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
  • C23C2/04—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

Definitions

• the present invention relates to a method for successively producing steel sheet coated with an iron-zinc alloy and conventional galvanized steel sheet in one and the same continuous galvanizing line without interrupting the operation of this line, along which a quantity of steel sheet coated with an iron-zinc alloy is produced by passing steel sheet through a bath of aluminiferous zinc containing less than about 0.15% by weight of aluminum and by subjecting the zinc-coated sheet thus obtained to a diffusion heat treatment so as to convert the layer of zinc present on the sheet into a zinc-iron alloy, and then we proceed directly to the production of a quantity of sheet conventional galvanized steel by bringing the aluminum content of the bath to more than about 0.15%, continuing to pass sheet steel through the bath and eliminating the heat treatment of diffusion.
• a bath consisting of zinc and 0.10% - ⁇ 0.15% by weight of aluminum is most often used, or a bath consisting of zinc and > 0.15-0.20% by weight of aluminum.
• the first type of bath is used when the zinc-coated sheet is subjected, after spinning the coating, to a diffusion heat treatment so as to transform the zinc coating into a coating of an iron-zinc alloy, what is commonly called "galvannealing".
• the second type of bath is used to produce conventional galvanized, that is to say sheet coated with a thin layer of zinc.
• the bath contains less than 0.12% aluminum, a whole range of iron-zinc compounds is formed at the interface between iron and zinc as described in the zinc-iron phase diagram, which should be avoided in the production of conventional galvanized.
• aluminum must in fact be greater than 0.15%. It's here this is why the second type of bath has an aluminum content of more than 0.15%.
• the first type of bath For an aluminum content of approximately 0.15%, a very thin layer of Fe 2 Al 5 alloy is formed on the surface of the steel which will block any subsequent diffusion. This is the reason why the first type of bath has an aluminum content of less than 0.15%.
• This first type of bath requires the presence of at least about 0.10% aluminum to slow the reaction between iron and zinc during the passage of the sheet in the bath; otherwise this reaction would result in excessive growth of the coating in the bath.
• the reaction between iron and zinc Although slowed down by aluminum, the reaction between iron and zinc nevertheless causes the formation of iron-zinc mattes which accumulate at the bottom of the bath and which are therefore called bottom mattes. These base mattes cease to be formed as soon as the aluminum content exceeds 0.15%; they therefore do not form in the second type of bath.
• part of the aluminum reacts with the iron in the sheet to form Fe 2 Al 5 compounds commonly known as floating mattes.
• This known process has the disadvantage that due to the increase in the aluminum content of the bath when switching from the first to the second type of bath, the iron-zinc mattes which are at this time in the bath, will gradually transform into floating iron-aluminum mattes, go back up and create defects on the sheet metal which passes in the bath; there is thus a risk of producing a e quantity substantial of lower quality sheet metal every time one goes from the production of "galvannealed" sheet to the production of conventional galvanized sheet.
• the object of the present invention is to provide a method as defined above, which avoids the drawback of this known method.
• a bath consisting of zinc, aluminum and silicon is used as the bath of aluminiferous zinc, the silicon content ranging from 0.005% to saturation and the aluminum content being at least 0.05% during the production of the steel sheet coated with an iron-zinc alloy and at most 0.5% during the production of the conventional galvanized steel sheet.
• documents JP-A-4218655 and JP-A-4235266 describe a process for the production of "galvannealed" sheet, in which use is made of a bath consisting of Zn, 0.001-0.2% Si and 0.05-0.20% Al, because silicon and aluminum would improve the machinability of the sheet. Since the bath used corresponds to that used in the process of the present invention, there should be no formation of bottom mat in this known process; however, this fact is not mentioned in these documents.
• the aluminum content must be at least 0.05% during the production of "galvannealed" sheet, because there is a risk of forming too thick coatings at lower contents. . It should not exceed 0.5% during the production of conventional galvanized sheet, because otherwise there is a risk of causing defects in the continuity of the coating.
• a silicon content of at least 0.005% is required to avoid the formation of background and aluminum mattes. The bath cannot be supersaturated with silicon, because a supersaturated bath can lead to coating defects.
• the bath contains at least 0.10% aluminum during the production of "galvannealed" sheet. It is also desirable that the bath contains at least 0.01% and at most 0.10% silicon.
• compositions can be used at temperatures from 430 to 510 ° C., that is to say at the temperatures which are normally used in continuous galvanizing. It may however be useful to operate at higher temperatures with the compositions containing more than 0.06% of silicon. Needless to say, the compositions having up to 0.14% Al will be used during the production of "galvannealed" sheet and that those having at least 0.16% Al will be used during the production of conventional galvanized.
• a bath consisting of zinc, aluminum and silicon used in this application, it is meant a bath which contains only these three metals, the impurities inevitably present in these metals and the impurities introduced into the bath by the passage of the sheet.
• well-known techniques can be used. , for example to the techniques described in the chapter “Continuous galvanizing and aluminizing” in “Engineering techniques”, M 1525, 1-13.

Landscapes

• Chemical & Material Sciences (AREA)
• Organic Chemistry (AREA)
• Materials Engineering (AREA)
• Mechanical Engineering (AREA)
• Metallurgy (AREA)
• Chemical Kinetics & Catalysis (AREA)
• Engineering & Computer Science (AREA)
• Coating With Molten Metal (AREA)
• Manufacture Of Alloys Or Alloy Compounds (AREA)
• Pyrane Compounds (AREA)
• Manufacturing Of Magnetic Record Carriers (AREA)
• Inorganic Insulating Materials (AREA)
• Superconductors And Manufacturing Methods Therefor (AREA)
• Electroplating And Plating Baths Therefor (AREA)
• Electroplating Methods And Accessories (AREA)

Applications Claiming Priority (3)

Publications (2)

Family

ID=9434478

Family Applications (1)

Country Status (17)

Families Citing this family (3)

Family Cites Families (10)

• 1992
  • 1992-10-13 FR FR9212213A patent/FR2696758B1/fr not_active Expired - Fee Related
• 1993
  • 1993-10-08 BR BR9307186A patent/BR9307186A/pt not_active IP Right Cessation
  • 1993-10-08 US US08/934,897 patent/US5882733A/en not_active Expired - Fee Related
  • 1993-10-08 SK SK410-95A patent/SK282049B6/sk unknown
  • 1993-10-08 WO PCT/EP1993/002754 patent/WO1994009173A1/fr not_active Ceased
  • 1993-10-08 AU AU51498/93A patent/AU688281B2/en not_active Ceased
  • 1993-10-08 AT AT93922530T patent/ATE141339T1/de not_active IP Right Cessation
  • 1993-10-08 CA CA002144963A patent/CA2144963A1/fr not_active Abandoned
  • 1993-10-08 DE DE69304079T patent/DE69304079T2/de not_active Expired - Fee Related
  • 1993-10-08 ES ES93922530T patent/ES2092837T3/es not_active Expired - Lifetime
  • 1993-10-08 RU RU95112581A patent/RU2114930C1/ru active
  • 1993-10-08 PL PL93308269A patent/PL172723B1/pl unknown
  • 1993-10-08 EP EP93922530A patent/EP0664838B1/de not_active Expired - Lifetime
  • 1993-10-08 JP JP6509587A patent/JPH08502098A/ja active Pending
  • 1993-10-08 HU HU9501070A patent/HU216338B/hu not_active IP Right Cessation
• 1995
  • 1995-04-10 FI FI951700A patent/FI100475B/fi active
• 1996
  • 1996-11-05 GR GR960402909T patent/GR3021535T3/el unknown

Non-Patent Citations (4)

Also Published As

Similar Documents

Legal Events