Solid state reduction of Panzhihua titanomagnetite concentrates with pulverized coal

被引:175
|
作者
Chen, De-sheng [1 ,2 ,3 ]
Song, Bo [2 ]
Wang, Li-na [1 ,3 ]
Qi, Tao [1 ,3 ]
Wang, Yong [1 ,3 ]
Wang, Wei-jing [1 ,3 ]
机构
[1] Chinese Acad Sci, Key Lab Green Proc & Engn, Inst Proc Engn, Beijing 100190, Peoples R China
[2] Univ Sci & Technol Beijing, Sch Met & Ecol Engn, Beijing 100083, Peoples R China
[3] Natl Engn Lab Hydromet Cleaner Prod Technol, Beijing 100190, Peoples R China
基金
中国国家自然科学基金;
关键词
Reduction; Titanomagnetite concentrates; Pre-oxidation; Additive; Pulverized coal; TITANIFEROUS MAGNETITES; SOLVENT-EXTRACTION; LEACH LIQUORS; ILMENITE; TITANIUM; RECOVERY; CARBON;
D O I
10.1016/j.mineng.2011.03.018
中图分类号
TQ [化学工业];
学科分类号
0817 ;
摘要
Titanomagnetite concentrates and pre-oxidized titanomagnetite concentrates were reduced isothermally at 1000-1200 degrees C by pulverized coal. XRD, SEM and EDS were used to characterize the samples. The influence of reduction conditions on the metallization degree of the samples, such as reduction temperature, C/Fe molar ratio, pre-oxidation and additives were studied. It was found that the pre-oxidation and additives played a considerable role in the metallization degree of titanomagnetite concentrates. During the pre-oxidation of titanomagnetite concentrates in air, the magnetite was oxidized to hematite and ilmenite was oxidized to hematite-ilmenite solid solution, hematite and TiO2. The pre-oxidation destroyed the crystal lattice of raw titanomagnetite concentrates and formed pores in the particles, which accelerated the reduction process. The effect of different additives on the metallization degree of pre-oxidized titanomagnetite concentrates was also discussed. The results show that when 1.5 wt.% Na2CO3 is used as an additive, the metallization degree of pre-oxidized titanomagnetite concentrates reaches 96.4%, after heating for 1 h at 1200 degrees C. The final reduced sample was composed of metallic iron, pseudobrookite solid solution and TiO2. (C) 2011 Elsevier Ltd. All rights reserved.
引用
收藏
页码:864 / 869
页数:6
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