Reactions of Atomic Thorium and Uranium Cations with SF 6 Studied by Guided Ion Beam Tandem Mass Spectrometry
The fundamental chemistry of the thorium and uranium fluorides continues to be an area of interest because of the use of thorium and uranium fluoride compounds in nuclear fuel systems. Here, we study the reaction of thorium cations with sulfur hexafluoride for the first time and revisit the reaction...
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Published in | The journal of physical chemistry. A, Molecules, spectroscopy, kinetics, environment, & general theory Vol. 126; no. 20; pp. 3239 - 3246 |
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Main Authors | , , |
Format | Journal Article |
Language | English |
Published |
United States
26.05.2022
|
Online Access | Get full text |
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Summary: | The fundamental chemistry of the thorium and uranium fluorides continues to be an area of interest because of the use of thorium and uranium fluoride compounds in nuclear fuel systems. Here, we study the reaction of thorium cations with sulfur hexafluoride for the first time and revisit the reaction of uranium cations with sulfur hexafluoride. By using guided ion beam tandem mass spectrometry, we explore the reaction pathways that become accessible well above thermal energies (
∼ 0.04 eV). Overall, we find that both Th
and U
react very efficiently with SF
, approaching the collision limit at both thermal and elevated energies. The primary products observed at low energies include Th
, UF
, and SF
, all of which are formed in barrierless, exothermic processes. SF
was also observed, although the pressure dependence of this channel reveals that SF
forms exothermically through secondary reactions, which the energy dependences suggest result from reactions between ThF
and UF
with SF
. At higher energies, both AnF
products are observed to decay to AnF
+ F
, and both SF
and SF
exhibit cross sections with endothermic features. For both systems, the rise in SF
can be attributed to a secondary collision between AnF
with SF
on the basis of the pressure dependence of the SF
channel at higher energies, and the rise in SF
appears to result from the decomposition of SF
to SF
+ F. |
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ISSN: | 1089-5639 1520-5215 |
DOI: | 10.1021/acs.jpca.2c02090 |