Pulse radiolysis study on the reactivity of NO3˙ radical toward uranous(iv ), hydrazinium nitrate and hydroxyl ammonium nitrate at room temperature and at 45 °C
R Musat
1, 2, 3, 4
,
J. L. Marignier
1, 2, 3, 4
,
C. Le Naour
5, 6, 7, 8, 9, 10
,
Ivan Andreevich Denisov
1, 2, 3, 4
,
L. Venault
11
,
Ph Moisy
4, 11, 12, 13, 14, 15
,
Mehran Mostafavi
1, 2, 3, 4
3
91405 Orsay
|
4
FRANCE
|
5
6
Institut de Physique Nucléaire
10
91406 Orsay Cedex
|
12
CEA
13
DEN
14
DMRC
Publication type: Journal Article
Publication date: 2020-02-13
scimago Q2
wos Q2
SJR: 0.698
CiteScore: 5.3
Impact factor: 2.9
ISSN: 14639076, 14639084
PubMed ID:
32090224
Physical and Theoretical Chemistry
General Physics and Astronomy
Abstract
Concentrated nitric acid solutions subjected to radiation produce radicals of extreme importance in the reprocessing of spent nuclear fuel. Knowledge of the different rate constants of the reactions involved in this chemistry is needed to improve the efficiency of the process and to define safe operating practices. Pulse radiolysis measurements are performed to find the rate constant of the reaction between NO3˙ radicals and U(iv) in highly concentrated nitrate solution. The optimal stabilization conditions toward thermal oxidation are defined for the considered solutions at room temperature and at 45 °C by adding anti-nitrous agents such as hydrazinium nitrate (HN) and hydroxyl ammonium nitrate (HAN). The decay of the NO3˙ radical is monitored and its reaction rates with HN, HAN and U(iv) are found to be 1.3 × 105, 1.5 × 107 and 1.6 × 106 M-1 s-1 at room temperature. The latter value is more than 10 times lower than the one currently used in numerical codes for simulation of the long-term radiolytic degradation associated with the reprocessing and storage of spent nuclear waste. At 45 °C, conditions similar to the reprocessing of spent fuel, the values of the rate constants of NO3˙ radical toward HN, HAN and U(iv) increase and are found to be 2.6 × 105, 2.9 × 107 and 9.3 × 106 M-1 s-1.
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Total citations:
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Citations from 2024:
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(12.5%)
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Musat R. et al. Pulse radiolysis study on the reactivity of NO3˙ radical toward uranous(iv), hydrazinium nitrate and hydroxyl ammonium nitrate at room temperature and at 45 °C // Physical Chemistry Chemical Physics. 2020. Vol. 22. No. 9. pp. 5188-5197.
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Musat R., Marignier J. L., Le Naour C., Denisov I. A., Venault L., Moisy Ph., Mostafavi M. Pulse radiolysis study on the reactivity of NO3˙ radical toward uranous(iv), hydrazinium nitrate and hydroxyl ammonium nitrate at room temperature and at 45 °C // Physical Chemistry Chemical Physics. 2020. Vol. 22. No. 9. pp. 5188-5197.
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TY - JOUR
DO - 10.1039/C9CP07034F
UR - https://xlink.rsc.org/?DOI=C9CP07034F
TI - Pulse radiolysis study on the reactivity of NO3˙ radical toward uranous(iv), hydrazinium nitrate and hydroxyl ammonium nitrate at room temperature and at 45 °C
T2 - Physical Chemistry Chemical Physics
AU - Musat, R
AU - Marignier, J. L.
AU - Le Naour, C.
AU - Denisov, Ivan Andreevich
AU - Venault, L.
AU - Moisy, Ph
AU - Mostafavi, Mehran
PY - 2020
DA - 2020/02/13
PB - Royal Society of Chemistry (RSC)
SP - 5188-5197
IS - 9
VL - 22
PMID - 32090224
SN - 1463-9076
SN - 1463-9084
ER -
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BibTex (up to 50 authors)
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@article{2020_Musat,
author = {R Musat and J. L. Marignier and C. Le Naour and Ivan Andreevich Denisov and L. Venault and Ph Moisy and Mehran Mostafavi},
title = {Pulse radiolysis study on the reactivity of NO3˙ radical toward uranous(iv), hydrazinium nitrate and hydroxyl ammonium nitrate at room temperature and at 45 °C},
journal = {Physical Chemistry Chemical Physics},
year = {2020},
volume = {22},
publisher = {Royal Society of Chemistry (RSC)},
month = {feb},
url = {https://xlink.rsc.org/?DOI=C9CP07034F},
number = {9},
pages = {5188--5197},
doi = {10.1039/C9CP07034F}
}
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MLA
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Musat, R., et al. “Pulse radiolysis study on the reactivity of NO3˙ radical toward uranous(iv), hydrazinium nitrate and hydroxyl ammonium nitrate at room temperature and at 45 °C.” Physical Chemistry Chemical Physics, vol. 22, no. 9, Feb. 2020, pp. 5188-5197. https://xlink.rsc.org/?DOI=C9CP07034F.