Comparing CrN and TiN Coatings for Accident-Tolerant Fuels in PWR and BWR Autoclaves

被引:7
作者
Fazi, Andrea [1 ]
Lokhande, Pratik [2 ]
Lopes, Denise Adorno [3 ,4 ]
Stiller, Krystyna [1 ]
Andren, Hans-Olof [1 ]
Thuvander, Mattias [1 ]
机构
[1] Chalmers Univ Technol, Dept Phys, S-41296 Gothenburg, Sweden
[2] Chalmers Univ Technol, Dept Chem & Chem Engn, S-41296 Gothenburg, Sweden
[3] KTH Royal Inst Technol, S-11428 Stockholm, Sweden
[4] Westinghouse Elect Sweden AB, S-72163 Vasteras, Sweden
来源
JOURNAL OF NUCLEAR ENGINEERING | 2022年 / 3卷 / 04期
关键词
accident-tolerant fuel; CrN; TiN; nitride coating; autoclave corrosion testing; CORROSION-RESISTANCE; OXIDATION BEHAVIOR; HYDROTHERMAL CORROSION; TITANIUM NITRIDE; PARTIAL-PRESSURE; HARD COATINGS; THIN-FILMS; CHROMIUM; ALLOY; DIAGRAMS;
D O I
10.3390/jne3040019
中图分类号
TL [原子能技术]; O571 [原子核物理学];
学科分类号
0827 ; 082701 ;
摘要
The development of coatings for accident-tolerant fuels (ATFs) for light water reactor (LWR) applications promises improved corrosion resistance under accident conditions and better performances during operation. CrN and TiN coatings are characterized by high wear resistance coupled with good corrosion resistance properties. They are generally used to protect materials in applications where extreme conditions are involved and represent promising candidates for ATF. Zr cladding tubes coated with 5 mu m-thick CrN or TiN, exposed in an autoclave to simulated PWR chemistry and BWR chemistry, were characterized with SEM, EDS, and STEM. The investigation focused on the performance and oxidation mechanisms of the coated claddings under simulated reactor chemistry. Both coatings provided improved oxidation resistance in a simulated PWR environment, where passivating films of Cr2O3 and TiO2, less than 1 mu m-thick, formed on the CrN and TiN outer surfaces, respectively. Under the more challenging BWR conditions, any formed Cr2O3 dissolved into the oxidizing water, resulting in the complete dissolution of the CrN coating. For the TiN coating, the formation of a stable TiO2 film was observed under BWR conditions, but the developed oxide film was unable to stop the flux of oxygen to the substrate, causing the oxidation of the substrate.
引用
收藏
页码:321 / 332
页数:12
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