HEAVY-METALS IN THE ENVIRONMENT - TRACE-METAL SOLUBILITY IN SOILS ANDWATERS RECEIVING DEICING SALTS

Citation
C. Amrhein et al., HEAVY-METALS IN THE ENVIRONMENT - TRACE-METAL SOLUBILITY IN SOILS ANDWATERS RECEIVING DEICING SALTS, Journal of environmental quality, 23(2), 1994, pp. 219-227
Citations number
16
Categorie Soggetti
Environmental Sciences
ISSN journal
00472425
Volume
23
Issue
2
Year of publication
1994
Pages
219 - 227
Database
ISI
SICI code
0047-2425(1994)23:2<219:HITE-T>2.0.ZU;2-D
Abstract
Laboratory batch incubation studies were carried out to determine the effects of aerobic and anaerobic conditions on the solubility of trace metals in soils and waters treated with the deicing salts calcium mag nesium acetate (CMA) and NaCl. The concentrations of trace metals were , in general, not controlled by equilibrium reactions but rather by th e relative rates of several simultaneous and sequential reactions. In three soils from CA, NJ, and MI, and water treated with CMA the produc tion of HCO3 from acetate decomposition initially increased the soluti on concentration of Pb and Zn as PbCO30 and ZnCO30 . Eventually, super saturation with respect to calcite occurred and the concentrations of Cu, Cd, Zn, V, and Cr decreased because of coprecipitation with the ca lcite. The precipitation of pyromorphite [Pb-5(PO4)Cl] was suspected b ased on elevated saturation indexes for this mineral. At low redox con ditions, the solubilization of Fe- and Mn-oxides increased the concent ration of the trace metals that were adsorbed or coprecipitated with t hese phases. Supersaturation with respect to MnCO3, FeCO3, and VO(OH)( 2) occurred under low redox conditions. The rate constant for acetate decomposition under anaerobic conditions was 18 times lower than the r ate constant for aerobic decomposition. This suggests that if a soil r eceived a high loading of CMA, low Ct conditions could occur and CMA m ight leach to groundwater. There is evidence that the use of CMA could result in Pb and Zn mobilization as neutral ion pairs with carbonate.