JPH0210237B2 - - Google Patents
Info
- Publication number
- JPH0210237B2 JPH0210237B2 JP12757282A JP12757282A JPH0210237B2 JP H0210237 B2 JPH0210237 B2 JP H0210237B2 JP 12757282 A JP12757282 A JP 12757282A JP 12757282 A JP12757282 A JP 12757282A JP H0210237 B2 JPH0210237 B2 JP H0210237B2
- Authority
- JP
- Japan
- Prior art keywords
- plating
- strike
- electrolytic
- gold
- potassium
- 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
Links
- XEEYBQQBJWHFJM-UHFFFAOYSA-N Iron Chemical compound [Fe] XEEYBQQBJWHFJM-UHFFFAOYSA-N 0.000 claims description 18
- 239000003795 chemical substances by application Substances 0.000 claims description 13
- 229910000990 Ni alloy Inorganic materials 0.000 claims description 9
- PXHVJJICTQNCMI-UHFFFAOYSA-N Nickel Chemical compound [Ni] PXHVJJICTQNCMI-UHFFFAOYSA-N 0.000 claims description 7
- 229910000640 Fe alloy Inorganic materials 0.000 claims description 6
- 239000012190 activator Substances 0.000 claims description 6
- PCHJSUWPFVWCPO-UHFFFAOYSA-N gold Chemical compound [Au] PCHJSUWPFVWCPO-UHFFFAOYSA-N 0.000 claims description 6
- 229910052737 gold Inorganic materials 0.000 claims description 6
- 239000010931 gold Substances 0.000 claims description 6
- 150000003839 salts Chemical class 0.000 claims description 6
- 229910052751 metal Inorganic materials 0.000 claims description 5
- 239000002184 metal Substances 0.000 claims description 5
- 229910052759 nickel Inorganic materials 0.000 claims description 4
- NRTDAKURTMLAFN-UHFFFAOYSA-N potassium;gold(3+);tetracyanide Chemical compound [K+].[Au+3].N#[C-].N#[C-].N#[C-].N#[C-] NRTDAKURTMLAFN-UHFFFAOYSA-N 0.000 claims description 3
- 229910017052 cobalt Inorganic materials 0.000 claims description 2
- 239000010941 cobalt Substances 0.000 claims description 2
- GUTLYIVDDKVIGB-UHFFFAOYSA-N cobalt atom Chemical compound [Co] GUTLYIVDDKVIGB-UHFFFAOYSA-N 0.000 claims description 2
- 150000004696 coordination complex Chemical group 0.000 claims 1
- 238000007747 plating Methods 0.000 description 24
- 229910052709 silver Inorganic materials 0.000 description 9
- 239000004332 silver Substances 0.000 description 9
- BQCADISMDOOEFD-UHFFFAOYSA-N Silver Chemical compound [Ag] BQCADISMDOOEFD-UHFFFAOYSA-N 0.000 description 7
- 238000000034 method Methods 0.000 description 7
- RYGMFSIKBFXOCR-UHFFFAOYSA-N Copper Chemical compound [Cu] RYGMFSIKBFXOCR-UHFFFAOYSA-N 0.000 description 6
- 229910052802 copper Inorganic materials 0.000 description 6
- 239000010949 copper Substances 0.000 description 6
- 238000011282 treatment Methods 0.000 description 6
- MUBZPKHOEPUJKR-UHFFFAOYSA-N Oxalic acid Chemical compound OC(=O)C(O)=O MUBZPKHOEPUJKR-UHFFFAOYSA-N 0.000 description 3
- KRKNYBCHXYNGOX-UHFFFAOYSA-N citric acid Chemical compound OC(=O)CC(O)(C(O)=O)CC(O)=O KRKNYBCHXYNGOX-UHFFFAOYSA-N 0.000 description 3
- 238000005238 degreasing Methods 0.000 description 3
- XTFKWYDMKGAZKK-UHFFFAOYSA-N potassium;gold(1+);dicyanide Chemical compound [K+].[Au+].N#[C-].N#[C-] XTFKWYDMKGAZKK-UHFFFAOYSA-N 0.000 description 3
- 238000002203 pretreatment Methods 0.000 description 3
- 230000004913 activation Effects 0.000 description 2
- 238000002845 discoloration Methods 0.000 description 2
- 229910052742 iron Inorganic materials 0.000 description 2
- 229910000833 kovar Inorganic materials 0.000 description 2
- WABPQHHGFIMREM-UHFFFAOYSA-N lead(0) Chemical compound [Pb] WABPQHHGFIMREM-UHFFFAOYSA-N 0.000 description 2
- 239000007788 liquid Substances 0.000 description 2
- 239000000203 mixture Substances 0.000 description 2
- LNOPIUAQISRISI-UHFFFAOYSA-N n'-hydroxy-2-propan-2-ylsulfonylethanimidamide Chemical compound CC(C)S(=O)(=O)CC(N)=NO LNOPIUAQISRISI-UHFFFAOYSA-N 0.000 description 2
- BWHMMNNQKKPAPP-UHFFFAOYSA-L potassium carbonate Chemical compound [K+].[K+].[O-]C([O-])=O BWHMMNNQKKPAPP-UHFFFAOYSA-L 0.000 description 2
- NNFCIKHAZHQZJG-UHFFFAOYSA-N potassium cyanide Chemical compound [K+].N#[C-] NNFCIKHAZHQZJG-UHFFFAOYSA-N 0.000 description 2
- LWIHDJKSTIGBAC-UHFFFAOYSA-K tripotassium phosphate Chemical compound [K+].[K+].[K+].[O-]P([O-])([O-])=O LWIHDJKSTIGBAC-UHFFFAOYSA-K 0.000 description 2
- 229920000298 Cellophane Polymers 0.000 description 1
- FEWJPZIEWOKRBE-JCYAYHJZSA-N Dextrotartaric acid Chemical compound OC(=O)[C@H](O)[C@@H](O)C(O)=O FEWJPZIEWOKRBE-JCYAYHJZSA-N 0.000 description 1
- FEWJPZIEWOKRBE-UHFFFAOYSA-N Tartaric acid Natural products [H+].[H+].[O-]C(=O)C(O)C(O)C([O-])=O FEWJPZIEWOKRBE-UHFFFAOYSA-N 0.000 description 1
- UCFIGPFUCRUDII-UHFFFAOYSA-N [Co](C#N)C#N.[K] Chemical compound [Co](C#N)C#N.[K] UCFIGPFUCRUDII-UHFFFAOYSA-N 0.000 description 1
- YLZGVPCTROQQSX-UHFFFAOYSA-N [K].[Ni](C#N)C#N Chemical compound [K].[Ni](C#N)C#N YLZGVPCTROQQSX-UHFFFAOYSA-N 0.000 description 1
- 239000002253 acid Substances 0.000 description 1
- 230000002378 acidificating effect Effects 0.000 description 1
- 230000003213 activating effect Effects 0.000 description 1
- 239000003513 alkali Substances 0.000 description 1
- 229910045601 alloy Inorganic materials 0.000 description 1
- 239000000956 alloy Substances 0.000 description 1
- 239000002585 base Substances 0.000 description 1
- 238000005452 bending Methods 0.000 description 1
- KXZJHVJKXJLBKO-UHFFFAOYSA-N chembl1408157 Chemical compound N=1C2=CC=CC=C2C(C(=O)O)=CC=1C1=CC=C(O)C=C1 KXZJHVJKXJLBKO-UHFFFAOYSA-N 0.000 description 1
- 235000015165 citric acid Nutrition 0.000 description 1
- 238000005260 corrosion Methods 0.000 description 1
- 230000007797 corrosion Effects 0.000 description 1
- 238000009792 diffusion process Methods 0.000 description 1
- 230000000694 effects Effects 0.000 description 1
- 239000000463 material Substances 0.000 description 1
- 150000007524 organic acids Chemical class 0.000 description 1
- 235000006408 oxalic acid Nutrition 0.000 description 1
- 229910000027 potassium carbonate Inorganic materials 0.000 description 1
- 239000001508 potassium citrate Substances 0.000 description 1
- 229960002635 potassium citrate Drugs 0.000 description 1
- QEEAPRPFLLJWCF-UHFFFAOYSA-K potassium citrate (anhydrous) Chemical compound [K+].[K+].[K+].[O-]C(=O)CC(O)(CC([O-])=O)C([O-])=O QEEAPRPFLLJWCF-UHFFFAOYSA-K 0.000 description 1
- 235000011082 potassium citrates Nutrition 0.000 description 1
- 229910000160 potassium phosphate Inorganic materials 0.000 description 1
- 235000011009 potassium phosphates Nutrition 0.000 description 1
- 239000002244 precipitate Substances 0.000 description 1
- 230000009467 reduction Effects 0.000 description 1
- 239000004065 semiconductor Substances 0.000 description 1
- 239000010935 stainless steel Substances 0.000 description 1
- 229910001220 stainless steel Inorganic materials 0.000 description 1
- -1 stainless steel) Chemical compound 0.000 description 1
- 239000000758 substrate Substances 0.000 description 1
- 239000011975 tartaric acid Substances 0.000 description 1
- 235000002906 tartaric acid Nutrition 0.000 description 1
Landscapes
- Electroplating Methods And Accessories (AREA)
Description
【発明の詳細な説明】
本発明は鉄、ニツケル合金のメツキ処理に好適
な電解前処理剤に関する。DETAILED DESCRIPTION OF THE INVENTION The present invention relates to an electrolytic pretreatment agent suitable for plating iron and nickel alloys.
鉄(例えばステンレスステイール)、ニツケル
合金(例えばNi42%、Fe残部の「42アロイ」、
Ni29%、コバール17%、Fe残部の「コバール」
等)をメツキする場合、従来は本メツキ前にスト
ライクメツキすることが不可欠であるとされてい
る。これは素地に対するメツキ(例えば銀メツ
キ)の密着性が悪いのでこれを予め向上させるた
めのものであり、従来は一般的に脱脂、活性、ス
トライク、の各処理を施して後に本メツキし更に
必要に応じ不要なストライクメツキを剥離する等
の工程を経て鉄、ニツケル合金のメツキ処理を行
なつている。 Iron (e.g. stainless steel), nickel alloy (e.g. 42% Ni alloy with the remainder Fe,
"Kovar" with 29% Ni, 17% Kovar, and the balance of Fe
etc.), it has conventionally been considered essential to perform strike plating before main plating. This is to improve the adhesion of plating (for example, silver plating) to the base material beforehand, and conventionally, it has been common practice to perform degreasing, activation, and strike treatments, and then apply the final plating. Plating of iron and nickel alloys is performed through processes such as peeling off unnecessary strike plating.
しかしながら、ストライクメツキ処理は本メツ
キ処理同様に慎重な扱いが要求され、高価でもあ
り(例えば金ストライク、銀ストライクの場合)、
剥離工程が必要なので(例えば銅ストライク−銀
本メツキの場合の銅ストライクの剥離)、これを
省略できれば各種のメツキ処理に於いて多くの利
点がある。 However, the strike plating process, like the main plating process, requires careful handling and is expensive (for example, in the case of gold strikes and silver strikes).
Since a stripping step is required (for example, stripping the copper strike in the case of copper strike-silver plating), there are many advantages in various plating processes if this can be omitted.
本発明はこの点に注目して従来のメツキ処理に
不可欠なストライク処理、ストライク工程を省略
できるような電解前処理剤を提供せんとするもの
である。そして具体的には、本発明に係る鉄、ニ
ツケル合金の電解前処理剤は各種電導塩と、アノ
ード活性剤と、シアン化金カリウムを含有してい
るものである。 The present invention focuses on this point and aims to provide an electrolytic pretreatment agent that can omit the strike treatment and strike step that are essential to conventional plating treatment. Specifically, the electrolytic pretreatment agent for iron and nickel alloys according to the present invention contains various conductive salts, an anode activator, and potassium gold cyanide.
先ずこの電解前処理剤は各種電導塩として以下
のものを選択的に含有する。 First, this electrolytic pretreatment agent selectively contains the following as various conductive salts.
シアン化カリウム 5〜150g/
シアン化ナトリウム 10〜250g/
有機酸(例えばクエン酸、修酸、酒石酸等の塩
類) 20〜200g/
スルフアミン酸(例えばスルフアミン酸及び塩
類) 10〜250g/
次にこの電解前処理剤はアノード活性剤を含有
する。このアノード活性剤としては、例えばニツ
ケル、コバルト等の金属錯体が好適であり、0.5
〜50g/程度含有せしめるものである。 Potassium cyanide 5-150g / Sodium cyanide 10-250g / Organic acid (e.g. salts such as citric acid, oxalic acid, tartaric acid, etc.) 20-200g / Sulfamic acid (e.g. sulfamic acid and salts) 10-250g / Next, this electrolytic pretreatment The agent contains an anode activator. As this anode activator, metal complexes such as nickel and cobalt are suitable, and 0.5
~50g/approximately.
更に電解前処理剤はシアン化金カリウムを含有
する。含有量は微量でよく、例えば金メタルとし
て5〜200ppm0.05〜2g/)程度でよい。 Further, the electrolytic pretreatment agent contains gold potassium cyanide. The content may be a trace amount, for example, about 5 to 200 ppm (0.05 to 2 g/) as gold metal.
このような電解前処理剤で鉄、ニツケル合金を
脱脂、活性、に続いて前処理するには電解前処理
剤を用いた液(以下「電解前処理剤」と称す)
を、以下の条件で操作するものである。 To pre-treat iron and nickel alloys after degreasing and activating them with such an electrolytic pre-treatment agent, a solution using an electrolytic pre-treatment agent (hereinafter referred to as "electrolytic pre-treatment agent") is required.
is operated under the following conditions.
PH 3.0以上 電圧 1〜8V 時間 5〜120秒 温度 室温〜70℃ 次に実施例を説明する。PH 3.0 or higher Voltage 1~8V Time 5-120 seconds Temperature Room temperature ~ 70℃ Next, an example will be described.
実施例 1
電解前処理液組成
シアン化カリウム 50g/
炭酸カリウム 20g/
シアン化ニツケルカリウム 10g/
シアン化金カリウム
0.1g/(金メタルとして)
操作条件
電圧 6V
時間 20sec
温度 35℃
以上の条件でコバール材ICリードフレームを
脱脂、活性に続いて電解前処理し、ストライクメ
ツキすることなく、直接銀メツキを3μ施した。
そしてセロハンテープ(商品名)にて剥離テスト
を行なつたが銀メツキの剥離はなく密着性の向上
していることが確認できた。更に380℃、5分間
の耐熱テストを加えたが変色やふくれは見当らな
かつた。Example 1 Electrolytic pretreatment liquid composition Potassium cyanide 50g / Potassium carbonate 20g / Potassium nickel cyanide 10g / Potassium gold cyanide
0.1g/(as gold metal) Operating conditions Voltage 6V Time 20sec Temperature 35°C or above, the Kovar IC lead frame is degreased and activated, followed by electrolytic pretreatment, and directly silver plated to 3μ without strike plating. did.
A peel test was then performed using cellophane tape (trade name), but the silver plating did not peel off, confirming that the adhesion had improved. We also conducted a heat resistance test at 380℃ for 5 minutes, but no discoloration or blistering was found.
実施例 2
前処理液組成
クエン酸カリウム 100g/
リン酸カリウム 10g/
シアン化コバルトカリウム 10g/
シアン化金カリウム
0.2g/(金メタルとして)
操作条件
PH 6.8
電圧 4V
時間 20sec
温度 60℃
以上の条件で42アロイ材の半導体のリード線を
脱脂、活性に続いて電解前処理し、ストライクメ
ツキすることなく、直接銀メツキを3μ施した。
このリード線を折り曲げテストにかけたが、銀メ
ツキの剥離は全く見られず、更に380℃、5分間
の耐熱テストを加えたが変色もふくれも発生しな
かつた。Example 2 Pretreatment liquid composition Potassium citrate 100g/ Potassium phosphate 10g/ Potassium cobalt cyanide 10g/ Potassium gold cyanide
0.2g/(as gold metal) Operating conditions PH 6.8 Voltage 4V Time 20sec Temperature 60°C or above, the lead wire of the 42 alloy semiconductor is degreased and activated, followed by electrolytic pretreatment, and directly applied without strike plating. 3μ silver plating was applied.
When this lead wire was subjected to a bending test, no peeling of the silver plating was observed, and a heat resistance test at 380°C for 5 minutes was also performed, but no discoloration or blistering occurred.
以上説明してきたように、本発明によれば各種
電導塩にアノード活性剤を組合わせ且つ微量のシ
アン化金カリウムを用いることとしたため、鉄、
ニツケル合金の素地にニツケルストライク、金ス
トライク、銀ストライク、銅ストライク等のスト
ライクメツキ処理を施すことなく脱脂、活性に続
いてこの電解前処理剤を用いた電解前処理を行な
うのみで直接本メツキすることが可能となり、従
来ストライクの不可欠であつたメツキ処理に対し
その分処理が簡便化されコストダウンに寄与で
き、それでいて従来同等の密着性の向上が期待で
きる上に、強酸ではなく弱酸性アルカリ処理なの
で耐食性の向上があり、しかも銅ストライク−銀
メツキの如き従来のメツキ処理の場合析出物の表
面に銅がいわば拡散現象で出て来て酸化物を生成
し易いという不具合が見受けられたが本発明の前
処理剤を使用すれば銅ストライクを不要とするた
めこのような不具合を完全に解消し電気的特性の
向上に寄与できるという効果もある。更には剥離
処理も省略可能なのでその分経済的でもあり従来
のメツキ処理に比べて多くの利点がある。 As explained above, according to the present invention, since various conductive salts are combined with an anode activator and a trace amount of gold potassium cyanide is used, iron,
Direct plating is performed on the nickel alloy substrate by simply performing electrolytic pretreatment using this electrolytic pretreatment agent following degreasing and activation without performing strike plating treatment such as nickel strike, gold strike, silver strike, or copper strike. This simplifies the plating process, which was indispensable for conventional strikes, and contributes to cost reductions.It can also be expected to improve adhesion to the same level as conventional strikes, and requires weakly acidic alkali treatment instead of strong acid. Therefore, corrosion resistance is improved, and in addition, in conventional plating treatments such as copper strike-silver plating, copper comes out on the surface of precipitates by a so-called diffusion phenomenon and tends to generate oxides. Use of the pretreatment agent of the invention eliminates the need for copper strikes, which has the effect of completely eliminating such problems and contributing to improved electrical characteristics. Furthermore, since the peeling process can be omitted, it is also economical and has many advantages over conventional plating processes.
Claims (1)
剤を0.5〜50g/及びシアン化金カリウムを金メ
タルとして0.05〜2g/含有して成る鉄、ニツケ
ル合金の電解前処理剤。 2 アノード活性剤がニツケル、コバルトの金属
錯体である特許請求の範囲第1項記載の鉄、ニツ
ケル合金の電解前処理剤。[Claims] 1. An electrolytic pretreatment agent for iron and nickel alloys containing 5 to 250 g of various conductive salts, 0.5 to 50 g of an anode activator, and 0.05 to 2 g of gold potassium cyanide as gold metal. . 2. The electrolytic pretreatment agent for iron and nickel alloys according to claim 1, wherein the anode activator is a metal complex of nickel and cobalt.
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP12757282A JPS5920493A (en) | 1982-07-23 | 1982-07-23 | Pretreating agent for iron-nickel alloy |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP12757282A JPS5920493A (en) | 1982-07-23 | 1982-07-23 | Pretreating agent for iron-nickel alloy |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| JPS5920493A JPS5920493A (en) | 1984-02-02 |
| JPH0210237B2 true JPH0210237B2 (en) | 1990-03-07 |
Family
ID=14963357
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP12757282A Granted JPS5920493A (en) | 1982-07-23 | 1982-07-23 | Pretreating agent for iron-nickel alloy |
Country Status (1)
| Country | Link |
|---|---|
| JP (1) | JPS5920493A (en) |
-
1982
- 1982-07-23 JP JP12757282A patent/JPS5920493A/en active Granted
Also Published As
| Publication number | Publication date |
|---|---|
| JPS5920493A (en) | 1984-02-02 |
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