Please wait a minute...
Frontiers of Chemical Science and Engineering

ISSN 2095-0179

ISSN 2095-0187(Online)

CN 11-5981/TQ

Postal Subscription Code 80-969

2018 Impact Factor: 2.809

Front Chem Sci Eng    2013, Vol. 7 Issue (1) : 95-102    https://doi.org/10.1007/s11705-013-1317-6
RESEARCH ARTICLE
Oxidative leaching kinetics of molybdenum-uranium ore in H2SO4 using H2O2 as an oxidizing agent
T. A. Lasheen1(), M. E. El-Ahmady1, H. B. Hassib2, A. S. Helal1
1. Nuclear Materials Authority, Cairo, Egypt; 2. Chemistry Department, Faculty of Science, Cairo University, Giza, Egypt
 Download: PDF(248 KB)   HTML
 Export: BibTeX | EndNote | Reference Manager | ProCite | RefWorks
Abstract

The processing of molybdenum-uranium ore in a sulfuric acid solution using hydrogen peroxide as an oxidant has been investigated. The leaching temperature, hydrogen peroxide concentration, sulfuric acid concentration, leaching time, particle size, liquid-to-solid ratio and agitation speed all have significant effects on the process. The optimum process operating parameters were: temperature: 95°C; H2O2 concentration: 0.5 M; sulfuric acid concentration: 2.5 M; time: 2 h; particle size: 74 μm, liquid-to-solid ratio: 14 ∶ 1 and agitation speed: 600 rpm. Under these experimental conditions, the extraction efficiency of molybdenum was about 98.4%, and the uranium extraction efficiency was about 98.7%.

The leaching kinetics of molybdenum showed that the reaction rate of the leaching process is controlled by the chemical reaction at the particle surface. The leaching process follows the kinetic model 1 ? (1?X)1/3 = kt with an apparent activation energy of 40.40 kJ/mole. The temperature, concentrations of H2O2 and H2SO4 and the mesh size are the main factors that influence the leaching rate. The reaction order in H2SO4 was 1.0012 and in H2O2 it was 1.2544.

Keywords leaching of molybdenum      leaching of uranium      kinetics     
Corresponding Author(s): Lasheen T. A.,Email:lasheen_ta@yahoo.com   
Issue Date: 05 March 2013
 Cite this article:   
T. A. Lasheen,M. E. El-Ahmady,H. B. Hassib, et al. Oxidative leaching kinetics of molybdenum-uranium ore in H2SO4 using H2O2 as an oxidizing agent[J]. Front Chem Sci Eng, 2013, 7(1): 95-102.
 URL:  
https://academic.hep.com.cn/fcse/EN/10.1007/s11705-013-1317-6
https://academic.hep.com.cn/fcse/EN/Y2013/V7/I1/95
Fig.1  XRD spectrum of the working ore
Fig.1  XRD spectrum of the working ore
ConstituentComposition /wt-%
SiO280.0
Al2O32.1
Fe2O30.5
CaO2.8
MgO0.7
Na2O3.9
K2O4.8
MnO–*
TiO20.01
P2O5
LOI**3.1
Total97.9
Tab.1  Chemical composition of the molybdenum-uranium ore
ConstituentConcentration/ ppm
U500
Mo5000
Tab.2  Assay of uranium and molybdenum in the working ore
Fig.2  Effect of HSO concentration on the leaching efficiencies of uranium and molybdenum at 0.5 M HO, 95°C, 1 : 14 solid/liquid ratio, 2 h and 74 μm
Fig.2  Effect of HSO concentration on the leaching efficiencies of uranium and molybdenum at 0.5 M HO, 95°C, 1 : 14 solid/liquid ratio, 2 h and 74 μm
Fig.3  Effect of the HO concentration on the leaching efficiencies of uranium and molybdenum at 2.5 M HSO, 95°C, 1 ∶ 14 solid/liquid ratio, 2 h and 74 μm
Fig.3  Effect of the HO concentration on the leaching efficiencies of uranium and molybdenum at 2.5 M HSO, 95°C, 1 ∶ 14 solid/liquid ratio, 2 h and 74 μm
Fig.4  Effect of temperature upon the leaching efficiencies of uranium and molybdenum at 2.5 M HSO, 0.5 M HO, 1 ∶ 14 solid/liquid ratio, 2 h and 74 μm
Fig.4  Effect of temperature upon the leaching efficiencies of uranium and molybdenum at 2.5 M HSO, 0.5 M HO, 1 ∶ 14 solid/liquid ratio, 2 h and 74 μm
Fig.5  Effect of solid/liquid ratio upon the leaching efficiencies of uranium and molybdenum at 2.5 M HSO, 0.5 M HO, 95°C, 2 h and 74 μm
Fig.5  Effect of solid/liquid ratio upon the leaching efficiencies of uranium and molybdenum at 2.5 M HSO, 0.5 M HO, 95°C, 2 h and 74 μm
Fig.6  Effect of temperature on the leaching rate of molybdenum at 2.5 M HSO, 0.5 M HO and 74 μm
Fig.6  Effect of temperature on the leaching rate of molybdenum at 2.5 M HSO, 0.5 M HO and 74 μm
Fig.7  Relationship between [1 – (1–)] and leaching time for molybdenum leaching at various temperatures at 2.5 M HSO, 0.5 M HO and 74 μm
Fig.7  Relationship between [1 – (1–)] and leaching time for molybdenum leaching at various temperatures at 2.5 M HSO, 0.5 M HO and 74 μm
Fig.8  Arrhenius plot for molybdenum leaching at 2.5 M HSO, 0.5 M HO and 74 μm
Fig.8  Arrhenius plot for molybdenum leaching at 2.5 M HSO, 0.5 M HO and 74 μm
Fig.9  Effect of HSO concentration on the leaching rate of molybdenum at 0.5 M HO, 95°C and 74 μm
Fig.9  Effect of HSO concentration on the leaching rate of molybdenum at 0.5 M HO, 95°C and 74 μm
Fig.10  Relationship between [1 – (1 – )] and the leaching time for molybdenum leaching at various HSO concentrations at 0.5 M HO, 95°C and 74 μm
Fig.10  Relationship between [1 – (1 – )] and the leaching time for molybdenum leaching at various HSO concentrations at 0.5 M HO, 95°C and 74 μm
Fig.11  log-log plot of the rate constant versus total HSO concentration at 0.5 M HO, 95°C and 74 μm
Fig.11  log-log plot of the rate constant versus total HSO concentration at 0.5 M HO, 95°C and 74 μm
Fig.12  Effect of the HO concentration on the leaching rate of molybdenum at 2.5 M HSO, 95°C and 74 μm
Fig.12  Effect of the HO concentration on the leaching rate of molybdenum at 2.5 M HSO, 95°C and 74 μm
Fig.13  Relationship between [1 – (1 – )] and the leaching time for molybdenum leaching at various HO concentrations at 2.5 M HSO, 95°C and 74 μm
Fig.13  Relationship between [1 – (1 – )] and the leaching time for molybdenum leaching at various HO concentrations at 2.5 M HSO, 95°C and 74 μm
Fig.14  log-log plot of the rate constant versus total HO concentration at 2.5 M HSO, 95°C and 74 μm
Fig.14  log-log plot of the rate constant versus total HO concentration at 2.5 M HSO, 95°C and 74 μm
Fig.15  Effect of particle size on the leaching rate of molybdenum at 2.5 M HSO, 0.5 M HO and 95°C
Fig.15  Effect of particle size on the leaching rate of molybdenum at 2.5 M HSO, 0.5 M HO and 95°C
Fig.16  Relationship between [1 – (1 – )] and the leaching time for molybdenum leaching with different particle sizes at 2.5 M HSO, 0.5 M HO and 95°C
Fig.16  Relationship between [1 – (1 – )] and the leaching time for molybdenum leaching with different particle sizes at 2.5 M HSO, 0.5 M HO and 95°C
Fig.17  Plot of the rate constant versus the inverse of the particle diameter at 2.5 M HSO, 0.5 M HO and 95°C
Fig.17  Plot of the rate constant versus the inverse of the particle diameter at 2.5 M HSO, 0.5 M HO and 95°C
1 Wang M Y, Wang X W. Extraction of molybdenum and nickel from carbonaceous shale by oxidation roasting, sulphation roasting and water leaching. Hydrometallurgy , 2010, 102(1–4): 50–54
doi: 10.1016/j.hydromet.2010.02.001
2 Wang M Y, Wang X W, Liu W L. A novel technology of molybdenum extraction from low grade Ni-Mo ore. Hydrometallurgy , 2009, 97(1–2): 126–130
doi: 10.1016/j.hydromet.2008.12.004
3 Berg V D. Yang J A, Nauta M Y, Sandwijk H H K, Reuter V A. Comprehensive processing of low grade sulphidic molybdenum ores. Minerals Engineering , 2002, 15: 879–883
4 Khoshnevisan A, Yoozbashizadeh H, Mozammel M, Sadrnezhaad S K. Kinetics of pressure oxidative leaching of molybdenite concentrate by nitric acid. Hydrometallurgy , 2012, 111–112: 52–57
doi: 10.1016/j.hydromet.2011.10.002
5 Amer A. Hydrometallurgical processing of low grade Qattar molybdenite concentrate, Egypt. Erzmetall. Journal for Exploration. Mining and Metallurgy , 2001, 54(7–8): 381–385
6 Zhao Z W, Zhang G, Huo G S, Li H G. Kinetics of atmospheric leaching molybdenum from metalliferous black shales by air oxidation in alkali solution. Hydrometallurgy , 2009, 97(3–4): 233–236
doi: 10.1016/j.hydromet.2009.02.004
7 Vizsolyi A, Peters E. Nitric acid leaching of molybdenite concentrates. Hydrometallurgy , 1980, 6(1–2): 103–119
doi: 10.1016/0304-386X(80)90011-0
8 Valenzuela F R, Andrade J P, Sapag J, Tapia C, Basualto C. The solvent extraction separation of molybdenum and copper from acid leach residual solution of chilean molybdenite concentrate. Minerals Engineering , 1995, 8(8): 893–904
doi: 10.1016/0892-6875(95)00051-Q
9 Medvedev A S, Aleksandrov P V. Investigations on processing low-grade molybdenum concentrate by the nitric-acid method. Russian Journal of Non-Ferrous Metals , 2009, 50(4): 353–356
doi: 10.3103/S1067821209040087
10 Warren I H, Mounsey D M. Factors influencing the selective leaching of molybdenum with sodium hypochlorite from copper/molybdenum sulphide minerals. Hydrometallurgy , 1983, 10(3): 343–357
doi: 10.1016/0304-386X(83)90064-6
11 Liu Y C, Zhong H, Cao Z F. Molybdenum removal from copper ore concentrate by sodium hypochlorite leaching. Mining Science and Technology , 2011, 21: 61–64
12 Liu W P, Xu H, Yang X Y, Shi X C. Extraction of molybdenum from low-grade Ni-Mo ore in sodium hypochlorite solution under mechanical activation. Minerals Engineering , 2011, 24(14): 1580–1585
doi: 10.1016/j.mineng.2011.08.010
13 Barr D S, Lindstrom R E, Hendrix J L. Control of the chlorate factor in electrooxidation leaching of molybdenum concentrates. International Journal of Mineral Processing , 1975, 2(4): 303–320
doi: 10.1016/0301-7516(75)90025-3
14 Cao Z F, Zhong H, Liu G Y, Fu J G, Wen Z Q, Wang S. Electric-oxidation extractions of molybdenite concentrate in alkaline NaCl electrolyte. Journal of CentralβSouth UniversityβofβTechnology , 2010, 17(3): 480–484
doi: 10.1007/s11771-010-0510-8
15 Cao Z F, Zhong H, Liu G Y, Qiu Y R, Wang S. Molybdenum extraction from molybdenite concentrate in NaCl electrolyte. Journal of the Taiwan Institute of Chemical Engineers , 2010, 41(3): 338–343
doi: 10.1016/j.jtice.2009.11.007
16 Landa E R. Leaching of molybdenum and arsenic from uranium ore and mill tailings. Hydrometallurgy , 1984, 13(2): 203–211
doi: 10.1016/0304-386X(84)90027-6
17 Bartecki A, Rycerz L. Kinetics and mechanism of dissolution of synthetic molybdenum disulphide MoS2 in bromate solutions. Part II: Kinetics of molybdenum disulphide dissolution in the MoS2-KBrO3-H2SO4-H2O system. Hydrometallurgy , 1988, 20(2): 249–257
doi: 10.1016/0304-386X(88)90055-2
18 Bartecki A, Rycerz L. Kinetics and mechanism of dissolution of synthetic molybdenum disulphide MoS2 in bromate solutions. Part III: Mechanism of dissolution of molybdenum disulphide in bromate solutions. Hydrometallurgy , 1988, 20(2): 259–272
doi: 10.1016/0304-386X(88)90056-4
19 Antonijevic M M, Pacovic N V. Investigation of molybdenite oxidation by sodium dichromate. Minerals Engineering , 1992, 5(2): 223–233
doi: 10.1016/0892-6875(92)90044-A
20 Marczenko Z. Spectrophotometric Determination of Elements. New York: John Wiley and Sons, 1986, 107–640
21 Welz B, Sperling M. Atomic Absorption Spectrometry . 3rd ed. New York: Wiley-VCH Weinheim, 1999, 387–500
22 Biswas S, Pathak P N, Roy S B. Development of an extractive spectrophotometric method for estimation of uranium in ore leach solutions using 2-ethylhexyl phosphonic acid-mono-2-ethylhexyl ester (PC88A) and tri-n-octyl phosphine oxide (TOPO) mixture as extractant and 2-(5-bromo-2-pyridylozo)-5-diethyl aminophenol (Br-PADAP) as chromophore. Spectrochimica Acta Part A , 2012, 91: 222–227
doi: 10.1016/j.saa.2012.02.005
23 Cotton F A, Wilkinson G. Advanced Inorganic Chemistry. 5th ed. New York: Wiley, 1988, 456–458
24 Habashi F. Principles of Extractive Metallurgy, General Principles. Vol. 1. New York: Gordon and Breach, 1980, 111–252
25 Ray H S. Kinetics of metallurgical reactions. New Delhi: Oxford & IBHC, 1993, 1–75
[1] Xuantao Wu, Jie Wang. Intrinsic kinetics and external diffusion of catalytic steam gasification of fine coal char particles under pressurized and fluidized conditions[J]. Front. Chem. Sci. Eng., 2019, 13(2): 415-426.
[2] Shaojie Wang,Zhihong Ma,Ting Zhang,Meidan Bao,Haijia Su. Optimization and modeling of biohydrogen production by mixed bacterial cultures from raw cassava starch[J]. Front. Chem. Sci. Eng., 2017, 11(1): 100-106.
[3] Suvidha Gupta,R. A. Pandey,Sanjay B. Pawar. Microalgal bioremediation of food-processing industrial wastewater under mixotrophic conditions: Kinetics and scale-up approach[J]. Front. Chem. Sci. Eng., 2016, 10(4): 499-508.
[4] Jinbo OUYANG, Jingkang WANG, Yongli WANG, Qiuxiang YIN, Hongxun HAO. Thermodynamic study on dynamic water and organic vapor sorption on amorphous valnemulin hydrochloride[J]. Front. Chem. Sci. Eng., 2015, 9(1): 94-104.
[5] Farouq TWAIQ,M.S. NASSER,Sagheer A. ONAIZI. Effect of the degree of template removal from mesoporous silicate materials on their adsorption of heavy oil from aqueous solution[J]. Front. Chem. Sci. Eng., 2014, 8(4): 488-497.
[6] Weixin ZHANG, Wenran ZHAO, Zaoyuan ZHOU, Zeheng YANG. Facile synthesis of α-MnO2 micronests composed of nanowires and their enhanced adsorption to Congo red[J]. Front Chem Sci Eng, 2014, 8(1): 64-72.
[7] Tiantian LIU, Yuanyuan RAN, Bochao WANG, Weibing DONG, Songgu WU, Junbo GONG. The dehydration behavior and non-isothermal dehydration kinetics of donepezil hydrochloride monohydrate (Form I)[J]. Front Chem Sci Eng, 2014, 8(1): 55-63.
[8] Jasmin Shah, M. Rasul Jan, Attaul Haq, Younas Khan. Removal of Rhodamine B from aqueous solutions and wastewater by walnut shells: kinetics, equilibrium and thermodynamics studies[J]. Front Chem Sci Eng, 2013, 7(4): 428-436.
[9] Xingfu SONG, Kefeng TONG, Shuying SUN, Ze SUN, Jianguo YU. Preparation and crystallization kinetics of micron-sized Mg(OH)2 in a mixed suspension mixed product removal crystallizer[J]. Front Chem Sci Eng, 2013, 7(2): 130-138.
[10] Xingfu SONG, Jingcai ZHAO, Yunzhao LI, Ze SUN, Jianguo YU. Thermal decomposition mechanism of ammonium sulfate catalyzed by ferric oxide[J]. Front Chem Sci Eng, 2013, 7(2): 210-217.
[11] Hongman ZHANG, Qiang JIN, Rui XU, Lishi YAN, Zengxiang LIN. Kinetic studies of xylan hydrolysis of corn stover in a dilute acid cycle spray flow-through reactor[J]. Front Chem Sci Eng, 2011, 5(2): 252-257.
[12] Bingnan REN. Kinetics and thermodynamics of the phosphine adsorption on the modified activated carbon[J]. Front Chem Sci Eng, 2011, 5(2): 203-208.
[13] Zhen CHEN, Haitao ZHANG, Weiyong YING, Dingye FANG. Study on direct alcohol/ether fuel synthesis process in bubble column slurry reactor[J]. Front Chem Eng Chin, 2010, 4(4): 461-471.
[14] Tianlong DENG, Yafei GUO, Mengxia LIAO, Dongchan LI. Silver-catalyzed bioleaching for raw low-grade copper sulphide ores[J]. Front Chem Eng Chin, 2009, 3(3): 250-254.
[15] Zheng WANG, Zai-Sha MAO, Chao YANG, Qinghua ZHANG, Jingcai CHENG. Numerical investigation of the influence of kinetics and shape factor on barium sulfate precipitation in a continuous stirred tank[J]. Front Chem Eng Chin, 2009, 3(3): 272-281.
Viewed
Full text


Abstract

Cited

  Shared   
  Discussed