RESUMO
During the summer of 2015, polycyclic aromatic hydrocarbons (PAHs) in the atmosphere were collected by passive air samplers in typical urban-rural fringe of Wuhan-Ezhou region, Central China. The results showed that 16 kinds of PAHs were ubiquitous with the concentrations of ∑16PAHs from 14.69 to 136.30 ng·m-3 and the mean concentration of 43.03 ng·m-3. Phenanthrene (Phe), fluoranthene (Fla) and pyrene (Pyr) were major components, which accounted for 81% of ∑16PAHs. PAHs atmospheric concentrations presented obvious spatial variation, being significantly related to geographical environment and influenced by anthropogenic activity. Air-soil exchange status of PAHs was discussed according to the fugacity fraction (ff). The results showed that HMW-PAHs behaved as net deposition, while LMW-PAHs were more likely to establish dynamic equilibrium between atmosphere and soil than MMW-PAHs and HMW-PAHs. For some PAHs, such as acenaphthylene (Acy) and anthracene (Ant), the soil acted as second sources of them.
Assuntos
Poluentes Atmosféricos/análise , Monitoramento Ambiental , Hidrocarbonetos Policíclicos Aromáticos/análise , Atmosfera , China , Fluorenos , Pirenos , Estações do Ano , Solo , Poluentes do Solo/análiseRESUMO
Atmospheric particulate matters in nine size fractions were sampled at Huangshi city, Hubei province. Elemental concentrations occurred unimodal size distribution for Zn, Pb and Ni, dimodal distribution for Ca, S, Fe and Ti, and trimodal distribution for Cl, K, Mn, Cu and Cr. Enrichment factor and principal component analysis identified the main sources from crustal material, biomass burning, waste incineration, vehicular and industrial emission. As for the non-carcinogenic health risk through inhalation, there were certain potential risks for Mn and Sb for children, and Pb for children and adults in PM2.5. It showed certain potential risks for Mn, Sb and Pb for children and adults in PM10. As for the carcinogenic health risk through inhalation, Cr in PM2.5 and Ni, Co and Cr in PM10 indicated unacceptable risk for children and adults. Meanwhile, Co and Ni in PM2.5 represented acceptable risk for children.
Assuntos
Poluentes Atmosféricos/análise , Monitoramento Ambiental , Material Particulado/análise , Adulto , Biomassa , Carcinógenos/análise , Criança , China , Cidades , Saúde , Humanos , Incineração , Indústrias , Metais Pesados/análise , Análise de Componente Principal , Medição de Risco , Titânio/análise , UrbanizaçãoRESUMO
Aerosol samples of PM2.5 and PM10 were collected every 6 days from March 2012 to February 2013 in Huangshi, a typical industrial city in central China, to investigate the characteristics, relationships, and sources of carbonaceous species. The PM2.5 and PM10 samples were analyzed for organic carbon (OC), elemental carbon (EC), char, and soot using the thermal/optical reflectance (TOR) method following the IMPROVE_A protocol. PM2.5 and PM10 concentrations ranged from 29.37 to 501.43 µg m-3 and from 50.42 to 330.07 µg m-3, with average levels of 104.90 and 151.23 µg m-3, respectively. The 24-h average level of PM2.5 was about three times the US EPA standard of 35 µg m-3, and significantly exceeds the Class II National Air Quality Standard of China of 75 µg m-3. The seasonal cycles of PM mass and OC concentrations were higher during winter than in summer. EC and char concentrations were generally highest during winter but lowest in spring, while higher soot concentrations occurred in summer. This seasonal variation could be attributed to different seasonal meteorological conditions and changes in source contributions. Strong correlations between OC and EC were found for both PM2.5 and PM10 in winter and fall, while char and soot showed a moderate correlation in summer and winter. The average OC/EC ratios were 5.11 and 4.46 for PM2.5 and PM10, respectively, with individual OC/EC ratios nearly always exceeding 2.0. Higher char/soot ratios during the four seasons indicated that coal combustion and biomass burning were the major sources for carbonaceous aerosol in Huangshi. Contrary to expectations, secondary organic carbon (SOC) which is estimated using the EC tracer method exhibited spring maximum and summer minimum, suggesting that photochemical activity is not a leading factor in the formation of secondary organic aerosols in the study area. The contribution of SOC to OC concentration for PM2.5 and PM10 were 47.33 and 45.38%, respectively, implying that SOC was an important component of OC mass. The serious air pollution in haze-fog episode was strongly correlated with the emissions of pollutants from biomass burning and the meteorological conditions.
Assuntos
Poluentes Atmosféricos/análise , Monitoramento Ambiental , Material Particulado/análise , Aerossóis/análise , Poluição do Ar/estatística & dados numéricos , Biomassa , Carbono/análise , China , Cidades , Carvão Mineral , Tamanho da Partícula , Estações do Ano , Fuligem/análiseRESUMO
PM2.5 (particulate matter with an aerodynamic diameter <2.5 µm) samples were collected in Huangshi, central China, from March 2012 to February 2013 and were analyzed for dicarboxylic acids (diacids) and related compounds (DARCs). Oxalic acid (C2; 416 ng m-3) was the most abundant species, followed by phthalic (Ph; 122 ng m-3), terephthalic (tPh; 116 ng m-3), succinic (C4; 70.4 ng m-3), azelaic (C9; 67.9 ng m-3), and adipic (C6; 57.8 ng m-3) acids. Relatively high abundances of Ph and tPh differed from the distribution in urban and marine aerosols, indicating contributions from nearby anthropogenic sources. Glyoxylic acid (ωC2; 41.4 ng m-3) was the dominant oxoacid, followed by 9-oxononanoic (ωC9; 40.8 ng m-3) and pyruvic (Pyr; 24.1 ng m-3) acids. Glyoxal (Gly; 35.5 ng m-3) was the dominant α-dicarbonyl. Highest average concentrations were found for C2, ωC2, and C9 in autumn, for C4, for Pyr and C6 in spring, for Ph, ωC9, and Gly in summer, whereas the lowest values were observed in winter. Seasonal variations and correlation coefficients of DARCs demonstrate that both primary emissions and secondary production are important sources. Principal component analysis of selected DARCs species suggests that a mixing of air masses from anthropogenic and biogenic sources contribute to the Huangshi aerosols. Implications: Both primary emissions and secondary production are important sources of diacids and related compounds in PM2.5 from Huangshi, central China. Principal component analysis of selected diacids in Huangshi aerosols suggests that mixing of air masses from anthropogenic and biogenic sources contribute to ambient aerosols in central China.
Assuntos
Aerossóis/análise , Poluentes Atmosféricos/análise , Ácidos Dicarboxílicos/análise , Material Particulado/análise , China , Monitoramento Ambiental , Análise de Componente Principal , Estações do AnoRESUMO
The surface water and surface sediments were collected from Daye Lake in April 2014. The concentrations of heavy metals were determined by atomic absorption spectroscopy. The pollution potential health risk and ecological risk of heavy metals in water and sediment were assessed by the health risk assessment model and the potential ecological risk index method. The results showed that the concentrations of the heavy metals (Ni, Cd, Cu and Pb) was 49.27 µg·L-1, 2.19 µg·L-1, 12.18 µg·L-1, 12.13 µg·L-1(water) and 78.46 mg·kg-1, 77.13 mg·kg-1, 650.13 mg·kg-1 and 134.22 mg·kg-1 (sediment). Enrichment coefficient indicated that the enrichment of Cd, Cu and Pb was more serious, especially the accumulation of Cd was the most obvious. Compared to typical lakes in China, the contents of heavy metals in water and sediment were relatively high. The spatial pollutant distribution of the heavy metals in water and sediment all presented that the concentrations of the heavy metals were relatively higher in east and west of Daye Lake, relatively more uniform in the middle, and their origins were mainly from human activities. The results of environmental risk indicated that the carcinogens and chemical non-carcinogens health risk values of heavy metals by drinking water pathway were 9.77E-08~1.63E-05a-1. Therefore, the pollution of Ni and Cd should be the primary control target for environmental health risk management. The descending order of pollution degree of four metals in sediment was Cd> Cu> Pb> Ni, and Cd was the main contributor of the potential ecological risk elements.
RESUMO
In order to investigate the characteristics and sources of elements in atmospheric aerosols (PM10) measurements, samples were collected between April 2012 and February 2013 in Huangshi, a typical industrial city in the east of Hubei province, China. These samples were analyzed for seventeen elements using wavelength dispersive X-ray fluorescence spectrometry. In addition, the pollution characteristics of fourteen elements were analyzed by an enrichment factor (EF) method, and the sources of these elements were studied by a principal component analysis (PCA) and positive matrix factorization (PMF) method. The result from the EF indicated that the concentration of the seventeen elements in the PM10 measurements varied from 0.01-9.83 µg·m-3. The elemental concentration of S was the highest and Ni and V was the lowest during the monitoring period in Huangshi. Daily levels of Pb and Cd exceeded the annual reference values set by the National Ambient Air Quality Standard (GB3095-2012) by 36.4% and 89.1%, respectively. An analysis of EF showed that Ti, V, Mn, and Ni elements were mildly enriched, indicating they were affected by both natural and anthropogenic sources. Ca, Cr, and Ba elements were moderately enriched and Cu, Zn, Pb, Sn, Sb, and Fe were highly enriched or hyper accumulated, suggesting they are mainly sourced from human activities. There were four sources significantly contributing to the elements in the PM10measurement, which were determined using PCA and PMF analysis. These were soil and fugitive dust, coal combustion, industry exhausts, and motor vehicle emissions. The results of the two models supported each other and had good consistency.
RESUMO
Bioaerosols of university dormitory can spread through air and cause a potential health risk for student staying in indoor environment. To quantify the characteristics of bioaerosols in indoor environment of university dormitory, concentration and size distribution of culturable bioaerosols were detected during the plum rain period, the correlations of culturable bioaerosol with concentration of particulate matter, the ambient temperature and relative humidity were analyzed using Spearman's correlation coefficient and finally the changes of size distribution of culturable bioaerosol caused by activities of students were detected. The results showed that the mean concentrations of culturable airborne bacteria and fungi were (2133 +/- 1617) CFUm' and (3111 +/- 2202) CFU x m(-3). The concentrations of culturable airborne bacteria and fungi exhibited negative correlation with PM1, PM2.5, and PM10, respectively. The respirable fractions of bacteria exhibited positive correlation with PM2.5, and the respirable fractions of fungi exhibited significant positive correlation with PM10. Ambient temperature had positive correlation with culturable airborne bacteria and fungi, and relative humidity had negative correlation with culturable airborne bacteria and fungi. In the afternoon, concentrations of culturable airborne fungi in indoor environment of university dormitory significantly increased, and the size distribution of culturable hioaerosols was different in the morning and afternoon.