A novel U(vi)-imprinted graphitic carbon nitride composite for the selective and efficient removal of U(vi) from simulated seawater. Issue 9 (27th July 2018)

• Record Type: Journal Article
• Authors: Hao, Xuan; Chen, Rongrong; Liu, Qi; Liu, Jingyuan; Zhang, Hongsen; Yu, Jing; Li, Zhanshuang; Wang, Jun
• Is Part Of: Inorganic chemistry frontiers. Volume 5:Issue 9(2018)
• Page Start: 2218
• Page End: 2226
• Publication Date: 2018-07-27
• Subjects: Chemistry, Inorganic -- Periodicals; 546.05
• DOI: 10.1039/c8qi00522b
• Languages: English
• ISSNs: 2052-1553

Abstract

Abstract : A high selectivity U(vi )-imprinted g-C3 N4 /β-CD sorbent was synthesized and used for selective removal of U(vi ). The interaction mechanism is mainly surface complexation and electrostatic attraction. Abstract : Extracting uranium(vi ) from seawater for future long-term development of nuclear energy in the world is an urgent issue. However, there are still enormous challenges to selectively extract U(vi ) from seawater. In this paper, a high selectivity surface U(vi )-imprinted graphitic carbon nitride/β-cyclodextrin composite sorbent was synthesized through a cross-linking method with U(vi ) ions, β-cyclodextrin and epichlorohydrin as the template ion, the functional ligand and the cross-linking agent, respectively. The prepared ion-imprinted β-cyclodextrin modified graphitic carbon nitride polymer (IIP-g-C3 N4 /β-CD) was used for selective extraction of U(vi ) from aqueous solution. Effects of different conditions were examined such as solution pH, oscillation time, temperature, etc . The results suggested that the IIP-g-C3 N4 /β-CD exhibits wonderful adsorption capacity and outstanding selectivity for U(vi ) extraction at the ppm level compared to the nonimprinted material. The adsorption process closely correlates with the Langmuir adsorption isotherm model. In addition, the calculated maximum adsorption capacity was 859.66 mg g −1 at 25 °C, which confirmed that the adsorption process is a monolayer chemisorption process. Accordingly, the IIP-g-C3 N4 /β-CD showed excellent selective adsorption of U(vi ) and cycling stability after five adsorption–desorption cycles with little adsorption capacity loss. Moreover, IIP-g-C3 N4 /β-CD exhibited outstanding U(vi ) adsorption efficiency for simulated seawater indicating that IIP-g-C3 N4 /β-CD can be used as a potential sorbent for the efficient selective adsorption of U(vi ) from simulated seawater.