Thermodynamic stability of clathrate hydrates relative to their separate chemical components

被引:5
|
作者
White, MA [1 ]
MacLaren, DC
Marriott, RA
Zhan, BZ
机构
[1] Dalhousie Univ, Dept Chem, Halifax, NS B3H 4J3, Canada
[2] Dalhousie Univ, Mat Res Inst, Halifax, NS B3H 4J3, Canada
关键词
D O I
10.1139/P02-115
中图分类号
O4 [物理学];
学科分类号
0702 ;
摘要
The thermodynamic changes (DeltaH, DeltaS, and DeltaG) for the association of several small molecules (tetrahydrofuran (THF), ethylene oxide (EO), acetone) with water to form corresponding clathrate hydrates are calculated as a function of temperature from experimental information. For THF clathrate hydrate and EO clathrate hydrate at low temperatures, the clathrate is enthalpically stabilized with respect to the components. This is also the likely case for acetone clathrate hydrate. In all the three cases, above the melting points of the guest species, the clathrate increases in enthalpic stability, but entropic factors favour the separated components. Similar changes for THF clathrate hydrate and EO clathrate hydrate occur at the melting point of ice, eventually favouring the liquid components over the clathrate.
引用
收藏
页码:175 / 182
页数:8
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