4.7 Article

Selective capture of thallium(I) ion from aqueous solutions by amorphous hydrous manganese dioxide

Journal

CHEMICAL ENGINEERING JOURNAL
Volume 239, Issue -, Pages 200-206

Publisher

ELSEVIER SCIENCE SA
DOI: 10.1016/j.cej.2013.11.010

Keywords

Hydrous manganese dioxide; Thallium; Removal; Selectivity

Funding

  1. Program for National Natural Science Foundation of China [21177059/51078179]
  2. Natural Science Research Project of Huangshan University [2013xkj003]
  3. Natural Science Foundation of Anhui Education Department [KJ2012A259]

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Thallium, a highly toxic pollutant, has greater toxicity to mammals than common heavy metals such as lead, cadmium, mercury and efficient techniques for its removal are penurious. In the present study, amorphous hydrous manganese dioxide (HMO), an excellent sorbent for heavy metals retention, was synthesized by using oxidation and chemical precipitation method and its selective adsorption behavior toward Tl(1) was evaluated. The uptake of Tl(I) onto HMO is pH-dependent and dropped significantly with the pH rise from 2 to 4, and then followed by rapid promotion with further increased pH to 7. XPS spectrum analysis confirmed that more than half of the adsorbed Tl(1) was oxidized to insoluble Tl(III) in low pH range (2.02), while little adsorbed TO) was oxidized around neutral pH range (5.83). Compared to a macroporous cation exchanger D-001 and an metal-specific chelating resin Amberlite IRC-748, HMO exhibited stronger adsorption selectivity toward Tl(1) in the presence of high concentrations of competing Ca(11). In addition, the sorption of TO) onto HMO is fast and the kinetic data could be reasonably fitted by the pseudo-first-order model. The exhausted HMO particles could be efficiently regenerated by NaOH-NaOCl binary solution of alkalinity at 7.8% and active chlorine at 5.0%. All results presented strongly indicated that amorphous HMO is a sorbent of great potential for selective Tl(1) removal from contaminated waters. (C) 2013 Elsevier B.V. All rights reserved.

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