Reduction Kinetics of Hematite Powder in Hydrogen Atmosphere at Moderate Temperatures

被引:41
作者
Chen, Zhiyuan [1 ]
Dang, Jie [2 ,3 ]
Hu, Xiaojun [4 ]
Yan, Hongyan [5 ]
机构
[1] Delft Univ Technol, Dept Mat Sci & Engn, Mekelweg 2, NL-2628 CD Delft, Netherlands
[2] Chongqing Univ, Coll Mat Sci & Engn, Chongqing 400044, Peoples R China
[3] Chongqing Univ, Chongqing Key Lab Vanadium Titanium Met & New Mat, Chongqing 400044, Peoples R China
[4] Univ Sci & Technol Beijing, State Key Lab Adv Met, Beijing 100083, Peoples R China
[5] North China Univ Sci & Technol, Coll Met & Energy, 21 Bohai Rd, Caofeidian Xincheng 063210, Tangshan, Peoples R China
来源
METALS | 2018年 / 8卷 / 10期
基金
国家重点研发计划; 中国国家自然科学基金;
关键词
iron oxides; hydrogen; direction reduction; kinetics; IRON-OXIDES; ACTIVATION-ENERGY; MAGNETITE CONCENTRATE; GASEOUS REDUCTION; CARBON-MONOXIDE; CO2; EMISSIONS; WUSTITE; ORE; MECHANISMS; H-2;
D O I
10.3390/met8100751
中图分类号
T [工业技术];
学科分类号
08 ;
摘要
Hydrogen has received much attention in the development of direct reduction of iron ores because hydrogen metallurgy is one of the effective methods to reduce CO2 emission in the iron and steel industry. In this study, the kinetic mechanism of reduction of hematite particles was studied in a hydrogen atmosphere. The phases and morphological transformation of hematite during the reduction were characterized using X-ray diffraction and scanning electron microscopy with energy dispersive spectroscopy. It was found that porous magnetite was formed, and the particles were degraded during the reduction. Finally, sintering of the reduced iron and wustite retarded the reductive progress. The average activation energy was extracted to be 86.1 kJ/mol and 79.1 kJ/mol according to Flynn-Wall-Ozawa (FWO) and Starink methods, respectively. The reaction fraction dependent values of activation energy were suggested to be the result of multi-stage reactions during the reduction process. Furthermore, the variation of activation energy value was smoothed after heat treatment of hematite particles.
引用
收藏
页数:10
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