Incoherent inelastic neutron scattering studies of nanoconfined water in clinoptilolite and heulandite zeolites

被引:32
|
作者
Ockwig, Nathan W. [2 ]
Cygan, Randall T. [2 ]
Hartl, Monika A.
Daemen, Luke L.
Nenoff, Tina M. [1 ,3 ]
机构
[1] Los Alamos Natl Lab, Manuel Lujan Jr Neutron Scattering Ctr, LANSCE LC, Los Alamos, NM 87545 USA
[2] Sandia Natl Labs, Dept Geochem, Albuquerque, NM 87185 USA
[3] Sandia Natl Labs, Surface & Interface Sci Dept, Albuquerque, NM 87185 USA
来源
JOURNAL OF PHYSICAL CHEMISTRY C | 2008年 / 112卷 / 35期
基金
美国能源部;
关键词
D O I
10.1021/jp803770v
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
In a continued effort studying the role of water in ion exchange processes of zeolites, a synthetic series of alkali and alkaline earth metal cation variants (Na+, K+, Rb+, Mg2+, and Ca2+) of the hydrated clinoptilolite (Si/Al approximate to 5) and heulandite (Si/Al approximate to 3.5) aluminosilicate zeolites is examined by incoherent inelastic neutron scattering (IINS). The low-frequency librational modes of water reveal the impact of nanoconfinement and framework charge within these isostructural aluminosilicate structures. The experimental IINS spectra are correlated with power spectra derived through molecular dynamics simulations. The impact of ion-zeolite, ion-water, and water-zeolite interactions on the hindered rotations (librations) of water molecules is explored as a function of Si/Al substitution, cation identity, and subnanometer confinement. The results indicate that electrostatic charge on the overall framework has a stronger influence than charge density of a given ion in the channel and that these effects become more pronounced as the charge difference between ion and zeolite is increased.
引用
收藏
页码:13629 / 13634
页数:6
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