August 2017

Journal

Oxidation Behavior of Matrix Graphite and Its Effect on Compressive Strength

By:
Zhou, Xiangwen; Contescu, Cristian I; Zhao, Xi; Lu, Zhenming; Zhang, Jie; Kato, Yutai ; Wang, Yanli ; Liu, Bing; Tang, Yaping; Tang, Chunge
Journal Name:
Science and Technology of Nuclear Installations
Page Number:
1-6
Volume:
2017
Publication Date:
August 7, 2017
View DOI Listing:
https://doi.org/10.1155/2017/4275375

Abstract

Matrix graphite (MG) with incompletely graphitized binder used in high-temperature gas-cooled reactors (HTGRs) is commonly suspected to exhibit lower oxidation resistance in air. The oxidation performance of MG in both normal and off-normal events is important for the integrity evaluation and safety analysis of fuel elements in HTGR. In order to reveal the oxidation performance, the oxidation behavior of newly developed A3-3 MG at the temperature range from 500 to 950 °C in air was studied and the effect of oxidation at two typical temperatures on the compressive strength of oxidized MG specimens were characterized. Results show that temperature has a significant influence on the oxidation behavior of MG. The transition temperature between Regime I and II is ~700 °C and the activation energy (Ea) in Regime I is around 185 kJ/mol, a little lower than that of nuclear graphite, which indicates that MG is more vulnerable to oxidation. The mass-normalized oxidation rate in Regime I can be described as: ORm=2.59×109×exp(-22362.13/T) h-1. Oxidation at 550 °C in the kinetic regime causes more damages to compressive strength of MG than oxidation at 900 °C in the boundary layer control regime. Comparing with the strength of pristine MG specimens, the rate of compressive strength loss is 77.3% after oxidation at 550 °C and only 12.5% for oxidation at 900 °C. Microstructure images of SEM and porosity measurement by Mercury Porosimetry indicates that the significant compressive strength loss of MG oxidized at 550 °C in the kinetic regime may be attributed both the uniform pore formation throughout the bulk and the preferential oxidation of the binder.


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