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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.
Edward T. Maas, Jr., John M. Longo
Nuclear Technology | Volume 47 | Number 3 | March 1980 | Pages 451-456
Technical Paper | Chemical Processing | doi.org/10.13182/NT80-A32399
Articles are hosted by Taylor and Francis Online.
While many materials have been suggested and employed as trapping agents for gaseous oxides of fission product ruthenium volatilized during nuclear fuels reprocessing, none that is known to form thermodynamically stable compounds with ruthenium has been utilized. We have employed alkaline earth metal compounds for this purpose because of their ability to form stable mixed metal oxide phases with ruthenium. Results of experiments in which RuO4 was volatilized from either a solid source (RuO2·xH2O) or from solution {[Ru(NO)(NO3)3] in HNO3} and passed through beds of alkaline earth metal carbonates and calcium oxide held at 600 to 750°C have demonstrated that compounds of formulation MRuO3 (M = calcium, strontium, barium) are formed. Under oxidizing conditions, these materials exist as stable ceramic phases, whereas under reducing conditions, they are transformed into intimate mixtures of the alkaline earth metal oxide and nonvolatile ruthenium metal.