EP0618960B1 - Bleach activators in granular form (ii) - Google Patents

Bleach activators in granular form (ii) Download PDF

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Publication number
EP0618960B1
EP0618960B1 EP93901014A EP93901014A EP0618960B1 EP 0618960 B1 EP0618960 B1 EP 0618960B1 EP 93901014 A EP93901014 A EP 93901014A EP 93901014 A EP93901014 A EP 93901014A EP 0618960 B1 EP0618960 B1 EP 0618960B1
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EP
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Prior art keywords
granules
weight
binder
bleach activator
mixtures
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EP93901014A
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German (de)
French (fr)
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EP0618960A1 (en
Inventor
Volker Bauer
Jochen Jacobs
Christiane Zeise
Uwe Fassbach
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Henkel AG and Co KGaA
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Henkel AG and Co KGaA
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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
    • C11D3/39Organic or inorganic per-compounds
    • 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
    • C11D3/39Organic or inorganic per-compounds
    • C11D3/3902Organic or inorganic per-compounds combined with specific additives
    • C11D3/3905Bleach activators or bleach catalysts
    • C11D3/3935Bleach activators or bleach catalysts granulated, coated or protected
    • 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
    • C11D3/39Organic or inorganic per-compounds
    • C11D3/3902Organic or inorganic per-compounds combined with specific additives
    • C11D3/3905Bleach activators or bleach catalysts
    • C11D3/3907Organic compounds

Definitions

  • the invention relates to new pourable and free-flowing granules which contain bleach activators for textile washing embedded in a binder phase as the main component, the binder phase containing surfactants which are solid at room temperature and moderately elevated temperatures.
  • the invention further relates to a method for producing these new bleach activator granules.
  • Inorganic peroxy compounds that dissolve in water releasing hydrogen peroxide have long been used as oxidizing agents for disinfection and bleaching purposes.
  • the oxidizing effect of these substances in dilute solutions depends strongly on the temperature.
  • With perborate in alkaline bleaching liquors sufficiently quick bleaching of soiled textiles can only be achieved at temperatures above 60 ° C.
  • the oxidation effect of the inorganic per-compounds can be improved by adding activators, for which numerous proposals have become known in the literature.
  • the addition of these activators can increase the bleaching effect of aqueous peroxide liquors to such an extent that they are already active in the temperature range from 30 to 60 ° C., ie. H. at temperatures required for washing delicate textiles.
  • these activators are highly sensitive to hydrolysis, especially in the presence of the alkalis which are generally customary in detergents.
  • the problems derived from this for the storage stability of the textile detergents are exacerbated by the fact that the activators are often poorly soluble in water, so that finely powdered materials with rapid dispersibility should be used. This very finely divided form allows due to increased surface area the increased hydrolysis of the activators during their storage.
  • the bleach activator component in the form of separately produced granules to be added to the dry washing or cleaning agent mixtures, the agglomerates of very fine bleaching agent particles being coated with auxiliaries.
  • a wide variety of organic and inorganic substances have been proposed as granulation aids and coating materials for such activator granules.
  • surfactant compounds from the classes of anionic, cationic and / or nonionic surfactants, polymeric materials or waxes which are solid at room temperature.
  • the object of the present invention was therefore to avoid the above-mentioned disadvantages of the previous granules, without giving up their advantages, in particular the high storage stability and the ease of manufacture.
  • the invention relates to a pourable and free-flowing granulate which contains bleach activators for textile washing as a finely dispersed solid phase as the main constituent, embedded in a practically anhydrous phase penetrating the granulate grain and serving as a binder, and which is obtained by extrusion of a practically water-free mixture of bleach activator, anionic surfactant, solubilizing aid and optionally further additives are produced, characterized in that the solubilization aid is selected from the group consisting of polyethylene glycol, polypropylene glycol, anionically modified polyethylene glycol on one or both hydroxyl groups, anionically modified polypropylene glycol on one or both hydroxyl groups, and mixtures of these compounds.
  • Another object of the invention is a process for the production of the granules, in which the finely divided bleach activator is premixed with the other components, the mixture of substances is homogenized at a preferably elevated temperature to form an extrudable mass and extruded in the form of a strand using increased pressure, the emerging strands, if appropriate after cooling, cuts into short pieces and rounds off these pieces if necessary and, if desired, classified according to size.
  • the mixture of anionic surfactant and solubilizing aid which serves as the binder is preferably selected so that this mixture only softens at temperatures above the highest usual storage temperatures, ie above temperatures of about 35 to 40 ° C.
  • the granulation then takes place in the temperature range above, and if temperature-sensitive bleach activators or granulate components are used, corresponding upper limit temperatures must be observed.
  • the working temperatures during the granulation are not above 90 ° C., in particular not above 80 ° C., whereby working temperatures in the range from about 45 to 75 ° C. may be particularly suitable.
  • the anionic surfactant component may be chosen as the larger proportion in the binder mixture. It is particularly preferred here to use corresponding anionic surfactant compounds which are solid at room temperature and granulate formation temperature and which can make up at least 55% by weight and up to 98% by weight of the binder mixture.
  • the anionic surfactant content is in the range from 60 to 95% by weight, in particular 60 to 85% by weight, based on the weight of the binder mixture. Based on the total weight of the granulate, the proportion is preferably 4 to 25% by weight, in particular 6 to 15% by weight.
  • Suitable solid anionic surfactants are the solid components known in detergent technology, in particular in the context of textile detergents, which belong in particular to the following classes of substances: alkyl sulfates, alkyl sulfonates, alkylarylsulfonates, sulfonated fatty acid esters and / or soaps.
  • Particularly suitable anionic surfactants are, for example, C 12 -C 18 fatty alcohol sulfates, which can be present individually or in a mixture, such as lauryl sulfate, myristyl sulfate and here in particular C 16 -C 18 tallow alcohol sulfate.
  • alkylbenzenesulfonates with 9 to 13 carbon atoms in the alkyl chain, in particular C 12 alkylbenzenesulfonate, wash-active salts of alpha-sulfonated fatty acid methyl esters and / or sodium soaps of fatty acids, in particular of fatty acids with 12 to 18 carbon atoms .
  • the salts of long-chain ester carboxylic acids such as those obtainable from fatty alcohols having 8 to 18 carbon atoms and di- or polycarboxylic acids, for example maleic anhydride or citric acid, may also be suitable.
  • the anionic surfactants are preferably used in the form of the sodium salts.
  • the use of unsaturated components and / or the use of potassium soaps can influence the plasticizability of the binder mixture at the elevated working temperatures.
  • the compounds used as solubilization aids according to the invention are polyethylene and / or polypropylene glycols or derivatives of these compounds.
  • the average molecular weight of these polymers is preferably in the range between about 200 and about 12,000.
  • Polyethylene glycols with an average molecular weight between 600 and 4,000 are particularly preferred.
  • the derivatives of the polyalkylene glycols which are suitable according to the invention are polymers which have one or both terminal hydroxyl groups are anionically modified.
  • the sulfates and / or in particular the disulfates of the abovementioned polyalkylene glycols are suitable.
  • the sulfosuccinates and / or disulfosuccinates of these polyalkylene glycols are also suitable.
  • anionic derivatives are preferably derived from polyglycols with average molecular weights between 600 and 6000, in particular from those with average molecular weights between 1000 and 4000.
  • the anionic derivatives can be present as salts of any cations, but are preferably used as alkali salts, in particular as sodium or potassium salts, and as salts of organic amines, for example triethanolamine.
  • Mixtures of the polyalkylene glycol ethers and their anionically modified derivatives are preferably also used in any mixing ratio.
  • a mixture of polyalkylene glycol and the sulfosuccinates and / or disulfosuccinates of the polyalkylene glycols is preferred.
  • a mixture of polyalkylene glycol and the corresponding sulfates and / or disulfates and a mixture of polyalkylene glycol, the corresponding sulfates and / or disulfates and the corresponding sulfosuccinates and / or disulfosuccinates are also suitable.
  • the proportion of the solubilization aid in the granulate is preferably 0.5 to 15% by weight, in particular 1 to 6% by weight.
  • mixtures of anionic surfactant and solubilizing aids are used as binders which are highly effective plasticizers at the working temperature of the granulation, so that the desired plasticized good quality can be set with limited amounts of the binder.
  • the amounts of binder are preferably below about 50% by weight of the total mixture, and the bleach activator is preferably present in this total mixture in amounts of about 70 to 95% by weight.
  • Particularly suitable activator contents can range from about 75 to 90% by weight on the entire granulate.
  • the rest of the granulate is formed by the binder or at least to a substantial extent by this surfactant binder.
  • the granules contain at least about 3% by weight, preferably at least about 5% by weight, of the binder mixture, based in each case on the entire granulate, binder amounts in the range from about 7 to 25% by weight being particularly preferred can.
  • bleach activators for per-compounds are 0- and / or N-acylated compounds such as pentaacetylglucose (PAG), pentapropionylglucose (PPG), tetraacetylethylenediamine (TAED), tetraacetylglycoluril (TAGUanol, triacetylamine) TAEA), acylated triazine derivatives such as 1,5-diacetyl-2,4-dioxohexahydro-1,3,5-triazine (DADHT), carboxylic anhydrides such as succinic, benzoic or phthalic anhydride, salts of mixed anhydrides such as sodium or magnesium diacetyl phosphate ( NADAP or MGD
  • the process according to the invention for producing the bleach activator granules is characterized in that the multicomponent mixture is first mixed as uniformly as possible in a suitable mixing device in the region of room temperature or only moderately elevated temperatures. All customary devices, for example of the Lödige ploughshare mixer type, are suitable as the mixing device. This premix is then fed to the homogenization and extrusion stage.
  • a processing device has proven to be particularly suitable for carrying out the method according to the invention. This is the extrusion by means of a pellet press.
  • the temperature of the material in the working space of the pellet press can be set to predetermined values by means of this temperable pan, the aforementioned temperature range up to a maximum of 90 ° C. and preferably from 45 to 70 ° C. being selected here.
  • the cut granulate is subjected to shock cooling. Air or cooled air can be used as the cooling medium. Additionally or alternatively, the primarily extruded and cut granulate can be superficially loaded with particulate solids. Examples include powdered zeolites, especially detergent grade zeolite NaA, talc, silica and the like.
  • auxiliaries or additives may be desirable or expedient to incorporate further auxiliaries or additives into the granulate in addition to the finely divided solid bleach activators and the binder.
  • the proportion of these additives is preferably not more than 10% by weight, based on the granules.
  • Particularly noteworthy in this context are finely divided, readily soluble alkali salts of inorganic or organic acids.
  • the addition of these substances can in individual cases further accelerate the release of the activator when the granules are introduced into water.
  • Particularly suitable salts are sodium carbonate, sodium sulfate and sodium citrate.
  • the proportion of these salts in the granules is preferably not more than 10% by weight, based on the total weight of the granules, in particular it is between about 0.5% by weight and about 5% by weight.
  • additives which may be used are, for example, dyes as are customary in the detergent sector. To incorporate these substances, it may be appropriate to suspend or dissolve them in liquid granulate components before they are mixed in. Preferred dyes are pigment dyes, such as copper phthalocyanine dyes. For better distribution of the dye in the granules, it may be advantageous to disperse the dye in small amounts of water before the addition.
  • the amount of water should not be more than 1% by weight, preferably not more than 0.5% by weight, based on the total weight of the granules. Examples of other suitable auxiliaries are disintegrants and lubricants.
  • compression ratios can be set such that the finished granules have bulk densities of at least 500 g / l.
  • Bulk weights in the range up to 1000 g / l are particularly suitable, bulk densities in the range 600 to 900 g / l being preferred.
  • Preferred granules are either cylindrical or spherical.
  • the additional rounding of the cylindrical shapes can expediently take place immediately after cutting to length on the still sufficiently warm granulate.
  • Auxiliary devices suitable for rounding off are known, for example the Marumerizers used for this purpose.
  • the grain size of the granules is regulated in a manner known per se and is expediently set in the range from 0.7 to 3 mm.
  • the granules can be cut to the desired grain length of 0.7 to 3 mm or beyond, for example to a grain length of 5 mm.
  • These cylindrical granules with lengths above 3 mm are then broken to a predetermined length and rounded if necessary so that a length of 3 mm is not exceeded.
  • Cylindrical granules preferably have a length of up to 2 mm, while additionally rounded, preferably spherical granules have a particle diameter in the range from 0.4 mm to 1.6 mm.
  • the respective constituents were mixed intensively for one minute in a ploughshare mixer (Lödige, Germany) in the mixing ratios shown in the table.
  • the premix obtained in this way was then fed continuously to a ring die press (pellet press, embodiment according to DE 38 16 842, Schlüter, Germany), the temperature-controlled roller (press roll) of which was heated to 50.degree.
  • a ring die press pellet press, embodiment according to DE 38 16 842, Schlüter, Germany
  • the temperature-controlled roller press roll of which was heated to 50.degree.
  • the diameter of the press channels with which the ring die was penetrated was 1.2 mm.
  • the distance between the press roller and the ring die was 1.5 mm.
  • the emerging strand was cut to a length of 1.5 mm by a knife attached to the outside of the ring die.
  • the bulk weights of the granules were between 630 and 700 g / l.
  • the cut-to-length granules were then rounded off in a Marumerizer-type rounding machine.
  • the proportion of good grain (sieve fraction between 0.4 and 1.6 mm) of the granules decreased only slightly.

Abstract

The description relates to a pourable granulate, the main constituent of which are bleach activators for washing textiles in the form of a finely dispersed solid phase embedded in a virtually waterless phase penetrating the granulate grain and acting as a binder, said phase being essentially composed of solid matters. This binder phase consists of a homogenised mixture of anionic tensides and solubility enhancers in mutually adjusted proportions such that, at the working temperature for granulate formation, the binder mixing phase becomes liquid or plastic even without the addition of water. The bleach activator granulates may be obtained by premixing the finely divided bleach activators with the components of the binder and with other additives if required, homogenising the mixture of substances, preferably at moderately raised temperatures, to form a compressible mass and extruding it under high pressure into a strand, cutting the strand to the required grain form and rounding it if necessary.

Description

Die Erfindung betrifft neue schütt- und rieselfähige Granulate, die als Hauptbestandteil Bleichaktivatoren für die Textilwäsche eingebettet in eine Bindemittelphase enthalten, wobei die Bindemittelphase Tenside enthält, die bei Raumtemperatur und mäßig erhöhten Temperaturen fest sind. Die Erfindung betrifft weiterhin ein Verfahren zur Herstellung dieser neuen Bleichaktivatorgranulate.The invention relates to new pourable and free-flowing granules which contain bleach activators for textile washing embedded in a binder phase as the main component, the binder phase containing surfactants which are solid at room temperature and moderately elevated temperatures. The invention further relates to a method for producing these new bleach activator granules.

Anorganische Peroxyverbindungen, die sich in Wasser unter Freisetzung von Wasserstoffperoxid lösen, wie Natriumperborat und Natriumpercarbonat, werden seit langem als Oxidationsmittel zu Desinfektions- und Bleichzwecken verwendet. Die Oxidationswirkung dieser Substanzen hängt in verdünnten Lösungen stark von der Temperatur ab. So erzielt man mit Perborat in alkalischen Bleichflotten erst bei Temperaturen oberhalb 60°C eine ausreichend schnelle Bleiche verschmutzter Textilien. Bei niedrigeren Temperaturen kann die Oxidationswirkung der anorganischen Perverbindungen durch Zusatz von Aktivatoren verbessert werden, für die zahlreiche Vorschläge in der Literatur bekannt geworden sind. Der Zusatz dieser Aktivatoren kann die Bleichwirkung wäßriger Peroxidflotten so weit steigern, daß diese schon im Temperaturbereich von 30 bis 60 °C aktiv sind, d. h. bei Temperaturen, die für das Waschen empfindlicher Textilien gefordert werden.Inorganic peroxy compounds that dissolve in water releasing hydrogen peroxide, such as sodium perborate and sodium percarbonate, have long been used as oxidizing agents for disinfection and bleaching purposes. The oxidizing effect of these substances in dilute solutions depends strongly on the temperature. With perborate in alkaline bleaching liquors, sufficiently quick bleaching of soiled textiles can only be achieved at temperatures above 60 ° C. At lower temperatures, the oxidation effect of the inorganic per-compounds can be improved by adding activators, for which numerous proposals have become known in the literature. The addition of these activators can increase the bleaching effect of aqueous peroxide liquors to such an extent that they are already active in the temperature range from 30 to 60 ° C., ie. H. at temperatures required for washing delicate textiles.

Diese Aktivatoren, beispielsweise aus der Klasse der N- und O-Acylverbindungen sind allerdings stark hydrolyseempfindlich, vor allem in Gegenwart der in Waschmitteln allgemein üblichen Alkalien. Die sich daraus für die Lagerstabilität der Textilwaschmittel ableitenden Probleme werden dadurch verstärkt, daß die Aktivatoren häufig in Wasser schlecht löslich sind, so daß zum Einsatz feinstpulvrige Materialien mit schneller Dispergierbarkeit kommen sollen. Diese feinstteilige Form ermöglicht aber aufgrund der vergrößerten Oberfläche die verstärkte Hydrolyse der Aktivatoren bei ihrer Lagerung.However, these activators, for example from the class of the N- and O-acyl compounds, are highly sensitive to hydrolysis, especially in the presence of the alkalis which are generally customary in detergents. The problems derived from this for the storage stability of the textile detergents are exacerbated by the fact that the activators are often poorly soluble in water, so that finely powdered materials with rapid dispersibility should be used. This very finely divided form allows due to increased surface area the increased hydrolysis of the activators during their storage.

Zur Abhilfe sieht die Praxis vor, die Bleichaktivatorkomponente in Form getrennt hergestellter Granulate den trockenen Wasch- bzw. Reinigungsmittelgemischen zuzusetzen, wobei die Agglomerate feinster Bleichmittelteilchen mit Hilfsstoffen überzogen sind. Als Granulierhilfsstoffe und Überzugsmaterialien für solche Aktivatorgranulate sind die verschiedenartigsten organischen und anorganischen Substanzen vorgeschlagen worden. Bekannt ist insbesondere der Einsatz von bei Raumtemperatur festen tensidischen Verbindungen aus den Klassen der anionischen, kationischen und/oder nichtionischen Tenside, polymere Materialien oder Wachse. Bezüglich Einzelheiten zum Stand der Technik wird auf die ältere, nicht vorveröffentlichte deutsche Patentanmeldung P 40 24 759.7 hingewiesen, die ebenfalls Bleichaktivatoren in Granulatform betrifft.To remedy this, practice provides for the bleach activator component in the form of separately produced granules to be added to the dry washing or cleaning agent mixtures, the agglomerates of very fine bleaching agent particles being coated with auxiliaries. A wide variety of organic and inorganic substances have been proposed as granulation aids and coating materials for such activator granules. In particular, it is known to use surfactant compounds from the classes of anionic, cationic and / or nonionic surfactants, polymeric materials or waxes which are solid at room temperature. With regard to details of the prior art, reference is made to the older, unpublished German patent application P 40 24 759.7, which also relates to bleach activators in the form of granules.

Gegenstand der US-Patentschrift 4 486 327 und der älteren deutschen Anmeldung P 40 24 759.7 sind Granulate, in denen der feinteilige Bleichaktivator in eine als Bindemittel dienende praktisch wasserfreie Phase aus einem Gemisch anionischer und nichtionischer Tensidverbindungen eingebettet ist, wobei diese Granulate durch Extrusion des plastifizierten Gemisches bei erhöhter Temperatur hergestellt werden. Je nach Qualität des verwendeten nichtionischen Tensids haben sich diese Granulate entweder als zu langsam löslich bei niedrigen Temperaturen erwiesen oder aber sie besaßen eine so hohe Sprödigkeit, daß beim Abrunden der Granulatkörner ein unvertretbar hoher Anteil an feinkörnigem Material anfiel.The subject of US Pat. No. 4,486,327 and the earlier German application P 40 24 759.7 are granules in which the finely divided bleach activator is embedded in a practically anhydrous phase which serves as a binder and consists of a mixture of anionic and nonionic surfactant compounds, these granules being produced by extrusion of the plasticized one Mixture can be produced at elevated temperature. Depending on the quality of the nonionic surfactant used, these granules have either proven to be too slowly soluble at low temperatures or they were so brittle that an unacceptably high proportion of fine-grained material was obtained when the granules were rounded off.

Aufgabe der vorliegenden Erfindung war es daher, die oben genannten Nachteile der bisherigen Granulate zu vermeiden, ohne deren Vorteile, insbesondere die hohe Lagerstabilität und die leichte Herstellbarkeit, aufzugeben.The object of the present invention was therefore to avoid the above-mentioned disadvantages of the previous granules, without giving up their advantages, in particular the high storage stability and the ease of manufacture.

Die Lösung dieser Aufgabe gelang durch besondere Auswahl der als Bindemittel dienenden Komponenten so, daß das Herstellverfahren im übrigen beibehalten werden konnte.This problem was solved by special selection of the components serving as binders so that the manufacturing process could otherwise be retained.

Gegenstand der Erfindung ist ein schütt- und rieselfähiges Granulat, das als Hauptbestandteil Bleichaktivatoren für die Textilwäsche als feindisperse Feststofffphase eingebettet in eine das Granulatkorn durchdringende und als Bindemittel dienende praktisch wasserfreie Phase enthält und das durch Extrusion eines praktisch wasserfreien Gemisches aus Bleichaktivator, Aniontensid, Solubilisierungshilfsmittel und gegebenenfalls weiteren Zusatzstoffen hergestellt wird, dadurch gekennzeichnet, daß das Solubilisierungshilfsmittel ausgewählt ist aus der Gruppe Polyethylenglykol, Polypropylenglykol, an einer oder beiden Hydroxylgruppen anionisch modifiziertes Polyethylenglykol, an einer oder beiden Hydroxylgruppen anionisch modifiziertes Polypropylenglykol und Gemische dieser Verbindunqen.The invention relates to a pourable and free-flowing granulate which contains bleach activators for textile washing as a finely dispersed solid phase as the main constituent, embedded in a practically anhydrous phase penetrating the granulate grain and serving as a binder, and which is obtained by extrusion of a practically water-free mixture of bleach activator, anionic surfactant, solubilizing aid and optionally further additives are produced, characterized in that the solubilization aid is selected from the group consisting of polyethylene glycol, polypropylene glycol, anionically modified polyethylene glycol on one or both hydroxyl groups, anionically modified polypropylene glycol on one or both hydroxyl groups, and mixtures of these compounds.

Ein weiterer Gegenstand der Erfindung ist ein Verfahren zur Herstellung des Granulats, bei dem man den feinteiligen Bleichaktivator mit den übrigen Komponenten vormischt, das Stoffgemisch bei bevorzugt erhöhter Temperatur zu einer strangförmig verpreßbaren Masse homogenisiert und unter Anwendung erhöhten Drucks strangförmig extrudiert, die austretenden Stränge, gegebenenfalls nach Kühlung, in kurze Stücke schneidet und diese Stücke gegebenenfalls abrundet und, soweit gewünscht, nach Größe klassiert.Another object of the invention is a process for the production of the granules, in which the finely divided bleach activator is premixed with the other components, the mixture of substances is homogenized at a preferably elevated temperature to form an extrudable mass and extruded in the form of a strand using increased pressure, the emerging strands, if appropriate after cooling, cuts into short pieces and rounds off these pieces if necessary and, if desired, classified according to size.

Wesentlich an der Lehre der Erfindung ist der gemeinsame Einsatz von anionischen Tensiden und Solubilisierungshilfsmitteln in den Bleichaktivatorgranulaten. Beide Komponenten zusammen können Binderfunktionen und Hüllfunktionen übernehmen und dabei so ausgewählt werden, daß die Mischung aller Granulatbestandteile bei Raumtemperatur oder nur mäßig erhöhter Temperatur plastische Eigenschaften annehmen und strangförmig extrudierbar sind. Trotz dieser Eigenschaft sind die erhaltenen Granulate bei den Temperaturen, denen sie während der späteren Lagerung üblicherweise ausgesetzt sind, nicht klebrig und bleiben rieselfähig. Gleichzeitig wird durch die Verwendung der oben genannten Komponenten als Bindemittel eine hohe Lagerstabilität, insbesondere in feuchter Atmosphäre und in Gegenwart anderer Waschmittelbestandteile erreicht.What is essential to the teaching of the invention is the joint use of anionic surfactants and solubilization aids in the bleach activator granules. Both components together can take on binder functions and envelope functions and can be selected so that the mixture of all the granulate components takes on plastic properties at room temperature or only moderately elevated temperature and can be extruded in the form of a strand. Despite this property, the granules obtained are not tacky at the temperatures to which they are usually exposed during later storage and remain free-flowing. At the same time, the use of the above-mentioned components as binders achieves high storage stability, especially in a humid atmosphere and in the presence of other detergent components.

Vorzugsweise wird das als Bindemittel dienende Gemisch aus Aniontensid und Solubilisierungshilfsmittel so gewählt, daß dieses Gemisch erst bei Temperaturen oberhalb der höchsten üblichen Lagertemperaturen, d. h. oberhalb von Temperaturen von etwa 35 bis 40 °C erweicht. Die Granulierung erfolgt dann im darüberliegenden Temperaturbereich, wobei dann, wenn temperaturempfindliche Bleichaktivatoren oder Granulatkomponenten verwendet werden, entsprechende obere Grenztemperaturen eingehalten werden müssen. Vorzugsweise liegen die Arbeitstemperaturen bei der Granulierung nicht über 90 °C, insbesondere nicht über 80 °C, wobei Arbeitstemperaturen im Bereich von etwa 45 bis 75 °C besonders geeignet sein können.The mixture of anionic surfactant and solubilizing aid which serves as the binder is preferably selected so that this mixture only softens at temperatures above the highest usual storage temperatures, ie above temperatures of about 35 to 40 ° C. The granulation then takes place in the temperature range above, and if temperature-sensitive bleach activators or granulate components are used, corresponding upper limit temperatures must be observed. Preferably the working temperatures during the granulation are not above 90 ° C., in particular not above 80 ° C., whereby working temperatures in the range from about 45 to 75 ° C. may be particularly suitable.

Erfindungsgemäß kann es bevorzugt sein, die Aniontensidkomponente als den größeren Anteil im Bindemittelgemisch zu wählen. Insbesondere ist hier bevorzugt, entsprechende bei Raum- und Granulatbildungstemperatur feste aniontensidische Verbindungen einzusetzen, die wenigstens 55 Gew.-% und bis zu 98 Gew.-% des Bindemittelgemisches ausmachen können. In zweckmäßiger Ausgestaltung liegt der Aniontensidanteil im Bereich von 60 bis 95 Gew.-%, insbesondere 60 bis 85 Gew.-%, bezogen auf Gewicht des Bindemittelgemisches. Bezogen auf das Gesamtgewicht des Granulats liegt der Anteil vorzugsweise bei 4 bis 25 Gew.-%, insbesondere bei 6 bis 15 Gew.-%.According to the invention, it may be preferred to choose the anionic surfactant component as the larger proportion in the binder mixture. It is particularly preferred here to use corresponding anionic surfactant compounds which are solid at room temperature and granulate formation temperature and which can make up at least 55% by weight and up to 98% by weight of the binder mixture. In an expedient embodiment, the anionic surfactant content is in the range from 60 to 95% by weight, in particular 60 to 85% by weight, based on the weight of the binder mixture. Based on the total weight of the granulate, the proportion is preferably 4 to 25% by weight, in particular 6 to 15% by weight.

Geeignete feste Aniontenside sind die in der Waschmitteltechnologie insbesondere im Rahmen von Textilwaschmitteln bekannten festen Komponenten, die insbesondere zu den nachfolgenden Stoffklassen zählen: Alkylsulfate, Alkylsulfonate, Alkylarylsulfonate, sulfonierte Fettsäureester und/oder Seifen. Besonders geeignete Aniontenside sind beispielsweise C12-C18-Fettalkoholsulfate, die einzeln oder im Gemisch vorliegen können wie Laurylsulfat, Myristylsulfat und hier insbesondere C16-C18-Talgalkoholsulfat. Andere geeignete spezielle Aniontensidkomponenten sind Alkylbenzolsulfonate (ABS) mit 9 bis 13 C-Atomen in der Alkylkette, insbesondere C12-Alkylbenzolsulfonat, waschaktive Salze von alpha-sulfonierten Fettsäuremethylestern und/oder Natriumseifen von Fettsäuren, insbesondere der Fettsäuren mit 12 bis 18 C-Atomen. Ebenfalls können sich die Salze langkettiger Estercarbonsäuren eignen, wie sie aus Fettalkoholen mit 8 bis 18 C-Atomen und Di- oder Polycarbonsäuren, beispielsweise Maleinsäureanhydrid oder Zitronensäure, erhältlich sind. Vorzugsweise werden die anionischen Tenside in Form der Natriumsalze eingesetzt. Durch Mitverwendung ungesättigter Komponenten und/oder durch Einsatz von Kaliumseifen kann auf die Plastifizierbarkeit des Bindemittelgemisches bei den erhöhten Arbeitstemperaturen Einfluß genommen werden.Suitable solid anionic surfactants are the solid components known in detergent technology, in particular in the context of textile detergents, which belong in particular to the following classes of substances: alkyl sulfates, alkyl sulfonates, alkylarylsulfonates, sulfonated fatty acid esters and / or soaps. Particularly suitable anionic surfactants are, for example, C 12 -C 18 fatty alcohol sulfates, which can be present individually or in a mixture, such as lauryl sulfate, myristyl sulfate and here in particular C 16 -C 18 tallow alcohol sulfate. Other suitable special anionic surfactant components are alkylbenzenesulfonates (ABS) with 9 to 13 carbon atoms in the alkyl chain, in particular C 12 alkylbenzenesulfonate, wash-active salts of alpha-sulfonated fatty acid methyl esters and / or sodium soaps of fatty acids, in particular of fatty acids with 12 to 18 carbon atoms . The salts of long-chain ester carboxylic acids, such as those obtainable from fatty alcohols having 8 to 18 carbon atoms and di- or polycarboxylic acids, for example maleic anhydride or citric acid, may also be suitable. The anionic surfactants are preferably used in the form of the sodium salts. The use of unsaturated components and / or the use of potassium soaps can influence the plasticizability of the binder mixture at the elevated working temperatures.

Bei den erfindungsgemäß als Solubilisierungshilfsmittel eingesetzten Verbindungen handelt es sich um Polyethylen- und/oder Polypropylenglykole oder Derivate dieser Verbindungen. Das mittlere Molekulargewicht dieser Polymeren liegt vorzugsweise im Bereich zwischen etwa 200 und etwa 12 000. Besonders bevorzugt werden Polyethylenglykole mit einem mittleren Molekulargewicht zwischen 600 und 4000. Bei den erfindungsgemäß geeigneten Derivaten der Polyalkylenglykole handelt es sich um Polymere, die an einer oder beiden endständigen Hydroxylgruppen anionisch modifiziert sind. Geeignet sind die Sulfate und/oder insbesondere die Disulfate der oben genannten Polyalkylenglykole. Ebenso geeignet sind die Sulfosuccinate und/oder Disulfosuccinate dieser Polyalkylenglykole. Vorzugsweise leiten sich diese anionischen Derivate von Polyglykolen mit mittleren Molekulargewichten zwischen 600 und 6000, insbesondere von solchen mit mittleren Molekulargewichten zwischen 1000 und 4000 ab. Die anionischen Derivate können als Salze beliebiger Kationen vorliegen, werden jedoch vorzugsweise als Alkalisalze, insbesondere als Natrium- oder Kaliumsalze, sowie als Salze organischer Amine, beispielsweise von Triethanolamin eingesetzt.The compounds used as solubilization aids according to the invention are polyethylene and / or polypropylene glycols or derivatives of these compounds. The average molecular weight of these polymers is preferably in the range between about 200 and about 12,000. Polyethylene glycols with an average molecular weight between 600 and 4,000 are particularly preferred. The derivatives of the polyalkylene glycols which are suitable according to the invention are polymers which have one or both terminal hydroxyl groups are anionically modified. The sulfates and / or in particular the disulfates of the abovementioned polyalkylene glycols are suitable. The sulfosuccinates and / or disulfosuccinates of these polyalkylene glycols are also suitable. These anionic derivatives are preferably derived from polyglycols with average molecular weights between 600 and 6000, in particular from those with average molecular weights between 1000 and 4000. The anionic derivatives can be present as salts of any cations, but are preferably used as alkali salts, in particular as sodium or potassium salts, and as salts of organic amines, for example triethanolamine.

Vorzugsweise werden auch Mischungen der Polyalkylenglykolether und ihrer anionisch modifizierten Derivate in einem beliebigen Mischungsverhältnis eingesetzt. Insbesondere ist dabei eine Mischung aus Polyalkylenglykol und den Sulfosuccinaten und/oder Disulfosuccinaten der Polyalkylenglykole bevorzugt. Geeignet ist aber auch eine Mischung aus Polyalkylenglykol und den entsprechenden Sulfaten und/oder Disulfaten und eine Mischung aus Polyalkylenglykol, den entsprechenden Sulfaten und/oder Disulfaten und den entsprechenden Sulfosuccinaten und/oder Disulfosuccinaten. Der Anteil des Solubilisierungshilfsmittels am Granulat beträgt vorzugsweise 0,5 bis 15 Gew.-%, insbesondere 1 bis 6 Gew.-%.Mixtures of the polyalkylene glycol ethers and their anionically modified derivatives are preferably also used in any mixing ratio. In particular, a mixture of polyalkylene glycol and the sulfosuccinates and / or disulfosuccinates of the polyalkylene glycols is preferred. However, a mixture of polyalkylene glycol and the corresponding sulfates and / or disulfates and a mixture of polyalkylene glycol, the corresponding sulfates and / or disulfates and the corresponding sulfosuccinates and / or disulfosuccinates are also suitable. The proportion of the solubilization aid in the granulate is preferably 0.5 to 15% by weight, in particular 1 to 6% by weight.

In der erfindungsgemäß wichtigsten Ausführungsform werden als Bindemittel solche Gemische aus Aniontensid und Solubilisierhilfsmittel eingesetzt, die bei Arbeitstemperatur der Granulierung hochwirksame Plastifiziermittel sind, so daß schon mit beschränkten Mengen des Bindemittels die gewünschte plastifizierte Gutbeschaffenheit eingestellt werden kann. Die Bindemittelmengen liegen in dieser Ausführungsform vorzugsweise unterhalb etwa 50 Gew.-% des Gesamtgemisches, vorzugsweise liegt in diesem Gesamtgemisch der Bleichaktivator in Mengen von etwa 70 bis 95 Gew.-% vor. Besonders geeignete Aktivatorgehalte können im Bereich von etwa 75 bis 90 Gew.-%, bezogen auf das gesamte Granulat, liegen. Der Rest des Granulatkorns wird durch das Bindemittel oder wenigstens zu einem substantiellen Anteil durch dieses tensidische Bindemittel gebildet. In wichtigen Ausführungsformen enthalten die Granulate das Bindemittelgemisch wenigstens zu etwa 3 Gew.-%, vorzugsweise zu wenigstens etwa 5 Gew.-%, bezogen jeweils auf das gesamte Granulat, wobei Bindemittelmengen im Bereich von etwa 7 bis 25 Gew.-% besonders bevorzugt sein können.In the most important embodiment according to the invention, mixtures of anionic surfactant and solubilizing aids are used as binders which are highly effective plasticizers at the working temperature of the granulation, so that the desired plasticized good quality can be set with limited amounts of the binder. In this embodiment, the amounts of binder are preferably below about 50% by weight of the total mixture, and the bleach activator is preferably present in this total mixture in amounts of about 70 to 95% by weight. Particularly suitable activator contents can range from about 75 to 90% by weight on the entire granulate. The rest of the granulate is formed by the binder or at least to a substantial extent by this surfactant binder. In important embodiments, the granules contain at least about 3% by weight, preferably at least about 5% by weight, of the binder mixture, based in each case on the entire granulate, binder amounts in the range from about 7 to 25% by weight being particularly preferred can.

Die im Verfahren unmittelbar anfallenden rieselfähigen praktisch wasserfreien Kompaktate können als Bleichaktivatoren alle heute für diesen Einsatzzweck bekannten Stoffe bzw. Stoffgemische enthalten. Der Vollständigkeit halber seien die Stoffe noch einmal wie folgt zusammengefaßt: Geeignete Bleichaktivatoren für Perverbindungen sind dementsprechend 0- und/ oder N-acylierte Verbindungen wie Pentaacetylglucose (PAG), Pentapropionylglucose (PPG), Tetraacetylethylendiamin (TAED), Tetraacetylglycoluril (TAGU), Triacetylethanolamin (TAEA), acylierte Triazinderivate wie 1,5-Diacetyl-2,4-dioxohexahydro-1,3,5-triazin (DADHT), Carbonsäureanhydride, wie Bernsteinsäure-, Benzoesäure- oder Phthalsäureanhydrid, Salze gemischter Anhydride, wie Natrium- oder Magnesiumdiacetylphosphat (NADAP bzw. MGDAP), Phenolester wie p-Carboxylphenylacetat, p-Sulfonylphenylacetat, sowie weitere Phenolester mit einem anionischen Substituenten am Phenylrest. Das erfindungsgemäße Verfahren zur Herstellung der Bleichaktivatorgranulate ist in einer besonderen Ausführungsform dadurch gekennzeichnet, daß man das Mehrstoffgemisch zunächst im Bereich der Raumtemperatur oder nur mäßig erhöhter Temperaturen in einer geeigneten Mischungsvorrichtung möglichst gleichmäßig vermischt. Als Mischvorrichtung sind alle üblichen entsprechenden Geräte, beispielsweise von der Art des Lödige-Pflugschar-Mischers geeignet. Dieses Vorgemisch wird dann der Stufe der Homogenisierung und strangförmigen Verpressung zugeführt. Wenn auch grundsätzlich beliebige Homogenisier- und Extrusionsvorrichtungen - beispielsweise linear arbeitende Schneckenextruder - geeignet sind, so hat sich doch für die Durchführung des erfindungsgemäßen Verfahrens eine Verarbeitungsvorrichtung als besonders geeignet erwiesen. Hierbei handelt es sich um die strangförmige Verpressung mittels einer Pelletpresse. Dabei kann das Arbeiten in Vorrichtungen dieses Typs mit temperierbarem Koller (Preßrolle) zweckmäßig sein, wie sie im einzelnen in der DE 38 16 842 beschrieben sind. Mittels dieses temperierbaren Kollers kann die Guttemperatur im Arbeitsraum der Pelletpresse auf vorbestimmte Werte eingestellt werden, wobei hier der zuvor genannte Temperaturbereich bis maximal 90 °C und vorzugsweise von 45 bis 70 °C gewählt wird.The free-flowing, practically water-free compactates that directly occur in the process can contain as bleach activators all substances or substance mixtures known today for this purpose. For the sake of completeness, the substances are summarized again as follows: Accordingly, suitable bleach activators for per-compounds are 0- and / or N-acylated compounds such as pentaacetylglucose (PAG), pentapropionylglucose (PPG), tetraacetylethylenediamine (TAED), tetraacetylglycoluril (TAGUanol, triacetylamine) TAEA), acylated triazine derivatives such as 1,5-diacetyl-2,4-dioxohexahydro-1,3,5-triazine (DADHT), carboxylic anhydrides such as succinic, benzoic or phthalic anhydride, salts of mixed anhydrides such as sodium or magnesium diacetyl phosphate ( NADAP or MGDAP), phenol esters such as p-carboxylphenylacetate, p-sulfonylphenylacetate, and further phenol esters with an anionic substituent on the phenyl radical. In a particular embodiment, the process according to the invention for producing the bleach activator granules is characterized in that the multicomponent mixture is first mixed as uniformly as possible in a suitable mixing device in the region of room temperature or only moderately elevated temperatures. All customary devices, for example of the Lödige ploughshare mixer type, are suitable as the mixing device. This premix is then fed to the homogenization and extrusion stage. Although basically any homogenizing and extrusion devices - for example linear screw extruders - are suitable, a processing device has proven to be particularly suitable for carrying out the method according to the invention. This is the extrusion by means of a pellet press. It can be useful to work in devices of this type with a temperable roller (press roller), as described in detail in DE 38 16 842 are. The temperature of the material in the working space of the pellet press can be set to predetermined values by means of this temperable pan, the aforementioned temperature range up to a maximum of 90 ° C. and preferably from 45 to 70 ° C. being selected here.

Das abgelängte Granulat wird erforderlichenfalls einer Schockkühlung unterworfen. Als Kühlmedium kann hier Luft oder gekühlte Luft eingesetzt werden. Zusätzlich oder alternativ kann das primär extrudierte und abgelängte Granulat mit feinstteiligen Feststoffen oberflächlich beladen werden. Beispiele hierfür sind pulverförmige Zeolithe, insbesondere Zeolith NaA von Waschmittelqualität, Talkum, Kieselsäure und dergleichen.If necessary, the cut granulate is subjected to shock cooling. Air or cooled air can be used as the cooling medium. Additionally or alternatively, the primarily extruded and cut granulate can be superficially loaded with particulate solids. Examples include powdered zeolites, especially detergent grade zeolite NaA, talc, silica and the like.

Es kann erwünscht oder zweckmäßig sein, in das Granulatkorn neben den feinstteiligen festen Bleichaktivatoren und dem Bindemittel weitere Hilfs- oder Zusatzstoffe einzuarbeiten. Der Anteil dieser Zusatzstoffe beträgt vorzugweise nicht über 10 Gew.-%, bezogen auf das Granulat.It may be desirable or expedient to incorporate further auxiliaries or additives into the granulate in addition to the finely divided solid bleach activators and the binder. The proportion of these additives is preferably not more than 10% by weight, based on the granules.

Besonders zu erwähnen sind in diesem Zusammenhang feinstverteilte leicht lösliche Alkalisalze anorganischer oder organischer Säuren. Der Zusatz dieser Stoffe kann in Einzelfällen eine weitere Beschleunigung der Aktivatorfreisetzung beim Eintrag des Granulats in Wasser bewirken. Besonders geeignete Salze sind Natriumcarbonat, Natriumsulfat und Natriumcitrat. Der Anteil dieser Salze an den Granulaten liegt vorzugsweise nicht über 10 Gew.-%, bezogen auf des Gesamtgewicht des Granulats, insbesondere liegt er zwischen etwa 0,5 Gew.-% und etwa 5 Gew.-%.Particularly noteworthy in this context are finely divided, readily soluble alkali salts of inorganic or organic acids. The addition of these substances can in individual cases further accelerate the release of the activator when the granules are introduced into water. Particularly suitable salts are sodium carbonate, sodium sulfate and sodium citrate. The proportion of these salts in the granules is preferably not more than 10% by weight, based on the total weight of the granules, in particular it is between about 0.5% by weight and about 5% by weight.

Als weitere Zusatzstoffe kommen beispielsweise Farbstoffe in Betracht, wie sie im Waschmittelsektor üblich sind. Zur Einarbeitung dieser Stoffe kann es zweckmäßig sein, sie in flüssigen Granulatbestandteile vor deren Einmischung zu suspendieren oder zu lösen. Bevorzugte Farbstoffe sind Pigmentfarbstoffe, wie Kupferphthalocyanin-Farbstoffe. Zur besseren Verteilung des Farbstoffs in den Granulaten kann es vorteilhaft sein, den Farbstoff vor der Zugabe in geringen Mengen an Wasser zu dispergieren. Die Wassermenge soll dabei nicht über 1 Gew.-%, vorzugsweise nicht mehr als 0,5 Gew.-%, bezogen auf das Gesamtgewicht des Granulats betragen. Beispiele weiterer geeigneter Hilfsstoffe sind Sprengmittel und Gleitmittel.Other additives which may be used are, for example, dyes as are customary in the detergent sector. To incorporate these substances, it may be appropriate to suspend or dissolve them in liquid granulate components before they are mixed in. Preferred dyes are pigment dyes, such as copper phthalocyanine dyes. For better distribution of the dye in the granules, it may be advantageous to disperse the dye in small amounts of water before the addition. The amount of water should not be more than 1% by weight, preferably not more than 0.5% by weight, based on the total weight of the granules. Examples of other suitable auxiliaries are disintegrants and lubricants.

Bei der Extrusion des auf Arbeitstemperatur gebrachten Mehrstoffgemisches können Verdichtungsverhältnisse dergestalt eingestellt werden, daß die fertigen Granulate Schüttgewichte von wenigstens 500 g/l aufweisen. Geeignet sind hier insbesondere Schüttgewichte im Bereich bis 1000 g/l, wobei Schüttgewichte im Bereich von 600 bis 900 g/l bevorzugt sein können. Dabei kann durch Wahl der jeweils vorgegebenen Extrusionsdrucke und sonstigen Verarbeitungsbedingungen in Abhängigkeit von den Stoffeigenschaften des Mehrkomponentengemisches praktisch jeder im Einzelfall gewünschte Dichtebereich im Granulatkorn zielgerichtet eingestellt werden.During the extrusion of the multicomponent mixture brought to working temperature, compression ratios can be set such that the finished granules have bulk densities of at least 500 g / l. Bulk weights in the range up to 1000 g / l are particularly suitable, bulk densities in the range 600 to 900 g / l being preferred. By choosing the respectively specified extrusion pressures and other processing conditions, depending on the material properties of the multi-component mixture, practically every density range desired in the individual granules can be set in a targeted manner.

Bevorzugte Granulatkörner besitzen entweder Zylinder- oder Kugelform. Die zusätzliche Abrundung der zylindrischen Formen kann zweckmäßigerweise unmittelbar im Anschluß an das Ablängen am noch hinreichend warmen Granulatkorn erfolgen. Zur Abrundung geeignete Hilfsvorrichtungen sind bekannt, zu nennen sind hier beispielsweise die zu diesem Zweck eingesetzten Marumerizer.Preferred granules are either cylindrical or spherical. The additional rounding of the cylindrical shapes can expediently take place immediately after cutting to length on the still sufficiently warm granulate. Auxiliary devices suitable for rounding off are known, for example the Marumerizers used for this purpose.

Die Korngröße der Granulate wird in an sich bekannter Weise geregelt und zweckmäßigerweise auf den Bereich von 0,7 bis 3 mm eingestellt. So kann die Ablängung der Granulate beispielsweise auf die gewünschte Kornlänge von 0,7 bis 3 mm oder darüber hinaus, beispielsweise auf eine Kornlänge von 5 mm erfolgen. Diese zylinderförmigen Granulate mit Längen oberhalb 3 mm werden anschließend auf eine vorbestimmte Länge gebrochen und gegebenenfalls verrundet, so daß eine Länge von 3 mm nicht überschritten wird. Zylinderförmige Granulate besitzen vorzugsweise eine Länge bis zu 2 mm, während zusätzlich abgerundete, vorzugsweise kugelförmige Granulate einen Teilchdurchmesser im Bereich von 0,4 mm bis 1,6 mm aufweisen.The grain size of the granules is regulated in a manner known per se and is expediently set in the range from 0.7 to 3 mm. For example, the granules can be cut to the desired grain length of 0.7 to 3 mm or beyond, for example to a grain length of 5 mm. These cylindrical granules with lengths above 3 mm are then broken to a predetermined length and rounded if necessary so that a length of 3 mm is not exceeded. Cylindrical granules preferably have a length of up to 2 mm, while additionally rounded, preferably spherical granules have a particle diameter in the range from 0.4 mm to 1.6 mm.

BeispieleExamples

Zur Herstellung der granularen Bleichaktivatoren wurden die jeweiligen Bestandteile in den in der Tabelle dargestellten Mischungsverhältnissen in einem Pflugscharmischer (Fa. Lödige, Deutschland) eine Minute intensiv vermischt. Das so erhaltene Vorgemisch wurde anschließend kontinuierlich einer Ringmatrizenpresse (Pelletpresse, Ausführungsform gemäß DE 38 16 842, Fa. Schlüter, Deutschland), deren temperierbarer Koller (Preßrolle) auf 50°C aufgeheizt war, zugeführt. Während der Durchführung des Verfahrens kam es zu leichten Temperaturschwankungen, wobei die Temperatur der Preßrolle nicht unter 45°C absank und nicht über 60°C anstieg. Der Durchmesser der Preßkanäle, mit denen die Ringmatrize durchsetzt war, betrug 1,2mm. Der Abstand zwischen Preßrolle und Ringmatrize betrug 1,5 mm. Durch ein an der Außenseite der Ringmatrize angebrachtes Messer wurde der austretende Strang jeweils in einer Länge von 1,5 mm abgeschnitten. Die Schüttgewichte der Granulate lagen zwischen 630 und 700 g/l. Anschließend wurden die abgelängten Granulate in einem marktgängigen Rondiergerät vom Typ Marumerizer verrundet. Dabei ging der Gutkornanteil (Siebfraktion zwischen 0,4 und 1,6 mm) der Granulate nur wenig zurück.To produce the granular bleach activators, the respective constituents were mixed intensively for one minute in a ploughshare mixer (Lödige, Germany) in the mixing ratios shown in the table. The premix obtained in this way was then fed continuously to a ring die press (pellet press, embodiment according to DE 38 16 842, Schlüter, Germany), the temperature-controlled roller (press roll) of which was heated to 50.degree. During the implementation of the process, there were slight temperature fluctuations, the temperature of the press roll not dropping below 45 ° C. and not rising above 60 ° C. The diameter of the press channels with which the ring die was penetrated was 1.2 mm. The distance between the press roller and the ring die was 1.5 mm. The emerging strand was cut to a length of 1.5 mm by a knife attached to the outside of the ring die. The bulk weights of the granules were between 630 and 700 g / l. The cut-to-length granules were then rounded off in a Marumerizer-type rounding machine. The proportion of good grain (sieve fraction between 0.4 and 1.6 mm) of the granules decreased only slightly.

Zur Bestimmung der Lösegeschwindigkeit der Granulate wurde je 0,5 g der abgerundeten und gesiebten Granulate in 1 Liter Wasser (17° deutsche Härte) von 40 °C in einem Becherglas 5 Minuten lang mit einem Flügelrührer bei 700 Umdrehungen pro Minute gerührt. Nach dieser Zeit wurde der gesamte Inhalt durch ein Metallsieb der Maschenweite 0,1 mm filtriert und das Sieb mit dem Rückstand bis zur Gewichtskonstanz bei Raumtemperatur getrocknet. Die Menge des Rückstands wird in der Tabelle in % bezogen auf die Einwaage an Granulat angegeben. Die Löslichkeit wurde zum einen an frisch hergestelltem Granulat, zum anderen an solchem Granulat bestimmt, das 5 Tage bei 40 °C gelagert worden war.To determine the dissolving speed of the granules, 0.5 g of the rounded and sieved granules were stirred in 1 liter of water (17 ° German hardness) at 40 ° C. in a beaker for 5 minutes with a paddle stirrer at 700 revolutions per minute. After this time, the entire contents were filtered through a metal sieve with a mesh size of 0.1 mm and the sieve with the residue was dried to constant weight at room temperature. The amount of the residue is given in the table in% based on the weight of granules. The solubility was determined on the one hand on freshly prepared granules and on the other hand on such granules which had been stored at 40 ° C. for 5 days.

Aus den in der Tabelle angegebenen Werten sind die vorteilhaften Eigenschaften der erfindungsgemäßen Granulate 1 bis 6 gegenüber den analog zur älteren Anmeldung DE P 40 24 759.7 hergestellten Granulate 7 bis 12 klar erkennbar. (EO in der Tabelle bedeutet Ethylenoxid.)

Figure imgb0001
From the values given in the table, the advantageous properties of the granules 1 to 6 according to the invention compared to the granules 7 to 12 produced analogously to the earlier application DE P 40 24 759.7 can be clearly seen. (EO in the table means ethylene oxide.)
Figure imgb0001

Claims (10)

  1. Pourable and free-flowing granules which contain as their principal component bleach activators for the washing of laundry embedded as a finely dispersed solid phase in a substantially water-free phase permeating the granules and serving as binder and which are produced by extrusion of a substantially water-free mixture of bleach activator, anionic surfactant, solubilizing aid and optionally other additives, characterized in that the solubilizing aid is selected from the group consisting of polyethylene glycol, polypropylene glycol, polyethylene glycol anionically modified at one or both hydroxyl groups, polypropylene glycol anionically modified at one or both hydroxyl groups and mixtures of these compounds.
  2. Granules as claimed in claim 1 containing water-soluble alkali metal salt as a further additive.
  3. Granules as claimed in claim 1 or 2 containing
    70 to 95% by weight of bleach activator
    4 to 25% by weight of anionic surfactant
    0.5 to 15% by weight of solubilizing aid
    0 to 10% by weight of alkali metal salt.
  4. Granules as claimed in claim 3 containing
    75 to 90% by weight of bleach activator
    6 to 15% by weight of anionic surfactant
    1 to 6% by weight of solubilizing aid
    0.5 to 5% by weight of alkali metal salt.
  5. Granules as claimed in claim 1 or 2 in which the bleach activator is selected from the group consisting of pentaacetyl glucose, tetraacetyl ethylenediamine, 1,5-diacetyl-2,4-dioxohexahydro-1,3,5-triazine and mixtures thereof.
  6. Granules as claimed in claim 1 or 2, in which the anionic surfactant is selected from the group consisting of C12-18 fatty alcohol sulfates, alkylbenzenesulfonates containing 9 to 13 carbon atoms in the alkyl chain, α-sulfofatty acid methyl esters containing 12 to 18 carbon atoms in the carboxylic acid component and mixtures thereof.
  7. Granules as claimed in claim 1 or 2, in which the solubilizing aid is selected from the group consisting of polyethylene glycol, polypropylene glycol, sulfates and/or disulfates of polyethylene glycol or polypropylene glycol, sulfosuccinates and/or disulfosuccinates of polyethylene glycol or polypropylene glycol and mixtures thereof.
  8. Granules as claimed in claim 2, in which the alkali metal salt is selected from the group consisting of sodium carbonate, sodium sulfate, sodium citrate and mixtures thereof.
  9. A process for the production of the bleach activator granules claimed in claim 1, in which the fine-particle bleach activator is mixed with the other components, the resulting mixture is homogenized, preferably at elevated temperature, to form a paste extrudable in strand form and the paste obtained is extruded in strand form under elevated pressure, the issuing strands are cut into short pieces, optionally after cooling, and the pieces obtained are optionally spheronized and, if desired, graded according to size.
  10. A process as claimed in claim 9, in which the working temperature is allowed to rise to a value of at most 80°C and preferably to a value of about 45 to 75°C.
EP93901014A 1991-12-24 1992-12-15 Bleach activators in granular form (ii) Expired - Lifetime EP0618960B1 (en)

Applications Claiming Priority (3)

Application Number Priority Date Filing Date Title
DE4143016A DE4143016A1 (en) 1991-12-24 1991-12-24 BLEACH ACTIVATORS IN GRANULATE FORM (II)
DE4143016 1991-12-24
PCT/EP1992/002909 WO1993013194A1 (en) 1991-12-24 1992-12-15 Bleach activators in granular form (ii)

Publications (2)

Publication Number Publication Date
EP0618960A1 EP0618960A1 (en) 1994-10-12
EP0618960B1 true EP0618960B1 (en) 1996-07-10

Family

ID=6448159

Family Applications (1)

Application Number Title Priority Date Filing Date
EP93901014A Expired - Lifetime EP0618960B1 (en) 1991-12-24 1992-12-15 Bleach activators in granular form (ii)

Country Status (6)

Country Link
EP (1) EP0618960B1 (en)
JP (1) JPH07502551A (en)
KR (1) KR940703910A (en)
DE (2) DE4143016A1 (en)
ES (1) ES2089781T3 (en)
WO (1) WO1993013194A1 (en)

Cited By (1)

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Publication number Priority date Publication date Assignee Title
US11659838B2 (en) 2021-04-01 2023-05-30 Sterilex, Llc Quat-free powdered disinfectant/sanitizer

Families Citing this family (11)

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Publication number Priority date Publication date Assignee Title
US5534196A (en) * 1993-12-23 1996-07-09 The Procter & Gamble Co. Process for making lactam bleach activator containing particles
DE19515233A1 (en) * 1995-04-28 1996-10-31 Henkel Kgaa Storage-stable granules containing bleach activators and their production
DE19537980A1 (en) * 1995-10-12 1997-04-17 Henkel Kgaa Bleach activators in granular form (III)
HUP9901904A3 (en) * 1996-01-29 1999-11-29 Procter & Gamble Process for making particulate bleach activator component
CA2324397A1 (en) * 1998-03-19 1999-09-23 Donald Ray Brown Detergent composition containing cylindrically-shaped bleach activator extrudates having enhanced flowability
DE19959002C2 (en) * 1999-12-08 2002-12-05 Henkel Kgaa Process for the production of compacted particles
AR027014A1 (en) 1999-12-20 2003-03-12 Procter & Gamble PARTICULATE OF WHITENING ACITVATOR, DETERGENT COMPOSITION THAT INCLUDES IT AND AVERAGE HYDROLIGANCE METHOD OF A SALT MOLECULA
DE10134364A1 (en) * 2001-07-14 2003-01-23 Clariant Gmbh Process for the production of bleach activator granules
DE10136805A1 (en) 2001-07-25 2003-02-13 Clariant Gmbh Process for the production of bleach activator granules
DE10242222A1 (en) * 2002-09-12 2004-03-25 Henkel Kgaa Mechanically compacted washing or detergent agents containing neutralizable organic polycarboxylic acids are given improved odor values by having specific non-water-soluble builder content and pH
DE102006041292A1 (en) * 2006-09-01 2008-03-06 Henkel Kgaa Use of optionally substituted hexagonal heterocycle with a nitrogen in the ring for activating and improving the brightening effect of the hydrogen peroxide for keratin fibers such as fur, wool, feathers and human hair

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DE2224509A1 (en) * 1972-05-19 1973-12-13 Henkel & Cie Gmbh Bleaching aid - for washing and bleaching agents
DE3364205D1 (en) * 1982-10-08 1986-07-24 Procter & Gamble Bodies containing bleach activators
US4486327A (en) * 1983-12-22 1984-12-04 The Procter & Gamble Company Bodies containing stabilized bleach activators
US4678594A (en) * 1985-07-19 1987-07-07 Colgate-Palmolive Company Method of encapsulating a bleach and activator therefor in a binder
ATE107352T1 (en) * 1989-08-09 1994-07-15 Henkel Kgaa PRODUCTION OF COMPACT GRANULES FOR DETERGENT.
DE4014978A1 (en) * 1990-05-10 1991-11-14 Basf Ag METHOD FOR PRODUCING A GRAINY BLEACH ACTIVATOR COMPOSITION
DE4024759A1 (en) * 1990-08-03 1992-02-06 Henkel Kgaa BLEACH ACTIVATORS IN GRANULATE FORM

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US11659838B2 (en) 2021-04-01 2023-05-30 Sterilex, Llc Quat-free powdered disinfectant/sanitizer

Also Published As

Publication number Publication date
WO1993013194A1 (en) 1993-07-08
EP0618960A1 (en) 1994-10-12
ES2089781T3 (en) 1996-10-01
JPH07502551A (en) 1995-03-16
KR940703910A (en) 1994-12-12
DE59206759D1 (en) 1996-08-14
DE4143016A1 (en) 1993-07-01

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