JPH01184242A - Titanium alloy having excellent ductility - Google Patents
Titanium alloy having excellent ductilityInfo
- Publication number
- JPH01184242A JPH01184242A JP770088A JP770088A JPH01184242A JP H01184242 A JPH01184242 A JP H01184242A JP 770088 A JP770088 A JP 770088A JP 770088 A JP770088 A JP 770088A JP H01184242 A JPH01184242 A JP H01184242A
- Authority
- JP
- Japan
- Prior art keywords
- ductility
- titanium alloy
- alloy
- room temperature
- phase
- 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
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- Shaping Metal By Deep-Drawing, Or The Like (AREA)
Abstract
Description
【発明の詳細な説明】
〈産業上の利用分野〉
この発明は、常温における成形加工が可能な延性に優れ
たチタン合金に関するものである。DETAILED DESCRIPTION OF THE INVENTION <Industrial Application Field> The present invention relates to a titanium alloy with excellent ductility that can be formed at room temperature.
〈背景技術〉
チタンの特性である優れた比強度、耐食性、耐熱性等が
注目され、これまでに数多くのチタン合金が開発されて
きたが、それでもその用途は航空機関係や化学装置類関
係を中心とした極めて限られた分野に止まっているのが
現状である。<Background technology> The characteristics of titanium, such as its excellent specific strength, corrosion resistance, and heat resistance, have attracted attention, and many titanium alloys have been developed to date. The current situation is that it is limited to an extremely limited field.
このようにチタン合金の需要拡大が遅々として進展しな
い要因は、チタン合金が一般に高価であることもさるこ
とながら、延性が非常に乏しく、板材としてもプレス成
形等による常温での成形加工ができないと言う点が挙げ
られる。The reason why the demand for titanium alloys has been slow to expand is that titanium alloys are generally expensive, but they also have very poor ductility and cannot be formed into sheet materials at room temperature by press forming, etc. The following points can be mentioned.
例えば、最も一般的なチタン合金であるTi−6pJL
−4V合金は常温での伸びが高々lO%程度に過ぎず、
従ってTi−6AR−4V合金製板材を常温で成形加工
することは全く不可能であった。For example, Ti-6pJL, the most common titanium alloy
-4V alloy has an elongation of only about 10% at room temperature,
Therefore, it was completely impossible to form a Ti-6AR-4V alloy plate material at room temperature.
更に、延性改善を主目的として最近開発されたTi−1
5V−3AI−3Sn−3Cr合金(β型チタン合金)
でさえも常温における伸びは20%程度でしかなく、常
温での成形加工用として供するには延性が不十分と言わ
ざるを得なかった。Furthermore, Ti-1, which was recently developed with the main purpose of improving ductility,
5V-3AI-3Sn-3Cr alloy (β-type titanium alloy)
Even so, the elongation at room temperature was only about 20%, and it had to be said that the ductility was insufficient to be used for molding at room temperature.
〈問題点を解決するための手段〉
そこで本発明者等は、板材として常温での成形加工を施
すことも可能な優れた延性を示すチタン合金を提供すべ
く、特に、「結晶構造が稠密六方晶であるα型、結晶構
造が体心立方晶であるβ型及び2相が混合したα/β型
の3つに分類されるチタン合金の中でも、−船釣に常温
での延性はβタイプが優れている」との事実に着目し、
このβ型チタン合金の更なる延性改善の可能性を求めて
その塑性変形挙動を詳細に検討したところ、[β型チタ
ン合金の延性はβ相の安定度と密接に関連しており、β
相を準安定な状態とした上で、これに適度のAl、 Z
r、 Snの一種又は2種以上を添加すると、この合金
を組成変形させた場合にマルテンサイト変態を伴う所謂
“変態誘起塑性(TRIP)”が現出され、大幅に改善
された延性を示すようになる」との知見が得られたので
ある。<Means for Solving the Problems> Therefore, in order to provide a titanium alloy that exhibits excellent ductility and can be formed into a sheet material at room temperature, the present inventors particularly focused on Among titanium alloys, which are classified into three types: α type, which has a body-centered cubic crystal structure, β type, which has a body-centered cubic crystal structure, and α/β type, which has a mixed two-phase crystal structure, β type has ductility at room temperature for boat fishing. Focusing on the fact that
In search of the possibility of further improving the ductility of this β-type titanium alloy, we investigated its plastic deformation behavior in detail and found that [the ductility of β-type titanium alloy is closely related to the stability of the β phase;
After making the phase metastable, appropriate amounts of Al and Z are added to it.
When one or more types of r and Sn are added, so-called "transformation-induced plasticity (TRIP)" accompanied by martensitic transformation appears when this alloy is compositionally deformed, and it appears to exhibit significantly improved ductility. We obtained the knowledge that ``it becomes ``.
この発明は、上記知見に基づいてなされたものであり、
[チタン合金を、7216〜20%(以降、成分割合を
示す%は重量%とする)を含有量すると共に、更に
AI!:2%以下。This invention was made based on the above knowledge, and includes a titanium alloy containing 7216 to 20% (hereinafter, the percentage indicating the component ratio is expressed as weight%), and further AI! : 2% or less.
Zr:6%以下。Zr: 6% or less.
Sn:6%以下
のうちの1種以上をも含み、残部が実質的にTjから成
る成分組成に構成することによって、極めて優れた延性
を備えしめた点」に特徴を有するものである。It is characterized by having extremely excellent ductility by configuring the composition to include one or more of Sn: 6% or less, and the remainder being substantially Tj.
次に、この発明において合金の成分組成を前記の如くに
限定した理由を説明する。Next, the reason why the composition of the alloy is limited as described above in this invention will be explained.
(a+ V
■成分にはβ相を安定化する作用があり、その含有量は
β相を準安定な状態に保つ上で非常に重要である。即ち
、■含有量が16%未満では合金組織が常温においてβ
単相とはならず、このためチタン合金に十分な延性を付
与することができない。一方、20%を越えて■を含有
させると、今度はβ相が安定化し過ぎて加工誘起マルテ
ンサイト変態が生じなくなってやはり延性が劣化してし
まう。従って、■含有量は16〜20%と限定し=3−
た。(a+ V The ■ component has the effect of stabilizing the β phase, and its content is very important in keeping the β phase in a metastable state. In other words, if the ■ content is less than 16%, the alloy structure is β at room temperature
It does not form a single phase, and therefore, sufficient ductility cannot be imparted to the titanium alloy. On the other hand, if the content exceeds 20%, the β phase becomes too stable, deformation-induced martensitic transformation no longer occurs, and ductility deteriorates as well. Therefore, the content was limited to 16-20% = 3-.
(b) 八fl、 Zr、及びSn
これらの成分は、微量添加によっても■含有量が調整さ
れたβ型チタン合金の延性を一段と改善する作用があり
、常温で十分な延性を確保するためには1種又は2種以
上の添加が欠かせないものであるが、以下、その含有量
の限定理由を個々の成分別に説明する。(b) 8fl, Zr, and Sn These components have the effect of further improving the ductility of the β-type titanium alloy whose content has been adjusted even when added in small amounts, and in order to ensure sufficient ductility at room temperature. Although it is essential to add one or more types of these, the reason for limiting the content will be explained for each individual component below.
Apには加工誘起マルテンサイト変態を阻害するω相の
析出を抑制することで変態誘起塑性(TRIP)を出現
させる重要な作用がある。しかしながら、2%を越えて
含有させるとマルテンサイト変態における剪断抵抗を高
め、逆に加工誘起マルテンサイト変態を抑制して延性を
低下させることから、M含有量の上限は2%と定めた。Ap has an important function of causing transformation-induced plasticity (TRIP) to appear by suppressing the precipitation of the ω phase that inhibits deformation-induced martensitic transformation. However, if the M content exceeds 2%, the shear resistance during martensitic transformation increases, and conversely, deformation-induced martensitic transformation is suppressed and ductility decreases, so the upper limit of the M content was set at 2%.
なお、単独添加の場合には1%以上の添加量を確保する
のが好ましい。In addition, in the case of single addition, it is preferable to ensure an addition amount of 1% or more.
と
SnにもAlと同様の作用があるが、Snの場合には6
%を越えて添加すると八!におけると同じ不都合を生じ
て延性を低下するようになることから、Sn含有量の上
限は6%と定めた。なお、Snを単独で添加する場合に
は4%以上の添加量を確保するのが好ましい。and Sn have the same effect as Al, but in the case of Sn, 6
If you add more than 8%! The upper limit of the Sn content was set at 6% because the same disadvantages as in the above occur and the ductility decreases. In addition, when Sn is added alone, it is preferable to ensure an addition amount of 4% or more.
如
ZrもANと同様の作用を有しているが、そのω相析出
抑制効果はAlやSnはど大きくはない。そのため、特
に八βやSnとの複合添加が推奨される成分である。そ
して、ApやSnとの複合添加を行うと、加工誘起マル
テンサイト量を適度に調整して合金の延性を効率良く高
める効果を発揮する。しかし、6%を越えて含有させる
と、八βやSnの場合と同じ不都合を生じて延性を低下
するようになることから、Zr含有量の上限は6%と定
めた。なお、Zrを添加する場合も、できれば4%以上
の添加量を確保するのが望ましい。Zr also has the same effect as AN, but its ω phase precipitation suppressing effect is not as great as that of Al and Sn. Therefore, it is particularly recommended to add it in combination with octaβ and Sn. When Ap and Sn are added in combination, the amount of deformation-induced martensite is adjusted appropriately and the ductility of the alloy is effectively increased. However, if the Zr content exceeds 6%, the same problems as those of 8β and Sn will occur and the ductility will decrease, so the upper limit of the Zr content was set at 6%. Note that even when Zr is added, it is desirable to ensure an addition amount of 4% or more if possible.
〈作用〉
本発明のチタン合金は上述のように構成されるものであ
るが、このチタン合金が極めて優れた延性を示すのは次
の理由によるものと考えられる。<Function> The titanium alloy of the present invention is constructed as described above, and the reason why this titanium alloy exhibits extremely excellent ductility is considered to be due to the following reason.
即ち、先にも述べたように、適正量の■を含有させてβ
相を準安定な状態とし、かつ適量のsn、 AI!+Z
rの1種又は2種以上を添加して構成されたβ型チタン
合金は、塑性変形を行うと、β相が準安定状態であるこ
ととSn、 AI!、 Zrが有するω相析出抑 。That is, as mentioned earlier, by containing an appropriate amount of
The phase is made metastable, and an appropriate amount of sn, AI! +Z
When a β-type titanium alloy made by adding one or more types of r is plastically deformed, the β phase is in a metastable state and Sn, AI! , Suppression of ω phase precipitation possessed by Zr.
制作用とによって塑性変形中にマルテンサイト変態を伴
う変態誘起塑性(TRIP)を発揮することとなる。そ
のため、常温にて該チタン合金製板材のプレス成形加工
が可能となる程に合金の延性が改善されるものである。Depending on the production use, it exhibits transformation-induced plasticity (TRIP) accompanied by martensitic transformation during plastic deformation. Therefore, the ductility of the alloy is improved to such an extent that the titanium alloy plate material can be press-formed at room temperature.
続いて、この発明を実施例により比較例と対比しながら
具体的に説明する。Next, the present invention will be specifically explained using examples and comparing with comparative examples.
〈実施例〉
第1表に示されるような各種成分組成のチタン合金をア
ルゴンアーク溶解によって溶製し、得られた鋳塊を熱延
及び冷延してIB厚の板材を製造した。<Example> Titanium alloys having various compositions as shown in Table 1 were melted by argon arc melting, and the obtained ingots were hot-rolled and cold-rolled to produce plates of IB thickness.
次いで、これら各チタン板に溶体化処理を施しから引張
試験片を切り出し、常温での引張試験によって機械的性
質を測定した。Next, each of these titanium plates was subjected to solution treatment, and tensile test pieces were cut out, and mechanical properties were measured by a tensile test at room temperature.
これらの試験結果も第1表に併せて示した。These test results are also shown in Table 1.
第1表の結果からも明らかなように、本発明に係るチタ
ン合金は極めて優れた伸び値を示し、常温でのプレス成
形加工が可能であることが分かる。As is clear from the results in Table 1, the titanium alloy according to the present invention exhibits an extremely excellent elongation value and can be press-formed at room temperature.
〈効果の総括〉
以上に示した如く、この発明によれば、優れた延性を安
定して示し、常温での板材のプレス成形加工も可能なチ
タン合金を提供できるなど、産業上極めて有用な効果が
もたらされるのである。<Summary of Effects> As described above, the present invention has extremely useful effects industrially, such as being able to provide a titanium alloy that stably exhibits excellent ductility and can be press-formed into plate materials at room temperature. is brought about.
出願人 日本ステンレス株式会社Applicant: Nippon Stainless Co., Ltd.
Claims (1)
更に Al:2%以下、 Zr:6%以下、 Sn:6%以下 のうちの1種以上をも含み、残部が実質的にTiから成
ることを特徴とする、延性に優れたチタン合金。[Claims] Contains 16 to 2.0% V by weight, and
A titanium alloy with excellent ductility, which further contains one or more of the following: Al: 2% or less, Zr: 6% or less, and Sn: 6% or less, with the remainder substantially consisting of Ti.
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP770088A JPH01184242A (en) | 1988-01-18 | 1988-01-18 | Titanium alloy having excellent ductility |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP770088A JPH01184242A (en) | 1988-01-18 | 1988-01-18 | Titanium alloy having excellent ductility |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| JPH01184242A true JPH01184242A (en) | 1989-07-21 |
Family
ID=11673040
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP770088A Pending JPH01184242A (en) | 1988-01-18 | 1988-01-18 | Titanium alloy having excellent ductility |
Country Status (1)
| Country | Link |
|---|---|
| JP (1) | JPH01184242A (en) |
Cited By (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JPH02129331A (en) * | 1988-11-09 | 1990-05-17 | Sumitomo Metal Ind Ltd | Beta-type titanium alloy having excellent cold workability |
| JP2007327132A (en) * | 2006-06-09 | 2007-12-20 | Kobe Steel Ltd | Titanium alloy with excellent press formability, and press formed member |
-
1988
- 1988-01-18 JP JP770088A patent/JPH01184242A/en active Pending
Cited By (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JPH02129331A (en) * | 1988-11-09 | 1990-05-17 | Sumitomo Metal Ind Ltd | Beta-type titanium alloy having excellent cold workability |
| JP2007327132A (en) * | 2006-06-09 | 2007-12-20 | Kobe Steel Ltd | Titanium alloy with excellent press formability, and press formed member |
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