On the oxidation and ignition of uranium carbide fragments in air and comparison with zirconium carbide oxidation

Allbwn ymchwil: Cyfraniad at gyfnodolynErthygladolygiad gan gymheiriaid

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On the oxidation and ignition of uranium carbide fragments in air and comparison with zirconium carbide oxidation. / Gasparrini, C.; Podor, R.; Fiquet, O. et al.
Yn: Journal of Nuclear Materials, Cyfrol 592, 154944, 15.04.2024.

Allbwn ymchwil: Cyfraniad at gyfnodolynErthygladolygiad gan gymheiriaid

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Gasparrini C, Podor R, Fiquet O, Rushton MJD, Lee WE. On the oxidation and ignition of uranium carbide fragments in air and comparison with zirconium carbide oxidation. Journal of Nuclear Materials. 2024 Ebr 15;592:154944. Epub 2024 Chw 1. doi: 10.1016/j.jnucmat.2024.154944

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Gasparrini, C. ; Podor, R. ; Fiquet, O. et al. / On the oxidation and ignition of uranium carbide fragments in air and comparison with zirconium carbide oxidation. Yn: Journal of Nuclear Materials. 2024 ; Cyfrol 592.

RIS

TY - JOUR

T1 - On the oxidation and ignition of uranium carbide fragments in air and comparison with zirconium carbide oxidation

AU - Gasparrini, C.

AU - Podor, R.

AU - Fiquet, O.

AU - Rushton, M.J.D.

AU - Lee, W.E.

PY - 2024/4/15

Y1 - 2024/4/15

N2 - Oxidation of uranium carbide (UC) small fragments from sintered pellets was experimentally tested to better understand UC safe-handling procedures given the renewed interest of non-oxide fuels for high temperature gas or liquid metal cooled reactors. Transformation from UC to U3O8 via a self-ignition reaction was observed at partial pressure of oxygen as low as 10 Pa. The heat output from UC self-ignition in fragments (not-free from UO2 contamination) previously stored in either air atmosphere or inert-atmosphere during a three months period was monitored at 973 K and 1073 K in air atmosphere in a TGA/DTA and no difference could be observed. Residual carbon content, measured as amorphous carbon, carbide or CO/CO2, decreased with exposition temperature in U3O8 resulting oxide, this is in contrast with zirconium carbide resulting oxide, ZrO2. Cracking and stresses accumulated in the oxide were highest for UC to U3O8 compared to UC to UO2 reactions and ZrC to ZrO2 reactions.

AB - Oxidation of uranium carbide (UC) small fragments from sintered pellets was experimentally tested to better understand UC safe-handling procedures given the renewed interest of non-oxide fuels for high temperature gas or liquid metal cooled reactors. Transformation from UC to U3O8 via a self-ignition reaction was observed at partial pressure of oxygen as low as 10 Pa. The heat output from UC self-ignition in fragments (not-free from UO2 contamination) previously stored in either air atmosphere or inert-atmosphere during a three months period was monitored at 973 K and 1073 K in air atmosphere in a TGA/DTA and no difference could be observed. Residual carbon content, measured as amorphous carbon, carbide or CO/CO2, decreased with exposition temperature in U3O8 resulting oxide, this is in contrast with zirconium carbide resulting oxide, ZrO2. Cracking and stresses accumulated in the oxide were highest for UC to U3O8 compared to UC to UO2 reactions and ZrC to ZrO2 reactions.

KW - Uranium carbide

KW - Zirconium carbide

KW - Ignition

KW - Pyrophoricity

KW - Oxidation

U2 - 10.1016/j.jnucmat.2024.154944

DO - 10.1016/j.jnucmat.2024.154944

M3 - Article

VL - 592

JO - Journal of Nuclear Materials

JF - Journal of Nuclear Materials

SN - 0022-3115

M1 - 154944

ER -