WO2006072780A1 - Cleaning formulation - Google Patents
Cleaning formulation Download PDFInfo
- Publication number
- WO2006072780A1 WO2006072780A1 PCT/GB2006/000015 GB2006000015W WO2006072780A1 WO 2006072780 A1 WO2006072780 A1 WO 2006072780A1 GB 2006000015 W GB2006000015 W GB 2006000015W WO 2006072780 A1 WO2006072780 A1 WO 2006072780A1
- Authority
- WO
- WIPO (PCT)
- Prior art keywords
- formulation
- aluminium
- acid
- cleaning
- ions
- Prior art date
Links
- 239000000203 mixture Substances 0.000 title claims abstract description 78
- 238000009472 formulation Methods 0.000 title claims abstract description 77
- 238000004140 cleaning Methods 0.000 title claims abstract description 45
- 239000004411 aluminium Substances 0.000 claims abstract description 31
- 229910052782 aluminium Inorganic materials 0.000 claims abstract description 31
- XAGFODPZIPBFFR-UHFFFAOYSA-N aluminium Chemical compound [Al] XAGFODPZIPBFFR-UHFFFAOYSA-N 0.000 claims abstract description 31
- -1 hydroxyl ammonium ions Chemical class 0.000 claims abstract description 20
- 239000004094 surface-active agent Substances 0.000 claims abstract description 20
- 239000003352 sequestering agent Substances 0.000 claims abstract description 15
- OAKJQQAXSVQMHS-UHFFFAOYSA-N hydrazine Substances NN OAKJQQAXSVQMHS-UHFFFAOYSA-N 0.000 claims abstract description 14
- QAOWNCQODCNURD-UHFFFAOYSA-N Sulfuric acid Chemical compound OS(O)(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-N 0.000 claims abstract description 10
- 239000001117 sulphuric acid Substances 0.000 claims abstract description 9
- 235000011149 sulphuric acid Nutrition 0.000 claims abstract description 9
- 150000002500 ions Chemical class 0.000 claims abstract description 4
- 229910052723 transition metal Inorganic materials 0.000 claims abstract description 3
- 150000003624 transition metals Chemical class 0.000 claims abstract description 3
- 239000002253 acid Substances 0.000 claims description 17
- 239000012141 concentrate Substances 0.000 claims description 17
- KRKNYBCHXYNGOX-UHFFFAOYSA-N citric acid Chemical compound OC(=O)CC(O)(C(O)=O)CC(O)=O KRKNYBCHXYNGOX-UHFFFAOYSA-N 0.000 claims description 15
- VTLYFUHAOXGGBS-UHFFFAOYSA-N Fe3+ Chemical compound [Fe+3] VTLYFUHAOXGGBS-UHFFFAOYSA-N 0.000 claims description 11
- 229910001447 ferric ion Inorganic materials 0.000 claims description 11
- RBLWMQWAHONKNC-UHFFFAOYSA-N hydroxyazanium Chemical compound O[NH3+] RBLWMQWAHONKNC-UHFFFAOYSA-N 0.000 claims description 10
- 238000000034 method Methods 0.000 claims description 10
- IAYPIBMASNFSPL-UHFFFAOYSA-N Ethylene oxide Chemical compound C1CO1 IAYPIBMASNFSPL-UHFFFAOYSA-N 0.000 claims description 9
- 150000001735 carboxylic acids Chemical class 0.000 claims description 9
- KDYFGRWQOYBRFD-UHFFFAOYSA-N succinic acid Chemical compound OC(=O)CCC(O)=O KDYFGRWQOYBRFD-UHFFFAOYSA-N 0.000 claims description 9
- 150000002191 fatty alcohols Chemical class 0.000 claims description 8
- WNLRTRBMVRJNCN-UHFFFAOYSA-N adipic acid Chemical compound OC(=O)CCCCC(O)=O WNLRTRBMVRJNCN-UHFFFAOYSA-N 0.000 claims description 6
- 125000000217 alkyl group Chemical group 0.000 claims description 6
- 125000002887 hydroxy group Chemical group [H]O* 0.000 claims description 6
- 229910001428 transition metal ion Inorganic materials 0.000 claims description 6
- 239000001384 succinic acid Substances 0.000 claims description 5
- 125000004432 carbon atom Chemical group C* 0.000 claims description 4
- 239000001361 adipic acid Substances 0.000 claims description 3
- 235000011037 adipic acid Nutrition 0.000 claims description 3
- 150000007519 polyprotic acids Polymers 0.000 claims description 3
- 125000003158 alcohol group Chemical group 0.000 claims description 2
- 238000010790 dilution Methods 0.000 claims description 2
- 239000012895 dilution Substances 0.000 claims description 2
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 claims 2
- MHAJPDPJQMAIIY-UHFFFAOYSA-N Hydrogen peroxide Chemical compound OO MHAJPDPJQMAIIY-UHFFFAOYSA-N 0.000 description 10
- PNEYBMLMFCGWSK-UHFFFAOYSA-N Alumina Chemical compound [O-2].[O-2].[O-2].[Al+3].[Al+3] PNEYBMLMFCGWSK-UHFFFAOYSA-N 0.000 description 9
- 238000000576 coating method Methods 0.000 description 6
- 238000010409 ironing Methods 0.000 description 6
- 150000002978 peroxides Chemical class 0.000 description 6
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 6
- 239000011248 coating agent Substances 0.000 description 5
- 238000010186 staining Methods 0.000 description 5
- OFOBLEOULBTSOW-UHFFFAOYSA-N Malonic acid Chemical compound OC(=O)CC(O)=O OFOBLEOULBTSOW-UHFFFAOYSA-N 0.000 description 4
- 235000013361 beverage Nutrition 0.000 description 4
- 229910000838 Al alloy Inorganic materials 0.000 description 3
- XEEYBQQBJWHFJM-UHFFFAOYSA-N Iron Chemical class [Fe] XEEYBQQBJWHFJM-UHFFFAOYSA-N 0.000 description 3
- 229910002651 NO3 Inorganic materials 0.000 description 3
- NHNBFGGVMKEFGY-UHFFFAOYSA-N Nitrate Chemical compound [O-][N+]([O-])=O NHNBFGGVMKEFGY-UHFFFAOYSA-N 0.000 description 3
- 238000007739 conversion coating Methods 0.000 description 3
- 230000000694 effects Effects 0.000 description 3
- 238000011065 in-situ storage Methods 0.000 description 3
- 150000003839 salts Chemical class 0.000 description 3
- 239000000243 solution Substances 0.000 description 3
- KRHYYFGTRYWZRS-UHFFFAOYSA-N Fluorane Chemical compound F KRHYYFGTRYWZRS-UHFFFAOYSA-N 0.000 description 2
- AVXURJPOCDRRFD-UHFFFAOYSA-N Hydroxylamine Chemical class ON AVXURJPOCDRRFD-UHFFFAOYSA-N 0.000 description 2
- PXHVJJICTQNCMI-UHFFFAOYSA-N Nickel Chemical compound [Ni] PXHVJJICTQNCMI-UHFFFAOYSA-N 0.000 description 2
- NBIIXXVUZAFLBC-UHFFFAOYSA-N Phosphoric acid Chemical compound OP(O)(O)=O NBIIXXVUZAFLBC-UHFFFAOYSA-N 0.000 description 2
- QAOWNCQODCNURD-UHFFFAOYSA-L Sulfate Chemical compound [O-]S([O-])(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-L 0.000 description 2
- 150000007513 acids Chemical class 0.000 description 2
- 238000007792 addition Methods 0.000 description 2
- 125000000129 anionic group Chemical group 0.000 description 2
- BVKZGUZCCUSVTD-UHFFFAOYSA-N carbonic acid Chemical compound OC(O)=O BVKZGUZCCUSVTD-UHFFFAOYSA-N 0.000 description 2
- 238000006243 chemical reaction Methods 0.000 description 2
- 239000003795 chemical substances by application Substances 0.000 description 2
- 238000004519 manufacturing process Methods 0.000 description 2
- 238000002156 mixing Methods 0.000 description 2
- 239000007800 oxidant agent Substances 0.000 description 2
- 238000009928 pasteurization Methods 0.000 description 2
- BASFCYQUMIYNBI-UHFFFAOYSA-N platinum Chemical class [Pt] BASFCYQUMIYNBI-UHFFFAOYSA-N 0.000 description 2
- 229920001282 polysaccharide Polymers 0.000 description 2
- 239000005017 polysaccharide Substances 0.000 description 2
- 229910021653 sulphate ion Inorganic materials 0.000 description 2
- 238000005406 washing Methods 0.000 description 2
- HFVMEOPYDLEHBR-UHFFFAOYSA-N (2-fluorophenyl)-phenylmethanol Chemical compound C=1C=CC=C(F)C=1C(O)C1=CC=CC=C1 HFVMEOPYDLEHBR-UHFFFAOYSA-N 0.000 description 1
- UOFGSWVZMUXXIY-UHFFFAOYSA-N 1,5-Diphenyl-3-thiocarbazone Chemical compound C=1C=CC=CC=1N=NC(=S)NNC1=CC=CC=C1 UOFGSWVZMUXXIY-UHFFFAOYSA-N 0.000 description 1
- SQMOOVFBFVTTGF-UHFFFAOYSA-N 1-benzyl-1-phenylhydrazine Chemical compound C=1C=CC=CC=1N(N)CC1=CC=CC=C1 SQMOOVFBFVTTGF-UHFFFAOYSA-N 0.000 description 1
- XKLNOVWDVMWTOB-UHFFFAOYSA-N 2,3,4,9-tetrahydro-1h-carbazole Chemical compound N1C2=CC=CC=C2C2=C1CCCC2 XKLNOVWDVMWTOB-UHFFFAOYSA-N 0.000 description 1
- HORQAOAYAYGIBM-UHFFFAOYSA-N 2,4-dinitrophenylhydrazine Chemical compound NNC1=CC=C([N+]([O-])=O)C=C1[N+]([O-])=O HORQAOAYAYGIBM-UHFFFAOYSA-N 0.000 description 1
- KMVPXBDOWDXXEN-UHFFFAOYSA-N 4-nitrophenylhydrazine Chemical compound NNC1=CC=C([N+]([O-])=O)C=C1 KMVPXBDOWDXXEN-UHFFFAOYSA-N 0.000 description 1
- CPELXLSAUQHCOX-UHFFFAOYSA-M Bromide Chemical compound [Br-] CPELXLSAUQHCOX-UHFFFAOYSA-M 0.000 description 1
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical group [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 description 1
- VEXZGXHMUGYJMC-UHFFFAOYSA-M Chloride anion Chemical compound [Cl-] VEXZGXHMUGYJMC-UHFFFAOYSA-M 0.000 description 1
- CWYNVVGOOAEACU-UHFFFAOYSA-N Fe2+ Chemical class [Fe+2] CWYNVVGOOAEACU-UHFFFAOYSA-N 0.000 description 1
- KRHYYFGTRYWZRS-UHFFFAOYSA-M Fluoride anion Chemical compound [F-] KRHYYFGTRYWZRS-UHFFFAOYSA-M 0.000 description 1
- BGRDGMRNKXEXQD-UHFFFAOYSA-N Maleic hydrazide Chemical compound OC1=CC=C(O)N=N1 BGRDGMRNKXEXQD-UHFFFAOYSA-N 0.000 description 1
- ZOKXTWBITQBERF-UHFFFAOYSA-N Molybdenum Chemical compound [Mo] ZOKXTWBITQBERF-UHFFFAOYSA-N 0.000 description 1
- 229910017912 NH2OH Inorganic materials 0.000 description 1
- 229910019142 PO4 Inorganic materials 0.000 description 1
- BQCADISMDOOEFD-UHFFFAOYSA-N Silver Chemical class [Ag] BQCADISMDOOEFD-UHFFFAOYSA-N 0.000 description 1
- WNROFYMDJYEPJX-UHFFFAOYSA-K aluminium hydroxide Chemical compound [OH-].[OH-].[OH-].[Al+3] WNROFYMDJYEPJX-UHFFFAOYSA-K 0.000 description 1
- 229910021502 aluminium hydroxide Inorganic materials 0.000 description 1
- 229910000147 aluminium phosphate Inorganic materials 0.000 description 1
- REDXJYDRNCIFBQ-UHFFFAOYSA-N aluminium(3+) Chemical compound [Al+3] REDXJYDRNCIFBQ-UHFFFAOYSA-N 0.000 description 1
- RAESLDWEUUSRLO-UHFFFAOYSA-O aminoazanium;nitrate Chemical compound [NH3+]N.[O-][N+]([O-])=O RAESLDWEUUSRLO-UHFFFAOYSA-O 0.000 description 1
- 150000001450 anions Chemical class 0.000 description 1
- RJGDLRCDCYRQOQ-UHFFFAOYSA-N anthrone Chemical compound C1=CC=C2C(=O)C3=CC=CC=C3CC2=C1 RJGDLRCDCYRQOQ-UHFFFAOYSA-N 0.000 description 1
- 239000002585 base Substances 0.000 description 1
- 235000013405 beer Nutrition 0.000 description 1
- 229910021538 borax Inorganic materials 0.000 description 1
- 230000003197 catalytic effect Effects 0.000 description 1
- 125000002091 cationic group Chemical group 0.000 description 1
- 150000003841 chloride salts Chemical class 0.000 description 1
- 230000000052 comparative effect Effects 0.000 description 1
- 150000001875 compounds Chemical class 0.000 description 1
- 239000000356 contaminant Substances 0.000 description 1
- 239000013530 defoamer Substances 0.000 description 1
- JGUQDUKBUKFFRO-CIIODKQPSA-N dimethylglyoxime Chemical compound O/N=C(/C)\C(\C)=N\O JGUQDUKBUKFFRO-CIIODKQPSA-N 0.000 description 1
- 230000008030 elimination Effects 0.000 description 1
- 238000003379 elimination reaction Methods 0.000 description 1
- 230000007613 environmental effect Effects 0.000 description 1
- 238000005530 etching Methods 0.000 description 1
- 239000012458 free base Substances 0.000 description 1
- 150000004676 glycans Chemical class 0.000 description 1
- PCHJSUWPFVWCPO-UHFFFAOYSA-N gold Chemical class [Au] PCHJSUWPFVWCPO-UHFFFAOYSA-N 0.000 description 1
- 229910052737 gold Inorganic materials 0.000 description 1
- 239000010931 gold Chemical class 0.000 description 1
- 238000010438 heat treatment Methods 0.000 description 1
- ZGCHATBSUIJLRL-UHFFFAOYSA-N hydrazine sulfate Chemical compound NN.OS(O)(=O)=O ZGCHATBSUIJLRL-UHFFFAOYSA-N 0.000 description 1
- 150000001261 hydroxy acids Chemical class 0.000 description 1
- VGYYSIDKAKXZEE-UHFFFAOYSA-L hydroxylammonium sulfate Chemical compound O[NH3+].O[NH3+].[O-]S([O-])(=O)=O VGYYSIDKAKXZEE-UHFFFAOYSA-L 0.000 description 1
- 229910052742 iron Inorganic materials 0.000 description 1
- 229910000360 iron(III) sulfate Inorganic materials 0.000 description 1
- 239000000314 lubricant Substances 0.000 description 1
- 239000010687 lubricating oil Substances 0.000 description 1
- WPBNNNQJVZRUHP-UHFFFAOYSA-L manganese(2+);methyl n-[[2-(methoxycarbonylcarbamothioylamino)phenyl]carbamothioyl]carbamate;n-[2-(sulfidocarbothioylamino)ethyl]carbamodithioate Chemical class [Mn+2].[S-]C(=S)NCCNC([S-])=S.COC(=O)NC(=S)NC1=CC=CC=C1NC(=S)NC(=O)OC WPBNNNQJVZRUHP-UHFFFAOYSA-L 0.000 description 1
- 230000000873 masking effect Effects 0.000 description 1
- 239000002184 metal Substances 0.000 description 1
- 229910001092 metal group alloy Inorganic materials 0.000 description 1
- 229910052750 molybdenum Inorganic materials 0.000 description 1
- 239000011733 molybdenum Substances 0.000 description 1
- 238000000465 moulding Methods 0.000 description 1
- 229910052759 nickel Inorganic materials 0.000 description 1
- 125000000449 nitro group Chemical group [O-][N+](*)=O 0.000 description 1
- YUWVDIIHTJLPRI-UHFFFAOYSA-N phenylhydrazine;sulfuric acid Chemical compound OS(O)(=O)=O.NNC1=CC=CC=C1 YUWVDIIHTJLPRI-UHFFFAOYSA-N 0.000 description 1
- NBIIXXVUZAFLBC-UHFFFAOYSA-K phosphate Chemical compound [O-]P([O-])([O-])=O NBIIXXVUZAFLBC-UHFFFAOYSA-K 0.000 description 1
- 239000010452 phosphate Substances 0.000 description 1
- 229910052697 platinum Inorganic materials 0.000 description 1
- 229920001983 poloxamer Polymers 0.000 description 1
- 229910052709 silver Inorganic materials 0.000 description 1
- 239000004332 silver Chemical class 0.000 description 1
- 239000004328 sodium tetraborate Substances 0.000 description 1
- 235000010339 sodium tetraborate Nutrition 0.000 description 1
- 235000014214 soft drink Nutrition 0.000 description 1
- 238000005507 spraying Methods 0.000 description 1
- 238000009736 wetting 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
- C11D1/66—Non-ionic compounds
- C11D1/662—Carbohydrates or derivatives
-
- C—CHEMISTRY; METALLURGY
- C11—ANIMAL OR VEGETABLE OILS, FATS, FATTY SUBSTANCES OR WAXES; FATTY ACIDS THEREFROM; DETERGENTS; CANDLES
- C11D—DETERGENT COMPOSITIONS; USE OF SINGLE SUBSTANCES AS DETERGENTS; SOAP OR SOAP-MAKING; RESIN SOAPS; RECOVERY OF GLYCEROL
- C11D1/00—Detergent compositions based essentially on surface-active compounds; Use of these compounds as a detergent
- C11D1/66—Non-ionic compounds
- C11D1/72—Ethers of polyoxyalkylene glycols
-
- 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
- C11D3/00—Other compounding ingredients of detergent compositions covered in group C11D1/00
- C11D3/02—Inorganic compounds ; Elemental compounds
- C11D3/04—Water-soluble compounds
- C11D3/044—Hydroxides or bases
-
- 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
- C11D3/20—Organic compounds containing oxygen
- C11D3/2075—Carboxylic acids-salts thereof
- C11D3/2086—Hydroxy carboxylic acids-salts thereof
-
- C—CHEMISTRY; METALLURGY
- C23—COATING METALLIC MATERIAL; COATING MATERIAL WITH METALLIC MATERIAL; CHEMICAL SURFACE TREATMENT; DIFFUSION TREATMENT OF METALLIC MATERIAL; COATING BY VACUUM EVAPORATION, BY SPUTTERING, BY ION IMPLANTATION OR BY CHEMICAL VAPOUR DEPOSITION, IN GENERAL; INHIBITING CORROSION OF METALLIC MATERIAL OR INCRUSTATION IN GENERAL
- C23G—CLEANING OR DE-GREASING OF METALLIC MATERIAL BY CHEMICAL METHODS OTHER THAN ELECTROLYSIS
- C23G1/00—Cleaning or pickling metallic material with solutions or molten salts
- C23G1/02—Cleaning or pickling metallic material with solutions or molten salts with acid solutions
- C23G1/12—Light metals
- C23G1/125—Light metals aluminium
-
- 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
- C11D2111/00—Cleaning compositions characterised by the objects to be cleaned; Cleaning compositions characterised by non-standard cleaning or washing processes
- C11D2111/10—Objects to be cleaned
- C11D2111/14—Hard surfaces
- C11D2111/16—Metals
Definitions
- the present invention relates to a cleaning formulation, to its use in cleaning a surface comprised of aluminium or an aluminium alloy, and to a concentrate for preparing the formulation.
- the invention relates particularly, but by no means " exclusively, to such a formulation and method for use in the production of an aluminium or aluminium alloy container (e.g. a can) for holding a beverage such as beer or a soft drink.
- This invention may or may not be used to prepare such a container for either a pasteurisation or retortable process.
- aluminium as used in the remainder of this specification is intended to cover both aluminium metal and aluminium alloys.
- Aluminium cans for holding beverages are produced by a process in which an opened-top cylindrical can body (including an integral base) is formed by a moulding operation known in the art as drawing and ironing. (The upper end cap is formed separately and applied to construct the "closed” can at a separate stage in the process). The surface of the can body is then protected by application of a coating thereto, e.g. of the type known as a "conversion coating".
- US-A-4 980 076 proposes a fluoride- free etchant rinse for aluminium containing a phosphoric acid component, a further acid component (e.g. sulphuric acid), ferric ions, an oxidising agent (such as hydrogen peroxide) to maintain a required concentration of ferric ions, an aluminium ion sequestrant (e.g. a polybasic and/or hydroxy acid) and at least one surface active agent.
- a fluoride- free etchant rinse for aluminium containing a phosphoric acid component, a further acid component (e.g. sulphuric acid), ferric ions, an oxidising agent (such as hydrogen peroxide) to maintain a required concentration of ferric ions, an aluminium ion sequestrant (e.g. a polybasic and/or hydroxy acid) and at least one surface active agent.
- a fluoride- free etchant rinse for aluminium containing a phosphoric acid component, a further
- PCT-GB2004/002729 discloses a cleaning formulation intended particularly for use in cleaning aluminium can bodies which comprises a carboxylic acid (e.g. a di-basic acid), a peroxide (e.g. hydrogen peroxide), ferric ions, surface active agents and a polysaccharide compound (such as a polyglucoside) which is preferably alkylated, ethoxylated or propoxylated.
- a carboxylic acid e.g. a di-basic acid
- a peroxide e.g. hydrogen peroxide
- ferric ions e.g. hydrogen peroxide
- surface active agents e.g. hydrogen peroxide
- a polysaccharide compound such as a polyglucoside
- the above described cleaning formulation may be produced from concentrates which are diluted to end-use concentration for the purpose of the cleaning operation.
- a cleaning formulation for cleaning aluminium surfaces having a pH of 0.5 to 5 and incorporating sulphuric acid at least one aluminium sequestrant, at least one surface active agent and ions of at least one d-block transition metal characterised in that the formulation also incorporates substituted or unsubstituted hydroxyl ammonium ions or hydrazine ions.
- the invention has been based on our finding that the use of substituted or unsubstituted hydroxyl ammonium or hydrazine ions provides significantly improved results in the cleaning of aluminium as compared to similar formulations which incorporate peroxide as an oxidising agent. More particularly, the use of such ions provides significantly improved removal of aluminium oxide from the surface of the aluminium.
- cleaning formulations in accordance with the invention are particularly useful for the cleaning of aluminium can bodies produced by a drawing and ironing operation to effect removable thereof so that a good quality conversion coat may subsequently be applied. Such coated cans are not prone to dome-staining when subjected to a pasteurising operation.
- each component of the formulation is preferably present in the amount indicated in the following table, with more preferred amounts for each component being given in the following description:
- the amount of the substituted or unsubstituted hydroxyl ammonium or hydrazine ions present in the formulation is preferably in the range 0.0004 to 0.05%, more preferably 0.0004 to 0.02% and even more preferably 0.004 to 0.008% by weight of the formulation.
- the substituted or unsubstituted hydroxyl ammonium or hydrazine ions may be introduced into the cleaning formulation in the form of salts or in the form of the corresponding free base, which is converted in situ in the acid conditions prevailing in the bath to the corresponding substituted or unsubstituted hydroxyl ammonium or hydrazine ions.
- the hydroxyl ammonium or hydrazine ions may be of the formula H 3 XN + where X is -OH, -NH 2 or -NH 3 + .
- X is -OH, i.e. H 3 XN + represents the hydroxyl ammonium ion.
- the formulation may, for example, be prepared from a hydroxyl ammonium salt which can incorporate a wide variety of anions, e.g. sulphate, phosphate, chloride, nitrate or bromide. It is however also possible to prepare the formulation from NH 2 OH which (as indicated above) is converted in situ in the acid conditions of the formulation to the hydroxyl ammonium ion.
- the formulation is prepared from hydroxyl ammonium sulphate.
- Substituted or unsubstituted hydrazine ions may be provided by sulphate, nitrate, nitro or chloride salts.
- Particular examples include phenyl hydrazine sulphate, p-nitro phenyl hydrazine, benzyl phenyl hydrazine, maleic hydrazine, hydrazine sulphate, hydrazine di-mono hydrochloride, 2,4-dinitrophenyl hydrazine, anthrone, dithizone, 1,2,3,4-tetrahydrocarbazole, dimethylglyoxime, and hydrazine nitrate.
- the d-block transition metal ion is preferably present in the formulation in an amount 0.0001-0.015%, more preferably 0.003-0.006%.
- the d-block transition metal ion may for example be provided by salts of iron, platinum, silver, gold, manganese, nickel or molybdenum.
- the d-block transition metal ion is preferably the ferric ion (Fe 3+ ).
- the ferric ion is provided by a ferric salt such as Fe 2 (SO 4 ) 3 , Fe(NO 3 ) 2 orFe 2 (CO 4 ) 3 .
- ferric ions may be produced in situ from ferrous salts which are converted under the oxidising conditions of the cleaning formulation to provide the ferric ions.
- the amount of aluminium sequestrant present in the formulation is preferably 0.005-0.25% by weight, more preferably 0.05-0.1%.
- the aluminium sequestrant is preferably provided by at least one carboxylic acid.
- the carboxylic may be provided at least partly by a di- or higher- basic carboxylic acid.
- the acid may, for example, be of the formula HOOC (CEb) n COOH with n preferably being from 0 to 4 so that the acid has a maximum of 6 carbon atoms, this being preferred to ensure that the di-basic acid (of the indicated formula) is water-soluble. It is however also possible to use di-basic acids that also incorporate at least one hydroxyl group to improve water solubility, in which case the acid may contain more than 6 carbon atoms.
- the di-basic acid may be malonic acid, succinic acid or adipic acid.
- malonic or succinic acid are used.
- the sequestrant comprises a mixture of a di-basic acid of the formula HOOC(CH 2 ) n COOH (where n is as defined above) and a carboxylic acid (preferably a poly-basic carboxylic acid) containing a hydroxyl group.
- This latter acid may be a di- or higher- basic carboxylic acid (also containing a hydroxyl group) and is most preferably citric acid.
- the improved results obtained by the combination of these two acids reside in an improvement in the brightness of the interior of the can body after conversion coating.
- the amount of acid of the formula HOOC(CH 2 ) n COOH in the formulation is in the range 0.02-0.06% as also is the amount of the hydroxycarboxylic acid (e.g. citric acid). It is particularly preferred that the amount of acid of the formula HOOC(CH 2 ) n COOH is in the range 0.02-0.04% whereas the amount of the hydroxycarboxylic acid is in the range 0.03-0.06%.
- the cleaning formulation contains a total amount of 0.004-0.25% (more preferably 0.04-0.1%) of surface active agents.
- the surface active agents may be cationic, anionic, non-anionic or amphoteric agents, suitable examples of which are disclosed in US-A-4 980 076 (Nihon Parkerizing). It is however particularly preferred that the surface active agents are non-ionic agents.
- the surface active agent comprises at least one fatty alcohol ethoxylate.
- the or each such surfacactant may have an alcohol residue containing 8- 15 carbon atoms and may incorporate 4-15 moles of ethylene oxide (per mole of fatty alcohol residue).
- the surface active agent system comprises 0.01-0.04% by weight (based on the total weight of the cleaning formulation) of each of:
- a fatty alcohol (C 13 ) ethoxylate with 8 moles of ethylene oxide e.g. as available under the names Caflon TD0900 or Lutensol T08;
- a fatty alcohol (C 10 ) ethoxylate with 4 moles of ethylene oxide e.g. as available under the names Rhodaclean MSC or Lutensol XL40.
- the surface active agent system preferably also includes a surface active agent incorporating polysaccharide (e.g. polyglucoside) residues.
- a surface active agent e.g. polyglucoside
- Such a surface active agent is preferably present in an amount 0.005-0.02% by weight of the formulation.
- Suitable surface active agents in this category are alkylated, ethoxylated or propoxylated polyglucosides. Alkyl polyglucosides are particularly preferred, in particular those in which the alkyl residue has a carbon chain length of C 12 -C 16 .
- the formulation may incorporate a defoamer, e.g. Pluronic PE6100.
- the cleaning formulation further incorporates sulphuric acid, preferably in an amount of 0.05 to 1%, more preferably 0.1% to 0.5%, by weight (expressed as H 2 SO 4 ) of the formulation.
- the cleaning formulation of the invention has a pH of 0.5 to 5, more preferably 0.5 to 3.0, even more preferably 0.5 to 2.5.
- the cleaning operation may be carried out by immersing the can bodies in the cleaning formulation or alternatively by spraying the bodies with the formulation.
- the cleaning formulation will be at a temperature of 20-80°C, more preferably 50-70°C.
- the cleaning operation will be effected for a period of 10 to 120 seconds.
- the aluminium After being treated with the cleaning formulation, the aluminium may be washed with water.
- a cleaning formulation in accordance with the invention may be prepared by admixing the individual components in the required amounts in water. Conveniently however a cleaning formulation in accordance with the invention is obtained by dilution of a pre-prepared concentrate.
- a typical concentrate formulation is as shown below:
- the above concentrate may be prepared without the sulphuric acid, in which case the concentrate and sulphuric acid are added separately to water to produce the final cleaning formulation. If the concentrate contains sulphuric acid then the amount is preferably in the range 15% to 25% by weight of the concentrate.
- the aluminium sequestrant preferably comprises 1-5% by weight of a di-basic carboxylic acid of the formula HOOC(CH 2 ) n COOH, where n is 0 to 4 and 1-5% of a poly-basic acid containing a hydroxyl group.
- the sequestrant preferably comprises succinic or adipic acid and citric acid.
- the surface active agent preferably comprises 0.5 to 2.5% by weight of each of:
- a fatty alcohol (C 13 ) ethoxylate with 8 moles of ethylene oxide e.g. as available under the names Caflon TD0900 or Lutensol T08;
- a fatty alcohol (C 1O ) ethoxylate with 4 moles of ethylene oxide e.g. as available under the names Rhodaclean MSC or Lutensol XL40.
- a concentrate was prepared from the following components:
- the concentrate was prepared by heating the water to 25 0 C and adding the succinic acid with thorough mixing. The remaining components were then added in the order listed with thorough mixing between additions and for one hour after addition of the final component.
- the diluted concentrate was used for cleaning aluminium can bodies that had been produced by a standard drawing and ironing operation. Cleaning was effected by washing the cans (using the wash solution detailed above) in a household dishwasher for 3 minutes at 55°C to 60°C (low pressure). Sufficient amount of the concentrate was added to produce an approximately 1% solution of the cleaning formulation.
- the cleaned cans were then subjected to a washing operation with water.
- One can was then subjected to a "dome staining" test in which the can was immersed in a solution of borax (0.3 g I "1 ) at 80 0 C for 20 minutes.
- a further (cleaned) can was given a "conversion coat" using Houghto-Coat NC900 at a pH 2.9 for 40 seconds at 40 0 C.
- the coated can was then subjected to the "dome-staining" test described above.
- Example 2 The procedure of Example 1 was repeated but using a peroxide-based cleaning formulation of the type described in PCT/GB 2004/002729 (Natech Ltd). The results are shown in Fig 2 in which the coated can is on the right hand side.
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Life Sciences & Earth Sciences (AREA)
- Engineering & Computer Science (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Oil, Petroleum & Natural Gas (AREA)
- Wood Science & Technology (AREA)
- Health & Medical Sciences (AREA)
- Inorganic Chemistry (AREA)
- Emergency Medicine (AREA)
- Molecular Biology (AREA)
- General Chemical & Material Sciences (AREA)
- Materials Engineering (AREA)
- Mechanical Engineering (AREA)
- Metallurgy (AREA)
- Detergent Compositions (AREA)
Abstract
A cleaning formulation for cleaning aluminium surfaces. The formulation has a pH of 0.5 to 5 and incorporates sulphuric acid, at least one aluminium sequestrant, at least one surface active agent, ions of at least one d-block transition metal, and substituted or unsubstituted hydroxyl ammonium ions or hydrazine ions.
Description
CLEANING FORMULATION
The present invention relates to a cleaning formulation, to its use in cleaning a surface comprised of aluminium or an aluminium alloy, and to a concentrate for preparing the formulation. The invention relates particularly, but by no means "exclusively, to such a formulation and method for use in the production of an aluminium or aluminium alloy container (e.g. a can) for holding a beverage such as beer or a soft drink. This invention may or may not be used to prepare such a container for either a pasteurisation or retortable process.
For convenience, the term "aluminium" as used in the remainder of this specification is intended to cover both aluminium metal and aluminium alloys.
Aluminium cans for holding beverages are produced by a process in which an opened-top cylindrical can body (including an integral base) is formed by a moulding operation known in the art as drawing and ironing. (The upper end cap is formed separately and applied to construct the "closed" can at a separate stage in the process). The surface of the can body is then protected by application of a coating thereto, e.g. of the type known as a "conversion coating".
It is however generally not possible simply to apply the coating to the can body immediately after it has been formed in the drawing and ironing operation. This is because the operation involves the use of lubricants that must be removed from the can body before a satisfactory coating can then be applied. Additionally the can body resulting from the drawing and ironing operation would include surface aluminium oxide which must likewise be removed before a satisfactory coating can be applied.
Consequently the can bodies must be cleaned to remove lubricating oils and surface oxides before they are passed to the coating process.
Many prior art formulations for cleaning aluminium (e.g. in the production of beverage cans) incorporate fluoride ions (e.g. in the form of hydrofluoric acid).
However such formulations have disadvantages from the safety and environmental point of view. As a result, various "fluoride-free" formulations have been proposed. Generally such formulations have a pH of 0.5 to 3 and incorporate ferric ions and hydrogen peroxide.
Thus, for example, US-A-4 980 076 (Nihon Parkerizing) proposes a fluoride- free etchant rinse for aluminium containing a phosphoric acid component, a further acid component (e.g. sulphuric acid), ferric ions, an oxidising agent (such as hydrogen peroxide) to maintain a required concentration of ferric ions, an aluminium ion sequestrant (e.g. a polybasic and/or hydroxy acid) and at least one surface active agent.
PCT-GB2004/002729 (Natech Ltd) discloses a cleaning formulation intended particularly for use in cleaning aluminium can bodies which comprises a carboxylic acid (e.g. a di-basic acid), a peroxide (e.g. hydrogen peroxide), ferric ions, surface active agents and a polysaccharide compound (such as a polyglucoside) which is preferably alkylated, ethoxylated or propoxylated.
The above described cleaning formulation may be produced from concentrates which are diluted to end-use concentration for the purpose of the cleaning operation.
We have however found that the cleaning of aluminium can bodies (produced by a drawing and ironing operation) using formulations containing ferric ions and a peroxide (such as hydrogen peroxide) does not achieve sufficient removal of aluminium oxide to provide a good coating. In particular, pasteurisation of the filled cans gives "dome staining" on the (externally visible) concave under-surface of the can. Such "dome staining" is regarded as aesthetically undesirable and may lead (potential) purchasers of the cans to believe that the beverage therein has somehow deteriorated, although this is not the case. We believe that this disadvantage is caused by the fact that the peroxide is unstable under the acid conditions and breaks down so that a satisfactory cleaning process is not achieved.
It is an object of the present invention to obviate or mitigate the above- mentioned disadvantages.
According to a first aspect of the present invention there is provided a cleaning formulation for cleaning aluminium surfaces, the formulation having a pH of 0.5 to 5 and incorporating sulphuric acid at least one aluminium sequestrant, at least one surface active agent and ions of at least one d-block transition metal characterised in that the formulation also incorporates substituted or unsubstituted hydroxyl ammonium ions or hydrazine ions.
According to a second aspect of the present invention there is provided a method of cleaning aluminium surfaces in which the aluminium surface is treated with a cleaning formulation as defined in the previous paragraph.
The invention has been based on our finding that the use of substituted or unsubstituted hydroxyl ammonium or hydrazine ions provides significantly improved results in the cleaning of aluminium as compared to similar formulations which incorporate peroxide as an oxidising agent. More particularly, the use of such ions provides significantly improved removal of aluminium oxide from the surface of the aluminium. As such, cleaning formulations in accordance with the invention are particularly useful for the cleaning of aluminium can bodies produced by a drawing and ironing operation to effect removable thereof so that a good quality conversion coat may subsequently be applied. Such coated cans are not prone to dome-staining when subjected to a pasteurising operation. Whilst not wishing to be bound by theory, we believe that the significantly improved results are due to the effective removal of both organic and inorganic contaminants thus ensuring effective bonding of the conversion coating through elimination of a "de-wetting" or "masking" effect. This process is enhanced by the catalytic effect of the substituted or unsubstituted hydroxyl ammonium or hydrazine ions at the surface of the aluminium hydroxide. This enhancement allows the sulphuric acid in the formulation to etch the oxide layer. This etching effect also enhances the aesthetic appearance of the inside of containers by affecting the "grey scale" or "lightness" of the surface.
Formulations in accordance with the invention can be essentially fluoride-free. Additionally the formulations need not contain a peroxide, although we do not preclude the possibility of incorporating either compound (e.g. hydrogen peroxide or a fluoride).
Each component of the formulation, as defined for the first aspect of the invention, is preferably present in the amount indicated in the following table, with more preferred amounts for each component being given in the following description:
The amount of the substituted or unsubstituted hydroxyl ammonium or hydrazine ions present in the formulation is preferably in the range 0.0004 to 0.05%, more preferably 0.0004 to 0.02% and even more preferably 0.004 to 0.008% by weight of the formulation.
The substituted or unsubstituted hydroxyl ammonium or hydrazine ions may be introduced into the cleaning formulation in the form of salts or in the form of the corresponding free base, which is converted in situ in the acid conditions prevailing in the bath to the corresponding substituted or unsubstituted hydroxyl ammonium or hydrazine ions.
The hydroxyl ammonium or hydrazine ions may be of the formula H3XN+ where X is -OH, -NH2 or -NH3 +.
Preferably X is -OH, i.e. H3XN+ represents the hydroxyl ammonium ion. The formulation may, for example, be prepared from a hydroxyl ammonium salt which can incorporate a wide variety of anions, e.g. sulphate, phosphate, chloride, nitrate or bromide. It is however also possible to prepare the formulation from NH2OH which (as indicated above) is converted in situ in the acid conditions of the formulation to the hydroxyl ammonium ion.
It is preferred that the formulation is prepared from hydroxyl ammonium sulphate.
Substituted or unsubstituted hydrazine ions may be provided by sulphate, nitrate, nitro or chloride salts. Particular examples include phenyl hydrazine sulphate, p-nitro phenyl hydrazine, benzyl phenyl hydrazine, maleic hydrazine, hydrazine sulphate, hydrazine di-mono hydrochloride, 2,4-dinitrophenyl hydrazine, anthrone, dithizone, 1,2,3,4-tetrahydrocarbazole, dimethylglyoxime, and hydrazine nitrate.
The d-block transition metal ion is preferably present in the formulation in an amount 0.0001-0.015%, more preferably 0.003-0.006%.
The d-block transition metal ion may for example be provided by salts of iron, platinum, silver, gold, manganese, nickel or molybdenum.
The d-block transition metal ion is preferably the ferric ion (Fe3+).
Most conveniently, the ferric ion is provided by a ferric salt such as Fe2(SO4)3, Fe(NO3)2 orFe2(CO4)3.
Alternatively the ferric ions may be produced in situ from ferrous salts which are converted under the oxidising conditions of the cleaning formulation to provide the ferric ions.
The amount of aluminium sequestrant present in the formulation is preferably 0.005-0.25% by weight, more preferably 0.05-0.1%.
The aluminium sequestrant is preferably provided by at least one carboxylic acid. The carboxylic may be provided at least partly by a di- or higher- basic carboxylic acid. The acid may, for example, be of the formula HOOC (CEb)nCOOH with n preferably being from 0 to 4 so that the acid has a maximum of 6 carbon atoms, this being preferred to ensure that the di-basic acid (of the indicated formula) is water-soluble. It is however also possible to use di-basic acids that also incorporate at least one hydroxyl group to improve water solubility, in which case the acid may contain more than 6 carbon atoms.
The di-basic acid may be malonic acid, succinic acid or adipic acid. For preference, malonic or succinic acid are used.
We have also found that improved results for the cleaning formulation can be obtained if the sequestrant comprises a mixture of a di-basic acid of the formula HOOC(CH2)nCOOH (where n is as defined above) and a carboxylic acid (preferably a poly-basic carboxylic acid) containing a hydroxyl group. This latter acid may be a di- or higher- basic carboxylic acid (also containing a hydroxyl group) and is most preferably citric acid. The improved results obtained by the combination of these two acids reside in an improvement in the brightness of the interior of the can body after conversion coating.
Preferably the amount of acid of the formula HOOC(CH2)nCOOH in the formulation is in the range 0.02-0.06% as also is the amount of the hydroxycarboxylic acid (e.g. citric acid). It is particularly preferred that the amount of acid of the formula HOOC(CH2)nCOOH is in the range 0.02-0.04% whereas the amount of the hydroxycarboxylic acid is in the range 0.03-0.06%.
The cleaning formulation contains a total amount of 0.004-0.25% (more preferably 0.04-0.1%) of surface active agents. The surface active agents may be cationic, anionic, non-anionic or amphoteric agents, suitable examples of which are
disclosed in US-A-4 980 076 (Nihon Parkerizing). It is however particularly preferred that the surface active agents are non-ionic agents.
It is preferred that the surface active agent comprises at least one fatty alcohol ethoxylate. The or each such surfacactant may have an alcohol residue containing 8- 15 carbon atoms and may incorporate 4-15 moles of ethylene oxide (per mole of fatty alcohol residue). Preferably the surface active agent system comprises 0.01-0.04% by weight (based on the total weight of the cleaning formulation) of each of:
(i) a fatty alcohol (C13) ethoxylate with 8 moles of ethylene oxide (e.g. as available under the names Caflon TD0900 or Lutensol T08); and
(ii) a fatty alcohol (C10) ethoxylate with 4 moles of ethylene oxide (e.g. as available under the names Rhodaclean MSC or Lutensol XL40).
The surface active agent system preferably also includes a surface active agent incorporating polysaccharide (e.g. polyglucoside) residues. Such a surface active agent is preferably present in an amount 0.005-0.02% by weight of the formulation. Suitable surface active agents in this category are alkylated, ethoxylated or propoxylated polyglucosides. Alkyl polyglucosides are particularly preferred, in particular those in which the alkyl residue has a carbon chain length of C12-C16. The formulation may incorporate a defoamer, e.g. Pluronic PE6100.
The cleaning formulation further incorporates sulphuric acid, preferably in an amount of 0.05 to 1%, more preferably 0.1% to 0.5%, by weight (expressed as H2SO4) of the formulation.
The cleaning formulation of the invention has a pH of 0.5 to 5, more preferably 0.5 to 3.0, even more preferably 0.5 to 2.5.
Therefore, in summary, a preferred and even more preferred amounts for components of the cleaning formulation are as shown in the following table:
The cleaning operation (in accordance with the second aspect of the invention) may be carried out by immersing the can bodies in the cleaning formulation or alternatively by spraying the bodies with the formulation. Generally the cleaning formulation will be at a temperature of 20-80°C, more preferably 50-70°C. Generally the cleaning operation will be effected for a period of 10 to 120 seconds.
After being treated with the cleaning formulation, the aluminium may be washed with water.
A cleaning formulation in accordance with the invention may be prepared by admixing the individual components in the required amounts in water. Conveniently however a cleaning formulation in accordance with the invention is obtained by dilution of a pre-prepared concentrate. A typical concentrate formulation is as shown below:
As an alternative the above concentrate may be prepared without the sulphuric acid, in which case the concentrate and sulphuric acid are added separately to water to produce the final cleaning formulation. If the concentrate contains sulphuric acid then the amount is preferably in the range 15% to 25% by weight of the concentrate.
The aluminium sequestrant preferably comprises 1-5% by weight of a di-basic carboxylic acid of the formula HOOC(CH2)nCOOH, where n is 0 to 4 and 1-5% of a poly-basic acid containing a hydroxyl group. The sequestrant preferably comprises succinic or adipic acid and citric acid.
The surface active agent preferably comprises 0.5 to 2.5% by weight of each of:
(a) an alkyl polyglucoside;
(b) a fatty alcohol (C13) ethoxylate with 8 moles of ethylene oxide (e.g. as available under the names Caflon TD0900 or Lutensol T08); and
(c) a fatty alcohol (C1O) ethoxylate with 4 moles of ethylene oxide (e.g. as available under the names Rhodaclean MSC or Lutensol XL40).
The invention will be illustrated by reference to the following non-limiting Example and accompanying drawings which illustrate the results of the Example.
Example
The concentrate was prepared by heating the water to 250C and adding the succinic acid with thorough mixing. The remaining components were then added in the order listed with thorough mixing between additions and for one hour after addition of the final component.
The diluted concentrate was used for cleaning aluminium can bodies that had been produced by a standard drawing and ironing operation. Cleaning was effected by washing the cans (using the wash solution detailed above) in a household dishwasher for 3 minutes at 55°C to 60°C (low pressure). Sufficient amount of the concentrate was added to produce an approximately 1% solution of the cleaning formulation.
The cleaned cans were then subjected to a washing operation with water.
One can was then subjected to a "dome staining" test in which the can was immersed in a solution of borax (0.3 g I"1) at 800C for 20 minutes.
A further (cleaned) can was given a "conversion coat" using Houghto-Coat NC900 at a pH 2.9 for 40 seconds at 400C. The coated can was then subjected to the "dome-staining" test described above.
The results are shown in Fig 1 in which the left hand photograph is for the coated can.
Comparative Example
The procedure of Example 1 was repeated but using a peroxide-based cleaning formulation of the type described in PCT/GB 2004/002729 (Natech Ltd). The results are shown in Fig 2 in which the coated can is on the right hand side.
The improvements obtained by the present invention are evident from a comparison of Figs 1 and 2.
Claims
1. A cleaning formulation for cleaning aluminium surfaces, the formulation having a pH of 0.5 to 5 and incorporating sulphuric acid at least one aluminium sequestrant, at least one surface active agent and ions of at least one d- block transition metal characterised in that the formulation also incorporates substituted or unsubstituted hydroxyl ammonium ions or hydrazine ions.
2. A formulation as claimed in claim 1 comprising 0.0004-0.05% by weight of said hydroxyl ammonium or hydrazine ions.
3. A formulation as claimed in claim 2 containing 0.004-0.008% by weight of said hydroxyl ammonium or hydrazine ions.
4. A formulation as claimed in any one of claims 1 to 3 wherein said hydroxyl ammonium ions are of the formula KbXINrNvhere is X -OH.
5. A formulation as claimed in any one of claims 1 to 4 comprising 0.005-0.25% by weight total of aluminium sequestrant.
6. A formulation as claimed in claim 5 comprising 0.05-0.1% by weight total of aluminium sequestrant.
7. A formulation as claimed in any one of claims 1 to 6 wherein the aluminium sequestrant comprises an acid of the formula HOOC(CH2)nCOOH where n is from 0 to 4 and a carboxylic acid containing a hydroxyl group.
8. A formulation as claimed in claim 7 wherein the aluminium sequestrant comprises succinic acid and citric acid.
9. A formulation as claimed in any one of claims 1 to 8 containing 0.004- 0.25% by weight total of at least one surface active agent.
10. A formulation as claimed in claim 9 containing 0.04-0.1% by weight total of surface active agents.
11. A formulation as claimed in claim 10 wherein the surface active agent comprises at least one alcohol ethoxylate having an alcohol residue containing 8-15 carbon atoms and incorporating 4-15 moles of ethylene oxide (per mole of alcohol residue).
12. A formulation as claimed in claim 10 or 11 which includes an alkyl polyglucoside as an non-ionic surface active agent.
13. A formulation as claimed in claim 12 wherein the alkyl polyglucoside is a C12 -C16 -alkyl polyglucoside.
14. A formulation as claimed in any one of claims 1 to 13 wherein the d- block transition metal ion is present in the formulation in an amount of 0.0001- 0.015%.
15. A formulation as claimed in claim 14 wherein the d-block transition metal ion is present in the formulation in an amount of 0.003-0.006%.
16. A formulation as claimed in any one of claims 1 to 15 wherein the transition metal ion is the ferric ion.
17. A formulation as claimed in claim 1 comprising:
18. A method of cleaning an article having an aluminium surface, the method comprising treating the article with a cleaning formulation as claimed in any one of claims 1 to 17.
19. A concentrate for dilution to a cleaning formulation, the concentrate comprising:
20. A concentrate as claimed in claim 19, wherein the aluminium sequestrant comprises 1-5% by weight of dye-basic carboxylic acid of the formula HOOC(CH2)nCOOH, where n is 0 to 4 and 1-5% of a poly-basic acid containing a hydroxyl group.
21. A concentrate as claimed in claim 19 or 20 wherein the sequestrant comprises (i) malonic, succinnic or adipic acid and (u) citric acid.
22. A concentrate as claimed in any one of claims 19 to 21, wherein the surface active agent comprises 0.5 to 2.5% by weight of each of:
(a) an alkyl polyglucoside;
(b) a fatty alcohol (C13) ethoxylate with 8 moles of ethylene oxide (i); and
(c) a fatty alcohol (C1Q) ethoxylate with 4 moles of ethylene oxide.
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
GBGB0500071.6A GB0500071D0 (en) | 2005-01-05 | 2005-01-05 | Cleaning formulation |
GB0500071.6 | 2005-01-05 |
Publications (1)
Publication Number | Publication Date |
---|---|
WO2006072780A1 true WO2006072780A1 (en) | 2006-07-13 |
Family
ID=34179165
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
PCT/GB2006/000015 WO2006072780A1 (en) | 2005-01-05 | 2006-01-04 | Cleaning formulation |
Country Status (2)
Country | Link |
---|---|
GB (1) | GB0500071D0 (en) |
WO (1) | WO2006072780A1 (en) |
Cited By (3)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
EP2221357A1 (en) * | 2009-02-19 | 2010-08-25 | Budich International GmbH | Combined limescale remover and rinser for use in devices and assemblies with metallic, ceramic, glass or plastic surfaces |
WO2014118053A1 (en) * | 2013-02-01 | 2014-08-07 | Cognis Ip Management Gmbh | Cleaning compositions comprising low hlb 2-propyl heptyl alcohol alkoxylates and alkyl polyglucosides |
EP3456864A1 (en) * | 2017-09-18 | 2019-03-20 | Henkel AG & Co. KGaA | Two stage pre-treatment of aluminium, in particular aluminium casting alloys, comprising a pickle and a conversion treatment |
Citations (4)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
GB919493A (en) * | 1957-04-06 | 1963-02-27 | Siemens Ag | Method of pickling iron-containing surfaces |
US4851148A (en) * | 1985-04-04 | 1989-07-25 | Amchem Products, Inc. | Method of controlling an aluminum surface cleaning composition |
US4980076A (en) * | 1988-09-07 | 1990-12-25 | Nihon Parkerizing Co., Ltd. | Fluoride and chromium free acid etchant rinse for aluminum |
EP0789094A1 (en) * | 1994-10-21 | 1997-08-13 | Nippon Paint Co., Ltd. | Aqueous acid cleaning solution for aluminum metal and method for cleaning the metal |
-
2005
- 2005-01-05 GB GBGB0500071.6A patent/GB0500071D0/en not_active Ceased
-
2006
- 2006-01-04 WO PCT/GB2006/000015 patent/WO2006072780A1/en not_active Application Discontinuation
Patent Citations (4)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
GB919493A (en) * | 1957-04-06 | 1963-02-27 | Siemens Ag | Method of pickling iron-containing surfaces |
US4851148A (en) * | 1985-04-04 | 1989-07-25 | Amchem Products, Inc. | Method of controlling an aluminum surface cleaning composition |
US4980076A (en) * | 1988-09-07 | 1990-12-25 | Nihon Parkerizing Co., Ltd. | Fluoride and chromium free acid etchant rinse for aluminum |
EP0789094A1 (en) * | 1994-10-21 | 1997-08-13 | Nippon Paint Co., Ltd. | Aqueous acid cleaning solution for aluminum metal and method for cleaning the metal |
Cited By (8)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
EP2221357A1 (en) * | 2009-02-19 | 2010-08-25 | Budich International GmbH | Combined limescale remover and rinser for use in devices and assemblies with metallic, ceramic, glass or plastic surfaces |
WO2014118053A1 (en) * | 2013-02-01 | 2014-08-07 | Cognis Ip Management Gmbh | Cleaning compositions comprising low hlb 2-propyl heptyl alcohol alkoxylates and alkyl polyglucosides |
US20140221268A1 (en) * | 2013-02-01 | 2014-08-07 | Cognis Ip Management Gmbh | Cleaning Compositions Comprising Low HLB 2-Propyl Heptyl Alcohol Alkoxylates And Alkyl Polyglucosides |
US9120998B2 (en) * | 2013-02-01 | 2015-09-01 | Cognis Ip Management Gmbh | Cleaning compositions comprising low HLB 2-propyl heptyl alcohol alkoxylates and alkyl polyglucosides |
CN105102601A (en) * | 2013-02-01 | 2015-11-25 | 考格尼斯知识产权管理有限责任公司 | Cleaning compositions comprising low hlb 2-propyl heptyl alcohol alkoxylates and alkyl polyglucosides |
EP3456864A1 (en) * | 2017-09-18 | 2019-03-20 | Henkel AG & Co. KGaA | Two stage pre-treatment of aluminium, in particular aluminium casting alloys, comprising a pickle and a conversion treatment |
WO2019052701A1 (en) * | 2017-09-18 | 2019-03-21 | Henkel Ag & Co. Kgaa | Two-stage pre-treatment of aluminum, in particular aluminum casting alloys, comprising pickle and conversion treatment |
US11499237B2 (en) | 2017-09-18 | 2022-11-15 | Henkel Ag & Co. Kgaa | Two-stage pretreatment of aluminum, in particular aluminum casting alloys, comprising pickle and conversion treatment |
Also Published As
Publication number | Publication date |
---|---|
GB0500071D0 (en) | 2005-02-09 |
Similar Documents
Publication | Publication Date | Title |
---|---|---|
US7709435B2 (en) | Alkaline cleaning liquid comprising metallic ions for aluminum or aluminum alloys and method of cleaning | |
US7947333B2 (en) | Method for coating of metallic coil or sheets for producing hollow articles | |
US4599116A (en) | Alkaline cleaning process | |
US4313769A (en) | Coating solution for metal surfaces | |
KR101537146B1 (en) | Composition for the alkaline passivation of zinc surfaces | |
CA1182389A (en) | Non-fluoride acid compositions for cleaning aluminum surfaces | |
US4540444A (en) | Aluminum cleaner and system | |
MXPA97007196A (en) | Cleaning agent protector of the corrosion paraacero chapado de est | |
US10392710B2 (en) | Brightening and passivation of stainless steel surfaces | |
JPS61157688A (en) | Degreasing and cleaning agent for tin and tinned surface | |
US5437740A (en) | Corrosion resistant aluminum and aluminum coating | |
KR101977807B1 (en) | Method for anodizing surface treatment of automotive sunroof rails | |
US5227016A (en) | Process and composition for desmutting surfaces of aluminum and its alloys | |
WO2006072780A1 (en) | Cleaning formulation | |
US3951681A (en) | Method for descaling ferrous metals | |
EP0032306B1 (en) | Aluminium-coating solution, process and concentrate | |
JP2002505378A (en) | Aqueous solution and method for phosphating metal surfaces | |
CA1284451C (en) | Solution and process for cold forming titanium | |
JPH04218681A (en) | Treatment of surface on formed material combining aluminum and steel material and treating solution | |
JPS63286585A (en) | Chemical treating solution for titanium or alloy thereof and surface treatment of titanium or alloy thereof with said solution | |
JPH02153074A (en) | Dipping-solution for coating tin and coating-method by dipping using its solution | |
JP4778769B2 (en) | Aluminum can manufacturing method and aluminum can manufactured by the method | |
US7041629B2 (en) | Stripper for special steel | |
US6695927B1 (en) | Method and cleaning solution for cleaning a container | |
JP2002220678A (en) | Treatment method for hot-rolled steel sheet or steel material, and hot-rolled steel sheet or steel material |
Legal Events
Date | Code | Title | Description |
---|---|---|---|
121 | Ep: the epo has been informed by wipo that ep was designated in this application | ||
NENP | Non-entry into the national phase |
Ref country code: DE |
|
122 | Ep: pct application non-entry in european phase |
Ref document number: 06701721 Country of ref document: EP Kind code of ref document: A1 |
|
WWW | Wipo information: withdrawn in national office |
Ref document number: 6701721 Country of ref document: EP |