Oxidation mechanisms of CF2Br2 and CH2Br2 induced by air nonthermal plasma.

Oxidation mechanisms in air nonthermal plasma (NTP) at room temperature and atmospheric pressure were investigated in a corona reactor energized by +dc, -dc, or +pulsed high voltage.. The two bromomethanes CF(2)Br(2) and CH(2)Br(2) were chosen as model organic pollutants because of their very different reactivities with OH radicals. Thus, they served as useful mechanistic probes: they respond differently to the presence of humidity in the air and give different products. By FT-IR analysis of the postdischarge gas the following products were detected and quantified: CO(2) and CO in the case of CH(2)Br(2), CO(2) and F(2)C ═ O in the case of CF(2)Br(2). F(2)C ═ O is a long-lived oxidation intermediate due to its low reactivity with atmospheric radicals. It is however removed from the NTP processed gas by passage through a water scrubber resulting in hydrolysis to CO(2) and HF. Other noncarbon containing products of the discharge were also monitored by FT-IR analysis, including HNO(3) and N(2)O. Ozone, an important product of air NTP, was never detected in experiments with CF(2)Br(2) and CH(2)Br(2) because of the highly efficient ozone depleting cycles catalyzed by BrOx species formed from the bromomethanes. It is concluded that, regardless of the type of corona applied, CF(2)Br(2) reacts in air NTP via a common intermediate, the CF(2)Br radical. The possible reactions leading to this radical are discussed, including, for -dc activation, charge exchange with O(2)(-), a species detected by APCI mass spectrometry.

Comparison of the rates of phenol advanced oxidation in deionized and tap water within a dielectric barrier discharge reactor.

Electric non-thermalizing discharges provide promising novel means to induce oxidation of organic pollutants in water. The decomposition of phenol in solutions prepared with deionized (milliQ) and tap water was studied and compared in a Dielectric Barrier Discharge (DBD) reactor. Interestingly, a significant rate increase was found in tap with respect to milliQ water. Control experiments proved that this was not the effect of conductivity or of traces of iron or of residual active chlorine from the depuration process operated in the aqueducts of Italian cities. The same increase in efficiency as observed in tap water was instead obtained when phenol was treated in solutions containing bicarbonate anions in the same concentration as present in tap water, an effect attributed to buffering of the solution pH. The role of pH has been investigated thoroughly by measuring the process efficiency over a wide pH range, from 2 to 10, by using different buffer systems to probe reactivity at near neutral pH, the most relevant for drinking water applications, and by testing the effect of different buffer concentrations. These latter experiments failed to detect any significant kinetic effect attributable to the well known reactivity of bicarbonate as quencher of OH radicals.

Comparison of toluene removal in air at atmospheric conditions by different corona discharges.

Different types of corona discharges, produced by DC of either polarity (+/-DC) and positive pulsed (+pulsed) high voltages, were applied to the removal of toluene via oxidation in air at room temperature and atmospheric pressure. Mechanistic insight was obtained through comparison of the three different corona regimes with regard to process efficiency, products, response to the presence of humidity and, for DC coronas, current/voltage characteristics coupled with ion analysis. Process efficiency increases in the order +DC < -DC < +pulsed, with pulsed processing being remarkably efficient compared to recently reported data for related systems. With -DC, high toluene conversion and product selectivity were achieved, CO(2) and CO accounting for about 90% of all reacted carbon. Ion analysis, performed by APCI-MS (Atmospheric Pressure Chemical Ionization-Mass Spectrometry), provides a powerful rationale for interpreting current/voltage characteristics of DC coronas. All experimental findings are consistent with the proposal that in the case of +DC corona toluene oxidation is initiated by reactions with ions (O(2)(+*), H(3)O(+) and their hydrates, NO(+)) both in dry as well as in humid air. In contrast, with -DC no evidence is found for any significant reaction of toluene with negative ions. It is also concluded that in humid air OH radicals are involved in the initial stage of toluene oxidation induced both by -DC and +pulsed corona.