JP2022000540A - Carburization method of steel part and manufacturing method of steel part - Google Patents

Carburization method of steel part and manufacturing method of steel part Download PDF

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JP2022000540A
JP2022000540A JP2021134799A JP2021134799A JP2022000540A JP 2022000540 A JP2022000540 A JP 2022000540A JP 2021134799 A JP2021134799 A JP 2021134799A JP 2021134799 A JP2021134799 A JP 2021134799A JP 2022000540 A JP2022000540 A JP 2022000540A
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carburizing
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steel
steel part
sodium silicate
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祐司 宮本
Yuji Miyamoto
秀幸 飛鷹
Hideyuki Tobitaka
冕 張
Mian Zhang
節雄 高木
Setsuo Takagi
広郁 宮原
Hirofumi Miyahara
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NSK Ltd
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Abstract

To provide a carburization method of a steel part capable of obtaining a deep carburization depth in a short time, and a manufacturing method of the steel part.SOLUTION: A carburization agent in which an Fe-C alloy in a power state and a binder composed of a sodium silicate aqueous solution for binding the Fe-C alloy in a powder state together are mixed is caused to contact with at least a part of a surface of a steel part, and the steel part is kept for certain period of time at a temperature range of an austenite range that is higher than an eutectic point of a raw material and less than a peritectic point to form a carburization layer with a carburization depth of 1.9 mm or more.SELECTED DRAWING: Figure 1

Description

本発明は、鋼製部品の浸炭方法及び鋼製部品の製造方法に関する。 The present invention relates to a method for carburizing steel parts and a method for manufacturing steel parts.

一般に、歯車、軸受等の機械部品においては、表面近傍(例えば表面から1mm程度の深さ)の硬度を高くして、耐摩耗性、摺動性、疲労強度等の諸特性を向上させるために、
浸炭焼き入れを施すことがある。このような浸炭法は、固体浸炭、液体浸炭、ガス浸炭、
真空浸炭に分類され、いずれもオーステナイト域に加熱した部品表面から炭素(C)を侵入させる処理である。工業的には、大部分がガス浸炭であり、Fe−C平衡状態図におけるA1点以上の温度に加熱した炉内に、キャリアガスとして吸熱型変成ガスを流し、更に、エンリッチガスとしてプロパン、ブタン等の炭化水素ガスを供給する。必要とされる浸炭深さは、部品のサイズ、摩耗量や疲労特性、使用する鋼材の化学成分、製品の使用条件等に応じて決定されるため、部品毎に所望の深さとなる浸炭時間で処理される。
Generally, in mechanical parts such as gears and bearings, in order to increase the hardness near the surface (for example, at a depth of about 1 mm from the surface) to improve various characteristics such as wear resistance, slidability, and fatigue strength. ,
May be charcoal-burned. Such carburizing methods include solid carburizing, liquid carburizing, gas carburizing,
It is classified as vacuum carburizing, and all of them are treatments in which carbon (C) is invaded from the surface of a heated component in the austenite region. Industrially, most of them are gas hydrocarbons, and a heat-absorbing modified gas is flowed as a carrier gas in a furnace heated to a temperature of point A1 or higher in the Fe-C equilibrium diagram, and propane and butane are further enriched. Etc. to supply hydrocarbon gas. The required carburizing depth is determined according to the size of the part, wear amount and fatigue characteristics, chemical composition of the steel material used, usage conditions of the product, etc., so the carburizing time is the desired depth for each part. It is processed.

一方、転がり軸受の場合、荷重を受けて回転すると、内輪・外輪の軌道面および転動体の転動面は絶えず繰り返し荷重を受けるので、材料の疲れによって、フレーキングと呼ばれるうろこ状のはくり損傷が生じる。大きな荷重下で転動疲労強度を確保するため、それぞれの部材表面から例えば10mmを超える浸炭深さが必要とされるなど、荷重が負荷される領域が広範囲に及ぶことがある(図4参照)。しかし、この部品を950℃でガス浸炭処理する場合、200〜300時間もの処理時間が必要となる。そのため、浸炭処理では、リードタイムの過大が最大の生産課題となっており、浸炭処理時間の短縮を求めて各種検討がなされている(特許文献1〜3参照)。 On the other hand, in the case of rolling bearings, when they rotate under a load, the raceway surfaces of the inner and outer rings and the rolling surface of the rolling element are constantly repeatedly loaded, and the material fatigue causes scaly peeling damage called flaking. Occurs. In order to secure rolling fatigue strength under a large load, the area to which the load is applied may be wide, for example, a carburizing depth of more than 10 mm is required from the surface of each member (see FIG. 4). .. However, when this part is carburized by gas at 950 ° C., a processing time of 200 to 300 hours is required. Therefore, in the carburizing treatment, an excessive lead time is the biggest production issue, and various studies have been made in order to shorten the carburizing treatment time (see Patent Documents 1 to 3).

特許文献1には、高周波加熱を用いて、共晶点以上、包晶点以下の温度に加熱したワークに、浸炭源として炭化水素ガスを供給して浸炭処理する手法が記載されている。しかし、共晶点以上の温度域では、オーステナイトの固溶限を超えて炭素が侵入すると、ワーク表面に液相が生成される。液相は重力によって容易に移動するため、ワーク形状を保持し続けるには限界がある。また、炭化水素ガスを浸炭源として、ワーク表面に炭素を均一に吸着させることは難しく、炭素の流入量を固溶限以下に制御することは困難である。 Patent Document 1 describes a method of carburizing a work heated to a temperature above the eutectic point and below the peritectic point by supplying a hydrocarbon gas as a carburizing source by using high frequency heating. However, in the temperature range above the eutectic point, when carbon invades beyond the solid solution limit of austenite, a liquid phase is formed on the work surface. Since the liquid phase moves easily due to gravity, there is a limit to maintaining the shape of the work. Further, it is difficult to uniformly adsorb carbon on the work surface using a hydrocarbon gas as a carburizing source, and it is difficult to control the amount of carbon inflow below the solid solution limit.

引用文献2には、ワークの表面に炭素をコーティングし、所定の温度に加熱し、炭素を内部に拡散する手法が記載されている。しかしながら、この手法により得られる硬化層は、ごく表面のみであり、短い浸炭時間で、転がり軸受に必要な広範囲でかつ十分な浸炭深さを得るためには、十分な量の炭素源を供給する必要がある。また、引用文献2は、共晶点以下の浸炭を想定しており、共晶点以上の温度域に適用すると、炭素と接触したワーク表面において液相が生じるため、炭素流入量を固溶限以下に制御することは難しい。 Reference 2 describes a method in which the surface of a work is coated with carbon, heated to a predetermined temperature, and the carbon is diffused inside. However, the hardened layer obtained by this method is only the surface, and supplies a sufficient amount of carbon source to obtain the wide range and sufficient carburizing depth required for rolling bearings in a short carburizing time. There is a need. Further, Cited Document 2 assumes carburization below the eutectic point, and when applied to a temperature range above the eutectic point, a liquid phase is generated on the work surface in contact with carbon, so that the amount of carbon inflow is limited to a solid solution. It is difficult to control below.

引用文献3には、FeとCの化合物である鉄炭化物を浸炭源に用いる浸炭手法が記載されている。炭素は、オーステナイトと平衡する鉄炭化物から供給される。また、鉄粉末とGr(グラファイト)粉末と鉄合金粉末をメカニカルミリングにより鉄炭化物を生成させ、浸炭源剤を製造することが記載されている。しかし、引用文献3も共晶点以下の浸炭を想定しており、上記したように、共晶点以上の温度域に適用すると、炭素と接触したワーク表面において液相が生じるため、炭素流入量を固溶限以下に制御することは難しい。 Cited Document 3 describes a carburizing method using iron carbide, which is a compound of Fe and C, as a carburizing source. Carbon is supplied from iron carbides that are in equilibrium with austenite. Further, it is described that iron carbide is produced by mechanical milling of iron powder, Gr (graphite) powder and iron alloy powder to produce a carburizing source agent. However, Cited Document 3 also assumes carburization below the eutectic point, and as described above, when applied to a temperature range above the eutectic point, a liquid phase is generated on the work surface in contact with carbon, so the amount of carbon inflow. Is difficult to control below the solid solution limit.

特許第3899081号公報Japanese Patent No. 3899081 特開2015−108164号公報Japanese Unexamined Patent Publication No. 2015-108164 特開2010−1508号公報Japanese Unexamined Patent Publication No. 2010-1508

本発明は上記事項に鑑みてなされたものであり、その目的は、短い浸炭時間で、広範囲でかつ十分な浸炭深さを得られる鋼材部品の浸炭方法及び鋼製部品の製造方法を提供することにある。 The present invention has been made in view of the above matters, and an object of the present invention is to provide a method for carburizing steel parts and a method for manufacturing steel parts, which can obtain a wide range and sufficient carburizing depth in a short carburizing time. It is in.

本発明は下記構成からなる。
(1) 粉末状のFe−C合金と、前記粉末状のFe−C合金の粉末同士を結着させる珪酸ナトリウム水溶液から成る結着剤とを混練した浸炭剤を、鋼製部品の少なくとも一部の表面に接触させ、前記鋼製部品を素材の共晶点以上、包晶点未満のオーステナイト域の温度範囲に一定時間保持し、少なくとも1.9mm以上の浸炭深さの浸炭層を形成する、鋼製部品の浸炭方法。
(2) 浸炭層を備える鋼製部品の製造方法であって、
粉末状のFe−C合金と、珪酸ナトリウム水溶液から成る結着剤とを混練した浸炭剤を鋼製部品の少なくとも一部の表面に接触させ、前記鋼製部品を素材の共晶点以上、包晶点未満のオーステナイト域の温度範囲に一定時間保持し、少なくとも1.9mm以上の浸炭深さの前記浸炭層を形成する、鋼製部品の製造方法。
The present invention has the following configuration.
(1) A carburizing agent obtained by kneading a powdery Fe-C alloy and a binder composed of an aqueous sodium silicate that binds the powdered Fe-C alloy powder to each other is used as a carburizing agent for at least a part of steel parts. The steel part is kept in the temperature range of the austenite region above the eutectic point and below the peritectic point for a certain period of time to form a carburized layer with a carburizing depth of at least 1.9 mm or more. Carburizing method for steel parts.
(2) A method for manufacturing steel parts having a carburized layer.
A carburizing agent obtained by kneading a powdery Fe-C alloy and a binder composed of an aqueous solution of sodium silicate is brought into contact with the surface of at least a part of the steel parts, and the steel parts are packaged at or above the eutectic point of the material. A method for manufacturing a steel part, which is maintained in a temperature range in the austenite region below the crystal point for a certain period of time to form the carburized layer having a carburized depth of at least 1.9 mm or more.

本発明によれば、短い浸炭時間で、広範囲でかつ十分な浸炭深さを有する鋼製部品を得ることができる。 According to the present invention, it is possible to obtain a steel part having a wide range and a sufficient carburizing depth in a short carburizing time.

Fe−C平衡状態図である。It is a Fe-C equilibrium state diagram. 固相のFe−C合金粉末と、結着剤としての珪酸ナトリウム水溶液とが混合状態の浸炭剤がワーク表面に接触した状態を示す概念図である。FIG. 5 is a conceptual diagram showing a state in which a carburizing agent in a mixed state of a solid-phase Fe—C alloy powder and an aqueous sodium silicate solution as a binder is in contact with the work surface. 図2に示す状態から更に加熱して浸炭が開始された状態を示す概念図である。It is a conceptual diagram which shows the state which carburized is started by further heating from the state shown in FIG. 転がり軸受の荷重負荷領域と浸炭深さ(浸炭層)を示す概念図である。It is a conceptual diagram which shows the load load area and carburizing depth (carburizing layer) of a rolling bearing.

以下、本発明の実施形態について詳細に説明する。
一般に、鋼材の表面から炭素を侵入させ、材料内部に拡散させる浸炭工程において、任意の深さ位置における炭素濃度の時間的変化は、Fickの第二法則を用いた(1)式で表される。(1)式によれば、浸炭工程における炭素の拡散について理論的に説明できる。
Hereinafter, embodiments of the present invention will be described in detail.
Generally, in the carburizing process in which carbon is infiltrated from the surface of a steel material and diffused into the material, the temporal change in carbon concentration at an arbitrary depth position is expressed by Eq. (1) using Fick's second law. .. According to the equation (1), the diffusion of carbon in the carburizing step can be theoretically explained.

Figure 2022000540
Figure 2022000540

C:位置xにおける炭素濃度
:表面炭素濃度
D:γ−Fe中の炭素の拡散係数
t:時間
C: Carbon concentration at position x C 0 : Surface carbon concentration D: Diffusion coefficient of carbon in γ-Fe t: Time

上記(1)式によれば、浸炭速度を向上させるには(1)表面炭素濃度C、即ち、熱処理雰囲気の炭素ポテンシャルを向上させること、又は(2)拡散係数Dが大きい高温で処理することが必要となる。 According to the above equation (1), in order to improve the carburizing rate, (1) the surface carbon concentration C 0 , that is, the carbon potential of the heat treatment atmosphere is improved, or (2) the treatment is performed at a high temperature having a large diffusion coefficient D. Is required.

実用上は、930℃〜1050℃の温度領域(肌焼き入れ鋼及び機械構造用合金鋼におけるA1点以上で共晶点以下の温度領域)での浸炭が主流であるが、更なる処理温度の高温化が可能になれば、理論的には浸炭時間は大幅に短縮できる。しかし、この技術によっても広範囲でかつ十分な浸炭深さが必要とされる部品の浸炭効率化(主に短時間での熱処理)には限界があった。 Practically, carburizing in the temperature range of 930 ° C to 1050 ° C (temperature range of A1 point or more and eutectic point or less in hardened steel and alloy steel for machine structure) is the mainstream, but further processing temperature If high temperature is possible, the carburizing time can be significantly shortened in theory. However, even with this technology, there is a limit to improving the carburizing efficiency (mainly heat treatment in a short time) of parts that require a wide range and sufficient carburizing depth.

そこで、短い浸炭時間で10mm、好ましくは15mmを超えるような浸炭深さを得るために、共晶点以上の温度域において、部品表面における浸炭反応を安定して成立させることを鋭意検討した結果、ワークを固相のオーステナイト域で加熱し、炭素源を固相及び液相からなるFe−C合金で供給する手法が適することを見出した。この手法によれば、ワーク表面の炭素濃度が、図1に示すFe−C平衡状態図のJ−E線以上に浸炭され液層が生じる課題、即ち、固溶限を超える過剰な浸炭を回避して、溶解現象のコントロールが可能となる。 Therefore, in order to obtain a carburizing depth of more than 10 mm, preferably more than 15 mm in a short carburizing time, as a result of diligent studies to stably establish a carburizing reaction on the component surface in a temperature range above the austenite. It has been found that a method of heating the work in the austenite region of the solid phase and supplying the carbon source with the Fe—C alloy consisting of the solid phase and the liquid phase is suitable. According to this method, the problem that the carbon concentration on the work surface is carburized above the JE line of the Fe-C equilibrium diagram shown in FIG. 1 to form a liquid layer, that is, excessive carburizing exceeding the solid solution limit is avoided. Then, the dissolution phenomenon can be controlled.

ワーク表面が共晶温度以上でオーステナイト固溶限以上に浸炭されると、ワーク表面に液相が発生してしまう。そこで、浸炭剤に含まれる炭素濃度と加熱温度とを制御することで、ワークとの界面の反応速度を制御する。 If the work surface is carburized above the eutectic temperature and above the austenite solid solution limit, a liquid phase will be generated on the work surface. Therefore, by controlling the carbon concentration contained in the carburizing agent and the heating temperature, the reaction rate at the interface with the work is controlled.

ここで、浸炭剤に用いるFe−C合金としては、鋳鉄粉、炭素鋼粉、工具鋼粉、鋳鉄グリッド等が使用可能である。粉(末)の形状は、粒状、針状のいずれでも良い。更に、Fe−C合金に、純鉄粉、Gr(グラファイト)粉末を混合することにより、Fe−C合金中の炭素濃度を変化させ、溶解温度をより高精度に制御することも可能である。炭素供給源となるFe−C合金粉末のC量は図1の液相出現領域(γ+L)の範囲から算出することが好ましい。 Here, as the Fe—C alloy used as the carburizing agent, cast iron powder, carbon steel powder, tool steel powder, cast iron grid and the like can be used. The shape of the powder (end) may be granular or needle-shaped. Further, by mixing pure iron powder and Gr (graphite) powder with the Fe—C alloy, it is possible to change the carbon concentration in the Fe—C alloy and control the melting temperature with higher accuracy. The amount of C in the Fe—C alloy powder as the carbon supply source is preferably calculated from the range of the liquid phase appearance region (γ + L) in FIG.

浸炭剤としてFe−C合金を主体とする粉末を用いる場合、高温まで酸化させないことが重要となる。粉末は表面積が大きく、雰囲気によっては、Fe−C合金粉末中の炭素の脱炭に伴い、溶融温度が上昇し、浸炭源を液層で供給できなくなる問題がある。このような問題に対しては、不活性ガス雰囲気中で処理することや、Fe−C合金粉末に珪酸ナトリウムや硫酸カルシウム(石膏)等の酸化防止剤を混合させることで解決できる。 When a powder mainly composed of Fe—C alloy is used as a carburizing agent, it is important not to oxidize it to a high temperature. The powder has a large surface area, and depending on the atmosphere, there is a problem that the melting temperature rises due to the decarburization of carbon in the Fe—C alloy powder, and the carburizing source cannot be supplied by the liquid layer. Such a problem can be solved by treating in an inert gas atmosphere or by mixing an antioxidant such as sodium silicate or calcium sulfate (gypsum) with the Fe—C alloy powder.

珪酸ナトリウムは、特に水溶液として供給することが好ましい。珪酸ナトリウム水溶液は、高温まで粘性のあるガラス状を呈する。Fe−C合金粉末と珪酸ナトリウム水溶液とを混練して、ワーク表面に供給することによって、Fe−C粉末自体の脱炭が抑制可能となる。 Sodium silicate is particularly preferably supplied as an aqueous solution. The sodium silicate aqueous solution exhibits a viscous glassy state up to a high temperature. By kneading the Fe—C alloy powder and the sodium silicate aqueous solution and supplying them to the work surface, decarburization of the Fe—C powder itself can be suppressed.

珪酸ナトリウムの第2の効果として、粉末状態の脱酸剤を形成できることが挙げられる。珪酸ナトリウム水溶液は、空気中のCOガスと反応して、固化する働きを持つ。したがって、Fe−C粉末同士、及びFe−C粉末とワーク表面との界面の密着性を向上させることができる。これに加え、酸素を遮断する効果も得られる。 The second effect of sodium silicate is the ability to form a powdered deoxidizer. The sodium silicate aqueous solution has a function of reacting with CO 2 gas in the air and solidifying. Therefore, it is possible to improve the adhesion between the Fe-C powders and the interface between the Fe-C powder and the work surface. In addition to this, the effect of blocking oxygen can also be obtained.

また、硫酸カルシウム(石膏)は、珪酸ナトリウムと同様に、Fe−C合金粉末同士やワーク表面との密着性を向上でき、酸素の遮断性能も得られる。 Further, calcium sulfate (gypsum), like sodium silicate, can improve the adhesion between Fe—C alloy powders and the surface of the work, and can also obtain oxygen blocking performance.

本浸炭方法は、共晶点以上の温度域において、炭素をFe−C合金として供給する方法であって、ワークの炭素濃度を固溶限濃度(図1に示すFe−C状態図のJ−E線)以下のオーステナイト域に保持することを特徴としている。また、浸炭剤に珪酸ナトリウム又は硫酸カルシウムを混合し、浸炭剤を無酸化状態にして浸炭させることを特徴としている。 This carburizing method is a method of supplying carbon as an Fe-C alloy in a temperature range above the eutectic point, and the carbon concentration of the work is set to the solid solution limit concentration (J- in the Fe-C phase diagram shown in FIG. 1). E line) It is characterized by being held in the austenite region below. Further, it is characterized in that sodium silicate or calcium sulfate is mixed with the carburizing agent to make the carburizing agent non-oxidized and carburized.

上記浸炭方法を図2,図3を用いて概念的に説明する。
図2は固相のFe−C合金粉末11と、結着剤としての珪酸ナトリウム水溶液13との混合状態の浸炭剤がワークW表面に接触した状態を示す概念図である。
ワークWは、例えば、肌焼き鋼、機械構造用合金鋼を用いた鋼製部品である。
珪酸ナトリウム水溶液13は、自身の粘着性によってFe−C合金粉末11同士を結着させるとともに、ワーク表面にFe−C合金粉末11を固着させる。このため、浸炭剤は、ワーク表面から剥がれにくくなり、ワークへの適用部位に制約を生じることがない。
The carburizing method will be conceptually described with reference to FIGS. 2 and 3.
FIG. 2 is a conceptual diagram showing a state in which a carburizing agent in a mixed state of a solid phase Fe—C alloy powder 11 and a sodium silicate aqueous solution 13 as a binder is in contact with the surface of the work W.
The work W is, for example, a steel part made of hardened steel or alloy steel for machine structure.
The sodium silicate aqueous solution 13 binds the Fe—C alloy powders 11 to each other by its own adhesiveness, and also fixes the Fe—C alloy powders 11 to the work surface. Therefore, the carburizing agent is less likely to be peeled off from the surface of the work, and there is no restriction on the application site to the work.

図2の状態から加熱すると、図3に示すように、浸炭剤は、Fe−C合金粉末11の一部が溶融して、固相のFe−C合金粉末11及び液相のFe−C合金15と、結着剤としての珪酸ナトリウム水溶液13が混合状態となってワークW表面に接触する。この場合、液相となったFe−C合金15が、ワーク表面に広がって接触することで、浸炭剤とワークWとの接触面積が増加し、ワークWへの炭素供給速度が大幅に向上する。しかも、共晶点以上に加熱した場合に、珪酸ナトリウム水溶液13の作用によって、Fe−C合金の脱炭が抑制できるため、ワーク表面は浸炭が促進する。その結果、Fe−C合金の溶融温度の上昇を防止し、浸炭源を液相で供給しやすくなる。 When heated from the state of FIG. 2, as shown in FIG. 3, the carburizing agent melts a part of the Fe—C alloy powder 11 to form a solid phase Fe—C alloy powder 11 and a liquid phase Fe—C alloy. 15 and the aqueous sodium silicate solution 13 as a binder are in a mixed state and come into contact with the surface of the work W. In this case, the Fe-C alloy 15 that has become a liquid phase spreads and contacts the surface of the work, so that the contact area between the carburizing agent and the work W increases, and the carbon supply rate to the work W is significantly improved. .. Moreover, when heated above the eutectic point, decarburization of the Fe—C alloy can be suppressed by the action of the sodium silicate aqueous solution 13, so that carburization of the work surface is promoted. As a result, the increase in the melting temperature of the Fe—C alloy is prevented, and the carburizing source can be easily supplied in the liquid phase.

なお、図3の状態から更に固相のFe−C合金粉末11が液相化して、浸炭剤が液相のFe−C合金15と結着剤との混合状態になることも考えられる。その場合でも、結着剤である珪酸ナトリウム水溶液13は、Fe−C合金の酸化防止剤として機能して、Fe−C合金の溶融温度の上昇を防止できる。 It is also conceivable that the solid phase Fe—C alloy powder 11 is further liquid-phased from the state of FIG. 3, and the carburizing agent is in a mixed state of the liquid-phase Fe—C alloy 15 and the binder. Even in that case, the sodium silicate aqueous solution 13 as a binder functions as an antioxidant of the Fe—C alloy and can prevent the melting temperature of the Fe—C alloy from rising.

上記浸炭方法の効果を確認するため、転がり軸受の表層部を模擬した試験片を用い、以下の実験を行った。実施例としては、JIS G 4053(機械構造用合金鋼鋼材)のSCr420鋼材(炭素0.18〜0.23%、中央値0.205%、オーステナイト域880〜1470℃)を選定し、外径φ20mm、内径φ15mmの止まり穴を有する試験片を作製した。 In order to confirm the effect of the above carburizing method, the following experiment was conducted using a test piece simulating the surface layer of the rolling bearing. As an example, SCr420 steel material (carbon 0.18 to 0.23%, median 0.205%, austenite region 880 to 1470 ° C.) of JIS G 4053 (alloy steel material for machine structure) was selected, and the outer diameter was selected. A test piece having a blind hole having a diameter of 20 mm and an inner diameter of φ15 mm was produced.

浸炭剤は、炭素材をFe−3.1%Cの粉末とし、10重量%の珪酸ナトリウム水溶液と混練した。Fe−3.1%Cの粉末を9g含むこの浸炭剤10gを上記試験片の被浸炭面に密着させた。その後、窒素ガス雰囲気中で1200℃(Fe−C平衡状態図よりSCr420鋼材の共晶点1147℃、包晶点1494℃の中間温度)で30分加熱保持して浸炭処理を実施し、炉内で冷却した。 As the carburizing agent, the carbon material was made into a powder of Fe-3.1% C and kneaded with a 10% by weight aqueous sodium silicate solution. 10 g of this carburizing agent containing 9 g of Fe-3.1% C powder was brought into close contact with the carburized surface of the test piece. After that, carburizing was carried out by heating and holding at 1200 ° C. (intermediate temperature of eutectic point 1147 ° C. and peritectic point 1494 ° C. of SCr420 steel material from the Fe-C equilibrium phase diagram) for 30 minutes in a nitrogen gas atmosphere. Cooled with.

比較例としては、実施例と同様にSCr420鋼材からなる転がり軸受の表層部を模擬した試験片を作製し、Rxガス(吸熱型変成ガス)+エンリッチガス雰囲気中でカーボンポテンシャルを1.05として、950℃(Fe−C平衡状態図よりSCr429鋼材の共晶点1147℃未満の温度)で実施例の10倍に相当する5時間のガス浸炭を実施した後、油冷して、一般的な大型軸受の浸炭処理であるガス浸炭を模擬した。 As a comparative example, a test piece simulating the surface layer of a rolling bearing made of SCr420 steel was prepared in the same manner as in the example, and the carbon potential was set to 1.05 in an atmosphere of Rx gas (heat absorbing type modified gas) + enriched gas. After performing gas carburizing for 5 hours at 950 ° C (the temperature of the eutectic point of SCr429 steel material less than 1147 ° C from the Fe-C phase diagram), which is 10 times that of the example, it is oil-cooled and is generally large. Gas carburizing, which is a carburizing process for bearings, was simulated.

実験による浸炭効果は、それぞれの試験片の断面をEPMA分析し、C%プロファイルから全浸炭深さを求め、F.E.Harrisの実験式(x=K√t)における浸炭速度定数Kを求めた。 For the carburizing effect by the experiment, EPMA analysis was performed on the cross section of each test piece, and the total carburizing depth was obtained from the C% profile. E. The carburizing rate constant K in Harris's empirical formula (x = K√t) was determined.

以上の比較実験の結果を表1に纏めて示す。 The results of the above comparative experiments are summarized in Table 1.

Figure 2022000540
Figure 2022000540

実施例では、浸炭速度定数K=2.69となり、比較例(従来法)のガス浸炭における浸炭速度定数K=0.76に対して迅速な浸炭となることが確認できた。即ち、従前では1.7mmの浸炭深さを得るのに5時間を要していたところ、本浸炭方法によれば、僅か0.5時間で比較例の浸炭深さを超える1.9mmの浸炭深さが得られることになる。 In the example, the carburizing rate constant K = 2.69, and it was confirmed that the carburizing was rapid with respect to the carburizing rate constant K = 0.76 in the gas carburizing of the comparative example (conventional method). That is, in the past, it took 5 hours to obtain a carburizing depth of 1.7 mm, but according to this carburizing method, a carburizing depth of 1.9 mm, which exceeds the carburizing depth of the comparative example, is only 0.5 hours. Depth will be obtained.

従前、高温ではオーステナイトに固溶する炭素量が多いため、固体浸炭では過剰浸炭になりやすい。そのため、高温浸炭の場合は、カーボンポテンシャルを制御しやすいガス浸炭に限られていた。一方、本浸炭方法では、珪酸ナトリウムを用いることで、オーステナイト域における高温浸炭時のカーボンポテンシャルを高精度に制御可能にしている。珪酸ナトリウムは、従前より浸炭防止剤として用いられるが、このような浸炭防止剤を用いてカーボンポテンシャルを制御する技術は、他に見当たらない。本浸炭方法は、浸炭防止剤の高温粘性が高い性質を利用して、高温浸炭時に浸炭剤がワーク表面に密着し続けて深い浸炭層を形成するという、低コストで画期的な浸炭方法である。 In the past, at high temperatures, the amount of carbon that dissolves in austenite is large, so solid carburizing tends to result in excessive carburizing. Therefore, in the case of high temperature carburizing, it was limited to gas carburizing in which the carbon potential can be easily controlled. On the other hand, in this carburizing method, by using sodium silicate, it is possible to control the carbon potential at the time of high temperature carburizing in the austenite region with high accuracy. Sodium silicate has been used as a carburizing inhibitor for some time, but there is no other technique for controlling carbon potential using such an anticarburizing agent. This carburizing method is a low-cost and epoch-making carburizing method that utilizes the high high-temperature viscosity of the carburizing inhibitor to keep the carburizing agent in close contact with the work surface during high-temperature carburizing to form a deep carburized layer. be.

また、浸炭剤が固相及び液相の混合状態であることで、ワーク表面と浸炭剤が広範囲に接触する状態となり、全てが固相の場合と比較して、均一に浸炭が可能となる。よって、高品位な浸炭処理を短時間で実現できる。 Further, when the carburizing agent is in a mixed state of the solid phase and the liquid phase, the work surface and the carburizing agent come into contact with each other in a wide range, and the carburizing can be performed uniformly as compared with the case where all of them are in the solid phase. Therefore, high-quality carburizing can be realized in a short time.

このように、本浸炭方法によれば、高温浸炭時におけるガス浸炭の炭素ポテンシャルと比較して高い炭素ポテンシャル状態を維持でき、例えば大型の広範囲でかつ十分な浸炭深さが必要な転がり軸受において、従前よりも大幅に時間短縮した浸炭が可能となる。 As described above, according to this carburizing method, a high carbon potential state can be maintained as compared with the carbon potential of gas carburizing at the time of high temperature carburizing, for example, in a large rolling bearing that requires a wide range and sufficient carburizing depth. Carburizing is possible in a significantly shorter time than before.

また、酸化防止剤として用いる珪酸ナトリウム、及び珪酸ナトリウム水溶液としては、JIS K 1408に記載のように、1〜3号の水ガラス(珪酸ナトリウム水溶液)、メタ珪酸ナトリウム1、2号(結晶)を用いることができる。
硫酸カルシウムとしては、JIS R 9111に記載のように、特級〜B級の陶磁器型材用せっこうを用いることができる。
As the sodium silicate used as an antioxidant and the sodium silicate aqueous solution, as described in JIS K 1408, water glass Nos. 1 to 3 (sodium silicate aqueous solution) and sodium metasilicates Nos. 1 and 2 (crystals) are used. Can be used.
As the calcium sulfate, as described in JIS R 9111, gypsum for special grade to B grade ceramic mold materials can be used.

炭素材であるFe−C合金には、その他の元素を含んでも構わない。本構成では、炉加熱による加熱方式としているが、高周波加熱も使用可能である。不活性ガスとしては、工業的にはNガスやCOガスを主体とする還元性の変成ガスを用いることができる。 The Fe—C alloy, which is a carbon material, may contain other elements. In this configuration, the heating method is based on furnace heating, but high-frequency heating can also be used. The inert gas, in industry can be used reducing reformed gas mainly composed of N 2 gas and CO gas.

このように、本発明は上記の実施形態に限定されるものではなく、実施形態の各構成を相互に組み合わせることや、明細書の記載、並びに周知の技術に基づいて、当業者が変更、応用することも本発明の予定するところであり、保護を求める範囲に含まれる。 As described above, the present invention is not limited to the above-described embodiment, and can be modified or applied by those skilled in the art based on the mutual combination of the configurations of the embodiments, the description of the specification, and the well-known technique. It is also a matter of the present invention to do so, and it is included in the scope of seeking protection.

以上の通り、本明細書には次の事項が開示されている。
(1) 粉末状のFe−C合金と、前記粉末状のFe−C合金の粉末同士を結着させる結着剤とを含む浸炭剤を、少なくとも一部の表面に接触させた鋼製部品を、
前記鋼製部品の共晶点以上、包晶点未満のオーステナイト域の温度範囲に一定時間保持する、鋼製部品の浸炭方法。
この鋼製部品の浸炭方法によれば、過剰浸炭を回避しつつ、深い浸炭深さが短時間で形成できる。また、浸炭時にFe−C合金の粉末同士を結着させ、鋼製部品の表面に浸炭剤を密着させた状態にできる。そのため、重力や加熱等の要因によって鋼製部品から浸炭剤が剥がれることがなく、鋼製部品の確実な浸炭処理が行える。
As described above, the following matters are disclosed in this specification.
(1) A steel part in which a carburizing agent containing a powdery Fe-C alloy and a binder for binding the powdered Fe-C alloy powder to each other is brought into contact with at least a part of the surface. ,
A method for carburizing a steel part, which maintains the temperature in the austenite region above the eutectic point and below the peritectic point for a certain period of time.
According to this carburizing method for steel parts, a deep carburizing depth can be formed in a short time while avoiding excessive carburizing. Further, at the time of carburizing, the powders of Fe—C alloy can be bonded to each other so that the carburizing agent is in close contact with the surface of the steel part. Therefore, the carburizing agent does not peel off from the steel parts due to factors such as gravity and heating, and the steel parts can be reliably carburized.

(2) 前記浸炭剤は、前記共晶点以上で、前記Fe−C合金が固相と液相との混合状態で含まれる(1)に記載の鋼製部品の浸炭方法。
この鋼製部品の浸炭方法によれば、高品位な浸炭処理を短時間で実現できる。
(2) The method for carburizing steel parts according to (1), wherein the carburizing agent has a eutectic point or higher and contains the Fe—C alloy in a mixed state of a solid phase and a liquid phase.
According to this carburizing method for steel parts, high-quality carburizing can be realized in a short time.

(3) 前記結着剤は、前記共晶点以上で、前記Fe−C合金の酸化防止機能を有する(2)に記載の鋼製部品の浸炭方法。
この鋼製部品の浸炭方法によれば、酸化防止機能を有することで、Fe−C合金の融点上昇が抑制され、Fe−C合金の液相化に影響を及ぼすことがない。
(3) The method for carburizing steel parts according to (2), wherein the binder has a eutectic point or higher and has an antioxidant function of the Fe—C alloy.
According to this method of carburizing steel parts, having an antioxidant function suppresses an increase in the melting point of the Fe—C alloy and does not affect the liquid phase formation of the Fe—C alloy.

(4) 前記結着剤は、珪酸ナトリウム、硫酸カルシウムのいずれかを含む(3)に記載の鋼製部品の浸炭方法。
この鋼製部品の浸炭方法によれば、低コストで確実な浸炭処理が行える。
(4) The method for carburizing steel parts according to (3), wherein the binder contains either sodium silicate or calcium sulfate.
According to this carburizing method for steel parts, reliable carburizing can be performed at low cost.

(5) 前記結着剤は、珪酸ナトリウム水溶液である(3)に記載の鋼製部品の浸炭方法。
この鋼製部品の浸炭方法によれば、Fe−C粉末同士を、粘性を伴って確実に結着させることができる。
(5) The method for carburizing steel parts according to (3), wherein the binder is an aqueous solution of sodium silicate.
According to this method of carburizing steel parts, Fe-C powders can be reliably bonded to each other with viscosity.

(6) 前記鋼製部品を不活性ガス雰囲気中で加熱する(1)〜(5)のいずれか一つに記載の鋼製部品の浸炭方法。
この鋼製部品の浸炭方法によれば、Fe−C合金の脱炭が抑制され、溶融温度の上昇を防止できるため、浸炭源を液相で供給しやすくなる。
(6) The method for carburizing a steel part according to any one of (1) to (5), wherein the steel part is heated in an atmosphere of an inert gas.
According to this carburizing method for steel parts, decarburization of the Fe—C alloy can be suppressed and an increase in the melting temperature can be prevented, so that the carburizing source can be easily supplied in the liquid phase.

(7) 粉末状のFe−C合金と、前記粉末状のFe−C合金の粉末同士を結着させる結着剤とを含む浸炭剤を、少なくとも一部の表面に接触させた鋼製部品を、
前記鋼製部品の共晶点以上、包晶点未満のオーステナイト域の温度範囲に一定時間保持させて得た、鋼製部品。
この鋼製部品によれば、耐摩耗性、摺動性、疲労強度に優れた浸炭層が短時間で深い領域まで形成される。
(7) A steel part in which a carburizing agent containing a powdery Fe-C alloy and a binder for binding the powdered Fe-C alloy powder to each other is brought into contact with at least a part of the surface thereof. ,
A steel part obtained by holding the steel part in the temperature range of the austenite region having the eutectic point or more and less than the peritectic point for a certain period of time.
According to this steel part, a carburized layer having excellent wear resistance, slidability, and fatigue strength is formed in a deep region in a short time.

(8) 粉末状のFe−C合金と、前記粉末粒子同士を鋼材の共晶点以上で結着させる結着剤と、を含む浸炭剤。
この浸炭剤によれば、鋼材の過剰浸炭を回避しつつ、深い浸炭深さが短時間で形成できる。
(8) A carburizing agent containing a powdery Fe-C alloy and a binder for binding the powder particles to each other at a eutectic point or higher of a steel material.
According to this carburizing agent, a deep carburizing depth can be formed in a short time while avoiding excessive carburizing of the steel material.

11 Fe−C合金粉末(固相)
13 珪酸ナトリウム水溶液
15 Fe−C合金(液相)
W ワーク
11 Fe-C alloy powder (solid phase)
13 Sodium silicate aqueous solution 15 Fe-C alloy (liquid phase)
W work

Claims (5)

粉末状のFe−C合金と、前記粉末状のFe−C合金の粉末同士を結着させる珪酸ナトリウム水溶液から成る結着剤とを混練した浸炭剤を、鋼製部品の少なくとも一部の表面に接触させ、前記鋼製部品を素材の共晶点以上、包晶点未満のオーステナイト域の温度範囲に一定時間保持し、少なくとも1.9mm以上の浸炭深さの浸炭層を形成する、鋼製部品の浸炭方法。 A carburizing agent obtained by kneading a powdered Fe-C alloy and a binder composed of an aqueous sodium silicate that binds the powders of the powdered Fe-C alloy to each other is applied to the surface of at least a part of the steel part. Steel parts that are brought into contact with each other to hold the steel parts in the temperature range of the austenite region above the eutectic point and below the peritectic point for a certain period of time to form a carburized layer with a carburizing depth of at least 1.9 mm. Carburizing method. 前記浸炭剤は、前記共晶点以上で、前記Fe−C合金が固相と液相との混合状態で含まれる請求項1に記載の鋼製部品の浸炭方法。 The method for carburizing a steel part according to claim 1, wherein the carburizing agent has a eutectic point or higher and the Fe—C alloy is contained in a mixed state of a solid phase and a liquid phase. 前記結着剤は、前記共晶点以上で、前記Fe−C合金の酸化防止機能を有する請求項1に記載の鋼製部品の浸炭方法。 The method for carburizing a steel part according to claim 1, wherein the binder has a eutectic point or higher and has an antioxidant function of the Fe—C alloy. 前記鋼製部品を不活性ガス雰囲気中で加熱する請求項1〜請求項3のいずれか一項に記載の鋼製部品の浸炭方法。 The method for carburizing a steel part according to any one of claims 1 to 3, wherein the steel part is heated in an atmosphere of an inert gas. 浸炭層を備える鋼製部品の製造方法であって、
粉末状のFe−C合金と、珪酸ナトリウム水溶液から成る結着剤とを混練した浸炭剤を鋼製部品の少なくとも一部の表面に接触させ、前記鋼製部品を素材の共晶点以上、包晶点未満のオーステナイト域の温度範囲に一定時間保持し、少なくとも1.9mm以上の浸炭深さの前記浸炭層を形成する、鋼製部品の製造方法。
A method for manufacturing steel parts with a carburized layer.
A carburizing agent obtained by kneading a powdery Fe-C alloy and a binder composed of an aqueous solution of sodium silicate is brought into contact with the surface of at least a part of the steel parts, and the steel parts are packaged at or above the eutectic point of the material. A method for manufacturing a steel part, which is maintained in a temperature range in the austenite region below the crystal point for a certain period of time to form the carburized layer having a carburized depth of at least 1.9 mm or more.
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