EP0061599B1 - Granule of alkali metal aluminium silicate and pentasodium tripolyphosphate, and process for its preparation - Google Patents

Granule of alkali metal aluminium silicate and pentasodium tripolyphosphate, and process for its preparation Download PDF

Info

Publication number
EP0061599B1
EP0061599B1 EP82101655A EP82101655A EP0061599B1 EP 0061599 B1 EP0061599 B1 EP 0061599B1 EP 82101655 A EP82101655 A EP 82101655A EP 82101655 A EP82101655 A EP 82101655A EP 0061599 B1 EP0061599 B1 EP 0061599B1
Authority
EP
European Patent Office
Prior art keywords
weight
aluminosilicate
granulate
pentasodium triphosphate
water
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
Application number
EP82101655A
Other languages
German (de)
French (fr)
Other versions
EP0061599B2 (en
EP0061599A1 (en
Inventor
Alexander Dr. Maurer
Renate Adrian
Horst Dieter Dr. Wasel-Nielen
Günter Sorbe
Joachim Dr. Kandler
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
Hoechst AG
Original Assignee
Hoechst AG
Priority date (The priority date 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 date listed.)
Filing date
Publication date
Family has litigation
First worldwide family litigation filed litigation Critical https://patents.darts-ip.com/?family=6127993&utm_source=google_patent&utm_medium=platform_link&utm_campaign=public_patent_search&patent=EP0061599(B1) "Global patent litigation dataset” by Darts-ip is licensed under a Creative Commons Attribution 4.0 International License.
Application filed by Hoechst AG filed Critical Hoechst AG
Priority to AT82101655T priority Critical patent/ATE11792T1/en
Publication of EP0061599A1 publication Critical patent/EP0061599A1/en
Publication of EP0061599B1 publication Critical patent/EP0061599B1/en
Application granted granted Critical
Publication of EP0061599B2 publication Critical patent/EP0061599B2/en
Expired legal-status Critical Current

Links

Classifications

    • CCHEMISTRY; METALLURGY
    • C11ANIMAL OR VEGETABLE OILS, FATS, FATTY SUBSTANCES OR WAXES; FATTY ACIDS THEREFROM; DETERGENTS; CANDLES
    • C11DDETERGENT COMPOSITIONS; USE OF SINGLE SUBSTANCES AS DETERGENTS; SOAP OR SOAP-MAKING; RESIN SOAPS; RECOVERY OF GLYCEROL
    • C11D3/00Other compounding ingredients of detergent compositions covered in group C11D1/00
    • C11D3/02Inorganic compounds ; Elemental compounds
    • C11D3/04Water-soluble compounds
    • C11D3/06Phosphates, including polyphosphates
    • CCHEMISTRY; METALLURGY
    • C11ANIMAL OR VEGETABLE OILS, FATS, FATTY SUBSTANCES OR WAXES; FATTY ACIDS THEREFROM; DETERGENTS; CANDLES
    • C11DDETERGENT COMPOSITIONS; USE OF SINGLE SUBSTANCES AS DETERGENTS; SOAP OR SOAP-MAKING; RESIN SOAPS; RECOVERY OF GLYCEROL
    • C11D3/00Other compounding ingredients of detergent compositions covered in group C11D1/00
    • C11D3/02Inorganic compounds ; Elemental compounds
    • C11D3/12Water-insoluble compounds
    • C11D3/124Silicon containing, e.g. silica, silex, quartz or glass beads
    • C11D3/1246Silicates, e.g. diatomaceous earth
    • C11D3/128Aluminium silicates, e.g. zeolites

Definitions

  • Alkaline alumosilicates especially crystalline or amorphous zeolites, are becoming increasingly important as detergent builders.
  • these builders only reach in combination with other complexing agents for divalent cations such as. B. pentasodium triphosphate, NTPP for short, optimal washing properties.
  • B. pentasodium triphosphate, NTPP for short, optimal washing properties.
  • alkali alumosilicates are fine powder, there is great interest in non-dusting, free-flowing granules which contain both alkali alumosilicates and NTPP. These can then be added dry to the other detergent components without dust formation, hydrolysis of the triphosphate also being avoided.
  • DE-A-2 714 604 describes a granulate consisting of ion-exchanging alkali alumosilicate, a highly polymeric phosphate with a P 2 0 s content of 64-69%, and pentasodium triphosphate.
  • the high polymer phosphate is added to the granulation mixture in powder form in the form of alkali salts and in an amount of at least 5% by weight, based on the alkali alumosilicate used. The mixture is then granulated in the presence of water.
  • This method has the disadvantage that the water is bound by the NTPP so quickly that it is no longer able to dissolve enough polymer phosphate for better granulation. Therefore, either larger amounts of polymer phosphate and longer vellwell times are required, or more water has to be added, which means that the granules have to be subsequently dried at 50 ° C.
  • DE-A-2 756 732 describes a granulate which likewise consists of alkali alumosilicate and a partially or fully hydrated alkali polyphosphate.
  • This granulate is produced by spraying water in fine mists onto the powder mixture of the granulate components, with a maximum of 10% of the total amount of water being allowed to be added per minute, since otherwise too large granulate particles are obtained in addition to a high dust content. This process therefore harbors the danger of producing granules with a very broad grain spectrum which still have to be sieved afterwards.
  • DE-A-2 822 231 describes granules of hydrated pentasodium triphosphate and water-insoluble aluminosilicate ion exchange material. This is also produced by spraying water onto the powder mixture, the total amount of water used being at least that required to achieve a minimum hydrate water content of about 10% by weight in the sodium tripolyphosphate and a water content in the aluminosilicate ion exchange material of 1.8 to 13.5 mol water per mol aluminosilicate .
  • the strength of the granulate particles obtained in this way can still be improved, as will be shown below with reference to the invention.
  • the proportion of the partially or fully hydrated pentasodium triphosphate is 30-70% by weight and the proportion of the ammonium polyphosphate is 0.03 to 1.6% by weight. At least 10% by weight of the pentasodium triphosphate is present here tes as hexahydrate and at least 30 wt .-% of the aluminosilicate as hydrate with a maximum of 13.5 moles of water per mole of aluminosilicate.
  • spraying is preferably carried out on an intimate powdery mixture of 1 to 99% by weight of an anhydrous or optionally at most 5% by weight water-containing pentasodium triphosphate and 99 to 1% by weight of a powdered, anhydrous or optionally bound water containing aluminosilicate ion exchange material of the general formula in which Kat, Me, w, x and y have the meaning given, with vigorous mixing, an aqueous 0.5-20% by weight solution in a fine mist and granulates the mixture with partial or complete hydration of the pentasodium triphosphate or Aluminum silicate exchange material.
  • the powdery mixture can consist of 30 to 70% by weight of the pentasodium triphosphate and 70 to 30% by weight of the aluminosilicate, the latter, for example, a zeolite of the formula can be.
  • the pentasodium triphosphate is present as hexahydrate and at least 30% by weight of the aluminosilicate is present as a hydrate with at most 13.5 mol of water per mol of aluminosilicate in the finished granulate.
  • the mixture is generally sprayed with an aqueous 1-10% by weight solution of ammonium polyphosphate.
  • Products of the aforementioned formula composition are to be used as the aluminosilicate ion exchange material.
  • Zeolites such as e.g. Zeolite A. Because of their use as detergent builders, they are in very fine-particle form, for example with an average particle diameter of 3-5 ⁇ m.
  • the P 2 0 5 content of the ammonium polyphosphate used for the granulation is more than 69%, polyphosphates with a P 2 0 5 content of over 71% being preferred.
  • the process according to the invention can be carried out, for example, by first mixing the pentasodium triphosphate with the aluminosilicate material in a mixer and then spraying the aqueous ammonium polyphosphate solution onto the mixture via a nozzle.
  • the spraying can also be carried out, for example, in a rotary tube or on a granulating plate onto the premixed material. It is important to ensure that no more granulating liquid is sprayed on than is necessary for the complete hydration of the sodium triphosphate contained in the mixture.
  • a granulate produced in this way is not dusty, abrasion-resistant and stable in storage. It meets the requirements for further processing in detergents by dry admixing.
  • Example 2 The procedure was as in Example 1, but using a 4% aqueous APP solution.
  • the mixed granules obtained from sodium triphosphate and zeolite had the following properties:

Abstract

The disclosure relates to a granulate with a particle size essentially of about 0.2 to 2 mm consisting of (a) about 2 to 95 weight % of a partially or completely hydrated pentasodium tripolyphosphate, (b) less than 3 weight % of an ammonium polyphosphate and the balance (c) being in the form of a water-insoluble aluminum silicate ion exchanging material. The granulate can be used in detergents.

Description

Alkalialumosilicate, besonders kristalline oder amorphe Zeolithe, gewinnen als Waschmittelgerüststoffe zunehmend an Bedeutung. Diese Gerüststoffe erreichen allerdings erst in Kombination mit anderen Komplexbildnern für zweiwertige Kationen wie z. B. Pentanatriumtriphosphat, kurz NTPP genannt, optimale Wascheigenschaften. Da Alkalialumosilicate feinpulvrig sind, besteht ein großes Interesse an nicht staubenden, gut rieselfähigen Granulaten, die sowohl Alkalialumosilicate als auch NTPP enthalten. Diese können dann den übrigen Waschmittelkomponenten ohne Staubbildung trokken zugemischt werden, wobei auch eine Hydrolyse des Triphosphats vermieden wird.Alkaline alumosilicates, especially crystalline or amorphous zeolites, are becoming increasingly important as detergent builders. However, these builders only reach in combination with other complexing agents for divalent cations such as. B. pentasodium triphosphate, NTPP for short, optimal washing properties. Since alkali alumosilicates are fine powder, there is great interest in non-dusting, free-flowing granules which contain both alkali alumosilicates and NTPP. These can then be added dry to the other detergent components without dust formation, hydrolysis of the triphosphate also being avoided.

Es wurden bereits mehrfach Anstrengungen unternommen, Alkalialumosilicate, vor allem Zeolithe, zusammen mit Alkalipolyphosphaten zu granulieren. So wird beispielsweise in der DE-A-2 714 604 ein Granulat beschrieben, das aus ionenaustauschendem Alkalialumosilicat, einem hochpolymeren Phosphat mit einem P20s-Gehalt von 64-69%, sowie Pentanatriumtriphosphat besteht. Das Hochpolymere Phosphat wird hierbei in Form von Alkalisalzen und in einer Menge von mindestens 5 Gew.-%, bezogen auf das eingesetzte Alkalialumosilicat, in Pulverform dem Granuliergemisch zugesetzt. Anschließend wird das Gemisch in Gegenwart von Wasser granuliert. Dieses Verfahren hat den Nachteil, daß das Wasser vom NTPP so schnell gebunden wird, daß es nicht mehr in der Lage ist, genügend Polymerphosphat zur besseren Granulierung zu lösen. Daher benötigt man entweder größere Mengen Polymerphosphat und längere Veiwellzeiten, oder man muß mehr Wasser zusetzen, was dazu führt, daß man das Granulat anschließend bei 50° C nachtrocknen muß.Efforts have been made several times to granulate alkali alumosilicates, especially zeolites, together with alkali polyphosphates. For example, DE-A-2 714 604 describes a granulate consisting of ion-exchanging alkali alumosilicate, a highly polymeric phosphate with a P 2 0 s content of 64-69%, and pentasodium triphosphate. The high polymer phosphate is added to the granulation mixture in powder form in the form of alkali salts and in an amount of at least 5% by weight, based on the alkali alumosilicate used. The mixture is then granulated in the presence of water. This method has the disadvantage that the water is bound by the NTPP so quickly that it is no longer able to dissolve enough polymer phosphate for better granulation. Therefore, either larger amounts of polymer phosphate and longer vellwell times are required, or more water has to be added, which means that the granules have to be subsequently dried at 50 ° C.

In der DE-A-2 756 732 ist ein Granulat beschrieben, das ebenfalls aus Alkalialumosilicat und einem teilweise oder vollkommen hydratisierten Alkalipolyphosphat besteht. Die Herstellung dieses Granulats erfolgt durch Aufsprühen von Wasser in feinen Nebeln auf das Pulvergemisch der Granulatkomponenten, wobei pro Minute höchstens 10% der Gesamtwassermenge zugegeben werden dürfen, da sonst zu große Granulatteilchen neben hohem Staubanteil erhalten werden. Dieses Verfahren birgt somit die Gefahr, daß ein Granulat mit sehr breitem Kornspektrum erzeugt wird, das nachträglich noch gesiebt werden muß.DE-A-2 756 732 describes a granulate which likewise consists of alkali alumosilicate and a partially or fully hydrated alkali polyphosphate. This granulate is produced by spraying water in fine mists onto the powder mixture of the granulate components, with a maximum of 10% of the total amount of water being allowed to be added per minute, since otherwise too large granulate particles are obtained in addition to a high dust content. This process therefore harbors the danger of producing granules with a very broad grain spectrum which still have to be sieved afterwards.

Weiterhin ist es gemäß DE-A-2 736 903 bekannt, Zeolithteilchen mit Wasser undStärke als Bindemittel zu granulieren. Dabei können auch bestimmte Anteile von NTPP mitgranuliert werden. Die Verwendung von Stärke oder ähnlichen Stoffen als Bindemittel bedeutet jedoch, daß eine für den Waschprozeß nutzlose Substanz in das Granulat eingebracht wird.Furthermore, according to DE-A-2 736 903 it is known to granulate zeolite particles with water and starch as a binder. Certain portions of NTPP can also be granulated. However, the use of starch or similar substances as binders means that a substance useless for the washing process is introduced into the granules.

Schließlich wird in der DE-A-2 822 231 ein Granulat aus hydratisiertem Pentanatriumtriphosphat und wasserunlöslichem Alumosilicationenaustauschmaterial beschrieben. Dieses wird ebenfalls durch Aufsprühen von Wasser auf das Pulvergemisch hergestellt, wobei die eingesetzte Gesamtwassermenge zumindest der zur Erzielung eines Mindesthydratwassergehaltes von etwa 10 Gew.-% im Natriumtripolyphosphat sowie eines Wassergehaltes im Alumosilicationenaustauschmaterial von 1,8 bis 13,5 Mol Wasser pro Mol Alumosilicat entspricht. Die Festigkeit der hierbei erhaltenen Granulatteilchen läßt sich noch, wie im folgenden anhand der Erfindung gezeigt wird, verbessern.Finally, DE-A-2 822 231 describes granules of hydrated pentasodium triphosphate and water-insoluble aluminosilicate ion exchange material. This is also produced by spraying water onto the powder mixture, the total amount of water used being at least that required to achieve a minimum hydrate water content of about 10% by weight in the sodium tripolyphosphate and a water content in the aluminosilicate ion exchange material of 1.8 to 13.5 mol water per mol aluminosilicate . The strength of the granulate particles obtained in this way can still be improved, as will be shown below with reference to the invention.

Es wurde nunmehr gefunden, daß die Nachteile der bekannten Granulate und deren Herstellungsverfahren vermieden werden können, wenn man zur Granulierung eines wasserunlöslichen Alumosilicats und Pentanatriumtriphosphats eine verdünnte wäßrige Lösung eines Ammoniumpolyphosphates als Bindemittel einsetzt.It has now been found that the disadvantages of the known granules and their production processes can be avoided if a dilute aqueous solution of an ammonium polyphosphate is used as a binder for granulating a water-insoluble aluminosilicate and pentasodium triphosphate.

Somit betrifft der Gegenstand der Erfindung ein Granulat, das ein teilweise oder vollkommen hydratisiertes Pentanatriumtriphosphat sowie wasserunlösliches Alumosilicationenaustauschmaterial der allgemeinen Formel (11)

Figure imgb0001
enthält, in welcher Kat ein mit Calcium austauschbares Kation der Wertigkeit w, x eine Zahl von 0,7-1,5, Me Bor oder Aluminium, y eine Zahl von 0,8-6 und z eine Zahl von 1,8-13,5 ist, wobei sich dieses Granulat dadurch auszeichnet, daß es

  • a) eine Teilchengröße von 0,2-2 mm aufweist;
  • b) 2-95 Gew.-% des Pentanatriumtriphosphates;
  • c) weniger als 3 Gew.-% eines Ammoniumpolyphosphates der allgemeinen Formel (I)
    Figure imgb0002
    in welcher n einen ganzzahligen Durchschnittswert von 100 bis 1000, m eine ganze Zahl bis maximal n + bedeutet und m/n einen Wert von etwa 1 darstellt und als Rest
  • d) das genannte Alumosilicationenaustauschmaterial enthält.
The subject matter of the invention thus relates to a granulate which comprises a partially or completely hydrated pentasodium triphosphate and water-insoluble aluminosilicate ion exchange material of the general formula (11)
Figure imgb0001
contains in which cat contains a calcium exchangeable cation of valence w, x a number of 0.7-1.5, Me boron or aluminum, y a number of 0.8-6 and z a number of 1.8-13 , 5, whereby this granulate is characterized in that it
  • a) has a particle size of 0.2-2 mm;
  • b) 2-95% by weight of the pentasodium triphosphate;
  • c) less than 3% by weight of an ammonium polyphosphate of the general formula (I)
    Figure imgb0002
    in which n is an integer average value from 100 to 1000, m is an integer up to a maximum of n + and m / n is a value of approximately 1 and the remainder
  • d) contains said aluminosilicate ion exchange material.

Gemäß einer bevorzugten Granulatkomposition beträgt der Anteil des teilweise oder vollkommen hydratisierten Pentanatriumtriphosphates 30-70 Gew.-% und der Anteil des Ammoniumpolyphosphates 0,03 bis 1,6 Gew.-%. Hierbei liegen mindestens 10 Gew.-% des Pentanatriumtriphosphates als Hexahydrat und mindestens 30 Gew.-% des Alumosilicates als Hydrat mit höchstens 13,5 Mol Wasser pro Mol Alumosilicat vor. Zur Herstellung des erfindungsgemäßen Granulats sprüht man vorzugsweise auf ein inniges pulverförmiges Gemisch aus 1 bis 99 Gew.-% eines wasserfreien oder gegebenenfalls höchstens 5 Gew.-% Wasser enthaltenden Pentanatriumtriphosphates und 99 bis 1 Gew.-% eines pulverförmigen, wasserfreien oder gegebenenfalls gebundenes Wasser enthaltenden Alumosilicationenaustauschmaterials der allgemeinen Formel

Figure imgb0003
in welcher Kat, Me, w, x und y die genannte Bedeutung haben, unter intensivem Durchmischen eine wäßrige, 0,5-20gewichts-%ige Lösung in einen feinen Nebel auf und granuliert das Gemisch unter teilweise oder vollkommener Hydratisierung des Pentanatriumtriphosphates bzw. des Alumosilicationenaustauschmaterials.According to a preferred granulate composition, the proportion of the partially or fully hydrated pentasodium triphosphate is 30-70% by weight and the proportion of the ammonium polyphosphate is 0.03 to 1.6% by weight. At least 10% by weight of the pentasodium triphosphate is present here tes as hexahydrate and at least 30 wt .-% of the aluminosilicate as hydrate with a maximum of 13.5 moles of water per mole of aluminosilicate. To produce the granules according to the invention, spraying is preferably carried out on an intimate powdery mixture of 1 to 99% by weight of an anhydrous or optionally at most 5% by weight water-containing pentasodium triphosphate and 99 to 1% by weight of a powdered, anhydrous or optionally bound water containing aluminosilicate ion exchange material of the general formula
Figure imgb0003
in which Kat, Me, w, x and y have the meaning given, with vigorous mixing, an aqueous 0.5-20% by weight solution in a fine mist and granulates the mixture with partial or complete hydration of the pentasodium triphosphate or Aluminum silicate exchange material.

Das pulverförmige Gemisch kann dabei aus 30 bis 70 Gew.-% des Pentanatriumtriphosphates und 70 bis 30 Gew.-% des Alumosilicates bestehen, wobei letzteres beispielsweise ein Zeolith der Formel

Figure imgb0004
sein kann.The powdery mixture can consist of 30 to 70% by weight of the pentasodium triphosphate and 70 to 30% by weight of the aluminosilicate, the latter, for example, a zeolite of the formula
Figure imgb0004
can be.

Es hat sich weiterhin als vorteilhaft erwiesen, wenn im fertigen Granulat mindestens 10 Gew.-% des Pentanatriumtriphosphates als Hexahydrat und mindestens 30 Gew.-% des Alumosilicates als Hydrat mit höchstens 13,5 Mol Wasser pro Mol Alumosilicat vorliegen. Das Besprühen des Gemisches erfolgt im allgemeinen mit einer wäßrigen 1-10gewichts-%igen Lösung von Ammoniumpolyphosphat.It has also proven to be advantageous if at least 10% by weight of the pentasodium triphosphate is present as hexahydrate and at least 30% by weight of the aluminosilicate is present as a hydrate with at most 13.5 mol of water per mol of aluminosilicate in the finished granulate. The mixture is generally sprayed with an aqueous 1-10% by weight solution of ammonium polyphosphate.

Im einzelnen ist zum Verfahren der Erfindung noch folgendes zu bemerken:

  • Als Natriumtriphosphat kann sowohl ein feingemahlenes Produkt, das beispielsweise maximal 2% einer Kornfraktion über 0,4 mm besitzt, als auch ein gröberes Produkt, dessen Anteil >0,15 mm mindestens 70% beträgt, eingesetzt werden. Die Verteilung der Modifikationen I und II im NTPP ist variabel, jedoch werden schneller hydratisierende Typen mit einem Gehalt an Modifikation 1 von 20-60% mit Vorteil eingesetzt.
In particular, the following should be noted regarding the method of the invention:
  • Sodium triphosphate can be either a finely ground product, which has, for example, a maximum of 2% of a grain fraction above 0.4 mm, or a coarser product, the proportion of which is> 0.15 mm at least 70%. The distribution of modifications I and II in the NTPP is variable, but faster hydrating types with a modification 1 content of 20-60% are used with advantage.

Als Alumosilicat-Ionenaustauschmaterial sind Produkte der erwähnten formelmäßigen Zusammensetzung zu verwenden. Bevorzugt eingesetzt werden Zeolithe, wie z.B. Zeolith A. Wegen ihrer Verwendung als Waschmittelgerüststoff liegen sie in sehr feinteiliger Form, beispielsweise mit einem mittleren Teilchendurchmesser von 3-5 µm, vor.Products of the aforementioned formula composition are to be used as the aluminosilicate ion exchange material. Zeolites, such as e.g. Zeolite A. Because of their use as detergent builders, they are in very fine-particle form, for example with an average particle diameter of 3-5 μm.

Der P205-Gehalt des zur Granulierung eingesetzten Ammoniumpolyphosphates beträgt mehr als 69%, wobei Polyphosphate mit einem P205-Gehalt von über 71 % bevorzugt werden.The P 2 0 5 content of the ammonium polyphosphate used for the granulation is more than 69%, polyphosphates with a P 2 0 5 content of over 71% being preferred.

Die Durchführung des erfindungsgemäßen Verfahrens kann beispielsweise derart erfolgen, daß man in einem Mischer das Pentanatriumtriphosphat mit dem Alumosilicatmaterial zunächst mischt und dann auf die Mischung über eine Düse die wäßrige Ammoniumpolyphosphatlösung aufsprüht. Das Aufsprühen kann auch beispielsweise in einem Drehrohr oder auf einem Granulierteller auf das vorgemischte Material erfolgen. Es ist darauf zu achten, daß man nicht mehr Granulierflüssigkeit aufsprüht als zur vollständigen Hydratation des im Gemisch enthaltenen Natriumtriphosphats notwendig ist. Ein derart hergestelltes Granulat ist nicht staubend, abriebfest und lagerstabil. Es erfüllt die Anforderungen, die für eine Weiterverarbeitung in Waschmitteln durch trockenes Zumischen gestellt werden.The process according to the invention can be carried out, for example, by first mixing the pentasodium triphosphate with the aluminosilicate material in a mixer and then spraying the aqueous ammonium polyphosphate solution onto the mixture via a nozzle. The spraying can also be carried out, for example, in a rotary tube or on a granulating plate onto the premixed material. It is important to ensure that no more granulating liquid is sprayed on than is necessary for the complete hydration of the sodium triphosphate contained in the mixture. A granulate produced in this way is not dusty, abrasion-resistant and stable in storage. It meets the requirements for further processing in detergents by dry admixing.

Beispiel 1example 1

In einem Freifallmischer wurden 67,5 kg wasserfreies Pentanatriumtriphosphat mit einem Phase-1-Gehalt von 50% und folgender Korngrößenverteilung:

  • > 1,6 mm = 0,7%,
  • > 0,8 mm = 3,8%,
  • > 0,4 mm = 20,5%,
  • > 0,2 mm = 67,8% und
  • >0,1 mm = 88,2%

sowie 67,5 kg eines Zeoliths (Zeolith A) mit einem Glühverlust von 19,8% und einer Korngrößenverteilung von 99% < 15 µm, 96%<10µm und 3% < 1 µm, während 20 min gemischt. Danach wurden 9 einer 8gewichts-%igen wäßrigen Lösung von Ammoniumpolyphosphat - im folgenden APP genannt - mit einer mittleren Kettenlänge von etwa 400 sowie einem P205-Gehalt von 72,4% im Verlauf von 3,5 Stunden unter ständigem weiteren Mischen aufgesprüht. Es wurde ein Mischgranulat aus Pentanatriumtriphosphat und dem Zeolith erhalten, das folgende Eigenschaften besaß:
Figure imgb0005
67.5 kg of anhydrous pentasodium triphosphate with a phase 1 content of 50% and the following particle size distribution were placed in a free-fall mixer:
  • > 1.6 mm = 0.7%,
  • > 0.8 mm = 3.8%,
  • > 0.4 mm = 20.5%,
  • > 0.2 mm = 67.8% and
  • > 0.1 mm = 88.2%

and 67.5 kg of a zeolite (zeolite A) with a loss on ignition of 19.8% and a particle size distribution of 99% <15 µm, 96% <10 µm and 3% <1 µm, mixed for 20 minutes. Then 9 of an 8% by weight aqueous solution of ammonium polyphosphate - hereinafter called APP - with an average chain length of about 400 and a P 2 0 5 content of 72.4% were sprayed on over the course of 3.5 hours with constant further mixing . A mixed granulate of pentasodium triphosphate and the zeolite was obtained, which had the following properties:
Figure imgb0005

Beispiel 2Example 2

Es wurde analog Beispiel 1 verfahren, wobei jedoch 41 APP-Lösung in 30 min aufgesprüht wurden. Das erhaltene Mischgranulat aus Pentanatriumtriphosphat und dem Zeolith besaß folgende Eigenschaften:

Figure imgb0006
The procedure was analogous to Example 1, but 41 APP solution were sprayed on in 30 min. The mixed granules obtained from pentasodium triphosphate and the zeolite had the following properties:
Figure imgb0006

Beispiel 3Example 3

Es wurde wie in Beispiel 1 verfahren, wobei jedoch eine 4%ige wäßrige APP-Lösung verwendet wurde. Das erhaltene Mischgranulat aus Natriumtriphosphat und Zeolith besaß folgende Eigenschaften:

Figure imgb0007
The procedure was as in Example 1, but using a 4% aqueous APP solution. The mixed granules obtained from sodium triphosphate and zeolite had the following properties:
Figure imgb0007

Beispiel 4Example 4

Es wurde wie in Beispiel 1 verfahren, wobei jedoch ein Natriumtriphosphat mit folgenden Eigenschaften als Ausgangsprodukt verwendet wurde: Glühverlust: 1,0 Gew.-%; Phase-1-Gehalt: 26%; Korngrößenverteilung:

  • >0,4 mm = 0,1%;
  • >0,2 mm = 3,8%;
  • >0,1 mm = 25,0%;
  • > 0,05 mm = 36,8%.
The procedure was as in Example 1, but using a sodium triphosphate with the following properties as the starting product: loss on ignition: 1.0% by weight; Phase 1 content: 26%; Grain size distribution:
  • > 0.4 mm = 0.1%;
  • > 0.2 mm = 3.8%;
  • > 0.1 mm = 25.0%;
  • > 0.05 mm = 36.8%.

Außerdem wurde eine 4gewichts-%ige wäßrige Lösung eines Ammoniumpolyphosphats mit einer mittleren Kettenlänge von 270 und einem P2O5-Gehalt von 72,4% eingesetzt. Das erhaltene Mischgranulat aus Natriumtriphosphat und dem Zeolith besaß folgende Eigenschaften:

Figure imgb0008
In addition, a 4% by weight aqueous solution of an ammonium polyphosphate with an average chain length of 270 and a P 2 O 5 content of 72.4% was used. The resulting mixed granules of sodium triphosphate and the zeolite had the following properties:
Figure imgb0008

Beispiel 5Example 5

Auf einem Granulierteller mit einem Durchmesser von 1 m wurden 20 kg eines Gemisches von 50 Gew.-% Natriumtriphosphat mit den in Beispiel 4 genannten Eigenschaften und 50 Gew.-% eines Zeoliths mit einem Glühverlust von 1,0 Gew.-% mit 41 APP-Lösung gemäß Beispiel 1 besprüht. Es wurde ein Mischgranulat aus Natriumtriphosphat und dem Zeolith mit folgenden Eigenschaften erhalten:

Figure imgb0009
20 kg of a mixture of 50% by weight sodium triphosphate with the properties mentioned in Example 4 and 50% by weight of a zeolite with a loss on ignition of 1.0% by weight using 41 APP were placed on a granulating plate with a diameter of 1 m Solution sprayed according to Example 1. A mixed granulate of sodium triphosphate and the zeolite was obtained with the following properties:
Figure imgb0009

Claims (9)

1. Granulate containing a partially or completely hydrated pentasodium triphosphate and a water-insoluble aluminosilicate ion exchanger of the general formula (II)
Figure imgb0014
in which cat is a calcium-exchangeable cation with the valency w, x is a number of 0.7-1.5, Me is boron or aluminium, y is a number of 0.8-6, and z is a number of 1.8--13.5, characterized in that it has
a) a particle size of 0.2-2 mm and contains,
b) 2-95 weight % of the pentasodium triphosphate,
c) less than 3 weight % of an ammonium polyphosphate of general formula (I)
Figure imgb0015
in which n stands for an integral average value of 100-1000, m stands for a whole number of at most n+2, and m/n stands for a value of about 1, and as balance,
d) the aluminosilicate ion exchanger mentioned.
2. Granulate as claimed in claim 1, containing the partially or completely hydrated pentasodium tripolyphosphate in a proportion of 0.03 to 1.6 weight %.
3. Granulate as claimed in claim 1 or 2, containing the ammonium polyphosphate in a proportion of 0.03-1.6 weight %.
4. Granulate as claimed in any of claims 1 to 3, wherein at least 10 weight % of the pentasodium triphosphate is present in the form of hexahydrate and at least 30 weight % of the aluminosilicate is present in the form of hydrate containing at most 13.5 mols water per mol aluminosilicate.
5. Process for making granulates as claimed in any of claims 1 to 4, which comprises spraying, with vigorous agitation, a fine mist of an aqueous 0.5 to 20 weight % solution of an ammonium polyphosphate of general formula (I) on to an intimate pulverulent blend of about 1 to 99 weight % of pentasodium triphosphate being anhydrous or containing at most 5 weight % of water, and about 99 to 1 weight % of a pulverulent alumosilicate ion exchanging material being anhydrous or having chemically combined water contained in it and corresponding to the following general formula
Figure imgb0016
in which cat, Me, w, x and y have the meanings given, and granulating the blend with partial or complete hydration of the pentasodium triphosphate and alumosilicate ion exchanger.
6. Process as claimed in claim 5, wherein the pulverulent blend consists of 30 to 70 weight % of pentasodium triphosphate and 70 to 30 weight % of alumosilicate.
7. Process as claimed in claim 5 or 6, wherein the aluminosilicate ion exchanger comprises zeolites, of the formula
Figure imgb0017
8. Process as claimed in any of claims 5-7, wherein the quantity of water necessary to effect the granulation is selected so as to obtain a final granulate containing at least 10 weight % of the pentasodium triphosphate as hexahydrate and at least 30 weight % of aluminosilicate as hydrate having at most 13.5 mols water per mol aluminosilicate contained therein.
9. Process as claimed in any of claims 5-8, wherein an aqueous 1 to 10 weight % solution of ammonium polyphosphate is sprayed on to the blend.
EP82101655A 1981-03-21 1982-03-04 Granule of alkali metal aluminium silicate and pentasodium tripolyphosphate, and process for its preparation Expired EP0061599B2 (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
AT82101655T ATE11792T1 (en) 1981-03-21 1982-03-04 ALKALI AUMOSILICATE AND PENTANATRIUM TRIPHOSPHATE GRANULES AND PROCESS FOR PRODUCTION THEREOF.

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
DE3111236A DE3111236A1 (en) 1981-03-21 1981-03-21 GRANULATE FROM ALKALIALUMINUM SILICATE AND PENTANATRIUM TRIPHOSPHATE AND METHOD FOR THE PRODUCTION THEREOF
DE3111236 1981-03-21

Publications (3)

Publication Number Publication Date
EP0061599A1 EP0061599A1 (en) 1982-10-06
EP0061599B1 true EP0061599B1 (en) 1985-02-13
EP0061599B2 EP0061599B2 (en) 1988-07-06

Family

ID=6127993

Family Applications (1)

Application Number Title Priority Date Filing Date
EP82101655A Expired EP0061599B2 (en) 1981-03-21 1982-03-04 Granule of alkali metal aluminium silicate and pentasodium tripolyphosphate, and process for its preparation

Country Status (5)

Country Link
US (1) US4386024A (en)
EP (1) EP0061599B2 (en)
AT (1) ATE11792T1 (en)
CA (1) CA1161416A (en)
DE (2) DE3111236A1 (en)

Families Citing this family (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
DE3208138A1 (en) * 1982-03-06 1983-09-08 Hoechst Ag, 6230 Frankfurt ALKALISILICATE AND ALKALIPOLYPHOSPHATE COGRANULATE AND METHOD FOR PRODUCING THE GRANULATE
US4711748A (en) * 1985-12-06 1987-12-08 Lever Brothers Company Preparation of bleach catalyst aggregates of manganese cation impregnated aluminosilicates by high velocity granulation
US4655782A (en) * 1985-12-06 1987-04-07 Lever Brothers Company Bleach composition of detergent base powder and agglomerated manganese-alluminosilicate catalyst having phosphate salt distributed therebetween
DE4009082A1 (en) * 1990-03-21 1991-09-26 Aquamot Ag METHOD FOR CLEANING INDUSTRIAL, AGRICULTURAL, OR PRIVATE WASTEWATER FROM YOUR AMMONIUM COMPOUNDS

Family Cites Families (8)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US2801978A (en) * 1956-11-02 1957-08-06 B T Babbitt Inc Ammonia-containing detergents
US4014806A (en) * 1973-12-07 1977-03-29 David Connor Novel organopolyphosphates in aqueous cleaning compositions
US4248911A (en) * 1976-12-02 1981-02-03 Colgate-Palmolive Company Concentrated heavy duty particulate laundry detergent
DE2714604C3 (en) * 1977-04-01 1985-04-25 Joh. A. Benckiser Gmbh, 6700 Ludwigshafen Granulate based on polymer phosphate and ion-exchanging alkali aluminosilicate
DE2744773C3 (en) * 1977-10-05 1986-08-21 Joh. A. Benckiser Gmbh, 6700 Ludwigshafen Granulate based on polymer phosphate and ion-exchanging alkali aluminosilicate
DE2751354A1 (en) * 1977-11-17 1979-05-23 Hoechst Ag PROCESS FOR THE PREPARATION OF MIXTURES FROM CRYSTALLINE ZEOLITE AND SODIUM TRIPHOSPHATE
DE2822231A1 (en) * 1978-05-22 1979-11-29 Hoechst Ag GRANULATES MADE FROM HYDRATED SODIUM TRIPOLYPHOSPHATE AND WATER-INSOLUBLE ALUMOSILICATION EXCHANGE MATERIAL
DE2829165A1 (en) * 1978-07-03 1980-01-17 Henkel Kgaa METHOD FOR PRODUCING ALUMOSILICATE GRANULES

Also Published As

Publication number Publication date
DE3262256D1 (en) 1985-03-28
EP0061599B2 (en) 1988-07-06
EP0061599A1 (en) 1982-10-06
CA1161416A (en) 1984-01-31
ATE11792T1 (en) 1985-02-15
DE3111236A1 (en) 1982-09-30
US4386024A (en) 1983-05-31

Similar Documents

Publication Publication Date Title
DE2549337C2 (en) Process for the production of detergent granules containing aluminosilicate
EP0017827B2 (en) Process for the preparation of metallic soaps
DE2221876C2 (en) Process for the production of coated granules and their use for dishwashing detergents
DE19608000B4 (en) Process for the production of granular sodium percarbonate
DE2806161B2 (en) Method of stabilizing anhydrous sodium metasilicate
EP0061599B1 (en) Granule of alkali metal aluminium silicate and pentasodium tripolyphosphate, and process for its preparation
CH641203A5 (en) METHOD FOR PRODUCING GRANULES.
EP0006618B1 (en) Use of aluminium silicate granules as cation exchangers
DE2501698C2 (en) Mixtures containing optical brighteners and processes for their preparation
DE2348926B2 (en) Fire extinguishing composition
EP0392400B1 (en) Process for the preparation of a finely divided cristalline type A zeolithe powder with predetermined gram size distribution
EP0048341B1 (en) Process for the preparation of granulate alkali di- or triphosphates
EP0072971B1 (en) Process for producing zeolite agglomerates
EP0088267B1 (en) Cogranulate from alkali silicate and alkali phosphate, and process for the preparation of the granulate
EP0057822B1 (en) Process for producing granulated alkali orthophosphates
EP0061600B1 (en) Process for the preparation of mixed granules of condensed phosphates and builders
DE3640541A1 (en) Granular detergent
EP0075250A2 (en) Process for the production of a granulated raw material for detergents
DE2822765B2 (en) Granulated raw material for the manufacture of detergents and process for their manufacture
DE2925137A1 (en) Granular detergent compsns. - contg. specified amts. of tri:poly:phosphate, water and other ingredients
AT311523B (en) Process for the production of non-baking mixtures of sodium tripolyphosphate hexahydrate and sodium nitrilotriacetate monobwz. Dihydrate
DE3139858C2 (en)
EP0249829A2 (en) Process for the preparation of sodium metasilicate agglomerate
DE3620009A1 (en) CLEANING AGENTS CONTAINING KOERNIG AGGLOMERED SODIUM METASILICATE, METHOD FOR THE PRODUCTION AND USE THEREOF
DE2021528C3 (en) Process for the production of non-baking mixtures of hydrated sodium tripolyphosphate and sodium nitrilotriacetate and the use of these mixtures as detergents, cleaning agents or dishwashing agents

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

AK Designated contracting states

Designated state(s): AT BE CH DE FR GB IT NL SE

17P Request for examination filed

Effective date: 19830204

ITF It: translation for a ep patent filed

Owner name: SOCIETA' ITALIANA BREVETTI S.P.A.

GRAA (expected) grant

Free format text: ORIGINAL CODE: 0009210

AK Designated contracting states

Designated state(s): AT BE CH DE FR GB IT LI NL SE

REF Corresponds to:

Ref document number: 11792

Country of ref document: AT

Date of ref document: 19850215

Kind code of ref document: T

REF Corresponds to:

Ref document number: 3262256

Country of ref document: DE

Date of ref document: 19850328

ET Fr: translation filed
PLBI Opposition filed

Free format text: ORIGINAL CODE: 0009260

26 Opposition filed

Opponent name: DEGUSSA AG, FRANKFURT - ZWEIGNIEDERLASSUNG WOLFGAN

Effective date: 19850509

NLR1 Nl: opposition has been filed with the epo

Opponent name: DEGUSSA AG

PGFP Annual fee paid to national office [announced via postgrant information from national office to epo]

Ref country code: AT

Payment date: 19870220

Year of fee payment: 6

PGFP Annual fee paid to national office [announced via postgrant information from national office to epo]

Ref country code: NL

Payment date: 19870331

Year of fee payment: 6

PUAH Patent maintained in amended form

Free format text: ORIGINAL CODE: 0009272

STAA Information on the status of an ep patent application or granted ep patent

Free format text: STATUS: PATENT MAINTAINED AS AMENDED

27A Patent maintained in amended form

Effective date: 19880706

AK Designated contracting states

Kind code of ref document: B2

Designated state(s): AT BE CH DE FR GB IT NL SE

NLR2 Nl: decision of opposition
ET3 Fr: translation filed ** decision concerning opposition
ITF It: translation for a ep patent filed

Owner name: SOCIETA' ITALIANA BREVETTI S.P.A.

NLR3 Nl: receipt of modified translations in the netherlands language after an opposition procedure
PG25 Lapsed in a contracting state [announced via postgrant information from national office to epo]

Ref country code: GB

Effective date: 19890304

Ref country code: AT

Effective date: 19890304

PG25 Lapsed in a contracting state [announced via postgrant information from national office to epo]

Ref country code: SE

Effective date: 19890305

PG25 Lapsed in a contracting state [announced via postgrant information from national office to epo]

Ref country code: LI

Effective date: 19890331

Ref country code: CH

Effective date: 19890331

Ref country code: BE

Effective date: 19890331

BERE Be: lapsed

Owner name: HOECHST A.G.

Effective date: 19890331

PG25 Lapsed in a contracting state [announced via postgrant information from national office to epo]

Ref country code: NL

Effective date: 19891001

GBPC Gb: european patent ceased through non-payment of renewal fee
NLV4 Nl: lapsed or anulled due to non-payment of the annual fee
PG25 Lapsed in a contracting state [announced via postgrant information from national office to epo]

Ref country code: FR

Free format text: LAPSE BECAUSE OF NON-PAYMENT OF DUE FEES

Effective date: 19891130

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: 19891201

REG Reference to a national code

Ref country code: FR

Ref legal event code: ST

EUG Se: european patent has lapsed

Ref document number: 82101655.7

Effective date: 19900124