JPH07300653A - High strength steel bar excellent in delayed fracture resistance and its production - Google Patents

High strength steel bar excellent in delayed fracture resistance and its production

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Publication number
JPH07300653A
JPH07300653A JP11194394A JP11194394A JPH07300653A JP H07300653 A JPH07300653 A JP H07300653A JP 11194394 A JP11194394 A JP 11194394A JP 11194394 A JP11194394 A JP 11194394A JP H07300653 A JPH07300653 A JP H07300653A
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JP
Japan
Prior art keywords
delayed fracture
steel
fracture resistance
less
temperature
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
JP11194394A
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Japanese (ja)
Other versions
JP3153072B2 (en
Inventor
Shingo Yamazaki
真吾 山崎
Toshihiko Takahashi
稔彦 高橋
Toshizo Tarui
敏三 樽井
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
Nippon Steel Corp
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Filing date
Publication date
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Priority to JP11194394A priority Critical patent/JP3153072B2/en
Publication of JPH07300653A publication Critical patent/JPH07300653A/en
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Publication of JP3153072B2 publication Critical patent/JP3153072B2/en
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Expired - Lifetime legal-status Critical Current

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Abstract

PURPOSE:To increase the aspect ratio of old austenite grains, to refine the carbide grains precipitated in crystalline grain boundaries, and to provide superior delayed fracture resistance and high strength by subjecting a steel of specific composition to controlled rolling and then applying direct quenching and tempering treatment to the resulting rolled stock. CONSTITUTION:This steel has a composition consisting of, by weight ratio, 0.15-0.50% C, 0.1-2.0% Si, 0.05-2.0% Mn, <=0.015% P, <=0.02% S, 0.005-0.1% Al, and the balance Fe with inevitable impurities. Further, the steel has a structure consisting of tempered martensite and having >=2 length-to-width ratio, that is, aspect ratio of old austenite grains, <=0.2mum size of carbides in grain boundaries, and >=145kgf/mm<2> strength. Therefore, the steel is applied with a draft of 30% at 700-850 deg.C at the time of hot rolling to form a martensitic structure, then immediately subjected, to temp. rising at >=50 deg.C/sec heating rate, held at 350-500 deg.C for 10-50sec, and tempered.

Description

【発明の詳細な説明】Detailed Description of the Invention

【0001】[0001]

【産業上の利用分野】本発明は耐遅れ破壊特性に優れた
高張力鋼棒の製造に適用するものである。具体的にはJ
IS G 3109 D種 1号 SBPD 130/
145相当のPC鋼棒の耐遅れ破壊特性の改善に関す
る。
BACKGROUND OF THE INVENTION The present invention is applied to the production of high-strength steel rods having excellent delayed fracture resistance. Specifically, J
IS G 3109 Class D No. 1 SBPD 130 /
The present invention relates to improvement of delayed fracture resistance of a PC steel rod equivalent to 145.

【0002】[0002]

【従来の技術】PCパイルにはパイルのひび割れ防止、
曲げ強さ確保のため、PC鋼棒が補強材として用いられ
る。PCパイルの製造工程においてはまず、PC鋼棒に
よって鉄筋籠を形成し、このPC鋼棒に引張強さの70
%の引張応力を負荷し、この籠を型枠内に配置し、コン
クリート原料を型枠内に投入し、遠心成形することによ
って製造される。ここにおいて、引張応力を負荷された
PC鋼棒はコンクリートに圧縮応力を与えることによっ
て、コンクリートのひび割れを防ぐ作用を持つ。PC鋼
棒は強度が145kgf/mm2 以上と高いうえに、コ
ンクリート中で強度の70%の張力を負荷された状態で
使用されるため、遅れ破壊が発生する可能性が高い。こ
のため、耐遅れ破壊特性の優れた鋼棒が必要となる。
2. Description of the Related Art PC piles are used to prevent cracks in the piles.
PC steel rod is used as a reinforcing material to secure bending strength. In the process of manufacturing a PC pile, first, a rebar cage is formed from a PC steel rod, and a tensile strength of 70 is applied to the PC steel rod.
% Tensile stress, the cage is placed in a mold, concrete raw material is put into the mold, and centrifugal molding is performed. Here, the PC steel rod loaded with tensile stress has an action of preventing cracking of concrete by giving compressive stress to concrete. Since the PC steel rod has a high strength of 145 kgf / mm 2 or more and is used in a state of being loaded with a tension of 70% of the strength in concrete, delayed fracture is likely to occur. Therefore, a steel rod having excellent delayed fracture resistance is required.

【0003】遅れ破壊は粒界破壊が支配的であるため、
旧オーステナイト粒を微細化する対策(特開平5−17
1356号公報)や、焼戻し温度を高くする対策(特開
平5−117811号公報)等が取られている。また、
遅れ破壊の原因となる水素の侵入を抑制するため、合金
元素の添加により耐腐食特性を向上させることも試みら
れている(特開平2−240236号公報、特開平2−
240237号公報、特開平2−240244号公
報)。更に合金元素の添加による高温焼戻しが耐遅れ破
壊特性を向上させるという提案もある。
Delayed fracture is dominated by grain boundary fracture, so
Measures for refining old austenite grains (Japanese Patent Application Laid-Open No. 5-17
1356), and measures for increasing the tempering temperature (JP-A-5-117811). Also,
In order to suppress the penetration of hydrogen, which causes delayed fracture, it has also been attempted to improve the corrosion resistance by adding an alloying element (JP-A-2-240236 and JP-A-2-24036).
No. 240237 and Japanese Patent Laid-Open No. 2-240244). There is also a proposal that high-temperature tempering by adding alloy elements improves delayed fracture resistance.

【0004】[0004]

【発明が解決しようとする課題】しかしながら、上記の
いずれの方法も遅れ破壊の特徴である粒界破壊の抑制は
不十分で、耐遅れ破壊特性向上には完全とは言えない。
そこで本発明は上記のような事情に着目してなされたも
のであって、その目的は旧オーステナイト粒のアスペク
ト比、及び粒界炭化物のサイズを制御することによって
遅れ破壊感受性が低い高強度棒鋼を提供しようとするも
のである。
However, none of the above-mentioned methods is sufficient for suppressing the intergranular fracture, which is a characteristic of delayed fracture, and is not perfect for improving delayed fracture resistance.
Therefore, the present invention has been made in view of the above circumstances, and its purpose is to provide a high strength steel bar with low delayed fracture susceptibility by controlling the aspect ratio of old austenite grains and the size of grain boundary carbides. It is the one to be provided.

【0005】[0005]

【課題を解決するための手段】本発明者らは、高強度鋼
材の遅れ破壊現象をシミュレーションでき、しかも遅れ
破壊特性を破壊に要する水素量で評価できる遅れ破壊試
験法を開発した。この方法を用いた試験結果から、棒鋼
の熱処理における焼戻しの際の加熱速度と保持温度、保
持時間の制御により遅れ破壊に要する水素量を増加でき
る、つまり耐遅れ破壊特性を改善できるとの知見を得
て、本発明を完成するに至ったものである。
The present inventors have developed a delayed fracture test method capable of simulating the delayed fracture phenomenon of a high strength steel and evaluating the delayed fracture characteristics by the amount of hydrogen required for fracture. From the test results using this method, it was found that the hydrogen rate required for delayed fracture can be increased by controlling the heating rate, holding temperature, and holding time during tempering in the heat treatment of steel bars, that is, the delayed fracture resistance can be improved. Thus, the present invention has been completed.

【0006】その要旨とするところは、C:0.15〜
0.50%、Si:0.1〜2.0%、Mn:0.05
〜2.0%、P:0.015%以下、S:0.02%以
下、Al:0.005〜0.1%を含有し、さらに必要
に応じCr:0.1〜3.0%、Mo:0.05〜1.
2%、Ni:0.05〜2.0%、V:0.10〜0.
50%、Ti:0.005〜0.10%、Nb:0.0
05〜0.10%のうち1種または2種以上を含有し、
残部がFeおよび不可避的不純物よりなる鋼で、焼戻し
マルテンサイト組織からなり、旧オーステナイト粒のア
スペクト比が2以上であるとともに旧オーステナイト粒
界の炭化物のサイズが0.05〜0.2μmであり、且
つ強度が145kgf/mm2 以上であることを特徴と
する耐遅れ破壊特性に優れた高強度鋼棒であり、さらに
上記成分の鋼を熱間圧延する際に温度700℃以上85
0℃以下の温度域で30%以上の圧下率を与える工程を
経た後、直ちに水冷してマルテンサイト組織にした後、
50℃/sec以上の加熱速度で昇温し、350℃〜5
00℃の温度範囲に10〜50秒保持して焼戻すことを
特徴とする耐遅れ破壊特性に優れた高強度鋼棒の製造方
法である。
The gist of the matter is that C: 0.15 to 0.15.
0.50%, Si: 0.1-2.0%, Mn: 0.05
.About.2.0%, P: 0.015% or less, S: 0.02% or less, Al: 0.005 to 0.1%, and if necessary, Cr: 0.1 to 3.0%. , Mo: 0.05-1.
2%, Ni: 0.05 to 2.0%, V: 0.10 to 0.
50%, Ti: 0.005 to 0.10%, Nb: 0.0
It contains one or more of 05 to 0.10%,
The balance is steel consisting of Fe and unavoidable impurities, consisting of a tempered martensite structure, the aspect ratio of the former austenite grains is 2 or more, and the size of the carbide of the former austenite grain boundaries is 0.05 to 0.2 μm, And a strength of 145 kgf / mm 2 or more, which is a high-strength steel rod excellent in delayed fracture resistance, and a temperature of 700 ° C. or more 85
After a step of giving a rolling reduction of 30% or more in a temperature range of 0 ° C. or less, immediately after water cooling to form a martensite structure,
The temperature is raised at a heating rate of 50 ° C./sec or more to 350 ° C. to 5
A method for producing a high-strength steel rod excellent in delayed fracture resistance, characterized by holding in a temperature range of 00 ° C for 10 to 50 seconds and tempering.

【0007】[0007]

【作用】この遅れ破壊試験方法は図1の形状の環状ノッ
チをもつPC鋼棒からなる供試材に定電流陰極チャージ
によって水素をチャージした後、大気中で図2で示され
るカンチレバー式の試験機によって引張強度の70%の
定荷重引張応力を負荷し、破断に要する時間を測定する
ものである。他方、これと同一形状の供試材に同一条件
で陰極チャージを行い、この供試材にチャージされた水
素量をガスクロマトグラフ法により測定する。このと
き、100℃/hourの昇温速度で加熱し測定を行う
が、水素の放出プロファイルには図3のように2つのピ
ークが現れる。このうちの低温側のピークは室温で拡散
し得る水素量を示すため、これを拡散性水素量と定義す
る。
The delayed fracture test method is the cantilever type test shown in FIG. 2 in the atmosphere after hydrogen is charged by the constant current cathodic charge to the specimen made of PC steel rod having the annular notch of the shape shown in FIG. With a machine, a constant load tensile stress of 70% of the tensile strength is applied, and the time required for breaking is measured. On the other hand, a sample material having the same shape as this is subjected to cathode charging under the same conditions, and the amount of hydrogen charged in the sample material is measured by a gas chromatograph method. At this time, measurement is performed by heating at a temperature rising rate of 100 ° C./hour, but two peaks appear in the hydrogen release profile as shown in FIG. Since the peak on the low temperature side shows the amount of hydrogen that can diffuse at room temperature, this is defined as the amount of diffusible hydrogen.

【0008】こうして求めた破断時間とそのときの拡散
性水素量をグラフ化すると図4の様になる。この図から
負荷後100時間たっても破断しない水素量Hcを求
め、これを限界拡散性水素量と定義し、この大小で鋼材
の耐遅れ破壊特性を判断する。この遅れ破壊試験方法に
よってPC鋼棒での遅れ破壊クラックの発生と伝播現象
を調査した結果、次のことが判明した。すなわち、圧延
仕上げ温度を未再結晶温度域である700℃以上850
℃以下としこの温度域での圧下率を30%以上、好まし
くは50%以上とし、且つ冷却温度を150℃/sec
以上の範囲にして冷却することによって表層から少なく
とも0.5mm以上の深さまでの旧オーステナイト結晶
粒が伸長化され、アスペクト比が2以上、前記の好まし
い条件下で4以上であるマルテンサイト組織を得る。こ
れを50℃/sec以上、好ましくは100℃/sec
以上の加熱速度で昇温し、350℃〜500℃の温度範
囲に10秒〜50秒、好ましくは10〜20秒の時間保
持して焼戻すことにより、旧オーステナイト粒界上に析
出する炭化物が成長するに十分な時間がないため、普通
の焼戻しで粒界炭化物サイズは0.4μm程度であるの
に対して、0.2μm以下、前記の好ましい条件下では
0.1μm以下という微少な粒界炭化物をもつ焼戻しマ
ルテンサイト組織を得る。このような微細な粒界炭化物
を特徴とする組織を持つ鋼では、亀裂が旧オーステナイ
ト粒界に沿って伝播することが困難であり、したがって
粒界破壊するに際し多量の拡散性水素を必要とする、す
なわち、耐遅れ破壊特性が大幅に改善できることを見出
したのである。
The breaking time thus obtained and the amount of diffusible hydrogen at that time are plotted in a graph as shown in FIG. From this figure, the hydrogen amount Hc that does not fracture even after 100 hours from loading is determined, and this is defined as the limit diffusible hydrogen amount, and the delayed fracture resistance property of the steel material is judged by this amount. As a result of investigating the occurrence and propagation phenomenon of the delayed fracture crack in the PC steel rod by this delayed fracture test method, the following was found. That is, the rolling finishing temperature is 700 ° C. or higher and 850 ° C. which is a non-recrystallization temperature range.
C. or less, the rolling reduction in this temperature range is 30% or more, preferably 50% or more, and the cooling temperature is 150 ° C./sec.
By cooling in the above range, the prior austenite crystal grains from the surface layer to a depth of at least 0.5 mm are elongated, and a martensite structure having an aspect ratio of 2 or more and 4 or more under the above preferable conditions is obtained. . 50 ° C / sec or more, preferably 100 ° C / sec
By heating at the above heating rate and holding in a temperature range of 350 ° C. to 500 ° C. for 10 seconds to 50 seconds, preferably 10 to 20 seconds and tempering, carbides precipitated on the former austenite grain boundaries are Since there is not enough time to grow, the grain boundary carbide size is about 0.4 μm in ordinary tempering, while the grain boundary carbide size is 0.2 μm or less, and a minute grain boundary of 0.1 μm or less under the above preferable conditions. A tempered martensitic structure with carbides is obtained. In a steel having a structure characterized by such fine grain boundary carbides, it is difficult for cracks to propagate along the former austenite grain boundary, and therefore a large amount of diffusible hydrogen is required for grain boundary fracture. That is, they have found that the delayed fracture resistance can be greatly improved.

【0009】これらの実験及び検討の結果本発明を完成
したものであって、本発明に従う高強度鋼棒の合金成分
の範囲は次の理由で決定される。Cは、焼入れ、焼戻し
により高強度を得るためには0.15%以上必要である
が、0.5%を超えると靱性を劣化させるとともに耐遅
れ破壊特性も劣化させる元素であるために0.15%以
上0.50%以下とした。Siは鋼の脱酸および強度を
高めるのに必要な元素であり、0.1%以上添加する。
2.0%を超えると脆化の原因となるので、0.1%以
上2.0%以下とした。Mnは鋼の脱酸および焼入れ性
の確保のため0.05%以上必要であり、2.0%を超
えるとオーステナイト域加熱時に粒界に偏析し粒界を脆
化させるとともに耐遅れ破壊特性を劣化させる元素であ
るために0.05%以上2.0%以下とした。
As a result of these experiments and examinations, the present invention has been completed, and the range of alloy components of the high strength steel rod according to the present invention is determined for the following reason. C is required to be 0.15% or more in order to obtain high strength by quenching and tempering, but if it exceeds 0.5%, it is an element that deteriorates toughness and delayed fracture resistance, and therefore, is 0.1. It was set to 15% or more and 0.50% or less. Si is an element necessary for increasing the deoxidation and strength of steel, and is added in an amount of 0.1% or more.
If it exceeds 2.0%, it causes embrittlement, so the content was made 0.1% to 2.0%. Mn is required to be 0.05% or more in order to secure the deoxidation and hardenability of steel, and if it exceeds 2.0%, it segregates to the grain boundaries during heating in the austenite region and embrittles the grain boundaries, and also provides delayed fracture resistance. Since it is an element that deteriorates, it is set to 0.05% to 2.0%.

【0010】Pは焼入れ性元素としては有効であるが、
凝固時にミクロ偏析し、さらにオーステナイト域加熱時
に粒界に偏析し粒界を脆化させるとともに耐遅れ破壊特
性を劣化させる元素であるために0.015%以下とし
た。Sは不可避的不純物であるが、オーステナイト域加
熱時に粒界に偏析し粒界を脆化させるとともに耐遅れ破
壊特性を劣化させる元素であるために0.02%以下と
した。Alは鋼の脱酸に有効な元素であるために0.0
05%以上必要であるが、0.1%を超えると靱性の劣
化を招くために0.005%以上0.1%以下とした。
Although P is effective as a hardenable element,
Since it is an element that causes micro-segregation during solidification and further segregates at grain boundaries during heating in the austenite region to embrittle the grain boundaries and deteriorate delayed fracture resistance, the content was made 0.015% or less. Although S is an unavoidable impurity, it is an element that segregates at the grain boundaries during heating in the austenite region, embrittles the grain boundaries, and deteriorates the delayed fracture resistance. Since Al is an element effective for deoxidizing steel, 0.0
It is necessary to be 05% or more, but if it exceeds 0.1%, the toughness is deteriorated, so the content was made 0.005% or more and 0.1% or less.

【0011】また、耐遅れ破壊特性に及ぼす合金元素、
焼戻し温度の影響を調べたところ、従来の高強度棒鋼に
比べて、Cr、Mo、Ni、V、Ti、Nbの添加が有
効であることを見出した。従って、必要に応じこれらの
元素の内、1種または2種以上を含有させる。
Further, alloying elements which affect delayed fracture resistance,
When the influence of the tempering temperature was investigated, it was found that the addition of Cr, Mo, Ni, V, Ti and Nb was more effective than the conventional high strength steel bar. Therefore, if necessary, one kind or two or more kinds of these elements are contained.

【0012】Crは鋼の焼入れ性を得るためには0.1
%以上必要であるが、多すぎると靱性の劣化、冷間加工
性の劣化を招く元素であるために3.0%以下とした。
Moは鋼の焼入れ性を得るために、また焼戻し軟化抵抗
を有し400℃以上の焼戻し温度で安定して145kg
f/mm2 以上の引張荷重を得るのに0.05%以上必
要な元素であり、1.2%を超えるとその効果は飽和し
コストの上昇を招くために0.05%以上1.2%以下
とした。Niは靱性を向上させるとともに耐遅れ破壊特
性を向上させるために0.05%以上必要であるが、
2.0%を超えるとその効果は飽和しむしろコスト上昇
を招くために0.05%以上2.0%以下とした。
Cr is 0.1 in order to obtain hardenability of steel.
% Or more, but if it is too much, it is an element that causes deterioration of toughness and cold workability, so the content was made 3.0% or less.
Mo has a tempering softening resistance in order to obtain the hardenability of steel, and is stable at a tempering temperature of 400 ° C. or higher and is stable at 145 kg.
It is an element that is required to be 0.05% or more to obtain a tensile load of f / mm 2 or more, and when it exceeds 1.2%, its effect is saturated and the cost increases, so 0.05% or more 1.2 % Or less. Ni is required to be 0.05% or more in order to improve toughness and delayed fracture resistance,
If it exceeds 2.0%, the effect is saturated and rather the cost is increased, so the content is made 0.05% or more and 2.0% or less.

【0013】V、Ti、Nbは、結晶粒の微細化に寄与
し、かつ水素との親和性に富み鋼中での水素の拡散・集
積を抑制することにより耐遅れ破壊特性向上に有効な元
素であるため、それぞれV:0.10%以上、Ti:
0.005%以上、Nb:0.005%以上必要であ
る。ただし多すぎるとその効果は飽和しむしろ靱性を劣
化させる元素であるためにそれぞれV:0.50%以
下、Ti:0.10%以下、Nb:0.10%以下とし
た。
V, Ti, and Nb are elements effective for improving the delayed fracture resistance by contributing to the refinement of crystal grains and having a high affinity with hydrogen, and suppressing the diffusion and accumulation of hydrogen in steel. Therefore, V: 0.10% or more and Ti:
0.005% or more and Nb: 0.005% or more are required. However, if it is too large, the effect is saturated and rather it is an element that deteriorates toughness, so V: 0.50% or less, Ti: 0.10% or less, and Nb: 0.10% or less, respectively.

【0014】次に本発明で目的とする高強度のPC鋼棒
遅れ破壊特性の向上に対して最も重要な点である旧オー
ステナイト粒のアスペクト比と、粒界炭化物サイズの限
定理由について述べる。図5に焼戻しマルテンサイト組
織からなるPC鋼棒の限界拡散水素量に及ぼす旧オース
テナイト粒のアスペクト比の影響について解析した一例
を示す。アスペクト比が2未満では限界拡散性水素量の
向上効果が少ない、即ち遅れ破壊特性向上効果が少ない
ため、アスペクト比を2以上に限定した。
Next, the aspect ratio of the former austenite grains and the reasons for limiting the grain boundary carbide size, which are the most important points for improving the delayed fracture properties of high strength PC steel rods aimed at by the present invention, will be described. FIG. 5 shows an example of analysis of the effect of the aspect ratio of the prior austenite grains on the critical diffusion hydrogen amount of the PC steel rod having the tempered martensite structure. When the aspect ratio is less than 2, the effect of improving the limit diffusible hydrogen amount is small, that is, the effect of improving the delayed fracture property is small. Therefore, the aspect ratio is limited to 2 or more.

【0015】また、図6に焼戻しマルテンサイト組織か
らなるPC鋼棒の限界拡散性水素量に及ぼす粒界炭化物
サイズの影響について解析した一例を示す。粒界炭化物
サイズが0.2μm超では限界拡散性水素量の向上効果
が少ない。即ち遅れ破壊特性向上効果が少ないため、粒
界炭化物サイズを0.2μm以下に限定した。この2つ
のパラメータが限界拡散水素量に及ぼす影響を解析した
一例を図7に示す。アスペクト比を2以上にし、かつ粒
界炭化物サイズを0.2μm以下にすることによって限
界拡散性水素量を増加させることができる。したがって
アスペクト比2以上で且つ粒界炭化物サイズを0.2μ
m以下に限定した。
FIG. 6 shows an example of the analysis of the effect of grain boundary carbide size on the critical diffusible hydrogen content of a PC steel rod having a tempered martensite structure. If the grain boundary carbide size exceeds 0.2 μm, the effect of improving the critical diffusible hydrogen amount is small. That is, since the effect of improving delayed fracture characteristics is small, the grain boundary carbide size is limited to 0.2 μm or less. An example of analyzing the effect of these two parameters on the limit diffusion hydrogen amount is shown in FIG. The critical diffusible hydrogen content can be increased by setting the aspect ratio to 2 or more and the grain boundary carbide size to 0.2 μm or less. Therefore, the aspect ratio is 2 or more and the grain boundary carbide size is 0.2μ.
It was limited to m or less.

【0016】本発明の高強度PC鋼棒の製造方法では、
所定の条件で熱間圧延を行った後、直ちに焼入れてマル
テンサイト組織にした後、所定の加熱速度、温度、保持
時間で焼戻しを行うものであるが、次にこの製造条件の
限定理由について述べる。 加熱速度;加熱速度が50℃/sec未満では、昇温の
過程で粒界炭化物が析出、粗大化するため安定して微細
な粒界炭化物を得ることが困難であるため加熱速度の下
限を50℃/secとした。 圧延温度;圧延温度が850℃を超えると圧延時の再結
晶が顕著になり、アスペクト比が2以上のマルテンサイ
ト組織を得ることが困難である。一方、圧延温度が70
0℃未満では所定のアスペクト比の組織を得るに十分な
圧下率を確保できない。従って圧延温度を700℃以上
850℃に限定した。 圧下率;アスペクト比が2以上のマルテンサイト組織を
得るには30%以上の圧下率が必要であるため圧下率を
30%以上に限定した。 加熱温度;350℃未満の温度では粒界脆化が顕著にな
り、遅れ破壊特性が悪化する。500℃を超える温度で
は強度が低下し、また安定して微細な粒界炭化物を得る
ことが困難なため、加熱温度域を350℃以上500℃
以下とした。 保持時間;50秒を超える時間保持すると、炭化物が粗
大化する。一方、10秒未満の短時間では均一な焼戻し
マルテンサイト組織を得ることが困難である。従って1
0秒以上50秒以下に限定した。
In the method for producing a high strength PC steel rod of the present invention,
After hot rolling under predetermined conditions, immediately after quenching to a martensite structure, tempering is performed at a predetermined heating rate, temperature, and holding time.Next, the reasons for limiting the manufacturing conditions will be described. . Heating rate; If the heating rate is less than 50 ° C./sec, grain boundary carbides precipitate and coarsen during the temperature rising process, and it is difficult to stably obtain fine grain boundary carbides. Therefore, the lower limit of the heating rate is 50. C / sec. Rolling temperature: When the rolling temperature exceeds 850 ° C., recrystallization during rolling becomes remarkable, and it is difficult to obtain a martensite structure having an aspect ratio of 2 or more. On the other hand, the rolling temperature is 70
If it is less than 0 ° C., it is impossible to secure a sufficient reduction rate to obtain a structure having a predetermined aspect ratio. Therefore, the rolling temperature is limited to 700 ° C or higher and 850 ° C. Reduction ratio: Since a reduction ratio of 30% or more is required to obtain a martensite structure having an aspect ratio of 2 or more, the reduction ratio is limited to 30% or more. Heating temperature: If the temperature is lower than 350 ° C, embrittlement of grain boundaries becomes significant, and delayed fracture characteristics deteriorate. At temperatures above 500 ° C, the strength decreases and it is difficult to stably obtain fine grain boundary carbides.
Below. Retention time; When retained for more than 50 seconds, carbides coarsen. On the other hand, in a short time of less than 10 seconds, it is difficult to obtain a uniform tempered martensite structure. Therefore 1
It was limited to 0 seconds to 50 seconds.

【0017】[0017]

【実施例】供試鋼の化学成分を表1に、熱処理条件、降
伏点、引張強度、伸び、並びに上記の遅れ破壊試験によ
り求めた限界拡散性水素量を表2に示す。(1)〜(2
0)は本発明の高張力鋼棒用鋼の成分、熱処理条件に従
ったものであり、(21)〜(43)は比較鋼である。
直径7.4mmに所定の条件で圧延後直ちに水冷し、そ
の後高周波加熱炉によって焼戻しを行った。熱処理条件
は、JIS D種1号 SBPD 130/145相当
の引張強度となるように行った。
[Examples] Table 1 shows the chemical composition of the sample steel, and Table 2 shows the heat treatment conditions, the yield point, the tensile strength, the elongation, and the critical diffusible hydrogen content obtained by the delayed fracture test. (1) ~ (2
0) is in accordance with the components and heat treatment conditions of the steel for high-strength steel rod of the present invention, and (21) to (43) are comparative steels.
Immediately after rolling to a diameter of 7.4 mm under a predetermined condition, it was water-cooled and then tempered in a high-frequency heating furnace. The heat treatment conditions were such that the tensile strength was equivalent to JIS D type 1 SBPD 130/145.

【0018】[0018]

【表1】 [Table 1]

【0019】[0019]

【表2】 [Table 2]

【0020】この表より、本発明の組成および焼戻し温
度、焼戻し速度の範囲にある(1)〜(20)は、比較
材である(21)〜(43)に比べて限界水素量が高
く、遅れ破壊しにくいこと、あるいは比較材は添加元素
が少なくその効果が見られないことが明らかである。
From this table, (1) to (20) in the composition, tempering temperature, and tempering speed range of the present invention have a higher limit hydrogen content than the comparative materials (21) to (43). It is clear that delayed fracture is unlikely to occur, or that the comparative material has few added elements and its effect cannot be seen.

【0021】[0021]

【発明の効果】本発明によりアスペクト比、粒界炭化物
のサイズを制御することによって、JIS G 310
9 D種 1号 SBPD 130/145相当の引張
強度を有し、耐遅れ破壊特性の優れたPC鋼棒を製造す
る。
According to the present invention, by controlling the aspect ratio and the size of grain boundary carbides, JIS G 310
9 Type D No. 1 SBPD 130/145 equivalent tensile strength and PC steel bar excellent in delayed fracture resistance are manufactured.

【図面の簡単な説明】[Brief description of drawings]

【図1】鋼材の遅れ破壊試験に用いた試験片の平面図FIG. 1 is a plan view of a test piece used for a delayed fracture test of steel materials.

【図2】遅れ破壊試験装置の説明図FIG. 2 is an explanatory diagram of a delayed fracture test device.

【図3】水素量分析の水素放出プロファイルFIG. 3 Hydrogen release profile of hydrogen content analysis

【図4】限界拡散性水素量の説明図FIG. 4 is an explanatory diagram of the limit diffusible hydrogen amount.

【図5】旧オーステナイト粒のアスペクト比が限界拡散
性水素量に及ぼす効果を示すグラフ
FIG. 5 is a graph showing the effect of the aspect ratio of old austenite grains on the critical diffusible hydrogen content.

【図6】粒界炭化物サイズが限界拡散性水素量に及ぼす
効果を示すグラフ
FIG. 6 is a graph showing the effect of grain boundary carbide size on the critical diffusible hydrogen content.

【図7】旧オーステナイト粒のアスペクト比と粒界炭化
物サイズが限界拡散性水素量に及ぼす効果を示すグラフ
FIG. 7 is a graph showing the effect of the aspect ratio of old austenite grains and the grain boundary carbide size on the critical diffusible hydrogen content.

【符号の説明】[Explanation of symbols]

1 試験片 2 バランスウェイト 3 支点 1 test piece 2 balance weight 3 fulcrum

Claims (4)

【特許請求の範囲】[Claims] 【請求項1】 重量%で C :0.15〜0.50% Si:0.1〜2.0% Mn:0.05〜2.0% P :0.015%以下 S :0.02%以下 Al:0.005〜0.1% を含有し、残部がFeおよび不可避的不純物よりなる鋼
で、焼戻しマルテンサイト組織からなり、旧オーステナ
イト粒の長さと幅の比(以降アスペクト比とする)が2
以上であるとともに粒界の炭化物のサイズが0.2μm
以下であり、且つ強度が145kgf/mm2 以上であ
ることを特徴とする耐遅れ破壊特性に優れた高強度鋼
棒。
1. C: 0.15 to 0.50% Si: 0.1 to 2.0% Mn: 0.05 to 2.0% P: 0.015% or less S: 0.02 % Or less Al: A steel containing 0.005 to 0.1% and the balance of Fe and unavoidable impurities. The steel has a tempered martensite structure and the ratio of the length to the width of the former austenite grains (hereinafter referred to as the aspect ratio). ) Is 2
And the size of carbides at grain boundaries is 0.2 μm
A high-strength steel rod excellent in delayed fracture resistance, characterized in that the strength is 145 kgf / mm 2 or more.
【請求項2】 請求項1の鋼成分に加え、さらに重量%
で Cr:0.1〜3.0% Mo:0.05〜1.2% Ni:0.05〜2.0% V :0.10〜0.50% Ti:0.005〜0.10% Nb:0.005〜0.10% のうち1種または2種以上を含有することを特徴とする
請求項1記載の耐遅れ破壊特性に優れた高強度鋼棒。
2. In addition to the steel composition according to claim 1, further% by weight
Cr: 0.1 to 3.0% Mo: 0.05 to 1.2% Ni: 0.05 to 2.0% V: 0.10 to 0.50% Ti: 0.005 to 0.10. % Nb: 0.005 to 0.10%, and one or more kinds are contained, The high strength steel rod excellent in delayed fracture resistance according to claim 1.
【請求項3】 重量%で C :0.15〜0.50% Si:0.1〜2.0% Mn:0.05〜2.0% P :0.015%以下 S :0.02%以下 Al:0.005〜0.1% を含有し、残部がFeおよび不可避的不純物よりなる鋼
を熱間圧延するに際して温度700℃以上850℃以下
の温度域で30%以上の圧下率を与える工程を経た後、
マルテンサイト組織にした後、50℃/sec以上の加
熱速度で昇温し、350℃〜500℃の温度範囲に10
〜50秒保持して焼戻すことを特徴とする耐遅れ破壊特
性に優れた高強度鋼棒の製造方法。
3. By weight%, C: 0.15 to 0.50% Si: 0.1 to 2.0% Mn: 0.05 to 2.0% P: 0.015% or less S: 0.02 % Or less Al: 0.005 to 0.1% is contained, and the balance of Fe and inevitable impurities is hot-rolled. When hot rolling, a reduction ratio of 30% or more in a temperature range of 700 ° C to 850 ° C is applied. After the giving process,
After forming the martensite structure, the temperature is raised at a heating rate of 50 ° C./sec or more, and the temperature is increased to 10 ° C. in the temperature range of 350 ° C. to 500 ° C.
A method for producing a high-strength steel rod excellent in delayed fracture resistance, characterized by holding for 50 seconds and tempering.
【請求項4】 請求項3の鋼成分に加え、さらに重量%
で Cr:0.1〜3.0% Mo:0.05〜1.2% Ni:0.05〜2.0% V :0.10〜0.50% Ti:0.005〜0.10% Nb:0.005〜0.10% のうち1種または2種以上を含有することを特徴とする
請求項3記載の耐遅れ破壊特性に優れた高強度鋼棒の製
造方法。
4. In addition to the steel composition according to claim 3, further% by weight
Cr: 0.1 to 3.0% Mo: 0.05 to 1.2% Ni: 0.05 to 2.0% V: 0.10 to 0.50% Ti: 0.005 to 0.10. % Nb: 0.005 to 0.10%, and one or more kinds are contained, The method for producing a high strength steel rod excellent in delayed fracture resistance according to claim 3.
JP11194394A 1994-04-28 1994-04-28 High-strength steel rod excellent in delayed fracture resistance and method of manufacturing the same Expired - Lifetime JP3153072B2 (en)

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JP11194394A JP3153072B2 (en) 1994-04-28 1994-04-28 High-strength steel rod excellent in delayed fracture resistance and method of manufacturing the same

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JPH07300653A true JPH07300653A (en) 1995-11-14
JP3153072B2 JP3153072B2 (en) 2001-04-03

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Cited By (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US6348108B1 (en) * 1998-03-04 2002-02-19 National Research Institute For Metals High toughness steel and a method for manufacturing the same
US7093526B2 (en) 1999-05-20 2006-08-22 Honda Giken Kogyo Kabushiki Kaisha Forming die apparatus
JP2008025010A (en) * 2006-07-25 2008-02-07 Ntn Corp Rolling parts and rolling bearing
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