EP0912696B1 - Aqueous bleach and disinfectant - Google Patents

Aqueous bleach and disinfectant Download PDF

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Publication number
EP0912696B1
EP0912696B1 EP97924946A EP97924946A EP0912696B1 EP 0912696 B1 EP0912696 B1 EP 0912696B1 EP 97924946 A EP97924946 A EP 97924946A EP 97924946 A EP97924946 A EP 97924946A EP 0912696 B1 EP0912696 B1 EP 0912696B1
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weight
preparations
contain
alkali metal
carbon atoms
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German (de)
French (fr)
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EP0912696A1 (en
Inventor
Mercedes Mendoza
Maite Canellas
Elisabet Dejorge
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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
    • C11D3/02Inorganic compounds ; Elemental compounds
    • C11D3/04Water-soluble compounds
    • C11D3/044Hydroxides or bases
    • 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
    • C11D10/00Compositions of detergents, not provided for by one single preceding group
    • C11D10/04Compositions of detergents, not provided for by one single preceding group based on mixtures of surface-active non-soap compounds and soap
    • 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
    • C11D3/395Bleaching agents
    • C11D3/3956Liquid compositions
    • 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
    • C11D3/48Medical, disinfecting agents, disinfecting, antibacterial, germicidal or antimicrobial compositions
    • 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
    • C11D1/00Detergent compositions based essentially on surface-active compounds; Use of these compounds as a detergent
    • C11D1/02Anionic compounds
    • C11D1/12Sulfonic acids or sulfuric acid esters; Salts thereof
    • C11D1/29Sulfates of polyoxyalkylene ethers
    • 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
    • C11D1/00Detergent compositions based essentially on surface-active compounds; Use of these compounds as a detergent
    • C11D1/66Non-ionic compounds
    • C11D1/75Amino oxides

Definitions

  • the invention relates to new aqueous bleaching and disinfecting agents containing alkali metal hypochlorites, Alkyl ether sulfates, amine oxides, fatty acid salts and alkali metal hydroxides in selected proportions.
  • EP-A 0 274 885 recommends the use of mixtures of linear and branched amine oxides. According to the teaching of EP-A 0 145 084 (Unilever), mixtures of amine oxides with soaps, sarcosinates, taurides or sugar esters can also be used for this purpose.
  • EP-A 0 137 551 and EP-A 0 447 261 (Unilever) the use of amine oxides with soap or sarcosinate and other anionic surfactants, for example alkyl sulfates, alkyl ether sulfates, secondary alkane sulfonates or alkyl benzene sulfonates as a thickening component, is known.
  • EP-A 0 156 438 reports on the use of alkylarylsulfonates as thickeners in aqueous bleaching agents which contain certain stilbene dyes as optical brighteners.
  • ES-A 8801389 Henkel Ibérica
  • aqueous hypochlorite solutions which predominantly contain alkyl ether sulfates and small amounts of amine oxides as surfactant components.
  • aqueous bleaching agent compositions containing sodium hypochlorite and anionic surfactants are also known.
  • the hypochlorite concentration of these agents is 0.1 to 8 and preferably 0.5 to 5% by weight of active chlorine.
  • Aqueous bleaching and cleaning agents containing alkali metal hypochlorites, Alkyl sulfates, amine oxides, fatty acid and alkali metal hydroxides are known from WO-A-95/08610, WO-A-95/03383 and EP-A-0635568.
  • German patent DE-C1 43 33 100 the applicant has already proposed stable and sufficiently viscous aqueous bleaching and cleaning agents based on hypochlorites, fatty alcohol ether sulfates and amine oxides, which contain amine oxide phosphonic acids as a mandatory component. Even if the preparations are not objectionable from an application point of view, the use of phosphonic acids is not without problems with regard to the introduction of phosphorus compounds into surface waters. Since the amine oxide phosphonic acids are also comparatively expensive ingredients, there continues to be a need on the market for simple, viscous formulations which are characterized by high storage stability, chlorine resistance and good dispersing properties with a low hypochlorite content. The object of the invention was therefore to provide new aqueous bleaching and disinfecting agents which are free from the disadvantages described.
  • Alkali metal hypochlorites are to be understood as meaning lithium, potassium and in particular sodium hypochlorite.
  • the hypochlorites can preferably be used in amounts of 1.5 to 2% by weight, based on the composition become.
  • Alkyl ether sulfates are known anionic surfactants which are obtained by sulfation of nonionic surfactants of the alkyl polyglycol ether type and subsequent neutralization.
  • the alkyl ether sulfates which are suitable for the purposes of the agents according to the invention follow the formula ( I ) R 1 O- (CH 2 CH 2 O) n SO 3 X in which R 1 represents an alkyl radical having 12 to 18 carbon atoms, n represents numbers 2 to 5 and X represents sodium or potassium.
  • Typical examples are the sodium salts of sulfates of the C 12/14 cocoalcohol-2, -2,3- and -3-EO adduct.
  • the alkyl ether sulfates can have a conventional or narrow homolog distribution.
  • the alkyl ether sulfates are preferably used in amounts of 2 to 4% by weight, based on the composition.
  • Amine oxides are also known substances, which are occasionally attributed to the cationic, but usually the nonionic surfactants. They are prepared from tertiary fatty amines, which usually have either one long and two short or two long and one short alkyl radical, and are oxidized in the presence of hydrogen peroxide.
  • the amine oxides which are suitable for the purposes of the invention follow the formula ( II ) in which R 2 represents a linear or branched alkyl radical having 12 to 18 carbon atoms and R 3 and R 4 independently of one another represent R 2 or an optionally hydroxy-substituted alkyl radical having 1 to 4 carbon atoms.
  • Amine oxides of the formula ( II ) are preferably used in which R 2 and R 3 are C 12/14 and C 12/18 cocoalkyl radicals and R4 is a methyl or a hydroxyethyl radical. Also preferred are amine oxides of the formula (II) in which R 2 is a C 12/14 or C 12/18 cocoalkyl radical and R 3 and R 4 are methyl or hydroxyethyl. The amine oxides are preferably used in amounts of 1.5 to 3% by weight, based on the composition.
  • the agents according to the invention may contain fatty acid salts of the formula ( III ) as further constituents, R 5 CO-OX in which R 5 CO represents an acyl radical having 12 to 22 carbon atoms and X represents an alkali metal.
  • R 5 CO represents an acyl radical having 12 to 22 carbon atoms
  • X represents an alkali metal.
  • Typical examples are the sodium and / or potassium salts of lauric acid, myristic acid, palmitic acid, palmoleic acid, stearic acid, isostearic acid, oleic acid, elaidic acid, petroselinic acid, linoleic acid, linolenic acid, elaeostearic acid, arachic acid, gadoleic acid, behenic acid and erucic acid and their mixtures, and their mixtures the pressure splitting of technical fats and oils.
  • Salts of technical coconut or tallow fatty acids are preferably used. Since the formulations according to the invention are strongly alkaline, it is also possible to use the fatty acids instead of the salts, which are neutralized in situ when introduced into the mixture.
  • the fatty acid salts are preferably used in amounts of 1.5 to 2% by weight.
  • Potassium hydroxide and in particular sodium hydroxide come into consideration as alkali metal hydroxides. which are preferably used in amounts of 1.5 to 2 wt .-% and serve the pH to set the mean to an optimal value of 12.5 to 14.
  • the agents according to the invention have a viscosity above 100 mPas - measured at 20 ° C. in a Brookfield viscometer - are stable on storage, resistant to chlorine consumption and stand out with an excellent dispersibility for dye pigments.
  • auxiliaries and additives which the preparations may further contain are further chlorine-stable surfactants or hydrotropes, such as alkyl sulfates, alkyl sulfonates, alkylbenzenesulfonates, Xylene sulfonates, sarcosinates, taurides, isethionates, sulfosuccinates, betaines, sugar esters, Fatty alcohol polyglycol ethers and alkyl oligoglycosides.
  • surfactants or hydrotropes such as alkyl sulfates, alkyl sulfonates, alkylbenzenesulfonates, Xylene sulfonates, sarcosinates, taurides, isethionates, sulfosuccinates, betaines, sugar esters, Fatty alcohol polyglycol ethers and alkyl oligoglycosides.
  • the sum of these makes additional
  • alkyl sulfates in amounts of 0.5 to 3% by weight is particularly preferred.
  • agents active chlorine-stable fragrances, optical brighteners, dyes and pigments in a total of 0.01 to 0.5 wt .-% - based on the agent - included.
  • active chlorine resistant Known fragrances include, for example, monocyclic and bicyclic monoterpene alcohols and their esters with acetic or propionic acid (e.g. isoborneal, dihydroterpene oil, Isobomylacetate, dihydroterpenylacetate).
  • the optical brighteners can be, for example the potash salt of 4,4'-bis (1,2,3-triazolyl) - (2-) - stilbin-2,2-sulfonic acid act under the brand name Phorwite® BHC 766 is sold.
  • the color pigments include green chlorophthalocyanines (Pigmosol® Green, Hostaphine® Green) or yellow Solar Yellow® BG 300 (Sandoz) in question.
  • the agents according to the invention are produced by stirring. If necessary, the obtained Decant or filter product to remove foreign bodies and / or agglomerates.
  • the viscosity was determined at 20 ° C. using a Brookfield viscometer (model RCT, spindle No. 1 or No. 2, 200 rpm). To determine the chlorine stability, the test mixtures were stored in a colorless plastic bottle under the influence of daylight and the active chlorine content was determined.
  • the formulas R1 to R3 are according to the invention, the formulas R4 to R7 are used for comparison. The results are summarized in Table 1 (quantitative data as% by weight)
  • the preparations according to the invention are those which are amine oxidephosphonic acids Stabilizers contain not only equivalent in terms of viscosity, storage stability and chlorine consumption, but z. T. are even superior.

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  • Chemical & Material Sciences (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Engineering & Computer Science (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Oil, Petroleum & Natural Gas (AREA)
  • Wood Science & Technology (AREA)
  • Organic Chemistry (AREA)
  • Inorganic Chemistry (AREA)
  • Detergent Compositions (AREA)
  • Cosmetics (AREA)
  • Agricultural Chemicals And Associated Chemicals (AREA)

Description

Gebiet der ErfindungField of the Invention

Die Erfindung betrifft neue wäßrige Bleich- und Desinfektionsmittel, enthaltend Alkalimetallhypochlorite, Alkylethersulfate, Aminoxide, Fettsäuresalze und Alkalimetallhydroxide in ausgewählten Mengenverhältnissen.The invention relates to new aqueous bleaching and disinfecting agents containing alkali metal hypochlorites, Alkyl ether sulfates, amine oxides, fatty acid salts and alkali metal hydroxides in selected proportions.

Stand der TechnikState of the art

In der Vergangenheit haben sich in den Bereichen Hygiene und Desinfektion solche Bleichmittel auf der Grundlage von Alkalimetallhypochloriten bewährt, die über eine bemerkenswerte Viskosität verfügen und sich daher sowohl für die Behandlung horizontaler als auch geneigter und vor allem vertikaler Oberflächen eignen. Die Viskosität dieser Mittel bewirkt, daß die Kontaktzeit zwischen diesen und den zu behandelnden Oberflächen wesentlich größer ist als bei handelsüblichen Flüssigprodukten, die rasch von der Oberfläche abfließen.In the past, such bleaches have appeared in the areas of hygiene and disinfection proven on the basis of alkali metal hypochlorites, which have a remarkable viscosity and therefore suitable for both horizontal and inclined and above all vertical treatment Surfaces. The viscosity of these agents causes the contact time between them and the surfaces to be treated is much larger than that of commercially available liquid products drain quickly from the surface.

In der Vergangenheit hat es nicht an Versuchen gemangelt, derartig viskose Bleich- und Desinfektionsmittel bereitzustellen. So wurde beispielsweise gefunden, daß bestimmte Tenside oder Tensidgemische eine verdickende Wirkung auf wäßrige Hypochloritlösungen ausüben. In der EP-A 0 274 885 (ICI) wird beispielsweise der Einsatz von Mischungen linearer und verzweigter Aminoxide empfohlen. Gemäß der Lehre der EP-A 0 145 084 (Unilever) können für diesen Zweck auch Mischungen von Aminoxiden mit Seifen, Sarkosinaten, Tauriden oder Zuckerestern eingesetzt werden. Aus den Schriften EP-A 0 137 551 und EP-A 0 447 261 (Unilever) ist der Einsatz von Aminoxiden mit Seife oder Sarkosinat und weiteren anionischen Tensiden, beispielsweise Alkylsulfaten, Alkylethersulfaten, sekundären Alkansulfonaten oder Alkylbenzolsulfonaten als verdickende Komponente bekannt. Über die Verwendung von Alkylarylsulfonaten als Verdickungsmitteln in wäßrigen Bleichmitteln, die bestimmte Stilbenfarbstoffe als optische Aufheller enthalten, wird in der EP-A 0 156 438 berichtet. Gegenstand der ES-A 8801389 (Henkel Ibérica) sind Bleichmittel auf Basis von wäßrigen Hypochloritlösungen, die als Tensidkomponente überwiegend Alkylethersulfate und daneben kleine Anteile an Aminoxiden enthalten. Aus der EP-A1 0 447 261 sind weiterhin wäßrige Bleichmittelzusammensetzungen mit einem Gehalt an Natriumhypochlorit und anionischen Tensiden bekannt. Die Hypochloritkonzentration dieser Mittel liegt jedoch bei 0,1 bis 8 und vorzugsweise 0,5 bis 5 Gew.-% Aktivchlor.There has been no shortage of attempts in the past to provide such viscous bleaching and disinfecting agents. For example, it has been found that certain surfactants or surfactant mixtures have a thickening effect on aqueous hypochlorite solutions. For example, EP-A 0 274 885 (ICI) recommends the use of mixtures of linear and branched amine oxides. According to the teaching of EP-A 0 145 084 (Unilever), mixtures of amine oxides with soaps, sarcosinates, taurides or sugar esters can also be used for this purpose. From the documents EP-A 0 137 551 and EP-A 0 447 261 (Unilever) the use of amine oxides with soap or sarcosinate and other anionic surfactants, for example alkyl sulfates, alkyl ether sulfates, secondary alkane sulfonates or alkyl benzene sulfonates as a thickening component, is known. EP-A 0 156 438 reports on the use of alkylarylsulfonates as thickeners in aqueous bleaching agents which contain certain stilbene dyes as optical brighteners. The subject of ES-A 8801389 (Henkel Ibérica) are bleaching agents based on aqueous hypochlorite solutions, which predominantly contain alkyl ether sulfates and small amounts of amine oxides as surfactant components. From EP-A1 0 447 261 aqueous bleaching agent compositions containing sodium hypochlorite and anionic surfactants are also known. However, the hypochlorite concentration of these agents is 0.1 to 8 and preferably 0.5 to 5% by weight of active chlorine.

Wäßrige Bleich- und Reinigungsmittel enthaltend Alkalimetallhypochlorite, Alkylsulfate, Aminoxide, Fettsäure und Alkalimetallhydroxide sind aus den WO-A-95/08610, WO-A-95/03383 und EP-A-0635568 bekannt.Aqueous bleaching and cleaning agents containing alkali metal hypochlorites, Alkyl sulfates, amine oxides, fatty acid and alkali metal hydroxides are known from WO-A-95/08610, WO-A-95/03383 and EP-A-0635568.

Im Deutschen Patent DE-C1 43 33 100 hat die Anmelderin bereits stabile und ausreichend viskose wäßrige Bleich- und Reinigungsmittel auf Basis von Hypochloriten, Fettalkoholethersulfaten und Aminoxiden vorgeschlagen, die als zwingende Komponente Aminoxidphosphonsäuren enthalten. Auch wenn die Zubereitungen aus anwendungstechnischer Sicht nicht zu beanstanden sind, ist die Mitverwendung von Phosphonsäuren im Hinblick auf den Eintrag von Phosphorverbindungen in Oberflächengewässer nicht ohne Probleme. Nachdem es sich bei den Aminoxidphosphonsäuren zudem um vergleichsweise kostspielige Inhaltsstoffe handelt, besteht im Markt auch weiterhin ein Bedürfnis nach möglichst einfachen, viskosen Formulierungen, die sich bei niedrigem Hypochloritgehalt durch eine hohe Lagerstabilität, Chlorbeständigkeit und gute Dispergiereigenschaften auszeichnen.
Die Aufgabe der Erfindung hat somit darin bestanden, neue wäßrige Bleich- und Desinfektionsmittel zur Verfügung zu stellen, die frei von den geschilderten Nachteilen sind.
In German patent DE-C1 43 33 100 , the applicant has already proposed stable and sufficiently viscous aqueous bleaching and cleaning agents based on hypochlorites, fatty alcohol ether sulfates and amine oxides, which contain amine oxide phosphonic acids as a mandatory component. Even if the preparations are not objectionable from an application point of view, the use of phosphonic acids is not without problems with regard to the introduction of phosphorus compounds into surface waters. Since the amine oxide phosphonic acids are also comparatively expensive ingredients, there continues to be a need on the market for simple, viscous formulations which are characterized by high storage stability, chlorine resistance and good dispersing properties with a low hypochlorite content.
The object of the invention was therefore to provide new aqueous bleaching and disinfecting agents which are free from the disadvantages described.

Beschreibung der ErfindungDescription of the invention

Gegenstand der Erfindung sind wäßrige Bleich- und Desinfektionsmittel mit einer Viskosität oberhalb von 100 mPas - gemessen bei 20°C in einem Brookfield-Viskosimeter - und frei von Aminoxidphos-phonsäuren, enthaltend - bezogen auf die Mittel -

  • (a) 1 bis 3 Gew.-% Alkalimetallhypochlorite,
  • (b) 1 bis 5 Gew.-% Alkylethersulfate der Formel (I), R1O-(CH2CH2O)nSO3X in der R1 für einen Alkylrest mit 12 bis 18 Kohlenstoffatomen, n für Zahlen 2 bis 5 und X für Natrium oder Kalium steht,
  • (c) 1 bis 4 Gew.-% Aminoxide,
  • (d) 1 bis 4 Gew.-% Fettsäuresalze und
  • (e) 0,1 bis 2 Gew.-% Alkalimetallhydroxide
  • sowie gegebenenfalls weitere übliche Hilfs- und Zusatzstoffe. The invention relates to aqueous bleaching and disinfecting agents with a viscosity above 100 mPas - measured at 20 ° C. in a Brookfield viscometer - and free of amine oxide phosphonic acids, containing - based on the agents -
  • (a) 1 to 3% by weight of alkali metal hypochlorites,
  • (b) 1 to 5% by weight of alkyl ether sulfates of the formula (I), R 1 O- (CH 2 CH 2 O) n SO 3 X in which R 1 represents an alkyl radical having 12 to 18 carbon atoms, n represents numbers 2 to 5 and X represents sodium or potassium,
  • (c) 1 to 4% by weight of amine oxides,
  • (d) 1 to 4% by weight of fatty acid salts and
  • (e) 0.1 to 2 wt% alkali metal hydroxides
  • and, if appropriate, other customary auxiliaries and additives.

    Überraschenderweise wurde gefunden, daß sich Bleich- und Desinfektionsmittel der angegebenen Zusammensetzung mit dem gewünschten Anforderungsprofil auch ohne Mitverwendung von Aminoxidphosphonsäuren zur Verfügung stellen lassen, wenn man die genannten Inhaltsstoffe in den angegebenen Mengen abmischt.Surprisingly, it was found that bleaching agents and disinfectants of the stated composition with the desired requirement profile even without the use of amine oxide phosphonic acids can be made available if one of the ingredients mentioned in the specified Mixes quantities.

    Alkalimetallhypochloritealkali metal hypochlorites

    Unter Alkalimetallhypochloriten sind Lithium-, Kalium- und insbesondere Natriumhypochlorit zu verstehen. Die Hypochlorite können vorzugsweise in Mengen von 1,5 bis 2 Gew.-% - bezogen auf die Mittel-eingesetzt werden.Alkali metal hypochlorites are to be understood as meaning lithium, potassium and in particular sodium hypochlorite. The hypochlorites can preferably be used in amounts of 1.5 to 2% by weight, based on the composition become.

    Alkylethersulfatealkyl ether

    Alkylethersulfate stellen bekannte anionische Tenside dar, die durch Sulfatierung von nichtionischen Tensiden vom Typ der Alkylpolyglycolether und nachfolgende Neutralisation erhalten werden. Die im Sinne der erfindungsgemäßen Mittel in Betracht kommenden Alkylethersulfate folgen der Formel (I), R1O-(CH2CH2O)nSO3X in der R1 für einen Alkylrest mit 12 bis 18 Kohlenstoffatomen, n für Zahlen 2 bis 5 und X für Natrium oder Kalium steht. Typische Beispiele sind die Natriumsalze von Sulfaten des C12/14-Kokosalkohol-2,-2,3- und -3-EO-Adduktes. Die Alkylethersulfate können eine konventionelle oder eingeengte Homologenverteilung aufweisen. Vorzugsweise werden die Alkylethersulfate in Mengen von 2 bis 4 Gew.-%-bezogen auf die Mittel - eingesetzt.Alkyl ether sulfates are known anionic surfactants which are obtained by sulfation of nonionic surfactants of the alkyl polyglycol ether type and subsequent neutralization. The alkyl ether sulfates which are suitable for the purposes of the agents according to the invention follow the formula ( I ) R 1 O- (CH 2 CH 2 O) n SO 3 X in which R 1 represents an alkyl radical having 12 to 18 carbon atoms, n represents numbers 2 to 5 and X represents sodium or potassium. Typical examples are the sodium salts of sulfates of the C 12/14 cocoalcohol-2, -2,3- and -3-EO adduct. The alkyl ether sulfates can have a conventional or narrow homolog distribution. The alkyl ether sulfates are preferably used in amounts of 2 to 4% by weight, based on the composition.

    Aminoxideamine oxides

    Auch Aminoxide stellen bekannte Stoffe dar, die gelegentlich den kationischen, in der Regel jedoch den nichtionischen Tensiden zugerechnet werden. Zu ihrer Herstellung geht man von tertiären Fettaminen aus, die üblicherweise entweder einen langen und zwei kurze oder zwei lange und einen kurzen Alkylrest aufweisen, und oxidiert sie in Gegenwart von Wasserstoffperoxid. Die im Sinne der Erfindung in Betracht kommenden Aminoxide folgen der Formel (II),

    Figure 00040001
    in der R2 für einen linearen oder verzweigten Alkylrest mit 12 bis 18 Kohlenstoffatomen sowie R3 und R4 unabhängig voneinander für R2 oder einen gegebenenfalls hydroxysubstituierten Alkylrest mit 1 bis 4 Kohlenstoffatomen stehen. Vorzugsweise werden Aminoxide der Formel (II) eingesetzt, in der R2 und R3 für C12/14- bzw. C12/18-Kokosalkylreste stehen und R4 einen Methyl- oder einen Hydroxyethylrest bedeutet. Ebenfalls bevorzugt sind Aminoxide der Formel (II), in denen R2 für einen C12/14- bzw. C12/18-Kokosalkylrest steht und R3 und R4 die Bedeutung eines Methyl- oder Hydroxyethylrestes haben. Vorzugsweise werden die Aminoxide in Mengen von 1,5 bis 3 Gew.-% - bezogen auf die Mittel - eingesetzt.Amine oxides are also known substances, which are occasionally attributed to the cationic, but usually the nonionic surfactants. They are prepared from tertiary fatty amines, which usually have either one long and two short or two long and one short alkyl radical, and are oxidized in the presence of hydrogen peroxide. The amine oxides which are suitable for the purposes of the invention follow the formula ( II )
    Figure 00040001
    in which R 2 represents a linear or branched alkyl radical having 12 to 18 carbon atoms and R 3 and R 4 independently of one another represent R 2 or an optionally hydroxy-substituted alkyl radical having 1 to 4 carbon atoms. Amine oxides of the formula ( II ) are preferably used in which R 2 and R 3 are C 12/14 and C 12/18 cocoalkyl radicals and R4 is a methyl or a hydroxyethyl radical. Also preferred are amine oxides of the formula (II) in which R 2 is a C 12/14 or C 12/18 cocoalkyl radical and R 3 and R 4 are methyl or hydroxyethyl. The amine oxides are preferably used in amounts of 1.5 to 3% by weight, based on the composition.

    Fettsäuresalzefatty acid salts

    Als weitere Bestandteile können die erfindungsgemäßen Mittel Fettsäuresalze der Formel (III) enthalten, R5CO-OX in der R5CO für einen Acylrest mit 12 bis 22 Kohlenstoffatomen und X für ein Alkalimetall steht. Typische Beispiele sind die Natrium- und/oder Kaliumsalze der Laurinsäure, Myristinsäure, Palmitinsäure, Palmoleinsäure, Stearinsäure, Isostearinsäure, Ölsäure, Elaidinsäure, Petroselinsäure, Linolsäure, Linolensäure, Elaeostearinsäure, Arachinsäure, Gadoleinsäure, Behensäure und Erucasäure sowie deren technische Mischungen, wie sie bei der Druckspaltung technischer Fette und Öle anfallen. Vorzugsweise werden Salze technischer Kokos- oder Talgfettsäuren eingesetzt. Da die erfindungsgemäßen Rezepturen stark alkalisch eingestellt sind, können anstelle der Salze auch die Fettsäuren eingesetzt werden, die beim Eintragen in die Mischung in situ neutralisiert werden. Vorzugsweise werden die Fettsäuresalze in Mengen von 1,5 bis 2 Gew.-% eingesetzt. The agents according to the invention may contain fatty acid salts of the formula ( III ) as further constituents, R 5 CO-OX in which R 5 CO represents an acyl radical having 12 to 22 carbon atoms and X represents an alkali metal. Typical examples are the sodium and / or potassium salts of lauric acid, myristic acid, palmitic acid, palmoleic acid, stearic acid, isostearic acid, oleic acid, elaidic acid, petroselinic acid, linoleic acid, linolenic acid, elaeostearic acid, arachic acid, gadoleic acid, behenic acid and erucic acid and their mixtures, and their mixtures the pressure splitting of technical fats and oils. Salts of technical coconut or tallow fatty acids are preferably used. Since the formulations according to the invention are strongly alkaline, it is also possible to use the fatty acids instead of the salts, which are neutralized in situ when introduced into the mixture. The fatty acid salts are preferably used in amounts of 1.5 to 2% by weight.

    Alkalimetallhydroxidealkali metal hydroxides

    Als Alkalimetallhydroxide kommen Kaliumhydroxid und insbesondere Natriumhydroxid in Betracht, welche vorzugsweise in Mengen von 1,5 bis 2 Gew.-% eingesetzt werden und dazu dienen, den pH-Wert der Mittel auf einen optimalen Wert von 12,5 bis 14 einzustellen.Potassium hydroxide and in particular sodium hydroxide come into consideration as alkali metal hydroxides. which are preferably used in amounts of 1.5 to 2 wt .-% and serve the pH to set the mean to an optimal value of 12.5 to 14.

    Gewerbliche AnwendbarkeitIndustrial applicability

    Die erfindungsgemäßen Mittel weisen eine Viskosität oberhalb von 100 mPas - gemessen bei 20°C in einem Brookfield-Viskosimeter - auf, sind lagerstabil, gegen Chlorzehrung beständig und zeichnen sich durch ein ausgezeichnetes Dispergiervermögen für Farbstoffpigmente aus.The agents according to the invention have a viscosity above 100 mPas - measured at 20 ° C. in a Brookfield viscometer - are stable on storage, resistant to chlorine consumption and stand out with an excellent dispersibility for dye pigments.

    Als Hilfs- und Zusatzstoffe, die die Zubereitungen weiterhin enthalten können, kommen beispielsweise weitere chlorstabile Tenside bzw. Hydrotrope in Betracht, wie etwa Alkylsulfate, Alkylsulfonate, Alkylbenzolsulfonate, Xylolsulfonate, Sarkosinate, Tauride, Isethionate, Sulfosuccinate, Betaine, Zuckerester, Fettalkoholpolyglycolether und Alkyloligoglykoside. Vorzugsweise macht die Summe dieser zusätzlichen Tenside höchstens 10 Gew.-% der Gesamtmenge an Tensiden in der Rezeptur aus. Die Mitverwendung von Alkylsulfaten in Mengen von 0,5 bis 3 Gew.-% ist dabei besonders bevorzugt. Darüberhinaus können die Mittel aktivchlorstabile Duftstoffe, optische Aufheller, Farbstoffe und Pigmente in Mengen von insgesamt 0,01 bis 0,5 Gew.-% - bezogen auf die Mittel - enthalten. Zu den als aktivchlorbeständig bekannten Duftstoffen zählen beispielsweise monocyclische und bicyclische Monoterpenalkohole sowie deren Ester mit Essig- oder Propionsäure (z.B. Isoborneal, Dihydroterpenöl, Isobomylacetat, Dihydroterpenylacetat). Bei den optischen Aufhellern kann es sich beispielsweise um das Kalisalz der 4,4'-bis-(1,2,3-Triazolyl)-(2-)-Stilbin-2,2-sulfonsäure handeln, das unter der Marke Phorwite® BHC 766 vertrieben wird. Als Farbpigmente kommen u.a. grüne Chlorophthalocyanine (Pigmosol® Green, Hostaphine® Green) oder gelbes Solar Yellow® BG 300 (Sandoz) in Frage. Die Herstellung der erfindungsgemäßen Mittel erfolgt mittels Umrühren. Gegebenenfalls kann das erhaltene Produkt zur Abtrennung von Fremdkörpern und/oder Agglomeraten dekantiert oder filtriert werden. Examples of auxiliaries and additives which the preparations may further contain are further chlorine-stable surfactants or hydrotropes, such as alkyl sulfates, alkyl sulfonates, alkylbenzenesulfonates, Xylene sulfonates, sarcosinates, taurides, isethionates, sulfosuccinates, betaines, sugar esters, Fatty alcohol polyglycol ethers and alkyl oligoglycosides. Preferably the sum of these makes additional ones Surfactants at most 10 wt .-% of the total amount of surfactants in the recipe. The shared use of alkyl sulfates in amounts of 0.5 to 3% by weight is particularly preferred. Furthermore can the agents active chlorine-stable fragrances, optical brighteners, dyes and pigments in a total of 0.01 to 0.5 wt .-% - based on the agent - included. To those as active chlorine resistant Known fragrances include, for example, monocyclic and bicyclic monoterpene alcohols and their esters with acetic or propionic acid (e.g. isoborneal, dihydroterpene oil, Isobomylacetate, dihydroterpenylacetate). The optical brighteners can be, for example the potash salt of 4,4'-bis (1,2,3-triazolyl) - (2-) - stilbin-2,2-sulfonic acid act under the brand name Phorwite® BHC 766 is sold. The color pigments include green chlorophthalocyanines (Pigmosol® Green, Hostaphine® Green) or yellow Solar Yellow® BG 300 (Sandoz) in question. The The agents according to the invention are produced by stirring. If necessary, the obtained Decant or filter product to remove foreign bodies and / or agglomerates.

    BeispieleExamples

    Die Viskosität wurde bei 20°C mit Hilfe eines Brookfield-Viskosimeters (Modell RCT, Spindel Nr.1 oder Nr.2, 200 Upm) bestimmt. Zur Bestimmung der Chlorstabilität wurden die Testmischungen unter dem Einfluß von Tageslicht in einer farblosen Kunststoffflasche gelagert und der Aktivchlorgehalt bestimmt. Die Rezepturen R1 bis R3 sind erfindungsgemäß, die Rezepturen R4 bis R7 dienen zum Vergleich. Die Ergebnisse sind in Tabelle 1 zusammengefaßt (Mengenangaben als Gew.-%)

    Figure 00060001
    The viscosity was determined at 20 ° C. using a Brookfield viscometer (model RCT, spindle No. 1 or No. 2, 200 rpm). To determine the chlorine stability, the test mixtures were stored in a colorless plastic bottle under the influence of daylight and the active chlorine content was determined. The formulas R1 to R3 are according to the invention, the formulas R4 to R7 are used for comparison. The results are summarized in Table 1 (quantitative data as% by weight)
    Figure 00060001

    Man erkennt, daß die erfindungsgemäßen Zubereitungen denen, die Aminoxidphosphonsäuren als Stabilisatoren enthalten, im Hinblick auf Viskosität, Lagerstabilität und Chlorzehrung nicht nur gleichwertig, sondern z. T. sogar überlegen sind.It can be seen that the preparations according to the invention are those which are amine oxidephosphonic acids Stabilizers contain not only equivalent in terms of viscosity, storage stability and chlorine consumption, but z. T. are even superior.

    Claims (5)

    1. Water-based bleaching and disinfecting preparations which have a viscosity above 100 mPas, as measured at 20°C in a Brookfield viscosimeter, and which are free from amine oxide phosphonic acids, characterized in that they contain - based on the preparation -
      (a) 1 to 3% by weight of alkali metal hypochlorites,
      (b) 1 to 5% by weight of C12-18 alkyl ether sulfates corresponding to formula (I): R1O-(CH2CH2O)nSO3X in which R1 is an alkyl group containing 12 to 18 carbon atoms, n is a number of 2 to 5 and X stands for sodium or potassium.,
      (c) 1 to 4% by weight of amine oxides,
      (d) 1 to 4% by weight of fatty acid salts and
      (e) 0.1 to 2% by weight of alkali metal hydroxides
      and, optionally, other typical auxiliaries and additives.
    2. Preparations as claimed in claim 1, characterized in that they contain sodium hypochlorite.
    3. Preparations as claimed in claim 1 or 2, characterized in that they contain amine oxides corresponding to formula (II):
      Figure 00090001
      in which R2 is a linear or branched alkyl group containing 12 to 18 carbon atoms and R3 and R4 independently of one another have the same meaning as R2 or represent an optionally hydroxysubstituted alkyl group containing 1 to 4 carbon atoms.
    4. Preparations as claimed in claims 1 to 3, characterized in that they contain fatty acid salts corresponding to formula (III): R5CO-OX in which R5CO represents an acyl group containing 12 to 22 carbon atoms and X stands for an alkali metal.
    5. Preparations as claimed in claims 1 to 4, characterized in that they contain sodium hydroxide.
    EP97924946A 1996-05-24 1997-05-14 Aqueous bleach and disinfectant Expired - Lifetime EP0912696B1 (en)

    Applications Claiming Priority (3)

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    DE1996121048 DE19621048C2 (en) 1996-05-24 1996-05-24 Aqueous bleach and disinfectant
    DE19621048 1996-05-24
    PCT/EP1997/002459 WO1997045520A1 (en) 1996-05-24 1997-05-14 Aqueous bleach and disinfectant

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    EP0912696B1 true EP0912696B1 (en) 2003-04-09

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    DE59912187D1 (en) * 1998-05-08 2005-07-21 Henkel Kgaa BLEACHING AND DISINFECTANT
    DE19902904A1 (en) * 1999-01-26 2000-08-03 Henkel Kgaa Bleach and disinfectant
    DE102005041436A1 (en) * 2005-08-31 2007-03-01 Henkel Kgaa Aqueous bleaching composition, useful to bleach textiles, comprises hypohalogenated bleaching agent, surfactant mixture comprising ether sulfate, alkane sulfonate and amine oxide, foam regulator, and optional alkali silicate and stabilizers

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    US4474677A (en) * 1981-11-06 1984-10-02 Lever Brothers Company Colored aqueous alkalimetal hypochlorite compositions
    GB8325541D0 (en) * 1983-09-23 1983-10-26 Unilever Plc Liquid thickened bleaching composition
    GB8332271D0 (en) * 1983-12-02 1984-01-11 Unilever Plc Bleaching composition
    EP0635568A1 (en) * 1993-07-23 1995-01-25 The Procter & Gamble Company Thickened hypochlorite detergent compositions with improved cleaning performance
    CN1057790C (en) * 1993-07-23 2000-10-25 普罗格特-甘布尔公司 Thickened aqueous detergent compositions with improved cleaning performance with short chain surfactants
    GB9315760D0 (en) * 1993-07-30 1993-09-15 Nat Starch Chem Corp Bleach compositions
    AU7723494A (en) * 1993-09-20 1995-04-10 Procter & Gamble Company, The Use of hypochlorite-comprising compositions with a short chain surfactant for odour reduction
    DE4333100C1 (en) * 1993-09-29 1994-10-06 Henkel Kgaa Bleaching and disinfecting compositions

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    EP0912696A1 (en) 1999-05-06

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