Search

To elucidate the characteristics of VOCs chemical components during heavy pollution episodes, hourly online VOCs data derived from 11 heavy pollution events in Tianjin from 2019 to 2020 were employed. The positive matrix factorization （PMF） and conditional bivariate probability function （CBPF） were employed to analyze the sources of VOCs during heavy pollution episodes. The results indicated that the average VOCs volume fraction during these episodes was recorded at 35.7×10 -9 . Furthermore, it was observed that during the winter emergency response period, there was a discernible increase in the volume fraction of VOCs when compared to that during the autumn season. Specifically, there was a notable upswing of 48% in the olefins category, whereas alkanes registered a 4% increase. Additionally, the VOCs component structure changed significantly during the heavy pollution episodes. During the orange warning period, the proportion of alkanes increased by 36%, and the proportion of acetylene decreased by 32%. During the yellow warning period, the proportion of alkanes increased by 14%, and the proportion of acetylene decreased by 5%. During the emergency response period, motor vehicle emission sources, natural gas evaporative sources, and solvent use sources were the main contributors of VOCs in environmental receptors, contributing 17.5%, 15.4%, and 15.2%, respectively. Compared with that during the period antecedent to the emergency response, the contribution of vehicle emission sources and diesel volatile sources to VOCs in environmental receptors decreased by 2.0% to 5.5% and 2.1% to 6.6%, respectively, and the contribution of solvent use sources decreased by 0.2% to 2.4% during the yellow warning period. During the orange warning period, the contribution of motor vehicle emission sources was reduced by 0.1% to 8.3%, and the contribution of solvent use sources was reduced by 0.5% to 6.2%.

Fugitive dust poses an important contribution to urban air particulate matter in China. To further improve the level of dust pollution prevention and control, the emission and contribution characteristics of urban fugitive dust were summarized; the main causes of dust pollution were analyzed; and the key links, key indicators, and main measures for prevention and control were clarified, so as to further improve the concept of "accurate dust control." Among all types of fugitive dust sources, road dust and construction dust were the main emission and contribution sources, among which road dust was more prominent. Production activities, vehicle disturbances, and wind erosion were the main dust-generating links of various dust sources. Silt loading was taken as the key control index for road dust prevention and control, whereas silt loading and bare soil (or material) areas were taken as the key control index for construction and other dust sources. Around the key indicators, three main ways to control the road dust and six main measures to control the construction and other dust sources were defined. In addition, some suggestions on the necessary supporting measures for dust control were put forward, so as to provide a comprehensive and beneficial reference for the practical application of dust control in Chinese cities.

Few efforts have been made to elucidate the influence of weather conditions on the fate of semivolatile organic compounds (SOCs). Here, daily fine particulate matter (PM 2.5 ) during clear, haze, and fog episodes collected in the winter in Beijing, China was analyzed for polycyclic aromatic hydrocarbons (PAHs), brominated flame retardants (BFRs), and organophosphate flame retardants (OPFRs). The total concentrations of PAHs, OPFRs, and BFRs had medians of 45.1 ng/m 3 and 1347 and 46.7 pg/m 3 , respectively. The temporal pattern for PAH concentrations was largely dependent on coal combustion for residential heating. OPFR compositions that change during colder period were related to enhanced indoor emissions due to heating. The mean concentrations of SOCs during haze and fog days were 2-10 times higher than those during clear days. We found that BFRs with lower octanol and air partition coefficients tended to increase during haze and fog episodes, be removed from PM 2.5 during clear episodes, or both. For PAHs and OPFRs, pollutants that are more recalcitrant to degradation were prone to accumulate during haze and fog days. The potential source contribution function (PSCF) model indicated that southern and eastern cities were major source regions of SOCs at this site.

Light absorption properties of water-soluble organic carbon (WSOC) were investigated in the urban area of Guangzhou. The fine particulate matter (PM₂.₅) and size-segregated samples were collected in September and December of 2014 and January of 2015. The variation of absorption with wavelength of WSOC was characterized by the absorption Angström exponent (AAEabs). The AAE values of WSOC in PM₂.₅ were 3.72 ± 0.41 in autumn and 3.91 ± 0.70 in winter, which were lower than those in Beijing and north America. The mass absorption efficiency (MAE) of WSOC at 365 nm wavelength was 0.52 m² · g⁻¹ in autumn and 0.92 m² · g⁻¹ in winter, exhibiting distinct variations between autumn and winter. In winter, the MAEwsoc values exhibited a decreasing trend with increasing particle size, and all size-segregated MAE(WSOC) values in autumn were lower than those in winter, particularly for the particles < 0.95 µm, suggesting more contribution of the secondary formation to WSOC. Comparing the MAE values of elemental carbon (EC) and WSOC, it could be found that the contribution of WSOC to the light extinction of particles couldn't be ignored when the particles were mainly emitted from primary sources.

In this study, PM2.5 samples were collected at four heights (10m, 40m, 120m and 220m) at a meteorological tower in the daytime and nighttime during the heating season in Tianjin, China. The vertical variation and diurnal variability of the concentrations of PM2.5 and main chemical compositions were analyzed in clear days and heavy pollution days. Generally, mass concentrations of PM2.5 and the chemical compositions showed a decreasing trend with increasing height, while mass percentages of SO4(2-), NO3(-) and OC showed an increasing trend with increasing height. Concentrations of ion species and carbon compound in PM2.5 samples in the daytime were higher than those collected at night, which was due to intense human activities and suitable meteorological condition in the daytime. The ratios of NO3(-)/SO4(2-) and OC/EC were also considered, and we have observed that their levels on heavy pollution days were higher than those on clear days. In addition, source apportionments were identified quantitatively using the CMB-iteration model. The results indicated that contributions of secondary ion species increased with increasing height, while contributions of other pollutant sources decreased, and contributions of vehicle exhaust were relatively high on clear days., (Copyright © 2015 Elsevier B.V. All rights reserved.)

China has witnessed rapid economic growth in the past three decades, especially in coastal areas. Particulate matter (PM) pollution is becoming increasingly serious in China's cities along the western Pacific coast with the rapid development of China's society and economy. This study analyzed PM (PM10 and PM2.5) in terms of their mass and chemical composition in four coastal Chinese cities. The goal was to study the spatial variation and characteristics of PM pollution in sites under different levels of economic development and in diverse natural environments. A distinct trend for concentrations of PM and related chemical species was observed and increased from south to north in Haikou, Ningbo, Qingdao, and Tianjin. Secondary inorganic aerosols, crustal materials, and organic matter dominated the composition of both PM10 and PM2.5. Crustal materials were the most abundant species in the northern coastal areas because these areas have less vegetation cover and lower humidity than southern coastal areas. The presence of high SO4 (2-)/nitrate (NO3 (-)) concentrations indicated that the burning of coals gives significant contributions to PM10 and PM2.5. The differences observed in the characteristics of PM pollution in these coastal cities are probably caused by different levels of industrial and urban development.

The ambient PM(10) and background soil samples were collected and analyzed with ICP-AES in eight cities around China to investigate the levels of ten heavy metals (Ti, V, Cr, Mn, Fe, Co, Ni, Cu, Zn, and Pb). The mean concentrations of ten heavy metals in PM(10) of the eight cities of China followed the order of Zn > Pb > Mn > Cu > Ni > Cr > Co > V. The metals in the ambient PM(10) and soil were compared in each city to evaluate the heavy metal mass fraction from anthropogenic sources in ambient air. The CD values in these cities were all above 0.2, indicating that the ingredients spectrums of PM(10) and soil vary markedly. Most heavy metals were enriched in PM(10), except Fe and Ti. The results showed that almost all the cities suffer important heavy metal pollution from anthropogenic sources. The eight cities were also grouped according to their similarity in heavy metals of ambient PM(10) by cluster analysis to investigate the relationship between the heavy metals and the pollution sources of each city. The conclusion was that the eight cities were divided into three clusters which had similar industrial type and economy scale: the first cluster consisted of Shenzhen, Wuxi, and Guiyang; followed by Jinan and Zhengzhou as the second grouping; and the third group had Taiyuan, Urumqi, and Luoyang.

The vapor-phase and particulate-phase samples were collected from the E-waste dismantling region (E) and a reference region (S), which is located in the upwind direction of the E and where the costume industry is developed. The aim was to acquire information about the concentrations, gas/particle partitioning and distribution of polybrominated diphenyt ethers (PBDEs). 11 congeners PBDEs were detected with GC-NCI-MS. The results showed that E-waste dismantling has resulted in serious pollution and the PBDE concentrations (from tri-to deca-BDE) ranged from 51.1 pg x m(-3) to 2685 pg x m(-3) (mean:830 pg x m(-3)), while the PBDE concentrations (from tri-to deca-BDE) in S were in the range of 1.00 pg x m(-3) to 98.9 pg x m(-3) (mean: 28.7 pg x m(-3)). The gas/particle partitioning of PBDEs exhibited a strong dependence on bromine number. Low-brominated PBDEs tend to have a higher concentration in the gas-phase while highly brominated PBDEs are mostly associated with the particulate. The mass distribution of PBDEs in E (including vapor-phase and particulate-phase) was dominated by penta-BDE, accounting for 54.3% of the total PBDEs, followed by deca-BDE, accounting for 23.8%. This pollution characters validated that the E-waste did not only come from Asia, but also from North America and Europe.

Air samples of total suspended particles (TSP, particles less than 30-60 microm), and particles with aerodynamic diameter smaller than 2.5 microm (PM(2.5)) were collected simultaneously at Guiyu (an electronic waste recycling site), three urban sites in Hong Kong and two urban sites in Guangzhou, South China from 16 August to 17 September 2004. Twenty-two PBDE congeners (BDE-3, -7, -15, -17, -28, -49, -71, -47, -66, -77, -100, -119, -99, -85, -126, -154, -153, -138, -156, -184, -183, -191) in TSP and PM(2.5) were measured. The results showed that the overall average concentrations of TSP and PM(2.5) collected at Guiyu were 124 and 62.1 microg m(-3), respectively. The monthly concentrations of the sum of 22 BDE congeners contained in TSP and PM(2.5) at Guiyu were 21.5 and 16.6 ng m(-3), with 74.5 and 84.3%, contributed by nine congeners (BDE-28, -47, -66, -100, -99, -154, -153, -183 and -191 respectively). This pattern was similar to Tsuen Wan site of Hong Kong. Two urban sites of Guangzhou had the same congener pattern, but were different from Yuen Long and Hok Tsui sites of Hong Kong. The results also showed that the amount of mono to penta brominated congeners, which are more toxic, accounted for 79.4-95.6% of Sigma(22)PBDEs from all sites. All congeners tested in Guiyu were up to 58-691 times higher than the other urban sites and more than 100 times higher than other studies reported elsewhere. The higher concentration in the air was due to heating or opening burning of electronic waste since PBDEs are formed when plastics containing brominated flame retardants are heated.

PM(2.5) was collected at Shanghai urban and suburban sites during spring and autumn. PIXE (Proton Induced X-ray Emission) was used to investigate mass concentration of 15 elements (S, K, Ca, Ti, Cr, Mn, Fe, Ni, Cu, Zn, As, Se, Br, Sr, Pb) in Shanghai PM(2.5). The total mass concentration of the 15 chemical elements was higher in spring (5 038.6 ng x m(-3)) than in summer (3 810.6 ng x m(-3)). In spring, mass concentrations of these elements in urban and suburban samples were in the same level. In summer, concentration of the elements in urban samples were lower than in suburban samples, however, the elements which were originated from anthropogenic resources were in higher level in urban samples. The results of FESEM showed that Shanghai PM(2.5) was consisted of soot aggregates, coal fly ashes, minerals, bio-particles and unidentified particles. The result of Plasmid DNA assay demonstrated bioreactivity of urban PM(2.5) was more reactive than that of suburban PM(2.5), this phenomenon probably was explained by higher mass level of heavy metals and more proportion of soot aggregates in urban PM(2.5).

A method of compound-specific stable carbon isotopic analysis for the research about the sources of atmospheric formaldehyde was preliminary studied using gas chromatography/combustion/isotope ratio mass spectrometry (GC/C/IRMS) via 2, 4-dinitrophenylhydrazine (DNPH) derivatization. In order to evaluate the reproducibility, the accuracy and the carbon isotope effects of the method, formaldehyde with different delta 13C values were used to simulate the sampling procedure. The results show that the maximal analytical deviation for all formaldehyde 2, 4-dinitrophenylhydrazone is 0.3 per thousand and the average deviations between the determined and theoretical delta 13C values of them are 0.24 per thousand +/- 0.14per thousand (ranged from 0.03 per thousand to 0.35 per thousand), less than 0.5 per thousand the technical specifications of the GC/C/IRMS system. These mean that no carbon isotopic fractionation occurred during the procedure. The study for the indoor and outdoor atmospheric formaldehyde in the restaurant show that the stable carbon isotopic compositions are significant different for different sources of formaldehyde. The present method could provide valuable information about the sources of atmospheric formaldehyde.

Seasonal aerosol samples have been collected by Andersen Hi-Vol pumping system equipped with a five stage cascade impactor and a backup filter (size range: 10-7.2 microm, 7.2-3.0 microm, 3.0-1.5 microm, 1.5-0.95 microm, 0.95-0.49 microm,

Size distribution of aerosol samples collected from two urban locations (Liwan and Wushan) and a suburban location (Xinken) in Guangzhou (South China) in autumn using Micro-Orifice Uniform Deposit Impactor (MOUDI) were analyzed for 13 polycyclic aromatic hydrocarbons (PAHs) by gas chromatography with mass selective detection (GC-MS). Bimodal distribution was found for 3- and 4-ring PAHs and unimodal for 5-, 6- and 7-ring PAHs. Different PAH size distribution models were found for urban and suburban. PAHs associated with larger particles in suburban than in urban, and different aging processes of aerosols can account for it. Adsorption behavior may be the main mechanism controlled the size distribution of PAHs in urban, and adsorption, absorption and multilayer adsorption may all play a part in suburban. For the diagnostic ratios of PAHs with the same molecular weight, large differences were found between the range of 1-2.5 microm and 0.1-0.56 microm. The concentrations of 13 PAHs were 39 ng/m3 in Xinken, 71-94 ng/m3 in Wushan and 32-154 ng/m3 in Liwan, and 5-7 ring PAHs were the most abundant.

A novel method has been developed for the compound-specific carbon isotope analysis of atmospheric formaldehyde using gas chromatography/combustion/isotope ratio mass spectrometry (GC/C/IRMS). The method allows the determination of the delta13C value for atmospheric formaldehyde at nanogram levels with higher precision and lower detection limit. In the present work, atmospheric formaldehyde was collected using NaHSO3-coated Sep-Pak silica gel cartridges, washed out by water, then derivatized by cysteamine of known delta13C value, and the delta13C value of its derivative (thiazolidine) determined by GC/C/IRMS. Finally, the delta13C value of atmospheric formaldehyde could be calculated by a simple mass balance equation between formaldehyde, cysteamine, and thiazolidine. Using three formaldehydes with different delta13C values, calibration experiments were carried out over large ranges of formaldehyde concentrations. The carbon isotope analysis method achieved excellent reproducibility and high accuracy. There was no carbon isotopic fractionation throughout the derivatization processes. The differences in the carbon isotopic compositions of thiazolidine between the measured and predicted values were always <0.5 per thousand, within the specifications of the GC/C/IRMS system. The present method was also compared with the previous 2,4-dinitrophenylhydrazine derivatization method, and this method could be performed with lower analytical error and detection limit. Using this method, four 6-h ambient atmospheric formaldehyde samples were consecutively collected from 8 to 9 March 2005. The results showed that the delta13C values of atmospheric formaldehyde were different during the daytime and nighttime. This method proved suitable for the routine operation and may provide additional insight on sources and sinks of atmospheric formaldehyde.

Air samples were collected in June of 2004 from four sites in the city of Guangzhou, a typical urban center in South China, to determine the levels, compositional profiles, and gas-particle distribution of 11 polybrominated diphenyl ether (PBDE) congeners (BDE-28, -47, -66, -100, -99, -85, -154, -153, -138, -183, and -209). The arithmetic mean atmospheric concentrations of sigmaPBDEs (sum of all target PBDE congeners except for BDE-209) in samples from the urban and city background sites were comparable to or slightly higher than those from other places around the world. The arithmetic mean atmospheric concentrations of BDE-209, however, were higherthan those in North America and Europe, and similar to the values from Japan. Congener compositions were dominated by BDE-209 in all (>70%) but an industrial site, with an average abundance of 48% for BDE-209. The PBDE patterns were generally similar to that in the technical penta-BDE mixture, Bromkal 70-5DE. Partitioning of PBDEs between the gas and particle phases (Kp) was well correlated with the subcooled liquid vapor pressure (PLO) for all of the samples, but the relationship differed between samples from different sites. The measured fractions of PBDEs in the particulate phase were compared to the predictions from the Junge-Pankow adsorption and KOA-based absorption models. The results indicated that the KOA-based model worked better than the Junge-Pankow model that tended to overestimate the particulate fractions for most PBDE congeners.