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Aiming at enhanced particulate matter (PM) removal of electrostatic precipitators (ESPs) in coal-fired power plants, a pulse energization power supply that generates high-voltage pulses superimposed on a high-voltage dc was designed. The integrated theories of corona discharge, particle charging, and removal were presented, and the pulse energization strategy was studied through fractional particle removal simulation. The conclusion of simulation stated that pulse energization could significantly improve particle charge with a maximum enhancement at a particle diameter of $20~\mu \text{m}$ , while the fractional particle removal efficiency shows a different distribution that removal of particles less than $2.5~\mu \text{m}$ had the most significant enhancement. Based on the design and simulations, a full-scale comparative operation study testified the potential of dc + pulse energization to enhance particle removal with a limited power consumption increase. Pulse energization was applied to different industrial ESPs with various design and operation parameters and shown multicondition adaptability in PM removal enhancement, with the emission reduction ranging from 45.48% to 58.00% and outlet concentration from 8.60 to 47.48 mg/Nm3, proving it a convenient and economical method in the performance boost of industrial ESPs. [ABSTRACT FROM AUTHOR]

OH radicals play an important role in pollutant removal in nonthermal plasmas. It is crucial to clarify the behavior of OH radicals in this process. A time-resolved 2-D OH radial distribution was investigated in a pulsed corona discharge by planar laser-induced fluorescence at atmospheric pressure and room temperature. The OH evolutions under different gas components were studied, and the evolution process was simulated. The OH decay processes were found to be divided into two periods: a fast decay period and a slow decay period. The O, N, and \HO2 are dominant radicals for OH generation and decay. The OH radicals are mainly generated near a nozzle electrode. The concentration variations of \O2, NO, and \H2\O in the background gas led to different OH density evolutions. The OH distribution zones were different as gas components varied. The maximum area of OH radical distribution after discharge decreased by 20\% as \O2 increased from 5\% to 8 \%, and it decreased by 69 \% as NO (150 ppm) was added into the background gas. [ABSTRACT FROM PUBLISHER]

This paper investigated the enhancement of plasma on dimethyl sulfide (DMS) removal over commercial V-W/Ti catalysts. The effects of catalyst composition, discharge power, and gas temperature on DMS removal in the plasma-based system were analyzed. The results showed that the V0.9–W/Ti catalyst exhibited the best performance toward DMS removal due to its highest reducibility among the employed samples. The introduction of plasma exhibited a synergistic effect on catalysts and significantly enhanced the removal of DMS over the studied temperature range, especially in high discharge power cases. The activation energy Ea of DMS removal in the presence of plasma was dramatically reduced to less than 10% of the catalysis only case, indicating different DMS removal pathways in plasma-activated catalysis system. The reaction mechanisms of DMS were also discussed based on the reaction products. [ABSTRACT FROM PUBLISHER]