Abstract

The fixation of atmospheric nitrogen into valuable compounds through reactive plasma processes has attracted intense interests due to its easy operation and compatibility with distributed renewable energy sources. However, practical implementation of plasma-assisted nitrogen fixation is hampered because of its relatively low throughput, which is dominantly limited by the unclear underlying mechanisms. In this study, effort was focused on the in situ production of key species in a DC-driven warm air glow discharge at atmospheric pressure with the help of advanced laser spectroscopic diagnostics. Laser Rayleigh scattering was applied to determine the gas temperature distribution in the discharge column. And mid-infrared quantum cascade laser absorption spectroscopy and one/two-photon absorption laser-induced fluorescence were performed on molecular nitric oxide (NO), atomic oxygen and nitrogen (O, N) for their absolute densities in the discharge. It is found that the spatial distributions of gas temperature, O and N atoms show peaks in the hot discharge center. In contrast, a hollow ‘doughnut’ shape characterized by the NO molecule was observed, particularly under conditions of high discharge current but low airflow rate. The steady-state simulation shows that the hollow pattern of NO is dominantly induced by the radial diffusion of species due to the steep spatial gradient of gas temperature in the discharge cross-section. Moreover, the reverse conversion by atomic N leads to a negative effect on the NO synthesis, especially at the discharge center where the N density and gas temperature are high. From the steady-state modeling, a similar hollow distribution of NO2 was depicted in the air glow discharge. These results demonstrate the strong dependence on atomic O for the major formation process of NO, and the importance of suppressing the reverse paths dominated by atomic N for higher NO production in the studied warm air plasma.

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