[Regional PM pollution in Beijing and surrounding area during summertime].

The air quality in Beijing and surrounding area is influenced by local emission and regional transport. To study the characteristics of regional pollution, PM (particulate matter) samples were collected simultaneously at 4 sites including Tsinghua University (TH) and Miyun reservoir (MY) in Beijing, Renqiu (RQ, Hebei Province), and Shangdu (SD, Inner Mongolia) during August, 2007, and temporal/spatial distributions of PM2.5 mass concentrations along with 22 elements in TSP were characterized. PM2.5 mass concentrations were quite different at 4 sites, following the sequence as RQ > TH > MY > SD. The highest concentrations of pollution-derived elements S, Zn, Pb, Cu, As, Sb, Ni, Cd, In, Se were found in RQ, showing the most intensive anthropogenic influence around this region, and their lowest variation indicated that the pollution mostly came from local sources. Controlled by the meteorological factors, highest daily variations of these elements were found at SD with relative lower concentrations. The correlation coefficients of S, Pb, Cd, In, As, Zn concentrations between TH and MY were all higher than 0.70, which implies similar sources for these elements at the 2 sites in Beijing. At the beginning and the end of the Sawtooth pollution episode in Beijing, concentrations of most elements in Miyun were comparable with the lowest concentrations at Shangdu observed during the sampling period, which means Miyun could well represent the regional characteristics of clean air mass from the northwest. Uniform spatial distribution of high sulfate was found (about 10 microg/m3) at the peaks of Sawtooth episode, which implies the important contribution from secondary aerosol during the regional pollution. Variable sources of PM at each site and their regional influence were discussed based on the different characteristics of elemental enrichment factors.

Trends in hazardous trace metal concentrations in aerosols collected in Beijing, China from 2001 to 2006.

Daily observations of hazardous trace metal concentrations in aerosols in Beijing, China were made in the period from 2001 to 2006. We considered coal combustion as a major source of some anthropogenic metals by achieving a correlation analysis and by investigating enrichment factors and relative composition of metals. A possible extra source of some specific metals, such as Cu and Sb, was brake abrasion particles, however, we did not think the transport-related particle was a major source for the hazardous anthropogenic metals even though they could originate from vehicle exhaust and brake/tire abrasion particles. A time-trend model was used to describe temporal variations of chemical constituent concentrations during the five-year period. Several crustal elements, such as Al, Ti, V, Cr, Mn, Fe, and Co, did not show clear increases, with annual rates of change of -15.2% to 3.6%. On the other hand, serious increasing trends were noted from several hazardous trace metals. Cu, Zn, As, Cd, and Pb, which are derived mainly from anthropogenic sources, such as coal combustion, showed higher annual rate of change (4.9-19.8%, p<0.001) according to the regression model. In particular, the Cd and Pb concentrations increased remarkably. We hypothesize that the trend towards increasing concentrations of metals in the air reflects a change that has occurred in the process of burning coal, whereby the use of higher temperatures for coal combustion has resulted in increased emissions of these metals. The increasing use of low-rank coal may also explain the observed trends. In addition, nonferrous metal smelters are considered as a potential, albeit minor, reason for the increasing atmospheric concentrations of anthropogenic hazardous metals in Beijing city.

Diurnal variation of number concentration and size distribution of ultrafine particles in the urban atmosphere of Beijing in winter.

Number concentration and distribution of airborne particles in the size range 5.6 to 560 nm diameter were measured in Beijing for a 15-d period in winter 2005. Daily average number concentrations of nucleation mode (5.6-20 nm), Aitken mode (20-100 nm), and accumulation mode (100-560 nm) particles, and total particles were 17500, 32000, 4000, and 53500 cm(-3), respectively. Average particle size distribution was monomodal with a mode diameter of about 40 nm at night and bimodal with mode diameters of about 10 and about 40 nm during the daytime. New particle formation events, which were connected to diurnal variation of nucleation mode particles, were observed in more than half of the observation days. The events often started around 10:00-11:00 Chinese Standard Time (CST) and ended up after 3-4 h. Concentrations of Aitken and accumulation mode particles increased from midnight and reached their maxima at about 10:00 CST, and then decreased and became the lowest in the afternoon. Analysis of diurnal cycles in traffic volume and meteorological parameters revealed that the accumulation of the particles in Aitken and accumulation modes in the morning was influenced by formation of an inversion and increase in vehicle emission, and dispersion of such particles in the afternoon was associated with more effective vertical mixing and higher wind speed.

[Characteristics of polycyclic aromatic hydrocarbons (PAHS) on airborne particulates in Beijing].

Total suspended particulates (TSP) samples were collected from Sep., 2003 to Jul., 2004 in Beijing, and 15 kinds of PAHs, ranging from 3 to 7 rings were analyzed. The maximum concentrations sigma PAHs and BaP were 705 ng/m3 and 52 ng/m3 respectively. Average sigma PAHs concentrations in four seasons were 46 ng/m3, 16 ng/m3, 52 ng/m3 and 268 ng/m3 respectively; and the average BaP concentrations in four seasons were 2.8 ng/m3, 0.23 ng/m3, 3.3 ng/m3, 16 ng/m3 respectively. Regarding to the meteorological parameters, precipitation distinctly lowered the concentration; in heating period, PAHs concentrations fall with the temperature goes up, but there is no obvious relation between concentration and temperature in non-heating period; the increase of wind speed level causes the decrease of PAH concentrations in the heating period, but relation between PAH concentrations and wind speed varied with aromatic rings of PAHs and levels of wind speed in the non-heating period.

Polycyclic aromatic hydrocarbons (PAHs) in the aerosol in Beijing, China, measured by aminopropylsilane chemically-bonded stationary-phase column chromatography and HPLC/fluorescence detection.

We developed a useful analytical method for the determination of polycyclic aromatic hydrocarbons (PAH) concentrations in the aerosol of China. We used an accelerated solvent extraction (ASE) method for the extraction of PAHs from the aerosol samples, in order to reduce the extraction time and the solvent volume used. The optimum purification method was developed, with aminopropylsilane chemically-bonded stationary-phase column chromatography, in order to remove many co-extractives which cannot be removed by conventional purification methods using silica-gel column chromatography. HPLC/fluorescence detection (FLD) was adopted as the analytical method, because it has very high sensitivity to PAH and it is easy to install, operate, and maintain as compared with GC/MS. With the analytical method developed in this study, the recovery and precision (RSD) for most of the PAHs ranged from 75% to 129% and from 2.8% to 22.7%, respectively. The concentrations of PAHs in the aerosol samples collected from October 2003 to April 2005 in Beijing, China were determined using the newly developed method. SigmaPAHs, which is the sum of the concentrations of all detected PAHs, was 177.8 +/- 239.9 ng m(-3) (n = 64). The SigmaPAHs concentration in the heating season (305.1 +/- 279.0 ng m(-3), n = 33) was 7.2 times higher than that in the non-heating season (42.3 +/- 32.0 ng m(-3), n = 31). These strong seasonal variations in atmospheric PAH concentration are possibly due to coal combustion for residential heating in winter.

Characteristics of carbonaceous aerosols in Beijing, China.

Carbonaceous aerosols and PM10 were monitored from September 8 to November 30, 2002, in a semi-urban site (Tsinghua University) in Beijing. Daily concentrations of OC and EC ranged from 7.1 to 65.9 microgCm(-3) and from 1.3 to 26.1 microgCm(-3), with the overall average concentrations of 21.2 microgCm(-3) and 7.3 microgCm(-3), respectively. The diurnal variation of carbonaceous concentrations on 2 h basis presented two-peak trend, which was attributed to the cooperative effect of local meteorological conditions and anthropogenic sources such as traffic exhaust and human outdoor activities. Daily average OC/EC ratio varied between 1.5 and 5.3 with an average of 3.0. Strong correlation between OC and EC (R2=0.8) indicated that their main sources were common. The frequency of OC/EC ratio presented Gaussian normal distribution trend in fall, of which the peak value appeared in the range of 2.8-5. In winter, it presented bi-peak mode, with the first peak near 1.4-1.6, and the second between 2.8 and 5. The high value (2.8-5) implied the SOC formation in both seasons, and the low one probably suggested the primary OC/EC ratio from coal burning in winter. Averagely, PM10 and carbonaceous species exhibited higher concentrations in Wednesday than in other weekdays, which could be ascribed to the low wind speed (1.6 ms(-1)) and high humidity (62.9%). OC was the abundant component accounting for 76% of TC. OC and EC contributed 15% and 5% to PM10, respectively. The estimation on a minimum OC/EC ratio (1.5) basis showed that SOC accounted more than 50% for the total organic carbon. Even in winter, the SOC contribution to OC was also significant, as high as 40%.