JPS5844712A - Heat treatment device for semiconductor - Google Patents
Heat treatment device for semiconductorInfo
- Publication number
- JPS5844712A JPS5844712A JP14294681A JP14294681A JPS5844712A JP S5844712 A JPS5844712 A JP S5844712A JP 14294681 A JP14294681 A JP 14294681A JP 14294681 A JP14294681 A JP 14294681A JP S5844712 A JPS5844712 A JP S5844712A
- Authority
- JP
- Japan
- Prior art keywords
- reactor
- compound
- sample stage
- capillary tube
- inert gas
- 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
- 238000010438 heat treatment Methods 0.000 title claims abstract description 23
- 239000004065 semiconductor Substances 0.000 title claims description 11
- 150000001875 compounds Chemical class 0.000 claims abstract description 15
- 238000010494 dissociation reaction Methods 0.000 claims abstract description 10
- 230000005593 dissociations Effects 0.000 claims abstract description 10
- 239000011261 inert gas Substances 0.000 claims abstract description 8
- 238000006243 chemical reaction Methods 0.000 claims description 10
- XUIMIQQOPSSXEZ-UHFFFAOYSA-N Silicon Chemical compound [Si] XUIMIQQOPSSXEZ-UHFFFAOYSA-N 0.000 claims description 4
- 229910052710 silicon Inorganic materials 0.000 claims description 4
- 239000010703 silicon Substances 0.000 claims description 4
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 claims description 3
- 229910052799 carbon Inorganic materials 0.000 claims description 3
- -1 gallium arsenide (GaAs) compound Chemical class 0.000 claims description 2
- 238000007599 discharging Methods 0.000 claims 1
- 239000000178 monomer Substances 0.000 claims 1
- 238000007669 thermal treatment Methods 0.000 claims 1
- 239000000758 substrate Substances 0.000 abstract description 23
- 239000007789 gas Substances 0.000 abstract description 14
- 229910001218 Gallium arsenide Inorganic materials 0.000 abstract description 13
- 239000012535 impurity Substances 0.000 abstract description 5
- 239000000376 reactant Substances 0.000 abstract description 4
- 238000000137 annealing Methods 0.000 abstract description 3
- JBRZTFJDHDCESZ-UHFFFAOYSA-N AsGa Chemical compound [As]#[Ga] JBRZTFJDHDCESZ-UHFFFAOYSA-N 0.000 description 9
- 238000000034 method Methods 0.000 description 5
- 230000003647 oxidation Effects 0.000 description 4
- 238000007254 oxidation reaction Methods 0.000 description 4
- XKRFYHLGVUSROY-UHFFFAOYSA-N Argon Chemical compound [Ar] XKRFYHLGVUSROY-UHFFFAOYSA-N 0.000 description 3
- 229910052751 metal Inorganic materials 0.000 description 3
- 239000002184 metal Substances 0.000 description 3
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 description 2
- 229910052785 arsenic Inorganic materials 0.000 description 2
- RQNWIZPPADIBDY-UHFFFAOYSA-N arsenic atom Chemical compound [As] RQNWIZPPADIBDY-UHFFFAOYSA-N 0.000 description 2
- 238000005468 ion implantation Methods 0.000 description 2
- 150000002500 ions Chemical class 0.000 description 2
- 238000004519 manufacturing process Methods 0.000 description 2
- 239000002362 mulch Substances 0.000 description 2
- 230000001681 protective effect Effects 0.000 description 2
- 230000003213 activating effect Effects 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
- 229910052786 argon Inorganic materials 0.000 description 1
- 150000001495 arsenic compounds Chemical class 0.000 description 1
- 238000011109 contamination Methods 0.000 description 1
- 238000001816 cooling Methods 0.000 description 1
- 238000010586 diagram Methods 0.000 description 1
- 238000009826 distribution Methods 0.000 description 1
- 230000000694 effects Effects 0.000 description 1
- 238000002474 experimental method Methods 0.000 description 1
- 239000003779 heat-resistant material Substances 0.000 description 1
- 238000002347 injection Methods 0.000 description 1
- 239000007924 injection Substances 0.000 description 1
- 230000014759 maintenance of location Effects 0.000 description 1
- 239000000463 material Substances 0.000 description 1
- 150000004767 nitrides Chemical class 0.000 description 1
- 230000003287 optical effect Effects 0.000 description 1
- 230000001590 oxidative effect Effects 0.000 description 1
- 239000000843 powder Substances 0.000 description 1
- 238000003825 pressing Methods 0.000 description 1
- 230000002250 progressing effect Effects 0.000 description 1
- 239000010453 quartz Substances 0.000 description 1
- 238000010581 sealed tube method Methods 0.000 description 1
- 150000003377 silicon compounds Chemical class 0.000 description 1
- 229910052814 silicon oxide Inorganic materials 0.000 description 1
- 239000000126 substance Substances 0.000 description 1
- 238000006467 substitution reaction Methods 0.000 description 1
Classifications
-
- H—ELECTRICITY
- H01—ELECTRIC ELEMENTS
- H01L—SEMICONDUCTOR DEVICES NOT COVERED BY CLASS H10
- H01L21/00—Processes or apparatus adapted for the manufacture or treatment of semiconductor or solid state devices or of parts thereof
- H01L21/02—Manufacture or treatment of semiconductor devices or of parts thereof
- H01L21/04—Manufacture or treatment of semiconductor devices or of parts thereof the devices having potential barriers, e.g. a PN junction, depletion layer or carrier concentration layer
- H01L21/18—Manufacture or treatment of semiconductor devices or of parts thereof the devices having potential barriers, e.g. a PN junction, depletion layer or carrier concentration layer the devices having semiconductor bodies comprising elements of Group IV of the Periodic Table or AIIIBV compounds with or without impurities, e.g. doping materials
- H01L21/26—Bombardment with radiation
- H01L21/263—Bombardment with radiation with high-energy radiation
- H01L21/265—Bombardment with radiation with high-energy radiation producing ion implantation
Landscapes
- Physics & Mathematics (AREA)
- High Energy & Nuclear Physics (AREA)
- Engineering & Computer Science (AREA)
- Health & Medical Sciences (AREA)
- Toxicology (AREA)
- Condensed Matter Physics & Semiconductors (AREA)
- General Physics & Mathematics (AREA)
- Manufacturing & Machinery (AREA)
- Computer Hardware Design (AREA)
- Microelectronics & Electronic Packaging (AREA)
- Power Engineering (AREA)
- Crystals, And After-Treatments Of Crystals (AREA)
Abstract
Description
【発明の詳細な説明】
°本発明は化合物半導体の製造装置、より詳しくは不純
物をイオン注入したガリウム・ヒ素(Gaム一)半導体
基板を活性化するための熱処理装置に関する。DETAILED DESCRIPTION OF THE INVENTION The present invention relates to a compound semiconductor manufacturing apparatus, and more particularly to a heat treatment apparatus for activating a gallium arsenide (Ga) semiconductor substrate into which impurity ions have been implanted.
化金物半導体の一つであるGaAs 半導体は、シリ
コン半導体に比べて電子移動度が大きいために注目され
′Cおり、すでに光半都素子やマイク−波素子として実
用化されている。かかるGaムS 半導体製造ブーセス
の中で行われる不純物ドーピングの技術としCは、一般
KjL好な不純物分布が得られることや再現性の良さか
らイオン注入法が利用されているが、従来の方法による
場合には、イオン注入1ktca@を活性化させる必要
があり、そのためK 800℃以上の高温で熱部II(
アニール)を行なわなければならない、しかしながら、
GaムS 化合物は解離圧が大きいために1通常の炉7
二−ルを行なったのではヒ素(ムS)が解離してしまい
。GaAs semiconductors, which are one of the chemical compound semiconductors, have attracted attention because of their higher electron mobility than silicon semiconductors, and have already been put to practical use as optical halftone devices and microphone wave devices. As the impurity doping technology carried out in the semiconductor manufacturing process, the ion implantation method is generally used because it can obtain a good impurity distribution and has good reproducibility. In some cases, it is necessary to activate the ion implantation 1ktca@, and therefore the thermal part II (
However,
Because the GaM S compound has a large dissociation pressure, it is
If the arsenic was used, the arsenic (S) would dissociate.
また酸化などの問題も発生する。かかる解離や酸化など
を防止するために、従来技術においては7二−ルに種々
の工夫をなしてきた。Problems such as oxidation also occur. In order to prevent such dissociation and oxidation, various improvements have been made to 7-diyl in the prior art.
例えば、保鏝膜を利用して行う保t!kM7二−ルの方
法においては、不純物イオン注入後のGaps基板上に
シリコン酸化物(810m)、シリコ/窒化Qkt (
811N4 )などの保護膜を形成し、しかる俵にア
ニールを行っているが、かかる方法によって一ム畠 の
解離は完全には避けられず、またりpム(Cr)をドー
ピングしている半絶縁性GaAs 基板tは、Cr
が保Ii膜に吸着される現象が起こり。For example, using a protective trowel! kM7 In Neel's method, silicon oxide (810 m), silicon/nitride Qkt (
A protective film such as 811N4) is formed and the bales are annealed, but this method cannot completely avoid the dissociation of Ichimuhatake, and semi-insulating films doped with PM (Cr) The GaAs substrate t is Cr
A phenomenon occurs in which is adsorbed to the retention Ii film.
さらには、GaA−基板と保m腺との熱膨張係数の差に
よりストレスが発生し、イオン注入層の性質が変化する
という難点がある。Furthermore, there is a problem that stress is generated due to the difference in thermal expansion coefficient between the GaA-substrate and the thermal expansion layer, which changes the properties of the ion-implanted layer.
また、同一管内K GaA−基板と金属ムl を封じ込
んで7二−ルする閉管法(または封管法)の場゛ 合
には、金属ムI から出るム1 圧の・制御が―かしい
上に、冷却時にム易 がGaAs 基板表面や管内壁
に凝着して汚染し、さらKはその取り扱いも離しいとい
5間層がある。In addition, in the case of a closed tube method (or sealed tube method) in which a KGaA substrate and a metal layer are sealed in the same tube for 7 hours, it is difficult to control the pressure of the layer released from the metal layer. On top of this, there is a five-layer layer that adheres to the surface of the GaAs substrate and the inner wall of the tube during cooling and contaminates it, while K is difficult to handle.
本発明・工、GaA−基板を800 ”C以上で7ニー
ルす1wK11lして問題となるムlの解離と酸化を防
止するために、アニール温度においてGaAs 化合
物よりも解離圧の高いム1 化合物を同一反応系中に置
き、そのム龜圧によってGaAs 基板弐藺からのム1
の解離を防ごうとするものであり、*9mいも簡単で
操作上の危険も少なく、かつ再現性のよい熱処理装置を
提供するものである。In the present invention, in order to prevent the dissociation and oxidation of mulch, which is a problem when a GaA-substrate is annealed at 800"C or higher for 7 days, a mulch compound having a higher dissociation pressure than a GaAs compound at the annealing temperature is used. Placed in the same reaction system, the pressure from the GaAs substrate increases
The purpose is to provide a heat treatment apparatus that is simple, has little operational risk, and has good reproducibility.
以下1本発明の実施例を添付図面にもとづいて説明する
。An embodiment of the present invention will be described below with reference to the accompanying drawings.
添付図面は本発明にがかる熱処理装置を模式図的に示し
たものであるが1本装置・工大きく分けると反応装置、
加熱装置ならびに雰囲気#I411の配管制御系から構
成される0反応装置1は、上部にふた2をすり合わせ【
密閉mK影形成れ、その内部ニハ試料台3を設け、絨試
料台3の下面には熱電対4をその先端が接触するように
配設する。ここで、反応装置lは、一般には石英製であ
るが、アルミナ(ムl*Oa ) 、カーボンあるいは
他の耐熱材料な使用してもよく、またふた2&工その自
重によっても気密性が保たれるように比較的大11Kか
つ重い材料で設計され【いるが、さらにその気密性を高
めるぺ(1例えば重りやバネ等を利用して加圧するよう
にし、または保合部に溝を形成して多重に突き合わせる
ようにしてもよ〜・。The attached drawings schematically show the heat treatment apparatus according to the present invention.
The reactor 1, which consists of a heating device and a piping control system for atmosphere #I411, is equipped with a lid 2 on the top [
A sealed mK shadow is formed, and a nimate sample stage 3 is provided inside the mK, and a thermocouple 4 is disposed on the lower surface of the carpet sample stage 3 so that its tip is in contact with it. Here, the reactor 1 is generally made of quartz, but may also be made of alumina (mul*Oa), carbon, or other heat-resistant materials, and the lid 2 & It is designed with a relatively large 11K and heavy material so that it can be held in place, but it is possible to further increase the airtightness by applying pressure using weights, springs, etc., or by forming grooves in the retaining part. You can try matching multiple times.
反応装置lの一方側面に不活性ガス畝入用の第1の毛管
5を1反対側面に排気用の第2の毛管「を取り付け、さ
らに第1の毛管50過中にムl 圧調整用の第3の毛管
6を取り付け、それぞれの毛管には反応装置l内のガス
を置換したり、ガス圧を調整するための第1のコック7
.第2のコック8および第3のフック9を設けである。A first capillary tube 5 for inert gas injection is attached to one side of the reactor, and a second capillary tube for exhaust gas is attached to the opposite side. A third capillary tube 6 is attached to each capillary tube, and each capillary tube has a first cock 7 for displacing the gas in the reactor l and adjusting the gas pressure.
.. A second cock 8 and a third hook 9 are provided.
ここで毛管を使用した理由tX、管内のガス逆流を防止
するのに効果があるためである。なお5図中、10゜1
σは流量針を、11は圧力針をそれぞれ表わす・加熱装
置としては1反応装置全体を外熱式に加熱するための抵
抗加熱炉12を設け、これを移動可能とし、加熱時には
それを図中白抜き矢印の方向へ移動させる。The reason for using a capillary tube here is that it is effective in preventing gas backflow within the tube. In addition, in Figure 5, 10°1
σ represents a flow rate needle, and 11 represents a pressure needle. As a heating device, a resistance heating furnace 12 is provided to externally heat the entire reactor, and this is movable. During heating, it is shown in the figure. Move it in the direction of the white arrow.
以上の構成により、まず反応装置1内の試料台3上に不
純物イオン注入を終えたGaAm基板13と反応剤とし
てのヒ嵩シ替コン化合物(ム畠81 )14の粉末を載
せ、次に第1のコック7と5Hzのブック8を開き、第
3のコック9を開いて第1の毛管器の一端からアルゴン
(ムr)などの不活性ガスを流し込み(図中実線矢印方
向)1反応装置1内をムr ガスで装置する。前記のよ
うにしてGaAa基板の酸化を防いだ上で、続いて加熱
炉12を反応装置1をカバーする位置まで移動しC図中
白抜き矢印方向)、昇温をll始する。ここで1反応剤
とL℃のムsgi 化合物は700℃以上においてG
aAs化合物の平衡ムl 圧よりも高いムS 圧を発生
するので、 GaA璽 基板の7工−ル温度(850℃
)に達する以前に、まず第2のコック8を閉じてムS
ガスが外へ流出しないようにし、絖い?g3のコック9
及び第1のブック7の開度な調節しながら反応装置1内
のム一 圧を所定の圧力に調整し、場合によってはvI
!i1のプツクフを閉じて第3のブック9の一度のみに
よってム−圧の調整を行う。With the above configuration, first, the GaAm substrate 13 that has been implanted with impurity ions and the powder of the bulk silicon compound (Muhata 81) 14 as a reactant are placed on the sample stage 3 in the reaction apparatus 1, and then the Open the first cock 7 and the 5Hz book 8, open the third cock 9, and pour inert gas such as argon (Mr) from one end of the first capillary device (in the direction of the solid line arrow in the figure). The inside of the chamber is equipped with murium gas. After preventing the GaAa substrate from oxidizing as described above, the heating furnace 12 is then moved to a position covering the reaction apparatus 1 (in the direction of the white arrow in Fig. C), and temperature rise is started. Here, 1 reactant and the musgi compound at L°C are G at 700°C or higher.
Since it generates a S pressure higher than the equilibrium S pressure of the aAs compound, the temperature of the GaA substrate (850°C) is
), close the second cock 8 and press
Make sure the gas doesn't leak out, and put it on. g3 cook 9
The pressure inside the reactor 1 is adjusted to a predetermined pressure while adjusting the opening degree of the first book 7, and depending on the case, vI is adjusted to a predetermined pressure.
! After closing the push button i1, the pressure is adjusted only once using the third book 9.
アニール終了後(工、まず第2のコック8を開き第3の
ブック9を閉じて謳1のコック7を開き温度降下にしま
たがって除々に反応装置l内をムr ガスで置換する。After the annealing is completed, first open the second cock 8, close the third book 9, open the first cock 7, and gradually replace the inside of the reactor 1 with the gas while the temperature drops.
この際、ムr ガスの置換適度には十分注意する必要が
あり、例えば温度がまだ高いうちK(ム― の解離が進
行している温度範囲で)急激に置換すると、 GaAs
基板からム−が解離する危険性があり、逆に低温ま
で置換が完了しない場合にはム1 ガスが凝着して、G
aム廖 基板弐画を汚染し【しまう危険性がある。した
がって、あらかじめ実験によって操作条件をよくつかん
でおく必要がある。At this time, it is necessary to be careful about the appropriateness of the substitution of the mu gas. For example, if K is replaced rapidly while the temperature is still high (in the temperature range where the dissociation of mu gas is progressing), GaAs
There is a risk that Mu1 will dissociate from the substrate, and on the other hand, if the replacement is not completed until the temperature reaches a low temperature, Mu1 gas will adhere and G
There is a risk of contaminating the printed circuit board. Therefore, it is necessary to thoroughly understand the operating conditions through experiments in advance.
なお1本実施例においては、反応剤とし【ムー81化合
物を用いたが、使用する温度領域においてG1ム龜 化
合物の平衝ムS 圧よりも高いム膳 圧を発生す番物質
であれば伺を使用してもよい。In this example, a compound [Mu81] was used as a reactant, but any substance that generates a pressure higher than the equilibrium pressure of the G1 compound in the temperature range used may be used. may be used.
また他の実施例においては、加熱方式に高周波加熱を試
みた。すなわち1反応装置内にカーボン製の試料台を設
け、骸試料台上にGaム一 基板とム−81化合物を載
せ、高周波加熱を行うものであ番が、このg GaAs
化合物を載せる試料台とムm81化合物を載せる試
料台の形状と寸法を適宜設定し。In other examples, high frequency heating was tried as a heating method. In other words, a carbon sample stage is provided in one reaction device, a GaAs substrate and a Mu-81 compound are placed on the skeleton specimen stage, and high frequency heating is performed.
The shape and dimensions of the sample stand on which the compound is placed and the sample stand on which the m81 compound is placed are set appropriately.
昇温速度や到達温度などの加熱特性を制御することが可
能であり、さらKJL好な結果を得ることができた。It was possible to control the heating characteristics such as the rate of temperature increase and the temperature reached, and even better results could be obtained with KJL.
本発明は1以上設明したように、同一反応装置内KGa
AsJll+板と眩GaAs 基板よりも平衡・ムS
圧の高いヒ素化合物とを入れてアニールするので。The present invention provides one or more KGa in the same reactor as established.
AsJll+ plate and dazzling GaAs substrate, equilibrium and mu S
Because it is annealed by adding a high-pressure arsenic compound.
GaAs 基板からのム謬 の解離が防止でき、しかも
金属ム畠 を使用する場合のように大量のム−ガスの発
生がないので危険が少なく、例えば長時間7エールが可
能になるなど熱処理の自由度も増し、さらKは咄管を利
用して雰囲気−、整をするので再iI性がよ(、ま−た
不活性ガスをうまく利用して酸化やム−ガスによる汚染
も防止することができるのt、そのおよばず効果昏工非
常に大きなものである。It is possible to prevent the dissociation of gas from the GaAs substrate, and there is no danger of generating a large amount of gas, unlike when using a metal substrate, and there is less danger in heat treatment, for example, it is possible to conduct heat treatment for a long time. As the temperature increases, SaraK uses a pipe to prepare the atmosphere, making it more reusable (and also making good use of inert gas to prevent oxidation and mu gas contamination). Although it is possible, the effect is extremely large.
図は本発明にかかる熱処理装置の模式図である
1・・・反応装置、2・・・ふた、3・・・試料台。
4・・・熱電対、5 v 5’ e 6・・・毛管、7
98 # 9・・・コック、to、1σ・・・流量針。
11・・・圧力針、12・・・加熱炉、13−Gaムー
基板、14・・・ムー81化合物特許出願人 富士通株
式金社The figure is a schematic diagram of a heat treatment apparatus according to the present invention. 1... Reactor, 2... Lid, 3... Sample stand. 4...Thermocouple, 5 v 5' e 6... Capillary, 7
98 #9...cock, to, 1σ...flow rate needle. DESCRIPTION OF SYMBOLS 11... Pressure needle, 12... Heating furnace, 13-Ga Mu substrate, 14... Mu81 compound patent applicant Fujitsu Ltd. Kinsha
Claims (3)
体の熱処理装置にして、ふたを係合してなる密閉截の反
応装置を設け、該反応装置の内部には試料台と熱電対を
配設し、前記反応装置の相対する両側にはそれぞれ不活
性ガスを導入し排出する毛管を接続し、不活性ガス導入
用毛管には調圧用の他の毛管を接続し、各毛管にはそれ
ぞれフックな取り付け。 一方前記反応装置を覆う加熱炉を移動可能に設けたこと
を特徴とする半導体の熱九層装置。(1) A heat treatment apparatus for gallium arsenide (GaAs) compound semiconductors is provided with a hermetically sealed reaction apparatus having an engaged lid, a sample stage and a thermocouple are disposed inside the reaction apparatus, and a sample stage and a thermocouple are disposed inside the reaction apparatus. Capillaries for introducing and discharging inert gas are connected to opposite sides of the device, and the capillary for introducing inert gas is connected to another capillary for pressure regulation, and each capillary is attached with a hook. On the other hand, a semiconductor thermal nine-layer device, characterized in that a heating furnace covering the reaction device is movably provided.
aム―化合物よりも平衡解離圧の高いし素化合物を同時
にの甘る試料台を設け、熱部理過8におい曵適宜゛不活
性ガスを前記反応装置内に導入するも管を設けたことを
特徴とする特許請求の範囲11111項記載の半導体熱
熟思装置。(2) Inside the reactor, Ga moo & plate, G
A sample stage was provided to simultaneously hold the monomer compound, which has a higher equilibrium dissociation pressure than the mono-compound, and a pipe was provided to introduce an inert gas into the reaction apparatus as appropriate during the thermal treatment 8. A semiconductor mulling device according to claim 11111, characterized in that:
イ素で形成し、該反応装置の外sK・工前記試料台を加
熱する高周波電力発生装置が設けられたことを特徴とす
る特許請求の範囲11111項記載の半導体の熱処理装
置。(3) A patent claim characterized in that the sample stage in the skeleton reaction scissors is made of carbon or silicon-based silicon, and a high-frequency power generator is provided to heat the sample stage outside the reactor. A semiconductor heat treatment apparatus according to item 11111.
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP14294681A JPS5844712A (en) | 1981-09-10 | 1981-09-10 | Heat treatment device for semiconductor |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP14294681A JPS5844712A (en) | 1981-09-10 | 1981-09-10 | Heat treatment device for semiconductor |
Publications (2)
Publication Number | Publication Date |
---|---|
JPS5844712A true JPS5844712A (en) | 1983-03-15 |
JPH0119266B2 JPH0119266B2 (en) | 1989-04-11 |
Family
ID=15327320
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
JP14294681A Granted JPS5844712A (en) | 1981-09-10 | 1981-09-10 | Heat treatment device for semiconductor |
Country Status (1)
Country | Link |
---|---|
JP (1) | JPS5844712A (en) |
Cited By (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US5739263A (en) * | 1992-06-04 | 1998-04-14 | Sumitomo Bakelite Company Limited | Film adhesive and process for production thereof |
-
1981
- 1981-09-10 JP JP14294681A patent/JPS5844712A/en active Granted
Cited By (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US5739263A (en) * | 1992-06-04 | 1998-04-14 | Sumitomo Bakelite Company Limited | Film adhesive and process for production thereof |
Also Published As
Publication number | Publication date |
---|---|
JPH0119266B2 (en) | 1989-04-11 |
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