WANG Dong,ZHONG Ru-hao,ZHANG Ya-pei,GUO Chao,XU Hao-de,YU Jian,LAN Yi-cong,SU Guang-hui,QIU Sui-zheng,TIAN Wen-xi.High-temperature Steam Oxidation Behavior of Magnetron-sputtered Cr-coated Zr Alloy Cladding[J],52(11):258-268
High-temperature Steam Oxidation Behavior of Magnetron-sputtered Cr-coated Zr Alloy Cladding
Received:October 11, 2022  Revised:February 13, 2023
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DOI:10.16490/j.cnki.issn.1001-3660.2023.11.020
KeyWord:Zr alloy  Cr coating  accident tolerant fuel cladding  nuclear reactor accident  high-temperature steam  oxidation kinetics
                             
AuthorInstitution
WANG Dong School of Nuclear Science and Technology, Xi'an Jiaotong University, Xi'an , China
ZHONG Ru-hao China Nuclear Power Technology Research Institute, Guangdong Shenzhen , China
ZHANG Ya-pei School of Nuclear Science and Technology, Xi'an Jiaotong University, Xi'an , China
GUO Chao China Nuclear Power Technology Research Institute, Guangdong Shenzhen , China
XU Hao-de China Nuclear Power Technology Research Institute, Guangdong Shenzhen , China
YU Jian School of Nuclear Science and Technology, Xi'an Jiaotong University, Xi'an , China
LAN Yi-cong School of Nuclear Science and Technology, Xi'an Jiaotong University, Xi'an , China
SU Guang-hui School of Nuclear Science and Technology, Xi'an Jiaotong University, Xi'an , China
QIU Sui-zheng School of Nuclear Science and Technology, Xi'an Jiaotong University, Xi'an , China
TIAN Wen-xi School of Nuclear Science and Technology, Xi'an Jiaotong University, Xi'an , China
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Abstract:
      To improve the high-temperature oxidation resistance of Zr alloy cladding under nuclear accident conditions, Cr coating is proposed to be deposited on the cladding surface, which is one of the concepts of accident tolerant fuel (ATF) cladding. In this work, the oxidation behavior of magnetron-sputtered Cr-coated Zr-1Nb alloy cladding in 1 100-1 300 ℃ steam environment was studied. The cladding samples were 9.5 mm in outer diameter, 0.57 mm in thickness and 2 cm in length. Cr coating was deposited on the outer surface of the cladding tube. A horizontal tube furnace was used to carry out the tests. The test conditions included 1 100 ℃/3 600 s, 1 200 ℃/3 600 s, 1 300 ℃/1 800 s and 1 300 ℃/3 600 s. The samples experienced double-sided oxidation during the tests. Mass of the samples was measured by an analytical balance before and after the tests. Surface and cross-section morphologies of the samples were characterized by scanning electron microscopes (SEM). The element distribution was analyzed by energy dispersive spectroscopy (EDS). The as-deposited Cr coating was dense without obvious defects. After oxidation, stress existed in the Cr2O3 layer, which resulted in plastic deformation to form microscopic blisters or folds. If the stress could not be released in time by plastic deformation, micro-cracks appeared on the sample surfaces. Cr2O3 could further react with steam (containing small amount of dissolved O2) to generate volatile products, resulting in the formation of porous surface structure. After oxidation for 3 600 s at 1 100 ℃ and 1 200 ℃, the layered phases of Cr coating from outside to inside were Cr2O3, Cr and ZrCr2, which had a protective effect on the Zr substrate. ZrCr2 was formed by inter-diffusion between the metallic Cr and the Zr substrate. Zr diffused along the grain boundaries in metallic Cr. At 1 200 ℃/ 3 600 s, Zr reached the Cr2O3/Cr interface, and then Cr2O3 was reduced, leading to its local thinning. The diffusion resistance of O in Cr2O3 was reduced in the thinned region, thus resulting in an increased O flux from the Cr2O3/steam interface to the Cr2O3/Cr interface. The Zr combined with O to form ZrO2 precipitates in the grain boundaries of metallic Cr. ZrO2 precipitates acted as short-circuit paths for O to pass through the metallic Cr. Therefore, the amount of O absorbed by Zr substrate increased. After oxidation at 1 300 ℃ for 1 800 s, the degradation of Cr coating occurred and a thick ZrO2 layer grown under the coating. Due to the reduction reaction, the Cr2O3 layer was very thin. Zr was oxidized preferentially to Cr due to its larger oxygen affinity, hence a metallic Cr layer (containing ZrO2 precipitates) was retained. After oxidation for 3 600 s, with the thickening of ZrO2 layer, the metallic Cr was also completely oxidized. During the oxygen saturation of β-Zr and α-Zr(O), the parabolic rate constant for ZrO2 growth (kp) increased. Therefore, the experimental measurement of the thickness of inner ZrO2 layer deviated largely from the calculation by Cathcart-Pawel correlation in the case of 1 300 ℃/3 600 s. Due to the inner-sided oxidation of cladding samples, β-Zr substrate reached oxygen saturation rapidly, thus kp of the outer ZrO2 layer soon entered the secondary increase stage. Therefore, the outer ZrO2 layer had a higher growth rate than the inner one. According to the simulation results, the thickness of the inner and outer ZrO2 layers was reduced compared with the case without coating, indicating an improvement of oxidation resistance by Cr coating. The test conditions in this work are similar to state near the burst regions of cladding tubes during nuclear accidents, thus the results could have a reference value for accident management.
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