EP0508507A1 - Liquid dishwashing composition - Google Patents

Liquid dishwashing composition Download PDF

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Publication number
EP0508507A1
EP0508507A1 EP92200679A EP92200679A EP0508507A1 EP 0508507 A1 EP0508507 A1 EP 0508507A1 EP 92200679 A EP92200679 A EP 92200679A EP 92200679 A EP92200679 A EP 92200679A EP 0508507 A1 EP0508507 A1 EP 0508507A1
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group
compounds
dishwashing composition
amphoteric
alkyl
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German (de)
French (fr)
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EP0508507B1 (en
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Jadwiga Palicka
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Nouryon Surface Chemistry AB
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Berol Nobel AB
Akzo Nobel Surface Chemistry AB
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    • CCHEMISTRY; METALLURGY
    • C11ANIMAL OR VEGETABLE OILS, FATS, FATTY SUBSTANCES OR WAXES; FATTY ACIDS THEREFROM; DETERGENTS; CANDLES
    • C11DDETERGENT COMPOSITIONS; USE OF SINGLE SUBSTANCES AS DETERGENTS; SOAP OR SOAP-MAKING; RESIN SOAPS; RECOVERY OF GLYCEROL
    • C11D1/00Detergent compositions based essentially on surface-active compounds; Use of these compounds as a detergent
    • C11D1/88Ampholytes; Electroneutral compounds
    • C11D1/94Mixtures with anionic, cationic or non-ionic compounds

Definitions

  • the present invention relates to liquid dishwashing compositions and more particularly to such compositions which contain an anionic tenside, a combination of specific amphoteric surface active compounds and an alkyl polyglycoside.
  • dishwashing compositions are primarily intended for hand dishwashing and are as a rule aqueous solutions containing anionic ten-sides, such as alkyl sulfonates and alkyl ether sulfates, as essential component. These dishwashing agents are entirely satisfactory with regard to cleaning effect, foam forming effect and foam stability. However, the dishwashing compositions based on this type of anionic surface active agents are not satisfactory with regard to mildness to skin, since they have a certain irritating and allergy causing effect. There is thus a great interest in producing dishwashing compositions which are mild to the skin and at the same time give a good cleaning effect.
  • anionic ten-sides such as alkyl sulfonates and alkyl ether sulfates
  • nonionic alkyl polyglycosides have become of commercial interest for use in dishwashing formulations and other cleaning formulations.
  • These nonionic surface active compounds which are products based on natural raw materials, are advantageous for use in dishwashing and other cleaning compositions in that they are mild to the skin, have high biodegradability and good compatibility with other types of surfactants.
  • Alkyl polyglycosides are per se well-known compounds and extensively disclosed. Their use as surfactants in combination with other types of surfactants is also well-known.
  • the European patent application 0341071 discloses detergent compositions which are particularly useful for manual dishwashing and which contain an alkyl polyglycoside surfactant, an anionic surfactant, a surface active betaine and/or amine oxide.
  • dishwashing compositions are obtained when anionic tensides are used together with an alkyl polyglycoside and together with a combination of certain amphoteric compounds.
  • Liquid dishwashing compositions containing anionic surface active agents, alkyl polyglycoside and the combination of specific amphoteric compounds have extremely good mildness to skin and good foaming properties and they further give a low biological load and are more efficient than a dishwashing composition based on anionic tenside, an alkyl polyglycoside and an amphoteric alkyl betaine surfactant.
  • Dishwashing compositions according to the present invention are particularly suitable for manual washing, of glass, china, kitchen utensils etc, thanks to their mildness.
  • amphoteric surface active compounds of type a) can be characterized by the general formula (I) wherein R is a hydrocarbon group having from 7 to 22 carbon atoms, n is 0 or 1, A is a carbonyl group [C(O)], a group (OCH2CH2) z or (OCH2CH2CH2) z wherein z is an integer of from 1 to 5, R1 is hydrogen or a lower alkyl group, x is 2 or 3, y is an integer of 0 to 4, Q is the group -R2COOM wherein R2 is an alkylene group having from 1 to 6 carbon atoms and M is hydrogen or an ion from the groups alkali metals, alkaline earth metals, ammonium and substituted ammonium and B is hydrogen or a group Q as defined.
  • R is a hydrocarbon group having from 7 to 22 carbon atoms
  • n is 0 or 1
  • A is a carbonyl group [C(O)], a group (OCH2CH2)
  • Amphoteric compounds of the above type are per se known and used in cleaning compositions and shampoo compositions. They are for example described in the European patent applications 160507, 162600 and 214868.
  • R is a hydrocarbon group having from 7 to 22 carbon atoms and suitably from 11 to 22 carbon atoms.
  • the hydrocarbon group R can be straight or branched, saturated or unsaturated and optionally contain substituents such as hydroxyl groups.
  • the group R can also be a cycloalkyl-alkyl group, an aralkyl or aralkenyl group where the alkyl or alkenyl group contains at least 6 carbon atoms.
  • R is preferably an alkyl or alkenyl group and it is particularly preferred that R is a hydrocarbon group originating from coco, tallow or oleic fatty acid.
  • the amphoteric compounds of formula (I) can, as indicated, contain a group A which is a carbonyl group or one or several ethoxy- or propoxy-groups. When A is ethoxy or propoxy groups ethoxy groups are preferred and A is then especially one such group. Compounds which do not contain a group A, ie in which n is 0, are preferred.
  • R1 in the given formula is hydrogen or a lower alkyl group, suitably with 1 to 6 carbon atoms and is preferably hydrogen or a methyl group.
  • x is 2 or 3 and y is suitably 2, 3 or 4 and preferably 2 or 3.
  • the group R2 is suitably a methylene or an ethylene group, preferably a methylene group.
  • M is hydrogen or an ion from the groups alkali metals, alkaline earth metals, ammonium or substituted ammonium such as for example mono-, di- or trihydroxyethylammonium. M is preferably a sodium ion.
  • Preferred compounds of the formula (I) have the formula (II): wherein Q is CH2-COOM or CH2CH2COOM, y is 1, 2 or 3 and wherein M, R, x and B have the above given meanings. x is suitably 3 and all groups B are suitably groups Q.
  • R in these compounds suitably originates from tallow, oleic or coco fatty acid.
  • amphoteric compounds of the above given formulae are used in combination with amphoteric compounds containing a carbonyl group.
  • These amphoteric compounds, of type b), are either such which can be characterized by the general formula (III) or amido betaines as shown in formula (IV). Mixtures of these two types of amphoteric compounds can also be used.
  • Compounds of formula (III) are wherein R, y, Q and B have the same meaning as given for compounds of formula (I), whereby, however, one group B is the group -CH2CHR'OH, wherein R' is H or CH3.
  • the suitable and preferred definitions for R and for M in the group Q are as given for compounds of formula (I).
  • Most suitable are compounds of formula (III) wherein y is 1 and Q is the group -CH2COOM.
  • Amphoteric compounds of formulae IIIa and IIIb are commercially available as mixtures and usually with a weight ratio of compounds of formula IIIa to compounds of formula IIIb within the range of 1:10 to 10:1.
  • Amphoteric compounds of the amido betaine type containing a carbonyl group can be characterized by the general formula (IV) wherein R is a longer hydrophobic hydrocarbon group, which suitably is a saturated or unsaturated, straight or branched, aliphatic hydrocarbon group with at least 7 carbon atoms. R suitably has from 7 to 21 carbon atoms and preferably is an alkyl or alkenyl group with from 11 to 17 carbon atoms, R' is an alkyl or hydroxyalkyl group with from 1 to 4 carbon atoms. Most suitably both groups R' are methyl groups, and n is 1 or 2. M is preferably hydrogen or a sodium ion.
  • amphoteric compounds of type a) act primarily as detoxifying tensides while those of type b) act primarily as tensides, viscosity modifiers and suds formers.
  • Suitable weight ratios between amphoteric compounds of type a) and type b) is within the range of from 1:10 to 10:1 and preferably within the range of from 1:5 to 5:1.
  • the total amount of the defined amphoteric compounds in the dishwashing compositions is suitably from 1 to 20 per cent by weight and preferably from 1.5 to 15 per cent by weight.
  • Amphoteric compounds of the above given formulae are commercially available and sold under the trade name Ampholak (R) by Berol Nobel AB, Sweden.
  • the above combination of amphoteric compounds can partly replace anionic tensides and be used in liquid dishwashing compositions together with an alkyl polyglycoside to give very mild and efficient compositions with good foaming properties.
  • the mildness which is obtained is dependent not only on the use of the alkyl polyglycoside but also on an efficient detoxification of anionic tensides through formation of mixed micelles of the anionic surface active compounds and the specific amphoteric surface active compounds.
  • the very low critical micelle concentration for the specific amphoteric compounds is hereby utilized. The desired effect is thus obtained with very small amounts of amphoteric compound, particularly of those of the above given formulae I and II.
  • the alkyl polyglycosides, or sugar ethers, which are used in the present compositions are per se known nonionic surface active compounds which have a hydrophilic polysaccharide head group and a hydrophobic hydrocarbon substituent.
  • the hydrophilic saccharide units can for example be fructoside or glucoside units, glucoside units being preferred.
  • the alkyl polyglycosides suitably contain an average of from 1 to 5 saccharide units and preferably from 1.2 to 1.5 units.
  • the hydrophobic hydrocarbon group, an alkyl or alkenyl group, preferably an alkyl group suitably has from about 8 to about 20 carbon atoms and preferably from 10 to 18 carbon atoms.
  • alkyl polyglycosides are commercially available, for example from Henkel under the trade name Plantaren (R) APG.
  • the amount of alkyl polyglycosides in the present compositions is suitably from 1 to 15 per cent by weight and preferably from 1.5 to 4 per cent by weight.
  • an alkyl polyglycoside and anionic tensides which normally are water soluble sulfonates or sulfates, in liquid dishwashing compositions, the latter can be replaced to a certain extent and hereby a dishwashing composition is obtained which is advantageous from a biological point of view and advantageous with regard to mildness at use.
  • the present compositions also make it possible to substantially reduce the total amount of active components for obtaining the same dishwashing performance as with known compositions based on solely anionic tensides and as with compositions containing anionic tenside, an alkyl betaine amphoteric compound and an alkyl polyglycoside.
  • anionic tensides of the above mentioned types are also present, but in lower amounts than usual.
  • the total amount of amphoteric, nonionic and anionic surface active agents at most 90 per cent by weight are anionic tensides.
  • the amount of anionic tenside is suitably within the range of from 85 to 30 per cent by weight, based on the total amount of amphoteric surface active compounds, nonionic alkyl polyglycoside and anionic surface active compounds, and is particularly within the range of from 85 to 60 per cent by weight.
  • the anionic tensides are, as indicated above, water soluble sulfates or sulfonates, and then particularly alkyl sulfates, alkyl ether sulfates, alkyl sulfonates, alkyl aryl sulfonates, wherein the alkyl group usually contains from 8 to 22 carbon atoms.
  • alkyl group usually contains from 8 to 22 carbon atoms.
  • alkyl group usually contains from 8 to 22 carbon atoms.
  • anionic tensides containing ether groups these are usually ethylene oxide groups and the compounds normally contain between 1 and 10 such groups per molecule.
  • the cations are usually alkali metals, alkaline earth metals, ammonium or amines such as mono-, di- and triethanol amine cations.
  • anionic tensides can be mentioned sodium lauryl sulfonate, sodium lauryl ether sulfate with two or three ethylene oxide groups, the corresponding ammonium or ethanol amine salts, sodium or other salts of dodecyl benzene sulfonic acid and alkyl benzene sulfonic acid wherein the alkyl group contains an average of from 11 to 13 carbon atoms. At least two different anionic tensides are often used in the dishwashing compositions.
  • the present dishwashing compositions are liquid and the main component for this is of course preferably water.
  • Water used in liquid dishwashing compositions is often deionized but other types of water can also be used.
  • Other liquid solvents can of course be included, such as for example lower alcohols and glycols and lower alkyl ethers of the glycols. These types of solvents are normally present, if at all present, in minor amounts. As some specific examples can be mentioned ethanol, isopropanol, ethylene glycol etc.. Solvents are sometimes included mainly for preservation.
  • One advantage of the present compositions is, however, that since they contain amphoteric compounds of the type according to formula (I) no solvent is required in order to obtain preservative effect.
  • the present dishwashing compositions can be prepared in per se conventional manner by simple mixing of the components and they can of course also be used in conventional manner. Normal dosage is about 0.2 g/l dish liquor of a dishwashing composition with a total dry content of from about 10 to about 45 per cent by weight.
  • the dishwashing compositions can of course also contain other conventionally used additives for improvement of different properties such as thickeners, antibacterial agents, colorants, pigments, perfumes etc..
  • Other amphoteric compounds can also be present if desired, such as betaines, and also other nonionic tensides.
  • the compositions should be essentially free from cationic surface active agents.
  • the dishwashing compositions of the present invention have good foam properties and no special foam booster or foam stabilizing compounds are thus necessary.
  • foam boosting compounds can of course be included in the present compositions and as examples of such can be mentioned amides and amine oxides containing at least one longer hydrophobic hydrocarbon group, ie a fatty acid residue having at least 7 carbon atoms and suitably up to 22 carbon atoms.
  • Dishwashing compositions were prepared as follows (all amounts given are as 100% active substance): Composition I - Reference: 11.2 g of sodium salt of linear alkyl benzene sulfonate with C12 to C18 alkyl groups, 5.6 g of sodium lauryl ether sulfate with 3 ethylene oxide groups, 2.1 g of alkyl polyglycoside, 2.1 g of a C12/C14 alkyl dimethyl betaine sold under the name Amphoteen 24 and 79 g of water.
  • Composition II According to the invention: 11.2 g of sodium salt of linear alkyl benzene sulfonate with C12 to C18 alkyl groups, 5.6 g of sodium lauryl ether sulfate with 3 ethylene oxide groups, 2.1 g of a mixture of two different amphoteric compounds, a 1:2 mixture of amphoteric compounds sold under the trade marks Ampholak (R) 7TX and Ampholak (R) XCO-30, respectively, - the first mentioned amphoteric compound can chemically be characterized as tallowampho polycarboxyglycinate and falls under the definition of compounds according to formula II and the last mentioned one can chemically be characterized as cocoamphocarboxyglycinate and contains a carbonyl group and comprises a mixture of compounds defined in formulae IIIa and IIIb -, 2.1 g of alkyl polyglycoside and 79 g of water.
  • Composition III Reference: 11.2 g of alkane (C12-C18) sulfonate, 5.6 g of sodium lauryl ether sulfate with 3 ethylene oxide groups, 2.1 g of alkyl polyglycoside, 2.1 g of alkyl dimethyl betaine and 79 g of water.
  • Composition IV According to the invention: 11.2 g of alkane C12-C18 sulfonate, 5.6 g of sodium lauryl ether sulfate with 3 ethylene oxide groups, 2.1 g of the same mixture of two amphoteric compounds as in Composition II, 2.1 g of alkyl polyglycoside and 79 g of water.
  • the alkyl polyglycoside in all compositions was an alkyl polyglycoside sold under the name Plantaren (R) APG 600 by Henkel. It has an average number of saccharide units of 1,4 and a C12-14-16 hydrocarbon group.
  • the alkyl dimethyl betaine used in reference compositions I and III was a C12-C14 alkyl dimethyl betaine sold under the name of Amphoteen (R) 24 by Berol Nobel AB.
  • composition Efficiency Index I Composition Efficiency Index I - Reference 1 II - According to the invention 1 III - Reference 1.25 IV - According to the invention 1.8
  • Composition II according to the invention had the same efficiency index as the reference but for Composition IV according to the invention a considerably better efficiency was obtained in comparison with the reference Composition III.
  • Dishwashing performance of the compositions was assessed by the practical dishwashing tests. 1 ml beef tallow with an iodine number of 55.1 was applied on each plate and the plates were allowed to dry over one night at ambient temperature. 8 l of water with a concentration of 0.2 g/l of each tested composition and with a hardness of 20°dH were used at a temperature of 45+-2°C. After the initial generation of foam the dried plates covered with beef tallow were cleaned with a brush until the foam collapsed. The results were recorded as the number of washed plates and set in relation to the results obtained with composition 1. Composition Number of washed plates Dishwashing performance % I - Ref. 8 100 II - Invention 10 125 III - Ref. 16 200 IV - Invention 20 250
  • composition according to the invention was prepared: 8.98 g of sodium lauryl ether sulfate with 2 ethylene oxide groups, 2 g of alkyl polyglycoside Plantaren (R) APG 600, 6.67 g of cocoamido betaine, 3.32 g of Ampholak (R) 7TX and 79.03 g of water.

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Abstract

Liquid dishwashing compositions containing an anionic surface active agent, an alkyl polyglycoside and a combination of two types of amphoteric compounds. The combination of amphoteric surface active compounds and the alkyl polyglycoside partly replace anionic tensides to give dishwashing compositions which are mild and satisfactory with regard to environment.

Description

  • The present invention relates to liquid dishwashing compositions and more particularly to such compositions which contain an anionic tenside, a combination of specific amphoteric surface active compounds and an alkyl polyglycoside.
  • The most common commercial liquid dishwashing compositions are primarily intended for hand dishwashing and are as a rule aqueous solutions containing anionic ten-sides, such as alkyl sulfonates and alkyl ether sulfates, as essential component. These dishwashing agents are entirely satisfactory with regard to cleaning effect, foam forming effect and foam stability. However, the dishwashing compositions based on this type of anionic surface active agents are not satisfactory with regard to mildness to skin, since they have a certain irritating and allergy causing effect. There is thus a great interest in producing dishwashing compositions which are mild to the skin and at the same time give a good cleaning effect.
  • In the last few years nonionic alkyl polyglycosides have become of commercial interest for use in dishwashing formulations and other cleaning formulations. These nonionic surface active compounds, which are products based on natural raw materials, are advantageous for use in dishwashing and other cleaning compositions in that they are mild to the skin, have high biodegradability and good compatibility with other types of surfactants. Alkyl polyglycosides are per se well-known compounds and extensively disclosed. Their use as surfactants in combination with other types of surfactants is also well-known. The European patent application 0341071 discloses detergent compositions which are particularly useful for manual dishwashing and which contain an alkyl polyglycoside surfactant, an anionic surfactant, a surface active betaine and/or amine oxide. According to the present invention it has been found that surprisingly good dishwashing compositions are obtained when anionic tensides are used together with an alkyl polyglycoside and together with a combination of certain amphoteric compounds. Liquid dishwashing compositions containing anionic surface active agents, alkyl polyglycoside and the combination of specific amphoteric compounds have extremely good mildness to skin and good foaming properties and they further give a low biological load and are more efficient than a dishwashing composition based on anionic tenside, an alkyl polyglycoside and an amphoteric alkyl betaine surfactant.
  • The present invention thus relates to a dishwashing composition as further defined in the appended claims. Dishwashing compositions according to the present invention are particularly suitable for manual washing, of glass, china, kitchen utensils etc, thanks to their mildness.
  • In the dishwashing compositions of the present invention a combination of two types of amphoteric compounds is used and they are in the following designated as type a) and type b). The amphoteric surface active compounds of type a) can be characterized by the general formula (I)
    Figure imgb0001

    wherein R is a hydrocarbon group having from 7 to 22 carbon atoms, n is 0 or 1, A is a carbonyl group [C(O)], a group (OCH₂CH₂)z or (OCH₂CH₂CH₂)z wherein z is an integer of from 1 to 5, R₁ is hydrogen or a lower alkyl group, x is 2 or 3, y is an integer of 0 to 4, Q is the group -R₂COOM wherein R₂ is an alkylene group having from 1 to 6 carbon atoms and M is hydrogen or an ion from the groups alkali metals, alkaline earth metals, ammonium and substituted ammonium and B is hydrogen or a group Q as defined.
  • Amphoteric compounds of the above type are per se known and used in cleaning compositions and shampoo compositions. They are for example described in the European patent applications 160507, 162600 and 214868. In the amphoteric surface active compounds of the above given formula which are used in the present dishwashing compositions R is a hydrocarbon group having from 7 to 22 carbon atoms and suitably from 11 to 22 carbon atoms. The hydrocarbon group R can be straight or branched, saturated or unsaturated and optionally contain substituents such as hydroxyl groups. The group R can also be a cycloalkyl-alkyl group, an aralkyl or aralkenyl group where the alkyl or alkenyl group contains at least 6 carbon atoms. R is preferably an alkyl or alkenyl group and it is particularly preferred that R is a hydrocarbon group originating from coco, tallow or oleic fatty acid. The amphoteric compounds of formula (I) can, as indicated, contain a group A which is a carbonyl group or one or several ethoxy- or propoxy-groups. When A is ethoxy or propoxy groups ethoxy groups are preferred and A is then especially one such group. Compounds which do not contain a group A, ie in which n is 0, are preferred. R₁ in the given formula is hydrogen or a lower alkyl group, suitably with 1 to 6 carbon atoms and is preferably hydrogen or a methyl group. x is 2 or 3 and y is suitably 2, 3 or 4 and preferably 2 or 3. The group R₂ is suitably a methylene or an ethylene group, preferably a methylene group. M is hydrogen or an ion from the groups alkali metals, alkaline earth metals, ammonium or substituted ammonium such as for example mono-, di- or trihydroxyethylammonium. M is preferably a sodium ion.
  • Preferred compounds of the formula (I) have the formula (II):
    Figure imgb0002

    wherein Q is CH₂-COOM or CH₂CH₂COOM, y is 1, 2 or 3 and wherein M, R, x and B have the above given meanings. x is suitably 3 and all groups B are suitably groups Q.
  • Mixtures of the amphoteric compounds with different values for y are especially preferred. R in these compounds suitably originates from tallow, oleic or coco fatty acid.
  • In the present compositions the amphoteric compounds of the above given formulae are used in combination with amphoteric compounds containing a carbonyl group. These amphoteric compounds, of type b), are either such which can be characterized by the general formula (III) or amido betaines as shown in formula (IV). Mixtures of these two types of amphoteric compounds can also be used. Compounds of formula (III) are
    Figure imgb0003

    wherein R, y, Q and B have the same meaning as given for compounds of formula (I), whereby, however, one group B is the group -CH₂CHR'OH, wherein R' is H or CH₃. The suitable and preferred definitions for R and for M in the group Q are as given for compounds of formula (I). Most suitable are compounds of formula (III) wherein y is 1 and Q is the group -CH₂COOM. As typical examples can be given compounds of formulae (IIIa) and/or (IIIb)
    Figure imgb0004
  • Amphoteric compounds of formulae IIIa and IIIb are commercially available as mixtures and usually with a weight ratio of compounds of formula IIIa to compounds of formula IIIb within the range of 1:10 to 10:1.
  • Amphoteric compounds of the amido betaine type containing a carbonyl group can be characterized by the general formula (IV)
    Figure imgb0005

    wherein R is a longer hydrophobic hydrocarbon group, which suitably is a saturated or unsaturated, straight or branched, aliphatic hydrocarbon group with at least 7 carbon atoms. R suitably has from 7 to 21 carbon atoms and preferably is an alkyl or alkenyl group with from 11 to 17 carbon atoms, R' is an alkyl or hydroxyalkyl group with from 1 to 4 carbon atoms. Most suitably both groups R' are methyl groups, and n is 1 or 2. M is preferably hydrogen or a sodium ion.
  • The amphoteric compounds of type a) act primarily as detoxifying tensides while those of type b) act primarily as tensides, viscosity modifiers and suds formers. Suitable weight ratios between amphoteric compounds of type a) and type b) is within the range of from 1:10 to 10:1 and preferably within the range of from 1:5 to 5:1. The total amount of the defined amphoteric compounds in the dishwashing compositions is suitably from 1 to 20 per cent by weight and preferably from 1.5 to 15 per cent by weight.
  • Amphoteric compounds of the above given formulae are commercially available and sold under the trade name Ampholak(R) by Berol Nobel AB, Sweden.
  • According to the present invention it has been found that the above combination of amphoteric compounds can partly replace anionic tensides and be used in liquid dishwashing compositions together with an alkyl polyglycoside to give very mild and efficient compositions with good foaming properties. The mildness which is obtained is dependent not only on the use of the alkyl polyglycoside but also on an efficient detoxification of anionic tensides through formation of mixed micelles of the anionic surface active compounds and the specific amphoteric surface active compounds. The very low critical micelle concentration for the specific amphoteric compounds is hereby utilized. The desired effect is thus obtained with very small amounts of amphoteric compound, particularly of those of the above given formulae I and II.
  • The alkyl polyglycosides, or sugar ethers, which are used in the present compositions are per se known nonionic surface active compounds which have a hydrophilic polysaccharide head group and a hydrophobic hydrocarbon substituent. The hydrophilic saccharide units can for example be fructoside or glucoside units, glucoside units being preferred. The alkyl polyglycosides suitably contain an average of from 1 to 5 saccharide units and preferably from 1.2 to 1.5 units. The hydrophobic hydrocarbon group, an alkyl or alkenyl group, preferably an alkyl group, suitably has from about 8 to about 20 carbon atoms and preferably from 10 to 18 carbon atoms. The alkyl polyglycosides are commercially available, for example from Henkel under the trade name Plantaren(R)APG. The amount of alkyl polyglycosides in the present compositions is suitably from 1 to 15 per cent by weight and preferably from 1.5 to 4 per cent by weight.
  • By using the combination of amphoteric compounds, as above defined, an alkyl polyglycoside and anionic tensides, which normally are water soluble sulfonates or sulfates, in liquid dishwashing compositions, the latter can be replaced to a certain extent and hereby a dishwashing composition is obtained which is advantageous from a biological point of view and advantageous with regard to mildness at use. In addition to these advantages, the present compositions also make it possible to substantially reduce the total amount of active components for obtaining the same dishwashing performance as with known compositions based on solely anionic tensides and as with compositions containing anionic tenside, an alkyl betaine amphoteric compound and an alkyl polyglycoside.
  • In the present compositions anionic tensides of the above mentioned types are also present, but in lower amounts than usual. Of the total amount of amphoteric, nonionic and anionic surface active agents at most 90 per cent by weight are anionic tensides. The amount of anionic tenside is suitably within the range of from 85 to 30 per cent by weight, based on the total amount of amphoteric surface active compounds, nonionic alkyl polyglycoside and anionic surface active compounds, and is particularly within the range of from 85 to 60 per cent by weight. The anionic tensides are, as indicated above, water soluble sulfates or sulfonates, and then particularly alkyl sulfates, alkyl ether sulfates, alkyl sulfonates, alkyl aryl sulfonates, wherein the alkyl group usually contains from 8 to 22 carbon atoms. For anionic tensides containing ether groups these are usually ethylene oxide groups and the compounds normally contain between 1 and 10 such groups per molecule. The cations are usually alkali metals, alkaline earth metals, ammonium or amines such as mono-, di- and triethanol amine cations. As some specific examples of anionic tensides can be mentioned sodium lauryl sulfonate, sodium lauryl ether sulfate with two or three ethylene oxide groups, the corresponding ammonium or ethanol amine salts, sodium or other salts of dodecyl benzene sulfonic acid and alkyl benzene sulfonic acid wherein the alkyl group contains an average of from 11 to 13 carbon atoms. At least two different anionic tensides are often used in the dishwashing compositions.
  • The present dishwashing compositions are liquid and the main component for this is of course preferably water. Water used in liquid dishwashing compositions is often deionized but other types of water can also be used. Other liquid solvents can of course be included, such as for example lower alcohols and glycols and lower alkyl ethers of the glycols. These types of solvents are normally present, if at all present, in minor amounts. As some specific examples can be mentioned ethanol, isopropanol, ethylene glycol etc.. Solvents are sometimes included mainly for preservation. One advantage of the present compositions is, however, that since they contain amphoteric compounds of the type according to formula (I) no solvent is required in order to obtain preservative effect.
  • The present dishwashing compositions can be prepared in per se conventional manner by simple mixing of the components and they can of course also be used in conventional manner. Normal dosage is about 0.2 g/l dish liquor of a dishwashing composition with a total dry content of from about 10 to about 45 per cent by weight.
  • The dishwashing compositions can of course also contain other conventionally used additives for improvement of different properties such as thickeners, antibacterial agents, colorants, pigments, perfumes etc.. Other amphoteric compounds can also be present if desired, such as betaines, and also other nonionic tensides. The compositions should be essentially free from cationic surface active agents. The dishwashing compositions of the present invention have good foam properties and no special foam booster or foam stabilizing compounds are thus necessary. However, if desired foam boosting compounds can of course be included in the present compositions and as examples of such can be mentioned amides and amine oxides containing at least one longer hydrophobic hydrocarbon group, ie a fatty acid residue having at least 7 carbon atoms and suitably up to 22 carbon atoms.
  • As example of a complete dishwashing composition according to the invention as concerns the main essential components those listed below can be given, wherein the ratios between types of compounds are adjusted to fall within the above given limits:
    Combination of
    amphoteric compounds 1 - 15 % by weight
    Alkyl polyglycoside 1 - 15 % by weight
    Anionic tenside 2 - 15 % by weight
    Water to 100 per cent by weight
  • The invention is further illustrated in the following examples, which, however, are not intended to limit the same. Parts and per cent relate to parts by weight and per cent by weight respectively, unless otherwise stated.
  • Example 1
  • Dishwashing compositions were prepared as follows (all amounts given are as 100% active substance):
    Composition I - Reference: 11.2 g of sodium salt of linear alkyl benzene sulfonate with C12 to C18 alkyl groups, 5.6 g of sodium lauryl ether sulfate with 3 ethylene oxide groups, 2.1 g of alkyl polyglycoside, 2.1 g of a C12/C14 alkyl dimethyl betaine sold under the name Amphoteen 24 and 79 g of water.
    Composition II - According to the invention: 11.2 g of sodium salt of linear alkyl benzene sulfonate with C12 to C18 alkyl groups, 5.6 g of sodium lauryl ether sulfate with 3 ethylene oxide groups, 2.1 g of a mixture of two different amphoteric compounds, a 1:2 mixture of amphoteric compounds sold under the trade marks Ampholak(R)7TX and Ampholak (R) XCO-30, respectively, - the first mentioned amphoteric compound can chemically be characterized as tallowampho polycarboxyglycinate and falls under the definition of compounds according to formula II and the last mentioned one can chemically be characterized as cocoamphocarboxyglycinate and contains a carbonyl group and comprises a mixture of compounds defined in formulae IIIa and IIIb -, 2.1 g of alkyl polyglycoside and 79 g of water.
    Composition III - Reference: 11.2 g of alkane (C12-C18) sulfonate, 5.6 g of sodium lauryl ether sulfate with 3 ethylene oxide groups, 2.1 g of alkyl polyglycoside, 2.1 g of alkyl dimethyl betaine and 79 g of water.
    Composition IV - According to the invention: 11.2 g of alkane C12-C18 sulfonate, 5.6 g of sodium lauryl ether sulfate with 3 ethylene oxide groups, 2.1 g of the same mixture of two amphoteric compounds as in Composition II, 2.1 g of alkyl polyglycoside and 79 g of water.
  • The alkyl polyglycoside in all compositions was an alkyl polyglycoside sold under the name Plantaren(R) APG 600 by Henkel. It has an average number of saccharide units of 1,4 and a C12-14-16 hydrocarbon group. The alkyl dimethyl betaine used in reference compositions I and III was a C12-C14 alkyl dimethyl betaine sold under the name of Amphoteen(R)24 by Berol Nobel AB.
  • All four compositions were tested by titration of 2 g/l of the solutions with béchamel sauce. Foam heights were determined and plotted against the amount of béchamel sauce. The areas of the diagrams were integrated and weighed and presented as efficiency versus content of amphoteric compound. The area for reference Composition I was set as efficiency 1. The efficiency index for the compositions are shown in the following table.
    Composition Efficiency Index
    I - Reference 1
    II - According to the invention 1
    III - Reference 1.25
    IV - According to the invention 1.8
  • As can be seen, Composition II according to the invention had the same efficiency index as the reference but for Composition IV according to the invention a considerably better efficiency was obtained in comparison with the reference Composition III.
  • Dishwashing performance of the compositions was assessed by the practical dishwashing tests. 1 ml beef tallow with an iodine number of 55.1 was applied on each plate and the plates were allowed to dry over one night at ambient temperature. 8 l of water with a concentration of 0.2 g/l of each tested composition and with a hardness of 20°dH were used at a temperature of 45+-2°C. After the initial generation of foam the dried plates covered with beef tallow were cleaned with a brush until the foam collapsed. The results were recorded as the number of washed plates and set in relation to the results obtained with composition 1.
    Composition Number of washed plates Dishwashing performance %
    I - Ref. 8 100
    II - Invention 10 125
    III - Ref. 16 200
    IV - Invention 20 250
  • From this table it can be seen that both compositions according to the invention gave substantially better dishwashing performance than the reference compositions.
  • Example 2
  • The following composition according to the invention was prepared: 8.98 g of sodium lauryl ether sulfate with 2 ethylene oxide groups, 2 g of alkyl polyglycoside Plantaren (R) APG 600, 6.67 g of cocoamido betaine, 3.32 g of Ampholak(R) 7TX and 79.03 g of water.
  • The dishwashing performance of this composition was evaluated in accordance with Example 1. 17 plates were washed. It should here be noted that this composition was based on solely sodium lauryl ether sulfate as anionic tenside, which generally means lower washing performance.

Claims (10)

  1. A liquid dishwashing composition, characterized in that it comprises
    a) an anionic surface active agent
    b) an alkyl polyglycoside and
    c) a combination of amphoteric compounds, comprising
    1) an amphoteric compound of type a) which has the general formula (I)
    Figure imgb0006
    wherein R is a hydrocarbon group having from 7 to 22 carbon atoms, n is 0 or 1, A is a carbonyl group [C(O)], a group (OCH₂CH₂)z or (OCH₂CH₂CH₂)z wherein z is an integer of from 1 to 5, R₁ is hydrogen or a lower alkyl group, x is 2 or 3, y is an integer of 0 to 4, Q is the group -R₂COOM wherein R₂ is an alkylene group having from 1 to 6 carbon atoms and M is hydrogen or an ion from the groups alkali metals, alkaline earth metals, ammonium and substituted ammonium and B is hydrogen or a group Q as defined, and
    2) an amphoteric compound of type b) which contains a carbonyl group and which has the general formula (III)
    Figure imgb0007
    wherein R, y, Q and B have the same meaning as given for compounds of formula (I), whereby, however, one group B is the group -CH₂CHR'OH, wherein R' is H or CH₃, and/or an amphoteric compound which has the general formula (IV)
    Figure imgb0008
    wherein R has the same meaning as given for compounds of formula (I), R' is an alkyl or hydroxyalkyl group with from 1 to 4 carbon atoms, n is 1 or 2 and M is hydrogen or a sodium ion.
  2. A dishwashing composition according to claim 1, characterized in that the amphoteric compound of type a) has the general formula (II):
    Figure imgb0009
    wherein Q is CH₂-COOM or CH₂CH₂COOM, y is 1, 2 or 3 and wherein M, R, x and B are as defined in claim 1.
  3. A dishwashing composition according to claim 1, characterized in that the amphoteric compound of type b) which contains a carbonyl group has the general formula (IIIa) and/or (IIIb)
    Figure imgb0010
    wherein R is a hydrocarbon group having from 7 to 22 carbon atoms.
  4. A dishwashing composition according to claim 1, 2 or 3, characterized in that R in the amphoteric compounds is an alkyl or alkenyl group with from 11 to 22 carbon atoms.
  5. A dishwashing composition according to any of the preceding claims, characterized in that the weight ratio of amphoteric compound of type a) to amphoteric compound of type b) is within the range of from 1:10 to 10:1.
  6. A dishwashing composition according to any of claims 1 to 5, characterized in that it comprises the combination of amphoteric compounds in a total amount of from 1 to 20 per cent by weight.
  7. A dishwashing composition according to claim 1, characterized in that the alkyl polyglycoside contains an average of from 1.2 to 1.5 saccharide units and a hydrocarbon group having from 10 to 16 carbon atoms.
  8. A dishwashing composition according to claim 1 or 7, characterized in that it comprises from 1 to 15 per cent by weight of alkyl polyglycoside.
  9. A dishwashing composition according to claim 1, characterized in that the anionic surface active agent is a water soluble sulfate or sulfonate.
  10. A dishwashing composition according to claim 1 or 9, characterized in that it comprises from 85 to 30 per cent by weight of anionic surface active agent.
EP92200679A 1991-04-09 1992-03-11 Liquid dishwashing composition Expired - Lifetime EP0508507B1 (en)

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
SE9101058A SE468252B (en) 1991-04-09 1991-04-09 LIQUID DISCHARGE COMPOSITION CONTAINING AN ANONICALLY SURFACTIVE AGENT AND A COMBINATION OF AMPOTATE SOCIETIES
SE9101058 1991-04-09

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EP0508507A1 true EP0508507A1 (en) 1992-10-14
EP0508507B1 EP0508507B1 (en) 1995-06-07

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Cited By (8)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
EP0543432A1 (en) * 1991-11-21 1993-05-26 Berol Nobel AB Liquid dishwashing composition
WO1996010558A1 (en) * 1994-10-04 1996-04-11 Henkel Kommanditgesellschaft Auf Aktien Pumpable aqueous tenside concentrates
EP0728836A3 (en) * 1995-02-23 1997-03-05 Goldschmidt Ag Th Storage stable, concentrated surfactant composition based on alkyl glycosides
EP0780464A2 (en) 1995-12-21 1997-06-25 Henkel Kommanditgesellschaft auf Aktien Process for the preparation of light-coloured, low-viscosity surfactant concentrates
US5883068A (en) * 1994-10-04 1999-03-16 Henkel Kommanditgesellschaft Auf Aktien Pumpable water-containing surfactant concentrates
US5932535A (en) * 1995-12-21 1999-08-03 Henkel Kommanditgesellschaft Auf Aktien Process for the production of light-colored, low-viscosity surfactant concentrates
EP1003605A1 (en) * 1997-06-12 2000-05-31 Henkel Corporation Use of alkyl polyglycosides to improve foam stabilization of amphoacetates
US6703427B2 (en) 1999-12-16 2004-03-09 Beiersdorf Ag Method of preparing particularly skin-compatible cosmetic or dermatological cleansing preparations

Families Citing this family (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
DE19960766A1 (en) * 1999-12-16 2001-06-21 Beiersdorf Ag Cosurfactant use to reduce binding of sodium lauryl ether sulfate to skin is useful in production of mildly washing-active cosmetic or dermatological formulation, e.g. shower or bath preparation, cleanser or shampoo

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Publication number Priority date Publication date Assignee Title
EP0250181A2 (en) * 1986-06-16 1987-12-23 Helene Curtis Industries, Inc. Mild detergent compositions
EP0280143A1 (en) * 1987-02-25 1988-08-31 Henkel Kommanditgesellschaft auf Aktien Liquid cleaning agent
EP0341071A2 (en) * 1988-05-06 1989-11-08 Unilever Plc Detergent compositions
EP0364744A1 (en) * 1988-09-20 1990-04-25 Kao Corporation Detergent composition

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JP2745071B2 (en) * 1989-09-29 1998-04-28 川研ファインケミカル株式会社 Liquid detergent composition

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Publication number Priority date Publication date Assignee Title
EP0250181A2 (en) * 1986-06-16 1987-12-23 Helene Curtis Industries, Inc. Mild detergent compositions
EP0280143A1 (en) * 1987-02-25 1988-08-31 Henkel Kommanditgesellschaft auf Aktien Liquid cleaning agent
EP0341071A2 (en) * 1988-05-06 1989-11-08 Unilever Plc Detergent compositions
EP0364744A1 (en) * 1988-09-20 1990-04-25 Kao Corporation Detergent composition

Non-Patent Citations (1)

* Cited by examiner, † Cited by third party
Title
J. PALICKA '2nd World Surfactants Congress proceedings , vol. III' 27 May 1988 , CESIO AND ASPA , PARIS *

Cited By (11)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
EP0543432A1 (en) * 1991-11-21 1993-05-26 Berol Nobel AB Liquid dishwashing composition
US5340502A (en) * 1991-11-21 1994-08-23 Berol Novel Ab Liquid dishwashing compositions comprising anionic tenside and three amphoteric compounds
WO1996010558A1 (en) * 1994-10-04 1996-04-11 Henkel Kommanditgesellschaft Auf Aktien Pumpable aqueous tenside concentrates
US5883068A (en) * 1994-10-04 1999-03-16 Henkel Kommanditgesellschaft Auf Aktien Pumpable water-containing surfactant concentrates
US5925747A (en) * 1994-10-04 1999-07-20 Henkel Kommanditgesellschaft Auf Aktien Pumpable water-containing surfactant concentrates
EP0728836A3 (en) * 1995-02-23 1997-03-05 Goldschmidt Ag Th Storage stable, concentrated surfactant composition based on alkyl glycosides
EP0780464A2 (en) 1995-12-21 1997-06-25 Henkel Kommanditgesellschaft auf Aktien Process for the preparation of light-coloured, low-viscosity surfactant concentrates
US5932535A (en) * 1995-12-21 1999-08-03 Henkel Kommanditgesellschaft Auf Aktien Process for the production of light-colored, low-viscosity surfactant concentrates
EP1003605A1 (en) * 1997-06-12 2000-05-31 Henkel Corporation Use of alkyl polyglycosides to improve foam stabilization of amphoacetates
EP1003605A4 (en) * 1997-06-12 2001-04-18 Henkel Corp Use of alkyl polyglycosides to improve foam stabilization of amphoacetates
US6703427B2 (en) 1999-12-16 2004-03-09 Beiersdorf Ag Method of preparing particularly skin-compatible cosmetic or dermatological cleansing preparations

Also Published As

Publication number Publication date
NO921369L (en) 1992-10-12
JPH05140587A (en) 1993-06-08
DK0508507T3 (en) 1995-10-09
EP0508507B1 (en) 1995-06-07
DE69202807T2 (en) 1995-10-19
JPH0765071B2 (en) 1995-07-12
SE9101058D0 (en) 1991-04-09
NO178898C (en) 1996-06-26
NO178898B (en) 1996-03-18
SE468252B (en) 1992-11-30
NO921369D0 (en) 1992-04-08
ATE123519T1 (en) 1995-06-15
SE9101058L (en) 1992-10-10
DE69202807D1 (en) 1995-07-13
ES2073238T3 (en) 1995-08-01

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