JPS62208B2 - - Google Patents

Info

Publication number
JPS62208B2
JPS62208B2 JP6913083A JP6913083A JPS62208B2 JP S62208 B2 JPS62208 B2 JP S62208B2 JP 6913083 A JP6913083 A JP 6913083A JP 6913083 A JP6913083 A JP 6913083A JP S62208 B2 JPS62208 B2 JP S62208B2
Authority
JP
Japan
Prior art keywords
hours
breakdown
hydrogen
induced cracking
soaking
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
JP6913083A
Other languages
Japanese (ja)
Other versions
JPS59197518A (en
Inventor
Makoto Fukai
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 JP6913083A priority Critical patent/JPS59197518A/en
Publication of JPS59197518A publication Critical patent/JPS59197518A/en
Publication of JPS62208B2 publication Critical patent/JPS62208B2/ja
Granted legal-status Critical Current

Links

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
    • C21D8/00—Modifying the physical properties of ferrous metals or ferrous alloys by deformation combined with, or followed by, heat treatment
    • C21D8/02—Modifying the physical properties of ferrous metals or ferrous alloys by deformation combined with, or followed by, heat treatment during manufacturing of plates or strips

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)

Description

【発明の詳細な説明】 本発明は耐水素誘起割れに優れたラインパイプ
用ホツトコイルの製造方法に関する。 従来耐水素誘起割れ性を必要とするサワーガス
用ホツトコイルの製造方法としては、極低硫化
(S≦0.002)、Cu、Ni添加、Ca添加などの処
理を施し、通常のプロセスすなわち連鋳スラブを
加熱炉で加熱し、熱間連続圧延により製造してい
た。 しかし、最近はH2Sガスを多く含む原油を採油
するようになつたため、さらに耐サワー性の優れ
たラインパイプを要求されるようになつた。 耐水素誘起割れ試験は、従来はPH=5.2程度で
行われていたが最近ではPH=3.5〜3.8での試験を
要求されている。 PH=3.5〜3.8では、従来の製造方法によるコイ
ルでは水素誘起割れが発生し、要求を満足できな
い。 この原因として連鋳スラブの中心偏析に起因す
るホツトコイル板厚中心部の硬化層が割れ起点に
なつていることが考えられる。 本発明は連鋳スラブの中心偏析を拡散させ耐水
素誘起割れ性を向上させることを目的とするもの
で、連鋳スラブをブレークダウン圧延し、次いで
スラブ加熱を行つた後熱間連続圧延してコイルを
製造することにより好結果を得、この知見により
完成されたもので、PH=3.5〜3.8の試験でも水素
誘起割れのない優れたサワーガス用ラインパイプ
コイルを製造するものである。 本発明は C≦0.15wt% Si=0.05〜0.50wt% Mn=0.50〜1.50wt% P≦0.020wt% S≦0.003wt% Al≦0.070wt% Cu=0.10〜0.50wt% Ni=0.10〜0.50wt% Ca=0.0010〜0.0060wt% 残部Feおよび不可避的不純物 から成る連鋳スラブを、加熱条件1250℃〜1350℃
で5時間〜10時間保持した後、ブレークダウン率
20%〜40%でブレークダウン圧延し、次いで加熱
条件1150℃〜1300℃で3時間〜5時間保持した
後、熱間連続圧延を行うことを特徴とする耐水素
誘起割れに優れたラインパイプ用ホツトコイルの
製造方法である。 本発明の適用されるホツトコイルは厚さ3.5〜
25mmである。厚さ3.5mmはラインパイプ材の実用
上の下限であり、厚さ25mmはホツトコイルとして
現在製造可能な上限である。 連鋳スラブのブレークダウン圧延は、加熱炉内
での中心偏析の軽減を目的としたものでブレーク
ダウン時の均熱温度、保持時間、ブレークダウン
率等の条件が水素誘起割れに対して重要な要因で
ある。ここにブレークダウン率とは、 (連鋳スラブ厚−ブレークダウン後スラブ厚) ÷(連鋳スラブ厚)×100(%) である。 第1図に上記条件の対サワー特性に対する影響
を示す。熱間連続圧延前の加熱時間は各条件とも
3時間で、一定である。 第1図の結果を要約すると次のようになる。 (1) ブレークダウン率10%の場合、均熱時間を10
時間以上にすれば耐サワー特性は良好になる
が、割れを零にすることはできない。 (2) ブレークダウン率20%、30%の場合、均熱温
度を1250℃〜1300℃にすれば、均熱時間5時間
以上で割れが零とある。 (3) ブレークダウン率20%、30%の場合、均熱温
度1200℃でも15時間以上保持すれば割れが零に
なる。 加熱炉内での均熱により、スラブ中心部のC、
P、Mnなどが拡散する。拡散を促進するために
は、均熱時間を長くし、均熱温度を高くすればよ
いが、スラブ中心部のポロシテイーを圧着した方
が、拡散はより促進される。従つて、連鋳スラブ
のブレークダウン率20%以上を確保するブレーク
ダウン圧延により、加熱炉内での中心偏析の軽減
は顕著となる。しかし、歩止り、および実操業上
からブレークダウン率の上限は40%とする。 また、ブレークダウン圧延前のスラブ均熱も
C、P、Mnなどの拡散を促進する。第1図から
明らかなように1250℃以上で均熱すれば5時間で
十分な効果がある。1200℃の場合は15時間以上均
熱すれば効果が出るが、長時間均熱するとスケー
ルの発生が多くなり、スケール疵発生の懸念があ
る。 スケール疵および実操業上の問題から温度は
1350℃、時間は10時間を上限とする。 一方、熱間連続圧延前の加熱条件の影響は第2
図に示す通りである。加熱時間3時間以上であれ
ば、耐サワー性は十分である。加熱温度は機械的
性質の問題から規制され、また操業上の問題から
在炉時間が規制される。工業ベースを考慮すれ
ば、在炉時間は3〜4時間が適当である。 化学成分の規制理由については、次の通りであ
る。 C:0.15wt%以上では靭性、溶接性の問題点が
ある。 Si:脱酸剤としてて添加するが、0.50wt%を越
えるとでは脆性が増加できる。 Mn:0.50wt%未満では、強度を得ることがで
きない。1.50wt%を越えると脆性が大とな
る。 P:水素誘起割れに大きな要因となる元素であ
り、低いほど有利であるが、工業製造上から
0.020wt%未満とする。 S:0.003wt%未満に押えることが必須の条件
であり、低いほど水素誘起割れに対して有利
である。 Al:Siと同様に脱酸剤として添加する。
0.070wt%以上では鋼質が劣化する。 Cu:水素誘起割れに対して有効な元素である
が、0.10wt%未満では効果がなく、0.50wt%
を越えると溶接性が劣化する。 Ni:Cu脆化防止のためCuと等量添加する。 Ca:硫化物の形態制御を行い、水素誘起割れ
に対し有効である。ただし、Ca/S≧2.0に
なるように添加することが必要であり、上限
は、0.0060wt%を越えると、CaOが多くな
り、清浄度が劣化する。 その他:材質要求よりNb、V、Tiなどを添加
する。 次に本発明の実施例を第1表にまとめて示す。 実施例1〜5はMnレベルが1.10wt%、実施例
6〜9はMnレベルが0.60wt%のラインパイプ用
の厚さ15.88mmのコイルで、各化学成分は次の通
りである。 実施例 1〜5 C:0.07wt%、 Si:0.24wt%、 Mn:1.12wt%、 P:0.013wt%、 S:0.0008wt%、 Al:0.037wt%、 Nb:0.0031wt%、 V:− Ca:0.0036wt% 実施例 6〜9 C:0.07wt%、 Si:0.16wt%、 Mn:0.62wt%、 P:0.016、 S:0.0009wt%、 Al:0.045wt%、 Nb:0.011wt%、 V:− Ca:0.0033wt% 第1表からサイジング条件を加熱温度1250℃、
保持時間5時間以上、ブレークダウン率20%以上
としてブレークダウン圧延し、次いで加熱時間を
3時間とすれば、PH=3.5における耐サワー性は
良好な成績を示し、本発明の優れた効果が明らか
である。 【表】
DETAILED DESCRIPTION OF THE INVENTION The present invention relates to a method for manufacturing a hot coil for a line pipe that has excellent resistance to hydrogen-induced cracking. Conventionally, the manufacturing method for hot coils for sour gas, which requires hydrogen-induced cracking resistance, involves applying treatments such as ultra-low sulfidation (S≦0.002), adding Cu, Ni, and Ca, and then heating the continuous cast slab using the normal process. It was heated in a furnace and manufactured by continuous hot rolling. However, recently, as crude oil containing a large amount of H 2 S gas has been extracted, there has been a demand for line pipes with even better sour resistance. Hydrogen-induced cracking tests were previously conducted at a pH of about 5.2, but recently tests at a pH of 3.5 to 3.8 are required. When pH=3.5 to 3.8, hydrogen-induced cracking occurs in coils manufactured using conventional methods, and the requirements cannot be met. The reason for this is thought to be that the hardened layer at the center of the thickness of the hot coil plate, which is caused by center segregation of the continuous cast slab, becomes the starting point for cracks. The purpose of the present invention is to improve hydrogen-induced cracking resistance by diffusing the center segregation of a continuously cast slab. Good results were obtained by manufacturing the coil, and this knowledge was completed to manufacture an excellent line pipe coil for sour gas without hydrogen-induced cracking even in tests of PH = 3.5 to 3.8. The present invention is as follows: C≦0.15wt% Si=0.05-0.50wt% Mn=0.50-1.50wt% P≦0.020wt% S≦0.003wt% Al≦0.070wt% Cu=0.10-0.50wt% Ni=0.10-0.50wt % Ca = 0.0010~0.0060wt% A continuously cast slab consisting of the balance Fe and unavoidable impurities was heated at 1250℃~1350℃.
After holding for 5 to 10 hours, the breakdown rate
For line pipes with excellent resistance to hydrogen-induced cracking, characterized by performing breakdown rolling at 20% to 40%, then holding at heating conditions of 1150°C to 1300°C for 3 to 5 hours, and then performing continuous hot rolling. This is a method of manufacturing a hot coil. The hot coil to which the present invention is applied has a thickness of 3.5~
It is 25mm. A thickness of 3.5 mm is the practical lower limit for line pipe material, and a thickness of 25 mm is the upper limit that can currently be manufactured as a hot coil. Breakdown rolling of continuous cast slabs is aimed at reducing center segregation in the heating furnace, and conditions such as soaking temperature, holding time, and breakdown rate during breakdown are important for hydrogen-induced cracking. It is a factor. Here, the breakdown rate is (continuously cast slab thickness - slab thickness after breakdown) ÷ (continuously cast slab thickness) x 100 (%). FIG. 1 shows the influence of the above conditions on the sour characteristics. The heating time before continuous hot rolling was constant at 3 hours under each condition. The results shown in Figure 1 can be summarized as follows. (1) If breakdown rate is 10%, soaking time is 10
If the time is exceeded, sour resistance properties will improve, but cracking cannot be reduced to zero. (2) When the breakdown rate is 20% or 30%, if the soaking temperature is 1250°C to 1300°C, there will be no cracking after soaking for 5 hours or more. (3) When the breakdown rate is 20% or 30%, even if the soaking temperature is 1200℃, there will be no cracking if the product is held for 15 hours or more. By soaking in the heating furnace, C in the center of the slab,
P, Mn, etc. diffuse. In order to promote diffusion, it is possible to lengthen the soaking time and increase the soaking temperature, but diffusion is further promoted by compressing the porosities at the center of the slab. Therefore, breakdown rolling that ensures a breakdown rate of 20% or more in the continuously cast slab significantly reduces center segregation in the heating furnace. However, from the viewpoint of yield and actual operation, the upper limit of the breakdown rate is set at 40%. In addition, soaking the slab before breakdown rolling also promotes the diffusion of C, P, Mn, etc. As is clear from Figure 1, if soaked at 1250°C or higher, 5 hours will be sufficient. In the case of 1200℃, soaking for 15 hours or more will be effective, but soaking for a long time will increase the formation of scale, and there is a concern that scale defects may occur. Due to scale flaws and operational issues, the temperature is
1350℃, maximum time is 10 hours. On the other hand, the influence of heating conditions before continuous hot rolling is second to none.
As shown in the figure. If the heating time is 3 hours or more, the sour resistance is sufficient. The heating temperature is regulated due to mechanical property issues, and the furnace time is regulated due to operational issues. Considering the industrial basis, the appropriate furnace time is 3 to 4 hours. The reasons for regulating chemical components are as follows. C: If it exceeds 0.15wt%, there will be problems with toughness and weldability. Si: Added as a deoxidizing agent, but if it exceeds 0.50wt%, brittleness may increase. Mn: If it is less than 0.50wt%, strength cannot be obtained. If it exceeds 1.50wt%, brittleness becomes large. P: This is an element that is a major factor in hydrogen-induced cracking, and the lower the value, the more advantageous it is, but from the viewpoint of industrial manufacturing
Less than 0.020wt%. It is an essential condition to suppress S: to less than 0.003 wt%, and the lower the S content, the more advantageous it is to hydrogen-induced cracking. Al: Added as a deoxidizing agent like Si.
If it exceeds 0.070wt%, the steel quality will deteriorate. Cu: An effective element against hydrogen-induced cracking, but it is ineffective at less than 0.10wt%, and 0.50wt%
If it exceeds this, weldability will deteriorate. Ni: Added in the same amount as Cu to prevent Cu embrittlement. Ca: Controls the morphology of sulfides and is effective against hydrogen-induced cracking. However, it is necessary to add so that Ca/S≧2.0, and if the upper limit exceeds 0.0060 wt%, CaO will increase and the cleanliness will deteriorate. Others: Nb, V, Ti, etc. are added according to material requirements. Next, Examples of the present invention are summarized in Table 1. Examples 1 to 5 are 15.88 mm thick coils for line pipes with a Mn level of 1.10 wt%, and Examples 6 to 9 have a Mn level of 0.60 wt%, and the chemical components are as follows. Examples 1 to 5 C: 0.07wt%, Si: 0.24wt%, Mn: 1.12wt%, P: 0.013wt%, S: 0.0008wt%, Al: 0.037wt%, Nb: 0.0031wt%, V: - Ca: 0.0036wt% Examples 6 to 9 C: 0.07wt%, Si: 0.16wt%, Mn: 0.62wt%, P: 0.016, S: 0.0009wt%, Al: 0.045wt%, Nb: 0.011wt%, V: - Ca: 0.0033wt% From Table 1, the sizing conditions are heating temperature 1250℃,
When breakdown rolling was performed with a holding time of 5 hours or more and a breakdown rate of 20% or more, and then a heating time of 3 hours, the sour resistance at PH = 3.5 showed good results, clearly demonstrating the excellent effects of the present invention. It is. 【table】

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

第1図は連鋳スラブのブレークダウン条件と耐
サワー特性を示すグラフ、第2図は熱間連続圧延
前の均熱時間と耐サワー特性を示すグラフであ
る。
FIG. 1 is a graph showing breakdown conditions and sour resistance characteristics of a continuously cast slab, and FIG. 2 is a graph showing soaking time before continuous hot rolling and sour resistance characteristics.

Claims (1)

【特許請求の範囲】 1 C≦0.15wt% Si=0.05〜0.50wt% Mn=0.05〜1.50wt% P≦0.020wt% S≦0.003wt% Al≦0.070wt% Cu=0.10〜0.50wt% Ni=0.10〜0.50wt% Ca=0.0010〜0.0060wt% 残部Feおよび不可避的不純物 から成る連鋳スラブを、加熱条件1250℃〜1350℃
で5時間〜10時間保持した後、ブレークダウン率
20%〜40%でブレークダウン圧延し、次いで加熱
条件1150℃〜1300℃で3時間〜5時間保持した
後、熱間連続圧延を行うことを特徴とする耐水素
誘起割れに優れたラインパイプ用ホツトコイルの
製造方法。
[Claims] 1 C≦0.15wt% Si=0.05-0.50wt% Mn=0.05-1.50wt% P≦0.020wt% S≦0.003wt% Al≦0.070wt% Cu=0.10-0.50wt% Ni= A continuous cast slab consisting of 0.10 to 0.50wt% Ca = 0.0010 to 0.0060wt% with the balance Fe and unavoidable impurities was heated at 1250℃ to 1350℃.
After holding for 5 to 10 hours, the breakdown rate
For line pipes with excellent resistance to hydrogen-induced cracking, characterized by performing breakdown rolling at 20% to 40%, then holding at heating conditions of 1150°C to 1300°C for 3 to 5 hours, and then performing continuous hot rolling. Method of manufacturing hot coils.
JP6913083A 1983-04-21 1983-04-21 Manufacture of hot coil for line pipe efficient in hydrogen induced crack resistance Granted JPS59197518A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP6913083A JPS59197518A (en) 1983-04-21 1983-04-21 Manufacture of hot coil for line pipe efficient in hydrogen induced crack resistance

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP6913083A JPS59197518A (en) 1983-04-21 1983-04-21 Manufacture of hot coil for line pipe efficient in hydrogen induced crack resistance

Publications (2)

Publication Number Publication Date
JPS59197518A JPS59197518A (en) 1984-11-09
JPS62208B2 true JPS62208B2 (en) 1987-01-06

Family

ID=13393748

Family Applications (1)

Application Number Title Priority Date Filing Date
JP6913083A Granted JPS59197518A (en) 1983-04-21 1983-04-21 Manufacture of hot coil for line pipe efficient in hydrogen induced crack resistance

Country Status (1)

Country Link
JP (1) JPS59197518A (en)

Families Citing this family (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS61221326A (en) * 1985-03-27 1986-10-01 Nippon Kokan Kk <Nkk> Production of steel material having excellent resistance to sulfide corrosion cracking
JPH04143217A (en) * 1990-10-05 1992-05-18 Kobe Steel Ltd Production of normalized type steel plate excellent in hydrogen induced cracking resistance
KR100723166B1 (en) 2005-12-24 2007-05-30 주식회사 포스코 Line pipe steel with excellent toughness, high strength and resistance to hydrogen organic cracking and its manufacturing method

Also Published As

Publication number Publication date
JPS59197518A (en) 1984-11-09

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