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NRC looks to leverage previous approvals for large LWRs
During this time of resurging interest in nuclear power, many conversations have centered on one fundamental problem: Electricity is needed now, but nuclear projects (in recent decades) have taken many years to get permitted and built.
In the past few years, a bevy of new strategies have been pursued to fix this problem. Workforce programs that seek to laterally transition skilled people from other industries, plans to reuse the transmission infrastructure at shuttered coal sites, efforts to restart plants like Palisades or Duane Arnold, new reactor designs that build on the legacy of research done in the early days of atomic power—all of these plans share a common throughline: leveraging work already done instead of starting over from square one to get new plants designed and built.
Mélany Gouëllo, Jouni Hokkinen, Teemu Kärkelä, Ari Auvinen
Nuclear Technology | Volume 203 | Number 1 | July 2018 | Pages 66-84
Technical Paper | doi.org/10.1080/00295450.2018.1429111
Articles are hosted by Taylor and Francis Online.
This work is a contribution toward understanding the chemical reactions on the primary circuit surfaces involving gaseous iodine release during a severe nuclear reactor accident. Cesium iodide was used as a nonradioactive precursor material in order to highlight the effects of carrier gas composition (Ar/H2O, Ar/H2O/H2, and Ar/Air), temperature, the initial cesium/iodine (Cs/I) molar ratio by adding cesium hydroxide, and the presence of boron on the molar composition of the deposited iodine compound and on the release of gaseous iodine from the deposit. The results from the experiments involving only cesium iodide as a precursor revealed a slight decomposition of cesium iodide and a release of gaseous iodine. Furthermore, the measured gaseous iodine mass decreased with the addition of hydrogen to the carrier gas at 650°C. At 400°C, the amount of released material (aerosol and gas) was decreased. However, whereas at 650°C the sampled iodine existed mainly as aerosols, the mass concentration recorded from the experiment at 400°C indicated a predominance of gaseous iodine. When the initial Cs/I molar ratio was significantly greater than unity (1.5 < Cs/I < 4.5), the mass of produced gaseous iodine was barely detectable, suggesting a reaction between cesium hydroxide and the gaseous iodine released from cesium iodide decomposition. In the presence of boron, the transport of gaseous iodine was increased as a result of the formation of glassy cesium borate in the evaporation crucible. The presence of steam and its quantity were shown to have an enhancing influence on the cesium borate formation and on the release of gaseous iodine.