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Title: Understanding of a Novel Irradiation-induced Nanostructuring Process in SiC layer of TRISO fuel particles via Transmission Electron Microscopy

Conference ·

Metallic fission products are found to transport through the SiC layer of the tristructural isotropic (TRISO) nuclear fuel particle and various studies have been undertaken to understand the transport behavior [1, 2]. While the grain boundaries in SiC acts as a primary pathway to dissipate fission products in the form of multi-phased complex compounds, intragranular fission product precipitation has always been observed. Research on neutron irradiation damage tolerance of silicon carbide (SiC) and its composites, used in TRISO fuel, light water reactors (LWR) fuel cladding etc., has traditionally ignored the irradiation-induced “polymorphism” of SiC. In the post-irradiation advanced microscopy effort at Idaho National Laboratory, it has been recently discovered that the intragranular precipitation of fission products in SiC layer of TRISO coated fuels takes place via a dual step nucleation mechanism that involves cubic (?) ?hexagonal (?) SiC polymorphic transition, and subsequent metamorphosis of ?-SiC into fission product precipitates, as shown in Figure 1 [3]. This precipitation behavior cannot be explained by any reported nucleation mechanism. The extent of this precipitation has been observed to be influenced by the nature of the neutron irradiation induced damage structures. These damage structures (e.g., defect morphology and density) are also indicative of the irradiation temperature and neutron fluence levels experimented by the individual TRISO particles. The distinction of neutron irradiation damage structures as a function of the fuel kernel type, burn up level and fabrication histories of TRISO coated particles from the Advanced Gas reactor (AGR-1 and AGR-2) experiments has been examined and compared. This discovery not only adds new fundamental understanding of physical behavior of polymorphic ceramics under irradiation, but also provides the following beneficial traits for high temperature applications. 1) Since the extent of precipitation of the desired phase is directly dependent on the amount of precursor phase, the volume fraction of desired phase can be easily controlled by irradiation parameters. This eliminates the conventional limitation of volume fraction of a desired phase in the system as outlined by the phase diagram of the specific system. 2) Most of the precipitate-strengthened materials for high temperature applications suffer from degradation of size and shape of precipitate upon prolonged thermal exposures. But, precipitates are confined to the shape and size of the morphological template of surrogate phase (e.g. a Pd silicide precipitate is confined by the ?-SiC as shown in Figure 1(c)) in the present nucleation pathway. Hence, there is no possibility of desired phase to undergo any morphological degradation at high temperature that eventually will extend the lifetime of these materials at high temperature.

Research Organization:
Idaho National Lab. (INL), Idaho Falls, ID (United States)
Sponsoring Organization:
USDOE Office of Nuclear Energy (NE)
DOE Contract Number:
AC07-05ID14517
OSTI ID:
1478776
Report Number(s):
INL/CON-18-44674-Rev001
Resource Relation:
Journal Volume: 24; Journal Issue: S1; Conference: TMS2019, San Antonio Texas, 03/10/2019 - 03/14/2019
Country of Publication:
United States
Language:
English