沸石
化学
氨
核磁共振谱数据库
光谱学
吸附
核磁共振波谱
固态核磁共振
表征(材料科学)
水解
谱线
催化作用
无机化学
物理化学
材料科学
核磁共振
有机化学
纳米技术
物理
量子力学
天文
作者
Jian Jiao,Wei Wang,Bogdan Sulikowski,Jens Weitkamp,Michael Hunger
标识
DOI:10.1016/j.micromeso.2005.08.006
摘要
Solid-state NMR characterization of zeolite catalysts in the hydrated state is often accompanied by an uncontrolled hydrolysis of the framework. In the present work it is demonstrated that the limitations occurring for 29Si and 27Al MAS NMR spectroscopy of non-hydrated zeolites Y, such as strong decrease of resolution and significant line broadening, can be overcome by loading these materials with ammonia. In the 29Si MAS NMR spectra of non-hydrated and ammonia-loaded zeolites Y, no dehydration-induced high-field shift of Si(nAl) signals (n = 3, 2, 1) occurs, which is generally responsible for the loss of resolution in the spectra of non-hydrated materials. The 27Al MAS NMR spectra of the non-hydrated and ammonia-loaded zeolites Y consist exclusively of signals of the tetrahedrally coordinated framework aluminum atoms with spectroscopic parameters similar to those of framework aluminum atoms in hydrated samples. The framework nSi/nAl ratios of the non-hydrated zeolites Y obtained by both 29Si and 27Al MAS NMR spectroscopy upon ammonia-loading agree well with each other.
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