Adsorbed nitrate is ubiquitous in the atmosphere, and it can undergo photolysis to produce oxidizing active radicals. Nitrate photolysis may be coupled with the oxidation conversions of atmospheric gaseous pollutants. However, the processes involved remain poorly understood. In this study, the impact of adsorbed nitrate on the heterogeneous oxidation of SO on α-FeO was investigated in the absence and presence of simulated solar irradiation by using in situ Diffuse Reflectance Infrared Fourier Transform Spectroscopy (DRIFTS). The results indicate that for α-FeO particles with no adsorbed nitrate, the formation of adsorbed sulfate on humid particles is stronger than that on dry particles. Meanwhile, light can also promote the heterogeneous conversion of SO and the formation of sulfate on dry particles because α-FeO is a typical photocatalyst. However, the heterogeneous conversion of SO on humid α-FeO particles is somewhat suppressed under light, suggesting the occurrence of photoinduced reductive dissolution. For the heterogeneous conversion of SO on α-FeO particles with adsorbed nitrate, the formation of sulfate on humid particles is still higher than that on dry particles. For the dry α-FeO particles with adsorbed nitrate, light promotes the formation of adsorbed sulfate. For the humid α-FeO particles with adsorbed nitrate, the heterogeneous conversion of SO under light is stronger than that under no light, indicating that the photolysis of adsorbed nitrate is coupled with the oxidation of SO and the formation of sulfate. The consumption of adsorbed nitrate and the formation of adsorbed NO are observed during the introduction of SO. A possible mechanism for the impact of adsorbed nitrate on the heterogeneous conversion of SO on α-FeO particles is proposed, and atmospheric implications based on these results are discussed.
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http://dx.doi.org/10.1016/j.scitotenv.2018.08.295 | DOI Listing |
Environ Res
January 2025
State Key Laboratory of Marine Pollution and Department of Chemistry, City University of Hong Kong, Tat Chee Avenue, Hong Kong, Kowloon, 999077, China; School of Energy and Environment, City University of Hong Kong, Tat Chee Avenue, Hong Kong, Kowloon, 999077, China.
Bisphenol A (BPA) is a commonly used endocrine-disrupting chemical found in high levels in wastewater worldwide. Aerobic denitrification is a promising alternative to conventional nitrogen removal processes. However, the effects of BPA on this novel nitrogen removal process have rarely been reported.
View Article and Find Full Text PDFEnviron Res
December 2024
Integrated Science and Technology Research Center, Faculty of Technology and Environment, Prince of Songkla University, Phuket Campus, Kathu, Phuket, 83120, Thailand. Electronic address:
Nitrate is a crucial nutrient in the natural nitrogen cycle. However, human activities have elevated nitrate levels in aquatic ecosystems beyond natural thresholds, posing risks to human health and the environment. In this work, ZnCl-doped mesoporous silica nanoparticles (ZnCl@MSN) were synthesized using a one-pot preparation method, leading to a streamlined process with reduced time and energy consumption.
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January 2025
Institute of Chemistry, Federal University of Mato Grosso do Sul, Avenida Senador Filinto Muller 1555, Campo Grande, Mato Grosso do Sul 79074-460, Brazil.
There has been huge interest among chemical scientists in the electrochemical reduction of nitrate (NO) to ammonia (NH) due to the useful application of NH in nitrogen fertilizers and fuel. To conduct such a complex reduction reaction, which involves eight electrons and eight protons, one needs to develop high-performance (and stable) electrocatalysts that favor the formation of reaction intermediates that are selective toward ammonia production. In the present study, we developed and applied CoO/graphene nanoribbon (GNR) electrocatalysts with excellent properties for the effective reduction of NO to NH, where NH yield rate of 42.
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China Auto Information Technology Co., Ltd, Tianjin 300300, People's Republic of China.
ACS Earth Space Chem
December 2024
University of Iowa, Iowa City, Iowa state 52242, United States.
Environmental films form when airborne particles and molecular species adsorb on solid surfaces. Recent studies have characterized these films but overlook how collection methods and host-surface character (orientation, chemical functionality, or height) change the deposition process. In this work, environmental films are collected at a rural location on gold and silicon surfaces (water contact angles of ca.
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