Raman spectroscopic studies of hydrogen clathrate hydrates

被引:91
作者
Strobel, Timothy A. [1 ]
Sloan, E. Dendy [1 ]
Koh, Carolyn A. [1 ]
机构
[1] Colorado Sch Mines, Dept Chem Engn, Ctr Hydrate Res, Golden, CO 80401 USA
关键词
deuterium; hydrogen neutral molecules; isotope effects; organic compounds; Raman spectra; red shift; rotational states; rotons; vibrational states; VIBRATIONAL FREQUENCY-SHIFT; SMALL DODECAHEDRAL CAGE; INFRA-RED SPECTROSCOPY; MOLECULAR-HYDROGEN; STORAGE; H-2; PRESSURE; ROTATION; CLUSTERS; TETRAHYDROFURAN;
D O I
10.1063/1.3046678
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
Raman spectroscopic measurements of simple hydrogen and tetrahydrofuran+hydrogen sII clathrate hydrates have been performed. Both the roton and vibron bands illuminate interesting quantum dynamics of enclathrated H-2 molecules. The complex vibron region of the Raman spectrum has been interpreted by observing the change in population of these bands with temperature, measuring the absolute H-2 content as a function of pressure, and with D-2 isotopic substitution. Quadruple occupancy of the large sII clathrate cavity shows the highest H-2 vibrational frequency, followed by triple and double occupancies. Singly occupied small cavities display the lowest vibrational frequency. The vibrational frequencies of H-2 within all cavity environments are redshifted from the free gas phase value. At 76 K, the progression from ortho- to para-H-2 occurs over a relatively slow time period (days). The rotational degeneracy of H-2 molecules within the clathrate cavities is lifted, observed directly in splitting of the para-H-2 roton band. Raman spectra from H-2 and D-2 hydrates suggest that the occupancy patterns between the two hydrates are analogous, increasing confidence that D-2 is a suitable substitute for H-2. The measurements suggest that Raman is an effective and convenient method to determine the relative occupancy of hydrogen molecules in different clathrate cavities.
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页数:10
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