Abstract
The photooxidation of water by aqueous cerium(IV) has been investigated in dilute sulfuric acid quantitatively using a diode array spectrophotometer. An overview of experimental data on the speciation of cerium(IV) showed that several different absorbing species are present under almost all conditions, which makes straightforward interpretation of photochemical data very difficult. At submillimolar levels of cerium(IV) in 0.10 mol dm–3 sulfuric acid, a consistent quantum yield of 0.12 for the loss of cerium(IV) could be determined, but even under these conditions, clear evidence of a parallel non-photochemical pathway was obtained. At higher concentrations of the metal ion, significant deviations from the expected direct proportionality between the illumination ratio and the initial rate were confirmed, which can only be interpreted by a complicated system of parallel, coupled photochemical and non-photochemical pathways. The inhibitory effect of aqueous cerium(III) in the process was also demonstrated. Based on indirect evidence, it seems likely that sulfate ion radicals play a significant role in the mechanism.
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