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A molecular dynamics simulation of pressure-driven gas permeation in a micropore potential field on silica membranes

机译:硅膜上微孔势场中压力驱动气体渗透的分子动力学模拟

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The mechanisms involved in pressure-driven gas permeation through a micropore on vitreous SiO_2 membranes were examined molecular dynamics (MD) simulation. Virtual amorphous SiO_2 membranes were prepared by the melt-quench method utilizing modified Born-Mayer-Huggins (BMH) pair potential and Stillinger-Weber (SW) three-body interactions. A dual control plane non-equilibrium MD (DCP-NEMD) technique was employed to simulate gas permeation phenomena under a constant upstream pressure, in which the permeating molecules were modeled as Lennard-Jones particles. The dependencies of the permeance of helium and CO_2 molecules on temperature and pore size were examined. For cylindrical pores about 8 and 6 A in diameter, the calculated temperature dependencies for the permeance of helium molecules were similar to the tendencies predicted by the normal Knudsen permeation mechanism, while in the case of CO_2 permeation, a temperature dependency larger than helium and a significant deviation from the Knudsen mechanism were observed. The deviation was more obvious for the smaller 6 A pore model. A simple gas permeation model that takes the effect of the pore wall potential field into consideration satisfactorily explained the permeation properties of CO_2 in the high temperature region. The permeation mechanism was also examined from the viewpoint of the lateral potential and density distribution in a micropore. The values for the potential within micropores, predicted from the observed temperature dependencies of the gas permeation rate and using the simple gas permeation model, were in good agreement with the depth of the potential field resulting from the given potential parameters. The findings also indicate that the density (pressure) difference in a micropore between the pore entrance and exit, which could be enhanced by an attractive pore wall potential, might be the true driving force for permeation, particularly in the high temperature region.
机译:通过分子动力学(MD)模拟研究了压力驱动的气体透过玻璃质SiO_2膜上的微孔渗透的机制。利用改良的Born-Mayer-Huggins(BMH)对势和Stillinger-Weber(SW)三体相互作用,通过熔体猝灭法制备了虚拟非晶态SiO_2膜。采用双控制平面非平衡MD(DCP-NEMD)技术来模拟恒定上游压力下的气体渗透现象,其中渗透分子被建模为Lennard-Jones粒子。研究了氦气和CO_2分子的磁导率对温度和孔径的依赖性。对于直径约为8和6 A的圆柱孔,计算得出的氦分子渗透率的温度依赖性与正常Knudsen渗透机理预测的趋势相似,而在CO_2渗透的情况下,温度依赖性大于氦气和观察到与努森机制的显着偏离。对于较小的6 A孔模型,偏差更明显。一个简单的气体渗透模型,充分考虑了孔壁势场的影响,可以令人满意地解释高温区域内CO_2的渗透特性。还从横向电位和微孔中的密度分布的角度检查了渗透机理。根据观察到的气体渗透速率的温度依赖性并使用简单的气体渗透模型预测的微孔内电势值,与给定电势参数所产生的电势深度高度吻合。这些发现还表明,孔的入口和出口之间的微孔密度(压力)差可以通过有吸引力的孔壁电势增强,这可能是渗透的真正驱动力,尤其是在高温区域。

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