Synthesis of enhanced phosphonic functional groups mesoporous silica for uranium selective adsorption from aqueous solutions

被引:64
作者
Sarafraz, H. [1 ]
Minuchehr, A. [1 ]
Alahyarizadeh, Gh. [1 ]
Rahimi, Z. [1 ]
机构
[1] Shahid Beheshti Univ, GC, Engn Dept, POB 1983969411, Tehran, Iran
关键词
SOL-GEL; SURFACE MODIFICATION; HIGH-PERFORMANCE; GRAPHENE OXIDE; URANYL IONS; REMOVAL; U(VI); EXTRACTION; SORPTION; METALS;
D O I
10.1038/s41598-017-11993-5
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
Enhanced phosphonic functional group (PFG)-based mesoporous silicas (MSs) were synthesized by hydrothermal method for uranium [U(VI)] selective adsorption from aqueous solutions. Considering that PFGs are directly related to U(VI) adsorption, the main idea of this research was to synthesize enhanced PFG-MSs and consequently enhance U(VI) adsorption. We synthesized two kinds of MSs based on acetic and phosphoric acids at weakly acidic pH, which allows high-loading phosphonic functionality. The main sodium and phosphonic functionality sources were sodium metasilicate and diethylphosphatoethyltriethoxysilane (DPTS). Adsorption experiment results exhibit enhanced U(VI) adsorption capacity from 55.75 mg/g to 207.6 mg/g for acetic and phosphoric acids, respectively. This finding was due to the enhancement of PFGs by phosphoric acids. The highest adsorption selectivity was 79.82% for U(VI) among the six different elements, including Pb, As, Cu, Mo, Ni, and K. Structural characterization of the samples was performed by Fourier transform infrared, X-ray diffraction, scanning electron microscopy, energy-dispersive X-ray spectroscopy, and Brunauer-Emmett-Teller analysis methods. Element concentrations were measured by inductively coupled plasma optical emission spectrometry. Several parameters affecting adsorption capacity, including pH, contact time, initial U(VI) concentration and solution volume, and adsorbent concentration, were also investigated.
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页数:12
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