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JPH0123554B2 - - Google Patents
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JPH0123554B2 - - Google Patents

Info

Publication number
JPH0123554B2
JPH0123554B2 JP59076657A JP7665784A JPH0123554B2 JP H0123554 B2 JPH0123554 B2 JP H0123554B2 JP 59076657 A JP59076657 A JP 59076657A JP 7665784 A JP7665784 A JP 7665784A JP H0123554 B2 JPH0123554 B2 JP H0123554B2
Authority
JP
Japan
Prior art keywords
oxide film
nickel
layer
electronic component
lead
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
Application number
JP59076657A
Other languages
Japanese (ja)
Other versions
JPS60221585A (en
Inventor
Yutaka Okuaki
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.)
Oki Electric Industry Co Ltd
Original Assignee
Oki Electric Industry Co Ltd
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 Oki Electric Industry Co Ltd filed Critical Oki Electric Industry Co Ltd
Priority to JP59076657A priority Critical patent/JPS60221585A/en
Publication of JPS60221585A publication Critical patent/JPS60221585A/en
Publication of JPH0123554B2 publication Critical patent/JPH0123554B2/ja
Granted legal-status Critical Current

Links

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
    • C23GCLEANING OR DE-GREASING OF METALLIC MATERIAL BY CHEMICAL METHODS OTHER THAN ELECTROLYSIS
    • C23G1/00Cleaning or pickling metallic material with solutions or molten salts
    • C23G1/02Cleaning or pickling metallic material with solutions or molten salts with acid solutions
    • C23G1/10Other heavy metals

Landscapes

  • Chemical & Material Sciences (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • General Chemical & Material Sciences (AREA)
  • Engineering & Computer Science (AREA)
  • Materials Engineering (AREA)
  • Mechanical Engineering (AREA)
  • Metallurgy (AREA)
  • Organic Chemistry (AREA)
  • Weting (AREA)
  • Lead Frames For Integrated Circuits (AREA)
  • ing And Chemical Polishing (AREA)

Description

【発明の詳細な説明】 (技術分野) 本発明は、電子部品に形成された薄いニツケル
層の表面に生成した酸化被膜を取り除く方法に関
する。
TECHNICAL FIELD The present invention relates to a method for removing an oxide film formed on the surface of a thin nickel layer formed on an electronic component.

(従来技術) 従来、IC(Integrated Circuit)や受、発光素
子、あるいはリードスイツチ等の電子部品のパツ
ケージから導出したリードには金メツキが施され
ていた。金メツキは、耐食性が大きく、ハンダと
のぬれ性も良いからである。しかしながら近年、
コスト低減の為、金メツキの代わりにハンダメツ
キが用いられる様になつてきた。金メツキもハン
ダメツキも、通常下地メツキ層としてニツケル薄
膜層を使用するが、ハンダメツキの場合はこれら
電子部品を製造する為の熱処理に耐えられない。
従つてハンダメツキはこれら熱処理工程後に行な
われ、ニツケル薄膜層を露出させたまま熱処理が
行なわれることとなる。
(Prior Art) Conventionally, leads derived from packages of electronic components such as ICs (Integrated Circuits), receivers, light emitting elements, and reed switches have been plated with gold. This is because gold plating has high corrosion resistance and good wettability with solder. However, in recent years,
To reduce costs, solder plating has come to be used instead of gold plating. Both gold plating and solder plating usually use a nickel thin film layer as the base plating layer, but solder plating cannot withstand the heat treatment used to manufacture these electronic components.
Therefore, solder plating is performed after these heat treatment steps, and the heat treatment is performed with the nickel thin film layer exposed.

熱処理工程としては、ICを例とすればICチツ
プをパツケージにダイスボンドする工程、あるい
はパツケージにキヤツプをかぶせる、いわゆるシ
ールする工程がある。これら熱処理工程でニツケ
ル薄膜層には薄い酸化被膜が生成する。酸化被膜
はハンダに対するぬれ性が悪いことや導電性が悪
い等電子部品にとつて好ましくない性質を有する
ので除去しなければならない。
Heat treatment processes include, for example, the process of die-bonding an IC chip to a package, or the process of covering the package with a cap, a so-called sealing process. During these heat treatment steps, a thin oxide film is formed on the nickel thin film layer. The oxide film has undesirable properties for electronic components, such as poor solder wettability and poor conductivity, and must be removed.

ニツケル酸化被膜を除去する方法としては、従
来金属便覧(日本金属学会編)P967の表3・236
に記載された酸洗い液が用いられている。ニツケ
ル酸化被膜が酸により除去されるときの反応は例
えばシユウ酸の場合NiO+(COOH)2→2CO2
H2O+Niである。又、多くのピンホールを有し
ており、このピンホールから浸入した酸がアンダ
ーエツチをして酸化被膜と残りのニツケル層とを
分離させるからである。この様に、ニツケル層表
面の酸化被膜は酸で食刻され、化学的に除去され
る。しかしながら金属層もまた酸により食刻され
るのでニツケル面は粗化される。
Conventional methods for removing nickel oxide films are listed in Table 3 and 236 of the Metal Handbook (edited by the Japan Institute of Metals), page 967.
The pickling solution described in is used. For example, in the case of oxalic acid, the reaction when the nickel oxide film is removed by acid is NiO + (COOH) 2 →2CO 2 +
H2O +Ni. In addition, it has many pinholes, and acid that enters through these pinholes causes underetching and separates the oxide film from the remaining nickel layer. In this way, the oxide film on the surface of the nickel layer is etched with acid and chemically removed. However, since the metal layer is also etched by the acid, the nickel surface becomes rough.

ニツケル酸化被膜はこの様にして取り除く為、
ニツケル層が厚い場合は問題ないが、電子部品の
リードに施されたニツケル薄膜層の様に薄い場合
は問題が生ずる。すなわち、上記酸洗い液やカル
ボン酸等の有機酸のみによる酸化被膜の除去方法
では完全に酸化膜を除去することはできない。反
面、食刻時間を長くしたりして酸化膜を完全に除
去するとニツケル層が薄くなりすぎたり、ニツケ
ル薄膜層がはがされ下層の表面が露出したりす
る。従がつていずれにしてもハンダのぬれ性が悪
い等という欠点を有していた。
To remove the nickel oxide film in this way,
There is no problem if the nickel layer is thick, but problems arise if the nickel layer is thin, such as the thin nickel film layer applied to the leads of electronic components. That is, the oxide film cannot be completely removed by the method of removing the oxide film using only the pickling solution or organic acid such as carboxylic acid. On the other hand, if the oxide film is completely removed by increasing the etching time, the nickel layer becomes too thin, or the nickel thin film layer is peeled off, exposing the surface of the underlying layer. Consequently, in any case, they have had drawbacks such as poor solder wettability.

(発明の目的) 本発明は、以上の様な欠点を解消する為になさ
れたもので、その目的は電子部品に被着されたニ
ツケル層表面に生成した酸化被膜をニツケル層の
食刻深さを小さく留めつつ除去する方法を得るこ
とにある。
(Purpose of the Invention) The present invention has been made to eliminate the above-mentioned drawbacks, and its purpose is to reduce the etching depth of the nickel layer by removing the oxide film formed on the surface of the nickel layer adhered to the electronic component. The objective is to find a way to remove it while keeping it small.

(発明の構成) 本発明は、電子部品のパツケージから導出した
リードに被着され、表面に酸化被膜が生成してい
るニツケル薄膜層から前記酸化被膜を除去する方
法において、 前記電子部品のリードを有機酸液に浸漬する工
程と、その後前記電子部品のリードを過酸化水素
とフツ化アンモニウムを主成分とする化学研磨液
に浸漬する工程とを有することを特徴とするニツ
ケル酸化被膜除去方法である。
(Structure of the Invention) The present invention provides a method for removing an oxide film from a nickel thin film layer that is attached to a lead led out from a package of an electronic component and has an oxide film formed on the surface. A method for removing a nickel oxide film, comprising the steps of immersing the lead in an organic acid solution, and then immersing the lead of the electronic component in a chemical polishing solution containing hydrogen peroxide and ammonium fluoride as main components. .

(実施例) 以下本発明の実施例をICのリード下地層とし
て形成されたニツケルメツキ層の表面に生成した
酸化被膜を例にとつて説明する。第1図は、本発
明の一実施例における断面図である。
(Example) Examples of the present invention will be described below by taking as an example an oxide film formed on the surface of a nickel plating layer formed as a lead underlayer of an IC. FIG. 1 is a sectional view of an embodiment of the present invention.

第1図は2〜3μm厚のニツケルメツキ層1が
形成されたリード2を拡大した断面図である。ニ
ツケルメツキ層1には、大気中の酸素等により酸
化被膜3が生成している。4は、ICパツケージ
5の内部から引き出されたメタライズ層であり、
ここにリード2が銀ロウ6により接着されてい
る。
FIG. 1 is an enlarged cross-sectional view of a lead 2 on which a nickel plating layer 1 with a thickness of 2 to 3 μm is formed. An oxide film 3 is formed on the nickel plating layer 1 due to oxygen in the atmosphere. 4 is a metallized layer pulled out from inside the IC package 5;
The leads 2 are bonded here with silver solder 6.

この酸化被膜3を除去するにはリード2をシユ
ウ酸液に浸漬する。シユウ酸の反応は常温では緩
慢なので、ほぼ沸点近くに加熱して約80℃の温度
に保つとよい。
To remove this oxide film 3, the lead 2 is immersed in an oxalic acid solution. The reaction of oxalic acid is slow at room temperature, so it is best to heat it close to its boiling point and keep it at a temperature of about 80°C.

ここで、下から加熱すると対流により流れが発
生するので液をかきまぜる必要がなく、好都合で
ある。
Here, when heating from below, a flow is generated by convection, so there is no need to stir the liquid, which is convenient.

シユウ酸等の有機酸は、ニツケルメツキ層1を
緩慢に食刻するので、ニツケルメツキ層1の食刻
状態を容易に管理することができる。すなわち、
ニツケルメツキ層1の食刻を不動態である酸化層
がはがれ落ちたところで止めることができる。
尚、シユウ酸に代わる有機酸としては酪酸、酢酸
がある。
Since the organic acid such as oxalic acid etches the nickel plating layer 1 slowly, the etched state of the nickel plating layer 1 can be easily controlled. That is,
Etching of the nickel plating layer 1 can be stopped when the passive oxide layer peels off.
Note that organic acids that can replace oxalic acid include butyric acid and acetic acid.

シユウ酸液処理工程が終了してもニツケルメツ
キ層1には、酸化被膜3が残る。このままシユウ
酸液に浸漬し続けるとニツケルメツキ層1を食刻
し続けるので好ましくない。シユウ酸は等方的エ
ツチングをするからである。その為、次に化学研
磨を行なう。
The oxide film 3 remains on the nickel plating layer 1 even after the oxalic acid solution treatment step is completed. If the nickel plating layer 1 is continued to be immersed in the oxalic acid solution, the nickel plating layer 1 will continue to be etched, which is not preferable. This is because oxalic acid performs isotropic etching. Therefore, chemical polishing is performed next.

化学研磨は、過酸化水素とフツ化アンモニウム
を主成分とする化学研磨剤の50%水溶液に常温で
1.5分程度浸漬することにより行なう。この化学
研磨液は、ニツケルメツキ層1の面に垂直の方向
より面に沿つた方向の食刻速度が大きい為、酸化
被膜3を完全に除去し、表面を研磨することが可
能となる。
Chemical polishing involves applying a 50% aqueous solution of a chemical polishing agent containing hydrogen peroxide and ammonium fluoride as main components at room temperature.
This is done by soaking for about 1.5 minutes. Since this chemical polishing liquid has a higher etching rate in the direction along the surface of the nickel plating layer 1 than in the direction perpendicular to the surface, it is possible to completely remove the oxide film 3 and polish the surface.

次に、シユウ酸液の好ましい濃度について説明
する。第2図はシユウ酸濃度(規定度)とハンダ
歩留のグラフ、第3図はシユウ酸濃度(規定度)
と食刻厚さのグラフである。これらは、いずれも
80℃のシユウ酸に5分間浸漬し、化学研磨を行な
つた後のデーターである。
Next, a preferred concentration of the oxalic acid solution will be explained. Figure 2 is a graph of oxalic acid concentration (normality) and solder yield, Figure 3 is a graph of oxalic acid concentration (normality)
This is a graph of the etching thickness. These are all
This data is after immersion in 80°C oxalic acid for 5 minutes and chemical polishing.

第2図により、ニツケルメツキ層1上にハンダ
メツキをする為には、酸化被膜3を除去する場
合、約1〜3規定が好ましいことがわかる。
From FIG. 2, it can be seen that in order to perform solder plating on the nickel plating layer 1, when removing the oxide film 3, about 1 to 3 normal is preferable.

第3図により、2〜3規定で約1.1μmとなつて
いる。第2図を考えれば規定前後が食刻速度が速
く、歩留りが良く好ましいことがわかる。
According to FIG. 3, it is approximately 1.1 μm under 2 to 3 standards. Considering FIG. 2, it can be seen that the etching speed is fast and the yield is good before and after the specified value.

ところで、シユウ酸を代表する有機酸による食
刻の代わりに、SO4 2-やNO3 -オイン等を含む無
機酸による食刻を行なうと以下の様な問題が生ず
る。それは、パツケージ5の内部には、ICチツ
プが搭載され、アルミ配線がなされているが、ア
ルミニウムはわずかに存在するSO4 2-イオンや
NO3 -イオンとでも極めて反応しやすいので、内
部に浸入してきたこれらイオンと反応してアルミ
断線が生じやすくなるからである。又、リード2
とメタライズ層4とを接着する銀ロウ6に含まれ
る銀はマイグレーシヨンを起こしやすい。
By the way, when etching is performed using an inorganic acid containing SO 4 2- , NO 3 -oin , etc. instead of etching using an organic acid such as oxalic acid, the following problems occur. Inside the package 5, an IC chip is mounted and aluminum wiring is made, but the aluminum contains a small amount of SO 4 2- ions and
This is because it is extremely reactive with NO 3 - ions, and reacts with these ions that have entered the interior, making it easy for aluminum wires to break. Also, lead 2
Silver contained in the silver solder 6 that adheres the metallized layer 4 and the metallized layer 4 is likely to undergo migration.

ニツケルメツキ層1は、このマイグレーシヨン
防止の役割も果している為、無機酸によりニツケ
ルメツキ層1がはがされ、更に、ここにSO4 2-
NO3 -等のイオンが残つていると、銀ロウ6に含
まれる銀は、これらイオンに誘発され、極めてマ
イグレーシヨンが発生しやすくなる。マイグレー
シヨンが発生するとリード間あるいはメタライズ
層間の短絡等、ICにおいて好ましくない現象が
生ずるのである。
Since the nickel plating layer 1 also plays the role of preventing this migration, the nickel plating layer 1 is peeled off by the inorganic acid, and furthermore, SO 4 2- and
If ions such as NO 3 - remain, the silver contained in the silver solder 6 will be induced by these ions, and migration will be extremely likely to occur. When migration occurs, undesirable phenomena occur in the IC, such as short circuits between leads or between metallized layers.

尚、シユウ酸による食刻をしないで、化学研磨
液のみによつてニツケル酸化被膜除去を行なうの
も可能であるが、過酸化水素とフツ化アンモニウ
ムを主成分とする化学研磨液は劣化が速く、この
液だけで酸化被膜除去を行なうとしばしば取り換
える必要が生ずる。この様に取り換えの回数が多
いと、取り換えがわずらわしいだけでなく、化学
研磨液は高価な為に非常なコスト高になるのであ
る。更に、酸化被膜の除去が均一に行なわれずに
むらになつてしまうという欠点も有するのであ
る。
It is also possible to remove the nickel oxide film using only a chemical polishing solution without etching with oxalic acid, but chemical polishing solutions whose main components are hydrogen peroxide and ammonium fluoride deteriorate quickly. If the oxide film is removed using only this solution, it will often be necessary to replace it. If the number of replacements is as high as this, not only is it troublesome to replace, but the chemical polishing liquid is expensive, resulting in an extremely high cost. Furthermore, it also has the disadvantage that the oxide film is not removed uniformly and becomes uneven.

(発明の効果) 以上説明した様に本発明によれば電子部品に被
着され、表面に酸化被膜が生成しているニツケル
薄膜層から、酸化被膜を除去するのに有機酸液に
浸漬し、過酸化水素とフツ化アンモニウムとを主
成分とする化学研磨液に浸漬するので、次の様な
効果がある。
(Effects of the Invention) As explained above, according to the present invention, in order to remove an oxide film from a nickel thin film layer that is adhered to an electronic component and has an oxide film formed on the surface, immersion in an organic acid solution is performed. Since it is immersed in a chemical polishing liquid whose main components are hydrogen peroxide and ammonium fluoride, it has the following effects.

第1に、有機酸によりある程度酸化被膜を除去
し、上記化学研磨液で残りの酸化被膜を完全に取
り去るので、所定のニツケル層厚を残しつつ酸化
被膜を除去することができる様になる。これは、
酸化被膜除去の効率を最大限ならしめるものであ
る。第2に、これら食刻液、研磨液は配像の切断
やマイグレーシヨンを誘発するイオンを含んでい
ないので電子部品の信頼性に影響を及ぼさない。
First, since the oxide film is removed to some extent with the organic acid and the remaining oxide film is completely removed with the chemical polishing liquid, the oxide film can be removed while leaving a predetermined nickel layer thickness. this is,
This maximizes the efficiency of oxide film removal. Second, these etching liquids and polishing liquids do not contain ions that cause image cutting or migration, and therefore do not affect the reliability of electronic components.

第3に、浸漬するだけで良く、相互に絶縁され
たリードを有していて電解研磨ができない形状で
あつても電子部品のリードに形成された酸化被膜
を除去することができる。
Thirdly, it is possible to remove the oxide film formed on the leads of electronic components by simply immersing them, even if the leads of electronic components have mutually insulated leads and cannot be subjected to electrolytic polishing.

本実施例ではICのリードを例にとつて説明し
たが、IC以外でも受、発光ダイオードや、リー
ドスイツチ等、ニツケル薄膜層を有していれば広
く実施することができる。
Although this embodiment has been explained using an IC lead as an example, it can be widely applied to other devices other than ICs, such as receivers, light emitting diodes, reed switches, etc., as long as they have a nickel thin film layer.

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

第1図は本発明のニツケル酸化被膜除去方法の
一実施例の側面図、第2図はシユウ酸濃度とハン
ダ歩留の関係を示す図表、第3図はシユウ酸濃度
と食刻厚さの関係を示す図表である。 1…ニツケルメツキ層、2…リード、3…ニツ
ケル酸化被膜。
Fig. 1 is a side view of an embodiment of the nickel oxide film removal method of the present invention, Fig. 2 is a chart showing the relationship between oxalic acid concentration and solder yield, and Fig. 3 is a graph showing the relationship between oxalic acid concentration and etching thickness. This is a diagram showing the relationship. 1... Nickel plating layer, 2... Lead, 3... Nickel oxide film.

Claims (1)

【特許請求の範囲】 1 電子部品のパツケージから導出したリードに
被着され、表面に酸化被膜が生成しているニツケ
ル薄膜層から前記酸化被膜を除去する方法におい
て、 前記電子部品のリードを有機酸液に浸漬する工
程と、その後前記電子部品のリードを過酸化水素
とフツ化アンモニウムを主成分とする化学研磨液
に浸漬する工程とを有することを特徴とするニツ
ケル酸化被膜除去方法。 2 特許請求の範囲第1項において、前記有機酸
液はほぼ沸点に加熱されたシユウ酸水溶液である
ニツケル酸化被膜除去方法。
[Scope of Claims] 1. A method for removing an oxide film from a nickel thin film layer that is attached to a lead led out from a package of an electronic component and has an oxide film formed on the surface, comprising: treating the lead of the electronic component with an organic acid. A method for removing a nickel oxide film, comprising the steps of immersing the electronic component in a liquid, and then immersing the lead of the electronic component in a chemical polishing liquid containing hydrogen peroxide and ammonium fluoride as main components. 2. The method for removing a nickel oxide film according to claim 1, wherein the organic acid solution is an oxalic acid aqueous solution heated to approximately the boiling point.
JP59076657A 1984-04-18 1984-04-18 Removing method of nickel oxide film Granted JPS60221585A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP59076657A JPS60221585A (en) 1984-04-18 1984-04-18 Removing method of nickel oxide film

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP59076657A JPS60221585A (en) 1984-04-18 1984-04-18 Removing method of nickel oxide film

Publications (2)

Publication Number Publication Date
JPS60221585A JPS60221585A (en) 1985-11-06
JPH0123554B2 true JPH0123554B2 (en) 1989-05-02

Family

ID=13611474

Family Applications (1)

Application Number Title Priority Date Filing Date
JP59076657A Granted JPS60221585A (en) 1984-04-18 1984-04-18 Removing method of nickel oxide film

Country Status (1)

Country Link
JP (1) JPS60221585A (en)

Families Citing this family (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JP4026573B2 (en) * 2003-09-24 2007-12-26 株式会社デンソー Method for manufacturing package for storing electronic device

Also Published As

Publication number Publication date
JPS60221585A (en) 1985-11-06

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