Displacement of carbonates in Ca2UO2(CO3)3 by amidoxime-based ligands from free-energy simulationsElectronic supplementary information (ESI) available: Force field parameters for the inorganic components; AMBER input files for the organic ligands (AO−, HB−, and B2−). See DOI: 10.1039/c7dt03412a

• Main Authors: Li, Bo, Priest, Chad, Jiang, De-en
• Format: Journal Article
• Language: English
• Published: 30.01.2018
• ISSN: 1477-9226; 1477-9234
• DOI: 10.1039/c7dt03412a

Amidoxime-based ligands are effective in uranium extraction by displacing carbonates in Ca 2 UO 2 (CO 3 ) 3 , the dominant uranyl species in seawater. However, a detailed understanding of the displacement process has been lacking. Here we use classical molecular dynamics combined with umbrella sampling to map the complete displacement process and the free-energy profiles by the simple acetamidoximate (AO − ) and the more complex glutardiamidoximate (B 2− and HB − ) ligands. Interestingly, we find that the two Ca 2+ ions in Ca 2 UO 2 (CO 3 ) 3 can greatly facilitate the displacement of the first two carbonate groups. Displacing the third carbonate is however significantly more uphill than the first two. With the help of an additional Ca 2+ ion, the third carbonate displacement can be made less uphill. Comparing AO − and B 2− /HB − ligands, we find that the displacement by the latter is thermodynamically more favorable due to the chelate effect. Our free-energy simulations based on classical molecular dynamics simulations reveal key atomistic details and quantify the thermodynamic driving force during the carbonate displacement of Ca 2 UO 2 (CO 3 ) 3 by amidoxime-based ligands. These findings will be useful in understanding seawater uranium extraction by amidoxime-grafted polymeric sorbents. Classical molecular dynamics simulations coupled with umbrella sampling reveal the atomistic processes and free-energy profiles of the displacement of carbonate groups in the Ca 2 UO 2 (CO 3 ) 3 complex by amidoxime-based ligands in a 0.5 M NaCl solution.