JPH0575507B2 - - Google Patents
Info
- Publication number
- JPH0575507B2 JPH0575507B2 JP61003298A JP329886A JPH0575507B2 JP H0575507 B2 JPH0575507 B2 JP H0575507B2 JP 61003298 A JP61003298 A JP 61003298A JP 329886 A JP329886 A JP 329886A JP H0575507 B2 JPH0575507 B2 JP H0575507B2
- Authority
- JP
- Japan
- Prior art keywords
- pure
- alloy
- brazing
- weight
- brazed
- 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
Links
- 238000005219 brazing Methods 0.000 claims description 22
- 239000002131 composite material Substances 0.000 claims description 8
- 229910001182 Mo alloy Inorganic materials 0.000 claims description 6
- 238000007733 ion plating Methods 0.000 claims description 6
- 239000002184 metal Substances 0.000 claims description 6
- 229910052751 metal Inorganic materials 0.000 claims description 6
- 239000000945 filler Substances 0.000 claims description 5
- 238000004519 manufacturing process Methods 0.000 claims description 5
- 229910001069 Ti alloy Inorganic materials 0.000 claims description 4
- 229910001080 W alloy Inorganic materials 0.000 claims description 4
- 229910000838 Al alloy Inorganic materials 0.000 claims description 3
- -1 pure W Inorganic materials 0.000 claims 1
- 239000010949 copper Substances 0.000 description 15
- 239000000463 material Substances 0.000 description 13
- CURLTUGMZLYLDI-UHFFFAOYSA-N Carbon dioxide Chemical compound O=C=O CURLTUGMZLYLDI-UHFFFAOYSA-N 0.000 description 12
- 238000000034 method Methods 0.000 description 7
- 229910002092 carbon dioxide Inorganic materials 0.000 description 6
- 239000001569 carbon dioxide Substances 0.000 description 6
- 229910052721 tungsten Inorganic materials 0.000 description 5
- 230000000694 effects Effects 0.000 description 4
- 230000005484 gravity Effects 0.000 description 4
- 229910052750 molybdenum Inorganic materials 0.000 description 4
- 229910045601 alloy Inorganic materials 0.000 description 3
- 239000000956 alloy Substances 0.000 description 3
- 238000012733 comparative method Methods 0.000 description 3
- 239000000203 mixture Substances 0.000 description 3
- 230000015572 biosynthetic process Effects 0.000 description 2
- 238000001816 cooling Methods 0.000 description 2
- 229910052802 copper Inorganic materials 0.000 description 2
- 239000003562 lightweight material Substances 0.000 description 2
- 238000007747 plating Methods 0.000 description 2
- 229910000679 solder Inorganic materials 0.000 description 2
- RYGMFSIKBFXOCR-UHFFFAOYSA-N Copper Chemical compound [Cu] RYGMFSIKBFXOCR-UHFFFAOYSA-N 0.000 description 1
- 238000004140 cleaning Methods 0.000 description 1
- 239000013078 crystal Substances 0.000 description 1
- 230000007423 decrease Effects 0.000 description 1
- 229910052737 gold Inorganic materials 0.000 description 1
- 150000002500 ions Chemical class 0.000 description 1
- 229910052755 nonmetal Inorganic materials 0.000 description 1
- 229910021332 silicide Inorganic materials 0.000 description 1
- FVBUAEGBCNSCDD-UHFFFAOYSA-N silicide(4-) Chemical compound [Si-4] FVBUAEGBCNSCDD-UHFFFAOYSA-N 0.000 description 1
Description
〔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
は、表面を鏡面仕上げした純Cu製のものや、さ
らにその鏡面にAuめつきを施した純Cu製のもの
などが知られている。
しかしながら、これらの純Cu製反射鏡では、
レーザー照射時間が長くなると、表面に加工材か
ら発生した金属や非金属の蒸気が付着し、その反
射率が低下するようになるばかりでなく、表面が
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ためには、定期的に
表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、鏡面やめつき面を傷つけ
易く、この結果反射特性が損なわれるようになる
ものである。
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に代つて硬質の純
Moを使用することが定着しつつある。この純
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均一な反射率を有す
る面を研摩によつて得やすく、さらに蒸発物の付
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、装置目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)純Mo製あるいは純W製の反射鏡の重量軽
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、炭酸ガスレーザーの反射鏡、さらに真空炉の
内壁材などを構成する純Mo製部材のほか、同様
に重質のMo合金、純W、あるいはW合金で構成
された各種の部材に着目し、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で構成され
た重質部材の一部を、軽量の(比重の小さい)純
TiまたはTi合金の軽量材で構成すれば、それだ
け軽量化されることになるが、例えば純Moおよ
び純Wの比重が10.2g/cm3および19.3g/cm3であ
るに対して、純Tiの比重は4.5g/cm3であり、ま
た純Moおよび純Wの熱膨張率が5.1×10-6/℃お
よび4.5×10-6/℃であるのに対して、純Tiのそ
れは8.9×10-6/℃であるように、これらの重質
材と軽量材とは種々の点で特性を異にすることに
原因し、これら両部材を高い接合強度でろう付け
することは困難であり、軽量化をはかることが不
可能であつたものを、これら両部材のろう付け面
のそれぞれに、イオンプレーテイング法により平
均層厚で0.01〜50μmのCu層を固着形成した状態
で、Si:0.5〜14重量%を含有するAl合金のろう
材を用いて真空ろう付けを行なうと、これら両部
材は強固に接合するようになり、高い接合強度で
ろう付けされた複合ろう付け部材が得られるよう
に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
のであつて、純Mo、Mo合金、純W、およびW
合金のうちのいずれかで構成された重質部材のろ
う付け面、および純TiまたはTi合金で構成され
た軽質部材のろう付け面のそれぞれに、イオンプ
レーテイング法により平均層厚で0.01〜50μmの
Cu層を固着形成し、ついで、これら両部材を、
Si:0.5〜14重量%を含有するAl合金のろう材を
用いて真空ろう付けす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、Cu層の平均
層厚を0.01〜50μmに限定したのは、その平均層
厚が0.01μm未満ではろう材とのぬれ性が不十分
で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50μmを越えると、Cu層
形成時に内部歪が残留するようになつて、ろう付
け時にCu層に剥離が発生するようになるばかり
でなく、ろう材中のCu濃度が、特に部材のろう
付け面近傍で高くなり、この結果ろう材強度が低
下するようになるという理由にもとづくものであ
る。また、同じくろう材のSi含有量については、
その含有量が0.5重量%未満では、ろう付け接合
面に形成されるけい化物層の形成が不十分で、十
分な接合強度を確保することができず、一方その
含有量が14重量%を越えると、ろう付け接合面が
脆化するようになつて、複合ろう付け部材に熱歪
が生じた場合に、接合部に剥離が発生し易くなる
ことから、その含有量を0.5〜14重量%と定めた。
さらに、上記の両部材、特に軽質部材の表面に
は、ろう材のぬれ性を低下させる酸化皮膜が存在
するが、イオンプレーテイング法によれば、この
酸化皮膜を除去しながら、Cu層を形成すること
が可能となり、この結果ろう材のぬれ性が著しく
向上するようになることから、イオンプレーテイ
ング法によるCu層形成は不可欠であり、特にろ
う付けが面接合になる場合には一段とその必要性
を増すものである。
〔実施例〕
つぎに、この発明の方法を実施例により具体的
に説明する。
重質部材として、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
をもつた各種部材を用意し、また軽質部材とし
て、同じく第1表に示される組成を有し、かつ直
径:100mm×厚さ:18mmの寸法をもつた各種部材
を用意し、ついで、これら部材のろう付け面とな
る片側面に、イオンプレーテイング装置を用い、
通常の条件にて、イオンクリーニングした後、同
じく第1表に示される平均層厚のCu層を固着形
成し、引続いて、同じく第1表に示される組成を
有する厚さ:0.3mmのろう材を、両部材のろう付
け面間にはさんだ状態で、重質部材を下側にして
重ね合わせ、この上に20Kgの重りを置き、通常の
条件、すなわち圧力:1×10-4torrの真空中、温
度:620℃に15分間保持の条件で真空ろう付けを
行なうことによつて、本発明法1〜4および比較
法1〜4をそれぞれ実施した。
なお、比較法1〜4は、いずれかの条件(第1
[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, as reflectors for carbon dioxide gas, for example, mirrors made of pure Cu with a mirror finish, and mirrors made of pure Cu with an Au plating on the mirror surface have been known. There is. However, with these pure Cu reflectors,
As the laser irradiation time increases, metal and non-metal vapor generated from the processed material adheres to the surface, which not only reduces its reflectance, but also causes the surface to absorb the laser energy, melt, and reflect. Accidents such as damaging mirrors have occurred. In order to prevent such accidents, it is necessary to regularly remove deposits from the surface, but since the pure Cu and Au plating that makes up the reflector is very soft, when wiping it off, it is necessary to remove the deposits from the surface. The surface is easily damaged, resulting in loss of reflective properties. For this reason, in recent years, hard pure copper has been used as a material for carbon dioxide laser reflectors, replacing pure Cu.
The use of Mo is becoming established. This purity
Mo reflecting mirrors, especially single crystal ones and polycrystal ones with fine grains, are easy to polish to provide a surface with uniform reflectance, and also have excellent performance with less adhesion of evaporated matter. It is something that demonstrates the. [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 need for lighter weight devices. Accordingly, there is a strong desire to reduce the weight of reflective mirrors made of pure Mo or pure W, which have a high specific gravity (heavy). [Means for Solving the Problems] Therefore, from the above-mentioned viewpoint, the present inventors have developed a material made of pure Mo that constitutes the reflecting mirror of the carbon dioxide laser, the inner wall material of the vacuum furnace, and the like. As a result of focusing on various parts made of heavy Mo alloy, pure W, or W alloy, and conducting research to reduce their weight, we found that pure Mo, Mo alloy,
A part of a heavy member made of either pure W or W alloy is replaced with lightweight (low specific gravity) pure W.
If it is made of lightweight material such as Ti or Ti alloy, the weight will be reduced accordingly, but for example, the specific gravity of pure Mo and pure W is 10.2 g/cm 3 and 19.3 g/cm 3 , while pure Ti The specific gravity of is 4.5 g/ cm3 , and the coefficient of thermal expansion of pure Mo and pure W is 5.1×10 -6 /℃ and 4.5×10 -6 /℃, while that of pure Ti is 8.9× 10 -6 /℃, these heavy materials and lightweight materials have different characteristics in various respects, and it is difficult to braze these two materials with high joint strength. However, it was impossible to reduce the weight of these parts by forming a Cu layer with an average thickness of 0.01 to 50 μm on each of the brazed surfaces of these two parts using the ion plating method. When vacuum brazing is performed using an Al alloy brazing filler metal containing 0.5 to 14% by weight, these two components will be firmly joined, resulting in a composite brazed component that is brazed with high joint strength. I have gained knowledge that this will happen. This invention was made based on the above knowledge, and it is based on pure Mo, Mo alloy, pure W, and W.
An average layer thickness of 0.01 to 50 μm is applied by ion plating to the brazing surface of a heavy component made of any of the alloys and the brazing surface of a light component made of pure Ti or a Ti alloy. of
The Cu layer is fixedly formed, and then these two members are bonded together.
This method is characterized by a method of manufacturing a composite brazing member in which vacuum brazing is performed using an Al alloy brazing filler metal containing 0.5 to 14% by weight of Si. In the method of this invention, the average layer thickness of the Cu layer is limited to 0.01 to 50 μm because if the average layer thickness is less than 0.01 μm, the wettability with the brazing material will be insufficient and the desired strong bonding strength will not be achieved. On the other hand, if the average layer thickness exceeds 50 μm, internal strain will remain during the formation of the Cu layer, which will not only cause peeling of the Cu layer during brazing, but also cause the solder to deteriorate. This is based on the fact that the Cu concentration in the material becomes high, especially near the brazing surface of the component, and as a result, the strength of the brazing material decreases. Also, regarding the Si content of the filler metal,
If the content is less than 0.5% by weight, the formation of a silicide layer on the brazed joint surface will be insufficient, making it impossible to ensure sufficient joint strength, while if the content exceeds 14% by weight If the brazed joint surface becomes brittle and thermal distortion occurs in the composite brazed component, peeling will easily occur at the joint, so the content should be set at 0.5 to 14% by weight. Established.
Furthermore, on the surfaces of both of the above-mentioned components, especially the light components, there is an oxide film that reduces the wettability of the brazing filler metal, but according to the ion plating method, this oxide film is removed while forming a Cu layer. This makes it possible to significantly improve the wettability of the brazing material, so forming a Cu layer using the ion plating method is essential, and it is especially necessary when brazing involves face-to-face bonding. It increases sex. [Example] Next, the method of the present invention will be specifically explained with reference to Examples. As heavy members, various members having the composition shown in Table 1 and having dimensions of diameter: 100 mm x thickness: 2 mm were prepared, and as light members, the compositions also shown in Table 1 were prepared. Prepare various parts with dimensions of 100 mm in diameter x 18 mm in thickness, then use an ion plating device on one side of these parts to be brazed.
After ion cleaning under normal conditions, a Cu layer of the average layer thickness also shown in Table 1 is fixedly formed, followed by a solder with a thickness of 0.3 mm having the composition also shown in Table 1. The materials are sandwiched between the brazed surfaces of both components, with the heavy component facing down, and a 20 kg weight is placed on top of this, under normal conditions, that is, a pressure of 1 x 10 -4 torr. Methods 1 to 4 of the present invention and comparative methods 1 to 4 were carried out by performing vacuum brazing under conditions of holding the temperature at 620° C. for 15 minutes in a vacuum. In addition, Comparative Methods 1 to 4 are based on any of the conditions (first
第1表に示される結果から、本発明法1〜4に
より製造された複合ろう付け部材においては、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、および合金
のうちのいずれかからなる重質部材、純Tiまた
はTi合金からなる軽質部材とが強固な接合強度
でろう付けされていることが明らかである。
これに対して、比較法1〜4に見られるよう
に、条件のうちのいずれかの条件でもこの発明の
範囲から外れると強固な接合強度でろう付けする
ことがないのである。
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
ずれかで構成された重質部材と、純TiまたはTi
合金で構成された軽質部材とを強固な接合強度で
ろう付けすることができるので、前記重質部材の
一部を前記軽質部材で置換することが可能とな
り、それだけ軽量化した複合ろう付け部材を製造
することができるようになるほか、前記軽質部材
は、高強度およびすぐれた冷却効果をもつので、
例えば炭酸ガスレーザー用反射鏡や真空炉の内壁
材などの製造に用いた場合には、この結果得られ
た複合ろう付は部材が熱サイクルに対してすぐれ
た耐久性をもつことと合まつて、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
な効果がもたらされるのである。
From the results shown in Table 1, it can be seen that in the composite brazed parts manufactured by methods 1 to 4 of the present invention, pure Mo, Mo alloy, pure W, which were conventionally considered to be extremely difficult to join by brazing, It is clear that the heavy member made of any of these alloys and the light member made of pure Ti or Ti alloy are brazed with strong joint strength. On the other hand, as seen in Comparative Methods 1 to 4, if any of the conditions falls outside the scope of the present invention, brazing with strong bonding strength will not be achieved. As mentioned above, according to the method of this invention, pure
A heavy member made of Mo, Mo alloy, pure W, or W alloy, and pure Ti or Ti
Since it is possible to braze a light member made of an alloy with a strong joint strength, it is possible to replace a part of the heavy member with the light member, making it possible to create a composite brazed member that is lighter in weight. In addition to being easy to manufacture, the lightweight member has high strength and excellent cooling effect.
For example, when used in the manufacture of reflectors for carbon dioxide lasers or inner wall materials for vacuum furnaces, the resulting composite brazing is combined with the excellent durability of the components against thermal cycles. This brings about industrially useful effects such as superior performance over a long period of time.
Claims (1)
ちのいずれかで構成された重質部材のろう付け
面、並びに純TiまたはTi合金で構成された軽質
部材のろう付け面のそれぞれに、イオンプレーテ
イング法により、平均層厚で0.01〜50μmのCu層
を固着形成し、 ついで、これら両部材を、Si:0.5〜14重量%
を含有するAl合金からなるろう材を用いて真空
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. A brazing surface of a heavy member made of pure Mo, a Mo alloy, pure W, or a W alloy, and a brazing surface of a light member made of pure Ti or a Ti alloy. A Cu layer with an average layer thickness of 0.01 to 50 μm is fixedly formed on each of the mounting surfaces by ion plating method, and then both these members are coated with Si: 0.5 to 14% by weight.
1. A method for producing a composite brazed member, which comprises performing vacuum brazing using a brazing filler metal made of an Al alloy containing
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP61003298A JPS62161467A (en) | 1986-01-10 | 1986-01-10 | Production of composite brazing member |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP61003298A JPS62161467A (en) | 1986-01-10 | 1986-01-10 | Production of composite brazing member |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| JPS62161467A JPS62161467A (en) | 1987-07-17 |
| JPH0575507B2 true JPH0575507B2 (en) | 1993-10-20 |
Family
ID=11553465
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP61003298A Granted JPS62161467A (en) | 1986-01-10 | 1986-01-10 | Production of composite brazing member |
Country Status (1)
| Country | Link |
|---|---|
| JP (1) | JPS62161467A (en) |
-
1986
- 1986-01-10 JP JP61003298A patent/JPS62161467A/en active Granted
Also Published As
| Publication number | Publication date |
|---|---|
| JPS62161467A (en) | 1987-07-17 |
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