JPH0543769B2 - - Google Patents
Info
- Publication number
- JPH0543769B2 JPH0543769B2 JP15255685A JP15255685A JPH0543769B2 JP H0543769 B2 JPH0543769 B2 JP H0543769B2 JP 15255685 A JP15255685 A JP 15255685A JP 15255685 A JP15255685 A JP 15255685A JP H0543769 B2 JPH0543769 B2 JP H0543769B2
- Authority
- JP
- Japan
- Prior art keywords
- less
- slab
- heating
- hot rolling
- stainless 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 - Lifetime
Links
- 238000010438 heat treatment Methods 0.000 claims description 29
- 238000005098 hot rolling Methods 0.000 claims description 21
- 238000000034 method Methods 0.000 claims description 14
- 229910001256 stainless steel alloy Inorganic materials 0.000 claims description 7
- 229910052742 iron Inorganic materials 0.000 claims description 3
- 229910052748 manganese Inorganic materials 0.000 claims description 3
- 229910001220 stainless steel Inorganic materials 0.000 claims description 3
- 239000010935 stainless steel Substances 0.000 claims description 3
- 229910052717 sulfur Inorganic materials 0.000 claims description 3
- 229910052804 chromium Inorganic materials 0.000 claims description 2
- 239000012535 impurity Substances 0.000 claims description 2
- 229910052759 nickel Inorganic materials 0.000 claims description 2
- 229910052758 niobium Inorganic materials 0.000 claims description 2
- 229910052757 nitrogen Inorganic materials 0.000 claims description 2
- 229910052718 tin Inorganic materials 0.000 claims description 2
- 229910052726 zirconium Inorganic materials 0.000 claims description 2
- 229910052760 oxygen Inorganic materials 0.000 claims 1
- 229910052698 phosphorus Inorganic materials 0.000 claims 1
- 230000007547 defect Effects 0.000 description 14
- 230000007797 corrosion Effects 0.000 description 11
- 238000005260 corrosion Methods 0.000 description 11
- 229910001566 austenite Inorganic materials 0.000 description 9
- 230000000694 effects Effects 0.000 description 9
- 238000007665 sagging Methods 0.000 description 7
- 239000000203 mixture Substances 0.000 description 6
- 239000010936 titanium Substances 0.000 description 6
- 229910000851 Alloy steel Inorganic materials 0.000 description 5
- 238000005336 cracking Methods 0.000 description 5
- 229910000963 austenitic stainless steel Inorganic materials 0.000 description 4
- XEEYBQQBJWHFJM-UHFFFAOYSA-N Iron Chemical compound [Fe] XEEYBQQBJWHFJM-UHFFFAOYSA-N 0.000 description 3
- 230000003647 oxidation Effects 0.000 description 3
- 238000007254 oxidation reaction Methods 0.000 description 3
- 229910000831 Steel Inorganic materials 0.000 description 2
- 238000005097 cold rolling Methods 0.000 description 2
- 238000009749 continuous casting Methods 0.000 description 2
- 238000001816 cooling Methods 0.000 description 2
- 239000000446 fuel Substances 0.000 description 2
- 239000010802 sludge Substances 0.000 description 2
- 238000007711 solidification Methods 0.000 description 2
- 230000008023 solidification Effects 0.000 description 2
- 239000010959 steel Substances 0.000 description 2
- 150000003568 thioethers Chemical class 0.000 description 2
- 229910000859 α-Fe Inorganic materials 0.000 description 2
- 102000004190 Enzymes Human genes 0.000 description 1
- 108090000790 Enzymes Proteins 0.000 description 1
- NINIDFKCEFEMDL-UHFFFAOYSA-N Sulfur Chemical compound [S] NINIDFKCEFEMDL-UHFFFAOYSA-N 0.000 description 1
- RTAQQCXQSZGOHL-UHFFFAOYSA-N Titanium Chemical compound [Ti] RTAQQCXQSZGOHL-UHFFFAOYSA-N 0.000 description 1
- 229910045601 alloy Inorganic materials 0.000 description 1
- 239000000956 alloy Substances 0.000 description 1
- 238000005266 casting Methods 0.000 description 1
- 238000012733 comparative method Methods 0.000 description 1
- 229910052802 copper Inorganic materials 0.000 description 1
- 238000002474 experimental method Methods 0.000 description 1
- 238000011835 investigation Methods 0.000 description 1
- 238000004519 manufacturing process Methods 0.000 description 1
- 239000000463 material Substances 0.000 description 1
- 238000002844 melting Methods 0.000 description 1
- 230000008018 melting Effects 0.000 description 1
- 150000001247 metal acetylides Chemical class 0.000 description 1
- 229910052750 molybdenum Inorganic materials 0.000 description 1
- 230000000149 penetrating effect Effects 0.000 description 1
- 238000004881 precipitation hardening Methods 0.000 description 1
- 238000012545 processing Methods 0.000 description 1
- 238000005096 rolling process Methods 0.000 description 1
- 229920006395 saturated elastomer Polymers 0.000 description 1
- 239000006104 solid solution Substances 0.000 description 1
- 239000002436 steel type Substances 0.000 description 1
- 239000011593 sulfur Substances 0.000 description 1
- 239000002344 surface layer Substances 0.000 description 1
- 229910052719 titanium Inorganic materials 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C21—METALLURGY OF IRON
- C21D—MODIFYING 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
- C21D9/00—Heat treatment, e.g. annealing, hardening, quenching or tempering, adapted for particular articles; Furnaces therefor
- C21D9/0081—Heat treatment, e.g. annealing, hardening, quenching or tempering, adapted for particular articles; Furnaces therefor for slabs; for billets
Landscapes
- 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)
- Heat Treatment Of Sheet Steel (AREA)
Description
(産業上の利用分野)
本発明は、熱間圧延前のステンレス合金鋼スラ
ブの加熱方法、特にステンレス合金鋼の熱間圧延
時に発生する小さな割れ疵に起因するヘゲ疵の発
生を少なくするためのステンレス合金鋼スラブの
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(スリーバ
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
述の欠陥は到命的であり、歩留り低下のため、大
幅なコストアツプを招いている。
上述の欠陥の理論的解明は必ずしも十分でない
が、一般的には、鋳造凝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酵素が濃化
しており、加熱中に硫化物、酸化物が生成し、こ
れが脆化を促進し、熱間圧延前に小さな割れ疵を
発生させると推定されている。
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、また、特開昭57−127506号公報に記載され
ているように、連鋳時の溶鋼加熱温度ΔT(液相
線温度と鋳造温度の差)とN値の積に応じて加熱
温度を調整する方法、Ti添加等特殊成分を添加
して熱間強度を向上させる方法が知られている。
しかし、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、耐食性を考
慮して設定されるもので、δcal値を0近傍に合せ
ることは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際
上問題がある。
また、第2の方法は、連続鋳造中ΔTおよびN
量は変化し、雑多の履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、介在物の増加により、ストリンガー疵が
増加するし、高価な特殊合金鉄添加によるコスト
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、ステンレス合金鋼の熱間圧延時に旧
オーステナイト粒界に小さな割れが発生するのを
防止するための新規な方法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、種々の実験および検討の結果、特定
組成のステンレス合金鋼スラブを、熱間圧延前
に、特定のO2濃度のスラブ加熱炉内雰囲気内で
かつ特定のスラブ表面温度および特定の保持時間
で加熱することによつて、熱間圧延時に旧オース
テナイト粒界に小さな割れが発生するのを防止す
ることができ、これによつて冷延コイルにおける
ヘゲ疵の発生を減少させ得るという事実の認識に
基づくものである。
本発明によれば、重量パーセントで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:2.0〜30.0%、N:0.001〜0.060%、
O:0.015%以下、Al:4.0%以下を含有し、さら
にMo:5.0%以下、Cu:3.0%以下、Nb:1.0%
以下、Ti:0.05%以下、Zr:0.10%以下、Ca:
0.06%以以下、Sn:0.10%以下、B:0.05%以下
の1種または2種以上を含み、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
を熱間圧延前に加熱するに際し、スラブ加熱炉内
雰囲気のO2濃度を体積パーセントで0.5〜5.0%に
制御し、さらに、スラブ表面温度をT℃、その温
度での保持時間をH時間とした場合(H+1.1)・
(T−1050)≦800になるようにスラブ加熱温度と
加熱時間を制御することを特徴とする。
通常、熱間圧延前にスラブを加熱する際、燃料
原単位を最少にするために空燃比制御で炉内O2
濃度が0%になるように制御している。しかし、
スラブ加熱炉内雰囲気のO2濃度がある領域でス
ラブ酸化は最も少なくなる。この領域以下でも以
上でもスラブ内部は鋼中のOまたは外部から侵入
したOによつて、特に旧オーステナイト粒界は内
部酸化が進み、脆化が著しくなる。これらは加熱
温度が高いほど著しい。
冷却コイル表面の線状ヘゲ疵の発生状況とスラ
ブ加熱炉内雰囲気中のO2濃度およびスラブ表面
温度との関係を、第1表に示す成分のオーステナ
イトステンレス鋼につき定量的に調査した結果の
一例を第1図に示している。
(Industrial Application Field) The present invention relates to a method for heating a stainless alloy steel slab before hot rolling, and in particular, a method for reducing the occurrence of sagging defects caused by small cracks that occur during hot rolling of stainless alloy steel. The present invention relates to a method for heating a stainless steel alloy slab. (Prior Art) One of the main surface defects that pose a problem when hot rolling stainless steel alloys is linear sludge flaws, which are usually called slivers. This defect does not disappear even after cold rolling, and in many cases
Fine sagging defects that cannot be detected in hot-rolled coils become more noticeable during cold rolling, which has become a major problem.
In stainless steel alloys, where surface quality is important, the above-mentioned defects are fatal, resulting in lower yields and a significant increase in costs. Although the theoretical elucidation of the above defects is not necessarily sufficient, it is generally believed that they are caused by embrittlement of prior austenite grain boundaries during casting and solidification. This is because sulfur and enzymes are concentrated in the prior austenite grain boundaries, and sulfides and oxides are generated during heating, which promotes embrittlement and is thought to cause small cracks to occur before hot rolling. ing. Conventionally, as a method for preventing cracking during hot rolling, as described in Japanese Patent Application Laid-Open No. 16153/1983,
δcal (calculated value of δ ferrite amount) = 3 (Cr + Mo +
1.5Si+0.5Nb)-2.8(Ni+1/2Mn+1/2Cu)-
84(C+N)-19.8 is determined by A method of adjusting the heating temperature according to the product of the N value (temperature difference) and a method of improving hot strength by adding a special component such as Ti addition is known. However, the first method attempts to suppress the calculated value δcal of δ ferrite, which is a cause of embrittlement during hot rolling, to 4.0% or less. However, in reality, the components of stainless steel alloy are determined by considering mechanical properties and corrosion resistance, and it is difficult to satisfy the δcal value close to 0 for many steel types. Furthermore, it is difficult to achieve 100% target composition during melting of stainless alloy steel, which is a practical problem. In addition, the second method is based on ΔT and N during continuous casting.
In the operation of a heating furnace where it is necessary to heat many slabs at the same time with variable amounts and miscellaneous histories, it is practically impossible to control all the slabs. Furthermore, the addition of a third special component, e.g. Ti
Addition increases stringer flaws due to an increase in inclusions, and the addition of expensive special alloy iron significantly increases costs. (Problems to be Solved by the Invention) The present invention seeks to provide a novel method for preventing the occurrence of small cracks in prior austenite grain boundaries during hot rolling of stainless alloy steel. (Means for Solving the Problems) As a result of various experiments and studies, the present invention has developed a stainless steel alloy slab having a specific composition in an atmosphere in a slab heating furnace with a specific O 2 concentration before hot rolling. Moreover, by heating the slab at a specific surface temperature and a specific holding time, it is possible to prevent small cracks from forming at prior austenite grain boundaries during hot rolling, thereby reducing the risk of cracking in cold rolled coils. This is based on the recognition of the fact that the occurrence of defects can be reduced. According to the invention, C in weight percent: 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: 2.0~30.0%, N: 0.001~0.060%,
Contains O: 0.015% or less, Al: 4.0% or less, Mo: 5.0% or less, Cu: 3.0% or less, Nb: 1.0%
Below, Ti: 0.05% or less, Zr: 0.10% or less, Ca:
When heating a slab of stainless steel alloy steel containing one or more of 0.06% or less, Sn: 0.10% or less, and B: 0.05% or less, with the balance consisting of Fe and unavoidable impurities before hot rolling, the slab If the O 2 concentration in the heating furnace atmosphere is controlled to 0.5 to 5.0% by volume, and the slab surface temperature is T°C and the holding time at that temperature is H hours (H + 1.1).
It is characterized by controlling the slab heating temperature and heating time so that (T-1050)≦800. Normally, when heating a slab before hot rolling, the air-fuel ratio is controlled to reduce O 2 in the furnace in order to minimize fuel consumption.
The concentration is controlled to be 0%. but,
Slab oxidation is minimized in a region where the O 2 concentration in the atmosphere inside the slab heating furnace is high. Whether below or above this range, internal oxidation progresses inside the slab due to O in the steel or O penetrating from the outside, particularly at prior austenite grain boundaries, resulting in significant embrittlement. These effects become more pronounced as the heating temperature increases. The relationship between the occurrence of linear scratches on the surface of the cooling coil, the O 2 concentration in the atmosphere inside the slab heating furnace, and the slab surface temperature is based on the results of a quantitative investigation of the austenitic stainless steel with the components shown in Table 1. An example is shown in FIG.
【表】【table】
【表】
第1図は、スラブ表面温度1200〜1250℃で、か
つその温度での保持時間が1.5〜3.5時間で加熱炉
内雰囲気中のO2濃度と冷延コイル表面の線状ヘ
ゲ疵初成率との関係を示す。
第1図から明らかなように、加熱炉内雰囲気中
のO2濃度は体積%で0.5〜5.0%の範囲で、線状ヘ
ゲ疵が最も少なくなる。O2濃度が0.5%未満でも
5.0%を超えても、線状ヘゲ疵発生領域が増加す
る。即ち、5%を超えると酸化が著しくなり、
0.5%未満では逆にスラブ表面層のスケールオフ
量が少なくなり、スラブ表面の欠陥が残り易いた
めである。
また、第2図は第1表のオーステナイトステン
レス鋼を用い加熱炉内雰囲気中のO2濃度を体積
%で0.5〜5.0%に制御した状態下での加熱温度と
その温度での保持時間による冷延コイル表面の線
状ヘゲ疵の発生率(疵発生コイル数/全コイル
数)を示しており、図中、記号●、×、△および
○は線状ヘゲ疵発生率31%以上、16〜30%、5〜
15%および5%未満をそれぞれ示し、また、曲線
Aは(H+1.1)・(T−1050)=800のラインを示
す。このラインAは、加熱炉内雰囲気中のO2濃
度が体積%で0.5〜5.0%のときの、線状ヘゲ疵発
生の限界ラインを示すものである。
これらの調査結果からわかるように、熱延時に
発生する線状ヘゲ疵を防止するには、加熱炉内雰
囲気中のO2濃度を重量%で0.5〜5.0%にし、か
つ、スラブ表面温度をT℃として、その温度での
保持時間をH時間とした場合、TとHを(H+
1.1)・(T−1050)≦800なる範囲になるように調
整する必要がある。
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、実用を考慮して
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、脆化の著しくなる5%以上を除去、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、加工性および
耐食性が良くなるが、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%にした。
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の点から
11.0%が下限であり、脆性の増大と加工が困難に
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%にした。
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
0.060%とし、下限は製造上の下限をもつて0.001
%とした。
Moは、耐食性向上に有効で、用途により5.0%
まで選択的できる。
Cuも、耐食性に有効であるが、加工性と、圧
延時の割れの問題から上限は3.0%とした。
Nbは、安定な炭化物を形成するため、耐食性
に有効であるが、脆化の問題から上限を1.0%と
した。
Tiは、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
添加するが、効果の飽和点0.05%をもつて上限と
する。
Zrも、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%を上限とした。
Caも同様の効果で、介在物形態制御に効果が
あるが、耐食性を劣化させるため0.06%を上限と
して、用途により選択添加する。
Snは、耐食性を向上させるため、効果の飽和
する0.10%まで用途によつて選択添加する。
Bは、熱間時の割れを防止するために添加され
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。
Alは、脱酸に有効であるが、Si、Mn等の量に
よつては不要である。さらに用途によつては析出
硬化を狙つて多量に添加する場合があり、その効
果の飽和する4.0%をもつて上限とした。
(実施例)
転炉によつて第2表に示す本発明の成分組成範
囲のステンレス合金鋼を溶製し、連続鋳造により
スラブとした。本発明方法を用いて加熱炉の制御
をした結果を第2表に示す。比較法も合せて示し
た。本表から明らかなように、本発明方法を用い
れば、熱延時に発生する線状ヘゲ疵は著しく低減
されるが、本発明の成分組成範囲内のステンレス
鋼であつても、スラブ加熱炉内雰囲気のO2濃度
が体積パーセントで0.5〜5.0%の範囲外である場
合、またはスラブ表面温度Tcおよび保持時間H
が(H+1.1)×(T−1.050)≦800の関係から外れ
る場合には熱延時に多くの線状ヘゲ疵が発生して
いる。[Table] Figure 1 shows the O 2 concentration in the atmosphere in the heating furnace and the linear sagging flaws on the surface of the cold-rolled coil when the slab surface temperature is 1200 to 1250℃ and the holding time at that temperature is 1.5 to 3.5 hours. The relationship with the initial birth rate is shown. As is clear from FIG. 1, when the O 2 concentration in the atmosphere inside the heating furnace is in the range of 0.5 to 5.0% by volume, the linear sagging defects are minimized. Even if the O2 concentration is less than 0.5%
Even if it exceeds 5.0%, the area where linear bald spots occur will increase. That is, when it exceeds 5%, oxidation becomes significant;
This is because if it is less than 0.5%, the amount of scale-off on the slab surface layer will be reduced, and defects will likely remain on the slab surface. In addition, Figure 2 shows the heating temperature and the holding time at that temperature when using the austenitic stainless steel in Table 1 and controlling the O 2 concentration in the atmosphere in the heating furnace to 0.5 to 5.0% by volume. It shows the occurrence rate of linear scratches on the surface of rolled coils (number of coils with scratches/total number of coils), and in the figure, the symbols ●, ×, △, and ○ indicate the occurrence rate of linear scratches of 31% or more, 16~30%, 5~
15% and less than 5%, respectively, and curve A shows the line of (H+1.1)·(T-1050)=800. This line A indicates the limit line for the occurrence of linear sagging defects when the O 2 concentration in the atmosphere in the heating furnace is 0.5 to 5.0% by volume. As can be seen from these survey results, in order to prevent linear sagging defects that occur during hot rolling, the O 2 concentration in the atmosphere inside the heating furnace must be set to 0.5 to 5.0% by weight, and the slab surface temperature must be If T°C is the holding time at that temperature and H hours, then T and H are (H+
1.1) It is necessary to adjust it so that it is in the range of (T-1050)≦800. Next, the reasons for limiting each component will be described. For C, the lower the better from the point of view of corrosion resistance, and the higher it is from the point of view of heat resistance, but considering practical use,
It was set at 0.001 to 0.20%. A lower Si content is better from the viewpoint of processability, but if it is too low, deoxidation will be insufficient. Therefore, the lower limit is set to 0.1%
Remove 5% or more of the material that causes significant embrittlement, and set the upper limit.
It 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%. Also,
The higher the amount, the more stable the austenite becomes, and the better the workability and corrosion resistance, but the effect reaches saturation, so it is 11.0%.
was set as the upper limit. As P increases, workability and corrosion resistance deteriorate, so the upper limit was set at 0.050%. S deteriorates hot workability. In particular, during solidification, it segregates at austenite grain boundaries and becomes the main cause of linear heave defects that occur during hot rolling. Therefore, the upper limit should be 0.020%. For O, for the same reason as S, lower is better, so the upper limit was set at 0.015%. Cr is selected from the viewpoint of corrosion resistance as a stainless steel.
The lower limit is 11.0%, and the upper limit was set at 30% in consideration of increased brittleness and difficulty in processing. Ni has a relationship with the amount of Cr, but considering this relationship and the stability of the austenite phase, it was set to 2.0% or more. The upper limit was set at 30% due to cost considerations. In the sense that N stabilizes the austenite phase,
The more the better, but the upper limit should be set considering the limit of the amount of solid solution.
0.060%, and the lower limit is 0.001 with the lower manufacturing limit.
%. Mo is effective in improving corrosion resistance, depending on the application, 5.0%
You can be selective. Cu is also effective for corrosion resistance, but the upper limit was set at 3.0% due to problems with workability and cracking during rolling. Nb forms stable carbides and is therefore effective in corrosion resistance, but due to the problem of embrittlement, the upper limit was set at 1.0%. Ti has the effect of preventing surface cracking during hot rolling by forming stable sulfides and at the same time making it fine. However, if added in large amounts, it can cause titanium stringer flaws, so it may be added in small amounts depending on the application. However, the upper limit is set at the saturation point of 0.05%. Zr also has the same effect as Ti, but the upper limit was set at 0.10% in consideration of cost and effect saturation. Ca has a similar effect and is effective in controlling the form of inclusions, but since it degrades corrosion resistance, it is added selectively depending on the application, with an upper limit of 0.06%. In order to improve corrosion resistance, Sn is selectively added up to 0.10%, which saturates the effect, depending on the application. B is added to prevent cracking during hot heating, but if it exceeds 0.05%, the intergranular corrosion resistance will be significantly reduced, so it is selectively added at 0.05% or less. Al is effective for deoxidation, but is not necessary depending on the amount of Si, Mn, etc. Furthermore, depending on the application, a large amount may be added to achieve precipitation hardening, and the upper limit was set at 4.0%, at which the effect is saturated. (Example) Stainless alloy steel having the composition range of the present invention shown in Table 2 was melted in a converter and made into a slab by continuous casting. Table 2 shows the results of controlling the heating furnace using the method of the present invention. Comparative methods are also shown. As is clear from this table, if the method of the present invention is used, linear scratches that occur during hot rolling can be significantly reduced, but even if stainless steel is within the composition range of the present invention, If the O2 concentration in the internal atmosphere is outside the range of 0.5-5.0% by volume, or the slab surface temperature Tc and holding time H
If it deviates from the relationship of (H+1.1)×(T-1.050)≦800, many linear flaws have occurred during hot rolling.
【表】【table】
【表】【table】
【表】
(発明の効果)
本発明方法により、熱延による線状ヘゲ疵が著
しく低減され、この結果冷却コイルの歩留りが著
しく向上した。また、熱延後に、熱延コイル表面
の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できる。[Table] (Effects of the Invention) According to the method of the present invention, linear scratches due to hot rolling were significantly reduced, and as a result, the yield of cooling coils was significantly improved. Moreover, it is possible to suppress the increase in cost due to the addition of a process for removing flaws on the surface of the hot-rolled coil using a grinder after hot-rolling.
第1図は本発明の特定成分組成範囲のオーステ
ナイトステンレス鋼の冷延コイルにおける線状ヘ
ゲ疵の発生率と熱延加熱炉内雰囲気中のO2濃度
との関係を示すグラフ、
第2図は本発明の特定成分組成範囲のオーステ
ナイトステンレス鋼のスラブの熱延前加熱表面温
度と保持時間とが冷延コイル表面の線状ヘゲ疵発
生におよぼす影響度を示すグラフである。
FIG. 1 is a graph showing the relationship between the incidence of linear sagging defects and the O 2 concentration in the atmosphere in the hot-rolling furnace in a cold-rolled coil of austenitic stainless steel having a specific composition range according to the present invention. 1 is a graph showing the degree of influence of the pre-hot rolling heating surface temperature and holding time of a slab of austenitic stainless steel having a specific composition range of the present invention on the occurrence of linear sludge defects on the surface of a cold rolled coil.
Claims (1)
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:
2.0〜30.0%、N:0.001〜0.060%、O:0.015%以
下、Al:4.0%以下を含有し、さらにMo:5.0%
以下、Cu:3.0%以下、Nb:1.0%以下、Ti0.05
%以下、Zr:0.10%以下、Ca:0.06%以下、Sn:
0.10%以下、B:0.05%以下の1種または2種以
上を含み、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熱間圧延前に加熱
するに際し、スラブ加熱炉内雰囲気のO2濃度を
体積パーセントで0.5〜5.0%に制御し、かつ、ス
ラブ表面温度をT℃、その温度での保持時間をH
時間とした場合(H+1.1)・(T−1050)≦800に
なるようにスラブ加熱温度と加熱時間を制御する
ことを特徴とするステンレス合金鋼スラブの加熱
方法。1 C: 0.001-0.20%, Si: in weight percent
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:
Contains 2.0 to 30.0%, N: 0.001 to 0.060%, O: 0.015% or less, Al: 4.0% or less, and further Mo: 5.0%.
Below, Cu: 3.0% or less, Nb: 1.0% or less, Ti0.05
% or less, Zr: 0.10% or less, Ca: 0.06% or less, Sn:
When heating a stainless steel slab containing one or more of B: 0.10% or less, B: 0.05% or less, and the remainder consisting of Fe and unavoidable impurities before hot rolling, O 2 in the atmosphere in the slab heating furnace The concentration is controlled to 0.5 to 5.0% by volume, and the slab surface temperature is T℃ and the holding time at that temperature is H.
A method for heating a stainless steel alloy slab, characterized by controlling the slab heating temperature and heating time so that (H+1.1)·(T-1050)≦800 when expressed as time.
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP15255685A JPS6213527A (en) | 1985-07-12 | 1985-07-12 | Method for heating stainless alloy steel slab |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP15255685A JPS6213527A (en) | 1985-07-12 | 1985-07-12 | Method for heating stainless alloy steel slab |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| JPS6213527A JPS6213527A (en) | 1987-01-22 |
| JPH0543769B2 true JPH0543769B2 (en) | 1993-07-02 |
Family
ID=15543051
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP15255685A Granted JPS6213527A (en) | 1985-07-12 | 1985-07-12 | Method for heating stainless alloy steel slab |
Country Status (1)
| Country | Link |
|---|---|
| JP (1) | JPS6213527A (en) |
Families Citing this family (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| CN106414785B (en) * | 2014-05-21 | 2018-10-09 | 杰富意钢铁株式会社 | Oil well high-strength stainless steel seamless steel tube and its manufacturing method |
-
1985
- 1985-07-12 JP JP15255685A patent/JPS6213527A/en active Granted
Also Published As
| Publication number | Publication date |
|---|---|
| JPS6213527A (en) | 1987-01-22 |
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