EP0616026A1 - Concentrated cleaning compositions - Google Patents

Concentrated cleaning compositions Download PDF

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Publication number
EP0616026A1
EP0616026A1 EP93870125A EP93870125A EP0616026A1 EP 0616026 A1 EP0616026 A1 EP 0616026A1 EP 93870125 A EP93870125 A EP 93870125A EP 93870125 A EP93870125 A EP 93870125A EP 0616026 A1 EP0616026 A1 EP 0616026A1
Authority
EP
European Patent Office
Prior art keywords
alkyl
surfactant
mixtures
chain
composition according
Prior art date
Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
Withdrawn
Application number
EP93870125A
Other languages
German (de)
French (fr)
Inventor
Marc François Theophile Evers
Massimo Morini
Louise Gail Scott
Peter Rosalia Joannes Geboes
Vincent Reniers
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.)
Procter and Gamble Co
Original Assignee
Procter and Gamble Co
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
Priority claimed from EP93870050A external-priority patent/EP0616028A1/en
Application filed by Procter and Gamble Co filed Critical Procter and Gamble Co
Priority to EP93870125A priority Critical patent/EP0616026A1/en
Priority to PCT/US1994/002747 priority patent/WO1994021767A1/en
Priority to AU64073/94A priority patent/AU6407394A/en
Priority to CA 2158542 priority patent/CA2158542A1/en
Priority to CN 94192052 priority patent/CN1122611A/en
Priority to JP6521160A priority patent/JPH08508765A/en
Priority to NZ263393A priority patent/NZ263393A/en
Priority to BR9406013A priority patent/BR9406013A/en
Priority to MA23446A priority patent/MA23138A1/en
Priority to MA23445A priority patent/MA23137A1/en
Publication of EP0616026A1 publication Critical patent/EP0616026A1/en
Priority to NO953644A priority patent/NO953644D0/en
Priority to FI954396A priority patent/FI954396A/en
Withdrawn legal-status Critical Current

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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
    • C11D3/16Organic compounds
    • C11D3/20Organic compounds containing oxygen
    • C11D3/2075Carboxylic acids-salts thereof
    • C11D3/2079Monocarboxylic acids-salts thereof
    • 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
    • C11D1/02Anionic compounds
    • C11D1/12Sulfonic acids or sulfuric acid esters; Salts thereof
    • C11D1/14Sulfonic acids or sulfuric acid esters; Salts thereof derived from aliphatic hydrocarbons or mono-alcohols
    • C11D1/146Sulfuric acid esters
    • 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
    • C11D1/72Ethers of polyoxyalkylene glycols
    • 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
    • C11D1/825Mixtures of compounds all of which are non-ionic
    • C11D1/8255Mixtures of compounds all of which are non-ionic containing a combination of compounds differently alcoxylised or with differently alkylated chains
    • 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
    • C11D1/83Mixtures of non-ionic with anionic 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
    • C11D1/83Mixtures of non-ionic with anionic compounds
    • C11D1/831Mixtures of non-ionic with anionic compounds of sulfonates with ethers of polyoxyalkylenes without phosphates
    • 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
    • C11D3/02Inorganic compounds ; Elemental compounds
    • C11D3/04Water-soluble compounds
    • C11D3/10Carbonates ; Bicarbonates
    • 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
    • C11D3/16Organic compounds
    • C11D3/20Organic compounds containing oxygen
    • C11D3/2068Ethers
    • 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
    • C11D1/02Anionic compounds
    • C11D1/12Sulfonic acids or sulfuric acid esters; Salts thereof
    • C11D1/14Sulfonic acids or sulfuric acid esters; Salts thereof derived from aliphatic hydrocarbons or mono-alcohols
    • C11D1/143Sulfonic acid esters
    • 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
    • C11D1/722Ethers of polyoxyalkylene glycols having mixed oxyalkylene groups; Polyalkoxylated fatty alcohols or polyalkoxylated alkylaryl alcohols with mixed oxyalkylele groups

Definitions

  • the present invention relates to concentrated cleaning compositions. Although the present invention relates primarily to cleaning compositions for hard surfaces, it may also be of interest for other cleaning compositions including dishwashing and laundry detergent compositions.
  • Concentrated cleaning compositions are well known in the art. Concentrated compositions are mainly characterized by the fact that they comprise a higher concentration of active ingredients compared to a conventional cleaning composition, and a problem which is typically encountered when formulating concentrated cleaning compositions is therefore the physical stability of such compositions. Indeed, because such compositions comprise a high amount of active ingredients in a limited amount of water, stability problems appear which lead, if not solved, to compositions which separate into several phases. This phenomenon affects the performance of the composition and is visually noticeable, thereby rendering such formulations unfit for commercialization.
  • EP 316 726 discloses concentrated compositions in the form of microemulsions which comprise water, perfume, a surfactant and a so-called co-surfactant.
  • the co-surfactant is said to reduce the interfacial tension at interfaces between dispersed and continuous phases of an emulsion of said surfactant, thereby creating a stable microemulsion.
  • the so-called co-surfactants in the '726 publication are listed as specific glycol ethers, which are traditionally regarded as solvents in this field, or specific carboxylic acids.
  • the co-surfactants in the '726 publication do not appear to participate to the overall cleaning performance of the product.
  • a concentrated aqueous composition comprising a traditional long-chain surfactant, in combination with at least one short chain surfactant, i.e. with a hydrophobic group consisting of a C6-C10 alkyl chain.
  • Said short chain surfactants provide stability to the compositions herein and, in the same time, significantly boost the overall cleaning performance, especially grease cleaning, both in neat and dilute usage.
  • compositions herein are stable clear concentrated cleaning compositions comprising from 10 % to 80 % by weight of the total composition of water, less than 15 % perfume and at least one long chain surfactant comprising a C11- C24 alkyl chain as its hydrophobic portion, or mixtures thereof, said compositions further comprising at least one co-surfactant consisting of a short chain surfactant comprising a C6-C10 alkyl chain as its hydrophobic portion, or mixtures thereof, except where said short chain surfactant is an alkyl ether carboxylate, said alkyl chain as said hydrophobic portion is a C6-C8 alkyl chain.
  • compositions of the present invention are concentrated aqueous compositions.
  • concentrated it is meant herein that the compositions comprise from 10 % to 80 % by weight of the total composition of water, preferably from 15 % to 75 %, most preferably from 30 % to 75 %.
  • compositions according to the present invention are clear and stable.
  • clear and stable it is meant herein that the compositions of the present invention are macroscopically substantially transparent, in the absence of any opacifier, and that said compositions do not macroscopically separate into separate phases during at least 1 month, at temperatures ranging from 4°C to 50°C, upon standing.
  • compositions according to the present invention further comprise a long chain surfactant, or mixtures thereof.
  • All surfactants have in common that they comprise a hydrophobic portion and a hydrophilic portion.
  • long chain surfactants it is meant herein surfactants which comprise a C11 to C24 alkyl chain as their hydrophobic portion.
  • Such long chain surfactants are accordingly those conventionally used in this field and can be of any type.
  • suitable long chain surfactants for use herein include C11-C24 alkyl sulfates (C11-C24SO4), alkyl ether sulfates (C11-C24(OCH2CH2)eSO4), alkyl sulfonates (C11-C24SO3), alkyl succinates (C11-C24OOCCH2CH2COOZ), alkyl carboxylates (C11-C24COOM), alkyl ether carboxylates (C11-C24(OCH2CH2) e COOM), alkyl sarcosinates (C11-C24CON(CH3)R), alkyl sulfo succinates (C11-C24OOCCH(SO3M)CH2COOZ), amine oxides (C11-C24RR'NO), glucose amides (C11-C24CONR''X), alkyl pyrrolidones (C11-C24(C4H6ON), alkylpolylenes
  • e and p are independently from 0 to 20 and e+p>0
  • Z is M or R
  • M is H or any counterion such as those known in the art, including Na, K, Li, NH4, amine
  • X is a polyhydroxyhydrocarbyl having a linear hydrocarbyl chain with at least 3 hydroxyls directly connected to the chain, or an alkoxylated derivative thereof
  • R, R and R''' are C1-C5 alkyl groups, possibly functionalized with hydroxyl groups
  • R and R' are preferably C1-C3, most preferably methyl
  • R'' is preferably 2-hydroxyethyl or 2 hydroxypropyl
  • G is a saccharide, preferably glucose, and g is of from 1.5 to 8.
  • compositions according to the present invention may comprise any of the above surfactants alone, or any combination thereof, depending on the end use envisioned.
  • preferred long chain surfactants are selected from long chain alkyl sulfonates and long chain alkyl ethoxylates, and mixtures thereof.
  • compositions according to the present invention further comprise at least one short chain surfactant, or mixtures thereof.
  • short chain surfactants is as above for long chain surfactants, except that said alkyl group as said hydrophobic portion is a C6 to C10 alkyl group, and where said short chain surfactant is an alkyl ether carboxylate, said alkyl chain in said hydrophobic portion is a C6-C8 alkyl chain.
  • suitable short chain surfactants for use herein include those listed herein above in the description of long chain surfactants, but with shorter alkyl chain.
  • Preferred short chain nonionic surfactants for use herein are alkyl alkoxylates according to the formula C6-C10(OCH2CH2) e (OCH2CH2CH2) p OH, where e and p representing respectively the degree of ethoxylation and propoxylation are independently of from 0 to 20, and that e+p>0 .
  • Most preferred short chain nonionic surfactants for use herein are those where e and p are such that e+p is from 3 to 10, particularly those where p is 0 and e is from 3 to 8.
  • most preferred short chain nonionic surfactants for use herein are those where said short chain is a hydrocarbon chain comprising from 7 to 10 carbon atoms.
  • Said preferred short chain nonionic surfactants for use herein can be manufactured by the processes well known to the man skilled in the art, such as condensation of the corresponding alcohol and alkylene oxide, but such short chain surfactants are more conveniently commercially available for instance from Sidobre under the trade name Mergital @ C4 (C8EO4), from Kolb under the trade names Imbentin @ AG/810/050 and AG/810/080 (respectively C8-10EO5 and C8-10EO8).
  • Preferred short chain anionic surfactants for use herein are C6-C10 alkyl sulfates (C6-C10SO4) and alkyl sulfonates (C6-C10SO3). Most preferred are the C6-C8 alkyl sulfates and sulfonates.
  • Such short chain anionic surfactants can be made by well known sulphation or sulphonation processes followed by neutralization, but said anionic short chain surfactants are more conveniently commercially available, for instance from Rhone Poulenc under the trade name Rhodapon @ OLS, or from Witco under the trade name Witconate @ .
  • compositions according to the present invention may comprise from 0.1 % to 50 % by weight of the total composition, preferably from 1% to 40%, most preferably from 1.5% to 30% of said short chain surfactants.
  • the short chain surfactants herein act not only as active cleaning ingredients, but also as stabilizers. If short chain anionic surfactants are used, it is preferred to observe a minimum weight ratio of short chain anionic surfactant to longer chain surfactant of 1:10. If short chain nonionic surfactants are used, it is preferred to observe a minimum weight ratio of short chain nonionic to longer chain surfactant of 1:5.
  • compositions herein may further comprise a variety of other optional ingredients including builders, alkanolamines, pH adjusting agents, perfumes in amounts of less than 15% by weight of the total composition, dyes, bleaches, enzymes and the like.
  • a suds suppressing system in the compositions herein.
  • Said suds suppressing system can advantageously be a mixture of 2-alkyl alkanols as described for instance in DE 40 21 265, or mixtures thereof, with a C8 to C22 fatty acid, or mixtures thereof.
  • Such a system is particularly advantageous as both ingredients appear to act in synergy. Thus even a very low amount of said system is enough to control suds efficiently. Accordingly, said system is present in amounts of from 0.1% to 5% by weight of the total composition, preferably 0.5% to 3%.
  • compositions herein do not require the presence of a stabilizing compound.
  • stabilizing compound it is meant herein a compound whose sole function is to enhance the physical stability of the composition.
  • Such compounds are typically xylene or toluene sulphonate salts, and glycol ethers, including ethylene glycol monobutyl ether, diethylene glycol monobutyl ether, dipropylene glycol monobutyl ether, dipropylene glycol methyl ether, propylene glycol methyl ether, tripropylene glycol methyl ether, propylene glycol monobutyl ether and other various solvents suvh as ethanol and butanol. Accordingly, the compositions of the present invention are preferably substantially free of such stabilizing compounds.
  • the present invention further encompasses a method of cleaning a hard surface which comprises the steps of diluting a composition according to the preceding claims in water, then applying it to said hard surface.
  • a method of cleaning a hard surface which comprises the steps of diluting a composition according to the preceding claims in water, then applying it to said hard surface.
  • the compositions herein may be used both neat and diluted from 10 to 500 times.
  • compositions were evaluated for their physical stability at 4°C, at room temperature (20°C), and at 50°C.
  • Composition I which is not within the invention, was a gel at 4°C, and an emulsion at room temperature and at 50°C. All other compositions, within the invention, were clear transparent liquids in the same conditions.
  • compositions were made by mixing the listed ingredients in the listed proportions.

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  • Engineering & Computer Science (AREA)
  • Chemical Kinetics & Catalysis (AREA)
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Abstract

Stable and clear concentrated cleaning compositions are disclosed which comprise at least one long chain surfactant, and which are stabilized by the additional presence of short chain surfactants. The short chain surfactants further boost grease cleaning performance.

Description

    Technical Field
  • The present invention relates to concentrated cleaning compositions. Although the present invention relates primarily to cleaning compositions for hard surfaces, it may also be of interest for other cleaning compositions including dishwashing and laundry detergent compositions.
  • Background of the Invention
  • Concentrated cleaning compositions are well known in the art. Concentrated compositions are mainly characterized by the fact that they comprise a higher concentration of active ingredients compared to a conventional cleaning composition, and a problem which is typically encountered when formulating concentrated cleaning compositions is therefore the physical stability of such compositions. Indeed, because such compositions comprise a high amount of active ingredients in a limited amount of water, stability problems appear which lead, if not solved, to compositions which separate into several phases. This phenomenon affects the performance of the composition and is visually noticeable, thereby rendering such formulations unfit for commercialization.
  • Various solutions have been proposed to solve this problem which typically involve the use of specific stabilizing ingredients, or hydrotropes. Such ingredients have the sole function of stabilizing the composition. They thus increase the cost of formulating such compositions without providing any cleaning performance benefits, and they furthermore require to free up parts in the formulation which could otherwise be used to formulate more actives.
  • For instance, EP 316 726 discloses concentrated compositions in the form of microemulsions which comprise water, perfume, a surfactant and a so-called co-surfactant. The co-surfactant is said to reduce the interfacial tension at interfaces between dispersed and continuous phases of an emulsion of said surfactant, thereby creating a stable microemulsion. The so-called co-surfactants in the '726 publication are listed as specific glycol ethers, which are traditionally regarded as solvents in this field, or specific carboxylic acids. The co-surfactants in the '726 publication do not appear to participate to the overall cleaning performance of the product.
  • It is therefore an object of the present invention to formulate a stable concentrated cleaning composition without using ingredients which are provided for the sole purpose of providing stability to the compositions herein, but which also participate significantly to the cleaning performance of said compositions.
  • It has now been found that this object can be met by formulating a concentrated aqueous composition comprising a traditional long-chain surfactant, in combination with at least one short chain surfactant, i.e. with a hydrophobic group consisting of a C₆-C₁₀ alkyl chain. Said short chain surfactants provide stability to the compositions herein and, in the same time, significantly boost the overall cleaning performance, especially grease cleaning, both in neat and dilute usage.
  • Summary of the Invention
  • The compositions herein are stable clear concentrated cleaning compositions comprising from 10 % to 80 % by weight of the total composition of water, less than 15 % perfume and at least one long chain surfactant comprising a C₁₁- C₂₄ alkyl chain as its hydrophobic portion, or mixtures thereof, said compositions further comprising at least one co-surfactant consisting of a short chain surfactant comprising a C₆-C₁₀ alkyl chain as its hydrophobic portion, or mixtures thereof, except where said short chain surfactant is an alkyl ether carboxylate, said alkyl chain as said hydrophobic portion is a C₆-C₈ alkyl chain.
  • Detailed Description of the Invention
  • The compositions of the present invention are concentrated aqueous compositions. By concentrated, it is meant herein that the compositions comprise from 10 % to 80 % by weight of the total composition of water, preferably from 15 % to 75 %, most preferably from 30 % to 75 %.
  • The compositions according to the present invention are clear and stable. By clear and stable, it is meant herein that the compositions of the present invention are macroscopically substantially transparent, in the absence of any opacifier, and that said compositions do not macroscopically separate into separate phases during at least 1 month, at temperatures ranging from 4°C to 50°C, upon standing.
  • The compositions according to the present invention further comprise a long chain surfactant, or mixtures thereof. All surfactants have in common that they comprise a hydrophobic portion and a hydrophilic portion. By long chain surfactants, it is meant herein surfactants which comprise a C₁₁ to C₂₄ alkyl chain as their hydrophobic portion. Such long chain surfactants are accordingly those conventionally used in this field and can be of any type. Accordingly, suitable long chain surfactants for use herein include C₁₁-C₂₄ alkyl sulfates (C₁₁-C₂₄SO₄), alkyl ether sulfates (C₁₁-C₂₄(OCH₂CH₂)eSO₄), alkyl sulfonates (C₁₁-C₂₄SO₃), alkyl succinates (C₁₁-C₂₄OOCCH₂CH₂COOZ), alkyl carboxylates (C₁₁-C₂₄COOM), alkyl ether carboxylates (C₁₁-C₂₄(OCH₂CH₂)eCOOM), alkyl sarcosinates (C₁₁-C₂₄CON(CH₃)R), alkyl sulfo succinates (C₁₁-C₂₄OOCCH(SO₃M)CH₂COOZ), amine oxides (C₁₁-C₂₄RR'NO), glucose amides (C₁₁-C₂₄CONR''X), alkyl pyrrolidones (C₁₁-C₂₄(C₄H₆ON), alkylpolysaccharides (C₁₁-C₂₄OGg), alkyl alkoxylates (C₁₁₋ C₂₄(OCH₂CH₂)e(OCH₂CH₂CH₂)pOH) and betaines (C₁₁-C₂₄N⁺(CH₃)₂CH₂COO-). In the formulae in brackets, e and p are independently from 0 to 20 and e+p>0
    Figure imgb0001
    , Z is M or R, M is H or any counterion such as those known in the art, including Na, K, Li, NH₄, amine, X is a polyhydroxyhydrocarbyl having a linear hydrocarbyl chain with at least 3 hydroxyls directly connected to the chain, or an alkoxylated derivative thereof, R, R and R''' are C₁-C₅ alkyl groups, possibly functionalized with hydroxyl groups, R and R' are preferably C₁-C₃, most preferably methyl, R'' is preferably 2-hydroxyethyl or 2 hydroxypropyl, G is a saccharide, preferably glucose, and g is of from 1.5 to 8. All these surfactants are well known in the art. A more complete disclosure of glucose amides can be found for instance in WO 92-06154 and a more complete disclosure of alkyl polysaccharides can be found for instance in US 4,536,319. The compositions according to the present invention may comprise any of the above surfactants alone, or any combination thereof, depending on the end use envisioned. In the compositions herein, preferred long chain surfactants are selected from long chain alkyl sulfonates and long chain alkyl ethoxylates, and mixtures thereof.
  • The compositions according to the present invention further comprise at least one short chain surfactant, or mixtures thereof. The definition of short chain surfactants is as above for long chain surfactants, except that said alkyl group as said hydrophobic portion is a C₆ to C₁₀ alkyl group, and where said short chain surfactant is an alkyl ether carboxylate, said alkyl chain in said hydrophobic portion is a C₆-C₈ alkyl chain. Accordingly, suitable short chain surfactants for use herein include those listed herein above in the description of long chain surfactants, but with shorter alkyl chain.
  • Preferred short chain nonionic surfactants for use herein are alkyl alkoxylates according to the formula C₆-C₁₀(OCH₂CH₂)e(OCH₂CH₂CH₂)pOH, where e and p representing respectively the degree of ethoxylation and propoxylation are independently of from 0 to 20, and that e+p>0
    Figure imgb0002
    . Most preferred short chain nonionic surfactants for use herein are those where e and p are such that e+p is from 3 to 10, particularly those where p is 0 and e is from 3 to 8. Also, most preferred short chain nonionic surfactants for use herein are those where said short chain is a hydrocarbon chain comprising from 7 to 10 carbon atoms.
  • Said preferred short chain nonionic surfactants for use herein can be manufactured by the processes well known to the man skilled in the art, such as condensation of the corresponding alcohol and alkylene oxide, but such short chain surfactants are more conveniently commercially available for instance from Sidobre under the trade name Mergital@C4 (C8EO4), from Kolb under the trade names Imbentin@ AG/810/050 and AG/810/080 (respectively C8-10EO5 and C8-10EO8).
  • Preferred short chain anionic surfactants for use herein are C₆-C₁₀ alkyl sulfates (C₆-C₁₀SO4) and alkyl sulfonates (C₆-C₁₀SO₃). Most preferred are the C6-C8 alkyl sulfates and sulfonates. Such short chain anionic surfactants can be made by well known sulphation or sulphonation processes followed by neutralization, but said anionic short chain surfactants are more conveniently commercially available, for instance from Rhone Poulenc under the trade name Rhodapon@ OLS, or from Witco under the trade name Witconate@.
  • The compositions according to the present invention may comprise from 0.1 % to 50 % by weight of the total composition, preferably from 1% to 40%, most preferably from 1.5% to 30% of said short chain surfactants. The short chain surfactants herein act not only as active cleaning ingredients, but also as stabilizers. If short chain anionic surfactants are used, it is preferred to observe a minimum weight ratio of short chain anionic surfactant to longer chain surfactant of 1:10. If short chain nonionic surfactants are used, it is preferred to observe a minimum weight ratio of short chain nonionic to longer chain surfactant of 1:5.
  • Depending on the end use envisioned, the compositions herein may further comprise a variety of other optional ingredients including builders, alkanolamines, pH adjusting agents, perfumes in amounts of less than 15% by weight of the total composition, dyes, bleaches, enzymes and the like.
  • In some instances, it may be appropriate to include a suds suppressing system in the compositions herein. Said suds suppressing system can advantageously be a mixture of 2-alkyl alkanols as described for instance in DE 40 21 265, or mixtures thereof, with a C₈ to C₂₂ fatty acid, or mixtures thereof. Such a system is particularly advantageous as both ingredients appear to act in synergy. Thus even a very low amount of said system is enough to control suds efficiently. Accordingly, said system is present in amounts of from 0.1% to 5% by weight of the total composition, preferably 0.5% to 3%.
  • The compositions herein do not require the presence of a stabilizing compound. By stabilizing compound, it is meant herein a compound whose sole function is to enhance the physical stability of the composition. Such compounds are typically xylene or toluene sulphonate salts, and glycol ethers, including ethylene glycol monobutyl ether, diethylene glycol monobutyl ether, dipropylene glycol monobutyl ether, dipropylene glycol methyl ether, propylene glycol methyl ether, tripropylene glycol methyl ether, propylene glycol monobutyl ether and other various solvents suvh as ethanol and butanol. Accordingly, the compositions of the present invention are preferably substantially free of such stabilizing compounds.
  • The present invention further encompasses a method of cleaning a hard surface which comprises the steps of diluting a composition according to the preceding claims in water, then applying it to said hard surface. Depending on the exact formulation, the compositions herein may be used both neat and diluted from 10 to 500 times.
  • Examples
  • The present invention will be further illustrated by the following examples.
    I II III IV
    C₁₂/₁₅ alkyl ethoxylate EO₃ 3 3 - -
    C₁₃/₁₅ alkyl ethoxylate EO₇ - - 20 -
    C₁₃/₁₅ alkyl ethoxylate EO₃₀ 5 5 - -
    C₁₂/₁₄ alkyl sulfonate - - - 30
    C₈ alkyl sulfate - 10 10 10
    C₈ alkyl ethoxylate EO₆ - 9 - -
    Citric acid 3 3 1 -
    Monoethanolamine 3 3 1 -
    Triethanolamine - - 3 -
    Water & minors ----------up to 100%-------
  • All compositions were evaluated for their physical stability at 4°C, at room temperature (20°C), and at 50°C. Composition I, which is not within the invention, was a gel at 4°C, and an emulsion at room temperature and at 50°C. All other compositions, within the invention, were clear transparent liquids in the same conditions.
  • Other compositions were made by mixing the listed ingredients in the listed proportions.
    V VI VII VIII
    C₁₃/₁₅ alkyl ethoxylate EO₃ 4 3 5 1
    C₁₃/₁₅ alkyl ethoxylate EO₇ - - - 5
    c₇/₉ alkyl sulfate 7.5 - - -
    C₈ alkyl sulfate - 8 - 10
    C₈ alkyl sulfonate - - 10 -
    C₇/₉ alkyl ethoxylate EO₆ - - 10 5
    C₈/₁₀ alkyl ethoxylate EO₅ 10 9 - 9
    C₁₃/₁₅ alkyl ethoxylate EO₃₀ 6 4 3 5
    Na Paraffin Sulfonate - 5 - -
    Citric acid 3 - - 3
    2-hexyl decanol 1 0.6 1 -
    Palm Kernel Fatty Acid 0.4 0.4 1 -
    Sodium Carbonate - 3 - -
    Water & minors ----------up to 100%-------

Claims (10)

  1. A stable and clear concentrated cleaning composition comprising from 10 % to 80 % by weight of the total composition of water, less than 15 % perfume and at least one long chain surfactant comprising a C₁₁-C₂₄ alkyl chain as its hydrophobic portion, or mixtures thereof, characterized in that said composition further comprises at least one co-surfactant consisting of a short chain surfactant comprising a C₆-C₁₀ alkyl chain as its hydrophobic portion, or mixtures thereof, except where said short chain surfactant is an alkyl ether carboxylate, said alkyl chain as said hydrophobic portion is a C₆-C₈ alkyl chain.
  2. A composition according to claim 1 wherein said short chain surfactant or mixtures thereof represents from 0.1 % to 50 % by weight of the total composition, preferably from 1 % to 40%, most preferably from 1.5% to 30%.
  3. A composition according to the preceding claims wherein said short chain surfactant, or mixtures thereof is :
    - a nonionic surfactant according to the formula C₆-C₁₀(OCH₂CH₂)e(OCH₂CH₂CH₂)pOH, where e and p representing respectively the degree of ethoxylation and propoxylation are independently of from 0 to 20, and that e+p>0
    Figure imgb0003
    ; or
    - an anionic surfactant according to the formula C₆-C₁₀SO4 or C₆-C₁₀SO₃; or
    - Mixtures thereof.
  4. A composition according to claim 3 wherein e and p are such that e+p is from 3 to 10, preferably p is 0 and e is from 3 to 8.
  5. A composition according to claim 3 wherein said anionic surfactant is C₆-C₁₀SO4 or C₆-C₁₀SO₃.
  6. A composition according to the preceding claims which comprises from 30% to 70% by weight of the total composition of water.
  7. A composition according to any of the preceding claims wherein said long chain surfactants are selected from long chain alkyl sulfonates and long chain alkyl ethoxylates, and mixtures thereof.
  8. A composition according to any of the preceding claims which is substantially free of stabilizing compounds.
  9. A composition according to any of the preceding claims which comprises from 0.1% to 5% by weight of the total composition, preferably 0.5% to 3% of a suds suppressing system, said suds suppressing system comprising a 2-alkyl alkanol, or mixtures thereof and a C₈-C₂₂ fatty acid, or mixtures thereof.
  10. A method of cleaning a hard surface which comprises the steps of diluting a composition according to the preceding claims in water, then applying it to said hard surface.
EP93870125A 1993-03-19 1993-07-07 Concentrated cleaning compositions Withdrawn EP0616026A1 (en)

Priority Applications (12)

Application Number Priority Date Filing Date Title
EP93870125A EP0616026A1 (en) 1993-03-19 1993-07-07 Concentrated cleaning compositions
BR9406013A BR9406013A (en) 1993-03-19 1994-03-14 Concentrated cleaning compositions
NZ263393A NZ263393A (en) 1993-03-19 1994-03-14 Cleaning composition; stable, clear, concentrated composition comprising at least one long chain surfactant and stabilised by the additional presence of short chain surfactants
AU64073/94A AU6407394A (en) 1993-03-19 1994-03-14 Concentrated cleaning compositions
CA 2158542 CA2158542A1 (en) 1993-03-19 1994-03-14 Concentrated cleaning compositions
CN 94192052 CN1122611A (en) 1993-03-19 1994-03-14 Concentrated cleaning compositions
JP6521160A JPH08508765A (en) 1993-03-19 1994-03-14 Concentrated cleaning composition
PCT/US1994/002747 WO1994021767A1 (en) 1993-03-19 1994-03-14 Concentrated cleaning compositions
MA23446A MA23138A1 (en) 1993-03-19 1994-03-17 CONCENTRATED CLEANING COMPOSITIONS COMPRISING AT LEAST ONE SHORT ACHENED SURFACTANT
MA23445A MA23137A1 (en) 1993-03-19 1994-03-17 CONCENTRATED CLEANING COMPOSITION
NO953644A NO953644D0 (en) 1993-03-19 1995-09-15 Concentrated cleaning mixtures
FI954396A FI954396A (en) 1993-03-19 1995-09-18 Concentrated cleaning compositions

Applications Claiming Priority (3)

Application Number Priority Date Filing Date Title
EP93870050 1993-03-19
EP93870050A EP0616028A1 (en) 1993-03-19 1993-03-19 Cleaning compositions with short chain nonionic surfactants
EP93870125A EP0616026A1 (en) 1993-03-19 1993-07-07 Concentrated cleaning compositions

Publications (1)

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EP0616026A1 true EP0616026A1 (en) 1994-09-21

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EP (1) EP0616026A1 (en)
JP (1) JPH08508765A (en)
CN (1) CN1122611A (en)
AU (1) AU6407394A (en)
BR (1) BR9406013A (en)
CA (1) CA2158542A1 (en)
FI (1) FI954396A (en)
MA (1) MA23137A1 (en)
NO (1) NO953644D0 (en)
NZ (1) NZ263393A (en)
WO (1) WO1994021767A1 (en)

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WO1995021233A1 (en) * 1994-02-03 1995-08-10 The Procter & Gamble Company Aqueous cleaning compositions containing a 2-alkyl alkanol, h2o2, an anionic and a low hlb nonionic
WO1996036313A1 (en) * 1995-05-17 1996-11-21 Unilever Plc Aqueous liquid cleansing composition containing fatty acid soaps
EP0908534A1 (en) * 1997-09-16 1999-04-14 CHURCH & DWIGHT COMPANY, INC. Aqueous composition for low-temperature metal-cleaning and method of use
DE19814829A1 (en) * 1998-04-02 1999-10-07 Merz & Co Gmbh & Co Composition for machine cleaning and disinfecting medical instruments
WO2000029528A2 (en) * 1998-11-12 2000-05-25 Colgate-Palmolive Company Microemulsion liquid cleaning composition containing a short chain amphiphile
WO2003091190A1 (en) * 2002-04-26 2003-11-06 Basf Aktiengesellschaft Alkoxylate mixtures and detergents containing the same
WO2005049775A1 (en) * 2003-11-14 2005-06-02 The Procter & Gamble Company Liquid detergent composition comprising a solubilizing nonionic surfactant
WO2006008094A1 (en) 2004-07-16 2006-01-26 Basf Aktiengesellschaft Method for accelerating the cross-linking process in paints
AU2003205637B2 (en) * 2002-01-21 2008-04-03 Basf Aktiengesellschaft Alkylglycol alkoxylates or alkyldiglycol alkoxylates, mixtures thereof with tensides and their use
US7371716B2 (en) 2002-04-26 2008-05-13 Basf Aktiengesellschaft C10-alkanolalkoxylate mixtures and the use thereof
US7419552B2 (en) 2002-04-26 2008-09-02 Basf Aktiengesellschaft C10-alkanol alkoxylates and the use thereof
US20100069509A1 (en) * 2006-12-14 2010-03-18 Basf Se Nonionic emulsifiers for emulsion concentrates for spontaneous emulsification
WO2010070088A1 (en) 2008-12-18 2010-06-24 Basf Se Surfactant mixture comprising branched short-chained and branched long-chained components
WO2011003904A1 (en) 2009-07-10 2011-01-13 Basf Se Surfactant mixture having short- and long-chained components

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ES2177948T3 (en) 1996-03-14 2002-12-16 Johnson & Johnson Consumer COMPOSITIONS OF CLEANSING AND MOISTURIZING TENSIOACTIVE.
DE60022811T2 (en) 1999-03-12 2006-07-13 Pfizer Products Inc., Groton Oral preparations for reducing the sensitivity of the tooth nerve and the dental bone containing potassium salts
PT2796553T (en) 2000-03-30 2019-09-27 Massachusetts Inst Technology Rna sequence-specific mediators of rna interference
WO2002044321A2 (en) 2000-12-01 2002-06-06 MAX-PLANCK-Gesellschaft zur Förderung der Wissenschaften e.V. Rna interference mediating small rna molecules

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* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
WO1995021233A1 (en) * 1994-02-03 1995-08-10 The Procter & Gamble Company Aqueous cleaning compositions containing a 2-alkyl alkanol, h2o2, an anionic and a low hlb nonionic
WO1996036313A1 (en) * 1995-05-17 1996-11-21 Unilever Plc Aqueous liquid cleansing composition containing fatty acid soaps
EP0908534A1 (en) * 1997-09-16 1999-04-14 CHURCH & DWIGHT COMPANY, INC. Aqueous composition for low-temperature metal-cleaning and method of use
US6124253A (en) * 1997-09-16 2000-09-26 Church & Dwight Co., Inc. Aqueous composition for low-temperature metal-cleaning and method of use
DE19814829A1 (en) * 1998-04-02 1999-10-07 Merz & Co Gmbh & Co Composition for machine cleaning and disinfecting medical instruments
DE19814829C2 (en) * 1998-04-02 2001-04-12 Merz & Co Gmbh & Co Water-based cleaners and disinfectants, their use and methods for automated simultaneous cleaning and disinfection of medical instruments, in particular endoscopes
WO2000029528A2 (en) * 1998-11-12 2000-05-25 Colgate-Palmolive Company Microemulsion liquid cleaning composition containing a short chain amphiphile
WO2000029528A3 (en) * 1998-11-12 2000-10-05 Colgate Palmolive Co Microemulsion liquid cleaning composition containing a short chain amphiphile
AU2003205637B2 (en) * 2002-01-21 2008-04-03 Basf Aktiengesellschaft Alkylglycol alkoxylates or alkyldiglycol alkoxylates, mixtures thereof with tensides and their use
AU2003205637B8 (en) * 2002-01-21 2008-04-17 Basf Aktiengesellschaft Alkylglycol alkoxylates or alkyldiglycol alkoxylates, mixtures thereof with tensides and their use
US7371716B2 (en) 2002-04-26 2008-05-13 Basf Aktiengesellschaft C10-alkanolalkoxylate mixtures and the use thereof
CN1312099C (en) * 2002-04-26 2007-04-25 巴斯福股份公司 Alkoxylate mixtures and detergents containing the same
US7335235B2 (en) 2002-04-26 2008-02-26 Basf Akiengesellschaft Alkoxylate mixtures and detergents containing the same
WO2003091190A1 (en) * 2002-04-26 2003-11-06 Basf Aktiengesellschaft Alkoxylate mixtures and detergents containing the same
US7419552B2 (en) 2002-04-26 2008-09-02 Basf Aktiengesellschaft C10-alkanol alkoxylates and the use thereof
WO2005049775A1 (en) * 2003-11-14 2005-06-02 The Procter & Gamble Company Liquid detergent composition comprising a solubilizing nonionic surfactant
WO2006008094A1 (en) 2004-07-16 2006-01-26 Basf Aktiengesellschaft Method for accelerating the cross-linking process in paints
US7608653B2 (en) 2004-07-16 2009-10-27 Basf Aktiengesellschaft Method for accelerating the cross-linking process in paints
US20100069509A1 (en) * 2006-12-14 2010-03-18 Basf Se Nonionic emulsifiers for emulsion concentrates for spontaneous emulsification
WO2010070088A1 (en) 2008-12-18 2010-06-24 Basf Se Surfactant mixture comprising branched short-chained and branched long-chained components
WO2011003904A1 (en) 2009-07-10 2011-01-13 Basf Se Surfactant mixture having short- and long-chained components

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WO1994021767A1 (en) 1994-09-29
CN1122611A (en) 1996-05-15
JPH08508765A (en) 1996-09-17
CA2158542A1 (en) 1994-09-29
NO953644L (en) 1995-09-15
FI954396A (en) 1995-09-18
AU6407394A (en) 1994-10-11
NZ263393A (en) 1997-10-24
MA23137A1 (en) 1994-10-01
NO953644D0 (en) 1995-09-15
BR9406013A (en) 1996-01-02

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