EP1299511B1 - Granular detergent composition having an improved solubility - Google Patents
Granular detergent composition having an improved solubility Download PDFInfo
- Publication number
- EP1299511B1 EP1299511B1 EP00948658A EP00948658A EP1299511B1 EP 1299511 B1 EP1299511 B1 EP 1299511B1 EP 00948658 A EP00948658 A EP 00948658A EP 00948658 A EP00948658 A EP 00948658A EP 1299511 B1 EP1299511 B1 EP 1299511B1
- Authority
- EP
- European Patent Office
- Prior art keywords
- detergent composition
- granular detergent
- hydrotrope
- surfactant
- sulphonate
- 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
- 239000003599 detergent Substances 0.000 title claims abstract description 80
- 239000000203 mixture Substances 0.000 title claims abstract description 67
- 239000004094 surface-active agent Substances 0.000 claims abstract description 49
- 125000000129 anionic group Chemical group 0.000 claims abstract description 39
- JXLHNMVSKXFWAO-UHFFFAOYSA-N azane;7-fluoro-2,1,3-benzoxadiazole-4-sulfonic acid Chemical compound N.OS(=O)(=O)C1=CC=C(F)C2=NON=C12 JXLHNMVSKXFWAO-UHFFFAOYSA-N 0.000 claims abstract description 38
- 239000003752 hydrotrope Substances 0.000 claims abstract description 31
- QUCDWLYKDRVKMI-UHFFFAOYSA-M sodium;3,4-dimethylbenzenesulfonate Chemical compound [Na+].CC1=CC=C(S([O-])(=O)=O)C=C1C QUCDWLYKDRVKMI-UHFFFAOYSA-M 0.000 claims abstract description 28
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 claims abstract description 19
- 239000003093 cationic surfactant Substances 0.000 claims abstract description 18
- 239000008187 granular material Substances 0.000 claims abstract description 17
- QAOWNCQODCNURD-UHFFFAOYSA-L Sulfate Chemical compound [O-]S([O-])(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-L 0.000 claims abstract description 6
- 229910021653 sulphate ion Inorganic materials 0.000 claims abstract description 6
- 238000004519 manufacturing process Methods 0.000 claims abstract 2
- 239000011248 coating agent Substances 0.000 claims description 29
- 238000000576 coating method Methods 0.000 claims description 29
- 239000002245 particle Substances 0.000 claims description 20
- 239000000463 material Substances 0.000 claims description 14
- 239000004615 ingredient Substances 0.000 claims description 12
- 229920001223 polyethylene glycol Polymers 0.000 claims description 5
- 125000000217 alkyl group Chemical group 0.000 claims description 4
- 238000001035 drying Methods 0.000 claims description 3
- 229920001451 polypropylene glycol Polymers 0.000 claims description 3
- 238000002156 mixing Methods 0.000 claims description 2
- GIPRGFRQMWSHAK-UHFFFAOYSA-M sodium;2-propan-2-ylbenzenesulfonate Chemical compound [Na+].CC(C)C1=CC=CC=C1S([O-])(=O)=O GIPRGFRQMWSHAK-UHFFFAOYSA-M 0.000 claims description 2
- KVCGISUBCHHTDD-UHFFFAOYSA-M sodium;4-methylbenzenesulfonate Chemical compound [Na+].CC1=CC=C(S([O-])(=O)=O)C=C1 KVCGISUBCHHTDD-UHFFFAOYSA-M 0.000 claims 1
- 239000002195 soluble material Substances 0.000 abstract 1
- 238000000034 method Methods 0.000 description 14
- 238000005406 washing Methods 0.000 description 11
- 238000004140 cleaning Methods 0.000 description 9
- -1 alcohol amine Chemical class 0.000 description 8
- 239000000047 product Substances 0.000 description 7
- 238000001694 spray drying Methods 0.000 description 6
- 229910052708 sodium Inorganic materials 0.000 description 5
- 239000011734 sodium Substances 0.000 description 5
- PEDCQBHIVMGVHV-UHFFFAOYSA-N Glycerol Natural products OCC(O)CO PEDCQBHIVMGVHV-UHFFFAOYSA-N 0.000 description 4
- 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 4
- CDBYLPFSWZWCQE-UHFFFAOYSA-L Sodium Carbonate Chemical compound [Na+].[Na+].[O-]C([O-])=O CDBYLPFSWZWCQE-UHFFFAOYSA-L 0.000 description 4
- 238000005054 agglomeration Methods 0.000 description 4
- 230000002776 aggregation Effects 0.000 description 4
- 238000004090 dissolution Methods 0.000 description 4
- 125000001453 quaternary ammonium group Chemical group 0.000 description 4
- 125000001273 sulfonato group Chemical group [O-]S(*)(=O)=O 0.000 description 4
- ZLMJMSJWJFRBEC-UHFFFAOYSA-N Potassium Chemical compound [K] ZLMJMSJWJFRBEC-UHFFFAOYSA-N 0.000 description 3
- 239000002253 acid Substances 0.000 description 3
- 150000007513 acids Chemical class 0.000 description 3
- 150000004996 alkyl benzenes Chemical class 0.000 description 3
- 239000007844 bleaching agent Substances 0.000 description 3
- 239000010419 fine particle Substances 0.000 description 3
- 239000012530 fluid Substances 0.000 description 3
- 150000002500 ions Chemical class 0.000 description 3
- 239000007788 liquid Substances 0.000 description 3
- 229910052700 potassium Inorganic materials 0.000 description 3
- 239000011591 potassium Substances 0.000 description 3
- 239000002689 soil Substances 0.000 description 3
- 239000002202 Polyethylene glycol Substances 0.000 description 2
- GWEVSGVZZGPLCZ-UHFFFAOYSA-N Titan oxide Chemical compound O=[Ti]=O GWEVSGVZZGPLCZ-UHFFFAOYSA-N 0.000 description 2
- 239000012190 activator Substances 0.000 description 2
- 230000015572 biosynthetic process Effects 0.000 description 2
- 150000001768 cations Chemical class 0.000 description 2
- 239000003795 chemical substances by application Substances 0.000 description 2
- 239000000975 dye Substances 0.000 description 2
- 239000000945 filler Substances 0.000 description 2
- 238000000227 grinding Methods 0.000 description 2
- 239000000693 micelle Substances 0.000 description 2
- 239000002736 nonionic surfactant Substances 0.000 description 2
- JRZJOMJEPLMPRA-UHFFFAOYSA-N olefin Natural products CCCCCCCC=C JRZJOMJEPLMPRA-UHFFFAOYSA-N 0.000 description 2
- 239000002304 perfume Substances 0.000 description 2
- 239000000049 pigment Substances 0.000 description 2
- 238000010298 pulverizing process Methods 0.000 description 2
- 150000003839 salts Chemical class 0.000 description 2
- 229910000029 sodium carbonate Inorganic materials 0.000 description 2
- 230000003068 static effect Effects 0.000 description 2
- BDHFUVZGWQCTTF-UHFFFAOYSA-N sulfonic acid Chemical compound OS(=O)=O BDHFUVZGWQCTTF-UHFFFAOYSA-N 0.000 description 2
- 239000010457 zeolite Substances 0.000 description 2
- HZAXFHJVJLSVMW-UHFFFAOYSA-N 2-Aminoethan-1-ol Chemical compound NCCO HZAXFHJVJLSVMW-UHFFFAOYSA-N 0.000 description 1
- MHKLKWCYGIBEQF-UHFFFAOYSA-N 4-(1,3-benzothiazol-2-ylsulfanyl)morpholine Chemical compound C1COCCN1SC1=NC2=CC=CC=C2S1 MHKLKWCYGIBEQF-UHFFFAOYSA-N 0.000 description 1
- QGZKDVFQNNGYKY-UHFFFAOYSA-O Ammonium Chemical compound [NH4+] QGZKDVFQNNGYKY-UHFFFAOYSA-O 0.000 description 1
- CPELXLSAUQHCOX-UHFFFAOYSA-M Bromide Chemical compound [Br-] CPELXLSAUQHCOX-UHFFFAOYSA-M 0.000 description 1
- 125000006539 C12 alkyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])* 0.000 description 1
- GAWIXWVDTYZWAW-UHFFFAOYSA-N C[CH]O Chemical group C[CH]O GAWIXWVDTYZWAW-UHFFFAOYSA-N 0.000 description 1
- OYPRJOBELJOOCE-UHFFFAOYSA-N Calcium Chemical compound [Ca] OYPRJOBELJOOCE-UHFFFAOYSA-N 0.000 description 1
- VEXZGXHMUGYJMC-UHFFFAOYSA-M Chloride anion Chemical compound [Cl-] VEXZGXHMUGYJMC-UHFFFAOYSA-M 0.000 description 1
- 102000004190 Enzymes Human genes 0.000 description 1
- 108090000790 Enzymes Proteins 0.000 description 1
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 1
- FYYHWMGAXLPEAU-UHFFFAOYSA-N Magnesium Chemical compound [Mg] FYYHWMGAXLPEAU-UHFFFAOYSA-N 0.000 description 1
- BPQQTUXANYXVAA-UHFFFAOYSA-N Orthosilicate Chemical compound [O-][Si]([O-])([O-])[O-] BPQQTUXANYXVAA-UHFFFAOYSA-N 0.000 description 1
- 108091005804 Peptidases Proteins 0.000 description 1
- 239000004365 Protease Substances 0.000 description 1
- 102100037486 Reverse transcriptase/ribonuclease H Human genes 0.000 description 1
- PMZURENOXWZQFD-UHFFFAOYSA-L Sodium Sulfate Chemical compound [Na+].[Na+].[O-]S([O-])(=O)=O PMZURENOXWZQFD-UHFFFAOYSA-L 0.000 description 1
- 229910021536 Zeolite Inorganic materials 0.000 description 1
- 150000001298 alcohols Chemical class 0.000 description 1
- 229910052783 alkali metal Inorganic materials 0.000 description 1
- 150000001340 alkali metals Chemical class 0.000 description 1
- 229910052784 alkaline earth metal Inorganic materials 0.000 description 1
- 150000001342 alkaline earth metals Chemical class 0.000 description 1
- 150000003973 alkyl amines Chemical class 0.000 description 1
- 150000001412 amines Chemical class 0.000 description 1
- 150000003863 ammonium salts Chemical class 0.000 description 1
- 150000001450 anions Chemical group 0.000 description 1
- 150000004945 aromatic hydrocarbons Chemical class 0.000 description 1
- IRERQBUNZFJFGC-UHFFFAOYSA-L azure blue Chemical compound [Na+].[Na+].[Na+].[Na+].[Na+].[Na+].[Na+].[Na+].[Al+3].[Al+3].[Al+3].[Al+3].[Al+3].[Al+3].[S-]S[S-].[O-][Si]([O-])([O-])[O-].[O-][Si]([O-])([O-])[O-].[O-][Si]([O-])([O-])[O-].[O-][Si]([O-])([O-])[O-].[O-][Si]([O-])([O-])[O-].[O-][Si]([O-])([O-])[O-] IRERQBUNZFJFGC-UHFFFAOYSA-L 0.000 description 1
- 229910052791 calcium Inorganic materials 0.000 description 1
- 239000011575 calcium Substances 0.000 description 1
- 150000004649 carbonic acid derivatives Chemical class 0.000 description 1
- OEYIOHPDSNJKLS-UHFFFAOYSA-N choline Chemical group C[N+](C)(C)CCO OEYIOHPDSNJKLS-UHFFFAOYSA-N 0.000 description 1
- 150000001860 citric acid derivatives Chemical class 0.000 description 1
- 235000019864 coconut oil Nutrition 0.000 description 1
- 239000003240 coconut oil Substances 0.000 description 1
- 239000000084 colloidal system Substances 0.000 description 1
- 230000000052 comparative effect Effects 0.000 description 1
- 229920001577 copolymer Polymers 0.000 description 1
- 229910000365 copper sulfate Inorganic materials 0.000 description 1
- ARUVKPQLZAKDPS-UHFFFAOYSA-L copper(II) sulfate Chemical compound [Cu+2].[O-][S+2]([O-])([O-])[O-] ARUVKPQLZAKDPS-UHFFFAOYSA-L 0.000 description 1
- 125000002704 decyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])* 0.000 description 1
- 235000014113 dietary fatty acids Nutrition 0.000 description 1
- HNPSIPDUKPIQMN-UHFFFAOYSA-N dioxosilane;oxo(oxoalumanyloxy)alumane Chemical compound O=[Si]=O.O=[Al]O[Al]=O HNPSIPDUKPIQMN-UHFFFAOYSA-N 0.000 description 1
- VTIIJXUACCWYHX-UHFFFAOYSA-L disodium;carboxylatooxy carbonate Chemical compound [Na+].[Na+].[O-]C(=O)OOC([O-])=O VTIIJXUACCWYHX-UHFFFAOYSA-L 0.000 description 1
- 239000003623 enhancer Substances 0.000 description 1
- 239000002979 fabric softener Substances 0.000 description 1
- 239000000194 fatty acid Substances 0.000 description 1
- 229930195729 fatty acid Natural products 0.000 description 1
- 125000001183 hydrocarbyl group Chemical group 0.000 description 1
- 229910052739 hydrogen Inorganic materials 0.000 description 1
- 239000001257 hydrogen Substances 0.000 description 1
- 125000004435 hydrogen atom Chemical class [H]* 0.000 description 1
- 238000004900 laundering Methods 0.000 description 1
- 229910052749 magnesium Inorganic materials 0.000 description 1
- 239000011777 magnesium Substances 0.000 description 1
- 239000011976 maleic acid Substances 0.000 description 1
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 description 1
- 239000010445 mica Substances 0.000 description 1
- 229910052618 mica group Inorganic materials 0.000 description 1
- 125000002347 octyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 description 1
- 230000003287 optical effect Effects 0.000 description 1
- 235000014366 other mixer Nutrition 0.000 description 1
- 229940055076 parasympathomimetics choline ester Drugs 0.000 description 1
- 230000035515 penetration Effects 0.000 description 1
- XAEFZNCEHLXOMS-UHFFFAOYSA-M potassium benzoate Chemical compound [K+].[O-]C(=O)C1=CC=CC=C1 XAEFZNCEHLXOMS-UHFFFAOYSA-M 0.000 description 1
- 239000002244 precipitate Substances 0.000 description 1
- 150000004760 silicates Chemical class 0.000 description 1
- QSKQNALVHFTOQX-UHFFFAOYSA-M sodium nonanoyloxybenzenesulfonate Chemical compound [Na+].CCCCCCCCC(=O)OC1=CC=CC=C1S([O-])(=O)=O QSKQNALVHFTOQX-UHFFFAOYSA-M 0.000 description 1
- 229940045872 sodium percarbonate Drugs 0.000 description 1
- 229910052938 sodium sulfate Inorganic materials 0.000 description 1
- 235000011152 sodium sulphate Nutrition 0.000 description 1
- YNBRSWNUNPAQOF-UHFFFAOYSA-M sodium;phenylmethanesulfonate Chemical class [Na+].[O-]S(=O)(=O)CC1=CC=CC=C1 YNBRSWNUNPAQOF-UHFFFAOYSA-M 0.000 description 1
- 239000007787 solid Substances 0.000 description 1
- 238000005507 spraying Methods 0.000 description 1
- 239000000126 substance Substances 0.000 description 1
- 239000003760 tallow Substances 0.000 description 1
- 239000004408 titanium dioxide Substances 0.000 description 1
- 235000013799 ultramarine blue Nutrition 0.000 description 1
- 239000008096 xylene Substances 0.000 description 1
- VIFYIFQGOLPNHA-UHFFFAOYSA-L zinc;dioxido-oxo-sulfanylidene-$l^{6}-sulfane Chemical compound [Zn+2].[O-]S([O-])(=O)=S VIFYIFQGOLPNHA-UHFFFAOYSA-L 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
- C11D3/16—Organic compounds
- C11D3/34—Organic compounds containing sulfur
- C11D3/3418—Toluene -, xylene -, cumene -, benzene - or naphthalene sulfonates or sulfates
-
- 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
- C11D1/00—Detergent compositions based essentially on surface-active compounds; Use of these compounds as a detergent
- C11D1/38—Cationic compounds
- C11D1/65—Mixtures of anionic with cationic compounds
-
- 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
-
- C—CHEMISTRY; METALLURGY
- C11—ANIMAL OR VEGETABLE OILS, FATS, FATTY SUBSTANCES OR WAXES; FATTY ACIDS THEREFROM; DETERGENTS; CANDLES
- C11D—DETERGENT COMPOSITIONS; USE OF SINGLE SUBSTANCES AS DETERGENTS; SOAP OR SOAP-MAKING; RESIN SOAPS; RECOVERY OF GLYCEROL
- C11D17/00—Detergent materials or soaps characterised by their shape or physical properties
- C11D17/0039—Coated compositions or coated components in the compositions, (micro)capsules
-
- 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
- C11D1/00—Detergent compositions based essentially on surface-active compounds; Use of these compounds as a detergent
- C11D1/02—Anionic compounds
- C11D1/12—Sulfonic acids or sulfuric acid esters; Salts thereof
- C11D1/123—Sulfonic acids or sulfuric acid esters; Salts thereof derived from carboxylic acids, e.g. sulfosuccinates
-
- 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
- C11D1/00—Detergent compositions based essentially on surface-active compounds; Use of these compounds as a detergent
- C11D1/02—Anionic compounds
- C11D1/12—Sulfonic acids or sulfuric acid esters; Salts thereof
- C11D1/14—Sulfonic acids or sulfuric acid esters; Salts thereof derived from aliphatic hydrocarbons or mono-alcohols
- C11D1/143—Sulfonic acid esters
-
- 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
- C11D1/00—Detergent compositions based essentially on surface-active compounds; Use of these compounds as a detergent
- C11D1/02—Anionic compounds
- C11D1/12—Sulfonic acids or sulfuric acid esters; Salts thereof
- C11D1/22—Sulfonic acids or sulfuric acid esters; Salts thereof derived from aromatic compounds
-
- 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
- C11D1/00—Detergent compositions based essentially on surface-active compounds; Use of these compounds as a detergent
- C11D1/02—Anionic compounds
- C11D1/12—Sulfonic acids or sulfuric acid esters; Salts thereof
- C11D1/22—Sulfonic acids or sulfuric acid esters; Salts thereof derived from aromatic compounds
- C11D1/24—Sulfonic acids or sulfuric acid esters; Salts thereof derived from aromatic compounds containing ester or ether groups directly attached to the nucleus
-
- 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
- C11D1/00—Detergent compositions based essentially on surface-active compounds; Use of these compounds as a detergent
- C11D1/02—Anionic compounds
- C11D1/12—Sulfonic acids or sulfuric acid esters; Salts thereof
- C11D1/28—Sulfonation products derived from fatty acids or their derivatives, e.g. esters, amides
-
- 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
- C11D1/00—Detergent compositions based essentially on surface-active compounds; Use of these compounds as a detergent
- C11D1/38—Cationic compounds
- C11D1/62—Quaternary ammonium compounds
Definitions
- the present invention relates to granular detergent compositions and a process for producing the granular detergents. More particularly, the present invention relates to granular detergent compositions having an improved solubility.
- GB-A-2 158 087 discloses granular non-caking detergent compositions comprising amine or quaternary ammonium fabric softeners.
- the present invention is directed to a granular detergent composition
- a granular detergent composition comprising from 0.01% to 50% by weight of an anionic sulphonate surfactant, from 0.01% to 45% by weight of a hydrotrope and from 0.5% to 5% by weight of a cationic surfactant.
- the granular detergent composition is substantially free from an anionic sulphate surfactants, and is coated with a water soluble coating material that is a mixture of an anionic sulphonate surfactant and a hydrotrope.
- the granular detergent according to the present invention can provide an improved solubility even in cold water with little of no reduction in cleaning performance.
- An anionic sulphonate surfactant is an essential ingredient for the granular detergent of the present invention.
- a preferable anionic sulphonate surfactant includes the salts (or optionally the acids) of C5-C20 linear or branched alkyl benzene sulphonates, alkyl ester sulphonates, C6-22 primary or secondary alkane sulphonates, C6-C24 olefin sulphonates, sulphonated polycarboxylic acids, alkyl glycerol sulphonates, preferably derived from alcohols derived from tallow or coconut oil, fatty acid glycerol sulphonates, fatty oleyl glycerol sulphonates, and mixtures thereof.
- the cation of the anionic sulphonate surfactant may be any appropriate cations such as sodium, potassium, hydrogen, ammonium or alcohol amine, preferably, sodium or potassium.
- the anionic sulphonate surfactant of the present invention is selected from the group consisting of a sodium or potassium salt of C11-13 branched or linear alkyl benzene sulphonates (LAS), C6-22 primary or secondary paraffine sulphonates (PS), C10-18 methyl ester sulphonates (MES), C6-C24 olefin sulphonates (AOS).
- LAS alkyl benzene sulphonates
- PS C6-22 primary or secondary paraffine sulphonates
- MES C10-18 methyl ester sulphonates
- AOS C6-C24 olefin sulphonates
- the level of the anionic sulphonate surfactants in the granular detergent composition of the present invention is from 0.01% to 50%, preferably, from 20% to 50%, more preferably, from 20% to 45% by weight of the granular detergent.
- the granular detergent composition of the present invention is substantially free of anionic sulphate surfactants.
- substantially free of anionic sulphate surfactants in the present invention means the level of the anionic sulphate surfactants is less than 0.001%, preferably, less than 0.0001%, more preferably, 0%.
- a hydrotrope is an essential ingredient of the granular detergent composition of the present invention.
- Detergent granules containing linear alkyl benzene sulphonate as surfactant tend to gel in contact with water and the sticky gel around the granules makes the granules stick to each other and form clumps.
- the hydrotropes modify the phase behavior of the sulphonate surfactant to a less sticky and less viscous phase and solubilize the sulphonate surfactant more quickly and consequently substantially avoid the formation of clumps or residues during the washing process.
- the hydrotropes of the present invention include sulphonic acid, sulphonate salts, polyethylene glycols, polypropylene glycols and mixtures thereof.
- the preferable ionized-salts are the alkali metal, alkaline earthmetal, alkyl amine and ammonium salts of the sulphonic acid. More preferable salts are selected from the group consisting of sodium, potassium, monoethanolamine sulphonate and mixtures thereof.
- the hydrotrope is selected from the group consisting of the sulphonic acids and sulphonates of lower chain aromatic hydrocarbons, polyethylene glycols, polypropylene glycols and mixtures thereof.
- Preferable sulphonate salts for the hydrotrope of the present invention are, sodium xylene sulphonates, sodium toluene sulphonates, sodium cumene sulphonates, alkyldiphenyloxide disulphonate having an alkyl group chain length of from C1 to C10, and mixtures thereof.
- the level of the hydrotrope in the granular detergent composition of the present invention is from 0.01% to 45%, preferably, from 0.1% to 15%, more preferably, from 0.2% to 10% by weight of the granular detergent composition.
- Cationic surfactants are an essential ingredient of the granular detergent composition of the present invention. It is believed that cationic surfactants have two benefits for obtaining improved cleaning performance of the granular detergent product: surfactant penetration on soils and hardness tolerance. Anionic sulphonate surfactants have negative charges, while soils are generally positive-charged. As a result, the anionic sulphonate surfactants do not penetrate soils as well as positively charged cationic surfactants. Also, in the washing process, anionic sulphonate surfactants tend to precipitate by forming complexes with hardness ions in water such as calcium and magnesium. Thus, the cleaning performance of the granular detergent compositions are reduced.
- cationic surfactants in combination with anionic sulphonate surfactants tend to form micelles. As the micelles do not interact with the hardness ions, the anionic sulphonate surfactants do not precipitate. Thus, the cleaning performance of the granular detergent compositions are not reduced.
- Preferable cationic surfactants are quaternary ammonium surfactants.
- Preferable quaternary ammonium surfactants are selected from the group consisting of mono C6-C16, preferably C6-C10 N-alkyl or alkenyl ammonium surfactants, wherein the remaining N positions are substituted by methyl, hydroxyethyl or hydroxypropyl groups.
- Another preferred cationic surfactant is an C6-C18 alkyl or alkenyl ester of an quaternary ammonium alcohol, such as quaternary choline esters.
- the cationic surfactants have the formula: wherein R1 is C8-C18 hydrocarbyl and mixtures thereof, preferably, C8-14 alkyl, more preferably, C8, C10 or C12 alkyl, and X is an anion, preferably, chloride or bromide.
- the level of the cationic surfactant is from 0.5% to 5%, preferably, from 1 % to 5%, by weight of the granular detergent composition.
- the granular detergent composition of the present invention is made by a process comprising the step of: (a) mixing the anionic sulphonate surfactant, the hydrotrope and the cationic surfactant; (b) adding other detergent ingredients; (c) drying the detergent mixture from step (b); (d) passing the detergent granules to a coating mixer; (e) providing the water soluble coating material to the coating mixer; and (f) at least partially coating the granules in the coating mixer to from the coated detergent granular composition.
- Step (a) is to mix the anionic sulphonate surfactant, hydrotrope and the cationic surfactant, adding water, if necessary.
- the hydrotrope is added to modify the phase structure of the sulphonate surfactant.
- the anionic sulphonate surfactant is mixed with the cationic surfactant, then the hydrotrope is added because the anionic sulphonate surfactant and the cationic surfactant can form an ion pair complex.
- the detergent granules preferably contain the anionic sulphonate surfactant and the hydrotrope, in the ratio of the anionic sulphonate surfactant to the hydrotrope from 50:1 to 1:1, preferably, from 25:1 to 5:1.
- step (b) other detergent ingredients including builders such as carbonates, silicates, zeolites or brighteners are added.
- builders such as carbonates, silicates, zeolites or brighteners
- Step (c) preferably includes spray drying of the mixture obtained from steps (a) and (b) to make granules.
- These granules can be compacted in roll compactors and ground in order to increase the density.
- Spraying dry can be carried out in conventional spray drying equipment such as a conventional tower as well as other spray drying apparatus.
- Conventional spray drying equipment may include, for example, a spray-dryer which is provided by Ohkawara. Co., Ltd. (Japan) or Niro Co., Ltd. (Denmark).
- Conventional spray drying equipment usually has a height of 0.5m to 30m and an inside temperature of from 200°C to 500°C. Examples of the spray-drying process of the present invention are described in U. S. Patent 5,149,455, Jacobs et al, issued September 22, 1992 , and U. S. Patent 5,565,442, Del Greco et al, issued October 15, 1996 .
- the paste of the mixture comprising the anionic sulphonate surfactants, the cationic surfactant and the hydrotrope from step (a) can be agglomerated before step (c).
- the paste from step (a) is fed into a mixer or densifier (such as Lodige Recycler CB30 and Lodige Recycler KM 300 "Ploughshare") for agglomeration.
- a mixer or densifier such as Lodige Recycler CB30 and Lodige Recycler KM 300 "Ploughshare
- the granular detergent compositions of the present invention are coated with a water soluble coating material which is a mixture of an anionic sulphonate surfactant and a hydrotrope.
- Tne granular detergent compositions of the present invention are coated with the water soluble coating material by the following process: (d) passing the detergent granules to a coating mixer; (e) providing the water soluble coating material to the coating mixer; (f) and at least partially coating the granules in the coating mixer to form the coated granular detergent composition.
- Step (d) is to pass the detergent granules from step (c) of the present invention to a coating mixer such as a high or moderate speed mixer after which an optional low or moderate speed.
- a coating mixer such as a high or moderate speed mixer after which an optional low or moderate speed.
- the coating may be carried out in a single mixer that can be low, moderate or high speed.
- the particular mixer used in the present process should include pulverizing or grinding and agglomeration tools so that both techniques can be carried forth simultaneously in a single mixer.
- Residence times of the mixers will vary depending on the type of mixer and the operating parameters.
- the mean residence time is from 0.1 to 60 seconds, more preferably from 0.1 to 30 seconds, even more preferably 0.1 to 15 seconds.
- Other preferred conditions of the high-speed mixer include from 3 to 90 m/s of tip speed, and more preferably from 10 to 70 m/s of tip speed, and from 0.005 W/kg to 100 W/kg of power draw, more preferably from 0.05 W/kg to 80 W/kg of power draw.
- choppers can be used inside the mixer to break up undesirable oversized particles at an rpm of from 0 to 5000 rpm, more preferably from 100 to 3000 rpm.
- the wall temperature is from ambient to 80°C and the spacing between the mixer elements and the wall is from 0.1 cm to 25 cm.
- Examples of a high-speed mixer having a mean residence time of from 0.1 to 60 seconds are Lodige Recycler CB 30TM, by Lodige Company, or mixers made by Drais, Schugi, or a similar brand mixer.
- the mean residence time is from 30 to 1800 seconds, more preferably from 30 to 1200 seconds, more preferably from 30 to 600 seconds.
- Other preferred conditions of the moderate-speed mixer include from 0.1 to 30 m/s of tip speed, and more preferably from 1 to 25 m/s of tip speed, and from 5 W/kg to 1000 W/kg of power draw, more preferably from 20 W/kg to 500 W/kg of power draw.
- choppers can be used inside the mixer to break up undesirable oversized particles at an rpm of from 0 to 5000 rpm, more preferably from 100 to 4000 rpm.
- the wall temperature is from -20°C to 80°C and the spacing between the mixer elements and the wall is from 0.1 cm to 25 cm.
- a moderate-speed mixer having a mean residence time of from 30 to 1800 seconds are Lodige Recycler KM "Ploughshare" 300TM and 600TM, by Lodige Company, the Drais K-T 160TM mixer, or mixers made by Fukae.
- the Lodige KM "Ploughshare" 600TM moderate-speed mixer is a particularly preferred mixer, which comprises a horizontal, hollow static cylinder having a centrally mounted rotating shaft around which several plough-shaped blades are attached.
- the shaft rotates at a speed of from 15 rpm to 140 rpm, more preferably from 80 rpm to 120 rpm.
- the grinding or pulverizing is accomplished by cutters, generally smaller in size that the rotating shaft, which preferably operate at about 3600 rpm.
- the mean residence time is from 30 seconds to 1800 seconds, more preferably from 30 seconds to 1200 seconds, and even more preferably from 30 seconds to 600 seconds.
- the tip speed is preferably from 0.1 m/s to 10 m/s, more preferably from 0.2 m/s to 7 m/s, and even more preferably from 0.2 m/s to 3.5 m/s.
- preferred low-speed mixers include rotating bowl agglomerators, drum agglomerators, pan agglomerators, fluid bed granulators, and extruders.
- An example of an extruder is a multiple-screw extruder by Werner Pfleiderer (Germany).
- the step (c) can be successfully completed, under the process parameters described, in a Lodige KMTM (Ploughshare) moderate speed mixer, Lodige CBTM high speed mixer, or mixers made by Fukae, Drais, Schugi or similar brand mixer.
- the Lodige KMTM (Ploughshare) moderate speed mixer which is a preferred mixer for use in the present invention, comprises a horizontal, hollow static cylinder having a centrally mounted rotating shaft around which several plough-shaped blades are attached.
- Other mixers similar in nature which are suitable for use in the process include the Lodige Ploughshare TM mixer and the Drais® K-T 160 mixer.
- Step (e) is to provide the water soluble coating material to the coating mixer.
- the water soluble coating material is a mixture of an anionic sulphonate surfactant and a hydrotrope.
- anionic sulphonate surfactants and hydrotropes are added in step (a). But additional anionic sulphonate surfactants and hydrotropes are added during this step as well.
- the water soluble coating material is a mixture of the anionic sulphonate surfactant and the hydrotrope in a ratio of the anionic sulphonate to the hydrotrope of from 95:5 to 5:95, more preferably, from 50:1 to 1:1.
- Step (f) is at least partially to coat the granules from step (e) and to obtain the granular detergent compositions of the present invention.
- the granular detergent compositions of the present invention preferably comprise at least 50% by weight of granules having a geometric mean particle diameter of from 400 microns to 1500 microns and preferably have a geometric standard deviation of from 1 to 2.
- the geometric standard deviation is from 1.0 to 1.7, preferably from 1.0 to 1.4.
- the granular detergent composition resulting from the processes may comprise undersized or fine particles, wherein "fine particles" are defined as particles that have a geometric mean particle diameter that is less than 1.65 standard deviations below the chosen geometric mean particle diameter of the granular detergent composition at a given geometric standard deviation.
- Oversized or large particles may also exist wherein "large particles" are defined as particles that have a geometric mean particle diameter that is greater than 1.65 standard deviations above the chosen geometric mean particle diameter of the granular detergent composition at a given geometric standard deviation.
- the fine particles are preferably separated from the granular detergent composition and returned to the process by adding them to at least one of the mixers and/or the fluid bed dryer as described in detail below.
- the large particles are preferably separated from the granular detergent composition and then fed to a grinder where their geometric mean particle diameter is reduced. After the geometric mean particle diameter of the large particles is reduced, the large particles are returned to the process by adding them to at least one of the mixers and/or the fluid bed dryer.
- the granular detergent composition of the present invention can further contain a wide variety of ingredients, including but not limited to optical brighteners, pigments or dyes, chelants, nonionic surfactants, pH control agents, detergency co-builders, fillers and mixtures of these materials.
- Particularly preferred are pigments or dyes such as titanium dioxide, bluing agents such as copper sulfate, zinc thiosulfate and Ultramarine blue, Sparkle enhancers such as mica flake, fillers such as sodium carbonate and sodium sulfate and co-builders such as citrates and nonionic surfactants.
- the granular detergent composition can also contain bleaching agents, bleach activators, enzymes, perfumes, non-coated detergent particles, and various other ingredients to produce a fully formulated detergent composition.
- bleaching agents bleach activators, enzymes, perfumes, non-coated detergent particles, and various other ingredients to produce a fully formulated detergent composition.
- Examples 1, 2 and 3 are comparative examples.
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Abstract
Description
- The present invention relates to granular detergent compositions and a process for producing the granular detergents. More particularly, the present invention relates to granular detergent compositions having an improved solubility.
- Recently, there has been considerable interest within the detergent industry for laundry detergents which have the convenience, aesthetics and solubility of liquid laundry detergent products, but retain the cleaning performance and low cost of granular detergent products. There are some problems associated with past granular detergent compositions with regard to aesthetics, solubility and user convenience. Such problems have been exacerbated by the advent of "compact" or low dosage granular detergent products which typically do not dissolve in washing solutions as well as their liquid laundry detergent counterparts. These low dosage detergents are currently in high demand as they conserve resources and can be sold in small packages which are more convenient for consumers to purchase. But granular detergents are less convenient upon dispensing into the washing machine as compared to liquid laundry detergent which can be simply poured directly from the bottle as opposed to "scooped" from the box and then dispensed into the washing solution.
- As mentioned, such low dosage or "compact" detergent products sometimes experience dissolution problems, especially in cold temperature laundering solutions (i.e., less than about 30°C). More specifically, poor dissolution results in the formation of "clumps" which appear as solid white masses remaining in the washing machine or on the laundered clothes after conventional washing cycles. These "clumps" are especially prevalent under cold temperature washing conditions and when the order of addition to the washing machine is laundry detergent first, clothes second and water last (commonly known as the "Reverse Order Of Addition" or "ROOA"). Such undesirable "clumps" are also formed if the consumer loads the washing machine in the order of clothes, detergent and then water. This clumping phenomenon can contribute to the incomplete dispensing of detergent in washing machines equipped with dispenser drawers or in other dispensing devices, such as a granulette. In this case, the undesired result is undissolved detergent residue in the dispensing device.
- The cause of the aforementioned dissolution problem is generally associated with the "bridging" of a "gel-like" substance between surfactant-containing particles to form undesirable "clumps". However, surfactants are one of the most important ingredients in detergent compositions from cleaning performance standpoint. If reducing the level of surfactants, it may avoid the dissolution problem, but affect the cleaning performance of the product.
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discloses granular non-caking detergent compositions comprising amine or quaternary ammonium fabric softeners.GB-A-2 158 087 - Accordingly, the need remains for a granular detergent having an improved solubility with little or no reduction in cleaning performance.
- The present invention is directed to a granular detergent composition comprising from 0.01% to 50% by weight of an anionic sulphonate surfactant, from 0.01% to 45% by weight of a hydrotrope and from 0.5% to 5% by weight of a cationic surfactant. The granular detergent composition is substantially free from an anionic sulphate surfactants, and is coated with a water soluble coating material that is a mixture of an anionic sulphonate surfactant and a hydrotrope.
- The granular detergent according to the present invention can provide an improved solubility even in cold water with little of no reduction in cleaning performance.
- These and other features, aspects, and advantages of the present invention will become evident to those skilled in the art from a reading of the present disclosure with the appended claims.
- The following is a list of definitions for terms used herein.
- "Comprising" means that other steps and other ingredients which do not affect the end result can be added. This term encompasses the terms "consisting of" and "consisting essentially of".
All percentages are by weight of total composition unless specifically stated otherwise.
The present invention, in its product aspects, is described in detail as follows. - An anionic sulphonate surfactant is an essential ingredient for the granular detergent of the present invention. A preferable anionic sulphonate surfactant includes the salts (or optionally the acids) of C5-C20 linear or branched alkyl benzene sulphonates, alkyl ester sulphonates, C6-22 primary or secondary alkane sulphonates, C6-C24 olefin sulphonates, sulphonated polycarboxylic acids, alkyl glycerol sulphonates, preferably derived from alcohols derived from tallow or coconut oil, fatty acid glycerol sulphonates, fatty oleyl glycerol sulphonates, and mixtures thereof.
- The cation of the anionic sulphonate surfactant may be any appropriate cations such as sodium, potassium, hydrogen, ammonium or alcohol amine, preferably, sodium or potassium.
- More preferably, the anionic sulphonate surfactant of the present invention is selected from the group consisting of a sodium or potassium salt of C11-13 branched or linear alkyl benzene sulphonates (LAS), C6-22 primary or secondary paraffine sulphonates (PS), C10-18 methyl ester sulphonates (MES), C6-C24 olefin sulphonates (AOS).
- The level of the anionic sulphonate surfactants in the granular detergent composition of the present invention is from 0.01% to 50%, preferably, from 20% to 50%, more preferably, from 20% to 45% by weight of the granular detergent.
- The granular detergent composition of the present invention is substantially free of anionic sulphate surfactants. "substantially free of anionic sulphate surfactants" in the present invention means the level of the anionic sulphate surfactants is less than 0.001%, preferably, less than 0.0001%, more preferably, 0%.
- A hydrotrope is an essential ingredient of the granular detergent composition of the present invention. Detergent granules containing linear alkyl benzene sulphonate as surfactant tend to gel in contact with water and the sticky gel around the granules makes the granules stick to each other and form clumps. Not wanting to be limited by theory, it is believed that the hydrotropes modify the phase behavior of the sulphonate surfactant to a less sticky and less viscous phase and solubilize the sulphonate surfactant more quickly and consequently substantially avoid the formation of clumps or residues during the washing process.
- Other suitable hydrotropes for use are described in known texts such as Mitijevic, "Surface and Colloid Science" Plenum Press, vol 15(1993).
- Preferably, the hydrotropes of the present invention include sulphonic acid, sulphonate salts, polyethylene glycols, polypropylene glycols and mixtures thereof.
- The preferable ionized-salts are the alkali metal, alkaline earthmetal, alkyl amine and ammonium salts of the sulphonic acid. More preferable salts are selected from the group consisting of sodium, potassium, monoethanolamine sulphonate and mixtures thereof.
- More preferably, the hydrotrope is selected from the group consisting of the sulphonic acids and sulphonates of lower chain aromatic hydrocarbons, polyethylene glycols, polypropylene glycols and mixtures thereof.
- Preferable sulphonate salts for the hydrotrope of the present invention are, sodium xylene sulphonates, sodium toluene sulphonates, sodium cumene sulphonates, alkyldiphenyloxide disulphonate having an alkyl group chain length of from C1 to C10, and mixtures thereof.
- The level of the hydrotrope in the granular detergent composition of the present invention is from 0.01% to 45%, preferably, from 0.1% to 15%, more preferably, from 0.2% to 10% by weight of the granular detergent composition.
- Cationic surfactants are an essential ingredient of the granular detergent composition of the present invention. It is believed that cationic surfactants have two benefits for obtaining improved cleaning performance of the granular detergent product: surfactant penetration on soils and hardness tolerance. Anionic sulphonate surfactants have negative charges, while soils are generally positive-charged. As a result, the anionic sulphonate surfactants do not penetrate soils as well as positively charged cationic surfactants. Also, in the washing process, anionic sulphonate surfactants tend to precipitate by forming complexes with hardness ions in water such as calcium and magnesium. Thus, the cleaning performance of the granular detergent compositions are reduced. But, cationic surfactants in combination with anionic sulphonate surfactants, tend to form micelles. As the micelles do not interact with the hardness ions, the anionic sulphonate surfactants do not precipitate. Thus, the cleaning performance of the granular detergent compositions are not reduced.
- Preferable cationic surfactants are quaternary ammonium surfactants. Preferable quaternary ammonium surfactants are selected from the group consisting of mono C6-C16, preferably C6-C10 N-alkyl or alkenyl ammonium surfactants, wherein the remaining N positions are substituted by methyl, hydroxyethyl or hydroxypropyl groups. Another preferred cationic surfactant is an C6-C18 alkyl or alkenyl ester of an quaternary ammonium alcohol, such as quaternary choline esters.
-
- The level of the cationic surfactant is from 0.5% to 5%, preferably, from 1 % to 5%, by weight of the granular detergent composition.
- The granular detergent composition of the present invention is made by a process comprising the step of: (a) mixing the anionic sulphonate surfactant, the hydrotrope and the cationic surfactant; (b) adding other detergent ingredients; (c) drying the detergent mixture from step (b); (d) passing the detergent granules to a coating mixer; (e) providing the water soluble coating material to the coating mixer; and (f) at least partially coating the granules in the coating mixer to from the coated detergent granular composition.
- Step (a) is to mix the anionic sulphonate surfactant, hydrotrope and the cationic surfactant, adding water, if necessary. The hydrotrope is added to modify the phase structure of the sulphonate surfactant. Preferably, the anionic sulphonate surfactant is mixed with the cationic surfactant, then the hydrotrope is added because the anionic sulphonate surfactant and the cationic surfactant can form an ion pair complex. The detergent granules preferably contain the anionic sulphonate surfactant and the hydrotrope, in the ratio of the anionic sulphonate surfactant to the hydrotrope from 50:1 to 1:1, preferably, from 25:1 to 5:1.
- In step (b), other detergent ingredients including builders such as carbonates, silicates, zeolites or brighteners are added.
- Step (c) preferably includes spray drying of the mixture obtained from steps (a) and (b) to make granules. These granules can be compacted in roll compactors and ground in order to increase the density. Spraying dry can be carried out in conventional spray drying equipment such as a conventional tower as well as other spray drying apparatus. Conventional spray drying equipment may include, for example, a spray-dryer which is provided by Ohkawara. Co., Ltd. (Japan) or Niro Co., Ltd. (Denmark). For drying detergent granules conventional spray drying equipment usually has a height of 0.5m to 30m and an inside temperature of from 200°C to 500°C. Examples of the spray-drying process of the present invention are described in U. S. Patent
5,149,455, Jacobs et al, issued September 22, 1992 , and U. S. Patent5,565,442, Del Greco et al, issued October 15, 1996 . - The paste of the mixture comprising the anionic sulphonate surfactants, the cationic surfactant and the hydrotrope from step (a) can be agglomerated before step (c). In such agglomeration process, the paste from step (a) is fed into a mixer or densifier (such as Lodige Recycler CB30 and Lodige Recycler KM 300 "Ploughshare") for agglomeration. Preferable agglomeration processes are disclosed in U. S. Patent No.
5,366,652, Scott et al, issued November 22, 1994 and U. S. Patent, Lisa et al, issued April 28, 1992. - The granular detergent compositions of the present invention are coated with a water soluble coating material which is a mixture of an anionic sulphonate surfactant and a hydrotrope. Tne granular detergent compositions of the present invention are coated with the water soluble coating material by the following process: (d) passing the detergent granules to a coating mixer; (e) providing the water soluble coating material to the coating mixer; (f) and at least partially coating the granules in the coating mixer to form the coated granular detergent composition.
- Step (d) is to pass the detergent granules from step (c) of the present invention to a coating mixer such as a high or moderate speed mixer after which an optional low or moderate speed. Alternatively, the coating may be carried out in a single mixer that can be low, moderate or high speed. The particular mixer used in the present process should include pulverizing or grinding and agglomeration tools so that both techniques can be carried forth simultaneously in a single mixer.
- Residence times of the mixers will vary depending on the type of mixer and the operating parameters. For a preferred high-speed mixer, the mean residence time is from 0.1 to 60 seconds, more preferably from 0.1 to 30 seconds, even more preferably 0.1 to 15 seconds. Other preferred conditions of the high-speed mixer include from 3 to 90 m/s of tip speed, and more preferably from 10 to 70 m/s of tip speed, and from 0.005 W/kg to 100 W/kg of power draw, more preferably from 0.05 W/kg to 80 W/kg of power draw. Preferably, if choppers are used, choppers can be used inside the mixer to break up undesirable oversized particles at an rpm of from 0 to 5000 rpm, more preferably from 100 to 3000 rpm. Preferably, the wall temperature is from ambient to 80°C and the spacing between the mixer elements and the wall is from 0.1 cm to 25 cm. Examples of a high-speed mixer having a mean residence time of from 0.1 to 60 seconds are Lodige Recycler CB 30™, by Lodige Company, or mixers made by Drais, Schugi, or a similar brand mixer.
- For a preferred moderate-speed mixer, the mean residence time is from 30 to 1800 seconds, more preferably from 30 to 1200 seconds, more preferably from 30 to 600 seconds. Other preferred conditions of the moderate-speed mixer include from 0.1 to 30 m/s of tip speed, and more preferably from 1 to 25 m/s of tip speed, and from 5 W/kg to 1000 W/kg of power draw, more preferably from 20 W/kg to 500 W/kg of power draw. Preferably, if choppers are used, choppers can be used inside the mixer to break up undesirable oversized particles at an rpm of from 0 to 5000 rpm, more preferably from 100 to 4000 rpm. Preferably, the wall temperature is from -20°C to 80°C and the spacing between the mixer elements and the wall is from 0.1 cm to 25 cm. Examples of a moderate-speed mixer having a mean residence time of from 30 to 1800 seconds are Lodige Recycler KM "Ploughshare" 300™ and 600™, by Lodige Company, the Drais K-T 160™ mixer, or mixers made by Fukae. The Lodige KM "Ploughshare" 600™ moderate-speed mixer is a particularly preferred mixer, which comprises a horizontal, hollow static cylinder having a centrally mounted rotating shaft around which several plough-shaped blades are attached. Preferably, the shaft rotates at a speed of from 15 rpm to 140 rpm, more preferably from 80 rpm to 120 rpm. In a preferred mixer, the grinding or pulverizing is accomplished by cutters, generally smaller in size that the rotating shaft, which preferably operate at about 3600 rpm.
- For a preferred low-speed mixer, the mean residence time is from 30 seconds to 1800 seconds, more preferably from 30 seconds to 1200 seconds, and even more preferably from 30 seconds to 600 seconds. The tip speed is preferably from 0.1 m/s to 10 m/s, more preferably from 0.2 m/s to 7 m/s, and even more preferably from 0.2 m/s to 3.5 m/s. Examples of preferred low-speed mixers include rotating bowl agglomerators, drum agglomerators, pan agglomerators, fluid bed granulators, and extruders. An example of an extruder is a multiple-screw extruder by Werner Pfleiderer (Germany).
- In one preferred embodiment it has been found that the step (c) can be successfully completed, under the process parameters described, in a Lodige KM™ (Ploughshare) moderate speed mixer, Lodige CB™ high speed mixer, or mixers made by Fukae, Drais, Schugi or similar brand mixer. The Lodige KM™ (Ploughshare) moderate speed mixer, which is a preferred mixer for use in the present invention, comprises a horizontal, hollow static cylinder having a centrally mounted rotating shaft around which several plough-shaped blades are attached. Other mixers similar in nature which are suitable for use in the process include the Lodige Ploughshare™ mixer and the Drais® K-T 160 mixer. Step (e) is to provide the water soluble coating material to the coating mixer. The water soluble coating material is a mixture of an anionic sulphonate surfactant and a hydrotrope. As explained, anionic sulphonate surfactants and hydrotropes are added in step (a). But additional anionic sulphonate surfactants and hydrotropes are added during this step as well. Preferably, the water soluble coating material is a mixture of the anionic sulphonate surfactant and the hydrotrope in a ratio of the anionic sulphonate to the hydrotrope of from 95:5 to 5:95, more preferably, from 50:1 to 1:1.
- Step (f) is at least partially to coat the granules from step (e) and to obtain the granular detergent compositions of the present invention.
- The granular detergent compositions of the present invention preferably comprise at least 50% by weight of granules having a geometric mean particle diameter of from 400 microns to 1500 microns and preferably have a geometric standard deviation of from 1 to 2. Preferably the geometric standard deviation is from 1.0 to 1.7, preferably from 1.0 to 1.4. The granular detergent composition resulting from the processes may comprise undersized or fine particles, wherein "fine particles" are defined as particles that have a geometric mean particle diameter that is less than 1.65 standard deviations below the chosen geometric mean particle diameter of the granular detergent composition at a given geometric standard deviation. Oversized or large particles may also exist wherein "large particles" are defined as particles that have a geometric mean particle diameter that is greater than 1.65 standard deviations above the chosen geometric mean particle diameter of the granular detergent composition at a given geometric standard deviation. The fine particles are preferably separated from the granular detergent composition and returned to the process by adding them to at least one of the mixers and/or the fluid bed dryer as described in detail below. Likewise, the large particles are preferably separated from the granular detergent composition and then fed to a grinder where their geometric mean particle diameter is reduced. After the geometric mean particle diameter of the large particles is reduced, the large particles are returned to the process by adding them to at least one of the mixers and/or the fluid bed dryer.
- The granular detergent composition of the present invention can further contain a wide variety of ingredients, including but not limited to optical brighteners, pigments or dyes, chelants, nonionic surfactants, pH control agents, detergency co-builders, fillers and mixtures of these materials. Particularly preferred are pigments or dyes such as titanium dioxide, bluing agents such as copper sulfate, zinc thiosulfate and Ultramarine blue, Sparkle enhancers such as mica flake, fillers such as sodium carbonate and sodium sulfate and co-builders such as citrates and nonionic surfactants.
- The granular detergent composition can also contain bleaching agents, bleach activators, enzymes, perfumes, non-coated detergent particles, and various other ingredients to produce a fully formulated detergent composition.
These suitable ingredients are disclosed and exemplified in U. S. Patent No.5,756,444, issued May 26, 1998 to Scott et al , in U. S. Patent No.5,478,503, issued Dec. 26, 1995 to Ronald . - The aspects and embodiments of the invention set forth in this document have many advantages, including an improved solubility with little or no reduction in cleaning performance.
- The following examples further describe and demonstrate the preferred embodiments within the scope of the present invention. The examples are given solely for the purpose of illustration.
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weight % 1 2 3 4 5 6 7 8 LAS* 30 30 30 20 25 25 25 25 SXS** 4 2 1 4 2 1 3 3 Polyethylene glycol 0.1 - 0.1 0.1 0.5 0.1 0.5 0.5 CocoK3 2 2 2 2 2 1 1 1 Brighteners 0.35 0.35 0.35 0.35 0.35 0.35 0.35 0.35 Sodium carbonate 20 20 20 20 30 20 30 30 Zeolite A 5 5 5 10 5 5 10 10 Acrylic-Maleic acid 10 10 10 10 10 10 10 10 copolymer Silicate 15 15 15 15 0 15 0 0 Coating material LAS - 6 - 6 6 6 6 6 SXS - - 3 2 1 0.5 0.5 - Polyethylene glycol - - - - - - - 3 Sodium percarbonate 3.2 3.2 3.2 3.2 3.2 3.2 3.2 3.2 NOBS*** 2.7 2.7 2.7 2.7 2.7 2.7 2.7 2.7 Perfume 0.2 0.2 0.2 0.2 0.2 0.2 0.2 0.2 Protease 0.5 0.5 0.5 0.5 0.5 0.5 0.5 0.5 Minors up to 100% *40% Linear Alkylbenzene Sulphonate paste
** 20% Sodium Xylene Sulphonate solution
*** Sodium nonanoyloxybenzene Sulphonate (bleach activator) - Examples 1, 2 and 3 are comparative examples.
Claims (7)
- A granular detergent composition comprising:(a) from 0.01% to 50% by weight of an anionic sulphonate surfactant;(b) from 0.01% to 45% by weight of a hydrotrope; and(c) from 0.5% to 5% by weight of a cationic surfactant,wherein the granular detergent composition is substantially free of anionic sulphate surfactants, wherein the detergent composition is coated with a water soluble coating material that is a mixture of an anionic sulphonate surfactant and a hydrotrope.
- The granular detergent composition according to Claim 1, wherein the detergent composition comprises from 20% to 50% by weight of an anionic sulphonate surfactant.
- The granular detergent composition according to Claim 1, wherein the water soluble coating material comprises a hydrotrope selected from the group consisting of polyethylene glycols, polypropylene glycols, sulphonate salts and mixtures thereof.
- The granular detergent composition according to Claim 1, wherein the hydrotrope is selected from the group consisting of sodium xylene sulphonate, sodium toluene sulphonate, sodium cumene sulphonate , alkyldiphenyloxide disulphonate having an alkyl group chain length of from C1 to C10, and mixtures thereof
- The granular detergent composition according to Claim 1, wherein the water soluble coating material is a mixture of an anionic sulphonate surfactant and a hydrotrope in a ratio of anionic sulphonate surfactant to hydrotrope of from 95:5 to 5:95.
- The granular detergent composition according to Claim 1, wherein the detergent composition has a geometric mean particle diameter of from 400 microns to 1500 microns with a geometric standard deviation of from 1 to 2.
- A process for preparing the granular detergent composition according to Claim 1, comprising the steps of:(a) mixing the anionic sulphonate surfactant, the hydrotrope and the cationic surfactant;(b) adding other detergent ingredients;(c) drying the detergent mixture from step (b);(d) passing the detergent granules to a coating mixer;(e) providing the water soluble coating material to the coating mixer; and(f) at least partially coating the granules in the coating mixer to form the coated detergent granular composition.
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| PCT/US2000/019136 WO2002006432A1 (en) | 2000-07-13 | 2000-07-13 | Granular detergent composition having an improved solubility |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| EP1299511A1 EP1299511A1 (en) | 2003-04-09 |
| EP1299511B1 true EP1299511B1 (en) | 2008-05-14 |
Family
ID=21741589
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| EP00948658A Expired - Lifetime EP1299511B1 (en) | 2000-07-13 | 2000-07-13 | Granular detergent composition having an improved solubility |
Country Status (10)
| Country | Link |
|---|---|
| EP (1) | EP1299511B1 (en) |
| JP (1) | JP2004504444A (en) |
| CN (1) | CN1268728C (en) |
| AT (1) | ATE395402T1 (en) |
| AU (1) | AU2000262128A1 (en) |
| BR (1) | BR0017259A (en) |
| CA (1) | CA2413199A1 (en) |
| DE (1) | DE60038905D1 (en) |
| MX (1) | MXPA03000332A (en) |
| WO (1) | WO2002006432A1 (en) |
Families Citing this family (4)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JP5424527B2 (en) * | 2006-09-29 | 2014-02-26 | 小林製薬株式会社 | Solid cleaning agent for flush toilet |
| CN102277238B (en) * | 2011-07-13 | 2012-10-03 | 杭州迪康生物技术有限公司 | Granular fatty acid methyl ester sulfonate (MES)-containing composite |
| CN103881844B (en) * | 2012-12-20 | 2017-03-08 | 广州市浪奇实业股份有限公司 | Granulated detergent compositionss and preparation method thereof |
| CN111315858B (en) * | 2017-11-14 | 2021-12-24 | 宝洁公司 | Particulate antimicrobial laundry detergent composition |
Family Cites Families (5)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| BE757913A (en) * | 1969-10-24 | 1971-04-01 | Colgate Palmolive Co | DETERGENT COMPOSITION IN PARTICLES |
| GB2158087B (en) * | 1984-05-04 | 1987-11-04 | Procter & Gamble | Non-caking detergent composition |
| EP0934378B1 (en) * | 1996-10-18 | 2003-06-11 | The Procter & Gamble Company | Detergent compositions comprising a mixture of cationic, anionic and nonionic surfactants |
| ES2184523T3 (en) * | 1998-10-26 | 2003-04-01 | Procter & Gamble | PROCEDURES FOR OBTAINING A DETERGENT GRANULAR COMPOSITION THAT HAS AN IMPROVED ASPECT AND SOLUBILITY. |
| EP1785479A1 (en) * | 1999-08-10 | 2007-05-16 | The Procter and Gamble Company | Detergent compositions comprising hydrotropes |
-
2000
- 2000-07-13 DE DE60038905T patent/DE60038905D1/en not_active Expired - Fee Related
- 2000-07-13 AT AT00948658T patent/ATE395402T1/en not_active IP Right Cessation
- 2000-07-13 CA CA002413199A patent/CA2413199A1/en not_active Abandoned
- 2000-07-13 WO PCT/US2000/019136 patent/WO2002006432A1/en not_active Ceased
- 2000-07-13 EP EP00948658A patent/EP1299511B1/en not_active Expired - Lifetime
- 2000-07-13 BR BR0017259-6A patent/BR0017259A/en not_active Application Discontinuation
- 2000-07-13 CN CN00819753.9A patent/CN1268728C/en not_active Expired - Fee Related
- 2000-07-13 JP JP2002512326A patent/JP2004504444A/en not_active Withdrawn
- 2000-07-13 MX MXPA03000332A patent/MXPA03000332A/en active IP Right Grant
- 2000-07-13 AU AU2000262128A patent/AU2000262128A1/en not_active Abandoned
Also Published As
| Publication number | Publication date |
|---|---|
| EP1299511A1 (en) | 2003-04-09 |
| ATE395402T1 (en) | 2008-05-15 |
| CN1268728C (en) | 2006-08-09 |
| MXPA03000332A (en) | 2004-05-21 |
| WO2002006432A8 (en) | 2002-05-30 |
| BR0017259A (en) | 2003-06-24 |
| JP2004504444A (en) | 2004-02-12 |
| DE60038905D1 (en) | 2008-06-26 |
| CA2413199A1 (en) | 2002-01-24 |
| WO2002006432A1 (en) | 2002-01-24 |
| AU2000262128A1 (en) | 2002-01-30 |
| CN1471568A (en) | 2004-01-28 |
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