Highly efficient adsorptive extraction of uranium from wastewater by novel kaolin aerogel.

An environment-friendly, low-cost and efficient kaolin aerogel adsorbent (named as KLA) was synthesized via a freeze-drying-calcination method to solve the defect of low uranium removal rate for kaolin (KL). The removal rate of uranium on KLA reached 90.6 %, which was much higher than that of KL (69.2 %) (C0 = 10 mg L-1, t = 24 h, pH = 5.0, T = 298 K and m/V = 1.0 g L-1). The uranium removal behavior on KLA was satisfied with Pseudo-second-order and Langmuir model, which meant that the uranium ions were immobilized on the surface of KLA via chemical reaction. Meanwhile, high temperature was in favor of the removal of uranium on KLA, indicating that the removal process was a spontaneous endothermic reaction. Compared with KL, KLA also presented better cycle ability and its removal rate of uranium was up to 80.5 % after three cycles, which was still higher than that of KL at the first cycle (74.5 %). On basis of the results of SEM, XRD, FT-IR and XPS, it could be concluded that uranium ions were adsorbed by KLA via complexation. Hence, KLA could be regarded as a feasible candidate for the removal of uranium from aqueous solution.

Explorations on efficient extraction of uranium with porous coal fly ash aerogels.

In order to explore a suitable uranium adsorbent with the advantages of low-cost, recyclability and high efficiency, porous coal fly ash aerogels with different size of coal fly ash were synthesized. Among them, PCFAA-1250 (prepared with 1250 mesh coal fly ash (CFA)) showed better adsorption performance and the maximum adsorption efficiency even approached 96.5% (C0 = 10 mg L-1, m/V = 1.0 g L-1, T = 298 K, t = 24 h and pH = 3.0), which was higher than most of previous adsorbents. Langmuir and pseudo-second-order models were more likely to be used to determine the removal behavior of uranium on PCFAA, illustrating that the adsorption reaction was uniform chemisorption. Meanwhile, the adsorption process on PCFAA was spontaneous. Notably, the desorption efficiencies of all of PCFAA were more than 80% after five cycles, which suggested that PCFAA possessed good recyclability, especially PCFAA-1250. Besides, the adsorption mechanism was further revealed via XPS and the uranium ions were immobilized on the surface of adsorbents through complexation. Based on above conclusions, it could be concluded that PCFAA-1250 had the potential to be a candidate for the extraction of uranium from wastewater.

Highly enhanced adsorption performance to uranium(VI) by facile synthesized hydroxyapatite aerogel.

In order to protect environment and save uranium resources, it was necessary to find a highly efficient adsorbent for uranium recovery from wastewater. In this work, we used a freeze-drying-calcination method to synthesize HAP aerogel to effectively remove uranium. Compared with commercially available nano-hydroxyapatite, HAP aerogel presented better adsorption performance. This was because the as-prepared HAP aerogel presented continuous porous structure, which could provide more active sites for the adsorption to uranium. The uranium removal efficiency of HAP aerogel arrived 99.4% within 10 min and the maximum adsorption capacity was up to 2087.6 mg g-1 at pH = 4.0 and 298 K. In addition, the immobilization of uranium on HAP aerogel was chemisorption, which was probably due to adsorption, dissolution-precipitation and ions exchange. These results indicated that the as-prepared HAP aerogel could be widely used as a high efficiency and potential adsorbent for the treatment of uranium-containing wastewater in the future.