JP3811109B2 - Hot-dip zinc-aluminum alloy plating method - Google Patents

Hot-dip zinc-aluminum alloy plating method Download PDF

Info

Publication number
JP3811109B2
JP3811109B2 JP2002243391A JP2002243391A JP3811109B2 JP 3811109 B2 JP3811109 B2 JP 3811109B2 JP 2002243391 A JP2002243391 A JP 2002243391A JP 2002243391 A JP2002243391 A JP 2002243391A JP 3811109 B2 JP3811109 B2 JP 3811109B2
Authority
JP
Japan
Prior art keywords
zinc
aluminum alloy
plating
molten
aluminum
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.)
Expired - Fee Related
Application number
JP2002243391A
Other languages
Japanese (ja)
Other versions
JP2004083950A (en
Inventor
洋 小川
和隆 中島
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
Dowa Holdings Co Ltd
Original Assignee
Dowa Holdings Co Ltd
Dowa Mining Co Ltd
Priority date (The priority date 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 date listed.)
Filing date
Publication date
Application filed by Dowa Holdings Co Ltd, Dowa Mining Co Ltd filed Critical Dowa Holdings Co Ltd
Priority to JP2002243391A priority Critical patent/JP3811109B2/en
Publication of JP2004083950A publication Critical patent/JP2004083950A/en
Application granted granted Critical
Publication of JP3811109B2 publication Critical patent/JP3811109B2/en
Anticipated expiration legal-status Critical
Expired - Fee Related legal-status Critical Current

Links

Description

【0001】
【発明の属する技術分野】
本発明は、鋼材の表面に亜鉛−アルミニウム合金めっきを施す溶融亜鉛−アルミニウム合金めっき方法に関する。
【0002】
【従来の技術】
従来、建材、自動車部品、一般構造部材などに使用される鉄鋼材料の腐食を防止するために、鋼材に溶融亜鉛めっきや溶融亜鉛−アルミニウム合金めっきが施されている。特に、ここ数年、環境悪化の影響を防ぐために、より高い耐食性の溶融亜鉛−アルミニウム合金めっきの需要が高まってきており、溶融亜鉛−アルミニウム合金めっきを施すことが要求される製品も多岐に渡っている。
【0003】
このような溶融亜鉛−アルミニウム合金めっきの一般的な方法として、特許第2924894号公報に開示された2浴法といわれる方法がある。この2浴法は、鋼材を亜鉛浴に浸漬させて亜鉛めっきした後に、この亜鉛めっきした鋼材を再度亜鉛−アルミニウム合金浴に浸漬させてめっきを行う方法である。また、他の方法として、鋼材のめっき工程の前処理段階において、溶融塩をフラックスとして使用して、1回の浸漬により鋼材の溶融亜鉛−アルミニウム合金めっきを行う方法も実用化されている。
【0004】
【発明が解決しようとする課題】
しかし、溶融亜鉛−アルミニウム合金めっきの2溶法では、2つのめっき槽が必要になり、設備的に大掛かりになるという問題がある。また、10mクラスの大型構造物に亜鉛−アルミニウム合金めっきを行うのは非常に難しく、仕上がり品質を考慮すると、このようなめっきを行うことは不可能に近い。10mクラスの大型構造物に対応するめっき槽が無く、大型構造物の場合におけるめっき条件(めっき温度、浸漬時間)の設定が困難であり、不めっき(めっきが付かないこと)に対応することができない(亜鉛めっきの場合は不めっきの発生時に再浸漬してめっきを付けているが、亜鉛−アルミニウム合金の場合は再浸漬してもめっきが付かないし、表面状態が悪くなる)からである。
【0005】
一方、溶融塩フラックスを使用する方法では、めっき面に付着した溶融塩フラックスを酸洗して除去する工程が必要になり、そのための洗浄槽が必要になるため、10mクラスの大型構造物に対応するにはそれ相応の設備投資が必要になり、工程の増加による効率の低下とコストアップが問題となる。
【0006】
また、鋼材に施された溶融亜鉛めっき層は、亜鉛と鉄の合金化反応によりめっき層と鉄素地との間に亜鉛−鉄合金層を形成することによって強固になり、更に、亜鉛−アルミニウム合金溶湯と反応することにより、アルミニウム−鉄合金層および亜鉛−アルミニウム−鉄合金層が形成される。そのため、溶融亜鉛めっき層と亜鉛−アルミニウム合金溶湯との反応をどのような方法で行うかが問題となるが、上述したように鋼材を亜鉛−アルミニウム合金溶湯に浸漬させる方法は困難であるので、他の方法が求められる。
【0007】
したがって、本発明は、このような従来の問題点に鑑み、工程の増加による効率の低下とコストアップを防止でき、大型の鋼材にも簡易且つ確実に亜鉛−アルミニウム合金めっきを施すことができる溶融亜鉛−アルミニウム合金めっき方法を提供することを目的とする。
【0008】
【課題を解決するための手段】
本発明者らは、上記課題を解決するために鋭意研究した結果、鋼材の表面に予め亜鉛めっきを施し、このめっき面を加熱してめっき面が反応可能な温度にした後、表面に亜鉛−アルミニウム合金溶湯を注ぎかけることにより、表面の凹凸、やけなどがない耐食性の高いアルミニウム−鉄合金層および亜鉛−アルミニウム−鉄合金層が形成されることを見出し、本発明を完成するに至った。
【0009】
すなわち、本発明による溶融亜鉛−アルミニウム合金めっき方法は、鋼材の表面に亜鉛めっきを施し、このめっきを凝固させた後、このめっき層が溶融状態になり得る温度(420℃)以上に加熱して保持亜鉛めっきが施された鋼材の表面に亜鉛−アルミニウム合金溶湯を注ぎかけることを特徴とする。
【0010】
この溶融亜鉛−アルミニウム合金めっき方法において、溶融亜鉛−アルミニウム溶湯が、1〜60wt%のアルミニウムを含み、残部として亜鉛を含むのが好ましい。さらに、溶融亜鉛−アルミニウム溶湯が、Mg、Si、NiおよびBiから選ばれた少なくとも1種以上を0.1〜3wt%含むのが好ましい。また、溶融亜鉛−アルミニウム溶湯の温度が420〜650℃であるのが好ましい。
【0011】
【発明の実施の形態】
本発明による溶融亜鉛−アルミニウム合金めっき方法の実施の形態では、鋼材の表面に亜鉛めっきを施し、このめっきを凝固させた後、めっき表面の亜鉛層が溶融状態になり得る温度(420℃)以上に加熱して保持亜鉛めっきが施された鋼材の表面に420〜650℃の亜鉛−アルミニウム合金溶湯を注ぎかけることにより、鋼材に溶融亜鉛−アルミニウム合金めっきを施す。
【0012】
鋼管の外面に溶融亜鉛めっきを施す方法として鋼材面に亜鉛溶湯を注ぎかける方法は既に提案されているが、本発明による溶融亜鉛−アルミニウム合金めっき方法の実施の形態では、従来難しいとされてきた大型構造物や大型鋼管の溶融亜鉛−アルミニウム合金めっきを連続的に行うことが可能となる。
【0013】
また、従来の被めっき物を亜鉛−アルミニウム合金溶湯に浸漬させる方法では、めっき槽の大きさにより被めっき物の大きさが制限されるが、本発明による溶融亜鉛−アルミニウム合金めっき方法の実施の形態のように亜鉛−アルミニウム合金溶湯を注ぎかける方法であれば、めっき槽の大きさに左右されること無く連続的にめっきを施すことが可能となる。
【0014】
本発明による溶融亜鉛−アルミニウム合金めっき方法の実施の形態では、脱脂、酸洗、フラックス処理、亜鉛めっきなどの通常の溶融亜鉛めっき工程の後に、予熱を行い、亜鉛−アルミニウム合金溶湯を注ぐ工程を経て、ワイピングを行い、冷却することにより、最終的な製品とする。
【0015】
本発明による溶融亜鉛−アルミニウム合金めっき方法の実施の形態において、溶融亜鉛−アルミニウム溶湯が、1〜60wt%のアルミニウムを含み、残部として亜鉛を含むのが好ましい。アルミニウム濃度を1〜60wt%とする理由は、60wt%を超えると、得られる耐食性に変わりは無いが、濃度が高くなることにより合金の融点が上昇して作業性が悪くなり、一方、1wt%を下回ると耐食性を維持する効果が薄れてくるからである。
【0016】
さらに、溶融亜鉛−アルミニウム溶湯が、Mg、Si、NiおよびBiから選ばれた少なくとも1種以上を0.1〜3wt%含むのが好ましい。Mg、Si、Ni、Biを添加する理由は、加工性、密着性、湯流れ性などが向上するからであり、これらの濃度を0.1〜3wt%にする理由は、0.1wt%を下回ると、そのような効果が薄くなり、一方、3wt%を超えると、加工性が低下して品質に悪影響を及ぼす(曲げ加工時に割れが発生する場合があり、また、たれの発生も考えられる)からである。
【0017】
【実施例】
以下、本発明による溶融亜鉛−アルミニウム合金めっき方法の実施例について詳細に説明する。
【0018】
[実施例1]
試験片として、一般構造物材料のSS材のプレート(100×70×3.2mm)を用意した。この試験片を70℃のNaOH水溶液に10分間浸漬して脱脂を行い、水洗後、HC1溶液に60分間浸漬して酸洗し、水洗後、70℃のフラックス液に1分間浸漬し、乾燥後、440〜470℃の亜鉛浴に5〜10分間浸漬して、亜鉛めっきを行った。なお、亜鉛浴として電気亜鉛地金を溶解した浴を使用した。
【0019】
このようにして亜鉛めっきしたプレートを電気ヒーター内に宙吊りにし、表面温度が430℃(めっき表面の亜鉛層が溶融状態になり得る温度(420℃)以上)になるまで加熱した。
【0020】
次いで、電気ヒーターから取出したプレートに5wt%のAlと残部が亜鉛からなる420〜450℃の亜鉛−アルミニウム合金溶湯を注ぎかけた(接触時間は約10秒)。なお、亜鉛−アルミニウム合金溶湯に用いる亜鉛として電気亜鉛地金を使用した。
【0021】
このようにして亜鉛−アルミニウム合金めっきを施したプレートのめっき状態について観察したところ、表面の凹凸、やけ(被めっき鋼材中の不純物の影響やめっき温度が高すぎることなどにより、めっき層中のZn−Fe合金層が異常成長してめっき面が灰色に変色すること)、不めっき、たれのいずれも無く、めっき状態は良好であった。
【0022】
[実施例2]
30wt%のAlと残部が亜鉛からなる530〜570℃の亜鉛−アルミニウム合金溶湯を注いだ以外は、実施例1と同様の方法により、亜鉛−アルミニウム合金めっきを行ったところ、表面の凹凸、やけ、不めっき、たれのいずれも無く、めっき状態は良好であった。
【0023】
[実施例3]
55wt%のAlと1.6wt%のSiと残部が亜鉛からなる610〜650℃の亜鉛−アルミニウム合金溶湯を注いだ以外は、実施例1と同様の方法により、亜鉛−アルミニウム合金めっきを行ったところ、表面の凹凸、やけ、不めっき、たれのいずれも無く、めっき状態は良好であった。
【0024】
[実施例4]
5wt%のAlと1wt%のMgと残部が亜鉛からなる亜鉛−アルミニウム合金溶湯を注いだ以外は、実施例1と同様の方法により、亜鉛−アルミニウム合金めっきを行ったところ、表面の凹凸、やけ、不めっき、たれのいずれも無く、めっき状態は良好であった。
【0025】
[実施例5]
5wt%のAlと1wt%のNiと残部が亜鉛からなる亜鉛−アルミニウム合金溶湯を注いだ以外は、実施例1と同様の方法により、亜鉛−アルミニウム合金めっきを行ったところ、表面の凹凸、やけ、不めっき、たれのいずれも無く、めっき状態は良好であった。
【0026】
[実施例6]
5wt%のAlと1wt%のBiと残部が亜鉛からなる亜鉛−アルミニウム合金溶湯を注いだ以外は、実施例1と同様の方法により、亜鉛−アルミニウム合金めっきを行ったところ、表面の凹凸、やけ、不めっき、たれのいずれも無く、めっき状態は良好であった。
【0027】
【発明の効果】
上述したように、本発明の溶融亜鉛−アルミニウム合金めっき方法によれば、工程の増加による効率の低下とコストアップを防止でき、大型の鋼材にも簡易且つ確実に亜鉛−アルミニウム合金めっきを施すことができる。
[0001]
BACKGROUND OF THE INVENTION
The present invention relates to a hot dip zinc-aluminum alloy plating method for performing zinc-aluminum alloy plating on the surface of a steel material.
[0002]
[Prior art]
Conventionally, in order to prevent corrosion of steel materials used for building materials, automobile parts, general structural members, etc., hot dip galvanization and hot dip zinc-aluminum alloy plating have been applied to steel materials. In particular, in recent years, in order to prevent the effects of environmental degradation, the demand for hot-dip zinc-aluminum alloy plating with higher corrosion resistance has increased, and there are a wide variety of products that require hot-dip zinc-aluminum alloy plating. ing.
[0003]
As a general method of such hot dip zinc-aluminum alloy plating, there is a method called a two-bath method disclosed in Japanese Patent No. 2924894. This two-bath method is a method in which a steel material is immersed in a zinc bath and galvanized, and then the galvanized steel material is immersed again in a zinc-aluminum alloy bath for plating. As another method, a method of performing molten zinc-aluminum alloy plating of a steel material by a single dipping using a molten salt as a flux in a pretreatment stage of a steel material plating step has been put into practical use.
[0004]
[Problems to be solved by the invention]
However, the two-solution method of hot dip zinc-aluminum alloy plating requires two plating tanks, and there is a problem that the facility is large. Further, it is very difficult to perform zinc-aluminum alloy plating on a 10 m class large structure, and it is almost impossible to perform such plating in view of the finished quality. There is no plating tank that can handle 10m class large structures, and it is difficult to set plating conditions (plating temperature, immersion time) for large structures, and it can handle non-plating (no plating). (In the case of zinc plating, re-dipping is applied when non-plating occurs, but in the case of zinc-aluminum alloy, re-dipping does not result in plating, and the surface condition deteriorates.) .
[0005]
On the other hand, the method using the molten salt flux requires a step of pickling and removing the molten salt flux adhering to the plating surface, and requires a washing tank for that purpose. Therefore, it is necessary to make a corresponding capital investment, and there is a problem that efficiency decreases and costs increase due to an increase in the number of processes.
[0006]
Further, the hot dip galvanized layer applied to the steel material is strengthened by forming a zinc-iron alloy layer between the plated layer and the iron base by an alloying reaction of zinc and iron, and further, a zinc-aluminum alloy. By reacting with the molten metal, an aluminum-iron alloy layer and a zinc-aluminum-iron alloy layer are formed. Therefore, it is a problem how to react the hot dip galvanized layer and the molten zinc-aluminum alloy, but it is difficult to immerse the steel in the molten zinc-aluminum alloy as described above. Other methods are required.
[0007]
Therefore, in view of such a conventional problem, the present invention can prevent a decrease in efficiency and an increase in cost due to an increase in the number of processes, and can easily and reliably apply zinc-aluminum alloy plating to a large steel material. An object is to provide a zinc-aluminum alloy plating method.
[0008]
[Means for Solving the Problems]
As a result of diligent research to solve the above problems, the present inventors performed galvanization on the surface of the steel material in advance, heated the plated surface to a temperature at which the plated surface can react, By pouring the molten aluminum alloy, it was found that a highly corrosion-resistant aluminum-iron alloy layer and zinc-aluminum-iron alloy layer free from surface irregularities and burns were formed, and the present invention was completed.
[0009]
That is, in the hot dip zinc-aluminum alloy plating method according to the present invention, the surface of a steel material is galvanized and solidified, and then heated to a temperature (420 ° C.) or higher at which the plated layer can be in a molten state. holding, zinc on the surface of the steel zinc plated - characterized by sprinkle the molten aluminum alloy.
[0010]
In this molten zinc-aluminum alloy plating method, it is preferable that the molten zinc-aluminum molten metal contains 1 to 60 wt% of aluminum, and the balance contains zinc. Furthermore, it is preferable that the molten zinc-aluminum melt contains 0.1 to 3 wt% of at least one selected from Mg, Si, Ni and Bi. Moreover, it is preferable that the temperature of molten zinc-aluminum molten metal is 420-650 degreeC.
[0011]
DETAILED DESCRIPTION OF THE INVENTION
In the embodiment of the hot dip zinc-aluminum alloy plating method according to the present invention, after the galvanization is performed on the surface of the steel material and the plating is solidified, the temperature at which the zinc layer on the plating surface can be in a molten state (420 ° C. ) or higher. heated to and held in, zinc four hundred twenty to six hundred and fifty ° C. on the surface of the steel zinc plated - by subjecting pouring molten aluminum alloy, the molten zinc steel - subjecting an aluminum alloy plating.
[0012]
As a method of performing hot dip galvanizing on the outer surface of a steel pipe, a method of pouring molten zinc on the steel surface has already been proposed, but in the embodiment of the hot dip zinc-aluminum alloy plating method according to the present invention, it has been conventionally considered difficult. It is possible to continuously perform hot dip zinc-aluminum alloy plating of large structures and large steel pipes.
[0013]
In addition, in the conventional method of immersing the object to be plated in the molten zinc-aluminum alloy, the size of the object to be plated is limited by the size of the plating tank, but the hot dip zinc-aluminum alloy plating method according to the present invention is implemented. If it is the method of pouring a zinc-aluminum alloy molten metal like a form, it will become possible to apply | coat continuously, without being influenced by the magnitude | size of a plating tank.
[0014]
In the embodiment of the hot dip zinc-aluminum alloy plating method according to the present invention, after a normal hot dip galvanizing step such as degreasing, pickling, flux treatment, galvanizing, etc., a step of preheating and pouring molten zinc-aluminum alloy is performed. After that, wiping and cooling are performed to obtain a final product.
[0015]
In the embodiment of the hot dip zinc-aluminum alloy plating method according to the present invention, it is preferable that the hot dip zinc-aluminum molten metal contains 1 to 60 wt% of aluminum, and the balance contains zinc. The reason why the aluminum concentration is 1 to 60 wt% is that the corrosion resistance obtained is not changed when it exceeds 60 wt%, but the melting point of the alloy is increased due to the increase in concentration, while the workability is deteriorated. This is because the effect of maintaining the corrosion resistance is diminished.
[0016]
Furthermore, it is preferable that the molten zinc-aluminum melt contains 0.1 to 3 wt% of at least one selected from Mg, Si, Ni and Bi. The reason for adding Mg, Si, Ni, Bi is that workability, adhesion, hot water flowability, etc. are improved, and the reason for setting these concentrations to 0.1-3 wt% is 0.1 wt%. On the other hand, if the ratio is less than 3 wt%, the effect is reduced. On the other hand, if it exceeds 3 wt%, the workability is deteriorated and the quality is adversely affected (there may be cracking during bending, and the occurrence of sagging is also considered. )
[0017]
【Example】
Hereinafter, examples of the hot dip zinc-aluminum alloy plating method according to the present invention will be described in detail.
[0018]
[Example 1]
As a test piece, an SS material plate (100 × 70 × 3.2 mm) of a general structural material was prepared. This test piece is immersed in an aqueous NaOH solution at 70 ° C. for 10 minutes for degreasing, washed with water, immersed in an HC1 solution for 60 minutes, pickled, rinsed with water, immersed in a flux solution at 70 ° C. for 1 minute, and dried. And galvanizing was performed by immersing in a zinc bath at 440 to 470 ° C. for 5 to 10 minutes. In addition, the bath which melt | dissolved the electrolytic zinc ingot was used as a zinc bath.
[0019]
The galvanized plate was suspended in an electric heater and heated until the surface temperature reached 430 ° C. (a temperature at which the zinc layer on the plating surface could be in a molten state (420 ° C.) or higher).
[0020]
Next, a 420-450 ° C. molten zinc-aluminum alloy consisting of 5 wt% Al and the balance zinc was poured onto the plate taken out from the electric heater (contact time was about 10 seconds). In addition, the electrozinc ingot was used as zinc used for a zinc-aluminum alloy molten metal.
[0021]
Observation of the plating state of the plate plated with zinc-aluminum alloy in this way revealed that the surface was uneven, burned (due to the influence of impurities in the steel to be plated, the plating temperature being too high, etc. -The Fe alloy layer grew abnormally and the plated surface turned gray), and there was no unplating or sagging, and the plating state was good.
[0022]
[Example 2]
Except for pouring a 530-570 ° C molten zinc-aluminum alloy consisting of 30 wt% Al and the balance zinc, zinc-aluminum alloy plating was carried out in the same manner as in Example 1; No plating, no sagging, and no plating were observed.
[0023]
[Example 3]
Zinc-aluminum alloy plating was performed in the same manner as in Example 1 except that a molten zinc-aluminum alloy at 610 to 650 ° C. consisting of 55 wt% Al, 1.6 wt% Si, and the balance consisting of zinc was poured. However, there were no surface irregularities, burns, non-plating, or sagging, and the plating state was good.
[0024]
[Example 4]
Zinc-aluminum alloy plating was performed in the same manner as in Example 1 except that 5 wt% Al, 1 wt% Mg, and the balance zinc-aluminum molten metal were poured. No plating, no sagging, and no plating were observed.
[0025]
[Example 5]
Zinc-aluminum alloy plating was performed in the same manner as in Example 1 except that 5 wt% Al, 1 wt% Ni, and the balance zinc-aluminum molten metal was poured. No plating, no sagging, and no plating were observed.
[0026]
[Example 6]
Zinc-aluminum alloy plating was performed in the same manner as in Example 1 except that 5 wt% Al, 1 wt% Bi, and the balance zinc-aluminum molten metal was poured. No plating, no sagging, and no plating were observed.
[0027]
【The invention's effect】
As described above, according to the hot dip zinc-aluminum alloy plating method of the present invention, it is possible to prevent a decrease in efficiency and an increase in cost due to an increase in the number of steps, and to easily and reliably apply zinc-aluminum alloy plating to large steel materials. Can do.

Claims (5)

鋼材の表面に亜鉛めっきを施し、このめっきを凝固させた後、このめっき層が溶融状態になり得る温度以上に加熱して保持亜鉛めっきが施された鋼材の表面に亜鉛−アルミニウム合金溶湯を注ぎかけることを特徴とする、溶融亜鉛−アルミニウム合金めっき方法。After galvanizing the surface of the steel material and solidifying the plating, the galvanized layer is heated to a temperature higher than the temperature at which it can be melted and held, and the zinc-aluminum alloy molten metal is applied to the surface of the galvanized steel material. A hot dip zinc-aluminum alloy plating method, wherein: 前記溶融亜鉛−アルミニウム溶湯が、1〜60wt%のアルミニウムを含み、残部として亜鉛を含むことを特徴とする、請求項1に記載の溶融亜鉛−アルミニウム合金めっき方法。2. The hot dip zinc-aluminum alloy plating method according to claim 1, wherein the molten zinc-aluminum molten metal contains 1 to 60 wt% of aluminum, and the remainder contains zinc. 前記溶融亜鉛−アルミニウム溶湯が、Mg、Si、NiおよびBiから選ばれた少なくとも1種以上を0.1〜3wt%含むことを特徴とする、請求項2に記載の溶融亜鉛−アルミニウム合金めっき方法。The molten zinc-aluminum alloy plating method according to claim 2, wherein the molten zinc-aluminum molten metal contains 0.1 to 3 wt% of at least one selected from Mg, Si, Ni and Bi. . 前記めっき表面の亜鉛層が溶融状態になり得る温度が420℃あることを特徴とする、請求項1乃至3のいずれかに記載の溶融亜鉛−アルミニウム合金めっき方法。The hot dip zinc-aluminum alloy plating method according to any one of claims 1 to 3 , wherein a temperature at which the zinc layer on the plating surface can be in a molten state is 420 ° C. 前記溶融亜鉛−アルミニウム溶湯の温度が420〜650℃であることを特徴とする、請求項1乃至4のいずれかに記載の溶融亜鉛−アルミニウム合金めっき方法。The hot-dip zinc-aluminum alloy plating method according to any one of claims 1 to 4, wherein the molten zinc-aluminum molten metal has a temperature of 420 to 650 ° C.
JP2002243391A 2002-08-23 2002-08-23 Hot-dip zinc-aluminum alloy plating method Expired - Fee Related JP3811109B2 (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP2002243391A JP3811109B2 (en) 2002-08-23 2002-08-23 Hot-dip zinc-aluminum alloy plating method

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP2002243391A JP3811109B2 (en) 2002-08-23 2002-08-23 Hot-dip zinc-aluminum alloy plating method

Publications (2)

Publication Number Publication Date
JP2004083950A JP2004083950A (en) 2004-03-18
JP3811109B2 true JP3811109B2 (en) 2006-08-16

Family

ID=32052165

Family Applications (1)

Application Number Title Priority Date Filing Date
JP2002243391A Expired - Fee Related JP3811109B2 (en) 2002-08-23 2002-08-23 Hot-dip zinc-aluminum alloy plating method

Country Status (1)

Country Link
JP (1) JP3811109B2 (en)

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN106001106A (en) * 2016-05-24 2016-10-12 江苏金基特钢有限公司 Preparation method of anti-corrosion steel wire

Families Citing this family (8)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JP4589822B2 (en) * 2004-08-19 2010-12-01 新日本製鐵株式会社 Road snow melting panels
IN2012DN02563A (en) * 2009-08-28 2015-08-28 Daiwa Steel Tube Ind
JP5886114B2 (en) * 2012-04-18 2016-03-16 株式会社デンロコーポレーション Zn-Al alloy plating method
JP5961433B2 (en) * 2012-04-18 2016-08-02 株式会社竹中工務店 Method for producing Zn-Al alloy plated reinforcing bar
JP6065043B2 (en) * 2014-04-23 2017-01-25 Jfeスチール株式会社 Molten Al-Zn-based plated steel sheet and method for producing the same
CN104959397A (en) * 2015-06-29 2015-10-07 江苏金基特钢有限公司 Manufacturing method of corrosion-resistant steel wire
CN108486520B (en) * 2018-05-29 2020-07-28 佛山市高明利钢精密铸造有限公司 Preparation method of aluminized steel with high-density aluminized layer
CN114959538A (en) * 2022-06-14 2022-08-30 常州大学 Zinc-aluminum in-situ gradient coating on surface of iron alloy and preparation method thereof

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN106001106A (en) * 2016-05-24 2016-10-12 江苏金基特钢有限公司 Preparation method of anti-corrosion steel wire

Also Published As

Publication number Publication date
JP2004083950A (en) 2004-03-18

Similar Documents

Publication Publication Date Title
JP3770875B2 (en) Flux and method for hot dip galvanizing
KR101642305B1 (en) Flux and fluxing bath for hot dip galvanization, process for the hot dip galvanization of an iron or steel article
JP5824868B2 (en) Method for producing zinc-based plated steel material or zinc-based plated steel molded product
CN107904532A (en) A kind of method for constructing the double coating of high anti-corrosion kirsite in steel surface
JP3811109B2 (en) Hot-dip zinc-aluminum alloy plating method
JP4970231B2 (en) Hot-dip galvanized steel and its manufacturing method
JP3080014B2 (en) Hot-dip plating method
JPS6138259B2 (en)
CN110777316B (en) Rare earth alloy hot-dip coating steel plate and production method thereof
JPS6260854A (en) Manufacture of screw thread product
JP2004244650A (en) METHOD OF PRODUCING Zn-Al-Mg BASED ALLOY PLATED STEEL
JP4337653B2 (en) Hot-dip galvanized steel and method for producing the same
KR100436597B1 (en) Method for plating with molten aluminum
JPH04214848A (en) Hot-dip galvanized coating material and method for hot-dip galvanizing
JPH06279968A (en) Aluminum-zinc alloy plating method for iron and steel products
JPH0472047A (en) Aluminum/zinc alloy hot-dip coated material and aluminum/zinc alloy hot-dip coating method
JPH0860329A (en) Production of galvannealed steel sheet
JPS59226163A (en) Surface treatment for providing corrosion resistance
JP2982653B2 (en) High corrosion resistance Al-Zn alloy hot-dip coated steel sheet and manufacturing method thereof
JP3494134B2 (en) Hot-dip plating method
JPH116047A (en) Base metal for hot dip zinc alloy coating bath, hot dip coating bath, hot dip zinc alloy coated steel and its production
JPH02243793A (en) Production of tin and tin alloy plated material
JP4899030B2 (en) Flux and hot dip zinc-aluminum alloy plating method.
JPS60125361A (en) Flux composition for zinc alloy hot dipping
JPH04176852A (en) Aluminum-zinc alloy hot-dipping method

Legal Events

Date Code Title Description
A621 Written request for application examination

Free format text: JAPANESE INTERMEDIATE CODE: A621

Effective date: 20050525

A977 Report on retrieval

Free format text: JAPANESE INTERMEDIATE CODE: A971007

Effective date: 20060130

A131 Notification of reasons for refusal

Free format text: JAPANESE INTERMEDIATE CODE: A131

Effective date: 20060207

A521 Written amendment

Free format text: JAPANESE INTERMEDIATE CODE: A523

Effective date: 20060322

TRDD Decision of grant or rejection written
A01 Written decision to grant a patent or to grant a registration (utility model)

Free format text: JAPANESE INTERMEDIATE CODE: A01

Effective date: 20060523

A61 First payment of annual fees (during grant procedure)

Free format text: JAPANESE INTERMEDIATE CODE: A61

Effective date: 20060525

R150 Certificate of patent or registration of utility model

Free format text: JAPANESE INTERMEDIATE CODE: R150

FPAY Renewal fee payment (event date is renewal date of database)

Free format text: PAYMENT UNTIL: 20090602

Year of fee payment: 3

S111 Request for change of ownership or part of ownership

Free format text: JAPANESE INTERMEDIATE CODE: R313111

FPAY Renewal fee payment (event date is renewal date of database)

Free format text: PAYMENT UNTIL: 20090602

Year of fee payment: 3

R350 Written notification of registration of transfer

Free format text: JAPANESE INTERMEDIATE CODE: R350

FPAY Renewal fee payment (event date is renewal date of database)

Free format text: PAYMENT UNTIL: 20100602

Year of fee payment: 4

FPAY Renewal fee payment (event date is renewal date of database)

Free format text: PAYMENT UNTIL: 20100602

Year of fee payment: 4

FPAY Renewal fee payment (event date is renewal date of database)

Free format text: PAYMENT UNTIL: 20110602

Year of fee payment: 5

FPAY Renewal fee payment (event date is renewal date of database)

Free format text: PAYMENT UNTIL: 20110602

Year of fee payment: 5

FPAY Renewal fee payment (event date is renewal date of database)

Free format text: PAYMENT UNTIL: 20120602

Year of fee payment: 6

FPAY Renewal fee payment (event date is renewal date of database)

Free format text: PAYMENT UNTIL: 20120602

Year of fee payment: 6

FPAY Renewal fee payment (event date is renewal date of database)

Free format text: PAYMENT UNTIL: 20130602

Year of fee payment: 7

R250 Receipt of annual fees

Free format text: JAPANESE INTERMEDIATE CODE: R250

LAPS Cancellation because of no payment of annual fees