EP1957621B1 - Stability improvement of liquid hypochlorite-containing washing and cleaning compositions - Google Patents

Stability improvement of liquid hypochlorite-containing washing and cleaning compositions Download PDF

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EP1957621B1
EP1957621B1 EP06818842A EP06818842A EP1957621B1 EP 1957621 B1 EP1957621 B1 EP 1957621B1 EP 06818842 A EP06818842 A EP 06818842A EP 06818842 A EP06818842 A EP 06818842A EP 1957621 B1 EP1957621 B1 EP 1957621B1
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group
use according
hypochlorite
alkali
composition contains
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EP1957621A1 (en
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Carolina Perez
Carlos Malet
Miguel Osset
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Henkel AG and Co KGaA
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Henkel AG and Co KGaA
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    • 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
    • C11D3/395Bleaching agents
    • C11D3/3951Bleaching agents combined with specific additives
    • 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
    • C11D3/40Dyes ; Pigments

Definitions

  • the agents contain more than 0 wt .-% to 0.01 wt .-%, in particular up to 0.005 wt .-% of colored, especially blue and / or green, metal pigment.
  • colored, especially blue and / or green, metal pigment especially blue and / or green, metal pigment.
  • complex compounds of nickel, cobalt, cuprous, iron and / or manganese are preferred; particularly preferred are copper phthalocyanine dyes.
  • the preparations stabilized according to the invention may contain small amounts of one or more bleach-stable fragrances.
  • the optional perfume component is preferably of higher relative volatility than the ingredients optionally responsible for a bleaching odor.

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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)
  • Detergent Compositions (AREA)

Abstract

The improvement of shelf stability in hypochlorite-containing aqueous liquid washing and/or cleaning agents that contain colored metal pigment is achieved by the use of an alkali iodide and a sterically hindered amine.

Description

Die vorliegende Erfindung betrifft die Stabilisierung hypochlorit-haltiger flĆ¼ssiger Waschmittel und/oder Reinigungsmittel fĆ¼r harte OberflƤchen in Haushalten, zum Beispiel zur Reinigung von Kacheln.The present invention relates to the stabilization of hypochlorite-containing liquid detergents and / or cleaners for hard surfaces in households, for example for cleaning tiles.

Natriumhypochlorit ist bekannt als hoch effektives Bleichmittel und wird seit langem, gegebenenfalls zusammen mit Seifen und/oder synthetischen Tensiden, zur Entfernung von Flecken und allen Arten von Anschmutzungen bei der WƤsche von Textilien wie auch beim Reinigen harter OberflƤchen benutzt. Es wird normalerweise in Konzentrationen von etwa 2 bis 10 Gew.-% in Wasser fĆ¼r die Verwendung in Haushalten vertrieben. FĆ¼r solche Zubereitungen ist es nicht unĆ¼blich, dass sie zur Regulierung ihrer ViskositƤt Hydrotrope enthalten.Sodium hypochlorite is known to be a highly effective bleaching agent and has been used for a long time, optionally with soaps and / or synthetic surfactants, to remove stains and all sorts of soils from laundry to textiles as well as hard surface cleaning. It is normally sold in concentrations of about 2 to 10% by weight in water for household use. For such preparations, it is not uncommon for them to contain hydrotropes to regulate their viscosity.

FlĆ¼ssige Waschmittelzubereitungen oder entsprechende Zubereitungen von Reinigungsmitteln fĆ¼r harte OberflƤchen, die Hypochlorit als Bleichkomponente enthalten, sind bei lƤnger andauernder Lagerung anfƤllig gegen einen Verlust an AktivitƤt, insbesondere wegen des dann stattfindenden Abbaus des Hypochlorits. Zu den Inhaltstoffen, die unter Anwendungsgesichtspunkten oder aus Ƥsthetischen GrĆ¼nden in Wasch- und Reinigungsmitteln erwĆ¼nscht sind, gehƶren neben den die Leistung solcher Mittel entscheidend beeinflussenden Wirkstoffen, hier insbesondere das Hypochlorit, auch FƤrbemittel, welche insbesondere flĆ¼ssigen Zubereitungen eine angenehme optische Erscheinungsform geben sollen. Besonders Farbstoffe werden von Hypochlorit in aller Regel leicht oxidativ angegriffen, so dass sich der Farbeindruck hypochlorithaltiger flĆ¼ssiger Mittel bei Lagerung rasch verƤndert.Liquid detergent formulations or corresponding preparations of hard surface cleaners containing hypochlorite as a bleach component are susceptible to loss of activity upon prolonged storage, especially because of the then-degradation of the hypochlorite. Among the ingredients that are desirable from an application point of view or for aesthetic reasons in detergents and cleaners include, in addition to the performance of such agents crucial influencing agents, in particular hypochlorite, and colorants, which should give a pleasant visual appearance in particular liquid preparations. In particular, dyes are attacked by hypochlorite usually slightly oxidative, so that the color impression of hypochlorite-containing liquid agent changes rapidly on storage.

Obwohl es einige VorschlƤge zur Stabilisierung von Alkalihypochlorit in wƤƟrigen Systemen gibt, sind dennoch alternative Lƶsungswege erstrebenswert.Although there are some proposals for stabilizing alkali hypochlorite in aqueous systems, alternative approaches are still desirable.

Die EuropƤische Patentanmeldung EP 0 903 403 schlƤgt zum Beispiel vor, ein Alkyl-(alkoxy)n-sulfat (mit n=0,5 bis 20), welches nur geringe Anteile an unsulfatiertem Material und sehr geringe Anteile an Metallverunreinigungen enthalten darf, zur Erhƶhung der chemischen StabilitƤt flĆ¼ssiger Bleichmittel, die ein Hypohalogenit enthalten, zu verwenden.The European patent application EP 0 903 403 suggests, for example, an alkyl (alkoxy) n -sulfate (where n = 0.5 to 20), which may contain only small amounts of unsulfated material and very low levels of metal impurities, to increase the chemical stability of liquid bleaches a hypohalite containing.

EP-A1-79102 offenbart wƤsserige Hypochloritlƶsungen, enthaltend ein halogeniertes Metallophthalocyaninpigment. EP-A1-79102 discloses aqueous hypochlorite solutions containing a halogenated metallophthalocyanine pigment.

EP-A1-565788 beschreibt die Stabilisierung von wƤsserigen Hypochloritlƶsungen durch Jodat. EP-A1-565788 describes the stabilization of aqueous hypochlorite solutions by iodate.

Schliesslich offenbart EP-A2-1391501 ein Verfahren zur Stabilisierung der ViskositƤt und/oder des Aktivchlorgehalts von flĆ¼ssigen Zusammensetzungen, enthaltend Hypochlorit durch Zugabe bestimmter sterisch gehinderter Amine.Finally disclosed EP-A2-1391501 a method for stabilizing the viscosity and / or the active chlorine content of liquid compositions containing hypochlorite by adding certain hindered amines.

Ɯberraschenderweise wurde nun gefunden, dass bestimmte sterisch gehinderte Amine einen ausgeprƤgten Stabilisierungseffekt sowohl auf Hypochlorit in wƤƟrigen flĆ¼ssigen Wasch- und Reinigungsmitteln haben, wie auch auf Farbpigmente, die in solchen Mitteln normalerweise durch das Hypochlorit rasch abgebaut werden. Als weiterer Vorteil wurde beobachtet, dass ein synergistischer Effekt zwischen solchen sterisch gehinderten Aminen und Alkalijodiden dazu fĆ¼hrt, dass man grĆ¶ĆŸere Mengen an Farbstoffen in hypochlorithaltige Mittel einarbeiten kann als dass dies sonst mƶglich wƤre.Surprisingly, it has now been found that certain sterically hindered amines have a marked stabilizing effect both on hypochlorite in aqueous liquid detergents and cleaners, as well as on color pigments which are normally rapidly degraded in such agents by the hypochlorite. As a further advantage, it has been observed that a synergistic effect between such sterically hindered amines and alkali iodides results in incorporating larger amounts of dyes into hypochlorite-containing agents than would otherwise be possible.

Ein Gegenstand der Erfindung ist daher die gemeinsame Verwendung eines Alkalijodids und eines sterisch gehinderten Amins, welches die Gruppe der allgemeinen Formel (I) aufweist,

Figure imgb0001
in der die Reste R1, R2, R3 und R4 unabhƤngig voneinander fĆ¼r Wasserstoff, eine Methylgruppe oder eine Ethylgrupe stehen mit der MaƟgabe, dass nicht mehr als 2 von diesen Resten gleichzeitig Wasserstoff sind, und X fĆ¼r Wasserstoff, Sauerstoff, eine Methylgruppe, eine Ethylgrupe, -OH oder -OR5 steht, wobei R5 eine C1-4 Alkylgruppe oder eine Cyclohexylgruppe ist, zur Stabilisierung von Hypochlorit-enthaltenden wƤƟrigen flĆ¼ssigen Zusammensetzungen, die farbiges Metallpigment enthalten.An object of the invention is therefore the joint use of an alkali metal iodide and a sterically hindered amine which has the group of the general formula (I),
Figure imgb0001
in which the radicals R 1 , R 2 , R 3 and R 4 independently of one another are hydrogen, a methyl group or an ethyl group, with the proviso that not more than 2 of these radicals are simultaneously hydrogen, and X is hydrogen, oxygen, a Methyl group, an ethyl group, -OH or -OR 5 , wherein R 5 is a C 1-4 alkyl group or a cyclohexyl group, for stabilizing hypochlorite-containing aqueous liquid compositions containing colored metallic pigment.

Ein zweiter Gegenstand der Erfindung ist ein wƤƟriges flĆ¼ssiges Bleichmittel, enthaltend Alkalihypochlorit und farbiges Metallpigment, was dadurch gekennzeichnet ist, dass es zusƤtzlich eine Kombination aus Akalijodid und sterisch gehindertem Amin, welches die Gruppe der allgemeinen Formel (I) aufweist,

Figure imgb0002
in der die Reste R1, R2, R3 und R4 unabhƤngig voneinander fĆ¼r Wasserstoff, eine Methylgruppe oder eine Ethylgrupe stehen mit der MaƟgabe, dass nicht mehr als 2 von diesen Resten gleichzeitig Wasserstoff sind, und X fĆ¼r Wasserstoff, Sauerstoff, eine Methylgruppe, eine Ethylgrupe, -OH oder -OR5 steht, wobei R5 eine C1-4 Alkylgruppe oder eine Cyclohexylgruppe ist, enthƤlt.A second aspect of the invention is an aqueous liquid bleach containing alkali hypochlorite and colored metal pigment characterized by additionally comprising a combination of akaliyodide and hindered amine having the group of general formula (I),
Figure imgb0002
in which the radicals R 1 , R 2 , R 3 and R 4 independently of one another are hydrogen, a methyl group or an ethyl group, with the proviso that not more than 2 of these radicals are simultaneously hydrogen, and X is hydrogen, oxygen, a methyl group, an ethyl group, -OH or -OR 5, where R 5 is a C 1-4 alkyl group or a cyclohexyl group, contains.

Unter den erfindungsgemƤƟ bevorzugten Aminen sind solche, bei denen die Gruppe der allgemeinen Formel (I) Teil eines Piperidinringes ist. In diesen weist der Piperidinring zusƤtzlich zu den Substituenten R1, R2, R3, R4 und X vorzugsweise einen Substituenten in Position 4 auf, der -OH, -NHR6 oder Ć¼ber eine Doppelbindung verknĆ¼pfter Sauerstoff ist, wobei R6 eine C1-4 Alkylgruppe oder eine Cyclohexylgruppe ist.Among the inventively preferred amines are those in which the group of general formula (I) is part of a piperidine ring. In these, in addition to the substituents R 1 , R 2 , R 3 , R 4 and X, the piperidine ring preferably has a substituent in position 4 which is -OH, -NHR 6 or oxygen linked via a double bond, where R 6 is a C 1-4 alkyl group or a cyclohexyl group.

Normalerweise ist es ausreichend, wenn mehr als 0 Gew.-% bis hin zu etwa 0,1 Gew.-%, insbesondere etwa 0,0005 Gew.-% bis hin zu nicht mehr als etwa 0,03 Gew.-% an dem sterisch gehinderten Amin in dem zu stabilisierenden flĆ¼ssigen Mittel enthalten ist.Normally, it is sufficient if more than 0 wt.% Up to about 0.1 wt.%, In particular about 0.0005 wt.% Up to not more than about 0.03 wt sterically hindered amine is included in the liquid agent to be stabilized.

In einer bevorzugten AusfĆ¼hrungsform enthƤlt das gemƤƟ der Erfindung stabilisierte flĆ¼ssige Mittel 0,5 Gew.-% bis 5 Gew.-% Alkalihypochlorit, insbesondere Natriumhypochlorit.In a preferred embodiment, the liquid agent stabilized according to the invention contains from 0.5% to 5% by weight alkali hypochlorite, especially sodium hypochlorite.

Derartige Zubereitungen sind insbesondere geeignet und sehr effektiv als Reinigungsmittel fĆ¼r harte OberflƤchen, zum Beispiel zur Verwendung an WƤnden, ArbeitsflƤchen, FuƟbƶden und Ƥhnlichem. Die Mittel sind, im wesentlichen wegen ihres Gehaltes an Hypochlorit, besonders geeignet zur Entfernung von Anschmutzungen, wie sie in KĆ¼chen oder Badezimmern auftreten, einschlieƟlich der schmierigen Anschmutzungen, die nach der Benutzung von Badewannen, Duschkabinen und Waschbecken auftreten kƶnnen.Such formulations are particularly suitable and very effective as hard surface cleaners, for example for use on walls, work surfaces, floors and the like. The agents, especially because of their hypochlorite content, are particularly suitable for removing stains such as occur in kitchens or bathrooms, including greasy stains that may occur after using bathtubs, shower cubicles and sinks.

Ein Bleichmittel in Form von Hypochlorit ist ein wesentlicher Bestandteil der erfindungsgemƤƟen Mittel. Bleichmittel an sich sind durchaus bekannte Komponenten von Reinigungsmittelzusammensetzungen und sind insbesondere erfolgreich im BekƤmpfen von Mehltau und Schimmel, Anschmutzungen, die sich in Seifenablagerungen oder in Gemeinschaft mit diesen hƤufig antreffen lassen. Obzwar auch andere Alkalihypochlorite, wie beispielsweise Kaliumhypochlorit, brauchbar sind, ist es doch bevorzugt, in erfindungsgemƤƟ stabilisierten Mitteln Natriumhypochlorit einzusetzen. In handelsĆ¼blichen wƤƟrigen Natriumhypochlorit-Lƶsungen sind oft betrƤchtliche Mengen an Chlorid-Salzen enthalten. Diese kƶnnen ohne weiteres zur Herstellung erfindungsgemƤƟer Mittel verwendet werden, so dass man auf den Einsatz von hochreinem NaOCl nicht notwendigerweise angewiesen ist. In einer bevorzugten AusfĆ¼hrungsform der Erfindung enthalten die Mittel 0,5 Gew.-% bis 4,5 Gew.-%, insbesondere 1 Gew.-% bis 4 Gew.-% Alkalihypochlorit.A bleaching agent in the form of hypochlorite is an essential component of the compositions according to the invention. Bleaches per se are well-known components of detergent compositions and are particularly successful in controlling mildew and mildew, soils that are commonly found in soap deposits or in association with them. Although other alkali metal hypochlorites, such as potassium hypochlorite, are useful, it is still preferred to use sodium hypochlorite in stabilized compositions of this invention. Commercially available aqueous sodium hypochlorite solutions often contain considerable amounts of chloride salts. These can readily be used for the production of agents according to the invention, so that it is not necessarily dependent on the use of high-purity NaOCl. In a preferred embodiment of the invention, the compositions contain 0.5% by weight to 4.5% by weight, in particular 1% by weight to 4% by weight, of alkali metal hypochlorite.

Vorzugsweise enthalten die Mittel mehr als 0 Gew.-% bis 0,01 Gew.-%, insbesondere bis zu 0,005 Gew.-% an farbigem, insbesondere blauem und/oder grĆ¼nem, Metallpigment. Unter diesen sind Komplexverbindungen des Nickels, Cobalts, Cupfers, Eisens und/oder Mangans bevorzugt; besonders bevorzugt sind Kupfer-Phthalocyanin-Farbstoffe.Preferably, the agents contain more than 0 wt .-% to 0.01 wt .-%, in particular up to 0.005 wt .-% of colored, especially blue and / or green, metal pigment. Among them, complex compounds of nickel, cobalt, cuprous, iron and / or manganese are preferred; particularly preferred are copper phthalocyanine dyes.

Die StabilitƤt sowohl des farbigen Metallpigments wie auch des Alkalihypochlorits wird durch die Anwesenheit von Alkalijodid erhƶht. Vorzugsweise sind mehr als 0 Gew.-% bis hin zu etwa 0,01 Gew.-%, insbesondere etwa 0,0005 Gew.-% bis zu etwa 0,003 Gew.-% Alkalijodid, insbesondere Kaliumjodid, vorhanden.The stability of both the colored metal pigment and the alkali hypochlorite is enhanced by the presence of alkali iodide. Preferably, more than 0 wt% to about 0.01 wt%, more preferably about 0.0005 wt% to about 0.003 wt% alkali iodide, especially potassium iodide is present.

Die erfindungsgemƤƟ stabilisierten Mittel sind normalerweise alkalisch und kƶnnen zu diesem Zweck etwa 0,1 Gew.-% bis 2 Gew.-%, insbesondere 0,1 Gew.-% bis 1,1 Gew.-% Alkalihydroxid enthalten. Das bevorzugte Alkalihydroxid ist Natriumhydroxid, und auch die Alkalisalze, die im Zusammenhang mit den Ć¼brigen Inhaltsstoffen der Mittel genannt werden, sind vorzugsweise die Natriumsalze.The stabilized agents according to the invention are normally alkaline and may contain for this purpose about 0.1 wt .-% to 2 wt .-%, in particular 0.1 wt .-% to 1.1 wt .-% alkali metal hydroxide. The preferred alkali hydroxide is sodium hydroxide, and also the alkali salts mentioned in connection with the other ingredients of the compositions are preferably the sodium salts.

Die Zubereitungen kƶnnen Tenside enthalten, die in Gegenwart des Hypochlorits stabil sind. Bevorzugt sind Betaine, insbesondere der allgemeinen Formel II,

Figure imgb0003
in der R7 eine Alkyl- oder Alkenylgruppe mit 6 bis 22 Kohlenstoffatomen oder eine Gruppe R10CO-NH-(CH2)n- ist, R8 Wasserstoff oder eine Alkylgruppe mit 1 bis 4 Kohlenstoffatomen ist, R9 Wasserstoff oder eine Alkylgruppe mit 1 bis 4 Kohlenstoffatomen ist, R10 eine Alkyl- oder Alkenylgruppe mit 6 bis 22 Kohlenstoffatomen ist, m eine Zahl von 1 bis 6 und n eine Zahl von 1 bis 3 ist. Beispiele fĆ¼r besonders geeignete Vertreter dieser Klasse von Tensiden umfassen C12-18-Alkyl-dimethylbetain, kommerziell erhƤltlich als KokosnuƟbetain, und C10-16-Alkyl-dimethylbetain, kommerziell erhƤltlich als Laurylbetain. Eine weitere Klasse besonders bevorzugter Tenside sind die Alkylethersulfate, die durch Umsetzung von Alkoholen (vorzugsweise mit 6 bis 22 Kohlenstoffatomen) mit Alkylenoxiden, insbesondere Ethylenoxid, und anschlieƟende Sulfatierung und Neutralisation erhƤltlich sind, insbesondere ein mit 2 Equivalenten Ethylenoxid alkoxyliertes C12-14-Fettalkoholethersulfat. In den Ethersulfaten ist das korrespondierende Kation vorzugsweise Natrium. Tenside sind, falls anwesend, vorzugsweise in Mengen bis zu 5 Gew.-%, insbesondere von 0,01 Gew.-% bis 3 Gew.-% in erfindungsgemƤƟ stabilisierten Mitteln enthalten.The formulations may contain surfactants that are stable in the presence of the hypochlorite. Preference is given to betaines, in particular of the general formula II,
Figure imgb0003
wherein R 7 is an alkyl or alkenyl group having 6 to 22 carbon atoms or a group R 10 is CO-NH- (CH 2 ) n -, R 8 is hydrogen or an alkyl group having 1 to 4 carbon atoms, R 9 is hydrogen or an alkyl group having 1 to 4 carbon atoms, R 10 is an alkyl or alkenyl group having 6 to 22 carbon atoms, m is a number from 1 to 6 and n is a number 1 to 3 Examples of particularly suitable members of this class of surfactants include C 12-18 alkyl dimethyl betaine, commercially available as coconut betaine, and C 10-16 alkyl dimethyl betaine, commercially available as lauryl betaine. Another class of particularly preferred surfactants are the alkyl ether sulfates obtainable by reacting alcohols (preferably having 6 to 22 carbon atoms) with alkylene oxides, especially ethylene oxide, followed by sulfation and neutralization, especially a C 12-14 fatty alcohol ether sulfate alkoxylated with 2 equivalents of ethylene oxide , In the ether sulfates, the corresponding cation is preferably sodium. Surfactants, if present, are preferably contained in amounts of up to 5% by weight, in particular of 0.01% by weight to 3% by weight, of stabilizers in accordance with the invention.

Die Zubereitungen kƶnnen zusƤtzlich Sequestriermittel enthalten, vorzugsweise AlkylphosphonsƤuren und unter diesen insbesondere solche mit zumindest einem Aminoxid-Substituenten an der Alkylgruppe, hier als AminoxidphosphonsƤuren bezeichnet, PolyacrylsƤuren und/oder Phosphonogruppen-aufweisende PolyacrysƤuren, die auch in der Form ihrer Alkalisalze vorliegen kƶnnen. Die Einarbeitung derartiger Komplexbildner fĆ¼hrt Ć¼berraschenderweise zu besonders gutem Glanzerhalt der behandelten harten OberflƤchen. Dies wird nicht beobachtet, wenn man stattdessen andere Komplexbildner, beispielsweise MethylglycindiessigsƤure oder NitrilotriessigsƤure, einsetzt. AminoxidphosphonsƤuren werden normalerweise durch Oxidation von AminoalkylphosphonsƤuren hergestellt. Sie gehƶren vorzugsweise zur Gruppe von Verbindungen gemƤƟ allgemeiner Formel (III),

Figure imgb0004
in der R11 Wasserstoff, eine Gruppe -(CH2)x(CHCH3)y-NH2->O oder ein Alkalimetall ist, x eine Zahl von 1 bis 4 und y 0 oder 1 ist. Unter den besonders bevorzugten AminoxidphosphonsƤuren ist das Aminoxid auf der Basis der AminotrimethylenphosphonsƤure. Vorzugsweise sind 0,01 Gew.-% bis 2 Gew.-% solcher Sequestriermittel vorhanden.The preparations may additionally comprise sequestering agents, preferably alkylphosphonic acids, and among these in particular those having at least one amine oxide substituent on the alkyl group, referred to herein as amine oxide phosphonic acids, polyacrylic acids and / or polyoxyacids containing phosphono groups, which may also be in the form of their alkali metal salts. The incorporation of such complexing leads surprisingly to a particularly good gloss retention of the treated hard surfaces. This is not observed if instead other complexing agents, for example methylglycinediacetic acid or nitrilotriacetic acid, are used. Amine oxide phosphonic acids are normally prepared by oxidation of aminoalkyl phosphonic acids. They preferably belong to the group of Compounds according to general formula (III),
Figure imgb0004
in which R 11 is hydrogen, a group - (CH 2 ) x (CHCH 3 ) y -NH 2 -> O or an alkali metal, x is a number from 1 to 4 and y is 0 or 1. Among the more preferred amine oxide phosphonic acids is the amine oxide based on aminotrimethylene phosphonic acid. Preferably, from 0.01% to 2% by weight of such sequestering agents are present.

ZusƤtzlich zu den genannten Bestandteilen kƶnnen die erfindungsgemƤƟ stabilisierten Zubereitungen geringe Mengen an einem oder mehreren bleichstabilen Riechstoffen enthalten. Die gegebenenfalls enthaltene Duftstoffkomponente ist vorzugsweise von hƶherer relativer FlĆ¼chtigkeit als die Bestandteile, die gegebenenfalls fĆ¼r einen Bleichegeruch verantwortlich sind.In addition to the constituents mentioned, the preparations stabilized according to the invention may contain small amounts of one or more bleach-stable fragrances. The optional perfume component is preferably of higher relative volatility than the ingredients optionally responsible for a bleaching odor.

Die erfindungsgemƤƟ stabilisierten Mittel kƶnnen in einfacher Weise durch Vermischen der obengenannten Inhaltsstoffe in den angegebenen Mengen hergestellt werden.The stabilized compositions according to the invention can be prepared in a simple manner by mixing the above-mentioned ingredients in the indicated amounts.

BeispieleExamples

Die erfindungsgemƤƟe Zubereitung (I1) mit einem hohen Pigmentgehalt und zu Vergleichszwecken Zubereitungen ohne Amin (C1), ohne Kaliumjodid (C2) und ohne beide (C3) wurden durch Vermischen der Inhaltsstoffe mit Wasser hergestellt. Die Mittel waren wie folgt zusammengesetzt [Gew.-%]: I1 C1 C2 C3 Natriumhypochlorit 4 4 4 4 C12/14-Fettalkohol 2 EO sulfat, Natriumsalz 1,2 1,2 1,2 1,2 Amina) 0,01 - 0,01 - Kaliumjodid 0,001 0,001 - - Cu-Phthalocyanin 0,005 0,005 0,005 0,005 Natriumhydroxid 1 1 1 1 Wasser auf 100 auf 100 auf 100 auf 100 a) 2,2,6,6-Tetramethyl-4-hydroxypiperidin-N-oxid The preparation (I1) according to the invention with a high pigment content and for comparison purposes preparations without amine (C1), without potassium iodide (C2) and without both (C3) were prepared by mixing the ingredients with water. The compositions were composed as follows [wt%]: I1 C1 C2 C3 sodium hypochlorite 4 4 4 4 C 12/14 fatty alcohol 2 EO sulfate, sodium salt 1.2 1.2 1.2 1.2 Amine a) 0.01 - 0.01 - potassium iodide 0.001 0.001 - - Cu phthalocyanine 0.005 0.005 0.005 0.005 sodium hydroxide 1 1 1 1 water on 100 on 100 on 100 on 100 a) 2,2,6,6-tetramethyl-4-hydroxypiperidine N-oxide

Alle Mittel wurden in Plastikflaschen abgefĆ¼llt und fĆ¼r mehrere Wochen gelagert. In der erfindungsgemƤƟen Zubereitungen war der Hypochloritgehalt nach Lagerung deutlich hƶher als in den zum Vergleich getesteten Zubereitungen. AuƟerdem war der Druck in der Flasche des Mittels C3 (vermutlich wegen der Bildung von Sauerstoff) nach nur 4 Tagen bei 60 Ā°C auf ca. 100 Kp angestiegen, wohingegen der Druck beim erfindungsgemƤƟen Mittel auch nach lƤngerer Zeit noch bei unter 20 Kp lag.All funds were bottled in plastic bottles and stored for several weeks. In the preparations according to the invention, the hypochlorite content after storage was significantly higher than in the preparations tested for comparison. In addition, the pressure in the bottle of the agent C3 (presumably because of the formation of oxygen) after only 4 days at 60 Ā° C to about 100 Kp had increased, whereas the pressure in the inventive agent even after a long time was less than 20 Kp.

Claims (11)

  1. Combined use of an alkali iodide and of a sterically hindered amine that comprises the group having the general formula (I)
    Figure imgb0007
    in which the radicals R1, R2, R3, and R4, mutually independently, denote hydrogen, a methyl group, or an ethyl group, with the stipulation that no more than two of said radicals are simultaneously hydrogen, and X denotes hydrogen, oxygen, a methyl group, an ethyl group, -OH, or -OR5, R5 being a C1-4 alkyl group or a cyclohexyl group, for stabilizing hypochlorite-containing aqueous liquid compositions that contain colored metal pigment.
  2. The use according to Claim 1, wherein in the sterically hindered amine, the group of the general formula (I) is part of a piperidine ring.
  3. The use according to Claim 2, wherein in the sterically hindered amine, the piperidine ring comprises, in addition to the substituents R1, R2, R3, R4, and X, a substituent in position 4 that is -OH, -NHR6, or oxygen joined via a double bond, R6 being a C1-4 alkyl group or a cyclohexyl group.
  4. The use according to one of Claims 1 to 3, wherein the composition contains more than 0 wt% to 0.01 wt%, in particular 0.0005 wt% to 0.003 wt%, alkali iodide, in particular potassium iodide.
  5. The use according to one of Claims 1 to 4, wherein the composition contains more than 0 wt% to 0.1 wt%, in particular 0.0005 wt% to 0.03 wt%, of the sterically hindered amine.
  6. The use according to one of Claims 1 to 5, wherein the composition contains more than 0 wt% to 0.01 wt%, in particular up to 0.005 wt%, colored metal pigment.
  7. The use according to one of Claims 1 to 6, wherein the metal pigment is a copper phthalocyanine dye.
  8. The use according to one of Claims 1 to 7, wherein the composition contains 0.5 wt% to 5 wt% alkali hypochlorite, in particular sodium hypochlorite.
  9. The use according to one of Claims 1 to 8, wherein the composition contains up to 5 wt% bleach-stable surfactant, in particular betaine and/or alkyl ether sulfate.
  10. The use according to one of Claims 1 to 9, wherein the composition contains 0.01 wt% to 2 wt% alkylphosphonic acid and/or alkylphosphonate, in particular amine oxide phosphonic acid, polyacrylic acid, polyacrylic acid containing phosphono groups, and/or an alkali salt of one, two, or all three of said acids.
  11. An aqueous liquid bleaching agent containing alkali hypochlorite and colored metal pigment, wherein it additionally contains a combination of alkali iodide and sterically hindered amine that comprises the group having the general formula (I)
    Figure imgb0008
    in which the radicals R1, R2, R3, and R4, mutually independently, denote hydrogen, a methyl group, or an ethyl group, with the stipulation that no more than two of said radicals are simultaneously hydrogen, and X denotes hydrogen, oxygen, a methyl group, an ethyl group, -OH, or -OR5, R5 being a C1-4 alkyl group or a cyclohexyl group.
EP06818842A 2005-12-06 2006-11-27 Stability improvement of liquid hypochlorite-containing washing and cleaning compositions Not-in-force EP1957621B1 (en)

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PCT/EP2006/011348 WO2007065581A1 (en) 2005-12-06 2006-11-27 Stability improvement of liquid hypochlorite-containing washing and cleaning compositions

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ES2353976T3 (en) 2011-03-08
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ATE483786T1 (en) 2010-10-15
PL1957621T3 (en) 2011-04-29
DE102005058339A1 (en) 2007-06-28
EP1957621A1 (en) 2008-08-20
WO2007065581A1 (en) 2007-06-14

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