Measurement of clathrate hydrates via Raman spectroscopy

被引:555
作者
Sum, AK [1 ]
Burruss, RC [1 ]
Sloan, ED [1 ]
机构
[1] COLORADO SCH MINES,CTR HYDRATE RES,DEPT CHEM ENGN,GOLDEN,CO 80401
来源
JOURNAL OF PHYSICAL CHEMISTRY B | 1997年 / 101卷 / 38期
关键词
D O I
10.1021/jp970768e
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 spectra of clathrate hydrate guest molecules are presented for three known structures (I (sI), II (sII), and H (sH)) in the following systems: CH4 (sI), CO2 (sI), C3H8 (sII), CH4 + CO2 (sI), CD4 + C3H8 (sII), CH4 + N-2 (sI), CH4 + THF-d(8) (sII), and CH4 + C7D14 (sH). Relative occupancy of CH4 in the large and small cavities of sI were determined by deconvoluting the nu(1) symmetric bands, resulting in hydration numbers of 6.04 +/- 0.03. The frequency of the nu(1) bands for CH4 in structures I, II, and H differ statistically, so that Raman spectroscopy is a potential tool to identify hydrate crystal structure. Hydrate guest compositions were also measured for two vapor compositions of the CH4 + CO2 system, and they compared favorably with predictions. The large cavities were measured to be almost fully occupied by CH4 and CO2, whereas only a small fraction of the small cavities are occupied by CH4. No CO2 was found in the small cavities. Hydration numbers from 7.27 to 7.45 were calculated for the mixed hydrate.
引用
收藏
页码:7371 / 7377
页数:7
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