Clathrate hydrates with hydrogen-bonding guests

被引:143
|
作者
Buch, Victoria [2 ]
Devlin, J. Paul [1 ]
Monreal, I. Abrrey [1 ]
Jagoda-Cwiklik, Barbara [2 ]
Uras-Aytemiz, Nevin [3 ]
Cwiklik, Lukasz [2 ]
机构
[1] Oklahoma State Univ, Dept Chem, Stillwater, OK 74078 USA
[2] Hebrew Univ Jerusalem, Fritz Haber Inst Mol Dynam, IL-91904 Jerusalem, Israel
[3] Suleyman Demirel Univ, Dept Chem, TR-32260 Isparta, Turkey
基金
美国国家科学基金会;
关键词
HETEROGENEOUS CRYSTAL-GROWTH; ICE PARTICLE CONVERSION; FT-IR SPECTRA; METHANE HYDRATE; CARBON-DIOXIDE; MONTE-CARLO; VIBRATIONAL FREQUENCIES; ORIENTATIONAL DEFECTS; MOLECULAR-DYNAMICS; WANNIER FUNCTIONS;
D O I
10.1039/b911600c
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
Clathrate hydrates (CHs) are inclusion compounds in which "tetrahedrally" bonded H2O forms a crystalline host lattice composed of a periodic array of cages. The structure is stabilized by guest particles which occupy the cages and interact with cage walls via van der Waals interactions. A host of atoms or small molecules can act as guests; here the focus is on guests that are capable of strong to intermediate H-bonding to water (small ethers, H2S, etc.) but nevertheless "choose" this hydrate crystal form in which H-bonding is absent from the equilibrium crystal structure. These CHs can form by exposure of ice to guest molecules at temperatures as low as 100-150 K, at the (low) guest saturation pressure. This is in contrast to the "normal" CHs whose formation typically requires temperatures well above 200 K and at least moderate pressures. The experimental part of this study addresses formation kinetics of CHs with H-bonding guests, as well as transformation kinetics between different CH forms, studied by CH infrared spectroscopy. The accompanying computational study suggests that the unique properties of this family of CHs are due to exceptional richness of the host lattice in point defects, caused by defect stabilization by H-bonding of water to the guests.
引用
收藏
页码:10245 / 10265
页数:21
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