ABSTRACT
In recent years, there has been a growing concern about air pollution and its impact on the air quality and human health, especially for fine particulate matter (PM2.5) and its associated secondary aerosols in urban areas. This study conducted a year-long field campaign to collect PM2.5 samples day and night in an urban area of central Taiwan. Higher PM2.5 mass concentrations were observed in winter (27.7 ± 9.7 µg/m3), followed by autumn (22.5 ± 8.3 µg/m3), spring (19.2 ± 6.4 µg/m3), and summer (11.0 ± 3.1 µg/m3). The dominant formation mechanism of secondary inorganic aerosols was heterogeneous reactions of NO3- at night and homogeneous reactions of SO42- during the day. Additionally, significant correlations were observed between aerosol liquid water content (ALWC) and NO3- during nighttime, indicating the importance of aqueous-phase NO3- formation. The role of aerosol acidity was explored and a unique alkaline condition was found in spring and summer, which showed lower PM2.5 concentrations than the neutralized condition. Under the neutralized condition, higher PM2.5 concentrations were commonly found when combining the ammonium-rich regime with molar ratios of [NO3-]/[SO42-] exceeding 1.6, suggesting the importance of reducing both NH3 and NOx. Furthermore, the results showed that reducing NH3 should be prioritized under high temperature conditions, while reducing NOx became important under low temperature conditions. Clustering of backward trajectories showed that long-range transport could enhance the formation of secondary aerosols, but local emissions emerged as the main factor driving high PM2.5 concentrations. This study provides insights for policymakers to improve air quality, suggesting that different mitigation strategies should be formulated based on meteorological variables and that using clean energy for vehicles and electricity generation is important to alleviate air pollution.
ABSTRACT
This study aimed to explore the oxidation and transformation of the cephalosporins cefotaxime (CTX), cephalexin (CFX), cephradine (CFD), cephapirin (CFP) and cefazolin (CFZ) by δ-MnO2. The results showed that the MnO2 oxidation rate was promoted by environmental factors such as higher MnO2 loading, lower initial cephalosporin concentration and lower solution pH. The inhibitory effect occurred in the presence of dissolved organic matter and dissolved cations (inhibitory capacity: Mn2+ > Ca2+ > Mg2+ > Fe3+). Total organic carbon analysis indicated that the transformation byproducts of the cephalosporins are less reactive and persistent under MnO2 oxidation. Twelve transformation byproducts (9 CFP byproducts and 3 CTX byproducts) were identified, and two oxidative transformation pathways were proposed: one occurred in the cephem for CFP, and the other occurred at the substituent at the amine position for CTX. The effect of solar light on the oxidation of the five cephalosporin antibiotics by δ-MnO2 was also investigated, and the results indicated that the initial dissolution rate of δ-MnO2 under sunlight was approximately eight times faster than that in the dark in the presence of CFP.
