JPH086169B2 - Gas carburizing method for steel parts - Google Patents
Gas carburizing method for steel partsInfo
- Publication number
- JPH086169B2 JPH086169B2 JP3192521A JP19252191A JPH086169B2 JP H086169 B2 JPH086169 B2 JP H086169B2 JP 3192521 A JP3192521 A JP 3192521A JP 19252191 A JP19252191 A JP 19252191A JP H086169 B2 JPH086169 B2 JP H086169B2
- Authority
- JP
- Japan
- Prior art keywords
- temperature
- carburizing
- gas
- rate
- carbon
- 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
Links
- 238000005255 carburizing Methods 0.000 title claims description 70
- 238000000034 method Methods 0.000 title claims description 25
- 229910000831 Steel Inorganic materials 0.000 title claims description 17
- 239000010959 steel Substances 0.000 title claims description 17
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 claims description 25
- 229910052799 carbon Inorganic materials 0.000 claims description 24
- 238000001816 cooling Methods 0.000 claims description 18
- 230000001351 cycling effect Effects 0.000 claims description 9
- 229910001566 austenite Inorganic materials 0.000 claims description 8
- 239000007789 gas Substances 0.000 description 26
- 230000003647 oxidation Effects 0.000 description 17
- 238000007254 oxidation reaction Methods 0.000 description 17
- 239000002344 surface layer Substances 0.000 description 15
- 239000000463 material Substances 0.000 description 14
- 229910001567 cementite Inorganic materials 0.000 description 12
- KSOKAHYVTMZFBJ-UHFFFAOYSA-N iron;methane Chemical compound C.[Fe].[Fe].[Fe] KSOKAHYVTMZFBJ-UHFFFAOYSA-N 0.000 description 12
- 239000010410 layer Substances 0.000 description 10
- 230000002159 abnormal effect Effects 0.000 description 9
- 230000003179 granulation Effects 0.000 description 9
- 238000005469 granulation Methods 0.000 description 9
- ATUOYWHBWRKTHZ-UHFFFAOYSA-N Propane Chemical compound CCC ATUOYWHBWRKTHZ-UHFFFAOYSA-N 0.000 description 6
- 229910052804 chromium Inorganic materials 0.000 description 5
- 230000000052 comparative effect Effects 0.000 description 5
- 230000015572 biosynthetic process Effects 0.000 description 4
- 238000009792 diffusion process Methods 0.000 description 4
- 239000011159 matrix material Substances 0.000 description 4
- 238000010791 quenching Methods 0.000 description 4
- 230000000171 quenching effect Effects 0.000 description 4
- 230000000694 effects Effects 0.000 description 3
- 239000001294 propane Substances 0.000 description 3
- 238000005204 segregation Methods 0.000 description 3
- 229910045601 alloy Inorganic materials 0.000 description 2
- 239000000956 alloy Substances 0.000 description 2
- 150000001721 carbon Chemical class 0.000 description 2
- 238000007796 conventional method Methods 0.000 description 2
- 238000010438 heat treatment Methods 0.000 description 2
- 229920006395 saturated elastomer Polymers 0.000 description 2
- QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical compound [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 description 1
- 238000005422 blasting Methods 0.000 description 1
- 238000003763 carbonization Methods 0.000 description 1
- 239000013078 crystal Substances 0.000 description 1
- 230000002950 deficient Effects 0.000 description 1
- 238000010586 diagram Methods 0.000 description 1
- 239000006185 dispersion Substances 0.000 description 1
- 238000009826 distribution Methods 0.000 description 1
- 238000013467 fragmentation Methods 0.000 description 1
- 238000006062 fragmentation reaction Methods 0.000 description 1
- 230000001771 impaired effect Effects 0.000 description 1
- 229910000734 martensite Inorganic materials 0.000 description 1
- 238000001000 micrograph Methods 0.000 description 1
- 239000000203 mixture Substances 0.000 description 1
- 229910052750 molybdenum Inorganic materials 0.000 description 1
- 229910052760 oxygen Inorganic materials 0.000 description 1
- 239000001301 oxygen Substances 0.000 description 1
- 239000002244 precipitate Substances 0.000 description 1
- 230000002265 prevention Effects 0.000 description 1
- 230000001737 promoting effect Effects 0.000 description 1
- 238000003303 reheating Methods 0.000 description 1
- 230000000630 rising effect Effects 0.000 description 1
- 238000004904 shortening Methods 0.000 description 1
- 239000006104 solid solution Substances 0.000 description 1
- 230000006641 stabilisation Effects 0.000 description 1
- 238000011105 stabilization Methods 0.000 description 1
- 229910000859 α-Fe Inorganic materials 0.000 description 1
Landscapes
- Solid-Phase Diffusion Into Metallic Material Surfaces (AREA)
Description
【0001】[0001]
【産業上の利用分野】本発明は鋼材部品のガス浸炭法、
特に、雰囲気中のカーボンポテンシャルをAcm、即ち、
浸炭温度におけるオーステナイト中の炭素の飽和濃度と
の平衡値以上に維持しながら、被処理物をガス浸炭する
高濃度ガス浸炭方法に関する。The present invention relates to a gas carburizing method for steel parts,
Especially, the carbon potential in the atmosphere is Acm, that is,
The present invention relates to a high-concentration gas carburizing method for gas carburizing an object to be treated while maintaining the equilibrium value with the saturation concentration of carbon in austenite at the carburizing temperature.
【0002】[0002]
【従来の技術】従来、自動車部品、機械部品その他の鋼
材部品の耐摩耗性、耐ピッチング性等を向上させる手段
として、ガス浸炭法、特に、高濃度ガス浸炭法が採用さ
れている。この高濃度ガス浸炭法は、基本的には、浸炭
性ガスを炉内に供給し、その雰囲気中のカーボンポテン
シャルをAcm以上に維持しながら、被処理物をオーステ
ナイト温度域内の一定温度で加熱することによって、そ
の表面に炭素を吸収させ、マトリックスに第2相である
炭化物を分散析出させる方法である。2. Description of the Related Art Conventionally, a gas carburizing method, particularly a high-concentration gas carburizing method, has been adopted as a means for improving the wear resistance and pitting resistance of automobile parts, machine parts and other steel parts. In this high-concentration gas carburizing method, basically, a carburizing gas is supplied into the furnace, and the object to be processed is heated at a constant temperature within the austenite temperature range while maintaining the carbon potential in the atmosphere at Acm or higher. In this way, carbon is absorbed on the surface and the second phase carbide is dispersed and precipitated in the matrix.
【0003】この高濃度ガス浸炭法として、例えば、
(イ)一定温度で高濃度ガス浸炭処理を行った後、室温
まで空冷し、これを再度所定温度まで急速加熱した後、
直ちに急冷焼入れする方法(特公昭47ー32182号
公報)、(ロ)Acm以下のカーボンポテンシャルで予備
浸炭し、これを再加熱してAcmを越えるカーボンポテン
シャルで浸炭処理した後、焼入れする方法(特公昭62
ー24499号公報)、及び(ハ)雰囲気中のカーボン
ポテンシャルがAcm以下の条件下で一次浸炭処理した
後、空気中で冷却し表面の粒界酸化層を酸化させ、その
粒界酸化層をショットブラストで除去した後、雰囲気中
のカーボンポテンシャルがAcmを越える条件下で2次浸
炭する方法(特公昭63ー60113号公報)など種々
の方法が提案されている。As this high-concentration gas carburizing method, for example,
(A) After performing a high-concentration gas carburizing process at a constant temperature, air-cooling to room temperature, and then rapidly heating it to a predetermined temperature again,
Immediately quenching and quenching (Japanese Patent Publication No. Sho 47-32182), (b) Pre-carburizing with a carbon potential of Acm or less, reheating and carburizing with a carbon potential of more than Acm, and then quenching (special Kosho 62
No. 24499 gazette) and (c) After the primary carburizing treatment under the condition that the carbon potential in the atmosphere is A cm or less, the grain boundary oxide layer on the surface is oxidized by cooling in air and the grain boundary oxide layer is shot. Various methods have been proposed, such as a method of secondary carburization under conditions where the carbon potential in the atmosphere exceeds Acm after removal by blasting (Japanese Patent Publication No. 63-60113).
【0004】[0004]
【発明が解決しようとする課題】しかしながら、従来の
高濃度ガス浸炭方法では、いずれも浸炭温度を一定にし
て浸炭を行っているため、浸炭時間の経過と共に被処理
物中の一部の合金元素、例えば、Cr,Si,Mnなど
が選択的に酸化されて表層および表層近傍の粒界に集中
し、数10μの粒界酸化および浸炭異常層を生じ、十分
な焼入硬度が得られなくなるという問題がある。しか
も、粒界酸化が生じると、その近傍のCr,Mnなどが
欠乏してセメンタイトを形成し難くなり、また炭素濃度
も上がらず、浸炭むらを生じ、このため、耐摩耗性、耐
ピッチング性などの機械的性質が低下し、材料本来の特
性が損なわれるという問題がある。さらに、セメンタイ
トの粒状化、特に、表層より約0.1mm以上の深さでの
粒状化が不十分となり易いという問題がある。However, in all of the conventional high-concentration gas carburizing methods, carburizing is carried out at a constant carburizing temperature. For example, Cr, Si, Mn, etc. are selectively oxidized and concentrated on the surface layer and the grain boundaries in the vicinity of the surface layer, resulting in grain boundary oxidation of several tens of μ and an abnormal carburization layer, which makes it impossible to obtain sufficient quenching hardness. There's a problem. Moreover, when grain boundary oxidation occurs, Cr and Mn in the vicinity are deficient and it becomes difficult to form cementite. Further, the carbon concentration does not increase and carburizing unevenness occurs, which results in wear resistance, pitting resistance, etc. However, there is a problem in that the mechanical properties of the material deteriorate and the original characteristics of the material are impaired. Further, there is a problem that the granulation of cementite, particularly the granulation at a depth of about 0.1 mm or more from the surface layer, tends to be insufficient.
【0005】従って、本発明は、高濃度ガス浸炭処理時
の粒界酸化及び浸炭異常層の形成を抑制し、表層に微細
な粒状セメンタイトを高密度に生成させ、耐摩耗性、耐
ピッチング性などの機械的性質を向上させることを主目
的とするものである。Therefore, the present invention suppresses the grain boundary oxidation and the formation of the abnormal carburization layer at the time of high-concentration gas carburizing treatment, and produces fine granular cementite at a high density in the surface layer, resulting in wear resistance, pitting resistance, etc. Its main purpose is to improve the mechanical properties of.
【0006】[0006]
【課題を解決するための手段】本発明は、前記課題を解
決するための手段として、鋼材部品をAcm以上のカーボ
ンポテンシャルの雰囲気中でガス浸炭処理するに際し、
オーステナイト温度域で浸炭温度を10〜50℃、好ま
しくは20〜30℃の範囲でサイクリングさせるように
したものであって、要すれば、オーステナイト温度域で
浸炭温度を前記温度範囲内でサイクリングさせると共
に、浸炭途中でAr1点以下の所定温度まで冷却するよ
うにしたものである。[Means for Solving the Problems] As a means for solving the above problems, the present invention provides a gas carburizing process for steel parts in an atmosphere having a carbon potential of A cm or more,
The carburizing temperature is cycled in the austenite temperature range of 10 to 50 ° C., preferably 20 to 30 ° C. If necessary, the carburizing temperature is cycled in the austenite temperature range within the temperature range. In the middle of carburizing, the material is cooled to a predetermined temperature of Ar 1 point or less.
【0007】本発明に係る高濃度ガス浸炭法は、浸炭温
度をオーステナイト温度域内の所定温度とその温度より
も10〜50℃高い若しくは低い温度とに周期的に変
え、被処理物をこれらの各温度で交互に所定時間処理す
ることによって行われるが、この浸炭温度をサイクリン
グさせる周期は、通常、10分〜180分/サイクルの
範囲で設定される。炉が通常のバッチ炉の場合は、操業
性を考慮して60分/サイクル程度に設定するのが好ま
しい。なお、被処理物である鋼材部品の材質は必ずしも
浸炭鋼である必要はなく、汎用鋼であっても良い。In the high-concentration gas carburizing method according to the present invention, the carburizing temperature is cyclically changed to a predetermined temperature within the austenite temperature range and a temperature which is 10 to 50 ° C. higher or lower than the temperature, and the object to be treated is subjected to each of these. The carburizing temperature is cycled by alternately treating at a temperature for a predetermined time, and the cycle of cycling the carburizing temperature is usually set in the range of 10 minutes to 180 minutes / cycle. When the furnace is an ordinary batch furnace, it is preferable to set it to about 60 minutes / cycle in consideration of operability. The material of the steel part that is the object to be treated does not necessarily have to be carburized steel, but may be general purpose steel.
【0008】また、サイクリング時の冷却は、理論的に
は急冷がよいが、実用炉での一般的な炉冷速度0.5〜
2℃/min 程度で十分な効果が得られる。また、サイク
リング時の昇温は、理論的には冷却時とは逆にゆっくり
としたほうが良いが、現実的には1℃/min 以下で良
い。これは、急熱しすぎると材料表層のマトリックス中
の炭素が不飽和になるからである。[0008] In addition, although the rapid cooling is theoretically preferable for cooling during cycling, a general furnace cooling rate in a practical furnace is 0.5-0.5.
A sufficient effect can be obtained at about 2 ° C / min. Further, theoretically, it is better that the temperature rise during cycling is slower than that during cooling, but in reality, it may be 1 ° C./min or less. This is because the carbon in the matrix of the material surface layer becomes unsaturated when it is heated too quickly.
【0009】本発明の実施態様においては、浸炭処理の
途中でAr1点以下の所定温度まで少なくとも一回冷却
されるが、この場合の温度はAr1点以下Ms点以上の
温度範囲内の温度が良く、通常、300〜730℃、好
ましくは400〜500℃の範囲内の温度に設定され
る。また、その時の冷却速度は、過剰のフェライトが生
じたり、マルテンサイトが生成しない程度の速度が良
く、通常、3〜60℃/minに設定される。また、冷却
後の昇温速度は、冷却速度よりの遅い速度、通常、1〜
15℃/minに設定するのが好ましい。In the embodiment of the present invention, the carburizing process is cooled at least once to a predetermined temperature of Ar 1 point or lower. In this case, the temperature is within a temperature range of Ar 1 point or lower and Ms point or higher. The temperature is usually 300 to 730 ° C., preferably 400 to 500 ° C. Further, the cooling rate at that time is good enough to prevent excessive ferrite from being generated or martensite to be generated, and is usually set to 3 to 60 ° C./min. The rate of temperature increase after cooling is slower than the cooling rate, usually 1 to
It is preferably set to 15 ° C / min.
【0010】[0010]
【作用】吸熱型雰囲気中でAcm以上のカーボンポテンシ
ャルで浸炭処理を行う、いわゆる飽和値浸炭を行うと、
被処理物の表層部に炭素が吸収、拡散され、表面炭素濃
度が高められるが、浸炭中に、浸炭温度を10〜50℃
の温度範囲内でサイクリングさせると、浸炭温度の降下
時に被処理物の表層部ではマトリックス中の炭素が過飽
和となってセメンタイトが分散析出すると共に、炭素が
雰囲気中へ放出される。このようにオーステナイト中に
固溶している炭素がセメンタイトとして析出する際に生
成される活性炭素が被処理物表層部の酸化物と反応し
て、その酸化物を還元し酸素分を材料外へ駆逐すると共
に、還元されたCr,Mnなどの合金元素は再びマトリ
ックス中へ拡散する。選択的に酸化され易い合金元素の
うちSiは一度酸化すると還元されないが、Cr,Mn
等は還元されるため粒界酸化が減少し、浸炭異常層の生
成が抑制される。[Operation] Carburizing in the endothermic atmosphere with a carbon potential of Acm or more, that is, when performing so-called saturation value carburizing,
Carbon is absorbed and diffused in the surface layer of the object to be treated, and the surface carbon concentration is increased, but the carburizing temperature is 10 to 50 ° C during carburizing.
When the carbonization temperature is lowered, carbon in the matrix becomes supersaturated in the surface layer portion of the object to be treated, cementite is dispersed and precipitated, and carbon is released into the atmosphere when the temperature is lowered. In this way, the activated carbon generated when the solid solution carbon in austenite precipitates as cementite reacts with the oxide of the surface layer of the object to be processed, reduces the oxide and removes the oxygen content from the material. As the alloy elements such as Cr and Mn are expelled, they are diffused into the matrix again. Among alloy elements that are easily oxidized selectively, Si is not reduced once oxidized, but Cr, Mn
Etc. are reduced, the grain boundary oxidation is reduced and the generation of the abnormal carburized layer is suppressed.
【0011】浸炭温度のサイクリングの温度幅を10〜
50℃、好ましくは20〜30℃としたのは、次の理由
による。即ち、ガス浸炭処理における浸炭時間(t)と
浸炭深さ(d)は、式:d=k√t(mm)で与えられ、
ある温度に於けるγFe中の飽和炭素量および炭素の拡
散係数は、表1に示されるように、温度が上昇する程増
大する。従って、サイクリングの温度幅が大きいほど飽
和炭素量の差が大きくなり粒界酸化を軽減させることが
できるが、拡散速度の差が大きくなり浸炭時間の短縮化
を図る上で効果的ではなく、また、高温部に比べ低温部
の温度が低すぎると、還元速度より酸化速度が大きくな
り粒界酸化を軽減できないので前記範囲とした。The temperature range of carburizing temperature cycling is 10
The reason why the temperature is 50 ° C., preferably 20 to 30 ° C. is as follows. That is, the carburizing time (t) and carburizing depth (d) in the gas carburizing process are given by the equation: d = k√t (mm),
As shown in Table 1, the saturated carbon amount and the carbon diffusion coefficient in γFe at a certain temperature increase as the temperature increases. Therefore, the larger the temperature range of cycling is, the larger the difference in the saturated carbon amount is, which can reduce the grain boundary oxidation, but the difference in the diffusion rate is large, which is not effective in shortening the carburizing time. If the temperature of the low temperature portion is too low compared to the high temperature portion, the oxidation rate becomes higher than the reduction rate and the grain boundary oxidation cannot be reduced, so the above range was set.
【0012】[0012]
【表1】 γFe中の飽和C量、Cの拡散係数 飽和C量 Cの拡散係数(k) 930℃ 1.3% 0.63 900℃ 1.2% 0.54 870℃ 1.1% 0.44 [Table 1] Saturated C amount in γFe, diffusion coefficient of C Saturated C amount Diffusion coefficient of C (k) 930 ° C 1.3% 0.63 900 ° C 1.2% 0.54 870 ° C 1.1% 0 .44
【0013】また、浸炭処理の途中で、一回以上Ar1
点以下Ms点以上の温度にまで冷却すると、結晶粒内に
細かい多数のセメンタイト核が析出し、これをAc1点
以上にゆっくりと昇温させると、セメンタイトの安定化
及び粒状化が促進される。この中間冷却はセメンタイト
の粒状化、特に、内部の粒状化に寄与する。During the carburizing process, Ar 1
When cooled to a temperature equal to or lower than the Ms point and below, a large number of fine cementite nuclei are precipitated in the crystal grains, and when the temperature is slowly raised to the Ac 1 point or higher, stabilization and granulation of the cementite are promoted. . This intermediate cooling contributes to the granulation of cementite, especially to the granulation of the inside.
【0014】更に、前記中間冷却後の浸炭処理での浸炭
温度のサイクリングは、粒界酸化の軽減のみならず粒状
化の促進にも寄与し、とくに表層より少し内部に入った
部分の粒界のセメンタイトの分断、粒状化および粒界近
傍に生成する異常組織の発生防止に効果がある。もとも
と中間の冷却は粒状化の促進が目的であるが、温度のサ
イクリングはさらにその効果を助長する役割を果す。Further, the cycling of the carburizing temperature in the carburizing treatment after the intermediate cooling contributes not only to the reduction of grain boundary oxidation but also to the promotion of granulation. Particularly, the grain boundary of a portion slightly inside the surface layer It is effective for fragmentation of cementite, granulation, and prevention of the generation of abnormal structures near grain boundaries. Originally, the purpose of intermediate cooling is to promote granulation, but temperature cycling plays a role of further promoting the effect.
【0015】次に、本発明の実施例について説明するNext, an embodiment of the present invention will be described.
【0016】[0016]
【実施例】(実施例1)0.1%C、0.3%Si、0.
6%Mn、2.6%Cr、0.4%Mo、残部実質的にF
eからなる浸炭鋼を被処理材とし、これを装填した浸炭
炉に、吸熱型ガス(20%CO,40%H2,40%
N2)1m3/hにプロパンガスを0.8〜1.2%加えた浸
炭性ガスを供給し、図1に示すように、初めに雰囲気温
度を30℃/minの速度で850℃に昇温させた後、1
℃/minの昇温速度で880℃まで昇温させ、その温度
で30分間保持した後、1℃/minの速度で900℃に
昇温させてその温度で10分間保持し、次いで2℃/mi
nの速度で880℃まで降温させて20分間保持し、以
後は、30分毎に昇温−保持と降温−保持の操作を交互
に繰り返して25時間浸炭処理し、次いで、10〜12
℃/minの降温速度で400〜500℃まで冷却したの
ち常温まで冷却して試料を得た。なお、浸炭処理中、雰
囲気中のカーボンポテンシャルは1.4〜1.5(計算
値)に維持した。EXAMPLES (Example 1) 0.1% C, 0.3% Si, 0.1%
6% Mn, 2.6% Cr, 0.4% Mo, balance substantially F
A carburized steel consisting of e was used as a material to be treated, and a carburizing furnace loaded with the material was put into an endothermic gas (20% CO, 40% H 2 , 40%
A carburizing gas obtained by adding 0.8 to 1.2% of propane gas to N 2 ) 1 m 3 / h was supplied, and as shown in FIG. 1, the ambient temperature was initially set to 850 ° C. at a rate of 30 ° C./min. After raising the temperature, 1
The temperature is raised to 880 ° C at a rate of ℃ / min, held at that temperature for 30 minutes, then raised to 900 ° C at a rate of 1 ° C / min and held at that temperature for 10 minutes, and then at 2 ° C / min. mi
The temperature was lowered to 880 ° C. at a rate of n and held for 20 minutes, and thereafter, every 30 minutes, the operation of temperature increase-holding and temperature decrease-holding was alternately repeated to perform carburizing treatment for 25 hours, and then 10 to 12
A sample was obtained by cooling to 400 to 500 ° C. at a temperature lowering rate of ° C./min and then to room temperature. During the carburizing process, the carbon potential in the atmosphere was maintained at 1.4 to 1.5 (calculated value).
【0017】(実施例2) SCR−415を被処理材
とし、これを装填した浸炭炉に実施例1のものと同組成
の浸炭性ガスを供給し、図2に示すように、初めに雰囲
気温度を30℃/minの速度で850℃まで昇温させた
後、1℃/minの昇温速度で880℃に昇温させ、その
温度で30分間保持した後、1℃/minの速度で900
℃に昇温させてその温度で10分間保持し、次いで2℃
/minの速度で880℃まで降温させて20分間保持
し、以後は、30分毎に昇温−保持と降温−保持の操作
を交互に繰り返して15時間浸炭処理し、次いで10〜
12℃/minの降温速度で400〜500℃にまで一旦
冷却し、直ちに20〜24℃/minの昇温速度でもとの
浸炭温度880℃にまで昇温させ、さらに前記条件で3
0分毎に昇温−保持と降温−保持の操作を交互に繰り返
して10時間浸炭処理し、次いで10〜12℃/minの
降温速度で400〜500℃まで冷却したのち常温まで
冷却して試料を得た。浸炭処理中、雰囲気のカーボンポ
テンシャルは、実施例1と同様に、浸炭性ガス中のプロ
パンガスの濃度を調節して1.4〜1.55(計算値)に
維持した。(Example 2) A carburizing gas having the same composition as in Example 1 was supplied to a carburizing furnace loaded with SCR-415 as a material to be treated, and as shown in FIG. The temperature was raised to 850 ° C at a rate of 30 ° C / min, then raised to 880 ° C at a rate of 1 ° C / min, held at that temperature for 30 minutes, and then at a rate of 1 ° C / min. 900
Up to ℃ and hold at that temperature for 10 minutes, then 2 ℃
The temperature was lowered to 880 ° C. at a rate of / min and held for 20 minutes. Thereafter, every 30 minutes, a temperature raising-holding operation and a temperature lowering-holding operation were alternately repeated to perform a carburizing treatment for 15 hours.
It is once cooled to 400 to 500 ° C. at a temperature lowering rate of 12 ° C./min, and immediately heated to the original carburizing temperature of 880 ° C. at a temperature raising rate of 20 to 24 ° C./min.
Carrying treatment is repeated for 10 hours by alternately repeating temperature increasing-holding and temperature decreasing-holding every 0 minutes, then cooling to 400 to 500 ° C at a temperature lowering rate of 10 to 12 ° C / min, and then cooling to room temperature to obtain a sample. Got During the carburizing treatment, the carbon potential of the atmosphere was maintained at 1.4 to 1.55 (calculated value) by adjusting the concentration of propane gas in the carburizing gas as in Example 1.
【0018】(比較例) 実施例1で用いた浸炭鋼と同
じ浸炭鋼を被処理材として用い、これを装填した浸炭炉
に吸熱型ガス(20%CO,40%H2,40%N2)1
m3/hにプロパンガスを0.5〜0.7%加えた浸炭性ガス
を供給し、図3に示すように、初めに雰囲気温度を30
℃/minの速度で850℃まで昇温させた後、1℃/min
の昇温速度で890℃に昇温させ、その温度で25時間
浸炭処理し、次いで10〜12℃/minの降温速度で4
00〜500℃まで冷却したのち、常温まで冷却して試
料を得た。浸炭処理中、雰囲気中のカーボンポテンシャ
ルは1.4〜1.5(計算値)に維持した。Comparative Example The same carburized steel as the carburized steel used in Example 1 was used as a material to be treated, and a carburizing furnace loaded with the same had endothermic gas (20% CO, 40% H 2 , 40% N 2). ) 1
A carburizing gas obtained by adding 0.5 to 0.7% of propane gas to m 3 / h was supplied, and as shown in FIG.
1 ℃ / min after heating up to 850 ℃ at a speed of ℃ / min
At a temperature rising rate of 890 ° C., carburizing at that temperature for 25 hours, and then at a temperature lowering rate of 10 to 12 ° C./min for 4 hours.
After cooling to 00 to 500 ° C., it was cooled to room temperature to obtain a sample. During the carburizing process, the carbon potential in the atmosphere was maintained at 1.4 to 1.5 (calculated value).
【0019】実施例1、2および比較例で得た各試料を
850℃に再加熱した後、焼入れを行い、それらの表面
近傍のマクロ組織を示す顕微鏡写真をそれぞれ図4、
5、6に示す。図4(a)は実施例1で得た高濃度浸炭
鋼の焼入組織を、同図(b)はその表層の粒界酸化をそ
れぞれ示し、図5(a)は実施例2で得た試料の焼入組
織を、同図(b)はその表層の粒界酸化を、図6(a)
は比較例で得た試料の焼入組織を、同図(b)はその表
層の粒界酸化をそれぞれ示す。The samples obtained in Examples 1 and 2 and Comparative Example were reheated to 850 ° C. and then quenched, and micrographs showing macrostructures near their surfaces are shown in FIG. 4 and FIG.
5 and 6 are shown. 4 (a) shows the quenched structure of the high-concentration carburized steel obtained in Example 1, FIG. 4 (b) shows the grain boundary oxidation of the surface layer, and FIG. 5 (a) was obtained in Example 2. Fig. 6 (a) shows the quenched structure of the sample, Fig. 6 (b) shows the grain boundary oxidation of the surface layer,
Shows the quenched structure of the sample obtained in the comparative example, and FIG. 6B shows the grain boundary oxidation of the surface layer.
【0020】図6(a)から明らかなように、比較例の
ものでは、浸炭異常層(表層の黒い部分)が最大約50
μmの深さまで生じ、内部にも粒界に沿って偏析が認め
られ、セメンタイト(白い球状のもの)の分散状態も不
均一である。また、同図(b)から、比較例のものは粒
界酸化(表層のひげ状の部分)が50μm程度の深さま
で生じていることが解る。As is clear from FIG. 6 (a), in the comparative example, the abnormal carburization layer (black portion of the surface layer) is about 50 at maximum.
It occurs up to a depth of μm, segregation is also observed along the grain boundaries inside, and the dispersion state of cementite (white sphere) is also non-uniform. Further, from FIG. 6B, it is understood that in the comparative example, grain boundary oxidation (whisker-like portion of the surface layer) occurs up to a depth of about 50 μm.
【0021】これに対して、実施例1のものでは、図4
(a)から解るように、浸炭異常層は20μm程度に減
少し、粒界に沿った偏析も軽減しており、また同図
(b)から明らかなように、粒界酸化深さもその発生分
布も少ない。また、実施例2のものでは、図5(a)か
ら明らかなように、表層には微細なセメンタイトが密に
形成され、浸炭異常層の生成が全く認められないだけで
なく、内部まで粒状化され分散も良く組織網に沿った偏
析も認められず、また、同図(b)から明らかなよう
に、粒界酸化も殆どない。On the other hand, in the first embodiment, as shown in FIG.
As can be seen from (a), the abnormal carburized layer is reduced to about 20 μm, and segregation along the grain boundaries is also reduced. Also, as is clear from (b) in the figure, the grain boundary oxidation depth and the occurrence distribution are also shown. Also few. In addition, in Example 2, as is clear from FIG. 5 (a), fine cementite is densely formed in the surface layer, and not only the formation of the abnormal carburized layer is not observed but also the inside is granulated. As a result, segregation along the texture network was not observed, and there was almost no grain boundary oxidation, as is clear from FIG.
【0022】[0022]
【発明の効果】以上の説明から明らかなように、本発明
は、通常浸炭に比べて粒界酸化の少ない飽和値浸炭法を
採用し、その浸炭処理時に浸炭温度を所定範囲内でサイ
クリングさせることにより、粒界酸化及び浸炭異常層の
生成を防止することができる。また、浸炭温度のサイク
リングと共に、その途中でAr1以下に冷却することに
より粒界酸化および浸炭異常層の生成をほとんど無くす
ることができ、しかも、内部の粒状化の促進化を図り微
細なセメンタイトを密に形成させることができ、従っ
て、鋼材部品の耐摩耗性、耐ピッチング性などの機械的
性質を向上させることができるという優れた効果を奏す
る。As is apparent from the above description, the present invention employs a saturation value carburizing method that causes less intergranular oxidation than ordinary carburizing, and the carburizing temperature is cycled within a predetermined range during the carburizing treatment. This makes it possible to prevent the grain boundary oxidation and the formation of the abnormal carburizing layer. By cooling the carburizing temperature to below Ar 1 along with cycling of the carburizing temperature, it is possible to almost eliminate grain boundary oxidation and formation of an abnormal carburized layer, and further promote the internal granulation to obtain fine cementite. Can be densely formed, and therefore, an excellent effect that mechanical properties such as wear resistance and pitting resistance of the steel material component can be improved is exhibited.
【図1】 本発明方法の一実施例を示すヒートサイクル
の説明図である。FIG. 1 is an explanatory view of a heat cycle showing an embodiment of the method of the present invention.
【図2】 本発明方法の他の実施例を示すヒートサイク
ルの説明図である。FIG. 2 is an explanatory view of a heat cycle showing another embodiment of the method of the present invention.
【図3】 従来法のヒートサイクルの説明図である。FIG. 3 is an explanatory diagram of a heat cycle of a conventional method.
【図4】 本発明方法の第1実施例によりガス浸炭処理
した鋼材の金属組織を示す写真である。FIG. 4 is a photograph showing a metallographic structure of a steel material subjected to gas carburizing treatment according to the first embodiment of the method of the present invention.
【図5】 本発明方法の第2実施例によりガス浸炭処理
した鋼材の金属組織を示す写真である。FIG. 5 is a photograph showing a metallographic structure of a steel material subjected to a gas carburizing treatment according to a second embodiment of the method of the present invention.
【図6】 従来法によりガス浸炭処理した鋼材の金属組
織を示す写真である。FIG. 6 is a photograph showing the metallographic structure of a steel material that has been gas carburized by a conventional method.
Claims (2)
気中でガス浸炭処理を行うに際し、オーステナイト温度
域で浸炭温度を10〜50℃の範囲でサイクリングさせ
ることを特徴とする鋼材部品のガス浸炭方法。1. A gas carburizing method for steel parts, which comprises cycling the carburizing temperature in the range of 10 to 50 ° C. in the austenite temperature range when performing the gas carburizing treatment in an atmosphere having a carbon potential of A cm or more.
気中でガス浸炭処理を行うに際し、オーステナイト温度
域で浸炭温度を10〜50℃の範囲でサイクリングさせ
ると共に、浸炭途中でAr1点以下の所定温度まで冷却
することを特徴とする鋼材部品のガス浸炭方法。2. When carrying out a gas carburizing treatment in an atmosphere having a carbon potential of A cm or more, the carburizing temperature is cycled within the range of 10 to 50 ° C. in the austenite temperature range, and a predetermined temperature of Ar 1 point or less is reached during carburizing. A gas carburizing method for steel parts, characterized by cooling.
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP3192521A JPH086169B2 (en) | 1991-07-06 | 1991-07-06 | Gas carburizing method for steel parts |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP3192521A JPH086169B2 (en) | 1991-07-06 | 1991-07-06 | Gas carburizing method for steel parts |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| JPH0598417A JPH0598417A (en) | 1993-04-20 |
| JPH086169B2 true JPH086169B2 (en) | 1996-01-24 |
Family
ID=16292673
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP3192521A Expired - Lifetime JPH086169B2 (en) | 1991-07-06 | 1991-07-06 | Gas carburizing method for steel parts |
Country Status (1)
| Country | Link |
|---|---|
| JP (1) | JPH086169B2 (en) |
Families Citing this family (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| CH688801A5 (en) * | 1994-07-07 | 1998-03-31 | Solo Fours Ind Sa | A method of carburizing and carbonitriding steels. |
Family Cites Families (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JPH02294462A (en) * | 1989-05-10 | 1990-12-05 | Mazda Motor Corp | Carburizing quenching method for steel member |
-
1991
- 1991-07-06 JP JP3192521A patent/JPH086169B2/en not_active Expired - Lifetime
Also Published As
| Publication number | Publication date |
|---|---|
| JPH0598417A (en) | 1993-04-20 |
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