Manganese oxides have been recently
investigated as excellent catalysts
for peroxymonosulfate (PMS) activation, and the reported mechanisms
are mostly forming reactive oxygen species (ROSs). This study investigated
the use of iron-doped manganese oxide, synthesized via air oxidation
under strong alkaline conditions. The oxidation of three substrates
was affected by their adsorption at the catalyst surface, solution
pH, and co-solutes. Common ROS scavengers inhibited the oxidation
of bisphenol A (BPA), suggesting the possible involvement of ROSs;
however, the PMS decomposition tests with and without BPA and the
comparison with a 1O2-generation system ruled
out the formation of ROSs and pointed to direct electron transfer
between the adsorbed BPA and complexed PMS as the mechanism. To prove
this mechanism, the catalyst was coated to graphite sheets and a galvanic
oxidation process (GOP) was developed to separate BPA and PMS into
two half cells. Upon PMS addition into one cell, BPA was quickly oxidized
in the other cell, confirming the occurrence of electron transfer.
The GOP system successfully degraded BPA in both surface water and
hypersaline shale gas-produced water. Overall, this study developed
a new catalyst for PMS activation and unveiled the advantages and
potential applications of electron shuttling catalysts.