QUANTITATIVE STRUCTURAL-ANALYSIS OF MULLITE BY AL-27 NUCLEAR-MAGNETIC-RESONANCE SATELLITE TRANSITION SPECTROSCOPY

被引:26
作者
KUNATHFANDREI, G
REHAK, P
STEUERNAGEL, S
SCHNEIDER, H
JAGER, C
机构
[1] MAX PLANCK INST POLYMER RES,D-55021 MAINZ,GERMANY
[2] UNIV JENA,PATF,D-07743 JENA,GERMANY
[3] BRUKER ANALYT MESSTECH GMBH,D-76287 RHEINSTETTEN,GERMANY
[4] DEUTSCH FORSCH ANSTALT LUFT & RAUMFAHRT,INST WERKSTOFF FORSCH,D-51147 COLOGNE,GERMANY
关键词
AL-27 MAGIC-ANGLE SPINNING NUCLEAR MAGNETIC RESONANCE; SATELLITE TRANSITION SPECTROSCOPY; MINERALS; MULLITE; QUADRUPOLE COUPLING PARAMETERS; CHEMICAL SHIFT;
D O I
10.1016/0926-2040(94)90001-9
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
Al-27 Nuclear magnetic resonance (NMR) satellite transition spectroscopy has been used for the quantitative investigation of the microstructure of polycrystalline 2/1-type mullite (approximate to 76 wt.-% Al2O3 and 24 wt. % SiO2). Using this method the chemical shifts, quadrupole interaction parameters and relative amount of Al in the various coordination polyhedra have been obtained with high accuracy. The additional suppression of second-order quadrupolar broadening of the Al-27 magic-angle spinning (MAS) spinning sidebands of the inner satellite transitions allows three different AlO4 units to be detected. The three AlO4 resonances with isotropic chemical shifts at 68, 53 and 45 ppm are associated with AlO4 polyhedra in the tetrahedral double chains [AlO4(T)], the tetrahedra adjacent to the oxygen vacancies [AlO4(T*)] and the tetrahedra AlO4(T') linked by Oc* with AlO4(T*), respectively. Our NMR study of a polycrystalline sample supports the results of previous single-crystal studies of Angel et al. [Am. Mineral., 76 (1991) 332], especially the exclusion of silicon from the tetrahedral sites linked by Oc*.
引用
收藏
页码:241 / 248
页数:8
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