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Chernobyl at 40 years: Looking back at Nuclear News
Sunday, April 26, at 1:23 a.m. local time will mark 40 years since the most severe nuclear accident in history: the meltdown of Unit 4 at the Chernobyl nuclear power plant in Ukraine, then part of the Soviet Union.
In the ensuing four decades, countless books, documentaries, articles, and conference sessions have examined Chernobyl’s history and impact from various angles. There is a similar abundance of outlooks in the archives of Nuclear News, where hundreds of scientists, advocates, critics, and politicians have shared their thoughts on Chernobyl over the years. Today, we will take a look at some highlights from the pages of NN to see how the story of Chernobyl evolved over the decades.
Sang Ge, Luo Xuejian, Liang HongWei, Sun Ying, Wu Sheng, Su Yongjun, Tu Mingjing, Luo Wenhua
Fusion Science and Technology | Volume 41 | Number 3 | May 2002 | Pages 758-763
Hydride and Storage | Proceedings of the Sixth International Conference on Tritium Science and Technology Tsukuba, Japan November 12-16, 2001 | doi.org/10.13182/FST02-A22688
Articles are hosted by Taylor and Francis Online.
In this paper, studies have been made concerning the poisoning mechanism. The processes of poisoning of LaNi47Al0.3 alloy are analyzed in detail by means of X-ray photoelectron spectroscopy (XPS), second ion mass spectroscopy (SIMS), Auger-energy spectroscopy (AES) and X-ray diffraction (XRD). The changes of the valence and the concentration distribution of the elements of the alloy LaNi4.7Al0.3 poisoned by CO are studied. The process and the mechanism of CO's poisoning of alloy LaNi47Al0.3 are proposed as follows: CO is absorbed on the surface of alloy, part of which reacts with La forming LaC2 and La2O3, or reacts with Ni forming NiO and C in the surface layer, the rest of the CO is decomposed into C and O, which diffuse into the bulk to react with La, Ni and Al. These results in phase-split reaction in surface layer of the particle, and enrichment of La and impoverishment Ni on the surface have taken place. The poisoning effect decreases with a increase of depth. The diffusion depth of C is within 600 Å in the surface layer, and that of O is within 1000 Å.The oxide film and carbonizing film prevent the H-storage alloys from further absorbing hydrogen, which leads to a deceleration of the H-storage capability. Moreover, The formation of a new phase with poor H-absorption capability is caused by the phase split reactions, which is one of reasons for the decrease of H-absorption property of the H-storage alloys.
