Photochemistry of Imidazole-2-carbaldehyde in Droplets as a Potential Source of H2O2 and Its Oxidation of SO2.

Hydrogen peroxide (H2O2) plays a crucial role as an oxidizing agent within the tropospheric environment, making a substantial contribution to sulfate formation in hydrated aerosols and cloud and fog droplets. Field observations show that high levels of H2O2 are often observed in heavy haze events and polluted air. However, the source of H2O2 remains unclear. Here, using the droplets formed in situ by the deliquescence of hygroscopic compounds under a high relative humidity (RH), the formation of H2O2 by the photochemistry of imidazole-2-carbaldehyde (2-IC) under ultraviolet irradiation was explored. The results indicate that 2-IC produces IM-C•-OH and IM-C•═O radicals via H transfer itself to its excited triplet state and generates H2O2 and organic peroxides in the presence of O2, which has an evident oxidizing effect on SO2, suggesting the potential involvement of this pathway in the formation of atmospheric sulfate. H2O2 formation is limited in acidic droplets or droplets containing ammonium ions, and no H2O2 is detected in droplets containing nitrate, whereas droplets containing citric acid have an obvious promotion effect on H2O2 formation. These findings provide valuable insights into the behaviors of atmospheric photosensitizers, the source of H2O2, and the formation of sulfate in atmospheric droplets.

Direct aqueous photochemistry of methylglyoxal and its effect on sulfate formation.

In recent years, among many oxidation pathways studied for atmospheric sulfate formation, the aqueous phase oxidation pathways of H2O2 and organic hydroperoxides (ROOHs) have attracted great scientific attention. Higher concentrations of H2O2 and ubiquitous ROOHs have been observed in atmospheric aqueous phase environments (cloud water, fog droplets, etc.). However, there are still some gaps in the study of their aqueous phase generation and their influences on sulfate formation. In this study, the aqueous phase photochemical reaction of methylglyoxal, a ubiquitous organic substance in the atmospheric aqueous phase, was studied under UV irradiation, and the generation of H2O2 and ROOHs in this system was investigated. It is found for the first time that the aqueous phase photolysis of methylglyoxal not only produces H2O2 but also produces ROOHs, and UV light and O2 are necessary for the formation of H2O2 and ROOHs. Based on the experimental results, the possible mechanism of aqueous phase photochemistry of methylglyoxal and the generation of H2O2 and ROOHs were proposed. The effect of aqueous phase photolysis of methylglyoxal on sulfate formation under different conditions was also investigated. The results show that the aqueous phase photolysis of methylglyoxal significantly promoted SO2 oxidation and sulfate formation, in which SO2 oxidation was realized by the generated H2O2, ROOHs and •OH radicals, and the importance of the formed ROOHs cannot be ignored. These results fill some gaps in the field of aqueous phase H2O2 and ROOHs production, and to a certain extent confirm the important roles of the aqueous phase photolysis of methylglyoxal and the formed H2O2 and ROOHs in the production of sulfate. The study reveals the new sources of H2O2 and ROOHs, and provides a new insight into the heterogeneous aqueous phase oxidation pathways and mechanisms of SO2 in cloud and fog droplets and haze particles.

Combined effects of high relative humidity and ultraviolet irradiation: Enhancing the production of gaseous NO2 from the photolysis of NH4NO3.

Free radicals and nitrogen-containing species produced by nitrate photolysis can affect various atmospheric chemical processes, and thereby the photochemical behavior of atmospheric nitrate aerosols has been attracting much attention. However, the photolysis mechanism of NH4NO3 and its products under different atmospheric conditions remain unclear. In this study, the effects of relative humidity (RH), pH, NH3, ultraviolet (UV) light intensity and halogen ions (Cl-, Br- and I-) on the photolysis of particulate NH4NO3 have been investigated through a flow tube reactor. The results show that RH can significantly enhance the production of gaseous NO2 from the photolysis of NH4NO3 when RH is higher than its deliquescence RH, but almost no NO2 is generated under dry conditions. Under high RH and UV light, the main product of NH4NO3 photolysis is NO2, rather than NO and HONO, and another main species HNO3 which mainly comes from the hydrolysis of product NO2 in the gas path was detected. Almost no NO2 and HNO3 are produced under high RH without UV light or low RH with UV light, showing the combined effect of high RH and UV irradiation on the photolysis of NH4NO3. In addition, under high RH, the lower the pH and the stronger the light intensity, the higher the NO2 production. Furthermore, surprising yields of NO and HONO are detected in the presence of halogen ions, especially in the presence of I-, indicating the important role of halogen ion in the nitrate photolysis. These results provide new insights into the photolysis of atmospheric nitrate aerosols, and may contribute to elucidating the formation and migration of atmospheric nitrate aerosols and the potential mechanisms of the occurrence and evolution of atmospheric pollution and ozone pollution.

Aqueous phase oxidation of bisulfite influenced by nitrate and its photolysis.

Nitrate aerosol is ubiquitous in the atmosphere. Nitrate in the particulate and aqueous phase can affect various atmospheric chemical processes through its hygroscopicity and photolysis. The impacts of nitrate photolysis on the heterogeneous oxidation of SO2 have been attracting attention. However, the influence of nitrate on heterogeneous aqueous phase formation of atmospheric sulfate aerosol is still not very clear. In this study, the effects of nitrate on aqueous phase oxidation of bisulfite under different conditions were investigated. Results show that nitrate photolysis can promote the oxidation of bisulfite to sulfate, especially in the presence of O2. It is found that pH plays a significant role in the reaction, and ammonium sulfate has significant impacts on the enhancement of aqueous phase sulfate production through regulating the pH of solution. An apparent synergism is found among halogen chemistry, nitrate and its photochemistry and S (IV) aqueous oxidation, especially the oxidation of halide ions by nitrate and its photolysis and by the intermediate products produced by the free radical chain oxidation of S (IV) in acidic solution, leading to the coupling of the redox cycle of halogen with the oxidation of bisulfite, which promotes the continuous aqueous oxidation of bisulfite and the formation of sulfate. In addition, the role of nitrate itself in the aqueous phase oxidation of bisulfite is revealed. These results provide a new insight into the heterogeneous aqueous phase oxidation pathways and mechanisms of SO2 in cloud and fog droplets and haze particles.