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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.
Yasuki Kowata, Nobuo Fukumura
Nuclear Science and Engineering | Volume 115 | Number 3 | November 1993 | Pages 205-218
Technical Paper | doi.org/10.13182/NSE93-A24050
Articles are hosted by Taylor and Francis Online.
The influence of burnable gadolinia poison in fuel assemblies on coolant void reactivity for a pressure-tube-type boiling light-water-cooled heavy water reactor is investigated in critical experiments using the Deuterium Critical Assembly (DCA) and theoretical analyses by the WIMS-D4/ CITATION code system. The experimental and the calculated void reactivities agree within ±0.2 $., A number of gadolinia-poisoned fuel assemblies are dispersively loaded in the central region of the DCA core together with unpoisoned fuel assemblies. Each gadolinia-poisoned assembly is composed of three or four Gd2O3-poisoned UO2fuel rods as well as unpoisoned fuel rods. The gadolinia concentration is varied from 0.0 to 1.0 wt%., The void reactivity in the core becomes less negative with the addition of gadolinia but become saturated at a Gd2O3 concentration of ≈0.5 wt%. The void reactivity becomes much less negative with a higher loading ratio of the gadolinia-poisoned assemblies in the core and as the gadolinia-poisoned fuel rods are arranged in the outer layers of the assembly. When the fissile nuclide in the pellets of the unpoisoned fuel assembly is changed from uranium to plutonium, the incremental positive shift of the void reactivity can be reduced because of the increase in the 0.3-eV thermal resonance absorption of 239Pu and 241 Pu.