化学
膦酸盐
双功能
铀
部分
萃取(化学)
硝酸
剥离(纤维)
配体(生物化学)
无机化学
磷酸
选择性
磷酸盐
核化学
分子
有机化学
材料科学
受体
催化作用
冶金
复合材料
生物化学
作者
A. Artese,Sandrine Dourdain,N. Felines,Guilhem Arrachart,N. Boubals,Philippe Guilbaud,Stéphane Pellet‐Rostaing
标识
DOI:10.1080/07366299.2020.1790527
摘要
Bifunctional amidophosphonate derivatives, already known as efficient ligands in uranium extraction from phosphoric media, have been evaluated and compared to the conventional tri-n-butyl phosphate (TBP) for uranium extraction from nitrate medium. The efficiency of U extraction and its selectivity towards competing elements such as Th, Zr, Mo, Fe, and V was evaluated with various ligand structures. It was found that extractant molecules containing a monosaponified phosphonate moiety instead of phosphonate moieties are less effective and selective. Furthermore, it was observed that the alkylation of the methylene bridge linking the two functional groups prevents the formation of precipitates during the uranium loading. Effects of acidity as well as ligand concentration were also investigated in order to estimate the loading capacity of the molecules. More detailed stoichiometry and transfer energy were further determined by the slope analysis method and a thermodynamic study. The possible uranium recovery from the organic phase has moreover been demonstrated thanks to stripping steps at low nitric acid concentration.
科研通智能强力驱动
Strongly Powered by AbleSci AI