•TiO2 nanotubes were grown on a PbO2-based anode to produce a larger band gap that favors HO radical production, destroys ofloxacin and presents lower energy consumption.•The ofloxacin electrodegradation pathway was analyzed.•The mass transfer impact to electrochemical oxidation efficiency was analyzed using a differential column batch reactor.Electrochemical oxidation has been proposed for the destruction of organic contaminants; however, this process is hampered by low oxidation efficiency and high energy cost. Accordingly, we developed a TiO2-based SnO2-Sb/polytetrafluroethylene resin (FR)-PbO2 electrode that was based on TiO2 nanotubes. We tested the performance of the electrode on an antibiotic, ofloxacin, and identified the major pathway of ofloxacin oxidation. We found growing TiO2 nanotubes on Ti material increased current efficiency, and the electrical efficiency per order (EE/O, kWh/m3) for oxidation was decreased by 16.2%. Our electrode requires a large overpotential before electrons flow, which minimizes oxygen evolution, reduces hydrogen peroxide and ozone generation, and favors hydroxyl radicals (HO) production. We found the electron efficiency (EE) during oxidation was as high as 88.45%. In other words, 88.45% of the electrons that flow out of the electrode cause oxidation. The effects of current density, initial concentration, pH value and electrolyte concentration were investigated. A differential column batch reactor (DCBR) was used to simulate the performance of continuous plug flow reactor and we found that the destruction of ofloxacin followed pseudo-first order model. We also evaluated the impact of mass transfer on electrochemical performance. The effects of fluid velocity and electrode spacing on oxidation rate were evaluated by determining the mass transfer coefficient and the effectiveness factor Ω (between 0 and 1). Our experiments and calculations indicated that the mass transfer reduced oxidation rate by more than 55% (Ω < 0.45) for an electrode spacing of 1 cm at a fluid velocity of 0.033 m/s. Unlike studies carried out using completely mixed batch reactor, the DCBR can simulate the flow conditions in pilot or full scale reactors; consequently, observed pseudo-first order rate constants in the DCBR can be used for preliminary design.Download high-res image (170KB)Download full-size image

•Pollenkitt is a viscous coating on many pollen grains.•Pollen absorbs moisture; uptake is greater for grains with pollenkitt.•Adhesion of sunflower pollen to surfaces was measured as a function of humidity.•Pollenkitt gives pollen the ability to tune adhesion with changes in humidity.Pollens possess a thin liquid coating, pollenkitt, which plays a major role in adhesion by forming capillary menisci at interfaces. Unfortunately, the influence of humidity on pollenkitt properties and capillary adhesion is unknown. Because humidity varies widely in the environment, the answers have important implications for better understanding plant reproduction, allergy and asthma, and pollen as atmospheric condensation nuclei. Here, pollenkitt-mediated adhesion of sunflower pollen to hydrophilic and hydrophobic surfaces was measured as a function of humidity. The results quantify for the first time the significant water absorption of pollenkitt and the resulting complex dependence of adhesion on humidity. On hydrophilic Si, adhesion increased with increasing RH for pollens with or without pollenkitt, up to 200 nN at 70% RH. In contrast, on hydrophobic PS, adhesion of pollenkitt-free pollen is independent of RH. Surprisingly, when pollenkitt was present adhesion forces on hydrophobic PS first increased with RH up to a maximum value at 35% RH (∼160 nN), and then decreased with further increases in RH. Independent measurement of pollenkitt properties is used with models of capillary adhesion to show that humidity-dependent changes in pollenkitt wetting and viscosity are responsible for this complex adhesion behavior.