Pollution characteristic and variation trend of atmospheric carbonyls were investigated in November during the 2014 Beijing APEC. Formaldehyde, acetaldehyde and acetone were the dominant carbonyls, accounting for 82.66% of total carbonyls, and especially, formaldehyde accounted for 40.12% of total carbonyls. Atmospheric concentrations of total carbonyls decreased by around 64.10% after the clean air policy was carried out during the Beijing APEC, and the variation trend of carbonyls showed a similar pattern to those of other pollutants like PM₂.₅ during the APEC. Strong correlations (R² of 0.67-0.98) were observed among formaldehyde, acetaldehyde, acetone and total carbonyls during and after the APEC, indicating that they had similar sources; however, poor correlations (R² of -0.11-0.42 and 0.16-0.94, respectively) were observed before the APEC, implying different emission sources for ambient carbonyls. The calculated ratios of C1/C2, C2/C3 and OC/EC indicated that both vehicles and coal emissions were responsible for atmospheric carbonyls before the APEC, and emissions from coal burning were the major contributor to atmospheric carbonyls during and after the APEC, especially after the APEC.
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Chemosphere
December 2024
Universidade Federal do Rio de Janeiro, Instituto de Química, Rio de Janeiro, RJ, 21941-909, Brazil. Electronic address:
Peri-urban conserved natural or semi-natural areas provide several ecosystem services and assist in reducing air pollution in cities. The aim of this study is to assess the contribution to the improvement of air quality of a small area (<1 km) adjacent to a city in the Metropolitan Region of Rio de Janeiro (Brazil), which is seriously affected by vehicular and industrial emissions of pollutants. Hydrocarbon (HC) and carbonyl compounds (CC) levels were determined, by employing TO-15 and TO-11A US EPA Methods, respectively, in both the urban and green areas.
View Article and Find Full Text PDFJ Am Chem Soc
December 2024
School of Chemistry, University of New South Wales, Kensington, NSW 2052, Australia.
Hydrofluoroolefins (HFOs) and hydrochlorofluoroolefins (HCFOs) are the leading synthetic replacements for compounds successively banned by the Montreal Protocol and amendments. HFOs and HCFOs readily decompose in the atmosphere to form fluorinated carbonyls, including CFCHO in yields of up to 100%, which are then photolyzed. A long-standing issue, critical for the transition to safe industrial gases, is whether atmospheric decomposition of CFCHO yields any quantity of CHF (HFC-23), which is one of the most environmentally hazardous greenhouse gases.
View Article and Find Full Text PDFDalton Trans
December 2024
Institut für Anorganische und Analytische Chemie und Freiburger Materialforschungszentrum (FMF), Albert-Ludwigs-Universität Freiburg, Albertstr. 21, 79104 Freiburg, Germany.
The reaction of Ag with Ru(CO) in a CO atmosphere under concommittant irradiation with UV-light yields a salt of the metal-only Lewis-pair [Ag{Ru(CO)}]. Switching the silver cation for a more process-selective deelectronator yields a salt of the homoleptic transition metal carbonyl cation [Ru(CO)], which fills the gap between the known cations [Ru(CO)] and [Ru(CO)]. The amount of π-backdonation in this series was studied by a combination of vibrational spectroscopy and computed relaxed force constants.
View Article and Find Full Text PDFPhys Chem Chem Phys
December 2024
Department of Chemistry, University of Helsinki, FI-00014 Helsinki, Finland.
Quantum chemical calculations were employed to construct Jablonski diagrams for a series of phenolic carbonyls, including vanillin, iso-vanillin, 4-hydroxybenzaldehyde, syringaldehyde, and coniferyl aldehyde. These molecules can enter the Earth's atmosphere from forest fire emissions and participate in photochemical reactions within the atmospheric condensed phase, including cloud and fog droplets and aqueous aerosol particles. This photochemistry alters the composition of light-absorbing organic content, or brown carbon, in droplets and particles through the formation and destruction of key chromophores.
View Article and Find Full Text PDFSmall
December 2024
Key Laboratory of Organic Optoelectronics and Molecular Engineering of Ministry of Education, Department of Chemistry, Laboratory of Flexible Electronics Technology, Tsinghua University, Beijing, 100084, P. R. China.
Lead halide perovskites hold immense promise for optoelectronic applications but still suffer from instability caused by defects. The defects are mainly generated from the film fabrication processes and halide ion migration during long-term storage. Here, a synergistic doping strategy is proposed to enhance the stability of perovskites.
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