ICONE11-36183
Corrosion Properties of Japanese FBR Materials in Stagnant Pb-Bi at Elevated
Temperature
Authors
Tomohiro
Furukawa, Kazumi Aoto, Japan Nuclear Cycle Development Institute
Georg Mueller, Gustav Schumacher, Alfons
Weisenburger, Annette Heinzel, Research
Center Karlsruhe, Institute for Pulsed Power and Microwave Technology (IHM),
Germany
Abstract
One
of the main problems in the development of advanced heavy liquid metal cooled
fast reactor (HLMFR) systems is the compatibility of structural and fuel
cladding materials with potential coolants. Lead-bismuth eutectic (LBE) is
expected to be one promising candidate material for a coolant of HLMFR in the
Feasibility Study on Commercialized Fast Reactor Cycle Systems in Japan. In
order to investigate the corrosion resistance of three Japanese materials named
FBR grade type 316ss (316FR), high chromium type ferritic steel (12Cr-steel)
and oxide dispersion strengthened martensitic type steel (ODS-M), corrosion
tests were carried out in stagnant LBE of 500°C to 650°C for 800h and 2,000h
under oxygen control at 10-6 weight percent by H2/H2O mixture gas flow.
According to thermodynamic calculation, oxide layer is formed on the surface at
the oxygen potential, and it was estimated that the base metal is protected
from the attack of LBE i.e. solution of metal elements to LBE. After the tests,
cross sections of the specimens were observed using scanning electron
microscopy with energy dispersive X-ray analyzer (SEM-EDX). It was confirmed
that the oxide layers were formed on the surface of all specimens, however, the
composition differed with testing temperature. The surface of the specimens
tested at 550°C or below was covered with two oxide layers. The main elements
of inner layer were Fe, Cr and O, and those of outer layer were Fe and O.
Although there were exfoliations at the outer layer, base metals were protected
by inner layer. From the results, it was considered that three steel showed
satisfying protection behavior at 550°C or below. On the other hand, the surface
tested in LBE at 600°C or more was only covered a thin layer, and the elements
were the same as those of inner layer tested at no more than 550°C. Most of the
oxide on the surface seems to exfoliate into LBE during test period, because
the thickness of the layer of the region exposed in LBE was smaller that of the
exposed at gas atmosphere at the same oxygen potential. In addition, there were
attacks of LBE on singular spots at the surface of three materials. The
phenomena were observed after 800h exposure for 316FR and ODS-M, and after
2,000h for 12Cr-steel.