Abstract

The objective of this study was the development and optimization of a method for the liquid–liquid extraction and recovery of Uranium (VI) traces (0.10mg/L). A comparison was made of three different extracting agents at 0.10mol/L: tri-n-butyl phosphate, methyltrioctylammonium chloride, and bis(2-ethylhexyl) phosphoric acid. As the optimized chemical conditions of the liquid–liquid systems are very important for the future applications for the extraction, recovery and pre-concentration of Uranium (VI) traces, whether in bulk liquid membranes or in supported liquid membranes systems, a response surface methodology was adopted. A Doehlert design is used to obtain a quadratic function relationship between the percentage of recovery of uranyl ion and the amount of bis(2-ethylhexyl) phosphoric acid in kerosene, as extracting agent (0.001–0.050mol/L) and that of phosphoric (0.192–0.718mol/L) and citric (0.206–0.698mol/L) acids, mixed as recovery agents. From the results, the most important effects on the recovery are the concentration of bis(2-ethylhexyl) phosphoric acid in the organic phase and the concentration of phosphoric acid in the stripping solution, while the concentration of citric acid only favors the extraction of Uranium (VI) when the other compounds are at opposite levels of concentration. From the mathematical model, optimal conditions for the back-extraction of Uranium (VI) were found with predicted recoveries of 99%, which were later corroborated experimentally.

Full Text
Paper version not known

Talk to us

Join us for a 30 min session where you can share your feedback and ask us any queries you have

Schedule a call

Disclaimer: All third-party content on this website/platform is and will remain the property of their respective owners and is provided on "as is" basis without any warranties, express or implied. Use of third-party content does not indicate any affiliation, sponsorship with or endorsement by them. Any references to third-party content is to identify the corresponding services and shall be considered fair use under The CopyrightLaw.