JPH0545653B2 - - Google Patents
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- JPH0545653B2 JPH0545653B2 JP60114581A JP11458185A JPH0545653B2 JP H0545653 B2 JPH0545653 B2 JP H0545653B2 JP 60114581 A JP60114581 A JP 60114581A JP 11458185 A JP11458185 A JP 11458185A JP H0545653 B2 JPH0545653 B2 JP H0545653B2
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Description
産業上の利用分野
この発明は、ぶりき用の原板あるいはテインフ
リー鋼板(以下TFSと記す)用の原板の如き、
表面処理用原板の製造方法に関し、特に連続焼鈍
法を適用して表面処理用原板を調質度T4とT5
に作り分ける方法に関するものである。
従来の技術
周知のようにぶりき原板は、鋼素材に熱間圧延
および冷間圧延を施して得られた冷延鋼板に焼な
ましを施し、さらに必要に応じて調質圧延を行な
つて、必要な硬さを得るのが通常である。このよ
うなぶりき原板の調質度は、JIS G3303によつて
次のように規定されている。すなわち軟質なもの
から順に調質度T1からT6まで区分され、それ
ぞれ硬さ目標値としてロツクウエル硬さ
(HR30T)で調質度T1が49±3、T2が53±
3、T3が57±3、T4が61±3、T5が65±
3、T6が70±3とされている。
このような各調質度のぶりき原板のうち、調質
度T1からT3までのいわゆる軟質板はその焼な
まし工程に箱焼鈍法を適用して製造し、また調質
度T4〜T6の硬質板は連続焼鈍法を適用して製
造するのが通常である。
ところで調質度T4〜T6の連続焼鈍法によつ
て得られるぶりき原板の各調質度ごとの板の作り
分け、特に調質度T4の原板と調質度T5の原板
との作り分けは、従来は鋼素材の化学成分のみを
変えることによつて行なうのが通常であつた。す
なわち調質度T4の原板は通常の底炭素鋼を素材
とし、一方調質度T5の原板はNやCを添加して
硬質化した銅を素材として用い、いずれの場合も
熱延温度、冷間圧延条件、連続焼鈍証言、調質圧
延圧下率等は調質度によつて変えないのが一般的
であつた。このように鋼素材の化学成分のみの変
化によつて調質度T4,T5の原板を作り分けて
いた理由としては、先ず第1には、化学成分を変
化させること自体は技術的に容易であることが挙
げられ、また第2には、製造条件を変えることが
設備的に困難とされ、またそのための技術的基盤
が確立していなかつたことが考えられる。
しかるに最近ではぶりき原板需要者の要求が従
来より一層厳しくなり、正確に目標値に適合した
硬さを有することが要求されるようになつている
が、素材の化学成分のみを変化させる従来の一般
的な方法では需要者の要求を満足させ得ない場合
も生じている。また一方、原板の製造方法自体に
対しても、より効率的な製造方法の確立が望まれ
ているが、特に前述のような調質度T4,T5の
原板は、その生産量が多く、またその用途も類似
しているにもかかわらず、従来は化学成分を異な
らしめるために製鋼段階からそれぞれ別々に取扱
わなければならず、工程管理が極めて煩雑となつ
ており、その改善が望まれている。そこで鋼素材
自体の化学成分は同一とし、最終工程に近い焼鈍
工程あるいは調節圧延工程の条件を変えることに
よつて調質度T4の原板とT5の原板とを作り分
けるための方法が従来からいくつか提案されてい
る。
例えば特開昭57−70227号公報には、焼鈍時の
冷却速度のみを変えて調質度を制御する方法が提
案されている。また一方、特開昭55−114401号公
報においては、直径50〜300mmのワークロールを
具備する特殊な調質圧延機を用いて調質圧延の圧
下率を高圧下とすることにより、T1〜T6まで
の全調質度の板を同一素材から作り分ける方法も
提案されている。
発明が解決すべき問題点
異なる調質度のぶりき原板、特に調質度T4の
原板とT5の原板を効率的に作り分けるために
は、鋼素材の成分は同一とし、原板製造過程の最
終工程に近い工程での条件を制御して調質度を制
御することが好ましく、そのための方法としては
既に述べたような特開昭57−70227号公報記載の
方法や、特開昭55−114401号公報記載の方法が提
案されている。しかしながらこれらの提案の方法
はいずれも実用的なものではなく、また方法によ
つては別の新たな問題も発生する。
すなわち特開昭57−70227号公報記載の方法は、
通常使用されている底炭素Alキルド鋼またはリ
ムド鋼を素材とし、それを熱間圧延および冷間圧
延後、連続焼鈍するに際して均熱後の室温までの
冷却速度を大きく変化させることによつて、調質
度T4の板とT5の板とを作り分けようとするも
のであり、この公報には、調質度T4の板を得る
ためには冷却速度を5〜20℃/秒とし、また調質
度T5の板を得るためには冷却速度を100〜300
℃/秒とすることが適当である旨記載されてい
る。なお連続焼鈍後の調質圧延については、調質
度T4,T5のいずれの場合も同一の圧下率1%
を適用している。このように焼鈍後の冷却速度の
制御のみによつて硬さを変化させようとする試み
は、上記公報に限らず、従来から多数提案されて
いるが、前述のように調質度T4とT5とを作り
分けるためには冷却速度の変化幅を著しく広くし
なければならず、そのため連続焼鈍設備の長大化
と操業コストの増大を招くため、現実に適用する
ことは困難であつた。
一方、連続焼鈍後の調質圧延における圧下率を
変化させて調質度を制御する特開昭55−114401号
公報記載の方法では、同公報中の実施例によれ
ば、調質度T4の板とT5の板とを作り分けるた
めには調質圧延圧下率を大きく変えなければなら
ない。特に調質度T5の板を製造するためには圧
下率を2.7〜2.8%と極端な高圧下としなければな
らない。このような高圧下を得るためには、同公
報中にも詳細に説明されているように小径の特殊
なワークロールを必要とし、そのため通常の調質
圧延機の適用は不可能であるから、既存のライン
では製造することができない。また前述のように
調質圧延圧下率を大幅に変化させるためには、そ
れに伴なつて冷間圧延仕上り板厚の変更も必要と
なるため、生産効率が大きく低下してしまう問題
が生じる。さらに、圧下率2.7〜2.8%にも及ぶ高
圧下とした場合、加工性が乏しくなつて溶接部等
で割れが発生し易くなるなどの問題も招く。
以上のように、従来提案されている方法では、
それを現実に適用して、高い生産効率で調質度T
4とT5の原板を作り分けるには不適当であつ
た。
この発明は以上の事情を背景としてなされたも
ので、前述のような諸問題を招くことなく、同一
の化学成分を含有する鋼素材から調質度T4のぶ
りき原板あるいはTFS原板等の表面処理用原板
と、調質度T5の表面処理用原板を効率的に作り
分ける方法を提供することを目的とするものであ
る。
問題点を解決するための手段
本発明者等は上述の目的を達成するべく種々実
験・検討を重ねた結果、特定の化学成分の鋼を素
材とし、その化学成分条件と、熱間圧延条件、連
続焼鈍条件、調質圧延圧下率を適切に組合せるこ
とによつて、従来から提案されている各方法の如
き大幅な条件変更を伴なうことなく、効率良くか
つ正確に調質度T4の表面処理用原板と調質度T
5の表面処理用原板とを作り分け得ることを見出
し、この発明をなすに至つたのである。
すなわちこの発明の方法は、C 0.02〜006%
(重量%、以下同じ)、N 0.004〜0.01%、Mn
0.1〜0.4%、Al 0.01〜0.04%を含有し、かつN量
とAl量との比N(%)/Al(%)が0.15以上とさ
れ、残部がFeおよび不可避的不純物よりなる鋼
を素材とし、熱延板巻取温度600℃以下となるよ
うに熱間圧延した後冷間圧延し、さらに連続焼鈍
により再結晶温度以上、Al変態点以下の温度に
均熱して冷却し、その後調質圧延を行なつて、調
質度T4もしくはT5の表面処理用原板を製造す
るにあたり、前記連続焼鈍における均熱後の冷却
過程における500〜400℃の間の平均冷却速度と、
調質圧延における圧下率とを、最終的に得るべき
調質度T4もしくはT5に応じて次の(イ)、(ロ)のう
ちのいずれかの条件に設定することによつて、調
質度T4の表面処理用原板と調質度T5の表面処
理用原板を作り分けることを特徴とするものであ
る。
(イ) 調質度T4の場合:
平均冷却速度55℃/sec以下、調質圧延圧下
率1.0〜2.0%
(ロ) 調質度T5の場合:
平均冷却速度65℃/sec以上、調質圧延圧下
率1.5〜2.5%。
発明の具体的説明
先ずこの発明をなすに至る基礎となつた実験結
果について説明する。
第1表に示すように2種の異なる化学成分を有
する低炭素Alキルド鋼を通常の工程で熱間圧延
および冷間圧延して、板厚0.25mmの冷延板を得
た。各冷延板に対し、第1図のA,Bに示す2種
のパターンのヒートサイクルで焼なまし熱処理を
程し、さらに小型圧延機にて0.1〜3.5%程度の圧
延率の調質圧延を施した。次いで250℃×3秒間
の溶錫相当処理を施した後、ロツクウエル硬さ
(HR30T)を測定した。その結果を第2図に示
す。
この実験結果から、鋼成分とヒートサイクルパ
ターンの変化(冷却速度の変化)によりそれぞれ
の硬さが異なるのみならず、硬さの調質圧延率依
存性も大きく変化することが判明した。すなわち
例えば鋼1の場合にはヒートサイクルパターンの
変化(冷却速度の変化)による硬さの変化が比較
的小さく、しかも調質圧延率の変化による硬さの
変化も比較的小さい。そのため鋼1の場合は、調
質度T5の硬さを得るためには調質圧延率を3.0
%以上と高圧下としなければならず、通常の調質
圧延機での圧延は極めて困難であることがわか
る。一方鋼2では、ヒートサイクル感受性が大き
く、特に徐冷した場合には単に硬さが小さいのみ
ならず調質圧延率依存性が比較的小さく、調質圧
延率の増大に伴なう硬さの上昇傾向がさほど大き
くないのに対し、急冷した場合には調質圧延率依
存性が著しく大きくなり、調質圧延率の増大に伴
なつて硬さが急激に高くなる。
したがつてこのような実験結果から、鋼成分を
適切に設定すれば、ヒートサイクル(冷却速度)
と調質圧延率を適切に組み合せることによつて目
標硬さに正確に合致した調質度T4と調質度T5
の板を効率良く作り分け得ることが予想される。
そしてこれを実現するためには、適切な成分系
と、それに適したヒートサイクルの組み合せを見
出すことが不可欠であり、さらに最適な調質圧延
の条件を見出すことも不可欠である。そこでこれ
らの条件を明らかにするために、さらに詳細な実
験を行なつた結果、既に述べたようなこの発明の
条件が必要であることが判明し、この発明をなす
に至つたのである。
次にこの発明における各条件を実験結果に基い
て説明する。
先ず連続焼鈍工程において焼鈍温度に均熱保持
後の冷却速度については、500〜400℃の間の冷却
速度を、調質度T4を得る場合は55℃/sec以下、
調質度T5を得る場合は65℃/sec以上とする必
要がある。このように冷却速度を制御する範囲を
500〜400℃の間と規定したのは、次のような実験
結果に基づく。
すなわち第1表の鋼2の熱間圧延、冷間圧延後
の板厚0.25mmの冷延板について、第3図に示すよ
うに680℃で5秒間均熱し、直ちに100℃以下の温
度まで連続して25℃/secの冷却速度で冷却した
場合と、その25℃/secの冷却速度での冷却過程
中途の種々の温度Tから70℃/secで急冷する実
験を行ない、100℃以下の温度まで35℃/secで徐
冷した場合に対する、各温度Tから70℃/secで
急冷した場合の鋼中のC固溶量の差を調べた。そ
の結果を第4図に示す。第4図の結果から、冷却
速度を35℃/secの徐冷から70℃/secの急冷へ変
化させた場合のC固溶量の差が大きいのは、冷却
速度変更温度Tが400℃以上の場合であつて、400
℃より低温となつてから冷却速度を変更してもC
固溶量はほとんど変化しないことがわかる。
調質圧延後の硬さを決定するのは、調質圧延工
程であつて、この調質圧延で最終的な硬さを調整
して所望の調質度の目標硬さを得るのであるが、
調質圧延における硬さ調整には加工硬化が寄与す
るから、その調質圧延における硬さの変化には材
質的には鋼中の固溶元素、特に固溶Cと固溶Nが
大きく関係する。したがつて調質圧延時における
固溶C量の差が大きければ、調質圧延の圧延率に
さほど大きな差がなくとも、大きな硬さ変化を確
実に与えて、異なる調質度に確実に作り分けるこ
とができるのである。ここで、前述のように連続
焼鈍後の冷却過程において徐冷から急冷へ変化さ
せた場合のC固溶量の変化が大きいのは冷却速度
変更温度Tが400℃以上の場合であつて、400℃よ
り低い温度で徐冷から急冷へ変化させても、もは
やC固溶量の変化は極めて少なくなる。このこと
から、調質圧延後の硬さを確実に変化させるべ
く、C固溶量を確実に変化させるためには、連続
焼鈍工程の冷却過程における400℃以上の温度域
での冷却速度を変化させる必要があり、それより
低い温度域での冷却速度は、本質的に影響しない
ことがわかる。一方、第4図から理解されるよう
に、冷却速度変更温度が500℃より高くなつても、
C固溶量の変化量は冷却速度変更温度が500〜400
℃附近の場合とほとんど変わらず、このことか
ら、500〜400℃の温度域の冷却速度制御を確実に
行なうならば、それより高い温度域での冷却速度
制御は不要となることがわかる。結局、500〜400
℃の間のみの冷却速度制御を行なうことによつて
C固溶量を確実に変化させ、調質圧延による硬さ
調整を確実に行なうことができるのである。
このような知見はこの発明にとつて極めて重要
な事項である。すなわち、従来連続焼鈍直後の冷
却速度を変えて調質度を制御するためには、焼鈍
均熱温度から室温付近までの間の冷却速度をその
全域にわたつて制御する必要があるとされてい
た。そのため、従来冷却速度を変えるにあたつて
は、急冷する場合においては低温部における冷却
能率低下が問題となり、一方徐冷する場合におい
ては高温から低温までの冷却に要する時間の増大
による能率の大幅低下が問題となつていたのであ
る。しかるにこの発明では、従来の常識を大きく
覆して、高温から低温までの全域ではなく、500
〜400℃という中間温度域のみの冷却速度制御を
行なうだけで充分であることを見出したのであ
る。
そして上述のような連続焼鈍工程における均熱
保持後の冷却速度が調質圧延後の硬さに及ぼす影
響を詳細に調べた結果、調質度T4の硬さを確実
に得るためには、500〜400℃の間の冷却速度を55
℃/sec以下、好ましくは25℃/sec以下とすれば
良く、一方調質度T5の硬さを確実に得るために
は、同じく500〜400℃の間の冷却速度を65℃/
sec以上、好ましくは70℃/sec以上とすれば良い
ことが判明した。したがつてこれらの条件をこの
発明で規定したのである。
なお連続焼鈍をするに際しては、既に述べたよ
うに冷却速度を制御するに加えて、均熱条件も制
限する必要がある。すなわち焼鈍均熱温度は再結
晶温度以上とする必要があるが高過ぎれば結晶粒
が粗大となるから、上限をA1点とする。また均
熱時間については、長過ぎればAlNの析出が進
行して固溶N量が不足するおそれがあるから、均
熱時間は可及的に短いことが好ましく、通常は5
秒以内とすることが望ましい。
さらにこの発明の方法においては、鋼素材の成
分の制御も極めて重要であり、以下に各成分の限
定理由について説明する。
C:
調質圧延時の固溶C量は、既に述べたように加
工硬化による硬さ上昇の程度に大きな影響を及ぼ
し、またその固溶C量は前述のように連続焼鈍工
程の冷却速度の影響を大きく受ける。そして固溶
C量の変化に対する冷却速度の影響は、鋼中全C
量に大きく依存することが本発明者等の次のよう
な実験により判明しており、したがつてC量の適
切な制御はこの発明で重要である。すなわち種々
のC量の鋼を用い、各C量の鋼についてそれぞれ
第5図のパターンCに示すように500〜400℃の間
の冷却速度を25℃/secとした調質度T4向けの
ヒートサイクルによる熱処理と、第5図のパター
ンDに示すように500〜400℃の間の冷却速度を
100℃/secとした調質度T5向けのヒートサイク
ルによる熱処理とを行ない、パターンCのヒート
サイクルによる固溶C量のパターンDのヒートサ
イクルによる固溶C量の差を調べた。その結果第
6図に示すように、冷却速度の差による固溶C量
の差は、鋼素材中のC量に大きく依存し、C量が
0.02〜0.06%の場合に固溶C量の差が大きく、そ
の範囲を外れる場合には固溶C量の差が著しく小
さくなつてしまうことが判明した。したがつて連
続焼鈍工程での冷却速度を変えることによつて固
溶C量を顕著に変化させて、調質圧延後の硬さの
変化を確実にもたらすためには、素材のC量を
0.02〜0.06%の範囲内とする必要がある。
NおよびAl:
Nは固溶Nとして鋼中に残留することにより、
低圧下の調質圧延で大幅な硬さ変化をもたらすた
めに必要な元素であり、またAlはNと結合して
固溶Nを減少させてしまう有害な作用をもたら
す。したがつてN量、Al量の制御もC量の制御
とならび、この発明において極めて重要である。
この発明では、低圧下の調質圧延によつて最大限
の硬さ変化をもたらすためにはNの固溶量を大き
くしておく必要があり、その効果を充分に発揮さ
せるためには鋼中全N量を、0.004%以上とする
必要がある。一方N量に対してAl量が多くなれ
ば、AlNとしてNが固定されて、固溶N量が少
なくなつてしまう。本発明者等が連続焼鈍後の板
の固溶N量におよぼすN量とAl量との比
(%)/Al(%)の影響について調べたところ、
第7図に示すような結果が得られた。第7図から
明らかなようにN(%)/Al(%)の値が0.15未満
となれば急激に固溶N量が減少する。したがつて
N(%)/Al(%)の値を0.15以上に限定した。ま
たN量があまり多くなれば、相対的に軟質な調質
度T4の原板を得難くなるから、N量の上限を
0.01%とした。なおN量は好ましくは0.008%以
下とすることが望ましい。一方Alは固溶Nを確
保する観点からは少ないことが好ましいが、通常
の製鋼過程においては脱酸のために必要な元素で
あり、そのためには少なくとも0.01%以上の含有
を必要とする。さらにAlが多過ぎれば前述のよ
うに固溶Nを減少させてしまうから、N量との比
N(%)/Al(%)の制限に加えて、Al量の上限
を0.04%とする必要がある。
Mn:
Mnは不可避的不純物として含有されるSによ
る割れを防止するために0.1%以上の添加を必要
とするが、過剰に含有されれば表面性状劣化の原
因となるから、0.1〜0.4%の範囲内とする必要が
ある。
以上のようなC、N、Al、Mnに対する残部は
Feおよび不可避的不純物とすれば良い。
以上のような鋼素材に対する熱間圧延は、常法
に従つて行なえば良いが、その熱間圧延後の熱延
板巻取温度は、この発明の目的を達成するために
は低いことが必要である。特に巻取温度が600℃
を越えれば、NがAlNとして固定され易くなる
のみならず、結晶粒径が大きく大きくなり過ぎて
軟質化するため、調質度T4,T5の作り分けが
困難となる。したがつて熱延板巻取温度は600℃
以下、好ましくは540℃以下とする。
熱延板に対しては必要に応じて酸洗処理を施し
た後、常法に従つて冷間圧延して所望の板厚と
し、次いで連続焼鈍を施す。この連続焼鈍工程に
おける均熱条件は既に述べた通りであり、また均
熱後の冷却過程における500〜400℃の間の平均冷
却速度を最終的に得るべき調質度T4,T5に応
じて変化させることも既に述べた通りである。
連続焼鈍後の調質圧延における圧下率は、調質
度T4を得る場合には1.0〜2.0%とし、一方調質
度T5を得る場合は1.5〜2.5%とする。このよう
に調質圧延圧下率を定めた理由は、この程度の圧
下率であれば通常の調質圧延機の適用が可能であ
り、しかも母材板厚の変更も必要ないからであ
る。ここで、調質度T4を得る場合とT5を得る
場合との間において圧下率に余り差がないが、既
に述べたような化学成分の鋼を素材として前述の
ように連続焼鈍工程の冷却速度に差を持たせるこ
とによつて、この程度の調質圧延圧下率調整によ
り充分に調質度T4,T5の硬さを作り分けるこ
とができるのである。もちろんこの調質圧延にお
いては、小径ワークロールやウエツト調質液など
の特別の手段を講じる必要はない。
以上のようにこの発明の方法においては、化学
成分、熱延条件、焼鈍ヒートサイクル(特に500
〜400℃の間の冷却速度)、調質圧延圧下率を適切
に組合せることによつて、調質度T4の板と調質
度T5の板を同一成分の鋼素材から正確かつ効率
的に作り分けることが可能となつた。ここで、比
較的少ない冷却速度変化、小さい調質圧延圧下率
変化で調質度T4,T5を作り分けることが可能
となつたのは、素材成分の適切な設定によつて固
溶C量、固溶N量を最大限に変化させることに成
功したためと考えられる。
なおこの発明の効果は、ぶりき(スズめつき)
あるいはTFSなどの表面処理の方法によつて変
わるものではなく、したがつてこの発明の方法は
ぶりき用原板、TFS用原板、その他全ての表面
処理用原板の製造に適用することができる。
実施例
第2表の鋼3〜7に示す化学成分の鋼につい
て、それぞれ常法に従つて2.3mm厚まで熱間圧延
して、第3表中に示す巻取温度で巻取り、その熱
延鋼板をさらに0.23mm厚まで冷間圧延し、第5図
のパターンCのヒートサイクルもしくはパターン
Dのヒートサイクルで連続焼鈍した。次いで第3
表中に示す圧下率で調質圧延を施し、続いてスズ
めつきラインにてスズめつきおよびリフロー処理
を施して製品(ブリキ板)とした。各ぶりき板に
ついて硬さ(HR30T)を調べたところ、第3表
中に示す結果が得られた。
第2表、第3表から明らかなように、この発明
の成分範囲内の鋼(鋼番3、5、6)を用いかつ
この発明のプロセス条件範囲内で処理した場合
(実験No.3−1、3−2;5−1、5−2;6−
1、6−2)には、いずれも正確に調質度T4と
T5の硬さに作り分けることができた。これに対
し、この発明の成分範囲内の鋼を用いてもプロセ
ス条件が外れた場合(実験No.3−3、3−4)
や、この発明の成分範囲外の鋼(鋼番4、7)を
用いてこの発明のプロセス条件範囲で実施した場
合(実験No.4−1、4−2;7−1、7−2)に
は、いずれも調質度T4,T5の作り分けが困難
であつた。
発明の効果
前述の説明で明らかなように、この発明の方法
によれば、同一成分の鋼素材を用いて、連続焼鈍
工程の冷却過程のうち500〜400℃の間の冷却速度
を若干変化させかつ調質圧延の圧下率を若干変化
させるだけで、調質度T4の表面処理用原板と調
質度T5の表面処理用原板とを正確に作り分ける
ことができる。
そしてこの発明の方法において調質度T4とT
5を作り分けるために必要なプロセス条件変更
は、前述のように連続焼鈍工程の冷却過程の冷却
速度については500〜400℃の間の冷却速度変更の
みで足りしかもその変更幅も少なくて済むから、
連続焼鈍設備の長大化や処理能率の低下等を招く
おそれがなく、一方調質圧延工程については過大
な高圧下を加えることなく、通常行なわれている
程度の調質圧延圧下率の幅内で変化させれば足り
るから、特殊な調質圧延機を用いたり特殊な操作
を加えたりすることなく、通常の調質圧延機で実
施することができ、しかも高圧下のために製品に
悪影響を及ぼしたり母材板厚の変更を要したりす
ることがない。したがつてこの発明の方法によれ
ば、同一の素材から極めて効率的に調質度T4,
T5の各表面処理用原板を作り分けることができ
る。
Industrial Application Field The present invention is applicable to the production of tin plate or stain-free steel sheet (hereinafter referred to as TFS).
Regarding the manufacturing method of the original plate for surface treatment, in particular, the continuous annealing method is applied to the original plate for surface treatment to the tempering degree of T4 and T5.
This is about how to make them separately. BACKGROUND ART As is well known, tin plate is produced by hot-rolling and cold-rolling a steel material, annealing the cold-rolled steel plate, and then subjecting it to temper rolling if necessary. , usually to obtain the required hardness. The degree of heat treatment of such tin plate is specified as follows by JIS G3303. In other words, the tempering degrees are classified from T1 to T6 in order from the softest, and the target hardness values for each are Rockwell hardness (HR30T), with T1 being 49±3 and T2 being 53±.
3. T3 is 57±3, T4 is 61±3, T5 is 65±
3. T6 is said to be 70±3. Among these tinplate blanks with different degrees of temper, so-called soft plates with degrees of temper T1 to T3 are manufactured by applying the box annealing method to the annealing process, and those with degrees of temper T4 to T6 are manufactured by applying the box annealing method to the annealing process. Hard plates are usually manufactured by applying a continuous annealing method. By the way, how to make different plates for each tempering degree of tin plate obtained by the continuous annealing method with tempering degrees T4 to T6, and in particular, how to make different plates with tempering degree T4 and original plates with tempering degree T5. Conventionally, this was usually done by changing only the chemical composition of the steel material. In other words, the original plate with a heat treatment degree of T4 is made of ordinary bottom carbon steel, while the original plate with a heat treatment degree of T5 is made of copper hardened by adding N and C. In general, inter-rolling conditions, continuous annealing test results, skin pass rolling reduction ratio, etc., were not changed depending on the heat quality degree. The reasons why original plates with heat treatment degrees T4 and T5 were made differently by changing only the chemical composition of the steel material were, first of all, because changing the chemical composition itself was technically easy. The second reason is that it is difficult to change the manufacturing conditions due to the equipment, and the technical basis for doing so has not been established. However, in recent years, the requirements of tin plate base plate users have become even more stringent than before, and they are now required to have hardness that precisely matches the target value. There are cases in which the general methods cannot satisfy the demands of consumers. On the other hand, it is desired to establish a more efficient manufacturing method for the original plate itself, but the production volume of the original plates with the above-mentioned tempering degrees T4 and T5 is large, and Although their uses are similar, in the past they had to be handled separately from the steelmaking stage due to their different chemical compositions, making process control extremely complicated, and improvements are desired. . Therefore, there are several methods that have been proposed in the past to differentiate between T4 and T5 original plates by assuming that the chemical composition of the steel material itself is the same and changing the conditions of the annealing process or adjustment rolling process, which is close to the final process. or has been proposed. For example, JP-A-57-70227 proposes a method of controlling the degree of tempering by changing only the cooling rate during annealing. On the other hand, in JP-A No. 55-114401, a special skin pass rolling mill equipped with work rolls with a diameter of 50 to 300 mm is used to achieve a high rolling reduction of T1 to T6. A method has also been proposed in which plates of all tempering degrees up to 100% are made from the same material. Problems to be Solved by the Invention In order to efficiently produce tinplate blanks with different degrees of tempering, especially blank plates with tempering degrees T4 and T5, the composition of the steel material must be the same, and the final stage of the blank manufacturing process must be the same. It is preferable to control the degree of tempering by controlling the conditions in a process close to the process, and methods for doing so include the method described in JP-A-57-70227, as already mentioned, and the method described in JP-A-55-114401. The method described in the publication is proposed. However, none of these proposed methods is practical, and some new problems may arise. That is, the method described in JP-A-57-70227 is as follows:
By using commonly used bottom carbon Al-killed steel or rimmed steel as a material, and continuously annealing it after hot rolling and cold rolling, the cooling rate after soaking to room temperature is greatly changed. This publication aims to produce plates with a thermal quality of T4 and plates with a thermal quality of T5, and this publication states that in order to obtain a plate with a thermal quality of T4, the cooling rate should be 5 to 20°C/sec, and the temperature should be In order to obtain a plate with quality T5, the cooling rate should be 100 to 300.
It is stated that it is appropriate to set the temperature to ℃/second. Regarding temper rolling after continuous annealing, the rolling reduction rate is the same at 1% for both temper degrees T4 and T5.
is applied. Attempts to change the hardness solely by controlling the cooling rate after annealing have been proposed not only in the above-mentioned publication but also in the past. In order to make different types of annealing, it is necessary to significantly widen the variation range of the cooling rate, which increases the length of continuous annealing equipment and increases operating costs, making it difficult to apply in reality. On the other hand, in the method described in JP-A-55-114401 in which the degree of tempering is controlled by changing the rolling reduction in skin-pass rolling after continuous annealing, according to an example in the same publication, the degree of tempering T4 is In order to make different plates and T5 plates, the temper rolling reduction ratio must be changed significantly. In particular, in order to manufacture a plate with a heat treatment degree of T5, the rolling reduction must be extremely high at 2.7 to 2.8%. In order to obtain such a high rolling reduction, a special work roll with a small diameter is required, as explained in detail in the same publication, and therefore it is impossible to apply a normal skin pass rolling mill. It cannot be manufactured on existing lines. Furthermore, in order to significantly change the skin pass rolling reduction ratio as described above, it is also necessary to change the finished cold rolled plate thickness, resulting in the problem of a significant drop in production efficiency. Furthermore, when the steel is under a high pressure of as much as 2.7 to 2.8%, problems arise such as poor workability and cracking at welds and the like. As mentioned above, in the conventionally proposed methods,
By applying it to reality, we can achieve high production efficiency and heat quality T.
It was not suitable for making different original plates for T4 and T5. This invention was made against the background of the above-mentioned circumstances, and it is possible to surface-treat tin plate or TFS plate with a heat treatment level of T4 from steel materials containing the same chemical composition without incurring the various problems mentioned above. It is an object of the present invention to provide a method for efficiently producing an original plate for surface treatment and an original plate for surface treatment with a heat treatment degree of T5. Means for Solving the Problems As a result of various experiments and studies in order to achieve the above-mentioned purpose, the present inventors used steel with a specific chemical composition as a material, and determined the chemical composition conditions, hot rolling conditions, By appropriately combining the continuous annealing conditions and skin pass rolling reduction ratio, it is possible to efficiently and accurately achieve the heat pass degree T4 without having to change the conditions as much as in the conventionally proposed methods. Surface treatment original plate and heat treatment degree T
They discovered that it is possible to make different types of original plates for surface treatment, as described in No. 5, and came up with this invention. That is, the method of this invention can reduce C 0.02 to 006%.
(weight%, same below), N 0.004-0.01%, Mn
0.1 to 0.4%, Al 0.01 to 0.04%, and the ratio N (%) / Al (%) of N amount to Al amount is 0.15 or more, and the balance is Fe and unavoidable impurities. The hot-rolled sheet is hot-rolled to a coiling temperature of 600℃ or less, then cold-rolled, and then soaked and cooled by continuous annealing to a temperature above the recrystallization temperature and below the Al transformation point, and then tempered. When rolling is performed to produce a surface treatment original plate with a tempering degree of T4 or T5, an average cooling rate between 500 and 400°C in the cooling process after soaking in the continuous annealing,
By setting the rolling reduction rate in skin pass rolling to one of the following conditions (a) and (b) depending on the final temper degree T4 or T5 to be obtained, This method is characterized by separately producing a T4 surface treatment original plate and a T5 surface treatment original plate. (b) For temper degree T4: Average cooling rate 55℃/sec or less, temper rolling reduction rate 1.0 to 2.0% (B) For temper degree T5: Average cooling rate 65℃/sec or higher, temper rolling Rolling reduction rate 1.5-2.5%. Detailed Description of the Invention First, the experimental results that formed the basis of this invention will be explained. As shown in Table 1, low carbon Al killed steels having two different chemical components were hot rolled and cold rolled in a normal process to obtain a cold rolled plate with a thickness of 0.25 mm. Each cold-rolled sheet is subjected to annealing heat treatment using two types of heat cycles shown in Fig. 1, A and B, and then temper-rolled at a rolling rate of about 0.1 to 3.5% in a small rolling mill. was applied. Then, after performing a treatment equivalent to molten tin at 250°C for 3 seconds, the Rockwell hardness (HR30T) was measured. The results are shown in FIG. The experimental results revealed that not only the hardness of each steel differs due to changes in steel composition and heat cycle pattern (change in cooling rate), but also that the dependence of hardness on temper rolling rate changes significantly. That is, for example, in the case of Steel 1, the change in hardness due to a change in heat cycle pattern (change in cooling rate) is relatively small, and the change in hardness due to a change in temper rolling rate is also relatively small. Therefore, in the case of Steel 1, in order to obtain the hardness of temper degree T5, the temper rolling rate should be 3.0.
% or more, and it is found that rolling with a normal temper rolling mill is extremely difficult. On the other hand, Steel 2 has a high sensitivity to heat cycles, and especially when slowly cooled, not only is the hardness small, but the dependence on the skin pass rolling rate is relatively small, and the hardness increases as the skin pass rolling rate increases. While the upward trend is not so great, when the steel is rapidly cooled, the dependence on the skin pass rolling rate becomes significantly large, and the hardness increases rapidly as the skin pass rolling rate increases. Therefore, from these experimental results, if the steel composition is appropriately set, the heat cycle (cooling rate) can be reduced.
The tempering degree T4 and the tempering degree T5 that accurately match the target hardness by appropriately combining the temper rolling rate and the temper rolling rate.
It is expected that it will be possible to efficiently make different plates.
In order to achieve this, it is essential to find a combination of an appropriate component system and an appropriate heat cycle, and it is also essential to find the optimum temper rolling conditions. Therefore, in order to clarify these conditions, more detailed experiments were carried out, and as a result, it was found that the conditions of this invention as already described are necessary, and this invention was completed. Next, each condition in this invention will be explained based on experimental results. First, regarding the cooling rate after soaking and holding at the annealing temperature in the continuous annealing process, the cooling rate is between 500 and 400°C, and when obtaining a tempering degree of T4, the cooling rate is 55°C/sec or less,
In order to obtain a thermal quality of T5, it is necessary to set the temperature to 65°C/sec or higher. In this way, the range for controlling the cooling rate is
The reason why the temperature was defined as between 500 and 400°C was based on the following experimental results. In other words, a cold-rolled plate of Steel 2 in Table 1 with a thickness of 0.25 mm after hot rolling and cold rolling was soaked at 680°C for 5 seconds as shown in Figure 3, and immediately continued to a temperature of 100°C or less. We conducted experiments in which the cooling rate was 25°C/sec, and the cooling rate was 70°C/sec from various temperatures T in the middle of the cooling process at the 25°C/sec cooling rate. The difference in the solid solution amount of C in the steel was investigated when the steel was slowly cooled at 35°C/sec from each temperature T to when it was rapidly cooled at 70°C/sec. The results are shown in FIG. From the results shown in Figure 4, the difference in the amount of C solid solution when changing the cooling rate from slow cooling of 35°C/sec to rapid cooling of 70°C/sec is large because the cooling rate change temperature T is 400°C or higher. and 400
Even if you change the cooling rate after the temperature reaches below ℃,
It can be seen that the amount of solid solution hardly changes. It is the temper rolling process that determines the hardness after temper rolling, and the final hardness is adjusted in this temper rolling to obtain the target hardness of the desired degree of temper rolling.
Since work hardening contributes to hardness adjustment during temper rolling, the change in hardness during temper rolling is largely related to solid solute elements in the steel, particularly solute C and solid solute N. . Therefore, if there is a large difference in the amount of solid solute C during skin pass rolling, even if there is not a very large difference in the rolling ratio during skin pass rolling, a large change in hardness can be reliably imparted and different degrees of heat rolling can be reliably produced. It can be divided. Here, as mentioned above, when changing from slow cooling to rapid cooling in the cooling process after continuous annealing, the change in the amount of C solid solution is large when the cooling rate change temperature T is 400°C or higher. Even if the cooling is changed from slow cooling to rapid cooling at a temperature lower than ℃, the change in the amount of C solid solution becomes extremely small. Therefore, in order to reliably change the hardness after skin pass rolling and to reliably change the amount of C solid solution, it is necessary to change the cooling rate in the temperature range of 400°C or higher in the cooling process of the continuous annealing process. It can be seen that the cooling rate in a lower temperature range has essentially no effect. On the other hand, as understood from Figure 4, even if the cooling rate change temperature is higher than 500℃,
The amount of change in the amount of C solid solution is determined by the cooling rate change temperature of 500 to 400.
This is almost the same as in the case around 500°C, and this shows that if cooling rate control in the temperature range of 500 to 400°C is performed reliably, cooling rate control in higher temperature ranges becomes unnecessary. In the end, 500-400
By controlling the cooling rate only between 0.degree. Such knowledge is extremely important for this invention. In other words, conventionally, in order to control the degree of tempering by changing the cooling rate immediately after continuous annealing, it was necessary to control the cooling rate over the entire range from the annealing soaking temperature to around room temperature. . Therefore, when changing the cooling rate conventionally, there is a problem of a decrease in cooling efficiency in the low-temperature part when cooling rapidly, while when cooling slowly, the efficiency significantly increases due to the increase in the time required to cool from high temperature to low temperature. The decline was becoming a problem. However, this invention greatly overturns the conventional wisdom, and instead of covering the entire range from high to low temperatures,
They found that it is sufficient to control the cooling rate only in the intermediate temperature range of ~400°C. As a result of a detailed study of the influence of the cooling rate after soaking in the continuous annealing process described above on the hardness after temper rolling, it was found that in order to reliably obtain the hardness of temper degree T4, 55 cooling rate between ~400℃
℃/sec or less, preferably 25℃/sec or less. On the other hand, in order to reliably obtain the hardness of heat treatment degree T5, the cooling rate between 500 and 400℃ should be 65℃/sec or less.
It has been found that the temperature can be set to sec or more, preferably 70°C/sec or more. Therefore, these conditions are defined in this invention. Note that when performing continuous annealing, in addition to controlling the cooling rate as described above, it is also necessary to limit the soaking conditions. That is, the annealing soaking temperature needs to be equal to or higher than the recrystallization temperature, but if it is too high, the crystal grains will become coarse, so the upper limit is set at point A1 . Regarding the soaking time, if the soaking time is too long, the precipitation of AlN may progress and the amount of solid solution N may be insufficient, so it is preferable that the soaking time is as short as possible.
It is desirable to do this within seconds. Furthermore, in the method of the present invention, it is extremely important to control the components of the steel material, and the reasons for limiting each component will be explained below. C: As mentioned above, the amount of solid solute C during skin pass rolling has a large effect on the degree of increase in hardness due to work hardening, and as mentioned above, the amount of solid solute C has a large effect on the cooling rate of the continuous annealing process. greatly affected. The effect of the cooling rate on the change in the amount of solid solute C is that the total C in the steel is
It has been found through the following experiments by the inventors that the carbon content greatly depends on the carbon content, and therefore, appropriate control of the carbon content is important in this invention. In other words, steels with various C contents were used, and heat for temper degree T4 was set at a cooling rate of 25 °C/sec between 500 and 400 °C as shown in pattern C in Fig. 5 for each steel with a different C content. Cyclic heat treatment and cooling rate between 500 and 400℃ as shown in pattern D in Figure 5.
A heat treatment was performed using a heat cycle for a thermal quality T5 at 100°C/sec, and the difference in the amount of solid solute C due to the heat cycle of pattern C and the amount of solid solute C due to the heat cycle of pattern D was investigated. As a result, as shown in Figure 6, the difference in the amount of solid solute C due to the difference in cooling rate largely depends on the amount of C in the steel material, and
It has been found that the difference in the amount of solid solute C is large when the amount is 0.02 to 0.06%, and the difference in the amount of solute C becomes significantly small when the amount is outside of this range. Therefore, in order to noticeably change the amount of solid solute C by changing the cooling rate in the continuous annealing process and reliably bring about a change in hardness after temper rolling, it is necessary to increase the amount of C in the material.
It must be within the range of 0.02 to 0.06%. N and Al: N remains in the steel as solid solution N,
Al is an element necessary to bring about a large change in hardness during temper rolling under low pressure, and Al also has the harmful effect of reducing solid solution N by combining with N. Therefore, controlling the amount of N and the amount of Al as well as controlling the amount of C is extremely important in this invention.
In this invention, in order to bring about the maximum change in hardness through low-reduction temper rolling, it is necessary to increase the amount of solid solution of N, and in order to fully demonstrate its effect, it is necessary to increase the amount of solid solution in the steel. The total amount of N needs to be 0.004% or more. On the other hand, if the amount of Al increases relative to the amount of N, N will be fixed as AlN and the amount of solid solution N will decrease. When the present inventors investigated the influence of the ratio (%) of the amount of N to the amount of Al/Al (%) on the amount of solid solution N in the plate after continuous annealing, it was found that
The results shown in FIG. 7 were obtained. As is clear from FIG. 7, when the value of N (%)/Al (%) becomes less than 0.15, the amount of solid solution N decreases rapidly. Therefore, the value of N (%)/Al (%) was limited to 0.15 or more. Also, if the amount of N is too large, it will be difficult to obtain a relatively soft base plate with a heat treatment degree of T4, so the upper limit of the amount of N should be set.
It was set as 0.01%. Note that the amount of N is preferably 0.008% or less. On the other hand, Al is preferably contained in a small amount from the viewpoint of ensuring solid solution N, but it is an element necessary for deoxidation in the normal steelmaking process, and for this purpose, it needs to be contained at least 0.01% or more. Furthermore, if there is too much Al, the solid solution N will be reduced as mentioned above, so in addition to limiting the ratio N (%)/Al (%), it is necessary to set the upper limit of the Al amount to 0.04%. There is. Mn: Mn needs to be added in an amount of 0.1% or more to prevent cracking due to S, which is included as an unavoidable impurity. Must be within the range. The remainder for C, N, Al, and Mn as above is
Fe and unavoidable impurities may be used. Hot rolling of the above-mentioned steel materials may be carried out according to a conventional method, but the winding temperature of the hot rolled sheet after hot rolling must be low in order to achieve the purpose of the present invention. It is. Especially when the winding temperature is 600℃
If it exceeds this, not only will N be more likely to be fixed as AlN, but the crystal grain size will become too large and soft, making it difficult to differentiate between the degrees of tempering T4 and T5. Therefore, the hot-rolled sheet winding temperature is 600℃.
Hereinafter, the temperature is preferably 540°C or less. The hot-rolled sheet is pickled if necessary, then cold-rolled to a desired thickness according to a conventional method, and then continuously annealed. The soaking conditions in this continuous annealing process are as described above, and the average cooling rate between 500 and 400°C in the cooling process after soaking changes depending on the final degrees of heat treatment T4 and T5. As already mentioned, it is also possible to The reduction ratio in temper rolling after continuous annealing is 1.0 to 2.0% when obtaining a temper degree T4, and 1.5 to 2.5% when obtaining a temper degree T5. The reason why the skin pass rolling reduction ratio is determined in this manner is that a normal skin pass rolling mill can be applied with this level of reduction ratio, and there is no need to change the base material plate thickness. Here, there is not much difference in the reduction rate between obtaining the tempering degree T4 and T5, but the cooling rate in the continuous annealing process as described above is By creating a difference in the tempering degrees, it is possible to sufficiently create different hardnesses of tempering degrees T4 and T5 by adjusting the rolling reduction ratio in temper rolling to this extent. Of course, in this temper rolling, there is no need to take special measures such as small-diameter work rolls or wet tempering fluid. As described above, in the method of this invention, the chemical composition, hot rolling conditions, annealing heat cycle (especially 500
By appropriately combining the cooling rate (cooling rate between It became possible to make them separately. Here, it is possible to create different degrees of heat treatment T4 and T5 with a relatively small change in cooling rate and a small change in reduction rate in skin pass rolling, by appropriately setting the material components, the amount of solid solute C, This is thought to be due to the fact that we succeeded in changing the amount of solid solution N to the maximum extent possible. Furthermore, the effect of this invention is that tinplate (tinplate)
Moreover, it does not change depending on the surface treatment method such as TFS, and therefore, the method of the present invention can be applied to the production of tin plates, TFS plates, and all other surface treatment plates. Examples Steels with chemical compositions shown in Steels 3 to 7 in Table 2 were hot rolled to a thickness of 2.3 mm according to the conventional method, and coiled at the coiling temperature shown in Table 3. The steel plate was further cold rolled to a thickness of 0.23 mm and continuously annealed using a heat cycle of pattern C or a heat cycle of pattern D in FIG. Then the third
Temper rolling was performed at the rolling reduction ratio shown in the table, followed by tin plating and reflow treatment on a tin plating line to produce a product (tin plate). When the hardness (HR30T) of each tin plate was examined, the results shown in Table 3 were obtained. As is clear from Tables 2 and 3, when steels (steel numbers 3, 5, and 6) within the composition range of this invention were used and processed within the process condition range of this invention (Experiment No. 3- 1, 3-2; 5-1, 5-2; 6-
1 and 6-2), it was possible to accurately produce hardnesses of T4 and T5. On the other hand, when the process conditions are out of range even if steel within the composition range of this invention is used (Experiment No. 3-3, 3-4)
Or, when conducted under the process condition range of this invention using steels (steel numbers 4 and 7) outside the composition range of this invention (Experiment No. 4-1, 4-2; 7-1, 7-2) In both cases, it was difficult to differentiate between the tempering degrees T4 and T5. Effects of the Invention As is clear from the above explanation, according to the method of the present invention, the cooling rate between 500 and 400°C in the cooling process of the continuous annealing process is slightly changed using steel materials with the same composition. In addition, by only slightly changing the rolling reduction ratio of skin pass rolling, it is possible to accurately produce a surface treatment base plate having a heat quality degree of T4 and a surface treatment base plate having a heat quality degree of T5. In the method of this invention, the tempering degrees T4 and T
As mentioned above, the only change in process conditions necessary to create different types of 5 is to change the cooling rate between 500 and 400℃ in the cooling process of the continuous annealing process, and the range of change is small. ,
There is no risk of increasing the length of continuous annealing equipment or reducing processing efficiency, and on the other hand, the skin pass rolling process can be carried out within the normal skin pass rolling reduction range without applying an excessively high reduction. Since it is sufficient to change the temperature, it can be carried out in a normal temper rolling mill without using a special temper rolling mill or adding special operations, and the high rolling pressure does not adversely affect the product. There is no need to change the thickness of the base material. Therefore, according to the method of the present invention, the same material can be extremely efficiently heated to a temperature of T4,
Each type of T5 surface treatment original plate can be made separately.
【表】【table】
【表】【table】
第1図はこの発明をなすに至る基礎となつた実
験における焼鈍ヒートサイクルのパターンを示す
線図、第2図は硬さに及ぼす焼鈍ヒートサイクル
パターンと調質圧延圧下率の影響を示す図、第3
図は第4図の実験におけるヒートサイクルのパタ
ーンを示す図、第4図は焼鈍後の冷却過程におい
て徐冷から急冷へ変化させる冷却速度変更温度が
固溶C量変化に及ぼす影響を示すグラフ、第5図
はこの発明の方法における連続焼鈍工程のヒート
サイクルパターンの一例を示す線図、第6図は固
溶C量に及ぼす鋼素材中のC量の影響を示すグラ
フ、第7図は鋼中のN(%)/Al(%)の値が固
溶N量に及ぼす影響を示すグラフである。
Fig. 1 is a diagram showing the annealing heat cycle pattern in the experiment that was the basis for making this invention, Fig. 2 is a diagram showing the influence of the annealing heat cycle pattern and temper rolling reduction rate on hardness, Third
The figure is a diagram showing the heat cycle pattern in the experiment shown in Figure 4, and Figure 4 is a graph showing the influence of the cooling rate change temperature, which is changed from gradual cooling to rapid cooling, on the change in the amount of solid solute C in the cooling process after annealing. Fig. 5 is a diagram showing an example of the heat cycle pattern of the continuous annealing process in the method of the present invention, Fig. 6 is a graph showing the influence of the amount of C in the steel material on the amount of solid solution C, and Fig. 7 is the graph showing the effect of the amount of C in the steel material on the amount of solid solution C. It is a graph showing the influence of the value of N (%)/Al (%) in the solid solution N amount.
Claims (1)
〜0.01%、Mn0.1〜0.4%、Al0.01〜0.04%を含有
し、かつN量とAl量との比N(%)/Al(%)が
0.15以上とされ、残部がFeおよび不可避的不純物
よりなる鋼を素材とし、熱延板巻取温度600℃以
下となるように熱間圧延した後冷間圧延し、さら
に連続焼鈍により再結晶温度以上、A1変態点以
下の温度に均熱して冷却し、その後調質圧延を行
なつて、調質度T4もしくはT5の表面処理用原
板を製造するにあたり、 前記連続焼鈍における均熱後の冷却過程におけ
る500〜400℃の間の平均冷却速度と、調質圧延に
おける圧下率とを、最終的に得るべき調質度T4
もしくはT5に応じて次の(イ)、(ロ)のうちのいずれ
かの条件に設定して、調質度T4の表面処理用原
板と調質度T5の表面処理用原板を作り分けるこ
とを特徴とする連続焼鈍による表面処理用原板の
製造方法。 (イ) 調質度T4の場合: 平均冷却速度55℃/sec以下、調質圧延圧下
率1.0〜2.0%。 (ロ) 調質度T5の場合: 平均冷却速度65℃/sec以上、調質圧延圧下
率1.5〜2.5%。[Claims] 1 C0.02 to 0.06% (weight%, same hereinafter), N0.004
~0.01%, Mn0.1~0.4%, Al0.01~0.04%, and the ratio of N amount to Al amount N (%) / Al (%)
0.15 or higher, with the balance consisting of Fe and unavoidable impurities, the material is hot rolled to a hot rolled sheet coiling temperature of 600℃ or lower, then cold rolled, and then continuously annealed to a temperature higher than the recrystallization temperature. , in the cooling process after soaking in the continuous annealing, when soaking and cooling to a temperature below the A1 transformation point, and then performing temper rolling to produce a surface treatment base plate with a temper degree of T4 or T5. The average cooling rate between 500 and 400°C and the rolling reduction in temper rolling are the final temper degree T4.
Alternatively, set either of the following conditions (a) or (b) depending on T5 to separately produce a surface treatment original plate with a thermal quality of T4 and a surface treatment original plate with a thermal quality of T5. A method for manufacturing original plates for surface treatment using continuous annealing. (a) In the case of temper degree T4: average cooling rate of 55°C/sec or less, temper rolling reduction rate of 1.0 to 2.0%. (b) In the case of temper degree T5: average cooling rate of 65°C/sec or more, temper rolling reduction rate of 1.5 to 2.5%.
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP11458185A JPS61272323A (en) | 1985-05-28 | 1985-05-28 | Manufacture of original sheet for surface treatment by continuous annealing |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP11458185A JPS61272323A (en) | 1985-05-28 | 1985-05-28 | Manufacture of original sheet for surface treatment by continuous annealing |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| JPS61272323A JPS61272323A (en) | 1986-12-02 |
| JPH0545653B2 true JPH0545653B2 (en) | 1993-07-09 |
Family
ID=14641425
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP11458185A Granted JPS61272323A (en) | 1985-05-28 | 1985-05-28 | Manufacture of original sheet for surface treatment by continuous annealing |
Country Status (1)
| Country | Link |
|---|---|
| JP (1) | JPS61272323A (en) |
Families Citing this family (6)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| CN1145709C (en) * | 2000-02-29 | 2004-04-14 | 川崎制铁株式会社 | High-strength cold-rolled steel sheet excellent in strain-age hardening properties and method for producing the same |
| US20030015263A1 (en) | 2000-05-26 | 2003-01-23 | Chikara Kami | Cold rolled steel sheet and galvanized steel sheet having strain aging hardening property and method for producing the same |
| CN1158398C (en) * | 2000-05-26 | 2004-07-21 | 杰富意钢铁株式会社 | Cold rolled steel sheet having strain age hardening property, galvanized steel sheet and manufacturing method thereof |
| EP1291447B1 (en) * | 2000-05-31 | 2005-05-04 | JFE Steel Corporation | Cold-rolled steel sheet having excellent strain aging hardening properties and method for producing the same |
| KR100946132B1 (en) * | 2002-09-30 | 2010-03-10 | 주식회사 포스코 | Manufacturing method of tin plated disc |
| JP5668361B2 (en) * | 2009-08-21 | 2015-02-12 | Jfeスチール株式会社 | High tensile cold-rolled steel sheet and method for producing the same |
Family Cites Families (4)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JPS5548574B2 (en) * | 1974-03-12 | 1980-12-06 | ||
| JPS50139013A (en) * | 1974-04-27 | 1975-11-06 | ||
| JPS5141623A (en) * | 1974-10-05 | 1976-04-08 | Nippon Steel Corp | Renzokushodonnyoru nanshitsunahyomenshoryokohanno seizoho |
| JPS5857490A (en) * | 1981-10-02 | 1983-04-05 | Toa Gurauto Kogyo Kk | Muddy water composition for stabilizing excavated surface |
-
1985
- 1985-05-28 JP JP11458185A patent/JPS61272323A/en active Granted
Also Published As
| Publication number | Publication date |
|---|---|
| JPS61272323A (en) | 1986-12-02 |
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