JPH0354802B2 - - Google Patents

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Publication number
JPH0354802B2
JPH0354802B2 JP58071077A JP7107783A JPH0354802B2 JP H0354802 B2 JPH0354802 B2 JP H0354802B2 JP 58071077 A JP58071077 A JP 58071077A JP 7107783 A JP7107783 A JP 7107783A JP H0354802 B2 JPH0354802 B2 JP H0354802B2
Authority
JP
Japan
Prior art keywords
titanium
wire
tungsten
core
evaporation
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 - Lifetime
Application number
JP58071077A
Other languages
Japanese (ja)
Other versions
JPS59196506A (en
Priority date (The priority date 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 date listed.)
Filing date
Publication date
Application filed filed Critical
Priority to JP58071077A priority Critical patent/JPS59196506A/en
Priority to GB08410248A priority patent/GB2142044B/en
Publication of JPS59196506A publication Critical patent/JPS59196506A/en
Publication of JPH0354802B2 publication Critical patent/JPH0354802B2/ja
Granted legal-status Critical Current

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Classifications

    • CCHEMISTRY; METALLURGY
    • C23COATING 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
    • C23CCOATING 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
    • C23C14/00Coating by vacuum evaporation, by sputtering or by ion implantation of the coating forming material
    • C23C14/22Coating by vacuum evaporation, by sputtering or by ion implantation of the coating forming material characterised by the process of coating
    • C23C14/24Vacuum evaporation
    • C23C14/26Vacuum evaporation by resistance or inductive heating of the source
    • YGENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
    • Y02TECHNOLOGIES OR APPLICATIONS FOR MITIGATION OR ADAPTATION AGAINST CLIMATE CHANGE
    • Y02EREDUCTION OF GREENHOUSE GAS [GHG] EMISSIONS, RELATED TO ENERGY GENERATION, TRANSMISSION OR DISTRIBUTION
    • Y02E30/00Energy generation of nuclear origin
    • Y02E30/10Nuclear fusion reactors

Landscapes

  • Chemical & Material Sciences (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Engineering & Computer Science (AREA)
  • Materials Engineering (AREA)
  • Mechanical Engineering (AREA)
  • Metallurgy (AREA)
  • Organic Chemistry (AREA)
  • Non-Insulated Conductors (AREA)
  • Physical Vapour Deposition (AREA)

Description

【発明の詳細な説明】[Detailed description of the invention]

この発明は核融合装置に用いられるチタン蒸発
線に関するものである。 重水素、三重水素など、軽い元素の原子核同志
に衝突させて、核融合反応を起させ、その時に放
出される大きなエネルギーを利用しようとする核
融合装置が開発されつつある。 核融合装置では、真空容器内にプラズマを閉込
み、これを高温に加熱する必要があり、またプラ
ズマが真空容器に直接触れるのを防止するため
に、プラズマに直接面する第一壁は、炭化チタン
(TiC)により被覆する必要がある。 上記炭化チタンは、アセチレンガスなどの炭化
水素ガス雰囲気中で、チタンを加熱し蒸発するこ
とにより得られる。すなわち第一壁表面にて下記
反応 2Ti+C2H2→2TiC+H2 を起させて、炭化チタン膜を第一壁表面に被覆す
るようにしている。チタン源としては、タングス
テン線を芯体とし、その芯体にチタン線を巻線し
たチタン蒸発線が使用されようとしており、第一
壁表面付近に配設された多数本のチタン蒸発線に
直接通電し、それらの融点、沸点等の差を利用し
たチタンを蒸発させることが試みられている。 この場合、チタンの蒸発に要する運転コスト
は、一度に蒸発させるチタン量が多ければ多いほ
ど低減でき、そのためにはチタン装荷量及び蒸発
効果が高くなければならないとされている。 上記従来のチタン蒸発線、即ち、1本のタング
ステン線にチタン線を巻線したものにあつては、
チタン装荷量は0.7g程度が限界とされ、またチ
タン蒸発効果もその20%程度を低く、残の80%が
未蒸発チタンとしては廃棄されており、しかもチ
タンの蒸発途中で断線するなどの欠点があつた。 また一般的にタングステン材料は、約1000℃以
上の熱履歴を一度受けると以後、機械強度がきわ
めて脆弱化するという性質がある。そのため、チ
タンとタングステン芯体のみの組合せのチタン蒸
発線では、使用済みのチタン蒸発線を取り外す等
のために、蒸発線本体に触れると、それだけでタ
ングステン芯体が、破損し脱落してしまい、取り
扱いの上で、実に煩わしいという問題もあつた。 この発明は上記のことから考えられたものであ
つて、タングステン、モリブデン、チタンの再結
晶化、融点、沸点、蒸発の差を利用しているが、
全体的に各物質の重量バランスがよく、高電圧、
高電流、高温に耐え、またチタン蒸発中に断線を
起さず、しかもチタンの装荷量及び蒸発効果など
も高いチタン蒸発線を提供しようとするものであ
る。 またこの発明は、チタン装荷量の増加に伴つて
生ずる溶融チタンの滴下を防止し、チタンの蒸発
効率を更に向上させることができるきわめて経済
性に優れたチタン蒸発線を提供するものである。 上記目的によるこの発明の1つは、複数本のタ
ングステン線を撚線して芯体となし、その芯体に
モリブデン線と複数体のチタン線を巻線してなる
チタン蒸発線にある。 また他の1つの発明は、タングステン撚線に巻
線したモリブデン線及び複数本のチタン線に、所
要間隔を空けて巻線したタングステン線によるガ
ード部材を有するチタン蒸発線にある。 上記構成では、チタン線とともに巻線したモリ
ブデン線が、タングステン芯体により加熱され
て、チタン線を側面からも加熱するようになり、
タングステン芯体のみによる中心部から半径方向
への加熱よりも、チタンの溶融が一様になる。 またチタン線の添え巻き線となるモリブデン線
と、ガード部材となるタングステン線とにより、
溶融チタンは加熱したタングステン芯体に沿つて
均一にぬれるため、局部的な加熱によるタングス
テンの脆弱化も起り難くなる。 この結果、脆弱化によるタングステン芯体の機
械強度劣化が、熱履歴による脆弱化が少ないモリ
ブデン線により補強されることになり、使用済み
のチタン蒸発線の取り扱いがきわめて容易とな
る。 上記芯体となるタングステン線の線径は、0.8
〜1.0φm/mの範囲が好ましく、その2本または
3本を、12〜14m/mの寸法内に3山のピツチに
て撚線してなる。またモリブデン線の線径は、
0.5〜10φm/mの範囲、チタン線は0.8〜1.2φm/
mの範囲がそれぞれ好ましく、それらは12〜
15m/mの寸法にチタン線6山、モリブデン1山
の割合にて巻線され、外径2.8〜2.6φm/mのチ
タン蒸発線を構成する。更にまたガード部材とし
て巻線されるタングステン線の線径は、0.3〜
0.4m/mの範囲でよく、2〜4m/mのピツチに
て巻線される。 次に図示の例によりこの発明を更に詳説す。 図中1はタングステン線、2はモリブデン線、
3はチタン線である。 第1図及び第2図に示す例は、1.0φm/mの2
本のタングステン線1,1を、12m/mの長さl1
範囲に3山の割合で撚線して芯体Aを形成し、そ
の芯体Aの周囲に、0.5φm/mの1本のモリブデ
ン線2と、1.0φm/mの3本のチタン線3,3,
3とを、12m/mの長さl2範囲にモリブデン線2
を含めて7山の割合で巻線し、外径が2.1φm/m
となつたチタン蒸発線を示すものである。 第3図はその正面図を省略したが、上記と同一
線径の3本のタングステン線1,1,1を撚線し
て、芯体Aを形成した場合の縦断面図を示すもの
である。 第4図及び第5図は、第3図と同様に3本のタ
ングステン線1,1,1を撚線した芯体Aに、上
記各例と同様に1本のモリブデン線2と3本のチ
タン線3,3,3とを巻線し、更に0.4φm/mの
タングステン線4を、ガード部材Bとして2m/
mピツチl3にて巻線したチタン蒸発線を示すもの
である。 次に実施例を下記に示す。
This invention relates to a titanium evaporation line used in a nuclear fusion device. Nuclear fusion devices are being developed that attempt to make the nuclei of light elements, such as deuterium and tritium, collide with each other to cause a fusion reaction, and utilize the large amount of energy released at that time. In a nuclear fusion device, it is necessary to confine plasma in a vacuum container and heat it to a high temperature.In order to prevent the plasma from coming into direct contact with the vacuum container, the first wall directly facing the plasma is made of carbonized Must be coated with titanium (TiC). The above-mentioned titanium carbide is obtained by heating and evaporating titanium in a hydrocarbon gas atmosphere such as acetylene gas. That is, the following reaction 2Ti+C 2 H 2 →2TiC+H 2 is caused to occur on the surface of the first wall, so that the titanium carbide film is coated on the surface of the first wall. As a titanium source, a titanium evaporation wire with a tungsten wire as a core and a titanium wire wound around the core is being used. Attempts have been made to evaporate titanium by applying electricity and utilizing the difference in their melting points, boiling points, etc. In this case, the operating cost required for evaporating titanium can be reduced as the amount of titanium evaporated at one time is large, and for this purpose, it is said that the amount of titanium loaded and the evaporation effect must be high. Regarding the conventional titanium evaporation wire mentioned above, that is, one in which a titanium wire is wound around a single tungsten wire,
The amount of titanium loaded is said to be limited to about 0.7g, and the titanium evaporation effect is only about 20% of that amount, and the remaining 80% is discarded as unevaporated titanium, and there are disadvantages such as wire breakage during evaporation of titanium. It was hot. Additionally, in general, tungsten materials have the property that once they have been subjected to a thermal history of approximately 1000°C or higher, their mechanical strength becomes extremely weak. Therefore, with a titanium evaporation wire that has only a combination of titanium and tungsten core, if you touch the evaporation wire to remove a used titanium evaporation wire, the tungsten core will break and fall off. There was also the problem that it was really troublesome to handle. This invention was conceived based on the above, and utilizes the differences in recrystallization, melting point, boiling point, and evaporation of tungsten, molybdenum, and titanium.
Overall, the weight balance of each substance is good, high voltage,
The present invention aims to provide a titanium evaporation wire that can withstand high current and high temperature, does not cause disconnection during titanium evaporation, and has a high titanium loading and evaporation effect. Further, the present invention provides an extremely economical titanium evaporation line that can prevent dripping of molten titanium that occurs with an increase in the amount of titanium loaded, and can further improve titanium evaporation efficiency. One of the inventions according to the above-mentioned object is a titanium evaporated wire formed by twisting a plurality of tungsten wires to form a core, and winding a molybdenum wire and a plurality of titanium wires around the core. Another invention resides in a titanium evaporated wire having a guard member made of a molybdenum wire wound around a tungsten strand and a tungsten wire wound around a plurality of titanium wires at required intervals. In the above configuration, the molybdenum wire wound together with the titanium wire is heated by the tungsten core, and the titanium wire is also heated from the side.
The titanium melts more uniformly than heating radially from the center using only the tungsten core. In addition, molybdenum wire is used as a side winding wire for the titanium wire, and tungsten wire is used as a guard member.
Since the molten titanium uniformly wets the heated tungsten core, the tungsten is less likely to become brittle due to localized heating. As a result, the mechanical strength deterioration of the tungsten core due to weakening is reinforced by the molybdenum wire, which is less susceptible to weakening due to thermal history, making it extremely easy to handle the used titanium evaporation wire. The wire diameter of the tungsten wire that becomes the core above is 0.8
The range is preferably from 1.0 m/m to 1.0 m/m, and two or three of them are twisted at three pitches within a size of 12 to 14 m/m. In addition, the wire diameter of molybdenum wire is
Range of 0.5 to 10φm/m, titanium wire is 0.8 to 1.2φm/
Preferably, m ranges from 12 to
The titanium wire is wound at a ratio of six titanium wires and one molybdenum wire to a size of 15 m/m, forming a titanium evaporation wire with an outer diameter of 2.8 to 2.6 φm/m. Furthermore, the wire diameter of the tungsten wire wound as a guard member is 0.3~
The wire width may be within the range of 0.4 m/m, and the wires are wound at a pitch of 2 to 4 m/m. Next, the present invention will be explained in more detail with reference to illustrated examples. In the figure, 1 is a tungsten wire, 2 is a molybdenum wire,
3 is a titanium wire. The example shown in Fig. 1 and Fig. 2 is 2 mm of 1.0φm/m.
The length of the tungsten wire 1,1 is 12m/m l 1
A core A is formed by twisting the wires at a ratio of three strands in the area, and around the core A, one molybdenum wire 2 of 0.5φm/m and three titanium wires 3 of 1.0φm/m are connected. ,3,
3 and molybdenum wire 2 in a length l 2 range of 12m/m.
The wire is wound at a ratio of 7 threads including the wire, and the outer diameter is 2.1φm/m.
This shows the titanium evaporation line. Although the front view is omitted in Fig. 3, it shows a longitudinal cross-sectional view of the case where the core body A is formed by twisting three tungsten wires 1, 1, 1 with the same wire diameter as above. . Figures 4 and 5 show a core A made up of three twisted tungsten wires 1, 1, 1 as in Figure 3, one molybdenum wire 2 and three twisted wires as in the above examples. Wind the titanium wires 3, 3, 3, and further wind the 0.4φm/m tungsten wire 4 as guard member B.
This figure shows a titanium evaporation wire wound with m pitch l3 . Next, examples are shown below.

【表】 なお、材質の表示に図面中の符号と材質の記号
とを示す。また表中の数字は本数を示す。 上記実施例〜B2は10V、200A程度の電気を
直接通電して加熱したところ、いずれも断線し難
く、チタン蒸発量は最大でチタン装荷量の90%で
あつた。また実施例、ではチタンの水たれ現
象が生じたが、ガード部材Bを巻線した実施例
B1B2B1B2では水滴状たれが発生せず、
チタンの蒸発途中で断線することはなかつた。こ
の結果、チタン装荷量3gが可能となり、その装
荷量の約80%が蒸発した。 比較検討のため、線径0.8〜0.9φm/mのタン
グステン線にチタン線とモリブデン線とを実施例
と同様に巻線したチタン蒸発線を作成し、通電
により蒸発を試みたところ、蒸発中に断線が生
じ、チタン蒸発量はチタン装荷量の1%にも満な
かつた。 したがつて、この発明によるチタン蒸発線は、
従来のものよりもチタン装荷量及びチタン蒸発効
率に優れ、また通電加熱時の断線を防止でき、未
蒸発チタンとして廃棄される量はきわめて少な
く、経済的でもあるなどの特徴を有する。
[Table] In addition, the code in the drawing and the material symbol are shown to indicate the material. Also, the numbers in the table indicate the number of pieces. When the above-mentioned Example ~ B2 was heated by directly applying electricity of about 10 V and 200 A, it was difficult to disconnect, and the amount of titanium evaporated was at most 90% of the amount of titanium loaded. In addition, in the example, a water dripping phenomenon occurred in titanium, but in the example in which the guard member B was wound.
B1 , B2 , B1 , and B2 did not cause water droplet dripping,
There was no disconnection during the evaporation of titanium. As a result, a titanium loading of 3g was possible, and about 80% of the loading was evaporated. For comparative study, a titanium evaporation wire was prepared by winding a titanium wire and a molybdenum wire around a tungsten wire with a wire diameter of 0.8 to 0.9φm/m in the same manner as in the example, and evaporation was attempted by applying electricity. A disconnection occurred and the amount of titanium evaporated was less than 1% of the amount of titanium loaded. Therefore, the titanium evaporation line according to the present invention is
It has the characteristics of being superior in titanium loading and titanium evaporation efficiency than conventional products, being able to prevent disconnection during electrical heating, and being economical as the amount of unevaporated titanium that is discarded is extremely small.

【図面の簡単な説明】[Brief explanation of drawings]

図面はこの発明に係るチタン蒸発線の構成を例
示するもので、第1図は2本のタングステン撚線
を芯体とする場合の一部を切除した正面図、第2
図はその拡大断面図、第3図は3本のタングステ
ン撚線を芯体とするチタン蒸発線の拡大断面図、
第4図はガード部材を巻線したチタン蒸発線の一
部を切除した正面図、第5図はその拡大断面図で
ある。 1,4…タングステン線、2…モリブデン線、
3…チタン線、A…芯体、B…ガード部材。
The drawings illustrate the structure of the titanium evaporation wire according to the present invention.
The figure is an enlarged cross-sectional view, and Figure 3 is an enlarged cross-sectional view of a titanium evaporation wire with three tungsten strands as the core.
FIG. 4 is a partially cutaway front view of the titanium evaporation wire around which the guard member is wound, and FIG. 5 is an enlarged sectional view thereof. 1, 4...Tungsten wire, 2...Molybdenum wire,
3...Titanium wire, A...Core, B...Guard member.

Claims (1)

【特許請求の範囲】 1 複数本のタングステン線を撚線して芯体とな
し、その芯体にモリブデン線と複数本チタン線を
巻線してなることを特徴とするチタン蒸発線。 2 複数本のタングステン撚線からなる芯体と、
その芯体に巻線したモリブデン線及び複数本のチ
タン線と、その巻線の外周に所要間隔を空けて巻
線したタングステン線によるガード部材とからな
ることを特徴とするチタン蒸発線。
[Scope of Claims] 1. A titanium evaporated wire characterized in that a plurality of tungsten wires are twisted to form a core, and a molybdenum wire and a plurality of titanium wires are wound around the core. 2. A core made of multiple stranded tungsten wires,
A titanium evaporation wire characterized by comprising a molybdenum wire and a plurality of titanium wires wound around the core, and a guard member made of tungsten wire wound at a required interval around the outer periphery of the winding.
JP58071077A 1983-04-22 1983-04-22 Titanium evaporated wire Granted JPS59196506A (en)

Priority Applications (2)

Application Number Priority Date Filing Date Title
JP58071077A JPS59196506A (en) 1983-04-22 1983-04-22 Titanium evaporated wire
GB08410248A GB2142044B (en) 1983-04-22 1984-04-19 Titanium evaporation wire

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP58071077A JPS59196506A (en) 1983-04-22 1983-04-22 Titanium evaporated wire

Publications (2)

Publication Number Publication Date
JPS59196506A JPS59196506A (en) 1984-11-07
JPH0354802B2 true JPH0354802B2 (en) 1991-08-21

Family

ID=13450097

Family Applications (1)

Application Number Title Priority Date Filing Date
JP58071077A Granted JPS59196506A (en) 1983-04-22 1983-04-22 Titanium evaporated wire

Country Status (2)

Country Link
JP (1) JPS59196506A (en)
GB (1) GB2142044B (en)

Families Citing this family (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US4925741A (en) * 1989-06-08 1990-05-15 Composite Materials Technology, Inc. Getter wire
GB0320921D0 (en) * 2003-09-06 2003-10-08 Welding Alloys Ltd Wires for manufacturing metallised substrates

Family Cites Families (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
NL253747A (en) * 1959-07-13

Also Published As

Publication number Publication date
GB8410248D0 (en) 1984-05-31
GB2142044B (en) 1986-09-10
GB2142044A (en) 1985-01-09
JPS59196506A (en) 1984-11-07

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