WO1998049257A1 - Compositions acides eliminant le tartre - Google Patents

Compositions acides eliminant le tartre Download PDF

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Publication number
WO1998049257A1
WO1998049257A1 PCT/IB1998/000644 IB9800644W WO9849257A1 WO 1998049257 A1 WO1998049257 A1 WO 1998049257A1 IB 9800644 W IB9800644 W IB 9800644W WO 9849257 A1 WO9849257 A1 WO 9849257A1
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Prior art keywords
acid
alkyl
composition
group
compositions
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PCT/IB1998/000644
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English (en)
Inventor
Luigi Pace
Alberto Caselli
Giulia Ottavia Bianchetti
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The Procter & Gamble Company
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Priority to JP54677598A priority Critical patent/JP2001522305A/ja
Priority to CA002287835A priority patent/CA2287835A1/fr
Publication of WO1998049257A1 publication Critical patent/WO1998049257A1/fr

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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
    • C11D3/02—Inorganic compounds ; Elemental compounds
    • C11D3/04—Water-soluble compounds
    • C11D3/042—Acids
    • 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
    • C11D1/88—Ampholytes; Electroneutral compounds
    • C11D1/94—Mixtures with anionic, cationic or non-ionic compounds
    • 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
    • C11D3/20—Organic compounds containing oxygen
    • C11D3/2075—Carboxylic acids-salts thereof
    • C11D3/2082—Polycarboxylic acids-salts thereof
    • 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
    • C11D3/34—Organic compounds containing sulfur
    • C11D3/3418—Toluene -, xylene -, cumene -, benzene - or naphthalene sulfonates or sulfates
    • 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
    • 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
    • C11D1/22—Sulfonic acids or sulfuric acid esters; Salts thereof derived from aromatic compounds
    • 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
    • C11D1/22—Sulfonic acids or sulfuric acid esters; Salts thereof derived from aromatic compounds
    • C11D1/24—Sulfonic acids or sulfuric acid esters; Salts thereof derived from aromatic compounds containing ester or ether groups directly attached to the nucleus
    • 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
    • C11D1/29—Sulfates of polyoxyalkylene ethers
    • 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
    • C11D1/88—Ampholytes; Electroneutral compounds
    • C11D1/90—Betaines
    • 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
    • C11D3/34—Organic compounds containing sulfur
    • C11D3/3409—Alkyl -, alkenyl -, cycloalkyl - or terpene sulfates or sulfonates

Definitions

  • the present invention relates to liquid acidic self-thickened compositions designed for optimum performance in removing limescale.
  • Tap water contains a certain amount of solubilized ions which upon water evaporation eventually deposit as salts such as calcium carbonate on surfaces which are often in contact with water, resulting in an unaesthetic aspect of the surfaces. This limescale formation and deposition phenomenon is even more acute in places where water is particularly hard.
  • liquid acidic limescale removal compositions do not perform equally well on all limescale-containing stains, particularly on limescale-containing stains which can be found in bathrooms or in kitchens, i.e., on stains containing mineral deposits like calcium and/or magnesium carbonate but also high amount of organic deposits such as greasy soap scum, i.e. soap scum and other greasy soils typically occuring in daily usage of bathrooms, e.g. body soils, and/or greasy soils typically occuring in daily usage of kitchens. Indeed, the presence of such greasy soap scum is detrimental to the limescale removal performance of conventional acidic compositions.
  • viscous compositions are desired, there are some drawbacks associated with product viscosity. And a main drawback is that viscous compositions are typically difficult to rinse away because they have a good cling onto surfaces. Thus, viscosity and ease of rinsing are somewhat conflicting requirements, but both are desirable in a single composition for removing limescale deposits from hard surfaces.
  • a zwitterionic surfactant preferably a sulfobetaine surfactant, as a primary surfactant
  • an anionic surfactant preferably a primary or secondary C6-C20 alkyl sulphonate and/or a primary or secondary C6-C20 a'M ar Y' sulphonates
  • improved thickening properties are delivered to said composition while being nevertheless easy to rinse away.
  • the present invention allows to use low level of total thickening surfactants to achieve a given viscosity.
  • a lower total level of thickening surfactants i.e., zwitterionic surfactants and anionic surfactants
  • zwitterionic surfactants and anionic surfactants are sufficient in the present invention, as compared to the level of other self-thickening systems like for example nonionic surfactant systems required to get the same thickening effect.
  • the acidic compositions of the present invention comprising a zwitterionic surfactant and an anionic surfactant in the appropriate ratios as described herein but these compositions also deliver improved limescale removal performance and improved greasy soap scum cleaning performance.
  • the presence of the zwitterionic surfactants, especially sulfobetaine surfactants, as the primary surfactant in the acidic limescale removal compositions of the present invention provides improved limescale removal performance and inhibit soap scum deposition on a surface first treated with such a composition, ensuring thereby long lasting soap scum cleaning to said surface.
  • the acidic liquid thickened compositions according to the present invention exhibit excellent chemical and physical stability.
  • a further advantage of the present invention is that the liquid thickened compositions herein are translucent, as opposed to clouded, and thus well accepted from a consumer view point. Also, the present invention allows to formulate compositions that are Newtonian. By “Newtonian”, it is meant herein a composition which has the same viscosity whichever applied shear stress, as opposed to “pseudoplastic” compositions, i.e. thickened compositions whose viscosity depends on the shear stress applied. Thus, a benefit of the present invention is that this thickening system leads to newtonian compositions whose effectiveness in removing limescale from hard surfaces does not depend on whether the surface is inclined or horizontal.
  • compositions of the present invention have a much lower yield value, i.e. the minimum shear stress required to have the composition start flowing, than pseudoplastic compositions. This means that the compositions of the present invention spread over the surface to be treated more uniformly, thus requiring less product per unit area to be treated and resulting thereby in a higher product effectiveness/quantity ratio.
  • the preferred acidic compositions of the present invention comprising maleic acid together with a second acid typically sulfamic acid are effective limescale removal compositions while being safe to various surfaces including metal surfaces such as aluminium, chromed steel or stainless steel as well as synthetic materials and to the user skin.
  • GB 2071 688 discloses liquid acidic compositions comprising an inorganic acid and as a thickening agent a mixture of an amine or amine oxide with a cationic or nonionic surfactant. No anionic surfactants and no zwitterionic surfactants are disclosed.
  • EP-A-265 979 discloses acidic thickened aqueous cleaning compositions comprising a disinfecting and/or oxidising agent, an organic anionic sulphonate selected from the group consisting of xylene sulphonate, cumene sulphonate and toluene sulphonate, and a surfactant selected from the group of (1 ) quaternary ammonium compounds wherein at least one of the hydrocarbon groups linked to the nitrogen is a linear or branched alkyl group containing at least 12 carbon atoms and of (2) tertiary amine oxides wherein at least one of the hydrocarbon groups linked to the nitrogen is a linear or branched alkyl group containing at least 1 6 carbon atoms.
  • the present invention uses zwitterionic surfactants like betaine and/or sulfobetaine surfactants together with anionic surfactants in a weight ratio of the zwitterionic surfactant to the anionic surfactant of at least 2: 1 , as the thickening system.
  • EP-A-188 025 discloses aqueous stable thickened low-pH bleaching compositions comprising an inorganic peroxy compound, a strong acid and a thickening surfactant.
  • the compositions are said to have a viscosity of 10 to 250 m Pa s.
  • the thickening surfactant is selected from (1 ) amine oxides wherein at least one of the hydrocarbon groups linked to the nitrogen is a linear or branched alkyl group of C6 to C18 carbon atoms, preferably C12 to C18, (2) amines and (3) quaternary ammonium salts wherein at least one of the hydrocarbon groups linked to the nitrogen is a linear or branched alkyl group of C8 to C18 carbon atoms.
  • EP-A-188 025 teaches to use as a thickening surfactant one of these thickening surfactants.
  • No acidic compositions comprising as a thickening system, a zwitterionic surfactant, e.g. a sulfobetaine and/or a betaine surfactant, together with an anionic surfactant at a weight ratio of the zwitterionic surfactant to the anionic surfactant of at least 2: 1 is disclosed.
  • compositions according to the present invention are liquid acidic thickened compositions having a viscosity of at least 10 m Pa s, when measured with a Carri-med rheometer at 5 N/m 2 at 20°C and a pH below 4, said composition comprising a thickening system comprising a zwitterionic surfactant and an anionic surfactant at a weight ratio of said zwitterionic surfactant to said anionic surfactant of at least 2:1 , and from 0.1 % to 70% by weight of the total composition of an acid or a mixture thereof.
  • the present invention also encompasses a process of treating a hard- surface, wherein a liquid thickened composition according to the present invention, is applied in its neat or diluted form onto said surface, optionally left to act thereto for an effective period of time and then removed.
  • a liquid thickened composition according to the present invention is applied in its neat or diluted form onto said surface, optionally left to act thereto for an effective period of time and then removed.
  • the liquid thickened compositions according to the present invention are preferably aqueous compositions. Therefore, they comprise from 50% to 98% by weight of the total composition of water, preferably from 60% to 95% and more preferably from 70% to 90%.
  • One of the achievements of the present invention is that the viscosity build up described hereinafter can be achieved with such a high amount of water, i.e., a small amount of actives.
  • compositions of the present invention are acidic compositions. Accordingly, the compositions of the present invention are formulated at a pH below 4, preferably at a pH between 0 and 3, more preferably at a pH between 0.1 and 2.5, even more preferably between 0.1 and 2, and most preferably at a pH between 0.3 and 1 .5.
  • compositions according to the present invention are designed for removing limescale deposits.
  • they comprise as a first essential ingredient an acid or a mixture thereof.
  • the acids to be used herein may be any inorganic or organic acid well-known to those skilled in the art, or a mixture thereof.
  • Suitable acids for use herein include maleic acid, citric acid, adipic acid, sulfamic acid, phosphoric acid, nitric acid, malic acid, sulfonic acid, sulphuric acid or their salts or mixtures thereof.
  • such acids can be used in their acidic form or in the form of their salts (mono-, di-, tri- salts) and in all their anhydrous and hydrated forms, or mixtures thereof.
  • Such acids may typically be used in the form of their alkali metal salts (e.g. sodium salt, potassium salt, and then like) or their alkali hydrogen acid salts.
  • Said compositions comprise from 0.1 % to 70% by weight of the total composition of an acid or a mixture thereof.
  • compositions of the present invention comprise at least maleic acid.
  • the compositions according to the present invention comprise from 0.1 % to 45% by weight of the total composition of maleic acid, preferably from 1 % to 25% and more preferably from 8% to 20%. This percentage is calculated on the basis of the molecular weight of the acid form, but maleic anhydride is equally convenient for use in the compositions according to the present invention. Indeed, maleic anhydride is generally cheaper and it is transformed into the acid form when incorporated in an aqueous medium. In one embodiment of the present invention maleic acid is used alone as the acid of the acidic compositions of the present invention.
  • a second acid is added on top of said maleic acid.
  • Said second acid is desired to strengthen the limescale removal performance.
  • the second acids to be used herein which are particularly efficient to remove limescale on many surfaces, have their first pKa not exceeding 5, more preferably not exceeding 3, and most preferably not exceeding 2.
  • said acids can be organic or inorganic acids.
  • sulphamic acid Particularly suitable to be used herein is sulphamic acid. Indeed, it has now been found that the addition of sulphamic acid on top of maleic acid in the compositions of the present invention improves the skin mildness of said compositions. Indeed, less skin irritation is perceived by the user when its skin comes into contact with these compositions as compared to the same compositions but without sulphamic acid.
  • Suitable second acids are sulphonic acid derivatives including alkyl sulphonic acids and aryl sulphonic acids.
  • Suitable aryl sulphonic acids for use herein are according to the formula
  • R- ⁇ R2, R3, R4 and R5 are each H or SO3H, or linear or branched C1 -C4 alkyl chain; or mixtures thereof.
  • Preferred acids having a first pKa not exceeding 5 to be used herein are sulphamic acid, sulphuric acid, aryl sulphonic acids, alkyl sulphonic acids, or mixtures thereof, more preferred are sulphamic acid, sulphuric acid, benzene sulphonic acid or mixtures thereof and highly preferred is sulphamic acid.
  • compositions of the present invention comprise from 0.1 % to 25% by weight of the total composition of a second acid which has a first pKa not exceeding 5, or mixtures thereof, preferably from 0.1 % to 20%, more preferably from 0.1 % to 10% and most preferably from 0.1 % to 7%.
  • compositions according to the present invention comprise as a second essential ingredient a surfactant system comprising a zwitterionic surfactant and an anionic surfactant at a weight ratio of the zwitterionic surfactant to the anionic surfactant of at least 2: 1 , preferably at least 3: 1 , more preferably from 10: 1 to 3: 1 , even more preferably from 8: 1 to 3:1 and most preferably from 6: 1 to 3.5: 1 .
  • a zwitterionic surfactant with an anionic surfactant as described herein at a weight ratio of the zwitterionic surfactant to the anionic surfactant of at least 2: 1 , in an acidic composition comprising an acid or a mixture thereof, a viscosity of at least 10 m Pa s, is obtained, when measured with a Carri-med rheometer at 5 N/m2 at 20°C, with a 4 cm diameter cone spindle, while exhibiting excellent physical and chemical stability.
  • compositions according to the present invention are chemically stable.
  • chemically stable it is meant herein that chemical parameters such as composition pH and/or acidity reserve do not change when the composition is stored in rapid aging test (RAT) at 50 °C for 6 days.
  • RAT rapid aging test
  • liquid acidic thickened compositions according to the present invention are physically stable.
  • physically stable it is meant herein that neither phase separation nor viscosity changes occur when the composition is stored in rapid aging test (RAT) at 50 °C for 3 days or at 2 °C for 2 weeks.
  • RAT rapid aging test
  • compositions of the present invention typically have a viscosity of from 10 m Pa s to 1000 m Pa s at 20°C, preferably from 10 m Pa s to 400 m Pa s, more preferably from 20 m Pa s to 200 m Pa s, and most preferably from 30 m Pa s to 1 50 m Pa s, when measured with a Carrimed rheometer CLS 100® by TA Instruments at 5 N/m2 with a 4 cm diameter cone spindle.
  • the present invention allows to use low level of total thickening surfactants to achieve a given viscosity.
  • the total level of thickening surfactants i.e., of zwitterionic surfactants and anionic surfactants, to be used in a given acidic liquid composition depends on the thickness desired for said composition.
  • the total level of thickening surfactants is lower than 20%, preferably between 0.5% and 8%, more preferably between 1 % and 5%, and most preferably between 1 % and 3.5%.
  • Suitable zwitterionic surfactants to be used herein contain at least one anionic and one cationic group in the molecule.
  • the typical cationic group can be a secondary or tertiary ammonium group (so called "weak nitrogen zwitterionics") or a quaternary ammonium group (so called "betaines”), although other positively charged groups like phosphonium, imidazolium and sulfonium groups can be used.
  • betaines carry a positive charge over the whole pH range
  • weak nitrogen zwitterionics carry a positive charge only in acidic pH.
  • the typical anionic hydrophilic groups are carboxylates and sulfonates, although other groups like sulfates, phosphonates, and the like can be used.
  • a generic formula for preferred zwitterionic surfactants to be used herein i.e., betaine and/or sulfobetaine is :
  • R-j is a hydrophobic group
  • R 2 is hydrogen, Ci -C ⁇ alkyl, hydroxy alkyl or other substituted C-i -C ⁇ alkyl group
  • R3 is C-i -C ⁇ alkyl, hydroxy alkyl or other substituted ⁇ -CQ alkyl group which can also be joined to R 2 to form ring structures with the N, or a Ci -C ⁇ carboxylic acid group or a C1 -C5 sulfonate group
  • R4 is a moiety joining the cationic nitrogen atom to the hydrophilic group and is typically an alkylene, hydroxy alkylene, or polyalkoxy group containing from 1 to 10 carbon atoms
  • X is the hydrophilic group which is a carboxylate or sulfonate group, preferably a sulfonate group.
  • are aliphatic or aromatic, saturated or unsaturated, substituted or unsubstituted hydrocarbon chains that can contain linking groups such as amido groups, ester groups. More preferred R-
  • the hydrophobic group R-i can also be an amido radical of the formula R a -C(O)-NRbJC(R c )2)m' wher ein R a is a ⁇ aliphatic or aromatic, saturated or unsaturated, substituted or unsubstituted hydrocarbon chain containing from 8 up to 20 carbon atoms, preferably an alkyl group containing from 8 up to 20 carbon atoms, preferably up to 18, more preferably up to 16, R D is either a hydrogen or a short chain alkyl or substituted alkyl containing from 1 to 4 carbon atoms, preferably a group selected from the group consisting of methyl, ethyl, propyl, hydroxy substituted ethyl or propyl and mixtures thereof, more preferably methyl or hydrogen, R c is selected from the group consisting of hydrogen and hydroxy groups, and m is from 1 to 4, preferably from 2 to 3, more preferably 3, with no more than one hydroxy group in any (C(R C ) )
  • Preferred R 2 is hydrogen, or an alkyl or substituted alkyl containing from 1 to 4 carbon atoms, preferably a group selected from the group consisting of methyl, ethyl, propyl, hydroxy substituted ethyl or propyl and mixtures thereof, more preferably methyl.
  • Preferred R3 is a C1 -C4 carboxylic acid group, a C1 -C4 sulfonate group, or an alkyl or substituted alkyl containing from 1 to 4 carbon atoms, preferably a group selected from the group consisting of methyl, ethyl, propyl, hydroxy substituted ethyl or propyl and mixtures thereof, more preferably methyl.
  • Preferred R4 is (CH2) n wherein n is an integer from 1 to 10, preferably from 1 to 6, more preferably from 1 to 3.
  • betaine/sulphobetaine Some common examples of betaine/sulphobetaine are described in U.S. Pat. Nos. 2,082,275, 2,702,279 and 2,255,082, incorporated herein by reference.
  • alkyldimethyl betaines examples include coconut- dimethyl betaine, lauryl dimethyl betaine, decyl dimethyl betaine, 2-(N- decyl-N, N-dimethyl-ammonia)acetate, 2-(N-coco N, N- dimethylammonio) acetate, myristyl dimethyl betaine, palmityl dimethyl betaine, cetyl dimethyl betaine, stearyl dimethyl betaine.
  • coconut dimethyl betaine is commercially available from Seppic under the trade name of Amonyl 265®.
  • Lauryl betaine is commercially available from Albright & Wilson under the trade name Empigen BB/L®.
  • betaine Lauryl-immino-dipropionate commercially available from Rhone-Poulenc under the trade name Mirataine H2C-HA
  • Particularly preferred zwitterionic surfactants to be used in the acidic compositions of the present invention are the sulfobetaine surfactants, as they deliver optimum limescale removal benefits, soap scum cleaning benefits and thickening benefits.
  • sulfobetaine surfactants include tallow bis(hydroxyethyl) sulphobetaines and cocoamido propyl hydroxy sulfobetaines which are commercially available from Rhone Poulenc and Witco, under the trade name of Mirataine CBS® and Rewoteric AM CAS 1 5® respectively.
  • amidobetaines/sulfobetaines include cocoamidoethylbetaine, cocoamidopropyl betaine or C10-C14 fatty acylamidopropylene(hydropropylene)sulfobetaine.
  • C10-C14 fatty acylamidopropylene(hydropropylene)sulfobetaine is commercially available from Sherex Company under the trade name "Varion CAS® sulfobetaine".
  • compositions according to the present invention comprise from 0.01 % to 20% by weight of the total composition of a zwitterionic surfactant or mixtures thereof, preferably from 0.1 % to 10% and most preferably from 0.5% to 5%.
  • Suitable anionic surfactants to be used herein as the cosurfactant include primary and secondary Ce-C 2 o alkyl sulphonates, primary and secondary C5-C20 alkyl aryl sulphonates, C6-C20 alkyl sulphates, Cg-
  • C20 alkyl alkoxylated sulphates C -C20 alkyl alkoxylated linear or branched diphenyl oxide disulphonates or other conventional anionic surfactants as mentioned herein after or mixtures thereof, preferably primary and secondary Cg-C20 alkyl sulphonates, primary and secondary Cg-C20 alkyl aryl sulphonates, Cg-C 2 o alkyl sulphates, Cg-
  • C20 alkyl alkoxylated sulphates C -C20 alkyl alkoxylated linear or branched diphenyl oxide disulphonates or mixtures thereof and more preferably primary and secondary Cg-C20 alky' sulphonates, primary and secondary Cg-C20 alkyl aryl sulphonates or a mixture thereof.
  • Suitable alkyl sulphonates to be used herein include water-soluble salts or acids of the formula RSO3M wherein R is a Cg-C20 linear or branched, saturated or unsaturated alkyl group, preferably a C ⁇ 2 -C-
  • RSO3M where
  • Suitable alkyl aryl sulphonates to be used herein include water- soluble salts or acids of the formula RSO3M wherein R is an aryl, preferably a benzyl, substituted by a Cg-C 2 o linear or branched saturated or unsaturated alkyl group, preferably a C-
  • secondary C6-C20 alkyl or C6-C20 alkyl aryl sulphonates it is meant herein that in the formula as defined above, the SO3M or aryl- SO3M group is linked to a carbon atom of the alkyl chain being placed between two other carbons of the said alkyl chain (secondary carbon atom).
  • C14-C1 6 alkyl sulphonate is Hostapur ® SAS available from Hoechst.
  • An example of commercially available alkyl aryl sulphonate is Lauryl aryl sulphonate from Su.Ma.
  • Particularly preferred alkyl aryl sulphonates are alkyl benzene sulphonates commercially available under trade name Nansa® available from Albright&Wilson.
  • Suitable alkyl sulphate surfactants for use herein are according to the formula R1 SO4M wherein R-
  • M is H or a cation, e.g., an alkali metal cation (e.g., sodium, potassium, lithium, calcium, magnesium etc) or ammonium or substituted ammonium (e.g., methyl-, dimethyl-, and trimethyl ammonium cations and quaternary ammonium cations, such as tetramethyl-ammonium and dimethyl piperdinium cations and quaternary ammonium cations derived from alkylamines such as ethylamine, diethylamine, triethylamine, and mixtures thereof, and the like).
  • an alkali metal cation e.g., sodium, potassium, lithium, calcium, magnesium etc
  • ammonium or substituted ammonium e.g., methyl-, dimethyl-, and trimethyl ammonium cations and quaternary ammonium cations, such as tetramethyl-ammonium and dimethyl piperdinium cations and quatern
  • Suitable alkyl alkoxylated sulphate surfactants for use herein are according to the formula RO(A) m SO3M wherein R is an unsubstituted Cg-C 2 0 alkyl or hydroxyalkyi group having a C -C20 alkyl component, preferably a C ⁇ -C 2 o a " cy ' or hydroxyalkyi, more preferably C ⁇ 2 -C-
  • R is an unsubstituted Cg-C 2 0 alkyl or hydroxyalkyi group having a C -C20
  • Alkyl ethoxylated sulfates as well as alkyl propoxylated sulfates are contemplated herein.
  • Specific examples of substituted ammonium cations include methyl-, dimethyl-, trimethyl-ammonium and quaternary ammonium cations, such as tetramethyl-ammonium, dimethyl piperdinium and cations derived from alkanolamines such as ethylamine, diethylamine, triethylamine, mixtures thereof, and the like.
  • Exemplary surfactants are C-
  • Suitable Cg-C20 alkyl alkoxylated linear or branched diphenyl oxide disulphonate surfactants for use herein are according to the following formula:
  • R is a Cg-C20 linear or branched, saturated or unsaturated alkyl group, preferably a C ⁇ 2 -C 18 a,k y' ⁇ Joup and more preferably a C-
  • X + is H or a cation, e.g., an alkali metal cation (e.g., sodium, potassium, lithium, calcium, magnesium etc).
  • Particularly suitable Cg-C 2 Q alkyl alkoxylated linear or branched diphenyl oxide disulphonate surfactants to be used herein are the C1 2 branched di phenyl oxide disulphonic acid and C16 linear di phenyl axide disulphonate sodium salt respectively commercially available by DOW under the trade name Dowfax 2A1 ® and Dowfax 8390®.
  • anionic surfactants useful herein include salts (including, for example, sodium, potassium, ammonium, and substituted ammonium salts such as mono-, di- and triethanolamine salts) of soap, Cs-C 2 4 olefinsulfonates, sulfonated polycarboxylic acids prepared by sulfonation of the p ⁇ rolyzed product of alkaline earth metal citrates, e.g., as described in British patent specification No.
  • alkylpolyglycolethersulfates (containing up to 10 moles of ethylene oxide); alkyl ester sulfonates such as Ci 4_ ⁇ g methyl ester sulfonates; acyl glycerol sulfonates, fatty oleyl glycerol sulfates, alkyl phenol ethylene oxide ether sulfates, alkyl phosphates, isethionates such as the acyl isethionates, N-acyl taurates, alkyl succinamates and sulfosuccinates, monoesters of sulfosuccinate (especially saturated and unsaturated C-
  • Resin acids and hydrogenated resin acids are also suitable, such as rosin, hydrogenated rosin, and resin acids and hydrogenated resin acids present in or derived from tall oil. Further examples are given in "Surface Active Agents and Detergents" (Vol. I and II by Schwartz, Perry and Berch). A variety of such surfactants are also generally disclosed in U.S. Patent 3,929,678, issued December 30, 1975 to Laughlin, et al. at Column 23, line 58 through Column 29, line 23.
  • compositions of the present invention comprise from 0.001 % to 10% by weight of the total composition of said anionic surfactant or mixtures thereof, preferably from 0.01 % to 3%, more preferably from 0.1 % to 1 .5% and most preferably from 0.2% to 1 %.
  • the self thickened surfactant system according to the present invention allows to lower the surface tension and to improve the wettability of the surfaces being cleaned with the liquid acidic compositions of the present invention.
  • the presence of said surfactant system in the liquid acidic compositions of the present invention helps to solubilize the soils.
  • the addition, in an acidic liquid composition, of the surfactant system according to the present invention, i.e., a zwitterionic surfactant, as the primary surfactant, and a small amount of an anionic surfactant, as the co-surfactant, provides improved greasy soap scum cleaning performance as well as improved limescale removal performance, as compared to the greasy soap scum cleaning performance and limescale removal performance obtained with the same composition but with another surfactant system like for instance combination of nonionic surfactants, e.g. alcohol ethoxylate surfactants, instead of said surfactant system, this even at significantly lower total surfactant level.
  • the zwitterionic surfactants as described herein act as lime soap dispersing agent.
  • Ca cations coming from tap water are complexed by soap itself leading to formation of "soap scum” (also called “lime soap”, i.e., insoluble organic calcium salts such as calcium stearate or calcium oleate) which precipitates.
  • a lime soap dispersing agent is a compound that allows, thanks to its large head group, the formation of mixed micelles with soap molecules, thus avoiding formation and then precipitation of insoluble organic calcium salts.
  • a zwitterionic surfactant as defined herein, preferably sulfobetaine surfactant, in a liquid acidic composition reduces or even prevents deposition of soap scum on a hard-surface after the surface has been first treated with said composition, thereby ensuring long lasting soap scum cleaning benefit.
  • compositions according to the present invention may further comprise a variety of other ingredients including other surfactants, colorants, bactericides, polymers, dyes, chelants, pigments, solvents, stabilizers, perfumes, corrosion inhibitors and the like.
  • the compositions herein exhibit the desired viscosity due to the presence of the surfactant system described hereinbefore without the presence of a polymer.
  • the compositions of the present invention may further comprise a charged polymer (i.e., a polymer which has either a positive or a negative charge when incorporated in the acidic compositions of the present invention).
  • a charged polymer i.e., a polymer which has either a positive or a negative charge when incorporated in the acidic compositions of the present invention.
  • the addition of the polymer contributes to the formation of high micelle packing by the surfactant system that results in viscosity build up in the acidic compositions herein.
  • the addition of charged polymer exposing a charged backbone, in the acidic compositions of the present invention further enhances the surfactant system ability to form very tightly packed micelles and thus to increase the viscosity of the compositions.
  • Suitable polymers to be used herein including polycarboxylate polymers, sulphonated polystyrene polymers, vinylpyrrolidone homopolymer or copolymers, polyalkoxylene glycols, polysaccharide polymers or a mixture thereof.
  • Suitable polycarboxylate polymers for use herein are polymers comprising monomeric units selected from the group consisting of unsaturated carboxylic acids such as acrylic acid, polycarboxylic acids, sulphonic acids, phosphonic acids and mixtures thereof.
  • Copolymerisation of the above monomeric units among them or with other co-monomers such as maleic anhydride, ethylene or propylene are also suitable.
  • maleic anhydride will acts as a source of additional carboxylic groups, whilst ethylene and propylene will act as diluents.
  • the molecular weight per carboxylate group of monomers containing a carboxylate group typically varies from 20 to 200, preferably from 40 to 1 50, more preferably from 50 to 1 25.
  • Preferred polymers for use herein have a total molecular weight of from 2,000 to 4,500,000, preferably from 10,000 to 4,000,000.
  • Most preferred 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 polycarboxylate polymers for use herein are the polyacrylate polymers.
  • acrylic/maleic-based copolymers may be used as a preferred polyacrylate polymer.
  • Such materials include the water- soluble salts of copolymers of acrylic acid and maleic acid.
  • the average molecular weight of such copolymers in the acid form preferably ranges from about 2,000 to 1 ,000,000, more preferably from about 5,000 to 100,000, most preferably from about 10,000 to 80,000.
  • the ratio of acrylate to maleate segments in such copolymers will generally range from about 30:1 to about 1 : 1 , more preferably from about 10: 1 to 2: 1 .
  • Water-soluble salts of such acrylic acid/maleic acid copolymers can include, for example, the alkali metal, ammonium and substituted ammonium salts.
  • Soluble acrylate/maleate copolymers of this type are known materials which are described in European Patent Application No. 6691 5, published December 1 5, 1982. Particularly preferred is a copolymer of maleic / acrylic acid with an average molecular weight of about 70,000.
  • Such copolymers are commercially available from BASF under the trade name Sokalan CP5®.
  • polyacrylate polymers are the copolymer of acrylic acid and alkyl (C5-C10) acrylate, commercially available under the tradename Carbopol® 1 623, Carbopol® 695 from BF Goodrich.
  • Commercially available polymers of the polyacrylate type further include those sold under the trade names Carbopol®, Acrysol® ICS-1 , Polygel®, and Sokalan®.
  • the first type is a sulfonated homopolymer of styrene.
  • the second type is a sulfonated interpolymer of styrene with an ethylenically unsaturated comonomer.
  • the useful compounds herein include the partially or fully neutralized salts of either the sulfonated polystyrene or the sulfonated styrene interpolymers, i.e. the soluble salts of these polymers, wherein the sulfonic acid groups are partially or fully neutralized.
  • Suitable ethylenically unsaturated comonomer units which can be copolymerized with styrene to make the interpolymers suitable for sulfation include acrylic and methacrylic esters of aliphatic alcohols such as methyl, ethyl, butyl and 2-ethyl hexyl alcohols, acrylic acid, acrylonitrile, methacrylonitrile, dibutyl maleate, vinylidene chloride and the like.
  • Particularly preferred ethylenically unsaturated monomers for use herein include ethylene, propylene, styrene, vinyl naphthalene, acrylic acid and maleic anhydride.
  • Sulphonated styrene homopolymers suitable for use herein are commercially available under the trade name Versaflex® from National Starch. Most suitable polymers and copolymers for use herein will be water soluble, and the molecular weight for these polymers is preferably between 5000 and 10,000,000, most preferably between 50,000 and 1 ,000,000.
  • Suitable vinylpyrrolidone homopolymers to be used herein are homopolymers of N-vinylpyrrolidone having the following repeating monomer:
  • n degree of polymerisation
  • PVP vinylpyrrolidone homopolymers
  • Suitable vinylpyrrolidone homopolymers are commercially available from ISP Corporation, New York, NY and Montreal, Canada under the product names PVP K-1 5® (viscosity molecular weight of 10,000), PVP K-30® (average molecular weight of 40,000), PVP K-60® (average molecular weight of 1 60,000), and PVP K-90® (average molecular weight of 360,000).
  • Other suitable vinylpyrrolidone homopolymers which are commercially available from BASF Cooperation include Sokalan HP 1 65® and Sokalan HP 1 2®; vinylpyrrolidone homopolymers known to persons skilled in the detergent field (see for example EP-A-262,897 and EP-A- 256,696).
  • Suitable copolymers of vinylpyrrolidone for use herein include copolymers of N-vinylpyrrolidone and alkylenically unsaturated monomers or mixtures thereof.
  • the alkylenically unsaturated monomers of the copolymers herein include unsaturated dicarboxylic acids such as maleic acid, chloromaleic acid, fumaric acid, itaconic acid, citraconic acid, phenylmaleic acid, aconitic acid, acrylic acid, N-vinylimidazole and vinyl acetate. Any of the anhydrides of the unsaturated acids may be employed, for example acrylate, methacrylate. Aromatic monomers like styrene, sulphonated styrene, alpha-methyl styrene, vinyl toluene, t-butyl styrene and similar well known monomers may be used.
  • the molecular weight of the copolymer of vinylpyrrolidone is not especially critical so long as the copolymer is water-soluble, has some surface activity and is adsorbed to the hard-surface from the liquid composition or solution (i.e. under dilute usage conditions) comprising it in such a manner as to increase the hydrophilicity of the surface.
  • the preferred copolymers of N-vinylpyrrolidone and alkylenically unsaturated monomers or mixtures thereof have a molecular weight of between 1 ,000 and 1 ,000,000, preferably between 10,000 and 500,000 and more preferably between 10,000 and 200,000.
  • N-vinylimidazole N-vinylpyrrolidone polymers for use herein have an average molecular weight range from 5,000-1 ,000,000, preferably from 5,000 to 500,000, and more preferably from 10,000 to 200,000.
  • the average molecular weight range was determined by light scattering as described in Barth H.G. and Mays J.W. Chemical Analysis Vol 1 13, "Modern Methods of Polymer Characterization".
  • Such copolymers of N-vinylpyrrolidone and alkylenically unsaturated monomers like PVP/vinyl acetate copolymers are commercially available under the trade name Luviskol® series from BASF.
  • copolymers of vinylpyrrolidone for use in the compositions of the present invention also include quaternized or unquaternized vinylpyrrolidone/dialkylaminoalkyl acrylate or methacrylate copolymers.
  • the preferred quaternized or unquaternized vinylpyrrolidone/dialkylaminoalkyl acrylate or methacrylate copolymers for use herein have a molecular weight of between 1 ,000 and 1 ,000,000, preferably between 10,000 and 500,000 and more preferably between 10,000 and 100,000.
  • Such vinylpyrrolidone/dialkylaminoalkyl acrylate or methacrylate copolymers are commercially available under the name copolymer 845®, Gafquat 734®, or Gafquat 755® from ISP Corporation, New York, NY and Montreal, Canada or from BASF under the tradename Luviquat®.
  • Suitable polyalkoxylene glycols to be used herein have the following formula :
  • R is hydrogen or a linear or branched hydrocarbon chain having from 1 to 30 carbon atoms, preferably R is hydrogen, or a linear or branched alkyl group, alkenyl group or aryl group having from 1 to 30 carbon atoms, more preferably from 1 to 1 6, even more preferably from 1 to 8, and most preferably R2 is methyl, or hydrogen.
  • n is an integer from 5 to 1000, more preferably from 10 to 100, even more preferably from 20 to 60 and most preferably from 30 to 50.
  • the preferred polyalkoxylene glycols to be used according to the present invention have a molecular weight of at least 200, more preferably from 400 to 5000 and most preferably from 800 to 3000.
  • Preferred polyalkoxylene glycols are polyethylene glycols like polyethylene glycol (MW 2000).
  • Suitable polysaccharide polymers for use herein include substituted cellulose materials like carboxymethylcellulose, ethyl cellulose, hydroxyethyl cellulose, hydroxypropyl cellulose, hydroxymethyl cellulose, succinoglycan and naturally occurring polysaccharide polymers like xanthan gum, guar gum, locust bean gum, tragacanth gum or derivatives thereof, or mixtures thereof.
  • Particularly preferred polysaccharide polymers to be used herein are xanthan gum and derivatives thereof.
  • Xanthan gum and derivatives thereof may be commercially available for instance from Kelco under the trade name Keltrol RD®, Kelzan S® or Kelzan T®.
  • Preferred acid-stable polymers to be used herein are the sulphonated polystyrene polymers and/or the vinylpyrrolidone homopolymers.
  • compositions according to the present invention may comprise up to 3% by weight of the total composition of a polymer or mixture thereof preferably up to 1 %, more preferably from 0.001 % to 1 % and most preferably from 0.01 % to 0.5%
  • compositions according to the present invention may further comprise other surfactants apart the surfactant system described hereinbefore.
  • the compositions according to the present invention may comprise up to 30% by weight of the total composition of said other surfactant or mixtures thereof on top of the surfactant system of the present invention, more preferably from 0.05% to 10%, more preferably from 0.1 % to 8%, and most preferably from 0.1 % to 3%.
  • All types of surfactants may be used in the present invention including nonionic, anionic, cationic or amphoteric surfactants. It is also possible to use mixtures of such surfactants without departing from the spirit of the present invention.
  • Suitable nonionic surfactants to be used herein are alkoxylated alcohol nonionic surfactants which can be readily made by condensation processes which are well-known in the art. However, a great variety of such alkoxylated alcohols, especially ethoxylated and/or propoxylated alcohols is also conveniently commercially available. Surfactants catalogs are available which list a number of surfactants, including nonionics.
  • preferred alkoxylated alcohols for use herein are nonionic surfactants according to the formula RO(E)e(P)pH where R is a hydrocarbon chain of from 2 to 24 carbon atoms, E is ethylene oxide and P is propylene oxide, and e and p which represent the average degree of, respectively ethoxylation and propoxylation, are of from 0 to 24.
  • the hydrophobic moiety of the nonionic compound can be a primary or secondary, straight or branched alcohol having from 8 to 24 carbon atoms.
  • Preferred nonionic surfactants for use in the compositions according to the invention are the condensation products of ethylene oxide with alcohols having a straight alkyl chain, having from 6 to 22 carbon atoms, wherein the degree of ethoxylation is from 1 to 1 5, preferably from 5 to 12.
  • Such suitable nonionic surfactants are commercially available from Shell, for instance, under the trade name Dobanol® or from Shell under the trade name Lutensol®- These nonionics are preferred because they have been found to allow the formulation of a stable product without requiring the addition of stabilisers or hydrotopes.
  • Suitable amine oxides to be used herein are according to the following formula R1 R2R3NO wherein each of R1 , R2 and R3 is independently a saturated or unsaturated, substituted or unsubstituted, linear or branched alkyl group containing from 1 to 30 carbon atoms, and preferably from 1 to 20 carbon atoms.
  • Particularly preferred amine oxides to be used according to the present invention are amine oxides having the following formula R1 R2R3NO wherein R1 is a saturated or unsaturated, substituted or unsubstituted, linear or branched alkyl group containing from 1 to 30 carbon atoms, preferably from 8 to 20 carbon atoms, more preferably from 6 to 16, most preferably from 8 to 14, and wherein R2 and R3 are independently substituted or unsubstituted, linear or branched alkyl groups of from 1 to 4 carbon atoms, preferably from 1 to 3 carbon atoms, and more preferably are methyl groups, or mixtures thereof.
  • Suitable amine oxides for use herein are for instance coconut dimethyl amine oxides, C12-C1 6 dimethyl amine oxides. Said amine oxides may be commercially available from Hoechst, Stephan, AKZO (under the trade name Aromox®) or FINA (under the trade name Radiamox®).
  • Suitable amines to be used herein are according to the following formula RR'R"N wherein R is a saturated or unsaturated, substituted or unsubstituted, linear or branched alkyl group containing from 1 to 30 carbon atoms, and preferably from 1 to 20 carbon atoms and wherein R' and R" are independently saturated or unsaturated, substituted or unsubstituted, linear or branched alkyl groups containing from 1 to 30 carbon atoms or hydrogen.
  • Particularly preferred amines to be used according to the present invention are amines having the following formula RR'R"N wherein R is a saturated or unsaturated, linear or branched alkyl group containing from 1 to 30 carbon atoms, preferably from 8 to 20 carbon atoms, more preferably from 6 to 16, most preferably from 8 to 14 and wherein R' and R" are independently substituted or unsubstituted, linear or branched alkyl groups containing from 1 to 4 carbon atoms, preferably from 1 to 3 carbon atoms, and more preferably are methyl groups, or mixtures thereof.
  • Suitable amines for use herein are for instance C1 2 dimethyl amine, coconut dimethyl amine, C12-C1 6 dimethyl amine. Said amines may be commercially available from Hoechst under the trade name Genamin®, AKZO under the trade name Aromox® or Fina under the trade name Radiamox®.
  • Suitable cationic surfactants to be used herein include derivatives of quaternary ammonium, phosphonium, imidazolium and sulfonium compounds.
  • Preferred cationic surfactants for use herein are according to the formula R-
  • is a C10-C1 8 hydrocarbon chain, most preferably C-J 2' Cl 4,» or C"l g, an ⁇ ⁇ 2> ⁇ 3 ap R4 are all three methyl, and X can be hydroxyl, methylsulphate or halogen, preferably bromide or chloride, most preferably bromide.
  • cationic surfactants are lauryl trimethyl ammonium bromide, stearyl trimethyl ammonium bromide (STAB), cetyl trimethyl ammonium bromide (CTAB) and myristyl trimethyl ammonium bromide (MTAB). Highly preferred herein are lauryl trimethyl ammonium salts.
  • the liquid compositions according to the present invention may be colored. Accordingly, they may comprise a dye or a mixture thereof.
  • Suitable dyes to be used herein are acid-stable dyes. By “acid-stable” it is meant herein a compound which is chemically and physically stable in the acidic environment of the compositions herein.
  • Suitable dyes to be used herein include ⁇ or ⁇ metal phthalocyanines and/or trimethyl methane dyes.
  • the ⁇ or ⁇ metal phthalocyanine dyes suitable to be used in the compositions of the present invention are light-fast organic pigments with four isoindole groups, (C H4>C2 , linked by four nitrogen atoms to form a conjugated chain.
  • Their general structure is the following:
  • substituent X may be one of the following groups : H, Cl, HSO3, COO-M + , Br, NO2, OCH3 or a C1 to C10 a ' k yl group and where Me is copper, chromium, vanadium, magnesium, nickel, platinum, aluminium, cobalt, lead, barium or zinc.
  • Preferred ⁇ or ⁇ metal phthalocyanine dyes to be used herein are ⁇ or ⁇ copper phthalocyanine dyes.
  • trimethyl methane dyes are commercially available from Hoescht under the name Vitasyn® or from BASF under the name Acid Blue®.
  • compositions of the present invention may comprise up to 0.2% by weight of the total composition of a dye or a mixture thereof, preferably from 0.001 % to 0.01 5% and more preferably from 0.001 % to 0.012%.
  • liquid acidic thickened compositions of the present invention may be packaged in a variety of suitable detergent packaging known to those skilled in the art.
  • the acidic liquid compositions of the present invention comprising an acid and the self- thickening surfactant system herein may be easily dispensed onto the surface to be treated via a spray-type dispenser such as for instance a trigger-sprayer.
  • a spray-type dispenser such as for instance a trigger-sprayer.
  • the present invention also encompasses liquid compositions of the invention packaged in a spray dispenser, preferably in a trigger spray dispenser or in a pump spray dispenser.
  • 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 ,31 1 to Dunnining et al. and US-4,646,973 and US-4,538,745 both to Focarracci. Particularly preferred to be used herein are spray- type dispensers such as T 8500® or T 8900® commercially available from Continental Spray International or T 8100® commercially available from Canyon, Northen 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.
  • the composition contained in the body of said dispenser is directed through the spray-type dispenser head via energy communicated to a pumping mechanism 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.
  • an obstacle e.g. a grid or a cone or the like
  • a further advantage of the present invention is that the acidic liquid compositions of the present invention may be applied uniformly to a relatively large area of a surface to be treated via a spray-type dispenser, thereby ensuring improved limescale removal performance and improved greasy soap scum cleaning performance.
  • compositions according to the present invention may be manufactured by adding the different ingredients in any order. However, the desired initial viscosity of an aqueous composition of the present invention is obtained immediately, when following a preferred mixing order for the incorporation of the different ingredients in said composition. Accordingly, the present invention further encompasses a process for manufacturing the liquid acidic thickened compositions of the present invention, wherein said process comprises the steps of first preparing a water acidic solution with the desired pH by mixing the acids with water and then adding the other ingredients in the following order:
  • the primary surfactant i.e. the zwitterionic surfactant
  • compositions according to the present invention are particularly suitable for treating hard-surfaces soiled by limescale-containing stains.
  • limescale-containing stains it is meant herein any pure limescale stains, i.e., any stains composed essentially of mineral deposits as well as limescale-containing stains typically found, for example, in a kitchen or in a bathroom, i.e., stains which contain not only mineral deposits like calcium and/or magnesium carbonate but also soap scum (e.g., calcium stearate) and other grease.
  • compositions of the present invention exhibit excellent limescale removing performance when used to treat any types of surfaces soiled by limescale-containing stains comprising not only pure limescale deposits but also at least 10% by weight of the total stain of organic deposits like soap scum and grease, preferably more than 30%.
  • surfaces can be found in bathrooms, kitchens, but also in appliances including large appliances such as automatic dish washers and/or washing machines.
  • the present invention encompasses a process of treating hard-surfaces soiled by limescale-containing stains wherein an aqueous acidic liquid composition according to the present invention is applied in its neat form or in diluted form, onto said surfaces, then left to act onto said surfaces and then removed by rinsing.
  • the expression "used in diluted form” herein includes dilution by the user. Typical dilution levels are of from 0.5% to 50% by weight of the composition.
  • treating includes removing limescale deposits while being safe to the surfaces treated as well as cleaning greasy soap scum stains due to the presence of said surfactant system.
  • the limescale removal capacity of a composition according to the present invention may be evaluated by soaking a marble block (marble blocks are chemically speaking very similar to limescale, i.e. they are essentially made of calcium carbonate) into 20 g of this composition. The marble is weighed before and after the experiment, and the performance is expressed in grams of marble block dissolved over time. Alternatively, limescale removal performance can also be evaluated by detecting the release of CO2.
  • enamel white tiles (typically 24 cm * 4 cm) are covered with typical greasy soap scum soils mainly based on calcium stearate and artificial body soils commercially available (e.g. 0.3 grams with a sprayer).
  • the soiled tiles are then dried in an oven at a temperature of 140 °C for 30 minutes and then aged overnight at room temperature (around 1 5°C-20°C).
  • the soiled tiles are treated with a Spontex® sponge impregnated with the liquid acidic composition of the present invention (e.g. 5 grams).
  • the ability of the composition to remove greasy soap scum is measured through the number of strokes needed to perfectly clean the surface. The lower the number of strokes, the higher the greasy soap scum cleaning ability of the composition.
  • an arbitrary amount of lime soap dispersing agent e.g. 5 ml of 0.25g/100ml solution
  • % lime soap dispersing ability A ( in grams) x 100 0.025 (weight of sodium oleate)
  • compositions were made comprising the listed ingredients in the listed proportions (weight %).
  • Viscosity 100 1 10 80 140 90 45 (mPasM* ** *)
  • Mirataine CBS® and Rewoteric AM CAS® 15 are examples of cocoamidopropyl hydroxy sulphobetaine supplied respectively by Rhone- Poulenc and Witco.
  • HLAS is Linear alkyl benzene sulphonate in acid form while Na LAS is its sodium salt.
  • Hostapur SAS® is a secondary alkane sulphonate supplied by Hoechst (* * * *) Viscosity grows with time; therefore, those are the value measured just after product making, i.e., they are the lowest achievable viscosities with the above indicated compositions.
  • the initial viscosity of the above compositions were measured by a Carri-Med Rheomoter CLS 100® by TA instruments at fixed shear stress of 5 N/m 2 at 20°C with a 4 cm diameter cone spindle. 50 N/m 2 as shear stress value is representative of a fluid flow occurring on an inclined surface when the product thickness on the surface is about 1 mm and the only external force is due to the gravity field.
  • compositions according to the present invention are translucent, Newtonian compositions that provide significant benefits in limescale removal applications. Indeed, all the compositions of the above examples exhibit excellent limescale removal performance as well as outstanding greasy soap scum cleaning performance when used to clean limescale-containing stains found in a kitchen and in a bathroom, this both when used neat or in diluted form. These compositions also ensure long lasting soap scum cleaning to the surface having been treated therewith.

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Abstract

Cette invention concerne des compositions acides, liquides et épaissies qui possèdent une viscosité d'au moins 10 mPa s, telle que mesurée à l'aide d'un rhéomètre Carrimed à 5 N/m2 et à une température de 20 °C, et un pH inférieur à 4. Cette composition contient un système épaississant qui comprend un tensioactif zwittérionique et un tensioactif anionique, ceci selon un rapport en poids du tensioactif zwittérionique par rapport au tensioactif anionique d'au moins 2:1. Cette composition comprend également de 0,1 à 70 % d'un acide par rapport à son poids total. Ces compositions offrent d'excellentes capacités d'élimination du tartre ainsi qu'une étonnante capacité de nettoyage de résidus de savon gras sur des surfaces dures. Ces compositions conviennent au nettoyage de surfaces horizontales ou non horizontales.
PCT/IB1998/000644 1997-04-30 1998-04-24 Compositions acides eliminant le tartre WO1998049257A1 (fr)

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US9062280B2 (en) 2009-08-06 2015-06-23 Arkema Inc. Liquid cleaning composition
WO2020109022A1 (fr) * 2018-11-30 2020-06-04 Unilever N.V. Compositions de nettoyage conservées
US11490618B2 (en) 2018-06-04 2022-11-08 Conopco, Inc. Preservation compositions
US11684557B2 (en) 2018-06-04 2023-06-27 Conopco, Inc. Preservation compositions
US11872296B2 (en) 2018-06-04 2024-01-16 Conopco, Inc. Preservation compositions

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EP1566431A1 (fr) * 2004-02-23 2005-08-24 The Procter & Gamble Company Détergent lessiviel comprenant un tensioactif anionique et d'acide sulfamique et/ou son sel
GT200600375A (es) * 2005-08-17 2007-03-14 Composición limpiadora ácida que contiene un polímero de hidrofilización
FR2897611B1 (fr) * 2006-02-20 2008-05-30 Gilles Allard Produit de traitement d'un reservoir et d'une cuvette de chasse d'eau
FR2898067B1 (fr) * 2006-03-03 2008-05-30 Rhodia Recherches & Tech Modification de surfaces solides par des associations de polymeres
WO2014056906A1 (fr) * 2012-10-11 2014-04-17 Henkel Ag & Co. Kgaa Détergents auto-épaississants
JP5972749B2 (ja) * 2012-10-18 2016-08-17 オルガノ株式会社 スケール洗浄液組成物およびスケール洗浄方法

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EP2462215A4 (fr) * 2009-08-06 2016-04-27 Arkema Inc Compositions de nettoyage liquides
US11490618B2 (en) 2018-06-04 2022-11-08 Conopco, Inc. Preservation compositions
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EP0875551A1 (fr) 1998-11-04
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