JPS60169589A - Copper alloy material containing phosphorus coated with tin or tin alloy - Google Patents

Copper alloy material containing phosphorus coated with tin or tin alloy

Info

Publication number
JPS60169589A
JPS60169589A JP2277784A JP2277784A JPS60169589A JP S60169589 A JPS60169589 A JP S60169589A JP 2277784 A JP2277784 A JP 2277784A JP 2277784 A JP2277784 A JP 2277784A JP S60169589 A JPS60169589 A JP S60169589A
Authority
JP
Japan
Prior art keywords
tin
alloy
plating
copper
layer
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.)
Pending
Application number
JP2277784A
Other languages
Japanese (ja)
Inventor
Toru Tanigawa
徹 谷川
Shoji Shiga
志賀 章二
Taku Kuroyanagi
黒柳 卓
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.)
Furukawa Electric Co Ltd
Original Assignee
Furukawa Electric 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 Furukawa Electric Co Ltd filed Critical Furukawa Electric Co Ltd
Priority to JP2277784A priority Critical patent/JPS60169589A/en
Publication of JPS60169589A publication Critical patent/JPS60169589A/en
Pending legal-status Critical Current

Links

Abstract

PURPOSE:To prevent the stripping of an Sn or Sn alloy coating formed on a Cu alloy substrate contg. P by forming a Zn or Zn alloy layer of a specified thickness as an intermediate layer on the substrate before forming the Sn or Sn alloy coating. CONSTITUTION:A Zn or Zn alloy layer of >=0.1mum, especially 0.1-3mum thickness as an intermediate layer is formed on a Cu alloy substrate contg. P. The preferred Zn alloy is Cu-Zn or Sn-Zn. An Sn or Sn alloy coating is then formed on the intermediate layer. The diffusion of P contained in the substrate into the Sn or Sn alloy coating is inhibited by the presence of the intermediate layer contg. Zn, so the stripping of the Sn or Sn alloy coating is prevented.

Description

【発明の詳細な説明】 〔技術分野〕 本発明は、リン青銅に代表されるリン含有鋼合金基材に
錫または錫合金被核層を設けてなる岐切材の改良に関す
るものである。
DETAILED DESCRIPTION OF THE INVENTION [Technical Field] The present invention relates to the improvement of a wood cutting material made by providing a tin or tin alloy nucleation layer on a phosphorus-containing steel alloy base material, typified by phosphor bronze.

〔従来技術〕[Prior art]

リン青銅は比較的良好な導電性と優れたバネ性、強度を
有することから、例えはコネクタや各種スイッチ、電磁
開閉器あるいはスフリングなど、各種電気・電子材料と
して広くオリ相場れている。またリンw銅は、良好な耐
食性を有するため、加工上りのまま使用されることもあ
るか、端子などに用いる場合には、半田付は性を向上さ
せる目的で、錫や錫合金(例えば半田)を被悔して使用
されることが多い。錫や錫合金の被覆は専ら電気メッキ
によることか多く、通常0.1〜1μ厚の銅を下地メッ
キとして、05〜3μの厚さにメッキされる。
Because phosphor bronze has relatively good conductivity, excellent springiness, and strength, it is widely used as a variety of electrical and electronic materials, such as connectors, various switches, electromagnetic switches, and spring rings. In addition, since phosphorous copper has good corrosion resistance, it is sometimes used as is after processing, or when used for terminals etc., it is soldered with tin or tin alloys (such as solder) to improve soldering properties. ) is often used with regret. Coating with tin or a tin alloy is often done exclusively by electroplating, and is usually plated to a thickness of 0.5 to 3 microns using a 0.1 to 1 micron thick copper as a base plating.

壕だ一部には、上記メッキ後、短時間加熱して、表面の
鐘や錫合金を浴融平滑化するりフロー処理が施されるこ
ともある。
After the above-mentioned plating, a part of the trench may be heated for a short time to smooth the bell or tin alloy on the surface by bath melting, or flow treatment may be applied.

銅と鵠または錫合金との接合時には、その界面に銅と我
とからなる2種の金属間化合物、すなわち錫B111に
η′相(Cu6Sns)と粗側にε相(CuaSn )
が形成されることが知られているが、基材の銅がリンを
含有しているときは、ε相のさらに銅(till K、
01〜0.2%のリンが井縮した相が形成される。
When bonding copper and copper or tin alloy, two types of intermetallic compounds consisting of copper and tin are formed at the interface, namely η' phase (Cu6Sns) on the tin B111 and ε phase (CuaSn) on the rough side.
is known to be formed, but when the copper base material contains phosphorus, further copper in the ε phase (till K,
A phase containing 0.01-0.2% phosphorus is formed.

この相は極めて脆く、長期間の使用で、錫捷たは轄r合
金被核屑が銅合金基材から剥離するという現象を生じさ
せる。また加熱条件下では短時間のうちに同様の現象が
生じる。このような現象が生じると、電気・電子機器の
回路障害ケ招き、依器の信頼性を著しく損う結果となる
This phase is extremely brittle, and after long-term use, a phenomenon occurs in which tin shavings or nucleated alloy chips peel off from the copper alloy base material. Moreover, under heating conditions, a similar phenomenon occurs within a short time. If such a phenomenon occurs, it may lead to circuit failures in electrical/electronic equipment, resulting in a significant loss of reliability of the equipment.

〔発明の目的〕[Purpose of the invention]

本発明の目的は、上記のような従来技術の問題点に!み
、錫または錫合金被0層の剥離を防止できる、リン含有
鋼合金の錫または錫合金被0層を提供することにある。
The purpose of the present invention is to solve the problems of the prior art as described above! It is an object of the present invention to provide a tin or tin alloy coating layer of a phosphorus-containing steel alloy that can prevent the tin or tin alloy coating layer from peeling.

〔発明の構成〕[Structure of the invention]

上記目的を達成する本発明のリン含有鋼台金の個または
錫合金被0層は、リン含有鋼台金基徊上に、厚さ01μ
以上好ましくは01〜:3μの!III鉛または亜鉛合
金中間層を介して、錫またはXit台釜被覆層を設けた
こと金付漱とするものである。
The phosphorus-containing steel base metal layer or tin alloy coating layer of the present invention that achieves the above object is coated on the phosphorus-containing steel base metal base with a thickness of 01 μm.
The above is preferably 01~:3μ! A tin or Xit pot coating layer is provided through a lead or zinc alloy intermediate layer.

亜鉛合金としては、Cu −ZnやSn −Znなとか
好適であるが、Ni−Zn 、 Ni−Co−Zn量 
Zn−Cd、I!”e−Znなどの合金を用いることも
できる 亜鉛またけ亜鉛合金中1ta1層の厚さは、Z
n量にもよるか、通常O1μ1μあれはよい。そ庇取下
では充分な剥離防止効果が得られない。また半田付は性
の面からはこの中間層の厚さは3μ以下が好ましい1、
亜鉛によるリン濃縮抑制のメカニズムは明らかではない
が、亜鉛含有中間層の存仕によf)Cu−8n金属間化
合物相の発達も同時に抑制されることから、銅合金基材
からのリンの拡散が亜鉛により抑制されることによるも
のと考えら扛る。
As the zinc alloy, Cu-Zn and Sn-Zn are suitable, but the amount of Ni-Zn, Ni-Co-Zn
Zn-Cd, I! ``Alloys such as e-Zn can also be used.
It depends on the amount of n, but normally O1μ1μ is good. If the eaves are removed, a sufficient peeling prevention effect cannot be obtained. In addition, from the viewpoint of soldering properties, it is preferable that the thickness of this intermediate layer is 3μ or less1.
Although the mechanism by which zinc inhibits phosphorus concentration is not clear, the presence of the zinc-containing intermediate layer also inhibits the development of the Cu-8n intermetallic compound phase, which suggests that phosphorus will diffuse from the copper alloy base material. It is thought that this is due to the fact that zinc suppresses this.

なお、本発明はリン宵銅のみならす他のリン含有鋼台金
を基材とする鵠または錫合金被0層にも〕釣用可能であ
る。
Note that the present invention can be applied not only to phosphorus-containing steel but also to other phosphorus-containing steel base metals or tin alloy coatings.

〔実施1911 ) 実jIm□り1」■ ノ早さ0.4mm、中425mmのリン宵附(Sn: 
7.9%。
[Implementation 1911] Real 1" ■ 0.4 mm in speed, 425 mm in diameter (Sn:
7.9%.

P:o、lz係)を暴利として、次の工程により釉々の
厚式の!II鉛メッキを中間層とする鏝メッキ(厚さ1
μ)被核材を作成した。なお、亜鉛メッキの八Jさは、
メッキ時liJを変えて調整し、0.05 、0.1 
P: o, lz section) as profiteers, the next step is to create a thick glaze! II Trowel plating with lead plating as the intermediate layer (thickness 1
μ) A nucleated material was created. In addition, the 8J size of galvanizing is
Adjust by changing liJ during plating, 0.05, 0.1
.

0.5,1.2.4μの6種とした。There were 6 types: 0.5, 1.2.4μ.

(1) カソード脱月j7 NaOH20g/f電流密
度 10A/dm’ 処理時間 10秒 (2) 水 (先 (3) 13り 洗 H2804100g/fH202
10g/l 安定剤 1−Og/Jl 処理時間 5秒 (4) 水 洗 (5)亜鉛メッキ ZnCN 60 g/fNaCN 
40 g/j! Na01−1 80 g/f 電流密度 IA/dm2 (6) 水 洗 (7) 光沢錫メッキ 5nS0440 g/fH2S
O4100g/、z ホルマリン 5cc/1 ′亀流智度 2.5 A/dm2 処理時間 50秒 (8) 水 洗 ゛(9) 乾 燥 実施例2 実施例1の亜鉛メッキに代え黄銅メッキ(Zn約30%
)を中間層とし、その他の条件ヲ四じにして、神々の被
核材を作成した。黄銅メッキの条件は次のとおシ。
(1) Cathode delunation j7 NaOH20g/f Current density 10A/dm' Processing time 10 seconds (2) Water (first (3) 13 ml Washing H2804100g/fH202
10g/l Stabilizer 1-Og/Jl Processing time 5 seconds (4) Water washing (5) Zinc plating ZnCN 60 g/fNaCN
40 g/j! Na01-1 80 g/f Current density IA/dm2 (6) Water washing (7) Bright tin plating 5nS0440 g/fH2S
O4 100g/, z Formalin 5cc/1 'Turtle flow rate 2.5 A/dm2 Processing time 50 seconds (8) Water Washing (9) Drying Example 2 Brass plating (Zn approx. 30%
) was used as the middle layer, and the other conditions were kept the same to create the nucleated material of the gods. The conditions for brass plating are as follows.

CuCN 30 g/J Z、、(CN)2 10 g/z NaCN 50 g/J4 Na、、Co3 :うOg/x 電流密度 I A、/dm2 浴 温 40C 実施例3 実施例1の亜鉛メッキに代えSo −Zn メッキ(Z
n 4′l 20 % ) f中1mj Ieとし7、
その他の条1午f 1TTiしにしで、神々の破ね、桐
を作成した。Sr+ −Znメッキの条件は次のとおり
CuCN 30 g/J Z,, (CN)2 10 g/z NaCN 50 g/J4 Na,, Co3: Og/x Current density I A,/dm2 Bath temperature 40C Example 3 For the zinc plating of Example 1 Alternative So-Zn plating (Z
n 4'l 20%) 1mj Ie in f7,
Other Articles 1 pm 1TTi I created Kiri, the destroyer of the gods. The conditions for Sr+ -Zn plating are as follows.

Na25n03・3f(4067g/lZ+1 (CN
)210 g/1 NaCN 25 g/、e NaOl−16g/f 電流否度 2 A/dm2 (谷 温 60r 従来例 実施例1の亜鉛メッキに代えり、さ1μの光沢銅メッキ
を中間JEとし、その他の条件を同じにして従来の被覆
材を作成した。光沢鉤メッキの条件は次のとおり。
Na25n03・3f (4067g/lZ+1 (CN
) 210 g/1 NaCN 25 g/, e NaOl-16 g/f Current rating 2 A/dm2 (Valley temperature 60 r Conventional example Instead of the zinc plating in Example 1, bright copper plating with a thickness of 1 μm was used as intermediate JE, A conventional coating material was prepared with other conditions being the same.The conditions for glossy hook plating were as follows.

Cu5O4a5H20220g/f 1(280455g/工 電流密度 3A/d+n2 以上のようにして作成さt′Lだ各錘の破mUにつき、
150C大気中で所定時間加熱後の折り曲けによる剥離
の元生状況と、230C共品半田に2秒浸漬したときの
藺れ面積による半田伺け1牛をル・勺べた。
Cu5O4a5H20220g/f 1 (280455g/working current density 3A/d+n2) For each weight mU created as above,
The origin of peeling due to bending after heating in 150C atmosphere for a predetermined period of time and the area of smearing when immersed in 230C solder for 2 seconds were investigated.

結果は次表のとおりである。The results are shown in the table below.

注)0)+徹1.[(ム7,1Nへ13は比蚊例である
Note) 0) + Toru 1. [(Mu7, 1N to 13 is a comparison example.

(2)剥離評価 ○:剥離なし ト]:僅かにわり △:部分的にあシ ×=剥 離 (3)半田付は性 ○:〉90% (濡れ面イ青) 口:8o〜90 % △:50〜80襲 X:(50% 〔発明の効果〕 以上説明したように本元明によれに2、銭またけ錫合金
被成層の剥離を実質的になくしたリン含有鋼合金の錫ま
たは錫合金被酸材を得ることかでき、電気・指、子機器
の信頼性向上に寄与するところ人である。
(2) Peeling evaluation ○: No peeling]: Slightly △: Partially peeled × = Peeling (3) Soldering is rough ○: >90% (Wet surface is blue) Mouth: 8o~90% △: 50 to 80 Alternatively, it is possible to obtain a tin alloy oxidizable material, which contributes to improving the reliability of electrical, electronic, and slave devices.

出頗人代理人 弁理士 若林広志にPatent attorney Hiroshi Wakabayashi is the agent

Claims (1)

【特許請求の範囲】[Claims] リン含有銅合金基村上に、厚さ01μ以上の亜鉛または
亜鉛合金中間/Gm ’に介して、錫または錫合金被核
層を設けたことを特徴とするリン含有鋼合金の錫または
錫合金被核層。
A tin or tin alloy coating of a phosphorus-containing steel alloy, characterized in that a tin or tin alloy nucleation layer is provided on a phosphorus-containing copper alloy base layer through a zinc or zinc alloy intermediate/Gm' having a thickness of 01μ or more. nuclear layer.
JP2277784A 1984-02-13 1984-02-13 Copper alloy material containing phosphorus coated with tin or tin alloy Pending JPS60169589A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP2277784A JPS60169589A (en) 1984-02-13 1984-02-13 Copper alloy material containing phosphorus coated with tin or tin alloy

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP2277784A JPS60169589A (en) 1984-02-13 1984-02-13 Copper alloy material containing phosphorus coated with tin or tin alloy

Publications (1)

Publication Number Publication Date
JPS60169589A true JPS60169589A (en) 1985-09-03

Family

ID=12092092

Family Applications (1)

Application Number Title Priority Date Filing Date
JP2277784A Pending JPS60169589A (en) 1984-02-13 1984-02-13 Copper alloy material containing phosphorus coated with tin or tin alloy

Country Status (1)

Country Link
JP (1) JPS60169589A (en)

Cited By (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US5759379A (en) * 1996-04-26 1998-06-02 International Business Machines Corporation Solder method
JP2018016878A (en) * 2016-07-29 2018-02-01 三菱マテリアル株式会社 Manufacturing method of tin plating copper terminal material

Citations (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS5641397A (en) * 1979-09-12 1981-04-18 Furukawa Electric Co Ltd:The Copper-group material excellent in resistance to corrosion

Patent Citations (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS5641397A (en) * 1979-09-12 1981-04-18 Furukawa Electric Co Ltd:The Copper-group material excellent in resistance to corrosion

Cited By (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US5759379A (en) * 1996-04-26 1998-06-02 International Business Machines Corporation Solder method
JP2018016878A (en) * 2016-07-29 2018-02-01 三菱マテリアル株式会社 Manufacturing method of tin plating copper terminal material

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