JPS5918466B2 - Manufacturing method of Al alloy plate for packaging - Google Patents
Manufacturing method of Al alloy plate for packagingInfo
- Publication number
- JPS5918466B2 JPS5918466B2 JP249280A JP249280A JPS5918466B2 JP S5918466 B2 JPS5918466 B2 JP S5918466B2 JP 249280 A JP249280 A JP 249280A JP 249280 A JP249280 A JP 249280A JP S5918466 B2 JPS5918466 B2 JP S5918466B2
- Authority
- JP
- Japan
- Prior art keywords
- soaking
- temperature
- alloy
- hot rolling
- seizure
- 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
Links
- 238000004519 manufacturing process Methods 0.000 title claims description 8
- 238000004806 packaging method and process Methods 0.000 title claims description 8
- 229910000838 Al alloy Inorganic materials 0.000 title 1
- 239000000956 alloy Substances 0.000 claims description 37
- 229910045601 alloy Inorganic materials 0.000 claims description 37
- 238000005098 hot rolling Methods 0.000 claims description 31
- 238000002791 soaking Methods 0.000 claims description 31
- 238000000137 annealing Methods 0.000 claims description 16
- 238000005097 cold rolling Methods 0.000 claims description 10
- 229910052749 magnesium Inorganic materials 0.000 claims description 6
- 229910052804 chromium Inorganic materials 0.000 claims description 4
- 229910052802 copper Inorganic materials 0.000 claims description 4
- XEEYBQQBJWHFJM-UHFFFAOYSA-N Iron Chemical compound [Fe] XEEYBQQBJWHFJM-UHFFFAOYSA-N 0.000 description 24
- 239000002244 precipitate Substances 0.000 description 16
- 230000000694 effects Effects 0.000 description 15
- 239000000463 material Substances 0.000 description 14
- 238000010409 ironing Methods 0.000 description 10
- 238000001953 recrystallisation Methods 0.000 description 10
- 239000013078 crystal Substances 0.000 description 9
- 238000000034 method Methods 0.000 description 9
- 229910052748 manganese Inorganic materials 0.000 description 7
- 238000005275 alloying Methods 0.000 description 6
- 150000001875 compounds Chemical class 0.000 description 6
- 230000007423 decrease Effects 0.000 description 6
- 229910052742 iron Inorganic materials 0.000 description 5
- 239000000047 product Substances 0.000 description 5
- 239000000314 lubricant Substances 0.000 description 4
- 239000010687 lubricating oil Substances 0.000 description 4
- 230000015572 biosynthetic process Effects 0.000 description 3
- 238000003754 machining Methods 0.000 description 3
- 238000005096 rolling process Methods 0.000 description 3
- 239000000126 substance Substances 0.000 description 3
- 238000012360 testing method Methods 0.000 description 3
- 235000013405 beer Nutrition 0.000 description 2
- 230000007797 corrosion Effects 0.000 description 2
- 238000005260 corrosion Methods 0.000 description 2
- 230000007547 defect Effects 0.000 description 2
- 230000002542 deteriorative effect Effects 0.000 description 2
- 239000012535 impurity Substances 0.000 description 2
- 239000011159 matrix material Substances 0.000 description 2
- 230000008018 melting Effects 0.000 description 2
- 238000002844 melting Methods 0.000 description 2
- 238000001000 micrograph Methods 0.000 description 2
- 239000000203 mixture Substances 0.000 description 2
- 239000005022 packaging material Substances 0.000 description 2
- 235000014214 soft drink Nutrition 0.000 description 2
- 238000005482 strain hardening Methods 0.000 description 2
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 2
- 229910001020 Au alloy Inorganic materials 0.000 description 1
- QYEXBYZXHDUPRC-UHFFFAOYSA-N B#[Ti]#B Chemical compound B#[Ti]#B QYEXBYZXHDUPRC-UHFFFAOYSA-N 0.000 description 1
- 229910033181 TiB2 Inorganic materials 0.000 description 1
- 230000002411 adverse Effects 0.000 description 1
- 230000000573 anti-seizure effect Effects 0.000 description 1
- 238000005266 casting Methods 0.000 description 1
- 230000003247 decreasing effect Effects 0.000 description 1
- 238000002845 discoloration Methods 0.000 description 1
- 238000000635 electron micrograph Methods 0.000 description 1
- 238000005516 engineering process Methods 0.000 description 1
- 230000008020 evaporation Effects 0.000 description 1
- 238000001704 evaporation Methods 0.000 description 1
- 238000002474 experimental method Methods 0.000 description 1
- 239000012467 final product Substances 0.000 description 1
- 239000003353 gold alloy Substances 0.000 description 1
- 230000001771 impaired effect Effects 0.000 description 1
- 230000001050 lubricating effect Effects 0.000 description 1
- 238000005259 measurement Methods 0.000 description 1
- 230000003287 optical effect Effects 0.000 description 1
- 238000001556 precipitation Methods 0.000 description 1
- 238000012545 processing Methods 0.000 description 1
- 230000001105 regulatory effect Effects 0.000 description 1
- 229920006395 saturated elastomer Polymers 0.000 description 1
- 238000007790 scraping Methods 0.000 description 1
- 239000007787 solid Substances 0.000 description 1
- 230000006641 stabilisation Effects 0.000 description 1
- 238000011105 stabilization Methods 0.000 description 1
- 230000037303 wrinkles Effects 0.000 description 1
Landscapes
- Heat Treatment Of Nonferrous Metals Or Alloys (AREA)
Description
【発明の詳細な説明】
本発明は包装用A[合金板の製造方法1こ関し、特にビ
ールや清涼飲料水用罐の胴材(以下キャンボディ材とい
う)等に必要な強度及び成形性を有するA[合金板を、
高生産性のもとで製造する方法に関するものである。DETAILED DESCRIPTION OF THE INVENTION The present invention relates to a method for producing an alloy plate A for packaging, and in particular, to improve the strength and formability necessary for the body material of beer and soft drink cans (hereinafter referred to as canvas body material). A [alloy plate,
This invention relates to a manufacturing method with high productivity.
キャンボディ材等の包装用1合金板に要求される特性と
しては、
(1)深絞り性が良好であること、
(2)深絞り耳が小さいこと(結晶学的異方性が小さい
こと)、
(3)シごき加工性が良好であること、
(4)張出加工性が良好であること、
(5)ネッキング性及びフランジング性が良好であるこ
と
(6)十分な強度を有すること、
(7)耐食性が良好であること、
(8)製鑵後の外観が美麗であること、
等が挙げられる。Characteristics required for No. 1 alloy sheet for packaging such as canvas material are: (1) good deep drawability, (2) small deep drawing selvage (small crystallographic anisotropy) , (3) Good ironing workability, (4) Good stretching workability, (5) Good necking and flanging properties, and (6) Sufficient strength. (7) It has good corrosion resistance. (8) It has a beautiful appearance after iron making.
キャンボディ材としてはAA3004が最も汎用されて
いる。AA3004 is the most commonly used canvas material.
これはMn及びMgを必須成分とし他の元素を不純物と
して規制するA[合金であるが、これをキャンボディ材
として使用するとしごき加工中に焼付が発生し易い。This is an A[alloy that has Mn and Mg as essential components and other elements are regulated as impurities, but if this is used as a canvas material, seizure is likely to occur during ironing.
即ちしごき加工は製鑵工程の再絞り後1こ行なわれるも
ので、再絞りされた罐胴の側壁をしごきダイスによって
薄肉;こし、罐を高さ方向に延展して内容積を確保する
が、このときの罐壁としごきダイスとの摩擦は極めて大
きい。In other words, the ironing process is performed once after the re-drawing of the iron making process, and the side wall of the re-drawn can body is thinned by ironing dies; the inner volume is secured by stretching the can in the height direction; At this time, the friction between the can wall and the ironing die is extremely large.
その為この工程で焼付を起こし易く、これが重なると摩
擦抵抗の増大によって遂には破断に至る。Therefore, seizure is likely to occur during this process, and when this occurs, frictional resistance increases, eventually leading to breakage.
また破断しないまでも外観が著しく損なわれ、或はダイ
スの寿命が大幅に短縮される。Furthermore, even if the die does not break, the appearance is significantly impaired or the life of the die is significantly shortened.
従って焼付を防止する為に加工面の潤滑性縞める必要が
あり、通常は加工熱の冷却を兼ねて水溶性の潤滑油を使
用している。Therefore, in order to prevent seizure, it is necessary to add lubricity to the machining surface, and water-soluble lubricating oil is usually used to cool the machining heat.
しかし潤滑油の使用だけでは焼付を完全に防止し得ない
から、素材自体をも良潤滑性(又は耐焼付性)1こする
ことが望まれる。However, since seizure cannot be completely prevented by using lubricating oil alone, it is desirable that the material itself has good lubricity (or seizure resistance).
一方包装用1合金の成形性を高める為には、従来の製造
工程では、熱間圧延した板を熱間圧延後あるいは冷間圧
延途中で少なくとも1回の中間焼鈍または中間析出処理
を行なわなければ、満足な特性は得られないとされてい
る。On the other hand, in order to improve the formability of alloy 1 for packaging, in the conventional manufacturing process, the hot rolled plate must be subjected to at least one intermediate annealing or precipitation treatment after hot rolling or during cold rolling. , it is said that satisfactory characteristics cannot be obtained.
しかし中間焼鈍実施の為1こは相当の設備とエネルギー
が必要であるし、また工程数の増加によって生産性も低
下するから、中間焼鈍工程を省略することができれば、
設備面、運転経費面及び生産性等のすべての面で極めて
有利であると考えられる。However, a considerable amount of equipment and energy is required to perform intermediate annealing, and productivity also decreases due to the increase in the number of steps, so if the intermediate annealing step can be omitted,
It is considered to be extremely advantageous in terms of equipment, operating costs, productivity, etc.
本発明者等は前述の様な事情のもとで、A[合金自体の
耐焼付性を改善すると共に、中間焼鈍をしなくとも優れ
た成形性が得られる様な包装用A7合金板の製造法を確
立すべく、添加合金元素の種類や添加量及び均熱処理条
件や熱間圧延条件等1こついて種々研究を進めてきた。Under the above-mentioned circumstances, the present inventors have developed an A7 alloy sheet for packaging that improves the seizure resistance of the alloy itself and provides excellent formability without intermediate annealing. In order to establish this method, various studies have been conducted on the types and amounts of added alloying elements, soaking treatment conditions, hot rolling conditions, etc.
その結果、以下に示す如く製造条件を特定することによ
って上記の目的が兄事に達成されることを知り、絃に本
発明を完成するに至った。As a result, we found that the above objective can be achieved by specifying the manufacturing conditions as shown below, and have finally completed the present invention.
即ち本発明1こ係る包装用A[合金板の製造方法とは、
必須成分として
F e : 0.3〜0.7%(重量%二以下同じ)M
n:0.5〜2%
Mg:0.5〜2%
Si:0.05〜0,4%
を含有する他、
Cu : 0.01〜0.5%
Cr:0.01−0.5%
から選択される1種以上と
Ti:0.O1〜0.3%
B:O,OO1〜0.05%
から選択される1種以上を含み、
残部が実質的にAlからなるA[合金鋳塊を、550℃
以上の高温で24時間以内の均熱処理に付した後、終了
板厚1.8〜6rILmのものが320°C以上の終了
温度で得られる様に熱間圧延し、次いで中間焼鈍するこ
となく50%以上の冷間圧延を施すところに要旨が存在
する。That is, the present invention 1 is the method for manufacturing the packaging A [alloy plate]
Fe as an essential component: 0.3 to 0.7% (same as 2% by weight or less) M
In addition to containing n: 0.5-2% Mg: 0.5-2% Si: 0.05-0.4%, Cu: 0.01-0.5% Cr: 0.01-0.5 % or more selected from Ti: 0. O 1 to 0.3% B: O, OO 1 to 0.05% A containing one or more selected from O, OO 1 to 0.05%, the remainder being substantially Al
After being subjected to soaking treatment at a high temperature above 24 hours, hot rolling was carried out so that a final plate thickness of 1.8 to 6 rILm was obtained at a finishing temperature of 320°C or above, and then 50°C without intermediate annealing. The gist lies in performing cold rolling of % or more.
以下添加合金元素の種類、添加量及び均熱処理条件等を
定めた理由を追って本発明の構成及び作用効果を説明す
るが、下記は本発明を限定する性質のものではなく、前
・後記の趣旨1こ沿う範囲の変更はすべて本発明技術の
範噴に含まれる。The structure and effects of the present invention will be explained below, along with the reasons for determining the types of added alloying elements, the amounts added, and the soaking treatment conditions. All changes within this range are included within the scope of the technology of the present invention.
まず添加合金元素について説明する。First, the added alloying elements will be explained.
FeはMnと共1こAl Mn−Fe系の晶出物および
析出物を生成し、しごき加工時の焼付を防止すると共に
成形性を高め、製品の外観を高めるのに不可欠の元素で
ある。Together with Mn, Fe forms AlMn-Fe crystals and precipitates, and is an essential element for preventing seizure during ironing, improving formability, and improving the appearance of products.
即ち本発明者等が実験によって確認した結果では、Al
基合金におけるマトリックス中に、Al−Mn−Fe系
の比較的サイズの大きい析出物を生成させること1こよ
り、耐焼付性を大幅に向上し得ることが判明した。That is, according to the results confirmed by the inventors through experiments, Al
It has been found that seizure resistance can be significantly improved by forming relatively large-sized Al-Mn-Fe precipitates in the matrix of the base alloy.
通常の製鑵工程で水溶性潤滑剤を使用した場合、潤滑油
の濃度は水の蒸発等(こよって常時変動し、また時間の
経過と共に劣化する。When a water-soluble lubricant is used in a normal iron-making process, the concentration of the lubricant fluctuates constantly due to water evaporation, etc., and deteriorates over time.
しかも加工熱や雰囲気温度の変動1こよって潤滑油の温
度が変動し粘度も絶えず変化するから、潤滑性能の経時
変化が著しく、潤滑剤のみで焼付を完全に防止すること
はできない。Moreover, the temperature of the lubricating oil fluctuates due to fluctuations in machining heat and ambient temperature, and the viscosity of the lubricating oil also changes constantly, so the lubricating performance changes significantly over time, and seizure cannot be completely prevented using the lubricant alone.
しかし前述の如くA1合金中にA[−M n−F e系
の晶出物および析出物を生成させておくと、合金自体の
耐焼付性が向上し、潤滑剤の上記の様な性状変化のもか
かわらず焼付を効果的に防止できる。However, as mentioned above, if A[-M n-Fe system crystals and precipitates are formed in the A1 alloy, the seizure resistance of the alloy itself will improve, and the above-mentioned changes in the properties of the lubricant will occur. Despite this, seizure can be effectively prevented.
これらの効果を有意1こ発揮させる為1こは、Feを少
なくとも0.3%以上添加しなければならない。In order to exhibit these effects significantly, at least 0.3% or more of Fe must be added.
しかし0.7%を超えると耐焼付性向上効果は飽和状態
に達し、むしろA7−Mn−Fe系の巨大初晶化合物が
大量に生成して成形性が低下し、或は深絞り加工時の4
5度方向の耳が大きくなる等の弊害が著しくなる。However, when the content exceeds 0.7%, the seizure resistance improvement effect reaches a saturated state, and instead a large amount of A7-Mn-Fe-based giant primary crystal compounds are generated, resulting in decreased formability or during deep drawing. 4
Bad effects such as the ear in the 5-degree direction becoming larger become significant.
Mnは包装用AA金合金要求される強度を確保すると共
1こ、前記Al Mn−Fe系の析出物を適当なサイズ
及び量で生成させて耐焼付性を高めるのに不可欠の元素
であり、これらの効果を確保する為1こは少なくとも0
.5%以上添加する必要がある。Mn is an essential element to ensure the strength required for the AA gold alloy for packaging, as well as to generate the Al Mn-Fe type precipitates in an appropriate size and amount to improve seizure resistance. To ensure these effects, 1 is at least 0.
.. It is necessary to add 5% or more.
しかし多すぎるとFeの場合と同様巨大初晶化合物の生
成量が増大して成形性が阻害されるので、2%以下に止
めねばならない。However, if it is too large, as in the case of Fe, the amount of giant primary crystal compounds produced increases and the formability is inhibited, so it must be kept at 2% or less.
MgはMnと共1こ所定の強度を得るの1こ不可欠の元
素で、少なくとも0.5%以上添加しなければならない
。Mg, together with Mn, is an indispensable element for obtaining a certain strength, and must be added in an amount of at least 0.5%.
しかし多すぎると強度が高くなりすぎて深絞り、張出し
等の成形性が低下すると共にしごき加工時の耐焼付性が
劣化し、更には合金元素の固溶度が低下して巨大初晶化
合物が生成し易くなるので、2%以下1こ抑えるべきで
ある。However, if the amount is too high, the strength becomes too high, resulting in poor formability such as deep drawing and overhang, as well as seizure resistance during ironing, and furthermore, the solid solubility of alloying elements decreases, resulting in the formation of giant primary crystal compounds. Since it becomes easier to generate, it should be kept at 1% below 2%.
Siは、しごき加工及びその後1こ罐をポンチからホ外
す際の深絞り耳を抑制する作用がある。Si has the effect of suppressing deep drawing selvages during ironing and subsequent removal of a can from a punch.
即ちキャンボディ材1こ要求される強度を満足する為)
こは、熱間圧延後50%程度以上の冷間圧延を行なう必
要があるが、それ1こよって深絞り時ニ45度方向の耳
が発生し易くなる。In other words, to satisfy the required strength of one piece of canvas material)
This requires cold rolling of about 50% or more after hot rolling, but this tends to cause selvages in the 45 degree direction during deep drawing.
特に焼付防止の為1こFeを添加した本発明の合金では
その傾向が太きい。This tendency is particularly strong in the alloy of the present invention in which 1 piece of Fe is added to prevent seizure.
しかしSiを0.05%以上添加するとこれらの欠点を
抑制することができる。However, these defects can be suppressed by adding 0.05% or more of Si.
但し多すぎると成形性が若干悪くなるので0.4%以下
1こ止めるのがよい。However, if it is too large, the moldability will deteriorate slightly, so it is best to limit it to 0.4% or less.
Cr及びCuは何れもMnと同様の強度向上効果を発揮
するという点で同効物質であり、殊1こCuは巨大初晶
化合物生成による成形性低下を起こし難いという利点が
あるので好ましい。Both Cr and Cu are equivalent substances in that they exhibit the same strength-improving effect as Mn, and Cu is particularly preferred because it has the advantage of not easily deteriorating formability due to the formation of giant primary crystal compounds.
かかる強度向上効果はCr及び/又はCuを0.01%
以上添加することによって有効に発揮される。This strength improvement effect is achieved by adding 0.01% Cr and/or Cu.
It is effectively exhibited by adding the above.
しかしCr量が0.4%を超えるとA I −M n
−Cr系の巨大初晶化合物の生成によって成形性が阻害
され、又Cu量が0.5%を超えると耐食性が低下し包
装用材料としては適さなくなる。However, when the Cr content exceeds 0.4%, A I -M n
Formability is inhibited by the formation of -Cr-based giant primary crystal compounds, and if the amount of Cu exceeds 0.5%, corrosion resistance decreases, making it unsuitable as a packaging material.
Ti及びBは、夫々単独で或はT iB2等の形で同時
添加でき、鋳造時の内部組織を均−且つ微細1こする作
用がある。Ti and B can be added individually or simultaneously in the form of TiB2, etc., and have the effect of uniformly and finely scraping the internal structure during casting.
これらの効果を有意に発揮させる為にはTiで0.01
%以上、Bでo、oot%以上添加すべきである。In order to exhibit these effects significantly, Ti should be 0.01
% or more, B should be added in an amount of o, oot% or more.
Tiが0.3%或はBが0.05%で上記の効果は飽和
状態1こ達し、それを越えて添加することは不経請であ
るばかりでなく、巨大初晶化合物が生成し易くなって成
形性が低下するので好ましくない。At 0.3% Ti or 0.05% B, the above effects reach a saturation level of 1, and adding more than this is not only uneconomical, but also tends to generate giant primary crystal compounds. This is not preferable because the moldability deteriorates.
このほか通常のA[やA1合金に含まれる通常の不純物
元素例えばZn等1こついては、通常の範囲で含まれて
いる限り、特に悪影響を与えることはない。In addition, normal impurity elements such as Zn contained in normal A and A1 alloys do not have any particular adverse effect as long as they are contained within the normal range.
本発明のAl基合金は上記要件を満足するものでなけれ
ばならないが、更に下記の均熱条件及び熱間圧延条件を
遵守しなければ本発明の目的を達成することはできない
。Although the Al-based alloy of the present invention must satisfy the above requirements, the object of the present invention cannot be achieved unless the soaking conditions and hot rolling conditions described below are further complied with.
即ちA[基合金鋳塊の均熱処理に当っては、温度が55
0℃以上、時間が24時間以内という条件を採用しなけ
ればならない。That is, A [When soaking the base alloy ingot, the temperature is 55
The conditions must be 0°C or higher and within 24 hours.
その理由は以下1こ示す通りである。The reason for this is as shown below.
即ち本発明では、先に説明した様に所定量のFeを添加
すること;こよって耐焼付性を高めるところに大きな特
徴があるが、A[−Mn−Fe系析出物を適正なサイズ
で適正量生成させる為には均熱温度を550℃以上に設
定しなければならない。That is, the present invention has a major feature in that a predetermined amount of Fe is added as explained above; this improves seizure resistance. In order to produce a large amount, the soaking temperature must be set to 550°C or higher.
また後に詳述する如く熱間圧延終了温度を320°C以
上に設定し、熱間圧延終了時点(冷間圧延可能な温度域
で冷却されるまで)で再結晶させるので、中間焼鈍をし
なくとも良好な組織が得られる様になったという点に本
発明の重要な特徴があるが、均熱温度を550℃以上の
高温にすること1こよって、熱間圧延終了温度320℃
以上という条件を満足することが容易1こなった。In addition, as will be detailed later, the hot rolling end temperature is set at 320°C or higher, and recrystallization is performed at the end of hot rolling (until it is cooled to a temperature range that allows cold rolling), eliminating the need for intermediate annealing. An important feature of the present invention is that a good structure can be obtained in both cases, but by setting the soaking temperature to a high temperature of 550°C or higher1, the hot rolling end temperature is 320°C.
It was easy to satisfy the above conditions.
しかも均熱温度が低下しすぎると、均熱加工で微細な析
出物が生成して再結晶を抑制し、熱間圧延終了時に再結
晶させるという本発明の目的が阻害される。Moreover, if the soaking temperature is too low, fine precipitates are generated during the soaking process, suppressing recrystallization, and obstructing the purpose of the present invention of recrystallizing at the end of hot rolling.
また均熱時間は鋳塊の大きさによって適当1こ定めれば
よく、厚さ、長さ及び幅の大きいもの稈長時間(こすれ
ばよい。In addition, the soaking time may be set appropriately depending on the size of the ingot, and if the ingot is large in thickness, length, and width, it may take a long time (by rubbing).
しかし現在製造可能な最大級の鋳塊でも24時間均熱す
れば十分に均質化できる。However, even the largest ingot currently available can be sufficiently homogenized by soaking for 24 hours.
しかもこの工程で前記AA’ −Mn−Fe系析出物の
成長が進み耐焼付性が向上するが、24時間を越えて均
熱を継続しても析出物の成長は殆んど進行せず、熱エネ
ルギーが無駄に消費され且つ生産性が低下するだけであ
る。Moreover, in this step, the growth of the AA'-Mn-Fe-based precipitates progresses and the seizure resistance is improved, but even if soaking is continued for more than 24 hours, the growth of the precipitates hardly progresses. Heat energy is wasted and productivity is reduced.
上記の条件で均熱処理を行なった後は直ち1こ熱間圧延
を行なうが、その条件としては少なくとも終了板厚を1
.8〜6m’llLとし且つ終了温度を320°C以上
にしなければならない。After soaking under the above conditions, hot rolling is immediately carried out once, but the condition is that the finished plate thickness is at least 1
.. It must be 8 to 6 m'llL and the finishing temperature must be 320°C or higher.
従来から実施されているA1合金板の製造法では、熱間
圧延したA[合金板をその直後或は必要1こ応じて冷間
圧延した後中間焼鈍し、板材の機械的性質、結晶粒度及
び集合組織を調整することによって前述の様な特性を得
ていたが、本発明では上記の如く均熱から熱間圧延に至
る夫々の条件を特定することによって、中間焼鈍の省略
が可能になった。In the conventional manufacturing method of A1 alloy sheet, the hot-rolled A alloy sheet is subjected to intermediate annealing immediately after or after cold rolling as necessary, and the mechanical properties, grain size and The properties described above were obtained by adjusting the texture, but in the present invention, by specifying each condition from soaking to hot rolling as described above, it has become possible to omit intermediate annealing. .
本発明における重大な特徴である熱間圧延終了時の再結
晶について、更に詳細な説明を加える。A more detailed explanation will be given of recrystallization at the end of hot rolling, which is an important feature of the present invention.
内部歪を発生させる元素(Mn、Mg等)の少ないA1
合金或は純Alの場合、熱間圧延終了時に再結晶を完了
させる為]こは熱間圧延を非常な高温で行なわねばなら
ない。A1 with less elements that cause internal strain (Mn, Mg, etc.)
In the case of alloys or pure Al, hot rolling must be carried out at a very high temperature in order to complete recrystallization at the end of hot rolling.
しかし終了板厚を薄くする程温度は低下するので、良好
な再結晶組織を有する薄肉の熱間圧延板を得ることは困
難である。However, since the temperature decreases as the final plate thickness decreases, it is difficult to obtain a thin hot rolled plate having a good recrystallized structure.
即ち熱間圧延終了時に効果的な再結晶を行なう為(こは
、再結晶を引き起こす為の駆動歪とその歪を解放する為
の熱エネルギーが不可欠であると考えられる。That is, in order to carry out effective recrystallization at the end of hot rolling, it is thought that driving strain to cause recrystallization and thermal energy to release the strain are essential.
この点本発明では、A1合金成分中に所定量のMg及び
Mnを含有させ、熱間圧延中の内部歪を大きくしている
から、これが駆動歪になり、比較的少ない熱エネルギー
で再結晶を行なうことができる。In this regard, in the present invention, a predetermined amount of Mg and Mn is contained in the A1 alloy component to increase internal strain during hot rolling, so this becomes a driving strain and recrystallization can be performed with relatively little thermal energy. can be done.
即ち格別の中間焼鈍を行なわなくとも熱間圧延の段階で
十分な再結晶が可能になる。That is, sufficient recrystallization is possible at the hot rolling stage without special intermediate annealing.
しかしこの場合でも最少限の熱エネルギーは必要であり
、かかる観点から熱間圧延終了温度は320℃以上に定
めた。However, even in this case, a minimum amount of thermal energy is required, and from this point of view, the hot rolling end temperature was set at 320° C. or higher.
また終了板厚1こついては、厚肉なる程終了温度を高温
・一定に維持し易くなるが、圧延による内部歪が少なく
なって前記駆動型が小さくなり、熱間圧延段階で再結晶
を完結させることが困難になる。In addition, when the finished plate thickness is 1, the thicker the plate, the easier it is to maintain the finished temperature at a high and constant level, but the internal strain caused by rolling becomes smaller, the drive die becomes smaller, and recrystallization is completed in the hot rolling stage. things become difficult.
しかもこれを通常のキャンボディ材に適した板厚まで冷
間圧延すると、加工硬化)こよって強度が極端に高くな
り、最終製品板の成形性が低下する。Moreover, when this is cold rolled to a thickness suitable for ordinary canvas body materials, the strength becomes extremely high due to work hardening (work hardening), and the formability of the final product sheet decreases.
従ってこれらの障害が実質上現われない様(こする為に
、熱間圧延終了時の板厚を6に以下とした。Therefore, in order to prevent these defects from appearing, the plate thickness at the end of hot rolling was set to 6 or less.
一方終了板厚す月、 8 mm未満になると、終了温度
を320℃以上にすることが困難になる。On the other hand, if the final plate thickness is less than 8 mm, it becomes difficult to raise the final temperature to 320°C or higher.
殊1こ熱間圧延材として純1’の様な高融点の材料を使
用する場合は、均熱温度を高くできるので、これに続く
熱間圧延の開始温度及び終了温度も高くできるが、本発
明で使用する合金の様)こMn、Mg、Fe等の合金元
素を相当量含むものでは融点が低いから、均熱温度を比
較的低温1こしなければならず、熱間圧延の開始及び終
了温度も低下してくる。In particular, when using a material with a high melting point such as pure 1' as the hot-rolled material, the soaking temperature can be increased, so the start and end temperatures of the subsequent hot rolling can also be increased. Since the melting point of alloys containing a considerable amount of alloying elements such as Mn, Mg, and Fe (such as the alloy used in the invention) is low, the soaking temperature must be kept relatively low, and the start and end of hot rolling must be kept at a relatively low temperature. The temperature will also drop.
その為熱間圧延終了板厚を薄くすると圧延終了温度を3
20℃以上に保持することが困難になり、完全に再結晶
した熱間圧延板は得られ難くなる。Therefore, if the plate thickness at the end of hot rolling is reduced, the temperature at the end of rolling can be reduced by 3.
It becomes difficult to maintain the temperature at 20° C. or higher, and it becomes difficult to obtain a completely recrystallized hot rolled sheet.
従って本発明では、適正な圧延終了温度を確保する為に
、終了板厚を1.8r/を以上に限定した。Therefore, in the present invention, the finished plate thickness is limited to 1.8 r/ or more in order to ensure an appropriate rolling finish temperature.
上記の均熱及び熱間圧延条件を採用すること1こより、
熱間圧延終了時に十分な再結晶組織を有する圧延板が得
られ、その後50%以上の冷間圧延を施すこと1こよっ
て、キャンボディ材として必要な強度を有するA1合金
板が得られる。By adopting the above soaking and hot rolling conditions,
A rolled sheet having a sufficient recrystallized structure is obtained at the end of hot rolling, and then cold rolling is performed by 50% or more.1 Thereby, an A1 alloy sheet having the strength required as a canvas body material is obtained.
尚この仕上げ冷間圧延の後に、必要であれば安定化焼鈍
(100〜150℃程度で1時間以内)を施し、機械的
性質の調整等を図ることも可能である。After this final cold rolling, if necessary, stabilization annealing (at about 100 to 150° C. for less than 1 hour) can be performed to adjust the mechanical properties.
この様に本発明では熱間圧延後の中間焼鈍を省略できる
が、これは耐焼付性を高めまた美麗な製品を得る上でも
重要な意味がある。In this way, in the present invention, intermediate annealing after hot rolling can be omitted, which has an important meaning in improving seizure resistance and obtaining a beautiful product.
即ち熱間圧延の後中間焼鈍を行なうと、Mgが板材表面
に拡散浸出し更には酸化されてMgOとなり、前記Al
−Mn Fe系析出物によって折角付与された耐焼付
性が減殺され、更には板材表面が黒色を帯びて美感が低
下する。That is, when intermediate annealing is performed after hot rolling, Mg diffuses into the surface of the plate material and is further oxidized to become MgO.
-Mn The Fe-based precipitates reduce the anti-seizure property that has been so painstakingly imparted, and furthermore, the surface of the plate material takes on a black tinge, deteriorating its aesthetic appearance.
しかし本発明では中間焼鈍を行なう必要がないから上記
の様な障害を起こす恐れも全くない。However, in the present invention, there is no need to perform intermediate annealing, so there is no risk of causing the above-mentioned problems.
本発明は概略以上の様に構成されており、その効果を要
約すれば下記の通りである。The present invention is roughly constructed as described above, and its effects can be summarized as follows.
■ 合金元素としてMn及びFeを含有させると共に均
熱条件を特定すること1こよって、Alマトリックス中
1こAl−Mn−Feの系晶出物および析出物を生成さ
せ、合金板目体1こ自己潤滑性を与えたから、特にしご
き加工時の焼付現象を可及的に防止できる。■ Including Mn and Fe as alloying elements and specifying the soaking conditions1.Thus, Al-Mn-Fe system crystals and precipitates are formed in the Al matrix, and one alloy plate is formed. Since it has self-lubricating properties, it is possible to prevent seizure as much as possible, especially during ironing.
従って加工時の変色が抑制されて美麗な製品が得られ、
更1こはダイスの摩耗も大幅に抑制される。Therefore, discoloration during processing is suppressed and beautiful products can be obtained.
Furthermore, die wear is also significantly suppressed.
■ 中間焼鈍の省略を可能]こしたから、上記■の耐焼
付性向上効果をそのまま維持できる。(2) Intermediate annealing can be omitted], so the seizing resistance improvement effect described in (2) above can be maintained as is.
更には中間焼鈍1こ要する設備、熱エネルギーが不要1
こなり、また工程数の減少によって生産性も向上する。Furthermore, no equipment or thermal energy is required for intermediate annealing.
This also improves productivity by reducing the number of steps.
■ 得られる製品は優れた強度を有すると共1こ、優れ
た成形性を発揮する。■ The resulting product has excellent strength and also exhibits excellent moldability.
従ってビールや清涼飲料水用のキャンボディ材をはじめ
として、各種の包装用1こ幅広く使用できる。Therefore, it can be used in a wide variety of packaging materials, including canvas materials for beer and soft drinks.
次に本発明の実施例を示す。Next, examples of the present invention will be shown.
実施例 l
第1表1と示す成分組成のA[合金鋳塊(厚さ:500
mm)を590°Cで6時間均熱処理した後、終了板厚
2.5 am、終了温度330℃で熱間圧延し、更に0
.4 arn厚まで冷間圧延して得たA1合金の機械的
性質及びしごき加工時の耐焼付性を調べた。Example l A [alloy ingot (thickness: 500
mm) was soaked at 590°C for 6 hours, then hot rolled at a final thickness of 2.5 am and a final temperature of 330°C, and then
.. The mechanical properties of the A1 alloy obtained by cold rolling to a thickness of 4 arn and the seizure resistance during ironing were investigated.
結果を第2,3表に示す。The results are shown in Tables 2 and 3.
但し耐焼付性試験では、各合金板表面を脱脂した後試験
に供した。However, in the seizure resistance test, the surface of each alloy plate was degreased before being subjected to the test.
○:焼付(なし)■:焼付(小)△:焼
付(中)×:焼付(犬)
第1〜3表からも明らかな様1こ、Feの添加量を変え
ても機械的性質には殆んど差が認められない。○: Seizure (no) ■: Seizure (small) △: Seize (medium) Almost no difference is recognized.
しかし耐焼付性はFe量によって著しく影響され、0.
3%未満(合金A)では極めて劣悪であるのに対し、本
発明で規定するFe量を満足する合金(合金B及びC)
の耐焼付性は極めて良好である。However, the seizure resistance is significantly affected by the amount of Fe;
If it is less than 3% (alloy A), it is extremely poor, whereas alloys that satisfy the Fe content specified in the present invention (alloys B and C)
The seizure resistance is extremely good.
また第1表に示した合金N及びBを用い、均熱条件を5
40℃×4時間に変更した他は上記と同様1こして0.
4 am厚の合金板を製造し、耐焼付性試験を行なった
。Also, using alloys N and B shown in Table 1, soaking conditions were set to 5.
Same as above except that the temperature was changed to 40°C x 4 hours.
An alloy plate with a thickness of 4 am was manufactured and subjected to a seizure resistance test.
結果を第4表に示す。但し均熱条件590℃×6時間の
ときの結果を併記した。The results are shown in Table 4. However, the results under soaking conditions of 590° C. x 6 hours are also shown.
(○、@、△、×:同前)
第4表の結果からも明らかな様1こ、Fe含有量が本発
明の要件を満たしていても、均熱温度が550℃未満で
は耐焼付性改善効果が不十分であり、また均熱温度が本
発明の要件を満たしていても、Fe量が0.3%未満で
は耐焼付性は殆んど向上しない。(○, @, △, ×: Same as above) As is clear from the results in Table 4, even if the Fe content satisfies the requirements of the present invention, the seizure resistance is poor when the soaking temperature is lower than 550°C. The improvement effect is insufficient, and even if the soaking temperature satisfies the requirements of the present invention, if the Fe amount is less than 0.3%, the seizure resistance will hardly improve.
実施例 2
第5表に示す成分組成のAA合金鋳塊(厚さ1500m
m)を590℃で6時間均熱処理した後、終了板厚を2
.5 rnm一定とし、終了温度が330℃、315°
C又は300℃となる様に熱間圧延を行ない、夫々(こ
ついて0.4 rnrrt厚まで冷間圧延を行なった。Example 2 An AA alloy ingot having the composition shown in Table 5 (thickness: 1500 m)
m) was soaked at 590℃ for 6 hours, and the final plate thickness was reduced to 2.
.. 5 rnm constant, end temperature 330°C, 315°
C or 300° C., and then cold rolled to a thickness of 0.4 rnrrt.
得られた圧延板の機械的性質及び絞り加工1こおける耳
率を測定した。The mechanical properties of the obtained rolled plate and the selvage ratio after one drawing process were measured.
但し耳率の測定は下記の通りとした。However, the ear rate was measured as follows.
ポンチ径 :33門 絞り率 二0.6 クリアランス:25% しわ押え荷重:100kg 絞り速度 :13rIt11L/秒 結果を第6,7表に示す。 Punch diameter: 33 guns Aperture ratio 20.6 Clearance: 25% Wrinkle presser load: 100kg Aperture speed: 13rIt11L/sec The results are shown in Tables 6 and 7.
第5〜7表からも明らかな様:こ、熱間圧延終了温度を
330°C1こ設定した場合、得られた製品の絞り加工
時1こおける耳率は尾部、中央部、頭部共にほぼ均一で
且つ小さいが、終了温度を320°C未満(こすると、
圧延コイル長手方向の耳率の差が大きく且つ絶対値も大
きくなる。As is clear from Tables 5 to 7: When the hot rolling end temperature is set at 330°C, the selvedge ratio in the drawing process of the obtained product is almost the same for the tail, center, and head. Uniform and small, but with a finishing temperature of less than 320°C (by rubbing,
The difference in the selvage ratio in the longitudinal direction of the rolled coil is large and the absolute value is also large.
また第1図は、熱間圧延後の各合金板の平行方向断面顕
微鏡写真で、終了温度が320°C未満では再結晶が完
了している。Moreover, FIG. 1 is a parallel cross-sectional micrograph of each alloy plate after hot rolling, and recrystallization is completed when the finishing temperature is less than 320°C.
実施例 3
第8表1と示す成分組成の大型A1合金鋳塊より50X
75X1001rL1?Lの小型鋳塊を切り出し、異な
る温度で均熱処理を施した後、水冷して均熱直後の状態
をそのまま保存し、夫々の内部組織を光学顕微鏡によっ
て観察した。Example 3 50X from a large A1 alloy ingot with the composition shown in Table 8
75X1001rL1? Small ingots of L were cut out, subjected to soaking treatment at different temperatures, cooled with water, and stored in the state immediately after soaking, and the internal structure of each ingot was observed using an optical microscope.
結果を第2図)こ示す。第2図からも明らかな様(こ、
鋳造のままでは晶出物はみられるものの析出物は生成し
ていない。The results are shown in Figure 2). As is clear from Figure 2 (this,
Although crystallized substances are observed in the as-cast state, no precipitates are formed.
しかし均熱処理を施すと析出物が生成し、また均熱温度
が高い程近出物のサイズは大きくなっている。However, when soaking is performed, precipitates are formed, and the higher the soaking temperature, the larger the size of the precipitates.
尚450℃×4時間の均熱処理の場合、写真では析出物
が生成していない様に見えるが、第3図の電子顕微鏡写
真からも明らかな様に実際は非常1こ微細な析出物が多
量に生成している。In the case of soaking treatment at 450℃ for 4 hours, it appears that no precipitates were formed in the photograph, but as is clear from the electron micrograph in Figure 3, in reality, a large amount of very fine precipitates were formed. is being generated.
但し明細書本文でも説明した様に、析出物は比較的サイ
ズが大きくなれば耐焼付性の向上(こ寄与しないから、
その為には550℃以上の均熱温度を採用する必要があ
る。However, as explained in the main text of the specification, if the precipitates are relatively large in size, they will not improve the seizure resistance (because they will not contribute).
For this purpose, it is necessary to adopt a soaking temperature of 550°C or higher.
尚これらの晶出物及び析出物は、均熱後の鋳塊の段階で
は不均一な分布をしているが、その後に行なわれる熱間
圧延及び冷間圧延により均一な分布となる。These crystallized substances and precipitates are non-uniformly distributed in the ingot after soaking, but become uniformly distributed by the subsequent hot rolling and cold rolling.
第1〜3図はA1合金の内部組織を示す図面代用顕微鏡
写真である。Figures 1 to 3 are micrographs substituted for drawings showing the internal structure of the A1 alloy.
Claims (1)
n:0.5〜2% Mg:0.5〜2% Si:0.05〜0.4% を必須成分として含有する他 Cu : 0.01〜0.5% Cr : 0.01〜0.5% から選択される1種以上と Ti:0.01〜0.3% B:0.OO1〜0.05% から選択される1種以上を含み、残部が実質的にA[か
らなるA1合金鋳塊を、550℃以上の高温で24時間
以内の均熱処理(こ付した後、終了板厚1.8〜6rI
LrILのものが320℃以上の終了温度で得られる様
1こ熱間圧延し、次いで中間焼鈍することなく50%以
上の冷間延を施すことを特徴とする包装用A1合金板の
製造方法。[Claims] I Fe: 0.3 to 0.7% (same as 2% by weight or less) M
n: 0.5-2% Mg: 0.5-2% Si: 0.05-0.4% Cu: 0.01-0.5% Cr: 0.01-0 .5% and one or more selected from Ti: 0.01-0.3% B: 0.5%. An A1 alloy ingot containing one or more selected from 1 to 0.05% of OO, with the remainder consisting essentially of A, is subjected to soaking treatment (after soaking and finishing) at a high temperature of 550°C or higher for within 24 hours. Plate thickness 1.8~6rI
A method for producing an A1 alloy sheet for packaging, characterized by hot rolling one time so that LrIL is obtained at a finishing temperature of 320° C. or more, and then cold rolling by 50% or more without intermediate annealing.
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP249280A JPS5918466B2 (en) | 1980-01-11 | 1980-01-11 | Manufacturing method of Al alloy plate for packaging |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP249280A JPS5918466B2 (en) | 1980-01-11 | 1980-01-11 | Manufacturing method of Al alloy plate for packaging |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| JPS56102562A JPS56102562A (en) | 1981-08-17 |
| JPS5918466B2 true JPS5918466B2 (en) | 1984-04-27 |
Family
ID=11530853
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP249280A Expired JPS5918466B2 (en) | 1980-01-11 | 1980-01-11 | Manufacturing method of Al alloy plate for packaging |
Country Status (1)
| Country | Link |
|---|---|
| JP (1) | JPS5918466B2 (en) |
Families Citing this family (10)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JPS58224142A (en) * | 1982-06-22 | 1983-12-26 | Sumitomo Light Metal Ind Ltd | Aluminum alloy plate with superior formability and its manufacture |
| JPS59179768A (en) * | 1983-03-31 | 1984-10-12 | Sumitomo Light Metal Ind Ltd | Production of aluminum or aluminum alloy plate |
| JPS61110744A (en) * | 1984-11-02 | 1986-05-29 | Kobe Steel Ltd | Al alloy plate for packing and its manufacture |
| JPS62218540A (en) * | 1986-03-19 | 1987-09-25 | Furukawa Alum Co Ltd | Al alloy for receiver tank |
| JPS62230945A (en) * | 1986-03-31 | 1987-10-09 | Sumitomo Light Metal Ind Ltd | Aluminum alloy sheet for package excellent in corrosion resistance and its production |
| JPH0826428B2 (en) * | 1987-08-21 | 1996-03-13 | 古河電気工業株式会社 | Aluminum alloy plate material for forming |
| JPH0225539A (en) * | 1988-07-13 | 1990-01-29 | Sky Alum Co Ltd | Aluminum alloy hard plate for forming and its production |
| US6955785B2 (en) * | 2002-09-05 | 2005-10-18 | Honda Giken Kogyo Kabushiki Kaisha | Aluminum alloy for rapidly cooled welding and welding method therefor |
| CN103008342B (en) * | 2012-12-27 | 2015-06-17 | 亚洲铝业(中国)有限公司 | Production method of 5052-H32 aluminum alloy plate-strip |
| CN114622114B (en) * | 2022-03-16 | 2022-12-09 | 诺文(新会)合金材料有限公司 | Method for manufacturing special aluminum sheet |
-
1980
- 1980-01-11 JP JP249280A patent/JPS5918466B2/en not_active Expired
Also Published As
| Publication number | Publication date |
|---|---|
| JPS56102562A (en) | 1981-08-17 |
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