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What’s the most difficult question you’ve been asked as a maintenance instructor?
Blye Widmar
"Where are the prints?!"
This was the final question in an onslaught of verbal feedback, comments, and critiques I received from my students back in 2019. I had two years of instructor experience and was teaching a class that had been meticulously rehearsed in preparation for an accreditation visit. I knew the training material well and transferred that knowledge effectively enough for all the students to pass the class. As we wrapped up, I asked the students how they felt about my first big system-level class, and they did not hold back.
“Why was the exam from memory when we don’t work from memory in the plant?” “Why didn’t we refer to the vendor documents?” “Why didn’t we practice more on the mock-up?” And so on.
Dhanpat Rai, Richard G. Strickert, Gary L. McVay
Nuclear Technology | Volume 58 | Number 1 | July 1982 | Pages 69-76
Technical Paper | Radioactive Waste Managment | doi.org/10.13182/NT82-A32959
Articles are hosted by Taylor and Francis Online.
To help predict concentrations of neptunium leached from nuclear waste repositories in geologic environments, the solubility of neptunium in a neptunium-doped borosilicate glass, which simulates a high-level waste glass, was investigated. The concentrations of neptunium in solutions contacting the crushed doped glass were found to be controlled by a neptunium solid phase that is similar to crystal-line(c)´NpO2 in solubility. Thus, the maximum concentration of the neptunium leached from this waste form can be predicted from the solubility of NpO2(c). This conclusion is based on similar neptunium concentrations in solutions contacting neptunium-doped glass, neptunium-doped glass plus NpO2(c), and NpO2(c) alone, under controlled redox potentials and a range of pH values. The quinhydrone used in this study was found to be a very effective redox buffer (the approximate pe + pH = 11.8). The predictions based on the thermodynamic data and the solvent extraction tests showed Np(V) to be the primary oxidation state in solution.
