JP2541160B2 - Rolling bearing - Google Patents

Rolling bearing

Info

Publication number
JP2541160B2
JP2541160B2 JP3178191A JP17819191A JP2541160B2 JP 2541160 B2 JP2541160 B2 JP 2541160B2 JP 3178191 A JP3178191 A JP 3178191A JP 17819191 A JP17819191 A JP 17819191A JP 2541160 B2 JP2541160 B2 JP 2541160B2
Authority
JP
Japan
Prior art keywords
amount
carbides
rolling
vol
carbide
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
JP3178191A
Other languages
Japanese (ja)
Other versions
JPH0525609A (en
Inventor
恭三郎 古村
保夫 村上
宣晶 三田村
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.)
NSK Ltd
Original Assignee
NSK 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 NSK Ltd filed Critical NSK Ltd
Priority to JP3178191A priority Critical patent/JP2541160B2/en
Priority to GB9215243A priority patent/GB2258274B/en
Publication of JPH0525609A publication Critical patent/JPH0525609A/en
Priority to US08/134,588 priority patent/US5427457A/en
Application granted granted Critical
Publication of JP2541160B2 publication Critical patent/JP2541160B2/en
Anticipated expiration legal-status Critical
Expired - Lifetime legal-status Critical Current

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Classifications

    • FMECHANICAL ENGINEERING; LIGHTING; HEATING; WEAPONS; BLASTING
    • F16ENGINEERING ELEMENTS AND UNITS; GENERAL MEASURES FOR PRODUCING AND MAINTAINING EFFECTIVE FUNCTIONING OF MACHINES OR INSTALLATIONS; THERMAL INSULATION IN GENERAL
    • F16CSHAFTS; FLEXIBLE SHAFTS; ELEMENTS OR CRANKSHAFT MECHANISMS; ROTARY BODIES OTHER THAN GEARING ELEMENTS; BEARINGS
    • F16C33/00Parts of bearings; Special methods for making bearings or parts thereof
    • F16C33/30Parts of ball or roller bearings
    • F16C33/58Raceways; Race rings
    • F16C33/62Selection of substances
    • CCHEMISTRY; METALLURGY
    • C21METALLURGY OF IRON
    • C21DMODIFYING THE PHYSICAL STRUCTURE OF FERROUS METALS; GENERAL DEVICES FOR HEAT TREATMENT OF FERROUS OR NON-FERROUS METALS OR ALLOYS; MAKING METAL MALLEABLE, e.g. BY DECARBURISATION OR TEMPERING
    • C21D9/00Heat treatment, e.g. annealing, hardening, quenching or tempering, adapted for particular articles; Furnaces therefor
    • C21D9/36Heat treatment, e.g. annealing, hardening, quenching or tempering, adapted for particular articles; Furnaces therefor for balls; for rollers
    • 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
    • C23C8/28Solid 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 more than one element being applied in one step
    • C23C8/30Carbo-nitriding
    • C23C8/32Carbo-nitriding of ferrous surfaces
    • FMECHANICAL ENGINEERING; LIGHTING; HEATING; WEAPONS; BLASTING
    • F16ENGINEERING ELEMENTS AND UNITS; GENERAL MEASURES FOR PRODUCING AND MAINTAINING EFFECTIVE FUNCTIONING OF MACHINES OR INSTALLATIONS; THERMAL INSULATION IN GENERAL
    • F16CSHAFTS; FLEXIBLE SHAFTS; ELEMENTS OR CRANKSHAFT MECHANISMS; ROTARY BODIES OTHER THAN GEARING ELEMENTS; BEARINGS
    • F16C33/00Parts of bearings; Special methods for making bearings or parts thereof
    • F16C33/30Parts of ball or roller bearings
    • CCHEMISTRY; METALLURGY
    • C21METALLURGY OF IRON
    • C21DMODIFYING THE PHYSICAL STRUCTURE OF FERROUS METALS; GENERAL DEVICES FOR HEAT TREATMENT OF FERROUS OR NON-FERROUS METALS OR ALLOYS; MAKING METAL MALLEABLE, e.g. BY DECARBURISATION OR TEMPERING
    • C21D1/00General methods or devices for heat treatment, e.g. annealing, hardening, quenching or tempering
    • C21D1/78Combined heat-treatments not provided for above

Landscapes

  • Engineering & Computer Science (AREA)
  • Chemical & Material Sciences (AREA)
  • General Engineering & Computer Science (AREA)
  • Mechanical Engineering (AREA)
  • Metallurgy (AREA)
  • Materials Engineering (AREA)
  • Organic Chemistry (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Physics & Mathematics (AREA)
  • Thermal Sciences (AREA)
  • Crystallography & Structural Chemistry (AREA)
  • Rolling Contact Bearings (AREA)
  • Solid-Phase Diffusion Into Metallic Material Surfaces (AREA)

Description

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

【0001】[0001]

【産業上の利用分野】本発明は転がり軸受に係り、特
に、自動車,農業機械,建設機械及び鉄鋼機械等のトラ
ンスミッション,エンジン用等に使用する転がり軸受の
寿命向上に関する。
BACKGROUND OF THE INVENTION 1. Field of the Invention The present invention relates to a rolling bearing, and more particularly to improving the life of rolling bearings used for transmissions, engines, etc. of automobiles, agricultural machines, construction machines and steel machines.

【0002】[0002]

【従来の技術】軸受潤滑油中に混入している金属の切
粉,削り屑,バリ及び摩耗粉等の異物が転がり軸受の軌
道輪や転動体に損傷を与え、転がり軸受の寿命の大幅な
低下をもたらすことはよく知られている。そこで、本出
願人は先に出願した特開昭64−55423号により、
異物が混入している潤滑下で転がり軸受を使用する場合
でも、軸受の転がり表面層のCの含有量、残留オーステ
ナイト量、及び炭窒化物の含有量を適性値にすること
で、異物により生じる圧痕のエッジ部における応力の集
中を緩和し、クラックの発生を抑え、転がり軸受の寿命
を向上することを提案した。これによれば、適当量の残
留オーステナイトにより異物混入潤滑下での寿命向上を
図ることができるのであるが、一方で、残留オーステナ
イトにより表面硬さが低下して耐疲労性が下がるという
問題があった。また、軸受寿命を向上する上での炭化
物,炭窒化物の粒径の影響にについて、特に、大型炭化
物が繰り返し応力を受けると、その大型炭化物が疲労起
点となりクラック,フレーキングが発生するという点が
考慮されていなかった。
2. Description of the Related Art Foreign matter such as metal chips, shavings, burrs and abrasion powder mixed in bearing lubricating oil damages the races and rolling elements of rolling bearings, resulting in a long life of rolling bearings. It is well known to bring about a decline. Therefore, the applicant of the present invention filed Japanese Patent Application Laid-Open No. 64-55423,
Even when a rolling bearing is used under lubrication containing foreign matter, it is caused by foreign matter by adjusting the content of C in the rolling surface layer of the bearing, the amount of retained austenite, and the content of carbonitride to appropriate values. We proposed to reduce the concentration of stress at the edge of the indentation, suppress the occurrence of cracks, and improve the life of rolling bearings. According to this, a proper amount of retained austenite can improve the life under foreign matter-containing lubrication, but on the other hand, there is a problem that retained austenite reduces surface hardness and fatigue resistance. It was Regarding the influence of the grain size of carbides and carbonitrides in improving the bearing life, in particular, when large carbides are repeatedly subjected to stress, the large carbides become the starting point of fatigue and cracks and flaking occur. Was not considered.

【0003】そこで、本出願人は引き続き研究を重ねた
結果、転がり表面層の残留オーステナイト量と表面硬さ
との最適な関係を見いだし、さらに、転がり表面層に存
在する炭化物,炭窒化物の平均粒径を最適な値にするこ
とで、異物混入潤滑下ばかりでなくクリーンな潤滑下で
も、従来品よりも長寿命な転がり軸受を提供するに到っ
た(特願平2−127930)。
Therefore, as a result of continuous research, the applicant of the present invention found an optimum relationship between the amount of retained austenite in the rolling surface layer and the surface hardness, and furthermore, the average grain size of carbides and carbonitrides present in the rolling surface layer. By optimizing the diameter, it has become possible to provide a rolling bearing that has a longer life than conventional products not only under lubrication containing foreign matter but also under clean lubrication (Japanese Patent Application No. 2-127930).

【0004】これは、転がり軸受の軌道輪及び転動体の
少なくとも一つを、炭化物形成元素を含有し、転がり表
面層の残留オーステナイト量(γR vol%)が20〜
45vol%、且つ、平均粒径0.5〜1.5μmの微
細炭化物又は炭窒化物の分散強化により、前記転がり表
面のビッカース硬さ(HV)が前記残留オーステナイト
量に対し、 −4.7×(γR vol%)+920≦Hv≦−4.7×(γR vol%)+1020 の範囲にある合金鋼で構成したものである。
This is because at least one of the bearing ring and rolling element of the rolling bearing contains a carbide-forming element, and the residual austenite amount (γ R vol%) of the rolling surface layer is 20 to 20.
The Vickers hardness (H V ) of the rolling surface was -4.7% with respect to the amount of retained austenite by 45 vol% and dispersion strengthening of fine carbide or carbonitride having an average particle size of 0.5 to 1.5 μm. X (γ R vol%) + 920 ≦ Hv ≦ −4.7 × (γ R vol%) + 1020.

【0005】[0005]

【発明が解決しようとする課題】しかしながら、上記従
来の転がり軸受は、平均粒径0.5〜1.5μmの微細
炭化物又は炭窒化物を確実に得ることが難しく、しばし
ば浸炭又は浸炭窒化処理において大きな初析炭化物を表
面層に局部的に生じ、これが原因してやや寿命の延長が
十分でない例がみられた。
However, it is difficult to reliably obtain fine carbides or carbonitrides having an average particle size of 0.5 to 1.5 μm in the above-mentioned conventional rolling bearings, and often in carburizing or carbonitriding treatments. In some cases, large pro-eutectoid carbides were locally generated in the surface layer, which caused a slightly insufficient life extension.

【0006】そこで本発明は、こうした従来の問題点を
解決することを課題とするものであり、実際の生産にお
いても安定的に微細な炭化物及び炭窒化物が得られ、か
つ狙いとする残留オーステナイト量及び硬さを達成し、
一層長寿命とした転がり軸受を提供することを目的とし
ている。
Therefore, the present invention has an object to solve such conventional problems, and it is possible to stably obtain fine carbides and carbonitrides in actual production and to obtain the target residual austenite. Achieves quantity and hardness,
The object is to provide a rolling bearing having a longer life.

【0007】本発明は、軌道輪及び転動体とを備えた転
がり軸受において、前記軌道輪及び転動体の少なくとも
一つの表面層は、残留オーステナイト量(γR vol
%)が20〜45vol%で、C;0.1〜1.2重量
%、Cr;1〜3重量%を含有し、さらにMoを2.0
重量%以下であって且つCr含有量の1/3以上含有す
るとともに、浸炭または浸炭窒化処理された前記表面層
表面硬さ(Hv)が前記残留オーステナイト量に対
し、−4.7×(γR vol%)+920≦Hv≦−
4.7×(γR vol%)+1020の範囲にある合金
鋼からなることを特徴とする。
According to the present invention, in a rolling bearing having a bearing ring and a rolling element, at least one surface layer of the bearing ring and the rolling element has a residual austenite content (γ R vol
%) Is 20 to 45 vol%, and C is 0.1 to 1.2 weight.
%, Cr; 1 to 3% by weight, and further contains 2.0 Mo.
The surface layer containing less than 1% by weight and not less than 1/3 of the Cr content and carburized or carbonitrided.
With respect to the surface hardness of the (Hv) is the amount of retained austenite, -4.7 × (γ R vol% ) + 920 ≦ Hv ≦ -
It is characterized by being made of an alloy steel in the range of 4.7 × (γ R vol%) + 1020.

【0008】[0008]

【作用】本発明は、1 〜3 %Cr含有鋼の浸炭および浸
炭窒化時の炭化物,炭窒化物の粒径とその量および硬
さ、残留オーステナイト量に及ぼすMo添加の効果等に
着目してなされたものである。すなわち本願発明者ら
は、残留オーステナイトの存在による表面硬さの低下を
補償する析出炭化物の微細化について研究を重ねた結
果、Cr添加量に対してMoを適切にコントロールした
量だけ加えると、析出炭化物の粒子の大きさが微細化さ
れることを見出した(Moの炭化物微細化効果)。Cr
とMoとを同時に添加した鋼の炭化物組成については未
だ明確にされていないが、Crに対するMoの量が増大
するにつれて、炭化物組成はM3 Cのセメンタイト系の
炭化物からM 236 系の合金炭化物に変わってくるもの
と思われる。セメンタイトの析出粒子は浸炭又は浸炭窒
化時におけるγ相中で他の合金炭化物より速く成長し易
いことが知られており、したがってセメンタイト系炭化
物が他の炭化物に変化したことで析出炭化物の微小化が
促進されることが、すなわち上記Moの炭化物微小化効
果をもたらすものと考えられる。このような炭化物の微
小化によって最大粒径が抑えられて、クラックの起点に
なりやすい巨大炭化物の出現が抑制されたことが、本発
明で軸受寿命の著しい延長が実現できた理由と推定され
る。
The present invention is applicable to carburizing and carburizing steel containing 1 to 3% Cr.
Grain size and amount of carbide and carbonitride during carbonitriding and hardness
The effect of Mo addition on the amount of retained austenite
It was made paying attention. That is, the present inventors
Reduces the surface hardness due to the presence of retained austenite.
The result of repeated research on the refinement of the precipitated carbides to compensate
As a result, Mo was appropriately controlled with respect to the amount of Cr added.
If only an amount is added, the size of the precipitated carbide particles becomes finer.
It was found that (carbide refining effect of Mo). Cr
The carbide composition of the steel to which Mo and Mo are added at the same time
However, the amount of Mo with respect to Cr increases.
The carbide composition is M3C cementite type
Carbide to M twenty threeC6Changed to alloy carbide
I think that the. Precipitated particles of cementite are carburized or carburized.
Easier to grow faster than other alloy carbides in the γ phase during aging
It is known that
Since the material changed to other carbides, the precipitation carbides became smaller.
It is accelerated, that is, the carbide miniaturization effect of the above Mo.
It is thought to bring fruit. Such a small amount of carbide
The maximum grain size is suppressed by miniaturization, and it becomes the starting point of cracks.
The fact that the appearance of huge carbides that are likely to occur was suppressed
It is estimated that the reason why the bearing life was remarkably extended
You.

【0009】上記炭化物が微細化する傾向は、浸炭より
も浸炭窒化の方が大きいことが実験的に認められた。こ
れは、炭化物よりも炭窒化物(Fe3 (CN))のほう
が微細化し易いこと、及び浸炭窒化温度が浸炭温度より
低いことに由来するものと考えられる。このことから、
安定した生産を実現するためには浸炭窒化のほうが望ま
しいといえる。
It has been experimentally recognized that carbonitriding has a greater tendency for the above carbides to become finer than for carburizing. It is considered that this is because carbonitride (Fe 3 (CN 3 )) is more easily refined than carbide, and the carbonitriding temperature is lower than the carburizing temperature. From this,
Carbonitriding is more desirable to achieve stable production.

【0010】また、セメンタイトはHv 1000〜1500位の
かたさであるのに対して、M236系の合金炭化物はHv
1300〜1800といわれ、この炭化物そのもののかたさ効
果と上記の微細化効果とが相まって、ころがり軸受の寿
命の延長をもたらすものと考えられる。本発明における
Moの含有量は、2.0重量%以下であって且つCr含
有量の1/3以上とする。
Cementite has a hardness of Hv 1000 to 1500, whereas M 23 C 6 alloy carbide has a hardness of Hv.
It is said to be 1300 to 1800, and it is considered that the hardness effect of the carbide itself and the above-described miniaturization effect are combined to prolong the life of the rolling bearing. The Mo content in the present invention is 2.0% by weight or less and does not include Cr.
The amount should be 1/3 or more.

【0011】Moの添加により炭化物(炭窒化物を含
む、以下同じ)の微細化を促進させるには、Moの量
、Cr含有量1〜3%を前提として、Crの量の1/
3以上必要である。この量を下回ると、Crの含有量に
対するMo量が過少となり、析出炭化物の微細化が不十
分で軸受寿命の延長効果が低い。一方Mo含有量が2%
を超えると、溶解時にMoCなどの未溶解巨大炭化物が
出現するおそれがあり、又、焼入れ温度も900°C以
上の高温を必要とし生産上からも好ましくない。
In order to promote the refinement of carbides (including carbonitrides, the same applies hereinafter) by adding Mo, the amount of Mo should be 1/3 of the amount of Cr, assuming a Cr content of 1 to 3%.
3 or more is required. When the amount is less than this amount, the amount of Mo with respect to the content of Cr becomes too small, the precipitation carbide is not refined sufficiently, and the effect of extending the bearing life is low. Hand M o content of 2%
If it exceeds, undissolved giant carbides such as MoC may appear during melting, and the quenching temperature needs to be high at 900 ° C or higher, which is not preferable from the viewpoint of production.

【0012】本発明に係る転がり軸受の合金鋼の他の特
性値の臨界的意義等について、以下に説明する。転がり
表面層の残留オーステナイト量(γR vol%);20〜
45vol%:潤滑油中等に混入する異物により、転がり
表面層に圧痕が発生する。この圧痕のエッジ部分に発生
しやすいクラックは、残留オーステナイトと密接な関係
がある。残留オーステナイトは、素材のC含有量により
多少異なるが、通常は軟らかくて粘い。従って、この残
留オーステナイトを所望の割合で転がり表面層に存在さ
せると圧痕のエッジ部分における応力集中を緩和するこ
とができ、クラックの発生を抑制することができる。ま
た、転がり表面層における残留オーステナイトは、転動
時に圧痕を通過する部材(例えば、転動体に対して軌道
輪)の相対通過回数が所定数を過ぎると、表面に加わる
変形エネルギーによりマルテンサイト変態し硬化すると
いう効果により、異物混入潤滑下での転がり軸受の寿命
を向上することができる。これらの効果を最大限発揮す
る転がり表面層における残留オーステナイト量は、20
〜45vol%である。
The critical significance of other characteristic values of the alloy steel of the rolling bearing according to the present invention will be described below. Amount of retained austenite in the rolling surface layer (γ R vol%); 20〜
45 vol%: An indentation is generated on the rolling surface layer due to a foreign substance mixed in the lubricating oil or the like. The cracks that tend to occur at the edge of the indentation are closely related to the retained austenite. Retained austenite is somewhat soft and viscous, although it varies somewhat depending on the C content of the material. Therefore, when the retained austenite is present in the rolling surface layer at a desired ratio, the stress concentration at the edge of the indentation can be reduced, and the occurrence of cracks can be suppressed. Further, the retained austenite in the rolling surface layer undergoes martensite transformation due to the deformation energy applied to the surface when the number of relative passes of the member (for example, the race ring with respect to the rolling element) that passes through the indentation during rolling exceeds a predetermined number. Due to the effect of hardening, it is possible to improve the life of the rolling bearing under lubrication containing foreign matter. The amount of retained austenite in the rolling surface layer that maximizes these effects is 20
It is about 45 vol%.

【0013】残留オーステナイト量が20vol%未満
だと前記ごみ圧痕発生の際の応力集中効果を十分発揮す
ることができない。また、残留オーステナイト量が45
vol%を越えると応力集中を緩和する効果は飽和し、
かえって表面硬さを低下することにより耐疲労性が低下
してしまう。以上の理由により、転がり表面層の残留オ
ーステナイト量は20〜45vol%、好ましくは、2
5〜40vol%とした。
If the amount of retained austenite is less than 20 vol%, the stress concentration effect at the time of dust indentation cannot be sufficiently exerted. In addition, the amount of retained austenite is 45
When it exceeds vol%, the effect of relaxing stress concentration is saturated,
On the contrary, the surface hardness is lowered, so that the fatigue resistance is lowered. For the above reasons, the amount of retained austenite in the rolling surface layer is 20 to 45 vol%, preferably 2
It was set to 5 to 40 vol%.

【0014】転がり表面層に存在する微細炭化物及び/
又は炭窒化物の平均粒径;0.5〜1.5μm :転が
り表面層の残留オーステナイト量(γR vol%)が増
えるしたがって、表面硬さ(HV )が低下する。そこ
で、本発明では、微細炭化物,炭窒化物の析出強化によ
り残留オーステナイ量に対する表面硬さを向上すること
ができる。
Fine carbides present in the rolling surface layer and /
Or average particle size of carbonitride: 0.5 to 1.5 μm: The amount of retained austenite (γ R vol%) in the rolling surface layer increases, so that the surface hardness (H V ) decreases. Therefore, in the present invention, the surface hardness with respect to the amount of retained austenite can be improved by strengthening the precipitation of fine carbides and carbonitrides.

【0015】ここで、炭化物,炭窒化物の平均粒径は、
0.5〜1.5μmである。平均粒径が0.5μm未満
だと寿命向上が不十分で、かつ、耐摩耗性が低下する。
また、平均粒径が1.5μmを越えると前記炭化物,炭
窒化物が応力の集中源となり、クラック等が発生し易く
なり転がり軸受の寿命を低下する。ところで、転がり表
面層に含有する前記微細炭化物及び炭窒化物の含有量
は、面積比で10〜30%が望ましい。炭化物,炭窒化
物が少ないと、残留オーステナイ量の増加に対する表面
硬さの低下を補償することができない。一方、これらの
量が多すぎると、炭化物が粗大化する他、マトリックス
に固溶する炭素量が低下し必要な残留オーステナイト量
を確保することができない。尚、炭化物,炭窒化物量
は、炭化物形成元素量の調整,焼戻し温度の調整等によ
り制御可能である。
Here, the average particle size of carbides and carbonitrides is
It is 0.5 to 1.5 μm. If the average particle size is less than 0.5 μm, the life is insufficiently improved and the wear resistance is reduced.
Further, if the average particle size exceeds 1.5 μm, the carbides and carbonitrides serve as a concentrated source of stress, cracks are likely to occur, and the life of the rolling bearing is shortened. By the way, the content of the fine carbides and carbonitrides contained in the rolling surface layer is preferably 10 to 30% in area ratio. When the amount of carbides and carbonitrides is small, it is not possible to compensate for the decrease in surface hardness with respect to the increase in the amount of retained austenite. On the other hand, if the amount of these is too large, the carbides are coarsened, and the amount of carbon solid-dissolved in the matrix is reduced, so that the required amount of retained austenite cannot be secured. The amounts of carbides and carbonitrides can be controlled by adjusting the amount of carbide forming elements, adjusting the tempering temperature, and the like.

【0016】炭化物形成元素としては、Cr,Mo,
V,W等公知の各種の元素がある(Wは窒化物も形成す
る)。炭窒化物は、浸炭に変えて浸炭窒化を行ったとき
の上記炭化物及びFe3 (CN)等の窒化物を言う。炭
化物形成元素として好ましいのは、Cr及びMoであ
る。Crは、鋼の焼入性及び焼戻し抵抗性を向上すると
伴に、微細な炭化物を析出して合金鋼の硬さを向上する
ために必要な炭化物形成元素である。転がり表面層に析
出する炭化物を微細化するのに適したCrの含有量は、
1〜3重量%である。Cr含有量が1重量%未満の鋼に
対し浸炭等の処理によりC濃度を高め表面硬さのみ大き
くすることは可能であるが、これでは、炭化物の核発生
が少なく炭化物が成長しやすく巨大炭化物が発生する。
Cr含有量が3重量%を越えると、素材の段階で巨大炭
化物が晶出してしまい、応力集中により寿命が低下す
る。そして、コスト的にも不利であるとともに、巨大炭
化物を微細化しようとすると炭化物をマトリックス中に
固溶して再度析出させるための熱処理,高温焼入れ等が
必要となり、熱処理生産性が低下する。
The carbide forming elements include Cr, Mo,
There are various known elements such as V and W (W also forms a nitride). Carbonitride refers to the above carbides and nitrides such as Fe 3 (CN ) when carbonitriding is performed instead of carburizing. Cr and Mo are preferable as the carbide forming element. Cr is a carbide-forming element necessary for improving the hardenability and tempering resistance of the steel and at the same time precipitating fine carbides to improve the hardness of the alloy steel. The Cr content suitable for refining the carbide precipitated in the rolling surface layer is
It is 1 to 3% by weight. Although it is possible to increase the C concentration and increase only the surface hardness of steel having a Cr content of less than 1% by weight by a treatment such as carburizing, this causes less nucleation of carbides and facilitates the growth of carbides. Occurs.
If the Cr content exceeds 3% by weight, giant carbides will crystallize at the stage of the raw material, and stress concentration will shorten the life. In addition to being disadvantageous in terms of cost, heat treatment productivity, high temperature quenching, and the like for solid-dissolving the carbide in the matrix and reprecipitating it are required to reduce the size of the giant carbide.

【0017】なお、素材を作製する方法として、鋳造の
他、公知の粉末焼結等があるが、この粉末焼結は、焼結
する際、素材の段階で巨大炭化物,炭窒化物が晶出して
しまうことがなく、好ましい方法である。Moについて
は先に述べた通りである。その他の炭化物形成元素に関
しては、例えばV;7重量%以下、特に3 重量%以下、
W;15.0重量%以下とし、それらのうち一種又は二種を
必要に応じて適宜に含有することができる。なお、微細
炭化物の析出に際しては、球状化焼鈍を行っても良い。
As a method for producing a material, there are known powder sintering and the like in addition to casting. In this powder sintering, giant carbides and carbonitrides are crystallized at the stage of the material during sintering. This is a preferable method because it does not occur. Mo is as described above. Regarding other carbide-forming elements, for example, V: 7% by weight or less, particularly 3% by weight or less,
W; 15 .0 and wt% or less, it may be contained in as necessary one or two or of them. Note that spheroidizing annealing may be performed when precipitating fine carbides.

【0018】転がり表面層の硬さ(HV )が転がり表面
層の残留オーステナイト量(γR vol%)に対し、 −4.7×(γR vol%)+920≦Hv≦−4.7×(γR vol%)+1020 :本発明では、各残留オーステナイト量に対応する硬さ
範囲を上式で示す範囲内にした。
The hardness (H V ) of the rolling surface layer is −4.7 × (γ R vol%) + 920 ≦ Hv ≦ −4.7 × with respect to the residual austenite amount (γ R vol%) of the rolling surface layer. (Γ R vol%) + 1020: In the present invention, the hardness range corresponding to each retained austenite amount is set within the range shown by the above formula.

【0019】上式の関係において、硬さが前記下限値よ
り小さいと、耐疲労性が低下し、異物混入潤滑下及びク
リーンの潤滑下でも寿命が低下する。一方、硬さを前記
上限値より大きくすることは困難である。本発明に使用
する合金鋼としては、肌焼鋼,高炭素クロム軸受鋼,高
温軸受用高速度鋼を使用することができ、その炭素含有
量は0.1 〜1.0 重量%の範囲である。炭素含有量を0.1
重量%以上としたのは、製鋼上これより少なくすること
が困難なためである。
In the relationship of the above equation, if the hardness is less than the lower limit value, the fatigue resistance is lowered, and the life is shortened even under the contamination with foreign matter and the lubrication of clean. On the other hand, it is difficult to make the hardness higher than the upper limit value. As the alloy steel used in the present invention, case hardening steel, high carbon chromium bearing steel and high speed bearing high speed steel can be used, and the carbon content thereof is in the range of 0.1 to 1.0% by weight. Carbon content 0.1
The reason why the content is set to be at least wt% is that it is difficult to reduce the amount in terms of steelmaking.

【0020】一方、炭素含有量が1.2 重量%を越える
と、素材の段階で巨大な炭化物が発生しやすくなるた
め、靱性が低下し、破壊強度も低下する危険が生じるた
め上限を1.2 重量%とした。
On the other hand, if the carbon content exceeds 1.2% by weight, huge carbides are likely to be generated at the stage of the raw material, and the toughness and the fracture strength are lowered. Therefore, the upper limit is set to 1.2% by weight. did.

【0021】[0021]

【実施例】次に、本発明の実施例を説明する。表1に示
すような組成の鋼を材料とする試験片について、次のよ
うに浸炭熱処理を行った。
Next, embodiments of the present invention will be described. Carburizing heat treatment was performed on the test pieces made of steel having the composition shown in Table 1 as follows.

【0022】[0022]

【表1】 [Table 1]

【0023】すなわち、各試験片の浸炭熱処理のうちダ
イレクト焼入れは、図1に示すグラフのように、RX
ス+エンリッチガスの雰囲気で、約3〜5時間、920
〜960℃で熱処理を行い、常温まで空冷し、次いで8
40℃×1時間の油焼入れを行い、更に180℃×2時
間の焼戻しを行った。また、浸炭窒化熱処理について
は、図2のグラフに示すように、RX ガス+エンリッチ
ガス+アンモニアガス5%の雰囲気で、約3〜5時間、
880℃で浸炭窒化熱処理を行い、油冷してその後、上
記浸炭処理の場合と同様な処理を行った。
That is, the direct quenching of the carburizing heat treatment of each test piece is performed at 920 for about 3 to 5 hours in an atmosphere of R X gas + enriched gas as shown in the graph of FIG.
Heat treatment at ~ 960 ° C, air cool to room temperature, then 8
Oil quenching was performed at 40 ° C. for 1 hour, and further tempering was performed at 180 ° C. for 2 hours. As for the carbonitriding heat treatment, as shown in the graph of FIG. 2, with R X gas + enriched gas + ammonia gas 5% atmosphere of about 3-5 hours,
Carbonitriding heat treatment was performed at 880 ° C., oil cooling was performed, and then the same treatment as in the case of the above carburizing treatment was performed.

【0024】次いで上記浸炭熱処理後の各試験片につい
て、残留オーステナイト量,表面硬さ,炭化物の平均粒
径と最大粒径の測定を測定した。なお、残留オーステナ
イト量はX線分析法によって行い、炭化物の粒径の測定
は顕微鏡法によった。更に、上記浸炭熱処理後の各試験
片を用いて転がり軸受の内輪及び外輪のいずれにも適用
できる円板状試験片を作成し、『特殊鋼便覧』(第1
版,電気製鋼研究所編,理工学社,1969年5月25
日)第10〜21頁記載のスラスト形軸受鋼試験機を用
いてスラスト寿命試験を行った。試験条件は次の通りで
ある。
Then, the amount of retained austenite, the surface hardness, the average particle size of the carbide and the maximum particle size of each test piece after the above carburizing heat treatment were measured. The amount of retained austenite was measured by X-ray analysis, and the grain size of carbide was measured by microscopy. Further, a disk-shaped test piece applicable to both the inner ring and the outer ring of the rolling bearing was prepared by using each of the test pieces after the carburizing heat treatment as described in "Special Steel Handbook" (No. 1).
Edition, Electric Steel Research Institute, Riko Engineering, May 25, 1969
Sun) A thrust life test was performed using a thrust bearing steel tester described on pages 10 to 21. The test conditions are as follows.

【0025】N=1000rpm Pmax =500Kgf/mm2 潤滑油 #68タービン油 なお、ゴミとして鋼粉(硬さHV =870,径74〜1
47μmのFe3 C)を潤滑油中に300ppm 混入し
た。
N = 1000 rpm P max = 500 Kgf / mm 2 Lubricating oil # 68 Turbine oil Steel dust (hardness H V = 870, diameter 74-1)
47 μm of Fe 3 C) was mixed in the lubricating oil at 300 ppm.

【0026】寿命判定は、各試験片についてその10%
に顕微鏡又は肉眼で視認できるクラック,フレーキング
が発生した時点を寿命(L10寿命)とし、この時点迄の
累積回転数をもって寿命を定量的に表現した。これらの
試験結果を表1に併せて示し、残留オーステナイト量と
表面硬さとの関係を図3に、Cr含有量とMo含有量と
の関係を図4に示す。表1において、試験片1〜5は本
発明の実施例に相当するものであり、そのCr,Mo
量は請求項1の範囲内にある。
10% of the life of each test piece was judged.
The life (L 10 life) was defined as the time when cracks and flaking were observed with a microscope or the naked eye, and the life was quantitatively expressed by the cumulative number of revolutions up to this time. The test results shows in Table 1., and the amount of retained austenite
Fig. 3 shows the relationship between the surface hardness and the Cr content and the Mo content.
Shows the relationship in Figure 4. In Table 1, test pieces 1 to 5 correspond to the examples of the present invention, and their Cr and Mo contents are included.
Yes amount is in the range of claim 1.

【0027】試験片6以降は本発明の比較例である。そ
のうち試験片6〜10は、先の出願(特願平2−127
930)の発明の範囲内にあるが、ただしMo添加量が
Cr添加量の 1/3未満であり、本発明の範囲を下回って
いるものである。試験片11〜15は、Mo添加量がC
r添加量の 1/3未満で、且つ表面硬さが本発明の範囲外
のものである。
The test pieces 6 and the following are comparative examples of the present invention. Among them, test pieces 6 to 10 were previously applied (Japanese Patent Application No. 2-127).
930), but the amount of Mo added is less than 1/3 of the amount of Cr added, which is below the range of the present invention. The test pieces 11 to 15 have a Mo addition amount of C.
It is less than 1/3 of the added amount of r and the surface hardness is out of the range of the present invention.

【0028】試験片16〜19は、Mo添加量,残留オ
ーステナイト量,表面硬さのいずれも本発明の範囲外の
ものである。表1から明らかなように、本発明の試験片
1〜5のものは、全て炭化物粒径なかでも最大粒径が比
較例に比し目立って小さくなっており、寿命の延長効果
が顕著に認められる。
In the test pieces 16 to 19, the Mo addition amount, the retained austenite amount, and the surface hardness are all outside the scope of the present invention. As is clear from Table 1, in all of the test pieces 1 to 5 of the present invention, the maximum particle size among all the carbide particle sizes was remarkably smaller than that of the comparative example, and the effect of extending the life was remarkably recognized. To be

【0029】これに対して、比較例の試験片6〜10の
ものは、炭化物平均粒径が本発明のものと同程度であっ
てもその最大粒径は本発明のそれを大幅に上回ってお
り、寿命は上記本発明のものに比べると1/2 〜1/3 以下
に過ぎない。比較例の試験片11〜15のものは、炭化
物平均粒径のばらつきが大きく、最大粒径も更に大きく
なっており、一方、寿命は上記試験片6〜10のものよ
り更に短いことが認められる。
On the other hand, in the test pieces 6 to 10 of the comparative examples, the maximum particle size is much larger than that of the present invention even though the average particle size of the carbides is similar to that of the present invention. The life is only 1/2 to 1/3 or less as compared with that of the present invention. It is recognized that the test pieces 11 to 15 of the comparative examples have large variations in the average particle size of the carbides and the maximum particle size is larger, while the lifespan is shorter than that of the test pieces 6 to 10. .

【0030】比較例の試験片16〜19のものは、炭化
物最大粒径が上記試験片11〜15に比し小さい傾向を
示しているにもかかわらず、炭化物平均粒径の方はかな
り大きな値を示していて、寿命は最も短くなっている。
なお、本実施例では、表1に示す組成の鋼を材料とする
試験片1〜5を用いたが、この成分は一例であり、他の
成分組成の鋼を用いても良い。
The test pieces 16 to 19 of the comparative examples have a tendency that the maximum particle size of carbides is smaller than that of the test pieces 11 to 15, but the average particle size of the carbides is considerably larger. , The life is the shortest.
In addition, in this example, the test pieces 1 to 5 made of steel having the composition shown in Table 1 were used, but this component is an example, and steel having other component compositions may be used.

【0031】また、本実施例では浸炭方法としてガス浸
炭を行った場合を示したが、これに限らずイオン浸炭を
行ってもよい。
In this embodiment, gas carburizing is used as the carburizing method, but the present invention is not limited to this, and ion carburizing may be performed.

【0032】[0032]

【発明の効果】以上説明したように本発明によれば、C
r添加量に対するMo添加量を所定の範囲に制御するこ
とにより、炭化物粒径の微細化を促進せしめて、異物混
入潤滑下にあっても長寿命な転がり軸受を提供すること
ができるという効果が得られる。
As described above, according to the present invention, C
By controlling the amount of addition of Mo with respect to the amount of addition of r within a predetermined range, it is possible to promote the miniaturization of the carbide grain size and provide a rolling bearing having a long life even under the contamination with foreign matter. can get.

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

【図1】本発明に係る転がり軸受を製造するための浸炭
熱処理条件を説明する工程図である。
FIG. 1 is a process chart illustrating carburizing heat treatment conditions for manufacturing a rolling bearing according to the present invention.

【図2】本発明に係る転がり軸受を製造するための浸炭
窒化熱処理条件を説明する工程図である。
FIG. 2 is a process chart illustrating carbonitriding heat treatment conditions for manufacturing a rolling bearing according to the present invention.

【図3】FIG. 3 本発明の残留オーステナイト量と表面硬さとのOf the amount of retained austenite and the surface hardness of the present invention
関係を示す特性図である。It is a characteristic view which shows a relationship.

【図4】FIG. 4 本発明のCr含有量とMo含有量との関係を示The relationship between the Cr content and the Mo content of the present invention is shown.
す特性図である。FIG.

───────────────────────────────────────────────────── フロントページの続き (51)Int.Cl.6 識別記号 庁内整理番号 FI 技術表示箇所 // C22C 38/00 301 C22C 38/00 301Z 38/22 38/22 ─────────────────────────────────────────────────── ─── Continuation of the front page (51) Int.Cl. 6 Identification code Office reference number FI technical display location // C22C 38/00 301 C22C 38/00 301Z 38/22 38/22

Claims (2)

(57)【特許請求の範囲】(57) [Claims] 【請求項1】 軌道輪及び転動体とを備えた転がり軸受
において、前記軌道輪及び転動体の少なくとも一つの表
面層は、残留オーステナイト量(γR vol%)が20
〜45vol%で、C;0.1〜1.2重量%、Cr;
1〜3重量%を含有し、さらにMoを2.0重量%以下
であって且つCr含有量の1/3以上含有するととも
に、浸炭または浸炭窒化処理された前記表面層の表面硬
さ(Hv)が前記残留オーステナイト量に対し、−4.
7×(γR vol%)+920≦Hv≦−4.7×(γ
R vol%)+1020の範囲にある合金鋼からなるこ
とを特徴とする転がり軸受。
1. A rolling bearing provided with a bearing ring and a rolling element, wherein at least one table of the bearing ring and the rolling element is provided.
The surface layer has a residual austenite amount (γ R vol%) of 20.
~ 45 vol%, C; 0.1-1.2 wt%, Cr;
1 to 3% by weight, and 2.0% by weight or less of Mo
And the surface hardness (Hv) of the surface layer that is 1/3 or more of the Cr content and is carburized or carbonitrided with respect to the residual austenite amount.
7 × (γ R vol%) + 920 ≦ Hv ≦ −4.7 × (γ
A rolling bearing characterized by being made of an alloy steel in the range of ( R vol%) + 1020.
【請求項2】 微細炭化物又は炭窒化物の最大粒径が
2.3μm以下である請求項1記載の転がり軸受。
2. The rolling bearing according to claim 1, wherein the maximum grain size of the fine carbide or carbonitride is 2.3 μm or less.
JP3178191A 1991-07-18 1991-07-18 Rolling bearing Expired - Lifetime JP2541160B2 (en)

Priority Applications (3)

Application Number Priority Date Filing Date Title
JP3178191A JP2541160B2 (en) 1991-07-18 1991-07-18 Rolling bearing
GB9215243A GB2258274B (en) 1991-07-18 1992-07-17 Rolling bearing
US08/134,588 US5427457A (en) 1991-07-18 1993-10-12 Rolling bearing

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP3178191A JP2541160B2 (en) 1991-07-18 1991-07-18 Rolling bearing

Publications (2)

Publication Number Publication Date
JPH0525609A JPH0525609A (en) 1993-02-02
JP2541160B2 true JP2541160B2 (en) 1996-10-09

Family

ID=16044188

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Country Link
JP (1) JP2541160B2 (en)
GB (1) GB2258274B (en)

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JPH0788851B2 (en) * 1987-08-25 1995-09-27 日本精工株式会社 Rolling bearing
KR930010411B1 (en) * 1988-07-11 1993-10-23 니혼 세이코오 가부시끼가이샤 Rolling bearing
JPH0826446B2 (en) * 1990-05-17 1996-03-13 日本精工株式会社 Rolling bearing

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Publication number Priority date Publication date Assignee Title
US8083868B2 (en) 2004-01-20 2011-12-27 Nsk Ltd Rolling bearing

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JPH0525609A (en) 1993-02-02
GB2258274B (en) 1995-06-21
GB2258274A (en) 1993-02-03
GB9215243D0 (en) 1992-09-02

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