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JPS58500B2 - Tainetsugoukin - Google Patents
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JPS58500B2 - Tainetsugoukin - Google Patents

Tainetsugoukin

Info

Publication number
JPS58500B2
JPS58500B2 JP1020375A JP1020375A JPS58500B2 JP S58500 B2 JPS58500 B2 JP S58500B2 JP 1020375 A JP1020375 A JP 1020375A JP 1020375 A JP1020375 A JP 1020375A JP S58500 B2 JPS58500 B2 JP S58500B2
Authority
JP
Japan
Prior art keywords
strength
heat
present
added
alloys
Prior art date
Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
Expired
Application number
JP1020375A
Other languages
Japanese (ja)
Other versions
JPS5184722A (en
Inventor
行俊照夫
椹木義淳
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
Nippon Steel Corp
Original Assignee
Sumitomo Metal Industries 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 Sumitomo Metal Industries Ltd filed Critical Sumitomo Metal Industries Ltd
Priority to JP1020375A priority Critical patent/JPS58500B2/en
Publication of JPS5184722A publication Critical patent/JPS5184722A/en
Publication of JPS58500B2 publication Critical patent/JPS58500B2/en
Expired legal-status Critical Current

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  • Heat Treatment Of Nonferrous Metals Or Alloys (AREA)

Description

【発明の詳細な説明】 本発明は高温強度の優れた耐熱合金に関するものである
DETAILED DESCRIPTION OF THE INVENTION The present invention relates to a heat-resistant alloy with excellent high-temperature strength.

従来化学工業用、特にエチレンプラントの分解炉や改質
炉にはHK40(0,4C−25Cr−2ONi)など
の遠心鋳造管が使用されているが鋳造合金では小径薄肉
の管の製造が不可能であるばかりでなく、製品の長さが
限定されるため強度的に不安定な溶接部が増加する欠点
がある。
Conventionally, centrifugally cast tubes such as HK40 (0,4C-25Cr-2ONi) have been used in the chemical industry, especially in cracking furnaces and reforming furnaces in ethylene plants, but it is impossible to manufacture small-diameter, thin-walled tubes with cast alloys. Moreover, since the length of the product is limited, there is a drawback that the number of welded parts that are unstable in strength increases.

更に化学工業に於ては効率化のため高温化が益益必要と
なるが、化学工業用鍛伸管として現在実用化されている
インコロイ800(20Cr−3ONi−Ti−At)
では高温強度が必ずしも充分でなく、化学工業用の安定
化操業と能率化のためには高温強度が高く、しかも細径
長尺管の製造可能な鍛伸材の開発が強く要望されている
Furthermore, in the chemical industry, higher temperatures are necessary for efficiency, and Incoloy 800 (20Cr-3ONi-Ti-At), which is currently in practical use as a forged and drawn pipe for the chemical industry,
However, in order to stabilize operations and improve efficiency in the chemical industry, there is a strong demand for the development of a forged material that has high temperature strength and can be used to produce long, narrow-diameter tubes.

本発明は上記の要望に答えるために、本発明者等が鋭意
研究した結果完成したもので、従来の鍛造合金よりも高
温強度に優れだ固溶強化型鍛造耐熱合金を提供するにあ
る。
The present invention was completed as a result of intensive research by the present inventors in order to meet the above-mentioned needs, and its purpose is to provide a solid solution strengthened forged heat-resistant alloy that has superior high-temperature strength than conventional forged alloys.

即ち本発明の要旨とするところはC,0,01〜0.3
%、SiO,01〜1.0%、MnX0.01〜2.0
%、Cr、10〜30%、M2.0.003〜0.05
%及びMo13〜25%、W、3〜25%の何れか一方
又は両方(但し、MoとWの両方を含む場合にはNoと
Wの合計で3〜25%。
That is, the gist of the present invention is that C, 0.01 to 0.3
%, SiO, 01-1.0%, MnX 0.01-2.0
%, Cr, 10-30%, M2.0.003-0.05
%, Mo13-25%, W, 3-25%, or both (however, if both Mo and W are included, the total of No and W is 3-25%.

)を含有し残部はNi(但し、Ni、10%以下をFe
と置換できる。
) and the remainder is Ni (however, Ni, 10% or less is Fe).
can be replaced with

)と不可避的不純物とよりなるオーステナイト耐熱合金
か、又は上記成分に更にB、0.001〜0.05%、
Zr10.001〜1.0係の何れか一方又は両方を含
有するオーステナイトi熱合金よりなり、Cが固溶した
オーステナイト組織を有する高温強度の大なる耐熱合金
である。
) and unavoidable impurities, or the above components further include B, 0.001 to 0.05%,
It is an austenitic i-thermal alloy containing one or both of Zr 10.001 to 1.0, and has an austenitic structure in which C is dissolved as a solid solution, and has high high-temperature strength.

本発明に於てCが固溶したオーステナイト組織とするに
は情態化処理が必要であり、溶体化処理温度が1200
℃以下ではCの固溶化が充分でないだめ得られた耐熱合
金は耐熱性の満足なものが得られないし、又処理時間が
1分取分てはCの固溶化が充分促進されない。
In the present invention, in order to form an austenitic structure in which C is dissolved as a solid solution, a solution treatment is necessary, and the solution treatment temperature is 1200
If the temperature is below .degree. C., the resulting heat-resistant alloy will not have satisfactory heat resistance unless C is sufficiently dissolved into a solid solution, and even if the treatment time is 1 minute, the solution of C will not be sufficiently promoted.

次に本発明の成分を限定した理由を下記に詳細説明する
Next, the reason for limiting the components of the present invention will be explained in detail below.

Cは耐熱合金として必要な引張強さ及びクリープ破断強
度など耐熱特性を向上させるのに有効な成分で、0.0
1%以上必要であるが、0.30%を越えると熱処理状
態で固溶残りのCが増加して高温強度が低下する。
C is an effective component for improving heat-resistant properties such as tensile strength and creep rupture strength required for a heat-resistant alloy, and is 0.0
1% or more is required, but if it exceeds 0.30%, the amount of C remaining in solid solution increases during heat treatment, resulting in a decrease in high-temperature strength.

Siは溶鋼の脱酸剤として必要であるが、成分組成が1
.0%を越えると溶接性の劣化を来し、0.01%未満
では強度低下をもたらすためその範囲として0.01〜
1.0%とした。
Si is necessary as a deoxidizing agent for molten steel, but its composition is 1.
.. If it exceeds 0%, weldability will deteriorate, and if it is less than 0.01%, it will cause a decrease in strength, so the range is from 0.01 to
It was set as 1.0%.

Mnは脱酸材、加工性改善のため添加するものであるが
、過剰添加すると耐熱特性を劣化させる故、0.01〜
2%とした。
Mn is added as a deoxidizing agent and to improve processability, but excessive addition deteriorates heat resistance properties, so it should be added in the range of 0.01 to
It was set at 2%.

Crは耐酸化性、靭性の改善に優れた効果を示すが、1
0%未満では耐酸化性が劣り、30%を越えると安定し
た完全オーステナイト相を得ることが困難である。
Cr shows excellent effects on improving oxidation resistance and toughness, but 1
If it is less than 0%, oxidation resistance is poor, and if it exceeds 30%, it is difficult to obtain a stable complete austenite phase.

Mgは0.003 %以上の添加により加工性の向上に
効果を示すが、0.05%を越えると加工性及び溶接性
が低下する。
Mg is effective in improving workability when added in an amount of 0.003% or more, but if it exceeds 0.05%, workability and weldability decrease.

Mo及びWは共に主として固溶強化として高温強度向上
に有効であるが、過剰に添加すると加工性が悪くなり、
合金の組織を不安定化して脆化相を析出させ、少なすぎ
ると固溶強化が充分発揮できないのでMoとWの単独添
加の場合には夫々3〜25%、MoとWとを両方添加し
た場合にM。
Both Mo and W are effective in improving high-temperature strength mainly as solid solution strengthening, but when added in excess, workability deteriorates.
It destabilizes the structure of the alloy and precipitates a brittle phase, and if it is too small, solid solution strengthening cannot be achieved sufficiently, so when adding Mo and W alone, 3 to 25% each was added, and both Mo and W were added. M in case.

とWの合計で同様に3〜25%の範囲に限定する必要が
ある。
It is necessary to similarly limit the total amount of W and W to a range of 3 to 25%.

Feは経済的な面を考慮してNiの一部と置き換えるこ
とが可能であるが過度に添加すると脆化相を析出する故
にNiと置換し得るFeの量を10%以下とした。
Considering the economic aspect, Fe can be partially replaced with Ni, but if excessively added, a brittle phase will precipitate, so the amount of Fe that can be replaced with Ni was set to 10% or less.

Bはオーステナイト耐熱合金0.001%以上含有させ
ると高温強度の改善に有効であるが、0.05%を越え
ると熱間加工性及び溶接性が劣化する。
If 0.001% or more of B is contained in the austenitic heat-resistant alloy, it is effective in improving high-temperature strength, but if it exceeds 0.05%, hot workability and weldability deteriorate.

ZrはBと同様にo、ooi%以上の添加により耐熱特
性を向上させるが、過剰になると粗大な炭化物を形成し
て強度低下をもたらす故0.001〜1.0%を限度と
する。
Like B, Zr improves heat resistance when added in an amount of o, ooi% or more, but if it is excessive, coarse carbides are formed and strength is reduced, so the limit is 0.001 to 1.0%.

次に本発明を実施例によって詳細説明する。Next, the present invention will be explained in detail by way of examples.

実施例 1 本発明及び本発明の合金組成に属さない従来の合金を比
較例として夫々1000℃に於けるクリープ破断強度及
び1000℃に於ける短時間引張り特注について試験を
行った。
Example 1 The present invention and a conventional alloy that does not belong to the alloy composition of the present invention were tested for creep rupture strength at 1000°C and short-time tensile strength at 1000°C as comparative examples.

本発明の場合、溶体化処理条件を温度1250℃時間を
15分間としれ 比較としてインコロイ800、インコネル625を使用
し丸共にインターナショナル、ニッケル、カンパニー(
InternationalNickelCompan
y)製で前者はFe−Cr −Ni系合金、後者はNi
−Cr系合金である。
In the case of the present invention, the solution treatment conditions were a temperature of 1250°C for 15 minutes, Incoloy 800 and Inconel 625 were used for comparison.
InternationalNickelCompan
y), the former is Fe-Cr-Ni alloy, the latter is Ni
-Cr-based alloy.

これらの成分組成を第1表(1)、(2)に示し、10
00℃における引張試験結果および1000℃における
103hr、104hrクリープ破断強度を第2表に示
した。
These component compositions are shown in Table 1 (1) and (2), and 10
Table 2 shows the tensile test results at 00°C and the 103hr and 104hr creep rupture strengths at 1000°C.

これらの試験結果より本発明合金は何れも従来合金およ
び比較合金(合金X、Y)よりクリープ破断強度がかな
り改善されていることが分る。
These test results show that the creep rupture strength of the alloys of the present invention is considerably improved over the conventional alloys and comparative alloys (alloys X and Y).

上記第2表の結果中、Mo、W添加鋼の結果を第1図に
、B、Zr添加鋼の結果を第2図に示した。
Among the results in Table 2 above, the results for Mo and W added steel are shown in FIG. 1, and the results for B and Zr added steel are shown in FIG.

Mへ Wの効果については第1図に示した103hr、
104hrクリープ破断強度とM。
To M Regarding the effect of W, 103hr shown in Figure 1,
104hr creep rupture strength and M.

+W量との関係図から明かである。This is clear from the relationship diagram with +W amount.

第1図における夫々の記号は下表の通りである。The respective symbols in FIG. 1 are as shown in the table below.

また第2図に示したように硼素(B)添加の影響につい
ては本発明合金A、F、W問および合金E。
Furthermore, as shown in FIG. 2, the effect of boron (B) addition was observed on alloys A, F, and W of the present invention and alloy E.

J、に、V間の比較により、そしてZr添加の影響につ
いては合金R,S、V間および合金H1■、M、RlT
、U間の比較により明かなように著しい強度改善効果が
あることがわかる。
Comparisons between alloys R, S, and V and alloys H1, M, and RlT indicate the effects of Zr addition.
, U clearly shows that there is a significant strength improvement effect.

第2図において、○、zr単独添加、・、B、Zr複合
添加(B≒0.004%)を示す。
In Fig. 2, ◯ indicates the addition of Zr alone, ., B indicates the combined addition of Zr (B≈0.004%).

このように本発明によって従来の合金よりも高温強度の
高い有望な耐熱合金を提供することが可能である。
As described above, the present invention makes it possible to provide a promising heat-resistant alloy that has higher high-temperature strength than conventional alloys.

【図面の簡単な説明】 第1図はMo、W添加鋼のクリープ破断強度を示す図、
第2図はB 、Zr添加鋼のクリープ破断強度を示す図
である。
[Brief explanation of the drawings] Figure 1 is a diagram showing the creep rupture strength of Mo and W added steel.
FIG. 2 is a diagram showing the creep rupture strength of B, Zr-added steel.

Claims (1)

【特許請求の範囲】 1C,0,01〜0.3%、Si、0.01〜1.0%
、4Mn、0.01〜2.0%、Cr、10〜30%、
Mg、0.003〜0.05%及びMo、3〜25%、
W、3〜25%の何れか一方又は両方(但しM。 及びWの両方を含む場合にはMoとWの合計で3〜25
チ)を含有し、残部はNi(但しNi、10、チ以下を
Feと置換できる。 )と不可避的不純物よりなり、Cが固溶したオーステナ
イト組織を有する耐熱合金。 2C,0,01〜0.3%、Si、0.01〜1.0%
、MnX0.01〜2.0%、Cr110〜30%、M
P、0.003〜0.05%及びMo13〜25%、W
、3〜2.5%の何れか一方又は両方(但し、MoとW
の両方を含む場合にはMoとWの合計で3〜25係。 )を含有し、更にB、0.001〜0.05%、Zr、
0.001〜1.0%の何れか一方又は両方を含有して
残部はNi(但しNi10%以下をFeと置換できる。 )と不可避的不純物とよりなり、Cが固溶したオーステ
ナイト組織を有する耐熱合金。
[Claims] 1C, 0.01-0.3%, Si, 0.01-1.0%
, 4Mn, 0.01-2.0%, Cr, 10-30%,
Mg, 0.003-0.05% and Mo, 3-25%,
W, either one or both of 3 to 25% (however, if both M and W are included, the total of Mo and W is 3 to 25%)
A heat-resistant alloy containing 1), the remainder being Ni (however, Ni (10% or less can be replaced with Fe)) and inevitable impurities, and having an austenitic structure in which C is dissolved as a solid solution. 2C, 0.01-0.3%, Si, 0.01-1.0%
, MnX0.01-2.0%, Cr110-30%, M
P, 0.003-0.05% and Mo13-25%, W
, 3 to 2.5% or both (however, Mo and W
If both are included, the total number of Mo and W is 3 to 25. ), and further contains B, 0.001 to 0.05%, Zr,
Contains either or both of 0.001 to 1.0%, with the remainder consisting of Ni (however, 10% or less of Ni can be replaced with Fe) and unavoidable impurities, and has an austenitic structure in which C is solidly dissolved. Heat resistant alloy.
JP1020375A 1975-01-23 1975-01-23 Tainetsugoukin Expired JPS58500B2 (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP1020375A JPS58500B2 (en) 1975-01-23 1975-01-23 Tainetsugoukin

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP1020375A JPS58500B2 (en) 1975-01-23 1975-01-23 Tainetsugoukin

Publications (2)

Publication Number Publication Date
JPS5184722A JPS5184722A (en) 1976-07-24
JPS58500B2 true JPS58500B2 (en) 1983-01-06

Family

ID=11743704

Family Applications (1)

Application Number Title Priority Date Filing Date
JP1020375A Expired JPS58500B2 (en) 1975-01-23 1975-01-23 Tainetsugoukin

Country Status (1)

Country Link
JP (1) JPS58500B2 (en)

Families Citing this family (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS5227014A (en) * 1975-08-27 1977-03-01 Japan Atom Energy Res Inst High temperature corrosion resisting ni-base alloy

Also Published As

Publication number Publication date
JPS5184722A (en) 1976-07-24

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