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Devoted to all aspects of the nuclear fuel cycle including waste management, worldwide. Division specific areas of interest and involvement include uranium conversion and enrichment; fuel fabrication, management (in-core and ex-core) and recycle; transportation; safeguards; high-level, low-level and mixed waste management and disposal; public policy and program management; decontamination and decommissioning environmental restoration; and excess weapons materials disposition.
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Remembering Charles E. Till
Charles E. Till
Charles E. Till, an ANS member since 1963 and Fellow since 1987, passed away on March 22 at the age of 89. He earned bachelor’s and master’s degrees from the University of Saskatchewan and a Ph.D. in nuclear engineering from Imperial College, University of London. Till initially worked for the Civilian Atomic Power Department of the Canadian General Electric Company, where he was the physicist in charge of the startup of the first prototype CANDU reactor in Canada.
Till joined Argonne National Laboratory in 1963 in the Applied Physics Division, where he worked as an experimentalist in the Fast Critical Experiments program. He then moved to additional positions of increasing responsibility, becoming division director in 1973. Under his leadership, the Applied Physics Division established itself as one of the elite reactor physics organizations in the world. Both the experimental (critical experiments and nuclear data measurements) and nuclear analysis methods work were internationally recognized. Till led Argonne’s participation in the International Nuclear Fuel Cycle Evaluation (INFCE), and he was the lead U.S. delegate to INFCE Working Group 5, Fast Breeders.
Yasuhisa Oya, Misaki Sato, Hiromichi Uchimura, Naoko Ashikawa, Akio Sagara, Naoaki Yoshida, Yuji Hatano, Kenji Okuno
Fusion Science and Technology | Volume 67 | Number 3 | April 2015 | Pages 515-518
Proceedings of TRITIUM 2013 | doi.org/10.13182/FST14-T68
Articles are hosted by Taylor and Francis Online.
The effect of carbon implantation for the dynamic recycling of deuterium, which demonstrates tritium recycling, including retention and sputtering, was investigated using in-situ sputtered particle measurements. The C+ implanted W, WC and HOPG were prepared and dynamic sputtered particles were measured during H2 + irradiation. It was found that the major hydrocarbon species for C+ implanted tungsten was found to be CH3, although those for WC and HOPG were CH4. The chemical state of hydrocarbon is controlled by the H concentration in a W-C mixed layer. The amount of C-H bond and the retention of H trapped by carbon atom should control the chemical form of hydrocarbon sputtered by H2+ irradiation and the desorption of CH3 and CH2 was due to chemical sputtering, although that for CH was physical sputtering. The activation energy for CH3 desorption was estimated to be 0.4 eV, corresponding to the trapping process of hydrogen by carbon through the diffusion in W. It was concluded that the chemical states of hydrocarbon sputtered by H2+ irradiation for W was determined by the amount of C-H bond on the W surface.