Abstract

The hydrolysis of uranium hexafluoride has been examined with infrared spectroscopy under three different reaction conditions. First, UF{sub 6} was codeposited with water in excess argon at 12 K. The FTIR spectra of UF{sub 6}/H{sub 2}O mixtures revealed several product absorptions due to the perturbed v{sub 1}, v{sub 2}, and v{sub 3} modes of H{sub 2}O as well as the v{sub 3} mode of UF{sub 6}. These new absorptions have been assigned to the anti-hydrogen-bonded 1:1 complex, UF{sub 6}-OH{sub 2}. Photolysis of this weak complex produced a doublet at 868.2 and 857.1 cm{sup -1}, which has been assigned to the UOF{sub 4}. Next, solid films of UF{sub 6}/H{sub 2}O mixtures were prepared at 12 K and slowly annealed at 242 K. The reaction profile of the UF{sub 6} hydrolysis from UF{sub 6} hydrolysis from UF{sub 6} (or UF{sub 6}-OH{sub 2}) to UOF{sub 4} to UO{sub 2}F{sub 2} was obtained. Finally, UF{sub 6} and H{sub 2}O were reacted at low pressures and ambient temperatures in a new IR gas cell. While no gaseous uranium oxyfluorides were detected, the final product distribution inside the gas cell did indicate that the fluorinated nickel surface served as a catalyst for the UF{sub 6} hydrolysis.more » 21 refs., 4 figs., 1 tab.« less

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.