JPS59116356A - Molybdenum alloy - Google Patents
Molybdenum alloyInfo
- Publication number
- JPS59116356A JPS59116356A JP22401682A JP22401682A JPS59116356A JP S59116356 A JPS59116356 A JP S59116356A JP 22401682 A JP22401682 A JP 22401682A JP 22401682 A JP22401682 A JP 22401682A JP S59116356 A JPS59116356 A JP S59116356A
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- Prior art keywords
- alloy
- temperature
- temp
- small amount
- ingot
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Abstract
Description
【発明の詳細な説明】
〔発明の技術分野〕
本発明は高温強度が犬きく再結晶温度の高いモリブデン
合金に関する。DETAILED DESCRIPTION OF THE INVENTION [Technical Field of the Invention] The present invention relates to a molybdenum alloy that has excellent high-temperature strength and a high recrystallization temperature.
モリブデン合金は、真空、不活性及び還元性雰囲気中で
の高温安定性に優れているため、各種の血1熱材料とし
て使用され、最近では、核融合炉の炉壁iなど原子力分
野での用途が広がりつつある。Molybdenum alloys have excellent high-temperature stability in vacuum, inert, and reducing atmospheres, so they are used as a variety of heat-generating materials.Recently, molybdenum alloys are used for applications in the nuclear field, such as the reactor walls of fusion reactors. is expanding.
しかし、ながら、モリブデン合金は再結晶温度以」二に
加熱された後は、室温での延性が乏しくなり結晶粒界か
ら脆性破壊を生じ易すくなり、その強度が低下する。However, after a molybdenum alloy is heated above its recrystallization temperature, its ductility at room temperature becomes poor, and brittle fracture is more likely to occur at grain boundaries, resulting in a decrease in its strength.
このような問題を解決するものとしてモリブデンに少量
のバナジウムを含有させた合金が知られている。これは
、バナジウムをモリブデンに固溶させ合金の強度を高め
るとともに、結晶粒界に存在する粒界不純物(例えば酸
素)とバナジウムを反応させて結晶粒界を清浄化したも
のである。まだ、更に少量の炭素を添加して脱酸効果を
改善せしめた合金も知られている。As a solution to this problem, an alloy containing molybdenum and a small amount of vanadium is known. This improves the strength of the alloy by dissolving vanadium in molybdenum, and also cleans the grain boundaries by reacting vanadium with grain boundary impurities (such as oxygen) present in the grain boundaries. There are also alloys known in which the deoxidizing effect is improved by adding a small amount of carbon.
しかしながら、近時、モリブデン合金に要求される特性
が厳しくなる中で、−履古結晶温度が高く高温強度に優
れたモリブデン合金の開発が強く望まれている。However, in recent years, as the properties required of molybdenum alloys have become stricter, there has been a strong desire to develop molybdenum alloys that have a high aged crystallization temperature and excellent high-temperature strength.
本発明は再結晶温度が高く高温強度の大きい新規な組成
のモリブデン合金の提供を目的とする。The object of the present invention is to provide a molybdenum alloy with a novel composition that has a high recrystallization temperature and high high-temperature strength.
本発明のモリブデン合金は、ジルコニウム(Zr) 0
.02〜0.5重量%、ホウ素(B)5〜1001)p
m、残部がモリブデン(MO)であることを特徴とする
。The molybdenum alloy of the present invention contains zirconium (Zr) 0
.. 02-0.5% by weight, boron (B) 5-1001)p
m, the remainder being molybdenum (MO).
本発明のIIJI Q合金において、ZrはMOと固溶
し、又、ベースメタル中の酸素、炭素などと結合し、そ
れがベースメタル中に分散することによって、合金の機
械的強度、とりわけその高温強度を高めるとともに、再
結晶温度も高めかつ結晶粒の粗大化を抑制する成分であ
る。Zrの効果は0.02重−晒チからあられれるが、
その量が05重量%を超えると再結晶温度の上昇率は低
下するとともに得られた合金の加工性を悪くする。好ま
し1;tO,1〜02重@係である。In the IIJI Q alloy of the present invention, Zr forms a solid solution with MO, and also combines with oxygen, carbon, etc. in the base metal, and is dispersed in the base metal, thereby improving the mechanical strength of the alloy, especially its high temperature It is a component that not only increases strength but also increases recrystallization temperature and suppresses coarsening of crystal grains. The effect of Zr can be seen from 0.02 times bleaching, but
If the amount exceeds 0.5% by weight, the rate of increase in recrystallization temperature will decrease and the processability of the resulting alloy will deteriorate. Preferably 1; tO, 1 to 02 times.
Bは結晶粒界の清浄化に大きく寄与するとともに再結晶
後に結晶粒の粗大化を防止する成分である。このBの効
果は5ppm未満では粒界清浄化の効果が充分ではなく
、また1100ppを超えるとMo2Bが析出して粗大
化し合金を脆化せしめてし寸う。好寸しくは20〜s
o pprnである。B is a component that greatly contributes to cleaning grain boundaries and prevents coarsening of crystal grains after recrystallization. If the B content is less than 5 ppm, the grain boundary cleaning effect will not be sufficient, and if it exceeds 1100 ppm, Mo2B will precipitate and become coarse, leading to embrittlement of the alloy. Ideally 20~s
opprn.
本発明のMO合金は次のようにして製造することができ
る。すなわち、粒径3〜20μ7nのMo。The MO alloy of the present invention can be manufactured as follows. That is, Mo with a particle size of 3 to 20μ7n.
Zr I Bの粉末をそれぞれ所定量秤量し、これらを
例えば磁製ポットミルのような混合機中で充分に混合し
た後、得られた混合粉末をう・く−フ。After weighing a predetermined amount of Zr I B powder and thoroughly mixing them in a mixer such as a porcelain pot mill, the obtained mixed powder is made into a kufu.
レスなどで成形する。この成形体を常法に従って焼結し
た後、得られた焼結体を真空中でアーク溶解して合金化
する。Shape it with a cloth etc. After this compact is sintered according to a conventional method, the obtained sintered compact is arc melted in a vacuum to form an alloy.
なお、このとき、MOIZrlBの外に少量の、好まし
くは300ppm以下の炭素を添加すると、炭素による
脱酸効果とともにアーク溶解時にBの効果を一層助長す
ることがあって有用である。At this time, it is useful to add a small amount of carbon, preferably 300 ppm or less, in addition to MOIZrlB, since this can further promote the deoxidizing effect of carbon and the effect of B during arc melting.
しかし、残存炭素量が500ppm以上になると合金の
加工性が著しく悪くなるので注意すべきである。However, it should be noted that when the amount of residual carbon exceeds 500 ppm, the workability of the alloy deteriorates significantly.
かくして得られた合金のインゴットを熱間鍛造、熱間圧
延等所定の加工を施して各種の形状に加工し実用に供す
ることができる。The alloy ingot thus obtained can be subjected to predetermined processing such as hot forging and hot rolling to be processed into various shapes for practical use.
1)合金の製造
MO,Zr、BICの粉末(平均粒径6 μ+?z )
を所定の割合で配合し、これを磁製ポットローラーで混
合した後、3000kg/cnt2の圧でラノ(−プレ
スを用いて成形体とした。1) Alloy production MO, Zr, BIC powder (average particle size 6 μ+?z)
were blended in a predetermined ratio, mixed using a porcelain pot roller, and then formed into a molded product using a lano press at a pressure of 3000 kg/cnt2.
この成形体を1830Cの水素雰囲気中で7時間焼成し
、直径25mm長さ300 trvnの焼結体とし/こ
。こitを2本つなぎ合せ消耗電極真空アーク溶解法で
合金化し直径50 mrv、長さ200 mmのインゴ
ットとした。This molded body was fired in a hydrogen atmosphere at 1830C for 7 hours to form a sintered body with a diameter of 25 mm and a length of 300 trvn. Two pieces of this material were joined together and alloyed using a consumable electrode vacuum arc melting method to form an ingot with a diameter of 50 mrv and a length of 200 mm.
得られたMO合金の組成を表に示した。The composition of the obtained MO alloy is shown in the table.
表中、試料番号1〜6は本発明の合金、7は比較例であ
る。In the table, sample numbers 1 to 6 are alloys of the present invention, and sample number 7 is a comparative example.
上記したインゴットを常用の熱間鍛造、熱間圧延、冷間
圧延の処理を施こし、厚み1 mmの材料とした。The above-mentioned ingot was subjected to conventional hot forging, hot rolling, and cold rolling to obtain a material having a thickness of 1 mm.
2)特性の測定とその結果
各試料番号の板材を水素炉中で種々の温度で1時間焼鈍
し、その後、板利を室温にまで冷却し、これら板利のヴ
イツカース硬度(Hv)を測定した。その落果を第1図
に示した。2) Measurement of properties and results The plates of each sample number were annealed at various temperatures in a hydrogen furnace for 1 hour, then the plates were cooled to room temperature, and the Witzkers hardness (Hv) of these plates was measured. . Figure 1 shows the fallen fruit.
試料番号1〜5の板材につき、それぞiLのHVが加工
材と完全焼鈍材との中間の値を示すときの温度を第1図
から読み取り、その温度(半軟化温度)と板材のZr量
との関係をプロットし第2図を得た。For the plate materials of sample numbers 1 to 5, read the temperature at which the HV of iL shows an intermediate value between the processed material and the fully annealed material from Figure 1, and calculate that temperature (semi-softening temperature) and the Zr content of the plate material. Figure 2 was obtained by plotting the relationship between
つぎに、各板材を倍率200で顕微鏡観察し、単位面積
(0,0625+n+n2)の中に存在する再結晶粒の
数を計量し、その結果を焼鈍温度との関係として第3図
に示した。Next, each plate material was observed under a microscope at a magnification of 200, and the number of recrystallized grains present in a unit area (0,0625+n+n2) was measured, and the results are shown in FIG. 3 as a relationship with the annealing temperature.
試料番号1〜50板月につき、7.r量と再結晶粒径と
の関係を第3図から読みとり、第4図に示した。7. For each sample number 1 to 50 plates. The relationship between the amount of r and the recrystallized grain size was read from FIG. 3 and is shown in FIG. 4.
ついで、試料番号2,4及び7の板材につき、1400
t:で1時間焼鈍したのち、これらの各温度におけろ
引張り強度(MPa、)を測定し、その結果を第5図に
示した。Then, for the plate materials of sample numbers 2, 4 and 7, 1400
After annealing at t: for 1 hour, the tensile strength (MPa) was measured at each of these temperatures, and the results are shown in FIG.
第1図から明らかなように、本発明のMo合金は硬度が
高く、すなわち再結晶温度の高いことがわかる。壕だ、
第2図及び第3図からZr量が増すと半軟化温度が上昇
、すなわち、再結晶温度が高くなりかつ再結晶粒が小さ
くなることがわかる。As is clear from FIG. 1, the Mo alloy of the present invention has high hardness, that is, a high recrystallization temperature. It's a trench.
It can be seen from FIGS. 2 and 3 that as the amount of Zr increases, the semi-softening temperature increases, that is, the recrystallization temperature increases and the recrystallized grains become smaller.
しかも、第5図から明らかなように、本発明の合金は純
Moに比べてその高71情強度に浸れていることがわか
る。Moreover, as is clear from FIG. 5, the alloy of the present invention has a higher 71 strength than pure Mo.
本発明のMO合金は、その再結晶温度が高く、高温強度
も大きいので高温剛熱利料としての有用性に富むもので
ある。The MO alloy of the present invention has a high recrystallization temperature and high high-temperature strength, so it is highly useful as a high-temperature heating material.
第1図は実施例で用いた板拐の焼鈍温度とヴイツカース
硬度との関係を表わす図、第2図は半軟化温度とZr量
との関係を表わす図、第3図は焼鈍温度と再結晶粒径と
の関係図、第4図は7.r量と再結晶粒径との関係図、
第5図は各温度における引張り強度を表わす図である。
弔41〜R
t
Zr量(束髪%)−
第5図
八・状壕支(’C)−
手続補正書
口召和58年1月24日
特許庁長官 若 杉 和 夫 殿
1、事件の表示
昭和57年 特詐 願第 224016 号2、発明
の名称
モリブデン合金
3、補正をする者
事件との関係 特詐出願人
名 称 (307)東京芝浦電気株式会社(氏 名)
4、代 理 人Figure 1 is a diagram showing the relationship between the annealing temperature and Witzkars hardness of the board used in the examples, Figure 2 is a diagram showing the relationship between semi-softening temperature and Zr content, and Figure 3 is the relationship between annealing temperature and recrystallization. The relationship diagram with particle size, Figure 4 is 7. Relationship diagram between r amount and recrystallized grain size,
FIG. 5 is a diagram showing the tensile strength at each temperature. Funeral 41 ~ R t Zr amount (% of hair) - Figure 5 8. Shape ('C) - Procedural amendment document January 24, 1958 Kazuo Wakasugi, Commissioner of the Patent Office 1, Indication of the incident 1981 Special Fraud Application No. 224016 2 Name of the invention Molybdenum Alloy 3 Relationship with the person making the amendment Name of the special fraud applicant (307) Tokyo Shibaura Electric Co., Ltd. (Name) 4 Agent
Claims (1)
〜1100pp 、残部がモリブデンであることを特徴
とするモリブデン合金。Zirconium 002-05 heavy i' [L% + boron 5
A molybdenum alloy characterized in that 1100pp and the remainder are molybdenum.
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP22401682A JPS59116356A (en) | 1982-12-22 | 1982-12-22 | Molybdenum alloy |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP22401682A JPS59116356A (en) | 1982-12-22 | 1982-12-22 | Molybdenum alloy |
Publications (2)
Publication Number | Publication Date |
---|---|
JPS59116356A true JPS59116356A (en) | 1984-07-05 |
JPS6221066B2 JPS6221066B2 (en) | 1987-05-11 |
Family
ID=16807260
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
JP22401682A Granted JPS59116356A (en) | 1982-12-22 | 1982-12-22 | Molybdenum alloy |
Country Status (1)
Country | Link |
---|---|
JP (1) | JPS59116356A (en) |
Cited By (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
CN102085538A (en) * | 2010-12-24 | 2011-06-08 | 金堆城钼业股份有限公司 | Preparation method of silicon, aluminum, potassium and molybdenum alloy wire |
CN113975470A (en) * | 2021-11-22 | 2022-01-28 | 山东瑞安泰医疗技术有限公司 | Preparation method of degradable metal molybdenum-based alloy intravascular stent |
Families Citing this family (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
AT15903U1 (en) * | 2017-09-29 | 2018-08-15 | Plansee Se | Molybdenum sintered part |
-
1982
- 1982-12-22 JP JP22401682A patent/JPS59116356A/en active Granted
Cited By (3)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
CN102085538A (en) * | 2010-12-24 | 2011-06-08 | 金堆城钼业股份有限公司 | Preparation method of silicon, aluminum, potassium and molybdenum alloy wire |
CN113975470A (en) * | 2021-11-22 | 2022-01-28 | 山东瑞安泰医疗技术有限公司 | Preparation method of degradable metal molybdenum-based alloy intravascular stent |
CN113975470B (en) * | 2021-11-22 | 2023-09-22 | 山东瑞安泰医疗技术有限公司 | Preparation method of degradable metal molybdenum-base alloy intravascular stent |
Also Published As
Publication number | Publication date |
---|---|
JPS6221066B2 (en) | 1987-05-11 |
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