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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.
Daojie Dong, George F. Vandegrift
Nuclear Science and Engineering | Volume 126 | Number 2 | June 1997 | Pages 213-223
Technical Paper | doi.org/10.13182/NSE97-A24474
Articles are hosted by Taylor and Francis Online.
The recent progress on the alkaline peroxide processing of low-enriched uranium targets for the production of 99Mo, a parent nuclide of the widely used medical isotope 99mTc, is reported. Kinetic studies were undertaken to investigate the decomposition of hydrogen peroxide in alkaline solution in contact with a uranium metal surface. It was found that the decomposition of hydrogen peroxide essentially follows the kinetic trend of uranium dissolution and can be classified into two regimes, depending on the hydroxide concentration. In the low-base regime (<0.2 M), both the hydrogen peroxide and hydroxide concentrations affect the rate of peroxide decomposition. In the high-base regime (>0.2 M), the rate of peroxide decomposition is independent of alkali concentration. When the acid/base equilibrium between H2O2 and O2H− is taken into account, the overall rate of hydrogen peroxide disappearance can be described as a 0.25th order reaction with respect to hydrogen peroxide concentration over NaOH concentrations ranging from 0.01 to 5 M. Empirical kinetics models are proposed and discussed.