Nanosecond transient absorption studies of the pH-dependent hydrated electron quenching by HSO3.

ABSTRACT

The large standard reduction potential of an aqueous solvated electron (eaq-, E° = -2.9 V) makes it an attractive candidate for reductive treatment of wastewater contaminants. Using transient absorption spectroscopy, the nanosecond to microsecond dynamics of eaq- generated from 10 mM solutions of Na2SO3 at pH 4 to 11 in H2O and D2O are characterized, resulting in the determination that between pH 4 and 9 it is the HSO3-, and not H+ as previously postulated by others, that effectively quenches eaq-. The observed bimolecular quenching rate constant (k = 1.2 × 108 M-1 s-1) for eaq- deactivation by HSO3- is found to be consistent with a Brønsted acid catalysis mechanism resulting in formation of H˙ and SO32-. A large solvent isotope effect is observed from the lifetimes of the eaq- in H2O compared to D2O (kH2O/kD2O = 4.4). In addition, the bimolecular rate constant for eaq- deactivation by DSO3- (k = 2.7 × 107 M-1 s-1) is found to be an order of magnitude lower than by HSO3-. These results highlight the role of acids, such as HSO3-, in competition with organic contaminant targets for eaq- and, by extension, that knowledge of the pKa of eaq- sources can be a predictive measure of the effective pH range for the treatment of wastewater contaminants.