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RP3C Community of Practice’s fifth anniversary
In February, the Community of Practice (CoP) webinar series, hosted by the American Nuclear Society Standards Board’s Risk-informed, Performance-based Principles and Policies Committee (RP3C), celebrated its fifth anniversary. Like so many online events, these CoPs brought people together at a time when interacting with others became challenging in early 2020. Since the kickoff CoP, which highlighted the impact that systems engineering has on the design of NuScale’s small modular reactor, the last Friday of most months has featured a new speaker leading a discussion on the use of risk-informed, performance-based (RIPB) thinking in the nuclear industry. Providing a venue to convene for people within ANS and those who found their way online by another route, CoPs are an opportunity for the community to receive answers to their burning questions about the subject at hand. With 50–100 active online participants most months, the conversation is always lively, and knowledge flows freely.
Sridhar Komarneni, Rustum Roy, Della M. Roy
Nuclear Technology | Volume 62 | Number 1 | July 1983 | Pages 71-74
Technical Paper | Radioactive Waste Management | doi.org/10.13182/NT83-A33233
Articles are hosted by Taylor and Francis Online.
The SrMoO4 compound, a host for strontium in tailored nuclear waste ceramics, is highly stable in deionized water, NaCl, KCl, and the acidic MgCl2under hydrothermal conditions of 100, 200 and 300°C as indicated by the fact that <0.5% strontium was released under these conditions. In Na2SO4solution, SrMoO4 is somewhat reactive, as indicated by the release of ≈2 and 6% of the original strontium and molybdenum inventories, respectively, into solution at 200 and 300°C. More molybdenum than strontium was detected in solution because of the crystallization of celestite, SrSO4. Thus, anions such as SO4 influence the reactivity of SrMoO4. The SrMoO4 phase was found to be least stable in CaCl2 solution as indicated by the release of 93.5, 96.1, and100% of the strontium from the initial SrMoO4at 100, 200, and 300°C, respectively. However, only 0.02% of the original inventory of molybdenum in SrMoO4 was detected in solution. The removal of molybdenum from solutions was due to the formation of CaMoO4 powellite as revealed by x-ray diffraction. Thus, CaMoO4 is more stable than SrMoO4under these hydrothermal conditions. These results show that SrMoO4 is stable in Na+, K+, and Mg2+ solutions but not in Ca2+-containing solutions