EP0813585B1 - Cleaning compositions - Google Patents

Cleaning compositions Download PDF

Info

Publication number
EP0813585B1
EP0813585B1 EP96944872A EP96944872A EP0813585B1 EP 0813585 B1 EP0813585 B1 EP 0813585B1 EP 96944872 A EP96944872 A EP 96944872A EP 96944872 A EP96944872 A EP 96944872A EP 0813585 B1 EP0813585 B1 EP 0813585B1
Authority
EP
European Patent Office
Prior art keywords
composition
amine oxide
acid
viscosity
weight
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
EP96944872A
Other languages
German (de)
French (fr)
Other versions
EP0813585A1 (en
Inventor
Balvinder Adat
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.)
SC Johnson and Son Inc
Original Assignee
SC Johnson and Son Inc
Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)
Filing date
Publication date
Application filed by SC Johnson and Son Inc filed Critical SC Johnson and Son Inc
Publication of EP0813585A1 publication Critical patent/EP0813585A1/en
Application granted granted Critical
Publication of EP0813585B1 publication Critical patent/EP0813585B1/en
Anticipated expiration legal-status Critical
Expired - Lifetime legal-status Critical Current

Links

Classifications

    • CCHEMISTRY; METALLURGY
    • C11ANIMAL OR VEGETABLE OILS, FATS, FATTY SUBSTANCES OR WAXES; FATTY ACIDS THEREFROM; DETERGENTS; CANDLES
    • C11DDETERGENT COMPOSITIONS; USE OF SINGLE SUBSTANCES AS DETERGENTS; SOAP OR SOAP-MAKING; RESIN SOAPS; RECOVERY OF GLYCEROL
    • C11D3/00Other compounding ingredients of detergent compositions covered in group C11D1/00
    • C11D3/02Inorganic compounds ; Elemental compounds
    • C11D3/04Water-soluble compounds
    • C11D3/042Acids
    • 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
    • C11D3/34Organic compounds containing sulfur
    • CCHEMISTRY; METALLURGY
    • C11ANIMAL OR VEGETABLE OILS, FATS, FATTY SUBSTANCES OR WAXES; FATTY ACIDS THEREFROM; DETERGENTS; CANDLES
    • C11DDETERGENT COMPOSITIONS; USE OF SINGLE SUBSTANCES AS DETERGENTS; SOAP OR SOAP-MAKING; RESIN SOAPS; RECOVERY OF GLYCEROL
    • C11D1/00Detergent compositions based essentially on surface-active compounds; Use of these compounds as a detergent
    • C11D1/66Non-ionic compounds
    • C11D1/75Amino oxides
    • 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
    • C11D17/00Detergent materials or soaps characterised by their shape or physical properties
    • 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
    • C11D17/00Detergent materials or soaps characterised by their shape or physical properties
    • C11D17/0008Detergent materials or soaps characterised by their shape or physical properties aqueous liquid non soap compositions
    • C11D17/003Colloidal solutions, e.g. gels; Thixotropic solutions or pastes
    • 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
    • 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
    • C11D3/2086Hydroxy carboxylic acids-salts thereof

Definitions

  • This invention relates to foamable cleaning compositions for use in removing limescale stains from surfaces.
  • Tap water always contains a certain amount of solubilized ions which eventually deposit as salts, on surfaces in contact with the water, as it evaporates.
  • salts include calcium carbonate, commonly referred to as limescale.
  • limescale This phenomenon of limescale accumulation on surfaces which are often in contact with water may damage surfaces and affects the functioning of taps or appliances, such as irons.
  • the accumulation of limescale in the toilet bowl is aesthetically unpleasant and favors the deposition of further soil and the growth of microorganisms. It is therefore important to control this limescale accumulation.
  • EP-A-0,589,761 discloses a thickened acidic aqueous cleaner for bathtubs and other hard surfaced items, which removes limescale, soap scum and greasy soil from surfaces of such items without damaging such surfaces.
  • composition of the reference comprises:
  • EP-A-0,606,712 discloses a thickened buffered aqueous acidic composition.
  • composition of the reference comprises citric acid and sodium citrate, and in the composition suitable thickeners include conventional thickeners such as xanthan gum, polymers, alkyl amines, and surfactant based thickeners as well as nonionic and amine oxide surfactants.
  • suitable thickeners include conventional thickeners such as xanthan gum, polymers, alkyl amines, and surfactant based thickeners as well as nonionic and amine oxide surfactants.
  • the composition of the reference does not include sulphamic acid.
  • EP-A-0,666,304 discloses compositions comprising as a first essential ingredient an organic acid such as maleic acid. It is preferred in the invention of the reference to use maleic acid either alone or together with sulfonic acids such as sulfamic acid.
  • compositions according to the reference invention comprises as a second essential ingredient a surfactant or mixtures thereof.
  • the compositions comprise said surfactant in an appropriate amount below 1% by weight of the total composition.
  • the composition of the reference does not include amine oxide surfactants.
  • the compositions of the reference comprise thickeners.
  • WO-A-94 28108 concerns over cleaning compositions and does not deal with acidic limescale removing compositions.
  • EP-A-0130786 discloses an acidic cleaning composition comprising water, a mixture of a weak inorganic acid and a weak organic acid, an amine oxide surfactant, and a surface-tension-reducing co-solvent.
  • the subject invention is directed to a limescale removing composition which can be delivered as a foam.
  • the subject invention provides an aqueous liquid storage-stable foamable limescale removing composition consisting of:
  • the subject invention provides a method of removing limescale from a substrate comprising the steps of:
  • the composition of the invention comprises a mixture of sulphamic acid and at least one organic carboxylic acid.
  • the sulphamic acid and the at least one other acid are preferably mixed in synergistically effective limescale removing amounts.
  • the organic carboxylic acid has a molecular weight of 60-250. More preferably, the carboxylic acid is lactic acid, citric acid, or another hydroxy acid where the hydroxy group is ⁇ to at least one of the acid moieties.
  • the mixture of acids is present in the range 5-20 weight percent of the aqueous cleaning composition and more preferably 10-20 weight percent.
  • the composition of the invention can be dispensed as a foam through a foam dispenser.
  • the composition may tend to be difficult to dispense in this way if the composition in use has a final viscosity which is much above 300 cps. All viscosity measurements stated herein are taken using a Brookfield viscometer, at 20°C using #3 spindle at 30 rpm. Preferably, the final viscosity is in the range 200-300 cps.
  • the maximum viscosity of the composition of the invention is limited by the need for the composition to be dispensable through a foam dispenser, one aspect of particular importance is storage stability.
  • the composition of the subject invention relies on a complex blend of components and inevitably the composition will be placed into its final package some long time before it comes into use in the hands of the ultimate consumer. It is important that the viscosity of the composition is maintained within parameters during storage to allow delivery through the foam dispenser. Long term stability of the viscosity is mainly determined by the optimized level and type of thickening agents. Thickeners which are effective in the composition of the subject invention are selected from the group consisting of acrylic emulsion polymer thickeners, xanthan gums, rhamsan gums, welan gums and polyurethanes. The preferred thickener is xanthan gum with altered rheology. The thickener is present in an amount of 0.001-5 weight percent based on the weight of the cleaning composition.
  • the storage stable composition of the subject invention will preferably be dispensable as a foam through a foam dispenser after storage at room temperature for 6 months, and more preferable after storage at room temperature for 1 year.
  • the storage stable composition of the subject invention will not show phase separation or precipitation after said storage, the viscosity of the composition remaining constant during said storage.
  • the foaminess index ⁇ is between 15-50 and more typically between 20-30.
  • the amount of thickener is instrumental in allowing the composition to remain storage stable, it should also be noted that the presence of particular amounts of other components in the composition may effect viscosity.
  • the amine oxide surfactant can be expected to have an effect on the viscosity of the composition.
  • composition is dispensable as a foam.
  • Dispensing as a foam allows the composition to remain on the limescale stain for an effective time.
  • the composition should be able to remain in contact with and be able to wet and penetrate the limescale stain for a sufficient time to have an effective descaling effect. Subsequently, the composition must be able to be washed away easily with water.
  • foams can be loose airy type foams, while at the other extreme, foams can be tight mousse like type foams.
  • the composition of the subject invention ideally produces a foam which is roughly halfway between a loose airy type foam and a tight mousse type foam in order to give maximum descaling and a good cling parameter.
  • Cling is measured by spraying about 10g of product onto the underside of a preweighed suspended plate weighing about 200g. The plate is left to hang for 5 minutes and is then re-weighed. The cling is determined by the amount of product remaining on the plate after 5 minutes.
  • the cling parameter of the composition of the subject invention is 50 - 70% of product remaining on the surface after 5 minutes.
  • the nature and amount of the amine oxide surfactant present in the composition of the invention will generally determine the foam profile and cling parameter of the composition. Additionally, however, the cling parameter is dependent on the amount of thickener present in the composition.
  • the amine oxide preferably has the formula RR' R"NO, where R is a substituted or unsubstituted alkyl or alkene group containing from 8 to 30, preferably from 10 to 20, more preferably 10 to 16 carbon atoms.
  • R is an unsubstituted alkyl group.
  • Groups R' and R" are each substituted or unsubstituted alkyl or alkene groups containing from 1 to 18, preferably from 1 to 4, carbon atoms. More preferably, R' and R" are each methyl groups.
  • the amine oxide detergent surfactant can be prepared by known and conventional methods.
  • One such method involves the oxidation of tertiary amines in the manner set forth in U.S. Patent No. 3,223,647 and British Patent 437,566.
  • amine oxides are prepared by the controlled oxidation of the corresponding tertiary amines.
  • the surfactant will be lauryl dimethyl amine oxide.
  • the amine oxide surfactant is present in the amount of 2.0-8.0% by weight of the total composition.
  • composition can contain other optional components appropriate to limescale removing compositions including dyes and fragrances.
  • composition of the invention (to 100 weight percent) is deionized water.
  • composition of the invention is dispensable through a conventional foam dispenser.
  • compositions of the invention are now set out below:
  • Example 3 had a viscosity of 250 cps and on dispensing through a conventional foam dispenser produced a foam with a cling parameter of 50 - 70% over a 5 minute period.
  • the composition was stable on storage at room temperature for one year.
  • Example 3 The composition of Example 3 was tested for effectiveness by the marble cube test as follows:
  • the average % weight loss (for the 3 cubes) ranged from 35 - 40%.
  • a commercially available maleic acid limescale removing composition was tested in the same way as above and the % weight loss ranged from 20 - 30%.
  • the subject invention provides a limescale removing composition which may be produced using conventional manufacturing methods and packaging.
  • the foamable limescale removing composition maintains its foaming and rheological properties after shelf storage at room temperature for 6 months, preferably one year. This shelf stability will allow a consumer to effectively utilize the descaling composition even though the composition may be placed into its final package a long time prior to its purchase and use.

Abstract

An aqueous liquid storage stable foamable limescale removing composition comprising a mixture of sulphamic acid and at least one organic carboxylic acid, a thickening agent and an amine oxide surfactant.

Description

    Technical Field
  • This invention relates to foamable cleaning compositions for use in removing limescale stains from surfaces.
  • Background Art
  • Tap water always contains a certain amount of solubilized ions which eventually deposit as salts, on surfaces in contact with the water, as it evaporates. Such salts include calcium carbonate, commonly referred to as limescale. This phenomenon of limescale accumulation on surfaces which are often in contact with water may damage surfaces and affects the functioning of taps or appliances, such as irons. Also, the accumulation of limescale in the toilet bowl is aesthetically unpleasant and favors the deposition of further soil and the growth of microorganisms. It is therefore important to control this limescale accumulation.
  • Many limescale removing compositions are known in the art. For example, EP-A-0,589,761 discloses a thickened acidic aqueous cleaner for bathtubs and other hard surfaced items, which removes limescale, soap scum and greasy soil from surfaces of such items without damaging such surfaces.
  • One composition of the reference comprises:
  • (a) an anionic surfactant;
  • (b) a nonionic surfactant;
  • (c) a xanthan gum thickener having a molecular weight of about 1,000,000 to 10,000,000 such as Kelzan® T sold by Merck & Co.; and
  • (d) 2 to 8 percent of an acid mixture of succinic acid; glutaric acid and adipic acid of about 1:1:1; and
  • (e) balance being water, wherein the composition has a pH of about 1 to about 4, more preferably about 2.7 to about 3.3 and a Brookfield viscosity of about 200 to 1,000 cps at room temperature using a #2 spindle and 50 rpm. The composition of the reference does not include either sulfamic acid or amine oxide surfactants.
  • EP-A-0,606,712 discloses a thickened buffered aqueous acidic composition.
  • The composition of the reference comprises citric acid and sodium citrate, and in the composition suitable thickeners include conventional thickeners such as xanthan gum, polymers, alkyl amines, and surfactant based thickeners as well as nonionic and amine oxide surfactants. The composition of the reference does not include sulphamic acid.
  • EP-A-0,666,304 discloses compositions comprising as a first essential ingredient an organic acid such as maleic acid. It is preferred in the invention of the reference to use maleic acid either alone or together with sulfonic acids such as sulfamic acid.
  • The compositions according to the reference invention comprises as a second essential ingredient a surfactant or mixtures thereof. The compositions comprise said surfactant in an appropriate amount below 1% by weight of the total composition. The composition of the reference does not include amine oxide surfactants. Optionally, the compositions of the reference comprise thickeners.
  • WO-A-94 28108 concerns over cleaning compositions and does not deal with acidic limescale removing compositions.
  • EP-A-0130786 discloses an acidic cleaning composition comprising water, a mixture of a weak inorganic acid and a weak organic acid, an amine oxide surfactant, and a surface-tension-reducing co-solvent.
  • The subject invention is directed to a limescale removing composition which can be delivered as a foam.
  • In one embodiment, the subject invention provides an aqueous liquid storage-stable foamable limescale removing composition consisting of:
  • a. from 5% to 20% by weight of a mixture of sulphamic acid and at least one organic carboxylic acid;
  • b. from 0.001% to 5% by weight of a thickening agent selected from acrylic emulsion polymer thickeners, xanthan gums, rhamsan gums, welan gums and polyurethane;
  • c. from 2% to 8% by weight of an amine oxide surfactant,
  • d. optionally a dye;
  • e. optionally a fragrance; and
  • f. deionized water to balance
  • wherein the viscosity of the composition is 300 cps or less, the viscosity being measured using a Brookfield viscometer at 20°C using #3 spindle at 30 rpm.
  • In another embodiment, the subject invention provides a method of removing limescale from a substrate comprising the steps of:
  • applying the composition of the present invention to a substrate containing limescale;
  • allowing the composition to remain in contact with the substrate for a sufficient amount of time to have a descaling effect; and
  • removing the composition from the substrate.
  • Disclosure of Invention
  • All amounts of components set out herein are given as percentages by weight of the limescale removing composition.
  • The composition of the invention comprises a mixture of sulphamic acid and at least one organic carboxylic acid. The sulphamic acid and the at least one other acid are preferably mixed in synergistically effective limescale removing amounts. Preferably, the organic carboxylic acid has a molecular weight of 60-250. More preferably, the carboxylic acid is lactic acid, citric acid, or another hydroxy acid where the hydroxy group is α to at least one of the acid moieties.
  • The mixture of acids is present in the range 5-20 weight percent of the aqueous cleaning composition and more preferably 10-20 weight percent.
  • The composition of the invention can be dispensed as a foam through a foam dispenser. The composition may tend to be difficult to dispense in this way if the composition in use has a final viscosity which is much above 300 cps. All viscosity measurements stated herein are taken using a Brookfield viscometer, at 20°C using #3 spindle at 30 rpm. Preferably, the final viscosity is in the range 200-300 cps. When the maximum viscosity of the composition of the invention is limited by the need for the composition to be dispensable through a foam dispenser, one aspect of particular importance is storage stability. The composition of the subject invention relies on a complex blend of components and inevitably the composition will be placed into its final package some long time before it comes into use in the hands of the ultimate consumer. It is important that the viscosity of the composition is maintained within parameters during storage to allow delivery through the foam dispenser. Long term stability of the viscosity is mainly determined by the optimized level and type of thickening agents. Thickeners which are effective in the composition of the subject invention are selected from the group consisting of acrylic emulsion polymer thickeners, xanthan gums, rhamsan gums, welan gums and polyurethanes. The preferred thickener is xanthan gum with altered rheology. The thickener is present in an amount of 0.001-5 weight percent based on the weight of the cleaning composition.
  • The storage stable composition of the subject invention will preferably be dispensable as a foam through a foam dispenser after storage at room temperature for 6 months, and more preferable after storage at room temperature for 1 year. Preferably, the storage stable composition of the subject invention will not show phase separation or precipitation after said storage, the viscosity of the composition remaining constant during said storage.
  • Typically, the foaminess index Σ is between 15-50 and more typically between 20-30.
  • While the amount of thickener is instrumental in allowing the composition to remain storage stable, it should also be noted that the presence of particular amounts of other components in the composition may effect viscosity. In particular, the amine oxide surfactant can be expected to have an effect on the viscosity of the composition.
  • Another important feature of the limescale removing composition of the invention is that the composition is dispensable as a foam.
  • Dispensing as a foam allows the composition to remain on the limescale stain for an effective time. The composition should be able to remain in contact with and be able to wet and penetrate the limescale stain for a sufficient time to have an effective descaling effect. Subsequently, the composition must be able to be washed away easily with water.
  • Of importance, therefore, in the effectiveness of the composition is the quality of the foam which is produced. At one extreme, foams can be loose airy type foams, while at the other extreme, foams can be tight mousse like type foams. The composition of the subject invention ideally produces a foam which is roughly halfway between a loose airy type foam and a tight mousse type foam in order to give maximum descaling and a good cling parameter. Cling is measured by spraying about 10g of product onto the underside of a preweighed suspended plate weighing about 200g. The plate is left to hang for 5 minutes and is then re-weighed. The cling is determined by the amount of product remaining on the plate after 5 minutes. Preferably, the cling parameter of the composition of the subject invention is 50 - 70% of product remaining on the surface after 5 minutes.
  • The nature and amount of the amine oxide surfactant present in the composition of the invention will generally determine the foam profile and cling parameter of the composition. Additionally, however, the cling parameter is dependent on the amount of thickener present in the composition. The amine oxide preferably has the formula RR' R"NO, where R is a substituted or unsubstituted alkyl or alkene group containing from 8 to 30, preferably from 10 to 20, more preferably 10 to 16 carbon atoms. Preferably, R is an unsubstituted alkyl group. Groups R' and R" are each substituted or unsubstituted alkyl or alkene groups containing from 1 to 18, preferably from 1 to 4, carbon atoms. More preferably, R' and R" are each methyl groups.
  • The amine oxide detergent surfactant can be prepared by known and conventional methods. One such method involves the oxidation of tertiary amines in the manner set forth in U.S. Patent No. 3,223,647 and British Patent 437,566. In general terms, amine oxides are prepared by the controlled oxidation of the corresponding tertiary amines.
  • Most preferably, the surfactant will be lauryl dimethyl amine oxide. The amine oxide surfactant is present in the amount of 2.0-8.0% by weight of the total composition.
  • The composition can contain other optional components appropriate to limescale removing compositions including dyes and fragrances.
  • The balance of the composition of the invention (to 100 weight percent) is deionized water.
  • The composition of the invention is dispensable through a conventional foam dispenser.
  • Modes for Carrying Out the Invention
  • Exemplary compositions of the invention are now set out below:
  • Example 1
  • Material % w/w
    Deionized Water To balance
    Xanthan gum with altered rheology (Kelco) 0.50
    Sulphamic Acid (GelpKe and Bate Ltd.) 10.00
    Citric Acid 4.00
    Lauryl dimethyl amine oxide 2.00
    1% Dye Solution - Blue 0.50
    Fragrance 0.10
  • Example 2
  • Material % w/w
    Deionized Water To balance
    Xanthan gum with altered rheology (Kelco) 0.70
    Sulphamic Acid (GelpKe and Bate Ltd.) 9.00
    Lactic Acid (Purac®) 5.00
    Lauryl dimethyl amine oxide 4.00
    1% Dye Solution - Blue 0.30
    Fragrance 0.20
  • Example 3
  • Material % w/w
    Deionized Water To balance
    Xanthan gum with altered rheology (Kelco) 0.60
    Sulphamic Acid (GelpKe and Bate Ltd.) 13.00
    Lactic Acid (Purac®) 1.00
    Lauryl dimethyl amine oxide 5.00
    1% Dye Solution Acid Blue 7 0.40
    Fragrance 0.10
  • The composition of Example 3 had a viscosity of 250 cps and on dispensing through a conventional foam dispenser produced a foam with a cling parameter of 50 - 70% over a 5 minute period.
  • The composition was stable on storage at room temperature for one year.
  • The composition of Example 3 was tested for effectiveness by the marble cube test as follows:
  • Marble Cube Test
  • 1) 3 marble cubes weighing approximately 20g were washed with distilled water and dried in an oven until their weight was constant at room temperature.
  • 2) Each marble cube was weighed (Wo).
  • 3) 150g of product being tested was weighed into a conical flask.
  • 4) The pre-weighed marble cubes were placed into the test product.
  • 5) The marble cubes were left on test for 18 hours.
  • 6) After 18 hours, the marble cubes were removed from the test product and rinsed thoroughly with deionized water.
  • 7) Each marble cube was dried in an oven for 12 hours and weighed at room temperature. (W1)
  • The percentage descaling was calculated as follows: W0 - W1 x 100% = % weight loss.
  • Interpretation of Results
  • The higher the percentage weight loss the greater the limescale removal activity of the product.
  • Results of the above Marble Cube Test
  • For the composition of Example 3, the average % weight loss (for the 3 cubes) ranged from 35 - 40%.
  • Comparative Example 1
  • A commercially available maleic acid limescale removing composition was tested in the same way as above and the % weight loss ranged from 20 - 30%.
  • Industrial Applicability
  • The subject invention provides a limescale removing composition which may be produced using conventional manufacturing methods and packaging. The foamable limescale removing composition maintains its foaming and rheological properties after shelf storage at room temperature for 6 months, preferably one year. This shelf stability will allow a consumer to effectively utilize the descaling composition even though the composition may be placed into its final package a long time prior to its purchase and use.

Claims (9)

  1. An aqueous liquid storage-stable foamable limescale removing composition consisting of:
    a. from 5% to 20% by weight of a mixture of sulphamic acid and an organic carboxylic acid;
    b. from 0.001% to 5% by weight of a thickening agent selected from acrylic emulsion polymer thickeners, xanthan gums, rhamsan gums, welan gums and polyurethane;
    c. from 2% to 8% by weight of an amine oxide surfactant;
    d. optionally a dye;
    e. optionally a fragrance; and
    f. deionized water to balance;
       wherein the viscosity of the composition is 300 cps or less, the viscosity being measured using a Brookfield viscometer at 20°C using #3 spindle at 30 rpm.
  2. The composition of Claim 1 wherein the viscosity of the composition is in the range of 200 cps to 300 cps, the viscosity being measured using a Brookfield viscometer at 20°C using #3 spindle at 30 rpm..
  3. The composition of Claim 1 wherein the composition has a cling parameter of 50% to 70%, wherein the cling parameter is determined by spraying an amount of the composition onto the underside of a suspended plate and after 5 minutes re-weighing the plate and the composition clinging to the plate.
  4. The composition of Claim 1 wherein the organic carboxylic acid is selected from the group consisting of lactic acid, citric acid, hydroxy acids where the hydroxy group is alpha to at least one of the acid moieties, and mixtures thereof.
  5. The composition of Claim 1 wherein the amine oxide surfactant is an alkyl amine oxide surfactant.
  6. The composition of Claim 5 wherein the alkyl amine oxide surfactant is a C10 to C16 alkyl dimethyl amine oxide.
  7. The composition of Claim 6 wherein the alkyl amine oxide surfactant is lauryl dimethyl amine oxide.
  8. An aqueous liquid storage stable foamable limescale removing composition consisting of:
    5% to 20% by weight of a mixture of sulphamic acid and an organic carboxylic acid selected from the group consisting of lactic acid, citric acid, hydroxy acids where the hydroxy group is alpha to at least one of the acid moieties, and mixtures thereof;
    0.001% to 5% by weight of a thickening agent selected from the group consisting of acrylic emulsion polymers, xanthan gums, rhamsan gums, welan gums and polyurethane;
    2% to 8% by weight of an amine oxide surfactant;
    optionally a dye;
    optionally a fragrance;
       wherein the balance of the composition is deionized water, and
       wherein the viscosity of the composition is 300 cps or less, the viscosity being measured using a Brookfield viscometer at 20°C using # 3 spindle et 30 rpm.
  9. A method of removing limescale from a substrate comprising the steps of:
    applying the composition of any of the preceding claims to a substrate containing limescale;
    allowing the composition to remain in contact with the substrate for a sufficient amount of time to have a descaling effect; and
    removing the composition from the substrate.
EP96944872A 1996-01-03 1996-12-19 Cleaning compositions Expired - Lifetime EP0813585B1 (en)

Applications Claiming Priority (3)

Application Number Priority Date Filing Date Title
GBGB9600030.2A GB9600030D0 (en) 1996-01-03 1996-01-03 Cleaning compositions
GB9600030 1996-01-03
PCT/US1996/020219 WO1997025401A1 (en) 1996-01-03 1996-12-19 Cleaning compositions

Publications (2)

Publication Number Publication Date
EP0813585A1 EP0813585A1 (en) 1997-12-29
EP0813585B1 true EP0813585B1 (en) 2002-03-27

Family

ID=10786532

Family Applications (1)

Application Number Title Priority Date Filing Date
EP96944872A Expired - Lifetime EP0813585B1 (en) 1996-01-03 1996-12-19 Cleaning compositions

Country Status (12)

Country Link
EP (1) EP0813585B1 (en)
KR (1) KR19980702727A (en)
CN (1) CN1181105A (en)
AT (1) ATE215121T1 (en)
AU (1) AU713065B2 (en)
BR (1) BR9607812A (en)
CA (1) CA2214524A1 (en)
DE (1) DE69620158T2 (en)
DK (1) DK0813585T3 (en)
ES (1) ES2170887T3 (en)
GB (1) GB9600030D0 (en)
WO (1) WO1997025401A1 (en)

Families Citing this family (12)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
EP0919610B1 (en) * 1997-10-31 2005-03-16 The Procter & Gamble Company Liquid acidic limescale removal compositions packaged in a spray-type dispenser
US6333299B1 (en) 1997-10-31 2001-12-25 The Procter & Gamble Co. Liquid acidic limescale removal composition packaged in a spray-type dispenser
US5895781A (en) * 1997-12-22 1999-04-20 S. C. Johnson & Son, Inc. Cleaning compositions for ceramic and porcelain surfaces and related methods
FR2841802B1 (en) * 2002-07-08 2005-03-04 Commissariat Energie Atomique COMPOSITION, FOAM AND METHOD FOR DECONTAMINATING SURFACES
US20040229763A1 (en) * 2003-02-28 2004-11-18 The Procter & Gamble Company Cleaning kit and/or a dishwashing kit containing a foam-generating dispenser and a cleaning and/or dishwashing composition
CN1753985A (en) * 2003-02-28 2006-03-29 宝洁公司 A cleaning kit and/or a dishwashing kit containing a foam-generating dispenser and a cleaning and/or dishwashing composition
US7402554B2 (en) 2003-02-28 2008-07-22 The Procter & Gamble Company Foam-generating kit containing a foam-generating dispenser and a composition containing a high level of surfactant
KR20050106051A (en) * 2003-02-28 2005-11-08 더 프록터 앤드 갬블 캄파니 Foam-generating kit containing a foam-generating dispenser and a composition containing a high level of surfactant
US7651992B2 (en) 2003-02-28 2010-01-26 The Procter & Gamble Company Foam-generating kit containing a foam-generating dispenser and a composition containing a high level of surfactant
DE102004020017A1 (en) * 2004-04-21 2005-11-17 Henkel Kgaa Strongly acidic sanitary cleaner with stabilized viscosity and phase behavior
JP4732115B2 (en) * 2005-10-14 2011-07-27 花王株式会社 Acid detergent composition for hard surfaces
CN110498867B (en) * 2018-05-17 2021-08-03 中国石油化工股份有限公司 Modified welan gum, preparation method thereof, water-based fracturing fluid composition and water-based fracturing fluid

Family Cites Families (5)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
GB1240469A (en) * 1967-08-08 1971-07-28 Atlas Preservative Company Ltd Improvements in or relating to cleaning compositions
FR2469450A1 (en) * 1979-11-12 1981-05-22 Solitaire Produits Entretien F Aq. aerosol descaling and cleaning compsn. - contg. organic acid, surfactant, gelling agent and hygroscopic agent
US4587030A (en) * 1983-07-05 1986-05-06 Economics Laboratory, Inc. Foamable, acidic cleaning compositions
KR950006289B1 (en) * 1986-07-17 1995-06-13 알 앤드 시 프로덕츠 피티와이. 리미티드 Amine-acid thickening compositions
DE69327846T2 (en) * 1993-11-29 2000-10-26 Procter & Gamble Scale removal compositions

Also Published As

Publication number Publication date
ES2170887T3 (en) 2002-08-16
AU713065B2 (en) 1999-11-25
AU1337497A (en) 1997-08-01
DK0813585T3 (en) 2002-07-08
DE69620158D1 (en) 2002-05-02
CN1181105A (en) 1998-05-06
GB9600030D0 (en) 1996-03-06
ATE215121T1 (en) 2002-04-15
BR9607812A (en) 1998-07-07
KR19980702727A (en) 1998-08-05
CA2214524A1 (en) 1997-07-17
DE69620158T2 (en) 2002-08-14
WO1997025401A1 (en) 1997-07-17
EP0813585A1 (en) 1997-12-29

Similar Documents

Publication Publication Date Title
US5707952A (en) Thickened acid composition
US5008030A (en) Acidic disinfectant all-purpose liquid cleaning composition
EP0813585B1 (en) Cleaning compositions
JP3001980B2 (en) Aqueous composition for rinsing shower equipment and method for keeping shower equipment clean
EP2260094B1 (en) Use of citrate as cleaning aid for hard surfaces
US7368417B2 (en) Hard surface cleaning compositions comprising a lauryl hydroxysultaine
EP1313833B2 (en) Cleaning aid
CA2047085A1 (en) Hard surface liquid cleaning composition with soil release polymer
CA2106329A1 (en) Thickened acid microemulsion composition
US6153572A (en) Acidic liquid toilet bowl cleaner
CN101160384B (en) Liquid hard surface cleaning composition
US6420329B1 (en) Cleaning compositions
EP0648834B1 (en) Carpet cleaner
EP1478722B1 (en) Liquid cleaning compositions
PL174150B1 (en) Improvement in general purpose cleaning compositions
JPH0873890A (en) Liquid detergent composition for hard surface cleaning
JPH11510542A (en) Acidic cleaning composition
JPH07118689A (en) Cleaning agent composition for hard surface
JP5106786B2 (en) Detergent composition for dishwasher
MXPA97006712A (en) Limpi compositions
JPH07305100A (en) Acidic microemulsion composition
JP2017078129A (en) Bathroom liquid detergent
JP3013758B2 (en) Liquid detergent composition
CN112673082A (en) Fast and easy cleaning formulation

Legal Events

Date Code Title Description
PUAI Public reference made under article 153(3) epc to a published international application that has entered the european phase

Free format text: ORIGINAL CODE: 0009012

17P Request for examination filed

Effective date: 19970904

AK Designated contracting states

Kind code of ref document: A1

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

17Q First examination report despatched

Effective date: 19991213

GRAG Despatch of communication of intention to grant

Free format text: ORIGINAL CODE: EPIDOS AGRA

GRAG Despatch of communication of intention to grant

Free format text: ORIGINAL CODE: EPIDOS AGRA

GRAH Despatch of communication of intention to grant a patent

Free format text: ORIGINAL CODE: EPIDOS IGRA

GRAH Despatch of communication of intention to grant a patent

Free format text: ORIGINAL CODE: EPIDOS IGRA

REG Reference to a national code

Ref country code: GB

Ref legal event code: IF02

GRAA (expected) grant

Free format text: ORIGINAL CODE: 0009210

AK Designated contracting states

Kind code of ref document: B1

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

PG25 Lapsed in a contracting state [announced via postgrant information from national office to epo]

Ref country code: LI

Free format text: LAPSE BECAUSE OF FAILURE TO SUBMIT A TRANSLATION OF THE DESCRIPTION OR TO PAY THE FEE WITHIN THE PRESCRIBED TIME-LIMIT

Effective date: 20020327

Ref country code: GR

Free format text: LAPSE BECAUSE OF FAILURE TO SUBMIT A TRANSLATION OF THE DESCRIPTION OR TO PAY THE FEE WITHIN THE PRESCRIBED TIME-LIMIT

Effective date: 20020327

Ref country code: FI

Free format text: LAPSE BECAUSE OF FAILURE TO SUBMIT A TRANSLATION OF THE DESCRIPTION OR TO PAY THE FEE WITHIN THE PRESCRIBED TIME-LIMIT

Effective date: 20020327

Ref country code: CH

Free format text: LAPSE BECAUSE OF FAILURE TO SUBMIT A TRANSLATION OF THE DESCRIPTION OR TO PAY THE FEE WITHIN THE PRESCRIBED TIME-LIMIT

Effective date: 20020327

Ref country code: AT

Free format text: LAPSE BECAUSE OF FAILURE TO SUBMIT A TRANSLATION OF THE DESCRIPTION OR TO PAY THE FEE WITHIN THE PRESCRIBED TIME-LIMIT

Effective date: 20020327

REF Corresponds to:

Ref document number: 215121

Country of ref document: AT

Date of ref document: 20020415

Kind code of ref document: T

REG Reference to a national code

Ref country code: CH

Ref legal event code: EP

REF Corresponds to:

Ref document number: 69620158

Country of ref document: DE

Date of ref document: 20020502

REG Reference to a national code

Ref country code: IE

Ref legal event code: FG4D

PG25 Lapsed in a contracting state [announced via postgrant information from national office to epo]

Ref country code: SE

Free format text: LAPSE BECAUSE OF FAILURE TO SUBMIT A TRANSLATION OF THE DESCRIPTION OR TO PAY THE FEE WITHIN THE PRESCRIBED TIME-LIMIT

Effective date: 20020627

Ref country code: PT

Free format text: LAPSE BECAUSE OF FAILURE TO SUBMIT A TRANSLATION OF THE DESCRIPTION OR TO PAY THE FEE WITHIN THE PRESCRIBED TIME-LIMIT

Effective date: 20020627

REG Reference to a national code

Ref country code: DK

Ref legal event code: T3

REG Reference to a national code

Ref country code: ES

Ref legal event code: FG2A

Ref document number: 2170887

Country of ref document: ES

Kind code of ref document: T3

REG Reference to a national code

Ref country code: CH

Ref legal event code: PL

PG25 Lapsed in a contracting state [announced via postgrant information from national office to epo]

Ref country code: LU

Free format text: LAPSE BECAUSE OF NON-PAYMENT OF DUE FEES

Effective date: 20021219

Ref country code: IE

Free format text: LAPSE BECAUSE OF NON-PAYMENT OF DUE FEES

Effective date: 20021219

PGFP Annual fee paid to national office [announced via postgrant information from national office to epo]

Ref country code: ES

Payment date: 20030109

Year of fee payment: 7

PLBE No opposition filed within time limit

Free format text: ORIGINAL CODE: 0009261

STAA Information on the status of an ep patent application or granted ep patent

Free format text: STATUS: NO OPPOSITION FILED WITHIN TIME LIMIT

26N No opposition filed

Effective date: 20021230

REG Reference to a national code

Ref country code: IE

Ref legal event code: MM4A

PG25 Lapsed in a contracting state [announced via postgrant information from national office to epo]

Ref country code: ES

Free format text: LAPSE BECAUSE OF NON-PAYMENT OF DUE FEES

Effective date: 20031220

PGFP Annual fee paid to national office [announced via postgrant information from national office to epo]

Ref country code: NL

Payment date: 20041129

Year of fee payment: 9

PGFP Annual fee paid to national office [announced via postgrant information from national office to epo]

Ref country code: DK

Payment date: 20041228

Year of fee payment: 9

PGFP Annual fee paid to national office [announced via postgrant information from national office to epo]

Ref country code: BE

Payment date: 20050119

Year of fee payment: 9

REG Reference to a national code

Ref country code: ES

Ref legal event code: FD2A

Effective date: 20031220

PG25 Lapsed in a contracting state [announced via postgrant information from national office to epo]

Ref country code: IT

Free format text: LAPSE BECAUSE OF NON-PAYMENT OF DUE FEES;WARNING: LAPSES OF ITALIAN PATENTS WITH EFFECTIVE DATE BEFORE 2007 MAY HAVE OCCURRED AT ANY TIME BEFORE 2007. THE CORRECT EFFECTIVE DATE MAY BE DIFFERENT FROM THE ONE RECORDED.

Effective date: 20051219

PG25 Lapsed in a contracting state [announced via postgrant information from national office to epo]

Ref country code: BE

Free format text: LAPSE BECAUSE OF NON-PAYMENT OF DUE FEES

Effective date: 20051231

PG25 Lapsed in a contracting state [announced via postgrant information from national office to epo]

Ref country code: DK

Free format text: LAPSE BECAUSE OF NON-PAYMENT OF DUE FEES

Effective date: 20060102

PG25 Lapsed in a contracting state [announced via postgrant information from national office to epo]

Ref country code: NL

Free format text: LAPSE BECAUSE OF NON-PAYMENT OF DUE FEES

Effective date: 20060701

REG Reference to a national code

Ref country code: DK

Ref legal event code: EBP

NLV4 Nl: lapsed or anulled due to non-payment of the annual fee

Effective date: 20060701

PGFP Annual fee paid to national office [announced via postgrant information from national office to epo]

Ref country code: FR

Payment date: 20061220

Year of fee payment: 11

PGFP Annual fee paid to national office [announced via postgrant information from national office to epo]

Ref country code: DE

Payment date: 20070131

Year of fee payment: 11

BERE Be: lapsed

Owner name: S.C. *JOHNSON & SON INC.

Effective date: 20051231

PGFP Annual fee paid to national office [announced via postgrant information from national office to epo]

Ref country code: GB

Payment date: 20071227

Year of fee payment: 12

PG25 Lapsed in a contracting state [announced via postgrant information from national office to epo]

Ref country code: DE

Free format text: LAPSE BECAUSE OF NON-PAYMENT OF DUE FEES

Effective date: 20080701

REG Reference to a national code

Ref country code: FR

Ref legal event code: ST

Effective date: 20081020

PG25 Lapsed in a contracting state [announced via postgrant information from national office to epo]

Ref country code: FR

Free format text: LAPSE BECAUSE OF NON-PAYMENT OF DUE FEES

Effective date: 20071231

GBPC Gb: european patent ceased through non-payment of renewal fee

Effective date: 20081219

PG25 Lapsed in a contracting state [announced via postgrant information from national office to epo]

Ref country code: GB

Free format text: LAPSE BECAUSE OF NON-PAYMENT OF DUE FEES

Effective date: 20081219