JP7844937B2 - Method for manufacturing hot-forged materials - Google Patents
Method for manufacturing hot-forged materialsInfo
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Description
本発明は、熱間鍛造材の製造方法に関するものである。 This invention relates to a method for manufacturing hot-forged materials.
AMS6278で規定される合金は、M50NiLと呼ばれ、その組成は、質量%でC(炭素)が0.11~0.15%、Si(珪素)が0.10~0.25%、Mn(マンガン)が0.15~0.35%、Ni(ニッケル)が3.20~3.60%、Cr(クロム)が4.00~4.25%、Mo(モリブデン)が4.00~4.50%、V(バナジウム)が1.13~1.33%を含有し、残部がFe(鉄)および不純物からなる鋼である。このM50NiLは軸受鋼として、例えば、航空機のエンジン部品として用いられる。
このM50NiLの製造方法としては、例えば特許文献1に記されるように、棒状の被加工材を素材とし、所定の長さに切断され、鍛造、旋削などの加工が実施されることにより、所定の形状に加工が施される。
The alloy specified in AMS6278 is called M50NiL, and its composition, by mass%, is 0.11–0.15% C (carbon), 0.10–0.25% Si (silicon), 0.15–0.35% Mn (manganese), 3.20–3.60% Ni (nickel), 4.00–4.25% Cr (chromium), 4.00–4.50% Mo (molybdenum), and 1.13–1.33% V (vanadium), with the remainder being Fe (iron) and impurities. This M50NiL is used as bearing steel, for example, in aircraft engine components.
As for the manufacturing method of M50NiL, as described in Patent Document 1, for example, a rod-shaped workpiece is used as the raw material, cut to a predetermined length, and then processed into a predetermined shape by forging, turning, and other processes.
また本願出願人は特許文献2において、M50NiL相当合金の熱間鍛造工程における超音波探傷試験不良を防止することを目的とした熱間鍛造材の製造方法を提案している。この製造方法は、鍛造用素材を1000~1100℃の鍛造温度に加熱する鍛造温度加熱工程と、前記加熱した鍛造用素材をラジアル鍛造にて、鍛造用素材を周方向に回転しつつ、全長にわたって4方向から押圧することで全長を伸長する操作を繰り返して熱間鍛造材とする熱間鍛造工程と、を含み、前記熱間鍛造工程において、鍛造終了温度を800℃以上とするものである。 Furthermore, in Patent Document 2, the applicant has proposed a method for manufacturing hot-forged materials aimed at preventing defects in ultrasonic testing during the hot forging process of an alloy equivalent to M50NiL. This manufacturing method includes a forging temperature heating step in which the forging material is heated to a forging temperature of 1000 to 1100°C, and a hot forging step in which the heated forging material is subjected to radial forging, repeatedly extending its length by rotating it circumferentially and pressing it from four directions along its entire length, thereby producing a hot-forged material. In the hot forging step, the forging completion temperature is set to 800°C or higher.
上述したようなM50NiL製品の機械特性を低下させる要因の一つとして、結晶粒の粗大化が挙げられる。特に平均結晶粒度が小さくても、結晶粒が部分的に粗大化して粗大粒と微細粒とが混在した混粒組織となっている場合、粗大粒部を起因とした亀裂の発生が懸念されるため、最大結晶粒度も併せて小さくすることが重要である。このような最大結晶粒度を小さくすることについて上述した特許文献では検討されていない。特に特許文献2において超音波探傷試験不良(UT欠陥)の原因となる粗大な結晶粒の大きさは、結晶粒の長径で凡そ600μm以上であるところ、機械特性劣化を引き起こす粗大な結晶粒の大きさは例えば長径で200~400μm程度と、UT欠陥の原因となる粗大な結晶粒よりも小さい場合があり、超音波探傷試験で検知されない可能性がある。
よって本発明の目的は、M50NiL相当合金の熱間鍛造時および焼入れ後の結晶粒度のばらつきを抑制することが可能な熱間鍛造材の製造方法を提供することである。
One of the factors that degrades the mechanical properties of M50NiL products as described above is grain coarsening. In particular, even if the average grain size is small, if the grains are partially coarse and a mixed grain structure with both coarse and fine grains is formed, there is a concern that cracks may occur due to the coarse grains, so it is important to also reduce the maximum grain size. The aforementioned patent documents have not considered how to reduce the maximum grain size in this way. In particular, in Patent Document 2, the size of coarse grains that cause ultrasonic testing defects (UT defects) is approximately 600 μm or more in terms of the major axis of the grain, but the size of coarse grains that cause deterioration of mechanical properties may be smaller than the coarse grains that cause UT defects, for example, around 200 to 400 μm in terms of the major axis, and may not be detected by ultrasonic testing.
Therefore, the object of the present invention is to provide a method for producing a hot-forged material that can suppress variations in grain size during hot forging and after quenching of an alloy equivalent to M50NiL.
本発明は、上述した課題に鑑みてなされたものである。
すなわち本発明は、質量%でC:0.11~0.15%、Si:0.10~0.25%、Mn:0.15~0.35%、Cr:4.00~4.25%、Ni:3.20~3.60%、Mo:4.00~4.50%、V:1.13~1.33%、残部はFe及び不可避的不純物でなる鍛造用素材を準備する準備工程と、前記鍛造用素材を1070~1200℃の温度に加熱した後熱間鍛造して、仕上鍛造用素材を得る分塊工程と、前記仕上鍛造用素材を1100~1200℃の温度に加熱した後、前記加熱した仕上鍛造用素材をラジアル鍛造にて、仕上鍛造用素材を周方向に回転しつつ、全長にわたって4方向から押圧することで全長を伸長する操作を繰り返して熱間鍛造材とする仕上熱間鍛造工程とを含む、熱間鍛造材の製造方法である。
This invention was made in view of the above-mentioned problems.
In other words, the present invention comprises a preparation step of preparing a forging material consisting of, by mass%, C: 0.11-0.15%, Si: 0.10-0.25%, Mn: 0.15-0.35%, Cr: 4.00-4.25%, Ni: 3.20-3.60%, Mo: 4.00-4.50%, V: 1.13-1.33%, with the remainder being Fe and unavoidable impurities, and a step of heating the forging material to a temperature of 1070-1200°C. This method for manufacturing a hot-forged material includes a step of dividing the material into blocks to obtain a material for finish forging by hot forging, and a step of finishing hot forging in which the material for finish forging is heated to a temperature of 1100 to 1200°C, and then the heated material for finish forging is subjected to radial forging, in which the material is rotated in the circumferential direction and pressed from four directions along its entire length, thereby extending the overall length and producing a hot-forged material.
本発明によれば、M50NiL相当合金の熱間鍛造時および焼入れ後の結晶粒度のばらつきを抑制することが可能となる。 According to the present invention, it is possible to suppress variations in grain size during hot forging and after quenching of an alloy equivalent to M50NiL.
先ず、本発明で規定するM50NiL相当合金の組成限定理由について述べる。
C:0.11~0.15%
Cは硬さを向上させるのに有効な元素であり、最低0.11%を必要とするが、0.15%を超えるCの添加は靭性を低下させてしまうため、Cは0.11%~0.15%とする。
Si:0.10~0.25%
Siはフェライト相を強化するのに有効な元素である。Siが0.10%未満では、材料の延性が高すぎ、冷間での切削加工性を阻害してしまう。一方0.25%を超えるSiの添加は靭性を低下させてしまうため、Siは0.10%~0.25%とする。
Mn:0.15~0.35%
Mnは焼入性を向上させるのに有効な元素であり、最低0.15%を必要とする。一方、Mnが0.35質量%を超えると、硬度が上昇しすぎてしまい、加工性を悪くするといった問題が発生するため、Mnは0.15%~0.35%とする。
First, we will explain the reason for limiting the composition of the M50NiL equivalent alloy as defined in this invention.
C: 0.11-0.15%
Carbon (C) is an effective element for improving hardness, and a minimum of 0.11% is required. However, adding more than 0.15% of C reduces toughness, so the amount of C should be between 0.11% and 0.15%.
Si: 0.10~0.25%
Si is an effective element for strengthening the ferrite phase. If the Si content is less than 0.10%, the material becomes too ductile, hindering cold machinability. On the other hand, adding more than 0.25% Si reduces toughness, so the Si content should be between 0.10% and 0.25%.
Mn: 0.15-0.35%
Mn is an effective element for improving hardenability, and a minimum of 0.15% is required. On the other hand, if the amount of Mn exceeds 0.35% by mass, the hardness increases too much, causing problems such as poor machinability. Therefore, the amount of Mn should be between 0.15% and 0.35%.
Ni:3.20~3.60%
Niは焼入性を向上させるのに有効な元素であり、最低3.20%必要であるが、過度な添加はMs点が下がり残留オーステナイトが多くなり、冷間加工後の変形が多くなるといった問題が発生するため、Niは3.20~3.60%の範囲とする。
Cr:4.00~4.25%
Crは後述するするMoと同様、焼入性の向上、及び高温での焼戻し軟化抵抗を向上させる効果があるため最低4.00%の添加が必要である。一方、Crが4.25%を超えると、炭化物の析出が促進され、製造上での硬さの制御が困難となる。したがって、Crは4.00%~4.25%とする。
Ni: 3.20-3.60%
Ni is an effective element for improving hardenability, and a minimum of 3.20% is required. However, excessive addition lowers the Ms point, leading to an increase in retained austenite and problems such as increased deformation after cold working. Therefore, the Ni content should be in the range of 3.20% to 3.60%.
Cr: 4.00-4.25%
Similar to Mo (which will be discussed later), Cr has the effect of improving hardenability and resistance to tempering softening at high temperatures, so a minimum of 4.00% is necessary for its addition. On the other hand, if the Cr content exceeds 4.25%, carbide precipitation is promoted, making it difficult to control the hardness during manufacturing. Therefore, the Cr content should be between 4.00% and 4.25%.
Mo:4.00~4.50%
Moは焼入性と向上と高温での焼戻し軟化抵抗を向上させる効果があるため最低4.00%の添加が必要である。一方、Moが4.50%を超えると、炭化物の析出が促進され、製造上での硬さの制御が困難となる。したがって、Moは4.00%~4.50%とする。
V:1.13~1.33%
Vは焼戻し軟化抵抗を向上させる効果と結晶粒を細かくする効果がある。Vが1.13%未満では、VCの析出が少なく、結晶粒が粗大化する。一方、Vが1.33%を超えると、炭化物の析出が促進され、製造上での硬さの制御が困難となる。したがって、Vは1.13%~1.33%とする。
以上、説明する各元素の他は、Feと不可避的不純物である。
Mo: 4.00-4.50%
Mo is necessary at a minimum of 4.00% because it improves hardenability and resistance to tempering softening at high temperatures. On the other hand, if the amount of Mo exceeds 4.50%, carbide precipitation is promoted, making it difficult to control hardness during manufacturing. Therefore, the amount of Mo should be between 4.00% and 4.50%.
V: 1.13-1.33%
V has the effect of improving tempering softening resistance and refining the crystal grains. If V is less than 1.13%, VC precipitation is small and the crystal grains become coarser. On the other hand, if V exceeds 1.33%, carbide precipitation is promoted, making it difficult to control the hardness during manufacturing. Therefore, V should be set between 1.13% and 1.33%.
Besides the elements described above, the only other components are Fe and unavoidable impurities.
次に、本発明を製造工程の順に説明する。
<準備工程>
先ず、上記組成を有するM50NiL相当合金の鋼塊を製造する。上述のようにM50NiL相当合金は航空機のエンジン部品等に用いられる合金であるため、真空溶解で消耗電極を製造し、真空再溶解を行って非金属介在物の低減、成分偏析の低減を行うことが好ましい。本発明では鋼塊を鍛造用素材としてもよく、例えばさらに機械加工を行って丸棒状または角棒状の鍛造用素材としてもよい。なお、成分偏析を更に低減するため、鍛造用素材に均質化熱処理を行っても良い。
Next, the present invention will be described in the order of the manufacturing process.
<Preparation process>
First, a steel ingot of an M50NiL equivalent alloy having the above composition is manufactured. As mentioned above, since the M50NiL equivalent alloy is an alloy used in aircraft engine parts and the like, it is preferable to manufacture consumable electrodes by vacuum melting and then perform vacuum remelting to reduce nonmetallic inclusions and component segregation. In this invention, the steel ingot may also be used as a forging material, and for example, it may be further machined to form a round bar or square bar forging material. Furthermore, to further reduce component segregation, the forging material may be subjected to homogenization heat treatment.
<分塊工程>
前記鍛造用素材を1070~1200℃の鍛造温度に加熱した後、この鍛造温度(鍛造開始温度)で熱間鍛造する分塊工程を行う。上述した温度で分塊工程を実施することで、後述する仕上熱間鍛造工程と組み合わせて結晶粒が微細かつ均一な組織を得ることができる。加熱温度が1070℃未満となった場合、成長しきれていない微細結晶粒や粗大な未再結晶粒が残存した混粒組織となることにより、機械特性が低下する懸念がある。なお、本実施形態における「混粒」とは、1視野内において最大頻度を有する粒度番号と3以上異なったものが存在し、それが面積率で20%以上を占めたものを示す。加熱温度が1200℃を超える場合、結晶粒の過大な成長により粗大結晶粒が形成される懸念がある。なお本実施形態の分塊工程における「熱間鍛造」は、大きい鋼塊形状の加工を容易とするために、表面が平面または曲面である金敷の上に被加工材を載置し、同じく表面が平面または曲面であるハンマーにより材料を加工する熱間自由鍛造とすることができるが、金型を用いた型入鍛造でもよい。また、鍛造用素材を周方向に回転しつつ、全長にわたって4方向から押圧することで全長を伸長する操作を繰り返して鍛造材を得るラジアル鍛造を、上述した自由鍛造または型入鍛造と組み合わせて実施してもよい。また、分塊工程と仕上熱間鍛造工程との間に熱処理工程や研磨工程を導入することもできる。
<Bulking process>
After heating the forging material to a forging temperature of 1070 to 1200°C, a splitting process is performed in which hot forging is carried out at this forging temperature (forging start temperature). By performing the splitting process at the above temperature, a fine and uniform structure can be obtained in combination with the finishing hot forging process described later. If the heating temperature is below 1070°C, there is a concern that the mechanical properties will deteriorate due to the formation of a mixed-grain structure in which fine crystal grains that have not grown sufficiently and coarse, unrecrystallized grains remain. In this embodiment, "mixed grains" refers to grains in which there are grain size numbers that differ by 3 or more from the grain size number with the highest frequency within one field of view, and these grains account for 20% or more of the area. If the heating temperature exceeds 1200°C, there is a concern that coarse crystal grains will be formed due to excessive growth of the crystal grains. In this embodiment, the "hot forging" in the ingot-splitting process can be performed as free hot forging, in which the workpiece is placed on an anvil with a flat or curved surface and the material is processed with a hammer that also has a flat or curved surface, in order to facilitate the processing of large steel ingot shapes. However, die forging using a die may also be used. Furthermore, radial forging, in which the forging material is rotated circumferentially and pressed from four directions along its entire length to extend the overall length, may be performed in combination with the free forging or die forging described above. In addition, heat treatment and polishing processes can be introduced between the ingot-splitting process and the finish hot forging process.
<仕上熱間鍛造工程>
続いて前記分塊工程後の仕上鍛造用素材を、1100~1200℃の鍛造温度に加熱し、この鍛造温度(鍛造開始温度)によるラジアル鍛造にて熱間鍛造材(以下、「鍛造材」とも記載する)を得る、仕上熱間鍛造工程を実施する。仕上熱間鍛造工程においてラジアル鍛造を適用するのは、送り量・素材の回転量・素材への圧下量を高精度で制御しながら徐々に多角形に鍛造し、最終的には丸形状に加工することを可能にしている制御機構を利用することによって、加工発熱をコントロールし製品内部及び表面の温度制御を行なえるからである。本実施形態において加熱温度の下限を1100℃とした理由は、再結晶を促進させて結晶粒度のばらつきを小さくするためであり、加熱温度の上限を1200℃とした理由は、結晶粒の粗大化を抑制するためである。好ましい加熱温度の下限は1120℃である。
なお、ラジアル鍛造による鍛伸(鍛造)は、押圧による圧下を50~210回/分、1パス当たりの減面率を20~28%、前記被鍛造材の挿入側での送り速度を2.7~6m/分の範囲とするのがよい。この条件で鍛造することにより、全長に渡り均一な組織制御を可能にし、かつ加工発熱量の調整が容易なため、終了温度のコントロールを行なえる。そして、鍛造終了温度を800℃以上と設定できる。なお、鍛造終了温度を800℃以上にするためには、1パス当りの鍛造時間が短くなる条件で鍛造するとよい。鍛造終了温度が800℃未満となると、材料表層の温度が下がり、オーステナイト粒の再結晶が促進されないため、部分的に粗大な結晶粒が残存する。そのため、鍛伸終了温度は800℃以上とする。好ましい鍛伸終了温度は820℃以上である。なお、鍛造終了温度は鍛造材の表面温度である。以上説明する本発明の熱間鍛造材の製造方法によれば、熱間鍛造時および焼入れ後の結晶粒度のばらつきを防止することができる。
<Finishing Hot Forging Process>
Next, the material for finish forging after the mass separation process is heated to a forging temperature of 1100 to 1200°C, and a hot forged material (hereinafter also referred to as "forged material") is obtained by radial forging at this forging temperature (forging start temperature) in a finish hot forging process. Radial forging is applied in the finish hot forging process because by utilizing a control mechanism that enables the gradual forging into a polygon while precisely controlling the feed rate, material rotation rate, and reduction rate onto the material, and ultimately processing into a round shape, processing heat generation can be controlled and the temperature inside and on the surface of the product can be controlled. In this embodiment, the reason for setting the lower limit of the heating temperature to 1100°C is to promote recrystallization and reduce the variation in grain size, and the reason for setting the upper limit of the heating temperature to 1200°C is to suppress grain coarsening. The preferred lower limit of the heating temperature is 1120°C.
For radial forging, it is preferable to reduce the material by pressing 50 to 210 times per minute, reduce the surface area per pass by 20 to 28%, and feed rate on the insertion side of the material to be forged in the range of 2.7 to 6 m/min. Forging under these conditions enables uniform microstructure control over the entire length and allows for easy adjustment of the amount of heat generated during processing, thus enabling control of the final temperature. The final forging temperature can be set to 800°C or higher. To achieve a final forging temperature of 800°C or higher, it is preferable to forge under conditions that shorten the forging time per pass. If the final forging temperature is below 800°C, the temperature of the material surface drops, and the recrystallization of austenite grains is not promoted, resulting in the retention of partially coarse grains. Therefore, the final forging temperature should be 800°C or higher. A preferred final forging temperature is 820°C or higher. The final forging temperature is the surface temperature of the forged material. According to the method for manufacturing hot-forged materials of the present invention described above, it is possible to prevent variations in grain size during hot forging and after quenching.
(実施例1)
真空溶解で消耗電極を作製し、その後前記消耗電極を用いて真空再溶解を行ってM50NiL相当合金の鋼塊を得た。その後、熱間加工、機械加工を行って、直径320mm、全長2000mmの角棒状の鍛造用素材を得た。この鍛造用素材から、長さ15mmの模擬実験用素材を得た。組成を表1に示す。
(Example 1)
A consumable electrode was prepared by vacuum melting, and then a steel ingot of an M50NiL equivalent alloy was obtained by vacuum remelting using the consumable electrode. Subsequently, hot working and machining were performed to obtain a rectangular bar-shaped forging material with a diameter of 320 mm and a total length of 2000 mm. From this forging material, a 15 mm long material for a simulated experiment was obtained. The composition is shown in Table 1.
まず分塊工程の最適温度を確認するための実験を行った。上記の模擬実験用素材から圧縮試験用素材を採取し、分塊工程を模擬した圧縮試験を実施した。加工条件は塑性加工シミュレーションソフトを用いて、実際の工程で鋼塊から面積円相当径240mmの仕上鍛造用素材とした場合と同等の圧縮条件となるように素材を圧縮した。加工温度条件は1120℃、1100℃、1080℃、1060℃、1040℃の5条件とし、加工後の試料を光学顕微鏡で観察した。分塊模擬圧縮試験後の縦断面(圧縮面に直交する断面)のミクロ組織写真を図1に示す。なお図1(a)~(e)において、上段の観察倍率は100倍、下段の観察倍率は200倍である。圧縮温度が1070℃以上である試料は図1(a)~(c)に示すように、観察視野において全面再結晶組織であり、均一な組織であることを確認した。一方、圧縮温度1060℃である試料は図1(d)に示すように未再結晶粒(図1(d)のA)と再結晶初期の微細粒(図1(d)のB)が存在し、成長した結晶粒と混粒状態であった。圧縮温度1040℃である試料は図1(e)に示すように、粗大な未再結晶粒(図1(e)のA)の残存が確認された。 First, an experiment was conducted to confirm the optimal temperature for the mass separation process. Compression test material was taken from the simulated experimental material described above, and a compression test simulating the mass separation process was carried out. The processing conditions were determined using plastic deformation simulation software, and the material was compressed to be equivalent to the compression conditions when a steel ingot is processed into a finish forging material with an area circle equivalent diameter of 240 mm in the actual process. Five processing temperature conditions were used: 1120°C, 1100°C, 1080°C, 1060°C, and 1040°C. The processed samples were observed with an optical microscope. Figure 1 shows microstructural images of the longitudinal section (section perpendicular to the compression plane) after the simulated mass separation compression test. In Figures 1(a) to (e), the observation magnification in the upper section is 100x, and the observation magnification in the lower section is 200x. Samples with a compression temperature of 1070°C or higher showed a uniform structure with recrystallized tissue throughout the observation field, as shown in Figures 1(a) to (c). On the other hand, the sample compressed at 1060°C contained unrecrystallized grains (Figure 1(d)A) and fine grains in the early stages of recrystallization (Figure 1(d)B), as shown in Figure 1(d), and was in a mixed state with grown crystal grains. The sample compressed at 1040°C, as shown in Figure 1(e), showed the presence of coarse unrecrystallized grains (Figure 1(e)A).
(実施例2)
次に仕上熱間鍛造工程の最適温度を確認するための実験を行った。実施例1と同じ模擬実験用素材から圧縮試験用素材を採取し、仕上熱間鍛造工程を模擬した圧縮試験を実施した。加工条件は塑性加工シミュレーションソフトを用いて、実工程で面積円相当径240mmの仕上鍛造用素材から、面積円相当径で140mmの鍛造材とした場合と同等の圧縮条件となるように素材を圧縮した。加工温度条件は1150℃(試料No.1)、1130℃(試料No.2)、1100℃(試料No.3)、1070℃(試料No.4)、1050℃(試料No.5)、1000℃(試料No.6)の6条件とし、加工後の試料を光学顕微鏡で観察した。また、鍛造後に実施する焼入れ処理後の結晶粒度への影響を確認するため、圧縮試験後の試料に焼なまし処理と焼入れ処理を実施した。なお、焼入れ処理後の結晶粒度は光学顕微鏡により倍率200倍、観察視野30視野の条件で観察し、画像解析ソフトウェアを用いて導出した。仕上模擬圧縮試験後の縦断面のミクロ組織写真を図2(上段の観察倍率:100倍、下段の観察倍率:200倍)に示す。また、仕上模擬圧縮試験後、焼なまし処理および1100℃×15minの焼入れ処理を実施した後の縦断面のミクロ組織写真を図3(上段の観察倍率:100倍、下段の観察倍率:200倍)、画像解析により測定した結晶粒度測定結果(平均結晶粒度と最大結晶粒度)を表2に示す。図2より、圧縮温度1050℃以上の試料No.1~5では全面再結晶組織であり、圧縮温度が高いほど微細な結晶粒が減少して結晶粒サイズが均一になる傾向であることを確認した。対して圧縮温度1000℃の試料No.6では未再結晶粒と微細な結晶粒が混在していた。そして図3および表2より、いずれの試料も平均結晶粒度は同等水準であるが、圧縮温度1100℃以上の試料No.1~3では、最大結晶粒が小さく、結晶粒度のばらつきが小さくなっていることを確認した。
(Example 2)
Next, an experiment was conducted to confirm the optimal temperature for the finish hot forging process. Compression test material was taken from the same simulated experimental material as in Example 1, and a compression test simulating the finish hot forging process was carried out. The processing conditions were determined using plastic deformation simulation software, and the material was compressed to the same compression conditions as when a finish forging material with an area circle equivalent diameter of 240 mm is made into a forging material with an area circle equivalent diameter of 140 mm in the actual process. Six processing temperature conditions were used: 1150°C (Sample No. 1), 1130°C (Sample No. 2), 1100°C (Sample No. 3), 1070°C (Sample No. 4), 1050°C (Sample No. 5), and 1000°C (Sample No. 6). The processed samples were observed with an optical microscope. In addition, to confirm the effect on the grain size after the quenching treatment performed after forging, annealing and quenching treatments were performed on the samples after the compression test. The grain size after quenching was observed using an optical microscope at a magnification of 200x and a field of view of 30, and derived using image analysis software. Figure 2 shows microstructure images of the longitudinal section after the finish simulation compression test (upper row: 100x magnification, lower row: 200x magnification). Figure 3 shows microstructure images of the longitudinal section after annealing and quenching at 1100°C for 15 min following the finish simulation compression test (upper row: 100x magnification, lower row: 200x magnification), and Table 2 shows the grain size measurement results (average grain size and maximum grain size) measured by image analysis. From Figure 2, it can be seen that samples No. 1 to 5, compressed at temperatures of 1050°C or higher, had a completely recrystallized structure, confirming that the higher the compression temperature, the fewer fine grains there were and the more uniform the grain size tended to be. In contrast, sample No. 6, compressed at 1000°C, had a mixture of unrecrystallized grains and fine grains. Furthermore, as shown in Figure 3 and Table 2, while the average grain size of all samples is at a similar level, it was confirmed that in samples No. 1 to 3, where the compression temperature was 1100°C or higher, the maximum grain size was smaller and the variation in grain size was reduced.
(実施例3)
実施例1および実施例2で加工温度が結晶粒度に与える影響が確認できたが、実施例1および実施例2は模擬実験であり、試料サイズが小さく、実際の鍛造材と比較して加熱ムラや歪による影響が少ない。そこで仕上熱間鍛造工程での加熱温度の影響を実際の製造工程で確認した。実施例1で用いたものと同じM50NiL相当合金の鋼塊に1100℃で熱間自由鍛造を行う分塊加工を実施し、直径140mm、全長3000mmの丸棒状の仕上鍛造用素材(本発明例の仕上鍛造用素材)と面積円相当径240mm、全長3000mmの角棒状の鍛造用素材(比較例の仕上鍛造用素材)を得た。本発明例の仕上鍛造用素材は1150℃に加熱しながら直径80mmまでラジアル鍛造して本発明例の鍛造材とし、比較例の仕上鍛造用素材は1050℃に加熱しながら直径140mmまでラジアル鍛造し、それぞれ鍛造材を得た。ここで本発明例と比較例とは、実体鍛錬成形比が同等となるように仕上熱間鍛造を実施した。その他の熱間鍛造条件は、本発明例及び比較例共に、押圧による圧下を75~105回/分、1パス当たりの減面率を25~30%、前記被鍛造材の挿入側での送り速度を4~5.5m/分の範囲とした。
得られた本発明例および比較例の鍛造材から試験片を採取して、光学顕微鏡で観察した結果を図4(上段:観察倍率200倍、下段:観察倍率500倍)に示す。試料の採取箇所について、径方向は鍛造材の表面から軸心方向に深さD/4(D:面積円相当径の直径)の位置、長さ方向は柱状鍛造材の頂部、中心部、底部の三か所とした。図4より、比較例では鍛伸方向に伸長した粗大な未再結晶粒が確認された。一方、本発明では結晶粒サイズが微細かつ均一な等軸の結晶粒組織であった。鍛造後の各素材を焼なまし処理と焼入れ処理を実施し、ASTM規格に従って光学顕微鏡により結晶粒度を測定した結果を図5に示す。観察方法は実施例2と同じである。図5より本発明例の鍛造材は、平均結晶粒度は比較例の鍛造材と同水準であるが、最大結晶粒度が比較例の鍛造材よりも微細化していた。以上の結果より、本発明で規定する熱間鍛造工程を適用することで、M50NiL相当合金の熱間鍛造時および焼入れ後の結晶粒度のばらつきを防止することが可能であることを確認した。
(Example 3)
In Examples 1 and 2, the effect of processing temperature on grain size was confirmed. However, Examples 1 and 2 were simulated experiments, and the sample size was small, resulting in less influence from uneven heating and distortion compared to actual forged materials. Therefore, the effect of heating temperature in the finishing hot forging process was confirmed in an actual manufacturing process. A block processing was performed on a steel ingot of the same M50NiL equivalent alloy used in Example 1, using hot free forging at 1100°C. This yielded a round bar-shaped finishing forging material with a diameter of 140 mm and a total length of 3000 mm (the finishing forging material of the present invention example) and a square bar-shaped forging material with an area circle equivalent diameter of 240 mm and a total length of 3000 mm (the finishing forging material of the comparative example). The material for finishing forging in the present invention example was radially forged to a diameter of 80 mm while being heated to 1150°C to obtain the forged material of the present invention example, and the material for finishing forging in the comparative example was radially forged to a diameter of 140 mm while being heated to 1050°C to obtain the forged material of the comparative example. Here, the finishing hot forging was carried out in the present invention example and the comparative example so that the actual forging ratio was the same. Other hot forging conditions for both the present invention example and the comparative example were set to a reduction by pressing of 75 to 105 times/min, a reduction ratio per pass of 25 to 30%, and a feed rate on the insertion side of the material to be forged in the range of 4 to 5.5 m/min.
Figure 4 (upper panel: 200x magnification, lower panel: 500x magnification) shows the results of observing test specimens taken from the forged materials of the present invention example and comparative example using an optical microscope. Regarding the sampling locations, in the radial direction, samples were taken at a depth D/4 (D: diameter of the area circle equivalent diameter) from the surface of the forged material axially, and in the longitudinal direction, samples were taken at three locations: the top, center, and bottom of the columnar forged material. Figure 4 shows that in the comparative example, coarse, unrecrystallized grains elongated in the forging direction were observed. On the other hand, in the present invention, the crystal grain size was fine and uniform, resulting in an equiaxed crystal grain structure. Each material after forging underwent annealing and quenching treatments, and the crystal grain size was measured using an optical microscope according to ASTM standards. Figure 5 shows the results. The observation method was the same as in Example 2. Figure 5 shows that the average crystal grain size of the forged material of the present invention example was at the same level as the forged material of the comparative example, but the maximum crystal grain size was finer than that of the forged material of the comparative example. Based on the above results, it was confirmed that applying the hot forging process defined in this invention makes it possible to prevent variations in grain size during hot forging and after quenching of an alloy equivalent to M50NiL.
Claims (1)
前記鍛造用素材を1070~1200℃の温度に加熱した後熱間鍛造して、仕上鍛造用素材を得る分塊工程と、
前記仕上鍛造用素材を1100~1200℃の温度に加熱した後、前記加熱した仕上鍛造用素材をラジアル鍛造にて、仕上鍛造用素材を周方向に回転しつつ、全長にわたって4方向から押圧することで全長を伸長する操作を繰り返して熱間鍛造材とする仕上熱間鍛造工程とを含む、熱間鍛造材の製造方法。
A preparation step to prepare a forging material consisting of, by mass%, C: 0.11-0.15%, Si: 0.10-0.25%, Mn: 0.15-0.35%, Cr: 4.00-4.25%, Ni: 3.20-3.60%, Mo: 4.00-4.50%, V: 1.13-1.33%, with the remainder being Fe and unavoidable impurities,
The process involves heating the forging material to a temperature of 1070 to 1200°C and then hot forging it to obtain a material for finishing forging, and
A method for manufacturing a hot forged material, comprising: heating the aforementioned finishing forging material to a temperature of 1100 to 1200°C; and then, in a finishing hot forging step, repeatedly performing radial forging on the heated finishing forging material, in which the finishing forging material is rotated circumferentially and pressed from four directions along its entire length to extend its overall length, thereby producing a hot forged material.
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