EP0036625B1 - Liquid cleaning agents - Google Patents
Liquid cleaning agents Download PDFInfo
- Publication number
- EP0036625B1 EP0036625B1 EP81102003A EP81102003A EP0036625B1 EP 0036625 B1 EP0036625 B1 EP 0036625B1 EP 81102003 A EP81102003 A EP 81102003A EP 81102003 A EP81102003 A EP 81102003A EP 0036625 B1 EP0036625 B1 EP 0036625B1
- Authority
- EP
- European Patent Office
- Prior art keywords
- weight
- alkanol
- optionally
- cleaner
- ethylene oxide
- 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.)
- Expired
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
- C11D1/00—Detergent compositions based essentially on surface-active compounds; Use of these compounds as a detergent
- C11D1/88—Ampholytes; Electroneutral compounds
- C11D1/94—Mixtures with anionic, cationic or 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
- C11D1/02—Anionic compounds
- C11D1/12—Sulfonic acids or sulfuric acid esters; Salts thereof
- C11D1/14—Sulfonic acids or sulfuric acid esters; Salts thereof derived from aliphatic hydrocarbons or mono-alcohols
- C11D1/143—Sulfonic acid esters
-
- 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
- C11D1/02—Anionic compounds
- C11D1/12—Sulfonic acids or sulfuric acid esters; Salts thereof
- C11D1/29—Sulfates of polyoxyalkylene ethers
-
- 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
- C11D1/72—Ethers of polyoxyalkylene glycols
-
- 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
- C11D1/88—Ampholytes; Electroneutral compounds
- C11D1/90—Betaines
Definitions
- Liquid washing, rinsing and cleaning agents are usually aqueous solutions of anionic and / or nonionic surfactants and customary additives. They are used for washing textiles, for cleaning hard surfaces, for example glasses or ceramic materials, plastics, lacquered and. polished surfaces, which can also be metallic in nature, are used. A preferred area of application for such agents is the manual washing of dining utensils and other related equipment. The respective cleaning processes are usually carried out at slightly elevated temperatures. There is always an increased impact on human skin.
- the present invention therefore relates to cleaning agents with improved skin protection and strong washing power.
- alkyl ether sulfates that is to say sulfated adducts of about 2 to 5 moles of ethylene oxide with fatty alcohols with about 10 to 16 carbon atoms in the alkyl radical, have good washing power and at the same time have a mild effect on the skin.
- the commercially available dishwashing agents which are to be used manually are therefore aqueous solutions of such alkyl ether sulfates in combination with other anionic surfactants such as n-alkylbenzenesulfonates and / or alkanesulfonates, optionally also olefin sulfonates or alkyl sulfates and nonionic surfactants, solubilizers, colorants and fragrances.
- alkyl ether sulfate mixture consisting of 50 percent by weight of a C 12 alkyl ether sulfate and 50 percent by weight of a C 4 alkyl ether sulfate with 1 to 5, preferably 2 to 4, ethylene oxide groups as ether component compared to the alkyl ether sulfate mixture normally used, that contains the same components in a weight ratio of 70:30 leads to an unexpected further reduction in skin irritation without reducing the known good washing power of such agents. Small additional amounts of alkyl ether sulfates with more or less than 12 or 14 carbon atoms in the alkyl radical change these good results only insignificantly, but should be avoided if possible.
- betaine-type amphoteric surfactants have a mild effect on the skin. It was therefore expected that a combination of the mixture of C 12 / C 14 alkyl ether sulfates and betaines used according to the invention would show an additional increase in skin tolerance. However, this expected effect could not be determined. It was all the more surprising, however, that a significant increase in washing effectiveness could be achieved by further addition of such betaines.
- the present invention therefore relates to a liquid cleaning agent based on an aqueous solution of anionic surfactants, optionally together with nonionic surfactants, solvents, solubilizers, corrosion inhibitors, preservatives, thickeners and colorants and fragrances, which is characterized in that it is 2 to 40 percent by weight a mixture of 50 parts by weight of a sulfated adduct of 1 to 5 ethylene oxide with an nC 12 alkanol and with an nC 14 alkanol and optionally up to 20 percent by weight of a surface-active betaine.
- a preferred embodiment of the liquid cleaning agent according to the invention is characterized in that it contains 4 to 20 percent by weight of a mixture of 50 parts by weight of a sulfated adduct of 2 to 4 moles of ethylene oxide with an nC 12 alkanol and with an nC 14 alkanol and optionally 2 to 5 Contains percent by weight of a surfactant betaine.
- composition of the aqueous cleaning agent solution according to the invention is as follows:
- composition of the aqueous cleaning agent solution according to the invention is preferred:
- alkyl ether sulfates with different chain lengths of the alkyl radicals or higher degrees of ethoxylation from those of the compounds according to the invention can be used as anionic surfactants.
- anionic surfactants which can be used include n-alkylbenzenesulfonates with 9 to 16, preferably 12 carbon atoms in the alkyl radical, alkanesulfonates with 10 to 20, preferably 12 to 18 carbon atoms in the alkyl radical, olefin sulfonates with 12 to 16, preferably 12 to 14, carbon atoms in the n- Alkyl radical and alkyl sulfates having 8 to 18, preferably 8 to 14 carbon atoms in the alkyl radical.
- R 1 is an alkyl radical with 8 to 20, preferably 10 to 18 carbon atoms and R 2 and R 3 , which may be interrupted by heteroatoms or heteroatom groups, and R 2 and R 3 are identical or different alkyl radicals having 1 to 3 carbon atoms.
- R 1 is an alkyl radical with 8 to 20, preferably 10 to 18 carbon atoms and R 2 and R 3 , which may be interrupted by heteroatoms or heteroatom groups, and R 2 and R 3 are identical or different alkyl radicals having 1 to 3 carbon atoms.
- C 10 -C 18 -Alkyl-dimethylcarboxymethylbetaine and C 11 -C 17 -Alkylamidopropyl-dimethylcarboxymethylbetaine are preferred.
- the solvents to be added if necessary are low molecular weight alkanols with 1 to 4 carbon atoms in the molecule, preferably ethanol and isapropanol.
- Solubilizers for example for dyes and perfume oils, can be used, for example, as alkanolamines, polyols such as ethylene glycol, 1,2-propylene glycol, glycerol and alkylbenzenesulfionates with 1 to 3 carbon atoms in the alkyl radical.
- the preferred thickeners include urea, sodium chloride, ammonium chloride and magnesium chloride, which can also be used in combination.
- corrosion inhibitors and preservatives are sodium benzoate, formaldehyde and sodium sulfite.
- liquid cleaning agents according to the invention can also contain conventional disinfectants, since they have no effect on the skin-protecting effect of the alkyl ether sulfate mixture used in accordance with the invention.
- liquid cleaning agents according to the invention of the following examples were obtained by stirring the individual components together in any order and leaving the mixture to stand until there were no bubbles.
- the sodium salts were used as anionic surfactants.
- EO means ethylene oxide.
- Examples 1 to 6 were used for comparative experiments.
- the sulfate mixture according to the invention was replaced in each case in equal quantities by a 70:30 C 12 - / C 14 alkyl (EO) 2 sulfate mixture.
- the betaine was omitted and the surfactant proportions increased proportionately.
- the comparison products correspond to commercially available cleaning agents. In all cases, skin irritation was determined according to the soap-chamber test (cf. "Journal of the American Academy of Dermatology" 1 [1979], pages 35 to 41).
- the so-called plate test was also carried out.
- the methodology is in the magazine »Fette; Soap; Anstrichsch «, 74 [1972], pages 163 to 165. It was mainly used with water of 45 ° C / 16 ° d and the use of 0.5 g / I product as well as a mixed contamination from protein, fat and carbohydrates.
- the mixed soiling was used with 2 g / plate (saucer 14 cm in diameter; distributed in the cup recess); the soiled plates were rinsed after 15 hours of storage at ⁇ 0 to + 5 ° C under the conditions specified above.
Landscapes
- 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)
- Lubricants (AREA)
- Cleaning By Liquid Or Steam (AREA)
- Fluid-Pressure Circuits (AREA)
Abstract
Description
Flüssige Wasch-, Spül- und Reinigungsmittel stellen meist wäßrige Lösungen von anionischen und/oder nichtionischen Tensiden und üblichen Zusatzstoffen dar. Sie werden zum Waschen von Textilien, zum Reinigen harter Oberflächen, zum Beispiel von Gläsern oder keramischen Materialien, von Kunststoffen, lackierten und. polierten Oberflächen, die auch metallischer Natur sein können, vewendet. Ein bevorzugtes Anwendungsgebiet derartiger Mittel ist das manuelle Spülen von Eßgeschirr und anderen damit verwandten Gerätschaften. Die jeweiligen Reinigungsvorgänge werden üblicherweise bei leicht erhöhten Temperaturen durchgeführt. Dabei findet stets eine verstärkte Einwirkung auf die menschliche Haut statt.Liquid washing, rinsing and cleaning agents are usually aqueous solutions of anionic and / or nonionic surfactants and customary additives. They are used for washing textiles, for cleaning hard surfaces, for example glasses or ceramic materials, plastics, lacquered and. polished surfaces, which can also be metallic in nature, are used. A preferred area of application for such agents is the manual washing of dining utensils and other related equipment. The respective cleaning processes are usually carried out at slightly elevated temperatures. There is always an increased impact on human skin.
Die vorliegende Erfindung betrifft daher Reinigungsmittel mit verbesserter Hautschutzwirkung und starker Waschkraft.The present invention therefore relates to cleaning agents with improved skin protection and strong washing power.
Es ist bekannt, daß sogenannte Alkylethersulfate, das heißt sulfatierte Anlagerungsprodukte von etwa 2 bis 5 Mol Ethylenoxid an Fettalkohole mit etwa 10 bis 16 Kohlenstoffatomen im Alkylrest eine gute Waschkraft bei gleichzeitiger milder Wirkung auf die Haut besitzen. Die marktüblichen, manuell anzuwendenden Geschirrspülmittel stellen daher wäßrige Lösungen solcher Alkylethersulfate in Verbindung mit anderen anionischen Tensiden wie n-Alkylbenzolsulfonaten und/oder Alkansulfonaten, gegebenenfalls auch Olefinsulfonaten oder Alkylsulfaten sowie-nichtionischen Tensiden, Lösungsvermittlern, Farb- und Duftstoffen dar.It is known that so-called alkyl ether sulfates, that is to say sulfated adducts of about 2 to 5 moles of ethylene oxide with fatty alcohols with about 10 to 16 carbon atoms in the alkyl radical, have good washing power and at the same time have a mild effect on the skin. The commercially available dishwashing agents which are to be used manually are therefore aqueous solutions of such alkyl ether sulfates in combination with other anionic surfactants such as n-alkylbenzenesulfonates and / or alkanesulfonates, optionally also olefin sulfonates or alkyl sulfates and nonionic surfactants, solubilizers, colorants and fragrances.
Es wurde nun überraschend gefunden, daß der Einsatz eines Alkylethersulfatgemisches, bestehend aus 50 Gewichtsprozent eines C12-Alkylethersulfats und 50 Gewichtsprozent eines C,4-Alkylether- sulfats mit 1 bis 5, vorzugsweise 2 bis 4 Ethylenoxidgruppen als Etherkomponente gegenüber dem üblicherweise eingesetzten Alkylethersulfatgemisch, das die gleichen Komponenten im Gewichtsverhältnis 70 : 30 enthält, zu einer unerwarteten weiteren Verminderung der Hautirritätion führt, ohne die bekannt gute Waschkraft derartiger Mittel zu mindern. Geringfügige zusätzliche Mengen an Alkylethersulfaten mit mehr oder weniger als 12 beziehungsweise 14 Kohlenstoffatomen im Alkylrest verändern diese guten Ergebnisse nur unwesentlich, sollten jedoch möglichst vermieden werden.It has now surprisingly been found that the use of an alkyl ether sulfate mixture consisting of 50 percent by weight of a C 12 alkyl ether sulfate and 50 percent by weight of a C 4 alkyl ether sulfate with 1 to 5, preferably 2 to 4, ethylene oxide groups as ether component compared to the alkyl ether sulfate mixture normally used, that contains the same components in a weight ratio of 70:30 leads to an unexpected further reduction in skin irritation without reducing the known good washing power of such agents. Small additional amounts of alkyl ether sulfates with more or less than 12 or 14 carbon atoms in the alkyl radical change these good results only insignificantly, but should be avoided if possible.
Es ist weiterhin bekannt, daß amphotere oberflächenaktive Mittel vom Betaintyp eine milde Wirkung auf die Haut ausüben. Daher wurde erwartet, daß eine Kombination der erfindungsgemäß eingesetzten Mischung aus C12/C14-Alkylethersulfaten mit Betainen eine zusätzliche Steigerung der Hautverträglichkeit zeigen würde. Diese erwartete Wirkung konnte jedoch nicht ermittelt werden. Um so überraschender war jedoch, daß durch weiteren Zusatz derartiger Betaine eine signifikante Steigerung der Waschwirksamkeit erzielt werden konnte.It is also known that betaine-type amphoteric surfactants have a mild effect on the skin. It was therefore expected that a combination of the mixture of C 12 / C 14 alkyl ether sulfates and betaines used according to the invention would show an additional increase in skin tolerance. However, this expected effect could not be determined. It was all the more surprising, however, that a significant increase in washing effectiveness could be achieved by further addition of such betaines.
Gegenstand der vorliegenden Erfindung ist daher ein flüssiges Reinigungsmittel auf Basis einer wäßrigen Lösung von anionischen Tensiden, gegebenenfalls zusammen mit nichtionischen Tensiden, Lösungsmitteln, Lösungsvermittlern, Korrosionsinhibitoren, Konservierungsmitteln, Verdickungsmitteln sowie Farb- und Duftstoffen, das dadurch gekennzeichnet ist, daß es 2 bis 40 Gewichtsprozent eines Gemisches aus je 50 Gewichtsteilen eines sulfatierten Anlagerungsproduktes von 1 bis 5 Ethylenoxid an ein n-C12-Alkanol und an ein n-C14-Alkanol und gegebenenfalls bis zu 20 Gewichtsprozent eines oberflächenaktiven Betains enthält.The present invention therefore relates to a liquid cleaning agent based on an aqueous solution of anionic surfactants, optionally together with nonionic surfactants, solvents, solubilizers, corrosion inhibitors, preservatives, thickeners and colorants and fragrances, which is characterized in that it is 2 to 40 percent by weight a mixture of 50 parts by weight of a sulfated adduct of 1 to 5 ethylene oxide with an nC 12 alkanol and with an nC 14 alkanol and optionally up to 20 percent by weight of a surface-active betaine.
Eine bevorzugte Ausführungsform des erfindungsgemäßen flüssigen Reinigungsmittels ist dadurch gekennzeichnet, daß es 4 bis 20 Gewichtsprozent eines Gemisches aus je 50 Gewichtsteilen eines sulfatierten Anlagerungsproduktes von 2 bis 4 Mol Ethylenoxid an ein n-C12-Alkanol und an ein n-C14-Alkanol und gegebenenfalls 2 bis 5 Gewichtsprozent eines oberflächenaktiven Betains enthält.A preferred embodiment of the liquid cleaning agent according to the invention is characterized in that it contains 4 to 20 percent by weight of a mixture of 50 parts by weight of a sulfated adduct of 2 to 4 moles of ethylene oxide with an nC 12 alkanol and with an nC 14 alkanol and optionally 2 to 5 Contains percent by weight of a surfactant betaine.
Die Zusammensetzung der erfindungsgemäßen wäßrigen Reinigungsmittellösung bewegt sich in folgendem Rahmen:
, Folgende Zusammensetzung der erfindungsgemäßen wäßrigen Reinigungsmittellösung wird bevorzugt:
Die erfindungsgemäß eingesetzten Alkylethersulfate entsprechen der Formel
Weitere Alkylethersulfate mit von denen der erfindungsgemäßen Verbindungen abweichenden Kettenlängen der Alkylreste oder höheren Ethoxylierungsgraden können als anionische Tenside eingesetzt werden. Darüber hinaus gehören zu den einsetzbaren anionischen Tensiden n-Alkylbenzolsulfonate mit 9 bis 16, vorzugsweise 12 Kohlenstoffatomen im Alkylrest, Alkansulfonate mit 10 bis 20, vorzugsweise 12 bis 18 Kohlenstoffatomen im Alkylrest, Olefinsulfonate mit 12 bis 16, vorzugsweise 12 bis 14 Kohlenstoffatomen im n-Alkylrest und Alkylsulaten mit 8 bis 18, vorzugsweise 8 bis 14 Kohlenstoffatomen im Alkylrest.Further alkyl ether sulfates with different chain lengths of the alkyl radicals or higher degrees of ethoxylation from those of the compounds according to the invention can be used as anionic surfactants. In addition, the anionic surfactants which can be used include n-alkylbenzenesulfonates with 9 to 16, preferably 12 carbon atoms in the alkyl radical, alkanesulfonates with 10 to 20, preferably 12 to 18 carbon atoms in the alkyl radical, olefin sulfonates with 12 to 16, preferably 12 to 14, carbon atoms in the n- Alkyl radical and alkyl sulfates having 8 to 18, preferably 8 to 14 carbon atoms in the alkyl radical.
Als amphotere oberflächenaktive Betaine werden Verbindungen der Formel
Sofern nichtionische Tenside eingesetzt werden, sind Anlagerungsprodukte von 4 bis 20, vorzugs= weise 6 bis 15 Mol Alkylenoxid, vorzugsweise Ethylenoxid an C8―C12-Alkylbenzole, C10―C20-, vorzugsweisse C12―C18-Alkanole, C10―C18-,Carbonsäurealkanolamide, aber auch die Anlagerungsprodukte von Ethylenoxid an Polypropylenglykole, die unter dem Namen Pluronics® bekanntgeworden sind, sowie Anlagerungsprodukte von 1 bis 7 Mol Ethylenoxid an mit 1 bis 5 Mol Propylenoxid umgesetzte C12―C18-Alkanole geeignet.If nonionic surfactants are used, adducts of 4 to 20, preferably = 6 to 15, mol of alkylene oxide, preferably ethylene oxide over C 8 -C 12 alkylbenzenes, C 10 -C 20 -, preferably white C 12 -C 18 alkanols, C 10 -C 18 -, Carbonsäurealkanolamide, but also the addition products of ethylene oxide with polypropylene glycols which have become known under the names Pluronics ®, as well as addition products of 1 to 7 moles of ethylene oxide with 1 to 5 moles of propylene oxide unreacted C 12 -C 18 alkanols suitable .
Bei den bei Bedarf zuzusetzenden Lösungsmitteln handelt es sich um niedermolekulare Alkanole mit 1 bis 4 Kohlenstoffatomen im Molekül, vorzugsweise um Ethanol und Isapropanol.The solvents to be added if necessary are low molecular weight alkanols with 1 to 4 carbon atoms in the molecule, preferably ethanol and isapropanol.
Als Lösungsvermittler, etwa für Farbstoffe und Parfümöle können beispielsweise Alkanolamine, Polyole wie Ethylenglykol, Propylenglykol-1,2, Glycerin sowie Alkylbenzolsulfionate mit 1 bis 3Kohlenstoffatomen im Alkylrest dienen.Solubilizers, for example for dyes and perfume oils, can be used, for example, as alkanolamines, polyols such as ethylene glycol, 1,2-propylene glycol, glycerol and alkylbenzenesulfionates with 1 to 3 carbon atoms in the alkyl radical.
Zu den bevorzugten Verdickungsmitteln zählen Harnstoff, Natriumchlorid, Ammoniumchlorid und Magnesiumchlorid, die auch kombiniert eingesetzt werden können. Als Korrosionsinhibitoren und Konservierungsmittel sind beispielsweise Natriumbenzoat, Formatdehyd und Natriumsulfit zu nennen.The preferred thickeners include urea, sodium chloride, ammonium chloride and magnesium chloride, which can also be used in combination. Examples of corrosion inhibitors and preservatives are sodium benzoate, formaldehyde and sodium sulfite.
Die erfindungsgemäßen flüssigen Reinigungsmittel-können auch übliche-Desinfektionsmittel enthalten, da sie keine Auswirkung auf die hautschützende Wiekung des erfirtdüngsgemäß eingesetzten Alkylethersulfat-Gemisches haben.The liquid cleaning agents according to the invention can also contain conventional disinfectants, since they have no effect on the skin-protecting effect of the alkyl ether sulfate mixture used in accordance with the invention.
Die erfindungsgemäßen flüssigen Reinigungsmittel der folgenden Beispiele wurden durch Zusammenrühren der einzelnen Bestandteile in beliebiger Reihenfolge und Stehenlassen des Gemisches bis zur Blasenfreiheit erhalten. Es wurden jeweils die Natriumsalze als anionische Tenside eingesetzt. EO bedeutet Ethylenoxid.The liquid cleaning agents according to the invention of the following examples were obtained by stirring the individual components together in any order and leaving the mixture to stand until there were no bubbles. The sodium salts were used as anionic surfactants. EO means ethylene oxide.
Die Beispiele 1 bis 6 wurden für Vergleichsversuche herangezogen. Dabei wurde bei den Beispielen 1 bis 3 das erfindungsgemäße Sulfatgemisch jeweils mengengleich durch ein 70 : 30-C12-/C14-Alkyl-(EO)2-sulfatgemisch ersetzt. Bei den Beispielen 4 bis 6 wurde das Betain weggelassen und die Tensidanteile verhältnisgleich erhöht. Die Vergleichsprodukte entsprechen handelsüblichen Reinigungsmitteln. In allen Fällen wurde die Hautirritation nach dem Seifen-Kammer-Test (vgl. »Journal of the American Academy of Dermatology« 1 [1979], Seiten 35 bis 41) bestimmt.Examples 1 to 6 were used for comparative experiments. In Examples 1 to 3, the sulfate mixture according to the invention was replaced in each case in equal quantities by a 70:30 C 12 - / C 14 alkyl (EO) 2 sulfate mixture. In Examples 4 to 6, the betaine was omitted and the surfactant proportions increased proportionately. The comparison products correspond to commercially available cleaning agents. In all cases, skin irritation was determined according to the soap-chamber test (cf. "Journal of the American Academy of Dermatology" 1 [1979], pages 35 to 41).
Außerdem wurde der sognannte Tellertest durchgeführt. Die Methodik ist in der Zeitschrift »Fette; Seifen; Anstrichmittel«, 74 [1972], Seiten 163 bis 165 beschrieben. Es wurde vorwiegend mit Wasser von 45°C/16°d und einem Einsatz von 0,5 g/I Produkt sowie einer Mischanschmutzung aus Eiweiß, Fett und Kohlehydraten gearbeitet. Die Mischanschmutzung wurde mit 2 g/Teller (Untertasse von 14 cm Durchmesser; verteilt in der Tassenvertiefung) eingesetzt; die angeschmutzten Teller wurden nach 15 Stunden Lagerung bei ±0 bis +5°C unter den oben angegebenen Bedingungen gespült.The so-called plate test was also carried out. The methodology is in the magazine »Fette; Soap; Anstrichmittel «, 74 [1972], pages 163 to 165. It was mainly used with water of 45 ° C / 16 ° d and the use of 0.5 g / I product as well as a mixed contamination from protein, fat and carbohydrates. The mixed soiling was used with 2 g / plate (saucer 14 cm in diameter; distributed in the cup recess); the soiled plates were rinsed after 15 hours of storage at ± 0 to + 5 ° C under the conditions specified above.
Zu der nachfolgenden Tabelle sind die Ergebnisse aufgeführt, die die Vorteile der erfindungsgemäßen Reinigungsmittel gegenüber handelsüblichen Produkten eindeutig demonstrieren..
Claims (4)
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
AT81102003T ATE6075T1 (en) | 1980-03-26 | 1981-03-18 | LIQUID DETERGENT. |
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
DE19803011550 DE3011550A1 (en) | 1980-03-26 | 1980-03-26 | LIQUID CLEANING AGENTS |
DE3011550 | 1980-03-26 |
Publications (2)
Publication Number | Publication Date |
---|---|
EP0036625A1 EP0036625A1 (en) | 1981-09-30 |
EP0036625B1 true EP0036625B1 (en) | 1984-02-01 |
Family
ID=6098301
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
EP81102003A Expired EP0036625B1 (en) | 1980-03-26 | 1981-03-18 | Liquid cleaning agents |
Country Status (3)
Country | Link |
---|---|
EP (1) | EP0036625B1 (en) |
AT (1) | ATE6075T1 (en) |
DE (2) | DE3011550A1 (en) |
Families Citing this family (10)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US4371461A (en) * | 1980-10-02 | 1983-02-01 | The Procter & Gamble Company | Liquid detergent compositions with tertiary alcohol skin feel additives |
US4595526A (en) * | 1984-09-28 | 1986-06-17 | Colgate-Palmolive Company | High foaming nonionic surfacant based liquid detergent |
ES8708009A1 (en) * | 1984-11-07 | 1987-09-01 | Procter & Gamble | Liquid detergent compositions. |
GB8602589D0 (en) * | 1986-02-03 | 1986-03-12 | Unilever Plc | Detergent compositions |
DE3726912A1 (en) * | 1987-08-13 | 1989-02-23 | Henkel Kgaa | LIQUID MEDIUM TO CLEAN HARD SURFACES |
GB8905551D0 (en) * | 1989-03-10 | 1989-04-19 | Unilever Plc | Detergent compositions |
DE68928569D1 (en) * | 1989-11-06 | 1998-03-05 | Colgate Palmolive Co | Softening heavy-duty detergent composition for laundry |
GB9201519D0 (en) * | 1992-01-24 | 1992-03-11 | Unilever Plc | Detergent compositions |
CA2205854A1 (en) * | 1994-11-23 | 1996-05-30 | Rita Erilli | Microemulsion light duty liquid cleaning compositions |
US6537958B1 (en) | 1999-11-10 | 2003-03-25 | The Procter & Gamble Company | Bleaching compositions |
Citations (4)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
DE2339991A1 (en) * | 1972-08-08 | 1974-02-28 | Nippon Unitol Co Ltd | DETERGENTS AND DETERGENTS |
US3985687A (en) * | 1974-12-26 | 1976-10-12 | Colgate-Palmolive Company | Liquid detergent compositions of controlled viscosities |
DD135288A1 (en) * | 1977-12-29 | 1979-04-25 | Horst Seibt | CLEANING AGENT FOR HARD SURFACES, PREFERABLY PLASTIC PLATES FROM POLYESTER RESINS |
DE2857292A1 (en) * | 1977-09-23 | 1980-02-28 | Procter & Gamble | ANIONIC SURFACE-CONTAINING DETERGENT WITH DIRT-REMOVING PROPERTIES |
Family Cites Families (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPS5347807B2 (en) * | 1973-05-08 | 1978-12-23 |
-
1980
- 1980-03-26 DE DE19803011550 patent/DE3011550A1/en active Granted
-
1981
- 1981-03-18 EP EP81102003A patent/EP0036625B1/en not_active Expired
- 1981-03-18 AT AT81102003T patent/ATE6075T1/en active
- 1981-03-18 DE DE8181102003T patent/DE3162080D1/en not_active Expired
Patent Citations (4)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
DE2339991A1 (en) * | 1972-08-08 | 1974-02-28 | Nippon Unitol Co Ltd | DETERGENTS AND DETERGENTS |
US3985687A (en) * | 1974-12-26 | 1976-10-12 | Colgate-Palmolive Company | Liquid detergent compositions of controlled viscosities |
DE2857292A1 (en) * | 1977-09-23 | 1980-02-28 | Procter & Gamble | ANIONIC SURFACE-CONTAINING DETERGENT WITH DIRT-REMOVING PROPERTIES |
DD135288A1 (en) * | 1977-12-29 | 1979-04-25 | Horst Seibt | CLEANING AGENT FOR HARD SURFACES, PREFERABLY PLASTIC PLATES FROM POLYESTER RESINS |
Also Published As
Publication number | Publication date |
---|---|
DE3011550A1 (en) | 1981-10-01 |
EP0036625A1 (en) | 1981-09-30 |
DE3011550C2 (en) | 1987-06-19 |
ATE6075T1 (en) | 1984-02-15 |
DE3162080D1 (en) | 1984-03-08 |
Similar Documents
Publication | Publication Date | Title |
---|---|---|
EP0216301B1 (en) | Liquid cleaning agent | |
DE2057353B2 (en) | Liquid detergents and cleaning agents | |
DE3305197A1 (en) | MELLOW LIQUID DETERGENT | |
DE3533977A1 (en) | STRONG FOAMING LIQUID FINE CLEANER BASED ON NON-IONIC SURFACTANTS | |
EP0379658A2 (en) | Washing, cleaning and/or body cleaning composition | |
EP0036625B1 (en) | Liquid cleaning agents | |
EP0306843A2 (en) | Thickened aqueous surfactant solutions, in particular for their use in the domain of cosmetic preparations | |
DE102010055742A1 (en) | Compositions containing secondary paraffin sulfonate and alcohol alkoxylate | |
DE3726911A1 (en) | WAITER PREPARATIONS OF IONIC TENSIDES WITH INCREASED VISCOSITY | |
DE4107414A1 (en) | LIQUID CLEANING AGENT CONTAINING SULFOLOIC ACIDS | |
EP0513138A1 (en) | Aqueous liquid cleaning agent. | |
DE3724500A1 (en) | ALKYLSULFATE ETHERSULPATE MIXTURES AND THEIR USE | |
DE102010055743A1 (en) | Compositions containing secondary paraffin sulfonate and alcohol alkoxylate | |
DE4324358A1 (en) | Solid synthetic compsn for cleaning and conditioning hair and skin for softness - contg mixt of strongly foaming anionic and amphoteric surfactants and minor amt of water-insol silicone, sufficiently mild for use on face avoiding irritation | |
EP1075502B1 (en) | Dishwashing detergent with an antibacterial effect | |
DE19753982A1 (en) | Dishwashing liquid with an antibacterial effect | |
EP0632824B1 (en) | Liquid cleaning products | |
EP0371339B1 (en) | Surfactant mixtures | |
EP0455657B1 (en) | Surface active mixtures | |
EP0912671A1 (en) | Hand dishwashing agent acceptable to the skin | |
EP0536199B1 (en) | Extra-mild shower gel and hair shampoo formulation with low tenside concentration | |
EP0519942B1 (en) | Cosmetic cleansing agent | |
EP0781318B1 (en) | Anhydrous surfactant mixtures | |
EP0383053A1 (en) | Liquid detergents | |
EP0442519A2 (en) | Self-preserving liquid tenside systems |
Legal Events
Date | Code | Title | Description |
---|---|---|---|
PUAI | Public reference made under article 153(3) epc to a published international application that has entered the european phase |
Free format text: ORIGINAL CODE: 0009012 |
|
AK | Designated contracting states |
Designated state(s): AT BE CH DE FR GB IT LU NL SE |
|
17P | Request for examination filed |
Effective date: 19811029 |
|
ITF | It: translation for a ep patent filed |
Owner name: STUDIO JAUMANN |
|
GRAA | (expected) grant |
Free format text: ORIGINAL CODE: 0009210 |
|
PGFP | Annual fee paid to national office [announced via postgrant information from national office to epo] |
Ref country code: CH Payment date: 19840130 Year of fee payment: 4 |
|
AK | Designated contracting states |
Designated state(s): AT BE CH DE FR GB IT LI LU NL SE |
|
PGFP | Annual fee paid to national office [announced via postgrant information from national office to epo] |
Ref country code: DE Payment date: 19840201 Year of fee payment: 4 |
|
REF | Corresponds to: |
Ref document number: 6075 Country of ref document: AT Date of ref document: 19840215 Kind code of ref document: T |
|
PGFP | Annual fee paid to national office [announced via postgrant information from national office to epo] |
Ref country code: FR Payment date: 19840227 Year of fee payment: 4 |
|
REF | Corresponds to: |
Ref document number: 3162080 Country of ref document: DE Date of ref document: 19840308 |
|
ET | Fr: translation filed | ||
PGFP | Annual fee paid to national office [announced via postgrant information from national office to epo] |
Ref country code: LU Payment date: 19840322 Year of fee payment: 4 |
|
PG25 | Lapsed in a contracting state [announced via postgrant information from national office to epo] |
Ref country code: LU Free format text: LAPSE BECAUSE OF NON-PAYMENT OF DUE FEES Effective date: 19840331 |
|
PGFP | Annual fee paid to national office [announced via postgrant information from national office to epo] |
Ref country code: BE Payment date: 19840331 Year of fee payment: 4 |
|
PLBI | Opposition filed |
Free format text: ORIGINAL CODE: 0009260 |
|
PGFP | Annual fee paid to national office [announced via postgrant information from national office to epo] |
Ref country code: SE Payment date: 19841231 Year of fee payment: 5 |
|
26 | Opposition filed |
Opponent name: BLENDAX-WERKE R. SCHNEIDER GMBH & CO. Effective date: 19841031 |
|
NLR1 | Nl: opposition has been filed with the epo |
Opponent name: BLENDAX-WERKE R. SCHNEIDER GMBH & CO |
|
PGFP | Annual fee paid to national office [announced via postgrant information from national office to epo] |
Ref country code: AT Payment date: 19860221 Year of fee payment: 6 |
|
PGFP | Annual fee paid to national office [announced via postgrant information from national office to epo] |
Ref country code: NL Payment date: 19860331 Year of fee payment: 6 |
|
RDAG | Patent revoked |
Free format text: ORIGINAL CODE: 0009271 |
|
STAA | Information on the status of an ep patent application or granted ep patent |
Free format text: STATUS: PATENT REVOKED |
|
27W | Patent revoked |
Effective date: 19860613 |
|
REG | Reference to a national code |
Ref country code: CH Ref legal event code: PL |
|
NLR2 | Nl: decision of opposition | ||
GBPR | Gb: patent revoked under art. 102 of the ep convention designating the uk as contracting state | ||
BERE | Be: lapsed |
Owner name: HENKEL K.G.A.A. Effective date: 19870331 |
|
REG | Reference to a national code |
Ref country code: FR Ref legal event code: ST |
|
EUG | Se: european patent has lapsed |
Ref document number: 81102003.1 Effective date: 19880215 |