The complex composition of natural organic matter (NOM) can affect drinking water treatment processes, leading to perceptible and undesired taste, color and odor, and bacterial growth. Further, current treatments tackling NOM can generate carcinogenic by-products. In contrast, promising substitutes such as electrochemical methods including electrooxidation (EO) have shown safer humic acid and algae degradation, but a formal comparison between EO methods has been lacking. In this study, we compared the Boron-doped diamond (BDD) electrode electrolysis performance for Suwannee River NOM degradation using mixed-metal oxide (MMO) anodes under different pH (6.5 and 8.5) representative of the high and low ranges for acidity and alkalinity in wastewater and applied two different current densities (10 and 20 mA cm⁻²). BDD anodes were combined with either BDD cathodes or stainless steel (SS) cathodes. To characterize NOM, we used (a) total organic compound (TOC), (b) chemical oxygen demand (COD), (c) specific ultraviolet absorbance (SUVA), and (d) specific energy consumption. We observed that NOM degradation differed upon operative parameters on these two electrodes. BDD electrodes performed better than MMO under stronger current density and higher pH and proved to be more cost-effective. BDD-SS electrodes showed the lowest energy consumption at 4.4 × 10³ kWh kg COD⁻¹. while obtaining a TOC removal of 40.2%, COD of 75.4% and SUVA of 3.4 at higher pH and current. On the contrary, MMO produced lower TOC, COD and SUVA at the lower pH. BDD electrodes can be used in surface water as a pre-treatment in combination with some other purification technologies to remove organic contaminants.

The persistence of pharmaceuticals and personal care products (PPCPs) in water has been a cause for concern for several years. Many studies have successfully used TiO₂/UV photocatalysis to remove these compounds from water. In order to optimize these systems for large-scale water treatment, the effects of the reaction matrix, methods to improve energy efficiency, and methods for easy catalyst separation must be considered. The following study examines the photocatalytic degradation of a cocktail of 18 PPCPs using a porous titanium–titanium dioxide membrane and the effect of solution pH on kinetic rate constants. The addition of methanol to the reaction—commonly used as a carrier solvent—had a significant effect on kinetic rate constants even at low concentrations. Solution pH was also found to influence kinetic rate constants. Compounds had higher kinetic rate constants when they were oppositely charged to the membrane at experimental pH as opposed to similarly charged, suggesting that electrostatic forces have a significant effect. The controlled periodic illumination of UV–LEDs was also investigated to increase photonic efficiency. The dual-frequency light cycle used did not cause a decrease in degradation for many compounds, successfully increasing the photonic efficiency without sacrificing performance.