We present a numerical model of a surface microdischarge (SMD) in humid air at atmospheric pressure. Our model includes over 50 species and 600 elementary reactions and consists of two, coupled well-mixed regions: a discharge layer with both charged and neutral species and an afterglow region consisting only of neutral species. Multiple time steps employed in our model enable capturing rapid dynamic behaviour in the discharge layer as well as the relatively slow diffusion and reaction in the afterglow. A short duration, high electric field is assumed to be excited at 10 kHz in the discharge region with power density maintained at 0.05 W cm−2. Among the predicted dominant species in the afterglow are O3, N2O5, N2O, HNO3, H2, NO3, H2O2, HNO2 and NO2. The results are in qualitative agreement with Fourier transform infrared absorption spectroscopy. Our simulation results show that density of those reactive species continues to evolve significantly in time, even after ∼15 min of SMD exposure. This result suggests that SMD treatments on the order of minutes or less may involve significant neutral species concentration and flux transients, potentially affecting interpretation of results.

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Indirect air dielectric barrier discharge in close proximity to water creates an acidified, nitrogen-oxide containing solution known as plasma-activated water (PAW), which remains antibacterial for several days. Suspensions of E. coli were exposed to PAW for either 15 min or 3 h over a 7-day period after PAW generation. Both exposure times yielded initial antibacterial activity corresponding to a ∼5-log reduction in cell viability, which decreased at differing rates over 7 days to negligible activity and a 2.4-log reduction for 15 min and 3 h exposures, respectively. The solution remained at pH ∼2.7 for this period and initially included hydrogen peroxide, nitrate and nitrite anions. The solution composition varied significantly over this time, with hydrogen peroxide and nitrite diminishing within a few days, during which the antibacterial efficacy of 15 min exposures decreased significantly, while that of 3 h exposures produced a 5-log reduction or more. These results highlight the complexity of PAW solutions where multiple chemical components exert varying biological effects on differing time scales.

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We present the transient, dynamic behavior of ozone production in surface micro-discharge (SMD) plasma in ambient air. Ultraviolet absorption spectroscopy at 254 nm was used to measure the time development of ozone density in a confined volume. We observed that ozone density increases monotonically over 1000 ppm for at least a few minutes when the input power is lower than ∼0.1 W/cm 2 . Interestingly, when input power is higher than ∼0.1 W/cm 2 , ozone density starts to decrease in a few tens of seconds at a constant power density, showing a peak ozone density. A model calculation suggests that the ozone depletion at higher power density is caused by quenching reactions with nitrogen oxides that are in turn created by vibrationally excited nitrogen molecules reacting with O atoms. The observed mode transition is significantly different from classical ozone reactors in that the transition takes place over time at a constant power. In addition, we observed a positive correlation between time-averaged ozone density and the inactivation rate of Escherichia coli on adjacent agar plates, suggesting that ozone plays a key role in inactivating bacteria under the conditions considered here.