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乙腈 - 水混合物的结构与动力学见解:自扩散、重取向相关时间及温度依赖性行为的分子动力学研究

Structural and Dynamical Insights into Acetonitrile-Water Mixtures: A Molecular Dynamics Study of Self-Diffusion, Reorientational Correlation Times, and Temperature-Dependent Behavior.

作者信息

Bouazizi Salah, Ayachi Sahbi, Nasr Salah

机构信息

Laboratory of Advanced Multifunctional Materials and Technological Applications (LR24ES04), Faculty of Sciences and Technologies of SidiBouzid, University of Kairouan, Kairouan 3100, Tunisia.

Laboratory of Physico-Chemistry of Materials (LR01ES19), Faculty of Sciences, University of Monastir, Avenue of the Environment, Monastir 5019, Tunisia.

出版信息

ACS Omega. 2025 Aug 15;10(33):38092-38102. doi: 10.1021/acsomega.5c05444. eCollection 2025 Aug 26.

Abstract

The study investigates the structural and dynamical properties of acetonitrile-water mixtures using molecular dynamics simulations over a broad range of acetonitrile molar fractions (0.0 to 1.0) and temperatures (298-348 K). The dielectric constant, recognized as one of the slowest-converging dynamical properties, exhibited consistent stabilization across all systems after approximately 20 ns. Particular attention is given to the self-diffusion coefficients and reorientational correlation times of key molecular vectors in both solvents. Structural analysis based on radial distribution functions reveals that the nearest neighbor interactions between acetonitrile molecules occur within the 2.85-4.00 Å range. With increasing acetonitrile concentration, the self-diffusion coefficient of acetonitrile increases progressively, whereas that of water exhibits a nonlinear dependence on the acetonitrile content. Reorientational correlation times for the OH and dipole moment vectors of water molecules exhibit nonlinear trends as a function of acetonitrile molar fraction, whereas the correlation time for the acetonitrile dipole moment decreases progressively with increasing acetonitrile concentrations. For all systems, self-diffusion coefficients increase with temperature, while reorientational correlation times decrease. In these mixtures, water molecules undergo reorientation via a jump rotation mechanism.

摘要

该研究通过分子动力学模拟,在广泛的乙腈摩尔分数(0.0至1.0)和温度范围(298 - 348 K)内,研究了乙腈 - 水混合物的结构和动力学性质。介电常数被认为是收敛最慢的动力学性质之一,在大约20纳秒后,所有系统中的介电常数都呈现出一致的稳定状态。特别关注了两种溶剂中关键分子矢量的自扩散系数和重取向相关时间。基于径向分布函数的结构分析表明,乙腈分子之间的最近邻相互作用发生在2.85 - 4.00 Å范围内。随着乙腈浓度的增加,乙腈的自扩散系数逐渐增大,而水的自扩散系数对乙腈含量呈现非线性依赖关系。水分子的OH和偶极矩矢量的重取向相关时间随乙腈摩尔分数呈现非线性趋势,而乙腈偶极矩的相关时间随着乙腈浓度的增加而逐渐减小。对于所有系统,自扩散系数随温度升高而增大,而重取向相关时间则减小。在这些混合物中,水分子通过跳跃旋转机制进行重取向。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b115/12392041/fcb601951518/ao5c05444_0001.jpg

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