EP0805200B1 - Hard surface cleaning compositions - Google Patents

Hard surface cleaning compositions Download PDF

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Publication number
EP0805200B1
EP0805200B1 EP96870058A EP96870058A EP0805200B1 EP 0805200 B1 EP0805200 B1 EP 0805200B1 EP 96870058 A EP96870058 A EP 96870058A EP 96870058 A EP96870058 A EP 96870058A EP 0805200 B1 EP0805200 B1 EP 0805200B1
Authority
EP
European Patent Office
Prior art keywords
alcohol
formula
integer
composition
ethoxylated
Prior art date
Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
Expired - Lifetime
Application number
EP96870058A
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German (de)
French (fr)
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EP0805200A1 (en
Inventor
Marc François Theophile Evers
Roberta Margherita Romano
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
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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 to ES96870058T priority Critical patent/ES2201165T3/en
Application filed by Procter and Gamble Co filed Critical Procter and Gamble Co
Priority to EP96870058A priority patent/EP0805200B1/en
Priority to DE69629104T priority patent/DE69629104T2/en
Priority to AT96870058T priority patent/ATE245187T1/en
Priority to TR1998/02219T priority patent/TR199802219T2/en
Priority to PCT/US1997/007228 priority patent/WO1997042276A1/en
Priority to JP9540003A priority patent/JPH11508321A/en
Priority to CZ983513A priority patent/CZ351398A3/en
Priority to AU30565/97A priority patent/AU3056597A/en
Priority to CA002253477A priority patent/CA2253477A1/en
Priority to US09/180,108 priority patent/US6828290B1/en
Publication of EP0805200A1 publication Critical patent/EP0805200A1/en
Application granted granted Critical
Publication of EP0805200B1 publication Critical patent/EP0805200B1/en
Anticipated expiration legal-status Critical
Expired - Lifetime 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
    • C11D3/2003Alcohols; Phenols
    • C11D3/2006Monohydric alcohols
    • C11D3/201Monohydric alcohols linear
    • C11D3/2013Monohydric alcohols linear fatty or with at least 8 carbon atoms in the alkyl chain
    • 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
    • C11D1/83Mixtures 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
    • C11D1/02Anionic 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
    • C11D1/02Anionic compounds
    • C11D1/12Sulfonic acids or sulfuric acid esters; Salts thereof
    • C11D1/29Sulfates of polyoxyalkylene ethers
    • 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

  • compositions for the cleaning of hard surfaces which clean effectively in concentrated or diluted form, and which leave no or little streaks after the cleaning.
  • the invention encompasses a hard surface cleaning composition comprising
  • the invention encompasses the use of said hard surface cleaning composition for improved shine of hard surfaces which have been cleaned therewith.
  • the invention further encompasses processes of cleaning hard surfaces with the compositions, either dilute or neat.
  • various components are combined and used in a hard surface cleaning composition with a view to provide shine to the hard surfaces which are cleaned with the compositions.
  • hard surfaces typically refers to floors, walls, windows, kitchen and bathroom furniture, appliances and dishes.
  • Obtaining a good shine end result is essentially the sum of two factors, namely: a good spreading of the cleaning product on the surface, and no crystallisation while drying. If both are achieved, a streak-free end result is obtained.
  • the streaking phenomenon can thus be described as the apparition of visible residues from the cleaning composition, as the water from the composition or the rinse water evaporates. Molecular crystallinity and aggregation during evaporation cause streaking, thus give a bad shine end result.
  • the ability of a composition to provide "shine" to surfaces refers to the composition's ability to leave little or no eye-visible residues on the surfaces, after evaporation of the water.
  • the ability of various compositions to provide shine can be evaluated by the human eye, but it is also possible to evaluate the difference by means of a gloss-meter, such as a Sheen ® 155 gloss meter.
  • a suitable method to evaluate a composition's ability to leave no or little residues is to first measure the gloss of a given surface, then apply the cleaning composition on the surface, then leave the composition to dry, and finally measure again the gloss of the surface on which the composition has been applied. The smaller the difference, the better the shine.
  • component (a) the compositions herein comprise a hydrophilic nonionic surfactant, or mixtures thereof.
  • Suitable hydrophilic nonionic surfactants for use herein include alkoxylated alcohols, preferably ethoxylated alcohols.
  • Such surfactants can be represented by the formula CxEOyH, where C symbolises the hydrocarbon chain of the alcohol starting material, x represents the length of its hydrocarbon chain.
  • EO represents ethoxy groups and y represents the average degree of ethoxylation, i.e. the average number of moles of ethoxy groups per mole of alcohol.
  • Suitable hydrophilic nonionic surfactants for use herein include those where x is of from 9 to 18, preferably 9 to 14, and average y is of from 8 to 30, preferably 10 to 20
  • suitable hydrophilic nonionic surfactants are ethoxylated and propoxylated alcohols which can be represented by the formula CxPOyEOy', where x is as above, and (y+y') is as y above.
  • the compositions herein can comprise mixtures of such hydrophilic nonionics, and the compositions comprise from 0.5% to 8.0%, preferably from 1% to 4% by weight of the total composition of such hydrophilic nonionic surfactants, or mixtures thereof.
  • compositions herein comprise a hydrophobic nonionic surfactant (c), or mixtures thereof.
  • Suitable hydrophobic nonionic surfactants for use herein include alkoxylated alcohols, preferably ethoxylated alcohols.
  • Such surfactants can be represented by the formula CxEOyH, where C symbolises the hydrocarbon chain of the alcohol starting material, x represents the length of its hydrocarbon chain.
  • EO represents ethoxy groups and y represents the average degree of ethoxylation, i.e. the average number of moles of ethoxy groups per mole of alcohol.
  • the compositions herein should comprise an anionic surfactant which is sulfated anionic surfactant, as opposed to a sulfonated anionic surfactant.
  • Suitable sulfated anionic surfactants for use herein include alkyl sulfates and alkoxylated alkyl sulfates which can be made by sulfating an alcohol, or an alcohol alkoxylate, respectively.
  • Typical alkoxylating groups for such surfactants are ethoxy and propoxy groups, and suitable alkyl ethoxy sulfates for use herein can be represented by the formula CxEOyS where C symbolises the hydrocarbon chain of the alcohol starting material, x represents the length of its hydrocarbon chain.
  • EO represents ethoxy groups and y represents the average degree of ethoxylation, i.e. the average number of moles of ethoxy groups per mole of alcohol.
  • S stands for a sulfate group.
  • Suitable alkyl ethoxy sulfates anionic surfactants for use herein include those where x is from 10 to 14 and y is from 1 to 5.
  • suitable alkyl propoxy sulfates can be represented as CxPOyS, with identical ranges for x and y.
  • a particular sulfated anionic surfactant for use herein is a mixture of an ethoxylated alkyl sulfate and a propoxylated alkyl sulfate according to the formulas above.
  • the compositions herein comprise from 0.5% to 10%, preferably from 0.5% to 4% of said sulfated anionic surfactant, or mixtures thereof.
  • An optional but highly preferred component herein is a particular builder system which further improves the cleaning performance without negatively affecting the shine.
  • This fifth component comprises a carbonate or polyphosphate salt, and a polycarboxylate salt, and preferably the weight ratio of polycarboxylate to carbonate or polyphosphate is at least 1:0.05.
  • salt refers to both the acidic form of all the builders suitable for use herein, or any of their salts.
  • Suitable carbonate builders for use herein are according to the formula X 2 CO 3 or XHCO 3 where X is a suitable counterion, typically K + , Na + NH 4 + .
  • Such suitable and preferred polycarboxylates include citrate and compounds of the formula CH(A)(COOX)-CH(COOX)-O-CH(COOX)-CH(COOX)(B) wherein A is H or OH; B is H or -O-CH(COOX)-CH 2 (COOX); and X is H or a salt-forming cation.
  • a and B are both H, then the compound is oxydissuccinic acid and its water-soluble salts.
  • A is OH and B is H, then the compound is tartrate monosuccinic acid (TMS) and its water-soluble salts.
  • TDS tartrate disuccinic acid
  • Still other ether polycarboxylates suitable for use herein include copolymers of maleic anhydride with ethylene or vinyl methyl ether, 1, 3, 5-trihydroxy benzene-2, 4, 6-trisulfonic acid, and carboxymethyloxysuccinic acid.
  • ether hydroxypolycarboxylate builders include the ether hydroxypolycarboxylates represented by the structure : HO-[C(R)(COOM)-C(R)(COOM)-O] n -H wherein M is hydrogen or a cation wherein the resultant salt is water-soluble, preferably an alkali metal, ammonium or substituted ammonium cation, n is from about 2 to about 15 (preferably n is from about 2 to about 10, more preferably n averages from about 2 to about 4) and each R is the same or different and selected from hydrogen, C 1-4 alkyl or C 1-4 substituted alkyl (preferably R is hydrogen).
  • polycarboxylates are those also known as alkyliminoacetic builders such as methyl imino diacetic acid, alanine diacetic acid, methyl glycine diacetic acid, hydroxy propylene imino diacetic acid and other alkyl imino acetic acid builders. Most preferred of all polycarboxylate builders for use herein is citrate.
  • compositions herein comprise from 0.5% to 5% by weight of the total composition of the builder system, preferably from 0.5% to 3%.
  • components (a) to (d) should be present in certain specified ratios. Accordingly, components (a) and (b) should be present in a weight ratio of (a) to (b) of from 1:1 to 10:1, preferably 2:1 to 7:1. Components (c) and (b) should be present in a weight ratio of (c) to (b) of from 5:1 to 25:1, preferably 10:1 to 20:1. And components (d) and (c) should be present in a weight ratio of (d) to (c) of from 1:1 to 1:10, preferably 1:2 to 1:6. Where a component is composed of a mixture of ingredients, as opposed to a single ingredient, the weight ratios herein are calculated on the basis of the weight amount of the component, i.e. the added amounts of the individual ingredients forming the component.
  • compositions herein are combining three technology blocks which function on their own, but which find their preferred application when they are used together.
  • the first technology block is the combination of the selected hydrophilic nonionic surfactant with the selected alcohol, in the selected ratios. Indeed, these nonionic surfactants are particularly effective on particulate soils and on greasy soils, but they will cause streaking if they are used on their own.
  • the second technology block is the combination of the selected hydrophobic nonionic surfactant with the selected alcohol in the selected ratios, together with the selected sulfate anionic surfactants.
  • these nonionic surfactants and anionic surfactants are particularly effective on particulate soils and on greasy soils, but they will cause streaking if they are used on their own. Addition of alcohol, in the selected ratios, results in a clear shine benefit.
  • the third technology block is the mixed builder system.
  • Polycarboxylates with surfactants would cause streaking, and carbonate or polyphosphates with surfactants would cause a crystalline film to be deposited on the surface.
  • the combination of these builders, together with surfactants leaves no visible streaks and no film. This performance improvement is particularly visible in presence of anionic surfactants, as these surfactants tend to form streaks already when pure.
  • compositions herein can further comprise a variety of further, optional, ingredients.
  • optionals include bleaches, enzymes, dyes, perfumes and other aesthetics.
  • compositions herein are preferably formulated as aqueous liquids. They can comprise from 1% to 30% by weight of the total composition of actives, i.e. from 99% to 70% water.
  • “neat” refers to a composition comprising that amount of actives.
  • the composition herein is applied neat onto a surface so as to clean the surface, and is optionally but preferably subsequently removed by rinsing with water.
  • the compositions is first diluted in water, typically from 40 to 320 times, and it is then applied to the surface to be cleaned. Thereafter, in this second mode, the composition can but does not necessarily have to be rinsed off of the surface.
  • the first mode is generally more convenient for heavily soiled surfaces while the second mode is generally more convenient for large and lightly soiled surfaces such as floors.

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  • 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)
  • Health & Medical Sciences (AREA)
  • Emergency Medicine (AREA)
  • Detergent Compositions (AREA)

Abstract

The cleaning of hard surfaces is addresses, where no visible streaks or residues are left on the surfaces which have been cleaned. The invention encompasses several embodiments which combine a hydrophilic nonionic surfactant with a selected alcohol, in specific ratios, or a hydrophobic nonionic surfactant with a selected alcohols and a sulfated anionic surfactant, in specific ratios, or all these components together.

Description

    Technical Field
  • The invention relates to the cleaning of hard surfaces, particularly but not exclusively floors.
  • Background
  • Compositions for the cleaning of hard surfaces have been extensively discussed in the art. It is desirable that such compositions should have, in addition to the ability to clean effectively, the ability to provide a good shine to the surfaces they have cleaned. However, surface shine is often compromised by residues of the compositions which are left on the surfaces, and which appear as streaks as water evaporation is completed.
  • This problem becomes more acute when the compositions are used without rinsing after cleaning, and when the compositions are formulated as concentrated compositions, which comprise more actives and less water.
  • It is thus an object of the present invention to provide compositions for the cleaning of hard surfaces, which clean effectively in concentrated or diluted form, and which leave no or little streaks after the cleaning.
  • Summary of the invention
  • In a first embodiment, the invention encompasses a hard surface cleaning composition comprising
  • (a)-a hydrophilic nonionic surfactant; and
  • (b)-a C8-C18 alcohol; and
  • (c)-a hydrophobic nonionic surfactant; and
  • (d)-a sulfated anionic surfactant;
  • in weight ratios of (a):(b) of from 1:1 to 10:1, of (c):(b) of from 5:1 to 25:1, and of (d):(c) of from 1:1 to 1:10, wherein:
    • said composition comprises from 0.5% to 8.0% by weight of said hydrophilic nonionic surfactant (a), or mixtures thereof, and wherein said hydrophilic nonionic surfactant is an ethoxylated alcohol of formula CxEOyH, or an ethoxylated and propoxylated alcohol of formula CxPOyEOy', wherein x is an integer of from 9 to 14, and y and (y+y') are an integer of from 8 to 30, wherein said composition comprises from 0.1% to 3% by weight of the total composition of said C8-C18 alcohol (6); wherein
    • said composition comprises from 1% to 20% by weight of said hydrophobic nonionic surfactant (c), or mixtures thereof, and wherein said hydrophobic nonionic surfactant is an ethoxylated alcohol of formula CxEOyH or an ethoxylated and propoxylated alcohol of formula CxPOyEOy', wherein x is an integer of from 9 to 16 and y and (y+y') is an integer of from 2 to 7; and wherein said composition comprises from 0.5% to 10% of said sulfated anionic surfactant.
  • In a second embodiment, the invention encompasses the use of said hard surface cleaning composition for improved shine of hard surfaces which have been cleaned therewith.
  • The invention further encompasses processes of cleaning hard surfaces with the compositions, either dilute or neat.
  • Detailed Description of the Invention The Hard Surfaces:
  • In some embodiments of the invention, various components are combined and used in a hard surface cleaning composition with a view to provide shine to the hard surfaces which are cleaned with the compositions. As used herein, "hard surfaces", typically refers to floors, walls, windows, kitchen and bathroom furniture, appliances and dishes.
  • Shine:
  • Obtaining a good shine end result is essentially the sum of two factors, namely: a good spreading of the cleaning product on the surface, and no crystallisation while drying. If both are achieved, a streak-free end result is obtained. The streaking phenomenon can thus be described as the apparition of visible residues from the cleaning composition, as the water from the composition or the rinse water evaporates. Molecular crystallinity and aggregation during evaporation cause streaking, thus give a bad shine end result. Thus, as used herein, the ability of a composition to provide "shine" to surfaces refers to the composition's ability to leave little or no eye-visible residues on the surfaces, after evaporation of the water. In most cases, the ability of various compositions to provide shine can be evaluated by the human eye, but it is also possible to evaluate the difference by means of a gloss-meter, such as a Sheen ® 155 gloss meter. A suitable method to evaluate a composition's ability to leave no or little residues is to first measure the gloss of a given surface, then apply the cleaning composition on the surface, then leave the composition to dry, and finally measure again the gloss of the surface on which the composition has been applied. The smaller the difference, the better the shine.
  • The Components:
  • As a first component, component (a), the compositions herein comprise a hydrophilic nonionic surfactant, or mixtures thereof. Suitable hydrophilic nonionic surfactants for use herein include alkoxylated alcohols, preferably ethoxylated alcohols. Such surfactants can be represented by the formula CxEOyH, where C symbolises the hydrocarbon chain of the alcohol starting material, x represents the length of its hydrocarbon chain. EO represents ethoxy groups and y represents the average degree of ethoxylation, i.e. the average number of moles of ethoxy groups per mole of alcohol. Suitable hydrophilic nonionic surfactants for use herein include those where x is of from 9 to 18, preferably 9 to 14, and average y is of from 8 to 30, preferably 10 to 20 Also suitable hydrophilic nonionic surfactants are ethoxylated and propoxylated alcohols which can be represented by the formula CxPOyEOy', where x is as above, and (y+y') is as y above. The compositions herein can comprise mixtures of such hydrophilic nonionics, and the compositions comprise from 0.5% to 8.0%, preferably from 1% to 4% by weight of the total composition of such hydrophilic nonionic surfactants, or mixtures thereof.
  • As a second component, component (b), the compositions herein comprise an alcohol having a hydrocarbon chain comprising 8 to 18 carbon atoms, preferably 12 to 16. The hydrocarbon chain can be branched or linear, and can be mono, di or polyalcohols. The compositions herein comprise from 0.1% to 3% by weight of the total composition of such alcohol, or mixtures thereof, preferably from 0.1% to 1%.
  • As a third component, the compositions herein comprise a hydrophobic nonionic surfactant (c), or mixtures thereof. Suitable hydrophobic nonionic surfactants for use herein include alkoxylated alcohols, preferably ethoxylated alcohols. Such surfactants can be represented by the formula CxEOyH, where C symbolises the hydrocarbon chain of the alcohol starting material, x represents the length of its hydrocarbon chain. EO represents ethoxy groups and y represents the average degree of ethoxylation, i.e. the average number of moles of ethoxy groups per mole of alcohol. Suitable hydrophobic nonionic surfactants for use herein include those where x is of from 9 to 18, preferably 9 to 16, and y is of from 2 to 7, preferably 4 to 7. Suitable hydrophobic nonionic surfactants also include ethoxylated and propoxylated alcohols which can be represented by the formula CxPOyEOy', where x is as above x and where (y+y') is as y above. The compositions herein can comprise mixtures of such hydrophobic nonionics, and the compositions comprise from 1% to 20%, preferably from 3% to 15% by weight of the total composition of such hydrophobic nonionic surfactants, or mixtures thereof.
  • As a fourth component, (d), the compositions herein should comprise an anionic surfactant which is sulfated anionic surfactant, as opposed to a sulfonated anionic surfactant. Suitable sulfated anionic surfactants for use herein include alkyl sulfates and alkoxylated alkyl sulfates which can be made by sulfating an alcohol, or an alcohol alkoxylate, respectively. Typical alkoxylating groups for such surfactants are ethoxy and propoxy groups, and suitable alkyl ethoxy sulfates for use herein can be represented by the formula CxEOyS where C symbolises the hydrocarbon chain of the alcohol starting material, x represents the length of its hydrocarbon chain. EO represents ethoxy groups and y represents the average degree of ethoxylation, i.e. the average number of moles of ethoxy groups per mole of alcohol. And S stands for a sulfate group. Suitable alkyl ethoxy sulfates anionic surfactants for use herein include those where x is from 10 to 14 and y is from 1 to 5. Identically, suitable alkyl propoxy sulfates can be represented as CxPOyS, with identical ranges for x and y.
  • A particular sulfated anionic surfactant for use herein is a mixture of an ethoxylated alkyl sulfate and a propoxylated alkyl sulfate according to the formulas above. The compositions herein comprise from 0.5% to 10%, preferably from 0.5% to 4% of said sulfated anionic surfactant, or mixtures thereof.
  • An optional but highly preferred component herein is a particular builder system which further improves the cleaning performance without negatively affecting the shine. This fifth component, comprises a carbonate or polyphosphate salt, and a polycarboxylate salt, and preferably the weight ratio of polycarboxylate to carbonate or polyphosphate is at least 1:0.05. As used herein, "salt" refers to both the acidic form of all the builders suitable for use herein, or any of their salts.
  • Suitable carbonate builders for use herein are according to the formula X2CO3 or XHCO3 where X is a suitable counterion, typically K+, Na+ NH4 +. Suitable polyphosphates for use herein include compounds of formula XaHbPO4, where a and b are integers such that a+b=3, and a or b can be 0, or XaHbP3O10 where a and b are such that a+b=5, and a or b can be 0, and where X is a suitable counterion, particularly K+, Na+ or NH4+.
  • Suitable polycarboxylates for use herein include organic polycarboxylates where the highest LogKa, measured at 25°C/0.1M ionic strength is between 3 and 8, wherein the sum of the LogKCa + LogKMg, measured at 25°C/0.1M ionic strength is higher than 4, and wherein LogKCa = LogKMg ± 2 units, preferably 1.5 units, measured at 25°C/0.1M ionic strength.
  • Such suitable and preferred polycarboxylates include citrate and compounds of the formula CH(A)(COOX)-CH(COOX)-O-CH(COOX)-CH(COOX)(B) wherein A is H or OH; B is H or -O-CH(COOX)-CH2(COOX); and X is H or a salt-forming cation. For example, if in the above general formula A and B are both H, then the compound is oxydissuccinic acid and its water-soluble salts. If A is OH and B is H, then the compound is tartrate monosuccinic acid (TMS) and its water-soluble salts. If A is H and B is -O-CH(COOX)-CH2(COOX), then the compound is tartrate disuccinic acid (TDS) and its water-soluble salts. Mixtures of these builders are especially preferred for use herein. Particularly TMS to TDS, these builders are disclosed in U.S. Patent 4,663,071, issued to Bush et al., on May 5, 1987.
  • Still other ether polycarboxylates suitable for use herein include copolymers of maleic anhydride with ethylene or vinyl methyl ether, 1, 3, 5-trihydroxy benzene-2, 4, 6-trisulfonic acid, and carboxymethyloxysuccinic acid.
  • Other useful polycarboxylate builders include the ether hydroxypolycarboxylates represented by the structure : HO-[C(R)(COOM)-C(R)(COOM)-O]n-H wherein M is hydrogen or a cation wherein the resultant salt is water-soluble, preferably an alkali metal, ammonium or substituted ammonium cation, n is from about 2 to about 15 (preferably n is from about 2 to about 10, more preferably n averages from about 2 to about 4) and each R is the same or different and selected from hydrogen, C1-4 alkyl or C1-4 substituted alkyl (preferably R is hydrogen).
  • Suitable ether polycarboxylates also include cyclic compounds, particularly alicyclic compounds, such as those described in U.S. Patents 3,923,679; 3,835,163; 4,158,635; 4,120,874 and 4,102,903, all of which are incorporated herein by reference.
  • Preferred amongst those cyclic compounds are dipicolinic acid and chelidanic acid.
  • Also suitable polycarboxylates for use herein are mellitic acid, succinic acid, polymaleic acid, benzene 1,3,5-tricarboxylic acid, benzene pentacarboxylic acid, and carboxymethyloxysuccinic acid, and soluble salts thereof.
  • Still suitable carboxylate builders herein include the carboxylated carbohydrates disclosed in U.S. Patent 3,723,322, Diehl, issued March 28, 1973, incorporated herein by reference.
  • Other suitable carboxylates for use herein, which do not meet the above criteria are alkali metal, ammonium and substituted ammonium salts of polyacetic acids. Examples of polyacetic acid builder salts are sodium, potassium, lithium, ammonium and substituted ammonium salts of ethylenediamine, tetraacetic acid and nitrilotriacetic acid.
  • Other suitable polycarboxylates are those also known as alkyliminoacetic builders such as methyl imino diacetic acid, alanine diacetic acid, methyl glycine diacetic acid, hydroxy propylene imino diacetic acid and other alkyl imino acetic acid builders.
    Most preferred of all polycarboxylate builders for use herein is citrate.
  • The compositions herein comprise from 0.5% to 5% by weight of the total composition of the builder system, preferably from 0.5% to 3%.
  • Another feature of the compositions herein is that components (a) to (d) should be present in certain specified ratios. Accordingly, components (a) and (b) should be present in a weight ratio of (a) to (b) of from 1:1 to 10:1, preferably 2:1 to 7:1. Components (c) and (b) should be present in a weight ratio of (c) to (b) of from 5:1 to 25:1, preferably 10:1 to 20:1. And components (d) and (c) should be present in a weight ratio of (d) to (c) of from 1:1 to 1:10, preferably 1:2 to 1:6. Where a component is composed of a mixture of ingredients, as opposed to a single ingredient, the weight ratios herein are calculated on the basis of the weight amount of the component, i.e. the added amounts of the individual ingredients forming the component.
  • It is speculated that the compositions herein are combining three technology blocks which function on their own, but which find their preferred application when they are used together.
  • The first technology block is the combination of the selected hydrophilic nonionic surfactant with the selected alcohol, in the selected ratios. Indeed, these nonionic surfactants are particularly effective on particulate soils and on greasy soils, but they will cause streaking if they are used on their own.
  • The second technology block is the combination of the selected hydrophobic nonionic surfactant with the selected alcohol in the selected ratios, together with the selected sulfate anionic surfactants. Similarly to the first building block, these nonionic surfactants and anionic surfactants are particularly effective on particulate soils and on greasy soils, but they will cause streaking if they are used on their own. Addition of alcohol, in the selected ratios, results in a clear shine benefit.
  • The third technology block is the mixed builder system. Polycarboxylates with surfactants would cause streaking, and carbonate or polyphosphates with surfactants would cause a crystalline film to be deposited on the surface. But the combination of these builders, together with surfactants, leaves no visible streaks and no film. This performance improvement is particularly visible in presence of anionic surfactants, as these surfactants tend to form streaks already when pure.
  • The compositions herein can further comprise a variety of further, optional, ingredients. Such optionals include bleaches, enzymes, dyes, perfumes and other aesthetics.
  • The compositions herein are preferably formulated as aqueous liquids. They can comprise from 1% to 30% by weight of the total composition of actives, i.e. from 99% to 70% water. As used herein, "neat" refers to a composition comprising that amount of actives.
  • In a first mode, the composition herein is applied neat onto a surface so as to clean the surface, and is optionally but preferably subsequently removed by rinsing with water. In a second mode, the compositions is first diluted in water, typically from 40 to 320 times, and it is then applied to the surface to be cleaned. Thereafter, in this second mode, the composition can but does not necessarily have to be rinsed off of the surface. The first mode is generally more convenient for heavily soiled surfaces while the second mode is generally more convenient for large and lightly soiled surfaces such as floors.
  • The invention is further illustrated by the following examples
    Figure 00100001
    Figure 00110001

Claims (10)

  1. A hard surface cleaning composition comprising
    (a)-a hydrophilic nonionic surfactant; and
    (b)-a C8-C18 alcohol; and
    (c)-a hydrophobic nonionic surfactant; and
    (d)-a sulfated anionic surfactant;
    in weight ratios of (a):(b) of from 1:1 to 10:1, of (c):(b) of from 5:1 to 25:1, and of (d):(c) of from 1:1 to 1:10, wherein:
    said composition comprises from 0.5% to 8.0% by weight of said. hydrophilic nonionic surfactant (a), or mixtures thereof, and wherein said hydrophilic nonionic surfactant is an ethoxylated alcohol of formula CxEOyH, or an ethoxylated and propoxylated alcohol of formula CxPOyEOy', wherein x is an integer of from 9 to 14, and y and (y+y') are an integer of from 8 to 30, wherein said composition comprises from 0.1% to 3% by weight of the total composition of said C8-C18 alochol (6); wherein
    said composition comprises from 1% to 20% by weight of said hydrophobic nonionic surfactant (c), or mixtures thereof, and wherein said hydrophobic nonionic surfactant is an ethoxylated alcohol of formula CxEOyH or an ethoxylated and propoxylated alcohol of formula CxPOyEOy', wherein x is an integer of from 9 to 16 and y and (y+y') is an integer of from 4 to 7; and wherein said composition comprises from 0.5% to 10% of said sulfated anionic surfactant.
  2. A composition according to claim 1, wherein said composition additionally comprises from 0.5% to 5% by weight of the total composition, preferably from 0.5% to 3%, of a builder system comprising a carbonate or a polyphosphate salt. and a polycarboxylate salt, preferably a citrate salt
  3. A composition or use according to claim 2, wherein the weight ratio of said carbonate or polyphosphate to said polycarboxylate is at least 1:0.05.
  4. A composition according to any of the preceding claims, wherein said hydrophilic nonionic surfactant is an ethoxylated alcohol of formula CxEOyH, or an ethoxylated and propoxylated alcohol of formula CxPOyEOy', wherein x is an integer of from 9 to 14, and y and (y+y') are an integer of 10 to 20.
  5. A composition according to any of the preceding claims, wherein said hydrophobic nonionic surfactant is an ethoxylated alcohol of formula CxEOyH or an ethoxylated and propoxylated alcohol of formula CxPOyEOy', wherein x is an integer of from 9 to 16 and y and (y+y') is an integer of from 4 to 6.
  6. A composition according to any of the preceding claim, wherein said alcohol (b) is a C12-C16 alcohol.
  7. A composition according to any of the preceding claims wherein said sulfated anionic surfactant (d) is a mixture of an ethoxylated alkyl sulfate of formula CxEOyS and a propoxylated alkyl sulfate of formula CxPOyS wherein x is an integer of from 10 to 14 and y is an integer of from 1 to 5.
  8. A process of cleaning a hard surface wherein a composition according to any of the claims 1 to 7 is applied neat onto the surface, and optionally subsequently rinsed off of the surface
  9. A process of cleaning a hard surface wherein a composition according to any of the claims 1 to 7 is diluted in water, then applied onto the surface, and subsequently optionally rinsed off of the surface.
  10. The use of a hard surface cleaning composition according to any of the claims 1 to 7 for improved shine of hard surfaces which have been cleaned therewith.
EP96870058A 1996-05-03 1996-05-03 Hard surface cleaning compositions Expired - Lifetime EP0805200B1 (en)

Priority Applications (11)

Application Number Priority Date Filing Date Title
EP96870058A EP0805200B1 (en) 1996-05-03 1996-05-03 Hard surface cleaning compositions
DE69629104T DE69629104T2 (en) 1996-05-03 1996-05-03 Hard surface cleaning compositions
AT96870058T ATE245187T1 (en) 1996-05-03 1996-05-03 CLEANING COMPOSITIONS FOR HARD SURFACES
ES96870058T ES2201165T3 (en) 1996-05-03 1996-05-03 CLEANING COMPOSITIONS OF HARD SURFACES.
PCT/US1997/007228 WO1997042276A1 (en) 1996-05-03 1997-05-01 Hard surface cleaning compositions
JP9540003A JPH11508321A (en) 1996-05-03 1997-05-01 Hard surface cleaning composition
TR1998/02219T TR199802219T2 (en) 1996-05-03 1997-05-01 Hard surface cleaning compounds.
CZ983513A CZ351398A3 (en) 1996-05-03 1997-05-01 Mixture for cleansing solid surfaces
AU30565/97A AU3056597A (en) 1996-05-03 1997-05-01 Hard surface cleaning compositions
CA002253477A CA2253477A1 (en) 1996-05-03 1997-05-01 Hard surface cleaning compositions
US09/180,108 US6828290B1 (en) 1996-05-03 1997-05-01 Hard surface cleaning compositions

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
EP96870058A EP0805200B1 (en) 1996-05-03 1996-05-03 Hard surface cleaning compositions

Publications (2)

Publication Number Publication Date
EP0805200A1 EP0805200A1 (en) 1997-11-05
EP0805200B1 true EP0805200B1 (en) 2003-07-16

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EP96870058A Expired - Lifetime EP0805200B1 (en) 1996-05-03 1996-05-03 Hard surface cleaning compositions

Country Status (10)

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EP (1) EP0805200B1 (en)
JP (1) JPH11508321A (en)
AT (1) ATE245187T1 (en)
AU (1) AU3056597A (en)
CA (1) CA2253477A1 (en)
CZ (1) CZ351398A3 (en)
DE (1) DE69629104T2 (en)
ES (1) ES2201165T3 (en)
TR (1) TR199802219T2 (en)
WO (1) WO1997042276A1 (en)

Cited By (2)

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US8172953B2 (en) 2009-11-06 2012-05-08 Ecolab Usa Inc. Alkyl polyglucosides and a propoxylated-ethoxylated extended chain surfactant
WO2014039302A1 (en) 2012-09-04 2014-03-13 Lubrizol Advanced Materials, Inc. Polyurethane/polyacrylic hybrid dispersions for shine applications in home care

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EP0948892A1 (en) * 1998-04-08 1999-10-13 The Procter & Gamble Company Disinfecting compositions and processes for disinfecting surfaces
AU2006330669A1 (en) * 2005-12-20 2007-07-05 Novozymes Biologicals, Inc. Surfactants systems for surface cleaning
JP5235102B2 (en) * 2008-06-16 2013-07-10 花王株式会社 Aqueous hair cleanser
US8071520B2 (en) 2009-11-06 2011-12-06 Ecolab Usa Inc. Sulfonated alkyl polyglucoside use for enhanced food soil removal
US8389463B2 (en) 2009-11-09 2013-03-05 Ecolab Usa Inc. Enhanced dispensing of solid compositions
US8216994B2 (en) 2009-11-09 2012-07-10 Ecolab Usa Inc. Phosphate functionalized alkyl polyglucosides used for enhanced food soil removal
US20150252310A1 (en) 2014-03-07 2015-09-10 Ecolab Usa Inc. Alkyl amides for enhanced food soil removal and asphalt dissolution
JP7547028B2 (en) * 2016-03-04 2024-09-09 エス.シー. ジョンソン アンド サン、インコーポレイテッド Neutral floor cleaner composition

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GB9027416D0 (en) * 1990-12-18 1991-02-06 Unilever Plc Detergent composition
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US5393468A (en) * 1993-07-14 1995-02-28 Colgate Palmolive Company Hard surface cleaner
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EP0666308B1 (en) * 1994-02-03 2000-08-09 The Procter & Gamble Company Multi-purpose liquid cleaning compositions
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* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US8172953B2 (en) 2009-11-06 2012-05-08 Ecolab Usa Inc. Alkyl polyglucosides and a propoxylated-ethoxylated extended chain surfactant
WO2014039302A1 (en) 2012-09-04 2014-03-13 Lubrizol Advanced Materials, Inc. Polyurethane/polyacrylic hybrid dispersions for shine applications in home care

Also Published As

Publication number Publication date
EP0805200A1 (en) 1997-11-05
JPH11508321A (en) 1999-07-21
ES2201165T3 (en) 2004-03-16
CA2253477A1 (en) 1997-11-13
DE69629104D1 (en) 2003-08-21
WO1997042276A1 (en) 1997-11-13
CZ351398A3 (en) 1999-04-14
ATE245187T1 (en) 2003-08-15
DE69629104T2 (en) 2004-04-22
TR199802219T2 (en) 1999-02-22
AU3056597A (en) 1997-11-26

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