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Stability constants for metal arsenates

Janice S. Lee A B C and Jerome O. Nriagu A

A Department of Environmental Health Sciences, School of Public Health, University of Michigan, Ann Arbor, MI 48109, USA.
B Present address: National Health and Environmental Effects Laboratory, US Environmental Protection Agency, Research Triangle Park, NC 27711, USA.
C Corresponding author. Email: Lee.JaniceS@epa.gov

Environmental context. The behaviour of arsenic compounds is controlled by their solubility, which in turn controls both the forms and mobility of arsenic in the environment. Current knowledge on arsenic chemistry may be distorted because information available on the solubility of arsenic compounds usually does not include possible formation of metal–arsenate complexes. Our results show the formation of stable metal–arsenate complexes that have not been considered before, and this new data can be used to further examine the effect of these complexes on controlling the fate and transport of arsenic in the environment.

Abstract. The formation of solid metal arsenates could conceivably reduce the concentrations of arsenate and metal ions in natural and contaminated aqueous ecosystems, and possibly in human body fluids. In this study, solid metal arsenates were dissolved isothermally in solutions with different molar concentrations of arsenic acid. The saturated solutions were analysed and the results processed to derive the solubility products (Ksp) for solid phases and association constants (K) for metal arsenate ion-pairs. Ion chromatography was used to confirm the presence of ion-pairs, some of which had never before been considered. Association constants were determined for the following ion-pairs: FeHAsO4+ (log K = 4.88), CoHAsO40 (log K = 1.50), ZnHAsO40 (log K = 3.28), SrH2AsO4+ (log K = 1.72), and Ag2H2AsO4+ (log K = 4.50). The following metal ions apparently do not form stable complexes with HAsO42–: Cd2+, Cr3+, Cu2+, Mg2+, Mn2+, Ni2+, Pb2+, and Sn2+. Standard state solubility products (Ksp°) were redetermined for the following compounds: Ag3AsO4, Cd3(AsO4)2, Co3(AsO4)2, CrAsO4, Cu3(AsO4)2, FeAsO4, Mg3(AsO4)2, MnHAsO4, NiHAsO4, PbHAsO4, Sn3(AsO4)2, Sr3(AsO4)2, Zn3(AsO4)2·Zn3(AsO4)2·8H2O (koettigite), Cu2Al7(AsO4)4(OH)13·12H2O (ceruleite), and Pb2CuAsO4CrO4OH (fornacite). Our results show the formation of ion-pairs for some metal arsenates and indicate that previous studies have overestimated the solubilities of many arsenates.

Environmental Chemistry 4(2) 123–133    doi:10.1071/EN06070
Submitted: 15 November 2006    Accepted: 15 March 2007    Published: 17 April 2007





   
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