JP2004278781A - Rolling bearing, and manufacturing method for the same - Google Patents

Rolling bearing, and manufacturing method for the same Download PDF

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JP2004278781A
JP2004278781A JP2004002791A JP2004002791A JP2004278781A JP 2004278781 A JP2004278781 A JP 2004278781A JP 2004002791 A JP2004002791 A JP 2004002791A JP 2004002791 A JP2004002791 A JP 2004002791A JP 2004278781 A JP2004278781 A JP 2004278781A
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rolling
temperature
rolling bearing
nitrogen
carbonitriding
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Tsutomu Oki
力 大木
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NTN Corp
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NTN Corp
NTN Toyo Bearing Co Ltd
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Abstract

<P>PROBLEM TO BE SOLVED: To provide a rolling bearing capable of suppressing hydrogen embrittlement separation occurring under hydrogen environment, and a manufacturing method for the same. <P>SOLUTION: At least one component of a rolling element 2, an inner ring 4 and an outer ring 3 of the rolling bearing as a bearing 1 for an alternator has a nitrogen enriched layer, and the area ratio of spheroidal carbide of a face layer part is ≥ 10%. <P>COPYRIGHT: (C)2005,JPO&NCIPI

Description

本発明はころがり軸受およびその製造方法に関し、より具体的には水素の発生する環境下で白層を伴なう水素脆性剥離を生じにくいころがり軸受およびその製造方法に関するものである。   The present invention relates to a rolling bearing and a method for manufacturing the same, and more specifically to a rolling bearing and a method for manufacturing the same that are less likely to cause hydrogen embrittlement with a white layer in an environment where hydrogen is generated.

オルタネータ軸受、建設機械用減速機、油圧ポンプ、油圧モータ等に用いられるころがり軸受では、損傷起点に白層を伴なった特異な剥離部が認められる場合が多い。この白層の形態は、転動疲労によって生じるWEC(White Etching Constituent)や非金属介在物周りに発生するバタフライとは異なり、転動方向に対して方向性を持たないことが特徴である。起点に白層を含む損傷が発生した軸受では、明らかに鋼中水素量が増加しており、白層内に存在する亀裂が結晶粒界に沿って非常に長く内部にまで進展している。このため、上記損傷の発生に水素が関与しているとされている。以後、この白層を伴なう特異な剥離を水素脆性剥離と称する。   Rolling bearings used in alternator bearings, reduction gears for construction machinery, hydraulic pumps, hydraulic motors, and the like often have a peculiar peeling portion with a white layer at the damage starting point. This white layer is characterized by having no directionality in the rolling direction, unlike a white etching constituent (WEC) generated by rolling fatigue or a butterfly generated around nonmetallic inclusions. In a bearing having a damage including a white layer at the starting point, the hydrogen content in the steel is clearly increased, and the cracks existing in the white layer extend very long along the grain boundaries to the inside. For this reason, it is said that hydrogen is involved in the generation of the damage. Hereinafter, the peculiar peeling with the white layer is referred to as hydrogen embrittlement peeling.

水素脆性剥離は転動時に発生した化学的に活性な金属新生面の触媒作用で潤滑剤が分解し、発生した水素が鋼中に侵入することにより生じると考えられる。そのため、水素脆性剥離の対策として、(a1)化学的に分解しにくい潤滑剤への変更や、(a2)金属新生面を出にくくする黒染処理などが有効とされてきた。   It is considered that the hydrogen embrittlement peeling is caused by the decomposition of the lubricant by the catalytic action of the chemically active new metal surface generated during rolling and the generated hydrogen penetrating into the steel. Therefore, as measures against hydrogen embrittlement peeling, it has been effective to (a1) change to a lubricant which is hardly decomposed chemically, and (a2) blackening treatment which makes it difficult for a new metal surface to appear.

上記の(a1)に関して、次のような軸受の提案がなされている。アルキルジフェニルエーテル油とポリαオレフィン油を、20:80〜80:20の重量比で配合した基油に、増稠剤として芳香族ジウレア化合物、または芳香族ウレア・ウレタン化合物を5〜40重量%配合し、さらに不動態化酸化剤および有機スルホン酸塩を添加したグリース組成物をころがり軸受内に封入してなるオルタネータ用グリース封入軸受(特許文献1)。   Regarding the above (a1), the following bearings have been proposed. 5 to 40% by weight of an aromatic diurea compound or an aromatic urea / urethane compound as a thickener is added to a base oil in which an alkyl diphenyl ether oil and a poly-α-olefin oil are mixed in a weight ratio of 20:80 to 80:20. A grease-enclosed bearing for an alternator in which a grease composition further containing a passivating oxidizing agent and an organic sulfonate is enclosed in a rolling bearing (Patent Document 1).

また、上記(a2)に関して、次のような軸受の提案がなされている。軸受内にグリースを封入したグリース封入軸受において、軌道輪の転走面に厚さ0.1〜2.5μmの酸化皮膜を形成したグリース封入軸受(特許文献2)。   With respect to the above (a2), the following bearings have been proposed. A grease-sealed bearing in which grease is sealed in a bearing, wherein a 0.1 to 2.5 μm-thick oxide film is formed on a rolling surface of a bearing ring (Patent Document 2).

上記の提案に基づく軸受は、この業界において実際に延命効果が確認されている。
特開平5−263091号公報 特開平2−190615号公報
Bearings based on the above proposals have actually been confirmed to have a life extension effect in this industry.
JP-A-5-263091 JP-A-2-190615

しかし、近年、ころがり軸受の使用環境が益々苛酷化しており、上記対策だけでは不十分な場合が生じてきた。このため、水素脆性剥離寿命のさらなる延命対策が求められている。   However, in recent years, the use environment of rolling bearings has become increasingly severe, and the above measures alone have been insufficient. For this reason, there is a demand for measures to further extend the life of hydrogen embrittlement peeling.

本発明は、水素環境下で発生する上記水素脆性剥離を抑制することができるころがり軸受およびその製造方法を提供することを目的とする。   An object of the present invention is to provide a rolling bearing capable of suppressing the hydrogen embrittlement peeling generated in a hydrogen environment and a method for manufacturing the rolling bearing.

本発明のころがり軸受は、転動体、内輪および外輪のうちの少なくとも1つの部材が窒素富化層を有し、その窒素富化層を有する部材の表層部における球状化炭化物の面積率が10%以上である。   In the rolling bearing of the present invention, at least one of the rolling element, the inner ring and the outer ring has a nitrogen-enriched layer, and the area ratio of the spheroidized carbide in the surface layer portion of the member having the nitrogen-enriched layer is 10%. That is all.

窒素富化層は、転動疲労現象を遅延させることができ、さらに表層部の球状化炭化物の面積率を10%以上とすることにより、水素脆性剥離を抑制することができる。なお、上記窒素富化層は、あとで説明するように、浸炭窒化処理により形成されるが、上記窒素富化層に炭素が富化されていてもよいし、富化されていなくてもよい。   The nitrogen-enriched layer can delay the rolling fatigue phenomenon, and can suppress hydrogen embrittlement exfoliation by setting the area ratio of the spheroidized carbide in the surface layer portion to 10% or more. Note that the nitrogen-enriched layer is formed by carbonitriding as described later, but the nitrogen-enriched layer may or may not be enriched with carbon. .

上記の水素脆性剥離を生じやすい使用態様の一例として、前記部材が密閉され、その密閉された中で水素が発生され、水素分圧が、一般のころがり軸受を形成する鋼材に水素が侵入するしきい値以上に高くなる環境での使用を挙げることができる。   As an example of a usage mode in which the above-described hydrogen embrittlement is likely to occur, the member is sealed, hydrogen is generated in the sealed portion, and a hydrogen partial pressure is generated, and hydrogen invades steel material forming a general rolling bearing. Use in an environment where the temperature is higher than the threshold value can be mentioned.

上記の水素環境下では、通常の鋼材では水素が侵入する。その侵入した水素は、転動荷重によって発生した転位が高密度に集積する部位や、非金属介在物などの部位に集合する。集合した水素は、気体分子になろうとして微小部に異常な高圧部を形成し、白層を形成し、水素脆性剥離の起点となると考えられる。上記の本発明に係るころがり軸受の部材では、水素侵入を抑制し、また、水素の集合を妨げることができる。このため、白層の形成を容易に生じさせず、水素脆性剥離を抑制することができる。   Under the above-described hydrogen environment, hydrogen invades normal steel. The penetrated hydrogen collects at a site where dislocations generated by the rolling load accumulate at a high density or at a site such as a nonmetallic inclusion. It is considered that the collected hydrogen forms an abnormal high-pressure part in a minute part to become a gas molecule, forms a white layer, and becomes a starting point of hydrogen embrittlement separation. In the above-described member of the rolling bearing according to the present invention, hydrogen intrusion can be suppressed, and aggregation of hydrogen can be prevented. For this reason, formation of a white layer does not easily occur, and hydrogen embrittlement separation can be suppressed.

なお、球状化炭化物の面積率は、通常の試験方法、たとえば市販の光学顕微鏡や走査型電子顕微鏡などの顕微鏡組織から、市販の面積率測定装置を用いて容易に求めることができる。この面積率は、数視野において求めて平均化することが望ましい。   The area ratio of the spheroidized carbide can be easily obtained from a normal test method, for example, a microstructure such as a commercially available optical microscope or scanning electron microscope using a commercially available area ratio measuring device. It is desirable that the area ratio is obtained and averaged in several visual fields.

また、上記窒素富化層を有し、且つ、その球状化炭化物が面積率の10%以上を有する部材のオーステナイト結晶粒界の粒度番号が10番を超えるとしてもよい。オーステナイト粒径をこのように微細にすることにより、窒素富化層との組み合わせにより、飛躍的に水素脆性剥離を抑制する効果が向上する。なお、上記のオーステナイト結晶粒界の平均粒径の閾値は、窒素富化層において満たされればよい。しかし、通常の場合、窒素富化層より内側の鋼材本体においても、上記のオーステナイト結晶粒微細化の基準は満たされる。また、オーステナイト粒という場合、焼入れられた後のマルテンサイトやベイナイトなどのフェライト相にその痕跡を残している。焼入れ前のオーステナイト粒界を強調するために「旧」を付する場合もある。すなわち、オーステナイト粒と旧オーステナイト粒とは同じものを表現している。なお、上記オーステナイト結晶粒は、対象とする部材の金相試料に対してエッチングなど、粒界を顕出する処理を施して観察することができる粒界である。低温焼入れ直前の加熱された時点での粒界という意味で、上記のように旧オーステナイト粒と呼ぶ場合がある。測定は、JIS規格の粒度番号の平均値から平均粒径に換算して求めてもよいし、切片法などにより金相組織に重ねたランダム方向の直線が粒界と会合する間の間隔長さの平均値をとってもよい。   Further, the member having the nitrogen-enriched layer and having the spheroidized carbide having an area ratio of 10% or more may have a grain size number of an austenite crystal grain boundary exceeding number 10. By reducing the austenite particle size in this way, the effect of dramatically suppressing hydrogen embrittlement exfoliation is improved by combination with the nitrogen-enriched layer. Note that the threshold value of the average grain size of the austenite grain boundaries described above may be satisfied in the nitrogen-enriched layer. However, in the normal case, the above criteria for refining austenite crystal grains are satisfied even in the steel material body inside the nitrogen-enriched layer. In the case of austenite grains, traces are left on the ferrite phase such as martensite or bainite after quenching. "Old" may be added to emphasize austenite grain boundaries before quenching. That is, the austenite grains and the former austenite grains express the same thing. The austenite crystal grains are grain boundaries that can be observed by performing a process such as etching on a gold phase sample of a target member to reveal the grain boundaries. As described above, it may be referred to as old austenite grains in the sense of a grain boundary at the time of heating immediately before low-temperature quenching. The measurement may be performed by converting the average value of the particle size numbers of the JIS standard into the average particle size, or the length of the interval between the lines in the random direction superimposed on the metal phase structure by the intercept method or the like and meeting the grain boundary. May be averaged.

本発明のころがり軸受の製造方法は、転動体、内輪および外輪を含むころがり軸受の製造方法であって、転動体、内輪および外輪のうちの少なくとも1つの部材を形成する鋼材を、A1点以上の温度に加熱して1.3〜1.6のCP(Carbon Potential)値で浸炭窒化処理した後、A1点より低い温度に油冷する。   A method for manufacturing a rolling bearing of the present invention is a method for manufacturing a rolling bearing including a rolling element, an inner ring, and an outer ring, wherein a steel material forming at least one member of the rolling element, the inner ring, and the outer ring is subjected to A1 points or more. After heating to a temperature and carbonitriding at a CP (Carbon Potential) value of 1.3 to 1.6, the mixture is oil-cooled to a temperature lower than the A1 point.

本発明の別のころがり軸受の製造方法は、転動体、内輪および外輪を含むころがり軸受の製造方法であって、転動体、内輪および外輪のうちの少なくとも1つの部材を形成する鋼材を、A1点以上の温度に加熱して浸炭窒化処理した後、A1点より低い温度に冷却し、次いでA1点以上の温度であって、浸炭窒化処理の温度未満の焼入れ温度域に再加熱し、焼入れする。   Another method for manufacturing a rolling bearing of the present invention is a method for manufacturing a rolling bearing including a rolling element, an inner ring, and an outer ring, wherein a steel material forming at least one member of the rolling element, the inner ring, and the outer ring is A1 point. After heating to the above temperature and performing the carbonitriding treatment, it is cooled to a temperature lower than the A1 point, and then reheated to a quenching temperature range not lower than the temperature of the A1 point and less than the temperature of the carbonitriding treatment, and quenched.

このように製造されることにより、上記のように、所定の球状化炭化物の面積率基準を満たす窒素富化層を表層部に有し、オーステナイト結晶粒の上記微細化の基準を満たした部材を得ることができる。   By being manufactured in this manner, as described above, a member having a nitrogen-enriched layer that satisfies a predetermined area ratio standard of spheroidized carbide in the surface layer portion and a member that satisfies the standard for miniaturization of austenite crystal grains is used. Obtainable.

図1は、本発明の実施の形態におけるオルタネータ用軸受を示す図である。オルタネータ10において、オルタネータ用軸受1にシャフト11が挿入され、突き出た端部にプーリ5が取り付けられている。プーリ5には、伝動ベルトが掛けられる係合溝6が設けられる。オルタネータ用軸受1は、転走面において転動体である鋼球2と接触する内輪4および外輪3を備え、鋼球は内輪と外輪との間で保持器7によって保持されている。   FIG. 1 is a diagram showing an alternator bearing according to an embodiment of the present invention. In the alternator 10, the shaft 11 is inserted into the alternator bearing 1, and the pulley 5 is attached to the protruding end. The pulley 5 is provided with an engagement groove 6 on which a transmission belt is hung. The alternator bearing 1 includes an inner ring 4 and an outer ring 3 which are in contact with steel balls 2 as rolling elements on a rolling surface, and the steel balls are held by a retainer 7 between the inner ring and the outer ring.

近年の高速化、小型化の傾向を反映して、シャフト11は伝動ベルトにより高速回転され、転動体2と軌道輪3,4とは高面圧で、高速の接触をする。オルタネータ軸受にはグリースが封入されているが、このグリースは上記高圧、高速の接触部において分解され、水素を発生する。水素は、小さい元素であり、水素分圧と表層部との条件が適合すれば鋼材中に容易に侵入する。このため、荷重が負荷されている鋼材中の所定の箇所に損傷を生じ、その破面上に白層として表れる特異な割れを形成するにいたる。   The shaft 11 is rotated at a high speed by the transmission belt, and the rolling elements 2 and the bearing rings 3 and 4 make high-speed contact with each other at a high surface pressure, reflecting the recent trend of high speed and miniaturization. Grease is sealed in the alternator bearing, and this grease is decomposed at the high-pressure, high-speed contact portion to generate hydrogen. Hydrogen is a small element, and easily penetrates into steel when the conditions of the hydrogen partial pressure and the surface layer are met. For this reason, damage is caused at a predetermined location in the steel material to which the load is applied, resulting in formation of a unique crack appearing as a white layer on the fracture surface.

本発明の実施の形態におけるオルタネータ用軸受では、転動体2、外輪3および内輪4のうちの少なくとも1つの部材が、次の2つの要件のいずれかを備える。
(A1):窒素富化層を有し、かつ、表層部の球状化炭化物の面積率が10%以上であること。
(A2):(A1)に加えて、オーステナイト結晶粒がJISに規定される粒度番号で10番以上であること。
In the alternator bearing according to the embodiment of the present invention, at least one of the rolling elements 2, the outer ring 3 and the inner ring 4 has one of the following two requirements.
(A1): It has a nitrogen-enriched layer, and the area ratio of the spheroidized carbide in the surface layer portion is 10% or more.
(A2): In addition to (A1), the austenite crystal grains have a grain size number of 10 or more specified by JIS.

上記の2つの要件のいずれかを備えた部材は、水素脆性剥離を生じ難くなり、長寿命を得ることができる。   A member satisfying any of the above two requirements is less likely to cause hydrogen embrittlement separation, and can have a long life.

次に、実際に上記のことを検証した実施例について説明する。   Next, an example in which the above is actually verified will be described.

(実施例)
上述の水素脆性剥離を発生しにくくさせる本発明例の鋼材として、図2(a)〜(b)に示す2種類の処理を施したSUJ2を準備した。
(Example)
As a steel material of the example of the present invention that hardly causes the above-mentioned hydrogen embrittlement separation, SUJ2 subjected to two kinds of treatments shown in FIGS. 2A and 2B was prepared.

図2(a)に示す本発明例1の処理では、1.3〜1.6という高いCP(Carbon Potential)値で浸炭窒化処理を行なった後に、その温度から油冷により焼き入れる。このような高いCP値の雰囲気で浸炭窒化処理することにより、表層部における球状化炭化物の面積率を確実に10%以上にすることができる。
その後、180℃で焼き戻す。
In the process of Example 1 of the present invention shown in FIG. 2A, after performing carbonitriding at a high CP (Carbon Potential) value of 1.3 to 1.6, quenching is performed by oil cooling from that temperature. By performing carbonitriding in an atmosphere having such a high CP value, the area ratio of the spheroidized carbide in the surface layer portion can be reliably increased to 10% or more.
Thereafter, it is tempered at 180 ° C.

図2(b)に示す本発明例2の処理では、比較例1(図2(c)参照)における浸炭窒化処理および焼入処理の後に、A℃(845℃)−α℃という最初の焼入れ温度よりα℃低い温度に加熱して油焼入れする。この(A−α)℃という温度は、A1点以上であって、その前の浸炭窒化処理および焼入温度より低い温度である。図示しているように、浸炭窒化処理の温度から焼入れを行なうので、焼入れ温度と浸炭窒化処理温度とは同じである。本説明において、この(A−α)℃に加熱して焼き入れる処理を低温焼入れと呼ぶこととする。この低温焼入れの後、180℃で焼き戻す。   In the treatment of Example 2 of the present invention shown in FIG. 2B, after the carbonitriding treatment and the quenching treatment in Comparative Example 1 (see FIG. 2C), the first quenching of A ° C. (845 ° C.)-Α ° C. was performed. The oil is quenched by heating to a temperature lower than α ° C. The temperature (A-α) ° C. is a temperature not lower than the A1 point and lower than the preceding carbonitriding and quenching temperatures. As shown in the figure, quenching is performed from the temperature of the carbonitriding process, so that the quenching temperature and the carbonitriding temperature are the same. In the present description, the process of heating and quenching at (A-α) ° C. is referred to as low-temperature quenching. After this low-temperature quenching, it is tempered at 180 ° C.

上記の熱処理のどちらによっても、その中の浸炭窒化処理により「浸炭窒化処理層」である窒素富化層が形成される。浸炭窒化処理において素材となる鋼の炭素濃度が高いため、通常の浸炭窒化処理の雰囲気から炭素が鋼の表面に侵入しにくい場合がある。たとえば炭素濃度が高い鋼の場合(1wt%程度の鋼)、それ以上高い炭素濃度の浸炭層が生成する場合もあるし、それ以上高い炭素濃度の浸炭層は生成しにくい場合がある。しかし、窒素濃度は、Cr濃度などにも依存するが、通常の鋼では最大限0.025wt%程度以下と低いので、素材の鋼の炭素濃度によらず窒素富化層が明瞭に生成される。上記窒素富化層には炭素が富化されていてもよいことはいうまでもない。   In any of the above heat treatments, a carbon-nitriding treatment therein forms a nitrogen-enriched layer that is a “carbonitriding treatment layer”. Since the carbon used as the material in the carbonitriding process has a high carbon concentration, carbon may not easily enter the surface of the steel from the atmosphere of the normal carbonitriding process. For example, in the case of steel having a high carbon concentration (steel of about 1 wt%), a carburized layer having a higher carbon concentration may be generated, and a carburized layer having a higher carbon concentration may be hardly generated. However, although the nitrogen concentration depends on the Cr concentration, etc., it is as low as 0.025 wt% or less at maximum in ordinary steel, so that a nitrogen-enriched layer is clearly formed regardless of the carbon concentration of the material steel. . It goes without saying that the nitrogen-enriched layer may be enriched with carbon.

また、比較例の鋼材として、図2(c)に示す処理を施したSUJ2、SUJ2の普通焼入材、SUJ2黒染処理材、13%Cr鋼の4つの鋼材を用いて、比較のための評価を行なった。表1に評価を行なった鋼材の一覧を示す。   Further, as steel materials of the comparative example, four steel materials of SUJ2, a normally quenched material of SUJ2, a SUJ2 blackened material, and a 13% Cr steel subjected to the treatment shown in FIG. An evaluation was performed. Table 1 shows a list of the steel materials evaluated.

Figure 2004278781
Figure 2004278781

図3に、水素脆性剥離の寿命を評価するのに用いた試験機を示す。この評価試験に用いた試験体の軸受は、外径32mm×内径24mm×長さ19.8mmのラジアルニードル軸受である。上記試験における試験条件を表2に示す。   FIG. 3 shows a tester used to evaluate the life of hydrogen embrittlement delamination. The bearing of the test body used in this evaluation test is a radial needle bearing having an outer diameter of 32 mm, an inner diameter of 24 mm, and a length of 19.8 mm. Table 2 shows the test conditions in the above test.

Figure 2004278781
Figure 2004278781

表2に示す試験条件は、急加減速を行なうことにより、再現性よく水素脆性剥離を発生させることができる。この試験条件下で試験した試験結果を表3に示す。   Under the test conditions shown in Table 2, hydrogen embrittlement peeling can be generated with good reproducibility by performing rapid acceleration and deceleration. Table 3 shows the test results under the test conditions.

Figure 2004278781
Figure 2004278781

図4(a),(b)に比較例1において発生した水素脆性剥離を含む断面を示す。図4(a)は破面写真であり、図4(b)はその模式図である。上記の試験条件において水素脆性剥離を誘起させていることが分る。   FIGS. 4A and 4B show cross sections including hydrogen embrittlement peeling generated in Comparative Example 1. FIG. FIG. 4A is a photograph of the fracture surface, and FIG. 4B is a schematic view thereof. It can be seen that hydrogen embrittlement separation was induced under the above test conditions.

表3の試験結果によれば、従来品の比較例に比べ、本発明例のものは、いずれも長寿命を示すことが分る。とくに、本発明例2では、耐水素脆性剥離性が向上する比較例2の黒染処理材、および比較例3の13%Cr鋼の黒染処理材の両方よりも、さらに長寿命になることが分る。   According to the test results in Table 3, it can be seen that all of the examples of the present invention exhibit longer life than the comparative examples of the conventional products. In particular, in Example 2 of the present invention, the life becomes longer than both the blackening material of Comparative Example 2 and the 13% Cr steel blackening material of Comparative Example 3 in which the resistance to hydrogen embrittlement is improved. I understand.

本発明例3が特に長寿命となった原因を調査するために、本発明例1〜2、および、従来品の比較例1〜2の鋼材における表層部の球状化炭化物の面積率、およびオーステナイト結晶粒界のJIS規格での粒度番号を測定した。その結果を表4に示す。   In order to investigate the cause of the particularly long life of Invention Example 3, the area ratio of the spheroidized carbide in the surface layer portion of the steel materials of Invention Examples 1-2 and Comparative Examples 1-2 of the conventional product, and austenite The grain size number of the crystal grain boundary according to JIS standard was measured. Table 4 shows the results.

Figure 2004278781
Figure 2004278781

本発明例1の球状化炭化物の面積率が比較例1より大きく、JIS結晶粒度は比較例と比べて大きな相違はない。また、本発明例2では、球状化炭化物の面積率が比較例より大きく、またJIS結晶粒度は比較例より微細化されている。   The area ratio of the spheroidized carbide of Inventive Example 1 is larger than that of Comparative Example 1, and the JIS grain size is not significantly different from that of Comparative Example. Further, in Example 2 of the present invention, the area ratio of the spheroidized carbide was larger than that of the comparative example, and the JIS grain size was finer than that of the comparative example.

比較例1に比べて比較例2は長寿命であり、また、本発明例1は比較例2より、また、本発明例2は本発明例1より更に長寿命化されていることから、次の3つの要因が耐水素脆性剥離の抑制に効果があることが分る。
(1)窒素富化層を有すること。
(2)球状化炭化物の面積率が10%以上であること。
(3)オーステナイト結晶粒界がJIS規格の粒度番号で10番を超えること。
Compared with Comparative Example 1, Comparative Example 2 has a longer life, and Example 1 of the present invention has a longer life than Comparative Example 2, and Example 2 of the present invention has a longer life than Example 1 of the present invention. It can be seen that these three factors are effective in suppressing the hydrogen embrittlement resistance peeling.
(1) Having a nitrogen-enriched layer.
(2) The area ratio of the spheroidized carbide is 10% or more.
(3) The austenite crystal grain boundary exceeds JIS standard grain size number 10.

本発明例2は、上記3つの要因をすべて兼ね備えたために非常に長寿命を示したものである。上記の項目(1)のみでも耐水素脆性剥離の効果は認められるが、その延命効果は小さいため、少なくとも、本発明例1のように、(1)および(2)の2つの要件をともに備えることにより水素環境下で、水素脆性剥離割れを生じにくいころがり軸受を形成することができる。   The present invention example 2 has a very long life because it has all the above three factors. Although the effect of hydrogen embrittlement resistance peeling is recognized only with the above item (1), the effect of extending the life of the hydrogen embrittlement is small, and therefore at least the two requirements (1) and (2) are satisfied as in Example 1 of the present invention. This makes it possible to form a rolling bearing in which hydrogen embrittlement cracking is unlikely to occur in a hydrogen environment.

上記において、本発明の実施の形態について説明を行ったが、上記に開示された本発明の実施の形態は、あくまで例示であって、本発明の範囲はこれら発明の実施の形態に限定されない。本発明の範囲は、特許請求の範囲の記載によって示され、さらに特許請求の範囲の記載と均等の意味および範囲内でのすべての変更を含むものである。   Although the embodiments of the present invention have been described above, the embodiments of the present invention disclosed above are merely examples, and the scope of the present invention is not limited to these embodiments. The scope of the present invention is shown by the description of the claims, and further includes all modifications within the meaning and scope equivalent to the description of the claims.

本発明のころがり軸受およびその製造方法を用いることにより、水素が発生し、水素脆性剥離を生じやすい使用態様で使用されても、水素脆性剥離を抑制できるころがり軸受を提供できるので、この分野の部品に広範に利用されることが期待される。   By using the rolling bearing and the manufacturing method of the present invention, hydrogen is generated, and even when used in a usage mode in which hydrogen embrittlement is likely to occur, a rolling bearing capable of suppressing hydrogen embrittlement can be provided. It is expected to be used widely.

本発明の実施の形態におけるオルタネータ用軸受を示す図である。It is a figure showing a bearing for alternators in an embodiment of the invention. 本発明の実施例における各本発明例の処理を示す図であり、(a)は本発明例1の処理、(b)は本発明例2の処理、(c)は比較例1の処理、を示す図である。It is a figure showing processing of each example of the present invention in an example of the present invention, (a) processing of example 1 of the present invention, (b) processing of example 2 of the present invention, (c) processing of comparative example 1, FIG. 水素脆性剥離を再現する試験装置を示す図である。It is a figure showing a test device which reproduces hydrogen embrittlement exfoliation. 水素脆性剥離を示す図であり、(a)は断面の写真であり、(b)はその模式図である。It is a figure which shows hydrogen embrittlement peeling, (a) is a photograph of a cross section, (b) is the schematic diagram.

符号の説明Explanation of reference numerals

1 オルタネータ用軸受、2 転動体(鋼球)、3 外輪(軌道輪)、4 内輪(軌道輪)、5 プーリ、6 伝動ベルト用溝、7 保持器、10 オルタネータ、11 シャフト、15 破面、16 転走面、17 白層。   1 Alternator bearing, 2 rolling element (steel ball), 3 outer ring (track ring), 4 inner ring (track ring), 5 pulley, 6 groove for power transmission belt, 7 cage, 10 alternator, 11 shaft, 15 broken surface, 16 rolling surface, 17 white layer.

Claims (6)

ころがり軸受の、転動体、内輪および外輪のうちの少なくとも1つの部材が窒素富化層を有し、前記窒素富化層を有する部材の表層部における球状化炭化物の面積率が10%以上である、ころがり軸受。   At least one member of the rolling element, the inner ring, and the outer ring of the rolling bearing has a nitrogen-enriched layer, and an area ratio of spheroidized carbide in a surface layer portion of the member having the nitrogen-enriched layer is 10% or more. , Rolling bearings. 前記窒素富化層を有する部材のオーステナイト結晶粒の粒度番号が10番をこえる、請求項1に記載のころがり軸受。   2. The rolling bearing according to claim 1, wherein the member having the nitrogen-enriched layer has an austenite crystal grain having a grain size number of more than 10. 前記窒素富化層を有する部材は、1.3〜1.6のCP(Carbon Potential)値で浸炭窒化処理された後、その温度から油冷されている、請求項1または2に記載のころがり軸受。   The rolling according to claim 1, wherein the member having the nitrogen-enriched layer is subjected to carbonitriding at a CP (Carbon Potential) value of 1.3 to 1.6, and then oil-cooled from the temperature. bearing. 前記窒素富化層を有する部材は、その鋼材本体のA1点以上で浸炭窒化処理された後、A1点より低い温度に冷却され、次いでその鋼材本体のA1点以上であって、前記浸炭窒化処理温度より低い焼入れ温度域に再加熱され、焼入れされている、請求項1または2に記載のころがり軸受。   The member having the nitrogen-enriched layer is subjected to carbonitriding at a point A1 or higher of the steel main body, and then cooled to a temperature lower than the point A1. The rolling bearing according to claim 1, wherein the rolling bearing is reheated and quenched to a quenching temperature range lower than the temperature. 転動体、内輪および外輪を含むころがり軸受の製造方法であって、
前記転動体、内輪および外輪のうちの少なくとも1つの部材を形成する鋼材を、A1点以上の温度に加熱して1.3〜1.6のCP(Carbon Potential)値で浸炭窒化処理した後、A1点より低い温度に油冷する、ころがり軸受の製造方法。
A method of manufacturing a rolling bearing including a rolling element, an inner ring and an outer ring,
The rolling element, a steel material forming at least one member of the inner ring and the outer ring, after heating to a temperature of the A1 point or more and carbonitriding at a CP (Carbon Potential) value of 1.3 to 1.6, A method for manufacturing a rolling bearing, wherein oil is cooled to a temperature lower than the point A1.
転動体、内輪および外輪を含むころがり軸受の製造方法であって、
前記転動体、内輪および外輪のうちの少なくとも1つの部材を形成する鋼材を、A1点以上の温度に加熱して浸炭窒化処理した後、A1点より低い温度に冷却し、次いでA1点以上の温度であって、前記浸炭窒化処理の温度より低い焼入れ温度域に再加熱し、焼入れする、ころがり軸受の製造方法。
A method of manufacturing a rolling bearing including a rolling element, an inner ring and an outer ring,
The steel material forming at least one member of the rolling element, the inner race and the outer race is subjected to carbonitriding by heating to a temperature of A1 point or higher, then cooled to a temperature lower than A1 point, and then cooled to a temperature of A1 point or higher. A method for producing a rolling bearing, comprising reheating and quenching to a quenching temperature range lower than the temperature of the carbonitriding treatment.
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Cited By (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JP2006144889A (en) * 2004-11-18 2006-06-08 Ntn Corp Rotation support mechanism of planetary gear mechanism
WO2007125767A1 (en) * 2006-04-28 2007-11-08 Ntn Corporation Carbonitriding process, process for production of macine parts, and machine parts
JP2012149757A (en) * 2011-01-21 2012-08-09 Ntn Corp Bearing ring and rolling bearing
US9487843B2 (en) 2011-01-21 2016-11-08 Ntn Corporation Method for producing a bearing ring

Cited By (7)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JP2006144889A (en) * 2004-11-18 2006-06-08 Ntn Corp Rotation support mechanism of planetary gear mechanism
JP4694180B2 (en) * 2004-11-18 2011-06-08 Ntn株式会社 Rolling support mechanism for planetary gear mechanism
WO2007125767A1 (en) * 2006-04-28 2007-11-08 Ntn Corporation Carbonitriding process, process for production of macine parts, and machine parts
JP2007297663A (en) * 2006-04-28 2007-11-15 Ntn Corp Carbo-nitriding process, method for manufacturing machine part, and machine part
US8128761B2 (en) 2006-04-28 2012-03-06 Ntn Corporation Carbonitriding method, machinery component fabrication method, and machinery component
JP2012149757A (en) * 2011-01-21 2012-08-09 Ntn Corp Bearing ring and rolling bearing
US9487843B2 (en) 2011-01-21 2016-11-08 Ntn Corporation Method for producing a bearing ring

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