分手
聚结(物理)
电场
化学物理
分子动力学
变形(气象学)
介观物理学
材料科学
分子
相(物质)
化学
场强
机械
计算化学
凝聚态物理
复合材料
物理
磁场
天体生物学
量子力学
有机化学
作者
Ning Li,Zhiqian Sun,Wenchuan Liu,Luchen Wei,Bin Li,Zhuang Qi,Zhenbo Wang
标识
DOI:10.1016/j.molliq.2021.115995
摘要
Electrostatic demulsification process is frequently accompanied by the occurrence of droplet breakup, which will cause a fall in the efficiency of droplet electro-coalescence. To uncover mechanisms of droplet deformation and breakup in the water-in-oil (W/O) emulsion, molecular dynamics simulations were used here to investigate the influence of electric field strength on the motion behavior of a single droplet. The results showed that with increasing field strengths, the droplet underwent deformation, breakup at one end, breakup at both ends, and breakup in the middle part, respectively, which is consistent with the experimental findings at mesoscopic scales. Quantum chemical calculations and noncovalent interaction analysis found that non-bonded potential energies between water molecules played a dominant role in droplet morphology transformation, supporting the reasonableness for gas-phase molecules instead of oil-phase molecules. Besides deformation ratio (Dr), solvent accessible surface area (SASA) is also an important parameter for characterizing the degree of droplet deformation at the molecular level. Electrostatic attraction among water molecules and external electric field force were found to be the key factors affecting droplet deformation. At field strength of 1.4 V nm−1, the majority of the hydrogen bonds between H2O had a very brief lifetime, 0.79 ps. Hydrated ions and ion migration perform critical roles during droplet breakup. This study fills an important gap in the molecular dynamics study of electrostatic coalescence by introducing real oil molecules.
科研通智能强力驱动
Strongly Powered by AbleSci AI