标题:The co-adsorption of Cu2+ and Zn2+ with adsorption sites surface-lattice reforming on calcined layered double hydroxides
作者:Xiao, Yuxin; Sun, Mingming; Zhang, Lin; Gao, Xue; Su, Jixin; Zhu, Hong
作者机构:[Xiao, Yuxin; Sun, Mingming; Zhang, Lin; Gao, Xue; Su, Jixin] Shandong Univ, Sch Environm Sci & Engn, Jinan 250100, Peoples R China.; [Zhu, Hong] Sh 更多
通讯作者:Su, Jixin
通讯作者地址:[Su, JX]Shandong Univ, Sch Environm Sci & Engn, Jinan 250100, Peoples R China.
来源:RSC ADVANCES
出版年:2015
卷:5
期:36
页码:28369-28378
DOI:10.1039/c5ra01745a
摘要:In this paper, nano-amorphous Mg/Al oxides-calcined layered double hydroxides (CLDHs) were employed to evaluate the adsorption capacity of Cu2+ or Zn2+ in wastewater and to investigate the adsorption mechanism. The results demonstrated that the maximal adsorption capacities of Cu2+ and Zn2+ were 422.08 mg g(-1) and 508.21 mg g(-1), respectively, whereas the initial Cu2+ or Zn2+ concentration in singleion solutions was 500 mg L-1. Certain competitive and inhibitory effects were observed during the Cu2+ and Zn2+ binary ions adsorption process. During the process, CLDHs were hydrated, and heavy metal ions were adsorbed rapidly onto the surface of CLDHs with crystalline phase inversion and formation of octahedral sheets with positive charges. Then, the sheets were stripped into the solution and the hydroxyls intercalated into the interlayer to make sheets combined together. Consequently, CLDHs recovered their hydrotalcite structure, which reflected the transition from surface adsorption to bulk phase. Thermodynamics study indicated that the adsorption isotherm was of the Langmuir-type. The kinetic model was of the pseudo-second-order-type. The regenerative adsorption experiments suggested that CLDHs could remove Cu2+ or Zn2+ with high efficiency after 4 repetitions. Both the high density bulk adsorption sites and the superior performance indicate a vast potential application prospect of the material.
收录类别:EI;SCOPUS;SCIE
WOS核心被引频次:5
Scopus被引频次:7
资源类型:期刊论文
原文链接:https://www.scopus.com/inward/record.uri?eid=2-s2.0-84961291941&doi=10.1039%2fc5ra01745a&partnerID=40&md5=4a354353303ee3d0cfd3f3e394359166
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