JPH06272001A - Production of al-mg-si series alloy metal plate excellent in heating hardenability - Google Patents

Production of al-mg-si series alloy metal plate excellent in heating hardenability

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Publication number
JPH06272001A
JPH06272001A JP8547993A JP8547993A JPH06272001A JP H06272001 A JPH06272001 A JP H06272001A JP 8547993 A JP8547993 A JP 8547993A JP 8547993 A JP8547993 A JP 8547993A JP H06272001 A JPH06272001 A JP H06272001A
Authority
JP
Japan
Prior art keywords
heating
less
rolling
hot rolling
temperature
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
Application number
JP8547993A
Other languages
Japanese (ja)
Other versions
JP2925884B2 (en
Inventor
Kunihiko Kishino
邦彦 岸野
Katsutoshi Sasaki
勝敏 佐々木
Hajime Watanabe
元 渡辺
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
JFE Steel Corp
Furukawa Aluminum Co Ltd
Original Assignee
Furukawa Aluminum Co Ltd
Kawasaki Steel Corp
Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)
Filing date
Publication date
Application filed by Furukawa Aluminum Co Ltd, Kawasaki Steel Corp filed Critical Furukawa Aluminum Co Ltd
Priority to JP8547993A priority Critical patent/JP2925884B2/en
Publication of JPH06272001A publication Critical patent/JPH06272001A/en
Application granted granted Critical
Publication of JP2925884B2 publication Critical patent/JP2925884B2/en
Anticipated expiration legal-status Critical
Expired - Fee Related legal-status Critical Current

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Abstract

PURPOSE:To produce an Al-Mg-Si series alloy metal plate excellent in heating hardenability by subjecting an Al allay contg. specified amounts of Mg, Si, Fe, Cu, Zn, Mn, Cr, Zr, Ti, B and Be to a specified homogenizing treatment, hot rolling, cold rolling and solution treatment. CONSTITUTION:The ingot of an Al alloy contg., by weight, 0.2 to 2% Mg and 0.2 to 2% Si and furthermore contg. one or more kinds among <=2% Fe, <=2% Cu, <=3% Zn, <=2% Mn, <=0.5% Cr, <=0.3% Zr, <=0.2% Ti, <=0.1% B and <=0.05% Be, and the balance substantial Al is heated to >=480 deg.C and is subjected to homogenizing treatment. After that, this ingot is heated to >=480 deg.C, is thereafter subjected to hot rolling and is passed through the temp. range of 360 to 450 deg.C for <15min, and it is completed at <=360 deg.C. Subsequently, this hot rolled plate is subjected to cold rolling including intermediate rolling according to necessary to regulate its plate thickness into a prescribed one. Next, this cold rolled plate is subjected to solution treatment of heating to >=500 deg.C for >=10sec.

Description

【発明の詳細な説明】Detailed Description of the Invention

【0001】[0001]

【産業上の利用分野】本発明は成形加工後に焼付け塗装
等の加熱が行われる部材用のAl−Mg−Si系合金板
材の製造方法に関するものであり、さらに詳しくは成形
後の加熱により強度増大が顕著な構造部品用のアルミニ
ウム合金板材が得られるものである。
BACKGROUND OF THE INVENTION 1. Field of the Invention The present invention relates to a method for producing an Al-Mg-Si alloy sheet for a member which is heated by baking after forming, and more specifically, the strength is increased by heating after forming. It is possible to obtain an aluminum alloy plate material for a structural part in which

【0002】[0002]

【従来の技術】現在自動車外板あるいはホイール用板材
等の部材としては板材を成形して所定の形状として使用
されている。このような部材に使用されるアルミニウム
板材への要求特性は、成形時に所定の形状に成形できる
ための高い成形性と、部材として使用する際に高い強度
や耐食性とを合わせ持つ信頼性を同時に満足させること
である。
2. Description of the Related Art At present, a plate material is molded and used as a member such as a vehicle outer plate or a wheel plate member. The characteristics required for aluminum plate materials used for such members are high moldability so that they can be formed into a predetermined shape at the time of molding and high reliability and high corrosion resistance when used as members at the same time. It is to let.

【0003】このような特性を合わせもつ材料としてA
l−Mg系合金とAl−Mg−Si系合金の板材が一般
的に使用されている。このAl−Mg系合金は中程度の
強度を有し、特に成形性において優れていることが特徴
であり、一方Al−Mg−Si系合金は成形性はAl−
Mg系合金に多少劣るものの、塗装加熱によって強度が
増大することが特徴である。それゆえ、複雑な形状の部
品にはAl−Mg系合金が、高強度を要求される部品に
はAl−Mg−Si系合金が使用される傾向にある。
As a material having such characteristics, A
Plate materials of 1-Mg-based alloy and Al-Mg-Si-based alloy are generally used. This Al-Mg-based alloy is characterized by having medium strength and particularly excellent formability, while the Al-Mg-Si-based alloy has a formability of Al-
Although somewhat inferior to Mg-based alloys, it is characterized in that the strength increases as the coating is heated. Therefore, there is a tendency that an Al-Mg-based alloy is used for parts having complicated shapes and an Al-Mg-Si-based alloy is used for parts requiring high strength.

【0004】[0004]

【発明が解決しようとする課題】近年自動車の燃費向
上、電気製品や機械製品の操作性、効率向上が強く要求
される傾向にあり、その為にそれら製品の部品に対して
軽量化要求がさらに強まりを見せている。そのような要
求を受けて部材の薄肉化が進み、素材であるアルミニウ
ム材料に対してもさらなる高強度化が要求されている。
In recent years, there has been a strong demand for improvement of fuel efficiency of automobiles, improvement of operability of electric products and mechanical products, and improvement of efficiency. Therefore, there is a further demand for weight reduction of parts of those products. It is showing strength. In response to such demands, the thickness of members has been reduced, and even higher strength is required for aluminum materials as raw materials.

【0005】そこでAl−Mg−Si系合金の加熱硬化
性をより高くする検討が精力的に行われている。しかし
一方では塗装工程の効率化の観点から加熱条件の低温・
短時間化が進む傾向にあり、Al−Mg−Si系合金が
硬化しにくい条件が採用される傾向となっている。この
ような背景にあって、より高い加熱硬化性を有する板材
の開発が強く望まれている。
Therefore, vigorous studies have been made to improve the heat-hardening property of Al-Mg-Si alloys. However, on the other hand, from the viewpoint of improving the efficiency of the painting process,
There is a tendency to shorten the time, and there is a tendency to adopt conditions under which the Al-Mg-Si alloy is hard to harden. Against this background, development of a plate material having higher heat-curing property is strongly desired.

【0006】[0006]

【課題を解決するための手段】本発明者らはこれらの問
題点を解決するため、Al−Mg−Si系合金板材中の
組織に着目して詳細に検討した結果本発明に至ったもの
であり、さらに詳しくは、Al−Mg−Si系合金板材
に高い加熱硬化性を付与する為の組織を熱間圧延工程の
制御により得ることに成功したものである。
Means for Solving the Problems In order to solve these problems, the present inventors have made a detailed study by paying attention to the structure in an Al—Mg—Si alloy plate material, and as a result, have arrived at the present invention. More specifically, the present invention succeeds in obtaining a structure for imparting a high heat-hardening property to an Al-Mg-Si alloy sheet material by controlling the hot rolling process.

【0007】即ち本発明のAl−Mg−Si系合金板材
の製造方法は、Mg: 0.2〜2wt%、Si: 0.2〜2wt
%を含み、かつFe:2wt%以下、Cu:2wt%以下、
Zn:3wt%以下、Mn:2wt%以下、Cr: 0.5wt%
以下、Zr: 0.3wt%以下、Ti: 0.2wt%以下、B:
0.1wt%以下、Be:0.05wt%の1種もしくは2種以上
を含有し、残部が実質的にAlからなるAl合金鋳塊を
480℃以上に加熱して均質化処理した後、又は均質化処
理後熱間圧延途中で 480℃以上に加熱した後、熱間圧延
において 360〜450 ℃の温度範囲を15分未満で通過させ
て熱間圧延終了温度を 360℃以下とし、その後冷間圧延
を行い、さらに必要に応じて冷間圧延途中で中間焼鈍を
施して所定板厚とした後、 500℃以上の温度に10秒以上
加熱する溶体化処理を施すことを特徴とするものであ
る。
That is, the manufacturing method of the Al-Mg-Si alloy sheet according to the present invention is as follows: Mg: 0.2-2 wt%, Si: 0.2-2 wt%
%, And Fe: 2 wt% or less, Cu: 2 wt% or less,
Zn: 3 wt% or less, Mn: 2 wt% or less, Cr: 0.5 wt%
Below, Zr: 0.3 wt% or less, Ti: 0.2 wt% or less, B:
An Al alloy ingot containing 0.1 wt% or less and Be: 0.05 wt% of 1 type or 2 types or more, and the balance substantially consisting of Al.
After heating to 480 ° C or higher for homogenization, or after heating to 480 ° C or higher during hot rolling after homogenization, pass the temperature range of 360 to 450 ° C in less than 15 minutes in hot rolling. The hot rolling finish temperature is set to 360 ° C or less, then cold rolling is performed, and if necessary, intermediate annealing is performed in the middle of cold rolling to obtain a predetermined plate thickness, and then heating to a temperature of 500 ° C or more for 10 seconds or more. It is characterized in that it is subjected to solution treatment.

【0008】[0008]

【作用】本発明において対象とするAl合金組成を上記
のように限定したのは、以下の理由による。即ちMg,
Siのいずれかが 0.2wt%未満では十分な加熱硬化性が
得られず、2wt%を越えて含有されると成形性が低下し
てしまう。
The reason for limiting the Al alloy composition targeted in the present invention as described above is as follows. That is, Mg,
If any of Si is less than 0.2 wt%, sufficient heat-curability cannot be obtained, and if more than 2 wt% is contained, the formability is deteriorated.

【0009】またFe,Cu,Zn,Mn,Cr,Z
r,Ti,B,Beの各元素は材料中に固溶あるいは微
細な化合物を生じて、材料組織の均質化と強度向上に寄
与するものであり、本Al合金にはこれらの1種もしく
は2種以上が添加される。しかしてそれぞれの上限を越
えて添加された場合は粗大な化合物を生じて成形性、強
度のいずれをも低下させる。
Fe, Cu, Zn, Mn, Cr, Z
Each element of r, Ti, B, and Be forms a solid solution or a fine compound in the material, and contributes to homogenization of the material structure and improvement of strength. More than one seed is added. However, if added in excess of the respective upper limits, a coarse compound is produced and moldability and strength are both reduced.

【0010】次に本発明の最大の特徴である熱間圧延条
件について説明する。本発明の製造方法が対象とするA
l−Mg−Si系合金において加熱硬化性を高める為に
は、溶体化処理時にMg,Si元素を可能な限り多く固
溶させる必要がある。そのための手段について発明者ら
はAl−Mg−Si系合金の組織挙動について詳細な検
討を重ねた。
Next, the hot rolling condition, which is the most characteristic feature of the present invention, will be described. A targeted by the production method of the present invention
In order to improve the heat-hardening property in the 1-Mg-Si based alloy, it is necessary to make Mg and Si elements in a solid solution as much as possible during the solution treatment. Regarding the means therefor, the inventors have made detailed studies on the structural behavior of the Al—Mg—Si alloy.

【0011】そして本発明の製造方法はその結果なされ
たものである。即ち溶体化処理時におけるMg,Si固
溶量を最大にするためには、溶体化処理前におけるM
g,Siの固溶度を可能な限り高めると共に、これら元
素を含む化合物のサイズを細かく分散する必要がある。
これら化合物は材料を高温で加熱する事により固溶反応
が進行し、材料中の化合物の体積率は減少し、固溶度が
増大する。従って材料を可能な限り高温に加熱すること
で、前述のMg,Siを含む化合物体積率の減少、固溶
量の増大が生じ、加熱硬化性を向上するのに有効であ
る。
The manufacturing method of the present invention has been made as a result. That is, in order to maximize the amount of solid solution of Mg and Si during solution treatment, M before solution treatment
It is necessary to increase the solid solubility of g and Si as much as possible and finely disperse the size of the compound containing these elements.
The solid solution reaction of these compounds proceeds by heating the material at a high temperature, the volume ratio of the compound in the material decreases, and the solid solubility increases. Therefore, by heating the material to a temperature as high as possible, the volume ratio of the compound containing Mg and Si is decreased and the solid solution amount is increased, which is effective in improving the heat-curability.

【0012】しかしながら高温加熱のみではこれら化合
物は完全には無くならないばかりか、化合物全体として
の体積率は減少するものの、高温加熱後の残存する個々
の化合物サイズは加熱前の化合物サイズよりも大きくな
る事が見出された。さらに熱間圧延時には加熱された材
料は圧延中に温度低下が生じ、圧延中及び圧延終了時に
前述のMg,Si化合物が再析出してしまう問題点が有
ることが明らかとなった。この再析出は前述の残存化合
物の粗大化と、熱間圧延中もしくは圧延終了直後に生じ
る再結晶粒界への優先的な析出・成長を生じる事が特徴
である。しかもこの析出反応は、比較的高い温度での反
応であるために析出速度が大きい事に加えて、熱間圧延
時の歪みもこの析出を促進するために、短時間で粗大な
析出相に成長してしまい、このような粗大な析出相は溶
体化処理時には固溶しにくい事が確認された。
However, not only these compounds are not completely eliminated by heating at a high temperature, but the volume ratio of the entire compound is reduced, but the size of each individual compound remaining after heating at a high temperature becomes larger than the size of the compound before heating. Things have been found. Further, it has been clarified that the temperature of the material heated during the hot rolling lowers during the rolling and that the above-mentioned Mg and Si compounds reprecipitate during the rolling and at the end of the rolling. This reprecipitation is characterized by coarsening of the above-mentioned residual compound and preferential precipitation / growth at the recrystallized grain boundary that occurs during hot rolling or immediately after the end of rolling. Moreover, since this precipitation reaction is a reaction at a relatively high temperature, the precipitation rate is high, and strain during hot rolling also promotes this precipitation, so that a coarse precipitation phase grows in a short time. It was confirmed that such a coarse precipitation phase is unlikely to form a solid solution during solution treatment.

【0013】それゆえこのような熱間圧延時の再析出を
抑制するためには、均質化処理等で高温に加熱した材料
を速やかに冷却して低温で圧延する事で、析出速度を下
げると共に再結晶粒を微細化して粒界への優先析出・成
長を分散することが有効で有ることを見出した。
Therefore, in order to suppress such reprecipitation during hot rolling, the material heated to a high temperature in a homogenizing treatment or the like is rapidly cooled and rolled at a low temperature to reduce the precipitation rate. It was found that it is effective to refine the recrystallized grains to disperse preferential precipitation / growth at grain boundaries.

【0014】本発明はかかる技術思想に基づいてなされ
たものであり、本発明において製造条件を規定した理由
を以下に述べる。
The present invention has been made based on such a technical idea, and the reason why the manufacturing conditions are defined in the present invention will be described below.

【0015】熱間圧延前の均質化処理での加熱温度は、
又は熱間圧延の途中で加熱する加熱温度はできる限り高
温にして可能な限りMg,Siの固溶度を上げる必要が
ある。しかして 480℃未満の加熱では固溶が十分ではな
く、 500℃以上が望ましい加熱温度である。また加熱温
度の上限は特に定めるものではなく、高温である方が望
ましく材料の固相線温度以下であれば良い。
The heating temperature in the homogenization treatment before hot rolling is
Alternatively, the heating temperature for heating in the course of hot rolling needs to be as high as possible to increase the solid solubility of Mg and Si as much as possible. However, heating below 480 ° C does not provide sufficient solid solution, and 500 ° C or higher is a desirable heating temperature. The upper limit of the heating temperature is not particularly limited, and it is preferable that the heating temperature is high, and the heating temperature may be lower than the solidus temperature of the material.

【0016】熱間圧延時に 360〜450 ℃の温度範囲で圧
延を実施する事が最も析出が進行しやすく、かつ再結晶
粒が粗大になりやすい条件である。従ってこの温度範囲
を短時間で冷却することが必要である。しかしてこの温
度範囲に15分以上晒されると前述の粗大な析出物を生じ
て加熱硬化性が減少してしまうものであり、10分以内で
あることが好ましい。
When hot rolling is carried out in the temperature range of 360 to 450 ° C., precipitation is most likely to proceed and recrystallized grains are likely to become coarse. Therefore, it is necessary to cool this temperature range in a short time. However, if exposed to this temperature range for 15 minutes or more, the above-mentioned coarse precipitates are generated and the heat-curability is reduced, and it is preferably within 10 minutes.

【0017】しかしながら鋳塊のような肉厚の厚いもの
では急速な冷却は困難であり、望ましい方法としては
肉厚の小さい鋳塊もしくは圧延板を使用して圧延中の冷
却が速やかに進むようにする、圧延時の圧下量を大き
くすることで急速に板厚を減少させ、短時間の内に冷却
されやすい肉厚まで圧延する、圧延途中で積極的に
水、油等の冷媒を圧延板にかけることで急速冷却を行う
等の方法が考えられる。本発明ではこれら条件の詳細ま
で規定するものではなく、前記温度・時間条件が満足さ
れれば良い。
However, it is difficult to rapidly cool a thick ingot such as an ingot, and a preferable method is to use an ingot or a rolled plate having a small wall thickness so that the cooling during the rolling progresses quickly. The plate thickness is rapidly reduced by increasing the rolling amount during rolling, and rolling is performed to a wall thickness that facilitates cooling in a short period of time. It is conceivable to use a method such as rapid cooling by applying. The present invention does not specify the details of these conditions, and it is sufficient that the temperature / time conditions are satisfied.

【0018】次に熱間圧延上がり温度は 360℃以下とす
る。これは熱間圧延上がり温度が360 ℃を越えると再結
晶粒が粗大化して、加熱硬化性が減少してしまうからで
ある。
Next, the hot rolling finish temperature is set to 360 ° C. or lower. This is because if the temperature after hot rolling exceeds 360 ° C, the recrystallized grains become coarse and the heat-hardening property decreases.

【0019】また熱間圧延が終了した板は冷間圧延を施
し、必要に応じて冷間圧延途中に中間焼鈍を施す、ある
いは施さずに所定の板厚とした後、 500℃以上の温度に
10秒以上加熱して溶体化処理を行う。しかして 500℃未
満の温度あるいは10秒未満の加熱では溶体化が十分に行
われないからである。なお加熱温度の上限は特に定める
ものではないが、固相線温度以下の温度で実施されるの
が通常である。また加熱時間も長時間であるほうが溶体
化か進み易く好ましいが、あまり長時間の加熱は経済的
に不利となることから、操業上の都合により加熱時間を
定めれば良い。
Further, the plate which has been hot rolled is subjected to cold rolling, and if necessary, subjected to intermediate annealing during the cold rolling, or to a predetermined plate thickness without being subjected to it, and then to a temperature of 500 ° C. or higher.
Heat for 10 seconds or more to perform solution treatment. However, if the temperature is less than 500 ° C or heating for less than 10 seconds, solution treatment is not sufficiently performed. The upper limit of the heating temperature is not particularly limited, but it is usually performed at a temperature below the solidus temperature. Further, it is preferable that the heating time is long so that the solution formation proceeds easily. However, since heating for a too long time is economically disadvantageous, the heating time may be set for convenience of operation.

【0020】[0020]

【実施例】表1に示す組成の合金を通常のDC鋳造にて
厚さ 400mm、幅1200mmの鋳塊とした。この合金を片面5
mmづつの面削後、これら合金に表2に示す熱処理及び熱
間圧延のいずれかの条件を表3に示すように施した。そ
して熱間圧延上がりの板厚は5mmとし、その後冷間圧延
にて1mmの板材とした。
Example An alloy having the composition shown in Table 1 was formed into a ingot having a thickness of 400 mm and a width of 1200 mm by ordinary DC casting. This alloy on one side 5
After chamfering by mm, these alloys were subjected to either heat treatment or hot rolling shown in Table 2 as shown in Table 3. The plate thickness after hot rolling was set to 5 mm and then cold rolled to a plate material of 1 mm.

【0021】なお表2の本発明工程である工程Aは熱間
圧延途中の板厚約 150mm、材料温度約 490℃において、
水溶性の油を含む冷媒にて強制冷却を行い、約6分間で
350℃に冷却をした後圧延を再開したものである。また
比較工程である工程B〜Dは熱間圧延の圧下量と圧延時
間を調整することにより表2の熱間圧延条件を達成し
た。
Step A, which is the process of the present invention shown in Table 2, is that the plate thickness during hot rolling is about 150 mm and the material temperature is about 490 ° C.
Perform forced cooling with a refrigerant containing water-soluble oil, and in about 6 minutes
After cooling to 350 ° C, rolling was restarted. In the comparative steps B to D, the hot rolling conditions shown in Table 2 were achieved by adjusting the reduction amount and rolling time of hot rolling.

【0022】このようにして得られた板材を引張試験に
より強度と伸び値を測定し、さらに成形後の塗装加熱の
シミュレートとして引張試験片を2%引張変形後に 170
℃×20分の加熱を行い、その後引張試験を行って強度を
測定した。結果を表3に併記した。
The strength and elongation of the plate material thus obtained were measured by a tensile test, and the tensile test piece was subjected to 2% tensile deformation to simulate coating heating after molding.
Heating was conducted at 20 ° C. for 20 minutes, and then a tensile test was performed to measure the strength. The results are also shown in Table 3.

【0023】[0023]

【表1】 [Table 1]

【0024】[0024]

【表2】 [Table 2]

【0025】[0025]

【表3】 [Table 3]

【0026】表3から明らかなように、本発明製造法に
よるものは加熱後の機械的性質に優れ、かつ加熱による
耐力増も大きいことが判る。これに対して本発明の範囲
を外れる比較製造法によるものは塗装加熱後の強度が低
く、加熱による硬化性が低いことが判る。
As is clear from Table 3, it can be seen that the manufacturing method of the present invention has excellent mechanical properties after heating and also has a large increase in yield strength due to heating. On the other hand, it can be seen that the comparative manufacturing method which is out of the scope of the present invention has low strength after coating heating and low curability by heating.

【0027】[0027]

【発明の効果】本発明によれば自動車、電気部品等に使
用されるAl−Mg−Si系合金の加熱硬化性を著しく
高める事が可能であり、部材の薄肉化、軽量化に顕著な
効果を奏するものである。従って本発明になる板材は二
輪車、乗用車等のホイールや外板のような自動車用部
品、成形加工後に焼付け塗装が行われる電気製品用の部
品あるいは機械部品等に好適である。
According to the present invention, it is possible to remarkably enhance the heat-hardening property of an Al-Mg-Si type alloy used for automobiles, electric parts, etc., and it is possible to remarkably reduce the thickness and weight of members. Is played. Therefore, the plate material according to the present invention is suitable for automobile parts such as wheels and outer plates of two-wheeled vehicles, passenger cars, etc., parts for electric appliances or baking parts for which baking is applied after forming.

───────────────────────────────────────────────────── フロントページの続き (72)発明者 佐々木 勝敏 東京都千代田区丸の内2丁目6番1号 古 河アルミニウム工業株式会社内 (72)発明者 渡辺 元 東京都千代田区丸の内2丁目6番1号 古 河アルミニウム工業株式会社内 ─────────────────────────────────────────────────── ─── Continuation of the front page (72) Inventor Katsutoshi Sasaki 2-6-1, Marunouchi, Chiyoda-ku, Tokyo Furukawa Aluminum Co., Ltd. (72) Inventor Gen 2 Watanabe 2-6-1, Marunouchi, Chiyoda-ku, Tokyo Furukawa Aluminum Co., Ltd.

Claims (1)

【特許請求の範囲】[Claims] 【請求項1】 Mg: 0.2〜2wt%、Si: 0.2〜2wt
%を含み、かつFe:2wt%以下、Cu:2wt%以下、
Zn:3wt%以下、Mn:2wt%以下、Cr: 0.5wt%
以下、Zr: 0.3wt%以下、Ti: 0.2wt%以下、B:
0.1wt%以下、Be:0.05wt%の1種もしくは2種以上
を含有し、残部が実質的にAlからなるAl合金鋳塊を
480℃以上に加熱して均質化処理した後、又は均質化処
理後熱間圧延途中で 480℃以上に加熱した後、熱間圧延
において 360〜450 ℃の温度範囲を15分未満で通過させ
て熱間圧延終了温度を 360℃以下とし、その後冷間圧延
を行い、さらに必要に応じて冷間圧延途中で中間焼鈍を
施して所定板厚とした後、 500℃以上の温度に10秒以上
加熱する溶体化処理を施すことを特徴とする加熱硬化性
に優れたAl−Mg−Si系合金板材の製造方法。
1. Mg: 0.2-2 wt%, Si: 0.2-2 wt%
%, And Fe: 2 wt% or less, Cu: 2 wt% or less,
Zn: 3 wt% or less, Mn: 2 wt% or less, Cr: 0.5 wt%
Below, Zr: 0.3 wt% or less, Ti: 0.2 wt% or less, B:
An Al alloy ingot containing 0.1 wt% or less and Be: 0.05 wt% of 1 type or 2 types or more, and the balance substantially consisting of Al.
After heating to 480 ° C or higher for homogenization, or after heating to 480 ° C or higher during hot rolling after homogenization, pass the temperature range of 360 to 450 ° C in less than 15 minutes in hot rolling. The hot rolling finish temperature is set to 360 ° C or less, then cold rolling is performed, and if necessary, intermediate annealing is performed in the middle of cold rolling to obtain a predetermined plate thickness, and then heating to a temperature of 500 ° C or more for 10 seconds or more. A method of manufacturing an Al-Mg-Si alloy sheet having excellent heat-hardening properties, which is characterized by performing a solution treatment.
JP8547993A 1993-03-19 1993-03-19 Method for producing Al-Mg-Si alloy sheet excellent in heat-curability Expired - Fee Related JP2925884B2 (en)

Priority Applications (1)

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Application Number Priority Date Filing Date Title
JP8547993A JP2925884B2 (en) 1993-03-19 1993-03-19 Method for producing Al-Mg-Si alloy sheet excellent in heat-curability

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JP2925884B2 JP2925884B2 (en) 1999-07-28

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Cited By (5)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
EP0730040A1 (en) * 1995-02-27 1996-09-04 The Furukawa Electric Co., Ltd. High-pressure cast aluminum alloy with excellent strength and toughness, method of producing the same and wheel disc used the same
EP0826072A1 (en) * 1995-05-11 1998-03-04 KAISER ALUMINUM &amp; CHEMICAL CORPORATION Improved damage tolerant aluminum 6xxx alloy
EP1484420A1 (en) * 2003-06-05 2004-12-08 Pechiney Rhenalu Use of a rolled or extruded aluminium alloy product having a high corrosion resistance
EP2177638A1 (en) * 2008-10-15 2010-04-21 "Impexmetal" S.A. Aluminium alloy, in particular for heat exchangers manufacturing
WO2016192040A1 (en) * 2015-06-02 2016-12-08 GM Global Technology Operations LLC Aluminum alloy for forming an axisymmetric article

Cited By (9)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
EP0730040A1 (en) * 1995-02-27 1996-09-04 The Furukawa Electric Co., Ltd. High-pressure cast aluminum alloy with excellent strength and toughness, method of producing the same and wheel disc used the same
EP0826072A1 (en) * 1995-05-11 1998-03-04 KAISER ALUMINUM &amp; CHEMICAL CORPORATION Improved damage tolerant aluminum 6xxx alloy
EP0826072A4 (en) * 1995-05-11 1998-07-15 Kaiser Aluminium Chem Corp Improved damage tolerant aluminum 6xxx alloy
EP1484420A1 (en) * 2003-06-05 2004-12-08 Pechiney Rhenalu Use of a rolled or extruded aluminium alloy product having a high corrosion resistance
EP1484421A1 (en) * 2003-06-05 2004-12-08 Pechiney Rhenalu Use of a rolled or extruded aluminium alloy product having a good corrosion resistance
FR2855833A1 (en) * 2003-06-05 2004-12-10 Pechiney Rhenalu LAMINATED OR ALUMINUM ALLOY WIRE WITH GOOD CORROSION RESISTANCE
EP2177638A1 (en) * 2008-10-15 2010-04-21 "Impexmetal" S.A. Aluminium alloy, in particular for heat exchangers manufacturing
WO2016192040A1 (en) * 2015-06-02 2016-12-08 GM Global Technology Operations LLC Aluminum alloy for forming an axisymmetric article
US10882104B2 (en) 2015-06-02 2021-01-05 GM Global Technology Operations LLC Aluminum alloy for forming an axisymmetric article

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