JPH0467726B2 - - Google Patents
Info
- Publication number
- JPH0467726B2 JPH0467726B2 JP18357987A JP18357987A JPH0467726B2 JP H0467726 B2 JPH0467726 B2 JP H0467726B2 JP 18357987 A JP18357987 A JP 18357987A JP 18357987 A JP18357987 A JP 18357987A JP H0467726 B2 JPH0467726 B2 JP H0467726B2
- Authority
- JP
- Japan
- Prior art keywords
- tin
- copper
- alloy
- plating
- contact
- 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
- ATJFFYVFTNAWJD-UHFFFAOYSA-N Tin Chemical compound [Sn] ATJFFYVFTNAWJD-UHFFFAOYSA-N 0.000 claims description 22
- 238000007747 plating Methods 0.000 claims description 22
- 229910001174 tin-lead alloy Inorganic materials 0.000 claims description 18
- RYGMFSIKBFXOCR-UHFFFAOYSA-N Copper Chemical compound [Cu] RYGMFSIKBFXOCR-UHFFFAOYSA-N 0.000 claims description 14
- 239000010949 copper Substances 0.000 claims description 14
- 229910052802 copper Inorganic materials 0.000 claims description 13
- 229910000881 Cu alloy Inorganic materials 0.000 claims description 12
- 238000010438 heat treatment Methods 0.000 claims description 8
- 239000000463 material Substances 0.000 claims description 8
- 238000002844 melting Methods 0.000 claims description 8
- 230000008018 melting Effects 0.000 claims description 8
- KUNSUQLRTQLHQQ-UHFFFAOYSA-N copper tin Chemical compound [Cu].[Sn] KUNSUQLRTQLHQQ-UHFFFAOYSA-N 0.000 claims description 7
- 238000000034 method Methods 0.000 claims description 7
- 238000009736 wetting Methods 0.000 claims description 7
- 229910045601 alloy Inorganic materials 0.000 claims description 6
- 239000000956 alloy Substances 0.000 claims description 6
- 238000004519 manufacturing process Methods 0.000 claims description 6
- OAICVXFJPJFONN-UHFFFAOYSA-N Phosphorus Chemical compound [P] OAICVXFJPJFONN-UHFFFAOYSA-N 0.000 claims description 5
- 229910000906 Bronze Inorganic materials 0.000 claims description 4
- 239000010974 bronze Substances 0.000 claims description 4
- 238000009713 electroplating Methods 0.000 claims description 4
- 238000009792 diffusion process Methods 0.000 claims description 2
- 229910001128 Sn alloy Inorganic materials 0.000 description 11
- 230000000694 effects Effects 0.000 description 5
- 239000000203 mixture Substances 0.000 description 5
- QAOWNCQODCNURD-UHFFFAOYSA-N Sulfuric acid Chemical compound OS(O)(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-N 0.000 description 4
- 239000002131 composite material Substances 0.000 description 4
- 238000005260 corrosion Methods 0.000 description 3
- 230000007797 corrosion Effects 0.000 description 3
- PCHJSUWPFVWCPO-UHFFFAOYSA-N gold Chemical compound [Au] PCHJSUWPFVWCPO-UHFFFAOYSA-N 0.000 description 3
- 229910052737 gold Inorganic materials 0.000 description 3
- 239000010931 gold Substances 0.000 description 3
- BQCADISMDOOEFD-UHFFFAOYSA-N Silver Chemical compound [Ag] BQCADISMDOOEFD-UHFFFAOYSA-N 0.000 description 2
- 239000000654 additive Substances 0.000 description 2
- 230000000996 additive effect Effects 0.000 description 2
- 238000005238 degreasing Methods 0.000 description 2
- 229910052751 metal Inorganic materials 0.000 description 2
- 239000002184 metal Substances 0.000 description 2
- 239000010956 nickel silver Substances 0.000 description 2
- 229910052703 rhodium Inorganic materials 0.000 description 2
- 239000010948 rhodium Substances 0.000 description 2
- MHOVAHRLVXNVSD-UHFFFAOYSA-N rhodium atom Chemical compound [Rh] MHOVAHRLVXNVSD-UHFFFAOYSA-N 0.000 description 2
- 229910052709 silver Inorganic materials 0.000 description 2
- 239000004332 silver Substances 0.000 description 2
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 2
- 229910001369 Brass Inorganic materials 0.000 description 1
- 229910017482 Cu 6 Sn 5 Inorganic materials 0.000 description 1
- 229910000978 Pb alloy Inorganic materials 0.000 description 1
- QAOWNCQODCNURD-UHFFFAOYSA-L Sulfate Chemical compound [O-]S([O-])(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-L 0.000 description 1
- 239000002253 acid Substances 0.000 description 1
- 239000010953 base metal Substances 0.000 description 1
- DMFGNRRURHSENX-UHFFFAOYSA-N beryllium copper Chemical compound [Be].[Cu] DMFGNRRURHSENX-UHFFFAOYSA-N 0.000 description 1
- 239000010951 brass Substances 0.000 description 1
- 239000001273 butane Substances 0.000 description 1
- 230000000052 comparative effect Effects 0.000 description 1
- 229910000365 copper sulfate Inorganic materials 0.000 description 1
- IUYOGGFTLHZHEG-UHFFFAOYSA-N copper titanium Chemical compound [Ti].[Cu] IUYOGGFTLHZHEG-UHFFFAOYSA-N 0.000 description 1
- ARUVKPQLZAKDPS-UHFFFAOYSA-L copper(II) sulfate Chemical compound [Cu+2].[O-][S+2]([O-])([O-])[O-] ARUVKPQLZAKDPS-UHFFFAOYSA-L 0.000 description 1
- 230000002950 deficient Effects 0.000 description 1
- 239000000295 fuel oil Substances 0.000 description 1
- 238000005461 lubrication Methods 0.000 description 1
- 239000011159 matrix material Substances 0.000 description 1
- 238000000691 measurement method Methods 0.000 description 1
- 238000010309 melting process Methods 0.000 description 1
- IJDNQMDRQITEOD-UHFFFAOYSA-N n-butane Chemical compound CCCC IJDNQMDRQITEOD-UHFFFAOYSA-N 0.000 description 1
- OFBQJSOFQDEBGM-UHFFFAOYSA-N n-pentane Natural products CCCCC OFBQJSOFQDEBGM-UHFFFAOYSA-N 0.000 description 1
- 238000006386 neutralization reaction Methods 0.000 description 1
- MOFOBJHOKRNACT-UHFFFAOYSA-N nickel silver Chemical compound [Ni].[Ag] MOFOBJHOKRNACT-UHFFFAOYSA-N 0.000 description 1
- 229910000510 noble metal Inorganic materials 0.000 description 1
- 229910052698 phosphorus Inorganic materials 0.000 description 1
- 239000011574 phosphorus Substances 0.000 description 1
- 238000005554 pickling Methods 0.000 description 1
- BASFCYQUMIYNBI-UHFFFAOYSA-N platinum Chemical group [Pt] BASFCYQUMIYNBI-UHFFFAOYSA-N 0.000 description 1
- 230000001846 repelling effect Effects 0.000 description 1
- 229910000679 solder Inorganic materials 0.000 description 1
- 239000000758 substrate Substances 0.000 description 1
- 239000010409 thin film Substances 0.000 description 1
Landscapes
- Electroplating Methods And Accessories (AREA)
- Manufacture Of Switches (AREA)
- Contacts (AREA)
Description
[産業上の利用分野]
本発明は電気的接続性に優れた接触子の製造方
法に関し、特には低い接圧力においても、接触抵
抗が低く、安定している接触子を製造せんとする
ものである。
[従来の技術]
銅又は銅合金に接点用金属として錫又は錫−鉛
合金を電気めつき後、加熱溶融処理を施した複合
材は民生用電子機器の接触子として多用されてい
る。
一方、接触信頼性が高度に要求される機器、部
品における接触子の接点用金属としては、金、
銀、ロジウム等が使用される。
[発明が解決しようとする問題点]
銅又は銅合金に錫又は錫−鉛合金をめつきした
複合材は、錫又は錫−鉛合金は貴金属に比べ耐食
性が低く、各種の腐蝕環境での腐蝕生成物や微摺
動摩耗腐蝕などにより低い接圧力では接触抵抗が
安定し難い問題があり、又、金、銀、ロジウム等
は低い接圧力で接触抵抗が低く安定しているもの
の高価である問題がある。
[問題点を解決するための手段]
本発明は、上記問題点を解決するためになされ
たもので、銅又は銅合金に錫又は錫−鉛合金をめ
つきした複合材であつて、しかも低い接圧力で接
触抵抗が低く安定している接触子を提供せんとす
るもので、銅又は銅合金に錫又は錫−鉛合金を電
気めつきした後、該めつき層を加熱溶融する方法
において、加熱溶融時に溶融錫又は溶融錫−鉛合
金のぬれ不良現象によるめつき厚みのばらつきの
程度すなわちめつき層厚みの最大値と最小値の差
が1cm2当り0.07〜0.3μmとすることを特徴とする
接触子の製造方法である。
銅合金としては、りん青銅、黄銅、洋白、ベリ
リウム銅、チタン銅等多種の銅合金が用いられる
が、本発明はこれらの銅合金に直接或いは銅下地
めつきを行つた後、錫或いは錫−鉛合金を電気め
つきする。
次にこれを錫あるいは錫−鉛合金の融点以上の
温度に保持し、銅−錫合金層の厚みおよびぬれ不
良の程度が所望の状態になつたところで水冷す
る。
銅下地めつき、錫めつき及び錫−鉛合金めつき
の条件は公知のことであり、これらの中から適宜
選択して実施することができる。
錫−鉛合金めつきは一般に半田めつきと呼ばれ
るもので、錫90wt%−鉛10wt%又は錫60wt%−
鉛40wt%の組成のものが最も多く用いられる。
加熱溶融処理には重油、ブタン等の直火型の炉
の他、電気炉、赤外線炉、高周波加熱炉等いずれ
を用いても良く、これらにより本発明は制限され
ない。
銅又は銅合金上の錫又は錫−鉛合金層を加熱溶
融すると、これに付随する一つの現象として“ぬ
れ不良”がある。これは“dewetting”、“はじ
き”などとも呼ばれ、溶融状態の錫又は錫−鉛合
金が母材又は下地とのぬれ不良により凝集し、小
滴になろうとして生じるものである。ぬれ不良は
外観、半田付性等の品質面から好ましくないた
め、従来その発生を押える数々の試みがなされて
いる。
しかしながら、本発明では接触性の面からは、
ぬれ不良によるめつき厚みの不均一がむしろ好ま
しいことを見出した。その範囲は1cm2当り0.07〜
0.3μmが適当である。0.07μm以下では効果が低
く、0.3μm以上では外観が著しく低下し好ましく
ない。
めつき厚みの不均一が上記範囲の場合、接触子
の接触部において境界抵抗および集中抵抗を低減
する作用が生じるものと考えられる。
銅又は銅合金上の錫又は錫−鉛合金層を加熱溶
融すると、母材又は下地の銅とめつき層中の錫と
の拡散生成物としてCu6Sn5相とCu3Sn相およびそ
の他の母材元素を含む銅−錫合金層が形成され
る。通常めつき層が溶融した直後に水冷凝固させ
ても、0.1〜0.3μm程度の厚みの合金層が生じる
が、これを溶融状態で数秒ないし10秒以上保持す
ると、合金層の厚みが0.4〜1.2μmとなる。
これら形成された合金層のビツカース硬度は
350〜450にもなり、その上層に残留する錫又は錫
−鉛合金層の50以下に比べ著しく硬い。したがつ
て、両層により薄膜金属潤滑作用が発生し、電気
接点とし接圧をかけ接触させた時、摺動あるいは
嵌合が滑らかで、かつ接触抵抗も低いものと考え
られる。
合金層の厚みが0.4μm未満ではそのような効果
が認められない。又、1.2μmを越える場合、接触
抵抗は良好であるが、外観が低下する傾向が認め
られるため接触子用素材として好ましくない。
銅下地めつきを省略し、銅合金母材に直接施し
た錫又は錫−鉛合金めつきは、めつき前処理によ
り、ぬれ不良の状況を調整できるため好適であ
る。
さらに母材がりん青銅(錫1〜8wt%、りん
0.03〜0.35wt%)の場合、合金層の成長が速やか
であり、接触子として用いた場合、従来品に比べ
接触抵抗が低く安定している。
[実施例]
銅、洋白およびりん青銅の0.2mm厚の板をアル
カリ脱脂、電解脱脂及び酸洗中和後、電気めつき
を施した。各種めつき条件は下記の通りである。
銅めつき
浴組成:硫酸銅 240g/
硫 酸 80g/
浴 温:30℃
電流密度:5A/dm2
錫めつき
浴組成:硫酸第1錫 60g/
硫 酸 70g/
添加剤 15g/
浴 温:20℃
電流密度:2A/dm2
半田(錫鉛合金)めつき
浴組成:ホウフツ化鉛 54g/
ホウフツ化錫 130g/
ホウフツ酸 90g/
添加材 30g/
浴 温:20℃
電流密度:5A/dm2
電気めつき後の加熱溶融処理は、電気炉中600
℃の雰囲気温度に数秒ないし数10秒保持し、銅−
錫合金層を形成させた後、水冷、温風乾燥した。
銅−錫合金層の厚みは、電解式厚み測定法により
行つた。
接触抵抗は試料面上で50gの荷重を負荷した半
径5mmの白金リングを10mm/minの速度で5mmの
距離を移動、往復させ、10mAの直流電流を流
し、接触抵抗を測定した。往復回数は500回とし
た。移動、往復に伴い接触抵抗は変動するため範
囲で示す。また、その時試料にひずみゲージを接
触させ、摩擦抵抗を測定し、相対的に大小で表わ
した。
結果を第1表に示す。第1表の結果から明らか
なように実施例は比較例に比べ接触抵抗が低く、
かつ変動も少ない。さらに摩擦抵抗も低いため、
接触子用組成として好適である。
[Industrial Application Field] The present invention relates to a method for manufacturing a contact with excellent electrical connectivity, and in particular, it is aimed at manufacturing a contact that has low contact resistance and is stable even under low contact pressure. be. [Prior Art] Composite materials obtained by electroplating copper or copper alloy with tin or tin-lead alloy as a contact metal and then subjecting the composite to heating and melting treatment are often used as contacts in consumer electronic devices. On the other hand, gold, gold,
Silver, rhodium, etc. are used. [Problems to be solved by the invention] Composite materials in which copper or copper alloys are plated with tin or tin-lead alloys are susceptible to corrosion in various corrosive environments because tin or tin-lead alloys have lower corrosion resistance than noble metals. There is a problem that the contact resistance is difficult to stabilize at low contact pressure due to products and micro-sliding wear and corrosion.Also, gold, silver, rhodium, etc. have low and stable contact resistance at low contact pressure, but are expensive. There is. [Means for Solving the Problems] The present invention was made to solve the above problems, and is a composite material in which copper or copper alloy is plated with tin or tin-lead alloy. The purpose is to provide a contact with low and stable contact resistance under contact pressure, and a method in which tin or tin-lead alloy is electroplated on copper or copper alloy, and then the plating layer is heated and melted. The degree of variation in plating thickness due to poor wetting of molten tin or molten tin-lead alloy during heating and melting, that is, the difference between the maximum and minimum values of the plating layer thickness, is 0.07 to 0.3 μm per cm 2 . This is a method for manufacturing a contactor. Various types of copper alloys such as phosphor bronze, brass, nickel silver, beryllium copper, and titanium copper are used as the copper alloy, but in the present invention, these copper alloys are coated with tin or tin directly or after being plated with a copper undercoat. - Electroplating lead alloys. Next, this is maintained at a temperature higher than the melting point of tin or tin-lead alloy, and when the thickness of the copper-tin alloy layer and the degree of wettability reach the desired state, it is cooled with water. The conditions for copper undercoat plating, tin plating, and tin-lead alloy plating are well known, and can be appropriately selected from these. Tin-lead alloy plating is generally called solder plating, and is 90wt% tin - 10wt% lead or 60wt% tin.
Those with a composition of 40wt% lead are most often used. In addition to a direct-fired furnace using heavy oil, butane, or the like, an electric furnace, an infrared furnace, a high-frequency heating furnace, or the like may be used for the heating and melting treatment, and the present invention is not limited by these. When a tin or tin-lead alloy layer on copper or copper alloy is heated and melted, one of the accompanying phenomena is "wetting failure". This is also called "dewetting" or "repelling" and occurs when molten tin or tin-lead alloy aggregates into small droplets due to poor wetting with the base material or substrate. Since defective wetting is unfavorable from the viewpoint of quality such as appearance and solderability, many attempts have been made to suppress its occurrence. However, in the present invention, from the viewpoint of contactability,
It has been found that nonuniform plating thickness due to poor wetting is rather preferable. The range is from 0.07 per cm2
0.3 μm is appropriate. If it is less than 0.07 μm, the effect will be low, and if it is more than 0.3 μm, the appearance will deteriorate significantly, which is not preferable. When the non-uniformity of the plating thickness is within the above range, it is considered that an effect of reducing boundary resistance and concentrated resistance occurs at the contact portion of the contact. When tin or tin-lead alloy layer on copper or copper alloy is heated and melted, Cu 6 Sn 5 phase, Cu 3 Sn phase and other matrix are formed as diffusion products between base metal or underlying copper and tin in plating layer. A copper-tin alloy layer containing the material element is formed. Normally, even if the plating layer is water-cooled and solidified immediately after melting, an alloy layer with a thickness of about 0.1 to 0.3 μm is produced, but if this is held in the molten state for several seconds to more than 10 seconds, the thickness of the alloy layer becomes 0.4 to 1.2 μm. It becomes μm. The Vickers hardness of these formed alloy layers is
It has a hardness of 350 to 450, which is significantly harder than the tin or tin-lead alloy layer remaining above it, which has a hardness of 50 or less. Therefore, it is thought that a thin film metal lubrication effect is generated by both layers, and when they are brought into contact with each other by applying contact pressure as an electric contact, sliding or fitting is smooth and the contact resistance is low. Such an effect is not observed when the thickness of the alloy layer is less than 0.4 μm. If it exceeds 1.2 μm, the contact resistance is good, but the appearance tends to deteriorate, making it undesirable as a contact material. Tin or tin-lead alloy plating, which is applied directly to the copper alloy base material without the copper undercoat plating, is preferable because poor wetting conditions can be adjusted by plating pretreatment. In addition, the base material is phosphor bronze (1 to 8 wt% tin, phosphorus).
0.03 to 0.35 wt%), the growth of the alloy layer is rapid, and when used as a contact, the contact resistance is low and stable compared to conventional products. [Example] Copper, German silver, and phosphor bronze plates with a thickness of 0.2 mm were subjected to alkaline degreasing, electrolytic degreasing, and pickling neutralization, followed by electroplating. Various plating conditions are as follows. Copper plating bath composition: Copper sulfate 240g/sulfuric acid 80g/bath temperature: 30℃ Current density: 5A/dm 2Tanning bath composition: tinnous sulfate 60g/sulfuric acid 70g/additive 15g/bath temperature: 20 °C Current density: 2A/dm 2Solder (tin-lead alloy) plating bath composition: Lead borofluoride 54g/tin borofluoride 130g/borofluoric acid 90g/additive 30g/Bath temperature: 20℃ Current density: 5A/dm 2Electrical The heating and melting process after plating is carried out in an electric furnace at 600°C.
The copper-
After forming the tin alloy layer, it was cooled with water and dried with hot air.
The thickness of the copper-tin alloy layer was determined by an electrolytic thickness measurement method. The contact resistance was measured by moving a platinum ring with a radius of 5 mm, loaded with a load of 50 g, on the sample surface and reciprocating it over a distance of 5 mm at a speed of 10 mm/min, passing a direct current of 10 mA, and measuring the contact resistance. The number of round trips was 500. Contact resistance varies with movement and reciprocation, so it is shown as a range. At that time, a strain gauge was brought into contact with the sample to measure the frictional resistance, which was expressed in relative magnitude. The results are shown in Table 1. As is clear from the results in Table 1, the contact resistance of the example is lower than that of the comparative example.
And there are few fluctuations. Furthermore, the frictional resistance is low, so
It is suitable as a composition for contacts.
【表】
[発明の効果]
本発明によれば、接触抵抗が低く、かつ変動も
少く、さらに摩擦抵抗も低い接触子としての特性
が優れた材料が得られる。[Table] [Effects of the Invention] According to the present invention, a material with low contact resistance, little fluctuation, and low frictional resistance and excellent properties as a contactor can be obtained.
Claims (1)
きした後、該めつき層を加熱溶融する方法におい
て、加熱溶融時に溶融錫又は溶融錫−鉛合金のぬ
れ不良現象によるめつき厚みの最大値と最小値の
差が1cm2当り0.07〜0.3μmとすることを特徴とす
る接触子の製造方法。 2 加熱溶融時にめつき層中の錫原子と母材又は
下地の銅原子との拡散により形成される合金層の
厚みが0.4〜1.2μmである特許請求の範囲第1項
記載の接触子の製造方法。 3 銅合金としてりん青銅を用いる特許請求の範
囲第1項又は第2項記載の接触子の製造方法。[Scope of Claims] 1. In a method of electroplating tin or a tin-lead alloy on copper or a copper alloy and then heating and melting the plating layer, poor wetting of the molten tin or the molten tin-lead alloy occurs during heating and melting. A method for manufacturing a contact, characterized in that the difference between the maximum value and the minimum value of plating thickness due to the phenomenon is 0.07 to 0.3 μm per cm 2 . 2. Manufacture of a contact according to claim 1, wherein the alloy layer formed by diffusion of tin atoms in the plating layer and copper atoms of the base material or base material during heating and melting has a thickness of 0.4 to 1.2 μm. Method. 3. A method for manufacturing a contact according to claim 1 or 2, using phosphor bronze as the copper alloy.
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP18357987A JPS6430125A (en) | 1987-07-24 | 1987-07-24 | Manufacture of contactor |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP18357987A JPS6430125A (en) | 1987-07-24 | 1987-07-24 | Manufacture of contactor |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| JPS6430125A JPS6430125A (en) | 1989-02-01 |
| JPH0467726B2 true JPH0467726B2 (en) | 1992-10-29 |
Family
ID=16138283
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP18357987A Granted JPS6430125A (en) | 1987-07-24 | 1987-07-24 | Manufacture of contactor |
Country Status (1)
| Country | Link |
|---|---|
| JP (1) | JPS6430125A (en) |
Families Citing this family (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JP4247339B2 (en) * | 2002-01-21 | 2009-04-02 | Dowaメタルテック株式会社 | Sn-coated member and manufacturing method thereof |
| JP4112426B2 (en) * | 2003-05-14 | 2008-07-02 | 三菱伸銅株式会社 | Method for manufacturing plating material |
-
1987
- 1987-07-24 JP JP18357987A patent/JPS6430125A/en active Granted
Also Published As
| Publication number | Publication date |
|---|---|
| JPS6430125A (en) | 1989-02-01 |
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