Article ID | Journal | Published Year | Pages | File Type |
---|---|---|---|---|
4763105 | Chemical Engineering Journal | 2017 | 29 Pages |
Abstract
Efficient, irreversible capture of radioactive strontium and cesium from aqueous media remains a serious task for nuclear waste disposal and environmental protection. To address this task, an effective sorbent based on magnetic composites coated with the synthetic porous exchanger WO3 was prepared by a facile method and characterized in detail. XRD analysis indicated that the WO3 coating did not change the phase of the Fe3O4 core, and TEM imaging further showed that Fe3O4@WO3 particles were successfully obtained with nearly uniform size. A batch of experiments was carried out to investigate the efficiency of Fe3O4@WO3 in removing Sr2+ and Cs+ under various environmental conditions. Experimental results showed that Fe3O4@WO3 has higher adsorption capacity for Sr2+ and Cs+ in acidic aqueous solution in comparison to the previous literature. The theoretical maximum adsorption capacities of Fe3O4@WO3 for Sr2+ and Cs+ are 44.178 and 53.175 mg gâ1, respectively, as modeled by Langmuir isotherms. The adsorption process is fast and reaches equilibrium within 3 h, which is attributed to the good dispersion of WO3 on the surface of Fe3O4 and provided much more adsorption sites. Other than Ca2+ and K+, coexisting electrolyte ions had no significant competition effects on the removal of Sr2+ and Cs+ by Fe3O4@WO3. In addition, the Fe3O4@WO3 adsorbent remains stable in acidic solutions and may be repeatedly used 5 times without any noticeable loss in adsorption capacity; the used adsorbents can be easily separated from the aqueous solution using a magnetic method. The advantages of being nontoxic, highly stable, and resistant to acid, as well as having high adsorption capacity for Sr2+ and Cs+, indicate that Fe3O4@WO3 has significant potential for real radioactive wastewater treatment.
Related Topics
Physical Sciences and Engineering
Chemical Engineering
Chemical Engineering (General)
Authors
Wanjun Mu, Qianghong Yu, Xingliang Li, Hongyuan Wei, Yuan Jian,