JPH09143604A - Aluminium-magnesium-silicon base alloy excellent in extrudability - Google Patents
Aluminium-magnesium-silicon base alloy excellent in extrudabilityInfo
- Publication number
- JPH09143604A JPH09143604A JP30432995A JP30432995A JPH09143604A JP H09143604 A JPH09143604 A JP H09143604A JP 30432995 A JP30432995 A JP 30432995A JP 30432995 A JP30432995 A JP 30432995A JP H09143604 A JPH09143604 A JP H09143604A
- Authority
- JP
- Japan
- Prior art keywords
- alloy
- particles
- billet
- extrudability
- content
- 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
Links
Landscapes
- Extrusion Of Metal (AREA)
Abstract
Description
【0001】[0001]
【発明の属する技術分野】この発明は、アルミサッシな
どの一般建材、その他構造材に用いられる押出性に優れ
たAl−Mg−Si系合金に関する。BACKGROUND OF THE INVENTION 1. Field of the Invention The present invention relates to an Al-Mg-Si alloy having excellent extrudability, which is used for general building materials such as aluminum sashes and other structural materials.
【0002】[0002]
【従来の技術】従来より、Al−Mg−Si系合金(J
IS6000系合金)は押出性に優れているため生産性
が高く、アルミサッシなどの一般建材やその他の構造材
に広く用いられている。また、最近では前記6000系
合金の押出加工における押出速度を速め、生産性を更に
向上させる試みがなされている。2. Description of the Related Art Al-Mg-Si alloys (J
(IS6000 series alloy) has high productivity because it has excellent extrudability, and is widely used for general building materials such as aluminum sashes and other structural materials. Further, recently, attempts have been made to increase the extrusion speed in the extrusion processing of the 6000 series alloy to further improve the productivity.
【0003】しかし、押出速度を速めると6000系合
金のビレット中に含有される不溶性のAl−Fe−Si
粒子が起源となって押出材にむしれやピックアップ等の
表面欠損が発生するため、表面品質を維持しつつ生産性
を向上させるためには、Al−Fe−Si粒子の含有量
などの制御が重要な課題の一つとなっていた。However, when the extrusion speed is increased, the insoluble Al-Fe-Si contained in the billet of the 6000 series alloy.
Particles are the origin and peeling and surface defects such as pickup occur in the extruded material. Therefore, in order to improve the productivity while maintaining the surface quality, it is necessary to control the content of Al-Fe-Si particles and the like. It was one of the important issues.
【0004】そこで、6000系合金に微量のMnを添
加し、該合金を高温で均熱処理することにより、表面欠
損の起源となるAl−Fe−Si粒子を微細化し、ビレ
ット全体に渡って該粒子を均等に分散させることで、押
出速度を速めても表面欠損の発生を抑えることのできる
合金が特公平4−72899号公報により報告されてい
る。Therefore, a small amount of Mn is added to the 6000 series alloy, and the alloy is subjected to a soaking treatment at a high temperature to make Al-Fe-Si particles, which are the origin of surface defects, finer, and the particles are spread over the entire billet. Japanese Patent Publication No. 4-72899 reports an alloy capable of suppressing the occurrence of surface defects even if the extrusion speed is increased by evenly dispersing the alloy.
【0005】[0005]
【発明が解決しようとする課題】ところが、6000系
合金にMnを添加してAl−Fe−Si粒子を微細化さ
せた場合には、鋳造により得られた該合金のビレットを
均熱処理する工程において、585℃前後の高い温度で
数時間の加熱を必要としていた。従って、上記の合金は
押出加工における生産性は向上するものの、多量のエネ
ルギーを必要としコストの上昇を招くものであった。However, when Mn is added to a 6000 series alloy to make Al-Fe-Si particles finer, in the step of soaking the billet of the alloy obtained by casting in a soaking process. Heating at a high temperature around 585 ° C for several hours was required. Therefore, although the above-mentioned alloy improves productivity in extrusion processing, it requires a large amount of energy and causes an increase in cost.
【0006】この発明は、上記問題に鑑みてなされたも
のであり、押出加工における押出速度を速めて高生産性
を確保しつつ、表面品質を維持することができ、かつ、
Al−Fe−Si粒子を微細化し均質化するための均熱
処理に関して省エネルギーを実現できるAl−Mg−S
i系合金の提供を目的とする。The present invention has been made in view of the above problems, and it is possible to maintain the surface quality while increasing the extrusion speed in the extrusion process to ensure high productivity, and
Al-Mg-S that can realize energy saving for soaking for finely homogenizing Al-Fe-Si particles
The purpose is to provide an i-based alloy.
【0007】[0007]
【課題を解決するための手段】この発明者は、鋭意研究
と実験の結果、押出性に優れたAl−Mg−Si系合金
をベースとして、これに所定量のNiを含有せしめるこ
とにより上記目的を達成し得ることを見出だし、この発
明をするに至った。As a result of earnest research and experimentation, the present inventor has found that the above object is obtained by adding a predetermined amount of Ni to an Al-Mg-Si-based alloy having excellent extrudability as a base. The inventors have found that the above can be achieved, and have reached the present invention.
【0008】即ち、この発明は、Mg:0.35〜0.
80wt%、Si:0.20〜0.90wt%、Fe:0.
16〜0.25wt%、Ni:0.01〜0.15wt%、
Cu:0.01〜0.20wt%、Ti:0.01〜0.
02wt%を含有し、残部がアルミニウム及び不純物から
なることを特徴とする押出性に優れたAl−Mg−Si
系合金を要旨とするものである。また、上記元素に加え
て任意的にMn:0.15wt%以下、Cr:0.10wt
%以下のいずれか1種または2種を含有しても良い。That is, according to the present invention, Mg: 0.35 to 0.
80 wt%, Si: 0.20 to 0.90 wt%, Fe: 0.
16 to 0.25 wt%, Ni: 0.01 to 0.15 wt%,
Cu: 0.01-0.20 wt%, Ti: 0.01-0.
Al-Mg-Si excellent in extrudability characterized by containing 02 wt% and the balance being aluminum and impurities
It is based on a system alloy. In addition to the above elements, Mn: 0.15 wt% or less, Cr: 0.10 wt%
You may contain any 1 type or 2 types of% or less.
【0009】上記において、Mg、Siは合金の強度向
上に寄与する元素である。しかし、Mgが0.35wt%
未満、Siが0.20wt%未満の含有率ではその効果に
乏しく、逆にMgが0.80wt%を越え、Siが0.9
0wt%を越える含有率の場合押出性が低下する。従っ
て、Mgは0.35〜0.80wt%、Siは0.20〜
0.90wt%の範囲で含有しなければならない。特に好
ましい含有率の下限値は、Mg:0.40wt%、Si:
0.35wt%であり、上限値はMg:0.75wt%、S
i:0.85wt%である。In the above, Mg and Si are elements that contribute to improving the strength of the alloy. However, Mg is 0.35 wt%
%, Si is less than 0.20 wt%, the effect is poor, conversely Mg exceeds 0.80 wt%, Si is 0.9
If the content exceeds 0 wt%, the extrudability will decrease. Therefore, Mg is 0.35-0.80 wt% and Si is 0.20-
It must be contained in the range of 0.90 wt%. Particularly preferred lower limits of the content are Mg: 0.40 wt% and Si:
0.35 wt%, the upper limit is Mg: 0.75 wt%, S
i: 0.85 wt%
【0010】Feは、合金の中にあって押出成形時の表
面欠損発生の原因となる不溶性のAl−Fe−Si粒子
を形成するため、その含有を極力抑えるのが好ましい
が、Feの含有率が低くなるほど合金自体の価格が高く
なり、また、成形後に行うことのある陽極酸化による表
面の色彩が不均一になるため、Feの含有率の下限値は
0.16wt%に制限される。[0010] Fe forms insoluble Al-Fe-Si particles in the alloy that cause surface defects during extrusion molding, so it is preferable to suppress the content of Fe as much as possible. The lower the value, the higher the price of the alloy itself, and the more uneven the surface color due to anodic oxidation that may be performed after forming. Therefore, the lower limit of the Fe content is limited to 0.16 wt%.
【0011】一方、合金中にAl−Fe−Si粒子が含
まれる場合には、その粒子径が微細であり、合金に均一
に分布し、かつ、α化率が高いほど表面欠損の発生する
確率は低くなる。この発明は、6000系合金にNiを
添加してAl−Fe−Si粒子の微細化及びα化を促進
するものであるが、Feの含有率が高ければ、Niの添
加によってもAl−Fe−Si粒子の微細化及びα化を
促進しきれなくなるため、Feの含有率の上限値は0.
25wt%に制限される。On the other hand, when Al-Fe-Si particles are contained in the alloy, the particle size is fine, the particles are evenly distributed in the alloy, and the higher the α-conversion rate, the higher the probability of occurrence of surface defects. Will be lower. In the present invention, Ni is added to the 6000 series alloy to promote the refinement and alpha conversion of the Al-Fe-Si particles. However, if the Fe content is high, the addition of Ni also causes Al-Fe- The upper limit of the Fe content is 0.
Limited to 25 wt%.
【0012】従って、Feは0.16〜0.25wt%の
範囲で含有しなければならない。特に好ましいFeの含
有率の下限値は、0.18wt%、上限値は0.22wt%
である。Therefore, Fe must be contained in the range of 0.16 to 0.25 wt%. Particularly preferable Fe content is 0.18 wt% as the lower limit and 0.22 wt% as the upper limit.
It is.
【0013】Niは、その添加によって不溶性のAl−
Fe−Si粒子のα化及び微細化を促進する元素であ
る。よって、Niの含有率が0.01wt%未満であれば
α化及び微細化促進効果に乏しくなる。一方0.15wt
%を越えて含有すれば前記効果が飽和するばかりでなく
合金の耐食性が低下する。従ってNiは0.01〜0.
15wt%の範囲で含有しなければならない。特に好まし
いNiの含有率の下限値は、0.03wt%、上限値は、
0.10wt%である。Ni is insoluble in Al-
It is an element that promotes α-formation and miniaturization of Fe-Si particles. Therefore, if the Ni content is less than 0.01 wt%, the effect of promoting α-formation and refinement becomes poor. On the other hand, 0.15 wt
If it is contained in excess of%, not only the above effect is saturated but also the corrosion resistance of the alloy is lowered. Therefore, Ni is 0.01-0.
It must be contained in the range of 15 wt%. A particularly preferable lower limit of the Ni content is 0.03 wt% and an upper limit thereof is
It is 0.10 wt%.
【0014】Cuは合金の強度向上に寄与するものであ
るが、その含有率が0.01wt%未満ではその効果に乏
しく、0.20wt%を越えれば効果が飽和する。また、
Tiは結晶粒の微細化に寄与し、その含有率が0.01
wt%未満ではその効果に乏しく、0.02wt%を越えれ
ば効果が飽和する。Cu contributes to improving the strength of the alloy, but if its content is less than 0.01 wt%, its effect is poor, and if it exceeds 0.20 wt%, the effect is saturated. Also,
Ti contributes to the refinement of crystal grains, and its content is 0.01
If it is less than wt%, the effect is poor, and if it exceeds 0.02 wt%, the effect is saturated.
【0015】任意的に添加されるMnはNiと同じくA
l−Fe−Si粒子の微細化に寄与するものであるが、
0.15wt%を越えて添加しても微細化効果が飽和す
る。また、Crは結晶粒を微細化して合金の強度向上に
寄与するものであるが、0.10wt%を越えて添加して
も微細化効果が飽和し、さらなる添加は経済的な無駄を
発生する。Mn、Crの1種または2種を含有する場合
の特に好ましい含有率の下限値はMn:0.02wt%、
Cr:0.01wt%であり、上限値はMn:0.12wt
%、Cr:0.10wt%である。Mn, which is optionally added, has the same A content as Ni.
Although it contributes to miniaturization of 1-Fe-Si particles,
Even if added over 0.15 wt%, the miniaturization effect is saturated. Further, Cr contributes to improving the strength of the alloy by refining the crystal grains, but even if added in excess of 0.10 wt%, the refining effect is saturated and further addition causes economical waste. . Particularly preferred lower limit of the content of Mn and Cr containing Mn and Cr is 0.02 wt%,
Cr: 0.01 wt%, the upper limit is Mn: 0.12 wt
%, Cr: 0.10 wt%.
【0016】なお、押出成形後に行う時効処理の効率の
向上を目的として、この発明に係る合金にBe元素を添
加しても良い。具体的にはBeの含有率を0.0005
〜0.15wt%の範囲となるように添加するのが好まし
く、特に好ましいBeの含有率の下限値は0.001wt
%であり、上限値は0.10wt%である。The Be element may be added to the alloy according to the present invention for the purpose of improving the efficiency of the aging treatment performed after extrusion molding. Specifically, the Be content is 0.0005.
It is preferable to add it in the range of 0.15 wt%, and the particularly preferable lower limit of the Be content is 0.001 wt%.
%, And the upper limit is 0.10 wt%.
【0017】この発明に係る合金を製造するにあたって
は、各元素を上記の含有率の範囲になるよう常法に従っ
て調整溶解した後、所定形状のビレットに鋳造する。次
に、該ビレットを均質化させ、合金中に含まれるAl−
Fe−Si粒子を微細化、α化させて合金中に均等に分
散させるために均熱処理を施す。該均熱処理の温度条件
等は任意に選択し得るが、この発明ではNiを添加する
ことによってAl−Fe−Si粒子の微細化、α化を比
較的低温の均熱処理で実現することができるため、時間
的及びエネルギー的コストを勘案し、550〜570℃
の温度で1.5〜3時間の範囲で均熱処理をするのが良
い。In producing the alloy according to the present invention, each element is adjusted and melted according to a conventional method so as to be in the above content range, and then cast into a billet having a predetermined shape. Next, the billet is homogenized, and Al- contained in the alloy is
A soaking process is performed in order to make the Fe-Si particles finer, to be α, and to disperse them uniformly in the alloy. Although the temperature condition of the soaking can be arbitrarily selected, in the present invention, by adding Ni, the Al—Fe—Si particles can be made finer and can be made α by a soaking at a relatively low temperature. , 550 to 570 ℃ in consideration of time and energy cost
It is preferable to perform soaking at a temperature of 1.5 to 3 hours.
【0018】[0018]
【実施例】次に、この発明の実施例を示す。Next, an embodiment of the present invention will be described.
【0019】表1に示すように、実施例として、この発
明の組成範囲内にある6種類の試料A〜Fと、比較例と
して、組成範囲外にある3種類の試料G〜Iを作成し
た。前記各試料は、常法に従い各組成物を調製し溶解し
た後、鋳造により所定の形状のビレットに成形した。な
お、この実施例で使用したビレットの形状は直径6イン
チ×長さ650mmである。As shown in Table 1, six types of samples A to F within the composition range of the present invention and three types of samples G to I out of the composition range were prepared as comparative examples. . Each of the above-mentioned samples was formed into a billet having a predetermined shape by casting, after preparing and dissolving each composition according to a conventional method. The billet used in this example had a diameter of 6 inches and a length of 650 mm.
【0020】[0020]
【表1】 [Table 1]
【0021】次に、Al−Fe−Si粒子を微細化、α
化してビレット中に均等に分散させるために均熱処理を
施した。該均熱処理の条件は、比較例との有意差を確認
するために下記表2に示す各種に設定した。Next, the Al--Fe--Si particles are refined and α
A soaking process was carried out in order to form and uniformly disperse in the billet. The conditions of the soaking treatment were set to various values shown in Table 2 below in order to confirm a significant difference from the comparative example.
【0022】[0022]
【表2】 [Table 2]
【0023】なお、上記均熱処理後、一旦ビレットを冷
却するが、該ビレットの冷却方法には特に制限はない。After the soaking treatment, the billet is once cooled, but the method for cooling the billet is not particularly limited.
【0024】次に、上記各条件で均熱処理したビレット
を常法に従って押出加工を行った。この実施例は、直接
押出法を採用し、470℃に加熱したビレットを、高さ
47mm,幅29mmの押出形材に押し出した。押出速
度は40m/minに設定した。Next, the billet subjected to the soaking treatment under the above respective conditions was extruded according to a conventional method. In this example, the direct extrusion method was adopted, and the billet heated to 470 ° C. was extruded into an extruded profile having a height of 47 mm and a width of 29 mm. The extrusion speed was set to 40 m / min.
【0025】次に、上記押出材につき200℃×3時間
の時効処理を行い、押出材の完成品を得た。Next, the extruded material was subjected to an aging treatment at 200 ° C. for 3 hours to obtain a finished extruded material.
【0026】こうして得られた押出材の表面を目視にて
観察し、各合金における押出材の表面品質を評価した。
この結果を下記表3に示す。なお、押出前のビレット中
に含まれるAl−Fe−Si粒子のα化率と押出後の表
面品質との相関を得るために、ビレットのα化率を測定
しており、該測定結果を下記表3に合わせて記す。The surface of the extruded material thus obtained was visually observed to evaluate the surface quality of the extruded material in each alloy.
The results are shown in Table 3 below. In order to obtain the correlation between the α-gelatinization rate of Al-Fe-Si particles contained in the billet before extrusion and the surface quality after extrusion, the α-gelatinization rate of the billet was measured. It writes according to Table 3.
【0027】[0027]
【表3】 [Table 3]
【0028】表3の結果からわかるように、この発明に
係る組成範囲のビレットは、均熱処理の温度、及び時間
に関わりなく、Al−Fe−Si粒子が完全にα化して
おり、押出後の押出材の表面は欠損が殆ど認められず、
比較例に比べて表面品質が良好であることを確認し得
た。As can be seen from the results in Table 3, in the billet having the composition range according to the present invention, the Al-Fe-Si particles were completely converted into α, regardless of the temperature and time of soaking, and the billet after extrusion was Almost no defects were observed on the surface of the extruded material,
It was confirmed that the surface quality was better than that of the comparative example.
【0029】[0029]
【発明の効果】この発明は、上述の次第で、6000系
の合金中に所定量のNiが含有されてなるものであるか
ら、550〜570℃という低い均熱温度でも、ビレッ
ト中のAl−Fe−Si粒子の微細化、α化が促進さ
れ、該ビレットの押出加工における押出速度を速めて
も、押出材に表面欠損が現れない。従って、この発明の
合金によれば表面品質を維持しつつ高い生産性を確保す
ることができ、なおかつ、省エネルギーを実現すること
ができる。According to the present invention, the 6000 series alloy contains a predetermined amount of Ni, depending on the above. Therefore, even if the soaking temperature as low as 550 to 570 ° C., the Al-- The Fe-Si particles are promoted to be finer and to be alpha, and surface defects do not appear in the extruded material even if the extrusion speed in the extrusion of the billet is increased. Therefore, according to the alloy of the present invention, high productivity can be secured while maintaining the surface quality, and energy saving can be realized.
Claims (2)
を特徴とする押出性に優れたAl−Mg−Si系合金。1. Mg: 0.35 to 0.80 wt% Si: 0.20 to 0.90 wt% Fe: 0.16 to 0.25 wt% Ni: 0.01 to 0.15 wt% Cu: 0.01 -0.20 wt% Ti: 0.01-0.02 wt%, the balance being aluminum and impurities, and an Al-Mg-Si based alloy excellent in extrudability.
ム及び不純物からなることを特徴とする押出性に優れた
Al−Mg−Si系合金。2. Mg: 0.35 to 0.80 wt% Si: 0.20 to 0.90 wt% Fe: 0.16 to 0.25 wt% Ni: 0.01 to 0.15 wt% Cu: 0.01 -0.20 wt% Ti: 0.01-0.02 wt%, Mn: 0.15 wt% or less Cr: 0.10 wt% or less Any one or two types are contained, and the balance is aluminum and An Al-Mg-Si based alloy excellent in extrudability characterized by comprising impurities.
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP30432995A JPH09143604A (en) | 1995-11-22 | 1995-11-22 | Aluminium-magnesium-silicon base alloy excellent in extrudability |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP30432995A JPH09143604A (en) | 1995-11-22 | 1995-11-22 | Aluminium-magnesium-silicon base alloy excellent in extrudability |
Publications (1)
Publication Number | Publication Date |
---|---|
JPH09143604A true JPH09143604A (en) | 1997-06-03 |
Family
ID=17931706
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
JP30432995A Pending JPH09143604A (en) | 1995-11-22 | 1995-11-22 | Aluminium-magnesium-silicon base alloy excellent in extrudability |
Country Status (1)
Country | Link |
---|---|
JP (1) | JPH09143604A (en) |
Cited By (3)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
EP2072628A1 (en) * | 2007-12-19 | 2009-06-24 | Aleris Aluminum Bonn GmbH | High strength crash resistant aluminium alloy |
CN103966483A (en) * | 2014-04-10 | 2014-08-06 | 安徽银力铸造有限公司 | Anti-corrosion aluminum alloy sheet for automobiles |
JP2021085040A (en) * | 2019-11-25 | 2021-06-03 | 昭和電工株式会社 | Rolled aluminum alloy material having excellent thermal conductivity, electrical conductivity and strength and method for producing the same |
-
1995
- 1995-11-22 JP JP30432995A patent/JPH09143604A/en active Pending
Cited By (4)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
EP2072628A1 (en) * | 2007-12-19 | 2009-06-24 | Aleris Aluminum Bonn GmbH | High strength crash resistant aluminium alloy |
CN103966483A (en) * | 2014-04-10 | 2014-08-06 | 安徽银力铸造有限公司 | Anti-corrosion aluminum alloy sheet for automobiles |
CN103966483B (en) * | 2014-04-10 | 2016-03-23 | 安徽银力铸造有限公司 | A kind of corrosion-resistant automobile aluminum alloy sheet |
JP2021085040A (en) * | 2019-11-25 | 2021-06-03 | 昭和電工株式会社 | Rolled aluminum alloy material having excellent thermal conductivity, electrical conductivity and strength and method for producing the same |
Similar Documents
Publication | Publication Date | Title |
---|---|---|
CN110724859B (en) | Homogenized 6-series aluminum alloy and preparation method thereof | |
JPH0118979B2 (en) | ||
WO2017006490A1 (en) | Aluminum alloy extruded material having positive electrode oxide film and excellent external appearance quality and production method therefor | |
JPH07109536A (en) | Aluminum alloy for forging and heat treatment therefor | |
CN109136685B (en) | A kind of aluminium alloy and its preparation method and application | |
CN114480927A (en) | High-performance 6-series aluminum alloy | |
JP3767492B2 (en) | Method for producing aluminum flexible foil | |
CN113881877A (en) | Aluminum alloy strip and preparation method and application thereof | |
CN111041291B (en) | High-strength aluminum alloy material and preparation method thereof | |
WO2017006816A1 (en) | Aluminum alloy extruded material having positive electrode oxide film and excellent external appearance quality and production method therefor | |
CN114351019B (en) | Aluminum alloy material and preparation method and application thereof | |
JPH09143604A (en) | Aluminium-magnesium-silicon base alloy excellent in extrudability | |
JP3829164B2 (en) | Semi-melt molding material manufacturing method | |
JPS61259828A (en) | Production of high-strength aluminum alloy extrudate | |
JP3550944B2 (en) | Manufacturing method of high strength 6000 series aluminum alloy extruded material with excellent dimensional accuracy | |
JP4144184B2 (en) | Manufacturing method of heat-resistant Al alloy wire for electric conduction | |
JP3727041B2 (en) | Manufacturing method of Al-Mg-Si alloy extruded material for rotating parts and sliding parts with excellent surface roughness | |
JPS5826425B2 (en) | Manufacturing method for high-strength aluminum alloy with excellent mechanical properties in the thickness direction | |
JP2003164903A (en) | Method for manufacturing aluminium foil | |
CN111440973A (en) | Wrought aluminum alloy for improving hub cracking and processing method thereof | |
JPH0860283A (en) | Aluminum alloy sheet for di can body and its production | |
JPS627836A (en) | Manufacture of aluminum alloy having fine-grained structure | |
CN115652232B (en) | Processing technology for improving 6063 aluminum alloy anodic oxidation effect | |
JPS6158546B2 (en) | ||
JPS63243247A (en) | High-strength aluminum-based composite conductive wire and its production |