EP2092090B1 - Solution de phosphatage à base de zr/ti utilisée pour passiver des surfaces composites métalliques - Google Patents
Solution de phosphatage à base de zr/ti utilisée pour passiver des surfaces composites métalliques Download PDFInfo
- Publication number
- EP2092090B1 EP2092090B1 EP07820181A EP07820181A EP2092090B1 EP 2092090 B1 EP2092090 B1 EP 2092090B1 EP 07820181 A EP07820181 A EP 07820181A EP 07820181 A EP07820181 A EP 07820181A EP 2092090 B1 EP2092090 B1 EP 2092090B1
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- EP
- European Patent Office
- Prior art keywords
- zirconium
- steel
- ions
- ppm
- aqueous composition
- Prior art date
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- 238000002161 passivation Methods 0.000 title description 20
- 239000002905 metal composite material Substances 0.000 title 1
- 239000010936 titanium Substances 0.000 claims description 57
- 229910052782 aluminium Inorganic materials 0.000 claims description 54
- 238000000034 method Methods 0.000 claims description 54
- QCWXUUIWCKQGHC-UHFFFAOYSA-N Zirconium Chemical compound [Zr] QCWXUUIWCKQGHC-UHFFFAOYSA-N 0.000 claims description 53
- 229910052726 zirconium Inorganic materials 0.000 claims description 53
- XAGFODPZIPBFFR-UHFFFAOYSA-N aluminium Chemical compound [Al] XAGFODPZIPBFFR-UHFFFAOYSA-N 0.000 claims description 48
- 238000006243 chemical reaction Methods 0.000 claims description 46
- KRHYYFGTRYWZRS-UHFFFAOYSA-M Fluoride anion Chemical compound [F-] KRHYYFGTRYWZRS-UHFFFAOYSA-M 0.000 claims description 44
- 239000000203 mixture Substances 0.000 claims description 43
- 229910000831 Steel Inorganic materials 0.000 claims description 36
- 239000010959 steel Substances 0.000 claims description 36
- RTAQQCXQSZGOHL-UHFFFAOYSA-N Titanium Chemical compound [Ti] RTAQQCXQSZGOHL-UHFFFAOYSA-N 0.000 claims description 35
- NBIIXXVUZAFLBC-UHFFFAOYSA-K phosphate Chemical compound [O-]P([O-])([O-])=O NBIIXXVUZAFLBC-UHFFFAOYSA-K 0.000 claims description 32
- 229910052719 titanium Inorganic materials 0.000 claims description 28
- 229910019142 PO4 Inorganic materials 0.000 claims description 25
- 239000010452 phosphate Substances 0.000 claims description 25
- -1 zinc(II) ions Chemical class 0.000 claims description 24
- 239000002253 acid Substances 0.000 claims description 17
- 239000002131 composite material Substances 0.000 claims description 16
- 230000002829 reductive effect Effects 0.000 claims description 11
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 claims description 11
- 150000001875 compounds Chemical class 0.000 claims description 9
- 239000007769 metal material Substances 0.000 claims description 7
- 238000010276 construction Methods 0.000 claims description 5
- 238000004519 manufacturing process Methods 0.000 claims description 5
- JPVYNHNXODAKFH-UHFFFAOYSA-N Cu2+ Chemical compound [Cu+2] JPVYNHNXODAKFH-UHFFFAOYSA-N 0.000 claims description 4
- MHAJPDPJQMAIIY-UHFFFAOYSA-N Hydrogen peroxide Chemical compound OO MHAJPDPJQMAIIY-UHFFFAOYSA-N 0.000 claims description 4
- VEQPNABPJHWNSG-UHFFFAOYSA-N Nickel(2+) Chemical compound [Ni+2] VEQPNABPJHWNSG-UHFFFAOYSA-N 0.000 claims description 3
- 150000001768 cations Chemical class 0.000 claims description 3
- XTEGARKTQYYJKE-UHFFFAOYSA-M chlorate Inorganic materials [O-]Cl(=O)=O XTEGARKTQYYJKE-UHFFFAOYSA-M 0.000 claims description 3
- 125000001153 fluoro group Chemical group F* 0.000 claims description 3
- IDCPFAYURAQKDZ-UHFFFAOYSA-N 1-nitroguanidine Chemical compound NC(=N)N[N+]([O-])=O IDCPFAYURAQKDZ-UHFFFAOYSA-N 0.000 claims description 2
- BTJIUGUIPKRLHP-UHFFFAOYSA-N 4-nitrophenol Chemical compound OC1=CC=C([N+]([O-])=O)C=C1 BTJIUGUIPKRLHP-UHFFFAOYSA-N 0.000 claims description 2
- CWYNVVGOOAEACU-UHFFFAOYSA-N Fe2+ Chemical compound [Fe+2] CWYNVVGOOAEACU-UHFFFAOYSA-N 0.000 claims description 2
- AVXURJPOCDRRFD-UHFFFAOYSA-N Hydroxylamine Chemical compound ON AVXURJPOCDRRFD-UHFFFAOYSA-N 0.000 claims description 2
- HBBGRARXTFLTSG-UHFFFAOYSA-N Lithium ion Chemical compound [Li+] HBBGRARXTFLTSG-UHFFFAOYSA-N 0.000 claims description 2
- JLVVSXFLKOJNIY-UHFFFAOYSA-N Magnesium ion Chemical compound [Mg+2] JLVVSXFLKOJNIY-UHFFFAOYSA-N 0.000 claims description 2
- WAEMQWOKJMHJLA-UHFFFAOYSA-N Manganese(2+) Chemical compound [Mn+2] WAEMQWOKJMHJLA-UHFFFAOYSA-N 0.000 claims description 2
- XLJKHNWPARRRJB-UHFFFAOYSA-N cobalt(2+) Chemical compound [Co+2] XLJKHNWPARRRJB-UHFFFAOYSA-N 0.000 claims description 2
- 238000003618 dip coating Methods 0.000 claims description 2
- 235000000346 sugar Nutrition 0.000 claims description 2
- 239000004411 aluminium Substances 0.000 claims 5
- BHPQYMZQTOCNFJ-UHFFFAOYSA-N Calcium cation Chemical compound [Ca+2] BHPQYMZQTOCNFJ-UHFFFAOYSA-N 0.000 claims 1
- LFTLOKWAGJYHHR-UHFFFAOYSA-N N-methylmorpholine N-oxide Chemical compound CN1(=O)CCOCC1 LFTLOKWAGJYHHR-UHFFFAOYSA-N 0.000 claims 1
- WUKWITHWXAAZEY-UHFFFAOYSA-L calcium difluoride Chemical compound [F-].[F-].[Ca+2] WUKWITHWXAAZEY-UHFFFAOYSA-L 0.000 claims 1
- 239000010436 fluorite Substances 0.000 claims 1
- FZFRVZDLZISPFJ-UHFFFAOYSA-N tungsten(6+) Chemical compound [W+6] FZFRVZDLZISPFJ-UHFFFAOYSA-N 0.000 claims 1
- 239000000243 solution Substances 0.000 description 31
- 230000008569 process Effects 0.000 description 30
- 229910001335 Galvanized steel Inorganic materials 0.000 description 20
- 239000008397 galvanized steel Substances 0.000 description 20
- 239000000306 component Substances 0.000 description 16
- HCHKCACWOHOZIP-UHFFFAOYSA-N Zinc Chemical compound [Zn] HCHKCACWOHOZIP-UHFFFAOYSA-N 0.000 description 15
- 230000015572 biosynthetic process Effects 0.000 description 15
- 229910052751 metal Inorganic materials 0.000 description 15
- 239000002184 metal Substances 0.000 description 15
- 238000005554 pickling Methods 0.000 description 15
- 239000011701 zinc Substances 0.000 description 14
- 238000000576 coating method Methods 0.000 description 13
- 230000003287 optical effect Effects 0.000 description 13
- 229910052725 zinc Inorganic materials 0.000 description 13
- 239000011248 coating agent Substances 0.000 description 12
- 239000003973 paint Substances 0.000 description 10
- HEMHJVSKTPXQMS-UHFFFAOYSA-M Sodium hydroxide Chemical compound [OH-].[Na+] HEMHJVSKTPXQMS-UHFFFAOYSA-M 0.000 description 9
- 229910045601 alloy Inorganic materials 0.000 description 8
- 239000000956 alloy Substances 0.000 description 8
- 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 8
- 229910000165 zinc phosphate Inorganic materials 0.000 description 8
- 239000013078 crystal Substances 0.000 description 7
- 239000000758 substrate Substances 0.000 description 7
- 239000011521 glass Substances 0.000 description 6
- 230000007797 corrosion Effects 0.000 description 5
- 238000005260 corrosion Methods 0.000 description 5
- 238000000151 deposition Methods 0.000 description 5
- 230000008021 deposition Effects 0.000 description 5
- 239000000463 material Substances 0.000 description 5
- XEEYBQQBJWHFJM-UHFFFAOYSA-N Iron Chemical compound [Fe] XEEYBQQBJWHFJM-UHFFFAOYSA-N 0.000 description 4
- 238000011156 evaluation Methods 0.000 description 4
- 150000003609 titanium compounds Chemical class 0.000 description 4
- PXHVJJICTQNCMI-UHFFFAOYSA-N Nickel Chemical compound [Ni] PXHVJJICTQNCMI-UHFFFAOYSA-N 0.000 description 3
- PTFCDOFLOPIGGS-UHFFFAOYSA-N Zinc dication Chemical compound [Zn+2] PTFCDOFLOPIGGS-UHFFFAOYSA-N 0.000 description 3
- 239000010960 cold rolled steel Substances 0.000 description 3
- 230000000875 corresponding effect Effects 0.000 description 3
- 238000006073 displacement reaction Methods 0.000 description 3
- 229910052739 hydrogen Inorganic materials 0.000 description 3
- 239000001257 hydrogen Substances 0.000 description 3
- 150000003839 salts Chemical class 0.000 description 3
- 239000010802 sludge Substances 0.000 description 3
- 230000000007 visual effect Effects 0.000 description 3
- 238000005303 weighing Methods 0.000 description 3
- 229910003899 H2ZrF6 Inorganic materials 0.000 description 2
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 description 2
- 229910020491 K2TiF6 Inorganic materials 0.000 description 2
- 230000008901 benefit Effects 0.000 description 2
- 238000004140 cleaning Methods 0.000 description 2
- 238000007598 dipping method Methods 0.000 description 2
- 238000001035 drying Methods 0.000 description 2
- 238000004070 electrodeposition Methods 0.000 description 2
- 150000002222 fluorine compounds Chemical class 0.000 description 2
- 229910052742 iron Inorganic materials 0.000 description 2
- 239000004922 lacquer Substances 0.000 description 2
- 239000011572 manganese Substances 0.000 description 2
- 150000002739 metals Chemical class 0.000 description 2
- 229910052845 zircon Inorganic materials 0.000 description 2
- 150000003755 zirconium compounds Chemical class 0.000 description 2
- GFQYVLUOOAAOGM-UHFFFAOYSA-N zirconium(iv) silicate Chemical compound [Zr+4].[O-][Si]([O-])([O-])[O-] GFQYVLUOOAAOGM-UHFFFAOYSA-N 0.000 description 2
- OYPRJOBELJOOCE-UHFFFAOYSA-N Calcium Chemical compound [Ca] OYPRJOBELJOOCE-UHFFFAOYSA-N 0.000 description 1
- VYZAMTAEIAYCRO-UHFFFAOYSA-N Chromium Chemical compound [Cr] VYZAMTAEIAYCRO-UHFFFAOYSA-N 0.000 description 1
- RYGMFSIKBFXOCR-UHFFFAOYSA-N Copper Chemical compound [Cu] RYGMFSIKBFXOCR-UHFFFAOYSA-N 0.000 description 1
- 101100117236 Drosophila melanogaster speck gene Proteins 0.000 description 1
- FYYHWMGAXLPEAU-UHFFFAOYSA-N Magnesium Chemical compound [Mg] FYYHWMGAXLPEAU-UHFFFAOYSA-N 0.000 description 1
- PWHULOQIROXLJO-UHFFFAOYSA-N Manganese Chemical compound [Mn] PWHULOQIROXLJO-UHFFFAOYSA-N 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
- XUIMIQQOPSSXEZ-UHFFFAOYSA-N Silicon Chemical compound [Si] XUIMIQQOPSSXEZ-UHFFFAOYSA-N 0.000 description 1
- FAPWRFPIFSIZLT-UHFFFAOYSA-M Sodium chloride Chemical compound [Na+].[Cl-] FAPWRFPIFSIZLT-UHFFFAOYSA-M 0.000 description 1
- 238000009825 accumulation Methods 0.000 description 1
- 230000003213 activating effect Effects 0.000 description 1
- 239000000654 additive Substances 0.000 description 1
- 230000002411 adverse Effects 0.000 description 1
- 238000007605 air drying Methods 0.000 description 1
- 238000005275 alloying Methods 0.000 description 1
- 150000004645 aluminates Chemical class 0.000 description 1
- 238000013459 approach Methods 0.000 description 1
- 230000004888 barrier function Effects 0.000 description 1
- 230000003139 buffering effect Effects 0.000 description 1
- 229910052791 calcium Inorganic materials 0.000 description 1
- 239000011575 calcium Substances 0.000 description 1
- 239000012482 calibration solution Substances 0.000 description 1
- 230000008859 change Effects 0.000 description 1
- 239000007795 chemical reaction product Substances 0.000 description 1
- 239000003795 chemical substances by application Substances 0.000 description 1
- 229910052804 chromium Inorganic materials 0.000 description 1
- 239000011651 chromium Substances 0.000 description 1
- 230000000536 complexating effect Effects 0.000 description 1
- 229910052802 copper Inorganic materials 0.000 description 1
- 239000010949 copper Substances 0.000 description 1
- 230000002596 correlated effect Effects 0.000 description 1
- 229910001610 cryolite Inorganic materials 0.000 description 1
- 230000003247 decreasing effect Effects 0.000 description 1
- 230000007547 defect Effects 0.000 description 1
- 238000005238 degreasing Methods 0.000 description 1
- 230000006866 deterioration Effects 0.000 description 1
- 238000011161 development Methods 0.000 description 1
- 238000007865 diluting Methods 0.000 description 1
- 230000000694 effects Effects 0.000 description 1
- 238000000635 electron micrograph Methods 0.000 description 1
- 238000002474 experimental method Methods 0.000 description 1
- 238000011010 flushing procedure Methods 0.000 description 1
- 150000002431 hydrogen Chemical class 0.000 description 1
- 238000011835 investigation Methods 0.000 description 1
- 150000002500 ions Chemical class 0.000 description 1
- 239000011777 magnesium Substances 0.000 description 1
- 229910052749 magnesium Inorganic materials 0.000 description 1
- 238000012423 maintenance Methods 0.000 description 1
- 229910001437 manganese ion Inorganic materials 0.000 description 1
- WPBNNNQJVZRUHP-UHFFFAOYSA-L manganese(2+);methyl n-[[2-(methoxycarbonylcarbamothioylamino)phenyl]carbamothioyl]carbamate;n-[2-(sulfidocarbothioylamino)ethyl]carbamodithioate Chemical compound [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
- 229910052759 nickel Inorganic materials 0.000 description 1
- 229910001453 nickel ion Inorganic materials 0.000 description 1
- 230000036961 partial effect Effects 0.000 description 1
- 239000002245 particle Substances 0.000 description 1
- 231100000614 poison Toxicity 0.000 description 1
- 230000007096 poisonous effect Effects 0.000 description 1
- 239000000047 product Substances 0.000 description 1
- 238000004064 recycling Methods 0.000 description 1
- 238000002310 reflectometry Methods 0.000 description 1
- 229910052710 silicon Inorganic materials 0.000 description 1
- 239000010703 silicon Substances 0.000 description 1
- 238000005507 spraying Methods 0.000 description 1
- 238000011272 standard treatment Methods 0.000 description 1
- 150000008163 sugars Chemical class 0.000 description 1
- 230000009897 systematic effect Effects 0.000 description 1
- 238000012360 testing method Methods 0.000 description 1
- PMTRSEDNJGMXLN-UHFFFAOYSA-N titanium zirconium Chemical compound [Ti].[Zr] PMTRSEDNJGMXLN-UHFFFAOYSA-N 0.000 description 1
- JUWGUJSXVOBPHP-UHFFFAOYSA-B titanium(4+);tetraphosphate Chemical compound [Ti+4].[Ti+4].[Ti+4].[O-]P([O-])([O-])=O.[O-]P([O-])([O-])=O.[O-]P([O-])([O-])=O.[O-]P([O-])([O-])=O JUWGUJSXVOBPHP-UHFFFAOYSA-B 0.000 description 1
- 230000007704 transition Effects 0.000 description 1
- WFKWXMTUELFFGS-UHFFFAOYSA-N tungsten Chemical compound [W] WFKWXMTUELFFGS-UHFFFAOYSA-N 0.000 description 1
- 229910052721 tungsten Inorganic materials 0.000 description 1
- 239000010937 tungsten Substances 0.000 description 1
- 239000013585 weight reducing agent Substances 0.000 description 1
- 238000010626 work up procedure Methods 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
- C23C22/12—Orthophosphates containing zinc cations
-
- 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
- C23C22/34—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 fluorides or complex fluorides
- C23C22/36—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 fluorides or complex fluorides containing also phosphates
- C23C22/364—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 fluorides or complex fluorides containing also phosphates containing also manganese cations
- C23C22/365—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 fluorides or complex fluorides containing also phosphates containing also manganese cations containing also zinc and nickel cations
-
- 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
- C23C22/78—Pretreatment of the material to be coated
-
- 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
- C23G1/14—Cleaning or pickling metallic material with solutions or molten salts with alkaline solutions
-
- Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y10—TECHNICAL SUBJECTS COVERED BY FORMER USPC
- Y10T—TECHNICAL SUBJECTS COVERED BY FORMER US CLASSIFICATION
- Y10T428/00—Stock material or miscellaneous articles
- Y10T428/12—All metal or with adjacent metals
- Y10T428/12493—Composite; i.e., plural, adjacent, spatially distinct metal components [e.g., layers, joint, etc.]
- Y10T428/12736—Al-base component
- Y10T428/1275—Next to Group VIII or IB metal-base component
- Y10T428/12757—Fe
Definitions
- the present invention relates to an aqueous composition and a process for the corrosion-protective conversion treatment of metallic surfaces.
- the aqueous composition is particularly suitable for treating various metallic materials joined together in composite structures, including steel or galvanized or alloy galvanized steel, and any combination of these materials, which composite structure is at least partially composed of aluminum or its alloys.
- alloys are always included that consist of more than 50 atomic% of aluminum.
- the metallic surfaces of the composite structure treated according to the invention can be coated homogeneously and with outstanding adhesion properties in a subsequent dip coating, so that post-passivation of the conversion-treated metallic surfaces can be dispensed with.
- the clear advantage of the aqueous composition according to the invention for the treatment of metallic surfaces consists in the selective coating of different metal surfaces with a crystalline phosphate layer in the case of steel or galvanized or alloy galvanized steel surfaces and a non-crystalline conversion layer on the aluminum surfaces such that an excellent passivation of the metallic surfaces and a sufficient paint adhesion for subsequently applied paint results.
- the application of the aqueous composition according to the invention therefore enables a one-step process for the anticorrosive pretreatment of composite metal structures.
- the accumulation of aluminum ions in the bath solution leads to a significant deterioration of the phosphating process, in particular the quality of the conversion layer.
- the formation of a homogeneous crystalline phosphate layer on steel surfaces does not occur in the presence of trivalent cations of aluminum.
- Aluminum ions therefore act as a poisonous agent in phosphating and must be effectively masked by suitable additives in the case of standard treatment of bodies which have partially aluminum surfaces.
- a suitable masking of the aluminum ions may be via the addition of fluoride ions or fluoro complexes such as SiF 6 2- , as in US 5,683,357 disclosed to be achieved.
- hexafluoroaluminates for example in the form of cryolite, can be precipitated from the bath solution, which contribute to a considerable extent to the formation of sludge in the phosphating bath and thus considerably complicate the processability of the phosphating.
- the formation of a phosphate layer on the aluminum surface takes place only at high pickling rates, ie a relatively high concentration of free fluoride ions.
- the control of defined bath parameters, in particular the free fluoride content is of considerable importance for a sufficient corrosion protection and a good paint adhesion. Insufficient phosphating of the aluminum surfaces always requires post-passivation in a subsequent process step.
- optical defects after the coating primer caused by an inhomogeneously deposited phosphate layer are basically not curable.
- DE10322446 uses conventional phosphating and adds water-soluble zirconium and / or titanium compounds, with a certain amount, but not more than 5000 ppm, of free fluoride.
- phosphating solutions in which the total content of zirconium and / or titanium is in a range from 10 to 1000 ppm, preferably 50 to 250 ppm, can be dispensed with after passivation of both the phosphated metal surfaces and the aluminum surfaces.
- the single-stage process of a conversion treatment of metallic surfaces which at least partially comprise aluminum surfaces is carried out with constantly high fluoride contents, which causes a high pickling rate and thus a massive introduction of aluminum ions into the bath solution. It is the associated technical effort in bath control and treatment, which inevitably results from increased sludge formation in the phosphating. Furthermore, sedimented aluminate particles can remain on the components which have undergone such a conversion, which after the deposition of the coating primer cause a negative visual impression of the painted components or impair the paint adhesion and mechanical resistance of the paint.
- the DE10231279 relates to a process for the corrosion-protective pretreatment of metal surfaces, which consist of at least 5% of aluminum surfaces and in addition to these aluminum surfaces predominantly surfaces of iron and / or zinc.
- the DE10231279 teaches therefore a method for corrosion-protective treatment of metals in mixed construction. According to the process described there, crystalline coatings are to be produced on all metal surfaces.
- the corrosion protection pretreatment after the DE10231279 is made by means of a composition suitable for zinc phosphating, said composition having in addition to 0.2-4 g / l of zinc ions and 4-65 g / l of phosphate ions a free fluoride content in the range of about 30-500 ppm , preferably in the range of 85-350 ppm.
- the DE10231279 discloses that the composition contains an additional amount of dissolved titanium or zirconium in the Range of 1-200 ppm, wherein the proportion of these elements in the composition is preferably zero.
- the WO 02/070782 A2 relates to a method for nickel-free phosphating of metal surfaces by contacting with phosphating, which can contain in addition to zinc and phosphate ions also a proportion of free fluoride and complex fluorides based on the elements zirconium and / or titanium.
- the proportion of free fluoride in the phosphating solution is preferably in the range of about 1-800 ppm.
- the proportion of complex fluorides of zirconium and / or titanium in the phosphating solution is preferably in the range of about 3-300 ppm based on F6.
- the WO 02/070782 A2 further teaches that for the treatment of aluminum surfaces, a value of about 50 ppm relative to F6 should not be exceeded. That in the WO 02/070782 A2
- the process disclosed is particularly suitable for zinc surfaces, but can also be used for metal surfaces consisting of at least one of the materials based on aluminum, iron, steel and zinc.
- F / mM and Me / mM represent the free fluoride (F) or reduced zirconium and / or titanium concentration (Me) reduced by the unit of concentration in mM (10 -3 mol / L).
- the quotient ⁇ is at least 4.
- Ratio ⁇ for aqueous compositions which according to the invention contain both components (c), ie zirconium and titanium compounds, is the Ratio ⁇ according to formula (I) should not be less than Zr / mM Zr / mM + Ti / mM ⁇ 4 + Ti / mM Zr / mM + Ti / mM ⁇ 6
- the proportion of free fluoride in such an aqueous composition is determined potentiometrically with the aid of a fluoride-sensitive glass electrode.
- a detailed description of the measuring method, the calibration and the experimental procedure for determining the free fluoride concentration can be found in the description of the embodiments of the present invention.
- zirconium compounds provides technically better results than the use of titanium compounds in the different embodiments of the present invention.
- complex fluoro acids or their salts can be used.
- the aqueous composition in the process according to the invention for corrosion-protective conversion treatment can be used in addition to 0.3 to 3 g / l Zn (II) and 5 to 40 g / l Phosphate ions as well 1 to 200 ppm one or more water-soluble compounds of zirconium and / or titanium based on the element zirconium and / or titanium also contain at least one of the following accelerators: 0.3 to 4 g / l chlorate, 0.01 to 0.2 g / l Nitrite ions, 0.05 to 4 g / l nitroguanidine, 0.05 to 4 g / l N-methyl-N-oxide, 0.2 to 2 g / l m-nitrobenzenesulfonate ions, 0.05 to 2 g / l m-nitrobenzoate ions, 0.05 to 2 g / l p-nitrophenol, 1 to 150 mg / l Hydrogen peroxide in free or bound form,
- Such accelerators are known in the art as components of Phosphatierbädem and fulfill the role of "hydrogen scavengers" by these by the Acid attack on the metallic surface resulting hydrogen directly oxidize and thereby be reduced.
- the formation of a homogeneous crystalline zinc phosphate layer is greatly facilitated by the accelerator, which reduces the formation of gaseous hydrogen on the metal surface.
- Corrosion protection and lacquer adhesion of the crystalline zinc phosphate layers produced with an aqueous composition in the process according to the invention are, according to experience, improved if one or more of the following cations is additionally present: 0.001 to 4 g / l Manganese (II), 0.001 to 4 g / l Nickel (II), 0.001 to 4 g / l Cobalt (II) 0.002 to 0.2 g / l Copper (II), 0.2 to 2.5 g / l Magnesium (II) 0.2 to 2.5 g / l Calcium (II), 0.01 to 0.5 g / l Iron (II), 0.2 to 1.5 g / l Lithium (I), 0.02 to 0.8 g / l Tungsten (VI).
- the zinc concentration is preferably in the range between about 0.3 and about 2 g / l, and more preferably between about 0.8 and about 1.4 g / l.
- Higher levels of zinc do not provide significant benefits to the conversion treatment of the invention with the aqueous composition, but on the other hand cause increased sludge build up in the treatment bath.
- high levels of zinc can occur in a working treatment bath when mainly galvanized surfaces are phosphated and thus additional zinc is introduced into the treatment bath as a result of the pickling process.
- Aqueous conversion conversion compositions containing both manganese and nickel ions in addition to zinc ions are well known to those skilled in phosphating as trication-phosphating solutions and are also useful in the present invention suitable.
- usual share of up to 3 g / l nitrate facilitates the formation of a crystalline homogeneous and closed phosphate layer on the steel, galvanized and alloy-galvanized steel surfaces.
- hexafluorosilicate anions can be added to the aqueous composition for the anticorrosive conversion treatment according to the invention, since these are capable of complexing the trivalent aluminum cations introduced into the bath solution, so that the phosphating is optimized and the so-called "speck formation” occurs under the formation of specks on the surface increased pickling rate associated with the deposition of amorphous, white zinc phosphate, is prevented on galvanized substrates.
- the aqueous treatment solution preferably has a free acid content, each staggered in accordance with an increasing preference, of at least 0; 0.2; 0.5; 0.8; 1 point but not more than 3; 2.5; 2; 1.5 points.
- a total acid content of the treatment solution each staggered according to an increasing preference, of at least 20; 21; 22 points but not more than 26; 25; 24 points available.
- the term free acid is well known to those skilled in the phosphating art.
- the method of determination specific for this invention for determining the free acid or the total acid content is given in the examples section.
- the pH of the aqueous treatment solution is preferably not less than 2.2 with increasing preference. 2.4; 2.6; 2.8 but not greater than 3.6; 3.5; 3.4; 3.3; 3.2.
- aqueous composition for the conversion treatment according to the invention composed of metallic materials composite structures, which at least partially also aluminum surfaces, takes place after cleaning and degreasing of the surfaces by bringing the surfaces in contact the aqueous composition according to the invention, for example by spraying or dipping, at bath temperatures in the range of 20-65 ° C for a time interval tuned to the convection in the bath and for the composition of the composite structure to be treated.
- a dipping process is usually followed by a rinse with city water or demineralized water, after work-up of enriched with components of the treatment solution rinse water, a partial recycling of rinse water components can be made in the bath solution.
- the thus treated metallic surfaces of the composite structure can be provided with a base coat in a further step, preferably with an organic electrodeposition paint.
- a post-passivation of the phosphated and / or passivated metal surfaces with an aqueous composition can take place, which is at least 200 contains up to 1500 ppm of fluorocomplexes of zirconium and / or titanium based on the elements zirconium and / or titanium and optionally 10 to 100 ppm of copper (II) ions.
- the pH of such a post-passivation solution is in the range of 3.5 to 5.5.
- a composite structure treated in accordance with the method according to the invention composed inter alia of steel and / or galvanized and / or alloy-galvanized steel components and aluminum components, has coating weights of phosphating of 0.5 to 4.5 g on its metallic surfaces on which a crystalline zinc phosphate layer has been formed / m 2 on.
- the metallic surfaces which can be treated with the aqueous composition according to the method for forming a conversion layer are preferably steel, galvanized steel and alloy galvanized steel, and aluminum and alloys of aluminum having an alloying content of less than 50 at% Alloy components silicon, magnesium, copper, manganese, Zinc, chromium, titanium and nickel come into question.
- the metallic surface may be composed of any combination of said materials in a composite structure.
- the converted in accordance with the underlying invention metallic materials, components and composite structures are used in automotive production in the body shop, shipbuilding, construction and for the production of white goods use.
- Table 1 shows the sequence of processes for the inventive treatment of the sample sheets, as is in principle also customary in automotive bodywork.
- the sheets are alkaline cleaned and degreased and prepared after a rinsing with a titanium phosphate-containing activating solution for the conversion treatment according to the invention.
- commercially available products by the applicant were used: Ridoline® ® 1569 A, Ridosol ® 1270, FIXODINE ® 50 CF.
- the free acid score is determined by diluting 10 ml bath sample to 50 ml and titrating to pH 3.6 with 0.1 N sodium hydroxide solution. The consumption of ml of sodium hydroxide gives the score. Accordingly, the content of total acid is determined by titrating to a pH of 8.5.
- the content of free fluoride in the aqueous composition for the conversion treatment is detected by means of a potentiometric measuring chain (inoLab pH / Ion Level 3, from WTW).
- the measuring chain contains a fluoride-sensitive glass electrode (F501, Fa. WTW) and a reference electrode (R503, Fa. WTW).
- F501, Fa. WTW fluoride-sensitive glass electrode
- R503, Fa. WTW reference electrode
- For two-point calibration of both electrodes are immersed together in sequence in the calibration solutions with a content of 100 ppm and 1000 ppm prepared from the Titrisol ® fluoride standard of Fa. Merck without buffer addition.
- the resulting measured values are correlated with the respective fluoride content "100" or "1000" and read into the measuring instrument.
- the steepness of the glass electrode is then displayed in mV per decade of the fluoride ion content in ppm on the meter, typically between -55 and -60 mV.
- the fluoride content in ppm can then be determined directly by immersing the two electrodes in the cooled bath solution for conversion treatment.
- Table 1 Process for Conversion Treatment of Aluminum (AC 120), CRS ST1405 (Sidca) and HDG (Thyssen) steps 1. alkaline cleaning 2nd flushing process 3. Activate 4. phosphating 5. rinsing process 6.
- Table 2 shows the pickling rates for the substrate aluminum as a function of the concentration of free fluoride and zirconium for a process sequence according to Table 1. As expected, the pickling rate increases with each increase in fluoride concentration. Surprisingly, the pickling rate on aluminum is significantly reduced by the addition of 50 ppm, and in the case of a free fluoride concentration of 30 and 55 ppm, the pickling rate is reduced by 50% compared with an aqueous composition for conversion treatment containing no zirconium.
- Tables 8 to 10 contain, depending on the quotient ⁇ of the respectively used treatment solutions a) to c) an optical assessment of phosphating on cold-rolled steel, since the formation of a closed and homogeneous zinc phosphate layer is critical especially on this substrate.
- the sample sheet is subdivided into a line grid in such a way that an optical individual evaluation of approximately 1 cm 2 square fields is made.
- the mean value of the covering degrees summed over all individual fields then yields, semi-quantitatively, the total coverage of the respective sheet with the phosphate layer as a percentage of the sheet metal surface examined, whereby this consists of at least 64 individual fields. Coated and uncoated areas are distinguishable for the skilled person due to their different reflectivity and / or color.
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Claims (13)
- Procédé pour le traitement de conversion anticorrosion de structures composites assemblées à partir de matériaux métalliques qui comprennent, à côté de surfaces d'acier et/ou d'acier zingué et/ou d'acier allié galvanisé, également des surfaces d'aluminium, caractérisé en ce que les surfaces métalliques nettoyées et sont mises en contact avec une composition aqueuse comprenant :(a) de 5 à 50 g/l d'ions de phosphate ;(b) de 0,3 à 3 g/l d'ions de zinc(II) ;(c) un total de 1 à 200 ppm d'un ou de plusieurs composés de zirconium ou de zirconium et de titane solubles dans l'eau, rapportées à l'élément zirconium ou aux éléments zirconium et titane ;(d) une quantité de fluorure libre de 1 à 400 ppm, mesurée avec une électrode sensible au fluorure ;caractérisé en ce que
le quotient λ répondant à la formule (I)
dans laquelle F / mM et Me / mM représentent la concentration de fluorure libre (F), respectivement la concentration de zirconium et/ou de titane (Me) réduites à l'unité de concentration en mM, s'élève à au moins - Procédé selon la revendication 1 , caractérisé en ce que le quotient λ répondant à la formule (I) pour des compositions aqueuses qui contiennent à titre de composant (c) exclusivement des composés de zirconium solubles dans l'eau, s'élève à au moins 4,5, de préférence à au moins 5, mais n'est pas supérieur à 8.
- Procédé selon l'une quelconque des revendications 1 à 2, caractérisé en ce que la composition aqueuse contient en outre au moins une des quantités suivantes des accélérateurs mentionnés ci-après:
de 0,3 à 4 g/l d'ions de chlorate; de 0,01 à 0,2 g/l d'ions de nitrite ; de 0,05 à 4 g/l de nitroguanidine ; de 0,05 à 4 g/l de N-oxyde de N-méthylmorpholine ; de 0,2 à 2 g/l d'ions de m-nitrobenzènesulfonate ; de 0,05 à 2 g/l d'ions de m-nitrobenzoate ; de 0,05 à 2 g/l de p-nitrophénol ; de 1 à 150 mg/l de peroxyde d'hydrogène sous forme libre ou liée; de 0,1 à 10 g/l d'hydroxylamine sous forme libre ou liée; de 0,1 à 10 g/l d'un sucre réducteur. - Procédé selon l'une quelconque des revendications 1 à 3, caractérisé en ce que la composition aqueuse contient en outre une ou plusieurs des quantités de cations mentionnées ci-après :de 0,001 à 4 g/l de manganèse(II) ;de 0,001 à 4 g/l de nickel(II) ;de 0,001 à 4 g/l de cobalt(II) ;de 0,002 à 0,2 g/l de cuivre(II) ;de 0,2 à 2,5 g/l de magnésium(II) ;de 0,2 à 2,5 g/l de calcium(II) ;de 0,01 à 0,5 g/l de fer(II) ;de 0,2 à 1,5g/l de lithium(I) ;de 0,02 à 0,8 g/l de tungstène(VI).
- Procédé selon l'une quelconque des revendications 1 à 4, caractérisé en ce que la composition aqueuse présente une teneur en acide libre de 0 peint, de préférence d'au moins 0,5 point, de manière particulièrement préférée d'au moins 1 joint, mais qui n'est pas supérieure à 3 points, de préférence pas supérieure à 2 points et de manière particulièrement préférée pas supérieure à 1,5 point, la teneur totale en acide s'élevant à au moins 20 points, de préférence à au moins 22 points, mais n'étant pas supérieure à 26 points, de préférence pas supérieure à 24 points.
- Procédé selon l'une quelconque des revendications 1 à 5, caractérisé en ce que la composition aqueuse présente une valeur de pH qui n'est pas inférieure à 2,2, de préférence qui n'est pas inférieure à et de manière particulièrement préférée qui n'est pas inférieure à 2,6, mais qui n'est pas supérieure à 3,8, de préférence pas supérieure à 3,6 et de manière particulièrement préférée pas supérieure à 3,2, une température dans la plage de 20 à 65 °C étant maintenue.
- Procédé selon une ou plusieurs des revendications précédentes, caractérisé en ce que les surfaces métalliques traitées de la sorte, dans lesquelles sont présentes une couche surfacique de phosphate cristallin, la couche recouvrant une surface de 0,5 à 4,5 g/m2, sur les surfaces d'acier, d'acier zingué et d'acier allié galvanisé, et une couche de conversion non cristalline sur les surfaces d'aluminium, sont enduites, dans une étape opératoire ultérieure, d'une laque d'électrodéposition, avec ou sans cycle de rinçage intermédiaire à l'eau.
- Procédé selon une ou plusieurs des revendications précédentes, caractérisé en ce que, après la mise en contact des surfaces métalliques avec la composition aqueuse, on ne procédé pas à un rinçage ultérieur de passivation.
- Procédé selon l'une quelconque des revendications 1 à 7, caractérisé en ce que, après la mise en contact des surfaces métalliques avec la composition aqueuse, on procède à un rinçage ultérieur de passivation avec ou sans cycle de rinçage intermédiaire à l'eau.
- Procédé selon la revendication 9, caractérisé en ce que le rinçage ultérieur de passivation présente une valeur de pH dans la plage de 3,5 à 5,5 et contient au total de 200 à 1500 ppm de fluorocomplexes de zirconium et/ou de titane, rapportées aux éléments zirconium et/ou titane, et le cas échéant de 10 à 100 ppm d'ions de cuivre(II).
- Élément métallique contenant des surfaces d'acier et/ou d'acier zingué et/ou d'acier allié galvanisé et au moins une surface d'aluminium, dans lequel, pour autant qu'elles soient présentes, aussi bien les surfaces d'acier que les surfaces d'acier zingué et d'acier allié galvanisé sont recouvertes d'une couche surfacique de phosphate cristallin, la couche recouvrant une surface de 0,5 à 4,5 g/m2, tandis que l'on réalise sur la surface d'aluminium une couche de conversion non cristalline, caractérisé en ce que l'élément métallique a été soumis à un prétraitement conformément à l'une quelconque des revendications 1 à 10.
- Utilisation d'un élément métallique selon la revendication 11, en carrosserie dans la fabrication automobile, dans la construction navale, dans l'industrie du bâtiment ainsi que pour la fabrication de produits blancs.
- Composition aqueuse pour le traitement de conversion anticorrosion de surfaces métalliques qui comprennent des surfaces d'acier ou d'acier zingué d'acier allié galvanisé ou d'aluminium ainsi que toutes les combinaisons desdites surfaces, qui contient :(a) de 5 à 50 g/l d'ions de phosphate;(b) de 0,3 à 3 g/l de zinc(II) ;(c) un total de 1 à 200 ppm de composés choisis parmi des composés de zirconium et de titane solubles dans l'eau, rapportées aux éléments zirconium et titane, la composition contenant à titre exclusif un ou plusieurs composés de zirconium soluble dans l'eau ;(d) une quantité de fluorure libre de 1 à 400 ppm, mesurée avec une électrode sensible au fluorure ;caractérisée en ce que
le quotient λ répondant à la formule (I)
dans laquelle F / mM et Me / mM représentent la concentration de fluorure libre (F), respectivement la concentration de zirconium et/ou de titane (Me) réduites à l'unité de concentration en mM, s'élève à au moins 4, mais n'est pas supérieur à 10.
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SI200731183T SI2092090T1 (sl) | 2006-11-08 | 2007-09-13 | Fosfatirna raztopina, ki vsebuje zr/ti za pasiviranje kovinskih kompozitnih povrĺ in |
PL07820181T PL2092090T3 (pl) | 2006-11-08 | 2007-09-13 | Zawierający Zr/Ti roztwór fosforanujący do pasywacji powierzchni metalicznych kompozytów |
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DE102006052919A DE102006052919A1 (de) | 2006-11-08 | 2006-11-08 | Zr-/Ti-haltige Phosphatierlösung zur Passivierung von Metallverbundoberflächen |
PCT/EP2007/059628 WO2008055726A1 (fr) | 2006-11-08 | 2007-09-13 | Solution de phosphatage à base de zr/ti utilisée pour passiver des surfaces composites métalliques |
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EP2092090A1 EP2092090A1 (fr) | 2009-08-26 |
EP2092090B1 true EP2092090B1 (fr) | 2012-12-19 |
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US (2) | US8801871B2 (fr) |
EP (1) | EP2092090B1 (fr) |
JP (1) | JP5406723B2 (fr) |
KR (1) | KR20090086405A (fr) |
CN (1) | CN101535528B (fr) |
BR (1) | BRPI0718578A2 (fr) |
CA (1) | CA2669042C (fr) |
DE (1) | DE102006052919A1 (fr) |
ES (1) | ES2398594T3 (fr) |
PL (1) | PL2092090T3 (fr) |
RU (1) | RU2464356C2 (fr) |
SI (1) | SI2092090T1 (fr) |
WO (1) | WO2008055726A1 (fr) |
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Cited By (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
EP2824213A1 (fr) | 2013-07-12 | 2015-01-14 | Voestalpine Stahl GmbH | Procédé d'amélioration de l'adhérence sur une tôle d'acier dotée d'un revêtement de protection |
Families Citing this family (19)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
CA2651393C (fr) | 2006-05-10 | 2016-11-01 | Henkel Ag & Co. Kgaa | Composition amelioree comprenant du chrome trivalent s'utilisant pour former des couches anti-corrosion sur des surfaces metalliques |
DE102008000600B4 (de) * | 2008-03-11 | 2010-05-12 | Chemetall Gmbh | Verfahren zur Beschichtung von metallischen Oberflächen mit einem Passivierungsmittel, das Passivierungsmittel, die hiermit erzeugte Beschichtung und ihre Verwendung |
JP5593532B2 (ja) * | 2008-07-30 | 2014-09-24 | ディップソール株式会社 | 亜鉛又は亜鉛合金めっき上にクロムフリー化成皮膜を形成するための化成処理水溶液及びそれより得られたクロムフリー化成皮膜 |
DE102009029334A1 (de) * | 2009-09-10 | 2011-03-24 | Henkel Ag & Co. Kgaa | Zweistufiges Verfahren zur korrosionsschützenden Behandlung von Metalloberflächen |
DE102009047523A1 (de) * | 2009-12-04 | 2011-06-09 | Henkel Ag & Co. Kgaa | Mehrstufiges Vorbehandlungsverfahren für metallische Bauteile mit Zinnoberflächen |
DE102009047522A1 (de) | 2009-12-04 | 2011-06-09 | Henkel Ag & Co. Kgaa | Mehrstufiges Vorbehandlungsverfahren für metallische Bauteile mit Zink- und Eisenoberflächen |
DE102010030697A1 (de) * | 2010-06-30 | 2012-01-05 | Henkel Ag & Co. Kgaa | Verfahren zur selektiven Phosphatierung einer Verbundmetallkonstruktion |
JP5861249B2 (ja) * | 2010-09-15 | 2016-02-16 | Jfeスチール株式会社 | 容器用鋼板の製造方法 |
WO2013033372A1 (fr) * | 2011-09-02 | 2013-03-07 | Ppg Industries Ohio, Inc. | Procédé de phosphatation au zinc en deux étapes |
EP2631333A1 (fr) * | 2012-02-24 | 2013-08-28 | Henkel AG & Co. KGaA | Prétraitement de surfaces en zinc avant une passivation |
GB2508827A (en) | 2012-12-11 | 2014-06-18 | Henkel Ag & Co Kgaa | Aqueous compositions and processes for passivating and brightening stainless steel surfaces |
US10156016B2 (en) | 2013-03-15 | 2018-12-18 | Henkel Ag & Co. Kgaa | Trivalent chromium-containing composition for aluminum and aluminum alloys |
EP2862957B1 (fr) | 2013-10-16 | 2019-08-07 | Coatings Foreign IP Co. LLC | Procédé de production de revêtement multicouche |
CZ305721B6 (cs) * | 2014-11-11 | 2016-02-17 | Univerzita J. E. Purkyně V Ústí Nad Labem | Způsob povlakování kovových forem ze slitin typu Al - Mg a Al - Si, zejména pro výrobu pneumatik motorových vozidel v automobilovém průmyslu |
US9631281B2 (en) * | 2014-12-04 | 2017-04-25 | Axalta Coating Systems Ip Co., Llc | Processes for producing a multilayer coating |
EP3502311A1 (fr) * | 2017-12-20 | 2019-06-26 | Henkel AG & Co. KGaA | Procédé de prétraitement de nettoyage et de protection anticorrosion de composants métalliques |
BR112020015010A2 (pt) | 2018-02-19 | 2021-01-19 | Chemetall Gmbh | Método para pré-tratamento químico e fosfatação seletiva, composição de fosfatação de zinco, concentrado, construção de metal compósito, e, uso da construção de metal compósito |
RU2690876C1 (ru) * | 2018-06-14 | 2019-06-06 | Закрытое Акционерное общество "ФК" (ЗАО " ФК") | Способ получения фосфатного покрытия |
CN111893467B (zh) * | 2020-07-30 | 2022-12-13 | 中铝材料应用研究院有限公司 | 一种改进的铝合金磷化工艺 |
Family Cites Families (17)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JP2695963B2 (ja) * | 1990-03-16 | 1998-01-14 | マツダ株式会社 | 金属表面のリン酸塩処理方法 |
JP2826242B2 (ja) * | 1992-11-30 | 1998-11-18 | 日本ペイント株式会社 | 金属表面のりん酸塩処理方法 |
CA2150545A1 (fr) * | 1992-12-22 | 1994-07-07 | Robert W. Miller | Composition et methode de revetement par conversion de phosphate pratiquement exempt de nickel |
JPH08246161A (ja) * | 1995-03-07 | 1996-09-24 | Mazda Motor Corp | 金属表面のリン酸塩処理方法 |
DE19511573A1 (de) * | 1995-03-29 | 1996-10-02 | Henkel Kgaa | Verfahren zur Phosphatierung mit metallhaltiger Nachspülung |
DE19606018A1 (de) * | 1996-02-19 | 1997-08-21 | Henkel Kgaa | Zinkphosphatierung mit geringen Gehalten an Nickel- und/oder Cobalt |
JPH09228066A (ja) * | 1996-02-27 | 1997-09-02 | Nippon Parkerizing Co Ltd | アルミニウム含有金属材料の耐食性・塑性加工性増進表面処理用水性組成物、処理液、および処理方法 |
JP3185966B2 (ja) | 1996-04-10 | 2001-07-11 | 日本ペイント株式会社 | 金属成型物のリン酸亜鉛皮膜処理方法 |
AU756876B2 (en) * | 1997-09-10 | 2003-01-23 | Henkel Kommanditgesellschaft Auf Aktien | Pretreatment before painting of composite metal structures containing aluminum portions |
MXPA03006677A (es) * | 2001-02-16 | 2003-10-24 | Henkel Kgaa | Proceso para tratar articulos de metales multiples. |
DE10110834B4 (de) * | 2001-03-06 | 2005-03-10 | Chemetall Gmbh | Verfahren zur Beschichtung von metallischen Oberflächen und Verwendung der derart beschichteten Substrate |
JP2003055796A (ja) * | 2001-08-09 | 2003-02-26 | Showa Denko Kk | アルミニウム材およびその製造方法、ならびに電子写真用感光体および電解コンデンサ電極用アルミニウム材料 |
DE10231279B3 (de) * | 2002-07-10 | 2004-01-29 | Chemetall Gmbh | Verfahren zur Beschichtung von metallischen Oberflächen und Verwendung der derart beschichteten Substrate |
AU2003250917A1 (en) * | 2002-07-10 | 2004-02-02 | Chemetall Gmbh | Method for coating metallic surfaces |
US20040118483A1 (en) * | 2002-12-24 | 2004-06-24 | Michael Deemer | Process and solution for providing a thin corrosion inhibiting coating on a metallic surface |
DE10322446A1 (de) * | 2003-05-19 | 2004-12-09 | Henkel Kgaa | Vorbehandlung von Metalloberflächen vor einer Lackierung |
DE10323305B4 (de) * | 2003-05-23 | 2006-03-30 | Chemetall Gmbh | Verfahren zur Beschichtung von metallischen Oberflächen mit einer Wasserstoffperoxid enthaltenden Phosphatierungslösung, Phosphatierlösung und Verwendung der behandelten Gegenstände |
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2006
- 2006-11-08 DE DE102006052919A patent/DE102006052919A1/de not_active Withdrawn
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2007
- 2007-09-13 WO PCT/EP2007/059628 patent/WO2008055726A1/fr active Application Filing
- 2007-09-13 BR BRPI0718578-2A patent/BRPI0718578A2/pt not_active Application Discontinuation
- 2007-09-13 RU RU2009121446/02A patent/RU2464356C2/ru not_active IP Right Cessation
- 2007-09-13 PL PL07820181T patent/PL2092090T3/pl unknown
- 2007-09-13 JP JP2009535644A patent/JP5406723B2/ja not_active Expired - Fee Related
- 2007-09-13 CN CN2007800414397A patent/CN101535528B/zh active Active
- 2007-09-13 CA CA2669042A patent/CA2669042C/fr active Active
- 2007-09-13 KR KR1020097009359A patent/KR20090086405A/ko active Search and Examination
- 2007-09-13 EP EP07820181A patent/EP2092090B1/fr active Active
- 2007-09-13 SI SI200731183T patent/SI2092090T1/sl unknown
- 2007-09-13 ES ES07820181T patent/ES2398594T3/es active Active
-
2009
- 2009-04-22 US US12/427,785 patent/US8801871B2/en active Active
- 2009-05-07 ZA ZA200903169A patent/ZA200903169B/xx unknown
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- 2012-03-19 US US13/423,558 patent/US8956468B2/en active Active
Cited By (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
EP2824213A1 (fr) | 2013-07-12 | 2015-01-14 | Voestalpine Stahl GmbH | Procédé d'amélioration de l'adhérence sur une tôle d'acier dotée d'un revêtement de protection |
US9920430B2 (en) | 2013-07-12 | 2018-03-20 | Voestalpine Stahl Gmbh | Method for improving adherence |
Also Published As
Publication number | Publication date |
---|---|
JP5406723B2 (ja) | 2014-02-05 |
CN101535528B (zh) | 2012-03-21 |
US8956468B2 (en) | 2015-02-17 |
RU2464356C2 (ru) | 2012-10-20 |
ZA200903169B (en) | 2010-04-28 |
EP2092090A1 (fr) | 2009-08-26 |
US8801871B2 (en) | 2014-08-12 |
WO2008055726A1 (fr) | 2008-05-15 |
DE102006052919A1 (de) | 2008-05-15 |
US20120177946A1 (en) | 2012-07-12 |
JP2010509499A (ja) | 2010-03-25 |
BRPI0718578A2 (pt) | 2014-03-11 |
KR20090086405A (ko) | 2009-08-12 |
ES2398594T3 (es) | 2013-03-20 |
CA2669042C (fr) | 2016-08-02 |
CA2669042A1 (fr) | 2008-05-15 |
US20090255608A1 (en) | 2009-10-15 |
RU2009121446A (ru) | 2010-12-20 |
CN101535528A (zh) | 2009-09-16 |
SI2092090T1 (sl) | 2013-06-28 |
PL2092090T3 (pl) | 2013-05-31 |
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