JPH0241400B2 - - Google Patents
Info
- Publication number
- JPH0241400B2 JPH0241400B2 JP20151281A JP20151281A JPH0241400B2 JP H0241400 B2 JPH0241400 B2 JP H0241400B2 JP 20151281 A JP20151281 A JP 20151281A JP 20151281 A JP20151281 A JP 20151281A JP H0241400 B2 JPH0241400 B2 JP H0241400B2
- Authority
- JP
- Japan
- Prior art keywords
- rolling
- steel
- rate
- carbon
- 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
Links
- 238000005096 rolling process Methods 0.000 claims description 40
- 229910000975 Carbon steel Inorganic materials 0.000 claims description 25
- 229910000831 Steel Inorganic materials 0.000 claims description 25
- 239000010959 steel Substances 0.000 claims description 25
- 239000010962 carbon steel Substances 0.000 claims description 24
- 229910052799 carbon Inorganic materials 0.000 claims description 21
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 claims description 20
- 238000000034 method Methods 0.000 claims description 12
- 238000005260 corrosion Methods 0.000 claims description 10
- 238000004519 manufacturing process Methods 0.000 claims description 10
- 229910000963 austenitic stainless steel Inorganic materials 0.000 claims description 9
- 230000001186 cumulative effect Effects 0.000 claims description 9
- 229910001220 stainless steel Inorganic materials 0.000 description 23
- 239000000463 material Substances 0.000 description 20
- 239000010935 stainless steel Substances 0.000 description 20
- 230000007797 corrosion Effects 0.000 description 9
- 238000001556 precipitation Methods 0.000 description 9
- UFGZSIPAQKLCGR-UHFFFAOYSA-N chromium carbide Chemical compound [Cr]#C[Cr]C#[Cr] UFGZSIPAQKLCGR-UHFFFAOYSA-N 0.000 description 8
- 229910003470 tongbaite Inorganic materials 0.000 description 8
- 238000010438 heat treatment Methods 0.000 description 6
- 239000002131 composite material Substances 0.000 description 5
- XEEYBQQBJWHFJM-UHFFFAOYSA-N Iron Chemical compound [Fe] XEEYBQQBJWHFJM-UHFFFAOYSA-N 0.000 description 4
- 230000007423 decrease Effects 0.000 description 4
- 239000011651 chromium Substances 0.000 description 3
- 239000000203 mixture Substances 0.000 description 3
- RWSOTUBLDIXVET-UHFFFAOYSA-N Dihydrogen sulfide Chemical compound S RWSOTUBLDIXVET-UHFFFAOYSA-N 0.000 description 2
- 229910052804 chromium Inorganic materials 0.000 description 2
- -1 chromium carbides Chemical class 0.000 description 2
- 238000005253 cladding Methods 0.000 description 2
- 230000000694 effects Effects 0.000 description 2
- 239000012467 final product Substances 0.000 description 2
- 239000012535 impurity Substances 0.000 description 2
- 229910052742 iron Inorganic materials 0.000 description 2
- 229910052748 manganese Inorganic materials 0.000 description 2
- 238000003466 welding Methods 0.000 description 2
- 102100032884 Neutral amino acid transporter A Human genes 0.000 description 1
- 101710160582 Neutral amino acid transporter A Proteins 0.000 description 1
- 206010070834 Sensitisation Diseases 0.000 description 1
- 239000000853 adhesive Substances 0.000 description 1
- 230000001070 adhesive effect Effects 0.000 description 1
- 229910001566 austenite Inorganic materials 0.000 description 1
- 230000006399 behavior Effects 0.000 description 1
- 229910052802 copper Inorganic materials 0.000 description 1
- 230000003247 decreasing effect Effects 0.000 description 1
- 230000012447 hatching Effects 0.000 description 1
- 238000005098 hot rolling Methods 0.000 description 1
- 238000005304 joining Methods 0.000 description 1
- 239000002648 laminated material Substances 0.000 description 1
- 230000013011 mating Effects 0.000 description 1
- 229910052750 molybdenum Inorganic materials 0.000 description 1
- 229910052759 nickel Inorganic materials 0.000 description 1
- 229910052758 niobium Inorganic materials 0.000 description 1
- 230000001590 oxidative effect Effects 0.000 description 1
- 238000006116 polymerization reaction Methods 0.000 description 1
- 239000002244 precipitate Substances 0.000 description 1
- 239000000047 product Substances 0.000 description 1
- 230000008313 sensitization Effects 0.000 description 1
- 238000000926 separation method Methods 0.000 description 1
- 238000010583 slow cooling Methods 0.000 description 1
- 229910052715 tantalum Inorganic materials 0.000 description 1
- 238000005496 tempering Methods 0.000 description 1
- 229910052720 vanadium Inorganic materials 0.000 description 1
- 229910052726 zirconium Inorganic materials 0.000 description 1
Classifications
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B23—MACHINE TOOLS; METAL-WORKING NOT OTHERWISE PROVIDED FOR
- B23K—SOLDERING OR UNSOLDERING; WELDING; CLADDING OR PLATING BY SOLDERING OR WELDING; CUTTING BY APPLYING HEAT LOCALLY, e.g. FLAME CUTTING; WORKING BY LASER BEAM
- B23K20/00—Non-electric welding by applying impact or other pressure, with or without the application of heat, e.g. cladding or plating
- B23K20/04—Non-electric welding by applying impact or other pressure, with or without the application of heat, e.g. cladding or plating by means of a rolling mill
Landscapes
- Engineering & Computer Science (AREA)
- Mechanical Engineering (AREA)
- Pressure Welding/Diffusion-Bonding (AREA)
Description
本発明は高靭性高耐食性クラツド鋼板の製造方
法の創案に係り、サワーなどの環境下で使用され
るラインパイプ材等に要求される高耐食性をステ
ンレスによつて得しめると共に高靭性且つ高せん
断強度の特質を具備した非調質ステンレスクラツ
ド鋼板を適切に製造することのできる方法を得よ
うとするものである。
鋼板の使用条件が苛酷になるに従い高耐食性の
観点よりして近年クラツド鋼板の使用が増加して
いるが、この場合において単に耐食性のみでなく
高靭性も要求されることが多い。例えばサワーガ
スなどの環境下で使用されるラインパイプ材等に
おいてはこのような高耐食性高靭性が共に強く要
求される。然して圧延クラツド鋼板の製造におい
ては良好な接合性を得るために高温高圧下の圧延
を行うのが通常であり、圧延温度、パススケジユ
ール、パス圧下率などの圧延条件は主として接合
性の観点によつてのみ決定されている。従つて母
材が厳しい低温靭性や高い延性が要求されるよう
な場合にはクラツド圧延の後に、熱処理が施され
るのが通常である。ところがこのように熱処理を
施すことは生産コストの上昇及び生産能率の低下
を招く不利がある。又その合わせ材がオーステナ
イト系ステンレス鋼の場合においてσ相脆化、鋭
敏化(徐冷によるCr炭化物の析出に伴う脆化)
等の各種脆化現象があるため充分な時間の焼もど
し処理が行えないなど熱処理方法に大きな制約が
あり、充分な低温靭性や高いせん断強さを得るに
は大きな困難が伴うことになる。
本発明は上記したような実情に鑑み検討を重ね
て創案されたもので、炭素鋼とオーステナイトス
テンレス鋼による部材を重ね合せて圧延しクラツ
ド鋼板を製造するに当つて、前記炭素鋼の炭素含
有量を0.12%以下とすると共にオーステナイトス
テンレス鋼の炭素含有量を0.05%以下となし、し
かも1000〜1250℃の温度域においては下記する
式の関係を満す接合粗圧下率による圧延を行い、
又650〜950℃の温度域においては下記式の関係
を満す累積圧下率による圧延を行うことを特徴と
する高靭性高耐食性クラツド鋼板の製造方法であ
る。
累積粗圧下率(%)≧15%+0.2×〔CR率(%)〕…
20%≦CR率≦〔90%−200×{炭素鋼の含有炭素量(w
t%)}〕…
但し上記、式においてCR率は650〜950℃
の温度域における累積圧下率を示すものである。
このような本発明について更に説明すると、圧
延ままで高靭性鋼板を製造する方法として制御圧
延法が知られているが、上記したようなオーステ
ナイト系ステンレスクラツド鋼板の製造にこの制
御圧延法を用いると、圧延過程(950〜650℃)で
クロム炭化物の析出が顕著に顕われ、ステンレス
鋼自身の耐食性を低下し、又炭素鋼とステンレス
鋼界面の接合力低下を来すのでステンレスクラツ
ド鋼板の容易に該制御圧延技術を採用することは
困難と考えられる。ところが本発明者等は圧延パ
ターンの詳細な検討を行つた結果、制御圧延され
たステンレスクラツド鋼板におけるクロム炭化物
の析出を抑制し、炭素鋼−ステンレス鋼界面での
充分なせん断強度(例えばJISで規定される20
Kg/mm2以上)を得るための因子として、
炭素鋼のC量
オーステナイト系ステンレス鋼のC量
1250〜1000℃間の全圧下率
950℃以下の温度域での全圧下率
の如きを制御することによりこのせん断強度を適
切に確保されることを見出した。即ち本発明にお
いては熱間圧延の際に特殊なパススケジユールを
採用することにより高靭性非調質のステンレスク
ラツド鋼を得るものである。
上記したような本発明によるものの技術的内容
について更に説明すると、圧延クラツド鋼板など
の製造において、C0.12%の炭素鋼鋼片とC
0.05%のオーステナイト系スンレス鋼片を組み合
わせ、1250℃未満、650℃以上の温度範囲で圧延
するに当つて、
1250℃以下、1000℃以上の温度間の接合粗圧
下率を次の式で示す下限圧下率以上で圧延を
行う。
接合粗圧下率(%)≧15%+0.2×〔950℃以下の累積圧
下率(%)〕……
又上記に続いて950℃以下の温度域での累
積圧下率(CR率)が次の式で示される範囲
の圧延を行う。
20%≦CR率(%)≦〔90%−200×{炭素鋼のC量;wt
%}〕…
のような圧延パターンを彩用する。即ちこの
によつて示される圧延条件は第1図においてハツ
チングを以て示す通りであつて、このような圧延
パターンにより制御圧延過程におけるクロム炭化
物の析出を制御し、炭素鋼−ステンレス鋼界面で
20Kg/mm2以上の高せん断強度を得ることができ
る。なお上記のような圧延に先行して行われる鋼
片の加熱については特に限定する必要がないが、
その温度を1050〜1300℃とすることが好ましい。
然して上記のように接合粗圧下率を規定した
理由について説明すると、炭素鋼とステンレス鋼
との界面において高せん断強度を得るには、前記
のような高温域で一定以上の大圧下を加えること
が基本的に重要であることは明らかであるが、低
温域で制御圧延を行う場合にはそのCR率の大き
さに応じてこの高温域における接合粗圧下率を増
大させることが必要である。つまり低温域での制
御圧延は前記界面近傍に累積的に変形歪を与え、
せん断強度を漸次低下させるからである。
又前記のようにCR率の上限を規定する理由
は、高CR率条件では、クロム炭化物析出が顕著
な低温域(950〜650℃)における鋼材滞在時間が
長くなるとともに界面近傍の変形歪の増大するこ
とによつてクロム炭化物析出が促進される。即ち
本発明者等が検討した結果によると式に示した
上限以上のCR率ではせん断強さを20Kg/mm2以上
に保持することが不可能である。又この上限CR
率は母材の炭素含有量に依存し、上記の圧延で
上限CR率を超えた圧延を行うと炭素鋼とステン
レス鋼の界面にクロム炭化物の析出を生じ、せん
断強さの著しい低下を生ずる。理論的には上記
CR率は母材炭素鋼およびステンレス鋼合わせ材
双方の炭素量に依存すると考えられるが、通常は
母材炭素鋼の炭素量の方が数倍高く、上限CR率
は実質的にこの母材炭素量に支配される。
又上記においてCR率の下限を規定した理由
は、これ以下のCR率では炭素鋼の靭性水準を充
分に高く(例えばDWTT試験における85%
SATT≦0℃)することが不可能である。
更に母材炭素鋼とステンレス合わせ材の上限炭
素量を規定した理由については、母材炭素量が
0.12%を超える領域ではクロム炭化物の析出が急
激に増大し、前記における式が成立しなくな
つて、本発明に従つて圧延を行つても充分な接合
強度を得ることが不可能である。
又ステンレス合わせ材の炭素量が0.052%を超
えると、制御圧延されたステンレス鋼表面の耐食
性が低下する。更に圧延温度が650℃未満となる
と両鋼片、特に炭素鋼の変形抵抗が著しく増大し
て圧延が非常に困難となると共に両鋼片間の接着
強度が低下してくる。又圧延温度を1250℃以上と
するとオーステナイト粒が粗大化して本発明で目
的とする高靭性クラツド鋼板が得られない。従つ
て圧延温度は650〜1250℃とする必要がある。
なお圧延に当つては炭素鋼−ステンレス鋼−ス
テンレス鋼−炭素鋼のように重合し、そのステン
レス鋼間には圧延後にオーステナイトステンレス
鋼同志の間の分離を容易ならしめるセパレータを
介在させると共に上下の炭素鋼板寸法を中間のス
テンレス鋼板より大とし、更に圧延に先立つて行
われる加熱中にステンレス−炭素鋼の接合面が酸
化するのを防止するため上下の炭素鋼板四周を溶
接したサンドイツチ状体を準備し、このものを加
熱圧延するものである。
本発明によるものの具体的な実施例について説
明すると以下の通りである。
本発明者等の具体的に採用した供試鋼の組成は
次の第1表に示す通りであり、母材と合わせ材は
何れも表面をシヨツトブラストして用いた。なお
合わせ材厚さは3mmであり、上記したようなサン
ドイツチ法に従つて準備したものを採用した。
The present invention relates to the creation of a method for manufacturing a clad steel plate with high toughness and high corrosion resistance, and which uses stainless steel to achieve the high corrosion resistance required for line pipe materials used in environments such as sour weather, as well as high toughness and high shear strength. The object of the present invention is to obtain a method that can appropriately manufacture a non-tempered stainless steel clad steel sheet having the following characteristics. As the conditions under which steel plates are used have become more severe, the use of clad steel plates has increased in recent years from the viewpoint of high corrosion resistance, but in this case, not only corrosion resistance but also high toughness is often required. For example, line pipe materials used in environments such as sour gas are strongly required to have both such high corrosion resistance and high toughness. However, in the production of rolled clad steel sheets, it is common to perform rolling at high temperatures and pressures in order to obtain good bondability, and rolling conditions such as rolling temperature, pass schedule, and pass reduction ratio are mainly determined from the viewpoint of bondability. Only the number of points has been determined. Therefore, when the base material is required to have severe low-temperature toughness or high ductility, heat treatment is usually performed after clad rolling. However, such heat treatment has the disadvantage of increasing production costs and decreasing production efficiency. In addition, when the composite material is austenitic stainless steel, σ phase embrittlement and sensitization (embrittlement due to precipitation of Cr carbide due to slow cooling) occur.
Due to various embrittlement phenomena such as embrittlement phenomena, there are major restrictions on heat treatment methods, such as the inability to perform tempering treatment for a sufficient period of time, and it is difficult to obtain sufficient low-temperature toughness and high shear strength. The present invention was devised after repeated studies in view of the above-mentioned circumstances, and in producing a clad steel plate by stacking and rolling members made of carbon steel and austenitic stainless steel, the carbon content of the carbon steel is 0.12% or less, and the carbon content of the austenitic stainless steel is 0.05% or less, and in the temperature range of 1000 to 1250°C, rolling is performed at a welding rough reduction rate that satisfies the relationship of the following formula,
Further, the method for producing a high toughness and high corrosion resistance clad steel sheet is characterized in that rolling is carried out at a cumulative reduction rate that satisfies the relationship of the following formula in the temperature range of 650 to 950°C. Cumulative rough reduction rate (%) ≧ 15% + 0.2 × [CR rate (%)]...
20% ≦ CR rate ≦ [90% − 200 × {carbon content of carbon steel (w
t%)}]... However, in the above formula, the CR rate is 650 to 950℃
This shows the cumulative rolling reduction rate in the temperature range. To further explain the present invention, a controlled rolling method is known as a method for manufacturing high-toughness steel sheets as rolled, and this controlled rolling method is used to manufacture the above-mentioned austenitic stainless steel clad steel sheets. During the rolling process (950 to 650°C), chromium carbide precipitation becomes noticeable, reducing the corrosion resistance of the stainless steel itself, and reducing the bonding strength between the carbon steel and stainless steel interface. It is considered difficult to easily adopt this controlled rolling technology. However, as a result of a detailed study of the rolling pattern, the inventors of the present invention have succeeded in suppressing the precipitation of chromium carbide in controlled rolled stainless steel clad steel sheets and achieving sufficient shear strength at the carbon steel-stainless steel interface (for example, according to JIS standards). 20 specified
Kg/mm 2 or more), the following factors are controlled: C content in carbon steel, C content in austenitic stainless steel, Total reduction rate between 1250 and 1000℃, and Total reduction rate in the temperature range below 950℃. It has been found that this shear strength can be appropriately secured by doing this. That is, in the present invention, a high-toughness, non-heat-refined stainless clad steel is obtained by employing a special pass schedule during hot rolling. To further explain the technical content of the invention as described above, in the production of rolled clad steel sheets, etc., carbon steel billets containing 0.12% C and carbon
When combining 0.05% austenitic stainless steel slabs and rolling them at a temperature range of less than 1250°C and more than 650°C, the lower limit of the joint crude reduction rate between temperatures of less than 1250°C and more than 1000°C is determined by the following formula. Rolling is performed at a reduction rate or higher. Crude joint reduction rate (%) ≧ 15% + 0.2 × [cumulative reduction rate (%) below 950℃]... Also, following the above, the cumulative reduction rate (CR rate) in the temperature range below 950℃ is as follows: Rolling is performed within the range shown by the formula. 20% ≦ CR rate (%) ≦ [90% - 200 × {C content of carbon steel; wt
%}]... Use a rolling pattern like this. In other words, the rolling conditions indicated by this are as shown by hatching in Fig. 1, and this rolling pattern controls the precipitation of chromium carbide in the controlled rolling process and improves the stability at the carbon steel-stainless steel interface.
High shear strength of 20Kg/mm2 or more can be obtained. It should be noted that there is no need to particularly limit the heating of the steel billet that is carried out prior to rolling as described above.
Preferably, the temperature is 1050-1300°C. However, to explain the reason for specifying the crude joining reduction rate as mentioned above, in order to obtain high shear strength at the interface between carbon steel and stainless steel, it is necessary to apply a large reduction above a certain level in the high temperature range as mentioned above. Although it is clear that it is fundamentally important, when performing controlled rolling in a low temperature range, it is necessary to increase the joint rough reduction rate in this high temperature range in accordance with the magnitude of the CR ratio. In other words, controlled rolling in a low temperature region cumulatively gives deformation strain near the interface,
This is because the shear strength is gradually reduced. The reason for specifying the upper limit of the CR rate as mentioned above is that under high CR rate conditions, the residence time of steel in the low temperature range (950 to 650°C) where chromium carbide precipitation is noticeable increases, and the deformation strain near the interface increases. By doing so, chromium carbide precipitation is promoted. That is, according to the results of studies conducted by the present inventors, it is impossible to maintain the shear strength at 20 Kg/mm 2 or more with a CR rate greater than the upper limit shown in the formula. Also, this upper limit CR
The CR rate depends on the carbon content of the base material, and if the above-mentioned rolling is performed above the upper limit CR rate, chromium carbide will precipitate at the interface between carbon steel and stainless steel, resulting in a significant decrease in shear strength. Theoretically the above
It is thought that the CR rate depends on the carbon content of both the base material carbon steel and the stainless steel composite material, but the carbon content of the base material carbon steel is usually several times higher, and the upper limit CR rate is essentially this base material carbon content. ruled by quantity. Also, the reason for specifying the lower limit of the CR rate above is that a CR rate below this is sufficient to maintain the toughness level of carbon steel (for example, 85% in the DWTT test).
SATT≦0℃) is not possible. Furthermore, the reason for specifying the upper limit carbon content for base material carbon steel and stainless steel composite material is that the base material carbon content is
In a region exceeding 0.12%, the precipitation of chromium carbides increases rapidly, and the above equation no longer holds true, making it impossible to obtain sufficient joint strength even if rolling is performed according to the present invention. If the carbon content of the stainless steel composite material exceeds 0.052%, the corrosion resistance of the controlled rolled stainless steel surface will decrease. Further, when the rolling temperature is lower than 650°C, the deformation resistance of both pieces of steel, especially carbon steel, increases significantly, making rolling extremely difficult, and the adhesive strength between the pieces of steel decreases. Furthermore, if the rolling temperature is 1250° C. or higher, the austenite grains will become coarse, making it impossible to obtain the high toughness clad steel sheet targeted by the present invention. Therefore, the rolling temperature needs to be 650 to 1250°C. During rolling, the polymerization occurs as carbon steel - stainless steel - stainless steel - carbon steel, and a separator is interposed between the stainless steels to facilitate separation between the austenitic stainless steels after rolling. The carbon steel plate size is larger than the intermediate stainless steel plate, and in order to prevent the stainless steel-carbon steel joint surface from oxidizing during heating prior to rolling, a sandwich-shaped body is prepared by welding the four circumferences of the upper and lower carbon steel plates. This material is then heated and rolled. Specific embodiments according to the present invention will be described below. The composition of the test steel specifically adopted by the present inventors is shown in Table 1 below, and both the base material and the mating material were used with their surfaces shot blasted. The thickness of the laminated material was 3 mm, and it was prepared according to the Sanderuch method as described above.
【表】
加熱温度は1250℃であり、次いで第2表に示す
ような母材と合わせ材の各種組合わせにより元厚
のものを同じく第2表に示すような圧延条件で圧
延したものについての機械的性質をこの第2表に
おいて併せて示す。なお何れのパススケジユール
においても仕上温度は700℃で、仕上厚は10mmで
あり、引張強度およびせん断強さ試験片は何れも
圧延直角方向から採取した。[Table] The heating temperature was 1250℃, and then the original thickness was rolled using various combinations of base materials and composite materials as shown in Table 2 under the rolling conditions shown in Table 2. The mechanical properties are also shown in this Table 2. In each pass schedule, the finishing temperature was 700°C, the finishing thickness was 10 mm, and the tensile strength and shear strength test pieces were taken from the direction perpendicular to the rolling direction.
【表】【table】
【表】
第2図には接合粗圧下率と950〜650℃の累積圧
下率(CR率)を変化させた場合のせん断強さを
示すが、せん断強さを20Kg/mm2以上に保持するた
めに必要な下限粗圧下率および上限累積圧下率が
存在する。前記第2表におけるNo.15のものは母材
炭素量が上限炭素量を超えた組合わせにおいて本
発明の標準的な圧延を行つたものであり、剪断強
さの著しい低下が認められる。
No.6、No.10およびNo.14のものは接合粗圧下率、
CR率が何れも高く靭性に優れていてもせん断強
さにおいて大幅に劣つている。このことはNo.16お
よびNo.17或いはNo.21、22のものでも同様である。
これに対しNo.18、19或いはNo.24、25のものはせん
断強さに優れているけれども靭性において劣つて
いることが明かで、何れも本発明の目的を達し得
ない。
本発明の条件を満足したNo.4、5、No.7〜9、
No.11〜13およびNo.20のものは何れも靭性において
−℃であり、しかもせん断強さは25Kg/mm2以上で
靭性とせん断強さが共に優れており、好ましいク
ラツド材であることは明かである。
なお本発明方法は、炭素鋼とステンレス鋼の間
に、(a)Ni等のインサート材を含まない場合、(b)
最終製品において0〜50μの厚みをもつNi等のイ
ンサート材を含む場合の双方の場合に適用するこ
とができ、この程度の厚みのNiなどによるイン
サート材を含む場合でもステンレス鋼の界面にお
けるクロム炭化物の析出挙動はインサート材を含
まない場合に比較して大きな差が認められない。
又本発明でいうオーステナイト・ステンレス鋼と
は炭素含有量以外については特に特定するものが
なく、一般的に認識されているものを言う。即ち
Si:2%以下、Mn:5%以下、Ni:6〜50%、
Cr:10〜30%、Al:1%以下で残部が鉄および
不可避不純物から成る鋼を基本組成として、必要
に応じて更にTi:2%以下、Nb:2%以下、
Cu:4%以下、Mo:10%以下の1種又は2種以
上を添加含有した鋼などが含まれる。又本発明で
いう炭素鋼も炭素含有量以外は特に規定する必要
はないが、Si:0.10〜0.70%、Mn:0.20〜2.00
%、so1.Al:0.07%以下で残部が鉄および不可避
不純物から成る鋼を基本組成とし、必要に応じて
これにNb:0.20%以下、V:0.30%以下、Zr:
0.20%以下、Ti:0.30%以下、Ta:0.10%以下、
B:0.002%以下、Mo:0.6%以下、Cu:1.0%以
下、Ni:3.0%以下の何れか1種又は2種以上を
添加含有した鋼などを示すものである。これらの
オーステナイトステンレス鋼、炭素鋼について本
発明によるものが同様に適用し、所期の作用効果
を発揮し得ることは実験的に充分確認できる。
以上説明したような本発明によるときは苛酷な
使用条件に耐える高靭性でステンレス材による高
耐食性を適切に具備したクラツド鋼板を制御圧延
法を用い、クロム炭化物の析出を抑制し、又充分
な接合強度をもつたクラツド材として適切に製造
し得るものであり、それによつてサワーガスなど
の環境下に使用されるに適した好ましい各種製品
を必要し得るものであるから工業的にその効果の
大きい発明である。[Table] Figure 2 shows the shear strength when the rough joint reduction rate and the cumulative reduction rate (CR rate) from 950 to 650℃ are changed. There is a lower limit crude reduction rate and an upper limit cumulative reduction rate necessary for this purpose. In the case of No. 15 in Table 2 above, the standard rolling of the present invention was performed in a combination in which the base material carbon content exceeded the upper limit carbon content, and a significant decrease in shear strength was observed. No. 6, No. 10 and No. 14 have rough joint reduction ratio,
Even though the CR ratio is high and the toughness is excellent, the shear strength is significantly inferior. This also applies to Nos. 16 and 17, or Nos. 21 and 22.
On the other hand, although Nos. 18 and 19 or Nos. 24 and 25 have excellent shear strength, it is clear that they are inferior in toughness, and neither of them can achieve the object of the present invention. Nos. 4, 5, Nos. 7 to 9, which satisfied the conditions of the present invention,
Nos. 11 to 13 and No. 20 all have a toughness of -℃ and a shear strength of 25 kg/mm 2 or more, which indicates that they are excellent in both toughness and shear strength, making them desirable cladding materials. It's obvious. Note that the method of the present invention is applicable to cases where (a) insert material such as Ni is not included between carbon steel and stainless steel, and (b)
It can be applied to both cases where the final product contains an insert material such as Ni with a thickness of 0 to 50 μm, and even if the final product contains an insert material such as Ni with a thickness of this level, chromium carbide at the interface of stainless steel There is no significant difference in the precipitation behavior compared to the case without insert material.
Furthermore, the austenitic stainless steel referred to in the present invention refers to a generally recognized stainless steel with no particular specification other than carbon content. That is,
Si: 2% or less, Mn: 5% or less, Ni: 6 to 50%,
The basic composition is steel consisting of Cr: 10 to 30%, Al: 1% or less, the balance being iron and unavoidable impurities, and if necessary, further Ti: 2% or less, Nb: 2% or less,
Steels containing one or more of Cu: 4% or less and Mo: 10% or less are included. Also, the carbon steel referred to in the present invention does not need to be specified except for the carbon content, but Si: 0.10 to 0.70%, Mn: 0.20 to 2.00%.
%, so1.The basic composition is steel with Al: 0.07% or less and the balance consisting of iron and unavoidable impurities, and if necessary, Nb: 0.20% or less, V: 0.30% or less, Zr:
0.20% or less, Ti: 0.30% or less, Ta: 0.10% or less,
This refers to steel containing one or more of the following: B: 0.002% or less, Mo: 0.6% or less, Cu: 1.0% or less, and Ni: 3.0% or less. It has been fully confirmed experimentally that the present invention can be similarly applied to these austenitic stainless steels and carbon steels and can exhibit the desired effects. According to the present invention as explained above, a clad steel plate having high toughness that can withstand severe usage conditions and suitably having high corrosion resistance due to stainless steel is rolled using a controlled rolling method, suppressing precipitation of chromium carbide, and achieving sufficient bonding. This invention has great industrial effects because it can be suitably manufactured as a cladding material with strength, and as a result, various desirable products suitable for use in environments such as sour gas are required. It is.
図面は本発明の技術的内容を示すものであつ
て、第1図は接合粗圧下率とCR率との関係での
本発明方法の範囲を示した図表、第2図は接合粗
圧下率とCR率に対するせん断強さ20Kg/mm2以上
の範囲を示した図表である。
The drawings show the technical contents of the present invention. Figure 1 is a chart showing the range of the method of the present invention in relation to the rough joint reduction rate and CR rate, and Figure 2 is a graph showing the range of the method of the present invention in relation to the rough joint reduction rate and CR rate. This is a chart showing the range of shear strength of 20 Kg/mm 2 or more with respect to CR rate.
Claims (1)
部材を重ね合せて圧延しクラツド鋼板を製造する
に当つて、前記炭素鋼の炭素含有量を0.12%以下
とすると共にオーステナイトステンレス鋼の炭素
含有量を0.052%以下となし、しかも1000〜1250
℃の温度域においては下記する式の関係を満す
接合粗圧下率による圧延を行い、又650〜950℃の
温度域においては下記式の関係を満す累積圧下
率による圧延を行うことを特徴とする高靭性高耐
食性クラツド鋼板の製造方法。 接合粗圧下率(%)≧15%+0.2×〔CR率(%)〕…
20%≦CR率≦〔90%−200×{炭素鋼の含有炭素量(w
t%)}〕… 但し上記、式においてCR率は650〜950℃
の温度域における累積圧下率を示すものである。[Scope of Claims] 1. In producing a clad steel plate by stacking and rolling members made of carbon steel and austenitic stainless steel, the carbon content of the carbon steel is set to 0.12% or less, and the carbon content of the austenitic stainless steel is The amount should be 0.052% or less, and 1000 to 1250
In the temperature range of 650 to 950 degrees Celsius, rolling is performed with a joint rough reduction rate that satisfies the relationship of the following formula, and in the temperature range of 650 to 950 degrees Celsius, rolling is performed with a cumulative reduction rate that satisfies the relationship of the following formula. A method for manufacturing a high-toughness, high-corrosion-resistant clad steel sheet. Rough joint reduction rate (%) ≧ 15% + 0.2 × [CR rate (%)]...
20% ≦ CR rate ≦ [90% − 200 × {carbon content of carbon steel (w
t%)}]... However, in the above formula, the CR rate is 650 to 950℃
This shows the cumulative rolling reduction rate in the temperature range.
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP56201512A JPS58103986A (en) | 1981-12-16 | 1981-12-16 | Production of high toughness high corrosion resistance clad steel plate |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP56201512A JPS58103986A (en) | 1981-12-16 | 1981-12-16 | Production of high toughness high corrosion resistance clad steel plate |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| JPS58103986A JPS58103986A (en) | 1983-06-21 |
| JPH0241400B2 true JPH0241400B2 (en) | 1990-09-17 |
Family
ID=16442266
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP56201512A Granted JPS58103986A (en) | 1981-12-16 | 1981-12-16 | Production of high toughness high corrosion resistance clad steel plate |
Country Status (1)
| Country | Link |
|---|---|
| JP (1) | JPS58103986A (en) |
Cited By (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| WO2021124759A1 (en) | 2019-12-19 | 2021-06-24 | 大日本印刷株式会社 | Laminate, medium, and method |
| WO2022102751A1 (en) | 2020-11-13 | 2022-05-19 | 大日本印刷株式会社 | Laminate, print product, and method using laminate |
Family Cites Families (9)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JP2005041623A (en) * | 2003-07-25 | 2005-02-17 | Fuji Xerox Co Ltd | Carrying device and image forming device |
| JP2007058079A (en) * | 2005-08-26 | 2007-03-08 | Canon Inc | Image forming apparatus |
| JP2007139882A (en) * | 2005-11-15 | 2007-06-07 | Ricoh Co Ltd | Image forming method and image forming apparatus |
| JP2009251237A (en) * | 2008-04-04 | 2009-10-29 | Ricoh Co Ltd | Image forming apparatus |
| JP5621383B2 (en) * | 2009-09-11 | 2014-11-12 | 株式会社リコー | Conveying apparatus, image forming apparatus, conveyed medium conveying method, program |
| US20110262163A1 (en) * | 2010-04-21 | 2011-10-27 | Toshiba Tec Kabushiki Kaisha | Image transfer position adjustment |
| JP2012096852A (en) * | 2010-10-29 | 2012-05-24 | Konica Minolta Business Technologies Inc | Paper conveying apparatus and image forming system |
| JP5917014B2 (en) * | 2011-04-20 | 2016-05-11 | キヤノン株式会社 | Image forming apparatus |
| JP6427857B2 (en) * | 2013-07-17 | 2018-11-28 | 株式会社リコー | Displacement measuring device, displacement measuring method, and image forming apparatus |
-
1981
- 1981-12-16 JP JP56201512A patent/JPS58103986A/en active Granted
Cited By (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| WO2021124759A1 (en) | 2019-12-19 | 2021-06-24 | 大日本印刷株式会社 | Laminate, medium, and method |
| WO2022102751A1 (en) | 2020-11-13 | 2022-05-19 | 大日本印刷株式会社 | Laminate, print product, and method using laminate |
Also Published As
| Publication number | Publication date |
|---|---|
| JPS58103986A (en) | 1983-06-21 |
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