JP2717918B2 - Metal composite parts - Google Patents
Metal composite partsInfo
- Publication number
- JP2717918B2 JP2717918B2 JP5164516A JP16451693A JP2717918B2 JP 2717918 B2 JP2717918 B2 JP 2717918B2 JP 5164516 A JP5164516 A JP 5164516A JP 16451693 A JP16451693 A JP 16451693A JP 2717918 B2 JP2717918 B2 JP 2717918B2
- Authority
- JP
- Japan
- Prior art keywords
- base material
- metal composite
- thermal expansion
- substrate
- expansion coefficient
- 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
- 239000002905 metal composite material Substances 0.000 title claims description 21
- 239000000463 material Substances 0.000 claims description 57
- 239000002131 composite material Substances 0.000 claims description 33
- 239000000758 substrate Substances 0.000 claims description 24
- 239000010949 copper Substances 0.000 claims description 18
- 238000000034 method Methods 0.000 claims description 12
- 238000007747 plating Methods 0.000 claims description 12
- 238000005219 brazing Methods 0.000 claims description 8
- XAGFODPZIPBFFR-UHFFFAOYSA-N aluminium Chemical compound [Al] XAGFODPZIPBFFR-UHFFFAOYSA-N 0.000 claims description 7
- 229910001026 inconel Inorganic materials 0.000 claims description 6
- 239000010935 stainless steel Substances 0.000 claims description 6
- 229910001220 stainless steel Inorganic materials 0.000 claims description 6
- 229910001374 Invar Inorganic materials 0.000 claims description 5
- ZOKXTWBITQBERF-UHFFFAOYSA-N Molybdenum Chemical compound [Mo] ZOKXTWBITQBERF-UHFFFAOYSA-N 0.000 claims description 5
- RTAQQCXQSZGOHL-UHFFFAOYSA-N Titanium Chemical compound [Ti] RTAQQCXQSZGOHL-UHFFFAOYSA-N 0.000 claims description 5
- 238000004880 explosion Methods 0.000 claims description 5
- 229910052750 molybdenum Inorganic materials 0.000 claims description 5
- 239000011733 molybdenum Substances 0.000 claims description 5
- 239000010936 titanium Substances 0.000 claims description 5
- 229910052719 titanium Inorganic materials 0.000 claims description 5
- 229910000838 Al alloy Inorganic materials 0.000 claims description 4
- 229910000676 Si alloy Inorganic materials 0.000 claims description 4
- 229910052782 aluminium Inorganic materials 0.000 claims description 4
- RYGMFSIKBFXOCR-UHFFFAOYSA-N Copper Chemical compound [Cu] RYGMFSIKBFXOCR-UHFFFAOYSA-N 0.000 claims description 3
- 229910052802 copper Inorganic materials 0.000 claims description 3
- 229910000831 Steel Inorganic materials 0.000 claims 2
- 239000010959 steel Substances 0.000 claims 2
- 239000010410 layer Substances 0.000 description 28
- 239000004065 semiconductor Substances 0.000 description 23
- PXHVJJICTQNCMI-UHFFFAOYSA-N Nickel Chemical compound [Ni] PXHVJJICTQNCMI-UHFFFAOYSA-N 0.000 description 12
- 238000005096 rolling process Methods 0.000 description 9
- 230000017525 heat dissipation Effects 0.000 description 8
- 239000013585 weight reducing agent Substances 0.000 description 7
- 238000005304 joining Methods 0.000 description 5
- 230000005855 radiation Effects 0.000 description 5
- HCHKCACWOHOZIP-UHFFFAOYSA-N Zinc Chemical compound [Zn] HCHKCACWOHOZIP-UHFFFAOYSA-N 0.000 description 3
- 238000004519 manufacturing process Methods 0.000 description 3
- 230000003647 oxidation Effects 0.000 description 3
- 238000007254 oxidation reaction Methods 0.000 description 3
- 229910000679 solder Inorganic materials 0.000 description 3
- 230000003746 surface roughness Effects 0.000 description 3
- 229910052725 zinc Inorganic materials 0.000 description 3
- 239000011701 zinc Substances 0.000 description 3
- 229910021364 Al-Si alloy Inorganic materials 0.000 description 2
- 239000000919 ceramic Substances 0.000 description 2
- 238000005097 cold rolling Methods 0.000 description 2
- 238000005260 corrosion Methods 0.000 description 2
- 230000007797 corrosion Effects 0.000 description 2
- 238000010438 heat treatment Methods 0.000 description 2
- 239000000126 substance Substances 0.000 description 2
- 238000006467 substitution reaction Methods 0.000 description 2
- 239000002344 surface layer Substances 0.000 description 2
- 229910018072 Al 2 O 3 Inorganic materials 0.000 description 1
- 208000019901 Anxiety disease Diseases 0.000 description 1
- JBRZTFJDHDCESZ-UHFFFAOYSA-N AsGa Chemical compound [As]#[Ga] JBRZTFJDHDCESZ-UHFFFAOYSA-N 0.000 description 1
- 229910000881 Cu alloy Inorganic materials 0.000 description 1
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 description 1
- XUIMIQQOPSSXEZ-UHFFFAOYSA-N Silicon Chemical compound [Si] XUIMIQQOPSSXEZ-UHFFFAOYSA-N 0.000 description 1
- 229910020816 Sn Pb Inorganic materials 0.000 description 1
- 229910020922 Sn-Pb Inorganic materials 0.000 description 1
- 229910008783 Sn—Pb Inorganic materials 0.000 description 1
- PNEYBMLMFCGWSK-UHFFFAOYSA-N aluminium oxide Inorganic materials [O-2].[O-2].[O-2].[Al+3].[Al+3] PNEYBMLMFCGWSK-UHFFFAOYSA-N 0.000 description 1
- 230000036506 anxiety Effects 0.000 description 1
- 238000013459 approach Methods 0.000 description 1
- 238000005253 cladding Methods 0.000 description 1
- 238000002788 crimping Methods 0.000 description 1
- 230000002950 deficient Effects 0.000 description 1
- 238000013461 design Methods 0.000 description 1
- 238000011549 displacement method Methods 0.000 description 1
- 230000000694 effects Effects 0.000 description 1
- 238000002474 experimental method Methods 0.000 description 1
- 239000002360 explosive Substances 0.000 description 1
- -1 for example Substances 0.000 description 1
- 230000020169 heat generation Effects 0.000 description 1
- 238000005098 hot rolling Methods 0.000 description 1
- 229910052739 hydrogen Inorganic materials 0.000 description 1
- 239000001257 hydrogen Substances 0.000 description 1
- 238000003475 lamination Methods 0.000 description 1
- 230000013011 mating Effects 0.000 description 1
- 239000007769 metal material Substances 0.000 description 1
- 229910052759 nickel Inorganic materials 0.000 description 1
- 230000002093 peripheral effect Effects 0.000 description 1
- 238000012545 processing Methods 0.000 description 1
- 230000000191 radiation effect Effects 0.000 description 1
- 229910052710 silicon Inorganic materials 0.000 description 1
- 239000010703 silicon Substances 0.000 description 1
- 229910052718 tin Inorganic materials 0.000 description 1
- 229910052721 tungsten Inorganic materials 0.000 description 1
Landscapes
- Pressure Welding/Diffusion-Bonding (AREA)
- Laminated Bodies (AREA)
- Structures Or Materials For Encapsulating Or Coating Semiconductor Devices Or Solid State Devices (AREA)
- Insulated Metal Substrates For Printed Circuits (AREA)
- Cooling Or The Like Of Semiconductors Or Solid State Devices (AREA)
Description
【0001】[0001]
【産業上の利用分野】本発明は、半導体集積回路装置に
用いる金属複合部品に関し、特に、パッケージ内に半導
体素子を搭載すると共に半導体素子の発する熱を放熱す
る基板(以後、放熱基板と呼ぶ)として用いるのに適し
た金属複合部品に関する。BACKGROUND OF THE INVENTION 1. Field of the Invention The present invention relates to a metal composite component used in a semiconductor integrated circuit device, and more particularly to a substrate for mounting a semiconductor element in a package and radiating heat generated by the semiconductor element (hereinafter referred to as a heat radiation substrate). Metal composite parts suitable for use as
【0002】[0002]
【従来の技術】従来、半導体集積回路装置に使用される
放熱基板として、半導体素子の固着工程における加熱作
業や、集積回路の高密度化および高出力化に伴う発熱量
の増加に対処できるように、高い放熱効果を有するもの
が要求されている。また、高い放熱効果に加えて、放熱
基板には、半導体素子の材料、例えば、シリコン(S
i)やガリウム砒素(GaAs)等に対する熱膨張率の
マッチングがとれていることも要求されている。2. Description of the Related Art Conventionally, as a heat-radiating substrate used in a semiconductor integrated circuit device, it has been required to cope with a heating operation in a fixing step of a semiconductor element and an increase in heat generation due to an increase in density and output of an integrated circuit. What has a high heat dissipation effect is demanded. In addition to the high heat radiation effect, the heat radiation substrate is provided with a semiconductor element material, for example, silicon (S
It is also required that the thermal expansion coefficient of i) and gallium arsenide (GaAs) be matched.
【0003】一般に、大電力用半導体装置に使用される
放熱基板として、特開平2−102551号公報に記載
されたものがある。ここでは、放熱基板の熱膨張係数
を、半導体集積回路を構成するSi等の半導体材料や、
半導体搭載用セラミックス(Al2 O3 等)基板の熱膨
張係数に近くするために、モリブデン(Mo)を基材と
し、この基材の両側に銅(Cu)またはCu合金を被覆
した複合材料が提案されている。[0003] Generally, as a heat dissipation board used in a high power semiconductor device, there is one described in Japanese Patent Application Laid-Open No. 2-102551. Here, the thermal expansion coefficient of the heat dissipation substrate is determined by using a semiconductor material such as Si forming a semiconductor integrated circuit,
In order to approach the thermal expansion coefficient of a ceramic substrate for mounting semiconductors (such as Al 2 O 3 ), a composite material in which molybdenum (Mo) is used as a base material and both sides of the base material are coated with copper (Cu) or a Cu alloy is used. Proposed.
【0004】一方、最近、半導体集積回路装置の軽量化
に対する要求が強くなってきている。このように、軽量
化を重視した半導体集積回路装置においては、半導体集
積回路を支持する基板だけでなく、放熱基板を軽くする
ことが強く要求され、半導体材料に比較して、大きな熱
膨張係数を有する放熱基板も許容される傾向にある。On the other hand, recently, there has been an increasing demand for weight reduction of semiconductor integrated circuit devices. As described above, in a semiconductor integrated circuit device which emphasizes weight reduction, not only a substrate supporting the semiconductor integrated circuit but also a heat dissipation substrate is strongly required to be light, and a large thermal expansion coefficient is required as compared with a semiconductor material. There is also a tendency for the heat radiation substrate to be allowed.
【0005】[0005]
【発明が解決しようとする課題】このような要求に応え
るためには、放熱基板を比較的密度の低い材料、即ち、
軽い材料で構成することが必要であるが、密度の低い材
料、例えば、アルミニウム(Al)は、一般にSi等の
半導体材料に比較して、熱膨張係数が余りにも高いた
め、熱膨張係数の点で許容される範囲にはない。In order to meet such a demand, a heat-radiating substrate is made of a material having a relatively low density, that is, a material having a relatively low density.
Although it is necessary to be made of a light material, a low-density material, for example, aluminum (Al) generally has a thermal expansion coefficient that is too high as compared with a semiconductor material such as Si. Is not within the allowable range.
【0006】尚、上記した大電力用半導体装置に使用さ
れる放熱基板を、軽量化を要求される半導体集積回路装
置に適用したとしても、軽量化、熱膨張係数、密着強度
の点で問題があった。[0006] Even if the heat-dissipating substrate used in the high-power semiconductor device described above is applied to a semiconductor integrated circuit device that requires a reduction in weight, there are problems in terms of weight reduction, thermal expansion coefficient, and adhesion strength. there were.
【0007】そして、本発明者等の実験によれば、軽量
化の要求に応えるために、23.0×10-6/K以上の
熱膨張係数を有するAlは熱膨張係数および熱伝導率の
面で不適当であるが、熱膨張係数が10×10-6/K程
度であれば、十分使用に耐え得る放熱基板が得られてい
る。According to experiments by the present inventors, Al having a thermal expansion coefficient of 23.0 × 10 −6 / K or more is required to meet the demand for weight reduction. Although it is unsuitable in terms of surface, if the coefficient of thermal expansion is about 10.times.10.sup.-6 / K, a heat dissipation board that can withstand sufficient use is obtained.
【0008】本発明の課題は、軽量化の要求に応え得る
と共に、熱膨張係数、熱伝導率の点でも十分な金属複合
部品およびその製造方法を提供することである。An object of the present invention is to provide a metal composite component which can meet the demand for weight reduction and has a sufficient thermal expansion coefficient and thermal conductivity, and a method for producing the same.
【0009】[0009]
【課題を解決するための手段】本発明によれば、少くと
も一層の基材と、該基材に接合された少くとも一層の合
せ材とにより構成される金属複合部品において、前記基
材は、モリブデンおよびアルミニウム/シリコン合金の
うちのどちらか一方であり、前記合せ材は、前記基材が
モリブデンの場合には、ステンレス、インバー、インコ
ネル、およびチタンのうちから選ばれた少くとも1種で
あり、前記基材がアルミニウム/シリコン合金の場合に
は、銅、アルミニウム、ステンレス、インバー、インコ
ネル、およびチタンのうちから選ばれた少くとも1種で
あり、前記基材および前記合せ材は、爆発圧着工程また
はろう付け工程を含む工程により接合されており、複合
部品全体の熱膨脹係数が10.0×10-6/Kよりも大
きく23.0×10-6/Kよりも小さい範囲にあり、か
つ、(前記合せ材の層厚/前記基材の層厚)で定義され
る層厚比が3/1乃至9/1であることを特徴とする金
属複合部品が得られる。According to the present invention, there is provided a metal composite component comprising at least one base material and at least one bonding material joined to the base material, wherein the base material is , Molybdenum or an aluminum / silicon alloy, and the bonding material is at least one selected from stainless steel, invar, inconel, and titanium when the base material is molybdenum. If the substrate is an aluminum / silicon alloy, it is at least one selected from copper, aluminum, stainless steel, invar, inconel, and titanium, and the substrate and the composite crimping process or brazing process are joined by a process comprising the thermal expansion coefficient of the entire composite part is 10.0 × 10 -6 / greater than K 23.0 × 1 There range smaller than -6 / K, and wherein the layer thickness ratio defined by (thickness of layer thickness / the base material of the cladding material) is 3/1 to 9/1 A metal composite part is obtained.
【0010】本発明によればまた、前記熱膨脹係数が1
3.0×10-6/K乃至15.0×10-6/Kであるこ
とを特徴とする前記金属複合部品が得られる。According to the present invention, the thermal expansion coefficient is 1
The metal composite component having a ratio of 3.0 × 10 −6 / K to 15.0 × 10 −6 / K is obtained.
【0011】本発明によればさらに、前記合せ材の表面
に、めっき層を有することを特徴とする前記金属複合部
品が得られる。本発明によればまた、前記基材と前記合
せ材との接する境界面に、めっき層を有することを特徴
とする前記金属複合部品が得られる。According to the present invention, there is further provided the metal composite component having a plating layer on a surface of the composite material. According to the present invention, the metal composite component having a plating layer on a boundary surface between the base material and the composite material is obtained.
【0012】尚、前記基材として、前記熱膨張係数の範
囲内で低め狙いのものにはMoを用い、高め狙いのもの
にはAl合金を用いることで、熱特性の所望の範囲での
自由度を増している。It is to be noted that Mo is used for the base material having a lower thermal expansion coefficient and Al alloy is used for the base material having a higher thermal expansion coefficient. Increasing degrees.
【0013】また、前記合せ材については、軽量で熱伝
導性の良好な金属材料から選択されるが、この条件以外
に、めっき層を施すことによりろう付性の向上や耐蝕性
の向上を期待できるか、合せ材自体で耐酸化性や耐薬品
性の向上が期待できるものに限定した。前者はCu、A
lであり、後者はステンレス、インバー、インコネル、
チタンである。In addition, the above-mentioned composite material is selected from a metal material which is lightweight and has good thermal conductivity. Except for these conditions, it is expected to improve brazing properties and corrosion resistance by applying a plating layer. It is limited to those that can be expected to improve the oxidation resistance and chemical resistance of the composite material itself. The former is Cu, A
l, the latter being stainless steel, invar, inconel,
It is titanium.
【0014】また、上記したように、爆発圧着工程後に
圧延工程を行うことにより、層比および外表面を整え
て、接合強度の向上と表面の平滑性の向上を図ってい
る。Further, as described above, by performing the rolling step after the explosion pressure bonding step, the layer ratio and the outer surface are adjusted to improve the bonding strength and the surface smoothness.
【0015】さらに、前述したように、ろう付け工程と
圧延工程とを行った場合は、ろう付け工程によって設計
した層厚比通りの基材と合せ材を100〜400℃で接
合し、その後圧延によって外表面を整えることなる。こ
れにより、めっきがし易くなるか、あるいは、半導体集
積回路との接合がし易くなる。この方法によれば、いず
れも層厚比を大幅に、例えば、Cu/Mo=1/1〜2
/1をCu/Mo=3/1〜9/1程度に上げることが
できる。しかも、圧延を施した場合、高品質安定な金属
複合部品(クラッド材)にし得る。Further, as described above, when the brazing step and the rolling step are performed, the base material and the composite material having the layer thickness ratio designed by the brazing step are joined at 100 to 400 ° C., and then the rolling is performed. The outer surface is thereby adjusted. This facilitates plating or joining with a semiconductor integrated circuit. According to this method, the layer thickness ratio is greatly increased, for example, Cu / Mo = 1/1 to 2
/ 1 can be increased to about Cu / Mo = 3/1 to 9/1. Moreover, when rolling is performed, a high-quality and stable metal composite component (clad material) can be obtained.
【0016】また、層厚比が大きくなれば、仮に加熱し
ても接合での安定性には不安が残る場合が考えられる。
この場合には、ろう付け工程では、基材と合せ材との間
に接合適正温度を低下すると共に、密着性を保持および
向上させるために、濡れ性のよい薄層(めっき層)を接
合補助層として介する。Further, if the layer thickness ratio becomes large, there may be a case where even if the layer is heated, the stability at the time of bonding remains uneasy.
In this case, in the brazing step, a proper bonding temperature between the base material and the composite material is lowered, and a thin layer (plating layer) having good wettability is assisted in order to maintain and improve the adhesion. Intermediate as a layer.
【0017】[0017]
【実施例】以下、本発明の実施例による金属複合部品
を、その製造工程にそくして説明する。DESCRIPTION OF THE PREFERRED EMBODIMENTS A metal composite part according to an embodiment of the present invention will be described below along with its manufacturing process.
【0018】[実施例1]基材用素材として厚さ0.2
mmのMo板を用意し、合せ材用素材に厚さ1.5mm
のCu板を用意した。基材の両面に合せ材を配し、即
ち、Cu/Mo/Cuの3層形態になる様に位置させ、
爆発圧着法により接合させた。Example 1 A substrate material having a thickness of 0.2
Prepare a 1.5mm thick Mo plate and add 1.5mm
Was prepared. Placing a mating material on both sides of the base material, that is, positioning it in a three-layer form of Cu / Mo / Cu,
They were joined by an explosion pressure bonding method.
【0019】次いで、この接合体を圧延により、厚さ
2.0mmにまで加工し、Cu/Mo/Cuの3層が、
層厚比で7:1:7となる複合材に調整した。最終圧延
工程では、特に冷間圧延を施して、表面粗さをRmax.2
μmとした。このように接合された複合材を800℃で
30分熱処理して、歪みを除去する。Next, the joined body was processed to a thickness of 2.0 mm by rolling, and three layers of Cu / Mo / Cu were formed.
The composite material was adjusted to have a layer thickness ratio of 7: 1: 7. In the final rolling step, particularly, cold rolling is performed to reduce the surface roughness to Rmax.2.
μm. The composite material thus joined is heat-treated at 800 ° C. for 30 minutes to remove the distortion.
【0020】この複合材は、Cu94wt%−Moの所
謂複合クラッド材となっている。その熱特性を実測した
ところ、熱膨張係数15.3×10-6/K、熱伝導率
0.80cal/cm・sec・℃であった。しかも、
密度は8.95g/cm3 であった。This composite material is a so-called composite clad material of 94 wt% Cu-Mo. When the thermal characteristics were actually measured, the thermal expansion coefficient was 15.3 × 10 −6 / K and the thermal conductivity was 0.80 cal / cm · sec · ° C. Moreover,
The density was 8.95 g / cm 3 .
【0021】尚、半導体集積回路を放熱基板に搭載する
に際し、半導体素子が接合される搭載面を可及的半導体
素子の熱膨張率に近い値(熱膨張率が比較的低い値)に
設定する一方で、この搭載面の反対側である放熱側の面
を熱伝導を優先したものとしたい場合があるが、この場
合には、搭載面をMoに、放熱面をCuとした、Mo/
Cuの2層接合の組合せが適している。この構成も爆発
圧着により容易に作製する事ができる。この2層接合の
接合材は、圧延を施して仕上げることにより、表面粗さ
をRmax.5μm以下の良好な結果が得られた。When the semiconductor integrated circuit is mounted on the heat dissipation substrate, the mounting surface to which the semiconductor element is bonded is set to a value as close as possible to the coefficient of thermal expansion of the semiconductor element (a value having a relatively low coefficient of thermal expansion). On the other hand, there is a case where it is desired to give priority to heat conduction on the heat radiation side opposite to the mounting surface. In this case, the mounting surface is made Mo and the heat radiation surface is made Cu.
A combination of two layers of Cu is suitable. This configuration can also be easily manufactured by explosive pressure bonding. The joining material of this two-layer joining was rolled and finished to obtain good results with a surface roughness of Rmax.5 μm or less.
【0022】[実施例2]基材用素材に厚さ1.0mm
のMo板を用意し、合せ材用素材として厚さ3.50m
mのCu板を用意した。そして、Mo/Cu/Moの3
層形態になる様に位置させ、爆発圧着法により接合させ
た。Example 2 A substrate material having a thickness of 1.0 mm
Prepare Mo plate of thickness 3.50m as material for composite material
m Cu plate was prepared. And 3 of Mo / Cu / Mo
They were positioned so as to form a layer and were joined by an explosion pressure bonding method.
【0023】次いで、この接合体を圧延により、厚さ
5.3mmにまで加工し、Mo/Cu/Moの3層が、
層厚比で1:3.3:1となる複合材に調整した。最終
圧延工程では、冷間圧延を施し、表面粗さをRmax.2.
5μmとした。このように接合された複合材を850℃
で25分熱処理して、歪みを除去する。Next, the joined body was processed to a thickness of 5.3 mm by rolling, and three layers of Mo / Cu / Mo were formed.
The composite material was adjusted to have a layer thickness ratio of 1: 3.3: 1. In the final rolling step, cold rolling is performed to reduce the surface roughness to Rmax.
The thickness was 5 μm. The composite material thus joined is heated to 850 ° C.
For 25 minutes to remove distortion.
【0024】この複合材は、Cu59.1wt%−Mo
の所謂複合クラッド材となっている。その熱特性を実測
したところ、熱膨張係数10.27×10-6/K、熱伝
導率0.70cal/cm・sec・℃であった。しか
も、密度は9.41g/cm3 であった。This composite material has a Cu content of 59.1 wt% -Mo.
Is a so-called composite clad material. When the thermal characteristics were measured, the thermal expansion coefficient was 10.27 × 10 −6 / K and the thermal conductivity was 0.70 cal / cm · sec · ° C. Moreover, the density was 9.41 g / cm 3 .
【0025】尚、実施例2では、基本的に前述の実施例
1と同様の熱的特性を狙ったが、この他に、外表面に比
較的剛性の高いMoが配されているため、組み立て時の
きず形成の不安を減ずると共に、Moが半導体素子に近
い熱膨張係数を有するため、複合クラッド材における各
層の積層方向に平行な方向での膨脹差に起因する剥離不
安の減少も期待できる。また、はんだなどのろう材やメ
ッキ層が比較的形成し易く、これらの工程への対応性に
優れたものである。In the second embodiment, basically, the same thermal characteristics as those in the first embodiment are aimed. However, since Mo having a relatively high rigidity is arranged on the outer surface, the assembling is performed. Since Mo has a thermal expansion coefficient close to that of a semiconductor element, it is expected that Mo has a thermal expansion coefficient close to that of a semiconductor element, and thus, it is possible to reduce anxiety of peeling due to a difference in expansion in a direction parallel to a lamination direction of each layer in the composite clad material. In addition, a brazing material such as solder and a plating layer are relatively easily formed, and are excellent in compatibility with these steps.
【0026】[実施例3]基材用素材として厚さ0.1
mmのMo板を用意し、合せ材用素材として厚さ3mm
のAl板を用意した。合せ材のAlの外表面は酸洗浄さ
れ、次に外表面上に、一般的な亜鉛置換法により厚さ5
μmにニッケル(Ni)めっきが施される。一方、基材
のMoの表面には、電解Niめっきが施され、厚さ3μ
mにNi層が形成された。Example 3 The thickness of the substrate material was 0.1
mm Mo plate is prepared and 3mm thick
Was prepared. The outer surface of Al of the composite material is acid-cleaned, and then the outer surface is coated with a thickness of 5 mm by a general zinc displacement method.
The μm is plated with nickel (Ni). On the other hand, the surface of Mo of the base material is subjected to electrolytic Ni plating to have a thickness of 3 μm.
A Ni layer was formed on m.
【0027】次に、40%Sn−Pbはんだにより、3
00℃でろう付(接合)し、所望のAl/Mo/Alの
クラッド複合材が得られた。Next, 3% by 40% Sn-Pb solder
Brazing (joining) was performed at 00 ° C. to obtain a desired clad composite material of Al / Mo / Al.
【0028】この複合材の熱特性を測った所、熱膨張係
数22.4×10-6/KとAl単独よりも低い熱膨張係
数を有し、熱伝導率0.55cal/cm・sec・℃
とAl単独より優れた熱伝導率を備えていた。尚、この
複合材の密度は2.8g/cm3 であった。即ち、実施
例3による金属複合部品は、極めて軽量かつ高い熱膨張
係数を有すると共に、熱伝導率においてもAlより優れ
ていることがわかる。When the thermal properties of this composite material were measured, it had a thermal expansion coefficient of 22.4 × 10 −6 / K, which was lower than that of Al alone, and a thermal conductivity of 0.55 cal / cm · sec · ° C
And Al had better thermal conductivity than Al alone. Incidentally, the density of this composite material was 2.8 g / cm 3 . That is, it is understood that the metal composite part according to Example 3 has an extremely lightweight and high coefficient of thermal expansion, and is also superior in thermal conductivity to Al.
【0029】しかも、この材料は、このまま冷間圧延し
て総厚を小さくする場合にはAlが優先加工されるた
め、Al/Mo比率をめっき層に割れの入らぬ範囲で容
易に変更できる。即ち、取扱いの厄介な薄い材料の状態
ではなく、比較的厚さを有する状態で接合すればよく、
製造工程の煩わしさや不良品率を抑えることができる。In addition, when this material is cold-rolled as it is to reduce the total thickness, Al is preferentially worked, so that the Al / Mo ratio can be easily changed within a range where the plating layer does not crack. That is, it is sufficient to join in a relatively thick state, not in a thin material state that is troublesome to handle,
The trouble of the manufacturing process and the defective product rate can be suppressed.
【0030】また、合せ材によりMoへCuめっきした
い場合、Niストライク処理した後に電解Cuめっきす
れば良い。In the case where Cu is to be plated on Mo using a combination material, electrolytic Cu plating may be performed after Ni strike processing.
【0031】[実施例4] 実施例4では、耐薬品および耐酸化を考慮した金属複合
部品を製造する。この場合には、合せ材として、ステン
レス(例えば、SUS304)、インコネル等が考えら
れるが、ここでは、厚さ0.2mmのSUS304板材
を用意した。一方、基材には、軽量化に好ましいAl−
Si合金(例えば、Si分散合金として熱膨張係数1
3.5×10-6/K、熱伝導率0.30cal/cm・
sec・℃、密度2.53g/cm3 、Hv110の材
料である商品名CMSH A40)から成る厚さ1.6
mmの板材を用意した。基材には、実施例3と同様な亜
鉛置換法により、全面5μmの包みNiめっきを施し
た。さらに、実施例3と同様な方法として、40%Sn
−Pbはんだにより300℃でろう付け(接合)し、S
US304/Al−Si合金(CMSH A40)/SUS30
4の3層グラッド複合材を得た。Example 4 In Example 4, a metal composite part is manufactured in consideration of chemical resistance and oxidation resistance. In this case, stainless steel (for example, SUS304), Inconel, or the like can be used as the joining material. Here, a SUS304 plate material having a thickness of 0.2 mm is prepared. On the other hand, for the base material, Al-
Si alloy (for example, having a thermal expansion coefficient of 1
3.5 × 10 −6 / K, thermal conductivity 0.30 cal / cm ·
sec. ° C., density 2.53 g / cm 3 , Hv110, trade name CMSH A40), thickness 1.6
mm plate material was prepared. The substrate was plated with 5 μm-wide wrapped Ni by the same zinc substitution method as in Example 3. Furthermore, as a method similar to the third embodiment, 40% Sn
-Pb solder at 300 ° C (joining), S
US304 / Al-Si alloy (CMSH A40) / SUS30
4 was obtained.
【0032】この熱特性としては、熱膨張係数18.9
×10-6/K、熱伝導率0.54cal/cm・sec
・℃、密度はアルミナと同等の3.60g/cm3 とな
り、表層の耐蝕性、耐酸化性の優れた材料となり、放熱
基板以外の用途も期待できる。The thermal characteristics include a thermal expansion coefficient of 18.9.
× 10 −6 / K, thermal conductivity 0.54 cal / cm · sec
-The temperature and the density are 3.60 g / cm 3 , which is equivalent to that of alumina, and the material is excellent in corrosion resistance and oxidation resistance of the surface layer.
【0033】[実施例5]基材として、厚さ0.2mm
のMo板を用意し、合せ材として厚さ10mmの純Al
板を用意した。Example 5 As a substrate, a thickness of 0.2 mm
Mo plate is prepared, and pure Al with a thickness of 10 mm is used as a bonding material.
A board was prepared.
【0034】Mo板は、電解Niめっきにより、Niを
2μm被覆させ、水素気流中で800℃で熱処理を行な
いMo/Niの密度強度を充分向上させた。Al板は、
実施例3同様の亜鉛置換法により、Niを2μm包みめ
っきした。The Mo plate was coated with 2 μm of Ni by electrolytic Ni plating, and heat-treated at 800 ° C. in a hydrogen stream to sufficiently improve the density strength of Mo / Ni. Al plate is
By the same zinc substitution method as in Example 3, Ni was wrapped and plated at 2 μm.
【0035】これをMo/Al/Mo、3層形態になる
べく重ね合せた後、加熱温度を400℃で熱間圧延によ
り、総厚換算約60%の加工率を施した。その結果とし
て、Mo部0.18mm、Al部4mmの層厚のクラッ
ド複合材となった。After this was superposed to form a three-layered structure of Mo / Al / Mo, a working rate of about 60% in terms of total thickness was applied by hot rolling at a heating temperature of 400 ° C. As a result, a clad composite material having a Mo part of 0.18 mm and an Al part of 4 mm was obtained.
【0036】このようにして得られた複合材は、熱膨張
率13.2×10-6/K、熱伝導率0.24cal/c
m・sec・℃、密度3.0g/cm3 を有していた。
また、この複合材では、Moが表面第一層に位置し、し
かも基材を挟んでいるため、高強度の求められる複合材
へも適用可能となった。The composite material thus obtained has a coefficient of thermal expansion of 13.2 × 10 −6 / K and a thermal conductivity of 0.24 cal / c.
m · sec · ° C. and density 3.0 g / cm 3 .
Further, in this composite material, Mo is located in the first layer on the surface and sandwiches the base material, so that it can be applied to a composite material requiring high strength.
【0037】また、Alにめっきを施さずとも、必要に
応じてMoに本例の強固なNi被覆をした上、爆発圧着
によりAl表層の酸化物層を除去しながら接合し、圧延
により仕上げを施すことによっても、上に述べた実施例
と同等の3層形態から成る複合材を得る事が出来る。Further, even if Al is not plated, Mo is coated with the strong Ni of the present example as required, and then joined by removing the oxide layer of the Al surface layer by explosion pressure bonding and finishing by rolling. By applying the same, it is possible to obtain a composite material having a three-layer configuration equivalent to that of the above-described embodiment.
【0038】尚、以上説明した実施例によるクラッド複
合材はいずれも、接合界面の密着強度が所望レベルを達
成しており、性能安定な基板として使用可能であること
も確認できた。It was also confirmed that the clad composite materials according to the above-described embodiments all achieved a desired level of adhesion strength at the bonding interface, and could be used as a substrate having stable performance.
【0039】この様に、放熱基板の実質的な軽量化と熱
的特性を鑑みて作製することで、クラッドの金属複合部
品としてパッケージに組み込み、市場の各々の設計事情
により異なる仕様に対し満足するものが得られる様にな
った。In this way, by taking into account the substantial weight reduction and thermal characteristics of the heat dissipation substrate, it is incorporated into a package as a clad metal composite component, and satisfies different specifications depending on each design situation in the market. Things can now be obtained.
【0040】また、以上説明した本発明による金属複合
部品は、セラミックパッケージ用の放熱基板の他に、リ
ードフレーム等周辺部品が高熱膨張のものでその材料と
の熱的整合性を重視すると共に、プラスチックパッケー
ジの採用が進む中で特に軽量性を重視する接合に応える
必要のある部材に適用できる。このことは、パッケージ
の設計上有用なことといえる。In the metal composite component according to the present invention described above, in addition to the heat dissipation board for the ceramic package, the peripheral components such as the lead frame have a high thermal expansion, and the thermal compatibility with the material is emphasized. It can be applied to members that need to respond to joining where importance is placed on weight especially as the use of plastic packages progresses. This is useful in designing a package.
【0041】[0041]
【発明の効果】以上説明したように、本発明による金属
複合部品は、軽量化の要求に応え得ると共に、熱膨張係
数、熱伝導率の点でも十分な特性を有している。As described above, the metal composite part according to the present invention can meet the demand for weight reduction and has sufficient characteristics in terms of thermal expansion coefficient and thermal conductivity.
───────────────────────────────────────────────────── フロントページの続き (51)Int.Cl.6 識別記号 庁内整理番号 FI 技術表示箇所 H01L 23/373 (72)発明者 有川 正 富山県富山市岩瀬古志町2番地 東京タ ングステン株式会社富山製作所内 (72)発明者 氏本 泰弘 福岡県筑紫野市大字山家5447番地 旭化 成工業株式会社内 (72)発明者 松下 忠美 福岡県筑紫野市大字山家5447番地 旭化 成工業株式会社内 (72)発明者 小林 聡 東京都千代田区内幸町1丁目1番地1号 旭化成工業株式会社内 (56)参考文献 特開 平1−118435(JP,A) 特開 昭63−261863(JP,A) 特開 平2−187285(JP,A) 特開 昭64−36440(JP,A)──────────────────────────────────────────────────続 き Continued on the front page (51) Int.Cl. 6 Identification code Agency reference number FI Technical indication location H01L 23/373 (72) Inventor Tadashi Arikawa 2nd Iwase Koshimachi, Toyama City, Toyama Pref. Tokyo Tungsten Co., Ltd. Inside the Toyama Works (72) Inventor Yasuhiro Ujimoto 5447 Oji Yamaji, Chikushino-shi, Fukuoka Asahi Kasei Kogyo Co., Ltd. (72) Inventor Satoshi Kobayashi 1-1, Uchisaiwai-cho, Chiyoda-ku, Tokyo Asahi Kasei Kogyo Co., Ltd. (56) References JP-A-1-118435 (JP, A) JP-A-63-261863 (JP, A) JP-A-2-187285 (JP, A) JP-A-64-36440 (JP, A)
Claims (4)
れた少くとも一層の合せ材とにより構成される金属複合
部品において、前記基材は、モリブデンおよびアルミニ
ウム/シリコン合金のうちのどちらか一方であり、前記
合せ材は、前記基材がモリブデンの場合には、ステンレ
ス、インバー、インコネル、およびチタンのうちから選
ばれた少くとも1種であり、前記基材がアルミニウム/
シリコン合金の場合には、銅、アルミニウム、ステンレ
ス、インバー、インコネル、およびチタンのうちから選
ばれた少くとも1種であり、前記基材および前記合せ材
は、爆発圧着工程またはろう付け工程を含む工程により
接合されており、複合部品全体の熱膨脹係数が10.0
×10-6 /Kよりも大きく23.0×10-6 /Kよりも
小さい範囲にあり、かつ、(前記合せ材の層厚/前記基
材の層厚)で定義される層厚比が3/1乃至9/1であ
ることを特徴とする金属複合部品。1. A metal composite component comprising at least one substrate and at least one bonding material joined to the substrate, wherein the substrate comprises molybdenum and an aluminum / silicon alloy. When the base material is molybdenum , the bonding material is a stainless steel.
Steel, Invar, Inconel, and titanium.
At least one kind of base material, wherein the base material is aluminum /
In the case of silicon alloy, copper, aluminum, stainless steel
Steel, Invar, Inconel, and titanium.
The base material and the composite material are joined by a process including an explosion pressure bonding process or a brazing process, and the thermal expansion coefficient of the entire composite component is 10.0.
The layer thickness ratio is greater than × 10 −6 / K and less than 23.0 × 10 −6 / K , and the layer thickness ratio defined by (layer thickness of the composite material / layer thickness of the base material) A metal composite part having a ratio of 3/1 to 9/1.
乃至15.0×10-6 /Kであることを特徴とする請求
項1に記載の金属複合部品。2. The thermal expansion coefficient is 13.0 × 10 −6 / K.
2. The metal composite part according to claim 1, wherein the ratio is 15.0 × 10 −6 / K. 3.
ことを特徴とする請求項1または2に記載の金属複合部
品。3. The metal composite component according to claim 1, wherein a plating layer is provided on a surface of the composite material.
に、めっき層を有することを特徴とする請求項1乃至3
のいずれかに記載の金属複合部品。4. A plating layer is provided on a boundary surface between the base material and the bonding material in contact with the base material.
A metal composite part according to any one of the above.
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP5164516A JP2717918B2 (en) | 1993-07-02 | 1993-07-02 | Metal composite parts |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP5164516A JP2717918B2 (en) | 1993-07-02 | 1993-07-02 | Metal composite parts |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| JPH0716981A JPH0716981A (en) | 1995-01-20 |
| JP2717918B2 true JP2717918B2 (en) | 1998-02-25 |
Family
ID=15794654
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP5164516A Expired - Lifetime JP2717918B2 (en) | 1993-07-02 | 1993-07-02 | Metal composite parts |
Country Status (1)
| Country | Link |
|---|---|
| JP (1) | JP2717918B2 (en) |
Families Citing this family (3)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JP5428520B2 (en) * | 2009-05-21 | 2014-02-26 | 住友電気工業株式会社 | LED element and method for manufacturing LED element |
| CN103252572B (en) * | 2013-05-10 | 2015-02-04 | 山东大学 | Transient liquid phase diffusion bonding process of molybdenum copper alloy and stainless steel |
| JP7329370B2 (en) * | 2018-06-21 | 2023-08-18 | Jfe精密株式会社 | Heat sink and its manufacturing method |
Family Cites Families (4)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JPS63261863A (en) * | 1987-04-20 | 1988-10-28 | Hitachi Cable Ltd | Surface mounting board |
| JPS6436440A (en) * | 1987-08-01 | 1989-02-07 | Hitachi Cable | Clad material for electronic components |
| JPH01118435A (en) * | 1987-10-31 | 1989-05-10 | Tokyo Tungsten Co Ltd | Composite material of aluminum and molybdenum and manufacture thereof |
| JP2717832B2 (en) * | 1989-01-12 | 1998-02-25 | 東京タングステン株式会社 | Composite metal material and its manufacturing method |
-
1993
- 1993-07-02 JP JP5164516A patent/JP2717918B2/en not_active Expired - Lifetime
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| Publication number | Publication date |
|---|---|
| JPH0716981A (en) | 1995-01-20 |
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