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1.
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
2.
The data, measured by a three-wavelength Integrating Nephelometer over Lanzhou City during the winters of 2001/2002 and 2002/2003 respectively, have been analyzed for investigating the scattering properties of atmospheric aerosols and exploring their relationship and the status of air pollution. The aerosol particle volume distribution is inverted with the measured spectral scattering coefficients. The results show that the daily variation of the aerosol scattering coefficients is in a tri-peak shape. The average ratio of backscattering coefficient to total scattering coefficient at 550 nm is 0.158; there exists an excellent correlation between the scattering coefficients and the concentration of PM10. The average ratio of the concentration of PM10 to the scattering coefficients is 0.37g m^-2, which is contingent on the optical parameters of aerosol particles such as the size distribution, etc.; an algorithm is developed for inverting the volume distribution of aerosol particles by using the histogram and Monte-Carlo techniques, and the test results show that the inversion is reasonable. 相似文献
3.
一次秋季冷锋降水过程气溶胶与云粒子分布的飞机观测 总被引：2，自引：1，他引：1
利用机载PMS（Particle Measuring Systems）测量系统,对2008年10月4—5日石家庄地区一次冷锋降水云系的3次气溶胶和云粒子探测资料进行了分析。结果表明,冷锋过境降水前后,气溶胶粒子分布差异较大。降水发生前,气溶胶粒子平均数浓度约为103cm-3,平均直径为0.95μm;气溶胶主要集中于3000m高度以下的对流层低层,云内气溶胶数浓度明显减少。降水发生后,气溶胶粒子平均数浓度约为102cm-3,比降水前约小1个量级,平均直径为1.28μm;气溶胶主要集中于1200m以下的近地面层,其数浓度随高度增加而降低。气溶胶粒子浓度在低层云区内水平变化较小,而在无云区和云下近地层水平起伏较大。云粒子平均浓度比气溶胶小1～2个量级。气溶胶粒子平均谱主要呈双峰型,而云粒子谱主要为单峰型。 相似文献
4.
Scattering Properties of Atmospheric Aerosols over Lanzhou City and Applications Using an Integrating Nephelometer 总被引：2，自引：0，他引：2
The data, measured by a three-wavelength Integrating Nephelometer over Lanzhou City during the winters of 2001/2002 and 2002/2003 respectively, have been analyzed for investigating the scattering properties of atmospheric aerosols and exploring their relationship and the status of air pollution. The aerosol particle volume distribution is inverted with the measured spectral scattering coefficients. The results show that the daily variation of the aerosol scattering coefficients is in a tri-peak shape. The average ratio of backscattering coefficient to total scattering coefficient at 550 nm is 0.158; there exists an excellent correlation between the scattering coefficients and the concentration of PM10. The average ratio of the concentration of PM10 to the scattering coefficients is 0.37 g m-2, which is contingent on the optical parameters of aerosol particles such as the size distribution, etc.; an algorithm is developed for inverting the volume distribution of aerosol particles by using the histogram and Monte-Carlo techniques, and the test results show that the inversion is reasonable. 相似文献
5.
感应电机矢量控制系统的仿真研究 总被引：6，自引：0，他引：6
根据2008年4—7月黄山大气气溶胶观测资料,研究了气溶胶粒子的数浓度、谱分布特征及其与气象因子的关系,探讨了雾天和非雾天气溶胶颗粒物时间和尺度分布特点。分析发现,黄山光明顶春、夏季大气气溶胶数浓度的平均值分别为3.14×103个/cm3和1.80×103个/cm3,其中超细粒子（粒径小于0.1μm的粒子）在春夏季分别约占总粒子数浓度的79%和68%;高数浓度值集中在粒径0.04～0.12μm;积聚模态气溶胶粒子（0.1～1.0μm）在体积浓度分布和表面积分布中占很大比例。结合气象资料比较了雾天与非雾天气溶胶分布的差异,发现细粒子浓度非雾天大于雾天,而气溶胶数浓度与温度呈正相关,与相对湿度成反相关。结果还发现,黄山在春季以西北风和偏南风为主,西北风时气溶胶数浓度较高,在夏季主要以偏南风,特别是西南风为主,但是气溶胶数浓度的高值多发生在偏东风的条件下。 相似文献
6.
利用2009年石家庄地区的4次机载PMS探测资料,对不同天气条件下大气气溶胶的数浓度、平均直径垂直分布和谱分布及一次晴天条件下的水平分布进行分析。结果表明：PCASP 探头探测的0.1-3.0 μm气溶胶粒子最大数浓度的量级为102-104 cm-3之间,平均值量级为102-103 cm-3之间,平均直径最大值介于0.225-0.717 μm,平均值介于0.148-0.167 μm。晴天条件下,气溶胶的数浓度随高度递减,直径随高度变化不大;逆温层底气溶胶明显积累,气溶胶浓度在大气边界层内明显高于其他层次;阴天轻雾情况下边界层内的气溶胶数浓度大于雨天和晴天,雨天气溶胶浓度最低;晴天气溶胶数浓度的水平分布不均匀;在云中气溶胶浓度明显下降,在云外气溶胶浓度较高。不同天气条件和晴天不同高度情况下,石家庄地区气溶胶谱型呈单峰分布,小于0.3 μm的细粒子对气溶胶的数浓度贡献最大,且随着高度的增加谱宽变窄。 相似文献
7.
As a component of the Canadian Arctic Haze Study, held coincident with the second Arctic Gas and Aerosol Sampling Program (AGASP II), vertical profiles of aerosol size distribution (0.17 m), light scattering parameters and cloud particle concentrations were obtained with an instrumented aircraft and ground-based lidar system during April 1986 at Alert. Northwest Territories. Average aerosol number concentrations range from about 200 cm–3 over the Arctic ice cap to about 100 cm–3 at 6 km. The aerosol size spectrum is virtually free of giant or coarse aerosol particles, and does not vary significantly with altitude. Most of the aerosol volume is concentrated in the 0.17–0.50 m size range, and the aerosol number concentration is found to be a good surrogate for the SO4
= concentration of the Arctic haze aerosol. Comparison of the aircraft and lidar data show that, when iced crystal scattering is excluded, the aerosol light scattering coefficient and the lidar backscattering coefficient are proportional to the Arctic haze aerosol concentration. Ratios of scattering to backscattering, scattering to aerosol number concentration, and backscattering to aerosol number concentration are 15.3 steradians, 1.1×10–13 m2, and 4.8×10–15 m2 sr–1, respectively. Aerosol scattering coefficients calculated from the measured size distributions using Mie scattering agree well with measured values. The calculations indicate the aerosol absorption optical depth over 6 km to range between 0.011 and 0.018. The presence of small numbers of ice crystals (10–20 crystals 1–1 measured) increased light scattering by over a factor of ten. 相似文献
8.
沙尘传输路径上气溶胶浓度与干沉降通量的粒径分布特征 总被引：1，自引：0，他引：1
利用2002年春季中国北京、青岛和日本福冈3个地区的分级气溶胶浓度资料,结合改进的Wil-liams模型,分析了沙尘传输路径上空气动力学直径≤11μm气溶胶(PM11)浓度和干沉降通量的粒径分布特征,并估算了黄海海域春季PM11的干沉降通量及不同粒径气溶胶的贡献。结果表明:3个地区PM11浓度粒径分布在非沙尘时期呈双峰分布,两个峰值分别出现在细颗粒(<2.1μm)部分和粗颗粒(2.1～11μm)部分;沙尘时期,3个地区PM11浓度粒径分布均趋于单峰分布,峰值位于粗颗粒部分,并且越靠近沙尘源地,这种趋势越明显。较强沙尘天气时期,粗颗粒部分的浓度峰值粒径从沙尘源地附近到黄海西岸、东岸呈降低趋势,但在一般沙尘天气时期,这种现象并不明显。沙尘时期和非沙尘时期,3个地区粗颗粒的干沉降通量均随粒径增加而增大,细颗粒的干沉降通量随粒径的变化不明显。虽然沙尘时期粗颗粒沉降通量较非沙尘时期有明显增加,但粗颗粒对PM11干沉降通量的贡献与非沙尘时期相比,并没有明显的变化。较强沙尘天气时期,3个地区粗颗粒的干沉降通量明显高于一般沙尘天气时期;细颗粒的干沉降通量较一般沙尘天气时期略有增加。黄海海域春季沙尘时期PM11的干沉降通量约为31.70～58.59mg.m-2.d-1,非沙尘时期约为8.33～15.94mg.m-2.d-1。粗颗粒是黄海海域春季PM11干沉降通量的主要贡献者,约占PM11干沉降通量的94.2%以上。 相似文献
9.
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
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.
Frank Drewnick Johannes Schneider Silke S. Hings Nele Hock Kevin Noone Admir Targino Silke Weimer Stephan Borrmann 《Journal of Atmospheric Chemistry》2007,56(1):1-20
The Aerodyne aerosol mass spectrometer (Q-AMS) was coupled with a counterflow virtual impactor (CVI) for the first time to measure cloud droplet residuals of warm tropospheric clouds on Mt. Åreskutan in central Sweden in July 2003. Operating the CVI in different operational modes generated mass concentration and species-resolved mass distribution data for non-refractory species of the ambient, interstitial, and residual aerosol. The ambient aerosol measurements revealed that the aerosol at the site was mainly influenced by long-range transport and regional photochemical generation of nitrate and organic aerosol components. Four different major air masses were identified for the time interval of the experiment. While two air masses that approached the site from northeastern Europe via Finland showed very similar aerosol composition, the other two air masses from polar regions and the British Islands had a significantly different composition. During cloud events the larger aerosol particles were found to be activated into cloud droplets. On a mass basis the activation cut-off diameter was approximately 150 nm for nitrate and organics dominated particles and 200 nm for sulfate dominated particles. Generally nitrate and organics were found to be activated into cloud droplets with higher efficiency than sulfate. While a significant fraction of the nitrate in ambient particles was organic nitrates or nitrogen-containing organic species, the nitrate found in the cloud droplet residuals was mainly ammonium nitrate. After passage of clouds the ambient aerosol size distribution had shifted to smaller particle sizes due to the predominantly activation of larger aerosol particles without a significant change in the relative composition of the ambient aerosol. 相似文献
12.
利用2014年7月黄山光明顶观测获得的气溶胶数浓度、气溶胶数谱数据,对黄山夏季气溶胶数浓度及谱分布特征进行分析,并在此基础上对气溶胶数谱进行了对数正态分布拟合。研究结果表明:黄山夏季气溶胶平均数浓度约为3 518.27 cm~(-3),主要集中在爱根核模态;气溶胶平均数浓度日变化呈双峰分布,峰值浓度的出现伴随着小粒子的增多。气溶胶数浓度与相对湿度和风速成负相关,高浓度的气溶胶多出现在较弱的东南风时;积聚模态气溶胶数浓度受风向影响显著。不同气团背景下气溶胶数谱差异集中在小于100 nm和500~1 000 nm粒径范围。爱根核模态气溶胶在高湿的西南气团影响下数浓度最低、谱较窄,而高温、低湿的东南气团对应的气溶胶数浓度最高、谱最宽,北方气团对应的气溶胶数浓度和谱宽居中;500~1 000 nm粒径范围气溶胶数谱分布特征与之相反。不同背景的气溶胶数谱和体积谱均可采用爱根模态、积聚模态1和积聚模态2三个模态进行对数正态分布拟合,但不同气团背景下的各模态谱型参数差异较大。 相似文献
13.
Randolph D. Borys Edward E. Hindman Paul J. DeMott 《Journal of Atmospheric Chemistry》1988,7(3):213-239
The relationships between the physical and chemical properties of mixed-phase clouds were investigated at Storm Peak Laboratory (3220m MSL) located near the continental divide in northwestern Colorado. Interstitial aerosol particles, cloud droplets and snow crystals were concurrently collected when the laboratory was enveloped by a precipitating cloud. All samples were analyzed for trace elements, soluble anions, electrical conductivity and acidity.The results show average trace constituent concentration ratios of cloud water to snow water range from 0.4 to 26. All but six of the 32 elements and ions measured had ratios greater than one. This result suggests a chemical species dependency of in-cloud aerosol particle scavenging processes. Evidence of a decrease of in-cloud aerosol particle scavenging efficiency by snow due to increases in aerosol concentration is also presented.Differences between the chemical composition of cloud water and snow water are manifested most strongly when snow crystals grow by vapor deposition. In-cloud scavenging efficiencies by snow crystals for most aerosol particle chemical species are dependent on the growth of the snow crystals by accretion of cloud droplets. This chemical fractionation of the atmospheric aerosol by snow crystal formation and growth should be most active where narrow, continental cloud droplet size distributions and low liquid water contents are prevalent, enhancing the probability of snow crystal growth by diffusion. 相似文献
14.
分别利用碳成分分析仪、离子色谱仪和原子吸收光谱仪等获取浙江省临安地区大气气溶胶在春、夏、秋、冬四季的质量浓度、离子与碳成分特性，并对不同粒径气溶胶成分分布特点作了较详细分析。结果表明:气溶胶质量浓度、可溶性离子浓度以及碳成分浓度具有明显的季节变化趋势。整个尺度范围内，气溶胶质量浓度季节变化特点为春季浓度最高，达到534 μg/m3；冬季次之，质量浓度为117.21 μg/m3；夏季浓度最低，平均为65.7 μg/m3；秋季质量浓度98.6 μg/m3。可溶性离子成分在气溶胶中所占比例具有明显的季节性，其中夏季最高为49.4%，春季最低为11.3%。硫酸根离子SO42-和氨根离子NH4+和硝酸根离子NO3- 3种离子浓度之和约占离子总量的75%~83%。受温度影响，硝酸根离子NO3-浓度随季节变化幅度较大，夏季平均浓度为1.7 μg/m3, 冬季平均浓度为11.5 μg/m3，是夏季浓度的6.8倍。碳浓度分布特点显示，气溶胶中元素碳浓度春季最高，夏季最低。有机碳浓度春季最高，冬季最低。气溶胶粒度分布特点也非常明显。四季中粒径小于11 μm（PM11）的气溶胶均占气溶胶总量的90%以上，粒径小于2.1 μm（PM2.1）的气溶胶占到气溶胶总量的53%以上。可溶性离子在粒径小于2.1 μm气溶胶颗粒中，以硫酸根离子、氨根离子和硝酸根离子为主。碳成分尺度分布特征为颗粒越小，有机碳及元素碳浓度越高。 相似文献
15.
The change of the chemical composition of the near-ground level atmospheric aerosol was studied during two summer episodes by a Lagrangian type of experimental approach. Bulk and single-particle chemical analyses of ions and elements in the particulate phase were deployed. N(-III) and N(V) components were also measured in the gas-phase. The measurements were completed by particle size distributions.Secondary inorganic aerosols (SIA) and fine particles of ≈0.2–0.4 μm size were still elevated 50 km downwind of the city. The direct comparison of transport over the city in contrast to transport over the surrounding areas showed that SIA was formed from emission from the city within less than 3 h. Relative increases, i.e., enrichment during transport were observed for primary and secondary aerosol components. The degree of mixing on the individual particle level increased significantly during transport in the area. In particular, newly emitted carbonaceous particles became internally mixed within hours with pre-existing sulphate particles. Mostly due to secondary aerosol formation the average particle size (mass median diameter) of major constituents of the aerosol was significantly decreased while being transported over 13 h. Given recent insights which link fine particles number and mass concentrations with health risks, the results suggest that rural populations in areas which frequently are located within an urban plume might run an elevated health risk relative to populations in areas not affected by urban plumes. 相似文献
16.
利用2014年7月在黄山光明顶观测的气溶胶吸湿性参数（κ）和气溶胶离子化学组分、有机碳（OC,organic carbon）数据,对多尺度气溶胶吸湿性参数进行分析,并在此基础上建立了多尺度κ的参数化方案。研究结果表明,影响黄山夏季气溶胶来源的主要气团包括西南气团、北方气团以及东南气团。黄山夏季κ的变化范围为0.2-0.48,且随粒径增大成先增大后减小的分布特征;气溶胶粒径在0.15-1.1 μm的强吸湿段,κ>0.3,而在粒径小于0.15 μm和粒径大于1.1 μm弱吸湿段,κκ分布不同,气溶胶粒子在小于1.1 μm的粒径段,当受西南气团影响时,κ值最大,而受东南气团影响时,κ值最小;在气溶胶粒径大于1.1 μm时,κ在两个气团背景下呈现与气溶胶粒径小于1.1 μm时相反的分布特征。影响粒径小于1.1 μm气溶胶吸湿能力的主要水溶性化学组分为NH4+、SO42-、水溶性有机碳（WSOC,water soluble organic carbon）,而影响大于1.1 μm粒径范围气溶胶吸湿能力的主要水溶性化学组分为NH4+、SO42-、NO3-、WSOC和Ca2+。由气溶胶多尺度离子化学组分和WSOC构建的气溶胶κ的参数化方案,在小于1.1 μm和大于1.1 μm的粒径范围内的表达式分别为κreg=0.12+0.45fNH4++0.63fSO42-+0.18fWSOC和κreg=0.01+0.78fNH4++0.76fNO3-+0.8fSO42--0.28fCa2++0.14fWSOC（f为对应组分的质量份数）。两个参数化方案均能较好地预报κ,预报值κreg与κ的计算值间存在较好的相关关系,相关系数通过了置信度99%的显著性检验,且预报误差在30%范围内。 相似文献
17.
Nucleation scavenging and the formation of a cloud interstitial aerosol (CIA) were theoretically studied in terms of the chemical composition of atmospheric aerosol particles. For this study, we used our air-parcel cloud model, which includes the entrainment of air and detailed microphysics, for determining the growth and interaction of aerosol particles and drops. Maritime and remote continental aerosol particle spectrums were used whose size distributions were superpositions of three log-normal distributions, each of a prescribed chemical composition. Our results show (1) that the CIA exhibits a size distribution with a distinctive cut-off at a specific radius of the dry as well as of the wet particle size distribution. All particles above this limiting size become activated to cloud drops and, thus, are not present in the CIA spectrum. This limiting size was found to be independent of the chemical composition of the particles and only dependent on the prevailing supersaturation. Below this specific size, the CIA spectrum becomes depleted of dry aerosol particles in a manner which does depend on their chemical composition and on the supersaturation in the air. (2) The number of aerosol particles nucleated to cloud drops depends critically on the chemical composition of the particles and on the prevailing supersaturation. 相似文献
18.
Hygroscopic growth of aerosol particles and its influence on nucleation scavenging in cloud: Experimental results from Kleiner Feldberg 总被引：8，自引：0，他引：8
Birgitta Svenningsson Hans-Christen Hansson Alfred Wiedensohler Kevin Noone John Ogren Anneli Hallberg Roy Colvile 《Journal of Atmospheric Chemistry》1994,19(1-2):129-152
The hygroscopic growth of individual aerosol particles has been measured with a Tandem Differential Mobility Analyser. The hygroscopic growth spectra were analysed in terms of diameter change with increasing RH from 20% to 85%. The measurements were carried out during the GCE cloud experiment at Kleiner Feldberg, Taunus, Germany in October and November 1990.Two groups of particles with different hygroscopic growth were observed. The less-hygroscopic group had average growth factors of 1.11, 1.04 and 1.02 for particle diameters of 50, 150 and 300 nm, respectively. The more-hygroscopic group had average growth factors of 1.34, 1.34, and 1.37 for the same particle diameters. The average fraction of less-hygroscopic particles was about 50%. Estimates of the soluble fractions of the particles belonging to the two groups are reported.Hygroscopic growth spectra for total aerosol, interstitial aerosol and cloud drop residuals were measured. A comparison of these hygroscopic growths of individual aerosol particles provides clear evidence for the importance of hygroscopic growth in nucleation scavenging. The measured scavenged fraction of particles as a function of diameter can be explained by the hygroscopic growth spectra. 相似文献
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天空辐射计观测2006年春季北京地区气溶胶光学特性的研究 总被引：2，自引：0，他引：2
利用2006年3～5月天空辐射计观测数据反演得到北京地区春季大气气溶胶光学性质参数,包括大气气溶胶光学厚度(0.5μm)、Angstrm指数、单次散射反射比和粒子谱分布特征。结果表明:北京地区春季气溶胶平均光学厚度0.67,Angstrm指数0.54,单次散射比0.88,粒子吸收性质较弱,粒子谱呈双峰形,以粗粒子为主,粗、细模态粒子粒径分别集中在0.17μm和7.7μm左右。相比2004年此次观测期间气溶胶粒径较大,粒子体积浓度较高,散射作用在其消光特性中的比重略有下降。光学厚度日变化呈单峰型,日间单次散射比随时间逐渐递减,Angstrm指数在上午递减趋势明显,午后变得稳定。对同时观测的天空辐射计与CE-318不同波长光学厚度结果进行比较,结果显示两者得到的光学厚度相关性很好,各波长小时平均结果的相对误差小于7%。 相似文献