Boron-doped diamond (BDD) electrodes have the greatest known oxygen overpotential range; a characteristic that has allowed the material to be well suited for electro-oxidation processes in aqueous media.
The efficacy of electrocoagulation at a pilot-scale as an alternative drinking water treatment technology to conventional coagulation is explored. A novel reactor was integrated into a pilot plant at the surface water supply of a small, remote community. Using iron anodes, the effect of metal loading (ML), current density and inter-electrode gap on the reduction of natural organic matter (NOM) was studied. Dissolved organics were characterized by large fractions of low molecular weight (<750 Da) hydrophilic carbon structures with lower charge density. A greater reduction in UV254 was yielded compared to dissolved organic carbon, indicating better removal of larger molecular weight fractions of NOM. As ML dosages increased from 27.8 to 60.8 mg/L, specific ultraviolet absorbance decreased from 1.92 ± 0.14 to 1.60 ± 0.10 L/m•mg respectively, from an initial raw water value of 2.21 L/m•mg. No clear trend was observed for the effect of current density and inter-electrode gap for NOM, however ML was the primary variable dictating the process' effectiveness. Energy requirements were observed to vary greatly and were highly dependent on ML, current density and inter-electrode gap; variables that all effect the operating potential and resistance. In general, conditions that yielded the greatest reduction of NOM, a 1 mm gap and 4-cell configuration, had energy requirements between 0.480 and 0.602 kWh/m of water treated.
Difficulties arise related to the economy-of-scale and practicability in applying conventional water treatment technologies to small and remote systems. A promising oxidation technology better suited for these applications is that of electro-oxidation (EO), whereby contaminants are degraded via direct, advanced, and/or electrosynthesized oxidant-mediated reactions. One species of oxidants of particular interest includes ferrates (Fe(VI)/(V)/ (IV)), where only recently has their circumneutral synthesis been demonstrated, using high oxygen overpotential (HOP) electrodes, namely boron-doped diamond (BDD). In this study, the generation of ferrates using various HOP electrodes (BDD, NAT/Ni−Sb− SnO 2 , and AT/Sb-SnO 2 ) was investigated. Ferrate synthesis was pursued in a current density range of 5−15 mA cm −2 and initial Fe 3+ concentrations of 10−15 mM. Faradaic efficiencies ranged from 11−23%, depending on operating conditions, with BDD and NAT significantly outperforming AT electrodes. Speciation tests revealed that NAT synthesizes both ferrate(IV/V) and ferrate(VI), while the BDD and AT electrodes synthesized only ferrate(IV/V) species. A number of organic scavenger probes were used to test the relative reactivity, including nitrobenzene, carbamazepine, and fluconazole, whereby ferrate(IV/V) was significantly more oxidative than ferrate(VI). Finally, the ferrate(VI) synthesis mechanism by NAT electrolysis was elucidated, where coproduction of ozone was found to be a key phenomenon for Fe 3+ oxidation to ferrate(VI).
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