Search

Dielectric barrier discharges are an emerging technology for the plasma-catalytic removal of volatile organic compounds and other gas purification challenges such as the removal of O2 traces from H2. Packed-bed reactors are mainly used for these applications, but surface dielectric barrier discharges (SDBDs) typically printed on thin dielectric plates are promising alternatives for the treatment of large volumetric flow rates due to their low flow resistance causing a low pressure drop. Especially for SDBDs the flow conditions are crucial, because the active plasma filled volume covering the mentioned plates with a typical thickness of 0.1 mm is small in comparison to the overall reactor volume with a typical distance of some tens of millimeters to the reactor wall. In this study, the flow conditions of a twin-SDBD were investigated by Schlieren imaging applied in converting O2 traces in H2 containing gas mixtures to H2O and compared to fluid dynamics simulations. Schlieren imaging was used to visualize local gradients of the refractive index inside the SDBD reaction chamber, while gas composition, dissipated power, or flow rate were varied. Without a plasma discharge, laminar flow dominates, resulting in a conversion below 10% over a Pt-coated electrode configuration in the reaction of O2 traces with H2. With the plasma discharge, full conversion was achieved for the same reaction without catalyst, although the plasma is also confined to the surface of the electrode configuration. Schlieren structures covering the complete cross section of the reaction chamber were observed, showing that strong radial mass transport is induced by the plasma. The shape and extent of the Schlieren structures is ascribed to a superimposition of gas flow, thermal expansion from the plasma volume, thermal buoyancy as well as an electrohydrodynamic force between the electrodes and the grounded reactor walls. Fluid dynamics simulations show vortex formation above and below the electrode, created by the electrohydrodynamic force further implying extensive mass transport by the plasma, which is visualized in addition by carbonaceous deposits on the reactor lid. This emerging deposition pattern during toluene decomposition closely corresponds to the electrode geometry. It is proposed that the reaction proceeds only in the active plasma volume and that reactive species transported to the bulk gas phase only have a minor contribution. Thus, the degree of conversion of the SDBD reactor is not only determined by the chemical reactivity in the plasma volume, but also by its plasma-induced mass transport resulting in efficient gas mixing. These findings reveal new possibilities to improve SDBD reactors for gas purification applications based on their favorable flow conditions. [ABSTRACT FROM AUTHOR]

A twin surface dielectric barrier discharge is used for the catalyst‐enhanced plasma oxidation of 300 ppm n‐butane in synthetic air. Plasma‐only operation results in the conversion of n‐butane into CO and CO2. Conversion is improved by increasing the temperature of the feed gas, but selectivity shifts to undesired CO. α‐MnO2 is used as a catalyst deposited on the electrodes by spray coating with a distance of 1.5 mm between the uncoated grid lines and the square catalyst patches to prevent the inhibition of plasma ignition. The catalyst strongly influences selectivity, reaching 40% conversion and 73% selectivity to CO2 at a specific energy density of 390 J·L−1 and 140°C, which is far below the onset temperature of thermocatalytic n‐butane conversion. [ABSTRACT FROM AUTHOR]

A volume and a twin surface dielectric barrier discharge (VDBD and SDBD) are generated in different nitrogen–oxygen mixtures at atmospheric pressure by applying damped sinusoidal voltage waveforms with oscillation periods in the microsecond time scale. Both electrode configurations are located inside vacuum vessels and operated in a controlled atmosphere to exclude the influence of surrounding air. The discharges are characterised with different spatial and temporal resolution by applying absolutely calibrated optical emission spectroscopy in conjunction with numerical simulations and current–voltage measurements. Plasma parameters, namely the electron density and the reduced electric field, and the dissipated power are found to depend strongly on the oxygen content in the working gas mixture. Different spatial and temporal distributions of plasma parameters and dissipated power are explained by surface and residual volume charges for different O2 admixtures due to their effects on the electron recombination rate. Thus, the oxygen admixture is found to strongly influence the breakdown process and plasma conditions of a VDBD and a SDBD. [ABSTRACT FROM AUTHOR]