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JPH0465893B2 - - Google Patents
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JPH0465893B2 - - Google Patents

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Publication number
JPH0465893B2
JPH0465893B2 JP61268915A JP26891586A JPH0465893B2 JP H0465893 B2 JPH0465893 B2 JP H0465893B2 JP 61268915 A JP61268915 A JP 61268915A JP 26891586 A JP26891586 A JP 26891586A JP H0465893 B2 JPH0465893 B2 JP H0465893B2
Authority
JP
Japan
Prior art keywords
less
grain boundary
hardenability
steel
boundary oxidation
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 - Lifetime
Application number
JP61268915A
Other languages
Japanese (ja)
Other versions
JPS63121638A (en
Inventor
Susumu Kanbara
Kenji Aihara
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 JP26891586A priority Critical patent/JPS63121638A/en
Publication of JPS63121638A publication Critical patent/JPS63121638A/en
Publication of JPH0465893B2 publication Critical patent/JPH0465893B2/ja
Granted legal-status Critical Current

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  • Heat Treatment Of Steel (AREA)
  • Solid-Phase Diffusion Into Metallic Material Surfaces (AREA)

Description

【発明の詳細な説明】[Detailed description of the invention]

〔産業上の利用分野〕 本発明は、浸炭焼入れを行つても表面に浸炭異
常組織の生成が殆どなく、機械構造用部品に使用
して高度の疲労強度、転動疲労強度、耐摩耗性を
付与することができる肌焼鋼に関するものであ
る。 〔従来の技術〕 従来、機械構造用部品は、その疲労強度、転動
疲労強度、耐摩耗性を向上せしめるために表面硬
化処理、なかでも特にその効果の大きい浸炭焼入
れが広範に行われている。しかし、従来の肌焼鋼
(例えばJIS−SCr420、SCM420)に浸炭焼入れ
を施すと、浸炭部表面に深さ10〜20μmの結晶粒
界酸化が生じ、これに付随して不完全焼入組織
(トルースタイト)が生成して表面の硬さが低下
してしまう。この浸炭部表面の結晶界酸化と不完
全焼入組織とを合わせて浸炭異常組織と称してい
る。 この異常組織は、浸炭雰囲気中の酸化性ガス
(CO2、H2O)中のOが浸炭中の鋼のオーステナ
イト粒界に優先的に侵入拡散し、Si、Mn、Crの
ようなFeより酸化されやすい元素と結合して酸
化物を形成する上に、この酸化物のために粒界近
傍で固溶Si、固溶Mn、固溶Cr濃度が低下し、こ
れらの相乗として焼入性が極端に低下する結果、
表面で不完全焼入組織が生成されることが原因と
されている。 そして、表層部に粒界酸化物が形成されると、
それが切欠として作用するため、疲労強度、耐衝
撃性が劣化し、さらに粒界酸化物の形成に付随し
て軟かい不完全焼入層が生成することから、疲労
強度、転動疲労強度、耐摩耗性も劣化する。 ところで近年、産業機械、輸送機械、建設機械
などに使われている機械構造用部品に対する耐久
性についての要求はますます高度化してきてお
り、特に繰返し荷重のかかる強度部材では高疲労
強度化、高転動疲労強度化が、また摺動部材では
高耐摩耗性が望まれている。 例えば、自動車のトランスミツシヨンギヤにあ
つては、エンジンの高出力化に伴つて歯元疲労強
度と歯面転動疲労強度の向上が、またプラスチツ
ク成形機、さく岩機などの油圧ピストンおよびシ
リンダーにあつては、機械の大型化、摺動サイク
ルの高速化に伴つて摺動部表面の耐摩耗性の向上
が強く望まれている。 このため従来より、浸炭異常組織の生成を防止
し、疲労強度、耐衝撃性、あるいは耐摩耗性の改
善を目的とした肌焼鋼が、例えば特公昭55−3277
号公報、特開昭60−21359号公報、特開昭60−
243252号公報等により提案されている。 〔発明が解決しようとする問題点〕 しかしながら、これらの提案はいずれも粒界酸
化を助長するSi、Mn、Crの添加量規制のみで対
応しようとするものであり、浸炭条件、焼入条件
によつては、完全に浸炭異常組織を抑えることが
困難である。従つて、近年の機械構造用部品に対
する高度な要求に完全に応えることは難しかつ
た。 また、表層部に圧縮残留応力を導入すれば疲労
強度、転動疲労強度が向上することから、浸炭焼
入れ後にシヨツトピーニングを施すことが従来よ
り行われているが、不完全焼入組織が存在する
と、シヨツトピーニングによる極端な肌荒れ(表
面凸凹)が生じ、かえつて疲労強度が低下するこ
ともあり、効果的な対策とは言えなかつた。 本発明は、このような状況に鑑み、浸炭異常組
織の生成に対して極めて高い抵抗力を示す肌焼鋼
を提供するものである。 〔問題点を解決するための手段〕 本発明者らは、浸炭異常組織の生成を抑制する
ためには、Si、Mn、Crにとらわれることなく広
い成分系から総合的に、しかも粒界酸化と不完全
焼入組織の両面から対策を講じることが必要であ
ると考え、鋭意実験研究を重ねた結果、次の知見
を得るに至つた。 ΓCuを添加すれば粒界酸化が大巾に抑制される
ことが判明した。これは、浸炭中に表層部に
Cuが濃化し、最表面を極めて薄いCu化合物が
覆うため、粒界へのOの侵入を防ぐためと考え
られる。 Γしかし、Cuによる粒界酸化抑制効果は、酸化
物生成自由エネルギーがFeより低い元素、言
い換えればFeより酸化しやすい元素(第1図
に示すように、例えばSi、Mn、Cr、Alなど)
との相互作用が大きく、これらの元素を添加し
過ぎると粒界酸化が抑制できなくなる。 この観点から、極めて酸化しやすいAlは出
来るだけ含まれないのがよく、含まれてもSol.
Alで0.05%未満、次いで酸化しやすいSiについ
ては0.15%未満、Crについては1.5%以下、Mn
については1.2%以下に制限する必要がある。 ΓCuについては、また、Cu化合物被膜の下はCu
濃化層になつており、たとえ粒界酸化により固
溶Si、固溶Mn、固溶Crの量が低下してもCuの
焼入性向上効果で表層部の不完全焼入組織は生
成しにくいことが判明した。 ΓSi、Mn、Crは焼入性を向上させる元素でもあ
るため、これら元素の添加量を前述のように規
制すると、肌焼鋼としての焼入性が確保されな
いばかりでなく、焼入冷媒の種類によつては焼
入時に鋼表面に沸騰膜ができて最表面の冷却速
度が遅くなるため、たとえ内部まで十分に焼入
されたとしても表層部に不完全焼入組織ができ
ることが判明した。 そこで、さらに検討を重ねた結果、Niおよ
びMoは粒界酸化を助長ぜずかつ不完全焼入層
を防止できることが明らかとなつた。これは、
第1図に示すように、NiとMoはFeより酸化物
生成自由エネルギーが高い、すなわちFeより
酸化しにくく、かつ焼入性を向上させる元素で
あるためと考えられる。 母材の焼入性が不足する場合には、Bを添加
するのも有効である。 Γまた、Alの含有量規制によるオーステイト粒
の粗大化に対しては、Nb、Vが有効に働くこ
とも明らかになつた。 本発明は、以上の知見に基づきなされたもの
で、下記の成分組成を基礎とし、これに必要
に応じてまたはもしくは+の成分系を
加えた肌焼鋼を要旨とする。 重量比でC:0.1〜0.4%、Si:0.15%未満、
Mn:1.2%以下、Cr:1.5%以下、Sol.Al:
0.05%未満、Cu:0.02〜0.5%未満を含み、
残部Feおよび不可避的不純物。 重量比でNi:5.0%以下、Mo:2.5%以下、
B:0.005%以下のうち1種または2種以上。 重量比でNb:0.15%以下、V:0.15%以下
の1種または2種 次に本発明鋼の成分範囲限定理由を述べ
る。 ΓC:0.1〜0.4% Cは機械構造用部品としての強度確保のため
に必要な基本成分であり、肌焼鋼として浸炭焼
入、焼戻し後のコア(非浸炭部)の硬さは少な
くともHRC25は必要であり、このためにはC量
は0.1%以上は必要である。 しかし、0.4%を越えて添加すると、ケース
(浸炭部)とコアの硬さの差が小さくなり、疲
労強度向上、転動疲労強度向上に有効な圧縮残
留応力が導入されにくくなるとともに、耐衝撃
性、被削性が劣化するので、上限を0.4%とし
た。 ΓSi:0.15%未満 SiはFeより非常に酸化されやすい元素であ
り、浸炭された表層部で粒界酸化物の生成を著
しく助長する作用を有する。このため少ない方
が好ましいが、0.15%未満では粒界酸化は無視
できる程度に軽微になるため上限を0.15%
(0.15%は含まない)とした。 下限はSiが少ないほど粒界酸化を抑制できる
ので特に規定しないが、製鋼上0.05%より少な
くするには困難をともなうので、好ましくは
0.05%である。 ΓMn:1.2%以下 MnもSiほどではないが、Feより酸化されや
すい元素であり、従つて粒界酸化を助長する。
このため、Mn添加量も少ないほどよいが、Cu
を添加する場合には1.2%以下にすると粒界酸
化物はほとんど生成しなくなる。このためMn
の上限は1.2%とした。 下限はMnが少量ほど粒界酸化を抑制できる
ので特に規定しないが、コア部の焼入性を確保
することを考慮すると0.3%以上が好ましい。 ΓCr:1.5%以下 Crも粒界酸化物を生成しやすい元素であり、
従つてCr添加量も少ないほど好ましい。しか
し、Cuを添加する場合には1.5%以下にすると
粒界酸化物はほとんど生成しなくなる。このた
め、Crの上限は1.5%とした。 下限はCrが少ないほど粒界酸化を抑制でき
るので特に規定しないが、0.5%未満になると
浸炭性が低下するので0.5%以上が好ましい。 ΓSol.Al:0.05%未満 AlはSi、Mn、Crに比べ大巾に酸化しやす
く、粒界酸化を生じる要因になるので、少ない
ほど好ましいが、Cuを添加する場合には、0.05
%未満にすると粒界酸化物はほとんど生成しな
くなる。 下限はAlが少ないほど粒界酸化防止に有効
であるので特に規定しない。 ΓCu:0.02〜0.5%未満 既に述べたようにCuを添加することにより、
最表面に極めて薄いCu化合物層が生じ、粒界
酸化を防止することができる。また、Cu化合
物層の下にはCu濃化層が生じ、たとえ粒界酸
化が生じて表面層の焼入性が低下してもCuの
焼入性向上効果で不完全焼入性組織は生成しに
くくなる。これらの効果を十分に発現されるた
めには少なくとも0.02%のCuが必要であるが、
0.5%を含むより以上の添加は、Cu化合物層の
厚さが厚くなり、浸炭性が急激に低下して不完
全焼入組織の生成が顕著になるので、下限を
0.02%、上限を0.5%未満とした。 ΓNi:5.0%以下 本発明鋼は粒界酸化を防止するために、Fe
より酸化されやすいSi、Mn、Crの添加量を制
限している。これらの元素はいずれも焼入性向
上元素であるため、肌焼鋼としてのコア部の焼
入性が十分に確保されなくなる。また、ケース
においても焼入性が不十分なため、表層部の不
完全焼入組織が生成されやすくなる。従つて、
粒界酸化を生じず、かつ焼入性を高めるNiの
添加は浸炭異常組織(粒界酸化、不完全焼入
層)の防止に有効である。 また、このNiはCu添加による熱間加工性の
劣化を改善する効果も有する。 しかし、Niは5.0%を越えて添加すると浸炭
性が阻害されるとともに、切削性が著しく劣化
するので添加される場合は上限を5.0%とする。 下限についてはCu添加による熱間加工性の
劣化を防止するため、Cu添加量以上にするの
が好ましい。 ΓMo:2.5%以下 MoもNiと同様、粒界酸化を起こさず、焼入
性を向上させる元素であるため、コア部の焼入
性を確保するのみならず、表層部の不完全焼入
組織の防止に役に立つ。しかし、2.5%を越え
て添加すると、浸炭されたケース部において
Mo炭化物が析出し、表層部の焼入性はかえつ
て低下するので添加する場合は上限を2.5%と
する。 下限についてはコア部の焼入性を確保するこ
とを考慮すると、0.1%以上が好ましい。 ΓB:0.005%以下 Bは微量添加で焼入性を著しく向上させる元
素であるが、C量が多くなるほどその効果が薄
れる。従つて、コア部の焼入性だけを向上させ
る場合には非常に有効である。しかし、Bは
Feより酸化しやすい元素でもあり、0.005%を
越えて添加すると表層部に粒界酸化が生成し始
める。このため添加される場合は上限を0.005
%とする。 下限は、焼入性向上効果が顕著になる0.0003
%を越えることが好ましい。 ΓNb:0.01〜0.1%、V:0.01〜0.1% 通常、AlはNと結合して微細なAlNを形成
し、浸炭時のオーステナイト粒の粗大化を阻止
する効果がある。しかし、本発明鋼では粒界酸
化を抑制するために、Alを無添加または添加
量を0.05%未満に制限していることから、浸炭
前の履歴および浸炭条件によつてはオーステナ
イト粒が粗大化する場合がある。これを防止す
るためにはNb、V添加して、NbC、VCを微
細析出させるのが有効である。この効果を十分
に発揮させるためにはNb、Vはいずれも0.01
%以上添加する必要がある。しかし、Nb、V
ともFeより酸化しやすく、0.01%を越えて添加
すると粒界酸化物が生成しはじめる。このため
下限を0.01%、上限を0.1%とした。 〔実施例〕 次に実施例をもつて本発明を説明する。 第1表に示す化学成分を有する42種類の鋼を高
周波真空炉にて溶製し、熱間鍜造により直径40mm
の丸棒と35mm×35mmの角棒にと成形し、角棒から
は第2図に示す曲げ疲労試験片を、丸棒からは第
3図に示す円板状転動疲労試験片をそれぞれ作成
した。 そして、これらの試験片を先ずカーボンポテン
シヤル0.8%の浸炭雰囲気で930℃×2hr保持した
後、200℃のホツトクエンチ油で焼入した。 浸炭焼入後、曲げ疲労試験片の断面を研磨し、
しかる後、無腐食で粒界酸化深さを、ナイタール
腐食により不完全焼入層深さを光学顕微鏡観察に
よつて測定した。測定はそれぞれ20ケ所行い、そ
の平均値をもつて測定値とした。 合せて曲げ疲労試験と転動疲労試験とを行つ
た。曲げ疲労試験は、第4図に示すように、試験
片両端を支持した状態で107回まで中央部に繰返
し圧縮応力を付加して、圧縮応力と繰返し数との
関係をS−N曲線に表わし、その結果から疲労限
度を求めるものとした。 転動疲労試験片については、第5図に示すよう
に、同一試験片どうしの2ローラ式転動疲労試験
(すべり率0%)を107回まで繰返し、押え面圧と
繰返しの数との関係をS−N曲線に表わして、耐
久限度を求めた。 これらの試験結果を第1表に併記する。 鋼種No.1〜No.72は本発明に係る鋼である。一
方、鋼種No.73〜No.75はSi含有量の点で、鋼種No.76
〜No.78はMn含有量の点で、鋼種No.79〜81はCr含
有量の点で、鋼種No.82〜No.85はCu含有量の点で
それぞれ本発明の範囲を外れる比較鋼である。
[Industrial Application Field] The present invention has almost no carburized abnormal structure on the surface even when carburized and quenched, and can be used in mechanical structural parts to achieve high fatigue strength, rolling fatigue strength, and wear resistance. The present invention relates to case hardening steel that can be case hardened. [Prior Art] Conventionally, mechanical structural parts have been widely subjected to surface hardening treatment, particularly carburizing and quenching, which is particularly effective, in order to improve their fatigue strength, rolling contact fatigue strength, and wear resistance. . However, when conventional case hardening steel (e.g. JIS-SCr420, SCM420) is carburized and quenched, grain boundary oxidation with a depth of 10 to 20 μm occurs on the surface of the carburized part, accompanied by an incompletely quenched structure ( troostite) is formed and the surface hardness decreases. The crystal boundary oxidation on the surface of the carburized portion and the incompletely quenched structure are collectively referred to as the abnormal carburized structure. This abnormal structure is caused by O in the oxidizing gases (CO 2 , H 2 O) in the carburizing atmosphere preferentially penetrating and diffusing into the austenite grain boundaries of the steel during carburizing, and is more concentrated than Fe such as Si, Mn, and Cr. In addition to forming oxides by combining with elements that are easily oxidized, these oxides reduce the concentrations of solid solution Si, solid solution Mn, and solid solution Cr near the grain boundaries, and as a result of these factors, hardenability decreases. As a result of the extreme decline,
This is thought to be caused by the formation of an incompletely hardened structure on the surface. Then, when grain boundary oxides are formed in the surface layer,
Since these act as notches, fatigue strength and impact resistance deteriorate, and a soft incompletely quenched layer is generated along with the formation of grain boundary oxides, resulting in fatigue strength, rolling contact fatigue strength, Abrasion resistance also deteriorates. However, in recent years, demands on the durability of mechanical structural parts used in industrial machinery, transportation machinery, construction machinery, etc. have become increasingly sophisticated.In particular, high fatigue strength and high High rolling fatigue strength is desired, and high wear resistance is desired for sliding members. For example, in the case of automobile transmission gears, tooth root fatigue strength and tooth surface rolling fatigue strength have improved as engines become more powerful, and hydraulic pistons and cylinders in plastic molding machines, rock drills, etc. As machines become larger and sliding cycles become faster, there is a strong desire to improve the wear resistance of the surfaces of sliding parts. For this reason, case-hardening steels have been developed for the purpose of preventing the formation of abnormal carburized structures and improving fatigue strength, impact resistance, or wear resistance.
No. 60-21359, JP-A No. 60-21359, JP-A-60-21359
It has been proposed in Publication No. 243252, etc. [Problems to be solved by the invention] However, all of these proposals attempt to solve the problem only by regulating the amount of Si, Mn, and Cr added, which promote grain boundary oxidation. Therefore, it is difficult to completely suppress the carburized abnormal structure. Therefore, it has been difficult to completely meet recent high demands for mechanical structural parts. In addition, introducing compressive residual stress into the surface layer improves fatigue strength and rolling contact fatigue strength, so shot peening has traditionally been performed after carburizing and quenching, but incompletely quenched structures still exist. As a result, the shot peening caused extreme roughness (surface unevenness), which could even reduce fatigue strength, so it could not be said to be an effective countermeasure. In view of this situation, the present invention provides a case hardening steel that exhibits extremely high resistance to the formation of abnormal carburized structures. [Means for Solving the Problems] The present inventors have determined that in order to suppress the formation of abnormal carburized structures, a comprehensive approach should be taken from a wide range of components, not limited to Si, Mn, and Cr, as well as grain boundary oxidation. We believed that it was necessary to take measures from both sides of the incompletely quenched structure, and as a result of extensive experimental research, we came to the following knowledge. It was found that grain boundary oxidation can be greatly suppressed by adding ΓCu. This occurs in the surface layer during carburizing.
This is thought to be because Cu is concentrated and the outermost surface is covered with an extremely thin Cu compound, which prevents O from entering the grain boundaries. Γ However, the effect of suppressing grain boundary oxidation by Cu is limited to elements with lower oxide formation free energy than Fe, in other words, elements that are more easily oxidized than Fe (as shown in Figure 1, for example, Si, Mn, Cr, Al, etc.)
If these elements are added too much, grain boundary oxidation cannot be suppressed. From this point of view, it is best to avoid containing Al, which is extremely easy to oxidize, as much as possible, and even if it is included, it is solvable.
Less than 0.05% for Al, then less than 0.15% for easily oxidized Si, less than 1.5% for Cr, and Mn
It is necessary to limit it to 1.2% or less. Regarding ΓCu, there is also Cu under the Cu compound coating.
Even if the amount of solute Si, solute Mn, and solute Cr decreases due to grain boundary oxidation, an incompletely quenched structure will not form in the surface layer due to the hardenability improvement effect of Cu. It turned out to be difficult. ΓSi, Mn, and Cr are also elements that improve hardenability, so if the amounts of these elements are restricted as described above, not only will the hardenability of case hardening steel not be ensured, but the type of quenching refrigerant will In some cases, a boiling film is formed on the steel surface during quenching, which slows down the cooling rate at the outermost surface, resulting in incompletely quenched structures on the surface layer even if the inside is sufficiently quenched. As a result of further investigation, it became clear that Ni and Mo do not promote grain boundary oxidation and can prevent the formation of incompletely hardened layers. this is,
As shown in FIG. 1, this is thought to be because Ni and Mo have a higher free energy of oxide formation than Fe, that is, they are elements that are more difficult to oxidize than Fe and improve hardenability. When the hardenability of the base material is insufficient, it is also effective to add B. Γ It has also been revealed that Nb and V work effectively against coarsening of austate grains due to regulation of Al content. The present invention has been made based on the above findings, and its gist is a case hardening steel based on the following component composition, with or without additional component systems added thereto as necessary. C: 0.1 to 0.4%, Si: less than 0.15% by weight,
Mn: 1.2% or less, Cr: 1.5% or less, Sol.Al:
Contains less than 0.05%, Cu: 0.02 to less than 0.5%,
Remaining Fe and unavoidable impurities. Weight ratio: Ni: 5.0% or less, Mo: 2.5% or less,
B: One or more of 0.005% or less. One or two types of Nb: 0.15% or less and V: 0.15% or less in weight ratio Next, the reason for limiting the composition range of the steel of the present invention will be described. ΓC: 0.1 to 0.4% C is a basic component necessary to ensure strength as a mechanical structural part, and as a case hardening steel, the hardness of the core (non-carburized part) after carburizing and quenching and tempering is at least H R C25 is necessary, and for this purpose, the amount of C must be 0.1% or more. However, if it is added in excess of 0.4%, the difference in hardness between the case (carburized part) and the core becomes small, making it difficult to introduce compressive residual stress that is effective in improving fatigue strength and rolling contact fatigue strength. The upper limit was set at 0.4% because it deteriorates the hardness and machinability. ΓSi: less than 0.15% Si is an element that is much more easily oxidized than Fe, and has the effect of significantly promoting the formation of grain boundary oxides in the carburized surface layer. For this reason, less is better, but if it is less than 0.15%, grain boundary oxidation will be negligible, so the upper limit should be set at 0.15%.
(0.15% is not included). The lower limit is not particularly stipulated because the lower the Si content, the more grain boundary oxidation can be suppressed, but it is preferable because it is difficult to reduce the Si content to less than 0.05% in terms of steel manufacturing.
It is 0.05%. ΓMn: 1.2% or less Mn is also an element that is more easily oxidized than Fe, although not as much as Si, and therefore promotes grain boundary oxidation.
For this reason, the smaller the amount of Mn added, the better;
When adding 1.2% or less, grain boundary oxides will hardly be generated. For this reason, Mn
The upper limit was set at 1.2%. The lower limit is not particularly defined because the smaller the amount of Mn, the more grain boundary oxidation can be suppressed, but in consideration of ensuring the hardenability of the core part, 0.3% or more is preferable. ΓCr: 1.5% or less Cr is also an element that tends to generate grain boundary oxides,
Therefore, the smaller the amount of Cr added, the more preferable. However, when adding Cu, if the content is 1.5% or less, grain boundary oxides will hardly be generated. For this reason, the upper limit of Cr was set at 1.5%. The lower limit is not particularly specified because the less Cr is, the more grain boundary oxidation can be suppressed, but if it is less than 0.5%, the carburizability will decrease, so 0.5% or more is preferable. ΓSol.Al: Less than 0.05% Al is much more easily oxidized than Si, Mn, and Cr and can cause grain boundary oxidation, so the smaller the better, but when adding Cu, 0.05%
If it is less than %, grain boundary oxides will hardly be generated. The lower limit is not particularly defined because the lower the Al content, the more effective it is in preventing grain boundary oxidation. ΓCu: 0.02 to less than 0.5% As already mentioned, by adding Cu,
An extremely thin Cu compound layer is formed on the outermost surface, which prevents grain boundary oxidation. In addition, a Cu-enriched layer is formed under the Cu compound layer, and even if grain boundary oxidation occurs and the hardenability of the surface layer decreases, an incompletely hardenable structure is formed due to the hardenability-improving effect of Cu. It becomes difficult to do. At least 0.02% Cu is required to fully express these effects, but
Adding more than 0.5% will increase the thickness of the Cu compound layer, sharply reducing carburizability and forming an incompletely quenched structure, so the lower limit should be set.
0.02%, with an upper limit of less than 0.5%. ΓNi: 5.0% or less In order to prevent grain boundary oxidation, the steel of the present invention
The amount of Si, Mn, and Cr, which are more easily oxidized, is limited. Since these elements are all elements that improve hardenability, the hardenability of the core portion as a case hardening steel cannot be sufficiently ensured. Furthermore, since the hardenability of the case is insufficient, incompletely hardened structures are likely to be formed in the surface layer. Therefore,
Addition of Ni, which does not cause grain boundary oxidation and improves hardenability, is effective in preventing abnormal carburized structures (grain boundary oxidation, incompletely hardened layer). Moreover, this Ni also has the effect of improving the deterioration of hot workability caused by the addition of Cu. However, if Ni is added in an amount exceeding 5.0%, carburizing properties are inhibited and machinability is significantly deteriorated, so when Ni is added, the upper limit is set to 5.0%. Regarding the lower limit, in order to prevent deterioration of hot workability due to the addition of Cu, it is preferable to set the amount to be equal to or higher than the amount of Cu added. ΓMo: 2.5% or less Like Ni, Mo is an element that does not cause grain boundary oxidation and improves hardenability, so it not only ensures hardenability in the core but also improves the incompletely hardened structure in the surface layer. It is useful for preventing. However, when added in excess of 2.5%, the carburized case part
Since Mo carbides precipitate and the hardenability of the surface layer deteriorates, the upper limit when adding Mo is 2.5%. The lower limit is preferably 0.1% or more in consideration of ensuring the hardenability of the core portion. ΓB: 0.005% or less B is an element that significantly improves hardenability when added in a small amount, but the effect becomes weaker as the amount of C increases. Therefore, it is very effective in improving only the hardenability of the core portion. However, B
It is also an element that is more easily oxidized than Fe, and when added in excess of 0.005%, grain boundary oxidation begins to occur in the surface layer. Therefore, if added, the upper limit should be 0.005
%. The lower limit is 0.0003, where the hardenability improvement effect becomes noticeable.
It is preferable that it exceeds %. ΓNb: 0.01-0.1%, V: 0.01-0.1% Usually, Al combines with N to form fine AlN, which has the effect of preventing coarsening of austenite grains during carburization. However, in order to suppress grain boundary oxidation in the steel of the present invention, Al is not added or the amount added is limited to less than 0.05%, so depending on the history before carburizing and carburizing conditions, austenite grains may become coarse. There are cases where In order to prevent this, it is effective to add Nb and V to finely precipitate NbC and VC. In order to fully demonstrate this effect, both Nb and V must be 0.01.
It is necessary to add more than %. However, Nb, V
Both are more easily oxidized than Fe, and when added in excess of 0.01%, grain boundary oxides begin to form. Therefore, the lower limit was set to 0.01% and the upper limit was set to 0.1%. [Example] Next, the present invention will be explained with reference to an example. 42 types of steel having the chemical composition shown in Table 1 are melted in a high-frequency vacuum furnace and hot-forged to a diameter of 40 mm.
A round bar and a square bar of 35 mm x 35 mm were formed, and the bending fatigue test piece shown in Figure 2 was made from the square bar, and the disc-shaped rolling fatigue test piece shown in Figure 3 was made from the round bar. did. These test pieces were first held at 930°C for 2 hours in a carburizing atmosphere with a carbon potential of 0.8%, and then quenched with hot quench oil at 200°C. After carburizing and quenching, the cross section of the bending fatigue test piece was polished,
Thereafter, the grain boundary oxidation depth was measured without corrosion, and the depth of the incompletely hardened layer due to nital corrosion was measured by optical microscopic observation. Measurements were performed at 20 locations for each, and the average value was taken as the measured value. In addition, bending fatigue tests and rolling fatigue tests were conducted. In the bending fatigue test, as shown in Figure 4, compressive stress is repeatedly applied to the center of the specimen up to 10 times with both ends supported, and the relationship between the compressive stress and the number of repetitions is plotted as an S-N curve. The fatigue limit was determined from the results. As for the rolling fatigue test pieces, as shown in Figure 5, the two-roller type rolling fatigue test (slip rate 0%) was repeated up to 10 to 7 times on the same test pieces, and the relationship between the presser surface pressure and the number of repetitions was calculated. The relationship was expressed as an S-N curve to determine the durability limit. These test results are also listed in Table 1. Steel types No. 1 to No. 72 are steels according to the present invention. On the other hand, steel grades No. 73 to No. 75 are similar to steel grade No. 76 in terms of Si content.
- No. 78 is a comparative steel that is outside the scope of the present invention in terms of Mn content, steel types No. 79 to 81 in terms of Cr content, and steel types No. 82 to No. 85 in terms of Cu content. It is.

【表】【table】

【表】【table】

【表】【table】

〔発明の効果〕〔Effect of the invention〕

以上の説明から明らかなように、本発明の肌焼
鋼は浸炭異常組織の生成が極端に少ないので、自
動車のトランスミツシヨン、プラスチツク射出成
形機やさく岩機の油圧ピストンおよびシリンダー
など、苛酷な条件で使用される機械構造用部品に
使用して、これに高度の疲労強度、転動疲労強
度、耐摩耗性を与えることができ、これら機械構
造用部品の耐久性向上に大きな効果を発揮するも
のである。
As is clear from the above description, the case-hardened steel of the present invention has extremely little carburized abnormal structure, so it is used in severe applications such as automobile transmissions, plastic injection molding machines, and hydraulic pistons and cylinders of rock drilling machines. It can be used in mechanical structural parts used in various conditions to provide them with high fatigue strength, rolling fatigue strength, and wear resistance, and is highly effective in improving the durability of these mechanical structural parts. It is something.

【図面の簡単な説明】[Brief explanation of the drawing]

第1図は金属酸化物の温度と生成自由エネルギ
ーとの関係を示すグラフ、第2図および第3図は
試験片の形状寸法の説明図、第4図および第5図
は試験方法の説明図、第6図〜第9図は本発明鋼
における特長的元素の浸炭異常組織生成に与える
影響を示したグラフである。
Figure 1 is a graph showing the relationship between temperature and free energy of formation of metal oxides, Figures 2 and 3 are illustrations of the shape and dimensions of the test piece, and Figures 4 and 5 are illustrations of the test method. , and FIGS. 6 to 9 are graphs showing the influence of characteristic elements on the formation of abnormal carburized structures in the steel of the present invention.

Claims (1)

【特許請求の範囲】 1 重量比でC:0.1〜0.4%、Si:0.15%未満、
Mn:1.2%以下、Cr:1.5%以下、Sol.Al:0.05%
未満、Cu:0.02〜0.5%未満を含み、残部Feおよ
び不可避的不純物からなることを特徴とする肌焼
鋼。 2 重量比でC:0.1〜0.4%、Si:0.15%未満、
Mn:1.2%以下、Cr:1.5%以下、Sol.Al:0.05%
未満、Cu:0.02〜0.5%未満を含むとともに、
Ni:5.0%以下、Mo:2.5%以下、B:0.005%以
下のうち1種または2種以上を含有し、残部Fe
および不可避的不純物からなることを特徴とする
肌焼鋼。 3 重量比でC:0.1〜0.4%、Si:0.15%未満、
Mn:1.2%以下、Cr:1.5%以下、Sol.Al:0.05%
未満、Cu:0.02〜0.5%未満を含むとともに、
Nb:0.15%以下、V:0.15%以下の1種または2
種を含有し、残部Feおよび不可避的不純物から
なることを特徴とする肌焼鋼。 4 重量比でC:0.1〜0.4%、Si:0.15%未満、
Mn:1.2%以下、Cr:1.5%以下、Sol.Al:0.05%
未満、Cu:0.02〜0.5%未満を含むとともに、
Ni:5.0%以下、Mo:2.5%以下、B:0.005%以
下のうち1種または2種以上を含有し、さらに
Nb:0.15%以下、V:0.15%以下の1種または2
種を含有し、残部Feおよび不可避的不純物から
なることを特徴とする肌焼鋼。
[Claims] 1. C: 0.1 to 0.4%, Si: less than 0.15% by weight,
Mn: 1.2% or less, Cr: 1.5% or less, Sol.Al: 0.05%
A case hardening steel characterized by containing less than 0.02 to less than 0.5% Cu, with the balance consisting of Fe and inevitable impurities. 2 C: 0.1 to 0.4%, Si: less than 0.15% by weight,
Mn: 1.2% or less, Cr: 1.5% or less, Sol.Al: 0.05%
Cu: less than 0.02 to less than 0.5%, and
Contains one or more of Ni: 5.0% or less, Mo: 2.5% or less, B: 0.005% or less, and the balance is Fe.
Case-hardened steel characterized by comprising: and unavoidable impurities. 3 C: 0.1 to 0.4%, Si: less than 0.15% by weight,
Mn: 1.2% or less, Cr: 1.5% or less, Sol.Al: 0.05%
Cu: less than 0.02 to less than 0.5%, and
Nb: 0.15% or less, V: 0.15% or less type 1 or 2
A case hardening steel characterized by containing seeds and the remainder consisting of Fe and inevitable impurities. 4 C: 0.1 to 0.4%, Si: less than 0.15% by weight,
Mn: 1.2% or less, Cr: 1.5% or less, Sol.Al: 0.05%
Cu: less than 0.02 to less than 0.5%, and
Contains one or more of Ni: 5.0% or less, Mo: 2.5% or less, B: 0.005% or less, and further
Nb: 0.15% or less, V: 0.15% or less type 1 or 2
A case hardening steel characterized by containing seeds and the remainder consisting of Fe and inevitable impurities.
JP26891586A 1986-11-11 1986-11-11 Case hardening steel Granted JPS63121638A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP26891586A JPS63121638A (en) 1986-11-11 1986-11-11 Case hardening steel

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP26891586A JPS63121638A (en) 1986-11-11 1986-11-11 Case hardening steel

Publications (2)

Publication Number Publication Date
JPS63121638A JPS63121638A (en) 1988-05-25
JPH0465893B2 true JPH0465893B2 (en) 1992-10-21

Family

ID=17465040

Family Applications (1)

Application Number Title Priority Date Filing Date
JP26891586A Granted JPS63121638A (en) 1986-11-11 1986-11-11 Case hardening steel

Country Status (1)

Country Link
JP (1) JPS63121638A (en)

Family Cites Families (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS556456A (en) * 1978-06-29 1980-01-17 Daido Steel Co Ltd Blank for surface hardened material having less heat treatment strain
JPS56116857A (en) * 1980-02-20 1981-09-12 Mitsubishi Steel Mfg Co Ltd Low-heat treated strained steel for gear
JPS59182952A (en) * 1983-04-01 1984-10-17 Daido Steel Co Ltd Case hardening steel
JPS6021359A (en) * 1983-07-15 1985-02-02 Daido Steel Co Ltd gear steel

Also Published As

Publication number Publication date
JPS63121638A (en) 1988-05-25

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