The role of organic solvent radical cations in separations ligand degradation
Journal Article
·
· Journal of Radioanalytical and Nuclear Chemistry
- California State Univ. (CalState), Long Beach, CA (United States)
- Idaho National Lab. (INL), Idaho Falls, ID (United States)
- Brookhaven National Lab. (BNL), Upton, NY (United States)
The dodecane radical cation reaction rate constant with CMPO was measured using ps electron pulse radiolysis/absorption spectroscopy as k = (1.30 ± 0.11) x 1010 M-1 s-1 in dodecane/0.10 M CH2Cl2 solution. No reactivity increase occurred when these solutions were pre-contacted with nitric acid, similar to the behavior observed for TODGA. To corroborate these kinetic data with steady-state radiolysis measurements, where acid pre contacted CMPO showed significantly less degradation, it is proposed that the dodecane radical cation always reacts directly with TODGA, but for CMPO the charge-transfer occurs with the CMPO•HNO3 complex formed in the acid contacted solvent.
- Research Organization:
- Brookhaven National Lab. (BNL), Upton, NY (United States)
- Sponsoring Organization:
- USDOE Office of Science (SC), Basic Energy Sciences (BES)
- Grant/Contract Number:
- SC00112704
- OSTI ID:
- 1329809
- Report Number(s):
- BNL-112756-2016-JA; R&D Project: CO031; KC0304030
- Journal Information:
- Journal of Radioanalytical and Nuclear Chemistry, Vol. 307, Issue 3; ISSN 0236-5731
- Publisher:
- SpringerCopyright Statement
- Country of Publication:
- United States
- Language:
- English
Cited by: 16 works
Citation information provided by
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Web of Science
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