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1.
The present paper reports chemistry and fluxes of dust-carbon mixed coarse particles. For the purpose of this study, different carbonaceous fractions i.e. organic carbon ((OC), elemental carbon (EC) and carbonate carbon (CC) of atmospheric dust and their respective local soils were quantified at three sites of National Capital Region (NCR) of Delhi viz. Jawaharlal Nehru University campus (JNU), Connaught Place (CP) and Vishali area of Ghaziabad (GB). It has been observed that the OC and EC levels were approximately five to nine times higher in urban atmospheric dust than their corresponding soils, whereas CC levels were about three times higher than the corresponding soils. Average dustfall fluxes were significantly different at all the sites due to their different land-use patterns. At urban background site (JNU), the dust flux was lowest (172 mg/m2/day) followed by CP, a commercial site, (192 mg/m2/day) and GB, an industrial/residential area, (302 mg/m2/day). Similar to the dustfall pattern, the mean values of OC, EC and CC deposition fluxes were also observed to be lowest at JNU (9.2, 0.8 and 1.0 mg/m2/day, respectively) as compared to CP (12.2, 1.2 and 1.3 mg/m2/day, respectively) and GB sites (11.1, 1.1 and 1.4 mg/m2/day, respectively). Interestingly, unlike fine mode, different correlation pattern of OC and EC in coarse mode dust aerosols at three sites has suggested their independent deposition processes and source contribution. Fluxes of major water soluble inorganic ions (Na+, NH4 +, K+, Ca2+, Mg2+, F?, Cl?, NO3 ? and SO4 2?) were also determined. Ca2+, Cl? and SO4 2? were found to be the major ionic species of water soluble fraction of the urban dust at all the sites. These interactions are corroborated by the morphology of the mixed aerosols. High levels of measured chemical species and their spatial distribution revealed close correspondence with the local emissions from transport, industries, biomass burning, road dust and construction activities etc.  相似文献   

2.
北京乡村地区分粒径气溶胶OC及EC分析   总被引：2，自引：0，他引：2       下载免费PDF全文
利用北京上甸子区域大气本底站2004年观测的分粒径大气气溶胶资料,分析了气溶胶中有机碳 (OC) 及元素碳 (EC) 的质量浓度水平、季节变化、尺度分布特征、OC与EC比值及其相关性。结果显示:上甸子站总悬浮颗粒物 (TSP) 中OC平均质量浓度为7.5~31.5 μg·m-3,EC质量浓度为1.4~6.6 μg·m-3;PM2.1(粒径小于2.1 μm) 中OC质量浓度为4.0~19.1 μg·m-3,EC质量浓度大约为0.8~4.3 μg·m-3。冬季OC及EC质量浓度明显高于其他季节,其中冬、夏、秋季OC及EC峰值粒径出现为0.65~2.1 μm,但在春季峰值粒径移至2.1~4.7 μm。观测期间,OC与EC质量浓度比值平均为4~6,该比值略高于文献报道的我国一些城市地区的观测结果。  相似文献   

3.
Size distribution aerosol samples collected at two urban locations (Liwan and Wushan) and a suburban location (Xinken) in Guangzhou (South China) in autumn using a MOUDI (Micro-orifice Uniform Deposit Impactor) have been analyzed for 13 polycyclic aromatic hydrocarbons (PAHs) by gas chromatography with mass selective detection (GC-MS). Different PAH size distribution models were found for urban locations and a suburban location. The particle size distributions of PAHs tend to shift toward a larger size in a suburban location than in an urban location caused by aerosol aging processes. The ratios of total-PAH/TSP changed greatly during different sampling periods, even though the samplings were conducted consecutively. This can be the result of reactions between PAHs and atmospheric photooxidants, and the formation of SOAs (secondary organic aerosols) during the aging process. Adsorption behavior on available aerosol surface area, absorption behavior in available aerosol organic mass and multilayer adsorptive accumulation in coarse mode aerosols were the three mechanisms which control the size distribution of PAHs.  相似文献   

4.
Aerosol mass size distribution has been measured by using an optical particle counter. The measurements were done in an urban background location in the western Mediterranean during winter 2006. The study has been focused in determining the mass size distribution under special meteorological conditions like moderate rain, considerable winds and high atmospheric stability. The results obtained showed a mass predominance of accumulation mode during rain and high stability periods although for different reasons. In the case of rain, it is due to greater atmospheric cleansing effectiveness that rain has upon coarse mode particles. However, during stagnant periods, the meteorological situation favored coagulation processes among nucleation mode particles giving like result a mass increase in the accumulation mode. Finally, strong winds favor the resuspension of the largest particles and the dispersion of particles with sizes inferior to 7.5 μm. Similar results have been reproduced using principal component analysis (PCA). In this way, three components were identified. The first (PC1) represents particles in the accumulation mode. The second component (PC2) is constituted by coarse particles to 7.5 μm, and the third (PC3) corresponds to coarser particles. The contribution of each group to the overall average concentration was determined: 27.2% corresponds to particles with sizes belonging within the first component, 35.4% to PC2 and 37.3% to PC3. Important percentage variability for each component under meteorological episodes has been obtained. Results obtained showed an important increase of PC1 during Rainy Days (53.8%) and High Pollution Days (40.2%). Contrary to this on Windy Days this component decreases to 7.4%. However, during this kind of day PC3 increases to 64.6%.  相似文献   

5.
太原冬季PM2.5中有机碳和元素碳的变化特征   总被引：4，自引：2，他引：4       下载免费PDF全文
2005年12月—2006年2月在太原市区持续观测了气溶胶细粒子PM2.5, 并应用Sunset碳分析仪进行了有机碳 (organic carbon, OC) 和元素碳 (elemental carbon, EC) 的测定。结果表明:太原冬季PM2.5, OC和EC浓度均较高, 其中PM2.5日平均浓度变化范围为25.4~419.0 μg/m3, 日平均浓度为193.4±102.3 μg/m3, OC平均浓度为28.9±14.8 μg/m3, EC平均浓度为4.8±2.2 μg/m3, OC/EC平均比值是7.0±3.9, 即太原市冬季PM2.5和碳气溶胶污染严重。OC在PM 2.5中占18.6%, EC占2.9%, 这表明碳气溶胶是太原大气细粒子污染控制的关键组分。在太原市冬季, 采暖燃烧的煤是OC和EC的主要贡献源, 造成OC大大高于EC, 从而使OC/EC比值增大。各种气象条件对PM2.5, OC, EC和OC/EC比值的变化都有不同程度的影响, 特别是大雾天气、相对湿度、风速和降雪是影响碳气溶胶浓度变化的重要因素。  相似文献   

6.
Ambient concentrations of organic carbon (OC), elemental carbon (EC) and water soluble inorganic ionic components (WSIC) of PM10 were studied at Giridih, Jharkhand, a sub-urban site near the Indo Gangatic Plain (IGP) of India during two consecutive winter seasons (November 2011–February 2012 and November 2012–February 2013). The abundance of carbonaceous and water soluble inorganic species of PM10 was recorded at the study site of Giridih. During winter 2011–12, the average concentrations of PM10, OC, EC and WSIC were 180.2?±?46.4; 37.2?±?6.2; 15.2?±?5.4 and 18.0?±?5.1 μg m?3, respectively. Similar concentrations of PM10, OC, EC and WSIC were also recorded during winter 2012–13. In the present case, a positive linear trend is observed between OC and EC at sampling site of Giridih indicates the coal burning, as well as dispersed coal powder and vehicular emissions may be the source of carbonaceous aerosols. The principal components analysis (PCA) also identifies the contribution of coal burning? +?soil dust, vehicular emissions?+?biomass burning and seconday aerosol to PM10 mass concentration at the study site. Backward trajectoy and potential source contributing function (PSCF) analysis indicated that the aerosols being transported to Giridih from upwind IGP (Punjab, Haryana, Uttar Pradesh and Bihar) and surrounding region.  相似文献   

7.
Particle number and mass concentrations were measured in Beijing during the winter and summer periods in 2003, together with some other parameters including black carbon (BC) and meteorological conditions. Particle mass concentrations exhibited low seasonality, and the ratio of PM2.5/PM10 in winter was higher than that in summer. Particle number size distribution (PSD) was characterized by four modes and exhibited low seasonality. BC was well correlated with the number and mass concentrations of accumulation and coarse particles, indicating these size particles are related to anthropogenic activities.Particle mass and number concentrations (except ultra-fine and nucleation particles) followed well the trends of 13C concentration for the majority of the day, indicating that most particles were associated with primary emissions. The diurnal number distributions of accumulation and coarse mode particles were characterized by two peaks.  相似文献   

8.
Particle-associated polycyclic aromatic hydrocarbons (PAHs) in outflow from East Asia were observed at Cape Hedo, Okinawa, Japan between 2005 and 2008. The filter samples of the total suspended particles were analyzed by means of gas chromatography-mass spectrometry. The total concentration of fourteen 3–7-ring PAHs was 0.01–24 ng m?3 (average 1.6 ng m?3). The average PAH concentration increased in the winter-spring season and decreased in the summer-fall season. The average benzo(a)pyrene to benzo(e)pyrene ratio was 0.49 in the winter-spring season and was lower than the literature values for East Asian cities in the same season. This result shows that aging of organic aerosol particles proceeds during long-range transport from East Asia. In the Asian Pacific region, these pollutants are transported from East Asia in the winter-spring season, whereas clean air mass is transported from the Pacific Ocean in the summer-fall season.  相似文献   

9.
Polycyclic aromatic hydrocarbons (PAHs) are ubiquitous pollutants in the urban atmosphere. An investigation on seasonal variation of PAHs in the urban atmosphere of Guangzhou, China was conducted in this study. 112 PM10 (particulate matter with aerodynamic diameter < 10 μm) samples were collected at two sites between June 2002 and June 2003. PAHs were analyzed with GC–MS (gas chromatography–mass spectrometry). The result showed that PAHs exhibit distinct seasonal variation. The seasonal concentration for the ∑PAHs ranged from 8.11 to 106.26 ng m− 3. The average ∑PAHs measured were highest in winter and lowest in summer. The PAHs distribution patterns were similar within each season at two sites. 5–6 ring PAHs were the abundant compounds, which accounted for 65–90% of ∑PAHs and benzo [b + k] fluoranthene dominated in four seasons. The PAHs concentration and distribution pattern fluctuated greatly in winter for the cold air current. Based on the different temperature in winter, the samples were split into two groups. PM10 and the abundance of the PAHs in winter-1 (temperature, 12–22 °C) were much greater than in winter-2 (temperature, 8–12 °C). In winter-1 benzo [b + k] fluoranthene and Indeno [1, 2, 3] pyrene dominated while chrysene and benzo [b + k] fluoranthene dominated in winter-2. Meteorological conditions such as wind speed and temperature had a strong influence on the seasonal variation. Potential sources of PAHs were identified using the molecular diagnostic ratios between PAHs. Results showed fossil fuel combustion may be the major source of PAHs at the two sites.  相似文献   

10.
Particle number size distribution(PNSD) between 10 nm and 20 μm were measured in the Pearl River Delta(PRD) region in winter 2011.The average particle number concentration of the nucleation mode(10-20 nm),Aitken mode(20-100 nm),accumulation mode(100 nm-1μm) and coarse mode(1-20 μm) particles were 1 552,7 470,4 012,and 19 cm-3,respectively.The volume concentration of accumulation mode particles with peak at 300 nm accounted for over 70% of the total volume concentration.Diurnal variations and dependencies on meteorological parameters of PNSD were investigated.The diurnal variation of nucleation mode particles was mainly influenced by new particle formation events,while the diurnal variation of Aitken mode particles correlated to the traffic emission and the growth process of nucleation mode particles.When the PRD region was controlled by a cold high pressure,conditions of low relative humidity,high wind speed and strong radiation are favorable for the occurrence of new particle formation(NPF) events.The frequency of occurrence of NPF events was 21.3% during the whole measurement period.Parameters describing NPF events,including growth rate(GR) and source rate of condensable vapor(Q),were slightly larger than those in previous literature.This suggests that intense photochemical and biological activities may be the source of condensable vapor for particle growth,even during winter in the PRD.  相似文献   

11.
Sampling of particulate matter with aerodynamic diameter cut off at 2.5 μm (PM2.5) has been carried out over a semi urban site of Pune and an urban site of Hyderabad. Analysis of elemental Carbon (EC) and Organic Carbon (OC) present in PM2.5 was carried out using advanced Desert Research Institute’s (DRI) Thermal/Optical Carbon Analyzer operated on IMPROVE_ A (Interagency Monitoring of Protected Visual Environments_ A) protocol. It is found that average concentration of EC and OC both at Pune and Hyderabad was highest during winter season and lowest during monsoon season. Winter high is mainly controlled by inversion, whereas monsoon low is due to rain-out and wash-out process. OC/EC ratio showed higher variation over Pune compared to that over Hyderabad in different seasons, indicating divergent sources of emission of OC and EC at Pune. Formation of Secondary Organic Carbon (SOC) has also been identified as one of the reasons for wide variation in OC/EC ratio value in different seasons over both the sites.  相似文献   

12.
The indoor PM2.5 aerosol samples for charcoal broiling source under Chinese traditional charbroiling and the ambient fine aerosols samples (PM2.5) were collected in Beijing to investigate the characteristics of the charcoal broiling source and its impact on the fine organic aerosols in the atmosphere. The concentrations of 20 species of the trace organic compounds, including polycyclic aromatic hydrocarbons (PAHs), fatty acids, levoglucosan, and cholesterol in PM2.5 were identified and quantified by GC/MS. The total PAHs and fatty acids emitted from charcoal broiling to PM2.5 were 8.97 and 87,000 ng mg−1 respectively. The concentrations of the light molecular weight (LMW) 3- and 4-ring PAHs were much higher than those of the high molecular weight (HMW) 5- and 6-ring PAHs. Fatty acids were the most abundant species in source profile, accounting for over 90% of all identified organic compounds. More polyunsaturated fatty acid (linoleic acids) than the saturated fatty acid (stearic acids) emitted in the cooking. Charcoal broiling is a minor source of PAHs compared to the source of biomass burning. Comparing the ratios of levoglucosan/fatty acid and levoglucosan/cholesterol in the charcoal broiling samples to the ambient samples, it is evident that meat cooking is an important source of fatty acids, but a less important source of cholesterol. Cooking, as one of the source of fine organic particles, plus other anthropogenic sources would be related to the formation of the severe haze occurred and spread over the urban atmosphere in most of the cities of China in the past several years.  相似文献   

13.
Emissions of Polycyclic aromatic hydrocarbons by savanna fires   总被引：2，自引：0，他引：2  
Although Polycyclic aromatic hydrocarbons (PAH) are known as anthropogenic compounds arising from the combustion or the pyrolysis of fossil fuels, they may be also emitted by the combustion of vegetation. A field study was carried out in January 1991 at Lamto (Ivory Coast) as part of the FOS DECAFE experiment (Fire Of Savanna). Some ground samplings were devoted to the qualitative and quantitative characterization of atmospheric emissions by savanna fires during prescribed burns and under background conditions. Specific collections for gaseous and particulate PAHs have shown that the African practice of burning the savanna biomass during the winter months is an important source of PAHs. These compounds are emitted mainly in gaseous form but a significant fraction, essentially heavy PAHs, is associated with fine carbonaceous particles and can therefore represent a hazard for human health, since some of these compounds are mutagenic and carcinogenic. Twelve compounds were identified during the fire episodes and in the atmospheric background. The total concentration in the fires is of the order of 10 ng m–3 for the gas phase and from 0.1 to 1 ng m–3 in the aerosols. In the atmospheric background the mean concentrations are regular, 0.15 ng m–3 and 2 pg m–3, respectively. These concentrations are comparable with what is observed in European rural zones. The particulate emissions of PAHs by the savanna fires are distinguished by the abundance of some compounds which can be considered as tracers, although they are also slightly emitted by fossil fuel sources. These compounds are essentially pyrene, chrysene and coronene. In the gas phase, although no individual PAH may be considered as specific of the biomass combustion emissions, the relative abundances of the main PAHs are characteristic of the biomass burning. The concentrations of pyrene and fluorene are always predominant; these compounds could be considered as characteristic emission products of smoldering and flaming episodes, respectively. In the background the PAH composition shows that in a tropical region the air consists of a mixture coming from the various sources, but the biomass combustion is by far the most important source.The fluxes of total PAH emitted by savanna biomass burning in Africa were estimated to be of the order of 17 and 600 ton yr–1, respectively, for the particulate PAHs and the gaseous PAHs, respectively.  相似文献   

14.
Fine aerosol samples were collected throughout spring, summer, and winter in 2004∼2005 at a major urban traffic junction (BNU) and a suburban location (MY) in Beijing and at a downtown site (SH) in Shanghai, China. Ten of the 16 EPA priority polycyclic aromatic hydrocarbons (PAHs), seven fatty acids, levoglucosan, and cholesterol were identified and quantified. PAHs detected in Beijing and Shanghai were up to one order of magnitude higher than those reported in the developed countries either in urban or suburban areas, while levoglucosan was one order of magnitude lower than that in other countries for no biomass combustion in domestic heating in the mega-cities in China. PAHs showed the same seasonal trend in all sampling sites as the highest in winter and the lowest in summer, while fatty acids no pronounced seasonal variation. A significant fraction of levoglucosan from cooking with higher concentrations in urban than in suburban area contributed to the ambient atmosphere, indicating that the main source of levoglucosan in urban environment would be cooking rather than biomass burning. The relative contributions of coal combustion and vehicle exhaust sources to PAHs in fine aerosols were preliminarily estimated to be 1:2 in Beijing and 1:1 in Shanghai, revealing that the air pollution in these mega-cities in China was mainly the mixing of coal combustion with vehicle exhaust. Cooking was one of the major sources of organic aerosols in both Beijing and Shanghai.  相似文献   

15.
Ambient concentrations of polycyclic aromatic hydrocarbons (PAHs) were measured in Helsinki (Finland). Particle mass size distributions were obtained with a cascade impactor (12 stages) with glass fibre filters as substrates. Simultaneously with the impactor measurements, particulate and gaseous PAHs were collected on a quartz filter and XAD-2 adsorbent, respectively, for evaluation of gas-partition coefficients. Samples were analysed for PAHs by on-line coupled supercritical fluid extraction — liquid chromatography — gas chromatography — mass spectrometry. The impactor results showed that most of the PAHs in Helsinki urban area were concentrated in fine particles (<2.5 μm diameter) with unimode peak at about 1 μm. The results were comparable with the number distribution measured with a differential mobility particle sizer. Total amounts of PAHs (gas + particle) varied from 15 (acenaphthylene) to 1990 (fluorene) pg/m3. The PAHs lighter than 202 amu (pyrene and fluoranthene) were exclusively in gas phase, whereas those heavier than 202 amu were mostly associated with particles. A plot of the partition coefficients (logKp) versus the temperature dependent sub-cooled vapour pressures (logp L 0 ) showed a gradient of −0.66, which deviated from equilibrium state (gradient = −1).  相似文献   

16.
华北平原是我国主要农作物产区,田间秸秆焚烧现象普遍存在,选取秋收季节（2014年10月）分析了秸秆燃烧的排放特征,利用区域化学传输模型WRF-Chem模拟研究了燃烧排放对气态前体物及其氧化产物的影响,以及最终导致的PM2.5中硫酸盐、硝酸盐和铵盐的变化。研究表明:2014年秋收季节,河南和山东等省份的秸秆燃烧排放会在东南风的输送作用下影响京津冀地区;秸秆燃烧排放大量挥发性有机物（VOCs）,导致火点源及周边地区大气中主要氧化剂浓度上升,提升了区域大气氧化能力;当携带大量VOCs的秸秆燃烧烟羽与以化石燃料排放为主的城市气团相混合时,大气氧化性增强会加速城市地区人为源排放的NOx和SO2等气态前体物的氧化过程,提高硫酸盐和硝酸盐的形成速率、促进二次无机气溶胶的生成。  相似文献   

17.
Chemical characteristics of haze during summer and winter in Guangzhou   总被引：33，自引：0，他引：33  
Airborne particles were collected with a 10-stage MOUDI and a PM10 sampler in Guangzhou, China, during both haze and normal days in the summer of 2002 and 2003, and winter 2002. The characteristics of PAHs, organic carbon, elemental carbon and water-soluble inorganic ions were studied under four periods (summer normal, summer haze, winter normal and winter haze). In this study, secondary pollutants (OC, SO42−, NO3− and NH4+) were the major chemical components and appeared to show a remarkably rapid increase from normal to haze days. The particle mass size distributions were bimodal and dominated by fine particles in haze days. A significantly higher OC/EC ratio was found in haze days (3.2–4.7) compared to normal days (1.8–2.8), indicating secondary organic aerosol formation might be significant during haze days. Correlation analysis between visibility and chemical species showed that the major scattering species were TC (total carbon) and sulfate in normal days and nitrate and TC in haze days, respectively. Simultaneously, correlation analysis between visibility and meteorological factors demonstrated that visibility increased with both temperature and wind speed, while it decreased with relative humidity. Furthermore, the relatively higher value of IcdP/(BghiP + IcdP) and the low value of Cmax, CPI, and BghiP/BeP in winter haze could be due to the growth of motor vehicle usage and energy consumption in winter.  相似文献   

18.
A high-volume cascade impactor, equipped with a PM10 inlet, was used to collect size-segregated aerosol samples during the summer of 2004 at two Portuguese locations: a coastal-rural area (Moitinhos) and an urban area (Oporto). Concentrations of airborne particulate matter (PM), total carbon (TC), organic carbon (OC), elemental carbon (EC), and water-soluble organic carbon (WSOC) were determined for the following particle size ranges: < 0.49, 0.49–0.95, 0.95–3.0, and 3.0–10 µm. The total PM mass concentrations at the urban and coastal-rural sites ranged from 22.8 to 79.6 μg m− 3 and 19.9 to 28.2 μg m− 3, respectively, and more than 56% of the total aerosol mass was found in the fractions below 3.0 μm. At both locations the highest concentrations of OC and EC were found in the submicrometer size range. The regional variability for the OC and EC concentrations, with the highest concentrations being found in the urban area, was related to the contribution of local primary sources (mostly traffic emissions). It was also verified an enrichment of the small size particles in WSOC, representing on average 37.3(± 12.4)% and 59.7(± 18.0)% of OC in the very fine aerosol at the coastal-rural and urban areas, respectively. The amount of secondary OC calculated by the minimum OC/EC ratio method indicates that secondary organic aerosol formation was important throughout the study at both sites. The obtained results suggest that long-range transport and favourable summer conditions for photochemical oxidation are key factors determining secondary OC formation in the coastal-rural and urban areas. The ultraviolet absorption properties of the chromophoric constituents of the WSOC fractions were also different among the different particle size ranges and also between the two sampling locations, thus suggesting the strong impact of the diverse emission sources into the composition of the size-segregated organic aerosol.  相似文献   

19.
《Atmospheric Research》2009,91(2-4):253-263
A high-volume cascade impactor, equipped with a PM10 inlet, was used to collect size-segregated aerosol samples during the summer of 2004 at two Portuguese locations: a coastal-rural area (Moitinhos) and an urban area (Oporto). Concentrations of airborne particulate matter (PM), total carbon (TC), organic carbon (OC), elemental carbon (EC), and water-soluble organic carbon (WSOC) were determined for the following particle size ranges: < 0.49, 0.49–0.95, 0.95–3.0, and 3.0–10 µm. The total PM mass concentrations at the urban and coastal-rural sites ranged from 22.8 to 79.6 μg m− 3 and 19.9 to 28.2 μg m− 3, respectively, and more than 56% of the total aerosol mass was found in the fractions below 3.0 μm. At both locations the highest concentrations of OC and EC were found in the submicrometer size range. The regional variability for the OC and EC concentrations, with the highest concentrations being found in the urban area, was related to the contribution of local primary sources (mostly traffic emissions). It was also verified an enrichment of the small size particles in WSOC, representing on average 37.3(± 12.4)% and 59.7(± 18.0)% of OC in the very fine aerosol at the coastal-rural and urban areas, respectively. The amount of secondary OC calculated by the minimum OC/EC ratio method indicates that secondary organic aerosol formation was important throughout the study at both sites. The obtained results suggest that long-range transport and favourable summer conditions for photochemical oxidation are key factors determining secondary OC formation in the coastal-rural and urban areas. The ultraviolet absorption properties of the chromophoric constituents of the WSOC fractions were also different among the different particle size ranges and also between the two sampling locations, thus suggesting the strong impact of the diverse emission sources into the composition of the size-segregated organic aerosol.  相似文献   

20.
南京市大气细颗粒物化学成分分析   总被引：20，自引：3，他引：17  
为了解南京大气细粒子的污染水平和污染特征,在南京市中心鼓楼和北郊南京信息工程大学校内进行了连续1a、每季度5d的大气气溶胶同步采样。用称重法、离子色谱法和电感耦合等离子质谱法分别测得细颗粒物的质量浓度、水溶性离子和元素组成。结果表明,南京地区PM2.1污染比较严重,水溶性离子是细粒子的重要组分,所测6种离子质量浓度总和分别占市区和北郊PM2.1的46.99％、42.32％。PM2.1中的各离子最高浓度都出现在冬季。NH^＋4与SO^2-4的相关性好,可能主要以（NH4）2SO4形式存在。温度对SOR和NOR的影响显著,温度升高时SOR值增大而NOR显著减小。通过计算NO^-3与SO^2-4的质量比发现,南京市SO2和NOx主要来自于固定源（如煤的燃烧）。分析细颗粒物中元素含量和富集因子结果表明,Pb、As、Zn、Hg、Cu、Cr、Ni元素的人为污染较明显,且北郊的污染重于市区。比较PM2.1和PM3.3中的离子成分发现,SO^2-4、NH^＋4在PM2.1中占据绝对优势,F^-、Cl^-、NO^-2、NO^-3等不在细粒子中占明显优势。从元素组成来看,Pb、Zn在PM2.1细粒子中含量显著,而Ca、Mg、Na等在粗粒子中富集。  相似文献   

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