JPH042738A - Electrical part, copper alloy for it, and manufacture thereof - Google Patents
Electrical part, copper alloy for it, and manufacture thereofInfo
- Publication number
- JPH042738A JPH042738A JP2103265A JP10326590A JPH042738A JP H042738 A JPH042738 A JP H042738A JP 2103265 A JP2103265 A JP 2103265A JP 10326590 A JP10326590 A JP 10326590A JP H042738 A JPH042738 A JP H042738A
- Authority
- JP
- Japan
- Prior art keywords
- weight
- cold rolling
- copper
- alloy
- hours
- 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
- 229910000881 Cu alloy Inorganic materials 0.000 title claims description 16
- 238000004519 manufacturing process Methods 0.000 title claims description 7
- 229910045601 alloy Inorganic materials 0.000 claims abstract description 33
- 239000000956 alloy Substances 0.000 claims abstract description 33
- 238000005097 cold rolling Methods 0.000 claims abstract description 24
- RYGMFSIKBFXOCR-UHFFFAOYSA-N Copper Chemical compound [Cu] RYGMFSIKBFXOCR-UHFFFAOYSA-N 0.000 claims abstract description 16
- 239000010949 copper Substances 0.000 claims abstract description 16
- 229910052802 copper Inorganic materials 0.000 claims abstract description 15
- 238000005098 hot rolling Methods 0.000 claims abstract description 14
- 238000000137 annealing Methods 0.000 claims abstract description 11
- 229910052725 zinc Inorganic materials 0.000 claims abstract description 11
- 229910052726 zirconium Inorganic materials 0.000 claims abstract description 10
- 238000011282 treatment Methods 0.000 claims abstract description 9
- 238000000034 method Methods 0.000 claims abstract description 8
- 229910052710 silicon Inorganic materials 0.000 claims abstract description 8
- 229910052782 aluminium Inorganic materials 0.000 claims abstract description 7
- 238000010438 heat treatment Methods 0.000 claims abstract description 7
- 230000006698 induction Effects 0.000 claims abstract description 7
- 230000008569 process Effects 0.000 claims abstract description 7
- 229910052759 nickel Inorganic materials 0.000 claims abstract description 6
- PXHVJJICTQNCMI-UHFFFAOYSA-N Nickel Chemical compound [Ni] PXHVJJICTQNCMI-UHFFFAOYSA-N 0.000 claims description 15
- 239000011701 zinc Substances 0.000 claims description 11
- HCHKCACWOHOZIP-UHFFFAOYSA-N Zinc Chemical compound [Zn] HCHKCACWOHOZIP-UHFFFAOYSA-N 0.000 claims description 10
- QCWXUUIWCKQGHC-UHFFFAOYSA-N Zirconium Chemical compound [Zr] QCWXUUIWCKQGHC-UHFFFAOYSA-N 0.000 claims description 8
- XAGFODPZIPBFFR-UHFFFAOYSA-N aluminium Chemical compound [Al] XAGFODPZIPBFFR-UHFFFAOYSA-N 0.000 claims description 6
- 239000010703 silicon Substances 0.000 claims description 6
- 230000008018 melting Effects 0.000 claims description 4
- 238000002844 melting Methods 0.000 claims description 4
- OAICVXFJPJFONN-UHFFFAOYSA-N Phosphorus Chemical compound [P] OAICVXFJPJFONN-UHFFFAOYSA-N 0.000 description 7
- 239000000463 material Substances 0.000 description 7
- 229910000906 Bronze Inorganic materials 0.000 description 6
- 239000010974 bronze Substances 0.000 description 6
- KUNSUQLRTQLHQQ-UHFFFAOYSA-N copper tin Chemical compound [Cu].[Sn] KUNSUQLRTQLHQQ-UHFFFAOYSA-N 0.000 description 6
- ATJFFYVFTNAWJD-UHFFFAOYSA-N Tin Chemical compound [Sn] ATJFFYVFTNAWJD-UHFFFAOYSA-N 0.000 description 5
- 230000006872 improvement Effects 0.000 description 5
- 230000009467 reduction Effects 0.000 description 5
- XUIMIQQOPSSXEZ-UHFFFAOYSA-N Silicon Chemical compound [Si] XUIMIQQOPSSXEZ-UHFFFAOYSA-N 0.000 description 4
- 238000005275 alloying Methods 0.000 description 4
- DMFGNRRURHSENX-UHFFFAOYSA-N beryllium copper Chemical compound [Be].[Cu] DMFGNRRURHSENX-UHFFFAOYSA-N 0.000 description 4
- 238000005336 cracking Methods 0.000 description 4
- 239000000203 mixture Substances 0.000 description 4
- 229910052790 beryllium Inorganic materials 0.000 description 3
- ATBAMAFKBVZNFJ-UHFFFAOYSA-N beryllium atom Chemical compound [Be] ATBAMAFKBVZNFJ-UHFFFAOYSA-N 0.000 description 3
- 229910052751 metal Inorganic materials 0.000 description 3
- 239000002184 metal Substances 0.000 description 3
- 230000002441 reversible effect Effects 0.000 description 3
- 238000005204 segregation Methods 0.000 description 3
- 239000006104 solid solution Substances 0.000 description 3
- 230000000930 thermomechanical effect Effects 0.000 description 3
- XEEYBQQBJWHFJM-UHFFFAOYSA-N Iron Chemical compound [Fe] XEEYBQQBJWHFJM-UHFFFAOYSA-N 0.000 description 2
- 230000003247 decreasing effect Effects 0.000 description 2
- 230000001627 detrimental effect Effects 0.000 description 2
- 230000000694 effects Effects 0.000 description 2
- 238000000265 homogenisation Methods 0.000 description 2
- 239000011159 matrix material Substances 0.000 description 2
- 238000003303 reheating Methods 0.000 description 2
- 238000007711 solidification Methods 0.000 description 2
- 230000008023 solidification Effects 0.000 description 2
- 230000007704 transition Effects 0.000 description 2
- 229910000952 Be alloy Inorganic materials 0.000 description 1
- 229910017532 Cu-Be Inorganic materials 0.000 description 1
- 238000003917 TEM image Methods 0.000 description 1
- 239000000654 additive Substances 0.000 description 1
- 239000003795 chemical substances by application Substances 0.000 description 1
- TVZPLCNGKSPOJA-UHFFFAOYSA-N copper zinc Chemical compound [Cu].[Zn] TVZPLCNGKSPOJA-UHFFFAOYSA-N 0.000 description 1
- 239000012467 final product Substances 0.000 description 1
- 239000010419 fine particle Substances 0.000 description 1
- 230000005802 health problem Effects 0.000 description 1
- 239000004615 ingredient Substances 0.000 description 1
- 229910052742 iron Inorganic materials 0.000 description 1
- 229910001338 liquidmetal Inorganic materials 0.000 description 1
- 238000003754 machining Methods 0.000 description 1
- 230000007246 mechanism Effects 0.000 description 1
- 238000000879 optical micrograph Methods 0.000 description 1
- 239000002245 particle Substances 0.000 description 1
- 229910052698 phosphorus Inorganic materials 0.000 description 1
- 239000011574 phosphorus Substances 0.000 description 1
- 239000004848 polyfunctional curative Substances 0.000 description 1
- 239000000047 product Substances 0.000 description 1
- 239000002994 raw material Substances 0.000 description 1
- 238000005096 rolling process Methods 0.000 description 1
- 230000000087 stabilizing effect Effects 0.000 description 1
- 238000005728 strengthening Methods 0.000 description 1
- 239000000126 substance Substances 0.000 description 1
- 238000003466 welding Methods 0.000 description 1
Landscapes
- Manufacture Of Switches (AREA)
- Contacts (AREA)
- Conductive Materials (AREA)
Abstract
Description
【発明の詳細な説明】
〔産業上の利用分野〕
本発明は、電気部品及び電子部品用の銅合金に関し、さ
らに詳しくは、コネクターやばね用途用の良好なはね特
性を有する新規かつ改良された銅合金、並びにこのよう
な新規かつ改良された銅合金の製造方法に関する。DETAILED DESCRIPTION OF THE INVENTION [Field of Industrial Application] The present invention relates to copper alloys for electrical and electronic components, and more particularly to new and improved copper alloys with good spring properties for connector and spring applications. The present invention relates to copper alloys and methods for producing such new and improved copper alloys.
〔従来の技術と発明が解決しようとする課題〕コネクタ
ー類、ばね類、リレー類、接点類、及びスイッチ類など
の電気部品及び電子部品に用いられる材料は、高い強度
と良好なばね特性を有することが要求される。高強度の
銅基合金は現在用いられており、最も広範に用いられて
いる銅基台金はリン青銅(CDA510.0DA511
)及びベリリウム銅合金(CDA172゜CDA175
)である。[Prior art and problems to be solved by the invention] Materials used for electrical and electronic components such as connectors, springs, relays, contacts, and switches have high strength and good spring characteristics. This is required. High-strength copper-based alloys are currently in use, with the most widely used copper-based metal being phosphor bronze (CDA510.0DA511
) and beryllium copper alloy (CDA172°CDA175
).
リン青銅は比較的高含量(5重量%)のスズを含有する
の−で、凝固中のスズの偏析のために製造プロセスが困
難である。さらに、リン青銅のコストは、複雑な製造プ
ロセスに加えて高価なスズ成分の高含量のために高い。Since phosphor bronze contains a relatively high content of tin (5% by weight), the manufacturing process is difficult due to the segregation of tin during solidification. In addition, the cost of phosphor bronze is high due to the complex manufacturing process as well as the high content of expensive tin components.
スズ成分の偏析は凝固中最小にされねばならず、また圧
延条件は熱機械的処理中のクラック発生を避けるように
注意深く制御されねばならない。しかしながら、リン青
銅(CDA510)の機械的性質は、電気部品用途につ
いてベリリウム銅合金のそれよりも劣っている。Segregation of the tin component must be minimized during solidification and rolling conditions must be carefully controlled to avoid cracking during thermomechanical processing. However, the mechanical properties of phosphor bronze (CDA510) are inferior to those of beryllium copper alloys for electrical component applications.
ベリリウム銅合金は良好な電気伝導度及び熱伝導度と共
に優れた機械的性質を有するけれども、これらの合金の
コストはそのベリリウム含量のために非常に高い。また
、ベリリウム合金は使用されるときに健康を冒す問題を
生じ、べ′リリウムの存在のために全ての溶融、粉砕、
機械加工及び溶接作業について適正な安全対策が図られ
ねばならない。Although beryllium copper alloys have excellent mechanical properties along with good electrical and thermal conductivity, the cost of these alloys is very high due to their beryllium content. Also, beryllium alloys pose health problems when used, and due to the presence of beryllium, all melting, crushing,
Appropriate safety measures must be taken for machining and welding operations.
先行技術の銅合金の一つは特開昭52−5219号公報
に開示されている。しかしながら、この特定の合金は引
張り強さ及び延性における増大は示さない。先行技術の
銅合金の第2のものが特開昭80−59015号公報に
開示されている。この合金は増大した引張り強さを示す
が、リンの添加を必要とする。最後に、第3の先行技術
の銅合金が特開昭59−25935号公報に開示されて
いる。One prior art copper alloy is disclosed in JP-A-52-5219. However, this particular alloy does not exhibit an increase in tensile strength and ductility. A second prior art copper alloy is disclosed in JP-A-80-59015. This alloy exhibits increased tensile strength, but requires the addition of phosphorus. Finally, a third prior art copper alloy is disclosed in JP-A-59-25935.
この合金は増大した引張り強さよりもむしろ高い耐摩耗
性を有するが、亜鉛、ジルコニウム及び鉄添加物の使用
が必要である。This alloy has high wear resistance rather than increased tensile strength, but requires the use of zinc, zirconium and iron additives.
本発明の目的は、高い強度とばね特性を有するが、高価
な合金成分を使用する必要のない新規な低コストで高性
能の銅合金を開発することにある。It is an object of the present invention to develop a new low-cost, high-performance copper alloy that has high strength and spring properties, but does not require the use of expensive alloying components.
本発明によれば、前記目的を達成するために、亜鉛20
〜27重量%、アルミニウム2.0〜5.0重量%、ニ
ッケル0.5〜5.0重量%、珪素0.1〜1.0重量
%、ジルコニウム0゜01〜0.5重量%及び残部銅か
ら成る高強度及び優れたばね特性を有する銅合金が提供
される。According to the present invention, in order to achieve the above object, zinc 20
-27% by weight, aluminum 2.0-5.0% by weight, nickel 0.5-5.0% by weight, silicon 0.1-1.0% by weight, zirconium 0°01-0.5% by weight, and the balance A copper alloy comprising copper having high strength and excellent spring properties is provided.
さらに本発明によれば、(A)亜鉛20〜27重量%、
アルミニウム2.0〜5.0重量%、ニッケル0.5〜
5.0重量%、珪素0.1〜1.0重量%、ジルコニウ
ム0.01〜065重量%及び残部銅から成る銅基合金
を還元性雰囲気下で誘導炉内で溶融し、溶融温度が11
00〜1200℃のときに溶融金属を型内に注入し、(
B)850〜900℃で1〜6時間均質化し、800〜
850℃で熱間圧延し、
(C)熱間圧延後550〜660℃、1〜5時間の条件
で熱処理して単一FCCα相を生成させ、
(D)熱間圧延後の厚さが50%以上減少するように冷
間圧延し、
(E)上記冷間圧延の間に450〜500℃、1〜3時
間の条件で焼なまし処理を施して非常に小さな粒径を生
成させ、
(F)上記最終冷間圧延工程後に、優れたばね特性を生
ずるように200〜300℃で30〜60分間低温応力
除去焼なまし処理を施す各工程からなる高強度及び優れ
たばね特性を有する銅基合金の製造方法が提供される。Furthermore, according to the present invention, (A) 20 to 27% by weight of zinc;
Aluminum 2.0~5.0% by weight, Nickel 0.5~
A copper-based alloy consisting of 5.0% by weight, 0.1 to 1.0% by weight of silicon, 0.01 to 065% by weight of zirconium, and the balance copper was melted in an induction furnace under a reducing atmosphere to a melting temperature of 11% by weight.
Molten metal is injected into the mold at a temperature of 00 to 1200℃, (
B) Homogenize at 850-900°C for 1-6 hours, 800-900°C
Hot rolled at 850°C, (C) Heat treated at 550 to 660°C for 1 to 5 hours after hot rolling to produce a single FCCα phase, (D) Thickness after hot rolling is 50°C. (E) During the cold rolling, annealing is performed at 450 to 500°C for 1 to 3 hours to produce a very small grain size. F) Copper-based alloy with high strength and excellent spring properties, which consists of each step of performing low-temperature stress relief annealing treatment at 200 to 300°C for 30 to 60 minutes to produce excellent spring properties after the final cold rolling process. A manufacturing method is provided.
有利なことに、本発明を用いることにより、スズやベリ
リウムなどの高価な合金成分の使用を完全に省くことが
できる。その代り、多量の亜鉛やアルミニウムなどの安
価な合金成分がコスト低減のために主要合金成分として
添加される。また、少量の珪素やジルコニウムなどのミ
クロ合金成分(1重量%以下)が粒度改善のために添加
される。重要なことに、粒度改善により優れた強度と延
性を得るために最適の熱機械的製造方法が採用され、ま
た好適な熱処理を適用することにより優れたばね特性が
得られる。Advantageously, by using the present invention, the use of expensive alloying components such as tin and beryllium can be completely omitted. Instead, large amounts of inexpensive alloying components such as zinc and aluminum are added as the main alloying component to reduce cost. Additionally, small amounts of microalloy components (1% by weight or less) such as silicon and zirconium are added to improve grain size. Importantly, optimal thermomechanical manufacturing methods are employed to obtain superior strength and ductility due to grain size improvement, and superior spring properties are obtained by applying suitable heat treatments.
ストリップ又はシート製品の製造に本発明を利用すると
きには、冷間圧延が採用される。冷間圧延を可能にする
ためには、ベース母材(マトリックス)については面心
立方(F CC)構造を用いることが望ましい。最終製
品の強度を増強するためには、幾つかの固溶体硬化成分
を、銅−亜鉛系中の体心立方(B CC)などの第2相
を形成することなく、FCCマトリックスに添加するこ
とができる。粘度改善、冷間圧延、及び固溶体硬化など
の各種強化機構を重畳することにより、非常に高い強度
を得ることができる。良好なばね特性は、最終冷間圧延
プロセス後の応力除去熱処理により達成することができ
る。When utilizing the present invention to produce strip or sheet products, cold rolling is employed. To enable cold rolling, it is desirable to use a face-centered cubic (FCC) structure for the base matrix. To enhance the strength of the final product, some solid solution hardening components can be added to the FCC matrix without forming a second phase, such as body-centered cubic (BCC) in copper-zinc systems. can. Very high strength can be obtained by combining various strengthening mechanisms such as viscosity improvement, cold rolling, and solid solution hardening. Good spring properties can be achieved by stress relief heat treatment after the final cold rolling process.
Zn20〜27重量%、Ai)2〜5重量%、NiO,
5〜5.0重量%、Si0.1〜1.0重量%、及びZ
r0.01〜0.5重量%から成る銅基合金は誘導炉で
溶融される。鋳造インゴットは、熱間圧延の前に850
〜900℃で1〜6時間均質化熱処理される。熱間圧延
のために、インゴットスラブは800〜850″に再加
熱され、次いで可逆熱間圧延機を用いて熱間圧延される
。熱間圧延されたプレートは、冷間圧延の前に所望のF
CCα相を生成するために550〜660℃で1〜5時
間焼なましされる。焼なましされた熱間圧延ストリップ
は、次いで可逆冷間圧延機を用いて冷間圧延される。Zn20-27% by weight, Ai) 2-5% by weight, NiO,
5 to 5.0 wt%, Si0.1 to 1.0 wt%, and Z
A copper-based alloy consisting of r0.01-0.5% by weight is melted in an induction furnace. The cast ingot was rolled at 850 ml before hot rolling.
Homogenization heat treatment at ~900°C for 1-6 hours. For hot rolling, the ingot slab is reheated to 800-850" and then hot rolled using a reversible hot rolling mill. The hot rolled plate is rolled to the desired shape before cold rolling. F
Annealed at 550-660°C for 1-5 hours to produce CCα phase. The annealed hot rolled strip is then cold rolled using a reversible cold rolling mill.
本発明の銅合金は熱間圧延並びに冷間圧延において良好
な二次成形適性を示した。冷間圧延プロセスの間、スト
リップは厚さが約50%減少した後450〜500℃で
1〜3時間焼なましされた。熱機械的処理により合金の
強度増大並びに延性のための微粒構造が生ずる。合金は
、冷間圧延ストリップにおいても使用でき、あるいはば
ね特性を増大するために200〜300℃で30〜60
分応力除去熱処理に付することもできる。The copper alloy of the present invention showed good suitability for secondary forming in hot rolling as well as cold rolling. During the cold rolling process, the strips were annealed at 450-500 °C for 1-3 hours after the thickness was reduced by about 50%. The thermomechanical treatment creates a fine grain structure for increased strength and ductility of the alloy. The alloy can also be used in cold rolled strip or rolled at 30-60°C at 200-300°C to increase spring properties.
It can also be subjected to stress relief heat treatment.
合金成分及びその制限:
亜鉛の添加(20〜27重量%)は、本発明合金のコス
ト低減のために主たる固溶体硬化材としてなされた。亜
鉛が27重量%を越えると、二相の転移が生じ得、すな
わちα相FCCとBCCβ相であり、これらはいずれも
延性にとって有害である。一方、亜鉛含量が20重量%
未満であると、合金は充分な強度を示さなくなる。Alloy Ingredients and Limitations: Zinc addition (20-27% by weight) was made as the main solid solution hardener to reduce the cost of the invention alloy. Above 27% by weight zinc, a two-phase transition can occur, namely the alpha phase FCC and the BCC beta phase, both of which are detrimental to ductility. On the other hand, the zinc content is 20% by weight.
If it is less than that, the alloy will not exhibit sufficient strength.
本発明の合金にはAgが添加される(2〜5重量%)。Ag is added to the alloy of the invention (2-5% by weight).
Al1量が5重量%を越えると、冷間圧延を行なうこと
が困難となり、また低延性となることが見い出された。It has been found that when the amount of Al1 exceeds 5% by weight, cold rolling becomes difficult and ductility becomes low.
逆に、2重量%未満のAII量であれば所望の高強度が
得られなくなる。Conversely, if the amount of AII is less than 2% by weight, the desired high strength cannot be obtained.
Niの添加(0,5〜5重量%)は合金の延性を改善す
るためになされた。NiはFCCα相安定化成分であり
、Cu−Zn−Al −X系へのAffの溶解性を拡大
する。Ni成分が0.5重量%未満であれば延性改善が
充分でなく、方、Ni成分が5重量%を越えると得られ
る合金のコストが非経済的となる。The addition of Ni (0.5-5% by weight) was made to improve the ductility of the alloy. Ni is an FCCα phase stabilizing component and expands the solubility of Aff in the Cu-Zn-Al-X system. If the Ni content is less than 0.5% by weight, the improvement in ductility will not be sufficient, while if the Ni content exceeds 5% by weight, the cost of the resulting alloy will become uneconomical.
Siの添加(0,1〜1.0重量%)は、粒度改善のた
めに、また強度を上げるためになされた。Si量が0.
1重量%未満であると微細粒径又は十分な強度が得られ
なかった。逆に、Si量が1重量%を越えると延性の改
善に有害であった。Addition of Si (0.1-1.0% by weight) was made to improve grain size and increase strength. The amount of Si is 0.
If it was less than 1% by weight, fine particle size or sufficient strength could not be obtained. On the other hand, if the amount of Si exceeded 1% by weight, it was detrimental to the improvement of ductility.
Zrの添加(0,01〜0.5重量%)は、良好な延性
と併せて高強度を達成するために、粒度をさらに下げる
ために非常に重要であった。The addition of Zr (0.01-0.5 wt%) was very important to further reduce the grain size in order to achieve high strength together with good ductility.
ZrとStを同時に添加することにより、高強度と二次
成形適性を有する非常に小さな粒度が得られた。Zrが
0.01重量%未満であると粒度改善が充分でなく、一
方、Zr成分が0.5重量%を越えるとα相の可能な粒
界偏析が生ずることが見い出された。By adding Zr and St simultaneously, a very small particle size with high strength and forming suitability was obtained. It has been found that if the Zr content is less than 0.01% by weight, grain size improvement is not sufficient, while if the Zr content exceeds 0.5% by weight, possible grain boundary segregation of the α phase occurs.
製造プロセス:
Z n 20〜27重量%、A472〜5重量%、Ni
O,5〜5.0重量%、SiO,1〜1.0重量%及び
ZrO,01〜0.5重量%からなる本発明の銅合金は
、還元性雰囲気下で誘導炉内で溶融される。電気銅、亜
鉛、アルミニウム及びニッケルの市販の純粋な原料が用
いられる。Manufacturing process: Zn 20-27% by weight, A472-5% by weight, Ni
The copper alloy of the present invention, consisting of O, 5-5.0% by weight, SiO, 1-1.0% by weight and ZrO, 01-0.5% by weight, is melted in an induction furnace under a reducing atmosphere. . Commercial pure raw materials of electrolytic copper, zinc, aluminum and nickel are used.
純粋な珪素およびジルコニウムが添加される。Pure silicon and zirconium are added.
溶融温度が1100〜1200℃のときに、溶融金属を
型内に注入する。鋳造インゴットは熱間圧延の前に85
0〜900℃で1〜6時間均質化される。800〜85
0℃で1〜2時間インゴットを再加熱した後、インゴッ
トを可逆熱間圧延機により熱間圧延する。所望の厚さに
達したときに、インゴットを室温に冷却する。α−相で
平衡を有する均質な構造を得るために、熱間圧延された
プレートを550〜660℃で1〜5時間焼なましし、
引き続き塵冷する。焼なましされたプレートは、次いで
クラックを生ずることなく冷間圧延プロセスに付され、
それにより本発明の合金にとって良好な冷間圧延成形性
を示す。冷間圧延により約70%減少した後、冷間スト
リップを450〜500℃で1〜3時間焼なましし、さ
らに厚みを減少させる。The molten metal is poured into the mold when the melting temperature is 1100-1200°C. The cast ingot is heated to 85% before hot rolling.
Homogenize at 0-900°C for 1-6 hours. 800-85
After reheating the ingot at 0° C. for 1 to 2 hours, the ingot is hot rolled using a reversible hot rolling mill. When the desired thickness is reached, the ingot is cooled to room temperature. In order to obtain a homogeneous structure with equilibrium in the α-phase, the hot-rolled plate was annealed at 550-660 °C for 1-5 hours,
Continue to cool down. The annealed plate is then subjected to a cold rolling process without cracking,
This shows good cold rolling formability for the alloy of the invention. After about 70% reduction by cold rolling, the cold strip is annealed at 450-500° C. for 1-3 hours to further reduce the thickness.
最終的に冷間圧延されたストリップを、応用除去のため
に 200〜300℃で0.5〜1時間時間表ししてば
ね特性を増大させる。The final cold-rolled strip is exposed for application removal at 200-300° C. for 0.5-1 hour to increase spring properties.
以下、実施例を示して本発明についてさらに具体的に説
明する。Hereinafter, the present invention will be described in more detail with reference to Examples.
実施例1
表−1に示す化学組成の合金(No、1.2゜3.4.
5)を高周波誘導炉を用いて溶融した。Example 1 An alloy having the chemical composition shown in Table 1 (No. 1.2°3.4.
5) was melted using a high frequency induction furnace.
1150℃の液状金属を50 X 50 X 130
mmの寸法を有する型内に注入した。Liquid metal at 1150℃ 50 x 50 x 130
It was poured into a mold having dimensions of mm.
インゴットを900℃で1時間均質化し、850℃で熱
間圧延した。熱間圧延したプレートを550℃で5時間
焼なましした。焼なまししたプレートを冷間圧延して5
0%減少させた。The ingot was homogenized at 900°C for 1 hour and hot rolled at 850°C. The hot rolled plate was annealed at 550°C for 5 hours. Cold rolling the annealed plate 5
Reduced by 0%.
冷間圧延プロセスの間に500’Cで1時間中間焼なま
し処理を施した。最終プレートを、ばね特性を強化する
ために250”Cで1時間焼なましした。An intermediate annealing treatment was performed at 500'C for 1 hour during the cold rolling process. The final plate was annealed at 250”C for 1 hour to enhance its spring properties.
得られた本発明の合金No、5(第3図における“PM
C−707”)の機械的性質をリン青銅CDA310及
びCu−Be合金CDA175、CDA172のそれと
比較した。その結果を第3図に示す。本発明の合金はC
DA310よりも強度が大きいがCDA−172よりも
劣っている。冷間圧延シートへの最終焼なまし処理によ
りばね特性値は33kg/mm2がら80 kg /
m+g 2に増大する。The obtained alloy No. 5 of the present invention (“PM” in Fig. 3)
The mechanical properties of C-707'') were compared with those of phosphor bronze CDA310 and Cu-Be alloys CDA175 and CDA172. The results are shown in Figure 3.
It has greater strength than DA310 but is inferior to CDA-172. Due to the final annealing treatment on the cold-rolled sheet, the spring characteristic value decreased from 33 kg/mm2 to 80 kg/mm2.
Increases to m+g 2.
実施例2
表−2の合金(No、6.7)を実施例1と同様に溶融
し鋳造した。Example 2 The alloy shown in Table 2 (No. 6.7) was melted and cast in the same manner as in Example 1.
きであるということは本質的なものである。Being able is essential.
SiとZrを同時に添加することにより、第1図(C)
に示すようにさらに粒度改善を生じ、良好な延性と共に
高い強度が得られた。By adding Si and Zr simultaneously, as shown in Fig. 1 (C)
As shown in Figure 2, the grain size was further improved and high strength was obtained along with good ductility.
第2図は冷間圧延により発現した転位下部構造を示す。Figure 2 shows the dislocation substructure developed by cold rolling.
転位下部構造は高強度にとって本質的なものである。Dislocation substructure is essential for high strength.
実施例3
表−4に示す組成の2つの合金を誘導炉内で溶融し、矩
形型内に鋳込んだ。Example 3 Two alloys having the compositions shown in Table 4 were melted in an induction furnace and cast into a rectangular mold.
インゴットを850℃で6時間均質化した。The ingot was homogenized at 850°C for 6 hours.
均質化されたインゴットを800℃で熱間圧延した。熱
間圧延されたプレートを2つの異なる条件で焼なましし
た。第1の条件は完全FCCα相を得るために550℃
で5時間であり、方、第2の条件はα、β相の混合物を
得るために700℃で1時間であった。焼なましされた
プレートを冷間圧延して完全α相プレートと二元α及び
β相プレートを50%減少させた。50%減少を施した
ときにα+β相材料については冷間クラッキングを生じ
たが、同じ減少(50%)についてα相材料には冷間圧
延クラックは生じなかった。従って、α+β相材料には
35%減少が施された。最終の圧延シートは220℃で
1時間焼なましされた。α+β相材料(35%減少)の
機械的性質は表−3にまとめられている。完全α相のそ
れと比較すると(表−2参照)、α+β相材料の機械的
性質はα相材料のそれよりも劣っている。従って、熱間
圧延後の後焼なまし処理で完全FCCα相転移を生ずべ
850℃で5時間均質化処理した後、インゴットを80
0℃に再加熱後熱間圧延した。熱間圧延したプレートを
、FCCα相の熱力学平衡相を得るために600℃及び
650℃でそれぞれ3時間及び1時間焼なましした。The homogenized ingot was hot rolled at 800°C. The hot rolled plates were annealed under two different conditions. The first condition is 550°C to obtain a complete FCCα phase.
The second condition was 700° C. for 1 hour to obtain a mixture of α and β phases. The annealed plates were cold rolled to reduce the complete α-phase plates and the binary α and β-phase plates by 50%. Cold cracking occurred for the α+β phase material when a 50% reduction was applied, but no cold rolling cracking occurred for the α phase material for the same reduction (50%). Therefore, a 35% reduction was applied to the α+β phase material. The final rolled sheet was annealed at 220° C. for 1 hour. The mechanical properties of the α+β phase material (35% reduction) are summarized in Table-3. When compared with that of the complete α phase (see Table 2), the mechanical properties of the α+β phase material are inferior to those of the α phase material. Therefore, the post-annealing treatment after hot rolling caused complete FCCα phase transition, and after homogenization treatment at 850°C for 5 hours, the ingot was
After reheating to 0°C, hot rolling was performed. The hot-rolled plates were annealed at 600 and 650 °C for 3 and 1 h, respectively, to obtain the thermodynamic equilibrium phase of the FCCα phase.
焼なまししたプレートを、幾行程かで冷間圧延しく60
%及び70%)、上記行程の間に厚さが減少した。The annealed plate is cold rolled in several steps.
% and 70%), the thickness decreased during the above steps.
1次冷間圧延ストリップを500℃及び450℃でそれ
ぞれ1.5時間及び2.5時間焼なましした後、2次冷
間圧延を行なった。The first cold rolled strip was annealed at 500° C. and 450° C. for 1.5 hours and 2.5 hours, respectively, and then subjected to second cold rolling.
低温焼なまし処理の機械的性質に対する効果を調査する
ために、最終冷間圧延ストリップを300℃及び250
℃でそれぞれ30分間及び40分間焼なましした。結果
は表−4にまとめられている。To investigate the effect of low temperature annealing treatment on the mechanical properties, the final cold rolled strip was
Annealed at ℃ for 30 and 40 minutes, respectively. The results are summarized in Table-4.
第1図(A)、(B)及び(C)は、Cu−232n−
3,4AIJ−INiからなる合金への81及びZr添
加の結果を示す合金組織の光学顕微鏡写真である。
第2図は、転位下部構造を示すCu−23Zn−3,4
All−INi−0,3S i−0,IZrからなる合
金の冷間圧延ストリップの透過型電子顕微鏡写真である
。
第3図は、P M C−707として示されている代表
的組成Cu−23Zn−3,4AΩ−INi−0,3S
i−0,IZrの本発明の合金の降伏強さ及び引張り強
さを他の高性能合金、リン青銅CDA310、ベリリウ
ム銅CDA175及びCDA172の合金と比較して示
すグラフである。
出願人 ブーングサン、コーポレーション代理人
弁理士 米 原 正 章Figure 1 (A), (B) and (C) are Cu-232n-
3 is an optical micrograph of an alloy structure showing the result of adding 81 and Zr to an alloy consisting of 3,4AIJ-INi. Figure 2 shows the Cu-23Zn-3,4 dislocation substructure.
1 is a transmission electron micrograph of a cold rolled strip of an alloy consisting of All-INi-0,3S i-0,IZr. Figure 3 shows a typical composition Cu-23Zn-3,4AΩ-INi-0,3S, designated as PMC-707.
1 is a graph showing the yield strength and tensile strength of the i-0, IZr inventive alloy in comparison to other high performance alloys, phosphor bronze CDA310, beryllium copper CDA175 and CDA172 alloys. Applicant Boongsan, Corporation Agent
Patent attorney Masaaki Yonehara
Claims (2)
.0重量%、ニッケル0.5〜5.0重量%、珪素0.
1〜1.0重量%、ジルコニウム0.01〜0.5重量
%及び残部銅から成る高強度及び優れたばね特性を有す
る銅合金。(1) Zinc 20-27% by weight, aluminum 2.0-5%
.. 0% by weight, 0.5-5.0% by weight of nickel, 0.0% of silicon.
A copper alloy with high strength and excellent spring properties consisting of 1-1.0% by weight of zirconium, 0.01-0.5% by weight of zirconium and the balance copper.
0〜5.0重量%、ニッケル0.5〜5.0重量%、珪
素0.1〜1.0重量%、ジルコニウム0.01〜0.
5重量%及び残部銅から成る銅基合金を還元性雰囲気下
で誘導炉内で溶融し、溶融温度が1100〜1200℃
のときに溶融金属を型内に注入し、 (B)850〜900℃で1〜6時間均質化し、800
〜850℃で熱間圧延し、 (C)熱間圧延後550〜660℃、1〜5時間の条件
で熱処理して単一FCCα相を生成させ、 (D)熱間圧延後の厚さが50%以上減少するように冷
間圧延し、 (E)上記冷間圧延の間に450〜500℃、1〜3時
間の条件で焼なまし処理を施して非常に小さな粒径を生
成させ、 (F)上記最終冷間圧延工程後に、優れたばね特性を生
ずるように200〜300℃で30〜60分間低温応力
除去焼なまし処理を施す 各工程からなる高強度及び優れたばね特性を有する銅基
合金の製造方法。(2) (A) 20-27% by weight of zinc, aluminum 2.
0-5.0% by weight, 0.5-5.0% by weight of nickel, 0.1-1.0% by weight of silicon, 0.01-0.0% by weight of zirconium.
A copper-based alloy consisting of 5% by weight and the balance copper is melted in an induction furnace under a reducing atmosphere, and the melting temperature is 1100-1200°C.
(B) Homogenize at 850-900℃ for 1-6 hours,
(C) After hot rolling, heat treatment is performed at 550-660°C for 1-5 hours to produce a single FCCα phase; (D) The thickness after hot rolling is (E) during the cold rolling, annealing is performed at 450 to 500°C for 1 to 3 hours to produce a very small grain size; (F) A copper base with high strength and excellent spring properties, which consists of each step of performing low-temperature stress relief annealing treatment at 200 to 300°C for 30 to 60 minutes to produce excellent spring properties after the final cold rolling process. Alloy manufacturing method.
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP2103265A JPH042738A (en) | 1990-04-20 | 1990-04-20 | Electrical part, copper alloy for it, and manufacture thereof |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP2103265A JPH042738A (en) | 1990-04-20 | 1990-04-20 | Electrical part, copper alloy for it, and manufacture thereof |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| JPH042738A true JPH042738A (en) | 1992-01-07 |
| JPH0565570B2 JPH0565570B2 (en) | 1993-09-20 |
Family
ID=14349601
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP2103265A Granted JPH042738A (en) | 1990-04-20 | 1990-04-20 | Electrical part, copper alloy for it, and manufacture thereof |
Country Status (1)
| Country | Link |
|---|---|
| JP (1) | JPH042738A (en) |
Citations (6)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JPS5432610A (en) * | 1977-08-15 | 1979-03-10 | Kisaku Mori | Extracting of pharmaceutically effective substance of mushrooms |
| JPS5597444A (en) * | 1979-01-16 | 1980-07-24 | Mitsubishi Electric Corp | Copper alloy for spring |
| JPS5687643A (en) * | 1979-12-18 | 1981-07-16 | Tamagawa Kikai Kinzoku Kk | Copper alloy with superior high-duty elasticity and corrosion resistance |
| JPS6059035A (en) * | 1983-09-08 | 1985-04-05 | Furukawa Electric Co Ltd:The | Shape memory cu-zn-al alloy |
| JPS60138032A (en) * | 1983-12-26 | 1985-07-22 | Mitsubishi Metal Corp | Cu-based shape memory alloy |
| JPS6421026A (en) * | 1987-07-16 | 1989-01-24 | Furukawa Electric Co Ltd | Bending-resisting cable conductor |
-
1990
- 1990-04-20 JP JP2103265A patent/JPH042738A/en active Granted
Patent Citations (6)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JPS5432610A (en) * | 1977-08-15 | 1979-03-10 | Kisaku Mori | Extracting of pharmaceutically effective substance of mushrooms |
| JPS5597444A (en) * | 1979-01-16 | 1980-07-24 | Mitsubishi Electric Corp | Copper alloy for spring |
| JPS5687643A (en) * | 1979-12-18 | 1981-07-16 | Tamagawa Kikai Kinzoku Kk | Copper alloy with superior high-duty elasticity and corrosion resistance |
| JPS6059035A (en) * | 1983-09-08 | 1985-04-05 | Furukawa Electric Co Ltd:The | Shape memory cu-zn-al alloy |
| JPS60138032A (en) * | 1983-12-26 | 1985-07-22 | Mitsubishi Metal Corp | Cu-based shape memory alloy |
| JPS6421026A (en) * | 1987-07-16 | 1989-01-24 | Furukawa Electric Co Ltd | Bending-resisting cable conductor |
Also Published As
| Publication number | Publication date |
|---|---|
| JPH0565570B2 (en) | 1993-09-20 |
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