Development of the chromatographic partitioning of cesium and strontium utilizing two macroporous silica-based calix[4]arene-crown and amide impregnated polymeric composites: PREC partitioning process

To partition effectively Cs(I) and Sr(II), two harmful heat emitting nuclides, from a highly active liquid waste by extraction chromatography, two kinds of macroporous silica-based polymeric materials, Calix[4]arene-R14/SiO2-P and TODGA/SiO2-P, were synthesized. Two chelating agents, 1,3-[(2.4-diethyl-heptylethoxy)oxyl-2,4-crown-6-calix[4]arene (Calix[4]arene-R14), an excellent supramolecular compound having molecular recognition ability for Cs(I), and N, N, N',N'-tetraoctyl-3-oxapentane-1,5-diamide (TODGA) were impregnated and immobilized into the pores of SiO2-P particles support by a vacuum sucking technique. The loading and elution of I I typical simulated fission and non-fission products from 4.0M or 2.0M HNO3 were performed at 298K. It was found that in the first column packed with the Calix[4]arene-R14/SiO2-P, all of the simulated elements were separated effectively into two groups: (1) Na(I), K(I), Sr(II), Fe(Ill), Ba(II), Ru(III), Pd(II), Zr(IV), and Mo(VI) (noted as Sr-group) (2) Cs(I)-Rb(I) (Cs-group) by eluting with 4.0M HNO3 and distilled water, respectively. The harmful element Cs(I) flowed into the second group along with Rb(l) because of their close sorption and elution properties towards Calix[4]arene-R14/SiO2-P while Sr(II) showed no sorption and flowed into Sr-containing group. In the second column packed with TODGA/SiO2-P, the Sr-group was separated into (1) Ba(11), Ru(III), Na(I), K(I), Fe(III), and Mo(VI) (non-sorption group); (2) Sr(II); (3) Pd(II); and (4) Zr(IV) by eluting with 2.0M HNO3, 0-01 M HNO3, 0.05 M DTPA-pH 2.5, and 0.5 M H2C2O4, respectively. Sr(II) adsorbed towards TODGA/SiO2-P flowed into the second group and showed the excellent separation efficiency from others. Based on the elution behavior of the tested elements, an advanced PREC (Partitioning and Recovery of two heat generators from an acidic HLW (high activity liquid waste) by Extraction Chromatography) process was proposed. (c) 2007 Elsevier B.V. All rights reserved.