JP3195463B2 - Oxide dispersion strengthened platinum or platinum-rhodium alloy - Google Patents
Oxide dispersion strengthened platinum or platinum-rhodium alloyInfo
- Publication number
- JP3195463B2 JP3195463B2 JP15117493A JP15117493A JP3195463B2 JP 3195463 B2 JP3195463 B2 JP 3195463B2 JP 15117493 A JP15117493 A JP 15117493A JP 15117493 A JP15117493 A JP 15117493A JP 3195463 B2 JP3195463 B2 JP 3195463B2
- Authority
- JP
- Japan
- Prior art keywords
- platinum
- alloy
- oxide dispersion
- oxide
- rhodium alloy
- 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 - Fee Related
Links
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- Powder Metallurgy (AREA)
- Manufacture Of Alloys Or Alloy Compounds (AREA)
Description
【0001】[0001]
【産業上の利用分野】本発明は、ガラス工業等に使用さ
れる白金又は白金−ロジウム合金及びその製造方法に係
り、特に、高温で使用されるガラス溶解装置に用いられ
る高温クリープ特性に優れてかつ伸びのある材料及びそ
の製造方法に関するものである。BACKGROUND OF THE INVENTION 1. Field of the Invention The present invention relates to platinum or a platinum-rhodium alloy used in the glass industry, etc. and a method for producing the same, and more particularly, to an excellent high-temperature creep characteristic used in a glass melting apparatus used at a high temperature. The present invention also relates to a material having elongation and a method for producing the same.
【0002】[0002]
【従来の技術と課題】上記目的用途には従来、Th、Z
r、Y、Hf、Ti、Al等の酸化物を分散させた酸化
物分散強化白金及び白金合金が用いられていたがその高
温でのクリープ強度は必らずしも十分でなく、しかもバ
ラツキの多いものであった。そして、それらの材料はク
リープ破断時の伸びが著しく小さいものであった。2. Description of the Related Art Conventionally, Th, Z
Oxide dispersion strengthened platinum and a platinum alloy in which oxides such as r, Y, Hf, Ti, and Al are dispersed have been used, but their creep strength at high temperatures is not necessarily sufficient, and the dispersion is not uniform. There were many. And those materials had remarkably small elongation at the time of creep rupture.
【0003】[0003]
【発明の目的】本発明は、上記従来の酸化物分散強化白
金又は白金合金よりも高温クリープ特性の優れたもので
あり、伸びが有り、かつ安定した新規な材料を提供する
ものである。An object of the present invention is to provide a novel material which is superior in the high-temperature creep characteristics, has an elongation and is stable in comparison with the conventional oxide dispersion strengthened platinum or platinum alloy.
【0004】[0004]
【発明の構成】上記課題を解決する為に本発明では、高
温で使用されるガラス溶解装置に用いられる酸化物分散
強化白金又は白金−ロジウム合金において、0.05〜
2wt %のSm酸化物が、白金又は白金−ロジウム合金
中に分散されており、高温クリープ特性に優れたことを
特徴とするものとした。 According to the present invention, in order to solve the above problems , a high
Oxide dispersion used in glass melting equipment used at high temperatures
In a reinforced platinum or platinum-rhodium alloy, 0.05 to
2 wt % Sm oxide is platinum or platinum-rhodium alloy
Dispersed inside and has excellent high-temperature creep properties.
The feature was adopted.
【0005】[0005]
【作用】上記のように構成された本発明の酸化物分散強
化白金又は白金−ロジウム合金によれば、Smの酸化物
が白金又は白金−ロジウム合金中に安定に分散されるこ
とにより、従来のZr、Y等の酸化物よりも強く安定し
て転位の移動を妨げることや、また酸化物が結晶の粒界
や粒内に偏在更に層状に偏在することにより、結晶のア
スペクト比が高く保たれることにより高温でのクリープ
強度が強く安定するもので、高温でのクリープ特性が優
れたかつ安定な材料となるものである。特にSmの酸化
物は0.05〜2wt%が有効で、0.05wt%未満
では、その効果が不十分で、また2wt%を超えると加
工が困難となり、工程が嵩み特に光学ガラス溶解時には
溶出によりガラスを汚染する懸念があるものである。ま
た、白金に限らず、白金−ロジウム合金、白金−金合
金、白金−パラジウム合金、白金−パラジウム−ロジウ
ム合金、白金−ロジウム−金合金等の白金合金において
も、同様の作用効果が得られるものである。なお、酸化
物分散強化とは、酸化物が白金または白金合金中に均等
に分散している場合や、結晶粒界または粒内に偏在して
いる場合等も有り、更に層状に偏在している場合等含ま
れるものである。According to the oxide dispersion-strengthened platinum or platinum-rhodium alloy of the present invention constituted as described above, the oxide of Sm is stably dispersed in the platinum or platinum-rhodium alloy, so that the conventional method can be used. The aspect ratio of the crystal was kept high by preventing the movement of dislocations more stably than the oxides of Zr, Y, and the like, and also by the oxide being unevenly distributed in the grain boundaries and in the grains of the crystal and further in the form of a layer. By doing so, the creep strength at high temperatures is strongly stabilized, and the material has excellent and stable creep characteristics at high temperatures. In particular oxides of Sm is valid 0.05~2Wt%, is less than 0.05 wt%, its effect is insufficient, and more than 2 wt% and the processing becomes difficult, when the process is Kasami particularly optical glass melting There is a concern that the glass may be contaminated by dissolution. In addition, not only platinum, but also platinum-rhodium alloy, platinum-gold alloy, platinum-palladium alloy, platinum-palladium-rhodium alloy, platinum-rhodium-gold alloy, and other platinum alloys that can achieve the same function and effect can be obtained. It is. In addition, the oxide dispersion strengthening means that the oxide is uniformly dispersed in platinum or a platinum alloy, or there is a case where the oxide is unevenly distributed in a crystal grain boundary or in a grain, and is further unevenly distributed in a layer shape. Cases are included.
【0006】[0006]
【実施例】以下に実施例、従来例について述べる。ま
ず、実施例1として、Pt(白金)とSm(サマリウ
ム)を溶解鋳造し、PtSm0.3wt%の合金体を得
た。これをアトマイズ法にて溶融噴霧して水中急冷し、
粒径0.01〜0.2mmの粉末を作成した。その後粉
末を大気中(酸素分圧0.2気圧)、温度1250℃、
時間24HにてPtSm合金中のSmを酸化させた後、
粉体をプレスで荷重60〜90kgw/mm2にて圧縮
し、温度1250℃、時間1Hにて焼結熱処理し、更に
再度前記圧縮、焼結熱処理を繰り返し、その後温度12
50℃にて熱間鍛造、次いで冷間圧延し、Smの酸化物
の分散した白金で板厚1mmの試験片を採取した。次ぎ
に、実施例2としてPtとRh(ロジウム)とSmを溶
解、鋳造し、PtRh10wt%Sm0.3wt%の合
金体を得た。その後、実施例1と同一工程にて加工し、
Smの酸化物の分散したPtRh合金で板厚1mmの試
験片を採取した。さらに、実施例3としてPtとSmを
溶解、鋳造し、PtSm0.3wt%の合金体を得た。
その後圧延して板厚0.1mmの板材とした。次いで縦
40mm、横30mmに切断した後、大気中にて温度1
250℃、時間24HにてPtSm合金中のSmを酸化
させた後、プレスで荷重50〜80kgw/mm2にて
圧縮し、次いで温度1250℃、時間1Hにて焼結熱処
理し、更に再度前記圧縮、焼結熱処理を繰り返し、その
後温度1250℃にて熱間鍛造、次いで冷間圧延し、S
mの酸化物の分散した白金で板厚1mmの試験片を採取
した。一方、従来例1として、PtとZr(ジルコニウ
ム)を溶解、鋳造し、PtZr0.3wt%の合金体を
得た。その後実施例1と同じ工程にてZrの酸化物の分
散した白金で板厚1mmの試験片を採取した。また、従
来例2として、PtとY(イットリウム)を溶解、鋳造
し、PtY0.3wt%の合金体を得た。その後実施例
3と同じ工程にてYの酸化物の分散した白金で板厚1m
mの試験片を採取した。然して温度1400℃、荷重
1.5kgw/mm2の荷重に対する破断時間に対する
評価結果を以下に示す。Embodiments and conventional examples will be described below. First, as Example 1, Pt (platinum) and Sm (samarium )
Arm) was dissolved cast, to give a PtSm0.3Wt% of the alloy body. This is melt-sprayed by the atomizing method and quenched in water,
A powder having a particle size of 0.01 to 0.2 mm was prepared. Thereafter, the powder was placed in the atmosphere (oxygen partial pressure 0.2 atm), temperature 1250 ° C,
After oxidizing Sm in the PtSm alloy at time 24H,
The powder is compressed by a press under a load of 60 to 90 kgw / mm 2 , and subjected to a sintering heat treatment at a temperature of 1250 ° C. for 1 hour, and the above-described compression and sintering heat treatment is repeated again.
Hot forging was performed at 50 ° C., and then cold-rolled, and a 1-mm-thick test piece was collected from platinum in which Sm oxide was dispersed. Next, as Example 2, Pt, Rh (rhodium) and Sm were melted and cast to obtain an alloy body of 10 wt% PtRh and 0.3 wt% of Sm. Then, processing is performed in the same process as in Example 1,
A 1 mm-thick test piece was sampled from a PtRh alloy in which Sm oxide was dispersed. Further, as Example 3, Pt and Sm were melted and cast to obtain an alloy body of 0.3 wt% of PtSm.
Thereafter, it was rolled to obtain a plate material having a plate thickness of 0.1 mm. Next, after cutting into a length of 40 mm and a width of 30 mm, the temperature was reduced to 1 in air.
After oxidizing Sm in the PtSm alloy at 250 ° C. for 24 hours, it was compressed with a press at a load of 50 to 80 kgw / mm 2 , then subjected to a sintering heat treatment at a temperature of 1250 ° C. for 1 hour, and then compressed again. , Sintering heat treatment is repeated, then hot forging at a temperature of 1250 ° C., then cold rolling,
A test piece having a plate thickness of 1 mm was collected from platinum in which m oxides were dispersed. On the other hand, as Conventional Example 1, Pt and Zr ( zirconium
Beam) dissolved, and cast to obtain a PtZr0.3Wt% of the alloy body. Thereafter, in the same process as in Example 1, a test piece having a thickness of 1 mm was sampled from platinum in which Zr oxide was dispersed. Further, as Conventional Example 2, Pt and Y (yttrium) were melted and cast to obtain an alloy body of 0.3 wt% PtY. Later example
In the same process as in Step 3 , plate thickness of 1 m
m test pieces were collected. However, the evaluation results for the rupture time at a temperature of 1400 ° C. and a load of 1.5 kgw / mm 2 are shown below.
【0007】[0007]
【表1】 [Table 1]
【0008】[0008]
【発明の効果】以上のように本発明の酸化物分散強化白
金又は白金−ロジウム合金によれば、Sm酸化物が白金
又は白金−ロジウム合金中に安定に分散されることによ
り、転移の移動を強く妨げることとなり、高温でのクリ
ープ強度が強く安定した優れてかつ伸びのある材料が得
られるものである。As described above, according to the oxide dispersion-strengthened platinum or platinum-rhodium alloy of the present invention, Sm oxide is stably dispersed in platinum or a platinum-rhodium alloy, so that the transfer of transition can be prevented. An excellent and elongate material having strong and stable creep strength at a high temperature can be obtained.
フロントページの続き (51)Int.Cl.7 識別記号 FI C22C 1/04 C22C 1/04 E // C22C 1/10 1/10 B 32/00 32/00 Z (56)参考文献 特開 平3−188231(JP,A) 特公 昭29−2604(JP,B1) He,Huachun;Hu,Cha ngyi;Guo Jinxin;Ch en Fushang”Effects of rare earth ele ments on high−temp aratures tensile s trength and ductiv itt of platinum”Gu ijinshu(1991)12(2)19−24 岡田、後藤”白金族と工業的利用" P.222 産業図書株式会社 昭和31年 12月20日発行 (58)調査した分野(Int.Cl.7,DB名) C22C 1/04 - 1/10 C22C 5/04 B22F 1/00 - 9/30 Continuation of the front page (51) Int.Cl. 7 Identification symbol FI C22C 1/04 C22C 1/04 E // C22C 1/10 1/10 B 32/00 32/00 Z (56) References JP-A-3 -188231 (JP, A) Japanese Patent Publication No. 29-2604 (JP, B1) He, Huachun; Hu, Changyi; Guo Jinxin; Itt of Platinum, "Guijinshu (1991) 12 (2) 19-24 Okada, Goto," Platinum family and industrial use. " 222 Sangyo Tosho Co., Ltd. Published on December 20, 1956 (58) Field surveyed (Int.Cl. 7 , DB name) C22C 1/04-1/10 C22C 5/04 B22F 1/00-9/30
Claims (1)
られる酸化物分散強化白金又は白金−ロジウム合金にお
いて、 0.05〜2wt%のSm酸化物が、白金又は白金−ロ
ジウム合金中に分散されており、高温クリープ特性に優
れたことを特徴とする酸化物分散強化白金又は白金−ロ
ジウム合金。1. An oxide dispersion-strengthened platinum or platinum-rhodium alloy used in a glass melting apparatus used at a high temperature, wherein 0.05 to 2 wt% of Sm oxide is platinum or platinum-rhodium .
Oxide dispersion-strengthened platinum or platinum- alloy characterized by having excellent high-temperature creep characteristics dispersed in a lithium alloy .
Indium alloy.
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP15117493A JP3195463B2 (en) | 1993-05-28 | 1993-05-28 | Oxide dispersion strengthened platinum or platinum-rhodium alloy |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP15117493A JP3195463B2 (en) | 1993-05-28 | 1993-05-28 | Oxide dispersion strengthened platinum or platinum-rhodium alloy |
Publications (2)
Publication Number | Publication Date |
---|---|
JPH06336631A JPH06336631A (en) | 1994-12-06 |
JP3195463B2 true JP3195463B2 (en) | 2001-08-06 |
Family
ID=15512930
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
JP15117493A Expired - Fee Related JP3195463B2 (en) | 1993-05-28 | 1993-05-28 | Oxide dispersion strengthened platinum or platinum-rhodium alloy |
Country Status (1)
Country | Link |
---|---|
JP (1) | JP3195463B2 (en) |
Cited By (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JP2008266031A (en) * | 2007-04-16 | 2008-11-06 | Ohara Inc | Method for producing optical glass |
Families Citing this family (5)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JP3666289B2 (en) | 1998-05-20 | 2005-06-29 | 株式会社デンソー | Thermistor type temperature sensor |
EP1380660B1 (en) | 2001-04-13 | 2006-06-14 | Tanaka Kikinzoku Kogyo K.K. | Method for preparing reinforced platinum material |
RU2333974C2 (en) * | 2004-10-08 | 2008-09-20 | Танака Кикинзоку Когио К.К. | Platinum material, strengthened by disperse oxide particle |
KR101279555B1 (en) * | 2011-03-24 | 2013-06-28 | 희성금속 주식회사 | Method of manufacturing an oxide dispersion strengthened Platinum materials using a Cross-roll |
KR101419443B1 (en) * | 2012-03-26 | 2014-07-14 | 희성금속 주식회사 | Method of an oxide dispersion strengthened platinum-gold alloy |
-
1993
- 1993-05-28 JP JP15117493A patent/JP3195463B2/en not_active Expired - Fee Related
Non-Patent Citations (2)
Title |
---|
He,Huachun;Hu,Changyi;Guo Jinxin;Chen Fushang"Effects of rare earth elements on high−temparatures tensile strength and ductivitt of platinum"Guijinshu(1991)12(2)19−24 |
岡田、後藤"白金族と工業的利用"P.222 産業図書株式会社 昭和31年12月20日発行 |
Cited By (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JP2008266031A (en) * | 2007-04-16 | 2008-11-06 | Ohara Inc | Method for producing optical glass |
Also Published As
Publication number | Publication date |
---|---|
JPH06336631A (en) | 1994-12-06 |
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