JPH0448865B2 - - Google Patents

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Publication number
JPH0448865B2
JPH0448865B2 JP15255585A JP15255585A JPH0448865B2 JP H0448865 B2 JPH0448865 B2 JP H0448865B2 JP 15255585 A JP15255585 A JP 15255585A JP 15255585 A JP15255585 A JP 15255585A JP H0448865 B2 JPH0448865 B2 JP H0448865B2
Authority
JP
Japan
Prior art keywords
less
sol
hot rolling
defects
steel
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
Application number
JP15255585A
Other languages
Japanese (ja)
Other versions
JPS6213556A (en
Inventor
Setsuo Kakihara
Makoto Kobayashi
Hiroyuki Kakiuchi
Akya Yagishima
Keiichi Yoshioka
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
JFE Steel Corp
Original Assignee
Kawasaki Steel Corp
Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)
Filing date
Publication date
Application filed by Kawasaki Steel Corp filed Critical Kawasaki Steel Corp
Priority to JP15255585A priority Critical patent/JPS6213556A/en
Publication of JPS6213556A publication Critical patent/JPS6213556A/en
Publication of JPH0448865B2 publication Critical patent/JPH0448865B2/ja
Granted legal-status Critical Current

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Classifications

    • CCHEMISTRY; METALLURGY
    • C21METALLURGY OF IRON
    • C21DMODIFYING THE PHYSICAL STRUCTURE OF FERROUS METALS; GENERAL DEVICES FOR HEAT TREATMENT OF FERROUS OR NON-FERROUS METALS OR ALLOYS; MAKING METAL MALLEABLE, e.g. BY DECARBURISATION OR TEMPERING
    • C21D9/00Heat treatment, e.g. annealing, hardening, quenching or tempering, adapted for particular articles; Furnaces therefor
    • C21D9/0081Heat treatment, e.g. annealing, hardening, quenching or tempering, adapted for particular articles; Furnaces therefor for slabs; for billets

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  • Chemical & Material Sciences (AREA)
  • Engineering & Computer Science (AREA)
  • Physics & Mathematics (AREA)
  • Thermal Sciences (AREA)
  • Crystallography & Structural Chemistry (AREA)
  • Mechanical Engineering (AREA)
  • Materials Engineering (AREA)
  • Metallurgy (AREA)
  • Organic Chemistry (AREA)
  • Heat Treatment Of Steel (AREA)

Description

【発明の詳細な説明】[Detailed description of the invention]

(産業上の利用分野) 本発明は、ステンレス合金鋼、特に、熱間圧延
時に割れによる表面疵の発生が少ないステンレス
合金鋼およびそのスラブ加熱方法に関するもので
ある。 (従来の技術) ステンレス合金鋼を熱間圧延する際に問題とな
る主な表面欠陥の一つに通常線ヘゲ(スリバー)
と呼ばれている線状のヘゲ疵がある。この欠陥は
冷間圧延しても消失せず、また、多くの場合、熱
延コイルでは発見できない微細なヘゲ疵が冷間圧
延で顕著化するため大きな問題となつている。表
面品質が重要視されるステンレス合金鋼では、上
述の欠陥は致命的であり、歩留まり低下のため、
大幅なコストアツプを招いている。 上述の欠陥発生の理論的解明は必ずしも十分で
はないが、一般的には、鋳造擬固時の旧オーステ
ナイト粒界の脆化に起因していると考えられてい
る。これは、旧オーステナイト粒界には硫黄や酸
素が濃化しており、加熱中に硫化物、酸化物が生
成し、これが熱間圧延時に脆化を促進し、小さな
割れが生じ、ヘゲ疵となつていると推定されてい
る。そのため、これを防止するには、鋼中の硫黄
や酸素含有量を低減するか、無害化する必要があ
つた。 上述したように、熱間圧延時の割れによる表面
疵の発生を防止するには、鋼中の硫黄および酸素
の含有量を極力低減することが効果的であるが、
現実的にはコスト高となり、低減にも限度があ
る。 従来、熱延時の割れを防止する方法として特開
昭57−16153号公報に記載されているように、
δCal(δフエライト量の計算値)=3(Cr+Mo+
1.5Si+0.5Nb)−2.8(Ni+1/2Mn+1/2Cu)−84
(C+N)−19.8で決まるδCalを4.0%以下にする
方法、特開昭57−127506号公報に記載されている
ように、連鋳時の溶鋼加熱度ΔT(液相線温度と
鋳造温度の差)とN値の積に応じて加熱炉のスラ
ブ加熱温度を調整する方法、Ti等の特殊成分を
添加して熱間強度の向上を図る方法等が知られて
いる。 第1の方法は、熱延時の脆化原因であるδフエ
ライトの計算値δCalを4.0%以下に押さえようと
するものである。しかし、実際にはステンレス合
金鋼の成分は機械的特性、耐食性等を考慮して設
定されるもので、δCal値をO近傍に合わせるこ
とを、多くの鋼種について満足させることは難し
い。さらにステンレス合金鋼溶製時において目標
設定成分に100%適中させることは難しく、実用
上問題がある。また、第2の方法はチヤージ毎あ
るいは連続鋳造中、ΔT及びN量は変化し、雑多
の覆歴を持つスラブを同時に多数加熱する必要の
ある加熱炉の操業で、全スラブを対象に制御する
ことは実際上不可能である。 さらに、第3の特殊成分の添加、例えばTi添
加は、介在物増加によりストリンガー疵等の疵が
増加するし、高価な特殊合金成分添加によるコス
トアツプが著しい。 (発明が解決しようとする問題点) 本発明は、上述した熱間圧延時に、鋼中の硫黄
や酸素を無害化して割れによる表面疵の発生を防
止し得るステンレス合金鋼を提供しようとするも
のである。 (問題点を解決するための手段) 本発明は、C:0.001〜0.20wt%(以下単に%
で表す)、Si:0.10〜5.0%、Mn:0.1〜11.0%、
P:0.050%以下、S:0.020%以下、Cr:11.0〜
30.0%、Ni:2.0〜30%、N:0.001〜0.160%、
O:0.015%以下を含有し、さらに耐食性向上元
素としてMo:5.0%以下、Cu:3.0%以下、Nb:
1.0%以下およびSn:0.10%以下の1種または2
種以上を含み、さらに熱延時の表面割れ防止元素
として、Ti:0.05%以下、Zr:0.10%以下、Ca:
0.006%以下およびB:0.05%以下の1種または
2種以上を含み、sol Alを0.001〜0.005%含有し、
残部がFeおよび不可避不純物よりなる熱間圧延
で表面割れの少ないステンレス合金鋼を特徴とす
る。 (作用) 本発明によれば、優れた耐食性を有し、しかも
熱間圧延時に発生する割れによる表面欠陥を大幅
に減少させることができる。 次に、各成分の限定理由を述べる。 Cは、耐食性の点からは、低いほど良く、また
耐熱性の点からは高い方が良いが、実用を考慮し
0.001〜0.20%とした。 Siは、加工性の点からは低い方が良いが、低す
ぎると、脱酸が不十分となる。そこで、下限を
0.1%とし、5%を超えると脆化が著しくなるた
め上限を5.0%とした。 Mnは、低すぎると加工性が劣化し、また、脱
酸も不十分になるので、下限を0.1%とした。ま
た、多いほどオーステナイトが安定し、加工性、
耐食性にも良いが、効果が飽和するので11.0%を
上限とした。 Pは、高くなると、加工性・耐食性が悪くなる
ので、上限を0.050%とした。 Sは、熱間加工性を劣化させる。特に、凝固時
オーステナイト粒界に偏析し、熱間圧延時に発生
する線状ヘゲ疵の主因になる。したがつて上限は
0.020%とすべきである。 Oも、Sと同じ理由で低い方が良く、上限を
0.015%にした。 Crは、ステンレス鋼としての耐食性から11.0%
が下限であり、脆性と加工が困難になることを考
慮して上限を30%にした。 Niは、Cr量との関連があるが、この関連と、
オーステナイト相の安定性とを考慮して2.0%以
上とした。上限はコスト上の問題から30%に押さ
えた。 Nは、オーステナイト相を安定させる意味では
多い方が良いが、固溶量の限界を考慮して上限を
0.160%とし、下限は製造上の限界をもつて0.001
%とした。 Moは、耐食性向上元素として、用途により5.0
%以下で選択添加できる。 Cuは、耐食性向上元素として有効であるが、
加工性と、圧延時の割れの問題から3.0%を上限
として選択添加できる。 Nbは、耐食性向上元素として有効であるが、
脆化の問題から上限を1.0%として選択添加でき
る。 Snは、耐食性向上元素として、効果が飽和す
る0.10%以下で選択添加できる。 Tiは、熱延時の表面割れ防止元素として選択
添加され、安定の硫化物を形成すると同時に微細
化によつて、熱延時の表面割れを防止する作用が
あるが、しかし多量に添加するとチタンストリン
ガー疵の原因にもなるため、用途により少量選択
添加すべきで、効果の飽和点0.05%をもつて上限
とする。 Zrは、熱延時の表面割れ防止元素として、Ti
と同様の効果があるが、コストと効果の飽和を考
慮して0.10%を上限として選択添加する。 Caは、熱延時の表面割れ防止元素として介在
物形態制御に効果があるが、耐食性を劣化させる
作用を有するため、0.006%を上限として、用途
により選択添加する。 Bは、熱延時の表面割れ防止元素として選択添
加されるが、0.05%を超えると耐粒界腐食性を著
しく低下させるので0.05%以下で選択添加する。 sol Alは、以下に述べるように、0.001〜0.05%
含有させることにより熱延時の表面割れを防止す
る上に顕著な効果を有するので、下限を0.001%
とし、上限を0.005%とした。 第1図は、SUS304を例にとつて、sol Alと熱
間圧延後の熱延コイルの表面欠陥(ヘゲ疵および
介在物起因の表面疵)発生率%(疵発生枚数/全
圧延枚数)との関係を示す。 第1図から明らかなように、Alをsol Alとし
て0.001〜0.005%含有させることにより、加熱中
にスラブ表面から侵入する酸素と、元々鋼中に存
在する酸素を結晶粒内に微細なAl2O3として分散
させることで無害化して固定する。sol Al量が
0.005%より多くなると、鋳造時に、溶鋼中のAl
が、溶鋼中の酸素または外来酸素と、Al2O3とし
て結合し、連続鋳造用タンデイツシユノズルで析
出する。その結果、ノズルを閉塞し、鋳造が非常
に困難になる。従来AlはSiと共に溶製時の脱酸
剤として用いられているが、Alは連続鋳造時の
ノズル詰まりの原因となるのでsol Alとして残留
しないように小量添加されている。本発明では、
ノズル詰まりを生じさせない程度の小量のsol Al
を残留させることにより、表面疵が減少すること
を知見したものである。 sol Al添加の効果をSUS304を例にとつてグリ
ーブルテストした結果を第2図に示す。なお、供
試材の成分は第1表の通りである。各試片を1300
℃に20秒で加熱し、この温度に50秒保持した後、
水冷し、−100℃/分の冷却速度で冷却した後、グ
リーブルテストした。このテストからも明らかな
ように本発明鋼の高温における変形能は非常に良
好であることがわかる。これは、高温加熱時の内
部酸化、特に、旧γ粒界での酸化が抑制されてい
るためであると推定される。
(Industrial Application Field) The present invention relates to a stainless alloy steel, particularly a stainless alloy steel that generates fewer surface defects due to cracks during hot rolling, and a method for heating a slab thereof. (Conventional technology) One of the main surface defects that occur when hot rolling stainless steel alloys is normal line sliver (sliver).
There are linear scratches called. These defects do not disappear even after cold rolling, and in many cases, minute sagging defects that cannot be detected in hot-rolled coils become noticeable during cold rolling, posing a major problem. For stainless steel alloys, where surface quality is important, the above defects are fatal and reduce yields.
This has led to a significant increase in costs. Although the theoretical elucidation of the above-described defect occurrence is not necessarily sufficient, it is generally believed that it is caused by the embrittlement of prior austenite grain boundaries during pseudo-solidification during casting. This is because sulfur and oxygen are concentrated in the prior austenite grain boundaries, and sulfides and oxides are generated during heating, which promotes embrittlement during hot rolling, causing small cracks and sagging defects. It is estimated that it has become popular. Therefore, in order to prevent this, it was necessary to reduce the sulfur and oxygen contents in the steel, or to make it harmless. As mentioned above, in order to prevent the occurrence of surface flaws due to cracks during hot rolling, it is effective to reduce the content of sulfur and oxygen in steel as much as possible.
In reality, the cost is high and there are limits to how much it can be reduced. Conventionally, as a method for preventing cracking during hot rolling, as described in Japanese Patent Application Laid-open No. 57-16153,
δCal (calculated value of δ ferrite amount) = 3 (Cr + Mo +
1.5Si+0.5Nb)-2.8(Ni+1/2Mn+1/2Cu)-84
As described in Japanese Patent Application Laid-open No. 57-127506, the method of reducing δCal determined by (C+N)-19.8 to 4.0% or less, the heating degree ΔT of molten steel during continuous casting (difference between liquidus temperature and casting temperature) ) and the N value, a method of adjusting the slab heating temperature in a heating furnace, and a method of adding a special component such as Ti to improve hot strength are known. The first method is to suppress the calculated value δCal of δ ferrite, which is the cause of embrittlement during hot rolling, to 4.0% or less. However, in reality, the components of stainless alloy steel are determined taking into consideration mechanical properties, corrosion resistance, etc., and it is difficult to satisfy the δCal value near O for many steel types. Furthermore, it is difficult to achieve 100% target composition during melting of stainless alloy steel, which poses a practical problem. The second method is a heating furnace operation in which ΔT and N amount change during each charge or during continuous casting, and it is necessary to simultaneously heat a large number of slabs with miscellaneous covering histories, so all slabs are controlled. This is practically impossible. Furthermore, addition of a third special component, for example, addition of Ti, increases the number of defects such as stringer defects due to the increase in inclusions, and the addition of expensive special alloy components significantly increases costs. (Problems to be Solved by the Invention) The present invention aims to provide a stainless steel alloy that can render the sulfur and oxygen in the steel harmless and prevent the occurrence of surface flaws due to cracks during hot rolling as described above. It is. (Means for solving the problems) The present invention provides C: 0.001 to 0.20wt% (hereinafter simply %
), Si: 0.10-5.0%, Mn: 0.1-11.0%,
P: 0.050% or less, S: 0.020% or less, Cr: 11.0~
30.0%, Ni: 2.0~30%, N: 0.001~0.160%,
Contains O: 0.015% or less, and further contains Mo: 5.0% or less, Cu: 3.0% or less, Nb:
1.0% or less and Sn: 0.10% or less Type 1 or 2
In addition, as elements for preventing surface cracking during hot rolling, Ti: 0.05% or less, Zr: 0.10% or less, Ca:
Contains one or more of 0.006% or less and B: 0.05% or less, and contains 0.001 to 0.005% sol Al,
It is characterized by a hot-rolled stainless steel alloy with minimal surface cracks, the remainder of which is Fe and unavoidable impurities. (Function) According to the present invention, it has excellent corrosion resistance and can significantly reduce surface defects due to cracks that occur during hot rolling. Next, the reasons for limiting each component will be described. From the point of view of corrosion resistance, the lower the value of C, the better, and from the point of view of heat resistance, the higher the value, the better.
It was set at 0.001 to 0.20%. From the viewpoint of processability, it is better to have a low Si content, but if it is too low, deoxidation will be insufficient. Therefore, the lower limit
The upper limit was set at 0.1%, and since embrittlement becomes significant when it exceeds 5%, the upper limit was set at 5.0%. If Mn is too low, processability deteriorates and deoxidation becomes insufficient, so the lower limit was set at 0.1%. In addition, the more the austenite is, the more stable the austenite becomes, and the processability becomes better.
Although it is good for corrosion resistance, the effect reaches saturation, so the upper limit was set at 11.0%. As P increases, workability and corrosion resistance deteriorate, so the upper limit was set at 0.050%. S deteriorates hot workability. In particular, it segregates at austenite grain boundaries during solidification and becomes the main cause of linear heave defects that occur during hot rolling. Therefore the upper limit is
Should be 0.020%. For the same reason as S, it is better for O to be lower, and the upper limit is
It was set to 0.015%. Cr is 11.0% due to its corrosion resistance as stainless steel.
is the lower limit, and the upper limit was set at 30% in consideration of brittleness and processing difficulties. Ni has a relationship with the amount of Cr, but this relationship and
Considering the stability of the austenite phase, the content was set at 2.0% or more. The upper limit was set at 30% due to cost considerations. Although it is better to have a large amount of N in order to stabilize the austenite phase, the upper limit should be set in consideration of the limit of solid solution amount.
0.160%, and the lower limit is 0.001 due to manufacturing limitations.
%. Mo is an element that improves corrosion resistance, depending on the application.
It can be selectively added in amounts below %. Cu is effective as an element for improving corrosion resistance, but
From the viewpoint of workability and cracking during rolling, it can be added selectively with an upper limit of 3.0%. Nb is effective as an element for improving corrosion resistance, but
Due to the problem of embrittlement, it can be added selectively with an upper limit of 1.0%. Sn can be selectively added as a corrosion resistance improving element at 0.10% or less at which the effect is saturated. Ti is selectively added as an element to prevent surface cracking during hot rolling, and has the effect of preventing surface cracking during hot rolling by forming stable sulfides and at the same time making it finer.However, if added in large amounts, titanium stringer flaws may occur. Since it can also be a cause of oxidation, it should be added in small amounts selectively depending on the application, and the upper limit is set at the saturation point of 0.05%. Zr is used as an element to prevent surface cracking during hot rolling.
It has a similar effect, but considering cost and effect saturation, it is added at an upper limit of 0.10%. Ca is effective in controlling the form of inclusions as an element to prevent surface cracking during hot rolling, but since it has the effect of deteriorating corrosion resistance, it is added selectively depending on the application, with an upper limit of 0.006%. B is selectively added as an element to prevent surface cracking during hot rolling, but if it exceeds 0.05%, the intergranular corrosion resistance is significantly reduced, so B is selectively added at 0.05% or less. sol Al is 0.001-0.05% as stated below
The lower limit is set at 0.001% because its inclusion has a remarkable effect on preventing surface cracking during hot rolling.
The upper limit was set at 0.005%. Taking SUS304 as an example, Figure 1 shows the incidence rate of surface defects (sludge defects and surface defects caused by inclusions) in hot-rolled coils after sol Al and hot rolling (number of sheets with defects/total number of sheets rolled). Indicates the relationship between As is clear from Fig. 1, by containing 0.001 to 0.005% Al as sol Al, the oxygen that enters from the slab surface during heating and the oxygen that originally exists in the steel are absorbed into the fine Al 2 crystal grains. It is made harmless and fixed by dispersing it as O3 . The amount of sol Al is
If it exceeds 0.005%, Al in the molten steel during casting.
is combined with oxygen in molten steel or foreign oxygen as Al 2 O 3 and precipitates in the continuous casting tundish nozzle. This results in blockage of the nozzle and makes casting very difficult. Conventionally, Al has been used together with Si as a deoxidizing agent during melting, but since Al causes nozzle clogging during continuous casting, a small amount is added to prevent it from remaining as sol Al. In the present invention,
A small amount of sol Al that does not cause nozzle clogging
It was discovered that surface flaws can be reduced by leaving . Figure 2 shows the results of a Greeble test on the effect of sol Al addition using SUS304 as an example. The components of the sample materials are shown in Table 1. 1300 each specimen
After heating to ℃ for 20 seconds and holding at this temperature for 50 seconds,
After cooling with water at a cooling rate of -100°C/min, a Greeble test was performed. As is clear from this test, the deformability of the steel of the present invention at high temperatures is very good. This is presumed to be because internal oxidation, particularly oxidation at prior γ grain boundaries, is suppressed during high temperature heating.

【表】 また、本発明によればスラブ加熱時に加熱炉内
の雰囲気中のO2濃度を0.5〜5.0%にするのが好ま
しく、この理由は、O2濃度を5.0%以上にすると、
スラブの酸化が著しくなり、これにともないスラ
ブ表面部も脆化が大きくなり、逆に0.5%以下に
すると、スラブ表層部のスケールオフ量が少なく
なり、元々スラブ表層にある欠陥が除去されにく
くなるからである。 これを実際にテストした結果を第3図に示す。
この第3図はSUS304についての加熱炉内雰囲気
中のO2濃度と冷延コイルにおける線状ヘゲ疵の
発生率(疵発生コイル数/全コイル数)%との関
係を示すものであるが、これから一般的に加熱炉
内のO2濃度が0.5〜5.0%を外れると冷延コイルで
のヘゲ疵が著しく増加すると判断される。なお、
上記テストにおいては、炉内スラブ表面温度は
1200〜1250℃とし、3.5〜4.0時間保持した。ま
た、sol Alの含有量は0.026%以下であつた。 炉内O2濃度の制御は排ガスO2濃度を検出し、
バーナ燃焼の燃料と空気比を制御することによつ
て調整できる。 (実施例) 本発明の実施例として第2表に連続鋳造で製造
されたSUS304系の本発明合金鋼を比較鋼と比較
して示す。〔O〕の影響を相殺するため、比較鋼
はAlレベルに合わせて、〔Si〕を増減した。スラ
ブ加熱温度1200〜1250℃で加熱炉内のO2濃度は
0〜8%の範囲で制御した。
[Table] Also, according to the present invention, it is preferable to set the O 2 concentration in the atmosphere in the heating furnace to 0.5 to 5.0% when heating the slab, and the reason for this is that when the O 2 concentration is 5.0% or more,
The oxidation of the slab becomes significant, and as a result, the surface of the slab becomes more brittle.On the other hand, if it is set to 0.5% or less, the amount of scale-off on the surface of the slab decreases, making it difficult to remove defects that originally exist on the surface of the slab. It is from. Figure 3 shows the results of an actual test.
This Figure 3 shows the relationship between the O 2 concentration in the atmosphere in the heating furnace and the incidence of linear sagging defects in cold rolled coils (number of coils with defects/total number of coils)% for SUS304. From this, it is generally determined that when the O 2 concentration in the heating furnace is outside of 0.5 to 5.0%, the occurrence of curling defects in cold-rolled coils increases significantly. In addition,
In the above test, the furnace slab surface temperature was
The temperature was set at 1200-1250°C and held for 3.5-4.0 hours. Moreover, the content of sol Al was 0.026% or less. The O 2 concentration inside the furnace is controlled by detecting the exhaust gas O 2 concentration,
It can be adjusted by controlling the fuel and air ratio of burner combustion. (Example) As an example of the present invention, Table 2 shows a comparison of SUS304 series alloy steel of the present invention manufactured by continuous casting with comparative steel. In order to offset the influence of [O], [Si] was increased or decreased in the comparison steel according to the Al level. The slab heating temperature was 1200 to 1250°C, and the O 2 concentration in the heating furnace was controlled within the range of 0 to 8%.

【表】【table】

【表】 このようにして加熱炉で加熱し、熱延冷却し
て、製造した冷延コイルでの線状ヘゲ疵の発生率
(疵発生コイル数/全コイル数)%を第4図に示
す。この第4図から明らかなように本発明鋼は、
ヘゲ疵を著しく低減することができる。第4図に
おいて、sol Alが0.005%より高くなると、連続
鋳造時、ノズル詰まり発生しやすく、またAl2O3
介在物が多くなり好ましくない。 (発明の効果) 本発明鋼によれば、従来熱延コイルで発見され
た疵をグラインダーで研磨除去するための工程追
加によるコストアツプを押さえることが可能にな
つた。さらに、冷延コイルでも疵発生による歩留
まり低下が大幅に低減された。
[Table] Figure 4 shows the percentage of occurrence of linear scratches (number of coils with scratches/total number of coils) in cold-rolled coils produced by heating in a heating furnace and hot rolling cooling. show. As is clear from FIG. 4, the steel of the present invention is
Scratches can be significantly reduced. In Figure 4, when sol Al is higher than 0.005%, nozzle clogging occurs easily during continuous casting, and Al 2 O 3
This is not preferable as it increases the number of inclusions. (Effects of the Invention) According to the steel of the present invention, it has become possible to suppress the increase in cost due to the addition of a process for polishing away flaws found in conventional hot rolled coils using a grinder. Furthermore, the reduction in yield due to the occurrence of defects in cold-rolled coils was significantly reduced.

【図面の簡単な説明】[Brief explanation of the drawing]

第1図はsol Al量と表面欠陥発生率との関係を
示すグラフ、第2図はグリーブルテストにおける
試片の直径減少率と試験温度との関係を示すグラ
フ、第3図は加熱炉内雰囲気中O2濃度が冷却コ
イルにおける線状ヘゲ疵におよぼす影響を示すグ
ラフ、第4図は本発明鋼と従来鋼の冷却コイルの
熱延による線状ヘゲ疵発生率を示すグラフであ
る。
Figure 1 is a graph showing the relationship between the amount of sol Al and the surface defect occurrence rate, Figure 2 is a graph showing the relationship between the diameter reduction rate of the specimen in the Greeble test and the test temperature, and Figure 3 is the graph inside the heating furnace. A graph showing the influence of O 2 concentration in the atmosphere on linear sagging defects in cooling coils. FIG. 4 is a graph showing the incidence of linear sagging defects due to hot rolling of cooling coils of the present invention steel and conventional steel. .

Claims (1)

【特許請求の範囲】 1 C:0.001〜0.20wt%(以下単に%で示す)、
Si:0.10〜5.0%、Mn:0.1〜11.0%、P:0.050%
以下、S:0.020%以下、Cr:11.0〜30.0%、
Ni:2.0〜30%、N:0.001〜0.160%、O:0.015
%以下を含有し、さらにMo:5.0%以下、Cu:
3.0%以下、Nb:1.0%以下およびSn:0.10%以下
の1種類または2種類以上と、Ti:0.05%以下、
Zr:0.10%以下、Ca:0.006%以下およびB:
0.05%以下の1種類または2種類以上を含み、か
つ、sol Alを0.001〜0.005%含有し、残部がFeお
よび不可避不純物よりなる熱間圧延で表面割れの
少ないステンレス合金鋼。 2 C:0.001〜0.20%、Si:0.10〜5.0%、Mn:
0.1〜11.0%、P:0.050%以下、S:0.020%以
下、Cr:11.0〜30.0%、Ni:2.0〜30%、N:
0.001〜0.160%、O:0.015%以下を含有し、さら
にMo:5.0%以下、Cu:3.0%以下、Nb:1.0%
以下およびSn:0.10%以下の1種類または2種類
以上と、Ti:0.05%以下、Zr:0.10%以下、Ca:
0.006%以下およびB:0.05%以下の1種類また
は2種類以上を含み、かつ、sol Alを0.001〜
0.005%含有し、残部がFeおよび不可避不純物よ
りなるステンレス合金鋼のスラブを加熱するに際
し、スラブ加熱炉の炉内雰囲気中のO2濃度を0.5
〜5.0%にすることを特徴とする熱間圧延で表面
割れの少ないステンレス合金鋼のスラブ加熱方
法。
[Claims] 1C: 0.001 to 0.20wt% (hereinafter simply expressed as %),
Si: 0.10-5.0%, Mn: 0.1-11.0%, P: 0.050%
Below, S: 0.020% or less, Cr: 11.0-30.0%,
Ni: 2.0~30%, N: 0.001~0.160%, O: 0.015
% or less, and further contains Mo: 5.0% or less, Cu:
3.0% or less, one or more types of Nb: 1.0% or less and Sn: 0.10% or less, Ti: 0.05% or less,
Zr: 0.10% or less, Ca: 0.006% or less, and B:
A stainless steel alloy steel containing 0.05% or less of one or more sol Al, and 0.001 to 0.005% of sol Al, with the balance being Fe and unavoidable impurities, and exhibits few surface cracks when hot rolled. 2 C: 0.001-0.20%, Si: 0.10-5.0%, Mn:
0.1-11.0%, P: 0.050% or less, S: 0.020% or less, Cr: 11.0-30.0%, Ni: 2.0-30%, N:
Contains 0.001 to 0.160%, O: 0.015% or less, Mo: 5.0% or less, Cu: 3.0% or less, Nb: 1.0%
One or more of the following and Sn: 0.10% or less, Ti: 0.05% or less, Zr: 0.10% or less, Ca:
Contains one or more types of 0.006% or less and B: 0.05% or less, and sol Al from 0.001 to
When heating a slab of stainless alloy steel containing 0.005% O 2 and the remainder consisting of Fe and unavoidable impurities, the O 2 concentration in the atmosphere inside the slab heating furnace is set to 0.5%.
A method for heating slabs of stainless alloy steel with less surface cracking during hot rolling, characterized by reducing the temperature to ~5.0%.
JP15255585A 1985-07-12 1985-07-12 Stainless alloy steel undergoing hardly surface cracking during hot rolling and method for heating its slab Granted JPS6213556A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP15255585A JPS6213556A (en) 1985-07-12 1985-07-12 Stainless alloy steel undergoing hardly surface cracking during hot rolling and method for heating its slab

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP15255585A JPS6213556A (en) 1985-07-12 1985-07-12 Stainless alloy steel undergoing hardly surface cracking during hot rolling and method for heating its slab

Publications (2)

Publication Number Publication Date
JPS6213556A JPS6213556A (en) 1987-01-22
JPH0448865B2 true JPH0448865B2 (en) 1992-08-07

Family

ID=15543026

Family Applications (1)

Application Number Title Priority Date Filing Date
JP15255585A Granted JPS6213556A (en) 1985-07-12 1985-07-12 Stainless alloy steel undergoing hardly surface cracking during hot rolling and method for heating its slab

Country Status (1)

Country Link
JP (1) JPS6213556A (en)

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* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
KR19990053868A (en) * 1997-12-24 1999-07-15 이구택 Hot Rolling Method for Reducing Surface Defects of Austenitic Stainless Steels
KR100435447B1 (en) * 1998-12-08 2004-09-04 주식회사 포스코 Manufacturing method of austenitic stainless hot rolled steel sheet by hot direct rolling
MX383871B (en) * 2014-05-21 2025-03-12 Jfe Steel Corp HIGH-STRENGTH SEAMLESS STAINLESS STEEL PIPE FOR TUBULAR PRODUCTS IN THE PETROLEUM REGION AND METHOD FOR MANUFACTURING SAME.

Also Published As

Publication number Publication date
JPS6213556A (en) 1987-01-22

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