WO2017026683A1 - Zinc flash plating solution for galvanized steel sheet having excellent surface appearance, method for manufacturing galvanized steel sheet using same, and galvanized steel sheet - Google Patents

Zinc flash plating solution for galvanized steel sheet having excellent surface appearance, method for manufacturing galvanized steel sheet using same, and galvanized steel sheet Download PDF

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WO2017026683A1
WO2017026683A1 PCT/KR2016/007790 KR2016007790W WO2017026683A1 WO 2017026683 A1 WO2017026683 A1 WO 2017026683A1 KR 2016007790 W KR2016007790 W KR 2016007790W WO 2017026683 A1 WO2017026683 A1 WO 2017026683A1
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steel sheet
zinc
electro
plating
plating solution
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PCT/KR2016/007790
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French (fr)
Korean (ko)
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WO2017026683A8 (en
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정진호
최양호
임상배
이원휘
최효진
한현섭
최용환
정종운
송영식
염준성
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주식회사 포스코
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Priority to CN201680047478.7A priority Critical patent/CN107923056B/en
Priority to JP2018506512A priority patent/JP6588621B2/en
Publication of WO2017026683A1 publication Critical patent/WO2017026683A1/en
Publication of WO2017026683A8 publication Critical patent/WO2017026683A8/en

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    • CCHEMISTRY; METALLURGY
    • C25ELECTROLYTIC OR ELECTROPHORETIC PROCESSES; APPARATUS THEREFOR
    • C25DPROCESSES FOR THE ELECTROLYTIC OR ELECTROPHORETIC PRODUCTION OF COATINGS; ELECTROFORMING; APPARATUS THEREFOR
    • C25D5/00Electroplating characterised by the process; Pretreatment or after-treatment of workpieces
    • C25D5/10Electroplating with more than one layer of the same or of different metals
    • CCHEMISTRY; METALLURGY
    • C21METALLURGY OF IRON
    • C21DMODIFYING THE PHYSICAL STRUCTURE OF FERROUS METALS; GENERAL DEVICES FOR HEAT TREATMENT OF FERROUS OR NON-FERROUS METALS OR ALLOYS; MAKING METAL MALLEABLE, e.g. BY DECARBURISATION OR TEMPERING
    • C21D8/00Modifying the physical properties by deformation combined with, or followed by, heat treatment
    • C21D8/02Modifying the physical properties by deformation combined with, or followed by, heat treatment during manufacturing of plates or strips
    • 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
    • C23GCLEANING OR DE-GREASING OF METALLIC MATERIAL BY CHEMICAL METHODS OTHER THAN ELECTROLYSIS
    • C23G1/00Cleaning or pickling metallic material with solutions or molten salts
    • C23G1/02Cleaning or pickling metallic material with solutions or molten salts with acid solutions
    • CCHEMISTRY; METALLURGY
    • C25ELECTROLYTIC OR ELECTROPHORETIC PROCESSES; APPARATUS THEREFOR
    • C25DPROCESSES FOR THE ELECTROLYTIC OR ELECTROPHORETIC PRODUCTION OF COATINGS; ELECTROFORMING; APPARATUS THEREFOR
    • C25D21/00Processes for servicing or operating cells for electrolytic coating
    • C25D21/12Process control or regulation
    • CCHEMISTRY; METALLURGY
    • C25ELECTROLYTIC OR ELECTROPHORETIC PROCESSES; APPARATUS THEREFOR
    • C25DPROCESSES FOR THE ELECTROLYTIC OR ELECTROPHORETIC PRODUCTION OF COATINGS; ELECTROFORMING; APPARATUS THEREFOR
    • C25D3/00Electroplating: Baths therefor
    • CCHEMISTRY; METALLURGY
    • C25ELECTROLYTIC OR ELECTROPHORETIC PROCESSES; APPARATUS THEREFOR
    • C25DPROCESSES FOR THE ELECTROLYTIC OR ELECTROPHORETIC PRODUCTION OF COATINGS; ELECTROFORMING; APPARATUS THEREFOR
    • C25D3/00Electroplating: Baths therefor
    • C25D3/02Electroplating: Baths therefor from solutions
    • C25D3/22Electroplating: Baths therefor from solutions of zinc
    • CCHEMISTRY; METALLURGY
    • C25ELECTROLYTIC OR ELECTROPHORETIC PROCESSES; APPARATUS THEREFOR
    • C25DPROCESSES FOR THE ELECTROLYTIC OR ELECTROPHORETIC PRODUCTION OF COATINGS; ELECTROFORMING; APPARATUS THEREFOR
    • C25D5/00Electroplating characterised by the process; Pretreatment or after-treatment of workpieces
    • C25D5/34Pretreatment of metallic surfaces to be electroplated
    • C25D5/36Pretreatment of metallic surfaces to be electroplated of iron or steel
    • CCHEMISTRY; METALLURGY
    • C25ELECTROLYTIC OR ELECTROPHORETIC PROCESSES; APPARATUS THEREFOR
    • C25DPROCESSES FOR THE ELECTROLYTIC OR ELECTROPHORETIC PRODUCTION OF COATINGS; ELECTROFORMING; APPARATUS THEREFOR
    • C25D5/00Electroplating characterised by the process; Pretreatment or after-treatment of workpieces
    • C25D5/627Electroplating characterised by the visual appearance of the layers, e.g. colour, brightness or mat appearance
    • CCHEMISTRY; METALLURGY
    • C25ELECTROLYTIC OR ELECTROPHORETIC PROCESSES; APPARATUS THEREFOR
    • C25DPROCESSES FOR THE ELECTROLYTIC OR ELECTROPHORETIC PRODUCTION OF COATINGS; ELECTROFORMING; APPARATUS THEREFOR
    • C25D7/00Electroplating characterised by the article coated

Definitions

  • the present invention relates to a zinc flash plating solution which can provide an electrogalvanized steel sheet having an excellent surface appearance, and a method of manufacturing an electrogalvanized steel sheet using the same and an electrogalvanized steel sheet prepared therefrom.
  • Electro-galvanized steel sheet has a beautiful appearance, excellent paintability, and easy to control the amount of galvanized coating, so it is widely applied to high-end home appliances and automobile exterior plates.
  • domestic electro-galvanized steel sheet is mainly used chromium-free or anti-fingerprint products of about 1 ⁇ m.
  • Patent Literature 1 discloses a method of pickling a steel sheet with an acidic aqueous solution containing 50 to 3,000 ppm of nitrogen organic compound, which is adsorbed on the surface of the steel sheet to uniformize the plating stain.
  • Patent Document 2 discloses a method of improving whiteness and gloss by pickling with an aqueous sulfuric acid solution containing colloidal silica having an average particle diameter of 4 to 200 nm to reduce irregularities on the surface of the steel sheet.
  • the cold rolled steel pole surface state cannot be made exactly the same according to the components contained in the cold rolled steel or the heat treatment history. After the difference occurs in the structure and orientation of the plating layer, as a result of the color difference of the electrogalvanized steel sheet.
  • a composition variation due to the structure of the cold rolled steel sheet or the concentration of components occurs, it is difficult to homogenize the cold rolled steel sheet surface by pickling, so there is a problem of spots locally on the galvanized layer.
  • Patent Document 3 proposes a hydrochloric acid-based electrogalvanized solution containing polyethylene glycol, vanillin, and Mg
  • Patent Document 4 proposes Cu, In, Sn, Pb, to suppress epitaxial growth of zinc in the electroplating solution.
  • the present invention proposes a method for miniaturizing the plating structure and removing stains by adding and vacancy by adding elements such as Ge, Sb, Cd, and Ag.
  • Patent Literatures 5, 6, and 7 are electro-galvanized when electro-galvanizing is performed after plating metals such as Ni, Co, Fe, Ti, Mn, Cu, Cr, Mo, and W up to several hundred mg / m 2 or less. It is disclosed that the stain of the steel sheet can be removed and homogenized.
  • Ni flash treatment is the best in terms of plating adhesion, economical efficiency, manageability, and effect, but due to human health of Ni, it is not suitable as a base treatment for electroplating, and wastewater treatment problems are seriously taken.
  • Co is a very expensive metal, it is not economical, Fe is oxidized during the electroplating process sludge is generated, it is very difficult to manage the solution.
  • Cu is substituted plating with Fe of the cold rolled steel sheet even if electricity is not applied, it is very difficult to manage the adhesion amount, and the zinc and the standard reduction potential difference are very large, thereby deteriorating the corrosion resistance of the galvanized steel sheet. Even in the case of other metals, it is not economical by flash treatment for electro zinc plating in terms of human health and plating efficiency.
  • Patent Documents 8 and 9 a method of improving the surface appearance of an electrogalvanized steel sheet by flash treatment with a Zn-based alloy electroplating solution has been proposed.
  • this method has the effect of improving the whiteness and surface appearance to a certain level than without the flash treatment, the unevenness and staining of the epitaxial growth of the galvanized layer caused by the component thickening of the surface of the cold rolled steel sheet and the nonuniformity of the oxidation level.
  • it is difficult to manage the constant concentration of the alloy component ions in the solution it is difficult to manage the solution in the continuous electroplating process.
  • Patent Document 1 JP1997-059788
  • Patent Document 2 Japanese Laid-Open Patent Publication JP2003-306790
  • Patent Document 3 Korean Patent Publication No. KR2003-0049811
  • Patent Document 4 Japanese Laid-Open Patent Publication JP2001-040494
  • Patent Document 5 Japanese Laid-Open Patent Publication JP1996-165593
  • Patent Document 6 Japanese Laid-Open Patent Publication JP1996-049091
  • Patent Document 7 JP1997-202993
  • Patent Document 8 Korean Patent Application No. KR2012-0151505
  • Patent Document 9 Korean Application Patent KR2012-0112818
  • One aspect of the present invention is the non-uniformity of the plating structure, color, plating thickness, etc. of the electro-zinc plated steel sheet generated due to the local component difference, the oxidation degree difference of the surface of the cold-rolled steel sheet used as the base steel sheet of the galvanized steel sheet It is to provide a zinc flash plating solution for an electrogalvanized steel sheet capable of removing the electroplated steel sheet, a method for producing an electrogalvanized steel sheet using the same and an electrogalvanized steel sheet prepared therefrom.
  • One aspect of the present invention provides a zinc flash plating solution for an electrogalvanized steel sheet having an excellent surface appearance including zinc (Zn) ions, amine organic compounds and other unavoidable impurities.
  • Another aspect of the invention the step of degreasing and pickling the steel sheet; Performing zinc flash plating on the base steel sheet using a zinc flash plating solution; And electro-galvanizing the zinc flash-plated base steel sheet, wherein the zinc flash plating solution uses the above-described plating solution.
  • the zinc flash plating solution uses the above-described plating solution.
  • the electro-galvanized steel sheet produced by the present invention when used in automobiles, home appliances, etc., has the effect of reducing the irregularities and stains generated after coating.
  • the zinc flash plating solution according to the present invention has a high plating efficiency and is suitable for application to a continuous electroplating process for mass production.
  • Figure 1 shows the results of observing the surface of the invention example 1-1 in the embodiment of the present invention.
  • Figure 2 shows the results of observing the surface of Comparative Example 1-1 in the embodiment of the present invention (where 1 represents a stain generated on the surface).
  • the present inventors have identified the cause of unevenness of plating and plating structure on the surface of the galvanized steel when degreasing and pickling in a conventional manner without flash treatment before plating, and the method for solving the problem Studied.
  • Cold rolled steel sheet which is used as a base steel sheet of electro-zinc plating, is manufactured through a number of heat treatment, pickling, and rolling processes. In this manufacturing process, trace alloy components contained in the steel are locally concentrated on the surface of the steel sheet, or the oxide layer thickness of the steel sheet surface. There is a slight deviation in.
  • Electro zinc plating process is carried out on the base steel sheet such as cold rolled steel sheet is a process in which the zinc ions contained in the plating solution is reduced and precipitated on the surface of the base steel sheet when electricity is applied using the base steel sheet as a cathode. It is the process of rearranging crystalline metal on the surface of steel sheet.
  • the direction of the galvanized particles is determined by the arrangement of iron atoms in the pole surface layer of the steel sheet and the components and the oxidation level of the surface.
  • the inventors of the present invention when the zinc flash plating prior to the electro-galvanizing of the base steel sheet, even if the electro-galvanization of ordinary galvanized steel sheet having a uniform appearance It was confirmed that it can be provided.
  • the inventors of the present invention optimize the components of the plating solution used in the zinc flash plating, and by performing zinc flash plating using them, the localization of the galvanized structure caused by the concentration of components on the surface of the cold-rolled steel sheet, non-uniformity of the oxide layer By resolving the phosphorous nonuniformity and the thickness of the galvanized layer, it was confirmed that an electrogalvanized steel sheet having excellent surface appearance was obtained, and thus the present invention was completed.
  • Zinc flash plating solution for an electrogalvanized steel sheet preferably comprises zinc (Zn) ions, amine-based organic compounds and other unavoidable impurities.
  • the zinc (Zn) ions are sulfuric acid (SO 4 ) -based or hydrochloric acid (HCl) -based, preferably contained at a concentration of 1 ⁇ 150g / L.
  • the concentration of zinc (Zn) ions is less than 1 g / L, the plating efficiency is lowered, and the limit current density, which is the maximum current density that can be plated, is lowered, thereby making it difficult to operate high-speed electroplating.
  • the concentration exceeds 150g / L, the zinc content in the plating solution is high, the raw material price is increased, there is a problem that Zn waste due to the solution loss is increased.
  • the present inventors have tried to add various types of organic and inorganic compounds to the plating solution containing zinc (Zn) ions, but the added compound bonds too strongly to the surface of the steel sheet and the surface of the plating layer, or the content is appropriate. Exceeding the above resulted in the precipitation of zinc in the subsequent electro zinc plating is suppressed, the burning phenomenon occurs, the plating quality was deteriorated. On the other hand, if the bonding strength is too weak, or the content is insufficient, the appearance is good after electro zinc plating. It was confirmed that it could not be obtained.
  • the lone pair of electrons included in the nitrogen atom forms a bond with the metal
  • the electron density of the nitrogen varies depending on the number of hydrocarbons, the chain length, and the end group bonded to the nitrogen atom.
  • the amine group has a stronger adsorption force with the metal surface because the OH group acts to push electrons toward the nitrogen atom.
  • the electron density of nitrogen may increase, but the adsorption force may be weakened because carbon hydrogen interferes with the bonding of nitrogen and the metal surface.
  • the zinc flash plating solution contains an amine-based organic compound having the property of easily adsorbing on the surface of the base steel sheet and the zinc plated layer, in addition to the zinc (Zn) ions. You can get it.
  • the difference in oxidation degree localized on the surface of the cold rolled steel and the nonuniform concentration of the components contained in the steel cause a difference between the rate of precipitation of zinc (Zn) ions and the rate of epitaxy growth in the early stage of electrogalvanization.
  • Zn zinc
  • epitaxy growth in the early stage of electrogalvanization.
  • the amine-based compound is adsorbed on the surface of the steel sheet irrespective of the state of the cold-rolled steel sheet surface it is possible to uniformly control the nucleation rate of the initial electroplating.
  • the nuclei of zinc plating are formed only at the beginning of the plating, and during the plating, zinc tends to grow only without nucleation. That is, in order to generate secondary nucleation in the electro-zinc plating process, a sufficient overvoltage than a normal level is applied, or zinc plating is sufficiently progressed so that the growth rate of zinc is slowed down compared to the applied overvoltage. Therefore, the structure and orientation of the electro-galvanized layer formed under ordinary electro-zinc plating conditions have a certain relationship with the orientation of the cold-rolled steel sheet, and are directly affected by the orientation of the cold-rolled steel sheet during ultra-thin galvanizing at the level of flash plating. .
  • the zinc flash plating solution for electrogalvanized steel sheet of the present invention has a technical significance in that it contains an amine organic compound in addition to zinc (Zn) ions.
  • a primary to tertiary amine organic compound as the amine organic compound, more preferably an aliphatic containing at least one nitrogen atom in the compound molecule and having a chain length of 1 to 5 carbon atoms. It is preferable that the hydrocarbon per 1 nitrogen atom of an aliphatics structure is 1 type, or 2 or more types of mixtures chosen from the compound which has 1-3 bonds.
  • an amine In order for an amine to maintain a bond with the surface of a metal (steel plate), it is preferable to have a lone pair of electrons at a nitrogen atom.
  • a metal steel plate
  • the quaternary amine compound bonded with a hydrocarbon having an aliphatic structure has a problem in that the solubility in the aqueous solution decreases as the molecular weight increases, so that dissolution is impossible or precipitation occurs.
  • the primary amine-based organic compound containing one nitrogen atom in the compound molecule has a high boiling point and is soluble in aqueous solution, such as ethanolamine or amino propanol. It can be selected from alcohols.
  • a secondary amine organic compound containing one nitrogen atom in the molecule it can be selected from diethanolamine, methylethanolamine, etc., and tertiary amine system containing one nitrogen atom in the molecule.
  • the organic compound may be selected from triethylamine, diethylaminoethanol, diethanolethylamine, triethanolamine, and the like.
  • linear structures such as ethylenediamine, diethylenetriamine, triethylenetetramine, diaminopropane, spermidine, and spermine
  • Cyclic or steric structures such as polyamine, cyclen (1,4,7,10-tetraazacyclododecane), cyclam (1,4,8,11-tetraazacyclotetradecane), hexamethylenetetramine (hexamethylentetramine) It can be selected from a water-soluble polyamine and a water-soluble amine polymer.
  • three-dimensional water-soluble polyamines and water-soluble amine-based polymers have a large number of nitrogen atoms, and the non-covalent electron pairs of nitrogen atoms are exposed to the outside of the molecule, and thus have a high possibility of bonding with metal, thereby facilitating adsorption. There is a more beneficial effect on improving the surface of the steel sheet.
  • the amine organic compound of the present invention is not limited to the amine compound described above, and may be used alone or in combination of two or more amine organic compounds.
  • Such an amine organic compound is preferably contained in the plating solution at 0.05 ⁇ 10g / L.
  • the concentration of the amine organic compound is less than 0.05 g per 1 L of the plating solution, the amount of the organic compound adsorbed on the metal surface is small, and the adsorption reaction of the organic compound during the plating process is less than that of the zinc precipitation reaction, thereby improving the appearance after galvanizing. Is not big.
  • the content exceeds 10g, the adsorption of the organic compound is excessive and the zinc precipitation reaction is suppressed, thereby causing a burning phenomenon.
  • the zinc flash plating solution for electro-galvanized steel sheet of the present invention containing zinc (Zn) ions and an amine organic compound preferably has a pH of 1.0 to 5.0.
  • the pH of the zinc flash plating solution is less than 1.0, the rate of reduction of hydrogen in the solution increases during electro-galvanizing of the base steel sheet as a cathode, thereby decreasing the amount of deposition of zinc plating. A problem that does not precipitate occurs.
  • the pH exceeds 5.0 there is a problem that precipitation occurs while inevitable impurities such as iron form hydroxides from zinc ions or steel sheets.
  • the zinc flash plating solution of the present invention may further include a supporting salt such as sodium sulfate, potassium sulfate, ammonium sulfate, potassium chloride or sodium chloride for the purpose of improving conductivity.
  • a supporting salt such as sodium sulfate, potassium sulfate, ammonium sulfate, potassium chloride or sodium chloride for the purpose of improving conductivity.
  • the supporting salt is preferably contained in less than 200g / L, even if the supporting salt in the above range, the electro-galvanized steel sheet produced by electro-galvanizing after zinc flash plating may have a uniform plating appearance.
  • a complexing agent may be further included to suppress precipitation of iron, nickel, manganese and other impurity ions eluted from the steel sheet and inevitably contained in the zinc flash plating solution.
  • the complexing agent for example, citric acid, sodium citrate, sodium heptonate and the like can be used, and the content thereof is preferably 30 g / L or less. Even if the complexing agent is included in the above range, the galvanized steel sheet prepared by zinc plating after electroplating may have a uniform plating appearance.
  • the supporting salts and the complexing agents may be selectively added to the zinc flash plating solution of the present invention, and even if these components are not added, they do not significantly affect the appearance of the galvanized steel sheet produced.
  • the steel sheet that can be used as the base steel sheet is not particularly limited, any steel sheet for the electro-galvanized steel sheet is possible, but preferably may be a cold-rolled steel sheet.
  • the plating solution of the present invention when the zinc flash plating, and the plating amount in the state in which the temperature of the plating solution is adjusted to room temperature (approximately 25 ° C.) to 80 ° C. and the current density is applied at 1 to 100 A / dm 2 . It is preferable to carry out so that it may become 10-2000 mg / m ⁇ 2> .
  • the temperature of the zinc flash plating solution exceeds 80 °C, the amount of solution evaporation is excessive, the management of the plating solution is difficult, there is a risk of causing corrosion in the working environment.
  • the plating effect is excellent even if the temperature of the zinc flash plating solution is kept at room temperature, it is more preferable to maintain at 40 to 65 ° C because the plating efficiency is good and the management is good.
  • the plating efficiency is low, and in order to obtain an appropriate level of zinc flash plating amount, there is a problem that the plating takes a long time, which is not suitable in the continuous plating process.
  • it exceeds 100A / dm 2 there is a problem that burning occurs in the zinc flash plating process, causing stains, or poor adhesion of the plating layer formed after the subsequent electro-galvanization.
  • the zinc adhesion amount satisfies the range of 10 to 2000 mg / m 2 , and when the zinc adhesion amount is less than 10 mg / m 2, the appearance improvement effect of the galvanized steel sheet is insignificant.
  • the flash plating layer may be locally eluted to cause staining.
  • the base steel sheet after zinc flash plating is completed includes a flash plating layer, and by performing electro zinc plating on the base steel sheet, a general electro galvanized steel sheet having a zinc adhesion amount of 5 to 100 g / m 2 can be produced. Can be.
  • the conditions of the electro-zinc plating are not particularly limited, and may be carried out in conditions which are usually performed, such as sulfuric acid or hydrochloric acid-based electro zinc plating baths.
  • the electro-galvanized steel sheet of the present invention obtained by completing the above electro-zinc plating comprises an electro-galvanized layer on the base steel sheet, and has excellent surface appearance.
  • a zinc flash plating solution was prepared by mixing and dissolving an amine-based organic compound ethanolamine and hexamethyltetramine. At this time, the amine-based organic compound was added so that the total amount is 2.5 ⁇ 3.5g / L by weight per 1L solution. Thereafter, sulfuric acid was added to adjust the pH of the zinc flash plating solution to 1.5 to 2.5, and then heated to 45 to 55 ° C.
  • Zinc flash plating was performed by immersing the prepared cold-rolled steel sheet in a heated zinc flash plating solution for 1 second.
  • the current density was controlled so that the coating weight was 50 to 2000 mg / m 2 , and the current was 1.5 to 75 A / dm 2 . Density was applied.
  • the zinc-plated cold-rolled steel sheet is subjected to electro-galvanization in a sulfuric acid-based galvanized solution having a zinc (Zn) ion concentration of 50-150 g / L, the zinc plating amount is 20-40 g / m 2 . Water was washed with pure water to obtain an electrogalvanized steel sheet.
  • Zinc (Zn) ion concentration was dissolved using zinc sulfate to 20 ⁇ 30g / L, and then sulfuric acid was added to adjust the pH of the solution to 1.5 ⁇ 2.5 to prepare a zinc flash plating solution. Then, the zinc flash plating solution was heated to 45 ⁇ 55 °C.
  • the zinc (Zn) ion was dissolved in a concentration of 20 to 30 g / L, and then one of the nitrogen-containing compound thiourea and the quaternary amine organic compound cetyltrimethylammonium bromide and choline was selected. Mixing and dissolving prepared a zinc flash plating solution. Thereafter, sulfuric acid was added to adjust the pH of the zinc flash plating solution to 1.5 to 2.5, and then heated to 45 to 55 ° C.
  • a zinc flash plating solution was prepared by mixing and dissolving an amine-based organic compound ethanolamine and hexamethyltetramine. At this time, the amine-based organic compound was added so that the total amount is 25 ⁇ 35g / L by weight per 1L solution. Thereafter, sulfuric acid was added to adjust the pH of the zinc flash plating solution to 1.5 to 2.5, and then heated to 45 to 55 ° C.
  • the cold rolled steel surface may be provided with a relatively very uniform material depending on the manufacturing method.
  • the electro-galvanized steel sheet is directly applied to the cold rolled steel sheet subjected to normal degreasing and pickling only without performing zinc flash plating on the cold rolled steel sheet.
  • the occurrence of stains was checked first, and the same cold rolled steel was taken and used as a holding steel sheet.
  • the stain generation level was set based on the following criteria.
  • The stain is clearly seen by the naked eye, and the difference in plating structure is apparent when the microscope is observed.
  • the color difference of the electrogalvanized steel sheet may be generated depending on the trace alloy component, manufacturing conditions, and coils of the base steel sheet.
  • the galvanized steel sheet is used for painting, so the color difference of each coil does not affect the quality characteristics, but for home appliance steel plate, the color needs to be kept constant. .
  • the color difference is calculated based on the average color of 12 points manufactured and measured under the same conditions in order to quantitatively compare the level of staining. Calculated as color deviation with square root.
  • the average whiteness was 2 to 3 levels lower than the zinc flash treatment, and the color deviation was measured to be 2.5 to 4.0 in the galvanized steel sheets plated from different cold rolled steel sheets. This shows that the minute difference of the surface of the cold rolled steel sheet has a great influence on the color of the surface after electroplating. In general, when the color difference is 2.0 or more, it is known that the difference between the two colors can be easily determined by the naked eye. Since the color deviation is at least 2.5 or more, the color difference becomes easily recognizable, making it difficult to produce a uniform product.
  • the color variation according to the type of cold rolled steel tended to increase more, which is due to the difference in concentration and pH by plating with a flash plating solution having a relatively low zinc concentration and a high pH compared to a conventional electrogalvanizing solution. It seems to have influenced the frequency of nucleation at the initial stage of plating, but the difference or nonuniformity of the surface of cold rolled steel sheet could be considered to be more weighted and transferred during the galvanizing process.
  • the amide compound does not have a significant effect on improving the appearance of the electroplated steel sheet, and in the case of a compound containing sulfur such as thiourea, it is believed that the amide compound has an improvement in product appearance due to the surface adsorption effect by sulfur. .
  • sulfur-containing molecules such as thiourea are easily electrolyzed at the anode, a white precipitate occurs as the plating proceeds, which is not suitable for the continuous electrogalvanization process.
  • Cetyltrimethylammonium bromide is a kind of surfactant and is a quaternary amine compound like choline. For Comparative Examples 3-5 to 3-8 using these compounds as additives, similar effects to thiourea were seen. These results indicate that choline molecules are not surfactants classified as hydrophobic groups and hydrophilic groups, and thus the molecules are weakly adsorbed on the steel sheet or zinc metal surface, whereas cetyltrimethylammonium is a surfactant that distinguishes hydrophobic and hydrophilic regions, so It is because the tendency to arrange
  • the quaternary amine polymer compound was to be added below 1 g / L, but electro zinc coating was not possible because precipitation occurred in the acidic zinc plating solution.
  • Zinc flash plating was carried out using the same additive as inventive example 1, but in Comparative Examples 4-1 to 4-4 in which the content was too high, the zinc plating layer turned black in the edge region of the specimen where the current was concentrated. Burning phenomenon could be confirmed.
  • the burning phenomenon refers to a phenomenon in which hydroxide is mixed in the plating layer and blackening occurs because smooth plating is not performed when the plating speed exceeds a critical plating speed.
  • the additive that is, the amine organic compound as little as possible while maintaining an appropriate level.
  • the adhesion between the base steel sheet and the plating layer is very excellent.
  • the flash treatment is performed with a zinc flash solution containing an additive before electro-galvanizing, adhesion between the plating layer and the base steel sheet may be degraded. Therefore, in order to evaluate the adhesion between the plated layer and the base steel sheet, the steel sheet was bent to 90 ° using a mold having a radius of curvature of 0.5 mm, and then the inside of the bent portion was peeled off with a tape to evaluate the adhesion between the base steel and the zinc plated layer.
  • Example 1 and 2 show the surfaces of the electrogalvanized steel sheets of Inventive Example 1-1 and Comparative Example 1-1, respectively.

Abstract

The present invention relates to a zinc flash plating solution which can provide a galvanized steel sheet having an excellent surface appearance, a method for manufacturing a galvanized steel sheet using the same, and a galvanized steel sheet manufactured thereby.

Description

표면외관이 우수한 전기아연도금강판용 아연 플래쉬 도금 용액, 이를 이용한 전기아연도금강판의 제조방법 및 전기아연도금강판Zinc Flash Plating Solution for Electro Zinc Plated Steel Sheet with Excellent Surface Appearance, Manufacturing Method of Electro Zinc Plated Steel Sheet Using the Same and Electro Zinc Plated Steel Sheet
본 발명은 표면외관이 우수한 전기아연도금강판을 제공할 수 있는 아연 플래쉬 도금 용액, 이를 이용한 전기아연도금강판의 제조방법과 이로부터 제조된 전기아연도금강판에 관한 것이다.The present invention relates to a zinc flash plating solution which can provide an electrogalvanized steel sheet having an excellent surface appearance, and a method of manufacturing an electrogalvanized steel sheet using the same and an electrogalvanized steel sheet prepared therefrom.
전기아연도금강판은 외관이 미려하고, 도장성이 우수하며 아연도금 부착량 제어가 용이하기 때문에 고급 가전, 자동차 외판 등에 다양하게 적용된다. 특히, 가정용 전기아연도금강판은 1㎛ 내외의 크롬-프리 처리 또는 내지문 처리된 제품이 주로 사용된다. Electro-galvanized steel sheet has a beautiful appearance, excellent paintability, and easy to control the amount of galvanized coating, so it is widely applied to high-end home appliances and automobile exterior plates. In particular, domestic electro-galvanized steel sheet is mainly used chromium-free or anti-fingerprint products of about 1㎛.
이러한 전기아연도금강판의 백색도와 얼룩은 최종 제품의 외관 품질을 직접적으로 결정하게 된다.The whiteness and unevenness of these galvanized steel sheets directly determine the appearance quality of the final product.
최근, 자동차사들은 원가 절감을 위해 도장의 두께를 감소시키거나 도장의 횟수를 줄이는 노력을 기울이고 있다. 그러나, 도장 두께가 감소하면 도금강판의 표면 결함이 도장 표면까지 전사되어 결함으로 나타나는 경향이 있어, 도금강판 표면 품질이 보다 더 엄격하게 관리될 필요가 있다.Recently, automakers have made efforts to reduce the thickness of coatings or reduce the number of coatings in order to reduce costs. However, when the coating thickness decreases, the surface defects of the coated steel sheet tend to be transferred to the painted surface and appear as defects, so that the surface quality of the coated steel sheet needs to be more strictly managed.
이에, 종래에는 전기아연도금강판의 표면 품질, 특히 도금 표면의 얼룩을 저감시키고 백색도를 향상시키기 위해 다양한 방안이 제시되었다.Therefore, in the related art, various methods have been proposed to reduce the surface quality of the galvanized steel sheet, in particular, the unevenness of the plating surface and to improve the whiteness.
예컨대, 특허문헌 1은 질소 유기화합물을 50~3,000ppm 함유하는 산성 수용액으로 강판을 산세하는 방법을 개시하고 있는데, 이는 산성 수용액 내에 함유된 질소 유기화합물이 강판 표면에 흡착되어 균일화 작용을 하여 도금 얼룩을 완화시키고자 한 것이다. 또한, 특허문헌 2에는 평균입경 4~200nm의 콜로이달 실리카를 함유하는 황산 수용액으로 산세 처리하여 강판 표면의 요철을 감소시킴으로써 백색도와 광택을 개선하는 방법이 개시되어 있다.For example, Patent Literature 1 discloses a method of pickling a steel sheet with an acidic aqueous solution containing 50 to 3,000 ppm of nitrogen organic compound, which is adsorbed on the surface of the steel sheet to uniformize the plating stain. To alleviate this. In addition, Patent Document 2 discloses a method of improving whiteness and gloss by pickling with an aqueous sulfuric acid solution containing colloidal silica having an average particle diameter of 4 to 200 nm to reduce irregularities on the surface of the steel sheet.
그러나, 산 용액을 이용하여 도금 전의 냉연강판 표면을 산세하여 개질하더라도, 냉연강판에 함유된 성분이나 열처리 이력에 따라 냉연강판 극표면 상태를 완전히 동일하게 만들 수 없기 때문에, 강종 또는 재질이 달라지면 전기도금 후 도금층의 조직 및 배향에 차이가 발생하고, 결과적으로 전기아연도금강판의 색상 차이가 발생한다. 뿐만 아니라, 냉연강판 표면의 조직이나 성분 농화에 의한 조성 편차가 발생하는 경우, 산세에 의해 냉연강판 표면을 균질화하는 것은 한계가 있으므로, 전기아연도금층에 국부적으로 얼룩이 발생하는 문제가 있다.However, even if the surface of the cold rolled steel sheet before acid plating is pickled and modified by using an acid solution, the cold rolled steel pole surface state cannot be made exactly the same according to the components contained in the cold rolled steel or the heat treatment history. After the difference occurs in the structure and orientation of the plating layer, as a result of the color difference of the electrogalvanized steel sheet. In addition, in the case where a composition variation due to the structure of the cold rolled steel sheet or the concentration of components occurs, it is difficult to homogenize the cold rolled steel sheet surface by pickling, so there is a problem of spots locally on the galvanized layer.
이에, 냉연강판 표면의 국부적인 편차에 의한 얼룩을 제거하고, 냉연강판의 성분이나 표면 상태에 무관하게 일정한 도금 외관을 가질 수 있도록 전기아연도금용액의 성분, 또는 전기도금 조건을 제어하는 방법이 제시되었다.Accordingly, a method of controlling the components of the electro-zinc plating solution or the electroplating conditions to remove stains caused by local deviation of the surface of the cold rolled steel sheet and to have a uniform plating appearance irrespective of the components or surface state of the cold rolled steel sheet is proposed. It became.
예컨대, 특허문헌 3에는 폴리에틸렌글리콜, 바닐린 및 Mg을 함유한 염산계 전기아연도금용액을 제안하고 있으며, 특허문헌 4에서는 전기도금용액에 아연의 에피택시 성장을 억제하고자 Cu, In, Sn, Pb, Ge, Sb, Cd, Ag 등의 원소를 첨가하여 공석시킴으로써 도금조직을 미세화하고 얼룩을 제거하는 방법을 제시하고 있다.For example, Patent Document 3 proposes a hydrochloric acid-based electrogalvanized solution containing polyethylene glycol, vanillin, and Mg, and Patent Document 4 proposes Cu, In, Sn, Pb, to suppress epitaxial growth of zinc in the electroplating solution. The present invention proposes a method for miniaturizing the plating structure and removing stains by adding and vacancy by adding elements such as Ge, Sb, Cd, and Ag.
그러나, 폴리에틸렌글리콜과 같이 전기아연도금용액에 함유된 분자량이 높은 폴리에테르계 유기분자는 불용성 양극을 이용하여 전기도금하는 과정 중에 양극 표면에 유기분자가 전기화학적으로 분해되거나 불용성 양극의 효율을 저하시키고, 용액의 점도가 상승하여 고유속 작업을 저해할 수 있다. 또한 전기아연도금용액에 아연 이외의 금속 이온을 첨가하여 도금층에 공석시키는 경우, 아연과 첨가된 미량 금속의 석출비가 용액 내 농도비와 달라 연속 도금공정 중 용액 내 금속의 성분비가 끊임없이 변화하게 되므로, 균일한 품질의 전기아연도금강판 제조가 어렵고, 도금용액의 조성을 일정하게 관리하기 어렵다. 뿐만 아니라, 아연 이외의 금속이 도금층에 공석되면 가전용 강판에서 백색도를 하락시키거나, 자동차용 아연도금강판의 인산염 처리성을 저해하고 얼룩을 발생시키는 문제점이 있다.However, high molecular weight polyether-based organic molecules, such as polyethylene glycol, are electrochemically decomposed on the surface of the anode during electroplating using an insoluble anode, or the efficiency of the insoluble anode is reduced. As a result, the viscosity of the solution may increase, which may inhibit high flow operation. In addition, when vaccinating the plating layer by adding metal ions other than zinc to the electrogalvanizing solution, the precipitation ratio of zinc and the added trace metal is different from the concentration ratio in the solution, and thus the component ratio of the metal in the solution is continuously changed during the continuous plating process. It is difficult to manufacture a galvanized steel sheet of a high quality, and it is difficult to constantly control the composition of the plating solution. In addition, when metal other than zinc is vacant in the plating layer, there is a problem of decreasing whiteness in the steel sheet for home appliances or inhibiting the phosphate treatment property of automotive galvanized steel sheet and causing staining.
한편, 냉연강판의 재질 차이, 또는 국부적인 성분 농화 등에 의한 전기아연도금층의 불균일성을 억제하는 가장 효과적인 방법으로 전기아연도금 전에 극박의 금속층, 즉 플래쉬 처리하는 방법이 제안되었다. On the other hand, as the most effective method of suppressing the non-uniformity of the electro-galvanized layer due to the difference in the material of the cold-rolled steel sheet or localized component thickening, etc., an ultra-thin metal layer, that is, a method of flash treatment has been proposed.
특허문헌 5, 6 및 7에는 Ni, Co, Fe, Ti, Mn, Cu, Cr, Mo, W 등의 금속을 수백 mg/m2 이하로 도금한 후 전기아연도금을 실시하는 경우, 전기아연도금강판의 얼룩을 제거하고 균질화할 수 있다고 개시하고 있다.Patent Literatures 5, 6, and 7 are electro-galvanized when electro-galvanizing is performed after plating metals such as Ni, Co, Fe, Ti, Mn, Cu, Cr, Mo, and W up to several hundred mg / m 2 or less. It is disclosed that the stain of the steel sheet can be removed and homogenized.
이 중, 도금 밀착성, 경제성, 관리 용이성 및 효과 측면에서는 Ni 플래쉬 처리가 가장 우수하나, Ni의 인체 유해성으로 인해 전기도금용 하지 처리로서 적절하지 않으며, 폐수 처리 문제가 심각하게 받아들여지고 있다. 또한, Co는 매우 고가의 금속으로 경제적이지 못하며, Fe는 전기도금 과정에서 산화되어 슬러지가 발생되어 용액 관리가 매우 어렵다. 뿐만 아니라, Cu는 전기를 인가하지 않더라도 냉연강판의 Fe와 치환도금되므로 부착량 관리가 매우 어렵고 아연과 표준 환원 전위차가 매우 커서 전기아연도금강판의 내식성을 저하시키는 문제가 있다. 기타 다른 금속의 경우에서도 인체 유해성, 도금효율 등의 측면에서 전기아연도금용 플래쉬 처리로 경제적이지 못하다.Among them, Ni flash treatment is the best in terms of plating adhesion, economical efficiency, manageability, and effect, but due to human health of Ni, it is not suitable as a base treatment for electroplating, and wastewater treatment problems are seriously taken. In addition, Co is a very expensive metal, it is not economical, Fe is oxidized during the electroplating process sludge is generated, it is very difficult to manage the solution. In addition, since Cu is substituted plating with Fe of the cold rolled steel sheet even if electricity is not applied, it is very difficult to manage the adhesion amount, and the zinc and the standard reduction potential difference are very large, thereby deteriorating the corrosion resistance of the galvanized steel sheet. Even in the case of other metals, it is not economical by flash treatment for electro zinc plating in terms of human health and plating efficiency.
최근에는, 특허문헌 8 및 9에서와 같이 Zn계 합금전기도금용액으로 플래쉬 처리하여 전기아연도금강판의 표면 외관을 개선하는 방법이 제안되었다. 이러한 방법은 비록 플래쉬 처리를 하지 않은 경우보다 백색도가 개선되고 표면 외관이 일정 수준 개선되는 효과가 있지만, 냉연강판 표면의 성분 농화, 산화 수준의 불균일성으로 인해 발생되는 아연도금층의 에피택시 성장 불균일 및 얼룩을 완전히 제거하지 못하는 단점이 있다. 뿐만 아니라, 용액 내 합금 성분 이온 농도를 일정하게 관리하기가 어렵기 때문에 연속 전기도금공정에서 용액 관리가 어렵다.Recently, as in Patent Documents 8 and 9, a method of improving the surface appearance of an electrogalvanized steel sheet by flash treatment with a Zn-based alloy electroplating solution has been proposed. Although this method has the effect of improving the whiteness and surface appearance to a certain level than without the flash treatment, the unevenness and staining of the epitaxial growth of the galvanized layer caused by the component thickening of the surface of the cold rolled steel sheet and the nonuniformity of the oxidation level. There is a disadvantage that can not be removed completely. In addition, it is difficult to manage the constant concentration of the alloy component ions in the solution, it is difficult to manage the solution in the continuous electroplating process.
(특허문헌 1) 일본공개특허공보 JP1997-059788호(Patent Document 1) JP1997-059788
(특허문헌 2) 일본공개특허공보 JP2003-306790호(Patent Document 2) Japanese Laid-Open Patent Publication JP2003-306790
(특허문헌 3) 한국공개특허 KR2003-0049811호(Patent Document 3) Korean Patent Publication No. KR2003-0049811
(특허문헌 4) 일본공개특허공보 JP2001-040494호(Patent Document 4) Japanese Laid-Open Patent Publication JP2001-040494
(특허문헌 5) 일본공개특허공보 JP1996-165593호(Patent Document 5) Japanese Laid-Open Patent Publication JP1996-165593
(특허문헌 6) 일본공개특허공보 JP1996-049091호(Patent Document 6) Japanese Laid-Open Patent Publication JP1996-049091
(특허문헌 7) 일본공개특허공보 JP1997-202993호(Patent Document 7) JP1997-202993
(특허문헌 8) 한국출원특허 KR2012-0151505호(Patent Document 8) Korean Patent Application No. KR2012-0151505
(특허문헌 9) 한국출원특허 KR2012-0112818호(Patent Document 9) Korean Application Patent KR2012-0112818
본 발명의 일 측면은, 전기아연도금강판의 소지강판으로 사용되는 냉연강판 표면의 국부적인 성분 차이, 산화도의 차이에 기인하여 발생되는 전기아연도금강판의 도금 조직, 색상, 도금 두께 등의 불균일성을 제거할 수 있는 전기아연도금강판용 아연 플래쉬 도금 용액, 이를 이용한 전기아연도금강판의 제조방법과 그로부터 제조된 전기아연도금강판을 제공하고자 하는 것이다.One aspect of the present invention is the non-uniformity of the plating structure, color, plating thickness, etc. of the electro-zinc plated steel sheet generated due to the local component difference, the oxidation degree difference of the surface of the cold-rolled steel sheet used as the base steel sheet of the galvanized steel sheet It is to provide a zinc flash plating solution for an electrogalvanized steel sheet capable of removing the electroplated steel sheet, a method for producing an electrogalvanized steel sheet using the same and an electrogalvanized steel sheet prepared therefrom.
본 발명의 일 측면은, 아연(Zn) 이온, 아민계 유기화합물 및 기타 불가피한 불순물을 포함하는 표면외관이 우수한 전기아연도금강판용 아연 플래쉬 도금 용액을 제공한다.One aspect of the present invention provides a zinc flash plating solution for an electrogalvanized steel sheet having an excellent surface appearance including zinc (Zn) ions, amine organic compounds and other unavoidable impurities.
본 발명의 다른 일 측면은, 소지강판을 탈지 및 산세처리하는 단계; 상기 소지강판을 아연 플래쉬 도금 용액을 이용하여 아연 플래쉬 도금을 행하는 단계; 및 상기 아연 플래쉬 도금된 소지강판을 전기아연도금처리하는 단계를 포함하고, 상기 아연 플래쉬 도금 용액은 상술한 도금 용액을 이용하는 것인 표면외관이 우수한 전기아연도금강판의 제조방법과 이에 의해 제조된 전기아연도금강판을 제공한다.Another aspect of the invention, the step of degreasing and pickling the steel sheet; Performing zinc flash plating on the base steel sheet using a zinc flash plating solution; And electro-galvanizing the zinc flash-plated base steel sheet, wherein the zinc flash plating solution uses the above-described plating solution. Provide galvanized steel sheet.
본 발명에 따른 아연 플래쉬 도금 용액을 이용하여 아연 플래쉬 처리 후 전기아연도금을 행할 경우, 소지강판 즉, 냉연강판 표면의 성분 농화, 산화층의 불균일에 기인하여 발생되는 아연 도금 조직의 국부적인 불균일성 및 아연 도금층 두께 편차를 해소함으로써 표면외관이 우수한 전기아연도금강판을 제공할 수 있다.When performing zinc coating after zinc flash treatment using the zinc flash plating solution according to the present invention, localized nonuniformity of zinc plated structure and zinc due to the component thickening of the surface of the cold-rolled steel sheet, the nonuniformity of the oxide layer, and zinc By eliminating the thickness variation of the plating layer, it is possible to provide an electrogalvanized steel sheet having excellent surface appearance.
또한, 본 발명에 의해 제조된 전기아연도금강판은 자동차, 가전용 제품 등에 사용될 때, 도장 후 발생되는 요철성 결함 및 얼룩을 저감시키는 효과가 있다.In addition, the electro-galvanized steel sheet produced by the present invention, when used in automobiles, home appliances, etc., has the effect of reducing the irregularities and stains generated after coating.
뿐만 아니라, 본 발명에 따른 아연 플래쉬 도금 용액은 도금 효율이 높아 대량 생산을 위한 연속 전기도금공정에 적용하는데 적합하다.In addition, the zinc flash plating solution according to the present invention has a high plating efficiency and is suitable for application to a continuous electroplating process for mass production.
도 1은 본 발명의 실시예에서 발명예 1-1의 표면을 관찰한 결과를 나타낸 것이다.Figure 1 shows the results of observing the surface of the invention example 1-1 in the embodiment of the present invention.
도 2는 본 발명의 실시예에서 비교예 1-1의 표면을 관찰한 결과를 나타낸 것이다 (여기서 1은 표면에 발생된 얼룩을 표시한 것이다).Figure 2 shows the results of observing the surface of Comparative Example 1-1 in the embodiment of the present invention (where 1 represents a stain generated on the surface).
최근, 철강 제조 설비 및 기술이 발전함에 따라 냉연강판의 표면은 매우 청정하게 제조되어 그 표면품질이 엄격하게 관리됨에도 불구하고, 전기아연도금을 실시하는 경우 냉연강판 표면의 미세한 불균일성이 도금 표면에 다양한 형태의 얼룩과 결함이 발생되는 문제가 있다. Recently, with the development of steel manufacturing equipment and technology, the surface of the cold rolled steel sheet is manufactured very clean and the surface quality is strictly controlled. There is a problem that the shape of the spots and defects occur.
이에, 본 발명자들은 도금 전에 플래쉬 처리를 하지 않고 통상의 방법으로 탈지 및 산세를 실시하는 경우 아연도금강판 표면에 얼룩 및 도금 조직의 불균일성이 발생되는 원인을 확인하고, 이를 해결하기 위한 방법에 대해 깊이 연구하였다.Therefore, the present inventors have identified the cause of unevenness of plating and plating structure on the surface of the galvanized steel when degreasing and pickling in a conventional manner without flash treatment before plating, and the method for solving the problem Studied.
전기아연도금의 소지강판으로 사용되는 냉연강판은 수많은 열처리, 산세, 압연 공정을 통해 제조되는데, 이러한 제조 과정에서 강판의 표면에는 강 중에 함유된 미량 합금성분들이 국부적으로 농화되거나, 강판 표면의 산화층 두께에 미세한 편차가 발생하게 된다.Cold rolled steel sheet, which is used as a base steel sheet of electro-zinc plating, is manufactured through a number of heat treatment, pickling, and rolling processes. In this manufacturing process, trace alloy components contained in the steel are locally concentrated on the surface of the steel sheet, or the oxide layer thickness of the steel sheet surface. There is a slight deviation in.
위 냉연강판과 같은 소지강판에 행해지는 전기아연도금공정은 소지강판을 음극으로 하여 전기를 인가하면 도금 용액에 함유된 아연 이온이 환원되어 소지강판 표면에 석출되는 공정으로, 각각의 아연 이온이 소지강판 표면에 결정질의 금속으로 재배열되는 과정이다. 전기아연도금 중 아연 원자가 강판 표면에 재배열될 때, 아연 도금 입자의 방향은 소지강판 극표층의 철 원자 배열과 성분, 표면의 산화 수준에 의해 결정된다. 따라서, 강판 표면의 산화 수준이 낮고, 철 원자가 노출된 형태의 청정한 강판일수록 표면에서 아연이 석출될 때에 에피택시 성장을 하는 경향이 크게 나타난다. 그러므로, 강판 극표면의 미세한 차이는 아연도금조직의 배향, 입도에 직접적으로 영향을 주게 되어 도금 전의 소지강판에서는 그 차이가 미미하여 식별이 어렵더라도 아연도금 조직은 극명하게 차이가 발생하게 되고, 결과적으로 얼룩, 도금층의 두께 편차로 이어질 수 있다.Electro zinc plating process is carried out on the base steel sheet such as cold rolled steel sheet is a process in which the zinc ions contained in the plating solution is reduced and precipitated on the surface of the base steel sheet when electricity is applied using the base steel sheet as a cathode. It is the process of rearranging crystalline metal on the surface of steel sheet. When zinc atoms are re-arranged on the surface of the steel sheet in the galvanizing, the direction of the galvanized particles is determined by the arrangement of iron atoms in the pole surface layer of the steel sheet and the components and the oxidation level of the surface. Therefore, the lower the oxidation level of the surface of the steel sheet, the more clean steel sheet in the form of exposed iron atoms, the greater the tendency of epitaxy growth when zinc is deposited on the surface. Therefore, the minute difference of the pole surface of the steel plate directly affects the orientation and grain size of the galvanized structure, so that the difference is insignificant in the plated steel sheet before plating, so that the galvanized structure is obviously different. Unevenness may lead to thickness variation of the plating layer.
본 발명자들은 위와 같은 문제점을 근본적으로 해결하기 위하여, 소지강판에 전기아연도금을 행하기에 앞서 아연 플래쉬 도금을 먼저 행하는 경우, 통상의 전기아연도금을 행하더라도 균일한 외관을 갖는 전기아연도금강판을 제공할 수 있음을 확인하였다.In order to fundamentally solve the above problems, the inventors of the present invention, when the zinc flash plating prior to the electro-galvanizing of the base steel sheet, even if the electro-galvanization of ordinary galvanized steel sheet having a uniform appearance It was confirmed that it can be provided.
특히, 본 발명자들은 상기 아연 플래쉬 도금시 사용되는 도금 용액의 성분을 최적화하고, 이를 이용하여 아연 플래쉬 도금을 행한 결과, 냉연강판 표면의 성분 농화, 산화층의 불균일에 기인하여 발생되는 아연 도금 조직의 국부적인 불균일성 및 아연 도금층 두께 편차를 해소함으로써 표면외관이 우수한 전기아연도금강판을 얻을 수 있음을 확인하고, 본 발명을 완성하기에 이르렀다.In particular, the inventors of the present invention optimize the components of the plating solution used in the zinc flash plating, and by performing zinc flash plating using them, the localization of the galvanized structure caused by the concentration of components on the surface of the cold-rolled steel sheet, non-uniformity of the oxide layer By resolving the phosphorous nonuniformity and the thickness of the galvanized layer, it was confirmed that an electrogalvanized steel sheet having excellent surface appearance was obtained, and thus the present invention was completed.
이하, 본 발명에 대하여 상세히 설명한다.EMBODIMENT OF THE INVENTION Hereinafter, this invention is demonstrated in detail.
본 발명의 일 측면에 따른 전기아연도금강판용 아연 플래쉬 도금 용액은 아연(Zn) 이온, 아민계 유기화합물 및 기타 불가피한 불순물을 포함하는 것이 바람직하다.Zinc flash plating solution for an electrogalvanized steel sheet according to an aspect of the present invention preferably comprises zinc (Zn) ions, amine-based organic compounds and other unavoidable impurities.
보다 구체적으로, 상기 아연(Zn) 이온은 황산(SO4)계 또는 염산(HCl)계로서, 1~150g/L의 농도로 포함하는 것이 바람직하다.More specifically, the zinc (Zn) ions are sulfuric acid (SO 4 ) -based or hydrochloric acid (HCl) -based, preferably contained at a concentration of 1 ~ 150g / L.
상기 아연(Zn) 이온의 농도가 1g/L 미만이면 도금 효율이 저하되고 도금 가능한 최대 전류밀도인 한계전류밀도가 하락하여 고속전기도금 조업이 어려워지는 문제가 있다. 반면, 그 농도가 150g/L를 초과하게 되면 도금 용액에 함유된 아연 함량이 높아져 원료 가격이 상승하고, 용액 손실에 의한 Zn 낭비가 증가하게 되는 문제가 있다.When the concentration of zinc (Zn) ions is less than 1 g / L, the plating efficiency is lowered, and the limit current density, which is the maximum current density that can be plated, is lowered, thereby making it difficult to operate high-speed electroplating. On the other hand, if the concentration exceeds 150g / L, the zinc content in the plating solution is high, the raw material price is increased, there is a problem that Zn waste due to the solution loss is increased.
본 발명자들은 상기의 아연(Zn) 이온이 함유된 도금 용액에 다양한 형태의 유, 무기 화합물을 첨가해 보았으나, 첨가된 화합물이 강판 표면 및 도금층 표면에 지나치게 강한 결합을 하거나, 그 함량이 적정 수준을 초과하게 되면 후속하는 전기아연도금 중 아연의 석출이 억제되어 버닝 현상이 발생하여 도금 품질이 저하되는 문제가 있었으며, 반면 결합력이 너무 약하거나, 그 함량이 부족하게 되면 전기아연도금 후 양호한 외관을 얻을 수 없음을 확인하였다.The present inventors have tried to add various types of organic and inorganic compounds to the plating solution containing zinc (Zn) ions, but the added compound bonds too strongly to the surface of the steel sheet and the surface of the plating layer, or the content is appropriate. Exceeding the above resulted in the precipitation of zinc in the subsequent electro zinc plating is suppressed, the burning phenomenon occurs, the plating quality was deteriorated. On the other hand, if the bonding strength is too weak, or the content is insufficient, the appearance is good after electro zinc plating. It was confirmed that it could not be obtained.
한편, 아민계 유기화합물의 경우, 질소 원자에 포함된 비공유 전자쌍이 금속과 결합을 형성하게 되는데, 질소 원자와 결합된 탄화수소의 개수, 체인의 길이, 말단기에 따라 질소가 갖는 전자밀도가 달라진다. 예를 들어, 질소에 동일한 개수, 동일한 길이의 알킬보다는 알코올이 결합하게 되면 OH 기가 질소 원자 쪽으로 전자를 밀어내는 역할을 하기 때문에 이러한 아민 화합물은 상대적으로 금속 표면과 더 강한 흡착력을 갖게 된다. 다만, 질소와 결합된 탄화수소의 개수가 증가하면, 질소의 전자밀도는 증가할 수 있지만 탄소수소가 질소와 금속 표면의 결합을 방해하게 되므로 흡착력이 약화될 수 있다.On the other hand, in the case of the amine-based organic compound, the lone pair of electrons included in the nitrogen atom forms a bond with the metal, and the electron density of the nitrogen varies depending on the number of hydrocarbons, the chain length, and the end group bonded to the nitrogen atom. For example, when alcohols are bonded to nitrogen rather than the same number of alkyls of the same length, the amine group has a stronger adsorption force with the metal surface because the OH group acts to push electrons toward the nitrogen atom. However, when the number of hydrocarbons combined with nitrogen increases, the electron density of nitrogen may increase, but the adsorption force may be weakened because carbon hydrogen interferes with the bonding of nitrogen and the metal surface.
이에, 본 발명에서는 아연 플래쉬 도금 용액으로 상기 아연(Zn) 이온 이외에 소지강판과 아연도금층 표면에 용이하게 흡착하는 성질을 갖는 아민계 유기화합물을 포함하는 것이 바람직하며, 이것에 의해 다음과 같은 효과를 얻을 수 있다.Therefore, in the present invention, it is preferable that the zinc flash plating solution contains an amine-based organic compound having the property of easily adsorbing on the surface of the base steel sheet and the zinc plated layer, in addition to the zinc (Zn) ions. You can get it.
냉연강판 표면에 국부적인 산화도 차이 및 강 중에 함유된 성분들의 불균일한 농화는 전기아연도금 초기 단계에 아연(Zn) 이온이 석출되는 속도와 에피택시 성장하는 속도 간의 차이를 유발하게 되는데, 본 발명에서는 상기 아민계 화합물이 냉연강판 표면의 상태와 무관하게 강판 표면에 흡착됨으로써 전기아연도금 초기의 핵생성 속도를 균일하게 제어할 수 있게 된다.The difference in oxidation degree localized on the surface of the cold rolled steel and the nonuniform concentration of the components contained in the steel cause a difference between the rate of precipitation of zinc (Zn) ions and the rate of epitaxy growth in the early stage of electrogalvanization. In the amine-based compound is adsorbed on the surface of the steel sheet irrespective of the state of the cold-rolled steel sheet surface it is possible to uniformly control the nucleation rate of the initial electroplating.
또한, 냉연강판에 전기아연도금을 실시하는 경우, 아연도금의 핵은 도금 초기에만 형성되고, 도금이 진행되는 동안 아연은 핵 생성 없이 성장만 일어나는 경향이 있다. 즉, 전기아연도금 과정에서 2차 핵 생성이 일어나기 위해서는 통상의 수준보다 충분한 과전압을 인가하거나, 아연 도금이 충분히 진행되어 인가된 과전압 대비 아연의 성장속도가 둔화되는 상태에서 미미하게 발생하게 된다. 따라서, 통상의 전기아연도금조건에서 형성된 전기아연도금층의 조직 및 배향은 냉연강판이 가진 배향과 일정한 관계를 갖게 되며, 플래쉬 도금 수준의 극박 아연도금 시에는 냉연강판 조직 배향에 직접적으로 영향을 받게 된다.In addition, when electro-galvanizing the cold rolled steel sheet, the nuclei of zinc plating are formed only at the beginning of the plating, and during the plating, zinc tends to grow only without nucleation. That is, in order to generate secondary nucleation in the electro-zinc plating process, a sufficient overvoltage than a normal level is applied, or zinc plating is sufficiently progressed so that the growth rate of zinc is slowed down compared to the applied overvoltage. Therefore, the structure and orientation of the electro-galvanized layer formed under ordinary electro-zinc plating conditions have a certain relationship with the orientation of the cold-rolled steel sheet, and are directly affected by the orientation of the cold-rolled steel sheet during ultra-thin galvanizing at the level of flash plating. .
그러나, 아연 도금 표면에 쉽게 흡착되는 유기화합물을 첨가하게 되면, 초기 아연도금이 진행되는 동안 아연도금의 성장이 억제되어 연속적으로 핵 생성이 일어난다. 따라서, 아민계 유기화합물을 포함하는 도금 용액을 이용하게 되면, 냉연강판의 표면 상태에 무관하게 균일하고 미세한 아연 플래쉬 도금층을 형성할 수 있으며, 그 후 통상의 방법으로 전기아연도금을 실시하게 되면 외관이 균일한 전기아연도금강판을 제조할 수 있게 되는 것이다.However, when an organic compound that is easily adsorbed on the zinc plating surface is added, the growth of the zinc plating is suppressed during the initial galvanization, and nucleation is continuously performed. Therefore, by using a plating solution containing an amine-based organic compound, it is possible to form a uniform and fine zinc flash plating layer irrespective of the surface state of the cold rolled steel sheet. This uniform galvanized steel sheet can be produced.
그러므로, 본 발명의 전기아연도금강판용 아연 플래쉬 도금 용액은 아연(Zn) 이온 이외에 아민계 유기화합물을 포함함에 기술적 의의를 갖는다.Therefore, the zinc flash plating solution for electrogalvanized steel sheet of the present invention has a technical significance in that it contains an amine organic compound in addition to zinc (Zn) ions.
본 발명에서는 상기 아민계 유기화합물로서 1급 내지 3급 아민계 유기화합물을 이용하는 것이 유리하며, 보다 바람직하게 화합물 분자 내 질소 원자를 1개 이상 포함하고, 탄소수 1 내지 5의 체인 길이를 갖는 알리파틱(aliphatics) 구조의 질소 원자 1개당 탄화수소가 1 내지 3의 결합을 갖는 화합물 중에서 선택된 1종 또는 2종 이상의 혼합물인 것이 바람직하다.In the present invention, it is advantageous to use a primary to tertiary amine organic compound as the amine organic compound, more preferably an aliphatic containing at least one nitrogen atom in the compound molecule and having a chain length of 1 to 5 carbon atoms. It is preferable that the hydrocarbon per 1 nitrogen atom of an aliphatics structure is 1 type, or 2 or more types of mixtures chosen from the compound which has 1-3 bonds.
아민이 금속(소지강판)의 표면과 결합을 유지하기 위해서는 질소 원자에 비공유 전자쌍을 갖는 것이 좋다. 그러나, 4급 아민과 같이 질소 원자 1개당 탄화수소가 4개 결합되면, 질소의 비공유 전자쌍은 없고 양이온을 띄게 되는데, 이는 상대적으로 양이온을 형성하는 금속 표면과 정전기적 반발력을 띄게 되므로 금속 표면에 흡착이 불리해진다. 뿐만 아니라, 알리파틱 구조의 탄화수소로 결합된 4급 아민 화합물은 분자량이 증가할수록 수용액 내에서 용해도가 낮아져 용해가 불가능하거나 침전이 발생하는 문제가 있다.In order for an amine to maintain a bond with the surface of a metal (steel plate), it is preferable to have a lone pair of electrons at a nitrogen atom. However, when four hydrocarbons per nitrogen atom, like quaternary amines, are bonded, there are no lone pairs of nitrogen and they have a cation, which is relatively electrostatically repulsive with the cation-forming metal surface. Disadvantages. In addition, the quaternary amine compound bonded with a hydrocarbon having an aliphatic structure has a problem in that the solubility in the aqueous solution decreases as the molecular weight increases, so that dissolution is impossible or precipitation occurs.
또한, 상기의 1급 내지 3급의 아민계 유기화합물에 함유되는 탄화수소의 길이가 탄소수 5를 초과하면, 분자 내 질소가 차지하는 비율이 낮아 금속 표면에 흡착력이 약해지기 때문에 효과가 미미해진다.In addition, when the length of the hydrocarbon contained in the above-mentioned primary to tertiary amine organic compounds exceeds 5 carbon atoms, the ratio of nitrogen in the molecule is low, so that the effect of the adsorption is weak on the metal surface.
상기 아민계 유기화합물의 예로서, 화합물 분자 내 질소 원자를 1개 함유하는 1급 아민계 유기화합물로는 끓는 점이 높고, 수용액에 용해 가능한 에탄올아민(ethanolamine), 아미노 프로판올(amino propanol) 등의 아미노 알코올 중에서 선택될 수 있다. 또한, 분자 내 질소 원자를 1개 함유하는 2급 아민계 유기화합물로서 디에탄올아민(diethanolamine), 메틸에탄올아민(methylethanolamine) 등에서 선택될 수 있고, 분자 내 질소 원자를 1개 함유하는 3급 아민계 유기화합물로서 트리에틸아민(triethylamine), 디에틸아미노에탄올(diethylaminoethanol), 디에탄올에틸아민(diethanolethylamine), 트리에탄올아민(triethanolamine) 등에서 선택될 수 있다. 뿐만 아니라, 에틸렌디아민(ethylenediamine), 디에틸렌트리아민(diethylenetriamine), 트리에틸렌테트라민(triethylenetetramine), 디아미노프로판(diaminopropane), 스페르미딘(spermidine), 스페르민(spermine) 등의 선형 구조의 폴리 아민(polyamine), 사이클렌(cyclen, 1,4,7,10-tetraazacyclododecane), 사이클람(cyclam, 1,4,8,11-tetraazacyclotetradecane), 헥사메틸렌테트라민(hexamethylentetramine) 등 환형 또는 입체 구조의 수용성 폴리 아민 및 수용성 아민계 고분자 중에서 선택될 수 있다.As an example of the amine-based organic compound, the primary amine-based organic compound containing one nitrogen atom in the compound molecule has a high boiling point and is soluble in aqueous solution, such as ethanolamine or amino propanol. It can be selected from alcohols. In addition, as a secondary amine organic compound containing one nitrogen atom in the molecule, it can be selected from diethanolamine, methylethanolamine, etc., and tertiary amine system containing one nitrogen atom in the molecule. The organic compound may be selected from triethylamine, diethylaminoethanol, diethanolethylamine, triethanolamine, and the like. In addition, linear structures such as ethylenediamine, diethylenetriamine, triethylenetetramine, diaminopropane, spermidine, and spermine Cyclic or steric structures such as polyamine, cyclen (1,4,7,10-tetraazacyclododecane), cyclam (1,4,8,11-tetraazacyclotetradecane), hexamethylenetetramine (hexamethylentetramine) It can be selected from a water-soluble polyamine and a water-soluble amine polymer.
이중, 입체 구조의 수용성 폴리 아민 및 수용성 아민계 고분자는 질소 원자 수가 많고, 질소 원자의 비공유 전자쌍이 분자 바깥쪽으로 노출되어 있어, 금속과 결합할 수 있는 가능성이 높아 흡착이 용이해지므로, 전기아연도금강판의 표면을 개선하는데 보다 더 유리한 효과가 있다.Of these, three-dimensional water-soluble polyamines and water-soluble amine-based polymers have a large number of nitrogen atoms, and the non-covalent electron pairs of nitrogen atoms are exposed to the outside of the molecule, and thus have a high possibility of bonding with metal, thereby facilitating adsorption. There is a more beneficial effect on improving the surface of the steel sheet.
본 발명의 아민계 유기화합물은 상술한 아민계 화합물로 한정되는 것은 아니며, 1종의 아민계 유기화합물을 단독으로 사용하거나, 2종 이상을 혼합하여 사용할 수도 있다.The amine organic compound of the present invention is not limited to the amine compound described above, and may be used alone or in combination of two or more amine organic compounds.
이러한 아민계 유기화합물은 상기 도금 용액 내에 0.05~10g/L로 포함하는 것이 바람직하다. Such an amine organic compound is preferably contained in the plating solution at 0.05 ~ 10g / L.
만일, 아민계 유기화합물 농도가 도금 용액 1L 당 0.05g 미만이면 유기화합물이 금속 표면에 흡착되는 양이 적고, 도금 과정 중 유기화합물의 흡착 반응이 아연 석출 반응 대비 미미하게 되어 아연도금 후 외관 개선 효과가 크지 않다. 반면 10g을 초과하게 되면 유기화합물의 흡착이 과도하게 되어 아연 석출 반응을 억제하게 되므로 버닝 현상이 발생된다.If the concentration of the amine organic compound is less than 0.05 g per 1 L of the plating solution, the amount of the organic compound adsorbed on the metal surface is small, and the adsorption reaction of the organic compound during the plating process is less than that of the zinc precipitation reaction, thereby improving the appearance after galvanizing. Is not big. On the other hand, if the content exceeds 10g, the adsorption of the organic compound is excessive and the zinc precipitation reaction is suppressed, thereby causing a burning phenomenon.
상기와 같이, 아연(Zn) 이온과 아민계 유기화합물을 포함하는 본 발명의 전기아연도금강판용 아연 플래쉬 도금 용액은 1.0~5.0의 pH를 갖는 것이 바람직하다.As described above, the zinc flash plating solution for electro-galvanized steel sheet of the present invention containing zinc (Zn) ions and an amine organic compound preferably has a pH of 1.0 to 5.0.
만일, 아연 플래쉬 도금 용액의 pH가 1.0 미만이면 소지강판을 음극으로 하여 전기아연도금하는 과정에서 용액 내 수소의 환원 반응 속도가 증가하여 아연 도금의 석출량이 감소하고, 특히 저전류 도금시에는 아연이 석출되지 않는 문제가 발생한다. 반면, pH가 5.0을 초과하게 되면 아연 이온이나 소지강판으로부터 철 등의 불가피 불순물이 수산화물을 형성하면서 침전이 발생하는 문제가 있다.If the pH of the zinc flash plating solution is less than 1.0, the rate of reduction of hydrogen in the solution increases during electro-galvanizing of the base steel sheet as a cathode, thereby decreasing the amount of deposition of zinc plating. A problem that does not precipitate occurs. On the other hand, when the pH exceeds 5.0, there is a problem that precipitation occurs while inevitable impurities such as iron form hydroxides from zinc ions or steel sheets.
한편, 본 발명의 아연 플래쉬 도금 용액 내에는 전도도를 개선할 목적으로 황산나트륨, 황산칼륨, 황산암모늄, 염화칼륨 또는 염화나트륨 등의 지지염을 더 포함할 수 있다.Meanwhile, the zinc flash plating solution of the present invention may further include a supporting salt such as sodium sulfate, potassium sulfate, ammonium sulfate, potassium chloride or sodium chloride for the purpose of improving conductivity.
이때, 상기 지지염은 200g/L 이하로 함유됨이 바람직하며, 상기 범위 내로 지지염을 포함하더라도 아연 플래쉬 도금 후 전기아연도금하여 제조된 전기아연도금강판은 균일한 도금 외관을 가질 수 있다.At this time, the supporting salt is preferably contained in less than 200g / L, even if the supporting salt in the above range, the electro-galvanized steel sheet produced by electro-galvanizing after zinc flash plating may have a uniform plating appearance.
또한, 강판으로부터 용출되어 아연 플래쉬 도금 용액에 불가피하게 함유되는 철, 니켈, 망간 및 기타 불순물 이온의 침전을 억제하기 위하여 착화제를 더 포함할 수 있다.In addition, a complexing agent may be further included to suppress precipitation of iron, nickel, manganese and other impurity ions eluted from the steel sheet and inevitably contained in the zinc flash plating solution.
상기 착화제로는 예컨대 구연산, 구연산나트륨, 헵톤산나트륨 등을 이용할 수 있으며, 그 함량은 30g/L 이하인 것이 바람직하다. 상기 범위 내로 착화제를 포함하더라도 아연 플래쉬 도금 후 전기아연도금하여 제조된 전기아연도금강판은 균일한 도금 외관을 가질 수 있다. As the complexing agent, for example, citric acid, sodium citrate, sodium heptonate and the like can be used, and the content thereof is preferably 30 g / L or less. Even if the complexing agent is included in the above range, the galvanized steel sheet prepared by zinc plating after electroplating may have a uniform plating appearance.
상기 지지염 및 착화제는 본 발명의 아연 플래쉬 도금 용액에 선택적으로 첨가될 수 있는 것으로서, 이들 성분이 첨가되지 않더라도 제조되는 전기아연도금강판의 외관에 큰 영향을 미치지 않는다.The supporting salts and the complexing agents may be selectively added to the zinc flash plating solution of the present invention, and even if these components are not added, they do not significantly affect the appearance of the galvanized steel sheet produced.
이하에서는, 상술한 본 발명의 아연 플래쉬 도금 용액을 이용하여 전기아연도금강판을 제조하는 방법에 대하여 상세히 설명한다.Hereinafter, a method of manufacturing an electrogalvanized steel sheet using the zinc flash plating solution of the present invention described above will be described in detail.
먼저, 냉연강판을 통상적인 방법으로 탈지 및 산세 처리한 후, 아연 플래쉬 도금 및 전기아연도금을 순차적으로 실시하는 것이 바람직하다.First, after the cold rolled steel sheet is degreased and pickled in a conventional manner, it is preferable to sequentially perform zinc flash plating and electro zinc plating.
여기서, 소지강판으로 사용될 수 있는 강판은 특별히 제한되는 것은 아니며, 전기아연도금강판을 위한 어떠한 강판도 가능하나, 바람직하게는 냉연강판일 수 있다.Here, the steel sheet that can be used as the base steel sheet is not particularly limited, any steel sheet for the electro-galvanized steel sheet is possible, but preferably may be a cold-rolled steel sheet.
상기 아연 플래쉬 도금시 본 발명의 도금 용액을 이용하는 것이 바람직하며, 도금 용액의 온도를 상온(대략 25℃)~80℃로 조절하고, 전류밀도를 1~100A/dm2로 인가한 상태에서, 도금량이 10~2000mg/m2이 되도록 실시하는 것이 바람직하다.It is preferable to use the plating solution of the present invention when the zinc flash plating, and the plating amount in the state in which the temperature of the plating solution is adjusted to room temperature (approximately 25 ° C.) to 80 ° C. and the current density is applied at 1 to 100 A / dm 2 . It is preferable to carry out so that it may become 10-2000 mg / m <2> .
이때, 아연 플래쉬 도금 용액의 온도가 80℃를 초과하게 되면 용액 증발량이 과도해져 도금 용액의 관리가 어렵고, 작업 환경에 부식을 유발할 우려가 있다. 아연 플래쉬 도금 용액의 온도를 상온으로 유지하여도 도금 효과가 우수하나, 40~65℃로 유지하는 것이 도금 효율이 양호하고, 관리가 양호한 장점이 있으므로 보다 바람직하다.At this time, when the temperature of the zinc flash plating solution exceeds 80 ℃, the amount of solution evaporation is excessive, the management of the plating solution is difficult, there is a risk of causing corrosion in the working environment. Although the plating effect is excellent even if the temperature of the zinc flash plating solution is kept at room temperature, it is more preferable to maintain at 40 to 65 ° C because the plating efficiency is good and the management is good.
또한, 전류밀도가 1A/dm2 미만이면 도금 효율이 낮고, 적절한 수준의 아연 플래쉬 도금량을 얻기 위해서는 도금 시간이 장시간 소요되는 문제가 있어, 연속 도금 공정에서는 적절하지 못하다. 반면, 100A/dm2을 초과하는 경우에는 아연 플래쉬 도금 과정에서 버닝이 발생하여 얼룩을 유발하거나, 후속 전기아연도금 후 형성된 도금층의 밀착력이 불량해지는 문제가 있다.In addition, when the current density is less than 1A / dm 2, the plating efficiency is low, and in order to obtain an appropriate level of zinc flash plating amount, there is a problem that the plating takes a long time, which is not suitable in the continuous plating process. On the other hand, if it exceeds 100A / dm 2 there is a problem that burning occurs in the zinc flash plating process, causing stains, or poor adhesion of the plating layer formed after the subsequent electro-galvanization.
위와 같은 조건으로 아연 플래쉬 도금시, 아연 부착량은 10~2000mg/m2의 범위를 만족하도록 도금을 실시함이 바람직한데, 아연 부착량이 10mg/m2 미만이면 전기아연도금강판의 외관 개선 효과가 미미하고, 아연 플래쉬 도금된 소지강판을 후속하는 전기아연도금을 위해 산성의 전기아연도금용액과 접촉할 때 플래쉬 도금층이 국부적으로 용출되어 얼룩을 유발할 우려가 있다. 반면, 아연 부착량이 2000mg/m2를 초과하게 되면 전기아연도금강판의 외관 개선 효과는 양호하나, 아연 플래쉬 도금시 매우 고전류밀도가 적용되거나, 장시간 플래쉬 도금을 행하여야하므로, 생산성이 저하되어 경제적이지 못하다.In the case of zinc flash plating under the above conditions, it is preferable to perform plating so that the zinc adhesion amount satisfies the range of 10 to 2000 mg / m 2 , and when the zinc adhesion amount is less than 10 mg / m 2, the appearance improvement effect of the galvanized steel sheet is insignificant. In addition, when the zinc flash-plated base steel sheet is brought into contact with an acidic electrogalvanizing solution for subsequent electrogalvanization, the flash plating layer may be locally eluted to cause staining. On the other hand, when the zinc adhesion amount exceeds 2000 mg / m 2 , the appearance improvement effect of the galvanized steel sheet is good, but very high current density is applied when zinc flash plating is applied or flash plating is performed for a long time, so productivity is reduced and economical. Can not do it.
상기한 바에 따라, 아연 플래쉬 도금이 완료된 소지강판은 플래쉬 도금층을 포함하고 있으며, 이러한 소지강판에 전기아연도금을 행함으로써 5~100g/m2의 아연 부착량을 갖는 통상의 전기아연도금강판을 제조할 수 있다.As described above, the base steel sheet after zinc flash plating is completed includes a flash plating layer, and by performing electro zinc plating on the base steel sheet, a general electro galvanized steel sheet having a zinc adhesion amount of 5 to 100 g / m 2 can be produced. Can be.
본 발명에서 전기아연도금시 그 조건은 특별히 한정하지 아니하며, 통상 행해지는 조건 예컨대, 황산계 또는 염산계 전기아연도금욕에서 실시될 수 있다.In the present invention, the conditions of the electro-zinc plating are not particularly limited, and may be carried out in conditions which are usually performed, such as sulfuric acid or hydrochloric acid-based electro zinc plating baths.
상기 전기아연도금까지 완료하여 얻은 본 발명의 전기아연도금강판은 소지강판 상에 전기아연도금층을 포함하는 것으로, 표면외관이 우수한 특성을 갖는다.The electro-galvanized steel sheet of the present invention obtained by completing the above electro-zinc plating comprises an electro-galvanized layer on the base steel sheet, and has excellent surface appearance.
특히, 소지강판 상에 얼룩과 같은 결함이 존재하더라도, 전기아연도금 전에 본 발명에서 제안하는 아연 플래쉬 도금 용액을 이용하여 아연 플래쉬 도금을 행할 경우, 표면외관을 우수하게 확보할 수 있는 것이다.In particular, even if there are defects such as stains on the base steel sheet, when performing zinc flash plating using the zinc flash plating solution proposed in the present invention before electro-galvanizing, it is possible to ensure excellent surface appearance.
이하, 실시예를 통하여 본 발명을 보다 구체적으로 설명하고자 한다. 다만, 하기의 실시예는 본 발명을 예시하여 보다 상세하게 설명하기 위한 것일 뿐, 본 발명의 권리범위를 한정하기 위한 것이 아니라는 점에 유의할 필요가 있다. 본 발명의 권리범위는 특허청구범위에 기재된 사항과 이로부터 합리적으로 유추되는 사항에 의해 결정되는 것이기 때문이다.Hereinafter, the present invention will be described in more detail with reference to Examples. However, it is necessary to note that the following examples are only intended to illustrate the present invention in more detail, and are not intended to limit the scope of the present invention. This is because the scope of the present invention is determined by the matters described in the claims and the matters reasonably inferred therefrom.
(실시예 1) 전기아연도금강판의 제조Example 1 Preparation of Electro-Galvanized Steel Sheet
발명예 1Inventive Example 1
소지강판으로 냉연강판을 준비한 후, 이를 통상의 방법으로 알칼리 탈지 및 산세 처리한 다음, 순수를 이용하여 수세하였다.After preparing the cold rolled steel sheet to the base steel sheet, it was subjected to alkali degreasing and pickling treatment in a conventional manner, and then washed with pure water.
황산아연을 이용하여 아연(Zn) 이온 농도가 20~30g/L이 되도록 용해한 후, 여기에 아민계 유기화화합물인 에탄올아민과 헥사메틸테트라민을 혼합 및 용해하여 아연 플래쉬 도금 용액을 제조하였다. 이때, 상기 아민계 유기화합물은 그 총량이 용액 1L 당 중량으로 2.5~3.5g/L가 되도록 첨가하였다. 이후, 황산을 첨가하여 상기 아연 플래쉬 도금 용액의 pH가 1.5~2.5가 되도록 조절한 후, 45~55℃로 승온시켰다.After zinc zinc (Zn) ion concentration was dissolved using zinc sulfate so as to be 20-30 g / L, a zinc flash plating solution was prepared by mixing and dissolving an amine-based organic compound ethanolamine and hexamethyltetramine. At this time, the amine-based organic compound was added so that the total amount is 2.5 ~ 3.5g / L by weight per 1L solution. Thereafter, sulfuric acid was added to adjust the pH of the zinc flash plating solution to 1.5 to 2.5, and then heated to 45 to 55 ° C.
앞서 준비한 냉연강판을 승온시킨 아연 플래쉬 도금 용액에 1 초간 침지하여 아연 플래쉬 도금을 행하였으며, 도금 부착량이 50~2000mg/m2가 되도록 전류밀도를 제어하였으며, 그 결과 1.5~75A/dm2의 전류밀도가 인가되었다.Zinc flash plating was performed by immersing the prepared cold-rolled steel sheet in a heated zinc flash plating solution for 1 second. The current density was controlled so that the coating weight was 50 to 2000 mg / m 2 , and the current was 1.5 to 75 A / dm 2 . Density was applied.
상기에 따라 아연 플래쉬 도금된 냉연강판을 아연(Zn) 이온의 농도가 50~150g/L인 황산계 전기아연도금 용액에서 아연 도금 부착량이 20~40g/m2이 되도록 전기아연도금을 실시한 후, 순수를 이용하여 수세하여, 전기아연도금강판을 얻었다.After the zinc-plated cold-rolled steel sheet is subjected to electro-galvanization in a sulfuric acid-based galvanized solution having a zinc (Zn) ion concentration of 50-150 g / L, the zinc plating amount is 20-40 g / m 2 . Water was washed with pure water to obtain an electrogalvanized steel sheet.
발명예 2Inventive Example 2
상기 발명예 1과 동일한 아연 플래쉬 도금 용액에 지지염으로 황산나트륨을 100g/L, 착화제로 구연산을 10g/L 더 첨가하여 아연 플래쉬 도금 용액을 제조한 후 황산을 첨가하여 pH가 1.5~2.5가 되도록 조절한 후, 45~55℃로 승온시켰다.100 g / L of sodium sulfate as a supporting salt and 10 g / L of citric acid as a complexing agent were added to the same zinc flash plating solution as Inventive Example 1 to prepare a zinc flash plating solution, and then the sulfuric acid was added to adjust the pH to 1.5 to 2.5. After heating, the temperature was raised to 45 to 55 ° C.
상기 승온시킨 아연 플래쉬 도금 용액을 이용하여 상기 발명예 1과 동일한 냉연강판에 동일한 조건으로 아연 플래쉬 도금을 실시한 후 역시 동일한 조건으로 전기아연도금을 실시하여 전기아연도금강판을 얻었다.After the zinc flash plating solution was heated on the same cold rolled steel sheet as in Inventive Example 1 using the heated zinc flash plating solution, electrogalvanization was performed under the same conditions to obtain an electrogalvanized steel sheet.
비교예 1Comparative Example 1
상기 발명예 1과 동일하게 탈지 및 산세 처리한 후 수세처리된 냉연강판을 아연 플래쉬 도금 없이 바로 전기아연도금을 실시하여 전기아연도금강판을 얻었다.After degreasing and pickling in the same manner as in Inventive Example 1, the cold-rolled steel sheet washed with water was subjected to electro-galvanization without zinc flash plating to obtain an electro-galvanized steel sheet.
이때, 전기아연도금은 상기 발명예 1과 동일한 방법으로 실시하였다.At this time, the electrogalvanization was carried out in the same manner as in Example 1.
비교예 2Comparative Example 2
황산아연을 이용하여 아연(Zn) 이온 농도가 20~30g/L이 되도록 용해한 후, 황산을 첨가하여 용액의 pH가 1.5~2.5가 되도록 조절하여 아연 플래쉬 도금 용액을 제조하였다. 이후, 상기 아연 플래쉬 도금 용액을 45~55℃로 승온시켰다.Zinc (Zn) ion concentration was dissolved using zinc sulfate to 20 ~ 30g / L, and then sulfuric acid was added to adjust the pH of the solution to 1.5 ~ 2.5 to prepare a zinc flash plating solution. Then, the zinc flash plating solution was heated to 45 ~ 55 ℃.
상기 승온시킨 아연 플래쉬 도금 용액을 이용하여 상기 발명예 1과 동일한 냉연강판에 동일한 조건으로 아연 플래쉬 도금을 실시한 후 역시 동일한 조건으로 전기아연도금을 실시하여 전기아연도금강판을 얻었다.After the zinc flash plating solution was heated on the same cold rolled steel sheet as in Inventive Example 1 using the heated zinc flash plating solution, electrogalvanization was performed under the same conditions to obtain an electrogalvanized steel sheet.
비교예 3Comparative Example 3
황산아연을 이용하여 아연(Zn) 이온 농도가 20~30g/L이 되도록 용해한 후, 여기에 질소 함유 화합물인 티오우레아와 4급 아민계 유기화합물인 세틸트리메틸암모늄브로마이드 및 콜린 중 1종을 선택하여 혼합 및 용해하여 아연 플래쉬 도금 용액을 제조하였다. 이후, 황산을 첨가하여 상기 아연 플래쉬 도금 용액의 pH가 1.5~2.5가 되도록 조절한 후, 45~55℃로 승온시켰다.Using zinc sulfate, the zinc (Zn) ion was dissolved in a concentration of 20 to 30 g / L, and then one of the nitrogen-containing compound thiourea and the quaternary amine organic compound cetyltrimethylammonium bromide and choline was selected. Mixing and dissolving prepared a zinc flash plating solution. Thereafter, sulfuric acid was added to adjust the pH of the zinc flash plating solution to 1.5 to 2.5, and then heated to 45 to 55 ° C.
상기 승온시킨 아연 플래쉬 도금 용액을 이용하여 상기 발명예 1과 동일한 냉연강판에 동일한 조건으로 아연 플래쉬 도금을 실시한 후 역시 동일한 조건으로 전기아연도금을 실시하여 전기아연도금강판을 얻었다.After the zinc flash plating solution was heated on the same cold rolled steel sheet as in Inventive Example 1 using the heated zinc flash plating solution, electrogalvanization was performed under the same conditions to obtain an electrogalvanized steel sheet.
비교예 4Comparative Example 4
황산아연을 이용하여 아연(Zn) 이온 농도가 20~30g/L이 되도록 용해한 후, 여기에 아민계 유기화화합물인 에탄올아민과 헥사메틸테트라민을 혼합 및 용해하여 아연 플래쉬 도금 용액을 제조하였다. 이때, 상기 아민계 유기화합물은 그 총량이 용액 1L 당 중량으로 25~35g/L가 되도록 첨가하였다. 이후, 황산을 첨가하여 상기 아연 플래쉬 도금 용액의 pH가 1.5~2.5가 되도록 조절한 후, 45~55℃로 승온시켰다.After zinc zinc (Zn) ion concentration was dissolved using zinc sulfate so as to be 20-30 g / L, a zinc flash plating solution was prepared by mixing and dissolving an amine-based organic compound ethanolamine and hexamethyltetramine. At this time, the amine-based organic compound was added so that the total amount is 25 ~ 35g / L by weight per 1L solution. Thereafter, sulfuric acid was added to adjust the pH of the zinc flash plating solution to 1.5 to 2.5, and then heated to 45 to 55 ° C.
상기 승온시킨 아연 플래쉬 도금 용액을 이용하여 상기 발명예 1과 동일한 냉연강판에 동일한 조건으로 아연 플래쉬 도금을 실시한 후 역시 동일한 조건으로 전기아연도금을 실시하여 전기아연도금강판을 얻었다.After the zinc flash plating solution was heated on the same cold rolled steel sheet as in Inventive Example 1 using the heated zinc flash plating solution, electrogalvanization was performed under the same conditions to obtain an electrogalvanized steel sheet.
(실시예 2) 도금 외관 및 품질 평가(Example 2) Plating appearance and quality evaluation
상기 실시예 1에서 제조된 각각의 전기아연도금강판의 제품 외관에 대한 평가를 실시하고, 그 결과를 하기 표 1과 2에 나타내었다.Evaluation of the product appearance of each of the galvanized steel sheet produced in Example 1, the results are shown in Tables 1 and 2.
냉연강판 표면은 제조 방법에 따라 상대적으로 매우 균일한 소재가 제공될 수도 있다. 그러나, 전기아연도금을 실시하기 전에는 냉연강판의 표면을 조사하여 얼룩 발생 여부를 예상하기 어려우므로, 냉연강판에 아연 플래쉬 도금을 실시하지 않고 통상의 탈지, 산세만을 거친 냉연강판에 전기아연도금을 바로 실시하여 얼룩 발생 여부를 우선적으로 확인하였으며, 이와 동일한 냉연강판을 채취하여 소지강판으로 사용하였다.The cold rolled steel surface may be provided with a relatively very uniform material depending on the manufacturing method. However, since the surface of the cold rolled steel sheet is difficult to predict whether staining occurs before the electro-galvanizing is performed, the electro-galvanized steel sheet is directly applied to the cold rolled steel sheet subjected to normal degreasing and pickling only without performing zinc flash plating on the cold rolled steel sheet. First, the occurrence of stains was checked first, and the same cold rolled steel was taken and used as a holding steel sheet.
냉연강판 표면의 불균일성에 기인한 전기아연도금강판 표면의 얼룩은 육안으로 확인이 가능하다. 이에, 아연 플래쉬 도금에 따른 개선 여부는 전기아연도금을 실시한 후 얼룩 발생 여부를 육안으로 확인하였다. 얼룩 발생 수준은 다음과 같은 기준으로 등급을 설정하였다.Unevenness of the surface of the galvanized steel sheet due to the nonuniformity of the surface of the cold rolled steel sheet can be visually confirmed. Thus, whether the improvement according to the zinc flash plating was confirmed visually whether the stain after the electro-galvanization. The stain generation level was set based on the following criteria.
○: 육안으로 얼룩이 뚜렷하게 확인되며, 현미경 관찰시 도금 조직 차이가 명확함○: The stain is clearly seen by the naked eye, and the difference in plating structure is apparent when the microscope is observed.
△: 육안으로 미세하게 얼룩이 있으나, 현미경 관찰시 도금 조직 차이가 크지 않음(Triangle | delta): Although it is finely stained with the naked eye, when a microscope observes, a plated structure difference does not become large
×: 육안으로 식별하기 어려움×: Difficult to identify visually
전기아연도금강판의 표면에 발생되는 국부적인 얼룩 이외에도 소지강판의 미량 합금 성분, 제조 조건, 코일별에 따라 전기아연도금강판의 색상 차이가 발생될 수 있다. 자동차용 또는 PCM 강판용 전기도금강판의 경우 아연도금강판에 도장을 실시하여 사용하므로 코일별 색상 차이는 품질 특성에 큰 영향을 주지 않지만, 가전용 내지문 강판은 그 색상을 일정하게 유지될 필요가 있다.In addition to the local stains generated on the surface of the galvanized steel sheet, the color difference of the electrogalvanized steel sheet may be generated depending on the trace alloy component, manufacturing conditions, and coils of the base steel sheet. In the case of electroplated steel sheet for automotive or PCM steel sheet, the galvanized steel sheet is used for painting, so the color difference of each coil does not affect the quality characteristics, but for home appliance steel plate, the color needs to be kept constant. .
따라서, Mn 및 Al 함량의 합이 600ppm 내지 1300ppm을 함유하는 4종의 냉연 코일(그외 성분은 동일)에 대하여 하기 표 1, 2에 나타낸 각각의 조건으로 아연 플래쉬 도금 처리/미처리한 후 동일 조건에서 전기도금을 실시한 후 각 시편별로 3점에 대하여 D65 광원, 수광각 8o, 시야각 10o의 조건으로 색상을 측정하고 총 12점의 평균 백색도를 산출하였다.Therefore, four kinds of cold-rolled coils (the other components being the same) containing a sum of Mn and Al content of 600 ppm to 1300 ppm were subjected to zinc flash plating treatment / untreatment under the respective conditions shown in Tables 1 and 2 below. After electroplating, the color was measured under the conditions of D65 light source, light receiving angle 8 o , and viewing angle 10 o for three samples for each specimen, and the average whiteness of 12 points was calculated.
또한 아연도금강판에서 얼룩은 색상과 도금 조직의 불균일성에 기인하므로, 얼룩 발생 수준을 정량적으로 비교하기 위해 동일 조건에서 제조하여 측정된 12점의 평균 색상을 기준으로 색차를 계산하고 색차의 제곱 평균의 제곱근으로 색상 편차로 산출하였다. In addition, since staining is caused by unevenness of color and plating texture in galvanized steel sheet, the color difference is calculated based on the average color of 12 points manufactured and measured under the same conditions in order to quantitatively compare the level of staining. Calculated as color deviation with square root.
구분division 아연 플래쉬 도금 용액Zinc flash plating solution 도금량Plating amount 품질 평가Quality evaluation
Zn 이온(g/L)Zn ion (g / L) pHpH 첨가제 성분 및 농도Additive Ingredients and Concentrations 온도(℃)Temperature (℃) 플래쉬 도금(mg/m2)Flash plating (mg / m 2) 전기아연도금(g/m2)Electro zinc plating (g / m 2 ) 얼룩 발생 수준Spotting Level 평균백색도Average whiteness 색상편차Color deviation
발명예 1-1Inventive Example 1-1 2525 22 1급 및 3급의 수용성 아민2.5~3.5g/LPrimary and tertiary water-soluble amines 2.5 to 3.5 g / L 5050 5050 2020 ×× 87.8087.80 0.260.26
발명예 1-2Inventive Example 1-2 500500 ×× 88.2388.23 0.190.19
발명예 1-3Inventive Example 1-3 10001000 ×× 87.4987.49 0.210.21
발명예 1-4Inventive Example 1-4 20002000 ×× 88.1488.14 0.270.27
발명예 1-5Inventive Example 1-5 5050 4040 ×× 87.1387.13 0.240.24
발명예 1-6Inventive Example 1-6 500500 ×× 87.3787.37 0.210.21
발명예 1-7Inventive Example 1-7 10001000 ×× 86.9786.97 0.120.12
발명예 1-8Inventive Example 1-8 20002000 ×× 86.6886.68 0.270.27
발명예 2-1Inventive Example 2-1 2525 22 1급 및 3급의 수용성 아민 2.5~3.5g/L,황산나트륨 100g/L및구연산10g/LPrimary and tertiary water-soluble amines 2.5 to 3.5 g / L, sodium sulfate 100 g / L and citric acid 10 g / L 5050 5050 2020 ×× 86.7686.76 0.480.48
발명예 2-2Inventive Example 2-2 500500 ×× 86.7886.78 0.390.39
발명예 2-3Inventive Example 2-3 10001000 ×× 86.9986.99 0.230.23
발명예 2-4Inventive Example 2-4 20002000 ×× 86.3686.36 0.520.52
발명예 2-5Inventive Example 2-5 5050 4040 ×× 86.4386.43 0.440.44
발명예 2-6Inventive Example 2-6 500500 ×× 86.5586.55 0.240.24
발명예 2-7Inventive Example 2-7 10001000 ×× 86.1786.17 0.300.30
발명예 2-8Inventive Example 2-8 20002000 ×× 86.3086.30 0.380.38
구분division 아연 플래쉬 도금 용액Zinc flash plating solution 도금량Plating amount 품질 평가Quality evaluation
Zn 이온(g/L)Zn ion (g / L) pHpH 첨가제 성분 및 농도Additive Ingredients and Concentrations 온도(℃)Temperature (℃) 플래쉬 도금(mg/m2)Flash Plating (mg / m 2 ) 전기아연도금(g/m2)Electro zinc plating (g / m 2 ) 얼룩 발생 수준Spotting Level 평균 백색도Average whiteness 색상편차Color deviation
비교예 1-1Comparative Example 1-1 -- -- -- -- 미실시Not carried 2020 84.4984.49 2.562.56
비교예 1-2Comparative Example 1-2 4040 83.5783.57 2.572.57
비교예 2-1Comparative Example 2-1 2525 22 -- 5050 5050 2020 85.3985.39 3.753.75
비교예 2-2Comparative Example 2-2 500500 85.6985.69 3.243.24
비교예 2-3Comparative Example 2-3 10001000 85.0485.04 3.163.16
비교예 2-4Comparative Example 2-4 20002000 84.9984.99 2.982.98
비교예 3-1Comparative Example 3-1 2525 22 티오우레아3.8g/LThiourea3.8g / L 5050 5050 2020 84.1484.14 1.521.52
비교예 3-2Comparative Example 3-2 500500 84.2384.23 1.041.04
비교예 3-3Comparative Example 3-3 10001000 ×× 84.1584.15 0.920.92
비교예 3-4Comparative Example 3-4 20002000 ×× 84.4184.41 0.870.87
비교예 3-5Comparative Example 3-5 2525 22 세틸트리메틸암모늄브로마이드1.8g/LCetyltrimethylammonium bromide1.8g / L 5050 5050 2020 84.4884.48 1.251.25
비교예 3-6Comparative Example 3-6 500500 83.6783.67 1.731.73
비교예 3-7Comparative Example 3-7 10001000 ×× 84.1684.16 1.111.11
비교예 3-8Comparative Example 3-8 20002000 ×× 84.5484.54 0.940.94
비교예 3-9Comparative Example 3-9 2525 22 염화콜린7.0g/LCholine chloride7.0g / L 5050 5050 2020 84.1584.15 1.521.52
비교예 3-10Comparative Example 3-10 500500 83.9983.99 1.541.54
비교예 3-11Comparative Example 3-11 10001000 84.4084.40 1.671.67
비교예 3-12Comparative Example 3-12 20002000 83.7583.75 1.531.53
비교예 4-1Comparative Example 4-1 2525 22 1급 및 3급의 수용성 아민25~35g/LPrimary and tertiary water-soluble amines 25 to 35 g / L 5050 5050 2020 87.6187.61 0.490.49
비교예 4-2Comparative Example 4-2 500500 87.9787.97 0.480.48
비교예 4-3Comparative Example 4-3 10001000 87.4687.46 0.230.23
비교예 4-4Comparative Example 4-4 20002000 87.2587.25 0.280.28
상기 표 1에 나타낸 바와 같이, 본 발명에서 제공하는 아연 플래쉬 도금 용액을 이용하여 플래쉬 도금을 행한 후 전기아연도금을 행하는 경우, 모든 경우에서 냉연강판 표면의 불균일성에 기인한 얼룩을 육안으로 식별할 수 없었으며, 평균 백색도가 86 내지 89 수준으로 매우 높았다.As shown in Table 1, when electro-galvanizing after the flash plating using the zinc flash plating solution provided in the present invention, in all cases, stains due to nonuniformity of the surface of the cold rolled steel sheet can be visually identified. There was no average whiteness of 86-89.
또한, 서로 다른 냉연강판을 사용하여 전기아연도금강판을 제조하더라도 색상 편차가 0.5 미만으로, 표면 외관이 균일하여 식별이 어려운 수준이었다.In addition, even when the electro-galvanized steel sheet was manufactured using different cold-rolled steel sheets, the color deviation was less than 0.5, and the surface appearance was uniform, which made it difficult to identify.
또한, 아연 플래쉬 도금시 부착량은 전기아연도금강판의 외관에 큰 영향을 미치지 않음을 확인할 수 있었으며, 아연 플래쉬 도금 용액에 지지염, 착화제를 더 포함하더라도 전기아연도금강판의 표편 품질은 유사한 수준을 얻을 수 있었다.In addition, it was confirmed that the adhesion amount during zinc flash plating did not have a significant effect on the appearance of the galvanized steel sheet, and even though the zinc flash plating solution further contained supporting salts and complexing agents, the surface quality of the galvanized steel sheet was similar. Could get
이와 같은 결과는 아연 플래쉬 도금층이 도금 초기에 형성될 때, 소지강판 표면 상태에 무관하게 일정한 수준의 입도와 배향을 갖고 형성되고, 이후 전기아연도금을 실시할 때 동일한 표면의 아연 플래쉬 도금층 위에 아연이 석출되기 때문에 결과적으로 강판 표면 상태의 불균일성 및 코일 종류에 무관하게 동일한 외관과 조직을 갖게 됨을 보여주는 것이다.This result shows that when the zinc flash plating layer is formed at the beginning of plating, it is formed with a certain level of particle size and orientation irrespective of the surface state of the base steel sheet, and then zinc is deposited on the zinc flash plating layer on the same surface when electrogalvanizing is performed. Precipitation results in the same appearance and structure regardless of the type of coil and the nonuniformity of the surface of the steel sheet.
반면, 표 2에 나타낸 바와 같이, 아연 플래쉬 도금을 행하지 않고 전기아연도금만을 행한 비교예 1-1 내지 1-2의 경우에는 표면에 줄무늬 형태의 심한 얼룩이 육안으로 쉽게 관찰되었으며, 현미경으로 도금 조직으로 확인해본 결과 도금 조직이 국부적으로 불균일한 것을 확인할 수 있었다.On the other hand, as shown in Table 2, in the case of Comparative Examples 1-1 to 1-2 where only the electro-zinc plating was performed without zinc flash plating, severe stains in the form of stripes on the surface were easily observed with the naked eye. As a result, it was confirmed that the plating structure was locally nonuniform.
또한, 아연 플래쉬 처리한 경우보다 백색도가 평균적으로 2~3 수준 낮았으며, 서로 다른 냉연강판으로부터 도금된 전기아연도금강판에서 색상 편차가 2.5~4.0 수준으로 측정되었다. 이는, 냉연강판 표면의 미세한 차이가 전기도금 후 표면의 색상에 큰 영향을 주는 것을 보여주는 것이다. 일반적으로 색차가 2.0 이상인 경우 두 색의 차이를 육안으로 쉽게 판단할 수 있는 수준으로 알려져 있는데, 색상 편차가 최소 2.5 이상으로 색상 차이를 쉽게 인지할 수 있는 수준이 되므로 균일한 제품생산이 어렵게 된다.In addition, the average whiteness was 2 to 3 levels lower than the zinc flash treatment, and the color deviation was measured to be 2.5 to 4.0 in the galvanized steel sheets plated from different cold rolled steel sheets. This shows that the minute difference of the surface of the cold rolled steel sheet has a great influence on the color of the surface after electroplating. In general, when the color difference is 2.0 or more, it is known that the difference between the two colors can be easily determined by the naked eye. Since the color deviation is at least 2.5 or more, the color difference becomes easily recognizable, making it difficult to produce a uniform product.
아연 플래쉬 도금은 행하였으나, 그 도금 용액 내 아민계 유기화합물을 전혀 포함하지 않은 비교예 2-1 내지 2-4의 경우에는 비교예 1-1 및 1-2에 비해서는 백색도가 소폭 증가하였으나, 표면 얼룩은 쉽게 판별이 가능한 정도였다. Although zinc flash plating was carried out, in the case of Comparative Examples 2-1 to 2-4 which did not contain any amine organic compound in the plating solution, the whiteness was slightly increased compared to Comparative Examples 1-1 and 1-2, Surface stains were easily discernible.
또한, 냉연강판 종류에 따른 색상 편차는 오히려 더 증가하는 경향을 보였는데, 이는 통상적인 전기아연도금용액 대비 비교적 아연 농도가 낮고, pH가 높은 플래쉬 도금 용액으로 도금을 행함으로써 농도와 pH 차이에 의해 도금 초기의 핵 생성 빈도에 영향을 준 것으로 보이나, 냉연강판 표면의 차이 또는 불균일성이 전기아연도금 과정에서 더 가중되어 전사된 것으로 볼 수 있다.In addition, the color variation according to the type of cold rolled steel tended to increase more, which is due to the difference in concentration and pH by plating with a flash plating solution having a relatively low zinc concentration and a high pH compared to a conventional electrogalvanizing solution. It seems to have influenced the frequency of nucleation at the initial stage of plating, but the difference or nonuniformity of the surface of cold rolled steel sheet could be considered to be more weighted and transferred during the galvanizing process.
다양한 아민계 화합물을 첨가한 도금 용액으로 아연 플래쉬 도금을 행한 후 전기아연도금강판을 제조한 비교예 3-1 내지 3-12의 경우에 대한 결과는 다음과 같다.Results of the case of Comparative Examples 3-1 to 3-12 in which zinc flash plating was performed with a plating solution to which various amine-based compounds were added, followed by producing an electrogalvanized steel sheet were as follows.
먼저, 4급 아민계 화합물인 염화콜린을 첨가하여 아연 플래쉬 도금을 행한 비교예 3-9 내지 3-12의 경우에는 색상 편차가 소폭 개선되었지만, 표면 얼룩은 쉽게 확인되었다. 이는 콜린 분자에 의해 도금 과전압 변화, 도금입자의 성장속도에 영향을 주어 핵 생성 빈도 및 도금 입도에 미세한 차이를 유발하기 때문으로 판단되나, 결과적으로 냉연강판 표면의 불균일성은 전기아연도금 후까지 전사되어 개선 효과는 미미한 것으로 판단된다.First, in Comparative Examples 3-9 to 3-12 in which zinc flash plating was performed by adding choline chloride, a quaternary amine compound, color variation was slightly improved, but surface staining was easily confirmed. This is because choline molecules affect the plating overvoltage change and the growth rate of the plated particles, causing small differences in the frequency of nucleation and the particle size.However, the non-uniformity of the surface of the cold rolled steel sheet is transferred until after electro-galvanization. The improvement seems to be minimal.
한편, 티오우레아를 첨가제로 사용한 비교예 3-1 내지 3-4의 경우에는 전기아연도금강판 표면의 얼룩이 상당히 개선되는 효과가 있었고, 광택도 증가하였다. 또한 비교예 1 또는 2에 비해 색상 편차가 현저히 감소하였다. 그러나, 티오우레아 대신 우레아를 사용하는 경우에는 비교예 2-1 내지 2-4와 동일한 결과를 얻었다. 우레아는 티오우레아와 그 분자구조가 동일하나 티오우레아의 황 원자 대신 산소 원자로 구성된 아미드 화합물이다. 따라서, 아미드 화합물은 아민 화합물과 달리 전기도금 강판의 외관을 개선하는데 큰 효과가 없으며, 티오우레아와 같이 황을 함유하는 화합물의 경우, 황에 의한 표면 흡착 효과 때문에 제품 외관 개선 효과가 있는 것으로 판단된다. 하지만, 티오우레아와 같은 황을 함유하는 분자는 양극에서 쉽게 전기 분해되므로 도금이 진행됨에 따라 백색의 침전물이 발생하여 연속 전기아연도금공정에는 적절하지 않았다.On the other hand, in the case of Comparative Examples 3-1 to 3-4 using thiourea as an additive, there was an effect that the stain of the surface of the galvanized steel sheet was significantly improved, the gloss also increased. In addition, the color deviation was significantly reduced compared to Comparative Example 1 or 2. However, when urea was used instead of thiourea, the same results as in Comparative Examples 2-1 to 2-4 were obtained. Urea is an amide compound having the same molecular structure as thiourea but consisting of oxygen atoms instead of sulfur atoms of thiourea. Therefore, unlike the amine compound, the amide compound does not have a significant effect on improving the appearance of the electroplated steel sheet, and in the case of a compound containing sulfur such as thiourea, it is believed that the amide compound has an improvement in product appearance due to the surface adsorption effect by sulfur. . However, since sulfur-containing molecules such as thiourea are easily electrolyzed at the anode, a white precipitate occurs as the plating proceeds, which is not suitable for the continuous electrogalvanization process.
세틸트리메틸암모늄브로마이드는 계면활성제의 일종으로, 콜린과 마찬가지로 4급 아민계 화합물이다. 이러한 화합물을 첨가제로 사용한 비교예 3-5 내지 3-8의 경우, 티오우레아와 유사한 수준의 효과가 나타났다. 이러한 결과는 콜린 분자의 경우 소수기와 친수기로 구분되는 계면활성제가 아니므로 분자가 강판 또는 아연 금속 표면에 흡착되려는 성질이 약한 반면, 세틸트리메틸암모늄은 소수성 영역과 친수성 영역이 구분되는 계면활성제이므로 수용액과 강판의 계면에 배열되려는 성향이 강하기 때문이며, 아민에 의한 금속 표면 흡착에 의한 효과는 아닌 것으로 판단된다. 또한, 브롬과 같은 할라이드 이온을 함유하고 있으므로 과전압이 높은 고속의 전기아연도금공정 중에는 할라이드 기체가 발생할 가능성이 높은 우려가 있다.Cetyltrimethylammonium bromide is a kind of surfactant and is a quaternary amine compound like choline. For Comparative Examples 3-5 to 3-8 using these compounds as additives, similar effects to thiourea were seen. These results indicate that choline molecules are not surfactants classified as hydrophobic groups and hydrophilic groups, and thus the molecules are weakly adsorbed on the steel sheet or zinc metal surface, whereas cetyltrimethylammonium is a surfactant that distinguishes hydrophobic and hydrophilic regions, so It is because the tendency to arrange | position at the interface of a steel plate is strong, and it is judged that it is not an effect by metal surface adsorption by an amine. In addition, since halide ions such as bromine are contained, there is a high possibility that halide gas is generated during the high-speed electrozinc plating process with high overvoltage.
이외에도 4급 아민 고분자 화합물을 1g/L 이하로 첨가하고자 하였으나, 산성 아연도금용액에서 침전이 발생하여 전기아연도금이 불가하였다.In addition, the quaternary amine polymer compound was to be added below 1 g / L, but electro zinc coating was not possible because precipitation occurred in the acidic zinc plating solution.
상기 발명예 1과 동일한 첨가제를 이용하여 아연 플래쉬 도금을 행하였으나, 그 함량이 너무 과도한 비교예 4-1 내지 4-4의 경우에는, 전류가 집중되는 시편의 가장 자리 영역에서 아연 도금층이 검게 변하는 버닝 현상을 확인할 수 있었다. 여기서, 버닝 현상은 평활 도금이 가능한 임계 도금속도를 초과하는 경우, 도금층에 수산화물이 혼입되고 평활 도금이 이루어지지 않아 검게 변하는 현상을 말한다.Zinc flash plating was carried out using the same additive as inventive example 1, but in Comparative Examples 4-1 to 4-4 in which the content was too high, the zinc plating layer turned black in the edge region of the specimen where the current was concentrated. Burning phenomenon could be confirmed. Here, the burning phenomenon refers to a phenomenon in which hydroxide is mixed in the plating layer and blackening occurs because smooth plating is not performed when the plating speed exceeds a critical plating speed.
이 중, 아연 플래쉬 도금을 50mg/m2 수준으로 도금하기 위해 전류밀도를 약 1.5A/dm2 수준으로 적용한 비교예 4-1의 경우, 시편 가장자리에서 버닝 현상이 계속 발생하였으나, 시편의 중앙 부분은 얼룩이 없고, 색상 편차가 적은 전기아연도금강판을 제조할 수 있었다. 따라서, 이들 강판 표면에서 관찰되는 표면 얼룩은 냉연강판 표면의 불균일성에 기인한 얼룩이 아니며, 전기아연도금공정 중 발생한 시편 가장자리의 버닝에 의한 얼룩 발생을 나타낸 것이다.Among them, in the case of Comparative Example 4-1 in which the current density was applied at about 1.5 A / dm 2 level to plate the zinc flash plating at 50 mg / m 2 level, the burning phenomenon continued at the edge of the specimen. It was possible to produce an electrogalvanized steel sheet having no silver stain and less color variation. Therefore, the surface unevenness observed on the surface of these steel sheets is not due to unevenness of the surface of the cold rolled steel sheet, but shows unevenness due to the burning of the specimen edges generated during the galvanizing process.
실제로 전기아연도금강판 제조 공정시 유속에 의한 교반이 높고 용액 중 아연의 함량이 높은 경우에는 버닝 현상에 대한 개선 효과를 기대할 수 있으나, 가장 자리의 전류 집중은 오히려 가중되기 때문에 강판의 가장자리를 잘라내는 트리밍 작업이 추가되어야만 한다.In fact, in the manufacturing process of the galvanized steel sheet, if the agitation due to the flow rate is high and the zinc content in the solution is high, an improvement effect on the burning phenomenon can be expected, but since the current concentration at the edge is rather weighted, the edge of the steel sheet is cut out. Trimming operations must be added.
뿐만 아니라, 첨가제 량이 많을수록 용액의 단가는 상승하게 되고, 도금 효율은 저하되므로 첨가제 즉, 아민 유기화합물을 적절한 수준을 유지하면서 가급적 적게 함유하는 것이 바람직하다.In addition, as the amount of the additive increases, the unit cost of the solution increases and the plating efficiency decreases. Therefore, it is preferable to contain the additive, that is, the amine organic compound as little as possible while maintaining an appropriate level.
통상적으로 첨가제를 함유하지 않은 전기아연도금용액에서 강판에 순수한 아연을 전기도금한 경우, 소지강판과 도금층의 밀착성이 매우 우수하다. 그러나, 전기아연도금 전에 첨가제가 함유된 아연 플래쉬 용액으로 플래쉬 처리를 하게 되면, 도금층과 소지강판의 밀착성이 저하될 수 있다. 따라서, 도금층과 소지강판의 밀착성을 평가하기 위해 강판을 곡률반경이 0.5mm인 금형을 이용하여 90o로 굽힌 후 굽힘부의 안쪽을 테이프로 박리시켜 소지철과 아연도금층의 밀착성을 평가하였다. Usually, when pure zinc is electroplated on a steel sheet in an electrogalvanized solution containing no additives, the adhesion between the base steel sheet and the plating layer is very excellent. However, when the flash treatment is performed with a zinc flash solution containing an additive before electro-galvanizing, adhesion between the plating layer and the base steel sheet may be degraded. Therefore, in order to evaluate the adhesion between the plated layer and the base steel sheet, the steel sheet was bent to 90 ° using a mold having a radius of curvature of 0.5 mm, and then the inside of the bent portion was peeled off with a tape to evaluate the adhesion between the base steel and the zinc plated layer.
평가결과, 모든 실시예(발명예 1과 2, 비교예 1 내지 4)의 전기아연도금강판에서 소지철과 아연도금층의 박리가 발생하지 않고 밀착성이 양호하였다.As a result of evaluation, in the electrogalvanized steel sheets of all the examples (Invention Examples 1 and 2, Comparative Examples 1 to 4), peeling of the base iron and the zinc plated layer did not occur, and adhesion was good.
도 1과 도 2는 각각의 발명예 1-1과 비교예 1-1의 전기아연도금강판의 표면을 나타낸 것이다.1 and 2 show the surfaces of the electrogalvanized steel sheets of Inventive Example 1-1 and Comparative Example 1-1, respectively.
도면으로부터 확인할 수 있는 바와 같이, 아연 플래쉬 도금을 행하지 아니한 비교예의 경우에는 최종 제품(전기아연도금강판) 표면에 얼룩이 육안으로 명백히 확인되는 것을 볼 수 있으나, 동일 소지강판에 본 발명에 따라 아연 플래쉬 도금을 행한 후 전기아연도금하여 얻은 전기아연도금강판은 표면외관이 매우 우수하였다.As can be seen from the drawings, in the case of the comparative example without performing the zinc flash plating, it can be seen that the stain on the surface of the final product (electro galvanized steel) is clearly visible, but zinc flash plating according to the present invention on the same steel sheet After the galvannealing, the electrogalvanized steel sheet was very excellent in surface appearance.

Claims (10)

  1. 아연(Zn) 이온, 아민계 유기화합물 및 기타 불가피한 불순물을 포함하는 표면외관이 우수한 전기아연도금강판용 아연 플래쉬 도금 용액.Zinc flash plating solution for electro-galvanized steel sheet with excellent surface appearance including zinc (Zn) ions, amine organic compounds and other unavoidable impurities.
  2. 제 1항에 있어서,The method of claim 1,
    상기 아연(Zn) 이온은 1~150g/L의 농도로 포함하는 것인 표면외관이 우수한 전기아연도금강판용 아연 플래쉬 도금 용액.The zinc (Zn) ions zinc flash plating solution for an electro-zinc plated steel sheet having an excellent surface appearance that contains at a concentration of 1 ~ 150g / L.
  3. 제 1항에 있어서,The method of claim 1,
    상기 아민계 유기화합물은 화합물 분자 내 질소 원자를 1개 이상 포함하고, 탄소수 1 내지 5의 체인 길이를 갖는 알리파틱 구조의 탄화수소가 상기 질소 원자 1개당 1 내지 3의 결합을 갖는 화합물 중에서 선택된 1종 이상인 것인 표면외관이 우수한 전기아연도금강판용 아연 플래쉬 도금 용액.The amine-based organic compound includes at least one nitrogen atom in the compound molecule, and an hydrocarbon having an aliphatic structure having a chain length of 1 to 5 carbon atoms has one to three bonds per nitrogen atom. Zinc flash plating solution for electro-galvanized steel sheet excellent in the appearance of the above.
  4. 제 3항에 있어서,The method of claim 3, wherein
    상기 아민계 유기화합물은 상기 도금 용액 내에 0.05~10g/L로 포함하는 것인 표면외관이 우수한 전기아연도금강판용 아연 플래쉬 도금 용액.The amine-based organic compound is a zinc flash plating solution for electro-galvanized steel sheet excellent surface appearance that is contained in the plating solution at 0.05 ~ 10g / L.
  5. 제 1항에 있어서,The method of claim 1,
    상기 도금 용액은 1.0~5.0의 pH를 갖는 것인 표면외관이 우수한 전기아연도금강판용 아연 플래쉬 도금 용액.The plating solution is a zinc flash plating solution for electro-galvanized steel sheet excellent surface appearance that has a pH of 1.0 ~ 5.0.
  6. 소지강판을 탈지 및 산세 처리하는 단계;Degreasing and pickling the steel sheet;
    상기 소지강판을 아연 플래쉬 도금 용액을 이용하여 아연 플래쉬 도금을 행하는 단계; 및Performing zinc flash plating on the base steel sheet using a zinc flash plating solution; And
    상기 아연 플래쉬 도금된 소지강판을 전기아연도금처리하는 단계를 포함하고,Electro zinc-plating the zinc-plated base steel sheet, and
    상기 아연 플래쉬 도금 용액은 청구항 1 내지 5 중 어느 한 항의 도금 용액인 것인 표면외관이 우수한 전기아연도금강판의 제조방법.Wherein the zinc flash plating solution is a plating solution of any one of claims 1 to 5 excellent surface appearance of the manufacturing method of the electro-galvanized steel sheet.
  7. 제 6항에 있어서,The method of claim 6,
    상기 아연 플래쉬 도금은 용액 온도 상온~80℃, 전류밀도 1~100A/dm2, 아연 부착량 10~2000mg/m2으로 실시하는 것인 표면외관이 우수한 전기아연도금강판의 제조방법.The zinc flash plating is a method for producing an electro-zinc plated steel sheet having excellent surface appearance that is carried out at a solution temperature of room temperature ~ 80 ℃, current density of 1 ~ 100A / dm 2 , zinc adhesion amount 10 ~ 2000mg / m 2 .
  8. 제 6항에 있어서,The method of claim 6,
    상기 전기아연도금은 5~100g/m2의 아연 부착량으로 실시하는 것인 표면외관이 우수한 전기아연도금강판의 제조방법.The electro-zinc plating is a method for producing an electro-zinc plated steel sheet having excellent surface appearance that is carried out with a zinc adhesion amount of 5 ~ 100g / m 2 .
  9. 청구항 6의 방법에 의해 제조되고, 소지강판 및 상기 소지강판 상에 형성된 아연 플래쉬 도금층과 전기아연도금층을 순차적으로 포함하는 표면외관이 우수한 전기아연도금강판.An electrogalvanized steel sheet having excellent surface appearance, manufactured by the method of claim 6 and comprising a base steel sheet and a zinc flash plating layer formed on the base steel sheet and an electrogalvanized layer sequentially.
  10. 제 9항에 있어서,The method of claim 9,
    상기 소지강판은 냉연강판인 것인 표면외관이 우수한 전기아연도금강판.The base steel sheet is an electro-galvanized steel sheet having excellent surface appearance that is a cold rolled steel sheet.
PCT/KR2016/007790 2015-08-11 2016-07-18 Zinc flash plating solution for galvanized steel sheet having excellent surface appearance, method for manufacturing galvanized steel sheet using same, and galvanized steel sheet WO2017026683A1 (en)

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Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN116219510A (en) * 2022-12-30 2023-06-06 汉升五金塑胶制品(东莞)有限公司 High corrosion resistance electrogalvanized iron plate and production method thereof

Families Citing this family (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
KR102200134B1 (en) * 2018-09-28 2021-01-07 주식회사 포스코 High strength Electroplated Steel Sheet Having Excellent Hydrogen Crack Resistance
CN111270276A (en) * 2020-03-28 2020-06-12 武汉钢铁有限公司 Flash galvanizing plating solution and preparation method thereof and flash galvanizing method
CN111519221A (en) * 2020-04-15 2020-08-11 本钢板材股份有限公司 Processing method for single-side electrogalvanizing
JPWO2022186183A1 (en) * 2021-03-05 2022-09-09

Citations (5)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPH05247681A (en) * 1991-12-13 1993-09-24 Sollac Electrolytic bath for depositing and forming flash coating of iron-zinc alloy having high content of iron on substrate consisting of galvanealed steel
JPH06280088A (en) * 1993-03-25 1994-10-04 Nippon Steel Corp Galvanized aluminum and aluminum alloy excellent in adhesion property and production thereof
JPH0776792A (en) * 1993-09-07 1995-03-20 Nippon Steel Corp Production of electrogalvanized steel sheet excellent in surface appearance
KR20100121399A (en) * 2010-01-08 2010-11-17 주식회사 엠.이.시 Nickel flash plating solution, zinc-electroplated steel sheet and manufacturing method thereof
KR101288085B1 (en) * 2012-10-11 2013-08-07 남동화학(주) Zinc plated steel having iron flash plating film thereon and bath of iron flash plating and method for manufacturing the zinc plated steel

Family Cites Families (7)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS6379992A (en) * 1985-07-16 1988-04-09 Kawasaki Steel Corp Formation of electroplated zn-based film having superior paintability
JP3437663B2 (en) * 1995-01-17 2003-08-18 新日本製鐵株式会社 Manufacturing method of electro-galvanized steel sheet with excellent surface gloss
JP2001040494A (en) * 1999-07-27 2001-02-13 Kobe Steel Ltd Electrogalvanized steel sheet excellent in surface appearance and its production
JP4363708B2 (en) * 1999-08-05 2009-11-11 日本表面化学株式会社 Electrogalvanizing bath
FR2847275B1 (en) * 2002-11-19 2006-03-31 Usinor ZINC-BULK STEEL OR ZINC-LINED STEEL COATED WITH A ZINC OR ZINC ALLOY LAYER COMPRISING A POLYMER, AND METHOD OF MANUFACTURING BY ELECTRODEPOSITION
CN101660164B (en) * 2008-08-26 2011-12-28 宝山钢铁股份有限公司 Lubricating electro-galvanized steel plate and production method thereof
CN103911649B (en) * 2014-04-23 2016-08-17 桂林理工大学 A kind of preparation method of zinc bace composite coating layer

Patent Citations (5)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPH05247681A (en) * 1991-12-13 1993-09-24 Sollac Electrolytic bath for depositing and forming flash coating of iron-zinc alloy having high content of iron on substrate consisting of galvanealed steel
JPH06280088A (en) * 1993-03-25 1994-10-04 Nippon Steel Corp Galvanized aluminum and aluminum alloy excellent in adhesion property and production thereof
JPH0776792A (en) * 1993-09-07 1995-03-20 Nippon Steel Corp Production of electrogalvanized steel sheet excellent in surface appearance
KR20100121399A (en) * 2010-01-08 2010-11-17 주식회사 엠.이.시 Nickel flash plating solution, zinc-electroplated steel sheet and manufacturing method thereof
KR101288085B1 (en) * 2012-10-11 2013-08-07 남동화학(주) Zinc plated steel having iron flash plating film thereon and bath of iron flash plating and method for manufacturing the zinc plated steel

Cited By (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN116219510A (en) * 2022-12-30 2023-06-06 汉升五金塑胶制品(东莞)有限公司 High corrosion resistance electrogalvanized iron plate and production method thereof
CN116219510B (en) * 2022-12-30 2023-10-20 汉升五金塑胶制品(东莞)有限公司 High corrosion resistance electrogalvanized iron plate and production method thereof

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