WO2005021822A1 - Verfahren zum herstellen eines gehärteten stahlbauteils - Google Patents
Verfahren zum herstellen eines gehärteten stahlbauteils Download PDFInfo
- Publication number
- WO2005021822A1 WO2005021822A1 PCT/EP2004/006251 EP2004006251W WO2005021822A1 WO 2005021822 A1 WO2005021822 A1 WO 2005021822A1 EP 2004006251 W EP2004006251 W EP 2004006251W WO 2005021822 A1 WO2005021822 A1 WO 2005021822A1
- Authority
- WO
- WIPO (PCT)
- Prior art keywords
- zinc
- coating
- corrosion protection
- sheet
- protection layer
- Prior art date
Links
- 238000004519 manufacturing process Methods 0.000 title claims abstract description 10
- 229910000760 Hardened steel Inorganic materials 0.000 title claims abstract description 8
- 239000011701 zinc Substances 0.000 claims abstract description 136
- 238000000576 coating method Methods 0.000 claims abstract description 124
- 229910052725 zinc Inorganic materials 0.000 claims abstract description 113
- HCHKCACWOHOZIP-UHFFFAOYSA-N Zinc Chemical compound [Zn] HCHKCACWOHOZIP-UHFFFAOYSA-N 0.000 claims abstract description 111
- 229910000831 Steel Inorganic materials 0.000 claims abstract description 105
- 238000005260 corrosion Methods 0.000 claims abstract description 105
- 239000010959 steel Substances 0.000 claims abstract description 105
- 230000007797 corrosion Effects 0.000 claims abstract description 104
- 239000011248 coating agent Substances 0.000 claims abstract description 102
- 238000010438 heat treatment Methods 0.000 claims abstract description 31
- QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical compound [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 claims abstract description 26
- 229910052760 oxygen Inorganic materials 0.000 claims abstract description 26
- 239000001301 oxygen Substances 0.000 claims abstract description 26
- 238000001816 cooling Methods 0.000 claims abstract description 14
- 230000008859 change Effects 0.000 claims abstract description 3
- 229910000851 Alloy steel Inorganic materials 0.000 claims abstract 2
- XEEYBQQBJWHFJM-UHFFFAOYSA-N Iron Chemical compound [Fe] XEEYBQQBJWHFJM-UHFFFAOYSA-N 0.000 claims description 93
- 238000000034 method Methods 0.000 claims description 58
- 229910052782 aluminium Inorganic materials 0.000 claims description 44
- XAGFODPZIPBFFR-UHFFFAOYSA-N aluminium Chemical compound [Al] XAGFODPZIPBFFR-UHFFFAOYSA-N 0.000 claims description 44
- 229910052742 iron Inorganic materials 0.000 claims description 30
- 229910052751 metal Inorganic materials 0.000 claims description 30
- 239000002184 metal Substances 0.000 claims description 30
- 239000000203 mixture Substances 0.000 claims description 19
- 230000008569 process Effects 0.000 claims description 17
- 238000004210 cathodic protection Methods 0.000 claims description 13
- PXHVJJICTQNCMI-UHFFFAOYSA-N Nickel Chemical compound [Ni] PXHVJJICTQNCMI-UHFFFAOYSA-N 0.000 claims description 12
- 229910052710 silicon Inorganic materials 0.000 claims description 11
- 239000010703 silicon Substances 0.000 claims description 10
- 229910052748 manganese Inorganic materials 0.000 claims description 8
- 239000011572 manganese Substances 0.000 claims description 8
- 239000010936 titanium Substances 0.000 claims description 8
- 229910052719 titanium Inorganic materials 0.000 claims description 8
- ZOXJGFHDIHLPTG-UHFFFAOYSA-N Boron Chemical compound [B] ZOXJGFHDIHLPTG-UHFFFAOYSA-N 0.000 claims description 7
- PWHULOQIROXLJO-UHFFFAOYSA-N Manganese Chemical compound [Mn] PWHULOQIROXLJO-UHFFFAOYSA-N 0.000 claims description 7
- RTAQQCXQSZGOHL-UHFFFAOYSA-N Titanium Chemical compound [Ti] RTAQQCXQSZGOHL-UHFFFAOYSA-N 0.000 claims description 7
- 229910052796 boron Inorganic materials 0.000 claims description 7
- 239000011777 magnesium Substances 0.000 claims description 6
- 229910052749 magnesium Inorganic materials 0.000 claims description 6
- 229910001092 metal group alloy Inorganic materials 0.000 claims description 6
- 229910052759 nickel Inorganic materials 0.000 claims description 6
- OYPRJOBELJOOCE-UHFFFAOYSA-N Calcium Chemical compound [Ca] OYPRJOBELJOOCE-UHFFFAOYSA-N 0.000 claims description 5
- FYYHWMGAXLPEAU-UHFFFAOYSA-N Magnesium Chemical compound [Mg] FYYHWMGAXLPEAU-UHFFFAOYSA-N 0.000 claims description 5
- 229910052791 calcium Inorganic materials 0.000 claims description 5
- 239000011575 calcium Substances 0.000 claims description 5
- 238000000151 deposition Methods 0.000 claims description 4
- 239000012535 impurity Substances 0.000 claims description 4
- 229910001338 liquidmetal Inorganic materials 0.000 claims description 4
- 230000008021 deposition Effects 0.000 claims description 3
- 238000007740 vapor deposition Methods 0.000 claims description 3
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 claims description 2
- VYZAMTAEIAYCRO-UHFFFAOYSA-N Chromium Chemical compound [Cr] VYZAMTAEIAYCRO-UHFFFAOYSA-N 0.000 claims description 2
- ZOKXTWBITQBERF-UHFFFAOYSA-N Molybdenum Chemical compound [Mo] ZOKXTWBITQBERF-UHFFFAOYSA-N 0.000 claims description 2
- OAICVXFJPJFONN-UHFFFAOYSA-N Phosphorus Chemical compound [P] OAICVXFJPJFONN-UHFFFAOYSA-N 0.000 claims description 2
- NINIDFKCEFEMDL-UHFFFAOYSA-N Sulfur Chemical compound [S] NINIDFKCEFEMDL-UHFFFAOYSA-N 0.000 claims description 2
- 238000005275 alloying Methods 0.000 claims description 2
- 229910052799 carbon Inorganic materials 0.000 claims description 2
- 229910052804 chromium Inorganic materials 0.000 claims description 2
- 239000011651 chromium Substances 0.000 claims description 2
- 239000010960 cold rolled steel Substances 0.000 claims description 2
- 230000001939 inductive effect Effects 0.000 claims description 2
- 229910052750 molybdenum Inorganic materials 0.000 claims description 2
- 239000011733 molybdenum Substances 0.000 claims description 2
- 229910052698 phosphorus Inorganic materials 0.000 claims description 2
- 239000011574 phosphorus Substances 0.000 claims description 2
- 229910052717 sulfur Inorganic materials 0.000 claims description 2
- 239000011593 sulfur Substances 0.000 claims description 2
- WFKWXMTUELFFGS-UHFFFAOYSA-N tungsten Chemical compound [W] WFKWXMTUELFFGS-UHFFFAOYSA-N 0.000 claims description 2
- 229910052721 tungsten Inorganic materials 0.000 claims description 2
- 239000010937 tungsten Substances 0.000 claims description 2
- 229910052720 vanadium Inorganic materials 0.000 claims description 2
- LEONUFNNVUYDNQ-UHFFFAOYSA-N vanadium atom Chemical compound [V] LEONUFNNVUYDNQ-UHFFFAOYSA-N 0.000 claims description 2
- PMVSDNDAUGGCCE-TYYBGVCCSA-L Ferrous fumarate Chemical compound [Fe+2].[O-]C(=O)\C=C\C([O-])=O PMVSDNDAUGGCCE-TYYBGVCCSA-L 0.000 claims 1
- 229910045601 alloy Inorganic materials 0.000 abstract description 9
- 239000000956 alloy Substances 0.000 abstract description 9
- 239000010410 layer Substances 0.000 description 94
- 239000000463 material Substances 0.000 description 23
- 238000000137 annealing Methods 0.000 description 22
- 230000004888 barrier function Effects 0.000 description 20
- 238000004090 dissolution Methods 0.000 description 20
- 238000005259 measurement Methods 0.000 description 19
- 238000009792 diffusion process Methods 0.000 description 13
- 230000001681 protective effect Effects 0.000 description 13
- 239000011241 protective layer Substances 0.000 description 12
- 230000003647 oxidation Effects 0.000 description 11
- 238000007254 oxidation reaction Methods 0.000 description 11
- 230000015572 biosynthetic process Effects 0.000 description 10
- 238000001000 micrograph Methods 0.000 description 10
- -1 aluminum-zinc-silicon Chemical compound 0.000 description 8
- 238000010586 diagram Methods 0.000 description 8
- XUIMIQQOPSSXEZ-UHFFFAOYSA-N Silicon Chemical compound [Si] XUIMIQQOPSSXEZ-UHFFFAOYSA-N 0.000 description 7
- 230000001965 increasing effect Effects 0.000 description 7
- XLOMVQKBTHCTTD-UHFFFAOYSA-N Zinc monoxide Chemical compound [Zn]=O XLOMVQKBTHCTTD-UHFFFAOYSA-N 0.000 description 6
- 238000005246 galvanizing Methods 0.000 description 6
- 238000001336 glow discharge atomic emission spectroscopy Methods 0.000 description 6
- 150000002739 metals Chemical class 0.000 description 6
- 239000002344 surface layer Substances 0.000 description 6
- 229910000640 Fe alloy Inorganic materials 0.000 description 5
- 229910001297 Zn alloy Inorganic materials 0.000 description 5
- PNEYBMLMFCGWSK-UHFFFAOYSA-N aluminium oxide Inorganic materials [O-2].[O-2].[O-2].[Al+3].[Al+3] PNEYBMLMFCGWSK-UHFFFAOYSA-N 0.000 description 5
- 230000007547 defect Effects 0.000 description 5
- 230000000694 effects Effects 0.000 description 5
- 239000003792 electrolyte Substances 0.000 description 5
- 238000011156 evaluation Methods 0.000 description 5
- 230000006870 function Effects 0.000 description 5
- KFZAUHNPPZCSCR-UHFFFAOYSA-N iron zinc Chemical compound [Fe].[Zn] KFZAUHNPPZCSCR-UHFFFAOYSA-N 0.000 description 5
- 229910018072 Al 2 O 3 Inorganic materials 0.000 description 4
- 229910000680 Aluminized steel Inorganic materials 0.000 description 4
- FJMNNXLGOUYVHO-UHFFFAOYSA-N aluminum zinc Chemical compound [Al].[Zn] FJMNNXLGOUYVHO-UHFFFAOYSA-N 0.000 description 4
- 238000005868 electrolysis reaction Methods 0.000 description 4
- 239000007788 liquid Substances 0.000 description 4
- 239000000155 melt Substances 0.000 description 4
- TWNQGVIAIRXVLR-UHFFFAOYSA-N oxo(oxoalumanyloxy)alumane Chemical compound O=[Al]O[Al]=O TWNQGVIAIRXVLR-UHFFFAOYSA-N 0.000 description 4
- 238000012545 processing Methods 0.000 description 4
- 241000282373 Panthera pardus Species 0.000 description 3
- 238000006243 chemical reaction Methods 0.000 description 3
- 238000010276 construction Methods 0.000 description 3
- 238000003618 dip coating Methods 0.000 description 3
- 238000007598 dipping method Methods 0.000 description 3
- 230000001976 improved effect Effects 0.000 description 3
- 239000007769 metal material Substances 0.000 description 3
- 238000000550 scanning electron microscopy energy dispersive X-ray spectroscopy Methods 0.000 description 3
- 239000000126 substance Substances 0.000 description 3
- 239000000758 substrate Substances 0.000 description 3
- 239000011787 zinc oxide Substances 0.000 description 3
- 229910000838 Al alloy Inorganic materials 0.000 description 2
- IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 description 2
- 229910000676 Si alloy Inorganic materials 0.000 description 2
- FAPWRFPIFSIZLT-UHFFFAOYSA-M Sodium chloride Chemical compound [Na+].[Cl-] FAPWRFPIFSIZLT-UHFFFAOYSA-M 0.000 description 2
- 229910007570 Zn-Al Inorganic materials 0.000 description 2
- 230000002051 biphasic effect Effects 0.000 description 2
- 238000001354 calcination Methods 0.000 description 2
- 238000005261 decarburization Methods 0.000 description 2
- 238000001514 detection method Methods 0.000 description 2
- 238000011161 development Methods 0.000 description 2
- 230000018109 developmental process Effects 0.000 description 2
- 238000009826 distribution Methods 0.000 description 2
- 230000008020 evaporation Effects 0.000 description 2
- 238000001704 evaporation Methods 0.000 description 2
- 239000007789 gas Substances 0.000 description 2
- 238000002844 melting Methods 0.000 description 2
- 230000008018 melting Effects 0.000 description 2
- BASFCYQUMIYNBI-UHFFFAOYSA-N platinum Chemical compound [Pt] BASFCYQUMIYNBI-UHFFFAOYSA-N 0.000 description 2
- 230000005855 radiation Effects 0.000 description 2
- 239000007787 solid Substances 0.000 description 2
- 238000012360 testing method Methods 0.000 description 2
- 230000009466 transformation Effects 0.000 description 2
- 230000007704 transition Effects 0.000 description 2
- RYGMFSIKBFXOCR-UHFFFAOYSA-N Copper Chemical compound [Cu] RYGMFSIKBFXOCR-UHFFFAOYSA-N 0.000 description 1
- 229910001335 Galvanized steel Inorganic materials 0.000 description 1
- 229910004298 SiO 2 Inorganic materials 0.000 description 1
- 229910021607 Silver chloride Inorganic materials 0.000 description 1
- ATJFFYVFTNAWJD-UHFFFAOYSA-N Tin Chemical compound [Sn] ATJFFYVFTNAWJD-UHFFFAOYSA-N 0.000 description 1
- 229910000611 Zinc aluminium Inorganic materials 0.000 description 1
- 238000009825 accumulation Methods 0.000 description 1
- HXFVOUUOTHJFPX-UHFFFAOYSA-N alumane;zinc Chemical compound [AlH3].[Zn] HXFVOUUOTHJFPX-UHFFFAOYSA-N 0.000 description 1
- CSDREXVUYHZDNP-UHFFFAOYSA-N alumanylidynesilicon Chemical compound [Al].[Si] CSDREXVUYHZDNP-UHFFFAOYSA-N 0.000 description 1
- 238000005269 aluminizing Methods 0.000 description 1
- CYUOWZRAOZFACA-UHFFFAOYSA-N aluminum iron Chemical compound [Al].[Fe] CYUOWZRAOZFACA-UHFFFAOYSA-N 0.000 description 1
- 238000004458 analytical method Methods 0.000 description 1
- 238000013459 approach Methods 0.000 description 1
- 239000007864 aqueous solution Substances 0.000 description 1
- 230000000903 blocking effect Effects 0.000 description 1
- 239000011247 coating layer Substances 0.000 description 1
- 238000005097 cold rolling Methods 0.000 description 1
- 229910052802 copper Inorganic materials 0.000 description 1
- 239000010949 copper Substances 0.000 description 1
- 230000002950 deficient Effects 0.000 description 1
- 239000008367 deionised water Substances 0.000 description 1
- 229910021641 deionized water Inorganic materials 0.000 description 1
- 230000001419 dependent effect Effects 0.000 description 1
- 230000006866 deterioration Effects 0.000 description 1
- 230000001627 detrimental effect Effects 0.000 description 1
- 238000007922 dissolution test Methods 0.000 description 1
- 238000002848 electrochemical method Methods 0.000 description 1
- 238000004070 electrodeposition Methods 0.000 description 1
- 238000009713 electroplating Methods 0.000 description 1
- 238000002474 experimental method Methods 0.000 description 1
- 230000002349 favourable effect Effects 0.000 description 1
- 239000007888 film coating Substances 0.000 description 1
- 238000009501 film coating Methods 0.000 description 1
- 239000008397 galvanized steel Substances 0.000 description 1
- 238000005244 galvannealing Methods 0.000 description 1
- 230000035876 healing Effects 0.000 description 1
- 238000007731 hot pressing Methods 0.000 description 1
- 238000005098 hot rolling Methods 0.000 description 1
- 239000003112 inhibitor Substances 0.000 description 1
- 230000005764 inhibitory process Effects 0.000 description 1
- 238000011835 investigation Methods 0.000 description 1
- UQSXHKLRYXJYBZ-UHFFFAOYSA-N iron oxide Inorganic materials [Fe]=O UQSXHKLRYXJYBZ-UHFFFAOYSA-N 0.000 description 1
- 235000013980 iron oxide Nutrition 0.000 description 1
- VBMVTYDPPZVILR-UHFFFAOYSA-N iron(2+);oxygen(2-) Chemical class [O-2].[Fe+2] VBMVTYDPPZVILR-UHFFFAOYSA-N 0.000 description 1
- 230000001050 lubricating effect Effects 0.000 description 1
- 239000011159 matrix material Substances 0.000 description 1
- 230000007246 mechanism Effects 0.000 description 1
- 238000013508 migration Methods 0.000 description 1
- 230000005012 migration Effects 0.000 description 1
- QELJHCBNGDEXLD-UHFFFAOYSA-N nickel zinc Chemical compound [Ni].[Zn] QELJHCBNGDEXLD-UHFFFAOYSA-N 0.000 description 1
- 229910052757 nitrogen Inorganic materials 0.000 description 1
- 229910000510 noble metal Inorganic materials 0.000 description 1
- 230000003287 optical effect Effects 0.000 description 1
- 230000001590 oxidative effect Effects 0.000 description 1
- 239000003973 paint Substances 0.000 description 1
- 238000005554 pickling Methods 0.000 description 1
- 229910052697 platinum Inorganic materials 0.000 description 1
- 239000011148 porous material Substances 0.000 description 1
- 239000010970 precious metal Substances 0.000 description 1
- 239000011253 protective coating Substances 0.000 description 1
- 230000009993 protective function Effects 0.000 description 1
- 238000004080 punching Methods 0.000 description 1
- 239000000376 reactant Substances 0.000 description 1
- 230000000630 rising effect Effects 0.000 description 1
- 238000005488 sandblasting Methods 0.000 description 1
- 238000007790 scraping Methods 0.000 description 1
- 238000007493 shaping process Methods 0.000 description 1
- 229910052709 silver Inorganic materials 0.000 description 1
- HKZLPVFGJNLROG-UHFFFAOYSA-M silver monochloride Chemical compound [Cl-].[Ag+] HKZLPVFGJNLROG-UHFFFAOYSA-M 0.000 description 1
- 238000004513 sizing Methods 0.000 description 1
- 239000011780 sodium chloride Substances 0.000 description 1
- 238000003856 thermoforming Methods 0.000 description 1
- 239000011135 tin Substances 0.000 description 1
- 229910052718 tin Inorganic materials 0.000 description 1
- 238000012546 transfer Methods 0.000 description 1
- 239000002966 varnish Substances 0.000 description 1
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Chemical compound O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 1
- 150000003751 zinc Chemical class 0.000 description 1
- WGEATSXPYVGFCC-UHFFFAOYSA-N zinc ferrite Chemical compound O=[Zn].O=[Fe]O[Fe]=O WGEATSXPYVGFCC-UHFFFAOYSA-N 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
- C23C2/00—Hot-dipping or immersion processes for applying the coating material in the molten state without affecting the shape; Apparatus therefor
- C23C2/02—Pretreatment of the material to be coated, e.g. for coating on selected surface areas
- C23C2/022—Pretreatment of the material to be coated, e.g. for coating on selected surface areas by heating
- C23C2/0224—Two or more thermal pretreatments
-
- C—CHEMISTRY; METALLURGY
- C21—METALLURGY OF IRON
- C21D—MODIFYING THE PHYSICAL STRUCTURE OF FERROUS METALS; GENERAL DEVICES FOR HEAT TREATMENT OF FERROUS OR NON-FERROUS METALS OR ALLOYS; MAKING METAL MALLEABLE, e.g. BY DECARBURISATION OR TEMPERING
- C21D1/00—General methods or devices for heat treatment, e.g. annealing, hardening, quenching or tempering
- C21D1/62—Quenching devices
- C21D1/673—Quenching devices for die quenching
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B21—MECHANICAL METAL-WORKING WITHOUT ESSENTIALLY REMOVING MATERIAL; PUNCHING METAL
- B21D—WORKING OR PROCESSING OF SHEET METAL OR METAL TUBES, RODS OR PROFILES WITHOUT ESSENTIALLY REMOVING MATERIAL; PUNCHING METAL
- B21D22/00—Shaping without cutting, by stamping, spinning, or deep-drawing
- B21D22/02—Stamping using rigid devices or tools
- B21D22/04—Stamping using rigid devices or tools for dimpling
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B21—MECHANICAL METAL-WORKING WITHOUT ESSENTIALLY REMOVING MATERIAL; PUNCHING METAL
- B21J—FORGING; HAMMERING; PRESSING METAL; RIVETING; FORGE FURNACES
- B21J5/00—Methods for forging, hammering, or pressing; Special equipment or accessories therefor
-
- 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
- C23C2/00—Hot-dipping or immersion processes for applying the coating material in the molten state without affecting the shape; Apparatus therefor
- C23C2/04—Hot-dipping or immersion processes for applying the coating material in the molten state without affecting the shape; Apparatus therefor characterised by the coating material
- C23C2/06—Zinc or cadmium or alloys based thereon
-
- 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
- C23C2/00—Hot-dipping or immersion processes for applying the coating material in the molten state without affecting the shape; Apparatus therefor
- C23C2/26—After-treatment
- C23C2/28—Thermal after-treatment, e.g. treatment in oil bath
- C23C2/29—Cooling or quenching
-
- 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
- C23C2/00—Hot-dipping or immersion processes for applying the coating material in the molten state without affecting the shape; Apparatus therefor
- C23C2/34—Hot-dipping or immersion processes for applying the coating material in the molten state without affecting the shape; Apparatus therefor characterised by the shape of the material to be treated
- C23C2/36—Elongated material
- C23C2/40—Plates; Strips
-
- C—CHEMISTRY; METALLURGY
- C25—ELECTROLYTIC OR ELECTROPHORETIC PROCESSES; APPARATUS THEREFOR
- C25D—PROCESSES FOR THE ELECTROLYTIC OR ELECTROPHORETIC PRODUCTION OF COATINGS; ELECTROFORMING; APPARATUS THEREFOR
- C25D5/00—Electroplating characterised by the process; Pretreatment or after-treatment of workpieces
- C25D5/34—Pretreatment of metallic surfaces to be electroplated
- C25D5/36—Pretreatment of metallic surfaces to be electroplated of iron or steel
-
- C—CHEMISTRY; METALLURGY
- C25—ELECTROLYTIC OR ELECTROPHORETIC PROCESSES; APPARATUS THEREFOR
- C25D—PROCESSES FOR THE ELECTROLYTIC OR ELECTROPHORETIC PRODUCTION OF COATINGS; ELECTROFORMING; APPARATUS THEREFOR
- C25D5/00—Electroplating characterised by the process; Pretreatment or after-treatment of workpieces
- C25D5/48—After-treatment of electroplated surfaces
-
- C—CHEMISTRY; METALLURGY
- C21—METALLURGY OF IRON
- C21D—MODIFYING THE PHYSICAL STRUCTURE OF FERROUS METALS; GENERAL DEVICES FOR HEAT TREATMENT OF FERROUS OR NON-FERROUS METALS OR ALLOYS; MAKING METAL MALLEABLE, e.g. BY DECARBURISATION OR TEMPERING
- C21D2221/00—Treating localised areas of an article
-
- C—CHEMISTRY; METALLURGY
- C21—METALLURGY OF IRON
- C21D—MODIFYING THE PHYSICAL STRUCTURE OF FERROUS METALS; GENERAL DEVICES FOR HEAT TREATMENT OF FERROUS OR NON-FERROUS METALS OR ALLOYS; MAKING METAL MALLEABLE, e.g. BY DECARBURISATION OR TEMPERING
- C21D2251/00—Treating composite or clad material
- C21D2251/02—Clad material
-
- C—CHEMISTRY; METALLURGY
- C21—METALLURGY OF IRON
- C21D—MODIFYING THE PHYSICAL STRUCTURE OF FERROUS METALS; GENERAL DEVICES FOR HEAT TREATMENT OF FERROUS OR NON-FERROUS METALS OR ALLOYS; MAKING METAL MALLEABLE, e.g. BY DECARBURISATION OR TEMPERING
- C21D9/00—Heat treatment, e.g. annealing, hardening, quenching or tempering, adapted for particular articles; Furnaces therefor
- C21D9/46—Heat treatment, e.g. annealing, hardening, quenching or tempering, adapted for particular articles; Furnaces therefor for sheet metals
-
- 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
- Y10T29/00—Metal working
- Y10T29/49—Method of mechanical manufacture
- Y10T29/4998—Combined manufacture including applying or shaping of fluent material
- Y10T29/49982—Coating
-
- 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
- Y10T29/00—Metal working
- Y10T29/49—Method of mechanical manufacture
- Y10T29/49995—Shaping one-piece blank by removing material
-
- 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.]
- Y10T428/12771—Transition metal-base component
- Y10T428/12785—Group IIB metal-base component
- Y10T428/12792—Zn-base component
- Y10T428/12799—Next to Fe-base component [e.g., galvanized]
-
- 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
- Y10T428/31504—Composite [nonstructural laminate]
- Y10T428/31678—Of metal
Definitions
- the invention relates to a method for producing a hardened steel component with cathodic corrosion protection, as well as a corrosion protection for steel sheets, as well as components made of steel sheets with the corrosion protection.
- Low alloyed steel sheets are not resistant to corrosion after being produced by suitable forming steps, either by hot rolling or cold rolling. This means that oxidation sets in after a relatively short time and due to the humidity on the surface.
- a corrosion protection layer is a layer produced on a metal or in the near-surface region of a metal, which consists of one or more layers. Multi-layer coatings are also referred to as corrosion protection systems.
- Possible corrosion protection layers are, for example, organic coatings, inorganic coatings and metallic coatings.
- the purpose of metallic corrosion protection layers is to transfer the properties of the support material to the steel surface for as long as possible. Accordingly, the choice of an effective metallic corrosion protection requires the knowledge of the corrosion-chemical relationships in the system steel / coating metal / attacking medium.
- the coating metals can be electrochemically nobler or electrochemically less noble than steel.
- the respective coating metal protects the steel only through the formation of protective layers.
- barrier protection As soon as the surface of the coating metal has pores or was injured, a "local element" forms in the presence of moisture, in which the base partner is attacked by the metal to be protected.
- the more noble coating metals include tin, nickel and copper.
- Metallic protective layers are applied by various methods. Depending on the metal and process, the connection of the steel surface is chemical, physical or mechanical and ranges from alloy formation and diffusion to adhesion and mere mechanical clamping.
- the metallic coatings are said to have similar technological and mechanical properties to steel as they do to steel, and to behave similarly to steel in terms of mechanical stress or plastic deformation. Accordingly, the coatings should not be damaged during forming and should not be affected by forming operations.
- the metal to be protected is immersed in molten metal melts. Due to the hot dipping, corresponding alloy layers are formed at the phase boundary of steel coating metal.
- An example of this is the hot dip galvanizing.
- Hot-dip galvanized products have high corrosion resistance, good weldability and formability, and their main applications are the construction, automotive and household appliance industries.
- the production of a coating of a zinc-iron alloy is known. For this purpose, these products are subjected to a diffusion annealing at temperatures above the zinc melting point, usually between 480 ° C and 550 ° C after hot-dip galvanizing.
- the zinc-iron alloy layers grow and absorb the overlying zinc layer. This process is called "galvannealing".
- the zinc-iron alloy thus produced also has a high corrosion resistance, good weldability and formability.
- Main applications are the automotive and home appliance industry.
- other coatings of aluminum, aluminum-silicon, zinc-aluminum and aluminum-zinc-silicon can be produced by hot dipping.
- electrodeposited metal coatings i. the electrolytic, so under current passage deposition of metallic coatings of electrolytes.
- electrolytic coating is also possible with such metals, which can not be applied by hot dip process.
- Conventional layer thicknesses in electrolytic coatings are usually between 2.5 and 10 microns, they are thus generally lower than hot-dip coatings.
- Some metals, e.g. Zinc, also allow thick film coatings with electrolytic coating.
- Electrolytically galvanized sheets are mainly used in the automotive industry, because of the high surface quality, these sheets are used above all in the outer skin area. They have good formability, weldability and storability as well as good paintable and matt surfaces.
- the sheet is scaled by heating superficial, so that after forming and hardening the sheet surface are cleaned uss, for example by sandblasting. Then the sheet is trimmed and, if necessary, necessary holes are punched. In this case, it is disadvantageous that the sheets have a very high hardness in the mechanical processing and therefore the processing is complicated and in particular a high tool wear exists.
- US 6,564,604 B2 The purpose of US 6,564,604 B2 is to provide steel sheets which are subsequently subjected to a heat treatment, and to provide a method of producing parts by press-hardening these coated steel sheets. In this case, in spite of the temperature increase, it should be ensured that the steel sheet is not decarburized and the surface of the steel sheet is not oxidized before, during and after the hot pressing or the heat treatment.
- an alloyed intermetallic mixture should be applied to the surface before or after punching, which should provide protection against corrosion and decarburization and also can provide a lubricating function.
- this document proposes to use a customary, apparently electrolytically applied zinc layer, wherein this zinc layer is to be converted into a homogeneous Zn-Fe alloy layer with the steel substrate in a subsequent austenizing of the sheet substrate.
- This homogeneous layer structure is confirmed by microscopic images. Contrary to previous assumptions, this coating is said to have a mechanical resistance that prevents it from melting. In practice, however, such an effect does not show.
- the use of zinc or zinc alloys is said to provide cathodic protection of the edges when Cuts are available.
- US Pat. No. 6,564,604 B2 specifies a coating consisting of 50% to 55% aluminum and 45% to 50% zinc, with possibly small amounts of silicon. Such a coating is not new in itself and known under the brand name Galvalume®. It is stated that the coating metals zinc and aluminum with iron should form a homogeneous zinc-aluminum-iron alloy coating. In the case of this coating, it is disadvantageous that adequate cathodic corrosion protection is no longer achieved here, but the predominant barrier protection which is thereby achieved is not sufficient for use in the press hardening process, since partial surface damage to the surface is unavoidable.
- the method described in this document is unable to solve the problem that, in general, zinc-based cathodic corrosion coatings are not suitable for protecting steel sheets which are to be subjected to a heat treatment after coating and may also be subjected to a further shaping or forming step.
- EP 1 013 785 A1 discloses a method for producing a sheet-metal component, wherein the sheet is to have an aluminum layer or an aluminum alloy layer on the surface.
- a sheet provided with such coatings is to be subjected to a press hardening process, wherein possible coating alloys are mentioned Alloy with 9-10% silicon, 2-3.5% iron, balance aluminum with impurities and a second alloy with 2-4% iron and the balance aluminum with impurities.
- Such coatings are known per se and correspond to the coating of a hot-dip aluminized steel sheet. In such a coating is disadvantageous in that only a so-called barrier protection is achieved. The moment that such a barrier layer is damaged or cracked in the Fe-Al layer, the base material, in this case the steel, is attacked and corroded. A cathodic protective effect is absent.
- DE 102 46 614 A1 therefore proposes applying a coating as metal or a metal alloy by means of a galvanic coating process in organic, non-aqueous solution, where a coating material which is particularly suitable and therefore preferred is aluminum or an aluminum alloy. Alternatively, zinc or zinc alloys would be suitable. Such a coated sheet can then be cold preformed and hot finished molded.
- this method has the disadvantage that an aluminum coating, even if it has been applied by electrolysis, no longer offers any protection against corrosion if the surface of the finished component is damaged, since the protective barrier has been breached.
- an electrodeposited zinc coating it is disadvantageous that during heating for hot forming, the zinc is largely oxidized and no longer available for cathodic protection. Under a protective gas atmosphere, the zinc evaporates.
- the object of the invention is to provide a method for producing a component from hardened steel sheet with an improved cathodic corrosion protection.
- Another object is to provide a cathodic corrosion protection for steel sheets, which are subjected to forming and hardening.
- the object is achieved with a corrosion protection with the features of claim 27.
- the inventive method provides, on a hardenable steel sheet a coating of a mixture consisting essentially of zinc and one or more oxygen-affine elements such as magnesium, silicon, titanium, calcium, aluminum, boron and manganese with a content of 0.1 to 15 wt .-% of the Sauerstoffäffinen element and to heat the coated steel sheet at least partially under the admission of oxygen to a temperature above the austenitization temperature of the sheet metal alloy and before or subsequently reshape, the sheet is cooled after sufficient heating and the Cooling rate is measured so that hardening of the sheet metal alloy takes place.
- a hardened component is obtained from a steel sheet having a good cathodic corrosion protection.
- the corrosion protection according to the invention for steel sheets, which are first subjected to a heat treatment and then reformed and thereby hardened, is a cathodic corrosion protection which is essentially based on zinc.
- 0.1% to 15% of one or more oxygen-containing elements such as magnesium, silicon, titanium, calcium, aluminum, boron and manganese or any mixture or alloy thereof are added to the zinc forming the coating. It has been found that such small amounts of an oxygen affinity element as magnesium, silicon, titanium, calcium, aluminum, boron and manganese cause a surprising effect in this particular application.
- at least Mg, Al, Ti, Si, Ca, B, Mn are suitable as oxygen-affine elements. When aluminum is mentioned below, this is representative of the other elements mentioned.
- the application of the coating according to the invention on a steel sheet can be done, for example, by so-called hot-dip galvanizing, i. a hot dip coating is performed wherein a liquid mixture of zinc and the oxygen-affine element (s) is applied. Furthermore, it is possible to electrolytically apply the coating, i. to deposit the mixture of zinc and the oxygen-affine element (s) collectively on the sheet surface or first to deposit a zinc layer and then to deposit on the zinc surface one or more oxygen-affine elements in succession or any mixture or alloy thereof, or by vapor deposition or other suitable method deposit.
- an oxygen-containing element in particular aluminum
- an essentially AL 2 0 3 or an oxide of the oxygen-containing element MgO, CaO, TiO, SiO 2 , B 2 0 3 , MnO
- This very thin oxide layer protects the underlying Zn-containing corrosion protection layer from oxidation even at very high temperatures.
- an approximately two-layer corrosion protection layer is formed, which consists of a cathodically highly effective layer, high proportion of zinc and a very thin oxidation protection layer of one or more oxides (AL 2 0 3 , MgO , CaO, TiO, Si0 2 , B 2 0 3 , MnO) to oxidation and Evaporation is protected.
- a 2 0 3 , MgO , CaO, TiO, Si0 2 , B 2 0 3 , MnO oxides
- the corrosion protection layer according to the invention for the press-hardening process also has such a high stability that a forming step following the austenitizing of the sheets does not destroy this layer. Even if microcracks occur on the cured component, however, the cathodic protection effect is at least significantly greater than the protective effect of the known corrosion protection layers for the press-hardening process.
- a zinc alloy with a content of aluminum in weight percent of greater than 0.1 but less than 15%, in particular less than 10%, more preferably less than 5% on a Steel plate, in particular an alloyed steel sheet are applied, whereupon in a second step, parts of the coated sheet are machined and in particular cut out or punched out and heated on access of atmospheric oxygen to a temperature above the Austenitmaschinestemperatur the sheet metal alloy and then cooled at an increased speed.
- a transformation of the cut out of the sheet metal part (the board) can be carried out before or after the heating of the sheet to the Austenitmaschinestemperatur.
- the sheet when coating the sheet to the sheet surface or in the proximal region of the layer, a thin barrier phase consisting in particular of Fe 2 Al 5 _ x Zn x is formed, which impedes the Fe-Zn diffusion in a liquid metal coating process, which takes place in particular at a temperature up to 690 ° C.
- the sheet is formed with a zinc-metal coating with an addition of aluminum, which is effective only towards the sheet surface, as in the proximal region of the support an extremely thin barrier phase, which is effective against rapid growth of an iron-zinc compound phase, having.
- the metal layer on the sheet is liquefied for the time being.
- the oxygenated aluminum from the zinc reacts with atmospheric oxygen to form solid oxide or alumina, resulting in a decrease in the aluminum metal concentration in this direction, which causes a steady diffusion of aluminum towards depletion, ie towards the distal region ,
- This accumulation of toner at the layer area exposed to air now acts as oxidation protection for the layered metal and as an evaporation inhibitor for the zinc.
- the aluminum is withdrawn from the proximal blocking phase by continuous diffusion towards the distal region, where it is available for forming the superficial A1 2 0 3 layer.
- the formation of a sheet metal coating is achieved, which leaves a cathodically highly effective layer with a high zinc content.
- Well suited is, for example, a zinc alloy with a content of aluminum in weight percent of greater than 0.2 but less than 4, preferably greater than 0.26 but less than 2.5 wt .-%.
- the zinc alloy layer is applied to the sheet surface passing through a liquid metal bath at a temperature higher than 425 ° C, but lower than 690 ° C, especially at 440 ° C to 495 ° C, followed by cooling of the coated sheet, not only the proximal barrier phase can be effectively formed, or a very good diffusion inhibition can be observed in the region of the barrier layer, but it also takes place to improve the thermoforming properties of the sheet material.
- An advantageous embodiment of the invention is given in a method in which a hot or cold rolled steel strip having a thickness of, for example, greater than 0.15 mm and a concentration range of at least one of the alloying elements within the limits in wt .-%
- Silicon to 1.9, preferably 0.11 to 1.5
- Chromium to 1.5, preferably 0.1 to 0.9
- Molybdenum to 0.9, preferably 0.1 to 0.5
- Titanium to 0.2, preferably 0.02 to 0.1
- the surface structure of the cathodic corrosion protection according to the invention is particularly favorable for a high adhesion of paints and varnishes.
- FIG. 1 shows a heating curve of test sheets during annealing in a radiation furnace
- Figure 2 micrograph of the cross section of a annealed sample of a non-inventive hot-dip aluminized steel sheet
- FIG. 3 shows the potential curve over the measuring time at a galvanostatic dissolution for a hot-dip aluminized steel sheet not according to the invention
- Figure 4 micrograph of the cross section of a calcined sample of a steel sheet with a non-inventive coating of an aluminum-zinc-silicon alloy
- FIG. 5 shows the potential curve over the measuring time in a galvanostatic dissolution test of a steel sheet not according to the invention with a coating of an aluminum-zinc-silicon alloy
- FIG. 6 micrograph of the transverse section of a heat-treated sample of a cathodic corrosion-protected metal sheet according to the invention
- FIG. 7 shows the potential profile for the sheet according to FIG. 6
- FIG. 8 a micrograph of the cross section of a heat-treated sample of a sheet provided with a cathodic corrosion protection according to the invention
- FIG. 9 shows the potential curve of the sheet according to FIG. 8.
- FIG. 10 micrographs of the surface of a sheet coated in accordance with the invention in the uncured, not thermally treated state according to FIGS. 8 and 9 in comparison with a sheet metal not coated and treated according to the invention;
- FIG. 11 a micrograph of the cross section of a sheet not coated and treated according to the invention.
- FIG. 12 shows the potential profile of the sheet not according to the invention according to FIG. 11;
- FIG. 13 micrograph of the transverse section of a sheet coated and heat-treated according to the invention;
- FIG. 14 shows the potential curve of the sheet according to FIG. 13
- FIG. 15 the micrograph of the cross section of an electrolytically galvanized steel sheet not according to the invention.
- FIG. 16 shows the potential curve of the sheet according to FIG. 15
- FIG. 17 the micrograph of the cross section of a heat-treated sample of a sheet not according to the invention with a zinc-nickel coating
- FIG. 18 shows the potential profile of the sheet not according to FIG. 17;
- Figure 19 a comparison of the potentials required for dissolution as a function of time for the materials tested.
- FIG. 20 a diagram showing the area used for the assessment of the corrosion protection
- FIG. 21 a diagram showing the different protective energies of the tested materials
- FIG. 22 shows a diagram showing the different protective energies of a sheet according to the invention at two different heating conditions;
- FIG. 23 shows qualitatively the phase formation as a "leopard pattern" in coatings according to the invention;
- FIG. 24 a diagram showing possible process sequences according to the invention.
- Figure 25 is a graph showing the distribution of the elements aluminum zinc and iron depending on the depth of the surface layer before the annealing of the sheet;
- Figure 26 is a graph showing the distribution of the elements aluminum zinc and iron depending on the depth of the surface layer after the annealing of the sheet as evidence of the formation of a superficial protective skin of alumina.
- the protection energy is the measure for the electrochemical protection of the layer, determined by galvanostatic dissolution.
- the electrochemical method of galvanostatic dissolution of the metallic surface coatings of a material allows to classify the mechanism of corrosion protection of the layer.
- the potential-time behavior of a corrosion-protective layer is determined for a given constant current flow. For the measurements, a current density of 12.7 mA / cm 2 was specified.
- the measuring arrangement is a three-electrode system.
- the counterelectrode used was a platinum network, the reference electrode consisting of Ag / AgCl (3M).
- the electrolyte consists of 100 g / 1 ZnS0 4 * 5H 2 0 and 200 g / 1 NaCl dissolved in deionized water.
- the barrier protection is characterized by the fact that it separates the base material from the corrosive medium.
- a hot-dip aluminized steel sheet is made by passing a steel sheet through a liquid aluminum bath.
- the reaction of the steel with the aluminum coating produces an aluminum-iron surface layer.
- the corresponding annealed sheet shows a dark gray appearance, the surface is homogeneous and visually shows no defects.
- a very high potential (+ 2.8 V) are applied to ensure the current circuit of 12.7 mA / cm 2. After a short measuring time, the required potential drops to the steel potential. From this behavior, it can be seen that an annealed sheet with a layer obtained by fire aluminizing provides very efficient barrier protection.
- FIG. 3 a micrograph of a cross section in FIG. 2.
- a steel sheet was hot dip galvanized with an aluminum-zinc layer, the melt consisting of 55% aluminum, 44% zinc and about 1% silicon. After the surface coating and subsequent annealing at 900 ° C., a gray-bluish surface appears without defects. A transverse section is shown in FIG.
- the annealed material is then subjected to galvanostatic dissolution.
- the material shows a potential of about -0.92 V, which is necessary for the resolution, and is thus clearly below the steel potential.
- This value is comparable to the potential needed to dissolve a hot dip galvanized coating prior to the annealing process.
- this very zinc-rich phase ends after just about 350 seconds of measurement time. This is followed by a rapid increase to a potential which is now just below the steel is potential.
- the potential After breaking through this layer, the potential first drops to a value of about -0.54 V and then increases continuously to a value of about -0.35 V. Only then does it slowly sink to steel potential.
- This material shows some cathodic corrosion protection due to the very negative potential at the beginning of the measurement, which is well below the steel potential, in addition to the barrier protection.
- the part of the layer that provides cathodic protection against corrosion is used up after only about 350 seconds of measurement time.
- the remaining layer can only offer a low cathodic corrosion protection, since the difference between the required potential for the layer dissolution and the steel potential now only less than 0.12 V. In a poorly conductive electrolyte, this part of the cathodic corrosion protection is no longer usable.
- the potential-time diagram is shown in FIG.
- a steel sheet is hot-dip galvanized with a melt consisting essentially of 95% zinc and 5% aluminum. After annealing, the sheet shows a silvery-gray surface with no defects.
- the cross-section ( Figure 6) shows that the coating consists of a light phase and a dark phase, wherein the. Phases are Zn-Fe-Al-containing phases. The bright phases are more zinc-rich, the dark phases more iron-rich. Part of the aluminum reacted with atmospheric oxygen during the calcination and formed a protective Al 2 O 3 skin.
- the galvanostatic dissolution shows a potential of about -0.7 V required for the resolution. This value is significantly below the potential of the steel. After a measuring time of approx. 1,000 seconds it turns a potential of about -0.6V. This potential is also clearly below the steel potential. After a measurement time of approximately 3,500 seconds, this part of the layer is used up and the necessary potential for dissolving the layer approaches the steel potential. This coating thus offers after the annealing in addition to the barrier protection a cathodic corrosion protection. The potential is up to a measurement time of 3,500 seconds at a value of ⁇ -0.6 V, so that a significant cathodic protection is maintained over a long time, even if the sheet was supplied to the austenitizing temperature.
- the potential-time diagram is shown in FIG.
- the sheet is passed through a melt or through a zinc bath, with a zinc content of 99.8% and an aluminum content of 0.2%.
- Aluminum present in the zinc coating reacts with atmospheric oxygen during the calcination and forms a protective Al 2 O 3 skin. Through constant diffusion of oxygenated aluminum to the surface, this protective skin is maintained and expanded.
- the sheet shows a silvery-gray surface without defects. From the originally about 15 microns thick zinc coating develops during the annealing by diffusion about 20 to 25 microns thick layer, said layer ( Figure 8) consists of a dark appearing phase with a composition Zn / Fe of about 30/70 and out a bright area with the composition Zn / Fe of about 80/20. On the surface of the coating, an increased aluminum content is detectable.
- the annealed material has a potential of approx. -0.75 V. After a measuring time of approx. 1,500 seconds, the potential required for the resolution increases to ⁇ -0.6 V. The phase lasts up to a measuring time of approx. 2,800 seconds. Then the required potential increases to steel potential. In this case too, in addition to barrier protection, there is cathodic corrosion protection. The potential is up to a measurement time of 2,800 seconds at a value of ⁇ -0.6 V. Thus, such a material has thus over a very long time a cathodic corrosion protection.
- the potential-time diagram is shown in FIG.
- the sheet is heated to a temperature of about 500 ° C after exiting the metal strip from the molten zinc (about 450 ° C strip temperature).
- the zinc layer is completely converted into Zn-Fe phases.
- the zinc layer is thus wholly, i. converted to Zn-Fe phases to the surface.
- This anticorrosive layer contains some aluminum in the zinc bath, of the order of about 0.13%.
- a 1 mm thick steel sheet with said heat treated and fully converted coating is heated for 4 minutes and 30 seconds in a 900 ° C oven.
- the result is a yellow-green surface.
- the yellow-green surface indicates oxidation of the Zn-Fe phases during annealing.
- An aluminum oxide protective layer is undetectable. The reason for the absence of an aluminum oxide protective layer can be explained by the fact that in the Annealing treatment due to solid Zn-Fe phases, aluminum can not migrate to the surface so rapidly and protect the Zn-Fe coating from oxidation. When heating this material at temperatures around 500 ° C is still no liquid zinc-rich phase, because this forms only at higher temperatures of 782 ° C. When reaching 782 ° C, thermodynamically there is a liquid zinc-rich phase in which the aluminum is freely available. Nevertheless, the surface layer is not protected against oxidation.
- the corrosion protection layer is already partially oxidized before and it can no longer form opaque alumina skin.
- the layer is wavy ragged in cross-section and consists of Zn and Zn-Fe oxides (Figure 11).
- the surface of said material is much larger due to the highly crystalline, acicular surface finish of the surface, which could also be detrimental to the formation of a covering and thicker alumina protective layer.
- the said non-inventive coating forms in the initial state, ie not in the thermally treated state, a brittle layer which is provided with numerous cracks, both transversely and longitudinally to the coating. ( Figure 10 compared to the aforementioned example of the invention (left in the picture)).
- a sheet, as in the aforementioned example, is heat-treated immediately after hot-dip galvanizing at about 490 ° C to 550 ° C with the zinc layer only partially converted to Zn-Fe phases.
- the process is carried out in such a way that the phase transformation is only partially carried out and therefore not yet converted zinc with aluminum on the surface is present and thus free aluminum as oxidation protection for the zinc layer is available.
- a 1 mm thick steel sheet is rapidly inductively heated to 900 ° C with the inventive heat-treated and only partially converted into Zn-Fe phase coating.
- the result is a surface that is gray and without defects.
- a SEM / EDX investigation of the cross section shows an approximately 20 ⁇ m thick surface layer, whereby from the originally approximately 15 ⁇ m thick zinc coating of the coating, an approximately 20 ⁇ m Zn-Fe layer has formed during inductive annealing due to diffusion.
- this layer shows the typical for the invention two-phase structure with a "leopard pattern", with a dark in the appearing phase with a composition Zn / Fe of about 30/70 and light areas with the composition Zn / Fe of about 80/20.
- a sheet is electrolytically galvanized by electrochemical deposition of zinc on steel. Upon annealing, the diffusion of the steel with the zinc layer produces a thin Zn-Fe layer. Most of the zinc oxidizes to zinc oxide, which appears green by the simultaneous formation of iron oxides. The surface shows a green appearance with local scale marks where the zinc oxide layer does not adhere to the steel.
- a SEM / EDX examination (FIG. 15) of the sample sheet in transverse section confirms that a large part of the coating consists of zinc-iron oxide deposits.
- the potential required for the current flow is included about +1 V and thus well above the steel potential.
- the potential fluctuates between +0.8 and -0.1 V, but is above the steel potential throughout the entire dissolution of the coating. It follows that the corrosion protection of a annealed, electrolytically galvanized sheet is a pure barrier protection, but which is less efficient than with fumed sheet, since the potential is lower at the beginning of the measurement with electrolytically coated sheet than with hot-dip aluminized sheet.
- the potential required for the dissolution lies above the steel potential throughout the entire dissolution.
- the potential-time diagram is shown in FIG. 16.
- the potential is fundamentally above steel potential, but varies in detail depending on the experiment under identical experimental conditions.
- a sheet is made by electroplating zinc and nickel on the steel surface.
- the weight ratio of zinc to nickel in the anticorrosion layer is about 90/10.
- the deposited layer thickness is 5 ⁇ m.
- the sheet is annealed with the coating for 4 minutes and 30 seconds at 900 ° C in the presence of atmospheric oxygen.
- the diffusion of the steel and the zinc layer creates a thin diffusion layer of zinc, nickel and iron.
- most of the zinc oxidizes again to zinc oxide.
- the surface shows a scaled, green appearance with small local flaking to which the oxide layer does not adhere to the steel.
- a SEM / EDX examination of a cross section (FIG. 17) shows that the majority of the coating has been oxidized and is thus not available for cathodic corrosion protection.
- the potential required for the resolution of the layer is 1.5 V, far above the steel potential. After approx. 250 seconds it sinks to approx. 0.04 V and oscillates between + 0.25 V. After approx. 1.700 seconds measuring time, it finally settles to a value of - 0.27 V and remains until the end of the Measurement at this value.
- the potential required for the resolution of the layer is well above the steel potential throughout the entire measurement time. Consequently, this coating has a pure barrier protection after annealing, without any cathodic corrosion protection (Figure 18).
- FIGS. 25 and 26 show the GDOES analyzes of the sheet coated according to Example 4 before and after annealing. Before hardening (FIG. 25), after about 15 ⁇ m, the zinc transition steel is transferred to the transition, after hardening the layer is about 23 ⁇ m thick.
- the cathodic corrosion protection is negligible with a voltage difference of 100 mV to the steel potential in poorly conducting electrolytes.
- a smaller difference to the steel potential is in principle still a cathodic corrosion protection, if a current flow is detected when using a steel electrode, but this is negligible for practical aspects, since the corrosive medium must conduct very well, so this contribution to the cathodic corrosion protection can be used.
- the area between the potential curve at the galvanostatic dissolution and the specified threshold value of 100 mV was set below the steel potential (FIG. 20). Only the area below the threshold is taken into account. The overlying surface contributes negligibly little or no cathodic corrosion protection and is therefore not included in the evaluation.
- the area thus obtained is multiplied by the current density, the protection energy per unit area with which the base material can be actively protected against corrosion. The greater this energy, the better the cathodic corrosion protection.
- the determined protective energies per unit area are compared with one another. While a sheet with the known aluminum-zinc layer of 55% aluminum and 44% zinc, as it is also known from the prior art, only a protection energy per unit area of about 1.8 J / cm 2 , which is Protection energy per unit area in accordance with the invention coated sheets 5.6 J / cm 2 and 5, 9 J / cm 2 .
- cathodic corrosion protection in the context of the invention, it is subsequently specified that coatings of 15 ⁇ m thickness are used and the illustrated process and experimental conditions at least a cathodic corrosion protection energy of 4 J / cm 2 is present.
- a zinc layer which has been deposited electrolytically on the steel sheet surface is not in itself capable of providing a corrosion protection according to the invention, even after a heating step above the austenitizing temperature.
- the invention can also be achieved with an electrodeposited coating.
- the zinc can be deposited simultaneously with the oxygen-affine elements or elements in an electrolysis step on the sheet surface, so that on the surface of the sheet a coating with a homogeneous structure is formed which contains both zinc and the or the oxygen-affine elements.
- a coating behaves like a coating of the same composition applied to the sheet surface in the hot-dip galvanizing process.
- a zinc layer is deposited on the sheet surface and in a second electrolysis step, the oxygen-affine element (s) is deposited on the zinc layer.
- the second coating of the oxygen-affine elements may be significantly thinner than the zinc coating.
- the outer layer located on the zinc layer oxidizes from the oxygen-deficient element (s) and protects the underlying zinc with an oxide skin.
- the oxygen affinity element or elements are selected so that they do not evaporate from the zinc layer or are oxidized in a manner that does not leave a protective oxide skin.
- first a zinc layer is deposited electrolytically and then a layer of the oxygen or the oxygen elements is applied by vapor deposition or other suitable coating methods of non-electrolytic type.
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MXPA06000825A MXPA06000825A (es) | 2003-07-29 | 2004-06-09 | Metodo para producir una pieza de acero endurecido. |
BRPI0412601 BRPI0412601B1 (pt) | 2003-07-29 | 2004-06-09 | método para produção de uma peça de aço endurecido |
CA 2533327 CA2533327C (en) | 2003-07-29 | 2004-06-09 | Method for producing a hardened steel part |
DE202004021264U DE202004021264U1 (de) | 2003-07-29 | 2004-06-09 | Korrosionsschicht und gehärtetes Stahlbauteil |
US10/566,059 US8021497B2 (en) | 2003-07-29 | 2004-06-09 | Method for producing a hardened steel part |
ES04739755.9T ES2525731T3 (es) | 2003-07-29 | 2004-06-09 | Procedimiento para la producción de un componente de acero templado |
CN200480022188.4A CN1829817B (zh) | 2003-07-29 | 2004-06-09 | 制造硬化钢零件的方法 |
JP2006521403A JP5113385B2 (ja) | 2003-07-29 | 2004-06-09 | 焼入れ鋼部品の製造方法 |
EP04739755.9A EP1658390B1 (de) | 2003-07-29 | 2004-06-09 | Verfahren zum herstellen eines gehärteten stahlbauteils |
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AT12022003A AT412403B (de) | 2003-07-29 | 2003-07-29 | Korrosionsgeschütztes stahlblech |
AT0120303A AT412878B (de) | 2003-07-29 | 2003-07-29 | Korrosionsgeschütztes stahlblechteil mit hoher festigkeit |
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PCT/EP2004/006251 WO2005021822A1 (de) | 2003-07-29 | 2004-06-09 | Verfahren zum herstellen eines gehärteten stahlbauteils |
PCT/EP2004/006250 WO2005021820A1 (de) | 2003-07-29 | 2004-06-09 | Verfahren zum herstellen eines gehärteten profilbauteils |
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