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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.
A. Gibello, F. V. Orestano, F. Pistella, E. Santandrea
Nuclear Science and Engineering | Volume 40 | Number 1 | April 1970 | Pages 51-72
Technical Paper | doi.org/10.13182/NSE70-A18879
Articles are hosted by Taylor and Francis Online.
Spectral indexes have been measured in homogeneous systems (solutions of europium and boron). The measured values have been compared with the results of spectra calculations and, independently, have been utilized for a correlation method devised to deduce the reaction rates which are undetectable directly. The reliability of the THERMOS code for spectra calculations in such systems has been shown. A satisfactory test of the correlation method has been performed. The adequacy of the cross-section sets available in the literature has been shown for the detectors 197Au, 63Cu, 55Mn, 176Lu, 239Pu, and 235U. The sets available for 151Eu and 175Lu are not satisfactory: new evaluations have been carried out by properly utilizing measurements reported in the literature and/or new measurements performed for this purpose in a known spectrum. When using the new sets, the agreement between calculated and experimental spectral indexes in the absorber solutions is significantly improved. When reliable cross sections are available for the detectors, the correlation method can be considered a powerful tool for the evaluation of an unknown reaction rate: for instance the 239Pu absorption rate in the solutions is evaluated by means of the measured activation rates without introducing uncertainties due to the correlation procedure itself.