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JPH0338946B2 - - Google Patents
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JPH0338946B2 - - Google Patents

Info

Publication number
JPH0338946B2
JPH0338946B2 JP60184760A JP18476085A JPH0338946B2 JP H0338946 B2 JPH0338946 B2 JP H0338946B2 JP 60184760 A JP60184760 A JP 60184760A JP 18476085 A JP18476085 A JP 18476085A JP H0338946 B2 JPH0338946 B2 JP H0338946B2
Authority
JP
Japan
Prior art keywords
pure
alloy
brazing
brazed
weight
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
JP60184760A
Other languages
Japanese (ja)
Other versions
JPS6245467A (en
Inventor
Akira Mori
Masaki Morikawa
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
Mitsubishi Materials Corp
Original Assignee
Mitsubishi Materials Corp
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 by Mitsubishi Materials Corp filed Critical Mitsubishi Materials Corp
Priority to JP60184760A priority Critical patent/JPS6245467A/en
Publication of JPS6245467A publication Critical patent/JPS6245467A/en
Publication of JPH0338946B2 publication Critical patent/JPH0338946B2/ja
Granted legal-status Critical Current

Links

Description

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

〔産業上の利用分野〕 この発明は、軽量にして、冷却効果が高く、例
えば炭酸ガスレーザーの反射鏡や、真空炉の内壁
材などとして用いるのに適した複合ろう付け部材
の製造法に関するものである。 〔従来の技術〕 従来、一般に、例えば炭酸ガスの反射鏡とし
て、純Cu製表面を鏡面仕上げしたものや、さら
にこの表面にAuめつきを施したものなどが用い
られている。 しかしながら、これらのCu製反射鏡では、レ
ーザー照射時間が長くなると、鏡面に加工材から
発生した金属や非金属の蒸気が蒸着し、その反射
率が低下するようになるばかりでなく、鏡面がレ
ーザーのエネルギーを吸収して溶融し、反射鏡を
破損してしまうなどの事故が発生している。 このような事故を防止するには、定期的に鏡面
の蒸着物を除去しなければならないが、反射鏡を
構成する純CuやAuめつきは非常に軟らかいため
に、ふき取るときに鏡面を傷つけ易く、反射特性
を損うことが多発していた。 このようなことから、近年、炭酸ガスレーザー
の反射鏡の材料として、純Cuに代つて硬質のMo
を使用することが定着しつつある。このMo製反
射鏡としては、特に単結晶のものや、微細な結晶
粒の多結晶のものが蒸発物の付着も少なく、すぐ
れた性能を発揮するものである。 〔発明が解決しようとする問題点〕 一方、炭酸ガスレーザー装置は、地上設備ばか
りでなく、宇宙ステーシヨンにも設置されるもの
であるため、装置自体の軽量化が要求されるよう
になつており、これに伴つて、比重の大きい(重
質の)Mo製反射鏡の重量軽減が強く望まれてい
る。 〔問題点を解決するための手段〕 そこで、本発明者等は、上述のような観点か
ら、Mo製反射鏡などのMo部材や、Mo合金部
材、さらに同様に重質のW部材やW合金部材に着
目し、これの軽量化をはかるべく研究を行なつた
結果、純Mo、Mo合金、純W、およびW合金の
うちのいずれかからなる部材の一部を軽量の(比
重の小さい)純AlまたはAl合金で構成し、一方、
例えば純Moと純Alは、比重(純Mo:10.2、純
Al:2.7)、熱膨張率(純Mo:5×10-6/℃、純
Al:23.3×10-6/℃)、および熱伝導率(純Mo:
0.35cal/cm−s−℃、純Al:0.53cal/cm−s−
℃)など種々の点で特性上著しく異なるので、こ
れら両部材を高い接合強度でろう付けすることは
きわめて困難であるが、上記の純Mo、Mo合金、
純W、およびW合金のうちのいずれかからなる部
材のろう付け面に、予め、箔体の溶着あるいは溶
融めつきなどの手段によつて、Si:3〜14重量%
を含有するAl合金のろう材層を固着形成してお
き、この状態で純AlまたはAl合金部材のろう付
け面と重ね合わせ、前記ろう材層を介して真空ろ
う付けを行なうと、高い接合強度でのろう付けが
可能となるという知見を得たのである。 この発明は、上記知見にもとづいてなされたも
ので、純Mo、Mo合金、純W、およびW合金の
うちのいずれかからなる被ろう付け部材のろう付
け面に、Si:3〜14重量%を含有するAl合金で
構成された平均層厚:0.1〜1mmのろう材層を固
着形成しておき、この被ろう付け部材を、前記ろ
う材層を介して、純AlまたはAl合金からなる基
体に真空ろう付けすることからなる複合ろう付け
部材の製造法に特徴を有するものである。 なお、この発明の方法において、ろう材のSi含
有量を3〜14重量%と限定したのは、その含有量
が3重量%未満では、ろう材の融点が660℃を越
えて高くなりすぎ、基体の融点より高いろう付け
温度を必要とする場合が生じるようになつて、ろ
う付け温度を必要とする場合が生じるようになつ
て、ろう付けが不可能となる場合が生じ、一方そ
の含有量が14重量%を越えても、ろう材の融点が
660℃を越えるようになる場合が生ずるようにな
るばかりでなく、被ろう付け部材との反応が著し
くなつてエロージヨンを起すようになることか
ら、その含有量を3〜14重量%と定めたのであ
る。また、同じくろう材層の平均層厚を0.1〜1
mmとしたのは、その平均層厚が0.1mm未満では、
所望の強固な接合強度を確保することができず、
一方その平均層厚が1mmを越えると、ろう材がろ
う付け面からはみ出し、後処理がめんどうになる
という理由によるものである。 〔実施例〕 つぎに、この発明の方法を実施例により説明す
る。 被ろう付け部材として、それぞれ第1表に示さ
れる組成を有し、かつ直径:100mm×厚さ:2mm
の寸法をもつた部材を用意し、この被ろう付け部
材の片側面に、予め、第1表に示される組成およ
び平均層厚を有するろう材層を同じく第1表に示
される公知の手段、すなわち溶着はろう材を被ろ
う付け部材の片側面に載置し、1×10-4torrの真
空中、温度:700℃に加熱の条件、また溶融めつ
きは温度:700℃に保持した溶融ろう材中に浸漬
の条件にて固着形成し、ついで、この被ろう付け
部材を、同じく第1表に示される組成を有し、か
つ直径:100mm×厚さ:20mmの寸法を有する基体
の上面に、前記ろう材層を介して重ね合わせ、こ
の上に5Kgの重りを乗せた状態で、圧力:1×
10-5torrの真空中、600〜630℃の範囲内の温度に
15分間保持の条件で真空ろう付けを行ない、複合
ろう付け部材を製造することによつて本発明法1
〜8をそれぞれ実施した。 つぎに、この結果得られた複合ろう付け部材か
ら試片を切り出し、接合面の引張強さを測定した
ところ、第1表に示される結果を示した。
[Industrial Application Field] This invention relates to a method for manufacturing a composite brazed member that is lightweight, has a high cooling effect, and is suitable for use as, for example, a reflector for a carbon dioxide laser or an inner wall material for a vacuum furnace. It is. [Prior Art] Conventionally, for example, as a carbon dioxide gas reflecting mirror, a mirror-finished pure Cu surface or a mirror-finished surface, or a mirror plated with Au plating, etc., have been used. However, with these Cu reflectors, when the laser irradiation time becomes long, metal and non-metal vapors generated from the processed materials are deposited on the mirror surface, which not only reduces the reflectance, but also causes the mirror surface to be exposed to the laser. Accidents have occurred in which the mirror absorbs energy and melts, damaging the reflector. To prevent such accidents, it is necessary to regularly remove deposits from the mirror surface, but since the pure Cu and Au plating that makes up the reflective mirror is very soft, it is easy to damage the mirror surface when wiping it off. , the reflective properties were frequently impaired. For this reason, in recent years, hard Mo has been used as a material for carbon dioxide laser reflectors instead of pure Cu.
The use of . As for this Mo reflector, single-crystal ones and polycrystal ones with fine crystal grains exhibit excellent performance with less adhesion of evaporated matter. [Problems to be solved by the invention] On the other hand, since carbon dioxide laser devices are installed not only in ground equipment but also in space stations, there is a growing demand for the device itself to be lightweight. , Along with this, there is a strong desire to reduce the weight of Mo reflectors that have a high specific gravity (heavy). [Means for Solving the Problems] Therefore, from the above-mentioned viewpoint, the present inventors developed Mo members such as Mo reflectors, Mo alloy members, and similar heavy W members and W alloys. As a result of focusing on components and conducting research to reduce their weight, we found that some components made of pure Mo, Mo alloy, pure W, and W alloy were made lighter (lower specific gravity). Composed of pure Al or Al alloy, while
For example, the specific gravity of pure Mo and pure Al (pure Mo: 10.2, pure
Al: 2.7), thermal expansion coefficient (pure Mo: 5×10 -6 /℃, pure
Al: 23.3×10 -6 /℃), and thermal conductivity (pure Mo:
0.35cal/cm-s-℃, pure Al: 0.53cal/cm-s-
It is extremely difficult to braze these two parts with high bonding strength because their properties differ significantly in various respects such as
Si: 3 to 14% by weight is preliminarily applied to the brazing surface of a member made of pure W or W alloy by means such as welding a foil or melt plating.
If a brazing material layer of an Al alloy containing Al alloy is firmly formed, and in this state it is overlapped with the brazing surface of a pure Al or Al alloy member, and vacuum brazing is performed through the brazing material layer, high bonding strength can be achieved. They obtained the knowledge that it is possible to perform brazing. This invention was made based on the above knowledge, and the brazing surface of a member to be brazed made of pure Mo, Mo alloy, pure W, or W alloy contains 3 to 14% by weight of Si. A brazing material layer having an average layer thickness of 0.1 to 1 mm is fixedly formed, and the brazing member is then bonded to a substrate made of pure Al or an Al alloy through the brazing material layer. This method is characterized by a method of manufacturing a composite brazed member, which comprises vacuum brazing the parts. In the method of this invention, the Si content of the brazing filler metal is limited to 3 to 14% by weight because if the content is less than 3% by weight, the melting point of the brazing filler metal will exceed 660°C, which is too high. There are cases in which a brazing temperature higher than the melting point of the substrate is required; Even if the amount exceeds 14% by weight, the melting point of the filler metal
The content was set at 3 to 14% by weight because not only would the temperature exceed 660℃, but also the reaction with the parts to be brazed would become significant and cause erosion. be. Also, the average layer thickness of the filler metal layer was set to 0.1 to 1.
mm is used because if the average layer thickness is less than 0.1 mm,
Unable to secure the desired strong joint strength,
On the other hand, if the average layer thickness exceeds 1 mm, the brazing filler metal protrudes from the brazing surface, making post-treatment troublesome. [Example] Next, the method of the present invention will be explained with reference to an example. Each member to be brazed has the composition shown in Table 1, and diameter: 100 mm x thickness: 2 mm.
A member having the dimensions is prepared, and a brazing material layer having the composition and average layer thickness shown in Table 1 is preliminarily applied to one side of the member to be brazed using the known means shown in Table 1. In other words, welding is performed by placing the brazing material on one side of the component to be brazed and heating it to a temperature of 700°C in a vacuum of 1 The member to be brazed is fixedly formed by immersion in the brazing material, and then the member to be brazed is placed on the upper surface of a base having the composition shown in Table 1 and having dimensions of diameter: 100 mm x thickness: 20 mm. were stacked on top of each other through the brazing material layer, and a 5 kg weight was placed on top of the brazing material layer, and the pressure was 1×.
At a temperature within the range of 600-630°C in a vacuum of 10 -5 torr
The method 1 of the present invention is carried out by performing vacuum brazing under the condition of holding for 15 minutes and manufacturing a composite brazed member.
- 8 were carried out, respectively. Next, a specimen was cut out from the composite brazed member obtained as a result, and the tensile strength of the joint surface was measured, and the results shown in Table 1 were obtained.

〔発明の効果〕〔Effect of the invention〕

第1表に示される結果から、本発明法1〜8に
おいては、いずれも従来ろう付け接合がきわめて
困難であるとされていた純Mo、Mo合金、純W、
およびW合金のうちのいずれからなる部材と、純
AlまたはAl合金からなる部材とを強固な接合強
度でろう付けすることができることが明らかであ
る。 上述のように、この発明の方法によれば、純
Mo、Mo合金、純W、およびW合金のうちのい
ずれかからなる重質の部材の一部を軽質の純Al
またはAl合金で置換することが可能となるので、
各種重質部材の軽量化が可能となり、さらに純
AlまたはAl合金はすぐれた冷却作用をもつので、
例えば炭酸ガスレーザー用反射鏡や真空炉の内壁
材などの製造に適用した場合、これら部材はすぐ
れた性能を長期に亘つて発揮するようになるなど
工業上有用な効果が得られるのである。
From the results shown in Table 1, in methods 1 to 8 of the present invention, pure Mo, Mo alloy, pure W, which were conventionally considered to be extremely difficult to join by brazing,
and W alloy, and pure
It is clear that a member made of Al or an Al alloy can be brazed with strong joint strength. As mentioned above, according to the method of this invention, pure
Part of a heavy member made of Mo, Mo alloy, pure W, or W alloy is replaced with light pure Al
Or it can be replaced with Al alloy, so
It is now possible to reduce the weight of various heavy components, making it even more pure.
Al or Al alloy has an excellent cooling effect, so
For example, when applied to the manufacture of reflectors for carbon dioxide lasers and inner wall materials for vacuum furnaces, these materials exhibit industrially useful effects such as superior performance over a long period of time.

Claims (1)

【特許請求の範囲】 1 純Mo、Mo合金、純W、およびW合金のう
ちのいずれかからなる被ろう付け部材のろう付け
面に、Si:3〜14重量%を含有するAl合金で構
成された平均層厚:0.1〜1mmのろう材層を固着
形成し、 ついで前記被ろう付け部材を、前記ろう材層を
介して、純AlまたはAl合金からなる基体に真空
ろう付けすることを特徴とする複合ろう付け部材
の製造法。
[Claims] 1. The brazing surface of a member to be brazed made of any one of pure Mo, Mo alloy, pure W, and W alloy is made of an Al alloy containing 3 to 14% by weight of Si. A brazing material layer having an average layer thickness of 0.1 to 1 mm is fixedly formed, and then the member to be brazed is vacuum brazed to a base made of pure Al or an Al alloy through the brazing material layer. A method for manufacturing composite brazed parts.
JP60184760A 1985-08-22 1985-08-22 Production of composite brazing member Granted JPS6245467A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP60184760A JPS6245467A (en) 1985-08-22 1985-08-22 Production of composite brazing member

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP60184760A JPS6245467A (en) 1985-08-22 1985-08-22 Production of composite brazing member

Publications (2)

Publication Number Publication Date
JPS6245467A JPS6245467A (en) 1987-02-27
JPH0338946B2 true JPH0338946B2 (en) 1991-06-12

Family

ID=16158851

Family Applications (1)

Application Number Title Priority Date Filing Date
JP60184760A Granted JPS6245467A (en) 1985-08-22 1985-08-22 Production of composite brazing member

Country Status (1)

Country Link
JP (1) JPS6245467A (en)

Families Citing this family (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
EP1392883A4 (en) * 2001-04-26 2006-04-19 Honeywell Int Inc Assemblies comprising molybdenum and aluminum; and methods of utilizing interlayers in forming target/backing plate assemblies
CN102350553B (en) * 2011-06-29 2013-06-05 哈尔滨工业大学 Welding method of high-volume-content ceramic reinforced Al-base composite material

Also Published As

Publication number Publication date
JPS6245467A (en) 1987-02-27

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