CHARACTERIZATION OF SODIUM-CATIONS IN DEHYDRATED ZEOLITE NAX BY NA-23NMR-SPECTROSCOPY

Citation
M. Feuerstein et al., CHARACTERIZATION OF SODIUM-CATIONS IN DEHYDRATED ZEOLITE NAX BY NA-23NMR-SPECTROSCOPY, Solid state nuclear magnetic resonance, 7(2), 1996, pp. 95-103
Citations number
22
Categorie Soggetti
Chemistry Physical","Physics, Atomic, Molecular & Chemical","Physics, Condensed Matter
ISSN journal
09262040
Volume
7
Issue
2
Year of publication
1996
Pages
95 - 103
Database
ISI
SICI code
0926-2040(1996)7:2<95:COSIDZ>2.0.ZU;2-5
Abstract
Na-23 MAS, 2D nutation MAS, and DOR NMR spectroscopy has been applied to characterise the location of sodium cations in dehydrated zeolite N aX (Si/Al = 1.23). The Na-23 MAS NMR spectra recorded at three differe nt magnetic field strengths were decomposed by computer simulation int o five lines, which were attributed to five crystallographically disti nct cation sites known from X-ray diffraction studies. The assignments of the lines follow from electric field gradient calculations at the Na-23 nuclei applying a simple point charge model based on crystal str ucture data. A weak Gaussian line at low field (delta(iso) = -6 ppm) i s assigned to sodium cations at site I, two broad quadrupole patterns at the high-field side of the spectra are attributed to site I' (delta (iso) = -19 ppm, QCC = 5.2 MHz, eta = 0) and site II cations (delta(is o) = -15 ppm, QCC = 4.6 MHz, eta = 0), and two quadrupolar lines domin ating the central region of the spectra originate from Na+ at two diff erent III' sites (delta(iso) = -13 and -29 ppm, QCC = 2.6 and 1.6 MHz, eta = 0.7 and 0.9, respectively). Na+ ions located on a second I' sit e could be identified from the DOR NMR spectra. The line assignment is further corroborated by the reasonable agreement of the site occupanc ies estimated from the line intensities with those determined by X-ray diffraction. In addition, sodium site populations of five dehydrated zeolites NaX and NaY with Si/Al ratios between 1.09 and 4.0 were deriv ed from the Na-23 MAS NMR spectra.