JPH07828B2 - Carburized parts - Google Patents

Carburized parts

Info

Publication number
JPH07828B2
JPH07828B2 JP59223899A JP22389984A JPH07828B2 JP H07828 B2 JPH07828 B2 JP H07828B2 JP 59223899 A JP59223899 A JP 59223899A JP 22389984 A JP22389984 A JP 22389984A JP H07828 B2 JPH07828 B2 JP H07828B2
Authority
JP
Japan
Prior art keywords
carbides
less
carburized
major axis
hardened layer
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
JP59223899A
Other languages
Japanese (ja)
Other versions
JPS61104065A (en
Inventor
邦夫 並木
憲二 礒川
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.)
Daido Steel Co Ltd
Original Assignee
Daido Steel Co 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 Daido Steel Co Ltd filed Critical Daido Steel Co Ltd
Priority to JP59223899A priority Critical patent/JPH07828B2/en
Publication of JPS61104065A publication Critical patent/JPS61104065A/en
Publication of JPH07828B2 publication Critical patent/JPH07828B2/en
Anticipated expiration legal-status Critical
Expired - Lifetime legal-status Critical Current

Links

Classifications

    • CCHEMISTRY; METALLURGY
    • C23COATING METALLIC MATERIAL; COATING MATERIAL WITH METALLIC MATERIAL; CHEMICAL SURFACE TREATMENT; DIFFUSION TREATMENT OF METALLIC MATERIAL; COATING BY VACUUM EVAPORATION, BY SPUTTERING, BY ION IMPLANTATION OR BY CHEMICAL VAPOUR DEPOSITION, IN GENERAL; INHIBITING CORROSION OF METALLIC MATERIAL OR INCRUSTATION IN GENERAL
    • C23CCOATING METALLIC MATERIAL; COATING MATERIAL WITH METALLIC MATERIAL; SURFACE TREATMENT OF METALLIC MATERIAL BY DIFFUSION INTO THE SURFACE, BY CHEMICAL CONVERSION OR SUBSTITUTION; COATING BY VACUUM EVAPORATION, BY SPUTTERING, BY ION IMPLANTATION OR BY CHEMICAL VAPOUR DEPOSITION, IN GENERAL
    • C23C8/00Solid state diffusion of only non-metal elements into metallic material surfaces; Chemical surface treatment of metallic material by reaction of the surface with a reactive gas, leaving reaction products of surface material in the coating, e.g. conversion coatings, passivation of metals
    • C23C8/06Solid state diffusion of only non-metal elements into metallic material surfaces; Chemical surface treatment of metallic material by reaction of the surface with a reactive gas, leaving reaction products of surface material in the coating, e.g. conversion coatings, passivation of metals using gases
    • C23C8/08Solid state diffusion of only non-metal elements into metallic material surfaces; Chemical surface treatment of metallic material by reaction of the surface with a reactive gas, leaving reaction products of surface material in the coating, e.g. conversion coatings, passivation of metals using gases only one element being applied
    • C23C8/20Carburising
    • C23C8/22Carburising of ferrous surfaces

Description

【発明の詳細な説明】 (産業上の利用分野) 本発明は、自動車,農業機械,産業機械等を構成する機
械構造用部品に適用され、特に表面の耐摩耗性や疲労強
度が要求される部品として使用される浸炭部品の改良に
関するものである。
DETAILED DESCRIPTION OF THE INVENTION (Industrial field of application) The present invention is applied to parts for machine structures constituting automobiles, agricultural machines, industrial machines, etc., and is particularly required to have surface wear resistance and fatigue strength. The present invention relates to improvement of carburized parts used as parts.

(従来技術) 近年、例えば自動車の軽量化の要請に伴って動力伝達部
品が小型化される傾向にあり、このため各部品に対して
より一層の高強度化が要求されるようになってきてい
る。この場合、動力伝達部品において要求される高強度
化の内容は、疲れ強さと面圧強さの向上に大別される
が、この発明は特に面圧強さの向上に関するものであっ
て、例えば歯車の耐ピッチング性(pitting resistanc
e)の向上を狙いとしたものである。ここで、ピッチン
グと称するのは、上記歯車に作用する辷りを含む高面圧
負荷において、表面を起点とするはく離(pitting)が
生ずる現象を意味するものである。
(Prior Art) In recent years, for example, power transmission parts have tended to be miniaturized in response to a demand for weight reduction of automobiles, and therefore, higher strength is required for each component. There is. In this case, the content of high strength required in the power transmission component is roughly classified into improvement of fatigue strength and surface pressure strength, but the present invention relates particularly to improvement of surface pressure strength. Pitting resistanc
It aims to improve e). Here, the term "pitting" means a phenomenon in which peeling from the surface as a starting point occurs under high surface pressure load including slack acting on the gear.

ところで、従来より面圧強さを向上させるために表面硬
さを上昇させる手段として、浸炭時にカーボンポテンシ
ャルをかなり高めて炭化物をより多く析出させるように
したいわゆる過剰浸炭があり、このような過剰浸炭が行
えるようにした専用鍋が開発されている。しかしなが
ら、この専用鋼ではCr,Moを多量に含有するため高価で
あると同時に、焼入性が過剰となるなどの欠点があり、
そのため用途が限定れるという問題点があった。
By the way, as a means for increasing the surface hardness in order to improve the surface pressure strength, there is so-called excess carburization in which the carbon potential is considerably increased during carburization so that more carbides are precipitated. A special pot designed to be used is being developed. However, this special steel is expensive because it contains a large amount of Cr and Mo, and at the same time has the drawback that the hardenability becomes excessive.
Therefore, there is a problem that the application is limited.

(発明の目的) 本発明は、上述した従来の問題点に着目してなされたも
ので、高面圧下(例えばヘルツ応力200kgf/mm2以上)で
接触,回転する部品において、若干カーボンポテンシャ
ルを高めた程度(例えばC.P.<2%)においても高い硬
さが得られ、特に耐ピッチング性を改善できるようにし
た浸炭部品を提供することを目的としている。
(Object of the invention) The present invention has been made by paying attention to the above-mentioned conventional problems, in which a carbon potential is slightly increased in a part which is contacted and rotated under a high surface pressure (for example, Hertz stress of 200 kgf / mm 2 or more). It is intended to provide a carburized component which can obtain high hardness even at a high level (for example, CP <2%) and can particularly improve pitting resistance.

(発明の構成) 上記した目的に従って、高面圧下で接触、回転する部品
の耐ピッング性を改善するために、ピッチングの発生機
構を詳細に検討した結果、 ピッチングは表層部から発生し、旧オーステナイト
粒界はクラックの発生および伝播経路になりうるもので
あり、特に浸炭時に生じる粒界酸化および粒界に析出し
た炭化物は粒界を弱くすること、 耐ピッチング性向上のためには一定の硬化深さを確
保し、さらに表面硬さを上昇させることが好ましいこ
と、 などが明らかとなり、この発明を完成するに至ったもの
である。
(Structure of the invention) According to the above-mentioned object, in order to improve the pitting resistance of the parts that are contacted and rotated under a high surface pressure, as a result of a detailed examination of the mechanism of pitching generation, it is found that pitching occurs from the surface layer part and the former austenite. Grain boundaries can serve as crack generation and propagation paths.In particular, grain boundary oxidation that occurs during carburization and carbides that precipitate at the grain boundaries weaken the grain boundaries, and a certain hardening depth is required to improve pitting resistance. It has been clarified that it is preferable to secure the hardness and further increase the surface hardness, and the present invention has been completed.

すなわち、本発明による浸炭部品は、重量%で、C:0.10
〜0.30%、Si:0.50%以下、Mn:0.20〜1.50%、Cr:1.6超
〜3.0%、および必要に応じて、Mo:0.05〜0.50%,V:0.0
5〜0.50%,Ti:0.05〜0.50%,Nb:0.05〜0.50%,Ta:0.05
〜0.50%,Zr:0.05〜0.50%のうちの1種または2種以上
を含み、残部実質的にFeよりなる鋼を素材とし、Hv550
以上の有効硬化層深さが0.4mm以上、表面硬さがHv800以
上であって、さらに表面から0.1mm以内の範囲に形成さ
れる炭化物の面積率が10〜40%、長径が5μm以下でか
つ80%以上の炭化物の長径/短径の比が2以下であるこ
とを特徴としている。
That is, the carburized part according to the invention has a C: 0.10% by weight.
~ 0.30%, Si: 0.50% or less, Mn: 0.20 to 1.50%, Cr: over 1.6 to 3.0%, and if necessary, Mo: 0.05 to 0.50%, V: 0.0
5 to 0.50%, Ti: 0.05 to 0.50%, Nb: 0.05 to 0.50%, Ta: 0.05
~ 0.50%, Zr: 0.05 ~ 0.50%, one or more of them, and the balance is made of steel consisting essentially of Fe. Hv550
The effective hardened layer depth is 0.4 mm or more, the surface hardness is Hv800 or more, the area ratio of carbides formed within 0.1 mm from the surface is 10 to 40%, and the major axis is 5 μm or less, and It is characterized in that the ratio of major axis / minor axis of carbides of 80% or more is 2 or less.

次に、本発明による浸炭部品を構成する素材の成分範囲
(重量%)の限定理由について説明する。
Next, the reason for limiting the component range (% by weight) of the material constituting the carburized component according to the present invention will be described.

C:0.10〜0.30% Cは浸炭部品の心部強さを確保するのに必要な元素であ
り、このためには0.10%以上添加する。しかし、多すぎ
ると靱性が劣化するので0.30%以下とした。
C: 0.10 to 0.30% C is an element necessary to secure the core strength of carburized parts, and for this purpose, 0.10% or more is added. However, if it is too large, the toughness deteriorates, so the content was made 0.30% or less.

Si:0.50%以下 Siは浸炭時の粒界酸化を助長する元素であり、耐ピッチ
ング性を劣化させるので、0.50%以下とした。そして、
特に通常のガス浸炭を行う場合はSi量は低い程良く、よ
り好ましくは0.15%以下、さらに好ましくは0.10%以下
とするのが良い。
Si: 0.50% or less Si is an element that promotes grain boundary oxidation during carburization and deteriorates pitting resistance, so it is set to 0.50% or less. And
In particular, when performing normal gas carburization, the lower the Si content, the better. More preferably, it is 0.15% or less, further preferably 0.10% or less.

Mn:0.20〜1.50% Mnは溶製時の脱酸剤として添加する元素であり、このた
めには0.20%以上添加する。しかし、多すぎると他元素
とのバランスにもよるが焼入性が過大となり、焼入歪の
原因ともなるので、1.50%以下にした。
Mn: 0.20 to 1.50% Mn is an element added as a deoxidizing agent during melting, and for this purpose, 0.20% or more is added. However, if the amount is too large, the hardenability becomes excessive, depending on the balance with other elements, and it may cause quenching strain, so it was set to 1.50% or less.

Cr:1.6超〜3.0% Crは浸炭時に炭化物(セメンタイト)を析出し、表面層
の硬さを上昇させて浸炭部品の耐ピッチング性を向上さ
せる元素である。そして、このような効果を得るために
は1.6%超添加する必要がある。しかし、添加量が多す
ぎると焼入性が過大となるので3.0%以下に限定した。
Cr: over 1.6% to 3.0% Cr is an element that precipitates carbides (cementite) during carburization and increases the hardness of the surface layer to improve the pitting resistance of carburized parts. And, in order to obtain such an effect, it is necessary to add more than 1.6%. However, if the addition amount is too large, the hardenability becomes excessive, so the content was limited to 3.0% or less.

Mo:0.05〜0.50%,V:0.05〜0.50%,Ti:0.05〜0.50%,Nb:
0.05〜0.50%,Ta:0.05〜0.50%,Zr:0.05〜0.50%のうち
の1種または2種以上 Mo,V,Ti,Nb,Ta,Zrはいずれも炭化物形成元素であって、
それぞれセメンタイトに比べてさらに硬質の炭化物を形
成して表面層の硬さの上昇に寄与し、耐ピッチング性を
より一層向上させるのに有効な元素であるので、必要に
応じてこれらの元素の1種または2種以上を各々0.05%
以上添加するのもよい。しかし、過剰に添加すると炭化
物が粗大となってむしろ耐ピッチング性を低下させるの
で、各々0.50%以下とする必要がある。
Mo: 0.05 to 0.50%, V: 0.05 to 0.50%, Ti: 0.05 to 0.50%, Nb:
One or more of 0.05 to 0.50%, Ta: 0.05 to 0.50%, Zr: 0.05 to 0.50% Mo, V, Ti, Nb, Ta, Zr are all carbide forming elements,
Each of them is an element effective in forming carbides that are harder than cementite and contributing to an increase in the hardness of the surface layer and further improving the pitting resistance. 0.05% for each species or two or more species
It is also possible to add the above. However, if added excessively, the carbides will become coarse and rather the pitting resistance will be reduced, so it is necessary to make each 0.50% or less.

本発明による浸炭部品は、上記の組成になる鋼を素材と
し、Hv550以上の有効硬化層深さが0.4mm以上、表面硬さ
がHv800以上であって、さらに表面から0.1mm以内の範囲
に形成される炭化物の面積率が10〜40%、長径が5μm
以下でかつ80%以上の炭化物の長径/短径の比すなわち
アスペクト比が2以下であることを特徴とするものであ
るが、このように限定した理由について以下に詳述す
る。
The carburized component according to the present invention is made of steel having the above composition as a raw material, has an effective hardened layer depth of Hv550 or more of 0.4 mm or more, a surface hardness of Hv800 or more, and is formed within a range of 0.1 mm or less from the surface. Area ratio of carbides to be used is 10-40%, major axis is 5 μm
It is characterized in that the ratio of the major axis / minor axis of the carbide is 80% or more, that is, the aspect ratio is 2 or less, and the reason for such limitation is described in detail below.

まず、有効硬化層深さおよび表面硬さについては、ピッ
チング試験機を用い、耐ピッチング性に及ぼす硬化特性
の影響を調べたところ、有効硬化層深さについては第1
図に示すような結果が得られ、表面硬さについては第2
図に示すような結果が得られた。
First, regarding the effective hardened layer depth and the surface hardness, when the effect of the hardening characteristics on the pitting resistance was examined using a pitching tester, the effective hardened layer depth was
The results shown in the figure are obtained, and the surface hardness is
The results shown in the figure were obtained.

第1図に示すように、Hv550以上の有効硬化層深さが0.4
mm以上であると耐ピッチング性が著しく向上し、第2図
に示すように、表面硬さがHV800以上であると上記と同
様に耐ピッチング性が著しく向上することが確かめられ
た。
As shown in Fig. 1, the effective hardened layer depth above Hv550 is 0.4.
It was confirmed that when the thickness was not less than mm, the pitting resistance was remarkably improved, and as shown in FIG. 2, when the surface hardness was HV800 or more, the pitting resistance was remarkably improved similarly to the above.

次に、炭化物については、表面から0.1mm以内の範囲に
形成される炭化物の面積率が10%よりも少ないと上記の
表面硬さHv800以上を得ることができず、40%を超える
と粗大炭化物が生じやすくなり、長径が5μmよりも大
きくかつ80%以上の炭化物の長径/短径の比すなわちア
スペクト比が2よりも大きい棒状炭化物および粒界に析
出した網状炭化物が生成されるとそれがピッチングの起
点となりうるので好ましくないためである。
Next, regarding carbides, if the area ratio of carbides formed within the range of 0.1 mm from the surface is less than 10%, the above surface hardness Hv 800 or more cannot be obtained, and if it exceeds 40%, coarse carbides When a rod-shaped carbide having a major axis length of more than 5 μm and a major axis / minor axis ratio of carbide of 80% or more, that is, an aspect ratio of more than 2, and a reticulated carbide precipitated at a grain boundary are formed, pitching occurs. It is not preferable because it can be the starting point.

(実施例) 第1表に示す化学成分の鋼を溶製したのち各鋼よりピッ
チング試験片を作製した。次いで、各ピッチング試験片
に対して第2表に示す条件で表面硬化処理を行った。な
お、表面硬化処理において、浸炭時には温度および浸炭
期−拡散期時間のバランスを考慮して第2表に示す炭素
ポテンシャルを設定した。また、一部については浸炭処
理のほかに、複合熱処理として高周波焼入れおよびレー
ザー焼入れを施した。この場合、浸炭処理後、表面温度
が900〜950℃となるように短時間加熱した後冷却した。
(Example) Pitching test pieces were prepared from each steel after the steel having the chemical composition shown in Table 1 was melted. Then, each of the pitching test pieces was subjected to a surface hardening treatment under the conditions shown in Table 2. In the surface hardening treatment, the carbon potential shown in Table 2 was set in consideration of the temperature and the balance between the carburizing period and the diffusion period during carburization. In addition, in addition to carburizing, a part of them was subjected to induction hardening and laser hardening as a composite heat treatment. In this case, after the carburizing treatment, heating was performed for a short time so that the surface temperature was 900 to 950 ° C., and then cooling was performed.

次いで、各試験片における浸炭層の性状を調べたとこ
ろ、同じく第2表に示す結果が得られた。
Then, when the properties of the carburized layer in each test piece were examined, the same results as shown in Table 2 were obtained.

第2表に示すように、本発明A,Bの試験片における浸炭
層はいずれも上述した各条件を満足するものであり、浸
炭処理のほかにさらに高周波焼入れを施したB′では表
面硬さがさらに高く、有効硬化層深さが大となっている
と共に炭化物も微細化していた。
As shown in Table 2, the carburized layers of the test pieces of the present invention A and B all satisfy the above-mentioned conditions, and the surface hardness of the carburized B ′ is further hardened by induction hardening. Was higher, the effective hardened layer depth was larger, and the carbides were also finer.

また、炭化物形成元素を添加したD,E,F,Gでは炭化物量
が増大しており、複合熱処理を施したD′,F′では表面
硬さがさらに高く、有効硬化層深さが大となっていると
共に炭化物も微細化していた。
Further, the amount of carbides increased in D, E, F, and G to which the carbide-forming element was added, and the surface hardness was higher and the effective hardened layer depth was larger in D'and F'which were subjected to the composite heat treatment. And the carbides were also becoming finer.

一方、比較のH(SCM 420)では表面硬さが低く、炭化
物の面積率も少ないものであった。また、浸炭時の炭素
ポテンシャルが0.80と低い場合(A′)は表面硬さが低
く、表面硬化層深さが小さく、炭化物面積率も少ないも
のであり、反対に浸炭時の炭素ポテンシャルが2.30と高
い場合(E′)には有効硬化層深さはかなり大きくなる
ものの、棒上炭化物が多く生じ、アスペクト比2以下の
炭化物の割合が低いものとなっていた。このことから浸
炭時の炭素ポテンシャルは1.0〜2.0程度とするのが好ま
しいことがわかった。
On the other hand, Comparative H (SCM 420) had a low surface hardness and a small area ratio of carbides. When the carbon potential during carburization is as low as 0.80 (A '), the surface hardness is low, the surface hardened layer depth is small, and the area ratio of carbides is small. On the contrary, the carbon potential during carburization is 2.30. When it was high (E '), the effective hardened layer depth was considerably large, but a large amount of carbides on the rod was generated, and the proportion of carbides having an aspect ratio of 2 or less was low. From this, it was found that the carbon potential during carburization is preferably about 1.0 to 2.0.

次に、上記の熱処理を施した後の各ピッチング試験片に
対して、第3図に示すように、直径d1=130mm,幅W1=18
mmの大ローラ1と、直径d2=26mm,長さl1=130mmのボス
付小ローラ(試験片)2とを高面圧下で接触回転させる
ピッチング試験を行い、小ローラ(試験片)2に大きさ
0.5mmのピッチングが生じた時点を寿命とした。この結
果を第3表に示す。なお、ピッチング試験における面圧
は300および350kgf/mm2,すべり率は40%、油温は40〜5
0℃,回転数は1000r.p.mとした。
Next, as shown in FIG. 3, for each pitching test piece after the above heat treatment, the diameter d 1 = 130 mm and the width W 1 = 18.
A large roller 1 of mm and a small roller (test piece) 2 with a boss having a diameter d 2 = 26 mm and a length l 1 = 130 mm are brought into contact rotation under high surface pressure to perform a pitching test, and a small roller (test piece) 2 To size
The life was defined when 0.5 mm pitching occurred. The results are shown in Table 3. The surface pressure in the pitching test was 300 and 350 kgf / mm 2 , the slip ratio was 40%, and the oil temperature was 40-5.
The temperature was 0 ° C and the rotation speed was 1000 rpm.

第3表に示すように、本発明(1)(2)ではいずれも
比較のものよりもピッチング発生までの寿命が延長して
いることが明らかであり、炭化物生成元素を添加した鋼
を素材としたものの方がよりピッチングが発生しにくく
なっていることが明らかである。また、複合熱処理を施
したB′,D′,F′では、高周波焼入れやレーザー焼入れ
等の際焼入れによって新たなオーステイナイト粒界が形
成されるため、粒界に沿ったクラックは発生しにくく、
ピッチング寿命も良好であることが認められた。これに
対して従来のSCM420を素材としたもの(H)および浸炭
時の炭素ポテンシャルが低いもの(A′)では表面硬さ
が低くまた有効硬化層深さも小さいためピッチング発生
までの寿命が短く、また浸炭時の炭素ポテンシャルが高
いもの(E′)では表面硬さが高く有効硬化層深さも十
分であるが、炭化物が粗大であってかつ粒界に析出して
いるため、これに沿ってクラックが発生しやすくピッチ
ング発生までの寿命が短いものであった。
As shown in Table 3, it is clear that in the present inventions (1) and (2), the life until pitting occurs is longer than that of the comparative examples, and the steel containing the carbide-forming element is used as the raw material. It is obvious that pitching is less likely to occur in the case of the above. Further, in the case of B ', D', and F'which has been subjected to the composite heat treatment, a new austenite grain boundary is formed by quenching during induction hardening or laser hardening, so cracks along the grain boundary are less likely to occur. ,
It was confirmed that the pitting life was also good. On the other hand, the conventional SCM420 material (H) and the low carbon potential during carburization (A ') have a low surface hardness and a small effective hardened layer depth, resulting in a short life until pitting occurs. In the case of carburizing with a high carbon potential (E '), the surface hardness is high and the effective hardened layer depth is sufficient, but since the carbide is coarse and precipitates at the grain boundaries, cracks follow this. Was easily generated, and the life before pitching was short.

なお、本発明において適用されす浸炭処理は、通常のガ
ス浸炭のみならず、真空浸炭や浸炭窒化処理等がある。
そして、この場合にも炭素ポテンシャルは、1.0〜2.0の
範囲として炭化物を形成させるようにすることが好まし
い。
The carburizing treatment applied in the present invention includes not only ordinary gas carburizing but also vacuum carburizing and carbonitriding.
Also in this case, it is preferable that the carbon potential is in the range of 1.0 to 2.0 so that carbides are formed.

また、複合熱処理を行なう場合には、上記の高周波焼入
れやレーザー焼入れに限らず、その他の短時間焼入れで
も同等な効果が得られ、例えばエレクトロンビーム加
熱、プラズマ加熱なども採用しうるものである。
Further, when performing the composite heat treatment, the same effect can be obtained not only by the induction hardening or the laser hardening described above but also by other hardening for a short time. For example, electron beam heating or plasma heating can be adopted.

さらに、鋼の溶製にあたっては、溶製時にエレクトロス
ラグ再溶解(ESR)や真空アーク溶解(VAR)あるいはこ
れらの組合わせ等によって再溶解を行い、初期炭化物
(未溶解炭化物)の微細化をはかるようにすることも望
ましい。また、前述したように、浸炭時の粒界酸化を助
長して耐ピッチング性を劣化させるSi量を極力少なくす
ることも望ましい。
In addition, when smelting steel, remelting is performed by electroslag remelting (ESR), vacuum arc melting (VAR), or a combination of these at the time of smelting to reduce the size of initial carbides (unmelted carbides). It is also desirable to do so. Further, as described above, it is also desirable to minimize the amount of Si that promotes grain boundary oxidation during carburization and deteriorates pitting resistance.

(発明の効果) 以上説明してきたように、本発明による浸炭部品は、重
量%で、C:0.10〜0.30%、Si:0.50%以下、Mn:0.20〜1.
50%、Cr:1.6超〜3.0%、および必要に応じて、Mo:0.05
〜0.50%,V:0.05〜0.50%,Ti:0.05〜0.50%,Nb:0.05〜
0.50%,Ta:0.05〜0.50%,Zr:0.05〜0.50%のうちの1種
または2種以上を含み、残部実質的にFeよりなる鋼を素
材とし、Hv550以上の有効硬化層深さが0.4mm以上、表面
硬さがHv800以上であって、さらに表面から0.1mm以内の
範囲に形成される炭化物の面積率が10〜40%、長径が5
μm以下でかつ80%以上の炭化物の長径/短径の比が2
以下となっているものであるから、炭素ポテンシャルを
若干上げた程度の通常の浸炭処理においても高い硬さが
得られ、耐ピッチング性の高い部品を提供することが可
能であり、例えば自動車の動力伝達部品として使用され
る歯車等の構造部品の小型化および高強度化の要求に対
処しうるものであるという非常に優れた効果がもたらさ
れる。
(Effects of the Invention) As described above, the carburized component according to the present invention is, by weight%, C: 0.10 to 0.30%, Si: 0.50% or less, and Mn: 0.20 to 1.
50%, Cr: over 1.6 to 3.0%, and, if necessary, Mo: 0.05
~ 0.50%, V: 0.05 ~ 0.50%, Ti: 0.05 ~ 0.50%, Nb: 0.05 ~
0.50%, Ta: 0.05 to 0.50%, Zr: 0.05 to 0.50%, containing 1 or 2 or more types, the balance is made of steel consisting essentially of Fe, and the effective hardened layer depth of Hv550 or more is 0.4. mm or more, surface hardness is Hv800 or more, and the area ratio of carbides formed within 0.1 mm from the surface is 10 to 40% and the major axis is 5
The ratio of major axis / minor axis of carbides with a diameter of less than μm and 80% or more is 2
Since it is as follows, it is possible to obtain a high hardness even in the ordinary carburizing treatment with a slightly increased carbon potential, and it is possible to provide a component with high pitting resistance. This is a very excellent effect that can meet the demands for downsizing and high strength of structural parts such as gears used as transmission parts.

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

第1図は浸炭素部品の有効硬化層深さによる耐ピッチン
グ性に及ぼす影響を調べた結果の一例を示すグラフ、第
2図は浸炭部品の表面硬さによる耐ピッチング性に及ぼ
す影響を調べた結果の一例を示すグラフ、第3図はピッ
チング試験の要領を示す説明図である。
Fig. 1 is a graph showing an example of the result of examining the effect of the effective hardened layer depth of the carburized part on the pitting resistance, and Fig. 2 is the effect of the surface hardness of the carburized part on the pitting resistance. FIG. 3 is a graph showing an example of the results, and FIG. 3 is an explanatory view showing the procedure of the pitching test.

Claims (2)

【特許請求の範囲】[Claims] 【請求項1】重量%で、C:0.10〜0.30%、Si:0.50%以
下、Mn:0.20〜1.50%、Cr:1.6超〜3.0%を含み、残部実
質的にFeよりなる鋼を素材とし、Hv550以上の有効硬化
層深さが0.4mm以上、表面硬さがHv800以上であって、さ
らに表面から0.1mm以内の範囲に形成される炭化物の面
積率が10〜40%、長径が5μm以下でかつ80%以上の炭
化物の長径/短径の比が2以下であることを特徴とする
浸炭部品。
1. A steel material containing C: 0.10 to 0.30%, Si: 0.50% or less, Mn: 0.20 to 1.50%, Cr: more than 1.6 to 3.0%, and the balance substantially consisting of Fe, as a raw material. , Hv550 or more effective hardened layer depth is 0.4 mm or more, surface hardness is Hv800 or more, and the area ratio of carbides formed within the range of 0.1 mm from the surface is 10 to 40%, and the major axis is 5 μm or less. And a ratio of major axis / minor axis of carbides of 80% or more to 2 or less, a carburized part.
【請求項2】重量%で、C:0.10〜0.30%、Si:0.50%以
下、Mn:0.20〜1.50%、Cr:1.6超〜3.0%、およびMo:0.0
5〜0.50%,V:0.05〜0.50%,Ti:0.05〜0.50%,Nb:0.05〜
0.50%,Ta:0.05〜0.50%,Zr:0.05〜0.50%のうちの1種
または2種以上を含み、残部実質的にFeよりなる鋼を素
材とし、Hv550以上の有効硬化層深さが0.4mm以上、表面
硬さがHv800以上であって、さらに表面から0.1mm以内の
範囲に形成される炭化物の面積率が10〜40%、長径が5
μm以下でかつ80%以上の炭化物の長径/短径の比が2
以下であることを特徴とする浸炭部品。
2. In weight%, C: 0.10 to 0.30%, Si: 0.50% or less, Mn: 0.20 to 1.50%, Cr: more than 1.6 to 3.0%, and Mo: 0.0.
5 to 0.50%, V: 0.05 to 0.50%, Ti: 0.05 to 0.50%, Nb: 0.05 to
0.50%, Ta: 0.05 to 0.50%, Zr: 0.05 to 0.50%, containing 1 or 2 or more types, the balance is made of steel consisting essentially of Fe, and the effective hardened layer depth of Hv550 or more is 0.4. mm or more, surface hardness is Hv800 or more, and the area ratio of carbides formed within 0.1 mm from the surface is 10 to 40% and the major axis is 5
The ratio of major axis / minor axis of carbides with a diameter of less than μm and 80% or more is 2
Carburized parts characterized by the following.
JP59223899A 1984-10-26 1984-10-26 Carburized parts Expired - Lifetime JPH07828B2 (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP59223899A JPH07828B2 (en) 1984-10-26 1984-10-26 Carburized parts

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP59223899A JPH07828B2 (en) 1984-10-26 1984-10-26 Carburized parts

Publications (2)

Publication Number Publication Date
JPS61104065A JPS61104065A (en) 1986-05-22
JPH07828B2 true JPH07828B2 (en) 1995-01-11

Family

ID=16805447

Family Applications (1)

Application Number Title Priority Date Filing Date
JP59223899A Expired - Lifetime JPH07828B2 (en) 1984-10-26 1984-10-26 Carburized parts

Country Status (1)

Country Link
JP (1) JPH07828B2 (en)

Families Citing this family (5)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
EP0393137B1 (en) * 1987-12-21 1996-09-11 Caterpillar Inc. Carburized low silicon steel article and process
GB8828130D0 (en) * 1988-12-02 1989-01-05 British Petroleum Co Plc Method of identifying dna sequences in chromosomes of plants
JPH0759733B2 (en) * 1989-02-10 1995-06-28 新日本製鐵株式会社 Steel for carburizing
JP3308377B2 (en) * 1994-03-09 2002-07-29 大同特殊鋼株式会社 Gear with excellent tooth surface strength and method of manufacturing the same
US7169238B2 (en) * 2003-12-22 2007-01-30 Caterpillar Inc Carbide method and article for hard finishing resulting in improved wear resistance

Citations (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS5569252A (en) * 1978-11-20 1980-05-24 Komatsu Ltd Carburizing method for steel
JPS5743960A (en) * 1980-08-29 1982-03-12 Mitsubishi Steel Mfg Co Ltd Drill stem with excellent heat resistance, corrosion resistance and abrasion resistance

Patent Citations (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS5569252A (en) * 1978-11-20 1980-05-24 Komatsu Ltd Carburizing method for steel
JPS5743960A (en) * 1980-08-29 1982-03-12 Mitsubishi Steel Mfg Co Ltd Drill stem with excellent heat resistance, corrosion resistance and abrasion resistance

Also Published As

Publication number Publication date
JPS61104065A (en) 1986-05-22

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