AU2001210565B2 - Zinc-based metal plated steel sheet treated with phosphate excellent in formability and method for producing the same - Google Patents
Zinc-based metal plated steel sheet treated with phosphate excellent in formability and method for producing the same Download PDFInfo
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- AU2001210565B2 AU2001210565B2 AU2001210565A AU2001210565A AU2001210565B2 AU 2001210565 B2 AU2001210565 B2 AU 2001210565B2 AU 2001210565 A AU2001210565 A AU 2001210565A AU 2001210565 A AU2001210565 A AU 2001210565A AU 2001210565 B2 AU2001210565 B2 AU 2001210565B2
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- phosphate
- steel sheet
- wax
- galvanized steel
- zinc
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- NBIIXXVUZAFLBC-UHFFFAOYSA-K phosphate Chemical compound [O-]P([O-])([O-])=O NBIIXXVUZAFLBC-UHFFFAOYSA-K 0.000 title claims description 56
- 229910019142 PO4 Inorganic materials 0.000 title claims description 50
- 239000010452 phosphate Substances 0.000 title claims description 50
- 238000004519 manufacturing process Methods 0.000 title claims description 7
- 229910000831 Steel Inorganic materials 0.000 title description 20
- 239000010959 steel Substances 0.000 title description 20
- 239000011701 zinc Substances 0.000 title description 11
- HCHKCACWOHOZIP-UHFFFAOYSA-N Zinc Chemical compound [Zn] HCHKCACWOHOZIP-UHFFFAOYSA-N 0.000 title description 6
- 229910052725 zinc Inorganic materials 0.000 title description 6
- 229910052751 metal Inorganic materials 0.000 title description 2
- 239000002184 metal Substances 0.000 title description 2
- 229910001335 Galvanized steel Inorganic materials 0.000 claims description 29
- 239000008397 galvanized steel Substances 0.000 claims description 29
- 229920000098 polyolefin Polymers 0.000 claims description 16
- 239000007864 aqueous solution Substances 0.000 claims description 12
- 229910021645 metal ion Inorganic materials 0.000 claims description 8
- 238000000034 method Methods 0.000 claims description 8
- 229910052749 magnesium Inorganic materials 0.000 claims description 3
- 239000010410 layer Substances 0.000 description 30
- 239000011248 coating agent Substances 0.000 description 26
- 238000000576 coating method Methods 0.000 description 26
- 230000000052 comparative effect Effects 0.000 description 12
- QQFLQYOOQVLGTQ-UHFFFAOYSA-L magnesium;dihydrogen phosphate Chemical compound [Mg+2].OP(O)([O-])=O.OP(O)([O-])=O QQFLQYOOQVLGTQ-UHFFFAOYSA-L 0.000 description 10
- 229910000401 monomagnesium phosphate Inorganic materials 0.000 description 10
- 235000019785 monomagnesium phosphate Nutrition 0.000 description 10
- VLKZOEOYAKHREP-UHFFFAOYSA-N n-Hexane Chemical compound CCCCCC VLKZOEOYAKHREP-UHFFFAOYSA-N 0.000 description 8
- LRXTYHSAJDENHV-UHFFFAOYSA-H zinc phosphate Chemical compound [Zn+2].[Zn+2].[Zn+2].[O-]P([O-])([O-])=O.[O-]P([O-])([O-])=O LRXTYHSAJDENHV-UHFFFAOYSA-H 0.000 description 8
- 229910000165 zinc phosphate Inorganic materials 0.000 description 8
- 238000005033 Fourier transform infrared spectroscopy Methods 0.000 description 6
- 239000011324 bead Substances 0.000 description 6
- 239000000243 solution Substances 0.000 description 6
- 239000002904 solvent Substances 0.000 description 6
- 239000000126 substance Substances 0.000 description 6
- 239000000203 mixture Substances 0.000 description 4
- 238000001878 scanning electron micrograph Methods 0.000 description 4
- 229910045601 alloy Inorganic materials 0.000 description 3
- 239000000956 alloy Substances 0.000 description 3
- 239000004566 building material Substances 0.000 description 3
- 239000013078 crystal Substances 0.000 description 3
- NBIIXXVUZAFLBC-UHFFFAOYSA-M dihydrogenphosphate Chemical compound OP(O)([O-])=O NBIIXXVUZAFLBC-UHFFFAOYSA-M 0.000 description 3
- 239000007787 solid Substances 0.000 description 3
- 238000011282 treatment Methods 0.000 description 3
- 239000004698 Polyethylene Substances 0.000 description 2
- 229910007567 Zn-Ni Inorganic materials 0.000 description 2
- 229910007614 Zn—Ni Inorganic materials 0.000 description 2
- 238000010521 absorption reaction Methods 0.000 description 2
- 230000015572 biosynthetic process Effects 0.000 description 2
- YYRMJZQKEFZXMX-UHFFFAOYSA-L calcium bis(dihydrogenphosphate) Chemical compound [Ca+2].OP(O)([O-])=O.OP(O)([O-])=O YYRMJZQKEFZXMX-UHFFFAOYSA-L 0.000 description 2
- 229940062672 calcium dihydrogen phosphate Drugs 0.000 description 2
- 229910000389 calcium phosphate Inorganic materials 0.000 description 2
- ZCDOYSPFYFSLEW-UHFFFAOYSA-N chromate(2-) Chemical compound [O-][Cr]([O-])(=O)=O ZCDOYSPFYFSLEW-UHFFFAOYSA-N 0.000 description 2
- 238000005260 corrosion Methods 0.000 description 2
- 230000007797 corrosion Effects 0.000 description 2
- 238000005336 cracking Methods 0.000 description 2
- NAAXGLXYRDSIRS-UHFFFAOYSA-L dihydrogen phosphate;manganese(2+) Chemical compound [Mn+2].OP(O)([O-])=O.OP(O)([O-])=O NAAXGLXYRDSIRS-UHFFFAOYSA-L 0.000 description 2
- 239000000839 emulsion Substances 0.000 description 2
- 229910052742 iron Inorganic materials 0.000 description 2
- JEIPFZHSYJVQDO-UHFFFAOYSA-N iron(III) oxide Inorganic materials O=[Fe]O[Fe]=O JEIPFZHSYJVQDO-UHFFFAOYSA-N 0.000 description 2
- 239000011777 magnesium Substances 0.000 description 2
- 229910052748 manganese Inorganic materials 0.000 description 2
- 239000011572 manganese Substances 0.000 description 2
- 235000019691 monocalcium phosphate Nutrition 0.000 description 2
- 238000007747 plating Methods 0.000 description 2
- -1 polyethylene Polymers 0.000 description 2
- 229920000573 polyethylene Polymers 0.000 description 2
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 2
- VYZAMTAEIAYCRO-UHFFFAOYSA-N Chromium Chemical compound [Cr] VYZAMTAEIAYCRO-UHFFFAOYSA-N 0.000 description 1
- 229910001297 Zn alloy Inorganic materials 0.000 description 1
- 230000002378 acidificating effect Effects 0.000 description 1
- 239000002390 adhesive tape Substances 0.000 description 1
- 229910052782 aluminium Inorganic materials 0.000 description 1
- XAGFODPZIPBFFR-UHFFFAOYSA-N aluminium Chemical compound [Al] XAGFODPZIPBFFR-UHFFFAOYSA-N 0.000 description 1
- 238000004458 analytical method Methods 0.000 description 1
- 229910052791 calcium Inorganic materials 0.000 description 1
- 239000011575 calcium Substances 0.000 description 1
- 125000002091 cationic group Chemical group 0.000 description 1
- 150000001768 cations Chemical class 0.000 description 1
- 229910052804 chromium Inorganic materials 0.000 description 1
- 239000011651 chromium Substances 0.000 description 1
- JOPOVCBBYLSVDA-UHFFFAOYSA-N chromium(6+) Chemical compound [Cr+6] JOPOVCBBYLSVDA-UHFFFAOYSA-N 0.000 description 1
- 239000011247 coating layer Substances 0.000 description 1
- 229910052802 copper Inorganic materials 0.000 description 1
- 239000010949 copper Substances 0.000 description 1
- 230000007423 decrease Effects 0.000 description 1
- 238000005238 degreasing Methods 0.000 description 1
- RGPUVZXXZFNFBF-UHFFFAOYSA-K diphosphonooxyalumanyl dihydrogen phosphate Chemical compound [Al+3].OP(O)([O-])=O.OP(O)([O-])=O.OP(O)([O-])=O RGPUVZXXZFNFBF-UHFFFAOYSA-K 0.000 description 1
- 238000001035 drying Methods 0.000 description 1
- 239000000428 dust Substances 0.000 description 1
- 238000004070 electrodeposition Methods 0.000 description 1
- 238000011156 evaluation Methods 0.000 description 1
- 239000000383 hazardous chemical Substances 0.000 description 1
- 238000007654 immersion Methods 0.000 description 1
- 229910052759 nickel Inorganic materials 0.000 description 1
- 239000002245 particle Substances 0.000 description 1
- 238000003825 pressing Methods 0.000 description 1
- 230000001105 regulatory effect Effects 0.000 description 1
- 238000000527 sonication Methods 0.000 description 1
- 238000005507 spraying Methods 0.000 description 1
Classifications
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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
-
- 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
- C23C22/73—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 characterised by the process
-
- C—CHEMISTRY; METALLURGY
- C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
- C10M—LUBRICATING COMPOSITIONS; USE OF CHEMICAL SUBSTANCES EITHER ALONE OR AS LUBRICATING INGREDIENTS IN A LUBRICATING COMPOSITION
- C10M101/00—Lubricating compositions characterised by the base-material being a mineral or fatty oil
- C10M101/02—Petroleum fractions
- C10M101/025—Petroleum fractions waxes
-
- C—CHEMISTRY; METALLURGY
- C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
- C10M—LUBRICATING COMPOSITIONS; USE OF CHEMICAL SUBSTANCES EITHER ALONE OR AS LUBRICATING INGREDIENTS IN A LUBRICATING COMPOSITION
- C10M173/00—Lubricating compositions containing more than 10% water
- C10M173/02—Lubricating compositions containing more than 10% water not containing mineral or fatty oils
-
- 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
- C23C22/82—After-treatment
- C23C22/83—Chemical after-treatment
-
- 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
- B05D7/14—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 to metal, e.g. car bodies
-
- 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
-
- C—CHEMISTRY; METALLURGY
- C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
- C10M—LUBRICATING COMPOSITIONS; USE OF CHEMICAL SUBSTANCES EITHER ALONE OR AS LUBRICATING INGREDIENTS IN A LUBRICATING COMPOSITION
- C10M2205/00—Organic macromolecular hydrocarbon compounds or fractions, whether or not modified by oxidation as ingredients in lubricant compositions
- C10M2205/14—Synthetic waxes, e.g. polythene waxes
-
- C—CHEMISTRY; METALLURGY
- C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
- C10M—LUBRICATING COMPOSITIONS; USE OF CHEMICAL SUBSTANCES EITHER ALONE OR AS LUBRICATING INGREDIENTS IN A LUBRICATING COMPOSITION
- C10M2205/00—Organic macromolecular hydrocarbon compounds or fractions, whether or not modified by oxidation as ingredients in lubricant compositions
- C10M2205/14—Synthetic waxes, e.g. polythene waxes
- C10M2205/143—Synthetic waxes, e.g. polythene waxes used as base material
-
- C—CHEMISTRY; METALLURGY
- C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
- C10N—INDEXING SCHEME ASSOCIATED WITH SUBCLASS C10M RELATING TO LUBRICATING COMPOSITIONS
- C10N2040/00—Specified use or application for which the lubricating composition is intended
- C10N2040/20—Metal working
- C10N2040/24—Metal working without essential removal of material, e.g. forming, gorging, drawing, pressing, stamping, rolling or extruding; Punching metal
-
- C—CHEMISTRY; METALLURGY
- C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
- C10N—INDEXING SCHEME ASSOCIATED WITH SUBCLASS C10M RELATING TO LUBRICATING COMPOSITIONS
- C10N2050/00—Form in which the lubricant is applied to the material being lubricated
- C10N2050/015—Dispersions of solid lubricants
- C10N2050/02—Dispersions of solid lubricants dissolved or suspended in a carrier which subsequently evaporates to leave a lubricant coating
-
- C—CHEMISTRY; METALLURGY
- C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
- C10N—INDEXING SCHEME ASSOCIATED WITH SUBCLASS C10M RELATING TO LUBRICATING COMPOSITIONS
- C10N2080/00—Special pretreatment of the material to be lubricated, e.g. phosphatising or chromatising of a metal
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- Chemical & Material Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- General Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Engineering & Computer Science (AREA)
- Oil, Petroleum & Natural Gas (AREA)
- Materials Engineering (AREA)
- Mechanical Engineering (AREA)
- Metallurgy (AREA)
- Chemical Treatment Of Metals (AREA)
Description
f,
DESCRIPTION
PHOSPHATE-TREATEDGALVANIZED STEEL SHEET WITH IMPROVED WORKABILITY AND PRODUCTION METHOD THEREOF TECHNICAL FIELD The present invention relates to galvanized steel sheets having improved workability that makes them suitable for use in applications such as automobiles, home electric appliances and building materials.
TECHNICAL BACKGROUND Galvanized steel sheets that are used in applications such as automobiles, home electric appliances, and building materials have often been treated with phosphate, chromate and organic coating prior to their use in order to impart desired properties such as corrosion resistance and workability, and to thereby improve their value. Since chromate-treated steel sheets may contain chromium (VI) and may be harmful to the environment, they have become less favored, and instead, demands are increasing for phosphate-treated steel sheets. On the other hand, Zn-Ni alloy-electrogalvanized steel sheets, now widely in use because of their highworkability, contain Ni and therefore lead to increased manufacturing costs.
For these reasons, attempts have been made to apply phosphate 1 treatments to less costly electrogalvanized steel sheets, hotdip galvanized steel sheets, or alloy hot-dip galvanized steel sheets to improve their value.
However, when Zn electrogalvanized steel sheets, hot-dip galvanized steel sheets, or alloy hot-dip galvanized steel sheets are treated with phosphate in a conventional manner, the resulting workability tends to be insufficient as compared to the workability attainable by Zn-Ni alloy-electrogalvanized steel sheets. This is particularly the case in an increasingly common application in which steel sheets are drawn while the amount of the steel sheet fed to a die is regulated by means of beading. In light of this, a zinc phosphate-treated galvanized steel sheet disclosed in Japanese Patent Laid-open Publication No. Hei 7-138764 contains at least one of Fe, Co, Ni, Ca, Mg and Mn and exhibits an improved pressability. Even this type of steel sheet fails to provide sufficient performance required in the aforementioned drawing process that takes advantage of beading.
DISCLOSURE OF THE INVENTION Accordingly, it is an objective of the present invention to provide a phosphate-treated galvanized steel sheet that has overcome the above-described drawbacks of the prior art and exhibits an improved workability.
In an effort to improve the workability of phosphate- 2 treated galvanized steel sheets, the present inventors have conceived of adding a wax to the phosphate coating. This has proven difficult, however, because of the manner by which conventional phosphate treatment is carried out: applying an acidic aqueous solution containing phosphate ions and metal cations to the galvanized surface either by spraying or by immersion in the solution. In this manner, the pH of the phosphate-treatment solution is increased on the galvanized surface, causing phosphate crystals to deposit on the surface.
The present inventors have also attempted to deposit a wax layer on top of the phosphate coating. This approach failed to provide necessary workability and coat adhesion due to insufficient fixation of the wax to the coating layer. In the search for a way to solve these:problems, the present inventors have discovered that a phosphate layer containing a polyolefin wax or a modified polyolefin wax can be obtained by first applying a phosphate coating onto the surface of a galvanized steel sheet using a known technique and subsequently applying and drying an aqueous solution containing the polyolefin wax or the modified polyolefin wax along with phosphate ions and polyvalent metal ions. The steel sheets manufactured in this manner achieve excellent workability. Collectively, these findings led the present inventors to devise the present invention.
Accordingly, one aspect of the present invention provides 3 a phosphate-treated galvanized steel sheet with improved workability having a phosphate layer deposited on the surface thereof. The steel sheet is characterized in that the phosphate layer contains a polyolefin wax or a modified polyolefin wax. Also provided is a method for producing such a phosphate-treated galvanized steel sheet. The method is characterized in that, following the application of phosphate onto the surface of the galvanized steel sheet, an aqueous solution containing a polyolefin wax or a modified polyolefin wax along with phosphate ions and polyvalent metal ions is applied over the phosphate layer and is then dried.
The galvanized steel sheet for use in the present invention may be a steel sheet plated either with pure zinc or a zinc alloy, which in each case serves to improve the workability of the steel sheet. Among different types of galvanization, Zn electrogalvanization, hot-dip galvanization, and alloy hot-dip galvanization are preferred in view of manufacturing costs.
Also, the phosphate coating applied over the zinc plating may be any phosphate coating although a zinc phosphate coating that forms "hopite crystals" or a zinc phosphate coating modified by Fe, Ni, Co, Mn, Mg, Ca, Cu and other elements are generally preferred.
It is essential that the aqueous solution to be applied over the phosphate layer deposited on top of the zinc plating 4 contain a polyolefin wax or a modified polyolefin wax, along with phosphate ions and polyvalent metal ions. The waxcontaining phosphate layer can be formed by applying the aqueous solution in which all of the above components coexist.
Preferably, the polyvalent metal ion is Mg2+, Mn2+, Ca2+, Zn"2, Ni 2 Co 2 or Al 3 These metal ions may be used either individually or as a mixture of two or more. Of these, Mg2+ or Mn2" is most preferred in view of corrosion-resistance.
It should be noted that a mixed aqueous solution of a polyolefin wax or a modified polyolefin wax (which may be referred to simply as "wax," hereinafter) and a dihydrogenphosphate is most convenient for the production of the galvanized steel sheet.
Examples of the dihydrogenphosphate include magnesium dihydrogenphosphate, aluminum dihydrogenphosphate, manganese dihydrogenphosphate, and calcium dihydrogenphosphate. Of these, magnesium dihydrogenphosphate is most preferred in view of corrosion resistance.
Preferably, the wax is either cationic or nonionic wax so that it can stably mix with phosphate ions and polyvalent metal ions.
While the wax may be added in any amount, it is preferably added in an amount of about 10% or less with respect to the total weight of the phosphate layer, considering the adhesion of the coating.
Figs. 1 and 2 each show a scanning electron micrography (SEM) of a wax-containing phosphate layer (15kV, X5000) made by the methods described below in Examples 1 and 2, respectively, whereas Fig. 3 shows a SEM image of a wax-free phosphate layer (15kV, X5000) made by the method described below in Comparative Example 2. The results of FT-IR spectroscopy (PERKIN-ELMER, high-sensitivity reflection) of respective samples are also shown in Fig. 4. Each layer was observed after sonicating each of the steel sheets in n-hexane solvent for 5 minutes. The comparison between Figs. 1, 2, and 3 reveals that each of the wax-containing phosphate layers of the present invention has a uniform, fine crystal structure similar to that of the typical wax-free phosphate layer. It is thus difficult to know from the surface appearance if a given layer contains the wax. In comparison, it is known from Fig. 4 that each of the wax-containing phosphate layers has absorption peaks at 2800 to 3000cm 1 indicative of C-H bonds present in the wax. Thus, by this approach, it can be determined if the layer contains the wax.
These peaks at 2800 to 3000cm-1 can also be detected by FT-IR when the wax alone is applied over the wax-free phosphate layer to form film over the phosphate layer. In this case, however, the peak intensity significantly decreases over time and the peaks eventually disappear as the phosphate layer is degreased in a solvent such as n-hexane. In this manner, 6 the wax-free phosphate layer with independently applied wax can be distinguished from the wax-containing phosphate layer of the present invention (Alternatively, with the solvent applied, the surface of a given layer may be rubbed to see if visible scratches will be formed on the surface. Scratches are hardly visible if the layer is the wax-containing phosphate layer of the present invention.). In addition,-wax layer independently applied to the wax-free phosphate layer is readily removed by the solvent component present in a typical wash oil and the steel sheet does not exhibit a high workability when the actual procedures for press are simulated wash oil applied before pressing). Furthermore, the wax-free phosphate layer tends to show a reduced coat adhesion and thus is not preferred.
If the surface of the layer is not completely degreased and the rust proof oil or dust particles remain on the surface, then the absorption at 2800 to 3000cm 1 may be observed for the wax-free phosphate layer in FT-IR analysis. Thus, the surface of the layer must be completely degreased prior to FT-IR using n-hexane or other solvents.
BRIEF DESCRIPTION OF THE DRAWINGS Fig. 1 is a SEM image (X5000) showing the surface of a galvanized steel sheet treated with a wax-containing phosphate in accordance with Example i.
Fig. 2 is a SEM image (X5000) showing the surface of another galvanized steel sheet treated with a wax-containing phosphate in accordance with Example 2.
Fig. 3 is a SEM image (X5000) showing the surface of another galvanized steel sheet treated with a wax-free phosphate in accordance with Comparative Example 2.
Fig. 4 is the result of FT-IR spectroscopy of the phosphate-treated galvanized steel sheets of Example 1, Example 2, and Comparative Example 2.
BEST MODE FOR CARRYING OUT THE INVENTION The present invention will now be described in detail with reference to Examples, which are not intended to limit the scope of the invention in any way.
In each of Examples and Comparative Examples, a 0.7mm thick electrogalvanized steel sheet that has an r-value (Lankford value) of 1.9 and has been plated to an amount of 2 (per one side) was used to make a sample sheet.
Example 1 A piece of the steel sheet was surface-conditioned (Pl-Zn manufactured by NIHON PARKERIZING Co., Ltd.) and was then treated with zinc phosphate (PB-3322 manufactured by NIHON PARKERIZING Co., Ltd.) to prepare a zinc phosphate-treated galvanized steel sheet with a coating amount of 0.7g/m 2 Meanwhile, an aqueous solution of magnesium dihydrogenphosphate (YONEYAMA CHEMICAL INDUSTRIES Co., Ltd.) and an emulsion of modified nonionic polyethylene wax (Chemicerac SH5200 manufactured by SANYO CHEMICAL INDUSTRIES Co., Ltd.) were mixed with each other so that the ratio of magnesium dihydrogenphosphate to wax in the resulting mixture was 100:5 as measured by the weight of solid content. Using a roll coater, the mixture was applied onto the zinc phosphatetreated galvanized steel sheet. The sheet was then dried while the temperature of the sheet was maintained at 100 0 C. The weight of the applied coating as determined by the difference between the weight of the sheet before coating and the weight of the sheet after coating was adjusted to 0.7g/m 2 Example 2 A sample sheet was prepared in the same manner as in Example 1, except that the ratio of magnesium dihydrogenphosphate to wax is 100:1 as measured by the weight of solid content.
Example 3 A sample sheet was prepared in the same manner as in Example 1, except that the ratio of magnesium dihydrogenphosphate to wax is 100:10 as measured by the weight of solid content.
Example 4 A sample sheet was prepared in the same manner as in Example 1, except that an aqueous solution of aluminum 9 dihydrogenphosphate (YONEYAMA CHEMICAL INDUSTRIES Co., Ltd.) was used in place of magnesium dihydrogenphosphate solution.
Example A sample sheet was prepared in the same manner as in Example 1, except that an aqueous solution of manganese dihydrogenphosphate.(YONEYAMA CHEMICAL INDUSTRIES Co., Ltd.) was used in place of magnesium dihydrogenphosphate solution.
Example 6 A sample sheet was prepared in the same manner as in Example 1, except that an aqueous solution of calcium dihydrogenphosphate (YONEYAMA CHEMICAL INDUSTRIES Co., Ltd.) was used in place of magnesium dihydrogenphosphate solution.
Comparative Example 1 A piece of the steel sheet was surface-conditioned (Pl-Zn manufactured by NIHON PARKERIZING Co., Ltd.) and was then treated with zinc phosphate (PB-3322 manufactured by NIHON PARKERIZING Co., Ltd.) to prepare a zinc phosphate-treated galvanized steel sheet with a coating amount of 0.7g/m 2 Comparative Example 2 Using a roll coater, the aqueous solution of magnesium dihydrogenphosphate was applied onto the zinc phosphatetreated galvanized steel sheet of Comparative Example 1, and the sheet was dried while the temperature of the sheet was maintained at 100 0 C. The weight of the applied coating as determined by the difference between the weight of the sheet before coating and the weight of the sheet after coating was adjusted to 0.7g/m 2 Comparative Example 3 Using a roll coater, an emulsion of modified nonionic polyethylene wax (Chemicerac SH5200 manufactured by SANYO CHEMICAL INDUSTRIES Co., Ltd.) was applied onto the zinc phosphate-treated galvanized steel sheet of Comparative Example 1, and the sheet was dried while the temperature of the sheet was maintained at 100 0 C. The weight of the applied coating as determined by the difference between the weight of the sheet before coating and the weight of the sheet after coating was adjusted to O.lg/m 2 Procedure for Performance Evaluation Presence/absence of wax: The sample sheets of Examples 1 through 6 and Comparative Examples 1 through 3 were each degreased by sonication in a solvent (n-hexane) for 5 minutes and were subjected to analysis by FT-IR. The presence of wax was determined by whether peaks appeared at 2800 to 3000cm 1 Workability for forming a U-bead: Rust proof oil (noxrust 550HN manufactured by PARKER INDUSTRIES Co., Ltd.) was applied to each sample sheet in an amount of about 1.5g/m 2 (per one side). The sample sheets were then left overnight and were each cut into 30mm x 300mm strips, which were then immersed in a wash oil (Daphne oil coat manufactured by IDEMITSU KOSAN Co., Ltd.) and were subsequently wiped by sponge roll. The rolled 11 strips were sequentially beaded under the following conditions: BHF 1 ton; height of bead 40mm; beading punch R 5mm; beading die R imm; punch R 5mm; and work speed Ratings were given as follows: a cross indicates that formation of a single bead caused cracking; a triangle indicates that formation of 2 to 10 beads caused cracking; a circle indicates that 10 or more beads could be formed, but
S
only with some scuffs; and a double circle indicates that or more beads could be formed without causing any cracks or scuffs.
Coat adhesion: Each sample sheet was degreased in a commercial alkaline degreasing solution (pH 10.5, 40 0
C,
immersed for 1 minute) and was subjected to electrodeposition coating (V20 manufactured by NIPPON PAINT Co., Ltd., 20p, 1700, baked for 20 minutes). After being left for one day and night, the samples were immersed in warm water at 50 0 C. After 10 days, the samples were taken out of the water bath and cuts were made in a Imm grid pattern. Using a strip of adhesive tape, how easy the coating can be peeled was determined. Ratings were given as follows: a double circle indicates that the coating peeled in 0% of the area; a circle indicates that the coating peeled in less than 5% of the area; a triangle indicates that the coating peeled in 5 to 50% of the area; and a cross indicates that the coating peeled in more than 50% of the area.
12 The results are shown in Table 1 below. As can be seen, each of the sample sheets of Examples of the present invention exhibited better workability than did the sample sheets of Comparative Examples. The workability, as well as the coat adhesion, was significantly low for the sample sheets of Comparative Examples.
Table 1 No Presence Workability Coat /Absence adhesion of wax Ex. 1 Present 2 3 4 is 6 Comp. Ex. 1 Absent A 2 X 3 L x INDUSTRIAL APPLICABILITY The present invention provides a phosphate-treated galvanized steel sheet that has better workability than ever before. Not only are the steel sheets of the present invention free of hazardous substances such as chromium but they also are easy to make, are less expensive, and thus are suited for various applications, including automobiles, home electric 13 appliances, and building materials.
Claims (3)
1. A phosphate-treated galvanized steel sheet with improved workability having a phosphate layer deposited on the surface thereof, characterized in that the phosphate layer contains a polyolefin wax or a modified polyolefin wax.
2. A method for producing the phosphate-treated galvanized steel sheet of claim 1, characterized in that, subsequent to the application of phosphate onto the surface of the galvanized steel sheet, an aqueous solution containing a polyolefin wax or a modified polyolefin wax along with phosphate ions and polyvalent metal ions is applied over the phosphate layer and is then dried.
3. The method according to claim 2 for producing the phosphate-treated galvanized steel sheet, characterized in that the polyvalent metal ion is one or two or more selected from the group consisting of Mg 2 Mn2+, Ca 2 Zn2+ Ni2+ Co 2 and A13+.
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
PCT/JP2000/007774 WO2002036854A1 (en) | 2000-11-06 | 2000-11-06 | Zinc-based metal plated steel sheet treated with phosphate excellent in formability and method for producing the same |
Publications (2)
Publication Number | Publication Date |
---|---|
AU2001210565A1 AU2001210565A1 (en) | 2002-07-18 |
AU2001210565B2 true AU2001210565B2 (en) | 2005-04-21 |
Family
ID=11736654
Family Applications (2)
Application Number | Title | Priority Date | Filing Date |
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AU1056501A Pending AU1056501A (en) | 2000-11-06 | 2000-11-06 | Zinc-based metal plated steel sheet treated with phosphate excellent in formability and method for producing the same |
AU2001210565A Ceased AU2001210565B2 (en) | 2000-11-06 | 2000-11-06 | Zinc-based metal plated steel sheet treated with phosphate excellent in formability and method for producing the same |
Family Applications Before (1)
Application Number | Title | Priority Date | Filing Date |
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AU1056501A Pending AU1056501A (en) | 2000-11-06 | 2000-11-06 | Zinc-based metal plated steel sheet treated with phosphate excellent in formability and method for producing the same |
Country Status (5)
Country | Link |
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EP (1) | EP1338676A1 (en) |
KR (1) | KR20030045127A (en) |
AU (2) | AU1056501A (en) |
CA (1) | CA2427492A1 (en) |
WO (1) | WO2002036854A1 (en) |
Family Cites Families (3)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JP2850183B2 (en) * | 1993-04-15 | 1999-01-27 | 新日本製鐵株式会社 | Manufacturing method of non-delamination type lubricated plated steel sheet which can omit press oil |
EP0653502A3 (en) * | 1993-11-11 | 1995-08-09 | Nihon Parkerizing | Composite article of steel plated with a metal containing zinc and production process. |
JPH08252520A (en) * | 1995-03-20 | 1996-10-01 | Nippon Steel Corp | Surface-treated steel sheet having excellent press working characteristics and method for producing the same |
-
2000
- 2000-11-06 AU AU1056501A patent/AU1056501A/en active Pending
- 2000-11-06 AU AU2001210565A patent/AU2001210565B2/en not_active Ceased
- 2000-11-06 EP EP00971790A patent/EP1338676A1/en not_active Withdrawn
- 2000-11-06 WO PCT/JP2000/007774 patent/WO2002036854A1/en not_active Application Discontinuation
- 2000-11-06 KR KR10-2003-7005547A patent/KR20030045127A/en not_active Ceased
- 2000-11-06 CA CA002427492A patent/CA2427492A1/en not_active Abandoned
Also Published As
Publication number | Publication date |
---|---|
EP1338676A1 (en) | 2003-08-27 |
KR20030045127A (en) | 2003-06-09 |
WO2002036854A1 (en) | 2002-05-10 |
CA2427492A1 (en) | 2003-04-30 |
AU1056501A (en) | 2002-05-15 |
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