Speciation of Co(II) and Ni(II) in anaerobic bioreactors measured by competitive ligand exchange-adsorptive stripping voltammetry.

Competitive ligand exchange-adsorptive stripping voltammetry is applied to speciation analysis of dissolved Ni(II) and Co(II) in an anaerobic bioreactor and similar batch media. Co and Ni speciation in these media can be measured down to concentration levels of ca. 1 nM. Sulfide interference is avoided via removal as H2S. In methanogenic bioreactors, up to 95% of the dissolved Co and Ni is present in strongly bound forms, with complex stabilities > or =10(8)-10(9) and 10(7)-10(8) mol(-1) L, respectively. In effluent from sulfate-reducing bioreactors, Co is also found to be present in a strongly bound form, and up to micromolar levels of strongly complexing excess ligand was detected. The predominant presence of Co and Ni in strong complexes, with concomitant low free dissolved concentrations, is significant for limitation by these elements in anaerobic bioreactors.

Faradaic depolarization in the electrokinetics of the metal-electrolyte solution interface.

Streaming potentials (E(str)) have been measured in a flat thin-layer cell with gold and aluminum surfaces. The conventional relation between E(str) and the zeta-potential is shown to be applicable only as long as charge transfer reactions at the metal-electrolyte solution interface are insignificant in terms of the ensuing contribution to the overall cell conductivity. Owing to the irreversibility of the reduction/oxidation of water at most metal surfaces, streaming potentials can be obtained over a very broad range of pressure gradients for metallic substrates in electrolytes such as KNO3. The situation changes drastically in the presence of a reversible redox couple like Fe(CN)(6)3-/Fe(CN)(6)4-. Even small streaming potentials are then greatly diminished due to the extensive conduction that results from the bipolar electrolysis at the metal surface. For gold and aluminum in the presence of various electroinactive and electroactive electrolytes, the measured values for E(str) are shown to be consistent with their conventional voltammetric characteristics.