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Remembering ANS member Gil Brown
Brown
The nuclear community is mourning the loss of Gilbert Brown, who passed away on July 11 at the age of 77 following a battle with cancer.
Brown, an American Nuclear Society Fellow and an ANS member for nearly 50 years, joined the faculty at Lowell Technological Institute—now the University of Massachusetts–Lowell—in 1973 and remained there for the rest of his career. He eventually became director of the UMass Lowell nuclear engineering program. After his retirement, he remained an emeritus professor at the university.
Sukesh Aghara, chair of the Nuclear Engineering Department Heads Organization, noted in an email to NEDHO members and others that “Gil was a relentless advocate for nuclear energy and a deeply respected member of our professional community. He was also a kind and generous friend—and one of the reasons I ended up at UMass Lowell. He served the university with great dedication. . . . Within NEDHO, Gil was a steady presence and served for many years as our treasurer. His contributions to nuclear engineering education and to this community will be dearly missed.”
C. Mun, L. Cantrel, C. Madic
Nuclear Technology | Volume 164 | Number 2 | November 2008 | Pages 245-254
Technical Paper | Reactor Safety | doi.org/10.13182/NT08-A4023
Articles are hosted by Taylor and Francis Online.
In the case of a hypothetical severe accident in a nuclear pressurized water reactor, the formation of radiotoxic RuO4(g) may occur in the reactor containment building, resulting from the interactions of ruthenium oxide deposits with the oxidizing medium induced by air radiolysis. Consequently, this gaseous ruthenium tetroxide may be dispersed into the environment; therefore, the determination of the ruthenium deposits behavior is of primary importance for nuclear safety studies. An experimental study, performed by the French Institut de Radioprotection et de Sûreté Nucléaire (IRSN), using a gamma irradiator cell (EPICUR facility at IRSN/Cadarache) has been carried out in order to obtain experimental data on these interactions. The results showed that radiolytic oxidation of ruthenium oxide deposits leads to the formation of gaseous ruthenium tetroxide to a significant extent. A comparison between the revolatilized Ru fractions obtained experimentally and those obtained by calculations based on the rate laws modeling ozone irradiation effect, established in previous studies, is presented. The disagreement observed is discussed. It appears that the oxidation resulting from air/steam radiolysis products is enhanced in comparison with pure ozone effect.
