Speciation 98: Abstracts
Staffan Sjöberg
Department of Inorganic Chemistry, Umeå University, Sweden
Biota like bacteria and algae are ubiquitous in natural waters and their cell walls show a strong affinity for a wide variety of metal cations. This is understandable thinking of the variety of surface functional groups of these cell walls, including amino, carboxylic, hydroxyl, thio and phosphate sites.
In order to be able to interpret toxicity, bioavailability, transport and deposition of trace metals a more detailed understanding of the different uptake processes is required.
Recently, some results have been published (1,2,3) showing how the adsorption of metal ions to algal and bacterial surfaces can be described by chemical equilibrium models similar to those for hydrous mineral surfaces. The customary way to represent reactions at these surfaces has been through equilibria of the type:
=SOH + Me2+ ![]() | (1) |
=SOH + Me2+ ![]() | (2) |
2=SOH + Me2+ ![]() | (3) |
The degree of protonation depends on the acid-base
equilibria
=SOH + H+ ![]() | (4) |
=SOH ![]() | (5) |
Equilibria (1) to (5) can be described by charge dependent stability constants according to the "surface complexation" concept.
Different models for metal adsorption onto surfaces of algae and bacteria will be presented and discussed.
References