Volume 13 Issue 3
May  2023
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ZHAO J Y,LIU Y H,WANG Z M,et al.Influence mechanism of amide-based amphoteric molecules on uranium adsorption capacity of WS2[J].Journal of Environmental Engineering Technology,2023,13(3):1118-1126 doi: 10.12153/j.issn.1674-991X.20220498
Citation: ZHAO J Y,LIU Y H,WANG Z M,et al.Influence mechanism of amide-based amphoteric molecules on uranium adsorption capacity of WS2[J].Journal of Environmental Engineering Technology,2023,13(3):1118-1126 doi: 10.12153/j.issn.1674-991X.20220498

Influence mechanism of amide-based amphoteric molecules on uranium adsorption capacity of WS2

doi: 10.12153/j.issn.1674-991X.20220498
  • Received Date: 2022-05-20
  • The recovery of uranium from uranium-containing wastewater is mainly based on the complexation between the material and UO2 2+ in [UO2(H2O)5]2+, but the electric dipole moment of H2O has a significant weakening effect on the complexation. The amide-based amphoteric molecule N,N-dimethyl-9-decenyl amide (NADA) was used for hydrogen bonding with [UO2(H2O)5]2+ to form UO2[(H2O)xC12H23NO]n * (x<5, UO2-Coordination Compound was named UO2-CC) ,Inert tungsten disulfide (WS2) was selected as the adsorption material, and the adsorption capacities of UO2 2+ and UO2-CC were studied by static adsorption experiments (different pH, contact time, concentration and temperature). The kinetic fitting results showed that the adsorption reaction was a chemisorption process. After NADA reconstruction, the adsorption time of UO2 2+ was shortened from 240 min to 180 min, and the quasi-second-order kinetic adsorption constant was increased by 1.35 times. The results of the isothermal adsorption study showed that the complexation process of WS2 and UO2-CC conformed to the Langmuir adsorption isothermal model, and the addition of NADA made the adsorption change from spontaneous endothermic process to spontaneous exothermic process, and the order degree of the adsorption reaction process increased. After in situ reconstruction of [UO2(H2O)5]2+ by NADA, the equilibrium adsorption capacity of UO2 2+ by WS2 increased from 45.03 mg/g (WS2/UO2 2+ system) to 122.14 mg/g (WS2/UO2-CC system). Spectroscopic analysis by X-ray photoelectron spectroscopy was used to deeply study the adsorption mechanism of NADA on WS2 after in situ reconstruction of [UO2(H2O)5]2+ at the molecular level, and to reveal the contribution of various forces (electrostatic, hydrogen bond and U-S covalent bond) to adsorption, especially the hydrogen bond of NADA.

     

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