The interplay between sulfur and iron holds significant importance in their atmospheric cycle, yet a complete understanding of their coupling mechanism remains elusive. This investigation delves comprehensively into the evolution of reactive oxygen species (ROS) during the interfacial reactions involving sulfur dioxide (SO) and iron oxides under varying relative humidity conditions. Notably, the direct activation of water by iron oxide was observed to generate a surface hydroxyl radical (•OH).
View Article and Find Full Text PDFIn this work, we developed an alternative calibration method for measuring NO with an iodide adduct mass spectrometer (I-CIMS). In this calibration method, NO is heated and then quantified based on the decrease in the amount of NO due to its reaction with the pyrolysis product (NO). This alternative calibration method was compared with the commonly used method utilizing NO analyzers equipped with a photolytic converter, which gauge NO reduction as a result of its reaction with O to quantify NO.
View Article and Find Full Text PDFDuring the COVID-19 lockdown in the Beijing-Tianjin-Hebei (BTH) region in China, large decrease in nitrogen oxides (NO) emissions, especially in the transportation sector, could not avoid the occurrence of heavy PM pollution where nitrate dominated the PM mass increase. To experimentally reveal the effect of NO control on the formation of PM secondary components (nitrate in particular), photochemical simulation experiments of mixed volatile organic compounds (VOCs) under various NO concentrations with smog chamber were performed. The proportions of gaseous precursors in the control experiment were comparable to ambient conditions typically observed in the BTH region.
View Article and Find Full Text PDFAngew Chem Int Ed Engl
June 2023
N O is an important intermediate in the atmospheric nitrogen cycle. Using a flow tube reactor, N O was found to be released from the TiO surface during the photocatalytic oxidation of NO , revealing a previously unreported source of N O . The rate of N O release from TiO was dependent on the initial NO concentration, relative humidity, O /N ratio, and irradiation intensity.
View Article and Find Full Text PDFSecondary organic aerosol (SOA) formation originating from the emission of anthropogenic volatile organic compounds (VOCs) makes a significant contribution to fine particulate matter (PM) pollution in urban areas. Investigation on the SOA formation potential (SOAFP) can help us understand the contribution of different sources to SOA formation. To characterize the SOAFP of ambient air from anthropogenic VOCs in the urban area of Beijing, field observation was implemented using a twin oxidation flow reactor (Twin-OFRs) system in the winters of 2016 and 2017.
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