In Situ X-ray and Neutron Diffraction of the Rare-Earth Phosphate Proton Conductors Sr/Ca-Doped LaPO4 at Elevated Temperatures

2016 ◽  
Vol 28 (20) ◽  
pp. 7232-7240 ◽  
Author(s):  
A. al-Wahish ◽  
U. al-Binni ◽  
C. A. Bridges ◽  
S. Tang ◽  
Z. Bi ◽  
...  
2005 ◽  
Vol 351 (40-42) ◽  
pp. 3179-3190 ◽  
Author(s):  
Uwe Hoppe ◽  
Richard K. Brow ◽  
Dora Ilieva ◽  
Pal Jóvári ◽  
Alex C. Hannon

2011 ◽  
Vol 509 (14) ◽  
pp. 4707-4713 ◽  
Author(s):  
Min Yang ◽  
Kuo Li ◽  
Jie Su ◽  
Q. Huang ◽  
Wei Bao ◽  
...  

2007 ◽  
Vol 19 (5) ◽  
pp. 056002 ◽  
Author(s):  
Jacqueline M Cole ◽  
Adrian C Wright ◽  
Robert J Newport ◽  
Roger N Sinclair ◽  
Henry E Fischer ◽  
...  

Minerals ◽  
2021 ◽  
Vol 11 (3) ◽  
pp. 236
Author(s):  
Shenghua Yin ◽  
Xun Chen ◽  
Rongfu Yan ◽  
Leiming Wang

As an environmentally compliant hydrometallurgical process, in situ leaching is extensively used by the mining industry to recover rare earth from weathered crust elution-deposited rare earth ore. In the in situ leaching system, the pore structure plays a dominant role in the permeability of the rare earth orebody and is one of the most important factors that influence the leaching performance. To study the pore structure characteristics of the rare earth ore, an undisturbed ore sample was scanned using X-ray micro-computed tomography. Based on the image processing techniques, visualization of the pore structure was realized and several parameters of 2D and 3D pore structures, such as porosity, pore volume, length, width, aspect ratio, and orientation, were obtained and statistically analyzed. The ball-and-stick model of large pore clusters was built by the maximal ball algorithm, and some of their detailed characteristics were obtained. The results indicate that the pore structure of weathered crust elution-deposited rare earth ore exhibits a multi-scale and strong heterogeneity characteristic. The distribution characteristics of pores between the vertical direction and the horizontal direction are obviously different. The small pores are more prevalent in number, but they make only a small contribution to the total pore volume. In addition, the orientation of the pores is anisotropic in both vertical and horizontal directions. Furthermore, the ball-and-stick model reveals that large pore clusters are composed of several interconnected void spaces, and most of them are small and irregular.


2020 ◽  
Vol 0 (0) ◽  
Author(s):  
Michael Zoller ◽  
Hubert Huppertz

AbstractThe rare earth oxoborates REB5O8(OH)2 (RE = Ho, Er, Tm) were synthesized in a Walker-type multianvil apparatus at a pressure of 2.5 GPa and a temperature of 673 K. Single-crystal X-ray diffraction data provided the basis for the structure solution and refinement. The compounds crystallize in the monoclinic space group C2 (no. 5) and are composed of a layer-like structure containing dreier and sechser rings of corner sharing [BO4]5− tetrahedra. The rare earth metal cations are coordinated between two adjacent sechser rings. Further characterization was performed utilizing IR spectroscopy.


2021 ◽  
Vol 92 (3) ◽  
pp. 033704
Author(s):  
Rongqi Zhu ◽  
Zhaoliang Qu ◽  
Shuo Yang ◽  
Daining Fang
Keyword(s):  

2013 ◽  
Vol 68 (5-6) ◽  
pp. 625-634 ◽  
Author(s):  
Bastian Reker ◽  
Samir F. Matar ◽  
Ute Ch. Rodewald ◽  
Rolf-Dieter Hoffmann ◽  
Rainer Pöttgen

Small single crystals of the Sm5Ge4-type (space group Pnma) germanides RE2Nb3Ge4 (RE = Sc, Y, Gd-Er, Lu) and Sc2Ta3Ge4 were synthesized by arc-melting of the respective elements. The samples were characterized by powder and single-crystal X-ray diffraction. In all structures, except for Sc2.04Nb2.96Ge4 and Sc2.19Ta2.81Ge4, the rare earth and niobium atoms show full ordering on the three crystallographically independent samarium sites of the Sm5Ge4 type. Two sites with coordination number 6 are occupied by niobium, while the slightly larger site with coordination number 7 is filled with the rare earth element. Small homogeneity ranges with RE=Nb and RE=Ta mixing can be expected for all compounds. The ordered substitution of two rare earth sites by niobium or tantalum has drastic effects on the coordination number and chemical bonding. This was studied for the pair Y5Ge4/Y2Nb3Ge4. Electronic structure calculations show larger charge transfer from yttrium to germanium for Y5Ge4, contrary to Y2Nb3Ge4 which shows stronger covalent bonding due to the presence of Nb replacing Y at two sites


2003 ◽  
Vol 798 ◽  
Author(s):  
V. Katchkanov ◽  
J. F. W. Mosselmans ◽  
S. Dalmasso ◽  
K. P. O'Donnell ◽  
R. W. Martin ◽  
...  

ABSTRACTThe local structure around Er and Eu atoms introduced into GaN epilayers was studied by means of Extended X-ray Absorption Fine Structure above the appropriate rare-earth X-ray absorption edge. The samples were doped in situ during growth by Molecular Beam Epitaxy. The formation of ErN clusters was found in samples with high average Er concentrations of 32±6% and 12.4±0.8%, estimated by Wavelength Dispersive X-ray analysis. When the average Er concentration is decreased to 6.0±0.2%, 1.6±0.2% and 0.17±0.02%, Er is found in localised clusters of ErGaN phase with high local Er content. Similar behaviour is observed for Eu-doped samples. For an average Eu concentration of 30.5±0.5% clusters of pure EuN occur. Decreasing the Eu concentration to 10.4±0.5% leads to EuGaN clusters with high local Eu content. However, for a sample with an Eu concentration of 14.2±0.5% clustering of Eu was not observed.


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