Photolysis of ferric ions in the presence of sulfate or chloride ions: implications for the photo-Fenton process.

The photo-Fenton process (Fe(2+)/Fe(3+), H(2)O(2), UV light) is one of the most efficient and advanced oxidation processes for the mineralization of the organic pollutants of industrial effluents and wastewater. The overall rate of the photo-Fenton process is controlled by the rate of the photolytic step that converts Fe(3+) back to Fe(2+). In this paper, the effect of sulfate or chloride ions on the net yield of Fe(2+) during the photolysis of Fe(3+) has been investigated in aqueous solution at pH 3.

Abatement of the inhibitory effect of chloride anions on the photo-Fenton process.

The inhibition of the photo-Fenton (Fe2+/Fe3+, H2O2, UV light) degradation of synthetic phenol wastewater solutions by chloride ions is shown to affect primarily the photochemical step of the process, having only a slight effect on the thermal or Fenton step. Kinetic studies of the reactions of oxoiron (IV) (FeO2+) with phenol indicate that, if FeO2+ is formed in the photo-Fenton degradation, its role is probably minor. Finally, it is shown that, for both a synthetic phenol wastewater and an aqueous extract of Brazilian gasoline, the inhibition of the photo-Fenton degradation of the organic material in the presence of chloride ion can be circumvented by maintaining the pH of the medium at or slightly above 3 throughout the process, even in the presence of significant amounts of added chloride ion (0.

Laser flash photolysis and time-resolved fluorescence measurements of the aggregation number of SDS-biopolymer complexes.

Aqueous solutions of 0.5% sodium carboxymethyl cellulose, NaCMC, and 2-hydroxyethyl cellulose, HEC, and variable concentration of sodium dodecyl sulfate, SDS, were studied by the intensities ratio of pyrene fluorescence bands (I/III and monomer/excimer) and conductance measurements to determine the critical aggregation concentration, cac, and the degree of micellar dissociation, alpha, respectively. The cac of these systems is close to 2-4 x 10(-3)M and values of alpha are consistent with the formation of SDS micelles adsorbed cooperatively to the polymer backbone.