Dissolution behavior and porous kinetics of limonitic laterite during nitric acid atmospheric leaching

被引:23
作者
He, Fei [1 ,2 ,3 ]
Ma, Baozhong [1 ,2 ]
Wang, Chengyan [1 ,2 ]
Zuo, Yian [1 ,2 ]
Chen, Yongqiang [1 ,2 ]
机构
[1] Univ Sci & Technol Beijing, State Key Lab Adv Met, Beijing 100083, Peoples R China
[2] Univ Sci & Technol Beijing, Sch Met & Ecol Engn, Beijing 100083, Peoples R China
[3] BGRIMM Technol Grp, Beijing 100160, Peoples R China
基金
中国国家自然科学基金;
关键词
Limonitic laterite; Nitric acid atmospheric leaching; Dissolution behavior; Porous kinetic models; FLUID-SOLID REACTIONS; GOETHITE; PROTONATION; SURFACE; NICKEL; MODEL; FTIR;
D O I
10.1016/j.mineng.2022.107671
中图分类号
TQ [化学工业];
学科分类号
0817 ;
摘要
In our previous study, the mineral evolution and porous kinetics during nitric acid pressure leaching of limonitic laterite has been investigated. In order to optimize the nitric acid leaching technology, this paper investigated the dissolution behavior and porous kinetics of limonitic laterite during nitric acid atmospheric leaching. The experimental results showed that Ni and Fe had consistent leaching behavior, whereas Co was only consistent with Mn in the early stages of leaching. The DFT (Density functional theory) simulations of goethite dissolution revealed that H+ attacked the bridging O first with adsorption energy of -1.37 eV, while NO3- attacked the Fe with adsorption energy of -3.07 eV, hence promoting the dissolution of Fe from the goethite crystals. Based on meticulous modeling analysis, the leaching of Ni could be described by grain model-cylindrical particle. In the early stage of leaching, the Ni extraction is regulated by chemical reactions with an activation energy of 88.4 kJ/mol. In the latter stage, the leaching is regulated by pore diffusion with an effective diffusivity of 1.37 x 10(-11) m(2)/min at 90 C. This study clarified the dissolution behavior of limonitic laterite, and described nickel leaching using a porous kinetic model.
引用
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页数:10
相关论文
共 31 条
[1]  
Ayanda O S., 2011, Journal of Minerals Materials Characterization Engineering, V10, P1457
[2]  
BHATIA SK, 1980, AICHE J, V26, P379, DOI 10.1002/aic.690260308
[3]   On the protonation of oxo- and hydroxo-groups of the goethite (α-FeOOH) surface:: A FTIR spectroscopic investigation of surface O-H stretching vibrations [J].
Boily, Jean-Francois ;
Felmy, Andrew R. .
GEOCHIMICA ET COSMOCHIMICA ACTA, 2008, 72 (14) :3338-3357
[5]   SPECIAL POINTS FOR BRILLOUIN-ZONE INTEGRATIONS [J].
CHADI, DJ .
PHYSICAL REVIEW B, 1977, 16 (04) :1746-1747
[6]   KINETICS AND MECHANISMS OF ACID DISSOLUTION OF GOETHITE ALPHA-FEOOH) [J].
CORNELL, RM ;
POSNER, AM ;
QUIRK, JP .
JOURNAL OF INORGANIC & NUCLEAR CHEMISTRY, 1976, 38 (03) :563-567
[7]   CRYSTAL MORPHOLOGY AND DISSOLUTION OF GOETHITE [J].
CORNELL, RM ;
POSNER, AM ;
QUIRK, JP .
JOURNAL OF INORGANIC & NUCLEAR CHEMISTRY, 1974, 36 (09) :1937-1946
[8]  
CORNELL RM, 1975, J APPL CHEM BIOTECHN, V25, P701
[9]   Insights into the dissolution kinetics of thermally activated serpentine for CO2 sequestration [J].
Farhang, F. ;
Rayson, M. ;
Brent, G. ;
Hodgins, T. ;
Stockenhuber, M. ;
Kennedy, E. .
CHEMICAL ENGINEERING JOURNAL, 2017, 330 :1174-1186
[10]   Asbestos health hazard: A spectroscopic study of synthetic geoinspired Fe-doped chrysotile [J].
Foresti, Elisabetta ;
Fornero, Elisa ;
Lesci, Isidoro Giorgio ;
Rinaudo, Caterina ;
Zuccheri, Tommaso ;
Roveri, Norberto .
JOURNAL OF HAZARDOUS MATERIALS, 2009, 167 (1-3) :1070-1079