Variations of Particle Size Distribution, Black Carbon, and Brown Carbon during a Severe Winter Pollution Event over Xi'an, China

Real-time particulate matter (PM) size distributions, 4-hour time resolution, PM2.5, carbonaceous materials, and their optical properties were measured during a severe pollution event in Xi'an, China High PM2.5 /PM10 ratios were observed on both pollution (0.83) and non-pollution (0.73) days, emphasizing the abundance of fine particles during sampling days. The particle number (PN) first peaked with a wide size range (30-100 nm) before morning rush hours (approximately 01:00-05:00) on pollution and non-pollution days, demonstrating that PN was governed by the accumulation of freshly emitted diesel particles and characterized by distinct aerosol condensation growth. By contrast, the second peak time and size range differed between pollution and non-pollution days because of different formation mechanisms The light-absorbing coefficients of both black carbon (BC, b(abs-880nm,BC)) and brown carbon (BrC, b(abs-370nm, BrC)) were high on pollution days and decreased to approximately half of those values on non-pollution days, indicating that the degree of light absorption is reduced by rain. The diurnal variation in b(abs-880nm, BC) pollution peaked with traffic on January 1 and 2. By contrast, it remained in relatively stable and high ranges (120-160 Mm(-1)) in the second period (January 3-5) without traffic peaks, illustrating that the dominant sources changed even during the same pollution period. High values of both b(abs-370nm, BrC) and b(abs-880nm,) (BC )coincided in the afternoon and evening due to emissions from primary sources, and abundant aqueous secondary organic carbon, respectively. A highly variable mass absorption coefficient of BrC also indicated the variety of fuel combustion sources of primary BrC in Xi'an

Day-Night Differences, Seasonal Variations andSource Apportionment of PM10-Bound PAHs overXi’an, Northwest China

Day-night PM10-bound PAHs were studied at an urban site of Xi’an from 20 December 2006 to 28 October 2007. The annual mean concentration of nighttime PAHs (285.0 ng m−3) was higher than that in daytime (239.4 ng m−3). A significant difference of PAH concentrations between daytime and nighttime was found in autumn with a coefficient of divergence (CD) of 0.23 (significant level 0.2). However, no distinct difference was observed in other seasons (with CD values < 0.2), although the difference of PAHs partition capacity in PM10 between daytime and nighttime was significant in the four seasons. Remarkable seasonal variations were observed in the total PAH levels, with a highest mean concentration of 344.6 ng m−3 in winter and a lowest mean concentration of 177 ng m−3 in summer. Positive matrix factorization results revealed that residential emission for heating is the major contributor of the elevated PAH levels in winter, accounting for 49% of the total PAH levels. The coal combustion including industrial and residential usage, contributed over 40% of the PAH emissions in PM10 of Xi’an during the one-year sampling period. These results can provide guidance for taking measures in reducing PAHs levels in the air

Saccharides in summer and winter PM2.5 over Xi'an, Northwestern China: Sources, and yearly variations of biomass burning contribution to PM2.5

Saccharides are important constituents in atmospheric aerosols but studies in northwestern China are still very limited. Here, we have measured anhydrosugars (levoglucosan, mannosan and galactosan), primary sugars (glucose, fructose, sucrose and trehalose), and sugar alcohols (arabitol, mannitol, sorbitol and inositol) in ambient PM2.5 samples during summer and winter in Xi&#39;an city, northwestern China. The abundance of total saccharides showed no clear seasonal variation, but apparent distinctions on the levels of the three categories and individual saccharide compounds were found. Primary sugars and particularly sucrose were dominant in summer. In contrast, levoglucosan was the predominant species in winter, contributing 60% of total saccharides. Source apportionment by positive matrix factorization revealed that airborne pollen was a major source of PM2.5 associated-saccharides in summer, accounting for 35% of total saccharides; while biomass burning activities contributed to 60% of the winter saccharides. Furthermore, an increasing trend of biomass/biofuel burning contribution to winter PM2.5 was observed in comparison with previous studies in Xi&#39;an, suggesting a change in emission sources may be underway in northwestern China.</p

Optical property variations from a precursor (isoprene) to its atmospheric oxidation products

Isoprene is a crucial precursor of secondary organic aerosols (SOAs) that reacts with radicals or oxidants such as OH, O3, and NO3. The reaction mechanisms under various conditions have been elucidated through years of research. In this study, the UV&ndash;vis light absorptive ability of oxydates for isoprene was calculated at the PBE1PBE/6-311g (d) level using Gaussian 09. The results indicated that reactions of isoprene with OH and O3 would produce less absorptive organics; the intensity of the absorption peaks and the maximum absorption wavelength decreased relative to those of the precursor. The oxydates formed from isoprene through an NO3-initiated reaction had different light absorption properties. The optical properties of the oxydates exhibited a bathochromic shift and hyperchromic effect relative to those of the precursor. NO3 mainly originated from vehicular traffic, indicating that anthropogenic activity heavily affected the formation of oxydates and light absorption. The light absorption properties and irradiation effect of SOAs caused by isoprene heavily depended on the reaction route. Transformation of functional groups was the dominated factor in photobleaching and photoenhancement of oxidative products. This study provides a detailed mechanism that explains the changes in optical absorption properties during isoprene oxidation.</p