首页|Fe13Cr5Al4Mo 合金在 360 ℃/18.6 MPa LiOH水溶液中的腐蚀行为

Fe13Cr5Al4Mo 合金在 360 ℃/18.6 MPa LiOH水溶液中的腐蚀行为

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采用静态高压釜研究了 Fe13Cr5Al4Mo合金在360 ℃/18.6 MPa/70 μg/mL 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.
Corrosion Behavior of Fe13Cr5A14Mo Alloy in LiOH Aqueous Solution at 360 ℃/18.6 MPa
The corrosion behavior of Fe13Cr5A14Mo alloy in 70 μg/mL LiOH aqueous solution at 360 ℃/18.6 MPa was studied using a static autoclave to assess its corrosion resistance.The microstructure of the oxide film on the Fe13Cr5A14Mo alloy after corrosion was investigated by SEM,TEM and EDS.The results show that the Fe13Cr5A14Mo alloy exhibits corrosion mass loss in LiOH aqueous solution,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 LiOH aqueous solution is mainly composed of Fe(Cr,Al)2O4,and a small amount of Fe3O4 exists 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.

ATF cladding materialsFeCrAl alloycorrosionoxide filmmicrostructure

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

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中广核研究院有限公司,广东深圳 518026

上海大学材料研究所,上海 200072

上海大学微结构重点实验室,上海 200444

ATF包壳材料 FeCrAl合金 腐蚀 氧化膜 显微组织

2024

稀有金属材料与工程
中国有色金属学会,中国材料研究学会,西北有色金属研究院

稀有金属材料与工程

CSTPCD北大核心
影响因子:0.634
ISSN:1002-185X
年,卷(期):2024.53(7)