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1.
Atmospheric aerosol samples collected in Beijing during 17-21 September 2004 were analyzed using the proton-induced X-ray emissions (PIXE) method, yielding concentrations of 20 elements. Analyzing the aerosol element size-spectrum distribution, enrichment factor (EF) and source over Beijing showed that under strong wind weather conditions, there were double peak distributions in the element size-spectra of Cu, S, K, Mn, As, Br, and Pb: one in fine mode and another in coarse mode. The peak in fine mode resulted from local emissions related to human activities, while the peak in coarse mode was caused by long range transport. The EF values of elements Ni, Cu, Zn, As, Se, Br, and Pb were relatively high, suggesting an evident characteristic polluted by regional aerosol. Results from factor analysis indicated that soil dust, coal-burning, industry and vehicle emissions contributed considerably to the autumn aerosol pollution in Beijing.  相似文献   

2.
Vertical profiles of fine and coarse aerosol particles were determined by cascade impactors at the me-teorological tower in Beijing for three days and one night, July 18-23, 1980. Coarse mode aerosols showed a maximum concentration at 47 m when there was an inversion at about 140 m height, and a rather uniform distribution when there was no inversion. This may indicate a two-component origin of coarse particles at the tower site, one being surface dust and the other being tall stack emissions. Fine mode aerosols showed more complex vertical profiles. Median particle size distributions of most metals were bimodal, indicating distinct coarse particle dispersion and fine accumulation mode processes. A chemical thermodynamic cal-culation indicates that fine mode Si can result from the reduction of silica to volatile SiO during coal combustion with limited air supply, a process which should release substantial amounts of carbon monoxide to the atmosphere.  相似文献   

3.
西太平洋气溶胶微量元素的初步研究   总被引：5，自引：0，他引：5  
本文根据TOGA计划第二航次中采集的气溶胶样品对西太平洋气溶胶的微量元素进行了初步研究。结果表明,海洋气溶胶中Si,Fe,Mn,Ti等地壳元素以及Cu,Zn等一些重金属元素的浓度较陆地相对清洁区气溶胶低。但在近大陆海洋气溶胶中Cu,Fe,K,Si,S等元素的含量相对较高。在调查的海域内气溶胶微量元素的浓度呈现出地理位置和季节上的变化。  相似文献   

4.
Size-segregated aerosol samples were collected with a low-pressure impactor (LPI) at urban, roadside and rural sites in winter in Beijing. The size distribution of Polycyclic Aromatic Hydrocarbons (PAHs), organic carbon (OC) and elemental carbon (EC) were measured and this study focused on their size distributions and relationships of PAH to OC/EC. All PAHs show uni-modal at the accumulation mode (0.1–1.8 μm) and almost all PAHs are associated with fine particles. The absence of PAHs in the nucleus mode contributes to the coagulation under the condition of high concentration of the accumulation mode particles. The absence of PAHs in the coarse mode was probably attributed to the low temperature that restrained the redistribution of PAHs from the accumulation mode to the coarse mode. Flu(fluoranthene) and Pyr(pyrene, 4-ring) were the most abundant particulate PAHs ; however, IcdP(indeno[1,2,3-cd]pyrene) and BghiP(benzo[ghi]perylene, 6-ring) were rather low. Diagnostic ratios show vehicle and coal burning were the major sources of PAHs in winter. Ratios at rural site are obviously different from those found at roadside and urban sites. Lower value of OC/EC in the rural area than that in the urban area was probably resulted from coal burning prevailed in the rural area. OC1 and OC2 exhibit uni-mode distribution similar to their particle surface area distribution indicating their existence on particles by adsorption. OC3 and OC4 show bi-mode distribution. Grinding of biomass debris can be a probable source of OC3 and OC4 in the coarse mode. EC1 is mostly from the pyrolysis of OC; however, both the natural and anthropogenic emissions contribute to EC2. The correlation between size-segregated PAHs and carbonaceous component is also discussed to identify their sources.  相似文献   

5.
Research flights in November 1990 over the central parts of the United States, Wyoming and Colorado, were aimed to the investigation of the properties and microstructure of cirrus clouds (mainly cirrocumulus lenticularis). Among the other parameters measured on board the NCAR Saberliner were the concentration and size distribution of submicron particles and, in some cases, the particle deliquescence. For coarse insoluble particles found inside and outside of cloud elements, size distributions and morphology information were obtained by evaluating inertial impactor samples with an optical microscope and scanning electron microscope. In addition, the coarse particle composition was determined by x-ray energy spectrum analysis. The following conclusions from these measurements are:The large and coarse particle size distribution can be roughly simulated by a log-normal function with the modus around r=0.5 μm. Particle concentrations are very variable between several tenths and several particles per cm3. Particle volume distribution features a distinct maximum around 0.75 μm without a broad plateau which was observed in the case of sampling at lower altitude. Aerosol composition heterogeneity at cirrus cloud level is well documented by the evaluation of the fine particle sampling taken with the UMR sampling system. This heterogeneity can be partly explained by the interaction between aerosol and cloud elements, which is documented by the measured particle size distribution curves inside and outside of cloud elements. Assuming that particle deliquescence is caused by H2SO4 and/or by (NH4)2SO4, particle soluble mass fractions were found to be around 30% in the first case and about 40% in the second. The most frequently occurring elements in large and coarse particles at cirrus cloud level were Si, Cl, Ba, S, Ca and C.  相似文献   

6.
Characterization of aerosols is required to reduce uncertainties in satellite retrievals of global aerosols and for modeling the effects of these aerosols on climate.Aerosols in the North China Plain(NCP) are complex,which provides a good opportunity to study key aerosol optical properties for various aerosol types.A cluster analysis of key optical properties obtained from Aerosol Robotic Network(AERONET) data in Beijing and Xianghe during 2001-11 was performed to identify dominant aerosol types and their associated optical properties.Five dominant aerosol types were identified.The results show that the urban/industrial aerosol of moderate absorption was dominant in the region and that this type varied little with season.Urban/industrial aerosol of weak absorption was the next most common type and mainly occurs in summer,followed by that strong aerosols occurring mainly in winter.All were predominantly fine mode particles.Mineral dust(MD) and polluted dust(PD) occurred mainly in spring,followed by winter,and their absorption decreased with wavelength.In addition,aerosol dynamics and optical parameters such as refractive index and asymmetry factor were examined.Results show that the size of coarse mode particles decreased with AOD indicating the domination of external mixing between aerosols.  相似文献   

7.
南京北郊冬季大气气溶胶及其湿清除特征研究   总被引：18，自引：0，他引：18  
利用WPS(宽范围颗粒粒径谱仪)、雨滴潜仪和雾滴谱仪测量了2007～2008年冬季南京北郊大气气溶胶数浓度谱分布和降水强度,分析了气溶胶粒子的分布特征以及气溶胶粒径与湿清除系数的关系.结果表明:气溶胶粒子具有明显的双峰型R变化特征,数浓度主要集中在0.02～O.2μm粒径范围内,受汽车尾气排放、混合层高度变化以及颗粒物水平输送的影响较大.降雨、降雪和雾过程都对气溶胶粒子有不同程度的清除,降雨和浓雾对核模态和粗模态的气溶胶粒子的清除能力显著,降雪对粒径小于0.03μm的气溶胶粒子的清除能力较强.  相似文献   

8.
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   

9.
In the framework of the 2nd Aerosol Characterization Experiment (ACE-2), in June and July 1997, size segregated samples were collected for single particle analysis on the island of Tenerife, in both the marine boundary layer (MBL) and the free troposphere (FT), to study the characteristics of the North Atlantic aerosol. A systematic assessment was made of the aerosol under background conditions and when the environment was perturbed by European emissions and/or Saharan dust. The aerosol particles were analysed by automated and manual SEM-EDX, followed by cluster analysis to identify the different particle types and their abundance. Basing on back trajectory calculations, particle numbers and volume concentrations, different periods can be identified regarding the origin of the sampled air masses. In the FT, the air masses were classified as clean Atlantic, Saharan dust from Africa or pollution from Europe. In the MBL, air masses were classified as clean, polluted or perturbed by emissions from Europe. For both the FT and MBL samples, the main changes in chemical composition were observed between the fine and coarse mode aerosol. The FT fine mode aerosol is dominated by S-poor aluminosilicates (62%) in the event of the dust samples or sulphates, carbonaceous particles (20%) and S-rich aluminosilicates (46%) in the polluted samples. For the larger fractions, a strong decreasing trend was observed for the sulphates (less than 20%) and carbonaceous particles (10%) in the polluted samples. The MBL fine mode was completely dominated by S-rich particles (polluted 55% and perturbed 59%), and to a lesser extent, carbonaceous and aged sea salt particles. In the coarse mode, the polluted air mass is dominated by sea salt particles (62%). Contrary to the fine fraction, the polluted air mass in the coarse fraction contained 5.3% of S-rich particles. The combined interpretation of the data from the analysis of size-fractioned particles and the calculated backward trajectories for air masses coming from Europe, Africa and the Atlantic, results in better insights on aerosol chemistry, especially for the comparison of the particle composition in the FT and the MBL.  相似文献   

10.
The insular suburban site of Castillo de Bellver was selected for the study of the variability of PM levels and composition in the Western Mediterranean Basin (WMB).Mean annual (in 2004) PM10 and PM2.5 levels at this site were 29 and 20 µg/m3, respectively. These levels may be regarded as relatively low when compared with other suburban insular locations in the Eastern Mediterranean Basin (EMB), but they are higher than those recorded at most of the European suburban sites, especially in Northern and Western Europe. Seasonal variability of PM levels at this site is governed by meteorology rather than local emissions, whereas the daily cycles are clearly defined by the anthropogenic emissions, mainly coming from the urban area of Palma de Mallorca and the harbour area of the same city.Concerning the aerosol composition at this site, the main PM constituent is the mineral matter (29% in PM10 and 16 % in PM2.5), more than 50% (in PM10) being attributable to African dust. The amount of secondary inorganic aerosols is also very high (27% in PM10 and 34% in PM2.5), with the predominance of fine ammonium sulphate, and in a less proportion fine ammonium nitrate (in winter) and coarse Ca and Na nitrate (with higher importance in summer). The carbonaceous particles, dominantly fine, account for 17% of PM10 and 25% of PM2.5. The elemental carbon/organic carbon (EC/OC) ratio reached a mean value of 0.17, similar to those observed at regional background sites in the WMB coast of Spain. The sea spray aerosols (mainly coarse) represented around 10% of PM10, and only 4% in PM2.5. Finally, the unaccounted fraction increased from 15% to 20% in PM2.5, being mostly attributed to water.The concentrations of trace elements in PM10 and PM2.5 were usually in the range to those observed in regional background sites in the Iberian Peninsula, with the exception of the typical tracers of road traffic such as Cu, Sb, Zn, Sn and Ba, which presented concentrations in the range of urban sites of Iberia. Other elements such as Cr, Zr, Hf and Co have been identified as the main tracers of the harbour contributions.  相似文献   

11.
青海瓦里关大气气溶胶元素富集特征及其来源   总被引：15，自引：3，他引：15       下载免费PDF全文
利用中子活化及PIXE和可见光灰度仪, 对青海瓦里关大气本底基准监测站的大气气溶胶样品进行了测量。通过元素相对浓度、富集因子和主因子分析等数据统计分析, 并结合同期的气团后退轨迹分布资料, 讨论了瓦里关大气气溶胶元素的组成及来源。结果表明, 位于青藏高原偏远地区的瓦里关大气气溶胶以土壤及地壳等自然来源为主, 因子分析的方差百分数给出瓦里关气溶胶中自然源的贡献率平均在70%以上。燃煤、交通及冶炼等人为源也占有一定比例。大气黑碳气溶胶的观测也表明人类活动影响的存在。人为源的影响多与来自东部及河西走廊等经济发达地区的气流有关。  相似文献   

12.
北京秋季气溶胶化学成分的高分辨率观测及来源分析   总被引：2，自引：0，他引：2  
2001年9月30日～10月6日在北京北三环和北四环之间的中国科学院大气物理研究所气象塔院内使用步进采样仪对气溶胶进行了高分辨率连续采样(每2h采集1个样品),并对样品用PIXE方法进行了元素分析,得到20种元素的浓度。分析结果表明,气溶胶各元素浓度随时间的变化趋势基本一致,且日变化特征显著,早晚出现峰值。降雨期间Ti、Si、Fe等元素浓度急剧下降。S、Pb、Cl、Zn等与人类活动相关的气溶胶元素的富集因子很高。因子分析结果表明,北京秋季大气气溶胶主要源于土壤尘、燃煤尘、工业源和汽车尾气排放等。  相似文献   

13.
Trace elements in tropical African savanna biomass burning aerosols   总被引：2，自引：0，他引：2  
As a part of the FOS/DECAFE experiment, aerosol particles emitted during prescribed savanna fires were collected in January 1991 at Lamto (Ivory Coast), either close to the emission or in ambient air. Analytical transmission electron microscopy pointed out the presence of sub-micrometer soots, salt condensates, vegetation relicts and soil derived particles. The samples were also analyzed for their total particulate matter (TPM) content and elemental composition by PIXE or XRF. At the emission, high concentrations of soil derived elements (Fe and Al) pointed out an intense remobilization process during the fires. Biomass burning emissions contributed to more than 90% of the measured concentrations, of P, Cl, S, K, Cu and Zn, which were found primarily in the fine fraction with the exception of P. Near the emission, K was mainly present as KCl, evolving to K2SO4 in the ambient samples. Trace elements emission factors were obtained for the first time for the African savanna burning and their annual emissions were estimated: our median K emission factor (0.78 g/kg of C) is higher than estimates for other ecosystems (0.2–0.58 g/kg of C); Zn emissions (0.008 Tg/year) account for 4 to 11% of the global anthropogenic emissions.  相似文献   

14.
2008年北京奥运会期间大气气溶胶物理特征分析   总被引：5，自引：0，他引：5  
应用MODIS卫星的气溶胶产品资料和地面的光学粒子计数器的资料,对比分析了北京地区2006、2007、2008年7～9月的气溶胶光学厚度、细粒子光学厚度、Angstrom指数、气溶胶粒子数浓度谱及体积谱,发现2008年北京奥运会期间(7月20日～9月20日)的气溶胶光学厚度比2006、2007年同期明显降低,气溶胶细模态光学厚度占总光学厚度的比上升,Angstrom指数上升,气溶胶细粒子数浓度没有明显相对变化,而粗粒子数浓度则减少约50%.利用大气标高,将MODIS反演的气溶胶柱的质量浓度转化为地面气溶胶质量浓度.用粒子计数器得到的体积谱,在假定气溶胶粒子密度的情况下,计算出其质量浓度.将这两种方法得到的气溶胶质量浓度与国家环境保护部公布的空气质量指数换算得到的可吸入颗粒物(PM10)质量浓度进行比较.结果表明:北京奥运期间空气质量总体达到了国家二级空气质量标准;与2006、2007年同期相比,2008年气溶胶PM10质量浓度明显下降,而这主要是由气溶胶粗粒子的减少引起的.  相似文献   

15.
Size segregated sampling of aerosol particles at the coal-fired power station Šoštanj, Slovenia was performed by a newly developed system. In addition, simultaneous sampling of particles was performed at two locations, Velenje and Veliki vrh, chosen on the basis of long term monitoring of SO2 in the influential area of power plant. The signature of the power plant (e.g. characteristic size distributions of some typical trace elements) was identified. For elements, like As, Mo, Cd and Ga, which are typical for coal combustion, the highest concentrations were observed in the size range between 1 and 4 μm. For Se and sometimes for Ga two modes were identified, first between 0.1 and 0.5 μm and second between 1 and 4 μm. Ratios between the average concentrations of selected elements in fine and coarse particles collected at Veliki vrh (the most influenced location) and Velenje (usually not influenced by the thermo power station) were significantly higher than 1 in the case of Mo and Se for coarse and fine size range, while for As the ratio was higher than 1 for the coarse fraction. Consequently, Mo, Se and As were found as the most important tracers for the emissions from the investigated source. On the basis of the ratios between the concentrations of elements measured in particles at low and high SO2 concentrations at Veliki vrh, Cd was shown to be a typical tracer as well. Our results definitely showed that size segregated measurements of particles at the source and in the influenced area give more precise information on the influence of source to the surrounding region. It was found that patterns of size distributions for typical trace elements observed at the source are found also in the influenced area, i.e. Veliki vrh.  相似文献   

16.
近年来华东地区大气气溶胶的时空特征   总被引：4，自引：1，他引：3  
利用2000年2月—2008年12月的AERONET（AErosol RObotic NETwork）地基观测数据对MODIS/TERRA Collection 005气溶胶光学厚度（aerosol optical thickness;AOT）在华东区域的适用性进行了验证,并利用验证后的MODIS气溶胶产品对华东区域气溶胶光学厚度和尺度分布特征进行了分析。结果表明,（1）通过验证比较,MODIS的AOT在华东区域与AERONET站陆基观测到的AOT具有非常好的一致性,满足美国NASA的设计要求。（2）华东区域的气溶胶光学厚度存在明显的时空分布特征。时间上,在春季和夏季达到最大,而在秋季和冬季最小,表现出明显的季节变化规律。空间上,气溶胶光学厚度受地形影响明显。其高值区主要分布在平原地区,而低值区主要在海拔较高的山区。（3）该区域的气溶胶尺度分布也存在显著的变化特征。在冬、春由于沙尘输送的影响,整个华东区域气溶胶粒子的尺度都比较大,主要以自然生成的沙尘粒子为主。而在夏、秋季由于夏季风和降水的影响,气溶胶粒子的尺度都比较小,以工业排放的人为气溶胶粒子为主。  相似文献   

17.
北京地区夏季背景气溶胶的特征   总被引：3，自引：0，他引：3  
本文通过对观测资料的统计分析和比较研究,初步揭示了北京地区夏季背景气溶胶的一些特征,其中包括元素浓度及其变化、富集因子和气溶胶来源等。  相似文献   

18.
The results of an investigation about the vertical distribution patterns of selected trace elements in an urban environment, as reflected by their accumulation in lichen transplants, are reported. Thalli of the lichen Pseudevernia furfuracea were transplanted in 2 sites in the urban area of Thessaloniki (N Greece), subjected to very different traffic loads: 1) Tsimiski, downtown of Thessaloniki, at one of the busiest streets of the city, a street canyon 2) Toumba, far from the city centre, at the edge of the city, at an open street. In each site, thalli were suspended along a vertical transect at 3, 6, 9 and 12 m, and retrieved after one year. The results showed that while at Toumba the elemental composition of lichen samples was essentially influenced by natural occurrence, mainly airborne soil dust, at Tsimiski also anthropogenic input of pollutants determined by vehicle traffic was involved for some elements such as Cd, Cu, Ni, Pb and Zn. The vertical distribution patterns of heavy metals accumulated in lichens showed that in general elevation has no statistically significant influence on the concentration of most metals, but this was not true for Pb, whose concentrations increased with increasing elevation from ground. Residents may thus be more exposed to high concentrations of Pb than pedestrians.  相似文献   

19.
Size-differentiated concentrations of SPM, F, Cl, NO3, SO4, Na, K, Ca, Mg and NH4 in atmospheric aerosols were measured in a suburban area of Agra city during December 1992 to March 1993. Except for NH4, Cl and Na, all components were found to have a bimodal distribution. The fine fraction was dominated by NH4, K, NO3 and SO4, while Na, Ca, Mg, F and Cl contributed to the coarse fraction. Fifty-eight percent of SO4 and 67% of NO3 were found in the fine mode and the coarse mode comprised 42 and 33% of SO4 and NO3, respectively. SO4 was found to have a peak above the submicron range at 1.1 µm which has been attributed to secondary sulphate formation by heterogeneous oxidation of SO2 on alkaline particles of Ca and Mg. The total aerosol was basic in nature and dominated by the soil-derived acid neutralising components (Ca, Mg and Na).  相似文献   

20.
PIXE is a well established and valuable method for quantitative and qualitative aerosol elemental analysis. Using this method, we have developed a technique to simultaneously analyse the trace-element content in precipitation for elements with Z> 12. Freeze-drying and leaching was used as a nonselective preconcentration technique. A special backing foil to take up the sample liquid to be dried was developed for these experiments. By careful adjustment of the experimental parameters, we reached a detection limit lower than 1 ppb for most detected elements. Thus, it will be possible to analyze precipitation at low concentrations of trace elements which are important for air chemistry and environmental studies.Supported by DFG/Bonn under Sonderforschungsbereich 233.  相似文献   

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