JP3821074B2 - Magnesium alloy plate and manufacturing method thereof - Google Patents

Magnesium alloy plate and manufacturing method thereof Download PDF

Info

Publication number
JP3821074B2
JP3821074B2 JP2002273494A JP2002273494A JP3821074B2 JP 3821074 B2 JP3821074 B2 JP 3821074B2 JP 2002273494 A JP2002273494 A JP 2002273494A JP 2002273494 A JP2002273494 A JP 2002273494A JP 3821074 B2 JP3821074 B2 JP 3821074B2
Authority
JP
Japan
Prior art keywords
magnesium alloy
rolling
grain size
crystal grain
magnesium
Prior art date
Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
Expired - Fee Related
Application number
JP2002273494A
Other languages
Japanese (ja)
Other versions
JP2004107743A (en
Inventor
善久 米満
将行 渋谷
幸一 山崎
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.)
Panasonic Corp
Nippon Steel Corp
Panasonic Holdings Corp
Original Assignee
Panasonic Corp
Sumitomo Metal Industries Ltd
Matsushita Electric Industrial Co Ltd
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 Panasonic Corp, Sumitomo Metal Industries Ltd, Matsushita Electric Industrial Co Ltd filed Critical Panasonic Corp
Priority to JP2002273494A priority Critical patent/JP3821074B2/en
Publication of JP2004107743A publication Critical patent/JP2004107743A/en
Application granted granted Critical
Publication of JP3821074B2 publication Critical patent/JP3821074B2/en
Anticipated expiration legal-status Critical
Expired - Fee Related legal-status Critical Current

Links

Images

Landscapes

  • Metal Rolling (AREA)

Description

【0001】
【発明の属する技術分野】
本発明は、プレス加工用マグネシウム合金板とその製造方法に関する。詳述すれば、本発明は、温間成形性、および有色塗装隠蔽性に優れたプレス加工用マグネシウム合金板とその製造方法に関するものである。
【0002】
【従来の技術】
実用マグネシウム合金は、Liを多量に含む特殊なものを除いて、比重は1.76〜1.83の間にあり、実用金属中最も小さく、比強度、比剛性が高いため、軽量化の手段として最適な金属材料である。
【0003】
特に、自動車の低燃費化、電気、電子機器の携帯性の観点から小型化、低消費電力化を進めるための剛性設計部品として有利である。
しかしながら、これまでダイキヤスト製品が僅かに用いられるのみであった。その原因の一つとして、マグネシウム合金以外の実用金属材料に較べて、マグネシウム合金は塑性加工性が著しく劣ることが挙げられる。
【0004】
ほとんどのマグネシウム合金の結晶構造は稠密六方格子であり、アルミニウム合金や銅合金の立方格子とは異なる。稠密六方格子では底面、柱面、錐面の3つのすべり面があるが、常温では底面すべりしか起こらないため、塑性加工性が悪くなる。しかし、再結晶温度以上になるとすべり面が増加し、塑性加工が可能となる。このような理由から、展伸材は再結晶温度以上でプレス加工される。一般的には温間成形法と呼称され、マグネシウム合金材の成形法はこの方法に限られている。
【0005】
ただ、このような温間成形法においても深絞り加工、曲げ加工等を施した場合、材料に割れの発生する頻度が高く問題となっていた。
そこで、延性の優れたマグネシウム合金板を得るため、特開2001−294966号公報には平均結晶粒径を0.1 〜30μm にすることが開示されている。また、延性、強度、深絞り性の優れたマグネシウム合金板を得るため、特開2001−200349号公報には結晶粒度を10μm 以下にすることが開示されている。
【0006】
しかし、上述のような範囲に平均結晶粒径を調整しても発生する割れは減少するが、実用上満足のいくレベルではなかった。
このようなことから、温間成形法に適したマグネシウム合金およびその製造法の確立が強く望まれた。
【0007】
また、マグネシウム合金を商品化する際は、圧延ないし鋳造により生じた表面傷を表面研磨にて取り除いてから、表面処理を実施するため、前処理の必要のないマグネシウム合金板の供給が強く望まれていた。
【0008】
【発明が解決しようとする課題】
本発明の目的は、工業的に大量に扱いやすく安価で成形性に優れたプレス加工用マグネシウム合金板とその製造方法を提供することである。
【0009】
【課題を解決するための手段】
上記の目的を達成するため、本発明者等は鋭意研究を行った結果、次に示すような知見を得ることができた。
【0010】
1)平均結晶粒径が同等でも温間成形性にバラツキが発生しやすい。
2)その傾向は結晶粒径の中に一部、粗粒が含まれている時、発生しやすい。
3)したがって、結晶粒径が整粒化されている材料は温間成形性に優れる。
【0011】
4)また、耐食性に著しく劣るマグネシウム合金板の表面処理は必須であり、コストの面から有色塗装が一般的である。
5)ところで、表面に最大粗さRmaxにて10μm を超える庇が発生しているマグネシウム合金板は有色塗装をしても庇は隠蔽できない。
【0012】
6)したがって、マグネシウム合金板の表面庇を隠蔽するには、表面最大粗さRmaxは10μm 以下でなければならない。
本発明は上記知見に基づいて完成されたものであり、その要旨は次の通りである。
【0013】
(1)質量%で、アルミニウム:2.5〜3.5%、亜鉛:0.6〜1.4%、マンガン:0.2〜1.0%、および残部マグネシウムおよび不純物である合金組成を有し、平均結晶粒径が10μm以下であり、そして結晶粒径の80%以上が、平均結晶粒径±(平均結晶粒径×0.5)μmの範囲にあることを特徴とするプレス加工用マグネシウム合金板。
【0014】
(2)表面最大粗さRmaxが10μm以下であることを特徴とする上記(1)に記載のプレス加工用マグネシウム合金板。
(3)質量%で、アルミニウム:2.5〜3.5%、亜鉛:0.6〜1.4%、マンガン:0.2〜1.0%、および残部マグネシウムおよび不純物である合金組成を有するマグネシウム合金材を、250〜350℃に加熱して圧延を行う第1圧延工程を1回または2回以上行うこと、および該第1圧延工程で得られた圧延板を250〜350℃に加熱する熱処理を行った後、複数パスの合計圧下率が12%以上の冷間圧延を行う第2圧延工程を2回以上行うことを特徴とするプレス加工用マグネシウム合金板の製造方法。
【0015】
【発明の実施の形態】
次に、本発明の実施の形態について説明する。
図1は、本発明にかかるプレス加工用マグネシウム合金板の製造装置の概略図である。
【0016】
図1において、アンコイラー1から連続的に巻き戻されたマグネシウム合金薄板コイルAは、加熱装置3により所定温度に加熱をされた後、圧延機4で圧延され、熱処理装置5により所定温度に加熱することで熱処理を施されてから、コイラー2で巻き取られる。必要により複数回この圧延を繰り返すことで所定厚さの圧延板とする。このときは所定厚さになるまで熱処理装置5は作動させない。
【0017】
加熱装置3による加熱温度は、好ましくは250 〜300 ℃であり、250 ℃未満のときには十分に圧延が行なわれず、結晶粒径のバラツキを抑えることが十分にできず、一方、300 ℃を超えると変形抵抗が低下し、幅縮みもしくは破断する場合がある。
【0018】
また、熱処理装置5による加熱温度も、好ましくは250 〜300 ℃であり、250 ℃未満のときには十分な再結晶化が実現できず、一方、300 ℃を超えると結晶粒が全体的に粗大化して最終的に平均結晶粒径を10μm 以下とすることができない場合がある。
【0019】
加熱装置3および熱処理装置5には、好ましくは、インダクションヒータが用いられる。圧延温度(圧延直前温度)は、圧延機入側、たとえば圧延機入側中心より400mm 手前の位置に設けた放射温度計6により測定する。熱処理温度(熱処理直後温度)は、熱処理装置出側、たとえば熱処理装置出側中心より400mm 後ろの位置に設けた放射温度計7により測定する。
【0020】
コイラー2で巻き取られた圧延材は、冷却後、今度は、巻き戻されて再び圧延機4で圧延され、合計圧下率が12%以上になるまで複数回の圧延を行う。好ましくは、パス当たり4〜6%の圧下率で3〜4パス行う。合計圧下量は割れ発生および圧縮帯発生の観点からは20%以下が好ましい。もちろん、この場合には、加熱装置3および熱処理装置5は停止する。
【0021】
冷間圧延に際して、合計圧下率が12%未満のときには、十分な細粒化が実現できず、20%を超えると割れと圧縮帯が発生することがある。また、1回の冷間圧延では、結晶粒径の均一化は十分でない。
【0022】
すなわち、従来は微細粒とすることを特に意図しており、合計圧下量を可及的に大きくすることが求められていたが、本発明にあっては冷間圧延に先立って熱処理を行い比較的圧下量の少ない冷間圧延を複数回行うことで結晶粒のバラツキを可及的少とすることを意図している。
【0023】
本発明においては、かかる温間圧延および冷間圧延の各圧延工程を、以下、便宜上、それぞれ第1圧延工程および第2圧延工程と云う。
別の態様として、図1の装置では第1圧延工程だけを行い、別途設けた圧延装置によって第2圧延工程を行うようにしてもよい。
【0024】
第1圧延工程および第2圧延工程の繰り返し数は、2セット (回) 以上であれば、特に制限はないが、好ましくは、2〜3セット (回) である。複数回の温間圧延および冷間圧延をセットで行うことで、平均結晶粒径の微細化と同時にそのバラツキの低減を実現するのである。
【0025】
かくして、本発明によれば、平均結晶粒径が10μm 以下であり、そして結晶粒径の80%以上が、平均結晶粒径±(平均結晶粒径×0.5)μm の範囲にあるマグネシウム合金板が得られる。
【0026】
このようにして得られるマグネシウム合金板には圧延による表面疵、つまり表面粗さが観察されるが、本発明の好適態様ではその表面粗さはRmax(最大表面粗さ) で10μm以下に制限する。有色塗装隠蔽性を確保するためである。そのような表面粗さは圧延ロールの表面粗さおよび圧延条件を変更することで調整できる。
【0027】
本発明にかかるプレス加工用マグネシウム合金板の合金組成は、いわゆる実用マグネシウム合金であって、特に制限されないが、好適態様にあっては、質量%で、アルミニウム:2.5〜3.5%、亜鉛:0.6〜1.4%、マンガン:0.2〜1.0%、および残部実質的にマグネシウムに限定されるが、かかる合金組成は、すでに規格、例えばASTMのAZ31Bに規定されており、本発明においてもそのような既知のマグネシウム合金をも包含するものである。
【0028】
ここに、本発明における合金組成の限定理由は、次の通りである。なお、本明細書において合金組成を表す「%」表示は、「質量%」を意味する。
Al:Alは、耐食性と機械的性質の改善のために配合され、2.5 %未満ではその所期の効果を十分に発揮できず、3.5 %を超えると、母材の加工性が低下する。
【0029】
Zn:Znは、耐食性と機械的性質の改善のために配合され、0.6 %未満ではその所期の効果を十分に発揮できず、1.4 %を超えると、母材の加工性が低下する。好ましくは、0.8 〜1.1 %である。
【0030】
Mn:Mnは、耐食性と強度の改善のために配合され、0.2 %未満ではその所期の効果を十分に発揮できず、1.0 %を超えると、MnAl金属間化合物を起点とする割れにより加工性が低下する。好ましくは、0.3 〜0.8 %である。
【0031】
その他、不可避不純物として、Fe、Si、Cu、Ni等が含まれることがあるが、それらは合計量として、0.050 %以下に制限することが好ましい。
次に、実施例によって本発明の作用効果についてさらに具体的に説明する。
【0032】
(実施例1)
本例で用いたマグネシウム合金板は、材質がASTMで規格されているAZ31B の焼鈍材 (Al:3.02%、Zn:0.88%、Mn:0.50%、Mg:残部) で寸法は厚さが2mm、幅が150mm であった。
【0033】
このマグネシウム合金板に、図1に示す装置を使って圧延を行った。まず、このマグネシウム合金板をアンコイラー1から連続的に巻き戻し、それぞれを加熱装置3により 250から350 ℃の温度範囲にて加熱して圧延を行い、250 ℃から350 ℃の温度範囲にて熱処理を行った。かかる温間圧延を板厚が0.78〜0.55mmになるまで繰り返した。
【0034】
その後、冷間圧延を熱処理なしで複数回繰り返し、250 ℃から350 ℃の温度範囲に加熱して熱処理を行った。その時の合計圧下率は5から20%であった。熱処理なしで複数回繰り返す冷間圧延を2セット( 回) 実施し、板厚を0.5mm とした。
【0035】
表1にこのときに得られたマグネシウム合金板の平均結晶粒径および粒径分布をまとめて示す。なお、圧延速度はいずれも4M/min に設定した。
ここでいう「粒径分布」とは、結晶粒径が(平均結晶粒径±(平均結晶粒径×0.5))の範囲にある比率であり、板厚中央部と板厚表層部の圧延方向と平行方向のミクロ観察を実施し、ミクロ写真からそれぞれN数50にて粒径を測定したものである。
【0036】
図2は、表1のNo.3 (本発明例) の試料のミクロ組織写真であり、平均粒径8μm 、粒径分布88%のミクロ組織を示す。
図3は、表1のNo.7 (比較例) の試料のミクロ組織写真であり、平均粒径9μm 、粒径分布74%のミクロ組織を示す。
【0037】
このようにして得られたマグネシウム合金板につき、温間成形性について評価した。
温間成形性の評価:
温間成形性は温間プレス加工により評価した。評価方法として、プレス速度30mm/s未満では商用生産を考えた場合、プレス速度が遅いため、生産数が少なくなるので×とした。プレス速度30mm/s以上では商用生産に耐え得る生産数となるため、○とした。
【0038】
圧延、焼鈍後のマグネシウム合金板から40mm角板を採取し、プレス速度を変化させプレスした。試験条件は、金型設定温度:250 ℃、ポンチ設定温度:250 ℃、プレス力:2〜3Ton 、シワ押さえ力:ゼロ、ポンチ肩:R=2mm、プレス深さ:15mm、潤滑:二硫化モリブデンとした。プレス加工し、割れの発生しなかった速度を限界プレス速度とし、その結果を併せて表1に示す。
【0039】
【表1】

Figure 0003821074
【0040】
このようにして得られた結果から、平均結晶粒径が10μm 以下であり、結晶粒径の80%以上が(平均結晶粒径±(平均結晶粒径×0.5))μm の範囲にあるマグネシウム合金板は優れた温間成形性を有することが判明した。
【0041】
(実施例2)
実施例1において得られたマグネシウム合金板のうち、圧延中に表面庇が見受けられた試料を供試材とし、表面庇部の表面最大粗さを測定し、これに有色塗装を行って有色塗装隠蔽性を評価した。
【0042】
有色塗装隠蔽性の評価:
圧延、焼鈍後のマグネシウム合金板から90mm角の試験片を採取し、脱脂、下地処理後、有色塗装を実施した。有色塗装に関して、塗膜厚は下塗りと上塗りを合わせて40〜50μm とした。有色塗装隠蔽性の判定は有色塗装後、表面庇および表面模様が観察されないものを○、表面庇および表面模様が観察されるものを×とした。
【0043】
結果は表2にまとめて示す。
【0044】
【表2】
Figure 0003821074
【0045】
このようにして得られた結果から、表面疵が発生しても表面最大粗さが10μm 以下であれば、有色塗装後は良好な外観を呈することが判明した。
【0046】
【発明の効果】
本発明によれば、温間成形性、有色塗装隠蔽性に優れたプレス加工用マグネシウム合金板を得ることができる。
【図面の簡単な説明】
【図1】マグネシウム合金板の製造装置の概略図である。
【図2】表1のNo.3の試料のミクロ組織写真である。
【図3】表1のNo.7の試料のミクロ組織写真である。
【符号の説明】
1:マグネシウムコイルアンコイラー
2:マグネシウムコイル巻き取りコイラー
3:加熱装置
4:圧延機
5:熱処理装置
6:放射温度計 (圧延機入側)
7:放射温度計 (熱処理装置出側)[0001]
BACKGROUND OF THE INVENTION
The present invention relates to a magnesium alloy plate for press working and a method for producing the same. More specifically, the present invention relates to a magnesium alloy plate for press working excellent in warm formability and colored paint concealing property, and a method for producing the same.
[0002]
[Prior art]
Practical magnesium alloys, except for special ones that contain a large amount of Li, have a specific gravity in the range of 1.76 to 1.83, the smallest among practical metals, and have high specific strength and specific rigidity. Material.
[0003]
In particular, it is advantageous as a rigid design component for promoting miniaturization and low power consumption from the viewpoint of fuel efficiency reduction of automobiles and portability of electric and electronic devices.
Until now, however, only a few die cast products have been used. One of the causes is that the magnesium alloy is remarkably inferior in plastic workability as compared with practical metal materials other than the magnesium alloy.
[0004]
The crystal structure of most magnesium alloys is a dense hexagonal lattice, which is different from the cubic lattice of aluminum and copper alloys. In the dense hexagonal lattice, there are three sliding surfaces, that is, a bottom surface, a column surface, and a conical surface, but since only bottom surface sliding occurs at room temperature, the plastic workability deteriorates. However, when the temperature exceeds the recrystallization temperature, the slip surface increases and plastic working becomes possible. For this reason, the wrought material is pressed at the recrystallization temperature or higher. Generally, it is called a warm forming method, and the forming method of the magnesium alloy material is limited to this method.
[0005]
However, even in such a warm forming method, when deep drawing, bending, or the like is performed, the frequency of occurrence of cracks in the material is high and has become a problem.
Therefore, in order to obtain a magnesium alloy sheet having excellent ductility, Japanese Patent Application Laid-Open No. 2001-294966 discloses that the average crystal grain size is 0.1 to 30 μm. In order to obtain a magnesium alloy sheet excellent in ductility, strength, and deep drawability, JP-A-2001-200349 discloses that the crystal grain size is 10 μm or less.
[0006]
However, even if the average crystal grain size is adjusted within the above range, cracks that occur are reduced, but the level is not satisfactory in practice.
For these reasons, it has been strongly desired to establish a magnesium alloy suitable for the warm forming method and a method for producing the same.
[0007]
In addition, when commercializing a magnesium alloy, it is strongly desired to supply a magnesium alloy plate that does not require pre-treatment because surface treatment is performed after removing surface scratches caused by rolling or casting by surface polishing. It was.
[0008]
[Problems to be solved by the invention]
An object of the present invention is to provide a magnesium alloy plate for press working , which is industrially easy to handle in large quantities, inexpensive and excellent in formability, and a method for producing the same.
[0009]
[Means for Solving the Problems]
In order to achieve the above object, the present inventors have conducted extensive research and, as a result, have obtained the following knowledge.
[0010]
1) Warm formability is likely to vary even if the average crystal grain size is the same.
2) This tendency tends to occur when some of the crystal grain size contains coarse grains.
3) Therefore, a material having a controlled crystal grain size is excellent in warm formability.
[0011]
4) In addition, the surface treatment of the magnesium alloy plate which is remarkably inferior in corrosion resistance is essential, and colored coating is generally used from the viewpoint of cost.
5) By the way, a magnesium alloy sheet having a surface with a maximum roughness Rmax of wrinkles exceeding 10 μm cannot be covered even with colored coating.
[0012]
6) Therefore, in order to hide the surface defects of the magnesium alloy plate, the maximum surface roughness Rmax must be 10 μm or less.
The present invention has been completed based on the above findings, and the gist thereof is as follows.
[0013]
(1) The alloy composition which is aluminum: 2.5-3.5%, zinc: 0.6-1.4%, manganese: 0.2-1.0%, and the balance magnesium and impurities by mass%. a, the average crystal grain size is 10μm or less, and more than 80% of the grain size, the press is characterized in that the range of the average grain size ± (average grain size × 0.5) [mu] m processing use magnesium alloy plate.
[0014]
(2) The magnesium alloy plate for press working as described in (1) above, wherein the maximum surface roughness Rmax is 10 μm or less.
(3) The alloy composition which is aluminum: 2.5-3.5%, zinc: 0.6-1.4%, manganese: 0.2-1.0%, and the balance magnesium and impurities in mass%. 1st rolling process which heats and heats the magnesium alloy material which has it to 250-350 degreeC is performed once or 2 times or more, and the rolled sheet obtained at this 1st rolling process is heated to 250-350 degreeC A method for producing a magnesium alloy sheet for press working, comprising: performing a second rolling step of performing cold rolling with a total rolling reduction of a plurality of passes of 12% or more after performing the heat treatment.
[0015]
DETAILED DESCRIPTION OF THE INVENTION
Next, an embodiment of the present invention will be described.
FIG. 1 is a schematic view of an apparatus for producing a magnesium alloy sheet for press working according to the present invention.
[0016]
In FIG. 1, the magnesium alloy thin plate coil A continuously unwound from the uncoiler 1 is heated to a predetermined temperature by the heating device 3, then rolled by the rolling mill 4, and heated to the predetermined temperature by the heat treatment device 5. After being subjected to heat treatment, it is wound up by the coiler 2. If necessary, the rolling is repeated a plurality of times to obtain a rolled sheet having a predetermined thickness. At this time, the heat treatment apparatus 5 is not operated until the predetermined thickness is reached.
[0017]
The heating temperature by the heating device 3 is preferably 250 to 300 ° C. When the temperature is less than 250 ° C., the rolling is not sufficiently performed, and the variation in the crystal grain size cannot be sufficiently suppressed. Deformation resistance decreases, and width may shrink or break.
[0018]
Also, the heating temperature by the heat treatment apparatus 5 is preferably 250 to 300 ° C., and if it is less than 250 ° C., sufficient recrystallization cannot be realized, while if it exceeds 300 ° C., the crystal grains are coarsened as a whole. Finally, the average crystal grain size may not be 10 μm or less.
[0019]
For the heating device 3 and the heat treatment device 5, an induction heater is preferably used. The rolling temperature (temperature immediately before rolling) is measured by a radiation thermometer 6 provided at a position 400 mm before the rolling mill entrance side, for example, the center of the rolling mill entrance side. The heat treatment temperature (temperature immediately after the heat treatment) is measured by a radiation thermometer 7 provided at a position 400 mm behind the heat treatment apparatus exit side, for example, the center of the heat treatment apparatus exit side.
[0020]
The rolled material wound up by the coiler 2 is cooled and then unwound and then rolled again by the rolling mill 4 and rolled a plurality of times until the total rolling reduction becomes 12% or more. Preferably, 3-4 passes are performed at a rolling reduction of 4-6% per pass. The total amount of rolling reduction is preferably 20% or less from the viewpoint of occurrence of cracks and compression bands. Of course, in this case, the heating device 3 and the heat treatment device 5 are stopped.
[0021]
In cold rolling, if the total rolling reduction is less than 12%, sufficient fine graining cannot be realized, and if it exceeds 20%, cracks and compression bands may occur. In addition, in one cold rolling, the crystal grain size is not sufficiently uniform.
[0022]
That is, in the past, it was specifically intended to make fine particles, and the total reduction amount was required to be as large as possible, but in the present invention, heat treatment was performed prior to cold rolling for comparison. It is intended to minimize the variation of crystal grains by performing cold rolling with a small amount of rolling reduction a plurality of times.
[0023]
In the present invention, such warm rolling and cold rolling processes are hereinafter referred to as a first rolling process and a second rolling process, respectively, for convenience.
As another aspect, only the first rolling process may be performed in the apparatus of FIG. 1 and the second rolling process may be performed by a separately provided rolling apparatus.
[0024]
The number of repetitions of the first rolling step and the second rolling step is not particularly limited as long as it is 2 sets (times) or more, but preferably 2 to 3 sets (times). By performing a plurality of times of warm rolling and cold rolling as a set, the average crystal grain size is reduced and the variation is reduced simultaneously.
[0025]
Thus, according to the present invention, there is provided a magnesium alloy plate having an average crystal grain size of 10 μm or less and 80% or more of the crystal grain size in the range of average crystal grain size ± (average crystal grain size × 0.5) μm. can get.
[0026]
In the magnesium alloy sheet thus obtained, surface defects due to rolling, that is, surface roughness, are observed. In a preferred embodiment of the present invention, the surface roughness is limited to Rmax (maximum surface roughness) of 10 μm or less. . This is to ensure the color paint concealment. Such surface roughness can be adjusted by changing the surface roughness of the rolling roll and the rolling conditions.
[0027]
The alloy composition of the magnesium alloy plate for press working according to the present invention is a so-called practical magnesium alloy, and is not particularly limited. However, in a preferred embodiment, the mass ratio is aluminum: 2.5 to 3.5%. Zinc: 0.6-1.4%, Manganese: 0.2-1.0%, and the balance is substantially limited to magnesium, but such alloy composition is already specified in the standard, eg ASTM AZ31B In the present invention, such a known magnesium alloy is also included.
[0028]
Here, the reasons for limiting the alloy composition in the present invention are as follows. In the present specification, “%” indicating an alloy composition means “mass%”.
Al: Al is blended for improving corrosion resistance and mechanical properties. If it is less than 2.5%, the desired effect cannot be sufficiently exhibited, and if it exceeds 3.5%, the workability of the base material is lowered.
[0029]
Zn: Zn is blended for improving corrosion resistance and mechanical properties. If the content is less than 0.6%, the desired effect cannot be sufficiently exhibited. If the content exceeds 1.4%, the workability of the base material is lowered. Preferably, it is 0.8 to 1.1%.
[0030]
Mn: Mn is added to improve corrosion resistance and strength. If it is less than 0.2%, the desired effect cannot be fully achieved. If it exceeds 1.0%, workability is caused by cracks originating from MnAl intermetallic compounds. Decreases. Preferably, it is 0.3 to 0.8%.
[0031]
In addition, Fe, Si, Cu, Ni, and the like may be included as unavoidable impurities, but these are preferably limited to 0.050% or less as a total amount.
Next, the effects of the present invention will be described more specifically with reference to examples.
[0032]
(Example 1)
The magnesium alloy plate used in this example is AZ31B annealed material (Al: 3.02%, Zn: 0.88%, Mn: 0.50%, Mg: balance), and the dimensions are 2mm in thickness. The width was 150mm.
[0033]
The magnesium alloy sheet was rolled using the apparatus shown in FIG. First, the magnesium alloy sheet is continuously unwound from the uncoiler 1, each is heated and heated in the temperature range of 250 to 350 ° C. by the heating device 3, and the heat treatment is performed in the temperature range of 250 to 350 ° C. went. Such warm rolling was repeated until the plate thickness became 0.78 to 0.55 mm.
[0034]
Thereafter, cold rolling was repeated several times without heat treatment, and heat treatment was performed by heating to a temperature range of 250 ° C to 350 ° C. The total rolling reduction at that time was 5 to 20%. Two sets (times) of cold rolling repeated multiple times without heat treatment were performed, and the plate thickness was set to 0.5 mm.
[0035]
Table 1 summarizes the average crystal grain size and grain size distribution of the magnesium alloy sheet obtained at this time. The rolling speed was set to 4M / min.
“Grain size distribution” as used herein is a ratio in which the crystal grain size is in the range of (average crystal grain size ± (average crystal grain size × 0.5)), and the rolling direction of the plate thickness center portion and the plate thickness surface layer portion. The particle size was measured at an N number of 50 from each microphotograph.
[0036]
FIG. 2 is a microstructure photograph of the sample No. 3 (example of the present invention) in Table 1, showing a microstructure with an average particle size of 8 μm and a particle size distribution of 88%.
FIG. 3 is a microstructure photograph of the sample No. 7 (comparative example) in Table 1, showing a microstructure with an average particle size of 9 μm and a particle size distribution of 74%.
[0037]
The magnesium alloy sheet thus obtained was evaluated for warm formability.
Evaluation of warm formability:
Warm formability was evaluated by warm pressing. As the evaluation method, when commercial production was considered at a press speed of less than 30 mm / s, the press speed was slow, so the number of production was reduced, and therefore, x was assigned. Since the production number can withstand commercial production at a press speed of 30 mm / s or higher, it was marked as “Good”.
[0038]
A 40 mm square plate was taken from the magnesium alloy plate after rolling and annealing, and was pressed while changing the pressing speed. Test conditions are: mold set temperature: 250 ° C., punch set temperature: 250 ° C., press force: 2-3 Ton, wrinkle holding force: zero, punch shoulder: R = 2 mm, press depth: 15 mm, lubrication: molybdenum disulfide It was. The speed at which pressing was performed and cracks did not occur was defined as the critical pressing speed, and the results are also shown in Table 1.
[0039]
[Table 1]
Figure 0003821074
[0040]
From the results thus obtained, a magnesium alloy having an average crystal grain size of 10 μm or less and 80% or more of the crystal grain size in the range of (average crystal grain size ± (average crystal grain size × 0.5)) μm The plate was found to have excellent warm formability.
[0041]
(Example 2)
Of the magnesium alloy plate obtained in Example 1, a sample in which surface flaws were observed during rolling was used as a test material, and the maximum surface roughness of the surface flaws was measured. Concealment was evaluated.
[0042]
Evaluation of color paint concealment:
A 90 mm square test piece was taken from the magnesium alloy sheet after rolling and annealing, and after degreasing and base treatment, colored coating was performed. For colored coatings, the coating thickness was 40-50 μm for both the undercoat and topcoat. The determination of the color paint concealment property was evaluated as “◯” when the surface wrinkles and surface patterns were not observed after the color coating, and “X” when the surface wrinkles and surface patterns were observed.
[0043]
The results are summarized in Table 2.
[0044]
[Table 2]
Figure 0003821074
[0045]
From the results thus obtained, it was found that even if surface flaws occur, if the maximum surface roughness is 10 μm or less, a good appearance is obtained after colored coating.
[0046]
【The invention's effect】
ADVANTAGE OF THE INVENTION According to this invention, the magnesium alloy plate for press work excellent in warm formability and colored coating concealment property can be obtained.
[Brief description of the drawings]
FIG. 1 is a schematic view of an apparatus for producing a magnesium alloy plate.
FIG. 2 is a microstructure photograph of a sample No. 3 in Table 1.
FIG. 3 is a microstructure photograph of a sample No. 7 in Table 1.
[Explanation of symbols]
1: Magnesium coil uncoiler 2: Magnesium coil winding coiler 3: Heating device 4: Rolling mill 5: Heat treatment device 6: Radiation thermometer (on the rolling mill)
7: Radiation thermometer (outside of heat treatment equipment)

Claims (3)

質量%で、アルミニウム:2.5〜3.5%、亜鉛:0.6〜1.4%、マンガン:0.2〜1.0%、および残部マグネシウムおよび不純物である合金組成を有し、平均結晶粒径が10μm以下であり、そして結晶粒径の80%以上が、平均結晶粒径±(平均結晶粒径×0.5)μmの範囲にあることを特徴とするプレス加工用マグネシウム合金板。Having an alloy composition of, by weight, aluminum: 2.5-3.5%, zinc: 0.6-1.4%, manganese: 0.2-1.0%, and the balance magnesium and impurities , Magnesium alloy for press working, wherein the average crystal grain size is 10 μm or less, and 80% or more of the crystal grain size is in the range of average crystal grain size ± (average crystal grain size × 0.5) μm Board. 表面最大粗さRmaxが10μm以下であることを特徴とする請求項1に記載のプレス加工用マグネシウム合金板。The magnesium alloy plate for press working according to claim 1, wherein the maximum surface roughness Rmax is 10 µm or less. 質量%で、アルミニウム:2.5〜3.5%、亜鉛:0.6〜1.4%、マンガン:0.2〜1.0%、および残部マグネシウムおよび不純物である合金組成を有するマグネシウム合金材を、250〜350℃に加熱して圧延を行う第1圧延工程を1回または2回以上行うこと、および該第1圧延工程で得られた圧延板を250〜350℃に加熱する熱処理を行った後、複数パスの合計圧下率が12%以上の冷間圧延を行う第2圧延工程を2回以上行うことを特徴とするプレス加工用マグネシウム合金板の製造方法。Magnesium alloy having an alloy composition of aluminum: 2.5-3.5%, zinc: 0.6-1.4%, manganese: 0.2-1.0%, and the balance magnesium and impurities in mass% A first rolling step of heating the material to 250 to 350 ° C. to perform rolling is performed once or twice or more, and a heat treatment for heating the rolled plate obtained in the first rolling step to 250 to 350 ° C. A method for producing a magnesium alloy sheet for press working, wherein the second rolling step of performing cold rolling with a total rolling reduction of a plurality of passes of 12% or more is performed twice or more.
JP2002273494A 2002-09-19 2002-09-19 Magnesium alloy plate and manufacturing method thereof Expired - Fee Related JP3821074B2 (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP2002273494A JP3821074B2 (en) 2002-09-19 2002-09-19 Magnesium alloy plate and manufacturing method thereof

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP2002273494A JP3821074B2 (en) 2002-09-19 2002-09-19 Magnesium alloy plate and manufacturing method thereof

Publications (2)

Publication Number Publication Date
JP2004107743A JP2004107743A (en) 2004-04-08
JP3821074B2 true JP3821074B2 (en) 2006-09-13

Family

ID=32270234

Family Applications (1)

Application Number Title Priority Date Filing Date
JP2002273494A Expired - Fee Related JP3821074B2 (en) 2002-09-19 2002-09-19 Magnesium alloy plate and manufacturing method thereof

Country Status (1)

Country Link
JP (1) JP3821074B2 (en)

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
WO2009051176A1 (en) 2007-10-16 2009-04-23 Ihi Metaltech Co., Ltd. Magnesium alloy hot-rolling mill

Families Citing this family (13)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JP4127126B2 (en) * 2003-06-10 2008-07-30 住友金属工業株式会社 Magnesium alloy plate manufacturing method
JP2005333321A (en) * 2004-05-19 2005-12-02 Pioneer Electronic Corp Speaker device and method for manufacturing magnesium edge therefor
JP4476787B2 (en) * 2004-11-17 2010-06-09 三菱アルミニウム株式会社 Method for producing magnesium alloy sheet with excellent press formability
JP4780601B2 (en) * 2004-11-18 2011-09-28 三菱アルミニウム株式会社 Magnesium alloy plate excellent in press formability and manufacturing method thereof
JP4429877B2 (en) * 2004-11-18 2010-03-10 三菱アルミニウム株式会社 Method for producing magnesium alloy sheet having fine crystal grains
JP4253846B2 (en) * 2004-11-30 2009-04-15 住友電気工業株式会社 Magnesium alloy wire, method for producing the same, and magnesium alloy molded body
JP2006185490A (en) * 2004-12-27 2006-07-13 Magnes:Kk Information recording medium and its manufacturing method
JP2006239748A (en) * 2005-03-04 2006-09-14 Sumitomo Metal Ind Ltd Method for producing magnesium alloy
JP5083148B2 (en) * 2008-09-29 2012-11-28 住友電気工業株式会社 Magnesium alloy parts
JP5637386B2 (en) 2010-02-08 2014-12-10 住友電気工業株式会社 Magnesium alloy plate
JP5716886B2 (en) * 2010-07-20 2015-05-13 住友電気工業株式会社 Magnesium alloy coil material and manufacturing method thereof
KR101459732B1 (en) * 2012-12-28 2014-11-13 주식회사 포스코 Method for improving surface quality magnesium alloy plate
WO2016121722A1 (en) * 2015-01-27 2016-08-04 株式会社三徳 Magnesium-lithium alloy, rolled material and shaped article

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
WO2009051176A1 (en) 2007-10-16 2009-04-23 Ihi Metaltech Co., Ltd. Magnesium alloy hot-rolling mill

Also Published As

Publication number Publication date
JP2004107743A (en) 2004-04-08

Similar Documents

Publication Publication Date Title
JP3821074B2 (en) Magnesium alloy plate and manufacturing method thereof
JP5880811B2 (en) Magnesium alloy cast material, magnesium alloy cast coil material, magnesium alloy wrought material, magnesium alloy joint material, method for producing magnesium alloy cast material, method for producing magnesium alloy wrought material, and method for producing magnesium alloy member
JP3558628B2 (en) Magnesium alloy plate and method for producing the same
WO2008029497A1 (en) Magnesium alloy member and method for producing the same
US20110318603A1 (en) Magnesium alloy member
EP2447381A1 (en) Magnesium alloy plate
JP2017160542A (en) Magnesium alloy casting material, magnesium alloy cast coil material, wrought magnesium alloy material, magnesium alloy member, magnesium alloy joint material, and method for producing magnesium alloy casting material
JP3521863B2 (en) Manufacturing method of magnesium alloy sheet
CN108699641A (en) The manufacturing method of Al-Mg-Si system alloy material, Al-Mg-Si system alloy plate and Al-Mg-Si system alloy plate
EP2453031A1 (en) Magnesium alloy plate
US9181608B2 (en) Magnesium alloy sheet
WO2013187419A1 (en) Magnesium alloy plate and magnesium alloy member
JP2020033605A (en) Al-Mg-Si-BASED ALLOY SHEET
JP5757085B2 (en) Magnesium alloy coil material, magnesium alloy coil material manufacturing method, magnesium alloy member, and magnesium alloy member manufacturing method
JP5688674B2 (en) Magnesium alloy coil material, magnesium alloy plate, and method for producing magnesium alloy coil material
JP2020033607A (en) Al-Mg-Si-BASED ALLOY SHEET
JP6274483B2 (en) Magnesium alloy coil material and method for producing magnesium alloy coil material
CN108699663A (en) The manufacturing method of Al-Mg-Si system alloy plate
TW201738390A (en) Method for producing al-mg-Si alloy plate
JP6136037B2 (en) Magnesium alloy cast material, magnesium alloy cast coil material, magnesium alloy wrought material, magnesium alloy joint material, method for producing magnesium alloy cast material, method for producing magnesium alloy wrought material, and method for producing magnesium alloy member
JPWO2020004561A1 (en) Hot-rolled steel sheets, high-strength cold-rolled steel sheets and their manufacturing methods
WO2011071023A1 (en) Magnesium alloy member
JP2006283112A (en) Aluminum alloy sheet for drink can barrel, and method for producing the same
EP2559780A1 (en) Impact-resistant member
JP2020033606A (en) MANUFACTURING METHOD OF Al-Mg-Si-BASED ALLOY SHEET

Legal Events

Date Code Title Description
A621 Written request for application examination

Free format text: JAPANESE INTERMEDIATE CODE: A621

Effective date: 20041111

A977 Report on retrieval

Free format text: JAPANESE INTERMEDIATE CODE: A971007

Effective date: 20060203

A131 Notification of reasons for refusal

Free format text: JAPANESE INTERMEDIATE CODE: A131

Effective date: 20060221

A521 Written amendment

Free format text: JAPANESE INTERMEDIATE CODE: A523

Effective date: 20060414

TRDD Decision of grant or rejection written
A01 Written decision to grant a patent or to grant a registration (utility model)

Free format text: JAPANESE INTERMEDIATE CODE: A01

Effective date: 20060530

A61 First payment of annual fees (during grant procedure)

Free format text: JAPANESE INTERMEDIATE CODE: A61

Effective date: 20060612

R150 Certificate of patent or registration of utility model

Free format text: JAPANESE INTERMEDIATE CODE: R150

FPAY Renewal fee payment (event date is renewal date of database)

Free format text: PAYMENT UNTIL: 20100630

Year of fee payment: 4

FPAY Renewal fee payment (event date is renewal date of database)

Free format text: PAYMENT UNTIL: 20100630

Year of fee payment: 4

FPAY Renewal fee payment (event date is renewal date of database)

Free format text: PAYMENT UNTIL: 20110630

Year of fee payment: 5

FPAY Renewal fee payment (event date is renewal date of database)

Free format text: PAYMENT UNTIL: 20110630

Year of fee payment: 5

S533 Written request for registration of change of name

Free format text: JAPANESE INTERMEDIATE CODE: R313533

R350 Written notification of registration of transfer

Free format text: JAPANESE INTERMEDIATE CODE: R350

FPAY Renewal fee payment (event date is renewal date of database)

Free format text: PAYMENT UNTIL: 20110630

Year of fee payment: 5

S111 Request for change of ownership or part of ownership

Free format text: JAPANESE INTERMEDIATE CODE: R313117

FPAY Renewal fee payment (event date is renewal date of database)

Free format text: PAYMENT UNTIL: 20110630

Year of fee payment: 5

R350 Written notification of registration of transfer

Free format text: JAPANESE INTERMEDIATE CODE: R350

FPAY Renewal fee payment (event date is renewal date of database)

Free format text: PAYMENT UNTIL: 20110630

Year of fee payment: 5

FPAY Renewal fee payment (event date is renewal date of database)

Free format text: PAYMENT UNTIL: 20120630

Year of fee payment: 6

FPAY Renewal fee payment (event date is renewal date of database)

Free format text: PAYMENT UNTIL: 20130630

Year of fee payment: 7

FPAY Renewal fee payment (event date is renewal date of database)

Free format text: PAYMENT UNTIL: 20130630

Year of fee payment: 7

S111 Request for change of ownership or part of ownership

Free format text: JAPANESE INTERMEDIATE CODE: R313111

FPAY Renewal fee payment (event date is renewal date of database)

Free format text: PAYMENT UNTIL: 20130630

Year of fee payment: 7

R350 Written notification of registration of transfer

Free format text: JAPANESE INTERMEDIATE CODE: R350

LAPS Cancellation because of no payment of annual fees