简介概要

连续升温过程中γ-Fe→δ-Fe→液态Fe相变的分子动力学模拟

来源期刊:金属学报2010年第2期

论文作者:刘益虎 吴永全 沈通 王召柯 蒋国昌

文章页码:172 - 178

关键词:纯Fe; 升温相变; 分子动力学; 微观结构

Key words:pure Fe; temperature-rise phase transition; molecular dynamics; microstructure

摘    要:采用所构建的长程F-S势函数,对连续升温过程中γ-Fe→δ-Fe→液态Fe的相变过程进行了分子动力学(MD)模拟。结果表明,计算得到的γ-Fe,δ-Fe以及液态Fe的微观结构(径向分布函数、配位数)和宏观物性(密度)都能与实验结果吻合很好,但相变温度点与实验值的偏差较大,推测是由过快升温速度造成的过热度过高所致,从微观结构、瞬态能量及密度的分析出发,讨论了固态相变(γ-Fe→δ-Fe)和固-液相变(δ-Fe→液态Fe)的具体过程,其中,固态相变主要形成于晶格扭曲和滑移,而固-液相变即熔化过程起始于固体岛颗粒的边缘,并逐渐向其中心扩散,在相变演化过程中,通过瞬态能量和密度的起伏观察到明显的孕育过程。

Abstract: Understanding high-temperature phase transformations of pure Fe is fundamental for quality control and product design of steels.Various theoretical methods have been used to determine dynamically the mechanism of phase transformations in pure Fe including γ-Fe to δ-Fe and δ-Fe to liquid-Fe.Among these methods,molecular dynamics(MD) simulation has become a prospective method,in which atomic interactions play a key role in phase transformations.However,most attention was focused on the MD simulation of temperature-drop phase transformations rather than temperature-rise phase transformations before.In the present study the isothermal-isobaric MD simulation at a wide temperature range of γ-Fe→δ-Fe→liquid-Fe transformations in pure Fe was carried out by giving a set of long-range Finnis-Sinclair potential parameters.The results show that a better agreement between simulation and experimental results for the microstructures(including radial distribution functions and coordination numbers) and densities of transformed phases validate that the set of potential parameters for the MD simulation are reasonable.The larger difference between the calculated and experimental transformation temperatures is attributed to the effect of superheat degree induced by ultrafast heating speed in the MD simulation.Evolvement of microstructures exhibits lattice-distorting and sliding induced by γ-Fe to δ-Fe phase transformation and melting of δ-Fe islands from δ-Fe to liquid Fe.Finally,in the MD simulation stronger and stronger fluctuations of instantaneous energy and density just before transformations,especially melting,show an apparent pregnant process in phase transformations.

详情信息展示

连续升温过程中γ-Fe→δ-Fe→液态Fe相变的分子动力学模拟

刘益虎1,吴永全2,沈通2,王召柯2,蒋国昌2

(1.上海市上海大学上海市现代冶金与材料制备重点实验室
2.上海大学 上海市现代冶金及材料制备重点实验室)

摘 要:采用所构建的长程F-S势函数,对连续升温过程中γ-Fe→δ-Fe→液态Fe的相变过程进行了分子动力学(MD)模拟。结果表明,计算得到的γ-Fe,δ-Fe以及液态Fe的微观结构(径向分布函数、配位数)和宏观物性(密度)都能与实验结果吻合很好,但相变温度点与实验值的偏差较大,推测是由过快升温速度造成的过热度过高所致,从微观结构、瞬态能量及密度的分析出发,讨论了固态相变(γ-Fe→δ-Fe)和固-液相变(δ-Fe→液态Fe)的具体过程,其中,固态相变主要形成于晶格扭曲和滑移,而固-液相变即熔化过程起始于固体岛颗粒的边缘,并逐渐向其中心扩散,在相变演化过程中,通过瞬态能量和密度的起伏观察到明显的孕育过程。

关键词:纯Fe; 升温相变; 分子动力学; 微观结构

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