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JPH0454736B2 - - Google Patents
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JPH0454736B2 - - Google Patents

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Publication number
JPH0454736B2
JPH0454736B2 JP58104277A JP10427783A JPH0454736B2 JP H0454736 B2 JPH0454736 B2 JP H0454736B2 JP 58104277 A JP58104277 A JP 58104277A JP 10427783 A JP10427783 A JP 10427783A JP H0454736 B2 JPH0454736 B2 JP H0454736B2
Authority
JP
Japan
Prior art keywords
carburizing
steel
parts
carbon potential
hardness
Prior art date
Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
Expired - Lifetime
Application number
JP58104277A
Other languages
Japanese (ja)
Other versions
JPS59232252A (en
Inventor
Katsunori Takada
Kenji Isogawa
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
Daido Steel Co Ltd
Original Assignee
Daido Steel Co Ltd
Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)
Filing date
Publication date
Application filed by Daido Steel Co Ltd filed Critical Daido Steel Co Ltd
Priority to JP10427783A priority Critical patent/JPS59232252A/en
Publication of JPS59232252A publication Critical patent/JPS59232252A/en
Publication of JPH0454736B2 publication Critical patent/JPH0454736B2/ja
Granted legal-status Critical Current

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Description

【発明の詳細な説明】[Detailed description of the invention]

この発明は浸炭用鋼に関し、とくに浸炭処理後
の表面の浸炭層硬さが大であり、耐ピツチング性
および疲労強度に優れた浸炭部品の素材に適する
浸炭用鋼に関するものである。 従来、機械構造用部品、例えばギヤ、コンロツ
ド、ピニオン、ラツク、ベアリング、ベアリング
レース、ステアリング部品等の構造部品は、表面
の耐摩耗性および疲労強度を高めるために、浸炭
処理を施すことが多い。このような浸炭処理が施
される部品の素材としては、従来、JISに規定す
るSC材、SCr材、SCM材、SMn材、SNC材、
SNCM材等の構造用鋼が使用されるのが普通で
ある。 一方、近年とくに自動車の走行性能および燃料
経済性の向上をはかるために、自動車部品の軽量
化が指向されるようになつてきており、特に浸炭
処理して使用される上記ギヤ、コンロツド等のパ
ワートレーン系部品においてもそれらの小型化が
求められるようになつてきている。しかしなが
ら、前記した従来の構造用鋼に対して通常の浸炭
処理を施したときには、特に部品が小型化されて
いる場合に十分な強度が得られないという問題が
あつた。 そのため、小型化した部品の強度とくに耐ピツ
チング性や疲れ強さを高めることが望まれてお
り、なかでも耐ピツチング性を向上させるために
表面硬度を高める過剰浸炭を施すことも考えられ
た。しかしながら、上述した従来の構造用鋼に対
して過剰浸炭を施そうとする場合には、雰囲気の
カーボンポテンシヤルがおよそ3%以上となるよ
うにする必要があるため、通常の浸炭処理の範疇
から外れることとなり、浸炭処理作業性が著しく
低下するという問題があつた。 このような高いカーボンポテンシヤルで過剰浸
炭を行うことを特徴とした特殊用途鋼の開発もあ
るが、これは圧延ロール等の大型部品を対象とし
たものであつて、Cr、Moを多量に含有するもの
であり、価格が高いという欠点を有しているほ
か、特に自動車部品等の小型部品にこの特殊用途
鋼を適用した場合には、上述したようにCr、Mo
の含有量が多いために焼入性が良すぎるので、浸
炭処理時に部品の中心部まで焼入れされることと
なり、例えばギヤに適用したときには歯元の残留
応力が少なくなるためその強度が低下するという
問題があつた。 この発明は上記したような従来の問題点に着目
してなされたもので、浸炭雰囲気のカーボンポテ
ンシヤルが2.5%以下程度の通常の浸炭処理を施
したときでも過剰浸炭が可能であり、表面の硬度
を著しく高めることが可能であつて、耐ピツチン
グ性や疲労強度に優れた浸炭部品を得ることが可
能である浸炭用鋼を提供することを目的としてい
る。 この発明による浸炭用鋼は、重量%で、C:
0.1〜0.3%、Mn:0.2〜1.5%、Cr:1〜3%で且
つMn+Cr≦3%を含み、さらに、Si:0.5〜1.5
%、Al:0.2〜1.5%を含有し、必要に応じて、
Mo:0.1〜0.5%、V:0.1〜0.5%、Ti:0.1〜0.5
%、Zr:0.1〜0.5%、Nb+Ta(いずれか一方が0
の場合を含む):0.1〜0.5%のうちの1種または
2種以上を含有し、残部Feおよび不純物からな
り、より望ましくはカーボンポテンシヤルが1.0
〜2.5%の浸炭雰囲気中での浸炭処理後の浸炭層
に微細な球状炭化物が析出することを特徴として
いる。 次に、この発明による浸炭用鋼の成分範囲(重
量%)の限度理由について説明する。 C:0.1〜0.3% Cは構造部品として必要な強度ならびに浸炭処
理後の表面硬さを得るために含有させる元素であ
るが、含有量が0.1%よりも少ないと上記した必
要な強度ならびに表面硬さを得ることができず、
0.3%を超えると靭性ならびに冷鍛性が低下する
ので、0.1〜0.3%の範囲とした。 Mn:0.2〜1.5% Mnは鋼溶製時の脱酸および脱硫元素として有
効であるが、0.2%よりも少ないと上記の脱酸お
よび脱硫効果が小さく、また浸炭処理後の表面硬
さも十分なものが得られない。一方、1.5%を超
えると焼入性の制御が困難になるとともに加工性
ならびに被削性が劣化する。したがつて、Mn含
有量は0.2〜1.5%の範囲とした。 Cr:1〜3% Crは炭化物を析出して浸炭処理後の浸炭層の
硬度を高めるために有効な元素であり、このよう
な効果を得るために1%以上含有させる。しか
し、Cr含有量が多くなりすぎると焼入性の制御
が困難になるので、1〜3%の範囲とした。 Mn+Cr≦3% MnおよびCr含有量が多すぎると、上記したよ
うに鋼の焼入制の制御が困難となり、例えばギヤ
等に適用する場合に焼入性が過大であるため歯元
の残留応力が小さくなつて強度が低下するので、
MnおよびCrの合計量についても上限を設定する
必要があり、Mn+Crの合計を3%以下とした。 Si:0.5〜1.5% Al:0.2〜1.5% SiおよびAlはいずれもCr炭化物の析出を促進
して浸炭層硬さを十分に確保するのに必要であつ
て、このためには、Siについては0.5%以上、Al
については0.2%以上含有させる必要がある。し
かし、含有量が多すぎると靭性を劣化するので、
Siについては1.5%以下、Alについても1.5%以下
とする必要がある。 Mo:0.1〜0.5%、V:0.1〜0.5%、Ti:0.1〜
0.5%、Zr:0.1〜0.5%、Nb+Ta:0.1〜0.5%の
うちの1種または2種以上 Mo、V、Ti、Nb、Taはいずれも高温での浸
炭処理時にオーステナイト結晶粒の粗大化を防止
するのに有効な元素であるので、必要に応じて
各々0.1%以上含有させることが好ましい。しか
し、含有量が各々0.5%を超えると結晶粒粗大化
の防止効果がかえつて低下するため、それぞれ
0.1〜0.5%(Nb、Taはいずれか一方が0である
場合を含む。)の範囲とする。 このように成分調整した鋼を素材とし、ギヤ、
ボールジヨイント、ドライブシヤフト、カムシヤ
フト、ステアリング部品、ベアリング、ベアリン
グレース等の構造部品を成形加工し、その後より
望ましくは浸炭雰囲気のカーボンポテンシヤルが
1.0〜2.5%である雰囲気中で浸炭処理を施すこと
によつて、表面の浸炭層に微細な球状炭化物が析
出しており、表面硬度が大であつて耐ピツチング
性や疲労強度等に優れ、寸法精度の良好な構造部
品を得る。ここで、浸炭雰囲気のカーボンポテン
シヤルが1.0〜2.5%であることがより望ましいの
は、カーボンポテンシヤルが低すぎると過剰浸炭
が困難となり、浸炭によつて表面の硬度を高める
ことができなくなるためであり、他方、カーボン
ポテンシヤルが高すぎると通常の簡便な浸炭処理
ができなくなり、処理コストが著しく高くなるた
めである。 以下、この発明の実施例を比較例とともに説明
する。 第1表に示す化学成分の鋼を溶製したのち造塊
し、次いで分塊圧延、製品圧延して直径25mm、長
さ75mmの試験片を作製した。次に、各試験片を第
2表に示すカーボンポテンシヤルの浸炭雰囲気中
で925℃×5時間加熱→830℃油冷(油温70℃)→
170℃×1時間加熱→空冷の条件で浸炭焼入れ。
焼もどし処理を行い、各試験片の浸炭層を組織観
察すると共に、表層より深さ0.1mmにおける浸炭
層硬さを測定した。この結果を第2表に示す。
The present invention relates to a carburizing steel, and particularly to a carburizing steel that has a high hardness of the carburized layer on the surface after carburizing treatment and is suitable as a material for carburized parts having excellent pitting resistance and fatigue strength. Conventionally, mechanical structural parts such as gears, connecting rods, pinions, racks, bearings, bearing races, and steering parts are often carburized to increase their surface wear resistance and fatigue strength. Conventionally, the materials for parts that are subjected to carburizing treatment include SC material, SCr material, SCM material, SMn material, SNC material, specified by JIS.
Structural steel such as SNCM material is usually used. On the other hand, in recent years, in order to improve the driving performance and fuel economy of automobiles, there has been an increasing trend towards reducing the weight of automobile parts. There is also a growing demand for miniaturization of train-related parts. However, when the above-mentioned conventional structural steel is subjected to normal carburizing treatment, there is a problem that sufficient strength cannot be obtained, especially when the parts are downsized. Therefore, it is desired to increase the strength of miniaturized parts, especially pitting resistance and fatigue strength, and in order to improve pitting resistance, excessive carburizing to increase surface hardness has been considered. However, when attempting to excessively carburize the conventional structural steel mentioned above, it is necessary to ensure that the carbon potential of the atmosphere is approximately 3% or more, which is outside the scope of normal carburizing treatment. As a result, there was a problem in that the workability of carburizing treatment was significantly reduced. Special-purpose steels have been developed that are characterized by excessive carburization with such high carbon potential, but these are intended for large parts such as rolling rolls, and they contain large amounts of Cr and Mo. In addition to the disadvantage of high price, especially when this special purpose steel is applied to small parts such as automobile parts, it is difficult to use Cr, Mo, etc. as mentioned above.
Because of its high content, it has very good hardenability, so during the carburizing process, the center of the part is hardened, and when applied to gears, for example, the residual stress at the root of the tooth decreases, reducing its strength. There was a problem. This invention was made by focusing on the above-mentioned conventional problems, and it is possible to carry out excessive carburization even when performing normal carburizing treatment in which the carbon potential of the carburizing atmosphere is about 2.5% or less, and the surface hardness can be reduced. It is an object of the present invention to provide a carburizing steel that can significantly increase the carburizing properties and yield carburized parts with excellent pitting resistance and fatigue strength. The carburizing steel according to the invention has C:
0.1 to 0.3%, Mn: 0.2 to 1.5%, Cr: 1 to 3%, and contains Mn + Cr≦3%, and furthermore, Si: 0.5 to 1.5
%, Al: Contains 0.2-1.5%, if necessary,
Mo: 0.1-0.5%, V: 0.1-0.5%, Ti: 0.1-0.5
%, Zr: 0.1~0.5%, Nb+Ta (one of them is 0)
): Contains one or more of 0.1 to 0.5%, with the remainder consisting of Fe and impurities, and more preferably has a carbon potential of 1.0.
It is characterized by the precipitation of fine spherical carbides in the carburized layer after carburizing in a ~2.5% carburizing atmosphere. Next, the reason for the limit on the composition range (wt%) of the steel for carburizing according to the present invention will be explained. C: 0.1-0.3% C is an element to be included to obtain the strength required for structural parts and surface hardness after carburizing treatment, but if the content is less than 0.1%, the above-mentioned required strength and surface hardness will be reduced. I can't get the feeling,
If it exceeds 0.3%, toughness and cold forgeability will deteriorate, so it is set in the range of 0.1 to 0.3%. Mn: 0.2-1.5% Mn is effective as a deoxidizing and desulfurizing element during steel making, but if it is less than 0.2%, the above deoxidizing and desulfurizing effects will be small, and the surface hardness after carburizing will not be sufficient. I can't get anything. On the other hand, if it exceeds 1.5%, it becomes difficult to control hardenability and workability and machinability deteriorate. Therefore, the Mn content was set in the range of 0.2 to 1.5%. Cr: 1 to 3% Cr is an effective element for precipitating carbides and increasing the hardness of the carburized layer after carburizing treatment, and is contained in an amount of 1% or more to obtain this effect. However, if the Cr content becomes too large, it becomes difficult to control the hardenability, so it is set in the range of 1 to 3%. Mn+Cr≦3% If the Mn and Cr contents are too high, it becomes difficult to control the hardening of the steel as described above, and when applied to gears, for example, the hardenability is excessive, resulting in residual stress at the root of the tooth. becomes smaller and the strength decreases, so
It is also necessary to set an upper limit for the total amount of Mn and Cr, and the total of Mn+Cr is set to 3% or less. Si: 0.5-1.5% Al: 0.2-1.5% Both Si and Al are necessary to promote the precipitation of Cr carbides and ensure sufficient hardness of the carburized layer. 0.5% or more, Al
It is necessary to contain 0.2% or more. However, if the content is too high, the toughness will deteriorate, so
The content of Si must be 1.5% or less, and the content of Al must also be 1.5% or less. Mo: 0.1~0.5%, V: 0.1~0.5%, Ti: 0.1~
One or more of the following: 0.5%, Zr: 0.1~0.5%, Nb+Ta: 0.1~0.5% Mo, V, Ti, Nb, and Ta all cause coarsening of austenite crystal grains during carburizing treatment at high temperatures. Since these elements are effective in preventing the above, it is preferable to contain each of them in an amount of 0.1% or more, if necessary. However, if the content exceeds 0.5% of each, the effect of preventing crystal grain coarsening will decrease, so each
The range is 0.1 to 0.5% (including cases where either Nb or Ta is 0). Gears,
Structural parts such as ball joints, drive shafts, camshafts, steering parts, bearings, and bearing races are molded and then, more preferably, carbon potential in a carburizing atmosphere is formed.
By performing carburizing treatment in an atmosphere with a concentration of 1.0 to 2.5%, fine spherical carbides are precipitated in the carburized layer on the surface, resulting in high surface hardness and excellent pitting resistance and fatigue strength. Obtain structural parts with good dimensional accuracy. Here, it is more desirable that the carbon potential of the carburizing atmosphere is 1.0 to 2.5% because if the carbon potential is too low, excessive carburization becomes difficult and it becomes impossible to increase the surface hardness by carburizing. On the other hand, if the carbon potential is too high, ordinary and simple carburizing treatment cannot be carried out, and the treatment cost becomes extremely high. Examples of the present invention will be described below along with comparative examples. Steel having the chemical composition shown in Table 1 was melted and then formed into ingots, followed by blooming and rolling to produce test pieces with a diameter of 25 mm and a length of 75 mm. Next, each test piece was heated at 925°C for 5 hours in a carburizing atmosphere with the carbon potential shown in Table 2 → oil-cooled at 830°C (oil temperature 70°C) →
Carburizing and quenching under the conditions of heating at 170℃ for 1 hour and cooling in the air.
After tempering, the structure of the carburized layer of each specimen was observed, and the hardness of the carburized layer at a depth of 0.1 mm from the surface layer was measured. The results are shown in Table 2.

【表】【table】

【表】 第1表および第2表から明らかなように、この
発明による浸炭溶鋼(No.2〜13)では、カーボン
ポテンシヤルが1.25%の浸炭雰囲気中で浸炭した
場合に、浸炭層に微細な球状炭化物が析出してお
り、浸炭層の硬さも著しく大きなものとなつてお
り、ギヤ等に適用した場合に耐ピツチング性や疲
労強度をかなり高めることができるという結果が
得られた。一方、浸炭雰囲気中のカーボンポテン
シヤルが低すぎる場合には過剰浸炭による表面硬
さの増大が得られないこともわかつた。さらに、
この発明の成分範囲を満足しない鋼(No.1)では
浸炭雰囲気中のカーボンポテンシヤルを1.25%と
しても過剰浸炭層が形成されず、十分な表面硬さ
を得ることができなかつた。 次に、一般のガス浸炭においてカーボンポテン
シヤルを高めたときにはスーテイングが発生しや
すいが、真空浸炭ではこのようなスーテイングの
発生はないので、カーボンポテンシヤルを比較的
容易に高めることが可能である。したがつて、こ
のような観点からは過剰浸炭させる場合に真空浸
炭を施すことがより望ましく、以下に真空浸炭し
た場合の実施例を比較例と共に説明する。 まず、第1表に示すNo.1、2、5、6、8、10
の鋼から前記実施例および比較例と同様にして作
製した直径25mm、長さ75mmの各試験片をカーボン
ポテンシヤルが1.7%の浸炭雰囲気中で真空浸炭
処理を行つた。この真空浸炭処理では、上記雰囲
気中で、1040℃×1.5時間加熱→830℃油冷の焼入
れ→170℃×1時間の焼もどしの条件で行つた。
その後、各試験片の浸炭層を組織観察すると共
に、表層より深さ0.1mmにおける浸炭層硬さを測
定した。この結果を第3表に示す。
[Table] As is clear from Tables 1 and 2, when carburized molten steel (Nos. 2 to 13) according to the present invention is carburized in a carburizing atmosphere with a carbon potential of 1.25%, fine particles are formed in the carburized layer. Spheroidal carbides were precipitated, and the hardness of the carburized layer was significantly increased, and the results showed that pitting resistance and fatigue strength could be significantly improved when applied to gears, etc. On the other hand, it was also found that if the carbon potential in the carburizing atmosphere was too low, an increase in surface hardness due to excessive carburization could not be obtained. moreover,
In steel (No. 1) that did not satisfy the composition range of this invention, an excessive carburized layer was not formed even when the carbon potential in the carburizing atmosphere was 1.25%, and sufficient surface hardness could not be obtained. Next, sooting tends to occur when the carbon potential is increased in general gas carburizing, but such sooting does not occur in vacuum carburizing, so it is possible to increase the carbon potential relatively easily. Therefore, from this point of view, it is more desirable to perform vacuum carburization when excessive carburization is performed, and examples in which vacuum carburization is performed will be described below together with comparative examples. First, No. 1, 2, 5, 6, 8, 10 shown in Table 1
Each test piece with a diameter of 25 mm and a length of 75 mm was prepared from steel in the same manner as in the above Examples and Comparative Examples and was subjected to vacuum carburizing treatment in a carburizing atmosphere with a carbon potential of 1.7%. This vacuum carburizing treatment was carried out in the above atmosphere under the following conditions: heating at 1040°C for 1.5 hours, quenching at 830°C with oil cooling, and tempering at 170°C for 1 hour.
Thereafter, the structure of the carburized layer of each test piece was observed, and the hardness of the carburized layer at a depth of 0.1 mm from the surface layer was measured. The results are shown in Table 3.

【表】 第3表に示すように、この発明による浸炭用鋼
では、カーボンポテンシヤルが1.7%の浸炭雰囲
気中で真空浸炭を施したときでも浸炭層に微細な
球状炭化物が析出しており、浸炭層硬さも十分で
あることが確認され、この発明による浸炭用鋼に
対して過剰浸炭させる場合に真空浸炭を施すこと
も良いことが確かめられた。これに対して比較例
の場合には高温の浸炭処理によつて粗大なネツト
状炭化物が析出し、浸炭層の硬さも低いという好
ましくない結果となつた。 以上説明してきたように、この発明による浸炭
用鋼は、重量%で、C:0.1〜0.3%.、Mn:0.2〜
1.5%、Cr:1〜3%で且つMn+Cr≦3%を含
み、さらに、Si:0.5〜1.5%、Al:0.2〜1.5%、
必要に応じて、Mo:0.1〜0.5%、V:0.1〜0.5
%、Ti:0.1〜0.5%、Zr:0.1〜0.5%、Nb+
Ta:0.1〜0.5%のうちの1種または2種以上を含
有し、残部Feおよび不純物からなり、浸炭処理
後の浸炭層に微細な球状炭化物が析出するもので
あるから、浸炭雰囲気のカーボンポテンシヤルが
2.5%以下程度の通常の浸炭処理を施したときで
も過剰浸炭が可能であり、この過剰浸炭によつて
表面の硬度を著しく高めることが可能であつて、
耐ピツチング性や疲労強度に優れたギヤ、コンロ
ツド、ピンオン、ラツク、ベアリング、ベアリン
グレース、ステアリング部品等の浸炭部品を得る
ことができ、これらの部品が軽量化の要請に基づ
いて小型化されているときでも通常の浸炭処理を
施すことによつて十分優れた強度をもつものとす
ることができ、従来のように過剰浸炭を行うため
に特殊な浸炭処理を施す必要もないなどの著大な
る効果を有するものである。
[Table] As shown in Table 3, in the steel for carburizing according to the present invention, even when vacuum carburizing was performed in a carburizing atmosphere with a carbon potential of 1.7%, fine spherical carbides were precipitated in the carburized layer. It was confirmed that the layer hardness was sufficient, and it was also confirmed that vacuum carburizing can be applied when excessively carburizing the steel for carburizing according to the present invention. On the other hand, in the case of the comparative example, coarse net-like carbides were precipitated by high-temperature carburizing treatment, and the hardness of the carburized layer was also low, which was an unfavorable result. As explained above, the carburizing steel according to the present invention has C: 0.1 to 0.3% by weight. , Mn: 0.2~
1.5%, Cr: 1-3% and contains Mn + Cr≦3%, further Si: 0.5-1.5%, Al: 0.2-1.5%,
Mo: 0.1~0.5%, V: 0.1~0.5 as required
%, Ti: 0.1-0.5%, Zr: 0.1-0.5%, Nb+
Ta: Contains one or more of 0.1 to 0.5%, with the balance consisting of Fe and impurities, and fine spherical carbides precipitate in the carburized layer after carburizing, so the carbon potential of the carburizing atmosphere but
Excessive carburization is possible even when normal carburizing is carried out to a level of 2.5% or less, and this excessive carburization can significantly increase the hardness of the surface.
Carburized parts such as gears, connecting rods, pin-ons, racks, bearings, bearing races, and steering parts with excellent pitting resistance and fatigue strength can be obtained, and these parts are being miniaturized based on the demand for weight reduction. Even in some cases, it is possible to obtain sufficiently excellent strength by applying normal carburizing treatment, and there is a great effect that there is no need to perform special carburizing treatment to perform excessive carburizing as in the past. It has the following.

Claims (1)

【特許請求の範囲】 1 重量%で、C:0.1〜0.3%、Mn:0.2〜1.5
%、Cr:1〜3%で且つMn+Cr≦3%を含み、
さらに、Si:0.5〜1.5%、Al:0.2〜1.5%を含有
し、残部Feおよび不純物からなり、浸炭処理後
の浸炭層に微細な球状炭化物が析出することを特
徴とする浸炭用鋼。 2 重量%で、C:0.1〜0.3%、Mn:0.2〜1.5
%、Cr:1〜3%で且つMn+Cr≦3%を含み、
さらに、Si:0.5〜1.5%、Al:0.2〜1.5%を含有
し、さらにまたMo:0.1〜0.5%、V:0.1〜0.5
%、Ti:0.1〜0.5%、Zr:0.1〜0.5%、Nb+
Ta:0.1〜0.5%のうちの1種または2種以上を含
有し、残部Feおよび不純物からなり、浸炭処理
後の浸炭層に微細な球状炭化物が析出することを
特徴とする浸炭用鋼。
[Claims] 1% by weight, C: 0.1-0.3%, Mn: 0.2-1.5
%, Cr: 1 to 3% and includes Mn + Cr≦3%,
Further, a carburizing steel containing 0.5 to 1.5% of Si and 0.2 to 1.5% of Al, with the remainder consisting of Fe and impurities, and fine spherical carbides precipitate in the carburized layer after carburizing. 2 In weight%, C: 0.1-0.3%, Mn: 0.2-1.5
%, Cr: 1 to 3% and includes Mn + Cr≦3%,
Furthermore, it contains Si: 0.5 to 1.5%, Al: 0.2 to 1.5%, Mo: 0.1 to 0.5%, and V: 0.1 to 0.5.
%, Ti: 0.1-0.5%, Zr: 0.1-0.5%, Nb+
A carburizing steel containing one or more of Ta: 0.1 to 0.5%, the remainder consisting of Fe and impurities, and fine spherical carbides precipitate in the carburized layer after carburizing.
JP10427783A 1983-06-13 1983-06-13 Carburizing steel Granted JPS59232252A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP10427783A JPS59232252A (en) 1983-06-13 1983-06-13 Carburizing steel

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP10427783A JPS59232252A (en) 1983-06-13 1983-06-13 Carburizing steel

Publications (2)

Publication Number Publication Date
JPS59232252A JPS59232252A (en) 1984-12-27
JPH0454736B2 true JPH0454736B2 (en) 1992-09-01

Family

ID=14376427

Family Applications (1)

Application Number Title Priority Date Filing Date
JP10427783A Granted JPS59232252A (en) 1983-06-13 1983-06-13 Carburizing steel

Country Status (1)

Country Link
JP (1) JPS59232252A (en)

Families Citing this family (6)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS6033338A (en) * 1983-08-02 1985-02-20 Nissan Motor Co Ltd Steel to be carburized
JPS61210154A (en) * 1985-03-13 1986-09-18 Kobe Steel Ltd Low strain carburizing steel
JPH0672280B2 (en) * 1985-06-25 1994-09-14 日産自動車株式会社 High toughness carburizing steel
JP2503400B2 (en) * 1985-10-17 1996-06-05 大同特殊鋼株式会社 Manufacturing method of carburized parts
US5085733A (en) * 1989-08-24 1992-02-04 Nippon Seiko Kabushiki Kaisha Rolling steel bearing
JP5683348B2 (en) * 2011-03-29 2015-03-11 愛知製鋼株式会社 Carburized member, steel for carburized member, and method for manufacturing carburized member

Family Cites Families (7)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS53147616A (en) * 1977-05-31 1978-12-22 Nippon Steel Corp Case hardening steel
JPS5475419A (en) * 1977-11-29 1979-06-16 Komatsu Mfg Co Ltd Wear resistant steel for cementation
JPS54145334A (en) * 1978-05-02 1979-11-13 Daido Steel Co Ltd Cemented* caseehardened steel for use as gear
JPS5948949B2 (en) * 1978-12-27 1984-11-29 愛知製鋼株式会社 carburizing steel
JPS55161065A (en) * 1979-05-22 1980-12-15 Daido Steel Co Ltd Manufacture of mission synchro mechanism parts having least strain
JPS5675551A (en) * 1979-11-22 1981-06-22 Sanyo Tokushu Seikou Kk Grain stabilized carburizing steel
JPS57104625A (en) * 1980-12-19 1982-06-29 Sumitomo Metal Ind Ltd Manufacture of fine-grain case-hardening steel

Also Published As

Publication number Publication date
JPS59232252A (en) 1984-12-27

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