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Fe13Cr5Al4Mo合金在360 ℃、18.6 MPa LiOH水溶液中的腐蚀行为
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1.中广核研究院有限公司 核燃料与材料研究所 深圳;2.上海大学 材料研究所 上海;3.上海大学 微结构重点实验室 上海;4.上海大学材料研究所

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TL341; TG146.4+14

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Corrosion Behavior of Fe13Cr5Al4Mo Alloy in Lithiated Water at 360 ℃、18.6 MPa
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The Key Laboratory for Advance Micro-Analysis,Shanghai University

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    摘要:

    采用静态高压釜研究了Fe13Cr5Al4Mo合金在360 ℃、18.6 MPa 70 μL/L LiOH水溶液中的腐蚀行为,以评估其在高温高压水环境中的耐腐蚀性能。采用SEM、TEM、EDS等研究了Fe13Cr5Al4Mo合金腐蚀后的氧化膜显微组织及其演化行为。结果表明,Fe13Cr5Al4Mo合金在LiOH水溶液中表现为腐蚀失重,这与LiOH影响了Fe的氧化物溶解-再沉积过程有关。Fe13Cr5Al4Mo合金在LiOH水溶液中长期腐蚀形成的氧化膜主要由Fe(Cr,Al)2O4组成,靠近外表面存在少量Fe3O4。这层Fe(Cr,Al)2O4膜可以阻碍金属阳离子和氧离子在氧化膜内的扩散,进而延缓Fe13Cr5Al4Mo合金的进一步腐蚀。

    Abstract:

    The corrosion behavior of Fe13Cr5Al4Mo alloy in 70 μL/L LiOH aqueous solution at 360 °C,18.6 MPa was studied using a static autoclave to assess its corrosion resistance. The microstructure of the oxide film on the Fe13Cr5Al4Mo alloy after corrosion was investigated by SEM, TEM and EDS. The results show that the Fe13Cr5Al4Mo alloy exhibits corrosion weight loss in lithiated water, which is related to the dissolution-redeposition process of Fe oxide affected by LiOH. The oxide film formed on the alloy during the long-term corrosion in lithiated water is mainly composed of Fe(Cr,Al)2O4, and a small amount of Fe3O4 present near the outer surface. The Fe(Cr,Al)2O4 layer can hinder the diffusion of metal ions and oxygen ions within the oxide film, which in turn retards further corrosion of the alloy.

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马海滨,王皓瑜,张文怀,林晓冬,薛佳祥,任啟森,廖业宏,胡丽娟,孙蓉蓉,梁 雪,李毅丰,姚美意. Fe13Cr5Al4Mo合金在360 ℃、18.6 MPa LiOH水溶液中的腐蚀行为[J].稀有金属材料与工程,2024,53(7):2018~2024.[Ma HaiBin, Wang Haoyu, Zhang Wenhuai, Lin Xiaodong, Xue Jiaxiang, Ren QIsen, Liao Yehong, Hu Lijuan, Sun Rongrong, Liang Xue, Li Yifeng, YAO Meiyi. Corrosion Behavior of Fe13Cr5Al4Mo Alloy in Lithiated Water at 360 ℃、18.6 MPa[J]. Rare Metal Materials and Engineering,2024,53(7):2018~2024.]
DOI:10.12442/j. issn.1002-185X.20230289

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  • 收稿日期:2023-05-15
  • 最后修改日期:2023-07-06
  • 录用日期:2023-07-28
  • 在线发布日期: 2024-07-22
  • 出版日期: 2024-07-12