EP0696314A1 - Agents for use in the machine-cleaning and disinfection of textiles - Google Patents
Agents for use in the machine-cleaning and disinfection of textilesInfo
- Publication number
- EP0696314A1 EP0696314A1 EP94915111A EP94915111A EP0696314A1 EP 0696314 A1 EP0696314 A1 EP 0696314A1 EP 94915111 A EP94915111 A EP 94915111A EP 94915111 A EP94915111 A EP 94915111A EP 0696314 A1 EP0696314 A1 EP 0696314A1
- Authority
- EP
- European Patent Office
- Prior art keywords
- weight
- agents
- component
- cleaning
- monobutyl ether
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Withdrawn
Links
Classifications
-
- 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
- C11D3/48—Medical, disinfecting agents, disinfecting, antibacterial, germicidal or antimicrobial compositions
-
- 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
- C11D1/00—Detergent compositions based essentially on surface-active compounds; Use of these compounds as a detergent
- C11D1/66—Non-ionic compounds
- C11D1/722—Ethers of polyoxyalkylene glycols having mixed oxyalkylene groups; Polyalkoxylated fatty alcohols or polyalkoxylated alkylaryl alcohols with mixed oxyalkylele groups
-
- 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
- C11D3/16—Organic compounds
- C11D3/20—Organic compounds containing oxygen
- C11D3/2068—Ethers
Definitions
- R represents a linear alkyl radical having 12-14 carbon atoms, with compounds of the formula
- R 1 denotes an alkyl radical with 1 to 4 carbon atoms or a hydrogen atom, the molar ratio of the two reaction partners being 1: 1 to 1: 2.
- the reaction products also called component U
- ethylene oxide or propylene oxide and / or with inorganic or organic acids can be used, inter alia, as additives to cleaning and disinfecting agents for textiles, for example in laundries.
- organic solvents in particular alcohols and glycol ethers, can be used as solvents besides water. Diethylene glycol monobutyl ethers are not mentioned.
- Propoxylated fatty alcohol ethoxylates are also not proposed as surfactants.
- WO 91/13965 discloses aqueous compositions for cleaning and disinfecting objects from medical facilities which contain the abovementioned antimicrobial substances and one or more organic substances.
- African solvents in particular lower alcohols, glycols and glycol ethers, including diethylene glycol monobutyl ether.
- this ether is also combined with a propoxylated fatty alcohol ethoxylate, the recipe given contains so many further constituents that the teaching of the present invention could not be derived from it.
- the use of such agents for cleaning and disinfecting textiles in washing machines is also not mentioned there.
- isopropanol or 1,2-propylene glycol are used as solubilizers in the assembly of component U in liquid agents.
- the agents thus assembled are thus easy to convey and dose, which in particular guarantees their good applicability in fully automatic machines in commercial laundries. In this way, the valuable properties of the antimicrobial agent can also be used for disinfection for textiles.
- nonionic surfactants such as, for example, a 6-20 mole ethylene oxide and subsequently C 1 -C 4 -o-xo alcohol (Plurafac ( R ) LF 220) end-capped with butylene glycol, a C 1 -C reaction with 6.4 mole ethylene oxide and 1.2 mole propylene oxide Ci4 fatty alcohol (Dehypon ( R ) 980), a Ci4 / i5 fatty alcohol (Dobanol ( R ) 45/4) reacted with 4 mol ethylene oxide, an isotridecyl alcohol (Lutensol ( R ) T03) reacted with 3 mol ethylene oxide or a reaction product end-capped with butylene glycol from a Ci2-Ci4 fatty alcohol and 10 mol ethylene oxide (Dehypon ( R ) LS 104) did not lead to the results according to the invention.
- Plurafac ( R ) LF 220 C 1 -C 4 -o-xo alcohol
- the amount of component U in the cleaning agents is about 15 to 60, preferably about 35 to 55% by weight.
- the surfactant is used in amounts from about 10 to about 30, preferably from about 12 to 20,% by weight.
- the amount of diethylene glycol monobutyl ether is about 10 to 30, preferably about 15 to 20 wt .-%, the rest, which is missing up to 100 wt .-%, consists of water, the total proportion of about 20 to 40, preferably about 25 to 35 wt .-%.
- foam regulators can also be added to the cleaning and disinfectants, such as silicone oils, paraffins, Ci2-C * i8 fatty alcohol + x E0 + y PO; BASF (Plurafac ( R ) LF 403), phosphoric acid mono- / distearyl ester or a reaction product capped with butylene glycol from a Ci2-Ci8 fatty alcohol and 9 mol E0 (Dehypon ( R ) LT 104).
- Their amounts should not be more than about 5% by weight, preferably about 0.5 to 2.0% by weight.
- the agents are produced by combining and mixing the individual components.
- the pH of the undiluted solutions is about 8.7, in concentrations of 1% by weight about 9.8.
- the cleaning and disinfectants according to the invention can also be used in aqueous dilution at concentrations of about 0.5 to 6% by weight at 60 ° C. and from about 6 to 12% by weight at 40 ° C. for washing and disinfection and cleaning can be used.
- concentrations of about 0.5 to 6% by weight at 60 ° C. and from about 6 to 12% by weight at 40 ° C. for washing and disinfection and cleaning can be used.
- the bacteriological and virucidal activity met expectations.
- component U 15.0% by weight of Ci2-Ci4-alkanol + 5 E0 + 4 PO 17.0% by weight of diethylene glycol monobutyl ether 25.5% by weight of water
- the composition has a very good washing effect and an equally good wetting effect.
- the viscosity behavior is hardly changed by temperature fluctuations between approximately minus 10 ° C. and approximately plus 40 ° C. and even after storage for 6 months there were no signs of segregation and no crystallization of component U.
- composition has a good washing or wetting effect, it becomes significantly more viscous after storage and leads to significant clouding after one week.
- component U 50% active substance
- Ci2-Ci4-alkanol + 5 E0 + 5 PO 17.0% by weight of isopropanol 25.5% by weight of water
- the composition has good washing and wetting effects, but has a very low flash point (30 ° C) and low cloud point.
- component U (50% active substance) 15.0% by weight of isotridecyl + 3 E0 (Lutensol ( R ) T03) 17.0% by weight of diethylene glycol monobutyl ether
- composition has a good washing or wetting effect, it is firm after a week and therefore cannot be metered.
- Ci4-Ci5 alkanol + 4 E0 Dobanol ( R ) 45/4) 17.0% by weight of diethylene glycol monobutyl ether 25.5% by weight of water
- composition has good washing and wetting effects, it is solid after one week of storage and can therefore no longer be metered.
- composition has good washing and wetting effects, it leads to clouding after storage, which makes dosing by suction dancing impossible.
- composition has good washing and wetting effects, it is solid after one week of storage and can therefore no longer be metered.
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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)
- Health & Medical Sciences (AREA)
- Emergency Medicine (AREA)
- Detergent Compositions (AREA)
- Agricultural Chemicals And Associated Chemicals (AREA)
Abstract
Described are agents for machine-cleaning and disinfecting textiles, the agents consisting of an aqueous solution of antimicrobially active substances obtained by reacting N-substituted propylene diamines of the formula (I): R-NH-CH2-CH2-CH2-NH2, in which R is a straight-chain alkyl group with 12 to 14 carbon atoms, with compounds of formula (I), in which R1 is an alkyl group with 1 to 4 carbon atoms or a hydrogen atom, the molar ratio of the two reactants being between 1:1 and 1:2 (component U), plus a C12-C14 alkanol, plus 5 moles of ethylene oxide and 4 moles of propylene oxide, plus diethyleneglycol monobutyl ether.
Description
"Mittel zur maschinellen Reinigung und Desinfektion von Textilien" "Means for machine cleaning and disinfection of textiles"
Aus der europäischen Patentschrift 156 275 sind antimikrobiell wirksame Substanzen bekannt, die etwa durch Umsetzen von n-substituierten Propylen- diaminen der FormelFrom European patent specification 156 275 antimicrobial substances are known, for example by reacting n-substituted propylene diamines of the formula
R-NH-CH2-CH2-CH2-NH2,R-NH-CH 2 -CH2-CH 2 -NH2,
in der R für einen linearen Alkylrest mit 12 - 14 Kohlenstoffatomen steht, mit Verbindungen der Formelin which R represents a linear alkyl radical having 12-14 carbon atoms, with compounds of the formula
R1-O-CO-CH2-CH2-CH-COOHR1-O-CO-CH2-CH2-CH-COOH
II.
NH2,NH 2 ,
in der R^ einen Alkylrest mit 1 - 4 Kohlenstoffatomen oder ein Wasser¬ stoffatom bedeutet, wobei das molare Verhältnis der beiden Reaktionspart¬ ner 1 : 1 bis 1 : 2 beträgt, erhältlich sind. Die Umsetzungsprodukte (wei¬ terhin Komponente U genannt) können gegebenenfalls weiter mit Ethylen- oder Propylenoxid und/oder mit anorganischen oder organischen Säuren um¬ gesetzt werden. Derartige Mittel sind unter anderem als Zusätze zu Reini- gungs- und Desinfektionsmitteln für Textilien beispielsweise in Wäsche¬ reien zu gebrauchen. Weiterhin ist hiernach bekannt, daß man für flüssige Tensidzubereitungen derartiger Mittel als Lösungsmittel außer Wasser üb¬ liche organische Lösungsmittel, insbesondere Alkohole und Glykolether ver¬ wenden kann. Diethylenglykolmonobutylether werden nicht genannt. Auch pro- poxylierte Fettalkoholethoxylate werden nicht als Tenside vorgeschlagen. Aus der WO 91/13965 sind wäßrige Mittel zur Reinigung und Desinfektion von Gegenständen aus medizinischen Einrichtungen bekannt, die die vorstehend genannten antimikrobiell wirksamen Substanzen sowie ein oder mehrere orga-
nische Lösungsmittel, insbesondere niedere Alkohole Glykole und Glykol- ether, unter anderem auch Diethylenglykolmonobutylether enthalten. Zwar wird dieser Ether auch mit einem propoxylierten Fettalkoholethoxylat kom¬ biniert, aber die angegebene Rezeptur enthält so viele weitere Bestand¬ teile, daß die Lehre der vorliegenden Erfindung daraus nicht abgeleitet werden konnte. Die Verwendung derartiger Mittel zur Reinigung und Desin¬ fektion von Textilien in Waschmaschinen wird dort ebenfalls nicht erwähnt. Im allgemeinen werden bei der Konfektionierung der Komponente U in flüs¬ sigen Mitteln Isopropanol oder 1,2-Propylenglykol als Lösungsvermittler verwendet.in which R 1 denotes an alkyl radical with 1 to 4 carbon atoms or a hydrogen atom, the molar ratio of the two reaction partners being 1: 1 to 1: 2. If appropriate, the reaction products (also called component U) can be reacted further with ethylene oxide or propylene oxide and / or with inorganic or organic acids. Such agents can be used, inter alia, as additives to cleaning and disinfecting agents for textiles, for example in laundries. It is also known hereafter that, for liquid surfactant preparations of such compositions, organic solvents, in particular alcohols and glycol ethers, can be used as solvents besides water. Diethylene glycol monobutyl ethers are not mentioned. Propoxylated fatty alcohol ethoxylates are also not proposed as surfactants. WO 91/13965 discloses aqueous compositions for cleaning and disinfecting objects from medical facilities which contain the abovementioned antimicrobial substances and one or more organic substances. African solvents, in particular lower alcohols, glycols and glycol ethers, including diethylene glycol monobutyl ether. Although this ether is also combined with a propoxylated fatty alcohol ethoxylate, the recipe given contains so many further constituents that the teaching of the present invention could not be derived from it. The use of such agents for cleaning and disinfecting textiles in washing machines is also not mentioned there. In general, isopropanol or 1,2-propylene glycol are used as solubilizers in the assembly of component U in liquid agents.
Bei der Herstellung vertriebsfertiger Reinigungs- und Desinfektionsmittel für Textilien in Waschmaschinen wurde nun gefunden, daß man zu deutlich besseren Ergebnissen kommt, wenn man bei Gemischen aus nichtionischen Ten- siden und antimikrobiellen Wirkstoffen gemäß Komponente U in Wasser als nichtionisches Tensid Ci2-C*i4-Alkanol, umgesetzt mit 5 Mol Ethylenoxid (EO) und anschließend 4 Mol Propylenoxid (PO) (Dehypon(R) LS 54) und als Lösungsvermittler anstelle von Isopropanol oder 1,2-Propylenglykol Diethy¬ lenglykolmonobutylether verwendet. Die Rezepturen bleiben dann auch nach längerer Lagerzeit klar und dünnflüssig und weisen keinerlei Trübungen auf, wobei sich die Viskosität der Mittel in Abhängigkeit von der Tempera¬ tur kaum ändert. Auch nach mehrmonatiger Lagerung im Klimaschrank bei wechselnden Temperaturen zwischen minus 10 °C und plus 40 °C bleiben sie stabil und erleiden keine Phasentrennungen. Die auf diese Weise konfekti¬ onierten Mittel sind damit leicht zu fördern und zu dosieren, was insbe¬ sondere ihre gute Anwendbarkeit in vollautomatisch arbeitenden Maschinen in gewerblichen Wäschereien garantiert. Auf diese Weise lassen sich die wertvollen Eigenschaften des antimikrobiellen Mittels auch für die Desin¬ fektion für Textilien nutzen.In the manufacture of ready-to-sell cleaning and disinfectants for textiles in washing machines, it has now been found that significantly better results are obtained if mixtures of nonionic surfactants and antimicrobial active ingredients according to component U in water are used as the nonionic surfactant Ci2-C * i4- Alkanol, reacted with 5 mol of ethylene oxide (EO) and then 4 mol of propylene oxide (PO) (Dehypon ( R ) LS 54) and used as a solubilizer instead of isopropanol or 1,2-propylene glycol diethylene glycol monobutyl ether. The formulations then remain clear and thin even after a long storage period and have no cloudiness, the viscosity of the agents hardly changing as a function of the temperature. Even after several months of storage in a climatic cabinet with changing temperatures between minus 10 ° C and plus 40 ° C, they remain stable and do not suffer any phase separations. The agents thus assembled are thus easy to convey and dose, which in particular guarantees their good applicability in fully automatic machines in commercial laundries. In this way, the valuable properties of the antimicrobial agent can also be used for disinfection for textiles.
Andere nichtionische Tenside, wie beispielsweise ein mit 6 - 20 Mol Ethy¬ lenoxid und anschließend mit Butylenglykol endgruppenverschlossener Cιo~ Ci4-0xoalkohol (Plurafac(R) LF 220), ein mit 6,4 Mol Ethylenoxid und 1,2 Mol Propylenoxid umgesetzter Cιo-Ci4-Fettalkohol (Dehypon(R) 980), ein mit 4 Mol Ethylenoxid umgesetzter Ci4/i5-Fettalkohol (Dobanol(R) 45/4), ein mit 3 Mol Ethylenoxid umgesetzter Isotridecylalkohol (Lutensol(R) T03)
oder ein mit Butylenglykol endgruppenverschlossenes Umsetzungsprodukt aus einem Ci2-Ci4-Fettalkohol und 10 Mol Ethylenoxid (Dehypon(R) LS 104) führ¬ ten nicht zu den erfindungsgemäßen Ergebnissen.Other nonionic surfactants, such as, for example, a 6-20 mole ethylene oxide and subsequently C 1 -C 4 -o-xo alcohol (Plurafac ( R ) LF 220) end-capped with butylene glycol, a C 1 -C reaction with 6.4 mole ethylene oxide and 1.2 mole propylene oxide Ci4 fatty alcohol (Dehypon ( R ) 980), a Ci4 / i5 fatty alcohol (Dobanol ( R ) 45/4) reacted with 4 mol ethylene oxide, an isotridecyl alcohol (Lutensol ( R ) T03) reacted with 3 mol ethylene oxide or a reaction product end-capped with butylene glycol from a Ci2-Ci4 fatty alcohol and 10 mol ethylene oxide (Dehypon ( R ) LS 104) did not lead to the results according to the invention.
Die Menge an Komponente U in den Reinigungsmitteln beträgt etwa 15 bis 60, vorzugsweise etwa 35 bis 55 Gew.-%. Das Tensid wird in Mengen von etwa 10 bis etwa 30, vorzugsweise von etwa 12 bis 20 Gew.-% eingesetzt. Die Menge an Diethylenglykolmonobutylether beträgt etwa 10 bis 30, vorzugsweise etwa 15 - 20 Gew.-%, der Rest, der jeweils bis 100 Gew.-% fehlt, besteht aus Wasser, dessen Gesamtanteil etwa 20 bis 40, vorzugsweise etwa 25 bis 35 Gew.-% beträgt. Gegebenenfalls können den Reinigungs- und Desinfektions¬ mitteln auch noch Schaumregulatoren zugesetzt werden wie beispielsweise Silikonöle, Paraffine, Ci2-C*i8-Fettalkohol + x E0 + y PO; BASF (Plura- fac(R) LF 403), Phosphorsäuremono-/distearylester oder ein mit Butylengly¬ kol endgruppenverschlossenes Umsetzungsprodukt aus einem Ci2-Ci8-Fettal- kohol und 9 Mol E0 (Dehypon(R) LT 104). Ihre Mengen sollen nicht mehr als etwa 5 Gew.-%, vorzugsweise etwa 0,5 bis 2,0 Gew.-% betragen. Die Mittel werden durch Zusammengeben und Vermischen der einzelnen Bestandteile her¬ gestellt. Der pH-Wert der unverdünnten Lösungen liegt bei etwa 8,7, in Konzentrationen von 1 Gew.-% etwa bei 9,8. Die erfindungsgemäßen Reini¬ gungs- und Desinfektionsmittel können auch in wäßriger Verdünnung bei Kon¬ zentrationen von etwa 0,5 bis 6 Gew.-% bei 60 °C und von etwa 6 bis 12 Gew.-% bei 40 °C zur Wäsche, Desinfektion und Reinigung verwendet werden. Die bakteriologische und viruzide Wirksamkeit entsprach den Erwartungen.
The amount of component U in the cleaning agents is about 15 to 60, preferably about 35 to 55% by weight. The surfactant is used in amounts from about 10 to about 30, preferably from about 12 to 20,% by weight. The amount of diethylene glycol monobutyl ether is about 10 to 30, preferably about 15 to 20 wt .-%, the rest, which is missing up to 100 wt .-%, consists of water, the total proportion of about 20 to 40, preferably about 25 to 35 wt .-%. If necessary, foam regulators can also be added to the cleaning and disinfectants, such as silicone oils, paraffins, Ci2-C * i8 fatty alcohol + x E0 + y PO; BASF (Plurafac ( R ) LF 403), phosphoric acid mono- / distearyl ester or a reaction product capped with butylene glycol from a Ci2-Ci8 fatty alcohol and 9 mol E0 (Dehypon ( R ) LT 104). Their amounts should not be more than about 5% by weight, preferably about 0.5 to 2.0% by weight. The agents are produced by combining and mixing the individual components. The pH of the undiluted solutions is about 8.7, in concentrations of 1% by weight about 9.8. The cleaning and disinfectants according to the invention can also be used in aqueous dilution at concentrations of about 0.5 to 6% by weight at 60 ° C. and from about 6 to 12% by weight at 40 ° C. for washing and disinfection and cleaning can be used. The bacteriological and virucidal activity met expectations.
B e i s p i e l eB e i s p i e l e
1. 42,5 Gew.-% Komponente U (50 % Aktivsubstanz) 15,0 Gew.-% Ci2-Ci4-Alkanol + 5 E0 + 4 PO 17,0 Gew.-% Diethylenglykolmonobutylether 25,5 Gew.-% Wasser1. 42.5% by weight of component U (50% active substance) 15.0% by weight of Ci2-Ci4-alkanol + 5 E0 + 4 PO 17.0% by weight of diethylene glycol monobutyl ether 25.5% by weight of water
Die Zusammensetzung verfügt über eine sehr gute Waschwirkung und eine ebenso gute Netzwirkung. Das Viskositätsverhalten wird durch Tempera¬ turschwankungen zwischen etwa minus 10 °C und etwa plus 40 °C kaum verändert und auch nach einer Lagerung von 6 Monaten traten keine Ent¬ mischungserscheinungen und kein Auskristallisieren der Komponente U auf.The composition has a very good washing effect and an equally good wetting effect. The viscosity behavior is hardly changed by temperature fluctuations between approximately minus 10 ° C. and approximately plus 40 ° C. and even after storage for 6 months there were no signs of segregation and no crystallization of component U.
la. 42,5 Gew.-% Komponente U (50 % Aktivsubstanz)la. 42.5% by weight of component U (50% of active substance)
15,0 Gew.-% Ci2-Ci4-Alkanol + 10 EO-Butylether (Dehypon(R) LS 104) 17,0 Gew.-% Diethylenglykolmonobutylether 25,5 Gew.- Wasser15.0% by weight of Ci2-Ci4-alkanol + 10 EO-butyl ether (Dehypon ( R ) LS 104) 17.0% by weight of diethylene glycol monobutyl ether 25.5% by weight of water
Die Zusammensetzung verfügt zwar über gute Wasch- bzw. Netzwirkung, wird jedoch nach Lagerung deutlich viskoser und führt nach einer Woche zu deutlichen Austrübungen.Although the composition has a good washing or wetting effect, it becomes significantly more viscous after storage and leads to significant clouding after one week.
Ib. 42,5 Gew.-% Komponente U (50 % Aktivsubstanz) 15,0 Gew.-% Ci2-Ci4-Alkanol + 5 E0 + 5 PO 17,0 Gew.-% Isopropanol 25,5 Gew.-% WasserIb. 42.5% by weight of component U (50% active substance) 15.0% by weight of Ci2-Ci4-alkanol + 5 E0 + 5 PO 17.0% by weight of isopropanol 25.5% by weight of water
Die Zusammensetzung verfügt zwar über gute Wasch- und Netzwirkung, hat jedoch sehr niedrigen Flammpunkt (30 °C) und niedrigen Trübungspunkt.The composition has good washing and wetting effects, but has a very low flash point (30 ° C) and low cloud point.
2. 42,5 Gew.-% Komponente U (50 % Aktivsubstanz) 15,0 Gew.-% Isotridecyl + 3 E0 (Lutensol(R) T03) 17,0 Gew.-% Diethylenglykolmonobutylether2. 42.5% by weight of component U (50% active substance) 15.0% by weight of isotridecyl + 3 E0 (Lutensol ( R ) T03) 17.0% by weight of diethylene glycol monobutyl ether
25,5 Gew.- Wasser
Die Zusammensetzung verfügt zwar über gute Wasch- bzw. Netzwirkung, ist jedoch nach einer Woche fest und ist damit nicht dosierbar.25.5% water Although the composition has a good washing or wetting effect, it is firm after a week and therefore cannot be metered.
3. 42,5 Gew.-% Komponente U (50 % Aktivsubstanz)3. 42.5% by weight of component U (50% of active substance)
15,0 Gew.- Ci4-Ci5 Alkanol + 4 E0 (Dobanol(R) 45/4) 17,0 Gew.-% Diethylenglykolmonobutylether 25,5 Gew.-% Wasser15.0% by weight of Ci4-Ci5 alkanol + 4 E0 (Dobanol ( R ) 45/4) 17.0% by weight of diethylene glycol monobutyl ether 25.5% by weight of water
Die Zusammensetzung verfügt zwar über gute Wasch- und Netzwirkung, ist jedoch nach einer Woche Lagerung fest und damit nicht mehr dosierbar.Although the composition has good washing and wetting effects, it is solid after one week of storage and can therefore no longer be metered.
4. 42,5 Gew.-% Komponente U (50 % Aktivsubstanz)4. 42.5% by weight of component U (50% of active substance)
15,0 Gew.-% Ci2-Cχ8-(0xo)Alkohol + 6 - 20 Butylenglykol (Plurafac(R)15.0% by weight Ci2-Cχ8- (0xo) alcohol + 6 - 20 butylene glycol (Plurafac ( R )
LF 220) 17,0 Gew.-% Diethylenglykolmonobutylether 25,5 Gew.-% WasserLF 220) 17.0% by weight diethylene glycol monobutyl ether 25.5% by weight water
Die Zusammensetzung verfügt zwar über gute Wasch- und Netzwirkung, führt jedoch nach Lagerung zu Austrübungen, die eine Dosierung über SaugTanzen unmöglich machen.Although the composition has good washing and wetting effects, it leads to clouding after storage, which makes dosing by suction dancing impossible.
5. 42,5 Gew.-% Komponente U5. 42.5% by weight of component U
15,0 Gew.-% Cιo-Ci4-Alkanol + 6,4 E0, 1,2 PO (Dehydol(R) 980) 17,0 Gew.-% Diethylenglykolmonobutylether 25,5 Gew.-% Wasser15.0 wt .-% Cιo-Ci4-alkanol + 6.4 E0, 1.2 PO (Dehydol ( R ) 980) 17.0 wt .-% diethylene glycol monobutyl ether 25.5 wt .-% water
Die Zusammensetzung verfügt zwar über gute Wasch- und Netzwirkung, ist jedoch nach einer Woche Lagerung fest und damit nicht mehr dosierbar.
Although the composition has good washing and wetting effects, it is solid after one week of storage and can therefore no longer be metered.
Claims
1. Mittel zur maschinellen Reinigung und Desinfektion von Textilien, da¬ durch gekennzeichnet, daß es aus einer wäßrigen Lösung von antimikro¬ biellen Wirksubstanzen, die durch Umsetzen von n-substituierten Propy- lendiaminen der Formel1. Means for machine cleaning and disinfection of textiles, characterized in that it consists of an aqueous solution of antimicrobial active substances by reacting n-substituted propylene diamines of the formula
R-NH-CH2-CH2-CH2-NH2,R-NH-CH2-CH2-CH2-NH2,
in der R für einen linearen Alkylrest mit 12 - 14 Kohlenstoffatomen steht, mit Verbindungen der Formelin which R represents a linear alkyl radical having 12-14 carbon atoms, with compounds of the formula
R1-O-CO-CH2-CH2-CH-COOHR1-O-CO-CH2-CH2-CH-COOH
II.
NH2l NH 2l
in der Rj einen Alkylrest mit 1 - 4 Kohlenstoffatomen oder ein Wasser¬ stoffatom bedeutet, wobei das molare Verhältnis der beiden Reaktions¬ partner 1 : 1 bis 1 : 2 beträgt, erhältlich sind (Komponente U), (42- ( 4-Alkanol + 5 EO + 4 PO und Diethylenglykolmonobutylether besteht.in which R 1 denotes an alkyl radical with 1-4 carbon atoms or a hydrogen atom, the molar ratio of the two reaction partners being 1: 1 to 1: 2, (component U), (42- (4-alkanol + 5 EO + 4 PO and diethylene glycol monobutyl ether.
2. Mittel nach Anspruch 1, dadurch gekennzeichnet, daß es aus einer wä߬ rigen Lösung von etwa 15 bis 60, vorzugsweise etwa 35 bis 55 Gew.-% der Komponente U, etwa 10 bis 30, vorzugsweise etwa 12 bis 20 Gew.-% Ci2-Ci4-Alkanol + 5 EO + 4 PO und etwa 10 bis 30, vorzugsweise etwa 15 bis 20 Gew.-% Diethylenglykolmonobutylether besteht, wobei der Was¬ sergehalt bei etwa 20 bis 40, vorzugsweise etwa 25 bis 35 Gew.-% be¬ trägt. 2. Composition according to claim 1, characterized in that it from an aqueous solution of about 15 to 60, preferably about 35 to 55 wt .-% of component U, about 10 to 30, preferably about 12 to 20 wt .-% % Ci2-Ci4-Alkanol + 5 EO + 4 PO and about 10 to 30, preferably about 15 to 20% by weight diethylene glycol monobutyl ether, the water content being about 20 to 40, preferably about 25 to 35% by weight be¬ contributes.
Applications Claiming Priority (3)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
DE19934314524 DE4314524A1 (en) | 1993-05-03 | 1993-05-03 | Means for machine cleaning and disinfection of textiles |
DE4314524 | 1993-05-03 | ||
PCT/EP1994/001282 WO1994025559A1 (en) | 1993-05-03 | 1994-04-25 | Agents for use in the machine-cleaning and disinfection of textiles |
Publications (1)
Publication Number | Publication Date |
---|---|
EP0696314A1 true EP0696314A1 (en) | 1996-02-14 |
Family
ID=6487012
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
EP94915111A Withdrawn EP0696314A1 (en) | 1993-05-03 | 1994-04-25 | Agents for use in the machine-cleaning and disinfection of textiles |
Country Status (3)
Country | Link |
---|---|
EP (1) | EP0696314A1 (en) |
DE (1) | DE4314524A1 (en) |
WO (1) | WO1994025559A1 (en) |
Families Citing this family (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
DE4340124A1 (en) * | 1993-11-25 | 1995-06-01 | Henkel Ecolab Gmbh & Co Ohg | Virus-active substances |
DE59504287D1 (en) * | 1994-09-26 | 1998-12-24 | Henkel Kgaa | USE OF SURFACES TO INCREASE THE ANTIMICROBIAL EFFECTIVENESS OF A CARBONIC ACID |
Family Cites Families (5)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
DE3410956A1 (en) * | 1984-03-24 | 1985-09-26 | Henkel KGaA, 4000 Düsseldorf | ANTIMICROBIALLY EFFECTIVE SUBSTANCES, THEIR PRODUCTION AND THEIR USE |
ZA876157B (en) * | 1986-08-28 | 1989-04-26 | Colgate Palmolive Co | Nonaqueous liquid nonionic laundry detergent composition and method of use |
DE4007758A1 (en) * | 1990-03-12 | 1991-09-19 | Henkel Kgaa | MEANS AND METHODS FOR CLEANING AND DISINFECTING OBJECTS FROM MEDICAL EQUIPMENT IN AUTOMATED EQUIPMENT |
DE69217516T2 (en) * | 1991-07-15 | 1997-09-11 | Cfpi Ind | Acidic, disinfectant and scale removing detergent and process for its manufacture |
DE4234070A1 (en) * | 1992-10-09 | 1994-04-14 | Henkel Ecolab Gmbh & Co Ohg | Cleaning disinfectant |
-
1993
- 1993-05-03 DE DE19934314524 patent/DE4314524A1/en not_active Withdrawn
-
1994
- 1994-04-25 EP EP94915111A patent/EP0696314A1/en not_active Withdrawn
- 1994-04-25 WO PCT/EP1994/001282 patent/WO1994025559A1/en not_active Application Discontinuation
Non-Patent Citations (1)
Title |
---|
See references of WO9425559A1 * |
Also Published As
Publication number | Publication date |
---|---|
WO1994025559A1 (en) | 1994-11-10 |
DE4314524A1 (en) | 1994-11-10 |
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