JPWO2001066814A1 - Steel with excellent forgeability and machinability - Google Patents
Steel with excellent forgeability and machinabilityInfo
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- JPWO2001066814A1 JPWO2001066814A1 JP2001-565415A JP2001565415A JPWO2001066814A1 JP WO2001066814 A1 JPWO2001066814 A1 JP WO2001066814A1 JP 2001565415 A JP2001565415 A JP 2001565415A JP WO2001066814 A1 JPWO2001066814 A1 JP WO2001066814A1
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Abstract
(57)【要約】 最弱方向の機械的性質の低下を抑制して鍛造加工性を向上させつつ、被削性の良好な鋼で、重量%で、C:0.1〜0.85%、Si:0.01〜1.5%、Mn:0.05〜2.0%、P:0.003〜0.2%、S:0.003〜0.5%、Zr:0.0003〜0.01%を含有するとともにAl:0.01%以下、total−0:0.02%以下、total−N:0.02%以下を制限し、かつ、MnSの平均アスペクト比10以下、最大アスペクト比30以下を有し、残部がFeおよび不可避的不純物よりなることを特徴とする鍛造性と被削性に優れる鋼。 (57) [Abstract] A steel with excellent forgeability and machinability, which suppresses the deterioration of mechanical properties in the weakest direction and improves forgeability, and which contains, by weight, C: 0.1 to 0.85%, Si: 0.01 to 1.5%, Mn: 0.05 to 2.0%, P: 0.003 to 0.2%, S: 0.003 to 0.5%, Zr: 0.0003 to 0.01%, with Al: 0.01% or less, total-0: 0.02% or less, and total-N: 0.02% or less, and has an average aspect ratio of MnS of 10 or less, a maximum aspect ratio of 30 or less, and the balance being Fe and unavoidable impurities.
Description
技術分野
本発明は自動車や一般機械などに用いられる鋼に関するものであり、特に熱間
鍛造と被削性に優れた鋼に関するものである。
背景技術
近年鋼の高強度化が進む反面、加工性が低下するため、鍛造や切削能率の低下
させない鋼に対するニーズが高まっている。これまで熱間鍛造に対しては介在物
の低減、高温延性を増す元素の添加、高温延性阻害元素の低減などが一般的な対
策であった。一方、被削性を向上させるためにS,Pbなどの被削性向上元素を
添加するのが有効であることが知られているが、それら被削性向上に有効な元素
は高温延性を低下させるので、熱間鍛造と被削性の両立は困難である。Pb,B
iは被削性を向上し、鍛造への影響も比較的少ないとされているが、高温延性を
低減することが知られている。SはMnSのような切削環境下で軟質となる介在
物を形成して被削性を向上させるが、MnS寸法はPb等の粒子に比べて大きく
、応力集中元となり易い。特に鍛造や圧延によりMnSは伸延すると異方性を生
じ、特定の方向に極端に弱くなる。また設計上もその様な異方性を考慮する必要
が生じる。したがってこのような快削元素の異方性を最低限にする技術が必要に
なる。またPに関しても被削性を向上させることが知られているが、熱間鋳造時
に割れを生じ易いために多く添加することが出来ず、被削性向上効果にも限界が
ある。Teを添加すれば異方性が解消されることが主張されているが(特開昭5
5−41943)、Teは鋳造時および圧延、鍛造時に割れを生じ易い。
また、鋼中にZr,Caを含む脱酸剤を添加して、鋼の被削性を低速から高速
切削の広い範囲にわたって改善を図った特開昭49−66522号公報に開示さ
れた技術がある。しかしながら、この技術においても圧延または鍛造により延伸
されたMnSによる破壊の問題は依然として解決されていない。
そこでこのような熱間延性と被削性を両立するにはさらなる技術革新が必要で
ある。
発明の開示
本発明は上記実状に対応するため、熱間延性と被削性の良好な鋼を提供するこ
とを目的とするものである。
一般に鋼は圧延や鍛造により加工が加わるが、その際の塑性流動により、機械
的性質に異方性を生じる。鍛造時にはその異方性に起因する割れが実質の鍛造限
界を示す。したがって鍛造性を向上させるにはMnSのような介在物の形状を極
力球形に近くし、異方性を最低限に抑制することが有効である。またたとえ異方
性を生じても介在物の寸法が小さければ、異方性の影響は小さく出来る。そのた
め、被削性を向上させるMnSを微細に分散し、かつその形状を球状に維持する
ための鋼材成分とすることが望ましい。
本発明は以上の知見に基づいてなされた鍛造性と被削性に優れた鋼であって、
その要旨は以下に示すとおりである。
(1)質量%で、
C :0.1〜0.85%、
Si:0.01〜1.5%、
Mn:0.05〜2.0%、
P :0.003〜0.2%、
S :0.003〜0.5%、
Zr:0.0003〜0.01%
を含有するとともに
Al:0.01%以下、
total−O:0.02%以下、
total−N:0.02%以下
に制限し、かつ、MnSの平均アスペクト比10以下で、最大アスペクト比30
以下を有し、残部がFeおよび不可避的不純物よりなることを特徴とする鍛造性
と被削性に優れた鋼。
(2)質量%で、
C :0.1〜0.85%、
Si:0.01〜1.5%、
Mn:0.05〜2.0%、
P :0.003〜0.2%、
S :0.003〜0.5%、
Zr:0.0003〜0.01%
を含有するとともに
Al:0.01%以下、
total−O:0.02%以下、
total−N:0.02%以下
に制限し、かつ、MnSの平均アスペクト比10以下で、最大アスペクト比30
以下を有し、更に最大MnS粒径(μm)が110×〔S%〕−15以下、1m
m2あたりのMnS数が3800×〔S%〕−150以下を有し、残部がFeお
よび不可避的不純物よりなることを特徴とする鍛造性と被削性に優れた鋼。
(3)質量%で、
C :0.1〜0.85%、
Si:0.01〜1.5%、
Mn:0.05〜2.0%、
P :0.003〜0.2%、
S :0.003〜0.5%、
Zr:0.0003〜0.01%
を含有するとともに
Al:0.01%以下、
total−O:0.02%以下、
total−N:0.02%以下
に制限し、さらに、
Cr:0.01〜2.0%、
Ni:0.05〜2.0%、
Mo:0.05〜1.0%
のうち1種または2種以上を含み、かつ、MnSの平均アスペクト比10以下で
、最大アスペクト比30以下を有し、残部がFeおよび不可避的不純物よりなる
ことを特徴とする鋼。
(4)質量%で、
C :0.1〜0.85%、
Si:0.01〜1.5%、
Mn:0.05〜2.0%、
P :0.003〜0.2%、
S :0.003〜0.5%、
Zr:0.0003〜0.01%
を含有するとともに
Al:0.01%以下、
total−O:0.02%以下、
total−N:0.02%以下
に制限し、さらに、
Cr:0.01〜2.0%、
Ni:0.05〜2.0%、
Mo:0.05〜1.0%
のうち1種または2種以上を含み、かつ、MnSの平均アスペクト比10以下で
、最大アスペクト比30以下を有し、更に、最大MnS粒径(μm)が110×
〔S%〕−15以下、1mm2あたりのMnS数が3800×〔S%〕+150
以下を有し、残部がFeおよび不可避的不純物よりなることを特徴とする鍛造性
と被削性に優れた鋼。
(5)上記(1)〜(4)のいずれかに記載の鋼が、質量%で、
V :0.05〜1.0%、
Nb:0.005〜0.2%、
Ti:0.005〜0.1%
のうち少くとも1種以上を含み、残部がFeおよび不可避的不純物よりなること
を特徴とする鍛造性と被削性に優れた鋼。
(6)上記(1)〜(5)のいずれかに記載の鋼が、質量%で、
Ca:0.0002〜0.005%、
Mg:0.0003〜0.005%、
Te:0.0003〜0.005%
のうち1種または2種以上を含み、残部がFeおよび不可避的不純物よりなるこ
とを特徴とする鍛造性と被削性に優れた鋼。
(7)上記(1)〜(6)のいずれかに記載の鋼が、質量%で、
Bi:0.05〜0.5%、
Pb:0.01〜0.5%
のうちの1種または2種を含み、残部がFeおよび不可避的不純物よりなること
を特徴とする鍛造性と被削性に優れた鋼。
(8)上記(1)〜(7)のいずれかに記載の鋼が、質量%で、
B:0.0005%以上0.004%未満を含み、残部がFeおよび不可避的不
純物よりなることを特徴とする鍛造性と被削性に優れた鋼。
発明を実施するための最良の形態
先ず、本発明による鋼成分組成について説明する。
Cは鋼材の基本強度に大きな影響を及ぼす元素であり、十分な強度を得るため
に0.1〜0.85%とした。0.1%未満では十分な強度を得られず、他の合
金元素をさらに多量に投入せざるを得ず、0.85%を超えると過共析に近くな
り、硬質の炭化物を多く析出するので被削性を著しく低下させる。
Siは脱酸元素として添加されるが、フェライトの強化や焼戻し軟化抵抗を付
与するために添加する。本発明においては脱酸元素としても必要である。0.0
1%未満ではその効果は認められず、1.5%を超えると脆化し、高温での変形
抵抗も増加するのでこれを上限とした。
Mnは鋼中硫黄をMnSとして固定・分散させるために必要であるとともに、
マトリックスに固溶させて焼入れ性の向上や焼入れ後の強度を確保するために必
要である。その下限値は0.05%で、それ未満であるとSがFeSとなり脆く
なる。Mn量が大きくなると素地の硬さが大きくなり冷間加工性が低下するとと
もに、強度や焼入れ性に及ぼす影響も飽和するので、2.0%を上限とした。
Pは鋼中において素地の硬さが大きくなり、冷間加工性だけでなく、熱間加工
性や鋳造特性が低下するので、その上限を0.2%にしなければならない。一方
、被削性に効果がある元素で下限値を0.003%とした。
SはMnと結合してMnS介在物として存在する。MnSは被削性を向上させ
るが、伸延したMnSは鍛造時の異方性を生じる原因の一つである。異方性の程
度と要求される被削性によって調整されるべきであるが、同時に熱間および冷間
鍛造における割れの原因となり易いので、その上限値を0.5%とした。下限は
現状の工業生産レベルでコストが大幅に上昇しない限界である0.003%とし
た。
Zrは脱酸元素であり、ZrO2またはZrを含む酸化物(以下Zr酸化物と
いう。)を生成する。酸化物はZrO2と考えられZrO2がMnSの析出核と
なるので、MnSの析出サイトを増やし、MnSを均一分散させる。またZrは
MnSに固溶して複合硫化物を生成してその変形能を低下させ、圧延や熱間鍛造
してもMnS形状の伸延を抑制する働きがある。したがって異方性の低減に有効
な元素である。0.0003%未満ではその効果は顕著ではなく、0.01%以
上添加しても歩留まりが極端に悪くなるばかりでなく、硬質のZrO2やZrS
などを大量に生成し、かえって被削性や衝撃値や疲労特性などの機械的性質を低
下させる。したがって成分範囲を0.0003〜0.01%と規定した。
これまでもZr添加によってMnSが球状化するとの知見はあったが、「鉄と
鋼」第62年(1976)7号p.893には、MnS−Zr3S4の共晶介在
物を生じるとMnSの変形能を低下させてMnSの伸延を抑制できること、それ
には0.07%Sに対して0.02%以上必要であることが記されている。この
ような知見はMnSの変形能を抑制するために複合硫化物を生成させることが重
要であり、そのために多量のZr添加を必要としていた。しかし、過剰なZrは
Zr系の窒化物および硫化物のような酸化物以外の硬質介在物およびそのクラス
ターを生成し、機械的性質と被削性を低下させる。つまり、多量Zr添加によっ
てMnS変形能を低下させるには硬質介在物とクラスターによる弊害を伴う。
一方、本発明は、MnSの変形能よりもMnSの析出核としてのZr系酸化物
の役割に注目した。そして、鋼中にMnSが微細に分散すれば、たとえMnSが
圧延や鍛造によって伸延されても鋼にとって致命的な欠陥にならないと考えて快
削鋼を開発してきた。検討の結果、0.01%以下のZr添加で生成されるZr
系酸化物は微細分散可能であるとともにMnSの析出核となり易いことを見出し
、それを積極的に利用することで、MnSを微細分散した機械的性質と被削性に
優れた鋼を開発した。
本発明では、Zrは酸化物として単独または他の酸化物と複合して存在し、そ
の分布は微細分散し、鋼中でMnSの析出核になり易い。そしてMnSの析出核
としてのZr系酸化物を微細分散させるだけであれば、Sに対して過剰なZrを
添加する必要がないので、過剰Zrから生成されるZr系の窒化物および硫化物
のような酸化物以外の硬質介在物およびそのクラスターを生成せず、多量Zr添
加になる弊害、即ち衝撃値などの機械的性質や被削性の低下を伴わない。
Alは脱酸元素で鋼中ではAl2O3を形成する。Al2O3は硬質なので切
削時に工具損傷の原因となり、摩耗を促進させる。またAlを添加するとOが少
なくなり、Zr酸化物が生成しにくい。また微細なZrO2を均一分散させるた
めにもAlを添加しない方が良い。この影響はZrの添加量や歩留まり、そして
MnSの分布や形状に大きく影響し、本発明では硬質Al2O3の抑制とZr酸
化物を微細均一分散させるために0.01%以下に制限した。このことでZrの
添加量を大きく低減でき、Zr添加の析出核としての効果とMnSとの複合化効
果を大きくすることが出来る。
Oはfreeで存在する場合には冷却時に気泡となり、ピンホールの原因とな
る。またSi,Al,Zrなどと結合すると硬質酸化物を生成するため、制限が
必要である。本鋼ではZrの微細分散効果が無くなる0.02%を上限として制
限した。
Nは固溶Nの場合、鋼を硬化させる。特に切削においては動的ひずみ時効によ
って刃先近傍で硬化し、工具の寿命を低下させる。またTi,Al,Vなどの窒
化物として存在する場合もオーステナイト粒の成長を抑制するので制限が必要で
ある。特に高温域ではTiNやZrNを生成する。また窒化物を生成しない場合
でも鋳造途中に気泡を生成し、疵などの原因となる。本発明ではその弊害が顕著
になる0.02%を上限とした。
Crは焼入れ性向上、焼戻し軟化抵抗付与元素である。そのため高強度化が必
要な鋼には添加される。その場合、0.01%以上の添加を必要とする。しかし
多量に添加するとCr炭化物を生成し脆化させるため、2.0%を上限とした。
Niはフェライトを強化し、延性を向上させるとともに焼入れ性向上、耐食性
向上にも有効である。0.05%未満ではその効果は認められず、2.0%を超
えて添加しても、機械的性質の点では効果が飽和するので、これを上限とした。
Moは焼戻し軟化抵抗を付与するとともに、焼入れ性を向上させる元素である
。0.05%未満ではその効果が認められず、1.0%を超えて添加してもその
効果が飽和しているので、0.05〜1.0%を添加範囲とした。
Bは固溶している場合は粒界強化や焼入れ性に効果があり、析出する場合には
BNとして析出するので被削性に効果がある。これらの効果は0.0005%未
満では顕著でなく、0.004%以上添加してもその効果が飽和し、BNが多く
析出しすぎるとかえって鋼の機械的性質を損なう。そこで0.0005%以上0
.004%未満を範囲とした。
Vは炭窒化物を形成し、二次析出硬化により鋼を強化することが出来る。0.
05%以下では高強度化に効果はなく、1.0%を超えて添加すると多くの炭窒
化物を析出し、かえって機械的性質を損なうので、これを上限とした。なお、V
の添加は0.2%超が好ましい。
V,Nb,Tiなどは鋼中で窒化物、炭化物、炭窒化物などを生成する。それ
らはピン止め粒子としてオーステナイト粒の成長を抑制するために、鍛造や熱処
理時に変態点以上に加熱した場合のオーステナイト粒径を制御する元素として用
いられることも多い。その析出温度はそれぞれ異なるが、工業的に実施されてい
る熱処理の温度制御の精度を考えると、極力広い温度域でピン止め効果を発揮し
てオーステナイト粒径を制御することが必要である。特に熱間鍛造では、形状に
より冷却温度が部材内の位置によっても大きく異なる。
Nb,Tiは比較的高温において析出物を生成するのに対して、Vはこれらよ
り低温において炭化物を析出するのでVを添加することが好ましいが、Vを単独
で添加する場合には、Vは0.2%超1.0%以下とすることにより効果が達成
できる。また、VとNb,Tiのいずれかまたは両方を併用することでピン止め
粒子として最適な寸法の析出物を均一に鋼中に分散させることが出来る。
このような数種の元素を併用する場合には、単独添加の場合より添加量を抑制
してもオーステナイト粒径を制御することが出来、Vの下限は0.05%の添加
でも効果が認められるようになる。
したがって、Nb,Tiの1種または2種をVと同時に添加する場合のVの下
限は0.05%とした。
Nbも炭窒化物を形成し、二次析出硬化により鋼を強化することが出来る。0
.005%以下では高強度化に効果はなく、0.2%を超えて添加すると多くの
炭窒化物を析出し、かえって機械的性質を損なうので、これを上限とした。
Tiも炭窒化物を形成し、鋼を強化する。また脱酸元素でもあり、軟質酸化物
を形成させることで被削性を向上させることが可能である。0.005%以下で
はその効果が認められず、0.1%を超えて添加してもその効果が飽和する。ま
たTiは高温でも窒化物となりオーステナイト粒の成長を抑制する。そこで上限
を0.1%とした。
Caは脱酸元素であり、軟質酸化物を生成し、被削性を向上させるだけでなく
、MnSに固溶してその変形能を低下させ、圧延や熱間鍛造してもMnS形状の
伸延を抑制する働きがある。したがって異方性の低減に有効な元素である。0.
0002%未満ではその効果は顕著ではなく、0.005%を超えて添加しても
歩留まりが極端に悪くなるばかりでなく、硬質のCaOを大量に生成し、かえっ
て被削性を低下させる。したがって成分範囲を0.0002〜0.005%と規
定した。
Mgは脱酸元素であり、酸化物を生成する。酸化物はMnSの析出核になりM
nSの微細均一分散に効果がある。したがって異方性の低減に有効な元素である
。0.0003%未満ではその効果は顕著ではなく、0.005%を超えて添加
しても歩留まりが極端に悪くなるばかりで効果は飽和する。したがって成分範囲
を0.0003〜0.005%と規定した。
Teは被削性向上元素である。またMnTeを生成したり、MnSと共存する
ことでMnSの変形能を低下させてMnS形状の伸延を抑制する働きがある。し
たがって異方性の低減に有効な元素である。この効果は0.0003%未満では
認められず、0.005%を超えると鋳造時の割れの原因となり易い。
BiおよびPbは被削性向上に効果のある元素である。その効果は0.05%
未満では認められず、0.5%を超えて添加しても被削性向上効果が飽和するだ
けでなく、熱間鋳造特性が低下して疵の原因となり易い。
次に、本発明においては上述した成分組成に加え、MnSの平均アスペクト比
、および最大アスペクト比、また、最大MnS粒径、単位面積(1mm2)あた
りのMnS数が重要な要素であり、MnSの平均アスペクト比は10以下、最大
アスペクト比は30以下、最大MnS粒径(μm)は110×〔S%〕+15以
下、1mm2あたりのMnS数は3800×〔S%〕+150以下とする必要が
ある。
平均アスペクト比10以下、最大アスペクト比30以下とする理由は、図8(
a)、図9に示すように、アスペクト比は初期MnS粒径が大きくなれば、アス
ペクト比も大きくなる傾向にある。実施例にもあるようにアスペクト比が大きい
と、材質の異方性が助長され、断面方向の衝撃値が疲労強度を低下させることに
なる。また鍛造においてはさまざまな変形を加えられるため、伸延されたMnS
は破壊起点となることが多い。したがってMnSの平均アスペクト比<20以上
ではこの伸延されたMnSによる破壊特性の劣化が顕著になる。またMnSの最
大アスペクト比に関しても30を超えるとMnSによる破壊特性の劣化が顕著に
なる。
また、最大MnS粒径(μm)110×〔S%〕+15以下、1mm2あたり
のMnS数3800×〔S%〕+150以下とする理由は以下の理由に基づくも
のである。MnSは応力集中源となるため破壊起点となりやすいことが知られて
おり、特にその大きさの影響が強い。一方、被削性はS量に比例して向上するも
のの、それほどMnSの大きさの影響は顕著ではないことをみいだした。そのた
め、同一S量の鋼で比較するとMnSは小さく多数分散した鋼は大きく少数分散
した鋼より被削性は同等でも破壊特性や鍛造性は優れる。その効果はS量の影響
を受けるが、図8(a)、図9に示すように、最大MnS粒径(μm)<110
×〔S%〕+15かつ1mm2あたりのMnS数>3800×〔S%〕+150
であれば鍛造特性と破壊特性の劣化を最小限に抑制しつつ、S添加量相当の被削
性を確保できることを見出した。逆に最大MnS粒径(μm)>110×(S%
〕+15あるいは1mm2あたりのMnS数<3800×〔S%〕+150であ
ると破壊特性や鍛造性に劣る。
画像処理装置によってMnS系介在物を抽出し、それぞれのMnSに関して以
下の項目を算出する。画像処理装置では光学的取り込まれた像をCCDカメラに
よってデジタル化するのでMnSの大きさ、占有面積などが測定可能である。測
定視野は倍率500倍で、1視野9000μm2として50視野を繰返し測定す
る。この測定の対象は、円相当径(R)、圧延方向長さ(L)、半径方向厚さ(
H)、アスペクト比(L/H)である。個々のMnSに関するこれら測定値の最
大値および平均値を算出することが可能で、平均アスペクト比とは個々のMnS
のアスペクト比の平均値であり、測定された個々のアスペクト比の中で最大のも
のを最大アスペクト比と記す。
また、MnSの粒径に関しては、画像処理装置にて測定し、MnSの測定面積
を円にした場合の直径、いわゆる円相当径であり、1mm2あたりのMnS数と
は測定面積に含まれたMnS数を測定面積で除した値である。
実施例
本発明の効果を実施例によって説明する。表1に示す供試材は2t真空溶解炉
で溶製後、ビレットに分解圧延、さらにφ60mmに圧延した。圧延後、熱間加
工性評価用熱間据え込み試験片、冷間加工評価用冷間据え込み試験片を切り出し
て据え込み試験を行った。また一部は熱処理として1200℃に加熱後、放冷し
て切削試験に供した。
ここで鋼中Zrの分析方法であるが、JIS G 1237−1997付属書
3と同様の方法でサンプルを処理した後、鋼中Nb量と同様に鋼中Zr量をIC
P(誘導結合プラズマ発光分光分析法)によって測定した。ただし、本発明での
実施例の測定に供したサンプルは2g/鋼種で、ICPにおける検量線も微量Z
rに適するように設定して測定した。即ち、Zr濃度が1〜200ppmとなる
ようにZr標準液を希釈して異なるZr濃度の溶液を作成し、そのZr量を測定
することで検量線を作成した。なお、これらのICPに関する共通的な方法につ
いては、JIS K 0116−1995(発光分光分析方法通則)およびJI
S Z 8002−1991(分析、試験の許容差通則)による。
図1は鍛造加工性(熱間、冷間)評価用試験片切り出し位置と試験片形状を説
明するための図である。図1(a)の切り出し位置1で、据え込み試験片の切り
出し方向は、鋼中MnS2が長手方向になるように図1(b)、図1(c)に示
す熱間据え込み試験片3およびノッチ5を設けた冷間据え込み試験片4を切り出
した。
図2は据え込み試験での割れ発生位置を説明する図である。据え込み試験では
図2に示すように荷重6の負荷をかけて試験片が変形7すると外周部に周方向に
引張応力が生じる。その際、多くの場合、鋼中のMnSが破壊源となり割れ8を
生じる場合が多い。このように切り出した試験片の据え込み試験により、鍛造時
の加工性を評価できる。
熱間における据え込み試験片はφ20mm×30mmで熱電対を取り付けてあ
り、高周波により1000℃まで加熱し、3s以内に据え込み鍛造を行った。さ
まざまなひずみで鍛造し、図3に示すように、試験片の変形前9および変形後1
0の割れの発生するひずみを限界ひずみとして測定した。ここでひずみとは式(
1)で定義される、いわゆる公称ひずみである。
ε=(Ho−H)/Ho 式(1)
ここでε:ひずみ、Ho:変形前の試験片高さ、H:変形後の試験片高さを意味
する。
表1に加工性を評価した実施例を示す。表1実施例1〜5はS45Cをベース
とした鋼でS量を変化させている。その比較例として実施例6〜10はZrを添
加していない鋼である。また実施例(比較例)11および12はAl量多量添加
かつZr無添加でPbを添加したもの、実施例(比較例)13および14はZr
を添加しているものの、Al量を多量添加してS量を変化させてある。実施例1
5はAl多量添加し、Zrを無添加の比較例である。同一のS量で比較すると、
Pbを添加した実施例11,12は熱間鍛造性に劣る。またS量が多くなると、
Zrを添加した発明例2〜5は比較例7〜10より優れる。さらにS量が多い場
合にはZrの有無に関わらず、Al量が多いと実施例14,15のように熱間加
工性か発明例より劣った。
図4は表1の実施例に関して熱間鍛造性に及ぼすS量の影響を示す図である。
また冷間加工性を評価するために冷間据え込み試験を行った。図1のように切
り出した素材を850℃から焼き入れた後、700℃で12hrの球状化焼鈍し
た。その後、機械加工で2mmのノッチ付φ7mm×14mm冷間据え込み試験
片を作成した。図5は実施例1〜15の冷間加工における限界ひずみ測定結果で
ある。ひずみの定義は式1と同様である。
同様に表2にS45CにVを添加し、オーステナイト粒径を微細化するととも
に、強度を向上させた実施例を示す。図6に表2の実施例の1000℃における
熱間鍛造性評価結果を示す。この場合にもS量が増加すれば熱間鍛造性が低下し
ているが、同一S量で比較すると実施例17〜20(発明例)は実施例22〜2
5(比較例)より良好な熱間鍛造性を示した。
表1に示した実施例について被削性を評価した結果を図7に示す。被削性評価
はドリル穿孔試験で行い、表3にその切削条件を示す。累積穴深さ1000mm
まで切削可能な最高の切削速度(いわゆるVL1000)で被削性を評価した。
図7に示すようにS量が多くなると被削性が向上する。しかし同一S量で比較
するとAlを多量に添加した場合(実施例13〜15)はAlを規定内に制限し
た場合より被削性が劣る。Alが規定内の場合、Zrの有無で比較すると、いず
れのS量においても同等の被削性である。またPbを添加した実施例11,12
と比較すると、実施例2と11が同等の被削性であるが、図4に示すように熱間
加工性は実施例2の方が優れた。同様に実施例3と12の比較では同等の被削性
にもかかわらず実施例3(発明例)の方が熱間加工性が優れた。このように本発
明は熱間加工性と被削性を両立するのに有効である。
同様の効果はVを添加して高強度化した場合でも見られ、表2に被削性を評価
した結果を数値で示したが、同一S量で比較した場合には発明例は比較例と同様
の被削性であった。したがって、本発明を用いれば高強度化しても鍛造性と被削
性の両立が達成できる。
表4にZr量を変化させた実施例を示す。表4の実施例に実施例2および3を
加え、機械的性質とZr量の関係を検討した。図8(a)にZr量の衝撃値、硫
化物アスペクト比および硫化物の単位面積当たりの個数を示す。衝撃試験片の切
り出しかたは図8(b)にあるとおりで、長手方向に切り出す場合をL、断面方
向に切り出す場合をCとした。Zrを添加しない場合、圧延長手方向の衝撃値は
優れるものの、断面方向の衝撃値は極めて低い。S量が多くなるとその傾向がよ
り顕著になる。しかしZrを添加すると長手方向の衝撃値がわずかに低下するも
のの、断面方向は大きく向上する。その原因は硫化物の微細分散とアスペクト比
の改善によるものと考えられる。特に硫化物数が増加し、微細に分散するとたと
えアスペクト比の大きな硫化物が含まれていても寸法が小さいために機械的性質
への影響も小さくなると考えられる。
さらに表5にAl量を変化させた実施例を示す。Al量が増加すると被削性が
低下することは既に述べたが、Al量の効果を明確にするため、表5の実施例に
実施例2および27を加え、硫化物形状に及ぼすAl量の影響を図9に示す。Z
rを微量添加した場合にはAl量が0.01%を超えると硫化物数が減少すると
ともに、アスペクト比が増加した。この場合、熱間据え込み試験における限界ひ
ずみが低下する。またAlの増加とともに被削性AL1000が明らかに低下す
る。このため本発明ではAlを0.01%以下に規定した。
表6に他の元素への影響を検討した実施例を示す。その製造方法と熱間加工性
および被削性評価方法は表1に示す実施例と同様である。表6、表6−1、表6
−2、表6−3は、実施Nos.41〜72においてさまざまな合成元素を添加
した場合の熱間限界ひずみと被削性を示したものである。これらの表における各
比較例は被削性の差は小さくとも熱間限界ひずみの点で大きく劣った。また、こ
れらの表における実施Nos.73〜78に示すような基本的な強度をC量によ
って変化させた場合にも発明例は比較例より優れる。表6−1、表6−3におけ
る実施Nos.79,80はそれぞれtotal−O量とtotal−N量を発
明の範囲外にした比較例である。これらは実施No.2と比較すると、熱間限界
ひずみと被削性の両面で劣った。このように本発明に含まれる実施例は同一のS
量で比較した場合、良好な熱間加工性と被削性を両立していることがわかる。
図10は、被削性への弊害をドリル工具寿命の指標であるVL1000(10
00mmの累積孔深さを穿孔可能な最大切削速度)にて評価した結果である。Z
rを多量に添加すると被削性が低下していることがわかる。また、図8の衝撃値
においても過剰なZr添加はMnSのアスペクトに優れるものの、ZrNやZr
Sなどのクラスターを生じて衝撃値が低下していることがわかる。
なお、図4〜10において、図中の添字は実施例No.を示している。
産業上の利用可能性
以上のような内容により、熱間加工性、機械的性質、被削性を兼ね備えた鋼を
供することが出来る。特に本発明の技術は熱処理やミクロ組織などの影響を大き
く受けず、硫化物の形状制御を基本としているので、調質鋼や非調質鋼を区別す
る必要がない。また加工に関しても熱間鍛造だけでなく、冷間鍛造に対しても有
効で、鍛造加工性、機械的性質、被削性を必要とする広範囲な鋼に対して有効で
ある。
TECHNICAL FIELD The present invention relates to steels used in automobiles, general machinery, etc., and in particular to steels with excellent hot forging and machinability. BACKGROUND ART In recent years, while steels have become stronger, their workability has decreased, and therefore there is a growing need for steels that do not decrease forging or cutting efficiency. Until now, general measures for hot forging have been to reduce inclusions, add elements that increase high-temperature ductility, and reduce elements that inhibit high-temperature ductility. On the other hand, it is known that adding machinability-improving elements such as S and Pb is effective in improving machinability, but these elements that are effective in improving machinability also reduce high-temperature ductility, making it difficult to achieve both hot forging and machinability. Pb, B
Although it is believed that i improves machinability and has relatively little effect on forging, it is known to reduce high-temperature ductility. S improves machinability by forming inclusions that become soft in cutting environments, such as MnS, but the size of MnS is larger than particles such as Pb, making it more likely to become a source of stress concentration. When MnS is stretched, particularly through forging or rolling, it becomes anisotropic, becoming extremely weak in a specific direction. Furthermore, such anisotropy must be taken into consideration in design. Therefore, technology is needed to minimize the anisotropy of such free-machining elements. Furthermore, P is known to improve machinability, but it cannot be added in large amounts due to the tendency for cracks to form during hot casting, and there is a limit to its effectiveness in improving machinability. It has been claimed that the addition of Te eliminates anisotropy (see Japanese Patent Application Laid-Open No. 1975).
(5-41943), Te is prone to cracking during casting, rolling, and forging. Furthermore, a technology disclosed in JP 49-66522 A (1974-66522) aims to improve the machinability of steel over a wide range of cutting speeds, from low to high, by adding a deoxidizer containing Zr and Ca to the steel. However, this technology still does not solve the problem of fracture due to MnS elongated by rolling or forging. Therefore, further technological innovation is required to achieve both hot ductility and machinability. Disclosure of the Invention The present invention addresses the above-mentioned situation by providing a steel with excellent hot ductility and machinability. Generally, steel is processed by rolling or forging, and the plastic flow during this process causes anisotropy in its mechanical properties. During forging, cracking due to this anisotropy effectively indicates the forging limit. Therefore, to improve forgeability, it is effective to make the shape of inclusions such as MnS as spherical as possible and minimize anisotropy. Furthermore, even if anisotropy occurs, the influence of anisotropy can be reduced if the size of the inclusions is small. Therefore, it is desirable to use steel components that finely disperse MnS, which improves machinability, and maintain its spherical shape. The present invention is a steel with excellent forgeability and machinability, which was made based on the above findings,
The gist of the invention is as follows: (1) In mass %, the alloy contains C: 0.1 to 0.85%, Si: 0.01 to 1.5%, Mn: 0.05 to 2.0%, P: 0.003 to 0.2%, S: 0.003 to 0.5%, and Zr: 0.0003 to 0.01%, with Al being limited to 0.01% or less, total O being limited to 0.02% or less, and total N being limited to 0.02% or less, and the average aspect ratio of MnS being 10 or less and the maximum aspect ratio being 30 or less.
(2) A steel having excellent forgeability and machinability, characterized by containing, by mass%, C: 0.1 to 0.85%, Si: 0.01 to 1.5%, Mn: 0.05 to 2.0%, P: 0.003 to 0.2%, S: 0.003 to 0.5%, Zr: 0.0003 to 0.01%, and also containing Al: 0.01% or less, total-O: 0.02% or less, and total-N: 0.02% or less, and the average aspect ratio of MnS is 10 or less, and the maximum aspect ratio is 30.
and the maximum MnS particle size (μm) is 110×[S%]-15 or less, and
A steel having excellent forgeability and machinability, characterized in that the number of MnS per m2 is 3800 × [S%] - 150 or less, and the balance consisting of Fe and unavoidable impurities. (3) A steel containing, by mass%, C: 0.1 to 0.85%, Si: 0.01 to 1.5%, Mn: 0.05 to 2.0%, P: 0.003 to 0.2%, S: 0.003 to 0.5%, Zr: 0.0003 to 0.01%, with Al: 0.01% or less, total O: 0.02% or less, and total N: 0.02% or less, and further containing one or more of Cr: 0.01 to 2.0%, Ni: 0.05 to 2.0%, and Mo: 0.05 to 1.0%, and having an average aspect ratio of MnS of 10 or less and a maximum aspect ratio of 30 or less, with the balance being Fe and unavoidable impurities. (4) In mass%, it contains C: 0.1 to 0.85%, Si: 0.01 to 1.5%, Mn: 0.05 to 2.0%, P: 0.003 to 0.2%, S: 0.003 to 0.5%, Zr: 0.0003 to 0.01%, and is limited to Al: 0.01% or less, total-O: 0.02% or less, total-N: 0.02% or less, and further contains one or more of Cr: 0.01 to 2.0%, Ni: 0.05 to 2.0%, and Mo: 0.05 to 1.0%, and the average aspect ratio of MnS is 10 or less and the maximum aspect ratio is 30 or less, and further, the maximum MnS particle size (μm) is 110×
[S%] -15 or less, the number of MnS per mm2 is 3800 × [S%] + 150
(5) A steel having excellent forgeability and machinability, characterized in that the steel according to any one of (1) to (4) above contains, by mass, at least one of V: 0.05 to 1.0%, Nb: 0.005 to 0.2%, and Ti: 0.005 to 0.1%, with the balance consisting of Fe and unavoidable impurities. (6) A steel having excellent forgeability and machinability, characterized in that the steel according to any one of (1) to (5) above contains, by mass, one or more of Ca: 0.0002 to 0.005%, Mg: 0.0003 to 0.005%, and Te: 0.0003 to 0.005%, with the balance consisting of Fe and unavoidable impurities. (7) A steel with excellent forgeability and machinability, characterized in that the steel according to any one of (1) to (6) above contains, by mass, one or two of Bi: 0.05 to 0.5%, Pb: 0.01 to 0.5%, and the balance consisting of Fe and unavoidable impurities. (8) A steel with excellent forgeability and machinability, characterized in that the steel according to any one of (1) to (7) above contains, by mass, B: 0.0005% or more but less than 0.004%, and the balance consisting of Fe and unavoidable impurities. Best Mode for Carrying Out the Invention First, the steel composition according to the present invention will be explained. C is an element that has a significant effect on the basic strength of the steel, and is set to 0.1 to 0.85% to obtain sufficient strength. If the content is less than 0.1%, sufficient strength cannot be obtained, necessitating the addition of larger amounts of other alloying elements. If the content exceeds 0.85%, the steel approaches hypereutectoid, causing the precipitation of large amounts of hard carbides, significantly reducing machinability. Silicon is added as a deoxidizing element to strengthen ferrite and to provide resistance to temper softening. In the present invention, silicon is also necessary as a deoxidizing element.
If the content is less than 1%, the effect is not observed, and if the content exceeds 1.5%, embrittlement occurs and deformation resistance at high temperatures increases, so this was set as the upper limit. Mn is necessary to fix and disperse sulfur in the steel as MnS, and
It is necessary to dissolve in the matrix to improve hardenability and ensure strength after quenching. The lower limit is 0.05%; below this limit, S becomes FeS, resulting in embrittlement. As the Mn content increases, the hardness of the matrix increases, reducing cold workability, and its effects on strength and hardenability saturate, so the upper limit is set at 2.0%. P increases the hardness of the matrix in steel, reducing not only cold workability but also hot workability and castability, so its upper limit must be set at 0.2%. On the other hand, S is an element that has an effect on machinability, so its lower limit is set at 0.003%. S combines with Mn to form MnS inclusions. MnS improves machinability, but elongated MnS is one of the causes of anisotropy during forging. While the content should be adjusted depending on the degree of anisotropy and the required machinability, its upper limit is set at 0.5% because it is prone to cracking during hot and cold forging. The lower limit was set at 0.003%, which is the limit at which costs do not rise significantly at the current industrial production level. Zr is a deoxidizing element and forms ZrO2 or oxides containing Zr (hereinafter referred to as Zr oxides). The oxide is considered to be ZrO2 , and ZrO2 acts as a nucleus for MnS precipitation, increasing the number of MnS precipitation sites and uniformly dispersing MnS. Zr also dissolves in MnS to form complex sulfides, reducing its deformability and suppressing the elongation of the MnS shape even during rolling or hot forging. Therefore, it is an effective element for reducing anisotropy. At less than 0.0003%, the effect is not significant, and adding 0.01% or more not only significantly reduces yield, but also increases the hardness of ZrO2 and ZrS.
This leads to the formation of large amounts of oxides such as Zn, which in turn reduces mechanical properties such as machinability, impact strength, and fatigue resistance. Therefore, the element range was specified as 0.0003 to 0.01%. It has been known that adding Zr causes MnS to become spheroidized. However, in "Iron and Steel," Vol. 7, 1976, p. 893, it was noted that the formation of MnS - Zr3S4 eutectic inclusions reduces the deformability of MnS and inhibits its elongation, and that a content of 0.02% or more is required for 0.07% S. This knowledge suggests that the formation of complex sulfides is important to inhibit the deformability of MnS, and therefore the addition of large amounts of Zr is necessary. However, excessive Zr generates hard inclusions and clusters other than oxides, such as Zr-based nitrides and sulfides, which degrade mechanical properties and machinability. In other words, reducing MnS deformability through the addition of large amounts of Zr is accompanied by the adverse effects of hard inclusions and clusters. On the other hand, the present inventors focused on the role of Zr-based oxides as nuclei for precipitation of MnS rather than the deformability of MnS. They developed free-cutting steel on the basis that if MnS is finely dispersed in steel, even if MnS is elongated by rolling or forging, it will not become a fatal defect in the steel. As a result of their investigation, they found that the Zr generated by adding 0.01% or less Zr
We discovered that Zr-based oxides can be finely dispersed and easily serve as nuclei for MnS precipitation. By actively utilizing this, we developed a steel with finely dispersed MnS, which has excellent mechanical properties and machinability. In this invention, Zr exists as an oxide alone or in combination with other oxides, and its distribution is finely dispersed, making it easy to serve as nuclei for MnS precipitation in the steel. Furthermore, simply finely dispersing Zr-based oxides as MnS nuclei does not require the addition of excess Zr relative to S. Therefore, excess Zr does not produce hard inclusions other than oxides, such as Zr-based nitrides and sulfides, and their clusters. This avoids the adverse effects of adding large amounts of Zr, namely, a decrease in mechanical properties such as impact value and machinability. Al is a deoxidizing element and forms Al2O3 in steel. Because Al2O3 is hard , it can cause tool damage and promote wear during cutting. Furthermore, the addition of Al reduces oxygen, making it difficult for Zr oxides to form. Furthermore , it is preferable not to add Al to achieve uniform dispersion of fine ZrO2 . This influence significantly affects the amount of Zr added, yield, and the distribution and shape of MnS. In this invention, the Zr content is limited to 0.01% or less to suppress hard Al2O3 and to finely and uniformly disperse Zr oxide. This significantly reduces the amount of Zr added, enhancing the effect of Zr as a precipitation nucleus and its compounding effect with MnS. When free O is present, it forms bubbles during cooling, causing pinholes. Furthermore, when it combines with Si, Al, Zr, etc., it forms hard oxides, so it is necessary to limit its content. In this steel, the upper limit is set at 0.02%, at which point the fine dispersion effect of Zr is lost. When N is dissolved, it hardens the steel. In particular, during cutting, it hardens near the cutting edge due to dynamic strain aging, shortening tool life. Furthermore, when present as nitrides of Ti, Al, V, etc., it suppresses austenite grain growth, so it must be limited. TiN and ZrN form, especially at high temperatures. Even when nitrides are not formed, bubbles form during casting, causing defects. In the present invention, the upper limit is set at 0.02%, at which point the adverse effects become significant. Cr is an element that improves hardenability and imparts temper softening resistance. Therefore, it is added to steels that require high strength. In such cases, an addition of 0.01% or more is necessary. However, adding large amounts generates Cr carbides and causes embrittlement, so the upper limit is set at 2.0%. Ni strengthens ferrite, improves ductility, and is effective in improving hardenability and corrosion resistance. This effect is not observed at less than 0.05%, and the effect saturates at more than 2.0%, so this is the upper limit. Mo is an element that imparts temper softening resistance and improves hardenability. This effect is not observed at less than 0.05%, and the effect saturates at more than 1.0%, so the addition range is set at 0.05 to 1.0%. B is effective in strengthening grain boundaries and hardenability when dissolved, and precipitates as BN, which improves machinability. These effects are not significant when added in an amount of less than 0.0005%, and the effects are saturated when added in an amount of 0.004% or more. If too much BN precipitates, the mechanical properties of the steel are impaired.
The range is set to less than 0.004%. V forms carbonitrides and can strengthen steel through secondary precipitation hardening.
If V is added in an amount of 0.05% or less, there is no effect in increasing strength, and if V is added in an amount of more than 1.0%, a large amount of carbonitrides precipitates, which impairs the mechanical properties.
The addition of V is preferably more than 0.2%. Elements such as V, Nb, and Ti form nitrides, carbides, and carbonitrides in steel. They are often used as pinning particles to suppress austenite grain growth and control the austenite grain size when heated above the transformation point during forging or heat treatment. Although their precipitation temperatures vary, considering the precision of temperature control in industrially performed heat treatments, it is necessary to exert the pinning effect over as wide a temperature range as possible to control the austenite grain size. In particular, in hot forging, the cooling temperature varies significantly depending on the shape and position within the part. While Nb and Ti form precipitates at relatively high temperatures, V precipitates carbides at lower temperatures. Therefore, adding V is preferred. However, when adding V alone, the effect can be achieved by limiting the V content to more than 0.2% and not more than 1.0%. Furthermore, by using V in combination with either or both Nb and Ti, precipitates of optimal size as pinning particles can be uniformly dispersed in steel. When several elements are used in combination, the austenite grain size can be controlled even with a smaller amount of addition than when each element is added alone, and the effect can be seen even with a lower limit of 0.05% V. Therefore, when one or both of Nb and Ti are added simultaneously with V, the lower limit of V is set at 0.05%. Nb also forms carbonitrides and can strengthen steel through secondary precipitation hardening.
Below 0.005%, there is no effect on increasing strength, and above 0.2%, many carbonitrides precipitate, impairing mechanical properties, so this upper limit was set. Ti also forms carbonitrides and strengthens steel. It is also a deoxidizing element, and can improve machinability by forming soft oxides. Below 0.005%, this effect is not observed, and even if added above 0.1%, the effect saturates. Ti also forms nitrides even at high temperatures, suppressing the growth of austenite grains. Therefore, the upper limit was set at 0.1%. Ca is a deoxidizing element that not only forms soft oxides and improves machinability, but also dissolves in MnS, reducing its deformability and suppressing the elongation of the MnS shape during rolling and hot forging. Therefore, it is an effective element for reducing anisotropy. 0.
If the content is less than 0.002%, the effect is not significant, and if it exceeds 0.005%, not only does the yield deteriorate significantly, but a large amount of hard CaO is formed, which actually reduces machinability. Therefore, the component range is specified as 0.0002 to 0.005%. Mg is a deoxidizing element and forms oxides. The oxides act as nuclei for the precipitation of MnS, and M
Te is effective in finely and uniformly dispersing nS. Therefore, it is an effective element in reducing anisotropy. If it is added less than 0.0003%, the effect is not significant, and if it is added more than 0.005%, the yield will be extremely poor and the effect will saturate. Therefore, the component range is specified as 0.0003 to 0.005%. Te is an element that improves machinability. It also produces MnTe and, by coexisting with MnS, reduces the deformability of MnS and inhibits the elongation of the MnS shape. Therefore, it is an effective element in reducing anisotropy. This effect is not observed if it is less than 0.0003%, and if it exceeds 0.005%, it is likely to cause cracks during casting. Bi and Pb are elements that are effective in improving machinability. This effect is not observed if it is added less than 0.0003%, and if it is added more than 0.005%, it is likely to cause cracks during casting.
If the content is less than 0.5%, this is not observed, and if added in excess of 0.5%, not only does the effect of improving machinability saturate, but hot casting properties deteriorate, making it more likely to cause defects. Next, in the present invention, in addition to the above-mentioned composition, the average aspect ratio and maximum aspect ratio of MnS, as well as the maximum MnS grain size and the number of MnS per unit area (1 mm 2 ) are important factors, and it is necessary for the average aspect ratio of MnS to be 10 or less, the maximum aspect ratio to be 30 or less, the maximum MnS grain size (μm) to be 110×[S%]+15 or less, and the number of MnS per 1 mm 2 to be 3800×[S%]+150 or less. The reason for specifying the average aspect ratio to be 10 or less and the maximum aspect ratio to be 30 or less is as shown in FIG. 8 (
As shown in Figure 9, the aspect ratio tends to increase as the initial MnS grain size increases. As shown in the examples, a large aspect ratio promotes anisotropy of the material, which reduces the fatigue strength of the impact value in the cross-sectional direction. In addition, various deformations are applied during forging, so the elongated MnS
These often become fracture initiation sites. Therefore, when the average aspect ratio of MnS is less than 20 or more, the degradation of fracture properties due to elongated MnS becomes significant. Furthermore, when the maximum aspect ratio of MnS exceeds 30, the degradation of fracture properties due to MnS becomes significant. The reason for limiting the maximum MnS particle size (μm) to 110 × [S%] + 15 or less and the number of MnS particles per mm2 to 3800 × [S%] + 150 or less is as follows: MnS is known to be a stress concentration source and therefore prone to become fracture initiation sites, and its size has a particularly strong effect. On the other hand, while machinability improves in proportion to the S content, we found that the effect of MnS size is not as significant. Therefore, when comparing steels with the same S content, steels with small, highly dispersed MnS particles have superior fracture properties and forgeability to steels with large, less dispersed MnS particles, even if they have equivalent machinability. The effect is affected by the amount of S, but as shown in Figures 8(a) and 9, when the maximum MnS particle size (μm) is less than 110
× [S%] + 15 and the number of MnS per 1 mm2 > 3800 × [S%] + 150
It was found that if the MnS content is less than 110×(S%), the deterioration of forgeability and fracture properties can be minimized while ensuring machinability equivalent to the amount of added S.
] + 15 or the number of MnS per mm2 < 3800 × [S%] + 150, the fracture properties and forgeability are inferior. MnS-based inclusions are extracted using an image processing device, and the following items are calculated for each MnS. The image processing device digitizes the optically captured image using a CCD camera, making it possible to measure the size and occupied area of MnS. The measurement field is 500x magnification, and 50 fields are repeatedly measured, with each field being 9000 μm2 . The objects of this measurement are the circle equivalent diameter (R), rolling direction length (L), and radial thickness (
The maximum and average values of these measurements for individual MnS can be calculated, and the average aspect ratio is the average aspect ratio of the individual MnS.
The aspect ratio is the average value of the aspect ratios of the measured individual aspect ratios, and the largest aspect ratio among the individual measured aspect ratios is referred to as the maximum aspect ratio. Furthermore, the particle size of MnS was measured using an image processing device, and the diameter when the measured area of MnS is converted into a circle, i.e., the so-called circle equivalent diameter. The number of MnS per mm2 is the value obtained by dividing the number of MnS contained in the measured area by the measured area. Examples The effects of the present invention will be explained using examples. The test materials shown in Table 1 were melted in a 2-ton vacuum melting furnace, disassembled and rolled into billets, and further rolled to a diameter of 60 mm. After rolling, hot upset test pieces for evaluating hot workability and cold upset test pieces for evaluating cold workability were cut out and subjected to upset tests. Furthermore, some were heat-treated by heating to 1200°C, then allowed to cool, and then subjected to cutting tests. Regarding the method for analyzing Zr in steel, samples were treated in the same manner as in JIS G 1237-1997 Appendix 3, and the Zr content in the steel was measured using IC
The measurement was performed by inductively coupled plasma atomic emission spectroscopy (ICP). However, the sample used for the measurement in the examples of the present invention was 2 g per steel type, and the calibration curve for ICP was also based on a trace amount of Z
The measurement was performed by setting the Zr standard solution to be suitable for the Zr concentration. That is, the Zr standard solution was diluted to prepare solutions with different Zr concentrations so that the Zr concentration was 1 to 200 ppm, and the Zr amount was measured to prepare a calibration curve. The common method for these ICPs is described in JIS K 0116-1995 (General rules for optical emission spectroscopy analysis) and JIS K 0116-1995.
The test specimens were cut from the cutting position 1 shown in Figure 1(a) and the cutting direction of the upset test specimens was such that the MnS2 in the steel was aligned longitudinally. The hot upset test specimen 3 and the cold upset test specimen 4 with a notch 5 shown in Figures 1(b) and 1(c) were cut from the cutting position 1 shown in Figure 1(a) and the cutting direction of the upset test specimens was such that the MnS2 in the steel was aligned longitudinally. Figure 2 is a diagram illustrating the location of cracks occurring during the upset test. In the upset test, as shown in Figure 2, when a load 6 is applied to the test specimen, deformation 7 occurs at the outer periphery, generating circumferential tensile stress. In many cases, MnS in the steel acts as a fracture source, resulting in cracks 8. Upset tests of test specimens cut in this manner can be used to evaluate forging workability. The hot upsetting test specimens were φ20 mm x 30 mm and equipped with thermocouples. They were heated to 1000°C by high frequency and upset forged within 3 seconds. Forging was performed with various strains, and as shown in Figure 3, the specimens were measured 9 mm before deformation and 1 mm after deformation.
The strain at which cracking of 0 occurs was measured as the limit strain.
1), which is the so-called nominal strain. ε = (H o -H)/H o Formula (1) where ε is strain, H o is the height of the test piece before deformation, and H is the height of the test piece after deformation. Table 1 shows examples in which workability was evaluated. Table 1 Examples 1 to 5 are steels based on S45C, with varying amounts of S. As comparative examples, Examples 6 to 10 are steels to which no Zr has been added. Examples (comparative examples) 11 and 12 are steels to which a large amount of Al has been added, no Zr has been added, and Pb has been added. Examples (comparative examples) 13 and 14 are steels to which Zr has been added.
Although a large amount of Al was added, the amount of S was changed.
No. 5 is a comparative example in which a large amount of Al was added and no Zr was added.
Examples 11 and 12, in which Pb was added, were inferior in hot forgeability.
Inventive Examples 2 to 5, in which Zr was added, were superior to Comparative Examples 7 to 10. Furthermore, when the amount of S was large, regardless of the presence or absence of Zr, when the amount of Al was large, the hot workability was inferior to that of the inventive examples, as in Examples 14 and 15. Figure 4 shows the effect of S content on hot forgeability for the examples in Table 1. A cold upsetting test was also conducted to evaluate cold workability. The material cut out as shown in Figure 1 was quenched from 850°C and then spheroidized at 700°C for 12 hours. Then, cold upsetting test pieces with a 2mm notch and a diameter of 7mm x 14mm were machined. Figure 5 shows the results of limit strain measurement during cold working for Examples 1 to 15. The definition of strain is the same as in Equation 1. Similarly, Table 2 shows an example in which V was added to S45C to refine the austenite grain size and improve strength. Figure 6 shows the results of hot forgeability evaluation at 1000°C for the examples in Table 2. In this case, too, increasing the S content reduced hot forgeability, but when compared at the same S content, Examples 17 to 20 (inventive examples) showed significantly better results than Examples 22 to 24.
5 (comparative example) showed better hot forgeability. The results of evaluating the machinability of the Examples shown in Table 1 are shown in Figure 7. The machinability evaluation was carried out by a drilling test, and the cutting conditions are shown in Table 3. Cumulative hole depth 1000 mm
Machinability was evaluated at the highest cutting speed possible (so-called VL1000). As shown in Figure 7, the machinability improves as the S content increases. However, when comparing at the same S content, when a large amount of Al is added (Examples 13 to 15), the machinability is inferior to when the Al content is limited to the specified range. When the Al content is within the specified range, and when comparing with and without Zr, the machinability is equivalent regardless of the S content. Also, Examples 11 and 12, which added Pb,
In comparison, Examples 2 and 11 had comparable machinability, but Example 2 had superior hot workability, as shown in Figure 4. Similarly, in a comparison of Examples 3 and 12, despite comparable machinability, Example 3 (invention example) had superior hot workability. Thus, the present invention is effective in achieving both hot workability and machinability. A similar effect was observed when increasing strength by adding V. Table 2 shows the numerical results of machinability evaluation. When compared at the same S content, the invention example had similar machinability to the comparative example. Therefore, by using the present invention, both forgeability and machinability can be achieved even with high strength. Table 4 shows examples in which the Zr content was varied. Examples 2 and 3 were added to the examples in Table 4 to examine the relationship between mechanical properties and Zr content. Figure 8(a) shows the impact value, sulfide aspect ratio, and number of sulfides per unit area for each Zr content. The impact test specimens were cut as shown in Figure 8(b), with L representing the longitudinal cut and C representing the cross-sectional cut. When Zr is not added, the impact value in the longitudinal direction of rolling is excellent, but the impact value in the cross-sectional direction is extremely low. This tendency becomes more pronounced as the amount of S increases. However, when Zr is added, the impact value in the longitudinal direction decreases slightly, but the impact value in the cross-sectional direction improves significantly. This is thought to be due to the fine dispersion of sulfides and the improvement of the aspect ratio. In particular, when the number of sulfides increases and they are finely dispersed, even if sulfides with a large aspect ratio are included, their small size is thought to reduce the effect on mechanical properties. Furthermore, Table 5 shows examples in which the Al content was changed. As already mentioned, an increase in the Al content reduces machinability. In order to clarify the effect of the Al content, Examples 2 and 27 were added to the examples in Table 5, and the effect of the Al content on the sulfide shape is shown in Figure 9.
When trace amounts of r were added, the number of sulfides decreased and the aspect ratio increased when the Al content exceeded 0.01%. In this case, the limiting strain in the hot upsetting test decreased. Furthermore, the machinability AL1000 clearly decreased with increasing Al content. For this reason, the Al content was specified to be 0.01% or less in this invention. Table 6 shows examples in which the effects of other elements were investigated. The manufacturing method and the methods for evaluating hot workability and machinability were the same as those of the examples shown in Table 1. Table 6, Table 6-1, Table 6
Tables 6-2 and 6-3 show the hot limit strain and machinability of Example Nos. 41 to 72 when various synthetic elements are added. Although the differences in machinability are small, the comparative examples in these tables are significantly inferior in terms of hot limit strain. Furthermore, when the basic strength is changed by the amount of C, as shown in Example Nos. 73 to 78 in these tables, the invention examples are also superior to the comparative examples. Example Nos. 79 and 80 in Tables 6-1 and 6-3 are comparative examples in which the total O and total N amounts are outside the ranges of the invention. Compared to Example No. 2, these were inferior in both hot limit strain and machinability. Thus, the examples included in the present invention are comparative examples in which the same S content is used.
When compared by amount, it can be seen that good hot workability and machinability are both achieved. FIG. 10 shows the adverse effect on machinability as a function of VL1000 (10
The cumulative hole depth of 1000 mm was evaluated at the maximum cutting speed at which drilling was possible.
It can be seen that the addition of a large amount of Zr reduces the machinability. Also, in the impact values shown in Figure 8, the addition of excessive Zr results in an excellent aspect ratio of MnS, but the addition of ZrN and Zr
It can be seen that clusters of sulfur and other elements are formed, resulting in a decrease in impact value. In Figures 4 to 10, the subscripts in the figures indicate Example Nos. Industrial Applicability Based on the above, it is possible to provide steels that combine hot workability, mechanical properties, and machinability. In particular, the technology of the present invention is not significantly affected by heat treatment or microstructure, and is based on shape control of sulfides, so there is no need to distinguish between tempered and non-tempered steels. Furthermore, with regard to processing, the technology is effective not only for hot forging but also for cold forging, and is effective for a wide range of steels that require forgeability, mechanical properties, and machinability.
図1(a),図1(b),図1(c)は、鍛造加工性(熱間、冷間)評価用試
験片切り出し位置と試験片形状を説明するための図である。
図2は、据え込み試験での割れ発生位置を説明する図である。
図3は、鍛造加工性評価(据え込み試験)時のひずみの定義を説明する図であ
る。
図4は、表1の実施例に関して熱間鍛造性に及ぼすS量の影響を示す図である
。
図5は、表1の実施例に関して冷間鍛造性に及ぼすS量の影響を示す図である
。
図6は、表2の実施例に関して熱間加工性に及ぼすS量の影響を示す図である
。
図7は、表1の実施例に関して被削性に及ぼすS量の影響を示す図である。
図8(a)は、衝撃値、硫化物形状および硫化物数に及ぼすZr量の影響を示
す図で、図8(b)は試験片採取位置を示す図である。
図9は、硫化物形状、数、熱間鍛造性および被削性に及ぼすAl添加量の影響
を示す図である。
図10は、工具寿命に及ぼすZr量の影響を示す図である。
Figures 1(a), 1(b), and 1(c) are diagrams illustrating the cutting positions and test specimen shapes for evaluating forgeability (hot and cold). Figure 2 is a diagram illustrating the location of cracks during an upsetting test. Figure 3 is a diagram illustrating the definition of strain during forgeability evaluation (upsetting test). Figure 4 is a diagram illustrating the effect of S content on hot forgeability for the Examples in Table 1. Figure 5 is a diagram illustrating the effect of S content on cold forgeability for the Examples in Table 1. Figure 6 is a diagram illustrating the effect of S content on hot workability for the Examples in Table 2. Figure 7 is a diagram illustrating the effect of S content on machinability for the Examples in Table 1. Figure 8(a) is a diagram illustrating the effect of Zr content on impact value, sulfide shape, and sulfide number, and Figure 8(b) is a diagram illustrating the test specimen cutting positions. Figure 9 is a diagram illustrating the effect of Al content on sulfide shape, number, hot forgeability, and machinability. Figure 10 is a diagram illustrating the effect of Zr content on tool life.
───────────────────────────────────────────────────── フロントページの続き (72)発明者 内藤 賢一郎 北海道室蘭市仲町12番地 新日本製鐵株式 会社 室蘭製鐵所内 (72)発明者 福安 憲次 東京都千代田区大手町二丁目6番3号 新 日本製鐵株式会社内 (注)この公表は、国際事務局(WIPO)により国際公開された公報を基に作 成したものである。 なおこの公表に係る日本語特許出願(日本語実用新案登録出願)の国際公開の 効果は、特許法第184条の10第1項(実用新案法第48条の13第2項)に より生ずるものであり、本掲載とは関係ありません。───────────────────────────────────────────────────── Continued from the front page (72) Inventor: Kenichiro Naito 12 Nakamachi, Muroran, Hokkaido, Japan Muroran Steel Works, Nippon Steel Corporation (72) Inventor: Kenji Fukuyasu 6-3 Otemachi 2-chome, Chiyoda-ku, Tokyo, Japan (Note) This publication is based on the publication published internationally by the International Bureau of Patents (WIPO). The effect of the international publication of the Japanese patent application (Japanese utility model registration application) related to this publication arises pursuant to Article 184-10, Paragraph 1 of the Patent Act (Article 48-13, Paragraph 2 of the Utility Model Act) and is unrelated to this publication.
Claims (8)
以下を有し、残部がFeおよび不可避的不純物よりなることを特徴とする鍛造性
と被削性に優れた鋼。Claim 1: A steel sheet containing, by mass%, C: 0.1 to 0.85%, Si: 0.01 to 1.5%, Mn: 0.05 to 2.0%, P: 0.003 to 0.2%, S: 0.003 to 0.5%, and Zr: 0.0003 to 0.01%, with Al being limited to 0.01% or less, total-O: 0.02% or less, and total-N: 0.02% or less, and with an average aspect ratio of MnS of 10 or less and a maximum aspect ratio of 30 or less.
A steel having excellent forgeability and machinability, characterized by having the following:
以下を有し、更に最大MnS粒径(μm)が110×〔S%〕+15以下、1m
m2あたりのMnS数が3800×〔S%〕+150以下を有し、残部がFeお
よび不可避的不純物よりなることを特徴とする鍛造性と被削性に優れた鋼。Claim 2: A steel sheet containing, by mass%, C: 0.1 to 0.85%, Si: 0.01 to 1.5%, Mn: 0.05 to 2.0%, P: 0.003 to 0.2%, S: 0.003 to 0.5%, and Zr: 0.0003 to 0.01%, with Al being limited to 0.01% or less, total-O: being 0.02% or less, and total-N: being 0.02% or less, and with an average aspect ratio of MnS being 10 or less and a maximum aspect ratio of 30 or less.
and the maximum MnS particle size (μm) is 110 × [S%] + 15 or less,
A steel having excellent forgeability and machinability, characterized in that the number of MnS per m2 is 3800 × [S%] + 150 or less, and the balance consisting of Fe and unavoidable impurities.
、最大アスペクト比30以下を有し、残部がFeおよび不可避的不純物よりなる
ことを特徴とする鍛造性と被削性に優れた鋼。[Claim 3] A steel with excellent forgeability and machinability, containing, by mass%, C: 0.1 to 0.85%, Si: 0.01 to 1.5%, Mn: 0.05 to 2.0%, P: 0.003 to 0.2%, S: 0.003 to 0.5%, Zr: 0.0003 to 0.01%, with Al: 0.01% or less, total O: 0.02% or less, and total N: 0.02% or less, and further containing one or more of Cr: 0.01 to 2.0%, Ni: 0.05 to 2.0%, and Mo: 0.05 to 1.0%, and having an average aspect ratio of MnS of 10 or less and a maximum aspect ratio of 30 or less, with the balance being Fe and unavoidable impurities.
、最大アスペクト比30以下を有し、更に、最大MnS粒径(μm)が110×
〔S%〕+15以下、1mm2あたりのMnS数が3800×〔S%〕+150
以下を有し、残部がFeおよび不可避的不純物よりなることを特徴とする鍛造性
と被削性に優れた鋼。[Claim 4] A steel sheet containing, by mass%, C: 0.1 to 0.85%, Si: 0.01 to 1.5%, Mn: 0.05 to 2.0%, P: 0.003 to 0.2%, S: 0.003 to 0.5%, Zr: 0.0003 to 0.01%, with Al: 0.01% or less, total-O: 0.02% or less, total-N: 0.02% or less, and further containing one or more of Cr: 0.01 to 2.0%, Ni: 0.05 to 2.0%, and Mo: 0.05 to 1.0%, and having an average aspect ratio of MnS of 10 or less and a maximum aspect ratio of 30 or less, and further having a maximum MnS particle size (μm) of 110×
[S%] + 15 or less, the number of MnS per 1 mm2 is 3800 × [S%] + 150
A steel having excellent forgeability and machinability, characterized by having the following:
を特徴とする鍛造性と被削性に優れた鋼。[Claim 5] A steel having excellent forgeability and machinability, characterized in that the steel according to any one of claims 1 to 4 contains, in mass %, at least one of V: 0.05 to 1.0%, Nb: 0.005 to 0.2%, and Ti: 0.005 to 0.1%, with the balance consisting of Fe and unavoidable impurities.
とを特徴とする鍛造性と被削性に優れた鋼。[Claim 6] A steel with excellent forgeability and machinability, characterized in that the steel according to any one of claims 1 to 5 contains, in mass %, one or more of the following: Ca: 0.0002 to 0.005%, Mg: 0.0003 to 0.005%, Te: 0.0003 to 0.005%, with the balance consisting of Fe and unavoidable impurities.
を特徴とする鍛造性と被削性に優れた鋼。[Claim 7] A steel having excellent forgeability and machinability, characterized in that the steel according to any one of claims 1 to 6 contains, in mass %, one or two of Bi: 0.05 to 0.5%, Pb: 0.01 to 0.5%, and the balance consisting of Fe and unavoidable impurities.
0005%以上0.004%未満を含み、残部がFeおよび不可避的不純物より
なることを特徴とする鍛造性と被削性に優れた鋼。8. The steel according to any one of claims 1 to 7, wherein the steel contains, in mass %, B: 0.
A steel having excellent forgeability and machinability, characterized in that it contains 0.0005% or more but less than 0.004%, with the balance consisting of Fe and unavoidable impurities.
Applications Claiming Priority (3)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP2000-60199 | 2000-03-06 | ||
| JP2000060199A JP2000319751A (en) | 1999-03-09 | 2000-03-06 | Steel with excellent forgeability and machinability |
| PCT/JP2000/006108 WO2001066814A1 (en) | 2000-03-06 | 2000-09-07 | Steel excellent in suitability for forging and cutting |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| JPWO2001066814A1 true JPWO2001066814A1 (en) | 2003-07-02 |
| JP4267234B2 JP4267234B2 (en) | 2009-05-27 |
Family
ID=18580546
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP2001565415A Expired - Fee Related JP4267234B2 (en) | 2000-03-06 | 2000-09-07 | Hot rolled steel for machine structure with excellent forgeability and machinability |
Country Status (6)
| Country | Link |
|---|---|
| US (1) | US6858101B1 (en) |
| EP (1) | EP1264909B1 (en) |
| JP (1) | JP4267234B2 (en) |
| KR (1) | KR100511652B1 (en) |
| DE (1) | DE60024495T2 (en) |
| WO (1) | WO2001066814A1 (en) |
Families Citing this family (16)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JP3468239B2 (en) * | 2001-10-01 | 2003-11-17 | 住友金属工業株式会社 | Steel for machine structural use and its manufacturing method |
| JP3929029B2 (en) * | 2002-03-12 | 2007-06-13 | 三菱製鋼株式会社 | Sulfur-containing free-cutting steel |
| JP3929035B2 (en) * | 2002-07-03 | 2007-06-13 | 三菱製鋼株式会社 | Sulfur-containing free-cutting machine structural steel |
| WO2004067789A1 (en) * | 2003-01-27 | 2004-08-12 | Nippon Steel Corporation | High strength high toughness high carbon steel wire rod and process for producing the same |
| JP2004332078A (en) * | 2003-05-09 | 2004-11-25 | Sanyo Special Steel Co Ltd | Free-cutting steel for machine structures with excellent chip control |
| RU2262549C1 (en) * | 2004-06-29 | 2005-10-20 | Открытое акционерное общество "Оскольский электрометаллургический комбинат" | Medium-carbon steel with elevated cutting ability |
| JP5194474B2 (en) * | 2006-02-17 | 2013-05-08 | Jfeスチール株式会社 | Steel material and manufacturing method thereof |
| JP4983291B2 (en) * | 2006-02-17 | 2012-07-25 | Jfeスチール株式会社 | Steel |
| JP5147272B2 (en) * | 2007-03-27 | 2013-02-20 | 株式会社神戸製鋼所 | Cold forged non-tempered high-strength steel parts with excellent impact characteristics in the direction perpendicular to the axial direction |
| EP2246451B1 (en) | 2008-02-26 | 2013-10-09 | Nippon Steel & Sumitomo Metal Corporation | Hot forging micro alloyed steel and hot rolled steel material having excellent fracture splittability and machinability, and part thereof. |
| KR101008130B1 (en) | 2008-07-28 | 2011-01-13 | 주식회사 포스코 | Medium carbon sulfur free cutting steel with excellent machinability and molten steel refining method |
| IN2014DN03266A (en) * | 2011-10-20 | 2015-07-10 | Nippon Steel & Sumitomo Metal Corp | |
| JP5873405B2 (en) * | 2012-07-18 | 2016-03-01 | 株式会社神戸製鋼所 | Bearing steel and bearing parts with excellent rolling fatigue characteristics |
| DE102014108311B4 (en) * | 2013-06-13 | 2015-01-15 | Thyssenkrupp Steel Europe Ag | Selection procedure for steel grades |
| US10344363B2 (en) | 2015-10-19 | 2019-07-09 | Nippon Steel & Sumitomo Metal Corporation | Hot-rolled steel and steel component |
| CN109477174A (en) * | 2016-07-04 | 2019-03-15 | 新日铁住金株式会社 | Steel for mechanical structures |
Family Cites Families (10)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JPS4966522A (en) | 1972-10-31 | 1974-06-27 | ||
| US4434006A (en) * | 1979-05-17 | 1984-02-28 | Daido Tokushuko Kabushiki Kaisha | Free cutting steel containing controlled inclusions and the method of making the same |
| JPS5855553A (en) * | 1981-09-29 | 1983-04-01 | Daido Steel Co Ltd | Tool steel |
| JPH0643605B2 (en) * | 1986-03-10 | 1994-06-08 | 住友金属工業株式会社 | Manufacturing method of non-heat treated steel for hot forging |
| JP2638020B2 (en) * | 1987-12-22 | 1997-08-06 | 住友金属工業株式会社 | Free-cutting steel for hot forging |
| JPH0796695B2 (en) * | 1988-08-10 | 1995-10-18 | 新日本製鐵株式会社 | Medium carbon tough steel |
| JPH032351A (en) * | 1989-05-30 | 1991-01-08 | Daido Steel Co Ltd | free cutting steel |
| JP2517790B2 (en) | 1990-09-25 | 1996-07-24 | 株式会社神戸製鋼所 | Wire for welding galvanized steel sheet and welding method |
| JP3503163B2 (en) * | 1993-04-21 | 2004-03-02 | Jfeスチール株式会社 | Machine structural steel with excellent machinability and cold forgeability |
| JPH07188846A (en) * | 1993-12-28 | 1995-07-25 | Kawasaki Steel Corp | Carbon steel for machine structure with excellent machinability and cold forgeability |
-
2000
- 2000-09-07 JP JP2001565415A patent/JP4267234B2/en not_active Expired - Fee Related
- 2000-09-07 DE DE60024495T patent/DE60024495T2/en not_active Expired - Lifetime
- 2000-09-07 EP EP00957014A patent/EP1264909B1/en not_active Expired - Lifetime
- 2000-09-07 US US10/221,119 patent/US6858101B1/en not_active Expired - Lifetime
- 2000-09-07 WO PCT/JP2000/006108 patent/WO2001066814A1/en not_active Ceased
- 2000-09-07 KR KR10-2002-7011650A patent/KR100511652B1/en not_active Expired - Fee Related
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