1. Contribution of nitric acid and alcohol to the radiolytic degradation of TODGA in Isopar-M
- Author
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Yulia V. Serenko, Nikolay V. Yudin, Elena Belova, and Alexander V. Ponomarev
- Subjects
Health, Toxicology and Mutagenesis ,Radical ,Diglycolic acid ,Public Health, Environmental and Occupational Health ,Alcohol ,010403 inorganic & nuclear chemistry ,Photochemistry ,01 natural sciences ,Pollution ,Decomposition ,0104 chemical sciences ,Analytical Chemistry ,chemistry.chemical_compound ,Nuclear Energy and Engineering ,chemistry ,Nitric acid ,Radiolysis ,Alkoxy group ,Molecule ,Radiology, Nuclear Medicine and imaging ,Spectroscopy - Abstract
Radiolytic transformations of TODGA (N,N,N',N'-tetra-n-octylamide of diglycolic acid) in Isopar-M significantly depend both on the addition of alcohol (n-nonanol or n-decanol) and on the saturation of the solution with 8 M HNO3. Fragmentation of TODGA molecules is the dominant radiolytic process. Compared to acid-free solution, radiolysis in the presence of HNO3 results in a much lower yield of N,N-dioctylacetamide formation, while 2-hydroxy-N,N-dioctylacetamide remains the main degradation product of TODGA. The acidification of the solution promotes a lower radiolytic degradation of TODGA, but expands the range of final radiolysis products, in particular, due to the participation of NO2 and NO radicals in radiation-induced reactions. Alcohol serves as a source of alkoxy radicals, which are highly reactive towards TODGA. In the presence of nitric acid, a significant portion of alkoxy radicals decay in reactions with NO2, NO, and acyl radicals and, thus, do not participate in the decomposition of TODGA.
- Published
- 2021
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