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Corrosion evaluation of austenitic stainless steels in Li2CO3-K2CO3 eutectic salt for thermal energy storage
被引:1
|作者:
Xue, X. J.
[1
]
Dong, J.
[1
]
Zhao, C. Y.
[1
]
机构:
[1] Shanghai Jiao Tong Univ, Sch Mech & Power Engn, Inst Engn Thermophys, Shanghai 200240, Peoples R China
基金:
国家自然科学基金重大项目;
关键词:
Molten carbonate salt;
High temperature corrosion;
Stainless steel;
Pumped-thermal energy storage;
HIGH-TEMPERATURE CORROSION;
ALUMINA-FORMING ALLOYS;
CARBONATE MOLTEN-SALT;
HEAT-TRANSFER FLUIDS;
SOLAR POWER-PLANTS;
CHLORIDE SALTS;
RESISTANCE;
BEHAVIOR;
COATINGS;
NICKEL;
D O I:
10.1016/j.est.2024.113312
中图分类号:
TE [石油、天然气工业];
TK [能源与动力工程];
学科分类号:
0807 ;
0820 ;
摘要:
Molten carbonate salt is one of the promising candidates for high-temperature thermal energy storage tailored towards advanced pumped-thermal energy storage and next generation concentrated solar power technologies. However, severe corrosion of structural materials exposed to molten carbonate salts poses one of the most pivotal threats in terms of limiting their large-scale application at ever-escalating temperatures. Here, we elaborate the compatibility of three commercial austenitic stainless steels specifically SS310, SS316L and Incoloy 625 with Li2CO3-K2CO3 2 CO 3-K 2 CO 3 (28-72 wt%) eutectic salt. The corrosion behavior and corrosion mechanism of Fe-Cr (SS316L), Fe-Cr-Ni (SS310) and nickel-based (In625) alloys at 600 degrees C in air were also investigated. It revealed that SS310 exhibited better corrosion resistance compared to SS316 and In625, with weight loss of 23.8 mg/cm2 2 and corrosion rate of 522 mu m/year after 500 h of exposure at 600 degrees C. This implies that higher Ni content of the alloy may not necessarily improve the corrosion resistance, it is associated with the basicity of the molten and the solubility of Ni salt in the melt. ICP analysis indicated that the salts exposed to SS310 and In625 at the same exposure time both had nearly 11 times more Ni than that exposed to SS316. Precisely, it is related to the behavior of the Cr-enriched zones formed in the corrosion layers of different alloys. The corrosion mechanism of SS310 specimens in molten carbonate can be generally divided into the following steps: (i) selective oxidation of the metal elements and lithiation reactions of the metal oxides to generate a passivation scale, (ii) an evergrowing middle transition scale consisted of mixed metal oxides and lithium-containing compounds, (iii) cracking and peeling off of the corrosion scale.
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