CN110629144A - Channel steel hot galvanizing process - Google Patents
Channel steel hot galvanizing process Download PDFInfo
- Publication number
- CN110629144A CN110629144A CN201911048822.6A CN201911048822A CN110629144A CN 110629144 A CN110629144 A CN 110629144A CN 201911048822 A CN201911048822 A CN 201911048822A CN 110629144 A CN110629144 A CN 110629144A
- Authority
- CN
- China
- Prior art keywords
- channel steel
- acid
- galvanizing
- hot
- temperature
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Pending
Links
Classifications
-
- C—CHEMISTRY; METALLURGY
- C22—METALLURGY; FERROUS OR NON-FERROUS ALLOYS; TREATMENT OF ALLOYS OR NON-FERROUS METALS
- C22C—ALLOYS
- C22C38/00—Ferrous alloys, e.g. steel alloys
- C22C38/002—Ferrous alloys, e.g. steel alloys containing In, Mg, or other elements not provided for in one single group C22C38/001 - C22C38/60
-
- C—CHEMISTRY; METALLURGY
- C22—METALLURGY; FERROUS OR NON-FERROUS ALLOYS; TREATMENT OF ALLOYS OR NON-FERROUS METALS
- C22C—ALLOYS
- C22C38/00—Ferrous alloys, e.g. steel alloys
- C22C38/02—Ferrous alloys, e.g. steel alloys containing silicon
-
- C—CHEMISTRY; METALLURGY
- C22—METALLURGY; FERROUS OR NON-FERROUS ALLOYS; TREATMENT OF ALLOYS OR NON-FERROUS METALS
- C22C—ALLOYS
- C22C38/00—Ferrous alloys, e.g. steel alloys
- C22C38/04—Ferrous alloys, e.g. steel alloys containing manganese
-
- C—CHEMISTRY; METALLURGY
- C22—METALLURGY; FERROUS OR NON-FERROUS ALLOYS; TREATMENT OF ALLOYS OR NON-FERROUS METALS
- C22C—ALLOYS
- C22C38/00—Ferrous alloys, e.g. steel alloys
- C22C38/06—Ferrous alloys, e.g. steel alloys containing aluminium
-
- C—CHEMISTRY; METALLURGY
- C23—COATING METALLIC MATERIAL; COATING MATERIAL WITH METALLIC MATERIAL; CHEMICAL SURFACE TREATMENT; DIFFUSION TREATMENT OF METALLIC MATERIAL; COATING BY VACUUM EVAPORATION, BY SPUTTERING, BY ION IMPLANTATION OR BY CHEMICAL VAPOUR DEPOSITION, IN GENERAL; INHIBITING CORROSION OF METALLIC MATERIAL OR INCRUSTATION IN GENERAL
- C23C—COATING METALLIC MATERIAL; COATING MATERIAL WITH METALLIC MATERIAL; SURFACE TREATMENT OF METALLIC MATERIAL BY DIFFUSION INTO THE SURFACE, BY CHEMICAL CONVERSION OR SUBSTITUTION; COATING BY VACUUM EVAPORATION, BY SPUTTERING, BY ION IMPLANTATION OR BY CHEMICAL VAPOUR DEPOSITION, IN GENERAL
- C23C2/00—Hot-dipping or immersion processes for applying the coating material in the molten state without affecting the shape; Apparatus therefor
- C23C2/02—Pretreatment of the material to be coated, e.g. for coating on selected surface areas
-
- C—CHEMISTRY; METALLURGY
- C23—COATING METALLIC MATERIAL; COATING MATERIAL WITH METALLIC MATERIAL; CHEMICAL SURFACE TREATMENT; DIFFUSION TREATMENT OF METALLIC MATERIAL; COATING BY VACUUM EVAPORATION, BY SPUTTERING, BY ION IMPLANTATION OR BY CHEMICAL VAPOUR DEPOSITION, IN GENERAL; INHIBITING CORROSION OF METALLIC MATERIAL OR INCRUSTATION IN GENERAL
- C23C—COATING METALLIC MATERIAL; COATING MATERIAL WITH METALLIC MATERIAL; SURFACE TREATMENT OF METALLIC MATERIAL BY DIFFUSION INTO THE SURFACE, BY CHEMICAL CONVERSION OR SUBSTITUTION; COATING BY VACUUM EVAPORATION, BY SPUTTERING, BY ION IMPLANTATION OR BY CHEMICAL VAPOUR DEPOSITION, IN GENERAL
- C23C2/00—Hot-dipping or immersion processes for applying the coating material in the molten state without affecting the shape; Apparatus therefor
- C23C2/04—Hot-dipping or immersion processes for applying the coating material in the molten state without affecting the shape; Apparatus therefor characterised by the coating material
- C23C2/06—Zinc or cadmium or alloys based thereon
-
- C—CHEMISTRY; METALLURGY
- C23—COATING METALLIC MATERIAL; COATING MATERIAL WITH METALLIC MATERIAL; CHEMICAL SURFACE TREATMENT; DIFFUSION TREATMENT OF METALLIC MATERIAL; COATING BY VACUUM EVAPORATION, BY SPUTTERING, BY ION IMPLANTATION OR BY CHEMICAL VAPOUR DEPOSITION, IN GENERAL; INHIBITING CORROSION OF METALLIC MATERIAL OR INCRUSTATION IN GENERAL
- C23C—COATING METALLIC MATERIAL; COATING MATERIAL WITH METALLIC MATERIAL; SURFACE TREATMENT OF METALLIC MATERIAL BY DIFFUSION INTO THE SURFACE, BY CHEMICAL CONVERSION OR SUBSTITUTION; COATING BY VACUUM EVAPORATION, BY SPUTTERING, BY ION IMPLANTATION OR BY CHEMICAL VAPOUR DEPOSITION, IN GENERAL
- C23C2/00—Hot-dipping or immersion processes for applying the coating material in the molten state without affecting the shape; Apparatus therefor
- C23C2/26—After-treatment
-
- C—CHEMISTRY; METALLURGY
- C23—COATING METALLIC MATERIAL; COATING MATERIAL WITH METALLIC MATERIAL; CHEMICAL SURFACE TREATMENT; DIFFUSION TREATMENT OF METALLIC MATERIAL; COATING BY VACUUM EVAPORATION, BY SPUTTERING, BY ION IMPLANTATION OR BY CHEMICAL VAPOUR DEPOSITION, IN GENERAL; INHIBITING CORROSION OF METALLIC MATERIAL OR INCRUSTATION IN GENERAL
- C23C—COATING METALLIC MATERIAL; COATING MATERIAL WITH METALLIC MATERIAL; SURFACE TREATMENT OF METALLIC MATERIAL BY DIFFUSION INTO THE SURFACE, BY CHEMICAL CONVERSION OR SUBSTITUTION; COATING BY VACUUM EVAPORATION, BY SPUTTERING, BY ION IMPLANTATION OR BY CHEMICAL VAPOUR DEPOSITION, IN GENERAL
- C23C22/00—Chemical surface treatment of metallic material by reaction of the surface with a reactive liquid, leaving reaction products of surface material in the coating, e.g. conversion coatings, passivation of metals
- C23C22/05—Chemical surface treatment of metallic material by reaction of the surface with a reactive liquid, leaving reaction products of surface material in the coating, e.g. conversion coatings, passivation of metals using aqueous solutions
- C23C22/06—Chemical surface treatment of metallic material by reaction of the surface with a reactive liquid, leaving reaction products of surface material in the coating, e.g. conversion coatings, passivation of metals using aqueous solutions using aqueous acidic solutions with pH less than 6
- C23C22/07—Chemical surface treatment of metallic material by reaction of the surface with a reactive liquid, leaving reaction products of surface material in the coating, e.g. conversion coatings, passivation of metals using aqueous solutions using aqueous acidic solutions with pH less than 6 containing phosphates
Landscapes
- Chemical & Material Sciences (AREA)
- Engineering & Computer Science (AREA)
- Materials Engineering (AREA)
- Mechanical Engineering (AREA)
- Metallurgy (AREA)
- Organic Chemistry (AREA)
- Chemical Kinetics & Catalysis (AREA)
- General Chemical & Material Sciences (AREA)
- Coating With Molten Metal (AREA)
- Other Surface Treatments For Metallic Materials (AREA)
Abstract
The invention relates to a hot galvanizing process for channel steel, which comprises the following steps: s1, preprocessing, namely degreasing the channel steel to be processed until the channel steel is soaked in water; s2, carrying out acid washing on the channel steel; s3, preheating: s4, hot galvanizing: s5, passivation: s6, cooling: and S7, checking and packaging. By adopting the galvanizing process, the galvanized channel steel can form a compact composite film, and the corrosion resistance of a hot-dip galvanizing passivation layer can be obviously improved.
Description
Technical Field
The invention relates to the technical field of hot galvanizing channel steel, in particular to a hot galvanizing process for channel steel.
Background
The prior galvanized steel channel has complex galvanizing process in the galvanizing treatment process, secondly, the galvanized steel channel is passivated by most chromates, hexavalent chromium has high toxicity and carcinogenicity in the chromating process and is gradually eliminated by the market, and the prior market adopts chromium-free passivation solution, titanium salt passivation solution, phosphate pseudo-conversion passivation solution and the like, but the corrosion resistance of the zinc-plated steel channel cannot completely meet the practical application requirements.
Secondly, in the current hot dip galvanized steel channel, the adhesion between a zinc coating and the steel channel is low, and the problems of coating pulverization and peeling exist in the processes of steel channel, transportation and welding, and a method for controlling the adhesion between the coating and the steel channel by changing the components of the steel channel or the components of the zinc coating does not exist at present.
Disclosure of Invention
The technical problem to be solved by the invention is as follows: overcomes the defects of the prior art, provides a hot galvanizing process for channel steel, and solves the problems of relatively complex galvanizing process and poor corrosion resistance in the prior art.
The technical scheme adopted by the invention for solving the technical problems is as follows: a hot galvanizing process for channel steel comprises the following steps:
s1, preprocessing, namely degreasing the channel steel to be processed until the channel steel is soaked in water;
s2, carrying out acid washing on the channel steel;
s3, preheating: drying and preheating the pickled channel steel at the preheating temperature of 90-120 ℃;
s4: hot galvanizing: conveying the channel steel to a galvanizing pot for hot galvanizing;
s5, passivation: passivating by using a passivation solution;
s6, cooling: cooling the channel steel by adopting a water cooling mode, wherein the cooling temperature is 50-70 ℃;
and S7, checking and packaging.
Further, the acid washing in the step 2 comprises rough acid washing, high-pressure water washing, fine acid washing, water washing, antirust liquid soaking, high-pressure antirust liquid washing, blow-drying and inner cavity cleaning;
the temperature of the acid liquor is 25-45 ℃ during rough pickling, and a sponge projectile is adopted to clean the inner cavity of the pipeline.
Further, in the step S5, the passivation solution is composed of 1.2 to 1.8 wt% of aminotrimethylene phosphonic acid, 3.2 to 5.8 wt% of phosphate, 12.0 to 15.0 wt% of silicone modified epoxy resin, 0.3 to 0.5 wt% of boric acid, 2.3 to 2.8 wt% of organic acid and water, and the organic acid is one or more organic acids selected from citric acid, tartaric acid, malic acid, salicylic acid or lactic acid.
Further, the organic silicon modified epoxy resin is prepared by the following method: putting epoxy resin E-20 and a butyl titanate catalyst into a three-neck flask provided with a stirrer, a reflux condenser tube and a dropping funnel, heating to 100-120 ℃, and then starting stirring, wherein the mass ratio of the epoxy resin E-20 to the butyl titanate catalyst is 10: 0.1-0.2; then, the following steps of Z6018 organic silicon: slowly dropwise adding a xylene solution of Z6018 organosilicon according to the mass ratio of 1: 2 of E-20, reacting at 200 ℃ for 4.5-5.5 hours, refluxing, condensing, and continuously separating out small molecular compound alcohol and water generated by the reaction to obtain the organosilicon modified epoxy resin.
Further, in step S4, in the hot dip galvanizing operation, the temperature of the steel sheet is 455-465 ℃ when the steel sheet is put into the plating bath, the temperature of the plating bath in the zinc pot is 450-460 ℃, the Fe content in the plating bath is less than 0.03%, and the Al content in the plating bath is: 0.21-0.25%, unit speed: 100-110 m/min, the cooling rate of the steel plate is 0%, and the high span temperature is as follows: 235 to 245 ℃.
Further, the channel steel comprises, by weight: 0.03 to 0.07%, Mn: 0.01 to 0.03%, Si: 0.19-0.30%, P: 0.006-0.019%, S: 0.009-0.020%, Al: 0.02-0.07%, and the balance of Fe.
The invention has the beneficial effects that:
the hot galvanizing process is simple, a plurality of repetitive processes are omitted, the working efficiency is improved, and the galvanizing effect is good.
By adopting the galvanizing process, the galvanized channel steel can form a compact composite film, and the corrosion resistance of a hot-dip galvanizing passivation layer can be obviously improved.
By adopting the galvanizing process, the Fe-Al intermediate transition layer between the channel steel and the zinc coating can prevent mutual diffusion between Fe and Zn, the formation of an Fe-Zn alloy layer is reduced, a gamma phase cannot be formed in the coating, the delta phase is relatively thin, the xi phase is less, most of the coating consists of the eta phase, the adhesiveness of the coating of the hot-dip galvanized steel plate is improved, and the phenomena of zinc powder falling, stripping and the like of the coating are reduced;
the grain orientation of the coating of the hot-dip galvanized steel channel is optimized, and the scratch resistance, the wear resistance and the adhesion performance of the coating are obviously improved.
Detailed Description
The invention will now be further described with reference to specific examples.
A hot galvanizing process for channel steel comprises the following steps:
s1, preprocessing, namely degreasing the channel steel to be processed until the channel steel is soaked in water;
s2, carrying out acid washing on the channel steel;
s3, preheating: drying and preheating the pickled channel steel at the preheating temperature of 90-120 ℃;
s4: hot galvanizing: conveying the channel steel to a galvanizing pot for hot galvanizing;
s5, passivation: passivating by using a passivation solution;
s6, cooling: cooling the channel steel by adopting a water cooling mode, wherein the cooling temperature is 50-70 ℃;
and S7, checking and packaging.
Specifically, the acid washing in the step 2 comprises rough acid washing, high-pressure water washing, fine acid washing, water washing, antirust liquid soaking, high-pressure antirust liquid washing, blow-drying and inner cavity cleaning; the temperature of the acid liquor is 25-45 ℃ during rough pickling, and a sponge projectile is adopted to clean the inner cavity of the pipeline.
Specifically, in step S5, the passivation solution includes 1.2 to 1.8 wt% of aminotrimethylene phosphonic acid, 3.2 to 5.8 wt% of phosphate, 12.0 to 15.0 wt% of silicone modified epoxy resin, 0.3 to 0.5 wt% of boric acid, 2.3 to 2.8 wt% of organic acid and water, and the organic acid is one or more organic acids selected from citric acid, tartaric acid, malic acid, salicylic acid and lactic acid.
Specifically, the organic silicon modified epoxy resin is prepared by the following method: putting epoxy resin E-20 and a butyl titanate catalyst into a three-neck flask provided with a stirrer, a reflux condenser tube and a dropping funnel, heating to 100-120 ℃, and then starting stirring, wherein the mass ratio of the epoxy resin E-20 to the butyl titanate catalyst is 10: 0.1-0.2; then, the following steps of Z6018 organic silicon: slowly dropwise adding a xylene solution of Z6018 organosilicon according to the mass ratio of 1: 2 of E-20, reacting at 200 ℃ for 4.5-5.5 hours, refluxing, condensing, and continuously separating out small molecular compound alcohol and water generated by the reaction to obtain the organosilicon modified epoxy resin.
Specifically, in step S4, in the hot dip galvanizing operation, the temperature of the steel sheet is 455-465 ℃ when the steel sheet is put into the plating bath, the temperature of the plating bath in the zinc pot is 450-460 ℃, the Fe content in the plating bath is less than 0.03%, and the Al content in the plating bath is: 0.21-0.25%, unit speed: 100-110 m/min, the cooling rate of the steel plate is 0%, and the high span temperature is as follows: 235 to 245 ℃.
Specifically, the channel steel comprises, by weight: 0.03 to 0.07%, Mn: 0.01 to 0.03%, Si: 0.19-0.30%, P: 0.006-0.019%, S: 0.009-0.020%, Al: 0.02-0.07%, and the balance of Fe.
The hot galvanizing process is simple, a plurality of repetitive processes are omitted, the working efficiency is improved, and the galvanizing effect is good.
Secondly, the surface of the hot-dip galvanized channel steel passivated by zirconium salt, titanium salt or phosphate is easy to form the phenomenon of zinc corrosion in the actual use process, namely the phenomenon of white powder in general; once the situation occurs, the corrosion resistance of the zinc coating is greatly reduced, and the main reason for the situation is that the compactness of the passive film in the prior art is poor, so that water, carbon dioxide and other acids in the air can form electrolyte on the surface of the zinc tube in an alkaline environment, so that zinc on the surface of the zinc tube is formed by a microcell reaction, the zinc corrosion is accelerated, and the service life of the hot galvanized channel steel is seriously shortened. By adopting the passivation process, a compact composite film can be formed, and the corrosion resistance of the passivation layer can be obviously improved.
By adopting the galvanizing process, the Fe-Al intermediate transition layer between the channel steel and the zinc coating can prevent mutual diffusion between Fe and Zn, the formation of an Fe-Zn alloy layer is reduced, a gamma phase cannot be formed in the coating, the delta phase is relatively thin, the xi phase is less, most of the coating consists of the eta phase, the adhesiveness of the coating of the hot-dip galvanized steel plate is improved, and the phenomena of zinc powder falling, stripping and the like of the coating are reduced; the grain orientation of the coating of the hot-dip galvanized steel channel is optimized, and the scratch resistance, the wear resistance and the adhesion performance of the coating are obviously improved.
In light of the foregoing description of the preferred embodiment of the present invention, many modifications and variations will be apparent to those skilled in the art without departing from the spirit and scope of the invention. The technical scope of the present invention is not limited to the content of the specification, and must be determined according to the scope of the claims.
Claims (6)
1. A channel steel hot galvanizing technology is characterized by comprising the following steps:
s1, preprocessing, namely degreasing the channel steel to be processed until the channel steel is soaked in water;
s2, carrying out acid washing on the channel steel;
s3, preheating: drying and preheating the pickled channel steel at the preheating temperature of 90-120 ℃;
s4: hot galvanizing: conveying the channel steel to a galvanizing pot for hot galvanizing;
s5, passivation: passivating by using a passivation solution;
s6, cooling: cooling the channel steel by adopting a water cooling mode, wherein the cooling temperature is 50-70 ℃;
and S7, checking and packaging.
2. A hot galvanizing process for channel steel according to claim 1, wherein the pickling in the step 2 comprises rough pickling, high-pressure water washing, fine pickling, water washing, antirust liquid soaking, high-pressure antirust liquid cleaning, blow drying and cavity cleaning;
the temperature of the acid liquor is 25-45 ℃ during rough pickling, and a sponge projectile is adopted to clean the inner cavity of the pipeline.
3. The process of hot galvanizing channel steel as claimed in claim 1, wherein in the step S5, the passivation solution includes aminotrimethylene phosphonic acid 1.2 to 1.8 wt%, phosphate 3.2 to 5.8 wt%, silicone modified epoxy resin 12.0 to 15.0 wt%, boric acid 0.3 to 0.5 wt%, organic acid 2.3 to 2.8 wt%, and water, and the organic acid is one or more selected from citric acid, tartaric acid, malic acid, salicylic acid, and lactic acid.
4. The channel steel hot galvanizing process of claim 3, wherein the organosilicon modified epoxy resin is prepared by the following method: putting epoxy resin E-20 and a butyl titanate catalyst into a three-neck flask provided with a stirrer, a reflux condenser tube and a dropping funnel, heating to 100-120 ℃, and then starting stirring, wherein the mass ratio of the epoxy resin E-20 to the butyl titanate catalyst is 10: 0.1-0.2; then, the following steps of Z6018 organic silicon: slowly dropwise adding a xylene solution of Z6018 organosilicon according to the mass ratio of 1: 2 of E-20, reacting at 200 ℃ for 4.5-5.5 hours, refluxing, condensing, and continuously separating out small molecular compound alcohol and water generated by the reaction to obtain the organosilicon modified epoxy resin.
5. A hot dip galvanizing process for U-steel according to claim 3, wherein in step S4, the temperature of the steel sheet in the plating bath during the hot dip galvanizing operation is 455-465 ℃, the temperature of the plating bath in the zinc pot is 450-460 ℃, the Fe content in the plating bath is less than 0.03%, and the Al content in the plating bath is as follows: 0.21-0.25%, unit speed: 100-110 m/min, the cooling rate of the steel plate is 0%, and the high span temperature is as follows: 235 to 245 ℃.
6. A process for galvanizing a channel steel according to claim 1, wherein the channel steel comprises, in weight percent, C: 0.03 to 0.07%, Mn: 0.01 to 0.03%, Si: 0.19-0.30%, P: 0.006-0.019%, S: 0.009-0.020%, Al: 0.02-0.07%, and the balance of Fe.
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
CN201911048822.6A CN110629144A (en) | 2019-10-31 | 2019-10-31 | Channel steel hot galvanizing process |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
CN201911048822.6A CN110629144A (en) | 2019-10-31 | 2019-10-31 | Channel steel hot galvanizing process |
Publications (1)
Publication Number | Publication Date |
---|---|
CN110629144A true CN110629144A (en) | 2019-12-31 |
Family
ID=68978284
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
CN201911048822.6A Pending CN110629144A (en) | 2019-10-31 | 2019-10-31 | Channel steel hot galvanizing process |
Country Status (1)
Country | Link |
---|---|
CN (1) | CN110629144A (en) |
Citations (6)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US4814210A (en) * | 1984-11-09 | 1989-03-21 | Werner Ackermann | Process and means for hot-dip galvanizing finned tubes |
CN1544701A (en) * | 2003-11-21 | 2004-11-10 | 三一重工股份有限公司 | Steel pipe acid pickling process |
CN101323941A (en) * | 2008-07-31 | 2008-12-17 | 攀钢集团研究院有限公司 | Galvanizing method of hot dip galvanizing steel plate |
CN102776458A (en) * | 2012-07-09 | 2012-11-14 | 天津市宝利金制管有限公司 | Single-side galvanizing method for producing hot-dip galvanized steel pipe |
CN103924235A (en) * | 2014-04-22 | 2014-07-16 | 刘建忠 | Passivation process of hot dip galvanized steel plate |
CN105648379A (en) * | 2014-12-03 | 2016-06-08 | 重庆业高家具有限公司 | Hot-dip galvanizing technology |
-
2019
- 2019-10-31 CN CN201911048822.6A patent/CN110629144A/en active Pending
Patent Citations (6)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US4814210A (en) * | 1984-11-09 | 1989-03-21 | Werner Ackermann | Process and means for hot-dip galvanizing finned tubes |
CN1544701A (en) * | 2003-11-21 | 2004-11-10 | 三一重工股份有限公司 | Steel pipe acid pickling process |
CN101323941A (en) * | 2008-07-31 | 2008-12-17 | 攀钢集团研究院有限公司 | Galvanizing method of hot dip galvanizing steel plate |
CN102776458A (en) * | 2012-07-09 | 2012-11-14 | 天津市宝利金制管有限公司 | Single-side galvanizing method for producing hot-dip galvanized steel pipe |
CN103924235A (en) * | 2014-04-22 | 2014-07-16 | 刘建忠 | Passivation process of hot dip galvanized steel plate |
CN105648379A (en) * | 2014-12-03 | 2016-06-08 | 重庆业高家具有限公司 | Hot-dip galvanizing technology |
Similar Documents
Publication | Publication Date | Title |
---|---|---|
CN101454474B (en) | Process for producing a sheet steel product coated with an anticorrosion system | |
CN111270182A (en) | Hot-dip Zn-Al-Mg alloy coated steel plate and preparation method thereof | |
CN111304573A (en) | Zinc-aluminum-magnesium alloy coated steel plate with excellent corrosion resistance and preparation method thereof | |
JP4757608B2 (en) | Zn-based alloy plated steel | |
JP2000064061A (en) | Precoated steel sheet excellent in corrosion resistance | |
JP2000104154A (en) | Plated steel sheet and coated steel sheet excellent in corrosion resistance and production of the same | |
JP3476408B2 (en) | Hot-dip Zn-Mg-Al alloy-plated steel wire and method for producing the same | |
CN110257747B (en) | Ultrathin coating hot-dip galvanized steel plate and manufacturing process thereof | |
CN102776458A (en) | Single-side galvanizing method for producing hot-dip galvanized steel pipe | |
CN109852914A (en) | A kind of high-strength alloyed steel plate hot dip galvanizing process | |
CN110499485B (en) | Alloying treatment method for preparing high-pulverization-resistance hot-dip galvanized coating | |
EP0755419A1 (en) | Polymer composition and method for treating metal surfaces | |
JP4537599B2 (en) | High corrosion resistance Al-based plated steel sheet with excellent appearance | |
CN110629144A (en) | Channel steel hot galvanizing process | |
CN111575622A (en) | Aluminum-plated steel sheet for hot-formed parts having excellent coating properties, method for producing same, and hot-formed parts | |
WO2023098125A1 (en) | Zinc-aluminum-magnesium alloy coated steel containing v and b and preparation method therefor | |
CN1114665C (en) | Zinc base water soluble anti-corrosion paint for metal surface and its prepn. method | |
CN110205522B (en) | Zinc-aluminum-chromium-calcium-silicon alloy for hot dipping and hot galvanizing method | |
CN110117758B (en) | Low-temperature impact resistant instrument shell part and preparation method thereof | |
JP2968147B2 (en) | Acid displacement plating solution composition for zinc-containing metal plated steel sheet | |
CN111719072A (en) | Zn-Al-Si-Mn-Bi-Ti-Ce alloy for hot dip coating and use method thereof | |
CN106811708A (en) | The galvanized method of steel plate | |
CN112575273A (en) | Medium-aluminum zinc-aluminum-magnesium coated steel plate with excellent coating plasticity and production method thereof | |
CN110241369B (en) | Zinc-aluminum-nickel-tantalum alloy for hot dipping and hot galvanizing method | |
CN103924228A (en) | Metal material with excellent corrosion resistance |
Legal Events
Date | Code | Title | Description |
---|---|---|---|
PB01 | Publication | ||
PB01 | Publication | ||
SE01 | Entry into force of request for substantive examination | ||
SE01 | Entry into force of request for substantive examination | ||
RJ01 | Rejection of invention patent application after publication |
Application publication date: 20191231 |
|
RJ01 | Rejection of invention patent application after publication |