JP2011184742A - Steel for machine structure suitable for friction pressure welding, and friction pressure-welded component - Google Patents

Steel for machine structure suitable for friction pressure welding, and friction pressure-welded component Download PDF

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JP2011184742A
JP2011184742A JP2010051825A JP2010051825A JP2011184742A JP 2011184742 A JP2011184742 A JP 2011184742A JP 2010051825 A JP2010051825 A JP 2010051825A JP 2010051825 A JP2010051825 A JP 2010051825A JP 2011184742 A JP2011184742 A JP 2011184742A
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JP5607956B2 (en
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Tomokazu Masuda
智一 増田
Akihiro Matsugaseko
亮廣 松ヶ迫
Mutsuhisa Nagahama
睦久 永濱
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Kobe Steel Ltd
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Abstract

<P>PROBLEM TO BE SOLVED: To provide a low carbon steel for a machine structure which is suitable for friction pressure welding, in which component properties such as fatigue strength and impact strength are improved together with cold workability such as cold forging and machinability, and a friction pressure-welded component. <P>SOLUTION: N in the steel of a stock slow carbon steel member is beforehand made to exist as a compound N; further, abundance as solid solution N is regulated, and MnS with a fixed size and elongated shape is increased; thus its cold workability and machinability are improved, and simultaneously, the compound N in the steel in a heat affected zone in the low carbon steel member is decomposed by frictional heat upon friction pressure welding to increase the amount of the solid solution N; thus ferrite or austenite (cementite) in the heat affected zone is solid solution-strengthened by dynamic strain aging owing to the solid solution N; further, MnS is finely parted, and its joining strength after the friction pressure welding is improved. <P>COPYRIGHT: (C)2011,JPO&INPIT

Description

本発明は、摩擦圧接される用途に適した機械構造用の鋼材および機械構造用の鋼材が他の鋼材と摩擦圧接されて複合鋼とされた摩擦圧接部品に関する。   The present invention relates to a steel material for machine structure suitable for applications subjected to friction welding and a friction welding component in which a steel material for machine structure is friction welded to another steel material to form a composite steel.

例えば、自動車のエンジン、変速機、差動機などに用いられる減速ギア、デフギアなどの歯車、CVTプーリーなどの鋼製の機械構造部品は、多くの場合、表層部の硬さを高める必要があり、素材である機械構造用鋼材に、浸炭、窒化、浸炭窒化などの表面硬化処理を施す。また、これらの機械構造部品は、同時に、最終部品の形状精度を保証するために、精密な切削加工を要する部品でもある。   For example, steel mechanical structural parts such as gears such as reduction gears, differential gears, and CVT pulleys used in automobile engines, transmissions, differentials, etc., often need to increase the hardness of the surface layer, Surface hardening treatment such as carburizing, nitriding, and carbonitriding is performed on the structural steel material. These mechanical structural parts are also parts that require precise cutting in order to guarantee the shape accuracy of the final part.

自動車などの車両に用いられるこれら機械構造部品は、近年、省エネルギー化による車体重量の軽量化に伴い、小型化が追求されている。そして、自動車などのエンジンの高出力化に伴い、前記小型化との相乗作用で、これら機械構造部品への負荷は増大しつつある。このため、これらの機械構造部品には、基本的な要求特性である強度、靭性に加えて、衝撃特性、曲げ疲労特性、面圧疲労特性といった各種特性の向上がより求められている。   In recent years, these mechanical structural parts used for vehicles such as automobiles have been pursued to be miniaturized as the weight of the vehicle body is reduced by energy saving. And with the increase in the output of engines such as automobiles, the load on these mechanical structural parts is increasing due to the synergistic effect with the downsizing. For this reason, these mechanical structural parts are required to improve various characteristics such as impact characteristics, bending fatigue characteristics, and surface fatigue characteristics, in addition to basic required characteristics such as strength and toughness.

通常、これら機械構造部品の素材である鋼材には、加工性に優れた低炭素鋼材(肌焼き鋼、フェライトとパーライトとの混合組織)が用いられる。この低炭素鋼材は、通常、熱間圧延や熱間鍛造による棒材や線材などへの加工後に、必要により、冷間鍛造などの冷間加工が施された上で、機械構造部品形状に精密な切削・仕上げ加工が行われている。   Usually, a low carbon steel material (case-hardened steel, mixed structure of ferrite and pearlite) excellent in workability is used as the steel material as the material of these mechanical structural parts. This low-carbon steel is usually precision processed into machine structural parts after cold working such as cold forging, if necessary, after processing into bars and wires by hot rolling or hot forging. Cutting and finishing are performed.

ここで、上記のように負荷増大に対応した機械構造部品の素材として、素材である機械構造用鋼材の強度、靭性を高くすると、前記冷間鍛造などの冷間加工や精密な切削加工が著しく困難となる。したがって、前記高強度、高靭性な部品特性と冷間加工性や被削性とを兼備した鋼材が求められるが、強度と冷間加工性や被削性とは相反する関係にあり、単一の機械構造用鋼材で、強度と冷間加工性や被削性とを両立させることは著しく困難である。   Here, if the strength and toughness of the mechanical structural steel material, which is the raw material of the machine structural component corresponding to the load increase as described above, is increased, cold working such as cold forging and precise cutting work are remarkably performed. It becomes difficult. Therefore, there is a demand for a steel material that combines the above-mentioned high strength and high toughness component characteristics with cold workability and machinability. However, there is a conflict between strength and cold workability and machinability. It is extremely difficult to achieve both strength, cold workability, and machinability with steel materials for machine structural use.

このため、前記高強度、高靭性な部品特性と冷間加工性や被削性とを両立させる方策の一つとして、強度、靭性などの前記部品特性が必要な部分に用いる鋼材と、冷間加工性や被削性が必要な部分に用いる鋼材とをそれぞれ別個に準備し、これら特性が各々異なる両鋼材を互いに接合することによって、複合鋼材あるいは複合鋼部品とし、前記部品特性と被削性を両方達成する方法がある。   For this reason, as one of the measures to achieve both the high strength and high toughness of the component characteristics and the cold workability and machinability, the steel material used for the parts that require the component characteristics such as strength and toughness, Steel materials used for parts that require workability and machinability are prepared separately, and both steel materials having different characteristics are joined together to form a composite steel material or a composite steel part. There are ways to achieve both.

このような複合鋼材を作成するための、互いの鋼材間あるいは鋼部材間の接合方法としては、大きく分けて溶融接合法と固相接合法に分類される。このうち溶融接合では、互いの鋼材の接合部分が融点以上の高温状態となるため、接合部位で結晶粒の粗大化、気泡の発生など接合欠陥が発生しやすい。また、熱影響部が大きくなり、母材と熱影響部の界面で割れが発生しやすい問題も生じる。   Methods for joining such steel materials or steel members for producing such a composite steel material are roughly classified into a melt joining method and a solid phase joining method. Among these, in the fusion bonding, since the joining portions of the steel materials are in a high temperature state higher than the melting point, joining defects such as coarsening of crystal grains and generation of bubbles are likely to occur at the joining portions. In addition, the heat affected zone becomes large, and there is a problem that cracks are likely to occur at the interface between the base material and the heat affected zone.

一方、固相接合は、互いの鋼材の接合面が固相面同士の溶接方法のことであり、溶加材を用いることなく、母材の融点以下の温度で接合することができる。代表的な固相接合法としては摩擦圧接法がある。この摩擦圧接法は、2つの鋼材同士(鋼部材同士)を加圧・回転させながら、接触面(当接面)に摩擦熱を発生させることで、互いの鋼材の接合部分(以下、接合部とも言う)を加熱、軟化した後、この接合部に対するアップセット力(圧接力)を作用させて接合(溶着)する方法である。   On the other hand, solid phase bonding is a welding method in which the joining surfaces of the steel materials are solid phase surfaces, and can be joined at a temperature below the melting point of the base material without using a filler material. As a typical solid phase bonding method, there is a friction welding method. This friction welding method generates frictional heat on the contact surface (contact surface) while pressurizing and rotating two steel materials (steel members) to each other, thereby joining each steel material (hereinafter referred to as a joint part). This is a method of joining (welding) by heating and softening, and then applying an upset force (pressure contact force) to the joint.

このような摩擦圧接法では、半溶融状態に加熱された部分がアップセット力の作用でバリとして接合面から排出されるため、清浄面同士が融点以下の温度で接合されることになる。このため、前記溶融接合法と比較して、接合部位で結晶粒の粗大化、気泡の発生、熱影響部の界面による割れなどが発生しにくい特徴がある。   In such a friction welding method, a portion heated to a semi-molten state is discharged from the joining surface as a burr by the action of the upset force, and the clean surfaces are joined at a temperature below the melting point. For this reason, compared with the said melt-bonding method, it has the characteristics that the coarsening of a crystal grain, the generation | occurrence | production of a bubble, the crack by the interface of a heat affected zone, etc. do not generate | occur | produce easily in a joining part.

このような鋼材同士の摩擦圧接方法自体は従来から公知であって、例えば、特許文献1などで、この摩擦圧接方法の改良技術が提案されている。即ち、特許文献1では、摩擦圧接方法における、投入エネルギーおよび素材の無駄遣いを抑え、製品の寸法精度、接合強度、機械的性質のばらつきを抑えることが可能であることが開示されている。ただし、この特許文献1には、摩擦圧接方法に適した、素材鋼材に関する具体的な記述はない。   Such a friction welding method itself between steel materials is conventionally known. For example, Patent Document 1 discloses an improved technique for the friction welding method. That is, Patent Document 1 discloses that it is possible to suppress waste of input energy and materials in the friction welding method, and to suppress variations in product dimensional accuracy, bonding strength, and mechanical properties. However, in this patent document 1, there is no specific description regarding the material steel material suitable for the friction welding method.

一方、このような特徴を有する摩擦圧接法を鋼材同士の接合に適用した場合には、前記溶融接合法ほどではないにせよ、やはり、摩擦熱により熱影響を受ける部分(HAZ部)の強度低下や、逆に接合部分の強度増加が問題となる。この接合部分では、摩擦熱による加熱後、周りの母材によって急速に冷却されるため、マルテンサイト相となりやすく、強度が増加しやすいからである。そして、このような熱影響部の強度低下や接合部分の強度増加が大きいと、母材、前記熱影響部、前記接合部分の、摩擦圧接された複合鋼材(複合鋼部品)の部位による強度変動が大きく、疲労強度、衝撃強度などの部品特性を低下させることとなる。   On the other hand, when the friction welding method having such characteristics is applied to the joining of steel materials, the strength of the portion (HAZ portion) that is affected by the heat of friction is reduced, though not as much as the fusion welding method. On the contrary, an increase in the strength of the joined portion becomes a problem. This is because the joint portion is rapidly cooled by the surrounding base material after being heated by frictional heat, so that it tends to become a martensite phase and the strength tends to increase. If the strength reduction of the heat affected zone and the strength increase of the joined portion are large, the strength fluctuation due to the friction welded portion of the base material, the heat affected zone, and the joined portion of the composite steel material (composite steel part) Is large and deteriorates the component characteristics such as fatigue strength and impact strength.

このような課題に対して、前記熱影響部の強度低下だけ、あるいは前記接合部分の強度増加だけなど、個別の問題への対応でしかないが、従来から摩擦圧接用の素材鋼材側を改良した技術が種々提案されている。   For such a problem, only the strength reduction of the heat affected zone or only the strength increase of the joint portion can be dealt with individually, but the material steel side for friction welding has been improved conventionally. Various techniques have been proposed.

例えば、特許文献2には、前記熱影響部の強度低下を抑制した、摩擦圧接用の高強度電縫鋼管の製造方法が提案されている。この特許文献2では、C:0.08〜0.23%、Si:0.5 %以下、Mn:1.8 %以下、Nb:0.01〜0.1 %、Mo:0.05〜0.60%を含有する鋼を、熱間圧延後、摩擦圧接時に析出するMo、Nbの炭窒化物を固溶状態に保つため、熱延鋼板の巻取り温度を450 ℃未満とする。そして、これら固溶状態としたNb、Moを摩擦圧接の際に、炭窒化物として析出させ、析出強化によって熱影響部の軟化を抑制している。   For example, Patent Document 2 proposes a method for manufacturing a high-strength ERW steel pipe for friction welding, in which a decrease in strength of the heat-affected zone is suppressed. In Patent Document 2, a steel containing C: 0.08 to 0.23%, Si: 0.5% or less, Mn: 1.8% or less, Nb: 0.01 to 0.1%, Mo: 0.05 to 0.60% is subjected to friction after hot rolling. In order to keep the Mo and Nb carbonitrides precipitated during pressure welding in a solid solution state, the coiling temperature of the hot-rolled steel sheet is set to less than 450 ° C. These Nb and Mo in a solid solution state are precipitated as carbonitrides during friction welding, and the softening of the heat affected zone is suppressed by precipitation strengthening.

しかし、前記した析出強化は、単に熱影響部だけでなく、通常は互いの鋼材の接合部分にまで及ぶ。このような接合部分は、摩擦熱による加熱後、周りの母材によって急速に冷却されるため、マルテンサイト相となりやすく、元々強度が増加しやすい。そこへ、この析出強化も加わった場合、このような接合部分は、前記マルテンサイト相化との相乗効果によって、接合部分の強度は逆に顕著に増加してしまう。   However, the precipitation strengthening described above extends not only to the heat-affected zone but also to the joint portion of the steel materials. Since such a joint portion is rapidly cooled by the surrounding base material after being heated by frictional heat, it tends to become a martensite phase and tends to increase in strength originally. If this precipitation strengthening is also added, the strength of the joint portion of such a joint portion increases conversely due to a synergistic effect with the martensite phase.

このような接合部分の強度増加は、前記した衝撃、曲げ疲労、面圧疲労といった負荷が増大した機械構造部品では、使用中の接合部分の脆化を著しく促進させ、割れを発生しやすくする。このため、機械構造部品あるいは機械構造用鋼材としての信頼性を低下させる。   Such an increase in the strength of the joint portion significantly accelerates the embrittlement of the joint portion in use and makes it easy to generate cracks in mechanical structural parts with increased loads such as impact, bending fatigue, and surface fatigue. For this reason, the reliability as a machine structural component or steel for machine structures is reduced.

特許文献3には、このような摩擦圧接による接合部分の強度増加を、素材である高炭素熱延鋼材側で抑制する技術が開示されている。この特許文献3では、微量の固溶Nbを含有させることによって、摩擦圧接の高圧力下での急速加熱における、高炭素鋼材のオーステナイト結晶粒の粗大化を防止し、接合部分の硬さ増加と脆化を抑制している。この場合、固溶Nbは、摩擦圧接後に、NbC として析出して結晶粒の粗大化防止に寄与している。   Patent Document 3 discloses a technique for suppressing an increase in strength of a joint portion due to such friction welding on the high carbon hot rolled steel material side that is a material. In this Patent Document 3, by containing a small amount of solute Nb, coarsening of austenite crystal grains of a high carbon steel material in rapid heating under high pressure of friction welding is prevented, and the hardness of the joined portion is increased. Brittleness is suppressed. In this case, solute Nb precipitates as NbC after friction welding and contributes to prevention of crystal grain coarsening.

ただ、このような固溶Nbの利用は、摩擦接合のままで使用される鋼材あるいは鋼部品(焼戻し付与材)の場合には有効であるが、摩擦圧接後の鋼材あるいは鋼部品に浸炭処理などの表面硬化処理を施して、部品強度を更に向上させる場合には、意味が無くなる。即ち、このような表面硬化処理では、大抵鋼材あるいは鋼部品を高温に加熱するために、一旦析出したNbC がこの加熱によって再び分解し始める。このため、部分的な結晶粒の粗大化が発生しやすく、この表面硬化処理後の冷却によって、旧オーステナイト粒径のばらついたマルテンサイト相となる。このような結晶粒径のばらつきは、やはり疲労強度、衝撃強度などの部品特性を著しく低下させる。このため、前記した衝撃、曲げ疲労、面圧疲労といった負荷が増大した機械構造部品あるいは機械構造用鋼材としての信頼性を低下させる。   However, the use of such solute Nb is effective in the case of steel materials or steel parts (tempering imparting materials) that are used in the state of friction welding, but carburizing the steel materials or steel parts after friction welding. When the surface hardening treatment is applied to further improve the component strength, the meaning is lost. That is, in such a surface hardening treatment, in order to heat a steel material or a steel part to a high temperature, NbC once precipitated starts to decompose again by this heating. For this reason, partial coarsening of crystal grains is likely to occur, and cooling after the surface hardening treatment results in a martensitic phase with a variation in prior austenite grain size. Such variation in crystal grain size also significantly reduces component characteristics such as fatigue strength and impact strength. For this reason, the reliability as a machine structural component or a steel material for machine structure having increased loads such as impact, bending fatigue, and surface pressure fatigue is lowered.

因みに、この他の技術として、特許文献4では、Cが0.1%以上の中高炭素鋼材について、摩擦圧接による接合部分(接合界面)に生じる硬化層(酸化物)をバリとして排出して、接合部分の曲げ延性を確保するために、素材鋼の組織を制御している。即ち、素材鋼の組織をフェライトとパーライトとを合わせた面積率を40%未満とした、ベイナイト組織またはベイナイトとマルテンサイトとの混合組織として、摩擦圧接時の加熱による軟化を遅らせて、前記硬化層をバリとして排出しやすくし、接合部分の曲げ延性を確保している。   By the way, as another technique, in Patent Document 4, C is 0.1% or more of medium and high carbon steel materials, and the hardened layer (oxide) generated at the joining portion (joining interface) by friction welding is discharged as burrs. In order to ensure the bending ductility of the joint portion, the structure of the material steel is controlled. That is, the hardened layer is made of a bainite structure or a mixed structure of bainite and martensite in which the area ratio of the material steel is less than 40% by combining ferrite and pearlite, and softening due to heating during friction welding is delayed. Is easily discharged as burrs, and the bending ductility of the joint is ensured.

また、特許文献5では、Cが0.1%以上の中高炭素鋼材について、摩擦圧接した複合鋼材接合部の表面を、超音波振動端子により打撃して、接合部の応力集中を緩和して、耐疲労強度を向上させている。   Moreover, in patent document 5, about the medium and high carbon steel materials with C 0.1% or more, the surface of the composite steel material joint part friction-welded is hit | damaged by an ultrasonic vibration terminal, the stress concentration of a junction part is relieve | moderated, Fatigue strength is improved.

ただ、これら特許文献4、5は、いずれも中高炭素鋼材(ベイナイト組織またはベイナイトとマルテンサイトとの混合組織)を対象としており、通常の機械構造部品の素材である低炭素鋼材(フェライトとパーライトとの混合組織)の疲労強度、衝撃強度の向上には適用できない。   However, these Patent Documents 4 and 5 are all intended for medium and high carbon steel materials (bainite structure or a mixed structure of bainite and martensite), and are low carbon steel materials (ferrite and pearlite) that are materials of ordinary mechanical structural parts. It cannot be applied to the improvement of fatigue strength and impact strength of the mixed structure.

特開平11−47958号公報Japanese Patent Laid-Open No. 11-47958 特開平4−116123号公報JP-A-4-116123 特開2002−294404号公報JP 2002-294404 A 特開2003−183768号公報JP 2003-183768 A 特開2006−297398号公報JP 2006-297398 A

前記特許文献2、3の、素材側鋼材のNb、Moなどを予め固溶させておいて、摩擦圧接の際の析出強化によって熱影響部の軟化を抑制する、従来の冶金的な手法には限界がある。したがって、低炭素鋼材には、これに代わる冶金的な手法を用いて、摩擦圧接による熱影響部の過度の強度低下や接合部分の過度の強度増加を抑制して摩擦圧接後の接合強度を向上させる手段が求められている。   In the conventional metallurgical methods in which Nb and Mo of the material side steel materials of Patent Documents 2 and 3 are previously dissolved, and the softening of the heat affected zone is suppressed by precipitation strengthening at the time of friction welding. There is a limit. Therefore, for low-carbon steel materials, an alternative metallurgical method is used to improve the joint strength after friction welding by suppressing an excessive decrease in strength of the heat-affected zone and an excessive increase in strength at the joint due to friction welding. There is a need for a means to do this.

また、低炭素鋼材には、摩擦圧接法によって複合鋼化(複合鋼部品)されるにしても、前記自動車などのエンジン部品用などの摩擦圧接部品として、前記した小型化、高出力化に伴う部品への、冷間鍛造などの冷間加工性や被削性の更なる向上も求められている。   Moreover, even if low carbon steel is made into composite steel (composite steel parts) by the friction welding method, it is accompanied by the above-mentioned miniaturization and high output as friction welding parts for engine parts such as automobiles. There is also a demand for further improvements in cold workability and machinability of parts such as cold forging.

ただ、これら摩擦圧接後の接合強度の向上と、冷間加工性や被削性の向上とは、低炭素鋼材にとって、互いに相矛盾する難しい技術課題となる。したがって、このような摩擦圧接用の低炭素鋼材の、冷間加工性や被削性の向上とともに、摩擦圧接後の接合強度を向上させるような冶金的な手法は、これまであまり提案されていない。   However, the improvement of the joint strength after friction welding and the improvement of cold workability and machinability are difficult technical issues that contradict each other for low carbon steel materials. Therefore, metallurgical methods that improve the cold workability and machinability of such low carbon steel materials for friction welding as well as the joint strength after friction welding have not been proposed so far. .

本発明はかかる問題に鑑みなされたもので、冷間加工性や被削性の向上とともに、疲労強度、衝撃強度などの部品特性を向上させた、摩擦圧接に適した機械構造用の低炭素鋼材および衝撃特性、曲げ疲労特性に優れた摩擦圧接部品を提供することを目的とする。   The present invention has been made in view of such problems, and has improved cold workability and machinability, and improved part characteristics such as fatigue strength and impact strength, and is a low carbon steel material for machine structures suitable for friction welding. Another object of the present invention is to provide a friction welded part having excellent impact characteristics and bending fatigue characteristics.

上記目的を達成するための、本発明の摩擦圧接に適した機械構造用鋼材の要旨は、質量%で、C:0.08〜0.61%、Si:0.08〜0.5%、Mn:0.4〜1.5%、P:0.03%以下(但し0%を含まない)、S:0.005〜0.1%、Cr:0.4〜2%、Al:0.005〜0.1%、N:0.02%以下(但し0%を含まない)を各々含み、残部Feおよび不可避的不純物からなるとともに、鋼中の化合物Nの含有量が0.006〜0.02%で、且つ、固溶N量が0.0015%以下(但し0%を含む)であり、最大長さが2μm以上のMnSが鋼中に1mm2 当たり100〜4000個存在し、これらMnSの平均アスペクト比が2以上であることとする。 In order to achieve the above object, the gist of the steel for machine structure suitable for friction welding according to the present invention is mass%, C: 0.08 to 0.61%, Si: 0.08 to 0.5%, Mn: 0.4 to 1.5%, P: 0.03% or less (excluding 0%), S: 0.005 to 0.1%, Cr: 0.4 to 2%, Al: 0 0.005 to 0.1%, N: not more than 0.02% (but not including 0%), each of which consists of the balance Fe and unavoidable impurities, and the content of compound N in the steel is 0.006 to 0.02% and the amount of solute N is 0.0015% or less (including 0%), and MnS having a maximum length of 2 μm or more is present in steel in an amount of 100 to 4000 per mm 2 , The average aspect ratio of these MnS shall be 2 or more.

また、上記目的を達成するための、本発明の曲げ疲労特性に優れた摩擦圧接部品の要旨は、質量%で、C:0.08〜0.61%、Si:0.08〜0.5%、Mn:0.4〜1.5%、P:0.03%以下(但し0%を含まない)、S:0.005〜0.1%、Cr:0.4〜2%、Al:0.005〜0.1%、N:0.02%以下(但し0%を含まない)を各々含み、残部Feおよび不可避的不純物からなるとともに、鋼中の化合物Nの含有量が0.006〜0.02%で、且つ、固溶N量が0.0015%以下(但し0%を含む)であり、最大長さが2μm以上のMnSが鋼中に1mm2 当たり100〜4000個存在し、これらMnSの平均アスペクト比が2以上である機械構造用鋼材と、他の炭素鋼材あるいは合金鋼材とが、摩擦圧接によって接合されて所望の形状の複合鋼とされ、更に、表面硬化処理および焼戻し処理が施されてなる摩擦圧接部品であって、前記摩擦圧接によって形成された接合部から1mm幅の範囲の前記機械構造用鋼材側の熱影響部の鋼中における、アスペクト比が2以下で、且つ、最大長さが1μm以下のMnSを、1mm2 当たり25個以下(但し0個を含む)に規制したことである。 In order to achieve the above object, the gist of the friction welded part excellent in bending fatigue characteristics of the present invention is mass%, C: 0.08 to 0.61%, Si: 0.08 to 0.5. %, Mn: 0.4 to 1.5%, P: 0.03% or less (excluding 0%), S: 0.005 to 0.1%, Cr: 0.4 to 2%, Al : 0.005 to 0.1%, N: 0.02% or less (excluding 0%), respectively, and the balance is composed of Fe and unavoidable impurities, and the content of compound N in the steel is 0.00. in 006-0.02%, and a dissolved amount of N is 0.0015% or less (except including 0%), the maximum length is more than 2 [mu] m MnS is present 100 to 4000 per 1 mm 2 in the steel However, the mechanical structural steel having an average aspect ratio of MnS of 2 or more and other carbon steel or alloy steel are in friction. A friction welded part that is joined by pressure welding to form a composite steel of a desired shape, and further subjected to surface hardening treatment and tempering treatment, wherein the joint in the range of 1 mm width from the joint formed by the friction welding Restricting MnS with an aspect ratio of 2 or less and a maximum length of 1 μm or less to 25 or less (including 0) per mm 2 in the steel in the heat-affected zone on the machine structural steel side It is.

ここで、前記化合物N(化合物窒素)とは、鋼中の全N(全窒素)のうち、鋼マトリックスに固溶した固溶Nを除き、窒化物や炭窒化物などの、他の元素との化合物として(化合物を形成して)鋼中に存在するN(窒素)の総称である。   Here, the compound N (compound nitrogen) refers to other elements such as nitride and carbonitride except for the solid solution N dissolved in the steel matrix among all N (total nitrogen) in the steel. Is a generic name for N (nitrogen) present in steel as a compound of (form a compound).

本発明者は、素材側低炭素鋼材の合金元素の予めの固溶と摩擦圧接の際の析出強化との関係(冶金的手法)について改めて検討した。この結果、摩擦圧接の前後で鋼中のNの存在形態を変化させることが、摩擦圧接後の接合強度の向上と、冷間加工性や被削性の向上という、低炭素鋼材にとって相矛盾する技術課題解決に有効であることを知見した。   This inventor examined again the relationship (metallurgical method) with the solid solution of the alloy element of the raw material side low carbon steel materials, and the precipitation strengthening in the friction welding. As a result, changing the form of N in the steel before and after friction welding contradicts the low carbon steel materials, namely, improvement in joint strength after friction welding and improvement in cold workability and machinability. It was found that it is effective for solving technical problems.

また、摩擦圧接の前後で、このようにNの存在形態を変化させることによって、摩擦圧接の前後で、鋼中に存在するMnSの形状も変化させることができ、前記N制御との相乗効果で、摩擦圧接後の接合強度の向上と、冷間加工性や被削性の向上との相矛盾する技術課題解決に更に有効であることを知見した。   In addition, by changing the existence form of N before and after the friction welding, the shape of MnS existing in the steel can be changed before and after the friction welding, which is a synergistic effect with the N control. The present inventors have found that it is further effective in solving technical problems that contradict the improvement of joint strength after friction welding and the improvement of cold workability and machinability.

すなわち、摩擦圧接の前に、素材低炭素鋼材の鋼中のNを、化合物Nとして存在させるとともに、固溶Nとしての存在量を規制する。これによって、素材としての低炭素鋼材や摩擦圧接されて複合鋼としての低炭素鋼材の、冷間加工性や被削性を向上させる。同時に、素材低炭素鋼材にSを添加して(Sの含有量を増して)、鋼中に一定のサイズの伸長した形状のMnSを増加させることによって、被削性をより向上させる。   That is, before friction welding, N in the steel of the raw material low-carbon steel is allowed to exist as the compound N, and the abundance as the solute N is regulated. This improves the cold workability and machinability of the low carbon steel material as a raw material and the low carbon steel material as a composite steel by friction welding. At the same time, by adding S to the raw material low-carbon steel (increasing the S content), the machinability is further improved by increasing MnS having a certain size of elongated shape in the steel.

素材低炭素鋼材の組成や組織をこのように予め準備することによって、摩擦圧接の際の摩擦熱とひずみによって、摩擦圧接後の低炭素鋼材における熱影響部の、鋼中の化合物Nを分解させ、固溶N量を増量させる。そして、この固溶Nによる動的ひずみ時効によって、前記熱影響部のフェライトあるいはオーステナイト(セメンタイト)を強化し、前記熱影響部の過度の強度低下や、接合部分の過度の強度増加を抑制して、摩擦圧接後の接合強度を向上させる。   By preparing the composition and structure of the raw material low-carbon steel in this way, the compound N in the steel of the heat-affected zone in the low-carbon steel after friction welding is decomposed by friction heat and strain during friction welding. Increase the amount of solute N. And by dynamic strain aging by this solid solution N, the ferrite or austenite (cementite) of the heat affected zone is strengthened, and an excessive decrease in strength of the heat affected zone and an excessive increase in strength of the bonded portion are suppressed. , Improve the bonding strength after friction welding.

同時に、前記固溶Nによる動的ひずみ時効に伴う、MnS周囲のフェライトあるいはオーステナイト(セメンタイト)の前記強化によって、摩擦圧接による強ひずみ加工とも相まって、予め存在する一定のサイズの伸長した形状のMnSを細かく分断して微細化させる。そして、このように微細化(分断、分解)されたMnSが、前記熱影響部のオーステナイト粒径の整粒化に寄与するようにして、摩擦圧接後の接合強度を向上させる。また、このようなMnSの微細化は、前記一定のサイズの伸長した形状のMnSの前記熱影響部の強度劣化への影響(寄与)をなくす効果もあり、やはり摩擦圧接後の接合強度を向上させる。   At the same time, due to the strengthening of ferrite or austenite (cementite) around MnS accompanying the dynamic strain aging due to the solid solution N, combined with the high strain processing by friction welding, the preexisting elongated size of MnS is obtained. Finely divide into fine pieces. And MnS refined | miniaturized (partitioning and decomposition | disassembly) in this way contributes to the granulation of the austenite particle size of the said heat affected zone, and improves the joint strength after friction welding. In addition, such miniaturization of MnS also has the effect of eliminating the influence (contribution) to the strength degradation of the heat-affected zone of the elongated shape of MnS, which also improves the joint strength after friction welding. Let

本発明によれば、機械構造用の低炭素鋼材(肌焼き鋼)につき、摩擦圧接の際の摩擦熱により熱影響を受ける部分(HAZ部)の強度低下や、互いの鋼材の接合部分の強度増加を、各々抑制できる。しかも、これらの効果は、続く浸炭、窒化、浸炭窒化などの表面硬化処理を施しても損なわれることがない。したがって、摩擦圧接による強度ばらつきを抑制した複合鋼部材とでき、更に、表面硬化処理や、その後の焼戻し熱処理を施すことによって、摩擦接合部品の欠点であった疲労強度、衝撃強度などの特性の低下を抑制した鋼部品とすることができる。また、面疲労特性、曲げ疲労特性、被削性が要求される部位に関しても、それぞれ特性を満足させることができる。   According to the present invention, with respect to low carbon steel material (case-hardened steel) for mechanical structure, the strength of the part (HAZ part) affected by frictional heat at the time of friction welding is reduced, and the strength of the joint part of each steel material Each increase can be suppressed. Moreover, these effects are not impaired even if a subsequent surface hardening treatment such as carburizing, nitriding, carbonitriding, or the like is performed. Therefore, it can be a composite steel member that suppresses variation in strength due to friction welding, and furthermore, by performing surface hardening treatment and subsequent tempering heat treatment, characteristics such as fatigue strength and impact strength, which were disadvantages of friction bonded parts, are reduced. It can be set as the steel part which suppressed. In addition, the characteristics can be satisfied with respect to the parts requiring surface fatigue characteristics, bending fatigue characteristics, and machinability.

鋼材の組成:
まず、本発明鋼材の化学成分組成の限定理由について説明する。本発明機械構造用の低炭素鋼材(肌焼き鋼)の化学成分組成は、前記した自動車のエンジン部品などの機械構造部品に要求される強度や靭性特性、これに加えた衝撃特性、曲げ疲労特性、面圧疲労特性などの特性向上のためや、これらの特性向上のための前記本発明組織とするための前提条件となる。
Steel composition:
First, the reason for limiting the chemical composition of the steel of the present invention will be described. The chemical component composition of the low carbon steel material (case-hardened steel) for the machine structure of the present invention is the strength and toughness characteristics required for machine structural parts such as the engine parts of automobiles described above, impact characteristics in addition to these, and bending fatigue characteristics. Therefore, it is a precondition for improving the characteristics such as surface fatigue characteristics and for obtaining the structure of the present invention for improving these characteristics.

このため、本発明鋼材は、質量%で、C:0.08〜0.61%、Si:0.08〜0.5%、Mn:0.4〜1.5%、P:0.03%以下(但し0%を含まない)、S:0.005〜0.1%、Cr:0.4〜2%、Al:0.005〜0.1%、N:0.02%以下(但し0%を含まない)を各々含み、残部Feおよび不可避的不純物からなる化学成分組成とする。なお、以下の元素含有量の単位は全て質量%だが、単に%と表記する場合もある。   For this reason, this invention steel material is the mass%, C: 0.08-0.61%, Si: 0.08-0.5%, Mn: 0.4-1.5%, P: 0.03 % Or less (excluding 0%), S: 0.005 to 0.1%, Cr: 0.4 to 2%, Al: 0.005 to 0.1%, N: 0.02% or less ( However, 0% is not included), and the chemical composition is composed of the remaining Fe and inevitable impurities. In addition, although the unit of the following element content is all the mass%, it may only describe with%.

ここで、本発明鋼材は、種々の特性を向上させるために、前記特定の化学成分組成に加えて、選択的な添加元素として、更に、質量%で、Ti:0.2%以下(但し0%を含まない)、Nb:0.2%以下(但し0%を含まない)、V:0.2%以下(但し0%を含まない)、B:0.01%以下(但し0%を含まない)、Mo:1%以下(但し0%を含まない)、Cu:1%以下(但し0%を含まない)、Ni:1%以下(但し0%を含まない)の1種又は2種以上を含有しても良い。また、これらに加えて、あるいはこれらの代わりに、Ca:0.02%以下(但し0%を含まない)、REM:0.02%以下(但し0%を含まない)、Li:0.02%以下(但し0%を含まない)、Mg:0.02%以下(但し0%を含まない)の1種又は2種以上を含有しても良い。   Here, in order to improve various properties, the steel material of the present invention is further added as a selective additive element in addition to the above specific chemical component composition, and further, by mass, Ti: 0.2% or less (however, 0 %), Nb: 0.2% or less (excluding 0%), V: 0.2% or less (excluding 0%), B: 0.01% or less (excluding 0%) 1) or less of Mo: 1% or less (excluding 0%), Cu: 1% or less (excluding 0%), Ni: 1% or less (excluding 0%) It may contain seeds or more. In addition to or in place of these, Ca: 0.02% or less (excluding 0%), REM: 0.02% or less (excluding 0%), Li: 0.02 % Or less (excluding 0%), Mg: 0.02% or less (excluding 0%), or one or more of them may be contained.

これら以外のその他の元素は、基本的には不純物であり、通常の、この種機械構造用の低炭素鋼材(肌焼き鋼)の不純物含有量 (許容量) レベルとする。   Other elements other than these are basically impurities, and the impurity content (allowable amount) level of a normal low carbon steel material (case-hardened steel) for this type of mechanical structure is used.

以下に、各主要元素の含有量と、その限定理由(意義)について説明する。   Below, content of each main element and its limitation reason (meaning) are demonstrated.

C:0.08〜0.61%
Cは、機械構造用部品としての必要強度を確保するための基本元素である。C含有量が少なすぎると、本発明が対象とする機械構造用部品に要求される強度を確保できない。しかし、Cを過剰に含有させると、延性を劣化させ、また鋼材が脆化し、衝撃特性が劣化する。このため、C含有量は0.08〜0.61%の範囲とし、下限値は好ましくは0.10%、より好ましくは0.13%とする。また、上限値は好ましくは0.58%、より好ましくは0.53%とする。
C: 0.08 to 0.61%
C is a basic element for ensuring the necessary strength as a machine structural component. If the C content is too small, the strength required for the machine structural component targeted by the present invention cannot be ensured. However, when C is contained excessively, ductility is deteriorated, the steel material becomes brittle, and impact characteristics deteriorate. Therefore, the C content is in the range of 0.08 to 0.61%, and the lower limit is preferably 0.10%, more preferably 0.13%. The upper limit is preferably 0.58%, more preferably 0.53%.

Si:0.08〜0.5%
Siは溶製中の鋼の脱酸作用に寄与する。また、固溶強化により母材強度を高める作用を有する。Si含有量が少なすぎると、脱酸が不十分となり、溶製時にガス欠陥が発生しやすくなる。また、本発明が対象とする機械構造用部品に要求される強度も確保できない。しかし、Siを過剰に含有させると、変形抵抗の増大や変形能の低下を生じさせる。この傾向はSi含有量が0.5%を超えると顕著に見られはじめる。このため、Si含有量は0.08〜0.5%の範囲とし、下限値は好ましくは0.10%、より好ましくは0.15%とする。また、上限値は好ましくは0.5%、より好ましくは0.4%とする。
Si: 0.08 to 0.5%
Si contributes to the deoxidizing action of steel during melting. Moreover, it has the effect | action which raises base material intensity | strength by solid solution strengthening. When there is too little Si content, deoxidation will become inadequate and it will become easy to generate | occur | produce a gas defect at the time of melting. Further, the strength required for the machine structural component targeted by the present invention cannot be ensured. However, when Si is contained excessively, an increase in deformation resistance and a decrease in deformability are caused. This tendency begins to be noticeable when the Si content exceeds 0.5%. Therefore, the Si content is in the range of 0.08 to 0.5%, and the lower limit is preferably 0.10%, more preferably 0.15%. The upper limit is preferably 0.5%, more preferably 0.4%.

Mn:0.4〜1.5%
Mnは、溶製中の鋼の脱酸、脱硫元素として有効であり、また、鋼材への熱間加工時の加工性の劣化を抑制する効果を有する。更に、Sと結合することで鋼材の変形能を向上させることにも有効である。Mn含有量が少なすぎると、これらの効果が得られず、変形能が劣化し、割れが生じやすくなる。一方で、Mnを過剰に含有させると、固溶強化による変形抵抗の増加と変形能の低下をもたらす。また、Pの粒界への偏析を助長し、粒界強度の低下、疲労強度の低下を生じさせる。このため、Mn含有量は0.4〜1.5%の範囲とし、下限値は好ましくは0.45%、より好ましくは0.5%とする。また、上限値は好ましくは1.2%、より好ましくは1.0%とする。
Mn: 0.4 to 1.5%
Mn is effective as a deoxidizing and desulfurizing element for steel during melting, and has an effect of suppressing deterioration of workability during hot working on steel. Furthermore, it is effective to improve the deformability of the steel material by combining with S. If the Mn content is too small, these effects cannot be obtained, the deformability is deteriorated, and cracking is likely to occur. On the other hand, when Mn is contained excessively, an increase in deformation resistance and a decrease in deformability due to solid solution strengthening are brought about. Moreover, segregation to the grain boundary of P is promoted, and the fall of grain boundary strength and the fall of fatigue strength are caused. Therefore, the Mn content is in the range of 0.4 to 1.5%, and the lower limit is preferably 0.45%, more preferably 0.5%. The upper limit is preferably 1.2%, more preferably 1.0%.

P:0.03%以下(但し0%を含まない)
Pは不可避的に混入し、不純物として含有する元素であり、フェライト粒界に偏析し、変形能を劣化させる。また、Pはフェライトを固溶強化させ、変形抵抗を増大させる。したがって、変形能の観点からPは極力低減することが望ましいが、極端な低減は製鋼コストの増加を招く。したがって、P含有量は0.03%以下の低いほど良いが、0%とすることは製造上困難であるので、0.03%以下(但し0%を含まない)と規定する。上限値は好ましくは0.025%、より好ましくは0.02%とする。
P: 0.03% or less (excluding 0%)
P is an element inevitably mixed in and contained as an impurity, segregates at the ferrite grain boundary, and deteriorates deformability. Further, P strengthens the solid solution of ferrite and increases the deformation resistance. Therefore, it is desirable to reduce P as much as possible from the viewpoint of deformability, but extreme reduction leads to an increase in steelmaking cost. Therefore, the lower the P content is, the better the content is 0.03% or less. However, since it is difficult to make it 0%, it is defined as 0.03% or less (but not including 0%). The upper limit is preferably 0.025%, more preferably 0.02%.

S:0.005〜0.1%
Sは被削性の向上効果があり、S含有量が少ないと被削性を劣化させる。ただ、Sは、Feと結合すると、FeSとして粒界上に膜状に析出するため、変形能を劣化させる。このため、Sは全量をMnと結合させ、MnSとして無害に析出させる必要がある。ただし、このMnSの析出量が増えると、やはり変形能が劣化する。したがって、S含有量は、変形能と被削性のバランスを考慮した、0.005〜0.1%の範囲とし、下限値は好ましくは0.007%、より好ましくは0.01%とし、上限値は好ましくは0.08%、より好ましくは0.06%とする。
S: 0.005-0.1%
S has an effect of improving machinability, and if the S content is small, the machinability is deteriorated. However, when S is combined with Fe, it precipitates in the form of a film on the grain boundary as FeS, so that the deformability is deteriorated. For this reason, S needs to be combined with Mn in its entirety, and be deposited harmlessly as MnS. However, as the amount of MnS deposited increases, the deformability also deteriorates. Accordingly, the S content is in the range of 0.005 to 0.1% considering the balance between deformability and machinability, and the lower limit is preferably 0.007%, more preferably 0.01%. The upper limit is preferably 0.08%, more preferably 0.06%.

Cr:0.4〜2%
Crは、鋼材の焼入れ性を高め、浸炭、窒化、浸炭窒化などの表面硬化処理による硬化層深さや、必要な母材硬さを与えることによって、歯車などの機械構造用部品としての静的強度および疲労強度を確保する上で重要な元素である。Cr含有量が少なすぎるとこうした効果を発揮できない一方で、Cr含有量が過剰になっても、旧オーステナイト粒界に炭化物として偏析するため、疲労強度、衝撃強度低下の原因となる。したがって、Cr含有量は0.4〜2%の範囲とし、下限値は好ましくは0.5%、より好ましくは0.6%とし、上限値は好ましくは1.8%、より好ましくは1.5%とする。
Cr: 0.4-2%
Cr enhances the hardenability of steel materials, and gives the hardened layer depth by surface hardening treatment such as carburizing, nitriding, carbonitriding, and the necessary base material hardness, thereby providing static strength as a mechanical structural component such as gears. It is an important element in ensuring fatigue strength. If the Cr content is too small, such effects cannot be exhibited. On the other hand, even if the Cr content is excessive, segregation as carbides occurs in the prior austenite grain boundaries, which causes a decrease in fatigue strength and impact strength. Accordingly, the Cr content is in the range of 0.4 to 2%, the lower limit is preferably 0.5%, more preferably 0.6%, and the upper limit is preferably 1.8%, more preferably 1.%. 5%.

Al:0.005〜0.1%
Alは溶製中の鋼の脱酸元素として有効である。Al含有量が少なすぎると、溶製中の脱酸が不十分となり、ガス欠陥が生じやすくなるので、割れが生じやすくなる。一方、Al含有量が過剰になっても、酸化アルミ系の酸化物などの非金属介在物が生成し、冷間加工性や被削性を劣化させる。したがって、Al含有量は0.005〜0.1%の範囲とし、下限値は好ましくは0.008%、より好ましくは0.01%とし、上限値は好ましくは0.08%、より好ましくは0.06%とする。
Al: 0.005 to 0.1%
Al is effective as a deoxidizing element for steel during melting. If the Al content is too small, deoxidation during melting becomes insufficient and gas defects are likely to occur, so that cracking is likely to occur. On the other hand, even if the Al content is excessive, non-metallic inclusions such as aluminum oxide-based oxides are generated, and cold workability and machinability are deteriorated. Therefore, the Al content is in the range of 0.005 to 0.1%, the lower limit is preferably 0.008%, more preferably 0.01%, and the upper limit is preferably 0.08%, more preferably 0.06%.

N:0.02%以下(但し0%を含まない)
Nは、摩擦圧接中に動的ひずみ時効を生じ、MnSの分解させるために必要な元素である。ただし、固溶状態で存在すると、熱間延性の劣化、動的ひずみ時効による冷間加工性や被削性の低下を招くため、予めAlなどと結合させて、AlNとして析出させておく必要がある。したがって、N含有量は0.02%以下(但し0%を含まない)の範囲とするが、Nが0.006%以下となると、冷間加工性や被削性は改善できるものの、MnSによる接合部、および熱影響部の強度劣化を抑制できなくなる可能性があるので、下限は、好ましくは0.006%以上、より好ましくは0.0065%以上、更に好ましくは0.0070%以上含有させる。上限値は、好ましくは0.018%、より好ましくは0.015%とする(いずれも0%を含まない)。
N: 0.02% or less (excluding 0%)
N is an element necessary for causing dynamic strain aging during friction welding and for decomposing MnS. However, when it exists in a solid solution state, it causes deterioration of hot ductility, cold workability and machinability due to dynamic strain aging, so it is necessary to preliminarily bond with Al and precipitate as AlN. is there. Accordingly, the N content is 0.02% or less (excluding 0%), but if N is 0.006% or less, cold workability and machinability can be improved, but MnS is used. The lower limit is preferably 0.006% or more, more preferably 0.0065% or more, and even more preferably 0.0070% or more, since there is a possibility that the strength deterioration of the joint and heat-affected zone may not be suppressed. . The upper limit is preferably 0.018%, more preferably 0.015% (both do not include 0%).

Ti:0.2%以下(但し0%を含まない)
Tiは、炭化物、窒化物を形成して、特にNを固定し、固溶Nによる変形能の劣化を防止し、オーステナイト粒の微細化、整粒化に寄与する。また、本発明においては、固溶Tiが残存できるだけのTiを含有させる必要がある。この固溶Tiは、前記した通り、摩擦圧接中にTiCを形成する。このTiCはオーステナイト粒を微細化、整粒化させると共に、析出強化に寄与する。そのため、摩擦圧接後の、熱影響部における強度の低下を抑制することができる。
Ti: 0.2% or less (excluding 0%)
Ti forms carbides and nitrides, particularly fixes N, prevents deterioration of deformability due to solute N, and contributes to austenite grain refinement and grain sizing. Moreover, in this invention, it is necessary to contain Ti which can remain solid solution Ti. This solute Ti forms TiC during friction welding as described above. This TiC contributes to precipitation strengthening while making austenite grains finer and sized. Therefore, it is possible to suppress a decrease in strength in the heat affected zone after the friction welding.

Ti含有量が少なすぎると、十分な量の固溶Tiを摩擦圧接時に作用させることができない。一方、Ti含有量が多すぎると、TiCが多量に生成するため、却って強度が低下する。したがって、Ti含有量は0.2%以下(但し0%を含まない)の範囲とし、下限値は好ましくは0.001%、より好ましくは0.01%、更に好ましくは0.015%とし、上限値は好ましくは0.15%、より好ましくは0.1%とする。   If the Ti content is too small, a sufficient amount of solute Ti cannot be applied during friction welding. On the other hand, when the Ti content is too large, a large amount of TiC is generated, and the strength is decreased. Therefore, the Ti content is in the range of 0.2% or less (excluding 0%), and the lower limit is preferably 0.001%, more preferably 0.01%, still more preferably 0.015%, The upper limit is preferably 0.15%, more preferably 0.1%.

Nb、V、Mo、Cu、Niの1種又は2種以上
Nb、V、Mo、Cu、Niは、前記特許文献5でも同効元素として記載している通り、いずれも、靱性を損なうことなく、素材としての鋼材や摩擦圧接後の複合鋼材の強度を向上させるのに有効である。
One or more of Nb, V, Mo, Cu, and Ni Nb, V, Mo, Cu, and Ni are all described as equivalent elements in Patent Document 5 without any loss of toughness. It is effective for improving the strength of steel as a raw material and composite steel after friction welding.

Nb:0.2%以下(但し0%を含まない)、V:0.2%以下(但し0%を含まない):Nb、Vは、いずれも炭化物などを形成し、摩擦圧接後の熱影響部における強度低下を抑制し、実質的に強度を向上させることができる。そこで、必要に応じて、Nb:0.2%以下(但し0%を含まない)、V:0.2%以下(但し0%を含まない)を添加する。   Nb: 0.2% or less (excluding 0%), V: 0.2% or less (excluding 0%): Nb and V both form carbides and heat after friction welding It is possible to suppress the strength reduction in the affected part and substantially improve the strength. Therefore, Nb: 0.2% or less (excluding 0%) and V: 0.2% or less (excluding 0%) are added as necessary.

選択的に添加する場合のNb含有量の下限は0.01%以上とすることが好ましく、0.015%以上とすることがより好ましい。一方、Nb含有量が多すぎるとNbCが多量に生成するため、逆に強度が低下する。したがって、Nb含有量の上限は0.15%以下とすることが好ましく、0.1%以下とすることがより好ましい。   The lower limit of the Nb content when selectively added is preferably 0.01% or more, and more preferably 0.015% or more. On the other hand, if the Nb content is too large, a large amount of NbC is generated, and the strength is reduced. Therefore, the upper limit of the Nb content is preferably 0.15% or less, and more preferably 0.1% or less.

選択的に添加する場合のV含有量の下限は0.01%以上とすることが好ましく、0.015%以上とすることがより好ましい。一方、V含有量が多すぎるとVCが多量に生成するため、逆に強度が低下する。したがって、V含有量の上限は0.15%以下とすることが好ましく、0.1%以下とすることがより好ましい。   The lower limit of the V content when selectively added is preferably 0.01% or more, and more preferably 0.015% or more. On the other hand, if the V content is too large, a large amount of VC is generated, and the strength is reduced. Therefore, the upper limit of the V content is preferably 0.15% or less, and more preferably 0.1% or less.

B:0.01%以下(但し0%を含まない)
Bは、鋼材の焼入れ性を向上させることに加えて、結晶粒界強化によって衝撃強度を高める作用を有する。B含有量が不足すると、これらの効果が得られず、一方で、B含有量が過剰になると、逆に粒界強度が低下し始めるので、冷間および熱間加工性が劣化する。したがって、B含有量は0.01%以下(但し0%を含まない)の範囲とし、下限値は好ましくは0.0005%、より好ましくは0.008%とし、上限値は好ましくは0.008%、より好ましくは0.005%とする。
B: 0.01% or less (excluding 0%)
In addition to improving the hardenability of the steel material, B has the effect of increasing the impact strength by strengthening the grain boundaries. If the B content is insufficient, these effects cannot be obtained. On the other hand, if the B content is excessive, the grain boundary strength starts to decrease, so that the cold and hot workability deteriorates. Therefore, the B content is in the range of 0.01% or less (excluding 0%), the lower limit is preferably 0.0005%, more preferably 0.008%, and the upper limit is preferably 0.008. %, More preferably 0.005%.

Mo:1%以下(但し0%を含まない)
Moは、鋼材の焼入れ性を確保して、不完全焼入れ組織の生成を抑制し、強度を向上させるのに有効な元素である。そこで、必要に応じて、Mo:1%以下(但し0%を含まない)を添加する。一方、Moの含有量が過剰になると、母材の硬度が必要以上に硬くなって靭性、衝撃特性が劣化するので、1%以下に限って、好ましくは0.8%以下、より好ましくは0.5%以下添加する。なお、Moによる前記効果を有効に発揮させるためには、0.06%以上の添加が好ましく、より好ましくは0.08%以上添加する。
Mo: 1% or less (excluding 0%)
Mo is an element effective for securing the hardenability of the steel material, suppressing the formation of an incompletely quenched structure, and improving the strength. Therefore, if necessary, Mo: 1% or less (but not including 0%) is added. On the other hand, if the Mo content is excessive, the hardness of the base material becomes unnecessarily hard and the toughness and impact properties deteriorate, so only 1% or less, preferably 0.8% or less, more preferably 0. Add less than 5%. In addition, in order to exhibit the said effect by Mo effectively, addition of 0.06% or more is preferable, More preferably, 0.08% or more is added.

Cu、Ni
Cu、Niはいずれも鋼材を固溶強化させ、母材や接合部分の強度を向上させるのに有効である。そこで、必要に応じて、Cu:1%以下(但し0%を含まない)、Ni:1%以下(但し0%を含まない)を添加する。一方、Cu、Niの含有量が過剰になると熱間延性が劣化するので、各々1%以下に限って、好ましくは各々0.8%以下、より好ましくは各々0.6%以下添加する。なお、Cu、Niによる前記効果を有効に発揮させるためには、0.2%以上の添加が好ましく、より好ましくは各々0.3%以上添加する。
Cu, Ni
Both Cu and Ni are effective in strengthening the solid solution of the steel material and improving the strength of the base material and the joint portion. Therefore, Cu: 1% or less (excluding 0%) and Ni: 1% or less (excluding 0%) are added as necessary. On the other hand, if the Cu and Ni contents are excessive, the hot ductility deteriorates, so each is limited to 1% or less, preferably 0.8% or less, more preferably 0.6% or less. In order to effectively exhibit the above-described effects due to Cu and Ni, addition of 0.2% or more is preferable, and more preferably 0.3% or more is added.

Ca、REM、Li、Mgの1種又は2種以上
Ca、REM、Li、Mgは、共通して、MnS等の硫化化合物系介在物を球状化させ、鋼材の変形能を高めると共に、冷間加工性や被削性向上に寄与する元素である。そこで、必要に応じて、Ca:0.02%以下(但し0%を含まない)、REM:0.02%以下(但し0%を含まない)、Li:0.005%以下(但し0%を含まない)、Mg:0.005%以下(但し0%を含まない)の1種又は2種以上を添加する。
One or more of Ca, REM, Li, and Mg Ca, REM, Li, and Mg are commonly used to spheroidize sulfide compound inclusions such as MnS to improve the deformability of the steel material, It is an element that contributes to improving workability and machinability. Therefore, as necessary, Ca: 0.02% or less (excluding 0%), REM: 0.02% or less (excluding 0%), Li: 0.005% or less (providing 0%) 1) or 2 or more of Mg: 0.005% or less (excluding 0%).

前記効果を有効に発揮させるためには、Ca、REMは0.0005%以上の添加が好ましく、より好ましくは各々0.001%以上、更に好ましくは各々0.0015%以上添加する。同じく、Li、Mgは0.0001%以上の添加が好ましく、より好ましくは各々0.0002%以上、更に好ましくは各々0.0003%以上添加する。一方、これらを過剰に添加してもその効果が飽和し、添加量に見合う効果が期待できず経済的に不利である。そのため、Ca、REMは各々0.01%以下の添加が好ましく、より好ましくは各々0.005%以下添加する。同じく、Li、Mgは各々0.0025%以下の添加が好ましく、より好ましくは各々0.001%以下添加する。   In order to effectively exhibit the above effects, Ca and REM are preferably added in an amount of 0.0005% or more, more preferably 0.001% or more, and still more preferably 0.0015% or more. Similarly, Li and Mg are preferably added in an amount of 0.0001% or more, more preferably 0.0002% or more, and still more preferably 0.0003% or more. On the other hand, even if these are added excessively, the effect is saturated, and an effect commensurate with the amount added cannot be expected, which is economically disadvantageous. Therefore, Ca and REM are each preferably added in an amount of 0.01% or less, more preferably 0.005% or less. Similarly, Li and Mg are each preferably added in an amount of 0.0025% or less, more preferably 0.001% or less.

Nの存在形態制御
本発明では、摩擦圧接の前後で鋼中のNの存在形態を変化させ、摩擦圧接後の接合強度の向上と、冷間加工性や被削性の向上という、相矛盾する技術課題を解決する。すなわち、摩擦圧接の前に、素材低炭素鋼材の鋼中のNの多くを化合物Nとして存在させるとともに、固溶Nとしての存在量を規制する。これによって、素材としての低炭素鋼材や摩擦圧接されて複合鋼としての低炭素鋼材の冷間加工性や被削性を向上させる。
In the present invention, there is a contradiction in that the presence form of N in the steel is changed before and after the friction welding to improve the joint strength after the friction welding and to improve the cold workability and machinability. Solve technical issues. That is, before friction welding, most of N in the steel of the raw material low carbon steel is present as the compound N, and the abundance as the solid solution N is regulated. This improves the cold workability and machinability of the low carbon steel material as a raw material and the low carbon steel material as a composite steel by friction welding.

素材低炭素鋼材をこのように予め準備することによって、摩擦圧接の際の摩擦熱によって、摩擦圧接後の低炭素鋼材における熱影響部の、鋼中の化合物Nを分解させ、固溶N量を増量させる。そして、この固溶Nによる動的ひずみ時効によって、前記熱影響部のフェライトあるいはオーステナイト(セメンタイト)を固溶強化し、前記熱影響部の過度の強度低下や、接合部分の過度の強度増加を抑制して、摩擦圧接後の接合強度を向上させる。   By preparing the raw material low carbon steel material in advance in this way, the compound N in the steel of the heat affected zone in the low carbon steel material after friction welding is decomposed by the friction heat at the time of friction welding, and the amount of solid solution N is reduced. Increase the dose. And, by dynamic strain aging with this solid solution N, ferrite or austenite (cementite) of the heat affected zone is solid solution strengthened, and excessive strength decrease of the heat affected zone and excessive strength increase of the joined portion are suppressed. Thus, the bonding strength after friction welding is improved.

また、摩擦圧接の前後で、このようにNの存在形態を変化させることによって、摩擦圧接の前後で、鋼中に存在するMnSの形状も変化させることができ、N制御との相乗効果で、摩擦圧接後の接合強度の向上と、冷間加工性や被削性の向上を更に図ることができる。   Also, by changing the form of N in this way before and after friction welding, the shape of MnS present in the steel can be changed before and after friction welding, with a synergistic effect with N control, It is possible to further improve the joint strength after friction welding and improve the cold workability and machinability.

化合物N
本発明では、前記した通り、摩擦圧接の前の低炭素鋼材における化合物N(化合物窒素)量を増加させる。素材低炭素鋼材の化合物N量が少なすぎれば、摩擦圧接後の低炭素鋼材における熱影響部の鋼中の化合物Nの分解により生成する、固溶N量も少なくなる。この結果、固溶Nによる動的ひずみ時効によって、前記熱影響部のフェライトあるいはオーステナイト(セメンタイト)を固溶強化し、前記熱影響部の過度の強度低下や、接合部分の過度の強度増加を抑制する効果も弱まる。この結果、摩擦圧接後の接合強度を向上させることができなくなる。
Compound N
In the present invention, as described above, the amount of compound N (compound nitrogen) in the low carbon steel material before friction welding is increased. If the amount of compound N in the raw low carbon steel material is too small, the amount of solid solution N generated by decomposition of compound N in the steel in the heat-affected zone in the low carbon steel material after friction welding is also reduced. As a result, due to dynamic strain aging with solid solution N, ferrite or austenite (cementite) in the heat affected zone is solid solution strengthened, and excessive strength decrease in the heat affected zone and excessive increase in strength in the bonded portion are suppressed. The effect to do is also weakened. As a result, it becomes impossible to improve the bonding strength after friction welding.

また、素材低炭素鋼材の化合物N量が少なすぎれば、摩擦圧接後の、この固溶N量の減少に伴い、固溶Nによる動的ひずみ時効に伴う、MnS周囲のフェライトあるいはオーステナイト(セメンタイト)の前記固溶強化も弱まる。このため、予め存在する一定のサイズの伸長した形状のMnSを細かく分断して微細化させる効果も弱まる。この結果、微細化されたMnSによる、前記熱影響部のオーステナイト粒径の整粒効果や前記熱影響部の強度劣化への影響(寄与)をなくす効果も弱まる。   Also, if the amount of compound N in the low-carbon steel material is too small, ferrite or austenite (cementite) around MnS accompanying dynamic strain aging due to solid solution N as the amount of solid solution N decreases after friction welding. The solid solution strengthening is also weakened. For this reason, the effect of finely dividing MnS having a certain size and having an elongated shape to be finely divided is weakened. As a result, the effect of eliminating the influence (contribution) of the refined MnS on the austenite grain size adjusting effect of the heat affected zone and the strength deterioration of the heat affected zone is weakened.

ただ、化合物N量があまり多すぎれば、却って、摩擦圧接後の接合強度が低下する。このため、鋼中の化合物Nの含有量は0.006〜0.02%の範囲とする。   However, if the amount of compound N is too large, the bonding strength after friction welding is lowered. For this reason, content of the compound N in steel shall be 0.006 to 0.02% of range.

素材低炭素鋼材をこのように予め準備することによって、摩擦圧接の際の摩擦熱によって、摩擦圧接後の低炭素鋼材における熱影響部の、鋼中の化合物Nを分解させ、固溶N量を増量させる。そして、この固溶Nによる動的ひずみ時効によって、前記熱影響部のフェライトあるいはオーステナイト(セメンタイト)を固溶強化し、前記熱影響部の強度低下や、接合部分の過度の強度増加を抑制して、摩擦圧接後の接合強度を向上させる。   By preparing the raw material low carbon steel material in advance in this way, the compound N in the steel of the heat affected zone in the low carbon steel material after friction welding is decomposed by the friction heat at the time of friction welding, and the amount of solid solution N is reduced. Increase the dose. And by the dynamic strain aging by this solid solution N, the ferrite or austenite (cementite) of the heat affected zone is solid solution strengthened, and the strength reduction of the heat affected zone and the excessive increase of the strength of the joined portion are suppressed. , Improve the bonding strength after friction welding.

化合物N(化合物窒素)は、前記した通り、鋼中の全N(全窒素)のうち、固溶Nを除く、窒化物や炭窒化物などの化合物を形成して鋼中に存在するN(窒素)であり、後述するアンモニア蒸留分離インドフェノール青吸光光度法により、直接測定できる。   As described above, the compound N (compound nitrogen) is a compound such as a nitride or carbonitride that excludes solid solution N out of all N (total nitrogen) in the steel and exists in the steel ( Nitrogen) and can be directly measured by the ammonia distillation separation indophenol blue absorptiometry described later.

化合物N量の測定
前記化合物N量の測定は、アンモニア蒸留分離インドフェノール青吸光光度法により行う。すなわち、鋼供試材から切り出したサンプル約0.5を、10%AA系電解液に定電流電解を行って溶解させ、生成する不溶解残渣(窒化化合物)を穴サイズが0.1μmのポリカーボネート製のフィルタでろ過する。得られた不溶解残渣を、硫酸、硫酸カリウムおよび純銅製チップ中で加熱して分解し、分解物をろ液に合わせる。この溶液を、水酸化ナトリウムでアルカリ性にした後、水蒸気蒸留を行い、留出したアンモニアを希硫酸に吸収させる。更に、フェノール、次亜塩素酸ナトリウムおよびペンタシアノニトロシル鉄(III )酸ナトリウムを加えて青色錯体を生成させ、吸光光度計を用いて吸光度を測定して、前記化合物量を求める。因みに、前記10%AA系電解液は、10%アセトン、10%塩化テトラメチルアンモニウム、残部メタノールからなる非水溶媒系の電解液であり、鋼表面に不動態皮膜を生成させない溶液である。
Measurement of the amount of Compound N The amount of Compound N is measured by ammonia distillation separation indophenol blue absorptiometry. That is, about 0.5 sample cut from a steel specimen was dissolved in 10% AA electrolyte by constant current electrolysis, and the resulting insoluble residue (nitride compound) was polycarbonate having a hole size of 0.1 μm. Filter with a made filter. The obtained insoluble residue is decomposed by heating in a chip made of sulfuric acid, potassium sulfate and pure copper, and the decomposition product is combined with the filtrate. After making this solution alkaline with sodium hydroxide, steam distillation is performed, and the distilled ammonia is absorbed in dilute sulfuric acid. Further, phenol, sodium hypochlorite and sodium pentacyanonitrosyl iron (III) are added to form a blue complex, and the absorbance is measured using an absorptiometer to determine the amount of the compound. Incidentally, the 10% AA electrolyte solution is a non-aqueous solvent electrolyte solution consisting of 10% acetone, 10% tetramethylammonium chloride, and the remaining methanol, and does not generate a passive film on the steel surface.

固溶N
前記化合物Nに対して、本発明では、鋼中の固溶N量を十分に低減することで、素材としての低炭素鋼材や摩擦圧接されて複合鋼としての低炭素鋼材の冷間加工性や被削性を向上させる。このため、鋼中の固溶N量は0.0015%以下(但し0%を含む)に規制する。鋼中の固溶N量が0.0015%を超えた場合、低炭素鋼材の冷間加工性や被削性を向上できず、接合強度向上との兼備ができない。
Solid solution N
With respect to the compound N, in the present invention, by sufficiently reducing the amount of solute N in the steel, the cold workability of the low carbon steel material as a raw material or the low carbon steel material as a composite steel by friction welding, Improves machinability. For this reason, the amount of solute N in the steel is regulated to 0.0015% or less (including 0%). When the amount of solute N in the steel exceeds 0.0015%, the cold workability and machinability of the low carbon steel material cannot be improved, and the joint strength cannot be improved.

このように、予め低炭素鋼材の固溶N量を低減しても、摩擦圧接後の低炭素鋼材における熱影響部では、鋼中の化合物Nを分解させ、固溶N量を増量させることができ、摩擦圧接後の接合強度を向上させられることが、本発明の大きな特徴である。   Thus, even if the solute N amount of the low carbon steel material is reduced in advance, in the heat-affected zone in the low carbon steel material after friction welding, the compound N in the steel can be decomposed to increase the solute N amount. It is possible to improve the bonding strength after friction welding, which is a great feature of the present invention.

この固溶Nの含有量は、JISG1228に準拠して、下記方法によって求められる全N量から、上記方法によって求められた全化合物N量を差し引いて、間接的に求めることができる。   The content of the solid solution N can be obtained indirectly by subtracting the total amount of compound N obtained by the above method from the total amount of N obtained by the following method in accordance with JISG1228.

前記全N量の測定は、不活性ガス融解法−熱伝導度法により、鋼供試材から切り出したサンプルをルツボに入れ、不活性ガス気流中で融解してNを抽出し、この抽出物を熱伝導度セルに搬送して、熱伝導度の変化を測定する。そして、予め求めておいた熱伝導度と全N量との関係から全N量を求める。   The total amount of N is measured by inert gas melting method-thermal conductivity method. A sample cut from a steel specimen is put in a crucible and melted in an inert gas stream to extract N, and this extract Is transferred to the thermal conductivity cell and the change in thermal conductivity is measured. Then, the total N amount is determined from the relationship between the thermal conductivity determined in advance and the total N amount.

低炭素鋼材のMnS
本発明では、低炭素鋼材の被削性の向上のために、一定の大きなサイズの伸長したMnSを存在させる。すなわち、低炭素鋼材の鋼中に、最大長さが2μm以上のMnSを1mm2 当たり100〜4000個存在させ、かつ、これらのMnSの平均アスペクト比を2以上とする。ここで、アスペクト比とは、不定形のMnS粒子における、最大長さ(最も長い軸あるいは最も長い辺の軸長さ)と、最小長さ(最も短い軸あるいは最も短い辺の軸の長さ)との比、最大長さ/最小長さ、である。そして、アスペクト比が大きいほど、MnSは、アスペクト比が1の等軸ではなく、伸張した(偏平あるいは細長い)形状となる。
Low carbon steel MnS
In the present invention, in order to improve the machinability of the low carbon steel material, elongated MnS having a certain large size is present. That is, 100 to 4000 MnS having a maximum length of 2 μm or more per 1 mm 2 are present in the steel of the low carbon steel material, and the average aspect ratio of these MnS is set to 2 or more. Here, the aspect ratio refers to the maximum length (longest axis or longest side axis length) and minimum length (shortest or shortest side axis length) of amorphous MnS particles. Ratio, maximum length / minimum length. As the aspect ratio increases, the MnS has an elongated shape (flat or elongated) rather than an equiaxed aspect ratio of 1.

低炭素鋼材の被削性を向上させるためには、MnSの形状と含有量が重要となる。接合部および熱影響部の強度(靭性)を確保するためには、MnSの量を減らすことが有効であるが、MnS量を少なくすると、十分な被削性を得ることができない。   In order to improve the machinability of the low carbon steel material, the shape and content of MnS are important. In order to secure the strength (toughness) of the joint and the heat-affected zone, it is effective to reduce the amount of MnS. However, if the amount of MnS is reduced, sufficient machinability cannot be obtained.

この点で、機械構造用の低炭素鋼材に、Sを添加して、一定の大きさ(長さ)以上で、形状的にも最大長さと最小長さとの比であるアスペクト比が大きな、伸張した形状のMnSを増加させれば、接合部および熱影響部の強度(靭性)を低下させることなく、被削性が向上する。一定の大きさ(長さ)以上で、アスペクト比が大きな伸張形状のMnSの増加は、切削中の切削抵抗を低減すると共に、切り屑分断性を向上させるため、被削性の向上に有効である。最大長さ(最も長い辺の長さ)が2μm以上のMnSの個数を1mm2 当たり100個以上、これら最大長さが2μm以上のMnSの平均アスペクト比を2以上、とすることで、切削中の切屑を容易に分断させることができるようになる。 In this regard, S is added to a low carbon steel material for mechanical structures, and the aspect ratio, which is the ratio of the maximum length to the minimum length in terms of shape, is greater than the certain size (length). If the MnS having the above shape is increased, the machinability is improved without reducing the strength (toughness) of the joint and the heat affected zone. An increase in stretched MnS with a certain size (length) or more and a large aspect ratio is effective in improving machinability because it reduces cutting resistance during cutting and improves chip breaking. is there. During cutting, the number of MnS with a maximum length (longest side length) of 2 μm or more is 100 or more per mm 2 , and the average aspect ratio of MnS with a maximum length of 2 μm or more is 2 or more. It becomes possible to easily sever the chips.

アスペクト比が2未満、最大長さ(最も長い軸あるいは最も長い辺の軸長さ)が2μm未満のMnSの増加は、却って、切屑が分断しにくくなり、切削効率が劣化する。すなわち、微細でアスペクト比が小さなMnSの増加は、被削性の向上に効果がないどころか、却って被削性を低下させる。したがって、素材低炭素鋼材の鋼中で、摩擦圧接に先立って、予め増加させるMnSは、後述する倍率400倍の光学顕微鏡を用いた測定方法で観察される、不定形のMnS粒子において、最大長さが2μm以上である、伸張した形状の(偏平あるいは細長い)MnSで、且つ、平均アスペクト比が2以上のMnSとする。   If the aspect ratio is less than 2 and the maximum length (longest axis or longest side axis length) is less than 2 μm, the increase in MnS makes it difficult for the chips to be cut and the cutting efficiency deteriorates. That is, the increase in MnS having a small aspect ratio is not effective in improving the machinability but rather lowers the machinability. Accordingly, in the steel of the low carbon steel material, MnS that is increased in advance prior to the friction welding is the maximum length in the amorphous MnS particles that are observed by a measurement method using an optical microscope with a magnification of 400 times described later. The MnS is a stretched (flat or elongated) MnS having an average aspect ratio of 2 or more.

なお、これらMnSの形状は、大きく伸張すれば、それだけ被削性が改善されるが、製造条件による最大長さの製造限界も当然あるので、最大長さの上限は好ましくは100μm以下、平均アスペクト比の上限は好ましくは10以下と各々する。   It should be noted that the machinability of these MnS shapes is improved as much as they are extended, but there is naturally a production limit of the maximum length depending on the production conditions, so the upper limit of the maximum length is preferably 100 μm or less, and the average aspect ratio The upper limit of the ratio is preferably 10 or less.

また、このような一定の大きさ(長さ)以上で、かつアスペクト比が大きなMnSであっても、多すぎると、鋼材を摩擦圧接した場合に、MnSは摩擦圧接中に鋼材がバリとして排出される過程において、圧接方向に対して垂直方向に偏向するようになる。このようなMnSは接合部、あるいは熱影響部における靭性を著しく劣化させる。したがって、本発明では、接合部および熱影響部の強度(靭性)を確保するために、また、鋼材の靭性の劣化や鋼材圧延時の割れを防止するため、アスペクト比が2以上の伸張した形状で、且つ、最大長さが2μm以上のMnSの鋼中に存在させる量(数)の上限を定める。すなわち、このようなMnSの鋼中に存在させる量(数)の上限は4000個/mm2 とする。 Further, even if MnS is a certain size (length) or more and has a large aspect ratio, if it is too much, MnS is discharged as burrs during friction welding when steel is friction welded. In the process, the light is deflected in the direction perpendicular to the pressure contact direction. Such MnS significantly deteriorates the toughness at the joint or heat-affected zone. Therefore, in the present invention, in order to ensure the strength (toughness) of the joint and the heat-affected zone, and to prevent the deterioration of the toughness of the steel material and cracking during the rolling of the steel material, the elongated shape having an aspect ratio of 2 or more. And the upper limit of the amount (number) to be present in the steel of MnS having a maximum length of 2 μm or more. That is, the upper limit of the amount (number) of MnS present in the steel is 4000 pieces / mm 2 .

摩擦圧接部品のMnS
このように、素材(摩擦圧接前の)低炭素鋼材では伸長した形状のMnSを存在させるが、摩擦圧接部品では、前記熱影響部の強度劣化へ影響(寄与)するMnSを逆に規制することが、また本発明の特徴でもある。
MnS for friction welding parts
In this way, the low-carbon steel material (before friction welding) causes MnS having an elongated shape to exist, but in the friction welding parts, MnS that affects (contributes) to the strength deterioration of the heat-affected zone is restricted. Is also a feature of the present invention.

具体的には、前記摩擦圧接によって形成された接合部から1mm幅の範囲の低炭素鋼材側の熱影響部の鋼中における、アスペクト比が2以下で、且つ、最大長さが1μm以下のMnSを、1mm2 当たり25個以下(但し0個を含む)に規制する。但し、このような微細なMnSであれば、後述する400倍の光学顕微鏡による測定では、当然測定限界はあるので、最大長さの下限は、この光学顕微鏡による測定で、長さが個数が測定可能な限界の長さとする。また、この光学顕微鏡で測定できないような微細なMnSであれば、前記熱影響部の強度劣化へ影響(寄与)しない。 Specifically, the MnS having an aspect ratio of 2 or less and a maximum length of 1 μm or less in the steel of the heat affected zone on the low carbon steel material side in the range of 1 mm width from the joint formed by the friction welding. Is regulated to 25 or less (including 0) per 1 mm 2 . However, with such a fine MnS, there is of course a measurement limit in the measurement with a 400 × optical microscope, which will be described later, so the lower limit of the maximum length is measured with this optical microscope, and the number is measured in length. The possible limit length. Moreover, if it is fine MnS which cannot be measured with this optical microscope, it does not influence (contribute) to the strength deterioration of the heat affected zone.

そして、このような熱影響部のMnS規制は、前記した通り、素材(摩擦圧接前の)低炭素鋼材に予め化合物Nを含有させ、この化合物Nを、摩擦圧接の際の摩擦熱によって分解させて、摩擦圧接後の低炭素鋼材における熱影響部の固溶N量を増量させることによって可能である。前記最大長さが1μm以下のMnSとは、前記固溶Nによる動的ひずみ時効に伴う、MnS周囲のフェライトあるいはオーステナイト(セメンタイト)の前記強化によって、摩擦圧接による強ひずみ加工とも相まって、予め存在する一定のサイズの伸長した形状のMnSが細かく分断されたものである。   And as described above, the MnS regulation of such a heat-affected zone includes compound N in advance in a raw material (before friction welding), and decomposes this compound N by frictional heat during friction welding. Thus, it is possible to increase the amount of solute N in the heat-affected zone in the low carbon steel material after friction welding. The MnS having a maximum length of 1 μm or less is preliminarily present in combination with strong strain processing by friction welding due to the strengthening of ferrite or austenite (cementite) around MnS accompanying dynamic strain aging by the solid solution N. An elongated shape of MnS having a certain size is finely divided.

このように分断、分解されたMnSは、前記した通り、前記熱影響部のオーステナイト粒径の整粒化に寄与するが、あまり多すぎれば、却って、摩擦圧接後の接合強度が低下する。このため、前記規定通りに規制する。   The MnS thus divided and decomposed contributes to the austenite grain size regulation of the heat-affected zone as described above. However, if it is too much, the bonding strength after friction welding is lowered. For this reason, it regulates according to the above-mentioned regulation.

なお、前記熱影響部の幅は、勿論、前記摩擦圧接の条件によって異なるが、通常の摩擦圧接の条件によれば、前記摩擦圧接の接合部から1mm以上の幅を通常は必ず、十分に有する。したがって、測定の再現性の点からも、前記摩擦圧接の接合部から1mm幅の範囲の低炭素鋼材側の熱影響部と規定した。   Of course, the width of the heat-affected zone varies depending on the friction welding conditions. However, according to the normal friction welding conditions, the width of 1 mm or more from the joint of the friction welding is usually always sufficient. . Therefore, also from the point of reproducibility of measurement, it was defined as a heat affected zone on the low carbon steel material side in a range of 1 mm width from the joint portion of the friction welding.

NやMnSの存在形態と特性との関係
ここで、改めてNやMnSの存在形態と特性との関係を説明する。本発明者らが、各種成分を調整した鋼材を用いて摩擦圧接実験を行った結果、摩擦圧接後の接合部付近(接合部から1mm幅の範囲)の固溶N量が高い鋼材は、接合部および熱影響部の強度(靭性)が十分確保されることが明らかとなった。
Relationship between N and MnS Presence Form and Properties Here, the relationship between N and MnS existence form and properties will be described again. As a result of the inventors performing a friction welding experiment using steel materials with various components adjusted, a steel material having a high solute N amount in the vicinity of the joint after friction welding (in the range of 1 mm width from the joint) is It was revealed that the strength (toughness) of the heat affected zone and the heat affected zone is sufficiently secured.

その組織は、接合部付近で初期のような伸張した形状のMnSが観察されず、また、結晶粒も整粒化していた。これは、摩擦圧接中に固溶NがMnSの分解に寄与していることによると考えることができた。但し、このような固溶N量の高い鋼材は、冷間加工性や被削性が劣化しており、冷間加工性や被削性と、接合部および熱影響部の強度とを両立させることが困難であった。   In the structure, no elongated MnS as in the initial stage was observed in the vicinity of the joint, and the crystal grains were also sized. This could be attributed to the fact that solute N contributes to the decomposition of MnS during friction welding. However, such a steel material with a high solute N content has deteriorated cold workability and machinability, and achieves both the cold workability and machinability and the strength of the joint and the heat affected zone. It was difficult.

上記実験結果に基づき、摩擦圧接前後でNの存在形態を変化させることが有効であることを知見し、摩擦圧接前の鋼材成分と組織を、冷間加工性や被削性に優れるように調整し、且つ、勿論摩擦圧接条件を通常通り適正化することで、摩擦圧接中に固溶N量を増加させ、接合部、および熱影響部の強度を向上させることができた。   Based on the above experimental results, we learned that it is effective to change the form of N before and after friction welding, and adjusted the steel composition and structure before friction welding to be excellent in cold workability and machinability. And of course, by optimizing the friction welding conditions as usual, the amount of solute N was increased during the friction welding, and the strength of the joint and the heat affected zone could be improved.

すなわち、摩擦圧接中に鋼材の接合部および熱影響部に十分に入熱される条件で摩擦圧接を行い、化合物N(N化合物)を分解させ、固溶N量を増量させる。そして、この固溶Nによる動的ひずみ時効によって、MnS周囲のフェライト、あるいはオーステナイト(セメンタイト)が強化され、摩擦圧接による強ひずみ加工に伴って、伸長したMnSも分断されやすくなることも知見した。このように十分に分解されたMnSは、オーステナイト粒径の整粒化に寄与し、且つ、強度劣化には影響(寄与)しなくなる効果を有する。   That is, friction welding is performed under conditions where heat is sufficiently input to the joint and heat-affected zone of the steel material during friction welding to decompose compound N (N compound) and increase the amount of solid solution N. It was also found that the dynamic strain aging caused by the solute N strengthens the ferrite or austenite (cementite) around the MnS, and the elongated MnS tends to be divided along with the high strain processing by friction welding. MnS sufficiently decomposed in this way contributes to the austenite grain size regulation and has the effect of not affecting (contributing) to the strength deterioration.

以上の通り摩擦圧接によって靭性の劣化を抑制した部材に、浸炭、焼戻し熱処理などを施すことによって、摩擦接合部品の欠点であった、曲げ特性、衝撃特性の低下を抑制した部品とすることができる。また、肌焼鋼としての面疲労特性、冷間加工性や被削性に関しても、それぞれ特性を満足させることができる。   As described above, by performing carburization, tempering heat treatment, etc., on a member that has suppressed toughness degradation by friction welding, it is possible to obtain a component that suppresses a decrease in bending characteristics and impact characteristics, which was a drawback of friction bonded parts. . Moreover, regarding the surface fatigue characteristics, cold workability and machinability as case hardening steel, the respective characteristics can be satisfied.

鋼材の組織
本発明鋼材の組織は、摩擦圧接に適した組織とするために、また、摩擦接合部品としての特性を満たすために、フェライト粒とパーライト粒との混相からなるものとする。因みに、摩擦圧接による接合部の組織は、急速加熱と急速冷却によって、一部がベイナイトとなった、マルテンサイト相で構成される。このようなベイナイトは、前記マルテンサイトと比較して硬さが低いため、接合部の強度増加を抑制することができ、また、衝撃特性、疲労特性を向上させることができる。
The structure of the steel material The structure of the steel material of the present invention is composed of a mixed phase of ferrite grains and pearlite grains in order to obtain a structure suitable for friction welding and to satisfy the characteristics as a friction bonded part. Incidentally, the structure of the joint by friction welding is composed of a martensite phase that is partially bainite by rapid heating and rapid cooling. Since such bainite has a lower hardness than the martensite, it can suppress an increase in strength of the joint and can improve impact characteristics and fatigue characteristics.

鋼材の製造方法
なお、機械構造用低炭素鋼材自体は、フェライト粒とパーライト粒との混相組織も含めて、通常の前記自動車部品用の機械構造用鋼材の製造工程で製造できる。即ち、鋳造されたインゴット(鋳塊)をビレット(鋼片)に熱間鍛造後、熱間圧延あるいは熱間鍛造によって、線材や棒材(丸棒、角棒)などの鋼材に加工される。
Manufacturing method of steel material In addition, the low-carbon steel material itself for machine structure can be manufactured in the manufacturing process of the said steel material for machine structures for motor vehicle parts including the mixed phase structure of a ferrite grain and a pearlite grain. That is, a cast ingot (ingot) is hot-forged into a billet (steel piece) and then processed into a steel material such as a wire rod or rod (round bar, square bar) by hot rolling or hot forging.

但し、本発明鋼材は、これら熱間圧延上がり、あるいは熱間鍛造上がりの鋼材(熱間加工まま材)、あるいは更に冷間鍛造などによって部品形状に形成された鋼材、これらを更に精密な切削・仕上げ加工された機械構造部品(機械構造部品とされた鋼材)であっても良い。 However, the steel material of the present invention is a steel material that has been hot-rolled or hot-forged (as it is hot-worked), or a steel material that has been formed into a part shape by cold forging. It may be a machine-structured part (steel material made into a machine-structured part) that has been finished.

ここで、本発明において規定した、鋼中の化合物Nの含有量を確保し、固溶N量、伸長したMnSの数とアスペクト比を制御するためには、成分を適正に調整し、且つ、前記ビレットの熱間圧延前の加熱温度と、線材や棒材への熱間圧延温度とを合わせて制御する。 すなわち、前記ビレットの加熱温度を1000〜1250℃の範囲で行うとともに、前記ビレットの圧延開始から線材や棒材への圧延終了までの熱間圧延の温度を800〜1000℃の範囲で行う。   Here, in order to secure the content of the compound N in the steel defined in the present invention and control the amount of solid solution N, the number of elongated MnS and the aspect ratio, the components are adjusted appropriately, and The heating temperature before hot rolling of the billet and the hot rolling temperature to the wire or bar are controlled together. That is, the heating temperature of the billet is in the range of 1000 to 1250 ° C., and the hot rolling temperature from the start of rolling the billet to the end of rolling to the wire or rod is in the range of 800 to 1000 ° C.

前記ビレットの加熱温度や熱間圧延温度を適正に制御することで、伸長したMnSとなりやすく、伸長したMnSの数とアスペクト比を確保することができる。   By appropriately controlling the heating temperature and hot rolling temperature of the billet, it becomes easy to become elongated MnS, and the number and aspect ratio of elongated MnS can be ensured.

ただし、上記のような高温加熱、高温圧延では、Nが全数固溶状態で存在するため、冷却後、被削性を劣化させる問題が生じる。そこで、冷却速度を適正に制御することで、冷却中に固溶NをAlと結合させ、AlNとして析出させることで、固溶Nを固定し、低減することができる。そのための冷却速度としては、上記熱間圧延や熱間鍛造終了後は、室温までの冷却速度を2.0℃/秒以下として冷却することが好ましい。この冷却速度で冷却することによって、冷却中に固溶NをAlと結合させ、AlNとして析出させることで、固溶Nを低減することができる。また、鋼材組織も、より切削に適したフェライト粒とパーライト粒との混相とすることができる。   However, in the high-temperature heating and high-temperature rolling as described above, since N is present in a solid solution state, there arises a problem that the machinability is deteriorated after cooling. Therefore, by appropriately controlling the cooling rate, solid solution N is combined with Al during cooling and precipitated as AlN, so that solid solution N can be fixed and reduced. As a cooling rate therefor, it is preferable that the cooling rate to room temperature is 2.0 ° C./second or less after completion of the hot rolling or hot forging. By cooling at this cooling rate, solid solution N is combined with Al during cooling, and precipitated as AlN, so that solid solution N can be reduced. The steel material structure can also be a mixed phase of ferrite grains and pearlite grains more suitable for cutting.

この冷却速度があまり速くなり過ぎると、AlNが析出するための十分な時間を確保することができず、冷却後も固溶Nが多く残存するため、冷間加工性、被削性が劣化する。また、却って、ベイナイトやマルテンサイト等の硬質相の生成割合が増加することによって、鋼材の強度が上昇しすぎて、被削性が低下するので、好ましくは2.0℃/秒以下とする。一方、冷却速度は、遅ければ遅いほど、AlNが生成しやすくなるので、好ましいが、実操業のことを考えると、0.001℃/s以上が好ましい。 If this cooling rate becomes too fast, sufficient time for AlN to precipitate cannot be secured, and a large amount of solid solution N remains after cooling, so that cold workability and machinability deteriorate. . On the other hand, since the strength of the steel material increases excessively and the machinability decreases due to an increase in the generation ratio of hard phases such as bainite and martensite, the temperature is preferably 2.0 ° C./second or less. On the other hand, the slower the cooling rate, the better because AlN is likely to be generated. However, considering the actual operation, 0.001 ° C./s or more is preferable.

摩擦圧接
摩擦圧接自体は常法で良く、公知の条件範囲で良いが、前記した通り、素材低炭素鋼材や、複合鋼化する相手鋼材の組成に応じて、摩擦圧接中に化合物Nを分解して、固溶N量を増加させられるような摩擦熱(摩擦熱量)が得られるような条件にすることが好ましい。この点、素材低炭素鋼材の組成に応じて、摩擦圧力(MPa)、アップセット圧力(接合部への丸棒両端部からの加圧力、MPa)、摩擦時間(sec)、アップセット時間(接合部への加圧時間、sec)、回転数(rpm)などの主要な条件の最適値を、公知の条件範囲から選択する。
Friction welding Friction welding itself may be a conventional method and may be carried out in a known condition range. However, as described above, compound N is decomposed during friction welding according to the composition of the low-carbon steel material or the counterpart steel material to be composite steel. Therefore, it is preferable that the frictional heat (the amount of frictional heat) that can increase the solute N amount is obtained. In this regard, depending on the composition of the low carbon steel material, friction pressure (MPa), upset pressure (pressure applied from both ends of the round bar to the joint, MPa), friction time (sec), upset time (joint The optimum value of main conditions such as pressurization time to the part, sec), and rotation speed (rpm) is selected from a known condition range.

摩擦圧接による複合鋼材化
本発明が対象とする摩擦圧接による複合鋼材は、市販の摩擦圧接機により摩擦圧接が可能であれば、目的とする前記機械構造部品に応じて、本発明の低炭素鋼材に対して、種々の鋼種の相手鋼材が選択できる。また、本発明の低炭素鋼材形状や複合鋼材形状も、目的とする前記機械構造部品に応じて種々の形状が選択できる。例えば、本発明の低炭素鋼材同士を摩擦圧接しても良く、また、相手材をS45CやSCr420Hなどの機械構造用炭素鋼、合金鋼、V添加鋼、B添加鋼などとして、切削性や強度などの種々の特性を基準に選択して組み合わせても良い。また、形状も、摩擦圧接する鋼材同士の形状が異なっていても、同じあるいは類似であっても勿論良く、棒材同士の組み合わせ、頭部(円形材、角形材、傘状材、リング状材など)と軸となる棒材との組み合わせなど、自由に複合材形状が選択できる。
Composite steel material by friction welding The composite steel material by friction welding targeted by the present invention is a low carbon steel material according to the present invention, depending on the intended mechanical structure component, as long as friction welding can be performed by a commercially available friction welding machine. On the other hand, various steel types can be selected. Moreover, the low carbon steel shape and composite steel shape of this invention can also select various shapes according to the said machine structural component made into the objective. For example, the low carbon steel materials of the present invention may be friction welded together, and the mating material may be a carbon steel for mechanical structures such as S45C or SCr420H, alloy steel, V-added steel, B-added steel, etc. These may be selected and combined based on various characteristics. In addition, the shape of the steel materials to be friction welded may be different or the same or similar. Of course, a combination of bars, a head (round material, square material, umbrella material, ring material) Etc.) and a bar material to be used as a shaft.

これら摩擦圧接による複合材は、主として、本発明の機械構造用鋼材側が浸炭、窒化、浸炭窒化などの表面硬化処理を施され、次いで、複合材全体あるいは本発明の機械構造用鋼材側だけが焼戻し処理されて、機械構造部品とされる。なお、機械構造部品としての用途に応じて、公知の防錆処理や防錆被覆などの適当な表面処理が施されても良い。   These composite materials by friction welding are mainly subjected to surface hardening treatment such as carburizing, nitriding, carbonitriding on the machine structural steel side of the present invention, and then tempering the entire composite material or only the mechanical structural steel side of the present invention. Processed into machine structural parts. In addition, according to the use as a machine structural component, suitable surface treatments, such as a well-known antirust process and antirust coating, may be given.

以下、実施例を挙げて、本発明をより具体的に説明するが、本発明はかかる実施例によって限定的に解釈されるものではない。   EXAMPLES Hereinafter, although an Example is given and this invention is demonstrated more concretely, this invention is not limitedly interpreted by this Example.

表1〜4に示す種々の成分組成の低炭素鋼を溶製後に、表5〜8に示す条件で熱間圧延あるいは熱間鍛造して、鋼中の化合物N、固溶N量、更にはMnSのアスペクト比と最大長さとを作り分けた、共通してφ80mmの丸棒(鋼材)を製造した。なお、表1〜4において、各元素が検出されない場合は空欄とし、下向きの矢印は上の欄の含有量と同じであることを示す。   After melting low carbon steel having various composition shown in Tables 1 to 4, hot rolling or hot forging under the conditions shown in Tables 5 to 8, compound N in the steel, amount of solute N, and A round bar (steel material) having a diameter of 80 mm was manufactured in common with the aspect ratio and the maximum length of MnS. In Tables 1 to 4, when each element is not detected, it is blank, and the downward arrow indicates the same content as the upper column.

そして、機械構造部品を模擬して、これら低炭素鋼材を、これら低炭素鋼材同士、および相手材をS45Cの鋼材として、各々摩擦圧接して複合鋼材とした。そして、表9〜12に示す通り、これら複合鋼材の衝撃特性、曲げ疲労特性を各々評価した。ここで、各表では同じ鋼種No.のものが同一の例を示しており、表1、表5、表9の各例が各々対応し、表2、表6、表10の各例が各々対応し、表3、表7、表11の各例が各々対応し、表4、表8、表12の各例が各々対応している。   Then, by simulating machine structural parts, these low carbon steel materials were friction welded to each other with these low carbon steel materials and the counterpart material as steel materials of S45C to obtain composite steel materials. And as shown to Tables 9-12, the impact characteristic and bending fatigue characteristic of these composite steel materials were evaluated, respectively. Here, in each table, the same steel type No. shows the same example, each example in Table 1, Table 5, and Table 9 corresponds to each example, and each example in Table 2, Table 6, and Table 10 respectively. Corresponding, each example of Table 3, Table 7, and Table 11 corresponds, and each example of Table 4, Table 8, and Table 12 corresponds respectively.

低炭素鋼材の製造条件:
具体的には、本発明の鋼材組織を得るために、以下の製造工程を実施した。
溶解・鋳造:供試鋼150kgを真空誘導炉で溶解し、上面:φ245mm×下面:φ210mm×長さ:480mmのインゴットに鋳造した。
ビレット鍛造:前記インゴットを1200℃に加熱して、ビレット(155mm角)に熱間鍛造し、冷却した。
Production conditions for low carbon steel:
Specifically, in order to obtain the steel structure of the present invention, the following manufacturing process was performed.
Melting / casting: 150 kg of the test steel was melted in a vacuum induction furnace and cast into an ingot having an upper surface: φ245 mm × lower surface: φ210 mm × length: 480 mm.
Billet forging: The ingot was heated to 1200 ° C., hot forged into billets (155 mm square), and cooled.

ここで、表のうち、表5、6、7(表1、2、3)の鋼種1A〜2Zの低炭素鋼材は、熱間圧延により、下記の製造条件によって丸棒として製造した。
切断、溶接:この鍛造ビレットの端部を切断し、ダミービレット(155mm角×9〜10m長さ)を溶接した。
熱間圧延:このダミービレット溶接後のビレットを950〜1250℃の範囲で加熱後、750〜1050℃の範囲でΦ80mmの丸棒に熱間圧延し、圧延終了後、0.5〜2.0℃/sの冷却速度範囲で冷却した。
このうち、比較例である1C-5、1C-6、1C-9、1D-5の低炭素鋼材は、ビレット加熱温度、熱間圧延の温度、あるいは圧延終了後の冷却速度を、表5に示す通り、上記各好ましい条件から外して製造した。
Here, among the tables, the low carbon steel materials of steel types 1A to 2Z in Tables 5, 6, and 7 (Tables 1, 2, and 3) were manufactured as round bars by hot rolling under the following manufacturing conditions.
Cutting and welding: The end of this forged billet was cut and a dummy billet (155 mm square × 9 to 10 m long) was welded.
Hot rolling: The billet after the dummy billet welding is heated in the range of 950 to 1250 ° C., then hot-rolled to a Φ80 mm round bar in the range of 750 to 1050 ° C., and after the rolling is completed, 0.5 to 2.0 Cooling was performed at a cooling rate range of ° C / s.
Among these, the low carbon steel materials of 1C-5, 1C-6, 1C-9, and 1D-5, which are comparative examples, show billet heating temperature, hot rolling temperature, or cooling rate after rolling in Table 5. As shown, it was manufactured out of the above preferred conditions.

また、表のうち、表8(表4)の鋼種3A〜3Mの低炭素鋼材は、熱間鍛造により、下記の製造条件によって丸棒として製造した。
熱間鍛造:前記鍛造ビレットを1200℃の範囲で加熱後、900℃でΦ80mmの丸棒に熱間鍛造し、鍛造終了後、1.0℃/sの冷却速度範囲で冷却した。
Moreover, the low carbon steel materials of steel types 3A to 3M in Table 8 (Table 4) in the table were manufactured as round bars by hot forging under the following manufacturing conditions.
Hot forging: The forged billet was heated in the range of 1200 ° C., then hot forged into a round bar of Φ80 mm at 900 ° C., and cooled at a cooling rate range of 1.0 ° C./s after completion of forging.

鋼組織
前記φ80の各丸棒(低炭素鋼材)は、組織観察の結果、発明例と1D-5以外の比較例のいずれも、フェライトとパーライトのみの2相が混在する混相であることを確認した。一方、圧延後の冷却速度が好ましい条件よりも速い1D-5は一部ベイナイトが生成していた。組織観察は、前記各丸棒を長手方向の中心で切断し、切断面(長手方向に対して90°方向の径方向断面)を樹脂に埋め込み、エメリー紙、ダイヤモンドバフで試料表面を鏡面研磨後、表面をナイタールでエッチングした。これを光学顕微鏡を用い、D/4位置を倍率400倍で観察した。
Steel structure As a result of observation of the structure, each round bar (low carbon steel) of φ80 confirms that both the invention example and the comparative example other than 1D-5 are mixed phases in which only two phases of ferrite and pearlite are mixed. did. On the other hand, 1D-5, which has a faster cooling rate after rolling than the preferred conditions, partially produced bainite. For tissue observation, each round bar is cut at the center in the longitudinal direction, and the cut surface (radial cross section at 90 ° to the longitudinal direction) is embedded in resin, and the sample surface is mirror-polished with emery paper or diamond buff. The surface was etched with nital. This was observed using an optical microscope at a D / 4 position at a magnification of 400 times.

MnSの形状(アスペクト比、数)測定方法
前記φ80の各丸棒サンプルを圧延あるいは鍛造方向中心で切断し、樹脂に埋め込み、エメリー紙、ダイヤモンドバフで試料表面を鏡面研磨した。この研磨試料表面をナイタールでエッチング後、光学顕微鏡を用い、D/4 位置を倍率400 倍で観察し、5箇所写真撮影した。そして、最大長さが2μm 以上のMnS(硫化物系介在物)の個数を数えて5箇所の平均値を求め、このMnSの平均個数とした。また、これら最大長さが2μm 以上のMnSのアスペクト比を各々測定し、その平均値を、その鋼材におけるMnSのアスペクト比とした。なお、前記光学顕微鏡で観察される介在物のMnSか否かの確認、同定はX 線分光装置(EDX) により識別した。
Method for measuring shape (aspect ratio, number) of MnS Each round bar sample of φ80 was cut at the center of the rolling or forging direction, embedded in resin, and the sample surface was mirror-polished with emery paper or diamond buff. After this polished sample surface was etched with nital, the D / 4 position was observed at 400 times magnification using an optical microscope, and five photographs were taken. Then, the number of MnS (sulfide inclusions) having a maximum length of 2 μm or more was counted to obtain an average value at five locations, which was used as the average number of MnS. Further, the aspect ratios of MnS having a maximum length of 2 μm or more were measured, and the average value was taken as the aspect ratio of MnS in the steel material. Confirmation and identification of whether or not the inclusion was MnS observed with the optical microscope was identified by an X-ray spectrometer (EDX).

鋼材の被削性測定方法
被削性は、前記φ80の各丸棒の旋削試験によって評価した。試験機として、NC旋盤を用い、被削性評価用試験片(φ80×350mmL)を旋盤加工した。この時用いた工具の逃げ面における工具摩耗量(Vb)の経時変化を測定し、以下の条件で3000m 削った後のVbを測定した。切削試験条件は以下のとおりである。
工具:TiAlN コーティングチップ
切削速度:200m/minで、周速一定
切削油:無し(乾式)
切り込み量:1.5mm
送り量:0.25mm/rev
そして、3000m 切削後のVb摩耗量が60μm 以下の鋼材を、被削性に優れるとして合格判定した。
Method for measuring machinability of steel material The machinability was evaluated by a turning test of each round bar of φ80. An NC lathe was used as a testing machine, and a machinability evaluation test piece (φ80 × 350 mmL) was turned. The change over time in the amount of tool wear (Vb) on the flank of the tool used at this time was measured, and Vb after 3000 m of cutting was measured under the following conditions. The cutting test conditions are as follows.
Tool: TiAlN coated chip Cutting speed: 200m / min, constant peripheral cutting oil: None (dry type)
Cutting depth: 1.5mm
Feed amount: 0.25mm / rev
Then, a steel material having a Vb wear amount of 60 μm or less after cutting 3000 m was judged to be acceptable as having excellent machinability.

冷鍛性評価方法
冷鍛性は、前記φ80の各丸棒の端面拘束圧縮試験によって評価した。試験機として、1600トンプレスを用い、冷鍛性評価用試験片(φ10×15mmL )を圧縮加工した。試験片は、圧延材のD/4 位置(D:直径)から切り出した。室温、ひずみ速度10/sで80%の圧縮加工を行った。圧縮後の試験片表面を倍率20倍の実体顕微鏡で観察し、割れの有無を確認した。割れのない鋼材を冷鍛性に優れるとして、合格判定した。
Cold forgeability evaluation method Cold forgeability was evaluated by the end face constrained compression test of each round bar of φ80. A 1600-ton press was used as a testing machine, and a test piece for cold forgeability evaluation (φ10 × 15 mmL) was compressed. The test piece was cut out from the D / 4 position (D: diameter) of the rolled material. 80% compression processing was performed at room temperature and a strain rate of 10 / s. The surface of the test specimen after compression was observed with a stereomicroscope at a magnification of 20 times to confirm the presence or absence of cracks. It was determined that the steel material without cracks was excellent in cold forgeability.

摩擦圧接試験
前記φ80の各丸棒の圧延あるいは鍛造方向に沿って、D/4位置からφ20mm×100mmLの棒材(試験片)を切出した。自動摩擦圧接機として日東制機(株)製の製品名FF−4511−Cを用い、ブレーキ法によって摩擦圧接した。即ち、前記切出した棒材同士(供試材同士の摩擦圧接鋼材)、および前記切出した棒材の相手材をS45Cの鋼材として(S45Cとの摩擦圧接鋼材)として、各々長手方向に端部同士を突き合わせた丸棒複合鋼材(鋼部品)として、各々摩擦圧接した。
Friction welding test A rod (test piece) of φ20 mm × 100 mmL was cut out from the D / 4 position along the rolling or forging direction of each φ80 round bar. A product name FF-4511-C manufactured by Nitto Seiki Co., Ltd. was used as an automatic friction welding machine, and friction welding was performed by a brake method. That is, the cut bar materials (friction welded steel materials of the test materials) and the cut bar material as the steel material of S45C (friction pressure welded steel material with S45C), each end in the longitudinal direction. As a round bar composite steel material (steel part), the friction welding was performed.

摩擦圧接は、各例とも共通して以下の条件に従って行った。
摩擦圧力:100MPa
アップセット圧力(接合部への丸棒両端部からの加圧力):180MPa、
摩擦時間:10sec、
アップセット時間(接合部への加圧時間):10sec、
回転数:1600rpm、
全寄りしろ:8〜15mm(当初の丸棒長さからの縮み量)
Friction welding was performed in accordance with the following conditions in common with each example.
Friction pressure: 100 MPa
Upset pressure (pressure applied from both ends of the round bar to the joint): 180 MPa,
Friction time: 10 sec,
Upset time (pressurization time to the joint): 10 sec,
Rotation speed: 1600 rpm,
Total margin: 8-15mm (shrinkage from the original round bar length)

摩擦圧接部品のMnSの形状(アスペクト比、数)測定方法
前記摩擦圧接によって形成された接合部から1mm幅の範囲の前記低炭素鋼材側の熱影響部の鋼中における、アスペクト比が2以下で、且つ、最大長さが1μm以下のMnSの個数を測定した。前記1mm幅の範囲内の前記低炭素鋼材側の熱影響部を任意の5箇所切断して、前記低炭素鋼材と同じ条件で処理して、光学顕微鏡を用い、D/4 位置を倍率400 倍で観察し、写真撮影した。そして、アスペクト比が2以下で、且つ、最大長さが1μm以下のMnSの個数を数えて5箇所の平均値を求めた。なお、前記光学顕微鏡で観察される介在物のMnSか否かの確認、同定はX 線分光装置(EDX) により識別した。
Method for measuring shape (aspect ratio, number) of MnS of friction welded part In the steel in the heat affected zone on the low carbon steel material side in the range of 1 mm width from the joint formed by the friction welding, the aspect ratio is 2 or less The number of MnS having a maximum length of 1 μm or less was measured. The heat affected zone on the low carbon steel material side within the 1 mm width range is cut at any five locations, treated under the same conditions as the low carbon steel material, and the D / 4 position is 400 times magnification using an optical microscope. Observed and photographed. Then, the number of MnS having an aspect ratio of 2 or less and a maximum length of 1 μm or less was counted to obtain an average value at 5 locations. Confirmation and identification of whether or not the inclusion was MnS observed with the optical microscope was identified by an X-ray spectrometer (EDX).

衝撃特性評価
Φ20mm×約200mmLの前記供試材同士の摩擦圧接鋼材およびS45Cとの摩擦圧接鋼材(丸棒複合鋼材)の中央位置から、接合部分がノッチ底となるように、1辺が10mmの正方形断面×55mmLのシャルピー試験片を作製した。なお、ノッチ形状は、R10(mm)とした。ノッチ導入面以外の3面にCuめっきを施した(TP加工)。そして、この作製試験片を930℃浸炭−油焼入れ(浸炭処理)した後、170℃で焼戻し処理を施した。
Impact characteristics evaluation From the center position of the friction welding steel material (round bar composite steel material) of the friction test welding steel material and S45C between the test materials of Φ20 mm × about 200 mmL, one side is 10 mm so that the joint portion becomes a notch bottom. A Charpy test piece having a square cross section x 55 mmL was prepared. The notch shape was R10 (mm). Cu plating was performed on three surfaces other than the notch introduction surface (TP processing). And after making this preparation test piece 930 degreeC carburizing-oil quenching (carburizing process), the tempering process was performed at 170 degreeC.

次いで、シャルピー衝撃試験機にて、前記焼戻し処理後の試験片の衝撃特性評価を行った。試験条件は、室温、負荷速度5m/sの条件で、5回シャルピー衝撃試験を行い、シャルピー衝撃値(吸収エネルギー)を測定した。そして、全ての接合部品で、吸収エネルギーが10J(ジュール)以上となる複合鋼材を合格とした。表9〜表12に記載したシャルピー値は、全て、この吸収エネルギーの値(単位:J)を示す。   Subsequently, the impact property evaluation of the test piece after the tempering treatment was performed with a Charpy impact tester. The test conditions were room temperature and a load speed of 5 m / s. The Charpy impact test was performed five times and the Charpy impact value (absorbed energy) was measured. And in all joining components, the composite steel material from which absorbed energy became 10J (joule) or more was set as the pass. All Charpy values listed in Tables 9 to 12 indicate the value of the absorbed energy (unit: J).

疲労特性評価
Φ20mm×約200mmLの前記供試材同士の摩擦圧接鋼材およびS45Cとの摩擦圧接鋼材(丸棒複合鋼材)の中央位置から、接合部分がノッチ底となるように、1辺が13mmの正方形断面×100mmLの4点曲げ疲労試験片を作製した。なお、ノッチ形状は、R1.5(mm)とした。ノッチ導入面以外の3面にCuめっきを施した(TP加工)。そして、この作製試験片を930℃浸炭−油焼入れ(浸炭処理)した後、170℃で焼戻し処理を施した。
次いで、4点曲げ疲労試験機にて、前記試験片の疲労特性評価を行った。試験条件は、周波数20Hzで荷重4000N(応力609MPa)〜14000(応力2132MPa)の間で荷重を変化させた11水準で行い、2万回寿命に相当する応力(MPa)を求め、これを疲労強度の指標とした。本実施例では、疲労限応力が1000MPa以上となる試験片(複合鋼材)を合格とした。表9〜表12に記載した2万回寿命は、全て、この疲労限応力(単位:MPa)を示す。
Fatigue property evaluation From the center position of the friction welding steel material (round bar composite steel material) with the friction welding steel material of S20C and the above-mentioned test materials of Φ20 mm × about 200 mmL, one side is 13 mm so that the joint portion becomes a notch bottom. A four-point bending fatigue test piece with a square cross section × 100 mmL was prepared. The notch shape was R1.5 (mm). Cu plating was performed on three surfaces other than the notch introduction surface (TP processing). And after making this preparation test piece 930 degreeC carburizing-oil quenching (carburizing process), the tempering process was performed at 170 degreeC.
Next, the fatigue characteristics of the test piece were evaluated with a 4-point bending fatigue tester. The test conditions were performed at 11 levels with a load of 4000 N (stress 609 MPa) to 14000 (stress 2132 MPa) at a frequency of 20 Hz, and a stress (MPa) corresponding to a life of 20,000 times was obtained. It was used as an index. In this example, a test piece (composite steel material) having a fatigue limit stress of 1000 MPa or more was accepted. All the 20,000 times life described in Tables 9 to 12 show this fatigue limit stress (unit: MPa).

表1から表12における、1A〜1Z、2A〜2J、3A〜3Mまでの発明例(但し、1C-5、1C-6、1C-9、1D-5は比較例であり除く)は、鋼成分組成や、鋼中の化合物Nの含有量、固溶N量で、かつ、最大長さが2μm以上のMnSの個数と平均アスペクト比が2以上で、本発明で規定する条件を満足する。   In Tables 1 to 12, invention examples 1A to 1Z, 2A to 2J, 3A to 3M (however, 1C-5, 1C-6, 1C-9, 1D-5 are comparative examples) are steel. The component composition, the content of compound N in steel, the amount of solute N, the number of MnS having a maximum length of 2 μm or more and the average aspect ratio of 2 or more satisfy the conditions specified in the present invention.

この結果、低炭素鋼材として、冷間鍛造などの冷間加工性や被削性が優れている。そして、前記摩擦圧接された摩擦圧接部品(複合鋼)としても、自動車のエンジン部品用途などとして、その接合強度が問われる(要求される)、衝撃特性、曲げ疲労特性が優れている。   As a result, as a low carbon steel material, cold workability such as cold forging and machinability are excellent. Also, the friction welded parts (composite steel) subjected to the friction welding are excellent in impact characteristics and bending fatigue characteristics in which the joining strength is required (required) for automotive engine parts.

これに対して、表1から表12における、1C-5、1C-6、1C-9、1D-5および2K〜2Zまでの比較例は、主要な元素の含有量が上下限を外れるか、鋼成分組成が本発明条件を満足するものの、製造条件が前記した好ましい範囲を外れる。この結果、これら比較例は、低炭素鋼材として、冷間鍛造などの冷間加工性や被削性が劣るか、前記摩擦圧接された摩擦圧接部品(複合鋼)としても、自動車のエンジン部品用途などとして、その接合強度が問われる(要求される)、衝撃特性、曲げ疲労特性が、前記発明例に比して、表9、表11の通り著しく劣っている。   On the other hand, in the comparative examples from 1C-5 to 1C-5, 1C-6, 1C-9, 1D-5 and 2K to 2Z in Tables 1 to 12, whether the content of the main elements deviates from the upper and lower limits, Although the steel component composition satisfies the conditions of the present invention, the production conditions deviate from the preferred range described above. As a result, these comparative examples are low carbon steel materials, which are inferior in cold workability and machinability such as cold forging, or as friction welded parts (composite steel) that are friction welded, such as automotive engine parts. For example, the joint strength is required (required), and the impact characteristics and bending fatigue characteristics are significantly inferior as shown in Tables 9 and 11 as compared with the above-described invention examples.

表5に示す通り、比較例である1C-5、1C-6、1C-9、1D-5の低炭素鋼材は、ビレット加熱温度、熱間圧延の温度、あるいは圧延終了後の冷却速度を、上記各好ましい条件から外れて製造されている。
鋼種1C-5はビレット加熱温度が高すぎる。
鋼種1C-6は圧延温度が高すぎる。
鋼種1C-9は圧延温度が低すぎる。
鋼種1D-5は圧延終了後の冷却速度が速すぎる。
As shown in Table 5, the low carbon steel materials of 1C-5, 1C-6, 1C-9, and 1D-5, which are comparative examples, have a billet heating temperature, a hot rolling temperature, or a cooling rate after completion of rolling. Manufactured outside the above preferred conditions.
Steel type 1C-5 has a billet heating temperature too high.
Steel type 1C-6 has a too high rolling temperature.
Steel type 1C-9 has too low rolling temperature.
In steel type 1D-5, the cooling rate after the end of rolling is too fast.

表1に示す通り、比較例である2K〜2Zの低炭素鋼材は、製法は好ましい条件範囲内であるが、主要な元素の含有量が上下限を外れている。
鋼種2K、2LはC含有量が上下限を各々外れている。
鋼種2M、2NはSi含有量が上下限を各々外れている。
鋼種2O、2PはMn含有量が上下限を各々外れている。
鋼種2QはP含有量が上限を外れている。
鋼種2R、2SはS含有量が上限を外れている。
鋼種2T、2UはCr含有量が上下限を各々外れている。
鋼種2V、2WはAl含有量が上下限を各々外れている。
鋼種2Xは化合物N含有量が下限を外れている。
鋼種2Yは全N含有量と固溶N量が上限を外れている。
鋼種2ZはP含有量が上限を外れている。
As shown in Table 1, the low carbon steel materials of 2K to 2Z, which are comparative examples, have a manufacturing method within a preferable condition range, but the content of main elements is out of the upper and lower limits.
In steel types 2K and 2L, the C content deviates from the upper and lower limits.
In steel types 2M and 2N, the Si content deviates from the upper and lower limits.
In steel types 2O and 2P, the Mn content deviates from the upper and lower limits.
In steel type 2Q, the P content is outside the upper limit.
In steel types 2R and 2S, the S content is outside the upper limit.
In the steel types 2T and 2U, the Cr content deviates from the upper and lower limits.
In steel types 2V and 2W, the Al content deviates from the upper and lower limits.
Steel type 2X has a compound N content outside the lower limit.
In the steel type 2Y, the total N content and the solute N amount are out of the upper limit.
Steel content 2Z has a P content outside the upper limit.

したがって、以上の実施例の結果から、本発明における鋼材の成分組成や組織、製法の、前記摩擦圧接された複合材として要求される衝撃特性、曲げ疲労特性を得るための臨界的な意義乃至効果が裏付けられる。   Therefore, from the results of the above examples, the critical significance or effect for obtaining the impact characteristics and bending fatigue characteristics required for the friction-welded composite of the composition, structure, and manufacturing method of the steel material according to the present invention. Is supported.

本発明によれば、疲労強度、衝撃強度などの部品特性を向上させた、摩擦圧接に適した機械構造用の低炭素鋼材および摩擦圧接部品を提供できる。このため、自動車のエンジン、変速機、差動機などに用いられる減速ギア、デフギアなど歯車、CVTプーリーなどの、摩擦圧接された機械構造部品として、好適に用いることができる。   According to the present invention, it is possible to provide a low carbon steel material and a friction welded part for machine structure suitable for friction welding, which have improved part characteristics such as fatigue strength and impact strength. For this reason, it can be suitably used as a mechanical structure part that is friction-welded, such as a reduction gear, a gear such as a differential gear, and a CVT pulley, which are used in automobile engines, transmissions, and differentials.

Claims (6)

質量%で、C:0.08〜0.61%、Si:0.08〜0.5%、Mn:0.4〜1.5%、P:0.03%以下(但し0%を含まない)、S:0.005〜0.1%、Cr:0.4〜2%、Al:0.005〜0.1%、N:0.02%以下(但し0%を含まない)を各々含み、残部Feおよび不可避的不純物からなるとともに、鋼中の化合物Nの含有量が0.006〜0.02%で、且つ、固溶N量が0.0015%以下(但し0%を含む)であり、最大長さが2μm以上のMnSが鋼中に1mm2 当たり100〜4000個存在し、これらMnSの平均アスペクト比が2以上であることを特徴とする摩擦圧接に適した機械構造用鋼材。 In mass%, C: 0.08 to 0.61%, Si: 0.08 to 0.5%, Mn: 0.4 to 1.5%, P: 0.03% or less (excluding 0%) S): 0.005 to 0.1%, Cr: 0.4 to 2%, Al: 0.005 to 0.1%, N: 0.02% or less (however, not including 0%) Each of them includes the balance Fe and inevitable impurities, the content of compound N in the steel is 0.006 to 0.02%, and the amount of solid solution N is 0.0015% or less (however, 0% is included) ), And MnS having a maximum length of 2 μm or more is present in steel in an amount of 100 to 4000 per mm 2 , and the average aspect ratio of these MnS is 2 or more. Steel material. 前記機械構造用鋼が、更に、質量%で、Ti:0.2%以下(但し0%を含まない)、Nb:0.2%以下(但し0%を含まない)、V:0.2%以下(但し0%を含まない)、B:0.01%以下(但し0%を含まない)、Mo:1%以下(但し0%を含まない)、Cu:1%以下(但し0%を含まない)、Ni:1%以下(但し0%を含まない)の1種又は2種以上を含有する請求項1に記載の摩擦圧接に適した機械構造用鋼材。   Further, the steel for machine structural use in terms of mass%, Ti: 0.2% or less (excluding 0%), Nb: 0.2% or less (excluding 0%), V: 0.2 % Or less (excluding 0%), B: 0.01% or less (excluding 0%), Mo: 1% or less (excluding 0%), Cu: 1% or less (excluding 0%) 2), Ni: 1% or less (excluding 0%), or one or more of them, containing the steel material for mechanical structure suitable for friction welding according to claim 1. 前記機械構造用鋼が、更に、質量%で、Ca:0.02%以下(但し0%を含まない)、REM:0.02%以下(但し0%を含まない)、Li:0.005%以下(但し0%を含まない)、Mg:0.005%以下(但し0%を含まない)の1種又は2種以上を含有する請求項1または2に記載の摩擦圧接に適した機械構造用鋼材。   Further, the steel for machine structural use is, in mass%, Ca: 0.02% or less (excluding 0%), REM: 0.02% or less (excluding 0%), Li: 0.005 % Or less (however, not including 0%), Mg: 0.005% or less (however, not including 0%) one or more kinds of machines suitable for friction welding according to claim 1 or 2 Structural steel. 質量%で、C:0.08〜0.61%、Si:0.08〜0.5%、Mn:0.4〜1.5%、P:0.03%以下(但し0%を含まない)、S:0.005〜0.1%、Cr:0.4〜2%、Al:0.005〜0.1%、N:0.02%以下(但し0%を含まない)を各々含み、残部Feおよび不可避的不純物からなるとともに、鋼中の化合物Nの含有量が0.006〜0.02%で、且つ、固溶N量が0.0015%以下(但し0%を含む)であり、最大長さが2μm以上のMnSが鋼中に1mm2 当たり100〜4000個存在し、これらMnSの平均アスペクト比が2以上である機械構造用鋼材と、他の炭素鋼材あるいは合金鋼材とが、摩擦圧接によって接合されて所望の形状の複合鋼とされ、更に、表面硬化処理および焼戻し処理が施されてなる摩擦圧接部品であって、前記摩擦圧接によって形成された接合部から1mm幅の範囲の前記機械構造用鋼材側の熱影響部の鋼中における、アスペクト比が2以下で、且つ、最大長さが1μm以下のMnSを、1mm2 当たり25個以下(但し0個を含む)に規制したことを特徴とする、衝撃特性、曲げ疲労特性に優れた摩擦圧接部品。 In mass%, C: 0.08 to 0.61%, Si: 0.08 to 0.5%, Mn: 0.4 to 1.5%, P: 0.03% or less (excluding 0%) S): 0.005 to 0.1%, Cr: 0.4 to 2%, Al: 0.005 to 0.1%, N: 0.02% or less (however, not including 0%) Each of them includes the balance Fe and inevitable impurities, the content of compound N in the steel is 0.006 to 0.02%, and the amount of solid solution N is 0.0015% or less (however, 0% is included) ), And a steel material for machine structural use in which MnS having a maximum length of 2 μm or more is present in steel in an amount of 100 to 4000 per mm 2 , and the average aspect ratio of these MnS is 2 or more, and other carbon steel materials or alloy steel materials Are joined by friction welding to form a composite steel of a desired shape, and further, surface hardening treatment and tempering treatment The aspect ratio in the steel of the heat affected zone on the machine structural steel side in the range of 1 mm width from the joint formed by the friction welding is 2 or less, and A friction welding part excellent in impact characteristics and bending fatigue characteristics, characterized in that MnS having a maximum length of 1 μm or less is regulated to 25 or less (including 0) per 1 mm 2 . 前記機械構造用鋼が、更に、質量%で、Ti:0.2%以下(但し0%を含まない)、Nb:0.2%以下(但し0%を含まない)、V:0.2%以下(但し0%を含まない)、B:0.01%以下(但し0%を含まない)、Mo:1%以下(但し0%を含まない)、Cu:1%以下(但し0%を含まない)、Ni:1%以下(但し0%を含まない)の1種又は2種以上を含有する請求項4に記載の衝撃特性、曲げ疲労特性に優れた摩擦圧接部品。   Further, the steel for machine structural use in terms of mass%, Ti: 0.2% or less (excluding 0%), Nb: 0.2% or less (excluding 0%), V: 0.2 % Or less (excluding 0%), B: 0.01% or less (excluding 0%), Mo: 1% or less (excluding 0%), Cu: 1% or less (excluding 0%) 5), Ni: 1% or less (excluding 0%), or one or more of them, the friction welded part having excellent impact characteristics and bending fatigue characteristics according to claim 4. 前記機械構造用鋼が、更に、質量%で、Ca:0.02%以下(但し0%を含まない)、REM:0.02%以下(但し0%を含まない)、Li:0.005%以下(但し0%を含まない)、Mg:0.005%以下(但し0%を含まない)の1種又は2種以上を含有する請求項4または5に記載の衝撃特性、曲げ疲労特性に優れた摩擦圧接部品。   Further, the steel for machine structural use is, in mass%, Ca: 0.02% or less (excluding 0%), REM: 0.02% or less (excluding 0%), Li: 0.005 % Or less (however, not including 0%), Mg: not more than 0.005% (however, not including 0%), or two or more kinds of impact properties and bending fatigue properties according to claim 5 Excellent friction welding parts.
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WO2013146880A1 (en) * 2012-03-30 2013-10-03 愛知製鋼株式会社 Steel material for friction welding, and method for producing same
JP2014177668A (en) * 2013-03-14 2014-09-25 Honda Motor Co Ltd Pulley for belt type cvt and steel for pully
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JP2018150582A (en) * 2017-03-13 2018-09-27 新日鐵住金株式会社 Forging component
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JP7376784B2 (en) 2019-12-13 2023-11-09 日本製鉄株式会社 hot forged parts
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JP2014177668A (en) * 2013-03-14 2014-09-25 Honda Motor Co Ltd Pulley for belt type cvt and steel for pully
JP2017066475A (en) * 2015-09-30 2017-04-06 新日鐵住金株式会社 Hot forging component and manufacturing method of hot forging component
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JP2018016866A (en) * 2016-07-29 2018-02-01 国立大学法人大阪大学 Steel for friction stirring jointing and friction stirring jointing method
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CN106493467A (en) * 2016-12-26 2017-03-15 重庆派馨特机电有限公司 A kind of stirring-head thermal fatigue resistance material
JP2018150582A (en) * 2017-03-13 2018-09-27 新日鐵住金株式会社 Forging component
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JP7376784B2 (en) 2019-12-13 2023-11-09 日本製鉄株式会社 hot forged parts
JP7485946B2 (en) 2020-09-14 2024-05-17 日本製鉄株式会社 Joint, automobile part, and method for manufacturing joint
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