alkaline earth chlorides
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2017 ◽  
Vol 250 ◽  
pp. 65-71 ◽  
Author(s):  
Faouzi Ayari ◽  
Rania Charrad ◽  
Esther Asedegbega–Nieto ◽  
Mourad Mhamdi ◽  
Gérard Delahay ◽  
...  


2011 ◽  
Vol 509 (13) ◽  
pp. 4445-4451 ◽  
Author(s):  
Aleksander Zych ◽  
Anke Leferink op Reinink ◽  
Koen van der Eerden ◽  
Celso de Mello Donegá ◽  
Andries Meijerink


Author(s):  
Ruth Weidemann ◽  
Gundula Jänsch-Kaiser ◽  
David H. Sharp




Author(s):  
Yung-Zun Cho ◽  
In-Tae Kim ◽  
Hee-Chul Yang ◽  
Hee-Chul Eun ◽  
Hwan-Seo Park ◽  
...  

Separation of some alkaline-earth chlorides (Sr, Ba) was investigated by using carbonate injection method in LiCl-KCl eutectic and LiCl molten salts. The effects of the injected molar ratio of carbonate ([K2 (or Li2)CO3/Sr (or Ba)Cl2]) and the temperature (450–750 °C) on the conversion ratio of the Sr or Ba carbonate were determined. In addition, the form of the Sr and Ba carbonate resulting from the carbonation reaction with carbonates was identified via XRD and SEM-EDS analysis. In these experiments, the carbonate injection method can remove Sr and Ba chlorides effectively over 99% in both LiCl-KCl eutectic and LiCl molten salt conditions. When Sr and Ba were co-presented in the eutectic molten salt, they were carbonated in a form of Ba0.5Sr0.3CO3. And when Sr was present in LiCl molten salt, it was carbonated in the form of SrCO3. Carbonation ratio increased with a decreasing temperature and it was more favorable in the case of a K2CO3 injection than that of Li2CO3. Based on this experiment, it is postulated that carbonate precipitation method has the potential for removing alkali-earth chlorides from LiCl-KCl eutectic and LiCl molten salts.



2006 ◽  
Vol 341 (1) ◽  
pp. 75-83 ◽  
Author(s):  
Yunlan Su ◽  
Limin Yang ◽  
Zheming Wang ◽  
Xianglin Jin ◽  
Shifu Weng ◽  
...  


2001 ◽  
Vol 703 ◽  
Author(s):  
V. A. Sadykov ◽  
T. G. Kuznetsova ◽  
V. P. Doronin ◽  
T. P. Sorokina ◽  
D. I. Kochubei ◽  
...  

ABSTRACTSAXS and EXAFS were applied to study genesis of polynuclear zirconium hydroxyspecies in pillaring solutions as dependent upon the zirconium concentration, addition of alkaline-earth chlorides and aging. After the montmorillonite clay pillaring, the structure of zirconium nanopillars was characterized by applying X-ray structural analysis, UV-Vis, FTIRS of adsorbed CO and nitrogen adsorption isotherms. Main pillaring species appear to be nanorods comprised of several Zr4 tetramers. Basic structural features of the tetramers are preserved in zirconia nanoparticles fixed between alumosilicate layers in pillared clays. In calcined samples, those nanoparticles contain only bridging hydroxyls and/or oxygen anions responsible for bonding within pillars and between pillars and clay sheets.



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