JP2001152302A - Aluminum alloy sheet excellent in press formability, and its manufacturing method - Google Patents
Aluminum alloy sheet excellent in press formability, and its manufacturing methodInfo
- Publication number
- JP2001152302A JP2001152302A JP33745299A JP33745299A JP2001152302A JP 2001152302 A JP2001152302 A JP 2001152302A JP 33745299 A JP33745299 A JP 33745299A JP 33745299 A JP33745299 A JP 33745299A JP 2001152302 A JP2001152302 A JP 2001152302A
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- Prior art keywords
- temperature
- aluminum alloy
- press formability
- room temperature
- alloy sheet
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Abstract
Description
【0001】[0001]
【発明の属する技術分野】本発明は、成形性に優れる、
自動車ボディシート等に好適なアルミニウム合金板およ
びその製造方法に関する。TECHNICAL FIELD The present invention relates to a mold having excellent moldability,
The present invention relates to an aluminum alloy sheet suitable for an automobile body sheet and the like and a method for producing the same.
【0002】[0002]
【従来の技術】近年、自動車の燃費向上を目的とした車
体軽量化の要望が高まっており、軽量化手段の一つとし
て自動車ボディシート等へのアルミニウム合金板の使用
が行われている。自動車のボディシート用材料として
は、プレス成形性に優れるだけではなく、塗装焼付後の
強度や、耐食性等に優れることが要求される。現在使用
されている自動車ボディシ−ト用アルミニウム合金とし
ては、非熱処理型のAl−Mg系合金と、熱処理型のA
l−Mg−Si系とが用いられている。2. Description of the Related Art In recent years, there has been an increasing demand for weight reduction of a vehicle body for the purpose of improving fuel efficiency of an automobile. As one of means for reducing the weight, use of an aluminum alloy plate for an automobile body sheet or the like has been performed. A material for an automobile body sheet is required to have not only excellent press formability but also excellent strength after baking, corrosion resistance, and the like. Currently used aluminum alloys for automobile body sheets include a non-heat treated Al-Mg alloy and a heat treated A
An l-Mg-Si system is used.
【0003】Al−Mg系合金は、Mg含有量の増加と
ともに延性が向上することから、成形性に優れたアルミ
ニウム合金として、我が国では自動車ボデイパネルに多
用されている。しかしながら、Al−Mg系合金では、
Al−Mg−Si系合金より成形性は優れているもの
の、プレス成形の際にストレッチャー−ストレイン模様
が現れて表面品位を損なう場合があることや、塗装焼付
時に軟化してしまい、耐デント性に劣るという問題点が
ある。[0003] Al-Mg based alloys have been widely used in automobile body panels in Japan as aluminum alloys having excellent formability, since ductility is improved with an increase in Mg content. However, in Al-Mg based alloys,
Although it has better formability than Al-Mg-Si alloys, the stretcher-strain pattern may appear during press forming to impair the surface quality, or it may soften during baking and dent resistance. There is a problem that it is inferior.
【0004】一方、Al−Mg−Si系合金で本質的に
ストレッチャー−ストレイン模様はほとんど出現しない
ことや、塗装焼付工程の熱処理を活用して降伏強度の上
昇も図り得るという長所を有するが、Al−Mg系合金
に比べて成形性に劣るという問題点があり、自動車ボデ
ィパネル用としては、その適用に限界があった。このよ
うに自動車ボデイパネル用アルミニウム合金としては、
プレス成形性に優れるとともに、プレス後の表面品位に
も優れ、塗装焼付によって十分な強度がえられることが
求められている。On the other hand, the Al-Mg-Si-based alloy has advantages in that a stretcher-strain pattern essentially does not substantially appear, and that the yield strength can be increased by utilizing heat treatment in a coating baking process. There is a problem that the formability is inferior to that of an Al-Mg alloy, and there is a limit in its application to an automobile body panel. Thus, as an aluminum alloy for automobile body panels,
It is required to have excellent press formability, excellent surface quality after pressing, and sufficient strength by paint baking.
【0005】[0005]
【発明が解決しようとする課題】このような要求特性に
対して、例えば特開平1−287244号公報では、時
効硬化性を有するAl−Cu−Mg−Si系合金を芯材
として、良好な成形性を有し、かつストレッチャー−ス
トレイン模様も問題のない純Alを皮材としたアルミニ
ウム合金合わせ板が提案されており、プレス成形性と塗
装焼付硬化性が両立されている。しかしながら、合わせ
板では製造コストが高くなるとともに、端面において異
種金属接触腐食を起こす懸念がある。本発明は、単板で
5000系合金に匹敵するプレス成形性を有するととも
に、塗装焼付によって十分な強度が得られる自動車用ア
ルミニウム合金板を提供することを目的としたものであ
る。To cope with such required characteristics, for example, Japanese Unexamined Patent Publication No. 1-287244 discloses that an Al-Cu-Mg-Si alloy having age-hardening property is used as a core material to form a good molding. There has been proposed an aluminum alloy laminated plate using pure Al as a skin material, which has properties and has no problem with a stretcher-strain pattern, and achieves both press formability and paint bake hardenability. However, there is a concern that the manufacturing cost of the plywood increases and that contact corrosion of dissimilar metals occurs on the end face. SUMMARY OF THE INVENTION An object of the present invention is to provide an aluminum alloy sheet for automobiles having a single plate having press formability comparable to that of a 5000 series alloy and having sufficient strength obtained by coating and baking.
【0006】[0006]
【課題を解決するための手段】発明者らは、上記の目的
を達成するために、先ずアルミニウム合金板の成形性に
及ぼす材料因子について種々検討した。その結果、Al
−Mg−Si系をベースにCuを添加した合金におい
て、溶体化後室温近傍の温度で形成される溶質原子から
構成されるクラスター(以下低温クラスター)を形成さ
せると、(TS−YS)値が高くなり、その値が130
MPa以上あれば5000系合金と同等あるいはそれ以
上のプレス成形性が得られることを見出した。しかし、
この低温クラスターは、塗装焼付時のG.P.ゾーンの
析出を阻害し、塗装焼付け処理時には大きな強度上昇は
期待できないが、合金成分および製造方法を特定するこ
とによって、塗装焼付により軟化してしまうAl−Mg
系合金を上回る、十分な強度が得られることもわかっ
た。Means for Solving the Problems In order to achieve the above object, the inventors first studied various factors affecting the formability of an aluminum alloy sheet. As a result, Al
In an alloy containing Cu as a base based on an Mg-Si system, when a cluster (hereinafter referred to as a low-temperature cluster) formed of solute atoms formed at a temperature near room temperature after solution is formed, the (TS-YS) value becomes Higher and its value is 130
It has been found that a press formability equal to or higher than that of the 5000 series alloy can be obtained if the pressure is at least MPa. But,
This low-temperature cluster is used for G.I. P. Al-Mg, which hinders the precipitation of the zone and cannot be expected to have a large increase in strength at the time of paint baking, is softened by paint baking by specifying the alloy components and manufacturing method.
It was also found that sufficient strength could be obtained, exceeding that of the base alloy.
【0007】本発明は上記の知見に基づいて得られたも
ので、その要旨とするところは、 (1)mass%で、Mg:0.1〜0.6%、Si:
1.2超〜1.7%、Mg+Si:2%以下、Cu:
0.5〜1.5%を含有し、残部がAlおよび不可避的
不純物からなり、かつ、プレス前のTS(引張強さ)と
YS(0.2%耐力)において、(TS−YS)の値が
130MPa以上であることを特徴とするプレス成形性
に優れたアルミニウム合金板。 (2)mass%で、Ti:0.005〜0.15%、
B:0.0001〜0.05%、Mn:0.03〜0.
4%、Cr:0.02〜0.15%、Fe:0.03〜
0.3%、Zn:0.03〜1%のうち1種または2種
以上を、さらに含有することを特徴とする前記(1)に
記載のプレス成形性に優れたアルミニウム合金板。The present invention has been obtained based on the above findings, and its gist is as follows: (1) mass%, Mg: 0.1 to 0.6%, Si:
More than 1.2 to 1.7%, Mg + Si: 2% or less, Cu:
0.5-1.5%, the balance consists of Al and unavoidable impurities, and in TS (tensile strength) and YS (0.2% proof stress) before pressing, (TS-YS) An aluminum alloy plate excellent in press formability, having a value of 130 MPa or more. (2) mass%, Ti: 0.005 to 0.15%,
B: 0.0001 to 0.05%, Mn: 0.03 to 0.
4%, Cr: 0.02 to 0.15%, Fe: 0.03 to
The aluminum alloy sheet having excellent press formability according to the above (1), further comprising one or more of 0.3% and Zn: 0.03 to 1%.
【0008】(3)冷間圧延後、450〜580℃の温
度で溶体化処理を施した後に15℃/s以上の冷却速度
で室温以上70℃以下まで冷却することを特徴とする前
記(1)または(2)に記載のプレス成形性に優れたア
ルミニウム合金板の製造方法。 (4)溶体化処理を施して室温以上70℃以下の温度ま
で冷却した後に、室温で1日以上放置し、その後50〜
120℃の温度で1〜50時間の熱処理を、さらに行う
ことを特徴とする前記(3)に記載のプレス成形性に優
れたアルミニウム合金板の製造方法。 (5)溶体化処理を施して室温以上70℃以下の温度ま
で冷却した後に、引き続き室温以上70℃以下の温度に
保持して1〜100時間の熱処理を行うことを特徴とす
る前記(3)に記載のプレス成形性に優れたアルミニウ
ム合金板の製造方法、である。(3) After the cold rolling, the solution is subjected to a solution treatment at a temperature of 450 to 580 ° C., and then cooled from room temperature to 70 ° C. at a cooling rate of 15 ° C./s or more. ) Or the method for producing an aluminum alloy sheet excellent in press formability according to (2). (4) After performing a solution treatment and cooling to a temperature of room temperature or more and 70 ° C. or less, it is left at room temperature for one day or more,
The method for producing an aluminum alloy sheet excellent in press formability according to the above (3), further comprising performing heat treatment at a temperature of 120 ° C. for 1 to 50 hours. (5) The above-mentioned (3), wherein after performing a solution treatment and cooling to a temperature of room temperature or more and 70 ° C. or less, a heat treatment is further performed at a temperature of room temperature or more and 70 ° C. or less for 1 to 100 hours. 3. The method for producing an aluminum alloy sheet having excellent press formability described in 1. above.
【0009】[0009]
【発明の実施の形態】以下、本発明について詳細に説明
する。本発明者らは、上記の目的を達成するために、先
ずアルミニウム合金板の成形性に及ぼす材料因子につい
て種々検討した結果、合金板の(TS−YS)値(ここ
でTSは引張強さ、YSは0.2%耐力)を高めると、
プレス成形性が向上することを見出した。次に、ストレ
ッチャー−ストレイン模様の発生もなく、また時効硬化
性を有するAl−Mg−Si系合金において、プレス成
形性に及ぼす溶質原子の存在状態、合金成分および製造
条件の影響について鋭意検討した。BEST MODE FOR CARRYING OUT THE INVENTION Hereinafter, the present invention will be described in detail. The present inventors have conducted various studies on material factors affecting the formability of an aluminum alloy plate in order to achieve the above object. As a result, the (TS-YS) value of the alloy plate (where TS is the tensile strength, YS is 0.2% proof stress)
It has been found that press formability is improved. Next, in the Al-Mg-Si based alloy which has no stretcher-strain pattern and has age-hardening properties, the inventors carefully studied the influence of the presence state of solute atoms, alloy components and manufacturing conditions on press formability. .
【0010】種々検討の結果、Al−Mg−Si系合金
にCuを添加した合金において、MgおよびSiの成分
範囲およびCuの添加量を特定し、溶体化後室温近傍の
温度で形成される、溶質原子からなると考えられる低温
クラスターを形成させると130MPa以上の(TS−
YS)値が得られ、5000系合金と同等クラスの成形
性が得られること、そして140MPa以上であれば5
000系合金以上のプレス成形性が得られることを見出
した。したがって、より高い成形性を確保するためには
合金の(TS−YS)値を140以上とすることが好ま
しい。As a result of various studies, in an alloy obtained by adding Cu to an Al-Mg-Si alloy, the ranges of the components of Mg and Si and the added amount of Cu are specified, and the alloy is formed at a temperature near room temperature after solutionizing. When a low-temperature cluster considered to be composed of solute atoms is formed, (TS-
YS) value and formability equivalent to that of the 5000 series alloy is obtained.
It has been found that press formability of at least 000 series alloy can be obtained. Therefore, in order to ensure higher formability, the (TS-YS) value of the alloy is preferably set to 140 or more.
【0011】また、一般的な塗装焼付け条件である17
0から180℃程度の温度で30分間足らずの熱処理で
は、この低温クラスターは比較的安定に存在するため
に、溶質原子の過飽和固溶量を減少させ、G.P.ゾー
ンの析出を阻害してしまう。その結果、塗装焼付け処理
時には大きな強度上昇は期待できないが、合金成分およ
び製造方法を特定することによって、塗装焼付により軟
化してしまう5000系合金以上の十分な強度が得られ
ることもわかった。[0011] In addition, the general paint baking conditions of 17
In a heat treatment at a temperature of about 0 to 180 ° C. for less than 30 minutes, since this low-temperature cluster exists relatively stably, the amount of supersaturated solid solution of solute atoms is reduced. P. This hinders zone deposition. As a result, although a large increase in strength cannot be expected during the baking treatment, it was also found that by specifying the alloy components and the manufacturing method, a sufficient strength of a 5000 series alloy or more which is softened by baking paint can be obtained.
【0012】本発明における好適な成分組成範囲の限定
理由について説明する。Mg、Si、Cu、Mg、S
i、Cuは本発明の必須の基本成分であり、微細な低温
クラスターを形成して、高いプレス成形性ならびに十分
な塗装焼付硬化性を得るために含有させる。成分範囲と
しては、Mg:0.1〜0.6mass%、Si:1.
2超〜1.7mass%、Cu:0.5〜1.5mas
s%で、かつ、Mg+Si≦2mass%とした。Mg
が0.1mass%未満、Siが1.2mass%未
満、Cuが0.5mass%未満では、130MPa以
上の(TS−YS)値が得られず、十分なプレス成形性
および塗装焼付け効果性が得られない。The reason for limiting the preferred component composition range in the present invention will be described. Mg, Si, Cu, Mg, S
i and Cu are indispensable basic components of the present invention, and are contained in order to form fine low-temperature clusters and obtain high press moldability and sufficient paint bake hardenability. As the component ranges, Mg: 0.1 to 0.6 mass%, Si: 1.
More than 2 to 1.7 mass%, Cu: 0.5 to 1.5 mass
s% and Mg + Si ≦ 2 mass%. Mg
Is less than 0.1 mass%, Si is less than 1.2 mass%, and Cu is less than 0.5 mass%, a (TS-YS) value of 130 MPa or more cannot be obtained, and sufficient press moldability and paint baking effectiveness can be obtained. I can't.
【0013】また、Mgが0.6mass%超、Siが
1.7mass%超、Cuが1.5mass%超、かつ
Mg+Si>2mass%では、(TS−YS)値向上
効果は飽和するだけでなく、溶体化処理の際にMg2 S
i、Si、Al−Cu−Mg−Si系化合物等の第2相
が結晶粒界上に析出するとともに、0.2%耐力が高く
なり、ヘム曲げ性が大きく低下してしまう。本発明にお
いては、さらに必要に応じて、Ti、B、Mn、Cr、
Fe、Znのうち1種類以上を含有させてもよい。When Mg exceeds 0.6 mass%, Si exceeds 1.7 mass%, Cu exceeds 1.5 mass%, and Mg + Si> 2 mass%, the effect of improving the (TS-YS) value is not only saturated, but also , Mg 2 S during solution treatment
A second phase, such as i, Si, an Al-Cu-Mg-Si-based compound, precipitates on the crystal grain boundaries, increases the 0.2% proof stress, and greatly reduces the hem bendability. In the present invention, if necessary, Ti, B, Mn, Cr,
One or more of Fe and Zn may be contained.
【0014】TiとBは、微量添加により鋳塊の結晶粒
を微細化してプレス成形性等を改善する効果を有するの
で、Tiの含有量は0.005〜0.15mass%、
Bの含有量は0.0001〜0.05mass%の範囲
に規定するのが好ましい。それぞれの含有量がTi:
0.15mass%、B:0.05mass%を超える
と粗大な晶出物を形成し、成形性が劣化するので、それ
ぞれ0.15mass%、0.05mass%を上限と
するのが好ましい。またそれぞれの含有量がTi:0.
005mass%未満、B:0.0001mass%未
満では鋳塊の結晶粒微細化効果が十分に得られなくなっ
てしまうので、それぞれ0.005mass%、0.0
001mass%を下限とするのが好ましい。[0014] Since Ti and B have the effect of refining the crystal grains of the ingot and improving the press formability by adding a small amount, the content of Ti is 0.005 to 0.15 mass%,
It is preferable that the content of B is specified in the range of 0.0001 to 0.05 mass%. Each content is Ti:
If it exceeds 0.15 mass% and B: more than 0.05 mass%, a coarse crystallized substance is formed and the moldability deteriorates. Therefore, it is preferable that the upper limit is 0.15 mass% and 0.05 mass%, respectively. Each content is Ti: 0.
If it is less than 005 mass% and B is less than 0.0001 mass%, the effect of refining the crystal grain of the ingot cannot be sufficiently obtained.
Preferably, the lower limit is 001 mass%.
【0015】Mn、Cr、Fe、Znは強度向上および
結晶粒の微細化によってプレス成形性を向上させる効果
を有するので、それぞれMn:0.03〜0.4mas
s%、Cr:0.02〜0.15mass%、Fe:
0.03〜0.3mass%、Zn:0.03〜1%の
範囲で含有させるとよい。このうち、Mn、Cr、Fe
は、いずれも強度向上と結晶粒の微細化によりプレス成
形性を向上させる元素であり、その含有量としてMnが
0.4mass%、Crが0.15mass%、Feが
0.3mass%を超えると粗大晶出物が生成し、成形
性がかえって低下させてしまう。また、その含有量とし
てMnが0.03mass%、Crが0.02mass
%、Feが0.02mass%未満では上記の効果が十
分に得られなくなってしまうので、上述の範囲内の添加
とした。Since Mn, Cr, Fe, and Zn have the effect of improving the press formability by improving the strength and refining the crystal grains, Mn: 0.03 to 0.4mass, respectively.
s%, Cr: 0.02 to 0.15 mass%, Fe:
It is good to make it contain in the range of 0.03-0.3 mass% and Zn: 0.03-1%. Among them, Mn, Cr, Fe
Are elements that improve press formability by improving strength and refining crystal grains. When the content of Mn exceeds 0.4 mass%, the content of Cr exceeds 0.15 mass%, and the content of Fe exceeds 0.3 mass%, Coarse crystals are formed, and the moldability is rather deteriorated. Further, the content of Mn is 0.03 mass% and the content of Cr is 0.02 mass%.
% And Fe less than 0.02 mass%, the above-mentioned effects cannot be sufficiently obtained.
【0016】また、Znは、強度向上によりプレス成形
性を向上させる効果を有する。その含有量が0.03m
ass%未満では上記の効果が不十分であり、1mas
s%を超えると強度上昇が大きくなりすぎてプレス成形
性がかえって低下してしまうので、0.03〜1%の範
囲内とした。上記元素の他、通常のアルミニウム合金と
同様、不可避的不純物が含有されるが、その量は本発明
の効果を損なわない範囲であれば許容される。Zn has the effect of improving press formability by improving strength. Its content is 0.03m
If it is less than ass%, the above effect is insufficient, and 1mas
If it exceeds s%, the increase in strength becomes too large and the press formability is rather deteriorated. Therefore, it is set in the range of 0.03 to 1%. In addition to the above-mentioned elements, unavoidable impurities are contained as in the case of ordinary aluminum alloys, but the amount thereof is acceptable as long as the effects of the present invention are not impaired.
【0017】また、製造方法としては、溶体化処理後室
温まで急冷して溶質原子を過飽和に固溶させ、室温近傍
の時効により低温クラスターを形成させる方法を基本と
する。そして室温時効だけでは溶質原子の拡散が遅く短
時間では十分な強度特性が得られない場合には、室温時
効後に50〜120℃の温度範囲で引き続き熱処理を行
うことが有効である。さらに、低温クラスター形成温度
域が約70℃以下であることから、溶体化処理後に室温
以上70℃以下の低温クラスター温度範囲に急冷し、そ
の温度範囲にて時効する方法も有効である。In addition, the production method is based on a method of rapidly cooling to room temperature after the solution treatment to form a solute atom into a supersaturated solid solution and forming a low-temperature cluster by aging near room temperature. In the case where diffusion of solute atoms is slow only by aging at room temperature and sufficient strength characteristics cannot be obtained in a short time, it is effective to continue heat treatment in a temperature range of 50 to 120 ° C. after aging at room temperature. Further, since the low-temperature cluster formation temperature range is about 70 ° C. or less, a method of rapidly cooling to a low-temperature cluster temperature range of room temperature or more and 70 ° C. or less after the solution treatment and aging in that temperature range is also effective.
【0018】本発明のアルミニウム合金板の好適な製造
方法について詳しく説明する。本発明のアルミニウム合
金は、常法に従って鋳造、熱間および冷間圧延を施す
が、低温クラスターを形成させて優れた成形性を得るた
めには、冷間圧延後、450〜580℃の範囲内の温度
で溶体化処理を施して15℃/s以上の冷却速度で室温
以上70℃以下まで冷却することが有効である。上記工
程の溶体化処理条件としては、450℃以下の温度では
成形性向上ならびに塗装焼付硬化性確保(時効硬化)に
寄与する溶質原子がAl母相中に十分に固溶せずに、第
2相として析出してしまうために、成形性向上ならびに
塗装焼付硬化性の確保が得られず、またヘム曲げ性を低
下させてしまう。一方、溶体化温度が580℃を越える
と、部分溶解が生じてしまうおそれがある。そのために
溶体化処理温度は450〜580℃の範囲内とした。ま
た、上記の溶体化温度での保持については、溶質原子の
固溶が十分に行われるのならば、保持なし(溶体化処理
温度到達後、すぐに冷却)でも、ある程度の保持時間を
とっともよい。The preferred method for producing the aluminum alloy sheet of the present invention will be described in detail. The aluminum alloy of the present invention is subjected to casting, hot and cold rolling according to a conventional method. However, in order to form a low-temperature cluster and obtain excellent formability, after the cold rolling, a temperature within a range of 450 to 580 ° C. It is effective to perform a solution treatment at a temperature of not less than room temperature and not more than 70 ° C. at a cooling rate of not less than 15 ° C./s. As the solution treatment conditions in the above step, at a temperature of 450 ° C. or less, the solute atoms contributing to the improvement of the formability and ensuring the baking hardenability of coating (age hardening) do not sufficiently dissolve in the Al matrix, Because of precipitation as a phase, it is not possible to improve the formability and ensure the baking hardenability of the coating, and the hem bending property is reduced. On the other hand, if the solution temperature exceeds 580 ° C., partial melting may occur. Therefore, the solution treatment temperature was set in the range of 450 to 580 ° C. Regarding the above-mentioned holding at the solution temperature, if the solute atoms are sufficiently dissolved, even if no holding (cooling immediately after reaching the solution treatment temperature), a certain holding time is required. Good.
【0019】溶体化処理後の冷却速度を15℃/s未満
にすると、冷却中に第2相が析出し、ヘム曲げ性が低下
するとともに、溶質原子の過飽和固溶量が減少してしま
い、プレス成形性向上に有効な低温クラスター形成量が
少なくなるとともに、塗装焼付硬化能も低下してしま
う。そのため、溶体化処理温後の冷却速度は15℃/s
以上とした。また、溶体化処理後に冷却する温度範囲の
規定理由としては、70℃を越えると低温クラスターで
はなくG.P.ゾーンが形成されてしまい、室温以下で
は低温クラスターは形成されるものの、溶質原子の拡散
が遅く低温クラスターの形成に長時間を要してしまうた
めである。ここでの室温とは、概ね25℃である。If the cooling rate after the solution treatment is set to less than 15 ° C./s, the second phase precipitates during cooling, the hem bendability decreases, and the supersaturated solid solution amount of solute atoms decreases. The amount of low-temperature cluster formation effective for improving press formability is reduced, and the baking hardenability of the coating is also reduced. Therefore, the cooling rate after the solution treatment temperature is 15 ° C./s
It was above. Further, the reason for defining the temperature range for cooling after the solution treatment is that if the temperature exceeds 70 ° C., not the low-temperature cluster but G.P. P. This is because a zone is formed, and low-temperature clusters are formed below room temperature, but the diffusion of solute atoms is slow, and it takes a long time to form low-temperature clusters. The room temperature here is approximately 25 ° C.
【0020】第二に、冷間圧延後、450〜580℃の
範囲内の温度で溶体化処理を施して15℃/s以上の冷
却速度で室温まで冷却した後、室温で1日以上放置し、
その後50〜120℃の温度範囲で1〜50時間の熱処
理を施すことが、優れた成形性を得るために有効であ
る。上記工程の溶体化処理温度および冷却速度条件の設
定理由は前述した理由と同じである。溶体化後室温での
放置時間が1日未満であると、成形性向上に寄与する低
温クラスターの形成量が少なくなってしまう。Second, after cold rolling, a solution treatment is performed at a temperature in the range of 450 to 580 ° C., and the solution is cooled to room temperature at a cooling rate of 15 ° C./s or more, and then left at room temperature for 1 day or more. ,
Thereafter, it is effective to perform heat treatment in a temperature range of 50 to 120 ° C. for 1 to 50 hours to obtain excellent moldability. The reasons for setting the solution treatment temperature and cooling rate conditions in the above step are the same as those described above. If the standing time at room temperature after solution treatment is less than 1 day, the amount of low-temperature clusters that contribute to the improvement of moldability will be reduced.
【0021】また、1日以上の室温時効だけでは溶質原
子の拡散が遅く、短期間では十分な強度特性が得られ
ず、工業的な生産性の観点で問題が生じる場合がある。
その場合には、室温時効後に50〜120℃の温度範囲
で引き続き熱処理を行うことが有効である。本熱処理の
範囲の規定理由としては、50℃未満、1時間未満の処
理では、十分な強度上昇が得られず、120℃超、50
時間超では逆に強度上昇が大きくなりすぎてしまうため
である。In addition, the diffusion of solute atoms is slow only by aging at room temperature for one day or more, and sufficient strength characteristics cannot be obtained in a short period of time, which may cause a problem from the viewpoint of industrial productivity.
In that case, it is effective to continue the heat treatment in a temperature range of 50 to 120 ° C. after aging at room temperature. The reason for defining the range of this heat treatment is that if the treatment is performed at a temperature lower than 50 ° C. for less than 1 hour, a sufficient increase in strength cannot be obtained.
On the contrary, if the time is longer than the above, the increase in strength becomes too large.
【0022】第三に、溶体化処理後室温以上70℃以下
の温度まで冷却した後、引き続き室温以上70℃以下の
温度で1〜100時間の熱処理を行うことが、優れた成
形性を得るために有効でる。溶体化処理後に冷却する温
度範囲の規定理由としては、70℃を越えると低温クラ
スターではなくG.P.ゾーンが形成されてしまい、室
温以下では低温クラスターは形成されるものの、溶質の
拡散が遅く低温クラスターの形成に長時間を要してしま
うためである。Thirdly, it is preferable to cool to a temperature of from room temperature to 70 ° C. after the solution treatment and then to perform a heat treatment at a temperature of from room temperature to 70 ° C. for 1 to 100 hours to obtain excellent formability. It is effective for The reason for defining the temperature range for cooling after the solution treatment is that if the temperature exceeds 70 ° C. P. This is because zones are formed, and low-temperature clusters are formed at room temperature or lower, but the diffusion of solute is slow and the formation of low-temperature clusters takes a long time.
【0023】さらに、熱処理時間の規定理由としては、
1時間未満では低温クラスター形成量が不十分であり、
100時間以上では強度上昇が大きくなりすぎてしまう
ためである。このようにして得られたアルミニウム合金
板は、プレス成形性に優れ、かつ塗装焼付後にも500
0系合金と同等以上の十分な強度が得られる。したがっ
てこのようなアルミニウム合金板は自動車のボディシー
ト用として好適である。Further, the reason for defining the heat treatment time is as follows.
In less than one hour, the amount of low-temperature cluster formation is insufficient,
If the time is longer than 100 hours, the strength rise becomes too large. The aluminum alloy plate thus obtained has excellent press formability, and has a 500
A sufficient strength equal to or higher than that of the 0-base alloy can be obtained. Therefore, such an aluminum alloy plate is suitable for an automobile body sheet.
【0024】[0024]
【実施例】以下、本発明を実施例で説明する。 (実施例1)表1に示すような成分組成を有する合金
を、通常の方法で溶解・鋳造、圧延して板厚1mmの板
にした。そして上記圧延板に対して550℃で20秒保
持の溶体化処理を施した後室温まで30℃/sの平均冷
却速度で空冷して、アルミニウム合金板を製造した。製
造後、10日間室温に放置した後に、引張特性、成形性
(深絞り試験、球頭張出試験)を調査した。さらに塗装
焼付硬化性を評価するために、プレスにより受ける加工
に相当する2%の予ひずみを与えた後に塗装焼付処理に
相当する170℃で20分の熱処理を行い、耐力を調査
した。それらの調査結果を表2に示す。The present invention will be described below with reference to examples. (Example 1) An alloy having a component composition as shown in Table 1 was melted, cast and rolled by a usual method to form a plate having a thickness of 1 mm. The rolled sheet was subjected to a solution treatment at 550 ° C. for 20 seconds and then air-cooled to room temperature at an average cooling rate of 30 ° C./s to produce an aluminum alloy sheet. After being left at room temperature for 10 days after the production, tensile properties and moldability (deep drawing test, ball head overhang test) were examined. Further, in order to evaluate the paint bake hardenability, a heat treatment was performed at 170 ° C. for 20 minutes corresponding to the paint bake treatment after applying a 2% pre-strain corresponding to the processing received by the press, and the proof stress was examined. Table 2 shows the results of those investigations.
【0025】[0025]
【表1】 [Table 1]
【0026】本発明は5000系合金に匹敵する良好な
成形性と、5000系合金と同等以上のほぼ十分な塗装
焼付硬化性を有するアルミニウム合金板の提供を目的と
していることから、合金板の成形性能として、限界絞り
比:2.03以上、エリクセン値:10.3以上、好ま
しくは限界絞り比:2.05以上、エリクセン値:1
0.5以上を目標とした。また、塗装焼付硬化性として
は塗装焼付け後の耐力:140MPa以上を目標とし
た。The object of the present invention is to provide an aluminum alloy sheet having good formability comparable to 5000 series alloy and almost sufficient paint bake hardenability equal to or more than 5000 series alloy. As the performance, the limit aperture ratio: 2.03 or more, Erichsen value: 10.3 or more, preferably the limit aperture ratio: 2.05 or more, Erichsen value: 1
The target was 0.5 or more. Further, as the paint bake hardenability, the yield strength after paint bake was set to 140 MPa or more.
【0027】表2より、本発明のアルミニウム合金板1
〜17は、成形性に優れ、かつ塗装焼付後の強度も13
0MPa以上であることがわかる。また本発明以外の成
分を有する比較例の合金18、19では成形性が低く、
また塗装焼付硬化性も低い。一方、合金20〜25で
は、塗装焼付硬化性はあるものの、本発明成分から外れ
ているために成形性が劣っている。すなわち、本発明に
よれば、良好な成形性と十分な塗装焼付硬化性を兼ね備
えたアルミニウム合金板を製造することが可能となる。As shown in Table 2, the aluminum alloy sheet 1 of the present invention
Nos. 17 to 17 have excellent moldability and a strength after baking of 13
It turns out that it is more than 0MPa. Also, alloys 18 and 19 of comparative examples having components other than the present invention have low formability,
In addition, paint bake hardenability is low. On the other hand, alloys 20 to 25 have paint bake hardenability, but are inferior in moldability due to departure from the components of the present invention. That is, according to the present invention, it is possible to manufacture an aluminum alloy plate having both good formability and sufficient paint bake hardenability.
【0028】[0028]
【表2】 [Table 2]
【0029】(実施例2)表1の発明合金5の1mm厚
の圧延板に対して、550℃で20秒保持の溶体化処理
を施した後に冷却速度を制御して室温まで空冷した。空
冷後、室温放置の後に、引き続き熱処理を行った。溶体
化後の平均冷却速度、空冷から熱処理までの放置時間、
室温放置後の熱処理条件を表3に示す。このようにして
製造したアルミニウム合金板に対して、実施例1で行っ
たものと同様な調査を実施した。その調査結果を表4に
示す。製造条件は冷却速度が小さすぎて十分な過飽和
固溶体が得られなかったため、製造条件は溶体化後の
室温での放置が不十分であったに、良好な成形性が得ら
れなかったものである。また、製造条件は熱処理が不
十分であったために初期強度が低く、塗装焼付後の耐力
が不足してしまい、製造条件は熱処理による強度上昇
が大きすぎて、成形性が劣化してしまった。このよう
に、本発明の製造条件で処理を行ったものは上述の比較
例の製造条件に対して、成形性に優れるとともに、十分
な塗装焼付硬化量も備わっていることがわかる。Example 2 A 1 mm-thick rolled sheet of Invention Alloy 5 shown in Table 1 was subjected to a solution treatment at 550 ° C. for 20 seconds and then cooled to room temperature by controlling the cooling rate. After air-cooling, after standing at room temperature, heat treatment was continued. Average cooling rate after solution, leaving time from air cooling to heat treatment,
Table 3 shows the heat treatment conditions after standing at room temperature. Investigations similar to those performed in Example 1 were performed on the aluminum alloy plate manufactured as described above. Table 4 shows the results of the investigation. The production conditions were such that the cooling rate was too low to obtain a sufficient supersaturated solid solution, so that the production conditions were insufficient storage at room temperature after solutionization, and good moldability was not obtained. . In addition, the production conditions were such that the initial strength was low due to insufficient heat treatment, and the yield strength after coating baking was insufficient. Under the production conditions, the strength increase due to the heat treatment was too large, and the formability was deteriorated. Thus, it can be seen that the one treated under the production conditions of the present invention is excellent in moldability and has a sufficient amount of paint bake hardening as compared with the production conditions of the above-mentioned comparative example.
【0030】[0030]
【表3】 [Table 3]
【0031】[0031]
【表4】 [Table 4]
【0032】(実施例3)表1の発明合金5の1mm厚
の圧延板に対して、550℃で10秒保持の溶体化処理
を施した後に25℃/sの平均冷却速度である温度まで
空冷した。空冷後、引き続き熱処理を行った。溶体化後
の空冷温度および引き続き行う熱処理の条件を表5に示
す。このようにして製造したアルミニウム合金板に対し
て、実施例1で行ったものと同様な調査を実施した。そ
の調査結果を表6に示す。表6に示すように、本発明内
の製造条件で処理を行ったものは上述の比較例の製造条
件に対して、成形性に優れるとともに、十分な塗装焼付
硬化量も備わっていることがわかる。Example 3 A 1 mm-thick rolled sheet of invention alloy 5 in Table 1 was subjected to a solution treatment at 550 ° C. for 10 seconds and then to a temperature at an average cooling rate of 25 ° C./s. Air cooled. After air cooling, heat treatment was subsequently performed. Table 5 shows the air cooling temperature after the solution treatment and the conditions of the subsequent heat treatment. Investigations similar to those performed in Example 1 were performed on the aluminum alloy plate manufactured as described above. Table 6 shows the results of the investigation. As shown in Table 6, it can be seen that those treated under the production conditions in the present invention have excellent moldability and a sufficient amount of paint bake hardening in comparison with the production conditions of the above-mentioned comparative example. .
【0033】[0033]
【表5】 [Table 5]
【0034】[0034]
【表6】 [Table 6]
【0035】[0035]
【発明の効果】本発明によれば、成形性に優れるととも
に、十分な塗装焼付硬化性を有しており、成形性および
焼付後の耐デント性が必要とされる自動車ボディ用など
に好適なアルミニウム合金板が提供できるので、自動車
重量の軽量化に大いに寄与できる。したがって、本発明
の産業上の価値は極めて高いといえる。According to the present invention, it is excellent in moldability, has sufficient paint baking hardenability, and is suitable for an automobile body or the like that requires moldability and dent resistance after baking. Since an aluminum alloy plate can be provided, it can greatly contribute to reducing the weight of a vehicle. Therefore, it can be said that the industrial value of the present invention is extremely high.
───────────────────────────────────────────────────── フロントページの続き (51)Int.Cl.7 識別記号 FI テーマコート゛(参考) C22F 1/00 631 C22F 1/00 631Z 682 682 685 685Z 686 686A 691 691B 691C 692 692A 692B 693 693A 693B (72)発明者 高田 健 千葉県富津市新富20−1 新日本製鐵株式 会社技術開発本部内 (72)発明者 村松 俊樹 東京都墨田区錦糸1丁目2番1号 スカイ アルミニウム株式会社内 (72)発明者 野口 修 東京都墨田区錦糸1丁目2番1号 スカイ アルミニウム株式会社内──────────────────────────────────────────────────続 き Continued on the front page (51) Int.Cl. 7 Identification symbol FI Theme coat ゛ (Reference) ) Inventor Ken Takada 20-1 Shintomi, Futtsu-shi, Chiba Nippon Steel Corporation Technology Development Division (72) Inventor Toshiki Muramatsu 1-2-1 Kinshi, Sumida-ku, Tokyo Sky Aluminum Co., Ltd. (72) Invention Person Osamu Noguchi 1-2-1 Kinshi, Sumida-ku, Tokyo Sky Aluminum Co., Ltd.
Claims (5)
かつ、プレス前のTS(引張強さ)とYS(0.2%耐
力)において、(TS−YS)の値が130MPa以上
であることを特徴とするプレス成形性に優れたアルミニ
ウム合金板。1. Mass%: Mg: 0.1 to 0.6%, Si: more than 1.2 to 1.7%, Mg + Si: 2% or less, Cu: 0.5 to 1.5% And the balance consists of Al and inevitable impurities,
An aluminum alloy sheet excellent in press formability, wherein the value of (TS-YS) in TS (tensile strength) and YS (0.2% proof stress) before pressing is 130 MPa or more.
徴とする請求項1に記載のプレス成形性に優れたアルミ
ニウム合金板。2. Mass%, Ti: 0.005 to 0.15%, B: 0.0001 to 0.05%, Mn: 0.03 to 0.4%, Cr: 0.02 to 0. The press formability according to claim 1, further comprising one or more of 15%, Fe: 0.03 to 0.3%, and Zn: 0.03 to 1%. Excellent aluminum alloy plate.
溶体化処理を施した後に15℃/s以上の冷却速度で室
温以上70℃以下まで冷却することを特徴とする請求項
1または2に記載のプレス成形性に優れたアルミニウム
合金板の製造方法。3. The method according to claim 1, wherein after the cold rolling, a solution treatment is performed at a temperature of 450 to 580 ° C., and thereafter, the solution is cooled to a temperature of room temperature to 70 ° C. at a cooling rate of 15 ° C./s or more. 3. The method for producing an aluminum alloy sheet having excellent press formability according to item 2.
の温度まで冷却した後に、室温で1日以上放置し、その
後50〜120℃の温度で1〜50時間の熱処理を、さ
らに行うことを特徴とする請求項3に記載のプレス成形
性に優れたアルミニウム合金板の製造方法。4. After performing a solution treatment and cooling to a temperature of room temperature or more and 70 ° C. or less, it is left at room temperature for 1 day or more, and then further heat-treated at a temperature of 50 to 120 ° C. for 1 to 50 hours. The method for producing an aluminum alloy sheet having excellent press formability according to claim 3, characterized in that:
の温度まで冷却した後に、引き続き室温以上70℃以下
の温度に保持して1〜100時間の熱処理を行うことを
特徴とする請求項3に記載のプレス成形性に優れたアル
ミニウム合金板の製造方法。5. The method according to claim 1, wherein after performing a solution treatment and cooling to a temperature of room temperature or more and 70 ° C. or less, a heat treatment is continuously performed at a temperature of room temperature or more and 70 ° C. or less for 1 to 100 hours. 4. The method for producing an aluminum alloy sheet having excellent press formability according to 3.
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Cited By (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JP2007131881A (en) * | 2005-11-08 | 2007-05-31 | Furukawa Sky Kk | Method of producing aluminum alloy sheet for forming and aluminum alloy sheet for forming |
JP2008248297A (en) * | 2007-03-30 | 2008-10-16 | Furukawa Sky Kk | Rolled aluminum alloy sheet with excellent thermal conductivity, strength and bendability, and its manufacturing method |
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JPH04276048A (en) * | 1991-03-04 | 1992-10-01 | Furukawa Alum Co Ltd | Production of aluminum alloy sheet for forming excellent in baking hardenability |
JPH0565587A (en) * | 1991-09-05 | 1993-03-19 | Sky Alum Co Ltd | Aluminum alloy rolled sheet for forming and its production |
JPH07228957A (en) * | 1994-02-18 | 1995-08-29 | Sky Alum Co Ltd | Production of aluminum alloy sheet having excellent formability and quench-hardenability |
JPH08296011A (en) * | 1995-04-24 | 1996-11-12 | Nkk Corp | Production of aluminum alloy sheet for high speed forming excellent in baking hardenability of coating film and cold stability |
JPH10102179A (en) * | 1996-10-01 | 1998-04-21 | Nippon Steel Corp | Aluminum alloy sheet excellent in press formability and baking finish hardenability, and its production |
JPH10219382A (en) * | 1997-02-04 | 1998-08-18 | Nippon Steel Corp | Aluminum alloy sheet excellent in formability/ workability and coating/baking hardenability and its production |
JPH10259464A (en) * | 1997-03-19 | 1998-09-29 | Mitsubishi Alum Co Ltd | Production of aluminum alloy sheet for forming |
Cited By (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JP2007131881A (en) * | 2005-11-08 | 2007-05-31 | Furukawa Sky Kk | Method of producing aluminum alloy sheet for forming and aluminum alloy sheet for forming |
JP2008248297A (en) * | 2007-03-30 | 2008-10-16 | Furukawa Sky Kk | Rolled aluminum alloy sheet with excellent thermal conductivity, strength and bendability, and its manufacturing method |
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