JPS5974252A - Zn alloy for hot dipping with high corrosion resistance - Google Patents
Zn alloy for hot dipping with high corrosion resistanceInfo
- Publication number
- JPS5974252A JPS5974252A JP18355282A JP18355282A JPS5974252A JP S5974252 A JPS5974252 A JP S5974252A JP 18355282 A JP18355282 A JP 18355282A JP 18355282 A JP18355282 A JP 18355282A JP S5974252 A JPS5974252 A JP S5974252A
- Authority
- JP
- Japan
- Prior art keywords
- alloy
- corrosion resistance
- hot
- layer
- hot dipping
- 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.)
- Granted
Links
Landscapes
- Coating With Molten Metal (AREA)
Abstract
Description
【発明の詳細な説明】
この発明は、特に鉄鋼材料の表面を溶融メッキすること
によって、耐食性にすぐれ、かつ曲げ加工を施してもメ
ッキ層に剥離や割れ発生のない材料を得るための溶融メ
ッキ用高耐食性Zn合金に関するものである。DETAILED DESCRIPTION OF THE INVENTION This invention is a method for hot-dip plating to obtain a material that has excellent corrosion resistance and does not peel or crack even when subjected to bending, by hot-dip plating the surface of a steel material. This invention relates to a highly corrosion-resistant Zn alloy for use.
一般に、鉄鋼材料の耐食性を向上させるための安価にし
て簡便な方法として、その表面にZnまたはZn合金を
溶融メッキする方法が知られており。Generally, a method of hot-dip plating Zn or a Zn alloy on the surface of a steel material is known as an inexpensive and simple method for improving the corrosion resistance of a steel material.
かつ溶融メッキ用Zn合金として数多くのものが提案さ
れている。確かに、これらの従来Zn合金の溶融メッキ
によって鉄鋼材料は比較的良好な耐食性をもつようにな
ったが、これが苛酷な使用環境におかれた場合、必ずし
も十分満足する耐食性を示すものではなく、さらに通常
、素地とメッキ層間には脆いFe −Zn系合金層が形
成されているので、これに曲げ加工を施すと、メッキ層
に剥離や割れが発生するのを避けることができないもの
であった。In addition, many Zn alloys for hot-dip plating have been proposed. It is true that these conventional hot-dip coatings of Zn alloys have provided steel materials with relatively good corrosion resistance, but they do not necessarily show sufficient corrosion resistance when placed in harsh usage environments. Furthermore, since a brittle Fe-Zn alloy layer is usually formed between the base material and the plating layer, when this is subjected to bending, it is unavoidable that the plating layer will peel or crack. .
そこで、本発明者等は、上述のような観点から、苛酷な
使用条件下におかれてもすぐれた耐食性を示し、かつ曲
げ加工を施してもメッキ層に剥離や割れの発生がない溶
融メッキ製品を確実容易に得べく、特に溶融メッキ用Z
n合金について研究を行なった結果、ZnにMnヲ含有
させると、 Znと結合して形成したZn−Mn合金は
T1との相溶性が良いことからZn中のT1含有量域が
拡大されるようになり、さらにMnにはT1化合物を均
一に分散析出せしめる杼用があるほか、合金自体の結晶
粒を微細化する作用があシ、しかもこのようにMnの含
有によってT1含有量が増大し、かつ結晶粒の微細化し
たZn合金は著しくすぐれた耐食性をもつようになり、
また、一方Mおよび必要に応じてさらにSiミラ有させ
ると、メッキ層と素地間のFe−Zn系合金層の形成が
著しく抑制されるようになシ、曲げ加工時に前記Fe−
Zn系合金層が原因のメッキ層剥離やメッキ層に割れが
生ずる現象が皆無となるという知見を得たのである。Therefore, from the above-mentioned viewpoints, the present inventors developed a hot-dip coating that exhibits excellent corrosion resistance even under harsh usage conditions and that does not cause peeling or cracking in the plated layer even when subjected to bending. In order to obtain products reliably and easily, especially Z for hot-dip plating.
As a result of research on n alloys, it was found that when Mn is added to Zn, the Zn-Mn alloy formed by combining with Zn has good compatibility with T1, so the range of T1 content in Zn is expanded. In addition, Mn acts as a shuttle to disperse and precipitate T1 compounds uniformly, and also has the effect of refining the crystal grains of the alloy itself.Moreover, the T1 content increases due to the inclusion of Mn, In addition, Zn alloys with finer grains have significantly better corrosion resistance.
On the other hand, if M and optionally further include a Si mirror, the formation of an Fe-Zn alloy layer between the plating layer and the substrate can be significantly suppressed.
It has been found that there is no phenomenon of peeling of the plating layer or cracking of the plating layer caused by the Zn-based alloy layer.
したがって、この発明は上記知見にもとづいてなされた
ものであって、溶融メッキ用Zn合金を、Ti: 0.
1〜2.0 %、 Mn: 0.1〜3.0 % 、
M : 0.1〜1.64 e含有し、さらに必要に応
じてS、i : 0.01〜0.4 % k含有し、残
シがZnと不可避不純物からなる組成C以上重量係)で
構成し、このZn合金を、特に鉄鋼材料の表面に溶融メ
ッキすることによって、苛酷な腐食環境下での長期に亘
っての安定した使用と、メッキ層剥離や割れの発生のな
い曲げ加工を可能とした点に特徴を有するものである。Therefore, the present invention has been made based on the above knowledge, and a Zn alloy for hot-dip plating with Ti: 0.
1-2.0%, Mn: 0.1-3.0%,
Contains M: 0.1 to 1.64% and further contains S, i: 0.01 to 0.4% K as necessary, and the remainder is Zn and unavoidable impurities. By hot-dipping this Zn alloy, especially on the surface of steel materials, it is possible to use it stably over a long period of time in harsh corrosive environments and to perform bending without peeling or cracking of the plating layer. It is characterized by the following points.
つぎに、この発明のZn合金の成分組成範囲を上記の通
シに限定した理由を説明する。Next, the reason why the composition range of the Zn alloy of the present invention is limited to the above-mentioned range will be explained.
0)T1
Ti成分には、苛酷な腐食環境下でも十分満足するすぐ
れた耐食性を付与する作用がるるか、その含有量がO1
111係では所望のすぐれた耐食性を確保することがで
きず、一方2.0%を越えて含有させると、メッキ作業
性が損なわれるようになり、したがってメッキ作業性を
良好な状態に保持するには溶融メッキ浴温度をかなり高
くしなければならず、この結果被メッキ材がメッキ浴中
に溶解して浴組成を著しく乱すようになることから、そ
の含有量ヲ0.1〜2,0%と定めた。なお、0.45
〜1.20係の含有が望ましい。0) T1 Does the Ti component have the effect of imparting excellent corrosion resistance that satisfies even in severe corrosive environments?
111 cannot secure the desired excellent corrosion resistance, and on the other hand, if the content exceeds 2.0%, the plating workability will be impaired, and therefore it will be difficult to maintain the plating workability in a good state. The temperature of the hot-dip plating bath must be raised considerably, and as a result, the material to be plated dissolves in the plating bath and significantly disturbs the bath composition. It was determined that In addition, 0.45
The content is preferably 1.20%.
(b) Mn
Mn成分には、上記のようにZn素地中へのT1の固溶
度を高め、かつ結晶粒および一部分散析出するTi化合
物を微細化すると共に、前記T1化合物の均−分布全は
かり、もって耐食性を向上させる作用があるが、その含
有量が0.1係未満では前記作用に所望の効果が得られ
ず、一方3.0 qb’を越えて含有させると合金の靭
性が極端に劣化するようになってメッキ層に亀裂や剥離
が生じ易くなることから、その含有量全0.1〜3.0
係と定めた。なお、0.4〜1.8係の含有が望ましい
。(b) Mn As mentioned above, the Mn component increases the solid solubility of T1 in the Zn matrix, refines the crystal grains and partially dispersed precipitated Ti compounds, and improves the uniform distribution of the T1 compound throughout the whole. It has the effect of improving corrosion resistance, but if the content is less than 0.1 qb', the desired effect will not be obtained, while if the content exceeds 3.0 qb', the toughness of the alloy will be extremely reduced. The total content is 0.1 to 3.0 because the plating layer tends to deteriorate and cracks and peels.
The person in charge was appointed as the person in charge. Note that the content is preferably 0.4 to 1.8%.
(c) AA
M成分には、上記のように溶融メッキ時に素地の表面部
とメッキ層との間に脆いFe −Zn系合金層が形成さ
れるのを抑制し、もって曲げ加工時に前記Fe −Zn
系合金層が原因のメッキ層の剥離および割れを防止し、
かつMn含有によるメッキ層の硬化を緩和する作用があ
るが、その含有量が0.1係未満では前記作用に所望の
効果が得られず、一方1.6elIを越えて含有させる
と、耐食性が低下するようになることから、その含有量
’e0.1〜1.6係と定めた。なお、0.3〜0.8
係の含有が望ましい。(c) As mentioned above, the AA M component suppresses the formation of a brittle Fe-Zn alloy layer between the surface of the substrate and the plating layer during hot-dip plating, and thereby suppresses the formation of the Fe-Zn alloy layer during bending. Zn
Prevents peeling and cracking of the plating layer caused by the alloy layer,
It also has the effect of mitigating the hardening of the plating layer due to Mn content, but if the Mn content is less than 0.1%, the desired effect cannot be obtained, while if the Mn content exceeds 1.6elI, the corrosion resistance will be reduced. Therefore, the content was determined to be between 0.1 and 1.6. In addition, 0.3 to 0.8
It is desirable to include a person in charge.
(a)SI
SI成分には、メッキ浴の流動性を向上させて平滑な光
沢のあるメッキ層を形成するほか、Fe−Zn合金層の
形成を一段と抑制し、かつ耐食性を飛躍的に向上させる
作用があるので、特にこれらの特性が要求される場合に
必要に応じて含有されるが、その含有量がo、ois未
満では前記作用に所望の向上効果が得られず、一方0.
4 % ’i越えて含有させるとメッキ性が損なわれる
ようになることから、その含有量を0.01〜0.4係
と定めた。なお、0.03〜0.20%の含有が望まし
い。(a) SI The SI component not only improves the fluidity of the plating bath to form a smooth and glossy plating layer, but also further suppresses the formation of the Fe-Zn alloy layer and dramatically improves corrosion resistance. Since it has a certain effect, it is included as necessary especially when these properties are required. However, if the content is less than o, ois, the desired effect of improving the above effect cannot be obtained; on the other hand, if the content is less than o.
If the content exceeds 4%'i, the plating properties will be impaired, so the content was set at 0.01 to 0.4. Note that the content is preferably 0.03 to 0.20%.
つぎに、この発明のZn合金を実施例により比較例と対
比しながら説明する。Next, the Zn alloy of the present invention will be explained using examples and comparing with comparative examples.
実施例
それぞれ第1表に示される成分組成をもった本発明Zn
合金1〜25.比較Zn合金1〜4.および純Znの溶
融メッキ浴を調製し、ついでメッキ浴温をそれぞれ46
0〜560℃の温度範囲内の所定温度に保持した前記溶
融メッキ浴中に、それぞれZnC42−NH4Ct系フ
ラックスで前処理した厚さ0.4調を有する鋼板を5秒
間浸漬し、該鋼板表面に片面厚さ210μmのメッキ層
を形成することによって本発明Zn合金メッキ鋼板1〜
25.比較Zn合金メッキ鋼板1〜4.および従来Zn
メッキ鋼板をそれぞれ製造した。なお、比較Zn合金1
〜4は。The present invention Zn having the component composition shown in Table 1 for each example
Alloys 1-25. Comparative Zn alloys 1 to 4. and pure Zn hot-dip plating baths, and then the plating bath temperature was set to 46
A steel plate having a thickness of 0.4 and pretreated with ZnC42-NH4Ct-based flux was immersed for 5 seconds in the hot-dip plating bath maintained at a predetermined temperature within the temperature range of 0 to 560°C, and the surface of the steel plate was coated. By forming a plating layer with a thickness of 210 μm on one side, the Zn alloy plated steel sheet 1 of the present invention
25. Comparative Zn alloy plated steel sheets 1 to 4. and conventional Zn
Each plated steel plate was manufactured. In addition, comparison Zn alloy 1
~4 is.
いずれも構成成分のうちのいずれかの成分含有量(第1
表に※印?付したもの)がこの発明の範囲から外れた組
成をもつものである。In both cases, the content of one of the constituent components (first
Marked with * on the front? (as shown in the figure) have a composition outside the scope of this invention.
ついで、この結果得られた本発明Zn合金メッキ鋼板1
〜25.比較Zn合金メッキ鋼板1〜4.および従来Z
nメッキ鋼板について、Fe−Zn系合金層の有無を観
察すると共に、J工S −Z2371にもとづく塩水噴
霧試験、並びK J I S −Z224BVCもとづ
く曲げ試験を行ない、前記塩水噴霧試験では鋼板メッキ
面に赤錆が発生するまでの時間を測定し、また前記曲げ
試験では曲げ面におけるメッキ層の状態を観察し、メッ
キ層に剥離も割れも全く発生(−でいない場合をO印、
メッキ層に剥離および割れがはっきりと認められる場合
をX印でそれぞれ評価した。これらの測定結果を第1表
に合せて示した。Next, the resulting Zn alloy plated steel sheet 1 of the present invention
~25. Comparative Zn alloy plated steel sheets 1 to 4. and conventional Z
In addition to observing the presence or absence of an Fe-Zn alloy layer, the n-plated steel sheet was subjected to a salt spray test based on J Engineering S-Z2371 and a bending test based on K J I S-Z224BVC. In addition, in the bending test, the state of the plating layer on the bent surface was observed, and there was no peeling or cracking in the plating layer (marked O if there was no negative sign).
Cases in which peeling and cracking were clearly observed in the plating layer were evaluated with an X mark. These measurement results are also shown in Table 1.
第1表に示される結果から、本発明Zn合金1〜25に
よってそれぞれ本発明Zn合金メッキ鋼板1〜25は、
いずれもすぐれた耐食性を示すと共に、曲げ加工を施し
ても剥離や割れの全く発生しない密着性のよいメッキ層
を有しているのに対して、構成成分のうちのいずれかの
成分含有量がこの発明の範囲から外れた組成を有する比
較Zn合金1〜4によって、それぞれ溶融メッキされた
比較Zn合金メッキ鋼板1〜4においては、耐食性9合
金層の形成、および曲げ評価のうちの少なくとも1つの
点で劣った結果を示している。さらに純Znf溶融メン
キした従来Znメッキ鋼板においても、 Fe−Zn系
合金層の形成があり、かつ耐食性およびメッキ層密着性
の著しく劣ったものになっている。また本発明Zn合金
メッキ鋼板1〜6に見られるように、所定量のMnおよ
びAtの存在の下でT1含有量が多くなればなるほど耐
食性がすぐれたものになることが明らかである。From the results shown in Table 1, according to the Zn alloys 1 to 25 of the present invention, the Zn alloy plated steel sheets 1 to 25 of the present invention were
All of them show excellent corrosion resistance and have a plating layer with good adhesion that does not peel or crack even when subjected to bending. Comparative Zn alloy plated steel sheets 1 to 4 each hot-dip plated with Comparative Zn alloys 1 to 4 having compositions outside the scope of the present invention were tested in at least one of the formation of a corrosion-resistant 9 alloy layer and the bending evaluation. It shows inferior results in points. Furthermore, even in conventional Zn-plated steel sheets that have been melt coated with pure Zn, a Fe--Zn alloy layer is formed, and the corrosion resistance and adhesion of the plating layer are extremely poor. Furthermore, as seen in Zn alloy plated steel sheets 1 to 6 of the present invention, it is clear that the higher the T1 content in the presence of predetermined amounts of Mn and At, the better the corrosion resistance becomes.
また、本発明Zn合金を溶融メッキした上に、さらにク
ロメート処理を施すと、一段と耐食性が向上するように
なることが確認された。Furthermore, it was confirmed that when the Zn alloy of the present invention was hot-dipped and further subjected to chromate treatment, the corrosion resistance was further improved.
上述のように、この発明の溶融メッキ用高耐食性Zn台
舎によれば、特に鉄鋼材料の表面を溶融メンキすること
により、苛酷な使用条件におかれてもすぐれた耐食性を
確保することができ、かつ鉄鋼材料表面への密着性がき
わめて良く、脆いFe−Zn系合金層の形成がほとんど
ないので1曲げ加工時にメッキ層に剥離や割れの発生が
皆無となるなど工業上有用な効果がもたらされるのであ
る。As mentioned above, according to the highly corrosion-resistant Zn stand for hot-dip plating of the present invention, excellent corrosion resistance can be ensured even under severe usage conditions, especially by hot-dip coating the surface of the steel material. , and has extremely good adhesion to the surface of steel materials, with almost no formation of a brittle Fe-Zn alloy layer, resulting in industrially useful effects such as no peeling or cracking of the plating layer during one bending process. It is possible.
出願人 長 堀 貞 治 出願人 大 島 正 則 代理人 富 1)和 夫Applicant Sadaharu Nagahori Applicant Masanori Oshima Agent Tomi 1) Kazuo
Claims (2)
0.1〜3.0 %’、 At!二0.1〜1.6%を
含有し、残りがZnと不可避不純物からなる組成C以上
重量幅)を有することを特徴とする溶融メッキ用高耐食
性Zn合金。(1) Ti': 0.1-2.0%, Mn:
0.1-3.0%', At! 2. A highly corrosion-resistant Zn alloy for hot-dip plating, characterized in that it has a composition C or more (weight range) containing 0.1 to 1.6% of Zn and the remainder consisting of Zn and unavoidable impurities.
.1〜3.0 %、 Ml:0.1〜1.6係、Si:
0.01〜0.4チを含有し、残りがZnと不可避不純
物からなる組成(以上重量幅)を有することを特徴とす
る溶融メッキ用高耐食性Zn合金。(2) Ti: 0.1-2.0%, Mn: 0
.. 1-3.0%, Ml: 0.1-1.6%, Si:
A highly corrosion-resistant Zn alloy for hot-dip plating, characterized in that it contains 0.01 to 0.4% Zn, and the remainder consists of Zn and unavoidable impurities (the above weight range).
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP18355282A JPS6056776B2 (en) | 1982-10-19 | 1982-10-19 | Highly corrosion resistant Zn alloy for hot-dip plating |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP18355282A JPS6056776B2 (en) | 1982-10-19 | 1982-10-19 | Highly corrosion resistant Zn alloy for hot-dip plating |
Publications (2)
Publication Number | Publication Date |
---|---|
JPS5974252A true JPS5974252A (en) | 1984-04-26 |
JPS6056776B2 JPS6056776B2 (en) | 1985-12-11 |
Family
ID=16137796
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
JP18355282A Expired JPS6056776B2 (en) | 1982-10-19 | 1982-10-19 | Highly corrosion resistant Zn alloy for hot-dip plating |
Country Status (1)
Country | Link |
---|---|
JP (1) | JPS6056776B2 (en) |
Cited By (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPS61199063A (en) * | 1985-02-28 | 1986-09-03 | Sadaji Nagabori | Zn alloy for hot dipping having superior corrosion resistance and high workability |
JPS61201743A (en) * | 1985-03-04 | 1986-09-06 | Sadaji Nagabori | Manufacture of zn alloy for hot dipping having superior corrosion resistance and high workability |
-
1982
- 1982-10-19 JP JP18355282A patent/JPS6056776B2/en not_active Expired
Cited By (4)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPS61199063A (en) * | 1985-02-28 | 1986-09-03 | Sadaji Nagabori | Zn alloy for hot dipping having superior corrosion resistance and high workability |
JPH0414174B2 (en) * | 1985-02-28 | 1992-03-12 | Sadaji Nagabori | |
JPS61201743A (en) * | 1985-03-04 | 1986-09-06 | Sadaji Nagabori | Manufacture of zn alloy for hot dipping having superior corrosion resistance and high workability |
JPH0135057B2 (en) * | 1985-03-04 | 1989-07-24 | Sadaji Nagabori |
Also Published As
Publication number | Publication date |
---|---|
JPS6056776B2 (en) | 1985-12-11 |
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