Advertisement

Preparation of a macroporous silica–pyridine multidentate material and its adsorption behavior for some typical elements

Authors

  • Anyun Zhang,

    Corresponding author
    1. Dept. of Chemical and Biochemical Engineering, Zhejiang University, Hangzhou 310027, P.R. China
    • Dept. of Chemical and Biochemical Engineering, Zhejiang University, Hangzhou 310027, P.R. China
    Search for more papers by this author
  • Wenjing Xue,

    1. Dept. of Chemical and Biochemical Engineering, Zhejiang University, Hangzhou 310027, P.R. China
    Search for more papers by this author
  • Zhifang Chai

    1. Dept. of Chemical and Biochemical Engineering, Zhejiang University, Hangzhou 310027, P.R. China
    2. Laboratory of Nuclear Analytical Techniques, Institute of High Energy Physics, Chinese Academy of Sciences, Beijing 100049, P.R. China
    Search for more papers by this author

Abstract

A new macroporous silica-based-polymer (SiO2-P) soft ligand composite material, 2,6-bis(5,6-di(iso-butyl)-1,2,4-triazine-3-yl)pyridine (BDIBTP/SiO2-P), was synthesized by impregnation and immobilization of BDIBTP and 1-octanol molecules into the pores of the SiO2-P particles. The impact of some typical alkali metal and alkaline earths Cs(I), Na(I), K(I), Rb(I), Sr(II), and Ba(II) containing in highly active liquid waste (HLW) on the adsorption of Pd(II) onto BDIBTP/SiO2-P was studied. It was performed by examining the effects of contact time and the HNO3 concentration in the range of 0.3–7.0 M. BDIBTP/SiO2-P showed strong adsorption ability and high selectivity for Pd(II) over all the tested metals. The chromatographic partitioning of Pd(II) from a simulated HLW solution was conducted by BDIBTP/SiO2-P packed column. Pd(II) was effectively eluted with 0.2 M thiourea–0.1 M HNO3. The others showed no adverse impact on separation of Pd(II). The results are beneficial to partitioning of minor actinides and Pd(II) together from HLW by BDIBTP/SiO2-P in the MPS process developed. © 2012 American Institute of Chemical Engineers AIChE J, 2012

Ancillary