Selective recovery by precipitation of selenium and mercury from acid leaching solutions

  • D. D’Hondt
  • N. Gérain
  • A. Van Lierde

Synopsis

This paper concerns the hydrometallurgical treatment of lead, selenium and mercury muds coming from the gas cleaning stage of zinc sulfide concentrates roasting. In a first step, the muds are leached at a pulp dilution of 250 g/l and a temperature of 90°C with a 150–200 g/1 HCl and 100–150 g/1 HNO3 solution. Such conditions give outstanding results both in recovery (96.7% for Se and 99.1% for Hg) and selectivity towards lead: after cooling the solution to about 25°C, 97.5% of this metal remains in a 40% Pb residue.

Preliminary tests have shown that high purity chemical precipitates of selenium and mercury can be obtained by using a SO2 solution. When sulfur dioxide is added to selenium in a ratio of 3.3/1 (E = 670 mV SHE), Se and Hg are coprecipitated as Hg3Se2Cl2 with recoveries higher than 98%.

A careful study of the crystals’ stability shows that they can be decomposed to metallic selenium and soluble mercury chloride with a very high efficiency by keeping them under moderate oxidative conditions (900–910 mV SHE). 90% of the selenium remains in a 88% Se precipitate assaying less than 5% Hg. The mercury can thereafter be recovered by precipitation as Hg2Cl2 using iron powder as the reducing agent: with a consumption of 850 g Fe/kg Hg, the mercury yield reaches 97% and the precipitate assays 83% Hg2Cl2.

Keywords

Iron Powder Leach Liquor Mercury Removal Lead Recovery Hydrometallurgical Treatment 
These keywords were added by machine and not by the authors. This process is experimental and the keywords may be updated as the learning algorithm improves.

Preview

Unable to display preview. Download preview PDF.

Unable to display preview. Download preview PDF.

References

  1. 1.
    A. Kuivala, J. Poijarvi. Sulfuric acid washing removes mercury from roaster gases. Engineering and Mining Journal, 10, 1978, p. 81–84.Google Scholar
  2. 2.
    G. Steinveit. The Boliden-Norzink mercury removal process for purification of roaster gases. Lead Zinc Tin ′80, TMS AIME, 1980, p. 85–96.Google Scholar
  3. 3.
    T. Louderback. Selenium and the environment. Minerals Industries Bulletin, vol. 18, n° 3, 1975.Google Scholar
  4. 4.
    Amax Inc. Selenium rejection during acid leaching of matte. United States Patent, 3959097, 1976.Google Scholar
  5. 5.a
    F. Habashi. Leaching of selenides and tellurides. Principles of extractive metallurgy, vol. 2, 1970, p 52–53Google Scholar
  6. 5.b
    F. Habashi. Leaching of selenides and tellurides. Principles of extractive metallurgy, vol. 2, 1970, p 52–53 p. 139–144.Google Scholar
  7. 6.
    Inco. Process for the recovery of selenium. European patent application, 80301993.4, 1980.Google Scholar
  8. 7.
    C. Numez, F. Espiell, M. Cruells. Leaching of cinnabar with HCl-thiourea solutions as the basis of a process for mercury obtention. Metallurgical Transactions B, vol. 17B, 1986, p. 443–448.ADSGoogle Scholar
  9. 8.
    K.N. Subramanian, N.C. Nissen, A. Illis, J.A. Thomas. Recovering selenium from copper anode slimes. Society of Mining Engineers, vol. 11, 1978, p. 1538–1542.Google Scholar
  10. 9.
    H.G. Vazarlis. Hydrochloric acid-hydrogen peroxide leaching and metal recovery from a Greek zinc-lead bulk sulphide concentrate. Hydrometallurgy, n° 19, 1987, p. 243–251.Google Scholar
  11. 10.
    G. Yildirim, F.Y. Bor. Hydrometallurgical treatment of a copper refining slime rich in both selenium and tellurium. Erzmetall, n° 4, 1985, p. 196–199.Google Scholar
  12. 11.
    A. Ballester, E. Otero, F. Gonzalez. Mercury extraction from cinnabar ores using hydrobromic acid. Hydrometallurgy, n° 21, 1988, p. 127–143.Google Scholar
  13. 12.
    R.G. Holdich, G.J. Lawson. The solubility of aqueous lead chloride solutions. Hydrometallurgy, n° 19, 1987, p. 199–208.Google Scholar
  14. 13.
    A.J. Monhemius. Precipitation diagrams for metal hydroxides, sulphides, arsenates and phosphates. Transactions of the Institution of Mining and Metallurgy, vol. 86, 1977, p. C 202–206.Google Scholar
  15. 14.
    J.E. Hoffmann. Selenium and tellurium: rare but ubiquitous. Journal of the Minerals, Metals and Materials Society, vol. 41, n° 7, 1989, p. 32–48.Google Scholar
  16. 15.a
    M. Pourbaix. Atlas d’équilibres électrochimiques à 25°C. Gauthier Villars, 1963, p. 421–427;Google Scholar
  17. 15.b
    M. Pourbaix. Atlas d’équilibres électrochimiques à 25°C. Gauthier Villars, 1963,  p. 554–559.Google Scholar
  18. 16.
    L.M. Kabanova, B.V. Teplyakov. Selenium and tellurium recovery from low grade solutions by cementation on copper. The Soviet Journal of Non Ferrous Metals, vol. 5, n° 8, 1964, p. 78–79.Google Scholar
  19. 17.
    W.N. Marchant, R.O. Dannenberg, R.T. Brooks. Selenium removal from acidic waste water using zinc reduction and lime neutralization. US Bureau of Mines 1978, Report of investigations 8312.Google Scholar
  20. 18.
    P.K. Sahoo, P.C. Rath. Recovery of lead from complex leach residue by cementation with iron. Hydrometallurgy, n° 20, 1988, p. 169–177.Google Scholar

Copyright information

© Institution of Mining and Metallurgy 1991

Authors and Affiliations

  • D. D’Hondt
    • 1
  • N. Gérain
    • 1
  • A. Van Lierde
    • 1
  1. 1.Unité des ProcédésUniversité Catholique de LouvainLouvain-La-NeuveBelgium

Personalised recommendations