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1.
J Environ Sci (China) ; 66: 188-198, 2018 Apr.
Artículo en Inglés | MEDLINE | ID: mdl-29628086

RESUMEN

PM2.5 samples were collected in Zhengzhou during 3years of observation, and chemical characteristics and source contribution were analyzed. Approximately 96% of the daily PM2.5 concentrations and annual average values exceeded the Chinese National Ambient Air Quality Daily and Annual Standards, indicating serious PM2.5 pollution. The average concentration of water-soluble inorganic ions was 2.4 times higher in heavily polluted days (daily PM2.5 concentrations>250µg/m3 and visibility <3km) than that in other days, with sulfate, nitrate, and ammonium as major ions. According to the ratio of NO3-/SO42-, stationary sources are still the dominant source of PM2.5 and vehicle emission could not be ignored. The ratio of secondary organic carbon to organic carbon indicated that photochemical reactivity in heavily polluted days was more intense than in other days. Crustal elements were the most abundant elements, accounting for more than 60% of 23 elements. Chemical Mass Balance results indicated that the contributions of major sources (i.e., nitrate, sulfate, biomass, carbon and refractory material, coal combustion, soil dust, vehicle, and industry) of PM2.5 were 13%, 16%, 12%, 2%, 14%, 8%, 7%, and 8% in heavily polluted days and 20%, 18%, 9%, 2%, 27%, 14%, 15%, and 9% in other days, respectively. Extensive combustion activities were the main sources of polycyclic aromatic hydrocarbons during the episode (Jan 1-9, 2015) and the total benzo[a]pyrene equivalency concentrations in heavily polluted days present significant health threat. Because of the effect of regional transport, the pollution level of PM2.5 in the study area was aggravated.


Asunto(s)
Contaminantes Atmosféricos/análisis , Monitoreo del Ambiente , Material Particulado/análisis , Contaminación del Aire/estadística & datos numéricos , China , Hidrocarburos Policíclicos Aromáticos/análisis , Estaciones del Año , Emisiones de Vehículos/análisis
2.
Sci Total Environ ; 946: 174391, 2024 Oct 10.
Artículo en Inglés | MEDLINE | ID: mdl-38955272

RESUMEN

Atmospheric hydrogen peroxide (H2O2), as an important oxidant, plays a key role in atmospheric chemistry. To reveal its characteristics in polluted areas, comprehensive observations were conducted in Zhengzhou, China from February 22 to March 4, 2019, including heavy pollution days (HP) and light pollution days (LP). High NO concentrations (18 ± 26 ppbv) were recorded in HP, preventing the recombination reaction of two HO2• radicals. Surprisingly, higher concentrations of H2O2 were observed in HP (1.5 ± 0.6 ppbv) than those in LP (1.2 ± 0.6 ppbv). In addition to low wind speed and relative humidity, the elevated H2O2 in HP could be mainly attributed to intensified particle-phase photoreactions and biomass burning. In terms of sulfate formation, transition-metal ions (TMI)-catalyzed oxidation emerged as the predominant oxidant pathway in both HP and LP. Note that the average H2O2 oxidation rate increased from 3.6 × 10-2 in LP to 1.1 × 10-1 µg m-3 h-1 in HP. Moreover, the oxidation by H2O2 might exceed that of TMI catalysis under specific conditions, emerging as the primary driver of sulfate formation.

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