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North American construction is back—smaller and faster—at OPG’s Darlington
“The nuclear renaissance is real here,” said Ontario Power Generation’s Subo Sinnathamby on May 8, one year to the day after OPG secured a final investment decision to build the first of four planned BWRX-300 reactors at its Darlington nuclear power plant, and shortly after the new reactor’s foundation was lifted into place. “We got our license to construct in April and our [final investment decision] in May, and we’ve been off to the races since.”
Xiaohua Cao, Benfu Yang, Huajin Tan, Jingping Wan, Changyong Jiang
Fusion Science and Technology | Volume 41 | Number 3 | May 2002 | Pages 892-896
Material Interaction and Permeation | Proceedings of the Sixth International Conference on Tritium Science and Technology Tsukuba, Japan November 12-16, 2001 | doi.org/10.13182/FST02-A22713
Articles are hosted by Taylor and Francis Online.
The adsorption and desorption behaviors of tritium on the surfaces of stainless steel, copper, molybdenum and Kovar were studied. After the exposure in tritium gas ( 9 kPa gaseous tritium, 2 minutes exposure at 873 K and 40 minutes cooling ), the tritium desorbed at room temperature and during heating up to 1123 K and total sorbed tritium of the samples were measured. The results showed that the desorbed tritium at room temperature was only 1∼6% of total sorbed tritium and its amount order was: Kovar >copper > stainless steel > molybdenum. The total desorbed tritium was ranging from 2 to 22 MBq/cm2, the largest is for Kovar and the smallest is for stainless steel. The tritium released from these materials at room temperature and during heating was mostly in the form of HTO. The thermo-desorption spectra of these materials were obtained. It was found that at least 5, 3, 3, 4 sorption states of tritium exist in the exposed Kovar, molybdenum, copper and stainless steel samples respectively. Doping 1% hydrogen in the carrying gas of helium during the thermo-desorption had rather effect on this process.