JPS6221066B2 - - Google Patents
Info
- Publication number
- JPS6221066B2 JPS6221066B2 JP22401682A JP22401682A JPS6221066B2 JP S6221066 B2 JPS6221066 B2 JP S6221066B2 JP 22401682 A JP22401682 A JP 22401682A JP 22401682 A JP22401682 A JP 22401682A JP S6221066 B2 JPS6221066 B2 JP S6221066B2
- Authority
- JP
- Japan
- Prior art keywords
- alloy
- temperature
- molybdenum
- strength
- recrystallization
- 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.)
- Expired
Links
- 229910001182 Mo alloy Inorganic materials 0.000 claims description 12
- 238000001953 recrystallisation Methods 0.000 claims description 9
- 229910052750 molybdenum Inorganic materials 0.000 claims description 6
- 229910052796 boron Inorganic materials 0.000 claims description 5
- ZOKXTWBITQBERF-UHFFFAOYSA-N Molybdenum Chemical compound [Mo] ZOKXTWBITQBERF-UHFFFAOYSA-N 0.000 claims description 4
- 239000011733 molybdenum Substances 0.000 claims description 4
- 229910052726 zirconium Inorganic materials 0.000 claims description 4
- ZOXJGFHDIHLPTG-UHFFFAOYSA-N Boron Chemical compound [B] ZOXJGFHDIHLPTG-UHFFFAOYSA-N 0.000 claims description 2
- QCWXUUIWCKQGHC-UHFFFAOYSA-N Zirconium Chemical compound [Zr] QCWXUUIWCKQGHC-UHFFFAOYSA-N 0.000 claims 1
- 229910045601 alloy Inorganic materials 0.000 description 10
- 239000000956 alloy Substances 0.000 description 10
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 description 5
- 229910052799 carbon Inorganic materials 0.000 description 5
- 238000010586 diagram Methods 0.000 description 5
- 229910052720 vanadium Inorganic materials 0.000 description 3
- LEONUFNNVUYDNQ-UHFFFAOYSA-N vanadium atom Chemical compound [V] LEONUFNNVUYDNQ-UHFFFAOYSA-N 0.000 description 3
- 238000000137 annealing Methods 0.000 description 2
- QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical compound [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 description 2
- 239000010953 base metal Substances 0.000 description 2
- 238000004140 cleaning Methods 0.000 description 2
- 239000013078 crystal Substances 0.000 description 2
- 239000003779 heat-resistant material Substances 0.000 description 2
- 239000000463 material Substances 0.000 description 2
- 238000002844 melting Methods 0.000 description 2
- 230000008018 melting Effects 0.000 description 2
- 239000000203 mixture Substances 0.000 description 2
- 229910052760 oxygen Inorganic materials 0.000 description 2
- 239000001301 oxygen Substances 0.000 description 2
- 239000002245 particle Substances 0.000 description 2
- 229910052573 porcelain Inorganic materials 0.000 description 2
- 239000000843 powder Substances 0.000 description 2
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 description 1
- 238000007796 conventional method Methods 0.000 description 1
- 238000005242 forging Methods 0.000 description 1
- 230000004927 fusion Effects 0.000 description 1
- 238000005098 hot rolling Methods 0.000 description 1
- 229910052739 hydrogen Inorganic materials 0.000 description 1
- 239000001257 hydrogen Substances 0.000 description 1
- 239000012535 impurity Substances 0.000 description 1
- 238000004519 manufacturing process Methods 0.000 description 1
- 238000000034 method Methods 0.000 description 1
- 239000011812 mixed powder Substances 0.000 description 1
- 238000002156 mixing Methods 0.000 description 1
- 239000002244 precipitate Substances 0.000 description 1
- VSZWPYCFIRKVQL-UHFFFAOYSA-N selanylidenegallium;selenium Chemical compound [Se].[Se]=[Ga].[Se]=[Ga] VSZWPYCFIRKVQL-UHFFFAOYSA-N 0.000 description 1
- 238000005245 sintering Methods 0.000 description 1
- 239000006104 solid solution Substances 0.000 description 1
- 239000000243 solution Substances 0.000 description 1
Landscapes
- Powder Metallurgy (AREA)
Description
〔発明の技術分野〕
本発明は高温強度が大きく再結晶温度の高いモ
リブデン合金に関する。
〔発明の技術的背景とその問題点〕
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
耐熱材料として使用され、最近では、核融合炉の
炉壁材など原子力分野での用途が広がりつつあ
る。
しかしながら、モリブデン合金は再結晶温度以
上に加熱された後は、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。
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
た、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。
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、一層再結晶温度が高
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。
〔発明の目的〕
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。
〔発明の概要〕
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〜
100ppm、残部がモリブデン(Mo)であることを
特徴とする。
本発明のMo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つて、
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重量%
からあらわれるが、その量が0.5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。好ましくは0.1〜0.2
重量%である。
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100ppm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
まう。好ましくは20〜80ppmである。
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3〜20μmのMo、
Zr、Bの粉末をそれぞれ所定量秤量し、これらを
例えば磁製ポツ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ラバープレスな
どで成形する。この成形体を常法に従つて焼結し
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。
なお、このとき、Mo、Zr、B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つて有用である。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。
かくして得られた合金のインゴツトを熱間鍛
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。
〔発明の実施例〕
(1) 合金の製造
Mo、Zr、B、Cの粉末(平均粒径6μm)
を所定の割合で配合し、これを磁製ポツトロー
ラーで混合した後、3000Kg/cm2の圧でラバープ
レスを用いて成形体とした。
この成形体を1830℃の水素雰囲気中で7時間
焼成し、直径25mm長さ300mmの焼結体とした。
これを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50mm長さ200mmのインゴツト
とした。
得られたMo合金の組成を表に示した。
[Technical Field of the Invention] The present invention relates to a molybdenum alloy with high high temperature strength and high recrystallization temperature. [Technical background of the invention and its problems] Molybdenum alloys have excellent high-temperature stability in vacuum, inert, and reducing atmospheres, so they are used as various heat-resistant materials, and recently, they are used in nuclear fusion reactors. Applications in the nuclear field, such as reactor wall materials, are expanding. However, after a molybdenum alloy is heated above its recrystallization temperature, its ductility at room temperature becomes poor, and brittle fracture easily occurs at grain boundaries, resulting in a decrease in its strength. 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. Also known is an alloy in which a small amount of carbon is added to improve the deoxidizing effect. 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 higher recrystallization temperatures and excellent high-temperature strength. [Object of the Invention] 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. [Summary of the Invention] The molybdenum alloy of the present invention contains 0.02 to 0.5% by weight of zirconium (Zr) and 5 to 5% by weight of boron (B).
100ppm, the balance being molybdenum (Mo). In the Mo alloy of the present invention, Zr forms a solid solution with Mo,
It also combines with oxygen, carbon, etc. in the base metal,
By dispersing it in the base metal,
It is a component that increases the mechanical strength of the alloy, especially its high-temperature strength, and also increases the recrystallization temperature and suppresses coarsening of crystal grains. The effect of Zr is 0.02% by weight
However, if the amount exceeds 0.5% by weight, the rate of increase in recrystallization temperature will decrease and the workability of the obtained alloy will deteriorate. Preferably 0.1-0.2
Weight%. B is a component that greatly contributes to cleaning grain boundaries and prevents coarsening of crystal grains after recrystallization. The effect of this B is that if it is less than 5 ppm, the grain boundary cleaning effect is not sufficient, and if it exceeds 100 ppm,
Mo 2 B precipitates and becomes coarse, making the alloy brittle. Preferably it is 20 to 80 ppm. The Mo alloy of the present invention can be manufactured as follows. That is, Mo with a particle size of 3 to 20 μm,
Predetermined amounts of Zr and B powders are weighed, and after thoroughly mixing them in a mixer such as a porcelain pot mill, the resulting mixed powder is molded using a rubber press or the like. After sintering this molded body according to a conventional method, the obtained sintered body is arc melted in a vacuum to form an alloy. At this time, in addition to Mo, Zr, and B, a small amount of
Preferably, adding carbon in an amount of 300 ppm or less is useful because it further enhances the deoxidizing effect of carbon and the effect of B during arc melting. However, it should be noted that when the amount of residual carbon exceeds 500 ppm, the workability of the alloy deteriorates significantly. 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. [Embodiments of the invention] (1) Production of alloy Mo, Zr, B, C powder (average particle size 6 μm)
were blended in a predetermined ratio, mixed using a porcelain pot roller, and then molded using a rubber press at a pressure of 3000 kg/cm 2 . This molded body was fired in a hydrogen atmosphere at 1830°C for 7 hours to obtain a sintered body with a diameter of 25 mm and a length of 300 mm.
Two of these were joined together and alloyed using the consumable electrode vacuum arc melting method to form an ingot with a diameter of 50 mm and a length of 200 mm. The composition of the obtained Mo alloy is shown in the table.
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耐熱材料としての有用
性に富むものである。
The Mo alloy of the present invention has a high recrystallization temperature,
It also has high high-temperature strength, making it highly useful as a high-temperature heat-resistant material.
第1図は実施例で用いた板材の焼鈍温度とヴイ
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Zr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。
Figure 1 is a diagram showing the relationship between annealing temperature and Witzkars hardness of the plate materials used in the examples, Figure 2 is a diagram showing the relationship between half-softening temperature and Zr content, and Figure 3 is a diagram showing the relationship between annealing temperature and recrystallized grains. FIG. 4 is a diagram showing the relationship between Zr content and recrystallized grain size, and FIG. 5 is a diagram showing the tensile strength at each temperature.
Claims (1)
100ppm、残部がモリブデンからなり、再結晶温
度が高く高温強度が大であることを特徴とするモ
リブデン合金。1 Zirconium 0.02~0.5% by weight, boron 5~
A molybdenum alloy consisting of 100ppm, the balance being molybdenum, and characterized by a high recrystallization temperature and high high-temperature strength.
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 JPS59116356A (en) | 1984-07-05 |
| JPS6221066B2 true 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 (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| CN111164227A (en) * | 2017-09-29 | 2020-05-15 | 普兰西股份有限公司 | Sintered Molybdenum Parts |
Families Citing this family (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| CN102085538B (en) * | 2010-12-24 | 2012-08-22 | 金堆城钼业股份有限公司 | Preparation method of silicon, aluminum, potassium and molybdenum alloy wire |
| 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 |
-
1982
- 1982-12-22 JP JP22401682A patent/JPS59116356A/en active Granted
Cited By (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| CN111164227A (en) * | 2017-09-29 | 2020-05-15 | 普兰西股份有限公司 | Sintered Molybdenum Parts |
| US11925984B2 (en) | 2017-09-29 | 2024-03-12 | Plansee Se | Sintered molybdenum part |
Also Published As
| Publication number | Publication date |
|---|---|
| JPS59116356A (en) | 1984-07-05 |
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