Direct High-Resolution Transmission Electron Microscopic Measurement of Expandability of Mixed-Layer Illite/Smectite in Bentonite Rock

1990 ◽  
Vol 38 (4) ◽  
pp. 373-379 ◽  
Author(s):  
Jan Środoń
Clay Minerals ◽  
1985 ◽  
Vol 20 (2) ◽  
pp. 255-262 ◽  
Author(s):  
S. Mann ◽  
R. M. Cornell ◽  
U. Schwertmann

Aluminium-substituted goethites are found in many soils and can also be synthesised readily in the laboratory. In recent years, synthetic substituted goethites have been examined by various techniques including XRD, IR, TEM and dissolution kinetics (Thiel, 1963; Jonas & Solymar, 1970; Fey & Dixon, 1981; Fysh & Fredericks, 1983; Schulze & Schwertmann, 1984; Schwertmann, 1984). Transmission electron microscopy (TEM) studies have shown that as Al substitution rises above 10%, the goethite needles become shorter and also thicker in the a direction. Furthermore, crystals which at zero substitution consist of domains parallel to the c axis become less domainic with increasing Al substitution (Schulze & Schwertmann, 1984).


1998 ◽  
Vol 62 (1) ◽  
pp. 55-64 ◽  
Author(s):  
Wu Xiuling ◽  
Meng Dawei ◽  
Pan Zhaolu ◽  
Yang Guangming ◽  
Li Douxing

AbstractStructures of calcium-rare-earth (Ca-RE) fluorocarbonate minerals from southwest China have been investigated using selected area electron diffraction (SAED) and high-resolution transmission electron microscopy (HRTEM). They are described as combinations of layers of bastnäsite-(Ce), CeFCO3 (B layers), and synchysite-(Ce), CeFCO3·CaCO3 (S layers) (Donnay and Donnay, 1953). We report here the discovery of six new, regular, mixed-layer structures in parisite-(Ce) observed using SAED and HRTEM. The symmetry, cell parameters, chemical formulae and stacking of the structural unit layers, etc., were determined for each. The regular, mixed-layer structures are formed by stacking unit layers of bastnäsite-(Ce) and synchysite-(Ce) in varying proportions along the c axis. HRTEM shows that there are different distribution modes for the Ce-F ion layers, the CO3 ion groups between the Ce-F ion layers and the CO3 ion groups between the Ce-F and Ca ion layers. The minerals may be regarded as polymorphs with the same chemical composition and the same spacing of the unit layers, but different arrangements of ion layers in the structural unit layers and different stacking sequences of the structural unit layers.


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