EP0385216A1 - Bleaching liquid detergents - Google Patents
Bleaching liquid detergents Download PDFInfo
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- EP0385216A1 EP0385216A1 EP90103139A EP90103139A EP0385216A1 EP 0385216 A1 EP0385216 A1 EP 0385216A1 EP 90103139 A EP90103139 A EP 90103139A EP 90103139 A EP90103139 A EP 90103139A EP 0385216 A1 EP0385216 A1 EP 0385216A1
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- soap
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Classifications
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- C—CHEMISTRY; METALLURGY
- C11—ANIMAL OR VEGETABLE OILS, FATS, FATTY SUBSTANCES OR WAXES; FATTY ACIDS THEREFROM; DETERGENTS; CANDLES
- C11D—DETERGENT COMPOSITIONS; USE OF SINGLE SUBSTANCES AS DETERGENTS; SOAP OR SOAP-MAKING; RESIN SOAPS; RECOVERY OF GLYCEROL
- C11D10/00—Compositions of detergents, not provided for by one single preceding group
- C11D10/04—Compositions of detergents, not provided for by one single preceding group based on mixtures of surface-active non-soap compounds and soap
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- C—CHEMISTRY; METALLURGY
- C11—ANIMAL OR VEGETABLE OILS, FATS, FATTY SUBSTANCES OR WAXES; FATTY ACIDS THEREFROM; DETERGENTS; CANDLES
- C11D—DETERGENT COMPOSITIONS; USE OF SINGLE SUBSTANCES AS DETERGENTS; SOAP OR SOAP-MAKING; RESIN SOAPS; RECOVERY OF GLYCEROL
- C11D1/00—Detergent compositions based essentially on surface-active compounds; Use of these compounds as a detergent
- C11D1/66—Non-ionic compounds
- C11D1/83—Mixtures of non-ionic with anionic compounds
-
- 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
- C11D10/00—Compositions of detergents, not provided for by one single preceding group
- C11D10/04—Compositions of detergents, not provided for by one single preceding group based on mixtures of surface-active non-soap compounds and soap
- C11D10/045—Compositions of detergents, not provided for by one single preceding group based on mixtures of surface-active non-soap compounds and soap based on non-ionic surface-active compounds and soap
-
- 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
- C11D3/34—Organic compounds containing sulfur
- C11D3/3418—Toluene -, xylene -, cumene -, benzene - or naphthalene sulfonates or sulfates
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- C—CHEMISTRY; METALLURGY
- C11—ANIMAL OR VEGETABLE OILS, FATS, FATTY SUBSTANCES OR WAXES; FATTY ACIDS THEREFROM; DETERGENTS; CANDLES
- C11D—DETERGENT COMPOSITIONS; USE OF SINGLE SUBSTANCES AS DETERGENTS; SOAP OR SOAP-MAKING; RESIN SOAPS; RECOVERY OF GLYCEROL
- C11D3/00—Other compounding ingredients of detergent compositions covered in group C11D1/00
- C11D3/39—Organic or inorganic per-compounds
- C11D3/3947—Liquid 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
- C11D1/02—Anionic compounds
-
- 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
- C11D1/02—Anionic compounds
- C11D1/12—Sulfonic acids or sulfuric acid esters; Salts thereof
- C11D1/22—Sulfonic acids or sulfuric acid esters; Salts thereof derived from aromatic compounds
-
- 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
-
- 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
- C11D1/75—Amino oxides
Definitions
- the invention relates to an aqueous liquid detergent containing builder salts, which contains hydrogen peroxide as a bleaching agent and is distinguished by high storage stability and easy meterability.
- non-aqueous and aqueous liquid detergents containing bleaching per-compounds are known.
- the stabilization of the per-compounds is usually not a problem.
- the stabilization of the anti-segregation agents often presents difficulties.
- sedimentation stabilizers still have to be added.
- Another disadvantage is that often larger amounts of flammable organic solvents have to be added.
- Means of the type mentioned are described for example in DE 12 79 878 (GB 12 05 711), DE 22 33 771 (US 38 50 831), DE 28 25 218 (US 43 16 812) and EP 30 086.
- EP 38 101 proposes encapsulating the bleaching agent granules and suspending them in the agent in this form.
- the alkylbenzenesulfonate is preferably in the form of the sodium salt. Its proportion is preferably 7 to 12% by weight.
- Suitable amine oxides are e.g. B. dodecyldimethylamine oxide, tridecyldimethylamine oxide, tetradecyldimethylamine oxide, pentadecyldimethylamine oxide and hexadecyldimethylamine oxide and mixtures thereof. Their proportion is preferably 2 to 5% by weight.
- Suitable soaps are preferably those from natural fatty acid mixtures, such as coconut or palm kernel fatty acid.
- the fatty acids with 10 and fewer carbon atoms are previously separated off in a proportion of less than 5% by weight, preferably less than 3% by weight (based on soap). It is also advisable to separate the stearic acid to a stearate content below 20% by weight, preferably below 15% by weight (based on soap).
- the proportion of unsaturated fatty acid soaps, such as oleate is advantageously also less than 10%, based on soap.
- the soaps are preferably in the form of sodium salts, the proportion of which is preferably 2 to 5% by weight.
- the proportion of potassium pyrophosphate which is preferably used as tetrapotassium pyrophosphate, is preferably 15 to 21% by weight. Higher proportions, i.e. H. those up to 25% by weight are possible in principle, but are less recommendable for reasons of phosphate restrictions in waste water.
- Suitable hydrotropes are toluenesulfonate, xylene sulfonate and cumene sulfonate, each in the form of the sodium salts. Their proportion is preferably 5 to 10% by weight.
- the hydrogen peroxide is calculated as 100% H2O2. Its proportion is preferably 1 to 4% by weight.
- the water should be deionized and in particular free of heavy metal ions. Its proportion is preferably 50 to 57% by weight. In addition, small amounts of those constituents which are insensitive to oxidation, such as dyes or opacifiers, can be present. Additional stabilizing agents are not required since the agents themselves have a surprisingly high storage stability. After all, small proportions, i.e. H. a maximum of 0.5 to 1% by weight of oxidation-insensitive sequestering stabilizers, such as 1-hydroxyethane-1,1-diphoshonic acid, ethylenediamine-tetra- (methylenephosphonic acid and diethylenetriamine-penta- (methylenephosphonic acid), in each case in the form of Na - or K salt.
- oxidation-insensitive sequestering stabilizers such as 1-hydroxyethane-1,1-diphoshonic acid, ethylenediamine-tetra- (methylenephosphonic acid and diethylenetriamine-penta- (methylenephosphonic acid), in
- the agents are very stable in storage.
- the loss of active oxygen is less than 1% even after storage for several months at room temperature (20 - 25 ° C).
- they are characterized by a high washing and bleaching effect, especially in relation to colored stains.
- a clear, homogeneous, easily pourable liquid detergent had the following composition (in% by weight): 9% C10 ⁇ 13 alkylbenzenesulfonate (Na salt) 3% C13 ⁇ 15 alkyl dimethyl amine oxide 4% coconut soap (Na salt) with 2% C10, 55% C12, 22% C14, 12% C16, 9% C18 20% K4P2O7 8% Na toluenesulfonate 3% H2O2 53% water
- washing tests were carried out in the landerometer.
- a commercial liquid detergent (comparable to an agent according to EP 28 866) containing alkylbenzenesulfonate, nonionic surfactants, coconut soap, enzymes, enzyme stabilizers and water was used.
- the following were used as textile samples: T1 cotton, soiled with dust and skin fat, T2 mixed fabric made of polyester and finished cotton (wash and wear), soiled with dust and skin oil, T3 cotton (refined) soiled with red wine, T4 cotton (refined) soiled with tea stains.
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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)
Abstract
Description
Die Erfindung betrifft ein wäßriges, Buildersalze enthaltendes Flüssigwaschmittel, das Wasserstoffperoxid als bleichendes Agens enthält und sich durch eine hohe Lagerstabilität sowie eine leichte Dosierbarkeit auszeichnet.The invention relates to an aqueous liquid detergent containing builder salts, which contains hydrogen peroxide as a bleaching agent and is distinguished by high storage stability and easy meterability.
Es sind sowohl nichtwäßrige als auch wäßrige Flüssigwaschmittel bekannt, die bleichende Perverbindungen enthalten. In nichtwäßrigen Mitteln ist die Stabilisierung der Perverbindungen meist unproblematisch. Dafür bereitet jedoch die Stabilisierung der Mittel gegen Entmischen vielfach Schwierigkeiten. Man behilft sich meist damit, daß man die Mittel auf eine hohe Viskosität einstellt und die Inhaltsstoffe in einem aufwendigen Mahlprozeß mittels Kolloidmühlen auf eine sehr kleine Korngröße vermahlt. Vielfach müssen noch Sedimentationsstabilisatoren zugesetzt werden. Nachteilig ist ferner, daß vielfach größere Anteile an brennbaren organischen Lösungsmitteln zugesetzt werden müssen. Mittel der genannten Art sind beispielsweise in DE 12 79 878 (GB 12 05 711), DE 22 33 771 (US 38 50 831), DE 28 25 218 (US 43 16 812) und EP 30 086 beschrieben.Both non-aqueous and aqueous liquid detergents containing bleaching per-compounds are known. In non-aqueous agents, the stabilization of the per-compounds is usually not a problem. However, the stabilization of the anti-segregation agents often presents difficulties. One usually helps by adjusting the agents to a high viscosity and grinding the ingredients to a very small grain size in a complex grinding process using colloid mills. In many cases sedimentation stabilizers still have to be added. Another disadvantage is that often larger amounts of flammable organic solvents have to be added. Means of the type mentioned are described for example in DE 12 79 878 (GB 12 05 711), DE 22 33 771 (US 38 50 831), DE 28 25 218 (US 43 16 812) and EP 30 086.
In wäßrigen Flüssigwaschmitteln, in denen die Inhaltsstoffe gelöst sind und daher gegen Phasentrennung im allgemeinen beständiger sind, bereitet die Stabilisierung von sauerstoffhaltigen Bleichmitteln erhebliche Schwierigkeiten. So wird in DE 10 80 722 vorgeschlagen, den Mitteln hochkondensierte Phosphate zuzusetzen und sie auf einen pH-Wert von 6 bis 6,5 einzustellen. Im sauren Bereich ist die Waschkraft jedoch vergleichsweise geringer als im alkalischen. Außerdem sind die Mittel aufgrund ihres hohen Anteils an nichtionischen Tensiden pastös und somit nicht, wie in Verbraucherkreisen bevorzugt, mit Meßbechern dosierbar. Die in DE 15 67 583 (US 36 58 712) beschriebenen Mittel enthalten ein spezielles vernetztes Polymerisat als Stabilisator, das die Mittel ebenfalls sehr dickflüssig und somit schlecht dosierbar macht. In EP 38 101 wird schließlich vorgeschlagen, die Bleichmittelkörner einzukapseln und sie in dieser Form in dem Mittel zu suspendieren. Über die Art des Kapselmaterials, das logischerweise im wäßrigen Vorratskonzentrat beständig bzw. unlöslich, in der wäßrigen Waschlauge hingegen unbeständig bzw. leicht löslich sein muß, finden sich in dem Dokument keine Angaben.In aqueous liquid detergents in which the ingredients are dissolved and are therefore generally more resistant to phase separation, the stabilization of oxygen-containing bleaching agents presents considerable difficulties. So in DE 10 80 722 proposed adding highly condensed phosphates to the compositions and adjusting them to a pH of 6 to 6.5. In the acidic range, however, the washing power is comparatively lower than in the alkaline range. In addition, because of their high proportion of nonionic surfactants, the compositions are pasty and therefore cannot be metered with measuring cups, as is preferred in consumer circles. The agents described in DE 15 67 583 (US 36 58 712) contain a special cross-linked polymer as a stabilizer, which also makes the agents very viscous and therefore difficult to dose. Finally, EP 38 101 proposes encapsulating the bleaching agent granules and suspending them in the agent in this form. There is no information in the document about the nature of the capsule material, which logically has to be stable or insoluble in the aqueous stock concentrate, but has to be inconsistent or easily soluble in the aqueous wash liquor.
Die aufgezeigten Probleme werden durch die vorliegende Erfindung gelöst.The problems outlined are solved by the present invention.
Gegenstand der Erfindung ist ein bleichendes Flüssigwaschmittel enthaltend
- (A) 5 bis 15 Gew.-% eines linearen Alkylbenzolsulfonats mit 9 bis 13 C-Atomen in der Alkylkette in Form des Natrium- oder Kaliumsalzes,
- (B) 1 bis 5 Gew.-% eines Aminoxids, enthaltend einen linearen C₁₂₋₁₆-Alkylrest,
- (C) 1 bis 6 Gew.-% einer von C₁₂₋₁₈-Fettsäuren abgeleiteten Seife in Form des Natrium- oder Kaliumsalzes,
- (D) 10 bis 22 Gew.-% Kaliumpyrophosphat,
- (E) 2 bis 12 Gew.-% eines Hydrotrops,
- (F) 0,5 bis 5 Gew.-% Wasserstoffperoxid,
- (G) 45 bis 60 Gew.-% Wasser.
- (A) 5 to 15% by weight of a linear alkylbenzenesulfonate with 9 to 13 C atoms in the alkyl chain in the form of the sodium or potassium salt,
- (B) 1 to 5% by weight of an amine oxide containing a linear C₁₂₋₁₆ alkyl radical,
- (C) 1 to 6% by weight of a soap derived from C₁₂₋₁₈ fatty acids in the form of the sodium or potassium salt,
- (D) 10 to 22% by weight of potassium pyrophosphate,
- (E) 2 to 12% by weight of a hydrotrope,
- (F) 0.5 to 5% by weight of hydrogen peroxide,
- (G) 45 to 60 wt% water.
Das Alkylbenzolsulfonat liegt vorzugsweise als Natriumsalz vor. Sein Anteil beträgt vorzugsweise 7 bis 12 Gew.-%.The alkylbenzenesulfonate is preferably in the form of the sodium salt. Its proportion is preferably 7 to 12% by weight.
Geeignete Aminoxide sind z. B. Dodecyl-dimethyl-aminoxid, Tridecyl-dimethyl-aminoxid, Tetradecyl-dimethyl-aminoxid, Pentadecyl-dimethyl-aminoxid und Hexadecyl-dimethyl-aminoxid sowie deren Gemische. Vorzugsweise beträgt ihr Anteil 2 bis 5 Gew.-%.Suitable amine oxides are e.g. B. dodecyldimethylamine oxide, tridecyldimethylamine oxide, tetradecyldimethylamine oxide, pentadecyldimethylamine oxide and hexadecyldimethylamine oxide and mixtures thereof. Their proportion is preferably 2 to 5% by weight.
Als Seifen eignen sich vorzugsweise solche aus natürlichen Fettsäuregemischen, wie Cocos- oder Palmkernfettsäure. Die Fettsäuren mit 10 und weniger C-Atomen werden zuvor auf einen Anteil von weniger als 5 Gew.-%, vorzugsweise auf weniger als 3 Gew.-% (bezogen auf Seife) abgetrennt. Ebenso empfiehlt es sich, die Stearinsäure auf einen Stearatgehalt unter 20 Gew.-%, vorzugsweise unter 15 Gew.-% (bezogen auf Seife) abzutrennen. Der Anteil an ungesättigten fettsauren Seifen, wie Oleat, beträgt zweckmäßigerweise ebenfalls unter 10 %, bezogen auf Seife. Die Seifen liegen bevorzugt als Natriumsalze vor, wobei deren Anteil bevorzugt 2 bis 5 Gew.-% beträgt.Suitable soaps are preferably those from natural fatty acid mixtures, such as coconut or palm kernel fatty acid. The fatty acids with 10 and fewer carbon atoms are previously separated off in a proportion of less than 5% by weight, preferably less than 3% by weight (based on soap). It is also advisable to separate the stearic acid to a stearate content below 20% by weight, preferably below 15% by weight (based on soap). The proportion of unsaturated fatty acid soaps, such as oleate, is advantageously also less than 10%, based on soap. The soaps are preferably in the form of sodium salts, the proportion of which is preferably 2 to 5% by weight.
Der Anteil des Kaliumpyrophosphats, das bevorzugt als Tetrakaliumpyrophosphat eingesetzt wird, beträgt vorzugsweise 15 bis 21 Gew.-%. Höhere Anteile, d. h. solche bis 25 Gew.-%, sind zwar grundsätzlich möglich, aus Gründen der Phosphatbeschränkungen im Abwasser jedoch weniger empfehlenswert.The proportion of potassium pyrophosphate, which is preferably used as tetrapotassium pyrophosphate, is preferably 15 to 21% by weight. Higher proportions, i.e. H. those up to 25% by weight are possible in principle, but are less recommendable for reasons of phosphate restrictions in waste water.
Als Hydrotrop eignen sich Toluolsulfonat, Xylolsulfonat und Cumolsulfonat, jeweils in Form der Natriumsalze. Vorzugsweise beträgt ihr Anteil 5 bis 10 Gew.-%.Suitable hydrotropes are toluenesulfonate, xylene sulfonate and cumene sulfonate, each in the form of the sodium salts. Their proportion is preferably 5 to 10% by weight.
Das Wasserstoffperoxid ist als 100%iges H₂O₂ berechnet. Sein Anteil beträgt vorzugsweise 1 bis 4 Gew.-%.The hydrogen peroxide is calculated as 100% H₂O₂. Its proportion is preferably 1 to 4% by weight.
Das Wasser soll entionisiert und insbesondere frei von Schwermetallionen sein. Sein Anteil beträgt vorzugsweise 50 bis 57 Gew.-%. Zusätzlich können in geringer Menge solche Bestandteile anwesend sein, die gegen Oxidation unempfindlich sind, wie Farbstoffe oder Trübungsmittel. Zusätzliche Stabilisierungsmittel sind nicht erforderlich, da die Mittel bereits von sich aus eine überraschend hohe Lagerstabilität aufweisen. Immerhin können geringe Anteile, d. h. maximal 0,5 bis 1 Gew.-%, an oxidationsunempfindlichen sequestrierend wirkenden Stabilisatoren anwesend sein, wie 1-Hydroxyethan-1,1-diphoshponsäure, Ethylendiamin-tetra-(methylenphosphonsäure und Diethylentriamin-penta-(methylenphosphonsäure), jeweils in Form des Na- oder K-Salzes.The water should be deionized and in particular free of heavy metal ions. Its proportion is preferably 50 to 57% by weight. In addition, small amounts of those constituents which are insensitive to oxidation, such as dyes or opacifiers, can be present. Additional stabilizing agents are not required since the agents themselves have a surprisingly high storage stability. After all, small proportions, i.e. H. a maximum of 0.5 to 1% by weight of oxidation-insensitive sequestering stabilizers, such as 1-hydroxyethane-1,1-diphoshonic acid, ethylenediamine-tetra- (methylenephosphonic acid and diethylenetriamine-penta- (methylenephosphonic acid), in each case in the form of Na - or K salt.
Die Mittel sind ungeachtet ihrer alkalischen Reaktion sehr lagerstabil. Der Verlust an Aktivsauerstoff beträgt auch nach mehrmonatiger Lagerung bei Raumtemperatur (20 - 25 °C) weniger als 1 %. Bei der Anwendung zeichnen sie sich durch eine hohe Wasch- und Bleichwirkung insbesondere gegenüber farbigen Anschmutzungen aus.Regardless of their alkaline reaction, the agents are very stable in storage. The loss of active oxygen is less than 1% even after storage for several months at room temperature (20 - 25 ° C). When used, they are characterized by a high washing and bleaching effect, especially in relation to colored stains.
Ein klares, homogenes, leicht gießbares Flüssigwaschmittel wies die folgende Zusammensetzung auf (in Gew.-%):
9 % C₁₀₋₁₃-Alkylbenzolsulfonat (Na-Salz)
3 % C₁₃₋₁₅-Alkyl-dimethyl-aminoxid
4 % Cocosseife (Na-Salz) mit 2 % C₁₀, 55 % C₁₂, 22 % C₁₄, 12 % C₁₆, 9 % C₁₈
20 % K₄P₂O₇
8 % Na-Toluolsulfonat
3 % H₂O₂
53 % WasserA clear, homogeneous, easily pourable liquid detergent had the following composition (in% by weight):
9% C₁₀₋₁₃ alkylbenzenesulfonate (Na salt)
3% C₁₃₋₁₅ alkyl dimethyl amine oxide
4% coconut soap (Na salt) with 2% C₁₀, 55% C₁₂, 22% C₁₄, 12% C₁₆, 9% C₁₈
20% K₄P₂O₇
8% Na toluenesulfonate
3% H₂O₂
53% water
Bei einer Lagerung in verschlossenen Kunststoffflaschen bei 25 °C betrug der Aktivsauerstoff-Gehalt nach 2 Monaten noch 100 % und nach 4 Monaten noch 98 % des Ausgangswertes. Nach 15 Monaten betrug der Erhaltungsgrad 40 %.When stored in sealed plastic bottles at 25 ° C, the active oxygen content was still 100% after 2 months and 98% after 4 months. After 15 months, the degree of conservation was 40%.
Zur Prüfung des Wasch- und Bleichvermögens wurden Waschversuche im Landerometer durchgeführt. Zum Vergleich wurde ein Flüssigwaschmittel des Handels (vergleichbar einem Mittel gemäß EP 28 866) mit einem Gehalt an Alkylbenzolsulfonat, nichtionischen Tensiden, Cocosseife, Enzymen, Enzymstabilisatoren und Wasser verwendet. Als Textilproben dienten:
T1 Baumwolle, angeschmutzt mit Staub und Hautfett,
T2 Mischgewebe aus Polyester und veredelter Baumwolle (wash and wear), angeschmutzt mit Staub und Hautfett,
T3 Baumwolle (veredelt) angeschmutzt mit Rotwein,
T4 Baumwolle (veredelt) angeschmutzt mit Teeflecken.To test the washing and bleaching ability, washing tests were carried out in the landerometer. For comparison, a commercial liquid detergent (comparable to an agent according to EP 28 866) containing alkylbenzenesulfonate, nonionic surfactants, coconut soap, enzymes, enzyme stabilizers and water was used. The following were used as textile samples:
T1 cotton, soiled with dust and skin fat,
T2 mixed fabric made of polyester and finished cotton (wash and wear), soiled with dust and skin oil,
T3 cotton (refined) soiled with red wine,
T4 cotton (refined) soiled with tea stains.
Wasserhärte 16 °d (160 mg CaO pro Liter), Konzentration 6,5 g/l, 15 Minuten bei 60 °C, 3maliges Nachspülen, photometrische Ausmessung, Mittelwert aus 3 Bestimmungen.Water hardness 16 ° d (160 mg CaO per liter), concentration 6.5 g / l, 15 minutes at 60 ° C, 3 rinses, photometric measurement, average of 3 determinations.
Die Ergebnisse sind in der folgenden Tabelle zusammengestellt. Sie zeigen die Überlegenheit des Mittels sowohl gegenüber fettigmineralischen Anschmutzungen als auch gegenüber bleichbaren Flecken.
Claims (8)
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
DE19893906044 DE3906044A1 (en) | 1989-02-27 | 1989-02-27 | BLEACHING LIQUID DETERGENT |
DE3906044 | 1989-02-27 |
Publications (1)
Publication Number | Publication Date |
---|---|
EP0385216A1 true EP0385216A1 (en) | 1990-09-05 |
Family
ID=6375014
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
EP90103139A Withdrawn EP0385216A1 (en) | 1989-02-27 | 1990-02-19 | Bleaching liquid detergents |
Country Status (4)
Country | Link |
---|---|
EP (1) | EP0385216A1 (en) |
DE (1) | DE3906044A1 (en) |
PT (1) | PT93238A (en) |
WO (1) | WO1990010055A1 (en) |
Cited By (9)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
WO1996030485A1 (en) * | 1995-03-24 | 1996-10-03 | Warwick International Group Limited | Alkaline isotropic liquid detergent with peroxide |
WO1996030486A1 (en) * | 1995-03-24 | 1996-10-03 | Warwick International Group Limited | Alkaline isotropic liquid detergent with peroxide |
WO1996030483A1 (en) * | 1995-03-24 | 1996-10-03 | Warwick International Group Limited | Alkaline isotropic liquid detergent with peroxide |
WO1996030484A1 (en) * | 1995-03-24 | 1996-10-03 | Warwick International Group Limited | Alkaline isotropic liquid detergent with peroxide |
EP0779357A1 (en) * | 1995-12-16 | 1997-06-18 | The Procter & Gamble Company | Stable emulsions comprising a hydrophobic liquid ingredient |
EP0962520A1 (en) * | 1998-05-29 | 1999-12-08 | The Procter & Gamble Company | Liquid bleaching compositions |
GB2339789A (en) * | 1998-07-16 | 2000-02-09 | Reckitt & Colman Inc | Aqueous cleaning and surface treatment compositions |
WO2000023555A1 (en) * | 1998-10-22 | 2000-04-27 | Colgate-Palmolive Company | Thickened liquid hydrogen peroxide bleach compositions |
EP1065262A1 (en) * | 1999-06-29 | 2001-01-03 | The Procter & Gamble Company | Bleaching compositions |
Families Citing this family (16)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
FR2766724B1 (en) * | 1997-07-31 | 1999-10-22 | Irdec Sa | NON-AGGRESSIVE DECONTAMINANT COMPOSITIONS |
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DE3519689A1 (en) * | 1985-06-01 | 1986-12-04 | Henkel KGaA, 4000 Düsseldorf | Liquid detergent concentrate |
-
1989
- 1989-02-27 DE DE19893906044 patent/DE3906044A1/en not_active Withdrawn
-
1990
- 1990-02-19 EP EP90103139A patent/EP0385216A1/en not_active Withdrawn
- 1990-02-19 WO PCT/EP1990/000269 patent/WO1990010055A1/en unknown
- 1990-02-22 PT PT9323890A patent/PT93238A/en not_active Application Discontinuation
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BE657865A (en) * | 1964-01-04 | 1965-07-05 | ||
US4298492A (en) * | 1979-06-21 | 1981-11-03 | Lever Brothers Company | Built liquid detergent composition |
DE3519689A1 (en) * | 1985-06-01 | 1986-12-04 | Henkel KGaA, 4000 Düsseldorf | Liquid detergent concentrate |
Cited By (15)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
WO1996030485A1 (en) * | 1995-03-24 | 1996-10-03 | Warwick International Group Limited | Alkaline isotropic liquid detergent with peroxide |
WO1996030486A1 (en) * | 1995-03-24 | 1996-10-03 | Warwick International Group Limited | Alkaline isotropic liquid detergent with peroxide |
WO1996030483A1 (en) * | 1995-03-24 | 1996-10-03 | Warwick International Group Limited | Alkaline isotropic liquid detergent with peroxide |
WO1996030484A1 (en) * | 1995-03-24 | 1996-10-03 | Warwick International Group Limited | Alkaline isotropic liquid detergent with peroxide |
EP0910465A1 (en) * | 1995-12-16 | 1999-04-28 | The Procter & Gamble Company | Stable emulsions comprising a hydrophobic liquid ingredient |
EP0910465A4 (en) * | 1995-12-16 | 1999-04-28 | ||
EP0779357A1 (en) * | 1995-12-16 | 1997-06-18 | The Procter & Gamble Company | Stable emulsions comprising a hydrophobic liquid ingredient |
EP0962520A1 (en) * | 1998-05-29 | 1999-12-08 | The Procter & Gamble Company | Liquid bleaching compositions |
WO1999063033A1 (en) * | 1998-05-29 | 1999-12-09 | The Procter & Gamble Company | Liquid bleaching compositions |
US6482786B1 (en) | 1998-05-29 | 2002-11-19 | The Procter & Gamble Company | Liquid bleaching compositions comprising hydrogen peroxide, betaine, and ethoxylated nonionic surfactant |
GB2339789A (en) * | 1998-07-16 | 2000-02-09 | Reckitt & Colman Inc | Aqueous cleaning and surface treatment compositions |
US6531437B1 (en) | 1998-07-16 | 2003-03-11 | Reckitt Benckiser Inc | Shelf stable, aqueous hydrogen peroxide containing carpet cleaning and treatment compositions |
WO2000023555A1 (en) * | 1998-10-22 | 2000-04-27 | Colgate-Palmolive Company | Thickened liquid hydrogen peroxide bleach compositions |
EP1065262A1 (en) * | 1999-06-29 | 2001-01-03 | The Procter & Gamble Company | Bleaching compositions |
WO2001000774A1 (en) * | 1999-06-29 | 2001-01-04 | The Procter & Gamble Company | Bleaching compositions |
Also Published As
Publication number | Publication date |
---|---|
WO1990010055A1 (en) | 1990-09-07 |
DE3906044A1 (en) | 1990-08-30 |
PT93238A (en) | 1990-08-31 |
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