4.7 Article

Electrolytic manganese residue disposal based on basic burning raw material: Heavy metals solidification/stabilization and long-term stability

Journal

SCIENCE OF THE TOTAL ENVIRONMENT
Volume 825, Issue -, Pages -

Publisher

ELSEVIER
DOI: 10.1016/j.scitotenv.2022.153774

Keywords

Electrolytic manganese residue; Basic burning raw material; Heavy metals; Ammonium; Long-term stable storage

Funding

  1. National Key Research and Development [2018YFC1903500]
  2. National Natural Science Foundation of China [21806132, 52174386]
  3. Sichuan Province Science and Technology Plan-Key Research and Development [2021YFH0058]

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Solidification/stabilization is an effective method to treat electrolytic manganese residue (EMR), and the use of basic burning raw material (BRM) has been found to successfully solidify/stabilize EMR. This study explores the mechanisms behind the solidification/stabilization process, focusing on the behavior of Mn2+ and NH4+ ions, the characterization of hydrated BRM and S/S EMR, as well as the long-term leaching behavior and changes in phase and morphology. The results show that the S/S process enhances the long-term stability of EMR, with reduced leaching concentrations and migration of Mn2+ ions, and the solidification/stabilization of other heavy metals through substitution and encapsulation.
Solidification/stabilization (S/S) is an option for the treatment of electrolytic manganese residue (EMR). Basic burning raw material (BRM) could successfully solidify/stabilize EMR, though heavy metals S/S mechanism and long-term stability remain unclear. Herein, Mn2+ and NH4+ S/S behavior, hydrated BRM and S/S EMR characterization, Mn2+ longterm leaching behavior, phase and morphology changes for long-term leaching were discussed in detail to clarify these mechanisms. Mn2+ and NH4+ leaching concentrations as well as pH value in S/S EMR were respectively 0.02 mg/L, 0.68 mg/L and 8.75, meeting the regulations of Chinese standard GB 8978-1996. Long-term stability of EMR was significantly enhanced after S/S. Mn2+ leaching concentration, Mn2+ migration, Mn2+ cumulative release, Mn2+ apparent diffusion coefficient and conductivity of EMR reduced to 0.05 mg/L, 5.5 x 10(-6) mg/(m(2).s), similar to 9 mg/m(2), 6.30 x 10(-15) m(2)/s and 435 mu s/cm. Mechanism studies showed that the hydration of BRM forms OH-, calcium silicate hydrate gels (C-S-H) and ettringite. Therefore, during S/S process, NH4+ was escaped as NH3, Mn2+ was solidified/stabi-lized as tephroite (Mn2SiO4), johannsenite (CaMnSi2O6) and davreuxite (MnAl6Si4O17(OH)(2)), and Pb2+, Cu2+, Ni2+, Zn2+ were solidified/stabilized by C-S-H and ettringite via substitution and encapsulation. This study provides a good choice for EMR long-term stable storage.

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