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Effects of Molecular Chain Length on the Contact Line Movement in Water-Alkane/Solid Systems

机译:分子链长对水/正构烷烃/固体体系中接触线运动的影响

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摘要

The movement of the contact line in liquid-liquid-solid systems is a major phenomenon in natural and industrial processes. In particular, -alkanes are widely occurring in the oil, soil pollution, and chemical industries, yet there is little knowledge on the effects of molecular chain length on the contact line movement. Here, we studied the effects of molecular chain length on the contact line movement in water/ -alkane/solid systems with different surface wettabilities. We used -heptane (C ), -decane (C ), and -hexadecane (C ) as alkanes and -quartz as the solid surface. We calculated the time-variation contact line moving velocity and also analyzed the jump frequency and the mean distance of the molecular displacement occurring within the contact line zone by molecular-kinetic theory. Molecular dynamics simulation results show that the contact line velocity decreases with increasing the chain length, originally caused by the decreasing the jump frequency and mean distance. These variations with the molecular chain length are related to the more torsions and deformations of the molecules with a longer chain length. In addition, the moving mechanism of the contact line on the same solid surface does not change at different molecular chain lengths, implying that the moving mechanism mainly depends on the three-phase wettability.
机译:液-液-固系统中接触线的运动是自然和工业过程中的主要现象。特别是,-烷烃广泛应用于石油,土壤污染和化学工业,但对分子链长度对接触线运动的影响知之甚少。在这里,我们研究了分子链长度对具有不同表面润湿性的水/烷烃/固体体系中接触线运动的影响。我们使用-庚烷(C),-癸烷(C)和-十六烷(C)作为烷烃,并使用-石英作为固体表面。我们通过分子动力学理论计算了时变接触线的移动速度,并分析了在接触线区内发生的分子位移的跳跃频率和平均距离。分子动力学模拟结果表明,接触线速度随链长的增加而降低,这主要是由于跳跃频率和平均距离的降低所致。分子链长的这些变化与链长较长的分子的更多扭曲和变形有关。另外,同一固体表面上的接触线的移动机理在不同的分子链长度上没有变化,这意味着该移动机理主要取决于三相的润湿性。

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