JPH0543774B2 - - Google Patents
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- JPH0543774B2 JPH0543774B2 JP63083674A JP8367488A JPH0543774B2 JP H0543774 B2 JPH0543774 B2 JP H0543774B2 JP 63083674 A JP63083674 A JP 63083674A JP 8367488 A JP8367488 A JP 8367488A JP H0543774 B2 JPH0543774 B2 JP H0543774B2
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Description
産業上の利用分野
この発明は各種電子機器、電気機器等における
導電材料として使用される高導電率アルミニウム
合金に関するものである。
従来の技術
一般に導電用の純アルミニウム系高導電率アル
ミニウム合金としては、JIS H4180で規定される
1060合金や、JIS H4000で規定される1070合金が
広く用いられている。1060合金は、JIS H4180の
規格においてその合金成分含有量がSi0.25%(wt
%、以下同じ)以下、Fe0.35%以下、Cu0.05%以
下、Mn0.03%以下、Mg0.03%以下、Zn0.05%以
下、Ti0.03%以下と定められ、また1070合金は
JIS H4000の規格においてその合金成分含有量が
Si0.20%以下、Fe0.25%以下、Cu0.04%以下、
Mn0.03%以下、Mg0.03%以下、Zn0.04%以下、
Ti0.03%以下と定められている。
ところで一般に導電用の高導電率アルミニウム
合金としては、導電率がIACS%(以下導電率に
ついては全てIACS%で示す)にして61%以上の
ものが要求されている。アルミニウム合金におい
ては、そのうちに含まれる不純物含有量を少なく
すれば、導電率が高くなることが知られている。
実際の導電用アルミニウム合金においては、特に
Cu、Mn、Ti、Vを極微量に規制した高純度電気
用アルミニウム地金を用いて鋳造し、合金中の不
純物元素含有量を少なくしており、またFe量や
Si量も規制し、一般にはSi0.05%程度、Fe0.10%
程度として導電率61.0%以上の材料を得ている。
発明が解決すべき問題点
前述のようにCu、Mn、Ti、Vなどの不純物元
素の含有量やFe、Siの含有量を極力低減すれば
高導電率のアルミニウム合金を得ることかできる
が、やみくもにこれらの量を低減しようとすれ
ば、導電率は高くなつても、地金コストや溶解炉
等の問題から高コスト化を招いてしまう。
この発明は以上の事情を背景としてなされたも
ので、いたずらに高コスト化を招くことなく、導
電率61%以上の高導電率を確実に得ることができ
るアルミニウム合金を提供することを目的とする
ものである。
問題点を解決するための手段
本発明者等が導電率とアルミニウム合金の成分
組成、組織との関係について詳細に検討を重ねた
ところ、単純に不純物量を低減するのではなく、
合金中のFe固溶量、Si固溶量をそれぞれ特定の
値以下とすることによつて、導電率61%以上の高
導電率材料が得られることを見出し、この発明を
なすに至つた。
すなわちこの発明の導電用アルミニウム合金
は、Fe0.04〜0.70wt%、Si0.04〜0.25wt%を含有
し、不可避的不純物を各元素それぞれ0.02wt%以
下、総量で0.05wt%以下に規制し、残部がAlか
らなる成分組成を有し、しかもFeの固溶量が
100ppm以下、Siの固溶量が400ppm以下であるこ
とを特徴とするものである。
作 用
不純物元素含有量を少量に規制したアルミニウ
ム合金の導電率には、マトリツクス中に固溶して
いるFeの量(固溶Fe量)および同じくマトリツ
クス中に固溶しているSiの量(固溶Si量)が大き
く影響し、特に固溶Fe量の影響が大きい。固溶
Siは同じ固溶量で比較すれば固溶Feほどには導
電率に与える影響は大きくないが、SiはFeと比
較して固溶度が大きく、実際の合金中で固溶して
いるSi量も固溶Fe量より格段に多いから、量的
な変動が大きく、そのため固溶Si量も結局は導電
率に大きな影響を及ぼす。固溶Fe量、固溶Si量
が導電率に及ぼす影響を本発明者等が調べたとこ
ろ、合金中に総Fe量や総Si量、その他の不純物
量をかなりの程度まで規制しても、固溶Fe量が
100ppmを越えるかまたは固溶Si量が400ppmを越
えれば、導電率61%以上の材料を安定して得るこ
とが困難であることが判明した。そして逆にFe
の総量やSiの総量がある程度大きくても、固溶
Fe量を100ppm以下としかつ固溶Si量を400ppm
以下とすれば導電率61%以上の材料安定して得る
ことができることが判明した。したがつてこの発
明では固溶Fe量を100ppm以下、固溶Si量を
400ppm以下に規制することにした。
さらにこの発明のアルミニウム合金ではFeの
総量およびSiの総量、不可避的不純物元素量も規
定しており、これらの限定理由について以下に説
明する。
Fe:
Fe量を0.04%未満とすることは著しいコスト上
昇を招く。またFe量が0.7%を越えれば、鋳造法
によつてはFeの強制固溶量が著しく大きくなり、
固溶Fe量を100ppm以下に規制することが困難と
なる。したがつてFeの総量は0.04〜0.7%の範囲
内とした。
Si:
Si量を0.04%未満とすることはFeの場合と同様
に著しいコスト上昇を招く。一方Si量が0.25%を
越えれば、固溶Si量を400ppm以下に抑制するこ
とが困難となる。したがつてSiの総量は0.04〜
0.25%の範囲内とした。
不可避的不純物:
通常のアルミニウム合金においては、Mn、
Ti、Cr、V、Zr、Mg、Cu等が不可避的不純物
として含まれるが、いずれかの不純物元素の単独
含有量が0.02%を越えるか、または合計の含有量
が0.05%を越えれば、前述のように固溶Fe量、固
溶Si量をそれぞれ100ppm以下、400ppm以下に規
制しても、61%以上の導電率を得ることが困難と
なる。したがつて不可避的不純物元素は、それぞ
れ0.02%以下、合計で0.05%以下に規制した。な
お各種不可避的不純物元素のうちでも特にMn、
Ti、Cr、V、Zrは導電率に悪影響を及ぼすから、
これらはそれぞれ0.01%以下とすることが望まし
い。
以上のように、この発明のアルミニウム合金で
は、固溶Fe量を100ppm以下、固溶Si量を
400ppm以下に規制し、併せて不可避的不純物元
素含有量を前述のように規制することによつて、
導電率61%以上の材料を安定して得ることが可能
となつた。
発明の実施のための具体的な説明
この発明のアルミニウム合金は、基本的には固
溶Fe量、固溶Si量をそれぞれ100ppm以下、
400ppm以下に規制していることが重要であるが、
このような固溶Fe量は第1図に示すような分析
方法によつて知得することができ、また固溶Si量
は第2図に示すような分析方法によつて求めた残
渣Si量の総Si量から差引くことにより知得するこ
とができる。
次この発明の導電用アルミニウム合金の製造方
法について説明する。
この発明の導電用アルミニウム合金は前述のよ
うに合金中の固溶Fe量および固溶Si量を規制し
ており、したがつてその製造方法としてもこれら
の固溶量を規制するための方策を講じる必要があ
る。そこで基本的には、前述のような成分組成の
合金鋳塊を熱間圧延するに先立つて300〜550℃に
おいて0.5〜24時間加熱し、熱間圧延後に加工率
50%以上の冷間加工(冷間圧延もしくは線引加工
等)を施し、最終焼鈍として220〜330℃において
0.5〜24時間加熱する方法を適用することが望ま
しい。あるいはまた前記成分組成の合金鋳塊を熱
間圧延するに先立つて前記同様に300〜550℃にお
いて0.5〜24時間加熱し、熱間圧延後に加工率30
%以上の冷間加工と220〜330℃での0.5〜24時間
の中間焼鈍とを1回または2回以上繰返し実施し
た後、加工率50%以上の最終冷間加工を行ない、
その後最終焼鈍として前記同様に220〜330℃にお
いて0.5〜24時間加熱する方法を適用することが
望ましい。
以下にこれらの製造方法についてさらに詳細に
説明する。
先ず前述のようにFe0.04〜0.70%、Si0.04〜
0.25%、その他の不可避的不純物を各元素それぞ
れ0.02%以下、総量で0.05%以下となるように調
整されたアルミニウム合金溶湯を常法にしたがつ
て鋳造し、鋳塊を作成する。ここで常法とは、プ
ロペルチ法や連続鋳造圧延法等による連続鋳造、
あるいはビレツトやスラブのDC鋳造等を意味す
る。
このような鋳塊においては、その冷却速度によ
つても異なるが、Feの固溶量は少なくとも
300ppmを越えており、またSiはその添加量の大
半が固溶している。このようなレベルのFe固溶
量、Si固溶量では当然のことながら導電率が低い
から、固溶していたFe、Siを鋳造後の工程にお
いて析出させて、これらの固溶量を低減させる必
要がある。そのための第1段階として、鋳塊の加
熱および熱間圧延がある。すなわち、熱間圧延に
先立つ鋳塊の加熱を300〜550℃の温度範囲にて
0.5〜24時間保持の条件にて行ない、その後熱間
圧延を行なう。但しこの加熱は、均熱処理として
行なつても、あるいは熱間圧延直前の加熱処理と
して行なつても良い。すなわち予め鋳塊を300〜
550℃×0.5〜24時間の条件で均熱処理した後、再
びその温度範囲に再加熱して熱間圧延に供しても
良く、あるいは鋳塊を300〜550℃×0.5〜24時間
加熱し、そのまま熱間圧延に供しても良い。
上述のように熱間圧延前の加熱を300〜550℃×
0.5〜24時間とする理由は次の通りである。
すなわち、Feは300〜550℃の範囲でその析出
が最大となるから、その温度範囲での加熱により
Feの固溶量を低減することができる。ここで300
℃未満ではFeの析出が不充分でその固溶量を充
分に低減させることができず、一方550℃を越え
ればFeの再固溶が生じてその固溶量が多くなつ
てしまう。またSiは、鋳塊段階では金属Siとして
は析出しないが、300〜550℃の範囲内の温度での
加熱により固溶SiがAl−Fe系の晶出物中に移行
して、αAlFeSi、βAlFeSiとなつたり、Al3Fe
(Si)となつたりし、また析出物もαAlFeSi等と
なり、Feの析出とSiの析出とが共存する。ここ
で300℃未満ではSiの析出も不充分となり、一方
550℃を越えれば晶出物中のSiが再びマトリツク
ス中へ移行し、マトリツクス中のSi固溶量が増大
してしまう。なお鋳塊加熱時間が0.5時間未満で
はFe、Siを析出させる効果が充分に得られず、
一方24時間を越える長時間加熱を行なつてもいた
ずらにコストが増すだけである。したがつて鋳塊
加熱の条件は300〜550℃にて0.5〜24時間とする。
もちろん上述のような鋳塊加熱と熱間圧延の段
階のみでは、固溶Fe量、固溶Si量を目標とする
レベルまで低減させることは困難であるが、その
後の処理に先立つて、上記条件での熱処理により
Fe、Siの固溶レベルを適当なレベルまで下げて
おかなければ、最終的な目標レベルまで低下させ
ることは困難である。
熱間圧延後には冷間圧延や冷間線引加工等の冷
間加工を行ない、その後最終焼鈍を施すが、この
場合の冷間加工は加工率50%以上とし、また最終
焼鈍220〜330℃の範囲内の温度で0.5〜24時間の
加熱とする。これらの冷間圧延および最終焼鈍の
条件も、Fe、Siの析出を促進してその固溶量を
低減させるために重要である。すなわち、Feお
よびSiの析出サイトとしては転位が重要であり、
転移密度を高くすることがFe、Siの析出に寄与
する。したがつて冷間加工度を大きくして転位密
度を高めておくことにより、その後の焼鈍でFe、
Siの析出量を多くし、固溶Fe量、固溶Si量を目
標レベルまで低減させることができる。冷間加工
後の最終焼鈍では、Fe、SiはAlFeSi系析出物と
して析出し、またSiは金属Siとしても析出する。
ここで、冷間加工率が50%未満では転位密度の
上昇が不充分であり、その後の最終焼鈍で充分な
Fe、Siの析出が図れない。また最終焼鈍温度が
220℃未満ではFe、Siの析出が不充分であつて、
特にFeの析出が不充分となり、一方330℃を越え
てもFe、Siの析出が不充分で、特にSiが再固溶
をはじめて、固溶量低減が達成されなくなる。最
終焼鈍の時間が0.5時間未満では上述のようなFe、
Siの析出が充分に行なわれず、一方24時間を越え
る長時間加熱を行なつてもいたずらにコスト増大
を招くだけである。したがつて冷間加工は加工率
50%以上、最終焼鈍の条件は220〜330℃×0.5〜
24時間とした。なお最終焼鈍における加熱速度は
遅いことが好ましく、通常は100℃/hr以下の昇
温速度とすることが望ましい。
またFe、Siの析出をより一層促進させるため
に、熱間圧延後に1次冷間加工と中間焼鈍とを1
回行なうかまたはこれらを2回以上繰返した後、
最終冷間加工し、その後最終焼鈍を施しても良
い。この場合の1次冷間加工は加工率30%以上と
し、中間燃鈍は220〜330℃×0.5〜24時間とする
ことが好ましい。この場合も最終冷間加工は前述
の場合と同様に50%以上とし、最終焼鈍も220〜
330℃×0.5〜24時間とすれば良い。このように冷
間加工による転位速度増大と上記温度範囲での焼
鈍によるFe、Siの析出を繰返すことによつて、
Fe、Siの固溶量を充分に低減させることが可能
となる。
実施例
第1表の合金符号1,2に示す成分組成の合金
をDC鋳造法により厚さ500mm、幅1200mmのスラブ
に鋳造し、そのスラブを第2表中に示す鋳塊加熱
条件で加熱して常法にしたがつて熱間圧延し、厚
さ4mmの熱延板とした。次いでその熱延板を第2
表に示すように冷間圧延−最終焼鈍、もしくは1
次冷間圧延−中間焼鈍−最終冷間圧延−最終焼鈍
の工程にしたがつて処理した。最終焼鈍後の板に
おけるFe固溶量、Si固溶量を既に述べた方法に
より調べるとともに、導電率を調べた。その結果
も第2表中に併せて示す。
INDUSTRIAL APPLICATION FIELD This invention relates to a high conductivity aluminum alloy used as a conductive material in various electronic devices, electrical devices, etc. Conventional technology Pure aluminum-based high conductivity aluminum alloys for electrical conductivity are generally specified in JIS H4180.
1060 alloy and 1070 alloy specified by JIS H4000 are widely used. According to the JIS H4180 standard, 1060 alloy has an alloy component content of 0.25% Si (wt
%, hereinafter the same) or less, Fe0.35% or less, Cu0.05% or less, Mn0.03% or less, Mg0.03% or less, Zn0.05% or less, Ti0.03% or less, and 1070 alloy is
According to the JIS H4000 standard, the alloy component content is
Si0.20% or less, Fe0.25% or less, Cu0.04% or less,
Mn 0.03% or less, Mg 0.03% or less, Zn 0.04% or less,
Ti is defined as 0.03% or less. By the way, high conductivity aluminum alloys for electrical conductivity are generally required to have a conductivity of 61% or more in terms of IACS% (hereinafter all conductivities are expressed in IACS%). It is known that the electrical conductivity of an aluminum alloy increases if the content of impurities contained therein is reduced.
In actual conductive aluminum alloys, especially
It is cast using high-purity electrical aluminum ingots containing extremely small amounts of Cu, Mn, Ti, and V, reducing the content of impurity elements in the alloy, and reducing the amount of Fe.
The amount of Si is also regulated, generally around 0.05% Si and 0.10% Fe.
We have obtained a material with a conductivity of 61.0% or more. Problems to be Solved by the Invention As mentioned above, it is possible to obtain an aluminum alloy with high conductivity by reducing the content of impurity elements such as Cu, Mn, Ti, and V as well as the content of Fe and Si as much as possible. If you try to reduce these amounts blindly, even if the conductivity increases, you will end up increasing the cost due to problems such as the cost of the metal and the melting furnace. This invention was made against the background of the above circumstances, and aims to provide an aluminum alloy that can reliably obtain high electrical conductivity of 61% or more without unnecessarily increasing costs. It is something. Means for Solving the Problems The inventors of the present invention have repeatedly studied in detail the relationship between electrical conductivity and the composition and structure of aluminum alloys, and found that instead of simply reducing the amount of impurities,
The inventors have discovered that a high conductivity material with a conductivity of 61% or more can be obtained by controlling the amount of Fe solid solution and the amount of Si solid solution in the alloy to below specific values, respectively, leading to the creation of this invention. That is, the conductive aluminum alloy of the present invention contains 0.04 to 0.70 wt% of Fe and 0.04 to 0.25 wt% of Si, and limits unavoidable impurities to 0.02 wt% or less for each element and 0.05 wt% or less in total. , the remainder is Al, and the solid solution amount of Fe is
The amount of solid solution of Si is 400 ppm or less. Effect The electrical conductivity of an aluminum alloy with a small content of impurity elements depends on the amount of Fe dissolved in the matrix (solid solution Fe amount) and the amount of Si dissolved in the matrix (solid solution amount). The amount of solute Si has a large influence, and the amount of solute Fe has a particularly large effect. solid solution
When compared with the same amount of solid solution, Si does not have as great an effect on conductivity as solid solution Fe, but Si has a higher solid solubility than Fe, and Si dissolved in solid solution in actual alloys is Since the amount of Si in solid solution is much larger than the amount of Fe in solid solution, quantitative fluctuations are large, and therefore the amount of Si in solid solution ultimately has a large effect on conductivity. The inventors investigated the effects of the amount of solid solute Fe and Si on conductivity, and found that even if the total amount of Fe, total Si, and other impurities in the alloy are regulated to a considerable extent, The amount of solid solute Fe is
It has been found that if the amount of Si in solid solution exceeds 100 ppm or the amount of solid solution Si exceeds 400 ppm, it is difficult to stably obtain a material with a conductivity of 61% or more. And conversely Fe
Even if the total amount of Si and the total amount of Si are large to some extent, solid solution
Fe content is 100ppm or less and solid solution Si content is 400ppm
It has been found that a material with a conductivity of 61% or more can be stably obtained if the following conditions are used. Therefore, in this invention, the amount of solid solution Fe is 100 ppm or less, and the amount of solid solution Si is
It was decided to limit the amount to 400ppm or less. Further, in the aluminum alloy of the present invention, the total amount of Fe, the total amount of Si, and the amount of unavoidable impurity elements are also specified, and the reasons for these limitations will be explained below. Fe: Setting the amount of Fe to less than 0.04% causes a significant increase in cost. Furthermore, if the amount of Fe exceeds 0.7%, depending on the casting method, the amount of forced solid solution of Fe will be significantly large.
It becomes difficult to regulate the amount of solid solution Fe to 100 ppm or less. Therefore, the total amount of Fe was set within the range of 0.04 to 0.7%. Si: Setting the amount of Si to less than 0.04% causes a significant cost increase, as in the case of Fe. On the other hand, if the amount of Si exceeds 0.25%, it becomes difficult to suppress the amount of solid solution Si to 400 ppm or less. Therefore, the total amount of Si is 0.04 ~
It was set within the range of 0.25%. Unavoidable impurities: In ordinary aluminum alloys, Mn,
Ti, Cr, V, Zr, Mg, Cu, etc. are included as unavoidable impurities, but if the individual content of any impurity element exceeds 0.02% or the total content exceeds 0.05%, the above-mentioned Even if the amount of solid solution Fe and the amount of solid solution Si are regulated to 100 ppm or less and 400 ppm or less, respectively, it will be difficult to obtain a conductivity of 61% or more. Therefore, unavoidable impurity elements are regulated to 0.02% or less for each, and 0.05% or less in total. Among various unavoidable impurity elements, especially Mn,
Ti, Cr, V, and Zr have a negative effect on conductivity, so
It is desirable that each of these be 0.01% or less. As described above, in the aluminum alloy of the present invention, the amount of solute Fe is 100 ppm or less, and the amount of solute Si is less than 100 ppm.
By regulating the content of unavoidable impurity elements to 400ppm or less, and regulating the content of unavoidable impurity elements as described above,
It has become possible to stably obtain materials with electrical conductivity of 61% or higher. Specific explanation for carrying out the invention Basically, the aluminum alloy of the present invention has a solid solute Fe amount and a solid solute Si amount of 100 ppm or less, respectively.
It is important that it is regulated to 400ppm or less,
The amount of solid solute Fe can be determined by the analysis method shown in Figure 1, and the amount of solid solution Si can be determined by the amount of residual Si determined by the analysis method shown in Figure 2. It can be obtained by subtracting it from the total amount of Si. Next, a method for manufacturing the conductive aluminum alloy of the present invention will be explained. As mentioned above, in the conductive aluminum alloy of this invention, the amount of solid solution Fe and Si in the alloy is regulated, and therefore, the manufacturing method also requires measures to control the amount of solid solution. It is necessary to take measures. Therefore, basically, prior to hot rolling, an alloy ingot with the above-mentioned composition is heated at 300 to 550℃ for 0.5 to 24 hours, and after hot rolling, the processing rate is
After 50% or more cold working (cold rolling or wire drawing, etc.), final annealing is performed at 220 to 330°C.
It is desirable to apply a method of heating for 0.5 to 24 hours. Alternatively, prior to hot rolling an alloy ingot having the above composition, heat it at 300 to 550°C for 0.5 to 24 hours in the same manner as described above, and after hot rolling, the processing rate is 30.
% or more and intermediate annealing for 0.5 to 24 hours at 220 to 330°C are repeated once or twice, and then final cold working is performed to a processing rate of 50% or more,
Thereafter, as final annealing, it is desirable to apply a method of heating at 220 to 330° C. for 0.5 to 24 hours in the same manner as described above. These manufacturing methods will be explained in more detail below. First, as mentioned above, Fe0.04~0.70%, Si0.04~
A molten aluminum alloy containing 0.25% and other unavoidable impurities of 0.02% or less for each element and 0.05% or less in total is cast in a conventional manner to create an ingot. Here, conventional methods include continuous casting using the Properch method, continuous casting and rolling method, etc.
It also means DC casting of billets and slabs. In such an ingot, the amount of solid solution of Fe is at least
It exceeds 300 ppm, and most of the added amount of Si is in solid solution. Naturally, conductivity is low at such a level of Fe and Si solid solution amounts, so the solid solution Fe and Si are precipitated in the post-casting process to reduce these solid solution amounts. It is necessary to do so. The first step for this purpose is heating and hot rolling of the ingot. In other words, the ingot is heated in the temperature range of 300 to 550℃ prior to hot rolling.
This is carried out under conditions of holding for 0.5 to 24 hours, and then hot rolling is carried out. However, this heating may be performed as a soaking treatment or as a heat treatment immediately before hot rolling. In other words, the ingot is 300 ~
After soaking at 550°C for 0.5 to 24 hours, the ingot may be reheated to that temperature range and subjected to hot rolling, or the ingot may be heated at 300 to 550°C for 0.5 to 24 hours and then rolled as is. It may also be subjected to hot rolling. As mentioned above, heat before hot rolling to 300~550℃
The reason for setting the time to 0.5 to 24 hours is as follows. In other words, since the precipitation of Fe is maximum in the range of 300 to 550℃, heating in that temperature range
The amount of solid solution of Fe can be reduced. 300 here
If the temperature is below 550°C, precipitation of Fe will be insufficient and the amount of solid solution cannot be reduced sufficiently, while if it exceeds 550°C, Fe will be re-dissolved and the amount of solid solution will increase. In addition, although Si does not precipitate as metallic Si at the ingot stage, solid solution Si migrates into Al-Fe crystals by heating at a temperature within the range of 300 to 550°C, resulting in αAlFeSi, βAlFeSi, and Al 3 Fe
(Si), and the precipitates also become αAlFeSi, etc., so that Fe precipitation and Si precipitation coexist. Here, below 300℃, the precipitation of Si is insufficient;
If the temperature exceeds 550°C, Si in the crystallized material will migrate back into the matrix, and the amount of Si solid solution in the matrix will increase. Note that if the ingot heating time is less than 0.5 hours, the effect of precipitating Fe and Si will not be sufficiently obtained.
On the other hand, heating for a long time exceeding 24 hours only unnecessarily increases costs. Therefore, the ingot heating conditions are 300-550°C for 0.5-24 hours. Of course, it is difficult to reduce the amount of solid solute Fe and Si to the target level only through the steps of ingot heating and hot rolling as described above, but the above conditions must be met before the subsequent treatment. By heat treatment at
Unless the solid solution levels of Fe and Si are lowered to appropriate levels, it will be difficult to lower them to the final target level. After hot rolling, cold working such as cold rolling and cold drawing is performed, and then final annealing is performed. In this case, the cold working is performed at a processing rate of 50% or more, and the final annealing is performed at 220 to 330°C. Heat for 0.5 to 24 hours at a temperature within the range of . These cold rolling and final annealing conditions are also important for promoting the precipitation of Fe and Si and reducing the amount of solid solution thereof. In other words, dislocations are important as precipitation sites for Fe and Si;
Increasing the dislocation density contributes to the precipitation of Fe and Si. Therefore, by increasing the degree of cold working and increasing the dislocation density, Fe,
It is possible to increase the amount of Si precipitated and reduce the amount of solid solution Fe and the amount of solid solution Si to the target level. In the final annealing after cold working, Fe and Si precipitate as AlFeSi precipitates, and Si also precipitates as metal Si. Here, if the cold working rate is less than 50%, the increase in dislocation density is insufficient, and the subsequent final annealing is sufficient.
Precipitation of Fe and Si cannot be planned. Also, the final annealing temperature is
Below 220℃, precipitation of Fe and Si is insufficient,
In particular, the precipitation of Fe becomes insufficient, and on the other hand, even if the temperature exceeds 330°C, the precipitation of Fe and Si is insufficient, and in particular, Si begins to dissolve into solid solution again, making it impossible to achieve a reduction in the amount of solid solution. If the final annealing time is less than 0.5 hours, Fe as described above,
Si is not sufficiently precipitated, and on the other hand, heating for a long time exceeding 24 hours only unnecessarily increases costs. Therefore, the processing rate of cold working is
50% or more, final annealing conditions are 220~330℃ x 0.5~
It was set as 24 hours. Note that the heating rate in the final annealing is preferably slow, and it is usually desirable to set the temperature increase rate to 100° C./hr or less. In addition, in order to further promote the precipitation of Fe and Si, primary cold working and intermediate annealing are performed once after hot rolling.
After doing this twice or repeating these two or more times,
Final cold working may be performed, followed by final annealing. In this case, it is preferable that the primary cold working is performed at a working rate of 30% or more, and the intermediate annealing is performed at 220 to 330°C for 0.5 to 24 hours. In this case as well, the final cold working is at least 50% as in the previous case, and the final annealing is also at 220~220%.
The temperature may be set at 330°C for 0.5 to 24 hours. By repeating the increase in dislocation rate through cold working and the precipitation of Fe and Si through annealing in the above temperature range,
It becomes possible to sufficiently reduce the amount of solid solution of Fe and Si. Example An alloy having the composition shown in alloy codes 1 and 2 in Table 1 was cast into a slab with a thickness of 500 mm and a width of 1200 mm using the DC casting method, and the slab was heated under the ingot heating conditions shown in Table 2. Then, it was hot-rolled according to a conventional method to obtain a hot-rolled sheet with a thickness of 4 mm. Then, the hot-rolled plate is
Cold rolling-final annealing or 1 as shown in the table
The treatment was performed according to the steps of next cold rolling - intermediate annealing - final cold rolling - final annealing. The amount of Fe solid solution and the amount of Si solid solution in the plate after final annealing was investigated using the method described above, and the electrical conductivity was also investigated. The results are also shown in Table 2.
【表】【table】
【表】
第2表において、条件符号A〜Cは同じ成分組
成の合金1について製造条件を変えることによつ
てFe固溶量、Si固溶量を異ならしめたものであ
るが、条件符号CではFe固溶量、Si固溶量がこ
の発明で規定する上限を越えているため61%以上
の導電率が得られなかつたのに対し、条件符号
A,BではFe固溶量、Si固溶量がそれぞれこの
発明の上限値の100ppm、400ppmを下廻り、導電
率61%以上を確保することができた。また条件符
号D,Eは合金2について製造条件を変えること
によりFe、Siの固溶量を異ならしめたものであ
り、この場合も条件符号EではFe固溶量、Si固
溶量がこの発明の上限を越えているため導電率が
低く、一方条件符号DではFe固溶量、Si固溶量
がそれぞれ100ppm、400ppmを下廻り、61%以上
の導電率を確保することができた。
発明の効果
この発明の導電用アルミニウム合金は、Feの
固溶量を100ppm以下に規制するとともにSiの固
溶量を400ppm以下に規制することによつて、Fe
の総含有量やSiの総含有量は極端に低減しなくて
も、またその他の不純物元素含有量を極端に規制
しなくても、61%以上の高導電率が確実に得ら
れ、したがつてこの発明の導電用アルミニウム合
金を用いれば、いたずらに高コスト化を招くこと
なく高導電率材料を得ることができる。[Table] In Table 2, condition codes A to C are those in which the amount of solid solution of Fe and the amount of solid solution of Si were made different by changing the manufacturing conditions for Alloy 1 with the same component composition, but condition code C In contrast, in condition codes A and B, the amount of Fe solid solution and the amount of Si solid solution were The dissolved amounts were below the upper limits of this invention, 100 ppm and 400 ppm, respectively, and a conductivity of 61% or more could be secured. Furthermore, condition codes D and E are obtained by changing the manufacturing conditions for Alloy 2 to make the solid solution amounts of Fe and Si different; in this case as well, in condition code E, the solid solution amounts of Fe and Si are the same as those of the present invention. On the other hand, in condition code D, the amount of Fe solid solution and the amount of Si solid solution were below 100 ppm and 400 ppm, respectively, and a conductivity of 61% or more could be secured. Effects of the Invention The conductive aluminum alloy of the present invention has the ability to reduce Fe by regulating the solid solution amount of Fe to 100 ppm or less and by regulating the solid solution amount of Si to 400 ppm or less.
A high conductivity of 61% or more can be reliably obtained without drastically reducing the total Si content or the total content of other impurity elements. Therefore, by using the conductive aluminum alloy of the present invention, a material with high conductivity can be obtained without unnecessarily increasing costs.
第1図はアルミニウム合金中におけるFeの固
溶量を測定するための分析方法を示すフローチヤ
ート、第2図はアルミニウム合金中における固溶
Siを除いた残渣Si量を測定するための分析方法を
示すフローチヤートである。
Figure 1 is a flowchart showing the analytical method for measuring the amount of solid solution of Fe in aluminum alloy, and Figure 2 is a flow chart showing the amount of solid solution of Fe in aluminum alloy.
This is a flowchart showing an analysis method for measuring the amount of residual Si after removing Si.
Claims (1)
し、不可避的不純物を各元素それぞれ0.02wt%以
下、総量で0.05wt%以下に規制し、残部がAlか
らなる成分組成を有し、しかもFeの固溶量が
100ppm以下、Siの固溶量が400ppm以下であるこ
とを特徴とする導電用アルミニウム合金。1 Contains 0.04 to 0.70 wt% of Fe, 0.04 to 0.25 wt% of Si, controls unavoidable impurities to 0.02 wt% or less for each element, and 0.05 wt% or less in total, and the remainder is Al. Moreover, the solid solution amount of Fe is
An aluminum alloy for conductive use, characterized by having a solid solution amount of Si of 400 ppm or less.
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP8367488A JPH01255637A (en) | 1988-04-05 | 1988-04-05 | Aluminum alloy for conducting electricity |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP8367488A JPH01255637A (en) | 1988-04-05 | 1988-04-05 | Aluminum alloy for conducting electricity |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| JPH01255637A JPH01255637A (en) | 1989-10-12 |
| JPH0543774B2 true JPH0543774B2 (en) | 1993-07-02 |
Family
ID=13809031
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP8367488A Granted JPH01255637A (en) | 1988-04-05 | 1988-04-05 | Aluminum alloy for conducting electricity |
Country Status (1)
| Country | Link |
|---|---|
| JP (1) | JPH01255637A (en) |
Families Citing this family (4)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JPH0621310B2 (en) * | 1990-06-26 | 1994-03-23 | 住友軽金属工業株式会社 | Highly conductive Al-Mg-Si alloy tube manufacturing method |
| JP5558639B1 (en) * | 2012-10-11 | 2014-07-23 | 株式会社Uacj | Bus bar plate conductor and bus bar comprising the same |
| JP6396067B2 (en) | 2014-04-10 | 2018-09-26 | 株式会社Uacj | Aluminum alloy plate for bus bar and manufacturing method thereof |
| JPWO2025028381A1 (en) * | 2023-07-31 | 2025-02-06 |
Family Cites Families (6)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| BE791269R (en) * | 1971-11-11 | 1973-03-01 | Southwire Co | ALUMINUM ALLOY TREFILE PRODUCTS AND PROCESS FOR THE |
| JPS495808A (en) * | 1972-05-11 | 1974-01-19 | ||
| JPS5211147B2 (en) * | 1972-05-30 | 1977-03-29 | ||
| FR2289035A1 (en) * | 1974-08-29 | 1976-05-21 | Trefimetaux | ELECTRICAL CONDUCTORS IN ALUMINUM ALLOYS AND PROCESS FOR OBTAINING |
| DE2742149A1 (en) * | 1976-09-22 | 1978-03-23 | Alusuisse | METHOD OF MANUFACTURING ELECTRIC CONDUCTOR WIRE |
| JPS549111A (en) * | 1977-06-23 | 1979-01-23 | Mitsubishi Keikinzoku Kogyo | Method of making conductive aluminum alloy wire |
-
1988
- 1988-04-05 JP JP8367488A patent/JPH01255637A/en active Granted
Also Published As
| Publication number | Publication date |
|---|---|
| JPH01255637A (en) | 1989-10-12 |
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