Thallium morphology analysis and advanced treatment process of thallium wastewater from lead-zinc smelter

被引:0
|
作者
Wang Y. [1 ,2 ]
Xu H. [1 ]
Fu J. [3 ]
Tong T. [1 ]
Lin Z. [1 ,2 ]
Chai L. [1 ,2 ]
Sun Z. [1 ,3 ]
机构
[1] School of Metallurgy and Environment, Central South University, Changsha
[2] Chinese National Engineering Research Center for Control and Treatment of Heavy Metals Pollution, Changsha
[3] School of Environmental and Safety Engineering, North University of China, Taiyuan
基金
中国博士后科学基金;
关键词
adsorption; lead-zinc smelting; morphological analysis; thallium-containing wastewater;
D O I
10.11817/j.issn.1672-7207.2023.02.009
中图分类号
学科分类号
摘要
The main valence states and existing forms of Tl in wastewater were analyzed by Factsage 8.0. MnO2 and Fe3O4@PB adsorbents were prepared and the effects of pH, initial concentration, adsorption time, adsorbent quality and coexisting ions on thallium adsorption in simulated water were investigated. The expanding experiments on the treatment of industrial thallium wastewater with adsorbents were carried out. The results show that Tl is mainly present in the wastewater as Tl+, and there is a small amount of [TlCl-4] in the homogenizing pool water. The thallium contents of the simulated water are reduced from 100 μg/L to 3.09 μg/L and to 2.97 μg/L using the Fe3O4@PB and MnO2 of 0.8 g/L, respectively, at the optimal pH after 10 min. The effect of coexistence ions Na+ and Cl− is negligible on the removal of thallium. The effluent concentration of thallium in homogenized pool water is less than 2 μg/L after 30 min at the optimal pH=5 using Fe3O4@PB as adsorbent. The effluent concentrations of thallium in recycle water No.1 and No.2 are both less than 2 μg/L after 30 min at the optimal pH using the Fe3O4@PB and MnO2 as adsorbent. © 2023 Central South University of Technology. All rights reserved.
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页码:485 / 494
页数:9
相关论文
共 25 条
  • [1] TIAN Caixing, ZHANG Baogang, BORTHWICK A G L, Et al., Electrochemical oxidation of thallium (I) in groundwater by employing single-chamber microbial fuel cells as renewable power sources, International Journal of Hydrogen Energy, 42, 49, pp. 29454-29462, (2017)
  • [2] ESCUDERO L B, WUILLOUD R G, OLSINA R A., Sensitive determination of thallium species in drinking and natural water by ionic liquid-assisted ion-pairing liquid-liquid microextraction and inductively coupled plasma mass spectrometry, Journal of Hazardous Materials, 244, 245, (2013)
  • [3] ARBAB-ZAVAR M H, CHAMSAZ M, ZOHURI G, Et al., Synthesis and characterization of nano-pore thallium (III) ion-imprinted polymer as a new sorbent for separation and preconcentration of thallium, Journal of Hazardous Materials, 185, 1, (2011)
  • [4] ANAGBOSO M U, TURNER A, BRAUNGARDT C., Fractionation of thallium in the Tamar Estuary, south west England, Journal of Geochemical Exploration, 125, (2013)
  • [5] LIU Juan, LI Nuo, ZHANG Weilong, Et al., Thallium contamination in farmlands and common vegetables in a pyrite mining city and potential health risks[J], Environmental Pollution, 248, pp. 906-915, (2019)
  • [6] AGUILAR-CARRILLO J, HERRERA L, GUTIERREZ E J, Et al., Solid-phase distribution and mobility of thallium in mining-metallurgical residues: environmental hazard implications[J], Environmental Pollution, 243, pp. 1833-1845, (2018)
  • [7] CRUZ-HERNANDEZ Y, RUIZ-GARCIA M, VILLALOBOS M, Et al., Fractionation and mobility of thallium in areas impacted by mining-metallurgical activities: identification of a water-soluble Tl(I) fraction[J], Environmental Pollution, 237, (2018)
  • [8] LIU Juan, WANG Jin, TSANG D C W, Et al., Emerging thallium pollution in China and source tracing by thallium isotopes[J], Environmental Science & Technology, 52, 21, pp. 11977-11979, (2018)
  • [9] LOPEZ-ARCE P, GARRIDO F, GARCIA-GUINEA J, Et al., Historical roasting of thallium- and arsenic-bearing pyrite: Current Tl pollution in the Riotinto Mine area[J], Science of the Total Environment, 648, pp. 1263-1274, (2019)
  • [10] JOHNSON R A., Process for catalytic conversion of Thallium (I) to Thallium (III), (1980)