JPH03197632A - Intermetallic compound tial-fe base alloy - Google Patents
Intermetallic compound tial-fe base alloyInfo
- Publication number
- JPH03197632A JPH03197632A JP33579589A JP33579589A JPH03197632A JP H03197632 A JPH03197632 A JP H03197632A JP 33579589 A JP33579589 A JP 33579589A JP 33579589 A JP33579589 A JP 33579589A JP H03197632 A JPH03197632 A JP H03197632A
- Authority
- JP
- Japan
- Prior art keywords
- intermetallic compound
- titanium
- atoms
- iron
- compressive
- 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
- 229910045601 alloy Inorganic materials 0.000 title claims abstract description 13
- 239000000956 alloy Substances 0.000 title claims abstract description 13
- 229910000765 intermetallic Inorganic materials 0.000 title claims abstract description 9
- 229910052719 titanium Inorganic materials 0.000 claims abstract description 16
- 229910052742 iron Inorganic materials 0.000 claims abstract description 13
- 229910052782 aluminium Inorganic materials 0.000 claims abstract description 5
- XEEYBQQBJWHFJM-UHFFFAOYSA-N iron Substances [Fe] XEEYBQQBJWHFJM-UHFFFAOYSA-N 0.000 claims description 31
- 239000010936 titanium Substances 0.000 claims description 20
- RTAQQCXQSZGOHL-UHFFFAOYSA-N Titanium Chemical compound [Ti] RTAQQCXQSZGOHL-UHFFFAOYSA-N 0.000 claims description 15
- XAGFODPZIPBFFR-UHFFFAOYSA-N aluminium Chemical compound [Al] XAGFODPZIPBFFR-UHFFFAOYSA-N 0.000 claims description 4
- 238000000034 method Methods 0.000 abstract description 13
- 238000005096 rolling process Methods 0.000 abstract description 6
- 238000005242 forging Methods 0.000 abstract description 5
- 238000005728 strengthening Methods 0.000 abstract description 2
- 239000007787 solid Substances 0.000 abstract 1
- 239000000203 mixture Substances 0.000 description 11
- 238000002844 melting Methods 0.000 description 8
- 230000008018 melting Effects 0.000 description 8
- 238000012360 testing method Methods 0.000 description 8
- 230000000052 comparative effect Effects 0.000 description 7
- 230000006835 compression Effects 0.000 description 6
- 238000007906 compression Methods 0.000 description 6
- 238000012669 compression test Methods 0.000 description 5
- 238000012545 processing Methods 0.000 description 5
- 239000006104 solid solution Substances 0.000 description 5
- XKRFYHLGVUSROY-UHFFFAOYSA-N Argon Chemical compound [Ar] XKRFYHLGVUSROY-UHFFFAOYSA-N 0.000 description 4
- AZDRQVAHHNSJOQ-UHFFFAOYSA-N alumane Chemical group [AlH3] AZDRQVAHHNSJOQ-UHFFFAOYSA-N 0.000 description 4
- 230000000694 effects Effects 0.000 description 4
- 238000003754 machining Methods 0.000 description 4
- 239000000126 substance Substances 0.000 description 4
- 239000000654 additive Substances 0.000 description 3
- 230000000996 additive effect Effects 0.000 description 3
- 229910002056 binary alloy Inorganic materials 0.000 description 3
- 239000013078 crystal Substances 0.000 description 3
- 238000005516 engineering process Methods 0.000 description 3
- 238000000465 moulding Methods 0.000 description 3
- IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 description 2
- 229910010038 TiAl Inorganic materials 0.000 description 2
- 229910052786 argon Inorganic materials 0.000 description 2
- QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical compound [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 description 2
- 238000011109 contamination Methods 0.000 description 2
- RKTYLMNFRDHKIL-UHFFFAOYSA-N copper;5,10,15,20-tetraphenylporphyrin-22,24-diide Chemical compound [Cu+2].C1=CC(C(=C2C=CC([N-]2)=C(C=2C=CC=CC=2)C=2C=CC(N=2)=C(C=2C=CC=CC=2)C2=CC=C3[N-]2)C=2C=CC=CC=2)=NC1=C3C1=CC=CC=C1 RKTYLMNFRDHKIL-UHFFFAOYSA-N 0.000 description 2
- 238000013461 design Methods 0.000 description 2
- 238000010586 diagram Methods 0.000 description 2
- 238000010438 heat treatment Methods 0.000 description 2
- 238000000265 homogenisation Methods 0.000 description 2
- 239000012535 impurity Substances 0.000 description 2
- 229910052738 indium Inorganic materials 0.000 description 2
- 239000001301 oxygen Substances 0.000 description 2
- 229910052760 oxygen Inorganic materials 0.000 description 2
- 238000003672 processing method Methods 0.000 description 2
- 239000002994 raw material Substances 0.000 description 2
- 238000005204 segregation Methods 0.000 description 2
- 235000004348 Perilla frutescens Nutrition 0.000 description 1
- 244000124853 Perilla frutescens Species 0.000 description 1
- 238000004458 analytical method Methods 0.000 description 1
- 238000013459 approach Methods 0.000 description 1
- 238000005520 cutting process Methods 0.000 description 1
- 230000007423 decrease Effects 0.000 description 1
- 239000003779 heat-resistant material Substances 0.000 description 1
- 229910052751 metal Inorganic materials 0.000 description 1
- 239000002184 metal Substances 0.000 description 1
- 239000007769 metal material Substances 0.000 description 1
- 150000002739 metals Chemical class 0.000 description 1
- 229910052757 nitrogen Inorganic materials 0.000 description 1
- 230000003647 oxidation Effects 0.000 description 1
- 238000007254 oxidation reaction Methods 0.000 description 1
- 238000005498 polishing Methods 0.000 description 1
- 239000000843 powder Substances 0.000 description 1
- 238000011160 research Methods 0.000 description 1
- 238000007493 shaping process Methods 0.000 description 1
- 229910000601 superalloy Inorganic materials 0.000 description 1
Landscapes
- Forging (AREA)
- Powder Metallurgy (AREA)
Abstract
Description
【発明の詳細な説明】
〔産業上の利用分野〕
本発明は、軽量かつ高温強度に優れたTiAji系金属
間化合物に関し、特に該金属間化合物の変形特性を向上
させるために成分制御を施した合金系に関する。[Detailed Description of the Invention] [Field of Industrial Application] The present invention relates to a TiAji-based intermetallic compound that is lightweight and has excellent high-temperature strength, and in particular to a TiAji-based intermetallic compound that has been subjected to component control in order to improve the deformation characteristics of the intermetallic compound. Regarding alloy systems.
耐熱材料として実用化の期待されている金属間化合物T
iAj!は、展延性に乏しいために加工が難しい。Ti
Aj!の実用化のための最大の障害であるこの低加工性
改善のための手法は、大別して加工プロセスの応用と合
金設計が挙げられる。低加工性とは主として室温におけ
る延性の欠如を指し、Tilは圧延、鍛造といった従来
行なわれている加工法を直接室温で適用することはでき
ない。Intermetallic compound T expected to be put into practical use as a heat-resistant material
iAj! is difficult to process due to its poor malleability. Ti
Aj! Methods for improving this low formability, which is the biggest obstacle to practical application, can be broadly divided into machining process application and alloy design. Low workability mainly refers to lack of ductility at room temperature, and conventional processing methods such as rolling and forging cannot be directly applied to Til at room temperature.
加工プロセス適用の場合、粉末加工法に代表されるニア
−・ネット・シェイプ化から従来の圧延、鍛造といった
加工法も含む。これまでにCo基超超合金S−816)
を用いての高温シース圧延(x00℃、圧延速度: 1
.5 m/m1n)による成型(特開昭61−2133
61号公報)や、800℃以上、歪速度10−” 5e
c−’以下における恒温鍛造(特開昭63−17186
2号公報)等による加工形状付与化が報告されている。When applied to machining processes, it includes near-net shaping typified by powder machining, as well as conventional machining methods such as rolling and forging. Until now, Co-based superalloy S-816)
High temperature sheath rolling using (x00℃, rolling speed: 1
.. 5 m/m1n) (Japanese Patent Application Laid-Open No. 61-2133
61 Publication), 800°C or higher, strain rate 10-” 5e
Constant temperature forging below c-' (JP-A-63-17186
It has been reported that processing shapes can be imparted by methods such as Publication No. 2).
こうした加工法の特徴は、TiA[の800℃以上に詔
ける延性能の発現を利用したものであり、Tilの機械
的性質に及ぼす歪速度依存性と併用することにより、成
型加工を可能にしている。但し充分な成型加工を行なう
ための加工条件が、1000℃以上の高温であること、
更に歪速度をできるだけ低減化させなくてはならないこ
とから、大型設備の適用が必ずしも容易では無いという
欠点を有する。The feature of this processing method is that it takes advantage of the ductility of TiA that can reach temperatures above 800°C, and when used in conjunction with the strain rate dependence of TiA's mechanical properties, it enables molding. There is. However, the processing conditions for sufficient molding processing must be a high temperature of 1000°C or higher.
Furthermore, since the strain rate must be reduced as much as possible, it has the disadvantage that it is not necessarily easy to apply large-scale equipment.
一方、Ti と、lの混合、圧粉成型後、高温高圧処理
による成型化が報告されている(特開昭63−1400
49号公報)。この法は上δ己加エプロセスとは異なり
、成型化と同時に様々な形への形状加工化が可能である
ことを長所とする反面、問題点としてT1やAlといっ
た活性金属を用いることによる不純物混入が不可避であ
るという点が指摘される。On the other hand, it has been reported that Ti and L are mixed, compacted, and then formed by high-temperature and high-pressure treatment (Japanese Patent Application Laid-Open No. 63-1400
Publication No. 49). This method is different from the upper δ self-adding process, and has the advantage of being able to be shaped into various shapes at the same time as molding. However, the problem is that the use of active metals such as T1 and Al causes impurities. It is pointed out that contamination is inevitable.
これに対して添加元素による室温延性改善の報告は、U
nited Technology Carp、 に
よるV添加(特開昭56−41344号公報)、金属材
料技術研究所によるMn添加(特開昭61−41740
号公報)、Ag添加(特開昭58−123847号公報
)、そしてGeneral巳1ectric Corp
、によるS1添加(米国特許第4836983号公報)
、Ta添加(米国特許第4842817号公報)、C
r添加(米国特許第4f142819号公報)、B添加
(米国特許第4842820号公報)が挙げられる。ま
た、高温延性改善のために、0.005〜0.2重1%
B添加(特開昭63−x4930号公報)、あるいは0
.02〜0.3重量%Bと0.2〜5.0重量%Siを
複合添加(特開昭63−125634号公報)した報告
がある。これらの添加元素の効果は、低性能改善に加え
、耐酸化性の改善や耐クリープ特性の改善も含めて、幅
広い合金成分調整が行なわれている。On the other hand, there have been reports of improvement in room temperature ductility due to additive elements.
V addition (Japanese Unexamined Patent Publication No. 56-41344) by nited Technology Carp, Mn addition (Japanese Unexamined Patent Publication No. 61-41740) by Metal Materials Technology Research Institute.
No. 1), Ag addition (Japanese Patent Application Laid-open No. 123847/1983), and General Electric Corp.
, S1 addition (US Pat. No. 4,836,983)
, Ta addition (US Pat. No. 4,842,817), C
Examples include r addition (US Pat. No. 4F142819) and B addition (US Pat. No. 4,842,820). In addition, to improve high-temperature ductility, 0.005 to 0.2 weight 1%
B addition (Japanese Unexamined Patent Publication No. 63-x4930) or 0
.. There is a report on the combined addition of 02 to 0.3% by weight B and 0.2 to 5.0% by weight Si (Japanese Patent Application Laid-open No. 125634/1983). The effects of these additive elements include not only improvements in low performance but also improvements in oxidation resistance and creep resistance, resulting in a wide range of alloy component adjustments.
延性能の目安は室温引張伸び値が3.0%といわれてい
るが、どの添加元素の選択による成分設計法によっても
未だ達成されておらず、加工プロセスとの併用による微
細化等の組織制御を通した対応が不可欠と考えられる。The standard for ductility performance is said to be a room temperature tensile elongation value of 3.0%, but this has not yet been achieved by any compositional design method based on the selection of additive elements, and microstructural control such as refinement by combining with processing processes is required. It is considered essential to respond through these measures.
本発明の目的は、金属間化合物TiA1’基合金の成分
設計を行なうことにより、圧縮変形特性に優れ、同時に
組織制御の可能な実用性の高い合金を提供することにあ
る。An object of the present invention is to provide a highly practical alloy that has excellent compressive deformation properties and is also capable of microstructural control by designing the composition of an intermetallic compound TiA1'-based alloy.
上記の目的を達成させるTiAA’基合金は、基本組成
としてチタン、アルミニウム、及び鉄とし、原子分率成
分を用いると次式によって表示される。A TiAA'-based alloy that achieves the above object has titanium, aluminum, and iron as its basic composition, and is expressed by the following formula using atomic fraction components.
ここでX・yはチタンと鉄の原子分率を指す。Here, X.y refers to the atomic fraction of titanium and iron.
Ti、A RI−M−’yFey 但し 0.50≦
x≦0.520.005≦y≦0.04
0.505≦x+y≦0.55
以下本発明につき詳細に説明する。Ti, ARI-M-'yFey However, 0.50≦
x≦0.520.005≦y≦0.04 0.505≦x+y≦0.55 The present invention will be described in detail below.
溶解原料としては、高純度チタンと高純度アルミニウム
及び高純度鉄を用い、酸素、窒素等の気体不純物の混入
を回避す6ために、好ましくはチタンゲッター同時溶解
による高真空雰囲気制御可能な多極式アルゴンアーク溶
解法により、TiAA−Fe基合金を溶製する。成分元
素の偏析による不均質性を防止するためには、多数回溶
解を行なった方が良く、更に1050℃で48時間程度
の均質化熱処理を、I Xl0−’Torr以上の高真
空下で行なう。High-purity titanium, high-purity aluminum, and high-purity iron are used as melting raw materials, and in order to avoid contamination with gaseous impurities such as oxygen and nitrogen, it is preferable to use a multi-electrode that can control a high vacuum atmosphere by simultaneously melting a titanium getter. A TiAA-Fe-based alloy is melted using the argon arc melting method. In order to prevent heterogeneity due to segregation of component elements, it is better to perform melting multiple times, and further perform homogenization heat treatment at 1050°C for about 48 hours under high vacuum of IXl0-'Torr or higher. .
本発明のTil基合金の成分が上記のように限定される
理由は以下の通りである。The reason why the components of the Til-based alloy of the present invention are limited as described above is as follows.
チタン:50〜52原子%
TiAl1の単相領域は、チタンが室温において45.
0〜51.0原子%の範囲内であり、それよりチタン過
剰側ではTi、A flが、アルミニウム過剰側ではT
iAl2が晶出する。Ti −に元系における室温圧縮
試験によれば、化学量論組成よりもわずかにチタン過剰
側で圧縮特性が優れている。これらのことから、圧縮特
性に優れた組成はTi、Al2の体積分率が10%以下
の上記組成とし、さらに高圧縮特性を安定して得るため
には、チタンは50〜51原子%が好ましい。Titanium: 50 to 52 atomic% In the single phase region of TiAl1, titanium is 45% at room temperature.
Within the range of 0 to 51.0 at%, Ti and A fl are on the titanium-excess side, and T is on the aluminum-excess side.
iAl2 crystallizes out. According to a room temperature compression test in a Ti - based system, the compression properties are superior when the titanium content is slightly more than the stoichiometric composition. For these reasons, the composition with excellent compression properties is the above composition in which the volume fraction of Ti and Al2 is 10% or less, and in order to stably obtain high compression properties, titanium is preferably 50 to 51 atomic %. .
鉄:0.5〜4原子% 鉄添加は組織の微細化を施す以外に、TiAlのLl。Iron: 0.5-4 atomic% In addition to making the structure finer, the addition of iron also improves the Ll of TiAl.
型構造(正方晶)に起因するc / aを、鉄添加によ
り1に近づけることから、正方晶格子から面心立方晶格
子に近づき、TiAji!のもつ結晶異方性を低下させ
る効果がある。その固溶量は3原子%以下と少ないが、
4原子%までは上言己効果を有し、それを越えると第二
相の体積分率が著しく増加すると同時に、微細化の効果
も低減する。Since c/a caused by the type structure (tetragonal) is brought closer to 1 by adding iron, the tetragonal lattice approaches a face-centered cubic lattice, and TiAji! It has the effect of reducing the crystal anisotropy of The amount of solid solution is small at less than 3 at%, but
Up to 4 atomic %, there is a self-effect, and beyond that, the volume fraction of the second phase increases significantly, and at the same time, the refinement effect decreases.
本発明における成分制御のもう一つの特徴は、鉄原子を
TiA[のアルミニウム原子と置換させて固溶させてい
る点にあり、チタンと鉄の原子分率をそれぞれx、yと
すると、次式によって表示される。Another feature of component control in the present invention is that iron atoms are substituted with aluminum atoms in TiA to form a solid solution.If the atomic fractions of titanium and iron are x and y, respectively, the following equation displayed by.
Ti、Ax−x−yFey 但し 0.50≦x≦0
.520.005 ≦y≦0.04
0.505 ≦x+y≦0.55
本発明の要点は、鉄原子は結晶格子上でアルミニウム原
子と相互置換をするように配合している場合にのみ、圧
縮特性が改善されることを見出したことに基づくもので
ある。即ち、本発明の合金系の化学式は下式の様に表記
される(これを【タイプl]とする)。言い替えれば、
鉄原子をチタン原子と置換させているような場合(化学
式を【タイプ2]とする)や、チタンとアルミニウム原
子両方と置換するような場合(化学式を【タイプ3]と
する)とは異なる固溶形態を示している。Ti, Ax-x-yFey However, 0.50≦x≦0
.. 520.005 ≦y≦0.04 0.505 ≦x+y≦0.55 The key point of the present invention is that the compressive properties are improved only when iron atoms are mixed so as to mutually substitute with aluminum atoms on the crystal lattice. This is based on the discovery that the That is, the chemical formula of the alloy system of the present invention is expressed as the following formula (this is referred to as [Type I]). In other words,
This is different from cases where an iron atom is replaced with a titanium atom (the chemical formula is [Type 2]) or when both titanium and aluminum atoms are substituted (the chemical formula is [Type 3]). Shows the dissolved form.
【タイプx Ti(AA 、 Fe)【タイプ2]
(Ti 、、Fe)Ai【タイプ3]
(Ti 、Fe)(Aj! 、Fe)TiAl系金
属間化合物の組成範囲を本発明の範囲に特定することに
よりタイプ1となって、組織は粒径が微細化し等軸晶が
発達しやすくなる。また圧縮変形に対する降伏応力及び
破壊応力が向上し、圧縮率も向上して変形しやすくなる
。タイプ2及びタイプ3では本発明のような圧縮特性の
向上は認められない。[Type x Ti (AA, Fe) [Type 2]
(Ti,,Fe)Ai [Type 3]
(Ti, Fe) (Aj!, Fe) By specifying the composition range of the TiAl intermetallic compound within the range of the present invention, it becomes Type 1, and the grain size of the structure becomes fine and equiaxed crystals tend to develop. . Furthermore, the yield stress and fracture stress against compressive deformation are improved, the compressibility is also improved, and deformation becomes easier. In Type 2 and Type 3, no improvement in compression properties as in the present invention is observed.
純度99.9%の高純度チタン(酸素量400ppm以
下)50〜51原子%、純度99.99%のアルミニウ
ム46〜49原子%、及び純度99.99%の高純度鉄
1〜3原子%からなる溶解原料を、高真空雰囲気制御可
能な多極式アルゴンアーク溶解法により溶製した。From high-purity titanium with a purity of 99.9% (oxygen content 400 ppm or less) 50 to 51 at%, aluminum with a purity of 99.99% from 46 to 49 at%, and high-purity iron with a purity of 99.99% from 1 to 3 at% The melted raw material was melted using a multipolar argon arc melting method that can control a high vacuum atmosphere.
溶解に際しては成分元素のマクロ偏析を回避するために
3回溶解を行ない、1050℃で48時間の均質化熱処
理をI X 1O−5Torr以上の高真空下で行った
。During melting, melting was performed three times to avoid macro segregation of component elements, and homogenization heat treatment was performed at 1050° C. for 48 hours under high vacuum of I x 10-5 Torr or more.
溶製インゴットから断面が3mmφで高さ4.5 mm
の圧縮試験片をワイヤーカット装置で採取し、圧縮面を
精密平行研磨した後に、インストロン型試験機を用いて
室温圧縮試験を行なった。圧縮試験の信頼度を向上させ
るために試験は5回行なったものの平均値をとり、各機
械的特性値のバラツキ精度は最大、最小値が平均値から
15%以内とした。The cross section from the melted ingot is 3 mmφ and the height is 4.5 mm.
A compression test piece was taken using a wire cutting device, and after precision parallel polishing of the compression surface, a room temperature compression test was conducted using an Instron type testing machine. In order to improve the reliability of the compression test, the test was conducted five times and the average value was taken, and the maximum and minimum variation accuracy of each mechanical property value was within 15% from the average value.
なおここでいう圧縮率は((試験片の初期高さ)−(応
力・歪線図で試験片が破断する直前の試験片の高さ))
/(試験片の初期高さ) X100とする。また圧縮破
断強度は応力・歪線図上で試験片が破断する直前の荷重
を初期断面積で除した値とする。The compression ratio here is ((initial height of the test piece) - (height of the test piece just before it breaks in the stress/strain diagram))
/(Initial height of test piece) shall be X100. The compressive breaking strength is the value obtained by dividing the load immediately before the specimen breaks by the initial cross-sectional area on the stress-strain diagram.
本発明の上記実施例を第1表及び第2表に表示した。第
1表はその試験試料組成の化学分析値を示し、第2表は
圧縮試験結果を示す。また、下記に示す比較例(1)〜
(3)も同時、に、上記各表に表示した。各比較例での
試験試料の溶製方法及び試験方法は上記実施例と同様に
した。The above examples of the present invention are shown in Tables 1 and 2. Table 1 shows the chemical analysis values of the test sample composition, and Table 2 shows the compression test results. In addition, the following comparative examples (1) to
(3) is also shown in each table above at the same time. The melting method and testing method for test samples in each comparative example were the same as in the above examples.
すなわち比較例(1)はTiAβ二元系の試料であり、
比較例(2)はTiA!二元系において鉄原子がチタン
原子と置換するよう、上記タイプ2の固溶形態をとるよ
うに添加したもので、これらの組成は原子分率表記によ
る下記式の組成範囲に相当する。That is, Comparative Example (1) is a TiAβ binary system sample,
Comparative example (2) is TiA! They are added so that iron atoms replace titanium atoms in the binary system, forming a solid solution form of the type 2 described above, and these compositions correspond to the composition range of the following formula expressed as atomic fractions.
TI>IA j! I−X−yFe、 但し 0.4
5≦x≦0.4950.005 ≦y≦0.04
0.49≦x+y≦0.51
また、比較例(3)はTiAj!二元系において鉄原子
がチタン原子とアルミニウム原子双方と置換するよう、
上記タイプ3の固溶形態をとるように添加した。これら
の組成は原子分率表記による下記式の組成範囲に相当す
る。TI>IA j! I-X-yFe, however, 0.4
5≦x≦0.4950.005 ≦y≦0.04 0.49≦x+y≦0.51 Comparative example (3) is TiAj! In the binary system, iron atoms replace both titanium atoms and aluminum atoms,
It was added so as to take the solid solution form of Type 3 above. These compositions correspond to the composition range of the following formula expressed in atomic fraction.
TixA l 1−x−yFey 但し 0.46≦
x≦0.500.01≦y≦0.05
0.51<x+y≦0.55
以上の本発明の実施例と各比較例とを比較すると、各比
較例はいずれも本発明の実施例の破断応力及び圧縮特性
より劣っていることが判明した。TixA l 1-x-yFey However, 0.46≦
x≦0.500.01≦y≦0.05 0.51<x+y≦0.55 Comparing the above examples of the present invention and each comparative example, each comparative example is different from the example of the present invention. It was found that the breaking stress and compressive properties were inferior.
第
1
表
く原子%)
第
表
〔発明の効果〕
本発明は、圧縮変形特性を向上させると同時に、鉄元素
添加による固溶体強化も可能なことから、機械的性質を
総じて向上させることができ、圧縮応力が支配的な圧延
、鍛造といった加工プロセスへの適用に有利になった。Table 1 (Atomic %) Table [Effects of the Invention] The present invention improves the compressive deformation characteristics and at the same time enables solid solution strengthening by adding iron elements, so it is possible to improve the mechanical properties as a whole. It has become advantageous for application to processing processes such as rolling and forging where compressive stress is dominant.
更に添加元素量は微量であることから、TiAf!のも
つ従来の軽量性を損なっていないことから、航空機部材
への適用も可能になると考えられる。Furthermore, since the amount of added elements is very small, TiAf! It is thought that it will also be possible to apply it to aircraft parts because it does not impair the conventional lightweight properties.
Claims (1)
下記式によって原子分率成分表示されることを特徴とす
る圧縮変形特性に優れた金属間化合物TiAl−Fe基
合金。 Ti_xAl_1_−_x_−_yFe_y但し0.5
0≦x≦0.520.005≦y≦0.04 0.505≦x+y≦0.55[Scope of Claims] An intermetallic compound TiAl-Fe-based alloy having excellent compressive deformation characteristics, comprising titanium, aluminum, and iron, and characterized in that the above elements are expressed as atomic fraction components according to the following formula. Ti_xAl_1_-_x_-_yFe_yHowever, 0.5
0≦x≦0.520.005≦y≦0.04 0.505≦x+y≦0.55
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP33579589A JP2735331B2 (en) | 1989-12-25 | 1989-12-25 | Intermetallic compound TiA ▲ -Fe-based alloy |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP33579589A JP2735331B2 (en) | 1989-12-25 | 1989-12-25 | Intermetallic compound TiA ▲ -Fe-based alloy |
Publications (2)
Publication Number | Publication Date |
---|---|
JPH03197632A true JPH03197632A (en) | 1991-08-29 |
JP2735331B2 JP2735331B2 (en) | 1998-04-02 |
Family
ID=18292517
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
JP33579589A Expired - Lifetime JP2735331B2 (en) | 1989-12-25 | 1989-12-25 | Intermetallic compound TiA ▲ -Fe-based alloy |
Country Status (1)
Country | Link |
---|---|
JP (1) | JP2735331B2 (en) |
Cited By (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
CN102634790A (en) * | 2012-05-03 | 2012-08-15 | 华北电力大学 | Fe-Ti and Fe-Al complex-phase intermetallic compound anti-corrosion layer and preparation method thereof |
-
1989
- 1989-12-25 JP JP33579589A patent/JP2735331B2/en not_active Expired - Lifetime
Cited By (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
CN102634790A (en) * | 2012-05-03 | 2012-08-15 | 华北电力大学 | Fe-Ti and Fe-Al complex-phase intermetallic compound anti-corrosion layer and preparation method thereof |
Also Published As
Publication number | Publication date |
---|---|
JP2735331B2 (en) | 1998-04-02 |
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