Influences of oxygen on corrosion characteristics of TiO2/316L stainless steel in supercritical water

被引:7
作者
Wang, Yuzhen [1 ]
Liu, Zhuan [1 ]
Zhang, Xiaoqiang [1 ]
Gao, Fen [1 ]
Yang, Jianqiao [2 ]
Fang, Changqing [1 ]
Xu, Donghai [2 ]
Wang, Shuzhong [2 ]
机构
[1] Xian Univ Technol, Xian 710048, Shaanxi, Peoples R China
[2] Xi An Jiao Tong Univ, Key Lab Thermofluid Sci & Engn MOE, Xian 710049, Shaanxi, Peoples R China
基金
中国国家自然科学基金;
关键词
Supercritical water; Oxygen; Coating; 316L stainless steel; TiO2; Corrosion; FERRITIC-MARTENSITIC STEEL; HYDROGEN-PRODUCTION; BEHAVIOR; 316L; TEMPERATURE; OXIDATION; OXIDE; GASIFICATION; RESISTANCE; COATINGS;
D O I
10.1016/j.ijhydene.2018.11.074
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
Supercritical water gasification (SCWG) is a promising technology for converting organic wastes to hydrogen. Less amount of oxygen is beneficial for increasing hydrogen generation rate. However, the corrosion rate of reactor material would be accelerated. TiO2 coating with a thickness of 0.1 mm was prepared on the surface of 316L stainless steel (SS316L) to improve its corrosion resistance in supercritical water (SCW). The corrosion performances of TiO2/SS316L were tested in a bath SCW reactor at 400 degrees C, 25 MPa. The influences of oxygen concentration (0-1000 mg/L) on surface morphologies and corrosion depths were studied thoroughly. Results indicated that the surface of TiO2/SS316L exhibited cracks and pores after exposed in SCW. And the average corrosion rates accelerated at higher oxygen concentrations. The interface between the coating and medium was relatively smooth and there was no obvious change in the thickness of the coating with oxygen concentration of 0 and 500 mg/L. While for that with 1000 mg/L oxygen, the surface of TiO2/SS316L exhibited reticulate crack. The cross section showed a serrate structure, and only 0.08 mm thick of the coating was remained. In addition, the corrosion mechanism of coating was discussed. (C) 2018 Hydrogen Energy Publications LLC. Published by Elsevier Ltd. All rights reserved.
引用
收藏
页码:5099 / 5107
页数:9
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