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Fast and Selective Removal of Aqueous Uranium by a K+-Activated Robust Zeolitic Sulfide with Wide pH Resistance.
Zhang, Bo; Sun, Hai-Yan; Li, Jun; Li, Lian-Zhi; Deng, Yan-Li; Liu, Shu-Hua; Feng, Mei-Ling; Huang, Xiao-Ying.
Afiliação
  • Zhang B; School of Chemistry and Chemical Engineering, Shandong Provincial Key Laboratory and Collaborative Innovation Center of Chemical Energy Storage & Novel Cell Technology , Liaocheng University , Liaocheng , Shandong 252059 , People's Republic of China.
  • Sun HY; State Key Laboratory of Structural Chemistry , Fujian Institute of Research on the Structure of Matter, Chinese Academy of Sciences , Fuzhou , Fujian 350002 , People's Republic of China.
  • Li J; State Key Laboratory of Structural Chemistry , Fujian Institute of Research on the Structure of Matter, Chinese Academy of Sciences , Fuzhou , Fujian 350002 , People's Republic of China.
  • Li LZ; School of Chemistry and Chemical Engineering, Shandong Provincial Key Laboratory and Collaborative Innovation Center of Chemical Energy Storage & Novel Cell Technology , Liaocheng University , Liaocheng , Shandong 252059 , People's Republic of China.
  • Deng YL; State Key Laboratory of Structural Chemistry , Fujian Institute of Research on the Structure of Matter, Chinese Academy of Sciences , Fuzhou , Fujian 350002 , People's Republic of China.
  • Liu SH; School of Chemistry and Chemical Engineering, Shandong Provincial Key Laboratory and Collaborative Innovation Center of Chemical Energy Storage & Novel Cell Technology , Liaocheng University , Liaocheng , Shandong 252059 , People's Republic of China.
  • Feng ML; School of Chemistry and Chemical Engineering, Shandong Provincial Key Laboratory and Collaborative Innovation Center of Chemical Energy Storage & Novel Cell Technology , Liaocheng University , Liaocheng , Shandong 252059 , People's Republic of China.
  • Huang XY; School of Chemistry and Chemical Engineering, Shandong Provincial Key Laboratory and Collaborative Innovation Center of Chemical Energy Storage & Novel Cell Technology , Liaocheng University , Liaocheng , Shandong 252059 , People's Republic of China.
Inorg Chem ; 58(17): 11622-11629, 2019 Sep 03.
Article em En | MEDLINE | ID: mdl-31411464
ABSTRACT
For the nuclear industry, uranium is not only an important strategic resource but also a serious global contaminant with radiotoxicity and high chemotoxicity. It is very important to efficiently capture uranium from complex aqueous solutions for further treatment and disposal of nuclear wastes. Herein, we first demonstrate the suitability of a three-dimensional (3D) water-stable K+-exchanged zeolitic sulfide, namely K@GaSnS-1, for the remediation of radioactive and toxic uranium by ion exchange. In comparison to the pristine compound GaSnS-1, the K+-activated porous sulfide K@GaSnS-1 exhibits faster [UO2]2+ ion uptake kinetics, following the pseudo-second-order adsorption model. Further studies indicate that K@GaSnS-1 shows high exchange capacity (qmU = 147.6 mg/g) and wide pH resistance (pH 2.75-10.87). In particular, it can efficiently capture [UO2]2+ ion even when excessive amounts of Na+, K+, Mg2+, and Ca2+ ions are present. The highest distribution coefficient value Kd, signifying the affinity and selectivity for [UO2]2+ ion, reaches as high as 1.24 × 104 mL/g. More importantly, the uranium in corresponding exchanged samples can be facilely and effectively eluted by a low-cost and eco-friendly method. These merits of K@GaSnS-1 make it promising for the effective and selective removal of uranium from complex contaminated water.

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Idioma: En Ano de publicação: 2019 Tipo de documento: Article

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Idioma: En Ano de publicação: 2019 Tipo de documento: Article