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Interplay of vapor adsorption and liquid imbibition in nanoporous Vycor glass

机译:纳米多孔Vycor玻璃中蒸气吸附和液体吸收的相互作用

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We have studied the kinetics of spontaneous capillary rise and of the concurrent vapor adsorption in nanoporous, monolithic samples of Vycor glass with a mean pore diameter of 7.5 nm. As liquids, we have chosen n-alcohols (n = 4-10) whose vapor pressures at room temperature range from p(0) = 965 Pa down to p(0) = 0.743 Pa. Dielectric measurements allow us to achieve spatial selectivity to predefined parts of the porous Vycor glass. In this way, we are able to measure the overall uptake of molecules as well as vapor adsorption from the surroundings in unfilled parts of the pore network, i.e., above the liquid menisci of the rising imbibition front. We show that the latter process is unaltered compared to free adsorption in samples suspended above a liquid reservoir. Only at low vapor pressures, i.e., for long alcohols, vapor adsorption can be neglected and the capillary rise follows the theoretical predictions of the Lucas-Washburn root t law. The more volatile the alcohol, the more important the additional adsorption of molecules becomes. We show that the overall filling process in the pore network is well described by a superposition of the Lucas-Washburn law and the measured vapor adsorption. In addition, the experiments give insight into the vapor diffusion dynamics in the porous matrix.
机译:我们研究了平均孔径为7.5 nm的Vycor玻璃纳米多孔,整体样品中自发毛细管上升和同时发生的蒸气吸附的动力学。作为液体,我们选择了n-醇(n = 4-10),其在室温下的蒸气压范围从p(0)= 965 Pa下降到p(0)= 0.743 Pa。介电测量使我们能够实现对Vycor多孔玻璃的预定义部分。通过这种方式,我们能够测量分子的总体吸收以及在孔隙网络未填充部分(即在上升的吸水前沿的液体弯液面上方)从周围环境中吸收的蒸气。我们表明,与悬浮在储液罐上方的样品中的自由吸附相比,后一过程没有改变。仅在低蒸气压下,即对于长醇,才可以忽略蒸气吸附,并且毛细管上升遵循Lucas-Washburn根定律的理论预测。醇的挥发性越大,分子的额外吸附就变得越重要。我们表明,通过Lucas-Washburn定律和测得的蒸气吸附的叠加可以很好地描述孔隙网络中的整个填充过程。此外,实验还可以洞察多孔基质中的蒸汽扩散动力学。

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