EP1482074A1 - Oberflächenbehandeltes stahlblech und verfahren zu seiner herstellung - Google Patents

Oberflächenbehandeltes stahlblech und verfahren zu seiner herstellung Download PDF

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Publication number
EP1482074A1
EP1482074A1 EP02705083A EP02705083A EP1482074A1 EP 1482074 A1 EP1482074 A1 EP 1482074A1 EP 02705083 A EP02705083 A EP 02705083A EP 02705083 A EP02705083 A EP 02705083A EP 1482074 A1 EP1482074 A1 EP 1482074A1
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Prior art keywords
steel sheet
coated steel
composite oxide
oxide film
film
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Application number
EP02705083A
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English (en)
French (fr)
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EP1482074A4 (de
Inventor
T. c/oI.P.DP. JFE Steel Corporation MIYOSHI
S. c/oI.P.Dp. JFE Steel Corporation ANDO
A. c/oI.P.Dp. JFE Steel Corporation MATSUZAKI
N. c/oIP Dp. JFE Steel Corporation YOSHIMI
T. c/oI.P.Dp. JFE Steel Corporation KUBATA
M. c/o I.P. Dp. JFE Steel Corporation YAMASHITA
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JFE Steel Corp
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JFE Steel Corp
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Publication of EP1482074A1 publication Critical patent/EP1482074A1/de
Publication of EP1482074A4 publication Critical patent/EP1482074A4/de
Withdrawn legal-status Critical Current

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    • C—CHEMISTRY; METALLURGY
    • C23—COATING METALLIC MATERIAL; COATING MATERIAL WITH METALLIC MATERIAL; CHEMICAL SURFACE TREATMENT; DIFFUSION TREATMENT OF METALLIC MATERIAL; COATING BY VACUUM EVAPORATION, BY SPUTTERING, BY ION IMPLANTATION OR BY CHEMICAL VAPOUR DEPOSITION, IN GENERAL; INHIBITING CORROSION OF METALLIC MATERIAL OR INCRUSTATION IN GENERAL
    • C23C—COATING METALLIC MATERIAL; COATING MATERIAL WITH METALLIC MATERIAL; SURFACE TREATMENT OF METALLIC MATERIAL BY DIFFUSION INTO THE SURFACE, BY CHEMICAL CONVERSION OR SUBSTITUTION; COATING BY VACUUM EVAPORATION, BY SPUTTERING, BY ION IMPLANTATION OR BY CHEMICAL VAPOUR DEPOSITION, IN GENERAL
    • C23C22/00—Chemical surface treatment of metallic material by reaction of the surface with a reactive liquid, leaving reaction products of surface material in the coating, e.g. conversion coatings, passivation of metals
    • C23C22/05—Chemical surface treatment of metallic material by reaction of the surface with a reactive liquid, leaving reaction products of surface material in the coating, e.g. conversion coatings, passivation of metals using aqueous solutions
    • C23C22/06—Chemical surface treatment of metallic material by reaction of the surface with a reactive liquid, leaving reaction products of surface material in the coating, e.g. conversion coatings, passivation of metals using aqueous solutions using aqueous acidic solutions with pH less than 6
    • C23C22/07—Chemical surface treatment of metallic material by reaction of the surface with a reactive liquid, leaving reaction products of surface material in the coating, e.g. conversion coatings, passivation of metals using aqueous solutions using aqueous acidic solutions with pH less than 6 containing phosphates
    • C23C22/08—Orthophosphates
    • 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
    • C23C28/00—Coating for obtaining at least two superposed coatings either by methods not provided for in a single one of groups C23C2/00 - C23C26/00 or by combinations of methods provided for in subclasses C23C and C25C or C25D
    • 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
    • C23C28/00—Coating for obtaining at least two superposed coatings either by methods not provided for in a single one of groups C23C2/00 - C23C26/00 or by combinations of methods provided for in subclasses C23C and C25C or C25D
    • C23C28/30—Coatings combining at least one metallic layer and at least one inorganic non-metallic layer
    • C23C28/32—Coatings combining at least one metallic layer and at least one inorganic non-metallic layer including at least one pure metallic layer
    • C23C28/322—Coatings combining at least one metallic layer and at least one inorganic non-metallic layer including at least one pure metallic layer only coatings of metal elements only
    • C23C28/3225—Coatings combining at least one metallic layer and at least one inorganic non-metallic layer including at least one pure metallic layer only coatings of metal elements only with at least one zinc-based layer
    • 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
    • C23C28/00—Coating for obtaining at least two superposed coatings either by methods not provided for in a single one of groups C23C2/00 - C23C26/00 or by combinations of methods provided for in subclasses C23C and C25C or C25D
    • C23C28/30—Coatings combining at least one metallic layer and at least one inorganic non-metallic layer
    • C23C28/34—Coatings combining at least one metallic layer and at least one inorganic non-metallic layer including at least one inorganic non-metallic material layer, e.g. metal carbide, nitride, boride, silicide layer and their mixtures, enamels, phosphates and sulphates
    • C23C28/345—Coatings combining at least one metallic layer and at least one inorganic non-metallic layer including at least one inorganic non-metallic material layer, e.g. metal carbide, nitride, boride, silicide layer and their mixtures, enamels, phosphates and sulphates with at least one oxide layer
    • B—PERFORMING OPERATIONS; TRANSPORTING
    • B05—SPRAYING OR ATOMISING IN GENERAL; APPLYING FLUENT MATERIALS TO SURFACES, IN GENERAL
    • B05D—PROCESSES FOR APPLYING FLUENT MATERIALS TO SURFACES, IN GENERAL
    • B05D7/00—Processes, other than flocking, specially adapted for applying liquids or other fluent materials to particular surfaces or for applying particular liquids or other fluent materials
    • B05D7/50—Multilayers
    • B05D7/51—One specific pretreatment, e.g. phosphatation, chromatation, in combination with one specific coating

Definitions

  • the present invention relates to a coated steel sheet having excellent heat resistance and damage resistance at forming, applicable to various parts of automobiles, household electric appliances, and building materials, and also to a method for manufacturing thereof.
  • zinc-base coated steel sheets are used in wide fields including automobiles, household electric appliances, and building materials. Aiming to provide functions such as corrosion resistance and paintability, chromate coating is conventionally applied to the surface of the zinc-base coated steel sheets, and further a thin-film resin coating treatment or the like is given to the chromated surface to form a several micrometers thick of thin resin film thereon.
  • Those zinc-base coated steel sheets have no heat resistance, thus they raise problems of discoloration, smoke emission, reduction in corrosion resistance caused by heating thereof when they are exposed to high temperature environments such as peripheral sections of automobile engine-room, oven, electronic oven, shrink band on cathode-ray tube of TV, and adjacent portions to welded section.
  • high temperature environments such as peripheral sections of automobile engine-room, oven, electronic oven, shrink band on cathode-ray tube of TV, and adjacent portions to welded section.
  • the steel sheets raise problems of causing scarathes to degrade the appearance during forming thereof caused by very thin film, and of degrading the corrosion resistance at the damaged section, though the discoloration is suppressed to some extent during heating thereof owing to the absence of organic component.
  • JP-A-4-33844 (the term "JP-A” referred to herein signifies "Japanese Patent Laid-Open Publication", (2) JP-A-6-179981, and (3) JP-A-7-278837.
  • the chromate coating uses hexavalent chromium which is classified as a regulated substance against pollution, contamination of environment and human body by the hexavalent chromium does substantially not occur because the treatment process is carried out in a closed system in which the hexavalent chromium is completely recovered and is not emitted to environment and because the elution of the hexavalent chromium from the chromate film is almost zero owing to the sealing action of organic composite film. Nevertheless, recent global environmental concern has enhanced the autonomous actions to decrease the use of heavy metals including hexavalent chromium. In addition, to prevent pollution of environment when shredder dust as a wasted product is disposed, action to zero or decrease the quantity of heavy metals in the products has appeared.
  • non-pollution treatment technologies not using chromate coating aiming to prevent the generation of white rust on zinc-base coated steel sheets.
  • Those technologies include several methods that utilize organic-base compounds and organic resins. Examples of them are the following:
  • the chromate coating is given on a coated steel sheet, and further a treatment solution containing silicic acid as the base which is solubilized to water using an alkali metal oxide, (water glass), is applied thereon to form the upper layer, followed by drying the upper layer.
  • a treatment solution containing silicic acid as the base which is solubilized to water using an alkali metal oxide, (water glass)
  • the prior arts (1) and (2) left the alkali metal component in the upper layer, a problem of poor water resistance to result in poor corrosion resistance arises.
  • the prior art (2) uses only inorganic component, the lubrication property is poor, which raises a problem of poor damage resistance at forming.
  • the prior art (3) forms a chromate film prepared by adding silica to a Zn-Ni alloy plating. Sole addition of silica is difficult to suppress the discoloration during heating, and raises a drawback of poor damage resistance at forming.
  • the prior art (4) forms a rudder type silicone resin on a chemical conversion film formed on a zinc-base coated steel sheet.
  • the formed silicone resin has a network structure (as understandable from the name of "rudder type"), so the cured film becomes excessively hard, which raises problems of poor damage resistance at forming and of poor adhesiveness of the film during forming.
  • the prior art (5) satisfies both the heat resistance and the damage resistance.
  • the prior art (5) uses chromate (containing hexavalent chromium) to improve the corrosion resistance, thus the material is not a non-pollutant material.
  • the prior arts (1) through (7) that do not use chromate use organic component as the main component. Accordingly, when these materials are heated to high temperatures, the organic component is thermally decomposed to fail in attaining sufficient corrosion resistance, and further the material surface blackens, thus fails to use as a heat-resistant material.
  • the inventors of the present invention found a zinc-base coated steel sheet that has excellent resistance to thermal discoloration, resistance to smoke emission under heating, corrosion resistance after heated, and damage resistance, by forming (1) a composite oxide film containing oxide fine particles and phosphoric acid-base compounds as the first layer, and (2) a resin film as the second layer, containing a specific straight silicone resin as the main component, on the surface of the zinc-base coated steel sheet.
  • Fig. 1 shows a'schematic front view of a testing apparatus for evaluating the damage resistance of test material.
  • a composite oxide film is formed as the first layer on the surface of a zinc-base coated steel sheet.
  • the composite oxide film according to the present invention contains ( ⁇ ) oxide fine particles and ( ⁇ ) phosphoric acid and/or phosphoric acid compound as the structuring components, and, if necessary, further contains ( ⁇ ) at least one element selected from the group consisting of Mg, Ca, Sr, Li, Mn, Fe, Co, Ni, Zn, Al, La, and Ce.
  • silicon dioxide is preferred.
  • Applicable silicon dioxide includes colloidal silica such as: Snowtex 0, OS, OXS, OUP, AK, 040, OL, and OZL, (acidic solutions), Snowtex XS, S, NXS, NS, N, OAS-25, LSS-35, LSS-45, and LSS-75, (alkaline solutions), produced by Nissan Chemical Industries, Ltd.
  • the ones having 14 nm or finer particle size are preferred, and further fine ones having 8 nm or smaller particle size are more preferred from the point of corrosion resistance.
  • a film composition solution containing dispersed dry-silica fine particles is applicable.
  • Preferred dry-silica includes AEROSIL 200, 300, 300CF, and 380 produced by Nippon Aerosil Co., Ltd., and the ones having 12 nm or smaller particle size are preferable, and the ones having 7 nm or smaller particle size are more preferable.
  • colloidal solution of fine particles of aluminum oxide, zirconium oxide, titanium oxide, cerium oxide, and antimony oxide may be used.
  • the ( ⁇ ) phosphoric acid and/or phosphoric acid compound which is a structural component of the composite oxide film
  • orthophosphoric acid, diphosphoric acid, polyphosphoric acid, metaphosphoric acid, or the like, and metallic salt or compound thereof may be added to the film composition as the film component.
  • primary phosphate is preferable from the point of stability of the film composition solution.
  • ammonium primary phosphate, ammonium secondary phosphate, or ammonium tertiary phosphate was added to the film composition solution, the corrosion resistance increased. Although the reason of increase in the corrosion resistance is not fully analyzed, use of these kinds of ammonium salt does not induce gelling of the solution even when the pH value of the film composition solution is increased. Since metallic salts generally become insoluble in alkaline domain, when a film is formed from a composition solution having high pH value, a compound more difficult in dissolving is presumably formed during the drying step.
  • Mn and Al are superior in corrosion resistance to other ( ⁇ ) components.
  • hydroxide is easily generated in neutral pH domain which is a corrosive environment, thus presumably forming a network for composite-forming together with phosphoric acid compound, silica, and the like to form a dense film.
  • Method for introducing the component ( ⁇ ) to the film is not specifically limited.
  • Phosphate, nitrate, sulfate, chloride, or the like of Mg, Ca, Sr, Li, Mn, Fe, Co, Ni, Zn, Al, La, and Ce may be added to the film composition solution.
  • a typical range of the coating weight of composite oxide film is, when the (a) oxide fine particles, above-described component ( ⁇ ) converted to P 2 O 5 , and above-described component ( ⁇ ) exist, from 5 to 4000 mg/m 2 , preferably from 50 to 1000 mg/m 2 , more preferably from 100 to 500 mg/m 2 , and most preferably from 200 to 400 mg/m 2 . If the coating weight thereof is smaller than 5 mg/m 2 , the corrosion resistance becomes not sufficient. If the coating weight exceeds 4000 mg/m 2 , the coating appearance and the appearance after heated degrade, and the electric conductivity decreases, which degrades the weldability and other characteristics.
  • the component (a) in the composite oxide film is silicon dioxide and that the coating weight of the silicon dioxide converted to SiO 2 is in a range of from 5 to 95 wt% as the mass ratio to the total coating weight of the composite oxide film defined before, preferably from 10 to 60 wt%.
  • the reason to attain particularly high corrosion resistance when the ratio of the phosphoric acid component to the metallic component is within the above-given range is not fully analyzed. Presumable reason of attaining the high corrosion resistance is that, since the solubility of phosphoric acid component varies with the ratio of the phosphoric acid to the-metal, the solubility of the film becomes particularly insoluble within the above-given range of the ratio of phosphoric acid to metallic component, which results in stronger barrier property of the film.
  • the film composition may further contain an additive of controlling the corrosion resistance.
  • an additive of controlling the corrosion resistance examples include polyphosphate and phosphate (such as zinc phosphate, ammonium dihydrogen phosphate, and zinc phosphite), molybdate, phosphomolybdate (such as aluminum phosphomolybdate), organic phosphoric acid and salt thereof (such as phytic acid, phytate, phosphonic acid, phosphonate, and their metallic salt and alkali metal salt), and organic inhibitor (such as hydrazine derivative, thiol compound, dithiocarbamate).
  • coupling agent such as silane coupling agent and titanium coupling agent
  • addition of organic resin and the like is not preferable because that kind of additive induces smoke emission and degradation in appearance when the material is heated to high temperatures.
  • the coated steel sheet according to the present invention has a film formed by applying a treatment solution as the second layer containing specified straight silicone resin as the main component onto the above-described first layer, followed by baking thereof.
  • a treatment solution as the second layer containing specified straight silicone resin as the main component onto the above-described first layer, followed by baking thereof.
  • silicone is a generic name of base materials having siloxane (-Si-O-Si-) portion therein, and generally resin, oil, rubber, and the like are used as the silicone.
  • the base material of that type of resin has a skeleton of siloxane (-Si-O-Si-), has silicon atoms binding with hydroxyl group (-OH), alkoxyl group (-OR: R designates an organic group), and organic group, and has both of organic property and inorganic property, while receiving no modification with other organic resin. Furthermore, the straight silicone resin has no bridge structure so that the resin is elastic in the film shape and has excellent damage resistance.
  • the applicable straight silicone resin may contain one of these organic groups or may contain two or more thereof. When a modified silicone resin, not the straight silicone resin, is used, the modified organic resin component thermally decomposes during the heating step to induce discoloration and smoke emission, so the use of modified silicone resin is not preferable.
  • methyl group which has smaller number of carbons is more preferable from the point of prevention of smoke emission caused by the decomposition of organic component under heating.
  • the content of SiO 2 component in the straight silicone resin is preferably 60% or more to the total film mass.
  • the preferable range is specified because components other than SiO 2 in the straight silicone resin are hydroxyl group or organic group so that the increase in the content of organic group degrades the smoke emission preventive property.
  • the reason to add an organic-base lubricant to the above-described silicone resin film is that the organic-base lubricant has a function to further effectively prevent the flaw and the galling on the resin film and the coating surface caused by roll-forming, press-forming, and the like.
  • the reason to adopt the organic-base lubricant having 70 °C or higher softening point is that below 70 °C of softening point is not preferable because of easy decomposition of organic component to degrade the prevention of smoke emission.
  • Examples of applicable organic-base lubricant having 70°C or higher softening point are MICROSTALIN WAX (70-90 °C of softening point), polyethylene (90-140 °C of softening point), polypropylene (140-170 °C of softening point), and tetrafluoroethylene (320 °C of softening point).
  • the above-described lubricants may be added separately or may be used two or more thereof.
  • the acid value of MICROSTALIN WAX, polyethylene, and polypropylene may be zero or more than zero, and their combined use may be applied.
  • the silicone resin is a solvent system
  • the adding state of the lubricant is preferably in powder form or in a state of dispersed in a solvent in advance.
  • the particle size of the lubricant is preferably 20 ⁇ m or smaller in view of damage resistance.
  • the crystalline lubricant of inorganic-base one including graphite, boron nitride, and molybdenum disulfide may be applied.
  • those kinds of inorganic-base lubricants are preferably used. They are, however, inferior in the damage resistance to the organic-base lubricants so that the use of inorganic-base lubricant may be adequately selected depending on the use objectives.
  • a preferable adding quantity of the organic-base lubricant is 20 parts by mass or less to 100 parts by mass of the straight silicone resin. If the added quantity of the organic-base lubricant exceeds 20 parts by mass, the quantity of organic component increases to degrade the smoke emission resistance under heating, which is not preferable. From the point of smoke emission prevention, a preferred added quantity is 10 parts by mass or less. For the case of inorganic-base lubricant, adding quantity of more than 20 parts by mass is not preferable because the damage resistance degrades.
  • a preferred range of coating weight of the straight silicone resin is from 0.1 to 3 g/m 2 converted to SiO 2 .
  • the coating weight is below 0.1 g/m 2 , the damage resistance during roll-forming and press-forming degrades.
  • the coating weight exceeds 3 g/m 2 , the smoke emission prevention in heating and the adhesiveness during bending work degrade, which is not preferable.
  • the film is formed by applying a coating consisting mainly of above-described straight silicone resin onto the surface of the zinc-base coated steel sheet, followed by heating to dry the coating.
  • coated steel sheets on which above-described film is formed include: galvanized steel sheets prepared by electroplating, hot-dip coating, and vapor deposition coating; zinc alloy coated steel sheets containing zinc and one or more elements of nickel, iron, aluminum, cobalt, molybdenum, and the like; and composite coated steel sheets having a coating film containing silica, alumina, and the like.
  • a zinc-nickel alloy coated steel sheet and a zinc-55% aluminum alloy coated steel sheet which have high melting point of the coated metal are more preferable from the point of heat resistance.
  • hot-dip aluminum coated steel sheet, not the zinc-base coating, and cold-rolled steel sheet and hot-rolled steel sheet, having no plating film are also applicable.
  • the steel as the substrate of the zinc-base coated steel sheet is not specifically limited, and the steel coils or sheets having various kinds of compositions and surface roughness, or prepared by various rolling methods can be applied.
  • Formation of the composite oxide film and the resin film on the surface of the zinc-base coated steel sheet are conducted as follows.
  • the above-described composite oxide film composition treatment solution is applied onto the surface of the zinc-base coated steel sheet using known method such as roll coating, curtain flow coating, and spray coating.
  • Thus applied solution is dried by a known method using hot-air furnace, induction-heating furnace, or the like to form the composite oxide film.
  • the coating consisting mainly of above-described straight silicone resin is applied onto the surface of thus prepared composite oxide film using a known method to form a predetermined coating weight of film.
  • the zinc-base coated steel sheet on which the coating is applied is then heated to bake thereof to a temperature range of from 80 °C to 300 °C in a hot-air furnace or an induction-heating furnace to vaporize the solvent in the coating, thus to form the resin film.
  • the reason to specify the concentration of the treatment solution to above-given range is the following. If the content of phosphoric acid and/or phosphoric acid compound is below 0.001 mol/l converted to P 2 O 5 , the wanted coating weight cannot be attained, which is not preferable. If the content thereof exceeds 6.0 mol/l, the stability of the treatment solution degrades, which is also not preferable. If the content of oxide fine particles is below 0.001 mol/l, the wanted coating weight cannot be attained, which is not preferable. If the content thereof exceeds 3.0 mol/l, the stability of the treatment solution degrades, which is also not preferable.
  • the above-described baking temperature of the resin film should be in a range of from 80 °C to 300 °C. If the baking temperature is below 80 °C, the hardening of resin film becomes insufficient, which degrades the damage resistance during working, thus the temperature range is not preferable. If the baking temperature exceeds 300 °C, the hardening of resin film excessively proceeds to induce decomposition and vaporization of organic group in the straight silicone resin, which results in poor damage resistance, which is not preferable.
  • the first layer film-forming treatment solutions (film compositions) shown in Table 1 and Table 2 were prepared.
  • the second layer film-forming treatment solutions (coating compositions) shown in Tables 3 through 5 were prepared.
  • Respective first film-forming treatment solutions shown in Tables 1 and 2 were applied onto the surface of respective plated steel sheets using roll coater (while adjusting the coating weight by the wet-coating weight), which were then heated to dry to form the respective first layer films.
  • respective coating compositions consisting mainly of straight silicone resin, given in Tables 3 to 5 were applied onto the respective first layer films by roll coating method (while adjusting the coating weight by the wet-coating weight), which were then baked in an induction-heating furnace to the ultimate plate temperatures of from 60 °C to 400 °C, thus the test materials were prepared.
  • the coating weight of composite oxide of the first layer and the coating weight of resin film of the second layer are given on Tables 3 to 5.
  • Every test material was subjected to soaking for one hour, then the state of discoloration on the surface thereof was determined by a colorimeter.
  • the criterion of the evaluation is the following.
  • test specimens 70 mm x 150 mm was cut from each test material.
  • Each of the test specimens was subjected to salt spray test specified by JIS Z2371.
  • the criterion of the evaluation is the following.
  • test specimens 70 mm x 150 mm were cut from each test material which was preliminarily treated by heating to 600 °C of ultimate sheet temperature, followed by soaking for one hour.
  • Each of the test specimens was subjected to salt spray test specified by JIS Z2371. The area of generated red rust after 500 hours was visually determined. The criterion of the evaluation is the following.
  • the applied testing apparatus is given in Fig. 1 showing schematic front view thereof.
  • the testing apparatus has: a female die 1 which has a flat face and which is fixed to a side 2a of a box frame 2; a male die 4 which faces the female die 1 and which has a substantially horizontal projection 3 positioned at a specified height; and a hydraulic cylinder 5 which supports the male die 4 and drives the male die 4 horizontally toward the female die 1, and which is fixed to other side 2b of the frame 2.
  • the male die 4 is fixed to a rod 5a of the hydraulic cylinder 5 via a load cell 6.
  • the width of the projection 3 of the male die 4 is 10 mm, and the length of the tip thereof is 1 mm.
  • test material was vertically inserted into the gap between the female die 1 and the male die 4.
  • the test material 7 was compressed by the hydraulic cylinder 5 under 50 kgf (500 kgf/cm 2 ) of pressure. Then, the test material was pulled-out upward at a speed of 500 mm/min to the "arrow" direction. Visual observation was given to the portion slid during the pulling out action to evaluate the damages on the film and the plating at the portion.
  • the criterion of evaluation is the following.
  • the coated steel sheets according to the present invention have excellent resistance to thermal discoloration and resistance to smoke emission in environments exposed to high temperatures, and have excellent resistance to corrosion before and after heating without using chromium. Furthermore, the coated steel sheets according to the present invention show excellent resistance to flaw on the film and the coating surface, and excellent adhesiveness of the film on being worked to form various parts.

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  • Chemical & Material Sciences (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Engineering & Computer Science (AREA)
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  • Mechanical Engineering (AREA)
  • Metallurgy (AREA)
  • Organic Chemistry (AREA)
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EP02705083A 2002-03-06 2002-03-06 Oberflächenbehandeltes stahlblech und verfahren zu seiner herstellung Withdrawn EP1482074A4 (de)

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
PCT/JP2002/002052 WO2003074760A1 (en) 2000-09-07 2002-03-06 Surface treated steel sheet and method for production thereof

Publications (2)

Publication Number Publication Date
EP1482074A1 true EP1482074A1 (de) 2004-12-01
EP1482074A4 EP1482074A4 (de) 2005-06-15

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EP (1) EP1482074A4 (de)
KR (1) KR100608137B1 (de)
CN (1) CN1524133A (de)
WO (1) WO2003074760A1 (de)

Cited By (1)

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Publication number Priority date Publication date Assignee Title
US20180050367A1 (en) * 2015-03-31 2018-02-22 Nippon Steel & Sumitomo Metal Corporation Hot-dip zinc-based plated steel sheet

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* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JP4683582B2 (ja) * 2005-02-02 2011-05-18 日本パーカライジング株式会社 水系金属材料表面処理剤、表面処理方法及び表面処理金属材料
JP5205845B2 (ja) * 2007-07-31 2013-06-05 Ｊｆｅスチール株式会社 耐油ぬれ拡がり性に優れた表面処理鋼板
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