SUSPENDED PARTICULATE OXIDES AND ORGANIC-MATTER INTERACTIONS IN TRACE-METAL SORPTION REACTIONS IN A SMALL URBAN RIVER

Citation
La. Warren et Ap. Zimmerman, SUSPENDED PARTICULATE OXIDES AND ORGANIC-MATTER INTERACTIONS IN TRACE-METAL SORPTION REACTIONS IN A SMALL URBAN RIVER, Biogeochemistry, 24(1), 1994, pp. 21-34
Citations number
49
Categorie Soggetti
Environmental Sciences","Geosciences, Interdisciplinary
Journal title
ISSN journal
01682563
Volume
24
Issue
1
Year of publication
1994
Pages
21 - 34
Database
ISI
SICI code
0168-2563(1994)24:1<21:SPOAOI>2.0.ZU;2-Z
Abstract
The relative scavenging abilities of suspended particulate oxides (SPO X), and organic matter (SPOM) for Cd, Zn and Cu were evaluated in a sm all, anthropogenically influenced river. In addition, the factor most important in influencing the sorption density (A(d): metal concentrati on associated with a given phase divided by the concentration of that geochemical phase in the suspended particulate pool) of each metal to SPOX and SPOM were identified through multiple linear regression analy ses from the suite of: pH, temperature, dissolved metal concentration, and the concentration of the other particulate fraction. Results indi cate that SPOX-SPOM interactions do occur in trace metal complexation reactions; and interactions are both phase and cation specific. Fe oxi des are able to outcompete discrete organic binding sites for Cu and Z n as a relative decrease in the amount of these two cations sorbed to organic matter was observed with increasing particulate Fe oxides. SPO M concentration was identified as being most important in influencing Cu sorption densities associated with the SPOX fraction. Organic matte r - oxide complexes are postulated to occur that enhance oxide sorptio n of Cu such that relatively more Cu is sorbed to particulate oxides w ith increasing particulate organic matter concentrations. Dissolved co ncentrations of Cd and Zn were found to be most important in influenci ng the sorption densities for these two metals associated with the oxi des fraction. The sorption behaviour appears to follow Freundlich isot herm behaviour where the amount sorbed is a function of the dissolved concentration.