M. J. Aguila, Joshua P. Gemperoso, King Bryan C. Gabog, A. Magsino
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引用次数: 0
摘要
深共晶溶剂(DESs)被认为是化学和物理过程中较好的替代溶剂。对尿素和酒石酸钾钠二元混合物进行了研究。共晶体系由33%酒石酸钾钠和67%尿素(1:2摩尔比)组成。该共晶体系的凝固点为19.83±0.76℃,密度为1.1971±0.0003 g mL-1,粘度为34.4226±0.0665 cP。通过密度函数计算确定了尿素和酒石酸钾钠加合物与水分子的最稳定构象。加合物的气相总能为-5576863 kJ mol-1。阳离子和羧酸盐位点之间存在静电相互作用,尿素的质子和酒石酸盐的羟基氧之间存在h键,酒石酸盐的羟基和羧酸盐位点之间存在分子内h键。与非键相互作用相关的总能量计算为-826 kJ mol-1,这表明这些相互作用稳定了酒石酸钾钠和尿素的DES体系的形成。
Eutectic System Based on Urea and Potassium Sodium Tartrate
Deep eutectic solvents (DESs) are considered as better alternative solvents in chemical and physical processes. The binary mixture of urea and potassium sodium tartrate is explored in this study. A eutectic system is determined at composition made up of 33% potassium sodium tartrate and 67% urea (1:2 molar ratio). This eutectic system has a freezing point of 19.83 ± 0.76 °C, density of 1.1971 ± 0.0003 g mL-1, and viscosity of 34.4226 ± 0.0665 cP. The most stable conformation for the adduct of urea and potassium sodium tartrate with water molecules was determined through density functional calculations. The gas phase total energy for the adduct was determined as -5576863 kJ mol-1. Electrostatic interactions between the cations and the carboxylate sites are present, H-bonding between protons of urea and the hydroxyl oxygen of the tartrate, and intramolecular H-bonding between the hydroxyl and carboxylate sites of tartrate are accounted in the structure. The total energy associated with nonbonding interactions is computed as -826 kJ mol-1, which suggests that these interactions stabilize the formation of the DES system of potassium sodium tartrate and urea.