WO1990004630A1 - A process for preparing a detergent slurry and particulate detergent composition - Google Patents
A process for preparing a detergent slurry and particulate detergent composition Download PDFInfo
- Publication number
- WO1990004630A1 WO1990004630A1 PCT/US1989/004603 US8904603W WO9004630A1 WO 1990004630 A1 WO1990004630 A1 WO 1990004630A1 US 8904603 W US8904603 W US 8904603W WO 9004630 A1 WO9004630 A1 WO 9004630A1
- Authority
- WO
- WIPO (PCT)
- Prior art keywords
- weight
- slurry
- alkali metal
- composition
- detergent
- Prior art date
Links
- 239000002002 slurry Substances 0.000 title claims abstract description 186
- 239000003599 detergent Substances 0.000 title claims abstract description 110
- 238000004519 manufacturing process Methods 0.000 title claims abstract description 6
- 239000000203 mixture Substances 0.000 title claims description 111
- 229910001514 alkali metal chloride Inorganic materials 0.000 claims abstract description 54
- 125000000217 alkyl group Chemical group 0.000 claims description 45
- WCUXLLCKKVVCTQ-UHFFFAOYSA-M Potassium chloride Chemical compound [Cl-].[K+] WCUXLLCKKVVCTQ-UHFFFAOYSA-M 0.000 claims description 36
- CDBYLPFSWZWCQE-UHFFFAOYSA-L Sodium Carbonate Chemical compound [Na+].[Na+].[O-]C([O-])=O CDBYLPFSWZWCQE-UHFFFAOYSA-L 0.000 claims description 36
- 239000002736 nonionic surfactant Substances 0.000 claims description 29
- FAPWRFPIFSIZLT-UHFFFAOYSA-M Sodium chloride Chemical compound [Na+].[Cl-] FAPWRFPIFSIZLT-UHFFFAOYSA-M 0.000 claims description 28
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 claims description 27
- 239000003945 anionic surfactant Substances 0.000 claims description 23
- 229910000029 sodium carbonate Inorganic materials 0.000 claims description 20
- 239000001103 potassium chloride Substances 0.000 claims description 17
- 235000011164 potassium chloride Nutrition 0.000 claims description 17
- PMZURENOXWZQFD-UHFFFAOYSA-L Sodium Sulfate Chemical compound [Na+].[Na+].[O-]S([O-])(=O)=O PMZURENOXWZQFD-UHFFFAOYSA-L 0.000 claims description 16
- 229910052938 sodium sulfate Inorganic materials 0.000 claims description 16
- 235000011152 sodium sulphate Nutrition 0.000 claims description 16
- 239000004615 ingredient Substances 0.000 claims description 15
- 230000001603 reducing effect Effects 0.000 claims description 14
- 239000011780 sodium chloride Substances 0.000 claims description 14
- 229910019142 PO4 Inorganic materials 0.000 claims description 13
- 125000004432 carbon atom Chemical group C* 0.000 claims description 12
- 239000000945 filler Substances 0.000 claims description 12
- 238000000034 method Methods 0.000 claims description 11
- 239000000654 additive Substances 0.000 claims description 10
- 238000001035 drying Methods 0.000 claims description 10
- NBIIXXVUZAFLBC-UHFFFAOYSA-K phosphate Chemical compound [O-]P([O-])([O-])=O NBIIXXVUZAFLBC-UHFFFAOYSA-K 0.000 claims description 10
- 239000010452 phosphate Substances 0.000 claims description 10
- 229910000288 alkali metal carbonate Inorganic materials 0.000 claims description 9
- 150000008041 alkali metal carbonates Chemical class 0.000 claims description 9
- 239000010457 zeolite Substances 0.000 claims description 9
- 230000000153 supplemental effect Effects 0.000 claims description 7
- 229910021536 Zeolite Inorganic materials 0.000 claims description 6
- HNPSIPDUKPIQMN-UHFFFAOYSA-N dioxosilane;oxo(oxoalumanyloxy)alumane Chemical compound O=[Si]=O.O=[Al]O[Al]=O HNPSIPDUKPIQMN-UHFFFAOYSA-N 0.000 claims description 6
- 125000002887 hydroxy group Chemical group [H]O* 0.000 claims description 6
- 229910052799 carbon Inorganic materials 0.000 claims description 5
- 230000000996 additive effect Effects 0.000 claims description 4
- 150000001720 carbohydrates Chemical class 0.000 claims description 3
- 125000004429 atom Chemical group 0.000 claims 2
- QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical compound [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 claims 2
- 229910052760 oxygen Inorganic materials 0.000 claims 2
- 239000001301 oxygen Substances 0.000 claims 2
- 239000007921 spray Substances 0.000 claims 1
- BVKZGUZCCUSVTD-UHFFFAOYSA-L Carbonate Chemical compound [O-]C([O-])=O BVKZGUZCCUSVTD-UHFFFAOYSA-L 0.000 abstract description 26
- -1 alkyl glycosides Chemical class 0.000 description 21
- 239000004094 surface-active agent Substances 0.000 description 21
- 239000007787 solid Substances 0.000 description 20
- 238000002156 mixing Methods 0.000 description 19
- 238000009472 formulation Methods 0.000 description 18
- 230000000694 effects Effects 0.000 description 15
- 229930182470 glycoside Natural products 0.000 description 15
- 239000000463 material Substances 0.000 description 14
- 125000000129 anionic group Chemical group 0.000 description 11
- 235000021317 phosphate Nutrition 0.000 description 11
- 239000004115 Sodium Silicate Substances 0.000 description 8
- 229910052911 sodium silicate Inorganic materials 0.000 description 8
- NTHWMYGWWRZVTN-UHFFFAOYSA-N sodium silicate Chemical compound [Na+].[Na+].[O-][Si]([O-])=O NTHWMYGWWRZVTN-UHFFFAOYSA-N 0.000 description 8
- 238000002474 experimental method Methods 0.000 description 7
- 239000011734 sodium Substances 0.000 description 7
- 235000019832 sodium triphosphate Nutrition 0.000 description 6
- 238000002360 preparation method Methods 0.000 description 5
- BVKZGUZCCUSVTD-UHFFFAOYSA-M Bicarbonate Chemical compound OC([O-])=O BVKZGUZCCUSVTD-UHFFFAOYSA-M 0.000 description 4
- 239000002994 raw material Substances 0.000 description 4
- RZVAJINKPMORJF-UHFFFAOYSA-N Acetaminophen Chemical compound CC(=O)NC1=CC=C(O)C=C1 RZVAJINKPMORJF-UHFFFAOYSA-N 0.000 description 3
- BPQQTUXANYXVAA-UHFFFAOYSA-N Orthosilicate Chemical compound [O-][Si]([O-])([O-])[O-] BPQQTUXANYXVAA-UHFFFAOYSA-N 0.000 description 3
- 229910052783 alkali metal Inorganic materials 0.000 description 3
- 239000003795 chemical substances by application Substances 0.000 description 3
- 150000003841 chloride salts Chemical class 0.000 description 3
- 125000002791 glucosyl group Chemical group C1([C@H](O)[C@@H](O)[C@H](O)[C@H](O1)CO)* 0.000 description 3
- 150000003013 phosphoric acid derivatives Chemical class 0.000 description 3
- 238000006116 polymerization reaction Methods 0.000 description 3
- 229940071207 sesquicarbonate Drugs 0.000 description 3
- 238000001694 spray drying Methods 0.000 description 3
- SRBFZHDQGSBBOR-IOVATXLUSA-N D-xylopyranose Chemical compound O[C@@H]1COC(O)[C@H](O)[C@H]1O SRBFZHDQGSBBOR-IOVATXLUSA-N 0.000 description 2
- 101100380569 Neurospora crassa (strain ATCC 24698 / 74-OR23-1A / CBS 708.71 / DSM 1257 / FGSC 987) apg-5 gene Proteins 0.000 description 2
- 150000008055 alkyl aryl sulfonates Chemical class 0.000 description 2
- 150000004649 carbonic acid derivatives Chemical class 0.000 description 2
- GVGUFUZHNYFZLC-UHFFFAOYSA-N dodecyl benzenesulfonate;sodium Chemical compound [Na].CCCCCCCCCCCCOS(=O)(=O)C1=CC=CC=C1 GVGUFUZHNYFZLC-UHFFFAOYSA-N 0.000 description 2
- 150000002338 glycosides Chemical class 0.000 description 2
- 238000010348 incorporation Methods 0.000 description 2
- 239000007788 liquid Substances 0.000 description 2
- 238000004806 packaging method and process Methods 0.000 description 2
- 150000003839 salts Chemical class 0.000 description 2
- 150000004760 silicates Chemical class 0.000 description 2
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N silicon dioxide Inorganic materials O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 description 2
- 239000000344 soap Substances 0.000 description 2
- 229910052708 sodium Inorganic materials 0.000 description 2
- 239000011343 solid material Substances 0.000 description 2
- 238000003756 stirring Methods 0.000 description 2
- 239000000126 substance Substances 0.000 description 2
- 238000012360 testing method Methods 0.000 description 2
- CIOXZGOUEYHNBF-UHFFFAOYSA-N (carboxymethoxy)succinic acid Chemical class OC(=O)COC(C(O)=O)CC(O)=O CIOXZGOUEYHNBF-UHFFFAOYSA-N 0.000 description 1
- 241000331231 Amorphocerini gen. n. 1 DAD-2008 Species 0.000 description 1
- 239000004215 Carbon black (E152) Substances 0.000 description 1
- 229920002134 Carboxymethyl cellulose Polymers 0.000 description 1
- WQZGKKKJIJFFOK-CBPJZXOFSA-N D-Gulose Chemical compound OC[C@H]1OC(O)[C@H](O)[C@H](O)[C@H]1O WQZGKKKJIJFFOK-CBPJZXOFSA-N 0.000 description 1
- WQZGKKKJIJFFOK-WHZQZERISA-N D-aldose Chemical compound OC[C@H]1OC(O)[C@@H](O)[C@@H](O)[C@H]1O WQZGKKKJIJFFOK-WHZQZERISA-N 0.000 description 1
- WQZGKKKJIJFFOK-IVMDWMLBSA-N D-allopyranose Chemical compound OC[C@H]1OC(O)[C@H](O)[C@H](O)[C@@H]1O WQZGKKKJIJFFOK-IVMDWMLBSA-N 0.000 description 1
- HMFHBZSHGGEWLO-SOOFDHNKSA-N D-ribofuranose Chemical compound OC[C@H]1OC(O)[C@H](O)[C@@H]1O HMFHBZSHGGEWLO-SOOFDHNKSA-N 0.000 description 1
- 101100536354 Drosophila melanogaster tant gene Proteins 0.000 description 1
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 1
- IAYPIBMASNFSPL-UHFFFAOYSA-N Ethylene oxide Chemical compound C1CO1 IAYPIBMASNFSPL-UHFFFAOYSA-N 0.000 description 1
- RFSUNEUAIZKAJO-ARQDHWQXSA-N Fructose Chemical compound OC[C@H]1O[C@](O)(CO)[C@@H](O)[C@@H]1O RFSUNEUAIZKAJO-ARQDHWQXSA-N 0.000 description 1
- 229930091371 Fructose Natural products 0.000 description 1
- 239000005715 Fructose Substances 0.000 description 1
- WQZGKKKJIJFFOK-GASJEMHNSA-N Glucose Natural products OC[C@H]1OC(O)[C@H](O)[C@@H](O)[C@@H]1O WQZGKKKJIJFFOK-GASJEMHNSA-N 0.000 description 1
- DGAQECJNVWCQMB-PUAWFVPOSA-M Ilexoside XXIX Chemical compound C[C@@H]1CC[C@@]2(CC[C@@]3(C(=CC[C@H]4[C@]3(CC[C@@H]5[C@@]4(CC[C@@H](C5(C)C)OS(=O)(=O)[O-])C)C)[C@@H]2[C@]1(C)O)C)C(=O)O[C@H]6[C@@H]([C@H]([C@@H]([C@H](O6)CO)O)O)O.[Na+] DGAQECJNVWCQMB-PUAWFVPOSA-M 0.000 description 1
- OFOBLEOULBTSOW-UHFFFAOYSA-N Propanedioic acid Natural products OC(=O)CC(O)=O OFOBLEOULBTSOW-UHFFFAOYSA-N 0.000 description 1
- PYMYPHUHKUWMLA-LMVFSUKVSA-N Ribose Natural products OC[C@@H](O)[C@@H](O)[C@@H](O)C=O PYMYPHUHKUWMLA-LMVFSUKVSA-N 0.000 description 1
- QAOWNCQODCNURD-UHFFFAOYSA-L Sulfate Chemical compound [O-]S([O-])(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-L 0.000 description 1
- 239000004480 active ingredient Substances 0.000 description 1
- 230000002411 adverse Effects 0.000 description 1
- 150000001298 alcohols Chemical class 0.000 description 1
- 229910052910 alkali metal silicate Inorganic materials 0.000 description 1
- 150000001340 alkali metals Chemical class 0.000 description 1
- HMFHBZSHGGEWLO-UHFFFAOYSA-N alpha-D-Furanose-Ribose Natural products OCC1OC(O)C(O)C1O HMFHBZSHGGEWLO-UHFFFAOYSA-N 0.000 description 1
- WQZGKKKJIJFFOK-PHYPRBDBSA-N alpha-D-galactose Chemical compound OC[C@H]1O[C@H](O)[C@H](O)[C@@H](O)[C@H]1O WQZGKKKJIJFFOK-PHYPRBDBSA-N 0.000 description 1
- PYMYPHUHKUWMLA-UHFFFAOYSA-N arabinose Natural products OCC(O)C(O)C(O)C=O PYMYPHUHKUWMLA-UHFFFAOYSA-N 0.000 description 1
- SRBFZHDQGSBBOR-UHFFFAOYSA-N beta-D-Pyranose-Lyxose Natural products OC1COC(O)C(O)C1O SRBFZHDQGSBBOR-UHFFFAOYSA-N 0.000 description 1
- WQZGKKKJIJFFOK-VFUOTHLCSA-N beta-D-glucose Chemical compound OC[C@H]1O[C@@H](O)[C@H](O)[C@@H](O)[C@@H]1O WQZGKKKJIJFFOK-VFUOTHLCSA-N 0.000 description 1
- 230000015572 biosynthetic process Effects 0.000 description 1
- 239000007844 bleaching agent Substances 0.000 description 1
- 238000005282 brightening Methods 0.000 description 1
- 150000001721 carbon Chemical group 0.000 description 1
- 239000001768 carboxy methyl cellulose Substances 0.000 description 1
- 235000010948 carboxy methyl cellulose Nutrition 0.000 description 1
- 239000008112 carboxymethyl-cellulose Substances 0.000 description 1
- 239000013522 chelant Substances 0.000 description 1
- 239000002738 chelating agent Substances 0.000 description 1
- 238000006243 chemical reaction Methods 0.000 description 1
- 239000003086 colorant Substances 0.000 description 1
- 239000008139 complexing agent Substances 0.000 description 1
- 229920001577 copolymer Polymers 0.000 description 1
- 230000007423 decrease Effects 0.000 description 1
- 230000001627 detrimental effect Effects 0.000 description 1
- 235000014113 dietary fatty acids Nutrition 0.000 description 1
- YRIUSKIDOIARQF-UHFFFAOYSA-N dodecyl benzenesulfonate Chemical compound CCCCCCCCCCCCOS(=O)(=O)C1=CC=CC=C1 YRIUSKIDOIARQF-UHFFFAOYSA-N 0.000 description 1
- 229940071161 dodecylbenzenesulfonate Drugs 0.000 description 1
- 238000010981 drying operation Methods 0.000 description 1
- 230000007613 environmental effect Effects 0.000 description 1
- RTZKZFJDLAIYFH-UHFFFAOYSA-N ether Substances CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 description 1
- 238000007046 ethoxylation reaction Methods 0.000 description 1
- 239000000194 fatty acid Substances 0.000 description 1
- 229930195729 fatty acid Natural products 0.000 description 1
- 150000004665 fatty acids Chemical class 0.000 description 1
- 150000002191 fatty alcohols Chemical class 0.000 description 1
- 239000012530 fluid Substances 0.000 description 1
- 239000004872 foam stabilizing agent Substances 0.000 description 1
- 239000003205 fragrance Substances 0.000 description 1
- 229930182830 galactose Natural products 0.000 description 1
- 239000008103 glucose Substances 0.000 description 1
- 229930195733 hydrocarbon Natural products 0.000 description 1
- VZCYOOQTPOCHFL-UPHRSURJSA-N maleic acid Chemical compound OC(=O)\C=C/C(O)=O VZCYOOQTPOCHFL-UPHRSURJSA-N 0.000 description 1
- 239000011976 maleic acid Substances 0.000 description 1
- 229910052751 metal Inorganic materials 0.000 description 1
- 239000002184 metal Substances 0.000 description 1
- 229910021645 metal ion Inorganic materials 0.000 description 1
- 230000007935 neutral effect Effects 0.000 description 1
- MGFYIUFZLHCRTH-UHFFFAOYSA-N nitrilotriacetic acid Chemical class OC(=O)CN(CC(O)=O)CC(O)=O MGFYIUFZLHCRTH-UHFFFAOYSA-N 0.000 description 1
- 230000003287 optical effect Effects 0.000 description 1
- 239000003960 organic solvent Substances 0.000 description 1
- 125000004430 oxygen atom Chemical group O* 0.000 description 1
- 239000000843 powder Substances 0.000 description 1
- 230000002265 prevention Effects 0.000 description 1
- 150000003138 primary alcohols Chemical class 0.000 description 1
- 239000010453 quartz Substances 0.000 description 1
- 238000000926 separation method Methods 0.000 description 1
- 238000010008 shearing Methods 0.000 description 1
- 229910000030 sodium bicarbonate Inorganic materials 0.000 description 1
- 235000017557 sodium bicarbonate Nutrition 0.000 description 1
- UIIMBOGNXHQVGW-UHFFFAOYSA-M sodium bicarbonate Substances [Na+].OC([O-])=O UIIMBOGNXHQVGW-UHFFFAOYSA-M 0.000 description 1
- 159000000000 sodium salts Chemical class 0.000 description 1
- 239000002195 soluble material Substances 0.000 description 1
- 125000001424 substituent group Chemical group 0.000 description 1
- 238000006467 substitution reaction Methods 0.000 description 1
- BDHFUVZGWQCTTF-UHFFFAOYSA-M sulfonate Chemical compound [O-]S(=O)=O BDHFUVZGWQCTTF-UHFFFAOYSA-M 0.000 description 1
- 150000003467 sulfuric acid derivatives Chemical class 0.000 description 1
- VZCYOOQTPOCHFL-UHFFFAOYSA-N trans-butenedioic acid Natural products OC(=O)C=CC(O)=O VZCYOOQTPOCHFL-UHFFFAOYSA-N 0.000 description 1
- 238000012546 transfer Methods 0.000 description 1
- 238000009834 vaporization Methods 0.000 description 1
- 230000008016 vaporization Effects 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
- C11D3/20—Organic compounds containing oxygen
- C11D3/22—Carbohydrates or derivatives thereof
- C11D3/221—Mono, di- or trisaccharides or derivatives thereof
-
- 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
- C11D1/66—Non-ionic compounds
- C11D1/662—Carbohydrates or derivatives
-
- 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
Definitions
- the invention relates to preparation of aqueous detergent slurries with reduced viscosity. This invention also relates to preparation of " a particulate detergent and the novel detergent composition.
- Particulate detergent compositions are generally prepared by forming an aqueous slurry of the materials which form the deter ⁇ gent and drying the slurry.
- the slurry of the detergent forming composition is generally formed in a apparatus called a crutcher. Since the water present 1n the slurry must be removed to form a particulate detergent, the slurry generally has as low a con ⁇ centration of water as permitted by the required handling of the slurry in the drying operation.
- Detergent compositions generally comprise at least one sur- factant, detergent builders such as phosphates, maleic acid/vinyl ether copolymers, silicates, carbonates, salts of nitrilotriacetic acid, zeolites and the like, fillers such as sodium sulfate, sodium chloride and various additives which prevent redeposition, brighten the clothes, chelate metal ions and the like.
- detergent builders such as phosphates, maleic acid/vinyl ether copolymers, silicates, carbonates, salts of nitrilotriacetic acid, zeolites and the like
- fillers such as sodium sulfate, sodium chloride and various additives which prevent redeposition, brighten the clothes, chelate metal ions and the like.
- patent 4,536,319 which is incorporated herein by reference discloses detergent compositions containing alkyl polyglycoside surfactant and a co-surfactant.
- alkyl polyglycoside surfactant and a co-surfactant.
- One of the detergent builders which has been substituted for the now banned phosphates is sodium carbonate.
- the inclusion of alkyl polyglycosides alone in a carbonate built detergent composition does not have the effect of substantially reducing the viscosity of the slurry. Accordingly, slurries containing higher propor ⁇ tions of water are required so that the detergent slurry can be handled and transported to the drying apparatus. The inclusion of the additional water in the detergent slurry reduces the capacity of the drying apparatus and increases the cost of preparing the particulate detergent composition.
- the viscosity of a carbonate containing and particularly a carbonate built detergent slurry can be substantially reduced by including in the detergent slurry composition a viscosity reducing amount of an alkyl polyglycoside and an alkali metal chloride.
- the viscosity of a detergent slurry containing a zeolite can also be reduced by addi ⁇ tion of alkyl polyglycoside and an alkali metal chloride to the detergent slurry.
- the process for preparing a particulate detergent composition of the present invention comprises forming an aqueous slurry com- prising per 100 parts of total slurry weight:
- the non-aqueous composition comprises: a. from about 2% to 50% by weight of an anionic surfac- tant, a nonionic surfactant or mixture thereof; b. from about 10% to about 70% by weight of an alkali metal carbonate builder; c. from about 0 to about 50% by weight of at least one supplemental builder; d. from about 0 to about 60% by weight of at least one filler; e. from about 0 to about 15% by weight of at least one additive; f. at least a viscosity reducing amount of at least one alkyl glycoside and an alkali metal chloride;
- the invention also includes a slurry having the above com ⁇ position and a particulate detergent formed from the dried slurry.
- the slurry is preferably dried by spray drying.
- Fig. 1 is a bar graph illustrating a comparison of the viscosity of carbonate built detergent slurries containing alkali metal chlorides, alkyl polyglycoside and a mixture of alkali metal chloride and alkyl polyglucoside.
- Fig. 2 1s a bar graph illustrating the effect of alkali metal chloride and alkyl polyglucosides of varying compositions on the viscosity of a carbonate built detergent slurry.
- Fig. 3 is bar graph illustrating the effectiveness of alkali metal chloride and alkyl polyglucoside on the viscosity of a car ⁇ bonate built detergent slurry containing an anionic and nonionic surfactant.
- Fig. 4 is a bar graph illustrating the effect of alkali metal chloride and alkyl polyglucoside on the viscosity of a carbonate built detergent slurry containing a nonionic surfactant.
- U.S. Patent 4,675,127 discloses that the addition of alkyl polyglycoside to a detergent slurry containing a phosphate builder substantially reduces the viscosity of the slurry.
- the amount of water in the slurry can be reduced to form a slurry with a higher concentration of active ingredients having a viscosity which still permits handling of the detergent slurry with normal handling equipment. That is, the addition of more non-aqueous materials to the alkyl polyglycoside containing slurry produces a slurry with a viscosity and pu pability not higher than a slurry of lower con- centration not containing the alkyl polyglycoside.
- alkyl polyglucoside alone does not substantially reduce the viscosity of carbonate containing detergent slurries.
- Applicants have unexpectedly discovered that the combination of alkyl glycoside and particularly an alkyl polyglycoside and an alkali metal chloride substantially reduces the viscosity of car ⁇ bonate containing and particularly carbonate built detergent slurries.
- the discovery is unexpected since the addition of either alkyl glycoside or an alkali metal chloride salt alone to a carbonate containing detergent slurry does not substantially reduce the viscosity of the slurry and, in some cases, actually increases the viscosity.
- the phrase "carbonate built" detergent slurry refers to a slurry wherein a major portion of the builder 1s an alkali metal carbonate, bicarbonate, sesquicarbonate or mix ⁇ ture thereof.
- the Inclusion of alkyl glycoside and the alkali metal chloride in the carbonate built or carbonate containing detergent slurry also stabilizes the slurry so that the viscosity of the slurry does not substantially increase over the period of time between the detergent slurry preparation and transfer to the drying apparatus.
- the viscosity of a detergent slurry increases as the detergent slurry ages. This is particularly cri ⁇ tical in low water slurries. Low water slurries as they age and the ingredients hydrate- tend to become granular and can set up as a solid material.
- the addition of alkyl glycoside and alkali metal chloride to the detergent slurries of the invention permits the slurry to remain fluid over long periods of time. Even when the viscosity of the carbonate containing slurry does not require reduction, the addition of alkyl glycoside and preferably alkyl polyglycoside and alkali metal chloride improves the texture and handleability of the slurry.
- the present invention precludes such an occurrence.
- the present invention can be practiced as an emergency measure wherein a mixture of alkyl glycoside and alkali metal chloride can be introduced into the slurry and mixed therewith to pre ⁇ vent the slurry from setting-up during a plant emergency.
- the addition of alkyl glycoside and the alkali metal chloride to a detergent composition containing a nonionic surfactant can aid in homogenizing the slurry and preventing separating out or oiling out of the nonionic surfactant.
- detergent slurries are prepared at an elevated temperature 1n a range of about 130 to about 175°F.
- the solubility of nonionic surfactants generally decreases as the temperature Increases.
- the nonionic surfac ⁇ tants if present in substantial quantities, tend to separate from the detergent slurry and form a discontinuous or oily phase.
- the 5 addition of alkyl glycoside and the alkali metal chloride aid in dispersing the nonionic surfactant throughout the detergent slurry.
- the non-aqueous portion of the detergent slurry of the pre ⁇ sent invention comprises from 2 to 50% by weight of an anionic
- the surfactant is present at from about 8 to about 25% by weight and more preferably from about 10 to 20% by weight.
- the detergent slurry comprises an anionic surfactant or a mixture of an anionic surfactant and nonionic . surfactant in a
- L5. ratio of from 5:1 to about 1:2 on a weight basis.
- Typical anionic surfactants which can be included in the com ⁇ position of the present invention include linear or branched alkyl- aryl sulfonates or derivatives thereof (alkylbenzenesulfonate, alkyltoluenesulfonate, alkylphenolsulfonates and the like).
- alkali metal salts of fatty acids commonly referred to as "soaps”
- alcohol sulfates alcohol ether sulfates; alkane sulfonates; alkene sulfonates; alpha sulfo methyl fatty esters; and the like.
- Anionic surfactants are well known in the art.
- the preferred anionic surfactants are alkyl aryl sulfonate salts.
- nonionic surfactants useful in the composition of the present invention include alkoxylated (especially ethoxylated and mixed ethoxylated, propoxylated adducts of primary or secondary fatty (C8-C20) alcohols, alkoxylated al ylphenols, fatty alkanola- ides, and the like.
- alkoxylated especially ethoxylated and mixed ethoxylated, propoxylated adducts of primary or secondary fatty (C8-C20) alcohols, alkoxylated al ylphenols, fatty alkanola- ides, and the like.
- Nonionic surfactants are well known in the
- the alkali metal carbonates are present 1n the non-aqueous portion of the composition at from about 15 to about 70% by weight and preferably from about 30 to about 60% by weight and more preferably from about 40 to about 55% by weight.
- the alkali metal carbonates act as detergent builders.
- the alkali metal carbonate is sodium carbonate.
- the phrase carbonate as used herein encompasses alkali metal carbonate, bicarbonate, and sesquicarbonate preferably the carbonate is sodium carbonate or bicarbonate.
- the non-aqueous portion of the detergent composition of the present invention can also contain additional builders which include the known builder materials conventionally employed in the manufacture of powder or granular detergent products.
- builder ingredients include alkali metal citrates, alkali metal silicates, alkali metal nitrilotriacetates, carboxymethyl- oxy-succinates, zeolites and the like.
- additional builders are present at from 15-40% by weight.
- the composition of the present invention can contain minor amounts of phosphate builders. However, inclusion of more than 20% by weight of the non-aqueous portion of the composition of a phosphate builder can unduly increase the viscosity of the slurry.
- the present inven ⁇ tion is useful for reducing the viscosity of slurries containing a major portion of a zeolite builder containing a carbonate builder.
- the detergent slurry of the present invention can con ⁇ tain filler materials.
- Filler materials are generally water- soluble materials which do not adversely affect the detergent properties of the mixture.
- Filler materials are generally neutral water soluble compositions such as sodium sulfate and sodium chloride.
- Fillers can be present up to 60% by weight of the non- aqueous portion of the detergent composition. Preferably the fillers are present at from 15 to 35% by weight and most pre ⁇ ferably from 20 to 30% by weight of the non-aqueous portion of the detergent composition.
- the filler materials are well known in the art. Sodium sulfate is a well known filler.
- the detergent composition can contain up to 20% by weight of at least one additive.
- Additives are materials such as antl- redepositlon agents, fragrances, chelating agents, complexing agents, colorants, foam stabilizers, organic solvents, whitening agents, brightening agents and the like.
- Preferably additives are present at from 0.5 to about 5%.
- the additive compositions useful in detergent formulations are well known to those skilled in the art and will not be set out in detail in this application.
- composition of the present invention must contain at least a viscosity reducing amount of an alkylglycoside and an alkali metal chloride. Generally, from about 0.5 to about 10% by weight of the alkylglycoside is sufficient to reduce the viscosity of the detergent slurry composition when used with from about
- alkali metal chloride 0.5 to about 10% by weight of an alkali metal chloride. Both the alkylglycoside and the alkali metal chloride must be present to achieve the substantial viscosity reducing effects in the detergent slurry composition of the present invention.
- the alkylglycoside surfactants suitable for use in the prac ⁇ tice of the present invention include glycosides of the formula: RO-CRiOJy- GJxZb wherein R is a monovalent organic radical containing from about 6 to about 30 (preferably from about 8 to about 18) carbon atoms; R 1 is a divalent hydrocarbon radical containing from about 2 to about 4 carbon atoms; 0 1s an oxygen atom; y is a number which has an average value from about 0 to about 1 and is preferably 0; G is a moiety derived from a reducing saccharide containing 5 or 6 carbon atoms; and x is a number having an average value from about 1 to 5 (prefer ⁇ ably from 1.1 to 2).
- Z is 0 2 M, 0 C-R2 0(CH 2 ) p C0 2 M, OSO3M, 0(CH 2 )pS0 3 M;
- Z can be 0 2 M only if Z is in place of a primary hydroxyl group 1n which the primary hydroxyl -bearing
- Alkyl glycosides containing Z substituents and their method of preparation are disclosed in United States Application Serial No. 86,990 filed August 19, 1987, which is incorporated herein by reference.
- R is generally the residue of a fatty alcohol having from about 8-30 and preferably 8-18 carbon atoms.
- glycoside surfactants for use in the practice of the invention include alkylpolyglycoside compositions in which R is a monovalent aliphatic radical (linear or branched) containing from 8 to 18 carbon atoms; y is zero; G is a glucose moiety or a moiety derived therefrom; x is a number having an average value of from about 1.0 to about 2.0.
- the alkylpolyglycosides can contain a glycosal moiety which is selected from group consisting of fructose, glucose, anose, galactose, talose, gulose, allose, altose, itose, aribanose, xylose, luxose, ribose and mixtures thereof.
- a glycosal moiety which is selected from group consisting of fructose, glucose, anose, galactose, talose, gulose, allose, altose, itose, aribanose, xylose, luxose, ribose and mixtures thereof.
- the glyco ⁇ sal moiety is a glucose moiety.
- a viscosity reducing amount of the alkylglycoside generally ranges from 0.5 to 10% by weight of the non-aqueous portion of the detergent composition.
- detergent compositions containing more than 10% of the alkylglycoside are also encompassed within the present invention.
- the alkylglycoside is a surfactant per se and can be utilized in higher amounts.
- suitable viscosity reduction can generally be obtained in the range from about 0.5 to about 8% by weight.
- the alkylglycoside is an alkyl polyglycoside and most preferably an alkyl polyglucoside.
- the alkali metal chloride salts when used with the alkylgly- cosides in the practice of the present invention substantially reduce the viscosity of the aqueous detergent slurry composition of the present invention.
- the alkali metal chlorides are present in from about 0.5 to about 10% by weight of the com ⁇ position. Greater amounts of alkali metal chloride can be present in the composition.
- the alkali metal chloride is sodium chloride, potassium chloride or mixtures thereof.
- the alkylglycoside and the alkali metal chloride salt in the detergent composition can reduce the water content of the slurry up to 30% or more without a significant increase in the viscosity of the slurry.
- Reduction in the water content of the slurry results in a conco - itta ⁇ t increase in the throughput of the drying apparatus since a substantial portion of the thermal load of a drying apparatus is utilized to provide the latent heat of vaporization for the water which is removed from the detergent slurry to form the particulate detergent composition.
- the preferred method of drying is spray drying which is well known in the art and will not be further described here.
- the higher solids content also tends to produce a dried detergent having a higher bulk density.
- the higher bulk density permits packaging the detergent in smaller packages and, there ⁇ fore, reduces packaging and shipping costs.
- the discovery of the present invention is unexpected since neither the alkylglycoside nor the alkali metal chloride alone have a substantial viscosity reducing effect on the detergent slurry of the invention. Only the combination of the alkylglycoside and the alkali metal chloride substantially reduces the viscosity of the detergent slurry composition.
- the detergent slurry compositions with the reduced viscosity are prepared by adding the surfactants, the alkylglycoside, the alkali metal chloride and any other liquid or minor amounts of dry ingredients to the water for forming the slurry.
- the water con ⁇ taining the materials is agitated, and the dry ingredients which are to be added in major proportions are mixed with the aqueous portion. It takes a short period of mixing, generally from 5 to 25 minutes, to form a slurry with a generally stable viscosity.
- the viscosity of the detergent slurry can vary.
- the slurries were prepared in a 600 ml tall form beaker using 420 to 470 g of non-aqueous ingredi ⁇ ents.
- a LIGHTNIN® mixer having a single, three blade stirrer (2 inches in diameter) positioned one half inch from the bottom of the beaker was used for mixing.
- the mixer was attached to a Variac® power control unit so that the mixing could be done at the highest possible speed without entraining air into the slurry. Air causes the slurry viscosity to increase.
- the beaker was placed in a constant temperature water cir- culating bath maintained at 160°F. Water was introduced into the beaker, and the surfactants, silicates, alkyl glycosides and alkali metal chloride along with any additives were mixed with the water. The sodium carbonate and any other builders and fillers were then added to the aqueous mixture in the beaker over a 10 minute period. The maximum mixing speed was attained before all the ingredients were added. The maximum mixer speed was about 2000 rpm as measured by a strobe light.
- the stirring at the maximum mixing speed was continued for 5 minutes after all dry ingredients had been added.
- the viscosity was measured after the slurry had set for 10 minutes.
- the slurry was then mixed for an additional 20 minutes, and a second visco ⁇ sity taken.
- Some slurries were mixed for a second 20 minute period and some were permitted to sit for 16 hours at 160°F, then stirred and the viscosity measured. Since the viscosity was relatively stable and did not change significantly after the first 20 minute mixing period, the viscosities reported are shown as the 5 minute and the 25 minute mixing periods.
- the viscosities of the slurry were measured by an RVT model viscosimeter mounted on a Brookfield Helipath Stand.
- the Brookfield Helipath Stand slowly lowers the viscosimeter into the slurry so that the rotating shearing spindle describes a helical path through the test sample.
- the readings were taken in the bot ⁇ tom half of the slurry to minimize the effect of mixture lost or crust formation on the top of the slurry. A minimum of ten readings were taken on average to get a representative viscosity.
- the experiment reported in Fig. 1 was done to determine the effect of sodium chloride, potassium chloride, alkyl polyglu ⁇ coside and a mixture of alkyl polyglucoside and sodium chloride and alkyl polyglucoside and potassium chloride on the viscosity of a slurry.
- the slurry was prepared utilizing an anionic surfactant and sodium carbonate.
- the slurry contained 28% water and 72% by weight of the following compositions:
- NaLAS dodecylbenzene sulfonate sodium salt sold under the Tradename C-560 Slurry from Vista Chemical Company.
- APG® 500 1s an alkylpolyglucoside with a 12-13 carbon alkyl group and degree of polymerization (DP) of less than 1.4.
- Sodium Silicate was 47% solids with a 1:2.4 Na 2 0/Si0 2 ratio sold under Tradename RU® from Philadelphia Quartz Corporation. The sodium silicate was used 1n all of the examples.
- a slurry was prepared first with no additives having the com ⁇ position shown under Control.
- a second slurry was prepared substituting 5% of sodium chloride for 5% of the sodium sulfate in the formulation.
- a second formulation wherein 5% of potassium chloride was substituted for 5% of the sodium sulfate in the for ⁇ mulation.
- a fourth formulation was prepared in which 2% APG® 500 was substituted for 2% of the sodium sulfate in the formulation.
- a fifth formulation was prepared in which 2% APG® 500 and 5% sodium chloride were substituted for 7% of the sodium sulfate in the composition.
- a sixth formulation was prepared wherein 2% APG® and 5% potassium chloride was substituted for 7% of the sodium sulfate.
- slurries were prepared to determine the effect of alkyl chain length and degree of polymerization (DP) on the viscosity of a anionic detergent, carbonate built system con- taining 28% water.
- the slurry is noted as containing 72% solids by weight. The solids are the portion which remains after removal of water. Not all of the materials are necessarily solids but can be viscous liquids.
- the slurries were prepared as described above and the visco- sities measured after 25 minutes of stirring at 2000 rpm.
- the alkyl polyglycoside was of the formula RO-(R 1 0-) y G x wherein y was equal to 0, Z was a glucose residue and x is the degree of polymerization and R is an alkyl group having from 8 to 13 carbon atoms.
- Fig. 2 clearly shows that alkyl polyglucosides, over a broad composition range, when combined with an alkali metal chloride reduces the viscosity of a carbonate built detergent system.
- the example was carried out to show the reduction in visco ⁇ sity of an anionic/nonionic surfactant carbonate built detergent system by the incorporation therein of the APG ® alkyl polygluco ⁇ side and an alkali metal chloride.
- a control formulation and an equivalent formulation containing APG® were prepared.
- the for ⁇ mulations were as follows:
- Fig. 3 shows the viscosity of the control slurry containing 37.5% water and an APG and alkali metal chloride containing slurry containing 26% water. Even though the slurry containing APG ® and alkali metal chloride contained only 69% of the water in the control slurry, the visco- was only about 1/6 as high.
- the values for the viscosities shown in the bar graph were as follows:
- a slurry containing a substantially higher percentage of nonaqueous material could be processed with an increase in the efficiency of the drying apparatus.
- the lower viscosity would be advantageous in a spray drying process.
- the APG ® in the formulation aids in preventing the oiling out of the nonionic detergent.
- NaLAS sodium dodecylbe ⁇ zene sulfonate.
- LAE 25-7 is an ethoxylated primary alcohol nonionic surfac ⁇ tant sold under Trademark Neodol 25-7 from Shell Chemical Company.
- Example 4 The example illustrates the effect of APG® and potassium chloride on the viscosity of a nonionic surfactant, carbonate built detergent system.
- the detergent slurries were prepared and visco ⁇ sities determined as described above.
- the results of the experi ⁇ ment are set forth in Fig. 4.
- the figure clearly shows that the combination of APG® and potassium chloride has a substantial effect on the viscosity of the aqueous detergent slurry.
- APG ® surfactant added to the nonionic detergent slurry composition helps in preventing the nonionic detergent from oiling out or separating from the slurry at the elevated tem ⁇ perature (160°F) used for preparing these slurries.
- the formulation utilized was as follows: Control APG
- APG® 225 refers to an alkylpolyglucoside with a 9-11 carbon alkyl group and x is 1.5-1.6.
- the other APG® materials were as set forth in example 2.
- Anionic Surfactant (dodecylbenzenesulfonate sodium salt) 15
- the effect of APG® and alkali metal chloride on the viscosity of slurries containing an anionic and nonionic surfactant and sodium carbonate was determined by preparing six slurries having a non-aqueous content of from 60.5 to 74%. Potassium chloride and APG® were added to these slurries and the viscosity of the slurries determined. The slurries were prepared according to the method set forth above. The composition of the slurry (dry solid) is shown in Table II. The results of the experiment are set forth in Table II. It can be seen from Table II that potassium chloride alone has a detrimental effect on the viscosity of the detergent slurry.
- Potassium chloride alone without APG® increased the viscosity of the slurry.
- the APG prevented oiling-out of the nonionic surfactant from the slurry composition.
- the prevention of the separation of nonionic surfactant from the detergent slurry is a valuable attribute of incorporation of the APG into the slurry composition.
- Anionic Surfactant (dodecylbenzenesulfonate) 12 sodium salt
- Nonionic Surfacant (Neodol 25-7) 12
- Typical detergent formulations which aqueous slurrys can be improved by the addition of small amounts of an alkali metal chloride and an APG® are as follows: Anionic surfactant 5-30% by weight Sodium carbonate 15-70% by weight Sodium sulfate 0-60% by weight Sodium chloride 0-25% by weight Sodium silicate 3-25% by weight Alkyl polyglucosides 0.5-10% by weight
- Anionic surfactant-nonionlc surfactant containing for- mulations are becoming more popular due to the attractive proper ⁇ ties of the anionic and nonionic surfactants when they are combined in a detergent.
- a detergent containing an anionic and a nonionic surfactant would be shown above with the addition of from about 3-15% of the nonionic surfactant. If an all- nonionic surfactant detergent is desired, the anionic surfactant can be replaced in the above formulation by about 3-15% of a nonionic surfactant.
- the addition of APG® and an alkali metal chloride to the composition if the composition does not already contain an alkali metal chloride will substantially reduce the viscosity of an aqueous slurry of the detergent.
- a typical anionic-nonionic formulation would be as follows:
- XP8E-A96 APG ® 500 made with C12-C13 alcohol (Neodol 23) and has an average DP of 1.3 - 1.4
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Abstract
The invention is a process for preparing a carbonate containing detergent slurry with reduced viscosity by incorporating in the detergent slurry from 0.5 to 10 % of an alkylpolyglycoside and 0.5 to 10 % of an alkali metal chloride, the percentage being by weight of the non-aqueous portion of the slurry.
Description
A PROCESS FOR PREPARING A DETERGENT SLURRY AND PARTICULATE DETERGENT COMPOSITION
BACKGROUND OF THE INVENTION
1. Field of the Invention
The invention relates to preparation of aqueous detergent slurries with reduced viscosity. This invention also relates to preparation of" a particulate detergent and the novel detergent composition.
Particulate detergent compositions are generally prepared by forming an aqueous slurry of the materials which form the deter¬ gent and drying the slurry. The slurry of the detergent forming composition is generally formed in a apparatus called a crutcher. Since the water present 1n the slurry must be removed to form a particulate detergent, the slurry generally has as low a con¬ centration of water as permitted by the required handling of the slurry in the drying operation.
Detergent compositions generally comprise at least one sur- factant, detergent builders such as phosphates, maleic acid/vinyl ether copolymers, silicates, carbonates, salts of nitrilotriacetic acid, zeolites and the like, fillers such as sodium sulfate, sodium chloride and various additives which prevent redeposition,
brighten the clothes, chelate metal ions and the like. 2. Statement of Related Art
It is known that the inclusion of a small amount of alkyl glycosides and particularly alkyl polyglycosides in phosphate built detergent slurry compositions, reduces the slurry viscosity so that a higher concentration of the non-aqueuous ingredients can be included in the slurry. U.S. Patent 4,675,127, which is incor¬ porated herein by reference, discloses phosphate built detergent compositions containing small amounts of alkyl polyglycosides to reduce the viscosity of the slurry and permit inclusion of a higher concentration of the non-aqueous ingredients in the slurry. U.S. patent 4,536,319 which is incorporated herein by reference discloses detergent compositions containing alkyl polyglycoside surfactant and a co-surfactant. With the advent of environmental concerns, many locals have banned the use of phosphates in detergent compositions or severely limited the amount of phosphate which can be present. One of the detergent builders which has been substituted for the now banned phosphates is sodium carbonate. The inclusion of alkyl polyglycosides alone in a carbonate built detergent composition, does not have the effect of substantially reducing the viscosity of the slurry. Accordingly, slurries containing higher propor¬ tions of water are required so that the detergent slurry can be handled and transported to the drying apparatus. The inclusion of the additional water in the detergent slurry reduces the capacity of the drying apparatus and increases the cost of preparing the particulate detergent composition.
BRIEF DESCRIPTION OF THE INVENTION Other than in the operating examples, or where otherwise indicated, all numbers expressing quantities of ingredients or reaction conditions used herein are to be understood as modified in all instances by the term "about".
It is been unexpectedly discovered that the viscosity of a
carbonate containing and particularly a carbonate built detergent slurry can be substantially reduced by including in the detergent slurry composition a viscosity reducing amount of an alkyl polyglycoside and an alkali metal chloride. The viscosity of a detergent slurry containing a zeolite can also be reduced by addi¬ tion of alkyl polyglycoside and an alkali metal chloride to the detergent slurry.
The process for preparing a particulate detergent composition of the present invention comprises forming an aqueous slurry com- prising per 100 parts of total slurry weight:
1) from 15 to 50 parts by weight of water; and
2) from 50 to 85 parts by weight of a non-aqueous com¬ position, the non-aqueous composition comprises: a. from about 2% to 50% by weight of an anionic surfac- tant, a nonionic surfactant or mixture thereof; b. from about 10% to about 70% by weight of an alkali metal carbonate builder; c. from about 0 to about 50% by weight of at least one supplemental builder; d. from about 0 to about 60% by weight of at least one filler; e. from about 0 to about 15% by weight of at least one additive; f. at least a viscosity reducing amount of at least one alkyl glycoside and an alkali metal chloride;
B. drying the slurry to form the particulate detergent composition. The invention also includes a slurry having the above com¬ position and a particulate detergent formed from the dried slurry. The slurry is preferably dried by spray drying.
Brief Description of the Drawings
Fig. 1 is a bar graph illustrating a comparison of the viscosity of carbonate built detergent slurries containing alkali metal chlorides, alkyl polyglycoside and a mixture of alkali metal chloride and alkyl polyglucoside.
Fig. 2 1s a bar graph illustrating the effect of alkali metal chloride and alkyl polyglucosides of varying compositions on the viscosity of a carbonate built detergent slurry.
Fig. 3 is bar graph illustrating the effectiveness of alkali metal chloride and alkyl polyglucoside on the viscosity of a car¬ bonate built detergent slurry containing an anionic and nonionic surfactant.
Fig. 4 is a bar graph illustrating the effect of alkali metal chloride and alkyl polyglucoside on the viscosity of a carbonate built detergent slurry containing a nonionic surfactant.
DETAILED DESCRIPTION OF THE INVENTION All percentages shown are by weight unless otherwise noted.
U.S. Patent 4,675,127 discloses that the addition of alkyl polyglycoside to a detergent slurry containing a phosphate builder substantially reduces the viscosity of the slurry. The amount of water in the slurry can be reduced to form a slurry with a higher concentration of active ingredients having a viscosity which still permits handling of the detergent slurry with normal handling equipment. That is, the addition of more non-aqueous materials to the alkyl polyglycoside containing slurry produces a slurry with a viscosity and pu pability not higher than a slurry of lower con- centration not containing the alkyl polyglycoside. However, alkyl polyglucoside alone does not substantially reduce the viscosity of carbonate containing detergent slurries.
Applicants have unexpectedly discovered that the combination of alkyl glycoside and particularly an alkyl polyglycoside and an alkali metal chloride substantially reduces the viscosity of car¬ bonate containing and particularly carbonate built detergent slurries. The discovery is unexpected since the addition of either alkyl glycoside or an alkali metal chloride salt alone to a carbonate containing detergent slurry does not substantially reduce the viscosity of the slurry and, in some cases, actually increases the viscosity. The phrase "carbonate built" detergent
slurry refers to a slurry wherein a major portion of the builder 1s an alkali metal carbonate, bicarbonate, sesquicarbonate or mix¬ ture thereof. A carbonate containing detergent slurry 1s one 1n which the alkali metal carbonate, bicarbonate or sesquicarbonate 1s present but does not comprise more than 50% of the builder.
The Inclusion of alkyl glycoside and the alkali metal chloride in the carbonate built or carbonate containing detergent slurry also stabilizes the slurry so that the viscosity of the slurry does not substantially increase over the period of time between the detergent slurry preparation and transfer to the drying apparatus. Generally, the viscosity of a detergent slurry increases as the detergent slurry ages. This is particularly cri¬ tical in low water slurries. Low water slurries as they age and the ingredients hydrate- tend to become granular and can set up as a solid material. The addition of alkyl glycoside and alkali metal chloride to the detergent slurries of the invention permits the slurry to remain fluid over long periods of time. Even when the viscosity of the carbonate containing slurry does not require reduction, the addition of alkyl glycoside and preferably alkyl polyglycoside and alkali metal chloride improves the texture and handleability of the slurry.
In the past, when it was necessary to hold the slurry in the crutcher due to malfunctioning of plant equipment, the slurry had to be diluted to prevent setting-up of the slurry as a solid material. The present invention precludes such an occurrence. The present invention can be practiced as an emergency measure wherein a mixture of alkyl glycoside and alkali metal chloride can be introduced into the slurry and mixed therewith to pre¬ vent the slurry from setting-up during a plant emergency. The addition of alkyl glycoside and the alkali metal chloride to a detergent composition containing a nonionic surfactant can aid in homogenizing the slurry and preventing separating out or oiling out of the nonionic surfactant. Generally, detergent slurries are prepared at an elevated temperature 1n a range of about 130 to about 175°F. The solubility of nonionic surfactants
generally decreases as the temperature Increases. At the detergent slurry preparation temperature, the nonionic surfac¬ tants, if present in substantial quantities, tend to separate from the detergent slurry and form a discontinuous or oily phase. The 5 addition of alkyl glycoside and the alkali metal chloride aid in dispersing the nonionic surfactant throughout the detergent slurry.
The non-aqueous portion of the detergent slurry of the pre¬ sent invention comprises from 2 to 50% by weight of an anionic
10" surfactant, a nonionic surfactant or a mixture thereof. Prefer¬ ably, the surfactant is present at from about 8 to about 25% by weight and more preferably from about 10 to 20% by weight. Prefer¬ ably, the detergent slurry comprises an anionic surfactant or a mixture of an anionic surfactant and nonionic. surfactant in a
L5. ratio of from 5:1 to about 1:2 on a weight basis.
Typical anionic surfactants which can be included in the com¬ position of the present invention include linear or branched alkyl- aryl sulfonates or derivatives thereof (alkylbenzenesulfonate, alkyltoluenesulfonate, alkylphenolsulfonates and the like). Metal
20 (especially alkali metal) salts of fatty acids (commonly referred to as "soaps"); alcohol sulfates; alcohol ether sulfates; alkane sulfonates; alkene sulfonates; alpha sulfo methyl fatty esters; and the like. Anionic surfactants are well known in the art. The preferred anionic surfactants are alkyl aryl sulfonate salts.
25- The nonionic surfactants useful in the composition of the present invention Include alkoxylated (especially ethoxylated and mixed ethoxylated, propoxylated adducts of primary or secondary fatty (C8-C20) alcohols, alkoxylated al ylphenols, fatty alkanola- ides, and the like. Nonionic surfactants are well known in the
30 art and a detailed explanation of their structures and use will not be presented here.
Mixtures of anionic and nonionic surfactants are particularly preferred since the detergents containing such mixtures maintain the advantageous and desirable properties of both the anionic and
35 the nonionic surfactants.
The alkali metal carbonates are present 1n the non-aqueous portion of the composition at from about 15 to about 70% by weight and preferably from about 30 to about 60% by weight and more preferably from about 40 to about 55% by weight. The alkali metal carbonates act as detergent builders. Preferably, the alkali metal carbonate is sodium carbonate. The phrase carbonate as used herein encompasses alkali metal carbonate, bicarbonate, and sesquicarbonate preferably the carbonate is sodium carbonate or bicarbonate. The non-aqueous portion of the detergent composition of the present invention can also contain additional builders which include the known builder materials conventionally employed in the manufacture of powder or granular detergent products. Examples of such builder ingredients include alkali metal citrates, alkali metal silicates, alkali metal nitrilotriacetates, carboxymethyl- oxy-succinates, zeolites and the like. Preferably additional builders are present at from 15-40% by weight. The composition of the present invention can contain minor amounts of phosphate builders. However, inclusion of more than 20% by weight of the non-aqueous portion of the composition of a phosphate builder can unduly increase the viscosity of the slurry. The present inven¬ tion is useful for reducing the viscosity of slurries containing a major portion of a zeolite builder containing a carbonate builder. The detergent slurry of the present invention can con¬ tain filler materials. Filler materials are generally water- soluble materials which do not adversely affect the detergent properties of the mixture. Filler materials are generally neutral water soluble compositions such as sodium sulfate and sodium chloride. Fillers can be present up to 60% by weight of the non- aqueous portion of the detergent composition. Preferably the fillers are present at from 15 to 35% by weight and most pre¬ ferably from 20 to 30% by weight of the non-aqueous portion of the detergent composition. The filler materials are well known in the art. Sodium sulfate is a well known filler.
The detergent composition can contain up to 20% by weight of at least one additive. Additives are materials such as antl- redepositlon agents, fragrances, chelating agents, complexing agents, colorants, foam stabilizers, organic solvents, whitening agents, brightening agents and the like. Preferably additives are present at from 0.5 to about 5%. The additive compositions useful in detergent formulations are well known to those skilled in the art and will not be set out in detail in this application.
The composition of the present invention must contain at least a viscosity reducing amount of an alkylglycoside and an alkali metal chloride. Generally, from about 0.5 to about 10% by weight of the alkylglycoside is sufficient to reduce the viscosity of the detergent slurry composition when used with from about
0.5 to about 10% by weight of an alkali metal chloride. Both the alkylglycoside and the alkali metal chloride must be present to achieve the substantial viscosity reducing effects in the detergent slurry composition of the present invention.
The alkylglycoside surfactants suitable for use in the prac¬ tice of the present invention include glycosides of the formula: RO-CRiOJy- GJxZb wherein R is a monovalent organic radical containing from about 6 to about 30 (preferably from about 8 to about 18) carbon atoms; R1 is a divalent hydrocarbon radical containing from about 2 to about 4 carbon atoms; 0 1s an oxygen atom; y is a number which has an average value from about 0 to about 1 and is preferably 0; G is a moiety derived from a reducing saccharide containing 5 or 6 carbon atoms; and x is a number having an average value from about 1 to 5 (prefer¬ ably from 1.1 to 2).
Z is 02M, 0 C-R2 0(CH2)pC02M, OSO3M, 0(CH2)pS03M; R2 is (CH2)2C02M or CH=CHC02M; Z can be 02M only if Z is in place
of a primary hydroxyl group 1n which the primary hydroxyl -bearing
0 P carbon atom, -CH20H 1s oxidized to form a -C-OM group; b is a number of from 1 to 3x+l preferably an average of from 0.5 to 2 per glycosal group; p is 1 to 10.
Alkyl glycosides containing Z substituents and their method of preparation are disclosed in United States Application Serial No. 86,990 filed August 19, 1987, which is incorporated herein by reference.
R is generally the residue of a fatty alcohol having from about 8-30 and preferably 8-18 carbon atoms.
A particularly preferred group of glycoside surfactants for use in the practice of the invention include alkylpolyglycoside compositions in which R is a monovalent aliphatic radical (linear or branched) containing from 8 to 18 carbon atoms; y is zero; G is a glucose moiety or a moiety derived therefrom; x is a number having an average value of from about 1.0 to about 2.0.
The alkylpolyglycosides can contain a glycosal moiety which is selected from group consisting of fructose, glucose, anose, galactose, talose, gulose, allose, altose, itose, aribanose, xylose, luxose, ribose and mixtures thereof. Preferably the glyco¬ sal moiety is a glucose moiety.
A viscosity reducing amount of the alkylglycoside generally ranges from 0.5 to 10% by weight of the non-aqueous portion of the detergent composition. However, detergent compositions containing more than 10% of the alkylglycoside are also encompassed within the present invention. The alkylglycoside is a surfactant per se and can be utilized in higher amounts. However, suitable viscosity reduction can generally be obtained in the range from about 0.5 to about 8% by weight. Preferably the alkylglycoside is an alkyl polyglycoside and most preferably an alkyl polyglucoside.
The alkali metal chloride salts when used with the alkylgly- cosides in the practice of the present invention substantially reduce the viscosity of the aqueous detergent slurry composition
of the present invention. Generally, the alkali metal chlorides are present in from about 0.5 to about 10% by weight of the com¬ position. Greater amounts of alkali metal chloride can be present in the composition. Preferably the alkali metal chloride is sodium chloride, potassium chloride or mixtures thereof.
It has been discovered that inclusion of the alkylglycoside and the alkali metal chloride salt in the detergent composition can reduce the water content of the slurry up to 30% or more without a significant increase in the viscosity of the slurry. Reduction in the water content of the slurry results in a conco - ittaπt increase in the throughput of the drying apparatus since a substantial portion of the thermal load of a drying apparatus is utilized to provide the latent heat of vaporization for the water which is removed from the detergent slurry to form the particulate detergent composition. The preferred method of drying is spray drying which is well known in the art and will not be further described here.
The higher solids content also tends to produce a dried detergent having a higher bulk density. The higher bulk density permits packaging the detergent in smaller packages and, there¬ fore, reduces packaging and shipping costs.
The discovery of the present invention is unexpected since neither the alkylglycoside nor the alkali metal chloride alone have a substantial viscosity reducing effect on the detergent slurry of the invention. Only the combination of the alkylglycoside and the alkali metal chloride substantially reduces the viscosity of the detergent slurry composition.
The detergent slurry compositions with the reduced viscosity are prepared by adding the surfactants, the alkylglycoside, the alkali metal chloride and any other liquid or minor amounts of dry ingredients to the water for forming the slurry. The water con¬ taining the materials is agitated, and the dry ingredients which are to be added in major proportions are mixed with the aqueous portion. It takes a short period of mixing, generally from 5 to 25 minutes, to form a slurry with a generally stable viscosity.
During the Initial mixing period, when the dried Ingredients are being hydrated with the water 1n the mixture, the viscosity of the detergent slurry can vary. After a period of about 25 minutes of mixing the viscosity of the slurry generally stabilizes. At this point, a comparison of viscosities of slurries of substantially the same composition and solid content with and without the alkyl- glycosides and alkali metal chloride, shows that the viscosity of the detergent slurry of the invention is substantially lower than the equivalent slurry not containing the alkylglycoside and the alkali metal chloride.
In the examples which follow, the slurries were prepared in a 600 ml tall form beaker using 420 to 470 g of non-aqueous ingredi¬ ents. A LIGHTNIN® mixer having a single, three blade stirrer (2 inches in diameter) positioned one half inch from the bottom of the beaker was used for mixing. The mixer was attached to a Variac® power control unit so that the mixing could be done at the highest possible speed without entraining air into the slurry. Air causes the slurry viscosity to increase.
The beaker was placed in a constant temperature water cir- culating bath maintained at 160°F. Water was introduced into the beaker, and the surfactants, silicates, alkyl glycosides and alkali metal chloride along with any additives were mixed with the water. The sodium carbonate and any other builders and fillers were then added to the aqueous mixture in the beaker over a 10 minute period. The maximum mixing speed was attained before all the ingredients were added. The maximum mixer speed was about 2000 rpm as measured by a strobe light.
The stirring at the maximum mixing speed was continued for 5 minutes after all dry ingredients had been added. The viscosity was measured after the slurry had set for 10 minutes. The slurry was then mixed for an additional 20 minutes, and a second visco¬ sity taken. Some slurries were mixed for a second 20 minute period and some were permitted to sit for 16 hours at 160°F, then stirred and the viscosity measured. Since the viscosity was relatively stable and did not change significantly after the first 20 minute
mixing period, the viscosities reported are shown as the 5 minute and the 25 minute mixing periods.
The viscosities of the slurry were measured by an RVT model viscosimeter mounted on a Brookfield Helipath Stand. The Brookfield Helipath Stand slowly lowers the viscosimeter into the slurry so that the rotating shearing spindle describes a helical path through the test sample. The readings were taken in the bot¬ tom half of the slurry to minimize the effect of mixture lost or crust formation on the top of the slurry. A minimum of ten readings were taken on average to get a representative viscosity.
The slurry composition and the results of the tests are shown in the examples and the Figures.
EXAMPLES Example 1
The experiment reported in Fig. 1 was done to determine the effect of sodium chloride, potassium chloride, alkyl polyglu¬ coside and a mixture of alkyl polyglucoside and sodium chloride and alkyl polyglucoside and potassium chloride on the viscosity of a slurry. The slurry was prepared utilizing an anionic surfactant and sodium carbonate. The slurry contained 28% water and 72% by weight of the following compositions:
Control APG Percent
15 55 21-16 7
1. NaLAS is dodecylbenzene sulfonate sodium salt sold under the Tradename C-560 Slurry from Vista Chemical Company.
2. APG® 500 1s an alkylpolyglucoside with a 12-13 carbon alkyl group and degree of polymerization (DP) of less than 1.4.
3. Sodium Silicate was 47% solids with a 1:2.4 Na20/Si02 ratio sold under Tradename RU® from Philadelphia Quartz Corporation. The sodium silicate was used 1n all of the examples.
A slurry was prepared first with no additives having the com¬ position shown under Control. A second slurry was prepared substituting 5% of sodium chloride for 5% of the sodium sulfate in the formulation. A second formulation wherein 5% of potassium chloride was substituted for 5% of the sodium sulfate in the for¬ mulation. A fourth formulation was prepared in which 2% APG® 500 was substituted for 2% of the sodium sulfate in the formulation. A fifth formulation was prepared in which 2% APG® 500 and 5% sodium chloride were substituted for 7% of the sodium sulfate in the composition. A sixth formulation was prepared wherein 2% APG® and 5% potassium chloride was substituted for 7% of the sodium sulfate. The slurries contained 28% water and 72% by weight of the formulation. Figure 1 clearly shows the unexpected reduction in the visco¬ sity of the slurry when both APG® 500 and alkali metal chloride were present in the detergent slurry mixture. The results are completely unexpected since neither an alkali metal chloride nor APG® 500 alone substantially affected the viscosity of the detergent slurry.
The values for the viscosities shown on the bar graph of Fig. 1 are as follows:
Viscosity Bar (CPS)
Control 66,200
NaCl 65,000
KC1 61,000 2% APG 62,000
2% APG-5% NaCl 8,000
2% APG-5% KC1 5,000
Example 2
In this example, six slurries were prepared to determine the effect of alkyl chain length and degree of polymerization (DP) on the viscosity of a anionic detergent, carbonate built system con- taining 28% water. The slurry is noted as containing 72% solids by weight. The solids are the portion which remains after removal of water. Not all of the materials are necessarily solids but can be viscous liquids.
The slurries were prepared as described above and the visco- sities measured after 25 minutes of stirring at 2000 rpm.
The alkyl polyglycoside was of the formula RO-(R10-)yGx wherein y was equal to 0, Z was a glucose residue and x is the degree of polymerization and R is an alkyl group having from 8 to 13 carbon atoms.
The results of the experiment are shown in Fig. 2. Fig. 2 clearly shows that alkyl polyglucosides, over a broad composition range, when combined with an alkali metal chloride reduces the viscosity of a carbonate built detergent system.
The value of the viscosities shown on the bar graph were as follows:
Viscosity Bar (CPS)
Control 66,200
KC1 61,000
APG® 225 4,600
APG® 300 4,700 APG® 500 6,400
APG® 550 5,400
Exampl e 3
The example was carried out to show the reduction in visco¬ sity of an anionic/nonionic surfactant carbonate built detergent system by the incorporation therein of the APG® alkyl polygluco¬ side and an alkali metal chloride. A control formulation and an equivalent formulation containing APG® were prepared. The for¬ mulations were as follows:
Control APG™
The formulations were the same except for the substitution of 5% of KCL and 2% APG™ 325 for 7% for the Na2S0 . Fig. 3 shows the viscosity of the control slurry containing 37.5% water and an APG and alkali metal chloride containing slurry containing 26% water. Even though the slurry containing APG® and alkali metal chloride contained only 69% of the water in the control slurry, the visco- was only about 1/6 as high. The values for the viscosities shown in the bar graph were as follows:
Viscosity Bar (CPS)
Control 115,000
APG® 15,500
The example illustrates that in a commercial operation, a slurry containing a substantially higher percentage of nonaqueous material could be processed with an increase in the efficiency of the
drying apparatus. The lower viscosity would be advantageous in a spray drying process. In addition, the APG® in the formulation aids in preventing the oiling out of the nonionic detergent. 1. NaLAS is sodium dodecylbeπzene sulfonate. 2. LAE 25-7 is an ethoxylated primary alcohol nonionic surfac¬ tant sold under Trademark Neodol 25-7 from Shell Chemical Company.
Example 4 The example illustrates the effect of APG® and potassium chloride on the viscosity of a nonionic surfactant, carbonate built detergent system. The detergent slurries were prepared and visco¬ sities determined as described above. The results of the experi¬ ment are set forth in Fig. 4. The figure clearly shows that the combination of APG® and potassium chloride has a substantial effect on the viscosity of the aqueous detergent slurry.
The values for the viscosities shown in the bar graph were as follows:
Bar (CPS) Control 72.5% Solids 13,700
APG® 500 72.5% Solids 8,200
APG® 500 75% Solids 12,100
The addition of the APG® surfactant to the nonionic detergent slurry composition helps in preventing the nonionic detergent from oiling out or separating from the slurry at the elevated tem¬ perature (160°F) used for preparing these slurries. The formulation utilized was as follows: Control APG
In the formulation, a portion of the sodium sulfate was replaced by the APG® and sodium chloride. The amount of sodium sulfate was reduced and the amount of nonaqueous material 1n the slurry remained constant. The example clearly shows that the addition of APG® and an alkali metal chloride substantially redu¬ ces the viscosity of a nonionic carbonate built detergent system. Fig. 4 clearly shows that a detergent slurry with a nonaqueous content of 75%, had a lower viscosity than the control with a nonaqueous portion of the slurry of 72.5% by weight.
Example 5
Twelve slurries were prepared containing different percen¬ tages of nonaqueous ingredients and the viscosity of the slurries determined after five minutes of high shear mixing and after 25 minutes of high shear mixing. The nonaqueous portion of the aqueous detergent slurry is shown in Table I.
The results of the experiments are shown in Table I. APG® 225 refers to an alkylpolyglucoside with a 9-11 carbon alkyl group and x is 1.5-1.6. The other APG® materials were as set forth in example 2.
TABLE I
Effect of APG Surfactants on Viscosity of Slurries Containing Anionic Surfactant and Sodium Carbonate
% Slurry Vi scosi ty (Cps) KCI % APG® Initial* Final**
0 0 0 0
* 5 Min. High Shear Mixing ** 25 Min. High Shear Mixing
Composition of Slurry (Dry Solids Basis)
Raw Material %
Anionic Surfactant (dodecylbenzenesulfonate sodium salt) 15
Sodium Carbonate 55
Sodium Sulfate 16-23
Sodium Silicate 7
Potassium Chloride 0-5
APG® 500 Surfactant 0-2
19
Example 6
The effect of APG® and alkali metal chloride on the viscosity of slurries containing an anionic and nonionic surfactant and sodium carbonate was determined by preparing six slurries having a non-aqueous content of from 60.5 to 74%. Potassium chloride and APG® were added to these slurries and the viscosity of the slurries determined. The slurries were prepared according to the method set forth above. The composition of the slurry (dry solid) is shown in Table II. The results of the experiment are set forth in Table II. It can be seen from Table II that potassium chloride alone has a detrimental effect on the viscosity of the detergent slurry. Potassium chloride alone without APG® increased the viscosity of the slurry. In addition, the APG prevented oiling-out of the nonionic surfactant from the slurry composition. The prevention of the separation of nonionic surfactant from the detergent slurry is a valuable attribute of incorporation of the APG into the slurry composition.
TABLE II
Effect of APG Surfactants on Viscosity of Slurries Containing Anionic and Nonionic Surfactants and Sodium Carbonate
* 5 Min. High Shear Mixing ** 25 Min. High Shear Mixing
Composition of Slurry (Dry Solids Basis)
Raw Material %
Anionic Surfactant (dodecylbenzenesulfonate) 12 sodium salt
Nonionic Surfacant 4
Sodium Carbonate 55
Sodium Sulfate 15-22
Sodium Silicate 7
Potassium Chloride 0-5
APG® Surfactant 0-2
Example 7
The effect of alkali metal chloride and APG® on the viscosity of carbonate built nonionic surfactant detergent slurries is shown in Table III. The composition of the slurries is shown in the Table. The slurries were prepared as described above, and the viscosities measured as described above.
The combination of alkali metal chloride and APG® reduced the viscosity of the slurries.
TABLE III
Effect of APG Surfactants on Viscosity of Slurries Containin
* 5 Min. High Shear Mixing ** 25 Min. High Shear Mixing (1) Nonionic surfactant separated out.
Composition of Slurry (Dry Solids Basis)
Raw Material %
Nonionic Surfacant (Neodol 25-7) 12
Sodium Carbonate 55
Sodium Sulfate 19-26
Sodium Silicate 7
Potassium Chloride 0-5
APG® 500 Surfactant 0-2
Example 8
Slurries were prepared to determine the effect of degree of ethoxylation of the APG polyglucoside on the viscosity of an aqueous detergent slurry. The composition of the slurry is shown in Table IV.
The viscosities of the slurries prepared as described above are set forth in Table IV.
It is clear from Table IV that up to about 1 mol of ethylene oxide per APG® molecule can be used. The examples clearly show that the addition of small amounts of APG® and an alkali metal chloride to a carbonate built aqueous detergent slurry substantially reduces the viscosity of the slurry. The reduction is important since a slurry having a higher concentration of non-aqueous materials can be prepared and dried with a lower input of heat. This permits the capacity of the drier to be increased or the particulate detergent composition to be prepared with a lower imput of energy per unit weight.
The above examples are for illustrative purposes only, and are not intended to limit the scope of the invention. Typical detergent formulations which aqueous slurrys can be improved by the addition of small amounts of an alkali metal chloride and an APG® are as follows: Anionic surfactant 5-30% by weight Sodium carbonate 15-70% by weight Sodium sulfate 0-60% by weight Sodium chloride 0-25% by weight Sodium silicate 3-25% by weight Alkyl polyglucosides 0.5-10% by weight
Anionic surfactant-nonionlc surfactant containing for- mulations are becoming more popular due to the attractive proper¬ ties of the anionic and nonionic surfactants when they are combined in a detergent. A detergent containing an anionic and a nonionic surfactant would be shown above with the addition of from about 3-15% of the nonionic surfactant. If an all- nonionic surfactant detergent is desired, the anionic surfactant
can be replaced in the above formulation by about 3-15% of a nonionic surfactant. The addition of APG® and an alkali metal chloride to the composition, if the composition does not already contain an alkali metal chloride will substantially reduce the viscosity of an aqueous slurry of the detergent.
A typical anionic-nonionic formulation would be as follows:
% Non-Aqueous Component Composition by Weight
Anionic Surfactant 8-15%
Nonionic Surfactant 2-10%
Sodium Carbonate 45-65%
Sodium Silicate 3-10% Soap 0- 5%
Carboxymethyl Cellulose 0.25-1%
(antiredeposition agent)
Optical brightener .25-1.0%
Sodium chloride 2-10% APG® 1-10%
Na2S04 0-30%
TABLE IV
Effect of Ethoxylated APG Surfactants on Viscosity of Slurries Containing Anionic Surfactants and Sodium Carbonate
5 Min. High Shear Mixing ** 25 Min. High Shear Mixing
Composition of Slurry (Dry Solids Basis)
Raw Material %
Anionic Surfacant 15 Sodium Carbonate 55 Sodium Sulfate 16-23 Sodium Silicate 7 Potassium Chloride 0-5 APG® 500 Surfactant 0-3
Example 9
Four sodium carbonate built detergent slurries were prepared containing sodium tripolyphosphate. The slurries were prepared as described above and the viscosities measured as described. The combination of alkali metal chloride and an alkyl polyglucoside were effective in reducing the viscosity of the slurries. The addition of potassium chloride alone substantially increased the viscosity of the slurry.
The results of the experiments are shown in Table V»
TABLE V
Viscosity Reduction of Crutcher Slurries Containing Carbonate, Sulfate and Phosphate
Composition (Dry Solids Basis)
Viscosity (72.5% Solids 100,000 230,000 23,000 30,000 25 Minutes)
Light Density Granular Sodium Tripolyphosphate from FMC Corp.
Example 10
Four slurries were prepared containing a large proportion of zeolite A. Two of the slurries contained sodium tripolyphosphate. All of the slurries contained sodium carbonate. The addition of alkali metal chloride and APG® to the slurries reduced the visco¬ sity of the slurries.
The results of the experiments are shown in Table VI.
TABLE VI
Viscosity Reduction of Crutcher Slurries Containing Carbonates, Sulfates, Zeolites and/or Phosphate
Composition (Dry Solids Basis)
Viscosity (72.5% Solids 47,000 42,000 280,000 82,000 25 Minutes)
Light Density Granular Sodium Tripolyphosphate from FMC Corp.
Example 11
Slurries were prepared utilizing sulfated and carboxylated alkyl polyglucoside derivatives as described above. The viscosi¬ ties were determined as described. The results of the experiments are shown in Table VII. The addition of small amounts of alkali metal chloride and the alkyl polyglucoside to the slurry substantially reduced the viscosity of the slurries.
The invention has been described by way of specific e bodi- ments. The specific embodiments disclosed are not intended to limit the invention.
TABLE VII
Viscosity Reduction of Crutcher Slurries Using APG® Derivatives
Composition (Dry Solids Basis)
% NaLAS
% Na2S04 23 20 20 20 20
% Silicate 7 7 7 7 7
% KCL 0 3 3 3 3
% APG® 83VV-137D* 0 2
26XX-18 2
2VV-88-2 2
XP8E-A96 2
Viscosity (72.5% Solids) 92,000 44,500 31,000 53,000 21,000
*83»V-137D APG® 500 Sulfated with 0.25 equivalent per APG® molecule.
26XX-18 APG® 500 Sulfated with 2.0 equivalent per APG® molecule.
2VV-88-2 APG® 500 Carboxylated with 1.0 equivalent per APG® molecule.
XP8E-A96 APG® 500 made with C12-C13 alcohol (Neodol 23) and has an average DP of 1.3 - 1.4
Claims
1. A process for preparing a particulate detergent composition which comprises:
A. forming an aqueous slurry comprising, per 100 parts per total slurry weight;
1. from about 15 to about 50 parts by weight of water; and
2. from about 50 to about 85 parts by weight of nonaqueous ingredients, the non-aqueous ingredients comprising: a. from about 3 to 50% by weight of an anionic surfactant, nonionic surfactant or mixture thereof; b. from about 10 to about 70% by weight of an alkali metal carbonate builderr c. from about 0 to 50% by weight of at least one supplemental builder; d. from about 0 to about 60% by weight of at least one filler; e. from about 0 to about 15% by weight of at least one addi¬ tive; and f. at least a viscosity reducing amount of an alkyl polyglycoside and an alkali metal chloride;
B. drying the slurry to form the particulate detergent composition.
2. A process of claim 1 wherein the viscosity reducing amount of an alkyl polyglycoside and an alkali metal chloride comprises from about 0.5 to about 10% by weight of an alkyl polyglycoside and from 0.5 to about 10% by weight of at least one alkali metal chloride selected from a group consisting of sodium chloride and potassium chloride.
3. A composition of Claim 1 wherein the non-aqueous ingredients comprise about 8 to about 25 percent by weight of at least one sur¬ factant selected from the group consisting of anionic surfactants and nonionic surfactants; from about 25 to about 60% by weight of sodium carbonate, from about 10 to about 40 percent by weight of at least one
additional builder, from about- 15-35% by weight of sodium sulfate; from about 0.5 to about 5% of additives; from 0.5 to about 10% by weight of an alkyl polyglucoside and from about 0.5 to about 10 per¬ cent by weight of at least one alkali metal chloride selected from the group consisting of sodium chloride and potassium chloride.
4. A process of Claim 1 wherein the alkyl polyglycoside is a composition of the formula:
R0-(Rl0)y(G)xZb
wherein R is a monovalent organic radical containing from about 6 to about 30 carbon atoms;
R1 is a divalent aliphatic hydrocarbon radical containing from 2 to 4 carbon atoms; 0 is oxygen; y is a number which has an average value of 0 to about 1 and is pre¬ ferably 0;
G is moiety derived from a reducing saccharide containing 5 or 6 car¬ bon atoms; x is a number having an average value of from about 1 to about 5;
Z is 02M, 0-C-R2, 0(CH2)pC02M, OSO3M, 0(CH2)pSθ3M wherein R2 is (CH2)2C02M or CH=CHC02M and Z can be 0 M only if Z is in place of a primary hydroxyl group in which the primary hydroxyl-bearing carbon atom, -CH 0H is oxidized to form a
-C-OM group. b is a number from 1 to 3x; and p is 1 to 10.
5. A process of claim 4 wherein the alkyl polyglycoside is an alkyl polyglucoside.
6.,A process of claim 2 wherein the alkyl polyglycoside is an alkyl polyglucoside.
7. The process of claim 1 wherein the slurry is spray dried.
8. A particulate detergent composition which non-aqueous ingredients comprises: a. from about 3 to about 50% by weight of an anionic surfactant, nonionic surfactant and mixtures thereof; b. from about 10 to about 70% by weight of an alkali metal carbonate builder; c. from about 0 to 60% by weight of at least one supplemental builder; d. from about 0 to about 60% by weight of at least one filler; e. from about 0 to about 15% by weight of at least one additive; and f. from about 0.5 to about 25% by weight of an alkyl polyglycoside and from about 0.5 to about 35% by weight of at least one alkali metal chloride.
9. A composition of claim 8 wherein the composition contains from about 0.5 to about 10% by weight of an alkyl polyglycoside and from about 0.5 to about 10% by weight of at least one alkali metal chloride.
10. A detergent composition of claim 8 wherein the alkyl polyglycoside is a composition of the formula:
RO-(RlO)y(G)xZb
wherein R is a monovalent organic radical containing from about 6 to about 30 carbon atoms;
R- is a divalent aliphatic hydrocarbon radical containing from 2 to 4 carbon atoms;
0 1s oxygen; y is a number which has an average value of 0 to about 1 and is pre¬ ferably 0;
G is moiety derived from a reducing saccharide containing 5 or 6 car¬ bon atoms; x is a number having an average value of from about 1 to about 5;
0 Z is 02M, 0-C-R2, 0(CH2)pC0 M, 0S03M, 0(CH2)pS03M wherein R2 is (CH2)2C02M or CH=CHC0 M and Z can be 02M only if Z is in place of a primary hydroxyl group in which the primary hydroxyl-bearing carbon atom, -CH20H is oxidized to form a
-C ϊ-OM group. b is a number from 1 to 3x; and p 'is 1 to 10.
11. A detergent composition of claim 9 wherein the alkyl polyglycoside is an alkyl polyglucoside.
12. A method of claim 1 wherein the supplemental builder comprises a zeolite.
13. A method of claim '1 wherein the supplemental builder comprises not more than about 20% by weight of a phosphate builder.
14. A composition of claim 8 containing a zeolite as a supplemental builder.
15. A composition of claim 8 containing not more than about 20% by weight of a phosphate builder as a supplemental builder.
16. An aqueous slurry comprising from about 15 to about 50 parts by weight of water and from about 50 to about 85 parts by weight of the detergent composition of claim 8.
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
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US26064688A | 1988-10-21 | 1988-10-21 | |
US260,646 | 1988-10-21 |
Publications (1)
Publication Number | Publication Date |
---|---|
WO1990004630A1 true WO1990004630A1 (en) | 1990-05-03 |
Family
ID=22990036
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
PCT/US1989/004603 WO1990004630A1 (en) | 1988-10-21 | 1989-10-19 | A process for preparing a detergent slurry and particulate detergent composition |
Country Status (2)
Country | Link |
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CA (1) | CA2001161A1 (en) |
WO (1) | WO1990004630A1 (en) |
Cited By (11)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
WO1991009932A1 (en) * | 1989-12-12 | 1991-07-11 | Unilever N.V. | Detergent compositions |
WO1992013938A1 (en) * | 1991-01-30 | 1992-08-20 | Henkel Kommanditgesellschaft Auf Aktien | Powdered tenside mixture |
WO1992013936A1 (en) * | 1991-01-30 | 1992-08-20 | Henkel Kommanditgesellschaft Auf Aktien | Low-foam scouring powder |
WO1993011212A1 (en) * | 1991-11-30 | 1993-06-10 | Henkel Kommanditgesellschaft Auf Aktien | Powdery surface-active agent mixture |
WO1993023514A1 (en) * | 1992-05-21 | 1993-11-25 | Henkel Kommanditgesellschaft Auf Aktien | Powdery surfactants mixture |
EP0604996A2 (en) * | 1992-12-31 | 1994-07-06 | Reckitt & Colman Inc. | Hard surface cleaner |
GB2297139A (en) * | 1995-01-17 | 1996-07-24 | Huels Chemische Werke Ag | Use of nonionic surfactants as antifricion agents |
EP0763594A1 (en) | 1995-09-18 | 1997-03-19 | The Procter & Gamble Company | Process for making granular detergents |
WO1999063044A1 (en) * | 1998-06-03 | 1999-12-09 | Henkel Kommanditgesellschaft Auf Aktien | Production of granulates containing alkylpolyglycoside |
US6225272B1 (en) | 1996-11-12 | 2001-05-01 | Henkel Kommanditgesellsehaft Auf Aktien | Dishwashing detergent with enhanced cleaning effect |
WO2002096546A2 (en) * | 2001-05-08 | 2002-12-05 | Cognis Deutschland Gmbh & Co. Kg | Surfactant mixture |
Citations (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US3954679A (en) * | 1973-11-26 | 1976-05-04 | Colgate-Palmolive Company | Viscosity reduction of aqueous alpha-olefin sulfonate detergent composition |
US4675127A (en) * | 1985-09-26 | 1987-06-23 | A. E. Staley Manufacturing Company | Process for preparing particulate detergent compositions |
-
1989
- 1989-10-19 WO PCT/US1989/004603 patent/WO1990004630A1/en unknown
- 1989-10-20 CA CA 2001161 patent/CA2001161A1/en not_active Abandoned
Patent Citations (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US3954679A (en) * | 1973-11-26 | 1976-05-04 | Colgate-Palmolive Company | Viscosity reduction of aqueous alpha-olefin sulfonate detergent composition |
US4675127A (en) * | 1985-09-26 | 1987-06-23 | A. E. Staley Manufacturing Company | Process for preparing particulate detergent compositions |
Cited By (14)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
WO1991009932A1 (en) * | 1989-12-12 | 1991-07-11 | Unilever N.V. | Detergent compositions |
WO1992013938A1 (en) * | 1991-01-30 | 1992-08-20 | Henkel Kommanditgesellschaft Auf Aktien | Powdered tenside mixture |
WO1992013936A1 (en) * | 1991-01-30 | 1992-08-20 | Henkel Kommanditgesellschaft Auf Aktien | Low-foam scouring powder |
US5484548A (en) * | 1991-01-30 | 1996-01-16 | Henkel Kommanditgesellschft Auf Aktien | Low-foam scouring powder |
WO1993011212A1 (en) * | 1991-11-30 | 1993-06-10 | Henkel Kommanditgesellschaft Auf Aktien | Powdery surface-active agent mixture |
WO1993023514A1 (en) * | 1992-05-21 | 1993-11-25 | Henkel Kommanditgesellschaft Auf Aktien | Powdery surfactants mixture |
EP0604996A3 (en) * | 1992-12-31 | 1995-09-27 | Eastman Kodak Co | Hard surface cleaner. |
EP0604996A2 (en) * | 1992-12-31 | 1994-07-06 | Reckitt & Colman Inc. | Hard surface cleaner |
GB2297139A (en) * | 1995-01-17 | 1996-07-24 | Huels Chemische Werke Ag | Use of nonionic surfactants as antifricion agents |
EP0763594A1 (en) | 1995-09-18 | 1997-03-19 | The Procter & Gamble Company | Process for making granular detergents |
US6225272B1 (en) | 1996-11-12 | 2001-05-01 | Henkel Kommanditgesellsehaft Auf Aktien | Dishwashing detergent with enhanced cleaning effect |
WO1999063044A1 (en) * | 1998-06-03 | 1999-12-09 | Henkel Kommanditgesellschaft Auf Aktien | Production of granulates containing alkylpolyglycoside |
WO2002096546A2 (en) * | 2001-05-08 | 2002-12-05 | Cognis Deutschland Gmbh & Co. Kg | Surfactant mixture |
WO2002096546A3 (en) * | 2001-05-08 | 2003-11-13 | Cognis Deutschland Gmbh | Surfactant mixture |
Also Published As
Publication number | Publication date |
---|---|
CA2001161A1 (en) | 1990-04-21 |
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