US20080308192A1 - Hydroxysulfate Surface Treatment - Google Patents

Hydroxysulfate Surface Treatment Download PDF

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Publication number
US20080308192A1
US20080308192A1 US10/583,765 US58376504A US2008308192A1 US 20080308192 A1 US20080308192 A1 US 20080308192A1 US 58376504 A US58376504 A US 58376504A US 2008308192 A1 US2008308192 A1 US 2008308192A1
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United States
Prior art keywords
sheet
zinc
treatment solution
sulfate
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Prior art date
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Abandoned
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US10/583,765
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English (en)
Inventor
Alain Bello
Eric Jacqueson
Claude Arnoux
Jacques Petitjean
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ArcelorMittal France SA
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Arcelor France SA
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Assigned to ARCELOR FRANCE reassignment ARCELOR FRANCE ASSIGNMENT OF ASSIGNORS INTEREST (SEE DOCUMENT FOR DETAILS). Assignors: ARNOUX, CLAUDE, BELLO, ALAIN, JACQUESON, ERIC, PETITJEAN, JACQUES
Publication of US20080308192A1 publication Critical patent/US20080308192A1/en
Abandoned legal-status Critical Current

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    • CCHEMISTRY; METALLURGY
    • C23COATING 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
    • C23CCOATING 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
    • C23C22/00Chemical 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
    • C23C22/05Chemical 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
    • C23C22/68Chemical 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 solutions with pH between 6 and 8
    • BPERFORMING OPERATIONS; TRANSPORTING
    • B21MECHANICAL METAL-WORKING WITHOUT ESSENTIALLY REMOVING MATERIAL; PUNCHING METAL
    • B21DWORKING OR PROCESSING OF SHEET METAL OR METAL TUBES, RODS OR PROFILES WITHOUT ESSENTIALLY REMOVING MATERIAL; PUNCHING METAL
    • B21D22/00Shaping without cutting, by stamping, spinning, or deep-drawing
    • B21D22/20Deep-drawing
    • CCHEMISTRY; METALLURGY
    • C23COATING 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
    • C23CCOATING 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
    • C23C2/00Hot-dipping or immersion processes for applying the coating material in the molten state without affecting the shape; Apparatus therefor
    • C23C2/04Hot-dipping or immersion processes for applying the coating material in the molten state without affecting the shape; Apparatus therefor characterised by the coating material
    • C23C2/06Zinc or cadmium or alloys based thereon
    • CCHEMISTRY; METALLURGY
    • C23COATING 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
    • C23CCOATING 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
    • C23C2/00Hot-dipping or immersion processes for applying the coating material in the molten state without affecting the shape; Apparatus therefor
    • C23C2/26After-treatment
    • CCHEMISTRY; METALLURGY
    • C23COATING 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
    • C23CCOATING 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
    • C23C22/00Chemical 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
    • C23C22/05Chemical 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
    • C23C22/06Chemical 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
    • C23C22/48Chemical 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 not containing phosphates, hexavalent chromium compounds, fluorides or complex fluorides, molybdates, tungstates, vanadates or oxalates
    • C23C22/53Treatment of zinc or alloys based thereon
    • CCHEMISTRY; METALLURGY
    • C25ELECTROLYTIC OR ELECTROPHORETIC PROCESSES; APPARATUS THEREFOR
    • C25DPROCESSES FOR THE ELECTROLYTIC OR ELECTROPHORETIC PRODUCTION OF COATINGS; ELECTROFORMING; APPARATUS THEREFOR
    • C25D11/00Electrolytic coating by surface reaction, i.e. forming conversion layers
    • C25D11/02Anodisation
    • C25D11/34Anodisation of metals or alloys not provided for in groups C25D11/04 - C25D11/32
    • CCHEMISTRY; METALLURGY
    • C25ELECTROLYTIC OR ELECTROPHORETIC PROCESSES; APPARATUS THEREFOR
    • C25DPROCESSES FOR THE ELECTROLYTIC OR ELECTROPHORETIC PRODUCTION OF COATINGS; ELECTROFORMING; APPARATUS THEREFOR
    • C25D9/00Electrolytic coating other than with metals
    • C25D9/04Electrolytic coating other than with metals with inorganic materials
    • C25D9/06Electrolytic coating other than with metals with inorganic materials by anodic processes

Definitions

  • a film of lubricating oil is applied to its surface so as to facilitate the forming operation.
  • the oil deficiency in certain areas of the oil film due to the dewetting effect is also responsible for lesser temporary corrosion protection of the steel sheet while it is being stored.
  • the subject of the invention is the use of an aqueous treatment solution containing sulfate ions SO 4 2 ⁇ with a concentration of not less than 0.01 mol/l in order to treat the surface of a steel sheet treated on at least one of its sides with a metal coating based on zinc or its alloys, for the purpose of reducing the formation of metal powder or particles based on zinc or its alloys generated by the degradation of the coating while said sheet is being formed.
  • the use of a steel sheet coated with an almost pure zinc coating is preferred.
  • a layer forms on the surface of the sheet that is based on zinc hydroxysulfate and zinc sulfate and is both sufficiently thick and sufficiently adherent.
  • SO 4 2 ⁇ concentration is less than 0.01 mol/l, but it has also been found that too high a concentration does not substantially improve the rate of deposition and may even slightly reduce it.
  • the treatment solution is applied in a conventional manner, for example by dipping, by spraying or by coating, both on electrogalvanized sheet and on hot-dip galvanized sheet.
  • the conditions under which the treatment solution is applied to the surface of the sheet namely the temperature, the time during which the solution is in contact with the galvanized surface, the SO 4 2 ⁇ ion concentration and the Zn 2+ ion concentration, are adjusted so as to form a layer based on zinc hydroxysulfate and zinc sulfate, the sulfur content of which is not less than 0.5 mg/m 2 . This is because when the sulfur content is less than 0.5 mg/m 2 , the reduction in degradation of the coating is less substantial.
  • the time during which the treatment solution is in contact with the galvanized surface is between two seconds and two minutes and the temperature of the treatment solution is between 20 and 60° C.
  • the treatment solution used contains between 20 and 160 g/l of zinc sulfate heptahydrate, which corresponds to a Zn 2+ ion concentration and an SO 4 2 ⁇ ion concentration that lie between 0.07 and 0.55 mol/l.
  • zinc sulfate heptahydrate which corresponds to a Zn 2+ ion concentration and an SO 4 2 ⁇ ion concentration that lie between 0.07 and 0.55 mol/l.
  • the treatment solution contains an oxidizing agent for zinc, such as hydrogen peroxide.
  • This oxidizing agent may have a very pronounced sulfation/hydroxysulfation accelerator effect at low concentration. It has been found that the addition of only 0.03%, i.e. 8 ⁇ 10 ⁇ 3 mol/l of hydrogen peroxide, or of 2 ⁇ 10 ⁇ 4 mol/l of potassium permanganate, to the solution makes it possible for the rate of deposition to be doubled (approximately). However, it has been found that concentrations 100 times higher no longer allow this improvement in deposition rate to be obtained.
  • the layer deposited on the sheet is adherent.
  • the drying is adjusted in order to remove the residual liquid water from the deposit.
  • the aqueous treatment solution having an SO 4 2 ⁇ ion concentration of not less than 0.01 mol/l is applied under anodic polarization and the pH of the treatment solution is equal to 12 or higher, but less than 13.
  • the pH of the solution is less than 12, adherent hydroxysulfates are not formed on the surface to be treated. If the pH of the solution is equal to 13 or higher, the hydroxysulfate redissolves and/or decomposes into zinc hydroxides.
  • the thickness of the zinc hydroxysulfate/zinc sulfate-based layer deposited corresponds to more than 0.5 mg/m 2 of equivalent sulfur, preferably at least 3.5 mg/m 2 of equivalent sulfur.
  • the total deposited amount of hydroxysulfates and sulfates is not less than 0.5 mg/m 2 but not to exceed 30 mg/m 2 of equivalent sulfur, preferably to be between 3.5 and 27 mg/m 2 of equivalent sulfur.
  • the zinc needed to form the zinc hydroxysulfate/zinc sulfate-based deposit comes from the anodic dissolution of zinc under the effect of the polarization of the galvanized surface.
  • the applied charge density is preferably between 10 and 100 C/dm 2 of surface to be treated.
  • the zinc hydroxy-sulfate/zinc sulfate-based layer to be deposited under a high polarization current density, especially greater than 20 A/dm 2 , for example 200 A/dm 2 .
  • the deposition efficiency is very low and the amount of sulfur in the deposited layer does not make it possible to significantly reduce the degradation of the zinc coating on the sheet while it is being formed.
  • the temperature of the treatment solution is generally between 20° C. and 60° C.
  • the treatment is carried out at a temperature of 40° C. or higher, so as to increase the conductivity of the solution and to reduce the ohmic losses.
  • the coated surface is thoroughly rinsed with demineralized water. This rinsing step is important in order to remove the alkaline reactants at the surface of the deposit, reactants that might cause corrosion problems.
  • the subject of the invention is also a method of lubricating a steel sheet coated with a layer consisting of a metal coating based on zinc or its alloys, in which method:
  • the weight of lubricating oil film applied is preferably less than 0.9 g/m 2 and is more particularly between 0.2 and 0.5 g/m 2 , since such weights are sufficient to obtain excellent temporary corrosion protection and to avoid any risk of contamination of workshops and forming tools.
  • the subject of the invention is the use of an aqueous treatment solution comprising sulfate ions with a concentration of not less than 0.01 mol/l, in order to improve temporary corrosion protection of a steel sheet coated with a metal layer based on zinc or its alloys.
  • This aqueous treatment solution is applied to the steel sheet according to the embodiments described in the paragraphs relating to the use of an aqueous treatment solution containing sulfate ions for treating a galvanized steel sheet for the purpose of reducing degradation of the zinc coating while the sheet is being formed.
  • the reader may refer to the paragraphs relating thereto.
  • the inventors have shown that the temporary corrosion protection of a galvanized steel sheet firstly treated with a treatment solution according to the invention and then coated with an oil film is very much better than that of a galvanized steel sheet that has not been treated beforehand.
  • FIG. 1 illustrates the results of the friction tests carried out on various sheet test pieces treated according to the invention or untreated;
  • FIG. 2 illustrates the results of the hot/wet corrosion tests carried out on various sheet test pieces according to the invention or untreated.
  • Test pieces were cut from a steel sheet, of “aluminum-killed steel” grade and of ES quality, with a thickness of 0.7 mm and coated on each of its sides with a zinc coating produced by hot dipping in a zinc bath.
  • An aqueous treatment solution according to the invention obtained from 125 g/l of zinc sulfate heptahydrate ZnSO 4 ⁇ 7H 2 O was prepared.
  • this treatment solution was applied to some of the test pieces by spraying the treatment solution at a temperature of 40° C. After the sheet was in contact with the solution for a time of 3 to 4 s, the treated sheet was drained and then dried.
  • a lubricating oil film was then applied to the zinc hydroxysulfate/zinc sulfate-based layer formed on the surface of the galvanized steel sheet test pieces, said oil being either QUAKER 6130 oil (from Quaker) or FUCHS 4107S oil (from Fuchs), with a film weight of 1.5 g/m 2 .
  • test pieces that had not been pretreated with the treatment solution according to the invention were oiled, either with the QUAKER 6130 oil or with the FUCHS 4107S oil, again with a film weight of 1.5 g/m 2 .
  • test pieces were then subjected to a controlled deformation test by means of a press comprising a punch, a die and a blank holder, recreating in the laboratory the stresses undergone by the sheet during a drawing operation, especially in the die radii and/or in the retaining rings with which the drawing tools are equipped.
  • Various blank-holder clamping forces were applied to the test pieces undergoing the test.
  • test pieces of the two series were weighed before the oiling operation and then at the end of the test, after de-oiling, by means of a balance accurate to 0.0001 grams.
  • the measured difference in weight was normalized to a weight loss per square meter, taking into account the area affected by the friction during the simulation of drawing the test piece, which was identical for each of the test pieces.
  • the press was wiped so as to identify the zinc coating powder or particles lost by the test piece in the press.
  • the weight loss results of the test pieces after drawing and the identification of zinc powder and/or particles coming from the coating are given in Table 1.
  • the particles and/or powder are identified by a rating in the following manner, according to a scale ranging from 1 to 4, where:
  • Test pieces 1 cm 2 in area were cut from a steel sheet, of “aluminum-killed steel” grade and of ES quality, with a thickness of 0.7 mm and coated on each of its sides with a zinc coating produced by hot dipping in a zinc bath.
  • test pieces were treated with a treatment solution according to the invention, under the same conditions as those indicated in Example 1, so as to form a zinc hydroxysulfate/zinc sulfate-based layer.
  • a lubricating oil film (QUAKER 6130 oil) is then applied to this layer in amounts ranging between 0.25 and 2.5 g/m 2 .
  • test pieces were oiled in the same manner as previously, but without having been pretreated with the treatment solution according to the invention.
  • the tester was a flat-on-flat tribometer known per se.
  • the test pieces to be tested were clamped with a clamping force F c between two high-speed steel plates offering a bearing (or sliding) surface to the test pieces.
  • the friction coefficient N was measured while moving the test piece relative to the plates over a total travel D of 180 mm and at a speed of 10 nm/s, while progressively increasing the clamping force F c .
  • a curve showing the variation in friction coefficient as a function of the clamping force F c for different lubricating oil film weights can then be plotted (see FIG. 1 ).
  • Test pieces were cut from a steel sheet, of “aluminum-killed steel” grade and of ES quality, with a thickness of 0.7 mm and coated on each of its sides with a zinc coating produced by hot dipping in a zinc bath.
  • test pieces were treated with a treatment solution according to the invention, under the same conditions as those indicated in Example 1, so as to form a zinc hydroxysulfate/zinc sulfate-based layer.
  • a lubricating oil film (QUAKER 6130 oil) was then applied to this layer in weights ranging between 0.25 and 1.0 g/m 2 .
  • test pieces were oiled in the same manner as previously, but without having been pretreated with the treatment solution according to the invention.
  • the lubricating oils applied to the steel sheets coated with the zinc-based metal coating guaranteed corrosion protection during the period of time that elapsed between manufacture of the sheets and their processing, for example by drawing.
  • test pieces to be tested were placed in an environmental chamber corresponding to the DIN 50017 standard, which simulates the conditions for corrosion of the external turn of a coil of sheet or of an individual cut sheet during storage.
  • test pieces were suspended vertically.
  • a curve showing the variation in the percentage content of white rust as a function of the number of cycles for each of the test pieces tested can then be plotted (cf. FIG. 2 ).

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  • Chemical & Material Sciences (AREA)
  • Engineering & Computer Science (AREA)
  • Organic Chemistry (AREA)
  • Materials Engineering (AREA)
  • Metallurgy (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Mechanical Engineering (AREA)
  • General Chemical & Material Sciences (AREA)
  • Electrochemistry (AREA)
  • Inorganic Chemistry (AREA)
  • Chemical Treatment Of Metals (AREA)
  • Other Surface Treatments For Metallic Materials (AREA)
  • Coating With Molten Metal (AREA)
  • Electroplating Methods And Accessories (AREA)
  • Electroplating And Plating Baths Therefor (AREA)
US10/583,765 2003-12-24 2004-12-14 Hydroxysulfate Surface Treatment Abandoned US20080308192A1 (en)

Applications Claiming Priority (3)

Application Number Priority Date Filing Date Title
FR0315381 2003-12-24
FR0315381A FR2864552B1 (fr) 2003-12-24 2003-12-24 Traitement de surface par hydroxysulfate
PCT/FR2004/003208 WO2005071140A1 (fr) 2003-12-24 2004-12-14 Traitement de surface par hydroxysulfate

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US20080308192A1 true US20080308192A1 (en) 2008-12-18

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US10/583,765 Abandoned US20080308192A1 (en) 2003-12-24 2004-12-14 Hydroxysulfate Surface Treatment

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US (1) US20080308192A1 (ru)
EP (2) EP2450470A1 (ru)
JP (1) JP2007517135A (ru)
KR (1) KR101022683B1 (ru)
CN (1) CN1914354A (ru)
BR (1) BRPI0418188B1 (ru)
CA (1) CA2551492A1 (ru)
FR (1) FR2864552B1 (ru)
MX (1) MXPA06007253A (ru)
RU (1) RU2371516C2 (ru)
UA (1) UA89368C2 (ru)
WO (1) WO2005071140A1 (ru)
ZA (1) ZA200605133B (ru)

Cited By (12)

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Publication number Priority date Publication date Assignee Title
US20100255341A1 (en) * 2007-09-04 2010-10-07 Jfe Steel Corporation Zinc-based metal plated steel sheet
US20110226387A1 (en) * 2008-01-30 2011-09-22 Jfe Steel Corporation Galvanized steel sheet and method for manufacturing the same
WO2015197430A1 (en) * 2014-06-27 2015-12-30 Henkel Ag & Co. Kgaa Dry lubricant for zinc coated steel
WO2018178108A1 (en) 2017-03-30 2018-10-04 Tata Steel Ijmuiden B.V. Aqueous acidic composition for treating metal surfaces, treating method using this composition and use of treated metal surface
US10253386B2 (en) 2012-03-07 2019-04-09 Jfe Steel Corporation Steel sheet for hot press-forming, method for manufacturing the same, and method for producing hot press-formed parts using the same
WO2019073273A1 (en) * 2017-10-12 2019-04-18 Arcelormittal PROCESS FOR PROCESSING METAL SHEET AND METAL SHEET TREATED WITH THIS METHOD
WO2019073320A1 (en) * 2017-10-12 2019-04-18 Arcelormittal PROCESS FOR PROCESSING METAL SHEET AND METAL SHEET PROCESSED THEREBY
US10294558B2 (en) 2012-04-25 2019-05-21 Arcelormittal Investigacion Y Desarrollo, S.L. Method for producing a metal sheet having oiled Zn—Al—Mg coatings, and corresponding metal sheet
EP3643759A1 (de) 2018-10-26 2020-04-29 Henkel AG & Co. KGaA Polycarboxylat-beschichteter bandstahl und dessen verwendung zum tiefziehen
WO2020126518A1 (de) 2018-12-19 2020-06-25 Henkel Ag & Co. Kgaa Umformbeschichtungsmittel, mit diesem mittel beschichteter bandstahl und dessen verwendung in der herstellung von bauteilen durch umformen
US10704157B2 (en) 2012-01-10 2020-07-07 ArcelorMittal Investigación y Desarrollo, S.L. Solution for reducing the blackening or tarnishing of a metal sheet and metal sheet
US11078573B2 (en) * 2016-01-19 2021-08-03 Thyssenkrupp Ag Method for producing a steel product with a Zn coating and a tribologically active layer deposited on the coating, and a steel product produced according to said method

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WO2010070942A1 (ja) * 2008-12-16 2010-06-24 Jfeスチール株式会社 亜鉛系めっき鋼板およびその製造方法
JP5396921B2 (ja) * 2009-03-06 2014-01-22 Jfeスチール株式会社 溶融金属が表面に付着し難い亜鉛系めっき鋼板
JP4883240B1 (ja) 2010-08-04 2012-02-22 Jfeスチール株式会社 熱間プレス用鋼板およびそれを用いた熱間プレス部材の製造方法
JP5884151B2 (ja) * 2010-11-25 2016-03-15 Jfeスチール株式会社 熱間プレス用鋼板およびそれを用いた熱間プレス部材の製造方法
JP5928247B2 (ja) * 2012-08-27 2016-06-01 Jfeスチール株式会社 冷延鋼板およびその製造方法
DE102012109855B4 (de) * 2012-10-16 2015-07-23 Thyssenkrupp Steel Europe Ag Verfahren zum Herstellen eines mit einer metallischen Korrosionsschutzschicht beschichteten Stahlprodukts
ES2734456T3 (es) 2013-09-19 2019-12-10 Fuchs Petrolub Se Capa funcional inorgánica sobre acero galvanizado por inmersión en caliente como ayuda para la conformación
EP2995674B1 (de) * 2014-09-11 2020-07-15 thyssenkrupp AG Verwendung eines Sulfats sowie Verfahren zum Herstellen eines Stahlbauteils durch Umformen in einer Umformmaschine
US10738226B2 (en) 2016-01-13 2020-08-11 Sika Technology Ag Single-component thermosetting epoxy resin with improved adhesion

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JP2001329352A (ja) * 2000-05-19 2001-11-27 Sumitomo Metal Ind Ltd 摺動性に優れた合金化溶融亜鉛めっき鋼板
WO2002097151A1 (fr) * 2001-05-28 2002-12-05 Kawasaki Steel Corporation Plaque d'acier galvanise par alliage, presentant d'excellentes proprietes de glissement
JP3582511B2 (ja) * 2001-10-23 2004-10-27 住友金属工業株式会社 熱間プレス成形用表面処理鋼とその製造方法
EP1666624B1 (en) * 2003-08-29 2017-06-07 JFE Steel Corporation Hot dip zinc plated steel sheet and method for production thereof

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US6528182B1 (en) * 1998-09-15 2003-03-04 Sollac Zinc coated steel plates coated with a pre-lubricating hydroxysulphate layer and methods for obtaining same

Cited By (25)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US20100255341A1 (en) * 2007-09-04 2010-10-07 Jfe Steel Corporation Zinc-based metal plated steel sheet
US8221900B2 (en) 2007-09-04 2012-07-17 Jfe Steel Corporation Zinc-based metal plated steel sheet
US8623514B2 (en) 2007-09-04 2014-01-07 Jfe Steel Corporation Zinc-based metal plated steel sheet
USRE45821E1 (en) 2007-09-04 2015-12-22 Jfe Steel Corporation Zinc-based metal plated steel sheet
US20110226387A1 (en) * 2008-01-30 2011-09-22 Jfe Steel Corporation Galvanized steel sheet and method for manufacturing the same
US10704157B2 (en) 2012-01-10 2020-07-07 ArcelorMittal Investigación y Desarrollo, S.L. Solution for reducing the blackening or tarnishing of a metal sheet and metal sheet
US10253386B2 (en) 2012-03-07 2019-04-09 Jfe Steel Corporation Steel sheet for hot press-forming, method for manufacturing the same, and method for producing hot press-formed parts using the same
US10294558B2 (en) 2012-04-25 2019-05-21 Arcelormittal Investigacion Y Desarrollo, S.L. Method for producing a metal sheet having oiled Zn—Al—Mg coatings, and corresponding metal sheet
US10865483B2 (en) 2012-04-25 2020-12-15 Arcelormittal Metal sheet having oiled Zn—Al—Mg coatings
US10287665B2 (en) 2014-06-27 2019-05-14 Henkel Ag & Co. Kgaa Dry lubricant for zinc coated steel
EP3161176B1 (en) 2014-06-27 2018-12-19 Henkel AG & Co. KGaA Dry lubricant for zinc coated steel
WO2015197430A1 (en) * 2014-06-27 2015-12-30 Henkel Ag & Co. Kgaa Dry lubricant for zinc coated steel
US11078573B2 (en) * 2016-01-19 2021-08-03 Thyssenkrupp Ag Method for producing a steel product with a Zn coating and a tribologically active layer deposited on the coating, and a steel product produced according to said method
WO2018178108A1 (en) 2017-03-30 2018-10-04 Tata Steel Ijmuiden B.V. Aqueous acidic composition for treating metal surfaces, treating method using this composition and use of treated metal surface
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WO2005071140A1 (fr) 2005-08-04
BRPI0418188A (pt) 2007-04-27
CN1914354A (zh) 2007-02-14
RU2371516C2 (ru) 2009-10-27
FR2864552B1 (fr) 2006-07-21
FR2864552A1 (fr) 2005-07-01
EP1699947A1 (fr) 2006-09-13
MXPA06007253A (es) 2006-08-18
CA2551492A1 (en) 2005-08-04
KR20060129306A (ko) 2006-12-15
ZA200605133B (en) 2007-09-26
UA89368C2 (ru) 2010-01-25
BRPI0418188B1 (pt) 2015-08-18
EP2450470A1 (fr) 2012-05-09
JP2007517135A (ja) 2007-06-28
KR101022683B1 (ko) 2011-03-17

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