WO1994021767A1 - Concentrated cleaning compositions - Google Patents

Concentrated cleaning compositions Download PDF

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Publication number
WO1994021767A1
WO1994021767A1 PCT/US1994/002747 US9402747W WO9421767A1 WO 1994021767 A1 WO1994021767 A1 WO 1994021767A1 US 9402747 W US9402747 W US 9402747W WO 9421767 A1 WO9421767 A1 WO 9421767A1
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WO
WIPO (PCT)
Prior art keywords
alkyl
surfactant
chain
mixtures
composition according
Prior art date
Application number
PCT/US1994/002747
Other languages
French (fr)
Inventor
Marc François Théophile EVERS
Vincent Reniers
Peter Rosalia Joannes Geboes
Massimo Morini
Louise Gail Scott
Original Assignee
The Procter & Gamble Company
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 The Procter & Gamble Company filed Critical The Procter & Gamble Company
Priority to JP6521160A priority Critical patent/JPH08508765A/en
Priority to BR9406013A priority patent/BR9406013A/en
Priority to NZ263393A priority patent/NZ263393A/en
Priority to AU64073/94A priority patent/AU6407394A/en
Publication of WO1994021767A1 publication Critical patent/WO1994021767A1/en
Priority to NO953644A priority patent/NO953644D0/en
Priority to FI954396A priority patent/FI954396A/en

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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 Cg-C ⁇ o 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 c l l ⁇ c 24 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 Cg-C ⁇ o 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 C 6 -Cg 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 %.
  • the 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 Cin to C 2 4 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 C 11 -C 2 4 alkyl sulfates (C 11 -C 24 S ⁇ ) , alkyl ether sulfates (Cn-C 4 (OCH 2 CH )eS ⁇ 4) , alkyl sulfonates (C - C 24 S0 3 ), alkyl succinates (C 11 -C 24 OOCCH 2 CH COOZ) , alkyl carboxylates (Ci 1 -C 24 COOM) , alkyl ether carboxylates (C ⁇ - C 24 (OCH 2 CH ) e COOM) , alkyl sarcosinates (C 11 -C 24 CON(CH 3 )R) , alkyl sulfo succinates (C 11 -C 2 4 ⁇ CCH(S ⁇ 3M)CH COOZ) , amine oxides (C 11 -C 2 4RR'NO) , glucose amides (C 11 -C 2 4RR
  • H or any counterion such as those known in the art, including Na, K, Li, NH 4 , 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 c - C5 alkyl groups, possibly functionalized with hydroxyl groups, R and R' are preferably C 1 -C 3 , most preferably methyl, R 1 ' 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.
  • 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 Cg to C ⁇ Q alkyl group, and where said short chain surfactant is an alkyl ether carboxylate, said alkyl chain in said hydrophobic portion is a Cg-Cg 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 C 6 - c l ⁇ ( O H 2 H 2)e( OCH 2 CH 2 CH 2)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 (C8E04) , from Kolb under the trade names Imbentin e AG/810/050 and AG/810/080 (respectively C8-10EO5 and C8-10EO8) •
  • Preferred short chain anionic surfactants for use herein are Cg-C 10 alkyl sulfates (Cs-C 10 S04) and alkyl sulfonates (C 6 -C 10 SO 3 ). 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 C 8 to C 22 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. Examples
  • 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.
  • Palm Kernel Fatty Acid 0.4 0.4 1

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

CONCENTRATED CLEANING COMPOSITIONS
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 Cg-C^o 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 cll~ 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 Cg-C^o 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-Cg 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 Cin 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-C24Sθ ) , alkyl ether sulfates (Cn-C 4(OCH2CH )eSθ4) , alkyl sulfonates (C - C24S03), alkyl succinates (C11-C24OOCCH2CH COOZ) , alkyl carboxylates (Ci1-C24COOM) , alkyl ether carboxylates (C^- C24(OCH2CH )eCOOM) , alkyl sarcosinates (C11-C24CON(CH3)R) , alkyl sulfo succinates (C11-C24θθCCH(Sθ3M)CH COOZ) , amine oxides (C11-C24RR'NO) , glucose amides (C11-C24CONRl 'X) , alkyl pyrrolidones (C11-C2 (C4H6θN) , alkylpolysaccharides (C11-C24OGg) , alkyl alkoxylates (cil- C24(OCH2CH2)e(OCH2CH2CH2)pOH) and betaines (Cn- C24N+(CH3) CH COO-) . In the formulae in brackets, 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 c - C5 alkyl groups, possibly functionalized with hydroxyl groups, R and R' are preferably C1-C3, most preferably methyl, R1' 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 Cg to C^Q alkyl group, and where said short chain surfactant is an alkyl ether carboxylate, said alkyl chain in said hydrophobic portion is a Cg-Cg 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- c lθ(O H2 H2)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. 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 (C8E04) , from Kolb under the trade names Imbentine AG/810/050 and AG/810/080 (respectively C8-10EO5 and C8-10EO8) •
Preferred short chain anionic surfactants for use herein are Cg-C10 alkyl sulfates (Cs-C10S04) 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/l5 alkyl ethoxylate E03 3 3 - -
C13/15 alkyl ethoxylate E07 - - 20 c13/l5 alkyl ethoxylate EO30 5 5 c12/l4 alkyl sulfonate - - - 30
C8 alkyl sulfate - 10 10 10
C8 alkyl ethoxylate E06 - 9 - -
Citric acid 3 3 1 -
Monoethanolamine 3 3 1 -
Triethanola ine - - 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 E03 1
C13/15 alkyl ethoxylate E07 5
C7/9 alkyl sulfate 7.5
C8 alkyl sulfate 10
C8 alkyl sulfonate 10
C7/9 alkyl ethoxylate E06 10 c δ/l0 alkyl ethoxylate E05 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

What is claimed is:
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 ~ι ~~ 2 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 Cg-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 4Q%, 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 Cg- 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; or
-an anionic surfactant according to the formula Cg- CιoS0 or C6-Cιoso3' 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 c 6~c10 so3.
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.
PCT/US1994/002747 1993-03-19 1994-03-14 Concentrated cleaning compositions WO1994021767A1 (en)

Priority Applications (6)

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JP6521160A JPH08508765A (en) 1993-03-19 1994-03-14 Concentrated cleaning composition
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
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 (4)

Application Number Priority Date Filing Date Title
EP93870050.7 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
EP93870125.7 1993-07-07

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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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US8420391B2 (en) 2000-03-30 2013-04-16 University Of Massachusetts RNA sequence-specific mediators of RNA interference
US8552171B2 (en) 2000-03-30 2013-10-08 University Of Massachusetts RNA sequence-specific mediators of RNA interference
US8632997B2 (en) 2000-03-30 2014-01-21 University Of Massachusetts RNA sequence-specific mediators of RNA interference
US8742092B2 (en) 2000-03-30 2014-06-03 University Of Massachusetts RNA sequence-specific mediators of RNA interference
US10472625B2 (en) 2000-03-30 2019-11-12 MAX-PLANCK-Gesellschaft zur Förderung der Wissenschaften e.V. RNA sequence-specific mediators of RNA interference
US9193753B2 (en) 2000-03-30 2015-11-24 University Of Massachusetts RNA sequence-specific mediators of RNA interference
US8394628B2 (en) 2000-03-30 2013-03-12 University Of Massachusetts RNA sequence-specific mediators of RNA interference
US9012621B2 (en) 2000-03-30 2015-04-21 MAX-PLANCK-Gesellschaft zur Förderung der Wissenschaften e.V. RNA sequence-specific mediators of RNA interference
US8933044B2 (en) 2000-12-01 2015-01-13 MAX-PLANCK-Gesellschaft zur Förderung der Wissenschaften e.V. RNA interference mediating small RNA molecules
US8993745B2 (en) 2000-12-01 2015-03-31 MAX-PLANCK-Gesellschaft zur Förderung der Wissenschaften e.V. RNA interference mediating small RNA molecules
US8895721B2 (en) 2000-12-01 2014-11-25 MAX-PLANCK-Gesellschaft zur Förderung der Wissenschaften e.V. RNA interference mediating small RNA molecules
US8895718B2 (en) 2000-12-01 2014-11-25 MAX-PLANCK-Gesellschaft zur Förderung der Wissenschaften e.V. RNA interference mediating small RNA molecules
US8853384B2 (en) 2000-12-01 2014-10-07 MAX-PLANCK-Gesellschaft zur Förderung der Wissenschaften e.V. RNA interference mediating small RNA molecules
US8372968B2 (en) 2000-12-01 2013-02-12 MAX-PLANCK-Gesellschaft zur Förderung der Wissenschaften e.V. RNA interference mediating small RNA molecules
US10633656B2 (en) 2000-12-01 2020-04-28 Max-Planck-Gesellschaft Zur Forderung Der Wissenschaften E.V. RNA interference mediating small RNA molecules

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NZ263393A (en) 1997-10-24
EP0616026A1 (en) 1994-09-21
AU6407394A (en) 1994-10-11
NO953644L (en) 1995-09-15
MA23137A1 (en) 1994-10-01
FI954396A0 (en) 1995-09-18
CA2158542A1 (en) 1994-09-29
JPH08508765A (en) 1996-09-17
FI954396A (en) 1995-09-18
NO953644D0 (en) 1995-09-15
BR9406013A (en) 1996-01-02
CN1122611A (en) 1996-05-15

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