CHARACTERIZATION OF SODIUM-CATIONS IN ZEOLITE OMEGA BY SOLID-STATE NA-23 NMR-SPECTROSCOPY

被引:4
|
作者
DENG, F
DU, Y
YE, C
WANG, K
CHEN, T
DING, D
WANG, J
LI, H
机构
[1] CHINESE ACAD SCI,WUHAN INST PHYS,NUCL MAGNET RESONANCE & MOLEC PHYS LAB,POB 71010,WUHAN 430071,PEOPLES R CHINA
[2] NANKAI UNIV,DEPT CHEM,TIANJIN,PEOPLES R CHINA
关键词
D O I
10.1007/BF03162643
中图分类号
O64 [物理化学(理论化学)、化学物理学]; O56 [分子物理学、原子物理学];
学科分类号
070203 ; 070304 ; 081704 ; 1406 ;
摘要
Sodium cations localized at crystallographically distinct cation sites in the hydrated zeolite omega were characterized by various solid-state Na-23 NMR techniques, such as Na-23 MAS, H-1-Na-23 CP/MAS, Na-23 quadrupolar nutation and variable temperature NMR spectroscopy. In the Na-23 NMR spectrum of zeolite omega two signals were identified, a low-field Gaussian line at ca. -3 ppm (its quadrupole coupling constant was estimated approximately on the order of magnitude of 0.2 MHz) and a high-field quadrupole pattern with an isotropic chemical shift of -8 ppm and a quadrupole coupling constant of 2.3 MHz. The former signal is attributed to sodium cations in the 12-ring channels and the latter one to sodium cations in gmelinite cages of zeolite omega. The variable temperature NMR experiments reveal the interactions between the sodium cation and the adsorbed water molecules in zeolite omega. The sodium cations in the 12-ring channels are highly hydrated and so mobile as to average the H-1-Na-23 dipole interaction. Hence, these sodium cations give no contribution to the H-1-Na-23 cross polarization process. By contrast, the sodium cations in the gmelinite cages are less hydrated and more rigid. They are closely bonded not only to the adsorbed water molecules but also to the lattice oxygen of the gmelinite cages, which leads to an effective H-1-Na-23 polarization transfer.
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页码:537 / 547
页数:11
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