AU723832B2 - Improvements relating to limescale removing compositions - Google Patents
Improvements relating to limescale removing compositions Download PDFInfo
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- AU723832B2 AU723832B2 AU27725/97A AU2772597A AU723832B2 AU 723832 B2 AU723832 B2 AU 723832B2 AU 27725/97 A AU27725/97 A AU 27725/97A AU 2772597 A AU2772597 A AU 2772597A AU 723832 B2 AU723832 B2 AU 723832B2
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- 239000000203 mixture Substances 0.000 title claims description 52
- 235000014113 dietary fatty acids Nutrition 0.000 claims description 24
- 239000000194 fatty acid Substances 0.000 claims description 24
- 229930195729 fatty acid Natural products 0.000 claims description 24
- 150000004665 fatty acids Chemical class 0.000 claims description 23
- KDYFGRWQOYBRFD-UHFFFAOYSA-N succinic acid Chemical compound OC(=O)CCC(O)=O KDYFGRWQOYBRFD-UHFFFAOYSA-N 0.000 claims description 20
- NBIIXXVUZAFLBC-UHFFFAOYSA-N Phosphoric acid Chemical compound OP(O)(O)=O NBIIXXVUZAFLBC-UHFFFAOYSA-N 0.000 claims description 18
- OFOBLEOULBTSOW-UHFFFAOYSA-N Malonic acid Chemical compound OC(=O)CC(O)=O OFOBLEOULBTSOW-UHFFFAOYSA-N 0.000 claims description 13
- WNLRTRBMVRJNCN-UHFFFAOYSA-N adipic acid Chemical compound OC(=O)CCCCC(O)=O WNLRTRBMVRJNCN-UHFFFAOYSA-N 0.000 claims description 12
- 239000001384 succinic acid Substances 0.000 claims description 10
- 229910000147 aluminium phosphate Inorganic materials 0.000 claims description 9
- 239000003945 anionic surfactant Substances 0.000 claims description 9
- -1 secondary alcohol sulphates Chemical class 0.000 claims description 9
- RTBFRGCFXZNCOE-UHFFFAOYSA-N 1-methylsulfonylpiperidin-4-one Chemical compound CS(=O)(=O)N1CCC(=O)CC1 RTBFRGCFXZNCOE-UHFFFAOYSA-N 0.000 claims description 7
- JFCQEDHGNNZCLN-UHFFFAOYSA-N anhydrous glutaric acid Natural products OC(=O)CCCC(O)=O JFCQEDHGNNZCLN-UHFFFAOYSA-N 0.000 claims description 7
- 150000001991 dicarboxylic acids Chemical class 0.000 claims description 7
- 235000011037 adipic acid Nutrition 0.000 claims description 6
- 239000001361 adipic acid Substances 0.000 claims description 5
- QAOWNCQODCNURD-UHFFFAOYSA-L Sulfate Chemical compound [O-]S([O-])(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-L 0.000 claims description 4
- 238000007046 ethoxylation reaction Methods 0.000 claims description 4
- 229910021653 sulphate ion Inorganic materials 0.000 claims description 4
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 claims description 3
- 239000003960 organic solvent Substances 0.000 claims description 3
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical group [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 claims description 2
- 125000003545 alkoxy group Chemical group 0.000 claims description 2
- 150000003138 primary alcohols Chemical class 0.000 claims description 2
- 239000002253 acid Substances 0.000 description 24
- 239000000047 product Substances 0.000 description 11
- 150000007513 acids Chemical class 0.000 description 10
- 235000011044 succinic acid Nutrition 0.000 description 9
- 239000002585 base Substances 0.000 description 8
- 238000001556 precipitation Methods 0.000 description 7
- 238000004140 cleaning Methods 0.000 description 5
- RTZKZFJDLAIYFH-UHFFFAOYSA-N ether Substances CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 description 5
- 238000009472 formulation Methods 0.000 description 5
- 239000002304 perfume Substances 0.000 description 4
- 239000004094 surface-active agent Substances 0.000 description 4
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 4
- QTDIEDOANJISNP-UHFFFAOYSA-N 2-dodecoxyethyl hydrogen sulfate Chemical compound CCCCCCCCCCCCOCCOS(O)(=O)=O QTDIEDOANJISNP-UHFFFAOYSA-N 0.000 description 3
- HEMHJVSKTPXQMS-UHFFFAOYSA-M Sodium hydroxide Chemical compound [OH-].[Na+] HEMHJVSKTPXQMS-UHFFFAOYSA-M 0.000 description 3
- 229920002125 Sokalan® Polymers 0.000 description 3
- KRKNYBCHXYNGOX-UHFFFAOYSA-N citric acid Chemical compound OC(=O)CC(O)(C(O)=O)CC(O)=O KRKNYBCHXYNGOX-UHFFFAOYSA-N 0.000 description 3
- 230000007797 corrosion Effects 0.000 description 3
- 238000005260 corrosion Methods 0.000 description 3
- 239000003112 inhibitor Substances 0.000 description 3
- 230000002427 irreversible effect Effects 0.000 description 3
- 239000011976 maleic acid Substances 0.000 description 3
- VZCYOOQTPOCHFL-UPHRSURJSA-N maleic acid group Chemical group C(\C=C/C(=O)O)(=O)O VZCYOOQTPOCHFL-UPHRSURJSA-N 0.000 description 3
- 239000002736 nonionic surfactant Substances 0.000 description 3
- 239000003755 preservative agent Substances 0.000 description 3
- 239000000344 soap Substances 0.000 description 3
- 239000002689 soil Substances 0.000 description 3
- VZCYOOQTPOCHFL-UHFFFAOYSA-N trans-butenedioic acid Natural products OC(=O)C=CC(O)=O VZCYOOQTPOCHFL-UHFFFAOYSA-N 0.000 description 3
- VEXZGXHMUGYJMC-UHFFFAOYSA-N Hydrochloric acid Chemical compound Cl VEXZGXHMUGYJMC-UHFFFAOYSA-N 0.000 description 2
- MUBZPKHOEPUJKR-UHFFFAOYSA-N Oxalic acid Natural products OC(=O)C(O)=O MUBZPKHOEPUJKR-UHFFFAOYSA-N 0.000 description 2
- 230000002378 acidificating effect Effects 0.000 description 2
- 150000001279 adipic acids Chemical class 0.000 description 2
- DMSMPAJRVJJAGA-UHFFFAOYSA-N benzo[d]isothiazol-3-one Chemical compound C1=CC=C2C(=O)NSC2=C1 DMSMPAJRVJJAGA-UHFFFAOYSA-N 0.000 description 2
- 229910052791 calcium Inorganic materials 0.000 description 2
- 239000013078 crystal Substances 0.000 description 2
- 210000003298 dental enamel Anatomy 0.000 description 2
- 239000003599 detergent Substances 0.000 description 2
- POULHZVOKOAJMA-UHFFFAOYSA-N dodecanoic acid Chemical compound CCCCCCCCCCCC(O)=O POULHZVOKOAJMA-UHFFFAOYSA-N 0.000 description 2
- 230000008020 evaporation Effects 0.000 description 2
- 238000001704 evaporation Methods 0.000 description 2
- 229910052500 inorganic mineral Inorganic materials 0.000 description 2
- 239000011707 mineral Substances 0.000 description 2
- 235000010755 mineral Nutrition 0.000 description 2
- 150000007524 organic acids Chemical class 0.000 description 2
- 230000002335 preservative effect Effects 0.000 description 2
- 230000002441 reversible effect Effects 0.000 description 2
- 150000003444 succinic acids Chemical class 0.000 description 2
- OYPRJOBELJOOCE-UHFFFAOYSA-N Calcium Chemical compound [Ca] OYPRJOBELJOOCE-UHFFFAOYSA-N 0.000 description 1
- 235000013162 Cocos nucifera Nutrition 0.000 description 1
- 244000060011 Cocos nucifera Species 0.000 description 1
- 239000005639 Lauric acid Substances 0.000 description 1
- AFCARXCZXQIEQB-UHFFFAOYSA-N N-[3-oxo-3-(2,4,6,7-tetrahydrotriazolo[4,5-c]pyridin-5-yl)propyl]-2-[[3-(trifluoromethoxy)phenyl]methylamino]pyrimidine-5-carboxamide Chemical compound O=C(CCNC(=O)C=1C=NC(=NC=1)NCC1=CC(=CC=C1)OC(F)(F)F)N1CC2=C(CC1)NN=N2 AFCARXCZXQIEQB-UHFFFAOYSA-N 0.000 description 1
- MCMNRKCIXSYSNV-UHFFFAOYSA-N Zirconium dioxide Chemical compound O=[Zr]=O MCMNRKCIXSYSNV-UHFFFAOYSA-N 0.000 description 1
- 239000000654 additive Substances 0.000 description 1
- 230000000996 additive effect Effects 0.000 description 1
- 150000001298 alcohols Chemical class 0.000 description 1
- 239000003513 alkali Substances 0.000 description 1
- 239000011575 calcium Substances 0.000 description 1
- VTYYLEPIZMXCLO-UHFFFAOYSA-L calcium carbonate Substances [Ca+2].[O-]C([O-])=O VTYYLEPIZMXCLO-UHFFFAOYSA-L 0.000 description 1
- 235000010216 calcium carbonate Nutrition 0.000 description 1
- 159000000007 calcium salts Chemical class 0.000 description 1
- 229960004106 citric acid Drugs 0.000 description 1
- 239000003086 colorant Substances 0.000 description 1
- 239000012141 concentrate Substances 0.000 description 1
- 238000002474 experimental method Methods 0.000 description 1
- 239000003925 fat Substances 0.000 description 1
- 150000002311 glutaric acids Chemical class 0.000 description 1
- 239000003752 hydrotrope Substances 0.000 description 1
- 230000000670 limiting effect Effects 0.000 description 1
- 239000007788 liquid Substances 0.000 description 1
- 239000011777 magnesium Substances 0.000 description 1
- 229910052749 magnesium Inorganic materials 0.000 description 1
- ZLNQQNXFFQJAID-UHFFFAOYSA-L magnesium carbonate Chemical class [Mg+2].[O-]C([O-])=O ZLNQQNXFFQJAID-UHFFFAOYSA-L 0.000 description 1
- 239000001095 magnesium carbonate Substances 0.000 description 1
- 235000011160 magnesium carbonates Nutrition 0.000 description 1
- 230000014759 maintenance of location Effects 0.000 description 1
- 239000000463 material Substances 0.000 description 1
- 229910052751 metal Inorganic materials 0.000 description 1
- 239000002184 metal Substances 0.000 description 1
- 150000002739 metals Chemical class 0.000 description 1
- 150000007522 mineralic acids Chemical class 0.000 description 1
- 239000003921 oil Substances 0.000 description 1
- 239000003605 opacifier Substances 0.000 description 1
- 235000005985 organic acids Nutrition 0.000 description 1
- 238000004806 packaging method and process Methods 0.000 description 1
- 229920000642 polymer Polymers 0.000 description 1
- 239000002244 precipitate Substances 0.000 description 1
- 102000004169 proteins and genes Human genes 0.000 description 1
- 108090000623 proteins and genes Proteins 0.000 description 1
- 230000002829 reductive effect Effects 0.000 description 1
- NLJMYIDDQXHKNR-UHFFFAOYSA-K sodium citrate Chemical compound O.O.[Na+].[Na+].[Na+].[O-]C(=O)CC(O)(CC([O-])=O)C([O-])=O NLJMYIDDQXHKNR-UHFFFAOYSA-K 0.000 description 1
- 229960000999 sodium citrate dihydrate Drugs 0.000 description 1
- SUKJFIGYRHOWBL-UHFFFAOYSA-N sodium hypochlorite Chemical compound [Na+].Cl[O-] SUKJFIGYRHOWBL-UHFFFAOYSA-N 0.000 description 1
- 239000002904 solvent Substances 0.000 description 1
- 230000003019 stabilising effect Effects 0.000 description 1
- 239000003381 stabilizer Substances 0.000 description 1
- 150000003627 tricarboxylic acid derivatives Chemical class 0.000 description 1
- 238000010792 warming Methods 0.000 description 1
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
- C11D1/00—Detergent compositions based essentially on surface-active compounds; Use of these compounds as a detergent
- C11D1/02—Anionic compounds
- C11D1/37—Mixtures of compounds all of which are anionic
-
- 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
- C11D1/00—Detergent compositions based essentially on surface-active compounds; Use of these compounds as a detergent
- C11D1/02—Anionic 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
- C11D1/04—Carboxylic acids or 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
- C11D1/00—Detergent compositions based essentially on surface-active compounds; Use of these compounds as a detergent
- C11D1/02—Anionic compounds
- C11D1/12—Sulfonic acids or sulfuric acid esters; Salts thereof
- C11D1/14—Sulfonic acids or sulfuric acid esters; Salts thereof derived from aliphatic hydrocarbons or mono-alcohols
- C11D1/143—Sulfonic acid esters
-
- C—CHEMISTRY; METALLURGY
- C11—ANIMAL OR VEGETABLE OILS, FATS, FATTY SUBSTANCES OR WAXES; FATTY ACIDS THEREFROM; DETERGENTS; CANDLES
- C11D—DETERGENT COMPOSITIONS; USE OF SINGLE SUBSTANCES AS DETERGENTS; SOAP OR SOAP-MAKING; RESIN SOAPS; RECOVERY OF GLYCEROL
- C11D1/00—Detergent compositions based essentially on surface-active compounds; Use of these compounds as a detergent
- C11D1/02—Anionic compounds
- C11D1/12—Sulfonic acids or sulfuric acid esters; Salts thereof
- C11D1/14—Sulfonic acids or sulfuric acid esters; Salts thereof derived from aliphatic hydrocarbons or mono-alcohols
- C11D1/146—Sulfuric acid esters
-
- C—CHEMISTRY; METALLURGY
- C11—ANIMAL OR VEGETABLE OILS, FATS, FATTY SUBSTANCES OR WAXES; FATTY ACIDS THEREFROM; DETERGENTS; CANDLES
- C11D—DETERGENT COMPOSITIONS; USE OF SINGLE SUBSTANCES AS DETERGENTS; SOAP OR SOAP-MAKING; RESIN SOAPS; RECOVERY OF GLYCEROL
- C11D1/00—Detergent compositions based essentially on surface-active compounds; Use of these compounds as a detergent
- C11D1/02—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
Landscapes
- Chemical & Material Sciences (AREA)
- Oil, Petroleum & Natural Gas (AREA)
- Life Sciences & Earth Sciences (AREA)
- Engineering & Computer Science (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Wood Science & Technology (AREA)
- Organic Chemistry (AREA)
- Emergency Medicine (AREA)
- Health & Medical Sciences (AREA)
- Detergent Compositions (AREA)
- Acyclic And Carbocyclic Compounds In Medicinal Compositions (AREA)
- Fodder In General (AREA)
- Separation Of Suspended Particles By Flocculating Agents (AREA)
Description
WO 97/45515 PCT/EP97/02161 1 IMPROVEMENTS RELATING TO LIMESCALE REMOVING COMPOSITIONS Technical Field The present invention relates to compositions for the removal of limescale and/or other mineral deposits from hard surfaces.
Background to the Invention Limescale mainly comprises calcium and magnesium carbonates, and can contain lesser amounts of soap scum, protein, particulates and other soils. Limescale is formed on evaporation of water containing said soils.
While the deposit formed by evaporation is initially paste-like, it hardens with time to form a recalcitrant deposit.
Conventional cleaning compositions are generally buffered at alkaline pH so as to attack fatty soils. Limescale is resistant to the action of alkali and specialist cleaning compositions, of acid pH, are used to remove it.
It is known that the use of strong acids, such as hydrochloric acid will result in prompt removal of limescale but will also result in damage to surrounding surfaces, such as bath enamels, metals and certain polymers, where these are susceptible to attack by strong acids.
Limescale removing compositions of maleic acid in combination with nonionic surfactants, either in further combination with ionic detergents or with phosphoric acid WO 97/45515 PCT/EP97/02161 2 are known. In the absence of nonionic surfactants cleaning efficiency is greatly reduced. Maleic acid is known to be a particularly effective limescale remover and is less prone to attack surfaces than the inorganic acids.
EP 0496188 relates to compositions with 1-15% nonionic and 4-25% of maleic acid, having a pH of 1-4.
Preferred compositions are formulated at pH 1-4 and comprise maleic and nonionic at specified levels but which are substantially free of both ionic detergents and phosphoric acid.
The use of other organic acids is known: GB-B-2149419 (Colgate-Palmolive: filed November 1983) relates to an acidic liquid cleaning composition of pH 3-5 which comprises a surfactant, water, a minor proportion of a non-sequestering acid which reacts with Ca and Mg soaps of higher fatty acids in soap scum (examples include glutaric acid) and a lesser minor proportion of an acid which forms a water insoluble calcium salt (phosphoric acid is given as an example), both acids being partially neutralised to a pH of EP-B-0411708 (Colgate-Palmolive: filed 31 July 1989) relates to an acidic (pH 1-4) aqueous cleaner for baths which are acid resistant or of zirconium white enamel which comprises surfactant, a C2-C10 organic acid other than oxalic and malonic acid, an aminoalkylenephosphonic acid and phosphoric acid.
EP-B-0040343 (BASF: filed 16 May 1980) is a granted European patent which relates to a composition comprising ethoxylated alcohol nonionic surfactant and C4-C8 aliphatic dicarboxylic acids or mixtures of such. The acids are present as 'colour stabilizers' and include a mixture of succinic, adipic and glutaric acids in the examples of the patent.
WO 97/45515 PCTIEP97/02161 -3 EP 0606712 (Clorox: published July 1994) relates to pH approx 2-3.5 cleaning formulations for the removal of mineral deposits which contain 3-10% in total of both a weak acid and its conjugate base at a molar ratio of 1:30 to 30:1 in which the weak acid has a pKa of 2-3.5. The compositions disclosed in this specification comprise citric acid (a tricarboxylic acid) and sodium citrate dihydrate as the limescale removing acids.
Despite the formulation work which had been done in this area it is believed that it is difficult to make formulations which are stable at low temperatures and/or which contain significant levels of succinic and adipic acids. This is especially true of concentrated systems which comprise around 8% of the dicarboxylic acid or acids when these compositions are shipped or stored at temperatures below 5 Celcius, where the precipitation of the acid is irreversible. Such temperatures may be encountered both during storage and shipping of a product prior to its commercial sale and while the product is being stored by the end user. While reversible precipitation may occur at lower acid levels this can still cause difficulties for the user who may not be aware that the precipitation has occurred (due to the opaque packaging which is used for these products) and may use the liquor above the precipitate without first warming the composition.
Brief Description of the Invention We have now determined that limescale-removing compositions of pH 1-5, comprising: a) a dicarboxylic acid, WO 97/45515 PCTIEP97/02161 4b) a fatty acid and c) an anionic surfactant other than fatty acid are stable at lower temperatures than similar compositions which do not contain the fatty acid. It is believed that the fatty acid acts as a solubiliser for the dicarboxylic acids but the details of the mechanism are not fully understood.
Accordingly a first aspect of the present invention provides a limescale-removing composition of pH comprising: a) 1-15%wt of a dicarboxylic acid, b) 0.1-10%wt of a fatty acid, and c) 1-30%wt of an anionic surfactant other than fatty acid A second aspect of the present invention provides for the use, as a low temperature stabilising additive in a limescale removing composition comprising 1-15%wt of a dicarboxylic acid and 1-30%wt of an anionic surfactant other than fatty acid, of 0.1-10%wt of a fatty acid.
Detailed Description of the Invention In the following description all quantities are given in wt% on product unless noted otherwise.
WO 97/45515 PCT/EP97/02161 Dicarboxylic Acids: Dicarboxylic acids suitable for use in the present invention include adipic, glutaric and succinic acid and mixtures thereof. The mixtures are preferred as these are commercially available. Typical mixtures which can be found in the marketplace comprise 30-35% adipic acid, glutaric acid and 10-18% succinic acid. Such a mixture is available in the marketplace as Sokalan DCS (TM, ex. BASF). Another suitable mixture is available as Radimix (TM, ex. Radici). The use of essentially pure acids is not excluded but these have limited commercial availability and the mixed acids are preferred.
Typical levels of total dicarboxylic acid in the product range from 2-10%wt. Levels of 3-5% are preferred for dilute compositions and levels of 6-9% for concentrates.
Fatty Acids: Fatty acids suitable for use in the compositions of the present invention include moncarboxylic acids with an average carbon chain length in the range C10-C18, preferably C12-C16.
C14 average chain length linear fatty acids (derivable from lauric acid oils such as coconut and palm-kernel fats) are particularly preferred. Longer chain length fatty acids are less soluble in the absence of expensive hydrotropes (such as alcohol and alkaryl sulphonates) or organic solvents. Suitable fatty acids are available in the marketplace as PRIFAC 7907 (TM ex. Unichema).
Typical levels of fatty acids range from 0.1-3%wt on product, with a range of 0.1-l%wt being particularly WO 97/45515 PCT/EP97/02161 6 preferred. Typical levels in dilute compositions are 0.25%wt with 0.5%wt being used in more concentrated products.
Surfactants: Preferably the anionic surfactant comprises one or more of the group comprising: primary and secondary alcohol sulphates, alcohol alkoxy sulphates, primary and secondary alkane sulphonates and alkyl aryl sulphonates.
The preferred anionic surfactants are the alcohol alkoxy sulphates, preferably the ether-sulphates. Most preferably average chain length ether sulphates with an average of 0.5-3 moles of ethoxylation. Lauryl ether sulphate (1EO) is a suitable anionic surfactant for compositions of the invention.
Preferred levels of anionic surfactant range from 2-14%wt.
Preferably 3-7%wt surfactant is present in dilute compositions and 8-12%wt is present in concentrated compositions.
Corrosion Inhibitors: Typically the compositions of the invention comprise one or more corrosion inhibitors. Phosphoric acid is a suitable corrosion inhibitor, and when present is conveniently employed at a level of 0.1-5%wt with levels of 0.5%wt being used in ditute product and l%wt being used in concentrated products.
WO 97/45515 PCT/EP97/02161 7
PH:
It is believed important that the pH of the composition is below the pKa of the fatty acid being employed. In general, the pKa of a C12-C16 fatty acid will be close to 4.9, consequently the pH of the compositions will generally be below this figure. Given that damage to surfaces can occur at pH's below 3.0 it is particularly preferred that the pH of the compositions of the invention falls into the range 3.0-4.5, with a pH of around being typical. Sodium hydroxide or another suitable base is used to regulate the pH if required. Typical levels of base in the products of the invention are 0.1-l%wt.
Minors: Preferred levels of perfume range from 0.1-2%wt. Acid stable perfumes are available from a variety of sources including the Quest company.
Various minor components may be present in the compositions of the present invention, these include opacifiers, colours, preservatives and fluorescers.
Typically, the present invention provides a limescaleremoving compositions of pH 3.0-4.9, comprising: a) 2-10%wt of one or more dicarboxylic acids selected from adipic acid, succinic acid and glutaric acid, b) 0.1-3.0%wt of an (on average) fatty acid, c) 2-14%wt of CI,-C, alcohol alkoxy sulphate with an average of 0.5-3 moles of ethoxylation, WO 97/45515 PCT/EP97/02161 8 d) 0-5% phosphoric acid, e) 0-5% base Preferred formulations for direct use comprise: a) 3-5%wt of a mixture of adipic acid, succinic acid and glutaric acid, b) 0.1-0.5%wt of an (on average) fatty acid, c) 3-7%wt of CI 0 -Ci, ether sulphate (0.5-3 EO) d) 0.1-5% phosphoric acid, e) 0-5% base Preferred concentrated formulations: a) 6-9%wt of a mixture of adipic acid, succinic acid and glutaric acid, b) 0.3-1.0%wt of an (on average) C fatty acid, c) 8-13%wt of ether sulphate (0.5-3 EO), d) 0.1-5% phosphoric acid, e) 0-5% base The present invention will be further described with reference to the following non-limiting examples.
WO 97/45515 PCT/EP97/02161 9 Examples Materials used in the examples are identified as follows: LES 1EO Fatty Acid Dicarb Acid Phos. Acid Base Preservative Perfume Lauryl ether sulphate with one mole of ethoxylation PRIFAC 7907 (TM) ex. Unichema Radimix (TM) ex. Radici or Sokalan DCS (TM) ex. BASF or Succinic acid Phosphoric Acid Sodium Hydroxide PROXEL GXL(TM, ex ICI) (1,2benzisothiazolin-3-one) GC 1550 A ex Quest Compositions were prepared by mixing of the components.
Compositions were prepared with proportions as given in Table 1 below, all components being given in wt% as 100%wt.
TABLE 1 Example 1 2 LES 1EO 5.0 10.0 Fatty Acid 0.25 Dicarb Acid 4.0 Phos. Acid 0.5 Base 0.38 0.76 Preservative 0.016 0.032 Perfume 0.5 Water to 100 to 100 WO 97/45515 PCT/EP97/02161 10 Experiments were also performed with each of the dicarboxylic acids mentioned above in the absence of the fatty acid. It was determined that after storage at temperatures below 5 0 C irreversible precipitation of the mixed dicarboxylic acids as crystals occurred when these were present at a concentration of In the diluted composition mixed acids) the precipitation is reversible. Similar results were obtained with succinic acid alone: in this case, we have problems of irreversible precipitation were encountered at 0°C even with the diluted version succinic acid).
For the compositions given in table 1 above no solubility problem was detected with both Sokalan DCS and Radimix and also with Succinic acid alone: while the product became slightly turbid at low temperatures precipitation of dicarboxylic acid crystals did not occur.
Claims (4)
1. A limescale-removing composition of pH 1-5, comprising: a) 1-15%wt of a dicarboxylic acid, b) 0.1-10%wt of a fatty acid with an average carbon chain lenght of C10-C16, and c) 1-30%wt of an anionic surfactant other than fatty acid and which is free of organic solvents.
2. Composition according to claim 1 wherein the dicarboxylic acid comprises one or more of adipic, glutaric, succinic acid and mixtures thereof.
3. Composition according to claim 1 or 2 wherein the anionic surfactant comprises one or more of the group comprising: primary and secondary alcohol sulphates, alcohol alkoxy sulphates, primary and secondary alkane sulphonates and alkyl aryl sulphonates. Pgw)SAE C'219-anended claims 18.5.98 -12
4. A 1limescale- removing composition of pH 3.0-4.9, comprising: a) 2-lO%wt of one or more dicarboxylic acids selected from adipic acid, succinic acid and glutaric acid, 0.l-3.O%wt of an (on average) C 10 -C 16 fatty acid, 2-14%wt of CIO-CIO alcohol alkoxy sulphate with an average of 0.5-3 moles of ethoxylation,. d) 0-5% phosphoric acid, e) base and which is free of organic solvents. DATED_-_ b Sur\' e_ c on behalf of UNILEVER PLC yer Australia Limited
Applications Claiming Priority (3)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| GBGB9610965.7A GB9610965D0 (en) | 1996-05-24 | 1996-05-24 | Improvements relating to limescale removing compositions |
| GB9610965 | 1996-05-24 | ||
| PCT/EP1997/002161 WO1997045515A1 (en) | 1996-05-24 | 1997-04-25 | Improvements relating to limescale removing compositions |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| AU2772597A AU2772597A (en) | 1998-01-05 |
| AU723832B2 true AU723832B2 (en) | 2000-09-07 |
Family
ID=10794296
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| AU27725/97A Ceased AU723832B2 (en) | 1996-05-24 | 1997-04-25 | Improvements relating to limescale removing compositions |
Country Status (10)
| Country | Link |
|---|---|
| EP (1) | EP0912676B1 (en) |
| AR (1) | AR007213A1 (en) |
| AU (1) | AU723832B2 (en) |
| BR (1) | BR9709268A (en) |
| CA (1) | CA2254844C (en) |
| DE (1) | DE69710728T2 (en) |
| ES (1) | ES2171935T3 (en) |
| GB (1) | GB9610965D0 (en) |
| WO (1) | WO1997045515A1 (en) |
| ZA (1) | ZA973931B (en) |
Families Citing this family (3)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| FR2838130B1 (en) * | 2002-04-08 | 2004-05-28 | Rhodia Polyamide Intermediates | SOLID ANTI-SCALE FORMULATION BASED ON ADIPIC ACID AND ITS USE IN AUTOMATIC DISHWASHING |
| US10683468B1 (en) | 2017-06-05 | 2020-06-16 | Miguel Angel Regalado, Sr. | Water mineral cleaning solutions and related methods |
| US10988712B1 (en) | 2017-06-05 | 2021-04-27 | Miguel Angel Regalado, Sr. | Water mineral cleaning solutions and related methods |
Citations (3)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| EP0151517A2 (en) * | 1984-01-17 | 1985-08-14 | Unilever N.V. | Liquid detergent composition |
| WO1994009108A1 (en) * | 1992-10-16 | 1994-04-28 | Unilever Plc | Improvements in general purpose cleaning compositions |
| WO1995014756A1 (en) * | 1993-11-24 | 1995-06-01 | Unilever Plc | Limescale removing composition |
Family Cites Families (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JPS61157593A (en) * | 1984-12-28 | 1986-07-17 | ライオン株式会社 | Detergent composition for bathroom |
-
1996
- 1996-05-24 GB GBGB9610965.7A patent/GB9610965D0/en active Pending
-
1997
- 1997-04-25 BR BR9709268A patent/BR9709268A/en not_active IP Right Cessation
- 1997-04-25 DE DE69710728T patent/DE69710728T2/en not_active Expired - Lifetime
- 1997-04-25 AU AU27725/97A patent/AU723832B2/en not_active Ceased
- 1997-04-25 ES ES97921788T patent/ES2171935T3/en not_active Expired - Lifetime
- 1997-04-25 WO PCT/EP1997/002161 patent/WO1997045515A1/en not_active Ceased
- 1997-04-25 EP EP97921788A patent/EP0912676B1/en not_active Expired - Lifetime
- 1997-04-25 CA CA002254844A patent/CA2254844C/en not_active Expired - Fee Related
- 1997-05-07 ZA ZA973931A patent/ZA973931B/en unknown
- 1997-05-21 AR ARP970102142A patent/AR007213A1/en unknown
Patent Citations (3)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| EP0151517A2 (en) * | 1984-01-17 | 1985-08-14 | Unilever N.V. | Liquid detergent composition |
| WO1994009108A1 (en) * | 1992-10-16 | 1994-04-28 | Unilever Plc | Improvements in general purpose cleaning compositions |
| WO1995014756A1 (en) * | 1993-11-24 | 1995-06-01 | Unilever Plc | Limescale removing composition |
Also Published As
| Publication number | Publication date |
|---|---|
| WO1997045515A1 (en) | 1997-12-04 |
| GB9610965D0 (en) | 1996-07-31 |
| ES2171935T3 (en) | 2002-09-16 |
| EP0912676A1 (en) | 1999-05-06 |
| AU2772597A (en) | 1998-01-05 |
| BR9709268A (en) | 1999-08-10 |
| CA2254844A1 (en) | 1997-12-04 |
| CA2254844C (en) | 2003-10-21 |
| DE69710728D1 (en) | 2002-04-04 |
| EP0912676B1 (en) | 2002-02-27 |
| AR007213A1 (en) | 1999-10-13 |
| ZA973931B (en) | 1998-11-09 |
| DE69710728T2 (en) | 2004-07-08 |
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| Date | Code | Title | Description |
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| FGA | Letters patent sealed or granted (standard patent) |