JPS58133353A - Casing for steam turbine - Google Patents

Casing for steam turbine

Info

Publication number
JPS58133353A
JPS58133353A JP1493982A JP1493982A JPS58133353A JP S58133353 A JPS58133353 A JP S58133353A JP 1493982 A JP1493982 A JP 1493982A JP 1493982 A JP1493982 A JP 1493982A JP S58133353 A JPS58133353 A JP S58133353A
Authority
JP
Japan
Prior art keywords
less
casing
cast steel
steam turbine
cracking
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
Application number
JP1493982A
Other languages
Japanese (ja)
Other versions
JPS6123260B2 (en
Inventor
Takatoshi Yoshioka
吉岡 孝利
Seishin Kirihara
桐原 誠信
Masao Shiga
志賀 正男
Takehiko Yoshida
武彦 吉田
Shigeki Saito
茂樹 斉藤
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.)
Hitachi Ltd
Original Assignee
Hitachi Ltd
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 Hitachi Ltd filed Critical Hitachi Ltd
Priority to JP1493982A priority Critical patent/JPS58133353A/en
Publication of JPS58133353A publication Critical patent/JPS58133353A/en
Publication of JPS6123260B2 publication Critical patent/JPS6123260B2/ja
Granted legal-status Critical Current

Links

Landscapes

  • Heat Treatment Of Articles (AREA)

Abstract

PURPOSE:To provide the titled casing high in creep breaking strength and low SR crack sensitivity, containing C, Mn, Si, Cr, Mo, V, Ni, B and a nitride forming element having nitride forming ability higher than that B respectively in a predetermined ratio and comprising cast steel having bainite structure mainly. CONSTITUTION:The titled casing comprises a cast steel material containing, on the basis of wt%, 0.05-0.2% C, 2% or less Mn, 1% or less Si, 0.5-2% Cr, 0.5- 2% Mo, 0.05-0.5% V, 0.5% or less Ni, 0.0002-0.005% B and 0.1% or less nitride forming element alone or 0.2% or less in composite and comprising the remainder Fe. This nitride forming element has nitride forming ability larger than that of B and this cast steel has a bainite structure mainly. The titled casing comprising this cast steel has high creep breaking strength at 550-650 deg.C and shows excellent characteristics low in SR crack sensitivity during a welding process.

Description

【発明の詳細な説明】 本発明は新規な蒸気タービン用ケーシングに係9、特に
550〜60(1’にさらされる高効4c蒸気タービン
のケーシング本体、主蒸気弁ケーシング及び加減弁ケー
シングに高いクリープ破断強度と8R割れ感受性が低い
すぐれた特性を示すCr−MO−V鋳鋼を使用しえ蒸気
タービン用ケークングに関する。
DETAILED DESCRIPTION OF THE INVENTION The present invention relates to a novel casing for steam turbines, particularly 550-60 (1' This invention relates to a caking for a steam turbine using Cr-MO-V cast steel which exhibits excellent properties such as low breaking strength and low susceptibility to 8R cracking.

従来の蒸気タービンは蒸気温度最大566C。Conventional steam turbines have a maximum steam temperature of 566C.

蒸気圧力最大246 atgであり、第1図に示すケー
シング本体l及び加減弁ケーシング2、及び第2図に示
す主蒸気弁ケーシング材としてはCr−MO−V鋳鋼が
用いられている。
The maximum steam pressure is 246 atg, and Cr-MO-V cast steel is used for the casing body 1 and regulating valve casing 2 shown in FIG. 1, and the main steam valve casing material shown in FIG. 2.

最近、石油9石炭などの化石燃料のコストが上昇を続け
ておplごれら化石燃料を用いている火力プラントの発
電効率が重要になっている0発電効率を上げるためには
蒸気タービンの蒸気温度又は圧力を上げる必要がある。
Recently, as the cost of fossil fuels such as petroleum 9 and coal continues to rise, the power generation efficiency of thermal power plants that use fossil fuels has become important. It is necessary to increase the temperature or pressure.

これら高効率タービン用材料としては、現用タービン材
では強度不足で、これよ如も高強度の材料が必要である
As materials for these high-efficiency turbines, currently used turbine materials lack strength, so materials with even higher strength are needed.

発明者らは、上述ケーシング材としてCr−MO−V鋳
鋼を基本組成とし、微量のボロンを添加したボロン入b
cr−MO−vs鋼の適用を検討した。しかし、ボロン
は、その含有量の増加によって焼入れ性を増し、貢温強
度を高める反面、溶接性を低め、更に8R割れ感受性を
著しく高めることを究明した。したがって、補修#*や
継手溶接が行われるケーシング材へのボロン添加に対し
、強度を向上させ、さらに溶接性を向上させ、88割れ
を防止する必要があつ九。
The inventors used boron-containing b, which has a basic composition of Cr-MO-V cast steel and added a small amount of boron, as the above-mentioned casing material.
The application of cr-MO-vs steel was studied. However, it has been found that increasing boron content increases hardenability and temperature-induced strength, but at the same time reduces weldability and significantly increases 8R cracking susceptibility. Therefore, it is necessary to improve the strength, further improve weldability, and prevent 88 cracks by adding boron to the casing material used for repair #* and joint welding.

本発明の目的は、550〜600t:’において高いク
リープ破断強度を有し、又#l接工程における耐8B割
れ感受性の低い極めて良好な鋳鋼からなる蒸気タービン
用ケーシングを提供するにある。
An object of the present invention is to provide a steam turbine casing made of extremely good cast steel that has high creep rupture strength at 550 to 600 t:' and low susceptibility to 8B cracking in the #l welding process.

下、Sム1%以下、Crα5〜2%、MOα5〜2%。Bottom, SM 1% or less, Crα 5-2%, MOα 5-2%.

Vo、05〜0.5%、Niα5%以下、 BQ、00
02〜0.005%と、Bよシ窒化物形成能カが大きい
窒化物形成元素が単独でα1%以下又は複合で0.2%
以下とを含み、残部は実質的KFeからなシ、主にベー
ナイト組織を有する鋼からなることを特徴とする蒸気タ
ービン用ケーシングにある。
Vo, 05~0.5%, Niα5% or less, BQ, 00
02 to 0.005%, and the nitride-forming elements, which have higher nitride-forming ability than B, are α1% or less alone or 0.2% in combination.
The casing for a steam turbine is characterized in that it includes the following, the remainder being substantially KFe-free and mainly made of steel having a bainitic structure.

更に、本発明は前述(DC,S i、 Mfl、 Cr
、 Ni。
Furthermore, the present invention has the above-mentioned (DC, Si, Mfl, Cr
, Ni.

V、B及び命化物形成元素を含有するcr−MO−V系
低合金鋳鋼に、Mnよシ硫化物形成能カが大きい硫化物
形成元素をα0002〜α2%含むものである。
The cr-MO-V-based low alloy cast steel containing V, B, and life-forming elements contains α0002 to α2% of sulfide-forming elements that have a higher sulfide-forming ability than Mn.

本発明により、溶接工程における88割れ感受性を著し
く低下せしめ、しかも高温強度が高められることを実験
的に究明した。
It has been experimentally determined that the present invention significantly reduces susceptibility to 88 cracking in the welding process and increases high-temperature strength.

前記窒化物形成元素はAt、 Ti、 Nb及び7.r
の1種以上が好ましい、前記硫化物形成元素はCa及び
Mgの少なくとも1つが好・ましい。
The nitride-forming elements include At, Ti, Nb and 7. r
The sulfide-forming element is preferably at least one of Ca and Mg.

Cはα05%以上において、クリープ破断強度を得るた
めに必要な元素であるが、その量が0.2%を越えると
、高温に長時間さらされた場合に組織が不安定になp長
時間クリープ破断強度を低下させ、更に溶接工程におけ
る溶接部の割れ感受性を高めるので、O,OS〜α2%
 にしなければならない0%に、0.1〜0.15%が
好ましい。
C is an element necessary to obtain creep rupture strength at α05% or more, but if its amount exceeds 0.2%, the structure becomes unstable when exposed to high temperatures for a long time. Since it reduces the creep rupture strength and further increases the cracking susceptibility of the welded part during the welding process, O,OS~α2%
It should be 0%, preferably 0.1-0.15%.

Bt及びMnは脱酸剤として添加するものであシ、少量
の添加で十分効果は達成される。S轟及びRJIは焼入
性を増加させる元素であるが、反面多量添加によって焼
もどし脆化感受性を高める。
Bt and Mn are added as deoxidizing agents, and sufficient effects can be achieved by adding a small amount. S Todoroki and RJI are elements that increase hardenability, but on the other hand, when added in large amounts, they increase the susceptibility to tempering embrittlement.

そのため、夫々S1は1%及びMl)は2%以下としな
ければならない。特に、Siは0.2〜0.6%及びM
nは0.6〜1.0%が好ましい。
Therefore, S1 must be 1% and Ml) must be 2% or less, respectively. In particular, Si is 0.2-0.6% and M
n is preferably 0.6 to 1.0%.

N1は靭性を高めるのに非常に有効である反面、α5%
を越える添加は、クリープ破断強度を低下させるので、
α5%以下でなければならない。特に、α05〜0.3
%が好ましい。
While N1 is very effective in increasing toughness, α5%
Addition of more than
α must be less than 5%. In particular, α05~0.3
% is preferred.

Crは高温強度及び耐酸性を高めるものであシ、高温材
料として欠くことのできない元素である。
Cr increases high-temperature strength and acid resistance, and is an indispensable element for high-temperature materials.

そのためには(15%以上は必要であるが、2%を越え
ると析出炭化物の粗大化が生じ、クリープ破断強度が低
下するので、Cr含有量は0.5〜2%の範囲であるこ
とが必要である。特に、α9〜1.5%が好ましい。
To achieve this, the Cr content must be 15% or more, but if it exceeds 2%, the precipitated carbides will become coarser and the creep rupture strength will decrease, so the Cr content should be in the range of 0.5 to 2%. It is necessary. In particular, α9 to 1.5% is preferable.

MOは固溶強化及び析出硬化作用によってクリープ強度
を改善し、更に焼もどし脆化を防止する元素であるが、
0.5%未満ではその効果は不十分であり、2%を越え
てもそれ以上の効果がなく飽和する。し九がってMOは
α5〜2%の範囲が有効である。特に、α9〜1.5%
が最も有効である。
MO is an element that improves creep strength through solid solution strengthening and precipitation hardening effects, and also prevents tempering embrittlement.
If it is less than 0.5%, the effect is insufficient, and if it exceeds 2%, there is no further effect and the effect is saturated. Therefore, it is effective for MO to have α in the range of 5 to 2%. Especially α9~1.5%
is the most effective.

■は炭素と結合して、炭化物を形成し、クリープ破断強
度を高める。しかし、0.05%未満ではその効果は不
十分でTo#)、逆に、α5%を越えると溶接工程にお
ける88割れ感受性を高めると共に、クリープ破断延性
を低下させるので、O,OS〜α5%の範囲でなければ
ならない。特に、0.1〜0.35%が蛾も有効である
(2) combines with carbon to form carbide and increase creep rupture strength. However, if the content is less than 0.05%, the effect is insufficient (To must be within the range. In particular, 0.1 to 0.35% of moths is also effective.

Bは焼入性を向上させ、クリープ破断強度を高める。し
かし、その効果は0.0001%未満では不十分であシ
、α005%を越えると溶接性、籍にSR割れ感受性を
高める。したがって、00001〜α005%の範囲に
しなければならない。特に、α0008〜α003%が
最も有効である。
B improves hardenability and increases creep rupture strength. However, the effect is insufficient if it is less than 0.0001%, and if it exceeds α005%, weldability and susceptibility to SR cracking will increase. Therefore, it must be in the range of 00001 to α005%. In particular, α0008 to α003% is the most effective.

Bより窒化物形成能力が大きい窒化物形成元素はNの固
定を目的として添加するものである。NはBと結合し、
B本来の効果を減する。そのためBよシ窒化物形成能力
の大きい元素をBとともに複合添加させ、Nを固定化さ
せてB本来の効果を発揮させる必要がある。この効果は
、単独で、0.1%又は複合で0.2%を越えると逆に
クリープ破断延性を著しく低下させる。この元素として
、kt。
A nitride-forming element having a higher nitride-forming ability than B is added for the purpose of fixing N. N combines with B,
B Reduce the original effect. Therefore, it is necessary to add an element having a greater ability to form nitrides than B in combination with B, to fix N and to exert the original effect of B. When this effect exceeds 0.1% alone or 0.2% in combination, the creep rupture ductility is significantly reduced. As this element, kt.

’l’1.Nb及び7.rが最も好ましい。これらの元
素は複合添加の方が効果が大きい。At0.01〜0.
05%。
'l'1. Nb and 7. r is most preferred. Addition of these elements in combination is more effective. At0.01~0.
05%.

TiO,01〜0.08%、NbO,01〜α08%及
びzro、01〜0.08%が最も有効である。
TiO, 01-0.08%, NbO, 01-08%, and zro, 01-0.08% are the most effective.

Mnよシ硫化物形成能力よシ大きい硫化物形成元素の0
.0002%以上の添加は、製鋼中における脱硫及び脱
Pとして作用させるとともに、鋼中の8を固定し、溶接
熱影響部の結晶粒界へのSの偏析を抑制し、SR割れを
防止するものである。
0 of the sulfide-forming elements, which has a greater sulfide-forming ability than Mn.
.. Addition of 0002% or more acts as desulfurization and dephosphorization during steelmaking, fixes 8 in the steel, suppresses segregation of S to the grain boundaries of the weld heat affected zone, and prevents SR cracking. It is.

SR割れは溶接熱影響部の結晶粒界の割れでめシ、S−
?Pなどの不純吻元素のうち、特にSが結晶粒界への偏
析が多いほど発生し易い、しかし、062%を越える添
加は耐SR割れ性に対するそれ以上の効果がない、Mn
より硫化物形成能力の大きい元素として、Ca及びMg
が有効である。これらの元素は溶接熱影響部の結晶粒界
のSa度が減少し、耐S′fL割れ感受性を向上させる
。特に本発明においてはBを添加してクリープ領置を高
めているが、B#加によって逆にSR割れ発生の恐れが
ある。
SR cracking is a crack at grain boundaries in the heat affected zone of welding, and S-
? Among impurity elements such as P, S in particular is more likely to occur as it segregates to grain boundaries. However, addition of more than 0.62% has no further effect on SR cracking resistance.
Ca and Mg are elements with greater sulfide forming ability.
is valid. These elements reduce the Sa degree of the grain boundaries in the weld heat affected zone and improve the S'fL cracking resistance. In particular, in the present invention, B is added to increase the creep retention, but the addition of B# may actually cause SR cracking.

したがってCal添加はSR割れ防止の点で必費元索で
ある。添加量は0.0002%以下では耐SR割れ性に
効果がな(,0,2%以上ではその効果が飽和する。適
量としてはα005〜0.05%が有効である。
Therefore, addition of Cal is a necessary cost in terms of preventing SR cracking. If the amount added is less than 0.0002%, it has no effect on SR cracking resistance (and if it is more than 0.2%, the effect is saturated. As an appropriate amount, α005 to 0.05% is effective.

本発明の蒸気タービン用ケーシングは、主にベーナイト
組織を有するものでなければならない。
The steam turbine casing of the present invention must primarily have a bainitic structure.

ベーナイト組織は焼戻しベーナイト組織が好ましく、高
温において高強度を有する。化学組成及び熱処理によっ
てはフェライト組織が生じるので、実質的にフェライト
組織が析出しないように全ベーナイト組織とすることが
最も有効である。
The bainite structure is preferably a tempered bainite structure, which has high strength at high temperatures. Since a ferrite structure may occur depending on the chemical composition and heat treatment, it is most effective to form the entire bainite structure so that the ferrite structure does not substantially precipitate.

実施例 高周波鰐導溶解炉を用いて鋳鋼塊を作製した。Example A cast steel ingot was produced using a high-frequency Wani induction melting furnace.

第1表はそれら代表的試料の化学組成を示す。Table 1 shows the chemical composition of these representative samples.

いずれ+7)鋼jJL41,050C,15時間堡持後
、400C/hの焼ならし処理を施し、その後A1には
710tl’、15時間保持及び162,3.4には7
20C,15時間保持後炉冷の焼もどし#&壜をそれぞ
れ施した。
+7) Steel jJL41,050C, after 15 hours of normalization treatment at 400C/h, then 710 tl' for A1, held for 15 hours, and 7 for 162, 3.4.
After holding at 20C for 15 hours, furnace-cooling tempering #&bottle was performed, respectively.

試料はICr−IMO−1/4V、At、Tム、B及び
C−量を変化させ九、A1はB及びcao無添加材の比
較材である。42はBを0.0015%添加し、Ca無
添加材、&3及び4はB及びca添加の本発明材である
The samples were ICr-IMO-1/4V, with varying amounts of At, T, B, and C. A1 is a comparative material without B and cao additives. No. 42 is a material with 0.0015% B added and no Ca added, and &3 and 4 are materials of the present invention with B and ca added.

いずれの試料も全ベーナイト組織であった。All samples had an entirely bainite structure.

SR割れ感受性試験はJIS  Z3158に準じ、試
料を斜めY形溶接割れ試験片(板厚3o■)に加工して
行った。溶接は市販のOr−Mo鋼用被覆アークS*棒
(4φ)を用い、第2表の条件で行った。
The SR cracking susceptibility test was carried out in accordance with JIS Z3158 by processing the sample into a diagonal Y-shaped weld cracking test piece (plate thickness: 3°). Welding was performed using a commercially available coated arc S* rod (4φ) for Or-Mo steel under the conditions shown in Table 2.

第3表は各種機械試験結果を示す。Table 3 shows the results of various mechanical tests.

B添加材は無添加材に比べて、衝撃特性はわずか低下す
るものの、引張強度は著しく高い。
Although the B-additive material has slightly lower impact properties than the non-additive material, the tensile strength is significantly higher.

一方、600C,10’時間クリープ破断強度が本発明
材では9.9〜10.2Kt/■8で、高効率蒸気ター
ビン用ケーシング材としてきわめて顕著な効果を有し、
比較材41よシも著しく高いことが確認された。
On the other hand, the material of the present invention has a 600C, 10' hour creep rupture strength of 9.9 to 10.2Kt/■8, which is extremely effective as a casing material for high-efficiency steam turbines.
It was confirmed that comparative material 41 was also significantly higher.

第3図はSR割れ試験結果を示すグラフである。FIG. 3 is a graph showing the results of the SR cracking test.

本発明と比較材において、B及びclをふ加しないAl
材はSR割れは発生しないが、Bを0.0015%添加
のA2において、sFL割れ率61%のSR割れが発生
し友。それはB添加によってSR割れが助長されること
を示している。一方、I62に対して、Btが同じでC
Iを添加した本発明の43においてはSR割れは発生し
ない。更KB量が0.002%まで増加し、caを添加
した本発明の14においてもSR割れは発生しなかった
。以上の結果、本発明はSR割れ感受性が極めて低いこ
とが明らかである。
In the present invention and comparative materials, Al without adding B and Cl
Although SR cracking did not occur in the material, SR cracking occurred in A2 with 0.0015% B addition, with an sFL cracking rate of 61%. This indicates that the addition of B promotes SR cracking. On the other hand, for I62, Bt is the same and C
In No. 43 of the present invention in which I was added, SR cracking did not occur. Furthermore, SR cracking did not occur in Sample No. 14 of the present invention in which the KB amount was increased to 0.002% and Ca was added. From the above results, it is clear that the present invention has extremely low susceptibility to SR cracking.

以上、本発明鋼は高温強度及び靭性が高く、更に耐SR
割れ感受性が極めて良好であり、特に、600Cまでの
高温クリープ破断強度は著しく高く、高効率蒸気タービ
ン用ケーシングとして要求される強度を十分満足してい
ることが明らかであシ、550〜600Cでの高効率蒸
気タービン用ケーシングとして好適であシ、本発明が及
ぼす産業への発達に寄与する効果は極めて大きい。
As mentioned above, the steel of the present invention has high high temperature strength and toughness, and also has high SR resistance.
It has extremely good cracking susceptibility, and in particular, the high-temperature creep rupture strength up to 600C is extremely high, clearly satisfying the strength required for high-efficiency steam turbine casings. It is suitable as a casing for a high-efficiency steam turbine, and the effect of the present invention contributing to the development of industry is extremely large.

【図面の簡単な説明】 第1図は蒸気タービン用ケーシング本体、蒸気加減弁ケ
ーシングの断面構成図、第2図は主蒸気弁ケーシングの
断面構成図及び第3図は溶接後のSR処理による割れ率
を示すグラフである。 1・・・ケーシング本体、2・・・加減弁ケーシング、
3第7 図
[Brief explanation of the drawings] Figure 1 is a cross-sectional diagram of the steam turbine casing body and steam control valve casing, Figure 2 is a cross-sectional diagram of the main steam valve casing, and Figure 3 shows cracks caused by SR treatment after welding. It is a graph showing the rate. 1...Casing body, 2...Adjustment valve casing,
3Figure 7

Claims (1)

【特許請求の範囲】 1、重量で、C0,05〜0.2%、Mn2%以下、 
 811%以下、 Cr (L5〜2%、 Mo 0.
5〜2%、 vo、os〜0.5%、N1CL5%以下
、 B O,0001〜a00 烏と、該Bよp会化物
形成能力が大きい窒化物形成元素が単独で0.1%以下
又は複合で0.2%′以下とを含み、残部は実質的にp
eからなシ、主にベーナイト組織を有する鋳鋼からなる
ことを特徴とする蒸気タービン用ケーシング。 2、前記窒化物形成元素がht、l、Nb及び7、rで
ある特許請求の範囲第1項に記載の蒸気タービン用ケー
シング。 3、重量で、Cα05〜0.2%、Mn2%以下、81
1%以下、cro、s〜2%、MOo、5〜2%、vo
、os〜α5%、NiO,5%以下と、80.0002
〜0.005%と、鋏Bよシ窒化物形成能力が大きい窒
化物形成元素が単独でa1%以下又は複合で0.2%以
下と、前記Mr1よ)硫化物形成能力が大きい硫化物形
成元素0.0002〜α2%とを含み、残部は実質的に
peからなシ、主にベーナイト組織を有する鋳鋼からな
ることを4!徴とする蒸気タービン用ケーシング。 4、前記硫化物形成元素がCI及びMgの少なくとも1
種である特許請求の範囲第3項に記載の蒸気タービン用
ケーシング。
[Claims] 1. By weight, C0.05 to 0.2%, Mn 2% or less,
811% or less, Cr (L5~2%, Mo 0.
5 to 2%, vo, os to 0.5%, N1CL 5% or less, B O,0001 to a00 and the nitride-forming element that has a large p-type oxide forming ability as B alone is 0.1% or less, or The composite contains 0.2% or less, and the remainder is substantially p.
A casing for a steam turbine, characterized in that it is made of cast steel having mainly a bainitic structure. 2. The steam turbine casing according to claim 1, wherein the nitride-forming elements are ht, l, Nb, and 7, r. 3. By weight, Cα05-0.2%, Mn 2% or less, 81
1% or less, cro, s~2%, MOo, 5~2%, vo
, os~α5%, NiO, 5% or less, and 80.0002
~0.005%, and scissors B has a large nitride-forming ability.The nitride-forming element alone is 1% or less, or in combination is 0.2% or less, and the above-mentioned Mr1) has a large sulfide-forming ability. 4! Contains 0.0002 to α2% of elements, and the remainder is essentially composed of cast steel with a bainitic structure. A steam turbine casing with a distinctive feature. 4. The sulfide forming element is at least one of CI and Mg.
The casing for a steam turbine according to claim 3, which is a seed.
JP1493982A 1982-02-03 1982-02-03 Casing for steam turbine Granted JPS58133353A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP1493982A JPS58133353A (en) 1982-02-03 1982-02-03 Casing for steam turbine

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP1493982A JPS58133353A (en) 1982-02-03 1982-02-03 Casing for steam turbine

Publications (2)

Publication Number Publication Date
JPS58133353A true JPS58133353A (en) 1983-08-09
JPS6123260B2 JPS6123260B2 (en) 1986-06-05

Family

ID=11874924

Family Applications (1)

Application Number Title Priority Date Filing Date
JP1493982A Granted JPS58133353A (en) 1982-02-03 1982-02-03 Casing for steam turbine

Country Status (1)

Country Link
JP (1) JPS58133353A (en)

Cited By (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JP2007197774A (en) * 2006-01-26 2007-08-09 Toshiba Corp Heat-resistant cast steel
JP2011001943A (en) * 2009-06-22 2011-01-06 Hitachi Ltd Steam turbine casing
WO2015163226A1 (en) * 2014-04-23 2015-10-29 日本鋳鍛鋼株式会社 Turbine rotor material for geothermal power generation and method for manufacturing same

Cited By (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JP2007197774A (en) * 2006-01-26 2007-08-09 Toshiba Corp Heat-resistant cast steel
JP2011001943A (en) * 2009-06-22 2011-01-06 Hitachi Ltd Steam turbine casing
WO2015163226A1 (en) * 2014-04-23 2015-10-29 日本鋳鍛鋼株式会社 Turbine rotor material for geothermal power generation and method for manufacturing same
JP5869739B1 (en) * 2014-04-23 2016-02-24 日本鋳鍛鋼株式会社 Turbine rotor material for geothermal power generation and method for manufacturing the same

Also Published As

Publication number Publication date
JPS6123260B2 (en) 1986-06-05

Similar Documents

Publication Publication Date Title
CA1066922A (en) Heat-resistant allow for welded structures
JPS58125396A (en) Austenitic welded structure
EP0492674A1 (en) Ferritic heat-resisting cast steel and a process for making the same
JPH0114305B2 (en)
CN111394663A (en) Heat-resistant iron-based alloy and preparation method thereof
US4381940A (en) Low alloy heat-resisting steel for high temperature use
JPS6253583B2 (en)
JPS6344814B2 (en)
JPS6250542B2 (en)
JPH06322488A (en) High-strength austenitic heat resistant steel excellent in weldability and satisfactory in high temperature corrosion resistance
JPS58133353A (en) Casing for steam turbine
JP5011622B2 (en) Stainless cast steel with excellent heat resistance and machinability
JPS6123749A (en) Austenitic stainless steel having high strength at high temperature
JP2831051B2 (en) Austenitic stainless steel welding wire
JPS6249344B2 (en)
JPS59136464A (en) Boiler tube
JPS58110662A (en) Heat resistant steel
JPH11229059A (en) Heat resistant alloy for engine valve
JPH10225792A (en) Tig welding material for austenitic heat resistant steel excellent in high temperature strength
US5753179A (en) Steels for exhaust valves having improved fatigue strength at high temperature, corrosion resistance at room and higher temperatures and oxidation resistance
JPS60152647A (en) Nickel alloy
US3839025A (en) High temperature alloy
JPH0553859B2 (en)
JP2002001579A (en) WELDING WIRE FOR LOW-Cr-CONTENT, HIGH-STRENGTH, HIGH- TOUGHNESS HEAT-RESISTING STEEL
CA1053937A (en) High temperature cast austenitic exhaust valve