TY - JOUR
T1 - Measurement methods for surface oxides on SUS 316L in simulated light water reactor coolant environments using synchrotron XRD and XRF
AU - Watanabe, Masashi
AU - Yonezawa, Toshio
AU - Shobu, Takahisa
AU - Shoji, Tetsuo
N1 - Funding Information:
The synchrotron X-rays measurements were performed at the SPring-8 facility with the assistance of the Japan Synchrotron Radiation Research Institute (JASRI) and Japan Atomic Energy Agency (JAEA) (Proposal No. 2007B3772, 2008A3771, 2008B2090, 2008B1333, 2008B3772, 2009A1004, 2009A3787_2009A-E12, 2009B1022, 2009B3785_2009B-E14, 2010A3784_2010A-E07, 2010B3783_2010B-E07, 2011A1022, 2011A3783, 2011B1025 and 2011B3771). A part of these experiments was conducted as a Nanotechnology Support Project of the Ministry of Education, Culture, Sports, Science and Technology (Proposal No. 2007B3772, 2008A3771, 2008B3772 and 2011B3771).
Funding Information:
A part of this study was performed as a part of the PEACE-E and PEACE-E2 research programs which were financially supported by the Tokyo Electric Power Company, Kansai Electric Power Company, Tohoku Electric Power Company, Japan Atomic Power Company, Chubu Electric Power Company, Hitachi, MHI, Toshiba, IHI, EDF, SNPI and EPRI. Another part of this study was supported by JSPS KAKENHI Grant Number 22360396. The authors would like to acknowledge their financial support. The authors would also like to acknowledge technical discussions with Dr. Peter Scott, experimental supports by Dr. Osami Sakata (NIMS) and Dr. Hiroo Tajiri (JASRI).
PY - 2013
Y1 - 2013
N2 - Synchrotron X-ray diffraction (XRD) and X-ray fluorescent (XRF) measurement techniques have been used for non-destructive characterization of surface oxide films on Type 316L austenitic stainless steels that were exposed to simulated primary water environments of pressurized water reactors (PWR) and boiling water reactors (BWR). The layer structures of the surface spinel oxides were revealed ex situ after oxidation by measurements made as a function of depth. The layer structure of spinel oxides formed in simulated PWR primary water should normally be different from that formed in simulated BWR water. After oxidation in the simulated BWR environment, the spinel oxide was observed to contain NiFe 2O4 at shallow depths, and FeCr2O4 and Fe3O4 at deeper depths. By contrast, after oxidation in the simulated PWR primary water environment, a Fe3O4 type spinel was observed near the surface and FeCr2O4 type spinel near the interface with the metal substrate. Furthermore, by in situ measurements during oxidation in the simulated BWR environment, it was also demonstrated that the ratio between spinel and hematite Fe2O 3 can be changed depending on the water condition such as BWR normal water chemistry or BWR hydrogen water chemistry.
AB - Synchrotron X-ray diffraction (XRD) and X-ray fluorescent (XRF) measurement techniques have been used for non-destructive characterization of surface oxide films on Type 316L austenitic stainless steels that were exposed to simulated primary water environments of pressurized water reactors (PWR) and boiling water reactors (BWR). The layer structures of the surface spinel oxides were revealed ex situ after oxidation by measurements made as a function of depth. The layer structure of spinel oxides formed in simulated PWR primary water should normally be different from that formed in simulated BWR water. After oxidation in the simulated BWR environment, the spinel oxide was observed to contain NiFe 2O4 at shallow depths, and FeCr2O4 and Fe3O4 at deeper depths. By contrast, after oxidation in the simulated PWR primary water environment, a Fe3O4 type spinel was observed near the surface and FeCr2O4 type spinel near the interface with the metal substrate. Furthermore, by in situ measurements during oxidation in the simulated BWR environment, it was also demonstrated that the ratio between spinel and hematite Fe2O 3 can be changed depending on the water condition such as BWR normal water chemistry or BWR hydrogen water chemistry.
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U2 - 10.1016/j.jnucmat.2012.10.049
DO - 10.1016/j.jnucmat.2012.10.049
M3 - Article
AN - SCOPUS:84871758400
SN - 0022-3115
VL - 434
SP - 189
EP - 197
JO - Journal of Nuclear Materials
JF - Journal of Nuclear Materials
IS - 1-3
ER -