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JPS6015684B2 - Method for manufacturing hot rolled steel materials - Google Patents
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JPS6015684B2 - Method for manufacturing hot rolled steel materials - Google Patents

Method for manufacturing hot rolled steel materials

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Publication number
JPS6015684B2
JPS6015684B2 JP5488077A JP5488077A JPS6015684B2 JP S6015684 B2 JPS6015684 B2 JP S6015684B2 JP 5488077 A JP5488077 A JP 5488077A JP 5488077 A JP5488077 A JP 5488077A JP S6015684 B2 JPS6015684 B2 JP S6015684B2
Authority
JP
Japan
Prior art keywords
scale
steel
less
steel materials
heating
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
JP5488077A
Other languages
Japanese (ja)
Other versions
JPS53140219A (en
Inventor
進 合田
正雄 上田
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.)
Nippon Steel Corp
Original Assignee
Nippon 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 Nippon Steel Corp filed Critical Nippon Steel Corp
Priority to JP5488077A priority Critical patent/JPS6015684B2/en
Publication of JPS53140219A publication Critical patent/JPS53140219A/en
Publication of JPS6015684B2 publication Critical patent/JPS6015684B2/en
Expired legal-status Critical Current

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Description

【発明の詳細な説明】 本発明は熱間圧延によるキルド鋼材特に一次スケール癖
のすくない溶接構造用圧延鋼材ならびに高張力鋼材の製
造方法に関するものである。
DETAILED DESCRIPTION OF THE INVENTION The present invention relates to a method for producing killed steel materials by hot rolling, particularly rolled steel materials for welded structures with little primary scale tendency, and high-strength steel materials.

一般にSiキルド鋼あるいは山一Siキルド鋼を用いて
製造される前記溶接構造用圧延鋼材についてはスケール
庇をできる限りすくなくすることが要望されており、特
に圧延のままで使用される形鋼などはスケール癖のない
ことが切望されている。しかしながら前記形鋼を例にと
った場合、SiあるいはN−Siキルド鋼で製造される
ため、とかくスケール癖が発生し易く、Si,山の含有
量が多くなるほどスケール剥離性が悪くなりスケール波
が多発するため、このスケール癖を減少させる方法が研
究されてきたが、工業上生産ラインで採用できるほどの
経済的な方法は確立されておらず、スケール癖の発生に
悩まされるのが現状であった。さて前記スケール癖の発
生がすくなく、しかも経済的な製造方法の研究を行なっ
た本発明者等はまずスケールの剥離性に着目した結果、
該剥離性は周知のように港車テストなどによる単なるス
ケール上層部の剥離性のみに注意すべきものではなく、
スケール/地鉄境界層をなす混合層およびサブスケール
の剥離性をも考慮しなければならないことを知った。前
記スケール上層部の剥離性あるいは残留スケールに関す
る研究には周知のようにロールズ(R.ROlls)の
論文があるが、これには前記混合層およびサブスケール
の剥離性についての記述に乏しく、本発明等の知る限り
では、Sio.25%以上の高Si含有鋼などについて
いまだ工業的に成功したとの報告はない。
In general, it is desired that the scale eaves be minimized as much as possible for the rolled steel materials for welded structures manufactured using Si killed steel or Yamaichi Si killed steel. It is strongly desired that there is no scale habit. However, when we take the above-mentioned section steel as an example, since it is manufactured from Si or N-Si killed steel, it tends to cause scale problems, and the higher the content of Si and peaks, the worse the scale peelability becomes and the scale waves. Since it occurs frequently, research has been conducted on methods to reduce this scale problem, but no method has been established that is economical enough to be adopted on industrial production lines, and the current situation is that scale problems are a problem. Ta. The inventors of the present invention, who have conducted research on an economical manufacturing method that reduces the occurrence of the aforementioned scale habit, first focused on the removability of scale, and as a result,
As is well known, the removability is not only the removability of the upper layer of the scale based on port car tests.
We learned that we must also consider the mixed layer that forms the scale/substrate boundary layer and the peelability of subscales. Research on the releasability of the upper layer of scale or residual scale includes a well-known paper by R. ROlls, but this paper lacks a description of the releasability of the mixed layer and subscale, and the present invention To the best of our knowledge, Sio. There have been no reports of industrial success with high Si content steel of 25% or more.

さて、前記スケールには大別して一次スケールと二次ス
ケールの二種があり、前者は加熱工程で主として発生す
るため、黒灰色を呈する部厚し、ものとなりこれが付着
したまま圧延されると第1図に示すように雲形のスケー
ル庇15となって鋼材表面の外観を著しく害する。
Now, there are two types of scale, primary scale and secondary scale.The former mainly occurs during the heating process, so it becomes black and gray in thickness, and if it is rolled with this adhered, it will cause the first scale. As shown in the figure, a cloud-shaped scale eaves 15 is formed, which significantly impairs the appearance of the steel surface.

Siキルド、AI−Siキルド鋼は、前記一次スケール
の発生が著しいことが特色である。前記二次スケールは
熱間圧延末期以降に発生し、薄い青灰色あるいは赤灰色
を呈し、外観を損ねるものであるが、而して本発明は一
次スケールに起因する庇発生の防止を要点とするもので
、本発明では二次スケール癖については技術範囲に含ま
ない。
Si-killed steel and AI-Si killed steel are characterized by the remarkable occurrence of the primary scale. The secondary scale occurs after the end of hot rolling, exhibits a pale blue-gray or reddish-gray color, and impairs the appearance. Therefore, the main point of the present invention is to prevent the formation of eaves caused by the primary scale. Therefore, the technical scope of the present invention does not include secondary scale behavior.

さて、スケール特に一次スケールの剥離性が悪くなる要
因としては次の【1}〜【41項が知られている。
Now, the following items [1} to [41] are known as factors that worsen the peelability of scale, especially primary scale.

‘1’ 合金成分の含有量の増加。‘1’ Increase in content of alloying components.

■ スケール/池鉄境界層における合金元素(Si,C
r,Ni,CリAs,Sn等)の富化。
■ Alloying elements (Si, C) in the scale/iron boundary layer
Enrichment of r, Ni, C, As, Sn, etc.).

糊 加熱時の合金成分(FeS,Fe2Si04,Mo
o3,NiS2,V2Q等)の溶融。‘4)溶融合金成
分の粒界侵入による複雑な混合層の形成。
Glue Alloy components during heating (FeS, Fe2Si04, Mo
o3, NiS2, V2Q, etc.). '4) Formation of a complex mixed layer due to grain boundary penetration of molten alloy components.

さて、前記各項目について研究した結果、本発明者等は
特にSiについて注意を払わねばならぬことを知った。
Now, as a result of researching each of the above items, the inventors of the present invention have learned that particular attention must be paid to Si.

つまりSiは前記m〜■項に該当するうえに特に120
0qo以上の高温になるとSiがスケール/地鉄境界層
に富化して鉄酸化物Fe○と合金成分を作り、Feぶi
04(Fa鱗lite)を生成し、前記Fe2Si04
の融点は12060附近であるため、それ以上の温度に
加熱した場合、境界層に富化したFe2Si04が熔融
し、第2図のスケールと地鉄の境界層を撮った顕微鏡写
真に示すように粒界に侵入し、あたかも裸16のような
形で、スケールの固着性を高めるほか、溶融物が接着剤
のような作用をするものと推定されているからで、また
このほか熔融物がスケール生長に必要な酸素の侵入を妨
害して剥離性を阻害するとの推定もなされており、まず
このFe2Sj04の問題解決を指向すると共にAIに
ついての研究も行なった、と云うのはAIはSiと共に
脱酸剤並びに材質改質村として重要な成分であり、Si
と山は共存する機会が非常に多いためでAIが存在する
とM203が生成し、このM203とFe○との共晶物
の融点は1330q○と高いものの、地鉄およびスケー
ルを粘〈すると共にSiと重合して剥離性を阻害すると
推定されるからである。さて、前述のような門題点を解
決する周知方法としては、【a} Sjの富化を抑制す
る方法。
In other words, Si corresponds to the above m to ■ terms, and especially 120
When the temperature is higher than 0qo, Si enriches in the scale/substrate boundary layer and forms an alloy component with iron oxide Fe○,
04 (Fa scale lite) and the Fe2Si04
The melting point of is around 12060, so if it is heated to a temperature higher than that, the Fe2Si04 enriched in the boundary layer will melt and form grains as shown in the micrograph of the scale and the boundary layer of the steel in Figure 2. This is because in addition to increasing the adhesion of scale in a form similar to that of a naked 16, the melt is estimated to act like an adhesive, and in addition, the melt may cause scale growth. It has been speculated that this inhibits the penetration of oxygen, which is necessary for Fe2Sj04, and inhibits its releasability.First of all, we aimed to solve this problem with Fe2Sj04, and also conducted research on AI. It is an important component as an agent and material modification agent, and
M203 is generated when AI exists, and although the melting point of the eutectic of M203 and Fe○ is as high as 1330q○, it does not viscous the base iron and scale, but also makes Si. This is because it is presumed that it polymerizes with the metal and inhibits the releasability. Now, as a well-known method for solving the above-mentioned problems, there is a method of suppressing the enrichment of [a} Sj.

【b)Fe2Si04の溶融を避ける方法。[b) Method of avoiding melting of Fe2Si04.

‘c} 鋼材中にFe2SiQの分散を計る方法。の三
方法が考えられてきた。Siの富化を抑制する手段とし
ては、被加熱材の表面に塗料を塗布して加熱する方法が
あるが、材料費および処理費が嵩むので、特別な高級鋼
材は別として、経済性がないため、酸化を抑制する方法
、つまり加熱に際して比較的低空気比で燃焼させる手段
が採用されてきた。またそのほか前述のように低温加熱
法によってFe2Si04の溶遊を避ける手段や冷鋼片
の表面をフカーフイングすることにより、表面のSiを
鋼片中に分散させる方法も行なわれてきた。しかしなが
ら、いずれの方法も、実用性あるいは経済性の点で問題
があった。
'c} Method for measuring the dispersion of Fe2SiQ in steel materials. Three methods have been considered. One way to suppress Si enrichment is to apply paint to the surface of the material to be heated and heat it, but it is not economical, except for special high-grade steel materials, because the material and processing costs increase. Therefore, methods have been adopted to suppress oxidation, that is, to burn at a relatively low air ratio during heating. In addition, as mentioned above, methods have been used to avoid melting of Fe2Si04 by low-temperature heating, and to disperse Si on the surface into the steel billet by calfing the surface of the cold billet. However, both methods have problems in terms of practicality or economy.

而して、本発明者等は前述の如き問題点のない製造方法
を研究した結果、極めて実用的かつ経済性に富む本発明
の製造方法を開発したもので、その要旨は「CO.05
〜0.60%、Nho.5〜2.0%、Sio.25〜
0.60%、No.05%以下、PO.03%以下、S
O.03%以下、残部がFeと不可避不純物からなる鋼
材を、加熱炉の均熱帯において酸素濃度を2〜8%とし
1250qo超〜1320q0未満の温度領域において
10〜8粉ご間均熱したのち、通常の熱間圧延を行なう
熱間圧延鋼材の製造方法」にある。
As a result of research into a manufacturing method that does not have the above-mentioned problems, the present inventors have developed the extremely practical and economical manufacturing method of the present invention, the gist of which is "CO.05
~0.60%, Nho. 5-2.0%, Sio. 25~
0.60%, No. 05% or less, PO. 03% or less, S
O. 03% or less, the balance being Fe and unavoidable impurities, is soaked for 10 to 8 powders in a temperature range of more than 1250 qo to less than 1320 q0 at an oxygen concentration of 2 to 8% in the soaking zone of a heating furnace, and then ``Method for manufacturing hot rolled steel material by hot rolling.''

次に、本発明の方法を図に従って詳細に説明する。Next, the method of the present invention will be explained in detail with reference to the drawings.

第3図は鋼材の加熱に用いられる周知の加熱炉の概略縦
断面であって、予熱帯1,加熱帯2,均熱帯3からなる
多帯式加熱炉を示し、4a〜4pは加熱バーナー、5は
被加熱材(以下単に鋼材と云う)、6は煙道、7a〜7
cは酸素メーターである。辞して前記加熱炉は予熱帯と
加熱帯が一体となった形式のものであっても、本発明の
方法を適用することができる。さて鋼材5は矢印8の方
向から図示していないプッシャ−によって加熱炉中に押
し込まれるか、あるいはウオーキングビームによって装
入され、加熱バーナー4a〜4pによる子熱、加熱およ
び均熱の各工程を経て抽出口9から抽出され圧延工程に
送られる。本発明者等は従来のような低空気比つまり理
論空気量を1.0部付近とし雰囲気中の自由酸素の低い
燃焼制御をやめて、主として均熱帯3における加熱バー
ナー4c,4n,4o,4pの空気比を1.1〜1.4
と変化させて、雰囲気中の自由酸素濃度を2〜10%と
することにより、積極的にスケールの生成を行なわせ、
しかるのちデスケーリングを含む通常の熱間圧延即ち粗
、仕上圧延を行ない、スケール舵の発生率と前記自由酸
素濃度との対比を行なった結果、従来スケール癖の発生
が必らずしも減らないと信じられていた高空気比の燃焼
制御による高い自由酸素濃度の雰囲気がむしろスケール
癖発生を少なくすると云う新知見を得た。
FIG. 3 is a schematic vertical cross section of a well-known heating furnace used for heating steel materials, and shows a multi-zone heating furnace consisting of a pre-heating zone 1, a heating zone 2, and a soaking zone 3, and 4a to 4p are heating burners; 5 is a material to be heated (hereinafter simply referred to as steel material), 6 is a flue, and 7a to 7
c is an oxygen meter. In other words, the method of the present invention can be applied even if the heating furnace is of a type in which a pre-heating zone and a heating zone are integrated. Now, the steel material 5 is pushed into the heating furnace from the direction of the arrow 8 by a pusher (not shown) or charged by a walking beam, and undergoes the steps of subheating, heating, and soaking by the heating burners 4a to 4p. It is extracted from the extraction port 9 and sent to the rolling process. The present inventors stopped the conventional combustion control with a low air ratio, that is, a theoretical air amount of around 1.0 parts, and low free oxygen in the atmosphere, and mainly controlled the heating burners 4c, 4n, 4o, and 4p in the soaking zone 3. Air ratio 1.1-1.4
By changing the free oxygen concentration in the atmosphere to 2 to 10%, scale is actively generated.
After that, normal hot rolling including descaling, that is, rough and finish rolling, was performed, and as a result of comparing the occurrence rate of scale rudders and the above-mentioned free oxygen concentration, it was found that the occurrence of conventional scale defects did not necessarily decrease. We obtained new knowledge that an atmosphere with a high free oxygen concentration due to combustion control with a high air ratio actually reduces the occurrence of scale formation, which was believed to be the case.

即ち第4図に示す通り横軸に空気比と自由酸素濃度(%
)をとり、縦軸にスケール癖発生率をとった場合、折線
10に示すように空気比1.1附近からスケール癖発生
率は激減し、空気比1.4〆上でもスケール癖の発生は
ほとんど見られない。この結果から明らかなように自由
酸素濃度の最も好ましい範囲は2〜8%であることが判
る。つまり自由酸素濃度は9〜10%と多くしても良い
が、加熱が不均一になるうえスケール生成量をいたずら
に多くすることは経済性を矢ない、また2%以下ではス
ケール庇防止が安定しないので、本発明では自由酸素濃
度(以下単に酸素濃度と云う)を2〜8%と限定するも
のである。また本発明者等の数多くの実験によれば、灼
熱帯に加えて子熱帯および加熱帯の酸素濃度も2〜8%
としても良いことが判ったが、加熱効率、生産性、スケ
ール生成量の点から酸素濃度をあまり上げることは経済
性の点でやや不利となるため、予熱帯、加熱帯の酸素濃
度を低くする、つまり空気比を1.0附近とする燃焼制
御を行ない、均熱帯のみを酸素濃度2〜8%に保って操
業したが、スケール癖についてはやはり良い成績を収め
ることができ、生産性を落さなくて済んだ。さて、前記
折線10は均熱帯の温度が129000の場合であり、
温度を1260q0とした場合を折線11、1320q
oの場合を折線12、1350ooの場合を折線14、
また温度が122000の場合を折線13で示す、図か
ら明らかなように温度は122000より低くとも、ま
た1350午○より高くともスケール癖の発生が多いこ
とが判る。
That is, as shown in Figure 4, the horizontal axis shows the air ratio and free oxygen concentration (%).
), and the scale occurrence rate is plotted on the vertical axis, as shown by broken line 10, the scale occurrence rate decreases sharply from around the air ratio of 1.1, and even above the air ratio of 1.4, the scale occurrence does not occur. Almost never seen. As is clear from this result, the most preferable range of free oxygen concentration is 2 to 8%. In other words, the free oxygen concentration may be increased to 9 to 10%, but heating will become uneven and unnecessarily increasing the amount of scale generated will not be economical, and if it is less than 2%, the prevention of scale eaves will be stable. Therefore, in the present invention, the free oxygen concentration (hereinafter simply referred to as oxygen concentration) is limited to 2 to 8%. Furthermore, according to numerous experiments conducted by the present inventors, the oxygen concentration in the tropical zone and the tropical zone in addition to the scorching zone is 2 to 8%.
However, in terms of heating efficiency, productivity, and scale generation, increasing the oxygen concentration too much is economically disadvantageous, so the oxygen concentration in the preheating zone and heating zone should be lowered. In other words, we performed combustion control with an air ratio of around 1.0, and operated by keeping only the soaking zone at an oxygen concentration of 2 to 8%, but we were still able to achieve good results in terms of scaling, and this did not reduce productivity. I didn't have to. Now, the broken line 10 is when the temperature in the soaking zone is 129,000,
When the temperature is 1260q0, broken lines 11 and 1320q
The case of o is broken line 12, the case of 1350oo is broken line 14,
Further, the case where the temperature is 122,000 is shown by the broken line 13. As is clear from the figure, scale formation occurs frequently even when the temperature is lower than 122,000 and higher than 1,350 pm.

本発明者等の経験によるとこの温度の下限は1250o
o超で上限は132000未満であった。つまり125
000未満ではスケールの生成が不充分であり、また1
320ooを越えるとスケールの溶融が生じともにスケ
ールの剥離性が向上しないためと思われる。前記温度は
鋼材に接近した炉壁の温度測定計による測定値をパィロ
メーターによる鋼材の温度測定値によって補正して求め
た値である。
According to the experience of the present inventors, the lower limit of this temperature is 1250o.
o and the upper limit was less than 132,000. That is 125
If it is less than 1,000, scale generation is insufficient, and if it is less than 1,
This seems to be because if it exceeds 320 oo, the scale will melt and the peelability of the scale will not improve. The temperature is a value obtained by correcting the value measured by a temperature meter on the furnace wall close to the steel material by the temperature value measured on the steel material by a pyrometer.

操業中の加熱炉において鋼材に直接接触し、連続的にそ
の温度を計る方法は現在のところ知られていないが前記
手段あるいは炉温のみかもし〈はパィロメーターによる
榎U温又はそれに類似した測定手段を採用すれば充分目
的を達成することが出来る。次に均熱帯における均熱時
間とスケール癖の発生率を第5図に示す。第5図は横軸
に均熱帯における鋼材の滞留時間換言すると均熱時間(
分)をとり、縦軸にスケール庇発生率(%)をとったも
ので、前述のように酸素濃度を2〜8%としても、あま
り灼熱時間が短いとスケール庇の減少に対して効果がう
すし、ことが判る。
At present, there is no known method of directly contacting the steel material in an operating heating furnace and continuously measuring its temperature, but the method described above or the furnace temperature is the only method available. If adopted, the objective can be achieved. Next, Figure 5 shows the soaking time in the soaking zone and the incidence of scale formation. In Figure 5, the horizontal axis indicates the residence time of steel in the soaking zone, or in other words, the soaking time (
minutes) and scale eaves occurrence rate (%) on the vertical axis.As mentioned above, even if the oxygen concentration is 2 to 8%, if the burning time is too short, it will not be effective in reducing scale eaves. It's faint, I can see it.

即ちすくなくとも10分間以上が望ましい、しかしなが
ら灼熱時間をあまりにも長くすることは生産性および省
エネルギーの点で望ましくないうえに、かえってスケー
ル癖発生率を助長する煩向を示すので通常は10〜80
分間程度とすることが好ましい。さらに加熱炉中での鋼
材の在炉時間についてスケール癖発生率との相互関係を
研究した結果を第6図に示す。第6図は機軸に在炉時間
(時)をとり、縦軸にスケール癖発生率(%)をとった
ものであるが、在炉時間が5時間を越えるとスケール癖
の発生率が増加する煩向にあるので、本発明の方法を実
施する場合にも在炉時間は5時間を越えないように留意
した方がよい。次に、加熱炉における雰囲気ガスの組成
について説明する。本発明者等の行なった前述の第4図
〜第6図の実施例における加熱炉での酸素を除く雰囲気
ガスの組成は日208〜25%、C027〜15%、S
02300脚m以下、残部はN2であった、ところでH
20,C02,S02は酸素(02)と同様に酸化力を
有し、温度の上昇と共にほぼ02に近い酸化力を発揮す
るけれども前途の含有量範囲ではスケール癖に結びつく
ような影響力がうすく、スケール生成にあたってその作
用は02の作用とは異なるように思われる。
That is, it is desirable that the heating time be at least 10 minutes or longer.However, excessively long burning time is not only undesirable in terms of productivity and energy saving, but also tends to increase the rate of scale formation.
It is preferable to set it to about minutes. Furthermore, Fig. 6 shows the results of a study on the correlation between the time the steel material spent in the heating furnace and the scale occurrence rate. Figure 6 shows the furnace time (hours) on the axis and the scale occurrence rate (%) on the vertical axis, and the scale occurrence rate increases when the furnace time exceeds 5 hours. Therefore, when implementing the method of the present invention, care should be taken to ensure that the furnace time does not exceed 5 hours. Next, the composition of the atmospheric gas in the heating furnace will be explained. The composition of the atmospheric gas excluding oxygen in the heating furnace in the above-mentioned embodiments shown in FIGS.
Less than 02,300 leg m, the rest was N2, by the way, H
20, C02, and S02 have oxidizing power similar to oxygen (02), and as the temperature rises, they exhibit an oxidizing power close to that of 02, but in the content range in the future, their influence that leads to scale habit is weak, Its effect on scale generation appears to be different from that of 02.

その理由は詳かではないが本発明における雰囲気ガス組
成としては022〜8%に加えて、&030%以下およ
び/もしくはC0220%以下と残部N2からなる燃焼
雰囲気であれば良い。ただしS02についてはいずれの
場合も100の伽以下であることが好ましい。さて、前
述のように加熱炉において圧延温度に達した鋼材は、通
常のエッジング圧延あるいは上下方向のスケール割り込
み圧延を経て、100〜200kg/地の高圧デスケー
リング水によって上層のスケールが剥離され、ついで圧
下、デスケーリングの繰返いこよって残留スケールが剥
離される。
Although the reason for this is not clear, the atmosphere gas composition in the present invention may be a combustion atmosphere consisting of 022 to 8%, and 030% or less and/or CO2 20% or less, with the balance being N2. However, S02 is preferably 100 or less in any case. Now, as mentioned above, the steel material that has reached the rolling temperature in the heating furnace undergoes normal edging rolling or vertical scale cutting rolling, and then the upper layer of scale is removed by high-pressure descaling water of 100 to 200 kg/ground, and then the upper layer of scale is removed. Residual scale is peeled off by repeated rolling and descaling.

而して、本発明者等の推定では、スケールの剥雛性が前
述のように向上し、スケール庇が減少する理由は従来ス
ケール/地鉄境界層に富化して剥離性を阻害するといわ
れて来た合金化合物が、本発明における02条件と温度
条件下においてスケール中への分散量を増し、また残部
は上層スケール剥離後もサブスケールの酸化膨張力が旺
盛で密着力以上の剥離力が働らくのであたかも低Si鋼
と同様の良好なスケール剥離をすることにあると思われ
る。次に本発明における成分の限定理由について説明す
る。
Accordingly, the present inventors estimate that the reason why the scale peelability improves as described above and the scale eaves decrease is because it is said that the scale is enriched in the scale/substrate boundary layer and inhibits the peelability. The resulting alloy compound increases the amount of dispersion into the scale under the 02 conditions and temperature conditions of the present invention, and the remaining part has a strong oxidation expansion force in the subscale even after the upper layer peels off, and a peeling force greater than the adhesion force is exerted. It is thought that the reason for this is that it is easy to peel off scale, just like low-Si steel. Next, the reasons for limiting the components in the present invention will be explained.

本発明の対象の鋼種は前述のようにSjキルドあるいは
N−Siキルド鋼であって、用途としては主として溶接
構造用圧延鋼材ならびに高張力鋼材を対象とする。而し
て各成分元素は該鋼材の物理通および化学的性能を維持
するためのもので、その成分範囲の限定理由は次の通り
である。
As mentioned above, the steel type to which the present invention is applied is Sj killed or N-Si killed steel, and is mainly intended for use in rolled steel materials for welded structures and high-strength steel materials. Each component element is used to maintain the physical and chemical performance of the steel, and the reason for limiting the range of the components is as follows.

Cは強度を増加させるために必要であるが含有量が多く
なり0.60%以上となると延性を害するので0.60
%以下とする。
C is necessary to increase strength, but if the content increases and exceeds 0.60%, it will impair ductility, so 0.60%
% or less.

逆に0.05%以下になると強度が充分に得られないの
で下限は0.05%とする。Mnは強度靭性向上効果の
大きい元素であり、Mn○のような酸化物になってもス
ケール中に固溶し癖発生などの原因とはなり難いが、2
,0%以*上になると靭性が急激に低下して問題があり
、また0.5%以下になると強度が得られない。Siは
機械的性質を均一化するため必要であるが0.25%以
下では強度が出に〈くなることと、スケール癖発生がす
くないことから0.25%を下限とするもので、また0
.6%以上では靭性が急激に低下するので上限は0.6
%とする。AIは鋼の結晶を級粒化し靭性を向上せしめ
るのに効果があるが、0.05%を超えると介在物を生
成し易くなるため0.05%以下がよい、しかし下限に
ついてはごく徴量でも、それなりの効果があり、またS
iキルドのように意図的に添加しない場合もあり、下限
については特に限定しない。
On the other hand, if the content is less than 0.05%, sufficient strength cannot be obtained, so the lower limit is set to 0.05%. Mn is an element that has a great effect on improving strength and toughness, and even if it becomes an oxide like Mn○, it is unlikely to become a solid solution in the scale and cause problems, but 2
, 0%* or more, there is a problem in that the toughness rapidly decreases, and if it is less than 0.5%, no strength can be obtained. Si is necessary to make mechanical properties uniform, but if it is less than 0.25%, the strength will be poor and scale will be less likely to occur, so 0.25% is the lower limit.
.. If it exceeds 6%, the toughness will drop sharply, so the upper limit is 0.6.
%. AI is effective in grading steel crystals and improving toughness, but if it exceeds 0.05%, inclusions tend to form, so it is best to keep it at 0.05% or less, but the lower limit is very limited. However, it has some effect, and S
In some cases, such as in i-killed, it is not added intentionally, and the lower limit is not particularly limited.

Pはキルド鋼材としては少ないほうが良く、0.03%
以上多くなると表面癖が発生し易くなり、鋤性ならびに
延性の面で問題が生ずる。SはFeS,C船,NiS2
など低融点硫化物を作り高温脆性を起し易くまた轍性を
悪化させるので、少ないほど良い元素であるが、0.0
3%以下の含有量であれば本発明において問題になるこ
とはない。
The lower the P content for killed steel, the better, 0.03%.
If the amount exceeds this amount, surface roughness tends to occur, causing problems in terms of plowability and ductility. S is FeS, C ship, NiS2
The less the element, the better, as it creates low-melting point sulfides such as sulfides, which tend to cause high-temperature brittleness and worsen rutting.
If the content is 3% or less, there will be no problem in the present invention.

而して、本発明を適用した鋼材の成分とスケール癖の減
少率に関する実施例を次の第1表に示す。
Examples regarding the composition and scale reduction rate of steel materials to which the present invention is applied are shown in Table 1 below.

第1表 第1表中のスケール癖減少率とは、通常の低空気比燃焼
制御を行なって加熱後圧延した鋼材のうち癖の発生した
鋼材数と本発明による製造法で製造した鋼材のうち癖の
発生した鋼材数とを比較しその減少率を云うものである
Table 1 The scale reduction rate in Table 1 is calculated based on the number of steel products with scale defects among the steel products heated and rolled using normal low air ratio combustion control, and the number of steel products produced by the manufacturing method according to the present invention. This is the reduction rate by comparing the number of steel materials with defects.

前述のように溶接構造用鋼に適用し、スケール癖の減少
について効果が認められたので、さらにC,S;,Mn
の含有量の高い高強度あるいは高硬度鋼材について試験
を行なった結果、第2表に示す通り好結果を得た。
As mentioned above, it was applied to welded structural steel and was found to be effective in reducing scale habit, so C, S;, Mn
As a result of conducting tests on high-strength or high-hardness steel materials with a high content of , good results were obtained as shown in Table 2.

この原因はC,Mnなどはガス化またはスケール中への
固溶性が良く剥離阻害因子とならないからであると思わ
れる。第2表 本発明者等は前述のような成分の鋼材について良好な成
績をおさめたが、前記成分に加えて、Cu,V,Ni,
Cr,Nb,Ti,Zr,Mo,Rem等を少量添加し
た鋼材についても効果が認められる。
The reason for this is thought to be that C, Mn, etc. have good solid solubility in gasification or scale and do not become a factor that inhibits peeling. Table 2 The present inventors have achieved good results with steel materials having the above-mentioned components, but in addition to the above-mentioned components, Cu, V, Ni,
The effect is also recognized in steel materials to which small amounts of Cr, Nb, Ti, Zr, Mo, Rem, etc. are added.

以上詳細に説明したように本発明の方法はSiもしくは
N−Siキルド鋼材についてスケ−ル庇の発生を激減せ
しめうる有用な製造法である。
As explained in detail above, the method of the present invention is a useful manufacturing method that can drastically reduce the occurrence of scale eaves in Si or N-Si killed steel materials.

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

第1図はスケール波の概略説明図、第2図はスケールと
地鉄の境界層を示す顕微鏡写真(200倍)、第3図は
加熱炉の概略縦断面図、第4図は酸素濃度とスケール庇
発生率との関係を示すグラフ、第5図は均熱時間とスケ
ール庇発生率との関係を示すグラフ、第6図は在炉時間
とスケール癖発生率との関係を示すグラフである。 1・・・子熱帯、2・・・加熱帯、3・・・均熱帯、4
a〜4p・・・加熱バーナー、5・・・被加熱材、6・
・・煙道、7a〜7c・・・酸素メーター。 ガー図 オ2図 力3図 才4図 ズ5図 矛6図
Figure 1 is a schematic explanatory diagram of scale waves, Figure 2 is a micrograph (200x magnification) showing the boundary layer between scale and steel, Figure 3 is a schematic vertical cross-sectional view of the heating furnace, and Figure 4 is a diagram showing the oxygen concentration and Figure 5 is a graph showing the relationship between the scale eaves occurrence rate, Figure 5 is a graph showing the relationship between the soaking time and the scale eaves generation rate, and Figure 6 is a graph showing the relationship between the furnace time and the scale occurrence rate. . 1... child tropical zone, 2... heating zone, 3... soaking zone, 4
a~4p... Heating burner, 5... Heated material, 6.
... Flue, 7a-7c...Oxygen meter. Gar figure O 2 figure Power 3 figure Sai 4 figure Z 5 figure Spear 6 figure

Claims (1)

【特許請求の範囲】[Claims] 1 C0.05〜0.60%、Mn0.5〜2.0%、
Si0.25〜0.60%、Al0.05%以下、P0
.03%以下、S0.03%以下、残部がFeと不可避
不純物からなるキルド鋼材を加熱炉の均熱帯において、
酸素濃度を2〜8%とし1250℃超〜1320℃未満
の温度領域において10〜80分間均熱したのち、通常
の熱間圧延を行なうことを特徴とするスケール疵のすく
ない熱間圧延鋼材の製造方法。
1 C0.05-0.60%, Mn0.5-2.0%,
Si0.25-0.60%, Al0.05% or less, P0
.. A killed steel material consisting of 0.03% or less, S0.03% or less, and the balance being Fe and unavoidable impurities is heated in a soaking zone of a heating furnace.
Production of hot-rolled steel products with few scale defects, characterized in that normal hot rolling is carried out after soaking for 10-80 minutes at an oxygen concentration of 2-8% in a temperature range of more than 1250°C and less than 1320°C. Method.
JP5488077A 1977-05-13 1977-05-13 Method for manufacturing hot rolled steel materials Expired JPS6015684B2 (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP5488077A JPS6015684B2 (en) 1977-05-13 1977-05-13 Method for manufacturing hot rolled steel materials

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP5488077A JPS6015684B2 (en) 1977-05-13 1977-05-13 Method for manufacturing hot rolled steel materials

Publications (2)

Publication Number Publication Date
JPS53140219A JPS53140219A (en) 1978-12-07
JPS6015684B2 true JPS6015684B2 (en) 1985-04-20

Family

ID=12982890

Family Applications (1)

Application Number Title Priority Date Filing Date
JP5488077A Expired JPS6015684B2 (en) 1977-05-13 1977-05-13 Method for manufacturing hot rolled steel materials

Country Status (1)

Country Link
JP (1) JPS6015684B2 (en)

Cited By (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS62172498A (en) * 1986-01-24 1987-07-29 シャープ株式会社 Alarm system
WO2012081716A1 (en) 2010-12-14 2012-06-21 Jfeスチール株式会社 Nozzle for removing scale of steel plate, scale removing device for steel plate, and method for removing scale of steel plate
WO2012101932A1 (en) 2011-01-26 2012-08-02 Jfeスチール株式会社 Nozzle for descaling steel plate, device for descaling steel plate, and method for descaling steel plate

Families Citing this family (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS62247046A (en) * 1986-04-18 1987-10-28 Nisshin Steel Co Ltd High strength steel for fastening fitting

Cited By (5)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS62172498A (en) * 1986-01-24 1987-07-29 シャープ株式会社 Alarm system
WO2012081716A1 (en) 2010-12-14 2012-06-21 Jfeスチール株式会社 Nozzle for removing scale of steel plate, scale removing device for steel plate, and method for removing scale of steel plate
US9321084B2 (en) 2010-12-14 2016-04-26 Jfe Steel Corporation Descaling nozzle for removing scale from steel sheet, descaling apparatus for removing scale from steel sheet, and descaling method for removing scale from steel sheet
WO2012101932A1 (en) 2011-01-26 2012-08-02 Jfeスチール株式会社 Nozzle for descaling steel plate, device for descaling steel plate, and method for descaling steel plate
US9216446B2 (en) 2011-01-26 2015-12-22 Jfe Steel Corporation Descaling nozzle for removing scale from steel sheet, descaling apparatus for removing scale from steel sheet, and descaling method for removing scale from steel sheet

Also Published As

Publication number Publication date
JPS53140219A (en) 1978-12-07

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