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Analyses of Transformation Kinetics of Carbide-Free Bainite Above and Below the Athermal Martensite-Start Temperature

机译:无马氏体起始温度以上和以下的无碳化物贝氏体的转变动力学分析

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The isothermal transformation kinetics of austenite decomposition in Fe-0.4C-2.78Mn-1.81Si was analyzed by an electrical resistivity technique in the temperature interval 723 K to 418 K (450 °C to 145 °C). The analysis of transformation kinetics of the bainite transformation was performed using the Johnson–Mehl–Avrami–Kolgomorov (JMAK) and Austin–Rickett (AR) approaches. The kinetic parameters, the reaction constant n, rate constant k = k(T), and apparent activation energy Q were evaluated for isothermal transformations below and above the martensite-start temperature M S = 548 K (275 °C), which was determined experimentally. The formation of strain-induced martensite, which starts to accompany the bainite transformation at just above M S , increases the rate of transformation and decreases the apparent activation energy of austenite decomposition.
机译:通过电阻率技术在723 K至418 K(450°C至145°C)的温度范围内分析了Fe-0.4C-2.78Mn-1.81Si中奥氏体分解的等温转变动力学。使用Johnson-Mehl-Avrami-Kolgomorov(JMAK)和Austin-Rickett(AR)方法进行贝氏体转变的转变动力学分析。在马氏体起始温度M S = 548 K之上和之上,针对等温转变评估了动力学参数,反应常数n,速率常数k = k(T)和表观活化能Q。 °C),这是通过实验确定的。应变诱发的马氏体的形成开始伴随贝氏体转变,刚好在M S 之上,从而增加了转变速率并降低了奥氏体分解的表观活化能。

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