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1.
A comprehensive study on the chemical compositions of rainwater was carried out from June 2007 to December 2008 in Guiyang, a city located on the acid rain control zone of southwest China. All samples were analyzed for pH, major anions (F−, Cl−, NO3−, SO42−), major cations (K+, Na+, Ca2+, Mg2+, NH4+), Sr2+ and Sr isotope. The pH increase is due to the result of neutralization caused by the alkaline dust which contain large amount of CaCO3. It was observed that Ca2+ was the most abundant cation with a volume-weighted mean (VWM) value of 217.6 μeq/L (52.7–1928 μeq/L), accounting for 66% (39%–88%) of the total cations. SO42− was the most abundant anion with VWM value of 237.8 μeq/L (49.6-1643 μeq/L). SO42− and NO3− were dominant among the anions, accounting for 66%–97% of the total measured anions. The Sr concentrations vary from 0.01 to 0.92 μmol/L, and strontium isotopic ratios vary in the range of 0.707684–0.710094, with an average of 0.708092. The elements ratios and the 87Sr/86Sr ratios showed that the solutes of rainwater mainly come from weathering of carbonate and secondary dust input. Moreover, urbanization results in the calcium-rich dust increased and the high concentrations of alkaline ions (mainly Ca2+) have played an important role to neutralize the acidity of rainwater, leading to the increase of arithmetic pH mean value by 0.5 units since 2002. It is worth noting that the emission of SO2 and NOx from the automobile exhaust is increasing and is becoming another important precursor of acid rain now.  相似文献   

2.
In this paper warm cloud microphysical parameters including cloud droplet number concentration (Nc), liquid water content (ql) and effective radius (re) from 75 flights around the Beijing area during 2005 and 2006 are summarized. Average Nc (cm− 3) for Cu, Sc, Ac, As and Ns are 376 ± 290, 257 ± 226, 147 ± 112, 60 ± 35 and 60 ± 84, respectively. Many records of high Nc above 1000 cm− 3 are observed. The large standard deviations indicate a large variation of Nc and ql in this region. The maxima of ql reach 1.4 g m− 3 in Cu and 1.0 g m− 3 in Sc, respectively. Different parameterizations of effective radius are examined with the in-situ data in this area. There are different ways to obtain the prefactor representing the relationship between effective radius and mean volume radius. Significant systematic errors are found to be at the large sizes when the prefactor is expressed with relative dispersion under the Gamma Distribution. Fixed prefactor of 1, which was widely used, even produces much larger error. A prefactor of 1.22 is found to be better than the former two methods by fitting with the observed data. The effective radius is further parameterized as functions of mean volume radius, liquid water content and cloud droplet number concentration. We suggest that the effective radius can be parameterized as re,p ≈ 1.20rv + 0.22–1.28/rv2, which is a practical and more accurate scheme without too much computation complexity.  相似文献   

3.
The changing chemical composition of cloud water and precipitation in the Western Sudety Mountains are discussed against the background of air-pollution changes in the Black Triangle since the 1980s until September 2004. A marked reduction of sulphur dioxide emissions between the early 1990's and the present (from almost 2 million tons to around 0.2 million tons) has been observed, with a substantial decline of sulphate and hydrogen concentration in cloud water (SO42− from more than 200 to around 70 μmol l− 1; H+ from 150 to 50 μmol l− 1) and precipitation (SO42− from around 80 to 20–30 μmol l− 1; H+ from around 60 to 10–15 μmol l− 1) samples. At some sites, where fog/cloud becomes the major source of pollutants, deposition hot spots are still observed where, for example, nitrogen deposition can exceed 20 times the relevant critical load. The results show that monitoring of cloud water chemistry can be a sensitive indicator of pollutant emissions.  相似文献   

4.
During the spring of 2005, the total particle concentrations and the submicron aerosol size distributions were measured on board the research vessel over the south sea of Korea and the Korean sector of the Yellow Sea. Similar measurements were made over the East China Sea in autumn 2005. The aerosol properties varied dynamically according to the meteorological conditions, the proximity to the land masses and the air mass back trajectories. The average total particle concentration was the lowest over the East China Sea, 4335 ± 2736 cm− 3, but the instantaneous minimum, 837 cm− 3, for the entire ship measurement was recorded during the Yellow Sea cruise. There was also a long (more than 6 h) stretch of low total particle concentrations that fell as low as 1025 cm− 3 during the East China Sea cruise when the ship was the farthest from the shores and the air mass back trajectories resided long hours over the sea. These observations lead to the suggestion of ~ 1000 cm− 3 as the background total particle concentration over the marine boundary layer in the studied region of the Yellow Sea and the East China Sea, implying significant anthropogenic influence even for the background value. In the mean time, average aerosol size distributions were unimodal and the mode diameter ranged between 52 and 86 nm, excluding the fog periods, which suggests that the aerosols measured in this study experienced relatively less aging processes within the marine boundary layer.  相似文献   

5.
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   

6.
A total of 48 precipitation samples have been collected from individual precipitation events at the Nam Co Monitoring and Research Station for Multisphere Interactions (Nam Co Station, 30°47′N, 90°58′E; 4730 m a.s.l) located in the central Tibetan Plateau from August 2005 to August 2006. All samples were analyzed for major cations (NH4+, Na+, K+, Ca2+ and Mg2+) and anions (Cl−, NO3− and SO42−), conductivity and pH. Precipitation pH values ranged from 6.03 to 7.38 with an average value of 6.59. The high pH is due to large inputs of crustal aerosols in the atmosphere, which contain a large fraction of carbonate. Ca2+ is the dominant cation in precipitation with an average value of 65.58 μeq L− 1 (4.91–301.41 μeq L− 1), accounting for 54% of the total cations in precipitation. HCO3− is the predominant anion, accounting for 62% of the total anions. When compared with data from a snow pit in the Zhadang Glacier 50 km away (5800 m a.s.l), major ion concentration in precipitation at the Nam Co Station is much higher due to local aerosol inputs. Correlation and empirical orthogonal function (EOF) analysis indicate that regional crustal aerosols and species from combustion emissions of residents are the major sources for these ions, lake salt aerosols from the Nam Co nearby and regional mineral aerosols from dry lake sediments are secondary sources, and sea salt contribution is the least due to the long distance transport.  相似文献   

7.
Black carbon relationships with emissions and meteorology in Xi'an, China   总被引：4，自引：0，他引：4  
Aerosol black carbon (BC) was measured every 5 min at Xi'an, China from September 2003 to August 2005. Daily BC concentrations ranged from 2 to 65 μg m− 3, averaging 14.7 ± 9.5 μg m− 3 and displayed clear summer minima and winter maxima. BC typically peaked between 0800 and 1000 LST and again between 2000 and 2200 LST, corresponding with morning and evening traffic combined with nighttime residential cooking and heating. The nocturnal peak was especially evident in winter, when more domestic heating is used and pollutant-trapping surface-inversions form earlier than in summer. BC frequency distributions the most commonly occurring concentrations occurred between 5 and 10 μg m− 3 in all four seasons. BC ranged from 1.6% and 15.6%, and averaged 8.3% of PM2.5. A clear inverse relationship between BC and wind speed (WS) was found when WS was below 2.5 to 3.0 m s− 1, implying a local origin for BC. Mixed layer depths (MLDs) were shallower during BC episodes compared to cleaner conditions.  相似文献   

8.
To further investigate the influence of cloud base temperature, updraft velocity and precipitation particle constitution on cloud electrification, five thunderstorms in various regions of China were simulated by using the three-dimensional compressible hailstorm numerical model including inductive and non-inductive charging mechanisms. The results indicate that changes of cloud base temperature have an influence on the initial electrification. Comparison of the above cases shows that in the case of warm cloud base and moderate updraft velocity (< 20 m s−  1), active electrification occurred below the − 10 °C level before moving upward to the − 20 °C level. In contrast, when cloud base is cold and updraft velocity is intensive, the main charging region is at the − 20 °C or even higher level. In that case, the vertical extent of the main negative charge region becomes larger with the increase of cloud base temperature. Apart from the main dipolar or tripolar charge structure, some smaller charge regions with relatively high values of charge density may also appear. Frozen drops, originating mainly from supercooled raindrops, mainly get electrified through charging interactions with snow at or below the − 20 °C level. They are responsible for the negative charge region near the melting level at the initial stage of precipitation if there is a large supercooled raindrop content. Non-inductive charging during hail-snow collisions is rather weak, resulting in the charge density on hail of no more than − 0.01 nC m− 3.  相似文献   

9.
Deposition of atmospheric particulate PCBs in suburban site of Turkey   总被引：2，自引：1，他引：2  
Dry deposition and air concentration samples were collected from July 2004 to May 2005 at a suburban site in Turkey. A water surface sampler (WSS) was used to measure directly the dry deposition flux of particulate polychlorinated biphenyls (PCBs) while a high volume air sampler (HVAS) was employed to collect air samples. Particulate PCB concentrations accounted for 15% of total PCBs (gas + particle phase) at the site. The overall particulate phase PCB flux ranged from 2 to 160 ng m− 2 d− 1 with an average of 46.3 ± 40.6 ng m− 2 d− 1. Forty one PCB congeners were targeted in the samples while twenty one congeners were found to be higher than detection limits in deposition samples. Fluxes for homolog groups ranged between 0.9 (7-CBs) and 21.0 (3-CBs) ng m− 2 d− 1. Measured dry deposition fluxes were lower than the ones usually reported for urban sites. Average PCB dry deposition velocity, calculated using flux values and concurrently measured atmospheric concentrations, was 1.26 ± 1.86 cm s− 1 depended on size distribution of particles, atmospheric PCB concentrations and meteorological conditions.  相似文献   

10.
We present results of direct aerosol radiative forcing over a French Mediterranean coastal zone based on one year of continuous observations of aerosol optical properties during 2005–2006. Monthly-mean aerosol optical depth at 440 nm ranged between 0.1 and 0.34, with high Angstrom coefficient (α > 1.2). The single scattering albedo (at 525 nm) estimated at the surface ranged between 0.7 and 0.8, indicating significant absorption. The presence of aerosols over the Mediterranean zone during summer decreases the shortwave radiation reaching the surface by as much as 26 ± 3.9 W m− 2, and increases the top of the atmosphere reflected radiation by as much as 5.2 ± 1.0 W m− 2. The shortwave atmospheric absorption translates to an atmospheric heating of 2.5 to 4.6 K day− 1. Concerted efforts are needed for investigating the possible impact of the increase in heating rate on the maintenance of heat-waves frequently occurring over this coastal region during summer time.  相似文献   

11.
In the present study, the wet and dry depositions of particulate NO3−, SO42−, Cl− and NH4+ were measured using a wet/dry sampler as a surrogate surface. Gas phase compounds of nitrogen, sulfur and chloride (HNO3, NH3, SO2 and HCl) were measured by an annular denuder system (ADS) equipped with a back up filter for the collection of particles with diameter ≤ 5 μm. Ambient concentrations of NO, NO2 and SO2 were also taken into consideration. Sampling was conducted at an urban site in the center of the city of Thessaloniki, northern Greece. The presence of the aerosol species was examined by cold/warm period and the possible compounds in dry deposits were also considered. Dry deposition fluxes were found to be well correlated with ambient particle concentrations in order to be used for the calculation of particle deposition velocity. Average particulate deposition velocities calculated were 0.36, 0.20, 0.20 and 0.10 cm s− 1 for Cl−, NO3−, SO42− and NH4+, respectively. Total dry deposition fluxes (gas and particles) were estimated at 3.24 kg ha− 1 year− 1 for chloride (HCl + p-Cl), 9.97 kg ha− 1 year− 1 for nitrogen oxidized (NO + NO2 + HNO3 + p-NO3), 5.32 kg ha− 1 year− 1 for nitrogen reduced (NH3 + p-NH4) and 15.77 kg ha− 1 year− 1 for sulfur (SO2 + p-SO4). 70–90% total dry deposition was due to gaseous species deposition. The contribution of dry deposition to the total (wet + dry) was at the level of 60–70% for sulfur and nitrogen (oxidized and reduced), whereas dry chloride deposition contributed 35% to the total. The dry-to-wet deposition ratio of all the studied species was found to be significantly associated with the precipitation amount, with nitrogen species being better and higher correlated. Wet, dry and total depositions measured in Thessaloniki, were compared with other countries of Europe, US and Asia.  相似文献   

12.
Methanesulfonate (MS–) and non-sea-salt sulfate (nss-SO 4 2– ), two of the major oxidation products of atmospheric dimethylsulfide (DMS), have been continuously measured in rainwater at three remote islands in the Southern Indian Ocean: Amsterdam since 1991, Crozet since 1992, and Kerguelen since 1993. The annual volume weighted mean (VWM) concentrations of nss-SO 4 2– in rainwater were 3.19, 3.04 and 4.57 eq l–1 at Amsterdam, Crozet, and Kerguelen, respectively while the VWM of MS– were 0.24, 0.15 and 0.30 eq l–1, respectively. At all three islands, MS– presented a well-distinguished seasonal variation with a maximum during summer whereas the seasonal variation of nss-SO 4 2– was less pronounced, possibly due to the increased anthropogenic influence during the winter period. Furthermore, MS– presented significant interannual variations, in particular at Amsterdam and Crozet, which is closely related to the sea-surface temperature (SST) anomalies). Finally, the nss-SO 4 2– deposition at Crozet Island presented a decreasing interannual trend, reflecting probably reductions in sulfur emissions from Southern Africa. On the contrary no interannual tendency was observed in the nss-SO 4 2– concentrations at Amsterdam Island, indicating that the biogeochemical sulfur cycle at this area is mainly influenced by biogenic emissions.  相似文献   

13.
The pH variation and chemical characteristics of rainwater were investigated from January 2006 to December 2006 at an urban site of Guangzhou, South China. The rainwater was typically acidic with a volume-weighted mean pH value of 4.49, which ranged from 3.52 to 6.28. The volume-weighted mean equivalent concentration of components followed the order: SO42− > Ca2+ > Cl− > NH4+ > Na+ > NO3− > K+ > Mg2+ > F−, indicating that SO42−, Cl− and NO3− were the main anions, while Ca2+ and NH4+, were the main cations. Ca2+ and NH4+ were major neutralization constituents of the precipitation. Furthermore, correlation analysis and principal component analysis method were performed to identify possible common sources of major ions. Sources of the major ions were assessed based on enrichment factor method.  相似文献   

14.
Gas and particle phase concentrations of atmospheric polychlorinated biphenyls (PCBs) were measured at an urban/industrial site in the city of Bursa, Turkey. PCB concentration levels were presented between July 2004 and May 2005. Average particle and gas phase concentrations of individual PCB congeners ranged from 0.08 (PCB-183) to 6.86 (PCB-49) pg m− 3 and from 0.01 (PCB-209) to 47.2 (PCB-33) pg m− 3, respectively. The mean concentration of total (gas + particle) PCBs varied between 24.27 and 666.21 pg m− 3 with an average of 287.27 ± 174.80 pg m− 3. PCB concentrations at the sampling site were higher than the concentrations reported at non-urban sites. PCBs partitioned between gas and particle phases and the partitioning was examined according to different approaches such as logKp–logPLo, logKp–logKOA and the Junge–Pankow model. In order to present possible interactions, a correlation matrix based on PCB congeners and meteorological parameters was constructed. Application of the Clausius–Clapeyron equation yielded a low slope value indicating possible emissions from local and regional sources originating mainly from urban/industrial areas, landfill and waste incineration plant. Then, likely dry deposition fluxes were estimated depending on reported dry deposition velocity and atmospheric concentration values.  相似文献   

15.
This paper presents the development of a simple and precise analytical method for the determination of nitrogen dioxide in ambient air. In this method nitrogen dioxide is determined in the form of nitrite. The determination of nitrogen dioxide needs no reagents except for a solution of sodium hydroxide mixed with sodium arsenite (NaOH–Na2As2O3) which is used as an absorbing reagent for trapping the nitrogen dioxide from the atmosphere in the form of nitrite, i.e., a prior analysis step. The determination of submicrogram levels of nitrogen dioxide is based on the selection of a strong and sharp quantitative analytical peak at 1380 cm− 1 using diffuse reflectance infrared spectroscopy (DRS-FTIR). The limit of detection (LOD) and the limit of quantification of the method are found to be 0.008 μg g− 1 NO2− and 0.05 μg g− 1 NO2−, respectively. The precision in terms of standard deviation and relative standard deviation value at a level of 2 μg NO2− / 0.1 g KBr for n = 10 is found to be 0.036 μg NO2− and 1.8%, respectively. The relative standard deviation (n = 10) for the determination of nitrogen dioxide in ambient air was observed to be in the range 2.6–3.8%. The method proposed is time-saving and eliminates the slow and cumbersome steps of pH maintenance of the reaction mixture and color formation of the EPA recommended spectrophotometric and other methods for quantitative determination of nitrogen dioxide.  相似文献   

16.
Normal alkanes and PAHs in atmospheric PM10 aerosols collected during 2008 winter and spring in Baoji, a mid-scale inland city of China, were determined on a molecular level. Concentrations of n-alkanes ranged from 232 to 3583 ng/m3 with an average of 1733 ng/m3 in winter and from 124 to 1160 ng/m3 with an average of 449 ng/m3 in spring, while PAHs in the PM10 samples were 594 ± 405 and 128 ± 82 ng/m3 in the two seasons. Molecular compositions showed that CPI (odd/even) values of n-alkanes were close to unity for all the samples especially in winter, and diagnostic ratios of PAHs (e.g., Phe/(Phe + Ant), CPAH/ΣPAHs and IcdP/(IcdP + BghiP)) were found similar to those in coal burning smoke with a strong linear relationship (R2 ≥ 0.85) between PAHs and fossil fuel derived n-alkanes, demonstrating that coal burning is the main source of n-alkanes and PAHs in the city, especially in winter due to house heating. Concentrations of the determined compounds in Baoji are much higher than those in Chinese mega-cities, suggesting that air pollution in small cities in the country is more serious and need more attention.  相似文献   

17.
The formation of dew, deposition of frost and accumulation of snow mainly on the upper domes of a non-ventilated net radiometer seriously affect the measurement of available energy (net radiation). Net radiometers measure radiation, and energy balances and are widely used for estimation of evapotranspiration throughout the world. To study the effects of dew, frost, and snow on a non-ventilated net radiometer, a radiation station was set up which uses 2 CM21 Kipp & Zonen pyranometers (one inverted), 2 CG1 Kipp & Zonen pyrgeometers (one inverted), along with a Q7.1 net radiometer (Radiation & Energy Balance Systems, Inc.; REBS) in a semi-arid mountainous valley in Logan, Utah, U.S.A. The pyranometers and pyrgeometers were ventilated using 4 CV2 Kipp & Zonen ventilation systems. The net radiometer was not ventilated. The ventilation of pyranometers and pyrgeometers prevents dew and frost deposition and snow accumulation which otherwise would disturb measurements. All sensors were installed at about 3.0 m above the ground, which was covered with natural vegetation during the growing season (May–September). The incoming and outgoing solar or shortwave radiation, the incoming (atmospheric) and outgoing (terrestrial) longwave radiation, and the net radiation have been continuously measured by pyranometers, pyrgeometers and a net radiometer, respectively, since 1995. These parameters have been measured every 2 s and averaged into 20 min. To evaluate the effects of dew, frost, and snow, three days were chosen: 26 April 2004 with early morning dew, 6 January 2005 with an early morning frost, and the snowy day of 24 February 2005. Dew formation, frost deposition, and snow accumulation occurred mainly on the upper dome of the non-ventilated Q7.1 net radiometer on the related days, while the ventilated Kipp & Zonen system was free of dew, frost and snow. Net radiation measured by the non-ventilated net radiometer Rn,unvent. during dew and frost periods of the above-mentioned days was greater than ventilated ones Rn,vent. (− 0.2 MJ m− 2 vs. − 0.8 MJ m− 2 during almost 4 h on 26 April 2004, and − 0.2 MJ m− 2 vs. − 0.7 MJ m− 2 during almost 6.5 h on 6 January 2005). The reason for higher reading by the non-ventilated net radiometer during dew and frost periods was due to emission of additional longwave radiation from water and ice crystals formed mainly on the upper dome of the Q7.1 net radiometer. In contrast, during the snowy day of 24 February 2005, the Rn,unvent. was less than Rn,vent. (− 4.00 MJ m− 2 vs. 0.77 MJ m− 2, mainly from sunrise to sunset). The extremely low Rn,unvent. measured by the non-ventilated net radiometer on 24 February 2005 is due to blocking of the incoming solar radiation (mainly diffuse radiation) by the snow-covered upper dome.  相似文献   

18.
Using a high-speed camera system and two electric field antenna systems, we have documented the initial processes of an altitude-triggered negative lightning (ATNL). The optical records clearly show that ATNL begins with the inception and propagation of an upward positive leader (UPL) and then a simultaneous propagation of UPL and downward negative leader (DNL), known as the bidirectional leader process, follows. Based on the optical records, it is inferred that (1) the triggering height is about 371 m; (2) the two-dimensional (2D) propagation speed of the UPL in its inception phase is about 3.8–5.5 × 104 m s− 1 during its propagation from about 393 to 452 m above the ground; (3) the grey levels of the DNL are about one order of magnitude higher than that of the UPL in their inception phase; (4) a discharge phenomenon propagating along the elevated triggering wire part of the lightning channel occurs after the mini-return stroke (MRS), with a 2D propagation speed of about 1.6–2.0 × 105 m s− 1. Combined with the simultaneous electric field change records, it is further inferred that (1) the UPL incepts about 932 μs earlier than the unstable DNL and about 4.1 ms earlier than the stable DNL; (2) the unstable DNL propagates downward intermittently three times with a time interval of about 1 ms, and each propagation contains a different number of steps with an average step length of about 7 m; (3) the stable DNL incepts at the tip of the unstable one, with a 2D propagation speed of about 1.9 × 105 m s− 1, an average step length of about 3 m, and a stepping time interval varying from 6 to 31 µs with a mean value of 15 µs.  相似文献   

19.
The potential resources on the ion-stimulated syntheses effects of aerosol particles of lower troposphere in test sites in the arctic, mountain, arid and forest areas as the function of irradiation time and gas-precursor concentration were experimentally and theoretically evaluated. The dust-free outdoor air was irradiated with an ionization current of 10− 6 A by α-rays from isotope 239Pu. The total output of radiolytic aerosols (RA) with a diameter of 3–1000 nm was found to be 0.05–0.1 molecules per 1 eV of absorbed radiation, while the physical upper limit is 0.25–0.4 molecules/eV. In an interval of exposition time from 6 to 800 s (adsorbed energy is 3 · 1012–1014 eV/cm3) the RA mass concentration at different sites was increased from 1–10 to 50–500 μg/m3. According to the liquid chromatography data the major RA material is the H2O/HNO3 solution with acid concentration  25%. The used physical model presents new aerosols as a product from small and intermediate ion association through formation of neutral clusters and describes adequately some of the peculiarities in field experiment data. Introducing SO2, NH3, and also hydrochloric, nitric and sulphuric acid vapours with concentration 0.1–1 mg/m3 in the irradiated air stimulated an increase of mass aerosol concentration by a factor of 8–30. The mean size also decreased by a factor of 3–5. These facts allowed us to expect that the chemical composition of radiolytic aerosols generated in outdoor air would noticeably differ after addition of the gas-precursors.  相似文献   

20.
The main objective of this study is to investigate the chemical characteristics of biomass burning aerosol and its impact on regional air quality during an agricultural waste burning period in early summer in the rural areas of Korea. A 12-h integrated intensive sampling of biomass burning aerosol in the fine and coarse modes was conducted on 2–20 June 2003 in Gwangju, Korea. The collected samples were analyzed for concentrations of mass, ionic, elemental, and carbonaceous species. Average concentrations of fine and coarse mass were measured to be 67.9 and 18.7 μg m− 3 during the biomass burning period, 41.9 and 18.8 μg m− 3 during the haze period, and 35.6 and 13.3 μg m− 3 during the normal period, respectively. An exceptionally high PM2.5 concentration of 110.3 μg m− 3 with a PM2.5/PM10 ratio of 0.79 was observed on 6 June 2003 during the biomass burning period. The potassium ratio method was used to identify biomass burning samples. The average ratio of potassium in the fine mode to the coarse mode (FK/CK) was 23.8 during the biomass burning period, 6.0 during the haze period, and 4.7 during the normal period, respectively. A FK/CK ratio above 9.2 was considered a criterion for biomass burning event in this study. Particulate matter from the open field burning of agricultural waste has an adverse impact on visibility, human health, and regional air quality.  相似文献   

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