EP0595919B1 - Procede de stabilisation de suspensions aqueuses de zeolites - Google Patents
Procede de stabilisation de suspensions aqueuses de zeolites Download PDFInfo
- Publication number
- EP0595919B1 EP0595919B1 EP92915813A EP92915813A EP0595919B1 EP 0595919 B1 EP0595919 B1 EP 0595919B1 EP 92915813 A EP92915813 A EP 92915813A EP 92915813 A EP92915813 A EP 92915813A EP 0595919 B1 EP0595919 B1 EP 0595919B1
- Authority
- EP
- European Patent Office
- Prior art keywords
- alkyl
- alcohol
- suspensions
- carbon atoms
- formula
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Expired - Lifetime
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- 239000010457 zeolite Substances 0.000 title claims abstract description 27
- 238000000034 method Methods 0.000 title claims abstract description 14
- 230000000087 stabilizing effect Effects 0.000 title claims description 7
- 239000007900 aqueous suspension Substances 0.000 title claims description 5
- 239000000725 suspension Substances 0.000 claims abstract description 31
- -1 poly(ethyleneglycol) Polymers 0.000 claims abstract description 29
- HNPSIPDUKPIQMN-UHFFFAOYSA-N dioxosilane;oxo(oxoalumanyloxy)alumane Chemical compound O=[Si]=O.O=[Al]O[Al]=O HNPSIPDUKPIQMN-UHFFFAOYSA-N 0.000 claims abstract description 24
- 229910021536 Zeolite Inorganic materials 0.000 claims abstract description 19
- 125000000217 alkyl group Chemical group 0.000 claims abstract description 19
- 229930182470 glycoside Natural products 0.000 claims abstract description 18
- 125000004432 carbon atom Chemical group C* 0.000 claims abstract description 11
- 239000007787 solid Substances 0.000 claims description 5
- 125000002791 glucosyl group Chemical group C1([C@H](O)[C@@H](O)[C@H](O)[C@H](O1)CO)* 0.000 claims description 2
- 150000002170 ethers Chemical class 0.000 abstract description 6
- 150000002191 fatty alcohols Chemical class 0.000 abstract description 5
- 239000002736 nonionic surfactant Substances 0.000 abstract description 4
- 229920000151 polyglycol Polymers 0.000 abstract description 4
- 239000010695 polyglycol Substances 0.000 abstract description 4
- 229920001223 polyethylene glycol Polymers 0.000 abstract 2
- 125000001931 aliphatic group Chemical group 0.000 abstract 1
- 125000003342 alkenyl group Chemical group 0.000 abstract 1
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 description 10
- 239000003381 stabilizer Substances 0.000 description 9
- 229910004298 SiO 2 Inorganic materials 0.000 description 6
- 239000013049 sediment Substances 0.000 description 6
- 229910017090 AlO 2 Inorganic materials 0.000 description 5
- IAYPIBMASNFSPL-UHFFFAOYSA-N Ethylene oxide Chemical compound C1CO1 IAYPIBMASNFSPL-UHFFFAOYSA-N 0.000 description 5
- 229910052681 coesite Inorganic materials 0.000 description 5
- 229910052906 cristobalite Inorganic materials 0.000 description 5
- 239000000377 silicon dioxide Substances 0.000 description 5
- 229910052682 stishovite Inorganic materials 0.000 description 5
- 229910052905 tridymite Inorganic materials 0.000 description 5
- 239000000203 mixture Substances 0.000 description 4
- 238000006384 oligomerization reaction Methods 0.000 description 4
- 239000011734 sodium Substances 0.000 description 4
- 230000006641 stabilisation Effects 0.000 description 4
- 238000011105 stabilization Methods 0.000 description 4
- XUJLWPFSUCHPQL-UHFFFAOYSA-N 11-methyldodecan-1-ol Chemical compound CC(C)CCCCCCCCCCO XUJLWPFSUCHPQL-UHFFFAOYSA-N 0.000 description 3
- 229910052784 alkaline earth metal Inorganic materials 0.000 description 3
- 238000004062 sedimentation Methods 0.000 description 3
- 238000003860 storage Methods 0.000 description 3
- 239000004094 surface-active agent Substances 0.000 description 3
- KBPLFHHGFOOTCA-UHFFFAOYSA-N 1-Octanol Chemical compound CCCCCCCCO KBPLFHHGFOOTCA-UHFFFAOYSA-N 0.000 description 2
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 2
- 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 2
- CDBYLPFSWZWCQE-UHFFFAOYSA-L Sodium Carbonate Chemical compound [Na+].[Na+].[O-]C([O-])=O CDBYLPFSWZWCQE-UHFFFAOYSA-L 0.000 description 2
- 150000001298 alcohols Chemical class 0.000 description 2
- 239000003513 alkali Substances 0.000 description 2
- 150000001342 alkaline earth metals Chemical class 0.000 description 2
- 230000000052 comparative effect Effects 0.000 description 2
- 235000014113 dietary fatty acids Nutrition 0.000 description 2
- NOPFSRXAKWQILS-UHFFFAOYSA-N docosan-1-ol Chemical compound CCCCCCCCCCCCCCCCCCCCCCO NOPFSRXAKWQILS-UHFFFAOYSA-N 0.000 description 2
- RTZKZFJDLAIYFH-UHFFFAOYSA-N ether Substances CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 description 2
- 239000000194 fatty acid Substances 0.000 description 2
- 229930195729 fatty acid Natural products 0.000 description 2
- 239000008103 glucose Substances 0.000 description 2
- 229930182478 glucoside Natural products 0.000 description 2
- BXWNKGSJHAJOGX-UHFFFAOYSA-N hexadecan-1-ol Chemical compound CCCCCCCCCCCCCCCCO BXWNKGSJHAJOGX-UHFFFAOYSA-N 0.000 description 2
- GLDOVTGHNKAZLK-UHFFFAOYSA-N octadecan-1-ol Chemical compound CCCCCCCCCCCCCCCCCCO GLDOVTGHNKAZLK-UHFFFAOYSA-N 0.000 description 2
- 229920000642 polymer Polymers 0.000 description 2
- 239000000126 substance Substances 0.000 description 2
- HLZKNKRTKFSKGZ-UHFFFAOYSA-N tetradecan-1-ol Chemical compound CCCCCCCCCCCCCCO HLZKNKRTKFSKGZ-UHFFFAOYSA-N 0.000 description 2
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 2
- CFOQKXQWGLAKSK-KTKRTIGZSA-N (13Z)-docosen-1-ol Chemical compound CCCCCCCC\C=C/CCCCCCCCCCCCO CFOQKXQWGLAKSK-KTKRTIGZSA-N 0.000 description 1
- ALSTYHKOOCGGFT-KTKRTIGZSA-N (9Z)-octadecen-1-ol Chemical compound CCCCCCCC\C=C/CCCCCCCCO ALSTYHKOOCGGFT-KTKRTIGZSA-N 0.000 description 1
- TVPWKOCQOFBNML-SEYXRHQNSA-N (z)-octadec-6-en-1-ol Chemical compound CCCCCCCCCCC\C=C/CCCCCO TVPWKOCQOFBNML-SEYXRHQNSA-N 0.000 description 1
- CFOQKXQWGLAKSK-UHFFFAOYSA-N 13-docosen-1-ol Natural products CCCCCCCCC=CCCCCCCCCCCCCO CFOQKXQWGLAKSK-UHFFFAOYSA-N 0.000 description 1
- ZCYVEMRRCGMTRW-UHFFFAOYSA-N 7553-56-2 Chemical compound [I] ZCYVEMRRCGMTRW-UHFFFAOYSA-N 0.000 description 1
- 229910018072 Al 2 O 3 Inorganic materials 0.000 description 1
- 102000005701 Calcium-Binding Proteins Human genes 0.000 description 1
- 108010045403 Calcium-Binding Proteins Proteins 0.000 description 1
- VEXZGXHMUGYJMC-UHFFFAOYSA-M Chloride anion Chemical compound [Cl-] VEXZGXHMUGYJMC-UHFFFAOYSA-M 0.000 description 1
- KRKNYBCHXYNGOX-UHFFFAOYSA-K Citrate Chemical compound [O-]C(=O)CC(O)(CC([O-])=O)C([O-])=O KRKNYBCHXYNGOX-UHFFFAOYSA-K 0.000 description 1
- 235000013162 Cocos nucifera Nutrition 0.000 description 1
- 244000060011 Cocos nucifera Species 0.000 description 1
- VGGSQFUCUMXWEO-UHFFFAOYSA-N Ethene Chemical compound C=C VGGSQFUCUMXWEO-UHFFFAOYSA-N 0.000 description 1
- 239000005977 Ethylene Substances 0.000 description 1
- 208000007976 Ketosis Diseases 0.000 description 1
- BPQQTUXANYXVAA-UHFFFAOYSA-N Orthosilicate Chemical compound [O-][Si]([O-])([O-])[O-] BPQQTUXANYXVAA-UHFFFAOYSA-N 0.000 description 1
- 239000004435 Oxo alcohol Substances 0.000 description 1
- 229920000388 Polyphosphate Polymers 0.000 description 1
- GOOHAUXETOMSMM-UHFFFAOYSA-N Propylene oxide Chemical compound CC1CO1 GOOHAUXETOMSMM-UHFFFAOYSA-N 0.000 description 1
- 239000004115 Sodium Silicate Substances 0.000 description 1
- 229920002472 Starch Polymers 0.000 description 1
- QAOWNCQODCNURD-UHFFFAOYSA-L Sulfate Chemical compound [O-]S([O-])(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-L 0.000 description 1
- 150000001323 aldoses Chemical class 0.000 description 1
- 229910052783 alkali metal Inorganic materials 0.000 description 1
- 150000001340 alkali metals Chemical class 0.000 description 1
- 125000005466 alkylenyl group Chemical group 0.000 description 1
- 229910000323 aluminium silicate Inorganic materials 0.000 description 1
- JYIBXUUINYLWLR-UHFFFAOYSA-N aluminum;calcium;potassium;silicon;sodium;trihydrate Chemical compound O.O.O.[Na].[Al].[Si].[K].[Ca] JYIBXUUINYLWLR-UHFFFAOYSA-N 0.000 description 1
- 125000000129 anionic group Chemical group 0.000 description 1
- 150000001720 carbohydrates Chemical class 0.000 description 1
- 229960000541 cetyl alcohol Drugs 0.000 description 1
- 238000006243 chemical reaction Methods 0.000 description 1
- 229910001603 clinoptilolite Inorganic materials 0.000 description 1
- 229940096386 coconut alcohol Drugs 0.000 description 1
- 150000001875 compounds Chemical class 0.000 description 1
- MWKFXSUHUHTGQN-UHFFFAOYSA-N decan-1-ol Chemical compound CCCCCCCCCCO MWKFXSUHUHTGQN-UHFFFAOYSA-N 0.000 description 1
- 239000003599 detergent Substances 0.000 description 1
- JYIMWRSJCRRYNK-UHFFFAOYSA-N dialuminum;disodium;oxygen(2-);silicon(4+);hydrate Chemical compound O.[O-2].[O-2].[O-2].[O-2].[O-2].[O-2].[Na+].[Na+].[Al+3].[Al+3].[Si+4] JYIMWRSJCRRYNK-UHFFFAOYSA-N 0.000 description 1
- 239000006185 dispersion Substances 0.000 description 1
- 238000009826 distribution Methods 0.000 description 1
- 229960000735 docosanol Drugs 0.000 description 1
- LQZZUXJYWNFBMV-UHFFFAOYSA-N dodecan-1-ol Chemical compound CCCCCCCCCCCCO LQZZUXJYWNFBMV-UHFFFAOYSA-N 0.000 description 1
- 229910052675 erionite Inorganic materials 0.000 description 1
- 150000002148 esters Chemical class 0.000 description 1
- 150000004665 fatty acids Chemical class 0.000 description 1
- 230000002349 favourable effect Effects 0.000 description 1
- 239000011521 glass Substances 0.000 description 1
- 150000002338 glycosides Chemical class 0.000 description 1
- 125000002887 hydroxy group Chemical group [H]O* 0.000 description 1
- 229910052500 inorganic mineral Inorganic materials 0.000 description 1
- 239000011630 iodine Substances 0.000 description 1
- 229910052740 iodine Inorganic materials 0.000 description 1
- 150000002584 ketoses Chemical class 0.000 description 1
- 239000007791 liquid phase Substances 0.000 description 1
- 238000004519 manufacturing process Methods 0.000 description 1
- 239000011707 mineral Substances 0.000 description 1
- 229910052680 mordenite Inorganic materials 0.000 description 1
- 229940043348 myristyl alcohol Drugs 0.000 description 1
- GOQYKNQRPGWPLP-UHFFFAOYSA-N n-heptadecyl alcohol Natural products CCCCCCCCCCCCCCCCCO GOQYKNQRPGWPLP-UHFFFAOYSA-N 0.000 description 1
- ALSTYHKOOCGGFT-MDZDMXLPSA-N oleyl alcohol Chemical compound CCCCCCCC\C=C\CCCCCCCCO ALSTYHKOOCGGFT-MDZDMXLPSA-N 0.000 description 1
- 229940055577 oleyl alcohol Drugs 0.000 description 1
- XMLQWXUVTXCDDL-UHFFFAOYSA-N oleyl alcohol Natural products CCCCCCC=CCCCCCCCCCCO XMLQWXUVTXCDDL-UHFFFAOYSA-N 0.000 description 1
- LBIYNOAMNIKVKF-FPLPWBNLSA-N palmitoleyl alcohol Chemical compound CCCCCC\C=C/CCCCCCCCO LBIYNOAMNIKVKF-FPLPWBNLSA-N 0.000 description 1
- LBIYNOAMNIKVKF-UHFFFAOYSA-N palmitoleyl alcohol Natural products CCCCCCC=CCCCCCCCCO LBIYNOAMNIKVKF-UHFFFAOYSA-N 0.000 description 1
- 235000011837 pasties Nutrition 0.000 description 1
- 238000005191 phase separation Methods 0.000 description 1
- 150000003009 phosphonic acids Chemical class 0.000 description 1
- 235000011007 phosphoric acid Nutrition 0.000 description 1
- 150000003014 phosphoric acid esters Chemical class 0.000 description 1
- 150000003016 phosphoric acids Chemical class 0.000 description 1
- 229910052615 phyllosilicate Inorganic materials 0.000 description 1
- 229920005646 polycarboxylate Polymers 0.000 description 1
- 239000001205 polyphosphate Substances 0.000 description 1
- 235000011176 polyphosphates Nutrition 0.000 description 1
- 238000002360 preparation method Methods 0.000 description 1
- 238000005086 pumping Methods 0.000 description 1
- 230000009257 reactivity Effects 0.000 description 1
- 150000003839 salts Chemical class 0.000 description 1
- 229920006395 saturated elastomer Polymers 0.000 description 1
- 150000004760 silicates Chemical class 0.000 description 1
- 229910000029 sodium carbonate Inorganic materials 0.000 description 1
- 239000011780 sodium chloride Substances 0.000 description 1
- FAPWRFPIFSIZLT-UHFFFAOYSA-M sodium chloride Inorganic materials [Na+].[Cl-] FAPWRFPIFSIZLT-UHFFFAOYSA-M 0.000 description 1
- 239000001509 sodium citrate Substances 0.000 description 1
- 229910052911 sodium silicate Inorganic materials 0.000 description 1
- 238000001694 spray drying Methods 0.000 description 1
- 235000019698 starch Nutrition 0.000 description 1
- 239000008107 starch Substances 0.000 description 1
- 238000003756 stirring Methods 0.000 description 1
- BDHFUVZGWQCTTF-UHFFFAOYSA-M sulfonate Chemical compound [O-]S(=O)=O BDHFUVZGWQCTTF-UHFFFAOYSA-M 0.000 description 1
- 239000000230 xanthan gum Substances 0.000 description 1
- 229920001285 xanthan gum Polymers 0.000 description 1
- 229940082509 xanthan gum Drugs 0.000 description 1
- 235000010493 xanthan gum Nutrition 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
- C11D1/66—Non-ionic compounds
- C11D1/825—Mixtures of compounds all of which are non-ionic
- C11D1/8255—Mixtures of compounds all of which are non-ionic containing a combination of compounds differently alcoxylised or with differently alkylated chains
-
- 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
- C11D1/825—Mixtures of compounds all of which are non-ionic
-
- C—CHEMISTRY; METALLURGY
- C11—ANIMAL OR VEGETABLE OILS, FATS, FATTY SUBSTANCES OR WAXES; FATTY ACIDS THEREFROM; DETERGENTS; CANDLES
- C11D—DETERGENT COMPOSITIONS; USE OF SINGLE SUBSTANCES AS DETERGENTS; SOAP OR SOAP-MAKING; RESIN SOAPS; RECOVERY OF GLYCEROL
- C11D3/00—Other compounding ingredients of detergent compositions covered in group C11D1/00
- C11D3/02—Inorganic compounds ; Elemental compounds
- C11D3/12—Water-insoluble compounds
- C11D3/124—Silicon containing, e.g. silica, silex, quartz or glass beads
- C11D3/1246—Silicates, e.g. diatomaceous earth
- C11D3/128—Aluminium silicates, e.g. zeolites
- C11D3/1286—Stabilised aqueous aluminosilicate suspensions
-
- 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
- C11D1/00—Detergent compositions based essentially on surface-active compounds; Use of these compounds as a detergent
- C11D1/66—Non-ionic compounds
- C11D1/72—Ethers of polyoxyalkylene glycols
-
- 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
- C11D1/722—Ethers of polyoxyalkylene glycols having mixed oxyalkylene groups; Polyalkoxylated fatty alcohols or polyalkoxylated alkylaryl alcohols with mixed oxyalkylele groups
Definitions
- the invention relates to a method for stabilizing aqueous zeolite suspensions by adding alkyl and / or alkenyl glycosides.
- Zeolites in particular of the zeolite A type, are of particular importance as building blocks of modern detergents and have largely replaced the polyphosphates that have been used for decades. Their advantages lie not only in their high calcium binding capacity, but also in their high ecotoxicological compatibility [Tens.Surf. Det., 24 , 322 (1987)].
- the zeolites are obtained in the form of aqueous suspensions, which can either be stored as such and placed on the market, or can be subjected to spray drying.
- Zeolites have an extremely low solubility in water, so that suspensions of these substances are easy sediment. In the most favorable case, this leads to a phase separation, but usually considerable amounts of the solid separate out on the bottom of the vessels during storage, harden and then have to be separated, comminuted and resuspended with great technical effort. In other cases, the viscosity of the suspension increases so much that decanting or pumping over becomes difficult, if not impossible, and in any case is associated with considerable product losses.
- German patent application DE 33 30 220 A1 proposes adding 0.5 to 5% by weight of a mixture of fatty alcohol ethoxylates and fatty alcohol sulfates or fatty alcohol ether sulfates to the suspensions.
- German patent application DE 34 08 040 A1 describes a process for stabilizing 65% by weight zeolite A suspensions with the aid of 0.01 to 0.25% by weight xanthan gum and carboxyl- or hydroxyl-containing polymers.
- zeolite suspensions can also be stabilized at pH 9 to 10 by adding polyglycol ethers, fatty alcohol ether sulfates, fatty acid alkanolamides or fatty acid monoglycerides.
- PCT application WO-85/01039 describes a process for stabilizing aqueous zeolite A suspensions by adding a water-insoluble surfactant of the alcohol ethoxylate type and an auxiliary from the group of the anionic sulfate surfactants.
- non-ionic surfactants with a cloud point below 90 ° C. in particular fatty alcohol ethoxylates, can also be used as auxiliaries in addition to polymers, phosphoric acids or esters, sulfonate surfactants and sheet silicates to stabilize solid suspensions.
- nonionic surfactants such as, for example, adducts of ethylene and / or propylene oxide with C9 to C20 fatty alcohols, together with water-soluble salts, for example sodium carbonate, chloride, silicate or citrate, to stabilize zeolite suspensions is described in Japanese publication JP- A 57/061616 and JP-A 57/061615 known.
- the literature uses numerous other stabilizers, for example polycarboxylates with molecular weights above 1500, phosphonic acids, phosphoric acid esters, alkylbenzenesulfonates, layered silicates [DE-OS 27 388] , alkylphenol polyglycol ethers [DE 34 01 861 A1] , isotridecyl polyglycol ethers [DE 34 44 311 A1] and adducts of ethylene oxide with oxo alcohols [DE 37 19 042 A1] are known.
- the object of the invention was therefore to develop an improved method for stabilizing aqueous zeolite suspensions which is free from the disadvantages described.
- the invention relates to a method for stabilizing aqueous zeolite suspensions by adding Alkyl and / or alkenyl glycosides of the formula (I), R 1 O- (G) x (I) in which R 1 is an alkyl and / or alkenyl radical having 6 to 22 carbon atoms, G is a glycose unit which is derived from a sugar having 5 or 6 carbon atoms, and x is a number between 1 and 10.
- the use of the alkyl and / or alkenyl glycosides mentioned or their mixtures with one another can reliably stabilize suspensions of zeolites over a wide temperature range, in particular from 10 to 60 ° C.
- the suspensions have a high storage stability even over a longer period of time, can be conveyed through pipelines and can be easily poured out with only minor product losses.
- Zeolites are to be understood as meaning, if appropriate, water-containing alkali metal or alkaline earth metal aluminosilicates of the general formula (II) M 2 / z O ⁇ Al 2 O 3 ⁇ x SiO 2 ⁇ y H 2 O (II) where M stands for an alkali or alkaline earth metal of valence z, x for numbers from 1.8 to 12 and y for numbers from 0 to 8 [Chem.iuZt., 20 , 117 (1986)] .
- the aqueous suspensions can contain the zeolites in amounts of 20 to 60, preferably 25 to 50% by weight.
- alkyl and / or alkenyl glycosides to be used according to the invention are known substances. Processes for their preparation are based, for example, on glucose or starch, which are reacted with alcohols either directly or via the intermediate stage of the butyl glycosides [US 3,547,828, US 3,839,318, DE-A- 37 23 826] .
- the alkyl radical R 1 in formula (I) can be derived from primary saturated or monounsaturated alcohols having 6 to 22, preferably 12 to 18, carbon atoms. Typical examples are capronic alcohol, caprylic alcohol, capric alcohol, lauryl alcohol, myristyl alcohol, cetyl alcohol, palmitoleyl alcohol, stearyl alcohol, elaidyl alcohol, oleyl alcohol, petroselinyl alcohol, behenyl alcohol or erucyl alcohol and their technical mixtures.
- Alkyl or alkenyl glycosides of the formula (I), which are particularly suitable for the stabilization of aqueous zeolite suspensions, can be derived from aldoses or ketoses. Because of the higher reactivity and the technical availability, primarily the glycosides of the reducing saccharides and especially glucose come into consideration. The preferred alkyl and / or alkenyl glycosides are therefore the alkyl and / or alkenyl glucosides.
- the stabilizers used are alkyl glycosides of the formula (I) in which R 1 is a linear alkyl radical having 12 to 18 carbon atoms, G is a glucose unit and x is a number from 1 to 3 .
- the introduction of the stabilizers into the suspension is not critical and can, for. B. mechanically by stirring, optionally at elevated temperatures of 50 ° C. There is no chemical reaction.
- the alkyl and / or alkenyl glycosides can be added to the suspensions in amounts of 0.1 to 5, preferably 1 to 3% by weight, based on the suspension.
- Stabilizers used - according to the invention example : (30% by weight aqueous paste):
- Stabilizers used - comparative examples (30% by weight aqueous pastes):
- the stability of the suspensions was assessed over a period of 1 to 6 days according to the following criteria:
- the height of the liquid phase above the suspension was determined in mm.
- Residue in the beaker after decanting Specification in% by weight based on the suspension.
Landscapes
- Chemical & Material Sciences (AREA)
- Life Sciences & Earth Sciences (AREA)
- Engineering & Computer Science (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Oil, Petroleum & Natural Gas (AREA)
- Wood Science & Technology (AREA)
- Organic Chemistry (AREA)
- Inorganic Chemistry (AREA)
- Silicates, Zeolites, And Molecular Sieves (AREA)
- Detergent Compositions (AREA)
- Emulsifying, Dispersing, Foam-Producing Or Wetting Agents (AREA)
Claims (4)
- Procédé pour stabiliser des suspensions aqueuses de zéolithes par addition d'alkyl- et/ou d'alcénylglycosides de formule (I)
R1O-(G)x (I)
dans laquelle R1 désigne un groupe alkyle et/ou alcényle portant 6 à 22 atomes de carbone, G une unité glycose dérivant d'un sucre portant 5 ou 6 atomes de carbone et x un nombre entre 1 et 10. - Procédé selon la revendication 1, caractérisé en ce que l'on ajoute l'alkyl- et/ou alcénylglycoside à des suspensions aqueuses de zéolithe A présentant une concentration en solides de 20 à 60 % en poids.
- Procédé selon les revendications 1 et 2, caractérisé en ce que l'on met en oeuvre des alkylglycosides de formule (I) dans laquelle R1 représente un groupe alkyle linéaire portant 12 à 18 atomes de carbone, G une unité glucose et x des nombres allant de 1 à 3.
- Procédé selon les revendications 1 à 3, caractérisé en ce que les alkyl- et/ou alcénylglycosides sont ajoutés aux suspensions à des concentrations, rapportées à la suspension, de 0,1 à 0,5 % en poids.
Applications Claiming Priority (3)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| DE4124247A DE4124247A1 (de) | 1991-07-22 | 1991-07-22 | Verfahren zur stabilisierung von waessrigen zeolith-suspensionen |
| DE4124247 | 1991-07-22 | ||
| PCT/EP1992/001590 WO1993002171A1 (fr) | 1991-07-22 | 1992-07-13 | Procede de stabilisation de suspensions aqueuses de zeolites |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| EP0595919A1 EP0595919A1 (fr) | 1994-05-11 |
| EP0595919B1 true EP0595919B1 (fr) | 1996-08-21 |
Family
ID=6436732
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| EP92915813A Expired - Lifetime EP0595919B1 (fr) | 1991-07-22 | 1992-07-13 | Procede de stabilisation de suspensions aqueuses de zeolites |
Country Status (7)
| Country | Link |
|---|---|
| EP (1) | EP0595919B1 (fr) |
| JP (1) | JPH07502963A (fr) |
| AT (1) | ATE141640T1 (fr) |
| DE (2) | DE4124247A1 (fr) |
| DK (1) | DK0595919T3 (fr) |
| ES (1) | ES2090669T3 (fr) |
| WO (1) | WO1993002171A1 (fr) |
Families Citing this family (3)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| DE4203789A1 (de) * | 1992-02-10 | 1993-08-12 | Henkel Kgaa | Verfahren zur stabilisierung von waessrigen zeolith-suspensionen |
| US5759979A (en) * | 1993-04-05 | 1998-06-02 | Henkel Kommanditgesellschaft Auf Aktien | Detergent mixtures comprising APG and fatty alcohol polyglycol ether |
| JP2017141311A (ja) * | 2014-05-30 | 2017-08-17 | 協和化学工業株式会社 | 液状安定剤及び液状安定剤を含有する熱可塑性樹脂組成物 |
Family Cites Families (6)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US4169075A (en) * | 1974-10-10 | 1979-09-25 | Henkel Kommanditgesellschaft Auf Aktien | Process for the production of powdery washing agents by spray-drying |
| GR76286B (fr) * | 1981-09-28 | 1984-08-04 | Procter & Gamble | |
| AU3215784A (en) * | 1983-08-22 | 1985-03-29 | Aktien Henkel Kommanditgesellschaft Auf | Stabilisierte wasrige zeolith-suspension |
| ES2045012T3 (es) * | 1987-06-06 | 1994-01-16 | Degussa | Suspension acuosa estable de silicatos insolubles en agua, capacitados para la fijacion de iones de calcio y su utilizacion para la preparacion de agentes de lavado y limpieza. |
| DE4009533A1 (de) * | 1990-03-24 | 1991-09-26 | Henkel Kgaa | Schwachschaeumendes nichtionisches tensidgemisch |
| GB9025248D0 (en) * | 1990-11-20 | 1991-01-02 | Unilever Plc | Detergent compositions |
-
1991
- 1991-07-22 DE DE4124247A patent/DE4124247A1/de not_active Withdrawn
-
1992
- 1992-07-13 WO PCT/EP1992/001590 patent/WO1993002171A1/fr not_active Ceased
- 1992-07-13 DE DE59206964T patent/DE59206964D1/de not_active Expired - Fee Related
- 1992-07-13 EP EP92915813A patent/EP0595919B1/fr not_active Expired - Lifetime
- 1992-07-13 ES ES92915813T patent/ES2090669T3/es not_active Expired - Lifetime
- 1992-07-13 AT AT92915813T patent/ATE141640T1/de not_active IP Right Cessation
- 1992-07-13 JP JP5502572A patent/JPH07502963A/ja active Pending
- 1992-07-13 DK DK92915813.7T patent/DK0595919T3/da active
Also Published As
| Publication number | Publication date |
|---|---|
| JPH07502963A (ja) | 1995-03-30 |
| DK0595919T3 (da) | 1996-12-23 |
| WO1993002171A1 (fr) | 1993-02-04 |
| DE4124247A1 (de) | 1993-01-28 |
| EP0595919A1 (fr) | 1994-05-11 |
| ES2090669T3 (es) | 1996-10-16 |
| DE59206964D1 (de) | 1996-09-26 |
| ATE141640T1 (de) | 1996-09-15 |
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