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1.
Urban aerosols have a large effect on the deterioration of air quality and the degradation of atmospheric visibility.Characterization of the chemical composition of PM 2.5 and in situ measurements of the optical properties of aerosols were conducted in July 2008 at an urban site in Guangzhou,Southern China.The mean PM 2.5 concentration for the entire period was 53.7±23.2 μg m 3.The mean PM 2.5 concentration (82.7±25.4 μg m 3) on hazy days was roughly two times higher than that on clear days (38.8±8.7 μg m 3).The total water-soluble ion species and the total average carbon accounted for 47.9%±4.3% and 35.2%±4.5%,respectively,of the major components of PM 2.5.The increase of secondary and carbonaceous aerosols,in particular ammonium sulfate,played an important role in the formation of haze pollution.The mean absorption and scattering coefficients and the single scattering albedo over the whole period were 53±20 M m 1,226±111 M m 1,and 0.80±0.04,respectively.PM 2.5 had a high linear correlation with the aerosol extinction coefficient,elemental carbon (EC) was correlated with aerosol absorption,and organic carbon (OC) and SO 4 2 were tightly linked to aerosol scattering.  相似文献   

2.
The hygroscopic properties of mixed aerosol particles are crucial for the application of remote sensing products of aerosol optical parameters in the study of air quality and climate at multiple scales. In this study, the authors investigated aerosol optical properties as a function of relative humidity (RH) for two representative metropolises: Beijing and Hong Kong. In addition to the RH data, mass concentrations of PM 10 (particulate matter up to 10 μm in diameter) and aerosol scattering extinction coefficient (σ ext ) data were used. The relationship between the mass scattering extinction efficiency (MEE, defined as σ ext /PM 10 ) and RH can be expressed by regression functions as f = 1.52x + 0.29 (r2 = 0.77), f = 1.42x + 1.53 (r2 = 0.58), f = 1.19x + 0.65 (r2 = 0.59), and f = 1.58x + 1.30 (r2 = 0.61) for spring, summer, autumn, and winter, respectively, in Beijing. Here, f represents MEE, x represents 1/(1 RH), and the coefficients of determination are pre- sented in parentheses. Conversely, in Hong Kong, the corresponding functions are f = 1.98x 1.40 (r2 = 0.55), f = 1.32x 0.36 (r2 = 0.26), f = 1.87x 0.65 (r2 = 0.64), and f = 2.39x 1.47 (r2 = 0.72), respectively. The MEE values for Hong Kong at high RHs (RH 70%) are higher than those for Beijing, except in summer; this suggests that aerosols in Hong Kong are more hygroscopic than those in Beijing for the other three seasons, but the aerosol hygroscopicity is similarly high in summer over both cities. This study describes the effects of moisture on aerosol scattering extinction coefficients and provides a potential method of studying atmospheric visibility and groundlevel air quality using some of the optical remote sensing products of satellites.  相似文献   

3.
Few studies have specifically focused on the validation and spatiotemporal distribution of planetary boundary layer height(PBLH) and relative humidity(RH) data in China. In this analysis, continuous PBLH and surface-level RH data simulated from GEOS-5 between 2004 and 2012, were validated against ground-based observations. Overall, the simulated RH was consistent with the statistical data from meteorological stations, with a correlation coefficient of 0.78 and a slope of 0.9. However, the simulated PBLH was underestimated compared to LIDAR data by a factor of approximately two,which was primarily because of poor simulation in late summer and early autumn. We further examined the spatiotemporal distribution characteristics of two factors in four regions—North China, South China, Northwest China, and the Tibetan Plateau. The results showed that the annual PBLH trends in all regions were fairly moderate but sensitive to solar radiation and precipitation, which explains why the PBLH values were ranked in order from largest to smallest as follows: Tibetan Plateau, Northwest China, North China, and South China. Strong seasonal variation of the PBLH exhibited high values in summer and low values in winter, which was also consistent with the turbulent vertical exchange. Not surprisingly, the highest RH in South China and the lowest RH in desert areas of Northwest China(less than 30%). Seasonally, South China exhibited little variation, whereas Northwest China exhibited its highest humidity in winter and lowest humidity in spring,the maximum values in the other regions were obtained from July to September.  相似文献   

4.
 A statistic regression approach was used to estimate the wavelength exponents of black carbon (BC) and dust particles, and further to separate the contributions of the two types of aerosols to the total light absorption coefficient measured in the Beijing urban area in the spring of 2006. The results show that the wavelength exponent (a) of black carbon aerosol at urban site was approximately -0.92, which is in agreement with the value of -0.8±0.2 reported in related studies. The decoupling analysis of the measured light absorption coefficients during the three floating dust periods ( March 25, March 27, and April 9) demonstrates that, on average, the light absorption caused by dust particles took up about 32.8% of the total light absorption at 520 nm wavelength, and by black aerosol more than 60%. This indicates that the black carbon was still the major contributor to the total aerosol light absorption in Beijing urban area even during the floating dust periods.  相似文献   

5.
To investigate aerosol optical properties in the Beijing metropolitan area,aerosol absorption coefficient(Ab) ,scattering coefficient(Sc) ,and fine particulate matter(PM2.5) were measured in the Beijing urban area from 20 May to 30 August 2009.The average Ab,Sc,single scattering albedo(SSA) ,and PM2.5 concentration were 58.0±39.5 M m-1,343.5±353.7 M m-1,0.80±0.10 and 63.6±50.0-g m-3,respectively,during the observation period.Ab,Sc,and SSA all showed single peak diurnal variations,with their maximum values being measured at 0500,1000,and 1300 local time,respectively.Ab and Sc had a strong positive correlation with PM2.5,and Ab,Sc,and PM2.5 all had positive correlations with relative humidity and negative correlations with wind speed.  相似文献   

6.
This paper explores the role of the secondary inorganic aerosol (SIA) species ammonium,NH4+,nitrate,NO3-,and sulfate,SO24-,during haze and fog events using hourly mass concentrations of PM2.5 measured at a suburban site in Hangzhou,China.A total of 546 samples were collected between 1 April and 8 May 2012.The samples were analyzed and classified as clear,haze or fog depending on visibility and relative humidity (RH).The contribution of SIA species to PM2.5 mass increased to ~50% during haze and fog.The mass contribution of nitrate to PM2.5 increased from 11% during clear to 20% during haze episodes.Nitrate mass exceeded sulfate mass during haze,while near equal concentrations were observed during fog episodes.The role of RH on the correlation between concentrations of SIA and visibility was examined,with optimal correlation at 60%-70% RH.The total acidity during clear,haze and fog periods was 42.38,48.38 and 45.51 nmol m-3,respectively,indicating that sulfate,nitrate and chloride were not neutralized by ammonium during any period.The nitrate to sulfate molar ratio,as a function of the ammonium to sulfate molar ratio,indicated that nitrate formation during fog started at a higher ammonium to sulfate molar ratio compared to clear and haze periods.During haze and fog,the nitrate oxidation ratio increased by a factor of 1.6-1.7,while the sulfur oxidation ratio increased by a factor of 1.2-1.5,indicating that both gaseous NO2 and SO2 were involved in the reduced visibility.  相似文献   

7.
The profiles of aerosol extinction coefficients are investigated by micro-pulse lidar(MPL)combined with the meteorological data in the lower troposphere at Meteorological ResearchInstitute(MRI).Japan.Larger extinction values of aerosol are demonstrated in the nocturnalstable air layer with larger Richardson number,and light wind velocities are favorable for aerosolconcentrating in the planetary boundary layer(PBL).But aerosol extinction coefficients showlarger values over the altitudes of 2.0 to 5.0km where correspond to higher relative humidity(RH).The tops of PBL identified by the aerosol extinction profiles almost agree with ones byradiosonde data.The diurnal variations of aerosol extinction profiles are clearly displayed,intensive aerosol layers usually are formed over the period of mid-morning to 1400 Loeal Time(LT).then elapse in the cloudless late afternoon and nighttime.Thermal eonvection or turbulenttransport from the surfaee probably dominates these temporal and spatial changes of aerosoldistribution.  相似文献   

8.
Wavelet analysis was applied to lidar observations to retrieve the planetary boundary layer height(PBLH)over Guangzhou from September 2013 to November 2014 over Guangzhou. Impact of the boundary effect and the wavelet scale factor on the accuracy of the retrieved PBLH has been explored thoroughly. In addition, the PBLH diurnal variations and the relationship between PM_(2.5) concentration and PBLH during polluted and clean episodes were studied. Results indicate that the most steady retrieved PBLH can be obtained when scale factor is chosen between 300-390 m. The retrieved maximum and minimum PBLH in the annual mean diurnal cycle were ~1100 m and ~650 m, respectively. The PBLH was significantly lower in the dry season than in the wet season, with the average highest PBLH in the dry season and the wet season being ~1050 m and ~1200 m respectively. Compared to the wet season, the development of PBLH in the dry season was delayed by at least one hour due to the seasonal cycle of solar radiation. Episode analysis indicated that the PBLH was ~50% higher during clean episodes than during haze episodes. The average highest PBLH in the haze episodes and clean episodes were ~800 m and ~1300 m,respectively. A significant negative correlation between PBLH and PM_(2.5) concentration(r =-0.55**) is discovered.According to China"Ambient Air Quality Standard", the PBLH values in good and slightly polluted conditions were 1/6-1/3 lower than that in excellent conditions, while the corresponding PM_(2.5) concentration were ~2-2.5 times higher.  相似文献   

9.
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   

10.
The marine atmospheric boundary layer (MABL) plays a vital role in the transport of momentum and heat from the surface of the ocean into the atmosphere. A detailed study on the MABL characteristics was carried out using high-resolution surface-wind data as measured by the QuikSCAT (Quick scatterometer) satellite. Spatial variations in the surface wind, frictional velocity, roughness parameter and drag coefficient for the different seasons were studied. The surface wind was strong during the southwest monsoon season due to the modulation induced by the Low Level Jetstream. The drag coefficient was larger during this season, due to the strong winds and was lower during the winter months. The spatial variations in the frictional velocity over the seas was small during the post-monsoon season (~0.2 m s-1). The maximum spatial variation in the frictional velocity was found over the south Arabian Sea (0.3 to 0.5 m s-1) during the southwest monsoon period, followed by the pre-monsoon over the Bay of Bengal (0.1 to 0.25 m s-1). The mean wind-stress curl during the winter was positive over the equatorial region, with a maximum value of 1.5×10-7N m-3, but on either side of the equatorial belt, a negative wind-stress curl dominated. The area average of the frictional velocity and drag coefficient over the Arabian Sea and Bay of Bengal were also studied. The values of frictional velocity shows a variability that is similar to the intraseasonal oscillation (ISO) and this was confirmed via wavelet analysis. In the case of the drag coefficient, the prominent oscillations were ISO and quasi-biweekly mode (QBM). The interrelationship between the drag coefficient and the frictional velocity with wind speed in both the Arabian Sea and the Bay of Bengal was also studied.  相似文献   

11.
Haze-fog conditions over northern India are associated with visibility degradation and severe attenuation of solar radiation by airborne particles with various chemical compositions. PM2.5 samples have been collected in Delhi, India from December 2011 to November 2012 and analyzed for carbonaceous and inorganic species. PM10 measurements were made simultaneously such that PM10–2.5 could be estimated by difference. This study analyzes the temporal variation of PM2.5 and carbonaceous particles (CP), focusing on identification of the primary and secondary aerosol emissions, estimations of light extinction coefficient (bext) and the contributions by the major PM2.5 chemical components. The annual mean concentrations of PM2.5, organic carbon (OC), elemental carbon (EC) and PM10–2.5 were found to be 153.6 ± 59.8, 33.5 ± 15.9, 6.9 ± 3.9 and 91.1 ± 99.9 μg m?3, respectively. Total CP, secondary organic aerosols and major anions (e.g., SO4 2? and NO3 ?) maximize during the post-monsoon and winter due to fossil fuel combustion and biomass burning. PM10–2.5 is more abundant during the pre-monsoon and post-monsoon. The OC/EC varies from 2.45 to 9.26 (mean of 5.18 ± 1.47), indicating the influence of multiple combustion sources. The bext exhibits highest values (910 ± 280 and 1221 ± 371 Mm?1) in post-monsoon and winter and lowest in monsoon (363 ± 110 and 457 ± 133 Mm?1) as estimated via the original and revised IMPROVE algorithms, respectively. Organic matter (OM =1.6 × OC) accounts for ~39 % and ~48 % of the bext, followed by (NH4)2SO4 (~21 % and ~24 %) and EC (~13 % and ~10 %), according to the original and revised algorithms, respectively. The bext estimates via the two IMPROVE versions are highly correlated (R2 = 0.95, root mean square error = 38 % and mean bias error = 28 %) and are strongly related to visibility impairment (r = ?0.72), mostly associated with anthropogenic rather than natural PM contributions. Therefore, reduction of CP and precursor gas emissions represents an urgent opportunity for air quality improvement across Delhi.  相似文献   

12.
The new European Council Directive (PE-CONS 3696/07) frames the inhalable (PM10) and fine particles (PM2.5) on priority to chemically characterize these fractions in order to understand their possible relation with health effects. Considering this, PM2.5 was collected during four different seasons to evaluate the relative abundance of bulk elements (Cl, S, Si, Al, Br, Cu, Fe, Ti, Ca, K, Pb, Zn, Ni, Mn, Cr and V) and water soluble ions (F, Cl, NO2 , NO3 , SO4 2−, Na+, NH4 +, Ca2+ and Mg2+) over Menen, a Belgian city near the French border. The air quality over Menen is influenced by industrialized regions on both sides of the border. The most abundant ionic species were NO3 , SO4 2− and NH4 +, and they showed distinct seasonal variation. The elevated levels of NO3 during spring and summer were found to be related to the larger availability of the NOx precursor. The various elemental species analyzed were distinguished into crustal and anthropogenic source categories. The dominating elements were S and Cl in the PM2.5 particles. The anthropogenic fraction (e.g. Zn, Pb, and Cu) shows a more scattered abundance. Furthermore, the ions and elemental data were also processed using principal component analysis and cluster analysis to identify their sources and chemistry. These approach identifies anthropogenic (traffic and industrial) emissions as a major source for fine particles. The variations in the natural/anthropogenic fractions of PM2.5 were also found to be a function of meteorological conditions as well as of long-range transport of air masses from the industrialized regions of the continent. Electronic supplementary material  The online version of this article (doi:) contains supplementary material, which is available to authorized users.  相似文献   

13.
Long-term measurements of ambient particulate matter less than 2.5 μm in diameter (PM2.5) and its chemical compositions were performed at a rural site in Korea from December 2005 to August 2009. The average PM2.5 concentration was 31 μg m−3 for the whole sampling period, and showed a slightly downward annual trend. The major components of PM2.5 were organic carbon, SO42−, NO3, and NH4+, which accounted for 55 % of total PM2.5 mass on average. For the top 10 % of PM2.5 samples, anionic constituents and trace elements clearly increased while carbonaceous constituents and NH4+ remained relatively constant. Both Asian dust and fog events clearly increased PM2.5 concentrations, but affected its chemical composition differently. While trace elements significantly increased during Asian dust events, NO3, NH4+ and Cl were dramatically enhanced during fog events due to the formation of saturated or supersaturated salt solution. The back-trajectory based model, PSCF (Potential Source Contribution Function) identified the major industrial areas in Eastern China as the possible source areas for the high PM2.5 concentrations at the sampling site. Using factor analysis, soil, combustion processes, non-metal manufacture, and secondary PM2.5 sources accounted for 77 % of the total explained variance.  相似文献   

14.
Severe air pollution with visibility deterioration has long been a focus in the North China Plain (NCP). In this study, concentration and light extinction analysis of PM2.5 chemical components were carried out from 2014 to 2017 to study the pollution characteristics in Baoding, a case city of the NCP. The annual average concentration of total PM2.5 components showed a declining trend, decreasing by 11 µg m−3 (water-soluble inorganic ions), 23 µg m−3 (carbonaceous aerosols), and 1796 ng m−3 (inorganic elements). Contributing 82.9% to the concentration of total ions, the dominant components, NH4+, NO3, and SO42− became the main pollutants in PM2.5 pollution. Based on the IMPROVE algorithm, the average reconstructed PM2.5 mass concentration was 93 ± 69 µg m−3 during the observation period. Meanwhile, the light extinction coefficients were 373.8 ± 233.6 M m−1, 405.3 ± 300.1 M m−1, 554.3 ± 378.2 M m−1 and 1005.2 ± 750.3 M m−1, in spring, summer, autumn, and winter, respectively. Ammonium sulfate, ammonium nitrate, and organic matter were the largest contributors to light extinction, accounting for a total of 55%–77% in the four seasons. The bsca (light scattering by particles and gases) reconstructed from PM2.5 components (Rbsca) and the bsca converted from visibility (Vbsca) were compared to evaluate the performance of the IMPROVE algorithm, revealing a high correlation coefficient of 0.84. The high values of Vbsca were underestimated while the low values were overestimated, as determined through comparison with the one-to-ne line. Especially, when Rbsca > 1123 M m−1 (corresponding to < 2.0 km, approximately), Vbsca was underestimated by 17.6%. PM2.5 mass concentration and relative humidity also had an impact on the estimation.摘要华北平原大气污染与低能见度状况一直是人们关切的问题.本文通过分析2014 - 2017年PM2.5化学成分的浓度和消光效果, 研究了华北平原典型城市保定市的大气污染特征.结果表明, PM2.5组分的年均浓度显示下降趋势, 水溶性无机离子,碳质气溶胶和金属元素分别减少了11 µg m−3, 23 µg m−3和1796 ng m−3.NH4+,NO3和SO42−是PM2.5污染的主要污染物, 三者之和占总离子浓度的82.9%.基于IMPROVE方程对细颗粒物进行重构, 在观测期间PM2.5质量浓度平均为93 ± 69 µg m−3, 春季,夏季,秋季和冬季的消光系数分别为373.8 ± 233.6 M m−1,405.3 ± 300.1 M m−1,554.3 ± 378.2 M m−1和1005.2 ± 750.3 M m−1.硫酸铵,硝酸铵和有机物对消光的贡献最大, 不同季节下占比达55% ~77%.通过PM2.5组分进行重构, 利用IMPROVE算法计算得到Rbsca, 用能见度测量值转换得到Vbsca, 二者具有较高的相关性 (r2=0.84) ;但存在Vbsca的高值被低估, Vbsca的低值被高估的现象;特别是当Rbsca > 1123 M m−1 (对应能见度约小于2.0 km) 时, Vbsca的值被低估了17.6%.高浓度PM2.5和高湿度对IMPROVE算法结果有显著的影响.  相似文献   

15.
Beijing is one of the largest and most densely populated cities in China. PM2.5 (fine particulates with aerodynamic diameters less than 2.5 μm) pollution has been a serious problem in Beijing in recent years. To study the temporal and spatial variations in the chemical components of PM2.5 and to discuss the formation mechanisms of secondary particles, SO2, NO2, PM2.5, and chemical components of PM2.5 were measured at four sites in Beijing, Dingling (DL), Chegongzhuang (CG), Fangshan (FS), and Yufa (YF), over four seasons from 2012 to 2013. Fifteen chemical components, including organic carbon (OC), elemental carbon (EC), K+, NH4 +, NO3 ?, SO4 2?, Cl?, Al, Ca, Fe, Mg, Na, Pb, Si, and Zn, were selected for analysis. Overall, OC, SO4 2?, NO3 ?, and NH4 + were dominant among 15 components, the annual average concentrations of which were 22.62 ± 21.86, 19.39 ± 21.06, 18.89 ± 19.82, and 13.20 ± 12.80 μg·m?3, respectively. Compared with previous studies, the concentrations of NH4 + were significantly higher in this study. In winter, the average concentrations of OC and EC were, respectively, 3 and 2.5 times higher than in summer, a result of coal combustion during winter. The average OC/EC ratios over the four sites were 4.9, 7.0, 8.1, and 8.4 in spring, summer, autumn, and winter, respectively. The annual average [NO3 ?]/[SO4 2?] ratios in DL, CG, FS, and YF were 1.01, 1.25, 1.08, and 1.12, respectively, which were significantly higher than previous studies in Beijing, indicating that the contribution ratio of mobile source increased in recent years in Beijing. Analysis of correlations between temperature and relative humidity and between SOR ([SO4 2?]/([SO4 2?] + [SO2])) and NOR ([NO3 ?]/([NO3 ?] + [NO2])) indicated that gas-phase oxidation reactions were the major formation mechanism of SO4 2? in spring and summer in urban Beijing, whereas slow gas-phase oxidation reactions and heterogeneous reactions both occurred in autumn and winter. NO3 ? was mainly formed through year-round heterogeneous reactions in urban Beijing.  相似文献   

16.
Aerosol size distributions were measured with Micro Orifice Uniform Deposit Impactor (MOUDI) cascade impactors at the rural Angiola and urban Fresno Supersites in California's San Joaquin Valley during the California Regional PM10/PM2.5 Air Quality Study (CRPAQS) winter campaign from December 15, 2000 to February 3, 2001. PM2.5 filter samples were collected concurrently at both sites with Sequential Filter Samplers (SFS). MOUDI nitrate (NO3) concentrations reached 66 μg/m3 on January 6, 2001 during the 1000–1600 PST (GMT-8) period. Pair-wise comparisons between PM2.5 MOUDI and SFS concentrations revealed high correlations at the Angiola site (r > 0.93) but more variability (r < 0.85) at the Fresno site for NO3, sulfate (SO4=), and ammonium (NH4+). Correlations were higher at Fresno (r > 0.87) than at Angiola (r < 0.7) for organic carbon (OC), elemental carbon (EC), and total carbon (TC). NO3 and SO4= size distributions in Fresno were multi-modal and wider than the uni-modal distributions observed at Angiola. Geometric mean diameters (GMD) were smaller for OC and EC than for NO3 and SO4= at both sites. OC and EC were more concentrated on the lowest MOUDI stage (0.056 µm) at Angiola than at Fresno. The NO3 GMD increased from 0.97 to 1.02 µm as the NO3 concentration at Angiola increased from 43 to 66 µg m− 3 during a PM2.5 episode from January 4–7, 2001. There was a direct relationship between GMD and NO3 and SO4= concentrations at Angiola but no such relationships for OC or EC. This demonstrates that secondary aerosol formation increases both concentration and particle size for the rural California environment.  相似文献   

17.
The concentrations of PM10, PM2.5 and their water-soluble ionic species were determined for the samples collected during January to December, 2007 at New Delhi (28.63° N, 77.18° E), India. The annual mean PM10 and PM2.5 concentrations (± standard deviation) were about 219 (± 84) and 97 (±56) μgm−3 respectively, about twice the prescribed Indian National Ambient Air Quality Standards values. The monthly average ratio of PM2.5/PM10 varied between 0.18 (June) and 0.86 (February) with an annual mean of ∼0.48 (±0.2), suggesting the dominance of coarser in summer and fine size particles in winter. The difference between the concentrations of PM10 and PM2.5, is deemed as the contribution of the coarse fraction (PM10−2.5). The analyzed coarse fractions mainly composed of secondary inorganic aerosols species (16.0 μgm−3, 13.07%), mineral matter (12.32 μgm−3, 10.06%) and salt particles (4.92 μgm−3, 4.02%). PM2.5 are mainly made up of undetermined fractions (39.46 μgm−3, 40.9%), secondary inorganic aerosols (26.15 μgm−3, 27.1%), salt aerosols (22.48 μgm−3, 23.3%) and mineral matter (8.41 μgm−3, 8.7%). The black carbon aerosols concentrations measured at a nearby (∼300 m) location to aerosol sampling site, registered an annual mean of ∼14 (±12) μgm−3, which is significantly large compared to those observed at other locations in India. The source identifications are made for the ionic species in PM10 and PM2.5. The results are discussed by way of correlations and factor analyses. The significant correlations of Cl, SO42−, K+, Na+, Ca2+, NO3 and Mg2+ with PM2.5 on one hand and Mg2+ with PM10 on the other suggest the dominance of anthropogenic and soil origin aerosols in Delhi.  相似文献   

18.
2018年1月,利用颗粒物采样器采集武汉市大气PM2.5样品并进行水溶性无机离子(F-、Cl-、NO3-、SO42-、Na+、NH4+、K+、Mg2+、Ca2+)的分析.结果表明,NO3-、SO42-、NH4+是PM2.5中最主要的3种水溶性无机离子,除Mg2+与Ca2+外,PM2.5与WSⅡs (水溶性无机离子)之间的相关性显著,且移动源贡献占主导地位.阴阳离子平衡表明武汉市冬季灰霾期PM2.5呈中性或弱酸性.通过混合单粒子拉格朗日综合轨迹模式模拟并采用分层聚类得出了4种主要的后向气流轨迹及相应的PM2.5和水溶性离子浓度,结果表明区域传输对此次灰霾期影响较大.  相似文献   

19.
The heterogeneous interaction of nitrogen dioxide with ammonium chloride was investigated in a molecular diffusion tube experiment at 295–335 K and interpreted using Monte Carlo trajectory calculations. The surface residence time (τsurf) of NO2 on NH4Cl is equal to 15 μs at 295 K, increases with temperature up to 323 K (τsurf = 45 μs) and probably decreases beyond 323 K. The same experiment also yields uptake coefficients, γ, which are derived from the absolute number of surviving molecules effusing out of the diffusion tube. The rate of uptake of NO2 on NH4Cl followed a rate law first order in [NO2] and the uptake coefficient γ is equal to 7 × 10−5 at 295 K, increases with temperature up to 323 K (γ = 2.1 × 10−4) and probably decreases beyond 323 K. Nitrous acid, water and nitrogen were detected as products. From these products, it is concluded that the reaction of NO2 with NH4Cl is a reverse disproportionation reaction where two moles of NO2 result in ammonium nitrite, NH4NO2, as an intermediate, and nitryl chloride, NO2Cl. NH4NO2 decomposes in two pathways, one to nitrous acid, HONO and NH3, the other to nitrogen and water. The branching ratio for the production of HONO + NH3 to that of N2 + H2O is approximately 20 at 298 K and increases with increasing temperature.  相似文献   

20.
本文利用2014年全年北京市12个空气质量监测站的逐小时PM_(2.5)地面观测资料,以及Terra卫星和Aqua卫星的MODIS 3 km气溶胶光学厚度(AOD)产品,分析了地面PM_(2.5)和两颗卫星AOD的时空分布特征,并在时空匹配的基础上,建立了AOD与PM_(2.5)浓度之间的回归模型。结果表明:PM_(2.5)浓度在城区高、郊区低,最低值位于定陵站,城区站和郊区站的逐时PM_(2.5)浓度的日变化分别呈"双峰型"和"单峰型";两颗卫星AOD数值也均是城区高、郊区低,沿山区的边界有明显的AOD梯度,且城区上午Terra卫星的AOD高于下午Aqua卫星的AOD,而郊区上、下午的AOD基本相同;Aqua卫星AOD与PM_(2.5)的确定系数(R2)较Terra卫星AOD与PM_(2.5)的确定系数平均高0.11,且城区站点两颗卫星AOD与PM_(2.5)相关性均较郊区站点AOD与PM_(2.5)相关性偏高;综合来看,Aqua卫星的AOD与城区的PM_(2.5)相关系数最高,即Aqua卫星的AOD更适于监测和反演城区地面的PM_(2.5)。  相似文献   

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