CA2345635A1 - Cleaning compositions - Google Patents
Cleaning compositions Download PDFInfo
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- CA2345635A1 CA2345635A1 CA002345635A CA2345635A CA2345635A1 CA 2345635 A1 CA2345635 A1 CA 2345635A1 CA 002345635 A CA002345635 A CA 002345635A CA 2345635 A CA2345635 A CA 2345635A CA 2345635 A1 CA2345635 A1 CA 2345635A1
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Classifications
-
- C—CHEMISTRY; METALLURGY
- C11—ANIMAL OR VEGETABLE OILS, FATS, FATTY SUBSTANCES OR WAXES; FATTY ACIDS THEREFROM; DETERGENTS; CANDLES
- C11D—DETERGENT COMPOSITIONS; USE OF SINGLE SUBSTANCES AS DETERGENTS; SOAP OR SOAP-MAKING; RESIN SOAPS; RECOVERY OF GLYCEROL
- C11D3/00—Other compounding ingredients of detergent compositions covered in group C11D1/00
- C11D3/395—Bleaching agents
- C11D3/3956—Liquid compositions
-
- C—CHEMISTRY; METALLURGY
- C11—ANIMAL OR VEGETABLE OILS, FATS, FATTY SUBSTANCES OR WAXES; FATTY ACIDS THEREFROM; DETERGENTS; CANDLES
- C11D—DETERGENT COMPOSITIONS; USE OF SINGLE SUBSTANCES AS DETERGENTS; SOAP OR SOAP-MAKING; RESIN SOAPS; RECOVERY OF GLYCEROL
- C11D3/00—Other compounding ingredients of detergent compositions covered in group C11D1/00
- C11D3/16—Organic compounds
- C11D3/37—Polymers
- C11D3/3746—Macromolecular compounds obtained by reactions only involving carbon-to-carbon unsaturated bonds
- C11D3/3757—(Co)polymerised carboxylic acids, -anhydrides, -esters in solid and liquid compositions
- C11D3/3765—(Co)polymerised carboxylic acids, -anhydrides, -esters in solid and liquid compositions in liquid compositions
-
- C—CHEMISTRY; METALLURGY
- C11—ANIMAL OR VEGETABLE OILS, FATS, FATTY SUBSTANCES OR WAXES; FATTY ACIDS THEREFROM; DETERGENTS; CANDLES
- C11D—DETERGENT COMPOSITIONS; USE OF SINGLE SUBSTANCES AS DETERGENTS; SOAP OR SOAP-MAKING; RESIN SOAPS; RECOVERY OF GLYCEROL
- C11D1/00—Detergent compositions based essentially on surface-active compounds; Use of these compounds as a detergent
- C11D1/02—Anionic compounds
- C11D1/12—Sulfonic acids or sulfuric acid esters; Salts thereof
- C11D1/14—Sulfonic acids or sulfuric acid esters; Salts thereof derived from aliphatic hydrocarbons or mono-alcohols
- C11D1/146—Sulfuric acid esters
-
- C—CHEMISTRY; METALLURGY
- C11—ANIMAL OR VEGETABLE OILS, FATS, FATTY SUBSTANCES OR WAXES; FATTY ACIDS THEREFROM; DETERGENTS; CANDLES
- C11D—DETERGENT COMPOSITIONS; USE OF SINGLE SUBSTANCES AS DETERGENTS; SOAP OR SOAP-MAKING; RESIN SOAPS; RECOVERY OF GLYCEROL
- C11D1/00—Detergent compositions based essentially on surface-active compounds; Use of these compounds as a detergent
- C11D1/66—Non-ionic compounds
- C11D1/72—Ethers of polyoxyalkylene glycols
- C11D1/721—End blocked ethers
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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)
- Detergent Compositions (AREA)
Abstract
According to the present invention there is provided a cleaning composition comprising a polymeric thickening system of at least two homo or copolymers.
Description
CLEANING COMPOSITIONS
Field of the invention E
The present invention relates to cleaning compositions, especially to thickened liquid cleaning compositions exhibiting effective cleaning performance and viscosity.
Background of the invention Efficient cleaning performance and viscosity of the cleaning compositions are two requirements which drive consumer acceptance of cleaning products. Effective cleaning of surfaces is important, especially on greasy and oily soils and/or where the composition is thereafter diluted. However viscosity is also a key factor in the preparation of such a cleaning composition. The viscosity of the cleaning composition must be high enough to enable the cleaning compositions to remain on the surface being cleansed for a sufficiently long period of time to ensure effective cleaning. Such a requirement is of particular utility in cleaning compositions intended to be applied "as is" to non-horizontal structural surfaces such as walls, windows and sanitary fittings such as sinks, baths, showers, wash basins and WCs. More particularly, viscosities of 10 cps to 4000 cps are suitable.
Field of the invention E
The present invention relates to cleaning compositions, especially to thickened liquid cleaning compositions exhibiting effective cleaning performance and viscosity.
Background of the invention Efficient cleaning performance and viscosity of the cleaning compositions are two requirements which drive consumer acceptance of cleaning products. Effective cleaning of surfaces is important, especially on greasy and oily soils and/or where the composition is thereafter diluted. However viscosity is also a key factor in the preparation of such a cleaning composition. The viscosity of the cleaning composition must be high enough to enable the cleaning compositions to remain on the surface being cleansed for a sufficiently long period of time to ensure effective cleaning. Such a requirement is of particular utility in cleaning compositions intended to be applied "as is" to non-horizontal structural surfaces such as walls, windows and sanitary fittings such as sinks, baths, showers, wash basins and WCs. More particularly, viscosities of 10 cps to 4000 cps are suitable.
It is therefore an object of the present invention to provide cleaning compositions having effective cleaning performance and viscosity.
Thickened cleaning compositions are known in the art. The most commonly used thickener is a polycarboxylate polymer of high molecular weight i.e. in the range of 500 000 to 4 500 000. Furthermore for best results it is preferred that the polycarboxylate polymer is cross-linked. EP 834 549 and EP 812 904 both describe cleaning compositions comprising such polymeric thickeners. However the Applicant has found disadvantages in the use of such a polymeric thickeners in that whilst the polymer provides adequate increase in viscosity, the yield stress of the composition is also increased. The effect of the increase in yield stress is that the composition can become too thick such that it does not spread easily on the surface and is therefore difficult to use and/or rinse. In addition it has been found that occasionally air bubbles may become trapped in the composition during manufacture which are difficult to remove and not consumer acceptable.
The Applicant has now found that the polymeric thickening system described herein provides thickening of the composition without the disadvantages of the previously used thickening systems as described above.
Summary of the invention According to the present invention there is provided a cleaning composition comprising a polymeric thickening system comprising a polycarboxylate homo or copolymer having molecular weight in the range of from 500 000 to 4 500 000 and a polycarboxylate homo or copolymer having a molecular weight of from 500 to 10 000.
In another aspect of the invention, there is provided a method for cleaning a hard surface by applying on said surface an effective amount of a composition of the present invention.
Thickened cleaning compositions are known in the art. The most commonly used thickener is a polycarboxylate polymer of high molecular weight i.e. in the range of 500 000 to 4 500 000. Furthermore for best results it is preferred that the polycarboxylate polymer is cross-linked. EP 834 549 and EP 812 904 both describe cleaning compositions comprising such polymeric thickeners. However the Applicant has found disadvantages in the use of such a polymeric thickeners in that whilst the polymer provides adequate increase in viscosity, the yield stress of the composition is also increased. The effect of the increase in yield stress is that the composition can become too thick such that it does not spread easily on the surface and is therefore difficult to use and/or rinse. In addition it has been found that occasionally air bubbles may become trapped in the composition during manufacture which are difficult to remove and not consumer acceptable.
The Applicant has now found that the polymeric thickening system described herein provides thickening of the composition without the disadvantages of the previously used thickening systems as described above.
Summary of the invention According to the present invention there is provided a cleaning composition comprising a polymeric thickening system comprising a polycarboxylate homo or copolymer having molecular weight in the range of from 500 000 to 4 500 000 and a polycarboxylate homo or copolymer having a molecular weight of from 500 to 10 000.
In another aspect of the invention, there is provided a method for cleaning a hard surface by applying on said surface an effective amount of a composition of the present invention.
Detailed description of the invention Pofymeric Thickening System The compositions of the present invention comprise a polymeric thickening system. The benefits of using the polymers described herein versus others described in the art for example cellulosic polymers such as guar gum or xanthum gum, are that they are more stable in the presence of bleach (especially hypochlorite bleach), provide better thickening efficiency and do not elevate the yield stress value to levels that might cause flow problems.
The polymeric thickening system of the present invention comprises at least two polycarboxylate polymers; a high molecular weight and a low polycarboxylate homo or copolymer. By high molecular weight it is meant a polycarboxylate homo or copolymer having a molecular weight in the range of from 500 000 to 4 500 000, more preferably from 1 000 000 to 4 000 000.
Most preferred high molecular weight polymers for use herein contain from 0.5%
to 4% by weight of a cross-linking agent, wherein the cross-linking agent tends to interconnect linear strands of the polymers to form the resulting cross-linked products. Suitable cross-linking agents include the polyalkenyl polyethers.
Preferred homo- polymers include the poiyacryiate polymers. Preferred copolymers comprise acrylic acid monomers in combination with other monomers for malefic acid, malefic anhydride, nethacylic acid, suucinic acid, vinyl ester and/or mixtures thereof. Preferred monomers of the homo or copolymeric species contain a carboxylic group. The molecular weight of the carboxylate group-containing monomers typically varies from 25 to 200, preferably from 50 to 150, more preferably from 75 to 125. Further, other monomers may be present in the monomeric mixture, if desired, such as ethylene and propylene, which act as diluents.
Preferred high molecular weight polycarboxylate polymers for use herein are the polyacrylate polymers. Especially preferred polymers are those of the poiyacrylate type including those sold under the trade names Carbopol~
The polymeric thickening system of the present invention comprises at least two polycarboxylate polymers; a high molecular weight and a low polycarboxylate homo or copolymer. By high molecular weight it is meant a polycarboxylate homo or copolymer having a molecular weight in the range of from 500 000 to 4 500 000, more preferably from 1 000 000 to 4 000 000.
Most preferred high molecular weight polymers for use herein contain from 0.5%
to 4% by weight of a cross-linking agent, wherein the cross-linking agent tends to interconnect linear strands of the polymers to form the resulting cross-linked products. Suitable cross-linking agents include the polyalkenyl polyethers.
Preferred homo- polymers include the poiyacryiate polymers. Preferred copolymers comprise acrylic acid monomers in combination with other monomers for malefic acid, malefic anhydride, nethacylic acid, suucinic acid, vinyl ester and/or mixtures thereof. Preferred monomers of the homo or copolymeric species contain a carboxylic group. The molecular weight of the carboxylate group-containing monomers typically varies from 25 to 200, preferably from 50 to 150, more preferably from 75 to 125. Further, other monomers may be present in the monomeric mixture, if desired, such as ethylene and propylene, which act as diluents.
Preferred high molecular weight polycarboxylate polymers for use herein are the polyacrylate polymers. Especially preferred polymers are those of the poiyacrylate type including those sold under the trade names Carbopol~
(especially Carbopol ~ETD 2691 available form Goodrich), Acrysol~ ICS-1, Polygel~, and Sokalan~. Preferred poiyacrylate copolymers are those containing acrylic acid and alkyl (C5-C10) acrylate as monomers, (commercially available under the tradename Carbopol~ 1623, Carbopol~ 695 from BF Goodrich). Most preferred are copolymers of acrylic acid and malefic anhydride, (commercially available under the tradename Polygel~ DB, Polygel~ DV, Polygel~ DA) and copolymers of acrylic acid and vinyl ester (commercially available under the tradename Polygel~ DR from 3V Sigma)..
Mixtures of any of the high molecular weight polycarboxylate polymers, herein before described, may also be used.
The second component of the polymeric thickening system is a low molecular weight polycarboxylate homo or copolymer. By low molecular weight it is meant a polycarboxylate polymer having a molecular weight of from 500 to 10 000, more preferably from 800 to 6000, most preferably from 1000 to 4000.
Preferred low molecular weight homo-polymers are not cross-linked and are most preferably polyacrylates. Most preferred copolymers comprise acrylic acid in combination with at least one other type of monomer. An especially preferred tow molecular weight polymer is Polygel~ W30 available from 3V sigma.
The ratio of high molecular weight to low molecular weight polymer is preferably from 50:1 to 1: 10, more preferably from 30:1 to 1:1, most preferably from 10:1 to 5:1.
The compositions of the present invention are shear thinning, meaning viscosity is lowered with increasing shear rates. Viscosity is measured using any currently available, suitable viscosity measuring equipment. Viscosity of the composition is preferably in the range of from 10 cps to 4000 cps, more preferably from 50 to 1000cps, most preferably from 100 to 550cps when measured using a Carrimed Rheometer at 25 °C and a shear rate of from 10 to 100 s ~'.
The polymeric thickening system is preferably present at a level of from 0.1 %
to 10%, more preferably from 0.5% to 5% and most preferably from 0.7 to 2%.
Surfactant A highly preferred, but optional component of the cleaning composition described herein is a surfactant. The surfactant may be selected from anionic, non-ionic, 5 cationic, amphoteric, zwiterionic surfactants or mixtures thereof.
In a preferred aspect of the present invention, the cleaning composition comprises an anionic surfactant system as described in more detail in the Applicants copending patent application. The anionic surfactant system consists of at least one linear short-chain and one branched long chain anionic surfactant.
The anionic surfactants are selected from sulphates, suiphonates, alkoxylated sulphates (preferably propoxylated, more preferably ethoxylated), phosphates or mixtures thereof. The short chain surfactants has from 5 to 9 carbon atom whereas the long chain surfactant has from 10 to 16 carbon atoms.
A preferred short-chain surfactant is C7-9 Empimin available from Albright and Wilson. A preferred long-chain surfactant is C12-13 branched sulphate based on Isalchem 123 available from Albright and Wilson.
fn another preferred aspect, the surfactant system additionally comprises a branched short-chain anionic surfactant. A suitable such anionic surfactant is ethyl hexyl sulphate avaialble from Albright and Wilson under the tradename Empico10585/A.
Optional components The compositions according to the present invention may comprise a number of optional ingredients such as bleaching agents, fatty acids, radical scavengers, antimicrobial compounds, builders, chelants, buffers, bactericides, solvents, enzymes, hydrotropes, colorants, bleach activators, soil suspenders, dye transfer agents, brighteners, anti dusting agents, dispersants, dye transfer inhibitors, pigments, perfumes and dyes:
A highly preferred optional ingredient according to the present invention is a hypochlorite bleaching agent, preferably an alkali metal hypochlorite.
Advantageously, the compositions of the invention are stable in the presence of this bleaching agent. Although alkali metal hypochlorites are preferred other hypochlorite compounds may also be used herein and can be selected from calcium and magnesium hypochlorite. A preferred alkali metal hypochlorite for use herein is sodium hypochlorite. Compositions according to the present invention may comprise hypochlorite bleaching agents such that the content of active chlorine in the compositions is from 0.1 % to 4%, preferably from 0.5%
to 2% by weight.
Another optional component of the present invention is an alkali metal salt of a Cg-C1g fatty acid. Said fatty acids are used as suds suppressors. Suitable fatt~~
acids for use herein can be any Cg-C1 g fatty acid, preferably fully saturated, preferably a sodium, potassium or lithium salt, more preferably the sodium salt.
Suitable fatty acids may be selected from caprylic acid, capric acid, lauric acid, myristic acid, palmitic acid, stearic acid and mixtures of fatty acids suitably hardened, derived from natural sources such as tallow, coconut oil, ground oil and babassu oil. Other suitable suds suppressors include C10-18 alkoxylated capped alcohols. Most preferably however the suds suppressor consists of a mixture of fatty acid, preferably coconut fatty acid (e.g. Prifac 5900 available from Unichem) and alkoxylated capped alcohol, preferably C12-14 ethoxy butoxy methyl ether (e.g. Plurafac LF231 available from BASF). Compositions according to the present invention comprise from 0.1~% to 2%, preferably less than 0.6% by weight of the composition of fatty acids.
A further optional component of the present invention is a radical scavenger.
Said radical scavengers are used as stabilisers. A suitable radical scavenger for use herein is the aromatic molecule containing a carboxylic group ring substitution. Suitable examples of radical scavengers for use herein include the meta and para-chlorobenzoic acid, benzoic acid, meta- ortho- and para-methoxybenzoic acid, meta nitrobenzoic acid, para bromobenzoic acid, salicylic acid, 5-sulphosalicylic acid, 3,5-dimethyl salicylic acid and paratoluic acid.
Of the above materials, ortho-methoxybenzoic acid is preferred. Compositions according to the present invention comprise from 0.01 % to 1.5% by weight, preferably from 0.1 % to 0.8% by weight and more preferably from 0.2% to 0.5%
by weight of the composition of radical scavengers.
An optional requirement of the compositions according to the present invention is that the pH is greater than 10, preferably greater than 11, more preferably greater than 12. This is achieved by the addition of from 0.4% to 2% of a caustic alkali. Suitable caustic alkalis for use herein include sodium and potassium 7 PCT/US99/2248?
hydroxide. Compositions according to the present invention comprising hypochlorite preferably have a pH greater than 12 for hypochlorite stability.
The compositions according to the present invention are preferably aqueous and preferably comprise from 80% to 95%, more preferably from 85% to 90% of water.
The compositions according to the present invention are prepared by methods well known in the art such as the methods described in GB 1 329 086 with the exception of the polymer being pre-dispersed in an acidic water solution of pH
and then neutralised up to pH 7 before starting adding the other components.
The compositions according to the present invention can then be prepared by mixing all of the ingredients in a non-metallic apparatus at room temperature or in warm water. If fatty acid is used, it is melted before being added to the mixture.
Preferably, the surfactant blend is first prepared by adding the short chain surfactant to the long chain surfactants. Other optionals such as perfume and the alkali metal hypochlorite are then added whilst stirring. Colourants, if present, are added after all the other ingredients have been mixed.
The compositions according to the present invention preferably have a viscosity of from 10 cps to 4000 cps, more preferably from 50 cps to 2000 cps, most preferably from 150 cps to 1000 cps measured with a Carrimed Rheometer at a temperature of 25°C and a shear rate of 15-100 s-1. Where the composition is in a sprayed form, the viscosity of said spraying compositions is preferably of from 15 cps to 40 cps.
The compositions of the present invention may be used for a variety of cleaning purposes such as cleaning hard surfaces whereby said compositions thickened nature results in longer adhesion to the surface than non-thickened compositions. By "hard surface" it is meant herein any surface like bathroom, sanitary fittings such as sinks, showers, wash basins and WCs, kitchen, sinks, cooker tops, table tops, refrigerators, walls, windows and the like.
Packaging form of the compositions WO 00/2054' PCT/US99/224~2 The compositions herein may be packaged in a variety of suitable detergent packaging known to those skilled in the art. The liquid compositions herein may desirably be packaged in manually operated spray dispensing containers, which are usually made of synthetic organic polymeric plastic materials.
Accordingly, the present invention also encompasses liquid cleaning compositions of the invention packaged in a spray dispenser, preferably in a trigger spray dispenser.
indeed, said spray-type dispensers allow to uniformly apply to a relatively large area of a surface to be cleaned the liquid cleaning compositions suitable for use according to the present invention; thereby contributing to the cleaning properties of said compositions. Such spray-type dispensers are particularly suitable to clean vertical surfaces. Surprisingly, the spraying of a liquid composition containing a polycarboxyiate polymer, contrary to compositions which do not contain the poiycarboxylate polymer, has been seen beneficial for preventing ors reducing inhalation of the composition by the user as said composition is_ sprayed.
The present advantage is preferably observed where the cleaning composition is as defined hereinbefore. Accordingly, the use of a poiycarboxyiate polymer in a liquid cleaning composition is provided, said composition being in a sprayed form, for preventing or reducing inhalation of said composition by the user as said composition is sprayed. Preferably, the liquid cleaning composition is as defined hereinbefore.
Suitable spray-type dispensers to be used according to the present invention include manually operated foam trigger-type dispensers sold for example by Specialty Packaging Products, Inc. or Continental Sprayers, Inc. These types of dispensers are disclosed, for instance, in US-4,701,311 to Dunnining et al.
and US-4,646,973 and US-4,538,745 both to Focarracci. Particularly preferred to be used herein ace spray-type dispensers such as T 8500~ or T 8900~
commercially available from Continental Spray International or T 8100~
commercially available from Canyon, Northern Ireland. In such a dispenser the liquid composition is divided in fine liquid droplets resulting in a spray that is directed onto the surface to be treated. Indeed, in such a spray-type dispenser the composition contained in the body of said dispenser is directed through the spray-type dispenser head via energy communicated to a pumping mechanism WO 00/20547 PCT/iJS99/22482 by the user as said user activates said pumping mechanism. More particularly, in said spray-type dispenser head the composition is forced against an obstacle, e.g. a grid or a cone or the like, thereby providing shocks to help atomise the liquid composition, i.e. to help the formation of liquid droplets.
The present invention further encompasses a method for cleaning a hard surface by applying on said surface an effective amount of a composition of the invention. The said composition may be applied in its neat form or after having been diluted with water. Preferably said composition is.diluted up to 200 times its weight of water, preferably into 50 to 150 times its weight of water and more preferably 75 to 95, before it is applied to said surface. When the composition is diluted prior to use (to reach a total active level in the order of 1.2%), the composition will still advantageously provide effective cleaning performance.
In the preferred embodiment of the method of the present invention wherein sail composition is applied to a hard-surface to be cleaned in its diluted form, it may_ not be necessary to rinse the surface after the composition has been applied.
WO 00/20547 PCT/US99/22a82 Examples The examples provided below are not intended to be limiting and merely provide an example of the sort of formulation that is envisaged by the Applicant. All amounts are listed in % weight of the total composition.
IA B C
w/w % w/w % w/w Hi h MW of mer #1 1.0 - 1.0 Low MW of mer 0.1 0.1 0.1 Hi h MW of mer #2 ~ - I 1.5 -Heptyl-nonyl sulfate 1.5 1.5 I 3.0 Em imin LN from A&W
Capped nonionic alcohol - - 0.1 Plurafac LF231 from BASF
Coconut fatty acid - - 0.1 Prifac 5900 from Unichema 2 ethyl-hexyl sulfate 1.5 1.5 -Em icol 0585/A from A8~W
C12-C13 branched sulfate1.0 1.0 1.0 based on Isalchem123 Citrus Bleach PCMF erfume0.3 0.3 0.2 H ochlorite 1.0 1.0 1.0 Caustic 1.0 1.0 1.0 Green d a 0.0058 0.0058 0.0058 Periodic acid 0.01 0.01 0.01 Sodium silicate 0.4 0.4 0.4 Demineralized water Balance Balance Balance High MW polymer #1 is Polygel DR from 3Vsigma High MW polymer #2 is Carbopol ETD2691 from Goodrich Low MW polymer is Polygel W30 from 3Vsigma
Mixtures of any of the high molecular weight polycarboxylate polymers, herein before described, may also be used.
The second component of the polymeric thickening system is a low molecular weight polycarboxylate homo or copolymer. By low molecular weight it is meant a polycarboxylate polymer having a molecular weight of from 500 to 10 000, more preferably from 800 to 6000, most preferably from 1000 to 4000.
Preferred low molecular weight homo-polymers are not cross-linked and are most preferably polyacrylates. Most preferred copolymers comprise acrylic acid in combination with at least one other type of monomer. An especially preferred tow molecular weight polymer is Polygel~ W30 available from 3V sigma.
The ratio of high molecular weight to low molecular weight polymer is preferably from 50:1 to 1: 10, more preferably from 30:1 to 1:1, most preferably from 10:1 to 5:1.
The compositions of the present invention are shear thinning, meaning viscosity is lowered with increasing shear rates. Viscosity is measured using any currently available, suitable viscosity measuring equipment. Viscosity of the composition is preferably in the range of from 10 cps to 4000 cps, more preferably from 50 to 1000cps, most preferably from 100 to 550cps when measured using a Carrimed Rheometer at 25 °C and a shear rate of from 10 to 100 s ~'.
The polymeric thickening system is preferably present at a level of from 0.1 %
to 10%, more preferably from 0.5% to 5% and most preferably from 0.7 to 2%.
Surfactant A highly preferred, but optional component of the cleaning composition described herein is a surfactant. The surfactant may be selected from anionic, non-ionic, 5 cationic, amphoteric, zwiterionic surfactants or mixtures thereof.
In a preferred aspect of the present invention, the cleaning composition comprises an anionic surfactant system as described in more detail in the Applicants copending patent application. The anionic surfactant system consists of at least one linear short-chain and one branched long chain anionic surfactant.
The anionic surfactants are selected from sulphates, suiphonates, alkoxylated sulphates (preferably propoxylated, more preferably ethoxylated), phosphates or mixtures thereof. The short chain surfactants has from 5 to 9 carbon atom whereas the long chain surfactant has from 10 to 16 carbon atoms.
A preferred short-chain surfactant is C7-9 Empimin available from Albright and Wilson. A preferred long-chain surfactant is C12-13 branched sulphate based on Isalchem 123 available from Albright and Wilson.
fn another preferred aspect, the surfactant system additionally comprises a branched short-chain anionic surfactant. A suitable such anionic surfactant is ethyl hexyl sulphate avaialble from Albright and Wilson under the tradename Empico10585/A.
Optional components The compositions according to the present invention may comprise a number of optional ingredients such as bleaching agents, fatty acids, radical scavengers, antimicrobial compounds, builders, chelants, buffers, bactericides, solvents, enzymes, hydrotropes, colorants, bleach activators, soil suspenders, dye transfer agents, brighteners, anti dusting agents, dispersants, dye transfer inhibitors, pigments, perfumes and dyes:
A highly preferred optional ingredient according to the present invention is a hypochlorite bleaching agent, preferably an alkali metal hypochlorite.
Advantageously, the compositions of the invention are stable in the presence of this bleaching agent. Although alkali metal hypochlorites are preferred other hypochlorite compounds may also be used herein and can be selected from calcium and magnesium hypochlorite. A preferred alkali metal hypochlorite for use herein is sodium hypochlorite. Compositions according to the present invention may comprise hypochlorite bleaching agents such that the content of active chlorine in the compositions is from 0.1 % to 4%, preferably from 0.5%
to 2% by weight.
Another optional component of the present invention is an alkali metal salt of a Cg-C1g fatty acid. Said fatty acids are used as suds suppressors. Suitable fatt~~
acids for use herein can be any Cg-C1 g fatty acid, preferably fully saturated, preferably a sodium, potassium or lithium salt, more preferably the sodium salt.
Suitable fatty acids may be selected from caprylic acid, capric acid, lauric acid, myristic acid, palmitic acid, stearic acid and mixtures of fatty acids suitably hardened, derived from natural sources such as tallow, coconut oil, ground oil and babassu oil. Other suitable suds suppressors include C10-18 alkoxylated capped alcohols. Most preferably however the suds suppressor consists of a mixture of fatty acid, preferably coconut fatty acid (e.g. Prifac 5900 available from Unichem) and alkoxylated capped alcohol, preferably C12-14 ethoxy butoxy methyl ether (e.g. Plurafac LF231 available from BASF). Compositions according to the present invention comprise from 0.1~% to 2%, preferably less than 0.6% by weight of the composition of fatty acids.
A further optional component of the present invention is a radical scavenger.
Said radical scavengers are used as stabilisers. A suitable radical scavenger for use herein is the aromatic molecule containing a carboxylic group ring substitution. Suitable examples of radical scavengers for use herein include the meta and para-chlorobenzoic acid, benzoic acid, meta- ortho- and para-methoxybenzoic acid, meta nitrobenzoic acid, para bromobenzoic acid, salicylic acid, 5-sulphosalicylic acid, 3,5-dimethyl salicylic acid and paratoluic acid.
Of the above materials, ortho-methoxybenzoic acid is preferred. Compositions according to the present invention comprise from 0.01 % to 1.5% by weight, preferably from 0.1 % to 0.8% by weight and more preferably from 0.2% to 0.5%
by weight of the composition of radical scavengers.
An optional requirement of the compositions according to the present invention is that the pH is greater than 10, preferably greater than 11, more preferably greater than 12. This is achieved by the addition of from 0.4% to 2% of a caustic alkali. Suitable caustic alkalis for use herein include sodium and potassium 7 PCT/US99/2248?
hydroxide. Compositions according to the present invention comprising hypochlorite preferably have a pH greater than 12 for hypochlorite stability.
The compositions according to the present invention are preferably aqueous and preferably comprise from 80% to 95%, more preferably from 85% to 90% of water.
The compositions according to the present invention are prepared by methods well known in the art such as the methods described in GB 1 329 086 with the exception of the polymer being pre-dispersed in an acidic water solution of pH
and then neutralised up to pH 7 before starting adding the other components.
The compositions according to the present invention can then be prepared by mixing all of the ingredients in a non-metallic apparatus at room temperature or in warm water. If fatty acid is used, it is melted before being added to the mixture.
Preferably, the surfactant blend is first prepared by adding the short chain surfactant to the long chain surfactants. Other optionals such as perfume and the alkali metal hypochlorite are then added whilst stirring. Colourants, if present, are added after all the other ingredients have been mixed.
The compositions according to the present invention preferably have a viscosity of from 10 cps to 4000 cps, more preferably from 50 cps to 2000 cps, most preferably from 150 cps to 1000 cps measured with a Carrimed Rheometer at a temperature of 25°C and a shear rate of 15-100 s-1. Where the composition is in a sprayed form, the viscosity of said spraying compositions is preferably of from 15 cps to 40 cps.
The compositions of the present invention may be used for a variety of cleaning purposes such as cleaning hard surfaces whereby said compositions thickened nature results in longer adhesion to the surface than non-thickened compositions. By "hard surface" it is meant herein any surface like bathroom, sanitary fittings such as sinks, showers, wash basins and WCs, kitchen, sinks, cooker tops, table tops, refrigerators, walls, windows and the like.
Packaging form of the compositions WO 00/2054' PCT/US99/224~2 The compositions herein may be packaged in a variety of suitable detergent packaging known to those skilled in the art. The liquid compositions herein may desirably be packaged in manually operated spray dispensing containers, which are usually made of synthetic organic polymeric plastic materials.
Accordingly, the present invention also encompasses liquid cleaning compositions of the invention packaged in a spray dispenser, preferably in a trigger spray dispenser.
indeed, said spray-type dispensers allow to uniformly apply to a relatively large area of a surface to be cleaned the liquid cleaning compositions suitable for use according to the present invention; thereby contributing to the cleaning properties of said compositions. Such spray-type dispensers are particularly suitable to clean vertical surfaces. Surprisingly, the spraying of a liquid composition containing a polycarboxyiate polymer, contrary to compositions which do not contain the poiycarboxylate polymer, has been seen beneficial for preventing ors reducing inhalation of the composition by the user as said composition is_ sprayed.
The present advantage is preferably observed where the cleaning composition is as defined hereinbefore. Accordingly, the use of a poiycarboxyiate polymer in a liquid cleaning composition is provided, said composition being in a sprayed form, for preventing or reducing inhalation of said composition by the user as said composition is sprayed. Preferably, the liquid cleaning composition is as defined hereinbefore.
Suitable spray-type dispensers to be used according to the present invention include manually operated foam trigger-type dispensers sold for example by Specialty Packaging Products, Inc. or Continental Sprayers, Inc. These types of dispensers are disclosed, for instance, in US-4,701,311 to Dunnining et al.
and US-4,646,973 and US-4,538,745 both to Focarracci. Particularly preferred to be used herein ace spray-type dispensers such as T 8500~ or T 8900~
commercially available from Continental Spray International or T 8100~
commercially available from Canyon, Northern Ireland. In such a dispenser the liquid composition is divided in fine liquid droplets resulting in a spray that is directed onto the surface to be treated. Indeed, in such a spray-type dispenser the composition contained in the body of said dispenser is directed through the spray-type dispenser head via energy communicated to a pumping mechanism WO 00/20547 PCT/iJS99/22482 by the user as said user activates said pumping mechanism. More particularly, in said spray-type dispenser head the composition is forced against an obstacle, e.g. a grid or a cone or the like, thereby providing shocks to help atomise the liquid composition, i.e. to help the formation of liquid droplets.
The present invention further encompasses a method for cleaning a hard surface by applying on said surface an effective amount of a composition of the invention. The said composition may be applied in its neat form or after having been diluted with water. Preferably said composition is.diluted up to 200 times its weight of water, preferably into 50 to 150 times its weight of water and more preferably 75 to 95, before it is applied to said surface. When the composition is diluted prior to use (to reach a total active level in the order of 1.2%), the composition will still advantageously provide effective cleaning performance.
In the preferred embodiment of the method of the present invention wherein sail composition is applied to a hard-surface to be cleaned in its diluted form, it may_ not be necessary to rinse the surface after the composition has been applied.
WO 00/20547 PCT/US99/22a82 Examples The examples provided below are not intended to be limiting and merely provide an example of the sort of formulation that is envisaged by the Applicant. All amounts are listed in % weight of the total composition.
IA B C
w/w % w/w % w/w Hi h MW of mer #1 1.0 - 1.0 Low MW of mer 0.1 0.1 0.1 Hi h MW of mer #2 ~ - I 1.5 -Heptyl-nonyl sulfate 1.5 1.5 I 3.0 Em imin LN from A&W
Capped nonionic alcohol - - 0.1 Plurafac LF231 from BASF
Coconut fatty acid - - 0.1 Prifac 5900 from Unichema 2 ethyl-hexyl sulfate 1.5 1.5 -Em icol 0585/A from A8~W
C12-C13 branched sulfate1.0 1.0 1.0 based on Isalchem123 Citrus Bleach PCMF erfume0.3 0.3 0.2 H ochlorite 1.0 1.0 1.0 Caustic 1.0 1.0 1.0 Green d a 0.0058 0.0058 0.0058 Periodic acid 0.01 0.01 0.01 Sodium silicate 0.4 0.4 0.4 Demineralized water Balance Balance Balance High MW polymer #1 is Polygel DR from 3Vsigma High MW polymer #2 is Carbopol ETD2691 from Goodrich Low MW polymer is Polygel W30 from 3Vsigma
Claims (8)
1. A cleaning composition comprising a polymeric thickening system comprising a first polycarboxylate homo or copolymer having molecular weight in the range of from 500 000 to 4 500 000 and a second polycarboxylate homo or copolymer having molecular weight in the range of from 500 to 10 000.
2. A cleaning composition according to claim 1 wherein the first polycarboxylate polymer is a polyacrylate polymer
3. A cleaning composition according to any of the preceding claims wherein the first polymer is cross-linked.
4. A cleaning composition according to any of the preceding claims wherein the second polycarboxylate polymer is a polyacylate polymer which is not cross-linked.
5. A cleaning composition according to any of the preceding claims wherein both the first and second polymers are copolymers containing at least two monomer types, wherein at least one of the monomers is acrylic acid.
6. A cleaning composition according to any of the preceding claims wherein the ratio of the first to the second polymer is 50:1 to 1: 10.
7. A cleaning composition according to any of the preceding claims wherein the viscosity of the composition is in the range of from 10 cps to 4000 cps measured as described herein.
8. A method of cleaning a surface by applying a composition according to any of the preceding claims to the surface and optionally subsequently rinsing.
Applications Claiming Priority (3)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| EP98870208A EP0992574A1 (en) | 1998-10-05 | 1998-10-05 | Cleaning compositions |
| EP98870208.0 | 1998-10-05 | ||
| PCT/US1999/022482 WO2000020547A1 (en) | 1998-10-05 | 1999-09-28 | Cleaning compositions |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| CA2345635A1 true CA2345635A1 (en) | 2000-04-13 |
Family
ID=8237100
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| CA002345635A Abandoned CA2345635A1 (en) | 1998-10-05 | 1999-09-28 | Cleaning compositions |
Country Status (9)
| Country | Link |
|---|---|
| EP (1) | EP0992574A1 (en) |
| JP (1) | JP2002526641A (en) |
| AR (1) | AR013292A1 (en) |
| AU (1) | AU6271499A (en) |
| BR (1) | BR9914271A (en) |
| CA (1) | CA2345635A1 (en) |
| PE (1) | PE20001196A1 (en) |
| TR (1) | TR200100935T2 (en) |
| WO (1) | WO2000020547A1 (en) |
Families Citing this family (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| EP4276162A3 (en) * | 2015-11-13 | 2024-01-31 | The Procter & Gamble Company | Cleaning compositions containing branched alkyl sulfate surfactants and linear alkyl sulfate surfactants |
| JP2020169324A (en) * | 2020-06-04 | 2020-10-15 | ザ プロクター アンド ギャンブル カンパニーＴｈｅ Ｐｒｏｃｔｅｒ ＆ Ｇａｍｂｌｅ Ｃｏｍｐａｎｙ | Cleaning compositions containing branched alkyl sulfate surfactants and linear alkyl sulfate surfactants |
Family Cites Families (3)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| AU1617092A (en) * | 1991-06-07 | 1992-12-10 | Colgate-Palmolive Company, The | Linear viscoelastic aqueous liquid detergent composition, especially for automatic dishwashers of improved high temperature stability |
| EP0517313A1 (en) * | 1991-06-07 | 1992-12-09 | Colgate-Palmolive Company | Linear viscoelastic aqueous liquid detergent composition, especially for automatic dishwashers, of improved high temperature stability |
| JPH11501067A (en) * | 1995-02-28 | 1999-01-26 | ケイ ケミカル カンパニー | Concentrated liquid gel detergent for dishwashing |
-
1998
- 1998-10-05 EP EP98870208A patent/EP0992574A1/en not_active Withdrawn
-
1999
- 1999-09-28 CA CA002345635A patent/CA2345635A1/en not_active Abandoned
- 1999-09-28 WO PCT/US1999/022482 patent/WO2000020547A1/en active Application Filing
- 1999-09-28 TR TR2001/00935T patent/TR200100935T2/en unknown
- 1999-09-28 JP JP2000574646A patent/JP2002526641A/en not_active Withdrawn
- 1999-09-28 AU AU62714/99A patent/AU6271499A/en not_active Abandoned
- 1999-09-28 BR BR9914271-6A patent/BR9914271A/en not_active Application Discontinuation
- 1999-10-01 PE PE1999000999A patent/PE20001196A1/en not_active Application Discontinuation
- 1999-10-05 AR ARP990105043A patent/AR013292A1/en unknown
Also Published As
| Publication number | Publication date |
|---|---|
| JP2002526641A (en) | 2002-08-20 |
| BR9914271A (en) | 2001-07-03 |
| TR200100935T2 (en) | 2001-10-22 |
| PE20001196A1 (en) | 2000-11-10 |
| AU6271499A (en) | 2000-04-26 |
| EP0992574A1 (en) | 2000-04-12 |
| WO2000020547A1 (en) | 2000-04-13 |
| AR013292A1 (en) | 2000-12-13 |
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| EEER | Examination request | ||
| FZDE | Dead |