JPH03243740A - Titanium alloy excellent in superplastic workability and its manufacture as well as method for superplastic working of titanium alloy - Google Patents
Titanium alloy excellent in superplastic workability and its manufacture as well as method for superplastic working of titanium alloyInfo
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- superplastic
- titanium alloy
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Abstract
(57)【要約】本公報は電子出願前の出願データであるた
め要約のデータは記録されません。(57) [Summary] This bulletin contains application data before electronic filing, so abstract data is not recorded.
Description
【発明の詳細な説明】
[産業上の利用分野]
この発明は、高強度の超塑性加工性に優れたチタン合金
、及びその製造方法に関する。DETAILED DESCRIPTION OF THE INVENTION [Field of Industrial Application] The present invention relates to a titanium alloy with high strength and excellent superplastic workability, and a method for producing the same.
[従来の技術]
チタン合金は、軽量でかつ強靭なことから、近時、飛行
機、ロケット等の航空宇宙機器用材料として盛んに用い
られつつある。しかしながら、チタン合金は難加工性材
料であり、複雑形状部材を製造する場合には製品歩留り
が著しく低く、製造コストが著しく高くなってしまうと
いう問題点がある。[Prior Art] Titanium alloys are lightweight and strong, and have recently been increasingly used as materials for aerospace equipment such as airplanes and rockets. However, titanium alloy is a material that is difficult to process, and when manufacturing a member with a complex shape, there are problems in that the product yield is extremely low and the manufacturing cost is extremely high.
このような問題点を解消するために有効な加工法として
超塑性加工が知られている。超塑性加工は超塑性現象を
利用した加工方法であり、特に微細結晶粒で見られる微
細粒超塑性を利用したものが工業的に重要である。チタ
ン合金の中で最も広く用いられているT 1−6Ai)
−4V合金においても、5〜10μmの微細粒組織を有
した材料は超塑性加工が行われているが、その加工温度
は875乃至950℃と高く、加工治具の寿命が短い、
治具として高温強度を有する高価な材料を用いざるを臀
ない等、設備上及び操業上の多くの問題点を含んでいる
。Superplastic processing is known as an effective processing method for solving these problems. Superplastic processing is a processing method that utilizes superplastic phenomena, and in particular, methods that utilize fine grain superplasticity observed in fine crystal grains are industrially important. T1-6Ai) is the most widely used titanium alloy.
Even in -4V alloy, materials with fine grain structures of 5 to 10 μm are subjected to superplastic processing, but the processing temperature is as high as 875 to 950°C, and the life of the processing jig is short.
This involves many problems in terms of equipment and operation, such as the necessity of using expensive materials with high-temperature strength as the jig.
そこで、T 1−6Aj7−4V合金以上に優れた超塑
性特性をaすること、及び、超塑性加工温度を下げるこ
とを目的として、T 1−6Ap −4V合金にFe、
Co、又はFe、Co、Niを添加した合金が開発され
ている(米国特許4.299,626号)。Therefore, with the aim of achieving superior superplastic properties than the T 1-6Aj7-4V alloy and lowering the superplastic processing temperature, we added Fe to the T 1-6Ap-4V alloy.
Co, or alloys to which Fe, Co, and Ni are added have been developed (US Pat. No. 4,299,626).
[発明が解決しようとする課題]
しかしながら、このようなT 1−6AN −4V−F
e−Co−Ni合金においても、超塑性加工温度がT
i −6A(1−4Vよりも50乃至80℃a、t i
’ しているにすぎず、未だ充分とはいえない。[Problem to be solved by the invention] However, such T 1-6AN-4V-F
Also in the e-Co-Ni alloy, the superplastic working temperature is T
i -6A (50~80℃a than 1-4V, t i
' However, it is still not enough.
また、超塑性伸びも充分でない。Further, superplastic elongation is also insufficient.
一方、たとえ超塑性加工温度を十分に低下させることが
できたとしても、超塑性加工時の変形抵抗が大きければ
加工が困難になってしまう。On the other hand, even if the superplastic working temperature can be lowered sufficiently, if the deformation resistance during superplastic working is large, the working will become difficult.
この発明はかかる事情に鑑みてなされたものであって、
超塑性加工温度が低く、超塑性加工時の変形抵抗が小さ
く、従来のチタン合金よりも超塑性延びが大きい超塑性
加工性に優れたチタン合金及びその製造方法、並びにこ
のようなチタン合金の超塑性加工方法を提供することを
目的とする。This invention was made in view of such circumstances, and
A titanium alloy with excellent superplastic workability that has a low superplastic working temperature, low deformation resistance during superplastic working, and greater superplastic elongation than conventional titanium alloys, and a method for producing the same, as well as a method for producing such a titanium alloy. The purpose is to provide a plastic working method.
[課題を解決するための手段及び作用コこの発明に係る
超塑性加工性に優れたチタン合金は、重量%で、Ail
:6.5〜6675%、V:3.5〜4.5%、O:0
.2%以下、Cr:0.85〜3.15%、Mo :
0.85〜3.15%を含有し、かつ、
3%≦f1.8x (Cr%)+(Mo%)}≦8%
の条件を満足し、残部がTi及び不可避不純物からなり
、α晶の半均粒径が6μm以下であることを特徴とする
。[Means and effects for solving the problem] The titanium alloy having excellent superplastic workability according to the present invention has Ail
: 6.5-6675%, V: 3.5-4.5%, O: 0
.. 2% or less, Cr: 0.85-3.15%, Mo:
It contains 0.85 to 3.15% and satisfies the following conditions: 3%≦f1.8x (Cr%)+(Mo%)}≦8%, the remainder consists of Ti and inevitable impurities, and the α crystal It is characterized by having a semi-average particle size of 6 μm or less.
この発明に係る超塑性加工性に優れたチタン合金の製造
方法は、重量%で、AI! : 6.5〜6.75%、
V:3,5〜4.5%、O:0.2%以下、Cr:0.
85〜3.15%、MO:0.85〜3,15%、を含
有し、かつ、3%≦f1.8x (Cr%) +(Mo
%)}≦8%
の条件を満足し、残部がTi及び不可避不純物からなる
チタン合金を、(β変態点−200℃)以上、β変態点
未満の温度で加熱し、引き続き、β変態点未満の温度で
圧下比を3以上とする圧下を施すことを特徴とする。The method for producing a titanium alloy with excellent superplastic workability according to the present invention is based on the weight percentage of AI! : 6.5-6.75%,
V: 3.5-4.5%, O: 0.2% or less, Cr: 0.
85 to 3.15%, MO: 0.85 to 3.15%, and 3%≦f1.8x (Cr%) + (Mo
%)}≦8%, and the remainder consists of Ti and unavoidable impurities, is heated at a temperature above (β transformation point -200°C) and below the β transformation point, and then heated to a temperature below the β transformation point. It is characterized by applying rolling at a rolling ratio of 3 or more at a temperature of .
この発明に係るチタン合金の超塑性加工方法は、重量%
で、A1Al: 6.5〜6.75%、V:3,5〜4
.5%、O:0.2%以下、Cr:0. 85〜3.
15%、Mo:0.85〜3.15%を含有し、かつ、
3%≦(1,8X (Cr%) +(Mo%))58%
の条件を満足し、残部がTi及び不可避不純物からなる
チタン合金を、(β変態点−200”C)以上、β変態
点未満の温度で加熱し、引き続き、β変態点未満の温度
で圧下比を3以上とする圧下を施し、(β変態点−20
0℃)以上、β変態点未満の温度で再結晶熱処理を施し
、超塑性加工を施すことを特徴とする。The method for superplastic processing of titanium alloy according to this invention includes
So, A1Al: 6.5-6.75%, V: 3.5-4
.. 5%, O: 0.2% or less, Cr: 0. 85-3.
15%, Mo: 0.85 to 3.15%, and satisfies the condition of 3%≦(1,8X (Cr%) + (Mo%))58%, with the remainder being Ti and unavoidable impurities. A titanium alloy made of Points -20
It is characterized by performing recrystallization heat treatment at a temperature of 0° C. or higher and lower than the β transformation point, and performing superplastic working.
本願発明者らは、上述のような特性を有するチタン合金
を開発すべく以下に示す観点から種々検討した結果、上
記構成を有する本発明を完成させるに至った。The inventors of the present application conducted various studies from the following viewpoints in order to develop a titanium alloy having the above characteristics, and as a result, they completed the present invention having the above structure.
高強度であり、かつ超塑性加工が可能であるチタン合金
を得るためには、そのミクロ組織を微細な等軸0品を有
する組織にしなければならない。In order to obtain a titanium alloy that has high strength and is capable of being superplastically worked, its microstructure must have fine equiaxed elements.
また、チタン合金の超塑性現象が発現するためには、そ
のミクロ組織において、α相の体積率が40〜60%で
あることが必要である。従って、Ti−6Ajl −4
V合金よりも超塑性加工温度を低下させるためには、β
変態点を低下させる元素、すなわちC「、Moを添加す
ればよい。Further, in order for the titanium alloy to exhibit the superplastic phenomenon, it is necessary that the volume fraction of the α phase be 40 to 60% in its microstructure. Therefore, Ti-6Ajl -4
In order to lower the superplastic processing temperature than V alloy, β
Elements that lower the transformation point, ie, C and Mo, may be added.
しかし、Crは強度゛上昇に大きく寄与するものの、こ
れらの含有量が多すぎると、Tiとの間に脆化相である
金属間化合物を形成したり、溶解時にβフレックと称さ
れる偏析相を生威し、その結果機械的性質を劣化させる
ため好ましくない。However, although Cr greatly contributes to an increase in strength, if its content is too high, it may form intermetallic compounds, which are brittle phases, with Ti, or a segregated phase called β flake may occur during melting. This is undesirable because it causes the mechanical properties to deteriorate as a result.
Moも同様に強度上昇に寄与するが、添加量が多すぎる
と、チタン合金の比重を増大させ、高比強度材料である
チタン合金の特色を損なうと共に、β相ψでの拡散速度
が小さい元素であるため、超塑性加工時の変形抵抗を増
大させ、好ましくない。Mo also contributes to an increase in strength, but if it is added in too large an amount, it increases the specific gravity of the titanium alloy, impairing the characteristics of the titanium alloy as a material with high specific strength, and is an element that has a low diffusion rate in the β phase ψ. Therefore, it increases the deformation resistance during superplastic processing, which is undesirable.
従って、これらの含有量をこれら不都合が生じない一定
範囲に規定する必要がある。Therefore, it is necessary to define their content within a certain range that does not cause these inconveniences.
これらの元素によるチタン合金のβ相安定度は、1、
8x (Cr%)+(Mo%)で示され、この値が小さ
いとβ変態点が高く、逆に大きいとβ変態点が低くなる
。チタン合金の最適超塑性温度、すなわち超塑性現象が
発現し得る温度は、上述したようにα相の体積率が40
〜60%になる温度であり、この温度はβ変態点と密接
な関係がある。The β phase stability of titanium alloys with these elements is 1,
It is expressed as 8x (Cr%)+(Mo%), and when this value is small, the β-transformation point is high, and conversely, when this value is large, the β-transformation point is low. As mentioned above, the optimum superplastic temperature of a titanium alloy, that is, the temperature at which superplastic phenomena can occur, is when the volume fraction of the α phase is 40.
~60%, and this temperature is closely related to the β transformation point.
すなわち、この値が小さ過ぎると超塑性発現温度が低い
という利点を得ることができず、大き過ぎるとα相の体
積率が40〜60%になる温度が低くなり過ぎ、その温
度では原子拡散が不十分となり、十分な超塑性伸びが得
られない。従って、優れた超塑性加工性を得るためには
、この値を適切な範囲に規定する必要がある。In other words, if this value is too small, the advantage of a low superplasticity onset temperature cannot be obtained, and if it is too large, the temperature at which the volume fraction of the α phase is 40 to 60% will be too low, and atomic diffusion will not occur at that temperature. This results in insufficient superplastic elongation. Therefore, in order to obtain excellent superplastic workability, it is necessary to define this value within an appropriate range.
また、微細粒超塑性特性はその結晶粒径に大きく依存し
、粒径が小さい程良好な特性を得ることができる。従っ
て、結晶粒径の上限を超塑性特性を損なわない程度に規
定する必要がある。このような結晶粒の微細化は、最終
熱間加工を、その後の再結晶熱処理により等軸α晶の微
細再結晶組織が得られるような条件で施すことにより達
成される。すなわち、最終熱間加工条件が適切でなけれ
ば、その後の再結晶熱処理によって等軸0品の微細再結
晶組織を得ることができない。Further, the fine grain superplastic properties largely depend on the crystal grain size, and the smaller the grain size, the better the properties can be obtained. Therefore, it is necessary to define the upper limit of the crystal grain size to an extent that does not impair the superplastic properties. Such grain refinement is achieved by performing the final hot working under conditions such that a fine recrystallized structure of equiaxed α crystals can be obtained by the subsequent recrystallization heat treatment. That is, unless the final hot working conditions are appropriate, a fine recrystallized structure with zero equiaxes cannot be obtained by the subsequent recrystallization heat treatment.
更に、最終熱間圧延後の再結晶熱処理は、超塑性加工を
行う上での前提であり、この処理を適切に行うことによ
り、その後の超塑性加工を良好に行うことができる。Furthermore, the recrystallization heat treatment after the final hot rolling is a prerequisite for performing superplastic working, and by appropriately performing this treatment, the subsequent superplastic working can be performed satisfactorily.
次に、本発明においてこの発明に係るチタン合金の各成
分を上記範囲に限定した理由について説明する。Next, the reason why each component of the titanium alloy according to the present invention is limited to the above range in the present invention will be explained.
All:A1はα+β組織を得るためのα相安定化元素
として添加され、強度上昇に寄与する。All:A1 is added as an α-phase stabilizing element to obtain an α+β structure, and contributes to an increase in strength.
しかし、その含有量が6.5%未満では、目的とする強
度を得るのに不十分である。また、含有量が6.75%
を超えると、脆化相であるα、相(T i ) Al2
)が析出し、機械的性質を劣化させるため好ましくな
い。従って1.I’1ffiを5,5〜6.75%の範
囲に規定する。However, if the content is less than 6.5%, it is insufficient to obtain the desired strength. In addition, the content is 6.75%
, the brittle phase α, phase (T i ) Al2
) is undesirable because it precipitates and deteriorates mechanical properties. Therefore 1. I'1ffi is defined in the range of 5.5 to 6.75%.
■: vはα+β組織を得るためのβ相安定化元素とし
て添加され、Tiとの間に脆化相である金属間化合物を
形成することなく強度上昇に寄与する。しかし、含有量
が3.5%未満では目的とする強度を得るのに不十分で
あり、また、含有量が4.5%を超えると超塑性伸びを
低減させると供に超塑性加工時の変形抵抗を増大させる
。従って、v量を3.5〜4.5%に規定した。(2): v is added as a β phase stabilizing element to obtain an α+β structure, and contributes to an increase in strength without forming an intermetallic compound, which is a brittle phase, with Ti. However, if the content is less than 3.5%, it is insufficient to obtain the desired strength, and if the content exceeds 4.5%, it will reduce the superplastic elongation and Increases deformation resistance. Therefore, the v amount was defined as 3.5 to 4.5%.
O: 0はα相に固溶して強度上昇に寄与する。O: 0 is dissolved in the α phase and contributes to an increase in strength.
しかし、その含有量が0.2%を超えるとβ変態点を上
Hさせ、また、室温での機械的性質、特に延性を劣化さ
せる。従って、OHiを0.2%以下に規定する。However, if its content exceeds 0.2%, it will raise the β-transus point and deteriorate mechanical properties, especially ductility, at room temperature. Therefore, OHi is defined to be 0.2% or less.
Cr: Crはβ相安定化元素として添加され、β変
態点を低下させることにより超塑性特性の向上(超塑性
伸びの増大及び変形抵抗の低減)に寄与すると共に、主
にβ相に固溶し、室温の強度上昇に寄与する。しかし、
その含有量が0.85%未満ではこれら超塑性特性の向
上及び室温強度上昇への寄与が不十分である。また、3
.15%を超えるとTiとの間に脆化相である金属間化
合物を形成したり溶解時にβフレックを生成し、その結
果延性を劣化させてしまう。従って、Crff1を0.
85〜3.15%の範囲に規定する。Cr: Cr is added as a β-phase stabilizing element, and contributes to improving superplastic properties (increasing superplastic elongation and reducing deformation resistance) by lowering the β-transformation point, and is mainly formed as a solid solution in the β-phase. This contributes to an increase in strength at room temperature. but,
If its content is less than 0.85%, its contribution to improving these superplastic properties and increasing room temperature strength is insufficient. Also, 3
.. If it exceeds 15%, an intermetallic compound, which is a brittle phase, is formed with Ti, or β flakes are generated during melting, resulting in deterioration of ductility. Therefore, Crff1 is set to 0.
It is defined in the range of 85 to 3.15%.
Mo:Moもβ相安定化元素として添加され、β変態点
を低下させることにより超塑性特性の向上(超塑性発現
温度の低下)に寄与すると共に、主にβ相に固溶して強
度上昇に寄与する。しかし、含有量が0.85%未満で
はこれら効果が不十分である。また、3.15%を超え
ると、MOが重い金属であることから合金の密度を増大
させ、高比強度であるというチタン合金の特徴を損なう
と共に、MOはチタン中での拡散速度が小さいために超
塑性成形時の変形応力を増大させてしまう。Mo: Mo is also added as a β-phase stabilizing element, which contributes to improving superplastic properties (lowering the superplasticity onset temperature) by lowering the β-transformation point, and increases strength by mainly dissolving in the β-phase. Contribute to However, if the content is less than 0.85%, these effects are insufficient. Moreover, if it exceeds 3.15%, MO is a heavy metal, which increases the density of the alloy, impairing the high specific strength of titanium alloy, and also because MO has a low diffusion rate in titanium. This increases the deformation stress during superplastic forming.
従って、MO量を0.85〜3.15%の範囲に規定す
る。Therefore, the amount of MO is defined in the range of 0.85 to 3.15%.
1.8X (Cr%)+(Mo%)は、チタン合金のβ
相安定度を示し、前述したように、これらの値が小さい
とβ変態点が高く、逆に大きいとβ変態点が低くなる。1.8X (Cr%) + (Mo%) is β of titanium alloy
It indicates phase stability, and as mentioned above, when these values are small, the β-transformation point is high, and conversely, when these values are large, the β-transformation point is low.
チタン合金の最適超塑性温度、すなわち超塑性現象が発
現し得る温度は、上述したようにα相の体積率が40〜
60%になる温度であり、この温度はβ変態点と密接な
関係がある。As mentioned above, the optimal superplastic temperature of a titanium alloy, that is, the temperature at which superplastic phenomena can occur, is when the volume fraction of the α phase is 40 to 40.
60%, and this temperature is closely related to the β transformation point.
この値が3%未満であると超塑性発現温度が低いという
本発明の特徴を損ない、また、8%を超えるとα相の体
積率が40〜60%になる温度が低くなり過ぎ、その温
度では原子拡散が不十分となり、十分な超塑性伸びが得
られない。If this value is less than 3%, the characteristic of the present invention that the superplasticity development temperature is low will be impaired, and if it exceeds 8%, the temperature at which the volume fraction of the α phase becomes 40 to 60% will be too low, and the temperature In this case, atomic diffusion becomes insufficient and sufficient superplastic elongation cannot be obtained.
従って、この値を、3%≦f1.8X (Cr%)+(
Mo%)}≦8%に規定する。Therefore, this value is 3%≦f1.8X (Cr%)+(
Mo%)}≦8%.
次に、α晶粒径の限定理由について説明する。Next, the reason for limiting the α crystal grain size will be explained.
α晶粒径は超塑性特性と密接な関係があり、これが小さ
い捏上れた超塑性特性を示す。この発明に係るチタン合
金においては、α晶の平均粒径が6μmを超えると超塑
性伸びが小さくなるばかりでなく、変形応力が大きくな
り好ましくない。従って、0品粒径を6μm以下に規定
する。The α grain size has a close relationship with superplastic properties, and this shows small rolled up superplastic properties. In the titanium alloy according to the present invention, if the average grain size of the α-crystal exceeds 6 μm, not only the superplastic elongation decreases but also the deformation stress increases, which is not preferable. Therefore, the zero-product particle size is defined as 6 μm or less.
0品粒径を6μ以下にするためには以下に示す方法が採
用される。In order to reduce the zero particle size to 6 μm or less, the following method is adopted.
先ず、熱間鍛造、又は熱間圧延、又はこの両方により、
チタン合金インゴットを加工製造してスラブとし、次い
で、このスラブを再加熱して熱間加工を施し最終4広と
する。最終熱間加工においては、以下の3つの条件を満
足させる必要がある。First, by hot forging, hot rolling, or both,
A titanium alloy ingot is processed and produced into a slab, and then this slab is reheated and hot worked to form a final 4-piece. In the final hot working, it is necessary to satisfy the following three conditions.
■その加熱温度を(β変態温度−200℃)以上、β変
態点未満とする。■加工中に被加工材の温度がβ変態点
以上にならないようにする。■加工の際の圧下比を3以
上とする。(2) The heating temperature is set to be at least (β-transformation temperature - 200°C) and below the β-transformation point. ■Prevent the temperature of the workpiece from rising above the β transformation point during processing. ■The rolling reduction ratio during processing should be 3 or more.
このように条件を規定した理由は以下の通りである。The reason for defining the conditions in this way is as follows.
■については、加熱温度がβ変態点以上であると、加工
後に再結晶焼鈍を行っても、超塑性成形に適した等軸組
織ではなく、棒状のα晶組織となり、しかも旧β粒界に
α晶が生威し、超塑性特性及び室温での延性を劣化させ
る。また、加熱温度がβ変態点−200℃未満であると
、温度が低すぎて加工中に割れ等の結果が発生する。Regarding (2), if the heating temperature is above the β transformation point, even if recrystallization annealing is performed after processing, a rod-shaped α crystal structure will be formed instead of an equiaxed structure suitable for superplastic forming, and furthermore, the former β grain boundaries will be α crystals grow and deteriorate superplastic properties and ductility at room temperature. Further, if the heating temperature is lower than the β-transus point -200°C, the temperature is too low and results such as cracking occur during processing.
■については、加工中に被加工物の温度がβ変態点以上
になると、■と同様棒状のα組織となってしまう。As for (2), when the temperature of the workpiece becomes higher than the β transformation point during processing, it becomes a rod-shaped α structure as in (2).
■については、圧下比が3未満と小さいと、α晶に再結
晶に十分な歪みが蓄えられず、再結晶熱処理を行っても
、超塑性成形に適した微細粒等軸組織ではなく、棒状の
α晶組織や粗大なα組織となり好ましくない。Regarding (2), if the reduction ratio is small (less than 3), sufficient strain for recrystallization will not be stored in the α-crystals, and even if recrystallization heat treatment is performed, the microstructure will not form a fine-grained equiaxed structure suitable for superplastic forming, but will have a rod-like structure. This results in an α crystal structure or a coarse α structure, which is undesirable.
次に、超咽性加工に先立って行われる再結晶熱処理条件
の限定理由について説明する。Next, the reasons for limiting the recrystallization heat treatment conditions performed prior to superpharyngeal processing will be explained.
再結晶熱処理が(β変態点−200℃)未満では、温度
が低すぎて再結晶が十分に行われないため等軸位が得ら
れず好ましくない。また、熱処理温度がβ変態点以上に
なると、等軸0品が消失してβ単相となり、超塑性が得
られないので好ましくない。従って、再結晶熱処理温度
を(β変態点200℃)以上、β変態点未満と規定した
。If the recrystallization heat treatment is less than (β-transus point −200° C.), the temperature is too low and recrystallization is not performed sufficiently, so that equiaxed orientation cannot be obtained, which is not preferable. Furthermore, if the heat treatment temperature exceeds the β transformation point, the zero equiaxed product disappears and becomes a β single phase, which is not preferable because superplasticity cannot be obtained. Therefore, the recrystallization heat treatment temperature was specified to be higher than (β transformation point 200° C.) and lower than β transformation point.
なお、超塑性加工は、再結晶熱処理に引き続いて行って
もよいし、再結晶熱処理と同時に行ってもよい。Note that the superplastic working may be performed subsequent to the recrystallization heat treatment, or may be performed simultaneously with the recrystallization heat treatment.
[実施例] 以下、この発明の実施例について詳細に説明する。[Example] Examples of the present invention will be described in detail below.
第1表に示す組成を有する合金について、アルゴン雰囲
気のアーク炉にてインゴットを溶製し、熱間鍛巡により
各極厚みのスラブを製造した。Ingots of alloys having the compositions shown in Table 1 were melted in an arc furnace in an argon atmosphere, and slabs of various thicknesses were produced by hot forging.
次いで、これらのスラブを夫々第1表に示す温度に再加
熱し、引続き、これらスラブに対し夫々第1表に示す圧
下比で圧延加工を施して厚さ5■膳の板材に仕上げた。Next, each of these slabs was reheated to the temperature shown in Table 1, and subsequently, each of these slabs was rolled at the rolling reduction ratio shown in Table 1, respectively, to form a plate material having a thickness of 5 mm.
そして、このようにして仕上げた板材に対し再結晶熱処
理を施した。この再結晶熱処理は、実験番号C15以外
は、(β変態点−200℃)以上、β変態点未満の温度
域で行った。この再結晶熱処理に引き続いて超塑性引張
試験を行った。また、再結晶熱処理を施した各板材につ
いてα品粒径(平均粒径)の測定、及び室温引張試験を
合わせて行った。α結晶粒の測定は線分法により行い、
アスペクト比(長袖と短軸との比)が3以上の棒状組織
のものについては粒径の測定を行わなかった。The plate material thus finished was then subjected to recrystallization heat treatment. This recrystallization heat treatment was performed in a temperature range of (β transformation point −200° C.) or higher and lower than the β transformation point, except for experiment number C15. Following this recrystallization heat treatment, a superplastic tensile test was conducted. In addition, for each sheet material subjected to recrystallization heat treatment, the α grain size (average grain size) was measured and a room temperature tensile test was performed. α grains are measured by the line segment method.
The particle size was not measured for rod-like structures with an aspect ratio (ratio of long sleeve to short axis) of 3 or more.
各板材の再結晶熱処理の温度及びα結晶粒径を合わせて
第1表に示し、室温引張試験及び超塑性引張試験の結果
を第2表に示す。Table 1 shows the recrystallization heat treatment temperature and α grain size of each plate, and Table 2 shows the results of the room temperature tensile test and superplastic tensile test.
なお、第1表中、実験番号A1〜A7は本発明の範囲内
である実施例を示し、81〜B4は従来例(従来例中(
1)はT L−6A# −4V合金、(2) はTi−
6AI! −4V−Co−(Ni)合金)、C1〜C1
5は本発明の範囲から外れる比較例である。また、各実
験番号の組成におけるβ変態点も合わせて第1表に記し
た。In Table 1, experiment numbers A1 to A7 indicate examples within the scope of the present invention, and 81 to B4 indicate conventional examples (in the conventional examples (
1) is T L-6A#-4V alloy, (2) is Ti-
6AI! -4V-Co-(Ni) alloy), C1~C1
No. 5 is a comparative example outside the scope of the present invention. In addition, the β transformation points for the compositions of each experiment number are also listed in Table 1.
なお、超塑性引張試験は、平行部が5■幅、5同長さ、
4mm厚さの試験片を用いて、5X10−6Torr以
下の真空ψで行った。また、最大変形応力は、最大加重
を初期断面積で除して求めた。In addition, in the superplastic tensile test, the parallel part is 5 cm wide, 5 cm long,
The test was carried out using a test piece with a thickness of 4 mm at a vacuum ψ of 5×10 −6 Torr or less. Further, the maximum deformation stress was determined by dividing the maximum load by the initial cross-sectional area.
これら第1表及び第2表に示すように、実施例である実
験番号A1〜A7は、合金組成が本発明の範囲内であり
、しかも、製造条件が本発明に係る方法に沿っているた
め、0品粒径が極めて微細であり、6μm以下を十分に
満足している。また、室温引張特性においても引張強さ
が105 kgf / m1以上で、伸びが17%以上
であり、T i−6/’1−4V合金よりも良好な値を
示すことが確認された。As shown in Tables 1 and 2, the experimental numbers A1 to A7, which are examples, have alloy compositions within the scope of the present invention, and the manufacturing conditions are in accordance with the method according to the present invention. The particle size of the 0 product is extremely fine and fully satisfies the requirement of 6 μm or less. Furthermore, it was confirmed that the tensile strength at room temperature was 105 kgf/m1 or more, and the elongation was 17% or more, which were better values than the Ti-6/'1-4V alloy.
次に、第2表に示す超塑性引張特性について、第1図乃
至第6図を参照しながら説明する。Next, the superplastic tensile properties shown in Table 2 will be explained with reference to FIGS. 1 to 6.
第1図は、1.8X (Cr%)+(Mo%)の値と超
塑性伸びとの関係を示すグラフである。この図から明ら
かなように、この値が本発明の範囲内である3〜8%の
範囲で1500%以上の大きな伸びが得られることが確
認された。FIG. 1 is a graph showing the relationship between the value of 1.8X (Cr%)+(Mo%) and superplastic elongation. As is clear from this figure, it was confirmed that a large elongation of 1500% or more can be obtained when this value is within the range of 3 to 8%, which is within the range of the present invention.
第2図は、Crの含有量と超塑性伸びとの関係を示すグ
ラフである。この図から明らかなように、この値が本発
明の範囲内である0、85〜3.15%の範囲で150
0%以上の大きな伸びかられることが確認された。FIG. 2 is a graph showing the relationship between Cr content and superplastic elongation. As is clear from this figure, this value is within the range of the present invention, 150% in the range of 0.85% to 3.15%.
It was confirmed that there was a large elongation of 0% or more.
第3図は、Moの含有量と超塑性伸びとの関係を示すグ
ラフである。この図から明らかなように、この値が本発
明の範囲内である0、85〜3.15%の範囲で150
0%以上の大きな伸びかられることが確認された。FIG. 3 is a graph showing the relationship between Mo content and superplastic elongation. As is clear from this figure, this value is within the range of the present invention, 150% in the range of 0.85% to 3.15%.
It was confirmed that there was a large elongation of 0% or more.
第4図は、0品粒径と超塑性伸びとの関係を示すグラフ
である。この図から明らかなように、この値が本発明の
範囲内である6μm以下であれば1500%以上の大き
な伸びかられることが確認された。FIG. 4 is a graph showing the relationship between 0-product grain size and superplastic elongation. As is clear from this figure, it was confirmed that a large elongation of 1500% or more can be achieved if this value is 6 μm or less, which is within the range of the present invention.
以上のように、本発明で規定された組成範囲及び粒径範
囲で優れた超塑性特性が得られることが確認された。As described above, it was confirmed that excellent superplastic properties can be obtained within the composition range and particle size range specified in the present invention.
本発明の範囲内である試験番号A1〜A7は上述のよう
に超塑性伸びが1500%以上と良好であるのみならず
、最大超塑性伸びを示す温度が800℃以下とT 1−
6Afl −4V合金よりも75〜100℃も低く、更
にその温度が極めて低いのにもかかわらず、その温度に
おける変形応力が1 、41 kg「/s+ga2以下
と小さいことが確認された。Test numbers A1 to A7, which are within the scope of the present invention, not only have a good superplastic elongation of 1500% or more as described above, but also have a temperature of 800°C or less at which the maximum superplastic elongation occurs, which is T1-
It was confirmed that the deformation stress at that temperature was as small as 1.41 kg/s+ga2 or less, even though the temperature was 75 to 100°C lower than that of the 6Afl-4V alloy and was extremely low.
これに対し、比較例であるC1〜C14では超塑性伸び
の値が実施例よりも低いことが確認された。On the other hand, it was confirmed that the superplastic elongation values of Comparative Examples C1 to C14 were lower than those of the Examples.
比較例の中でC1〜CIOは組成が本発明の範囲から外
れるものであり、これらのうちC3、C5、及びC9は
1320%以上と比較的大きな伸びを示すが、最大超塑
性伸びが得られた温度が825℃以上と実施例のものよ
りも25〜50’C高く、超塑性特性が実施例のものよ
りも明らかに劣っていることが確認された。C7、cl
oは最大超塑性伸びが得られた温度が750’Cと極め
て低いが、超塑性伸びが夫々1300%、780%に止
まり、また変形応力が夫々2.85kgr / *m’
2 、 80 kgl’ / g+v’と極めて大
きい値となツタ。C1、C2、C4、C6においても、
超塑性伸びが1000%前後と不十分であった。Among the comparative examples, C1 to CIO have compositions outside the scope of the present invention, and among these, C3, C5, and C9 show relatively large elongation of 1320% or more, but the maximum superplastic elongation was not obtained. The temperature was 825°C or higher, which is 25 to 50'C higher than that of the examples, and it was confirmed that the superplastic properties were clearly inferior to those of the examples. C7,cl
Although the temperature at which the maximum superplastic elongation was obtained for o was extremely low at 750'C, the superplastic elongation remained at 1300% and 780%, respectively, and the deformation stress was 2.85 kgr/*m', respectively.
2. The ivy has an extremely large value of 80 kgl'/g+v'. Also in C1, C2, C4, and C6,
The superplastic elongation was insufficient at around 1000%.
なお、C8は常温での伸びが6%と小さく実用に耐えな
いため、超塑性引張り試験を行ゎながった。Note that the elongation of C8 at room temperature was as small as 6%, making it unsuitable for practical use, so a superplastic tensile test was not conducted.
C1〜C14は製造条件及び0品粒径が本発明の範囲か
ら外れるものであり、C1〜C14は圧下比が本発明の
範囲から外れ、C14は最終熱間圧延加熱温度が本発明
の範囲から外れ、C15は再結晶熱処理温度が本発明の
範囲から外れるものであるため、微細粒等軸組織となら
ず、塑性伸びが550〜1380%と実施例の値よりも
劣っていることが確認された。なお、C12、C14及
びC15はα晶が等軸位にならずアスペクト比が3以上
の粗大な棒状晶となったため粒径を測定しなかった。For C1 to C14, the manufacturing conditions and zero particle size are outside the range of the present invention, for C1 to C14, the rolling reduction ratio is outside the range of the present invention, and for C14, the final hot rolling heating temperature is outside the range of the present invention. It was confirmed that C15 does not have a fine-grained equiaxed structure because the recrystallization heat treatment temperature is outside the range of the present invention, and the plastic elongation is 550 to 1380%, which is inferior to the values of the examples. Ta. The particle sizes of C12, C14, and C15 were not measured because the α-crystals were not equiaxed and became coarse rod-like crystals with an aspect ratio of 3 or more.
[発明の効果]
この発明によれば、優れた強度を維持しつつ、超塑性加
工温度が低く、超塑性加工時の変形抵抗が小さく、従来
のチタン合金よりも超塑性延びが大きいといった超塑性
加工性に優れたチタン合金及びその製造方法を提供する
ことができる。[Effects of the Invention] According to the present invention, superplastic properties such as low superplastic processing temperature, low deformation resistance during superplastic processing, and greater superplastic elongation than conventional titanium alloys are achieved while maintaining excellent strength. A titanium alloy with excellent workability and a method for manufacturing the same can be provided.
また、この発明に係るチタン合金は、これら優れた特性
を生かして、航空宇宙機器用材料を始めとして、超塑性
加工性に優れた高強度チタン合金として広く用いること
が可能である。Moreover, the titanium alloy according to the present invention can be widely used as a high-strength titanium alloy with excellent superplastic workability, including as a material for aerospace equipment, by taking advantage of these excellent properties.
更に、この発明に係るチタン合金は、変型抵抗が小さい
という特長から、超塑性を利用した加工法だけでム<、
恒温鍛造や通常の熱間鍛造、あるいは温間鍛造等の加工
法においても優れた加工性を有することは明らかであり
、極めて広範な適用が可能である。Furthermore, since the titanium alloy according to the present invention has a low deformation resistance, it can be processed using only a processing method that utilizes superplasticity.
It is clear that it has excellent workability in processing methods such as isothermal forging, normal hot forging, and warm forging, and can be applied to an extremely wide range of applications.
第1図は1.3x (Cr%)+(Mo%)の値と超塑
性伸びとの関係を示すグラフ、第2図はCrの含有量と
超塑性伸びとの関係を示すグラフ、第3図はMOの含有
量と超塑性伸びとの関係を示すグラフ、第4図はa晶粒
径と超塑性伸びとの関係を示すグラフである。Figure 1 is a graph showing the relationship between the value of 1.3x (Cr%) + (Mo%) and superplastic elongation, Figure 2 is a graph showing the relationship between Cr content and superplastic elongation, and Figure 3 is a graph showing the relationship between the Cr content and superplastic elongation. The figure is a graph showing the relationship between MO content and superplastic elongation, and FIG. 4 is a graph showing the relationship between a-crystal grain size and superplastic elongation.
Claims (3)
、α晶の平均粒径が6μm以下であることを特徴とする
超塑性加工性に優れたチタン合金。(1) In weight%, Al: 5.5 to 6.75% V: 3.5 to 4.5% O: 0.2% or less Cr: 0.85 to 3.15% Mo: 0.85 to 3.15% and satisfies the conditions of 3%≦{1.8×(Cr%)+(Mo%)}≦8%, the remainder consists of Ti and inevitable impurities, and the average of α crystals A titanium alloy with excellent superplastic workability characterized by a grain size of 6 μm or less.
チタン合金を、(β変態点−200℃)以上、β変態点
未満の温度で加熱し、引き続き、β変態点未満の温度で
圧下比を3以上とする圧下を施すことを特徴とする超塑
性加工性に優れたチタン合金の製造方法。(2) In weight%, Al: 5.5 to 6.75% V: 3.5 to 4.5% O: 0.2% or less Cr: 0.85 to 3.15% Mo: 0.85 to A titanium alloy containing 3.15% and satisfying the conditions of 3%≦{1.8×(Cr%)+(Mo%)}≦8%, with the balance consisting of Ti and unavoidable impurities ( Excellent superplastic workability, characterized by heating at a temperature of at least -200°C (beta transformation point) and less than the beta transformation point, followed by rolling at a rolling ratio of 3 or more at a temperature below the beta transformation point. Method of manufacturing titanium alloy.
チタン合金を、(β変態点−200℃)以上、β変態点
未満の温度で加熱し、引き続き、β変態点未満の温度で
圧下比を3以上とする圧下を施し、(β変態点−200
℃)以上、β変態点未満の温度で再結晶熱処理を施し、
超塑性加工を施すことを特徴とするチタン合金の超塑性
加工方法。(3) In weight%, Al: 5.5 to 6.75% V: 3.5 to 4.5% O: 0.2% or less Cr: 0.85 to 3.15% Mo: 0.85 to A titanium alloy containing 3.15% and satisfying the conditions of 3%≦{1.8×(Cr%)+(Mo%)}≦8%, with the balance consisting of Ti and unavoidable impurities ( Heating is carried out at a temperature not less than β-transformation point -200°C and less than β-transformation point, followed by rolling with a reduction ratio of 3 or more at a temperature below β-transformation point.
℃) or above and below the β transformation point,
A method for superplastic processing of titanium alloys, which is characterized by applying superplastic processing.
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP3742190A JPH0819503B2 (en) | 1990-02-20 | 1990-02-20 | Titanium alloy excellent in superplastic workability, method for producing the same, and superplastic workability method for titanium alloy |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP3742190A JPH0819503B2 (en) | 1990-02-20 | 1990-02-20 | Titanium alloy excellent in superplastic workability, method for producing the same, and superplastic workability method for titanium alloy |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| JPH03243740A true JPH03243740A (en) | 1991-10-30 |
| JPH0819503B2 JPH0819503B2 (en) | 1996-02-28 |
Family
ID=12497059
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP3742190A Expired - Fee Related JPH0819503B2 (en) | 1990-02-20 | 1990-02-20 | Titanium alloy excellent in superplastic workability, method for producing the same, and superplastic workability method for titanium alloy |
Country Status (1)
| Country | Link |
|---|---|
| JP (1) | JPH0819503B2 (en) |
Cited By (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| CN114346141A (en) * | 2022-01-17 | 2022-04-15 | 太原理工大学 | A multi-stage hot working method for preparing weak alpha textured titanium alloy forgings |
| EP4327964A1 (en) * | 2022-08-25 | 2024-02-28 | Rolls-Royce plc | Titanium alloy and methods of manufacture |
-
1990
- 1990-02-20 JP JP3742190A patent/JPH0819503B2/en not_active Expired - Fee Related
Cited By (3)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| CN114346141A (en) * | 2022-01-17 | 2022-04-15 | 太原理工大学 | A multi-stage hot working method for preparing weak alpha textured titanium alloy forgings |
| CN114346141B (en) * | 2022-01-17 | 2024-06-07 | 太原理工大学 | Multistage hot processing method for preparing weak alpha texture titanium alloy forging |
| EP4327964A1 (en) * | 2022-08-25 | 2024-02-28 | Rolls-Royce plc | Titanium alloy and methods of manufacture |
Also Published As
| Publication number | Publication date |
|---|---|
| JPH0819503B2 (en) | 1996-02-28 |
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