2006年
Local structure of xenon adsorbed in the nanospaces of zeolites as studied by high-pressure Xe-129 NMR
PHYSICAL CHEMISTRY CHEMICAL PHYSICS
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- 巻
- 8
- 号
- 33
- 開始ページ
- 3857
- 終了ページ
- 3866
- 記述言語
- 英語
- 掲載種別
- DOI
- 10.1039/b604633a
- 出版者・発行元
- ROYAL SOC CHEMISTRY
Pressure (0-10 MPa) and local density dependence of Xe-129 NMR chemical shift of xenon in various microporous materials was investigated using an in situ high-pressure probe. The density dependence of the chemical shift was analyzed using virial expansion of the chemical shift by xenon density. Results indicate that the second virial coefficient depends on the pore size and shape, and that the void space affects xenon-xenon interaction in both microporous and mesoporous materials. Furthermore, to interpret the magnitude of the virial coefficient in terms of the local structure of the adsorbed xenon, we analyzed the local structure of adsorbed xenon in molecular sieve 5A using Xe-n clusters, thereby allowing description of the density dependence of the chemical shift. We also demonstrated the cluster model's validity by applying it to molecular sieves 13X and ZSM-5. The latter showed that the adsorbed xenon exists as a xenon monomer up to the filling of about 0.6 in micropores. Larger xenon clusters up to n = 4 have been grown with increasing filling of xenon. According to analyses using the Xen cluster model, the second virial coefficient is related closely with the xenon cluster size, which contributes greatly to the chemical shift in the low loading region.
- リンク情報
- ID情報
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- DOI : 10.1039/b604633a
- ISSN : 1463-9076
- Web of Science ID : WOS:000239937900014