CN1086538A - Concentrated liquid detergent compositions and methods of making such compositions - Google Patents
Concentrated liquid detergent compositions and methods of making such compositions Download PDFInfo
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- CN1086538A CN1086538A CN 93118314 CN93118314A CN1086538A CN 1086538 A CN1086538 A CN 1086538A CN 93118314 CN93118314 CN 93118314 CN 93118314 A CN93118314 A CN 93118314A CN 1086538 A CN1086538 A CN 1086538A
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- Prior art keywords
- composition
- mixture
- alkyl ether
- earth metal
- carbon atom
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- 239000000203 mixture Substances 0.000 title claims abstract description 75
- 239000007788 liquid Substances 0.000 title claims abstract description 10
- 238000000034 method Methods 0.000 title claims description 26
- 239000003599 detergent Substances 0.000 title claims description 12
- 239000004094 surface-active agent Substances 0.000 claims abstract description 20
- FYYHWMGAXLPEAU-UHFFFAOYSA-N Magnesium Chemical compound [Mg] FYYHWMGAXLPEAU-UHFFFAOYSA-N 0.000 claims abstract description 18
- 239000011777 magnesium Substances 0.000 claims abstract description 18
- 229910052749 magnesium Inorganic materials 0.000 claims abstract description 18
- 239000002253 acid Substances 0.000 claims abstract description 11
- -1 alkyl ether sulfate Chemical class 0.000 claims abstract description 7
- QGZKDVFQNNGYKY-UHFFFAOYSA-O Ammonium Chemical compound [NH4+] QGZKDVFQNNGYKY-UHFFFAOYSA-O 0.000 claims abstract description 5
- 239000002243 precursor Substances 0.000 claims abstract 3
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 claims description 27
- 150000005215 alkyl ethers Chemical class 0.000 claims description 23
- 125000004122 cyclic group Chemical group 0.000 claims description 20
- 125000000217 alkyl group Chemical group 0.000 claims description 15
- 239000003795 chemical substances by application Substances 0.000 claims description 14
- 238000006386 neutralization reaction Methods 0.000 claims description 14
- 229910052799 carbon Inorganic materials 0.000 claims description 12
- DNIAPMSPPWPWGF-UHFFFAOYSA-N Propylene glycol Chemical compound CC(O)CO DNIAPMSPPWPWGF-UHFFFAOYSA-N 0.000 claims description 9
- 239000013543 active substance Substances 0.000 claims description 8
- 235000014113 dietary fatty acids Nutrition 0.000 claims description 8
- 239000000194 fatty acid Substances 0.000 claims description 8
- 229930195729 fatty acid Natural products 0.000 claims description 8
- 150000004665 fatty acids Chemical class 0.000 claims description 8
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 claims description 8
- 238000007046 ethoxylation reaction Methods 0.000 claims description 7
- 229910001420 alkaline earth metal ion Inorganic materials 0.000 claims description 6
- 125000000129 anionic group Chemical group 0.000 claims description 6
- 241000370738 Chlorion Species 0.000 claims description 5
- LYCAIKOWRPUZTN-UHFFFAOYSA-N Ethylene glycol Chemical compound OCCO LYCAIKOWRPUZTN-UHFFFAOYSA-N 0.000 claims description 4
- 150000002500 ions Chemical class 0.000 claims description 4
- JBVOQKNLGSOPNZ-UHFFFAOYSA-N 2-propan-2-ylbenzenesulfonic acid Chemical compound CC(C)C1=CC=CC=C1S(O)(=O)=O JBVOQKNLGSOPNZ-UHFFFAOYSA-N 0.000 claims description 3
- XSQUKJJJFZCRTK-UHFFFAOYSA-N Urea Chemical compound NC(N)=O XSQUKJJJFZCRTK-UHFFFAOYSA-N 0.000 claims description 3
- ZZXDRXVIRVJQBT-UHFFFAOYSA-M Xylenesulfonate Chemical compound CC1=CC=CC(S([O-])(=O)=O)=C1C ZZXDRXVIRVJQBT-UHFFFAOYSA-M 0.000 claims description 3
- 239000003513 alkali Substances 0.000 claims description 3
- 229910001413 alkali metal ion Inorganic materials 0.000 claims description 3
- 229910001860 alkaline earth metal hydroxide Inorganic materials 0.000 claims description 3
- 229910000287 alkaline earth metal oxide Inorganic materials 0.000 claims description 3
- 239000004202 carbamide Substances 0.000 claims description 3
- 229940071118 cumenesulfonate Drugs 0.000 claims description 3
- KWIUHFFTVRNATP-UHFFFAOYSA-N glycine betaine Chemical compound C[N+](C)(C)CC([O-])=O KWIUHFFTVRNATP-UHFFFAOYSA-N 0.000 claims description 3
- 229910052500 inorganic mineral Inorganic materials 0.000 claims description 3
- 239000011707 mineral Substances 0.000 claims description 3
- 229940045136 urea Drugs 0.000 claims description 3
- 229940071104 xylenesulfonate Drugs 0.000 claims description 3
- 229920003171 Poly (ethylene oxide) Polymers 0.000 claims description 2
- WGCNASOHLSPBMP-UHFFFAOYSA-N hydroxyacetaldehyde Natural products OCC=O WGCNASOHLSPBMP-UHFFFAOYSA-N 0.000 claims description 2
- 150000003467 sulfuric acid derivatives Chemical class 0.000 claims description 2
- 125000004432 carbon atom Chemical group C* 0.000 claims 6
- 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 claims 2
- 230000002378 acidificating effect Effects 0.000 claims 2
- 239000008103 glucose Substances 0.000 claims 2
- VHUUQVKOLVNVRT-UHFFFAOYSA-N Ammonium hydroxide Chemical compound [NH4+].[OH-] VHUUQVKOLVNVRT-UHFFFAOYSA-N 0.000 claims 1
- NINIDFKCEFEMDL-UHFFFAOYSA-N Sulfur Chemical compound [S] NINIDFKCEFEMDL-UHFFFAOYSA-N 0.000 claims 1
- 150000008044 alkali metal hydroxides Chemical class 0.000 claims 1
- 239000000908 ammonium hydroxide Substances 0.000 claims 1
- 229960004756 ethanol Drugs 0.000 claims 1
- 229960004063 propylene glycol Drugs 0.000 claims 1
- 239000011593 sulfur Substances 0.000 claims 1
- 229910052717 sulfur Inorganic materials 0.000 claims 1
- 238000004140 cleaning Methods 0.000 abstract description 8
- 229910052784 alkaline earth metal Inorganic materials 0.000 abstract description 7
- 150000001342 alkaline earth metals Chemical class 0.000 abstract description 7
- XLYOFNOQVPJJNP-UHFFFAOYSA-M hydroxide Chemical compound [OH-] XLYOFNOQVPJJNP-UHFFFAOYSA-M 0.000 abstract description 5
- 229910052783 alkali metal Inorganic materials 0.000 abstract 1
- 150000001340 alkali metals Chemical class 0.000 abstract 1
- 239000000047 product Substances 0.000 description 25
- HEMHJVSKTPXQMS-UHFFFAOYSA-M Sodium hydroxide Chemical compound [OH-].[Na+] HEMHJVSKTPXQMS-UHFFFAOYSA-M 0.000 description 15
- 239000000243 solution Substances 0.000 description 12
- 230000003165 hydrotropic effect Effects 0.000 description 8
- 239000000463 material Substances 0.000 description 8
- QAOWNCQODCNURD-UHFFFAOYSA-L Sulfate Chemical compound [O-]S([O-])(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-L 0.000 description 7
- 238000004851 dishwashing Methods 0.000 description 6
- 238000004519 manufacturing process Methods 0.000 description 6
- 239000012670 alkaline solution Substances 0.000 description 5
- 230000019635 sulfation Effects 0.000 description 5
- 238000005670 sulfation reaction Methods 0.000 description 5
- 150000001721 carbon Chemical group 0.000 description 4
- VTHJTEIRLNZDEV-UHFFFAOYSA-L magnesium dihydroxide Chemical compound [OH-].[OH-].[Mg+2] VTHJTEIRLNZDEV-UHFFFAOYSA-L 0.000 description 4
- 235000012254 magnesium hydroxide Nutrition 0.000 description 4
- VEXZGXHMUGYJMC-UHFFFAOYSA-M Chloride anion Chemical compound [Cl-] VEXZGXHMUGYJMC-UHFFFAOYSA-M 0.000 description 3
- 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 3
- TWRXJAOTZQYOKJ-UHFFFAOYSA-L Magnesium chloride Chemical compound [Mg+2].[Cl-].[Cl-] TWRXJAOTZQYOKJ-UHFFFAOYSA-L 0.000 description 3
- 238000004458 analytical method Methods 0.000 description 3
- 150000001875 compounds Chemical class 0.000 description 3
- 239000011552 falling film Substances 0.000 description 3
- 239000004615 ingredient Substances 0.000 description 3
- 239000013067 intermediate product Substances 0.000 description 3
- 239000000347 magnesium hydroxide Substances 0.000 description 3
- 229910001862 magnesium hydroxide Inorganic materials 0.000 description 3
- 238000002156 mixing Methods 0.000 description 3
- 230000007935 neutral effect Effects 0.000 description 3
- 238000002360 preparation method Methods 0.000 description 3
- 238000012545 processing Methods 0.000 description 3
- 239000002002 slurry Substances 0.000 description 3
- 229910052708 sodium Inorganic materials 0.000 description 3
- 239000011734 sodium Substances 0.000 description 3
- 238000005406 washing Methods 0.000 description 3
- ZAMOUSCENKQFHK-UHFFFAOYSA-N Chlorine atom Chemical compound [Cl] ZAMOUSCENKQFHK-UHFFFAOYSA-N 0.000 description 2
- JLVVSXFLKOJNIY-UHFFFAOYSA-N Magnesium ion Chemical compound [Mg+2] JLVVSXFLKOJNIY-UHFFFAOYSA-N 0.000 description 2
- ZLMJMSJWJFRBEC-UHFFFAOYSA-N Potassium Chemical compound [K] ZLMJMSJWJFRBEC-UHFFFAOYSA-N 0.000 description 2
- QAOWNCQODCNURD-UHFFFAOYSA-N Sulfuric acid Chemical compound OS(O)(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-N 0.000 description 2
- 150000001298 alcohols Chemical class 0.000 description 2
- 239000002585 base Substances 0.000 description 2
- 150000001720 carbohydrates Chemical class 0.000 description 2
- 239000000460 chlorine Substances 0.000 description 2
- 229910052801 chlorine Inorganic materials 0.000 description 2
- 238000011161 development Methods 0.000 description 2
- 230000018109 developmental process Effects 0.000 description 2
- 125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 description 2
- 239000012467 final product Substances 0.000 description 2
- 229930182478 glucoside Natural products 0.000 description 2
- 150000008131 glucosides Chemical group 0.000 description 2
- 229910017053 inorganic salt Inorganic materials 0.000 description 2
- 229940096405 magnesium cation Drugs 0.000 description 2
- 235000011147 magnesium chloride Nutrition 0.000 description 2
- 235000010755 mineral Nutrition 0.000 description 2
- 230000003472 neutralizing effect Effects 0.000 description 2
- 238000012856 packing Methods 0.000 description 2
- 229910052700 potassium Inorganic materials 0.000 description 2
- 239000011591 potassium Substances 0.000 description 2
- 230000001180 sulfating effect Effects 0.000 description 2
- BDHFUVZGWQCTTF-UHFFFAOYSA-M sulfonate Chemical compound [O-]S(=O)=O BDHFUVZGWQCTTF-UHFFFAOYSA-M 0.000 description 2
- AKEJUJNQAAGONA-UHFFFAOYSA-N sulfur trioxide Chemical compound O=S(=O)=O AKEJUJNQAAGONA-UHFFFAOYSA-N 0.000 description 2
- QCYOIFVBYZNUNW-UHFFFAOYSA-N 2-(dimethylazaniumyl)propanoate Chemical compound CN(C)C(C)C(O)=O QCYOIFVBYZNUNW-UHFFFAOYSA-N 0.000 description 1
- 240000004160 Capsicum annuum Species 0.000 description 1
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical group [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 description 1
- BVKZGUZCCUSVTD-UHFFFAOYSA-L Carbonate Chemical compound [O-]C([O-])=O BVKZGUZCCUSVTD-UHFFFAOYSA-L 0.000 description 1
- SNRUBQQJIBEYMU-UHFFFAOYSA-N Dodecane Natural products CCCCCCCCCCCC SNRUBQQJIBEYMU-UHFFFAOYSA-N 0.000 description 1
- IAYPIBMASNFSPL-UHFFFAOYSA-N Ethylene oxide Chemical group C1CO1 IAYPIBMASNFSPL-UHFFFAOYSA-N 0.000 description 1
- KFZMGEQAYNKOFK-UHFFFAOYSA-N Isopropanol Chemical compound CC(C)O KFZMGEQAYNKOFK-UHFFFAOYSA-N 0.000 description 1
- 229910019440 Mg(OH) Inorganic materials 0.000 description 1
- LRHPLDYGYMQRHN-UHFFFAOYSA-N N-Butanol Chemical class CCCCO LRHPLDYGYMQRHN-UHFFFAOYSA-N 0.000 description 1
- 150000001336 alkenes Chemical group 0.000 description 1
- 150000004996 alkyl benzenes Chemical class 0.000 description 1
- 239000003945 anionic surfactant Substances 0.000 description 1
- 239000007864 aqueous solution Substances 0.000 description 1
- 238000005815 base catalysis Methods 0.000 description 1
- 230000009286 beneficial effect Effects 0.000 description 1
- 229910001423 beryllium ion Inorganic materials 0.000 description 1
- 150000007516 brønsted-lowry acids Chemical class 0.000 description 1
- 150000007528 brønsted-lowry bases Chemical class 0.000 description 1
- 230000015556 catabolic process Effects 0.000 description 1
- 239000013522 chelant Substances 0.000 description 1
- 238000006243 chemical reaction Methods 0.000 description 1
- 239000007859 condensation product Substances 0.000 description 1
- 239000006071 cream Substances 0.000 description 1
- NSFKBZXCXCJZDQ-UHFFFAOYSA-N cumene;sodium Chemical compound [Na].CC(C)C1=CC=CC=C1 NSFKBZXCXCJZDQ-UHFFFAOYSA-N 0.000 description 1
- 238000006731 degradation reaction Methods 0.000 description 1
- 238000004821 distillation Methods 0.000 description 1
- 238000009826 distribution Methods 0.000 description 1
- 125000003438 dodecyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])* 0.000 description 1
- 239000000975 dye Substances 0.000 description 1
- 230000000694 effects Effects 0.000 description 1
- 238000005516 engineering process Methods 0.000 description 1
- 239000004744 fabric Substances 0.000 description 1
- 230000002349 favourable effect Effects 0.000 description 1
- JEIPFZHSYJVQDO-UHFFFAOYSA-N ferric oxide Chemical compound O=[Fe]O[Fe]=O JEIPFZHSYJVQDO-UHFFFAOYSA-N 0.000 description 1
- 238000011049 filling Methods 0.000 description 1
- 230000008014 freezing Effects 0.000 description 1
- 238000007710 freezing Methods 0.000 description 1
- 229910001385 heavy metal Inorganic materials 0.000 description 1
- 125000001183 hydrocarbyl group Chemical group 0.000 description 1
- 125000004356 hydroxy functional group Chemical group O* 0.000 description 1
- 238000001802 infusion Methods 0.000 description 1
- 230000000266 injurious effect Effects 0.000 description 1
- 239000002563 ionic surfactant Substances 0.000 description 1
- 150000002632 lipids Chemical class 0.000 description 1
- 230000007774 longterm Effects 0.000 description 1
- 229910001629 magnesium chloride Inorganic materials 0.000 description 1
- 239000000395 magnesium oxide Substances 0.000 description 1
- CPLXHLVBOLITMK-UHFFFAOYSA-N magnesium oxide Inorganic materials [Mg]=O CPLXHLVBOLITMK-UHFFFAOYSA-N 0.000 description 1
- AXZKOIWUVFPNLO-UHFFFAOYSA-N magnesium;oxygen(2-) Chemical compound [O-2].[Mg+2] AXZKOIWUVFPNLO-UHFFFAOYSA-N 0.000 description 1
- 125000001421 myristyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 description 1
- 125000000913 palmityl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 description 1
- 238000005191 phase separation Methods 0.000 description 1
- 238000003672 processing method Methods 0.000 description 1
- 230000001737 promoting effect Effects 0.000 description 1
- 239000002994 raw material Substances 0.000 description 1
- 239000007787 solid Substances 0.000 description 1
- 235000013599 spices Nutrition 0.000 description 1
- 230000006641 stabilisation Effects 0.000 description 1
- 238000011105 stabilization Methods 0.000 description 1
- 125000004079 stearyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 description 1
- 238000003860 storage Methods 0.000 description 1
- 239000000126 substance Substances 0.000 description 1
- XTHPWXDJESJLNJ-UHFFFAOYSA-N sulfurochloridic acid Chemical compound OS(Cl)(=O)=O XTHPWXDJESJLNJ-UHFFFAOYSA-N 0.000 description 1
- 229910021653 sulphate ion Inorganic materials 0.000 description 1
- 238000005494 tarnishing Methods 0.000 description 1
- 230000008719 thickening Effects 0.000 description 1
- 239000004034 viscosity adjusting agent 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
- 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
- C11D11/00—Special methods for preparing compositions containing mixtures of detergents
- C11D11/04—Special methods for preparing compositions containing mixtures of detergents by chemical means, e.g. by sulfonating in the presence of other compounding ingredients followed by neutralising
Landscapes
- Chemical & Material Sciences (AREA)
- Life Sciences & Earth Sciences (AREA)
- Engineering & Computer Science (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Oil, Petroleum & Natural Gas (AREA)
- Wood Science & Technology (AREA)
- Organic Chemistry (AREA)
- Detergent Compositions (AREA)
Abstract
A concentrated aqueous surfactant solution containing alkyl ether sulfate and alkaline earth metal (preferably magnesium). The composition is a stable liquid suitable for forming cleaning products, especially cleaning solutions. This concentrated surfactant solution can be prepared as follows: the acid precursor is partially neutralized with a hydroxide or oxide of an alkaline earth metal, and then further neutralized with a hydroxide of an alkali metal or ammonium.
Description
Latest developments trend in the detergent industry develops towards the direction of selling denseer product to the human consumer.This trend is except reducing the demand to wrapping material, and its benefit can be used littler and lighter packing bottle, box or the like in addition, uses to the human consumer to bring convenience.The minimizing of wrapping material has alleviated again conversely and handled the load of putting refuse in environment.Because having expected this point, the target of detergent manufacturers is to produce the raw material with greater concn activated detergent composition all the time.This target is urging on manufacturerss' deallocation system concentration to increase day by day and the composition of long-term stability and the processing method of Development and Production said composition.
The invention provides the spissated water base or water-alcohol solution of stablizing of a kind of sulfated alkyl ether, it is preparation cleaning products, the especially useful component of dishwashing detergent liquid.
This solution contains alkaline-earth metal ions (known can promote the dishwashing detergent performance formula), but seldom contains or not chloride ion-containing or sulfate ion (it has injurious effects to the stability of concentrated solution with by the finished product of said concentrated solution manufacturing).
The present invention has also illustrated the two step neutralisations of making this composition.
This composition can be intactly as finished product, but preferably makes it to be mixed and made into finished product with other all composition.Purpose is to carry out said sulfation one N-process away from the place of mixing finished product.This method is beneficial to economy and makes flexibly and transport.
In the dish washing liquid of at least a portion anion surfactant, use magnesium cation to disclose in the prior art widely, for example English Patent 1524441 and 1551074 and the disclosed patent application 2010893 of Britain as performance promotor.
Among on January 9th, the 1979 disclosed US4133779, disclose out a kind of cleaning composition that contains anionic and non-ionic type semi-polarity tensio-active agent.It is suggested, can make the concentrated solution/cream of a kind of 45-95% of containing active surfactant (can be sulfated alkyl ether).With the magnesium hydroxide neutralization is one of many selection schemes, but does not introduce process detail, and does not propose to avoid the measure of chlorion or sulfate ion.Preferably add magnesium with the sal epsom form.These compositions contain 1% semi-polarity nonionic surface active agent at least.
November 4 disclosed European 039110 in 1981 described and should avoid or reduce chlorion and sulfate ion, because chlorion that adds or sulfate ion can increase freezing point temperature (being inorganic salt temperature during with crystalline deposit in finished product).The composition that sulfated alkyl ether and other tensio-active agents, especially linear alkylbenzene sulfonate and alkyl-sulphate make up in the finished product has been described in Europe 039110.These finished products are not spissated, so the content of sulfated alkyl ether about about 10%.Disclose with blended sodium/magnesium cation and neutralized.
Point out among the EP 181212 that published on May 14th, 1986: can be with suitable alkali or with avoiding adding chlorion or sulfate ion with alkyl oxide sulfuric acid and alkylsurfuric acid in the oxide compound of magnesium or the hydroxide slurry.This publication has also been introduced the cleaning composition that contains the 22-65wt% surfactant system, and this system is made up of anionic, non-ionic type and the amphoteric ionic surfactant mixture in organic solubilized agent/hydrotropic agent-water medium.But this openly is confined to be lower than 24%(weight) sulfated alkyl ether.
Among on September 25th, 1979 disclosed US 4169078 and on May 27th, the 1992 disclosed EP 487170, all discussed for light dirt liquid detergent and used neutralization method, but these are open all at the composition that contains alkyl benzene sulphonate (ABS).
Introduced among the US 4129515 that on December 12nd, 1978 announced for various washing composition vitriol and sulfonate and used neutralization method, this neutralization is finished with alkanolamine, and formed composition is mainly used on the fabric washing.
It is a kind of long-time and at the stable highly enriched sulfated alkyl ether solution of lay up period that the object of the invention is to provide.This composition has known alkaline-earth metal ions as performance promotor in the dish washing liquid.Yet this composition contains the chlorine or the sulfate ion of extremely low amount.
Another object of the present invention is to provide a kind of manufacturing this method for compositions.
Another purpose of the present invention is to provide to make and contains sulfated alkyl ether and by the method for the stable composition of the polyhydric aniorfic surfactant of carbohydrate deutero-.
A kind of aqueous solution, the counter ion bonded that wherein contains and select from alkalimetal ion, alkaline-earth metal ions or ammonium ion or its hybrid ionic, 50-90%(weigh) sulfated alkyl ether, 0.5%(is heavy at least but also contain) alkaline-earth metal (preferably magnesium) ion and small amounts of chlorine ion or sulfate ion.Especially the mol ratio between alkaline-earth metal and (chlorine and mineral sulfates ion sum) was preferably greater than 3: 2 greater than 1: 1.
These compositions can be with comprising the two neutralisation manufacturings that go on foot.The first step is used alkaline earth metal hydroxides, preferred magnesium hydroxide or alkaline earth metal oxide, and preferred magnesium oxide is in the part and the sulfated alkyl ether of acid type.Second step is at another kind of alkali, as further neutralizing under the sodium hydroxide existence.In neutral one or two-stage, can selectivity there be hydrocarbon chain alcohol, hydrotropic agent or other tensio-active agent, so that control viscosity and the stability of improving product.
It is heavy that cleaning composition of the present invention contains 50-90%(), preferred 60-80%(is heavy) sulfated alkyl ether, also containing at least simultaneously, 0.5%(weighs) preferably 1%(is heavy at least) alkaline-earth metal, preferably magnesium.This composition contains small amount of chloride or vitriol.(term herein " sulfate radical " is meant SO
2- 4, can be ion or inorganic salt.The vitriol of ethoxylated alcohol or other organic surface active agent got rid of in this term).
Said composition can also optionally comprise the mixture of 0-20% short chain alcohol, hydrotropic agent, other tensio-active agent or these materials.Said pure preferred alcohol and propylene glycol; The preferred cumene sulfonate of hydrotropic agent, xylenesulfonate or urea and so on anionic aromatics hydrotropic agent; The preferred nonionic surface active agent of other tensio-active agent, polyoxyethylene glycol or trimethyl-glycine.
Said sulfated alkyl ether composition comprises by C
10-C
20The pure primary alkyl ether sulfate of deriving and obtaining with the condensation product that on average is higher than 8 ethylene oxide groups.Said alcohol itself can be obtained by natural fat, Ziegler alkene structures or oxo process.Synthetic obtain examples of materials and comprise: Dobanol 23
(Shell Chemicals(UK) Ltd. sale), Ethyl 24
(Ethyl Corp. sale), C
13-C
15(67%C
13And 33%C
15) the pure mixture (Synprol that trade(brand)name Lutensol that BASF GmbH sells and ICI plc sell
) and Lial 125
(by Liquichemica
Italia sells).The examples of natural materials that can therefrom obtain said alcohol is Oleum Cocois, palm chilli oil and corresponding lipid acid.
Preferred C
12-C
15Sulfated alkyl ether, most preferably C
12-C
13Sulfated alkyl ether.
Traditional base catalysis ethoxylation method causes forming a kind of distribution of all ethoxylates, and institute's monster can obtain required mean value differently.Use has the distribute material of (treatment step produced because of using specific ethoxylation technology and distillation subsequently etc.) of ethoxylation in various degree and/or different ethoxylate can prepare mixture.The mean number of the ethoxylate group that every mole of sulfated alkyl ether molecule is contained should be less than 8, preferably less than 4.Being particularly suitable for of average ethoxylated levels about 0.8 uses among the present invention.
The sulfation of said alcohol ethoxylate can adopt any traditional sulfating agent, for example sulphur trioxide or chlorsulfonic acid.This sulfation process can be carried out in falling film reactor, batch reactor or other sulfation equipment that is suitable for.The preferred continuous processing that adopts falling film reactor is so that made the Degradation of unsettled acid surface active agent reduce to minimum before neutralization.
The present invention will make the completeness of sulfating reaction reach maximum all the time, so that reduce mineral sulfates or the muriatic content that exists in the composition of neutralization back.In order to control spissated surface-active compositions viscosity and subsequently processing and/or procedure of processing to be carried out easily, it may be useful adding short chain alcohol (2-5 carbon atom); For example can use ethanol, propylene glycol, Virahol and butanols, preferred alcohol.Also can use some hydrotropic agents as viscosity modifier/stabilization agent, for example can use cumene sulfonate, xylenesulfonate and urea.
Neutralization method
Neutralization method of the present invention is carried out in two steps.The first step is used the alcohol of the sulfated ethoxylated of alkaline-earth metal (preferably magnesium) oxyhydroxide or alkaline-earth metal (preferably magnesium) oxide compound slurries (its solids content preferably at least 30%) part neutralizing acid shape; This N-process preferably use traditional in and cyclic system carry out continuously, said system is provided with high-shear mixer (bronsted lowry acids and bases bronsted lowry mixes rapidly closely) in this system, pump and heat exchanger, make some then treatment stage that the neutral product enters next, remaining still turns back in this high-shear mixer.Product section treatment stage of leaving this system by next accounts for 6-25wt% usually, preferably accounts for 9-17wt%, and remaining product continuation is middle circulation at this.
Essential feature of the present invention is: the product P H in shell heat exchanger exit should be less than 4(preferably less than 3).By adding another kind of alkaline solution and alkaline earth metal hydroxides/oxide compound in this first step and in the cyclic system, can effectively control PH.This additional alkaline solution is as if there being then the preferably hydroxide solution of sodium, potassium or ammonium.
In case of necessity, by in this first step and in the cyclic system, adding other composition (as tensio-active agent) of short chain alcohol, hydrotropic agent or general use in washing composition, can control viscosity.In leaving and the concentration of the intermediate product of cyclic system, can utilize the method that in this neutralized system, adds entry to regulate.Can add other detergent ingredients, as nonionic surface active agent and/or trimethyl-glycine.
Make then to leave in first to feed in second and cyclic system, finish neutralization operation with the intermediate product of cyclic system is direct.Also comprise high speed shear mixing machine, pump and heat exchanger with cyclic system in second.The intermediate product of first heat exchanger mixes to finish neutralization operation with alkaline solution in the high speed shear mixing machine.Leave in this and the product P H of cyclic system is at least 7, be preferably 7-9, be preferably about 8.
Can use any suitable alkaline solution in second He in the cyclic system, preferred alkaline solution is the hydroxide solution of sodium, potassium and ammonium.
Short chain alcohol, hydrotropic agent, water or their mixture also can join in second and in the cyclic system, but via in first and cyclic system to add these compositions generally be more favourable.
Preferably (but be not must) make whole alkalimetal ions via in first and cyclic system add.
Further handle
For the cleaning composition that the present invention is made can be stored and be transported according to the requirement of manufacturing operation, Cai composition was mixed with extra detergent ingredients before packing and transportation.Used extra detergent ingredients will be by the producer from selecting the activeconstituents widely.For example, be essentially the additional surface promoting agent of anionic, non-ionic type or amphoteric ion type, alkanolamide and so on is urged infusion, opalizer, thickening material, anti-tarnishing agent, heavy metal chelant etc. and be may be used in the finished product dish washing liquid body composition.
Particularly preferred scheme is: concentrated sulfated alkyl ether composition of the present invention is mixed with one or more nonionic surface active agent, make the composition that is particularly suitable for dish washing liquid.There is concentration in nonionic surface active agent in the present composition, can be between the 0-50wt%.Have been found that the present invention is particularly suited for being used for making some final product composition having like this, wherein comprises those poly-hydroxy nonionic surface active agent of being derived and being obtained by carbohydrate.This nonionic surface active agent comprises polyhydroxy fatty acid amide class and alkyl polyglucoside class.
Preferred polyhydroxy fatty acid amide class comprises some alkyl N-methyl glucose amides like this, alkyl chain wherein can comprise 8-22 carbon atom (preferably containing 12-18 carbon atom), especially mainly contains the coco group N-methyl glucose amide of 12-14 carbon atom alkyl.The method that is applicable to these polyhydroxy fatty acid amides of preparation is disclosed among the WO 92/06984.
Preferred alkyl polyglucoside, the material that comprises the alkyl that about 12-18 carbon atom is wherein arranged and on average contain the polyglucoside hydrophilic radical of an about 1.5-4 glucoside unit.The alkyl polyglucoside that is suitable for, be dodecyl, tetradecyl, hexadecyl and octadecyl 21,31,41, May Day and six glucosides and composition thereof.Further specifying of relevant alkyl poly glucoside is stated among the EP 70074.
In preferred final product composition having, the amount of polyhydroxy fatty acid amide or alkyl polyglucoside or its mixture is 1wt% at least, preferably 5wt% at least.
Embodiment
Prepared a kind of cleaning composition according to the present invention, wherein contained:
AE 0.8S(acid type) 70%
Mg(OH)
2(33% slurries) 8%
NaOH(50% solution) 13%
Water 4.5%
Ethanol 4.5%
The number of the average ethoxylation group of per molecule sulfated alkyl ether is 0.8(AE 0.8S) the acid type sulfated alkyl ether, in falling film reactor, utilize the method manufacturing of the corresponding ethoxylated alcohol of continuous sulfation.Alkyl chain mainly is C
12And C
13(Dobanol 23 for the mixture of chain length
, provide by Shell).Be expelled to first in 1.5 tons/hour speed acid and cyclic system in high shear mixer in.Whole magnesium hydroxides that final composition is required, the sodium hydroxide solution with 60% is added among this system.Water and ethanol also are added in this first cyclic system.Leave in this and the part neutral vitriol of cyclic system, just the temperature during outflow heat exchanger is 40 ℃, and PH is 3.Then this vitriol is directly injected second and the high shear mixer of cyclic system.All the other sodium hydroxide solutions of 40% are also pumped into the neutralization operation of finishing vitriol in second cyclic system.Leave in second and the temperature of the product outflow heat exchanger of cyclic system is 40 ℃, PH is 8.
The product of producing in this example is found by analysis, wherein contains 1.1wt% magnesium, 0.6% muriate and 1.0% vitriol; Represent that by mol% they are respectively 0.045mol% magnesium, 0.016mol% muriate and 0.01mol% vitriol.The ratio of magnesium and (vitriol and muriate) is (0.045): (0.01+0.016), be 1.7: 1(or 1: 0.6).This product is a shelf-stable, because: even still do not have phase separation or viscosity variation after one week of storage down at 50 ℃.
The high activity surface active composition of present embodiment is by on average containing the alcohol (C that 8 oxyethyl groups and carbon chain lengths are 10 ethoxylation with per molecule
10AE8), other composition of coco group N-methyl glucose amide and following definition mixes, and is further processed and makes finished product, the percentage ratio of all compositions is weight % in the finished product:
Surfactant composition 20%
C
10AE8 8%
N-methyl glucose amide 8%
C
12/ C
14Trimethyl-glycine 2%
Ethanol 5%
Cumene sodium sulfonate 2%
Dyestuff/spices 1%
Water surplus
This finished product also is a package stability.
Reference examples 2
Replace magnesium hydroxide to prepare the concentrated surfactant composition of embodiment 1 again with magnesium chloride, make magnesium density identical (1.1%) in this composition:
Umber
AE 0.8S(acid type) 70
NaOH(50% solution) to PH8
Water 4.5
Ethanol 4.5
MgCl
24.3
This routine product finds wherein to contain (wt%) by analysis: 1.1% magnesium, 3.71% muriate and 0.32% vitriol; If do not contain by the mol% score: 0.045mol% magnesium, 0.11mol% muriate and 0.003mol% vitriol.Magnesium is (0.045) with the ratio of (vitriol and muriate): (0.11+0.003), and promptly 1: 2.5.
Though the concentrated surface-active compositions of this reference examples definition is stable, surface-active compositions but finds it is unsettled by embodiment 1 finished product of making of filling a prescription thus.
Reference examples 3
Add 4.3 parts of magnesium chlorides again, repeat to prepare the high active surfactant composition identical with embodiment 2.This spissated surface-active compositions instability is separated into three isolating phases rapidly.
The product of this example preparation finds wherein to contain (wt%) by analysis: 2.2% magnesium, 6.9% muriate and 0.32% vitriol are respectively 0.092mol% magnesium, 0.2mol% muriate and 0.003mol% vitriol by its content of mol%; Magnesium is (0.092) with the ratio of (carbonate and muriate): (0.2+0.003), and promptly 1: 2.2.
This spissated surfactant composition is unstable and be separated.
Claims (13)
1, a kind of detergent composition wherein contains the sulfated alkyl ether of 50-90wt% following formula:
In the formula: R is the alkyl that contains 10-20 carbon atom,
N is less than 8, and
M
(2)+Comprise alkalimetal ion, alkaline-earth metal ions, ammonium ion or its mixture;
But also contain alcohol, the water-soluble growing agent of anionic aromatics, tensio-active agent or its mixture of 0-20wt%2-5 carbon atom; The content that it is characterized in that alkaline-earth metal ions is greater than 0.5wt%, and the ratio between alkaline-earth metal ions and (muriate/chlorion and mineral sulfates/inorganic sulfur acid ion sum) was preferably greater than 3: 2 greater than 1: 1.
2, according to the composition of claim 1, wherein R is the alkyl that contains 95wt%12-15 carbon atom at least.
3, according to the composition of claim 2, wherein n is the mean number of ethoxylation group in the per molecule sulfated alkyl ether, on average less than 4.
4, according to the composition of claim 3, wherein n is the ethoxylation group mean number of per molecule sulfated alkyl ether, average about 0.8.
5, according to the composition of claim 1, M wherein
(2)+At least contain 0.5wt% magnesium.
6,, wherein contain ethanol, propylene glycol, cumene sulfonate, xylenesulfonate, urea, polyoxyethylene glycol, trimethyl-glycine or its mixture of 0-20wt% according to the composition of claim 1.
7, according to the composition of claim 1, wherein the effective concentration of sulfated alkyl ether is 60-80wt%.
8, in a kind of and the method for the acidic precursor of sulfated alkyl ether, comprising step:
ⅰ) with one or more alkali of the pulp-water liquid that comprises alkaline earth metal hydroxides, alkaline earth metal oxide or its mixture, the acidic precursor of the said sulfated alkyl ether that partly neutralizes, the PH that makes product is less than 4;
ⅱ) further in and ⅰ) product, make the PH of product be at least 7;
ⅲ) add the nonionogenic tenside that accounts for finished weight 0-50%;
It is characterized in that in continous way and cyclic system in carry out the step (ⅰ) of this method and (ⅱ), in loop be placed in-line, and the neutralization operation of carrying out step (ⅱ) with alkali metal hydroxide or ammonium hydroxide.
9, method according to Claim 8, wherein the nonionic surface active agent of step (ⅲ) comprises at least 1% polyhydroxy fatty acid amide, alkyl polyglucoside or its mixture.
10, according to the method for claim 9, wherein the nonionic surface active agent of step (ⅲ) comprises at least 5% polyhydroxy fatty acid amide, alkyl polyglucoside or its mixture.
11, method according to Claim 8, wherein said polyhydroxy fatty acid amide are derived by glucose and are obtained, and for example comprise the N-methyl glucose amide of the alkyl chain of 8-22 carbon atom.
12, according to the method for claim 11, wherein said polyhydroxy fatty acid amide is derived by glucose and is obtained, and for example comprises the N-methyl glucose amide of the alkyl chain of 12-18 carbon atom.
13, method according to Claim 8 wherein adds alcohol, the water-soluble growing agent of anionic aromatics, tensio-active agent or its mixture of 2-5 carbon atom in first and in the cyclic system in step (ⅰ).
Applications Claiming Priority (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| EP92202559.8 | 1992-08-21 | ||
| EP92202559 | 1992-08-21 |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| CN1086538A true CN1086538A (en) | 1994-05-11 |
| CN1047615C CN1047615C (en) | 1999-12-22 |
Family
ID=8210873
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| CN93118314A Expired - Fee Related CN1047615C (en) | 1992-08-21 | 1993-08-21 | Concentrated liquid detergent compositions and methods of making such compositions |
Country Status (10)
| Country | Link |
|---|---|
| EP (1) | EP0656046A4 (en) |
| JP (1) | JPH08500388A (en) |
| CN (1) | CN1047615C (en) |
| AU (1) | AU5015293A (en) |
| BR (1) | BR9306927A (en) |
| CA (1) | CA2142913C (en) |
| MA (1) | MA22957A1 (en) |
| TR (1) | TR27633A (en) |
| TW (1) | TW246686B (en) |
| WO (1) | WO1994004640A1 (en) |
Families Citing this family (11)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| GB9314410D0 (en) * | 1993-07-13 | 1993-08-25 | Jeyes Group Plc | Cleansing compositions |
| EP0816479B2 (en) * | 1996-06-28 | 2008-10-01 | The Procter & Gamble Company | Dishwashing compositions with improved resistance to gelling |
| DE102005042606A1 (en) | 2005-09-07 | 2007-03-08 | Basf Ag | Neutralization process |
| DE102005042604A1 (en) | 2005-09-07 | 2007-03-08 | Basf Ag | Neutralization process |
| DE102005042605A1 (en) | 2005-09-07 | 2007-03-08 | Basf Ag | Neutralization process |
| JP5465872B2 (en) * | 2008-12-15 | 2014-04-09 | 花王株式会社 | Anionic surfactant composition |
| CN105518117B (en) * | 2013-09-09 | 2018-08-10 | 宝洁公司 | The method for preparing liquid cleansing composition |
| EP2975107A1 (en) | 2014-07-16 | 2016-01-20 | Hayat Kimya Sanayi Anonim Sirketi | Hand dishwashing composition with improved foaming properties |
| JP6688613B2 (en) * | 2016-01-15 | 2020-04-28 | 株式会社ニイタカ | Liquid detergent composition |
| EP4249578A1 (en) | 2022-03-07 | 2023-09-27 | The Procter & Gamble Company | Processes for making concentrated surfactant blends |
| WO2023172859A1 (en) | 2022-03-07 | 2023-09-14 | The Procter & Gamble Company | Processes for making concentrated surfactant blends |
Family Cites Families (15)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US4133779A (en) * | 1975-01-06 | 1979-01-09 | The Procter & Gamble Company | Detergent composition containing semi-polar nonionic detergent and alkaline earth metal anionic detergent |
| CA1052223A (en) * | 1975-01-06 | 1979-04-10 | David S. Lambert | Detergent composition containing semi-polar nonionic detergent and alkaline earth metal anionic detergent |
| JPS5238507A (en) * | 1975-09-22 | 1977-03-25 | Kao Corp | Detergent composition |
| US4129515A (en) * | 1976-09-13 | 1978-12-12 | The Procter & Gamble Company | Heavy-duty liquid detergent and process |
| DE3168008D1 (en) * | 1980-04-24 | 1985-02-14 | Procter & Gamble | Liquid detergent compositions |
| US4316824A (en) * | 1980-06-26 | 1982-02-23 | The Procter & Gamble Company | Liquid detergent composition containing alkyl sulfate and alkyl ethoxylated sulfate |
| DE3264512D1 (en) * | 1981-04-03 | 1985-08-08 | Procter & Gamble | Liquid detergent compositions |
| DE3370164D1 (en) * | 1982-10-28 | 1987-04-16 | Procter & Gamble | Liquid detergent compositions |
| JPS6011593A (en) * | 1983-06-30 | 1985-01-21 | ライオン株式会社 | Liquid detergent composition |
| ES8708009A1 (en) * | 1984-11-07 | 1987-09-01 | Procter & Gamble | Liquid detergent compositions. |
| US4923635A (en) * | 1987-07-06 | 1990-05-08 | Colgate-Palmolive Company | Liquid detergent composition containing alkylbenzene sulfonate, alkyl ethanol ether sulfate, alkanolamide foam booster and magnesium and triethanolammonium ions |
| US5096622A (en) * | 1988-12-05 | 1992-03-17 | Colgate-Palmolive Company | Liquid detergent composition containing alkylbenzene sulfonate, alkyl ethonal ether sulfate, alkanolamide foam booster and magnesium and triethanolammonium ions |
| GB9021217D0 (en) * | 1990-09-28 | 1990-11-14 | Procter & Gamble | Liquid detergent compositions |
| ES2077250T3 (en) * | 1990-09-28 | 1995-11-16 | Procter & Gamble | COMPOSITIONS OF DETERGENTS CONTAINING ANIONIC SURFACE AGENTS, POLYHYDROXY-AMIDES OF FATTY ACIDS AND MAGNESIUM. |
| NZ240395A (en) * | 1990-11-21 | 1993-10-26 | Colgate Palmolive Co | Process for manufacture of concentrated liquid detergent containing magnesium alkylbenzene sulphonate and alkanolamide suds booster |
-
1993
- 1993-08-12 EP EP93920103A patent/EP0656046A4/en not_active Ceased
- 1993-08-12 BR BR9306927A patent/BR9306927A/en not_active IP Right Cessation
- 1993-08-12 WO PCT/US1993/007700 patent/WO1994004640A1/en not_active Application Discontinuation
- 1993-08-12 TR TR00720/93A patent/TR27633A/en unknown
- 1993-08-12 AU AU50152/93A patent/AU5015293A/en not_active Abandoned
- 1993-08-12 JP JP6506467A patent/JPH08500388A/en active Pending
- 1993-08-12 CA CA002142913A patent/CA2142913C/en not_active Expired - Fee Related
- 1993-08-19 MA MA23264A patent/MA22957A1/en unknown
- 1993-08-21 CN CN93118314A patent/CN1047615C/en not_active Expired - Fee Related
- 1993-11-04 TW TW82109241A patent/TW246686B/zh active
Also Published As
| Publication number | Publication date |
|---|---|
| TR27633A (en) | 1995-06-14 |
| TW246686B (en) | 1995-05-01 |
| CA2142913A1 (en) | 1994-03-03 |
| BR9306927A (en) | 1999-01-12 |
| CA2142913C (en) | 1999-05-18 |
| EP0656046A1 (en) | 1995-06-07 |
| WO1994004640A1 (en) | 1994-03-03 |
| AU5015293A (en) | 1994-03-15 |
| EP0656046A4 (en) | 1995-09-20 |
| JPH08500388A (en) | 1996-01-16 |
| CN1047615C (en) | 1999-12-22 |
| MA22957A1 (en) | 1994-04-01 |
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