JPS60200978A - Clad vessel - Google Patents
Clad vesselInfo
- Publication number
- JPS60200978A JPS60200978A JP5772384A JP5772384A JPS60200978A JP S60200978 A JPS60200978 A JP S60200978A JP 5772384 A JP5772384 A JP 5772384A JP 5772384 A JP5772384 A JP 5772384A JP S60200978 A JPS60200978 A JP S60200978A
- Authority
- JP
- Japan
- Prior art keywords
- vessel
- alloy
- life
- crucible
- container
- 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
Classifications
-
- F—MECHANICAL ENGINEERING; LIGHTING; HEATING; WEAPONS; BLASTING
- F27—FURNACES; KILNS; OVENS; RETORTS
- F27B—FURNACES, KILNS, OVENS OR RETORTS IN GENERAL; OPEN SINTERING OR LIKE APPARATUS
- F27B14/00—Crucible or pot furnaces
- F27B14/08—Details specially adapted for crucible or pot furnaces
- F27B14/10—Crucibles
-
- C—CHEMISTRY; METALLURGY
- C03—GLASS; MINERAL OR SLAG WOOL
- C03B—MANUFACTURE, SHAPING, OR SUPPLEMENTARY PROCESSES
- C03B5/00—Melting in furnaces; Furnaces so far as specially adapted for glass manufacture
- C03B5/06—Melting in furnaces; Furnaces so far as specially adapted for glass manufacture in pot furnaces
- C03B5/08—Glass-melting pots
-
- C—CHEMISTRY; METALLURGY
- C23—COATING METALLIC MATERIAL; COATING MATERIAL WITH METALLIC MATERIAL; CHEMICAL SURFACE TREATMENT; DIFFUSION TREATMENT OF METALLIC MATERIAL; COATING BY VACUUM EVAPORATION, BY SPUTTERING, BY ION IMPLANTATION OR BY CHEMICAL VAPOUR DEPOSITION, IN GENERAL; INHIBITING CORROSION OF METALLIC MATERIAL OR INCRUSTATION IN GENERAL
- C23C—COATING METALLIC MATERIAL; COATING MATERIAL WITH METALLIC MATERIAL; SURFACE TREATMENT OF METALLIC MATERIAL BY DIFFUSION INTO THE SURFACE, BY CHEMICAL CONVERSION OR SUBSTITUTION; COATING BY VACUUM EVAPORATION, BY SPUTTERING, BY ION IMPLANTATION OR BY CHEMICAL VAPOUR DEPOSITION, IN GENERAL
- C23C30/00—Coating with metallic material characterised only by the composition of the metallic material, i.e. not characterised by the coating process
Landscapes
- Chemical & Material Sciences (AREA)
- Engineering & Computer Science (AREA)
- Materials Engineering (AREA)
- Mechanical Engineering (AREA)
- Organic Chemistry (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Metallurgy (AREA)
- General Engineering & Computer Science (AREA)
- Glass Melting And Manufacturing (AREA)
- Physical Vapour Deposition (AREA)
- Other Surface Treatments For Metallic Materials (AREA)
- Crucibles And Fluidized-Bed Furnaces (AREA)
Abstract
Description
【発明の詳細な説明】 本発明は、クラッド容器に関するものである。[Detailed description of the invention] TECHNICAL FIELD The present invention relates to a clad container.
従来、′「a又はT a合金の容器は高温カラスや金属
酸化物を含む鉱石溶解用るつほや真空蒸着用のトレー、
ポー1−なとに広く用いられていた。これは、’1−
aの融点か約3000 ’Cと非當に高く、延性展性に
冨むため容易に加工てきるからである。ところか、1゛
aは400°Cをこえると空気中の酸素と反応して酸化
物を作りやすいため不活性雰囲気で使用しなければなら
ないというわずられしさかあった。さらに、このような
不活性雰囲気中で使用しても、金属酸化物を含むカラス
や鉱石なとをl容)Wする場合には、l容器、4J!物
の中に含まれる酸素とT aが結合して酸化物を作り、
容器の1゛aか溶出して容器の寿命が短かいという欠点
かあった。このため他の金属を加えて合金とし耐消耗性
の向上か図られているが、′1゛aの酸化を防止するに
足る合金が発見されていないのか実情である。Conventionally, containers for ``a'' or Ta alloys have been used for high-temperature glass, melting holes for ores containing metal oxides, trays for vacuum evaporation,
It was widely used in po-1-nato. This is '1-
This is because the melting point of a is extremely high at about 3000'C, and it is ductile and malleable, so it can be easily processed. On the other hand, 1゛a tends to react with oxygen in the air and form oxides when the temperature exceeds 400°C, so it had to be used in an inert atmosphere, which was a hassle. Furthermore, even if used in such an inert atmosphere, if you want to store crows or ores containing metal oxides in a 1 volume container, 4J! Oxygen contained in substances and Ta combine to form oxides,
The disadvantage was that 1゛a of the container was eluted and the life of the container was short. For this reason, attempts have been made to improve wear resistance by adding other metals to the alloy, but the reality is that no alloy sufficient to prevent the oxidation of '1'a has yet been discovered.
本発明は上記欠点に漏みなされたものであり、耐消耗性
の優れた長寿命の容器を提供することを目的とする。The present invention has been made in view of the above-mentioned drawbacks, and an object of the present invention is to provide a long-life container with excellent wear resistance.
本発明は、T a又は′Fa合金の表面にRh又はRh
合金が被覆されていることを特徴とするクラッド容器で
ある。The present invention provides Rh or Rh on the surface of Ta or 'Fa alloy.
This is a clad container characterized by being coated with an alloy.
本発明において、l々h又はRh合金を用いるのは、R
hの融点か1960°Cと′1゛aと同様に高く、しか
も600℃をこえれば酸素と反応して酸化するものの1
100℃では分解し耐酸化性特に金属酸化物に対する耐
酸化性に優れているからである。しかし、無垢のRhや
Rh合金の容器は高価で加工か困藤なため被覆すること
とした。被覆はイオンブレーティングやスパツタリング
や蒸着なとの物理的蒸着が湿式蒸着よりも良い。これは
、物理的蒸着によれば゛pa容器の表面層にRh原子が
埋没されて’l’ aとHk+の接合面の密着強度か1
°bくなり、(浅域的強度。高いクラット容器が得られ
るからである。In the present invention, the use of lh or Rh alloy means that R
The melting point of h is 1960°C, which is as high as '1'a, and if it exceeds 600°C, it will react with oxygen and oxidize.
This is because it decomposes at 100°C and has excellent oxidation resistance, particularly against metal oxides. However, containers made of solid Rh or Rh alloy are expensive and difficult to process, so we decided to cover them. Physical vapor deposition such as ion blasting, sputtering, or vapor deposition is better than wet vapor deposition for coating. According to physical vapor deposition, Rh atoms are buried in the surface layer of the 'pa container, and the adhesion strength of the bonding surface between 'l'a and Hk+ is increased by 1.
°b (shallow area strength).This is because a high crack container can be obtained.
このように、Rh又はRh合金を被覆したるつばは耐酸
化性に優れ、接合面の機械的強度も優れていることから
長寿命のものとなる。なお、Rh合金としては、pt−
Rh、1r−Rhがある。As described above, the crucible coated with Rh or Rh alloy has excellent oxidation resistance and excellent mechanical strength of the joint surface, so it has a long life. In addition, as the Rh alloy, pt-
There are Rh and 1r-Rh.
以下、実施例と従来例について説明する。Examples and conventional examples will be described below.
〔実施例1〕
肉厚5im、II石さ 100mm 、内径80mmの
断面コの字形’I” a Mるつぼの内壁に次の条件で
Rhを厚さ10μmまでイオンブレーティングした。[Example 1] Rh was ion-blasted to a thickness of 10 μm on the inner wall of a U-shaped cross-sectional 'I'' a M crucible having a wall thickness of 5 mm, a II stone size of 100 mm, and an inner diameter of 80 mm under the following conditions.
雰囲気ガス: 2.0X10 mll11gイオン化電
圧、電流:40V、5A
電子ビ−ムン容解: 9 k v、 300 +nA熱
電子 : IOV、1oOA
これを実用品1とする。Atmospheric gas: 2.0 x 10 ml, 11 g Ionization voltage, current: 40 V, 5 A Electron beam solubility: 9 kV, 300 +nA Thermal electron: IOV, 1oOA This is designated as Practical Product 1.
〔実施例2〕
実施例1と同一形状のT aMるつぼの内外壁に次の条
件でI) L −Rh合金を厚さ 0.1mmマグネト
ロンスパッタリンクした。[Example 2] I) L-Rh alloy was magnetron sputter-linked to a thickness of 0.1 mm on the inner and outer walls of a TaM crucible having the same shape as in Example 1 under the following conditions.
圧力ニArガス3 X iOmm l1g印加亀圧:
400V
高周波電源: 13.56 Mllz
これを実用品2とする。Pressure: Ar gas 3 X iOmm l1g applied tortoise pressure:
400V high frequency power supply: 13.56 Mllz This is considered as practical product 2.
実施例1で用いた′r a Mるつぼを従来品とした。 The 'raM crucible used in Example 1 was made into a conventional product.
次に、上記実用品1,2と従来品にアルカリ亜鉛硼珪酸
ガラスを500 g入れAr雰囲気、温度約1200℃
×60分間で使用した。これを10回くり返したところ
、従来品は50μmその′1゛a容器の表面から削られ
たのに対し、実用品1ば10μm、実用品2は5μm削
られたにととまった。Next, 500 g of alkali zinc borosilicate glass was added to the above practical products 1 and 2 and the conventional product in an Ar atmosphere at a temperature of about 1200°C.
It was used for 60 minutes. When this process was repeated 10 times, 50 μm of the conventional product was removed from the surface of the container, while 10 μm of practical product 1 and 5 μm of practical product 2 were removed.
次に、実用品2と従来例の容器の底部を大気中で直接ヒ
ーター加熱して温度約1000°Cで10時間保持した
ところ、従来例ばTaが殆んど酸化されたのに対し、実
用品2ば殆んと酸化されなかった。Next, when the bottoms of the containers of Practical Product 2 and the conventional example were directly heated with a heater in the air and held at a temperature of about 1000°C for 10 hours, most of the Ta in the conventional example was oxidized, but the actual Product 2 was hardly oxidized.
なお、従来品の表面層の硬度と実用品1.2の境界層の
硬度はそれぞれ10011v、160Hv、13011
vでであった。The hardness of the surface layer of the conventional product and the hardness of the boundary layer of the practical product 1.2 are 10011v, 160Hv, and 13011V, respectively.
It was in v.
これらのことから本発明のクラットるつほは従来品に比
べて金属酸化物の溶解用るつぼとして著しく耐酸化性が
優れ、しかも外壁までRh合金被覆した実用品2は大気
加熱しても耐酸化性か優れていることかわかる。また、
実用品の境界層の硬度は従来品の表面層の硬度より高い
ことから、実用品は機械的強度に優れていることがわか
る。From these facts, the crucible of the present invention has significantly superior oxidation resistance as a crucible for dissolving metal oxides compared to conventional products, and Practical Product 2, which is coated with Rh alloy up to the outer wall, is oxidation resistant even when heated in the atmosphere. You can tell whether it's sex or superiority. Also,
The hardness of the boundary layer of the practical product is higher than that of the surface layer of the conventional product, which indicates that the practical product has excellent mechanical strength.
以上詳述したように本発明によれは、耐消耗性の優れた
し寿命のクラッド容器を提供することができる。しかも
、′1゛a製容器を完全に被覆すれば大気中でも長寿命
のものかえられ、j口Jhlliな設Ojηを必要とせ
ず、高価なRhか少星ですむことと併せて安価なものと
なる。As described in detail above, the present invention can provide a clad container with excellent wear resistance and long life. Moreover, if the container made of '1゛a is completely coated, it can be replaced with a long-life one even in the atmosphere, does not require extensive installation, and can be done with expensive Rh or small stars. Become.
出願人 田中貴金属工業株式会社Applicant Tanaka Kikinzoku Kogyo Co., Ltd.
Claims (1)
合金を被覆されていることを特徴と3−るクラット容器
。'] 17h or 1211 on the surface of 'd or '1a alloy
3. A crat container characterized by being coated with an alloy.
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP5772384A JPS60200978A (en) | 1984-03-26 | 1984-03-26 | Clad vessel |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP5772384A JPS60200978A (en) | 1984-03-26 | 1984-03-26 | Clad vessel |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| JPS60200978A true JPS60200978A (en) | 1985-10-11 |
| JPH0317069B2 JPH0317069B2 (en) | 1991-03-07 |
Family
ID=13063856
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP5772384A Granted JPS60200978A (en) | 1984-03-26 | 1984-03-26 | Clad vessel |
Country Status (1)
| Country | Link |
|---|---|
| JP (1) | JPS60200978A (en) |
Cited By (3)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JPH01132751A (en) * | 1987-11-17 | 1989-05-25 | Tanaka Kikinzoku Kogyo Kk | Clad vessel |
| JPH01275779A (en) * | 1988-04-28 | 1989-11-06 | Tanaka Kikinzoku Kogyo Kk | clad container |
| JPH01279777A (en) * | 1988-04-28 | 1989-11-10 | Tanaka Kikinzoku Kogyo Kk | Clad vessel |
-
1984
- 1984-03-26 JP JP5772384A patent/JPS60200978A/en active Granted
Cited By (3)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JPH01132751A (en) * | 1987-11-17 | 1989-05-25 | Tanaka Kikinzoku Kogyo Kk | Clad vessel |
| JPH01275779A (en) * | 1988-04-28 | 1989-11-06 | Tanaka Kikinzoku Kogyo Kk | clad container |
| JPH01279777A (en) * | 1988-04-28 | 1989-11-10 | Tanaka Kikinzoku Kogyo Kk | Clad vessel |
Also Published As
| Publication number | Publication date |
|---|---|
| JPH0317069B2 (en) | 1991-03-07 |
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