WO2022243343A1 - Process for preparing a spray dried detergent particle - Google Patents
Process for preparing a spray dried detergent particle Download PDFInfo
- Publication number
- WO2022243343A1 WO2022243343A1 PCT/EP2022/063372 EP2022063372W WO2022243343A1 WO 2022243343 A1 WO2022243343 A1 WO 2022243343A1 EP 2022063372 W EP2022063372 W EP 2022063372W WO 2022243343 A1 WO2022243343 A1 WO 2022243343A1
- Authority
- WO
- WIPO (PCT)
- Prior art keywords
- spray
- anionic surfactant
- detergent
- dried
- particle
- Prior art date
Links
- 239000003599 detergent Substances 0.000 title claims abstract description 213
- 239000002245 particle Substances 0.000 title claims abstract description 147
- 238000004519 manufacturing process Methods 0.000 title claims abstract description 27
- 239000007921 spray Substances 0.000 title claims description 39
- 239000000203 mixture Substances 0.000 claims abstract description 68
- 239000002002 slurry Substances 0.000 claims abstract description 67
- 238000000034 method Methods 0.000 claims abstract description 54
- 238000001694 spray drying Methods 0.000 claims abstract description 48
- CDBYLPFSWZWCQE-UHFFFAOYSA-L Sodium Carbonate Chemical compound [Na+].[Na+].[O-]C([O-])=O CDBYLPFSWZWCQE-UHFFFAOYSA-L 0.000 claims abstract description 29
- 229910000029 sodium carbonate Inorganic materials 0.000 claims abstract description 15
- NTHWMYGWWRZVTN-UHFFFAOYSA-N sodium silicate Chemical compound [Na+].[Na+].[O-][Si]([O-])=O NTHWMYGWWRZVTN-UHFFFAOYSA-N 0.000 claims abstract description 13
- 239000004115 Sodium Silicate Substances 0.000 claims abstract description 12
- 229910052911 sodium silicate Inorganic materials 0.000 claims abstract description 12
- 239000003945 anionic surfactant Substances 0.000 claims description 102
- 239000002253 acid Substances 0.000 claims description 92
- 230000003472 neutralizing effect Effects 0.000 claims description 73
- 239000002243 precursor Substances 0.000 claims description 65
- 239000003795 chemical substances by application Substances 0.000 claims description 62
- BPQQTUXANYXVAA-UHFFFAOYSA-N Orthosilicate Chemical compound [O-][Si]([O-])([O-])[O-] BPQQTUXANYXVAA-UHFFFAOYSA-N 0.000 claims description 37
- 150000003839 salts Chemical class 0.000 claims description 35
- 238000006386 neutralization reaction Methods 0.000 claims description 33
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 claims description 32
- 239000004615 ingredient Substances 0.000 claims description 30
- 239000007788 liquid Substances 0.000 claims description 27
- 150000008044 alkali metal hydroxides Chemical class 0.000 claims description 25
- -1 alkaline earth metal salt Chemical class 0.000 claims description 25
- 239000000945 filler Substances 0.000 claims description 23
- 238000011065 in-situ storage Methods 0.000 claims description 22
- 239000004094 surface-active agent Substances 0.000 claims description 19
- PMZURENOXWZQFD-UHFFFAOYSA-L Sodium Sulfate Chemical group [Na+].[Na+].[O-]S([O-])(=O)=O PMZURENOXWZQFD-UHFFFAOYSA-L 0.000 claims description 18
- FAPWRFPIFSIZLT-UHFFFAOYSA-M Sodium chloride Chemical compound [Na+].[Cl-] FAPWRFPIFSIZLT-UHFFFAOYSA-M 0.000 claims description 16
- 150000004996 alkyl benzenes Chemical group 0.000 claims description 16
- 238000002156 mixing Methods 0.000 claims description 15
- 229920000642 polymer Polymers 0.000 claims description 14
- VTYYLEPIZMXCLO-UHFFFAOYSA-L Calcium carbonate Chemical compound [Ca+2].[O-]C([O-])=O VTYYLEPIZMXCLO-UHFFFAOYSA-L 0.000 claims description 12
- 150000004760 silicates Chemical class 0.000 claims description 11
- 229910052784 alkaline earth metal Inorganic materials 0.000 claims description 10
- 229910052938 sodium sulfate Inorganic materials 0.000 claims description 9
- 235000011152 sodium sulphate Nutrition 0.000 claims description 9
- 238000006243 chemical reaction Methods 0.000 claims description 8
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N silicon dioxide Inorganic materials O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 claims description 8
- 239000011780 sodium chloride Substances 0.000 claims description 8
- BVKZGUZCCUSVTD-UHFFFAOYSA-L Carbonate Chemical compound [O-]C([O-])=O BVKZGUZCCUSVTD-UHFFFAOYSA-L 0.000 claims description 7
- 229910052783 alkali metal Inorganic materials 0.000 claims description 7
- 229910052910 alkali metal silicate Inorganic materials 0.000 claims description 7
- 229910021532 Calcite Inorganic materials 0.000 claims description 6
- 150000001340 alkali metals Chemical class 0.000 claims description 6
- 229910000019 calcium carbonate Inorganic materials 0.000 claims description 6
- 229910001514 alkali metal chloride Inorganic materials 0.000 claims description 5
- 229910052936 alkali metal sulfate Inorganic materials 0.000 claims description 5
- ZLNQQNXFFQJAID-UHFFFAOYSA-L magnesium carbonate Chemical compound [Mg+2].[O-]C([O-])=O ZLNQQNXFFQJAID-UHFFFAOYSA-L 0.000 claims description 5
- 239000001095 magnesium carbonate Substances 0.000 claims description 5
- 229910000021 magnesium carbonate Inorganic materials 0.000 claims description 5
- 229910000514 dolomite Inorganic materials 0.000 claims description 4
- 239000010459 dolomite Substances 0.000 claims description 4
- 238000002360 preparation method Methods 0.000 claims description 4
- HHSPVTKDOHQBKF-UHFFFAOYSA-J calcium;magnesium;dicarbonate Chemical compound [Mg+2].[Ca+2].[O-]C([O-])=O.[O-]C([O-])=O HHSPVTKDOHQBKF-UHFFFAOYSA-J 0.000 claims description 3
- 239000012736 aqueous medium Substances 0.000 claims description 2
- 150000007942 carboxylates Chemical class 0.000 claims description 2
- 239000000843 powder Substances 0.000 abstract description 25
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- HEMHJVSKTPXQMS-UHFFFAOYSA-M sodium hydroxide Inorganic materials [OH-].[Na+] HEMHJVSKTPXQMS-UHFFFAOYSA-M 0.000 description 92
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- BDHFUVZGWQCTTF-UHFFFAOYSA-N sulfonic acid Chemical compound OS(=O)=O BDHFUVZGWQCTTF-UHFFFAOYSA-N 0.000 description 8
- NIXOWILDQLNWCW-UHFFFAOYSA-N acrylic acid group Chemical group C(C=C)(=O)O NIXOWILDQLNWCW-UHFFFAOYSA-N 0.000 description 7
- 239000007864 aqueous solution Substances 0.000 description 7
- 239000001117 sulphuric acid Substances 0.000 description 7
- 235000011149 sulphuric acid Nutrition 0.000 description 7
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- CSNNHWWHGAXBCP-UHFFFAOYSA-L Magnesium sulfate Chemical compound [Mg+2].[O-][S+2]([O-])([O-])[O-] CSNNHWWHGAXBCP-UHFFFAOYSA-L 0.000 description 6
- KWYUFKZDYYNOTN-UHFFFAOYSA-M Potassium hydroxide Chemical compound [OH-].[K+] KWYUFKZDYYNOTN-UHFFFAOYSA-M 0.000 description 6
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- 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 5
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- 238000009472 formulation Methods 0.000 description 5
- 229910052816 inorganic phosphate Inorganic materials 0.000 description 5
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- 235000014113 dietary fatty acids Nutrition 0.000 description 4
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- SMZOUWXMTYCWNB-UHFFFAOYSA-N 2-(2-methoxy-5-methylphenyl)ethanamine Chemical compound COC1=CC=C(C)C=C1CCN SMZOUWXMTYCWNB-UHFFFAOYSA-N 0.000 description 3
- YGUMVDWOQQJBGA-VAWYXSNFSA-N 5-[(4-anilino-6-morpholin-4-yl-1,3,5-triazin-2-yl)amino]-2-[(e)-2-[4-[(4-anilino-6-morpholin-4-yl-1,3,5-triazin-2-yl)amino]-2-sulfophenyl]ethenyl]benzenesulfonic acid Chemical compound C=1C=C(\C=C\C=2C(=CC(NC=3N=C(N=C(NC=4C=CC=CC=4)N=3)N3CCOCC3)=CC=2)S(O)(=O)=O)C(S(=O)(=O)O)=CC=1NC(N=C(N=1)N2CCOCC2)=NC=1NC1=CC=CC=C1 YGUMVDWOQQJBGA-VAWYXSNFSA-N 0.000 description 3
- 102100032487 Beta-mannosidase Human genes 0.000 description 3
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- 125000000217 alkyl group Chemical group 0.000 description 3
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- 150000001860 citric acid derivatives Chemical class 0.000 description 3
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- 150000004665 fatty acids Chemical class 0.000 description 3
- 229910052943 magnesium sulfate Inorganic materials 0.000 description 3
- 235000019341 magnesium sulphate Nutrition 0.000 description 3
- VZCYOOQTPOCHFL-UPHRSURJSA-N maleic acid Chemical compound OC(=O)\C=C/C(O)=O VZCYOOQTPOCHFL-UPHRSURJSA-N 0.000 description 3
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- VZCYOOQTPOCHFL-UHFFFAOYSA-N trans-butenedioic acid Natural products OC(=O)C=CC(O)=O VZCYOOQTPOCHFL-UHFFFAOYSA-N 0.000 description 3
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- CFPOJWPDQWJEMO-UHFFFAOYSA-N 2-(1,2-dicarboxyethoxy)butanedioic acid Chemical class OC(=O)CC(C(O)=O)OC(C(O)=O)CC(O)=O CFPOJWPDQWJEMO-UHFFFAOYSA-N 0.000 description 2
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- CNGYZEMWVAWWOB-VAWYXSNFSA-N 5-[[4-anilino-6-[bis(2-hydroxyethyl)amino]-1,3,5-triazin-2-yl]amino]-2-[(e)-2-[4-[[4-anilino-6-[bis(2-hydroxyethyl)amino]-1,3,5-triazin-2-yl]amino]-2-sulfophenyl]ethenyl]benzenesulfonic acid Chemical compound N=1C(NC=2C=C(C(\C=C\C=3C(=CC(NC=4N=C(N=C(NC=5C=CC=CC=5)N=4)N(CCO)CCO)=CC=3)S(O)(=O)=O)=CC=2)S(O)(=O)=O)=NC(N(CCO)CCO)=NC=1NC1=CC=CC=C1 CNGYZEMWVAWWOB-VAWYXSNFSA-N 0.000 description 2
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- 108010059345 keratinase Proteins 0.000 description 1
- 108010062085 ligninase Proteins 0.000 description 1
- PAZHGORSDKKUPI-UHFFFAOYSA-N lithium metasilicate Chemical compound [Li+].[Li+].[O-][Si]([O-])=O PAZHGORSDKKUPI-UHFFFAOYSA-N 0.000 description 1
- 229910052912 lithium silicate Inorganic materials 0.000 description 1
- 238000011068 loading method Methods 0.000 description 1
- 229910001425 magnesium ion Inorganic materials 0.000 description 1
- 238000005259 measurement Methods 0.000 description 1
- 150000002736 metal compounds Chemical class 0.000 description 1
- XJRBAMWJDBPFIM-UHFFFAOYSA-N methyl vinyl ether Chemical compound COC=C XJRBAMWJDBPFIM-UHFFFAOYSA-N 0.000 description 1
- 230000007935 neutral effect Effects 0.000 description 1
- MGFYIUFZLHCRTH-UHFFFAOYSA-N nitrilotriacetic acid Chemical compound OC(=O)CN(CC(O)=O)CC(O)=O MGFYIUFZLHCRTH-UHFFFAOYSA-N 0.000 description 1
- JRZJOMJEPLMPRA-UHFFFAOYSA-N olefin Natural products CCCCCCCC=C JRZJOMJEPLMPRA-UHFFFAOYSA-N 0.000 description 1
- 230000003287 optical effect Effects 0.000 description 1
- 239000005416 organic matter Substances 0.000 description 1
- 238000001139 pH measurement Methods 0.000 description 1
- 108010087558 pectate lyase Proteins 0.000 description 1
- 229960003330 pentetic acid Drugs 0.000 description 1
- 239000002304 perfume Substances 0.000 description 1
- 230000000704 physical effect Effects 0.000 description 1
- 239000000049 pigment Substances 0.000 description 1
- 229920000573 polyethylene Polymers 0.000 description 1
- 229920001223 polyethylene glycol Polymers 0.000 description 1
- 239000001205 polyphosphate Substances 0.000 description 1
- 235000011176 polyphosphates Nutrition 0.000 description 1
- 229920001451 polypropylene glycol Polymers 0.000 description 1
- BITYAPCSNKJESK-UHFFFAOYSA-N potassiosodium Chemical compound [Na].[K] BITYAPCSNKJESK-UHFFFAOYSA-N 0.000 description 1
- 229910000027 potassium carbonate Inorganic materials 0.000 description 1
- NNHHDJVEYQHLHG-UHFFFAOYSA-N potassium silicate Chemical compound [K+].[K+].[O-][Si]([O-])=O NNHHDJVEYQHLHG-UHFFFAOYSA-N 0.000 description 1
- 229910052913 potassium silicate Inorganic materials 0.000 description 1
- 230000001376 precipitating effect Effects 0.000 description 1
- 238000001556 precipitation Methods 0.000 description 1
- 238000012545 processing Methods 0.000 description 1
- 230000010349 pulsation Effects 0.000 description 1
- 150000003219 pyrazolines Chemical class 0.000 description 1
- 239000002994 raw material Substances 0.000 description 1
- 239000011541 reaction mixture Substances 0.000 description 1
- 230000015227 regulation of liquid surface tension Effects 0.000 description 1
- 230000035945 sensitivity Effects 0.000 description 1
- 239000003352 sequestering agent Substances 0.000 description 1
- 239000000377 silicon dioxide Substances 0.000 description 1
- 235000012239 silicon dioxide Nutrition 0.000 description 1
- 238000004513 sizing Methods 0.000 description 1
- 229910021647 smectite Inorganic materials 0.000 description 1
- 235000019812 sodium carboxymethyl cellulose Nutrition 0.000 description 1
- 229920001027 sodium carboxymethylcellulose Polymers 0.000 description 1
- 159000000000 sodium salts Chemical class 0.000 description 1
- 235000019832 sodium triphosphate Nutrition 0.000 description 1
- QUCDWLYKDRVKMI-UHFFFAOYSA-M sodium;3,4-dimethylbenzenesulfonate Chemical compound [Na+].CC1=CC=C(S([O-])(=O)=O)C=C1C QUCDWLYKDRVKMI-UHFFFAOYSA-M 0.000 description 1
- 239000013042 solid detergent Substances 0.000 description 1
- 239000008247 solid mixture Substances 0.000 description 1
- 238000005507 spraying Methods 0.000 description 1
- 239000003381 stabilizer Substances 0.000 description 1
- 230000003068 static effect Effects 0.000 description 1
- 239000013589 supplement Substances 0.000 description 1
- 108010038851 tannase Proteins 0.000 description 1
- 238000012360 testing method Methods 0.000 description 1
- 238000004448 titration Methods 0.000 description 1
- 150000003852 triazoles Chemical class 0.000 description 1
- 239000004034 viscosity adjusting agent Substances 0.000 description 1
- 108010083879 xyloglucan endo(1-4)-beta-D-glucanase Proteins 0.000 description 1
- 239000002888 zwitterionic surfactant 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
- C11D11/00—Special methods for preparing compositions containing mixtures of detergents
- C11D11/02—Preparation in the form of powder by spray drying
-
- 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
-
- C—CHEMISTRY; METALLURGY
- C11—ANIMAL OR VEGETABLE OILS, FATS, FATTY SUBSTANCES OR WAXES; FATTY ACIDS THEREFROM; DETERGENTS; CANDLES
- C11D—DETERGENT COMPOSITIONS; USE OF SINGLE SUBSTANCES AS DETERGENTS; SOAP OR SOAP-MAKING; RESIN SOAPS; RECOVERY OF GLYCEROL
- C11D3/00—Other compounding ingredients of detergent compositions covered in group C11D1/00
- C11D3/02—Inorganic compounds ; Elemental compounds
- C11D3/04—Water-soluble compounds
- C11D3/044—Hydroxides or bases
-
- C—CHEMISTRY; METALLURGY
- C11—ANIMAL OR VEGETABLE OILS, FATS, FATTY SUBSTANCES OR WAXES; FATTY ACIDS THEREFROM; DETERGENTS; CANDLES
- C11D—DETERGENT COMPOSITIONS; USE OF SINGLE SUBSTANCES AS DETERGENTS; SOAP OR SOAP-MAKING; RESIN SOAPS; RECOVERY OF GLYCEROL
- C11D3/00—Other compounding ingredients of detergent compositions covered in group C11D1/00
- C11D3/02—Inorganic compounds ; Elemental compounds
- C11D3/04—Water-soluble compounds
- C11D3/046—Salts
-
- C—CHEMISTRY; METALLURGY
- C11—ANIMAL OR VEGETABLE OILS, FATS, FATTY SUBSTANCES OR WAXES; FATTY ACIDS THEREFROM; DETERGENTS; CANDLES
- C11D—DETERGENT COMPOSITIONS; USE OF SINGLE SUBSTANCES AS DETERGENTS; SOAP OR SOAP-MAKING; RESIN SOAPS; RECOVERY OF GLYCEROL
- C11D3/00—Other compounding ingredients of detergent compositions covered in group C11D1/00
- C11D3/02—Inorganic compounds ; Elemental compounds
- C11D3/04—Water-soluble compounds
- C11D3/08—Silicates
-
- C—CHEMISTRY; METALLURGY
- C11—ANIMAL OR VEGETABLE OILS, FATS, FATTY SUBSTANCES OR WAXES; FATTY ACIDS THEREFROM; DETERGENTS; CANDLES
- C11D—DETERGENT COMPOSITIONS; USE OF SINGLE SUBSTANCES AS DETERGENTS; SOAP OR SOAP-MAKING; RESIN SOAPS; RECOVERY OF GLYCEROL
- C11D3/00—Other compounding ingredients of detergent compositions covered in group C11D1/00
- C11D3/02—Inorganic compounds ; Elemental compounds
- C11D3/04—Water-soluble compounds
- C11D3/10—Carbonates ; Bicarbonates
-
- 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
- C11D1/29—Sulfates of polyoxyalkylene ethers
-
- 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
- C11D3/122—Sulfur-containing, e.g. sulfates, sulfites or gypsum
-
- 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
- C11D3/1233—Carbonates, e.g. calcite or dolomite
Definitions
- the present invention relates to a process for preparing of a particulate, free flowing detergent particle by a slurry making and spray drying technique.
- the spray-dried particle is suitable for use as a solid laundry detergent composition, or for incorporation into a solid laundry detergent composition.
- granular or particulate laundry detergent composition is prepared by spray drying.
- the detergent components such as surfactants and builders are mixed with around 20% to 50% by weight water to form an aqueous slurry, the aqueous slurry is maintained at temperatures ranging from 60°C to 85°C and then spray-dried in a spray-drying tower.
- anionic surfactants are often added in their acid form.
- linear alkylbenzene sulphonate which is the most commonly used anionic surfactant, is much easier to handle, store and transport in their acid form as compared to the neutralised form.
- the acid precursor of anionic surfactant is then converted in-situ into their corresponding surfactant salt by neutralisation with either aqueous or dry neutralising agents.
- the neutralizing agent employed during the process for preparing a detergent slurry generally include strong alkaline ingredients such as sodium or potassium hydroxide. These alkaline neutralizing agents are used as stoichiometrically required to ensure complete neutralization of the acid form of the anionic surfactant.
- other alkaline salts such as alkali metal silicates and alkali metal carbonates are also added to the detergent slurry. These alkali metal silicates and alkali metal carbonates act as builders and also add alkalinity and add to the buffering capacity in the laundry composition.
- Alkaline ingredients contribute towards good detergency. However, excess alkali in the laundry detergent composition has certain disadvantages. Highly alkaline laundry detergent compositions are harsh on the skin especially in composition designed for hand laundering.
- Silicate salt which is typically a sodium salt of silicate is generally considered a critical ingredient in spray- dried particulate detergent compositions and serves to provide stability and integrity to the detergent particles or agglomerated particles formed during the spray-drying operation.
- attempts at reduction or elimination of sodium silicate has resulted in spray-dried particle with deterioration of flow properties and an increase in caking tendency.
- alkaline builders particularly alkali metal silicates and alkali metal carbonates
- compositions which are milder on hand without adversely affecting the cleaning performance and the powder properties such as free-flowability and extended storage life of spray-dried detergent particle or granular laundry detergent composition including these spray-dried detergent particle.
- WO 98/11193 discloses a process for preparing a granular detergent composition in which an acid precursor of anionic surfactant is partially neutralized followed by fully neutralizing in a high-speed mixer.
- the partial neutralization is by using alkali hydroxide followed by complete neutralization with using a weak alkaline material.
- EP 3146034 B1 discloses a two-stage neutralization process to form detergent granules with improved surfactant activity and good particulate flowability.
- the process includes a first step of neutralizing 5% to 20% of the acid precursor of the surfactant with a neutralizing agent and then neutralizing the remaining acid precursor with a second neutralizing agent.
- This discloses an agglomeration process and a dry-neutralization which is different from a spray-drying process for preparing a solid detergent particle.
- EP2870229 B1 discloses a process for preparing a detergent granule having at least 50 wt.% anionic surfactant which includes the step of (i) mixing an anionic surfactant precursor with a source of alkali to form a neutralized paste (ii) adding sodium citrate, up to 5 wt.% alkaline silicate and sodium carbonate to form a slurry (iii) spray drying the slurry to form a detergent granule.
- EP2841553 B1 discloses a process for preparing a detergent granule having at least 40 wt.% anionic surfactant which including the step of (i) neutralizing an anionic surfactant precursor with a source of alkali (ii) adding polycarboxylate polymer, sodium sulphate and sodium carbonate to form a slurry (iii) spray drying the slurry to form a detergent granule.
- US 2011/147962 A1 discloses a process for preparing a spray-dried detergent powder having the step of forming an aqueous slurry, transferring the aqueous detergent slurry through a pump to a spray nozzle followed by contacting alkoxylated anionic detersive surfactant and then spraying to form a spray-dried powder. This again, discloses the neutralization of the anionic surfactant in a single step process.
- the present inventors have found a way to provide a free-flowing spray-dried detergent particle which is gentle on hand, gives good fabric care performance, good fabric cleaning performance and which also retains good powder properties by providing a process of preparing a detergent solution which yields lower reserve alkalinity in the spray-dried particle and has a pH preferably from 10.5 to 11.5 and preferably without impacting the current level of alkaline builders such as sodium carbonate and sodium silicate in the composition.
- the present inventors While reducing the amount of unreacted sodium hydroxide in the spray-dried detergent particle is required to address the issue of harshness on hands, the present inventors have found that there is a need for a careful balance between the amount of the LAS acid that is reacted with the first neutralizing agent and the second neutralizing agent to ensure that the fully neutralized solution has desired viscosity for proper mixing and spray drying.
- the selection of specific second neutralizing agent and the careful balance between the portion of acid precursor neutralized by the first and the second neutralizing agent gives the spray dried particle the desired mildness on skin while maintaining good powder properties and good cleaning performance.
- the present invention discloses a process for preparing a a spray-dried detergent particle, wherein the process for preparing the spray-dried detergent particle involves the steps of: i) mixing an acid precursor of an anionic surfactant and an alkali metal hydroxide neutralizing agent in an aqueous medium to form a partially neutralized solution, wherein the partially neutralised solution comprises an anionic surfactant salt formed in-situ by the reaction of a portion of acid anionic surfactant precursor with the alkali metal hydroxide neutralizing agent and said anionic surfactant salt forms 10 parts to 98 parts of the total in-situ anionic surfactant content by weight of the spray-dried detergent particle; and, ii) contacting the partially neutralized solution with a silicate neutralizing agent, wherein the silicate neutralizing agent is provided in an amount sufficient for neutralizing the remaining part of the acid precursor of an anionic surfactant to form a fully neutralized detergent solution; iii) adding laundry ingredients to the fully neutralized
- the fully neutralized solution is mixed with one or more laundry ingredients selected from carbonate-based builder; additional surfactant, a carboxylate polymer, fillers selected from the group consisting of alkali metal sulphate, alkali metal chloride, alkaline earth metal carbonate, or mixtures thereof, more preferably the filler is selected from sodium chloride, sodium sulphate, magnesium carbonate, calcium carbonate, calcite mineral, calcium magnesium carbonate (dolomite) to form a detergent slurry;
- the term “reserve alkalinity” refers to the grams of NaOH/100 grams when titrated till 10 pH with HaSCU. The alkali reserve is determined by an acid/base titration of a solution with 0.5 mol/l sulphuric acid till pH of 10.00.
- the reserve alkalinity of the spray-dried detergent particle to pH 10 is from 1.5 to 5 grams NaOH/100g. Preferably less than 5.0 grams NaOH/100g, preferably less than 4 grams NaOH/100g, still preferably 3.5 grams NaOH/100g, further preferably less than 2 grams NaOH/100g.
- absolute value refers to the amount of Na LAS in the spray-dried detergent particle formed by neutralizing with the silicate neutralizing agent. For example, in a spray-dried detergent particle where the total NaLAS is 20 wt.% of which 5 wt.% is formed by silicate neutralizing agent, then 5 wt.% is the absolute value of NaLAS formed by neutralizing with silicate neutralizing agent and 15 wt.% is the absolute value of NaLAS neutralized by alkali metal neutralizing agent.
- a process for preparing a spray-dried detergent particle comprising the steps as described herein below.
- a process for preparing a spray-dried detergent particle involving the step of mixing a liquid acid precursor of an anionic surfactant and an alkali metal hydroxide neutralizing agent to form a partially neutralized solution.
- the partially neutralised solution includes an anionic surfactant salt formed in-situ by the reaction of a portion of the acid anionic surfactant precursor with the alkali metal hydroxide neutralizing agent.
- the neutralized anionic surfactant salt formed in this step provides 10 parts to 98 parts of the total anionic surfactant content by weight of the spray-dried detergent particle.
- Suitable liquid acid precursor of anionic surfactant are well known to those skilled in the art.
- suitable acid precursor of anionic surfactant includes alkyl and aryl sulphonic acids and derivatives thereof, preferably alkylbenzene sulphonic acid, particularly linear alkylbenzene sulphonic acid having an alkyl chain length of Cs to C22, preferably C10 to C20, still preferably Cn to C15; primary and secondary alkyl sulphuric acid, particularly C12 to C15 primary alkyl sulphuric acid.
- the liquid acid precursor of anionic surfactant is an alkyl benzene sulphonic acid, preferably linear alkylbenzene sulphonic acid (LAS acid or HLAS), more preferably having an alkyl chain length of Cs to C20, still preferably C10 to C20. It is highly preferred that the liquid acid precursor of the anionic surfactant comprises an alkyl benzene sulphonic acid (linear or branched), preferably Cs to C20 linear alkyl benzene sulphonic acid. Preferably the alkyl benzene sulphonic acid is linear or branched, substituted or unsubstituted, Cs to C20 alkyl benzene sulphonate.
- LAS acid or HLAS linear alkylbenzene sulphonic acid
- the alkyl benzene sulphonic acid is linear or branched, substituted or unsubstituted, Cs to C20 alkyl benzene sulphonate.
- Cs to C20 alkyl benzene sulphonic are linear C10 to Ci3 alkylbenzene sulphonic acid.
- linear C10 to C13 alkylbenzene sulphonic acid obtained, by sulphonating commercially available linear alkyl benzenes (LAB);
- suitable LAB include low 2-phenyl LAB, such as those supplied by Sasol under the tradename Isochem® or those supplied by Petresa under the tradename Petrelab®, other suitable LAB include high 2-phenyl LAB, such as those supplied by Sasol under the tradename Hyblene®.
- the anionic surfactant precursor is LAS acid which yields the corresponding linear alkyl benzene sulphonate (LAS) upon neutralisation.
- the acid precursors which includes alkyl ether sulphuric acid; olefin sulphonic acid (preferably Cs to C24; alkyl xylene sulphonic acid; alkane sulphonic acid, dialkyl sulphosuccinic acid; fatty acid ester sulphonic acid and mixtures thereof.
- the acid precursor of anionic surfactant is a non-soap anionic surfactant acid precursor.
- the acid precursor of anionic surfactant has a purity of 85% to 99%, that is it comprises from 90% to 98% acid precursor of anionic surfactant, the remaining ingredients include liquid carrier (water or other inorganic solvent), sulphuric acid, non detergent organic matter such as unreacted linear alkyl benzene. More preferably the acid precursor of anionic surfactant has a purity from 90% to 98%.
- the liquid acid precursor of anionic surfactant is aqueous.
- the acid precursor of the anionic surfactant is preferably provided in a liquid form that is pumpable and suitable for a spray-drying process.
- such acid precursor of anionic surfactant is characterized by a viscosity ranging from about 0.1 Pa.S to about 10 Pa.S, preferably from about 0.1 Pa.S to about 5 Pa.S, more preferably from about 0.2 Pa.S to about 0.5 Pa.S, when measured at 50°C and at a shear rate of 25s 1 .
- the amount of acid precursor of anionic surfactant present in step (i) is sufficient to provide a spray-dried detergent particle having from 5 wt.% to 50 wt.% of the in-situ formed salt of the anionic surfactant, still preferably from 7 wt.% to 50 wt.%, and most preferably from 10 wt.% to 50 wt.% in-situ formed anionic surfactant by weight of the spray dried detergent particle.
- the alkali metal hydroxide neutralizing agent employed during the first neutralization step in accordance with the process of the present invention for partially neutralizing the liquid acid precursor of the anionic surfactant is preferably selected from sodium hydroxide or potassium hydroxide, most preferably the alkali metal hydroxide neutralizing agent according to the present invention is sodium hydroxide.
- the sodium hydroxide is available in the form of an aqueous solution.
- the reaction of an alkali metal hydroxide and acid precursor also yields some water as a by-product.
- the aqueous sodium hydroxide solution has a concentration in the range from 40 wt.% to 50 wt.%.
- the sodium hydroxide has a concentration of at least a 30 wt.% in the aqueous solution.
- anhydrous sodium hydroxide flakes may be used but with extensive safety precautions from chemical spillages or exothermic reactions.
- the mixing of a liquid acid precursor of an anionic surfactant and the alkali metal hydroxide neutralizing agent may be carried out in any suitable mixer. This is typically done in a crutcher mixer with an efficient solid to liquid mixing profile. The most preferred order of addition for this process involves adding water and the alkali metal hydroxide with continuous agitation. The temperature of this solution can be increased optionally by direct or indirect steam heating. This is followed by addition of the liquid acid precursor of the anionic surfactant to the crutcher mixer, with a controlled rate of addition while the reaction mass is under continuous agitation. Preferably it is required to maintain the temperature of the reaction mix in such a manner so as to prevent overflow or boil out of the reaction mass in the crutcher.
- the temperature of the partially neutralized solution formed in step (i) is typically maintained above 50°C, preferably above 60°C and most preferably above 70°C, but preferably below 95 °C and most preferably below 85 °C. It can be preferred that the temperature of the partially neutralized solution so formed is carefully monitored and controlled by the degree of partial neutralization, either alone or in combination with additional heating and cooling means if necessary.
- the total reaction time for the partial neutralization of the liquid acid precursor of anionic surfactant in step (i) can range from 1 minute to 10 minutes preferably depending on the anionic active content present in the detergent solution. In some cases the reaction time can be higher and will not have any impact on the process.
- the mixing time of the acid precursor of anionic surfactant and the alkali metal hydroxide neutralizing agent to attain the neutralization is from 1 to 5 minutes, preferably 1 to 3 minutes, still preferably for 1 to 2 minutes.
- the neutralization time is less than 5 minutes, preferably less than 3 minutes and still preferably less than 2 minutes.
- the alkali metal hydroxide neutralizing agent added is in an amount sufficient to react with a portion of the acid precursor of anionic surfactant which yields from 10 parts to 98 parts of the total in-situ formed anionic surfactant present in the spray-dried detergent particle, more preferably from 21 parts to 98 parts of the total in-situ formed anionic surfactant present in the spray dried detergent particle.
- the alkali metal hydroxide neutralizing agent added is in an amount sufficient to react with a portion of the acid precursor of anionic surfactant which yields at least 21 parts, still preferably at least 22 parts, still preferably at least 23 parts, most preferably at least 24 parts of the total in-situ formed anionic surfactant present in the spray-dried detergent particle, but typically not more than 95 parts, still preferably not more than 90 parts, still further preferably not more than 85 parts, still more preferably not more than 80 parts and most preferably not more than 50 parts of the total in-situ formed anionic surfactant present in the spray-dried detergent particle.
- the process according to the first aspect of the present invention forms a partially neutralized solution in step (i), wherein the partially neutralized solution comprises: i) a salt of anionic surfactant (formed by the reaction between a portion of the acid precursor of the anionic surfactant and the alkali metal hydroxide); ii) the remaining part of the liquid acid precursor of anionic surfactant; and, iii) at least 35 wt.%. water.
- the partially neutralized detergent solution is then an aqueous mixture of the surfactant acid (acid precursor of the anionic surfactant) and neutralised salt form of the anionic surfactant.
- Step ii Forming the fully neutralized detergent solution
- the silicate neutralizing agent is provided in an amount sufficient for neutralizing the remaining part of the liquid acid precursor of an anionic surfactant to form a fully neutralized detergent solution.
- the silicate neutralizing agent is provided in a stoichiometrically excess amount in relation to the remaining part of the liquid acid precursor of an anionic surfactant to form a fully neutralized detergent solution. More preferably the ratio of the silicate neutralizing agent to the anionic surfactant salt formed from the neutralization of the remaining part of the liquid acid precursor in the spray dried detergent particle is from 5 to 30. Preferably the amount of silicate neutralizing agent is in excess of the amount of anionic surfactant salt formed in the spray-dried particle from the remaining liquid acid precursor surfactant available in the partially neutralized solution.
- the amount of the liquid acid precursor of anionic surfactant remaining in the partially neutralized solution is in an amount sufficient to provide from 1 wt.% to 7 wt.% of the total in-situ anionic surfactant salt content (absolute value) present in the spray-dried detergent particle.
- the anionic surfactant salt formed by the neutralization of the remaining part of the acid precursor of an anionic surfactant with the silicate neutralizing agent comprises from 1 wt.% to 7 wt.% of the total anionic surfactant salt present in the spray- dried detergent particle (absolute value), still preferably from 1 wt.% to 6 wt.% and still further preferably from 1 wt.% to 5 wt.% of the total anionic surfactant salt (in absolute value) present in the spray-dried detergent particle.
- the mixing of the partially neutralized solution and silicate neutralizing agent may be carried out in any suitable mixer as described in detail hereinabove in the discussion for mixing liquid acid precursor of anionic surfactant and the alkali metal hydroxide neutralizing agent in step (i).
- Silicate neutralizing agent is employed during the second neutralization stage according to the process of the first aspect of present invention, to neutralize the remaining liquid acid anionic surfactant precursor to form the fully neutralizing detergent solution.
- the silicate neutralizing agent can be any silicate alkali component that is capable of reacting in-situ with the acid precursor of the anionic surfactant to form the anionic surfactant in an appropriate salt form.
- Non-limiting examples of the silicate neutralizing agent includes alkali metal silicates, alkaline earth metal silicates or mixtures thereof.
- alkali metal silicate Preferably the silicate may be selected from sodium silicate, potassium silicate, sodium-potassium double silicate, lithium silicate or mixtures thereof are particularly preferred. More preferably silicate neutralizing agent is sodium silicate.
- the silicate neutralizing agent may be liquid or solid form, preferably they may be crystalline silicates or soluble amorphous silicates.
- the silicate neutralizing agent is preferably a liquid silicate neutralizing agent having an approximate ratio of alkali oxide to silicon dioxide (M2O to S1O2) of 1 : 1.6 to 1:3.3, preferably 1:1.6 to 1:2.85, still preferably from 1:2 to 1:2.85 and most preferably 1:2 to 1:2.7.
- Orthosilicate, having the formula M4S1O4 is the most alkaline having a M2O to S1O2 ratio of 2:1.
- Metasilicate, M2S1O3 has a M2O to S1O2 ratio of 1:1.
- the so called “water glass” silicates which are soluble in water, have a M2O to S1O2 ratio of 1:1.6 to 1 :3.3, preferably silicate with a M2O to S1O2 ratio of from 1 :2.0 to 1 :2.7 where M is an alkaline earth metal, alkali metal, preferably alkali metal. Most preferably the M is sodium (Na).
- the reaction time involving the mixing of the partially neutralized solution and the silicate neutralizing agent is from 1 to 5 minutes, preferably 1 to 3 minutes, still preferably for 1 to 2 minutes to obtain the fully neutralized detergent solution.
- the process according to the first aspect of the present invention forms a fully neutralized detergent solution after step (ii), wherein the fully neutralized detergent solution comprises: i) in-situ formed salt of anionic surfactant; ii) at least 40 wt.% water; and, iii) silicate salt.
- the fully neutralized detergent solution is an aqueous solution having at least 40 wt.% water, still preferably having at least 45 wt.% water, still preferably having at least e 50 wt.% water and typically from 40 wt.% to 65 wt.% water..
- the pH of the fully neutralized detergent solution when measured using a 1 wt.% solution in distilled water at 25°C ranges from 10.5 to 11.5, preferably ranging from 10.8 to 11.2.
- the fully neutralized detergent solution may be spray dried to form the spray dried particle.
- Alternately preferred laundry ingredients which are thermally stable may be added to the fully neutralized detergent solution to form an aqueous detergent slurry before spray-drying.
- aqueous detergent slurry used herein refers to the aqueous mixture obtained by adding the below described laundry ingredients such as builders, filler, optional ingredients to the fully neutralized detergent solution.
- the laundry ingredient may be a builder which may be added post full neutralization of the acid anionic precursor.
- the builders may be preferably selected from precipitation builder, complexing builder, sequestering builders, ion-exchange builder or mixtures thereof.
- the sequestering builder materials added to the fully neutralized detergent solution before spray drying include inorganic sequestering material and/or organic sequestering material.
- Example of the inorganic sequestering material include alkali metal polyphosphates, such as sodium tripolyphosphate.
- Example of the organic sequestering material include ethylene diamine tetra-acetic acid.
- precipitating builder materials include sodium carbonate.
- the preferred complexing builder includes diethylenetriamine-pentaacetic acid, alkyl- or alkenylsuccinic acid, nitrilotriacetic acid as suitable examples.
- ion-exchange builder materials include the various types of water-insoluble crystalline or amorphous aluminosilicates, of which zeolites are the best known representatives, e.g. zeolite A, zeolite B (also known as zeolite P), zeolite C, zeolite X, zeolite Y and also the zeolite P- type as described in EP-A-0,384,070.
- the builder is a carbonate salt builder.
- the carbonate salt builder includes alkaline earth metal and alkali metal carbonates or mixtures thereof.
- the carbonate salt is preferably an alkali metal carbonate, alkaline earth metal carbonate or mixtures thereof.
- Preferred alkali metal carbonates are sodium and/or potassium carbonate of which sodium carbonate is particularly preferred. It is further preferred that sodium carbonate makes up at least 75 wt.%, more preferably at least 85 wt.% and even more preferably at least 90 wt.% of the total weight of the carbonate salt.
- the aqueous detergent slurry may include an organic builder.
- organic builder include polycarboxylate polymers such as polyacrylates, acrylic/maleic copolymers, and acrylic phosphinates; monomeric polycarboxylates such as citrates, gluconates, oxydisuccinates, glycerol mono-, di-and trisuccinates, carboxymethyloxysuccinates, carboxymethyloxymalonates, dipicolinates, hydroxyethyliminodiacetates, alkyl- and alkenylmalonates and succinates; and sulphonated fatty acid salts.
- polycarboxylate polymers such as polyacrylates, acrylic/maleic copolymers, and acrylic phosphinates
- monomeric polycarboxylates such as citrates, gluconates, oxydisuccinates, glycerol mono-, di-and trisuccinates, carboxymethyloxysuccinates, carboxymethyloxymalonates, dip
- the organic builder is selected from monomeric polycarboxylates such as citrates, gluconates, oxydisuccinates, glycerol mono-, di-and trisuccinates, carboxymethyloxysuccinates, carboxymethyloxymalonates, dipicolinates, hydroxyethyliminodiacetates, alkyl- and alkenylmalonates and succinates, more preferably alkali metal citrate, most preferably it is sodium citrate.
- Organic builders may be used in minor amounts as supplement to carbonate builder.
- Preferred supplementary organic builders are citrates, suitably used in amounts of from 0.1 wt.% to 30 wt.% more preferably of alkaline metal compounds, preferably from 10 wt.% to 25 wt.%; and acrylic polymers, more especially acrylic/maleic copolymers, suitably used in amounts of from 0.5 wt.% to 15 wt.%, preferably from 1 wt.% to 10 wt.%.
- the aqueous detergent slurry includes an acrylic maleic copolymer.
- Powder flow properties may be improved by the incorporation of a small amount of a powder structurant, for example, a fatty acid (or fatty acid soap), a sugar, an acrylate or acrylate/maleate polymer.
- a powder structurant for example, a fatty acid (or fatty acid soap), a sugar, an acrylate or acrylate/maleate polymer.
- One preferred powder structurant is acrylic-maleic copolymer, suitably
- Inorganic phosphate builders are preferably present at relatively low levels, for example less than 5 wt.%, still preferably less than 3 wt.%, further preferably less than 1 wt.%.
- the spray-dried detergent particle prepared from the process according to the first aspect of the present invention is substantially free of inorganic phosphate builders.
- substantially free it is meant that the spray dried particle prepared according to the process of the first aspect does not include any deliberately added inorganic phosphate builder.
- the slurry includes 0 wt.% inorganic phosphate builder.
- the spray-dried detergent particle includes 0 wt.% inorganic phosphate builder.
- the zeolite builders are preferably present at relatively low levels, for example less than 5 wt.%, still preferably less than 3 wt.%, further preferably less than 1 wt.% in the aqueous slurry.
- the spray-dried detergent particle prepared from the process according to the first aspect of the present invention is substantially free of zeolite builders. By substantially free it is meant that the spray dried particle prepared according to the process of the first aspect does not include any deliberately added inorganic zeolite builder. Filler:
- the laundry ingredient may be a filler
- the filler may be added to the fully neutralized detergent solution to form an aqueous slurry.
- a filler may be added to the aqueous detergent slurry before or after the carbonate builder addition, preferably before the carbonate builder addition but before spray-drying.
- the filler acts as a balancing ingredient and can be a neutral inorganic salt, mineral or mixtures thereof.
- the filler is selected from the group consisting of alkali metal sulphate, alkali metal chloride, alkaline earth metal carbonate or mixtures thereof.
- the fillers are selected from the group consisting of sodium sulphate, magnesium sulphate, calcium magnesium carbonate (dolomite), calcite, sodium chloride or calcium carbonate, magnesium carbonate or mixtures thereof.
- the filler is sodium sulphate, sodium chloride, calcium carbonate (calcite) or mixtures thereof. More preferably the filler may be preferably sulphate, carbonate salt, sodium chloride or a mixture thereof.
- pre-neutralized surfactant may be preferably added to the fully neutralized detergent solution these include but are not limited to LAS salt, primary alkyl sulphate (PAS), secondary alkyl sulphate (SAS), sodium lauryl ether sulphate (SLES) or combinations thereof.
- PAS primary alkyl sulphate
- SAS secondary alkyl sulphate
- SLES sodium lauryl ether sulphate
- the pre-neutralized surfactant is added as a co surfactant and preferably is present in an amount ranging from 0 wt.% to 20 wt.% by weight of the spray dried particle.
- the co-surfactant is PAS, SLES or combinations thereof.
- aqueous detergent slurry which includes but are not limited to, any one or more of the following: soap, sequestrants, calcium chloride, sodium bicarbonate, other inorganic salts, fluorescers, dyes, anti-redeposition agents such as sodium carboxy methyl cellulose, slurry stabilizers such as homopolymers of acrylic acid and copolymers of acrylic acid and maleic acid; ethylene and maleic anhydride, and of vinyl methyl ether and maleic anhydride, usually in salt form; viscosity modifiers, hydrotrope, defoaming agents, antioxidants, colourants, shading dyes and combinations thereof.
- Aqueous detergent slurry is obtained by adding laundry ingredients preferably carbonate salt builder and/or filler to the fully neutralized detergent solution, and preferably the aqueous detergent slurry comprises: i) in-situ formed salt of anionic surfactant; ii) sodium carbonate; iii) silicate salt; iv) filler; v) preferably a pre-neutralized co-surfactant selected preferably from PAS, SLES or mixtures thereof; and, vi) water.
- the aqueous detergent slurry has a water content from 25 wt.% to 40 wt.%, preferably 27 wt.% to 40 wt.%, still preferably 30 wt.% to 35 wt.%.
- the aqueous detergent slurry has a pH ranging from 10.5 to 11.5, when measured using a 1 wt.% solution in distilled water at 25°C.
- the reserve alkalinity of the aqueous detergent slurry/spray-dried detergent particle is 3% to 20% lower than that of a similar formulation made with the conventional process i.e. , a single step neutralisation with a strong alkali metal hydroxide, NaOH.
- the reserve alkalinity of the spray-dried detergent particle prepared in accordance with the present invention has a reserve alkalinity which is at least 3 % lower than the reserve alkalinity of spray-dried detergent particle prepared using a single step neutralization using sodium hydroxide as the neutralizing agent (herein referred to as the conventional process), still preferably lower by at least 4%, still further preferably lower by at least 5%, still further preferably lower by at least 8% but preferably lower by not more than 19%, still preferably lower by not more than 18%, still further preferably lower by not more than 15% as compared to the reserve alkalinity of a spray-dried detergent particle prepared using a single step neutralization using sodium hydroxide as the neutralizing agent (herein referred to as the conventional process).
- the viscosity of the aqueous detergent slurry is from 1 Pa.s to 20 Pa.s (1000 centipoise to 20,000 centipoise) at a temperature of 65°C to 85°C or even somewhat higher at a shear rate of 17 to 18 sec 1 .
- the aqueous detergent slurry is sufficiently fluid to pump it out of the mixing vessel to a spray tower.
- the viscosity of the slurry may preferably be adjusted by manipulating the slurry moisture content or by addition of an organic or inorganic additive.
- Non-limiting examples of the viscosity adjusters are nonionic surfactant, hydrotropes, polyethylene glycol, polypropylene glycol, and inorganic salts.
- the fully neutralized aqueous detergent solution from step (ii) or the aqueous detergent slurry obtained by addition of other laundry ingredients is spray-dried to form a spray-dried detergent particle.
- the spray-drying is carried out using any of the conventional spray drying system known in the art.
- the aqueous slurry is transferred through a pipe system to a pump system consisting of one or more pump and then further to a spray nozzle through which the slurry is released under pressure into a drying tower.
- the pump system includes one or more pump, the pump is preferably a high-pressure pump.
- the pump system includes a first pump which is typically a low-pressure pump, such as a pump that is capable of generating a pressure of from 1 to 10 bar (1 x10 5 to 1x10 6 Pa), this pressure ensures proper flooding of the second pump.
- the second pump is a high-pressure pump, such as a pump that is capable of generating a pressure ranging from 20 bar to 200 bar (2x10 6 Pa to 2x10 7 Pa).
- the aqueous detergent slurry is transferred through bolt catchers, magnetic filters, lump breakers, disintegrators such as the Ritz Mill, during the transfer of the aqueous slurry through the pipe system downstream the pump system/mixer in which the aqueous slurry is formed.
- disintegrator is positioned between the pumps.
- the flow rate of the aqueous detergent slurry along the pipes is typically in the range from 800 kg/hour to more than 75,000 kg/hour.
- the spray drying system may include a deaeration system.
- the deaeration system is preferably a vacuum assisted de-aerator, which is preferably fed by a transfer pump.
- the deaeration system remove air bubbles formed during the slurry preparation, thus increasing the bulk density of the spray-dried detergent particle.
- De-aeration of the slurry may also be carried out by other mechanical means or chemical de-aeration means using antifoams or de-foamers.
- air injection system may be provided along the pipe system.
- the air injection system may be provided before or after the pump system.
- the air injection includes air flow and pressure controls, static mixer, pulsation dampener and compressor set which can aerate the slurry to get a lower bulk density for the spray dried particle.
- a typical spray drying system can optionally include both the de-aeration system and air injection system to optimize the desired bulk density of the spray dried particle.
- Typical spray drying tower for detergent applications are counter-current spray drying tower.
- the inlet hot air/hot steam temperature introduced into the spray drying tower is the range from 150°C to 500°C depending on the evaporation capacity and sizing of the tower.
- the tower exhaust air temperature can range from, 50°C to 200°C, more preferably 80°C to 200°C, still more preferably 80°C to 100°C depending on the loading of the tower.
- the aqueous detergent slurry introduced into the spray nozzle of the spray drying tower is preferably at a temperature ranging from 60°C to 95°C.
- the spray drying tower may be a co-current spray drying tower but are less common.
- the spray-dried powder exiting the spray-drying tower has a temperature of less than 150°C, and still preferably less than to 100°C.
- the spray-drying zone is under a slight vacuum.
- the vacuum is controlled by the speed and/or damper setting of the inlet and outlet air fans.
- the negative pressure in the spray- drying tower can be measured by any available means.
- pressure sensors are present in the spray-drying zone (inside the spray-drying tower).
- the vacuum pressure in the spray drying zone ranges from -10Nnr 2 to -600Nnr 2 , preferably -10Nnr 2 to -300Nnr 2 to improve the cooling of the spray-dried particle.
- the maximum pressure one can use is determined by the structural strength of the spray-drying tower and care must be taken not to exceed this maximum vacuum so that no undue stress is placed on the spray- drying tower.
- the spray-dried detergent particle collected at the bottom of the tower may be subjected to cooling and conditioning by using an air lift or any similar process.
- a flow aid such as zeolite is added to the spray-dried detergent particle before air-lifting.
- the spray-dried detergent particle is subjected to particle size classification to remove oversize material (> 2 mm typically) to provide a spray dried detergent particle which is free flowing.
- the fine material ⁇ 100 microns typically
- the spray-dried detergent particle may itself be used as fully formulated laundry composition.
- further laundry ingredients are dry-added to the spray-dried detergent particle to form a fully formulated laundry detergent composition
- this dry addition of further laundry ingredient to the spray-dried particle is generally termed as post-dosing.
- a spray-dried detergent particle obtainable by a process of the first aspect.
- the spray-dried detergent particle according to the second aspect of the present invention includes: i) from 5 wt.% to 50 wt.% in-situ neutralized anionic surfactant; ii) optionally from 0 wt.% to 20 wt.% co-surfactant, preferably selected from PAS, SLES or mixtures thereof; iii) from 8 wt.% to 20 wt.% silicate salt, preferably with a SiC NaaO weight ratio from 1:1.6 to 3.3, iv) preferably from 8 wt.% to 70 wt.% carbonate salt; v) optionally, from 2 wt.% to 10 wt.% magnesium sulphate; vi) optionally, from 0.5 wt.% to 5 wt.% polymer; vii) optionally, from 1 wt.% to 65 wt.% filler, preferably selected from sodium sulphate, sodium carbonate, sodium chloride, alkaline earth metal carbon
- the amount of water present in the spray dried particle is from 0 wt.% to 4.5 wt.%, preferably 0 wt.% to 4 wt.%.
- the spray-dried detergent particle formed by spray drying the fully neutralized detergent solution or the aqueous slurry preferably comprises from 7 wt.% to 50 wt.% in-situ formed anionic surfactant salt.
- the spray-dried detergent particle has a pH ranging from 10.5 to 11.5 when measured using a 1 wt.% solution with distilled water at room temperature.
- the spray-dried detergent particle has a reserve alkalinity which is 3% to 20% lower than that of a similar formulation made with the conventional process i.e., a single step neutralisation with a strong alkali metal hydroxide, NaOH.
- the spray-dried detergent particle has a bulk density of less than 550g/L.
- the spray-dried detergent particle has a weight average particle size of from 300 micrometers to 600 micrometers.
- the spray-dried detergent particle preferably comprises from 7 wt.% to 50 wt.% anionic surfactants, which is preferably a Cio to C2 0 linear alkyl benzene sulphonate and which is substantially neutralized with little or no acid residues.
- the spray-dried particle is typically post dosed with ingredients that are incompatible with the spray-drying process conditions to form a fully formulated laundry detergent composition. These components may be incompatible for many reasons including heat sensitivity, pH sensitivity or degradation in aqueous systems.
- the composition of the spray-dried detergent particle includes from 8 wt.% to 20 wt.% alkali metal silicate builder, preferably from 8 wt.% to 70 wt.% alkali metal carbonate builder, still preferably from 8 wt.% to 30 wt.% alkali metal carbonate builder.
- the spray dried detergent particle may further include cellulose derivatives, acetates, polyacrylates, acrylate-maleate copolymers, magnesium sulfate and mixtures thereof.
- the spray-dried detergent particle may be used as a fully formulated laundry detergent composition or may be additionally combined with other optional benefit ingredients to form a fully formulated laundry detergent composition.
- the optional post dosed benefit ingredients includes but is not limited to enzymes, anti redeposition polymers, perfumes, additional surfactant selected from amphoteric surfactant, zwitterionic surfactant, cationic surfactant and non-ionic surfactant, optical brighteners, antifoaming agent, foam boosters, fabric softeners such as smectite clays, amine softeners and cationic softeners; bleach and bleach activators; dyes or pigments, fillers, fluorescers, salts, soil release polymers, dye transfer inhibitors.
- These optional ingredients are well known to be used in a laundry detergent composition and added preferably by post-dosing.
- Non-limiting examples of the post-dosed polymers include cleaning polymers, antiredeposition polymers, soil release polymers structuring polymers. Some examples include PET-PEOT polymer (Repel-o-Tex® SF2 ex.Solvay), copolymer of acrylic acid and maleic acid (Sokalan CP5 ex. BASF).
- Suitable fluorescent brighteners include dis-styryl biphenyl compounds example Tinopal® CBS-X, di-amino stilbene di-sulfonic acid compounds, e.g. Tinopal® DMS pure Xtra and Blankophor® HRH, and Pyrazoline compounds, e.g. Blankophor® SN, and coumarin compounds, e.g. Tinopal® SWN.
- Preferred brighteners are: sodium 2 (4- styry)-3-sulfophenyl)-2H-napthol(1,2-d]triazole, disodium 4,4’bis ⁇ [4-anilino-6-(N methyl- N-2 hydroxyethyl)amino 1,3,5- triazin-2-yl)]amino]stilbene-2-2' disulfonate, disodium 4,4’bis([(4-anilino-6-morpholino-l,3,5-triazin-2-yl)]amino ⁇ stilbene-2-2'disulfonate, and disodium 4,4’- bis(2-sulfostyryl)biphenyl.
- a suitable fluorescent brightener is S C.l.
- Fluorescent Brightener 260 which may be used in its beta or alpha crystalline forms, or a mixture of these forms.
- the composition of the present invention preferably includes an enzyme. It may preferably include one or more enzymes. Preferred examples of the enzymes include those which provide cleaning performance and/or fabric care benefits.
- Suitable enzymes include, but are not limited to, hemicellulases, peroxidases, proteases, cellulases, xylanases, lipases, xyloglucanase, phospholipases, esterases, cutinases, pectinases, mannanases, pectate lyases, keratinases, reductases, oxidases, phenoloxidases, lipoxygenases, ligninases, pullulanases, tannases, pentosanases, mannanases, G-glucanases, arabinosidases, hyaluronidase, chondroitinase, laccase, and amylases, or mixtures thereof.
- a typical combination is an enzyme combination that includes a protease and lipase in conjunction with one or more of amylase, mannanase and cellulase.
- the enzymes When present in a detergent composition, the enzymes may be present at levels from about 0.00001% to about 2%, from about 0.0001% to about 1% or from 0.001% to about 0.5% enzyme protein by weight of the detergent composition.
- the spray dried detergent particle or a laundry composition having the spray dried detergent particle prepared according to the invention may be packaged as unit doses in polymeric film soluble in the wash water.
- the spray-dried detergent particle or a composition including the particle of the invention may be supplied in multidose plastics packs with a top or bottom closure.
- a dosing measure may be supplied with the pack either as a part of the cap or as an integrated system.
- the packaging material suitable for packaging may include but not limited to multilayer polyethylene film, laminate, paper based, and other materials known to a person skilled in the art.
- the packaging material is selected from material which are biodegradable or recyclable.
- a method of laundering fabric using a spray dried detergent particle or a laundry composition comprising a spray dried detergent particle according to the present invention which involves the step of diluting the dose of detergent composition with water to obtain a wash liquor and washing fabrics with the wash liquor so formed.
- the dose of detergent composition is typically put into a dispenser and from there it is flushed into the machine by the water flowing into the machine, thereby forming the wash liquor. From 5 up to about 65 litres of water may be used to form the wash liquor depending on the machine configuration.
- the dose of detergent composition may be adjusted accordingly to give appropriate wash liquor concentrations.
- the dilution step preferably provides a wash liquor which comprises inter alia from about 3 to about 20 g/wash of detersive surfactants (as are further defined above).
- Example 1 Process for preparing a spray-dried detergent particle according to the present invention:
- a batch of 1 tonne of spray-dried detergent particle was prepared using the ingredients as provided in Table 1.
- an aqueous detergent slurry (Ex 1) was prepared by adding required amount of water and caustic acid (NaOH, alkali metal hydroxide neutralizing agent) to the crutcher mixer.
- LAS acid liquid acid precursor of anionic surfactant
- a portion of LAS acid (which formed 75 parts of the total anionic surfactant present in the spray dried detergent particle)was neutralized to form the salt form (NaLAS).
- aqueous detergent slurries (Ex 1, Ex A) were each spray dried in a counter- current spray drying tower.
- the aqueous detergent slurry is maintained at a temperature of 80°C and pumped under a pressure of 3 X 10 6 Nnr 2 , into a counter current spray- drying tower with an air inlet temperature of around 300°C.
- the aqueous slurry is atomised, and the atomised slurry is dried to produce a solid mixture, which is then cooled and sieved to remove oversize material (> 2mm) to form a spray- dried free-flowing particle in the form of a powder.
- the spray-dried (powder) detergent particle has a moisture content of 2 wt.%, a bulk density of 375g/L and a particle size distribution such that greater than 90 wt.% of the spray-dried detergent particle (powder) has a particle size such that greater than 1.4 mm is around 3 wt.% and less than 180 micrometers is less than 15 wt.%.
- the spray dried detergent particle of Ex A and Ex 1 were prepared using same method of slurry making and spray-drying but differed in that in the process of preparing the spray dried particle of Ex A the entire acid precursor of the anionic surfactant was neutralized using only NaOH as the neutralization agent and in the spray-dried detergent particle of Ex 1 the acid precursor of the anionic surfactant was prepared using a first neutralization step using NaOH followed by neutralization with sodium silicate.
- the two spray-dried detergent particle were then analysed for their reserve alkalinity using the following method.
- the reserve alkalinity was determined by an acid titration of a 1% solution of the spray- dried detergent particle with 0.5 mol/l sulphuric acid till pH of 10.00.
- First a 1% aqueous solution of the spray dried particle was prepared by dissolving 20 grams of the spray- dried detergent particle (W) in 1980 mL of distilled water. The prepared aqueous solution (2000 mL) was then titrated with 0.5 mol/l sulphuric acid (t) till a pH of 10 was reached. The amount of titrant (V) was noted.
- Irritancy index indicates degree of harshness of the spray-dried detergent particle on the skin. A lower irritancy index value indicates that the formulation is milder on skin, while higher value indicate that the formulation is harsher on the skin.
- the irritancy index is determined using the formula: pH + (Reserve alkalinity)/6. Compression test This test evaluates the tendency of the powder towards caking. A split cylinder with a polished internal surface is positioned on a firm base to form a hollow cylindrical mould with a diameter of 9 centimetres. Spray dried detergent particle prepared according to the present invention (Ex 1) was filled inside the hollow cylindrical mould and levelled. A plastic disc is placed on levelled spray-dried detergent particle mass.
- a weight of 12 kilogram is slowly placed on the plastic disc in such a way that the weight is uniformly applied on the spray-dried detergent particle mass in the mould and the disc was allowed to compact the spray-dried detergent particle mass to form a compacted cake. After 2 minutes the weight was removed, and the cylindrical mould is opened slowly without disturbing the compacted cake mass. Next, incremental weights of 200 grams is added at an interval of 10 seconds till the compacted cake mass collapses. Total vertical load required to collapse the compacted cake mass is noted and expressed in grams and this amount in grams is indirectly defined as the caking tendency. Higher the value of the vertical load required to collapse the compacted cake mass the greater is the caking tendency of the powder under evaluation. For the present evaluation, values lower than 1 Kilogram is considered good and values beyond 2 Kilogram is classified as cohesive and classified as powder with high caking tendency.
- composition of the spray-dried detergent particle obtained by spray-drying the aqueous detergent slurry is given below.
- Table 2 * measured by preparing a 1 wt.% solution of the spray-dried detergent particle in distilled water at room temperature.
- the data on table 2 shows that the spray-dried detergent particle obtained from a process where the liquid acid detergent precursor is neutralized according to the present invention by employing alkali metal hydroxide neutralizing agent followed by silicate neutralizing agent provides the spray-dried detergent particle (Ex 1) having lowered reserve alkalinity (13.3% lesser reserve alkalinity as compared to the conventional powder of Ex A) whilst maintaining similar pH as that of the conventionally prepared spray dried particle (Ex A, fully neutralized using NaOH), thus providing the spray-dried particle according to the present invention with lowered harshness on hand and/or fabric while maintaining good cleaning performance and powder properties (as shown by a lowered tendency to caking).
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Abstract
Description
Claims
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BR112023024048A BR112023024048A2 (en) | 2021-05-19 | 2022-05-18 | PROCESS FOR PREPARING A SPRAY-DRIED DETERGENT PARTICLE AND SPRAY-DRIED DETERGENT PARTICLE |
EP22729242.2A EP4341370A1 (en) | 2021-05-19 | 2022-05-18 | Process for preparing a spray dried detergent particle |
CN202280035153.2A CN117500901A (en) | 2021-05-19 | 2022-05-18 | Process for preparing spray-dried detergent granules |
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CN (1) | CN117500901A (en) |
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Citations (6)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
EP0384070A2 (en) | 1988-11-03 | 1990-08-29 | Unilever Plc | Zeolite P, process for its preparation and its use in detergent compositions |
WO1998011193A1 (en) | 1996-09-10 | 1998-03-19 | Unilever Plc | Process for preparing high bulk density detergent compositions |
US20110147962A1 (en) | 2009-12-18 | 2011-06-23 | Larry Savio Cardozo | Spray-Drying Process |
US20150337246A1 (en) * | 2014-05-23 | 2015-11-26 | The Procter & Gamble Company | Two-stage neutralization process for forming detergent granules, and products containing the same |
EP2841553B1 (en) | 2012-04-27 | 2018-02-21 | Unilever N.V. | Process for the production of a detergent granule, detergent granule and detergent composition comprising said granule |
EP2870229B1 (en) | 2012-07-09 | 2019-08-07 | Unilever N.V. | Process for the production of a detergent granule, detergent granule and detergent composition comprising said granule |
-
2022
- 2022-05-18 CN CN202280035153.2A patent/CN117500901A/en active Pending
- 2022-05-18 WO PCT/EP2022/063372 patent/WO2022243343A1/en active Application Filing
- 2022-05-18 BR BR112023024048A patent/BR112023024048A2/en unknown
- 2022-05-18 EP EP22729242.2A patent/EP4341370A1/en active Pending
Patent Citations (7)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
EP0384070A2 (en) | 1988-11-03 | 1990-08-29 | Unilever Plc | Zeolite P, process for its preparation and its use in detergent compositions |
WO1998011193A1 (en) | 1996-09-10 | 1998-03-19 | Unilever Plc | Process for preparing high bulk density detergent compositions |
US20110147962A1 (en) | 2009-12-18 | 2011-06-23 | Larry Savio Cardozo | Spray-Drying Process |
EP2841553B1 (en) | 2012-04-27 | 2018-02-21 | Unilever N.V. | Process for the production of a detergent granule, detergent granule and detergent composition comprising said granule |
EP2870229B1 (en) | 2012-07-09 | 2019-08-07 | Unilever N.V. | Process for the production of a detergent granule, detergent granule and detergent composition comprising said granule |
US20150337246A1 (en) * | 2014-05-23 | 2015-11-26 | The Procter & Gamble Company | Two-stage neutralization process for forming detergent granules, and products containing the same |
EP3146034B1 (en) | 2014-05-23 | 2019-07-10 | The Procter and Gamble Company | Two-stage neutralization process for forming detergent granules, and products containing the same |
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