分子动力学
硫酸盐
化学物理
化学
动力学(音乐)
计算化学
物理
有机化学
声学
作者
Cintia P. Lamas,Carlos Vega,Paola Gallo
标识
DOI:10.1080/00268976.2024.2406260
摘要
Ions significantly alter the water's structure, impacting properties such as the temperature of maximum density and the freezing point. We study structural changes in water upon adding sulfate anions, specifically Na2SO(4), K2SO4, Li2SO4, and MgSO4, using computer simulations. We employ the TIP4P/2005 water and the Madrid-2019 force field. By simulating solutions at various concentrations (0.64, 1.30, 1.90, and 3 mol kg(-1)) and two temperatures (300 and 240 K), we explore how these electrolytes disrupt water's structure and how they modify the interplay between Low Density Water and High Density Water. Increased salt concentration perturbed water's radial distribution functions (RDFs), particularly up to 240 K. Na2SO4 significantly disrupted water structure, reducing RDF peak heights and indicating decreased tetrahedrality, while MgSO4 increased structural order. K2SO4 displayed anomalous behaviour, minimally affecting water at 1.90 mol kg(-1) and ambient temperature but causing more ordered structures at 240 K. Orientational order parameter qt analysis supported these findings. Hydrogen bond network analysis showed notable perturbations at lower temperatures. Diffusion coefficients generally decreased with concentration, with K2SO4 exhibiting increase at 240 K. These results highlight the complex interactions between sulfate ions and water, enhancing our understanding of electrolyte solutions.[GRAPHICS].
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