JP5760453B2 - Carburized material - Google Patents
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- JP5760453B2 JP5760453B2 JP2011014295A JP2011014295A JP5760453B2 JP 5760453 B2 JP5760453 B2 JP 5760453B2 JP 2011014295 A JP2011014295 A JP 2011014295A JP 2011014295 A JP2011014295 A JP 2011014295A JP 5760453 B2 JP5760453 B2 JP 5760453B2
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- 239000000463 material Substances 0.000 title claims description 23
- 238000005255 carburizing Methods 0.000 claims description 23
- 239000002344 surface layer Substances 0.000 claims description 15
- 229910000760 Hardened steel Inorganic materials 0.000 claims description 12
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 claims description 11
- 229910052799 carbon Inorganic materials 0.000 claims description 11
- 239000000203 mixture Substances 0.000 claims description 10
- 239000002245 particle Substances 0.000 claims description 8
- 239000012535 impurity Substances 0.000 claims description 5
- 229910000831 Steel Inorganic materials 0.000 description 30
- 239000010959 steel Substances 0.000 description 30
- 239000010410 layer Substances 0.000 description 18
- 150000001247 metal acetylides Chemical class 0.000 description 16
- 238000012360 testing method Methods 0.000 description 14
- 229910001566 austenite Inorganic materials 0.000 description 9
- 230000000694 effects Effects 0.000 description 8
- 238000005452 bending Methods 0.000 description 7
- 238000010791 quenching Methods 0.000 description 7
- 230000015572 biosynthetic process Effects 0.000 description 6
- 230000007423 decrease Effects 0.000 description 6
- 230000000171 quenching effect Effects 0.000 description 6
- 238000010438 heat treatment Methods 0.000 description 5
- 238000005496 tempering Methods 0.000 description 5
- 230000000717 retained effect Effects 0.000 description 4
- 229910052719 titanium Inorganic materials 0.000 description 4
- 229910000734 martensite Inorganic materials 0.000 description 3
- 238000001556 precipitation Methods 0.000 description 3
- 238000005728 strengthening Methods 0.000 description 3
- UCKMPCXJQFINFW-UHFFFAOYSA-N Sulphide Chemical compound [S-2] UCKMPCXJQFINFW-UHFFFAOYSA-N 0.000 description 2
- ATJFFYVFTNAWJD-UHFFFAOYSA-N Tin Chemical compound [Sn] ATJFFYVFTNAWJD-UHFFFAOYSA-N 0.000 description 2
- 230000002411 adverse Effects 0.000 description 2
- 229910045601 alloy Inorganic materials 0.000 description 2
- 239000000956 alloy Substances 0.000 description 2
- 230000006835 compression Effects 0.000 description 2
- 238000007906 compression Methods 0.000 description 2
- 238000005520 cutting process Methods 0.000 description 2
- 230000006866 deterioration Effects 0.000 description 2
- 238000010191 image analysis Methods 0.000 description 2
- 238000000034 method Methods 0.000 description 2
- 229910052750 molybdenum Inorganic materials 0.000 description 2
- 229910052759 nickel Inorganic materials 0.000 description 2
- 229910052758 niobium Inorganic materials 0.000 description 2
- 230000003647 oxidation Effects 0.000 description 2
- 238000007254 oxidation reaction Methods 0.000 description 2
- 238000012545 processing Methods 0.000 description 2
- 239000006104 solid solution Substances 0.000 description 2
- 229910052720 vanadium Inorganic materials 0.000 description 2
- 238000004458 analytical method Methods 0.000 description 1
- 230000033228 biological regulation Effects 0.000 description 1
- 229910001567 cementite Inorganic materials 0.000 description 1
- 238000010276 construction Methods 0.000 description 1
- 238000004453 electron probe microanalysis Methods 0.000 description 1
- 238000005516 engineering process Methods 0.000 description 1
- 238000005530 etching Methods 0.000 description 1
- 238000011156 evaluation Methods 0.000 description 1
- 238000002474 experimental method Methods 0.000 description 1
- 238000009661 fatigue test Methods 0.000 description 1
- 238000005098 hot rolling Methods 0.000 description 1
- KSOKAHYVTMZFBJ-UHFFFAOYSA-N iron;methane Chemical compound C.[Fe].[Fe].[Fe] KSOKAHYVTMZFBJ-UHFFFAOYSA-N 0.000 description 1
- 239000007788 liquid Substances 0.000 description 1
- 229910052748 manganese Inorganic materials 0.000 description 1
- 238000004519 manufacturing process Methods 0.000 description 1
- 238000005259 measurement Methods 0.000 description 1
- 238000000691 measurement method Methods 0.000 description 1
- 230000008520 organization Effects 0.000 description 1
- OXNIZHLAWKMVMX-UHFFFAOYSA-N picric acid Chemical compound OC1=C([N+]([O-])=O)C=C([N+]([O-])=O)C=C1[N+]([O-])=O OXNIZHLAWKMVMX-UHFFFAOYSA-N 0.000 description 1
- 230000001376 precipitating effect Effects 0.000 description 1
- 230000002035 prolonged effect Effects 0.000 description 1
- 230000001737 promoting effect Effects 0.000 description 1
- 239000000243 solution Substances 0.000 description 1
- 230000001629 suppression Effects 0.000 description 1
- 229910000859 α-Fe Inorganic materials 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C22—METALLURGY; FERROUS OR NON-FERROUS ALLOYS; TREATMENT OF ALLOYS OR NON-FERROUS METALS
- C22C—ALLOYS
- C22C38/00—Ferrous alloys, e.g. steel alloys
- C22C38/02—Ferrous alloys, e.g. steel alloys containing silicon
-
- C—CHEMISTRY; METALLURGY
- C21—METALLURGY OF IRON
- C21D—MODIFYING THE PHYSICAL STRUCTURE OF FERROUS METALS; GENERAL DEVICES FOR HEAT TREATMENT OF FERROUS OR NON-FERROUS METALS OR ALLOYS; MAKING METAL MALLEABLE, e.g. BY DECARBURISATION OR TEMPERING
- C21D1/00—General methods or devices for heat treatment, e.g. annealing, hardening, quenching or tempering
- C21D1/06—Surface hardening
-
- C—CHEMISTRY; METALLURGY
- C21—METALLURGY OF IRON
- C21D—MODIFYING THE PHYSICAL STRUCTURE OF FERROUS METALS; GENERAL DEVICES FOR HEAT TREATMENT OF FERROUS OR NON-FERROUS METALS OR ALLOYS; MAKING METAL MALLEABLE, e.g. BY DECARBURISATION OR TEMPERING
- C21D6/00—Heat treatment of ferrous alloys
- C21D6/002—Heat treatment of ferrous alloys containing Cr
-
- C—CHEMISTRY; METALLURGY
- C22—METALLURGY; FERROUS OR NON-FERROUS ALLOYS; TREATMENT OF ALLOYS OR NON-FERROUS METALS
- C22C—ALLOYS
- C22C38/00—Ferrous alloys, e.g. steel alloys
- C22C38/002—Ferrous alloys, e.g. steel alloys containing In, Mg, or other elements not provided for in one single group C22C38/001 - C22C38/60
-
- C—CHEMISTRY; METALLURGY
- C22—METALLURGY; FERROUS OR NON-FERROUS ALLOYS; TREATMENT OF ALLOYS OR NON-FERROUS METALS
- C22C—ALLOYS
- C22C38/00—Ferrous alloys, e.g. steel alloys
- C22C38/04—Ferrous alloys, e.g. steel alloys containing manganese
-
- C—CHEMISTRY; METALLURGY
- C22—METALLURGY; FERROUS OR NON-FERROUS ALLOYS; TREATMENT OF ALLOYS OR NON-FERROUS METALS
- C22C—ALLOYS
- C22C38/00—Ferrous alloys, e.g. steel alloys
- C22C38/18—Ferrous alloys, e.g. steel alloys containing chromium
- C22C38/26—Ferrous alloys, e.g. steel alloys containing chromium with niobium or tantalum
-
- C—CHEMISTRY; METALLURGY
- C22—METALLURGY; FERROUS OR NON-FERROUS ALLOYS; TREATMENT OF ALLOYS OR NON-FERROUS METALS
- C22C—ALLOYS
- C22C38/00—Ferrous alloys, e.g. steel alloys
- C22C38/18—Ferrous alloys, e.g. steel alloys containing chromium
- C22C38/28—Ferrous alloys, e.g. steel alloys containing chromium with titanium or zirconium
-
- C—CHEMISTRY; METALLURGY
- C23—COATING METALLIC MATERIAL; COATING MATERIAL WITH METALLIC MATERIAL; CHEMICAL SURFACE TREATMENT; DIFFUSION TREATMENT OF METALLIC MATERIAL; COATING BY VACUUM EVAPORATION, BY SPUTTERING, BY ION IMPLANTATION OR BY CHEMICAL VAPOUR DEPOSITION, IN GENERAL; INHIBITING CORROSION OF METALLIC MATERIAL OR INCRUSTATION IN GENERAL
- C23C—COATING METALLIC MATERIAL; COATING MATERIAL WITH METALLIC MATERIAL; SURFACE TREATMENT OF METALLIC MATERIAL BY DIFFUSION INTO THE SURFACE, BY CHEMICAL CONVERSION OR SUBSTITUTION; COATING BY VACUUM EVAPORATION, BY SPUTTERING, BY ION IMPLANTATION OR BY CHEMICAL VAPOUR DEPOSITION, IN GENERAL
- C23C8/00—Solid state diffusion of only non-metal elements into metallic material surfaces; Chemical surface treatment of metallic material by reaction of the surface with a reactive gas, leaving reaction products of surface material in the coating, e.g. conversion coatings, passivation of metals
- C23C8/06—Solid state diffusion of only non-metal elements into metallic material surfaces; Chemical surface treatment of metallic material by reaction of the surface with a reactive gas, leaving reaction products of surface material in the coating, e.g. conversion coatings, passivation of metals using gases
- C23C8/08—Solid state diffusion of only non-metal elements into metallic material surfaces; Chemical surface treatment of metallic material by reaction of the surface with a reactive gas, leaving reaction products of surface material in the coating, e.g. conversion coatings, passivation of metals using gases only one element being applied
- C23C8/20—Carburising
- C23C8/22—Carburising of ferrous surfaces
-
- C—CHEMISTRY; METALLURGY
- C23—COATING METALLIC MATERIAL; COATING MATERIAL WITH METALLIC MATERIAL; CHEMICAL SURFACE TREATMENT; DIFFUSION TREATMENT OF METALLIC MATERIAL; COATING BY VACUUM EVAPORATION, BY SPUTTERING, BY ION IMPLANTATION OR BY CHEMICAL VAPOUR DEPOSITION, IN GENERAL; INHIBITING CORROSION OF METALLIC MATERIAL OR INCRUSTATION IN GENERAL
- C23C—COATING METALLIC MATERIAL; COATING MATERIAL WITH METALLIC MATERIAL; SURFACE TREATMENT OF METALLIC MATERIAL BY DIFFUSION INTO THE SURFACE, BY CHEMICAL CONVERSION OR SUBSTITUTION; COATING BY VACUUM EVAPORATION, BY SPUTTERING, BY ION IMPLANTATION OR BY CHEMICAL VAPOUR DEPOSITION, IN GENERAL
- C23C8/00—Solid state diffusion of only non-metal elements into metallic material surfaces; Chemical surface treatment of metallic material by reaction of the surface with a reactive gas, leaving reaction products of surface material in the coating, e.g. conversion coatings, passivation of metals
- C23C8/80—After-treatment
-
- C—CHEMISTRY; METALLURGY
- C21—METALLURGY OF IRON
- C21D—MODIFYING THE PHYSICAL STRUCTURE OF FERROUS METALS; GENERAL DEVICES FOR HEAT TREATMENT OF FERROUS OR NON-FERROUS METALS OR ALLOYS; MAKING METAL MALLEABLE, e.g. BY DECARBURISATION OR TEMPERING
- C21D1/00—General methods or devices for heat treatment, e.g. annealing, hardening, quenching or tempering
- C21D1/18—Hardening; Quenching with or without subsequent tempering
- C21D1/25—Hardening, combined with annealing between 300 degrees Celsius and 600 degrees Celsius, i.e. heat refining ("Vergüten")
-
- C—CHEMISTRY; METALLURGY
- C21—METALLURGY OF IRON
- C21D—MODIFYING THE PHYSICAL STRUCTURE OF FERROUS METALS; GENERAL DEVICES FOR HEAT TREATMENT OF FERROUS OR NON-FERROUS METALS OR ALLOYS; MAKING METAL MALLEABLE, e.g. BY DECARBURISATION OR TEMPERING
- C21D2211/00—Microstructure comprising significant phases
- C21D2211/004—Dispersions; Precipitations
-
- C—CHEMISTRY; METALLURGY
- C21—METALLURGY OF IRON
- C21D—MODIFYING THE PHYSICAL STRUCTURE OF FERROUS METALS; GENERAL DEVICES FOR HEAT TREATMENT OF FERROUS OR NON-FERROUS METALS OR ALLOYS; MAKING METAL MALLEABLE, e.g. BY DECARBURISATION OR TEMPERING
- C21D2211/00—Microstructure comprising significant phases
- C21D2211/008—Martensite
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- Mechanical Engineering (AREA)
- Metallurgy (AREA)
- Organic Chemistry (AREA)
- Physics & Mathematics (AREA)
- Thermal Sciences (AREA)
- Crystallography & Structural Chemistry (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Heat Treatment Of Articles (AREA)
- Solid-Phase Diffusion Into Metallic Material Surfaces (AREA)
Description
本発明は、建産機や自動車の分野で用いられる機械構造用材料に供する、冷間鍛造性に優れかつ浸炭により高い疲労強度を有する肌焼鋼および高疲労強度浸炭材に関するものである。 The present invention relates to a case-hardening steel and a high fatigue strength carburized material that are excellent in cold forgeability and have high fatigue strength by carburization, which are used for machine structural materials used in the fields of construction machinery and automobiles.
棒鋼を冷間成形して製造される、例えば自動車等の部品素材には、高い冷間鍛造性が要求される。そのため、球状化熱処理を施して炭化物を球状化し、冷間鍛造性を高めることが行われている。また、鋼の成分組成の観点からは、変形抵抗に大きく影響するSiを低減するなどの提案もなされている。更に、Bの焼入れ性を有効活用した鋼の提案もある。 High cold forgeability is required for parts materials such as automobiles manufactured by cold forming steel bars. Therefore, spheroidizing heat treatment is performed to spheroidize carbides to improve cold forgeability. In addition, from the viewpoint of the composition of steel, proposals have been made to reduce Si, which greatly affects deformation resistance. Furthermore, there is a proposal of steel that effectively uses the hardenability of B.
例えば、特許文献1には、Bの焼入れ性向上の効果分だけ他の合金元素を減量することによって、焼ならし工程から硬さを低くし、従来鋼に対して歯切り性を飛躍的に向上させた、浸炭歯車用鋼が提案されている。 For example, in Patent Document 1, by reducing the amount of other alloy elements by the effect of improving the hardenability of B, the hardness is reduced from the normalizing step, and the cutting performance is dramatically improved compared to conventional steel. Improved carburized gear steels have been proposed.
また、特許文献2では、固溶強化元素であるSiおよびMnを低減して焼入れ性をBで確保する成分系と、製造条件との組み合わせにより、冷間加工性を確保する肌焼鋼が提案されている。 Patent Document 2 proposes a case-hardening steel that secures cold workability by combining the component system that secures hardenability with B by reducing the solid solution strengthening elements Si and Mn and the manufacturing conditions. Has been.
一方で、近年、自動車等に用いられる歯車等には、省エネルギー化による車体重量の軽量化に伴って、サイズの小型化が要求され、またエンジンの高出力化に伴って歯車にかかる負荷も増大している。歯車の耐久性は、主に歯元曲げ疲労破壊ならびに歯面の面圧疲労破壊によってきまる。歯元曲げ疲労強度については、浸炭時に表層に生じる不完全焼き入れ層の低減や、旧オーステナイト粒径の微細化が有効であるとされている。また、面圧疲労強度の向上については、焼戻し軟化抵抗性との関連が指摘され、Si量を高めた成分や、Moを添加した成分、または浸炭表層に微細な炭化物を分散させた鋼が、それぞれ提案されている。 On the other hand, in recent years, gears used in automobiles and the like have been required to be smaller in size as the weight of the vehicle body has been reduced due to energy saving, and the load on the gears has increased as the output of the engine has increased. doing. The durability of gears is determined mainly by the root bending fatigue failure and the surface pressure fatigue failure of the tooth surface. Regarding the root bending fatigue strength, it is considered effective to reduce the incompletely hardened layer generated in the surface layer during carburizing and to refine the prior austenite grain size. In addition, regarding the improvement of surface fatigue strength, the relationship with temper softening resistance has been pointed out, and components with increased Si content, components with Mo added, or steel with fine carbides dispersed in the carburized surface layer, Each has been proposed.
例えば、特許文献3には、旧オーステナイト粒径を7μm以下にすることによって、疲労強度と靭性を改善した浸炭用鋼が提案されている。また、特許文献4には、表面の浸炭層に炭化物を微細分散させることが提案されている。 For example, Patent Document 3 proposes a steel for carburizing in which fatigue strength and toughness are improved by setting the prior austenite grain size to 7 μm or less. Patent Document 4 proposes finely dispersing carbide in a carburized layer on the surface.
しかしながら、上述した特許文献1および2では、冷間加工性や衝撃特性の向上は認められるが、疲労特性は従来鋼と同等程度である。
また、特許文献3および4では、Nb、TiおよびVなどの炭化物生成元素を多量に使用し、微細析出した場合に加工時の変形抵抗を著しく上昇させる等の問題があった。
However, in Patent Documents 1 and 2 described above, improvements in cold workability and impact properties are recognized, but fatigue properties are comparable to conventional steel.
Further, Patent Documents 3 and 4 have a problem that, when a large amount of carbide generating elements such as Nb, Ti, and V are used and finely precipitated, deformation resistance during processing is remarkably increased.
本発明は、上記の実情に鑑み開発されたものであり、その目的とするところは、冷間鍛造性に優れるだけでなく浸炭処理後に高い耐疲労強度を有する肌焼鋼およびこれを用いた浸炭材を提供することにある。 The present invention has been developed in view of the above circumstances, and the object thereof is not only excellent in cold forgeability but also case hardening steel having high fatigue resistance after carburizing treatment and carburizing using the same. To provide materials.
発明者らは、上記の課題を解決すべく鋭意研究を重ねた結果、以下に述べる知見を得た。まず、耐疲労強度を向上するために、肌焼鋼にC濃度0.85質量%以上の高C濃度浸炭層(以下、高濃度浸炭層という)を形成させた場合に、浸炭表層において、粗大な炭化物(主にセメンタイト)の生成を抑制して炭化物を微細に分散させるための方途を鋭意究明した。
すなわち、図1に、肌焼鋼の高濃度浸炭層の表層における、炭化物の最大粒子径に及ぼすAl、BおよびTi量の関係を示す。同図からわかるように、粗大な炭化物の生成を抑制し、炭化物を微細に分散させるためには、AlおよびB量の制御とTi添加量の抑制とが重要である。ここで、図1には、一部の鋼に関して面疲労強度を測定した結果についても示したが、粗大な炭化物の生成の抑制により、高い面疲労強度が得られることもわかる。
また、肌焼鋼にC濃度0.70〜0.84質量%の浸炭層(以下、通常浸炭層という)を形成させた場合について、面疲労強度に及ぼすAl、TiおよびB量の関係についても調査した。その結果を図1に併せて示す。通常浸炭層を形成させた場合においても、AlおよびB量を特定範囲に制御し、かつ、Tiを0.003質量%以下に抑制すると高い面疲労強度が得られることがわかる。
As a result of intensive studies to solve the above problems, the inventors have obtained the following knowledge. First, in order to improve the fatigue strength, when a high C concentration carburized layer (hereinafter referred to as a high concentration carburized layer) having a C concentration of 0.85% by mass or more is formed on the case-hardened steel, We have intensively studied ways to finely disperse carbides by suppressing the formation of (mainly cementite).
That is, FIG. 1 shows the relationship among the amounts of Al, B, and Ti on the maximum particle diameter of carbides in the surface layer of the high-concentration carburized layer of case hardening steel. As can be seen from the figure, in order to suppress the formation of coarse carbides and finely disperse the carbides, it is important to control the amounts of Al and B and to suppress the amount of Ti added. Here, FIG. 1 also shows the results of measuring the surface fatigue strength of some steels, but it can also be seen that high surface fatigue strength can be obtained by suppressing the formation of coarse carbides.
In addition, when a carburized layer having a C concentration of 0.70 to 0.84% by mass (hereinafter referred to as a normal carburized layer) was formed on the case-hardened steel, the relationship among the amounts of Al, Ti, and B on the surface fatigue strength was also investigated. The results are also shown in FIG. Even when a normal carburized layer is formed, it can be seen that high surface fatigue strength can be obtained by controlling the amounts of Al and B within a specific range and suppressing Ti to 0.003 mass% or less.
なお、図1に結果を示す実験は、0.2質量%C−0.1質量%Si-0.6質量%Mn−1.5質量%Cr−0.02質量%Nb鋼を基本として、この基本組成に種々の含有量のAlおよびBを添加した鋼素材を準備し(残部はFeおよび不可避的不純物)、これら鋼素材に以下の条件の処理を施した後の、炭化物の最大粒子径(μm)および面疲労強度(MPa)を評価したものである。
すなわち、高濃度浸炭については、鋼素材より、25mmφ丸棒を加工し、カーボンポテンシャル2%、950℃で5時間の高濃度浸炭を行い、一旦600℃に冷却した後、再度850℃で30分保持し、60℃で油冷後、170℃で2時間の焼戻し処理を行った。この処理を行ったサンプルを切断した後、切断面をピラクール液で腐食し、表面から30μm深さまでの領域を走査型電子顕微鏡で6000μm2にわたって観察し、画像解析により炭化物の最大粒子径を求めた。また、上記丸棒よりローラピッチング試験片を採取し、これに上述の高濃度浸炭から焼戻し処理までの各処理を施したサンプルに対し、すべり率40%および油温80℃の条件でローラピッチング試験を行い、107回強度(試験片表面にピッチングが発生する限界強度)を評価した。
また、通常浸炭については、鋼素材より、25mmφ丸棒を加工し、この丸棒よりローラピッチング試験片を採取し、これに930℃、7時間、カーボンポテンシャル1.1質量%の条件で浸炭を実施後、60℃で油冷し、170℃、2時間の焼戻し処理を施した。このようにして得られたサンプルに対し、すべり率40%および油温80℃の条件でローラピッチング試験を行い、107回強度(試験片表面にピッチングが発生する限界強度)を評価した。
The experiment whose results are shown in FIG. 1 is based on 0.2 mass% C-0.1 mass% Si-0.6 mass% Mn-1.5 mass% Cr-0.02 mass% Nb steel. And B added steel materials (the balance is Fe and inevitable impurities), and after these steel materials are treated under the following conditions, the maximum particle size (μm) and surface fatigue strength (MPa) of carbides Is evaluated.
That is, for high-concentration carburization, a 25mmφ round bar is processed from steel material, carbon concentration is 2%, high-concentration carburization at 950 ℃ for 5 hours, once cooled to 600 ℃, then again at 850 ℃ for 30 minutes It was kept, oil cooled at 60 ° C., and then tempered at 170 ° C. for 2 hours. After cutting the sample subjected to this treatment, the cut surface was corroded with Piracool liquid, the region from the surface to a depth of 30 μm was observed over a scanning electron microscope over 6000 μm 2, and the maximum particle size of the carbide was determined by image analysis. . In addition, a roller pitching test piece was collected from the round bar, and a roller pitching test was performed on the samples subjected to the above-described high-concentration carburization to tempering treatment at a sliding rate of 40% and an oil temperature of 80 ° C. And the strength was evaluated 10 7 times (the limit strength at which pitting occurs on the surface of the test piece).
For normal carburizing, a 25mmφ round bar is machined from a steel material, and a roller pitching test piece is taken from this round bar, and then carburized under conditions of 930 ° C, 7 hours, and carbon potential of 1.1% by mass. Then, it was oil-cooled at 60 ° C. and tempered at 170 ° C. for 2 hours. Thus to the sample thus obtained is subjected to roller pitting test under the conditions of the slip ratio of 40% and oil temperature 80 ° C., was evaluated (pitching limiting intensity generated in the test piece surface) 10 7 times the strength.
すなわち、本発明の要旨構成は、以下のとおりである。
(1)C:0.10〜0.35質量%、
Si:0.01〜0.50質量%、
Mn:0.40〜1.50質量%、
P:0.02質量%以下、
S:0.03質量%以下、
Al:0.04〜0.10質量%、
Cr:0.5〜2.5質量%、
B:0.0005〜0.0050質量%、
Nb:0.003〜0.080質量%、
Ti:0.003質量%以下および
N:0.0080質量%未満
を含有し、残部はFe及び不可避不純物からなる成分組成を有する肌焼鋼に対して浸炭が施されてなる、浸炭材であって、表面から0.4mmまでの表層域における炭素量が0.85質量%以上であり、該表層域における、炭化物の最大径が10μm以下、かつ平均粒子径が4μm以下である浸炭材。
That is, the gist configuration of the present invention is as follows.
(1) C: 0.10 to 0.35 mass%,
Si: 0.01 to 0.50 mass%,
Mn: 0.40-1.50 mass%,
P: 0.02 mass% or less,
S: 0.03 mass% or less,
Al: 0.04 to 0.10% by mass,
Cr: 0.5 to 2.5% by mass,
B: 0.0005-0.0050 mass%,
Nb: 0.003 to 0.080 mass%,
Ti: 0.003 mass% or less and N: less than 0.0080 mass%, and the balance is carburized material obtained by carburizing case- hardened steel having a component composition composed of Fe and inevitable impurities, from the surface A carburized material having a carbon content in a surface layer region of up to 0.4 mm of 0.85% by mass or more, a maximum carbide diameter of 10 μm or less, and an average particle size of 4 μm or less in the surface layer region .
(2)前記成分組成は、更に、
Cu:1.0質量%以下、
Ni:0.50質量%以下、
Mo:0.50質量%以下および
V:0.5質量%以下
のうちから選ばれる1種または2種以上を含有する前記(1)に記載の浸炭材。
(2) The component composition further includes:
Cu: 1.0 mass% or less,
Ni: 0.50 mass% or less,
The carburizing material according to (1), containing one or more selected from Mo: 0.50% by mass or less and V: 0.5% by mass or less.
(3)前記成分組成は、更に、
Ca:0.0005〜0.0050質量%および
Mg:0.0002〜0.0020質量%
の1種または2種を含有する前記(1)または(2)に記載の浸炭材。
(3) The component composition further includes:
Ca: 0.0005 to 0.0050 mass% and
Mg: 0.0002 to 0.0020 mass%
The carburizing material according to (1) or (2), which contains one or two of the above .
本発明によれば、冷間鍛造性に優れるだけでなく、浸炭処理後の耐疲労強度にも優れた肌焼鋼を提供でき、工業上非常に有用である。 According to the present invention, it is possible to provide a case-hardened steel that is not only excellent in cold forgeability but also excellent in fatigue resistance after carburizing treatment, which is very useful industrially.
以下、本発明の肌焼鋼を具体的に説明する。
まず、本発明において、鋼の成分組成を上記の範囲に限定した理由について、成分毎に詳しく説明する。
C:0.10〜0.35質量%
浸炭熱処理後の焼入れにより中心部の硬度を高めるために、0.10質量%以上のCを必要とするが、含有量が0.35質量%を増えると、芯部の靭性が低下するため、C量は0.10〜0.35質量%の範囲に限定した。好ましくは、0.3質量%以下の範囲である。
Hereinafter, the case-hardened steel of the present invention will be specifically described.
First, the reason why the component composition of steel is limited to the above range in the present invention will be described in detail for each component.
C: 0.10 to 0.35 mass%
In order to increase the hardness of the central part by quenching after the carburizing heat treatment, 0.10% by mass or more of C is required, but when the content increases by 0.35% by mass, the toughness of the core part decreases, so the C amount is 0.10%. It was limited to the range of ˜0.35 mass%. Preferably, it is 0.3 mass% or less.
Si:0.01〜0.50質量%
Siは、脱酸剤として必要であり、少なくとも0.01質量%以上の添加が必要である。しかしながら、Siは浸炭表層で優先的に酸化し、粒界酸化を促進する元素である。また、フェライトを固溶強化し変形抵抗を高めて冷間鍛造性を劣化させるため、上限を0.50質量%とする。好ましくは0.03〜0.35質量%である。
Si: 0.01 to 0.50 mass%
Si is necessary as a deoxidizing agent, and at least 0.01% by mass or more must be added. However, Si is an element that preferentially oxidizes in the carburized surface layer and promotes grain boundary oxidation. In addition, the upper limit is set to 0.50% by mass in order to enhance the solid solution strengthening of ferrite and increase the deformation resistance to deteriorate the cold forgeability. Preferably it is 0.03-0.35 mass%.
Mn:0.40〜1.50質量%
Mnは、焼入性の向上に有効な元素で有り、少なくとも0.40質量%の添加を必要とする。しかし、Mnは粒界酸化を引き起こしやすく、また過剰な添加は残留オーステナイトを増加させ、表面硬さの低下を招くことから、上限を1.50質量%とした。好ましくは0.60〜1.40質量%の範囲である。
Mn: 0.40 to 1.50 mass%
Mn is an element effective for improving the hardenability, and requires addition of at least 0.40% by mass. However, Mn tends to cause grain boundary oxidation, and excessive addition increases residual austenite, leading to a decrease in surface hardness, so the upper limit was made 1.50% by mass. Preferably it is the range of 0.60-1.40 mass%.
P:0.02質量%以下
Pは、結晶粒界に偏析し、靭性を低下させるため、その混入は低いほど望ましいが、0.02質量%までは許容される。好ましくは、0.018質量%以下である。
P: 0.02% by mass or less P is segregated at the grain boundary and lowers the toughness. Therefore, the lower the content, the better, but 0.02% by mass is acceptable. Preferably, it is 0.018 mass% or less.
S:0.03質量%以下
Sは、硫化物系介在物として存在し、被削性の向上に有効な元素である。しかしながら、過剰な添加は疲労強度の低下を招くため、上限を0.03質量%とした。
S: 0.03 mass% or less S is an element that exists as sulfide inclusions and is effective in improving machinability. However, excessive addition causes a decrease in fatigue strength, so the upper limit was made 0.03% by mass.
Al:0.04〜0.10質量%
Alは、鋼中のNをAlNとして固定することによって、Bの焼入れ性効果を得るための重要な元素である。この効果を得るためには、少なくとも0.04質量%の添加が必要である。しかしながら、含有量が0.10質量%を超えると、疲労強度に対して有害なA1203介在物の生成を助長するため、Al量は0.04〜0.10質量%の範囲に限定した。
Al: 0.04-0.10 mass%
Al is an important element for obtaining the hardenability effect of B by fixing N in steel as AlN. In order to obtain this effect, it is necessary to add at least 0.04% by mass. However, if the content exceeds 0.10 mass%, in order to facilitate the generation of harmful A1 2 0 3 inclusions against fatigue strength, Al content is limited to the range of 0.04 to 0.10 wt%.
Cr:0.5〜2.5質量%
Crは、焼入性のみならず、焼戻し軟化抵抗の向上に寄与し、さらには炭化物の球状化促進にも有用な元素であるが、含有量が0.5質量%に満たないと、その添加効果に乏しく、一方、2.5質量%を超えると、浸炭部での残留オーステナイトの生成を促進し、疲労強度に悪影響を与える場合がある。よって、Cr量は0.5〜2.5質量%の範囲に限定した。好ましくは0.6〜2.0質量%の範囲である。
Cr: 0.5-2.5% by mass
Cr is an element that contributes not only to hardenability but also to improving resistance to temper softening, and also useful for promoting the spheroidization of carbides. On the other hand, if it exceeds 2.5% by mass, the formation of retained austenite in the carburized part is promoted, and the fatigue strength may be adversely affected. Therefore, the Cr content is limited to the range of 0.5 to 2.5 mass%. Preferably it is the range of 0.6-2.0 mass%.
B:0.0005〜0.0050質量%
Bは、本発明において最も重要な元素である。Bは、焼入れ熱処理時にオーステナイト粒界に偏析することで焼入れ性を高め、素材の硬度上昇に寄与する。この効果により、他の強化元素を削減でき、その結果、変形抵抗の低下による冷間鍛造性の向上が得られる。この効果を発揮するためには、少なくとも0.0005質量%以上の添加が必要である。一方、過剰な添加は、靭性や鍛造性などの低下を招くことから、上限を0.0050質量%とした。好ましいB含有量の上限は、0.0030質量%である。
B: 0.0005 to 0.0050 mass%
B is the most important element in the present invention. B segregates at the austenite grain boundaries during the quenching heat treatment, thereby improving the hardenability and contributing to an increase in the hardness of the material. By this effect, other strengthening elements can be reduced, and as a result, an improvement in cold forgeability due to a decrease in deformation resistance can be obtained. In order to exhibit this effect, it is necessary to add at least 0.0005% by mass or more. On the other hand, excessive addition causes a decrease in toughness, forgeability, etc., so the upper limit was made 0.0050% by mass. A preferable upper limit of the B content is 0.0030% by mass.
Nb:0.003〜0.080質量%
Nbは、鋼中でNbCを形成し、浸炭熱処理時のオーステナイト粒径の粗粒化をピン止め効果により抑制する。この効果を得るためには、少なくとも0.003質量%以上の添加が必要である。一方、0.080質量%を超えて添加すると、粗大なNbCの析出による粗粒化抑制能の低下や疲労強度の劣化を招く、おそれがあるため、0.080質量%以下とする。好ましくは、0.010〜0.060質量%である。
Nb: 0.003 to 0.080 mass%
Nb forms NbC in the steel and suppresses the coarsening of the austenite grain size during the carburizing heat treatment by the pinning effect. In order to obtain this effect, at least 0.003% by mass or more must be added. On the other hand, if added over 0.080% by mass, there is a risk of reducing the coarsening suppression ability and deterioration of fatigue strength due to coarse precipitation of NbC, so 0.080% by mass or less. Preferably, it is 0.010-0.060 mass%.
Ti:0.003質量%以下
Tiは、鋼中への混入を極力回避することが好ましい成分である。Tiは、Nと結合し、粗大なTiNを形成しやすい。かように、浸炭表層の炭化物の粗大化や疲労強度の低下を招くため、上限を0.003質量%とする。
Ti: 0.003 mass% or less
Ti is a component that preferably avoids mixing into steel as much as possible. Ti bonds with N and easily forms coarse TiN. In this way, the upper limit is set to 0.003 mass% in order to cause coarsening of the carbide on the carburized surface layer and decrease in fatigue strength.
N:0.008質量%未満
Nは、鋼中への混入を極力回避することが好ましい成分である。従って、Nは、Bの焼入れ性を確保することと、TiNの形成を抑制するために、0.008質量%未満とした。
N: Less than 0.008% by mass N is a component that preferably avoids mixing into steel as much as possible. Therefore, N is made less than 0.008% by mass in order to secure the hardenability of B and to suppress the formation of TiN.
また、本発明では、焼入性を高めるために上記成分に、更に、Cu:1.0質量%以下、Ni:0.50質量%以下、Mo:0.5質量%以下およびV:0.5質量%以下のうちから選ばれる1種または2種以上を含有することができる。
Cuは、焼き入れ性の向上に有効な元素であり、好ましくは0.1質量%以上で添加するが、多量の添加は鋼材の表面性状の劣化や合金コストの増加を招くため、上限を1.0質量%とした。
In the present invention, in order to improve hardenability, the above components are further selected from Cu: 1.0 mass% or less, Ni: 0.50 mass% or less, Mo: 0.5 mass% or less, and V: 0.5 mass% or less. 1 type, or 2 or more types can be contained.
Cu is an element effective for improving hardenability, and is preferably added in an amount of 0.1% by mass or more. However, addition of a large amount leads to deterioration of the surface properties of steel materials and an increase in alloy costs, so the upper limit is 1.0% by mass. It was.
Ni、MoおよびVは、焼入れ性や靭性の向上に有効な元素であり、好ましくはそれぞれ0.1質量%以上、0.05質量%以上および0.02質量%以上であるが、高価であることから上限をそれぞれ0.50質量%とした。 Ni, Mo, and V are effective elements for improving hardenability and toughness, and are preferably 0.1% by mass or more, 0.05% by mass or more, and 0.02% by mass or more, respectively. It was set as mass%.
また、本発明では、硫化物の形態を制御し、被削性や冷間鍛造性を高めるために、上記成分に更に、Ca:0.0005〜0.0050質量%およびMg:0.0002〜0.0020質量%の1種または2種を含有することが出来る。
すなわち、CaおよびMgによる上記効果を得るには、各々、少なくとも0.0005質量%、0.0002質量%の添加が必要である。一方、過剰に添加した場合には、粗大な介在物を形成し、疲労強度に悪影響を与えるため、CaおよびMgについて上限をそれぞれ0.0050質量%および0.0020質量%とした。
以上説明した元素以外の残部は、Feおよび不可避的不純物である。
Further, in the present invention, in order to control the form of the sulfide and improve the machinability and cold forgeability, the above components are further added to one of Ca: 0.0005 to 0.0050 mass% and Mg: 0.0002 to 0.0020 mass%. Or it can contain 2 types.
That is, in order to obtain the above effects by Ca and Mg, it is necessary to add at least 0.0005 mass% and 0.0002 mass%, respectively. On the other hand, when excessively added, coarse inclusions are formed and the fatigue strength is adversely affected. Therefore, the upper limits of Ca and Mg were set to 0.0050 mass% and 0.0020 mass%, respectively.
The balance other than the elements described above is Fe and inevitable impurities.
以上説明した成分組成の肌焼鋼に対して、冷間加工を施して部品形状とした後、浸炭処理を施す。浸炭処理は、肌焼鋼に一般に行なわれている条件(以下通常浸炭と言う)にて実施することができる。すなわち、カーボンポテンシャル0.8〜1.1質量%、900℃以上で3〜7時間保持することで、少なくとも表層0.4mmまでのC濃度が0.7質量%以上となる浸炭層を表層に形成させる。浸炭層を形成させた後には、通常肌焼鋼に対して施される焼入れ・焼戻しを施す。すなわち、60〜140℃の油で焼入れを行い表層(浸炭層)の組織を残留オーステナイト10〜40%を含むマルテンサイト組織とし、その後160〜200℃で1〜2時間の焼戻しを施すことで、回転曲げ疲労強度および面疲労強度に優れた浸炭材を得ることができる。なお、浸炭層形成のための温度は、浸炭層形成を長時間化させないために900℃以上とすることが好ましく、浸炭炉の耐久性の観点からは950℃以下とすることが好ましい。また、焼入れ処理時の油の温度は、焼入れ時に材料の変形を抑制する観点から60℃以上とすることが好ましく、必要な鋼組織(残留オーステナイト10〜40%を含むマルテンサイト組織)を得て硬さを確保する観点からは140℃以下とすることが好ましい。通常浸炭における浸炭層のC濃度は0.85質量%未満である。
また、本発明の肌焼鋼材は、上記した通常浸炭に対して、浸炭層のC濃度を0.85質量%以上にまで高め、炭化物を析出させることで浸炭層の硬さをさらに高めて面疲労強度を向上させることを目的とした高濃度浸炭に特に適している。高濃度浸炭の場合、従来用いられている肌焼鋼では、粗大炭化物の量が多くなり、面疲労強度のさらなる向上は期待できない。しかし、本発明の肌焼鋼では、浸炭層のC濃度を0.85質量%以上にまで高めても粗大炭化物の析出を抑制でき、面疲労強度が向上する。すなわち、浸炭処理後は、表面下0.4mmまでの表層域において、炭素量は0.85質量%以上であり、ここに形成される炭化物の最大径は10μm以下かつ平均粒子径は4μm以下とすることができる。この範囲内であれば、特に面疲労強度の向上に効果がある。逆に、この範囲を超えると、さらなる面疲労強度の向上は期待できない。
The case-hardened steel having the component composition described above is subjected to a cold carving process and then carburized. The carburizing treatment can be performed under the conditions generally used for case-hardened steel (hereinafter referred to as normal carburizing). That is, by holding at a carbon potential of 0.8 to 1.1 mass% and 900 ° C. or more for 3 to 7 hours, a carburized layer having a C concentration of 0.7 mass% or more at least up to a surface layer of 0.4 mm is formed on the surface layer. After the carburized layer is formed, quenching and tempering that is usually applied to case-hardened steel is performed. That is, by quenching with oil at 60 to 140 ° C. and making the structure of the surface layer (carburized layer) into a martensite structure containing 10 to 40% of retained austenite, and then tempering at 160 to 200 ° C. for 1 to 2 hours, A carburized material excellent in rotational bending fatigue strength and surface fatigue strength can be obtained. The temperature for forming the carburized layer is preferably 900 ° C. or higher so that the carburized layer formation is not prolonged, and is preferably 950 ° C. or lower from the viewpoint of the durability of the carburizing furnace. Moreover, it is preferable that the temperature of the oil at the time of quenching is 60 ° C. or more from the viewpoint of suppressing deformation of the material at the time of quenching, and a necessary steel structure (a martensite structure including 10 to 40% of retained austenite) is obtained. From the viewpoint of ensuring hardness, the temperature is preferably 140 ° C. or lower. The C concentration in the carburized layer in normal carburizing is less than 0.85% by mass.
Further, the case-hardened steel material of the present invention increases the C concentration of the carburized layer to 0.85% by mass or more with respect to the normal carburizing described above, and further increases the hardness of the carburized layer by precipitating carbides, thereby increasing the surface fatigue strength. It is particularly suitable for high-concentration carburizing for the purpose of improving the quality. In the case of high-concentration carburizing, the amount of coarse carbide increases in conventionally used case-hardened steel, and further improvement in surface fatigue strength cannot be expected. However, in the case-hardened steel of the present invention, even if the C concentration of the carburized layer is increased to 0.85% by mass or more, precipitation of coarse carbides can be suppressed and surface fatigue strength is improved. That is, after the carburization treatment, the carbon content is 0.85 mass% or more in the surface layer region up to 0.4 mm below the surface, and the maximum diameter of the carbide formed here is 10 μm or less and the average particle diameter is 4 μm or less. it can. Within this range, the surface fatigue strength is particularly improved. Conversely, if this range is exceeded, further improvement in surface fatigue strength cannot be expected.
表層域の炭素量が0.85質量%未満では、十分な量の炭化物が得られず面疲労強度のさらなる向上が図れない。また、炭化物の最大径が10μm超になると、粗大な炭化物が疲労亀裂の起点になる等により、疲労寿命が低下する。平均粒子径が4μmを超える場合に
おいても同様に、疲労寿命の低下を招く。
If the amount of carbon in the surface layer area is less than 0.85% by mass, a sufficient amount of carbide cannot be obtained, and the surface fatigue strength cannot be further improved. In addition, when the maximum diameter of carbide exceeds 10 μm, the fatigue life is reduced due to the coarse carbide becoming the starting point of fatigue cracks. Similarly, when the average particle diameter exceeds 4 μm, the fatigue life is reduced.
なお、上記の規定に従う炭化物を得るには、浸炭熱処理を次の条件下に行うことが好ましい。すなわち、カーボンポテンシャル1.2〜2.5質量%、930〜1050℃で1〜5時間程度保持して浸炭を行ない、一旦550〜650℃に冷却して、その後に、再度830〜880℃で30〜60分保持した後、60〜140℃の油にて焼入れを施し、その後焼戻しを施すことが好ましく、焼戻し温度は170〜200℃の範囲が好ましい。以上の処理を行なうことで、表層に形成させた浸炭層の鋼組織は、上記のとおり炭化物が最大径10μm以下、平均粒子径4μm以下に微細に分散した、残留オーステナイトを10〜40%を含むマルテンサイト組織となる。 In addition, in order to obtain the carbide according to said prescription | regulation, it is preferable to perform carburizing heat processing on the following conditions. That is, the carbon potential is kept at 1.2 to 2.5 mass%, held at 930 to 1050 ° C for about 1 to 5 hours, carburized, once cooled to 550 to 650 ° C, and then again at 830 to 880 ° C for 30 to 60 minutes. After holding, it is preferable to quench with oil at 60 to 140 ° C. and then temper, and the tempering temperature is preferably within the range of 170 to 200 ° C. By performing the above treatment, the steel structure of the carburized layer formed on the surface layer contains 10-40% of retained austenite in which carbides are finely dispersed to a maximum diameter of 10 μm or less and an average particle diameter of 4 μm or less as described above. Become a martensite organization.
次に、本発明の実施例について説明する。
表1に示す成分組成の鋼(残部はFeおよび不可避的不純物)を溶製し、一旦1150℃以上に加熱した後、170mm×170mm角断面の中間素材とし、更にAc3+100℃以上に加熱した後、熱間圧延により直径60mmの丸棒に成形した。得られた棒鋼について、冷間鍛造性の評価を行った。
Next, examples of the present invention will be described.
Steel with the composition shown in Table 1 (the balance is Fe and inevitable impurities) was melted and heated to 1150 ° C or higher, then used as an intermediate material with a 170 mm x 170 mm square cross section, and further heated to Ac 3 + 100 ° C or higher. Thereafter, it was formed into a round bar having a diameter of 60 mm by hot rolling. The obtained bar steel was evaluated for cold forgeability.
ここで、冷間加工性は、限界据え込み率および変形抵抗の2項目で評価した。
すなわち、棒鋼の表面から直径の1/4の深さ位置(1/4D位置)から、直径:10mmおよび高さ:15mmの試験片を採取し、300tプレス機を用いて、60%据え込み時の圧縮荷重を
測定し、日本塑性加工学会が提唱している端面拘束圧縮により変形抵抗測定方法を用いて求めた。
また、限界据え込み率は、変形抵抗を測定した方法で圧縮加工を行い、端部に割れが入ったときの据え込み率を限界据え込み率とした。変形抵抗値が899MPa以下、限界割れ率が74%以上であれば、冷聞鍛造性は良好であるといえる。
Here, the cold workability was evaluated by two items, the limit upsetting rate and the deformation resistance.
In other words, a specimen with a diameter of 10 mm and a height of 15 mm was taken from a depth position (1 / 4D position) of 1/4 of the diameter from the surface of the steel bar, and installed at 60% using a 300-ton press. The compression load was measured, and the deformation resistance measurement method was obtained by end face constrained compression proposed by the Japan Society for Technology of Plasticity.
Further, the limit upsetting rate was defined as the upsetting rate when the end portion was cracked by compressing by a method of measuring deformation resistance. If the deformation resistance value is 899 MPa or less and the critical crack rate is 74% or more, it can be said that the cold forgeability is good.
次に、疲労特性は、回転曲げ疲労と面疲労の2項目で評価した。
すなわち、上記の棒鋼の1/4D位置から回転曲げ試験片とローラーピッチング試験片を採取し、これらの試験片に通常浸炭と炭化物を多く生成させるための高濃度浸炭との2種類の熱処理を行った。通常浸炭は930℃、7時間、カーボンポテンシャル1.1質量%の条件で浸炭を実施後、60℃で油冷し、170℃、2時間の焼戻し処理を施した。一方、高濃度浸
炭は、950℃、5時間、カーボンポテンシャル2質量%の条件で保持し、一旦600℃に冷却した後、再度850℃に30分保持し、60℃で油冷後、170℃、2時間の焼戻し処理を施した。
Next, the fatigue characteristics were evaluated by two items of rotational bending fatigue and surface fatigue.
That is, rotating bending test pieces and roller pitching test pieces are collected from 1 / 4D positions of the above steel bars, and two types of heat treatment are performed on these test pieces: normal carburizing and high-concentration carburizing to generate a large amount of carbides. It was. Normally, carburization was performed at 930 ° C for 7 hours under conditions of carbon potential of 1.1% by mass, and then oil-cooled at 60 ° C and tempered at 170 ° C for 2 hours. On the other hand, high-concentration carburization is held at 950 ° C for 5 hours under the condition of 2% by mass of carbon potential, once cooled to 600 ° C, then again held at 850 ° C for 30 minutes, oil-cooled at 60 ° C and 170 ° C A tempering treatment for 2 hours was performed.
ここで、浸炭後の炭化物の測定は、ピクラール液でエッチング後に、表面から30μm深さまでの領域を走査電子顕微鏡で6000μm2にわたって観察し、画像解析にて炭化物の最大径および平均径を求めた。すなわち、円相当径の最大値をもって最大径とし、また円相当径の平均値をもって平均径とした。なお、表面から0.4mmまでの他の深さ領域についても、炭化物の観察を行ったが、表面から30μm深さまでが最大径並びに平均径ともに最も大きいことを確認した。ここで、炭化物の観察では、円相当径が0.5μm以上のものが炭化物として識別可能である。
なお、炭素濃度の測定は、表面から深さ0.4mmまでをEPMAライン分析することにより
行った。
上記浸炭後の各試験片につき、回転曲げ試験およびローラーピッチング試験を行った。まず、回転曲げ疲労試験は、回転数3500rpmで実施し、107回の耐疲労強度にて評価した。また、ローラーピッチング試験は、すべり率40%、油温80℃の条件で107回強度(試験片表面にピッチングが発生する限界強度)で評価した。
得られた評価結果を表2に示す。
Here, in the measurement of the carbide after carburizing, after etching with a picral solution, a region from the surface to a depth of 30 μm was observed with a scanning electron microscope over 6000 μm 2 and the maximum diameter and average diameter of the carbide were obtained by image analysis. That is, the maximum value of the equivalent circle diameter was defined as the maximum diameter, and the average value of the equivalent circle diameter was defined as the average diameter. Carbides were also observed in other depth regions from the surface to 0.4 mm, and it was confirmed that the maximum diameter and the average diameter were the largest from the surface to a depth of 30 μm. Here, in the observation of carbides, those having an equivalent circle diameter of 0.5 μm or more can be identified as carbides.
The carbon concentration was measured by EPMA line analysis from the surface to a depth of 0.4 mm.
A rotating bending test and a roller pitching test were performed on each test piece after the carburization. First, the rotating bending fatigue test was carried out at a rotational speed of 3500 rpm and evaluated with a fatigue strength of 10 7 times. Further, the roller pitting test, the slip ratio of 40% was evaluated at 10 7 times strength under conditions of oil temperature 80 ° C. (limit strength pitching occurs in the test piece surface).
The obtained evaluation results are shown in Table 2.
表2に示したとおり、本発明に従う発明例はいずれも、冷間加工性に優れかつ耐疲労強度にも優れていることがわかる。 As shown in Table 2, it can be seen that all the inventive examples according to the present invention are excellent in cold workability and fatigue resistance.
Claims (3)
Si:0.01〜0.50質量%、
Mn:0.40〜1.50質量%、
P:0.02質量%以下、
S:0.03質量%以下、
Al:0.04〜0.10質量%、
Cr:0.5〜2.5質量%、
B:0.0005〜0.0050質量%、
Nb:0.003〜0.080質量%、
Ti:0.003質量%以下および
N:0.0080質量%未満
を含有し、残部はFe及び不可避不純物からなる成分組成を有する肌焼鋼に対して浸炭が施されてなる、浸炭材であって、表面から0.4mmまでの表層域における炭素量が0.85質量%以上であり、該表層域における、炭化物の最大径が10μm以下、かつ平均粒子径が4μm以下である浸炭材。 C: 0.10 to 0.35 mass%,
Si: 0.01 to 0.50 mass%,
Mn: 0.40-1.50 mass%,
P: 0.02 mass% or less,
S: 0.03 mass% or less,
Al: 0.04 to 0.10% by mass,
Cr: 0.5 to 2.5% by mass,
B: 0.0005-0.0050 mass%,
Nb: 0.003 to 0.080 mass%,
Ti: 0.003 mass% or less and N: less than 0.0080 mass%, and the balance is carburized material obtained by carburizing case- hardened steel having a component composition composed of Fe and inevitable impurities, from the surface A carburized material having a carbon content in a surface layer region of up to 0.4 mm of 0.85% by mass or more, a maximum carbide diameter of 10 μm or less, and an average particle size of 4 μm or less in the surface layer region .
Cu:1.0質量%以下、
Ni:0.50質量%以下、
Mo:0.50質量%以下および
V:0.5質量%以下
のうちから選ばれる1種または2種以上を含有する請求項1に記載の浸炭材。 The component composition further includes:
Cu: 1.0 mass% or less,
Ni: 0.50 mass% or less,
The carburized material according to claim 1, containing one or more selected from Mo: 0.50 mass% or less and V: 0.5 mass% or less.
Ca:0.0005〜0.0050質量%および
Mg:0.0002〜0.0020質量%
の1種または2種を含有する請求項1または2に記載の浸炭材。 The component composition further includes:
Ca: 0.0005 to 0.0050 mass% and
Mg: 0.0002 to 0.0020 mass%
The carburized material according to claim 1 or 2, comprising one or two of the following.
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