EP0332050A1 - Activators for inorganic per compounds - Google Patents
Activators for inorganic per compounds Download PDFInfo
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- EP0332050A1 EP0332050A1 EP89103637A EP89103637A EP0332050A1 EP 0332050 A1 EP0332050 A1 EP 0332050A1 EP 89103637 A EP89103637 A EP 89103637A EP 89103637 A EP89103637 A EP 89103637A EP 0332050 A1 EP0332050 A1 EP 0332050A1
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- C—CHEMISTRY; METALLURGY
- C11—ANIMAL OR VEGETABLE OILS, FATS, FATTY SUBSTANCES OR WAXES; FATTY ACIDS THEREFROM; DETERGENTS; CANDLES
- C11D—DETERGENT COMPOSITIONS; USE OF SINGLE SUBSTANCES AS DETERGENTS; SOAP OR SOAP-MAKING; RESIN SOAPS; RECOVERY OF GLYCEROL
- C11D3/00—Other compounding ingredients of detergent compositions covered in group C11D1/00
- C11D3/39—Organic or inorganic per-compounds
- C11D3/3902—Organic or inorganic per-compounds combined with specific additives
- C11D3/3905—Bleach activators or bleach catalysts
- C11D3/3907—Organic compounds
- C11D3/3917—Nitrogen-containing compounds
- C11D3/392—Heterocyclic compounds, e.g. cyclic imides or lactames
Definitions
- Inorganic per-compounds especially hydrogen peroxide and solid per-compounds, which dissolve in water to release hydrogen peroxide, such as sodium perborate and sodium carbonate perhydrate, 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; For example, with H2O2 or perborate in alkaline bleaching liquors, sufficiently quick bleaching of soiled textiles can only be achieved at temperatures above about 80 ° C. At lower temperatures, the oxidation effect of the inorganic per compounds can be improved by adding so-called activators, for which numerous proposals have become known in the literature.
- carboxylic anhydrides have been proposed for this purpose (DE 893 049) and used in bleaching agents (DE 19 12 579). By adding these substances, the bleaching effect of aqueous peroxide liquors can be increased to such an extent that already at 60 ° C almost the same effects occur as with the peroxide liquor alone at 95 ° C.
- the present invention also aims to improve the oxidation and bleaching effect of inorganic per-compound at low temperatures below 80 ° C., in particular in the temperature range from approximately 15 to 45 ° C.
- isatoic anhydride and its derivatives can be used as activators wherever a particular increase in the oxidation activity of inorganic per-compounds is important at low temperatures, for. B. in the bleaching of textiles, hair or hard surfaces, in the oxidation of organic or inorganic intermediates and in disinfection. Most of these activators far outperform the best carbonic anhydride activators known to date.
- the use according to the invention is to create conditions under which hydrogen peroxide and isatoic anhydride or its derivatives can react with one another with the aim of obtaining secondary products which have a stronger oxidizing action.
- Such conditions exist in particular when the two reactants meet in an aqueous alkaline solution.
- the conditions can be varied widely depending on the intended use.
- mixtures of water and suitable organic solvents e.g. B. for the use in disinfection or in the oxidation of intermediates as a reaction medium in question.
- the pH of the reaction medium can be selected within wide limits, from the weakly acidic range (pH 4) to the strongly alkaline range (pH 13), depending on the application.
- the alkaline range from pH 8 to pH 11 is preferred since it is particularly advantageous for the activation reaction and the stability of the per compound formed.
- the activator according to the invention is also preferably used together with a sodium perborate or with sodium carbonate perhydrate, which already have pH values of this range in their solutions.
- Examples of other suitable per compounds are phosphate perhydrates and urea peroxide. Occasionally, it can also be expedient to shift the pH of the medium again after the activation reaction has taken place by means of suitable additives, especially in the acidic range.
- the amounts of per compounds are generally chosen so that the solutions contain between 10 ppm and 10% active oxygen, preferably between 50 and 5000 ppm active oxygen.
- the amount of activator used also depends on the application. Depending on the desired degree of activation, 0.03-1 mol, preferably 0.1-0.5 mol, of activator per mol of inorganic per-compound are used, but in special cases these limits can also be exceeded or fallen short of.
- the isatoic anhydride according to the invention or its derivatives can be used for activation in pure form or, if this is expedient, for example to increase the storage stability, in special forms of supply, such as tablets, granules or in finely divided coated form (so-called prills). Of particular importance are those granular shapes that are produced by agglomeration granulation. For the Machine dosing is suitable for solutions in organic solvents or liquid dispersions that contain the activator.
- pre-assembled agents in a mixture with the per compounds to be activated and, if appropriate, further components required for the desired bleaching or oxidation process, such as pH regulating agents and stabilizers for per compounds.
- further components required for the desired bleaching or oxidation process such as pH regulating agents and stabilizers for per compounds.
- activators can also be present. Mixing with selected amounts of per-compounds and other additives makes the application easier and the user achieves the desired result more reliably, since the optimal conditions are obtained when the agents are dissolved without further action. Such agents are therefore a further subject of the present invention.
- the activators according to the invention can be combined with almost all the usual components of detergents and bleaches. In this way it is possible to build up means which are particularly suitable for textile treatment at low temperatures and also means which are suitable in several temperature ranges up to the traditional area of cooked laundry.
- the main components of such detergents and bleaches are, besides per-compounds and activators, builders and surfactants.
- other customary auxiliaries and accompanying substances such as graying inhibitors, peroxide stabilizers, electrolytes, optical brighteners, enzymes, perfume oils, foam regulators and conditioning agents, can be present in these agents if this is expedient.
- customary builder substances are condensed phosphates, alkali silicates, alkali carbonates, salts of amino carboxylic acids, such as nitrilotriacetic acid, salts of polyphosphonic acids, such as hydroxyethane diphosphonic acid, salts of polycarboxylic acids, such as citric acid or polyacrylic acid, and insoluble sodium aluminum silicates and NaX type NaA zeolite NaA.
- Particularly suitable surfactants are those of the type of the nonionic and synthetic anionic surfactants.
- nonionic surfactants are the polyethylene glycol monoalkyl and polyethylene glycol monophenyl ethers prepared from long-chain alcohols or alkylphenols and ethylene oxide, and the long-chain alkylglycosides.
- the anionic surfactants are primarily sulfates and sulfonates of long-chain compounds, for example alkylbenzenesulfonates, fatty acid ester sulfonates, alkanesulfonates, olefin sulfonates, fatty alcohol sulfates and sulfates of polyethylene glycol monoethers. Soaps and salts of long-chain acylcyanamides can also be used.
- Typical detergents and bleaches according to the invention have approximately the following composition: 0.5 to 20% by weight, preferably 5 to 15% by weight of anionic and / or nonionic surfactants, 0.5 to 60% by weight, preferably 5 to 40% by weight, of builders from the group of condensed phosphates, alkali silicates, alkali carbonates, sodium aluminum silicates and mixtures thereof, 0 to 20% by weight, preferably 0.5 to 8% by weight, of builder substances from the group consisting of salts of aminocarboxylic acid ren, salts of polyphosphonic acids, salts of polycarboxylic acids and mixtures thereof, 2 to 35% by weight, preferably 5 to 30% by weight, of inorganic per-compounds, 0.3 to 20% by weight, preferably 1 to 10% by weight, of isatoic anhydride and / or its derivatives, ad 100% usual auxiliary and accompanying substances and water
- agents which are used as additives to peroxide-containing or peroxide-free detergents are also suitable as the form of preparation of the activators according to the invention for textile washing. They essentially contain activator or a mixture of activator and per compound and, if appropriate, further auxiliaries and additives, in particular stabilizers, pH-regulating agents, thickeners and surfactants.
- Typical bleach additives according to the invention have approximately the following composition: 5 to 50% by weight, preferably 15 to 35% by weight, of inorganic per-compound, 2 to 30% by weight, preferably 5 to 25% by weight, of isatoic anhydride and / or its derivatives, 0 to 5% by weight, preferably 0.1 to 3% by weight, of peroxide stabilizers, 0 to 40% by weight, preferably 5 to 30% by weight of pH-regulating agents, ad 100% by weight of other customary auxiliaries and additives.
- agents intended for cleaning hard surfaces contain, in particular, surfactants and framework substance zen and, in the case of polishing and abrasive agents, abrasive components. Since these agents are often used at room temperature, the use of the activators according to the invention has a particularly advantageous effect on the bleaching and germicidal action.
- Disinfectants based on the activators according to the invention generally contain, in addition to this and inorganic per-compounds, further auxiliaries and additives, such as pH-regulating substances, stabilizers and surfactants. In special cases, they can additionally contain special microbicides which increase the very broad killing effect of the activated per-compound against certain germs.
- Typical disinfectants according to the invention have approximately the following composition: 5 to 40% by weight, preferably 10 to 20% by weight, of inorganic per-compounds, 2 to 40% by weight, preferably 5 to 20% by weight, of isatoic anhydride and / or its derivatives, 0 to 5% by weight, preferably 0.1 to 3% by weight, of peroxide stabilizers, 0.1 to 20% by weight, preferably 0.2 to 5% by weight of surfactants, ad 100% by weight of other auxiliaries and additives.
- the use of the activators according to the invention is in no way limited to the use in the ready-made form of these described or other types.
- the individual dosing of reagents in the foreground since it is often the cheaper method.
- AS Acrylic acid
- CMC Carboxymethyl cellulose
- EDTA Tetrasodium salt of ethylenediaminetetraacetic acid
- EDTMP Hexasodium salt of ethylenediaminetetramethylenephosphonic acid (peroxide stabilizer)
- EO Ethylene oxide
- HEC Hydroxyethyl cellulose
- MA Maleic anhydride
- composition in percent by weight: Soap (C12-C18) 1.5 Na dodecylbenzenesulfonate 9.0 Fatty alcohol ethoxylate (C12-C18 + 10 EO) 3.5 Sodium triphosphate 20.0 Sodium silicate (3.2) 5.0 Zeolite NaA 15.0 EDTMP 0.3 MA-AS copolymer (60:40) 1.5 Sodium perborate monohydrate 18.0 Isatoic anhydride 3.0 Brightener, perfume, enzyme ad 100 Carboxymethyl cellulose, Na2SO4 and water
- the test was carried out in a launderometer, type Atlas Standard, using a phosphate-free detergent under the following conditions: Fleet volume 250 ml Fabric: 6.3 g fill fabric (white cotton) 2.1 g test fabric Water hardness: 17 ° d. H. Temperatures: 30 or 40 ° C Washing time: 30 minutes including heating up time (3 ° C / min) Rinse: 3 x 30 sec.
- Detergent composition (% by weight): Alkylbenzenesulfonate Na salt 7 Tallow alcohol + 5 EO 5.5 Na2CO3 12 Sodium silicate (3.2) 3.3 Zeolite NaA 28 EDTA 0.3 Sodium perborate tetrahydrate 28 CMC + HEC 1.5 Na2SO4 and water ad 100 Dosage: detergent 7.16 g / l Activator 143 mg / l or 1.26 mmol / l
- Table 3 contains the test results on various test soils in comparison to activators customary today (mean values from 4 tests): Table 3 Try at 24 ° C Activator Currant on cotton Red wine on refined cotton Tea on finished cotton Red wine on polyester / cotton Without perborate and activator 40.5 36.9 27.1 47.7 Isatoic anhydride 45.7 39.6 33.0 50.3 Tetraacetylethylenediamine 42.7 38.0 31.1 48.7 Sulfophenyl isononate Na salt 41.8 38.5 30.3 48.9
- the storage was carried out in a mixture with a powdered phosphate-free detergent, this mixture containing 3% by weight of activator either in pure form or in the form of agglomeration granules.
- the detergent had the following composition (in% by weight): Soap 1.5 Na dodecylbenzenesulfonate 8.0 Fatty alcohol ethoxylate 4.0 Na2CO3 8th Sodium silicate (3.2) 3.5 Zeolite NaA 25th Hydroxyethane diphosphonate (Na salt) 0.3 MA-AS copolymer (60:40) 5 Sodium perborate tetrahydrate 26 Brightener, perfume, enzyme, carboxymethyl cellulose Na2SO4 and water ad 100
- the activator granules had been prepared from the pure, powdery activators and carboxymethyl cellulose as binders according to DE 30 11 998 and contained 94% by weight of active substance.
- the mixtures containing the activators in granular form were stored in laminated cardboard boxes in a climatic cell at 30 ° C. and 80% relative humidity. The other mixtures were stored in unlaminated boxes in the laboratory. In all cases, the peracid, which formed when the mixtures were dissolved in water, was determined iodometrically at the beginning and after 4 and 8 weeks of storage under standard conditions. Table 3 contains the results in relative numbers, based on 100% peracid formation at the start of storage. The superior stability of the isatoic anhydride is evident under both storage conditions.
- composition (percent by weight) Sodium perborate monohydrate 12.0 Isatoic anhydride 12.0 Na2CO3 15.0 Na4P2O7 25.0 EDTMP 1.2 Nonylphenol ethoxylate (9 EO) 1.3 Na2SO4 and water ad 100
- the powdery agent After being dissolved in water at room temperature, the powdery agent was used in the form of a bath for instrument disinfection. When using about 4 g per liter, the necessary disinfection times were less than 60 minutes.
- Test solution detergent according to Example 2 in water at 17 ° dH, adjusted to pH 10, Dosage: Detergent: 10 g / l Activator: 150, 300 or 600 mg / l Temperature: 37 ° C Culture medium: casein peptone soybean meal peptone agar
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Abstract
Description
Anorganische Perverbindungen, insbesondere Wasserstoffperoxid und feste Perverbindungen, die sich in Wasser unter Freisetzung von Wasserstoffperoxid lösen, wie Natriumperborat und Natriumcarbonat-Perhydrat, 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 beispielsweise mit H₂O₂ oder Perborat in alkalischen Bleichflotten erst bei Temperaturen oberhalb von etwa 80 °C eine ausreichend schnelle Bleiche verschmutzter Textilien. Bei niedrigeren Temperaturen kann die Oxidationswirkung der anorganischen Perverbindungen durch Zusatz sogenannter Aktivatoren verbessert werden, für die zahlreiche Vorschläge in der Literatur bekannt geworden sind. Unter anderem wurden Carbonsäureanhydride für diesen Zweck vorgeschlagen (DE 893 049) und in Bleichmitteln verwendet (DE 19 12 579). Durch Zusatz dieser Substanzen kann die Bleichwirkung wäßriger Peroxidflotten so weit gesteigert werden, daß bereits bei 60 °C nahezu die gleichen Wirkungen wie mit der Peroxidflotte allein bei 95 °C eintreten.Inorganic per-compounds, especially hydrogen peroxide and solid per-compounds, which dissolve in water to release hydrogen peroxide, such as sodium perborate and sodium carbonate perhydrate, 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; For example, with H₂O₂ or perborate in alkaline bleaching liquors, sufficiently quick bleaching of soiled textiles can only be achieved at temperatures above about 80 ° C. At lower temperatures, the oxidation effect of the inorganic per compounds can be improved by adding so-called activators, for which numerous proposals have become known in the literature. Among other things, carboxylic anhydrides have been proposed for this purpose (DE 893 049) and used in bleaching agents (DE 19 12 579). By adding these substances, the bleaching effect of aqueous peroxide liquors can be increased to such an extent that already at 60 ° C almost the same effects occur as with the peroxide liquor alone at 95 ° C.
Im Bemühen um energiesparende Wasch- und Bleichverfahren gewinnen in den letzten Jahren auch Anwendungstemperaturen deutlich unterhalb 60 °C, insbesondere unterhalb 45 °C bis herunter zur Kaltwassertemperatur an Bedeutung.In the effort to save energy in washing and bleaching, application temperatures well below 60 ° C, in particular below 45 ° C down to the cold water temperature, have become increasingly important in recent years.
Bei diesen Temperaturen läßt die Wirkung der bekannten Aktivatoren aber bereits deutlich nach. Es hat deshalb nicht an Bestrebungen gefehlt, für diesen Temperaturbereich wirksamere Aktivatoren zu entwickeln, ohne daß bis heute ein überzeugender Erfolg zu verzeichnen gewesen wäre. Auch die vorliegende Erfindung hat die Verbesserung der Oxidations- und Bleichwirkung anorganischer Perverbindung bei niedrigen Temperaturen unterhalb von 80 °C, insbesondere im Temperaturbereich von ca. 15 bis 45 °C zum Ziel.At these temperatures, however, the effect of the known activators is already significantly reduced. There has been no shortage of efforts to develop more effective activators for this temperature range without convincing success to date. The present invention also aims to improve the oxidation and bleaching effect of inorganic per-compound at low temperatures below 80 ° C., in particular in the temperature range from approximately 15 to 45 ° C.
Es wurde nun gefunden, daß bei Verwendung von Isatosäureanhydrid oder einigen seiner Derivate als Aktivatoren in diesem Temperaturbereich eine außerordentliche Steigerung der Oxidations- und Bleichwirkung anorganischer Perverbindungen in Oxidations-, Bleich- und Waschflotten erreicht wird. Es handelt sich bei diesen Aktivatoren um Verbindungen mit der Formel
R = Methyl, Ethyl, n-Propyl, iso-Propyl, n-Butyl, iso-Butyl, Propenyl, Butenyl, Cyclohexyl, Phenyl oder Benzyl;
X = Methyl, Methoxy, Chlor, Brom oder SO₃⊖;
n = 0,1 oder 2.It has now been found that when isatoic anhydride or some of its derivatives are used as activators in this temperature range, there is an extraordinary increase in the oxidation and bleaching action of inorganic per compounds in oxidation, bleaching and washing liquors. These activators are compounds with the formula
R = methyl, ethyl, n-propyl, iso-propyl, n-butyl, iso-butyl, propenyl, butenyl, cyclohexyl, phenyl or benzyl;
X = methyl, methoxy, chlorine, bromine or SO₃ ⊖ ;
n = 0.1 or 2.
Auch diese Verbindungen sind zum Teil an sich bekannt und käuflich, oder sie können analog zu den bekannten Verbindungen synthetisiert werden (siehe DE 499 822 und Beilsteins Handbuch der organischen Chemie, Band 27, System-Nummer 4298, Hauptwerk und 1. bis 4. Ergänzungswerk).Some of these compounds are known per se and are commercially available, or they can be synthesized analogously to the known compounds (see DE 499 822 and Beilstein's Handbook of Organic Chemistry, volume 27, system number 4298, main work and 1st to 4th supplementary work ).
Bevorzugt werden von diesen Verbindungen die im Benzolring nicht substituierten Vertreter (n = 0), in denen R einen der Reste Methyl, Ethyl, n-Propyl oder iso-Propyl darstellt. Besonders bevorzugt wird das nicht substituierte Isatosäureanhydrid (R = H, n = 0).Of these compounds, preference is given to the representatives (n = 0) in the benzene ring which are not substituted and in which R represents one of the radicals methyl, ethyl, n-propyl or isopropyl. The unsubstituted isatoic anhydride (R = H, n = 0) is particularly preferred.
Bei dem erfindungsgemäßen Verfahren können Isatosäureanhydrid und seine Derivate als Aktivatoren überall dort eingesetzt werden, wo es auf eine besondere Steigerung der Oxidationswirkung anorganischer Perverbindungen bei niedrigen Temperaturen ankommt, z. B. bei der Bleiche von Textilien, Haaren oder harten Oberflächen, bei der Oxidation organischer oder anorganischer Zwischenprodukte und bei der Desinfektion. Dabei übertreffen die meisten dieser Aktivatoren in ihren Eigenschaften die besten bisher bekannten Carbonsäureanhydridaktivatoren bei weitem.In the process according to the invention, isatoic anhydride and its derivatives can be used as activators wherever a particular increase in the oxidation activity of inorganic per-compounds is important at low temperatures, for. B. in the bleaching of textiles, hair or hard surfaces, in the oxidation of organic or inorganic intermediates and in disinfection. Most of these activators far outperform the best carbonic anhydride activators known to date.
Die erfindungsgemäße Verwendung besteht darin, Bedingungen zu schaffen, unter denen Wasserstoffperoxid und Isatosäureanhydrid bzw. seine Derivate miteinander reagieren können, mit dem Ziel, stärker oxidierend wirkende Folgeprodukte zu erhalten. Solche Bedingungen liegen insbesondere dann vor, wenn beide Reaktionspartner in wäßriger alkalischer Lösung aufeinander treffen.The use according to the invention is to create conditions under which hydrogen peroxide and isatoic anhydride or its derivatives can react with one another with the aim of obtaining secondary products which have a stronger oxidizing action. Such conditions exist in particular when the two reactants meet in an aqueous alkaline solution.
Je nach Verwendungszweck können die Bedingungen weit variiert werden. So kommen neben rein wäßrigen Lösungen auch Mischungen aus Wasser und geeigneten organischen Lösungsmitteln, z. B. für die Anwendung in der Desinfektion oder bei der Oxidation von Zwischenprodukten, als Reaktionsmedium in Frage. Der pH-Wert des Reaktionsmediums kann in weiten Grenzen, vom schwach sauren Bereich (pH 4) bis in den stark alkalischen Bereich (pH 13), je nach Anwendungszweck gewählt werden. Bevorzugt wird der alkalische Bereich von pH 8 bis pH 11, da er für die Aktivierungsreaktion und die Stabilität der gebildeten Perverbindung besonders vorteilhaft ist. Aus diesem Grunde wird der erfindungsgemäße Aktivator auch bevorzugt zusammen mit einem Natriumperborat oder mit Natriumcarbonat-Perhydrat verwendet, die in ihren Lösungen bereits pH-Werte dieses Bereichs aufweisen. Beispiele anderer geeigneter Perverbindungen sind Phosphat-Perhydrate und Harnstoffperoxid. Gelegentlich kann es auch zweckmäßig sein, den pH-Wert des Mediums nach erfolgter Aktivierungsreaktion durch geeignete Zusätze nochmals, vor allem in den sauren Bereich, zu verschieben. Die Einsatzmengen an Perverbindungen werden im allgemeinen so gewählt, daß in den Lösungen zwischen 10 ppm und 10 % Aktivsauerstoff, vorzugsweise zwischen 50 und 5000 ppm Aktivsauerstoff vorhanden sind. Auch die verwendete Menge an Aktivator hängt vom Anwendungszweck ab. Je nach gewünschtem Aktivierungsgrad werden 0,03 - 1 Mol, vorzugsweise 0,1 - 0,5 Mol Aktivator pro Mol anorganischer Perverbindung verwendet, doch können in besonderen Fällen diese Grenzen auch über- oder unterschritten werden.The conditions can be varied widely depending on the intended use. In addition to purely aqueous solutions, mixtures of water and suitable organic solvents, e.g. B. for the use in disinfection or in the oxidation of intermediates as a reaction medium in question. The pH of the reaction medium can be selected within wide limits, from the weakly acidic range (pH 4) to the strongly alkaline range (pH 13), depending on the application. The alkaline range from pH 8 to pH 11 is preferred since it is particularly advantageous for the activation reaction and the stability of the per compound formed. For this reason, the activator according to the invention is also preferably used together with a sodium perborate or with sodium carbonate perhydrate, which already have pH values of this range in their solutions. Examples of other suitable per compounds are phosphate perhydrates and urea peroxide. Occasionally, it can also be expedient to shift the pH of the medium again after the activation reaction has taken place by means of suitable additives, especially in the acidic range. The amounts of per compounds are generally chosen so that the solutions contain between 10 ppm and 10% active oxygen, preferably between 50 and 5000 ppm active oxygen. The amount of activator used also depends on the application. Depending on the desired degree of activation, 0.03-1 mol, preferably 0.1-0.5 mol, of activator per mol of inorganic per-compound are used, but in special cases these limits can also be exceeded or fallen short of.
Das erfindungsgemäße Isatosäureanhydrid bzw. seine Derivate können zur Aktivierung in reiner Form oder, wenn dies, beispielsweise zur Erhöhung der Lagerstabilität, zweckmäßig ist, in speziellen Anbietungsformen, wie Tabletten, Granulaten oder in feinteiliger umhüllter Form (sogenannte Prills), eingesetzt werden. Besonderer Bedeutung kommt dabei solchen körnigen Formen zu, die durch Agglomerationsgranulation hergestellt werden. Für die maschinelle Dosierung eignen sich Lösungen in organischen Lösungsmitteln oder flüssige Dispersionen, die den Aktivator enthalten.The isatoic anhydride according to the invention or its derivatives can be used for activation in pure form or, if this is expedient, for example to increase the storage stability, in special forms of supply, such as tablets, granules or in finely divided coated form (so-called prills). Of particular importance are those granular shapes that are produced by agglomeration granulation. For the Machine dosing is suitable for solutions in organic solvents or liquid dispersions that contain the activator.
Bevorzugt erfolgt der Einsatz in vorkonfektionierten Mitteln im Gemisch mit den zu aktivierenden Perverbindungen und gegebenenfalls weiteren, für den gewünschten Bleich- oder Oxidationsprozeß erforderlichen Komponenten, wie pH-regulierenden Mitteln und Stabilisatoren für Perverbindungen. Dabei können neben Isatosäureanhydrid und/oder seinen Derivaten auch andere Aktivatoren zugegen sein. Durch die Abmischung mit ausgesuchten Mengen an Perverbindungen und weiteren Zusatzstoffen wird die Anwendung erleichtert und der Anwender erzielt sicherer das gewünschte Ergebnis, da sich beim Auflösen der Mittel ohne weiteres Zutun die optimalen Bedingungen einstellen. Derartige Mittel sind deshalb ein weiterer Gegenstand der vorliegenden Erfindung.It is preferably used in pre-assembled agents in a mixture with the per compounds to be activated and, if appropriate, further components required for the desired bleaching or oxidation process, such as pH regulating agents and stabilizers for per compounds. In addition to isatoic anhydride and / or its derivatives, other activators can also be present. Mixing with selected amounts of per-compounds and other additives makes the application easier and the user achieves the desired result more reliably, since the optimal conditions are obtained when the agents are dissolved without further action. Such agents are therefore a further subject of the present invention.
Auf dem Gebiet der Textilwäsche können die erfindungsgemäßen Aktivatoren mit nahezu allen üblichen Bestandteilen von Wasch- und Bleichmitteln kombiniert werden. Man kann auf diese Weise Mittel aufbauen, die sich speziell zur Textilbehandlung bei niedrigen Temperaturen eignen und auch solche, die in mehreren Temperaturbereichen bis hinauf zum traditionellen Bereich der Kochwäsche geeignet sind.In the field of textile washing, the activators according to the invention can be combined with almost all the usual components of detergents and bleaches. In this way it is possible to build up means which are particularly suitable for textile treatment at low temperatures and also means which are suitable in several temperature ranges up to the traditional area of cooked laundry.
Hauptbestandteile solcher Wasch- und Bleichmittel sind, neben Perverbindungen und Aktivator, Gerüstsubstanzen (Builders) und Tenside. Daneben können andere übliche Hilfsstoffe und Begleitstoffe, wie Vergrauungsinhibitoren, Peroxidstabilisatoren, Elektrolyte, optische Aufheller, Enzyme, Parfümöle, Schaumregulatoren und avivierende Substanzen in diesen Mitteln vorliegen, wenn dies zweckmäßig ist.The main components of such detergents and bleaches are, besides per-compounds and activators, builders and surfactants. In addition, other customary auxiliaries and accompanying substances, such as graying inhibitors, peroxide stabilizers, electrolytes, optical brighteners, enzymes, perfume oils, foam regulators and conditioning agents, can be present in these agents if this is expedient.
Beispiele üblicher Gerüstsubstanzen sind kondensierte Phosphate, Alkalisilikate, Alkalicarbonate, Salze von Aminocarbonsäuren, wie Nitrilotriessigsäure, Salze von Polyphosphonsäuren, wie Hydroxyethandiphosphonsäure, Salze von Polycarbonsäuren, wie Citronensäure oder Polyacrylsäure und unlösliche Natriumaluminiumsilikate vom Typ Zeolith NaA und NaX.Examples of customary builder substances are condensed phosphates, alkali silicates, alkali carbonates, salts of amino carboxylic acids, such as nitrilotriacetic acid, salts of polyphosphonic acids, such as hydroxyethane diphosphonic acid, salts of polycarboxylic acids, such as citric acid or polyacrylic acid, and insoluble sodium aluminum silicates and NaX type NaA zeolite NaA.
Als Tenside kommen insbesondere solche vom Typ der nichtionischen und synthetischen anionischen Tenside in Frage. Beispiele für nichtionische Tenside sind die aus langkettigen Alkoholen oder Alkylphenolen und Ethylenoxid hergestellten Polyethylenglykolmonoalkyl- und Polyethylenglykolmonophenylether sowie die langkettigen Alkylglycoside.Particularly suitable surfactants are those of the type of the nonionic and synthetic anionic surfactants. Examples of nonionic surfactants are the polyethylene glycol monoalkyl and polyethylene glycol monophenyl ethers prepared from long-chain alcohols or alkylphenols and ethylene oxide, and the long-chain alkylglycosides.
Bei den anionischen Tensiden handelt es sich in erster Linie um Sulfate und Sulfonate langkettiger Verbindungen, beispielsweise Alkylbenzolsulfonate, Fettsäureestersulfonate, Alkansulfonate, Olefinsulfonate, Fettalkoholsulfate und Sulfate von Polyethylenglykolmonoethern. Weiterhin können Seifen und Salze langkettiger Acylcyanamide verwendet werden.The anionic surfactants are primarily sulfates and sulfonates of long-chain compounds, for example alkylbenzenesulfonates, fatty acid ester sulfonates, alkanesulfonates, olefin sulfonates, fatty alcohol sulfates and sulfates of polyethylene glycol monoethers. Soaps and salts of long-chain acylcyanamides can also be used.
Typische Wasch- und Bleichmittel gemäß der Erfindung haben etwa folgende Zusammensetzung:
0,5 bis 20 Gew.-%, vorzugsweise 5 bis 15 Gew.-% anionische und/oder nichtionische Tenside,
0,5 bis 60 Gew.-%, vorzugsweise 5 bis 40 Gew.-% Gerüstsubstanzen aus der Gruppe kondensierte Phosphate, Alkalisilikate, Alkalicarbonate, Natriumaluminiumsilikate und deren Mischungen,
0 bis 20 Gew.-%, vorzugsweise 0,5 bis 8 Gew.-% Gerüstsubstanzen aus der Gruppe Salze von Aminocarbonsäu ren, Salze von Polyphosphonsäuren, Salze von Polycarbonsäuren und deren Mischungen,
2 bis 35 Gew.-%, vorzugsweise 5 bis 30 Gew.-% anorganische Perverbindungen,
0,3 bis 20 Gew.-%, vorzugsweise 1 bis 10 Gew.-% Isatosäureanhydrid und/oder seine Derivate,
ad 100% übliche Hilfs- und Begleitstoffe und WasserTypical detergents and bleaches according to the invention have approximately the following composition:
0.5 to 20% by weight, preferably 5 to 15% by weight of anionic and / or nonionic surfactants,
0.5 to 60% by weight, preferably 5 to 40% by weight, of builders from the group of condensed phosphates, alkali silicates, alkali carbonates, sodium aluminum silicates and mixtures thereof,
0 to 20% by weight, preferably 0.5 to 8% by weight, of builder substances from the group consisting of salts of aminocarboxylic acid ren, salts of polyphosphonic acids, salts of polycarboxylic acids and mixtures thereof,
2 to 35% by weight, preferably 5 to 30% by weight, of inorganic per-compounds,
0.3 to 20% by weight, preferably 1 to 10% by weight, of isatoic anhydride and / or its derivatives,
ad 100% usual auxiliary and accompanying substances and water
Neben kombinierten Wasch- und Bleichmitteln kommen als Konfektionierungsform der erfindungsgemäßen Aktivatoren für die Textilwäsche auch Mittel in Betracht, die als Zusätze zu peroxidhaltigen oder peroxidfreien Waschmitteln angewendet werden. Sie enthalten im wesentlichen Aktivator bzw. ein Gemisch aus Aktivator und Perverbindung sowie gegebenenfalls weitere Hilfs- und Zusatzstoffe, insbesondere Stabilisatoren, pH-regulierende Mittel, Verdickungsmittel und Tenside.In addition to combined detergents and bleaches, agents which are used as additives to peroxide-containing or peroxide-free detergents are also suitable as the form of preparation of the activators according to the invention for textile washing. They essentially contain activator or a mixture of activator and per compound and, if appropriate, further auxiliaries and additives, in particular stabilizers, pH-regulating agents, thickeners and surfactants.
Typische Bleichzusatzmittel gemäß der Erfindung haben etwa folgende Zusammensetzung:
5 bis 50 Gew.-%, vorzugsweise 15 bis 35 Gew.-% anorganische Perverbindung,
2 bis 30 Gew.-%, vorzugsweise 5 bis 25 Gew.-% Isatosäureanhydrid und/oder seine Deriavte,
0 bis 5 Gew.-%, vorzugsweise 0,1 bis 3 Gew.-% Peroxidstabilisatoren,
0 bis 40 Gew.-%, vorzugsweise 5 bis 30 Gew.-% pH-regulierende Mittel,
ad 100 Gew.-% andere übliche Hilfs- und Zusatzstoffe.Typical bleach additives according to the invention have approximately the following composition:
5 to 50% by weight, preferably 15 to 35% by weight, of inorganic per-compound,
2 to 30% by weight, preferably 5 to 25% by weight, of isatoic anhydride and / or its derivatives,
0 to 5% by weight, preferably 0.1 to 3% by weight, of peroxide stabilizers,
0 to 40% by weight, preferably 5 to 30% by weight of pH-regulating agents,
ad 100% by weight of other customary auxiliaries and additives.
Zur Reinigung harter Oberflächen bestimmte Mittel enthalten neben perverbindung und Aktivator insbesondere Tenside, Gerüstsubstan zen und, im Falle von Polier- und Scheuermitteln, abrasiv wirkende Bestandteile. Da diese Mittel häufig bei Raumtemperatur angewendet werden, wirkt sich hier die Verwendung der erfindungsgemäßen Aktivatoren besonders vorteilhaft auf die bleichende und keimtötende Wirkung aus.In addition to per compound and activator, agents intended for cleaning hard surfaces contain, in particular, surfactants and framework substance zen and, in the case of polishing and abrasive agents, abrasive components. Since these agents are often used at room temperature, the use of the activators according to the invention has a particularly advantageous effect on the bleaching and germicidal action.
Besondere Bedeutung besitzen konfektionierte Mittel bei der Anwendung in der Desinfektion, da hier im allgemeinen erhöhte Anforderungen an die Anwendungssicherheit gestellt werden. Desinfektionsmittel auf Basis der erfindungsgemäßen Aktivatoren enthalten neben diesem und anorganischen Perverbindungen im allgemeinen noch weitere Hilfs- und Zusatzstoffe, wie pH-regulierende Substanzen, Stabilisatoren und Tenside. In besondere Fällen können sie spezielle Mikrobizide zusätzlich enthalten, die die an sich sehr breite abtötende Wirkung der aktivierten Perverbindung gegenüber bestimmten Keimen verstärken.Ready-made agents are of particular importance for use in disinfection, since there are generally increased demands on application safety. Disinfectants based on the activators according to the invention generally contain, in addition to this and inorganic per-compounds, further auxiliaries and additives, such as pH-regulating substances, stabilizers and surfactants. In special cases, they can additionally contain special microbicides which increase the very broad killing effect of the activated per-compound against certain germs.
Typische Desinfektionsmittel gemäß der Erfindung haben etwa folgende Zusammensetzung:
5 bis 40 Gew.-%, vorzugsweise 10 bis 20 Gew.-% anorganische Perverbindungen,
2 bis 40 Gew.-%, vorzugsweise 5 bis 20 Gew.-% Isatosäureanhydrid und/oder seine Derivate,
0 bis 5 Gew.-%, vorzugsweise 0,1 bis 3 Gew.-% Peroxidstabilisatoren,
0,1 bis 20 Gew.-%, vorzugsweise 0,2 bis 5 Gew.-% Tenside,
ad 100 Gew.-% weitere Hilfs- und Zusatzstoffe.Typical disinfectants according to the invention have approximately the following composition:
5 to 40% by weight, preferably 10 to 20% by weight, of inorganic per-compounds,
2 to 40% by weight, preferably 5 to 20% by weight, of isatoic anhydride and / or its derivatives,
0 to 5% by weight, preferably 0.1 to 3% by weight, of peroxide stabilizers,
0.1 to 20% by weight, preferably 0.2 to 5% by weight of surfactants,
ad 100% by weight of other auxiliaries and additives.
Die erfindungsgemäße Verwendung der Aktivatoren ist aber keinesfalls auf die Anwendung in konfektionierter Form dieser geschilderten oder anderer Arten beschränkt. So steht beispielsweise im gewerblichen Bereich im allgemeinen die Einzeldosierung von Reagenzien im Vordergrund, da sie oft das kostengünstigere Verfahren darstellt.However, the use of the activators according to the invention is in no way limited to the use in the ready-made form of these described or other types. For example, in in the commercial field in general, the individual dosing of reagents in the foreground, since it is often the cheaper method.
Die verwendeten Abkürzungen haben folgende Bedeutung:
Bei Anwendungskonzentration von 5 bis 10 g/l wurden mit diesem Mittel bei Waschtemperaturen von 20 bis 95 °C hervorragende Bleichergebnisse erzielt.At application concentrations of 5 to 10 g / l were with this Excellent bleaching results achieved at washing temperatures of 20 to 95 ° C.
Die Prüfung erfolgte im Launderometer, Typ Atlas Standard, unter Verwendung eines phosphatfreien Waschmittels bei folgenden Bedingungen:
Flottenvolumen 250 ml
Gewebe: 6,3 g Füllgewebe (weiße Baumwolle)
2,1 g Testgewebe
Wasserhärte: 17 ° d. H.
Temperaturen: 30 oder 40 °C
Waschzeit: 30 Minuten einschließlich Aufheizzeit (3 °C/min)
Spülen: 3 x 30 sec.
Aktivator 143 mg/l oder 1,26 mMol/lThe test was carried out in a launderometer, type Atlas Standard, using a phosphate-free detergent under the following conditions:
Fleet volume 250 ml
Fabric: 6.3 g fill fabric (white cotton)
2.1 g test fabric
Water hardness: 17 ° d. H.
Temperatures: 30 or 40 ° C
Washing time: 30 minutes including heating up time (3 ° C / min)
Rinse: 3 x 30 sec.
Activator 143 mg / l or 1.26 mmol / l
Die Auswertung der Versuche wurde durch Remissionsmessung an den getrockneten Geweben vorgenommen. Die Ergebnisse, die in den folgenden Tabellen zusammengefaßt sind, stellen die Remissionswerte in % dar, bezogen auf BaSO₄ = 100, die bei einer Wellenlänge von 460 nm gemessen wurden. Höhere Werte zeigen helleres Gewebe an.
Aus den Remissionswerten wird deutlich, daß mit Isatosäureanhydrid bei beiden Temperaturen eine sehr viel stärkere Aktivierung des Perborats als mit herkömmlichen Anhydridaktivatoren erreicht wird.It is clear from the reflectance values that with isatoic anhydride a much stronger activation of the perborate is achieved at both temperatures than with conventional anhydride activators.
Ähnlich gute Ergebnisse wurden bei Verwendung von N-Methylisatosäureanhydrid erhalten.Similar good results were obtained using N-methylisatoic anhydride.
Die Prüfung erfolgte in einer Drehflügelwaschmaschine vom Typ Whirlpool unter Verwendung des phosphathaltigen Waschmittels Tide bei folgenden Bedingungen:
Flottenvolumen: 65 l
Gewebe: 2,3 kg Füllgewebe (weiße Baumwolle)
+ 8 Testanschmutzungen (je 1 Lappen von 2,1 g)
Wasserhärte: 5,6 °dH (99 mg CaCO₃, Ca : Mg = 3 : 1)
Waschzeit: 14 Minuten
Temperatur: 24 °C (cold wash)
Dosierung: 1,35 g Waschmittel
(pro Liter) + 67,5 mg Perboratmonohydrat
+ 54 mg AktivatorThe test was carried out in a whirlpool type washing machine using the phosphate-containing detergent Tide under the following conditions:
Fleet volume: 65 l
Fabric: 2.3 kg fill fabric (white cotton)
+ 8 test stains (1 cloth of 2.1 g each)
Water hardness: 5.6 ° dH (99 mg CaCO₃, Ca: Mg = 3: 1)
Washing time: 14 minutes
Temperature: 24 ° C (cold wash)
Dosage: 1.35 g detergent
(per liter) + 67.5 mg perborate monohydrate
+ 54 mg activator
Die Auswertung erfolgte durch Remissionsmessung wie in Beispiel 2. Tabelle 3 enthält die Versuchsergebnisse an verschiedenen Testanschmutzungen im Vergleich zu heute üblichen Aktivatoren (Mittelwerte aus 4 Versuchen):
Die Ergebnisse zeigen, daß Isatosäureanhydrid auch unter US-amerikanischen Waschbedingungen vorteilhaft eingesetzt werden kann.The results show that isatoic anhydride can also be used advantageously under US washing conditions.
Eine ähnliche Steigerung der Oxidationswirkung anorganischer Perverbindungen erzielt man auch auf anderen Anwendungsgebieten.A similar increase in the oxidation effect of inorganic per compounds is also achieved in other areas of application.
Die Lagerung erfolgte in Mischung mit einem pulverförmigen phsophatfreien Waschmittel, wobei diese Mischung 3 Gew.-% an Aktivator entweder in reiner Form oder in Form von Agglomerationsgranulat enthielt.
Die Aktivatorgranulate waren aus den reinen, pulverförmigen Aktivatoren und Carboxymethylcellulose als Bindemittel gemäß DE 30 11 998 hergestellt worden und enthielten 94 Gew.-% Aktivsubstanz.The activator granules had been prepared from the pure, powdery activators and carboxymethyl cellulose as binders according to DE 30 11 998 and contained 94% by weight of active substance.
Die Lagerung der Mischungen, die die Aktivatoren in granulierter Form enthielten, erfolgte in kaschierten Kartons in einer Klimazelle bei 30 °C und 80 % relativer Feuchte. Die anderen Mischungen wurden in unkaschierten Kartons im Labor gelagert. In allen Fällen wurde zu Beginn, sowie nach 4 und 8 Wochen Lagerzeit jodometrisch die Persäure bestimmt, die sich beim Auflösen der Mischungen in Wasser unter Standardbedingungen bildete. Tabelle 3 enthält die Ergebnisse in relativen Zahlen, bezogen auf 100 % Persäurebildung zu Beginn der Lagerung. Bei beiden Lagerbedingungen zeigt sich die überlegene Stabilität des Isatosäureanhydrids.
Das pulverförmige Mittel wurde nach dem Auflösen im Wasser bei Raumtemperatur in Form eines Bades zur Instrumentendesinfektion eingesetzt. Bei Einsatzmengen von etwa 4 g pro Liter betrugen die notwendigen Desinfektionszeiten weniger als 60 Minuten.After being dissolved in water at room temperature, the powdery agent was used in the form of a bath for instrument disinfection. When using about 4 g per liter, the necessary disinfection times were less than 60 minutes.
Diese Prüfung wurde im sogenannten qualitativen Suspensionsversuch gemäß den Richtlinien für die Prüfung und Bewertung chemischer Desinfektionsverfahren der Deutschen Gesellschaft für Hygiene und Mikrobiologie (DGHM), Stand 1981, ausgeführt. Bei diesem Test werden je 10 ml der zu prüfenden Desinfektionsmittelverdünnung mit 0,1 ml einer Keimsuspension (10⁷ - 10⁸ Keime/ml) bei 20 °C gut vermischt. Nach Einwirkungszeiten von 5, 15, 30 und 60 Minuten werden jeweils 0,1 ml dieser Mischungen entnommen und in 10 ml eines Kulturmediums geimpft. Durch Bebrüten dieser Subkulturen bei 37 °C (72 h) wird geprüft, ob noch vermehrungsfähige Keime vorhanden sind.
Prüflösung: Waschmittel gemäß Beispiel 2 in Wasser von 17 °dH, auf pH 10 eingestellt,
Dosierung: Waschmittel: 10 g/l
Aktivator: 150, 300 oder 600 mg/l
Temperatur: 37 °C
Kulturmedium: Caseinpepton-Sojabohnenmehlpepton-AgarThis test was carried out in the so-called qualitative suspension test in accordance with the guidelines for the testing and evaluation of chemical disinfection processes of the German Society for Hygiene and Microbiology (DGHM), status 1981. In this test, 10 ml of the disinfectant dilution to be tested are mixed well with 0.1 ml of a germ suspension (10⁷ - 10⁸ germs / ml) at 20 ° C. After exposure times of 5, 15, 30 and 60 minutes, 0.1 ml of these mixtures are removed and inoculated in 10 ml of a culture medium. By incubating these subcultures at 37 ° C (72 h), it is checked whether germs capable of reproduction are still present.
Test solution: detergent according to Example 2 in water at 17 ° dH, adjusted to pH 10,
Dosage: Detergent: 10 g / l
Activator: 150, 300 or 600 mg / l
Temperature: 37 ° C
Culture medium: casein peptone soybean meal peptone agar
Die Ergebnisse mit vier Testkeimen sind in der folgenden Tabelle als maximale Abtötungszeiten in Minuten angegeben:
Auch aus diesen Daten wird die hervorragende Aktivierungswirkung der erfindungsgemäßen Aktivatoren deutlich.The excellent activation effect of the activators according to the invention is also evident from these data.
Claims (13)
0,5 bis 20 Gew.-%, vorzugsweise 5 bis 15 Gew.-% anionische und/oder nichtionische Tenside,
0,5 bis 6o Gew.-%, vorzugsweise 5 bis 40 Gew.-% Gerüstsubstanzen aus der Gruppe kondensierte Phosphate, Alkalisilikate, Alkalicarbonate, Natriumaluminiumsilikate und deren Mischungen,
0 bis 20 Gew.-%, vorzugsweise 0,5 bis 8 Gew.-% Gerüstsubstanzen aus der Gruppe Salze von Aminocarbonsäuren, Salze von Polyphosphonsäuren, Salze von Polycarbonsäuren und deren Mischungen,
2 bis 35 Gew.-%, vorzugsweise 5 bis 30 Gew.-% anorganische Perverbindungen,
0,3 bis 20 Gew.-%, vorzugsweise 1 bis 10 Gew.-% Aktivator,
ad 100 % übliche Hilfs- und Begleitstoffe und Wasser.11. washing and bleaching agent according to claim 6, consisting of:
0.5 to 20% by weight, preferably 5 to 15% by weight of anionic and / or nonionic surfactants,
0.5 to 60% by weight, preferably 5 to 40% by weight, of builders from the group of condensed phosphates, alkali silicates, alkali carbonates, sodium aluminum silicates and mixtures thereof,
0 to 20% by weight, preferably 0.5 to 8% by weight, of builder substances from the group salts of aminocarboxylic acids, salts of polyphosphonic acids, salts of polycarboxylic acids and mixtures thereof,
2 to 35% by weight, preferably 5 to 30% by weight, of inorganic per-compounds,
0.3 to 20% by weight, preferably 1 to 10% by weight of activator,
ad 100% usual auxiliary and accompanying substances and water.
5 bis 50 Gew.-%, vorzugsweise 15 bis 35 Gew.-% anorganische Perverbindung,
2 bis 30 Gew.-%, vorzugsweise 5 bis 25 Gew.-% Aktivator,
0 bis 5 Gew.-%, vorzugsweise 0,1 bis 3 Gew.-% Peroxidstabilisatoren,
0 bis 40 Gew.-%, vorzugsweise 5 bis 30 Gew.-% pH-regulierende Mittel,
ad 100 Gew.-% andere übliche Hilfs- und Zusatzstoffe.12. Bleach additive according to claim 6, consisting of:
5 to 50% by weight, preferably 15 to 35% by weight, of inorganic per-compound,
2 to 30% by weight, preferably 5 to 25% by weight of activator,
0 to 5% by weight, preferably 0.1 to 3% by weight, of peroxide stabilizers,
0 to 40% by weight, preferably 5 to 30% by weight of pH-regulating agents,
ad 100% by weight of other customary auxiliaries and additives.
5 bis 40 Gew.-%, vorzugsweise 10 bis 20 Gew.-% anorganische Perverbindungen,
2 bis 40 Gew.-%, vorzugsweise 5 bis 20 Gew.-% Aktivator,
0 bis 5 Gew.-%, vorzugsweise 0,1 bis 3 Gew.-% Peroxidstabilisatoren,
0,1 bis 20 Gew.-%, vorzugsweise 0,2 bis 5 Gew.-% Tenside,
ad 100 Gew.-% weitere Hilfs- und Zusatzstoffe.13. Disinfectant according to claim 6, consisting of:
5 to 40% by weight, preferably 10 to 20% by weight, of inorganic per-compounds,
2 to 40% by weight, preferably 5 to 20% by weight of activator,
0 to 5% by weight, preferably 0.1 to 3% by weight, of peroxide stabilizers,
0.1 to 20% by weight, preferably 0.2 to 5% by weight of surfactants,
ad 100% by weight of other auxiliaries and additives.
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
DE3807921 | 1988-03-10 | ||
DE3807921A DE3807921A1 (en) | 1988-03-10 | 1988-03-10 | ACTIVATOR FOR INORGANIC PERCENTAGES |
Publications (1)
Publication Number | Publication Date |
---|---|
EP0332050A1 true EP0332050A1 (en) | 1989-09-13 |
Family
ID=6349358
Family Applications (2)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
EP89902941A Pending EP0409846A1 (en) | 1988-03-10 | 1989-03-02 | Activators for inorganic percompounds |
EP89103637A Ceased EP0332050A1 (en) | 1988-03-10 | 1989-03-02 | Activators for inorganic per compounds |
Family Applications Before (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
EP89902941A Pending EP0409846A1 (en) | 1988-03-10 | 1989-03-02 | Activators for inorganic percompounds |
Country Status (6)
Country | Link |
---|---|
EP (2) | EP0409846A1 (en) |
JP (1) | JPH03503292A (en) |
KR (1) | KR900070586A (en) |
DE (1) | DE3807921A1 (en) |
DK (1) | DK188290A (en) |
WO (1) | WO1989008696A1 (en) |
Cited By (7)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
EP0482807A1 (en) * | 1990-10-23 | 1992-04-29 | WARWICK INTERNATIONAL GROUP LIMITED (Co. n 2864019) | Releasably encapsulated active substrates |
EP0482806A1 (en) * | 1990-10-23 | 1992-04-29 | WARWICK INTERNATIONAL GROUP LIMITED (Co. n 2864019) | Bleach activator formulations |
WO1993016161A1 (en) * | 1992-02-05 | 1993-08-19 | Basf Aktiengesellschaft | Granular bleaching activator composition with variously shaped grains |
WO1996004244A1 (en) * | 1994-08-05 | 1996-02-15 | Warwick International Group Limited | Bleach activators |
US5985815A (en) * | 1993-11-25 | 1999-11-16 | Warwick International Group Limited | Bleach activators |
US6930054B2 (en) | 2001-08-09 | 2005-08-16 | Cheil Industries, Inc. | Slurry composition for use in chemical mechanical polishing of metal wiring |
US6953389B2 (en) | 2001-08-09 | 2005-10-11 | Cheil Industries, Inc. | Metal CMP slurry compositions that favor mechanical removal of oxides with reduced susceptibility to micro-scratching |
Families Citing this family (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
DE4024759A1 (en) * | 1990-08-03 | 1992-02-06 | Henkel Kgaa | BLEACH ACTIVATORS IN GRANULATE FORM |
Citations (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
DE2124833A1 (en) * | 1971-05-19 | 1972-12-14 | Henkel & Cie GmbH, 4000 Dusseldorf | Scouring powder - contg per cpds and diacylated 2,5 diketopiperazines |
FR2346444A1 (en) * | 1976-04-02 | 1977-10-28 | Henkel & Cie Gmbh | OXIDIZING, BLEACHING AND WASHING PRODUCTS CONTAINING URACILS AS BLEACHING ACTIVATORS |
-
1988
- 1988-03-10 DE DE3807921A patent/DE3807921A1/en not_active Withdrawn
-
1989
- 1989-03-02 WO PCT/EP1989/000210 patent/WO1989008696A1/en not_active Application Discontinuation
- 1989-03-02 EP EP89902941A patent/EP0409846A1/en active Pending
- 1989-03-02 KR KR1019890702113A patent/KR900070586A/en not_active Application Discontinuation
- 1989-03-02 JP JP1502726A patent/JPH03503292A/en active Pending
- 1989-03-02 EP EP89103637A patent/EP0332050A1/en not_active Ceased
-
1990
- 1990-08-07 DK DK188290A patent/DK188290A/en unknown
Patent Citations (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
DE2124833A1 (en) * | 1971-05-19 | 1972-12-14 | Henkel & Cie GmbH, 4000 Dusseldorf | Scouring powder - contg per cpds and diacylated 2,5 diketopiperazines |
FR2346444A1 (en) * | 1976-04-02 | 1977-10-28 | Henkel & Cie Gmbh | OXIDIZING, BLEACHING AND WASHING PRODUCTS CONTAINING URACILS AS BLEACHING ACTIVATORS |
Cited By (8)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
EP0482807A1 (en) * | 1990-10-23 | 1992-04-29 | WARWICK INTERNATIONAL GROUP LIMITED (Co. n 2864019) | Releasably encapsulated active substrates |
EP0482806A1 (en) * | 1990-10-23 | 1992-04-29 | WARWICK INTERNATIONAL GROUP LIMITED (Co. n 2864019) | Bleach activator formulations |
WO1993016161A1 (en) * | 1992-02-05 | 1993-08-19 | Basf Aktiengesellschaft | Granular bleaching activator composition with variously shaped grains |
US5985815A (en) * | 1993-11-25 | 1999-11-16 | Warwick International Group Limited | Bleach activators |
WO1996004244A1 (en) * | 1994-08-05 | 1996-02-15 | Warwick International Group Limited | Bleach activators |
US5840667A (en) * | 1994-08-05 | 1998-11-24 | Warwick International Group, Ltd. | Bleach activators |
US6930054B2 (en) | 2001-08-09 | 2005-08-16 | Cheil Industries, Inc. | Slurry composition for use in chemical mechanical polishing of metal wiring |
US6953389B2 (en) | 2001-08-09 | 2005-10-11 | Cheil Industries, Inc. | Metal CMP slurry compositions that favor mechanical removal of oxides with reduced susceptibility to micro-scratching |
Also Published As
Publication number | Publication date |
---|---|
JPH03503292A (en) | 1991-07-25 |
KR900070586A (en) | 1990-08-16 |
EP0409846A1 (en) | 1991-01-30 |
DK188290D0 (en) | 1990-08-07 |
DK188290A (en) | 1990-08-07 |
WO1989008696A1 (en) | 1989-09-21 |
DE3807921A1 (en) | 1989-09-21 |
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