TY - JOUR
T1 - Fluorine gettering by activated charcoal in a radiation environment
AU - Felker, L. K.
AU - Toth, L. M.
PY - 1988/10/1
Y1 - 1988/10/1
N2 - Activated charcoal has been shown to be an effective gettering agent for the fluorine gas that is liberated in a radiation environment. Even though activated charcoal is a commonly used getter, little is known about the radiation stability of the fluorine-charcoal product. This work has shown that not only is the product stable in high gamma radiation fields, but also that radiation enhances the capacity of the charcoal for the fluorine. The most useful application of this work is with the Molten Salt Reactor Experiment (MSRE) fuel salt because the radioactive components (fission products and actinides) cause radiolytic damage to the solid LiF-BeF2-ZrF4-UF4 (64.5, 30.3, 5.0, 0.13 mol %, respectively) resulting in the liberation of fluorine gas. This work has also demonstrated that the maximum damage to the fuel salt by ~3 × 107 R/h gamma radiation is approximately 2%, at which point the the rate of recombination of fluorine with active metal sites within the salt lattice equals the rate of fluorine generation. The enhanced reactivity of the activated charcoal and radiation stability of the product ensures that the gettered fluorine will stay sequestered in the charcoal.
AB - Activated charcoal has been shown to be an effective gettering agent for the fluorine gas that is liberated in a radiation environment. Even though activated charcoal is a commonly used getter, little is known about the radiation stability of the fluorine-charcoal product. This work has shown that not only is the product stable in high gamma radiation fields, but also that radiation enhances the capacity of the charcoal for the fluorine. The most useful application of this work is with the Molten Salt Reactor Experiment (MSRE) fuel salt because the radioactive components (fission products and actinides) cause radiolytic damage to the solid LiF-BeF2-ZrF4-UF4 (64.5, 30.3, 5.0, 0.13 mol %, respectively) resulting in the liberation of fluorine gas. This work has also demonstrated that the maximum damage to the fuel salt by ~3 × 107 R/h gamma radiation is approximately 2%, at which point the the rate of recombination of fluorine with active metal sites within the salt lattice equals the rate of fluorine generation. The enhanced reactivity of the activated charcoal and radiation stability of the product ensures that the gettered fluorine will stay sequestered in the charcoal.
UR - http://www.scopus.com/inward/record.url?scp=0024091664&partnerID=8YFLogxK
U2 - 10.1080/01496398808075676
DO - 10.1080/01496398808075676
M3 - Article
AN - SCOPUS:0024091664
SN - 0149-6395
VL - 23
SP - 1959
EP - 1968
JO - Separation Science and Technology (Philadelphia)
JF - Separation Science and Technology (Philadelphia)
IS - 12-13
ER -