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Research article2009Peer reviewed

Nucleation and crystallization of otavite, witherite, calcite, strontianite, hydrozincite, and hydrocerussite by CO2 membrane diffusion technique

Bucca, Maurizio; Dietzel, Martin; Tang, Jianwu; Leis, Albrecht; Koehler, Stephan Juergen

Abstract

Otavite, witherite, calcite, strontianite. hydrozincite and hydrocerussite nucleation was induced by CO2 diffusion through a polyethylene membrane into a metal bearing solution. Nucleation and ongoing precipitation was followed at 25 +/- 1 degrees C by the chemical evolution of the solution and the consumption of sodium hydroxide (pH-slat conditions). X-ray diffraction patterns as well as FT infrared and Raman spectra confirmed the formation of well crystallized solids, except for less crystalline hydrozincite. In several experiments simonkolleite and laurionite precipitated concurrently with hydrozincite and hydrocerussite. The carbonate end-member minerals, smithsonite and cerussite, however were not formed. Carbonate minerals crystallized as spherical aggregates of thin layered otavite, spherical orientated witherite needles, rhombohedral calcite, pseudo-hexagonal strontianite laths, fibrous lumps of hydrozincite and planar hexagonal hydrocerussite crystals. Crystal and aggregate sizes range between 1 and 100 mu m. Nucleation occurred at well defined reaction times and distinct critical supersaturation indices (SIcrit). The time for nucleation at constant pH decreased as the initial metal concentration increased for a given solid. The SIcrit values decreased in the order of hydrocerussite (3.2), otavite (2.5), strontianite (1.6), witherite (0.9) and calcite (0.7). (C) 2009 Elsevier B.V. All rights reserved.

Keywords

Heavy metals; Carbonates; Nucleation; Hydroxides; CO2 diffusion

Published in

Chemical Geology
2009, Volume: 266, number: 3-4, pages: 143-156
Publisher: ELSEVIER SCIENCE BV

    UKÄ Subject classification

    Geosciences, Multidisciplinary

    Publication identifier

    DOI: https://doi.org/10.1016/j.chemgeo.2009.06.002

    Permanent link to this page (URI)

    https://res.slu.se/id/publ/89828