JPH07126795A - Work roll for hot rolling - Google Patents
Work roll for hot rollingInfo
- Publication number
- JPH07126795A JPH07126795A JP30108293A JP30108293A JPH07126795A JP H07126795 A JPH07126795 A JP H07126795A JP 30108293 A JP30108293 A JP 30108293A JP 30108293 A JP30108293 A JP 30108293A JP H07126795 A JPH07126795 A JP H07126795A
- Authority
- JP
- Japan
- Prior art keywords
- outer shell
- roll
- shell layer
- resistance
- hot rolling
- 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.)
- Granted
Links
- 238000005098 hot rolling Methods 0.000 title abstract description 15
- 229910001208 Crucible steel Inorganic materials 0.000 claims abstract description 17
- 229910052804 chromium Inorganic materials 0.000 claims abstract description 14
- 229910001141 Ductile iron Inorganic materials 0.000 claims abstract description 12
- 229910052750 molybdenum Inorganic materials 0.000 claims abstract description 11
- 229910052720 vanadium Inorganic materials 0.000 claims abstract description 11
- 229910052759 nickel Inorganic materials 0.000 claims abstract description 9
- 229910052748 manganese Inorganic materials 0.000 claims abstract description 8
- 238000009750 centrifugal casting Methods 0.000 claims abstract description 6
- 239000002184 metal Substances 0.000 claims description 13
- 229910052751 metal Inorganic materials 0.000 claims description 13
- 238000005096 rolling process Methods 0.000 claims description 10
- 239000000203 mixture Substances 0.000 claims description 9
- XEEYBQQBJWHFJM-UHFFFAOYSA-N iron Substances [Fe] XEEYBQQBJWHFJM-UHFFFAOYSA-N 0.000 claims description 5
- 229910052742 iron Inorganic materials 0.000 claims description 3
- 238000005266 casting Methods 0.000 abstract description 15
- 239000000463 material Substances 0.000 abstract description 14
- 229910052799 carbon Inorganic materials 0.000 abstract description 9
- 238000007788 roughening Methods 0.000 abstract description 4
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 abstract description 3
- 238000004519 manufacturing process Methods 0.000 abstract description 3
- 238000010791 quenching Methods 0.000 abstract description 3
- 230000000171 quenching effect Effects 0.000 abstract description 3
- 238000005496 tempering Methods 0.000 abstract description 3
- 229910000831 Steel Inorganic materials 0.000 abstract description 2
- 239000010959 steel Substances 0.000 abstract description 2
- 239000011651 chromium Substances 0.000 abstract 3
- 229920002165 CarbonCast Polymers 0.000 abstract 2
- VYZAMTAEIAYCRO-UHFFFAOYSA-N Chromium Chemical compound [Cr] VYZAMTAEIAYCRO-UHFFFAOYSA-N 0.000 abstract 2
- 238000010030 laminating Methods 0.000 abstract 1
- 230000000694 effects Effects 0.000 description 23
- 239000011162 core material Substances 0.000 description 14
- 229910001018 Cast iron Inorganic materials 0.000 description 12
- 150000001247 metal acetylides Chemical class 0.000 description 11
- 238000012360 testing method Methods 0.000 description 10
- PXHVJJICTQNCMI-UHFFFAOYSA-N Nickel Chemical compound [Ni] PXHVJJICTQNCMI-UHFFFAOYSA-N 0.000 description 9
- 239000011159 matrix material Substances 0.000 description 9
- 230000000052 comparative effect Effects 0.000 description 8
- 230000006872 improvement Effects 0.000 description 8
- 229910001566 austenite Inorganic materials 0.000 description 5
- 230000006866 deterioration Effects 0.000 description 5
- 238000010438 heat treatment Methods 0.000 description 5
- 238000000034 method Methods 0.000 description 5
- 230000008569 process Effects 0.000 description 5
- 238000005452 bending Methods 0.000 description 4
- 238000001816 cooling Methods 0.000 description 4
- 239000003795 chemical substances by application Substances 0.000 description 3
- 238000009792 diffusion process Methods 0.000 description 3
- 238000002844 melting Methods 0.000 description 3
- 230000008018 melting Effects 0.000 description 3
- 238000002156 mixing Methods 0.000 description 3
- 239000006104 solid solution Substances 0.000 description 3
- 238000007711 solidification Methods 0.000 description 3
- 230000008023 solidification Effects 0.000 description 3
- 230000003746 surface roughness Effects 0.000 description 3
- 241000723353 Chrysanthemum Species 0.000 description 2
- 235000007516 Chrysanthemum Nutrition 0.000 description 2
- 238000005299 abrasion Methods 0.000 description 2
- 230000004888 barrier function Effects 0.000 description 2
- 230000015572 biosynthetic process Effects 0.000 description 2
- 239000013078 crystal Substances 0.000 description 2
- 238000002425 crystallisation Methods 0.000 description 2
- 230000008025 crystallization Effects 0.000 description 2
- 210000001787 dendrite Anatomy 0.000 description 2
- 230000001771 impaired effect Effects 0.000 description 2
- 239000012535 impurity Substances 0.000 description 2
- 238000003754 machining Methods 0.000 description 2
- 238000001000 micrograph Methods 0.000 description 2
- 230000000717 retained effect Effects 0.000 description 2
- 230000006641 stabilisation Effects 0.000 description 2
- 238000011105 stabilization Methods 0.000 description 2
- 239000000126 substance Substances 0.000 description 2
- 238000004227 thermal cracking Methods 0.000 description 2
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 1
- GRYLNZFGIOXLOG-UHFFFAOYSA-N Nitric acid Chemical compound O[N+]([O-])=O GRYLNZFGIOXLOG-UHFFFAOYSA-N 0.000 description 1
- 230000009471 action Effects 0.000 description 1
- 230000008602 contraction Effects 0.000 description 1
- 238000005336 cracking Methods 0.000 description 1
- 238000005516 engineering process Methods 0.000 description 1
- 238000005530 etching Methods 0.000 description 1
- 229910002804 graphite Inorganic materials 0.000 description 1
- 239000010439 graphite Substances 0.000 description 1
- 230000005484 gravity Effects 0.000 description 1
- 230000009545 invasion Effects 0.000 description 1
- 238000012423 maintenance Methods 0.000 description 1
- 229910017604 nitric acid Inorganic materials 0.000 description 1
- 230000002250 progressing effect Effects 0.000 description 1
- 230000009467 reduction Effects 0.000 description 1
- 238000007670 refining Methods 0.000 description 1
- 230000001105 regulatory effect Effects 0.000 description 1
- 239000004576 sand Substances 0.000 description 1
- 238000000926 separation method Methods 0.000 description 1
- 238000005728 strengthening Methods 0.000 description 1
- 210000001550 testis Anatomy 0.000 description 1
- 230000008646 thermal stress Effects 0.000 description 1
- 239000002699 waste material Substances 0.000 description 1
Landscapes
- Reduction Rolling/Reduction Stand/Operation Of Reduction Machine (AREA)
Abstract
Description
【0001】[0001]
【産業上の利用分野】本発明は、ホットストリップミル
等の鋼材の熱間圧延に使用されるワークロールの耐摩耗
性、耐肌荒れ性、耐熱亀裂性、耐スリップ性等の改良に
関する。BACKGROUND OF THE INVENTION 1. Field of the Invention The present invention relates to improvements in wear resistance, surface roughening resistance, heat crack resistance, slip resistance and the like of work rolls used for hot rolling of steel materials such as hot strip mills.
【0002】[0002]
【従来の技術】ホットストリップミル等の熱間圧延装置
におけるワークロールは、熱延操業の円滑な遂行および
被圧延材の品質確保のために、圧延荷重のベンディング
に抗し得る強靱性と共に、摩耗,肌荒れ,熱亀裂等に対
する抵抗性を具備するものであることが要求される。ア
ダマイト鋳鉄,ニッケルグレン鋳鉄,ダクタイル鋳鉄等
は、従来より使用されてきた代表的なロール材料である
が、それぞれ一長一短を有し、耐摩耗性,耐肌荒れ性,
耐熱亀裂性等の諸特性の全てを満足し得るものとはいい
難い。Work rolls used in hot strip mills such as hot strip mills have a toughness that can withstand bending of rolling load and wear in order to smoothly perform hot rolling operation and ensure quality of rolled material. It is required to have resistance to rough skin, heat cracks, etc. Adamantite cast iron, nickel grain cast iron, ductile cast iron, etc. are typical roll materials that have been used so far, but they have advantages and disadvantages, wear resistance, rough surface resistance,
It is hard to say that all the properties such as heat crack resistance can be satisfied.
【0003】近年、熱延用ワークロールとして、高C−
高Cr鋳鉄ロールが多く使用されるようになり、特開昭
58-30382号公報には、図1に示すように、ロールを外殻
層1と、中間層2と、軸芯材3からなる積層構造体と
し、外殻層1に高C- 高Cr鋳鉄を適用し、中間層2を
介して軸芯材3をダクタイル鋳鉄で形成したロールが提
案されている。この積層構造を有するロールは、外殻層
1の高C−高Cr鋳鉄(基地中にM7 C3 型の硬いCr
系炭化物が多量に分散した組織を有する)によりロール
表面に高度の摩耗抵抗性を持たせる一方、ダクタイル鋳
鉄からなる軸芯材3で圧延荷重のベンディングに抗する
強靱性を保証し、また外殻層1(Cr等の炭化物形成元
素を多量に含む)から軸芯材3(ダクタイル鋳鉄)にC
r等の炭化物形成元素が拡散・混入することによる軸芯
材3の劣化(強靱性の低下)を防止するためのバリアー
層として中間層2を設けて、所要の強靱性を保持するよ
うにしている。In recent years, as a work roll for hot rolling, high C-
High Cr cast iron rolls have been widely used, and
In JP 58-30382, as shown in FIG. 1, a roll is a laminated structure composed of an outer shell layer 1, an intermediate layer 2 and a mandrel 3, and the outer shell layer 1 is made of high C-high Cr cast iron. And a roll in which the shaft core material 3 is formed of ductile cast iron via the intermediate layer 2 is proposed. The roll having this laminated structure is made of high C-high Cr cast iron of the outer shell layer 1 (M 7 C 3 type hard Cr in the matrix).
The roll surface has a high degree of wear resistance by virtue of having a structure in which a large amount of system carbides are dispersed), while the shaft core material 3 made of ductile cast iron guarantees toughness that resists bending of rolling load, and the outer shell From layer 1 (containing a large amount of carbide forming elements such as Cr) to shaft core material 3 (ductile cast iron)
The intermediate layer 2 is provided as a barrier layer for preventing deterioration (decrease in toughness) of the mandrel 3 due to diffusion and mixing of a carbide forming element such as r, so that required toughness is maintained. There is.
【0004】[0004]
【発明が解決しようとする課題】熱間圧延ロールの外殻
層を高C−高Cr鋳鉄で形成した上記積層構造ロール
は、熱的・機械的負荷の大きい粗圧延スタンドへ適用し
た場合にも、アダマイト鋳鉄ロール等の従来ロールを凌
ぐ良好な耐摩耗性を示す。しかし、肌荒れ,熱亀裂,欠
け落ち等に対する抵抗性は充分なものといえず、また被
圧延材とのスリップを生じ易いという問題がある。本発
明者等の研究によれば、表面特性に関する上記問題は、
外殻層を形成する高C−高Cr鋳鉄が、M7 C3 型のC
r炭化物を多量に含む粗大な組織を有することに起因し
ている。すなわち、肌荒れを生じ易いのは、組織が粗大
なため、熱的・機械的負荷の大きい熱延条件下での組織
流動に対する抵抗性が低いからであり、熱亀裂を生じ易
いのは、その組織に占める硬質のM7 C3 型Cr炭化物
量(面積率)が、約20〜30%と高いために、充分な
靱性を確保し得ないことによるのであり、また多量の硬
質炭化物を含んでいるため、実機使用過程でのロール表
面粗度が小さく、このことが被圧延材とのスリップを生
じ易い原因となっている。しかもM7 C3 型Cr炭化物
は、所謂菊花弁状の粗大な形態をなしているため、高圧
下・高熱負荷条件の圧延過程でロール表面から剥離・脱
落する欠け落ちの現象を生じ易い。近時の熱延操業は、
生産性の向上等の要請から、高圧下・高熱負荷の傾向が
進み、それに伴つて上記問題はより顕著となりつつあ
る。本発明は上記積層構造を有する熱延ロールについ
て、高圧下・高熱負荷の操業条件に耐え得る強靱性およ
び耐摩耗性を始めとする上記諸特性を高め、ロール耐用
寿命および被圧延材品質の向上・安定化を可能とする改
良された熱延ロールを提供しようとするものである。The above-mentioned laminated structure roll in which the outer shell layer of the hot rolling roll is made of high C-high Cr cast iron is applied to a rough rolling stand having a large thermal and mechanical load. Exhibits excellent wear resistance over conventional rolls such as adamite cast iron rolls. However, the resistance to rough skin, thermal cracking, chipping and the like cannot be said to be sufficient, and there is a problem that slippage with the material to be rolled easily occurs. According to the study by the present inventors, the above-mentioned problems regarding surface characteristics are
High C-high Cr cast iron forming the outer shell layer is M 7 C 3 type C
This is due to having a coarse structure containing a large amount of r carbide. That is, rough skin is likely to occur because the texture is coarse and resistance to tissue flow under hot rolling conditions with large thermal and mechanical loads is low, and thermal cracking is likely to occur in the texture. This is because the amount of hard M 7 C 3 type Cr carbide (area ratio) occupying 20% to 30% is high, so that sufficient toughness cannot be secured, and a large amount of hard carbide is included. Therefore, the roll surface roughness is small in the process of using the actual machine, which causes slipping with the material to be rolled. Moreover, since the M 7 C 3 type Cr carbide has a so-called chrysanthemum petal-like coarse shape, a phenomenon of peeling and falling off from the roll surface is likely to occur during the rolling process under high pressure and high heat load conditions. Recent hot rolling operations are
Due to the demand for improved productivity, the trend of high pressure and high heat load is progressing, and the above problems are becoming more prominent. The present invention, with respect to the hot rolled roll having the above-mentioned laminated structure, enhances the above-mentioned characteristics including toughness and wear resistance capable of withstanding operating conditions under high pressure and high heat load, and improves roll life and quality of rolled material. -It is intended to provide an improved hot rolling roll that enables stabilization.
【0005】[0005]
【課題を解決するための手段】本発明の熱間圧延用ロー
ルは、遠心力鋳造により積層形成された外殻層と中間
層、および中間層の内側に鋳造された軸芯材とからなる
積層構造を有し、外殻層は、C:0.8〜1.2%,S
i:0.5〜1.5%,Mn:0.5〜1.5%,C
r:3.0〜12.0%,Mo:1.0〜3.0%,
V:0.5〜2.0%,Ni:0.5〜2.0%,残部
実質的にFeからなる溶湯組成を有する鋳鋼からなり、
中間層は、C:1.0〜2.0%,Si:1.5〜2.
5%,Mn:1.0%以下,Ni:1.0%以下,残部
実質的にFeからなる溶湯組成を有する鋳鋼からなり、
軸芯材はダクタイル鋳鉄からなる、ことを特徴としてい
る。A roll for hot rolling according to the present invention is a laminate comprising an outer shell layer and an intermediate layer laminated by centrifugal casting, and a shaft core material cast inside the intermediate layer. The outer shell layer has a structure of C: 0.8 to 1.2%, S
i: 0.5 to 1.5%, Mn: 0.5 to 1.5%, C
r: 3.0 to 12.0%, Mo: 1.0 to 3.0%,
V: 0.5 to 2.0%, Ni: 0.5 to 2.0%, the balance being cast steel having a molten metal composition consisting essentially of Fe,
The intermediate layer has C: 1.0 to 2.0% and Si: 1.5 to 2.
5%, Mn: 1.0% or less, Ni: 1.0% or less, the balance being cast steel having a molten metal composition consisting essentially of Fe,
The shaft core material is made of ductile cast iron.
【0006】[0006]
【作用】本発明の熱延ロールの外殻層を形成する鋳鋼
は、高C−高Cr鋳鉄に比べ、C量が少なく、また炭化
物形成元素であるCr量を少なくする一方において、V
を一定量含有する組成に調整されている。CrとCの結
合により形成されるM7 C3 型炭化物〔(Fe,Cr)
7 C3 〕は、前記のように菊花弁状の粗大な晶出形態を
呈するのに対し、VとCが結合して形成されるMC型の
VC炭化物の晶出形態は微細かつ均一である。本発明ロ
ールの外殻層は、鋳造溶湯の降温凝固過程でVC炭化物
が微細に晶出する効果として、デンドライトの成長が抑
制され、オーステナイト結晶粒が微細化される。更にそ
の結晶粒の微細化に伴つて、粒界に生成するM7 C3 型
Cr炭化物も微細化される。この組織の微細化効果とし
て、高圧下・高熱負荷の実機使用における組織流動に対
する高い抵抗性が付与され、良好な耐肌荒れ性を示す。
またC量が少量に規制されているので、炭化物の生成量
が少なく、組織中に占める比率(面積率)は約8%以下
となり、従って靱性に富み、熱応力によるクラックの発
生・伝播に対する抵抗性が高く、耐熱亀裂性に優れてい
る。更に、組織中に占める炭化物量が抑制されている効
果として、ロールの実機使用過程において被圧延材との
スリップを回避するに必要な適度の表面粗度が付与され
る。しかも、その炭化物は微細な晶出形態を有している
ので、実機使用過程での耐欠け落ち性にも優れている。The cast steel forming the outer shell layer of the hot-rolled roll of the present invention has a small amount of C and a small amount of Cr, which is a carbide forming element, as compared with the high C-high Cr cast iron.
Is adjusted to a composition containing a certain amount. M 7 C 3 type carbide [(Fe, Cr) formed by combining Cr and C
7 C 3 ] has a coarse chrysanthemum petal-like crystallized form as described above, whereas the crystallized form of MC-type VC carbide formed by combining V and C is fine and uniform. . In the outer shell layer of the roll of the present invention, the dendrite growth is suppressed and the austenite crystal grains are miniaturized, as an effect of finely crystallizing VC carbides during the temperature-lowering solidification process of the casting melt. Further, along with the refinement of the crystal grains, the M 7 C 3 type Cr carbide generated at the grain boundaries is also refined. As a micronization effect of this structure, high resistance to tissue flow under high pressure / high heat load is actually imparted, and good resistance to rough skin is exhibited.
Also, since the amount of C is regulated to a small amount, the amount of carbides generated is small, and the ratio (area ratio) in the structure is about 8% or less. Therefore, it is rich in toughness and has resistance to the generation and propagation of cracks due to thermal stress. It has high resistance to heat cracking. Further, as an effect of suppressing the amount of carbides occupying in the structure, an appropriate surface roughness required to avoid slip with the material to be rolled is imparted in the process of using the roll in an actual machine. Moreover, since the carbide has a fine crystallized morphology, it has excellent chipping resistance in the process of actual use.
【0007】本発明のロールは、外殻層の炭化物量を上
記のように少量に抑制していながら、高度の摩耗抵抗性
を併せ有している。これは、VC炭化物が、マイクロビ
ッカース硬さHvで約2400〜3400と、Cr炭化物〔(F
e,Cr)7 C3 〕のHv約1800〜2500に比べて著しく
高く、この高硬度炭化物が基地中に微細に分散している
効果として、炭化物の総量が少ないにも拘らず、高C-
高Cr鋳鉄と同等ないしそれを超える高度の耐摩耗性を
確保することを可能にしているのである。なお、外殻層
(Cr,Mo,V等の炭化物形成元素を含む)から、そ
の炭化物形成元素が、ダクタイル鋳鉄からなる軸芯材に
拡散・混入すると、軸芯材の強靱性を損なう原因となる
が、本発明では、外殻層のCr含有量が比較的低いの
で、外殻層からの拡散・混入はそれだけ少なく、かつそ
の拡散・侵入は中間層をバリアーとして効果的に抑制防
止され、従って高圧延荷重のベンディングに抗するため
の軸芯材の強度・靱性は十分に確保される。The roll of the present invention has a high degree of abrasion resistance while suppressing the amount of carbide in the outer shell layer to a small amount as described above. This is because VC carbide has a micro Vickers hardness Hv of about 2400 to 3400 and Cr carbide [(F
e, Cr) 7 C 3 ], which is significantly higher than Hv of about 1800 to 2500, and the effect of finely dispersing this high hardness carbide in the matrix is that although the total amount of carbide is small, high C-
This makes it possible to ensure a high level of wear resistance equivalent to or higher than that of high Cr cast iron. In addition, if the carbide forming element diffuses and mixes into the shaft core material made of ductile cast iron from the outer shell layer (including carbide forming elements such as Cr, Mo, V), it causes the deterioration of the toughness of the shaft core material. However, in the present invention, since the Cr content of the outer shell layer is relatively low, the diffusion and mixing from the outer shell layer is so small, and the diffusion and invasion are effectively suppressed and prevented by using the intermediate layer as a barrier, Therefore, the strength and toughness of the shaft core material against the bending of a high rolling load are sufficiently secured.
【0008】以下、本発明のロールについて、まず外殻
層の鋳鋼溶湯の成分限定理由を説明する。 C:0.8〜1.2% Cは、Cr,Mo,V等と結合して炭化物を形成し、耐
摩耗性の向上に寄与する。0.8%に満たないと、炭化
物の生成量が不足し、耐摩耗性を充分に高めることがで
きない。他方1.2%を超えると、炭化物の過剰生成に
より、靱性が低下し、耐熱亀裂性が損なわれる。With respect to the roll of the present invention, the reasons for limiting the components of the molten cast steel of the outer shell layer will be described below. C: 0.8 to 1.2% C combines with Cr, Mo, V, etc. to form a carbide, which contributes to the improvement of wear resistance. If it is less than 0.8%, the amount of carbide formed is insufficient and the wear resistance cannot be sufficiently enhanced. On the other hand, if it exceeds 1.2%, the toughness is lowered due to excessive formation of carbides, and the heat crack resistance is impaired.
【0009】Si:0.5〜1.5% Siは、鋳鋼溶湯の脱酸剤として添加される。その量が
0.5%に満たないと、脱酸効果が不足し、他方1.5
%を超えると、脆化を招き、耐熱亀裂性が低下する。Si: 0.5 to 1.5% Si is added as a deoxidizing agent for molten cast steel. If the amount is less than 0.5%, the deoxidizing effect is insufficient, while 1.5%
If it exceeds%, embrittlement is caused and the heat crack resistance is lowered.
【0010】Mn:0.5〜1.5% Mnは、鋳鋼溶湯の脱酸剤として、また不純分であるS
をMnSとして固定無害化する元素として、少なくとも
0.5%を必要とする。しかし、1.5%を超えると、
残留オーステナイトが生じ易くなり、硬度・耐摩耗性の
不足を招く。Mn: 0.5-1.5% Mn is a deoxidizing agent for the molten cast steel and is an impurity of S.
As MnS, at least 0.5% is required as an element for fixing and detoxifying. However, if it exceeds 1.5%,
Residual austenite is likely to occur, resulting in insufficient hardness and wear resistance.
【0011】Cr:3.0〜12.0% Crは、基地中に固溶して基地を強化し、一部はCr系
炭化物を形成して耐摩耗性の向上に寄与する。この効果
を得るために少なくとも3.0%を必要とする。添加増
量により効果を増すが、12.0%を超えると、Cr系
炭化物の生成量が不必要に増量すると共に、高硬度を有
する微細なVC炭化物の生成量の不足をきたし、靱性の
低下とそれに伴う耐肌荒れ性の低下等の不具合を招く。Cr: 3.0 to 12.0% Cr forms a solid solution in the matrix to strengthen the matrix, and partially forms a Cr-based carbide to contribute to the improvement of wear resistance. At least 3.0% is required to obtain this effect. The effect is increased by increasing the amount of addition, but if it exceeds 12.0%, the amount of Cr-based carbides is unnecessarily increased, and the amount of fine VC carbides with high hardness is insufficiently generated, resulting in a decrease in toughness. As a result, problems such as deterioration of the rough skin resistance are caused.
【0012】Mo:1.0〜3.0% Moは、基地中に固溶して焼入れ性の向上および焼戻し
脆性の防止に奏効し、かつ高温特性の改善効果を有する
ほか、その一部はMo系炭化物を形成して耐摩耗性の向
上に寄与する。これらの効果を確保するためには、少な
くとも1.0%を必要とする。添加増量に伴い効果を増
すが、3.0%を超えると、過飽和となり、それ以上の
添加は無駄であるばかりか、残留オーステナイトの安定
化を招き、硬度・耐摩耗性の不足をきたす原因となる。Mo: 1.0 to 3.0% Mo is effective as a solid solution in the matrix to improve hardenability and prevent temper embrittlement, and also has an effect of improving high temperature characteristics. It forms a Mo-based carbide and contributes to the improvement of wear resistance. To secure these effects, at least 1.0% is required. The effect increases with increasing the amount of addition, but if it exceeds 3.0%, it becomes supersaturated, and addition beyond that is not only a waste, but also leads to stabilization of retained austenite, causing a lack of hardness and wear resistance. Become.
【0013】V:0.5〜2.0% Vは、Cと結合して微細で高硬度のVC炭化物を形成す
ることにより、耐摩耗性の向上に最も寄与する元素であ
る。そのMC型炭化物は、高C−高Cr鋳鉄の基地中に
晶出するM7 C3 型Cr炭化物に比べて著しく微細であ
り、その微細晶出の効果として、樹枝状晶の成長が抑制
され、オーステナイト結晶粒が微細化されると同時に、
粒界に生成するM7 C3 型のCr系炭化物も微細化され
る。この組織の微細・均一化により、耐肌荒れ性等の表
面特性の顕著な改善効果が達成される。上記Vの添加効
果を充分なものとするには、少なくとも0.5%を必要
とする。添加増量により効果の増加をみるが、2.0%
を超えると、炭化物生成量が過剰となると共に、遠心力
鋳造工程において、遠心力による該炭化物の比重分離が
顕著となり、上記表面特性の改善効果が損なわれる。V: 0.5 to 2.0% V is an element which contributes most to the improvement of wear resistance by forming a fine and high hardness VC carbide by combining with C. The MC type carbide is significantly finer than the M 7 C 3 type Cr carbide crystallized in the matrix of high C-high Cr cast iron, and the effect of the fine crystallization is that the growth of dendrites is suppressed. At the same time that the austenite grains are refined,
The M 7 C 3 type Cr-based carbides generated at the grain boundaries are also refined. By making the structure fine and uniform, remarkable improvement effects of surface characteristics such as resistance to roughening of the surface are achieved. At least 0.5% is required to make the effect of adding V sufficient. The effect is increased by increasing the amount added, but 2.0%
If it exceeds, the amount of carbide produced becomes excessive, and in the centrifugal casting step, the specific gravity separation of the carbide becomes remarkable due to centrifugal force, and the effect of improving the above-mentioned surface characteristics is impaired.
【0014】Ni:0.5〜2.0% Niは基地中に固溶して焼入れ性を高める効果を有す
る。0.5%に満たないと、その効果が得られず、他方
2.0%を超えると、残留オーステナイトを生じ易く、
硬度の不足をきたす原因となる。Ni: 0.5 to 2.0% Ni has the effect of forming a solid solution in the matrix to enhance the hardenability. If it is less than 0.5%, the effect cannot be obtained, while if it exceeds 2.0%, retained austenite is apt to occur,
It causes a lack of hardness.
【0015】次に、外殻層と軸芯材との層界面に形成さ
れる中間層について説明する。中間層は、前記のように
Cr,Mo,V等の炭化物形成元素が外殻層から軸芯材
に拡散・混入するのを防止する役目を有する層であるか
ら、この鋳造に使用される鋳鋼溶湯はCr,Mo,V等
の炭化物形成元素を含まず、これを付随する場合にも、
溶製技術上不可避的に混入する範囲の量(約0.05%
以下)に制限される。また、中間層は、外殻層の融点よ
り低い鋳込み温度で鋳造できることが必要である。鋳込
み温度が高くなると、その溶湯の鋳込み時の熱影響で生
じる外殻層の再溶融量が多くなるため、鋳造される中間
層のCr,Mo,V等が増量し、このことは中間層から
軸芯材に対するこれらの元素の拡散・混入量の増加とそ
の強靱性の劣化を招く原因となるからである。この中間
層を形成する鋳鋼溶湯の成分限定理由は次のとおりであ
る。Next, the intermediate layer formed at the layer interface between the outer shell layer and the mandrel will be described. As described above, the intermediate layer has a function of preventing the carbide forming elements such as Cr, Mo and V from diffusing and mixing into the shaft core material from the outer shell layer, and therefore, the cast steel used for this casting. The molten metal does not contain carbide forming elements such as Cr, Mo, V, etc.
Amount in the range that is inevitably mixed in the melting technology (about 0.05%
Limited to the following). Further, the intermediate layer needs to be castable at a casting temperature lower than the melting point of the outer shell layer. When the casting temperature becomes higher, the amount of remelting of the outer shell layer caused by the heat effect of the molten metal at the time of casting increases, so the amount of Cr, Mo, V, etc. in the cast intermediate layer increases. This is because it causes an increase in the amount of these elements diffused and mixed into the mandrel and deterioration of its toughness. The reasons for limiting the components of the molten cast steel forming the intermediate layer are as follows.
【0016】C:1.0〜2.0% Cは、鋳鋼の融点を下げ、鋳込み温度を低くする効果を
有する。1.0%に満たないと、鋳込み温度が高く、外
殻層の再溶融を抑制防止することが困難となる。他方
2.0%を上限とするのは、炭化物形成元素が拡散・混
入した場合の炭化物の生成に伴う靱性の劣化を防止する
ためである。C: 1.0 to 2.0% C has the effect of lowering the melting point of cast steel and lowering the casting temperature. If it is less than 1.0%, the casting temperature is high, and it becomes difficult to prevent and prevent remelting of the outer shell layer. On the other hand, the upper limit of 2.0% is to prevent deterioration of toughness associated with the formation of carbides when the carbide-forming elements diffuse and mix.
【0017】Si:1.5〜2.5% Siは、脱酸剤として1.5%以上を必要とする。しか
し、2.5%を超えると、脆化を招き、中間層の抗張力
の低下をきたす。Si: 1.5 to 2.5% Si requires 1.5% or more as a deoxidizing agent. However, if it exceeds 2.5%, embrittlement is caused and the tensile strength of the intermediate layer is lowered.
【0018】Mn:1.0%以下 Mnは、脱酸作用、および不純物SをMnSとして固定
化する効果を有する。この効果は、1.0%以下の量で
得ることができ、それ以上の添加を必要としない。Mn: 1.0% or less Mn has a deoxidizing effect and an effect of fixing the impurity S as MnS. This effect can be obtained in an amount of 1.0% or less, and does not require any further addition.
【0019】Ni:1.0%以下 Niは、黒鉛化と基地の強化に有効な元素である。黒鉛
の晶出は、溶湯の凝固に伴う体積収縮を緩和し引け巣の
防止に奏効する。この効果は、1.0%以下の量で得る
ことができ、それを超える添加は不要である。Ni: 1.0% or less Ni is an element effective in graphitizing and strengthening the matrix. Crystallization of graphite alleviates the volume contraction accompanying the solidification of the molten metal and is effective in preventing shrinkage cavities. This effect can be obtained in an amount of 1.0% or less, and addition beyond that is unnecessary.
【0020】上記中間層を介して形成される軸芯材はダ
クタイル鋳鉄が適用される。ダクタイル鋳鉄は、強靱性
を備えた熱延用ロール材として周知の材料であり、その
化学組成は、C:2.5〜4.0%,Si:2.5〜
3.5%,Mn:0.5%以下,Ni:0.5〜1.0
%,Cr:0.5%以下,Mg:0.02〜0.08
%,残部Feからなる。Ductile cast iron is applied to the shaft core formed through the intermediate layer. Ductile cast iron is a material well known as a roll material for hot rolling having a toughness, and its chemical composition is C: 2.5 to 4.0%, Si: 2.5 to.
3.5%, Mn: 0.5% or less, Ni: 0.5 to 1.0
%, Cr: 0.5% or less, Mg: 0.02 to 0.08
%, Balance Fe.
【0021】本発明の熱延用ワークロールは、遠心力鋳
造と、置き注ぎ鋳造の2段階の鋳造工程により製造され
る。まず横型遠心力鋳造機において、鋳型内に外殻層と
なる鋳鋼溶湯を鋳込み、遠心力の作用で鋳型内面に外殻
層を形成し、その外殻層が内面までほぼ凝固した後、中
間層となる鋳鋼溶湯を鋳込み、外殻層の内面に中間層を
積層形成する。ついで、その鋳型を直立させると共に、
鋳型の上端と下端とに砂型鋳型を付加したうえ、中間層
の内側空間内にダクタイル鋳鉄溶湯の鋳込み(置き注ぎ
鋳造)を行って軸芯材を形成する。上記鋳造により得ら
れた積層鋳造体(ロール)は、調質のための熱処理とし
て、焼入れ・焼戻し処理が施される。焼入れ処理は、温
度900〜1000℃に加熱保持したのち、急冷(強制
空冷)することにより達成され、焼戻し処理は、温度4
50〜600℃に加熱保持した後、徐冷(空冷)するこ
とにより達成される。熱処理の後、所定の機械加工が施
されて製品ロールに仕上げられる。The work roll for hot rolling of the present invention is manufactured by a two-step casting process of centrifugal force casting and decant casting. First, in a horizontal centrifugal casting machine, cast steel molten metal to be the outer shell layer is cast into the mold, the outer shell layer is formed on the inner surface of the mold by the action of centrifugal force, and after the outer shell layer has almost solidified to the inner surface, the intermediate layer Then, a cast steel molten metal is cast to form an intermediate layer on the inner surface of the outer shell layer. Then, while making the mold upright,
A sand mold is added to the upper and lower ends of the mold, and the molten core of ductile cast iron is cast (placed and cast) into the inner space of the intermediate layer to form the mandrel. The laminated cast body (roll) obtained by the above casting is subjected to quenching / tempering treatment as heat treatment for refining. The quenching treatment is achieved by heating and holding at a temperature of 900 to 1000 ° C. and then rapidly cooling (forced air cooling), and the tempering treatment is performed at a temperature of 4
It is achieved by heating and holding at 50 to 600 ° C. and then gradually cooling (air cooling). After the heat treatment, predetermined machining is performed to finish the product roll.
【0022】[0022]
〔1〕供試ロールの製造 外殻層と中間層を積層形成する遠心力鋳造と、軸芯材を
形成する置き注ぎ鋳造により、図1に示す積層鋳造体を
製造し、熱処理を施した後、仕上げ機械加工を加えて供
試ロールA(発明例)およびロールB(比較例)を得
る。ロールサイズは、胴部外径1200mm,胴長25
00mmであり、胴部の表面仕上げ粗さは、6Sであ
る。表1に、供試ロールAおよびBの各層の鋳造溶湯組
成(Wt%)および層の厚さ(mm)を示す。供試ロール
Bの外殻層の材種は高C−高Cr鋳鉄(特公昭58-30382
号公報所載の外殻層材料に相当) である。[1] Manufacture of test roll After manufacturing a laminated cast body shown in FIG. 1 by centrifugal force casting in which an outer shell layer and an intermediate layer are laminated and by pouring casting in which a shaft core material is formed, and subjecting to heat treatment Then, finish machining is applied to obtain a test roll A (invention example) and a roll B (comparative example). Roll size is 1200 mm outer diameter, 25 body length
The surface finish roughness of the body is 6S. Table 1 shows the molten metal composition (Wt%) and the layer thickness (mm) of each layer of the test rolls A and B. The grade of the outer shell layer of the test roll B is high C-high Cr cast iron (Japanese Patent Publication Sho 58-30382).
(Corresponding to the material of the outer shell layer described in the publication).
【0023】〔2〕供試ロールの表面硬さおよび外殻層
の組織 (1)表面硬さ ロールA(発明例):HS 78.5±0.6 ロールB(比較例):HS 72.3±0.7 (2)外殻層の組織 図2および図3に、ロールA(発明例)およびロールB
(比較例)の外殻層の金属組織(エッチング:5%硝酸
アルコール,10秒間)を示す(倍率 各図共、(1):×
100,(2):×400 )。図中の黒い部分はマトリックス、白
い部分は炭化物である。図3に示すロールB(比較例)
は、鋳造凝固過程で成長した樹枝状の名残りをとどめ、
炭化物粒も大きく、粗大な組織を呈している。これに対
し、図2のロールA(発明例)は、樹枝状の成長が抑制
され、微細な組織を呈している。それぞれの組織に占め
る炭化物量は下記のとおりである。 ロールA(発明例):4.8面積%(図2) ロールB(比較例):29.6面積%(図3)[2] Surface Hardness of Test Roll and Structure of Outer Shell Layer (1) Surface Hardness Roll A (Invention Example): H S 78.5 ± 0.6 Roll B (Comparative Example): H S 72.3 ± 0.7 (2) Structure of outer shell layer In FIGS. 2 and 3, roll A (invention example) and roll B are shown.
The metal structure (etching: 5% nitric acid alcohol, 10 seconds) of the outer shell layer of (Comparative Example) is shown (magnification: (1): × in each figure)
100, (2): × 400). The black part in the figure is the matrix and the white part is the carbide. Roll B shown in FIG. 3 (comparative example)
Retains the dendritic remnants that grew during the casting and solidification process,
The carbide grains are also large and have a coarse structure. On the other hand, roll A (invention example) in FIG. 2 has a dendritic growth suppressed and exhibits a fine structure. The amount of carbides in each structure is as follows. Roll A (invention example): 4.8 area% (FIG. 2) Roll B (comparative example): 29.6 area% (FIG. 3)
【0024】〔3〕実機使用試験 供試ロールAおよびBを、ホットストリップミルにおけ
る粗圧延スタンド(熱的・機械的負荷の最も大きい圧延
スタンドである)のワークロールとし、数回の実機使用
試験(各回の圧延量は、それぞれ25000〜4500
0トンである)に供し、表2に示す結果を得た。表中の
表面粗度(Rmax )および摩耗量は、試験使用後の測定
値の平均である。同表から明らかなように、比較例のロ
ールBは、胴部(外殻層表面)の肌荒れや,欠け落ち、
および被圧延材とのスリップ等が生じているのに対し、
発明例のロールAでは、肌荒れ,欠け落ち,スリップの
発生はなく、かつ摩耗減量も減少している。この優れた
耐肌荒れ性,耐スリップ性,耐欠け落ち性等は、図2に
示したように、組織が微細で、炭化物量も程良く抑制さ
れていることによるものであり、また炭化物量が抑制さ
れているにも拘らず、高度の耐摩耗性を有しているの
は、硬質のVC炭化物が微細かつ均一に分散しているこ
とによるものであって比較例のロールBとの差異は歴然
である。なお、使用試験終了後の軸芯材の化学組成を分
析した結果、Cr,Mo,V等の炭化物形成元素の増加
は微量(Cr:0.09%→0.49%、Mo:0.02%→0.12
%、V:trace→0.05%)であり、その抗張力は約43
5N/mm2 と十分なレベルを維持していることが認め
られた。[3] Test using actual machine Test rolls A and B were used as work rolls of a rough rolling stand (which is the rolling stand with the largest thermal and mechanical load) in the hot strip mill, and several testes using the actual machine were carried out. (The rolling amount of each time is 25000 to 4500, respectively.
It was subjected to 0 tons) and the results shown in Table 2 were obtained. The surface roughness (R max ) and wear amount in the table are averages of the measured values after the test use. As is clear from the table, the roll B of the comparative example has rough skin on the body (outer shell layer surface) and chipping off,
And, while slips etc. with the rolled material have occurred,
In Roll A of the invention example, the skin is not roughened, chipped off, slipped, and the abrasion loss was reduced. As shown in FIG. 2, the excellent resistance to rough skin, slip resistance, chipping resistance, etc. is due to the fact that the structure is fine and the amount of carbide is moderately suppressed. The reason why it has a high degree of wear resistance despite being suppressed is that the hard VC carbides are finely and uniformly dispersed, and the difference from the roll B of the comparative example is It is obvious. In addition, as a result of analyzing the chemical composition of the shaft core material after the end of the use test, a slight increase in carbide forming elements such as Cr, Mo and V (Cr: 0.09% → 0.49%, Mo: 0.02% → 0.12
%, V: trace → 0.05%), and the tensile strength is about 43.
It was confirmed that a sufficient level of 5 N / mm 2 was maintained.
【0025】[0025]
【表1】 [Table 1]
【0026】[0026]
【表2】 [Table 2]
【0027】[0027]
【発明の効果】本発明の熱間圧延用ワークロールは、耐
摩耗性、耐肌荒れ性、耐熱亀裂性,耐欠け落ち性、およ
び被圧延材とのスリップを略完全に防止し得る改良され
た表面特性を有すると共に、高荷重のベンディングに抗
する充分な強靱性を備えており、近時の高圧下・高熱負
荷の苛酷な使用環境において安定に使用することがで
き、耐用寿命の向上・ロールメンテナンスの軽減、ライ
ン効率の向上、および圧延品質の向上等に寄与するもの
である。The work roll for hot rolling of the present invention has been improved so as to be able to substantially completely prevent wear resistance, surface roughening resistance, heat crack resistance, chipping resistance, and slip with the material to be rolled. In addition to having surface characteristics, it has sufficient toughness to withstand high-load bending, and can be used stably under the recent severe conditions of high pressure and high heat load. It contributes to reduction of maintenance, improvement of line efficiency, and improvement of rolling quality.
【図1】ロールの積層構造を示す軸方向断面図である。FIG. 1 is an axial sectional view showing a laminated structure of a roll.
【図2】実施例におけるロールA(発明例)の外殻層の
金属組織を示す図面代用顕微鏡写真である〔(1)図は
倍率×50,(2)図は倍率×400〕。FIG. 2 is a drawing-substituting micrograph showing a metal structure of an outer shell layer of roll A (invention example) in Examples [(1) is a magnification of 50, and (2) is a magnification of 400].
【図3】実施例におけるロールB(比較例)の外殻層の
金属組織を示す図面代用顕微鏡写真である〔(1)図は
倍率×50,(2)図は倍率×400〕。FIG. 3 is a drawing-substituting micrograph showing a metal structure of an outer shell layer of Roll B (Comparative Example) in Examples [(1) is a magnification of × 50, (2) is a magnification of × 400].
1:外殻層、2:中間層、3:軸芯材。 1: Outer shell layer, 2: Middle layer, 3: Shaft core material.
───────────────────────────────────────────────────── フロントページの続き (51)Int.Cl.6 識別記号 庁内整理番号 FI 技術表示箇所 C22C 37/08 Z 38/00 301 L 302 E 38/56 ─────────────────────────────────────────────────── ─── Continuation of the front page (51) Int.Cl. 6 Identification code Office reference number FI technical display location C22C 37/08 Z 38/00 301 L 302 E 38/56
Claims (1)
と中間層、および中間層の内側に鋳造された軸芯材とか
らなる積層構造を有し、 外殻層は、C:0.8〜1.2%,Si:0.5〜1.
5%,Mn:0.5〜1.5%,Cr:3.0〜12.
0%,Mo:1.0〜3.0%,V:0.5〜2.0
%,Ni:0.5〜2.0%,残部実質的にFeからな
る溶湯組成を有する鋳鋼からなり、 中間層は、C:1.0〜2.0%,Si:1.5〜2.
5%,Mn:1.0%以下,Ni:1.0%以下,残部
実質的にFeからなる溶湯組成を有する鋳鋼からなり、 軸芯材はダクタイル鋳鉄からなる、ことを特徴とする熱
間圧延用ワークロール。1. A laminated structure comprising an outer shell layer laminated by centrifugal casting, an intermediate layer, and a mandrel cast inside the intermediate layer, wherein the outer shell layer has a C: 0. 8 to 1.2%, Si: 0.5 to 1.
5%, Mn: 0.5 to 1.5%, Cr: 3.0 to 12.
0%, Mo: 1.0 to 3.0%, V: 0.5 to 2.0
%, Ni: 0.5 to 2.0%, the balance being cast steel having a molten metal composition substantially consisting of Fe, the intermediate layer being C: 1.0 to 2.0%, Si: 1.5 to 2 .
5%, Mn: 1.0% or less, Ni: 1.0% or less, the balance is made of cast steel having a molten metal composition substantially consisting of Fe, and the mandrel is made of ductile cast iron. Work roll for rolling.
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP5301082A JP3006984B2 (en) | 1993-11-05 | 1993-11-05 | Work roll for hot rolling rough rolling stand |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP5301082A JP3006984B2 (en) | 1993-11-05 | 1993-11-05 | Work roll for hot rolling rough rolling stand |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| JPH07126795A true JPH07126795A (en) | 1995-05-16 |
| JP3006984B2 JP3006984B2 (en) | 2000-02-07 |
Family
ID=17892654
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP5301082A Expired - Fee Related JP3006984B2 (en) | 1993-11-05 | 1993-11-05 | Work roll for hot rolling rough rolling stand |
Country Status (1)
| Country | Link |
|---|---|
| JP (1) | JP3006984B2 (en) |
Cited By (7)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| EP0911421A4 (en) * | 1997-04-08 | 2000-05-31 | Nippon Steel Corp | COMPOSITE ROLLER FOR COLD ROLLING |
| CN102002644A (en) * | 2010-09-26 | 2011-04-06 | 中钢集团邢台机械轧辊有限公司 | Working roll for automobile sheet cold rolling and manufacturing method thereof |
| CN103008617A (en) * | 2012-12-27 | 2013-04-03 | 江西省科学院应用物理研究所 | Method for preparing high-speed steel composite roll for hot rolling |
| CN107891138A (en) * | 2017-11-09 | 2018-04-10 | 常州凯达重工科技有限公司 | A kind of preparation technology for being used to make the super high-vanadium high-speed steel pressure roller of corrugated metal sheet |
| CN111036873A (en) * | 2020-01-20 | 2020-04-21 | 青岛鑫盛源轧辊有限公司 | Centrifugal composite ductile iron cast steel roll and preparation method thereof |
| JP2020063485A (en) * | 2018-10-17 | 2020-04-23 | Jfeスチール株式会社 | Work roll for hot-rolling rough stand |
| CN117187601A (en) * | 2022-05-31 | 2023-12-08 | 天津重型装备工程研究有限公司 | Supporting roller of medium-broadband rolling mill and centrifugal composite casting method |
Citations (4)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JPH02258949A (en) * | 1988-12-02 | 1990-10-19 | Hitachi Metals Ltd | Wear-resistant composite roll |
| JPH03122249A (en) * | 1989-10-06 | 1991-05-24 | Kawasaki Steel Corp | Centrifugally cast high chromium roll |
| JPH03254354A (en) * | 1990-03-05 | 1991-11-13 | Fujikoo:Kk | Manufacture of looper roller in hot rolling mill |
| JPH05271855A (en) * | 1992-03-23 | 1993-10-19 | Hitachi Metals Ltd | Roll material for hot strip rolling |
-
1993
- 1993-11-05 JP JP5301082A patent/JP3006984B2/en not_active Expired - Fee Related
Patent Citations (4)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JPH02258949A (en) * | 1988-12-02 | 1990-10-19 | Hitachi Metals Ltd | Wear-resistant composite roll |
| JPH03122249A (en) * | 1989-10-06 | 1991-05-24 | Kawasaki Steel Corp | Centrifugally cast high chromium roll |
| JPH03254354A (en) * | 1990-03-05 | 1991-11-13 | Fujikoo:Kk | Manufacture of looper roller in hot rolling mill |
| JPH05271855A (en) * | 1992-03-23 | 1993-10-19 | Hitachi Metals Ltd | Roll material for hot strip rolling |
Cited By (10)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| EP0911421A4 (en) * | 1997-04-08 | 2000-05-31 | Nippon Steel Corp | COMPOSITE ROLLER FOR COLD ROLLING |
| US6206814B1 (en) | 1997-04-08 | 2001-03-27 | Nippon Steel Corporation | Composite work roll for cold rolling |
| CN102002644A (en) * | 2010-09-26 | 2011-04-06 | 中钢集团邢台机械轧辊有限公司 | Working roll for automobile sheet cold rolling and manufacturing method thereof |
| CN103008617A (en) * | 2012-12-27 | 2013-04-03 | 江西省科学院应用物理研究所 | Method for preparing high-speed steel composite roll for hot rolling |
| CN103008617B (en) * | 2012-12-27 | 2014-09-10 | 江西省科学院应用物理研究所 | Method for preparing high-speed steel composite roll for hot rolling |
| CN107891138A (en) * | 2017-11-09 | 2018-04-10 | 常州凯达重工科技有限公司 | A kind of preparation technology for being used to make the super high-vanadium high-speed steel pressure roller of corrugated metal sheet |
| JP2020063485A (en) * | 2018-10-17 | 2020-04-23 | Jfeスチール株式会社 | Work roll for hot-rolling rough stand |
| CN111036873A (en) * | 2020-01-20 | 2020-04-21 | 青岛鑫盛源轧辊有限公司 | Centrifugal composite ductile iron cast steel roll and preparation method thereof |
| CN111036873B (en) * | 2020-01-20 | 2021-06-08 | 青岛鑫盛源轧辊有限公司 | Centrifugal composite ductile iron cast steel roll and preparation method thereof |
| CN117187601A (en) * | 2022-05-31 | 2023-12-08 | 天津重型装备工程研究有限公司 | Supporting roller of medium-broadband rolling mill and centrifugal composite casting method |
Also Published As
| Publication number | Publication date |
|---|---|
| JP3006984B2 (en) | 2000-02-07 |
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