~amples 2 and 3 35 kg of the spxay-dried powder used in Example 1 are introduced into a Lodige (Trade Mark) FM series high speed mixer, and pulverised for 4 minutes. Water (1.1 kg, 3.5%) is then sprayed in while the mixer continues to run at the same speed, then the mixer is allowed to run for a further 3 minutes while the temperature was maintained at about 35C. During this period granulation occurs~ A sample (Example 2) is removed from the mixer and its powder properties determined: these are for examples as shown in Table 1 below.
Alusil (Trade Mark) finely divided amorphous sodium aluminosilicate (1.2 kg) is then introduced into the mixer which is allowed to run for a further 0.5 minutes.
Physical properties of an example of the resulting powder (Example 3) are shown in Table 1 below, from which the beneficial effect on flow and bulk density of adding a flow aid after granulation is complete is apparent. The presence of the Alusil did result in an increase in the content of fine particles < 180 microns, but not to an unacceptable level.
Table 1 Example 2 3 Bulk density (g/l) 680 754 Dynamic flow rate (mlts) 100 109 Particle size (microns) 573 524 Fines content (wt~ of particles < 180 microns) 0 15 - .: ~. . .
'. :. : , .
.
- 16 - C.328S
_xamples 4 to 6 Three powders are prepared by spray-drying the nominal composition shown in Example 1 to three different moisture contents, as shown in Table 2 below. Since the 38.0 parts of zeolite (anhydrous basis) in the fo~mulation require 10.84 parts of water of hydration, the free moisture content of each powder is found by subtracting that figure from the total moisture content: it will be noted that the powder of Example 4 is overdried, while that of Example 6 contains 3.16 parts of free moisture.
A 10 kg batch of each powder is granulated (and, where necessary, pulverised) in a Diosna (Trade Mark) V series 1~ mixer, using an agitator speed of 196 r p m and a chopper speed of 3000 r p m. In the case of Examples 4 and 5, where pulverisation initially occurred, water is sprayed into the mixer, in the amount and for the time indicated, before granulating. After granulation is complete, Alusil finely divided amorphous sodium aluminosilicate (0.1 kg) is admixed to the granulate. Lipase enzyme is postdosed to the required extent (e.g. 0.5%) after the main body of preparative steps described. Properties of examples of the three granulates are shown in Table 2.
Table 2 Example 4 5 6 Total moisture (wt ~) 8.0 11.0 14.0 Pulverisation time (min) 4 3 ;
~. : , .
- 17 - C.3285 Water addition:
amount (kg) 0.2 0.1 time ~min) 2 Granulation time (min) 4 3 4 Bulk density (g/l) 740 832 735 Dynamic flow rate (ml/s) 114 120 120 Compressibility (% v/v) 8.8 9.4 8.8 Particle size (microns) 483 553 521 Fines content (wt% < 180 5.0 2.4 6.1 microns) Example 7 The effectiveness of lipolytic enzyme in a detergent composition of the type described above, and the comparative effectiveness of lipolytic enzyme in a comparative detergent formulation, was estimated as follows.
(a) Triolein-soiled cotton and polyester materials were washed in a pH-stat under uniform conditions using two detergent formulations as given below.
.- ., ---- .. ~ . . . . - , -.
-: .. ~ .:
~`"~ :. ' ` 2002440 - 18 - C.3285 (b) pH-stat titration of the acidity developed by free fatty acid (FFA) during the wash was carried out to show an index quantity of free fatty acid per standard test cloth indicating the relative effectiveness of lipolytic action.
The detergent formulations were as follows:
(a) (b) ~ %
linear alkylbenzene sulphonate 20 26 coco-PAS - 8 nonionic detergent 2 4 15 soap 1 3 zeolite (anhydrous) 35 18 polymer 1.5 sodium carbonate 10 20 sodium sulphate 11 4 20 sodium silicate 4 6 sodium carboxymethylcellulose 0.75 sodium succinate 2 ratio bl:a 1.59 0.47 Lipase was used in each case in an amount corresponding to 5 LU/ml wash solution, and the wash water had 4 degrees FH
Calcium, 2 degrees F~ magnesium. Wash temperature was 30 degrees C. Cloth:liquor ratio was 1:80, the cotton was soiled with 6.4% by weight triolein and the polyester had 10~ by weight triolein.
After washing with formulation (a) the test showed the presence of 2.3 micromoles of FFA produced in the wash liquor per cotton test cloth and 7.6 micromoles of FFA
per polyester test cloth.
, , ~ . . : .
'' ` ~ ' :' .
- 19 - C.32~5 After washing with comparative formulation (b) the test s~lowed the presence of l.0 micromoles of FFA produced in the wash liquor per cotton test cloth and 6.1 micromoles of ~FA per polyester test cloth.
It was apparent that formulation (a) enabled comparatively more lipolytic activity from the given quantity of lipolytic enzyme.
Example 8 A preferred detergent composition was prepared substantially according to the method of Example 1 but with the following composition:
% by weight Linear alkylbenzene sulphonate 25 Nonionic surfactant (7E0) 2 Soap (fully hardened tallow soap) Zeolite (anhydr.) 36 Water bound with zeolite lO
Alkaline sodium silicate 4 Acrylatetmaleate copolymer CP5 Sodium carbonate 16 Sodium sulphate 2 Na caroxymethylcellulose Enzymes 0.6 Minors and water to lO0 The lipase (preferably Lipolase) is added as described above, and is preferably present in addition to protease (Alcalase).
The invention is susceptible of modifications and variations within the scope of the preceding disclosure . ~ . .
. . ~
- 20 - C.3285 - with Examples, and extends to all combinations and subcombinations of the features mentioned or incorporated.
.
. - ' ' .;....
. ............................ . ...
.
~he lipolytic enzyme can usefully be added in the form of a granular composition of lipolytic enzyme with carrier material.
The added amount of lipolytic enzyme can be chosen within wide limits, for example 30 to 30,000 LU/g of granular detergent composition, e.g. at least 300 LU/g, often usefully at least 500 LU/g, sometimes preferably above 1000 LU/g or above 3000 LU/g or more.
Ihe lipolytic enzyme can be chosen from among a wide range of lipases: in particular the lipases described in for example the following patent specifications, EP 0214761 (Novo), EP 0258068 (Novo) and especially lipases showing immunological cross-reactivity with antisera raised against lipase from Thermomyces lanuginosus ATCC 22070, EP 0205208 (Unilever) and EP 0206390 (Unilever), and especially lipases showing immunological cross-reactivity with antisera raised against lipase with Chromobacter viscosum var lipolyticum NRRL B-3673, or against lipase from Alcaligenes PL-679, ATCC 31371 and FERM-P 3783, also the lipases described in specifications WO 87/00859 (Gist-Brocades) and EP 0204284 (Sapporo Breweries). Suitable in particular are for example the following commercially available lipase preparations: Novo Lipolase, Amano lipases CE, P, B, AP, M-AP, AML, and CES, and Meito lipases MY-30, OF, and PL, also esterase MM, Lipozym, SP225, SP285, Saiken lipase, Enzeco lipase, Toyo Jozo lipase and Diosynth lipase (Trade Marks).
... .
~002440 ~ 5 - C.3285 It has now been surprisingly found that lipolytic enzyme e~erts a comparatively greater effect when used in compositions of the type described above, than when used in comparative compositions as illustrated in the lipolytic example below.
According to preferred embodiments, the invention provides detergent powders combining high bulk density, good powder properties and excellent washing and cleaning performance, that can be prepared easily and conveniently.
These detergent compositions owe their combination of excellent properties and ready processability to a moderate content of surfactant, at least part of which is anionic, and a relatively high level of sodium aluminosilicate builder. It has been found that when the absolute amounts of aluminosilicate builder and surfactant, and the ratio of one to the other, are suitably chosen, the spray-dried base powder may be pulverised and granulated in a high-speed mixer without the need for the use of an "agent for improving surface properties" during the granulation step as prescribed by JP 61 069897A (Kao). The resulting dense granulate has good flow properties and is at least equal in washing and cleaning performance and cold water dispersability to the compositions described in the Kao specification which contain substantially higher levels of surfactant.
The aluminosilicate builder present in the compositions may be crystalline or amorphous or a mixture thereof, and can have the general formula 0.8-1.5 Na20 . A1203 . 0.8-6 SiO2.
- 6 - C.3285 These materials contain some bound water and should in most cases have a calcium ion exchange capacity of at least about 50 mg CaO/g. The preferred aluminosilicates contain 1.5-3.5 SiO2 units (in the formula above) and have a particle size of not more than about 100 microns, preferably not more than about 20 microns. Both amorphous and crystalline aluminosilicates can be made readily by reaction between sodium silicate and sodium aluminate, as amply described in the literatur~.
Crystalline aluminosilicates ~zeolites) are preferred for use in the present invention. Suitable materials are described, for example, in GB 1 473 201 (Henkel) and GB 1 429 143 (Procter & Gamble). The preferred sodium aluminosilicates of this type are the well-known commercially available zeolites A and X, and mixtures thereof. Especially preferred for use in the present invention is Type 4A zeolite.
The ratio of aluminosilicate builder (anhydrous basis) to total non-soap surfactant in the compositions is preferably within the range of from 1.2:1 to 1.3:1.
The non-soap surfactant present consists at least partially of anionic surfactant. Suitable anionic surfactants are well known to those skilled in the art, and include linear alkylbenzene sulphonates, primary alcohol sulphates, alkyl ether sulphates, alpha-olefin sulphonates, internal olefin sulphonates, fatty acid ester sulphonates and combinations thereof.
If desired, nonionic surfactant may also be present, preferably in a minor amount. Suitably the surfactant . . .
- 7 - C.3~85 c:omponent of the compositions of the invention may be - c:onstituted by 10 to 35~ by weight of anionic surfactant and 0 to 10~ by weight of nonionic surfactant.
If desired, soap may also be present, to provide foam control and additional detergency and builder power; soap is not included in the 17 to 35% figure given above for the total surfactant content of the compositions.
The compositions preferably do not contain more than 5~ by weight of phosphate builders, and are more preferably substantially free of phosphate builders.
The particulate starting composition may be prepared by any suitable tower or non-tower method, for example, spray-drying or dry-mixing; spray-drying is preferred.
The final granulate may be used as a complete detergent composition in its own right. Alternatively, additional ingredients such as enzymes, bleach and perfume that are not suitable for undergoing the granulation process and the steps that precede it may be admixed to the granulate to make a final product.
In preferred cases the final granulate has a bulk density of at least 650 g/litre and more preferably at least 700 g/litre. It is preferably also characterised by an especially low particle porosity, not exceeding 25~ and preferably not exceeding 20%, which distinguishes it from even the densest powders prepared by spray-drying alone.
In suitable examples of processes for making the preferred high-bulk-density compositions, a particulate starting material (detergent base powder) prepared by any suitable method is treated in a high-speed mixer to increase its :, ;. . .
- 8 - C.3285 bulk density and simultaneously to improve its powder - properties. The process is especially useful for the densification of a spray-dried powder, and provides a route for the production of very dense granular detergent compositions, having excellent cleaning performance, containing low to moderate levels of anionic surfactant and high levels of aluminosilicate builder.
A preferred starting powder comprises:
(a) from 17 to 35~ by weight of non-soap detergent-active material consisting at least partially of anionic detergent-active material, and (b) from 28 to 45% by weight of crystalline or amorphous sodium aluminosilicate, the weight ratio of (b) to (a) being from 0.9:1 to 2.6:1, and other detergent components to 100~ by weight.
On treatment in a high-speed mixer by an example of the process set out above, this can gives a granular detergent composition or component of the preferred high bulk density: it will be noted, however, that the process also gives good results with compositions containing lower levels of detergent-active material.
For carrying out the process, a mixer is apparently required that combines a high energy stirring input with a cutting action. The Fukae (Trade Mark) FS-G mixer manufactured by Fukae Powtech Kogyo Co., Japan, has been found to give excellent results in batchwise operation.
This apparatus is essentially in the form of a vessel accessible via a top port, provided near its base with a stirrer having a substantially vertical axis, and a cutter . ~........ .
.. , .
. ,....................... ~
200244~
- 9 - C.3285 positioned on a side wall. The stirrer and cutter may be operated independently of one another, and at separately variable speeds.
Other mixers suitable for use in the process include the Diosna ~Trade Mark) V series ex Dierks & S~hne, Germany;
the L~dige (Trade Mark) FM series ex Morton Machine Co.
Ltd., Scotland; and the Pharma Matrix (Trade ~ark) ex T K
Fielder Ltd., England. Other mixers believed to be suitable for use in the process are the Fuji ~Trade Mark) VG-C series ex Fuji Sangyo Co., Japan; the L~dige MTG ex Morton Machine Co. Ltd., Scotland; and the Roto (Trade Mark) ex Zanchetta & Co srl, Italy. The L~dige FM mixer differs from the Fukae mixer mentioned above in that its stirrer has a horizontal axis; this configuration is suitable for continuous operation.
As indicated above, the use of a high speed mixer is essential in the process set out above to effect granulation and densification. Some starting powders require pulverisation before granulation can take place;
whether or not this is necessary depends, among other things, on the method of preparation of the starting powder and its free moisture content. Powders prepared by spray-drying, for example, are more likely to require pulverisation than powders prepared by dry-mixing.
Pulverisation may, if desired, be carried out as a separate process step, in any suitable separate apparatus, before granulation in the high speed mixer is carried out.
It is convenient, however, to use the same high-speed mixer for the pulverisation step as for the granulation step. The high speed mixer may be used for the pulverisation step by running the mixer at high speed, using both stirrer and cutter. A relatively short ,~ , , ' ' ` ~:
;, - 10 - C.3285 residence time (for example, 2-4 minutes for a 35 kg batch) is generally sufficient. A mass of finely divided powder is obtained.
The granulation step follows, and it is during that stage that densification to very high values of at least 650 g/litre, preferably at least 700 g/litre can be achleved, giving a dense, granular product of very uniform particle size and generally spherical particle shape.
The final bulk density can be controlled by choice of residence time, and it has been found that the powder properties of the resulting granulate are best if the bulk density has bee~ allowed to rise to at least 65C g/litre.
The presence of a liquid binder is necessary for successful granulation. The amount of binder added preferably does not exceed that needed to bring the free moisture content of the composition above about 6% by weight, since higher levels lead to a deterioration in the flow properties of the final granulate. If necessary, binder, preferably water, may be added before or during granulation, but some starting powders will inherently contain sufficient moisture. In the Fukae mixer, granulation is effected by running the mixer at a relatively high speed using both stirrer and cutter; a relatively short residence time (for example, 5-8 minutes for a 35 kg batch) is generally sufficient. If a liquid binder is to be added, it may be sprayed in while the mixer is running. In one preferred mode of operation, the mixer is first operated at a relatively slow speed while binder is added, before increasing the speed of the mixer to effect granulation.
If the starting powder has a sufficient free moisture content to render the addition of a binder unnecessary, pulverisation (if required) and granulation need not be .
~ C.3285 regarded as separate process steps but as one single operation. Indeed, it is not, in that case, necessary to decide in advance whether or not pulverisation is r~quired: the mixer may simply be allowed to do what is necessary, since the mixer conditions required are substantially the same for pulverisation and for granulation.
In general, it is highly preferred that during granulation no aagent for improving surface properties" as defined in the above-mentioned JP 61 069897A (Kao) be present. When processing a formulation having a relatively high ratio of aluminosilicate builder to surfactant, in accordance with examples of the present invention, the use of a finely divided particulate material such as fine sodium al~minosilicate during the granulation step is not only unnecessary but can with some formulations make granulation more difficult, or even impossible.
In accordance with a preferred embodiment of the invention, a finely divided particulate flow aid may be admixed with the granular material after granulation is complete. Advantageously, flow aid is added while the granulate is still in the high-speed mixer, and the mixer is operated at a slow speed for a further short period. No further granulation occurs at this stage. It is also within the scope of the invention to add the flaw aid to the granulate after removing the latter to different apparatus.
This embodiment of the invention should be distinguished from the prior art process of JP 61 069897A (Kao), mentioned above, in which an ~agent for improving surface propertiesU~ which can be fine sodium aluminosilicate, is present during the granulation stage itself. It is within the scope of the present invention to add a .
.
' ~ ..
- 12 - C.3285 particulate flow aid after granulation is complete, but, aLs explained above, it is essential to the invention that no finely divided particulate ~agent for improving surface properties" be present during granulation. The addition of a flow aid after granulation is complete can have an additional beneficial effect on the properties of the qranulate, regardless of the formulation, whereas the presence of this type of material during the granulation step in the present process makes processing more difficult.
According to a preferred embodiment of the process, granulation is carried out at a controlled temperature somewhat above ambient, preferably above 30 deg C. The optimum temperature is apparently formulation-dependent, but appears generally to lie within the range of from 30 to 45 deg C, preferably about 35 deg C. This temperature may also be maintained during the subsequent admixture of a flow aid.
The flow aid is a finely divided particulate material. The preferred average particle size is 0.1 to 20 microns, more preferably 1 to 10 microns. Substantially amorphous materials are preferred.
According to a highly preferred embodiment, the flow aid is finely divided amorphous sodium aluminosilicate. This material is effective in improving flow properties even at very low levels, and also has the effect of increasing bulk density. It is therefore possible to adjust bulk density by appropriate choice of the level of amorphous sodium aluminosilicate added after granulation.
A suitable material is available commercially from Crosfield Chemicals Ltd, Warrington, Cheshire, under the trade mark Alusil. Other flow aids manufactured by this : : ' -- :
.. ~ ' . - .
::
- 13 - C.3285 company include Neosyl (Trade Mark) precipitated silica and Microcal (Trade Mark) precipitated calcium silicate.
The flow aid is advantageously used in an amount of from 0~2 to 5.0~ by weight, based on the starting powder, more preferably from 0.5 to 3.0% by weight.
Zeolite (hydrated crystalline sodium aluminosilicate) is substantially less effective as a flow aid in the context of the present invention. Substantially higher levels than those quoted above are needed before any flow or bulk density benefit i8 observed.
The invention is illustrated by the following non-limiting Examples, in which parts and percentages are by weight unless otherwise stated.
Example 1 A detergent composition is prepared to the following composition by spray-drying an aqueous slurry to a free moisture content of substantially zero:
parts Linear alkylbenzene sulphonate 24.0 Nonionic surfactant 2.0 Soap 1.0 Zeolite (anhydr.) 38.0 Water bound with zeolite 10.84 Sodium silicate 4.0 Acrylatetmaleate copolymer 2.0 Minor ingredients 2.0 Sodium carbonate 10.0 94.64 .
, .. ~ .. . ~ .
:, :
.
`- 2002440 - 14 - C.3285 The ratio of zeolite tanhydrous) to non-soap surfactant in this composition is 1.46.
35 kg of this spray-dried powder are introduced into a Fukae (Trade Mark) FS-G series high speed mixer, and pulverised at high speed for 2-4 minutes. Water (2.0 parts) is then sprayed in while the mixer is allowed to run at a slower speed, then the speed is increased for 5-8 minutes while maintaining the temperature at about 35oC.
During this period granulation occurs.
A sample of the granular product is removed from the mixer. It is generally free-flowing and shows no tendency to cake. Its dynamic flow rate can for example be about 65 ml/s.
1.0 part of Alusil (Trade Mark~ fine amorphous sodium aluminosilicate is introduced into the Fukae mixer, which is then operated at a slow speed for 1 minute. The resulting granular product is free-flowing and generally shows no tendency to cake. In representative runs, its bulk density can be about 740 g/litre, its mean particle size about 405 microns and its dynamic flow rate about 105 ml/s.
The following ingredients are then mixed with the granular material to give 99 parts of final detergent powder:
Coloured speckles 1.5 parts Alcalase (TM)) 0.61 parts Lipase to required extent eg 0.5 parts Perfume 0.25 parts (Lipase enzyme is postdosed to the required extent after the main body of preparative steps described).
:
` ' ' ~
, .
. .
- 15 - C.3285 E~amples 2 and 3 35 kg of the spxay-dried powder used in Example 1 are introduced into a Lodige (Trade Mark) FM series high speed mixer, and pulverised for 4 minutes. Water (1.1 kg, 3.5%) is then sprayed in while the mixer continues to run at the same speed, then the mixer is allowed to run for a further 3 minutes while the temperature was maintained at about 35C. During this period granulation occurs~ A sample (Example 2) is removed from the mixer and its powder properties determined: these are for examples as shown in Table 1 below.
Alusil (Trade Mark) finely divided amorphous sodium aluminosilicate (1.2 kg) is then introduced into the mixer which is allowed to run for a further 0.5 minutes.
Physical properties of an example of the resulting powder (Example 3) are shown in Table 1 below, from which the beneficial effect on flow and bulk density of adding a flow aid after granulation is complete is apparent. The presence of the Alusil did result in an increase in the content of fine particles < 180 microns, but not to an unacceptable level.
Table 1 Example 2 3 Bulk density (g/l) 680 754 Dynamic flow rate (mlts) 100 109 Particle size (microns) 573 524 Fines content (wt~ of particles < 180 microns) 0 15 - .: ~. . .
'. :. : , .
.
- 16 - C.328S
_xamples 4 to 6 Three powders are prepared by spray-drying the nominal composition shown in Example 1 to three different moisture contents, as shown in Table 2 below. Since the 38.0 parts of zeolite (anhydrous basis) in the fo~mulation require 10.84 parts of water of hydration, the free moisture content of each powder is found by subtracting that figure from the total moisture content: it will be noted that the powder of Example 4 is overdried, while that of Example 6 contains 3.16 parts of free moisture.
A 10 kg batch of each powder is granulated (and, where necessary, pulverised) in a Diosna (Trade Mark) V series 1~ mixer, using an agitator speed of 196 r p m and a chopper speed of 3000 r p m. In the case of Examples 4 and 5, where pulverisation initially occurred, water is sprayed into the mixer, in the amount and for the time indicated, before granulating. After granulation is complete, Alusil finely divided amorphous sodium aluminosilicate (0.1 kg) is admixed to the granulate. Lipase enzyme is postdosed to the required extent (e.g. 0.5%) after the main body of preparative steps described. Properties of examples of the three granulates are shown in Table 2.
Table 2 Example 4 5 6 Total moisture (wt ~) 8.0 11.0 14.0 Pulverisation time (min) 4 3 ;
~. : , .
- 17 - C.3285 Water addition:
amount (kg) 0.2 0.1 time ~min) 2 Granulation time (min) 4 3 4 Bulk density (g/l) 740 832 735 Dynamic flow rate (ml/s) 114 120 120 Compressibility (% v/v) 8.8 9.4 8.8 Particle size (microns) 483 553 521 Fines content (wt% < 180 5.0 2.4 6.1 microns) Example 7 The effectiveness of lipolytic enzyme in a detergent composition of the type described above, and the comparative effectiveness of lipolytic enzyme in a comparative detergent formulation, was estimated as follows.
(a) Triolein-soiled cotton and polyester materials were washed in a pH-stat under uniform conditions using two detergent formulations as given below.
.- ., ---- .. ~ . . . . - , -.
-: .. ~ .:
~`"~ :. ' ` 2002440 - 18 - C.3285 (b) pH-stat titration of the acidity developed by free fatty acid (FFA) during the wash was carried out to show an index quantity of free fatty acid per standard test cloth indicating the relative effectiveness of lipolytic action.
The detergent formulations were as follows:
(a) (b) ~ %
linear alkylbenzene sulphonate 20 26 coco-PAS - 8 nonionic detergent 2 4 15 soap 1 3 zeolite (anhydrous) 35 18 polymer 1.5 sodium carbonate 10 20 sodium sulphate 11 4 20 sodium silicate 4 6 sodium carboxymethylcellulose 0.75 sodium succinate 2 ratio bl:a 1.59 0.47 Lipase was used in each case in an amount corresponding to 5 LU/ml wash solution, and the wash water had 4 degrees FH
Calcium, 2 degrees F~ magnesium. Wash temperature was 30 degrees C. Cloth:liquor ratio was 1:80, the cotton was soiled with 6.4% by weight triolein and the polyester had 10~ by weight triolein.
After washing with formulation (a) the test showed the presence of 2.3 micromoles of FFA produced in the wash liquor per cotton test cloth and 7.6 micromoles of FFA
per polyester test cloth.
, , ~ . . : .
'' ` ~ ' :' .
- 19 - C.32~5 After washing with comparative formulation (b) the test s~lowed the presence of l.0 micromoles of FFA produced in the wash liquor per cotton test cloth and 6.1 micromoles of ~FA per polyester test cloth.
It was apparent that formulation (a) enabled comparatively more lipolytic activity from the given quantity of lipolytic enzyme.
Example 8 A preferred detergent composition was prepared substantially according to the method of Example 1 but with the following composition:
% by weight Linear alkylbenzene sulphonate 25 Nonionic surfactant (7E0) 2 Soap (fully hardened tallow soap) Zeolite (anhydr.) 36 Water bound with zeolite lO
Alkaline sodium silicate 4 Acrylatetmaleate copolymer CP5 Sodium carbonate 16 Sodium sulphate 2 Na caroxymethylcellulose Enzymes 0.6 Minors and water to lO0 The lipase (preferably Lipolase) is added as described above, and is preferably present in addition to protease (Alcalase).
The invention is susceptible of modifications and variations within the scope of the preceding disclosure . ~ . .
. . ~
- 20 - C.3285 - with Examples, and extends to all combinations and subcombinations of the features mentioned or incorporated.
.
. - ' ' .;....
. ............................ . ...
.
Claims (9)
1. A granular detergent composition or component therefor, which comprises:
(a) from 6% to 35% by weight of non-soap detergent-active material consisting at least partially of anionic and/or nonionic active material;
(b) at least 45% by weight of builder, (b1) the builder including at least 28% by weight (anhydrous basis) of crystalline or amorphous sodium aluminosilicate and/or citrate, carbonate, or layered silicate builder, (c) a lipolytic enzyme, the weight ratio of (b1) to (a) being from 0.9:1 to 2.6:1, preferably from 1.2:1 to 1.8:1; and other detergent ingredients to 100% by weight.
(a) from 6% to 35% by weight of non-soap detergent-active material consisting at least partially of anionic and/or nonionic active material;
(b) at least 45% by weight of builder, (b1) the builder including at least 28% by weight (anhydrous basis) of crystalline or amorphous sodium aluminosilicate and/or citrate, carbonate, or layered silicate builder, (c) a lipolytic enzyme, the weight ratio of (b1) to (a) being from 0.9:1 to 2.6:1, preferably from 1.2:1 to 1.8:1; and other detergent ingredients to 100% by weight.
2. A composition as claimed in claim 1, which has been prepared by treating a particulate starting material comprising: (a) from 5 to 35% by weight of non-soap detergent-active material consisting at least partially of anionic detergent-active material, and (b) from 28 to 45 by weight (Anhydrous basis) of crystalline or amorphous sodium aluminosilicate, the weight ratio of (b) to (a) being at least 1.9:1, and other detergent components to 100% by weight in a high-speed mixer in the presence of a liquid binder but in the absence of a finely dividied particulate agent for improving surface properties, whereby granulation and densification to a bulk density of at least 650 g/litre are effected, and adding a lipolytic enzyme preparation after the granulation state which has been carried out in the high-speed mixer.
3. A composition as claimed in claim 1 or 2, which has a bulk density of at least 650 g/litre.
4. A composition as claimed in claim 1, 2 or 3, in which the lipolytic enzyme is Lipolase (TM).
5. A composition as claimed in any of claims 1-4, in which the lipolytic enzyme is present at from about 300-3000 LU/g.
6. A composition as claimed in any of claims 1-5, in which the proportion of non-soap detergent-active material is over 17% by weight.
7. A composition as claimed in any of claims 1-6, in which the builder includes 28-45% by weight of component (b1).
8. A detergent composition substantially as described in relation to any one of the foregoing Examples.
9. The detergent composition as claimed in claim 1 and substantially as described herein.
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
GB888826110A GB8826110D0 (en) | 1988-11-08 | 1988-11-08 | Enzyme-containing detergent compositions |
GB8826110.2 | 1988-11-08 |
Publications (1)
Publication Number | Publication Date |
---|---|
CA2002440A1 true CA2002440A1 (en) | 1990-05-08 |
Family
ID=10646480
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
CA 2002440 Abandoned CA2002440A1 (en) | 1988-11-08 | 1989-11-07 | Enzyme-containing detergent compositions |
Country Status (6)
Country | Link |
---|---|
EP (1) | EP0368589A3 (en) |
JP (1) | JPH02187500A (en) |
AU (1) | AU4446389A (en) |
BR (1) | BR8905726A (en) |
CA (1) | CA2002440A1 (en) |
GB (1) | GB8826110D0 (en) |
Families Citing this family (11)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
GB8828955D0 (en) * | 1988-12-12 | 1989-01-25 | Unilever Plc | Enzyme-containing detergent compositions and their use |
DE4034131C2 (en) * | 1990-10-26 | 1999-08-26 | Henkel Kgaa | Builders for detergents |
EP0495257B1 (en) * | 1991-01-16 | 2002-06-12 | The Procter & Gamble Company | Compact detergent compositions with high activity cellulase |
US5443750A (en) * | 1991-01-16 | 1995-08-22 | The Procter & Gamble Company | Detergent compositions with high activity cellulase and softening clays |
AU2473592A (en) * | 1991-08-21 | 1993-03-16 | Procter & Gamble Company, The | Detergent compositions containing lipase and terpene |
JPH07506618A (en) * | 1992-05-08 | 1995-07-20 | ザ、プロクター、エンド、ギャンブル、カンパニー | Granular detergent composition containing lipase |
AU6267694A (en) * | 1993-02-26 | 1994-09-14 | Procter & Gamble Company, The | High active enzyme granulates |
DE4313949A1 (en) * | 1993-04-28 | 1994-11-03 | Henkel Kgaa | Powder detergent with an ecologically harmless builder system, special surfactant combination and lipase |
DE4411349A1 (en) * | 1994-03-31 | 1995-10-05 | Henkel Kgaa | Textile detergent containing lipase |
EP0912682A1 (en) * | 1996-05-15 | 1999-05-06 | The Procter & Gamble Company | Detergent compositions comprising specific lipolytic enzyme and a specific surfactant system |
WO1997043380A1 (en) * | 1996-05-15 | 1997-11-20 | The Procter & Gamble Company | Detergent compositions comprising specific lipolytic enzyme and zeolite map |
Family Cites Families (6)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPS6169897A (en) * | 1984-09-14 | 1986-04-10 | 花王株式会社 | Production of high density detergent improved in flowability |
GB8514707D0 (en) * | 1985-06-11 | 1985-07-10 | Unilever Plc | Enzymatic detergent composition |
GB8629535D0 (en) * | 1986-12-10 | 1987-01-21 | Unilever Plc | Enzymatic detergent composition |
JPS63305198A (en) * | 1987-06-05 | 1988-12-13 | Kuraray Co Ltd | Enzyme-containing detergent composition |
JP2608047B2 (en) * | 1988-04-11 | 1997-05-07 | ライオン株式会社 | Detergent composition |
GB8810193D0 (en) * | 1988-04-29 | 1988-06-02 | Unilever Plc | Detergent compositions & process for preparing them |
-
1988
- 1988-11-08 GB GB888826110A patent/GB8826110D0/en active Pending
-
1989
- 1989-11-06 AU AU44463/89A patent/AU4446389A/en not_active Abandoned
- 1989-11-06 EP EP19890311465 patent/EP0368589A3/en not_active Withdrawn
- 1989-11-07 CA CA 2002440 patent/CA2002440A1/en not_active Abandoned
- 1989-11-08 BR BR8905726A patent/BR8905726A/en unknown
- 1989-11-08 JP JP29095089A patent/JPH02187500A/en active Pending
Also Published As
Publication number | Publication date |
---|---|
GB8826110D0 (en) | 1988-12-14 |
BR8905726A (en) | 1990-06-05 |
EP0368589A3 (en) | 1990-10-31 |
JPH02187500A (en) | 1990-07-23 |
AU4446389A (en) | 1990-05-17 |
EP0368589A2 (en) | 1990-05-16 |
Similar Documents
Publication | Publication Date | Title |
---|---|---|
CA1336668C (en) | Detergent compositions and process for preparing them | |
EP0351937B2 (en) | Detergent compositions and process for preparing them | |
EP1726636B2 (en) | Detergent Compositions | |
AU611555B2 (en) | Process for preparing detergent compositions | |
AU2006217505A1 (en) | Detergent compositions | |
JPH09509204A (en) | Detergent containing an amorphous silicate builder substance | |
CA2028204A1 (en) | Detergent compositions | |
CA2002440A1 (en) | Enzyme-containing detergent compositions | |
EP1712610B1 (en) | Detergent Compositions | |
US5798327A (en) | Enzymatic detergent compositions | |
US5877139A (en) | Enzymatic detergent compositions | |
CA2008948A1 (en) | Particulate detergent compositions and their use | |
EP0518576B1 (en) | High bulk density granular detergent compositions | |
EP0430328B1 (en) | Process for preparing high bulk density detergent powders containing clay | |
CA2005022C (en) | Enzyme-containing detergent compositions and their use | |
CA2376227A1 (en) | Particulate detergent composition containing zeolite | |
KR950013919B1 (en) | Detergent composition | |
EP1712611B1 (en) | Detergent compositions | |
EP0802969B1 (en) | Detergent composition comprising zeolite and amylase enzyme | |
CA2210646C (en) | Detergent composition comprising zeolite map and amylase enzymes | |
GB2296919A (en) | Detergent composition | |
MXPA98002408A (en) | Deterge composition | |
MXPA98002501A (en) | Detergent composition containing a zeolite detergent improvement and a lubricant for elmi | |
AU1134800A (en) | Process for the production of a detergent composition |
Legal Events
Date | Code | Title | Description |
---|---|---|---|
EEER | Examination request | ||
FZDE | Dead |