EP0312176B1 - Verfahren zum Aufbringen von Konversionsüberzügen - Google Patents
Verfahren zum Aufbringen von Konversionsüberzügen Download PDFInfo
- Publication number
- EP0312176B1 EP0312176B1 EP88202291A EP88202291A EP0312176B1 EP 0312176 B1 EP0312176 B1 EP 0312176B1 EP 88202291 A EP88202291 A EP 88202291A EP 88202291 A EP88202291 A EP 88202291A EP 0312176 B1 EP0312176 B1 EP 0312176B1
- Authority
- EP
- European Patent Office
- Prior art keywords
- tin
- solution
- coating
- treatment
- conversion
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Expired - Lifetime
Links
- 238000007739 conversion coating Methods 0.000 title claims description 28
- 238000000034 method Methods 0.000 title claims description 18
- ATJFFYVFTNAWJD-UHFFFAOYSA-N Tin Chemical compound [Sn] ATJFFYVFTNAWJD-UHFFFAOYSA-N 0.000 claims description 24
- 239000005028 tinplate Substances 0.000 claims description 14
- 229910052751 metal Inorganic materials 0.000 claims description 9
- 239000002184 metal Substances 0.000 claims description 9
- NBIIXXVUZAFLBC-UHFFFAOYSA-K phosphate Chemical compound [O-]P([O-])([O-])=O NBIIXXVUZAFLBC-UHFFFAOYSA-K 0.000 claims description 9
- XTEGARKTQYYJKE-UHFFFAOYSA-M Chlorate Chemical compound [O-]Cl(=O)=O XTEGARKTQYYJKE-UHFFFAOYSA-M 0.000 claims description 6
- 239000007864 aqueous solution Substances 0.000 claims description 4
- SXDBWCPKPHAZSM-UHFFFAOYSA-M bromate Inorganic materials [O-]Br(=O)=O SXDBWCPKPHAZSM-UHFFFAOYSA-M 0.000 claims description 3
- SXDBWCPKPHAZSM-UHFFFAOYSA-N bromic acid Chemical compound OBr(=O)=O SXDBWCPKPHAZSM-UHFFFAOYSA-N 0.000 claims description 3
- 229920000137 polyphosphoric acid Polymers 0.000 claims description 2
- 150000003839 salts Chemical class 0.000 claims description 2
- 239000003795 chemical substances by application Substances 0.000 claims 2
- 239000000243 solution Substances 0.000 description 35
- 229910052718 tin Inorganic materials 0.000 description 23
- HEMHJVSKTPXQMS-UHFFFAOYSA-M sodium hydroxide Substances [OH-].[Na+] HEMHJVSKTPXQMS-UHFFFAOYSA-M 0.000 description 20
- 229910019142 PO4 Inorganic materials 0.000 description 18
- 238000005260 corrosion Methods 0.000 description 14
- 230000007797 corrosion Effects 0.000 description 14
- 238000000576 coating method Methods 0.000 description 12
- 239000011248 coating agent Substances 0.000 description 11
- NBIIXXVUZAFLBC-UHFFFAOYSA-N Phosphoric acid Chemical compound OP(O)(O)=O NBIIXXVUZAFLBC-UHFFFAOYSA-N 0.000 description 10
- 235000021317 phosphate Nutrition 0.000 description 9
- 239000008139 complexing agent Substances 0.000 description 8
- 235000011007 phosphoric acid Nutrition 0.000 description 8
- 230000015572 biosynthetic process Effects 0.000 description 7
- 239000010452 phosphate Substances 0.000 description 6
- 238000005554 pickling Methods 0.000 description 6
- 229910001432 tin ion Inorganic materials 0.000 description 6
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 6
- 229910021627 Tin(IV) chloride Inorganic materials 0.000 description 5
- 230000000052 comparative effect Effects 0.000 description 5
- 239000003973 paint Substances 0.000 description 5
- HPGGPRDJHPYFRM-UHFFFAOYSA-J tin(iv) chloride Chemical compound Cl[Sn](Cl)(Cl)Cl HPGGPRDJHPYFRM-UHFFFAOYSA-J 0.000 description 5
- DGAQECJNVWCQMB-PUAWFVPOSA-M Ilexoside XXIX Chemical compound C[C@@H]1CC[C@@]2(CC[C@@]3(C(=CC[C@H]4[C@]3(CC[C@@H]5[C@@]4(CC[C@@H](C5(C)C)OS(=O)(=O)[O-])C)C)[C@@H]2[C@]1(C)O)C)C(=O)O[C@H]6[C@@H]([C@H]([C@@H]([C@H](O6)CO)O)O)O.[Na+] DGAQECJNVWCQMB-PUAWFVPOSA-M 0.000 description 4
- ZLMJMSJWJFRBEC-UHFFFAOYSA-N Potassium Chemical compound [K] ZLMJMSJWJFRBEC-UHFFFAOYSA-N 0.000 description 4
- 230000008021 deposition Effects 0.000 description 4
- KRKNYBCHXYNGOX-UHFFFAOYSA-N citric acid Chemical compound OC(=O)CC(O)(C(O)=O)CC(O)=O KRKNYBCHXYNGOX-UHFFFAOYSA-N 0.000 description 3
- 150000002500 ions Chemical class 0.000 description 3
- JEIPFZHSYJVQDO-UHFFFAOYSA-N iron(III) oxide Inorganic materials O=[Fe]O[Fe]=O JEIPFZHSYJVQDO-UHFFFAOYSA-N 0.000 description 3
- 150000003013 phosphoric acid derivatives Chemical class 0.000 description 3
- 229910052700 potassium Inorganic materials 0.000 description 3
- 229910052708 sodium Inorganic materials 0.000 description 3
- FQENQNTWSFEDLI-UHFFFAOYSA-J sodium diphosphate Chemical compound [Na+].[Na+].[Na+].[Na+].[O-]P([O-])(=O)OP([O-])([O-])=O FQENQNTWSFEDLI-UHFFFAOYSA-J 0.000 description 3
- VHUUQVKOLVNVRT-UHFFFAOYSA-N Ammonium hydroxide Chemical compound [NH4+].[OH-] VHUUQVKOLVNVRT-UHFFFAOYSA-N 0.000 description 2
- VEXZGXHMUGYJMC-UHFFFAOYSA-M Chloride anion Chemical compound [Cl-] VEXZGXHMUGYJMC-UHFFFAOYSA-M 0.000 description 2
- VEXZGXHMUGYJMC-UHFFFAOYSA-N Hydrochloric acid Chemical compound Cl VEXZGXHMUGYJMC-UHFFFAOYSA-N 0.000 description 2
- XEEYBQQBJWHFJM-UHFFFAOYSA-N Iron Chemical compound [Fe] XEEYBQQBJWHFJM-UHFFFAOYSA-N 0.000 description 2
- QAOWNCQODCNURD-UHFFFAOYSA-N Sulfuric acid Chemical compound OS(O)(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-N 0.000 description 2
- 229910021626 Tin(II) chloride Inorganic materials 0.000 description 2
- 239000002390 adhesive tape Substances 0.000 description 2
- 239000003513 alkali Substances 0.000 description 2
- 229910000147 aluminium phosphate Inorganic materials 0.000 description 2
- 239000000908 ammonium hydroxide Substances 0.000 description 2
- 229910052799 carbon Inorganic materials 0.000 description 2
- XLYOFNOQVPJJNP-ZSJDYOACSA-N heavy water Substances [2H]O[2H] XLYOFNOQVPJJNP-ZSJDYOACSA-N 0.000 description 2
- 239000011591 potassium Substances 0.000 description 2
- KWYUFKZDYYNOTN-UHFFFAOYSA-M potassium hydroxide Substances [OH-].[K+] KWYUFKZDYYNOTN-UHFFFAOYSA-M 0.000 description 2
- 239000002244 precipitate Substances 0.000 description 2
- 238000001556 precipitation Methods 0.000 description 2
- 239000011734 sodium Substances 0.000 description 2
- 235000019832 sodium triphosphate Nutrition 0.000 description 2
- 229910001220 stainless steel Inorganic materials 0.000 description 2
- 235000011150 stannous chloride Nutrition 0.000 description 2
- AXZWODMDQAVCJE-UHFFFAOYSA-L tin(II) chloride (anhydrous) Chemical compound [Cl-].[Cl-].[Sn+2] AXZWODMDQAVCJE-UHFFFAOYSA-L 0.000 description 2
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 description 1
- 229920000298 Cellophane Polymers 0.000 description 1
- LZZYPRNAOMGNLH-UHFFFAOYSA-M Cetrimonium bromide Chemical compound [Br-].CCCCCCCCCCCCCCCC[N+](C)(C)C LZZYPRNAOMGNLH-UHFFFAOYSA-M 0.000 description 1
- 206010013786 Dry skin Diseases 0.000 description 1
- 239000004593 Epoxy Substances 0.000 description 1
- 229910001335 Galvanized steel Inorganic materials 0.000 description 1
- 229910002651 NO3 Inorganic materials 0.000 description 1
- NHNBFGGVMKEFGY-UHFFFAOYSA-N Nitrate Chemical compound [O-][N+]([O-])=O NHNBFGGVMKEFGY-UHFFFAOYSA-N 0.000 description 1
- 229910000831 Steel Inorganic materials 0.000 description 1
- XSQUKJJJFZCRTK-UHFFFAOYSA-N Urea Chemical compound NC(N)=O XSQUKJJJFZCRTK-UHFFFAOYSA-N 0.000 description 1
- 230000001133 acceleration Effects 0.000 description 1
- 239000003929 acidic solution Substances 0.000 description 1
- 230000002730 additional effect Effects 0.000 description 1
- 239000004202 carbamide Substances 0.000 description 1
- 150000004697 chelate complex Chemical class 0.000 description 1
- 239000002738 chelating agent Substances 0.000 description 1
- 238000006243 chemical reaction Methods 0.000 description 1
- XTEGARKTQYYJKE-UHFFFAOYSA-N chloric acid Chemical compound OCl(=O)=O XTEGARKTQYYJKE-UHFFFAOYSA-N 0.000 description 1
- 150000001805 chlorine compounds Chemical class 0.000 description 1
- 238000004140 cleaning Methods 0.000 description 1
- 230000000536 complexating effect Effects 0.000 description 1
- 238000010668 complexation reaction Methods 0.000 description 1
- 239000000470 constituent Substances 0.000 description 1
- 239000008367 deionised water Substances 0.000 description 1
- 229910021641 deionized water Inorganic materials 0.000 description 1
- MNNHAPBLZZVQHP-UHFFFAOYSA-N diammonium hydrogen phosphate Chemical compound [NH4+].[NH4+].OP([O-])([O-])=O MNNHAPBLZZVQHP-UHFFFAOYSA-N 0.000 description 1
- 229910000388 diammonium phosphate Inorganic materials 0.000 description 1
- 235000019838 diammonium phosphate Nutrition 0.000 description 1
- NBIIXXVUZAFLBC-UHFFFAOYSA-M dihydrogenphosphate Chemical compound OP(O)([O-])=O NBIIXXVUZAFLBC-UHFFFAOYSA-M 0.000 description 1
- 235000019797 dipotassium phosphate Nutrition 0.000 description 1
- 229910000396 dipotassium phosphate Inorganic materials 0.000 description 1
- 229910000397 disodium phosphate Inorganic materials 0.000 description 1
- 235000019800 disodium phosphate Nutrition 0.000 description 1
- TVQLLNFANZSCGY-UHFFFAOYSA-N disodium;dioxido(oxo)tin Chemical compound [Na+].[Na+].[O-][Sn]([O-])=O TVQLLNFANZSCGY-UHFFFAOYSA-N 0.000 description 1
- 238000001035 drying Methods 0.000 description 1
- 230000000694 effects Effects 0.000 description 1
- 230000002349 favourable effect Effects 0.000 description 1
- 239000008397 galvanized steel Substances 0.000 description 1
- 239000010439 graphite Substances 0.000 description 1
- 229910002804 graphite Inorganic materials 0.000 description 1
- 238000007654 immersion Methods 0.000 description 1
- 229910052742 iron Inorganic materials 0.000 description 1
- 150000004715 keto acids Chemical class 0.000 description 1
- 239000000463 material Substances 0.000 description 1
- 229910021645 metal ion Inorganic materials 0.000 description 1
- 238000012544 monitoring process Methods 0.000 description 1
- 238000010422 painting Methods 0.000 description 1
- HWGNBUXHKFFFIH-UHFFFAOYSA-I pentasodium;[oxido(phosphonatooxy)phosphoryl] phosphate Chemical compound [Na+].[Na+].[Na+].[Na+].[Na+].[O-]P([O-])(=O)OP([O-])(=O)OP([O-])([O-])=O HWGNBUXHKFFFIH-UHFFFAOYSA-I 0.000 description 1
- XUXNAKZDHHEHPC-UHFFFAOYSA-M sodium bromate Chemical compound [Na+].[O-]Br(=O)=O XUXNAKZDHHEHPC-UHFFFAOYSA-M 0.000 description 1
- 229940079864 sodium stannate Drugs 0.000 description 1
- 238000005507 spraying Methods 0.000 description 1
- 239000010935 stainless steel Substances 0.000 description 1
- 239000010959 steel Substances 0.000 description 1
- 150000003467 sulfuric acid derivatives Chemical class 0.000 description 1
- 239000008399 tap water Substances 0.000 description 1
- 235000020679 tap water Nutrition 0.000 description 1
- VKFFEYLSKIYTSJ-UHFFFAOYSA-N tetraazanium;phosphonato phosphate Chemical compound [NH4+].[NH4+].[NH4+].[NH4+].[O-]P([O-])(=O)OP([O-])([O-])=O VKFFEYLSKIYTSJ-UHFFFAOYSA-N 0.000 description 1
- UNXRWKVEANCORM-UHFFFAOYSA-I triphosphate(5-) Chemical compound [O-]P([O-])(=O)OP([O-])(=O)OP([O-])([O-])=O UNXRWKVEANCORM-UHFFFAOYSA-I 0.000 description 1
- LRXTYHSAJDENHV-UHFFFAOYSA-H zinc phosphate Chemical compound [Zn+2].[Zn+2].[Zn+2].[O-]P([O-])([O-])=O.[O-]P([O-])([O-])=O LRXTYHSAJDENHV-UHFFFAOYSA-H 0.000 description 1
- MFXMOUUKFMDYLM-UHFFFAOYSA-L zinc;dihydrogen phosphate Chemical compound [Zn+2].OP(O)([O-])=O.OP(O)([O-])=O MFXMOUUKFMDYLM-UHFFFAOYSA-L 0.000 description 1
Classifications
-
- 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
- C23C—COATING METALLIC MATERIAL; COATING MATERIAL WITH METALLIC MATERIAL; SURFACE TREATMENT OF METALLIC MATERIAL BY DIFFUSION INTO THE SURFACE, BY CHEMICAL CONVERSION OR SUBSTITUTION; COATING BY VACUUM EVAPORATION, BY SPUTTERING, BY ION IMPLANTATION OR BY CHEMICAL VAPOUR DEPOSITION, IN GENERAL
- C23C22/00—Chemical surface treatment of metallic material by reaction of the surface with a reactive liquid, leaving reaction products of surface material in the coating, e.g. conversion coatings, passivation of metals
- C23C22/05—Chemical surface treatment of metallic material by reaction of the surface with a reactive liquid, leaving reaction products of surface material in the coating, e.g. conversion coatings, passivation of metals using aqueous solutions
- C23C22/06—Chemical surface treatment of metallic material by reaction of the surface with a reactive liquid, leaving reaction products of surface material in the coating, e.g. conversion coatings, passivation of metals using aqueous solutions using aqueous acidic solutions with pH less than 6
- C23C22/07—Chemical surface treatment of metallic material by reaction of the surface with a reactive liquid, leaving reaction products of surface material in the coating, e.g. conversion coatings, passivation of metals using aqueous solutions using aqueous acidic solutions with pH less than 6 containing phosphates
- C23C22/08—Orthophosphates
- C23C22/10—Orthophosphates containing oxidants
-
- 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
- C23C—COATING METALLIC MATERIAL; COATING MATERIAL WITH METALLIC MATERIAL; SURFACE TREATMENT OF METALLIC MATERIAL BY DIFFUSION INTO THE SURFACE, BY CHEMICAL CONVERSION OR SUBSTITUTION; COATING BY VACUUM EVAPORATION, BY SPUTTERING, BY ION IMPLANTATION OR BY CHEMICAL VAPOUR DEPOSITION, IN GENERAL
- C23C22/00—Chemical surface treatment of metallic material by reaction of the surface with a reactive liquid, leaving reaction products of surface material in the coating, e.g. conversion coatings, passivation of metals
- C23C22/05—Chemical surface treatment of metallic material by reaction of the surface with a reactive liquid, leaving reaction products of surface material in the coating, e.g. conversion coatings, passivation of metals using aqueous solutions
- C23C22/06—Chemical surface treatment of metallic material by reaction of the surface with a reactive liquid, leaving reaction products of surface material in the coating, e.g. conversion coatings, passivation of metals using aqueous solutions using aqueous acidic solutions with pH less than 6
- C23C22/07—Chemical surface treatment of metallic material by reaction of the surface with a reactive liquid, leaving reaction products of surface material in the coating, e.g. conversion coatings, passivation of metals using aqueous solutions using aqueous acidic solutions with pH less than 6 containing phosphates
- C23C22/23—Condensed phosphates
-
- C—CHEMISTRY; METALLURGY
- C25—ELECTROLYTIC OR ELECTROPHORETIC PROCESSES; APPARATUS THEREFOR
- C25D—PROCESSES FOR THE ELECTROLYTIC OR ELECTROPHORETIC PRODUCTION OF COATINGS; ELECTROFORMING; APPARATUS THEREFOR
- C25D11/00—Electrolytic coating by surface reaction, i.e. forming conversion layers
- C25D11/36—Phosphatising
Definitions
- a disadvantage of using these known solutions is that when the treatment systems are at a standstill, the tin content in the solution drops, so that conversion coatings of inferior quality are produced when the system is restarted, unless an additional addition of tin to the treatment solution is carried out beforehand.
- a method for cathodic deposition of a phosphate coating on stainless steels in which a phosphating solution is used which contains a chelating agent, such as condensed phosphates.
- the object of the invention is to provide a process for applying conversion coatings on tinplate which does not have the disadvantages of the known processes and which, with small tin deposits, leads to conversion coatings with excellent corrosion resistance and precludes a decrease in the tin concentration in the treatment solution when the treatment systems are at a standstill.
- the complexing agent content suppressed the tin precipitation from the treatment solution, but at the same time its deposition on the workpiece surface when the Conversion overlay is not prevented.
- the complexing agent also accelerates the pickling attack on the metal surface and is responsible for a balance between the tin which dissolves (as a result of the pickling attack) and the tin which deposits as a coating component. This largely avoids fluctuations in the tin concentration in the treatment solution, which ultimately has a favorable effect on the quality, in particular the high corrosion resistance of the conversion coating.
- the phosphate can be introduced as an alkali phosphate, such as sodium, potassium or ammonium monohydrogen phosphate or dihydrogen phosphate. It can also be formed from phosphoric acid and sodium, potassium or ammonium hydroxide. Solutions with phosphate concentrations outside the range of 1 to 50 g / l are unable to produce conversion coatings with the desired excellent properties. Concentrations within the range of 2 to 25 g / l lead to particularly high-quality conversion coatings.
- the chlorides and / or sulfates of divalent or tetravalent tin can be used in particular as the source of tin ions.
- Sodium stannate is also suitable.
- the range from 0.01 to 5 g / l applies to tin II or tin IV ions, or to the sum of tin II and tin IV ions.
- Concentrations below 0.01 g / l reduce the corrosion resistance of the conversion coatings produced.
- concentrations above 5 g / l there is a risk that the treatment solution will become unstable. An additional improvement in the coating quality is also not achieved.
- Complexing agents are sodium, potassium or ammonium pyrophosphate, tripolyphosphate or tetrapolyphosphate. At concentrations below 0.01 g / l, the complexing effect of the condensed phosphates is no longer sufficiently pronounced, i.e. the ability to prevent tin precipitation is waning. With concentrations above 5 g / l, an excessive pickling attack on the metal surface can be associated, in particular, the deposition of the tin in the conversion coating can be hindered.
- phosphoric acid hydrochloric acid, sulfuric acid or sodium, potassium or ammonium hydroxide is expediently used.
- the pH range to be set from 2 to 6 is important insofar as the corrosion resistance of the conversion coating formed becomes low at a pH value below 2 and the tendency at a pH value above 6 that tin ions precipitate out of the solution and therefore proper coating formation is no longer guaranteed.
- the conversion coating is formed electrochemically.
- This embodiment is particularly advantageous for the treatment of strip material made of tinplate.
- the corrosion resistance of the conversion coating formed is particularly high.
- the tinplate is switched as the anode against graphite, stainless steel and the like as the cathode, an electrode spacing of approximately 10 to 500 mm and a current density of approximately 0.1 A / dm 2 are set for a period of 0.5 to 60 s. Direct or alternating current can be used.
- the conversion coating is produced in two stages, first chemically, then electrochemically. This will increase the corrosion resistance again achieved.
- Tin-II or tin-IV and phosphate are the essential constituents forming the conversion coating.
- the layer formation begins with the pickling attack of the acidic solution on the metal surface. It is intensified by the action of the accelerators, especially the oxo acids.
- the complexing agent controls the tin deposition by forming a chelate complex with tin, which would otherwise easily precipitate out of the treatment solution, and provides the tin ions required for coating formation in a controlled manner.
- Another role of the complexing agent is to bind the metal ions released from the metal surface by the pickling attack and to make them available again in a controlled manner for coating formation.
- the complexing agent is responsible for uniform coating formation by influencing the pickling attack.
- the coatings also have excellent properties as the basis for subsequent painting, printing and the like in terms of corrosion resistance, adhesion and gloss.
- the treatment solution experiences practically no reduction in the tin content even after long downtimes, so that the process can then be resumed immediately and perfect conversion coatings are immediately obtained.
- Cans made from tinplate were cleaned in a mildly alkaline cleaner with a concentration of 1% by weight in water. The coating was then sprayed for 20 s using the solutions listed below. After a water rinse, deionized water of a quality of at least 300,000 ohm ⁇ cm was sprayed for a period of 10 s and then dried in a hot air oven at 200 ° C. within 3 minutes. The conversion coating was applied in each case with a freshly prepared coating solution and one which had stood for one day for 10 cans per liter of solution.
- H3PO4 (75% by weight) 15 g / l (PO4 11 g / l) NaClO3 6 g / l SnCl4 ⁇ 5H2O 0.6 g / l (Sn 0.2 g / l) Na4P2O7 ⁇ 10H2O 1.5 g / l (P2O7 0.6 g / l) pH 3.1 adjusted with sodium hydroxide solution
- Tinplate cans were treated according to the procedure described in Example 1 with the following solution: H3PO4 (75% by weight) 2.8 g / l (PO4 2 g / l) NaClO3 0.3 g / l SnCl2 ⁇ 2H2O 0.04 g / l (Sn 0.02 g / l) Na4P2O7 ⁇ 10H2O 0.05 g / l (P2O7 0.02 g / l) pH 5.7 adjusted with sodium hydroxide solution Treatment temperature 70 ° C
- tinplate cans were treated with the following solution: H3PO4 (75% by weight) 55 g / l (PO4 40 g / l) NaBrO3 17 g / l SnCl4 ⁇ 5H2O 13.2 g / l (Sn 4.5 g / l) Na5P3O10 6.5 g / l (P3O10 4.5 g / l) pH 2.2 adjusted with sodium hydroxide solution Treatment temperature 60 ° C
- tinplate cans were treated with the following solution: H3PO4 (75% by weight) 15 g / l (PO4 11 g / l) NaClO3 6 g / l SnCl4 ⁇ 5H2O 0.6 g / l (Sn 0.2 g / l) Na4P2O7 ⁇ 10H2O 21 g / l (P2O7 8 g / l) pH 3.1 adjusted with sodium hydroxide solution Treatment temperature 60 ° C
- the tin content was determined after the batch and after standing for one day.
- the tinplate cans provided with conversion coatings were subjected to the corrosion test and the paint adhesion test.
- the treated cans were immersed in tap water at 60 ° C. for 30 minutes and the rust development was assessed.
- an epoxy / urea paint with a thickness of 5 to 7 ⁇ m was applied to the cans provided with the conversion coatings and baked at 210 ° C. (duration 10 minutes). After standing for 24 hours, the cans were immersed in a 1% by weight aqueous citric acid solution at 95 to 97 ° C and left therein for 60 minutes. It was then rinsed with water and dried.
- the samples were provided with a cross cut reaching to the metal surface and then with cellophane adhesive tape by pressing firmly. After the adhesive tape was torn off, it was found that the paint adhesion was consistently excellent, i.e. no paint detachment was found.
Landscapes
- Chemical & Material Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Engineering & Computer Science (AREA)
- Materials Engineering (AREA)
- Metallurgy (AREA)
- Organic Chemistry (AREA)
- General Chemical & Material Sciences (AREA)
- Mechanical Engineering (AREA)
- Electrochemistry (AREA)
- Chemical Treatment Of Metals (AREA)
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP62257678A JPH01100281A (ja) | 1987-10-13 | 1987-10-13 | 金属表面の皮膜化成処理液 |
JP257678/87 | 1987-10-13 |
Publications (2)
Publication Number | Publication Date |
---|---|
EP0312176A1 EP0312176A1 (de) | 1989-04-19 |
EP0312176B1 true EP0312176B1 (de) | 1992-12-16 |
Family
ID=17309584
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
EP88202291A Expired - Lifetime EP0312176B1 (de) | 1987-10-13 | 1988-10-13 | Verfahren zum Aufbringen von Konversionsüberzügen |
Country Status (10)
Country | Link |
---|---|
US (1) | US4927472A (pt) |
EP (1) | EP0312176B1 (pt) |
JP (1) | JPH01100281A (pt) |
AU (1) | AU608374B2 (pt) |
BR (1) | BR8805286A (pt) |
CA (1) | CA1321859C (pt) |
DE (2) | DE3834480A1 (pt) |
GB (1) | GB2210900B (pt) |
MX (1) | MX169760B (pt) |
ZA (1) | ZA887663B (pt) |
Families Citing this family (28)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US5370909A (en) * | 1990-06-19 | 1994-12-06 | Henkel Corporation | Liquid composition and process for treating aluminum or tin cans to impart corrosion resistance and mobility thereto |
WO1991019828A1 (en) * | 1990-06-19 | 1991-12-26 | Henkel Corporation | Liquid composition and process for treating aluminium or tin cans to impart corrosion resistance and reduced friction coefficient |
JPH04187782A (ja) * | 1990-11-21 | 1992-07-06 | Nippon Parkerizing Co Ltd | ぶりきdi缶用表面処理液 |
JPH05163584A (ja) * | 1991-12-12 | 1993-06-29 | Nippon Parkerizing Co Ltd | ぶりきdi缶用表面処理液 |
US5498300A (en) * | 1992-12-09 | 1996-03-12 | Henkel Corporation | Composition and process for treating tinplate |
JP3256009B2 (ja) * | 1992-12-09 | 2002-02-12 | 日本パーカライジング株式会社 | ぶりき材表面処理液及び表面処理方法 |
US5603754A (en) * | 1993-07-05 | 1997-02-18 | Henkel Corporation | Composition and process for treating tinplate and aluminum |
US5562950A (en) * | 1994-03-24 | 1996-10-08 | Novamax Technologies, Inc. | Tin coating composition and method |
JP3366724B2 (ja) * | 1994-04-20 | 2003-01-14 | 日本ペイント株式会社 | 金属表面用化成処理水溶液 |
US5965205A (en) * | 1995-07-21 | 1999-10-12 | Henkel Corporation | Composition and process for treating tinned surfaces |
US5711996A (en) * | 1995-09-28 | 1998-01-27 | Man-Gill Chemical Company | Aqueous coating compositions and coated metal surfaces |
AU5087798A (en) * | 1996-11-06 | 1998-05-29 | Henkel Corporation | Phosphate conversion coating composition and process |
JPH11128830A (ja) * | 1997-10-30 | 1999-05-18 | Nkk Corp | 耐食性に優れた表面処理鋼板 |
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DE3408577A1 (de) * | 1984-03-09 | 1985-09-12 | Metallgesellschaft Ag, 6000 Frankfurt | Verfahren zur phosphatierung von metallen |
-
1987
- 1987-10-13 JP JP62257678A patent/JPH01100281A/ja active Granted
-
1988
- 1988-10-11 DE DE3834480A patent/DE3834480A1/de not_active Withdrawn
- 1988-10-12 CA CA000579848A patent/CA1321859C/en not_active Expired - Fee Related
- 1988-10-13 GB GB8824016A patent/GB2210900B/en not_active Expired - Fee Related
- 1988-10-13 BR BR8805286A patent/BR8805286A/pt not_active IP Right Cessation
- 1988-10-13 AU AU23715/88A patent/AU608374B2/en not_active Ceased
- 1988-10-13 MX MX013399A patent/MX169760B/es unknown
- 1988-10-13 ZA ZA887663A patent/ZA887663B/xx unknown
- 1988-10-13 EP EP88202291A patent/EP0312176B1/de not_active Expired - Lifetime
- 1988-10-13 DE DE8888202291T patent/DE3876744D1/de not_active Expired - Fee Related
- 1988-10-13 US US07/256,935 patent/US4927472A/en not_active Expired - Fee Related
Also Published As
Publication number | Publication date |
---|---|
AU608374B2 (en) | 1991-03-28 |
EP0312176A1 (de) | 1989-04-19 |
US4927472A (en) | 1990-05-22 |
GB2210900A (en) | 1989-06-21 |
MX169760B (es) | 1993-07-23 |
CA1321859C (en) | 1993-09-07 |
BR8805286A (pt) | 1989-05-30 |
DE3834480A1 (de) | 1989-04-27 |
AU2371588A (en) | 1989-04-20 |
DE3876744D1 (de) | 1993-01-28 |
JPH0577750B2 (pt) | 1993-10-27 |
GB2210900B (en) | 1991-11-20 |
ZA887663B (en) | 1989-06-28 |
JPH01100281A (ja) | 1989-04-18 |
GB8824016D0 (en) | 1988-11-23 |
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