EP0368137B1 - Method for the preparation of high-density zeolite granules - Google Patents
Method for the preparation of high-density zeolite granules Download PDFInfo
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- EP0368137B1 EP0368137B1 EP89120266A EP89120266A EP0368137B1 EP 0368137 B1 EP0368137 B1 EP 0368137B1 EP 89120266 A EP89120266 A EP 89120266A EP 89120266 A EP89120266 A EP 89120266A EP 0368137 B1 EP0368137 B1 EP 0368137B1
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- C—CHEMISTRY; METALLURGY
- C11—ANIMAL OR VEGETABLE OILS, FATS, FATTY SUBSTANCES OR WAXES; FATTY ACIDS THEREFROM; DETERGENTS; CANDLES
- C11D—DETERGENT COMPOSITIONS; USE OF SINGLE SUBSTANCES AS DETERGENTS; SOAP OR SOAP-MAKING; RESIN SOAPS; RECOVERY OF GLYCEROL
- C11D3/00—Other compounding ingredients of detergent compositions covered in group C11D1/00
- C11D3/16—Organic compounds
- C11D3/37—Polymers
- C11D3/3746—Macromolecular compounds obtained by reactions only involving carbon-to-carbon unsaturated bonds
- C11D3/3757—(Co)polymerised carboxylic acids, -anhydrides, -esters in solid and liquid compositions
- C11D3/3761—(Co)polymerised carboxylic acids, -anhydrides, -esters in solid and liquid compositions in solid compositions
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- 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
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- 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
- C11D17/00—Detergent materials or soaps characterised by their shape or physical properties
- C11D17/06—Powder; Flakes; Free-flowing mixtures; Sheets
- C11D17/065—High-density particulate detergent compositions
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- 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
Definitions
- the present invention relates to a new production process for zeolite-containing granules with a pronounced adsorption capacity for liquid to waxy active substances.
- the granules are characterized by a high density, i. H. a bulk density between 750 and 1,000 g / l (grams per liter) and are suitable for use in detergents and cleaning agents.
- Granules which contain zeolites, salts of (co) polymeric carboxylic acids and additionally small amounts of alkali metal silicates and which serve as carrier material for liquid detergent components, in particular nonionics, are described in DE-A-34 44 960.
- the bulk density of these granules produced by spray drying is a maximum of 700 g / l and is preferably between 500 and 650 g / l.
- Document EP-A-149 264 teaches that commercially available spray-dried zeolites or mixtures thereof are used for the same purpose with inorganic salts such as sodium sulfate.
- the bulk density of these spray products is in the range of 400 - 600 g / l.
- agglomerates containing zeolites and alkali silicates which have a bulk density of 300-700 g / l.
- a dry premix of zeolite and alkali metal silicate (mixing ratio 1: 1 to 1: 8) is sprayed with water in a granulator and agglomerated, whereupon the excess water is removed to a residual proportion of less than 5% by weight by drying .
- the granules are also suitable for adsorbing liquid detergent components, in particular from Nonionics.
- the main disadvantage is their high content of strongly alkaline-reacting alkali silicates, which severely limits their use in neutral to weakly alkaline-reacting detergents suitable for sensitive textiles and furthermore reduces the proportion of zeolite which is capable of ion exchange.
- bulk densities of over 700 g / l cannot be achieved.
- the present disadvantages are eliminated by the present invention and the production of granules with a high bulk density and a high proportion of ion-exchanging components is made possible.
- the invention relates to a process for the production of granules containing fine crystalline zeolite, sodium or potassium salts of polymeric or copolymeric carboxylic acids and water, characterized in that (a) in a first mixing stage a homogeneous, powdery mixture of zeolite and the Salt of the (co) polymeric carboxylic acid, this mixture (b) agglomerated in a second mixing and granulation stage and (c) the agglomerate obtained until a good is reached free-flowing granules with a bulk density of 750-1000 g / l after-drying.
- the granules which are produced by the process according to the invention generally contain (based on anhydrous substance) 60-80% by weight of zeolite, 2-15% by weight of a sodium salt of (co) polymeric carboxylic acids and 15-25% by weight.
- % Water including water bound to the zeolite.
- an anhydrous zeolite is understood to be a sodium zeolite dewatered at the annealing temperature.
- Granules with a content of 62-75% by weight, in particular 65-70% by weight, of zeolite (calculated as anhydrous) and 4-12% by weight, in particular 5-10% by weight of Na salt (co- ) polymeric carboxylic acids (water content: difference up to 100% by weight) are preferred.
- the granules For the production of the granules, it is expedient to start with spray-dried, finely powdered zeolite, which generally has a water content of 17-25% by weight, preferably 19-22% by weight.
- This water includes constitutional water and adhering moisture.
- 70-95 parts by weight, preferably 75-93 parts by weight and in particular 80-90 parts by weight of this water-containing zeolite are mixed with 2-12 parts by weight, preferably 4-10 parts by weight and in particular 5-8 parts by weight of the sodium salt of the polymeric or copolymeric carboxylic acid combined to form a homogeneous powder mixture.
- 15-25 parts by weight, preferably 18-23 parts by weight of water are mixed in with constant further mixing.
- the water is preferably sprayed onto the powder mixture kept in motion by means of nozzles, and this is further processed mechanically until granular agglomerates are formed.
- the still moist but free-flowing agglomerate is then dried, for example with hot flowing air or with hot combustion gases, the drying being carried out until the water added in the granulation stage to a proportion of less than 5 parts by weight, preferably less than 3 parts by weight is removed.
- further water components that were originally introduced with the zeolite or a (co) polymeric salt which is not used anhydrous can be removed during drying.
- Such "over-dried" granules can have application advantages, for example when added to detergents that contain moisture-sensitive active ingredients.
- the dewatering of the zeolite should preferably not be driven below a water content of 18% by weight in order to avoid a reduction in activity.
- the water content of the granules is expediently in a range in which the water-binding capacity of the zeolite is largely saturated, i.e. H. in which the zeolite has a total water content of 19-22% by weight (including constitutional water).
- Suitable zeolites are those of the zeolite A type. Mixtures of zeolite NaA and NaX can also be used, the proportion of the zeolite NaX in such mixtures advantageously being less than 30%, in particular less than 20%. Suitable zeolites have no particles larger than 30 ⁇ m and consist of at least 80% particles smaller than 10 ⁇ m. Their average particle size (volume distribution, measurement method: Coulter Counter) is 1 to 10 ⁇ m. Their calcium binding capacity, which is determined according to the information in DE-A-24 12 837 and is based on anhydrous substance, is in the range from 100 to 200 mg CaO / g.
- Examples of the homopolymeric and / or copolymeric carboxylic acids contained in the granules, in the present case as water-soluble salts, of which the sodium salts are preferred, are also polyacrylic acid, polymethacrylic acid and polymaleic acid, copolymers of acrylic acid with methacrylic acid or maleic acid with vinyl ethers, such as vinyl methyl ether or vinyl ethyl ether with vinyl esters, such as vinyl acetate or vinyl propionate, acrylamide, methacrylamide and with ethylene, propylene or styrene.
- copolymeric acids in which one of the components has no acid function the proportion thereof in the interest of sufficient water solubility is not more than 50 mole percent, preferably less than 30 mole percent.
- Copolymers of acrylic acid or methacrylic acid with maleic acid as described in more detail in EP 25 551 B1, have proven to be particularly suitable. These are copolymers which contain 50 to 90% by weight of acrylic acid or methacrylic acid and 50 to 10% by weight of maleic acid. Copolymers in which 45 to 85% by weight of acrylic acid and 55 to 15% by weight of maleic acid are present are particularly preferred.
- the molecular weight of the homo- or copolymeric polycarboxylates is generally 2,000 to 150,000, preferably 5,000 to 100,000.
- salts of (co) polymeric carboxylic acids in powder form often contain 5 to 15% by weight of moisture. This proportion of water is included in the calculation of the water balance, or the amount of water introduced into the pelletizing stage can be reduced by this proportion.
- the proportion of salts in the preparation of the compositions or in the composition of the finished granules is based on anhydrous salt.
- the granulation can be carried out batchwise or continuously in conventional mixing and granulating devices.
- B. pelletizers which consist of a horizontally arranged or inclined to the horizontal, cylindrical containers, in the longitudinal axis of which is equipped with a mixing tools and conveyor blades rotating shaft.
- the water can be supplied by spray nozzles mounted in the wall or on the hollow shaft. If work is carried out continuously, two consecutive mixers can be used, the dry premix being produced in the first mixer and the pelletizing taking place in the second mixer with the addition of water. Continuous work is also possible in a mixer, the powder streams being combined and homogenized in a first mixing section and the mixture being treated with water and agglomerating in a subsequent mixing section in a subsequent mixing section.
- the drying can be carried out by introducing hot gases in a third mixing section z. B. a fluidized bed, or after the granules have been discharged from the mixer, for example in a vibrating section, a free-fall dryer or in a thin layer on a conveyor belt. Finally coarse and fine particles are sieved. The coarse fractions are ground and mixed into the product, fine fractions or dust are returned to the granulation.
- the granules have a bulk density of 750-1000 g / l, usually that of 800-950 g / l. Due to their tight packing and their small pore volume, their absorption capacity for liquid or pasty detergent components, especially nonionics, is somewhat reduced compared to specifically lighter carrier grains, but is still 15 to a maximum of 20% by weight without any appreciable impairment of the free-flowing properties. This In view of the high packing density, the surprisingly high adsorption capacity is completely sufficient for the usual fields of application, in particular for use as a mixture component in detergents and cleaning agents.
- the granules can be impregnated with any liquid or paste-like or fat-like detergent constituents which cannot be incorporated into conventional powdered or granular detergents or cleaning agents in other ways or only with a loss of activity.
- foam inhibitors in particular paraffin hydrocarbons, silicones, silicone resins and bis-acylalkylenediamines derived from long-chain fatty acids, and mixtures thereof.
- Further adsorbable active ingredients are fatty acid alkylolamides and cationic plasticizers, such as quaternary ammonium salts containing long-chain fatty residues, and also fat-dissolving solvents, such as terpenes.
- the granules are preferably used as carrier grains for nonionic surfactants. This is another aspect of the invention.
- Suitable nonionic surfactants are alkoxylation products with 10 to 20 carbon atoms in the hydrophobic radical and 3 to 20 glycol ether groups. These include ethoxylation products of alcohols, vicinal diols, amines, thio alcohols, fatty acid amides and fatty acids. Alkylphenol polyglycol ethers with 5 to 12 carbon atoms in the alkyl radical and 3 to 10 ethylene glycol ether groups are also useful. Block polymers of ethylene oxide and propylene oxide, which are commercially available under the name Pluronics, are also suitable. Alkyl glycosides or alkyl polyglycosides and mixtures thereof with the ethoxylation products mentioned can also be used.
- Preferred nonionics which can be adsorbed on the granulate and together with it as a free-flowing mixture, are derived from alcohols with 12 to 18 carbon atoms which are saturated or olefinically unsaturated, linear or methyl-branched in the 2-position (oxo radical) could be.
- Their reaction products with ethylene oxide (EO) or propylene oxide (PO) are water-soluble or water-dispersible mixtures of compounds with different degrees of alkoxylation, the number of EO or PO groups given below corresponding to a statistical mean.
- Examples of preferred ethoxylated fatty alcohols are C12 ⁇ 18 coconut alcohols with 3 to 12 EO, C16 ⁇ 18 tallow alcohol with 4 to 16 EO, oleyl alcohol with 4 to 12 EO and ethoxylation products of corresponding chain and EO distribution available from other native fatty alcohol mixtures. From the series of ethoxylated oxo alcohols, for example, those of the composition C12 ⁇ 15 + 5 to 10 EO and C14 ⁇ C15 + 6 to 12 EO are suitable.
- ethoxylates are also suitable which contain EO groups and PO groups, e.g. B. C12 ⁇ 18 alcohols of the formula R- (PO) a - (EO) b or R- (EO) b - (PO) c , wherein a numbers from 1 to 3, b such from 5 to 20 and c mean those from 1 to 10 (b greater than c).
- the liquid, optionally heated, additives, in particular nonionics, can be applied to the granules by mixing, preferably spraying, the carrier material advantageously being kept in motion by suitable mixing devices. Further treatment of the granular adsorbate is not necessary. However, leaving the product to rest for several hours at high contents of applied liquid material can be expedient, since its diffusion into the interior of the grain takes some time. The treatment of the granules with the liquid additives leads to a further increase in the bulk density, which can rise to values of over 1,000 g / l.
- the grains can optionally be dusted with finely divided powders or coated on the surface.
- Suitable powdering agents have a grain size of 0.001 to at most 0.1 mm, preferably less than 0.05 mm and can be present in proportions of 0.03 to 3, preferably 0.05 mm to 2% by weight, based on the Additive-laden adsorbents can be used.
- finely powdered zeolites, silica airgel (Aerosil (R) ), colorless or colored pigments such as titanium dioxide are suitable. in the in general, however, such an aftertreatment is superfluous, especially since it does not improve the solution properties.
- the detergent additives can be combined and mixed in a known manner with the granular or pulverulent detergent, for example a tower spray powder and its mixtures with other powder components, such as persalts, enzyme granules, bleach activators or defoamers.
- the high bulk density and the favorable flushing behavior of the additives according to the invention are transferred to these complex mixtures.
- the detergents mixed together generally contain 10 to 40% by weight of the additive according to the invention.
- the granules according to the invention have a different grain structure than those which are produced by conventional granulation processes. This can also be demonstrated by electron micrographs. If, as is customary in conventional granulation processes, the powdery zeolite is placed in the mixer and a solution of the (co) polymeric salt is sprayed on, granules are formed which do not differ externally from the products according to the invention, except that their bulk density is significantly reduced.
- the images obtained with the scanning electron microscope show sections through two different granules on a magnification scale of 1: 2 500 (Figs. 1 and 2) and 1: 5 000 (Figs. 3 and 4). Both grains have the same qualitative and quantitative composition as in Example 1.
- Figures 1 and 3 show a grain, in the production of which the spray-dried zeolite was sprayed in a mixer with a 25% strength by weight aqueous solution of the copolymeric salt, granulated and then dried.
- Figures 2 and 4 show the grain structure of the according to the information from Example 1 manufactured product. The arrangement of the cubic zeolite particles in Figures 1 and 3 is completely random. Large pores change with strongly glued, irregularly structured aggregates. In Figures 2 and 4, the zeolite cubes are packed much denser and more uniformly. Individual parts are reminiscent of a structure comparable to a pavement or a brickwork. The pore size is also significantly reduced.
- the granulation was carried out in a mixing granulator, consisting of a horizontally arranged cylindrical mixer with a rotating shaft (Lödige type) rotating in the central axis, equipped with mixing elements, with a capacity of 130 liters and a knife mill connected to it, operated at a speed of 1200 to 1500 rpm .
- a mixing granulator 69.5 parts by weight of a synthetic, finely crystalline, spray-dried zeolite of the NaA type, containing 20% by weight of bound water, were mixed with 8.8 parts by weight of the powdered sodium salt of an acrylic acid-maleic acid copolymer (moisture content 8 % By weight) to a homogeneous powder mixture.
- the copolymer (Sokalan (R) CP5 from BASF, Ludwigshafen) had a molecular weight of approximately 70,000. After the mixing, which took about 20 seconds, 21.7 parts by weight of water were sprayed in over 90 seconds by means of nozzles and the mixture was granulated for a further 3 minutes with constant mixing. The granules leaving the mixer were dried in a fluidized bed with hot, flowing dry gases. The final product had the following composition: 72.9% by weight of zeolite (calculated as anhydrous) 9.3% by weight polymer salt (calculated anhydrous) 17.8 wt% water The water was practically completely bound to the zeolite, from which a water content of the zeolite of 19.7% by weight is calculated. After screening about 15% coarse grain, a sieve analysis showed the following grain distribution (the amount in% by weight remaining on the sieves is given): m 1.6 0.8 0.4 0.2 0.1 less than 0.1 % By weight 20th 29 23 14 8th 6
- the bulk density of the granules was 900 g / l.
- the granules were sprayed in a spray mixer with a liquid, nonionic surfactant heated to 40 ° C., consisting of a mixture of coconut and tallow alcohol reacted with 5 mol EO in a ratio of 1: 4. After a standing time of 1 hour, the adsorbates showed the following bulk weights: example % By weight nonionic g / l bulk density 1a 2nd 960 1b 6.5 995 1c 12.3 1,060
- the granules treated with the nonionic surfactant were free-flowing and had a perfect wash-in capacity, both as unblended powder and mixed with a powdery household detergent in a ratio of 1: 4.
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Description
Die vorliegende Erfindung betrifft ein neues Herstellungsverfahren für zeolithhaltige Granulate mit ausgeprägtem Adsorptionsvermögen für flüssige bis wachsartige Wirkstoffe. Die Granulate zeichnen sich durch eine hohe Dichte, d. h. ein Schüttgewicht zwischen 750 und 1 000 g/l (Gramm pro Liter) aus und eignen sich zum Einsatz in Wasch- und Reinigungsmittel.The present invention relates to a new production process for zeolite-containing granules with a pronounced adsorption capacity for liquid to waxy active substances. The granules are characterized by a high density, i. H. a bulk density between 750 and 1,000 g / l (grams per liter) and are suitable for use in detergents and cleaning agents.
Aus der EP-A-243 908 sind Granulate bekannt, die als Wasserenthärtungsmittel eingesetzt werden und die feinkristallinen Zeolith, Natriumsalze polymerer oder copolymerer Carbonsäuren sowie Natriumcitrat und Natriumcarbonat enthalten. Dabei wurden die Granulate durch das Versprühen einer wäßrigen Lösung des (co-)polymeren Salzes auf eine homogenisierte Mischung aus Zeolith, Citrat und Carbonat erhalten. Durch Sprühtrocknung von wäßrigen Aufschlämmungen hergestellte, feinpulvrige Zeolithe und Salze von (co-)polymeren Carbonsäuren enthaltende Granulate sind aus der DE-A-33 16 513 bekannt. Sie weisen ein Schüttgewicht von lediglich 560 - 610 g/l auf. Eine Lehre des Inhalts, daß derartige Granulate als Trägermaterial für flüssige bis wachsartige Waschmittelbestandteile brauchbar sind, ist diesem Dokument nicht zu entnehmen. Granulate, die Zeolithe, Salze (co-)polymerer Carbonsäuren und zusätzlich geringe Mengen an Alkalimetallsilikaten enthalten und als Trägermaterial für flüssige Waschmittelbestandteile, insbesondere Nonionics dienen, sind in der DE-A-34 44 960 beschrieben. Das Schüttgewicht dieser durch Sprühtrocknung hergestellten Granulate beträgt maximal 700 g/l und liegt vorzugsweise zwischen 500 und 650 g/l. Dokument EP-A-149 264 lehrt, daß man für den gleichen Zweck handelsübliche sprühgetrocknete Zeolithe bzw. deren Gemische mit anorganischen Salzen, wie Natriumsulfat, verwenden kann. Das Schüttgewicht dieser Sprühprodukte liegt im Bereich von 400 - 600 g/l. Aus EP-A-21 267 sind Agglomerate mit einem Gehalt an Zeolithen und Alkalisilikaten bekannt, die ein Schüttgewicht von 300 - 700 g/l aufweisen. Zu ihrer Herstellung wird ein trockenes Vorgemisch aus Zeolith und Alkalimetallsilikat (Mischungsverhältnis 1 : 1 bis 1 : 8) in einem Granulator mit Wasser besprüht und agglomeriert, worauf das überschüssige Wasser bis auf einen Restanteil von weniger als 5 Gew.-% durch Trocknung entfernt wird. Die Granulate eignen sich ebenfalls zum Adsorbieren flüssiger Waschmittelbestandteile, insbesondere von Nonionics. Nachteilig ist vor allem ihr hoher Gehalt an stark alkalisch reagierenden Alkalisilikaten, die ihren Einsatz in neutral bis schwach alkalisch reagierenden, für empfindliche Textilien geeigneten Waschmitteln stark einschränkt und überdies den Anteil des Ionenaustausch-fähigen Zeoliths vermindert. Außerdem lassen sich nach den Lehren dieses Dokumentes keine Schüttgewichte von über 700 g/l erzielen.From EP-A-243 908 granules are known which are used as water softening agents and which contain finely crystalline zeolite, sodium salts of polymeric or copolymeric carboxylic acids as well as sodium citrate and sodium carbonate. The granules were obtained by spraying an aqueous solution of the (co) polymeric salt onto a homogenized mixture of zeolite, citrate and carbonate. DE-A-33 16 513 discloses granules containing fine powdered zeolites and salts of (co) polymeric carboxylic acids which are produced by spray drying aqueous slurries. They have a bulk density of only 560 - 610 g / l. A teaching of the content that such granules can be used as carrier material for liquid to waxy detergent components is not to be found in this document. Granules which contain zeolites, salts of (co) polymeric carboxylic acids and additionally small amounts of alkali metal silicates and which serve as carrier material for liquid detergent components, in particular nonionics, are described in DE-A-34 44 960. The bulk density of these granules produced by spray drying is a maximum of 700 g / l and is preferably between 500 and 650 g / l. Document EP-A-149 264 teaches that commercially available spray-dried zeolites or mixtures thereof are used for the same purpose with inorganic salts such as sodium sulfate. The bulk density of these spray products is in the range of 400 - 600 g / l. From EP-A-21 267 agglomerates containing zeolites and alkali silicates are known which have a bulk density of 300-700 g / l. For their preparation, a dry premix of zeolite and alkali metal silicate (mixing ratio 1: 1 to 1: 8) is sprayed with water in a granulator and agglomerated, whereupon the excess water is removed to a residual proportion of less than 5% by weight by drying . The granules are also suitable for adsorbing liquid detergent components, in particular from Nonionics. The main disadvantage is their high content of strongly alkaline-reacting alkali silicates, which severely limits their use in neutral to weakly alkaline-reacting detergents suitable for sensitive textiles and furthermore reduces the proportion of zeolite which is capable of ion exchange. In addition, according to the teachings of this document, bulk densities of over 700 g / l cannot be achieved.
Durch die vorliegende Erfindung werden die aufgezeigten Nachteile beseitigt und die Herstellung von Granulaten mit hohem Schüttgewicht und hohem Anteil an ionenaustauschenden Bestandteilen ermöglicht.The present disadvantages are eliminated by the present invention and the production of granules with a high bulk density and a high proportion of ion-exchanging components is made possible.
Gegenstand der Erfindung ist ein Verfahren zur Herstellung von Granulaten mit einem Gehalt an feinkristallinem Zeolith, Natrium- oder Kaliumsalzen polymerer bzw. copolymerer Carbonsäuren und Wasser, dadurch gekennzeichnet, daß man (a) in einer ersten Mischstufe eine homogene, pulvrige Mischung aus Zeolith und dem Salz der (co-)polymeren Carbonsäure herstellt, dieses Gemisch (b) in einer zweiten Misch- und Granulationsstuffe agglomeriert und (c) das erhaltene Agglomerat bis zum Erreichen eines gut rieselfähigen Granulates mit einem Schüttgewicht von 750 - 1 000 g/l nachtrocknet.The invention relates to a process for the production of granules containing fine crystalline zeolite, sodium or potassium salts of polymeric or copolymeric carboxylic acids and water, characterized in that (a) in a first mixing stage a homogeneous, powdery mixture of zeolite and the Salt of the (co) polymeric carboxylic acid, this mixture (b) agglomerated in a second mixing and granulation stage and (c) the agglomerate obtained until a good is reached free-flowing granules with a bulk density of 750-1000 g / l after-drying.
Die Granulate, die nach dem erfindungsgemäßen Verfahren hergestellt werden, enthalten im allgemeinen (bezogen auf wasserfreie Substanz) 60 - 80 Gew.-% Zeolith, 2 - 15 Gew.-% eines Natriumsalzes (co-)polymerer Carbonsäuren und 15 - 25 Gew.-% Wasser einschließlich des an den Zeolith gebundenen Wassers. Als wasserfreier Zeolith wird in diesem Falle ein bei Glühtemperatur entwässerter Na-Zeolith verstanden. Granulate mit einem Gehalt an 62 - 75 Gew.-%, insbesondere 65 - 70 Gew.-% an Zeolith (wasserfrei gerechnet) und 4 - 12 Gew.-%, insbesondere 5 - 10 Gew.-% Na-Salz (co-)polymerer Carbonsäuren (Wassergehalt: Differenz bis 100 Gew.-%) sind bevorzugt.The granules which are produced by the process according to the invention generally contain (based on anhydrous substance) 60-80% by weight of zeolite, 2-15% by weight of a sodium salt of (co) polymeric carboxylic acids and 15-25% by weight. % Water, including water bound to the zeolite. In this case, an anhydrous zeolite is understood to be a sodium zeolite dewatered at the annealing temperature. Granules with a content of 62-75% by weight, in particular 65-70% by weight, of zeolite (calculated as anhydrous) and 4-12% by weight, in particular 5-10% by weight of Na salt (co- ) polymeric carboxylic acids (water content: difference up to 100% by weight) are preferred.
Zwecks Herstellung der Granulate geht man zweckmäßigerweise von sprühgetrocknetem, feinpulvrigem Zeolith aus, der im allgemeinen einen Wassergehalt von 17 - 25 Gew.-%, vorzugsweise 19 - 22 Gew.-% aufweist. Dieses Wasser schließt Konstitutionswasser und anhaftende Feuchtigkeit ein. 70 - 95 Gew.-teile, vorzugsweise 75 - 93 Gew.-teile und insbesondere 80 - 90 Gew.-teile dieses wasserhaltigen Zeoliths werden in einer Mischvorrichtung mit 2 - 12 Gew.-teilen, vorzugsweise 4 - 10 Gew.-teilen und insbesondere 5 - 8 Gew.-teilen des Natriumsalzes der polymeren bzw. copolymeren Carbonsäure zu einem homogenen Pulvergemisch vereinigt. Zwecks Agglomerierung werden unter ständigem weiteren Mischen 15 - 25 Gew.-teile, vorzugsweise 18 - 23 Gew.-teile Wasser zugemischt. Vorzugsweise wird das Wasser mittels Düsen auf das in Bewegung gehaltene Pulvergemisch aufgesprüht und dieses bis zur Ausbildung körniger Agglomerate mechanisch weiterbearbeitet.For the production of the granules, it is expedient to start with spray-dried, finely powdered zeolite, which generally has a water content of 17-25% by weight, preferably 19-22% by weight. This water includes constitutional water and adhering moisture. 70-95 parts by weight, preferably 75-93 parts by weight and in particular 80-90 parts by weight of this water-containing zeolite are mixed with 2-12 parts by weight, preferably 4-10 parts by weight and in particular 5-8 parts by weight of the sodium salt of the polymeric or copolymeric carboxylic acid combined to form a homogeneous powder mixture. For agglomeration, 15-25 parts by weight, preferably 18-23 parts by weight of water are mixed in with constant further mixing. The water is preferably sprayed onto the powder mixture kept in motion by means of nozzles, and this is further processed mechanically until granular agglomerates are formed.
Das noch feuchte aber bereits rieselfähige Agglomerat wird anschließend getrocknet, beispielsweise mit heißer strömender Luft bzw. mit heißen Verbrennungsgasen, wobei die Trocknung so weit geführt wird, bis das in der Granulationsstufe zugesetzte Wasser bis auf einen Anteil von weniger als 5 Gew.-teilen, vorzugsweise weniger als 3 Gew.-teilen entfernt ist. Zusätzlich können bei der Trocknung noch weitere Wasseranteile, die ursprünglich mit dem Zeolith bzw. einem nicht wasserfrei eingesetzten (co-)polymeren Salz eingebracht wurden, entfernt werden. Derartige "übertrocknete" Granulate können anwendungstechnische Vorteile aufweisen, beispielsweise beim Zusatz zu Waschmitteln, die feuchtigkeitsempfindliche Wirkstoffe enthalten. Vorzugsweise sollte jedoch die Entwässerung des Zeoliths nicht unter einen Wassergehalt von 18 Gew.-% getrieben werden, um eine Aktivitätsverminderung zu vermeiden. Zweckmäßigerweise liegt der Wassergehalt der Granulate in einem Bereich, bei dem das Wasserbindungsvermögen des Zeoliths weitgehend abgesättigt ist, d. h. bei dem der Zeolith einen Wassergehalt von insgesamt 19 - 22 Gew.-% (einschließlich Konstitutionswasser) besitzt.The still moist but free-flowing agglomerate is then dried, for example with hot flowing air or with hot combustion gases, the drying being carried out until the water added in the granulation stage to a proportion of less than 5 parts by weight, preferably less than 3 parts by weight is removed. In addition, further water components that were originally introduced with the zeolite or a (co) polymeric salt which is not used anhydrous can be removed during drying. Such "over-dried" granules can have application advantages, for example when added to detergents that contain moisture-sensitive active ingredients. However, the dewatering of the zeolite should preferably not be driven below a water content of 18% by weight in order to avoid a reduction in activity. The water content of the granules is expediently in a range in which the water-binding capacity of the zeolite is largely saturated, i.e. H. in which the zeolite has a total water content of 19-22% by weight (including constitutional water).
Geeignete Zeolithe sind solche vom Zeolith A-Typ. Brauchbar sind ferner Gemische aus Zeolith NaA und NaX, wobei der Anteil des Zeoliths NaX in derartigen Gemischen zweckmäßigerweise unter 30 %, insbesondere unter 20 % liegt. Geeignete Zeolithe weisen keine Teilchen mit einer Größe über 30 µm auf und bestehen zu wenigstens 80 % aus Teilchen einer Größe von weniger als 10 µm. Ihre mittlere Teilchengröße (Volumenverteilung, Meßmethode: Coulter Counter) beträgt 1 bis 10 µm. Ihr Calciumbindevermögen, das nach den Angaben der DE-A-24 12 837 bestimmt und auf wasserfreie Substanz bezogen wird, liegt im Bereich von 100 bis 200 mg CaO/g.Suitable zeolites are those of the zeolite A type. Mixtures of zeolite NaA and NaX can also be used, the proportion of the zeolite NaX in such mixtures advantageously being less than 30%, in particular less than 20%. Suitable zeolites have no particles larger than 30 µm and consist of at least 80% particles smaller than 10 µm. Their average particle size (volume distribution, measurement method: Coulter Counter) is 1 to 10 µm. Their calcium binding capacity, which is determined according to the information in DE-A-24 12 837 and is based on anhydrous substance, is in the range from 100 to 200 mg CaO / g.
Beispiele für die in den Granulaten enthaltenen homopolymeren und/oder copolymeren Carbonsäuren, vorliegend als wasserlösliche Salze, von denen die Natriumsalze bevorzugt werden, sind Polyacrylsäure, Polymethacrylsäure und Polymaleinsäure, Copolymere der Acrylsäure mit Methacrylsäure oder Maleinsäure mit Vinylethern, wie Vinylmethylether bzw. Vinylethylether, ferner mit Vinylestern, wie Vinylacetat oder Vinylpropionat, Acrylamid, Methacrylamid sowie mit Ethylen, Propylen oder Styrol. In solchen copolymeren Säuren, in denen eine der Komponenten keine Säurefunktion aufweist, beträgt deren Anteil im Interesse einer ausreichenden Wasserlöslichkeit nicht mehr als 50 Molprozent, vorzugsweise weniger als 30 molprozent. Als besonders geeignet haben sich Copolymere der Acrylsäure bzw. Methacrylsäure mit Maleinsäure erwiesen, wie sie beispielsweise in EP 25 551 B1 näher charakterisiert sind. Es handelt sich dabei um Copolymerisate, die 50 bis 90 Gew.-% Acrylsäure bzw. Methacrylsäure und 50 bis 10 Gew.-% Maleinsäure enthalten. Besonders bevorzugt sind solche Copolymere, in denen 45 bis 85 Gew.-% Acrylsäure und 55 bis 15 Gew.-% Maleinsäure anwesend sind. Das Molekulargewicht der homo- bzw. copolymeren Polycarboxylate beträgt im allgemeinen 2 000 bis 150 000, vorzugsweise 5 000 bis 100 000.Examples of the homopolymeric and / or copolymeric carboxylic acids contained in the granules, in the present case as water-soluble salts, of which the sodium salts are preferred, are also polyacrylic acid, polymethacrylic acid and polymaleic acid, copolymers of acrylic acid with methacrylic acid or maleic acid with vinyl ethers, such as vinyl methyl ether or vinyl ethyl ether with vinyl esters, such as vinyl acetate or vinyl propionate, acrylamide, methacrylamide and with ethylene, propylene or styrene. In those copolymeric acids in which one of the components has no acid function, the proportion thereof in the interest of sufficient water solubility is not more than 50 mole percent, preferably less than 30 mole percent. Copolymers of acrylic acid or methacrylic acid with maleic acid, as described in more detail in EP 25 551 B1, have proven to be particularly suitable. These are copolymers which contain 50 to 90% by weight of acrylic acid or methacrylic acid and 50 to 10% by weight of maleic acid. Copolymers in which 45 to 85% by weight of acrylic acid and 55 to 15% by weight of maleic acid are present are particularly preferred. The molecular weight of the homo- or copolymeric polycarboxylates is generally 2,000 to 150,000, preferably 5,000 to 100,000.
Handelsübliche Salze (co-)polymerer Carbonsäuren in pulvriger Form enthalten vielfach Feuchtigkeitsanteile von 5 - 15 Gew.-%. Dieser Wasseranteil wird in die Berechnung der Wasserbilanz eingebracht, bzw. die in die Granulierstufe eingebrachte Wassermenge kann um diesen Anteil reduziert werden. Rechnerisch ist der Anteil der Salze bei der Herstellung der Mittel bzw. bei der Zusammensetzung der fertigen Granulate auf wasserfreies Salz zu beziehen.Commercially available salts of (co) polymeric carboxylic acids in powder form often contain 5 to 15% by weight of moisture. This proportion of water is included in the calculation of the water balance, or the amount of water introduced into the pelletizing stage can be reduced by this proportion. In mathematical terms, the proportion of salts in the preparation of the compositions or in the composition of the finished granules is based on anhydrous salt.
Die Granulierung kann in üblichen Misch- und Granuliervorrichtungen diskontinuierlich oder kontinuierlich durchgeführt werden. Geeignet sind z. B. Granuliervorrichtungen, die aus einem horizontal angeordneten oder gegen die Horizontale geneigten, zylindrischen Behältern bestehen, in deren Längsachse eine mit Mischwerkzeugen und Förderschaufeln ausgerüstete Welle rotiert. Die Zuführung des Wassers kann durch in der Wandung oder an der hohlen Welle angebrachte Sprühdüsen erfolgen. Sofern kontinuierlich gearbeitet wird, können zwei hintereinander geschaltete Mischer verwendet werden, wobei im ersten Mischer die Herstellung des trocknen Vorgemisches und im zweiten Mischer die Granulierung unter Wasserzusatz erfolgt. Ein kontinuierliches Arbeiten ist auch in einem Mischer möglich, wobei in einer ersten Mischstrecke die Pulverströme vereinigt und homogenisiert werden und das Gemisch nach dem Weitertransport in einer nachfolgenden Mischstrecke mit Wasser behandelt und agglomeriert wird. Das Nachtrocknen kann durch Einleiten heißer Gase in einer dritten Mischstrecke z. B. einer Wirbelschicht, oder auch nach dem Austragen der Granulate aus dem Mischer beispielsweise in einer Rüttelstrecke, einem Freifalltrockner oder auch in dünner Schicht auf einem Transportband erfolgen. Abschließend werden Grob- und Feinanteile abgesiebt. Die Grobanteile werden gemahlen und dem Produkt zugemischt, Feinanteile bzw. Staub in die Granulation zurückgeführt.The granulation can be carried out batchwise or continuously in conventional mixing and granulating devices. Are suitable for. B. pelletizers, which consist of a horizontally arranged or inclined to the horizontal, cylindrical containers, in the longitudinal axis of which is equipped with a mixing tools and conveyor blades rotating shaft. The water can be supplied by spray nozzles mounted in the wall or on the hollow shaft. If work is carried out continuously, two consecutive mixers can be used, the dry premix being produced in the first mixer and the pelletizing taking place in the second mixer with the addition of water. Continuous work is also possible in a mixer, the powder streams being combined and homogenized in a first mixing section and the mixture being treated with water and agglomerating in a subsequent mixing section in a subsequent mixing section. The drying can be carried out by introducing hot gases in a third mixing section z. B. a fluidized bed, or after the granules have been discharged from the mixer, for example in a vibrating section, a free-fall dryer or in a thin layer on a conveyor belt. Finally coarse and fine particles are sieved. The coarse fractions are ground and mixed into the product, fine fractions or dust are returned to the granulation.
Die Granulate weisen ein Schüttgewicht von 750 - 1 000 g/l, meist ein solches von 800 - 950 g/l auf. Auf Grund ihrer dichten Packung und ihres geringen Porenvolumens ist ihr Aufnahmevermögen für flüssige bzw. pastenförmige Waschmittelbestandteile, insbesondere Nonionics, gegenüber spezifisch leichteren Trägerkörnern etwas vermindert, beträgt jedoch immer noch 15 bis maximal 20 Gew.-% ohne nennenswerte Beeinträchtigung der Rieselfähigkeit. Dieses angesichts der hohen Packungsdichte immer noch überraschende hohe Adsorptionsvermögen reicht für die üblichen Anwendungsgebiete, insbesondere für einen Einsatz als Mischungskomponente in Wasch-und Reinigungsmitteln, vollkommen aus.The granules have a bulk density of 750-1000 g / l, usually that of 800-950 g / l. Due to their tight packing and their small pore volume, their absorption capacity for liquid or pasty detergent components, especially nonionics, is somewhat reduced compared to specifically lighter carrier grains, but is still 15 to a maximum of 20% by weight without any appreciable impairment of the free-flowing properties. This In view of the high packing density, the surprisingly high adsorption capacity is completely sufficient for the usual fields of application, in particular for use as a mixture component in detergents and cleaning agents.
Überraschend ist ferner, daß die Granulate ungeachtet ihrer hohen Packungsdichte und ihres hohen Gehaltes an wasserunlöslichen Bestandteilen in kaltem Wasser schnell und vollständig zerfallen und in den Einspülvorrichtungen von Waschautomaten keine Rückstände hinterlassen, d. h. sie besitzen ein sehr gutes Einspülvermögen. Diese vorteilhafte Eigenschaft macht sich auch nach dem Imprägnieren mit Nonionics sowie im Gemisch mit anderen pulverförmigen Waschmittelkomponenten bemerkbar.It is also surprising that, regardless of their high packing density and their high content of water-insoluble constituents, the granules disintegrate quickly and completely in cold water and do not leave any residues in the induction devices of washing machines, i. H. they have a very good induction ability. This advantageous property is also noticeable after impregnation with Nonionics and in a mixture with other powder detergent components.
Die Granulate können mit beliebigen flüssigen oder pastenförmigen bzw. fettartigen Waschmittelbestandteilen imprägniert werden, die auf anderen Wegen nicht oder nur unter Wirkungsverlust in übliche pulverförmige bzw. granulare Wasch- oder Reinigungsmittel eingearbeitet werden können. Hierzu zählen Schauminhibitoren, insbesondere Paraffinkohlenwasserstoffe, Silikone, Silikonharze und von langkettigen Fettsäuren abgeleitete Bis-acyl-alkylendiamine sowie deren Gemische. Weitere adsorbierbare Wirkstoffe sind Fettsäurealkylolamide und kationische Weichmacher, wie langkettige Fettreste aufweisende quartäre Ammoniumsalze, ferner fettlösende Lösungsmittel, wie Terpene. Bevorzugt werden die Granulate als Trägerkörner für nichtionische Tenside eingesetzt. Dies ist ein weiterer Aspekt der Erfindung.The granules can be impregnated with any liquid or paste-like or fat-like detergent constituents which cannot be incorporated into conventional powdered or granular detergents or cleaning agents in other ways or only with a loss of activity. These include foam inhibitors, in particular paraffin hydrocarbons, silicones, silicone resins and bis-acylalkylenediamines derived from long-chain fatty acids, and mixtures thereof. Further adsorbable active ingredients are fatty acid alkylolamides and cationic plasticizers, such as quaternary ammonium salts containing long-chain fatty residues, and also fat-dissolving solvents, such as terpenes. The granules are preferably used as carrier grains for nonionic surfactants. This is another aspect of the invention.
Geeignete nichtionische Tenside sind Alkoxylierungsprodukte mit 10 bis 20 Kohlenstoffatomen im hydrophoben Rest und 3 bis 20 Glykolethergruppen. Hierzu zählen Ethoxylierungsprodukte von Alkoholen, vicinalen Diolen, Aminen, Thioalkoholen, Fettsäureamiden und Fettsäuren. Weiterhin sind Alkylphenolpolyglykolether mit 5 bis 12 C-Atomen im Alkylrest und 3 bis 10 Ethylenglykolethergruppen brauchbar. Ebenso kommen auch Blockpolymere aus Ethylenoxid und Propylenoxid, die unter der Bezeichnung Pluronics handelsüblich sind, in Betracht. Weiterhin können Alkylglycoside bzw. Alkylpolyglykoside sowie deren Gemische mit den genannten Ethoxylierungsprodukten verwendet werden.Suitable nonionic surfactants are alkoxylation products with 10 to 20 carbon atoms in the hydrophobic radical and 3 to 20 glycol ether groups. These include ethoxylation products of alcohols, vicinal diols, amines, thio alcohols, fatty acid amides and fatty acids. Alkylphenol polyglycol ethers with 5 to 12 carbon atoms in the alkyl radical and 3 to 10 ethylene glycol ether groups are also useful. Block polymers of ethylene oxide and propylene oxide, which are commercially available under the name Pluronics, are also suitable. Alkyl glycosides or alkyl polyglycosides and mixtures thereof with the ethoxylation products mentioned can also be used.
Bevorzugte Nonionics, die an dem Granulat adsorbiert sein können und mit diesem zusammen als rieselfähiges Gemisch vorliegen, leiten sich von Alkoholen mit 12 bis 18 C-Atomen ab, die gesättigt oder olefinisch ungesättigt, linear oder in 2-Stellung methylverzweigt (Oxo-Rest) sein können. Ihre Umsetzungsprodukte mit Ethylenoxid (EO) bzw. Propylenoxid (PO) sind wasserlösliche bzw. in Wasser dispergierbare Gemische von Verbindungen mit unterschiedlichem Alkoxylierungsgrad, wobei die im folgenden angegebene Anzahl der EO- bzw. PO-Gruppen einem statistischen Mittelwert entspricht.Preferred nonionics, which can be adsorbed on the granulate and together with it as a free-flowing mixture, are derived from alcohols with 12 to 18 carbon atoms which are saturated or olefinically unsaturated, linear or methyl-branched in the 2-position (oxo radical) could be. Their reaction products with ethylene oxide (EO) or propylene oxide (PO) are water-soluble or water-dispersible mixtures of compounds with different degrees of alkoxylation, the number of EO or PO groups given below corresponding to a statistical mean.
Beispiele für bevorzugte ethoxylierte Fettalkohole sind C₁₂₋₁₈-Cocosalkohole mit 3 bis 12 EO, C₁₆₋₁₈-Talgalkohol mit 4 bis 16 EO, Oleylalkohol mit 4 bis 12 EO sowie aus anderen nativen Fettalkoholgemischen erhältliche Ethoxylierungsprodukte entsprechender Ketten- und EO-Verteilung. Aus der Reihe der ethoxylierten Oxoalkohole sind beispielsweise solche der Zusammensetzung C₁₂₋₁₅ + 5 bis 10 EO und C₁₄₋C₁₅ + 6 bis 12 EO geeignet. Durch eine erhöhte Waschkraft sowohl gegenüber fettartigen und mineralischen Anschmutzungen zeichnen sich Gemische aus niedrig und hoch ethoxylierten Alkoholen aus, beispielsweise solche aus Talgalkohol + 3 bis 6 EO und Talgalkohol + 12 bis 16 EO oder C₁₃₋₁₅-Oxoalkohol + 5 EO und C₁₂₋₁₄-Oxoalkohol + 8 bis 12 EO. Weiterhin sind auch Ethoxylate geeignet, die EO-Gruppen und PO-Gruppen enthalten, z. B. C₁₂₋₁₈-Alkohole der Formel R-(PO)a-(EO)b bzw. R-(EO)b-(PO)c, worin a Zahlen von 1 bis 3, b solche von 5 bis 20 und c solche von 1 bis 10 (b größer als c) bedeuten.Examples of preferred ethoxylated fatty alcohols are C₁₂₋₁₈ coconut alcohols with 3 to 12 EO, C₁₆₋₁₈ tallow alcohol with 4 to 16 EO, oleyl alcohol with 4 to 12 EO and ethoxylation products of corresponding chain and EO distribution available from other native fatty alcohol mixtures. From the series of ethoxylated oxo alcohols, for example, those of the composition C₁₂₋₁₅ + 5 to 10 EO and C₁₄₋C₁₅ + 6 to 12 EO are suitable. Mixtures of low and highly ethoxylated alcohols are distinguished by an increased detergency against both greasy and mineral stains, for example those from tallow alcohol + 3 to 6 EO and tallow alcohol + 12 to 16 EO or C₁₃₋₁₅-oxo alcohol + 5 EO and C₁₂₋₁₄ oxo alcohol + 8 to 12 EO. Furthermore, ethoxylates are also suitable which contain EO groups and PO groups, e.g. B. C₁₂₋₁₈ alcohols of the formula R- (PO) a - (EO) b or R- (EO) b - (PO) c , wherein a numbers from 1 to 3, b such from 5 to 20 and c mean those from 1 to 10 (b greater than c).
Das Aufbringen der flüssigen, ggf. erwärmten Zusatzstoffe, insbesondere Nonionics auf das Granulat kann durch Zumischen, vorzugsweise Aufsprühen erfolgen, wobei das Trägermaterial zweckmäßigerweise durch geeignete Mischvorrichtungen in Bewegung gehalten wird. Eine weitere Nachbehandlung des körnigen Adsorbates ist nicht erforderlich. Allerdings kann ein mehrstündiges Ruhenlassen des Produktes bei hohen Gehalten an aufgebrachtem flüssigen Material zweckmäßig sein, da dessen Diffusion in das Korninnere einige Zeit in Anspruch nimmt. Die Behandlung der Granulate mit den flüssigen Zusatzstoffen führt zu einem weiteren Anstieg des Schüttgewichtes, das bis auf Werte von über 1 000 g/l ansteigen kann.The liquid, optionally heated, additives, in particular nonionics, can be applied to the granules by mixing, preferably spraying, the carrier material advantageously being kept in motion by suitable mixing devices. Further treatment of the granular adsorbate is not necessary. However, leaving the product to rest for several hours at high contents of applied liquid material can be expedient, since its diffusion into the interior of the grain takes some time. The treatment of the granules with the liquid additives leads to a further increase in the bulk density, which can rise to values of over 1,000 g / l.
Nach dem Aufbringen des flüssigen Zusatzstoffes können die Körner gegebenenfalls noch mit feinteiligen Pulvern bestäubt bzw. oberflächlich beschichtet werden. Hierdurch kann die bei hohen, 15 % übersteigenden Gehalten an Nonionics die Rieselfähigkeit verbessert und das Schüttgewicht geringfügig erhöht werden. Geeignete Puderungsmittel weisen eine Körngröße von 0,001 bis höchstens 0,1 mm, vorzugsweise von weniger als 0,05 mm auf und können in Anteilen von 0,03 bis 3, vorzugsweise 0,05 mm bis 2 Gew.-%, bezogen auf das mit Zusatzstoff beladene Adsorptionsmittel, angewendet werden. In Frage kommen z. b. feinpulvrige Zeolithe, Kieselsäureaerogel (Aerosil(R)), farblose oder farbige Pigmente, wie Titandioxid. Im allgemeinen ist eine solche Nachbehandlung jedoch überflüssig, zumal durch sie die Lösungseigenschaften nicht verbessert werden.After the liquid additive has been applied, the grains can optionally be dusted with finely divided powders or coated on the surface. As a result, the free-flowing properties can be improved and the bulk weight increased slightly, if the nonionics content exceeds 15%. Suitable powdering agents have a grain size of 0.001 to at most 0.1 mm, preferably less than 0.05 mm and can be present in proportions of 0.03 to 3, preferably 0.05 mm to 2% by weight, based on the Additive-laden adsorbents can be used. For example, finely powdered zeolites, silica airgel (Aerosil (R) ), colorless or colored pigments such as titanium dioxide are suitable. in the in general, however, such an aftertreatment is superfluous, especially since it does not improve the solution properties.
Die Waschmitteladditive können mit dem körnigen bzw. pulverförmigen Waschmittel, beispielsweise einem Turmsprühpulver sowie dessen Gemischen mit weiteren Pulverkomponenten, wie Persalze, Enzymgranulate, Bleichaktivatoren bzw. Entschäumer enthaltenden Granulaten, in bekannter Weise vereinigt und vermischt werden. Das hohe Schüttgewicht und das günstige Einspülverhalten der erfindungsgemäßen Additive überträgt sich auf diese komplexen Gemische. In der Praxis enthalten die zusammengemischten Waschmittel im allgemeinen 10 bis 40 Gew.-% des erfindungsgemäßen Additivs.The detergent additives can be combined and mixed in a known manner with the granular or pulverulent detergent, for example a tower spray powder and its mixtures with other powder components, such as persalts, enzyme granules, bleach activators or defoamers. The high bulk density and the favorable flushing behavior of the additives according to the invention are transferred to these complex mixtures. In practice, the detergents mixed together generally contain 10 to 40% by weight of the additive according to the invention.
Die erfindungsgemäßen Granulate weisen einen anderen Kornaufbau auf als solche, die nach konventionellen Granulierverfahren hergestellt werden. Dies läßt sich auch durch elektronenmikroskopische Aufnahmen nachweisen. Wird, wie bei konventionellen Granulierverfahren üblich, der pulverförmige Zeolith im Mischer vorgelegt und eine Lösung des (co-)polymeren Salzes aufgesprüht, so entstehen Granulate, die sich äußerlich nicht von den erfindungsgemäßen Produkten unterscheiden, außer das ihr Schüttgewicht deutlich verringert ist. Die mit dem Rasterelektronenmikroskop erhaltenen Abbildungen zeigen Schnitte durch zwei verschiedene Granulatkörner im Vergrößerungsmaßstab 1 : 2 500 (Abb. 1 und 2) bzw. 1 : 5 000 (Abb. 3 und 4). Beide Körner weisen die identische qualitative und quantitative Zusammensetzung entsprechend den Angaben des Beispiels 1 auf. Die Abbildungen 1 und 3 zeigen ein Korn, bei dessen Herstellung der sprühgetrocknete Zeolith im Mischer mit einer 25 Gew.-%igen wäßrigen Lösung des copolymeren Salzes besprüht, granuliert und anschließend getrocknet wurde. Die Abbildungen 2 und 4 zeigen den Kornaufbau des nach den Angaben des Beispiels 1 hergestellten Produktes. Die Anordnung der kubischen Zeolithteilchen in Abbildung 1 und 3 ist völlig regellos. Große Poren wechseln mit stark verklebten, unregelmäßig aufgebauten Aggregaten. In Abbildung 2 und 4 sind die Zeolithwürfel wesentlich dichter und gleichförmiger gepackt. Einzelne Partien erinnern an einen Aufbau vergleichbar einem Straßenpflaster bzw. einem Mauerwerk. Auch die Porengröße ist deutlich verringert.The granules according to the invention have a different grain structure than those which are produced by conventional granulation processes. This can also be demonstrated by electron micrographs. If, as is customary in conventional granulation processes, the powdery zeolite is placed in the mixer and a solution of the (co) polymeric salt is sprayed on, granules are formed which do not differ externally from the products according to the invention, except that their bulk density is significantly reduced. The images obtained with the scanning electron microscope show sections through two different granules on a magnification scale of 1: 2 500 (Figs. 1 and 2) and 1: 5 000 (Figs. 3 and 4). Both grains have the same qualitative and quantitative composition as in Example 1. Figures 1 and 3 show a grain, in the production of which the spray-dried zeolite was sprayed in a mixer with a 25% strength by weight aqueous solution of the copolymeric salt, granulated and then dried. Figures 2 and 4 show the grain structure of the according to the information from Example 1 manufactured product. The arrangement of the cubic zeolite particles in Figures 1 and 3 is completely random. Large pores change with strongly glued, irregularly structured aggregates. In Figures 2 and 4, the zeolite cubes are packed much denser and more uniformly. Individual parts are reminiscent of a structure comparable to a pavement or a brickwork. The pore size is also significantly reduced.
Die Granulierung erfolgte in einem Mischgranulator, bestehend aus einem horizontal angeordneten zylindrischen Mischer mit einer in der Mittelachse rotierenden, mit Mischorganen bestückten Drehwelle (Bauart Lödige) mit einem Fassungsvermögen von 130 Litern und einer daran angeschlossenen, mit einer Drehzahl von 1200 bis 1500 Upm betriebenen Messermühle. In dem Mischgranulator wurden 69,5 Gew.-teile eines synthetischen, feinkristallinen, sprühgetrockneten Zeoliths vom Typ NaA, enthaltend 20 Gew.-% gebundenes Wasser, mit 8,8 Gew.-teilen pulverförmigem Natriumsalz eines Acrylsäure-maleinsäure-copolymers (Feuchtigkeitsgehalt 8 Gew.-%) zu einem homogenen Pulvergemisch vermischt. Das Copolymer (Sokalan(R) CP5 der Firma BASF, Ludwigshafen) wies ein Molekulargewicht von ca. 70 000 auf. Nach dem Mischen, das ca. 20 sec in Anspruch nahm, wurden mittels Düsen 21,7 Gew.-teile Wasser im Verlauf von 90 sec eingesprüht und das Gemisch unter ständigem Mischen noch weitere 3 Minuten granuliert. Das den Mischer verlassende Granulat wurde in einer Wirbelschicht mit heißen, strömenden Trockengasen getrocknet. Das Endprodukt wies die folgende Zusammensetzung auf:
72,9 Gew.-% Zeolith (wasserfrei gerechnet)
9,3 Gew.-% Polymersalz (wasserfrei gerechnet)
17,8 Gew.-% Wasser
Das Wasser war praktisch vollständig an dem Zeolith gebunden, woraus sich ein Wassergehalt des Zeoliths von 19,7 Gew.-% errechnet. Nach Absieben von ca. 15 % Grobkorn ergab eine Siebanalyse die folgende Kornverteilung (angegeben ist die auf den Sieben verbleibende Menge in Gew.-%):
72.9% by weight of zeolite (calculated as anhydrous)
9.3% by weight polymer salt (calculated anhydrous)
17.8 wt% water
The water was practically completely bound to the zeolite, from which a water content of the zeolite of 19.7% by weight is calculated. After screening about 15% coarse grain, a sieve analysis showed the following grain distribution (the amount in% by weight remaining on the sieves is given):
Das Schüttgewicht des Granulates betrug 900 g/l.The bulk density of the granules was 900 g / l.
Das Granulat wurde in einem Sprühmischer mit einem auf 40 °C erwärmten, flüssigen, nichtionischen Tensid besprüht, bestehend aus einem mit 5 Mol EO umgesetzten Gemisch von Cocos- und Talgalkohol im Verhältnis 1 : 4. Nach einer Standzeit von 1 Stunde wiesen die Adsorbate die folgenden Schüttgewichte auf:
Die mit dem nichtionischen Tensid behandelten Granulate waren gut rieselfähig und wiesen ein einwandfreies Einspülvermögen auf und zwar sowohl als unverschnittenes Pulver wie auch vermischt mit einem pulverförmigen Haushaltsmittel im Verhältnis 1 : 4.The granules treated with the nonionic surfactant were free-flowing and had a perfect wash-in capacity, both as unblended powder and mixed with a powdery household detergent in a ratio of 1: 4.
Claims (7)
- A process for the production of granules containing finely crystalline zeolite, sodium or potassium salts of polymeric or copolymeric carboxylic acids and water, characterized in that (a) a homogeneous, powder-form mixture of zeolite and the salt of the (co)polymeric carboxylic acid is prepared in a first mixing step, (b) the mixture thus prepared is agglomerated in a second mixing and granulation step and (c) the agglomerate obtained is dried until free-flowing granules having an apparent density of 750 to 1,000 g/l are obtained.
- A process as claimed in claim 1, characterized in that the granules produced contain (based on anhydrous substance) 60 to 80% by weight zeolite, 2 to 15% by weight of the sodium salt of the (co)polymeric carboxylic acid and 14 to 25% by weight water, including the water bound to zeolite.
- A process as claimed in claim 1, characterized in that the granules produced contain (based on anhydrous substance) 62 to 75% by weight and more especially 65 to 70% by weight zeolite and 4 to 12% by weight and more especially 5 to 10% by weight sodium salt of (co)polymeric carboxylic acids.
- A process as claimed in claim 1 and claim 2 or 3, characterized in that 70 to 95 parts by weight of a spray-dried, finely powdered zeolite containing 15 to 25% by weight and preferably 18 to 22% by weight bound water, including water of constitution, and 3 to 12 parts by weight of a sodium salt of (co)polymeric acids are homogeneously mixed, the resulting mixture is agglomerated in the presence of 15 to 25 parts by weight water and the water introduced in the granulation step (b) is removed by subsequent drying to a residual content of less than 5 parts by weight and preferably less than 3 parts by weight.
- Granules obtainable by the process claimed in one or more of claims 1 to 4 impregnated with up to 20% by weight (based on adsorbate) of at least one liquid, paste-form or fatty detergent ingredient.
- Granules as claimed in claim 5, characterized in that the impregnating agent consists of nonionic surfactants.
- The use of the granules obtainable by the process claimed in one or more of claims 1 to 4 or the granules claimed in claim 5 or 6 as a powder component in detergents and cleaning preparations.
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
DE3838086 | 1988-11-10 | ||
DE3838086A DE3838086A1 (en) | 1988-11-10 | 1988-11-10 | METHOD FOR PRODUCING HIGH DENSITY GRANULES CONTAINING ZEOLITE |
Publications (2)
Publication Number | Publication Date |
---|---|
EP0368137A1 EP0368137A1 (en) | 1990-05-16 |
EP0368137B1 true EP0368137B1 (en) | 1994-01-05 |
Family
ID=6366852
Family Applications (2)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
EP89912426A Pending EP0442923A1 (en) | 1988-11-10 | 1989-11-02 | Process for producing high-density zeolite-containing granules |
EP89120266A Expired - Lifetime EP0368137B1 (en) | 1988-11-10 | 1989-11-02 | Method for the preparation of high-density zeolite granules |
Family Applications Before (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
EP89912426A Pending EP0442923A1 (en) | 1988-11-10 | 1989-11-02 | Process for producing high-density zeolite-containing granules |
Country Status (9)
Country | Link |
---|---|
EP (2) | EP0442923A1 (en) |
JP (1) | JPH04501730A (en) |
KR (1) | KR900701992A (en) |
DE (2) | DE3838086A1 (en) |
DK (1) | DK86891A (en) |
ES (1) | ES2047091T3 (en) |
PT (1) | PT92223B (en) |
TR (1) | TR24018A (en) |
WO (1) | WO1990005175A1 (en) |
Families Citing this family (18)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
GB8922179D0 (en) * | 1989-10-02 | 1989-11-15 | Rohm & Haas | Polymer-containing granulates |
US5108646A (en) * | 1990-10-26 | 1992-04-28 | The Procter & Gamble Company | Process for agglomerating aluminosilicate or layered silicate detergent builders |
DE4038609A1 (en) * | 1990-12-04 | 1992-06-11 | Henkel Kgaa | METHOD FOR PRODUCING ZEOLITE GRANULES |
DE4110510A1 (en) * | 1991-03-30 | 1992-10-01 | Henkel Kgaa | LOW-ALKALINE, CHLORINE AND PHOSPHATE-FREE MACHINE DISTRIBUTORS IN THE FORM OF HEAVY-DENTAL POWDERS AND GRANULES |
DE4125330A1 (en) * | 1991-07-31 | 1993-02-04 | Henkel Kgaa | METHOD FOR PRODUCING ZEOLITE GRANULES |
DE4137470A1 (en) * | 1991-11-14 | 1993-05-19 | Henkel Kgaa | METHOD FOR PRODUCING LOW-ALKALINE, ACTIVE-CHLORINE AND PHOSPHATE-FREE MACHINE DISPERSIVE AGENTS IN THE FORM OF HEAVY GRANULES |
DE4216774A1 (en) * | 1992-05-21 | 1993-11-25 | Henkel Kgaa | Process for the continuous production of a granular washing and / or cleaning agent |
DE4228044A1 (en) * | 1992-08-24 | 1994-03-03 | Henkel Kgaa | Builder for detergents |
DE4229660A1 (en) * | 1992-09-04 | 1994-03-10 | Henkel Kgaa | Washing and cleaning agents with builders |
EP0639638A1 (en) * | 1993-08-18 | 1995-02-22 | The Procter & Gamble Company | Process for making detergent compositions |
DE19549411C2 (en) * | 1994-02-11 | 1999-05-12 | Degussa | Zeolite granulates with good re:dispersibility and high bulk density |
DE19504043C2 (en) * | 1994-02-11 | 1998-07-09 | Degussa | zeolite granules |
DE19515256A1 (en) * | 1995-04-26 | 1996-10-31 | Degussa | Zeolite granules, process for its preparation and use |
GB9820573D0 (en) * | 1998-09-22 | 1998-11-11 | Ind Zeolite Uk Ltd | Water absorbing composition |
DE19850100A1 (en) | 1998-10-29 | 2000-05-04 | Henkel Kgaa | Polymer granules through fluidized bed granulation |
DE102005025656A1 (en) | 2005-06-03 | 2006-12-07 | IPK-Institut für Pflanzengenetik und Kulturpflanzenforschung | Promoter for epidermis-specific, pathogen-inducible transgene expression in plants |
JP5705525B2 (en) * | 2010-12-16 | 2015-04-22 | 花王株式会社 | Zeolite composite particles |
EP3241889B1 (en) | 2016-05-03 | 2019-03-20 | The Procter and Gamble Company | Cleaning composition |
Family Cites Families (8)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
AT330930B (en) | 1973-04-13 | 1976-07-26 | Henkel & Cie Gmbh | PROCESS FOR THE PRODUCTION OF SOLID, SPILLABLE DETERGENTS OR CLEANING AGENTS WITH A CONTENT OF CALCIUM BINDING SUBSTANCES |
ZA774818B (en) * | 1976-08-17 | 1979-03-28 | Colgate Palmolive Co | Disintegrable detergent builder agglomerates |
EP0021267B1 (en) | 1979-06-18 | 1982-06-16 | PQ Corporation | Agglomerated zeolite ion exchanger |
DE2936984A1 (en) | 1979-09-13 | 1981-04-02 | Basf Ag, 6700 Ludwigshafen | USE OF (METH) ACRYLIC ACID-MALEIC ACID COPOLYMERISATES AS INCREDIBLE INHIBITORS IN DETERGENTS |
DE3316513A1 (en) | 1983-05-06 | 1984-11-08 | Joh. A. Benckiser Gmbh, 6700 Ludwigshafen | Abrasion resistant granular materials based on alkali metal aluminium silicate |
GB8329880D0 (en) | 1983-11-09 | 1983-12-14 | Unilever Plc | Particulate adjuncts |
DE3444960A1 (en) | 1984-12-10 | 1986-06-12 | Henkel KGaA, 4000 Düsseldorf | GRAINY ADSORPTION |
DE3614779A1 (en) | 1986-05-02 | 1987-11-05 | Henkel Kgaa | GRANULAR, PHOSPHATE-FREE WATER SOFTENER |
-
1988
- 1988-11-10 DE DE3838086A patent/DE3838086A1/en not_active Withdrawn
-
1989
- 1989-11-02 JP JP1511510A patent/JPH04501730A/en active Pending
- 1989-11-02 DE DE89120266T patent/DE58906639D1/en not_active Expired - Lifetime
- 1989-11-02 EP EP89912426A patent/EP0442923A1/en active Pending
- 1989-11-02 KR KR1019900701431A patent/KR900701992A/en not_active Application Discontinuation
- 1989-11-02 WO PCT/EP1989/001312 patent/WO1990005175A1/en not_active Application Discontinuation
- 1989-11-02 EP EP89120266A patent/EP0368137B1/en not_active Expired - Lifetime
- 1989-11-02 ES ES89120266T patent/ES2047091T3/en not_active Expired - Lifetime
- 1989-11-07 PT PT92223A patent/PT92223B/en not_active IP Right Cessation
- 1989-11-10 TR TR89/0954A patent/TR24018A/en unknown
-
1991
- 1991-05-08 DK DK086891A patent/DK86891A/en unknown
Also Published As
Publication number | Publication date |
---|---|
JPH04501730A (en) | 1992-03-26 |
DK86891A (en) | 1991-07-08 |
WO1990005175A1 (en) | 1990-05-17 |
DK86891D0 (en) | 1991-05-08 |
KR900701992A (en) | 1990-12-05 |
PT92223A (en) | 1990-05-31 |
EP0442923A1 (en) | 1991-08-28 |
DE3838086A1 (en) | 1990-05-17 |
EP0368137A1 (en) | 1990-05-16 |
ES2047091T3 (en) | 1994-02-16 |
DE58906639D1 (en) | 1994-02-17 |
TR24018A (en) | 1991-02-01 |
PT92223B (en) | 1995-07-06 |
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