Under pressure: Quasi-high pressure effects in nanopores

被引:46
|
作者
Long, Yun [1 ]
Palmer, Jeremy C. [1 ]
Coasne, Benoit [2 ]
Sliwinska-Bartkowiak, Malgorzata [3 ]
Gubbins, Keith E. [1 ]
机构
[1] N Carolina State Univ, Dept Chem & Biomol Engn, Raleigh, NC 27695 USA
[2] Univ Montpellier 2, Inst Charles Gehardt Monpellier, CNRS UMR 5253, F-34296 Montpellier, France
[3] Adam Mickiewicz Univ, Inst Phys, PL-61614 Poznan, Poland
基金
美国国家科学基金会;
关键词
Molecular simulation; Pressure tensor; Adsorption; Pressure enhancement; MOLECULARLY THIN-LAYERS; ELASTIC-CONSTANTS; CONFINEMENT; LIQUIDS; DIMERIZATION; BEHAVIOR; SURFACE; TENSOR; FLUIDS; NO;
D O I
10.1016/j.micromeso.2011.07.017
中图分类号
O69 [应用化学];
学科分类号
081704 ;
摘要
Phenomena that occur only at high pressures in bulk phases are often observed in nanopores, suggesting that the pressure in such confined phases is large. We develop two models to study the pressure tensor of an argon nanophase confined in carbon micropores by molecular simulation, and show that the in-pore tangential pressure is positive and on the order of 10(4) bar, while the normal pressure can be positive or negative depending on pore width, with a magnitude of similar to 10(3) bar at ambient bulk pressure. We find that the in-pore tangential pressure is very sensitive to the bulk pressure, suggesting that it should be possible to control the former over wide ranges in laboratory experiments. We also report results for porous materials other than carbon, and show that the pressure enhancement is smaller for pores with weakly attractive walls (e.g. silica and oxides), but larger for more strongly attractive walls (e.g. mica). (C) 2011 Elsevier Inc. All rights reserved.
引用
收藏
页码:19 / 23
页数:5
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