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Going Nuclear: Notes from the officially unofficial book tour
I work in the analytical labs at one of Europe’s oldest and largest nuclear sites: Sellafield, in northwestern England. I spend my days at the fume hood front, pipette in one hand and radiation probe in the other (and dosimeter pinned to my chest, of course). Outside the lab, I have a second job: I moonlight as a writer and public speaker. My new popular science book—Going Nuclear: How the Atom Will Save the World—came out last summer, and it feels like my life has been running at full power ever since.
S. Sunder
Nuclear Technology | Volume 144 | Number 2 | November 2003 | Pages 259-273
Technical Paper | Materials for Nuclear Systems | doi.org/10.13182/NT03-A3443
Articles are hosted by Taylor and Francis Online.
The relationship between molybdenum oxidation state and iodine volatility in nuclear fuel was investigated using high-temperature Knudsen cell-mass spectroscopy. It was observed that the ratio of the intensities of molecular iodine ions I2+ and CsI+ in the Knudsen cell-mass spectroscopic experiments can be used to investigate the iodine volatility in fuel under different conditions. The experiments show that the iodine volatility is similar in systems consisting of CsI alone, CsI/UO2, and CsI/UO2/MoOx (with molybdenum in oxidation states 0, 2, and 4). The iodine volatility is much higher, however, in CsI/UO2/MoO3 systems (with molybdenum in oxidation state = 6). The iodine volatility in the fuel increases significantly if oxidation of the molybdenum goes to the MoO3 stage. The increase in the iodine volatility is caused by the formation of elemental iodine from cesium iodide. It is concluded from these measurements that the oxidation of the fuel to the UO2.2 will substantially increase the volatilization of fission product iodine. An analysis of the literature data suggests that the enhanced iodine volatilization process may be initiated when the fuel is oxidized to UO2.02.