Molecular dynamics of deformation and fragmentation processes in liquid droplets under pulsed electric field

IF 2 3区 化学 Q4 CHEMISTRY, PHYSICAL Chemical Physics Pub Date : 2024-11-12 DOI:10.1016/j.chemphys.2024.112519
Chuanke Liang, Zexin Liu, Yeqi Yan, Yancheng Tao, Tao Li, Hailong Chen
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Abstract

The deformation and breakup of droplets are widely observed in various aspects of production and daily life. Using molecular dynamics simulations, this study primarily investigated the deformation and breakup of droplets in a nitrogen environment under pulsed electric fields of different frequencies. The results indicate that the droplet deformation undergoes periodic changes under the influence of the pulsed electric field. At equivalent electric field strengths, droplets are more likely to break under a 6.25 GHz pulsed electric field compared to a 25 GHz pulsed electric field, where droplet deformation remains stable without breaking. At every frequency, the bond energy of water molecules consistently decreases. The solvent-accessible surface area changes with the electric field at 6.25 GHz. Furthermore, the minimum value of hydrogen bond quantity reached under high-frequency pulsed fields is higher than that under low-frequency fields. The change in hydrogen bond quantity is inversely proportional to the solvent-accessible surface area. These findings provide insights into the microscopic mechanisms of droplet deformation and breakup, offering a reference for future studies.
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脉冲电场下液滴变形和破碎过程的分子动力学
液滴的变形和破裂广泛存在于生产和日常生活的各个方面。本研究利用分子动力学模拟,主要研究了不同频率脉冲电场作用下氮气环境中液滴的变形和破裂。结果表明,液滴变形在脉冲电场的影响下会发生周期性变化。在同等电场强度下,液滴在 6.25 GHz 脉冲电场下更容易断裂,而在 25 GHz 脉冲电场下,液滴变形保持稳定而不会断裂。在每个频率下,水分子的键能都会持续降低。在 6.25 GHz 频率下,可溶解表面积随电场变化而变化。此外,高频脉冲电场下氢键量达到的最小值高于低频电场下的最小值。氢键量的变化与可溶解表面积成反比。这些发现深入揭示了液滴变形和破裂的微观机理,为今后的研究提供了参考。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
Chemical Physics
Chemical Physics 化学-物理:原子、分子和化学物理
CiteScore
4.60
自引率
4.30%
发文量
278
审稿时长
39 days
期刊介绍: Chemical Physics publishes experimental and theoretical papers on all aspects of chemical physics. In this journal, experiments are related to theory, and in turn theoretical papers are related to present or future experiments. Subjects covered include: spectroscopy and molecular structure, interacting systems, relaxation phenomena, biological systems, materials, fundamental problems in molecular reactivity, molecular quantum theory and statistical mechanics. Computational chemistry studies of routine character are not appropriate for this journal.
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