WO1992005236A1 - Liquid dishwashing composition - Google Patents

Liquid dishwashing composition Download PDF

Info

Publication number
WO1992005236A1
WO1992005236A1 PCT/SE1991/000257 SE9100257W WO9205236A1 WO 1992005236 A1 WO1992005236 A1 WO 1992005236A1 SE 9100257 W SE9100257 W SE 9100257W WO 9205236 A1 WO9205236 A1 WO 9205236A1
Authority
WO
WIPO (PCT)
Prior art keywords
compounds
amphoteric
group
formula
dishwashing composition
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.)
Ceased
Application number
PCT/SE1991/000257
Other languages
French (fr)
Inventor
Jadwiga Palicka
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
Nouryon Surface Chemistry AB
Original Assignee
Berol Nobel AB
Priority date (The priority date 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 date listed.)
Filing date
Publication date
Application filed by Berol Nobel AB filed Critical Berol Nobel AB
Priority to FI922184A priority Critical patent/FI922184L/en
Priority to DE69117726T priority patent/DE69117726T2/en
Priority to EP91910074A priority patent/EP0500819B1/en
Publication of WO1992005236A1 publication Critical patent/WO1992005236A1/en
Priority to NO921960A priority patent/NO179952C/en
Anticipated expiration legal-status Critical
Ceased legal-status Critical Current

Links

Classifications

    • CCHEMISTRY; METALLURGY
    • C11ANIMAL OR VEGETABLE OILS, FATS, FATTY SUBSTANCES OR WAXES; FATTY ACIDS THEREFROM; DETERGENTS; CANDLES
    • C11DDETERGENT COMPOSITIONS; USE OF SINGLE SUBSTANCES AS DETERGENTS; SOAP OR SOAP-MAKING; RESIN SOAPS; RECOVERY OF GLYCEROL
    • C11D3/00Other compounding ingredients of detergent compositions covered in group C11D1/00
    • C11D3/0005Other compounding ingredients characterised by their effect
    • C11D3/0094High foaming compositions
    • CCHEMISTRY; METALLURGY
    • C11ANIMAL OR VEGETABLE OILS, FATS, FATTY SUBSTANCES OR WAXES; FATTY ACIDS THEREFROM; DETERGENTS; CANDLES
    • C11DDETERGENT COMPOSITIONS; USE OF SINGLE SUBSTANCES AS DETERGENTS; SOAP OR SOAP-MAKING; RESIN SOAPS; RECOVERY OF GLYCEROL
    • C11D1/00Detergent compositions based essentially on surface-active compounds; Use of these compounds as a detergent
    • C11D1/88Ampholytes; Electroneutral compounds
    • 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
    • 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
    • C11D1/66Non-ionic compounds
    • C11D1/75Amino oxides

Definitions

  • Liquid dishwashing composition The present invention relates to liquid dishwashing compositions and • more particularly to such compositions which contain an anionic tenside, at least one amphoteric surface active compound and at least one foam boosting compoun .
  • the most common commercial liquid dishwashing com ⁇ positions are primarily intended for hand dishwashing and are as a rule aqueous solutions containing anionic ten- sides, such as al yl sulfonates and alkyl ether sulfates, as essential component.
  • anionic ten- sides such as al yl sulfonates and alkyl ether sulfates
  • These dishwashing agents are entirely satisfactory with regard to cleaning effect, foam forming effect and foam stability.
  • the dishwashing compositions based on this type of anionic surface active agents are not satisfactory from an environmental point of view nor with regard to mildness to skin, since they have a certain irritating and allergy causing effect.
  • anionic tensides such as for example paraffin sulfonates
  • anionic tensides in dishwashing compositions can be replaced by at least one amphoteric surface active compound and at least one foam boasting compound which is an amine oxide, an amido betaine or an amide to give a dishwashing composition which is mild and kind to the skin, has a good foam stability and gives a low biological load and is more efficient than a dishwashing composition based solely on anionic tensides.
  • 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.
  • amphoteric surface active compounds present in the dishwashing compositions of the invention can be characterized by the general formula (I) R - (A) n - [N - (CHRx J xl y - N - Q ( I )
  • R is a hydrocarbon group having from 7 to 22 carbon atoms
  • A is the group (C(O) )
  • n is 0 or 1
  • Ri is hydrogen or a lower alkyl group
  • x is 2 or 3
  • y is an integer of 0 to 4
  • Q is the group -R 2 COOM wherein R 2 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
  • B is hydrogen or a group Q as defined.
  • Amphoteric compounds encompassed by the above given formula 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. According to the European patent application 160507 a combination of two different amphoteric compounds en ⁇ compassed by the above given formula is used in mild shampoo 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 substi- tuents such as hydroxyl groups.
  • the group R can also contain one or several, up to about 20, ethylene oxide 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.
  • R- ⁇ 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 R 2 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 sub ⁇ stituted ammonium such as for example mono-, di- or tri- hydroxyethylammonium. M is preferably a sodium ion.
  • Preferred compounds of the formula (I) have the formula (II) :
  • Q is CH 2 -COOM or CH CH 2 COOM
  • y is 1, 2 or 3 and wherein M, R, x, A, n and B have the above given meanings.
  • 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.
  • amphoteric compound of type 1 acts primarily as a tenside and suds former and the amphoteric compound of type 2 acts primarily as a detoxifying tenside.
  • Suitable weight ratios between compounds of type 1 and type 2 is within the range of from 1:10 to 10:1 and preferably within the range of from 1:5 to 5:1.
  • amphoteric compounds of type 1 x in the above given formulae is suitably 2 and the groups B are hydrogen or groups Q.
  • amphoteric compounds of type 2 x in the above given formulae is suitably 3 and all groups B are groups Q.
  • amphoteric compounds containing a carbonyl group such compounds which can be characterized by the general formula (III)
  • R, A, y, Q and B have the same meaning as given for compounds of formula (I), whereby, however, one group B is the group -CH CHR*0H, wherein R * is H or CH 3 are used in combination with the amphoteric compound which does not contain a carbonyl group.
  • 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 l and Q is the group -CH 2 COOM.
  • Amphoteric compounds of formulae Ilia and Illb are commercially available as mixtures and usually with a weight ratio of compounds of formula Ilia to compounds of formula Illb within the range of 1:10 to 10:1. Like the amphoteric compounds of formula I and II which contain a carbonyl group the compounds of formula III, Ilia and Illb act primarily as tensides and suds formers. Suitable weight ratios between compounds of formula III or Ilia and/or Illb and amphoteric compounds which do not contain a carbonyl group is within the range of from 1:10 to 10:1 and prefer ⁇ ably within the range of from 1:5 to 5:1.
  • Amphoteric compounds of the above given formulae are commercially available and sold under the trade name Am ⁇ holak( R ) by Berol Nobel AB, Sweden.
  • amphoteric compounds can partly replace anionic tensides in liquid dishwashing compositions.
  • the amphoteric compounds are com ⁇ bined with an amide, an amido betaine or an amine oxide having this effect.
  • Amides, amido betaines and amine oxides with this effect for dishwashing agents and other products are per se known and can generally be characterized as amides, amido betaines and amine oxides respectively con ⁇ taining 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.
  • suitable amides can be mentioned ammonium and ethanol amides, such as mono- and diethanol amides of fatty acids containing at least one longer hydrophobic group having at least 7 carbon atoms.
  • the amides can be characterized by the general formula (IV) R - CO - N(H) p (R 1 0H) 2 _p (IV) wherein R is the longer hydrophobic hydrocarbon group, which suitably is a saturated or unsaturated, straight or branched, aliphatic hydrocarbon group with 7 to 21 carbon atoms and preferably is an alkyl or alkenyl group with from 11 to 17 carbon atoms.
  • R ⁇ is a methylene or ethylene group and p is 1 or 2.
  • suitable amides can be mentioned mono- and diethanol amides of natural or synthetic fatty acids having 12 to 18 carbon atoms, for example dodecyl carboxylic acid and coco fatty acid.
  • amido betaines which can be used can be charac ⁇ terized by the general formula (V)
  • R is the longer hydrophobic hydrocarbon group, which suitably is a saturated or unsaturated, straight or branched, aliphatic hydrocarbon group with 7 to 21 carbon atoms and preferably is an alkyl or alkenyl group with from 11 to 17 carbon atoms, n is 1 or 2 and M is preferably hydrogen or a sodium ion.
  • the amine oxides which can be used can be charac ⁇ terized by the formula (VI) R(R 1 ) 2 N- ) (VI) wherein R is the longer hydrophobic hydrocarbon group, suitably a saturated or unsaturated, straight or branched aliphatic hydrocarbon group having at least 8 carbon atoms.
  • R is especially a group having from 8 to 22 carbon atoms, and suitably it is an alkyl group which can be substituted by a hydroxyl group and also contain one or several, up to about 10, alkoxy groups, preferably ethylene oxide groups.
  • the groups R ⁇ are, independent of each other, lower alkyl or hydroxy alkyl groups with from 1 to 4 carbon atoms.
  • the amine oxides are preferred.
  • the group R is preferable a coconut alkyl group.
  • the weight ratio of the foam boosting compound or compounds, ie the amide, amido- betaine or amine oxide or mixture of two or more of these, to the amphoteric compound or compounds should suitably be at least l:10 and the ratio is suitably within the range of from 1:10 to 10:1 and preferably within the range from 1:5 to 5:1.
  • an amphoteric compound in combination with a fatty acid amide, an amido- betaine or an amine oxide having foam boosting and foam stabilizing effect anionic tensides, which normally are water soluble salts of organic sulfonated acid or sulfated alcohols, in liquid dishwashing compositions can be re ⁇ placed to a certain extent and hereby a dishwashing com ⁇ position is obtained which is advantageous from a biologi- cal point of view and advantageous with regard to mildness at use.
  • the improved mildness which is obtained is depen ⁇ dent on an efficient detoxification of anionic tensides through formation of mixed micelles of the anionic surface active compounds and the amphoteric surface active com- pounds.
  • anionic tensides of the above mentioned types are also present, but in lower amounts than usual.
  • the amount of anionic tenside is suitably within the range of from 90 to 20 per cent by weight, based on the total amount of amphoteric surface active compounds and anionic surface active compounds, preferably within the range 85 to 60 per cent and most preferably within the range of from 80 to 60 per cent by weight.
  • the anionic tensides are, as indicated above, water soluble salts of organic sulfonated acids or sulfated alcohols, 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.
  • 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 of these salts are alkali metals, alkaline earth metals, ammonium or amines such as mono-, di- and tri- ethanol 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 con ⁇ tains an average of from 11 to 13 carbon atoms.
  • 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 ampho ⁇ teric 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 con- ventional manner. Normal dosage is about 0.2 g/1 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 ampho ⁇ teric compounds can also be present if desired, such as betaines, and also nonionic tensides such as glycosides.
  • betaines such as betaines
  • nonionic tensides such as glycosides.
  • Dishwashing compositions were prepared from the following components (all amounts given are as 100% active substance) :
  • Composition I 12 g of linear alkyl benzene sulfonate with C12 to C18 alkyl groups, 7 g of sodium lauryl ether sulfate with 3 ethylene oxide groups, 2 g of C12-C18 alkane sul ⁇ fonate, 2 g of ethanol and 77 g of water.
  • This composition is a standard dishwashing composition.
  • Composition II 1.68 g of sodium lauryl ether sulfate with 3 ethylene oxide groups, 10.8 g of C12-C18 alkane sul ⁇ fonate, 2.22 g of amphoteric compounds, a 1:1 mixture of amphoteric compounds sold under the trade marks Ampholak ( R ) XCO-30 and Ampholak( R >7TX, respectively, 1.11 g of alkyl dimethyl amine oxide wherein the alkyl group had 14 carbon atoms and 84.19 g of water.
  • the first mentioned amphoteric compound can chemically be characterized as cocoamphocarboxyglycinate and contains a carbonyl group and comprises a mixture of compounds defined in formulae Ilia and Illb) and the other one can chemically be de ⁇ scribed as tallowampho polycarboxyglycinate, corresponds to formulae II and does not contain a carbonyl group.
  • composition II The efficiency of composition II according to the invention was set in relation to this and found to be 2.4.

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)
  • Magnetic Record Carriers (AREA)
  • Details Of Garments (AREA)

Abstract

Liquid dishwashing composition which contains at least one amphoteric surface active compound, at least one anionic tenside and at least one foam boosting amide, amidobetaine or amine oxide. The composition suitably contains a mixture of two amphoteric surface active compounds whereby one contains a carbonyl group and the other does not contain such a group. The amphoteric surface active compounds partly replace anionic tensides and hereby a dishwashing composition is obtained which is mild and satisfactory with regard to environment.

Description

Liquid dishwashing composition The present invention relates to liquid dishwashing compositions and more particularly to such compositions which contain an anionic tenside, at least one amphoteric surface active compound and at least one foam boosting compoun .
The most common commercial liquid dishwashing com¬ positions are primarily intended for hand dishwashing and are as a rule aqueous solutions containing anionic ten- sides, such as al yl 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 from an environmental point of view nor with regard to mildness to skin, since they have a certain irritating and allergy causing effect. For environ¬ mental reasons it has during the last few years been desired to decrease the total amount of anionic tensides, such as for example paraffin sulfonates, used in different cleaning purposes.
According to the present invention it has been found that anionic tensides in dishwashing compositions to a certain extent can be replaced by at least one amphoteric surface active compound and at least one foam boasting compound which is an amine oxide, an amido betaine or an amide to give a dishwashing composition which is mild and kind to the skin, has a good foam stability and gives a low biological load and is more efficient than a dishwashing composition based solely on anionic tensides.
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.
The amphoteric surface active compounds present in the dishwashing compositions of the invention can be characterized by the general formula (I) R - (A)n - [N - (CHRx J xl y - N - Q ( I )
wherein R is a hydrocarbon group having from 7 to 22 carbon atoms, A is the group (C(O) ) , n is 0 or 1, Ri 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 encompassed by the above given formula 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. According to the European patent application 160507 a combination of two different amphoteric compounds en¬ compassed by the above given formula is used in mild shampoo compositions.
In the amphoteric surface active compounds of the above given formula which are used in the present dishwash¬ ing 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 substi- tuents such as hydroxyl groups. The group R can also contain one or several, up to about 20, ethylene oxide 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. R-^ 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 sub¬ stituted ammonium such as for example mono-, di- or tri- hydroxyethylammonium. M is preferably a sodium ion.
Preferred compounds of the formula (I) have the formula (II) :
R - (A)n - [N - (CH2)χ]y - N - Q (II)
wherein Q is CH2-COOM or CH CH2COOM, y is 1, 2 or 3 and wherein M, R, x, A, n and B have the above given meanings. 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 it is particularly advantageous to use a combination of two amphoteric com¬ pounds encompassed by the formulae (I) and (II) whereby one compound contains a carbonyl group (below termed type 1) and the other does not contain such a group (below termed type 2) , ie an amphoteric compound wherein n is i and, respectively, an amphoteric compound wherein n is 0. The amphoteric compound of type 1 acts primarily as a tenside and suds former and the amphoteric compound of type 2 acts primarily as a detoxifying tenside. Suitable weight ratios between compounds of type 1 and type 2 is within the range of from 1:10 to 10:1 and preferably within the range of from 1:5 to 5:1. For amphoteric compounds of type 1 x in the above given formulae is suitably 2 and the groups B are hydrogen or groups Q. For amphoteric compounds of type 2 x in the above given formulae is suitably 3 and all groups B are groups Q.
According to another preferred embodiment of the present invention as amphoteric compounds containing a carbonyl group such compounds which can be characterized by the general formula (III)
R - A - [N - CH2CH2]y - N - Q (III)
wherein R, A, y, Q and B have the same meaning as given for compounds of formula (I), whereby, however, one group B is the group -CH CHR*0H, wherein R* is H or CH3 are used in combination with the amphoteric compound which does not contain a carbonyl group. 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 l and Q is the group -CH2COOM. As typical examples can be given compounds of formulae (Ilia) and/or (Illb)
R - A - N - CH2CH2 - N - CH2COOM (Ilia) and/or CH2CH2OH CH2COOM
R - A - N - CH2CH2 - N - CH2COOM (Illb) H CH2CH2OH
Amphoteric compounds of formulae Ilia and Illb are commercially available as mixtures and usually with a weight ratio of compounds of formula Ilia to compounds of formula Illb within the range of 1:10 to 10:1. Like the amphoteric compounds of formula I and II which contain a carbonyl group the compounds of formula III, Ilia and Illb act primarily as tensides and suds formers. Suitable weight ratios between compounds of formula III or Ilia and/or Illb and amphoteric compounds which do not contain a carbonyl group is within the range of from 1:10 to 10:1 and prefer¬ ably within the range of from 1:5 to 5:1.
Amphoteric compounds of the above given formulae are commercially available and sold under the trade name Amρholak(R) by Berol Nobel AB, Sweden.
According to the present invention it has been found that the above amphoteric compounds can partly replace anionic tensides in liquid dishwashing compositions. In order to obtain dishwashing compositions having sufficient- ly good foam stability the amphoteric compounds are com¬ bined with an amide, an amido betaine or an amine oxide having this effect. Amides, amido betaines and amine oxides with this effect for dishwashing agents and other products are per se known and can generally be characterized as amides, amido betaines and amine oxides respectively con¬ taining 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 examples of suitable amides can be mentioned ammonium and ethanol amides, such as mono- and diethanol amides of fatty acids containing at least one longer hydrophobic group having at least 7 carbon atoms. The amides can be characterized by the general formula (IV) R - CO - N(H)p(R10H)2_p (IV) wherein R is the longer hydrophobic hydrocarbon group, which suitably is a saturated or unsaturated, straight or branched, aliphatic hydrocarbon group with 7 to 21 carbon atoms and preferably is an alkyl or alkenyl group with from 11 to 17 carbon atoms. R± is a methylene or ethylene group and p is 1 or 2. As some specific examples of suitable amides can be mentioned mono- and diethanol amides of natural or synthetic fatty acids having 12 to 18 carbon atoms, for example dodecyl carboxylic acid and coco fatty acid.
The amido betaines which can be used can be charac¬ terized by the general formula (V)
R - 0 - NH - (CH2)3 - i +-(CH2)nCOOM (V)
wherein R is the longer hydrophobic hydrocarbon group, which suitably is a saturated or unsaturated, straight or branched, aliphatic hydrocarbon group with 7 to 21 carbon atoms and preferably is an alkyl or alkenyl group with from 11 to 17 carbon atoms, n is 1 or 2 and M is preferably hydrogen or a sodium ion.
The amine oxides which can be used can be charac¬ terized by the formula (VI) R(R1)2N- ) (VI) wherein R is the longer hydrophobic hydrocarbon group, suitably a saturated or unsaturated, straight or branched aliphatic hydrocarbon group having at least 8 carbon atoms. R is especially a group having from 8 to 22 carbon atoms, and suitably it is an alkyl group which can be substituted by a hydroxyl group and also contain one or several, up to about 10, alkoxy groups, preferably ethylene oxide groups. The groups R^ are, independent of each other, lower alkyl or hydroxy alkyl groups with from 1 to 4 carbon atoms. Of the mentioned foam boosting compounds the amine oxides are preferred. In the foam boosting compounds the group R is preferable a coconut alkyl group. The weight ratio of the foam boosting compound or compounds, ie the amide, amido- betaine or amine oxide or mixture of two or more of these, to the amphoteric compound or compounds should suitably be at least l:10 and the ratio is suitably within the range of from 1:10 to 10:1 and preferably within the range from 1:5 to 5:1.
By using at least one amphoteric compound, as above defined, in combination with a fatty acid amide, an amido- betaine or an amine oxide having foam boosting and foam stabilizing effect anionic tensides, which normally are water soluble salts of organic sulfonated acid or sulfated alcohols, in liquid dishwashing compositions can be re¬ placed to a certain extent and hereby a dishwashing com¬ position is obtained which is advantageous from a biologi- cal point of view and advantageous with regard to mildness at use. The improved mildness which is obtained is depen¬ dent on an efficient detoxification of anionic tensides through formation of mixed micelles of the anionic surface active compounds and the amphoteric surface active com- pounds. The very low critical micelle concentration of the specific amphoteric compounds is hereby utilized. The desired effect is thus obtained with very small amounts of amphoteric compound, particularly of those of type 2. Dish¬ washing compositions according to the present invention have also been found to be as effective as such based on solely anionic tensides and this also with regard to economy.
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 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 90 to 20 per cent by weight, based on the total amount of amphoteric surface active compounds and anionic surface active compounds, preferably within the range 85 to 60 per cent and most preferably within the range of from 80 to 60 per cent by weight. The anionic tensides are, as indicated above, water soluble salts of organic sulfonated acids or sulfated alcohols, 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 of these salts are alkali metals, alkaline earth metals, ammonium or amines such as mono-, di- and tri- ethanol 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 con¬ tains an average of from 11 to 13 carbon atoms.
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 ampho¬ teric 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 con- ventional manner. Normal dosage is about 0.2 g/1 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 ampho¬ teric compounds can also be present if desired, such as betaines, and also nonionic tensides such as glycosides. As example of a complete dishwashing composition according to the invention as concerns main components those listed below can be given, wherein the ratios of anionic surface active agents to amphoteric surface active agents and ratios for "oam boosting compound are adjusted to fall within the above given limits: Amphoteric compounds as defined in formulae 1 - 10 % by weight Anionic tensid 10 - 20 % by weight
Amine oxide, amido- betaine or amide 0.3 - 3 % by weight Alcohol 0.5 - 2 % j weight
Water to 100 per cent by weight
The
Figure imgf000010_0001
..ition 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
Dishwashing compositions were prepared from the following components (all amounts given are as 100% active substance) :
Composition I: 12 g of linear alkyl benzene sulfonate with C12 to C18 alkyl groups, 7 g of sodium lauryl ether sulfate with 3 ethylene oxide groups, 2 g of C12-C18 alkane sul¬ fonate, 2 g of ethanol and 77 g of water. This composition is a standard dishwashing composition.
Composition II: 1.68 g of sodium lauryl ether sulfate with 3 ethylene oxide groups, 10.8 g of C12-C18 alkane sul¬ fonate, 2.22 g of amphoteric compounds, a 1:1 mixture of amphoteric compounds sold under the trade marks Ampholak (R) XCO-30 and Ampholak(R>7TX, respectively, 1.11 g of alkyl dimethyl amine oxide wherein the alkyl group had 14 carbon atoms and 84.19 g of water. The first mentioned amphoteric compound can chemically be characterized as cocoamphocarboxyglycinate and contains a carbonyl group and comprises a mixture of compounds defined in formulae Ilia and Illb) and the other one can chemically be de¬ scribed as tallowampho polycarboxyglycinate, corresponds to formulae II and does not contain a carbonyl group.
The two compositions were tested by titration of 2 g/1 of the solutions with bechamel sauce. Foam heights were determined and plotted against the amount of bechamel sauce. The areas of the diagrams were integrated and weighed and presented as efficiency versus content of amphoteric compound. The area for composition I, the reference, was set as efficiency 1. The efficiency of composition II according to the invention was set in relation to this and found to be 2.4.

Claims

Claims 1. Liquid dishwashing composition, characterized in that it comprises- a) at least one amphoteric compound having the general formula (I)
R - (A)n - [N - (CHR- xJy - N - Q (I)
wherein R is a hydrocarbon group having from 7 to 22 carbon atoms, A is the group (C(O)), n is 0 or 1, R-^ 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 groups Q as defined, b) a foam boosting compound which is an amide, an amido- betaine or an amine oxide, containing at least one longer hydrophobic hydrocarbon group having at least 7 carbon atoms, c) an anionic surface active agent, whereby the ratio of foam boosting compound to amphoteric compound is at least 1:10 and whereby the amount of anionic surface active agent is at the most 90 per cent by weight based on the total amount of amphoteric and anionic surface active compounds.
2. A dishwashing composition according to claim 1, characterized in that the amphoteric compound or compounds have the general formula (II) R - (A)n - [N - (CH2)χ]y - N - Q (II)
wherein y is 1, 2 or 3, R is a hydrocarbon group having from 7 to 22 carbon atoms, A is the group (C(0) ) , n is 0 or 1, i is hydrogen or a lower alkyl group, x is 2 or 3, y is 1, 2 or 3, Q is CH2-COOM or CH2CH2-C00M, M is hydrogen or an ion from the groups alkali metals, alkaline earth metals, ammonium or substituted ammonium and B is hydrogen or a group Q as defined.
3. Dishwashing composition according to claim 1 or 2, characterized in that it as amphoteric compounds com¬ prises a mixture of compounds of formula I or II in which n is 1 and compounds of formula I or II in which n is 0.
4. Dishwashing composition according to claim 1 or 2, characterized in that it as amphoteric compounds comprises a mixture of compounds of formula I or in which n is 0 and amphoteric compounds of the general formula
R - A (Ilia) and/or
Figure imgf000013_0001
R - A - N - CH2CH2 - N - CH2COOM (Illb) H CH2CH2OH wherein R, A and M have the same meanings as above defined for amphoteric compounds of formula (I) and (II).
5. Dishwashing compositions according to claim 3 or 4, characterized in that the weight ratio in the mixture of compounds of formula. I or II in which n is 1 and such of formula I or II in which n is 0 or the weight ratio in the mixture of compounds of formula Ilia and/or Illb to compounds of formula I or II in which n is 0 is within the range of from 1:10 to 10:l.
6. Dishwashing composition according to any of the preceding claims, characterized in that R in the amphoteric compounds is an alkyl or alkenyl group having from 12 to 22 carbon atoms.
7. Dishwashing composition .according to any of the preceding claims, characterized in that it comprises amphoteric compounds of formula I or II wherein n is 0 and all groups B are groups Q.
8. Dishwashing composition according to claim 1, characterized in that the foam boosting compound is an amine oxide.
9. Dishwashing composition according to claim 1, characterized in that the anionic surface active agent is a water soluble salt of an organic sulfonated acid or sul- fated alcohol.
10. Dishwashing composition according to claim 1 or 9, characterized in that the amount of anionic surface active agent is within the range of from 90 to 20 per cent by weight, based on the total amount of amphoteric and anionic surface active compounds.
PCT/SE1991/000257 1990-09-19 1991-04-09 Liquid dishwashing composition Ceased WO1992005236A1 (en)

Priority Applications (4)

Application Number Priority Date Filing Date Title
FI922184A FI922184L (en) 1990-09-19 1991-04-09 FLYTANDE DISKMEDELSKOMPOSITION.
DE69117726T DE69117726T2 (en) 1990-09-19 1991-04-09 COMPOSITION OF LIQUID DISHWASHER
EP91910074A EP0500819B1 (en) 1990-09-19 1991-04-09 Liquid dishwashing composition
NO921960A NO179952C (en) 1990-09-19 1992-05-18 Liquid detergent mixture

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
SE9002986A SE9002986D0 (en) 1990-09-19 1990-09-19 LIQUID DISC MEDIUM COMPOSITION
SE9002986-9 1990-09-19

Publications (1)

Publication Number Publication Date
WO1992005236A1 true WO1992005236A1 (en) 1992-04-02

Family

ID=20380401

Family Applications (1)

Application Number Title Priority Date Filing Date
PCT/SE1991/000257 Ceased WO1992005236A1 (en) 1990-09-19 1991-04-09 Liquid dishwashing composition

Country Status (11)

Country Link
EP (1) EP0500819B1 (en)
JP (1) JPH05502265A (en)
AT (1) ATE135038T1 (en)
AU (1) AU7903291A (en)
DE (1) DE69117726T2 (en)
DK (1) DK0500819T3 (en)
ES (1) ES2084165T3 (en)
FI (1) FI922184L (en)
NO (1) NO179952C (en)
SE (1) SE9002986D0 (en)
WO (1) WO1992005236A1 (en)

Cited By (6)

* 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
WO1994005752A3 (en) * 1992-09-01 1994-04-14 Procter & Gamble Liquid or gel dishwashing detergent composition containing alkyl amphocarboxylic acid and magnesium or calcium ions
WO1994011476A1 (en) * 1992-11-11 1994-05-26 Berol Nobel Ab Liquid dishwashing-detergent composition
WO1995001153A1 (en) * 1993-06-30 1995-01-12 Berol Nobel Ab Shampoo compositions
US5801139A (en) * 1997-06-05 1998-09-01 Lever Brothers Company, Division Of Conopco, Inc. Process for making bar compositions comprising novel chelating surfactants
US5869441A (en) * 1997-06-05 1999-02-09 Lever Brothers Company, Division Of Conopco, Inc. Bar compositions comprising novel chelating surfactants

Families Citing this family (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
FR2913351B1 (en) 2007-03-08 2010-11-26 Rhodia Recherches Et Tech USE OF BETAINE AS A DRAINAGE REDUCTION AGENT FOR FOAM

Citations (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
EP0214868A2 (en) * 1985-09-10 1987-03-18 Berol Nobel Ab Surfactants for use in cleaning compositions
EP0269939A2 (en) * 1986-11-18 1988-06-08 Kao Corporation Detergent composition

Patent Citations (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
EP0214868A2 (en) * 1985-09-10 1987-03-18 Berol Nobel Ab Surfactants for use in cleaning compositions
EP0269939A2 (en) * 1986-11-18 1988-06-08 Kao Corporation Detergent composition

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
US5340502A (en) * 1991-11-21 1994-08-23 Berol Novel Ab Liquid dishwashing compositions comprising anionic tenside and three amphoteric compounds
WO1994005752A3 (en) * 1992-09-01 1994-04-14 Procter & Gamble Liquid or gel dishwashing detergent composition containing alkyl amphocarboxylic acid and magnesium or calcium ions
WO1994011476A1 (en) * 1992-11-11 1994-05-26 Berol Nobel Ab Liquid dishwashing-detergent composition
US5589447A (en) * 1992-11-11 1996-12-31 Berol Nobel Ab Liquid dishwashing-detergent composition
WO1995001153A1 (en) * 1993-06-30 1995-01-12 Berol Nobel Ab Shampoo compositions
US5801139A (en) * 1997-06-05 1998-09-01 Lever Brothers Company, Division Of Conopco, Inc. Process for making bar compositions comprising novel chelating surfactants
US5869441A (en) * 1997-06-05 1999-02-09 Lever Brothers Company, Division Of Conopco, Inc. Bar compositions comprising novel chelating surfactants

Also Published As

Publication number Publication date
NO921960L (en) 1992-07-20
NO921960D0 (en) 1992-05-18
JPH05502265A (en) 1993-04-22
NO179952B (en) 1996-10-07
DE69117726D1 (en) 1996-04-11
SE9002986D0 (en) 1990-09-19
FI922184A7 (en) 1992-05-13
FI922184A0 (en) 1992-05-13
AU7903291A (en) 1992-04-15
ATE135038T1 (en) 1996-03-15
FI922184L (en) 1992-05-13
ES2084165T3 (en) 1996-05-01
NO179952C (en) 1997-01-15
EP0500819A1 (en) 1992-09-02
DK0500819T3 (en) 1996-06-24
EP0500819B1 (en) 1996-03-06
DE69117726T2 (en) 1996-07-18

Similar Documents

Publication Publication Date Title
EP0214868B1 (en) Surfactants for use in cleaning compositions
AU2010347222B2 (en) Sulfomethylsuccinates, process for making same and compositions containing same
DE602004007012T2 (en) LIQUID DISHWASHER
AU654508B2 (en) Concentrated liquid detergent composition containing alkyl benzene sulfonate and magnesium
CH657372A5 (en) STABILIZED ENZYME-LIQUID CLEANER.
US4992263A (en) Thickended aqueous surfactant solutions and their use in cosmetic preparations
DE69319385T2 (en) Liquid cleaning agent based on highly foaming, non-ionic, surface-active agents
EP0500819B1 (en) Liquid dishwashing composition
JPH0441718B2 (en)
EP0508507B1 (en) Liquid dishwashing composition
CA1209438A (en) Surfactant
US5589447A (en) Liquid dishwashing-detergent composition
US5340502A (en) Liquid dishwashing compositions comprising anionic tenside and three amphoteric compounds
CA1210662A (en) Anionic nonionic surfactant mixture
JP3730752B2 (en) Liquid detergent composition
DE60034215T2 (en) SURFACE ACTIVE COMPOSITION
DE69401066T2 (en) LIQUID CLEANING AGENT BASED ON HIGH-FOAMING, NON-IONIC, SURFACE-ACTIVE AGENTS
JPH02105894A (en) Detergent composition
WO1999049007A1 (en) Washing up liquid containing fatty acid oligo alkylene glycol ester sulphates
GB2290301A (en) Detergent Formulation
KR19990066570A (en) Liquid detergent composition for concentrated kitchen
KR940014758A (en) Liquid detergent composition

Legal Events

Date Code Title Description
AK Designated states

Kind code of ref document: A1

Designated state(s): AU CA FI JP NO US

AL Designated countries for regional patents

Kind code of ref document: A1

Designated state(s): AT BE CH DE DK ES FR GB GR IT LU NL SE

WWE Wipo information: entry into national phase

Ref document number: 1991910074

Country of ref document: EP

WWE Wipo information: entry into national phase

Ref document number: 922184

Country of ref document: FI

WWP Wipo information: published in national office

Ref document number: 1991910074

Country of ref document: EP

NENP Non-entry into the national phase

Ref country code: CA

WWG Wipo information: grant in national office

Ref document number: 1991910074

Country of ref document: EP