Effect of synthesis method on selective adsorption of thiosulfate by calcined MgAl-layered double hydroxides

•Calcined MgAl-LDHs could separate S2O32- from mixed SCN− by selective adsorption.•The synthesis method of calcined MgAl-LDHs influenced their adsorption performance.•Calcined MgAl-LDH obtained using urea decomposition method presented the better adsorption selectivity for S2O32-.•Different adsorpti...

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Published inChemical engineering journal (Lausanne, Switzerland : 1996) Vol. 232; pp. 510 - 518
Main Authors Geng, Cuiyu, Xu, Tianhao, Li, Yaping, Chang, Zheng, Sun, Xiaoming, Lei, Xiaodong
Format Journal Article
LanguageEnglish
Published Elsevier B.V 01.10.2013
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Summary:•Calcined MgAl-LDHs could separate S2O32- from mixed SCN− by selective adsorption.•The synthesis method of calcined MgAl-LDHs influenced their adsorption performance.•Calcined MgAl-LDH obtained using urea decomposition method presented the better adsorption selectivity for S2O32-.•Different adsorption behaviors over the two calcined MgAl-LDH were studied. Calcined MgAl-layered double hydroxides (CLDH-U) derived from layered double hydroxide (LDH) precursors synthesized by urea decomposition, had the higher adsorption selectivity for thiosulfate (S2O32-) in aqueous solutions mixed with thiocyanate (SCN−) than the counterpart (CLDH-C) obtained by co-precipitation method. The adsorption rates for S2O32- over CLDH-U with diameter in 2μm and CLDH-C with diameter in 50nm were respectively about 98.00% and 94.80%, and those for SCN− were only about 0% and 6.84%. The results revealed that the selective adsorption was realized over these CLDH materials and the synthesis method influenced the adsorption behavior. The reason for the better selectivity over CLDH-U could be probably related to these mini sheets growing perpendicularly to the lamellate surface, which completely differed to the adsorption process over the small-sized counterpart. The different adsorption mechanisms of two CLDH materials were respectively proposed.
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ISSN:1385-8947
1873-3212
DOI:10.1016/j.cej.2013.08.010