EP0088866B1 - Wässrige stabile Suspension wasserunlöslicher, zum Binden von Calciumionen befähigter Silikate und deren Verwendung zur Herstellung von Wasch- und Reinigungsmitteln - Google Patents
Wässrige stabile Suspension wasserunlöslicher, zum Binden von Calciumionen befähigter Silikate und deren Verwendung zur Herstellung von Wasch- und Reinigungsmitteln Download PDFInfo
- Publication number
- EP0088866B1 EP0088866B1 EP83100470A EP83100470A EP0088866B1 EP 0088866 B1 EP0088866 B1 EP 0088866B1 EP 83100470 A EP83100470 A EP 83100470A EP 83100470 A EP83100470 A EP 83100470A EP 0088866 B1 EP0088866 B1 EP 0088866B1
- Authority
- EP
- European Patent Office
- Prior art keywords
- water
- suspensions
- component
- alkylphenolethoxylates
- 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
Links
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
- C11D7/00—Compositions of detergents based essentially on non-surface-active compounds
-
- C—CHEMISTRY; METALLURGY
- C11—ANIMAL OR VEGETABLE OILS, FATS, FATTY SUBSTANCES OR WAXES; FATTY ACIDS THEREFROM; DETERGENTS; CANDLES
- C11D—DETERGENT COMPOSITIONS; USE OF SINGLE SUBSTANCES AS DETERGENTS; SOAP OR SOAP-MAKING; RESIN SOAPS; RECOVERY OF GLYCEROL
- C11D3/00—Other compounding ingredients of detergent compositions covered in group C11D1/00
- C11D3/02—Inorganic compounds ; Elemental compounds
- C11D3/12—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
Definitions
- Sodium is preferred as the cation, but it can also be replaced by lithium, potassium, ammonium or magnesium.
- aluminum silicates the compounds defined above which are capable of binding calcium are referred to below as “aluminum silicates”. This applies in particular to the sodium aluminum silicates to be used with preference; all statements made for their use according to the invention and all statements regarding their production and properties apply accordingly to the entirety of all the compounds defined above.
- the aluminum silicates which are particularly suitable for use in detergents and cleaning agents have a calcium binding capacity of preferably 50 to 200 mg CaO / g of the anhydrous aluminum silicate. If reference is made to anhydrous aluminum silicate in the following, it means the state of the aluminum silicate which is reached after drying for one hour at 800 ° C. During this drying, the adhering and bound water is practically completely removed.
- the aluminum silicates are supplied or used, for example, as an aqueous suspension. This would involve certain improvements in the suspension properties - e.g. the suspension stability and the pumpability of the aluminum silicates dispersed in the aqueous phase are still desirable.
- the invention relates to aqueous, pumpable, stable suspensions of a water-insoluble silicate capable of binding calcium ions in the form of a finely divided, bound water-containing, synthetically produced, water-insoluble compound (A) of the general formula in the cat a cation exchangeable with calcium of the valence n, x is a number from 0.7 to 1.5, Me boron or aluminum and y is a number from 0.8 to 6, which as the dispersing component (B) nonylphenol Contain ethylene adducts, and which are characterized in that they contain the water-insoluble silicate capable of binding calcium ions in amounts of 0.5 to 80% by weight and as a dispersing component 0.5 to 6% by weight of a mixture of at least two different alkylphenol ethoxylates of the formula contain, where n is 2 to 7 in the alkylphenol ethoxylate used in the mixture and 8 to 15 in the other alkylphenol ethoxylate, R is an alkyl group
- R is, for example, -CH 3 , -C 2 H 5 , propyl, butyl, pentyl, hexyl, heptyl or octyl or preferably an alkyl group with 9 carbon atoms such as nonyl.
- the phenyl ring can be substituted with the radical R in the ortho, meta and / or para position.
- Mixtures of compounds of the formula 11 can also be used which, in addition to compounds with p-substituted phenyl ring, also compounds with o-substi contained phenyl ring. Mixtures are preferably used in which 90% of the compounds of the formula II have a p-substitution and 10% have an ortho-substitution.
- n is preferably 4 to 6, in particular 5, for the alkylphenol ethoxylate used in the mixture and preferably 8 to 12, in particular 9 or 10, for the other alkylphenol ethoxylate.
- component A is preferably crystalline.
- y is preferably a number from 1.3 to 4.
- crystalline component A is a type A zeolite.
- foam-suppressing additives i.e. Compounds that improve the solubility of the added dispersants in the aqueous phase.
- solubilizers i.e. Compounds that improve the solubility of the added dispersants in the aqueous phase.
- foam-suppressing substances for example foam-suppressing soap, silicone defoamers, foam-suppressing triazine derivatives, all of which are known and familiar to the person skilled in the art, can be used as foam suppressors.
- foam suppressors can be used as foam suppressors.
- solubilizing substances is also generally not necessary, but may be appropriate if the suspension according to the invention contains a hydrophilic, but sparingly water-soluble colloid, such as polyvinyl alcohol, as a stabilizing agent. It is advantageous e.g. a solubilizer - dimethyl sulfoxide is very suitable - if the concentration of a stabilizing agent of group 1, which is only slightly soluble in water, is higher than 1%.
- the proportion of the solubilizer in the total suspension can, for example, be of the same order of magnitude as the proportion of the stabilizing agent.
- Hydrotrophic agents such as, for example, benzenesulfonic acid, toluenesulfonic acid, xylenesulfonic acid or their water-soluble salts or also octyl sulfate are suitable.
- the aluminum silicates of component A to be used can be amorphous or crystalline products, it also being possible, of course, to use mixtures of amorphous and crystalline products and also partially crystalline products.
- the aluminum silicates can be naturally occurring or else synthetically produced products, the synthetically produced products being preferred. They can be prepared, for example, by reacting water-soluble silicates with water-soluble aluminates in the presence of water. For this purpose, aqueous solutions of the starting materials can be mixed with one another or a component present in the solid state can be reacted with the other component present as an aqueous solution.
- the desired aluminum silicates are also obtained by mixing the two components present in the solid state in the presence of water.
- Aluminum silicates can also be produced from Al (OH) 2 , A1 2 0 3 or SiO z by reaction with alkali silicate or aluminate solutions. The production can also be carried out by other known processes.
- the invention relates to aluminum silicates which have a three-dimensional space lattice structure.
- the preferred calcium binding capacity which is approximately in the range from 100 to 200 mg CaO / g AS, usually around 100 to 180 mg CaO / g AS, is found above all in compounds of the composition:
- This molecular formula comprises two types of different crystal structures (or their non-crystalline precursors), which also differ in their molecular formulas. They are:
- the amorphous or crystalline aluminum silicate present in aqueous suspension can be separated from the remaining aqueous solution by filtration and at temperatures of e.g. Dry 50 to 400 ° C. Depending on the drying conditions, the product contains more or less bound water.
- Such high drying temperatures are generally not recommended; Expediently, the temperature does not exceed 200 ° C. if the aluminum silicate is intended for use in detergents and cleaning agents.
- the aluminum silicates do not need to be dried at all after their preparation in order to prepare a suspension according to the invention; rather - and this is particularly advantageous - an aluminum silicate that is still moist from manufacture can be used.
- dried aluminum silicates can also be used to prepare suspensions according to the invention at medium temperatures, for example from 80 to 200 ° C., until the adhering liquid water has been removed.
- the particle size of the individual aluminum silicate particles can be different and e.g. are in the range between 0.1 ⁇ m and 0.1 mm. This refers to the primary particle size, i.e. the size of the particles obtained during the precipitation and, if appropriate, the subsequent crystallization. It is particularly advantageous to use aluminum silicates which consist of at least 80% by weight of particles with a size of 10 to 0.01 ⁇ m, in particular 8 to 0.1 ⁇ m.
- These aluminum silicates preferably no longer contain primary or secondary particles with diameters above 45 ⁇ m.
- Secondary particles are particles that are formed by agglomeration of the primary particles into larger structures.
- the use of the aluminum silicates which are still moist from their production for the production of the suspensions according to the invention has proven particularly useful since it has been found that the formation of secondary particles is practically completely prevented when these still moist products are used.
- powdered zeolite of type A with a particularly defined particle spectrum is used as component A.
- Such zeolite powder can according to DE-B 24 47 021, DE-B 2517218, DE-A 2652419, DE-A 26 51 420, DE-A 26 51 436, DE-A 26 51 437, D EA 26 51 445, D EA 26 51 485 can be produced. They then have the particle distribution curves given there.
- a powdery zeolite of type A can be used, which has the particle size distribution described in DE-A 26 51 485.
- the concentration of component A can preferably be 44 to 55% by weight, in particular 46 to 52% by weight and more.
- the alkylphenol ethoxylates (component B) can be used in any mixture, preferably in a ratio of 1: 9 to 9: 1, preferably 2: 3 to 3: 2, in particular 0.9: 1.1 to 1.1: 0.9 will.
- the concentration of this mixture in the aqueous suspension is 1 to 2% by weight, in particular 1.4 to 1.6% by weight. This concentration is sufficient to stabilize a suspension with a solids content of 50% by weight or more.
- the suspension according to the invention has the advantage that it is sedimentation-stable in the temperature range from 10 to 50 ° C. and has a pumpable consistency.
- a further advantage is that the alkylphenol ethoxylate is liquid at room temperature and therefore does not need to be heated.
- the known suspension has a lower sedimentation stability and, with the same type of incorporation, is not homogeneous at room temperature and is therefore more difficult to process.
- the aqueous suspensions can contain, in addition to the constituents A and B mentioned and, in addition to any starting materials for the production of these constituents, any remaining constituents, also further constituents in comparatively small amounts. If the suspension is to be further processed into detergents and cleaning agents, the additional substances present are of course expediently substances which are suitable as constituents of detergents and cleaning agents.
- an indication of the stability of the suspensions is provided by a simple test in which an aluminum silicate suspension of the desired concentration, e.g. 31% - is produced, which contains a dispersant according to the invention and optionally further substances, for example detergent components such as pentasodium triphosphate, in different amounts. The influence of the added substance can then be visually observed in the settling behavior of the suspension. After standing for 24 hours, a preferred suspension should generally be at most so far removed that the protruding clear or silicate particle-free solution does not make up more than 20%, preferably not more than 10%, in particular not more than 6% of the total height.
- the amount of additives should be kept in such a way that the suspension can still be pumped perfectly again after 12 hours, preferably after 24 hours and in particular also after 48 hours in the storage container and pipe or hose lines.
- the settling behavior of the suspension which may also contain other constituents, is checked at room temperature - with a total height of the suspension of 10 cm. They are perfectly pumpable even after 4 or 8 days. This information on the stability of the suspension also only gives indications; It depends on the individual case which suspension stability is to be set.
- suspension according to the invention is used as a stock suspension for prolonged storage in a reservoir from which it can be drawn off by pumping as required, it may be expedient to keep the proportion of other constituents, for example of detergents and cleaning agents, low or to dispense with them entirely.
- the suspensions can be prepared by simply mixing their constituents, the aluminum silicates, for example as such or, if appropriate, from their preparation, can be used already in a moist state or in an aqueous suspension. It is particularly advantageous if they are still moist from their manufacture Stir aluminum silicates into component B, for example as a filter cake.
- the suspensions according to the invention are distinguished by high stability and by further advantages. Their stabilizing effect is particularly valuable in the case of aluminum silicates with particle sizes from 5 to 30 pm. They are pumpable so that they allow easy handling of moist aluminum silicates.
- the suspensions can be pumped around perfectly even after long interruptions in the pumping process. Due to their high stability, the suspensions can also be transported in conventional tank and tank wagons without fear of the formation of unusable or disruptive residues. This makes the suspensions ideal as a form of delivery of aluminum silicates for delivery to detergent manufacturers, for example.
- the suspensions can be stored at room temperature or at higher temperatures, pumped through pipes or transported in some other way.
- the suspensions are usually handled at temperatures between room temperature - usually preferred - and around 60 ° C.
- the suspensions according to the invention are particularly suitable for further processing to appear dry, pourable or free-flowing products, for example for the production of powdered water softening agents, for. B. on the way of spray drying, suitable.
- the suspensions are therefore of considerable importance in the production of powdered aluminum silicates. There are no annoying residues when feeding the aqueous suspensions to the drying apparatus. It has also been shown that the suspensions of the invention enable processing to extremely dust-free products.
- suspensions according to the invention are already as such, i.e. usable without further processing, with or without further washing, bleaching and / or cleaning additives, for example as water softening agents, washing or cleaning agents and in particular as liquid abrasives with increased suspension stability.
- a particularly important use of the suspension is the further processing to give dry-appearing, free-flowing or free-flowing detergents and cleaning agents which contain further compounds in addition to the suspension components.
- the suspensions according to the invention are particularly suitable for the production of powder detergents.
- an aqueous, flowable premix of the individual constituents of the agents is used and converted into a pourable product in the usual way.
- the aluminum silicates defined above are used in the form of the suspension according to the invention.
- the suspensions according to the invention can be processed into solid, pourable washing and cleaning agents by any known method.
- a suspension according to the invention - for example from a storage container - is mixed with at least one washing, bleaching or cleaning component of the agent to be prepared and the mixture is then processed by any process converted into the powdered product.
- a complexing agent is advantageously added, i.e. a compound that is able to complexly bind the alkaline earth metal ions responsible for water hardness, especially magnesium and calcium ions.
- the suspension according to the invention is preferably combined with at least one water-soluble surfactant which does not belong to the possible components of component B.
- the suspensions according to the invention can be combined with substances capable of binding water of crystallization, expediently by spraying the suspension onto the compounds which are capable of binding water of crystallization and which have been introduced into a mixer, so that an ultimately solid, dry-appearing product is obtained with constant mixing.
- the suspensions according to the invention when mixed as a “slurry”, are preferably subjected to the atomization drying with at least one further washing, bleaching or cleaning compound. This shows further surprising advantages of the claimed aluminum silicate suspension. It has been shown that very low-dust products can be obtained when using suspensions according to the invention in the spray drying. The products obtained by spray drying have a high calcium binding capacity and are easily wettable.
- Detergents which have been produced using the suspension described above can be composed in various ways. In general, they contain at least one water-soluble surfactant which does not belong to the dispersants used according to the invention and which are present in the claimed aluminum silicate suspensions. In general, they contain, in addition to at least one further compound which has a washing, bleaching or cleaning action and is inorganic or organic, a calcium-binding compound such as Aluminum silicate defined above. In addition, other customary auxiliaries and additives, which are usually present in smaller amounts, can be present in such agents.
- a zeolite A filter cake is stirred with water and stabilizer.
- Homogeneity and flow behavior are assessed according to the school grading system after the storage period.
- the viscosity is measured fresh, but does not change with homogeneous samples during the storage period.
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)
- Detergent Compositions (AREA)
- Silicates, Zeolites, And Molecular Sieves (AREA)
- Emulsifying, Dispersing, Foam-Producing Or Wetting Agents (AREA)
- Solid-Sorbent Or Filter-Aiding Compositions (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Distillation Of Fermentation Liquor, Processing Of Alcohols, Vinegar And Beer (AREA)
- Paper (AREA)
- Agricultural Chemicals And Associated Chemicals (AREA)
- Medicines Containing Material From Animals Or Micro-Organisms (AREA)
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
AT83100470T ATE20537T1 (de) | 1982-03-17 | 1983-01-20 | Waessrige stabile suspension wasserunloeslicher, zum binden von calciumionen befaehigter silikate und deren verwendung zur herstellung von waschund reinigungsmitteln. |
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
DE3209631A DE3209631A1 (de) | 1982-03-17 | 1982-03-17 | Waessrige stabile suspension wasserunloeslicher, zum binden von calciumionen befaehigter silikate und deren verwendung zur herstellung von wasch- und reinigungsmitteln |
DE3209631 | 1982-03-17 |
Publications (2)
Publication Number | Publication Date |
---|---|
EP0088866A1 EP0088866A1 (de) | 1983-09-21 |
EP0088866B1 true EP0088866B1 (de) | 1986-06-25 |
Family
ID=6158458
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
EP83100470A Expired EP0088866B1 (de) | 1982-03-17 | 1983-01-20 | Wässrige stabile Suspension wasserunlöslicher, zum Binden von Calciumionen befähigter Silikate und deren Verwendung zur Herstellung von Wasch- und Reinigungsmitteln |
Country Status (13)
Families Citing this family (7)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
DE3401861A1 (de) * | 1983-09-06 | 1985-03-21 | Degussa Ag, 6000 Frankfurt | Waessrige stabile suspension wasserunloeslicher, zum binden von calciumionen befaehigter silikate, deren verwendung zur herstellung von phosphatsubstituten fuer wasch- und reinigungsmittel und phosphatsubstitute |
DE3412188A1 (de) * | 1984-04-02 | 1985-10-10 | Henkel KGaA, 4000 Düsseldorf | Waschmittel |
DE3444311A1 (de) * | 1984-12-05 | 1986-06-05 | Degussa Ag, 6000 Frankfurt | Waessrige stabile suspension wasserunloeslicher, zum binden von calciumionen befaehigter silikate und deren verwendung zur herstellung von wasch- und reinigungsmitteln |
JPS63177495A (ja) * | 1987-01-16 | 1988-07-21 | Sharp Corp | 半導体レ−ザ素子 |
US5174918A (en) * | 1987-06-06 | 1992-12-29 | Degussa Ag | Stable aqueous suspensions of detergent zeolites and four oxo-alcohol ethoxylates |
DE19501269A1 (de) * | 1995-01-18 | 1996-07-25 | Henkel Kgaa | Amorphes Alkalisilikat-Compound |
PT2359136T (pt) * | 2008-11-07 | 2019-05-17 | Hoffmann La Roche | Substâncias de enchimento de granulação fina para filmes de reacção fotométrica |
Family Cites Families (12)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
AT330930B (de) * | 1973-04-13 | 1976-07-26 | Henkel & Cie Gmbh | Verfahren zur herstellung von festen, schuttfahigen wasch- oder reinigungsmitteln mit einem gehalt an calcium bindenden substanzen |
US4083793A (en) * | 1973-05-23 | 1978-04-11 | Henkel Kommanditgesellschaft Auf Aktien | Washing compositions containing aluminosilicates and nonionics and method of washing textiles |
ATA800274A (de) * | 1974-10-04 | 1983-12-15 | Henkel Kgaa | Verfahren zum waschen bzw. bleichen von textilien sowie mittel dazu |
AT336153B (de) * | 1974-10-08 | 1977-04-25 | Henkel & Cie Gmbh | Wasseriges reinigungsmittel zum reinigen textiler flachenbelage |
US4169075A (en) * | 1974-10-10 | 1979-09-25 | Henkel Kommanditgesellschaft Auf Aktien | Process for the production of powdery washing agents by spray-drying |
DE2517218B2 (de) * | 1975-04-18 | 1977-05-05 | Henkel & Cie GmbH, 4000 Düsseldorf; Deutsche Gold- und Silber-Scheideanstalt vormals Roessler, 6000 Frankfurt | Kristallines zeolithpulver des typs a |
AT362481B (de) * | 1976-02-06 | 1981-05-25 | Henkel Kgaa | Stabile, pumpfaehige, als vorratssuspension geeignete waesserige suspension von wasserun- loeslichen, zum binden von calcium befaehigten silikaten |
DE2615698A1 (de) * | 1976-04-09 | 1977-10-20 | Henkel & Cie Gmbh | Stabile suspensionen wasserunloeslicher, zum binden von calciumionen befaehigter silikate und deren verwendung zur herstellung von wasch- und reinigungsmitteln |
US4409136A (en) * | 1977-01-31 | 1983-10-11 | Colgate Palmolive Company | Molecular sieve zeolite-built detergent paste |
BE874420A (fr) * | 1978-03-02 | 1979-08-23 | Unilever Nv | Procede de production de compositions detergentes |
DE2856087A1 (de) * | 1978-12-23 | 1980-07-10 | Henkel Kgaa | Verfahren zur herstellung weisser, optische aufheller und kationenaustauschfaehige alumosilikate enthaltender, pulverfoermiger waschmittel |
DE2907108A1 (de) * | 1979-02-23 | 1980-09-04 | Basf Ag | Verfahren zur herstellung lagerstabiler, pumpbarer und fliessfaehiger alumosilikat-suspensionen durch nassvermahlung |
-
1982
- 1982-03-17 DE DE3209631A patent/DE3209631A1/de active Granted
-
1983
- 1983-01-20 AT AT83100470T patent/ATE20537T1/de not_active IP Right Cessation
- 1983-01-20 EP EP83100470A patent/EP0088866B1/de not_active Expired
- 1983-01-20 DE DE8383100470T patent/DE3364223D1/de not_active Expired
- 1983-02-10 DK DK056983A patent/DK158520C/da not_active IP Right Cessation
- 1983-02-14 FI FI830493A patent/FI830493L/fi not_active Application Discontinuation
- 1983-02-15 NO NO830511A patent/NO830511L/no unknown
- 1983-02-24 SU SU833556254A patent/SU1443805A3/ru active
- 1983-03-01 ES ES520187A patent/ES8505832A1/es not_active Expired
- 1983-03-10 JP JP58038365A patent/JPS58168698A/ja active Granted
- 1983-03-14 BR BR8301254A patent/BR8301254A/pt not_active IP Right Cessation
- 1983-03-15 US US06/475,394 patent/US4486331A/en not_active Expired - Fee Related
- 1983-03-16 KR KR1019830001055A patent/KR910001604B1/ko not_active Expired
- 1983-03-17 CA CA000423867A patent/CA1200456A/en not_active Expired
Also Published As
Publication number | Publication date |
---|---|
DK56983A (da) | 1983-09-18 |
EP0088866A1 (de) | 1983-09-21 |
BR8301254A (pt) | 1983-11-22 |
FI830493A0 (fi) | 1983-02-14 |
ES520187A0 (es) | 1985-06-16 |
US4486331A (en) | 1984-12-04 |
NO830511L (no) | 1983-09-19 |
FI830493A7 (fi) | 1983-09-18 |
SU1443805A3 (ru) | 1988-12-07 |
CA1200456A (en) | 1986-02-11 |
DK158520B (da) | 1990-05-28 |
DK56983D0 (da) | 1983-02-10 |
JPH0357959B2 (enrdf_load_stackoverflow) | 1991-09-03 |
DE3364223D1 (en) | 1986-07-31 |
FI830493L (fi) | 1983-09-18 |
ATE20537T1 (de) | 1986-07-15 |
DE3209631A1 (de) | 1983-09-29 |
ES8505832A1 (es) | 1985-06-16 |
KR840004158A (ko) | 1984-10-10 |
DE3209631C2 (enrdf_load_stackoverflow) | 1988-02-25 |
KR910001604B1 (ko) | 1991-03-16 |
JPS58168698A (ja) | 1983-10-05 |
DK158520C (da) | 1990-10-29 |
Similar Documents
Publication | Publication Date | Title |
---|---|---|
DE2527388C3 (de) | Verwendung stabiler Suspensionen wasserunlöslicher, zum Binden von Calciumionen befähigter Silikate zur Herstellung von Wasch- und Reinigungsmitteln | |
EP0185660B1 (de) | Stabilisierte, wässrige zeolith-suspension | |
EP0016344B1 (de) | Verfahren zur Herstellung lagerstabiler, pumpbarer und fliessfähiger Alumosilikat-Suspensionen durch Nassvermahlung | |
DE2907791A1 (de) | Reinigungsmittel und verfahren zu ihrer herstellung | |
EP0183945B1 (de) | Wässrige stabile Suspension wasserunlöslicher, zum Binden von Calciumionen befähigter Silikate und deren Verwendung zur Herstellung von Wasch- und Reinigungsmitteln | |
EP0088866B1 (de) | Wässrige stabile Suspension wasserunlöslicher, zum Binden von Calciumionen befähigter Silikate und deren Verwendung zur Herstellung von Wasch- und Reinigungsmitteln | |
EP0195127B1 (de) | Waschmittelbuilder | |
DE2426691C3 (enrdf_load_stackoverflow) | ||
EP0279040B1 (de) | Waschmittelbuilder | |
EP0144492B1 (de) | Wässrige stabile Suspensionen wasserunlöslicher Silikate und deren Verwendung zur Herstellung von Phosphatsubstituten für Wasch- und Reinigungsmittel | |
DE2501698C2 (de) | Optische Aufheller enthaltende Gemische und Verfahren zu deren Herstellung | |
EP0191187B1 (de) | Waschmittelbuilder | |
EP0294694B1 (de) | Wässrige stabile Suspension wasserunlöslicher, zum Binden von Calciumionen befähigter Silikate und deren Verwendung zur Herstellung von Wasch- und Reinigungsmitteln | |
EP0504564B1 (de) | Wässrige stabile Suspension wasserunlöslicher, zum Binden von Calciumionen befähigter Silikate und deren Verwendung zur Herstellung von Wasch- und Reinigungsmitteln | |
EP0294574A2 (de) | Wässrige stabile Suspension wasserunlöslicher zum Binden von Calciumionen befähigter Silikate und deren Verwendung zur Herstellung von Wasch- und Reinigungsmitteln | |
EP0279038B1 (de) | Waschmittelbuilder | |
WO1992003510A1 (de) | Zweikomponentenmittel zur koagulation von lacken, wachsen und beschichtungsmitteln | |
DE3818657A1 (de) | Waessrige stabile suspension wasserunloeslicher, zum binden von calciumionen befaehigter silikate und deren verwendung zur herstellung von wasch- und reinigungsmitteln | |
EP0279039B1 (de) | Waschmittelbuilder | |
DE2246896A1 (de) | Verfahren zur herstellung von aufschlaemmungen von optischen aufhellern aus der gruppe der triazolyl-stilbene | |
DE3210480C2 (de) | Verfahren zur Herstellung von Zeolithaufschlämmungen mit guter statischer und dynamischer Stabilität | |
DE1467637A1 (de) | Verfahren zur Herstellung von Reinigungsmitteln |
Legal Events
Date | Code | Title | Description |
---|---|---|---|
PUAI | Public reference made under article 153(3) epc to a published international application that has entered the european phase |
Free format text: ORIGINAL CODE: 0009012 |
|
17P | Request for examination filed |
Effective date: 19830120 |
|
AK | Designated contracting states |
Designated state(s): AT BE CH DE FR GB IT LI NL SE |
|
GRAA | (expected) grant |
Free format text: ORIGINAL CODE: 0009210 |
|
AK | Designated contracting states |
Kind code of ref document: B1 Designated state(s): AT BE CH DE FR GB IT LI NL SE |
|
REF | Corresponds to: |
Ref document number: 20537 Country of ref document: AT Date of ref document: 19860715 Kind code of ref document: T |
|
ITF | It: translation for a ep patent filed | ||
REF | Corresponds to: |
Ref document number: 3364223 Country of ref document: DE Date of ref document: 19860731 |
|
ET | Fr: translation filed | ||
PLBE | No opposition filed within time limit |
Free format text: ORIGINAL CODE: 0009261 |
|
STAA | Information on the status of an ep patent application or granted ep patent |
Free format text: STATUS: NO OPPOSITION FILED WITHIN TIME LIMIT |
|
26N | No opposition filed | ||
PGFP | Annual fee paid to national office [announced via postgrant information from national office to epo] |
Ref country code: NL Payment date: 19890131 Year of fee payment: 9 |
|
PGFP | Annual fee paid to national office [announced via postgrant information from national office to epo] |
Ref country code: DE Payment date: 19901217 Year of fee payment: 9 |
|
PGFP | Annual fee paid to national office [announced via postgrant information from national office to epo] |
Ref country code: SE Payment date: 19901218 Year of fee payment: 9 |
|
PGFP | Annual fee paid to national office [announced via postgrant information from national office to epo] |
Ref country code: AT Payment date: 19910102 Year of fee payment: 9 |
|
PGFP | Annual fee paid to national office [announced via postgrant information from national office to epo] |
Ref country code: GB Payment date: 19910111 Year of fee payment: 9 Ref country code: CH Payment date: 19910111 Year of fee payment: 9 |
|
PGFP | Annual fee paid to national office [announced via postgrant information from national office to epo] |
Ref country code: FR Payment date: 19910123 Year of fee payment: 9 |
|
ITTA | It: last paid annual fee | ||
PGFP | Annual fee paid to national office [announced via postgrant information from national office to epo] |
Ref country code: BE Payment date: 19911224 Year of fee payment: 10 |
|
PG25 | Lapsed in a contracting state [announced via postgrant information from national office to epo] |
Ref country code: GB Effective date: 19920120 Ref country code: AT Effective date: 19920120 |
|
PG25 | Lapsed in a contracting state [announced via postgrant information from national office to epo] |
Ref country code: SE Effective date: 19920121 |
|
PG25 | Lapsed in a contracting state [announced via postgrant information from national office to epo] |
Ref country code: LI Effective date: 19920131 Ref country code: CH Effective date: 19920131 |
|
PG25 | Lapsed in a contracting state [announced via postgrant information from national office to epo] |
Ref country code: NL Effective date: 19920801 |
|
NLV4 | Nl: lapsed or anulled due to non-payment of the annual fee | ||
REG | Reference to a national code |
Ref country code: GB Ref legal event code: PCNP |
|
PG25 | Lapsed in a contracting state [announced via postgrant information from national office to epo] |
Ref country code: FR Effective date: 19920930 |
|
REG | Reference to a national code |
Ref country code: CH Ref legal event code: PL |
|
PG25 | Lapsed in a contracting state [announced via postgrant information from national office to epo] |
Ref country code: DE Effective date: 19921001 |
|
REG | Reference to a national code |
Ref country code: FR Ref legal event code: ST |
|
PG25 | Lapsed in a contracting state [announced via postgrant information from national office to epo] |
Ref country code: BE Effective date: 19930131 |
|
BERE | Be: lapsed |
Owner name: DEGUSSA A.G. Effective date: 19930131 |
|
EUG | Se: european patent has lapsed |
Ref document number: 83100470.0 Effective date: 19920806 |