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Solubility and surface spectroscopy of zinc precipitates on calcite

Journal Article · · Geochimica et Cosmochimica Acta; (USA)
;  [1]; ;  [2]
  1. Pacific Northwest Lab., Richland, WA (USA)
  2. Washington State Univ., Pullman (USA)

The sorption and precipitation of Zn was investigated in equilibrium calcite (CaCO{sub 3(S)}) suspensions at Zn concentrations that approached and exceed the solubility of known zinc carbonate solids. Surface-enhanced precipitation was not observed and CaCO{sub 3(S)} did not nucleate Zn solids when the aqueous ion activity product (IAP) was below the equilibrium IAP of the least soluble, kinetically viable Zn phase. The CaCO{sub 3(S)} surface was not requisite for Zn precipitation. When CaCO{sub 3(S)} was present the precipitate formed a surface coating or discrete Zn particles bound to the surface. X-ray photoelectron spectroscopy, X-ray diffraction, and energy dispersive X-ray spectrometry of both Zn-treated CaCO{sub 3(S)} and isolated Zn particles implied, but did not confirm, that the precipitate was hydrozincite or its hydrated form. Zinc-treated calcite maintained Zn concentrations that agreed with the solubility of a synthetic hydrozincite measured by Schindler et al (1969). Direct measurements showed that the equilibrium solubility of the precipitate exceeded that of a natural hydrozincite and was less than a natural smithsonite (log IAP = a{sub Zn{sup 2+}}a{sub CO{sub 3}{sup 2{minus}}} = {minus}10.53 {plus minus} 0.10). It is suggested that a poorly ordered form of hydrozincite that regulates Zn activities at higher levels than well-crystallized natural varieties readily precipitates in CaCO{sub 3(aq)}/CaCO{sub 3(S)} systems. The environmental significance of this phase is unknown.

OSTI ID:
7145094
Journal Information:
Geochimica et Cosmochimica Acta; (USA), Journal Name: Geochimica et Cosmochimica Acta; (USA) Vol. 53:1; ISSN GCACA; ISSN 0016-7037
Country of Publication:
United States
Language:
English

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