WorldWideScience

Sample records for carbonaceous aerosol particles

  1. Laboratory Experiments and Instrument Intercomparison Studies of Carbonaceous Aerosol Particles

    Energy Technology Data Exchange (ETDEWEB)

    Davidovits, Paul [Boston College, Chestnut Hill, MA (United States)

    2015-10-20

    Aerosols containing black carbon (and some specific types of organic particulate matter) directly absorb incoming light, heating the atmosphere. In addition, all aerosol particles backscatter solar light, leading to a net-cooling effect. Indirect effects involve hydrophilic aerosols, which serve as cloud condensation nuclei (CCN) that affect cloud cover and cloud stability, impacting both atmospheric radiation balance and precipitation patterns. At night, all clouds produce local warming, but overall clouds exert a net-cooling effect on the Earth. The effect of aerosol radiative forcing on climate may be as large as that of the greenhouse gases, but predominantly opposite in sign and much more uncertain. The uncertainties in the representation of aerosol interactions in climate models makes it problematic to use model projections to guide energy policy. The objective of our program is to reduce the uncertainties in the aerosol radiative forcing in the two areas highlighted in the ASR Science and Program Plan. That is, (1) addressing the direct effect by correlating particle chemistry and morphology with particle optical properties (i.e. absorption, scattering, extinction), and (2) addressing the indirect effect by correlating particle hygroscopicity and CCN activity with particle size, chemistry, and morphology. In this connection we are systematically studying particle formation, oxidation, and the effects of particle coating. The work is specifically focused on carbonaceous particles where the uncertainties in the climate relevant properties are the highest. The ongoing work consists of laboratory experiments and related instrument inter-comparison studies both coordinated with field and modeling studies, with the aim of providing reliable data to represent aerosol processes in climate models. The work is performed in the aerosol laboratory at Boston College. At the center of our laboratory setup are two main sources for the production of aerosol particles: (a

  2. Carbonaceous aerosol particles from common vegetation in the Grand Canyon

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    Hallock, K.A.; Mazurek, M.A. [Brookhaven National Lab., Upton, NY (United States); Cass, G.R. [California Inst. of Tech., Pasadena, CA (United States). Dept. of Environmental Engineering Science

    1992-05-01

    The problem of visibility reduction in the Grand Canyon due to fine organic aerosol particles in the atmosphere has become an area of increased environmental concern. Aerosol particles can be derived from many emission sources. In this report, we focus on identifying organic aerosols derived from common vegetation in the Grand Canyon. These aerosols are expected to be significant contributors to the total atmospheric organic aerosol content. Aerosol samples from living vegetation were collected by resuspension of surface wax and resin components liberated from the leaves of vegetation common to areas of the Grand Canyon. The samples were analyzed using high-resolution gas chromatography/mass spectrometry (GC/MS). Probable identification of compounds was made by comparison of sample spectra with National Institute of Standards and Technology (NIST) mass spectral references and positive identification of compounds was made when possible by comparison with authentic standards as well as NIST references. Using these references, we have been able to positively identify the presence of n-alkane and n-alkanoic acid homolog series in the surface waxes of the vegetation sampled. Several monoterpenes, sesquiterpenes, and diterpenes were identified also as possible biogenic aerosols which may contribute to the total organic aerosol abundance leading to visibility reduction in the Grand Canyon.

  3. Carbonaceous aerosol particles from common vegetation in the Grand Canyon

    International Nuclear Information System (INIS)

    The problem of visibility reduction in the Grand Canyon due to fine organic aerosol particles in the atmosphere has become an area of increased environmental concern. Aerosol particles can be derived from many emission sources. In this report, we focus on identifying organic aerosols derived from common vegetation in the Grand Canyon. These aerosols are expected to be significant contributors to the total atmospheric organic aerosol content. Aerosol samples from living vegetation were collected by resuspension of surface wax and resin components liberated from the leaves of vegetation common to areas of the Grand Canyon. The samples were analyzed using high-resolution gas chromatography/mass spectrometry (GC/MS). Probable identification of compounds was made by comparison of sample spectra with National Institute of Standards and Technology (NIST) mass spectral references and positive identification of compounds was made when possible by comparison with authentic standards as well as NIST references. Using these references, we have been able to positively identify the presence of n-alkane and n-alkanoic acid homolog series in the surface waxes of the vegetation sampled. Several monoterpenes, sesquiterpenes, and diterpenes were identified also as possible biogenic aerosols which may contribute to the total organic aerosol abundance leading to visibility reduction in the Grand Canyon

  4. Isotope source apportionment of carbonaceous aerosol as a function of particle size and thermal refractiveness

    Science.gov (United States)

    Masalaite, Agne; Holzinger, Rupert; Remeikis, Vidmantas; Röckmann, Thomas; Dusek, Ulrike

    2016-04-01

    The stable carbon isotopes can be used to get information about sources and processing of carbonaceous aerosol. We will present results from source apportionment of carbonaceous aerosol as a function of particle size thermal refractiveness. Separate source apportionment for particles smaller than 200 nm and for different carbon volatility classes are rarely reported and give new insights into aerosol sources in the urban environment. Stable carbon isotope ratios were measured for the organic carbon (OC) fraction and total carbon (TC) of MOUDI impactor samples that were collected on a coastal site (Lithuania) during the winter 2012 and in the city of Vilnius (Lithuania) during the winter of 2009. The 11 impactor stages spanned a size range from 0.056 to 18 μm, but only the 6 stages in the submicron range were analysed. The δ13C values of bulk total carbon (δ13CTC) were determined with an elemental analyser (Flash EA 1112) coupled with an isotope ratio mass spectrometer (Thermo Finnigan Delta Plus Advantage) (EA - IRMS). Meanwhile δ13COC was measured using thermal-desorption isotope ratio mass spectrometry (IRMS) system. This allows a rough separation of the more volatile OC fraction (desorbed in the oven of IRMS up to 250 0C) from the more refractory fraction (desorbed up to 400 0C). In this study we investigated the composition of organic aerosol desorbed from filter samples at different temperatures using the thermal-desorption proton-transfer-reaction mass spectrometry (TD-PTR-MS) technique. During winter-time in Lithuania we expect photochemistry and biogenic emissions to be of minor importance. The main sources of aerosol carbon should be fossil fuel and biomass combustion. In both sites, the coastal and the urban site, δ13C measurements give a clear indication that the source contributions differ for small and large particles. Small particles NWO grants Nr. 820.01.001, and 834.08.002).

  5. Composition of carbonaceous smoke particles from prescribed burning of a Canadian boreal forest: 1. Organic aerosol characterization by gas chromatography

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    Mazurek, M.A.; Laterza, C.; Newman, L.; Daum, P. [Brookhaven National Lab., Upton, NY (United States); Cofer, W.R. III; Levine, J.S. [National Aeronautics and Space Administration, Hampton, VA (United States). Langley Research Center; Winstead, E.L. [Science Applications International Corporation, Hampton, VA (United States)

    1995-06-01

    In this study we examine the molecular organic constituents (C8 to C40 lipid compounds) collected as smoke particles from a Canadian boreal forest prescribed burn. Of special interest are (1) the molecular identity of polar organic aerosols, and (2) the amount of polar organic matter relative to the total mass of aerosol particulate carbon. Organic extracts of smoke aerosol particles show complex distributions of the lipid compounds when analyzed by capillary gas chromatography/mass spectrometry. The molecular constituents present as smoke aerosol are grouped into non-polar (hydrocarbons) and polar {minus}2 oxygen atoms) subtractions. The dominant chemical species found in the boreal forest smoke aerosol are unaltered resin compounds (C20 terpenes) which are abundant in unburned conifer wood, plus thermally altered wood lignins and other polar aromatic hydrocarbons. Our results show that smoke aerosols contain molecular tracers which are related to the biofuel consumed. These smoke tracers can be related structurally back to the consumed softwood and hardwood vegetation. In addition, combustion of boreal forest materials produces smoke aerosol particles that are both oxygen-rich and chemically complex, yielding a carbonaceous aerosol matrix that is enriched in polar substances. As a consequence, emissions of carbonaceous smoke particles from large-scale combustion of boreal forest land may have a disproportionate effect on regional atmospheric chemistry and on cloud microphysical processes.

  6. Quantitative determination of carbonaceous particle mixing state in Paris using single particle mass spectrometer and aerosol mass spectrometer measurements

    Science.gov (United States)

    Healy, R. M.; Sciare, J.; Poulain, L.; Crippa, M.; Wiedensohler, A.; Prévôt, A. S. H.; Baltensperger, U.; Sarda-Estève, R.; McGuire, M. L.; Jeong, C.-H.; McGillicuddy, E.; O'Connor, I. P.; Sodeau, J. R.; Evans, G. J.; Wenger, J. C.

    2013-04-01

    Single particle mixing state information can be a powerful tool for assessing the relative impact of local and regional sources of ambient particulate matter in urban environments. However, quantitative mixing state data are challenging to obtain using single particle mass spectrometers. In this study, the quantitative chemical composition of carbonaceous single particles has been estimated using an aerosol time-of-flight mass spectrometer (ATOFMS) as part of the MEGAPOLI 2010 winter campaign in Paris, France. Relative peak areas of marker ions for elemental carbon (EC), organic aerosol (OA), ammonium, nitrate, sulphate and potassium were compared with concurrent measurements from an Aerodyne high resolution time-of-flight aerosol mass spectrometer (HR-ToF-AMS), a thermal/optical OCEC analyser and a particle into liquid sampler coupled with ion chromatography (PILS-IC). ATOFMS-derived mass concentrations reproduced the variability of these species well (R2 = 0.67-0.78), and ten discrete mixing states for carbonaceous particles were identified and quantified. Potassium content was used to identify particles associated with biomass combustion. The chemical mixing state of HR-ToF-AMS organic aerosol factors, resolved using positive matrix factorization, was also investigated through comparison with the ATOFMS dataset. The results indicate that hydrocarbon-like OA (HOA) detected in Paris is associated with two EC-rich mixing states which differ in their relative sulphate content, while fresh biomass burning OA (BBOA) is associated with two mixing states which differ significantly in their OA/EC ratios. Aged biomass burning OA (OOA2-BBOA) was found to be significantly internally mixed with nitrate, while secondary, oxidized OA (OOA) was associated with five particle mixing states, each exhibiting different relative secondary inorganic ion content. Externally mixed secondary organic aerosol was not observed. These findings demonstrate the heterogeneity of primary and

  7. Quantitative determination of carbonaceous particle mixing state in Paris using single particle mass spectrometer and aerosol mass spectrometer measurements

    Directory of Open Access Journals (Sweden)

    R. M. Healy

    2013-04-01

    Full Text Available Single particle mixing state information can be a powerful tool for assessing the relative impact of local and regional sources of ambient particulate matter in urban environments. However, quantitative mixing state data are challenging to obtain using single particle mass spectrometers. In this study, the quantitative chemical composition of carbonaceous single particles has been estimated using an aerosol time-of-flight mass spectrometer (ATOFMS as part of the MEGAPOLI 2010 winter campaign in Paris, France. Relative peak areas of marker ions for elemental carbon (EC, organic aerosol (OA, ammonium, nitrate, sulphate and potassium were compared with concurrent measurements from an Aerodyne high resolution time-of-flight aerosol mass spectrometer (HR-ToF-AMS, a thermal/optical OCEC analyser and a particle into liquid sampler coupled with ion chromatography (PILS-IC. ATOFMS-derived mass concentrations reproduced the variability of these species well (R2 = 0.67–0.78, and ten discrete mixing states for carbonaceous particles were identified and quantified. Potassium content was used to identify particles associated with biomass combustion. The chemical mixing state of HR-ToF-AMS organic aerosol factors, resolved using positive matrix factorization, was also investigated through comparison with the ATOFMS dataset. The results indicate that hydrocarbon-like OA (HOA detected in Paris is associated with two EC-rich mixing states which differ in their relative sulphate content, while fresh biomass burning OA (BBOA is associated with two mixing states which differ significantly in their OA/EC ratios. Aged biomass burning OA (OOA2-BBOA was found to be significantly internally mixed with nitrate, while secondary, oxidized OA (OOA was associated with five particle mixing states, each exhibiting different relative secondary inorganic ion content. Externally mixed secondary organic aerosol was not observed. These findings demonstrate the heterogeneity of

  8. Quantitative determination of carbonaceous particle mixing state in Paris using single-particle mass spectrometer and aerosol mass spectrometer measurements

    Directory of Open Access Journals (Sweden)

    R. M. Healy

    2013-09-01

    Full Text Available Single-particle mixing state information can be a powerful tool for assessing the relative impact of local and regional sources of ambient particulate matter in urban environments. However, quantitative mixing state data are challenging to obtain using single-particle mass spectrometers. In this study, the quantitative chemical composition of carbonaceous single particles has been determined using an aerosol time-of-flight mass spectrometer (ATOFMS as part of the MEGAPOLI 2010 winter campaign in Paris, France. Relative peak areas of marker ions for elemental carbon (EC, organic aerosol (OA, ammonium, nitrate, sulfate and potassium were compared with concurrent measurements from an Aerodyne high-resolution time-of-flight aerosol mass spectrometer (HR-ToF-AMS, a thermal–optical OCEC analyser and a particle into liquid sampler coupled with ion chromatography (PILS-IC. ATOFMS-derived estimated mass concentrations reproduced the variability of these species well (R2 = 0.67–0.78, and 10 discrete mixing states for carbonaceous particles were identified and quantified. The chemical mixing state of HR-ToF-AMS organic aerosol factors, resolved using positive matrix factorisation, was also investigated through comparison with the ATOFMS dataset. The results indicate that hydrocarbon-like OA (HOA detected in Paris is associated with two EC-rich mixing states which differ in their relative sulfate content, while fresh biomass burning OA (BBOA is associated with two mixing states which differ significantly in their OA / EC ratios. Aged biomass burning OA (OOA2-BBOA was found to be significantly internally mixed with nitrate, while secondary, oxidised OA (OOA was associated with five particle mixing states, each exhibiting different relative secondary inorganic ion content. Externally mixed secondary organic aerosol was not observed. These findings demonstrate the range of primary and secondary organic aerosol mixing states in Paris. Examination of the

  9. Quantitative determination of carbonaceous particle mixing state in Paris using single-particle mass spectrometer and aerosol mass spectrometer measurements

    Science.gov (United States)

    Healy, R. M.; Sciare, J.; Poulain, L.; Crippa, M.; Wiedensohler, A.; Prévôt, A. S. H.; Baltensperger, U.; Sarda-Estève, R.; McGuire, M. L.; Jeong, C.-H.; McGillicuddy, E.; O'Connor, I. P.; Sodeau, J. R.; Evans, G. J.; Wenger, J. C.

    2013-09-01

    Single-particle mixing state information can be a powerful tool for assessing the relative impact of local and regional sources of ambient particulate matter in urban environments. However, quantitative mixing state data are challenging to obtain using single-particle mass spectrometers. In this study, the quantitative chemical composition of carbonaceous single particles has been determined using an aerosol time-of-flight mass spectrometer (ATOFMS) as part of the MEGAPOLI 2010 winter campaign in Paris, France. Relative peak areas of marker ions for elemental carbon (EC), organic aerosol (OA), ammonium, nitrate, sulfate and potassium were compared with concurrent measurements from an Aerodyne high-resolution time-of-flight aerosol mass spectrometer (HR-ToF-AMS), a thermal-optical OCEC analyser and a particle into liquid sampler coupled with ion chromatography (PILS-IC). ATOFMS-derived estimated mass concentrations reproduced the variability of these species well (R2 = 0.67-0.78), and 10 discrete mixing states for carbonaceous particles were identified and quantified. The chemical mixing state of HR-ToF-AMS organic aerosol factors, resolved using positive matrix factorisation, was also investigated through comparison with the ATOFMS dataset. The results indicate that hydrocarbon-like OA (HOA) detected in Paris is associated with two EC-rich mixing states which differ in their relative sulfate content, while fresh biomass burning OA (BBOA) is associated with two mixing states which differ significantly in their OA / EC ratios. Aged biomass burning OA (OOA2-BBOA) was found to be significantly internally mixed with nitrate, while secondary, oxidised OA (OOA) was associated with five particle mixing states, each exhibiting different relative secondary inorganic ion content. Externally mixed secondary organic aerosol was not observed. These findings demonstrate the range of primary and secondary organic aerosol mixing states in Paris. Examination of the temporal

  10. Program GICC, final report (March 2005), inventory of carbonaceous aerosol particles from 1860 to 2100 or which carbonaceous aerosol for a significant climatic regional/global impact?

    International Nuclear Information System (INIS)

    The aim of our program is to determine past, present and future emission inventories of carbonaceous particles from 1860 to 2100 for fossil fuel and biofuel sources. Emission inventories for savannah and forest fires have been developed by using burnt area products given by satellite for Asia and Africa. The strong collaboration with the different groups attending this GICC program has allowed to develop the following results. 1- With the improvement of algorithms and new choices for emission factors, emission inventories for black carbon (BC), primary organic carbon (OCp) and total organic carbon (OCtot) have been constructed for the period 1950 to 1997 for fossil fuel and biofuel sources. With these new development, biofuel sources have been seen to be significant, especially in the developing countries. 2- Past inventories have been developed for fossil fuel and biofuel sources from 1860 to 1997 by taking into account the evolution of fuel consumption, fuel use and emission factors. 3- Savannah and forest fire inventories have been constructed based on burnt area products, for Africa (1981-1991, 2000) and Asia (2000-2001). These results show the importance of using real time data instead of statistics. 4-Future emission inventory of black carbon by fossil fuel sources has been constructed for 2100 following the IPCC scenario A2 (catastrophic case) and B1 (perfect world). 5-Characterization of biofuel emissions has been realized by organizing an experiment in a combustion chamber where indian and chinese biofuels (fuelwood, agricultural wastes, dung-cake etc..). were burnt, reproducing the burning methods used in these countries. 6-Finally, the differences between the existing inventories of carbonaceous aerosols has been explained. (A.L.B.)

  11. Characterization of trace metals in airborne carbonaceous aerosols by single-particle EDX – Scanning Electron Microscopy

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    Pietrodangelo A.

    2013-04-01

    Full Text Available The presence of fine and ultrafine metal particles has been evidenced in size segregated airborne carbonaceous aerosols collected at one industrial and two background (urban and rural sites during an extended field campaign in Central Italy. Analysis of the backscattered electrons (BSE by SEM – EDX demonstrated an effective potential in evidencing main structural features of the metal content in identified carbon aerosols. Many observed ultrafine metal particles appear embedded in the skeleton of carbonaceous individual particles and aggregates in the coarse fraction, while the same is not evident in the case of mixed carbon-sulphates aerosol that has been detected in the submicron size. These carbon-sulphates formations include indeed nano-sized metal particles that appear physically combined but not embedded. Also, larger metal particles (ranging around 1 μm physical size were observed close to carbon materials, but not included in their structure. Main compositional differences of metal particles with size segregation could be evidenced by energy – dispersive X ray spectrometry (EDX. Larger particles are mainly rich in Fe, frequently in presence of Mn, Cu, Cr and Zn in variable proportions; either oxidized or elemental metals were detected. On the other hand, ultrafine particles associated with carbon–sulphates aerosol are enriched in Pb and Zn, although the presence of other trace elements not detectable by SEM – EDX technique cannot be excluded. Moreover, Ce-enriched ultrafine particles were clearly determined in cenospheres. Conversely, inclusion of fine and ultrafine metal particles was rarely or not observed in soot aggregates.

  12. Global cloud condensation nuclei influenced by carbonaceous combustion aerosol

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    Spracklen, D. V.; Carslaw, K. S.; Pöschl, U.; Rap, A.; Forster, P. M.

    2011-09-01

    Black carbon in carbonaceous combustion aerosol warms the climate by absorbing solar radiation, meaning reductions in black carbon emissions are often perceived as an attractive global warming mitigation option. However, carbonaceous combustion aerosol can also act as cloud condensation nuclei (CCN) so they also cool the climate by increasing cloud albedo. The net radiative effect of carbonaceous combustion aerosol is uncertain because their contribution to CCN has not been evaluated on the global scale. By combining extensive observations of CCN concentrations with the GLOMAP global aerosol model, we find that the model is biased low (normalised mean bias = -77 %) unless carbonaceous combustion aerosol act as CCN. We show that carbonaceous combustion aerosol accounts for more than half (52-64 %) of global CCN with the range due to uncertainty in the emitted size distribution of carbonaceous combustion particles. The model predicts that wildfire and pollution (fossil fuel and biofuel) carbonaceous combustion aerosol causes a global mean cloud albedo aerosol indirect effect of -0.34 W m-2, with stronger cooling if we assume smaller particle emission size. We calculate that carbonaceous combustion aerosol from pollution sources cause a global mean aerosol indirect effect of -0.23 W m-2. The small size of carbonaceous combustion particles from fossil fuel sources means that whilst pollution sources account for only one-third of the emitted mass they cause two-thirds of the cloud albedo aerosol indirect effect that is due to carbonaceous combustion aerosol. This cooling effect must be accounted for, along with other cloud effects not studied here, to ensure that black carbon emissions controls that reduce the high number concentrations of fossil fuel particles have the desired net effect on climate.

  13. Microscopic Characterization of Carbonaceous Aerosol Particle Aging in the Outflow from Mexico City

    Energy Technology Data Exchange (ETDEWEB)

    Moffet, R. C.; Henn, T. R.; Tivanski, A. V.; Hopkins, R. J.; Desyaterik, Y.; Kilcoyne, A. L. D.; Tyliszczak, T.; Fast, J.; Barnard, J.; Shutthanandan, V.; Cliff, S.S.; Perry, K. D.; Laskin, A.; Gilles, M. K.

    2009-09-16

    This study was part of the Megacities Initiative: Local and Global Research Observations (MILAGRO) field campaign conducted in Mexico City Metropolitan Area during spring 2006. The physical and chemical transformations of particles aged in the outflow from Mexico City were investigated for the transport event of 22 March 2006. A detailed chemical analysis of individual particles was performed using a combination of complementary microscopy and micro-spectroscopy techniques. The applied techniques included scanning transmission X-ray microscopy (STXM) coupled with near edge X-ray absorption fine structure spectroscopy (NEXAFS) and computer controlled scanning electron microscopy with an energy dispersive X-ray analyzer (CCSEM/EDX). As the aerosol plume evolves from the city center, the organic mass per particle increases and the fraction of carbon-carbon double bonds (associated with elemental carbon) decreases. Organic functional groups enhanced with particle age include: carboxylic acids, alkyl groups, and oxygen bonded alkyl groups. At the city center (T0) the most prevalent aerosol type contained inorganic species (composed of sulfur, nitrogen, oxygen, and potassium) coated with organic material. At the T1 and T2 sites, located northeast of T0 (~;;29 km and ~;;65 km, respectively), the fraction of homogenously mixed organic particles increased in both size and number. These observations illustrate the evolution of the physical mixing state and organic bonding in individual particles in a photochemically active environment.

  14. Cloud albedo increase from carbonaceous aerosol

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    W. R. Leaitch

    2010-08-01

    Full Text Available Airborne measurements from two consecutive days, analysed with the aid of an aerosol-adiabatic cloud parcel model, are used to study the effect of carbonaceous aerosol particles on the reflectivity of sunlight by water clouds. The measurements, including aerosol chemistry, aerosol microphysics, cloud microphysics, cloud gust velocities and cloud light extinction, were made below, in and above stratocumulus over the northwest Atlantic Ocean. On the first day, the history of the below-cloud fine particle aerosol was marine and the fine particle sulphate and organic carbon mass concentrations measured at cloud base were 2.4 μg m−3 and 0.9 μg m−3 respectively. On the second day, the below-cloud aerosol was continentally influenced and the fine particle sulphate and organic carbon mass concentrations were 2.3 μg m−3 and 2.6 μg m−3 respectively. Over the range 0.06–0.8 μm diameter, the shapes of the below-cloud size distributions were similar on both days and the number concentrations were approximately a factor of two higher on the second day. The cloud droplet number concentrations (CDNC on the second day were approximately three times higher than the CDNC measured on the first day. Using the parcel model to separate the influence of the differences in gust velocities, we estimate from the vertically integrated cloud light scattering measurements a 6% increase in the cloud albedo principally due to the increase in the carbonaceous components on the second day. Assuming no additional absorption by this aerosol, a 6% albedo increase translates to a local daytime radiative cooling of ∼12 W m−2. This result provides observational evidence that the role of anthropogenic carbonaceous components in the cloud albedo effect can be much larger than that of anthropogenic sulphate, as some global simulations have indicated.

  15. Optical-chemical-microphysical relationships and closure studies for mixed carbonaceous aerosols observed at Jeju Island; 3-laser photoacoustic spectrometer, particle sizing, and filter analysis

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    B. A. Flowers

    2010-11-01

    Full Text Available Transport of aerosols in pollution plumes from the mainland Asian continent was observed in situ at Jeju, South Korea during the Cheju Asian Brown Cloud Plume-Asian Monsoon Experiment (CAPMEX field campaign throughout August and September 2008 using a 3-laser photoacoustic spectrometer (PASS-3, chemical filter analysis, and size distributions. The PASS-3 directly measures the effects of morphology (e.g. coatings on light absorption that traditional filter-based instruments are unable to address. Transport of mixed sulfate, carbonaceous, and nitrate aerosols from various Asian pollution plumes to Jeju accounted for 74% of the deployment days, showing large variations in their measured chemical and optical properties. Analysis of eight distinct episodes, spanning wide ranges of chemical composition, optical properties, and source regions, reveals that episodes with higher organic carbon (OC/sulfate (SO42− and nitrate (NO3/SO42− composition ratios exhibit lower single scatter albedo at shorter wavelengths (ω405. We infer complex refractive indices (n–ik as a function of wavelength for the high, intermediate, and low OC/SO42− pollution episodes by using the observed particle size distributions and the measured optical properties. The smallest mean particle diameter corresponds to the high OC/SO42− aerosol episode. The imaginary part of the refractive index (k is greater for the high OC/SO42− episode at all wavelengths. A distinct, sharp increase in k at short wavelength implies enhanced light absorption by OC, which accounts for 50% of the light absorption at 405 nm, in the high OC/SO42− episode. Idealized analysis indicates increased absorption at 781 nm by factors greater than 3 relative to denuded black carbon in the laboratory. We hypothesize

  16. [Investigation of Carbonaceous Airborne Particles by Scanning Proton Microprobe].

    Science.gov (United States)

    Bao, Liang-man; Liu, Jiang-feng; Lei, Qian-tao; Li, Xiao-lin; Zhang, Gui-lin; Li, Yan

    2016-01-15

    Carbonaceous particles are an important component of the atmospheric aerosol particles and important for global climate change, air quality and human health. The PM₁₀ single particles from two environmental monitor locations and seven pollution emission sources were analyzed using scanning proton microprobe (SPM) techniques. The concentration of carbon in individual particles was quantitatively determined by proton non-Rutherford elastic backscattering spectrometry (EBS). The results of this investigation showed that carbonaceous particles were dominant in the pollution sources of coal and oil combustions, diesel busexhaust and automobile exhaust, while inorganic particles were dominant in the sources of steel industry, cement dust and soil dust. Carbonaceous matter was enriched in particles from the city center, while mineral matter was the main component of airborne particles in the industrial area. Elemental mapping of single aerosol particles yielded important information on the chemical reactions of aerosol particles. The micro-PIXE (particle induced X-ray emission) maps of S, Ca and Fe of individual carbonaceous particles showed that sulfuration reaction occurred between SO₂and mineral particles, which increased the sulfur content of particles. PMID:27078933

  17. Carbonaceous aerosols from prescribed burning of a boreal forest ecosystem

    Energy Technology Data Exchange (ETDEWEB)

    Mazurek, M.A. (Brookhaven National Lab., Upton, NY (United States)); Cofer, W.R. III; Levine, J.S. (National Aeronautics and Space Administration, Hampton, VA (United States). Langley Research Center)

    1990-10-01

    The identity and ambient mass concentrations of radiatively important carbonaceous aerosols were measured for a boreal forest prescribed burn conducted in northern Ontario, CAN in August 1989. Nonsize-segregated airborne particles were collected for smoldering-fire and full-fire conditions using a helicopter sampling platform. Total carbon (TC), organic carbon (OC) and elemental carbon (EC) were measured. Smoke plume mass concentrations of the OC and EC particles were greatest for full-fire conditions and had ranges of 1.560 to 2.160 mg/m{sup {minus}1} (OC) and 0.120 to 0.160 mg/m{sup {minus}3} (EC) with OC:EC ratios of 10 to 18, respectively. Smoldering fire conditions showed smoke plume OC and EC levels of 0.570--1.030 mg/m{sup {minus}3} (OC) and 0.006--0.050 mg/m{sup {minus}3} (EC) and much higher ratios of OC:EC (21 to 95). These aerosol data indicate the formation of EC particles is greatest during full-fire combustion of boreal forest material relative to smoldering combustion. However, EC particles comprise a minor fraction of the particulate carbon smoke aerosols for both full-fire and smoldering conditions; the major component of carbonaceous smoke aerosols emitted during the prescribed burn is OC. Overall, the OC and EC in-plume smoke aerosol data show nonuniform production of these particles during various stages of the prescribed burn, and major differences in the type of carbonaceous aerosol that is generated (OC versus EC).

  18. Carbonaceous aerosols from prescribed burning of a boreal forest ecosystem

    International Nuclear Information System (INIS)

    The identity and ambient mass concentrations of radiatively important carbonaceous aerosols were measured for a boreal forest prescribed burn conducted in northern Ontario, CAN in August 1989. Nonsize-segregated airborne particles were collected for smoldering-fire and full-fire conditions using a helicopter sampling platform. Total carbon (TC), organic carbon (OC) and elemental carbon (EC) were measured. Smoke plume mass concentrations of the OC and EC particles were greatest for full-fire conditions and had ranges of 1.560 to 2.160 mg/m-1 (OC) and 0.120 to 0.160 mg/m-3 (EC) with OC:EC ratios of 10 to 18, respectively. Smoldering fire conditions showed smoke plume OC and EC levels of 0.570--1.030 mg/m-3 (OC) and 0.006--0.050 mg/m-3 (EC) and much higher ratios of OC:EC (21 to 95). These aerosol data indicate the formation of EC particles is greatest during full-fire combustion of boreal forest material relative to smoldering combustion. However, EC particles comprise a minor fraction of the particulate carbon smoke aerosols for both full-fire and smoldering conditions; the major component of carbonaceous smoke aerosols emitted during the prescribed burn is OC. Overall, the OC and EC in-plume smoke aerosol data show nonuniform production of these particles during various stages of the prescribed burn, and major differences in the type of carbonaceous aerosol that is generated (OC versus EC)

  19. Sources of carbonaceous aerosol in the Amazon basin

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    S. Gilardoni

    2011-03-01

    Full Text Available The quantification of sources of carbonaceous aerosol is important to understand their atmospheric concentrations and regulating processes and to study possible effects on climate and air quality, in addition to develop mitigation strategies.

    In the framework of the European Integrated Project on Aerosol Cloud Climate Interactions (EUCAARI fine (Dp < 2.5 μm and coarse (2.5 μm < Dp <10 μm aerosol particles were sampled from February to June (wet season and from August to September (dry season 2008 in the central Amazon basin. The mass of fine particles averaged 2.4 μg m−3 during the wet season and 4.2 μg m−3 during the dry season. The average coarse aerosol mass concentration during wet and dry periods was 7.9 and 7.6 μg m−3, respectively. The overall chemical composition of fine and coarse mass did not show any seasonality with the largest fraction of fine and coarse aerosol mass explained by organic carbon (OC; the average OC to mass ratio was 0.4 and 0.6 in fine and coarse aerosol modes, respectively. The mass absorbing cross section of soot was determined by comparison of elemental carbon and light absorption coefficient measurements and it was equal to 4.7 m2 g−1 at 637 nm. Carbon aerosol sources were identified by Positive Matrix Factorization (PMF analysis of thermograms: 44% of fine total carbon mass was assigned to biomass burning, 43% to secondary organic aerosol (SOA, and 13% to volatile species that are difficult to apportion. In the coarse mode, primary biogenic aerosol particles (PBAP dominated the carbonaceous aerosol mass. The results confirmed the importance of PBAP in forested areas.

    The source apportionment results were employed to evaluate the ability of global chemistry transport models to simulate carbonaceous aerosol sources in a regional tropical background site. The comparison showed an overestimation

  20. Monitoring of inorganic ions, carbonaceous matter and mass in ambient aerosol particles with online and offline methods

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    H. Timonen

    2011-10-01

    Full Text Available Year-long high timeresolution measurements of major chemical components in atmospheric sub-micrometer particles were conducted at an urban background station in Finland 2006–2007. Ions were analyzed using a particle-into-liquid sampler combined with an ion chromatograph (PILS-IC, organic and elemental carbon (OC and EC by using a semicontinuos OC/EC aerosol carbon analyzer (RT-OCEC, and PM2.5 mass with a tapered element oscillating microbalance (TEOM. Long time series provides information on differences between the used measurement techniques as well as information about the diurnal and seasonal changes. Chemical mass closure was constructed by comparing the identified aerosol mass with the measured PM2.5. The sum of all components measured online (ions, particulate organic matter (POM, EC represented only 65% of the total PM2.5 mass. The difference can be explained by the difference in cutoff sizes (PM1 for online measurements, PM2.5 for total mass and by evaporation of the semivolatile/volatile components. In general, some differences in results were observed when the results of the continuous/semicontinuous instruments were compared with those of the conventional filter samplings. For non-volatile compounds, like sulfate and potassium, correlation between the filter samples and the PILS was good but greater differences were observed for the semivolatile compounds like nitrate and ammonium. For OC the results of the RT-OCEC were on average 10% larger than those of the filters. When compared to filter measurements, high resolution measurements provide important data on short pollution plumes as well as on diurnal changes. Clear seasonal and diurnal cycles were observed for nitrate and EC.

  1. Monitoring of inorganic ions, carbonaceous matter and mass in ambient aerosol particles with online and offline methods

    Science.gov (United States)

    Timonen, H.; Aurela, M.; Saarnio, K.; Frey, A.; Saarikoski, S.; Teinilä, K.; Kulmala, M.; Hillamo, R.

    2011-10-01

    Year-long high timeresolution measurements of major chemical components in atmospheric sub-micrometer particles were conducted at an urban background station in Finland 2006-2007. Ions were analyzed using a particle-into-liquid sampler combined with an ion chromatograph (PILS-IC), organic and elemental carbon (OC and EC) by using a semicontinuos OC/EC aerosol carbon analyzer (RT-OCEC), and PM2.5 mass with a tapered element oscillating microbalance (TEOM). Long time series provides information on differences between the used measurement techniques as well as information about the diurnal and seasonal changes. Chemical mass closure was constructed by comparing the identified aerosol mass with the measured PM2.5. The sum of all components measured online (ions, particulate organic matter (POM), EC) represented only 65% of the total PM2.5 mass. The difference can be explained by the difference in cutoff sizes (PM1 for online measurements, PM2.5 for total mass) and by evaporation of the semivolatile/volatile components. In general, some differences in results were observed when the results of the continuous/semicontinuous instruments were compared with those of the conventional filter samplings. For non-volatile compounds, like sulfate and potassium, correlation between the filter samples and the PILS was good but greater differences were observed for the semivolatile compounds like nitrate and ammonium. For OC the results of the RT-OCEC were on average 10% larger than those of the filters. When compared to filter measurements, high resolution measurements provide important data on short pollution plumes as well as on diurnal changes. Clear seasonal and diurnal cycles were observed for nitrate and EC.

  2. Program GICC, final report (March 2005), inventory of carbonaceous aerosol particles from 1860 to 2100 or which carbonaceous aerosol for a significant climatic regional/global impact?; Programme GICC, RAPPORT DEFINITIF (Mars 2005), inventaire d'emissions d'aerosol carbone de 1860 a 2100 ou quelles emissions d'aerosol carbone pour un impact climatique regional/global significatif?

    Energy Technology Data Exchange (ETDEWEB)

    Cachier, H.; Guinot, B. [Laboratoire des Sciences du Climat et de l' Environnment, UMR CEA/CNRS 1572 - CEA Saclay, 91 - Gif sur Yvette (France); Criqui, P.; Mima, S. [IEPE, 38 - Grenoble (France); Brignon, J.M. [INERIS, 60 - Verneuil-en-Halatte (France); Penner, J. [Michigan Univ., Ann Arbor, MI (United States); Carmichael, G. [Iowa Univ., Iowa City, IA (United States); Gadi, R. [National Physical Lab., New Delhi (India); Denier Van der Gon, H. [TNO Hollande (Netherlands); Gregoire, J.M. [JRC, Ispra (Italy); Liousse, C.; Michel, C.; Guillaume, B.; Junker, C

    2007-07-01

    The aim of our program is to determine past, present and future emission inventories of carbonaceous particles from 1860 to 2100 for fossil fuel and biofuel sources. Emission inventories for savannah and forest fires have been developed by using burnt area products given by satellite for Asia and Africa. The strong collaboration with the different groups attending this GICC program has allowed to develop the following results. 1- With the improvement of algorithms and new choices for emission factors, emission inventories for black carbon (BC), primary organic carbon (OCp) and total organic carbon (OCtot) have been constructed for the period 1950 to 1997 for fossil fuel and biofuel sources. With these new development, biofuel sources have been seen to be significant, especially in the developing countries. 2- Past inventories have been developed for fossil fuel and biofuel sources from 1860 to 1997 by taking into account the evolution of fuel consumption, fuel use and emission factors. 3- Savannah and forest fire inventories have been constructed based on burnt area products, for Africa (1981-1991, 2000) and Asia (2000-2001). These results show the importance of using real time data instead of statistics. 4-Future emission inventory of black carbon by fossil fuel sources has been constructed for 2100 following the IPCC scenario A2 (catastrophic case) and B1 (perfect world). 5-Characterization of biofuel emissions has been realized by organizing an experiment in a combustion chamber where indian and chinese biofuels (fuelwood, agricultural wastes, dung-cake etc..). were burnt, reproducing the burning methods used in these countries. 6-Finally, the differences between the existing inventories of carbonaceous aerosols has been explained. (A.L.B.)

  3. Carbonaceous aerosols in an urban tunnel

    Science.gov (United States)

    Ancelet, Travis; Davy, Perry K.; Trompetter, William J.; Markwitz, Andreas; Weatherburn, David C.

    2011-08-01

    Particulate matter in the Mount Victoria Tunnel, an urban road tunnel 623 m in length with an average traffic volume of 2070-2300 vehicles per hour located in Wellington, New Zealand, was studied to gain an understanding of carbonaceous species emitted from motor vehicles. The average PM 2.5 concentration during peak hours in the tunnel was found to be 67.6 ± 19.4 μg m -3. Analysis of carbonaceous species present (OC, EC, TC) was performed by both the NIOSH and IMPROVE thermal/optical protocols and carbonaceous species were found to make up 63-73% of the total PM in the tunnel. Comparison of TC concentrations obtained from each protocol revealed that no significant difference was present between the two protocols. Black carbon (BC), also used as a measure of EC, was determined using light reflection and BC values did not differ significantly from EC concentrations determined using the NIOSH and IMPROVE protocols. TC was also determined using EA/IRMS and it was found that TC concentrations from EA/IRMS directly correlated with TC results obtained using the NIOSH protocol. Stable isotope analysis of the PM 2.5 yielded δ 13C values from -24.7 to -28.3‰, typical of motor vehicles. Analysis of particle-phase PAHs by thermal desorption GC/MS revealed an average total PAH concentration of 70.0 ± 4.1 ng m -3 and PAHs were found to contribute 0.10% of total PM 2.5 in the tunnel. PAH emissions in the tunnel were found to be enriched in low molecular weight PAHs, indicative of emissions from diesel-fueled vehicles. Analysis of individual particle composition and morphology revealed that most particles were carbonaceous species that formed large, amorphous agglomerates made up of smaller spherules.

  4. Carbonaceous aerosols from different tropical biomass burning sources

    Science.gov (United States)

    Cachier, Hélène; Brémond, Marie-Pierre; Buat-Ménard, Patrick

    1989-08-01

    FOLLOWING a repetitive pattern, biomass burning affects the intertropical belt on a continental scale during the dry season1. The importance of these anthropogenic activities with regard to carbonaceous-component emissions into the global atmosphere is now well recognized2-4. It has been suggested that large injections of black carbon aerosols from the Tropics are of potential importance for the radiative and chemical balance of the troposphere5-10. Studies on carbonaceous aerosols have indicated that, on an annual basis, the intensity of the emissions from tropical biomass burning could compare with that of emissions from fossil-fuel burning in industrial countries7,8. Also, results from combustion chamber experiments have determined the important range of the emission factor for both the organic and the black carbon components of the aerosol1-16. Following on from our earlier studies on total atmospheric particulate carbon (Ct) and isotopic composition (δ13C) (ref. 2), we now present new data on the black carbon content (Cb) of atmospheric particles sampled during the biomass-burning season in the wooden savannah of the Ivory Coast. The Cb/Ct ratio is generally lower than expected and highly variable. This variability indicates that there are drastic changes in source apportionment, which from our isotope studies may be ascribed to the variety of vegetation fuel and also to the mode of combustion. Therefore the Cb/Ct ratio can potentially discriminate biomass-burning emissions from different tropical ecosystems.

  5. Carbonaceous aerosols in Norwegian urban areas

    Directory of Open Access Journals (Sweden)

    K. E. Yttri

    2009-03-01

    Full Text Available Little is known regarding levels and source strength of carbonaceous aerosols in Scandinavia. In the present study, ambient aerosol (PM10 and PM2.5 concentrations of elemental carbon (EC, organic carbon (OC, water-insoluble organic carbon (WINSOC, and water-soluble organic carbon (WSOC are reported for a curbside site, an urban background site, and a suburban site in Norway in order to investigate their spatial and seasonal variations. Aerosol filter samples were collected using tandem filter sampling to correct for the positive sampling artefact introduced by volatile and semivolatile OC. Analyses were performed using the thermal optical transmission (TOT instrument from Sunset Lab Inc., which corrects for charring during analysis. Finally, we estimated the relative contribution of OC from wood burning based on the samples content of levoglucosan.

    Levels of EC varied by more than one order of magnitude between sites, likely due to the higher impact of vehicular traffic at the curbside and the urban background sites. In winter, the level of particulate organic carbon (OCp at the suburban site was equal to (for PM10 or even higher (for PM2.5 than the levels observed at the curbside and the urban background sites. This finding was attributed to the impact of residential wood burning at the suburban site in winter, which was confirmed by a high mean concentration of levoglucosan (407 ng m−3. This finding indicates that exposure to primary combustion derived OCp could be equally high in residential areas as in a city center. It is demonstrated that OCp from wood burning (OCwood accounted for almost all OCp at the suburban site in winter, allowing a new estimate of the ratio TCp/levoglucosan for both PM10 and PM2.5. Particulate carbonaceous material (PCM

  6. Spectro-microscopic measurements of carbonaceous aerosol aging in Central California

    Directory of Open Access Journals (Sweden)

    R. C. Moffet

    2013-04-01

    Full Text Available Carbonaceous aerosols are responsible for large uncertainties in climate models, degraded visibility, and adverse health effects. The Carbonaceous Aerosols and Radiative Effects Study (CARES was designed to study carbonaceous aerosols in the natural environment of Central Valley, California, and learn more about their atmospheric formation and aging. This paper presents results from spectro-microscopic measurements of carbonaceous particles collected during CARES at the time of pollution accumulation event (27–29 June 2010, when in situ measurements indicated an increase in the organic carbon content of aerosols as the Sacramento urban plume aged. Computer controlled scanning electron microscopy coupled with an energy dispersive X-ray detector (CCSEM/EDX and scanning transmission X-ray microscopy coupled with near edge X-ray absorption spectroscopy (STXM/NEXAFS were used to probe the chemical composition and morphology of individual particles. It was found that the mass of organic carbon on individual particles increased through condensation of secondary organic aerosol. STXM/NEXAFS indicated that the number fraction of homogenous organic particles lacking inorganic inclusions (greater than ~50 nm diameter increased with plume age as did the organic mass per particle. Comparison of the CARES spectro-microscopic data set with a similar dataset obtained in Mexico City during the MILAGRO campaign showed that individual particles in Mexico City contained twice as much carbon as those sampled during CARES. The number fraction of soot particles at the Mexico City urban site (30% was larger than at the CARES urban site (10% and the most aged samples from CARES contained less carbon-carbon double bonds. Differences between carbonaceous particles in Mexico City and California result from different sources, photochemical conditions, gas phase reactants, and secondary organic aerosol precursors. The detailed results provided by these spectro

  7. Characteristics and sources of carbonaceous aerosols from Shanghai, China

    Directory of Open Access Journals (Sweden)

    J.-J. Cao

    2013-01-01

    Full Text Available An intensive investigation of carbonaceous PM2.5 and TSP (total suspended particles from Pudong (China was conducted as part of the MIRAGE-Shanghai (Megacities Impact on Regional and Global Environment experiment in 2009. Data for organic and elemental carbon (OC and EC, organic species, including C17 to C40 n-alkanes and 17 polycyclic aromatic hydrocarbons (PAHs, and stable carbon isotopes OC (δ13COC and EC (δ13CEC were used to evaluate the aerosols' temporal variations and identify presumptive sources. High OC/EC ratios indicated a large fraction of secondary organic aerosol (SOA; high char/soot ratios indicated stronger contributions to EC from motor vehicles and coal combustion than biomass burning. Diagnostic ratios of PAHs indicated that much of the SOA was produced via coal combustion. Isotope abundances (δ13COC = −24.5 ± 0.8‰ and δ13CEC = −25.1 ± 0.6‰ indicated that fossil fuels were the most important source for carbonaceous PM2.5 (particulate matter less than 2.5 micrometers in diameter, with lesser impacts from biomass burning and natural sources. An EC tracer system and isotope mass balance calculations showed that the relative contributions to total carbon from coal combustion, motor vehicle exhaust, and SOA were 41%, 21%, and 31%; other primary sources such as marine, soil and biogenic emissions contributed 7%. Combined analyses of OC and EC, n-alkanes and PAHs, and stable carbon isotopes provide a new way to apportion the sources of carbonaceous particles.

  8. Characteristics and sources of carbonaceous aerosols from Shanghai, China

    Science.gov (United States)

    Cao, J.-J.; Zhu, C.-S.; Tie, X.-X.; Geng, F.-H.; Xu, H.-M.; Ho, S. S. H.; Wang, G.-H.; Han, Y.-M.; Ho, K.-F.

    2013-01-01

    An intensive investigation of carbonaceous PM2.5 and TSP (total suspended particles) from Pudong (China) was conducted as part of the MIRAGE-Shanghai (Megacities Impact on Regional and Global Environment) experiment in 2009. Data for organic and elemental carbon (OC and EC), organic species, including C17 to C40 n-alkanes and 17 polycyclic aromatic hydrocarbons (PAHs), and stable carbon isotopes OC (δ13COC) and EC (δ13CEC) were used to evaluate the aerosols' temporal variations and identify presumptive sources. High OC/EC ratios indicated a large fraction of secondary organic aerosol (SOA); high char/soot ratios indicated stronger contributions to EC from motor vehicles and coal combustion than biomass burning. Diagnostic ratios of PAHs indicated that much of the SOA was produced via coal combustion. Isotope abundances (δ13COC = -24.5 ± 0.8‰ and δ13CEC = -25.1 ± 0.6‰) indicated that fossil fuels were the most important source for carbonaceous PM2.5 (particulate matter less than 2.5 micrometers in diameter), with lesser impacts from biomass burning and natural sources. An EC tracer system and isotope mass balance calculations showed that the relative contributions to total carbon from coal combustion, motor vehicle exhaust, and SOA were 41%, 21%, and 31%; other primary sources such as marine, soil and biogenic emissions contributed 7%. Combined analyses of OC and EC, n-alkanes and PAHs, and stable carbon isotopes provide a new way to apportion the sources of carbonaceous particles.

  9. Characterization of carbonaceous aerosols in urban air

    Science.gov (United States)

    Husain, Liaquat; Dutkiewicz, Vincent A.; Khan, A. J.; Ghauri, Badar M.

    Concentrations of black carbon, [BC], were determined with an Aethalometer every 5 min at Lahore, a city of about 10 million in Pakistan, from 22 November 2005 to 31 January 2006. [BC] were very high, ranging from about 5 to 110μgm-3, with a mean of 21.7μgm-3. A distinct diurnal variation was observed: concentrations were lowest from about 10 a.m. to 4 p.m. local time (LT), and highest around 5-9 p.m. No clear relationship was observed between surface wind directions and [BC], although some of the highest concentrations were observed when the airflow was from southwest to northwest. The daily variations in concentrations were strongly affected by the diurnal variations in the mixing height; BC concentrations were low during the day when the mixing heights were high, ˜1000m, and very high at night when the mixing heights were low thermal-optical method. The [BC] were highly correlated with EC (r2=0.71), but on average 25% higher than [EC]. The [EC] and [OC] concentrations were moderately correlated (r2=0.65). The [OC]/[EC] ratios varied from 2.8 to 12, with a mean of 5.6. Although a large component of the carbonaceous aerosols in Lahore originated from fossil fuel combustion, a significant fraction was derived from biomass burning.

  10. Characteristics and sources of carbonaceous aerosols from Shanghai, China

    Directory of Open Access Journals (Sweden)

    J.-J. Cao

    2012-07-01

    Full Text Available An intensive investigation of carbonaceous PM2.5 and TSP from Pudong (China was conducted as part of the MIRAGE-Shanghai Experiment in 2009. Data for organic and elemental carbon (OC and EC, organic species, including C17 to C40 n-alkanes and 17 polycyclic aromatic hydrocarbons (PAHs, and stable C isotopes OC (δ13COC and EC (δ13CEC were used to evaluate the aerosols' temporal variations and identify presumptive sources. High OC/EC ratios indicated a large fraction of secondary organic aerosol (SOA; high char/soot ratios indicated stronger contributions to EC from motor vehicles and coal combustion than biomass burning. Diagnostic ratios of PAHs indicated that much of the SOA was produced via coal combustion. Isotope abundances (δ13COC = −24.5 ± 0.8‰ and δ13CEC = −25.1 ± 0.6‰ indicated that fossil fuels were the most important source for carbonaceous PM2.5, with lesser impacts from biomass burning and natural sources. An EC tracer system and isotope mass balance calculations showed that the relative contributions to total carbon from coal combustion, motor vehicle exhaust, and SOA were 41%, 21%, and 31%: other primary sources such as marine, soil and biogenic emissions contributed 7%. Combined analyses of OC and EC, n-alkanes and PAHs, and stable carbon isotopes provide a new way to apportion the sources of carbonaceous particles.

  11. Physical and Chemical Characterization of Carbonaceous Aerosols in Korea

    Science.gov (United States)

    Choung, S.; Jin, J. S.; Hwang, G. S.; Jang, K. S.; Han, W. S.; OH, J.; Kwon, Y.

    2014-12-01

    Atmospheric aerosols have been recently paid attention more in environmental research due to their negative effects on air quality, public health, and climate change. The aerosols contain approximately >20-50% carbonaceous components such as organic carbon (OC) and black carbon (BC) (or elemental carbon [EC]) derived from organic compounds, biomass burning, and incomplete combustion of fossil fuels. The physical, chemical, and biological properties of atmospheric aerosols are strongly dependent on the carbonaceous components. In particular, the BC could significantly affect the regional air quality in the northeastern Asia, because China is one of the foremost BC emission country in the world. Previous studies have mainly focused on the quantification and source identification for carbonaceous aerosols. However, understanding of physical and chemical properties for the carbonaceous aerosols related to environmental contamination and toxicity was still incomplete due to analytical difficulties. This study is addressed to evaluate the contribution of carbonaceous aerosols to air pollution through the surface, mass spectroscopic, and electron microscopic analyses, and determination of chemical composition and structure using the air particulate matter (PM2.5 and >PM2.5) samples.

  12. Emission factors of fine particles, carbonaceous aerosols and traces gases from road vehicles: Recent tests in an urban tunnel in the Pearl River Delta, China

    Science.gov (United States)

    Zhang, Yanli; Wang, Xinming; Li, Guanghui; Yang, Weiqiang; Huang, Zhonghui; Zhang, Zhou; Huang, Xinyu; Deng, Wei; Liu, Tengyu; Huang, Zuzhao; Zhang, Zhanyi

    2015-12-01

    Motor vehicles contribute primarily and secondarily to air quality problems due to fine particle (PM2.5) and ozone (O3) pollution in China's megacities. Characterizing vehicle emission with the rapid change of vehicle numbers and fleet compositions is vital for both bottom-up emission survey and top-down source apportioning. To obtain emission factors (EFs) of PM2.5, carbonaceous aerosols and trace gases for road vehicles, in urban Guangzhou we conducted a field campaign in 2014 in the Zhujiang Tunnel, a heavily burdened tunnel with about 40,000 motor vehicles passing through each of its two separated bores per day. PM2.5 and volatile organic compounds (VOCs) were sampled for offline analysis while trace gases including SO2, NOx and CO were measured online and in situ. An eddy covariance system with an integrated 3-D sonic anemometer was also adopted to measure CO2 and winds inside the tunnel. We recorded an average fleet composition of 61% light-duty gasoline vehicles (LDVs) + 12% heavy-duty diesel vehicles (HDVs) + 27% liquefied petroleum gas vehicles (LPGVs), and EFs of 82.7 ± 28.3, 19.3 ± 4.7 and 13.3 ± 3.3 mg veh-1 km-1, respectively, for PM2.5, organic carbon (OC) and elemental carbon (EC). These EFs were respectively 23.4%, 18.3% and 72.3% lower when compared to that measured in the same tunnel in 2004. EFs of PM2.5, OC and EC were higher at night time (148 ± 126, 29 ± 24 and 21 ± 18 mg veh-1 km-1, respectively) due to significantly elevated fractions of HDVs in the traffic fleets. An average ratio of OC to EC 1.45 from this tunnel study was much higher than that of ∼0.5 in previous tunnel studies. The EFs of SO2, NOx, CO, CO2 and NMHCs for road traffic were also obtained from our tunnel tests, and they were 20.7 ± 2.9, (1.29 ± 0.2)E+03, (3.10 ± 0.68)E+03, (3.90 ± 0.49)E+05, and 448 ± 39 mg veh-1 km-1, respectively.

  13. Measurements of non-volatile aerosols with a VTDMA and their correlations with carbonaceous aerosols in Guangzhou, China

    OpenAIRE

    Cheung, H. H. Y.; H. B. Tan; Xu, H. B.; F. Li; C. Wu; J. Z. Yu; Chan, C K

    2015-01-01

    Simultaneous measurements of aerosols of varying volatilities and carbonaceous matters at an urban site of Guangzhou, China were conducted in February and March 2014 using a Volatility Tandem Differential Mobility Analyzer (VTDMA) and an Organic Carbon/Elemental Carbon (OC/EC) Analyzer. In VTDMA, selected aerosols of 40 to 300 nm in mobility diameter were heated at elevated temperatures up to 300 °C and the size distributions of the residual particles were ...

  14. Climate implications of carbonaceous aerosols: An aerosol microphysical study using the GISS/MATRIX climate model

    Energy Technology Data Exchange (ETDEWEB)

    Bauer, Susanne E.; Menon, Surabi; Koch, Dorothy; Bond, Tami; Tsigaridis, Kostas

    2010-04-09

    Recently, attention has been drawn towards black carbon aerosols as a likely short-term climate warming mitigation candidate. However the global and regional impacts of the direct, cloud-indirect and semi-direct forcing effects are highly uncertain, due to the complex nature of aerosol evolution and its climate interactions. Black carbon is directly released as particle into the atmosphere, but then interacts with other gases and particles through condensation and coagulation processes leading to further aerosol growth, aging and internal mixing. A detailed aerosol microphysical scheme, MATRIX, embedded within the global GISS modelE includes the above processes that determine the lifecycle and climate impact of aerosols. This study presents a quantitative assessment of the impact of microphysical processes involving black carbon, such as emission size distributions and optical properties on aerosol cloud activation and radiative forcing. Our best estimate for net direct and indirect aerosol radiative forcing change is -0.56 W/m{sup 2} between 1750 and 2000. However, the direct and indirect aerosol effects are very sensitive to the black and organic carbon size distribution and consequential mixing state. The net radiative forcing change can vary between -0.32 to -0.75 W/m{sup 2} depending on these carbonaceous particle properties. Assuming that sulfates, nitrates and secondary organics form a coating shell around a black carbon core, rather than forming a uniformly mixed particles, changes the overall net radiative forcing from a negative to a positive number. Black carbon mitigation scenarios showed generally a benefit when mainly black carbon sources such as diesel emissions are reduced, reducing organic and black carbon sources such as bio-fuels, does not lead to reduced warming.

  15. Morphology, composition and mixing state of individual carbonaceous aerosol in urban Shanghai

    Directory of Open Access Journals (Sweden)

    H. Fu

    2011-07-01

    Full Text Available 834 individual aerosol particles were collected during Octoberober and Novemberember 2010 in urban Shanghai, China. Morphologies, compositions and mixing states of carbonaceous aerosols were investigated by transmission electron microscopy (TEM coupled with energy-dispersive X-ray (EDX. Structures of some particles were verified using selected-area electron diffraction (SAED. Among the aerosol particles observed, carbonaceous aerosols were categorized into five types: polymeric organic compound (POC, soot, tar ball, char, and biogenic particle. Based on the detailed TEM-EDX analysis, most of particles were coated with secondary organic aerosols (SOA, which commonly formed through condensation or heterogeneous reactions of precursor gases on pre-existing particles. The internally particles of sulphates, organics and soot were encountered frequently. Such internally mixed particles may be preferentially formed during a stagnated air mass which often occurred during serious pollution events, such as a haze episode on 13 Novemberember. Although relative number counts varied with different species, sulphates (38 %–71 % and soot (11 %–22 % constituted the most dominant species observed in the samples. With an exception of the sample collected during a dust storm on 12 Novemberember, soil-derived particles (68 % were relatively more frequently observed. Of particular interest was the biogenic particles encountered almost as frequently as soot on the sample collected on 13 November (18 % vs. 22 %. The result from air mass back-trajectory analysis indicated that these particles were marine-originated, most likely from the Yellow Sea.

  16. Changes in the vertical temperature structure associated with carbonaceous aerosols

    Energy Technology Data Exchange (ETDEWEB)

    Zhang, Y; Penner, J E; Chuang, C C; Santer, B D; Taylor, K

    2002-02-08

    Carbonaceous aerosols from anthropogenic activities act to both scatter and absorb solar radiation. It has been postulated that absorption by aerosols might significantly alter both the vertical temperature structure of the atmosphere and cloud fraction [Hansen et al. 1997, Ackerman et al, 2000]. Since both effects may alter the assessment of climate change associated with human activities, it is very important to understand both the magnitude and the mechanism by which carbonaceous aerosols affect climate. In this paper, we used a coupled climate and chemistry transport model to estimate the effects of carbonaceous aerosols on the vertical temperature structure and their effects on cloud fraction. A series Of control simulations were also carried out to compare the results of the model in which carbonaceous aerosols interact with climate with those in which they do not. We will present the temperature difference between simulations that include the effect of black carbon on the radiation field and those that do not, both at the surface and in the free troposphere. We will also discuss the change of temperature lapse rate and changes of cloud fraction associated with black carbon.

  17. Combustion generated fine carbonaceous particles

    OpenAIRE

    Bockhorn, Henning; D'Anna, Andrea; Sarofim, Adel F.; Wang, Hai

    2009-01-01

    Soot is of importance for its contribution to atmospheric particles with their adverse health impacts and for its contributions to heat transfer in furnaces and combustors, to luminosity from candles, and to smoke that hinders escape from buildings during fires and that impacts global warming or cooling. The different chapters of the book adress comprehensively the different aspects from fundamental approaches to applications in technical combustion devices.

  18. Spectro-microscopic measurements of carbonaceous aerosol aging in Central California

    Directory of Open Access Journals (Sweden)

    R. C. Moffet

    2013-10-01

    Full Text Available Carbonaceous aerosols are responsible for large uncertainties in climate models, degraded visibility, and adverse health effects. The Carbonaceous Aerosols and Radiative Effects Study (CARES was designed to study carbonaceous aerosols in the natural environment of the Central Valley, California, and learn more about their atmospheric formation and aging. This paper presents results from spectro-microscopic measurements of carbonaceous particles collected during CARES at the time of a pollution accumulation event (27–29 June 2010, when in situ measurements indicated an increase in the organic carbon content of aerosols as the Sacramento urban plume aged. Computer-controlled scanning electron microscopy coupled with an energy dispersive X-ray detector (CCSEM/EDX and scanning transmission X-ray microscopy coupled with near-edge X-ray absorption spectroscopy (STXM/NEXAFS were used to probe the chemical composition and morphology of individual particles. It was found that the mass of organic carbon on individual particles increased through condensation of secondary organic aerosol. STXM/NEXAFS indicated that the number fraction of homogenous organic particles lacking inorganic inclusions (greater than ~50 nm equivalent circular diameter increased with plume age, as did the organic mass per particle. Comparison of the CARES spectro-microscopic dataset with a similar dataset obtained in Mexico City during the MILAGRO campaign showed that fresh particles in Mexico City contained three times as much carbon as those sampled during CARES. The number fraction of soot particles at the Mexico City urban site (ranging from 16.6 to 47.3% was larger than at the CARES urban site (13.4–15.7%, and the most aged samples from CARES contained fewer carbon–carbon double bonds. Differences between carbonaceous particles in Mexico City and California result from different sources, photochemical conditions, gas phase reactants, and secondary organic aerosol

  19. Characterization of carbonaceous particles from lake sediments

    International Nuclear Information System (INIS)

    Spheroidal carbonaceous particles produced by high temperature combustion of coal and oil were found in high concentrations in lake sediments from areas of high acid deposition. The sediment record of these particles showing the onset of industrialisation correlates well with the record of acidification as indicated by diatom analysis. To find sources of the atmospheric deposition affecting a lake and its catchment, characterisation of the carbonaceous particles is necessary. A reference data set of particle chemistries from coal and oil power stations was produced using EDS generated data of 17 elements. Using multivariate statistical techniques, the most important elements for the coal/oil separation were identified and incorporated into a linear discriminant function which allocated fuel type with > 97% accuracy. Application of this technique to surface sediments in Scotland shows the influence of oil burning from outside the region. When applied to a full sediment core, the history of coal and oil combustion affecting the lake is seen and correlates well with known coal and oil consumption figures. Consequently this method could be used to add extra dating levels to sediment cores. The technique has been extended to include peat particles and could potentially be used on those from brown coal, lignite and oil shale combustion

  20. Carbonaceous aerosols from prescribed burning of a boreal forest ecosystem. Revision

    Energy Technology Data Exchange (ETDEWEB)

    Mazurek, M.A. [Brookhaven National Lab., Upton, NY (United States); Cofer, W.R. III; Levine, J.S. [National Aeronautics and Space Administration, Hampton, VA (United States). Langley Research Center

    1990-10-01

    The identity and ambient mass concentrations of radiatively important carbonaceous aerosols were measured for a boreal forest prescribed burn conducted in northern Ontario, CAN in August 1989. Nonsize-segregated airborne particles were collected for smoldering-fire and full-fire conditions using a helicopter sampling platform. Total carbon (TC), organic carbon (OC) and elemental carbon (EC) were measured. Smoke plume mass concentrations of the OC and EC particles were greatest for full-fire conditions and had ranges of 1.560 to 2.160 mg/m{sup {minus}1} (OC) and 0.120 to 0.160 mg/m{sup {minus}3} (EC) with OC:EC ratios of 10 to 18, respectively. Smoldering fire conditions showed smoke plume OC and EC levels of 0.570--1.030 mg/m{sup {minus}3} (OC) and 0.006--0.050 mg/m{sup {minus}3} (EC) and much higher ratios of OC:EC (21 to 95). These aerosol data indicate the formation of EC particles is greatest during full-fire combustion of boreal forest material relative to smoldering combustion. However, EC particles comprise a minor fraction of the particulate carbon smoke aerosols for both full-fire and smoldering conditions; the major component of carbonaceous smoke aerosols emitted during the prescribed burn is OC. Overall, the OC and EC in-plume smoke aerosol data show nonuniform production of these particles during various stages of the prescribed burn, and major differences in the type of carbonaceous aerosol that is generated (OC versus EC).

  1. Heterogeneous formation of HONO on carbonaceous aerosol

    Energy Technology Data Exchange (ETDEWEB)

    Ammann, M.; Kalberer, M.; Tabor, K. [Paul Scherrer Inst. (PSI), Villigen (Switzerland)] [and others

    1997-09-01

    Based on an on-line and in situ experimental approach, for the first time heterogeneous production of nitrous acid (HONO) on carbon aerosol at ambient pressure and low NO{sub 2} concentration has been quantified by use of a {sup 13}N tracer technique. (author) 1 fig., 4 refs.

  2. Natural Radionuclides and Isotopic Signatures for Determining Carbonaceous Aerosol Sources, Aerosol Lifetimes, and Washout Processes

    Energy Technology Data Exchange (ETDEWEB)

    Gaffney, Jeffrey [Univ. of Arkansas, Little Rock, AR (United States)

    2012-12-12

    This is the final technical report. The project description is as follows: to determine the role of aerosol radiative forcing on climate, the processes that control their atmospheric concentrations must be understood, and aerosol sources need to be determined for mitigation. Measurements of naturally occurring radionuclides and stable isotopic signatures allow the sources, removal and transport processes, as well as atmospheric lifetimes of fine carbonaceous aerosols, to be evaluated.

  3. Natural Radionuclides and Isotopic Signatures for Determining Carbonaceous Aerosol Sources, Aerosol Lifetimes, and Washout Processes

    International Nuclear Information System (INIS)

    This is the final technical report. The project description is as follows: to determine the role of aerosol radiative forcing on climate, the processes that control their atmospheric concentrations must be understood, and aerosol sources need to be determined for mitigation. Measurements of naturally occurring radionuclides and stable isotopic signatures allow the sources, removal and transport processes, as well as atmospheric lifetimes of fine carbonaceous aerosols, to be evaluated.

  4. Source apportionment of carbonaceous aerosol in southern Sweden

    Directory of Open Access Journals (Sweden)

    J. Genberg

    2011-05-01

    Full Text Available A one-year study was performed at the Vavihill background station in southern Sweden to estimate the anthropogenic contribution to the carbonaceous aerosol. Weekly samples of the particulate matter PM10 were collected on quartz filters, and the amounts of organic carbon, elemental carbon, radiocarbon (14C and levoglucosan were measured. This approach enabled source apportionment of the total carbon in the PM10 fraction using the concentration ratios of the sources. The sources considered in this study were emissions from the combustion of fossil fuels and biomass, as well as biogenic sources. During the summer, the carbonaceous aerosol mass was dominated by compounds of biogenic origin (82 %, which are associated with biogenic primary and secondary organic aerosols. During the winter months, biomass combustion (38 % and fossil fuel combustion (33 % were the main contributors to the carbonaceous aerosol. Elemental carbon concentrations in winter were about twice as large as during summer, and can be attributed to biomass combustion, probably from domestic wood burning. The contribution of fossil fuels to elemental carbon was stable throughout the year, although the fossil contribution to organic carbon increased during the winter. Thus, the organic aerosol originated mainly from natural sources during the summer and from anthropogenic sources during the winter. The result of this source apportionment was compared with results from the EMEP model. The model and measurements were generally consistent for total atmospheric organic carbon, however, the contribution of the sources varied substantially. E.g. the biomass burning contributions of OC were underestimated by the model by a factor of 8.2 compared to the measurements.

  5. Radiocarbon (14C) source apportionment of carbonaceous aerosol components in the Asian Atmospheric Brown Cloud

    International Nuclear Information System (INIS)

    Full text: Light-absorbing carbonaceous matter constitutes one of the largest uncertainties in climate modeling. The high concentrations of black carbon - soot - in the Asian Brown Cloud lead to strong atmospheric heating and large surface cooling that is as important to regional climate forcing as greenhouse gases, yet the sources of these aerosols are not well understood. Emission inventory models suggest that biofuel/biomass burning accounts for 60 - 90 % of the sources of these aerosol components whereas measurements of the elemental composition of ambient aerosols compared with source signatures point to combustion of fossil fuel as the primary culprit. However, both approaches acknowledge large uncertainties in source apportionment of the elusively defined black carbon. This study approached the sourcing challenge by applying microscale radiocarbon measurements to aerosol particles collected during the winter monsoon both over the Indian Ocean and in central India. The radiocarbon approach is ideally suited to this task as fossil sources are void of 14C whereas biomass combustion products hold a contemporary 14C signal. High-volume air samples of total carbonaceous aerosols revealed 14C signals that were similar for N. Indian source and Indian Ocean receptor regions, consistent with the absence of any significant formation of secondary organic aerosols, with a 60 - 70 % contribution from biomass combustion and biogenic sources. Isolates of elemental or soot carbon fractions varied between 40 - 70 %, depending on isolation method. These novel radiocarbon constraints on the sources of light-absorbing carbonaceous matter aid prioritizing of what combustion processes to target for emission mitigations of these health-afflicting and climate-forcing aerosols in the South Asian region. (author)

  6. Performance of a diffusion denuder for the elimination of sampling artifacts for carbonaceous aerosols at three urban and two forested sites in Europe

    Czech Academy of Sciences Publication Activity Database

    Maenhaut, W.; Chi, X.; Viana, M.; Mikuška, Pavel; Večeřa, Zbyněk

    Berkeley, 2008. s. 102. [International Conference on Carbonaceous Particles in the Atmosphere /9./. 12.08.2008-14.08.2008, Berkeley, California] Institutional research plan: CEZ:AV0Z40310501 Keywords : filter sampling artifacts * diffusion denuder * carbonaceous aerosol Subject RIV: CB - Analytical Chemistry, Separation

  7. Factors affecting the indoor concentrations of carbonaceous aerosols of outdoor origin

    Energy Technology Data Exchange (ETDEWEB)

    Lunden, Melissa M.; Kirchstetter, Thomas W.; Thatcher, Tracy L.; Hering, Susanne V.; Brown, Nancy J.

    2007-06-25

    A field study was conducted in an unoccupied single story residence in Clovis, California to provide data to address issues important to assess the indoor exposure to particles of outdoor origin. Measurements of black and organic carbonaceous aerosols were performed using a variety of methods, resulting in both near real-time measurements as well as integrated filter based measurements. Comparisons of the different measurement methods show that it is crucial to account for gas phase adsorption artifacts when measuring organic carbon (OC). Measured concentrations affected by the emissions of organic compounds sorbed to indoor surfaces imply a higher degree of infiltration of outdoor organic carbon aerosols into the indoor environment for our unoccupied house. Analysis of the indoor and outdoor data for black carbon (BC) aerosols show that, on average, the indoor concentration of black carbon aerosols behaves in a similar manner to sulfate aerosols. In contrast, organic carbon aerosols are subject to chemical transformations indoors that, for our unoccupied home, resulted in lower indoor OC concentrations than would be expected by physical loss mechanisms alone. These results show that gas to particle partitioning of organic compounds, as well as gas to surface interactions within the residence, are an important process governing the indoor concentration to OC aerosols of outdoor origin.

  8. Carbonaceous aerosol over semi-arid region of western India: Heterogeneity in sources and characteristics

    Science.gov (United States)

    Sudheer, A. K.; Aslam, M. Y.; Upadhyay, M.; Rengarajan, R.; Bhushan, R.; Rathore, J. S.; Singh, S. K.; Kumar, S.

    2016-09-01

    Carbonaceous species (elemental carbon (EC), organic carbon (OC), water-soluble organic carbon (WSOC)) and water-soluble inorganic species (Na+, NH4+, K+, Ca2 +, Mg2 +, Cl-, NO3-, SO42 -) in PM10 and PM2.5 from Ahmedabad and Jodhpur (urban and semi-urban locations, respectively) in western India were measured during May-September, 2011. Stable isotope composition of carbonaceous aerosol (δ13C of TC) in PM10 samples was also determined. Average EC concentration in PM10 at Ahmedabad was 1 μg m- 3 (range: 0.34 to 3.4 μg m- 3), almost 80% of which remained in PM2.5. Similarly, 70% of EC in PM10 (average: 0.9 μg m- 3) resided in PM2.5 at Jodhpur. Average OC concentration at Ahmedabad was 6.4 μg m- 3 and ~ 52% of this was found in PM2.5. On the contrary, OC concentration at Jodhpur was 40 μg m- 3, 80% of which was found in coarse particles contributing substantially to aerosol mass. δ13C of TC (average: - 27.5‰, range: - 29.6 to - 25.8‰) along with WSOC/EC ratio shows an increasing trend at Jodhpur suggesting the possibility of aging of aerosol, since aging results in enrichment of heavier isotope. OC and WSOC show significant correlations with K+ and not with EC, indicating biogenic origin of OC. Different size distributions are also exhibited by WSOC at the two stations. On the other hand, δ13C exhibits an inverse trend with sea-salt constituents at Ahmedabad, indicating the influence of air masses transported from the western/south-western region on carbonaceous aerosol. These results suggest that a strong heterogeneity exists in the sources of carbonaceous aerosol over this region and potential sources of non-combustion emissions such as bio-aerosol that need further investigation.

  9. Optical-chemical-microphysical relationships and closure studies for mixed carbonaceous aerosols observed at Jeju Island; 3-laser photoacoustic spectrometer, particle sizing, and filter analysis

    OpenAIRE

    B. A. Flowers; Dubey, M.K.; C. Mazzoleni; Stone, E. A.; J. J. Schauer; Kim, S. -W.; Yoon, S.C.

    2010-01-01

    Transport of aerosols in pollution plumes from the mainland Asian continent was observed in situ at Jeju, South Korea during the Cheju Asian Brown Cloud Plume-Asian Monsoon Experiment (CAPMEX) field campaign throughout August and September 2008 using a 3-laser photoacoustic spectrometer (PASS-3), chemical filter analysis, and size distributions. The PASS-3 directly measures the effects of morphology (e.g. coatings) on light absorption that traditional filter-based instruments are unable to ad...

  10. Impact of carbonaceous aerosol emissions on regional climate change

    Science.gov (United States)

    Roeckner, E.; Stier, P.; Feichter, J.; Kloster, S.; Esch, M.; Fischer-Bruns, I.

    2006-11-01

    The past and future evolution of atmospheric composition and climate has been simulated with a version of the Max Planck Institute Earth System Model (MPI-ESM). The system consists of the atmosphere, including a detailed representation of tropospheric aerosols, the land surface, and the ocean, including a model of the marine biogeochemistry which interacts with the atmosphere via the dust and sulfur cycles. In addition to the prescribed concentrations of carbon dioxide, ozone and other greenhouse gases, the model is driven by natural forcings (solar irradiance and volcanic aerosol), and by emissions of mineral dust, sea salt, sulfur, black carbon (BC) and particulate organic matter (POM). Transient climate simulations were performed for the twentieth century and extended into the twenty-first century, according to SRES scenario A1B, with two different assumptions on future emissions of carbonaceous aerosols (BC, POM). In the first experiment, BC and POM emissions decrease over Europe and China but increase at lower latitudes (central and South America, Africa, Middle East, India, Southeast Asia). In the second experiment, the BC and POM emissions are frozen at their levels of year 2000. According to these experiments the impact of projected changes in carbonaceaous aerosols on the global mean temperature is negligible, but significant changes are found at low latitudes. This includes a cooling of the surface, enhanced precipitation and runoff, and a wetter surface. These regional changes in surface climate are caused primarily by the atmospheric absorption of sunlight by increasing BC levels and, subsequently, by thermally driven circulations which favour the transport of moisture from the adjacent oceans. The vertical redistribution of solar energy is particularly large during the dry season in central Africa when the anomalous atmospheric heating of up to 60 W m-2 and a corresponding decrease in surface solar radiation leads to a marked surface cooling, reduced

  11. Source apportionment of the summer time carbonaceous aerosol at Nordic rural background sites

    Directory of Open Access Journals (Sweden)

    K. E. Yttri

    2011-12-01

    Full Text Available In the present study, natural and anthropogenic sources of particulate organic carbon (OCp and elemental carbon (EC have been quantified based on weekly filter samples of PM10 (particles with aerodynamic diameter <10 μm collected at four Nordic rural background sites [Birkenes (Norway, Hyytiälä (Finland, Vavihill (Sweden, Lille Valby, (Denmark] during late summer (5 August–2 September 2009. Levels of source specific tracers, i.e. cellulose, levoglucosan, mannitol and the 14C/12C ratio of total carbon (TC, have been used as input for source apportionment of the carbonaceous aerosol, whereas Latin Hypercube Sampling (LHS was used to statistically treat the multitude of possible combinations resulting from this approach. The carbonaceous aerosol (here: TCp; i.e. particulate TC was totally dominated by natural sources (69–86%, with biogenic secondary organic aerosol (BSOA being the single most important source (48–57%. Interestingly, primary biological aerosol particles (PBAP were the second most important source (20–32%. The anthropogenic contribution was mainly attributed to fossil fuel sources (OCff and ECff (10–24%, whereas no more than 3–7% was explained by combustion of biomass (OCbb and ECbb in this late summer campaign i.e. emissions from residential wood burning and/or wild/agricultural fires. Fossil fuel sources totally dominated the ambient EC loading, which accounted for 4–12% of TCp, whereas <1.5% of EC was attributed to combustion of biomass. The carbonaceous aerosol source apportionment showed only minor variation between the four selected sites. However, Hyytiälä and Birkenes showed greater resemblance to each other, as did Lille Valby and Vavihill, the two latter being somewhat more influenced by anthropogenic sources. Ambient levels of organosulphates and nitrooxy-organosulphates in the Nordic rural

  12. Spatial and seasonal variability of carbonaceous aerosol across Italy

    Science.gov (United States)

    Sandrini, Silvia; Fuzzi, Sandro; Piazzalunga, Andrea; Prati, Paolo; Bonasoni, Paolo; Cavalli, Fabrizia; Bove, Maria Chiara; Calvello, Mariarosaria; Cappelletti, David; Colombi, Cristina; Contini, Daniele; de Gennaro, Gianluigi; Di Gilio, Alessia; Fermo, Paola; Ferrero, Luca; Gianelle, Vorne; Giugliano, Michele; Ielpo, Pierina; Lonati, Giovanni; Marinoni, Angela; Massabò, Dario; Molteni, Ugo; Moroni, Beatrice; Pavese, Giulia; Perrino, Cinzia; Perrone, Maria Grazia; Perrone, Maria Rita; Putaud, Jean-Philippe; Sargolini, Tiziana; Vecchi, Roberta; Gilardoni, Stefania

    2014-12-01

    This paper analyses elemental (EC), organic (OC) and total carbon (TC) concentration in PM2.5 and PM10 samples collected over the last few years within several national and European projects at 37 remote, rural, urban, and traffic sites across the Italian peninsula. The purpose of the study is to obtain a picture of the spatial and seasonal variability of these aerosol species in Italy, and an insight into sources, processes and effects of meteorological conditions. OC and EC showed winter maxima and summer minima at urban and rural locations and an opposite behaviour at remote high altitude sites, where they increase during the warm period due to the rising of the Planetary Boundary Layer (PBL). The seasonal averages of OC are higher during winter compared to summer at the rural sites in the Po Valley (from 1.4 to 3.5 times), opposite to what usually occurs at rural locations, where OC increases during the warm period. This denotes the marked influence of urban areas on the surrounding rural environment in this densely populated region. The different types of sites exhibit marked differences in the average concentrations of carbonaceous aerosol and OC/EC ratio. This ratio is less sensitive to atmospheric processing than OC and EC concentrations, and hence more representative of different source types. Remote locations are characterised by the lowest levels of OC and especially EC, with OC/EC ratios ranging from 13 to 20, while the maximum OC and EC concentrations are observed at road-traffic influenced urban sites, where the OC/EC ratio ranges between 1 and 3. The highest urban impacts of OC and EC relative to remote and rural background sites occur in the Po Valley, especially in the city of Milan, which has the highest concentrations of PM and TC and low values of the OC/EC ratio.

  13. Source apportionment of the summer time carbonaceous aerosol at Nordic rural background sites

    Directory of Open Access Journals (Sweden)

    K. E. Yttri

    2011-06-01

    Full Text Available In the present study, natural and anthropogenic sources of particulate organic carbon (OCp and elemental carbon (EC have been quantified based on weekly filter samples of PM10 collected at four Nordic rural background sites (Birkenes (Norway, Hyytiälä (Finland Vavihill (Sweden, Lille Valby (Denmark during late summer (5 August–2 September 2009. Levels of source specific tracers, i.e. cellulose, levoglucosan, mannitol and the 14C/12C ratio of total carbon (TC, have been used as input for source apportionment of the carbonaceous aerosol, whereas Latin Hypercube Sampling (LHS was used to statistically treat the multitude of possible combinations resulting from this approach.

    The carbonaceous aerosol (here: TCp; i.e. particulate TC was totally dominated by natural sources (69–86 %, with biogenic secondary organic aerosol (BSOA being the single most important source (48–57 %. Interestingly, primary biological aerosol particles (PBAP were the second most important source (20–32 %. The anthropogenic contribution was mainly attributed to fossil fuel sources (OCff and ECff (10–24 %, whereas no more than 3–7 % was explained by combustion of biomass (OCbb and ECbb in this late summer campaign i.e. emissions from residential wood burning and/or wild/agricultural fires. Fossil fuel sources totally dominated the ambient EC loading, accounting for 4–12 % of TCp, whereas <1.5 % was attributed to combustion of biomass. The carbonaceous aerosol source apportionment showed only minor variation between the four selected sites. However, Hyytiälä and Birkenes showed greater resemblance to each other, as did Lille Valby and Vavihill, the two latter being somewhat more influenced by anthropogenic sources.

    Ambient levels of organosulphates and nitrooxy-organosulphates in the Nordic rural background environment are reported for

  14. Measurement of carbonaceous aerosol with different sampling configurations and frequencies

    Directory of Open Access Journals (Sweden)

    Y. Cheng

    2015-03-01

    Full Text Available Carbonaceous aerosol in Beijing, China was measured with different sampling configurations (denuded vs. un-denuded and frequencies (24 vs. 48 h averaged. Our results suggest that the negative sampling artifact of a bare quartz filter could be remarkably enhanced due to the uptake of water vapor by the filter medium, indicating that the positive sampling artifact tends to be underestimated under high humidity conditions. It was also observed that the analytical artifact (i.e., the underestimation of elemental carbon by the operationally defined value of the thermal-optical method was more apparent for the low frequency samples such that their elemental carbon (EC concentrations were about 15% lower than the reference values measured by the high-frequency, denuded filters. Moreover, EC results of the low frequency samples were found to exhibit a stronger dependence on the charring correction method. In addition, optical attenuation (ATN of EC was retrieved from the carbon analyzer, and the low frequency samples were shown to be more significantly biased by the shadowing effect.

  15. Measurements of non-volatile aerosols with a VTDMA and their correlations with carbonaceous aerosols in Guangzhou, China

    Directory of Open Access Journals (Sweden)

    H. H. Y. Cheung

    2015-09-01

    Full Text Available Simultaneous measurements of aerosols of varying volatilities and carbonaceous matters at an urban site of Guangzhou, China were conducted in February and March 2014 using a Volatility Tandem Differential Mobility Analyzer (VTDMA and an Organic Carbon/Elemental Carbon (OC/EC Analyzer. In VTDMA, selected aerosols of 40 to 300 nm in mobility diameter were heated at elevated temperatures up to 300 °C and the size distributions of the residual particles were measured. Size dependent distributions were observed for both non-volatile and volatile materials (VM. The 40 nm particles were dominated by particles that completely vaporized (CV at 300 °C, with an average number fraction of about 0.4. Particles larger than 80 nm were dominated by the medium and low volatility (MV and LV, respectively fractions, with average number fractions of 0.5 and 0.15 respectively. VM did not contribute separately to number fraction but contributed to over 50 % of the total volume fraction for all sizes. In both number and volume fractions, diurnal variation was only observed for the high volatility (HV group, CV and VM in 40 nm particles, likely because these particles were related to fresh emissions. The little diurnal variation of larger particles could be attributed to non-locally aged aerosols. Closure analysis between the residual mass of LV + MV and mass of EC or EC+OC2–4 (sum of EC, OC2, OC3, and OC4 of the OC/EC Analyzer suggests that non-volatile materials measured by the VTDMA likely contain less volatile OC.

  16. Measurements of non-volatile aerosols with a VTDMA and their correlations with carbonaceous aerosols in Guangzhou, China

    Science.gov (United States)

    Cheung, H. H. Y.; Tan, H. B.; Xu, H. B.; Li, F.; Wu, C.; Yu, J. Z.; Chan, C. K.

    2015-09-01

    Simultaneous measurements of aerosols of varying volatilities and carbonaceous matters at an urban site of Guangzhou, China were conducted in February and March 2014 using a Volatility Tandem Differential Mobility Analyzer (VTDMA) and an Organic Carbon/Elemental Carbon (OC/EC) Analyzer. In VTDMA, selected aerosols of 40 to 300 nm in mobility diameter were heated at elevated temperatures up to 300 °C and the size distributions of the residual particles were measured. Size dependent distributions were observed for both non-volatile and volatile materials (VM). The 40 nm particles were dominated by particles that completely vaporized (CV) at 300 °C, with an average number fraction of about 0.4. Particles larger than 80 nm were dominated by the medium and low volatility (MV and LV, respectively) fractions, with average number fractions of 0.5 and 0.15 respectively. VM did not contribute separately to number fraction but contributed to over 50 % of the total volume fraction for all sizes. In both number and volume fractions, diurnal variation was only observed for the high volatility (HV) group, CV and VM in 40 nm particles, likely because these particles were related to fresh emissions. The little diurnal variation of larger particles could be attributed to non-locally aged aerosols. Closure analysis between the residual mass of LV + MV and mass of EC or EC+OC2-4 (sum of EC, OC2, OC3, and OC4 of the OC/EC Analyzer) suggests that non-volatile materials measured by the VTDMA likely contain less volatile OC.

  17. Assessment of Artifacts in Filter Collections for Carbonaceous Aerosol and the Particulate Mass

    Czech Academy of Sciences Publication Activity Database

    Maenhaut, W.; Cafmeyer, J.; Chi, X.; Schwarz, Jaroslav

    2001, s. S673-S674. [European Aerosol Conference EAC 2001. Leipzig (DE), 03.09.2001-07.09.2001] Institutional research plan: CEZ:AV0Z4072921 Keywords : filter sampling * artifacts * carbonaceous aerosol Subject RIV: CF - Physical ; Theoretical Chemistry

  18. Patterns in atmospheric carbonaceous aerosols in China: emission estimates and observed concentrations

    Directory of Open Access Journals (Sweden)

    H. Cui

    2015-03-01

    rural and remote sites, attributed partly to weaker atmospheric oxidation and SOC formation compared to summer. Enhanced SOC formation from oxidization and anthropogenic activities like biomass combustion is judged to have crucial effects on severe haze events characterized by high particle concentrations. Several observational studies indicate an increasing trend in ambient OC/EC (but not in OC or EC individually from 2000 to 2010, confirming increased atmospheric oxidation of OC across the country. Combining the results of emission estimation and observations, the improvement over prior emission inventories is indicated by inter-annual comparisons and correlation analysis. It is also indicated, however, that the estimated growth in emissions might be faster than observed growth, and that some sources with high primary OC/EC like burning of biomass are still underestimated. Further studies to determine changing emission factors over time in the residential sector and to compare to other measurements such as satellite observations are thus suggested to improve understanding of the levels and trends of primary carbonaceous aerosol emissions in China.

  19. Sources and composition of urban aerosol particles

    Science.gov (United States)

    Vogt, M.; Johansson, C.; Mårtensson, M.; Struthers, H.; Ahlm, L.; Nilsson, D.

    2011-09-01

    From May 2008 to March 2009 aerosol emissions were measured using the eddy covariance method covering the size range 0.25 to 2.5 μm diameter (Dp) from a 105 m tower, in central Stockholm, Sweden. Supporting chemical aerosol data were collected at roof and street level. Results show that the inorganic fraction of sulfate, nitrate, ammonium and sea salt accounts for approximately 15% of the total aerosol mass water soluble soil contributing 11% and water insoluble soil 47%. Carbonaceous compounds were at the most 27% of PM1 mass. It was found that heating the air from the tower to 200 °C resulted in the loss of approximately 60% of the aerosol volume at 0.25 μm Dp whereas only 40% of the aerosol volume was removed at 0.6 μm Dp. Further heating to 300 °C caused very little additional losses roof level in the city, supporting the assumption that the non-volatile material consists of carbonaceous compounds. The average diurnal cycles of the BC emissions from road traffic (as inferred from the ratio of the incremental concentrations of nitrogen oxides (NOx) and BC measured on a densely trafficked street) and the fluxes of non-volatile material at tower level are in close agreement, suggesting a traffic source of BC. We have estimated the emission factors (EFs) for non-volatile particles <0.6 μm Dp to be 2.4±1.4 mg veh-1 km-1 based on either CO2 fluxes or traffic activity data. Light (LDV) and heavy duty vehicle (HDV) EFs were estimated using multiple linear regression and reveal that for non-volatile particulate matter in the 0.25 to 0.6 μm Dp range, the EFHDV is approximately twice as high as the EFLDV, the difference not being statistically significant.

  20. Significant influence of fungi on coarse carbonaceous and potassium aerosols in a tropical rainforest

    International Nuclear Information System (INIS)

    Fungal spores are ubiquitous in the Earth’s atmosphere, especially in the environment of tropical rainforests with intense biological activities. To assess the impact of fungi on chemical components of atmospheric aerosols at a Chinese tropical rainforest site, size-segregated fungal spore tracers (i.e. arabitol and mannitol) were measured along with major aerosol components, including carbonaceous species and water-soluble inorganic ions. The fungal spore tracers were found to be predominately associated with coarse particles, in which organic carbon (OC) and potassium (K+) were also present at significant levels. Enhanced amounts of fungal spore tracers were closely linked to rainfall events. Moreover, fungal spore tracers exhibited positive correlations with relative humidity and negative correlations with wind speed, temperature or radiation. The relationships between fungal spore tracers and meteorological factors are consistent with the emission features of actively discharged fungal spores, which are generally associated with sugar alcohols and by-products such as the inorganic ion K+. The excellent correlations between fungal spore tracers and OC or K+ in the coarse particles further suggested their common emission sources. Absolute principal factor analysis further identified fungi as the largest contributor to coarse OC and K+ (both at ∼66%) in this rainforest. (letter)

  1. Seasonal variation of urban carbonaceous aerosols in a typical city Nanjing in Yangtze River Delta, China

    Science.gov (United States)

    Li, Bing; Zhang, Jie; Zhao, Yu; Yuan, Siyu; Zhao, Qiuyue; Shen, Guofeng; Wu, Haisuo

    2015-04-01

    The Yangtze River Delta (YRD) is one of the regions with the most dynamic economy and severe atmospheric pollution in China. In order to characterize the particle features, especially the carbonaceous component in the YRD, particulate matter smaller than 2.5 μm (PM2.5) and 10 μm (PM10) samples in each season were collected in urban Nanjing, a typical city that locates in the west part of the YRD. The organic carbon (OC) and elemental carbon (EC) was differentiated using the thermal optical reflectance method. The average concentrations of PM2.5, OC and EC during the study periods were observed to be 117.6, 13.8, and 5.3 μg/m3 respectively, with all the highest levels in winter. The mass fraction of the Total carbonaceous aerosol (TCA) in PM2.5 was estimated at 23% on average, lower than those reported for other cities in the YRD. The OC and EC correlated well in all the seasons, especially in spring and winter, implying that OC and EC were attributed to common emission sources. Good correlation was observed between OC and estimated K+ from biomass burning in the harvest season in autumn and summer, indicating biomass burning a significant source of carbonaceous aerosols. This could also be confirmed by the lower fraction of OC3 + OC4 in OC during autumn and summer. The secondary organic carbon (SOC) estimated by EC-tracer method was the highest in winter (7.3 μg/m3) followed by autumn (6.7 μg/m3), summer (3.7 μg/m3) and spring (2.0 μg/m3). However, the SOC/OC in winter was not as high as that in summer and autumn, implying the high concentration of OC in winter was probably due to the stable weather but not mainly caused by SOC formation. The high SOC/OC ratio in summer was attributed to stronger oxidation, which could be suggested by higher sulfur oxidation ratio (SOR).

  2. Sulfur dioxide and primary carbonaceous aerosol emissions in China and India, 1996–2010

    OpenAIRE

    Lu, Z.; Q. Zhang; D. G. Streets

    2011-01-01

    China and India are the two largest anthropogenic aerosol generating countries in the world. In this study, we develop a new inventory of sulfur dioxide (SO2) and primary carbonaceous aerosol (i.e., black and organic carbon, BC and OC) emissions from these two countries for the period 1996–2010, using a technology-based methodology. Emissions from major anthropogenic sources and open biomass burning are included, and time-dependent trends in activity rates and emission ...

  3. Characteristics of Anthropogenic Sulfate and Carbonaceous Aerosols over East Asia: Regional Modeling and Observation

    Institute of Scientific and Technical Information of China (English)

    Yan HUANG; William L. CHAMEIDES; Qian TAN; Robert E. DICKINSON

    2008-01-01

    The authors present spatial and temporal characteristics of anthropogenic sulfate and carbonaceous aerosols over East Asia using a 3-D coupled regional climate-chemistry-aerosol model, and compare the simulation with the limited aerosol observations over the region. The aerosol module consists of SO2, SO42-, hydrophobic and hydrophilic black carbon (BC) and organic carbon compounds (OC), including emission, advections, dry and wet deposition, and chemical production and conversion. The simulated patterns of SO2 are closely tied to its emission rate, with sharp gradients between the highly polluted regions and more rural areas. Chemical conversion (especially in the aqueous phase) and dry deposition remove 60% and 30% of the total SO2 emission, respectively. The SO42- shows less horizontal gradient and seasonality than SO2, with wet deposition (60%) and export (27%) being two major sinks. Carbonaceous aerosols are spatially smoother than sulfur species. The aging process transforms more than 80% of hydrophobic BC and OC to hydrophilic components, which are removed by wet deposition (60%) and export (30%). The simulated spatial and seasonal SO42-, BC and OC aerosol concentrations and total aerosol optical depth are generally consistent with the observations in rural areas over East Asia, with lower bias in simulated OC aerosols, likely due to the underestimation of anthropogenic OC emissions and missing treatment of secondary organic carbon. The results suggest that our model is a useful tool for characterizing the anthropogenic aerosol cycle and for assessing its potential climatic and environmental effects in future studies.

  4. Atmospheric carbonaceous aerosols from Indo-Gangetic Plain and Central Himalaya: impact of anthropogenic sources.

    Science.gov (United States)

    Ram, Kirpa; Sarin, M M

    2015-01-15

    In the present-day scenario of growing anthropogenic activities, carbonaceous aerosols contribute significantly (∼20-70%) to the total atmospheric particulate matter mass and, thus, have immense potential to influence the Earth's radiation budget and climate on a regional to global scale. In addition, formation of secondary organic aerosols is being increasingly recognized as an important process in contributing to the air-pollution and poor visibility over urban regions. It is, thus, essential to study atmospheric concentrations of carbonaceous species (EC, OC and WSOC), their mixing state and absorption properties on a regional scale. This paper presents the comprehensive data on emission sources, chemical characteristics and optical properties of carbonaceous aerosols from selected urban sites in the Indo-Gangetic Plain (IGP) and from a high-altitude location in the central Himalaya. The mass concentrations of OC, EC and WSOC exhibit large spatio-temporal variability in the IGP. This is attributed to seasonally varying emissions from post-harvest agricultural-waste burning, their source strength, boundary layer dynamics and secondary aerosol formation. The high concentrations of OC and SO4(2-), and their characteristic high mass scattering efficiency, contribute significantly to the aerosol optical depth and scattering coefficient. This has implications to the assessment of single scattering albedo and aerosol radiative forcing on a regional scale. PMID:25199599

  5. Airborne contamination of forest soils by carbonaceous particles from industrial coal processing

    OpenAIRE

    Schmidt, M. W. I.; Knicker, Heike; Hatcher, Patrick G.; Kögel-Knabner, I.

    2000-01-01

    In the German Ruhr-area industrial coal processing emitted large amounts of carbonaceous particles for a century until 1970. Our objectives were to detect the presence of airborne carbonaceous particles and assess their impact on the chemical structure of soil organic matter in two forest soils (Podzols) with potential sources of carbonaceous particles approximately 10 to 30 km away. Contamination was not visible macroscopicaily. Organic matter was characterized in bulk soils and in particle-...

  6. Carbonaceous Aerosols Emitted from Light-Duty Vehicles Operating on Gasoline and Ethanol Fuel Blends

    Science.gov (United States)

    This study examines the chemical properties of carbonaceous aerosols emitted from three light-duty gasoline vehicles (LDVs) operating on gasoline (e0) and ethanol-gasoline fuel blends (e10 and e85). Vehicle road load simulations were performed on a chassis dynamometer using the t...

  7. Sources and composition of urban aerosol particles

    Directory of Open Access Journals (Sweden)

    M. Vogt

    2011-09-01

    Full Text Available From May 2008 to March 2009 aerosol emissions were measured using the eddy covariance method covering the size range 0.25 to 2.5 μm diameter (Dp from a 105 m tower, in central Stockholm, Sweden. Supporting chemical aerosol data were collected at roof and street level. Results show that the inorganic fraction of sulfate, nitrate, ammonium and sea salt accounts for approximately 15% of the total aerosol mass <1 μm Dp (PM1 with water soluble soil contributing 11% and water insoluble soil 47%. Carbonaceous compounds were at the most 27% of PM1 mass. It was found that heating the air from the tower to 200 °C resulted in the loss of approximately 60% of the aerosol volume at 0.25 μm Dp whereas only 40% of the aerosol volume was removed at 0.6 μm Dp. Further heating to 300 °C caused very little additional losses <0.6 μm Dp. The chemical analysis did not include carbonaceous compounds, but based on the difference between the total mass concentration and the sum of the analyzed non-carbonaceous materials, it can be assumed that the non-volatile particulate material (heated to 300 °C consists mainly of carbonaceous compounds, including elemental carbon. Furthermore, it was found that the non-volatile particle fraction <0.6 μm Dp correlated (r2 = 0.4 with the BC concentration at roof level in the city, supporting the assumption that the non-volatile material consists of carbonaceous compounds. The average diurnal cycles of the BC emissions from road traffic (as inferred from the ratio of the incremental concentrations of nitrogen oxides (NOx and BC measured on a densely trafficked street and the fluxes of non-volatile material at tower level are in close agreement, suggesting a traffic source of BC. We have estimated the emission factors (EFs for non

  8. Carbonaceous aerosols contributed by traffic and solid fuel burning at a polluted rural site in Northwestern England

    Directory of Open Access Journals (Sweden)

    D. Liu

    2010-10-01

    Full Text Available The experiment presented in this paper was conducted at the Holme Moss site, which is located in the southern Pennines region in Northwestern England during November–December 2006. The strong southwesterly wind during the experimental period, which enhanced the transport of urban pollutants from the conurbations of Greater Manchester and Liverpool, in addition to the seasonally increased nearby residential heating activities, made this site a receptor for pollutants from a range of sources. A factor analysis is applied to the mass spectra of organic matter (OM measured by the Aerodyne Aerosol Mass Spectrometer (AMS to attribute the pollutant sources. Besides the oxygenated organic aerosol (OOA, this site was found to contain a considerable fraction of primary organic aerosols (POA, mass fraction 50–70% within total mass of OM, which are source attributed as traffic emission and solid fuel burning, and are identified as hydrocarbon-like organic aerosol (HOA and solid fuel organic aerosol (SFOA respectively. There were strongly combined emissions of black carbon (BC particles from both sources, as the refractory BC component (rBC was characterized by the single particle soot photometer. This site began to be influenced during the late morning by fresh traffic emissions, whereas solid fuel burning became dominant from late afternoon until night. A covariance analysis of rBC and POA was used to derive source specific emission factors of 1.61 μgHOA/μgrBC and 1.96 μgSFOA/μgrBC. The absorbing properties of aerosols were characterized at multiple wavelengths (λ, and a stronger spectral dependence of absorption was observed when this site was significantly influenced by solid fuel burning. The rBC was estimated to contribute 3–16% of submicron aerosol mass. The single scattering albedo at λ=550 nm (SSA550 nm was significantly anti-correlated with the rBC mass fraction, but also associated with the BC mixing state. The BC

  9. Carbonaceous aerosols contributed by traffic and solid fuel burning at a polluted rural site in Northwestern England

    Directory of Open Access Journals (Sweden)

    D. Liu

    2011-02-01

    Full Text Available The experiment presented in this paper was conducted at the Holme Moss site, which is located in the southern Pennines region in Northwestern England during November–December 2006. The strong southwesterly wind during the experimental period, which enhanced the transport of urban pollutants from the conurbations of Greater Manchester and Liverpool, in addition to the seasonally increased nearby residential heating activities, made this site a receptor for pollutants from a range of sources. A factor analysis is applied to the mass spectra of organic matter (OM measured by the Aerodyne Aerosol Mass Spectrometer (AMS to attribute the pollutant sources. Besides the oxygenated organic aerosol (OOA, this site was found to contain a considerable fraction of primary organic aerosols (POA, mass fraction 50–70% within total mass of OM. The POA sources are attributed to be traffic emission and solid fuel burning, which are identified as hydrocarbon-like organic aerosol (HOA and solid fuel organic aerosol (SFOA respectively. There were strongly combined emissions of black carbon (BC particles from both sources. The refractory BC component (rBC was characterized by a single particle soot photometer. This site began to be influenced during the late morning by fresh traffic emissions, whereas solid fuel burning became dominant from late afternoon until night. A covariance analysis of rBC and POA was used to derive source specific emission factors of 1.61 μgHOA/μgrBC and 1.96 μgHOA/μgrBC. The absorbing properties of aerosols were characterized at multiple wavelengths (λ, and a stronger spectral dependence of absorption was observed when this site was significantly influenced by solid fuel burning. The rBC was estimated to contribute 3–16% of submicron aerosol mass. The single scattering albedo at λ = 700 nm (SSA700 nm was significantly anti-correlated with the rBC mass fraction, but also associated with the BC mixing state. The BC

  10. Physiochemical properties of carbonaceous aerosol from agricultural residue burning: Density, volatility, and hygroscopicity

    Science.gov (United States)

    Li, Chunlin; Hu, Yunjie; Chen, Jianmin; Ma, Zhen; Ye, Xingnan; Yang, Xin; Wang, Lin; Wang, Xinming; Mellouki, Abdelwahid

    2016-09-01

    Size-resolved effective density, mixing state, and hygroscopicity of smoke particles from five kinds of agricultural residues burning were characterized using an aerosol chamber system, including a volatility/hygroscopic tandem differential mobility analyzer (V/H-TDMA) combined with an aerosol particle mass analyzer (APM). To profile relationship between the thermodynamic properties and chemical compositions, smoke PM1.0 and PM2.5 were also measured for the water soluble inorganics, mineral elements, and carbonaceous materials like organic carbon (OC) and elemental carbon (EC). Smoke particle has a density of 1.1-1.4 g cm-3, and hygroscopicity parameter (κ) derived from hygroscopic growth factor (GF) of the particles ranges from 0.20 to 0.35. Size- and fuel type-dependence of density and κ are obvious. The integrated effective densities (ρ) and hygroscopicity parameters (κ) both scale with alkali species, which could be parameterized as a function of organic and inorganic mass fraction (forg &finorg) in smoke PM1.0 and PM2.5: ρ-1 =finorg · ρinorg-1 +forg · ρorg-1 and κ =finorg ·κinorg +forg ·κorg . The extrapolated values of ρinorg and ρorg are 2.13 and 1.14 g cm-3 in smoke PM1.0, while the characteristic κ values of organic and inorganic components are about 0.087 and 0.734, which are similar to the bulk density and κ calculated from predefined chemical species and also consistent with those values observed in ambient air. Volatility of smoke particle was quantified as volume fraction remaining (VFR) and mass fraction remaining (MFR). The gradient temperature of V-TDMA was set to be consistent with the splitting temperature in the OC-EC measurement (OC1 and OC2 separated at 150 and 250 °C). Combing the thermogram data and chemical composition of smoke PM1.0, the densities of organic matter (OM1 and OM2 correspond to OC1 and OC2) are estimated as 0.61-0.90 and 0.86-1.13 g cm-3, and the ratios of OM1/OC1 and OM2/OC2 are 1.07 and 1.29 on average

  11. Sources and characteristics of carbonaceous aerosols at Agra "World heritage site" and Delhi "capital city of India".

    Science.gov (United States)

    Pipal, A S; Tiwari, S; Satsangi, P G; Taneja, Ajay; Bisht, D S; Srivastava, A K; Srivastava, M K

    2014-01-01

    Agra, one of the oldest cities "World Heritage site", and Delhi, the capital city of India are both located in the border of Indo-Gangetic Plains (IGP) and heavily loaded with atmospheric aerosols due to tourist place, anthropogenic activities, and its topography, respectively. Therefore, there is need for monitoring of atmospheric aerosols to perceive the scenario and effects of particles over northern part of India. The present study was carried out at Agra (AGR) as well as Delhi (DEL) during winter period from November 2011 to February 2012 of fine particulate (PM₂.₅: d < 2.5 μm) as well as associated carbonaceous aerosols. PM₂.₅ was collected at both places using medium volume air sampler (offline measurement) and analyzed for organic carbon (OC) and elemental carbon (EC). Also, simultaneously, black carbon (BC) was measured (online) at DEL. The average mass concentration of PM₂.₅ was 165.42 ± 119.46 μg m(-3) at AGR while at DEL it was 211.67 ± 41.94 μg m(-3) which is ~27% higher at DEL than AGR whereas the BC mass concentration was 10.60 μg m(-3). The PM₂.₅ was substantially higher than the annual standard stipulated by central pollution control board and United States Environmental Protection Agency standards. The average concentrations of OC and EC were 69.96 ± 34.42 and 9.53 ± 7.27 μm m(-3), respectively. Total carbon (TC) was 79.01 ± 38.98 μg m(-3) at AGR, while it was 50.11 ± 11.93 (OC), 10.67 ± 3.56 μg m(-3) (EC), and 60.78 ± 14.56 μg m(-3) (TC) at DEL. The OC/EC ratio was 13.75 at (AGR) and 5.45 at (DEL). The higher OC/EC ratio at Agra indicates that the formation of secondary organic aerosol which emitted from variable primary sources. Significant correlation between PM₂.₅ and its carbonaceous species were observed indicating similarity in sources at both sites. The average concentrations of secondary organic carbon (SOC) and primary organic carbon (POC) at AGR were 48.16 and 26

  12. Impact of anthropogenic emissions and open biomass burning on regional carbonaceous aerosols in South China

    International Nuclear Information System (INIS)

    Carbonaceous aerosols were studied at three background sites in south and southwest China. Hok Tsui in Hong Kong had the highest concentrations of carbonaceous aerosols (OC = 8.7 ± 4.5 μg/m3, EC = 2.5 ± 1.9 μg/m3) among the three sites, and Jianfeng Mountains in Hainan Island (OC = 5.8 ± 2.6 μg/m3, EC = 0.8 ± 0.4 μg/m3) and Tengchong mountain over the east edge of the Tibetan Plateau (OC = 4.8 ± 4.0 μg/m3, EC = 0.5 ± 0.4 μg/m3) showed similar concentration levels. Distinct seasonal patterns with higher concentrations during the winter, and lower concentrations during the summertime were observed, which may be caused by the changes of the regional emissions, and monsoon effects. The industrial and vehicular emissions in East, Southeast and South China, and the regional open biomass burning in the Indo-Myanmar region of Asia were probably the two major potential sources for carbonaceous matters in this region. - Anthropogenic emissions in China and open biomass burning in the Indo-Myanmar region were the two major potential sources for carbonaceous matters in South China region.

  13. Impact of anthropogenic emissions and open biomass burning on regional carbonaceous aerosols in South China

    Energy Technology Data Exchange (ETDEWEB)

    Zhang Gan, E-mail: zhanggan@gig.ac.c [State Key Laboratory of Organic Geochemistry, Guangzhou Institute of Geochemistry, Chinese Academy of Sciences, Guangzhou 510640 (China); Li Jun [State Key Laboratory of Organic Geochemistry, Guangzhou Institute of Geochemistry, Chinese Academy of Sciences, Guangzhou 510640 (China); Li Xiangdong [Department of Civil and Structural Engineering, Hong Kong Polytechnic University, Hung Hom, Kowloon (Hong Kong); Xu Yue; Guo Lingli [State Key Laboratory of Organic Geochemistry, Guangzhou Institute of Geochemistry, Chinese Academy of Sciences, Guangzhou 510640 (China); Tang Jianhui [Yantai Institute of Coastal Zone Research, Chinese Academy of Sciences, Yantai 264003 (China); Lee, Celine S.L. [Department of Civil and Structural Engineering, The Hong Kong Polytechnic University, Hung Hom, Kowloon (Hong Kong); Liu Xiang [State Key Laboratory of Organic Geochemistry, Guangzhou Institute of Geochemistry, Chinese Academy of Sciences, Guangzhou 510640 (China); Chen Yingjun [Yantai Institute of Coastal Zone Research, Chinese Academy of Sciences, Yantai 264003 (China)

    2010-11-15

    Carbonaceous aerosols were studied at three background sites in south and southwest China. Hok Tsui in Hong Kong had the highest concentrations of carbonaceous aerosols (OC = 8.7 {+-} 4.5 {mu}g/m{sup 3}, EC = 2.5 {+-} 1.9 {mu}g/m{sup 3}) among the three sites, and Jianfeng Mountains in Hainan Island (OC = 5.8 {+-} 2.6 {mu}g/m{sup 3}, EC = 0.8 {+-} 0.4 {mu}g/m{sup 3}) and Tengchong mountain over the east edge of the Tibetan Plateau (OC = 4.8 {+-} 4.0 {mu}g/m{sup 3}, EC = 0.5 {+-} 0.4 {mu}g/m{sup 3}) showed similar concentration levels. Distinct seasonal patterns with higher concentrations during the winter, and lower concentrations during the summertime were observed, which may be caused by the changes of the regional emissions, and monsoon effects. The industrial and vehicular emissions in East, Southeast and South China, and the regional open biomass burning in the Indo-Myanmar region of Asia were probably the two major potential sources for carbonaceous matters in this region. - Anthropogenic emissions in China and open biomass burning in the Indo-Myanmar region were the two major potential sources for carbonaceous matters in South China region.

  14. Source apportionment of PM2.5 carbonaceous aerosol in Baghdad, Iraq

    Science.gov (United States)

    Hamad, Samera Hussein; Schauer, James Jay; Heo, Jongbae; Kadhim, Ahmed K. H.

    2015-04-01

    Baghdad is the second largest city in the Middle East and suffers from severe air quality degradation due to the high levels of the atmospheric particulate matter (PM). Limited information exists regarding the sources of PM in Baghdad, and the lack of information on sources inhibits the development of control strategies to reduce air pollution. To better understand the nature of fine particulate matter (PM2.5) in Baghdad and the Middle East, a one year sampling campaign to collect PM2.5 was conducted from September 2012 through September 2013, missing August 2013 samples due to the security situation. 24-hour integrated samples collected on a 1-in-6 day schedule were analyzed for the major components, and monthly average samples were analyzed by gas chromatography mass spectrometry (GCMS) methods to measure particle-phase organic molecular markers. The results of organic molecular markers were used in a chemical mass balance (CMB) model to quantify the sources of PM2.5 organic carbon (OC) and PM2.5 mass. Primary sources accounted for 44% of the measured PM2.5, and secondary sources were estimated to make up 28% of the measured PM2.5. Picene, a tracer of coal combustion detected in Baghdad where there is no evidence for coal combustion, can be attributed to burning crude oil and other low quality fuels in Baghdad. Source apportionment results showed that the dominant sources of the carbonaceous aerosols in Baghdad are gasoline (37 ± 6%) and diesel engines (17 ± 3%) which can be attributed to the extensive use of gasoline and diesel powered generators in Baghdad. Wood burning and residual oil combustion contributed to 5 ± 0.4 and 1 ± 0.2% respectively of OC. The unresolved sources contributed to 42 ± 19% of the OC which represented the secondary organic aerosol (SOA) and the unidentified sources.

  15. Climate response due to carbonaceous aerosols and aerosol-induced SST effects in NCAR community atmospheric model CAM3.5

    Directory of Open Access Journals (Sweden)

    W.-C. Hsieh

    2013-08-01

    Full Text Available This study used the Community Atmospheric Model 3.5 (CAM3.5 to investigate the effects of carbonaceous aerosols on climate. The simulations include control runs with 3 times the mass of carbonaceous aerosols as compared to the model's default carbonaceous aerosol mass, as well as no-carbon runs in which carbonaceous aerosols were removed. The slab ocean model (SOM and the fixed sea surface temperature (SST were used to examine effects of ocean boundary conditions. Throughout this study, climate response induced by aerosol forcing was mainly analyzed in the following three terms: (1 aerosol radiative effects under fixed SST, (2 effects of aerosol-induced SST feedbacks, and (3 total effects including effects of aerosol forcing and SST feedbacks. The change of SST induced by aerosols has large impacts on distribution of climate response; the magnitudes in response patterns such as temperature, precipitation, zonal winds, mean meridional circulation, radiative fluxes, and cloud coverage are different between the SOM and fixed SST runs. Moreover, different spatial responses between the SOM and fixed SST runs can also be seen in some local areas. This implies the importance of SST feedbacks on simulated climate response. The aerosol dimming effects cause a cooling predicted at low layers near the surface in most carbonaceous aerosol source regions. The temperature response shows a warming (cooling predicted in the north (south high latitudes, suggesting that aerosol forcing can cause climate change in regions far away from its origins. Our simulation results show that direct and semidirect radiative forcing due to carbonaceous aerosols decreases rainfall in the tropics. This implies that carbonaceous aerosols have possibly strong influence on weakening of the tropical circulation. Most changes in precipitation are negatively correlated with changes of radiative fluxes at the top of model. The changes in radiative fluxes at top of model are physically

  16. Carbonaceous aerosols in PM10 and pollution gases in winter in Beijing

    Institute of Scientific and Technical Information of China (English)

    ZHANG Ren-Jian; CAO Jun-ji; LEE Shun-cheng; SHEN Zhen-xing; HO Kin-Fai

    2007-01-01

    An intensive observation of organic carbon (OC) and element carbon (EC) in PM10 and gaseous materials (SO2, CO, and O3,) was conducted continuously to assess the characteristics of wintertime carbonaceous aerosols in an urban area of Beijing, China. Results showed that the averaged total carbon (TC) and PM10 concentrations in observation period are 30.2±120.4 and 172.6±198.3 μ/m3, respectively. Average OC concentration in nighttime (24.9±19.6 μ/m3) was 40% higher than that in daytime (17.7±10.9 μ/m3). Average EC concentrations in daytime (8.8±15.2 μ/m3) was close to that in nighttime (8.9±15.1 μ/m3). The OC/EC ratios in nighttime ranging from 2.4 to 2.7 are higher than that in daytime ranging from 1.9 to 2.0. The concentrations of OC, EC, PM10 were low with strong winds and high with weak winds. The OC and EC were well correlated with PM10, CO and SO2, which implies they have similar sources. OC and EC were not well correlated with O3. By considering variation of OC/EC ratios in daytime and night time, correlations between OC and O3, and meteorological condition, we speculated that OC and EC in Beijing PM10 were emitted as the primary particulate form. Emission of motor vehicle with low OC/EC ratio and coal combustion sources with high OC/EC ratio are probably the dominant sources for carbonaceous aerosols in Beijing in winter. A simple method was used to estimate the relative contribution of sources to carbonaceous aerosols in Beijing PM10. Motor vehicle source accounts for 80% and 68%, while coal combustion accounts for 20% and 32% in daytime and nighttime, respectively in Beijing. Averagely, the motor vehicle and coal combustion accounted for 74% and 26%, respectively, for carbonaceous aerosols during the observation period. It points to the motor vehicle is dominant emission for carbonaceous aerosols in Beijing PM10 in winter period, which should be paid attention to control high level of PM10 in Beijing effectively.

  17. Characteristics of carbonaceous aerosols emitted from peatland fire in Riau, Sumatra, Indonesia

    Science.gov (United States)

    Fujii, Yusuke; Iriana, Windy; Oda, Masafumi; Puriwigati, Astiti; Tohno, Susumu; Lestari, Puji; Mizohata, Akira; Huboyo, Haryono Setiyo

    2014-04-01

    Biomass burning is a significant source of fine particulate matter (PM2.5). Forest, bush, and peat fires in Kalimantan and Sumatra, Indonesia are major sources of transboundary haze pollution in Southeast Asia. However, limited data exist regarding the chemical characteristics of aerosols at sources. We conducted intensive field studies in Riau Province, Sumatra, Indonesia, during the peatland fire and non-burning seasons in 2012. We characterized PM2.5 carbonaceous aerosols emitted from peatland fire based on ground-based source-dominated sampling. PM2.5 aerosols were collected with two mini-volume samplers using Teflon and quartz fiber filters. Background aerosols were also sampled during the transition period between the non-burning and fire seasons. We analyzed the carbonaceous content (organic carbon (OC) and elemental carbon (EC)) by a thermal optical reflectance utilizing the IMPROVE_A protocol and the major organic components of the aerosols by a gas chromatography/mass spectrometry. PM2.5 aerosols emitted from peatland fire were observed in high concentrations of 7120 ± 3620 μg m-3 and were primarily composed of OC (71.0 ± 5.11% of PM2.5 mass). Levoglucosan exhibited the highest total ion current and was present at concentrations of 464 ± 183 μg m-3. The OC/EC ratios (36.4 ± 9.08), abundances of eight thermally-derived carbon fractions, OC/Levoglucosan ratios (10.6 ± 1.96), and Levoglucosan/Mannosan ratios (10.6 ± 2.03) represent a signature profile that is inherent in peatland fire. These data will be useful in identifying contributions from single or multiple species in atmospheric aerosol samples collected from peatland fires.

  18. Carbonaceous aerosols and pollutants over Delhi urban environment: Temporal evolution, source apportionment and radiative forcing

    International Nuclear Information System (INIS)

    Particulate matter (PM2.5) samples were collected over Delhi, India during January to December 2012 and analysed for carbonaceous aerosols and inorganic ions (SO42− and NO3−) in order to examine variations in atmospheric chemistry, combustion sources and influence of long-range transport. The PM2.5 samples are measured (offline) via medium volume air samplers and analysed gravimetrically for carbonaceous (organic carbon, OC; elemental carbon, EC) aerosols and inorganic ions (SO42− and NO3−). Furthermore, continuous (online) measurements of PM2.5 (via Beta-attenuation analyser), black carbon (BC) mass concentration (via Magee scientific Aethalometer) and carbon monoxide (via CO-analyser) are carried out. PM2.5 (online) range from 18.2 to 500.6 μg m−3 (annual mean of 124.6 ± 87.9 μg m−3) exhibiting higher night-time (129.4 μg m−3) than daytime (103.8 μg m−3) concentrations. The online concentrations are 38% and 28% lower than the offline during night and day, respectively. In general, larger night-time concentrations are found for the BC, OC, NO3−and SO42−, which are seasonally dependent with larger differences during late post-monsoon and winter. The high correlation (R2 = 0.74) between OC and EC along with the OC/EC of 7.09 (day time) and 4.55 (night-time), suggest significant influence of biomass-burning emissions (burning of wood and agricultural waste) as well as secondary organic aerosol formation during daytime. Concentrated weighted trajectory (CWT) analysis reveals that the potential sources for the carbonaceous aerosols and pollutants are local emissions within the urban environment and transported smoke from agricultural burning in northwest India during post-monsoon. BC radiative forcing estimates result in very high atmospheric heating rates (~ 1.8–2.0 K day−1) due to agricultural burning effects during the 2012 post-monsoon season. - Highlights: • Very high PM2.5 (> 200 µg m−3) levels over Delhi during agricultural

  19. Carbonaceous aerosols and pollutants over Delhi urban environment: Temporal evolution, source apportionment and radiative forcing

    Energy Technology Data Exchange (ETDEWEB)

    Bisht, D.S. [Indian Institute of Tropical Meteorology, New Delhi (India); Dumka, U.C., E-mail: dumka@aries.res.in [Aryabhatta Research Institute of Observational Sciences, Nainital (India); Kaskaoutis, D.G. [School of Natural Sciences, Shiv Nadar University, Tehsil Dadri (India); Pipal, A.S. [Department of Chemistry, Savitribai Phule Pune University, Pune (India); Srivastava, A.K. [Indian Institute of Tropical Meteorology, New Delhi (India); Soni, V.K.; Attri, S.D.; Sateesh, M. [India Meteorology Department, Lodhi Road, New Delhi (India); Tiwari, S. [Indian Institute of Tropical Meteorology, New Delhi (India)

    2015-07-15

    Particulate matter (PM{sub 2.5}) samples were collected over Delhi, India during January to December 2012 and analysed for carbonaceous aerosols and inorganic ions (SO{sub 4}{sup 2−} and NO{sub 3}{sup −}) in order to examine variations in atmospheric chemistry, combustion sources and influence of long-range transport. The PM{sub 2.5} samples are measured (offline) via medium volume air samplers and analysed gravimetrically for carbonaceous (organic carbon, OC; elemental carbon, EC) aerosols and inorganic ions (SO{sub 4}{sup 2−} and NO{sub 3}{sup −}). Furthermore, continuous (online) measurements of PM{sub 2.5} (via Beta-attenuation analyser), black carbon (BC) mass concentration (via Magee scientific Aethalometer) and carbon monoxide (via CO-analyser) are carried out. PM{sub 2.5} (online) range from 18.2 to 500.6 μg m{sup −3} (annual mean of 124.6 ± 87.9 μg m{sup −3}) exhibiting higher night-time (129.4 μg m{sup −3}) than daytime (103.8 μg m{sup −3}) concentrations. The online concentrations are 38% and 28% lower than the offline during night and day, respectively. In general, larger night-time concentrations are found for the BC, OC, NO{sub 3}{sup −}and SO{sub 4}{sup 2−}, which are seasonally dependent with larger differences during late post-monsoon and winter. The high correlation (R{sup 2} = 0.74) between OC and EC along with the OC/EC of 7.09 (day time) and 4.55 (night-time), suggest significant influence of biomass-burning emissions (burning of wood and agricultural waste) as well as secondary organic aerosol formation during daytime. Concentrated weighted trajectory (CWT) analysis reveals that the potential sources for the carbonaceous aerosols and pollutants are local emissions within the urban environment and transported smoke from agricultural burning in northwest India during post-monsoon. BC radiative forcing estimates result in very high atmospheric heating rates (~ 1.8–2.0 K day{sup −1}) due to agricultural burning effects

  20. Characteristics of carbonaceous aerosols: Impact of biomass burning and secondary formation in summertime in a rural area of the North China Plain.

    Science.gov (United States)

    Yao, Lan; Yang, Lingxiao; Chen, Jianmin; Wang, Xinfeng; Xue, Likun; Li, Weijun; Sui, Xiao; Wen, Liang; Chi, Jianwei; Zhu, Yanhong; Zhang, Junmei; Xu, Caihong; Zhu, Tong; Wang, Wenxing

    2016-07-01

    To determine the characteristics of carbonaceous aerosols in rural areas of the North China Plain, field measurements were conducted at Yucheng (YC) in the summers of 2013 and 2014. The concentrations of carbonaceous aerosols at YC exhibited clear diurnal variation, with higher concentrations in the early morning and at night and lower concentrations during the afternoon hours. The mass-balance method designed for particulate matter smaller than 2.5μm (PM2.5) was used to calculate the organic matter (OM)/organic carbon (OC) ratio. The value obtained, 2.07±0.05, was suggested as a reference to estimate organics in PM2.5 in rural areas of the North China Plain. Biomass burning was identified to be a significant source of carbonaceous aerosols; approximately half of the samples obtained at YC were affected by biomass burning during summer 2013. Case studies revealed that biomass burning accounted for up to 52.6% of the OC and 51.1% of the elemental carbon in PM2.5 samples. The organic coatings observed on sulphur-rich and potassium-rich particles indicated the formation of secondary organic aerosols (SOA) from the oxidation of precursor volatile organic compounds (VOCs) during the aging of smoke released from biomass burning. Based on the evolution of the VOCs, the contribution of VOCs oxidation to SOA concentration was 3.21 and 1.07μgm(-3)ppm(-1) CO under conditions of low nitrogen oxide (NOx) and high NOx, respectively. Aromatics (e.g. benzene, toluene, xylene and ethylbenzene) made the greatest contribution to SOA concentration (88.4% in low-NOx conditions and 80.6% in high-NOx conditions). The results of the study offer novel insights into the effects of biomass burning on the carbonaceous aerosols and SOA formation in polluted rural areas. PMID:27031303

  1. A Modeling Study of the Effects of Direct Radiative Forcing Due to Carbonaceous Aerosol on the Climate in East Asia

    Institute of Scientific and Technical Information of China (English)

    ZHANG Hua; WANG Zhili; GUO Pinwen; WANG Zaizhi

    2009-01-01

    The study investigated the effects of global direct radiative forcing due to carbonaceous aerosol on the climate in East Asia, using the CAM3 developed by NCAR. The results showed that carbonaceous aerosols cause negative forcing at the top of the atmosphere (TOA) and surface under clear sky conditions, but positive forcing at the TOA and weak negative forcing at the surface under all sky conditions. Hence, clouds could change the sign of the direct radiative forcing at the TOA, and weaken the forcing at the surface. Carbonaceous aerosols have distinct effects on the summer climate in East Asia. In southern China and India, it caused the surface temperature to increase, but the total cloud cover and precipitation to decrease. However, the opposite effects are caused for most of northern China and Bangladesh. Given the changes in temperature, vertical velocity, and surface streamflow caused by carbonaceous aerosol in this simulation, carbonaceous aerosol could also induce summer precipitation to decrease in southern China but increase in northern China.

  2. Aerosol chemical characterization and role of carbonaceous aerosol on radiative effect over Varanasi in central Indo-Gangetic Plain

    Science.gov (United States)

    Tiwari, S.; Dumka, U. C.; Kaskaoutis, D. G.; Ram, Kirpa; Panicker, A. S.; Srivastava, M. K.; Tiwari, Shani; Attri, S. D.; Soni, V. K.; Pandey, A. K.

    2016-01-01

    This study investigates the chemical composition of PM10 aerosols at Varanasi, in the central Indo-Gangetic Plain (IGP) during April to July 2011, with emphasis on examining the contribution of elemental carbon (EC) to the estimates of direct aerosol radiative effect (DARE). PM10 samples are analysed for carbonaceous aerosols (Organic Carbon, OC and EC) and water-soluble ionic species (WSIS: Cl-, SO42-, NO3-, PO42- NH4+, Na+, K+, Mg2+ and Ca2+) and several diagnostic ratios (OC/EC, K+/EC, etc) have been also used for studying the aerosol sources at Varanasi. PM10 mass concentration varies between 53 and 310 μg m-3 (mean of 168 ± 73 μg m-3), which is much higher than the National and International air quality standards. The OC mass concentration varies from 6 μg m-3 to 24 μg m-3 (mean of 12 ± 5 μg m-3; 7% of PM10 mass), whereas EC ranges between 1.0 and 14.3 μg m-3 (4.4 ± 3.9 μg m-3; ˜3% of PM10 mass). The relative low OC/EC of 3.9 ± 2.0 and strong correlation (R2 = 0.82) between them suggest the dominance of primary carbonaceous aerosols. The contribution of WSIS to PM10 is found to be ˜12%, out of which ˜57% and 43% are anions and cations, respectively. The composite DARE estimates via SBDART model reveal significant radiative effect and atmospheric heating rates (0.9-2.3 K day-1). Although the EC contributes only ˜3% to the PM10 mass, its contribution to the surface and atmospheric forcing is significantly high (37-63% and 54-77%, respectively), thus playing a major role in climate implications over Varanasi.

  3. Overview of the 2010 Carbonaceous Aerosols and Radiative Effects Study (CARES)

    Energy Technology Data Exchange (ETDEWEB)

    Zaveri, R. A.; Shaw, W. J.; Cziczo, D. J.; Schmid, B.; Ferrare, R. A.; Alexander, M. L.; Alexandrov, M.; Alvarez, R. J.; Arnott, W. P.; Atkinson, D. B.; Baidar, S.; Banta, R. M.; Barnard, J. C.; Beranek, J.; Berg, L. K.; Brechtel, F.; Brewer, W. A.; Cahill, J. F.; Cairns, B.; Cappa, C. D.; Chand, D.; China, S.; Comstock, J. M.; Dubey, M. K.; Easter, R. C.; Erickson, M. H.; Fast, J. D.; Floerchinger, C.; Flowers, B. A.; Fortner, E.; Gaffney, J. S.; Gilles, M. K.; Gorkowski, K.; Gustafson, W. I.; Gyawali, M.; Hair, J.; Hardesty, R. M.; Harworth, J. W.; Herndon, S.; Hiranuma, N.; Hostetler, C.; Hubbe, J. M.; Jayne, J. T.; Jeong, H.; Jobson, B. T.; Kassianov, E. I.; Kleinman, L. I.; Kluzek, C.; Knighton, B.; Kolesar, K. R.; Kuang, C.; Kubátová, A.; Langford, A. O.; Laskin, A.; Laulainen, N.; Marchbanks, R. D.; Mazzoleni, C.; Mei, F.; Moffet, R. C.; Nelson, D.; Obland, M. D.; Oetjen, H.; Onasch, T. B.; Ortega, I.; Ottaviani, M.; Pekour, M.; Prather, K. A.; Radney, J. G.; Rogers, R. R.; Sandberg, S. P.; Sedlacek, A.; Senff, C. J.; Senum, G.; Setyan, A.; Shilling, J. E.; Shrivastava, M.; Song, C.; Springston, S. R.; Subramanian, R.; Suski, K.; Tomlinson, J.; Volkamer, R.; Wallace, H. W.; Wang, J.; Weickmann, A. M.; Worsnop, D. R.; Yu, X. -Y.; Zelenyuk, A.; Zhang, Q.

    2012-01-01

    Substantial uncertainties still exist in the scientific understanding of the possible interactions between urban and natural (biogenic) emissions in the production and transformation of atmospheric aerosol and the resulting impact on climate change. The U.S. Department of Energy (DOE) Atmospheric Radiation Measurement (ARM) program’s Carbonaceous Aerosol and Radiative Effects Study (CARES) carried out in June 2010 in Central Valley, California, was a comprehensive effort designed to improve this understanding. The primary objective of the field study was to investigate the evolution of secondary organic and black carbon aerosols and their climate-related properties in the Sacramento urban plume as it was routinely transported into the forested Sierra Nevada foothills area. Urban aerosols and trace gases experienced significant physical and chemical transformations as they mixed with the reactive biogenic hydrocarbons emitted from the forest. Two heavily-instrumented ground sites – one within the Sacramento urban area and another about 40 km to the northeast in the foothills area – were set up to characterize the evolution of meteorological variables, trace gases, aerosol precursors, aerosol size, composition, and climate-related properties in freshly polluted and “aged” urban air. On selected days, the DOE G-1 aircraft was deployed to make similar measurements upwind and across the evolving Sacramento plume in the morning and again in the afternoon. The NASA B-200 aircraft, carrying remote sensing instruments, was also deployed to characterize the vertical and horizontal distribution of aerosols and aerosol optical properties within and around the plume. This overview provides: a) the scientific background and motivation for the study, b) the operational and logistical information pertinent to the execution of the study, c) an overview of key observations and initial findings from the aircraft and ground-based sampling platforms, and d) a roadmap of

  4. Performance of a diffusion denuder for the elimination of sampling artifacts for carbonaceous aerosols at urban and forested sites in Europe

    Czech Academy of Sciences Publication Activity Database

    Maenhaut, W.; Chi, X.; Viana, M.; Mikuška, Pavel; Večeřa, Zbyněk

    Thessaloniki, 2008. -. [European Aerosol Conference 2008. 24.08.2008-29.08.2008, Thessaloniki] Institutional research plan: CEZ:AV0Z40310501 Keywords : filter sampling artifacts * diffusion denuder * carbonaceous aerosol Subject RIV: CB - Analytical Chemistry, Separation

  5. Springtime warming and reduced snow cover from carbonaceous particles

    Directory of Open Access Journals (Sweden)

    M. G. Flanner

    2008-11-01

    Full Text Available Boreal spring climate is uniquely susceptible to solar warming mechanisms because it has expansive snow cover and receives relatively strong insolation. Carbonaceous particles can influence snow coverage by warming the atmosphere, reducing surface-incident solar energy (dimming, and reducing snow reflectance after deposition (darkening. We apply a range of models and observations to explore impacts of these processes on springtime climate, drawing several conclusions: 1 Nearly all atmospheric particles (those with visible-band single-scatter albedo less than 0.999, including all mixtures of black carbon (BC and organic matter (OM, increase net solar heating of the atmosphere-snow column. 2 Darkening caused by small concentrations of particles within snow exceeds the loss of absorbed energy from concurrent dimming, thus increasing solar heating of snowpack as well (positive net surface forcing. Over global snow, we estimate 6-fold greater surface forcing from darkening than dimming, caused by BC+OM. 3 Equilibrium climate experiments suggest that fossil fuel and biofuel emissions of BC+OM induce 95% as much springtime snow cover loss over Eurasia as anthropogenic carbon dioxide, a consequence of strong snow-albedo feedback and large BC+OM emissions from Asia. 4 Of 22 climate models contributing to the IPCC Fourth Assessment Report, 21 underpredict the rapid warming (0.64°C decade−1 observed over springtime Eurasia since 1979. Darkening from natural and anthropogenic sources of BC and mineral dust exerts 3-fold greater forcing on springtime snow over Eurasia (3.9 W m−2 than North America (1.2 W m−2. Inclusion of this forcing significantly improves simulated continental warming trends, but does not reconcile the low bias in rate of Eurasian spring snow cover decline exhibited by all models.

  6. Carbonaceous aerosols in megacity Xi'an, China: Implications of thermal/optical protocols comparison

    Science.gov (United States)

    Han, Y. M.; Chen, L.-W. A.; Huang, R.-J.; Chow, J. C.; Watson, J. G.; Ni, H. Y.; Liu, S. X.; Fung, K. K.; Shen, Z. X.; Wei, C.; Wang, Q. Y.; Tian, J.; Zhao, Z. Z.; Prévôt, André S. H.; Cao, J. J.

    2016-05-01

    Carbonaceous aerosol is an important component that influences the environment, climate, and human health. Organic and elemental carbon (OC and EC) are the two main constituents of carbonaceous aerosols that have opposite, i.e., cooling versus warming, effects on the Earth's radiation balance. Knowledge on the variability of OC/EC splits measured by different thermal/optical protocols is useful for understanding the uncertainty in the climate models. This study shows good correlations within OC or EC (r2 > 0.83, P < 0.001) across the IMPROVE, IMPROVE_A, and EUSAAR_2 protocols for both ambient aerosol samples and biomass burning samples. However, EC concentrations differ by more than two folds, and OC/EC ratios differ up to a factor of 2.7. The discrepancies were attributed to the selection between the reflectance and transmittance corrections and the different peak inert-atmosphere temperature. The IMPROVE and IMPROVE_A protocols also quantified different char and soot concentrations, two subtypes of EC with distinct chemical and optical properties. Char, but not soot, was found to correlate with the humic-like substances (HULIS) content in the samples, suggesting that both char and HULIS originate mainly from biomass burning. A one-year (2012-2013) ambient aerosol monitoring in Xi'an, China, shows that OC, EC, and char displayed winter highs and summer lows, while soot had no seasonal trend. The char/soot ratios showed a "single peak" in winter, while OC/EC ratios exhibited "dual peak" feature due to the influence of secondary organic aerosol formation. In addition to commonly measured OC and EC, we recommend both char and soot from a common reference method to be considered in the chemical transport and climate models.

  7. Global climate impacts of country-level primary carbonaceous aerosol from solid-fuel cookstove emissions

    Science.gov (United States)

    Lacey, Forrest; Henze, Daven

    2015-11-01

    Cookstove use is globally one of the largest unregulated anthropogenic sources of primary carbonaceous aerosol. While reducing cookstove emissions through national-scale mitigation efforts has clear benefits for improving indoor and ambient air quality, and significant climate benefits from reduced green-house gas emissions, climate impacts associated with reductions to co-emitted black (BC) and organic carbonaceous aerosol are not well characterized. Here we attribute direct, indirect, semi-direct, and snow/ice albedo radiative forcing (RF) and associated global surface temperature changes to national-scale carbonaceous aerosol cookstove emissions. These results are made possible through the use of adjoint sensitivity modeling to relate direct RF and BC deposition to emissions. Semi- and indirect effects are included via global scaling factors, and bounds on these estimates are drawn from current literature ranges for aerosol RF along with a range of solid fuel emissions characterizations. Absolute regional temperature potentials are used to estimate global surface temperature changes. Bounds are placed on these estimates, drawing from current literature ranges for aerosol RF along with a range of solid fuel emissions characterizations. We estimate a range of 0.16 K warming to 0.28 K cooling with a central estimate of 0.06 K cooling from the removal of cookstove aerosol emissions. At the national emissions scale, countries’ impacts on global climate range from net warming (e.g., Mexico and Brazil) to net cooling, although the range of estimated impacts for all countries span zero given uncertainties in RF estimates and fuel characterization. We identify similarities and differences in the sets of countries with the highest emissions and largest cookstove temperature impacts (China, India, Nigeria, Pakistan, Bangladesh and Nepal), those with the largest temperature impact per carbon emitted (Kazakhstan, Estonia, and Mongolia), and those that would provide the

  8. Global climate impacts of country-level primary carbonaceous aerosol from solid-fuel cookstove emissions

    International Nuclear Information System (INIS)

    Cookstove use is globally one of the largest unregulated anthropogenic sources of primary carbonaceous aerosol. While reducing cookstove emissions through national-scale mitigation efforts has clear benefits for improving indoor and ambient air quality, and significant climate benefits from reduced green-house gas emissions, climate impacts associated with reductions to co-emitted black (BC) and organic carbonaceous aerosol are not well characterized. Here we attribute direct, indirect, semi-direct, and snow/ice albedo radiative forcing (RF) and associated global surface temperature changes to national-scale carbonaceous aerosol cookstove emissions. These results are made possible through the use of adjoint sensitivity modeling to relate direct RF and BC deposition to emissions. Semi- and indirect effects are included via global scaling factors, and bounds on these estimates are drawn from current literature ranges for aerosol RF along with a range of solid fuel emissions characterizations. Absolute regional temperature potentials are used to estimate global surface temperature changes. Bounds are placed on these estimates, drawing from current literature ranges for aerosol RF along with a range of solid fuel emissions characterizations. We estimate a range of 0.16 K warming to 0.28 K cooling with a central estimate of 0.06 K cooling from the removal of cookstove aerosol emissions. At the national emissions scale, countries’ impacts on global climate range from net warming (e.g., Mexico and Brazil) to net cooling, although the range of estimated impacts for all countries span zero given uncertainties in RF estimates and fuel characterization. We identify similarities and differences in the sets of countries with the highest emissions and largest cookstove temperature impacts (China, India, Nigeria, Pakistan, Bangladesh and Nepal), those with the largest temperature impact per carbon emitted (Kazakhstan, Estonia, and Mongolia), and those that would provide the

  9. Feasibility study for GCOM-C/SGLI: Retrieval algorithms for carbonaceous aerosols

    Science.gov (United States)

    Mukai, Sonoyo; Sano, Itaru; Yasumoto, Masayoshi; Fujito, Toshiyuki; Nakata, Makiko; Kokhanovsky, Alexander

    2016-04-01

    The Japan Aerospace Exploration Agency (JAXA) has been developing the new Earth observing system, GCOM (Global Change Observation Mission) project, which consists of two satellite series of GCOM-W1 and GCOM-C1. The 1st GCOM-C satellite will board the SGLI (second generation global imager) which also includes polarimetric sensor and be planed to launch in early of 2017. The SGLI has multi (19)-channels including near UV channel (380 nm) and two polarization channels at red and near-infrared wavelengths of 670 and 870 nm. EUMETSAT plans to collect polarization measurements with a POLDER follow on 3MI / EPS-SG in 2021. Then the efficient retrieval algorithms for aerosol and/or cloud based on the combination use of radiance and polarization are strongly expected. This work focuses on serious biomass burning episodes in East Asia. It is noted that the near UV measurements are available for detection of the carbonaceous aerosols. The biomass burning aerosols (BBA) generated by forest fire and/or agriculture biomass burning have influenced on the severe air pollutions. It is known that the forest fire increases due to global warming and a climate change, and has influences on them vice versa. It is well known that this negative cycle decreases the quality of global environment and human health. We intend to consider not only retrieval algorithms of remote sensing for severe air pollutions but also detection and/or distinction of aerosols and clouds, because mixture of aerosols and clouds are often occurred in the severe air pollutions. Then precise distinction of aerosols and clouds, namely aerosols in cloudy scenes and/or clouds in heavy aerosol episode, is desired. Aerosol retrieval in the hazy atmosphere has been achieved based on radiation simulation method of successive order of scattering 1,2. In this work, we use both radiance and polarization measurements observed by GLI and POLDER-2 on Japanese ADEOS-2 satellite in 2003 as a simulated data. As a result the

  10. AEROSOL PARTICLE COLLECTOR DESIGN STUDY

    Energy Technology Data Exchange (ETDEWEB)

    Lee, S; Richard Dimenna, R

    2007-09-27

    A computational evaluation of a particle collector design was performed to evaluate the behavior of aerosol particles in a fast flowing gas stream. The objective of the work was to improve the collection efficiency of the device while maintaining a minimum specified air throughput, nominal collector size, and minimal power requirements. The impact of a range of parameters was considered subject to constraints on gas flow rate, overall collector dimensions, and power limitations. Potential improvements were identified, some of which have already been implemented. Other more complex changes were identified and are described here for further consideration. In addition, fruitful areas for further study are proposed.

  11. Carbonaceous aerosols and mineral dust in atmospheric outflow from the Indo-Gangetic Plain

    Science.gov (United States)

    Sarin, M.; Srinivas, B.; Rengarajan, R.

    2012-12-01

    Atmospheric carbonaceous aerosols and mineral dust over south and south-east Asia has been a subject of major debate over the past two decades because of their potential impact on the regional air quality and climate forcing. A comprehensive study through ground-based measurements and data-base for aerosol chemical composition (involving both organic and inorganic constituents) is, thus, essential to constrain the large uncertainties associated with the climate impact. Our systematic study from a downwind site (Kharagpur: 22.02N, 87.11E) in the Indo-Gangetic Plain (IGP) suggests large temporal variability in the atmospheric mass concentrations of mineral dust, organic and elemental carbon (OC, EC), water-soluble organic carbon (WSOC) and inorganic species (WSIS). This is attributed to seasonally varying anthropogenic emissions, their source strength, boundary layer dynamics, secondary aerosol formation and long-range transport of mineral dust from desert regions. Based on diagnostic ratios [OC/EC ≈ 7.0 ± 2.2, WSOC/OC ≈ 0.6 and K+/EC ≈ 0.48 ± 0.17], we document biomass burning emissions (wood-fuel and post-harvest agricultural-waste burning) as a major source of carbonaceous aerosols. The characteristic ratios: nss-SO42-/EC (3.9 ± 2.1), nss-SO42-/OC (0.61 ± 0.46), high abundance of SO42- (6.9 - 25.3 μg m-3) and SO42-/ΣWSIS = 45 - 77 % in the outflow provide better assessment of aerosol optical properties. The subsequent downwind transport of pollutants from the IGP significantly influences the chemical composition of aerosols over the Bay of Bengal. The dominance of aerosol SO42- in the marine atmospheric boundary layer (MABL) is evident from the wide-spread depletion of chloride with respect to sea-salt composition. The Ca/Al and Fe/Al ratios in the IGP-outflow, used as a proxy for the long-range transport of mineral dust, are consistent with those in the MABL. The mass closure for PM2.5 composition suggests that contribution of mineral dust (20

  12. Springtime warming and reduced snow cover from carbonaceous particles

    Directory of Open Access Journals (Sweden)

    M. G. Flanner

    2009-04-01

    Full Text Available Boreal spring climate is uniquely susceptible to solar warming mechanisms because it has expansive snow cover and receives relatively strong insolation. Carbonaceous particles can influence snow coverage by warming the atmosphere, reducing surface-incident solar energy (dimming, and reducing snow reflectance after deposition (darkening. We apply a range of models and observations to explore impacts of these processes on springtime climate, drawing several conclusions: 1 Nearly all atmospheric particles (those with visible-band single-scatter albedo less than 0.999, including all mixtures of black carbon (BC and organic matter (OM, increase net solar heating of the atmosphere-snow column. 2 Darkening caused by small concentrations of particles within snow exceeds the loss of absorbed energy from concurrent dimming, thus increasing solar heating of snowpack as well (positive net surface forcing. Over global snow, we estimate 6-fold greater surface forcing from darkening than dimming, caused by BC+OM. 3 Equilibrium climate experiments suggest that fossil fuel and biofuel emissions of BC+OM induce 95% as much springtime snow cover loss over Eurasia as anthropogenic carbon dioxide, a consequence of strong snow-albedo feedback and large BC+OM emissions from Asia. 4 Of 22 climate models contributing to the IPCC Fourth Assessment Report, 21 underpredict the rapid warming (0.64°C decade−1 observed over springtime Eurasia since 1979. Darkening from natural and anthropogenic sources of BC and mineral dust exerts 3-fold greater forcing on springtime snow over Eurasia (3.9 W m−2 than North America (1.2 W m−2. Inclusion of this forcing significantly improves simulated continental warming trends, but does not reconcile the low bias in rate of Eurasian spring snow cover decline exhibited by all models, likely because BC deposition trends are negative or near-neutral over much of Eurasia. Improved Eurasian

  13. Dating recent lake sediments using spheroidal carbonaceous particle (SCP)

    Institute of Scientific and Technical Information of China (English)

    WU Yanhong; WANG Sumin; XIA Weilan; LIU Jian

    2005-01-01

    Dating lake sediment using sedimentary event is the supplement and calibration to traditional dating by radionuclide such as 210Pb and 137Cs. Based on the change of spheroidal carbonaceous particle (SCP) concentration, the age sequence of lake sediments can be deduced. It is one of the dating methods using sedimentary event. SCP is formed from combustion of fossil fuel at high temperature up to 1750℃ and at a rate of heating of approaching 104 ℃/s. It can be dispersed to several hundred kilometers away from its source and deposited with precipitation or dryly deposited, and kept in sediments. Compared with Cs or Pb, there is no evidence for SCP that it decays in lake sediments and is un-removable once stored except by physical disturbance because it is mainly composed of element carbon. Handy method to extract, identify and calculate has been developed. Although fossil fuel has been used early in China, combustion at high temperature started later since emergence of electricity generation. The productivity of SCP is positively related with the generated thermal power, which is reflected as the SCP concentration in lake sediments increases with the increase of generated thermal power. Therefore, reliable sediment markers from the start of the SCP record and the remarkable variation can be used for dating purpose. In China, electricity industry started from the 1950s, and rapid increase of generated power took place since 1978. Based on these time markers, SCP time sequences of lake sediment cores LH and LL-4 from Longgan Lake, the middle reach of the Yangtze River, have been established, which is comparable with the results from 137Cs and 210Pb, and has eliminated the errors of dating using 137Cs and 210Pb.

  14. Carbonaceous aerosols and pollutants over Delhi urban environment: Temporal evolution, source apportionment and radiative forcing.

    Science.gov (United States)

    Bisht, D S; Dumka, U C; Kaskaoutis, D G; Pipal, A S; Srivastava, A K; Soni, V K; Attri, S D; Sateesh, M; Tiwari, S

    2015-07-15

    Particulate matter (PM2.5) samples were collected over Delhi, India during January to December 2012 and analysed for carbonaceous aerosols and inorganic ions (SO4(2-) and NO3(-)) in order to examine variations in atmospheric chemistry, combustion sources and influence of long-range transport. The PM2.5 samples are measured (offline) via medium volume air samplers and analysed gravimetrically for carbonaceous (organic carbon, OC; elemental carbon, EC) aerosols and inorganic ions (SO4(2-) and NO3(-)). Furthermore, continuous (online) measurements of PM2.5 (via Beta-attenuation analyser), black carbon (BC) mass concentration (via Magee scientific Aethalometer) and carbon monoxide (via CO-analyser) are carried out. PM2.5 (online) range from 18.2 to 500.6μgm(-3) (annual mean of 124.6±87.9μgm(-3)) exhibiting higher night-time (129.4μgm(-3)) than daytime (103.8μgm(-3)) concentrations. The online concentrations are 38% and 28% lower than the offline during night and day, respectively. In general, larger night-time concentrations are found for the BC, OC, NO3(-)and SO4(2-), which are seasonally dependent with larger differences during late post-monsoon and winter. The high correlation (R(2)=0.74) between OC and EC along with the OC/EC of 7.09 (day time) and 4.55 (night-time), suggest significant influence of biomass-burning emissions (burning of wood and agricultural waste) as well as secondary organic aerosol formation during daytime. Concentrated weighted trajectory (CWT) analysis reveals that the potential sources for the carbonaceous aerosols and pollutants are local emissions within the urban environment and transported smoke from agricultural burning in northwest India during post-monsoon. BC radiative forcing estimates result in very high atmospheric heating rates (~1.8-2.0Kday(-1)) due to agricultural burning effects during the 2012 post-monsoon season. PMID:25864155

  15. Characterization of carbonaceous aerosols during the MINOS campaign in Crete, July–August 2001: a multi-analytical approach

    Directory of Open Access Journals (Sweden)

    J. Sciare

    2003-01-01

    these two methods for determining BC brings here new insights on the origin of carbonaceous aerosols in a complex mixture of different sources. It brings also to our attention that important deviations in BC levels are observed using three widely used EGA's techniques and most probably none of the EGA tested here are well adapted to fully characterize this aerosol mixture. Spherical, smooth and silico-aluminated fly-ash observed by an Analytical Scanning Electron Microscope (ASEM confirm the influence of coal combustion on the carbonaceous aerosol load throughout the campaign. A rough calculation based on a BC/nss-SO4 mass ratio suggests that biomass burning could be responsible for half of the BC concentration recorded during the MINOS campaign. From the plot of BC as a function of TC, two linear correlations were observed corresponding to 2 times series (before and after 12 August. Such good correlations suggest, from a first look, that both BC and OC have similar origin and atmospheric transport. On the other hand, the plot of BC as a function of TC obtained from the 2-step thermal method applied to DEKATI Low Pressure Cascade Impactor samples does not show a similar correlation and points out a non conservative distribution of this ratio with 2 super micron modes enriched in OC, correlated with sea salt aerosols and probably originating from gas-to-particle conversion.

  16. Characterization of carbonaceous aerosols during the MINOS campaign in Crete, July–August 2001: a multi-analytical approach

    Directory of Open Access Journals (Sweden)

    R. Sarda-Estève

    2003-07-01

    between these two methods for determining BC brings here new insights on the origin of carbonaceous aerosols in a complex mixture of different sources. It brings also to our attention that important deviations in BC levels are observed using three widely used EGA techniques and most probably none of the EGA tested here are well adapted to fully characterize this aerosol mixture. Spherical, smooth and silico-aluminated fly-ash observed by Analytical Scanning Electron Microscope (ASEM confirm the influence of coal combustion on the carbonaceous aerosol load throughout the campaign. A raw calculation based on BC/nss-SO4 mass ratio suggests that biomass burning could be responsible for half of the BC concentration recorded during the MINOS campaign. From the plot of BC as a function of TC, two linear correlations were observed corresponding to 2 times series (before and after 12 August. Such good correlations suggest, from a first look, that both BC and OC have similar origin and atmospheric transport. On the other hand, the plot of BC as a function of TC obtained from the 2-step thermal method applied to DEKATI Low Pressure Cascade Impactor samples does not show a similar correlation and points out a non conservative distribution of this ratio with 2 super micron modes enriched in OC, correlated with sea salt aerosols and probably originating from gas-to-particle conversion.

  17. Aerosol-Assisted Self-Assembly of Reticulated N-Doped Carbonaceous Submicron Spheres for Effective Removal of Hexavalent Chromium.

    Science.gov (United States)

    He, Jiawei; Long, Yuan; Wang, Yiyan; Wei, Chaoliang; Zhan, Jingjing

    2016-07-01

    This Research Article described a facile one-step method to prepare reticulated N-doped carbonaceous submicron spheres. Through a simple aerosol-assisted technology, glucosamine sulfate used as a carbon source was aerosolized and carbonized to functionalized carbonaceous submicron spheres. The electrostatic attraction between protonated amino groups and sulfate in the aerosol droplets induced a self-assembly and led to the formation of reticular structure, avoiding the use of templates. Compared to bare carbonaceous materials produced from glucose, reticulated N-doped carbonaceous spheres exhibit higher efficiency in the removal of Cr(VI), where the doping of element nitrogen led to electrostatic attraction between protonated nitrogen and chromium ions, and reticulated structure created relatively higher surface area and pore volume, facilitating materials to contact with Cr(VI) ions. XPS characterization proved these novel N-doped carbonaceous materials could effectively transform Cr(VI) to less toxic Cr(III) because of the surface reducing groups. For the practical application, several factors including the initial pH, materials dosage and recycle numbers on the removal performance were studied. PMID:27299376

  18. Carbonaceous aerosols on the south edge of the Tibetan Plateau: concentrations, seasonality and sources

    Directory of Open Access Journals (Sweden)

    Z. Cong

    2014-10-01

    Full Text Available To quantitatively evaluate the effect of carbonaceous aerosols on the south edge of the Tibetan Plateau, aerosol samples were collected weekly from August 2009 to July 2010 at Mt. Everest (Qomolangma Station for Atmospheric and Environmental Observation and Research, briefly QOMS, 28.36° N, 86.95° E, 4276 m a.s.l.. The samples were analyzed for organic carbon (OC, elemental carbon (EC, water-soluble organic carbon (WSOC and major ions. The average concentrations of OC, EC and WSOC were 1.43, 0.25 and 0.77 μg m−3, respectively. The concentration levels of OC and EC at QOMS are comparable to those at high elevation sites on the southern slopes of the Himalayas (Langtang and NCO-P, but three to six times lower than those at Manora Peak, India and Godavari, Nepal. Sulfate was the most abundant anion species followed by nitrate, accounting for 25 and 12% of total ionic mass, respectively. Ca2+ was the most abundant cation species (annual average of 0.88 μg m−3. The various aerosol compositions showed distinctive seasonality. The dust loading, represented by Ca2+ concentration, was relatively constant throughout the year. While OC, EC and other ionic species (NH4+, K+, NO3−, and SO42− exhibited a pronounced peak in the pre-monsoon period and a minimum in the monsoon season. Similar seasonal trends of aerosol composition were also reported previously from the southern slope of the Himalayas, such as Langtang and NCO-P. This phenomenon indicates that both slopes of Himalayas share a common atmospheric environment regime. The strong correlation of OC and EC in QOMS aerosols with K+ and levoglucosan indicates that they were mainly originated from biomass burning. The active fire spots observed by MODIS and their backward trajectories further demonstrate that in pre-monsoon season, agricultural and forest fires in the northern India and Nepal were most likely sources of carbonaceous aerosol at QOMS. In addition to large-scale atmospheric

  19. Carbonaceous aerosol determination in Valenzuela City using a thermal-optical technique

    International Nuclear Information System (INIS)

    Carbonaceous aerosol, broadly classified into organic carbon (OC) and elemental carbon (EC), are atmospheric particulates known to have significant effects to health, climate and visibility. Concentrations of organic carbon and elemental carbon in the PM2.5 range were measured for Valenzuela City, Metro Manila (Philippines) from September 2011 to August 2012. The method employed was thermal-optical reflectance (TOR) following the IMPROVEA protocol. Results show that OC (8.00 ug/m3) and EC (6.63 ug/m3) contributed 21.0% and 17.4%, respectively to the whole PM2.5 mass. Carbonaceous aerosol in total, therefore, accounted for about 38.4% of the total fine particulate matter. Compared to cities of neighboring countries in Asia, the OC level of Valenzuela City is generally intermediate while EC levels are higher than the most, resulting in one of the lowest OC/EC ratios in the region of about 1.21. This suggests minimal secondary organic aerosol formation and the dominance of combustion sources which are probably less efficient (e.g. greater diesel and two-stroke engine contribution) compared to that of the other countries. Time series comparison of EC with black carbon (BC) levels obtained through reflectometry, a method currently used for monitoring in the country, also shows a generally good agreement between the two methods. There are specific days however, that obtained values are far from each other, lowering the correlation of the two parameters (r2 = 0.33). This is likely due to the presence of other light-absorbing particulates other than EC. Further efforts are necessary to better understand the relationship between these quantities and the cause of deviations. (author)

  20. The distribution of PM10 and PM2.5 carbonaceous aerosol in Baotou, China

    Science.gov (United States)

    Zhou, Haijun; He, Jiang; Zhao, Boyi; Zhang, Lijun; Fan, Qingyun; Lü, Changwei; Dudagula; Liu, Tao; Yuan, Yinghui

    2016-09-01

    Particulate matter (PM), including PM10 and PM2.5, is one of the major impacts on air quality, visibility, climate change, earth radiation balance, and public health. Organic carbon (OC) and elemental carbon (EC) are the major components of PM. 804 samples (PM10 and PM2.5) were simultaneously collected from six urban sites covering 3 districts in Baotou, in January, April, September, and November 2014. As to a long-term study on the effects of carbonaceous aerosol, data were collected annually at Environmental Protection Agency of Baotou (EPB). The concentrations of PM10 and PM2.5, the spatial distribution and content of OC and EC, the relationship between OC and EC, and the formation of secondary organic carbon (SOC) have been investigated. The findings indicated that the concentrations of these particle matter are higher than that in US or European standards. The average concentrations of OC in PM10 and PM2.5 follow the order: January > November > April > September; and for EC in PM10 and PM2.5 follow the order: January > November > September > April. Affected by metrological factors, it was indicated that high wind speed and low relative humidity were beneficial for removal of OC and EC in January and November. Pearson correlations and cluster analysis on OC and EC concentrations in PM10 and PM2.5 with gaseous pollutants (SO2, NO2, and CO) suggested that OC shared the same emission sources with SO2 and CO from combustion, while EC's sources mainly came from vehicles exhaust and combustion which contributed to NO2 as well. The OC concentration is mainly primary in warm months, while it appears secondary in cold months in Baotou. There is a common characteristic among the cities with higher SOC in winter, wherever the coal combustion can lead to the severe pollution. This work is important for the construction of the database of OC and EC concentrations in PM10 and PM2.5 at spatial and time intervals, and it can provide scientific suggestion for similar PM

  1. Better constraints on sources of carbonaceous aerosols using a combined 14C – macro tracer analysis in a European rural background site

    Directory of Open Access Journals (Sweden)

    S. Henne

    2011-01-01

    Full Text Available The source contributions to carbonaceous PM2.5 aerosol were investigated at a European background site at the edge of the Po Valley, in Northern Italy, during the period January–December 2007. Carbonaceous aerosol was described as the sum of eight source components: primary (1 and secondary (2 biomass burning organic carbon, biomass burning elemental carbon (3, primary (4 and secondary (5 fossil fuel burning organic carbon, fossil fuel burning elemental carbon (6, primary (7 and secondary (8 biogenic organic carbon. The concentration of each component was quantified using a set of macro tracers (organic carbon OC, elemental carbon EC, and levoglucosan, micro tracers (arabitol and mannitol, and 14C measurements. This was the first time that 14C measurements were performed on a long time series of data able to represent the entire annual cycle. This set of 6 tracers, together with assumed uncertainty ranges of the ratios of OC-to-EC, and the fraction of modern carbon in the 8 source categories, provides strong constraints to the source contributions to carbonaceous aerosol. The uncertainty of contributions was assessed with a Quasi-Monte Carlo (QMC method accounting for the variability of OC and EC emission factors, and the uncertainty of reference fractions of modern carbon. During winter biomass burning composed 50% of the total carbon (TC concentration, while in summer secondary biogenic OC accounted for 45% of TC. The contribution of primary biogenic aerosol particles was negligible during the entire year. Moreover, aerosol associated with fossil fuel burning represented 26% and 43% of TC in winter and summer, respectively. The comparison of source apportionment results in different urban and rural areas showed that the sampling site was mainly affected by local aerosol sources during winter and regional air masses from the nearby Po Valley in summer. This observation was further confirmed by back-trajectory analysis applying the Potential

  2. Better constraints on sources of carbonaceous aerosols using a combined 14C – macro tracer analysis in a European rural background site

    Directory of Open Access Journals (Sweden)

    S. Henne

    2011-06-01

    Full Text Available The source contributions to carbonaceous PM2.5 aerosol were investigated at a European background site at the edge of the Po Valley, in Northern Italy, during the period January–December 2007. Carbonaceous aerosol was described as the sum of 8 source components: primary (1 and secondary (2 biomass burning organic carbon, biomass burning elemental carbon (3, primary (4 and secondary (5 fossil organic carbon, fossil fuel burning elemental carbon (6, primary (7 and secondary (8 biogenic organic carbon. The mass concentration of each component was quantified using a set of macro tracers (organic carbon OC, elemental carbon EC, and levoglucosan, micro tracers (arabitol and mannitol, and 14C measurements. This was the first time that 14C measurements covered a full annual cycle with daily resolution. This set of 6 tracers, together with assumed uncertainty ranges of the ratios of OC-to-EC, and the reference fraction of modern carbon in the 8 source categories, provides strong constraints to the source contributions to carbonaceous aerosol. The uncertainty of contributions was assessed with a Quasi-Monte Carlo (QMC method accounting for the variability of OC and EC emission factors, the uncertainty of reference fractions of modern carbon, and the measurement uncertainty. During winter, biomass burning composed 64 % (±15 % of the total carbon (TC concentration, while in summer secondary biogenic OC accounted for 50 % (±16 % of TC. The contribution of primary biogenic aerosol particles was negligible during the entire year. Moreover, aerosol associated with fossil sources represented 27 % (±16 % and 41 % (±26 % of TC in winter and summer, respectively. The contribution of secondary organic aerosol (SOA to the organic mass (OM was significant during the entire year. SOA accounted for 30 % (±16 % and 85 % (±12 % of OM during winter and summer, respectively. While the summer SOA was dominated by biogenic sources, winter SOA was mainly due to biomass

  3. Estimation of lifetime of carbonaceous aerosol from open crop residue burning during Mount Tai Experiment 2006 (MTX2006

    Directory of Open Access Journals (Sweden)

    X. L. Pan

    2012-06-01

    Full Text Available Studying the emission ratios of carbonaceous aerosols (element carbon, EC, and organic carbon, OC from open biomass burning helps to reduce uncertainties in emission inventories and provides necessary constraints for model simulations. We measured apparent elemental carbon (ECa and OC concentrations at the summit of Mount Tai (Mt. Tai during intensive open crop residue burning (OCRB episodes using a Sunset OCEC analyzer. Equivalent black carbon (BCe concentrations were determined using a Multiple Angle Absorption Photometer (MAAP. In the fine particle mode, OC and EC showed strong correlations (r > 0.9 with carbon monoxide (CO. Footprint analysis using the FLEXPART_WRF model indicated that OCRB in central east China (CEC had a significant influence on ambient carbonaceous aerosol loadings at the summit of Mt. Tai. ΔECa/ΔCO ratios resulting from OCRB plumes were 14.3 ± 1.0 ng m−3 ppbv−1 at Mt. Tai. This ratio was more than three times those resulting from urban pollution in CEC, demonstrating that significant concentrations of soot particles were released from OCRB. ΔOC/ΔCO ratio from fresh OCRB plumes was found to be 41.9 ± 2.6 ng m−3 ppbv−1 in PM1. The transport time of smoke particles was estimated using the FLEXPART_WRF tracer model by releasing inert particles from the ground layer inside geographical regions where large numbers of hotspots were detected by a MODIS satellite sensor. Fitting regressions using the e-folding exponential function indicated that the removal efficiency of OC (normalized to CO was much larger than that of ECa mass, with mean lifetimes of 27 h (1.1 days for OC and 105 h (4.3 days for ECa, respectively. The lifetime of black carbon estimated for the OCRB events in east China was comparably lower than the values normally adopted in the transport models. Short lifetime of organic carbon

  4. Simulating the formation of carbonaceous aerosol in a European Megacity (Paris) during the Megapoli summer and winter campaigns

    NARCIS (Netherlands)

    Fountoukis, C.; Megaritis, A.G.; Skyllakou, K.; Charalampidis, P.E.; Denier van der Gon, H.A.C.; Crippa, M.; Prevot, A.S.H.; Fachinger, F.; Wiedensohler, A.; Pilinis, C.; Pandis, S.N.

    2016-01-01

    We use a three-dimensional regional chemical transport model (PMCAMx) with high grid resolution and high-resolution emissions (4 x 4 km2) over the Paris greater area to simulate the formation of carbonaceous aerosol dur-ing a summer (July 2009) and a winter (January/February 2010) period as part of

  5. Climate response due to carbonaceous aerosols and aerosol-induced SST effects in NCAR community atmospheric model CAM3.5

    Directory of Open Access Journals (Sweden)

    W.-C. Hsieh

    2013-03-01

    Full Text Available This study used Community Atmospheric Model 3.5 (CAM3.5 to investigate the effects of carbonaceous aerosols on climate. The simulations include control runs with carbonaceous aerosols and no carbon runs in which carbonaceous aerosols were removed. The Slab Ocean Model (SOM and the fixed Sea Surface Temperature (SST were used to examine effects of ocean boundary conditions. Throughout this study, climate response induced by aerosol forcing was mainly analyzed in the following three terms: (1 aerosol radiative effects under fixed SST, (2 effects of aerosol-induced SST feedbacks , and (3 total effects including effects of aerosol forcing and SST feedbacks. The change of SST induced by aerosols has large impacts on distribution of climate response, the magnitudes in response patterns such as temperature, precipitation, zonal winds, mean meridional circulation, radiative fluxes and cloud coverage are different between the SOM and fixed SST runs. Moreover, different spatial responses between the SOM and fixed SST runs can also be seen in some local areas. This implies the importance of SST feedbacks on simulated climate response. The aerosol dimming effects cause a cooling predicted at low layers near the surface in most of carbonaceous aerosol source regions. The temperature response shows a warming (cooling predicted in the north (south high latitudes, suggesting that aerosol forcing can cause climate change in regions far away from its origins. Our simulation results show that warming of the troposphere due to black carbon decreases rainfall in the tropics. This implies that black carbon has possibly strong influence on weakening of the tropical circulation. Most of these changes in precipitation are negatively correlated with changes of radiative fluxes at the top of model. The changes in radiative fluxes at top of model are physically consistent with the response patterns in cloud fields. On global average, low-level cloud coverage increases, mid

  6. Black carbon or brown carbon? The nature of light-absorbing carbonaceous aerosols

    Directory of Open Access Journals (Sweden)

    M. O. Andreae

    2006-01-01

    Full Text Available Although the definition and measurement techniques for atmospheric 'black carbon' ('BC' or 'elemental carbon'' ('EC' have long been subjects of scientific controversy, the recent discovery of light-absorbing carbon that is not black ('brown carbon, Cbrown' makes it imperative to reassess and redefine the components that make up light-absorbing carbonaceous matter (LAC in the atmosphere. Evidence for the atmospheric presence of Cbrown comes from (1 spectral aerosol light absorption measurements near specific combustion sources, (2 observations of spectral properties of water extracts of continental aerosol, (3 laboratory studies indicating the formation of light-absorbing organic matter in the atmosphere, and (4 indirectly from the chemical analogy of aerosol species to colored natural humic substances. We show that brown carbon may severely bias measurements of 'BC' and 'EC' over vast parts of the troposphere, especially those strongly polluted by biomass burning, where the mass concentration of Cbrown is high relative to that of soot carbon. Chemical measurements to determine 'EC' are biased by the refractory nature of Cbrown as well as by complex matrix interferences. Optical measurements of 'BC' suffer from a number of problems: (1 many of the presently used instruments introduce a substantial bias into the determination of aerosol light absorption, (2 there is no unique conversion factor between light absorption and 'EC' or 'BC' concentration in ambient aerosols, and (3 the difference in spectral properties between the different types of LAC, as well as the chemical complexity of Cbrown, lead to several conceptual as well as practical complications. We also suggest that due to the sharply increasing absorption of Cbrown towards the UV, single-wavelength light absorption measurements may not be adequate for the assessment of absorption of solar radiation in the troposphere. We discuss the possible consequences of these effects for our

  7. Black carbon or brown carbon? The nature of light-absorbing carbonaceous aerosols

    Directory of Open Access Journals (Sweden)

    M. O. Andreae

    2006-05-01

    Full Text Available Although the definition and measurement methods of atmospheric ''black carbon'' (''BC'' have long been subjects of scientific controversy, the recent discovery of light-absorbing carbon that is not black (''brown carbon, Cbrown'' makes it imperative to reassess and redefine the components that make up light-absorbing carbonaceous matter (LAC in the atmosphere. Evidence for the atmospheric presence of Cbrown comes directly from aerosol absorption measurements near specific combustion sources, from observations of spectral properties of water extracts of continental aerosol, from laboratory studies indicating the formation of light-absorbing organic matter in the atmosphere, and indirectly from the chemical analogy of aerosol species to colored natural humic substances. We show that these species may severely bias measurements of ''BC'' and ''EC'' over vast parts of the troposphere, where mass concentration of Cbrown is high relative to that of combustion soot. We also imply that due to the strongly skewed absorption of Cbrown towards the UV, single-wavelength light absorption measurements may not be adequate for the assessment of absorption of solar radiation in the troposphere. The possible consequences of these effects on our understanding of tropospheric processes are discussed.

  8. Characteristics and sources of PM2.5-bound carbonaceous aerosols in the Yangtze River Delta, China

    Science.gov (United States)

    Hong, Youwei; Hong, Zhenyu; Chen, Jinsheng

    2016-04-01

    An investigation of atmospheric fine particle (PM2.5) from Shanghai, Nanjing and Ningbo in the Yangtze River Delta was conducted during Nov 2014 and Aug 2015. Organic species, including 16 polycyclic aromatic hydrocarbons (PAHs), 10 nitro-PAHs and C8 to C40 n-alkanes, and stable carbon isotopes OC (δ13COC) and EC (δ13CEC) were used to evaluate carbonaceous aerosols' spatiotemporal variations and identify their potential sources. The averaged concentrations of total PAHs and n-alkanes in Shanghai, Nanjing and Ningbo were 16.5 and 101.1 ng m-3, 21.1 and 128.2 ng m-3, 33.0 and 241.1 ng m-3, respectively, while the mean concentrations of 10 nitro-PAHs was 2.02, 2.37 and 2.70 ng m-3. Seasonal variations of organic compounds were listed in the following order: winter > autumn > spring > summer. N-alkanes detected in PM2.5 were characterized by odd carbon number preference, with a unimodal peak shape. The maximum carbon number (Cmax) was C29, followed by C27 and C31. According to diagnostic ratios and principle components analysis (PCA) methods, vehicle emissions and coal burning were the dominant sources of PAHs. The ratios of 2-nitrofluoranthene to 1-nitropyrene were larger than 5, indicating that atmospheric transformation from PAHs was a major source of nitro-PAHs. Meanwhile, primary emissions tracers i.e., 1-nitropyrene (the mean concentration of 0.024 ng m-3 in all cities) was observed, suggesting primary contribution of motor vehicle exhaust to the fine particulate organic aerosols. In addition, isotope abundances (δ13COC=‑24.6±0.8‰ and δ13CEC = ‑23.9±1.4‰) and EC/TC ratio (0.2 < EC/TC < 0.5) in Shanghai demonstrated that fossil fuels (e.g. motor vehicles) were the most important source for carbonaceous PM2.5. We further focus on radiocarbon (14C) analysis and gas/particle partitioning of organic tracers on different size particles. Keywords: organic tracers; stable carbon isotopes; spatiotemporal variations; sources apportionment; Yangtze River Delta

  9. Characteristics and sources of PM2.5-bound carbonaceous aerosols in the Yangtze River Delta, China

    Science.gov (United States)

    Hong, Youwei; Hong, Zhenyu; Chen, Jinsheng

    2016-04-01

    An investigation of atmospheric fine particle (PM2.5) from Shanghai, Nanjing and Ningbo in the Yangtze River Delta was conducted during Nov 2014 and Aug 2015. Organic species, including 16 polycyclic aromatic hydrocarbons (PAHs), 10 nitro-PAHs and C8 to C40 n-alkanes, and stable carbon isotopes OC (δ13COC) and EC (δ13CEC) were used to evaluate carbonaceous aerosols' spatiotemporal variations and identify their potential sources. The averaged concentrations of total PAHs and n-alkanes in Shanghai, Nanjing and Ningbo were 16.5 and 101.1 ng m-3, 21.1 and 128.2 ng m-3, 33.0 and 241.1 ng m-3, respectively, while the mean concentrations of 10 nitro-PAHs was 2.02, 2.37 and 2.70 ng m-3. Seasonal variations of organic compounds were listed in the following order: winter > autumn > spring > summer. N-alkanes detected in PM2.5 were characterized by odd carbon number preference, with a unimodal peak shape. The maximum carbon number (Cmax) was C29, followed by C27 and C31. According to diagnostic ratios and principle components analysis (PCA) methods, vehicle emissions and coal burning were the dominant sources of PAHs. The ratios of 2-nitrofluoranthene to 1-nitropyrene were larger than 5, indicating that atmospheric transformation from PAHs was a major source of nitro-PAHs. Meanwhile, primary emissions tracers i.e., 1-nitropyrene (the mean concentration of 0.024 ng m-3 in all cities) was observed, suggesting primary contribution of motor vehicle exhaust to the fine particulate organic aerosols. In addition, isotope abundances (δ13COC=‑24.6±0.8‰ and δ13CEC = ‑23.9±1.4‰) and EC/TC ratio (0.2 fossil fuels (e.g. motor vehicles) were the most important source for carbonaceous PM2.5. We further focus on radiocarbon (14C) analysis and gas/particle partitioning of organic tracers on different size particles. Keywords: organic tracers; stable carbon isotopes; spatiotemporal variations; sources apportionment; Yangtze River Delta

  10. Effect of Increasing Temperature on Carbonaceous Aerosol Direct Radiative Effect over Southeastern US

    Science.gov (United States)

    Mielonen, Tero; Kokkola, Harri; Hienola, Anca; Kühn, Thomas; Merikanto, Joonas; Korhonen, Hannele; Arola, Antti; Kolmonen, Pekka; Sogacheva, Larisa; de Leeuw, Gerrit

    2016-04-01

    Aerosols are an important regulator of the Earth's climate. They scatter and absorb incoming solar radiation and thus cool the climate by reducing the amount of energy reaching the atmospheric layers and the surface below (direct effect). A certain subset of the particles can also act as initial formation sites for cloud droplets and thereby modify the microphysics, dynamics, radiative properties and lifetime of clouds (indirect effects). The magnitude of aerosol radiative effects remains the single largest uncertainty in current estimates of anthropogenic radiative forcing. One of the key quantities needed for accurate estimates of anthropogenic radiative forcing is an accurate estimate of the radiative effects from natural unperturbed aerosol. The dominant source of natural aerosols over Earth's vast forested regions are biogenic volatile organic compounds (BVOC) which, following oxidation in the atmosphere, can condense onto aerosol particles to form secondary organic aerosol (SOA) and significantly modify the particles' properties. In accordance with the expected positive temperature dependence of BVOC emissions, several previous studies have shown that some aerosol properties, such as mass concentration and ability to act as cloud condensation nuclei (CCN), also correlate positively with temperature at many forested sites. There is conflicting evidence as to whether the aerosol direct effects have a temperature dependence due to increased BVOC emissions. The main objective of this study is to investigate the causes of the observed effect of increasing temperatures on the aerosol direct radiative effect, and to provide a quantitative estimate of this effect and of the resulting negative feedback in a warming climate. More specifically, we will investigate the causes of the positive correlation between aerosol optical depth (AOD) and land surface temperature (LST) over southeastern US where biogenic emissions are a significant source of atmospheric particles. In

  11. SPM analysis of single aerosol particles

    International Nuclear Information System (INIS)

    Aerosol samples were collected using Anderson cascade impact samplers and the dispersed single aerosol particles were embedded in thin PVDF films. A group of single aerosol particles distributed in an area of 180 μm x 150 μm was analyzed by the scanning proton microprobe (SPM). The distributions of 12 elements in the group were mapped with the three dimensional contour technique. Air pollution sources were then analyzed in some details. It is shown that analysis of the group of single aerosol particles by SPM may become a new approach to the study of air pollution

  12. Characteristics, seasonality and sources of carbonaceous and ionic components in the tropical Indian aerosols

    Directory of Open Access Journals (Sweden)

    C. M. Pavuluri

    2011-02-01

    Full Text Available To better characterize South and Southeast Asian aerosols, PM10 samples collected from tropical Chennai, India (13.04° N; 80.17° E were analyzed for carbonaceous and water-soluble ionic components. Concentration ranges of elemental carbon (EC and organic carbon (OC were 2.4–14 μg m−3 and 3.2–15.6 μg m−3 in winter samples whereas they were 1.1–2.5 μg m−3 and 4.1–17.6 μg m−3 in summer samples, respectively. Concentration of secondary organic carbon (SOC retrieved from EC-tracer method was 4.6 ± 2.8 μg m−3 in winter and 4.3 ± 2.8 μg m−3 in summer. SO42- (8.8 ± 2.5 μg m−3 and 4.1 ± 2.7 μg m−3 in winter and summer, respectively was found as the most abundant ionic species (57% on average, n = 49, followed by NH4+ (15% > NO3 > Cl > K+> Na+ > Ca2+ > MSA > Mg2+. The mass fractions of EC, organic matter (OM and ionic species varied seasonally, following the air mass trajectories and corresponding source strength. Based on mass concentration ratios of selected components and relations of EC and OC to marker species, we found that biofuel/biomass burning is the major source of atmospheric aerosols in South and Southeast Asia. The high concentrations of SOC and WSOC/OC ratios (ave. 0.45; n = 49 as well as good correlations between SOC and WSOC suggest that the secondary production of organic aerosols during long-range atmospheric transport is also significant in this region. This study provides the baseline data of carbonaceous aerosols for southern part of the Indian subcontinent.

  13. Seasonal variations and sources of ambient fossil and biogenic-derived carbonaceous aerosols based on 14C measurements in Lhasa, Tibet

    Science.gov (United States)

    Huang, Jie; Kang, Shichang; Shen, Chengde; Cong, Zhiyuan; Liu, Kexin; Wang, Wei; Liu, Lichao

    2010-06-01

    A total of 30 samples of total suspended particles were collected at an urban site in Lhasa, Tibet from August 2006 to July 2007 for investigating carbonaceous aerosol features. The fractions of contemporary carbon ( fc) in total carbon (TC) of ambient aerosols are presented using radiocarbon ( 14C) measurements. The value of fc represents the biogenic contribution to TC, as the biosphere releases organic compounds with the present 14C/ 12C level ( fc = 1), whereas 14C has become extinct in anthropogenic emissions of fossil carbon ( fc = 0). The fc values in Lhasa ranging from 0.357 to 0.702, are higher than Beijing and Tokyo, but clearly lower than the rural region of Launceston, which indicates a major biogenic influence in Lhasa. Seasonal variations of fc values corresponded well with variations of pollutants concentrations (e.g. NO 2). Higher fc values appeared in winter indicating carbonaceous aerosol is more dominated by wood burning and incineration of agricultural wastes within this season. The lower fc values in summer and autumn may be caused by increased diesel and petroleum emissions related to tourism in Lhasa. δ13C values ranged from - 26.40‰ to - 25.10‰, with relative higher values in spring and summer, reflecting the increment of fossil carbon emissions.

  14. Mixing state of particles with secondary species by single particle aerosol mass spectrometer in an atmospheric pollution event

    Science.gov (United States)

    Xu, Lingling; Chen, Jinsheng

    2016-04-01

    Single particle aerosol mass spectrometer (SPAMS) was used to characterize size distribution, chemical composition, and mixing state of particles in an atmospheric pollution event during 20 Oct. - 5 Nov., 2015 in Xiamen, Southeast China. A total of 533,012 particle mass spectra were obtained and clustered into six groups, comprising of industry metal (4.5%), dust particles (2.6%), carbonaceous species (70.7%), K-Rich particles (20.7%), seasalt (0.6%) and other particles (0.9%). Carbonaceous species were further divided into EC (70.6%), OC (28.5%), and mixed ECOC (0.9%). There were 61.7%, 58.3%, 4.0%, and 14.6% of particles internally mixed with sulfate, nitrate, ammonium and C2H3O, respectively, indicating that these particles had undergone significant aging processing. Sulfate was preferentially mixed with carbonaceous particles, while nitrate tended to mix with metal-containing and dust particles. Compared to clear days, the fractions of EC-, metal- and dust particles remarkably increased, while the fraction of OC-containing particles decreased in pollution days. The mixing state of particles, excepted for OC-containing particles with secondary species was much stronger in pollution days than that in clear days, which revealed the significant influence of secondary particles in atmospheric pollution. The different activity of OC-containing particles might be related to their much smaller aerodynamic diameter. These results could improve our understanding of aerosol characteristics and could be helpful to further investigate the atmospheric process of particles.

  15. Effects of fine carbonaceous particles containing high and low unpaired electron spin densities on lungs of female mice.

    Science.gov (United States)

    Repine, John E; Reiss, Oscar K; Elkins, Nancy; Chughtai, Abdul R; Smith, Dwight M

    2008-10-01

    The negative impacts on human health that accompany inhalation of atmospheric particles are documented in numerous epidemiologic studies, but the effect of specific chemical properties of the particles is generally unknown. We developed and employed technology for generating inhalable aerosols of carbonaceous air pollution particles that have specific physical and chemical properties. We find that inhaling particles with greater unpaired electron spin (free radical) densities stimulates greater lung inflammatory and oxidative stress responses. Cultured alveolar macrophages take up more particles of greater free radical content, develop mitochondrial abnormalities, and release more leukotriene B(4) (LTB(4)) than alveolar macrophages exposed to lesser free-radical-containing particles in vitro. Mice exposed to high free radical particles in vivo also develop mitochondrial abnormalities in alveolar macrophages and increased oxidative stress, which is reflected by increases in lung nitrotyrosine staining and lung lavage nitrogen oxide levels compared with those of lesser free radical density. These results provide insight for the unexplained geographic differences and have implications for fossil fuel combustion conditions and the impact of fine particles on health and disease. PMID:18940721

  16. Investigating the Use of a Diffusion Flame to Produce Black Carbon Standards for Thermal- Optical Analysis of Carbonaceous Aerosols

    Science.gov (United States)

    Ortiz Montalvo, D. L.; Kirchstetter, T. W.; Soto-García, L. L.; Mayol-Bracero, O. L.

    2006-12-01

    Combustion generated particles are a concern to both climate and public health due to their ability to scatter and absorb solar radiation and alter cloud properties, and because they are small enough to be inhaled and deposit in the lungs where they may cause respiratory and other health problems. Specific concern is focused on particles that originate from the combustion of diesel fuel. Diesels particles are composed mainly of carbonaceous material, especially in locations where diesel fuel sulfur is low. These particles are black due to the strongly light absorbing nature of the refractory carbon components, appropriately called black carbon (BC). This research project focuses on the uncertainty in the measurement of BC mass concentration, which is typically determined by analysis of particles collected on a filter using a thermal-optical analysis (TOA) method. Many studies have been conducted to examine the accuracy of the commonly used variations of the TOA method, which vary in their sample heating protocol, carrier gas, and optical measurement. These studies show that BC measurements are inaccurate due to the presence of organic carbon (OC) in the aerosols. OC may co-evolve with BC or char to form BC during analysis, both of which make it difficult to distinguish between the OC and BC in the sample. The goal of this study is to develop the capability of producing standard samples of known amounts of BC, either alone or mixed with other aerosol constituents, and then evaluate which TOA methods accurately determine the BC amount. An inverted diffusion flame of methane and air was used to produce particle samples containing only BC as well as samples of BC mixed with humic acid (HA). Our study found that HA is light absorbing and catalyzes the combustion of BC. It is expected that both of these attributes will challenge the ability of TOA methods in distinguishing between OC and BC, such as the simple two step TOA method which relies solely on temperature to

  17. Observationally-constrained carbonaceous aerosol source estimates for the Pearl River Delta area of China

    Science.gov (United States)

    Li, N.; Fu, T.-M.; Cao, J. J.; Zheng, J. Y.; He, Q. Y.; Long, X.; Zhao, Z. Z.; Cao, N. Y.; Fu, J. S.; Lam, Y. F.

    2015-11-01

    We simulated elemental carbon (EC) and organic carbon (OC) aerosols over the Pearl River Delta (PRD) area of China and compared the results to seasonal surface measurements, with the aim of quantifying carbonaceous aerosol sources from a "top-down" perspective. Our regional model was driven by current-best estimates of PRD EC (39.5 Gg C yr-1) and OC (32.8 Gg C yr-1) emissions and included updated secondary organic aerosol formation pathways. The simulated annual mean EC and OC concentrations were 4.0 and 7.7 μg C m-3, respectively, lower than the observed annual mean EC and OC concentrations (4.5 and 13.1 μg C m-3, respectively). We used multiple regression to match the simulated EC against seasonal mean observations. The resulting top-down estimate for EC emission in the PRD area was 52.9 ± 8.0 Gg C yr-1. We estimated the OC emission in the PRD area to be 60.2 ± 10.3 Gg C yr-1, based on the top-down EC emission estimate and the primary OC / EC ratios derived from bottom-up statistics. Using these top-down emission estimates, the simulated average annual mean EC and OC concentrations were improved to 4.4 and 9.5 μg C m-3, respectively, closer to the observations. Secondary sources accounted for 42 % of annual mean surface OC in our top-down simulations, with biogenic VOCs being the most important precursors.

  18. Nanoscale Polymeric Particles via Aerosol-Photopolymerization

    OpenAIRE

    Akgün, Ertan

    2015-01-01

    This PhD thesis focuses on the process of aerosol-photopolymerization for the generation of various polymeric particles. Such structures are most often prepared by liquid-based methods via the well-established thermal initiation step, and aerosol-photopolymerization is presented as an alternative, aerosol-based technique which employs photoinitiated polymerization. Discussed within this thesis are the advantages and broad aspects of the process.

  19. Characteristics of carbonaceous aerosols at a pair of suburban and downtown sites in Nanjing, China

    Science.gov (United States)

    Cui, H.; Zhang, J.; Zhao, Y.

    2014-12-01

    Carbonaceous species in PM2.5 were measured in three seasons (except winter) in downtown and around a year in suburban in Nanjing. In particular, the OC and EC concentrations were continuously measured with 1-h interval at both sites. The mean concentrations of PM2.5, OC, EC were 85.9 μg/m3, 10.4 μg/m3, 4.2 μg/m3 and 63.4 μg/m3, 8.1 μg/m3, 5.3μg/m3 for downtown and suburban respectively. At the suburban site, compared to the lowest average concentration in spring, the relatively higher concentration of carbonaceous aerosol in summer was caused by biomass-burning activities. Significant increasing peaks of OC (up to 122.9 ug/m3) and EC (up to 35.8 ug/m3) in suburban were recorded in the June 10th night, and it is indicated using back trajectory that the air mass came through nearby agriculture areas. On the other hand, the OC and EC concentrations during the 2nd AYG (Asian Youth Games, Aug 16th - 24th in 2013) compared to that in rest days in August reduced by 21% and 10%, respectively, attributing to the effective control measures on reduction of industrial point sources, temporary control of motor vehicle and fugitive dusts. Rations of OC/EC in suburban were much lower than that in downtown. This might be due to the fact that the sampling point in suburban is quite close (in 400 meters) to a main highway. Both OC and EC concentrations in suburban were higher in nighttime than daytime, except OC in summer, indicating the existence of strong SOC and supported by high OC/EC and O3 at noon. The annual average SOC estimated by EC-tracer methods occupied 34.5% and 36.7% of the total OC for the downtown and suburban areas, respectively. OC/EC correlations in suburban were much weaker than those from downtown areas, which shows suburban areas is much more affected by long-range transport of pollution and/or complex sources including domestic coal combustion, biomass burning, industrial and transportation, especially in three other seasons except winter, which is

  20. Characterization of aerosol particles at the forested site in Lithuania

    Science.gov (United States)

    Rimselyte, I.; Garbaras, A.; Kvietkus, K.; Remeikis, V.

    2009-04-01

    Atmospheric particulate matter (PM), especially fine particles (particles with aerodynamic diameter less than 1 m, PM1), has been found to play an important role in global climate change, air quality, and human health. The continuous study of aerosol parameters is therefore imperative for better understanding the environmental effects of the atmospheric particles, as well as their sources, formation and transformation processes. The particle size distribution is particularly important, since this physical parameter determines the mass and number density, lifetime and atmospheric transport, or optical scattering behavior of the particles in the atmosphere (Jaenicke, 1998). Over the years several efforts have been made to improve the knowledge about the chemical composition of atmospheric particles as a function of size (Samara and Voutsa, 2005) and to characterize the relative contribution of different components to the fine particulate matter. It is well established that organic materials constitute a highly variable fraction of the atmospheric aerosol. This fraction is predominantly found in the fine size mode in concentrations ranging from 10 to 70% of the total dry fine particle mass (Middlebrook et al., 1998). Although organic compounds are major components of the fine particles, the composition, formation mechanism of organic aerosols are not well understood. This is because particulate organic matter is part of a complex atmospheric system with hundreds of different compounds, both natural and anthropogenic, covering a wide range of chemical properties. The aim of this study was to characterize the forest PM1, and investigate effects of air mass transport on the aerosol size distribution and chemical composition, estimate and provide insights into the sources and characteristics of carbonaceous aerosols through analysis ^13C/12C isotopic ratio as a function of the aerosol particles size. The measurements were performed at the Rugšteliškis integrated

  1. Carbonaceous aerosols in the Western Mediterranean during summertime and their contribution to the aerosol optical properties at ground level: First results of the ChArMEx-ADRIMED 2013 intensive campaign in Corsica

    Science.gov (United States)

    Sciare, Jean; Dulac, Francois; Feron, Anais; Crenn, Vincent; Sarda Esteve, Roland; Baisnee, Dominique; Bonnaire, Nicolas; Hamonou, Eric; Mallet, Marc; Lambert, Dominique; Nicolas, Jose B.; Bourrianne, Thierry; Petit, Jean-Eudes; Favez, Olivier; Canonaco, Francesco; Prevot, Andre; Mocnik, Grisa; Drinovec, Luka; Marpillat, Alexandre; Serrie, Wilfrid

    2014-05-01

    As part of the Chemistry-Aerosol Mediterranean Experiment (ChArMEx, http://charmex.lsce.ipsl.fr/), the CORSiCA (http://www.obs-mip.fr/corsica) and the ANR-ADRIMED programs, a large set of real-time measurements of carbonaceous aerosols was deployed in June 2013 at the Cape Corsica atmospheric supersite (http://gaw.empa.ch/gawsis/reports.asp?StationID=2076203042). Submicron organic aerosols (OA) were monitored every 30 min using an Aerosol Chemical Speciation Monitor (ACSM; Aerodyne Res. Inc. MA, USA); Fine (PM2.5) Organic Carbon (OC) and Elemental Carbon (EC) were measured every 2h using an OCEC Sunset Field Instrument (Sunset Lab, OR, USA) and every 12h using a low-vol (Leckel) filter sampler running at 2.3m3/h. Equivalent Black Carbon (BC) was monitored using two Aethalometers (models AE31 and AE33, Magee Scientific, US & Aerosol d.o.o., Slovenia) and a MAAP instrument (Thermo). Quality control of this large dataset was performed through chemical mass closure studies (using co-located SMPS and TEOM-FDMS) and direct comparisons with other real-time instruments running in parallel (Particle-Into-Liquid-Sampler-Ion-Chromatograph for ions, filter sampling, ...). Source apportionment of OA was then performed using the SourceFinder software (SoFi v4.5, http://www.psi.ch/acsm-stations/me-2) allowing the distinction between hydrogen- and oxygen-like organic aerosols (HOA and OOA, respectively) and highlighting the major contribution of secondary OA in the Western Mediterranean during summer. Using this time-resolved chemical information, reconstruction of the optical aerosol properties were performed and compared with integrating nephelometer (Model 3563, TSI, US) and photoacoustic extinctiometer (PAX, DMT, US) measurements performed in parallel. Results of these different closure studies (chemical/physical/optical) are presented and discussed here in details. They highlight the central role of carbonaceous aerosols on the optical properties of aerosols at ground level

  2. Historical estimation of carbonaceous aerosol emissions from biomass open burning in China for the period 1990-2005

    International Nuclear Information System (INIS)

    Multi-year inventories of carbonaceous aerosol emissions from biomass open burning at a high spatial resolution of 0.5o x 0.5o have been constructed in China using GIS methodology for the period 1990-2005. Black carbon (BC) emissions have increased by 383.03% at an annual average rate of 25.54% from 14.05 Gg in 1990 to 67.87 Gg in 2005; while organic carbon (OC) emissions have increased by 365.43% from 57.37 Gg in 1990 to 267.00 Gg in 2005. Through the estimation period, OC/BC ratio for biomass burning was averagely 4.09, suggesting that it was not the preferred control source from a climatic perspective. Spatial distribution of BC and OC emissions were similar, mainly concentrated in three northeastern provinces, central provinces of Shandong, Jiangsu, Anhui and Henan, and southern provinces of Guangxi, Guangdong, Hunan and Sichuan basin, covering 24.89% of China's territory, but were responsible for 63.38% and 67.55% of national BC and OC emissions, respectively. - Highlights: → Multi-year carbonaceous aerosol emission inventory of biomass burning is established. → Spatial distribution of carbonaceous aerosol emissions is determined. → Black carbon emissions have increased by 383.03% from 1990 to 2005. → Organic carbon emissions have increased by 365.43% from 1990 to 2005. → OC/BC ratio for biomass burning was averagely 4.09 for the period 1990-2005. - Chinese multi-year carbonaceous aerosol emission inventories from biomass open burning were established for the period of 1990-2005 for the first time.

  3. A TGA/FT-IR study for OC and EC quantification applied to carbonaceous aerosol collected in Milan (Italy)

    OpenAIRE

    Fermo, P.; Piazzalunga, A.; Vecchi, R.; Valli, G.; Ceriani, M.

    2005-01-01

    Carbon analysis consists in the evaluation of the carbonaceous content of the aerosol (TC) but, more importantly, of its distribution between the two components EC (Elemental Carbon) and OC (Organic Carbon) that are characterized by different physical-chemical properties. In spite of the numerous studies focused on this topic, nowadays, a universal methodology for the determination of the two components EC and OC is not available. In fact OC and EC (also known as black carbon or soot) are ope...

  4. A review and analysis of microwave absorption in polymer composites filled with carbonaceous particles

    Science.gov (United States)

    Qin, F.; Brosseau, C.

    2012-03-01

    Carbon (C) is a crucial material for many branches of modern technology. A growing number of demanding applications in electronics and telecommunications rely on the unique properties of C allotropes. The need for microwave absorbers and radar-absorbing materials is ever growing in military applications (reduction of radar signature of aircraft, ships, tanks, and targets) as well as in civilian applications (reduction of electromagnetic interference among components and circuits, reduction of the back-radiation of microstrip radiators). Whatever the application for which the absorber is intended, weight reduction and optimization of the operating bandwidth are two important issues. A composite absorber that uses carbonaceous particles in combination with a polymer matrix offers a large flexibility for design and properties control, as the composite can be tuned and optimized via changes in both the carbonaceous inclusions (C black, C nanotube, C fiber, graphene) and the embedding matrix (rubber, thermoplastic). This paper offers a perspective on the experimental efforts toward the development of microwave absorbers composed of carbonaceous inclusions in a polymer matrix. The absorption properties of such composites can be tailored through changes in geometry, composition, morphology, and volume fraction of the filler particles. Polymer composites filled with carbonaceous particles provide a versatile system to probe physical properties at the nanoscale of fundamental interest and of relevance to a wide range of potential applications that span radar absorption, electromagnetic protection from natural phenomena (lightning), shielding for particle accelerators in nuclear physics, nuclear electromagnetic pulse protection, electromagnetic compatibility for electronic devices, high-intensity radiated field protection, anechoic chambers, and human exposure mitigation. Carbonaceous particles are also relevant to future applications that require environmentally benign and

  5. Organic composition of carbonaceous aerosols in an aged prescribed fire plume

    Directory of Open Access Journals (Sweden)

    B. Yan

    2007-12-01

    Full Text Available Aged smoke from a prescribed fire (dominated by conifers impacted Atlanta, GA on 28 February 2007 and dramatically increased hourly ambient concentrations of PM2.5 and organic carbon (OC up to 140 and 72 μg m−3, respectively. It was estimated that over 1 million residents were exposed to the smoky air lasting from the late afternoon to midnight. To better understand the processes impacting the aging of fire plumes, a detailed chemical speciation of carbonaceous aerosols was conducted by gas chromatography/mass spectrometry (GC/MS analysis. Ambient concentrations of many organic species (levoglucosan, resin acids, retene, n-alkanes, n-alkanoic acids associated with wood burning emission were significantly elevated on the event day. Levoglucosan increased by a factor of 10, while hopanes, steranes, cholesterol and major polycyclic aromatic hydrocarbons (PAHs did not show obvious increases. Strong odd over even carbon number predominance was found for n-alkanes versus even over odd predominance for n-alkanoic acids. Alteration of resin acids during transport from burning sites to monitors is suggested by the observations. Our study also suggests that large quantities of biogenic volatile organic compounds (VOCs and semivolatile organic compounds (SVOCs were released both as products of combustion and unburned vegetation heated by the fire. Higher leaf temperature can stimulate biogenic VOC and SVOC emissions, which enhanced formation of secondary organic aerosols (SOA in the atmosphere. This is supported by elevated ambient concentrations of secondary organic tracers (dicarboxylic acids, 2-methyltetrols, pinonic acid and pinic acid. An approximate source profile was built for the aged fire plume to help better understand evolution of wood smoke emission and can be used for source apportionment.

  6. Dual carbon isotope characterization of total organic carbon in wintertime carbonaceous aerosols from northern India

    Science.gov (United States)

    Bikkina, Srinivas; Andersson, August; Sarin, M. M.; Sheesley, R. J.; Kirillova, E.; Rengarajan, R.; Sudheer, A. K.; Ram, K.; Gustafsson, Örjan

    2016-05-01

    Large-scale emissions of carbonaceous aerosols (CA) from South Asia impact both regional climate and air quality, yet their sources are not well constrained. Here we use source-diagnostic stable and radiocarbon isotopes (δ13C and Δ14C) to characterize CA sources at a semiurban site (Hisar: 29.2°N, 75.2°E) in the NW Indo-Gangetic Plain (IGP) and a remote high-altitude location in the Himalayan foothills (Manora Peak: 29.4°N, 79.5°E, 1950 m above sea level) in northern India during winter. The Δ14C of total aerosol organic carbon (TOC) varied from -178‰ to -63‰ at Hisar and from -198‰ to -1‰ at Manora Peak. The absence of significant differences in the 14C-based fraction biomass of TOC between Hisar (0.81 ± 0.03) and Manora Peak (0.82 ± 0.07) reveals that biomass burning/biogenic emissions (BBEs) are the dominant sources of CA at both sites. Combining this information with δ13C, other chemical tracers (K+/OC and SO42-/EC) and air mass back trajectory analyses indicate similar source regions in the IGP (e.g., Punjab and Haryana). These results highlight that CA from BBEs in the IGP are not only confined to the atmospheric boundary layer but also extend to higher elevations of the troposphere, where the synoptic-scale circulations could substantially influence their abundances both to the Himalayas and over the downwind oceanic regions such as the Indian Ocean. Given the vast emissions of CA from postharvest crop residue combustion practices in the IGP during early Northeast Monsoon, this information is important for both improved process and model understanding of climate and health effects, as well as in guiding policy decision aiming at reducing emissions.

  7. Carbonaceous aerosols recorded in a Southeastern Tibetan glacier: variations, sources and radiative forcing

    Directory of Open Access Journals (Sweden)

    M. Wang

    2014-07-01

    Full Text Available High temporal resolution measurements of black carbon (BC and organic carbon (OC covering the time period of 1956–2006 in an ice core over the southeastern Tibetan Plateau show a distinct seasonal dependence of OC / BC ratio with higher values in the non-monsoon season than during the summer monsoon. We use a global aerosol-climate model, in which BC emitted from different source regions can be explicitly tracked, to quantify BC source-receptor relationships between four Asian source regions and the southeastern Tibetan Plateau as a receptor. The model results show that South Asia is a primary contributor during the non-monsoon season (October to May (81% and on an annual basis (74%, followed by East Asia (14% and 21%, respectively. The ice-core record also indicates stable and relatively low BC and OC deposition fluxes from late 1950s to 1980, followed by an overall increase to recent years. This trend is consistent with the BC and OC emission inventories and the fuel consumption of South Asia as the primary contributor. Moreover, the increasing trend of OC / BC ratio since the early 1990s indicates a growing contribution of coal combustion and biomass burning to the emissions. The estimated radiative forcing induced by BC and OC impurities in snow has increased since 1980, suggesting an increasing influence of carbonaceous aerosols on the Tibetan glacier melting and the availability of water resources in the surrounding regions. Our study indicates that more attention to OC is merited because of its non-negligible light absorption and the recent rapid increases evident in the ice core record.

  8. Carbonaceous aerosols recorded in a Southeastern Tibetan glacier: variations, sources and radiative forcing

    Science.gov (United States)

    Wang, M.; Xu, B.; Cao, J.; Tie, X.; Wang, H.; Zhang, R.; Qian, Y.; Rasch, P. J.; Zhao, S.; Wu, G.; Zhao, H.; Joswiak, D. R.; Li, J.; Xie, Y.

    2014-07-01

    High temporal resolution measurements of black carbon (BC) and organic carbon (OC) covering the time period of 1956-2006 in an ice core over the southeastern Tibetan Plateau show a distinct seasonal dependence of OC / BC ratio with higher values in the non-monsoon season than during the summer monsoon. We use a global aerosol-climate model, in which BC emitted from different source regions can be explicitly tracked, to quantify BC source-receptor relationships between four Asian source regions and the southeastern Tibetan Plateau as a receptor. The model results show that South Asia is a primary contributor during the non-monsoon season (October to May) (81%) and on an annual basis (74%), followed by East Asia (14% and 21%, respectively). The ice-core record also indicates stable and relatively low BC and OC deposition fluxes from late 1950s to 1980, followed by an overall increase to recent years. This trend is consistent with the BC and OC emission inventories and the fuel consumption of South Asia as the primary contributor. Moreover, the increasing trend of OC / BC ratio since the early 1990s indicates a growing contribution of coal combustion and biomass burning to the emissions. The estimated radiative forcing induced by BC and OC impurities in snow has increased since 1980, suggesting an increasing influence of carbonaceous aerosols on the Tibetan glacier melting and the availability of water resources in the surrounding regions. Our study indicates that more attention to OC is merited because of its non-negligible light absorption and the recent rapid increases evident in the ice core record.

  9. Regional modeling of carbonaceous aerosols over Europe-focus on secondary organic aerosols

    International Nuclear Information System (INIS)

    In this study, an improved and complete secondary organic aerosols (SOA) chemistry scheme was implemented in the CHIMERE model. The implementation of isoprene chemistry for SOA significantly improves agreement between long series of simulated and observed particulate matter concentrations. While simulated organic carbon concentrations are clearly improved at elevated sites by adding the SOA scheme, time correlation are impaired at low level sites in Portugal, Italy and Slovakia. At several sites a clear underestimation by the CHIMERE model is noticed in wintertime possibly due to missing wood burning emissions as shown in previous modeling studies. In Europe, the CHIMERE model gives yearly average SOA concentrations ranging from 0.5 μg m-3 in the Northern Europe to 4 μg m-3 over forested regions in Spain, France, Germany and Italy. In addition, our work suggests that during the highest fire emission periods, fires can be the dominant source of primary organic carbon over the Mediterranean Basin, but the SOA contribution from fire emissions is low. Isoprene chemistry has a strong impact on SOA formation when using current available kinetic schemes. (authors)

  10. Origins and composition of fine atmospheric carbonaceous aerosol in the Sierra Nevada Mountains, California

    Directory of Open Access Journals (Sweden)

    D. R. Worton

    2011-06-01

    Full Text Available In this paper we report chemically resolved measurements of organic aerosol (OA and related tracers during the Biosphere Effects on Aerosols and Photochemistry Experiment (BEARPEX at the Blodgett Forest Research Station, California. OA contributed the majority of the mass to the fine atmospheric particles and was predominately oxygenated (OOA. The highest concentrations of OA were during sporadic wildfire influence when aged plumes were impacting the site. In situ measurements of particle phase molecular markers were dominated by secondary compounds and could be categorized into three factors or sources: (1 aged biomass burning emissions and oxidized urban emissions, (2 oxidation products of temperature-driven local biogenic emissions and (3 local light-driven emissions and oxidation products. There were multiple biogenic components that contributed to OA at this site whose contributions varied diurnally, seasonally and in response to changing meteorological conditions, e.g., temperature and precipitation events. Concentrations of isoprene oxidation products were larger when temperatures were higher due to more substantial emissions of isoprene and enhanced photochemistry. Methyl chavicol oxidation contributed similarly to OA during both identified meteorological periods. In contrast, the abundances of monoterpene oxidation products in the particle phase were greater during cooler conditions, even though emissions of the precursors were lower. Following the first precipitation event of the fall the abundances of the monoterpene oxidation products increased dramatically, although the mechanism is not known. OA was correlated with the anthropogenic tracers 2-propyl nitrate and carbon monoxide (CO, consistent with previous observations, while being comprised of mostly non-fossil carbon (>75 %. The correlation between OA and an anthropogenic tracer does not necessarily identify the source of the carbon as being anthropogenic but instead suggests a

  11. Hydrothermal preparation of analogous matrix minerals of CM carbonaceous chondrites from metal alloy particles

    Science.gov (United States)

    Peng, Yiya; Jing, Yunhai

    2014-12-01

    A mineral assemblage that is analogous to the matrix minerals of CM carbonaceous chondrites was produced from an alloyed metal particle mixture of Fe, Mg, Al, Si, and Ni in reducing, basic and S2-containing hydrothermal environments. The elemental ratios of the alloyed metal particle mixture were adopted from reported matrix composition of the carbonaceous chondrite Murchison. The characteristic minerals of the synthetic mineral assemblage are cronstedtite, tochilinite and tochilinite-cronstedtite-intergrowth, other minerals include polyhedral serpentine, chrysotile-like phase, nanotube-like hollow structures, lizardite-like phase, brucite-like phase, etc. (not every mineral appears in a single sample, however, cronstedtite and tochilinite are two invariant minerals in the synthetic mineral assemblage). The dominant individual minerals in the synthetic mineral assemblage have remarkable similarity to the corresponding minerals of the matrix of CM carbonaceous chondrites in composition, morphology, structure, and crystallinity. Our experimental work indicates that matrix minerals of CM carbonaceous chondrites formed billions of years ago may be reproduced under laboratory conditions.

  12. Establishing Global Source-Receptor Relationships for Carbonaceous Aerosol to Characterize Sensitivity of its Climate Forcing to Emission Uncertainties

    Science.gov (United States)

    Wang, H.; Rasch, P. J.; Easter, R. C.; Singh, B.; Qian, Y.; Ma, P.; Zhang, R.

    2013-12-01

    Carbonaceous aerosol (CA) has been identified as an important but very uncertain forcing agent in the Earth's climate system. It has cascading radiative, microphysical and dynamical effects across the different scales in the atmosphere. Light-absorbing CA (e.g., black carbon (BC) and brown carbon) deposited on snow, sea ice and glaciers can accelerate their melting, which can induce more profound impact through positive feedback mechanisms, having important implications for climate change and fresh water availability at the global and regional scale. Many factors can affect the amount and impacts of CA in a specific region such as the Arctic, among which the global distribution of emissions is of primary importance. There are many uncertainties in global CA emissions, which are changing over time. To better understand the response of climate to these uncertainties and to potential future CA emission changes, it is useful to characterize the global source-receptor relationships and attribute CA loading and radiative forcing to various regional and sectoral CA sources. Observational evidence has clearly demonstrated the occurrence of intercontinental long-range transport of aerosols and to some extent the characteristic transport pathways. However, the observational approach alone cannot provide quantitative information on global source-receptor relationships. We have recently improved the treatment of aerosol transport and wet removal processes in the Community Atmosphere Model version 5 (CAM5) and introduced a brute-force aerosol source tagging technique in which aerosol particles emitted from many independent source regions and sectors are tagged and explicitly tracked. We run the CAM5 model in an 'offline' mode (i.e., driven by reanalysis data) so the transport processes are less likely to be subject to model biases in meteorology and circulation patterns. This modeling tool is used to quantify the characteristics (e.g., burden, surface deposition rate, lifetime

  13. Carbonaceous aerosol in an urban and a rural site in the Philippines: Method development and characterization

    International Nuclear Information System (INIS)

    Carbonaceous aerosol, broadly classfied into organic carbon (OC) and elemental carbon (EC), are atmospheric particulates known to have significant effects to health, climate, and visibility. Concentrations of OC and EC in the PM2.5 range were measured for an urban (Valenzuela City, Metro Manila) and a rural (Angat, Bulacan) site in the Philippines from September 2011 to August 2012. The method employed was thermal-optical analysis and the three most widely-recognized protocols, NIOSH, IMPROVEA, and EUSAAR2, were first compared to determine an optical protocol. IMPROVEA with reflectance correction was ultimately selected for the study for its proper OC and EC fractionation and the wide girth of available data for comparison. However, a modified version of the protocol, having an increased OC4 temperature step of 650 degree centegrade from 580 degree centegrade (adopted from the EUSAAR2 protocol) and with transmittance as its correction method, is proposed as optimal for Philippine samples and is predicted to give more accurate results. Measurements show that OC (8.00 ug/m3) and EC 96.63 ug/m3) levels were higher in Valenzuela than in Angat (OC: 4.08 ug/m3, EC: 2.29 ug/m3), as expected. The total contributions of OC and EC to the PM2.5 mass for the urban and rural site were 38.9% and 19.7%, respectively which prove that carbonaceous aerosol constitute a significant part of the fine fraction. Compared to neighboring countries in Asia, the Philippine sites have intermediate OC concentrations (about half of which are from secondary OC formation but greatly elevated EC levels. These results indicate the dominance of highly inefficient combustion sources and highlight the need for the regulation of such emissions. It was found that Valenzuela was dominated by the OC2, OC3, and EC1 fractions which points to gasoline vehicles, the industrial sector, and residential cooking as the possible main sources. Angat, while generally having lower concentrations and being less

  14. Spheroidal carbonaceous particles are a defining stratigraphic marker for the Anthropocene

    OpenAIRE

    Swindles, GT; Watson, E.; Turner, TE; Galloway, JM; Hadlari, T; Wheeler, J; Bacon, KL

    2015-01-01

    There has been recent debate over stratigraphic markers used to demarcate the Anthropocene from the Holocene Epoch. However, many of the proposed markers are found only in limited areas of the world or do not reflect human impacts on the environment. Here we show that spheroidal carbonaceous particles (SCPs), a distinct form of black carbon produced from burning fossil fuels in energy production and heavy industry, provide unambiguous stratigraphic markers of the human activities that have ra...

  15. Positive sampling artifact of carbonaceous aerosols and its influence on the thermal-optical split of OC/EC

    Directory of Open Access Journals (Sweden)

    Y. Cheng

    2009-06-01

    Full Text Available Accurate measurement of carbonaceous aerosols is challenging, due to the sampling artifact and the problems of the split of OC/EC. Two approaches have been used to account for the positive artifact: backup quartz approach in which a backup quartz filter is placed either behind a front quartz filter (QBQ or in a parallel port behind a Teflon filter (QBT, and organic denuder approach in which an organic denuder is placed upstream of the quartz filter. Both approaches were evaluated in Beijing, China, from January to February 2009. 10% of the OC captured by the bare quartz filter was from the positive artifact. The origin of backup OC was quantitatively evaluated by the denuder-based method. All of the QBQ-OC was from gaseous organics passing through the front filter, but the QBQ had not reached equilibrium with gas phase due to the relative small sampling volume resulting in an undercorrection of the positive artifact by 3.7%. QBT-OC was from both gaseous organics passing through the front filter (82% and the evaporated organic carbon (18%, thus overcorrecting the positive artifact by 6.3%. Even the positive artifact-contributed QBT-OC was found to overestimate the positive artifact, perhaps due to the difference in the adsorption properties of the loaded filter and the filter without particle loading. Re-partitioning of PC and EC was performed by the multiple linear regression approach. The attenuation coefficient of PC was twofold higher than that of EC, indicating PC was darker than EC, resulting in the underestimation of native EC by TOT-split-EC. It was also found that PC formed on the bare quartz filter (45.56 m2/g was darker than that formed on the denuded filter (38.64 m2/g, indicating that the underestimation for the bare quartz filter was more significant.

  16. Positive sampling artifact of carbonaceous aerosols and its influence on the thermal-optical split of OC/EC

    Directory of Open Access Journals (Sweden)

    Y. Cheng

    2009-09-01

    Full Text Available Accurate measurement of carbonaceous aerosols is challenging, due to the sampling artifact and the problems of the split of OC/EC. Two approaches have been used to account for the positive artifact: backup quartz approach in which a backup quartz filter is placed either behind a front quartz filter (QBQ or in a parallel port behind a Teflon filter (QBT, and organic denuder approach in which an organic denuder is placed upstream of the quartz filter. Both approaches were evaluated in Beijing, China, from January to February 2009. 10% of the OC captured by the bare quartz filter was from the positive artifact. The origin of backup OC was quantitatively evaluated by the denuder-based method. All of the QBQ OC was from gaseous organics passing through the front filter, but the QBQ had not reached equilibrium with gas phase due to the relative small sampling volume resulting in an undercorrection of the positive artifact by 3.7%. QBT OC was from both gaseous organics passing through the front filter (82% and the evaporated organic carbon (18%, thus overcorrecting the positive artifact by 6.3%. Even the positive artifact-contributed QBT OC was found to overestimate the positive artifact, perhaps due to the difference in the adsorption properties of the loaded filter and the filter without particle loading. Re-partitioning of PC and EC was performed by the multiple linear regression approach. The attenuation coefficient of PC was twofold higher than that of EC, indicating PC was darker than EC, resulting in the underestimation of native EC by TOT-split-EC. It was also found that PC formed on the bare quartz filter (45.56 m2/g was darker than that formed on the denuded filter (38.64 m2/g, indicating that the underestimation for the bare quartz filter was more significant.

  17. Origins and composition of fine atmospheric carbonaceous aerosol in the Sierra Nevada Mountains, California

    Directory of Open Access Journals (Sweden)

    D. R. Worton

    2011-10-01

    Full Text Available In this paper we report chemically resolved measurements of organic aerosol (OA and related tracers during the Biosphere Effects on Aerosols and Photochemistry Experiment (BEARPEX at the Blodgett Forest Research Station, California from 15 August–10 October 2007. OA contributed the majority of the mass to the fine atmospheric particles and was predominately oxygenated (OOA. The highest concentrations of OA were during sporadic wildfire influence when aged plumes were impacting the site. In situ measurements of particle phase molecular markers were dominated by secondary compounds and along with gas phase compounds could be categorized into six factors or sources: (1 aged biomass burning emissions and oxidized urban emissions, (2 oxidized urban emissions (3 oxidation products of monoterpene emissions, (4 monoterpene emissions, (5 anthropogenic emissions and (6 local methyl chavicol emissions and oxidation products. There were multiple biogenic components that contributed to OA at this site whose contributions varied diurnally, seasonally and in response to changing meteorological conditions, e.g. temperature and precipitation events. Concentrations of isoprene oxidation products were larger when temperatures were higher during the first half of the campaign (15 August–12 September due to more substantial emissions of isoprene and enhanced photochemistry. The oxidation of methyl chavicol, an oxygenated terpene emitted by ponderosa pine trees, contributed similarly to OA throughout the campaign. In contrast, the abundances of monoterpene oxidation products in the particle phase were greater during the cooler conditions in the latter half of the campaign (13 September–10 October, even though emissions of the precursors were lower, although the mechanism is not known. OA was correlated with the anthropogenic tracers 2-propyl nitrate and carbon monoxide (CO, consistent with previous observations, while being comprised of mostly non-fossil carbon

  18. Origins and composition of fine atmospheric carbonaceous aerosol in the Sierra Nevada Mountains, California

    Science.gov (United States)

    Worton, D. R.; Goldstein, A. H.; Farmer, D. K.; Docherty, K. S.; Jimenez, J. L.; Gilman, J. B.; Kuster, W. C.; de Gouw, J.; Williams, B. J.; Kreisberg, N. M.; Hering, S. V.; Bench, G.; McKay, M.; Kristensen, K.; Glasius, M.; Surratt, J. D.; Seinfeld, J. H.

    2011-10-01

    In this paper we report chemically resolved measurements of organic aerosol (OA) and related tracers during the Biosphere Effects on Aerosols and Photochemistry Experiment (BEARPEX) at the Blodgett Forest Research Station, California from 15 August-10 October 2007. OA contributed the majority of the mass to the fine atmospheric particles and was predominately oxygenated (OOA). The highest concentrations of OA were during sporadic wildfire influence when aged plumes were impacting the site. In situ measurements of particle phase molecular markers were dominated by secondary compounds and along with gas phase compounds could be categorized into six factors or sources: (1) aged biomass burning emissions and oxidized urban emissions, (2) oxidized urban emissions (3) oxidation products of monoterpene emissions, (4) monoterpene emissions, (5) anthropogenic emissions and (6) local methyl chavicol emissions and oxidation products. There were multiple biogenic components that contributed to OA at this site whose contributions varied diurnally, seasonally and in response to changing meteorological conditions, e.g. temperature and precipitation events. Concentrations of isoprene oxidation products were larger when temperatures were higher during the first half of the campaign (15 August-12 September) due to more substantial emissions of isoprene and enhanced photochemistry. The oxidation of methyl chavicol, an oxygenated terpene emitted by ponderosa pine trees, contributed similarly to OA throughout the campaign. In contrast, the abundances of monoterpene oxidation products in the particle phase were greater during the cooler conditions in the latter half of the campaign (13 September-10 October), even though emissions of the precursors were lower, although the mechanism is not known. OA was correlated with the anthropogenic tracers 2-propyl nitrate and carbon monoxide (CO), consistent with previous observations, while being comprised of mostly non-fossil carbon (>75%). The

  19. Pyrolysis of carbonaceous particles and properties of Carbonaceous-g-Poly (acrylic acid-co-acrylamide superabsorbent polymer for agricultural applications

    Directory of Open Access Journals (Sweden)

    Ghazali S.

    2016-01-01

    Full Text Available Utilisation of fertilizer and water are very important in determining the production of agriculture nowadays. The excessive use of fertilizer in plantation somehow could leads to environmental pollution. The present study reported a synthesis of controlled release water retention (CRWR fertilizer coating with superabsorbent polymer (SAPs. Superabsorbent polymer (SAPs are polymers that have ability to absorb and retain large amounts of water relative to their own mass. The presence of coating layer of SAPs on fertilizer granules was believed could reduce excessive used of fertilizer by controlling their dissolution rates and also reduce the environmental pollution. In this study, the effect on the addition of carbonaceous filler in SAPs on the water absorbency was also be compared with control SAPs (without carbonaceous particles. In this study, the carbonaceous filler were obtained from pyrolysis process of empty fruit bunch (EFB biomass. The synthesized of SAPs and carbonaceous-SAPs were carried out via solution polymerization technique by using monomer of poly(acrylic acid (AA, acrylamide (AM, cross linker, methylene bisacrylamide (MBA and initiator, ammonium peroxodisulfate (APS that partially neutralized with sodium hydroxide (NaOH. The CRWR fertilizer was later be prepared by coated the fertilizer granule with SAPs and carbonaceous-SAPs. The water absorbency, morphology and the bonding formation of both CRWR fertilizer were investigated by using tea-beg method, Scanning Electron Microscopy (SEM and Fourier Transform Infrared Spectrophotometer (FTIR, respectively. Moreover, the water retention studies was conducted in order to investigate the efficiency of CRWR coated with SAP and carbonaceous-SAP in retaining the water content in different soil (organic and top soil. Based on the results, the CRWR fertilizer that was coated with carbonaceous-SAP had higher water absorbency value than the CRWR fertilizer without carbonaceous-SAP. Meanwhile

  20. Holographic interferometry for aerosol particle characterization

    International Nuclear Information System (INIS)

    Using simulations based on Mie theory, this work shows how double-exposure digital holography can be used to measure the change in size of an expanding, or contracting, spherical particle. Here, a single particle is illuminated by a plane wave twice during its expansion: once when the particle is 27λ in radius, and again when it is 47λ. A hologram is formed from each illumination stage from the interference of the scattered and unscattered, i.e., incident, light. The two holograms are then superposed to form a double exposure. By applying the Fresnel–Kirchhoff diffraction theory to the double-exposed hologram, a silhouette-like image of the particle is computationally reconstructed that is superposed with interference fringes. These fringes are a direct result of the change in particle size occurring between the two illumination stages. The study finds that expansion on the scale of ∼6λ is readily discerned from the reconstructed particle image. This work could be important for improved characterization of single and multiple aerosol particles in situ. For example, by illuminating an aerosol particle with infrared light, it may be possible to measure photothermally induced particle expansion, thus providing insight into a particle's material properties simultaneous with an image of the particle. - Highlights: • A computational model to simulate digital holography is developed. • The model is used to image a multi-wavelength sized, expanding spherical particle. • An interferometry technique is described that can measure the particle expansion. • Implications for laboratory-based aerosol particle characterization are described

  1. Variability of carbonaceous aerosols in remote, rural, urban and industrial environments in Spain: implications for air quality policy

    Directory of Open Access Journals (Sweden)

    X. Querol

    2013-03-01

    Full Text Available We interpret here the variability of levels of carbonaceous aerosols based on a 12-yr database from 78 monitoring stations across Spain especially compiled for this article. Data did not evidence any spatial trends of carbonaceous aerosols across the country. Conversely, results show marked differences in average concentrations from the cleanest, most remote sites (around 1 μg m−3 of non-mineral carbon (nmC, mostly made of organic carbon (OC, with very little elemental carbon (EC 0.1 μg m−3; OC/EC = 12–15, to the highly polluted major cities (8–10 μg m−3 of nmC; 3–4 μg m−3 of EC; 4–5 μg m−3 of OC; OC/EC = 1–2. Thus, urban (and very specific industrial pollution was found to markedly increase levels of carbonaceous aerosols in Spain, with much lower impact of biomass burning. Correlations between yearly averaged OC/EC and EC concentrations adjust very well to a potential equation (OC/EC = 3.37 EC−0.67 R2 = 0.94. A similar equation is obtained when including average concentrations obtained at other European sites (y = 3.61x−0.5, R2 = 0.78. A clear seasonal variability in OC and EC concentrations was detected. Both OC and EC concentrations were higher during winter at the traffic and urban sites, but OC increased during the warmer months at the rural sites. Hourly equivalent black carbon (EBC concentrations at urban sites accurately depict road traffic contributions, varying with distance to road, traffic volume and density, mixing layer height and wind speed. Weekday urban rush-hour EBC peaks are mimicked by concentrations of primary gaseous emissions from road traffic, whereas a single midday peak is characteristic of remote and rural sites. Decreasing annual trends for carbonaceous aerosols were observed between 1999 and 2011 at a large number of stations, probably reflecting the impact of the EURO4 and EURO5 standards in reducing the diesel PM emissions. This has resulted in some cases in an increasing trend of NO2

  2. Sulfur dioxide and primary carbonaceous aerosol emissions in China and India, 1996–2010

    Directory of Open Access Journals (Sweden)

    Z. Lu

    2011-09-01

    Full Text Available China and India are the two largest anthropogenic aerosol generating countries in the world. In this study, we develop a new inventory of sulfur dioxide (SO2 and primary carbonaceous aerosol (i.e., black and organic carbon, BC and OC emissions from these two countries for the period 1996–2010, using a technology-based methodology. Emissions from major anthropogenic sources and open biomass burning are included, and time-dependent trends in activity rates and emission factors are incorporated in the calculation. Year-specific monthly temporal distributions for major sectors and gridded emissions at a resolution of 0.1°×0.1° distributed by multiple year-by-year spatial proxies are also developed. In China, the interaction between economic development and environmental protection causes large temporal variations in the emission trends. From 1996 to 2000, emissions of all three species showed a decreasing trend (by 9 %–17 % due to a slowdown in economic growth, a decline in coal use in non-power sectors, and the implementation of air pollution control measures. With the economic boom after 2000, emissions from China changed dramatically. BC and OC emissions increased by 46 % and 33 % to 1.85 Tg and 4.03 Tg in 2010. SO2 emissions first increased by 61 % to 34.0 Tg in 2006, and then decreased by 9.2 % to 30.8 Tg in 2010 due to the wide application of flue-gas desulfurization (FGD equipment in power plants. Driven by the remarkable energy consumption growth and relatively lax emission controls, emissions from India increased by 70 %, 41 %, and 35 % to 8.81 Tg, 1.02 Tg, and 2.74 Tg in 2010 for SO2, BC, and OC, respectively. Monte Carlo simulations are used to quantify the emission uncertainties. The average 95 % confidence intervals (CIs of SO2, BC, and OC emissions are estimated to be −16 %–17 %, −43 %–93 %, and −43 %–80 % for China, and −15 %–16 %, −41 %–87 %, and −44 %–92

  3. Sulfur dioxide and primary carbonaceous aerosol emissions in China and India, 1996–2010

    Directory of Open Access Journals (Sweden)

    Z. Lu

    2011-07-01

    Full Text Available China and India are the two largest anthropogenic aerosol generating countries in the world. In this study, we develop a new inventory of sulfur dioxide (SO2 and primary carbonaceous aerosol (i.e., black and organic carbon, BC and OC emissions from these two countries for the period 1996–2010, using a technology-based methodology. Emissions from major anthropogenic sources and open biomass burning are included, and time-dependent trends in activity rates and emission factors are incorporated in the calculation. Year-specific monthly fractions for major sectors and gridded emissions at a resolution of 0.1° × 0.1° distributed by multiple year-by-year spatial proxies are also developed. In China, the interaction between economic development and environmental protection causes large temporal variations in the emission trends. From 1996 to 2000, emissions of all three species showed a decreasing trend (by 9 %–17 % due to a slowdown in economic growth, a decline in coal use in non-power sectors, and the implementation of air pollution control measures. With the economic boom after 2000, emissions from China changed dramatically. BC and OC emissions increased by 46 % and 33 % to 1.85 Tg and 4.03 Tg in 2010. SO2 emissions first increased by 61 % to 34.0 Tg in 2006, and then decreased by 9.2 % to 30.8 Tg in 2010 due to the wide application of flue-gas desulfurization (FGD equipment in power plants. Driven by the remarkable energy consumption growth and relatively lax emission controls, emissions from India increased by 70 %, 41 %, and 35 % to 8.81 Tg, 1.02 Tg, and 2.74 Tg in 2010 for SO2, BC, and OC, respectively. Monte Carlo simulations are used to quantify the emission uncertainties. The average 95 % confidence intervals (CIs of SO2, BC, and OC emissions are estimated to be −16 %–17 %, −43 %–93 %, and −43 %–80 % for China, and −15 %–16 %, −41 %–87 %, and −44 %–92 % for India

  4. Holographic interferometry for aerosol particle characterization

    Science.gov (United States)

    Berg, Matthew J.; Subedi, Nava R.

    2015-01-01

    Using simulations based on Mie theory, this work shows how double-exposure digital holography can be used to measure the change in size of an expanding, or contracting, spherical particle. Here, a single particle is illuminated by a plane wave twice during its expansion: once when the particle is 27 λ in radius, and again when it is 47 λ. A hologram is formed from each illumination stage from the interference of the scattered and unscattered, i.e., incident, light. The two holograms are then superposed to form a double exposure. By applying the Fresnel-Kirchhoff diffraction theory to the double-exposed hologram, a silhouette-like image of the particle is computationally reconstructed that is superposed with interference fringes. These fringes are a direct result of the change in particle size occurring between the two illumination stages. The study finds that expansion on the scale of ~ 6 λ is readily discerned from the reconstructed particle image. This work could be important for improved characterization of single and multiple aerosol particles in situ. For example, by illuminating an aerosol particle with infrared light, it may be possible to measure photothermally induced particle expansion, thus providing insight into a particle's material properties simultaneous with an image of the particle.

  5. Characterization of emissions from South Asian biofuels and application to source apportionment of carbonaceous aerosol in the Himalayas

    Science.gov (United States)

    Stone, Elizabeth A.; Schauer, James J.; Pradhan, Bidya Banmali; Dangol, Pradeep Man; Habib, Gazala; Venkataraman, Chandra; Ramanathan, V.

    2010-03-01

    This study focuses on improving source apportionment of carbonaceous aerosol in South Asia and consists of three parts: (1) development of novel molecular marker-based profiles for real-world biofuel combustion, (2) application of these profiles to a year-long data set, and (3) evaluation of profiles by an in-depth sensitivity analysis. Emissions profiles for biomass fuels were developed through source testing of a residential stove commonly used in South Asia. Wood fuels were combusted at high and low rates, which corresponded to source profiles high in organic carbon (OC) or high in elemental carbon (EC), respectively. Crop wastes common to the region, including rice straw, mustard stalk, jute stalk, soybean stalk, and animal residue burnings, were also characterized. Biofuel profiles were used in a source apportionment study of OC and EC in Godavari, Nepal. This site is located in the foothills of the Himalayas and was selected for its well-mixed and regionally impacted air masses. At Godavari, daily samples of fine particulate matter (PM2.5) were collected throughout the year of 2006, and the annual trends in particulate mass, OC, and EC followed the occurrence of a regional haze in South Asia. Maximum concentrations occurred during the dry winter season and minimum concentrations occurred during the summer monsoon season. Specific organic compounds unique to aerosol sources, molecular markers, were measured in monthly composite samples. These markers implicated motor vehicles, coal combustion, biomass burning, cow dung burning, vegetative detritus, and secondary organic aerosol as sources of carbonaceous aerosol. A molecular marker-based chemical mass balance (CMB) model provided a quantitative assessment of primary source contributions to carbonaceous aerosol. The new profiles were compared to widely used biomass burning profiles from the literature in a sensitivity analysis. This analysis indicated a high degree of stability in estimates of source

  6. Simulating the formation of carbonaceous aerosol in a European Megacity (Paris) during the MEGAPOLI summer and winter campaigns

    Science.gov (United States)

    Fountoukis, Christos; Megaritis, Athanasios G.; Skyllakou, Ksakousti; Charalampidis, Panagiotis E.; Denier van der Gon, Hugo A. C.; Crippa, Monica; Prévôt, André S. H.; Fachinger, Friederike; Wiedensohler, Alfred; Pilinis, Christodoulos; Pandis, Spyros N.

    2016-03-01

    We use a three-dimensional regional chemical transport model (PMCAMx) with high grid resolution and high-resolution emissions (4 × 4 km2) over the Paris greater area to simulate the formation of carbonaceous aerosol during a summer (July 2009) and a winter (January/February 2010) period as part of the MEGAPOLI (megacities: emissions, urban, regional, and global atmospheric pollution and climate effects, and Integrated tools for assessment and mitigation) campaigns. Model predictions of carbonaceous aerosol are compared against Aerodyne aerosol mass spectrometer and black carbon (BC) high time resolution measurements from three ground sites. PMCAMx predicts BC concentrations reasonably well reproducing the majority (70 %) of the hourly data within a factor of two during both periods. The agreement for the summertime secondary organic aerosol (OA) concentrations is also encouraging (mean bias = 0.1 µg m-3) during a photochemically intense period. The model tends to underpredict the summertime primary OA concentrations in the Paris greater area (by approximately 0.8 µg m-3) mainly due to missing primary OA emissions from cooking activities. The total cooking emissions are estimated to be approximately 80 mg d-1 per capita and have a distinct diurnal profile in which 50 % of the daily cooking OA is emitted during lunch time (12:00-14:00 LT) and 20 % during dinner time (20:00-22:00 LT). Results also show a large underestimation of secondary OA in the Paris greater area during wintertime (mean bias = -2.3 µg m-3) pointing towards a secondary OA formation process during low photochemical activity periods that is not simulated in the model.

  7. Carbonaceous aerosols in China: top-down constraints on primary sources and estimation of secondary contribution

    Directory of Open Access Journals (Sweden)

    T.-M. Fu

    2012-03-01

    Full Text Available We simulated elemental carbon (EC and organic carbon (OC aerosols in China and compared model results to surface measurements at Chinese rural and background sites, with the goal of deriving "top-down" emission estimates of EC and OC, as well as better quantifying the secondary sources of OC. We included in the model state-of-the-science Chinese "bottom-up" emission inventories for EC (1.92 TgC yr−1 and OC (3.95 TgC yr−1, as well as updated secondary OC formation pathways. The average simulated annual mean EC concentration at rural and background sites was 1.1 μgC m−3, 56% lower than the observed 2.5 μgC m−3. The average simulated annual mean OC concentration at rural and background sites was 3.4 μgC m−3, 76% lower than the observed 14 μgC m−3. Multiple regression to fit surface monthly mean EC observations at rural and background sites yielded the best estimate of Chinese EC source of 3.05 ± 0.78 TgC yr−1. Based on the top-down EC emission estimate and observed seasonal primary OC/EC ratios, we estimated Chinese OC emissions to be 6.67 ± 1.30 TgC yr−1. Using these top-down estimates, the simulated average annual mean EC concentration at rural and background sites was significantly improved to 1.9 μgC m−3. However, the model still significantly underestimated observed OC in all seasons (simulated average annual mean OC at rural and background sites was 5.4 μgC m−3, with little skill in capturing the spatiotemporal variability. Secondary formation accounts for 21% of Chinese annual mean surface OC in the model, with isoprene being the most important precursor. In summer, as high as 62% of the observed surface OC may be due to secondary formation in eastern China. Our analysis points to four shortcomings in the current bottom-up inventories of Chinese carbonaceous aerosols: (1 the anthropogenic source is

  8. Carbonaceous aerosols in China: top-down constraints on primary sources and estimation of secondary contribution

    Directory of Open Access Journals (Sweden)

    T.-M. Fu

    2011-10-01

    Full Text Available We simulate elemental carbon (EC and organic carbon (OC aerosols in China and compare model results to surface measurements at Chinese rural and background sites, with the goal of deriving "top-down" emission estimates of EC and OC, as well as better quantifying the secondary sources of OC. We include in the model state-of-the-science Chinese "bottom-up" emission inventories for EC (1.92 Tg C yr−1 and OC (3.95 Tg C yr−1, as well as updated secondary OC formation pathways. The average simulated annual mean EC concentration at rural and background site is 1.1 μg C m−3, 56% lower than the observed 2.5 μg C m−3. The average simulated annual mean OC concentration at rural and background sites is 3.4 μg C m−3, 76% lower than the observed 14 μg C m−3. Multiple regression to fit surface monthly mean EC observations at rural and background sites yields best estimate of Chinese EC source of 3.05 ± 0.78 Tg C yr−1. Based on the top-down EC emission estimate and observed seasonal primary OC/EC ratios, we estimate Chinese OC total emissions to be 6.67 ± 1.30 Tg C yr−1. Using these top-down estimates, the simulated average annual mean EC concentration at rural and background sites significantly improved to 1.9 μg C m−3. However, the model still significantly underestimates observed OC in all seasons (simulated average annual mean OC at rural and background sites is 5.4 μg C m−3, with little skill in capturing the spatiotemporal variability. Secondary formation accounts for 21% of Chinese annual mean surface OC in the model, with isoprene being the most important precursor. In summer, as high as 62% of the observed surface OC may be due to secondary formation in eastern China. Our analysis points to three shortcomings in the current bottom-up inventories of Chinese carbonaceous aerosols: (1 the anthropogenic source is

  9. On the isolation of OC and EC and the optimal strategy of radiocarbon-based source apportionment of carbonaceous aerosols

    Directory of Open Access Journals (Sweden)

    Y. L. Zhang

    2012-07-01

    Full Text Available Radiocarbon (14C measurements of elemental carbon (EC and organic carbon (OC separately (as opposed to only total carbon, TC allow an unambiguous quantification of their non-fossil and fossil sources and represent an improvement in carbonaceous aerosol source apportionment. Isolation of OC and EC for accurate 14C determination requires complete removal of interfering fractions with maximum recovery. To evaluate the extent of positive and negative artefacts during OC and EC separation, we performed sample preparation with a commercial Thermo-Optical OC/EC Analyser (TOA by monitoring the optical properties of the sample during the thermal treatments. Extensive attention has been devoted to the set-up of TOA conditions, in particular, heating program and choice of carrier gas. Based on different types of carbonaceous aerosols samples, an optimised TOA protocol (Swiss_4S with four steps is developed to minimise the charring of OC, the premature combustion of EC and thus artefacts of 14C-based source apportionment of EC. For the isolation of EC for 14C analysis, the water-extraction treatment on the filter prior to any thermal treatment is an essential prerequisite for subsequent radiocarbon; otherwise the non-fossil contribution may be overestimated due to the positive bias from charring. The Swiss_4S protocol involves the following consecutive four steps (S1, S2, S3 and S4: (1 S1 in pure oxygen (O2 at 375 °C for separation of OC for untreated filters, and water-insoluble organic carbon (WINSOC for water-extracted filters; (2 S2 in O2 at 475 °C, followed by (3 S3 in helium (He at 650 °C, aiming at complete OC removal before EC isolation and leading to better consistency with thermal-optical protocols like EUSAAR_2, compared to pure oxygen methods; and (4 S4 in O2 at 760 °C for recovery of the remaining EC.

    WINSOC was found to have a significantly higher fossil

  10. On the isolation of OC and EC and the optimal strategy of radiocarbon-based source apportionment of carbonaceous aerosols

    Directory of Open Access Journals (Sweden)

    Y. L. Zhang

    2012-11-01

    Full Text Available Radiocarbon (14C measurements of elemental carbon (EC and organic carbon (OC separately (as opposed to only total carbon, TC allow an unambiguous quantification of their non-fossil and fossil sources and represent an improvement in carbonaceous aerosol source apportionment. Isolation of OC and EC for accurate 14C determination requires complete removal of interfering fractions with maximum recovery. The optimal strategy for 14C-based source apportionment of carbonaceous aerosols should follow an approach to subdivide TC into different carbonaceous aerosol fractions for individual 14C analyses, as these fractions may differ in their origins. To evaluate the extent of positive and negative artefacts during OC and EC separation, we performed sample preparation with a commercial Thermo-Optical OC/EC Analyser (TOA by monitoring the optical properties of the sample during the thermal treatments. Extensive attention has been devoted to the set-up of TOA conditions, in particular, heating program and choice of carrier gas. Based on different types of carbonaceous aerosols samples, an optimised TOA protocol (Swiss_4S with four steps is developed to minimise the charring of OC, the premature combustion of EC and thus artefacts of 14C-based source apportionment of EC. For the isolation of EC for 14C analysis, the water-extraction treatment on the filter prior to any thermal treatment is an essential prerequisite for subsequent radiocarbon measurements; otherwise the non-fossil contribution may be overestimated due to the positive bias from charring. The Swiss_4S protocol involves the following consecutive four steps (S1, S2, S3 and S4: (1 S1 in pure oxygen (O2 at 375 °C for separation of OC for untreated filters and water-insoluble organic carbon (WINSOC for water-extracted filters; (2 S2 in O2 at 475 °C followed by (3 S3 in helium (He at 650 °C, aiming at complete

  11. Characteristics of carbonaceous aerosol in a two-week campaign at Ny-(A)lesund

    Institute of Scientific and Technical Information of China (English)

    2005-01-01

    The concentrations of organic carbon (OC) and elemental carbon (EC)in total suspended particle (TSP) were investigated at Ny-(A)lesund, Svalbard in a two-week campaign. The levels of OC and EC are 0.86 ±0.27 μgm-3 (mean±standard deviation) and 0. 19±0.10 μgm-3 , respectively. Back trajectory analysis of air masses arriving at Ny-(A)lesund reveals that long-range transport of polluted air play insignificant role in OC and EC levels, to which the potential influence of the local contamination were ascribed. The average OC/EC ratio is 5.41,suggesting the presence of the secondary organic aerosols. The estimated secondary organic carbon (SOC) in TSP is 0.59 μg/m3 , accounting for 64% of the total organic carbon.

  12. Nuclear track radiography of 'hot' aerosol particles

    CERN Document Server

    Boulyga, S F; Kievets, M K; Lomonosova, E M; Zhuk, I V; Yaroshevich, O I; Perelygin, V P; Petrova, R I; Brandt, R; Vater, P

    1999-01-01

    Nuclear track radiography was applied to identify aerosol 'hot' particles which contain elements of nuclear fuel and fallout after Chernobyl NPP accident. For the determination of the content of transuranium elements in radioactive aerosols the measurement of the alpha-activity of 'hot' particles by SSNTD was used in this work, as well as radiography of fission fragments formed as a result of the reactions (n,f) and (gamma,f) in the irradiation of aerosol filters by thermal neutrons and high energy gamma quanta. The technique allowed the sizes and alpha-activity of 'hot' particles to be determined without extracting them from the filter, as well as the determination of the uranium content and its enrichment by sup 2 sup 3 sup 5 U, sup 2 sup 3 sup 9 Pu and sup 2 sup 4 sup 1 Pu isotopes. Sensitivity of determination of alpha activity by fission method is 5x10 sup - sup 6 Bq per particle. The software for the system of image analysis was created. It ensured the identification of track clusters on an optical imag...

  13. Condensation on Aerosol Particles and its Inhibition.

    Science.gov (United States)

    Liu, Peter Shen King

    The atmospheric aerosol is of primary importance in the formation of precipitation. Except in the neighbourhood of large sources of pollution most of the atmospheric particles are of natural origin, but human contribution is increasing at such a rate that within a comparatively short time it may equal nature's. Such an increase in the atmospheric particulate load may have significant effects on the distribution and intensity of precipitation. There is a general perception that most of the atmospheric particulate load is soluble in water or has some soluble component and soluble particles condense water more readily than insoluble. In this work a study is made of the solubility of the atmospheric aerosol at various relative humidities. The results confirm that much of the atmospheric aerosol is indeed soluble, but that the soluble proportion is highly variable. This result has significant implications for studies of air pollution in which the respirable fraction of the atmospheric aerosol is deduced from the results of long term dichotomous sampling. Results are also presented of studies in which an attempt was made to inhibit the condensation of water on man-made and adventitious particles with a view to modifying their possible climatic effects. This work has demonstrated that certain agents, notably long chain amines, do indeed have an inhibiting effect on the condensation of water on particles which have been exposed to them, but that the effect of the agents so far tested is not sufficiently great to be of immediate practical importance. It is concluded that further advances must await more precise methods of producing small supersaturations reliably and reproducibly.

  14. Contribution of brown carbon and lensing to the direct radiative effect of carbonaceous aerosols from biomass and biofuel burning emissions

    Science.gov (United States)

    Saleh, Rawad; Marks, Marguerite; Heo, Jinhyok; Adams, Peter J.; Donahue, Neil M.; Robinson, Allen L.

    2015-10-01

    We present global direct radiative effect (DRE) calculations of carbonaceous aerosols emitted from biomass/biofuel burning addressing the interplay between two poorly constrained contributions to DRE: mixing state of black carbon (lensing) and light absorption by organic aerosol (OA) due to the presence of brown carbon (BrC). We use the parameterization of Saleh et al. (2014) which captures the variability in biomass/biofuel OA absorption. The global mean effect of OA absorption is +0.22 W/m2 and +0.12 W/m2 for externally and internally mixed cases, while the effect of lensing is +0.39 W/m2 and +0.29 W/m2 for nonabsorbing and absorbing OA cases, signifying the nonlinear interplay between OA absorption and lensing. These two effects can be overestimated if not treated simultaneously in radiative transfer calculations. The combined effect of OA absorption and lensing increases the global mean DRE of biomass/biofuel aerosols from -0.46 W/m2 to +0.05 W/m2 and appears to reduce the gap between existing model-based and observationally constrained DRE estimates. We observed a strong sensitivity to these parameters in key regions, where DRE shifts from strongly negative ( +1 W/m2) when accounting for lensing and OA absorption.

  15. Laboratory Studies of Processing of Carbonaceous Aerosols by Atmospheric Oxidants/Hygroscopicity and CCN Activity of Secondary & Processed Primary Organic Aerosols

    Energy Technology Data Exchange (ETDEWEB)

    Ziemann, P.J.; Arey, J.; Atkinson, R.; Kreidenweis, S.M.; Petters, M.D.

    2012-06-13

    The atmosphere is composed of a complex mixture of gases and suspended microscopic aerosol particles. The ability of these particles to take up water (hygroscopicity) and to act as nuclei for cloud droplet formation significantly impacts aerosol light scattering and absorption, and cloud formation, thereby influencing air quality, visibility, and climate in important ways. A substantial, yet poorly characterized component of the atmospheric aerosol is organic matter. Its major sources are direct emissions from combustion processes, which are referred to as primary organic aerosol (POA), or in situ processes in which volatile organic compounds (VOCs) are oxidized in the atmosphere to low volatility reaction products that subsequent condense to form particles that are referred to as secondary organic aerosol (SOA). POA and VOCs are emitted to the atmosphere from both anthropogenic and natural (biogenic) sources. The overall goal of this experimental research project was to conduct laboratory studies under simulated atmospheric conditions to investigate the effects of the chemical composition of organic aerosol particles on their hygroscopicity and cloud condensation nucleation (CCN) activity, in order to develop quantitative relationships that could be used to more accurately incorporate aerosol-cloud interactions into regional and global atmospheric models. More specifically, the project aimed to determine the products, mechanisms, and rates of chemical reactions involved in the processing of organic aerosol particles by atmospheric oxidants and to investigate the relationships between the chemical composition of organic particles (as represented by molecule sizes and the specific functional groups that are present) and the hygroscopicity and CCN activity of oxidized POA and SOA formed from the oxidation of the major classes of anthropogenic and biogenic VOCs that are emitted to the atmosphere, as well as model hydrocarbons. The general approach for this project was

  16. Impacts of controlling biomass burning emissions on wintertime carbonaceous aerosol in Europe

    NARCIS (Netherlands)

    Fountoukis, C.; Butler, T.; Lawrence, M.G.; Denier van der Gon, H.A.C.; Visschedijk, A.J.H.; Charalampidis, P.; Pilinis, C.; Pandis, S.N.

    2014-01-01

    We use a 3-D regional chemical transport model, with the latest advancements in the organic aerosol (OA) treatment, and an updated emission inventory for wood combustion to study the organic aerosol change in response to the replacement of current residential wood combustion technologies with pellet

  17. The study on differentiated particle size sampling technology of aerosols

    International Nuclear Information System (INIS)

    This article introduces basic principle of differentiated particle size sampling technology of aerosols. This sampling technology is used to conduct a experimental research on the aerosols particles size distribution of uranium and radon and it's daughters. Experimental results showed that the part of radon and it's daughters aerosols particles size smaller than 0.43 μm reached 76.4%. The part of radon and it's daughters aerosols particles size less than 1 μm reached 96.3%. The part of uranium aerosol particles size larger than 4.7 μm under specific conditions is 94%, the part of aerosol particles size larger than 10 μm is 72%. According to the experiment's result, we designed a new sampling equipments that cutting size is 1 μm to collect samples of aerosols, and it is used in the separation efficiency experiments of 241Am aerosols. Experimental results showed that the separation efficiency of 241Am aerosols can reach 94.2%. Thus, using the differentiated particle size sampling technology to collect samples of plutonium aerosols, in the sampling process can reduce the effect of natural background aerosols. (authors)

  18. Inorganic markers, carbonaceous components and stable carbon isotope from biomass burning aerosols in northeast China

    Science.gov (United States)

    Cao, F.; Zhang, Y.; Kawamura, K.

    2015-12-01

    To better characterize the sources of fine particulate matter (i.e. PM2.5) in Sanjiang Plain, Northeast China, aerosol chemical composition such total carbon (TC), organic carbon (OC), elemental carbon (EC), water-soluble organic carbon (WSOC), and inorganic ions were studied as well as stable carbon isotopic composition (δ13C) of TC. Intensively open biomass burning episodes were identified from late September to early October by satellite fire and aerosol optical depth maps. During the biomass burning episodes, concentrations of PM2.5, OC, EC, and WSOC increased by a factor of 4-12 compared to non-biomass-burning periods. Non-sea-salt potassium is strongly correlated with PM2.5, OC, EC and WSOC, suggesting an important contribution of biomass burning emission. The enrichment in both the non-sea-salt potassium and chlorine is significantly larger than other inorganic species, indicating that biomass burning aerosols in Sanjiang Plain is mostly fresh and less aged. In addition, WSOC to OC ratio is relatively lower compared to that reported in biomass burning aerosols in tropical regions, supporting that biomass burning aerosols in Sanjiang Plain is mostly primary and secondary organic aerosols is not significant. A lower average δ13C value (-26.2‰) is found for the biomass-burning aerosols, suggesting a dominant contribution from combustion of C3 plants in the studied region.

  19. 碳同位素技术在碳质气溶胶源解析中应用的研究进展%The Use of Carbon Isotope Analysis in Source Apportionment of Carbonaceous Aerosols: A Review

    Institute of Scientific and Technical Information of China (English)

    张世春; 王毅勇; 童全松

    2013-01-01

    概述了国内外14C和13C技术在大气碳质气溶胶源解析中应用的研究进展,指出14C在碳质气溶胶源解析研究中具有不可替代的独特优势,联合采用14C和13C技术有利于解决多种排放源的区分问题;随着碳质气溶胶组分分离技术的进步,对有机碳(0C)和黑碳(BC)等组分中14C的研究获得重要进展;除需深入研究13C的分馏机制外,建立各种排放源在不同区域的δ13C值域“特征谱”的重要性也日益突出;结合14C和13C以外的其他示踪剂、模型和分析方法将提供更多关于气溶胶来源的信息,并减小来源贡献率估算的不确定性.%The observation and source apportionment of carbonaceous aerosols is one of the focus of studies in the current scientific community. Radioactive (14C) and stable (13C) carbon isotopes have become useful tools in the source apportionment studies for carbonaceous aerosols. In this paper, we review the recent development of carbon isotope techniques, and explore its potential to be used for source apportionment for carbonaceous aerosols. It was pointed out that 14C has unique advantages in the quantitative distinguishment between fossil fuel and contemporary biomass combustion sources of atmospheric Organic Carbon (0C) and Black Carbon ( BC) , and that the combined C- C analysis can better constrain the sources of carbonaceous aerosols. Recent progress towards isolating OC and BC from other components of the particles has made it appicable to perform C measurements for OC and BC seperately. As for 13C, it was proposed that while it is very important to investigate the isotopic fraetionation mechanism of δ13C values of the carbonaceous aerosols, a regional δ13C signature map for the carbonacoues aerosols should be biult up aiming to facilitate explaining the δ13C variations and hence constraining the emisson sources. Future research that uses these carbon isotope techniques, in conjunction with other means such as

  20. Characteristics and major sources of carbonaceous aerosols in PM2.5 from Sanya, China

    International Nuclear Information System (INIS)

    PM2.5 samples were collected in Sanya, China in summer and winter in 2012/2013. Organic carbon (OC), elemental carbon (EC), and non-polar organic compounds including n-alkanes (n-C14-n-C40) and polycyclic aromatic hydrocarbons (PAHs) were quantified. The concentrations of these carbonaceous matters were generally higher in winter than summer. The estimated secondary organic carbon (OCsec) accounted for 38% and 54% of the total organic carbon (TOC) in winter and summer, respectively. The higher value of OCsec in addition to the presences of photochemically-produced PAHs in summer supports that photochemical conversions of organics are much active at the higher air temperatures and with stronger intense solar radiation. Carbon preference index (CPI) and percent contribution of wax n-alkanes suggest that anthropogenic sources were more dominant than derivation from terrestrial plants in Sanya. Diagnostic ratios of atmospheric PAHs further indicate that there was a wide mix of pollution sources in winter while fossil fuel combustion was the most dominant in summer. Positive Matrix Factorization (PMF) analysis with 18 PAHs in the winter samples found that motor vehicle emissions and biomass burning were the two main pollution sources, contributing 37.5% and 24.6% of the total quantified PAHs, respectively. - Highlights: • The first comprehensive study to investigate carbonaceous PM2.5 in Sanya, China • Higher carbonaceous levels in winter while more SOC formation in summer • Anthropogenic emission is the dominant sources of n-alkanes • Vehicle emission and biomass burning contributed ≥60% of the total PAHs in winter • The result supports better air quality in Sanya than most megacities in China

  1. Thermal characteristics and mass absorption efficiency of carbonaceous aerosol measured during a post-harvest burning period

    Science.gov (United States)

    Batmunkh, T.; Kim, Y. J.; Cayetano, M. G.; Lee, K.; Kim, K.; Park, K.

    2012-12-01

    In order to better understand the characteristics of carbonaceous aerosol time-resolved OC, EC, and BC were measured by a Sunset OC/EC analyzer and an Aethalometer, respectively, during a post-harvest burning period from November 22 to December 20, 2011 at a sub-urban site in Gwangju, Korea. OC and EC were analyzed by the thermal-optical transmittance (TOT) method with NIOSH temperature protocol. The spectral light absorption coefficient (babs) was determined based on the Aethalometer data. Overall average OC and EC concentrations were found to be 5.0±2.4 ugC/ m3 and 1.5±0.9 ugC/ m3, respectively for the sampling period. On average, babs at seven Aethalometer wavelengths was found to be 38.4±27.8 Mm-1, 24.3±17.8 Mm-1, 20.8±15.4 Mm-1, 17.9±13.3 Mm-1, 14.9±11.1 Mm-1, 9.9±7.4 Mm-1, and 8.8±6.6 Mm-1 at 370 nm, 470 nm, 520 nm, 590 nm, 660 nm, 880 nm, and 950 nm, respectively. Clear diurnal variations with morning (7:00 AM~9:00 AM) and evening (7:00 PM~11:00 PM) peaks were observed for OC, EC, and babs mostly due to local burning activities. Based on the 4-day back-trajectory analyses conducted using the HYSPLIT model. Event cases were classified into four categories, based on the 4-day air mass back trajectories, as Clean(C), Stagnant(ST), Continental(CC), and Local Burning(LB) events. In order to better investigate the characteristics of atmospheric carbonaceous aerosol, thermal evolution patterns of carbonaceous aerosol measured by the Sunset analyzer were characterized as OC1, OC2, and EC, which were detected in temperature steps of 600 C, 840 C in an non-oxidizing atmosphere, and 870 C in an oxidizing atmosphere, respectively. High ratio of OC2/OC1; 1.39~1.41 was observed in the evening 9:00~11:00 PM due to local burning event. Concentration of OC2 was higher up to 1.4 times than that of OC1 for the LB cases, showing that higher molecular weight fraction of organic aerosol was dominant for the time. As expected, higher correlation was found between EC and

  2. Chapter 3: Evaluating the impacts of carbonaceous aerosols on clouds and climate

    Energy Technology Data Exchange (ETDEWEB)

    Menon, Surabi; Del Genio, Anthony D.

    2007-09-03

    Any attempt to reconcile observed surface temperature changes within the last 150 years to changes simulated by climate models that include various atmospheric forcings is sensitive to the changes attributed to aerosols and aerosol-cloud-climate interactions, which are the main contributors that may well balance the positive forcings associated with greenhouse gases, absorbing aerosols, ozone related changes, etc. These aerosol effects on climate, from various modeling studies discussed in Menon (2004), range from +0.8 to -2.4 W m{sup -2}, with an implied value of -1.0 W m{sup -2} (range from -0.5 to -4.5 W m{sup -2}) for the aerosol indirect effects. Quantifying the contribution of aerosols and aerosol-cloud interactions remain complicated for several reasons some of which are related to aerosol distributions and some to the processes used to represent their effects on clouds. Aerosol effects on low lying marine stratocumulus clouds that cover much of the Earth's surface (about 70%) have been the focus of most of prior aerosol-cloud interaction effect simulations. Since cumulus clouds (shallow and deep convective) are short lived and cover about 15 to 20% of the Earth's surface, they are not usually considered as radiatively important. However, the large amount of latent heat released from convective towers, and corresponding changes in precipitation, especially in biomass regions due to convective heating effects (Graf et al. 2004), suggest that these cloud systems and aerosol effects on them, must be examined more closely. The radiative heating effects for mature deep convective systems can account for 10-30% of maximum latent heating effects and thus cannot be ignored (Jensen and Del Genio 2003). The first study that isolated the sensitivity of cumulus clouds to aerosols was from Nober et al. (2003) who found a reduction in precipitation in biomass burning regions and shifts in circulation patterns. Aerosol effects on convection have been included in

  3. Aerosol-generated mesoporous silicon oxycarbide particles

    International Nuclear Information System (INIS)

    Aerosol-generated mesoporous organosilica submicronic spheres have been converted into porous silicon oxycarbide (SiCO) glasses by pyrolysis at 1000 grad C in an inert atmosphere. Spherical mesoporous particles obtained from acidic solutions of 1,2-bis(triethoxysilyl) ethane and Pluronic F127 structuring agent were characterized by X-ray diffraction (XRD), transmission electron microscopy (TEM), N2 adsorption/desorption, and multi nuclear solid-state magic-angle spinning (MAS) NMR. These particles were then pyrolyzed at 1000 grad C and transformed into a SiCO phase as evidenced by 29Si MAS NMR, while TEM shows preserved mesoporosity, unfortunately difficult to access owing to the presence of an outer layer of dense silica. (authors)

  4. Ozone and secondary aerosol formation — Analysis of particle observations in the 2009 SHARP campaign

    Science.gov (United States)

    Cowin, J.; Yu, X.; Laulainen, N.; Iedema, M.; Lefer, B. L.; Anderson, D.; Pernia, D.; Flynn, J. H.

    2010-12-01

    Particulate matters (PM) play important roles in the formation and transformation of ozone. Although photooxidation of volatile organic compounds with respect to ozone formation in the gas phase is well understood, many unknowns still exist in heterogeneous mechanisms that process soot, secondary aerosols (both inorganic and organic), and key radical precursors such as formaldehyde and nitrous acid. Our main objective is to answer two key science questions: 1) will reduction of fine PM reduce ozone formation? 2) What sources of PM are most culpable? Are they from local chemistry or long-range transport? The field data collected in the 2009 Study of Houston Atmospheric Radical Precursors (SHARP) by our group at the Moody Tower consist of 1) real-time photolysis rates of ozone precursors, 2) particle size distributions, 3) organic carbon and elemental carbon, and 4) an archive of single particle samples taken with the Time Resolved Aerosol Collector (TRAC) sampler. The time resolution of the TRAC sampler is 30 minutes for routine measurements, and 15 minutes during some identified “events” (usually in the mid-afternoon) of high ozone and secondary organic or sulfate particle formation. The latter events last typically about an hour. Five ozone exceedance days occurred during the 6 weeks of deployment. Strong correlation between photochemical activities and organic carbon was observed. Initial data analysis indicates that secondary organic aerosol is a major component of the carbonaceous aerosols observed in Houston. Soot, secondary sulfate, seal salt, and mineral dust particles are determined from single particle analysis using scanning electron microscope and transmission electron microcopy coupled with energy dispersive X-ray spectroscopy. Compared with observations in 2000, the mass percentage of organics is higher (60 vs. 30%), and lower for sulfate (20% vs. 32%). On-going data analysis will focus on the composition, sources, and transformation of primary and

  5. Quantification of Optical and Physical Properties of Combustion-Generated Carbonaceous Aerosols (Analytical and Microscopic Techniques

    Science.gov (United States)

    Perera, Inoka Eranda; Litton, Charles D.

    2016-01-01

    A series of experiments were conducted to quantify and characterize the optical and physical properties of combustion-generated aerosols during both flaming and smoldering combustion of three materials common to underground mines—Pittsburgh Seam coal, Styrene Butadiene Rubber (a common mine conveyor belt material), and Douglas-fir wood—using a combination of analytical and gravimetric measurements. Laser photometers were utilized in the experiments for continuous measurement of aerosol mass concentrations and for comparison to measurements made using gravimetric filter samples. The aerosols of interest lie in the size range of tens to a few hundred nanometers, out of range of the standard photometer calibration. To correct for these uncertainties, the photometer mass concentrations were compared to gravimetric samples to determine if consistent correlations existed. The response of a calibrated and modified combination ionization/photoelectric smoke detector was also used. In addition, the responses of this sensor and a similar, prototype ionization/photoelectric sensor, along with discrete angular scattering, total scattering, and total extinction measurements, were used to define in real time the size, morphology, and radiative transfer properties of these differing aerosols that are generally in the form of fractal aggregates. SEM/TEM images were also obtained in order to compare qualitatively the real-time, continuous experimental measurements with the visual microscopic measurements. These data clearly show that significant differences exist between aerosols from flaming and from smoldering combustion and that these differences produce very different scattering and absorption signatures. The data also indicate that ionization/photoelectric sensors can be utilized to measure continuously and in real time aerosol properties over a broad spectrum of applications related to adverse environmental and health effects.

  6. Springtime carbon emission episodes at the Gosan background site revealed by total carbon, stable carbon isotopic composition, and thermal characteristics of carbonaceous particles

    Directory of Open Access Journals (Sweden)

    J. Jung

    2011-11-01

    Full Text Available In order to investigate the emission of carbonaceous aerosols at the Gosan background super-site (33.17° N, 126.10° E in East Asia, total suspended particles (TSP were collected during spring of 2007 and 2008 and analyzed for particulate organic carbon, elemental carbon, total carbon (TC, total nitrogen (TN, and stable carbon isotopic composition (δ13C of TC. The stable carbon isotopic composition of TC (δ13CTC was found to be lowest during pollen emission episodes (range: −26.2‰ to −23.5‰, avg. −25.2 ± 0.9‰, approaching those of the airborne pollen (−28.0‰ collected at the Gosan site. Based on a carbon isotope mass balance equation, we found that ~42% of TC in the TSP samples during the pollen episodes was attributed to airborne pollen from Japanese cedar trees planted around tangerine farms in Jeju Island. A negative correlation between the citric acid-carbon/TC ratios and δ13CTC was obtained during the pollen episodes. These results suggest that citric acid emitted from tangerine fruit may be adsorbed on the airborne pollen and then transported to the Gosan site. Thermal evolution patterns of organic carbon during the pollen episodes were characterized by high OC evolution in the OC2 temperature step (450 °C. Since thermal evolution patterns of organic aerosols are highly influenced by their molecular weight, they can be used as additional information on the formation of secondary organic aerosols and the effect of aging of organic aerosols during the long-range atmospheric transport and sources of organic aerosols.

  7. Characterization and sources of regional-scale transported carbonaceous and dust aerosols from different pathways in coastal and sandy land areas of China

    Science.gov (United States)

    Zhang, X. Y.; Wang, Y. Q.; Wang, D.; Gong, S. L.; Arimoto, R.; Mao, L. J.; Li, J.

    2005-08-01

    Concentrations of 12-hour averaged organic carbon (OC), elemental carbon (EC), and other trace elements were determined from bulk aerosol samples at a coastal city of Lian Yun Gang (LYG) in east China from June to December 2003 and a sandy land site of Tong Liao in northeast China from June to August 2003. Regional transports from four main source areas accounted for ˜35-49% of the Asian dust and 16-18% of the carbonaceous particles for both sites. The regional mean concentrations of various species, especially EC, were comparable to or lower than those in urban areas of inland China, Korea, and Japan but tended to be higher than those in Hong Kong or rural sites in east Asia. At LYG, OC showed a clear seasonal pattern with a peak loading in winter (24 μg m-3) and a low in summer (10 μg m-3). Seasonality of EC was more pronounced than that of OC with a difference of approximately threefold (3.8 to 11 μg m-3). Three types of air masses with high particulate loadings were found to be responsible for the peak EC and low OC/EC ratios in winter. Clean air masses with more than 50% secondary organic carbon contents were largely of marine origins. Elemental concentrations (Ca, Fe, K, Mn, and Ti) were mainly associated with Asian dust aerosols with a certain fraction of K from biomass burning in mainland China characterized with a ratio of 1.3 for OC/K.

  8. Contributions of vehicular carbonaceous aerosols to PM2.5 in a roadside environment in Hong Kong

    Science.gov (United States)

    Huang, X. H. H.; Bian, Q. J.; Louie, P. K. K.; Yu, J. Z.

    2014-09-01

    Hourly measurements of elemental carbon (EC) and organic carbon (OC) were made at Mong Kok, a roadside air quality monitoring station in Hong Kong, for a year, from May 2011 to April 2012. The monthly average EC concentrations were 3.8-4.9 μg C m-3, accounting for 9.2-17.7% of the PM2.5 mass (21.5-49.7 μg m-3). The EC concentrations showed little seasonal variation and peaked twice daily, coinciding with the traffic rush hours of a day. Strong correlations were found between EC and NOx concentrations, especially during the rush hours in the morning, confirming vehicular emissions as the dominant source of EC at this site. The analysis by means of the minimum OC / EC ratio approach to determine the OC / EC ratio representative of primary vehicular emissions yields a value of 0.5 for (OC / EC)vehicle. By applying the derived (OC / EC)vehicle ratio to the data set, the monthly average vehicle-related OC was estimated to account for 17-64% of the measured OC throughout the year. Vehicle-related OC was also estimated using receptor modeling of a combined data set of hourly NOx, OC, EC and volatile organic compounds characteristic of different types of vehicular emissions. The OCvehicle estimations by the two different approaches were in good agreement. When both EC and vehicle-derived organic matter (OM) (assuming an OM-to-OC ratio of 1.4) are considered, vehicular carbonaceous aerosols contributed ~ 7.3 μg m-3 to PM2.5, accounting for ~ 20% of PM2.5 mass (38.3 μg m-3) during winter, when Hong Kong received significant influence of air pollutants transported from outside, and ~ 30% of PM2.5 mass (28.2 μg m-3) during summertime, when local emission sources were dominant. A reduction of 3.8 μg m-3 in vehicular carbonaceous aerosols was estimated during 07:00-11:00 (i.e., rush hours on weekdays) on Sundays and public holidays. This could mainly be attributed to less on-road public transportation (e.g., diesel-powered buses) in comparison with non-holidays. These

  9. Enhanced UV Absorption in Carbonaceous Aerosols during MILAGRO and Identification of Potential Organic Contributors.

    Science.gov (United States)

    Mangu, A.; Kelley, K. L.; Marchany-Rivera, A.; Kilaparty, S.; Gunawan, G.; Gaffney, J. S.; Marley, N. A.

    2007-12-01

    Measurements of aerosol absorption were obtained as part of the MAX-Mex component of the MILAGRO field campaign at site T0 (Instituto Mexicano de Petroleo in Mexico City) during the month of March, 2006 by using a 7- channel aethalometer (Thermo-Anderson). These measurements, obtained at 370, 470, 520, 590, 660, 880, and 950 nm at a 5 minute time resolution, showed an enhanced absorption in the UV over that expected from carbon soot alone. Samples of fine atmospheric aerosols (less than 0.1micron) were also collected at site T0 and T1 (Universidad Technologica de Tecamac, State of Mexico) from 5 am to 5 pm (day) and from 5 pm to 5 am (night) during the month of March 2006. The samples were collected on quartz fiber filters with high volume impactor samplers. The samples have been characterized for total carbon content (stable isotope ratio mass spectroscopy) and natural radionuclide tracers (210Pb, 210Po, 210Bi, 7Be, 13C, 14C, 40K, 15N). Continuous absorption spectra of these aerosol samples have been obtained in the laboratory from 280 to 900nm with the use of an integrating sphere coupled to a UV-visible spectrometer (Beckman DU with a Labsphere accessory). The integrating sphere allows the detector to collect and spatially integrate the total radiant flux reflected from the sample and therefore allows for the measurement of absorption on highly reflective or diffusely scattering samples (1). The continuous spectra also show an enhanced UV absorption over that expected from carbon soot and the general profiles are quite similar to those observed for humic and fulvic acids found as colloidal materials in surface and groundwaters (2), indicating the presence of humic-like substances (HULIS) in the fine aerosols. The spectra also show evidence of narrow band absorbers below 400 nm typical of polycyclic aromatics (PAH) and nitrated aromatic compounds. Spectra were also obtained on NIST standard diesel soot (SRM 2975), NIST standard air particulate matter (SRM 8785

  10. Method of measuring aerosol particles using automated mobility-classified aerosol detector

    OpenAIRE

    Russell, Lynn M.; Flagan, Richard C.; Zhang, Shou-Hua

    1999-01-01

    An aerosol detection system for measuring particle number distribution with respect to particle dimension in an aerosol sample. The system includes an alternating dual-bag sampler, a radially classified differential mobility analyzer, and a condensation nucleus counter. Pressure variations in sampling are compensated by feedback control of volumetric flow rates.

  11. Elucidating determinants of aerosol composition through particle-type-based receptor modeling

    Directory of Open Access Journals (Sweden)

    M. L. McGuire

    2011-08-01

    Full Text Available An aerosol time-of-flight mass spectrometer (ATOFMS was deployed at a semi-rural site in southern Ontario to characterize the size and chemical composition of individual particles. Particle-type-based receptor modelling of these data was used to investigate the determinants of aerosol chemical composition in this region. Individual particles were classified into particle-types and positive matrix factorization (PMF was applied to their temporal trends to separate and cross-apportion particle-types to factors. The extent of chemical processing for each factor was assessed by evaluating the internal and external mixing state of the characteristic particle-types. The nine factors identified helped to elucidate the coupled interactions of these determinants. Nitrate-laden dust was found to be the dominant type of locally emitted particles measured by ATOFMS. Several factors associated with aerosol transported to the site from intermediate local-to-regional distances were identified: the Organic factor was associated with a combustion source to the north-west; the ECOC Day factor was characterized by nearby local-to-regional carbonaceous emissions transported from the south-west during the daytime; and the Fireworks factor consisted of pyrotechnic particles from the Detroit region following holiday fireworks displays. Regional aerosol from farther emissions sources was reflected through three factors: two Biomass Burning factors and a highly chemically processed Long Range Transport factor. The Biomass Burning factors were separated by PMF due to differences in chemical processing which were in part elucidated by the passage of two thunderstorm gust fronts with different air mass histories. The remaining two factors, ECOC Night and Nitrate Background, represented the night-time partitioning of nitrate to pre-existing particles of different origins. The distinct meteorological conditions observed during this month-long study in the summer of 2007

  12. Elucidating determinants of aerosol composition through particle-type-based receptor modeling

    Directory of Open Access Journals (Sweden)

    M. L. McGuire

    2011-03-01

    Full Text Available An aerosol time-of-flight mass spectrometer (ATOFMS was deployed at a semi-rural site in Southern Ontario to characterize the size and chemical composition of individual particles. Particle-type-based receptor modelling of these data was used to investigate the determinants of aerosol chemical composition in this region. Individual particles were classified into particle-types and positive matrix factorization (PMF was applied to their temporal trends to separate and cross-apportion particle-types to factors. The extent of chemical processing for each factor was assessed by evaluating the internal and external mixing state of the characteristic particle-types. The nine factors identified helped to elucidate the coupled interactions of these determinants. Nitrate-laden dust was found to be the dominant type of locally emitted particles measured by ATOFMS. Several factors associated with aerosol transported to the site from intermediate local-to-regional distances were identified: the Organic factor was associated with a combustion source to the north-west; the ECOC Day factor was characterized by nearby local-to-regional carbonaceous emissions transported from the south-west during the daytime; and the Fireworks factor consisted of pyrotechnic particles from the Detroit region following holiday fireworks displays. Regional aerosol from farther emissions sources were reflected through three factors: two biomass burning factors and a highly chemically processed long range transport factor. The biomass burning factors were separated by PMF due to differences in chemical processing which were caused in part by the passage of two thunderstorm gust fronts with different air mass histories. The remaining two factors, ECOC Night and Nitrate Background, represented the night-time partitioning of nitrate to pre-existing particles of different origins. The distinct meteorological conditions observed during this month-long study in the summer of 2007

  13. Emission factors for carbonaceous particles and polycyclic aromatic hydrocarbons from residential coal combustion in China.

    Science.gov (United States)

    Chen, Yingjun; Sheng, Guoying; Bi, Xinhui; Feng, Yanli; Mai, Bixian; Fu, Jiamo

    2005-03-15

    Emission factors of carbonaceous particles, including black carbon (BC) and organic carbon (OC), and polycyclic aromatic hydrocarbons (PAHs) were determined for five coals, which ranged in maturity from sub-bituminous to anthracite. They were burned in the form of honeycomb briquettes in a residential coalstove, one of the most common fuel/stove combinations in China. Smoke samples were taken through dilution sampling equipment, with a high volume sampler that could simultaneously collect emissions in both particulate and gaseous phases, and a cascade impactor that could segregate particles into six fractions. Particulate BC and OC were analyzed by a thermal-optical method, and PAHs in emissions of both phases were analyzed by GC-MS. Burning of bituminous coals produced the highest emission factors of particulate matter (12.91 g/kg), BC (0.28 g/kg), OC (7.82 g/kg), and 20 PAHs (210.6 mg/kg) on the basis of burned dry ash-free (daf) coal, while the anthracite honeycomb-briquette was the cleanest household coal fuel. The size-segregated results show that more than 94% of the particles were submicron, and calculated mass median aerodynamic diameters (MMAD) of all particles were under 0.3 microm. Based on the coal consumption in the residential sector of China, 290.24 Gg (gigagrams) of particulate matter, 5.36 Gg of BC, 170.33 Gg of OC, and 4.72 Gg of 20 PAHs mass were emitted annually from household honeycomb-briquette burning during 2000. Anthracite coal should be selected preferentially and more advanced burning conditions should be applied in domestic combustion, from the viewpoint of both climate change and adverse health effects. PMID:15819248

  14. Sources of carbonaceous aerosols over the United States and implications for natural visibility

    OpenAIRE

    Park, Rokjin J.; Jacob, Daniel James; Chin, Mian; Martin, Randall

    2003-01-01

    We use a global three-dimensional model (GEOS-CHEM) to better quantify the sources of elemental carbon (EC) and organic carbon (OC) aerosols in the United States through simulation of year-round observations for 1998 at a network of 45 sites (Interagency Monitoring of Protected Visual Environments (IMPROVE)). Simulation with our best a priori understanding of sources, including global satellite data to constrain fire emissions, captures most of the variance in the observations (R2 = 0.84 for ...

  15. Quantitative energy-dispersive electron probe X-ray microanalysis for single-particle analysis and its application for characterizing atmospheric aerosol particles

    Indian Academy of Sciences (India)

    Shila Maskey; Chul-Un Ro

    2011-02-01

    An energy-dispersive electron probe X-ray microanalysis (ED-EPMA) technique using an energy-dispersive X-ray detector with an ultra-thin window, designated as low-Z particle EPMA, has been developed. The low-Z particle EPMA allows the quantitative determination of concentrations of low-Z elements such as C, N and O, as well as higher-Z elements that can be analysed by conventional ED-EPMA. The quantitative determination of low-Z elements (using full Monte Carlo simulations, from the electron impact to the X-ray detection) in individual particles has improved the applicability of single-particle analysis, especially in atmospheric environmental aerosol research; many environmentally important atmospheric particles, e.g. sulphates, nitrates, ammonium and carbonaceous particles, contain low-Z elements. To demonstrate its practical applicability, the application of the low-Z particle EPMA for the characterization of Asian Dust, urban and subway aerosol particles is shown herein. In addition, it is demonstrated that the Monte Carlo calculation can also be applied in a quantitative single-particle analysis using transmission electron microscopy (TEM) coupled with energy-dispersive X-ray spectrometry (EDX), showing that the technique is useful and reliable for the characterization of submicron aerosol particles

  16. Determination of Aerosol Particle Diameter Using Cascade Impactor Procedure

    International Nuclear Information System (INIS)

    Determination of aerosol particle size distribution has been done using a low pressure Andersen's cascade impactor with 13 stages. The aerosol has been sampled with flow rate of aerosol sampling of 28.3 Ipm. Preliminary study result shows that aerosol in the simulation chamber was spread in monomodal distribution with Mass Median Aerodynamic Diameter of 4.9 μm. The aerosol measurement in Japan Power Demonstration Reactor has been spread in trimodal distribution with Activity Median Aerodynamic Diameter equal to 13.3 μm. The use of mylar as impaction plate instead of aluminum foil gives good result

  17. Carbonaceous aerosols recorded in a southeastern Tibetan glacier: analysis of temporal variations and model estimates of sources and radiative forcing

    Science.gov (United States)

    Wang, M.; Xu, B.; Cao, J.; Tie, X.; Wang, H.; Zhang, R.; Qian, Y.; Rasch, P. J.; Zhao, S.; Wu, G.; Zhao, H.; Joswiak, D. R.; Li, J.; Xie, Y.

    2015-02-01

    High temporal resolution measurements of black carbon (BC) and organic carbon (OC) covering the time period of 1956-2006 in an ice core over the southeastern Tibetan Plateau show a distinct seasonal dependence of BC and OC with higher respective concentrations but a lower OC / BC ratio in the non-monsoon season than during the summer monsoon. We use a global aerosol-climate model, in which BC emitted from different source regions can be explicitly tracked, to quantify BC source-receptor relationships between four Asian source regions and the southeastern Tibetan Plateau as a receptor. The model results show that South Asia has the largest contribution to the present-day (1996-2005) mean BC deposition at the ice-core drilling site during the non-monsoon season (October to May) (81%) and all year round (74%), followed by East Asia (14% to the non-monsoon mean and 21% to the annual mean). The ice-core record also indicates stable and relatively low BC and OC deposition fluxes from the late 1950s to 1980, followed by an overall increase to recent years. This trend is consistent with the BC and OC emission inventories and the fuel consumption of South Asia (as the primary contributor to annual mean BC deposition). Moreover, the increasing trend of the OC / BC ratio since the early 1990s indicates a growing contribution of coal combustion and/or biomass burning to the emissions. The estimated radiative forcing induced by BC and OC impurities in snow has increased since 1980, suggesting an increasing potential influence of carbonaceous aerosols on the Tibetan glacier melting and the availability of water resources in the surrounding regions. Our study indicates that more attention to OC is merited because of its non-negligible light absorption and the recent rapid increases evident in the ice-core record.

  18. Airborne measurements of carbonaceous aerosols in southern Africa during the dry, biomass burning season

    Energy Technology Data Exchange (ETDEWEB)

    Kirchstetter, Thomas W.; Novakov, T.; Hobbs, Peter V.; Magi, Brian

    2002-06-17

    Particulate matter collected aboard the University of Washington's Convair-580 research aircraft over southern Africa during the dry, biomass burning season was analyzed for total carbon, organic carbon, and black carbon contents using thermal and optical methods. Samples were collected in smoke plumes of burning savanna and in regional haze. A known artifact, produced by the adsorption of organic gases on the quartz filter substrates used to collect the particulate matter samples, comprised a significant portion of the total carbon collected. Consequently, conclusions derived from the data are greatly dependent on whether or not organic carbon concentrations are corrected for this artifact. For example, the estimated aerosol co-albedo (1 - single scattering albedo), which is a measure of aerosol absorption, of the biomass smoke samples is 60 percent larger using corrected organic carbon concentrations. Thus, the corrected data imply that the biomass smoke is 60 percent more absorbing than do the uncorrected data. The black carbon to (corrected) organic carbon mass ratio (BC/OC) of smoke plume samples (0.18/2610.06) is lower than that of samples collected in the regional haze (0.25/2610.08). The difference may be due to mixing of biomass smoke with background air characterized by a higher BC/OC ratio. A simple source apportionment indicates that biomass smoke contributes about three-quarters of the aerosol burden in the regional haze, while other sources (e.g., fossil fuel burning) contribute the remainder.

  19. Real time analysis of lead-containing atmospheric particles in Beijing during springtime by single particle aerosol mass spectrometry.

    Science.gov (United States)

    Ma, Li; Li, Mei; Huang, Zhengxu; Li, Lei; Gao, Wei; Nian, Huiqing; Zou, Lilin; Fu, Zhong; Gao, Jian; Chai, Fahe; Zhou, Zhen

    2016-07-01

    Using a single particle aerosol mass spectrometer (SPAMS), the chemical composition and size distributions of lead (Pb)-containing particles with diameter from 0.1 μm to 2.0 μm in Beijing were analyzed in the spring of 2011 during clear, hazy, and dusty days. Based on mass spectral features of particles, cluster analysis was applied to Pb-containing particles, and six major classes were acquired consisting of K-rich, carboneous, Fe-rich, dust, Pb-rich, and Cl-rich particles. Pb-containing particles accounted for 4.2-5.3%, 21.8-22.7%, and 3.2% of total particle number during clear, hazy and dusty days, respectively. K-rich particles are a major contribution to Pb-containing particles, varying from 30.8% to 82.1% of total number of Pb-containing particles, lowest during dusty days and highest during hazy days. The results reflect that the chemical composition and amount of Pb-containing particles has been affected by meteorological conditions as well as the emissions of natural and anthropogenic sources. K-rich particles and carbonaceous particles could be mainly assigned to the emissions of coal combustion. Other classes of Pb-containing particles may be associated with metallurgical processes, coal combustion, dust, and waste incineration etc. In addition, Pb-containing particles during dusty days were first time studied by SPAMS. This method could provide a powerful tool for monitoring and controlling of Pb pollution in real time. PMID:27085059

  20. Radiocarbon-based impact assessment of open biomass burning on regional carbonaceous aerosols in North China

    International Nuclear Information System (INIS)

    Samples of total suspended particulates (TSPs) and fine particulate matter (PM2.5) were collected from 29th May to 1st July, 2013 at a regional background site in Bohai Rim, North China. Mass concentrations of particulate matter and carbonaceous species showed a total of 50% and 97% of the measured TSP and PM2.5 levels exceeded the first grade national standard of China, respectively. Daily concentrations of organic carbon (OC) and elemental carbon (EC) were detected 7.3 and 2.5 μg m−3 in TSP and 5.2 and 2.0 μg m−3 in PM2.5, which accounted 5.8% and 2.0% of TSP while 5.6% and 2.2% for PM2.5, respectively. The concentrations of OC, EC, TSP and PM2.5 were observed higher in the day time than those in the night time. The observations were associated with the emission variations from anthropogenic activities. Two merged samples representing from south and north source areas were selected for radiocarbon analysis. The radiocarbon measurements showed 74% of water-insoluble OC (WINSOC) and 59% of EC in PM2.5 derived from biomass burning and biogenic sources when the air masses were from south region, and 63% and 48% for the air masses from north, respectively. Combined with backward trajectories and daily burned area, open burning of agricultural wastes was found to be predominating, which was confirmed by the potential source contribution function (PSCF). - Highlights: • PM2.5 and TSP samples collected at Yellow River Delta were analyzed for OC and EC. • OC, EC, TSP and PM2.5 concentrations were higher in daytime than in nighttime. • Radiocarbon (14C) tracer, backward trajectories, and fire counts were used for the analysis. • Agricultural waste open burning was a main contributor to summer PM2.5, OC and EC

  1. Spheroidal carbonaceous particles are a defining stratigraphic marker for the Anthropocene

    Science.gov (United States)

    Swindles, Graeme T.; Watson, Elizabeth; Turner, T. Edward; Galloway, Jennifer M.; Hadlari, Thomas; Wheeler, Jane; Bacon, Karen L.

    2015-05-01

    There has been recent debate over stratigraphic markers used to demarcate the Anthropocene from the Holocene Epoch. However, many of the proposed markers are found only in limited areas of the world or do not reflect human impacts on the environment. Here we show that spheroidal carbonaceous particles (SCPs), a distinct form of black carbon produced from burning fossil fuels in energy production and heavy industry, provide unambiguous stratigraphic markers of the human activities that have rapidly changed planet Earth over the last century. SCPs are found in terrestrial and marine sediments or ice cores in every continent, including remote areas such as the high Arctic and Antarctica. The rapid increase in SCPs mostly occurs in the mid-twentieth century and is contemporaneous with the ‘Great Acceleration’. It therefore reflects the intensification of fossil fuel usage and can be traced across the globe. We integrate global records of SCPs and propose that the global rapid increase in SCPs in sedimentary records can be used to inform a Global Standard Stratigraphic Age for the Anthropocene. A high-resolution SCP sequence from a lake or peatland may provide the much-needed ‘Golden Spike’ (Global Boundary Stratotype Section and Point).

  2. Use of stable carbon and nitrogen isotope ratios in size segregated aerosol particles for the O/I penetration evaluation

    Science.gov (United States)

    Garbaras, Andrius; Garbariene, Inga; Masalaite, Agne; Ceburnis, Darius; Krugly, Edvinas; Kvietkus, Kestutis; Remeikis, Vidmantas; Martuzevicius, Dainius

    2015-04-01

    Stable carbon and nitrogen isotope ratio are successfully used in the atmospheric aerosol particle source identification [1, 2], transformation, pollution [3] research. The main purpose of this study was to evaluate the penetration of atmospheric aerosol particles from outdoor to indoor using stable carbon and nitrogen isotope ratios. Six houses in Kaunas (Lithuania) were investigated during February and March 2013. Electrical low pressure impactor was used to measure in real time concentration and size distribution of outdoor aerosol particles. ELPI+ includes 15 channels covering the size range from 0.017 to 10.0 µm. The 25 mm diameter aluminium foils were used to collect aerosol particles. Gravimetric analysis of samples was made using microbalance. In parallel, indoor aerosol samples were collected with a micro-orifice uniform deposition impactor (MOUDI model 110), where the aerosol particles were separated with the nominal D50 cut-off sizes of 0.056, 0.1, 0.18,0.32,0.56, 1.0, 1.8, 3.2, 5.6, 10, 18 μm for impactor stages 1-11, respectively. The impactor was run at a flow rate of 30 L/min. Air quality meters were used to record meteorological conditions (temperature, relative humidity) during the investigated period. All aerosol samples were analyzed for total carbon (TC) and total nitrogen (TN) contents and their isotopic compositions using elemental analyzer (EA) connected to the stable isotope ratio mass spectrometer (IRMS). TC concentration in indoors ranged from 1.5 to 247.5 µg/m3. During the sampling period outdoors TN levels ranged from 0.1 to 10.9 µg/m3. The obtained outdoor δ13C(PM2.5) values varied from -24.21 to -26.3‰, while the δ15N values varied from 2.4 to 11.1 ‰ (average 7.2±2.5 ‰). Indoors carbonaceous aerosol particles were depleted in 13C compared to outdoors in all sampling sites. This depletion in δ13C varied from 0.1 to 3.2 ‰. We think that this depletion occurs due ongoing chemical reactions (oxidation) when aerosol

  3. An Unique On-line Method to Infer Black Carbonaceous contributions to Water-Insoluble Aerosol Compositions

    Science.gov (United States)

    Asa-Awuku, A. A.; Short, D.

    2013-12-01

    Particle number, size, and composition information is important for constraining aerosol effects on air quality, climate, and health. The composition of particles, especially from vehicular sources, may contain insoluble material that may modify particle nucleating properties. Changes in fuel properties are known to modify criteria pollutants and particulate matter mass, size, and number. In this work we summarize findings as they pertain to the water-soluble and insoluble composition of particles. In field measuremnts and controlled laboratory studies, a water-based condensation particle counter (CPC) and a butanol-based CPC measure particle number concentration. Both instruments were coupled with a Scanning Mobility Particle Sizer (SMPS) and particle number and size data were recorded. Real time particle insoluble mass fractions are estimated with the SMPS data sets; theoretical soluble fractions are calculated from ideal hygroscopicty single parameter values. This is the first time that this experimental method has been employed and used to infer online insoluble fractions. The results show that near-roadway emissions contain water insoluble and black carbon components. We will discuss the contributions of the organic component to the water-insoluble nature. Time permitting, the emissions of different ethanol and butanol gasoline blends are also explored for light-duty vehicles on a light-duty dynaometer chassis. Laboratory results indicate that soluble vehicular components are strongly correlated with vehicle driving conditions.

  4. Measurement of the electrostatic charge in airborne particles: II - particle charge distribution of different aerosols

    Directory of Open Access Journals (Sweden)

    M. V. Rodrigues

    2006-03-01

    Full Text Available This work gives sequence to the study on the measurement of the electrostatic charges in aerosols. The particle charge classifier developed for this purpose and presented in the previous paper (Marra and Coury, 2000 has been used here to measure the particle charge distribution of a number of different aerosols. The charges acquired by the particles were naturally derived from the aerosol generation procedure itself. Two types of aerosol generators were used: the vibrating orifice generator and turntable Venturi plate generator. In the vibrating orifice generator, mono-dispersed particles were generated by a solution of water/ethanol/methylene blue, while in the rotating plate generator, six different materials were utilized. The results showed no clear dependence between electric charge and particle diameter for the mono-dispersed aerosol. However, for the poly-dispersed aerosols, a linear dependence between particle size and charge could be noticed.

  5. Methods of analysis for complex organic aerosol mixtures from urban emission sources of particulate carbon

    International Nuclear Information System (INIS)

    Organic aerosols comprise approximately 30% by mass of the total fine particulate matter present in urban atmospheres. The chemical composition of such aerosols is complex and reflects input from multiple sources of primary emissions to the atmosphere, as well as from secondary production of carbonaceous aerosol species via photochemical reactions. To identify discrete sources of fine carbonaceous particles in urban atmospheres, analytical methods must reconcile both bulk chemical and molecular properties of the total carbonaceous aerosol fraction. This paper presents an overview of the analytical protocol developed and used in a study of the major sources of fine carbon particles emitted to an urban atmosphere. 23 refs., 1 fig., 2 tabs

  6. Sedimentary records of spheroidal carbonaceous particles from fossil-fuel combustion in western Lake Ontario

    Energy Technology Data Exchange (ETDEWEB)

    Lan, Y.L.; Breslin, V.T. [Syracuse University, Stony Brook, NY (USA). Marine Science Research Center

    1999-07-01

    Spheroidal carbonaceous particles (SCPs) were quantified in three sediment cores collected in the western basin of Lake Ontario to examine the impact of fossil-fuel combustion on sediment metal concentrations. SCP profiles were similar for the three cores showing the initiation of the SCP record deep in the core, followed by a rapid increase to a sub-surface maximum, and a subsequent decrease towards the sediment surface. Subsurface maximum SCP concentrations ranged from 1.97 to 5.61 x 10{sup 5} per gram dry matter/gDM. For Pb-210 dated cores, dates for the initiation of the SCP record (1850 {+-} 10 years), the initiation of the rapid rise in SCPs (1880 {+-} 13 years), and the SCP subsurface maximum (1961 {+-} 3 years) agree well. The rapid increase in sediment SCPs also agrees well with the US bituminous coal consumption during this same period (1880 to 1980). SCPs in surface sediments decreased between 55 to 83% from the subsurface maximum (1961 to 1996) in these cores while US coal usage continued to increase. SCP decreases were attributed to the increased use and efficiency of particle collection devices by utilities and industry. Lead, Cr, Cu, and Zn showed significant correlations with SCPs within each respective sediment core. Calculations show that although SCPs are not the major source of anthropogenic metals in Lake Ontario sediments, they may account for between 4 to 55% of the Zn, 1 to 12% of the Cu, 2 to 22% of the Pb and 1 to 18% of the Cr in these sediments.

  7. Radiocarbon-based impact assessment of open biomass burning on regional carbonaceous aerosols in North China

    Energy Technology Data Exchange (ETDEWEB)

    Zong, Zheng [Key Laboratory of Coastal Environmental Processes and Ecological Remediation, Yantai Institute of Coastal Zone Research, Chinese Academy of Sciences, Yantai 264003 (China); Graduate University of Chinese Academy of Sciences, Beijing 100039 (China); Chen, Yingjun, E-mail: yjchen@yic.ac.cn [Key Laboratory of Coastal Environmental Processes and Ecological Remediation, Yantai Institute of Coastal Zone Research, Chinese Academy of Sciences, Yantai 264003 (China); Tian, Chongguo, E-mail: cgtian@yic.ac.cn [Key Laboratory of Coastal Environmental Processes and Ecological Remediation, Yantai Institute of Coastal Zone Research, Chinese Academy of Sciences, Yantai 264003 (China); Fang, Yin [Key Laboratory of Coastal Environmental Processes and Ecological Remediation, Yantai Institute of Coastal Zone Research, Chinese Academy of Sciences, Yantai 264003 (China); Wang, Xiaoping [State Key Laboratory of Organic Geochemistry, Guangzhou Institute of Geochemistry, Chinese Academy of Sciences, Guangzhou 510640 (China); Graduate University of Chinese Academy of Sciences, Beijing 100039 (China); Huang, Guopei; Zhang, Fan [Key Laboratory of Coastal Environmental Processes and Ecological Remediation, Yantai Institute of Coastal Zone Research, Chinese Academy of Sciences, Yantai 264003 (China); Li, Jun; Zhang, Gan [State Key Laboratory of Organic Geochemistry, Guangzhou Institute of Geochemistry, Chinese Academy of Sciences, Guangzhou 510640 (China)

    2015-06-15

    Samples of total suspended particulates (TSPs) and fine particulate matter (PM{sub 2.5}) were collected from 29th May to 1st July, 2013 at a regional background site in Bohai Rim, North China. Mass concentrations of particulate matter and carbonaceous species showed a total of 50% and 97% of the measured TSP and PM{sub 2.5} levels exceeded the first grade national standard of China, respectively. Daily concentrations of organic carbon (OC) and elemental carbon (EC) were detected 7.3 and 2.5 μg m{sup −3} in TSP and 5.2 and 2.0 μg m{sup −3} in PM{sub 2.5}, which accounted 5.8% and 2.0% of TSP while 5.6% and 2.2% for PM{sub 2.5}, respectively. The concentrations of OC, EC, TSP and PM{sub 2.5} were observed higher in the day time than those in the night time. The observations were associated with the emission variations from anthropogenic activities. Two merged samples representing from south and north source areas were selected for radiocarbon analysis. The radiocarbon measurements showed 74% of water-insoluble OC (WINSOC) and 59% of EC in PM{sub 2.5} derived from biomass burning and biogenic sources when the air masses were from south region, and 63% and 48% for the air masses from north, respectively. Combined with backward trajectories and daily burned area, open burning of agricultural wastes was found to be predominating, which was confirmed by the potential source contribution function (PSCF). - Highlights: • PM{sub 2.5} and TSP samples collected at Yellow River Delta were analyzed for OC and EC. • OC, EC, TSP and PM{sub 2.5} concentrations were higher in daytime than in nighttime. • Radiocarbon ({sup 14}C) tracer, backward trajectories, and fire counts were used for the analysis. • Agricultural waste open burning was a main contributor to summer PM{sub 2.5}, OC and EC.

  8. Behaviour of Well Defined Aerosol Particles in a Test Chamber

    Czech Academy of Sciences Publication Activity Database

    Ondráček, Jakub; Brand, M.; Barták, M.; Ondráčková, Lucie; Smolík, Jiří

    -: -, 2009, T108A13. [European Aerosol Conference 2009. Karlsruhe (DE), 06.09.2009-11.09.2009] R&D Projects: GA ČR GA101/07/1361 Institutional research plan: CEZ:AV0Z40720504 Keywords : indoor aerosols * particle deposition * coagulation Subject RIV: CF - Physical ; Theoretical Chemistry

  9. The role of biomass burning in the budget and cycle of carbonaceous soot aerosols and their climate impact

    International Nuclear Information System (INIS)

    In this chapter, the authors estimate the climate impact from biomass burning due to both the direct radiative effects of smoke and the indirect effects on cloud albedo. They use the model of Walton et al. run in conjunction with the Lawrence Livermore National Laboratory version of the National Center for Atmospheric Research Community Climate Model 1 (NCAR CCM1). They describe the sources of aerosol particles from biomass burning as well as their soot content. After describing their model, they compare this latter quantity (or the predicted soot or black carbon concentration) to measured soot concentrations in the Southern Hemisphere. This provides a partial confirmation of their modeling procedures. Further confirmation of their predicted aerosol concentrations is also presented by comparing their predicted smoke optical depths with typical optical depths measured from satellites. Finally, the authors present the predicted change in outgoing solar radiation from biomass burning and summarize our estimate of the climate impact from biomass burning together with their conclusions

  10. Emission characteristics of carbonaceous particles from various residential coal-stoves in China.

    Science.gov (United States)

    Zhi, Guorui; Chen, Yingjun; Feng, Yanli; Xiong, Shengchun; Li, Jun; Zhang, Gan; Sheng, Guoying; Fu, Jiamo

    2008-05-01

    China is thought to be the most important contributor to the global burden of carbonaceous aerosols, and residential coal combustion is the greatest emission source of black carbon (BC). In the present study, two high-efficiency household coal-stoves are tested together with honeycomb-coal-briquettes and raw-coal-chunks of nine different coals. Coal-burning emissions are collected onto quartz fiber filters (QFFs) and analyzed by a thermal-optical transmittance (TOT) method. Emission factors (EFs) of particulate matter (PM), organic carbon (OC), and elemental carbon (EC) are systematically measured, and the average EFs are calculated by taking into account our previous data. For bituminous coal-briquette and -chunk, EFs of PM, OC, and EC are 7.33, 4.16, and 0.08 g/kg and 14.8, 5.93, and 3.81 g/kg, respectively; and for anthracite-briquette and -chunk, they are 1.21, 0.06, and 0.004 g/kg and 1.08, 0.10, and 0.007 g/kg, respectively. Annual estimates for PM, OC, and EC emissions in China are calculated for the years of 2000 and 2005 according to the EFs and coal consumptions, and the results are consistent with our previous estimates. Bituminous coal-chunk contributes 68% and 99% of the total OC and EC emissions from household coal burning, respectively. Additionally, a new model of Aethalometer (AE90) is introduced into the sampling system to monitor the real-time BC concentrations. On one hand, AE90 provides a set of EFs for optical BC in parallel to thermal-optical EC, and these two data are generally comparable, although BC/EC ratios vary in different coal/stove combinations. On the other hand, AE90 offers a chance to observe the variation of BC concentrations during whole burning cycles, which demonstrates that almost all BC emits into the flue during the initial period of 15 min after coal addition into household stoves. PMID:18522111

  11. Monodisperse Aerosol Particles in an Apartment

    Czech Academy of Sciences Publication Activity Database

    Ondráček, Jakub; Ondráčková, Lucie; Stavová, P.; Ždímal, Vladimír; Barták, M.; Smolík, Jiří

    Thessaloniki : Hellenic Association for Aerosol Research, 2008, T10A012P. [European Aerosol Conference 2008. Thessaloniki (GR), 24.08.2008-29.08.2008] R&D Projects: GA ČR GA101/07/1361 Institutional research plan: CEZ:AV0Z40720504 Keywords : indoor aerosols * dynamic characteristics * number size distribution Subject RIV: CF - Physical ; Theoretical Chemistry www.eac2008.org

  12. Numerical calculation of the optical properties for compound aerosol particles

    International Nuclear Information System (INIS)

    The atmosphere aerosol is an important part in earth and atmosphere system. The optical parameters are the important influence factors for evaluating atmospheric environment and studying the aerosol radiation climatic effect. They are also the key parameters for the research on the characteristics of laser propagation in atmosphere. According to the electrical structure of matter, the compound aerosol particles are dispersed into a series of dipoles, then by combining with discrete dipole approximation method and after obtaining the electric dipole moment of each dipole, the authors get the numerical results of the changes of extinction cross section, absorption cross section and asymmetry factor of spherical shape, ellipsoid shape and stratiform compound aerosol particles with wavelength, and made a comparative analysis of the optical parameter values for the ellipsoidal shape of single and composite components aerosol particles. The results show that all the incident wavelength, shape and component of aero- sol particles can affect the optical properties of aerosol particles. These can provides an efficiency approach and foundation for the research of the atmospheric optics, the aerosol climate radiative forcing effect, laser atmospheric transmission, etc. (authors)

  13. Basic phenomena utilised in aerosol particle measurement techniques; Hiukkasmittaustekniikoiden perusilmioet

    Energy Technology Data Exchange (ETDEWEB)

    Janka, K. [Dekati Oy, Tampere (Finland)

    2006-10-15

    The project deals with development of basic phenomena and mechanism utilised in aerosol particle measurement techniques. The areas under development are: particle-charging techniques, photoelectric charging, particle concentrating using virtual-impactor technique, and optical characterising techniques of particles. Results will be applied on detection techniques of bioaerosol attract, particle emission sensors for diesel exhaust gases, and widening the application areas of existing measurement techniques. (orig.)

  14. Gravitational agglomeration of post-HCDA LMFBR aerosols: nonspherical particles

    International Nuclear Information System (INIS)

    Aerosol behavior analysis computer programs have shown that temporal aerosol size distributions in nuclear reactor containments are sensitive to shape factors. This research investigates shape factors by a detailed theoretical analysis of hydrodynamic interactions between a nonspherical particle and a spherical particle undergoing gravitational collisions in an LMFBR environment. First, basic definitions and expressions for settling speeds and collisional efficiencies of nonspherical particles are developed. These are then related to corresponding quantities for spherical particles through shape factors. Using volume equivalent diameter as the defining length in the gravitational collision kernel, the aerodynamic shape factor, the density correction factor, and the gravitational collision shape factor, are introduced to describe the collision kernel for collisions between aerosol agglomerates. The Navier-Stokes equation in oblate spheroidal coordinates is solved to model a nonspherical particle and then the dynamic equations for two particle motions are developed. A computer program (NGCEFF) is constructed, and the dynamical equations are solved by Gear's method

  15. Development of aerosol transport and transformation models in PROFIT code. Coagulation of aerosol particles

    International Nuclear Information System (INIS)

    The problems of simulation of aerosol particles distribution in primary coolant circuit are discussed. The correlation dependences for collision centres and aerosol particles coagulation under the action of Brownian, turbulent, gradient and gravitational mechanisms with account of the accumulation effect are plotted. The dependences obtained take account of mutual influence of different coagulation mechanisms. The presented correlations for coagulation centre are implanted into PROFIT code

  16. Clustering of particles falling in a turbulent aerosol

    CERN Document Server

    Gustavsson, K; Mehlig, B

    2014-01-01

    Spatial clustering of identical particles falling through a turbulent aerosol enhances the collision rate between the falling particles, an important problem in aerosol science. We analyse this problem using perturbation theory in a dimensionless parameter, the so-called Kubo number. This allows us to derive an analytical theory quantifying the spatial clustering. We find that clustering of small particles in incompressible random velocity fields may be reduced or enhanced by the effect of gravity, depending on the Stokes number of the particles and the Froude number of the flow.

  17. Studies of aerosol particle formation from various sources using ion and electron beam analytical techniques.

    OpenAIRE

    Gharibi, Arash

    2006-01-01

    The thesis presents the results of studies of aerosol particle formation using ion and electron beam analytical techniques. The sources of aerosol particle formation studied are the following: 1. production of primary aerosol particles in the high Arctic region during summers 2. emission of ultrafine aerosol particles from wear on the road-tire interface 3. emission of aerosol particles from district heating units operating on three commonly-used biofuels. A source...

  18. Fossil and non-fossil source contributions to atmospheric carbonaceous aerosols during extreme spring grassland fires in Eastern Europe

    Science.gov (United States)

    Ulevicius, Vidmantas; Byčenkienė, Steigvilė; Bozzetti, Carlo; Vlachou, Athanasia; Plauškaitė, Kristina; Mordas, Genrik; Dudoitis, Vadimas; Abbaszade, Gülcin; Remeikis, Vidmantas; Garbaras, Andrius; Masalaite, Agne; Blees, Jan; Fröhlich, Roman; Dällenbach, Kaspar R.; Canonaco, Francesco; Slowik, Jay G.; Dommen, Josef; Zimmermann, Ralf; Schnelle-Kreis, Jürgen; Salazar, Gary A.; Agrios, Konstantinos; Szidat, Sönke; El Haddad, Imad; Prévôt, André S. H.

    2016-05-01

    In early spring the Baltic region is frequently affected by high-pollution events due to biomass burning in that area. Here we present a comprehensive study to investigate the impact of biomass/grass burning (BB) on the evolution and composition of aerosol in Preila, Lithuania, during springtime open fires. Non-refractory submicron particulate matter (NR-PM1) was measured by an Aerodyne aerosol chemical speciation monitor (ACSM) and a source apportionment with the multilinear engine (ME-2) running the positive matrix factorization (PMF) model was applied to the organic aerosol fraction to investigate the impact of biomass/grass burning. Satellite observations over regions of biomass burning activity supported the results and identification of air mass transport to the area of investigation. Sharp increases in biomass burning tracers, such as levoglucosan up to 683 ng m-3 and black carbon (BC) up to 17 µg m-3 were observed during this period. A further separation between fossil and non-fossil primary and secondary contributions was obtained by coupling ACSM PMF results and radiocarbon (14C) measurements of the elemental (EC) and organic (OC) carbon fractions. Non-fossil organic carbon (OCnf) was the dominant fraction of PM1, with the primary (POCnf) and secondary (SOCnf) fractions contributing 26-44 % and 13-23 % to the total carbon (TC), respectively. 5-8 % of the TC had a primary fossil origin (POCf), whereas the contribution of fossil secondary organic carbon (SOCf) was 4-13 %. Non-fossil EC (ECnf) and fossil EC (ECf) ranged from 13-24 and 7-13 %, respectively. Isotope ratios of stable carbon and nitrogen isotopes were used to distinguish aerosol particles associated with solid and liquid fossil fuel burning.

  19. Fossil and non-fossil source contributions to atmospheric carbonaceous aerosols during extreme spring grassland fires in Eastern Europe

    Directory of Open Access Journals (Sweden)

    V. Ulevicius

    2015-09-01

    Full Text Available In early spring the Baltic region is frequently affected by high pollution events due to biomass burning in that area. Here we present a comprehensive study to investigate the impact of biomass/grass burning (BB on the evolution and composition of aerosol in Preila, Lithuania, during springtime open fires. Non-refractory submicron particulate matter (NR-PM1 was measured by an Aerodyne aerosol chemical speciation monitor (ACSM and a source apportionment with the multilinear engine (ME-2 running the positive matrix factorization (PMF model was applied to the organic aerosol fraction to investigate the impact of biomass/grass burning. Satellite observations over regions of biomass burning activity supported the results and identification of air mass transport to the area of investigation. Sharp increases in biomass burning tracers, such as levoglucosan up to 683 ng m−3 and black carbon (BC up to 17 μg m−3 were observed during this period. A further separation between fossil and non-fossil primary and secondary contributions was obtained by coupling ACSM PMF results and radiocarbon (14C measurements of the elemental (EC and organic (OC carbon fractions. Non-fossil organic carbon (OCnf was the dominant fraction of PM1, with the primary (POCnf and secondary (SOCnf fractions contributing 26–44 % and 13–23 % to the TC, respectively. 5–8 % of the TC had a primary fossil origin (POCf, whereas the contribution of fossil secondary organic carbon (SOCf was 4–13 %. Non-fossil EC (ECnf and fossil EC (ECf ranged from 13–24 % and 7–12 %, respectively. Isotope ratio of stable carbon and nitrogen isotopes were used to distinguish aerosol particles associated with solid and liquid fossil fuel burning.

  20. 0D-modelling of carbonaceous aerosols; L'aerosol de combustion dans une region en grande mutation, l'Asie

    Energy Technology Data Exchange (ETDEWEB)

    Michel, Ch.

    2005-06-15

    One of the main uncertainties in the estimate of the climatic impact of aerosols is linked to our knowledge of gases and aerosols emissions. This is particularly crucial over Asia, where a strong regional fingerprint is observed, with different emission types, depending on the various vegetation and climate conditions (biomass burning emissions) and on the very fast changes of the population and industrialization (biofuel and fossil fuel emissions). The main goal of this work was first to derive a biomass burning inventory for gases and particles over Asia for the 2001 ACE-Asia (Aerosol Characterization Experiment) and TRACE-P (Transport and Chemical Evolution over the Pacific) campaigns (March to May 2001). I implemented a methodology that is the most adapted to my study, and based on the burnt area cartography (GBA-2000 project (Global Burnt Area 2000) [Tansey et al., 2005]). The results of this study, ABBI (Asian Biomass Burning Inventory) [Michel et al., 2005] have been compared with another biomass burning emission inventory (ACESS: ACE-Asia and TRACE-P Modelling and Emission Support System) [Streets et al., 2003], built from fire counts and not from burnt areas. This comparison shows the limits of the use of fire counts in the emission inventory maps and underlines the importance and the relevance of the method used in my study. A comparison with the year 2000 emission inventory, obtained with the same method, underlines the importance of the inter-annual variations. The ABBI inventory has been introduced in the Meso-NH-C mesoscale model combined with an aerosol module: ORISAM (ORganic and Inorganic Spectral Aerosol Module) Bessagnet, 2000]. I have focused in particular on the impact of the burnt vegetation emissions over the asian continent. Comparisons between simulated and ground and airborne measured data showed satisfactory results in some cases, but showed also some limits. Sensitivity tests have been carried out firstly to test the impact of fire

  1. Polarization resolved angular optical scattering of aerosol particles

    Science.gov (United States)

    Redding, B.; Pan, Y.; Wang, C.; Videen, G.; Cao, Hui

    2014-05-01

    Real-time detection and identification of bio-aerosol particles are crucial for the protection against chemical and biological agents. The strong elastic light scattering properties of airborne particles provides a natural means for rapid, non-invasive aerosol characterization. Recent theoretical predictions suggested that variations in the polarization dependent angular scattering cross section could provide an efficient means of classifying different airborne particles. In particular, the polarization dependent scattering cross section of aggregate particles is expected to depend on the shape of the primary particles. In order to experimentally validate this prediction, we built a high throughput, sampling system, capable of measuring the polarization resolved angular scattering cross section of individual aerosol particles flowing through an interrogating volume with a single shot of laser pulse. We calibrated the system by comparing the polarization dependent scattering cross section of individual polystyrene spheres with that predicted by Mie theory. We then used the system to study different particles types: Polystyrene aggregates composed 500 nm spheres and Bacillus subtilis (BG, Anthrax simulant) spores composed of elongated 500 nm × 1000 nm cylinder-line particles. We found that the polarization resolved scattering cross section depends on the shape of the constituent elements of the aggregates. This work indicates that the polarization resolved scattering cross section could be used for rapid discrimination between different bio-aerosol particles.

  2. Characteristics of aerosolized ice forming marine biogenic particles

    Science.gov (United States)

    Alpert, Peter A.

    Ice particles are ubiquitous in the atmosphere existing as the sole constituents of glaciated cirrus clouds or coexisting with supercooled liquid droplets in mixed-phase clouds. Aerosol particles serving as heterogeneous ice nuclei for ice crystal formation impact the global radiative balance by modification of cloud radiative properties, and thus climate. Atmospheric ice formation is not a well understood process and represents great uncertainty for climate prediction. The oceans which cover the majority of the earth's surface host nearly half the total global primary productivity and contribute to the greatest aerosol production by mass. However, the effect of biological activity on particle aerosolization, particle composition, and ice nucleation is not well established. This dissertation investigates the link between marine biological activity, aerosol particle production, physical/chemical particle characteristics, and ice nucleation under controlled laboratory conditions. Dry and humidified aerosol size distributions of particles from bursting bubbles generated by plunging water jets and aeration through frits in a seawater mesocosm containing bacteria and/or phytoplankton cultures, were measured as a function of biological activity. Total particle production significantly increases primarily due to enhanced aerosolization of particles ≤100 nm in diameter attributable to the presence and growth of phytoplankton. Furthermore, hygroscopicity measurements indicate primary organic material associated with the sea salt particles, providing additional evidence for the importance of marine biological activity for ocean derived aerosol composition. Ice nucleation experiments show that these organic rich particles nucleate ice efficiently in the immersion and deposition modes, which underscores their importance in mixed-phase and cirrus cloud formation processes. In separate ice nucleation experiments employing pure cultures of Thalassiosira pseudonana, Nannochloris

  3. Retrieval of particle size distribution from aerosol optical thickness using an improved particle swarm optimization algorithm

    Science.gov (United States)

    Mao, Jiandong; Li, Jinxuan

    2015-10-01

    Particle size distribution is essential for describing direct and indirect radiation of aerosols. Because the relationship between the aerosol size distribution and optical thickness (AOT) is an ill-posed Fredholm integral equation of the first type, the traditional techniques for determining such size distributions, such as the Phillips-Twomey regularization method, are often ambiguous. Here, we use an approach based on an improved particle swarm optimization algorithm (IPSO) to retrieve aerosol size distribution. Using AOT data measured by a CE318 sun photometer in Yinchuan, we compared the aerosol size distributions retrieved using a simple genetic algorithm, a basic particle swarm optimization algorithm and the IPSO. Aerosol size distributions for different weather conditions were analyzed, including sunny, dusty and hazy conditions. Our results show that the IPSO-based inversion method retrieved aerosol size distributions under all weather conditions, showing great potential for similar size distribution inversions.

  4. New apparatus of single particle trap system for aerosol visualization

    Science.gov (United States)

    Higashi, Hidenori; Fujioka, Tomomi; Endo, Tetsuo; Kitayama, Chiho; Seto, Takafumi; Otani, Yoshio

    2014-08-01

    Control of transport and deposition of charged aerosol particles is important in various manufacturing processes. Aerosol visualization is an effective method to directly observe light scattering signal from laser-irradiated single aerosol particle trapped in a visualization cell. New single particle trap system triggered by light scattering pulse signal was developed in this study. The performance of the device was evaluated experimentally. Experimental setup consisted of an aerosol generator, a differential mobility analyzer (DMA), an optical particle counter (OPC) and the single particle trap system. Polystylene latex standard (PSL) particles (0.5, 1.0 and 2.0 μm) were generated and classified according to the charge by the DMA. Singly charged 0.5 and 1.0 μm particles and doubly charged 2.0 μm particles were used as test particles. The single particle trap system was composed of a light scattering signal detector and a visualization cell. When the particle passed through the detector, trigger signal with a given delay time sent to the solenoid valves upstream and downstream of the visualization cell for trapping the particle in the visualization cell. The motion of particle in the visualization cell was monitored by CCD camera and the gravitational settling velocity and the electrostatic migration velocity were measured from the video image. The aerodynamic diameter obtained from the settling velocity was in good agreement with Stokes diameter calculated from the electrostatic migration velocity for individual particles. It was also found that the aerodynamic diameter obtained from the settling velocity was a one-to-one function of the scattered light intensity of individual particles. The applicability of this system will be discussed.

  5. Characteristics of carbonaceous aerosols in Emilia-Romagna (Northern Italy) based on two fall/winter field campaigns

    Science.gov (United States)

    Costa, V.; Bacco, D.; Castellazzi, S.; Ricciardelli, I.; Vecchietti, R.; Zigola, C.; Pietrogrande, M. C.

    2016-01-01

    The carbonaceous aerosol in Emilia-Romagna region (Northern Italy) was characterized in two fall/winter monitoring campaigns conducted through the years 2011-2012 and 2012-2013. Nearly 650 PM2.5 samples were collected at three monitoring stations describing urban background (main city Bologna, MS, Parma and Rimini) and one rural background site (San Pietro, SP). OC and EC values were measured by the thermal-optical transmittance method (TOT). Low flow-rate sampling strategy (24 m3 air volume per day) was used to reduce loading of light absorbing material on the filter surface in order to ensure the correct OC/EC discrimination. The TC values measured in winter 2011-2012 ranged from 9.8 μgC m- 3 at San Pietro to 12.0 μgC m- 3 at Parma, consisting of OC from 8.6 μgC m- 3 at SP to 9.9 μgC m- 3 at MS and EC from 1.3 μgC m- 3 at SP to 2.5 μgC m- 3 at Rimini. In winter 2012-2013, lower values were in general found with TC values ranging from 7.8 to 9.1 μgC m- 3 consisting of OC from 5.1 to 7.0 μgC m- 3 and EC from 1.5 to 2.2 μgC m- 3. Such differences can be likely explained by higher pollutant emissions related to domestic heating in colder fall/winter 2011/2012 (mean temperature ≈ 2 °C in comparison with ≈ 7 °C in winter 2012/2013). This hypothesis is supported by high levels of levoglucosan, as unambiguous tracer for biomass burning emission, and of polycyclic aromatic hydrocarbons related to combustion (levoglucosan ≃ 1000 ng m- 3 and burning PAHs ≃ 4 ng m- 3 at MS and SP sites).

  6. Characteristics and seasonal variation of Carbonaceous and Water soluble organic Components in the aerosols over East India

    Directory of Open Access Journals (Sweden)

    Basant Shubhankar

    2016-03-01

    Full Text Available The present investigation intends to measurement of PM2.5 and PM10 samples from agricultural (AG and an Adityapur industrial (AI site of East India to better characterize the carbonecous and water-soluble organic carbon (WSOC. The current study aimed (a to determine variation ratio of OC/PM, EC/PM, WSOC/EC, OC/EC in the study area (b assess and quantity the Correlation between OC and EC, WSOC and OC, WSOC and PM, WSOC and EC of AG and AI site (c Analyse the abundance pattern, at AG site indicating dominant contribution from biomass burning sources (wood-fuel and agriculture waste and in AI site sharp contrast influenced by emissions from coal-fired industries. The OC10/EC10, OC2.5/EC2.5, OC10/PM10, OC2.5/PM2.5, EC10/PM10,EC2.5/PM2.5 ratios at the AI and AG sampling sites varied from (min-max (average are 2.8 – 8.3 (4.9, 4.2 - 7.6 (5.5, 0.17 -0.19 (0.17, 0.14 - 0.20 (0.17, 0.03 - 0.06 (0.04, 0.02 - 0.04 (0.03 and 3.3 - 8.3 (4.9, 3.03 - 8.8 (3.9, 0.62 - 0.98 (0.78, 0.09 - 0.12 (0.09, 0.07 - 0.23 (0.17, 0.01 - 0.04 (0.02 respectively. Total carbon (TC was calculated as OC+EC. The comprehensive data set on EC, OC and WSOC/OC ratios from Eastern India is crucial to systematise the baseline data for future predictions of carbonaceous aerosol studies for atmospheric scattering and absorption of solar radiation on a regional scale.

  7. Major 20th century changes of carbonaceous aerosol components (EC, WinOC, DOC, HULIS, carboxylic acids, and cellulose) derived from Alpine ice cores

    Science.gov (United States)

    Legrand, M.; Preunkert, S.; Schock, M.; Cerqueira, M.; Kasper-Giebl, A.; Afonso, J.; Pio, C.; GelencséR, A.; Dombrowski-Etchevers, I.

    2007-12-01

    An extended array of carbonaceous species including elemental carbon (EC), water insoluble organic carbon (WinOC) as well as dissolved organic carbon (DOC), humic-like substances (HULIS), and single organic compounds like carboxylic acids, levoglucosan, and cellulose was investigated for the first time in Alpine snow deposits. These investigations were done on selected discrete ice cores sections extracted from Mount Rosa and Mount Blanc glaciers covering the 20th century and extending back to previous centuries. Here we focus on major changes in summer ice layers. Among carbonaceous components, EC reveals an outstanding increase with a sharp summer increase after World War II. This result is discussed against available past EC emission inventories in Europe which are thought to be mainly driven by emissions from road transport and residential sector. The long-term trend of organic carbon (OC) aerosol preserved in ice, WinOC as well as water soluble organic carbon (WSOC), was successfully reconstructed using the suitable array of organic compounds we investigated in this study. It is shown that the level of OC preserved in ice has increased by a factor of 2 after 1950 likely as a result of the enhancement of the oxidative capacity of the atmosphere over the last decades producing more secondary organic atmospheric aerosol from biogenic gaseous precursors.

  8. Nanostructured Aerosol Particles: Fabrication, Pulmonary Drug Delivery, and Controlled Release

    Directory of Open Access Journals (Sweden)

    Xingmao Jiang

    2011-01-01

    Full Text Available Pulmonary drug delivery is the preferred route of administration in the treatment of respiratory diseases and some nonrespiratory diseases. Recent research has focused on developing structurally stable high-dosage drug delivery systems without premature release. To maximize the deposition in the desired lung regions, several factors must be considered in the formulation. The special issue includes seven papers deal with aerosol-assisted fabrication of nanostructured particles, aerosol deposition, nanoparticles pulmonary exposure, and controlled release.

  9. Hygrosopicity measurements of aerosol particles in the San Joaquin Valley, CA, Baltimore, MD, and Golden, CO

    Science.gov (United States)

    Orozco, Daniel; Beyersdorf, A. J.; Ziemba, L. D.; Berkoff, T.; Zhang, Q.; Delgado, R.; Hennigan, C. J.; Thornhill, K. L.; Young, D. E.; Parworth, C.; Kim, H.; Hoff, R. M.

    2016-06-01

    Aerosol hygroscopicity was investigated using a novel dryer-humidifier system, coupled to a TSI-3563 nephelometer, to obtain the light scattering coefficient (σscat) as a function of relative humidity (RH) in hydration and dehydration modes. The measurements were performed in Porterville, CA (10 January to 6 February 2013), Baltimore, MD (3-30 July 2013), and Golden, CO (12 July to 10 August 2014). Observations in Porterville and Golden were part of the NASA-sponsored Deriving Information on Surface Conditions from Column and Vertically Resolved Observations Relevant to Air Quality project. The measured σscat under varying RH in the three sites was combined with ground aerosol extinction, PM2.5 mass concentrations, and particle composition measurements and compared with airborne observations performed during campaigns. The enhancement factor, f(RH), defined as the ratio of σscat(RH) at a certain RH divided by σscat at a dry value, was used to evaluate the aerosol hygroscopicity. Particles in Porterville showed low average f(RH = 80%) (1.42) which was attributed to the high carbonaceous loading in the region where residential biomass burning and traffic emissions contribute heavily to air pollution. In Baltimore, the high average f(RH = 80%) (2.06) was attributed to the large contribution of SO42- in the region. The lowest water uptake was observed in Golden, with an average f(RH = 80%) = 1.24 where organic carbon dominated the particle loading. Different empirical fits were evaluated using the f(RH) data. The widely used Kasten (gamma) model was found least satisfactory, as it overestimates f(RH) for RH fit with two power law curve fitting parameters c and k was found to replicate f(RH) accurately from the three sites. The relationship between the organic carbon mass and the species that are affected by RH and f(RH) was also studied and categorized.

  10. Study of the carbonaceous fraction of the atmospheric aerosol in Chamonix and St Jean de Maurienne: seasonal evolutions, source and chemical characteristics; Etude de la fraction carbonee de l'aerosol atmospherique a Chamonix et St Jean de Maurienne: evolutions saisonnieres, sources et caracteristiques chimiques

    Energy Technology Data Exchange (ETDEWEB)

    Aymoz, G.

    2005-03-15

    The atmospheric aerosols play an important role in the earth climatic system. They are also at the origin of air pollution problems in urban areas. However, their influence on the global climactic change, as well as their chemical properties in urban zone, is still very poorly known. One of the main reasons to that is the lack of information on one of the major components of aerosol, the carbonaceous matter. This work focuses on a better knowledge of this particulate carbonaceous matter. This study presents measurements of carbonaceous matter (OC and EC) in aerosol (PM10) performed within the framework of the program POVA, between February 2001 and June 2003 in Chamonix and St Jean de Maurienne (French Alps). This series represents one of the first of this type for basic sites of alpine valleys, characterized by emissions located in the bottom of the valleys and strong temperature inversions in winter, limiting the dispersion of pollutants. The POVA program, centred on the study of air pollution in these valleys, was proposed following the closing of the 'Tunnel du Mont Blanc', in 1999. One of the main objectives was to evaluate the sources of pollution by particles, in particular the share due to the international heavy duty traffic. We could establish that, on the two sites and while the international heavy duty traffic was not restored in the Chamonix Valley, this source represented approximately a third of the observed mass of particles, and was at the origin of a weaker fraction of the carbonaceous matter mass. The extremely primary character of the carbonaceous matter is a remarkable specificity of our sites. The source of carbonaceous matter represented by light vehicles emissions could not be studied. Then, it appears that combustion of biomass (probably from fireplaces) plays an important role, increased in the case of low temperatures, on the levels of pollution by particles. Lastly, the potential impact of the semi-volatile matter condensation

  11. Aerosol particle formation - meteorological and synoptic processes behind the event

    Energy Technology Data Exchange (ETDEWEB)

    Sogacheva, L.

    2008-07-01

    Aerosol particles in the atmosphere are known to significantly influence ecosystems, to change air quality and to exert negative health effects. Atmospheric aerosols influence climate through cooling of the atmosphere and the underlying surface by scattering of sunlight, through warming of the atmosphere by absorbing sun light and thermal radiation emitted by the Earth surface and through their acting as cloud condensation nuclei. Aerosols are emitted from both natural and anthropogenic sources. Depending on their size, they can be transported over significant distances, while undergoing considerable changes in their composition and physical properties. Their lifetime in the atmosphere varies from a few hours to a week. New particle formation is a result of gas-to-particle conversion. Once formed, atmospheric aerosol particles may grow due to condensation or coagulation, or be removed by deposition processes. In this thesis we describe analyses of air masses, meteorological parameters and synoptic situations to reveal conditions favourable for new particle formation in the atmosphere. We studied the concentration of ultrafine particles in different types of air masses, and the role of atmospheric fronts and cloudiness in the formation of atmospheric aerosol particles. The dominant role of Arctic and Polar air masses causing new particle formation was clearly observed at Hyytiaelae, Southern Finland, during all seasons, as well as at other measurement stations in Scandinavia. In all seasons and on multi-year average, Arctic and North Atlantic areas were the sources of nucleation mode particles. In contrast, concentrations of accumulation mode particles and condensation sink values in Hyytiaelae were highest in continental air masses, arriving at Hyytiaelae from Eastern Europe and Central Russia. The most favourable situation for new particle formation during all seasons was cold air advection after cold-front passages. Such a period could last a few days until the

  12. Calibration method for a photoacoustic system for real time source apportionment of light absorbing carbonaceous aerosol based on size distribution measurements

    Science.gov (United States)

    Utry, Noemi; Ajtai, Tibor; Pinter, Mate; Orvos, Peter I.; Szabo, Gabor; Bozoki, Zoltan

    2016-04-01

    In this study, we introduce a calibration method with which sources of light absorbing carbonaceous particulate matter (LAC) can be apportioned in real time based on multi wavelength optical absorption measurements with a photoacoustic system. The method is primary applicable in wintry urban conditions when LAC is dominated by traffic and biomass burning. The proposed method was successfully tested in a field campaign in the city center of Szeged, Hungary during winter time where the dominance of traffic and wood burning aerosol has been experimentally demonstrated earlier. With the help of the proposed calibration method a relationship between the measured Aerosol Angström Exponent (AAE) and the number size distribution can be deduced. Once the calibration curve is determined, the relative strength of the two pollution sources can be deduced in real time as long as the light absorbing fraction of PM is exclusively related to traffic and wood burning. This assumption is indirectly confirmed in the presented measurement campaign by the fact that the measured size distribution is composed of two unimodal size distributions identified to correspond to traffic and wood burning aerosols. The proposed method offers the possibility of replacing laborious chemical analysis with simple in-situ measurement of aerosol size distribution data.

  13. Synthesis of nanosized metal particles from an aerosol

    Directory of Open Access Journals (Sweden)

    Srećko R. Stopić

    2013-10-01

    Full Text Available The synthesis of metallic nanoparticles from the precursor solution of salts using the ultrasonic spray pyrolysis method was considered in this work. During the control of process parameters (surface tension and density, the concentration of solution, residence time of aerosol in the reactor, presence of additives, gas flow rate, decomposition temperature of aerosol, type of precursor and working atmosphere it is possible to guide the process in order to obtain powders with such a morphology which satisfies more complex requirements for the desired properties of advanced engineering materials.  Significant advance in the improvement of powder characteristics (lower particles sizes, better spheroidity, higher surface area was obtained by the application of the ultrasonic generator for the preparation of aerosols. Ultrasonic spray pyrolysis is performed by the action of a powerful source of ultrasound on the corresponding precursor solution forming the aerosol with a constant droplet size, which depends on the characteristics of liquid and the frequency of ultrasound. The produced aerosols were transported into the hot reactor, which enables the reaction to occur in a very small volume of a particle and formation of  nanosized powder. Spherical, nanosized particles of metals (Cu, Ag, Au, Co were produced with new and improved physical and chemical characteristics at the IME, RWTH Aachen University. The high costs associated with small quantities of produced nanosized particles represent a limitation of the USP-method. Therefore, scale up of the ultrasonic spray pyrolysis was performed as a final target in the synthesis of nanosized powder.

  14. Aerosol nucleation induced by a high energy particle beam

    DEFF Research Database (Denmark)

    Enghoff, Martin Andreas Bødker; Pedersen, Jens Olaf Pepke; Uggerhøj, Ulrik I.;

    2011-01-01

    We have studied sulfuric acid aerosol nucleation in an atmospheric pressure reaction chamber using a 580 MeV electron beam to ionize the volume of the reaction chamber. We find a clear contribution from ion-induced nucleation and consider this to be the first unambiguous observation of the ion-effect...... on aerosol nucleation using a particle beam under conditions that resemble the Earth's atmosphere. By comparison with ionization using a gamma source we further show that the nature of the ionizing particles is not important for the ion-induced component of the nucleation. This implies that...

  15. FTIR Analysis of Functional Groups in Aerosol Particles

    Science.gov (United States)

    Shokri, S. M.; McKenzie, G.; Dransfield, T. J.

    2012-12-01

    Secondary organic aerosols (SOA) are suspensions of particulate matter composed of compounds formed from chemical reactions of organic species in the atmosphere. Atmospheric particulate matter can have impacts on climate, the environment and human health. Standardized techniques to analyze the characteristics and composition of complex secondary organic aerosols are necessary to further investigate the formation of SOA and provide a better understanding of the reaction pathways of organic species in the atmosphere. While Aerosol Mass Spectrometry (AMS) can provide detailed information about the elemental composition of a sample, it reveals little about the chemical moieties which make up the particles. This work probes aerosol particles deposited on Teflon filters using FTIR, based on the protocols of Russell, et al. (Journal of Geophysical Research - Atmospheres, 114, 2009) and the spectral fitting algorithm of Takahama, et al (submitted, 2012). To validate the necessary calibration curves for the analysis of complex samples, primary aerosols of key compounds (e.g., citric acid, ammonium sulfate, sodium benzoate) were generated, and the accumulated masses of the aerosol samples were related to their IR absorption intensity. These validated calibration curves were then used to classify and quantify functional groups in SOA samples generated in chamber studies by MIT's Kroll group. The fitting algorithm currently quantifies the following functionalities: alcohols, alkanes, alkenes, amines, aromatics, carbonyls and carboxylic acids.

  16. Composition and formation of organic aerosol particles in the Amazon

    Science.gov (United States)

    Pöhlker, C.; Wiedemann, K.; Sinha, B.; Shiraiwa, M.; Gunthe, S. S.; Artaxo, P.; Gilles, M. K.; Kilcoyne, A. L. D.; Moffet, R. C.; Smith, M.; Weigand, M.; Martin, S. T.; Pöschl, U.; Andreae, M. O.

    2012-04-01

    We applied scanning transmission X-ray microscopy with near edge X-ray absorption fine structure (STXM-NEXAFS) analysis to investigate the morphology and chemical composition of aerosol samples from a pristine tropical environment, the Amazon Basin. The samples were collected in the Amazonian rainforest during the rainy season and can be regarded as a natural background aerosol. The samples were found to be dominated by secondary organic aerosol (SOA) particles in the fine and primary biological aerosol particles (PBAP) in the coarse mode. Lab-generated SOA-samples from isoprene and terpene oxidation as well as pure organic compounds from spray-drying of aqueous solution were measured as reference samples. The aim of this study was to investigate the microphysical and chemical properties of a tropical background aerosol in the submicron size range and its internal mixing state. The lab-generated SOA and pure organic compounds occurred as spherical and mostly homogenous droplet-like particles, whereas the Amazonian SOA particles comprised a mixture of homogeneous droplets and droplets having internal structures due to atmospheric aging. In spite of the similar morphological appearance, the Amazon samples showed considerable differences in elemental and functional group composition. According to their NEXAFS spectra, three chemically distinct types of organic material were found and could be assigned to the following three categories: (1) particles with a pronounced carboxylic acid (COOH) peak similar to those of laboratory-generated SOA particles from terpene oxidation; (2) particles with a strong hydroxy (COH) signal similar to pure carbohydrate particles; and (3) particles with spectra resembling a mixture of the first two classes. In addition to the dominant organic component, the NEXAFS spectra revealed clearly resolved potassium (K) signals for all analyzed particles. During the rainy season and in the absence of anthropogenic influence, active biota is

  17. Size distribution characteristics of carbonaceous aerosol in Xishuangbanna, southwest China: a sign for biomass burning in Asia.

    Science.gov (United States)

    Guo, Yuhong

    2016-03-01

    In 2012, size-segregated aerosol samples were collected in Xishuangbanna, a forest station in southwest China. The concentrations of organic and elemental carbon (OC and EC for short) were quantified with thermal/optical carbon analyzer in the filter samples. OC and EC exhibited similar seasonal patterns, with the highest concentrations in spring, possibly due to the influence of biomass burning in south and southeast Asia. The mass size distributions of OC and EC were bimodal in all the sampling seasons, each with a dominant peak in the fine mode of 0.4-0.7 μm and a coarse peak in the size range of 2.1-4.7 μm. In fine mode, OC and EC showed smaller geometric mean diameters (GMDs) during winter. OC and EC were prone to be more concentrated in fine particles in spring and winter than in summer and autumn. Furthermore, EC was more abundant in fine particles than OC. Good correlations (R (2) = 0.75-0.82) between OC and EC indicated that they had common dominant sources of combustion such as biomass burning and fossil fuel combustion emissions. The daily average OC/EC ratios ranged from 2.1 to 9.1, more elevated OC/EC ratios being found in the winter. PMID:26851952

  18. Selection of quasi-monodisperse super-micron aerosol particles

    Science.gov (United States)

    Rösch, Michael; Pfeifer, Sascha; Wiedensohler, Alfred; Stratmann, Frank

    2014-05-01

    Size-segregated quasi monodisperse particles are essential for e.g. fundamental research concerning cloud microphysical processes. Commonly a DMA (Differential Mobility Analyzer) is used to produce quasi-monodisperse submicron particles. Thereto first, polydisperse aerosol particles are bipolarly charged by a neutralizer, and then selected according to their electrical mobility with the DMA [Knutson et al. 1975]. Selecting a certain electrical mobility with a DMA results in a particle size distribution, which contains singly charged particles as well as undesired multiply charged larger particles. Often these larger particles need to either be removed from the generated aerosol or their signals have to be corrected for in the data inversion and interpretation process. This problem becomes even more serious when considering super-micron particles. Here we will present two different techniques for generating quasi-monodisperse super-micron aerosol particles with no or only an insignificant number of larger sized particles being present. First, we use a combination of a cyclone with adjustable aerodynamic cut-off diameter and our custom-built Maxi-DMA [Raddatz et al. 2013]. The cyclone removes particles larger than the desired ones prior to mobility selection with the DMA. This results in a reduction of the number of multiply charged particles of up to 99.8%. Second, we utilize a new combination of cyclone and PCVI (Pumped Counterflow Virtual Impactor), which is based on purely inertial separation and avoids particle charging. The PCVI instrument was previously described by Boulter et al. (2006) and Kulkarni et al. (2011). With our two setups we are able to produce quasi-monodisperse aerosol particles in the diameter range from 0.5 to 4.4 µm without a significant number of larger undesired particles being present. Acknowledgements: This work was done within the framework of the DFG funded Ice Nucleation research UnIT (INUIT, FOR 1525) under WE 4722/1-1. References

  19. Deposition of submicron aerosol particles in turbulent and transitional flow

    International Nuclear Information System (INIS)

    Brownian and turbulent diffusive deposition of submicron aerosol particles from pipe flow is studied experimentally and theoretically. A theoretical model for evaluating the turbulent diffusive deposition is presented in which a turbulent flow in a circular pipe is numerically calculated based on the k-ε turbulent flow model and deposition velocities are derived by solving the convection-diffusion equation. Deposition velocities of monodisperse aerosol particles, 0.01-0.04 μm in diameter, are obtained experimentally by measuring the decrease in the particle number concentration of an aerosol at two cross-sections of a circular test pipe through which the aerosol is flowing. The deposition velocities obtained when Re is larger than about 3,000 agree well with those predicted by the present analysis which are proportional to the 0.92nd power of Reynolds number and the 0.33rd power of Schmidt number. The particle deposition rates are measured when 1,000 approx-lt Re approx-lt 2,000 suggest a transitional state for particle deposition which cannot be explained by the present analysis nor by the laminar pipe flow deposition theory

  20. The characteristics and origins of carbonaceous aerosol at a rural site of PRD in summer of 2006

    Directory of Open Access Journals (Sweden)

    W. W. Hu

    2012-02-01

    Full Text Available Both organic carbon (OC and elemental carbon (EC were measured during PRIDE-PRD 2006 summer campaign by using a semi-continuous thermal-optical carbon analyzer at a rural site, Back Garden (BG, which is located 50 km to the northwest of Guangzhou City. Together with the online EC/OC analyzer, various kinds of instruments related to aerosol chemical properties were employed here, which provided a good opportunity to check data quality. The concentrations of OC correlated well with the mass of organic matter (OM and water soluble organic carbon (WSOC, implying the reliability of the data measured in this campaign. The average OC concentrations in fine particle for three typical periods during the campaign (local emission influence, typhoon and precipitation and normal days were 28.1 μgC m−3, 4.0 μgC m−3 and 5.7 μgC m−3, respectively; and EC were 11.6 μgC m−3, 1.8 μgC m−3, and 3.3 μgC m−3, respectively. The diurnal patterns of EC and OC during the campaign were higher at night and in early morning than daytime, which was probably caused by the primary emission and accumulation in the occurrence of low boundary layer. Compared with the constant diurnal enhancement ratios of EC, the enhancement ratio of OC (OC versus (CO-CObackground kept in a relative high level in the afternoon, with a similar diurnal profile to oxygenated organic aerosol (OOA, due to the strong photochemical formation of OC. Here, a modified EC tracer method was used to estimate the formation of secondary organic carbon (SOC. These results showed that the average SOC concentration (normal days at BG site was about 2.0 ± 2.3 μgC m−3, and the SOC fraction in OC could reach up to 80% with the average of 47%. The modified approach in this study proved to be effective and reliable for SOC estimation based on good correlations between estimated SOC versus OOA or WSOC, and

  1. Fossil vs. non-fossil sources of fine carbonaceous aerosols in four Chinese cities during the extreme winter haze episode of 2013

    Science.gov (United States)

    Zhang, Y.-L.; Huang, R.-J.; El Haddad, I.; Ho, K.-F.; Cao, J.-J.; Han, Y.; Zotter, P.; Bozzetti, C.; Daellenbach, K. R.; Canonaco, F.; Slowik, J. G.; Salazar, G.; Schwikowski, M.; Schnelle-Kreis, J.; Abbaszade, G.; Zimmermann, R.; Baltensperger, U.; Prévôt, A. S. H.; Szidat, S.

    2015-02-01

    During winter 2013, extremely high concentrations (i.e., 4-20 times higher than the World Health Organization guideline) of PM2.5 (particulate matter with an aerodynamic diameter China including Xi'an, Beijing, Shanghai and Guangzhou. Statistical analysis of a combined data set from elemental carbon (EC), organic carbon (OC), 14C and biomass-burning marker measurements using Latin hypercube sampling allowed a quantitative source apportionment of carbonaceous aerosols. Based on 14C measurements of EC fractions (six samples each city), we found that fossil emissions from coal combustion and vehicle exhaust dominated EC with a mean contribution of 75 ± 8% across all sites. The remaining 25 ± 8% was exclusively attributed to biomass combustion, consistent with the measurements of biomass-burning markers such as anhydrosugars (levoglucosan and mannosan) and water-soluble potassium (K+). With a combination of the levoglucosan-to-mannosan and levoglucosan-to-K+ ratios, the major source of biomass burning in winter in China is suggested to be combustion of crop residues. The contribution of fossil sources to OC was highest in Beijing (58 ± 5%) and decreased from Shanghai (49 ± 2%) to Xi'an (38 ± 3%) and Guangzhou (35 ± 7%). Generally, a larger fraction of fossil OC was from secondary origins than primary sources for all sites. Non-fossil sources accounted on average for 55 ± 10 and 48 ± 9% of OC and total carbon (TC), respectively, which suggests that non-fossil emissions were very important contributors of urban carbonaceous aerosols in China. The primary biomass-burning emissions accounted for 40 ± 8, 48 ± 18, 53 ± 4 and 65 ± 26% of non-fossil OC for Xi'an, Beijing, Shanghai and Guangzhou, respectively. Other non-fossil sources excluding primary biomass burning were mainly attributed to formation of secondary organic carbon (SOC) from non-fossil precursors such as biomass-burning emissions. For each site, we also compared samples from moderately to heavily

  2. Fossil vs. non-fossil sources of fine carbonaceous aerosols in four Chinese cities during the extreme winter haze episode in 2013

    Directory of Open Access Journals (Sweden)

    Y.-L. Zhang

    2014-10-01

    Full Text Available During winter 2013, extremely high concentrations (i.e. 4–20 times higher than the World Health Organization guideline of PM2.5 (particulate matter with an aerodynamic diameter 14C and biomass-burning marker measurements using Latin-hypercube sampling allowed a quantitative source apportionment of carbonaceous aerosols. We found that fossil emissions from coal combustion and vehicle exhaust dominated EC with a mean contribution of 75 ± 8% at all sites. The remaining 25 ± 8% was exclusively attributed to biomass combustion, consistent with the measurements of biomass-burning markers such as anhydrosugars (levoglucosan and mannosan and water-soluble potassium (K+. With a combination of the levoglucosan-to-mannosan and levoglucosan-to-K+ ratios, the major source of biomass burning in winter in China is suggested to be combustion of crop residues. The contribution of fossil sources to OC was highest in Beijing (58 ± 5% and decreased from Shanghai (49 ± 2% to Xian (38 ± 3% and Guangzhou (35 ± 7%. Generally, a larger fraction of fossil OC was rather from secondary origins than primary sources for all sites. Non-fossil sources accounted on average for 55 ± 10% and 48 ± 9% of OC and TC, respectively, which suggests that non-fossil emissions were very important contributors of urban carbonaceous aerosols in China. The primary biomass-burning emissions accounted for 40 ± 8%, 48 ± 18%, 53 ± 4% and 65 ± 26% of non-fossil OC for Xian, Beijing, Shanghai and Guangzhou, respectively. Other non-fossil sources excluding primary biomass-burning were mainly attributed to formation of secondary organic carbon (SOC from non-fossil precursors such as biomass-burning emissions. For each site, we also compared samples from moderately with heavily polluted days according to particulate matter mass. Despite a significant increase of absolute mass concentrations of primary emissions from both, fossil and non-fossil sources, during the heavily polluted events

  3. A 1 year record of carbonaceous aerosols from an urban site in the Indo-Gangetic Plain: Characterization, sources, and temporal variability

    Science.gov (United States)

    Ram, Kirpa; Sarin, M. M.; Tripathi, S. N.

    2010-12-01

    This study presents a comprehensive 1 year (January 2007-March 2008) data set on the chemical composition of ambient aerosols collected from an urban location (Kanpur) in the Indo-Gangetic Plain (IGP) and suggests that the varying strength of the regional emission sources, boundary layer dynamics, and formation of secondary aerosols all contribute significantly to the temporal variability in the mass concentrations of elemental carbon (EC), organic carbon (OC), and water-soluble OC (WSOC). On average, carbonaceous aerosols contribute nearly one third of the PM10 mass during winter, whereas their fractional mass is only ˜10% during summer. A three- to four-fold increase in the OC and K+ concentrations during winter and a significant linear relation between them suggest biomass burning (wood fuel and agricultural waste) emission as a dominant source. The relatively high OC/EC ratio (average: 7.4 ± 3.5 for n = 66) also supports that emissions from biomass burning are overwhelming for the particulate OC in the IGP. The WSOC/OC ratios vary from 0.21 to 0.70 over the annual seasonal cycle with relatively high ratios in the summer, suggesting the significance of secondary organic aerosols. The long-range transport of mineral aerosols from Iran, Afghanistan, and the Thar Desert (western India) is pronounced during summer months. The temporal variability in the concentrations of selected inorganic constituents and neutralization of acidic species (SO42- and NO3-) by NH4+ (dominant during winter) and Ca2+ (in summer) reflect conspicuous changes in the source strength of anthropogenic emissions.

  4. Modeling Dry Deposition of Aerosol Particles on Rough Surfaces

    Czech Academy of Sciences Publication Activity Database

    Hussein, T.; Smolík, Jiří; Kerminen, V.-M.; Kulmala, M.

    2012-01-01

    Roč. 46, č. 1 (2012), s. 44-59. ISSN 0278-6826 Institutional research plan: CEZ:AV0Z40720504 Keywords : aerosol particles * dry deposition * transport Subject RIV: CF - Physical ; Theoretical Chemistry Impact factor: 2.780, year: 2012

  5. Aerosol Particle Size Distributions at a Rural Coastal Site

    NARCIS (Netherlands)

    Leeuw, G. de; Vignati, E.

    1998-01-01

    Aerosol particle size distributions were measured on the Swedish island Ostergamsholm, about 3 km east of Gotland, from 26 April until 13 May, 1998. In this contribution preliminary results are presented of the dialysis of data collected at the south tip of the island at 10 m above sea level using a

  6. Mass Accomodation and Reactive uptake Coefficients for Nanoscale Aerosol Particles

    Czech Academy of Sciences Publication Activity Database

    Levdansky, V.V.; Smolík, Jiří; Ždímal, Vladimír; Moravec, Pavel

    - : -, 2013. ISBN N. [Research Workshop Nucleation Theory and Applications /17./. Dubna (RU), 01.04.2013-30.04.2013] R&D Projects: GA AV ČR IAA200760905 Institutional support: RVO:67985858 Keywords : aerosol particles * nanoscale * mass accommodation coefficient Subject RIV: CF - Physical ; Theoretical Chemistry

  7. Ice Nucleation Activity of Various Agricultural Soil Dust Aerosol Particles

    Science.gov (United States)

    Schiebel, Thea; Höhler, Kristina; Funk, Roger; Hill, Thomas C. J.; Levin, Ezra J. T.; Nadolny, Jens; Steinke, Isabelle; Suski, Kaitlyn J.; Ullrich, Romy; Wagner, Robert; Weber, Ines; DeMott, Paul J.; Möhler, Ottmar

    2016-04-01

    Recent investigations at the cloud simulation chamber AIDA (Aerosol Interactions and Dynamics in the Atmosphere) suggest that agricultural soil dust has an ice nucleation ability that is enhanced up to a factor of 10 compared to desert dust, especially at temperatures above -26 °C (Steinke et al., in preparation for submission). This enhancement might be caused by the contribution of very ice-active biological particles. In addition, soil dust aerosol particles often contain a considerably higher amount of organic matter compared to desert dust particles. To test agricultural soil dust as a source of ice nucleating particles, especially for ice formation in warm clouds, we conducted a series of laboratory measurements with different soil dust samples to extend the existing AIDA dataset. The AIDA has a volume of 84 m3 and operates under atmospherically relevant conditions over wide ranges of temperature, pressure and humidity. By controlled adiabatic expansions, the ascent of an air parcel in the troposphere can be simulated. As a supplement to the AIDA facility, we use the INKA (Ice Nucleation Instrument of the KArlsruhe Institute of Technology) continuous flow diffusion chamber based on the design by Rogers (1988) to expose the sampled aerosol particles to a continuously increasing saturation ratio by keeping the aerosol temperature constant. For our experiments, soil dust was dry dispersed into the AIDA vessel. First, fast saturation ratio scans at different temperatures were performed with INKA, sampling soil dust aerosol particles directly from the AIDA vessel. Then, we conducted the AIDA expansion experiment starting at a preset temperature. The combination of these two different methods provides a robust data set on the temperature-dependent ice activity of various agriculture soil dust aerosol particles with a special focus on relatively high temperatures. In addition, to extend the data set, we investigated the role of biological and organic matter in more

  8. Atmospheric aerosol particle analysis at the Debrecen Nuclear Microprobe

    International Nuclear Information System (INIS)

    Complete text of publication follows. Characterisation of atmospheric aerosol is in the focus of several national and international research programs due to their health impact and effects on the radiative balance of Earth. Bulk elemental analytical techniques, like macro-PIXE, are extensively used for analysing atmospheric aerosol. However more detailed and reliable data can be obtained if individual aerosol particles are analysed. Nuclear microscopy is a powerful tool which enables the quantitative determination of trace element distribution in complex samples with a sensitivity of μg/g on micrometer scale. In the frame of an OTKA and a Coordinated Research Project of the IAEA, an experimental setup based on the simultaneous use of different ion beam analytical techniques was developed at the Debrecen scanning nuclear microprobe facility, which enables the total quantitative analysis of microparticles. This measurement, data collection and evaluation setup was already applied successfully in various studies: (1) ion beam microanalysis of desert dust particles originating from Saharan dust intrusions, (2) characterization of urban aerosol sources by single particle analysis, (3) characterization of indoor aerosols. As an example, nuclear microprobe study of indoor aerosol particles containing toxic metals is presented. Aerosol samples were collected in the IBA Lab of ATOMKI in the frame of a laboratory practice for undergraduate students. At the same time mechanical repair work was carried out on the heating system in the corridor outside the Laboratory. In order to demonstrate the monitoring of air pollution for the students, aerosol samples were collected with a 2-stage filter unit on Nuclepore polycarbonate filters. The samples were analysed by bulk-PIXE. Concentration of Zn, Cd and Pb were found to be exceeding the national air quality limit. Therefore single particle analysis was carried out on the coarse mode samples to find out the origin of the toxic

  9. Chemical Composition of Organic Aerosol Particles over the Remote Ocean

    Science.gov (United States)

    Russell, L. M.; Frossard, A. A.; Keene, W. C.; Kieber, D. J.; Quinn, P.; Bates, T. S.

    2012-12-01

    Marine aerosol particles play an important role in Earth's radiative balance, yet the composition of the organic fraction of these important particles remains largely unconstrained. The composition of marine aerosol particles was measured in remote marine regions on board the R/V Atlantis during the CalNex 2010 campaign in May and June 2010, on board the R/V Point Sur during the E-PEACE campaign in July 2011, and on board the R/V Ronald Brown during the WACS campaign in August 2012. To understand the factors that control this composition, we compared the organic components of these particles to models of primary marine aerosol - i.e. those generated from bubbled and atomized seawater. The organic chemical composition was characterized by Fourier Transform Infrared (FTIR) spectroscopy to determine the functional group composition and high resolution time of flight aerosol mass spectrometer (HR-ToF-AMS) to identify characteristic mass fragments. Cluster analysis of FTIR organic spectra was used to identify different spectral signatures associated with location, seawater composition, and ambient conditions. Typical submicron organic mass (OM) concentrations were less than 0.80 μg m-3. The overall organic compositions of marine aerosol particles and generated seawater models were similar, with large fractions of organic hydroxyl functional groups in each. One cluster of FTIR spectra from the eastern Pacific showed the highest fraction of hydroxyl functional groups (77%) occurred during periods of high chlorophyll concentrations and high wind speeds (more than 10 m s-1). Detailed spectral comparisons revealed unique minor features that may be driven both by meteorology and regional differences in seawater composition for these and past studies.

  10. Dispersion of aerosol particles in the atmosphere: Fukushima

    Science.gov (United States)

    Haszpra, Tímea; Lagzi, István; Tél, Tamás

    2013-04-01

    Investigation of dispersion and deposition of aerosol particles in the atmosphere is an essential issue, because they have an effect on the biosphere and atmosphere. Moreover, aerosol particles have different transport properties and chemical and physical transformations in the atmosphere compared to gas phase air pollutants. The motion of a particle is described by a set of ordinary differential equations. The large-scale dynamics in the horizontal direction can be described by the equations of passive scalar advection, but in the vertical direction a well-defined terminal velocity should be taken into account as a term added to the vertical wind component. In the planetary boundary layer turbulent diffusion has an important role in the particle dispersion, which is taken into account by adding stochastic terms to the deterministic equations above. Wet deposition is also an essential process in the lower levels of the atmosphere, however, its precise parameterization is a challenge. For the simulations the wind field and other necessary data were taken from the ECMWF ERA-Interim database. In the case of the Fukushima Daiichi nuclear disaster (March-April 2011) radioactive aerosol particles were also released in the planetary boundary layer. Simulations (included the continuous and varying emission from the nuclear power plant) will be presented for the period of 14-23 March. Results show that wet deposition also has to be taken into consideration in the lower levels of the atmosphere. Furthermore, dynamical system characteristics are evaluated for the aerosol particle dynamics. The escape rate of particles was estimated both with and without turbulent diffusion, and in both cases when there was no wet deposition and also when wet deposition was taken into consideration.

  11. Visualizing aerosol-particle injection for diffractive-imaging experiments

    CERN Document Server

    Awel, Salah; Eckerskorn, Niko; Wiedorn, Max; Horke, Daniel A; Rode, Andrei V; Küpper, Jochen; Chapman, Henry N

    2015-01-01

    Delivering sub-micrometer particles to an intense x-ray focus is a crucial aspect of single-particle diffractive-imaging experiments at x-ray free-electron lasers. Enabling direct visualization of sub-micrometer aerosol particle streams without interfering with the operation of the particle injector can greatly improve the overall efficiency of single-particle imaging experiments by reducing the amount of time and sample consumed during measurements. We have developed in-situ non-destructive imaging diagnostics to aid real-time particle injector optimization and x-ray/particle-beam alignment, based on laser illumination schemes and fast imaging detectors. Our diagnostics are constructed to provide a non-invasive rapid feedback on injector performance during measurements, and have been demonstrated during diffraction measurements at the FLASH free-electron laser.

  12. A one-year record of carbonaceous components and major ions in aerosols from an urban kerbside location in Oporto, Portugal.

    Science.gov (United States)

    Custódio, Danilo; Cerqueira, Mário; Alves, Célia; Nunes, Teresa; Pio, Casimiro; Esteves, Valdemar; Frosini, Daniele; Lucarelli, Franco; Querol, Xavier

    2016-08-15

    PM2.5 aerosol samples were collected from January 2013 to January 2014 on the kerbside of a major arterial route in the city of Oporto, Portugal, and later analyzed for carbonaceous fractions and water soluble ions. The average concentrations of organic carbon (OC), elemental carbon (EC) and water soluble organic carbon (WSOC) in the aerosol were 6.2μg/m(3), 5.0μg/m(3) and 3.8μg/m(3), respectively, and fit within the range of values that have been observed close to major roads in Europe, Asia and North America. On average, carbonaceous matter accounted for 56% of the gravimetrically measured PM2.5 mass. The three carbon fractions exhibited a similar seasonal variation, with high concentrations in late autumn and in winter, and low concentrations in spring. SO4(2-) was the dominant water soluble ion, followed by NO3(-), NH4(+), Cl(-), Na(+), K(+), oxalate, Ca(2+), Mg(2+), formate, methanesulfonate and acetate. Some of these ions exhibited a clear seasonal trend during the study period. The average OC/EC ratio for the entire set of samples was 1.28±0.61, which was consistent with a significant influence of vehicle exhaust emissions on aerosol composition. On the other hand, the average WSOC/OC ratio was 0.67±0.23, reflecting the influence of other emitting sources. WSOC was highly correlated with nssK(+), a tracer of biomass combustion, and was not correlated with nssSO4(2-), a species associated with secondary processes, suggesting that the main source of WSOC was biomass burning. Most of the SO4(2-) was anthropogenic in origin and was closely associated with NH4(+), pointing to the formation of secondary aerosols. Na(+), Cl(-) and methanesulfonate were clearly associated with marine sources while NO3(-) was related with combustion of both fossil and non-fossil fuels. Mixed sources explained the occurrence of the other water soluble ions. PMID:27110993

  13. Surface Chemistry at Size-Selected Nano-Aerosol Particles

    Science.gov (United States)

    Roberts, Jeffrey

    2005-03-01

    A method has been developed to conduct surface chemistry and extract surface kinetic rates from size-selected aerosol nanoparticles. The measurements encompass broad ranges of particle size, phase, and composition. Results will be presented on the uptake of water by aerosolized soot nanoparticles of radius between 10 and 40 nm. Water uptake was monitored by tandem differential mobility analysis (T-DMA), which is capable of measuring changes in particle diameter as little as 0.2 nm. Soot particles were produced in an ethene diffusion flame and extracted into an atmospheric pressure aerosol flow tube reactor. The particles were subjected to various thermal and oxidative treatments, and the effects of these treatments on the ability of soot to adsorb monolayer quantities of water was determined. The results are important because soot nucleates atmospheric cloud particles. More generally, the results represent one of the first kinetic and mechanistic studies of gas-phase nanoparticle reactivity. Co-author: Henry Ajo, University of Minnesota

  14. Endotoxin in Size-Separated Metal Working Fluid Aerosol Particles.

    Science.gov (United States)

    Dahlman-Höglund, Anna; Lindgren, Åsa; Mattsby-Baltzer, Inger

    2016-08-01

    Patients with airway symptoms working in metal working industries are increasing, despite efforts to improve the environmental air surrounding the machines. Our aim was to analyse the amount of endotoxin in size-separated airborne particles of metal working fluid (MWF) aerosol, by using the personal sampler Sioutas cascade impactor, to compare filter types, and to compare the concentration of airborne endotoxin to that of the corresponding MWFs. In a pilot field study, aerosols were collected in two separate machine halls on totally 10 occasions, using glass fibre and polytetrafluoroethylene (PTFE) filters in parallel at each station. Airborne endotoxin was distributed over all size fractions. While a major part was found in the largest size fraction (72%, 2.5-10 µm), up to 8% of the airborne endotoxin was detected in the smallest size fraction (efficiency of the filter types, a significantly higher median endotoxin level was found with glass fibres filters collecting the largest particle-size fraction (1.2-fold) and with PTFE filters collecting the smallest ones (5-fold). The levels of endotoxin in the size-separated airborne particle fractions correlated to those of the MWFs supporting the aerosol-generating machines. Our study indicates that a significant part of inhalable aerosols of MWFs consists of endotoxin-containing particles below the size of intact bacteria, and thus small enough to readily reach the deepest part of the lung. Combined with other chemical irritants of the MWF, exposure to MWF aerosols containing endotoxin pose a risk to respiratory health problems. PMID:27268595

  15. The generation of particles with a vibrating reed aerosol generator

    International Nuclear Information System (INIS)

    The adhesion of contaminant particles to surfaces is a major problem in many industries. The strength of adhesion is dependent on the physical and chemical properties of the individual particles and those of the surface. The purpose of this project is to develop a sampling protocol to reproducibly remove particles from a surface thereby qualitatively measuring the adhesion strength. The suspended particles are subsequently collected and characterized by electron microscopy. The measurement of adhesion strength and subsequent characterization will enhance our understanding of adhesion of particles to surfaces. The approach towards development of a sampling protocol is to direct a stream of clean gas of known velocity on to a surface at varying angles, where particles have been previously deposited. The initial task is the development of a generator of monodisperse particles of known composition that can be deposited on a well defined surface. The authors have begun construction of a vibrating reed aerosol generator. The generator is based on the principal that a thin wire sweeps through a solution reservoir detaching droplets which on evaporation produce a stream of dry, solid particles of uniform size. The operational parameters of this aerosol generating system have been explored

  16. Chemical evolution of multicomponent aerosol particles during evaporation

    Science.gov (United States)

    Zardini, Alessandro; Riipinen, Ilona; Pagels, Joakim; Eriksson, Axel; Worsnop, Douglas; Switieckli, Erik; Kulmala, Markku; Bilde, Merete

    2010-05-01

    Atmospheric aerosol particles have an important but not well quantified effect on climate and human health. Despite the efforts made in the last decades, the formation and evolution of aerosol particles in the atmosphere is still not fully understood. The uncertainty is partly due to the complex chemical composition of the particles which comprise inorganic and organic compounds. Many organics (like dicarboxylic acids) can be present both in the gas and in the condensed phase due to their low vapor pressure. Clearly, an understanding of this partition is crucial to address any other issue in atmospheric physics and chemistry. Moreover, many organics are water soluble, and their influence on the properties of aqueous solution droplets is still poorly characterized. The solid and sub-cooled liquid state vapor pressures of some organic compounds have been previously determined by measuring the evaporation rate of single-compound crystals [1-3] or binary aqueous droplets [4-6]. In this work, we deploy the HTDMA technique (Hygroscopicity Tandem Differential Mobility Analyzer) coupled with a 3.5m laminar flow-tube and an Aerosol Mass Spectrometer (AMS) for determining the chemical evolution during evaporation of ternary droplets made of one dicarboxylic acid (succinic acid, commonly found in atmospheric samples) and one inorganic compound (sodium chloride or ammonium sulfate) in different mixing ratios, in equilibrium with water vapor at a fixed relative humidity. In addition, we investigate the evaporation of multicomponent droplets and crystals made of three organic species (dicarboxylic acids and sugars), of which one or two are semi-volatile. 1. Bilde M. and Pandis, S.N.: Evaporation Rates and Vapor Pressures of Individual Aerosol Species Formed in the Atmospheric Oxidation of alpha- and beta-Pinene. Environmental Science and Technology, 35, 2001. 2. Bilde M., et al.: Even-Odd Alternation of Evaporation Rates and Vapor Pressures of C3-C9 Dicarboxylic Acid Aerosols

  17. Two-photon excited fluorescence from biological aerosol particles

    International Nuclear Information System (INIS)

    We used a 40 MHz mode-locked 524 nm laser source to evaluate the utility of sub-picosecond excitation of fluorescence from 2-photon absorption in biological aerosols. Individual particles of biological composition, as well as other calibration particles, suspended in an inlet air flow were illuminated and measured as they passed through an optical chamber. To our knowledge, this was the first demonstration of 2-photon excited fluorescence from micron-sized particles composed of micro-organisms. We also observed a high fluorescence signal at visible wavelengths, which was not present with single-photon excitation.

  18. Aerosol nucleation induced by a high energy particle beam

    DEFF Research Database (Denmark)

    Enghoff, Martin Andreas Bødker; Pedersen, Jens Olaf Pepke; Uggerhøj, Ulrik I.;

    The effect of ions in aerosol nucleation is a subject where much remains to be discovered. That ions can enhance nucleation has been shown by theory, observations, and experiments. However, the exact mechanism still remains to be determined. One question is if the nature of the ionization affects...... the nucleation. This is an essential question since many experiments have been performed using radioactive sources that ionize differently than the cosmic rays which are responsible for the majority of atmospheric ionization. Here we report on an experimental study of sulphuric acid aerosol nucleation under near...... atmospheric conditions using a 580 MeV electron beam to ionize the volume of the reaction chamber. We find a clear and significant contribution from ion induced nucleation and consider this to be an unambiguous observation of the ion-effect on aerosol nucleation using a particle beam under conditions not far...

  19. Interpretation of aerosol trace metal particle size distributions

    International Nuclear Information System (INIS)

    Proton-induced X-ray emission (PIXE) analysis is capable of rapid routine determination of 10--15 elements present in amounts greater than or equal to 1 ng simultaneously in aerosol size fractions as collected by single orifice impactors over short periods of time. This enables detailed study of complex relationships between elements detected. Since absolute elemental concentrations may be strongly influenced by meteorological and topographical conditions, it is useful to normalize to a reference element. Comparison between the ratios of concentrations with aerosol and corresponding values for anticipated sources may lead to the identification of important sources for the elements. Further geochemical insights may be found through linear correlation coefficients, regression analysis, and cluster analysis. By calculating correlations for elemental pairs, an indication of the degree of covariance between the elements is obtained. Preliminary results indicate that correlations may be particle size dependent. A high degree of covariance may be caused either by a common source or may only reflect the conservative nature of the aerosol. In a regression analysis, by plotting elemental pairs and estimating the regression coefficients, we may be able to conclude if there is more than one source operating for a given element in a certain size range. Analysis of clustering of several elements, previously investigated for aerosol filter samples, can be applied to the analysis of aerosol size fractions. Careful statistical treatment of elemental concentrations as a function of aerosol particle size may thus yield significant information on the generation, transport and deposition of trace metals in the atmosphere

  20. Field Observations of the Processing of Organic Aerosol Particles and Trace Gases by Fogs and Clouds

    Science.gov (United States)

    Collett, J. L.; Herckes, P.

    2003-12-01

    In many environments, organic compounds account for a significant fraction of fine particle mass. Because the lifetimes of accumulation mode aerosol particles are governed largely by interactions with clouds, it is important to understand how organic aerosol particles are processed by clouds and fogs. Recently we have examined the organic composition of clouds and fogs in a variety of environments as well as how these fogs and clouds process organic aerosol particles and soluble organic trace gases. The investigations, conducted in Europe, North America, Central America, and the Pacific region, have included studies of polluted radiation fogs, orographic clouds in clean and polluted environments, and marine stratocumulus. Our results show that organic matter is a significant component of fog and cloud droplets. In polluted California radiation fogs, we observed concentrations of total organic carbon (TOC) ranging from 2 to 40 ppmC, with significantly lower concentrations measured in marine and continental clouds. An average of approximately 80 percent of organic matter was found in solution, while the remainder appears to be suspended material inside cloud and fog drops. Ultrafiltration measurements indicate that as much as half of the dissolved organic carbon is present in very large molecules with molecular weights in excess of 500 Daltons. Field measurements made using a two-stage cloud water collector reveal that organic matter tends to be enriched in smaller cloud or fog droplets. Consequently, removal of organic compounds by precipitating clouds or by direct cloud/fog drop deposition will be slowed due to the fact that small drops are incorporated less efficiently into precipitation and removed less efficiently by sedimentation or inertial impaction. Despite this trend, we have observed that sedimentation of droplets from long-lived radiation fogs provides a very effective mechanism for cleansing the atmosphere of carbonaceous aerosol particles, with organic

  1. Single particle characterization using the soot particle aerosol mass spectrometer (SP-AMS

    Directory of Open Access Journals (Sweden)

    A. K. Y. Lee

    2014-06-01

    Full Text Available Understanding the impact of atmospheric black carbon (BC containing particles on human health and radiative forcing requires knowledge of the mixing state of BC, including the characteristics of the materials with which it is internally mixed. In this study, we demonstrate for the first time the capabilities of the Aerodyne Soot-Particle Aerosol Mass Spectrometer equipped with a light scattering module (LS-SP-AMS to examine the mixing state of refractory BC (rBC and other aerosol components in an urban environment (downtown Toronto. K-means clustering analysis was used to classify single particle mass spectra into chemically distinct groups. One resultant cluster is dominated by rBC mass spectral signals (C1+ to C5+ while the organic signals fall into a few major clusters, identified as hydrocarbon-like organic aerosol (HOA, oxygenated organic aerosol (OOA, and cooking emission organic aerosol (COA. A nearly external mixing is observed with small BC particles only thinly coated by HOA (∼28% by mass on average, while over 90% of the HOA-rich particles did not contain detectable amounts of rBC. Most of the particles classified into other inorganic and organic clusters were not significantly associated with BC. The single particle results also suggest that HOA and COA emitted from anthropogenic sources were likely major contributors to organic-rich particles with low to mid-range aerodynamic diameter (dva. The similar temporal profiles and mass spectral features of the organic clusters and the factors from a positive matrix factorization (PMF analysis of the ensemble aerosol dataset validate the conventional interpretation of the PMF results.

  2. Characteristics and major sources of carbonaceous aerosols in PM{sub 2.5} from Sanya, China

    Energy Technology Data Exchange (ETDEWEB)

    Wang, Jingzhi [Key Lab of Aerosol Chemistry & Physics, Institute of Earth Environment, Chinese Academy of Sciences, Xi' an (China); State Key Lab of Loess and Quaternary Geology (SKLLQG), Institute of Earth Environment, Chinese Academy of Sciences, Xi' an (China); Ho, Steven Sai Hang [Key Lab of Aerosol Chemistry & Physics, Institute of Earth Environment, Chinese Academy of Sciences, Xi' an (China); Division of Atmospheric Sciences, Desert Research Institute, Reno, NV (United States); Cao, Junji, E-mail: cao@loess.llqg.ac.cn [Key Lab of Aerosol Chemistry & Physics, Institute of Earth Environment, Chinese Academy of Sciences, Xi' an (China); State Key Lab of Loess and Quaternary Geology (SKLLQG), Institute of Earth Environment, Chinese Academy of Sciences, Xi' an (China); Institute of Global Environmental Change, Xi' an Jiaotong University, Xi' an (China); Huang, Rujin [Key Lab of Aerosol Chemistry & Physics, Institute of Earth Environment, Chinese Academy of Sciences, Xi' an (China); State Key Lab of Loess and Quaternary Geology (SKLLQG), Institute of Earth Environment, Chinese Academy of Sciences, Xi' an (China); Laboratory of Atmospheric Chemistry, Paul Scherrer Institute (PSI), 5232 Villigen (Switzerland); Zhou, Jiamao [Key Lab of Aerosol Chemistry & Physics, Institute of Earth Environment, Chinese Academy of Sciences, Xi' an (China); State Key Lab of Loess and Quaternary Geology (SKLLQG), Institute of Earth Environment, Chinese Academy of Sciences, Xi' an (China); Zhao, Youzhi [College of Science and Technology, Qiongzhou University, Sanya (China); Xu, Hongmei [Department of Environmntal Science and Engineering, Xi' an Jiaotong University, Xi' an (China); Liu, Suixin; Wang, Gehui [Key Lab of Aerosol Chemistry & Physics, Institute of Earth Environment, Chinese Academy of Sciences, Xi' an (China); State Key Lab of Loess and Quaternary Geology (SKLLQG), Institute of Earth Environment, Chinese Academy of Sciences, Xi' an (China); and others

    2015-10-15

    PM{sub 2.5} samples were collected in Sanya, China in summer and winter in 2012/2013. Organic carbon (OC), elemental carbon (EC), and non-polar organic compounds including n-alkanes (n-C{sub 14}-n-C{sub 40}) and polycyclic aromatic hydrocarbons (PAHs) were quantified. The concentrations of these carbonaceous matters were generally higher in winter than summer. The estimated secondary organic carbon (OC{sub sec}) accounted for 38% and 54% of the total organic carbon (TOC) in winter and summer, respectively. The higher value of OC{sub sec} in addition to the presences of photochemically-produced PAHs in summer supports that photochemical conversions of organics are much active at the higher air temperatures and with stronger intense solar radiation. Carbon preference index (CPI) and percent contribution of wax n-alkanes suggest that anthropogenic sources were more dominant than derivation from terrestrial plants in Sanya. Diagnostic ratios of atmospheric PAHs further indicate that there was a wide mix of pollution sources in winter while fossil fuel combustion was the most dominant in summer. Positive Matrix Factorization (PMF) analysis with 18 PAHs in the winter samples found that motor vehicle emissions and biomass burning were the two main pollution sources, contributing 37.5% and 24.6% of the total quantified PAHs, respectively. - Highlights: • The first comprehensive study to investigate carbonaceous PM{sub 2.5} in Sanya, China • Higher carbonaceous levels in winter while more SOC formation in summer • Anthropogenic emission is the dominant sources of n-alkanes • Vehicle emission and biomass burning contributed ≥60% of the total PAHs in winter • The result supports better air quality in Sanya than most megacities in China.

  3. Tracing of aerosol sources in an urban environment using carbonaceous, major ions, Sr isotope, and mineralogical compositional data

    OpenAIRE

    Paula, A; S. Lopes; Ribeiro, S.; Santos, J. F.; Patinha, C.; Silva, E. A. Ferreira da; Soares, R.; Duarte, R.; A. Duarte

    2015-01-01

    Understanding the chemical composition of atmospheric particulate matter (PM), particularly with a diameter less than 2.5 μm (PM2.5), has became an emergent topic in atmospheric research due to its relation to climate change and serious health issues. In this study, a comprehensive assessment of the carbonaceous (organic carbon, water-soluble organic carbon, elemental carbon), major water-soluble inorganic ions (SO42-, NO3-, NH4+, Cl-, K+, Na+), 86Sr/87Sr isotope ratios, and mineralogical com...

  4. Fluorescence lifetime imaging of optically levitated aerosol: a technique to quantitatively map the viscosity of suspended aerosol particles.

    Science.gov (United States)

    Fitzgerald, C; Hosny, N A; Tong, H; Seville, P C; Gallimore, P J; Davidson, N M; Athanasiadis, A; Botchway, S W; Ward, A D; Kalberer, M; Kuimova, M K; Pope, F D

    2016-08-21

    We describe a technique to measure the viscosity of stably levitated single micron-sized aerosol particles. Particle levitation allows the aerosol phase to be probed in the absence of potentially artefact-causing surfaces. To achieve this feat, we combined two laser based techniques: optical trapping for aerosol particle levitation, using a counter-propagating laser beam configuration, and fluorescent lifetime imaging microscopy (FLIM) of molecular rotors for the measurement of viscosity within the particle. Unlike other techniques used to measure aerosol particle viscosity, this allows for the non-destructive probing of viscosity of aerosol particles without interference from surfaces. The well-described viscosity of sucrose aerosol, under a range of relative humidity conditions, is used to validate the technique. Furthermore we investigate a pharmaceutically-relevant mixture of sodium chloride and salbutamol sulphate under humidities representative of in vivo drug inhalation. Finally, we provide a methodology for incorporating molecular rotors into already levitated particles, thereby making the FLIM/optical trapping technique applicable to real world aerosol systems, such as atmospheric aerosols and those generated by pharmaceutical inhalers. PMID:27430158

  5. Fossil and non-fossil source contributions to atmospheric carbonaceous aerosols during extreme spring grassland fires in Eastern Europe

    OpenAIRE

    Ulevicius, Vidmantas; Byčenkienė, Steigvilė; Bozzetti, Carlo; Vlachou, Athanasia; Plauškaitė, Kristina; Mordas, Genrik; Dudoitis, Vadimas; Abbaszade, Gülcin; Remeikis, Vidmantas; Garbaras, Andrius; Masalaite, Agne; Blees, Jan; Fröhlich, Roman; Dällenbach, Kaspar R.; Canonaco, Francesco

    2016-01-01

    In early spring the Baltic region is frequently affected by high-pollution events due to biomass burning in that area. Here we present a comprehensive study to investigate the impact of biomass/grass burning (BB) on the evolution and composition of aerosol in Preila, Lithuania, during springtime open fires. Non-refractory submicron particulate matter (NR-PM1) was measured by an Aerodyne aerosol chemical speciation monitor (ACSM) and a source apportionment with the multilinea...

  6. Emission characteristics of carbonaceous particles and trace gases from open burning of crop residues in China

    Science.gov (United States)

    Ni, Haiyan; Han, Yongming; Cao, Junji; Chen, L.-W. Antony; Tian, Jie; Wang, Xiaoliang; Chow, Judith C.; Watson, John G.; Wang, Qiyuan; Wang, Ping; Li, Hua; Huang, Ru-Jin

    2015-12-01

    Open burning of crop residue is an important source of carbonaceous pollutants, and has a large impact on the regional environment and global climate change. Laboratory burn tests were conducted using a custom-made combustion chamber to determine pollutants (i.e. CO2, CO, PM2.5, organic carbon (OC) and elemental carbon (EC)) emission factors (EFs) of wheat straw, rice straw and corn stalk; the three major agricultural crop residues in China. The average EFs were estimated to be 1351 ± 147 g kg-1 for CO2, 52.0 ± 18.9 g kg-1 for CO, 10.6 ± 5.6 g kg-1 for PM2.5, 4.8 ± 3.1 g kg-1 for OC and 0.24 ± 0.12 g kg-1 for EC. In addition, the effect of fuel moisture was investigated through the controlled burning of wheat straw. Increasing the moisture content decreased the CO2 EF, and increased the EFs of CO, PM2.5 and OC. Based on measurements from this study and nationwide statistics in crop type and area, pollutants emission inventories for crop residue combustion with 1° × 1° resolution were compiled for 2008. Total emissions were 120 Tg CO2, 4.6 Tg CO, 0.88 Tg PM2.5, 0.39 Tg OC and 0.02 Tg EC.

  7. Tracking Water Diffusion Fronts in a Highly Viscous Aerosol Particle

    Science.gov (United States)

    Bastelberger, Sandra; Krieger, Ulrich; Peter, Thomas

    2016-04-01

    Field measurements indicate that atmospheric secondary aerosol particles can be present in a highly viscous, glassy state [1]. In contrast to liquid state particles, the gas phase equilibration is kinetically limited and governed by condensed phase diffusion. In recent water diffusion experiments on highly viscous single aerosol particles levitated in an electrodynamic balance (EDB) we observed a characteristic shift behavior of the Mie whispering gallery modes (WGM) indicative of the changing radial structure of the particle, thus providing us with an experimental method to track the diffusion process inside the particle. When a highly viscous, homogeneous particle is exposed to an abrupt increase in relative humidity, the rapid gas phase diffusion and strong concentration dependence of the diffusion coefficient in the condensed phase lead to extremely steep water concentration gradients inside the particle, reminiscent of diffusion fronts. The resulting quasi step-like concentration profile motivates the introduction of a simple core-shell model describing the morphology of the non-equilibrium particle during humidification. The subsequent particle growth and reduction of the shell refractive index can be observed as red and blueshift behavior of the WGM, respectively. The shift pattern can be attributed to a core-shell radius ratio and particle radius derived from model calculations [2]. If supplemented with growth information obtained from the WGM redshift and thermodynamic equilibrium data, we can infer a comprehensive picture of the time evolution of the diffusion fronts in the framework of our core-shell model. The measured time dependent concentration profile is then compared with simulations solving the non-linear diffusion equation [3] [1] Virtanen, A., et al., Nature, 467, 824-827, 2010 [2] Kaiser, T., Schweiger, G., Computers in Physics, Vol. 7, No. 6, 682-686, Nov/Dec 1993 [3] Zobrist, B., Soonsin, V., Luo, B.P., Peter, T. et al., Phys. Chem. Chem

  8. Aerosol dynamics and the synthesis of fine solid particles

    Energy Technology Data Exchange (ETDEWEB)

    Bandyopadhyaya, R.; Lall, A.A.; Friedlander, S.K. [University of California in Los Angeles, Los Angeles, CA (USA). Dept. of Chemical Engineering

    2004-01-26

    Aerosol dynamics (AD) is the discipline that deals with changes in particle size distributions in space and time. AD is based on (1) certain fundamental principles embodied in a set of equations, (2) experimental methods and instrumentation and (3) numerical and computational methods. Over the last few decades, AD has emerged as an enabling discipline in the design of aerosol reactors employed in the gas phase synthesis of fine powders, the characterization of particle emissions from sources such as coal-fired power plants and the atmospheric aerosol. The development of basic AD concepts since early in the 20th century is traced to the present. Major gaps that remain in the field and likely advances over the next few years are discussed. Although accurate predictions of particle size from first principles are difficult to make in practical applications, AD principles can be used to explain trends in product properties for flame and laser ablation reactors that operate under very different temperatures and quench rates.

  9. The rate of equilibration of viscous aerosol particles

    Science.gov (United States)

    O'Meara, Simon; Topping, David O.; McFiggans, Gordon

    2016-04-01

    The proximity of atmospheric aerosol particles to equilibrium with their surrounding condensable vapours can substantially impact their transformations, fate and impacts and is the subject of vibrant research activity. In this study we first compare equilibration timescales estimated by three different models for diffusion through aerosol particles to assess any sensitivity to choice of model framework. Equilibration times for diffusion coefficients with varying dependencies on composition are compared for the first time. We show that even under large changes in the saturation ratio of a semi-volatile component (es) of 1-90 % predicted equilibration timescales are in agreement, including when diffusion coefficients vary with composition. For condensing water and a diffusion coefficient dependent on composition, a plasticising effect is observed, leading to a decreased estimated equilibration time with increasing final es. Above 60 % final es maximum equilibration times of around 1 s are estimated for comparatively large particles (10 µm) containing a relatively low diffusivity component (1 × 10-25 m2 s-1 in pure form). This, as well as other results here, questions whether particle-phase diffusion through water-soluble particles can limit hygroscopic growth in the ambient atmosphere. In the second part of this study, we explore sensitivities associated with the use of particle radius measurements to infer diffusion coefficient dependencies on composition using a diffusion model. Given quantified similarities between models used in this study, our results confirm considerations that must be taken into account when designing such experiments. Although quantitative agreement of equilibration timescales between models is found, further work is necessary to determine their suitability for assessing atmospheric impacts, such as their inclusion in polydisperse aerosol simulations.

  10. Quantification of aerosol chemical composition using continuous single particle measurements

    OpenAIRE

    C.-H. Jeong; M. L. McGuire; K. J. Godri; Slowik, J. G.; P. J. G. Rehbein; G. J. Evans

    2011-01-01

    Mass concentrations of sulphate, nitrate, ammonium, organic carbon (OC), elemental carbon (EC) were determined from real time single particle data in the size range 0.1–3.0 μm measured by an Aerosol Time-of-Flight Mass Spectrometer (ATOFMS) at urban and rural sites in Canada. To quantify chemical species within individual particles measured by an ATOFMS, ion peak intensity of m/z −97 for sulphate, −62 for nitrate, +18 for ammonium, +43 for OC, and +36 for EC were scaled usi...

  11. Quantification of aerosol chemical composition using continuous single particle measurements

    OpenAIRE

    Jeong, C.-H.; M. L. McGuire; K. J. Godri; Slowik, J. G.; P. J. G. Rehbein; G. J. Evans

    2011-01-01

    Mass concentrations of sulphate, nitrate, ammonium, organic carbon (OC), elemental carbon (EC) were determined from real time single particle data in the size range 0.1–3.0 μm measured by an Aerosol Time-of-Flight Mass Spectrometer (ATOFMS) at urban and rural sites in Canada. To quantify chemical species within individual particles measured by an ATOFMS, ion peak intensity of m/z −97 for sulphate, −62 for nitrate, +18 for ammonium, +43 for OC, and +36 for EC were scaled usin...

  12. Optical particle counter measurement of marine aerosol hygroscopic growth

    Directory of Open Access Journals (Sweden)

    J. R. Snider

    2007-08-01

    Full Text Available A technique is developed for the determination of the hygroscopic growth factor of dry particles with diameter between 0.3 and 0.6 µm and is applied to measurements made during the second Dynamics and Chemistry of Marine Stratocumulus experiment. Two optical particle counters are utilized, one measures the aerosol size spectrum at ambient relative humidity and the other simultaneously dries the aerosol prior to light scattering detection. Growth factors are based on measurements made in the region of the Mie scattering curve where scattered light intensity increases monotonically with dry and wet particle diameter, i.e. D<0.9 µm. Factors influencing the accuracy of the measurement are evaluated, including particle drying, refractive index and shape. Growth factors at 90±3% ambient relative humidity in marine airmasses 400 km west of San Diego, California range between 1.5 and 1.8. This suggests that a significant fraction of the particle mass, between 40 and 70%, is either non-hygroscopic or weakly hygroscopic.

  13. Optical particle counter measurement of marine aerosol hygroscopic growth

    Directory of Open Access Journals (Sweden)

    J. R. Snider

    2008-04-01

    Full Text Available A technique is developed for the determination of the hygroscopic growth factor of dry particles with diameter between 0.3 and 0.6 μm and is applied to measurements made during the second Dynamics and Chemistry of Marine Stratocumulus experiment (DYCOMS-II. Two optical particle counters are utilized, one measures the aerosol size spectrum at ambient relative humidity and the other simultaneously dries the aerosol prior to light scattering detection. Growth factors are based on measurements made in the region of the Mie scattering curve where scattered light intensity increases monotonically with dry and wet particle diameter, i.e. D<0.9 μm. Factors influencing the accuracy of the measurement are evaluated, including particle drying, refractive index and shape. Growth factors at 90±3% ambient relative humidity in marine airmasses 400 km west of San Diego, California range between 1.5 and 1.8. This suggests that a significant fraction of the particle mass, between 40 and 70%, is either non-hygroscopic or weakly hygroscopic.

  14. Evaluation of a global aerosol microphysics model against size-resolved particle statistics in the marine atmosphere

    Directory of Open Access Journals (Sweden)

    D. V. Spracklen

    2007-01-01

    Full Text Available A statistical synthesis of marine aerosol measurements from experiments in four different oceans is used to evaluate a global aerosol microphysics model (GLOMAP. We compare the model against observed size resolved particle concentrations, probability distributions, and the temporal persistence of different size particles. We attempt to explain the observed sub-micrometre size distributions in terms of sulfate and sea spray and quantify the possible contributions of anthropogenic sulfate and carbonaceous material to the number and mass distribution. The model predicts a bimodal size distribution that agrees well with observations as a grand average over all regions, but there are large regional differences. Notably, observed Aitken mode number concentrations are more than a factor 10 higher than in the model for the N Atlantic but a factor 7 lower than the model in the NW Pacific. We also find that modelled Aitken mode and accumulation mode geometric mean diameters are generally smaller in the model by 10–30%. Comparison with observed free tropospheric Aitken mode distributions suggests that the model underpredicts growth of these particles during descent to the marine boundary layer (MBL. Recent observations of a substantial organic component of free tropospheric aerosol could explain this discrepancy. We find that anthropogenic continental material makes a substantial contribution to N Atlantic MBL aerosol, with typically 60–90% of sulfate across the particle size range coming from anthropogenic sources, even if we analyse air that has spent an average of >120 h away from land. However, anthropogenic primary black carbon and organic carbon particles (at the emission size and quantity assumed here do not explain the large discrepancies in Aitken mode number. Several explanations for the discrepancy are suggested. The lack of lower atmospheric particle formation in the model may explain low N Atlantic particle concentrations. However, the

  15. Deposition of Aerosol Particles in Electrically Charged Membrane Filters

    International Nuclear Information System (INIS)

    A theory for the influence of electric charge on particle deposition on the surface of charged filters has been developed. It has been tested experimentally on ordinary membrane filters and Nuclepore filters of 8 μm pore size, with a bipolar monodisperse test aerosol of 1 μm particle diameter, and at a filter charge up to 20 μC/m2. Agreement with theory was obtained for the Coulomb force between filter and particle for both kinds of filters. The image force between charged filter and neutral particles did not result in the predicted deposition in the ordinary membrane filter, probably due to lacking correspondence between the filter model employed for the theory, and the real filter. For the Nuclepore filter a satisfactory agreement with theory was obtained, also at image interaction

  16. Radiocarbon-insights into temporal variations in the sources and concentrations of carbonaceous aerosols in the Los Angeles and Salt Lake City Metropolitan Areas

    Science.gov (United States)

    Czimczik, Claudia; Mouteva, Gergana; Simon, Fahrni; Guaciara, Santos; James, Randerson

    2014-05-01

    Increased fossil fuel consumption and biomass burning are contributing to significantly larger emissions of black carbon (BC) aerosols to the atmosphere. Together with organic carbon (OC), BC is a major constituent of fine particulate matter in urban air, contributes to haze and has been linked to a broad array of adverse health effects. Black carbon's high light absorption capacity and role in key (in-)direct climate feedbacks also lead to a range of impacts in the Earth system (e.g. warming, accelerated snow melt, changes in cloud formation). Recent work suggests that regulating BC emissions can play an important role in improving regional air quality and reducing future climate warming. However, BC's atmospheric transport pathways, lifetime and magnitudes of emissions by sector and region, particularly emissions from large urban centers, remain poorly constrained by measurements. Contributions of fossil and modern sources to the carbonaceous aerosol pool (corresponding mainly to traffic/industrial and biomass-burning/biogenic sources, respectively) can be quantified unambiguously by measuring the aerosol radiocarbon (14C) content. However, accurate 14C-based source apportionment requires the physical isolation of BC and OC, and minimal sample contamination with extraneous carbon or from OC charring. Compound class-specific 14C analysis of BC remains challenging due to very small sample sizes (5-15 ug C). Therefore, most studies to date have only analyzed the 14C content of the total organic carbonaceous aerosol fraction. Here, we present time-series 14C data of BC and OC from the Los Angeles (LA) metropolitan area in California - one of two megacities in the United States - and from Salt Lake City (SLC), UT. In the LA area, we analyzed 48h-PM10 samples near the LA port throughout 2007 and 2008 (with the exception of summer). We also collected monthly-PM2.5 samples at the University of California - Irvine, with shorter sampling periods during regional wildfire

  17. Effects of particle shape, hematite content and semi-external mixing with carbonaceous components on the optical properties of accumulation mode mineral dust

    Directory of Open Access Journals (Sweden)

    S. K. Mishra

    2010-12-01

    Full Text Available The radiative forcing estimation of the polluted mineral dust is limited due to lack of morphological analysis, mixing state with the carbonaceous components and the hematite content in the pure dust. The accumulation mode mineral dust has been found to mix with anthropogenically produced black carbon, organic carbon and brown carbon during long range transport. The above features of the polluted dust are not well accounted in the optical models and lead the uncertainty in the numerical estimation of their radiative impact. The Semi-external mixing being a prominent mixing of dust and carbonaceous components has not been studied in details so for compared to core-shell, internal and external mixing studies. In present study, we consider the pure mineral dust composed of non-metallic components (such as Quartz, Feldspar, Mica and Calcite and metalic component like hematite (Fe2O3. The hematite percentage in the pure mineral dust governs its absorbance. Based on this hematite variation, the hematite fraction in pure mineral dust has been constrained between 0–8%. The morphological and mineralogical characterization of the polluted dust led to consider the three sphere, two sphere and two spheroid model shapes for polluted dust particle system. The pollution gives rise to various light absorbing aerosol components like black carbon, brown carbon and organic carbon (comprising of HUmic-Like Substances, HULIS in the atmosphere. The entire above discussed model shapes have been considered for the mineral dust getting polluted with (1 organic carbon (especially HULIS component (2 Brown carbon and (3 black carbon by making a semi-external mixture with pure mineral dust. The optical properties (like Single Scattering Albedo, SSA; Asymmetry parameter, g and Extinction efficiency, Qext of above model shapes for the polluted dust have been computed using Discrete Dipole Approximation, DDA code. For above

  18. Oxalate metal complexes in aerosol particles: implications for the hygroscopicity of oxalate-containing particles

    Directory of Open Access Journals (Sweden)

    T. Furukawa

    2011-05-01

    Full Text Available Atmospheric aerosols have both a direct and an indirect cooling effect that influences the radiative balance at the Earth's surface. It has been estimated that the degree of cooling is large enough to weaken the warming effect of carbon dioxide. Among the cooling factors, secondary organic aerosols (SOA play an important role in the solar radiation balance in the troposphere as SOA can act as cloud condensation nuclei (CCN and extend the lifespan of clouds because of their high hygroscopic and water soluble nature. Oxalic acid is an important component of SOA, and is produced via several formation pathways in the atmosphere. However, it is not certain whether oxalic acid exists as free oxalic acid or as metal oxalate complexes in aerosols, although there is a marked difference in their solubility in water and their hygroscopicity. We employed X-ray absorption fine structure spectroscopy to characterize the calcium (Ca and zinc (Zn in aerosols collected at Tsukuba in Japan. Size-fractionated aerosol samples were collected for this purpose using an impactor aerosol sampler. It was shown that 10–60% and 20–100% of the total Ca and Zn in the finer particles (<2.1 μm were present as Ca and Zn oxalate complexes, respectively. Oxalic acid is hygroscopic and can thus increase the CCN activity of aerosol particles, while complexes with various polyvalent metal ions such as Ca and Zn are not hygroscopic, which cannot contribute to the increase of the CCN activity of aerosols. Based on the concentrations of noncomplexed and metal-complexed oxalate species, we found that most of the oxalic acid is present as metal oxalate complexes in the aerosols, suggesting that oxalic acid does not always increase the hygroscopicity of aerosols in the atmosphere. Similar results are expected for other dicarboxylic acids, such as malonic and succinic acids. Thus, it is advisable that the cooling effect of organic aerosols should be estimated by including the

  19. Fossil vs. non-fossil sources of fine carbonaceous aerosols in four Chinese cities during the extreme winter haze episode of 2013

    Science.gov (United States)

    Zhang, Y.-L.; Huang, R.-J.; El Haddad, I.; Ho, K.-F.; Cao, J.-J.; Han, Y.; Zotter, P.; Bozzetti, C.; Daellenbach, K. R.; Canonaco, F.; Slowik, J. G.; Salazar, G.; Schwikowski, M.; Schnelle-Kreis, J.; Abbaszade, G.; Zimmermann, R.; Baltensperger, U.; Prévôt, A. S. H.; Szidat, S.

    2015-02-01

    During winter 2013, extremely high concentrations (i.e., 4-20 times higher than the World Health Organization guideline) of PM2.5 (particulate matter with an aerodynamic diameter coal combustion and vehicle exhaust dominated EC with a mean contribution of 75 ± 8% across all sites. The remaining 25 ± 8% was exclusively attributed to biomass combustion, consistent with the measurements of biomass-burning markers such as anhydrosugars (levoglucosan and mannosan) and water-soluble potassium (K+). With a combination of the levoglucosan-to-mannosan and levoglucosan-to-K+ ratios, the major source of biomass burning in winter in China is suggested to be combustion of crop residues. The contribution of fossil sources to OC was highest in Beijing (58 ± 5%) and decreased from Shanghai (49 ± 2%) to Xi'an (38 ± 3%) and Guangzhou (35 ± 7%). Generally, a larger fraction of fossil OC was from secondary origins than primary sources for all sites. Non-fossil sources accounted on average for 55 ± 10 and 48 ± 9% of OC and total carbon (TC), respectively, which suggests that non-fossil emissions were very important contributors of urban carbonaceous aerosols in China. The primary biomass-burning emissions accounted for 40 ± 8, 48 ± 18, 53 ± 4 and 65 ± 26% of non-fossil OC for Xi'an, Beijing, Shanghai and Guangzhou, respectively. Other non-fossil sources excluding primary biomass burning were mainly attributed to formation of secondary organic carbon (SOC) from non-fossil precursors such as biomass-burning emissions. For each site, we also compared samples from moderately to heavily polluted days according to particulate matter mass. Despite a significant increase of the absolute mass concentrations of primary emissions from both fossil and non-fossil sources during the heavily polluted events, their relative contribution to TC was even decreased, whereas the portion of SOC was consistently increased at all sites. This observation indicates that SOC was an important fraction

  20. Influence of sampling artefacts on measured PM, OC, and EC levels in carbonaceous aerosols in an urban area

    Czech Academy of Sciences Publication Activity Database

    Viana, M.; Chi, X.; Maenhaut, W.; Cafmeyer, J.; Querol, X.; Alastuey, A.; Mikuška, Pavel; Večeřa, Zbyněk

    2006-01-01

    Roč. 40, č. 2 (2006), s. 107-117. ISSN 0278-6826 Institutional research plan: CEZ:AV0Z40310501 Keywords : sampling artefacts * OC/EC * urban aerosols Subject RIV: CB - Analytical Chemistry, Separation Impact factor: 2.905, year: 2006

  1. SPM analysis on groups of single aerosol particles around steel plant

    International Nuclear Information System (INIS)

    Several methods for preparing samples of dispersed single aerosol particles used in scanning proton microprobe (SPM) analysis were tested. Many elements such as Al, Si, S, Cl, Ca, Ti, Cr, Mn, Fe, Ni, Cu and Zn in the groups of different single aerosol particles from the Capital Steel Plant area were analyzed by SPM. The distributions of elemental contents in the group of single particles were mapped with three dimensional contour and the isometric. A new approach to study the group of different single aerosol particles for air pollution is developed in the present work. The results are significant to assessing the environmental impact of the dispersed single aerosol particles

  2. The chemical composition of fine ambient aerosol particles in the Beijing area

    Science.gov (United States)

    Nekat, Bettina; van Pinxteren, Dominik; Iinuma, Yoshiteru; Gnauk, Thomas; Müller, Konrad; Herrmann, Hartmut

    2010-05-01

    The strong economical growth in China during the last few decades led to heavy air pollution caused by significantly increased particle emissions. The aerosol particles affect not only the regional air quality and visibility, but can also influence cloud formation processes and the radiative balance of the atmosphere by their optical and microphysical properties. The ability to act as Cloud Condensation Nuclei (CCN) is related to microphysical properties like the hygroscopic growth or the cloud droplet activation. The chemical composition of CCN plays an important role on these properties and varies strongly with the particle size and the time of day. Hygroscopic or surface active substances can increase the hygroscopicity and lower the surface tension of the particle liquid phase, respectively. The presence of such compounds may result in faster cloud droplet activation by faster water uptake. The DFG project HaChi (Haze in China) aimed at studying physical and chemical parameters of urban aerosol particles in the Beijing area in order to associate the chemical composition of aerosol particles with their ability to act as CCN. To this end, two measurement campaigns were performed at the Wuqing National Ordinary Meteorological Observing Station, which is a background site near Beijing. The winter campaign was realized in March 2009 and the summer campaign took place from mid July 2009 to mid August 2009. Fine particles with an aerodynamic diameter smaller than or equal 1 μm were continuously sampled for 24h over the two campaigns using a DIGITEL high volume sampler (DHA-80). The present contribution presents and discusses the results of the chemical characterization of the DIGITEL filters samples. The filters were analyzed for the mass concentration, inorganic ions and carbon sum parameters like elemental (EC), organic (OC) and water soluble organic carbon (WSOC). The WSOC fraction was further characterized for hygroscopic substances like low molecular

  3. Physicochemical Characterization of Capstone Depleted Uranium Aerosols I: Uranium Concentration in Aerosols as a Function of Time and Particle Size

    International Nuclear Information System (INIS)

    During the Capstone Depleted Uranium (DU) Aerosol Study, aerosols containing depleted uranium were produced inside unventilated armored vehicles (i.e., Abrams tanks and Bradley Fighting Vehicles) by perforation with large-caliber DU penetrators. These aerosols were collected and characterized, and the data were subsequently used to assess human health risks to personnel exposed to DU aerosols. The DU content of each aerosol sample was first quantified by radioanalytical methods, and selected samples, primarily those from the cyclone separator grit chambers, were analyzed radiochemically. Deposition occurred inside the vehicles as particles settled on interior surfaces. Settling rates of uranium from the aerosols were evaluated using filter cassette samples that collected aerosol as total mass over eight sequential time intervals. A moving filter was used to collect aerosol samples over time particularly within the first minute after the shot. The results demonstrate that the peak uranium concentration in the aerosol occurred in the first 10 s, and the concentration decreased in the Abrams tank shots to about 50% within 1 min and to less than 2% 30 min after perforation. In the Bradley vehicle, the initial (and maximum) uranium concentration was lower than those observed in the Abrams tank and decreased more slowly. Uranium mass concentrations in the aerosols as a function of particle size were evaluated using samples collected in the cyclone samplers, which collected aerosol continuously for 2 h post perforation. The percentages of uranium mass in the cyclone separator stages from the Abrams tank tests ranged from 38% to 72% and, in most cases, varied with particle size, typically with less uranium associated with the smaller particle sizes. Results with the Bradley vehicle ranged from 18% to 29% and were not specifically correlated with particle size

  4. Physicochemical characterization of Capstone depleted uranium aerosols I: uranium concentration in aerosols as a function of time and particle size.

    Science.gov (United States)

    Parkhurst, Mary Ann; Cheng, Yung Sung; Kenoyer, Judson L; Traub, Richard J

    2009-03-01

    During the Capstone Depleted Uranium (DU) Aerosol Study, aerosols containing DU were produced inside unventilated armored vehicles (i.e., Abrams tanks and Bradley Fighting Vehicles) by perforation with large-caliber DU penetrators. These aerosols were collected and characterized, and the data were subsequently used to assess human health risks to personnel exposed to DU aerosols. The DU content of each aerosol sample was first quantified by radioanalytical methods, and selected samples, primarily those from the cyclone separator grit chambers, were analyzed radiochemically. Deposition occurred inside the vehicles as particles settled on interior surfaces. Settling rates of uranium from the aerosols were evaluated using filter cassette samples that collected aerosol as total mass over eight sequential time intervals. A moving filter was used to collect aerosol samples over time, particularly within the first minute after a shot. The results demonstrate that the peak uranium concentration in the aerosol occurred in the first 10 s after perforation, and the concentration decreased in the Abrams tank shots to about 50% within 1 min and to less than 2% after 30 min. The initial and maximum uranium concentrations were lower in the Bradley vehicle than those observed in the Abrams tank, and the concentration levels decreased more slowly. Uranium mass concentrations in the aerosols as a function of particle size were evaluated using samples collected in a cyclone sampler, which collected aerosol continuously for 2 h after perforation. The percentages of uranium mass in the cyclone separator stages ranged from 38 to 72% for the Abrams tank with conventional armor. In most cases, it varied with particle size, typically with less uranium associated with the smaller particle sizes. Neither the Abrams tank with DU armor nor the Bradley vehicle results were specifically correlated with particle size and can best be represented by their average uranium mass concentrations of 65

  5. Quantification of aerosol chemical composition using continuous single particle measurements

    Directory of Open Access Journals (Sweden)

    C.-H. Jeong

    2011-07-01

    Full Text Available Mass concentrations of sulphate, nitrate, ammonium, organic carbon (OC, elemental carbon (EC were determined from real time single particle data in the size range 0.1–3.0 μm measured by an Aerosol Time-of-Flight Mass Spectrometer (ATOFMS at urban and rural sites in Canada. To quantify chemical species within individual particles measured by an ATOFMS, ion peak intensity of m/z −97 for sulphate, −62 for nitrate, +18 for ammonium, +43 for OC, and +36 for EC were scaled using the number and size distribution data by an Aerodynamic Particle Sizer (APS and a Fast Mobility Particle Sizer (FMPS. Hourly quantified chemical species from ATOFMS single-particle analysis were compared with collocated fine particulate matter (aerodynamic diameter < 2.5 μm, PM2.5 chemical composition measurements by an Aerosol Mass Spectrometer (AMS at a rural site, a Gas-Particle Ion Chromatograph (GPIC at an urban site, and a Sunset Lab field OCEC analyzer at both sites. The highest correlation was found for nitrate, with correlation coefficients (Pearson r of 0.89 (ATOFMS vs. GPIC and 0.85 (ATOFMS vs. AMS. ATOFMS mass calibration factors, determined for the urban site, were used to calculate mass concentrations of the major PM2.5 chemical components at the rural site near the US border in southern Ontario. Mass reconstruction using the ATOFMS mass calibration factors agreed very well with the PM2.5 mass concentrations measured by a Tapered Element Oscillating Microbalance (TEOM, r = 0.86 at the urban site and a light scattering monitor (DustTrak, r = 0.87 at the rural site. In the urban area nitrate was the largest contributor to PM2.5 mass in the winter, while organics and sulphate contributed ~64 % of the summer PM2.5 in the rural area, suggesting a strong influence of regional/trans-boundary pollution. The mass concentrations of five major species in ten size-resolved particle

  6. A New Electrospray Aerosol Generator with High Particle Transmission Efficiency.

    Science.gov (United States)

    Fu, Huijing; Patel, Anand C; Holtzman, Michael J; Chen, Da-Ren

    2011-01-01

    A new single-capillary electrospray (ES) aerosol generator has been developed for monodisperse particle production with maximal transmission efficiency. The new generator consists of both a spray chamber in a point-to-orifice-plate configuration and a charge reduction chamber that can hold up to 4 Nuclespot ionizers (Model P-2042, NRD Inc.). The 2 chambers are partitioned by an orifice plate. To optimize the particle transmission efficiency of the prototype, a systematic study was performed on the generator by varying the system setup and operation. Two key dimensions of the generator setup, the orifice diameter and the distance from the capillary tip to the orifice plate, were varied. Fluorescence analysis was applied to characterize the loss of ES-generated particles at different locations of the prototype. It was found that particle loss in the generator could be reduced by either increasing the orifice diameter or decreasing the distance between the capillary tip and the orifice plate. Increasing either the total radioactivity of the ionizers or the flowrate of the particle carrier gas also further decreased the particle loss in the system. The maximum particle transmission efficiency of 88.0% was obtained with the spray chamber fully opened to the charge reduction chamber, the capillary tip at the same level as the orifice plate, and 4 bipolar ionizers installed. PMID:22829715

  7. Comparison of Spheroidal Carbonaceous Particle Data with Modelled Atmospheric Black Carbon Concentration and Deposition and Air Mass Sources in Northern Europe, 1850–2010

    OpenAIRE

    Meri Ruppel; Lund, Marianne T.; Henrik Grythe; Rose, Neil L.; Jan Weckström; Atte Korhola

    2013-01-01

    Spheroidal carbonaceous particles (SCP) are a well-defined fraction of black carbon (BC), produced only by the incomplete combustion of fossil fuels such as coal and oil. Their past concentrations have been studied using environmental archives, but, additionally, historical trends of BC concentration and deposition can be estimated by modelling. These models are based on BC emission inventories, but actual measurements of BC concentration and deposition play an essential role in their evaluat...

  8. Aerosol Particle Sources Affecting the Swedish Air Quality at Urban and Rural Level.

    OpenAIRE

    Kristensson, Adam

    2005-01-01

    During the last decades anthropogenic aerosol particles have attracted much attention due to their adverse health effects and their influence of climate change, and in Sweden, there are mainly three aerosol sources that affect the air quality; domestic wood combustion, traffic, and long distance transport, which includes new particle formation. This work concerns the characterization of these sources and an estimate of how much they contribute to the aerosol particle number (ToN) and mass con...

  9. Morphology and Optical Properties of Mixed Aerosol Particles

    Science.gov (United States)

    Fard, Mehrnoush M.; Krieger, Ulrich; Rudich, Yinon; Marcolli, Claudia; Peter, Thomas

    2016-04-01

    Experiments and modeling studies have shown that deliquesced aerosols can exist not only as one-phase system containing organics, inorganic salts and water, but often as two-phase systems consisting of a predominantly organic and a predominantly inorganic aqueous phase (1,2). Recent laboratory studies conducted with model mixtures representing tropospheric aerosols (1,2,3), secondary organic aerosol (SOA) from smog chamber experiments (4), and field measurements (5) suggest that liquid-liquid phase separations (LLPS) is indeed a common phenomenon in mixed organic/ inorganic particles. During LLPS, particles may adopt different morphologies mainly core-shell and partially engulfed. A core-shell configuration will have consequences for heterogeneous chemistry and hygroscopicity and as a result will alter the optical properties of the particles in particular for organic phases containing absorbing molecules, e.g. brown carbon. The primary objective of this project is to establish a method for investigating the morphology of mixed inorganic and absorbing organic compounds of atmospheric relevance and study their radiative properties before, during, and after phase transitions mainly during LLPS. This will be the first study looking into the radiative effect of LLPS in detail. Our ternary model system consist of ammonium sulfate (AS)/ Polyethylene Glycol (PEG)/ and water (H2O). Carminic acid (CA) was added as a proxy for an absorbing organic compound to the system. The behavior of single droplets of above ternary mixture was monitored during relative humidity (RH) cycles using optical microscopy. The same ternary mixture particle was levitated in an electrodynamic balance (EDB) and the change in its absorption properties was measured at varying RH. In addition, Mie-code modeling is used to predict the absorption efficiency of the same ternary system and the result will be compared with the data obtained from EDB experiment. We also intend to determine the occurrence of

  10. Source apportionment and dynamic changes of carbonaceous aerosols during the haze bloom-decay process in China based on radiocarbon and organic molecular tracers

    Science.gov (United States)

    Liu, Junwen; Li, Jun; Liu, Di; Ding, Ping; Shen, Chengde; Mo, Yangzhi; Wang, Xinming; Luo, Chunling; Cheng, Zhineng; Szidat, Sönke; Zhang, Yanlin; Chen, Yingjun; Zhang, Gan

    2016-03-01

    Fine carbonaceous aerosols (CAs) is the key factor influencing the currently filthy air in megacities in China, yet few studies simultaneously focus on the origins of different CAs species using specific and powerful source tracers. Here, we present a detailed source apportionment for various CAs fractions, including organic carbon (OC), water-soluble OC (WSOC), water-insoluble OC (WIOC), elemental carbon (EC) and secondary OC (SOC) in the largest cities of North (Beijing, BJ) and South China (Guangzhou, GZ), using the measurements of radiocarbon and anhydrosugars. Results show that non-fossil fuel sources such as biomass burning and biogenic emission make a significant contribution to the total CAs in Chinese megacities: 56 ± 4 in BJ and 46 ± 5 % in GZ, respectively. The relative contributions of primary fossil carbon from coal and liquid petroleum combustions, primary non-fossil carbon and secondary organic carbon (SOC) to total carbon are 19, 28 and 54 % in BJ, and 40, 15 and 46 % in GZ, respectively. Non-fossil fuel sources account for 52 in BJ and 71 % in GZ of SOC, respectively. These results suggest that biomass burning has a greater influence on regional particulate air pollution in North China than in South China. We observed an unabridged haze bloom-decay process in South China, which illustrates that both primary and secondary matter from fossil sources played a key role in the blooming phase of the pollution episode, while haze phase is predominantly driven by fossil-derived secondary organic matter and nitrate.

  11. Development of Laser-Based Handheld Aerosol Particle Counter

    Institute of Scientific and Technical Information of China (English)

    CHEN Chang; LI Hui

    2005-01-01

    The JC-CA300 handheld Aerosol particle counter is designed and developed based on light scattering principle. The JC-CA300 counter is composed of optical sensor, DSP component and microprocessor unit. The hardware architecture is designed in compact style by SMT IC chips. The whole counter weight is less than 2 pounds. With 32K RAM space, the JC-CA300 can store 500 sampling records and support standard printer and communicate with a computer through RS232 interface. Based on experimental results, the main performance of JC-CA300 is better than that of the ARTI'S HHPC-6 instrument.

  12. Sulfur isotope analysis of aerosol particles by NanoSIMS

    OpenAIRE

    Winterholler, Bärbel

    2007-01-01

    A new method to measure the sulfur isotopic composition of individual aerosol particles by NanoSIMS has been developed and tested on several standards such as barite (BaSO4), anhydrite (CaSO4), gypsum (CaSO4·2H2O), mascagnite ((NH4)2SO4), epsomite (MgSO4·7H2O), magnesium sulfate (MgSO4·xH2O), thenardite (Na2SO4), boetite (K2SO4) and cysteine (an amino acid). This ion microprobe technique employs a Cs+ primary ion beam and measures negative secondary ions permitting the analysis of sulfur isot...

  13. Nature and evolution of ultrafine aerosol particles in the atmosphere

    Science.gov (United States)

    Smirnov, V. V.

    2006-12-01

    Results of experimental and theoretical studies of a poorly understood phenomenon, an intense emission of ultrafine (nanometer) aerosols (ENA), are reviewed. In the English-language literature, this phenomenon is commonly referred to as a nucleation burst. ENA events have been observed on all the continents and throughout the depth of the troposphere, with the number of corresponding publications growing steadily. Intense and long-lasting ENA events have been studied more or less comprehensively and in full detail for Northern Europe, with 60 to 70% of observations taken in a forest area in the presence of snow cover and 10 to 20% in coastal marine areas. Most often, ENA events occur during spring and fall, with 95% of cases in the daytime and under sunny calm conditions, typical of anticyclones. In ENA events, the concentration of nanoparticles initially grows rapidly to values of 103-105 cm-3. One or two hours later, the so-called nuclei fraction with diameters D = 3-15 nm is produced. The appearance of the Aitken fraction D = 20-80 nm and the enlargement of aerosol particles inside the accumulation fraction D = 80-200 nm may occur during the following 4-6 h. Thus, the cycle of formation and growth of atmospheric aerosol particles in the size range from a few to hundreds of nanometers is reproduced over 6-8 h. A specific synoptic feature of ENA events over land is that they occur when the polar air is transported to measuring sites and the temperature difference between day and light is large. During ENA periods, the formation rate of condensation nuclei with a diameter of 100 nm increases 10-to 100-fold. Important factors of ENA genesis are the “aerosol” and “electric” states of the atmosphere. More intense ENA events occur at low concentrations of background aerosols in the presence of atmospheric ions of medium mobility with D = 2-3 nm. The international experiments ACE 1 and 2, BIOFOR 1, 2, and 3, ESUP 2000, QUEST, etc., have not yet provided any

  14. Experimental Determination of Chemical Diffusion within Secondary Organic Aerosol Particles

    Energy Technology Data Exchange (ETDEWEB)

    Abramson, Evan H.; Imre, D.; Beranek, Josef; Wilson, Jacqueline; Zelenyuk, Alla

    2013-02-28

    Formation, properties, transformations, and temporal evolution of secondary organic aerosols (SOA) particles strongly depend on particle phase. Recent experimental evidence from a number of groups indicates that SOA is in a semi-solid phase, the viscosity of which remained unknown. We find that when SOA is made in the presence of vapors of volatile hydrophobic molecules the SOA particles absorb and trap them. Here, we illustrate that it is possible to measure the evaporation rate of these molecules that is determined by their diffusion in SOA, which is then used to calculate a reasonably accurate value for the SOA viscosity. We use pyrene as a tracer molecule and a-pinene SOA as an illustrative case. It takes ~24 hours for half the pyrene to evaporate to yield a viscosity of 10^8 Pa s for a-pinene. This viscosity is consistent with measurements of particle bounce and evaporation rates. We show that viscosity of 10^8 Pa s implies coalescence times of minutes, consistent with the findings that SOA particles are spherical. Similar measurements on aged SOA particles doped with pyrene yield a viscosity of 10^9 Pa s, indicating that hardening occurs with time, which is consistent with observed decrease in water uptake and evaporation rate with aging.

  15. Characterization of the geometrical properties of agglomerated aerosol particles

    International Nuclear Information System (INIS)

    A method for the absolute mass determination of agglomerated aerosol particles is presented. Based on this method it is possible to determine simultaneously and in situ mass, exposed surface and mobility diameter. From these measurements the fractal dimension of aerosol particles can be derived. For silver agglomerates produced by spark discharge it was found that they are bifractal. The fractal dimension was 3 in the free molecular regime and 1.9 in the transition regime. By variation of the gas mean free path it was shown that the region where the agglomerate structure changes from close-packed particle to low density agglomerates depends on the Knudsen number. In the free molecular regime the fractal dimension was not at all affected by any change of the generation conditions. Only sintering caused an increase in the density which was attributed to mass transport within the agglomerate. In the transition regime the fractal dimension remained constant with increasing monomer concentration and with increasing flow rate, but it increased with increasing pressure, increasing Ar:He ratio and with increasing sintering temperature. For sintering this effect was explained by the minimization of the surface free energy. It was found that the structure changing rate is proportional to the product of sintering temperature and residence time in the sintering oven. By carefully adjusting the temperature it is possible to produce agglomerates of a well defined structure. In desorption experiments of 136I from silver and carbon agglomerates it could be shown that the desorption behavior is different. It was found that the desorption enthalpy of iodine from graphite and silver particles were -142 kJ/mol and -184 kJ/mol, respectively. Moreover, it was demonstrated that the 136I attachment to particles is different for silver agglomerates with the same mobility, but different structures. (author) 41 figs., refs

  16. EVALUATION OF ACOUSTIC FORCES ON A PARTICLE IN AEROSOL MEDIUM

    Energy Technology Data Exchange (ETDEWEB)

    Lee, S; Richard Dimenna, R

    2007-09-27

    The acoustic force exerted on a solid particle was evaluated to develop a fundamental understanding of the critical physical parameters or constraints affecting particle motion and capture in a collecting device. The application of an acoustic force to the collection of a range of submicron-to-micron particles in a highly turbulent airflow stream laden with solid particles was evaluated in the presence of other assisting and competing forces. This scoping estimate was based on the primary acoustic force acting directly on particles in a dilute aerosol system, neglecting secondary interparticle effects such as agglomeration of the sub-micron particles. A simplified analysis assuming a stable acoustic equilibrium with an infinite sound speed in the solid shows that for a solid-laden air flow in the presence of a standing wave, particles will move toward the nearest node. The results also show that the turbulent drag force on a 1-{micro}m particle resulting from eddy motion is dominant when compared with the electrostatic force or the ultrasonic acoustic force. At least 180 dB acoustic pressure level at 1 MHz is required for the acoustic force to be comparable to the electrostatic or turbulent drag forces in a high-speed air stream. It is noted that particle size and pressure amplitude are dominant parameters for the acoustic force. When acoustic pressure level becomes very large, the acoustic energy will heat up the surrounding air medium, which may cause air to expand. With an acoustic power of about 600 watts applied to a 2000-lpm air flow, the air temperature can increase by as much as 15 C at the exit of the collector.

  17. Long-term measurements of carbonaceous aerosols in the Eastern Mediterranean: evidence of long-range transport of biomass burning

    Directory of Open Access Journals (Sweden)

    J. Sciare

    2008-09-01

    Full Text Available Long-term (5-year measurements of Elemental Carbon (EC and Organic Carbon (OC in bulk aerosols are presented here for the first time in the Mediterranean Basin (Crete Island. A multi-analytical approach (including thermal, optical, and thermo-optical techniques was applied for these EC and OC measurements. Light absorbing dust aerosols were shown to poorly contribute (+12% on a yearly average to light absorption coefficient (babs measurements performed by an optical method (aethalometer. Long-range transport of agricultural waste burning from European countries surrounding the Black Sea was shown for each year during two periods (March–April and July–September. The contribution of biomass burning to the concentrations of EC and OC was shown to be rather small (20 and 14%, respectively, on a yearly basis, although this contribution could be much higher on a monthly basis and showed important seasonal and interannual variability. By removing the biomass burning influence, our data revealed an important seasonal variation of OC, with an increase by almost a factor of two for the spring months of May and June, whereas BC was found to be quite stable throughout the year. Preliminary measurements of Water Soluble Organic Carbon (WSOC have shown that the monthly mean WSOC/OC ratio remains stable throughout the year (0.45±0.12, suggesting that the partitioning between water soluble and water insoluble organic matter is not significantly affected by biomass burning and secondary organic aerosol (SOA formation. A chemical mass closure performed in the fine mode (Aerodynamic Diameter, A.D.<1.5μm showed that the mass contribution of organic matter (POM was found to be essentially invariable during the year (monthly average of 26±5%.

  18. Long-term measurements of carbonaceous aerosols in the eastern Mediterranean: evidence of long-range transport of biomass burning

    Directory of Open Access Journals (Sweden)

    J. Sciare

    2008-04-01

    Full Text Available Long-term (5-yr measurements of Black Carbon (BC and Organic Carbon (OC in bulk aerosols are presented here for the first time in the Mediterranean Basin (Crete Island. A multi-analytical approach (including thermal, optical, and thermo-optical techniques was applied for these BC and OC measurements. Light absorbing dust aerosols have shown to poorly contribute (+17% on a yearly average to light absorption coefficient (babs measurements performed by an optical method (aethalometer. Long-range transport of agricultural waste burning from European countries surrounding the Black Sea was shown for each year during two periods (March–April and July–September. The contribution of biomass burning to the concentrations of BC and OC has shown to be rather small (20 and 14%, respectively, on a yearly basis, although this contribution could be much higher on a monthly basis and is expected a high intra and inter annual variability. By removing the biomass burning influence, our data revealed an important seasonal variation of OC, with an increase by almost a factor of two for the Spring months of May and June, whereas BC was found to be quite stable throughout the year. Preliminary measurements of Water Soluble Organic Carbon (WSOC have shown that the monthly mean WSOC/OC ratio remains stable throughout the year (0.45±0.12, suggesting that the partitioning between water soluble and water insoluble organic matter is not significantly affected by biomass burning and secondary organic aerosol (SOA formation. A chemical mass closure performed in the fine mode (Aerodynamic Diameter, A.D.<1.5 μm showed that the mass contribution of organic matter (POM was found to be essentially invariable during the year (monthly average of 26±5%.

  19. Long-term measurements of carbonaceous aerosols in the Eastern Mediterranean: evidence of long-range transport of biomass burning

    International Nuclear Information System (INIS)

    Long-term (5-year) measurements of Elemental Carbon (EC) and Organic Carbon (OC) in bulk aerosols are presented here for the first time in the Mediterranean Basin (Crete Island). A multi-analytical approach (including thermal, optical, and thermo-optical techniques) was applied for these EC and OC measurements. Light absorbing dust aerosols were shown to poorly contribute (+12% on a yearly average) to light absorption coefficient (b(abs)) measurements performed by an optical method (aethalometer). Long-range transport of agricultural waste burning from European countries surrounding the Black Sea was shown for each year during two periods (March-April and July-September). The contribution of biomass burning to the concentrations of EC and OC was shown to be rather small (20 and 14%, respectively, on a yearly basis), although this contribution could be much higher on a monthly basis and showed important seasonal and inter annual variability. By removing the biomass burning influence, our data revealed an important seasonal variation of OC, with an increase by almost a factor of two for the spring months of May and June, whereas BC was found to be quite stable throughout the year. Preliminary measurements of Water Soluble Organic Carbon (WSOC) have shown that the monthly mean WSOC/ OC ratio remains stable throughout the year (0.45 ± 0.12), suggesting that the partitioning between water soluble and water insoluble organic matter is not significantly affected by biomass burning and secondary organic aerosol (SOA) formation. A chemical mass closure performed in the fine mode (Aerodynamic Diameter, A. D.≤ 1.5 μm) showed that the mass contribution of organic matter (POM) was found to be essentially invariable during the year (monthly average of 26 ± 5%). (authors)

  20. A sample preparation method of individual aerosol particles in SPM analysis

    International Nuclear Information System (INIS)

    A new method for sample preparation of individual aerosol particle in SPM analysis was developed. Aerosol particles were collected directly on the polyvinyl butyral (PVB) foil by using air sampler. Microscopic observation indicates that the particles were separated completely and the interval of particles was reasonable. The SPM experiment proves that PVB foils have excellent stability under proton microbeam bombardment and are a suitable backing material for supporting the single particle for SPM analysis. (authors)

  1. Inverse problem for particle size distributions of atmospheric aerosols using stochastic particle swarm optimization

    International Nuclear Information System (INIS)

    As a part of resolving optical properties in atmosphere radiative transfer calculations, this paper focuses on obtaining aerosol optical thicknesses (AOTs) in the visible and near infrared wave band through indirect method by gleaning the values of aerosol particle size distribution parameters. Although various inverse techniques have been applied to obtain values for these parameters, we choose a stochastic particle swarm optimization (SPSO) algorithm to perform an inverse calculation. Computational performances of different inverse methods are investigated and the influence of swarm size on the inverse problem of computation particles is examined. Next, computational efficiencies of various particle size distributions and the influences of the measured errors on computational accuracy are compared. Finally, we recover particle size distributions for atmospheric aerosols over Beijing using the measured AOT data (at wavelengths λ=0.400, 0.690, 0.870, and 1.020 μm) obtained from AERONET at different times and then calculate other AOT values for this band based on the inverse results. With calculations agreeing with measured data, the SPSO algorithm shows good practicability.

  2. A new comprehensive approach to characterizing carbonaceous aerosol with an application to wintertime Fresno, California PM2.5

    Science.gov (United States)

    Herckes, P.; Leenheer, J.A.; Collett, J.L., Jr.

    2007-01-01

    Fine particulate matter (PM2.5) samples were collected during a three week winter period in Fresno (CA). A composite sample was characterized by isolating several distinct fractions and characterizing them by infrared and nuclear magnetic resonance (NMR) spectroscopy. More than 80% of the organic matter in the aerosol samples was recovered and characterized. Only 35% of the organic matter was water soluble with another third soluble in dichloromethane and the remainder insoluble. Within the isolated water soluble material, hydrophobic acid and hydrophilic acids plus neutrals fractions contained the largest amounts of carbon. The hydrophobic acids fraction appears to contain significant amounts of lignin type structures, spectra of the hydrophilic acids plus neutrals fraction are indicative of carbohydrates and secondary organic material. The dichloromethane soluble fraction contains a variety of organic compound families typical of many previous studies of organic aerosol speciation, including alkanes, alkanols, alkanals and alkanoic acids. Finally the water and solvent insoluble fraction exhibits a strong aromaticity as one would expect from black or elemental carbon like material; however, these spectra also show a substantial amount of aliphaticity consistent with linear side chains on the aromatic structures.

  3. Characteristics of carbonaceous aerosols emitted from peatland fire in Riau, Sumatra, Indonesia (2): Identification of organic compounds

    Science.gov (United States)

    Fujii, Yusuke; Kawamoto, Haruo; Tohno, Susumu; Oda, Masafumi; Iriana, Windy; Lestari, Puji

    2015-06-01

    Smoke emitted from Indonesian peatland fires has caused dense haze and serious air pollution in Southeast Asia such as visibility impairment and adverse health impacts. To mitigate the Indonesian peatland fire aerosol impacts, an effective strategy and international framework based on the latest scientific knowledge needs to be established. Although several attempts have been made, limited data exist regarding the chemical characteristics of peatland fire smoke for the source apportionment. In order to identify the key organic compounds of peatland fire aerosols, we conducted intensive field studies based on ground-based and source-dominated sampling of PM2.5 in Riau Province, Sumatra, Indonesia, during the peatland fire seasons in 2012. Levoglucosan was the most abundant compound among the quantified organic compounds at 8.98 ± 2.28% of the PM2.5 mass, followed by palmitic acid at 0.782 ± 0.163% and mannosan at 0.607 ± 0.0861%. Potassium ion was not appropriate for an indicator of Indonesian peatland fires due to extremely low concentrations associated with smoldering fire at low temperatures. The vanillic/syringic acids ratio was 1.06 ± 0.155 in this study and this may be a useful signature profile for peatland fire emissions. Particulate n-alkanes also have potential for markers to identify impact of Indonesian peatland fire source at a receptor site.

  4. Accommodation coefficient of HOBr on deliquescent sodium bromide aerosol particles

    Directory of Open Access Journals (Sweden)

    M. Wachsmuth

    2002-01-01

    Full Text Available Uptake of HOBr on sea salt aerosol, sea salt brine or ice is believed to be a key process providing a source of photolabile bromine (Br2 and sustaining ozone depletion cycles in the Arctic troposphere. In the present study, uptake of HOBr on sodium bromide (NaBr aerosol particles was investigated at an extremely low HOBr concentration of 300 cm-3 using the short-lived radioactive isotopes 83-86Br. Under these conditions, at maximum one HOBr molecule was taken up per particle. The rate of uptake was clearly limited by the mass accommodation coefficient, which was calculated to be 0.6 ± 0.2. This value is a factor of 10 larger than estimates used in earlier models. The atmospheric implications are discussed using the box model "MOCCA'', showing that the increase of the accommodation coefficient of HOBr by a factor of 10 only slightly affects net ozone loss, but significantly increases chlorine release.

  5. Performance of DMPS/C System in Determining Aerosol Particle Size Distribution

    International Nuclear Information System (INIS)

    An evaluation of performance of DMPS/C system TSI-3932 in determining aerosol particle size has been carried out. The evaluation consist of validity of experimentally transfer function, instrument resolution, and test of measurement accuracy and precision for monodisperse and polydisperse aerosol size distribution. Evaluation of measurement accuracy gave a deviation of 0.74 %, and evaluation of measurement precision gave variation coefficient of 0,50 % and 1.63 % for monodisperse aerosol and polydisperse aerosol respectively

  6. Algorithm of Data Reduce in Determination of Aerosol Particle Size Distribution at Damps/C

    International Nuclear Information System (INIS)

    The analysis had to do for algorithm of data reduction on Damps/C (Differential Mobility Particle Sizer with Condensation Particle Counter) system, this is for determine aerosol particle size distribution with range 0,01 μm to 1 μm in diameter. Damps/C (Differential Mobility Particle Sizer with Condensation Particle Counter) system contents are software and hardware. The hardware used determine of mobilities of aerosol particle and so the software used determine aerosol particle size distribution in diameter. The mobilities and diameter particle had connection in the electricity field. That is basic program for reduction of data and particle size conversion from particle mobility become particle diameter. The analysis to get transfer function value, Ω, is 0.5. The data reduction program to do conversation mobility basis become diameter basis with number efficiency correction, transfer function value, and poly charge particle. (author)

  7. Deliquescence and Efflorescence Processes of Aerosol Particles Studied by in situ FTIR and Raman Spectroscopy

    Institute of Scientific and Technical Information of China (English)

    Li-jun Zhao; Feng Wang; Kun Zhang; Qing-xuan Zeng; Yun-hong Zhang

    2008-01-01

    Deliquescence and efflorescence are the two most important physicochemical processes of aerosol particles.In deliquescence and efflorescence cycles of aerosol particles,many fundamental problems need to be investigated in detail on the molecular level,including ion and molecule interactions in supersaturated aerosols,metastable solid phases that may be formed,and microscopic structures and deliquescence mechanisms of aerosol particles.This paper presents a summary of the progress made in recent investigations of deliquescence and efflorescence processes of aerosol particles by four common spectral techniques,which are known as Raman/electrodynamic balance,Fourier transform infrared/aerosol flow tube,Fourier transform infrared/attenuated total reflection,and confocal Raman on a quartz substrate.

  8. Simulation of the influence of aerosol particles on Stokes parameters of polarized skylight

    International Nuclear Information System (INIS)

    Microphysical properties and chemical compositions of aerosol particles determine polarized radiance distribution in the atmosphere. In this paper, the influences of different aerosol properties (particle size, shape, real and imaginary parts of refractive index) on Stokes parameters of polarized skylight in the solar principal and almucantar planes are studied by using vector radiative transfer simulations. The results show high sensitivity of the normalized Stokes parameters due to fine particle size, shape and real part of refractive index of aerosols. It is possible to utilize the strength variations at the peak positions of the normalized Stokes parameters in the principal and almucantar planes to identify aerosol types

  9. A review of natural aerosol interactions and feedbacks within the Earth system

    OpenAIRE

    Carslaw, K. S.; Boucher, O.; Spracklen, D. V.; Mann, G.W.; J. G. L. Rae; Woodward, S.; Kulmala, M.

    2010-01-01

    The natural environment is a major source of atmospheric aerosols, including dust, secondary organic material from terrestrial biogenic emissions, carbonaceous particles from wildfires, and sulphate from marine phytoplankton dimethyl sulphide emissions. These aerosols also have a significant effect on many components of the Earth system such as the atmospheric radiative balance and photosynthetically available radiation entering the biosphere, the ...

  10. Aerosol particle properties in a South American megacity

    Science.gov (United States)

    Ulke, Ana; Torres-Brizuela, Marcela; Raga, Graciela; Baumgardner, Darrel; Cancelada, Marcela

    2015-04-01

    The subtropical city of Buenos Aires is located on the western shore of Río de la Plata, on the southeastern coast of Argentina. It is the second largest metropolitan area in South America, with a population density of around 14 thousand people per km2. When all 24 counties of the Great Buenos Aires Metropolitan Area are included it is the third-largest conurbation in Latin America, with a population of around fifteen million inhabitants. The generalized worldwide trend to concentrate human activities in urban regions that continue to expand in area, threatens the local and regional environment. Air pollution in the Buenos Aires airshed is due to local sources (mainly the mobile sources, followed by the electric power plants and some industries) and to distant sources (like biomass burning, dust, marine aerosols and occasionally volcanic ash) whose products arrive in the city area due to the regional transport patterns. Previous research suggests that ambient aerosol particle concentrations should be considered an air quality problem. A field campaign was conducted in Buenos Aires in 2011 in order to characterize some aerosol particles properties measured for the first time in the city. Measurements began in mid- April and continued until December. The field observations were done in a collaborative effort between the Universities of Mexico (UNAM) and Buenos Aires (UBA). A suite of instruments was installed on the roof of an UBA laboratory and classroom buildings (34.54° S, 58.44° W) at an altitude of approximately 30 m above sea level. The measurements included the number concentration of condensation nuclei (CN) larger than approximately 50 nm, the mass concentration of particle-bound polycyclic aromatic hydrocarbons (PPAH), the scattering (Bscat) and absorption (Babs) coefficients at 550 nm and the vertical profiles of backscattered light from aerosols at a wavelength of 910 nm using a ceilometer. In addition, a weather station recorded the meteorological

  11. Review: engineering particles using the aerosol-through-plasma method

    Energy Technology Data Exchange (ETDEWEB)

    Phillips, Jonathan [Los Alamos National Laboratory; Luhrs, Claudia C [UNM; Richard, Monique [TEMA

    2009-01-01

    For decades, plasma processing of materials on the nanoscale has been an underlying enabling technology for many 'planar' technologies, particularly virtually every aspect of modern electronics from integrated-circuit fabrication with nanoscale elements to the newest generation of photovoltaics. However, it is only recent developments that suggest that plasma processing can be used to make 'particulate' structures of value in fields, including catalysis, drug delivery, imaging, higher energy density batteries, and other forms of energy storage. In this paper, the development of the science and technology of one class of plasma production of particulates, namely, aerosol-through-plasma (A-T-P), is reviewed. Various plasma systems, particularly RF and microwave, have been used to create nanoparticles of metals and ceramics, as well as supported metal catalysts. Gradually, the complexity of the nanoparticles, and concomitantly their potential value, has increased. First, unique two-layer particles were generated. These were postprocessed to create unique three-layer nanoscale particles. Also, the technique has been successfully employed to make other high-value materials, including carbon nanotubes, unsupported graphene, and spherical boron nitride. Some interesting plasma science has also emerged from efforts to characterize and map aerosol-containing plasmas. For example, it is clear that even a very low concentration of particles dramatically changes plasma characteristics. Some have also argued that the local-thermodynamic-equilibrium approach is inappropriate to these systems. Instead, it has been suggested that charged- and neutral-species models must be independently developed and allowed to 'interact' only in generation terms.

  12. Number concentrations of solid particles from the spinning top aerosol generator

    International Nuclear Information System (INIS)

    A spinning top aerosol generator has been used to generate monodisperse methylene blue particles in the size range from 0.6 to 6 μm. The number concentrations of these aerosols have been determined by means of an optical particle counter and compared with the equivalent measurements obtained by filter collection and microscopy. (author)

  13. New aerosol particles formation in the Sao Paulo Metropolitan Area

    Science.gov (United States)

    Vela, Angel; Andrade, Maria de Fatima; Ynoue, Rita

    2016-04-01

    The Sao Paulo Metropolitan Area (SPMA), in the southeast region of Brazil, is considered a megalopolis comprised of Sao Paulo city and more 38 municipalities. The air pollutant emissions in the SPMA are related to the burning of the fuels: etanol, gasohol (gasoline with 25% ethanol) and diesel. According to CETESB (2013), the road vehicles contributed up to about 97, 87, and 80% of CO, VOCs and NOx emissions in 2012, respectively, being most of NOx associated to diesel combustion and most of CO and VOCs from gasohol and ethanol combustion. Studies conducted on ambient air pollution in the SPMA have shown that black carbon (BC) explains 21% of mass concentration of PM2.5 compared with 40% of organic carbon (OC), 20% of sulfates, and 12% of soil dust (Andrade et al., 2012). Most of the observed ambient PM2.5 mass concentration usually originates from precursors gases such as sulphur dioxide (SO2), ammonia (NH3), nitrogen oxides (NOx) and VOCs as well as through the physico-chemical processes such as the oxidation of low volatile hydrocarbons transferring to the condensed phase (McMurry et al., 2004). The Weather Research and Forecasting with Chemistry model (WRF-Chem; Grell et al. 2005), configured with three nested grid cells: 75, 15, and 3 km, is used as photochemical modeling to describe the physico-chemical processes leading to evolution of particles number and mass size distribution from a vehicular emission model developed by the IAG-USP laboratory of Atmospheric Processes and based on statistical information of vehicular activity. The spatial and temporal distributions of emissions in the finest grid cell are based on road density products compiled by the OpenStreetMap project and measurements performed inside tunnels in the SPMA, respectively. WRF-Chem simulation with coupled primary aerosol (dust and sea-salt) and biogenic emission modules and aerosol radiative effects turned on is conducted as the baseline simulation (Case_0) to evaluate the model

  14. Limits of DPUI application associated with the number of particles within actinide aerosols

    International Nuclear Information System (INIS)

    Dose per unit intake (DPUI) of radionuclides is obtained using International Commission on Radiological Protection (ICRP) models. After inhalation exposure, the first model calculates the fraction of activity deposited within the different regions of the respiratory tract, assuming that the aerosol contains an infinite number of particles. Using default parameters for workers, an exposure to one annual limit of intake (ALI) corresponds to an aerosol of 239PuO2 containing ∼1 x 106 particles. To reach such an exposure, very low particle number might be involved especially for compounds having a high specific activity. This study provides examples of exposures to actinide aerosols for which the number of particles is too low for a standard application of the ICRP model. These examples, which involve physical studies of aerosols collected at the workplace and interpretation of bioassay data, show that the number of particles of the aerosol can be the main limit for the application of DPUI after inhalation exposure. (authors)

  15. Single-particle Analyses of Compositions, Morphology, and Viscosity of Aerosol Particles Collected During GoAmazon2014

    Science.gov (United States)

    Adachi, K.; Gong, Z.; Bateman, A. P.; Martin, S. T.; Cirino, G. G.; Artaxo, P.; Sedlacek, A. J., III; Buseck, P. R.

    2014-12-01

    Single-particle analysis using transmission electron microscopy (TEM) shows composition and morphology of individual aerosol particles collected during the GoAmazon2014 campaign. These TEM results indicate aerosol types and mixing states, both of which are important for evaluating particle optical properties and cloud condensation nuclei activity. The samples were collected at the T3 site, which is located in the Amazon forest with influences from the urban pollution plume from Manaus. Samples were also collected from the T0 site, which is in the middle of the jungle with minimal to no influences of anthropogenic sources. The aerosol particles mainly originated from 1) anthropogenic pollution (e.g., nanosphere soot, sulfate), 2) biogenic emissions (e.g., primary biogenic particles, organic aerosols), and 3) long-range transport (e.g., sea salts). We found that the biogenic organic aerosol particles contain homogeneously distributed potassium. Particle viscosity is important for evaluating gas-particle interactions and atmospheric chemistry for the particles. Viscosity can be estimated from the rebounding behavior at controlled relative humidities, i.e., highly viscous particles display less rebound on a plate than low-viscosity particles. We collected 1) aerosol particles from a plate (non-rebounded), 2) those that had rebounded from the plate and were then captured onto an adjacent sampling plate, and 3) particles from ambient air using a separate impactor sampler. Preliminary results show that more than 90% of non-rebounded particles consisted of nanosphere soot with or without coatings. The coatings mostly consisted of organic matter. Although rebounded particles also contain nanosphere soot (number fraction 64-69%), they were mostly internally mixed with sulfate, organic matter, or their mixtures. TEM tilted images suggested that the rebounded particles were less deformed on the substrate, whereas the non-rebounded particles were more deformed, which could

  16. Online coupling of pure O2 thermo-optical methods - 14C AMS for source apportionment of carbonaceous aerosols

    Science.gov (United States)

    Agrios, Konstantinos; Salazar, Gary; Zhang, Yan-Lin; Uglietti, Chiara; Battaglia, Michael; Luginbühl, Marc; Ciobanu, Viorela Gabriela; Vonwiller, Matthias; Szidat, Sönke

    2015-10-01

    This paper reports on novel separation methods developed for the direct determination of 14C in organic carbon (OC) and elemental carbon (EC), two sub-fractions of total carbon (TC) of atmospheric air particulate matter. Until recently, separation of OC and EC has been performed off-line by manual and time-consuming techniques that relied on the collection of massive CO2 fractions. We present here two on-line hyphenated techniques between a Sunset OC/EC analyzer and a MICADAS (MIni radioCArbon DAting System) accelerator mass spectrometer (AMS) equipped with a gas ion source. The first implementation facilitates the direct measurement in the low sample size range (<10 μg C) with high throughput on a routine basis, while the second explores the potential for a continuous-flow real-time CO2 gas feed into the ion source. The performance achieved with reference materials and real atmospheric samples will be discussed to draw conclusions on the improvement offered in the field of 14C aerosol source apportionment.

  17. Real-time measurement of aerosol particle concentration at high temperatures; Hiukkaspitoisuuden reaaliaikainen mittaaminen korkeassa laempoetilassa

    Energy Technology Data Exchange (ETDEWEB)

    Keskinen, J.; Hautanen, J.; Laitinen, A. [Tampere Univ. of Technology (Finland). Physics

    1997-10-01

    The aim of this project is to develop a new method for continuous aerosol particle concentration measurement at elevated temperatures (up to 800-1000 deg C). The measured property of the aerosol particles is the so called Fuchs surface area. This quantity is relevant for diffusion limited mass transfer to particles. The principle of the method is as follows. First, aerosol particles are charged electrically by diffusion charging process. The charging takes place at high temperature. After the charging, aerosol is diluted and cooled. Finally, aerosol particles are collected and the total charge carried by the aerosol particles is measured. Particle collection and charge measurement take place at low temperature. Benefits of this measurement method are: particles are charged in-situ, charge of the particles is not affected by the temperature and pressure changes after sampling, particle collection and charge measurement are carried out outside the process conditions, and the measured quantity is well defined. The results of this study can be used when the formation of the fly ash particles is studied. Another field of applications is the study and the development of gasification processes. Possibly, the method can also be used for the monitoring the operation of the high temperature particle collection devices. (orig.)

  18. A combined particle trap/HTDMA hygroscopicity study of mixed inorganic/organic aerosol particles

    Directory of Open Access Journals (Sweden)

    A. A. Zardini

    2008-03-01

    Full Text Available Atmospheric aerosols are often mixtures of inorganic and organic material. Organics can represent a large fraction of the total aerosol mass and are comprised of water-soluble and insoluble compounds. Increasing attention was paid in the last decade to the capability of mixed inorganic/organic aerosol particles to take up water (hygroscopicity. We performed hygroscopicity measurements of internally mixed particles containing ammonium sulfate and carboxylic acids (citric, glutaric, adipic acid in parallel with an electrodynamic balance (EDB and a hygroscopicity tandem differential mobility analyzer (HTDMA. The organic compounds were chosen to represent three distinct physical states. During hygroscopicity cycles covering hydration and dehydration measured by the EDB and the HTDMA, pure citric acid remained always liquid, adipic acid remained always solid, while glutaric acid could be either. We show that the hygroscopicity of mixtures of the above compounds is well described by the Zdanovskii-Stokes-Robinson (ZSR relationship as long as the two-component particle is completely liquid in the ammonium sulfate/citric acid and in the ammonium sulfate/glutaric acid cases. However, we observe significant discrepancies compared to what is expected from bulk thermodynamics when a solid component is present. We explain this in terms of a complex morphology resulting from the crystallization process leading to veins, pores, and grain boundaries which allow for water sorption in excess of bulk thermodynamic predictions caused by the inverse Kelvin effect on concave surfaces.

  19. Dual isotope (13C-14C) Studies of Water-Soluble Organic Carbon (WSOC) Aerosols in South and East Asia

    OpenAIRE

    Kirillova, Elena N.

    2013-01-01

    Atmospheric aerosols may be emitted directly as particles (primary) or formed from gaseous precursors (secondary) from different natural and anthropogenic sources. The highly populated South and East Asia regions are currently in a phase of rapid economic growth to which high emissions of carbonaceous aerosols are coupled. This leads to generally poor air quality and a substantial impact of anthropogenic aerosols on the regional climate. However, the emissions of different carbon aerosol comp...

  20. Composition and hygroscopicity of aerosol particles at Mt. Lu in South China: Implications for acid precipitation

    Science.gov (United States)

    Li, Weijun; Chi, Jianwei; Shi, Zongbo; Wang, Xinfeng; Chen, Bin; Wang, Yan; Li, Tao; Chen, Jianmin; Zhang, Daizhou; Wang, Zifa; Shi, Chune; Liu, Liangke; Wang, Wenxing

    2014-09-01

    Physicochemical properties of aerosol particles were studied at Mt. Lu, an elevated site (115°59‧E, 29°35‧N, 1165 m) within the acid precipitation area. Northeast winds transport copious amounts of air pollutants and water vapor from the Yangtze River Delta into this acid precipitation area. NH4+ and SO42- are the dominant ions in PM2.5 and determine aerosol acidity. Individual particle analysis shows abundant S-rich and metals (i.e. Fe-, Zn-, Mn-, and Pb-rich) particles. Unlike aerosol particles in North China and urban areas, there are little soot and mineral particles at Mt. Lu. Lack of mineral particles contributed to the higher acidity in precipitation in the research area. Nano-sized spherical metal particles were observed to be embedded in 37% of S-rich particles. These metal particles were likely originated from heavy industries and fired-power plants. Hygroscopic experiments show that most particles start to deliquesce at 73-76% but organic coating lowers the particle deliquescence relative humidity (DRH) to 63-73%. The DRHs of these aerosol particles are clearly smaller than that of pure ammonium sulfate particles which is 80%. Since RH in ambient air was relatively high, ranging from 65% to 85% during our study period, most particles at our sampling site were in liquid phase. Our results suggest that liquid phase reactions in aerosol particles may contribute to SO2 to sulfuric acid conversion in the acid precipitation area.

  1. Concentrations and light absorption characteristics of carbonaceous aerosol in PM2.5 and PM10 of Lhasa city, the Tibetan Plateau

    Science.gov (United States)

    Li, Chaoliu; Chen, Pengfei; Kang, Shichang; Yan, Fangping; Hu, Zhaofu; Qu, Bin; Sillanpää, Mika

    2016-02-01

    Light absorption properties of carbonaceous aerosol strongly influence the Earth's radiative balance, yet the related knowledge is limited for the Tibetan Plateau (TP), the highest and largest plateau in the world. In this study, organic carbon (OC), elemental carbon (EC) and water soluble organic carbon (WSOC) of PM2.5 and PM10 of Lhasa collected from May 2013 to March 2014 were studied. It showed that daily-average concentrations of OC, EC and WSOC of PM2.5 and PM10 were lower than those of other megacities. Lhasa PM2.5 was characterized by low OC/EC ratio (1.46 ± 0.55), which was similar to that of Lhasa roadside PM2.5 (1.25 ± 0.45), reflecting mainly direct influence of primary emissions and less secondary formation. Hence, although Lhasa atmosphere is relatively clean, it is intensively influenced by local vehicle emissions. Mass absorption cross-section of EC (MACEC) for both PM2.5 and PM10 at 632 nm were 7.19 ± 1.19 m2 g-1 and 7.98 ± 2.32 m2 g-1, respectively, both of which had similar variation patterns to OC/EC and secondary OC (SOC)/OC, indicating that the increase of MACEC might be caused by coating with organic aerosol. Additionally, the loading of EC for both PM2.5 and PM10 showed logarithmic relationships with those of optical attenuation (ATN) of EC, implying that the shadowing effect enhanced logarithmic with increased EC concentration. MAC of WSOC at 365 nm for PM2.5 (0.74 ± 0.22 m2 g-1) and PM10 (0.78 ± 0.21 m2 g-1) were also close to reported values of other cities mainly influenced by fossil combustion. Additionally, attenuation at 365 nm of WSOC of both PM2.5 and PM10 showed the same relationship with their WSOC concentrations, implying no difference for light absorption properties of WSOC for these two grain sizes.

  2. Formation of highly porous aerosol particles by atmospheric freeze-drying in ice clouds.

    Science.gov (United States)

    Adler, Gabriela; Koop, Thomas; Haspel, Carynelisa; Taraniuk, Ilya; Moise, Tamar; Koren, Ilan; Heiblum, Reuven H; Rudich, Yinon

    2013-12-17

    The cycling of atmospheric aerosols through clouds can change their chemical and physical properties and thus modify how aerosols affect cloud microphysics and, subsequently, precipitation and climate. Current knowledge about aerosol processing by clouds is rather limited to chemical reactions within water droplets in warm low-altitude clouds. However, in cold high-altitude cirrus clouds and anvils of high convective clouds in the tropics and midlatitudes, humidified aerosols freeze to form ice, which upon exposure to subsaturation conditions with respect to ice can sublimate, leaving behind residual modified aerosols. This freeze-drying process can occur in various types of clouds. Here we simulate an atmospheric freeze-drying cycle of aerosols in laboratory experiments using proxies for atmospheric aerosols. We find that aerosols that contain organic material that undergo such a process can form highly porous aerosol particles with a larger diameter and a lower density than the initial homogeneous aerosol. We attribute this morphology change to phase separation upon freezing followed by a glass transition of the organic material that can preserve a porous structure after ice sublimation. A porous structure may explain the previously observed enhancement in ice nucleation efficiency of glassy organic particles. We find that highly porous aerosol particles scatter solar light less efficiently than nonporous aerosol particles. Using a combination of satellite and radiosonde data, we show that highly porous aerosol formation can readily occur in highly convective clouds, which are widespread in the tropics and midlatitudes. These observations may have implications for subsequent cloud formation cycles and aerosol albedo near cloud edges. PMID:24297908

  3. Ensemble projections of wildfire activity and carbonaceous aerosol concentrations over the western United States in the mid-21st century

    Science.gov (United States)

    Yue, Xu; Mickley, Loretta J.; Logan, Jennifer A.; Kaplan, Jed O.

    2013-10-01

    We estimate future wildfire activity over the western United States during the mid-21st century (2046-2065), based on results from 15 climate models following the A1B scenario. We develop fire prediction models by regressing meteorological variables from the current and previous years together with fire indexes onto observed regional area burned. The regressions explain 0.25-0.60 of the variance in observed annual area burned during 1980-2004, depending on the ecoregion. We also parameterize daily area burned with temperature, precipitation, and relative humidity. This approach explains ˜0.5 of the variance in observed area burned over forest ecoregions but shows no predictive capability in the semi-arid regions of Nevada and California. By applying the meteorological fields from 15 climate models to our fire prediction models, we quantify the robustness of our wildfire projections at midcentury. We calculate increases of 24-124% in area burned using regressions and 63-169% with the parameterization. Our projections are most robust in the southwestern desert, where all GCMs predict significant (p ecoregions, more GCMs predict significant increases in future area burned with the parameterization than with the regressions, because the latter approach is sensitive to hydrological variables that show large inter-model variability in the climate projections. The parameterization predicts that the fire season lengthens by 23 days in the warmer and drier climate at midcentury. Using a chemical transport model, we find that wildfire emissions will increase summertime surface organic carbon aerosol over the western United States by 46-70% and black carbon by 20-27% at midcentury, relative to the present day. The pollution is most enhanced during extreme episodes: above the 84th percentile of concentrations, OC increases by ˜90% and BC by ˜50%, while visibility decreases from 130 km to 100 km in 32 Federal Class 1 areas in Rocky Mountains Forest.

  4. Sources of carbonaceous aerosols and deposited black carbon in the Arctic in winter-spring: implications for radiative forcing

    Directory of Open Access Journals (Sweden)

    Q. Wang

    2011-12-01

    Full Text Available We use a global chemical transport model (GEOS-Chem CTM to interpret observations of black carbon (BC and organic aerosol (OA from the NASA ARCTAS aircraft campaign over the North American Arctic in April 2008, as well as longer-term records in surface air and in snow (2007–2009. BC emission inventories for North America, Europe, and Asia in the model are tested by comparison with surface air observations over these source regions. Russian open fires were the dominant source of OA in the Arctic troposphere during ARCTAS but we find that BC was of prevailingly anthropogenic (fossil fuel and biofuel origin, particularly in surface air. This source attribution is confirmed by correlation of BC and OA with acetonitrile and sulfate in the model and in the observations. Asian emissions are the main anthropogenic source of BC in the free troposphere but European, Russian and North American sources are also important in surface air. Russian anthropogenic emissions appear to dominate the source of BC in Arctic surface air in winter. Model simulations for 2007–2009 (to account for interannual variability of fires show much higher BC snow content in the Eurasian than the North American Arctic, consistent with the limited observations. We find that anthropogenic sources contribute 90% of BC deposited to Arctic snow in January-March and 60% in April–May 2007–2009. The mean decrease in Arctic snow albedo from BC deposition is estimated to be 0.6% in spring, resulting in a regional surface radiative forcing consistent with previous estimates.

  5. Sources of carbonaceous aerosols and deposited black carbon in the Arctic in winter–spring: implications for radiative forcing

    Directory of Open Access Journals (Sweden)

    Q. Wang

    2011-07-01

    Full Text Available We use a global chemical transport model (GEOS-Chem CTM to interpret observations of black carbon (BC and organic aerosol (OA from the NASA ARCTAS aircraft campaign over the North American Arctic in April 2008, together with longer-term records in surface air and in snow. We find that Russian open fires were the dominant source of OA in the troposphere during ARCTAS but that BC was more of anthropogenic origin, particularly in surface air. This source attribution is confirmed by correlation of BC and OA with acetonitrile and sulfate in the model and in the observations. Asian emissions are the main anthropogenic source of BC in the free troposphere but European, Russian and North American sources are also important in surface air. Russian anthropogenic emissions appear to dominate the Arctic source of BC in surface air in winter. Open fire influences on Arctic surface BC in spring are much higher in the Eurasian than in the North American sector. Most of the BC transported to the Arctic in the lower troposphere is deposited within the Arctic, in contrast to the BC transported at higher altitudes. Pan-Arctic 2007–2009 observations of BC concentrations in snow are well reproduced by the model, with maximum values in the Russian Arctic and much lower values in the North American Arctic. We find that anthropogenic sources contribute 90% of BC deposited to Arctic snow in January–March and 57% in April–May 2007–2009. The mean decrease in Arctic snow albedo from BC deposition is estimated to be 0.6% in spring 2007–2009, resulting in a regional surface radiative forcing consistent with previous estimates.

  6. Identification of origin of single aerosol particles using polycapillary X-ray lens

    International Nuclear Information System (INIS)

    A micro X-ray fluorescence (Micro-XRF) spectrometer based on a polycapillary focusing X-ray lens (PFXRL) and a laboratory X-ray source was designed to carry out the XRF analysis of single aerosol particles. The minimum detection limit (MDL) of this Micro-XRF spectrometer was 9 ppm for the Fe-Kα. The percentage of the particles of vehicle exhaust among aerosol particles was studied in Beijing, Chinese capital, during the test of odd-even driving restrictions for Beijing 2008 Olympics Games. This Micro-XRF spectrometer had potential applications in the analysis of single aerosol particles.

  7. Hygroscopic properties of aerosol particles at high relative humidity and their diurnal variations in the North China Plain

    Directory of Open Access Journals (Sweden)

    P. F. Liu

    2011-01-01

    box model (PartMC-MOSAIC suggest that the diurnal variations of aerosol hygroscopicity and mixing state were mainly caused by the evolution of the atmospheric mixing layer. The shallow nocturnal boundary layer during the night facilitated the accumulation of freshly emitted carbonaceous particles (mainly hydrophobic near the surface while in the morning turbulence entrained the more aged and more hygroscopic particles from aloft and diluted the NH particles near the surface resulting in a decrease in the fraction of NH particles.

  8. Classification of monodisperse aerosol particles using an adjustable soft X-ray charger

    OpenAIRE

    Han, Bangwoo; Shimada, Manabu; Okuyama, Kikuo; Choi, Mansoo

    2003-01-01

    At high concentrations of ambient bipolar ions, charged aerosol particles show a stationary charging state as a function of particle size. When the particle diameter exceeds 0.1 μm, a considerable fraction of multiply charged particles is present, which hinders size classification of particles, when a differential mobility analyzer (DMA) is used. However, at low ion concentrations, particle charging by the ions can be suppressed, and in principle, the production of multiply charged particles ...

  9. Real-time detection method and system for identifying individual aerosol particles

    Science.gov (United States)

    Gard, Eric E.; Coffee, Keith R.; Frank, Matthias; Tobias, Herbert J.; Fergenson, David P.; Madden, Norm; Riot, Vincent J.; Steele, Paul T.; Woods, Bruce W.

    2007-08-21

    An improved method and system of identifying individual aerosol particles in real time. Sample aerosol particles are collimated, tracked, and screened to determine which ones qualify for mass spectrometric analysis based on predetermined qualification or selection criteria. Screening techniques include one or more of determining particle size, shape, symmetry, and fluorescence. Only qualifying particles passing all screening criteria are subject to desorption/ionization and single particle mass spectrometry to produce corresponding test spectra, which is used to determine the identities of each of the qualifying aerosol particles by comparing the test spectra against predetermined spectra for known particle types. In this manner, activation cycling of a particle ablation laser of a single particle mass spectrometer is reduced.

  10. Volatility of Nuclei Mode Arctic Aerosol Particles during Summer

    Czech Academy of Sciences Publication Activity Database

    Biskos, J.G.; Vratolis, S.; Ondráček, Jakub; Karanasioy, A.A.; Eleftheriadis, K.

    -: -, 2009, T160A13. [European Aerosol Conference 2009. Karlsruhe (DE), 06.09.2009-11.09.2009] Institutional research plan: CEZ:AV0Z40720504 Keywords : arctic aerosol * nucleation mode * volatility Subject RIV: CF - Physical ; Theoretical Chemistry

  11. METHODS OF CALCULATINAG LUNG DELIVERY AND DEPOSITION OF AEROSOL PARTICLES

    Science.gov (United States)

    Lung deposition of aerosol is measured by a variety of methods. Total lung deposition can be measured by monitoring inhaled and exhaled aerosols in situ by laser photometry or by collecting the aerosols on filters. The measurements can be performed accurately for stable monod...

  12. Effects of aerosol particle size on dispersion and continuous air monitor response in a plutonium laboratory

    International Nuclear Information System (INIS)

    The effectiveness of continuous air monitors (CAMs) in protecting plutonium workers depends on the efficiency of aerosol transport from the release point to the CAM. The main processes for aerosol transport are diffusion, forced convection, and gravitational settling. The transport of particles relative to each of these processes depends on particle size. Studies have shown that activity median aerodynamic diameters for plutonium aerosols can range from less than 0.1 μm to greater than 10 μm. The purpose of this study was to characterize the influence of particle size on aerosol transport and CAM response in a plutonium laboratory. Polydisperse dioctyl sebacate oil aerosols were released from multiple locations within a plutonium laboratory at Los Alamos National Laboratory. An array of Laser Particle counters (LPCs) positioned in the laboratory measured time resolved aerosol dispersion. Aerosol concentrations were binned into two size ranges: (1) 0.5 μm to 5.0 μm, and (2) those greater than 5.0 μm. Statistical comparisons were done and the results suggested that transport efficiency was greater for smaller particles than larger particles in this laboratory. This result suggested the importance of using particles of similar physical characteristics to those of the source when doing tests to decide optimal placement of CAMs

  13. The Formation of Porous Membranes by Filtration of Aerosol Nano-particles

    DEFF Research Database (Denmark)

    Andersen, Sune Klint; Johannessen, Tue; Mosleh, Majid;

    2002-01-01

    Flame-generated aerosol particles of Al2O3 were deposited by gas filtration on two types of porous and ceramic tubes of α-Al2O3 with mean pore diameters of 450 and 2700 nm, respectively. The particles were aggregates with average mobility diameters in the range of 30¨¢100 nm and primary particle...... membrane layer. This effect is particularly significant for the aerosol particles with the lowest mean size, probably due to particles deposited in the pore mouths of the substrate. The particles and the deposited membranes are X-ray amorphous but retain their specific surface area on heating to even high...

  14. Characterization of individual submicrometer aerosol particles collected in Incheon, Korea, by quantitative transmission electron microscopy energy-dispersive X-ray spectrometry

    Science.gov (United States)

    Geng, Hong; Kang, Sujin; Jung, Hae-Jin; ChoëL, Marie; Kim, Hyekyeong; Ro, Chul-Un

    2010-08-01

    For the last decade the Monte Carlo calculation method has been proven to be an excellent tool for accurately simulating electron-solid interactions in atmospheric individual particles of micrometer size. Although it was designed for application to scanning electron microscopy, in the present study it is demonstrated that the Monte Carlo calculation can also be applied in a quantitative single particle analysis using transmission electron microscopy (TEM) with an ultrathin window energy-dispersive X-ray (EDX) spectrometer with a high accelerating voltage (200 kV). By utilizing an iterative reverse Monte Carlo simulation combined with successive approximation, atomic elemental concentrations (including low-Z elements) of submicrometer standard particles were determined with high accuracy for electron beam refractory particles such as NaCl, KCl, SiO2, Fe2O3, Na2SO4, K2SO4, CaCO3, and CaSO4. On the basis of quantitative X-ray analysis together with morphological information from TEM images, overall 1638 submicrometer individual particles from 10 sets of aerosol samples collected in Incheon, Korea, were identified. The most frequently encountered particle types are carbonaceous and (NH4)2SO4/NH4HSO4-containing particles, followed by mineral (e.g., aluminosilicate, SiO2, CaCO3), sea salt, K-rich (e.g., K2SO4 and KCl), Fe-rich, fly ash, and transition or heavy-metal-containing (e.g., ZnSO4, ZnCl2, PbSO4) particles. The relative abundances of the submicrometer particle types vary among samples collected in different seasons and also depend on different air mass transport routes. This study demonstrates that the quantitative TEM-EDX individual particle analysis is a useful and reliable technique in characterizing urban submicrometer aerosol particles.

  15. Comparison between CARIBIC Aerosol Samples Analysed by Accelerator-Based Methods and Optical Particle Counter Measurements

    OpenAIRE

    B. G. Martinsson; J. Friberg; Andersson, S M; Weigelt, A; Hermann, M.; D. Assmann; J. Voigtländer; C. A. M. Brenninkmeijer; Velthoven, P. J. F.; Zahn, A.

    2014-01-01

    Inter-comparison of results from two kinds of aerosol systems in the CARIBIC (Civil Aircraft for the Regular Investigation of the atmosphere Based on a Instrument Container) passenger aircraft based observatory, operating during intercontinental flights at 9–12 km altitude, is presented. Aerosol from the lowermost stratosphere (LMS), the extra-tropical upper troposphere (UT) and the tropical mid troposphere (MT) were investigated. Aerosol particle volume concentration measur...

  16. An aerosol dynamics model for simulating particle formation and growth in a mixed flow chamber

    OpenAIRE

    Vesterinen, M.; Korhonen, H.; Joutsensaari, J.; P. Yli-Pirilä; Laaksonen, A.; Lehtinen, K. E. J.

    2011-01-01

    In this work we model the aerosol size distribution dynamics in a mixed flow chamber in which new particles are formed via nucleation and subsequent condensation of oxidation products of VOCs emitted from Norway spruce seedlings. The microphysical processes included in the model are nucleation, condensation, deposition and coagulation. The aerosol dynamics in the chamber is a competition between aerosol growth and scavenging/deposition whi...

  17. Airborne measurements of trace gas and aerosol particle emissions from biomass burning in Amazonia

    OpenAIRE

    Guyon, P; Frank, G. P.; M. Welling; D. Chand; Artaxo, P.; L. Rizzo; Nishioka, G.; Kolle, O.; Fritsch, H.; Silva Dias, M. A. F.; L. V. Gatti; Cordova, A. M.; Andreae, M.O.

    2005-01-01

    As part of the LBA-SMOCC (Large-Scale Biosphere-Atmosphere Experiment in Amazonia – Smoke, Aerosols, Clouds, Rainfall, and Climate) 2002 campaign, we studied the emission of carbon monoxide (CO), carbon dioxide (CO2), and aerosol particles from Amazonian deforestation fires using an instrumented aircraft. Emission ratios for aerosol number (CN) relative to CO (ERCN/CO) fell in the range 14–32 cm-3&nbs...

  18. Method and device for detecting and identifying bio-aerosol particles in the air

    OpenAIRE

    Stowers. M.A.; van Wuijckhuijse, A.L.; Marijnissen, J.C.; Kientz, C.E.

    2002-01-01

    In a method for detecting and identifying bioaerosol particles in the air, the bioaerosol particles in a particle stream are selected in an ATOFMS (aerosol time-of-flight mass spectrometer) by means of fluorescence techniques, and only the selected bioaerosol particles are ionized, for instance on the basis of MALDI (matrix-assisted laser desorption/ionization), after which the resulting ions are detected and the bioaerosol particles are identified.; The selection of bioaerosol particles take...

  19. Electron mean free path from angle-dependent photoelectron spectroscopy of aerosol particles

    CERN Document Server

    Goldmann, Maximilian; West, Adam H C; Yoder, Bruce L; Signorell, Ruth

    2015-01-01

    We propose angle-resolved photoelectron spectroscopy of aerosol particles as an alternative way to determine the electron mean free path of low energy electrons in solid and liquid materials. The mean free path is obtained from fits of simulated photoemission images to experimental ones over a broad range of different aerosol particle sizes. The principal advantage of the aerosol approach is twofold. Firstly, aerosol photoemission studies can be performed for many different materials, including liquids. Secondly, the size-dependent anisotropy of the photoelectrons can be exploited in addition to size-dependent changes in their kinetic energy. These finite size effects depend in different ways on the mean free path and thus provide more information on the mean free path than corresponding liquid jet, thin film, or bulk data. The present contribution is a proof of principle employing a simple model for the photoemission of electrons and preliminary experimental data for potassium chloride aerosol particles.

  20. Electron mean free path from angle-dependent photoelectron spectroscopy of aerosol particles

    International Nuclear Information System (INIS)

    We propose angle-resolved photoelectron spectroscopy of aerosol particles as an alternative way to determine the electron mean free path of low energy electrons in solid and liquid materials. The mean free path is obtained from fits of simulated photoemission images to experimental ones over a broad range of different aerosol particle sizes. The principal advantage of the aerosol approach is twofold. First, aerosol photoemission studies can be performed for many different materials, including liquids. Second, the size-dependent anisotropy of the photoelectrons can be exploited in addition to size-dependent changes in their kinetic energy. These finite size effects depend in different ways on the mean free path and thus provide more information on the mean free path than corresponding liquid jet, thin film, or bulk data. The present contribution is a proof of principle employing a simple model for the photoemission of electrons and preliminary experimental data for potassium chloride aerosol particles

  1. Reproducing the optical properties of fine desert dust aerosols using ensembles of simple model particles

    International Nuclear Information System (INIS)

    Single scattering optical properties are calculated for a proxy of fine dust aerosols at a wavelength of 0.55 μm. Spherical and spheroidal model particles are employed to fit the aerosol optical properties and to retrieve information about the physical parameters characterising the aerosols. It is found that spherical particles are capable of reproducing the scalar optical properties and the forward peak of the phase function of the dust aerosols. The effective size parameter of the aerosol ensemble is retrieved with high accuracy by using spherical model particles. Significant improvements are achieved by using spheroidal model particles. The aerosol phase function and the other diagonal elements of the Stokes scattering matrix can be fitted with high accuracy, whereas the off-diagonal elements are poorly reproduced. More elongated prolate and more flattened oblate spheroids contribute disproportionately strongly to the optimised shape distribution of the model particles and appear to be particularly useful for achieving a good fit of the scattering matrix. However, the clear discrepancies between the shape distribution of the aerosols and the shape distribution of the spheroidal model particles suggest that the possibilities of extracting shape information from optical observations are rather limited

  2. Aerosol particle transport modeling for preclosure safety studies of nuclear waste repositories

    International Nuclear Information System (INIS)

    An important concern for preclosure safety analysis of a nuclear waste repository is the potential release to the environment of respirable aerosol particles. Such particles, less than 10 μm in aerodynamic diameter, may have significant adverse health effects if inhaled. To assess the potential health effects of these particles, it is not sufficient to determine the mass fraction of respirable aerosol. The chemical composition of the particles is also of importance since different radionuclides may pose vastly different health hazards. Thus, models are needed to determine under normal and accident conditions the particle size and the chemical composition distributions of aerosol particles as a function of time and of position in the repository. In this work a multicomponent sectional aerosol model is used to determine the aerosol particle size and composition distributions in the repository. A range of aerosol mass releases with varying mean particle sizes and chemical compositions is used to demonstrate the sensitivities and uncertainties of the model. Decontamination factors for some locations in the repository are presented. 8 refs., 1 tab

  3. LOAC: a small aerosol optical counter/sizer for ground-based and balloon measurements of the size distribution and nature of atmospheric particles – Part 1: Principle of measurements and instrument evaluation

    Directory of Open Access Journals (Sweden)

    J.-B. Renard

    2015-01-01

    Full Text Available The study of aerosols in the troposphere and in the stratosphere is of major importance both for climate and air quality studies. Among the numerous instruments available, aerosol particles counters provide the size distribution in diameter range from few hundreds of nm to few tens of μm. Most of them are very sensitive to the nature of aerosols, and this can result in significant biases in the retrieved size distribution. We describe here a new versatile optical particle/sizer counter (OPC named LOAC (Light Optical Aerosols Counter, which is light and compact enough to perform measurements not only at the surface but under all kinds of balloons in the troposphere and in the stratosphere. LOAC is an original OPC performing observations at two scattering angles. The first one is around 12°, and is almost insensitive to the nature of the particles; the second one is around 60° and is strongly sensitive to the refractive index of the particles. By combining measurement at the two angles, it is possible to retrieve accurately the size distribution and to estimate the nature of the dominant particles (droplets, carbonaceous, salts and mineral particles in several size classes. This speciation is based on calibration charts obtained in the laboratory. Several campaigns of cross-comparison of LOAC with other particle counting instruments and remote sensing photometers have been conducted to validate both the size distribution derived by LOAC and the retrieved particle number density. The speciation of the aerosols has been validated in well-defined conditions including urban pollution, desert dust episodes, fog, and cloud. Comparison with reference aerosol mass monitoring instruments also shows that the LOAC measurements can be successfully converted to mass concentrations. All these tests indicate that no bias is present in the LOAC measurements and in the corresponding data processing.

  4. Evaluation of cell sorting aerosols and containment by an optical airborne particle counter.

    Science.gov (United States)

    Xie, Mike; Waring, Michael T

    2015-08-01

    Understanding aerosols produced by cell sorting is critical to biosafety risk assessment and validation of containment efficiency. In this study an Optical Airborne Particle Counter was used to analyze aerosols produced by the BD FACSAria and to assess the effectiveness of its aerosol containment. The suitability of using this device to validate containment was directly compared to the Glo-Germ method put forth by the International Society for Advancement of Cytometry (ISAC) as a standard for testing. It was found that high concentrations of aerosols ranging from 0.3 µm to 10 µm can be detected in failure mode, with most less than 5 µm. In most cases, while numerous aerosols smaller than 5 µm were detected by the Optical Airborne Particle Counter, no Glo-Germ particles were detected, indicating that small aerosols are under-evaluated by the Glo-Germ method. The results demonstrate that the Optical Airborne Particle Counter offers a rapid, economic, and quantitative analysis of cell sorter aerosols and represents an improved method over Glo-Germ for the task of routine validation and monitoring of aerosol containment for cell sorting. PMID:26012776

  5. Nuclear microprobe analysis and source apportionment of individual atmospheric aerosol particles

    International Nuclear Information System (INIS)

    In atmospheric aerosol reserach, one key issue is to determine the sources of the airborne particles. Bulk PIXE analysis coupled with receptor modeling provides a useful, but limited view of the aerosol sources influencing one particular site or sample. The scanning nuclear microprobe (SNM) technique is a microanalytical technique that gives unique information on individual aerosol particles. In the SNM analyses a 1.0 μm size 2.4 MeV proton beam from the Oxford SNM was used. The trace elements with Z>11 were measured by the particle induced X-ray emission (PIXE) method with detection limits in the 1-10 ppm range. Carbon, nitrogen and oxygen are measured simultaneously using Rutherford backscattering spectrometry (RBS). Atmospheric aerosol particles were collected at the Brazilian Antarctic Station and at biomass burning sites in the Amazon basin tropical rain forest in Brazil. In the Antarctic samples, the sea-salt aerosol particles were clearly predominating, with NaCl and CaSO4 as major compounds with several trace elements as Al, Si, P, K, Mn, Fe, Ni, Cu, Zn, Br, Sr, and Pb. Factor analysis of the elemental data showed the presence of four components: 1) Soil dust particles; 2) NaCl particles; 3) CaSO4 with Sr; and 4) Br and Mg. Strontium, observed at 20-100 ppm levels, was always present in the CaSO4 particles. The hierarchical cluster procedure gave results similar to the ones obtained through factor analysis. For the tropical rain forest biomass burning aerosol emissions, biogenic particles with a high organic content dominate the particle population, while K, P, Ca, Mg, Zn, and Si are the dominant elements. Zinc at 10-200 ppm is present in biogenic particles rich in P and K. The quantitative aspects and excellent detection limits make SNM analysis of individual aerosol particles a very powerful analytical tool. (orig.)

  6. Identification of source contributions to visibility-reducing organic aerosols in the vicinity of Grand Canyon National Park. Interim final report

    Energy Technology Data Exchange (ETDEWEB)

    Mazurek, M.A.; Hallock, K.A.; Leach, M. [Brookhaven National Lab., Upton, NY (United States); Mason-Jones, M.; Mason-Jones, H.; Salmon, L.G.; Winner, D.A.; Cass, G.R. [California Inst. of Tech., Pasadena, CA (United States). Dept. of Environmental Engineering Science

    1993-06-01

    Sulfates and carbonaceous aerosols are the largest contributors to the fine particle burden in the atmosphere near Grand Canyon National Park. While the effects of sulfate particles on visibility at the Grand Canyon has been extensively studied, much less is known about the nature and origin of the carbonaceous aerosols that are present. This disparity in understanding arises from at least two causes: aerosol carbon data for the region are less plentiful and many of the sources that could contribute to that organic aerosol are both diverse and not well characterized. The objective of this present study is to examine the origin of the carbonaceous aerosol at Grand Canyon National Park during the summer season based on molecular tracer techniques applied to source and ambient samples collected specifically for this purpose.

  7. Ion-UHMA: a model for simulating the dynamics of neutral and charged aerosol particles.

    Energy Technology Data Exchange (ETDEWEB)

    Leppae, J.; Kerminen, V.-M. (Finnish Meteorological Institute, Climate Change Research, Helsinki (Finland)); Gagne, S.; Manninen, H. E.; Nieminen, T.; Kulmala, M. (Dept. of Physics, Univ. of Helsinki (Finland)); Laakso, L. (Dept. of Physics, Univ. of Helsinki (Finland); School of Physical and Chemical Sciences, North-West Univ. Potchefstroom (South Africa)); Korhonen, H. (Univ. of Kuopio, Dept. of Physics (Finland)); Lehtinen, K. E. J. (Univ. of Kuopio, Dept. of Physics (Finland); Finnish Meteorological Institute, Kuopio Unit (Finland))

    2009-07-01

    A new aerosol dynamical box model, Ion-UHMA (University of Helsinki Multicomponent Aerosol model for neutral and charged particles), is introduced in this paper. The model includes basic dynamical processes (condensation, coagulation and deposition) as well as ion-aerosol attachment and ion-ion recombination. The formation of particles is treated as model input or, alternatively, the model can be coupled with an existing nucleation model. Ion-UHMA was found to be able to reproduce qualitatively the measured time evolution of the particle number size distribution, when the particle formation and growth rates as well as concentrations of particles > 20 nm in diameter were taken from measurements. The simulated charging state of freshly formed particles during a new particle formation event evolved towards charge equilibrium in line with previously-derived analytical formulae. We provided a few illustrative examples to demonstrate possible applications, to which the Ion-UHMA model could be used in the near future. (orig.)

  8. Estimating marine aerosol particle volume and number from Maritime Aerosol Network data

    Directory of Open Access Journals (Sweden)

    A. M. Sayer

    2012-09-01

    Full Text Available As well as spectral aerosol optical depth (AOD, aerosol composition and concentration (number, volume, or mass are of interest for a variety of applications. However, remote sensing of these quantities is more difficult than for AOD, as it is more sensitive to assumptions relating to aerosol composition. This study uses spectral AOD measured on Maritime Aerosol Network (MAN cruises, with the additional constraint of a microphysical model for unpolluted maritime aerosol based on analysis of Aerosol Robotic Network (AERONET inversions, to estimate these quantities over open ocean. When the MAN data are subset to those likely to be comprised of maritime aerosol, number and volume concentrations obtained are physically reasonable. Attempts to estimate surface concentration from columnar abundance, however, are shown to be limited by uncertainties in vertical distribution. Columnar AOD at 550 nm and aerosol number for unpolluted maritime cases are also compared with Moderate Resolution Imaging Spectroradiometer (MODIS data, for both the present Collection 5.1 and forthcoming Collection 6. MODIS provides a best-fitting retrieval solution, as well as the average for several different solutions, with different aerosol microphysical models. The "average solution" MODIS dataset agrees more closely with MAN than the "best solution" dataset. Terra tends to retrieve lower aerosol number than MAN, and Aqua higher, linked with differences in the aerosol models commonly chosen. Collection 6 AOD is likely to agree more closely with MAN over open ocean than Collection 5.1. In situations where spectral AOD is measured accurately, and aerosol microphysical properties are reasonably well-constrained, estimates of aerosol number and volume using MAN or similar data would provide for a greater variety of potential comparisons with aerosol properties derived from satellite or chemistry transport model data. However, without accurate AOD data and prior knowledge of

  9. Experimental determination of attachment function of radon progeny on aerosol particles

    International Nuclear Information System (INIS)

    Aerosol size information is very important for risk estimation of radon exposure. Size measurements of aerosol particles attaching radon progeny were made by using the Detati's ELPI (Electrical Low Pressure Impactor), and its attachment function was determined. The impactor, which covers a wide size range from 0.03 to 10 μm in diameter, gives number size distribution in real time by an electrical detection method. Prior to those size measurements, effects of impaction substrates on size classification were studied. Tested substrate materials were stainless steel plate and aluminum foil, and those surfaces were as follows: 1) untreated, 2) silicon grease coated, 3) silicon oil coated, 4) adhesive tape stuck. It was suggested that the use of grease- or oil-coated substrates did not interfere for the ELPI's electrical measurements but prevent particle rebound or redispersion. And it was confirmed that the coating gave no damage on alpha energy spectrum analysis by surface-barrier type solid state detector (SSD). Size distribution data on aerosol number and activity were independently taken for each impactor sample. In the size measurements on activity, the correction of sampling loss at the ELPI's charger unit was made. Comparing between number and activity size distributions, attachment function of radon progeny on aerosol surface was estimated. In the lower submicron range, the attachment strongly depend on the aerosol size. The larger the aerosol become, the less the attachment depend on the aerosol size. The attachment function of the submicron aerosols was in a transient region from surface-area proportion to diameter proportion, as shown in the previous studies. It means that the ELPI is useful for measurements on attachment function of radon progeny on aerosol particles. But the ELPI does not demand monodisperse aerosol as carrier aerosol, and the attachment function can be determined for any aerosols in a chamber or field experiment. (author)

  10. Hygroscopicity and chemical composition of Antarctic sub-micrometre aerosol particles and observations of new particle formation

    Directory of Open Access Journals (Sweden)

    E. Asmi

    2010-05-01

    Full Text Available The Antarctic near-coastal sub-micrometre aerosol particle features in summer were characterised based on measured data on aerosol hygroscopicity, size distributions, volatility and chemical ion and organic carbon mass concentrations. Hysplit model was used to calculate the history of the air masses to predict the particle origin. Additional measurements of meteorological parameters were utilised. The hygroscopic properties of particles mostly resembled those of marine aerosols. The measurements took place at 130 km from the Southern Ocean, which was the most significant factor affecting the particle properties. This is explained by the lack of additional sources on the continent of Antarctica. The Southern Ocean was thus a likely source of the particles and nucleating and condensing vapours. The particles were very hygroscopic (HGF 1.75 at 90 nm and very volatile. Most of the sub-100 nm particle volume volatilised below 100 °C. Based on chemical data, particle hygroscopic and volatile properties were explained by a large fraction of non-neutralised sulphuric acid together with organic material. The hygroscopic growth factors assessed from chemical data were similar to measured. Hygroscopicity was higher in dry continental air masses compared with the moist marine air masses. This was explained by the aging of the marine organic species and lower methanesulphonic acid volume fraction together with the changes in the inorganic aerosol chemistry as the aerosol had travelled long time over the continental Antarctica. Special focus was directed in detailed examination of the observed new particle formation events. Indications of the preference of negative over positive ions in nucleation could be detected. However, in a detailed case study, the neutral particles dominated the particle formation process. Freshly nucleated particles had the smallest hygroscopic growth factors, which increased subsequent to particle aging.

  11. Sources markers in aerosols, oceanic particles and sediments

    Directory of Open Access Journals (Sweden)

    Saliot A.

    2009-02-01

    Full Text Available This review presents some diagnostic criteria used for identifying and quantifying terrestrial organic matter inputs to the ocean. Coupled to the isotopic composition of total organic carbon, the analysis of stable biomarkers permits to trace higher plant contributions in aerosols, dusts, sedimenting particles and dissolved phase in the water column and ultimately in recent and ancient sediments and soils. Some applications are presented, based on the analysis of n-alkyl compounds by a combination of gas chromatography and mass spectrometry (n-alkanes, n-alkanols, n-alkanoic acids and wax esters. Another approach has been developed using the analysis of macromolecular compounds present in higher plants. Abundances of the phenolic compounds from lignin, benzene carboxylic acids obtained during cupric oxide oxidation, Curie pyrolysis are used to characterise terrestrial organic matter sources and inputs. Finally due to the importance of biomass burning in continent-ocean transfers, biomarkers are presented in the polycyclic aromatic hydrocarbon class and for monosaccharide derivatives from the breakdown of cellulose.

  12. Sources markers in aerosols, oceanic particles and sediments

    Science.gov (United States)

    Saliot, A.

    2009-02-01

    This review presents some diagnostic criteria used for identifying and quantifying terrestrial organic matter inputs to the ocean. Coupled to the isotopic composition of total organic carbon, the analysis of stable biomarkers permits to trace higher plant contributions in aerosols, dusts, sedimenting particles and dissolved phase in the water column and ultimately in recent and ancient sediments and soils. Some applications are presented, based on the analysis of n-alkyl compounds by a combination of gas chromatography and mass spectrometry (n-alkanes, n-alkanols, n-alkanoic acids and wax esters). Another approach has been developed using the analysis of macromolecular compounds present in higher plants. Abundances of the phenolic compounds from lignin, benzene carboxylic acids obtained during cupric oxide oxidation, Curie pyrolysis are used to characterise terrestrial organic matter sources and inputs. Finally due to the importance of biomass burning in continent-ocean transfers, biomarkers are presented in the polycyclic aromatic hydrocarbon class and for monosaccharide derivatives from the breakdown of cellulose.

  13. Sulfur isotope analyses of individual aerosol particles in the urban aerosol at a central European site (Mainz, Germany

    Directory of Open Access Journals (Sweden)

    B. Winterholler

    2008-05-01

    Full Text Available Sulfur isotope analysis of atmospheric aerosols is a well established tool for identifying sources of sulfur in the atmosphere, estimating emission factors, and tracing the spread of sulfur from anthropogenic sources through ecosystems. Conventional gas mass spectrometry averages the isotopic compositions of several different types of sulfur aerosol particles, and therefore masks the individual isotopic signatures. In contrast, the new single particle technique presented here determines the isotopic signature of the individual particles.

    Primary aerosol particles retain the original isotopic signature of their source. The isotopic composition of secondary sulfates depends on the isotopic composition of precursor SO2 and the oxidation process. The fractionation with respect to the source SO2 is −9‰ for homogeneous and +16.5‰ for heterogeneous oxidation. The sulfur isotope ratio of secondary sulfate particles can therefore be used to identify the oxidation pathway by which this sulfate was formed. With the new single particle technique, different types of primary and secondary sulfates were first identified based on their chemical composition, and then their individual isotopic signature was measured separately. Our samples were collected in Mainz, Germany, in an urban environment. Secondary sulfates (ammonium sulfate, gypsum, mixed sulfates and coatings on silicates or organic aerosol dominated sulfate loadings in our samples. Comparison of the chemical and isotopic composition of secondary sulfates showed that the isotopic composition was homogeneous, independent of the chemical composition. This is typical for particles that derive from in-cloud processing. The isotopic composition of the source SO2 of secondary sulfates was calculated based on the isotopic composition of particles with known oxidation pathway and showed a strong dependence on wind direction. The contribution of heterogeneous

  14. Compact and portable system for evaluation of individual exposure at aerosol particle in urban area

    International Nuclear Information System (INIS)

    A compact and portable system for real-time acquisition of aerosol concentration data in urban and extra-urban area is presented. It is based on two optical type aerosol monitors integrated by aerosol particle separating and collecting devices, assembled into a carrying case together with temperature and relative humidity sensors and a programmable analog data logger; data output is addressed to a dedicated printer or personal computer. Further data about particle size, morphological aspect and particle mass concentration are obtainable by weighing supports used to concurrently collect aerosol particles and/or by means of microanalytical techniques. System performances are evaluated from the point of view of portability, possibility of use as stationary sampler for long-term monitoring purposes and coherence between optical response and ponderal mass. Some tests are finally carried out, to investigate the effect of relative humidity on the optical response of this type of instruments

  15. Radiocarbon analysis in an Alpine ice core: record of anthropogenic and biogenic contributions to carbonaceous aerosols in the past (1650–1940

    Directory of Open Access Journals (Sweden)

    T. M. Jenk

    2006-01-01

    Full Text Available Long-term concentration records of carbonaceous particles (CP are of increasing interest in climate research due to their not yet completely understood effects on climate. Nevertheless, only poor data on their concentrations and sources before the 20th century are available. We present a first long-term record of organic carbon (OC and elemental carbon (EC concentrations – the two main fractions of CP – along with the corresponding fraction of modern carbon (fM derived from radiocarbon (14C analysis in ice. This allows a distinction and quantification of natural (biogenic and anthropogenic (fossil sources in the past. CP were extracted from an ice archive, with resulting carbon quantities in the microgram range. Analysis of 14C by accelerator mass spectrometry (AMS was therefore highly demanding. We analysed 33 samples of 0.4 to 1 kg ice from a 150.5 m long ice core retrieved at Fiescherhorn glacier in December 2002 (46°33'3.2" N, 08°04'0.4" E; 3900 m a.s.l.. Samples were taken from bedrock up to the firn/ice transition, covering the time period 1650–1940 and thus the transition from the pre-industrial to the industrial era. Before ~1850, OC was approaching a purely biogenic origin with a mean concentration of 24 μg kg−1 and a standard deviation of 7 μg kg−1. In 1940, OC concentration was about a factor of 3 higher than this biogenic background, almost half of it originating from anthropogenic sources, i.e. from combustion of fossil fuels. The biogenic EC concentration was nearly constant over the examined time period with 6 μg kg−1 and a standard deviation of 1 μg kg−1. In 1940, the additional anthropogenic input of atmospheric EC was about 50 μg kg−1.

  16. Mixing state of ambient aerosols in Nanjing city by single particle mass spectrometry

    Science.gov (United States)

    Wang, Honglei; An, Junlin; Shen, Lijuan; Zhu, Bin; Xia, Li; Duan, Qing; Zou, Jianan

    2016-05-01

    To investigate the mixing state and size-resolved aerosol in Nanjing, measurements were carried out for the period 14th January-1st February 2013 by using a Single Particle Aerosol Mass Spectrometer (SPAMS). A total of 10,864,766 particles were sized with vacuum aerodynamic diameter (dva) in the range of 0.2-2.0 μm. Of which, 1,989,725 particles were successfully ionized. Aerosol particles employed for analyzing SPAMS data utilized 96% of the hit particles to identify 5 main particle groups. The particle classes include: K-rich particles (K-CN, K-Nitrate, K-Sulfate and K-Secondary), sodium particles, ammonium particles, carbon-rich particles (OC, EC and OCEC) and heavy-metal particles (Fe-Secondary, Pb-Nitrate, Cu-Mn-Secondary and V-Secondary). EC was the largest contributor with a fraction of 21.78%, followed by K-Secondary (17.87%), K-Nitrate (12.68%) and K-CN (11.25%). High particle level and high RH (relative humidity) are two important factors decreasing visibility in Nanjing. Different particle classes have distinct extinction effects. It anti-correlated well with visibility for the K-secondary, sodium, ammonium, EC, Fe-Secondary and K-Nitrate particles. The proportion of EC particles at 0.65-1.4 μm was up to 25% on haze days and was below 10% on clean days.

  17. Mixing state of ambient aerosols in Nanjing city by single particle mass spectrometry

    Science.gov (United States)

    Wang, Honglei; An, Junlin; Shen, Lijuan; Zhu, Bin; Xia, Li; Duan, Qing; Zou, Jianan

    2016-05-01

    To investigate the mixing state and size-resolved aerosol in Nanjing, measurements were carried out for the period 14th January-1st February 2013 by using a Single Particle Aerosol Mass Spectrometer (SPAMS). A total of 10,864,766 particles were sized with vacuum aerodynamic diameter (dva) in the range of 0.2-2.0 μm. Of which, 1,989,725 particles were successfully ionized. Aerosol particles employed for analyzing SPAMS data utilized 96% of the hit particles to identify 5 main particle groups. The particle classes include: K-rich particles (K-CN, K-Nitrate, K-Sulfate and K-Secondary), sodium particles, ammonium particles, carbon-rich particles (OC, EC and OCEC) and heavy-metal particles (Fe-Secondary, Pb-Nitrate, Cu-Mn-Secondary and V-Secondary). EC was the largest contributor with a fraction of 21.78%, followed by K-Secondary (17.87%), K-Nitrate (12.68%) and K-CN (11.25%). High particle level and high RH (relative humidity) are two important factors decreasing visibility in Nanjing. Different particle classes have distinct extinction effects. It anti-correlated well with visibility for the K-secondary, sodium, ammonium, EC, Fe-Secondary and K-Nitrate particles. The proportion of EC particles at 0.65-1.4 μm was up to 25% on haze days and was below 10% on clean days.

  18. Aerosol fluxes and particle growth above managed grassland

    Directory of Open Access Journals (Sweden)

    E. Nemitz

    2009-08-01

    Full Text Available Particle deposition velocities (11–3000 nm diameter measured above grassland by eddy covariance during the EU GRAMINAE experiment in June 2000 averaged 0.24 and 0.03 mm s−1 to long (0.75 m and short (0.07 m grass, respectively. After fertilisation with 108 kg N ha−1 as calcium ammonium nitrate, sustained apparent upward fluxes of particles were observed. Analysis of concentrations and fluxes of potential precursor gases, including NH3, HNO3, HCl and selected VOCs, shows that condensation of HNO3 and NH3 on the surface of existing particles is responsible for this effect. A novel approach is developed to derive particle growth rates at the field scale, from a combination of measurements of vertical fluxes and particle size-distributions. For the first 9 days after fertilization, growth rates of 11 nm particles of 7.04 nm hr−1 and 1.68 nm hr−1 were derived for day and night-time conditions, respectively. This implies total NH4NO3 production rates of 1.11 and 0.44 μg m−3 h−1, respectively. The effect translates into a small error in measured ammonia fluxes (0.06% day, 0.56% night and a large error in NH4+ and NO3 aerosol fluxes of 3.6% and 10%, respectively. By converting rapidly exchanged NH3 and HNO3 into slowly depositing NH4NO3, the reaction modifies the total N budget, though this effect is small (<1% for the 10 days following fertilization, as NH3 emission dominates the net flux. It is estimated that 3.8% of the fertilizer N was volatilised as NH3, of which 0.05% re-condensed to form NH4NO3 particles within the lowest 2 m of the surface layer. This surface induced process would at least scale up to a global NH4NO3 formation of ca. 0.21 kt N yr

  19. Aerosol fluxes and particle growth above managed grassland

    Directory of Open Access Journals (Sweden)

    E. Nemitz

    2009-01-01

    Full Text Available Particle deposition velocities (11–3000 nm diameter measured above grassland by eddy covariance during the EU GRAMINAE experiment in June 2000 averaged 0.24 and 0.03 mm s−1 to long (0.75 m and short (0.07 m grass, respectively. After fertilisation with 108 kg N ha−1 as calcium ammonium nitrate, sustained apparent upward fluxes of particles were observed. Analysis of concentrations and fluxes of potential precursor gases, including NH3, HNO3, HCl and selected VOCs, shows that condensation of HNO3 and NH3 on the surface of existing particles is responsible for this effect. A novel approach is developed to derive particle growth rates at the field scale, from a combination of measurements of vertical fluxes and particle size-distributions. For the first 9 days after fertilization, growth rates of 11 nm particles of 3.5 nm hr−1 and 0.89 nm hr−1 were derived for day and night-time conditions, respectively. This implies total NH4NO3 production rates of 1.1 and 0.44 μg m−3 h−1, respectively. The effect translates into a small error in measured ammonia fluxes (0.06% day, 0.56% night and a larger error in NH4+ and NO3- aerosol fluxes of 3.6% and 10%, respectively. By converting rapidly exchanged NH3 and HNO3 into slowly depositing NH4NO3, the reaction modifies the total N budget, though this effect is small (<1% for the 10 days following fertilization, as NH3 emission dominates the net flux. It is estimated that 3.8% of the fertilizer N was volatilised as NH3, of which 0.05% re-condensed to form NH4NO3 particles within the lowest 2 m of the surface layer. This surface induced process would at least scale up to a global NH4NO3 formation of ca. 0.21 kt N yr

  20. The generation of diesel exhaust particle aerosols from a bulk source in an aerodynamic size range similar to atmospheric particles

    Directory of Open Access Journals (Sweden)

    Daniel J Cooney

    2008-08-01

    Full Text Available Daniel J Cooney1, Anthony J Hickey21Department of Biomedical Engineering; 2School of Pharmacy, University of North Carolina, Chapel Hill, NC, USAAbstract: The influence of diesel exhaust particles (DEP on the lungs and heart is currently a topic of great interest in inhalation toxicology. Epidemiological data and animal studies have implicated airborne particulate matter and DEP in increased morbidity and mortality due to a number of cardiopulmonary diseases including asthma, chronic obstructive pulmonary disorder, and lung cancer. The pathogeneses of these diseases are being studied using animal models and cell culture techniques. Real-time exposures to freshly combusted diesel fuel are complex and require significant infrastructure including engine operations, dilution air, and monitoring and control of gases. A method of generating DEP aerosols from a bulk source in an aerodynamic size range similar to atmospheric DEP would be a desirable and useful alternative. Metered dose inhaler technology was adopted to generate aerosols from suspensions of DEP in the propellant hydrofluoroalkane 134a. Inertial impaction data indicated that the particle size distributions of the generated aerosols were trimodal, with count median aerodynamic diameters less than 100 nm. Scanning electron microscopy of deposited particles showed tightly aggregated particles, as would be expected from an evaporative process. Chemical analysis indicated that there were no major changes in the mass proportion of 2 specific aromatic hydrocarbons (benzo[a]pyrene and benzo[k]fluoranthene in the particles resulting from the aerosolization process.Keywords: diesel exhaust particles, aerosol, inhalation toxicology

  1. Sensitivity of depolarized lidar signals to cloud and aerosol particle properties

    International Nuclear Information System (INIS)

    Measurements from depolarized lidars provide a promising method to retrieve both cloud and aerosol properties and a versatile complement to passive satellite-based sensors. For lidar observations of clouds and aerosols, multiple scattering plays an important role in the scattering process. Monte Carlo simulations are carried out to investigate the sensitivity of lidar backscattering depolarization to cloud and aerosol properties. Lidar parameters are chosen to be similar to those of the upcoming space-based CALIPSO lidar. Cases are considered that consist of a single cloud or aerosol layer, as well as a case in which cirrus clouds overlay different types of aerosols. It is demonstrated that besides thermodynamic cloud phase, the depolarized lidar signal may provide additional information on ice or aerosol particle shapes. However, our results show little sensitivity to ice or aerosol particle sizes. Additionally, for the case of multiple but overlapping layers involving both clouds and aerosols, the depolarized lidar contains information that can help identify the particle properties of each layer

  2. LOAC: a small aerosol optical counter/sizer for ground-based and balloon measurements of the size distribution and nature of atmospheric particles - Part 1: Principle of measurements and instrument evaluation

    Science.gov (United States)

    Renard, Jean-Baptiste; Dulac, François; Berthet, Gwenaël; Lurton, Thibaut; Vignelles, Damien; Jégou, Fabrice; Tonnelier, Thierry; Jeannot, Matthieu; Couté, Benoit; Akiki, Rony; Verdier, Nicolas; Mallet, Marc; Gensdarmes, François; Charpentier, Patrick; Mesmin, Samuel; Duverger, Vincent; Dupont, Jean-Charles; Elias, Thierry; Crenn, Vincent; Sciare, Jean; Zieger, Paul; Salter, Matthew; Roberts, Tjarda; Giacomoni, Jérôme; Gobbi, Matthieu; Hamonou, Eric; Olafsson, Haraldur; Dagsson-Waldhauserova, Pavla; Camy-Peyret, Claude; Mazel, Christophe; Décamps, Thierry; Piringer, Martin; Surcin, Jérémy; Daugeron, Daniel

    2016-04-01

    The study of aerosols in the troposphere and in the stratosphere is of major importance both for climate and air quality studies. Among the numerous instruments available, optical aerosol particles counters (OPCs) provide the size distribution in diameter range from about 100 nm to a few tens of µm. Most of them are very sensitive to the nature of aerosols, and this can result in significant biases in the retrieved size distribution. We describe here a new versatile optical particle/sizer counter named LOAC (Light Optical Aerosol Counter), which is light and compact enough to perform measurements not only at the surface but under all kinds of balloons in the troposphere and in the stratosphere. LOAC is an original OPC performing observations at two scattering angles. The first one is around 12°, and is almost insensitive to the refractive index of the particles; the second one is around 60° and is strongly sensitive to the refractive index of the particles. By combining measurement at the two angles, it is possible to retrieve the size distribution between 0.2 and 100 µm and to estimate the nature of the dominant particles (droplets, carbonaceous, salts and mineral particles) when the aerosol is relatively homogeneous. This typology is based on calibration charts obtained in the laboratory. The uncertainty for total concentrations measurements is ±20 % when concentrations are higher than 1 particle cm-3 (for a 10 min integration time). For lower concentrations, the uncertainty is up to about ±60 % for concentrations smaller than 10-2 particle cm-3. Also, the uncertainties in size calibration are ±0.025 µm for particles smaller than 0.6 µm, 5 % for particles in the 0.7-2 µm range, and 10 % for particles greater than 2 µm. The measurement accuracy of submicronic particles could be reduced in a strongly turbid case when concentration of particles > 3 µm exceeds a few particles cm-3. Several campaigns of cross-comparison of LOAC with other particle counting

  3. Determination of the particle size distribution of aerosols by means of a diffusion battery

    International Nuclear Information System (INIS)

    The different methods allowing to determine the particle size distribution of aerosols by means of diffusion batteries are described. To that purpose, a new method for the processing of experimental data (percentages of particles trapped by the battery vs flow rate) was developed on the basis of calculation principles which are described and assessed. This method was first tested by numerical simulation from a priori particle size distributions and then verified experimentally using a fine uranine aerosol whose particle size distribution as determined by our method was compared with the distribution previously obtained by electron microscopy. The method can be applied to the determination of particle size distribution spectra of fine aerosols produced by 'radiolysis' of atmospheric gaseous impurities. Two other applications concern the detection threshold of the condensation nuclei counter and the 'critical' radii of 'radiolysis' particles

  4. LOAC: a small aerosol optical counter/sizer for ground-based and balloon measurements of the size distribution and nature of atmospheric particles – Part 2: First results from balloon and unmanned aerial vehicle flights

    Directory of Open Access Journals (Sweden)

    J.-B. Renard

    2015-09-01

    Full Text Available In the companion paper (Renard et al., 2015, we have described and evaluated a new versatile optical particle counter/sizer named LOAC (Light Optical Aerosol Counter based on scattering measurements at angles of 12 and 60° that allows some topology identification of particles (droplets, carbonaceous, salts, and mineral dust in addition to size segregated counting in a large diameter range from 0.2 up to possibly more than 100 μm depending on sampling conditions. Its capabilities overpass those of preceding optical particle counters (OPCs allowing the characterization of all kind of aerosols from submicronic-sized absorbing carbonaceous particles in polluted air to very coarse particles (> 10–20 μm in diameter in desert dust plumes or fog and clouds. LOAC's light and compact design allows measurements under all kinds of balloons, on-board unmanned aerial vehicles (UAV and at ground level. We illustrate here the first LOAC airborne results obtained from an unmanned aerial vehicle (UAV and a variety of scientific balloons. The UAV was deployed in a peri-urban environment near Bordeaux in France. Balloon operations include (i tethered balloons deployed in urban environments in Vienna (Austria and Paris (France, (ii pressurized balloons drifting in the lower troposphere over the western Mediterranean (during the Chemistry-Aerosol Mediterranean Experiment – ChArMEx campaigns, (iii meteorological sounding balloons launched in the western Mediterranean region (ChArMEx and from Aire-sur-l'Adour in south-western France (VOLTAIRE-LOAC campaign. More focus is put on measurements performed in the Mediterranean during (ChArMEx and especially during African dust transport events to illustrate the original capability of balloon-borne LOAC to monitor in situ coarse mineral dust particles. In particular, LOAC has detected unexpected large particles in desert sand plumes.

  5. LOAC: a small aerosol optical counter/sizer for ground-based and balloon measurements of the size distribution and nature of atmospheric particles - Part 2: First results from balloon and unmanned aerial vehicle flights

    Science.gov (United States)

    Renard, Jean-Baptiste; Dulac, François; Berthet, Gwenaël; Lurton, Thibaut; Vignelles, Damien; Jégou, Fabrice; Tonnelier, Thierry; Jeannot, Matthieu; Couté, Benoit; Akiki, Rony; Verdier, Nicolas; Mallet, Marc; Gensdarmes, François; Charpentier, Patrick; Mesmin, Samuel; Duverger, Vincent; Dupont, Jean-Charles; Elias, Thierry; Crenn, Vincent; Sciare, Jean; Zieger, Paul; Salter, Matthew; Roberts, Tjarda; Giacomoni, Jérôme; Gobbi, Matthieu; Hamonou, Eric; Olafsson, Haraldur; Dagsson-Waldhauserova, Pavla; Camy-Peyret, Claude; Mazel, Christophe; Décamps, Thierry; Piringer, Martin; Surcin, Jérémy; Daugeron, Daniel

    2016-08-01

    In the companion (Part I) paper, we have described and evaluated a new versatile optical particle counter/sizer named LOAC (Light Optical Aerosol Counter), based on scattering measurements at angles of 12 and 60°. That allows for some typology identification of particles (droplets, carbonaceous, salts, and mineral dust) in addition to size-segregated counting in a large diameter range from 0.2 µm up to possibly more than 100 µm depending on sampling conditions (Renard et al., 2016). Its capabilities overpass those of preceding optical particle counters (OPCs) allowing the characterization of all kind of aerosols from submicronic-sized absorbing carbonaceous particles in polluted air to very coarse particles (> 10-20 µm in diameter) in desert dust plumes or fog and clouds. LOAC's light and compact design allows measurements under all kinds of balloons, on-board unmanned aerial vehicles (UAVs) and at ground level. We illustrate here the first LOAC airborne results obtained from a UAV and a variety of scientific balloons. The UAV was deployed in a peri-urban environment near Bordeaux in France. Balloon operations include (i) tethered balloons deployed in urban environments in Vienna (Austria) and Paris (France), (ii) pressurized balloons drifting in the lower troposphere over the western Mediterranean (during the Chemistry-Aerosol Mediterranean Experiment - ChArMEx campaigns), (iii) meteorological sounding balloons launched in the western Mediterranean region (ChArMEx) and from Aire-sur-l'Adour in south-western France (VOLTAIRE-LOAC campaign). More focus is put on measurements performed in the Mediterranean during (ChArMEx) and especially during African dust transport events to illustrate the original capability of balloon-borne LOAC to monitor in situ coarse mineral dust particles. In particular, LOAC has detected unexpected large particles in desert sand plumes.

  6. LOAC: a small aerosol optical counter/sizer for ground-based and balloon measurements of the size distribution and nature of atmospheric particles - Part 2: First results from balloon and unmanned aerial vehicle flights

    Science.gov (United States)

    Renard, J.-B.; Dulac, F.; Berthet, G.; Lurton, T.; Vignelles, D.; Jégou, F.; Tonnelier, T.; Thaury, C.; Jeannot, M.; Couté, B.; Akiki, R.; Verdier, N.; Mallet, M.; Gensdarmes, F.; Charpentier, P.; Mesmin, S.; Duverger, V.; Dupont, J. C.; Elias, T.; Crenn, V.; Sciare, J.; Giacomoni, J.; Gobbi, M.; Hamonou, E.; Olafsson, H.; Dagsson-Waldhauserova, P.; Camy-Peyret, C.; Mazel, C.; Décamps, T.; Piringer, M.; Surcin, J.; Daugeron, D.

    2015-09-01

    In the companion paper (Renard et al., 2015), we have described and evaluated a new versatile optical particle counter/sizer named LOAC (Light Optical Aerosol Counter) based on scattering measurements at angles of 12 and 60° that allows some topology identification of particles (droplets, carbonaceous, salts, and mineral dust) in addition to size segregated counting in a large diameter range from 0.2 up to possibly more than 100 μm depending on sampling conditions. Its capabilities overpass those of preceding optical particle counters (OPCs) allowing the characterization of all kind of aerosols from submicronic-sized absorbing carbonaceous particles in polluted air to very coarse particles (> 10-20 μm in diameter) in desert dust plumes or fog and clouds. LOAC's light and compact design allows measurements under all kinds of balloons, on-board unmanned aerial vehicles (UAV) and at ground level. We illustrate here the first LOAC airborne results obtained from an unmanned aerial vehicle (UAV) and a variety of scientific balloons. The UAV was deployed in a peri-urban environment near Bordeaux in France. Balloon operations include (i) tethered balloons deployed in urban environments in Vienna (Austria) and Paris (France), (ii) pressurized balloons drifting in the lower troposphere over the western Mediterranean (during the Chemistry-Aerosol Mediterranean Experiment - ChArMEx campaigns), (iii) meteorological sounding balloons launched in the western Mediterranean region (ChArMEx) and from Aire-sur-l'Adour in south-western France (VOLTAIRE-LOAC campaign). More focus is put on measurements performed in the Mediterranean during (ChArMEx) and especially during African dust transport events to illustrate the original capability of balloon-borne LOAC to monitor in situ coarse mineral dust particles. In particular, LOAC has detected unexpected large particles in desert sand plumes.

  7. Comparison between CARIBIC aerosol samples analysed by accelerator-based methods and optical particle counter measurements

    Directory of Open Access Journals (Sweden)

    B. G. Martinsson

    2014-04-01

    Full Text Available Inter-comparison of results from two kinds of aerosol systems in the CARIBIC (Civil Aircraft for the Regular Investigation of the atmosphere Based on an Instrument Container passenger aircraft based observatory, operating during intercontinental flights at 9–12 km altitude, is presented. Aerosol from the lowermost stratosphere (LMS, the extra-tropical upper troposphere (UT and the tropical mid troposphere (MT were investigated. Aerosol particle volume concentration measured with an optical particle counter (OPC is compared with analytical results of the sum of masses of all major and several minor constituents from aerosol samples collected with an impactor. Analyses were undertaken with accelerator-based methods particle-induced X-ray emission (PIXE and particle elastic scattering analysis (PESA. Data from 48 flights during one year are used, leading to a total of 106 individual comparisons. The ratios of the particle volume from the OPC and the total mass from the analyses were in 84% within a relatively narrow interval. Data points outside this interval are connected with inlet-related effects in clouds, large variability in aerosol composition, particle size distribution effects and some cases of non-ideal sampling. Overall, the comparison of these two CARIBIC measurements based on vastly different methods show good agreement, implying that the chemical and size information can be combined in studies of the MT/UT/LMS aerosol.

  8. Determination of Aerosol Particle Diameter in Cementation Room of Radioactive Waste Management Instalation

    International Nuclear Information System (INIS)

    Determination of aerosol particle size distribution has been done using a low pressure cascade impactor with 8-stage metode. The aerosol was sampled with flow rate of 28.3 litre per minute during 4 hours. The counting and calculations result indicated that aerosol particle at compaction room have an aerodynamic median activity diameter (AMAD) between range (2.1 - 3.3) μm. This result could be used for detemine type of filter for contamination level monitoring and estimating the internal radiation level to workers from inhalation. (author)

  9. The effect of viscosity on the HO2 uptake by sucrose and secondary organic aerosol particles

    OpenAIRE

    Lakey, Pascale S. J.; Berkemeier, Thomas; Krapf, Manuel; Dommen, Josef; Steimer, Sarah S.; Whalley, Lisa K.; Ingham, Trevor; Baeza-Romero, Maria T.; Pöschl, Ulrich; Shiraiwa, Manabu; Ammann, Markus; Heard, Dwayne E.

    2016-01-01

    We report the first measurements of HO2 uptake coefficients, γ, for secondary organic aerosol particles (SOA) and for the well-studied model compound sucrose which was doped with copper. Above 65 % relative humidity (RH), γ for copper doped sucrose aerosol particles equalled the surface mass accommodation coefficient α = 0.22 ± 0.06 but decreased to γ = 0.012 ± 0.007 upon decreasing the RH to 17 %. The trend of γ with RH can be explained by an increase in aerosol viscosity, as demonstra...

  10. Transmission electron microscopy study of aerosol particles from the brown hazes in northern China

    Science.gov (United States)

    Li, Weijun; Shao, Longyi

    2009-05-01

    Airborne aerosol collections were performed in urban areas of Beijing that were affected by regional brown haze episodes over northern China from 31 May to 12 June 2007. Morphologies, elemental compositions, and mixing states of 810 individual aerosol particles of different sizes were obtained by transmission electron microscopy coupled with energy-dispersive X-ray spectrometry. The phases of some particles were verified using selected-area electron diffraction. Aerosol particle types less than 10 μm in diameter include mineral, complex secondary (Ca-S, K-, and S-rich), organic, soot, fly ash, and metal (Fe-rich and Zn-bearing). Most soot, fly ash, and organic particles are less than 2 μm in diameter. Approximately 84% of the analyzed mineral particles have diameters between 2 and 10 μm, while 81% of the analyzed complex secondary and metal particles are much smaller, from 0.1 to 2 μm. Trajectory analysis with fire maps show that southerly air masses arriving at Beijing have been transported through many agricultural biomass burning sites and heavy industrial areas. Spherical fly ash and Fe-rich particles were from industrial emissions, and abundant K-rich and organic particles likely originated from field burning of crop residues. Abundant Zn-bearing particles are associated with industrial activities and local waste incinerators. On the basis of the detailed analysis of 443 analyzed aerosol particles, about 70% of these particles are internally mixed with two or more aerosol components from different sources. Most mineral particles are covered with visible coatings that contain N, O, Ca (or Mg), minor S, and Cl. K- and S-rich particles tend to be coagulated with fly ash, soot, metal, and fine-grained mineral particles. Organic materials internally mixed with K- and S-rich particles can be their inclusions and coatings.

  11. The effects of mineral dust particles, aerosol regeneration and ice nucleation parameterizations on clouds and precipitation

    Directory of Open Access Journals (Sweden)

    A. Teller

    2012-03-01

    Full Text Available This study focuses on the effects of aerosol particles on the formation of convective clouds and precipitation in the Eastern Mediterranean sea with a special emphasis on the role of mineral dust particles in these processes. We used a new detailed numerical cloud microphysics scheme that has been implemented in the Weather Research and Forecast (WRF model in order to study aerosol-cloud interaction in 3-D configuration based on realistic meteorological data. Using a number of case studies we tested the contribution of mineral dust particles and different ice nucleation parameterizations to precipitation development. In this study we also investigated the importance of recycled (regenerated aerosols that had been released to the atmosphere following the evaporation of cloud droplets.

    The results showed that increased aerosol concentration due to the presence of mineral dust enhanced the formation of ice crystals. The dynamic evolution of the cloud system sets the time periods and regions in which heavy or light precipitation occurred in the domain. The precipitation rate, the time and duration of precipitation were affected by the aerosol properties only at small area scales (with areas of about 20 km2. Changes of the ice nucleation scheme from ice supersaturation dependent parameterization to a recent approach of aerosol concentration and temperature dependent parameterization modified the ice crystals concentrations but did not affect the total precipitation in the domain. Aerosol regeneration modified the concentration of cloud droplets at cloud base by dynamic recirculation of the aerosols but also had only a minor effect on precipitation.

    The major conclusion from this study is that the effect of mineral dust particles on clouds and total precipitation is limited by the properties of the atmospheric dynamics and the only effect of aerosol on precipitation may come from significant increase in the concentration

  12. Aerosolization, Chemical Characterization, Hygroscopicity and Ice Formation of Marine Biogenic Particles

    Science.gov (United States)

    Alpert, P. A.; Radway, J.; Kilthau, W.; Bothe, D.; Knopf, D. A.; Aller, J. Y.

    2013-12-01

    The oceans cover the majority of the earth's surface, host nearly half the total global primary productivity and are a major source of atmospheric aerosol particles. However, effects of biological activity on sea spray generation and composition, and subsequent cloud formation are not well understood. Our goal is to elucidate these effects which will be particularly important over nutrient rich seas, where microorganisms can reach concentrations of 10^9 per mL and along with transparent exopolymer particles (TEP) can become aerosolized. Here we report the results of mesocosm experiments in which bubbles were generated by two methods, either recirculating impinging water jets or glass frits, in natural or artificial seawater containing bacteria and unialgal cultures of three representative phytoplankton species, Thalassiosira pseudonana, Emiliania huxleyi, and Nannochloris atomus. Over time we followed the size distribution of aerosolized particles as well as their hygroscopicity, heterogeneous ice nucleation potential, and individual physical-chemical characteristics. Numbers of cells and the mass of dissolved and particulate organic carbon (DOC, POC), TEP (which includes polysaccharide-containing microgels and nanogels >0.4 μm in diameter) were determined in the bulk water, the surface microlayer, and aerosolized material. Aerosolized particles were also impacted onto substrates for ice nucleation and water uptake experiments, elemental analysis using computer controlled scanning electron microscopy and energy dispersive analysis of X-rays (CCSEM/EDX), and determination of carbon bonding with scanning transmission X-ray microscopy and near-edge X-ray absorption fine structure spectroscopy (STXM/NEXAFS). Regardless of bubble generation method, the overall concentration of aerosol particles, TEP, POC and DOC increased as concentrations of bacterial and phytoplankton cells increased, stabilized, and subsequently declined. Particles Aerosolized particles were

  13. Metal and silicate particles including nanoparticles are present in electronic cigarette cartomizer fluid and aerosol.

    Directory of Open Access Journals (Sweden)

    Monique Williams

    Full Text Available Electronic cigarettes (EC deliver aerosol by heating fluid containing nicotine. Cartomizer EC combine the fluid chamber and heating element in a single unit. Because EC do not burn tobacco, they may be safer than conventional cigarettes. Their use is rapidly increasing worldwide with little prior testing of their aerosol.We tested the hypothesis that EC aerosol contains metals derived from various components in EC.Cartomizer contents and aerosols were analyzed using light and electron microscopy, cytotoxicity testing, x-ray microanalysis, particle counting, and inductively coupled plasma optical emission spectrometry.The filament, a nickel-chromium wire, was coupled to a thicker copper wire coated with silver. The silver coating was sometimes missing. Four tin solder joints attached the wires to each other and coupled the copper/silver wire to the air tube and mouthpiece. All cartomizers had evidence of use before packaging (burn spots on the fibers and electrophoretic movement of fluid in the fibers. Fibers in two cartomizers had green deposits that contained copper. Centrifugation of the fibers produced large pellets containing tin. Tin particles and tin whiskers were identified in cartridge fluid and outer fibers. Cartomizer fluid with tin particles was cytotoxic in assays using human pulmonary fibroblasts. The aerosol contained particles >1 µm comprised of tin, silver, iron, nickel, aluminum, and silicate and nanoparticles (<100 nm of tin, chromium and nickel. The concentrations of nine of eleven elements in EC aerosol were higher than or equal to the corresponding concentrations in conventional cigarette smoke. Many of the elements identified in EC aerosol are known to cause respiratory distress and disease.The presence of metal and silicate particles in cartomizer aerosol demonstrates the need for improved quality control in EC design and manufacture and studies on how EC aerosol impacts the health of users and bystanders.

  14. Size Resolved Measurements of Springtime Aerosol Particles over the Northern South China Sea

    Science.gov (United States)

    Atwood, Samuel A.; Reid, Jeffrey S.; Kreidenweis, Sonia M.; Cliff, Stephen S.; Zhao, Yongjing; Lin, Neng-Huei; Tsay, Si-Chee; Chu, Yu-Chi; Westphal, Douglas L.

    2012-01-01

    Large sources of aerosol particles and their precursors are ubiquitous in East Asia. Such sources are known to impact the South China Sea (henceforth SCS), a sometimes heavily polluted region that has been suggested as particularly vulnerable to climate change. To help elucidate springtime aerosol transport into the SCS, an intensive study was performed on the remote Dongsha (aka Pratas) Islands Atoll in spring 2010. As part of this deployment, a Davis Rotating-drum Uniform size-cut Monitor (DRUM) cascade impactor was deployed to collect size-resolved aerosol samples at the surface that were analyzed by X-ray fluorescence for concentrations of selected elements. HYSPLIT backtrajectories indicated that the transport of aerosol observed at the surface at Dongsha was occurring primarily from regions generally to the north and east. This observation was consistent with the apparent persistence of pollution and dust aerosol, along with sea salt, in the ground-based dataset. In contrast to the sea-level observations, modeled aerosol transport suggested that the westerly flow aloft (w700 hPa) transported smoke-laden air toward the site from regions from the south and west. Measured aerosol optical depth at the site was highest during time periods of modeled heavy smoke loadings aloft. These periods did not coincide with elevated aerosol concentrations at the surface, although the model suggested sporadic mixing of this free-tropospheric aerosol to the surface over the SCS. A biomass burning signature was not clearly identified in the surface aerosol composition data, consistent with this aerosol type remaining primarily aloft and not mixing strongly to the surface during the study. Significant vertical wind shear in the region also supports the idea that different source regions lead to varying aerosol impacts in different vertical layers, and suggests the potential for considerable vertical inhomogeneity in the SCS aerosol environment.

  15. Low-temperature Bessel beam trap for single submicrometer aerosol particle studies

    Energy Technology Data Exchange (ETDEWEB)

    Lu, Jessica W.; Chasovskikh, Egor; Stapfer, David [Laboratory of Physical Chemistry, ETH Zürich, Vladimir-Prelog-Weg 2, CH-8093 Zürich (Switzerland); Isenor, Merrill; Signorell, Ruth [Laboratory of Physical Chemistry, ETH Zürich, Vladimir-Prelog-Weg 2, CH-8093 Zürich (Switzerland); Department of Chemistry, University of British Columbia, 2036 Main Mall, Vancouver, British Columbia V6T 1Z1 (Canada)

    2014-09-01

    We report on a new instrument for single aerosol particle studies at low temperatures that combines an optical trap consisting of two counter-propagating Bessel beams (CPBBs) and temperature control down to 223 K (−50 °C). The apparatus is capable of capturing and stably trapping individual submicrometer- to micrometer-sized aerosol particles for up to several hours. First results from studies of hexadecane, dodecane, and water aerosols reveal that we can trap and freeze supercooled droplets ranging in size from ∼450 nm to 5500 nm (radius). We have conducted homogeneous and heterogeneous freezing experiments, freezing-melting cycles, and evaporation studies. To our knowledge, this is the first reported observation of the freezing process for levitated single submicrometer-sized droplets in air using optical trapping techniques. These results show that a temperature-controlled CPBB trap is an attractive new method for studying phase transitions of individual submicrometer aerosol particles.

  16. Low-temperature Bessel beam trap for single submicrometer aerosol particle studies

    International Nuclear Information System (INIS)

    We report on a new instrument for single aerosol particle studies at low temperatures that combines an optical trap consisting of two counter-propagating Bessel beams (CPBBs) and temperature control down to 223 K (−50 °C). The apparatus is capable of capturing and stably trapping individual submicrometer- to micrometer-sized aerosol particles for up to several hours. First results from studies of hexadecane, dodecane, and water aerosols reveal that we can trap and freeze supercooled droplets ranging in size from ∼450 nm to 5500 nm (radius). We have conducted homogeneous and heterogeneous freezing experiments, freezing-melting cycles, and evaporation studies. To our knowledge, this is the first reported observation of the freezing process for levitated single submicrometer-sized droplets in air using optical trapping techniques. These results show that a temperature-controlled CPBB trap is an attractive new method for studying phase transitions of individual submicrometer aerosol particles

  17. Particle Characterization and Ice Nucleation Efficiency of Field-Collected Aerosol Particles

    Science.gov (United States)

    Wang, B.; Gilles, M. K.; Laskin, A.; Moffet, R.; Nizkorodov, S.; Roedel, T.; Sterckx, L.; Tivanski, A.; Knopf, D. A.

    2011-12-01

    Atmospheric ice formation by heterogeneous nucleation is one of the least understood processes resulting in cirrus and mixed-phase clouds which affect the global radiation budget, the hydrological cycle, and water vapor distribution. In particular, how organic aerosol affect ice nucleation is not well understood. Here we report on heterogeneous ice nucleation from particles collected during the CalNex campaign at the Caltech campus site, Pasadena, on May 19, 2010 at 6am-12pm (A2) and 12pm-6pm (A3) and May 23 at 6am-12pm (B2) and 6pm-12am (B4). The ice nucleation onsets and water uptake were determined as a function of temperature (200-273 K) and relative humidity with respect to ice (RHice). The ice nucleation efficiency was related to the particle chemical composition. Single particle characterization was provided by using computer controlled scanning electron microscopy with energy dispersive analysis of X-rays (CCSEM/EDX) and scanning transmission X-ray microscopy with near edge X-ray absorption fine structure spectroscopy (STXM/NEXAFS). The STXM/NEXAFS analysis indicates that the morning sample (A2) constitutes organic particles and organic particles with soot and inorganic inclusions. The afternoon sample (A3) is dominated by organic particles with a potentially higher degree of oxidation associated with soot. The B2 sample shows a higher number fraction of magnesium-containing particle indicative of a marine source and ~93% of the particles contained sulfur besides oxygen and carbon as derived from CCSEM/EDX analysis. The B4 sample lacks the strong marine influence and shows higher organic content. Above 230 K, we observed water uptake followed by condensation freezing at mean RH of 93-100% and 89-95% for A2 and A3, respectively. This indicates that the aged A3 particles are efficient ice nuclei (IN) for condensation freezing. Below 230 K A2 and A3 induced deposition ice nucleation between 125-155% RHice (at mean values of 134-150% RHice). The B2 and B4

  18. SPM analysis on groups of single aerosol particles around steel plant

    Institute of Scientific and Technical Information of China (English)

    沙因; 王安璞; 等

    1996-01-01

    Several methods for preparing samples of dispersed single aeroslo particles used in scanning proton microprobe(SPM) analysis were tested.Many elements such as Al,Si,S,Cl,Ca,Ti,Cr,Mn,Fe,Ni,Cu and Zn in the groups of different single aerosol particles from the Capital Steel Plant area were analyzed by SPM,The distributions of elemental contents in the group of single particles were mapped with three dimensional contour and the isometric.A new approach to study the group of different single aerosol particles for air pollution is developed in the present work.The results are significant to assessing the environmental impact of the dispersed single aerosol particles.

  19. Hygroscopic growth of urban aerosol particles during the 2009 Mirage-Shanghai Campaign

    Science.gov (United States)

    Ye, Xingnan; Tang, Chen; Yin, Zi; Chen, Jianmin; Ma, Zhen; Kong, Lingdong; Yang, Xin; Gao, Wei; Geng, Fuhai

    2013-01-01

    The hygroscopic properties of submicrometer urban aerosol particles were studied during the 2009 Mirage-Shanghai Campaign. The urban aerosols were composed of more-hygroscopic and nearly-hydrophobic particles, together with a trace of less-hygroscopic particles. The mean hygroscopicity parameter κ of the more-hygroscopic mode varied in the range of 0.27-0.39 depending on particle size. The relative abundance of the more-hygroscopic particles at any size was ca. 70%, slightly increasing with particle size. The number fraction of the nearly-hydrophobic particles fluctuated between 0.1 and 0.4 daily, in accordance with traffic emissions and atmospheric diffusion. The results from relative humidity dependence on hygroscopic growth and chemical analysis of fine particles indicated that particulate nitrate formation through the homogenous gas-phase reaction was suppressed under ammonia-deficient atmosphere in summer whereas the equilibrium was broken by more available NH3 during adverse meteorological conditions.

  20. Direct observation of aerosol particles in aged agricultural biomass burning plumes impacting urban atmospheres

    Directory of Open Access Journals (Sweden)

    W. Y. Li

    2010-04-01

    Full Text Available Emissions from agricultural biomass burning (ABB in northern China have a significant impact on the regional and the global climate. According to the Giovanni's Aerosol optical depth (AOD map, the monthly average AOD at 550 nm in northern China in 2007 shows a maximum value of 0.7 in June, suggesting that episodes of severe aerosol pollution occurred in this region. Aerosol particles were collected in urban Beijing during regional brown hazes from 12 to 30 June, 2007. Transmission electron microscopy with energy-dispersive X-ray spectrometry characterized the morphology, composition, and mixing state of aerosol particles. Potassium salts (K2SO4 and KNO3, ammonium sulfate, soot, and organic particles predominated in fine particles (diameter <1 μm collected from 12 to 20 June, 2007. In contrast, from 21 to 30 June, 2007, ammonium sulfate, soot, and organic particles were dominant. Potassium-dominant particles as a tracer of biomass burning, together with wildfire maps, show that intensive regional ABB in northern China from 10 to 20 June, 2007 contributed significantly to the regional haze. After long-range transport, ABB particles exhibited marked changes in their morphology, elemental composition, and mixing state. Heterogeneous reactions completely converted KCl particles from ABB into K2SO4 and KNO3. Soot particles were generally mixed with potassium salts, ammonium salts, and organic particles. In addition, the abundant aged organic particles and soluble salts emitted by ABB become more hygroscopic and increase their size during long-range transport, becoming in effect additional cloud condensation nuclei. The high AOD (average value at 2.2 during 12 to 20 June, 2007, in Beijing is partly explained by the hygroscopic growth of aged fine aerosol particles and by the strong absorption of internally mixed soot particles, both coming from regional ABB emissions.

  1. Heterogeneous nucleation of ice particles on glassy aerosols modifies TTL cirrus

    Science.gov (United States)

    Wilson, T. W.; Murray, B. J.; Dobbie, S.; Al-Jumur, S. M.; Cui, Z.; Wagner, R.; Moehler, O.; Schnaiter, M.; Benz, S.; Niemand, M.; Saathoff, H.; Skrotzki, J.; Ebert, V.; Wagner, S.; Karcher, B.

    2010-12-01

    Experiments at the AIDA chamber, Karlsruhe Institute of Technology, have shown that glassy aqueous citric acid aerosol can nucleate ice at temperatures relevant to the tropical tropopause layer (TTL)(1). Modelling suggests this new route to the formation of TTL cirrus can provide an explanation for the very low ice particle number density observed in cirrus clouds in this region and may lead to high in-cloud supersaturations(1). Nucleation of ice on glassy aerosol is consistent with the absence of traditional ice nuclei in sampled TTL cirrus residue(2). In addition, we will present new data from experiments performed in July 2010 at the AIDA chamber using glassy aerosols composed of other atmospherically relevant compounds (levoglucosan, raffinose) and an internal mixture of five dicarboxylic acids and ammonium sulphate (raffinose/M5AS)(3). All four systems tested nucleate ice when in a glassy state. This indicates that heterogeneous ice nucleation is a general property of glassy aerosols and that natural aerosols which are composed of similar molecules will also nucleate ice if glassy. Glassy aqueous levoglucosan and raffinose/M5AS aerosol nucleated ice at temperatures similar to those found for glassy aqueous citric acid aerosol (<202 K). Whereas raffinose, which forms a glass at much higher temperatures, nucleated ice heterogeneously at up to ~220 K. This activity at higher temperatures suggests that ice nucleation by glassy aerosol may also play a role in the formation of warmer ice clouds. (1)B. J. Murray et al., Heterogeneous nucleation of ice particles on glassy aerosols under cirrus conditions, Nature Geosci, 2010, 3, 233-237. (2)K. D. Froyd et al., Aerosols that form subvisible cirrus at the tropical tropopause, Atmos. Chem. Phys., 2010, 10, 209-218. (3)B. Zobrist et al., Do atmospheric aerosols form glasses?, Atmos. Chem. Phys., 2008, 8, 5221-5244.

  2. Formation of highly porous aerosol particles by atmospheric freeze-drying in ice clouds

    Science.gov (United States)

    Rudich, Yinon; Adler, Gabriela; Koop, Thomas; Taraniuk, Ilya; Moise, Tamar; Koren, Ilan; Heiblum, Reuven; Haspel, Carynelisa

    2014-05-01

    In cold high altitude cirrus clouds and anvils of high convective clouds in the tropics and mid-latitudes, ice partciles that are exposed to subsaturation conditions with respect to ice can sublimate, leaving behind residual modified aerosols. This freeze-drying process can occur in various types of clouds. In this talk we will describe experiements that simulate the atmospheric freeze-drying cycle of aerosols. We find that aerosols with high organic content can form highly porous particles (HPA) with a larger diameter and a lower density than the initial homogenous aerosol following ice subliation. We attribute this morphology change to phase separation upon freezing followed by a glass transition of the organic material that can preserve a porous structure follwoing ice sublimation. We find that the highly porous aerosol scatter solar light less efficiently than non-porous aerosol particles. A porous structure may explain the previously observed enhancement in ice nucleation efficiency of glassy organic particles. These observations may have implications for subsequent cloud formation cycles and aerosol albedo near cloud edges.

  3. The importance of interstitial particle scavenging by cloud droplets in shaping the remote aerosol size distribution and global aerosol-climate effects

    Directory of Open Access Journals (Sweden)

    J. R. Pierce

    2015-02-01

    Full Text Available In this paper, we investigate the coagulation of interstitial aerosol particles (particles too small to activate to cloud droplets with cloud drops, a process often ignored in aerosol-climate models. We use the GEOS-Chem-TOMAS global chemical transport model with aerosol microphysics to calculate the changes in the aerosol size distribution, cloud-albedo aerosol indirect effect, and direct aerosol effect due to the interstitial coagulation process. We find that inclusion of interstitial coagulation in clouds lowers total particle number concentrations by 15–21% globally, where the range is due to varying assumptions regarding activation diameter, cloud droplet size, and ice cloud physics. The interstitial coagulation process lowers the concentration of particles with dry diameters larger than 80 nm (a proxy for larger CCN by 10–12%. These 80 nm particles are not directly removed by the interstitial coagulation, but are reduced in concentration because fewer smaller particles grow to diameters larger than 80 nm. The global aerosol indirect effect of adding interstitial coagulation varies from +0.4 to +1.3 W m−2 where again the range depends on our cloud assumptions. Thus, the aerosol indirect effect of this process is significant, but the magnitude depends greatly on assumptions regarding activation diameter, cloud droplet size, and ice cloud physics. The aerosol direct effect of interstitial coagulation process is minor (−2 due to the shift in the aerosol size distribution at sizes where scattering is most effective being small. We recommend that this interstitial scavenging process be considered in aerosol models when the size distribution and aerosol indirect effects are important.

  4. NUMBER CONCENTRATION, SIZE DISTRIBUTION AND FINE PARTICLE FRACTION OF TROPOSPHERIC AND STRATOSPHERIC AEROSOLS

    Institute of Scientific and Technical Information of China (English)

    Li Xu; Guangyu Shi; Li Zhang; Jun Zhou; Yasunobu Iwasaka

    2003-01-01

    Aerosol observations were carried out at Xianghe Scientific Balloon Base (39.45°N, 117°E) using a stratospheric balloon. The particle number concentrations of the tropospheric and stratospheric aerosols were directly explored.The vertical distributions of the number concentration, number-size (that is, particle number versus particle size)distribution, and the fraction of fine particles (0.5 μm>r>0.15 μm/r>0.15 μm) are reported in this paper. The profiles of particle concentration present multi-peak phenomenon. The pattern of size distribution for atmospheric aerosol indicates a tri-modal (r=~0.2 μm, ~0.88 μm and ~7.0 μm) and a bi-modal (r=~0.13 μm and 2.0 μm). The number-size distribution almost fits the Junge distribution for particles with r<0.5 μm in the stratosphere of 1993 and the troposphere of 1994. But the distributions of coarse particles (r>0.5 μm) are not uniform. The number-size distribution exhibits also a wide size range in the troposphere of 1993. The results demonstrate that fine particles represent the major portion in the troposphere during the measurement period, reaching as high as 95% in 1994. Certain coarse particle peaks in the troposphere were attributed to clouds and other causes, and in the stratosphere to volcanic eruption. The stratospheric aerosol layer consists of unique fractions of fine or coarse particles depending on their sources. In summary, the process of gas-to-particles conversion was active and the coarse particles were rich over the Xianghe area. The measurements also demonstrate that the spatial and temporal atmospheric aerosol distributions are nonuniform and changeful.

  5. Elemental composition of aerosol particles from two atmospheric monitoring stations in the Amazon Basin

    International Nuclear Information System (INIS)

    One key region for the study of processes that are changing the composition of the global atmosphere is the Amazon Basin tropical rain forest. The high rate of deforestation and biomass burning is emitting large amounts of gases and fine-mode aerosol particles to the global atmosphere. Two background monitoring stations are operating continuously measuring aerosol composition, at Cuiaba, and Serra do Navio. Fine- and coarse-mode aerosol particles are being collected using stacked filter units. Particle induced X-ray emission (PIXE) was used to measure concentrations of up to 21 elements: Al, Si, P, S, Cl, K, Ca, Ti, V, Cr, Mn, Fe, Ni, Cu, Zn, Se, Br, Rb, Sr, Zr, and Pb. The elemental composition was measured at the new PIXE facility from the University of Sao Paulo, using a dedicated 5SDH tandem Pelletron nuclear accelerator. Absolute principal factor analysis (APFA) has derived absolute elemental source profiles. At the Serra do Navio sampling site a very clean background aerosol is being observed. Biogenic aerosol dominates the fine-mode mass concentration, with the presence of K, P, S, Cl, Zn, Br, and FPM. Three components dominate the aerosol composition: Soil dust particles, the natural biogenic release by the forest, and a marine aerosol component. At the Cuiaba site, during the dry season, a strong component of biomass burning is observed. An aerosol mass concentration up to 120 μg/m3 was measured. APFA showed three components: Soil dust (Al, Ca, Ti, Mn, Fe), biomass burning (soot, FPM, K, Cl) and natural biogenic particles (K, S, Ca, Mn, Zn). The fine-mode biogenic component of both sites shows remarkable similarities, although the two sampling sites are 3000 km apart. Several essential plant nutrients like P, K, S, Ca, Ni and others are transported in the atmosphere as a result of biomass burning processes. (orig.)

  6. Characterization of a Quadrotor Unmanned Aircraft System for Aerosol-Particle-Concentration Measurements.

    Science.gov (United States)

    Brady, James M; Stokes, M Dale; Bonnardel, Jim; Bertram, Timothy H

    2016-02-01

    High-spatial-resolution, near-surface vertical profiling of atmospheric chemical composition is currently limited by the availability of experimental platforms that can sample in constrained environments. As a result, measurements of near-surface gradients in trace gas and aerosol particle concentrations have been limited to studies conducted from fixed location towers or tethered balloons. Here, we explore the utility of a quadrotor unmanned aircraft system (UAS) as a sampling platform to measure vertical and horizontal concentration gradients of trace gases and aerosol particles at high spatial resolution (1 m) within the mixed layer (0-100 m). A 3D Robotics Iris+ autonomous quadrotor UAS was outfitted with a sensor package consisting of a two-channel aerosol optical particle counter and a CO2 sensor. The UAS demonstrated high precision in both vertical (±0.5 m) and horizontal positions (±1 m), highlighting the potential utility of quadrotor UAS drones for aerosol- and trace-gas measurements within complex terrain, such as the urban environment, forest canopies, and above difficult-to-access areas such as breaking surf. Vertical profiles of aerosol particle number concentrations, acquired from flights conducted along the California coastline, were used to constrain sea-spray aerosol-emission rates from coastal wave breaking. PMID:26730457

  7. Hygroscopicity of aerosol particles and CCN activity of nearly hydrophobic particles in the urban atmosphere over Japan during summer

    Science.gov (United States)

    Ogawa, Shuhei; Setoguchi, Yoshitaka; Kawana, Kaori; Nakayama, Tomoki; Ikeda, Yuka; Sawada, Yuuki; Matsumi, Yutaka; Mochida, Michihiro

    2016-06-01

    We investigated the hygroscopicity of 150 nm particles and the number-size distributions and the cloud condensation nuclei (CCN) activity of nearly hydrophobic particles in aerosols over Nagoya, Japan, during summer. We analyzed the correlations between the number concentrations of particles in specific hygroscopic growth factor (g) ranges and the mass concentrations of chemical components. This analysis suggests the association of nearly hydrophobic particles with hydrocarbon-like organic aerosol, elemental carbon and semivolatile oxygenated organic aerosol (SV-OOA), that of less hygroscopic particles with SV-OOA and nitrate and that of more hygroscopic particles with low-volatile oxygenated organic aerosol (LV-OOA) and sulfate. The hygroscopicity parameter (κ) of organics was derived based on the g distributions and chemical composition of 150 nm particles. The κ of the organics correlated positively with the fraction of the total organic mass spectral signal at m/z 44 and the volume fraction of the LV-OOA to the organics, indicating that organics with highly oxygenated structures including carboxylic acid groups contribute to the water uptake. The number-size distributions of the nearly hydrophobic particles with g around 1.0 and 1.1 correlated with the mass concentrations of chemical components. The results show that the chemical composition of the particles with g around 1.0 was different between the Aitken mode and the accumulation mode size ranges. An analysis for a parameter Fmax of the curves fitted to the CCN efficiency spectra of the particles with g around 1.0 suggests that the coating by organics associated with SV-OOA elevated the CCN activity of these particles.

  8. Aerosolization, Chemical Characterization, Hygroscopicity and Ice Formation of Marine Biogenic Particles

    Science.gov (United States)

    Alpert, P. A.; Radway, J.; Kilthau, W.; Bothe, D.; Knopf, D. A.; Aller, J. Y.

    2013-12-01

    The oceans cover the majority of the earth's surface, host nearly half the total global primary productivity and are a major source of atmospheric aerosol particles. However, effects of biological activity on sea spray generation and composition, and subsequent cloud formation are not well understood. Our goal is to elucidate these effects which will be particularly important over nutrient rich seas, where microorganisms can reach concentrations of 10^9 per mL and along with transparent exopolymer particles (TEP) can become aerosolized. Here we report the results of mesocosm experiments in which bubbles were generated by two methods, either recirculating impinging water jets or glass frits, in natural or artificial seawater containing bacteria and unialgal cultures of three representative phytoplankton species, Thalassiosira pseudonana, Emiliania huxleyi, and Nannochloris atomus. Over time we followed the size distribution of aerosolized particles as well as their hygroscopicity, heterogeneous ice nucleation potential, and individual physical-chemical characteristics. Numbers of cells and the mass of dissolved and particulate organic carbon (DOC, POC), TEP (which includes polysaccharide-containing microgels and nanogels >0.4 μm in diameter) were determined in the bulk water, the surface microlayer, and aerosolized material. Aerosolized particles were also impacted onto substrates for ice nucleation and water uptake experiments, elemental analysis using computer controlled scanning electron microscopy and energy dispersive analysis of X-rays (CCSEM/EDX), and determination of carbon bonding with scanning transmission X-ray microscopy and near-edge X-ray absorption fine structure spectroscopy (STXM/NEXAFS). Regardless of bubble generation method, the overall concentration of aerosol particles, TEP, POC and DOC increased as concentrations of bacterial and phytoplankton cells increased, stabilized, and subsequently declined. Particles cloud formation and potential

  9. Investigation of Aerosol Surface Area Estimation from Number and Mass Concentration Measurements: Particle Density Effect

    Science.gov (United States)

    Ku, Bon Ki; Evans, Douglas E.

    2015-01-01

    For nanoparticles with nonspherical morphologies, e.g., open agglomerates or fibrous particles, it is expected that the actual density of agglomerates may be significantly different from the bulk material density. It is further expected that using the material density may upset the relationship between surface area and mass when a method for estimating aerosol surface area from number and mass concentrations (referred to as “Maynard’s estimation method”) is used. Therefore, it is necessary to quantitatively investigate how much the Maynard’s estimation method depends on particle morphology and density. In this study, aerosol surface area estimated from number and mass concentration measurements was evaluated and compared with values from two reference methods: a method proposed by Lall and Friedlander for agglomerates and a mobility based method for compact nonspherical particles using well-defined polydisperse aerosols with known particle densities. Polydisperse silver aerosol particles were generated by an aerosol generation facility. Generated aerosols had a range of morphologies, count median diameters (CMD) between 25 and 50 nm, and geometric standard deviations (GSD) between 1.5 and 1.8. The surface area estimates from number and mass concentration measurements correlated well with the two reference values when gravimetric mass was used. The aerosol surface area estimates from the Maynard’s estimation method were comparable to the reference method for all particle morphologies within the surface area ratios of 3.31 and 0.19 for assumed GSDs 1.5 and 1.8, respectively, when the bulk material density of silver was used. The difference between the Maynard’s estimation method and surface area measured by the reference method for fractal-like agglomerates decreased from 79% to 23% when the measured effective particle density was used, while the difference for nearly spherical particles decreased from 30% to 24%. The results indicate that the use of

  10. Real-time detection of individual secondary organic aerosol particle from photooxidation of toluene using aerosol time of flight mass spectrometer

    Institute of Scientific and Technical Information of China (English)

    WANG Zhenya; HAO Liqing; ZHOU Liuzhu; GUO Xiaoyong; ZHAO Wenwu; FANG Li; ZHANG Weijun

    2006-01-01

    Photooxidation of the aromatic hydrocarbon toluene and its subsequent reactions were carried out using UV-irradiation of toluene/CH3ONO/NO/air mixtures in a home-made smog chamber.The secondary organic aerosols could be formed after those oxidation products of semi-volatile or-ganic compounds were partitioned between gas phase and particle phase. The aerosol time of flight mass spectrometer (ATOFMS) was used to measure size and molecular composition of individual secondary organic aerosol particle. Size distribution and chemical composition of secondary organic aerosol were got in real time.

  11. Glyoxal processing by aerosol multiphase chemistry: towards a kinetic modeling framework of secondary organic aerosol formation in aqueous particles

    Directory of Open Access Journals (Sweden)

    B. Ervens

    2010-09-01

    Full Text Available This study presents a modeling framework based on laboratory data to describe the kinetics of glyoxal reactions that form secondary organic aerosol (SOA in aqueous aerosol particles. Recent laboratory results on glyoxal reactions are reviewed and a consistent set of empirical reaction rate constants is derived that captures the kinetics of glyoxal hydration and subsequent reversible and irreversible reactions in aqueous inorganic and water-soluble organic aerosol seeds. Products of these processes include (a oligomers, (b nitrogen-containing products, (c photochemical oxidation products with high molecular weight. These additional aqueous phase processes enhance the SOA formation rate in particles and yield two to three orders of magnitude more SOA than predicted based on reaction schemes for dilute aqueous phase (cloud chemistry for the same conditions (liquid water content, particle size.

    The application of the new module including detailed chemical processes in a box model demonstrates that both the time scale to reach aqueous phase equilibria and the choice of rate constants of irreversible reactions have a pronounced effect on the predicted atmospheric relevance of SOA formation from glyoxal. During day time, a photochemical (most likely radical-initiated process is the major SOA formation pathway forming ∼5 μg m−3 SOA over 12 h (assuming a constant glyoxal mixing ratio of 300 ppt. During night time, reactions of nitrogen-containing compounds (ammonium, amines, amino acids contribute most to the predicted SOA mass; however, the absolute predicted SOA masses are reduced by an order of magnitude as compared to day time production. The contribution of the ammonium reaction significantly increases in moderately acidic or neutral particles (5 < pH < 7.

    Glyoxal uptake into ammonium sulfate seed under dark conditions can be represented with a single reaction parameter keffupt that does not depend

  12. Aerosol particle size does not predict pharmacokinetic determined lung dose in children

    DEFF Research Database (Denmark)

    Bønnelykke, Klaus; Chawes, Bo L K; Vindfeld, Signe;

    2013-01-01

    In vitro measures of aerosol particles size, such as the fine particle mass, play a pivotal role for approval of inhaled anti-asthmatic drugs. However, the validity as a measure of dose to the lungs in children lacks evidence. In this study we investigated for the first time the association between...... was assessed after single inhalation. The corresponding emitted mass of drug in segments of aerosol particle size was assessed ex vivo by replicating the inhalation flows recorded by transducers built into the Diskus® inhaler and re-playing them in a breathing simulator. There was no correlation between any...... of drug delivery to the lung....

  13. An overview of differential mobility analyzers for size classification of nanometer-sized aerosol particles

    Directory of Open Access Journals (Sweden)

    Nakorn Tippayawong

    2008-03-01

    Full Text Available Size classification of nanoparticles is an important process in the electrical mobility particle size analyzer. The differential mobility analyzer (DMA is one of the most commonly used devices for classifying and measuring nanometersized aerosol particles between 1 nm to 1 μm in diameter, based on their electrical mobility. The DMA can be described as an assembly of two concentrically cylindrical electrodes with an air gap between the walls. In the DMA, air and aerosol flows enter from one end, pass through the annulus and exit the other end. An electric field is applied between the inner and outer electrodes. Particles having a specific mobility exit with the monodisperse air flow through a small slit located at the bottom of the inner electrode. These particles are transferred to a particle counter to determine the particle number concentration. In the past several decades, there have been numerous extensive studies and developments on the DMA. Nonetheless, they are different in terms of specific applications, construction, particle size range, as well as time response and resolution. The purpose of this article is to provide an overview of the state-of-the-art existing cylindrical DMAs for aerosol particle size classification as well as for the generation of monodisperse aerosol in nanometer size range. A description of the operating principles, detailed physical characteristics of these DMAs, including the single-channel and multi-channel DMAs, as well as some examples of applications to nanotechnology are given.

  14. Tire-tread and bitumen particle concentrations in aerosol and soil samples

    DEFF Research Database (Denmark)

    Fauser, Patrik; Tjell, Jens Christian; Mosbæk, Hans;

    2002-01-01

    ire and bitumen particle concentrations are determined in aerosol and soil samples. They each constitute about 5 wt-% of the total suspended particulate matter (TSP) in inner city air, collected with a Berner low pressure impactor, 5 m from a road. The particle size distribution shows that 92% of...

  15. Quantification of bitumen particles in aerosol and soil samples using HP-GPC

    DEFF Research Database (Denmark)

    Fauser, Patrik; Tjell, Jens Christian; Mosbæk, Hans;

    2000-01-01

    A method for identifying and quantifying bitumen particles, generated from the wear of roadway asphalts, in aerosol and soil samples has been developed. Bitumen is found to be the only contributor to airborne particles containing organic molecules with molecular weights larger than 2000 g pr. mol...

  16. Measurement of overall uptake coefficients for HO2 radicals by aerosol particles sampled from ambient air at Mts. Tai and Mang, China

    OpenAIRE

    H. Akimoto; Z. Wang; K. Okuzawa; K. Kawamura; Li, J.; Liu, Y; P. Pochanart; Taketani, F.; Y. Kanaya

    2012-01-01

    HO2 uptake coefficients for ambient aerosol particles, collected on quartz filter using a high-volume air sampler in China, were measured using an aerosol flow tube coupled with a chemical conversion/laser-induced fluorescence technique at 760 Torr and 298 K, with a relative humidity of 75%. Aerosol particles were regenerated with an atomizer using the water extracts from the aerosol particles. Over 10 samples, the measured HO2 uptake coefficients for the aerosol particles at the Mt. ...

  17. Particle generation methods applied in large-scale experiments on aerosol behaviour and source term studies

    International Nuclear Information System (INIS)

    In aerosol research aerosols of known size, shape, and density are highly desirable because most aerosols properties depend strongly on particle size. However, such constant and reproducible generation of those aerosol particles whose size and concentration can be easily controlled, can be achieved only in laboratory-scale tests. In large scale experiments, different generation methods for various elements and compounds have been applied. This work presents, in a brief from, a review of applications of these methods used in large scale experiments on aerosol behaviour and source term. Description of generation method and generated aerosol transport conditions is followed by properties of obtained aerosol, aerosol instrumentation used, and the scheme of aerosol generation system-wherever it was available. An information concerning aerosol generation particular purposes and reference number(s) is given at the end of a particular case. These methods reviewed are: evaporation-condensation, using a furnace heating and using a plasma torch; atomization of liquid, using compressed air nebulizers, ultrasonic nebulizers and atomization of liquid suspension; and dispersion of powders. Among the projects included in this worked are: ACE, LACE, GE Experiments, EPRI Experiments, LACE-Spain. UKAEA Experiments, BNWL Experiments, ORNL Experiments, MARVIKEN, SPARTA and DEMONA. The aim chemical compounds studied are: Ba, Cs, CsOH, CsI, Ni, Cr, NaI, TeO2, UO2Al2O3, Al2SiO5, B2O3, Cd, CdO, Fe2O3, MnO, SiO2, AgO, SnO2, Te, U3O8, BaO, CsCl, CsNO3, Urania, RuO2, TiO2, Al(OH)3, BaSO4, Eu2O3 and Sn. (Author)

  18. Fluorescence from atmospheric aerosol detected by a lidar indicates biogenic particles in the lowermost stratosphere

    Directory of Open Access Journals (Sweden)

    F. Immler

    2005-01-01

    Full Text Available With a lidar system that was installed in Lindenberg/Germany, we observed in June 2003 an extended aerosol layer at 13km altitude in the lowermost stratosphere. This layer created an inelastic backscatter signal that we detected with a water vapour Raman channel, but that was not produced by Raman scattering. Also, we find evidence for inelastic scattering from a smoke plume from a forest fire that we observed in the troposphere. We interpret the unexpected properties of these aerosols as fluorescence induced by the laser beam at organic components of the aerosol particles. Fluorescence from ambient aerosol had not yet been considered detectable by lidar systems. However, organic compounds such as polycyclic aromatic hydrocarbons sticking to the aerosol particles, or bioaerosol such as bacteria, spores or pollen fluoresce when excited with UV-radiation in a way that is detectable by our lidar system. Therefore, we conclude that fluorescence from organic material released by biomass burning creates, inelastic backscatter signals that we measured with our instrument and thus demonstrate a new and powerful way to characterize aerosols by a remote sensing technique. The stratospheric aerosol layer that we have observed in Lindenberg for three consecutive days is likely to be a remnant from Siberian forest fire plumes lifted across the tropopause and transported around the globe.

  19. The formation of aerosol particles during combustion of biomass and waste. Final report

    Energy Technology Data Exchange (ETDEWEB)

    Hjerrild Zeuthen, J.

    2007-05-15

    This thesis describes the formation of aerosol particles during combustion of biomass and waste. The formation of aerosol particles is investigated by studying condensation of alkali salts from synthetic flue gasses in a laboratory tubular furnace. In this so-called laminar flow aerosol condenser-furnace gaseous alkali chlorides are mixed with sulphur dioxide, water vapour and oxygen. At high temperatures the alkali chloride reacts with sulphur dioxide to form alkali sulphate. During subsequent cooling of the synthetic flue gas the chlorides and sulphates condense either as deposits on walls or on other particles or directly from the gas phase by homogenous nucleation. A previously developed computer code for simulation of one-component nucleation of particles in a cylindrical laminar flow is extended to include a homogeneous gas phase reaction to produce gaseous alkali sulphate. The formation of aerosol particles during full-scale combustion of wheat straw is investigated in a 100 MW grate-fired boiler. Finally, aerosols from incineration of waste are investigated during full-scale combustion of municipal waste in a 22 MW grate-fired unit. (BA)

  20. A study of particle deposition in ducts - Optimisation of aerosol sampling pipes

    International Nuclear Information System (INIS)

    The scope of this study was the optimisation of radioactive aerosol measurement, which is often carried out after the aerosol transport through pipes. The main physical laws governing aerosols and the basis of fluid mechanics are first recalled; the various data scattered in the literature on the deposition process of particles in ducts were gathered together. A slightly turbulent flow regime propitious to aerosol transfer was defined by in situ and laboratory experiments. Thanks to the great sensitivity of the method used to measure the deposition of fluorescent aerosols, a systematic experimental investigation was undertaken. The size of the monodisperse particles ranged from 10-2 to 10 μm, and their electrical charge state was made variable. The validity of the equations available for particle deposition in a laminar flow was verified and attempts were made to fill in the gaps on turbulent flow. For the optimal flow regime a set of simple equations was developed in order to forecast the deposition of particles of any size, any electrical charge, in any straight or bent horizontal or vertical cylindrical duct with conducting smooth walls. In the case of charged particles, the effects of roughness and insulating walls were studied

  1. Stratospheric aerosol particle size information in Odin-OSIRIS limb scatter spectra

    Science.gov (United States)

    Rieger, L. A.; Bourassa, A. E.; Degenstein, D. A.

    2014-02-01

    The Optical Spectrograph and InfraRed Imaging System (OSIRIS) onboard the Odin satellite has now taken over a decade of limb scatter measurements that have been used to retrieve the version 5 stratospheric aerosol extinction product. This product is retrieved using a representative particle size distribution to calculate scattering cross sections and scattering phase functions for the forward model calculations. In this work the information content of OSIRIS measurements with respect to stratospheric aerosol is systematically examined for the purpose of retrieving particle size information along with the extinction coefficient. The benefit of using measurements at different wavelengths and scattering angles in the retrieval is studied, and it is found that incorporation of the 1530 nm radiance measurement is key for a robust retrieval of particle size information. It is also found that using OSIRIS measurements at the different solar geometries available on the Odin orbit simultaneously provides little additional benefit. Based on these results, an improved aerosol retrieval algorithm is developed that couples the retrieval of aerosol extinction and mode radius of a log-normal particle size distribution. Comparison of these results with coincident measurements from SAGE III shows agreement in retrieved extinction to within approximately 10% over the bulk of the aerosol layer, which is comparable to version 5. The retrieved particle size, when converted to Ångström coefficient, shows good qualitative agreement with SAGE II measurements made at somewhat shorter wavelengths.

  2. The 2005 Study of Organic Aerosols at Riverside (SOAR-1): instrumental intercomparisons and fine particle composition

    OpenAIRE

    K. S. Docherty; A. C. Aiken; Huffman, J. A.; Ulbrich, I.M.; Decarlo, P. F.; D. Sueper; Worsnop, D. R.; Snyder, D. C.; Grover, B. D.; Eatough, D. J.; A. H. Goldstein; P. J. Ziemann; Jimenez, J. L.

    2011-01-01

    Multiple state-of-the-art instruments sampled ambient aerosol in Riverside, California during the 2005 Study of Organic Aerosols at Riverside (SOAR) to investigate sources and chemical composition of fine particles (PMf) in the inland region of Southern California. This paper briefly summarizes the spatial, meteorological and gas-phase conditions during SOAR-1 (15 July–15 August) and provides detailed intercomparisons of complementary measurements and average PM

  3. Surface tensions, viscosities, and diffusion constants in mixed component single aerosol particles

    Science.gov (United States)

    Bzdek, Bryan; Marshall, Frances; Song, Young-Chul; Haddrell, Allen; Reid, Jonathan

    2016-04-01

    Surface tension and viscosity are important aerosol properties but are challenging to measure on individual particles owing to their small size and mass. Aerosol viscosity impacts semivolatile partitioning from the aerosol phase, molecular diffusion in the bulk of the particle, and reaction kinetics. Aerosol surface tension impacts how particles activate to serve as cloud condensation nuclei. Knowledge of these properties and how they change under different conditions hinders accurate modelling of aerosol physical state and atmospheric impacts. We present measurements made using holographic optical tweezers to directly determine the viscosity and surface tension of optically trapped droplets containing ~1-4 picolitres of material (corresponding to radii of ~5-10 micrometres). Two droplets are captured in the experimental setup, equilibrated to a relative humidity, and coalesced through manipulation of the relative trap positions. The moment of coalescence is captured using camera imaging as well as from elastically backscattered light connected to an oscilloscope. For lower viscosity droplets, the relaxation in droplet shape to a sphere follows the form of a damped oscillator and gives the surface tension and viscosity. For high viscosity droplets, the relaxation results in a slow merging of the two droplets to form a sphere and the timescale of that process permits determination of viscosity. We show that droplet viscosity and surface tension can be quantitatively determined to within diffusion constants, vapour pressures, and reactive uptake coefficients for a mixed component aerosol undergoing oxidation and volatilisation will be discussed.

  4. Influence of crustal dust and sea spray supermicron particle concentrations and acidity on inorganic NO3- aerosol during the 2013 Southern Oxidant and Aerosol Study

    Energy Technology Data Exchange (ETDEWEB)

    Allen, Hannah M.; Draper, Danielle C.; Ayres, Benjamin R.; Ault, Andrew P.; Bondy, Amy L.; Takahama, S.; Modini, Robert; Baumann, K.; Edgerton, Eric S.; Knote, Christoph; Laskin, Alexander; Wang, Bingbing; Fry, Juliane L.

    2015-09-25

    The inorganic aerosol composition was measured in the southeastern United States, a region that exhibits high aerosol mass loading during the summer, as part of the 1 June to 15 July 2013 Southern Oxidant and Aerosol Study (SOAS) campaign. Measurements using a Monitor for AeRosols and GAses (MARGA), an ion chromatograph coupled with a wet rotating denuder and a steam-jet aerosol collector for monitoring of ambient inorganic gas and aerosol species, revealed two periods of high aerosol nitrate (NO3 ) concentrations during the campaign. These periods of high nitrate were correlated with increased concentrations of coarse mode mineral or sea spray aerosol species, particularly Na+ and Ca2+, and with a shift towards aerosol with larger (1 to 2.5 um) diameters. We suggest this nitrate aerosol forms by multiphase reactions of HNO3 and particles, reactions that are facilitated by transport of mineral dust and sea spray aerosol from a source within the United States. The observed high aerosol acidity prevents the formation of NH4NO3, the inorganic nitrogen species often dominant in fine-mode aerosol at higher pH. Calculation of the rate of the heterogeneous uptake of HNO3 on mineral aerosol supports the conclusion that aerosol NO3 is produced primarily by this process, and is likely limited by the availability of mineral dust surface area. Modeling of NO3 and HNO3 by thermodynamic equilibrium models (ISORROPIA II and E-AIM) reveals the importance of including mineral cations in the southeastern United States to accurately balance ion species and predict gas/aerosol phase partitioning.

  5. Effective Density and Mixing State of Aerosol Particles in a Near-Traffic Urban Environment

    DEFF Research Database (Denmark)

    Rissler, Jenny; Nordin, Erik Z; Eriksson, Axel C;

    2014-01-01

    In urban environments, airborne particles are continuously emitted, followed by atmospheric aging. Also, particles emitted elsewhere, transported by winds, contribute to the urban aerosol. We studied the effective density (mass-mobility relationship) and mixing state with respect to the density of...... particles in central Copenhagen, in wintertime. The results are related to particle origin, morphology, and aging. Using a differential mobility analyzer-aerosol particle mass analyzer (DMA-APM), we determined that particles in the diameter range of 50-400 nm were of two groups: porous soot aggregates and......-range transport from polluted continental areas. The effective density of each group was relatively stable over time, especially of the soot aggregates, which had effective densities similar to those observed in laboratory studies of fresh diesel exhaust emissions. When heated to 300 °C, the soot aggregate...

  6. Modelling Dry Deposition of Aerosol Particles onto Rough Surfaces

    Czech Academy of Sciences Publication Activity Database

    Tareq, H.; Smolík, Jiří; Kulmala, M.

    Helsinki : -, 2010, 11F6. ISBN N. [International Aerosol Conference IAC 2010. Helsinki (FI), 29.08.2010-03.09.2010] Institutional research plan: CEZ:AV0Z40720504 Keywords : parameterization * boundary layer * velocity profile Subject RIV: CF - Physical ; Theoretical Chemistry www.iac2010.fi

  7. Spontaneous Aerosol Ejection: Origin of Inorganic Particles in Biomass Pyrolysis.

    Science.gov (United States)

    Teixeira, Andrew R; Gantt, Rachel; Joseph, Kristeen E; Maduskar, Saurabh; Paulsen, Alex D; Krumm, Christoph; Zhu, Cheng; Dauenhauer, Paul J

    2016-06-01

    At high thermal flux and temperatures of approximately 500 °C, lignocellulosic biomass transforms to a reactive liquid intermediate before evaporating to condensable bio-oil for downstream upgrading to renewable fuels and chemicals. However, the existence of a fraction of nonvolatile compounds in condensed bio-oil diminishes the product quality and, in the case of inorganic materials, catalyzes undesirable aging reactions within bio-oil. In this study, ablative pyrolysis of crystalline cellulose was evaluated, with and without doped calcium, for the generation of inorganic-transporting aerosols by reactive boiling ejection from liquid intermediate cellulose. Aerosols were characterized by laser diffraction light scattering, inductively coupled plasma spectroscopy, and high-speed photography. Pyrolysis product fractionation revealed that approximately 3 % of the initial feed (both organic and inorganic) was transported to the gas phase as aerosols. Large bubble-to-aerosol size ratios and visualization of significant late-time ejections in the pyrolyzing cellulose suggest the formation of film bubbles in addition to the previously discovered jet formation mechanism. PMID:27125341

  8. Evaluation of the Particle Aerosolization from n-TiO2 Photocatalytic Nanocoatings under Abrasion

    OpenAIRE

    Neeraj Shandilya; Olivier Le Bihan; Christophe Bressot; Martin Morgeneyer

    2014-01-01

    A parametric study on the release of titanium dioxide (TiO2) nanoparticles from two commercial photocatalytic nanocoatings is carried out. For this, abrasion tests are performed on them. The formed aerosols are characterized by their number concentration, particle size distribution, individual particle shape, size, and chemical composition. The two nanocoatings appear to exhibit contrastingly opposite behavior with respect to the number concentration of the released particles. Having irregula...

  9. Quantification of environmentally persistent free radicals and reactive oxygen species in atmospheric aerosol particles

    OpenAIRE

    Arangio, Andrea M.; Tong, Haijie; Socorro, Joanna; Pöschl, Ulrich; Shiraiwa, Manabu

    2016-01-01

    Fine particulate matter plays a central role in adverse health effects of air pollution. Inhalation and deposition of aerosol particles in the respiratory tract can lead to the release of reactive oxygen species (ROS), which may cause oxidative stress. In this study, we have detected and quantified a wide range of particle-associated radicals using electron paramagnetic resonance (EPR) spectroscopy. Ambient particle samples were collected using a cascade impactor at a semi-urban site in centr...

  10. Carbonaceous composition changes of heavy-duty diesel engine particles in relation to biodiesels, aftertreatments and engine loads.

    Science.gov (United States)

    Cheng, Man-Ting; Chen, Hsun-Jung; Young, Li-Hao; Yang, Hsi-Hsien; Tsai, Ying I; Wang, Lin-Chi; Lu, Jau-Huai; Chen, Chung-Bang

    2015-10-30

    Three biodiesels and two aftertreatments were tested on a heavy-duty diesel engine under the US FTP transient cycle and additional four steady engine loads. The objective was to examine their effects on the gaseous and particulate emissions, with emphasis given to the organic and elemental carbon (OC and EC) in the total particulate matter. Negligible differences were observed between the low-sulfur (B1S50) and ultralow-sulfur (B1S10) biodiesels, whereas small reductions of OC were identified with the 10% biodiesel blend (B10). The use of diesel oxidation catalyst (DOC1) showed moderate reductions of EC and particularly OC, resulting in the OC/EC ratio well below unity. The use of DOC plus diesel particulate filter (DOC2+DPF) yielded substantial reductions of OC and particularly EC, resulting in the OC/EC ratio well above unity. The OC/EC ratios were substantially above unity at idle and low load, whereas below unity at medium and high load. The above changes in particulate OC and EC are discussed with respect to the fuel content, pollutant removal mechanisms and engine combustion conditions. Overall, the present study shows that the carbonaceous composition of PM could change drastically with engine load and aftertreatments, and to a lesser extent with the biodiesels under study. PMID:25974660

  11. MAPPIX: A software package for off-line micro-pixe single particle aerosol analysis

    International Nuclear Information System (INIS)

    In the framework of a multiannual experiment performed at Baia Terra Nova, Antarctica, size-segregated aerosol samples were collected by using a 12-stage SDI impactor (Hillamo design). Approximately 2800 particles, belonging to the first four supermicrometric SDI stages - 8.39, 4.08, 2.68, 1.66 μm dynamic aerosol diameter cuts - were analyzed at the INFN-LNL micro-PIXE facility, a three lens Oxford Microprobe (OM) product, installed in the early nineties. Four regions on each of the 12 sub-samples were measured; 60 aerosol particles were detected on average in each of the analyzed regions. The off-line single aerosol particle (SAP) analysis of such big amount of data required software that is able to rapidly handle the acquired data, with a simple and fast area selection procedure; the subsequent automated PIXE spectra analysis with a specialized code was also needed. The MAPPIX 2.0 software was designed to make easier and faster the user jobs during the SAP analysis. The package is composed of two separate routines: the first one is devoted to data format conversion (OM-LMF file format to MAPPIX format), while the second one is devoted to micro-PIXE maps graphical presentation and aerosol particle selection procedure. The MAPPIX data format and software features will be discussed; a short report of the speed performances will be presented.

  12. MAPPIX: A software package for off-line micro-pixe single particle aerosol analysis

    Science.gov (United States)

    Ceccato, D.

    2009-06-01

    In the framework of a multiannual experiment performed at Baia Terra Nova, Antarctica, size-segregated aerosol samples were collected by using a 12-stage SDI impactor (Hillamo design). Approximately 2800 particles, belonging to the first four supermicrometric SDI stages - 8.39, 4.08, 2.68, 1.66 μm dynamic aerosol diameter cuts - were analyzed at the INFN-LNL micro-PIXE facility, a three lens Oxford Microprobe (OM) product, installed in the early nineties. Four regions on each of the 12 sub-samples were measured; 60 aerosol particles were detected on average in each of the analyzed regions. The off-line single aerosol particle (SAP) analysis of such big amount of data required software that is able to rapidly handle the acquired data, with a simple and fast area selection procedure; the subsequent automated PIXE spectra analysis with a specialized code was also needed. The MAPPIX 2.0 software was designed to make easier and faster the user jobs during the SAP analysis. The package is composed of two separate routines: the first one is devoted to data format conversion (OM-LMF file format to MAPPIX format), while the second one is devoted to micro-PIXE maps graphical presentation and aerosol particle selection procedure. The MAPPIX data format and software features will be discussed; a short report of the speed performances will be presented.

  13. Aerosol and Cloud-Nucleating Particle Observations during an Atmospheric River Event

    Science.gov (United States)

    DeMott, P. J.; McCluskey, C. S.; Petters, M.; Suski, K. J.; Levin, E. J.; Hill, T. C. J.; Atwood, S. A.; Schill, G. P.; Rocci, K.; Boose, Y.; Martin, A.; Cornwell, G.; Al-Mashat, H.; Moore, K.; Prather, K. A.; Rothfuss, N.; Taylor, H.; Leung, L. R.; Tomlinson, J. M.; Mei, F.; Hubbe, J. M.; Rosenfeld, D.; Spackman, J. R.; Fairall, C. W.; Creamean, J.; White, A. B.; Kreidenweis, S. M.

    2015-12-01

    The multi-agency CalWater 2015 project occurred over North Central CA and the Eastern Pacific during January to March 2015 (Spackman et al., this session). The goals of the campaign were to document the structure of atmospheric rivers (ARs) that deliver much of the water vapor associated with major winter storms along the U.S. West Coast and to investigate the modulating effect of aerosols on precipitation. Aerosol sources that may influence orographic cloud properties for air lifted over the mountains in California in winter include pollution, biomass burning, soil dusts and marine aerosols, but their roles will also be influenced by transport, vertical stratification, and scavenging processes. We present results from a comprehensive study of aerosol distributions, compositions, and cloud nucleating properties during an intense winter storm during February 2015, including data from an NSF-supported measurement site at Bodega Bay, from the DOE-ARM Cloud Aerosol Precipitation Experiment that included sampling on the NOAA RV Ron Brown offshore and the G-1 aircraft over ocean and land, and with context provided by other NOAA aircraft and remote sensing facilities. With a special focus on the coastal site, we discuss changes in aerosol distributions, aerosol hygroscopicity, and number concentrations of fluorescent particles, cloud condensation nuclei (CCN), and ice nucleating particles (INPs) during the AR event. We compare with periods preceding and following the event. For example, total aerosol number and surface area concentrations at below 0.5 μm diameter decreased from typical values of a few thousand cm-3 and 100 μm2 cm-3, respectively, to a few hundred cm-3 and 10 μm2cm-3 at Bodega Bay during the AR event. CCN concentrations were similarly lower, but hygroscopicity parameter (kappa) increased from typical values of 0.2 to values > 0.5 during the AR.INP and fluorescent particle number concentrations were generally lower during the AR event than at any other

  14. Development and experimental evaluation of an optical sensor for aerosol particle characterization

    Energy Technology Data Exchange (ETDEWEB)

    Somesfalean, G.

    1998-03-01

    A sensor for individual aerosol particle characterization, based on a single-mode semiconductor laser coupled to an external cavity is presented. The light emitting semiconductor laser acts as a sensitive optical detector itself, and the whole system has the advantage of using conventional optical components and providing a compact set-up. Aerosol particles moving through the sensing volume, which is located in the external cavity of a semiconductor laser, scatter and absorb light. Thereby they act as small disturbances on the electromagnetic field inside the dynamic multi-cavity laser system. From the temporal variation of the output light intensity, information about the number, velocity, size, and refractive index of the aerosol particles can be derived. The diffracted light in the near-forward scattering direction is collected and Fourier-transformed by a lens, and subsequently imaged on a CCD camera. The recorded Fraunhofer diffraction pattern provides information about the projected area of the scattering particle, and can thus be used to determine the size and the shape of aerosol particles. The sensor has been tested on fibers which are of interest in the field of working environment monitoring. The recorded output intensity variation has been analysed, and the relationship between the shape and the size of each fibre, and the resulting scattering profiles has been investigated. A simple one-dimensional model for the optical feedback variation due to the light-particle interaction in the external cavity is also discussed 34 refs, 26 figs, 6 tabs

  15. Research on the optical properties for randomly oriented aerosol aggregation particles

    International Nuclear Information System (INIS)

    Cluster-cluster aggregation (CCA) model is used to simulate four kinds of randomly oriented aerosol aggregation particles consisting of 64 spherical original particles. Combined with the discrete dipole approximation method, the numerical results of asymmetry parameter, absorption, scattering and extinction efficiency factors under different incident angles and different size parameters are gotten respectively, and the differences of asymmetry parameter, absorption, scattering and extinction efficiency factors among the four shapes of aerosol aggregation particles are compared and analyzed. The results show that their optical properties are significantly dependent on the incident angle and shapes for the aerosol aggregation particles with same number of original particles. And for the aerosol aggregation particles with different size parameters, when the wavelength of incident light is given, initially, the absorption, scattering and extinction efficiency factors increase rapidly with the increasing size parameter, and then slowly become smaller, so there is a maximum value for these factors in the process of changes in the size parameter. The asymmetry factor increases with the increase of the size parameter and tends to 1. (authors)

  16. Aerosol number size distributions over a coastal semi urban location: Seasonal changes and ultrafine particle bursts.

    Science.gov (United States)

    Babu, S Suresh; Kompalli, Sobhan Kumar; Moorthy, K Krishna

    2016-09-01

    Number-size distribution is one of the important microphysical properties of atmospheric aerosols that influence aerosol life cycle, aerosol-radiation interaction as well as aerosol-cloud interactions. Making use of one-yearlong measurements of aerosol particle number-size distributions (PNSD) over a broad size spectrum (~15-15,000nm) from a tropical coastal semi-urban location-Trivandrum (Thiruvananthapuram), the size characteristics, their seasonality and response to mesoscale and synoptic scale meteorology are examined. While the accumulation mode contributed mostly to the annual mean concentration, ultrafine particles (having diameter <100nm) contributed as much as 45% to the total concentration, and thus constitute a strong reservoir, that would add to the larger particles through size transformation. The size distributions were, in general, bimodal with well-defined modes in the accumulation and coarse regimes, with mode diameters lying in the range 141 to 167nm and 1150 to 1760nm respectively, in different seasons. Despite the contribution of the coarse sized particles to the total number concentration being meager, they contributed significantly to the surface area and volume, especially during transport of marine air mass highlighting the role of synoptic air mass changes. Significant diurnal variation occurred in the number concentrations, geometric mean diameters, which is mostly attributed to the dynamics of the local coastal atmospheric boundary layer and the effect of mesoscale land/sea breeze circulation. Bursts of ultrafine particles (UFP) occurred quite frequently, apparently during periods of land-sea breeze transitions, caused by the strong mixing of precursor-rich urban air mass with the cleaner marine air mass; the resulting turbulence along with boundary layer dynamics aiding the nucleation. These ex-situ particles were observed at the surface due to the transport associated with boundary layer dynamics. The particle growth rates from

  17. Quantification of bitumen particles in aerosol and soil samples using HP-GPC

    DEFF Research Database (Denmark)

    Fauser, Patrik; Tjell, Jens Christian; Mosbæk, Hans;

    2000-01-01

    A method for identifying and quantifying bitumen particles, generated from the wear of roadway asphalts, in aerosol and soil samples has been developed. Bitumen is found to be the only contributor to airborne particles containing organic molecules with molecular weights larger than 2000 g pr. mol....... These are separated and identified using High Performance Gel Permeation Chromatography (HP-GPC) with fluorescence detection. As an additional detection method Infra Red spectrometry (IR) is employed for selected samples. The methods have been used on aerosol, soil and other samples....

  18. Measurement of overall uptake coefficients for HO2 radicals by aerosol particles sampled from ambient air at Mts. Tai and Mang (China)

    OpenAIRE

    Taketani, F.; Y. Kanaya; P. Pochanart; Liu, Y; Li, J.; K. Okuzawa; K. Kawamura; Z. Wang; H. Akimoto

    2012-01-01

    HO2 uptake coefficients for ambient aerosol particles, collected on quartz fiber filter using a high-volume air sampler in China, were measured using an aerosol flow tube coupled with a chemical conversion/laser-induced fluorescence technique at 760 Torr and 298 K, with a relative humidity of 75%. Aerosol particles were regenerated with an atomizer using the water extracts from the aerosol particles. Over 10 samples, the measured HO2 uptake coefficients for the aerosol parti...

  19. Ice cloud processing of ultra-viscous/glassy aerosol particles leads to enhanced ice nucleation ability

    Directory of Open Access Journals (Sweden)

    B. J. Murray

    2012-04-01

    Full Text Available The ice nucleation potential of airborne glassy aqueous aerosol particles has been investigated by controlled expansion cooling cycles in the AIDA aerosol and cloud chamber of the Karlsruhe Institute of Technology at temperatures between 247 and 216 K. Four different solutes were used as proxies for oxygenated organic matter found in the atmosphere: raffinose, 4-hydroxy-3-methoxy-DL-mandelic acid (HMMA, levoglucosan, and a multi-component mixture of raffinose with five dicarboxylic acids and ammonium sulphate. Similar to previous experiments with citric acid aerosols, all particles were found to nucleate ice heterogeneously before reaching the homogeneous freezing threshold provided that the freezing cycles were started well below the respective glass transition temperatures of the compounds; this is discussed in detail in a separate article. In this contribution, we identify a further mechanism by which glassy aerosols can promote ice nucleation below the homogeneous freezing limit. If the glassy aerosol particles are probed in freezing cycles started only a few degrees below their respective glass transition temperatures, they enter the liquid regime of the state diagram upon increasing relative humidity (moisture-induced glass-to-liquid transition before being able to act as heterogeneous ice nuclei. Ice formation then only occurs by homogeneous freezing at elevated supersaturation levels. When ice forms the remaining solution freeze concentrates and re-vitrifies. If these ice cloud processed glassy aerosol particles are then probed in a second freezing cycle at the same temperature, they catalyse ice formation at a supersaturation threshold between 5 and 30% with respect to ice. By analogy with the enhanced ice nucleation ability of insoluble ice nuclei like mineral dusts after they nucleate ice once, we refer to this phenomenon as pre-activation. We propose a number of possible explanations for why glassy aerosols that have re-vitrified in

  20. Fluorescence from atmospheric aerosol detected by a lidar indicates biogenic particles in the stratosphere

    Directory of Open Access Journals (Sweden)

    F. Immler

    2004-09-01

    Full Text Available With a lidar system that was installed in Lindenberg/Germany, we observed in June 2003, an extended aerosol layer at 13 km altitude in the lowermost stratosphere. This layer created an inelastic backscatter signal which we interpret as laser induced fluorescence from aerosol particles. Also, we find evidence for inelastic scattering in a smoke plume from a forest fire that we observed in the troposphere. Fluorescence from ambient aerosol had not yet been considered detectable by lidar. However, organic compounds such as polycyclic aromatic hydrocarbons sticking to the aerosol particles, or bioaerosol such as bacteria, spores or pollen fluoresce when excited with UV-radiation in a way that is detectable by our lidar system. Therefore, we conclude that fluorescence from organic material released by biomass burning creates the inelastic backscatter signal that we measured with our instrument and thus demonstrate a new and powerful way to characterize aerosols by a remote sensing technique. The stratospheric aerosol layer that we have observed in Lindenberg for three consecutive days is likely to be a remnant from Siberian forest fire plumes lifted across the tropopause and transported around the globe.

  1. Development and characterization of a single particle laser ablation mass spectrometer (SPLAM for organic aerosol studies

    Directory of Open Access Journals (Sweden)

    F. Gaie-Levrel

    2011-07-01

    Full Text Available A single particle instrument has been developed for real-time analysis of organic aerosols. This instrument, named Single Particle Laser Ablation Mass Spectrometry (SPLAM, samples particles using an aerodynamic lens system for which the theoretical performances were calculated. At the outlet of this system, particle detection and sizing are realized using two continuous diode lasers operating at λ = 403 nm. Polystyrene Latex (PSL, sodium chloride (NaCl and dioctylphtalate (DOP particles were used to characterize and calibrate optical detection of SPLAM. The optical detection limit (DL and detection efficiency (DE were determined using size-selected DOP particles. The DE is ranging from 0.1 to 90 % for 100 and 350 nm DOP particles respectively and the SPLAM instrument is able to detect and size-resolve particles as small as 110–120 nm. Scattered light is detected by two photomultipliers and the detected signals are used to trigger a UV excimer laser (λ = 248 nm used for laser desorption ionization (LDI of individual aerosol particles. The formed ions are analyzed by a 1 m linear time-of-flight mass spectrometer in order to access to the chemical composition of individual particles. The TOF-MS detection limit for gaseous aromatic compounds was determined to be 0.85 attograms. DOP particles were also used to test the overall functioning of the instrument. The analysis of a secondary organic aerosol, formed in a smog chamber by the ozonolysis of indene, is presented as a first scientific application of the instrument. Single particle mass spectra are obtained with a global hit rate of 10 %. They are found to be very different from one particle to another, reflecting chemical differences of the analyzed particles, and most of the detected mass peaks are attributed to oxidized products of indene.

  2. Carbonaceous composition changes of heavy-duty diesel engine particles in relation to biodiesels, aftertreatments and engine loads

    Energy Technology Data Exchange (ETDEWEB)

    Cheng, Man-Ting; Chen, Hsun-Jung [Department of Environmental Engineering, National Chung Hsing University, 250 Kuo-Kuang Road, Taichung 40254, Taiwan (China); Young, Li-Hao, E-mail: lhy@mail.cmu.edu.tw [Department of Occupational Safety and Health, China Medical University, 91 Hsueh-Shih Road, Taichung 40402, Taiwan (China); Yang, Hsi-Hsien [Department of Environmental Engineering and Management, Chaoyang University of Technology, 168, Jifeng E. Road, Wufeng District, Taichung 41349, Taiwan (China); Tsai, Ying I. [Department of Environmental Engineering and Science, Chia Nan University of Pharmacy and Science, 60, Sec. 1, Erren Rd., Rende District, Tainan 71710, Taiwan (China); Wang, Lin-Chi [Department of Civil Engineering and Geomatics, Cheng Shiu University, 840, Chengcing Road, Niaosong District, Kaohsiung 83347, Taiwan (China); Lu, Jau-Huai [Department of Mechanical Engineering, National Chung Hsing University, 250 Kuo-Kuang Road, Taichung 40254, Taiwan (China); Chen, Chung-Bang [Fuel Quality and Engine Performance Research, Refining and Manufacturing Research Institute, Chinese Petroleum Corporation, 217, Minsheng S. Road, West District, Chiayi 60051, Taiwan (China)

    2015-10-30

    Highlights: • We study particulate OC and EC under 3 fuels, 2 aftertreatments and 4 engine loads. • Negligible to minor OC and EC changes with low, ultralow sulfur and 10% biodiesels. • Moderate reductions of EC and particularly OC from diesel oxidation catalyst (DOC). • Large reductions of OC and particularly EC from DOC plus diesel particulate filter. • Highest at idle, whereas OC decreases but EC increases from low to high load. - Abstract: Three biodiesels and two aftertreatments were tested on a heavy-duty diesel engine under the US FTP transient cycle and additional four steady engine loads. The objective was to examine their effects on the gaseous and particulate emissions, with emphasis given to the organic and elemental carbon (OC and EC) in the total particulate matter. Negligible differences were observed between the low-sulfur (B1S50) and ultralow-sulfur (B1S10) biodiesels, whereas small reductions of OC were identified with the 10% biodiesel blend (B10). The use of diesel oxidation catalyst (DOC1) showed moderate reductions of EC and particularly OC, resulting in the OC/EC ratio well below unity. The use of DOC plus diesel particulate filter (DOC2+DPF) yielded substantial reductions of OC and particularly EC, resulting in the OC/EC ratio well above unity. The OC/EC ratios were substantially above unity at idle and low load, whereas below unity at medium and high load. The above changes in particulate OC and EC are discussed with respect to the fuel content, pollutant removal mechanisms and engine combustion conditions. Overall, the present study shows that the carbonaceous composition of PM could change drastically with engine load and aftertreatments, and to a lesser extent with the biodiesels under study.

  3. Carbonaceous composition changes of heavy-duty diesel engine particles in relation to biodiesels, aftertreatments and engine loads

    International Nuclear Information System (INIS)

    Highlights: • We study particulate OC and EC under 3 fuels, 2 aftertreatments and 4 engine loads. • Negligible to minor OC and EC changes with low, ultralow sulfur and 10% biodiesels. • Moderate reductions of EC and particularly OC from diesel oxidation catalyst (DOC). • Large reductions of OC and particularly EC from DOC plus diesel particulate filter. • Highest at idle, whereas OC decreases but EC increases from low to high load. - Abstract: Three biodiesels and two aftertreatments were tested on a heavy-duty diesel engine under the US FTP transient cycle and additional four steady engine loads. The objective was to examine their effects on the gaseous and particulate emissions, with emphasis given to the organic and elemental carbon (OC and EC) in the total particulate matter. Negligible differences were observed between the low-sulfur (B1S50) and ultralow-sulfur (B1S10) biodiesels, whereas small reductions of OC were identified with the 10% biodiesel blend (B10). The use of diesel oxidation catalyst (DOC1) showed moderate reductions of EC and particularly OC, resulting in the OC/EC ratio well below unity. The use of DOC plus diesel particulate filter (DOC2+DPF) yielded substantial reductions of OC and particularly EC, resulting in the OC/EC ratio well above unity. The OC/EC ratios were substantially above unity at idle and low load, whereas below unity at medium and high load. The above changes in particulate OC and EC are discussed with respect to the fuel content, pollutant removal mechanisms and engine combustion conditions. Overall, the present study shows that the carbonaceous composition of PM could change drastically with engine load and aftertreatments, and to a lesser extent with the biodiesels under study

  4. Characterizing the impact of urban emissions on regional aerosol particles: airborne measurements during the MEGAPOLI experiment

    Science.gov (United States)

    Freney, E. J.; Sellegri, K.; Canonaco, F.; Colomb, A.; Borbon, A.; Michoud, V.; Doussin, J.-F.; Crumeyrolle, S.; Amarouche, N.; Pichon, J.-M.; Bourianne, T.; Gomes, L.; Prevot, A. S. H.; Beekmann, M.; Schwarzenböeck, A.

    2014-02-01

    The MEGAPOLI (Megacities: Emissions, urban, regional and Global Atmospheric POLlution and climate effects, and Integrated tools for assessment and mitigation) experiment took place in July 2009. The aim of this campaign was to study the aging and reactions of aerosol and gas-phase emissions in the city of Paris. Three ground-based measurement sites and several mobile platforms including instrument equipped vehicles and the ATR-42 aircraft were involved. We present here the variations in particle- and gas-phase species over the city of Paris, using a combination of high-time resolution measurements aboard the ATR-42 aircraft. Particle chemical composition was measured using a compact time-of-flight aerosol mass spectrometer (C-ToF-AMS), giving detailed information on the non-refractory submicron aerosol species. The mass concentration of black carbon (BC), measured by a particle absorption soot photometer (PSAP), was used as a marker to identify the urban pollution plume boundaries. Aerosol mass concentrations and composition were affected by air-mass history, with air masses that spent longest time over land having highest fractions of organic aerosol and higher total mass concentrations. The Paris plume is mainly composed of organic aerosol (OA), BC, and nitrate aerosol, as well as high concentrations of anthropogenic gas-phase species such as toluene, benzene, and NOx. Using BC and CO as tracers for air-mass dilution, we observe the ratio of ΔOA / ΔBC and ΔOA / ΔCO increase with increasing photochemical age (-log(NOx / NOy)). Plotting the equivalent ratios of different organic aerosol species (LV-OOA, SV-OOA, and HOA) illustrate that the increase in OA is a result of secondary organic aerosol (SOA) formation. Within Paris the changes in the ΔOA / ΔCO are similar to those observed during other studies in London, Mexico City, and in New England, USA. Using the measured SOA volatile organic compounds (VOCs) species together with organic aerosol formation

  5. Size Dependence of Chemical Reactions in Nanoscale Aerosol Particles

    Czech Academy of Sciences Publication Activity Database

    Levdansky, V.V.; Smolík, Jiří; Moravec, Pavel

    Helsinki : -, 2010, P2L1. ISBN N. [International Aerosol Conference IAC 2010. Helsinki (FI), 29.08.2010-03.09.2010] R&D Projects: GA ČR GA104/07/1093; GA ČR GA101/09/1633; GA AV ČR(CZ) IAA400720804 Institutional research plan: CEZ:AV0Z40720504 Keywords : size effect * nanoparticles * chemical reactions Subject RIV: CF - Physical ; Theoretical Chemistry www.iac2010.fi

  6. A novel tandem differential mobility analyzer with organic vapor treatment of aerosol particles

    Directory of Open Access Journals (Sweden)

    J. Joutsensaari

    2001-01-01

    Full Text Available A novel method to characterize the organic composition of aerosol particles has been developed. The method is based on organic vapor interaction with aerosol particles and it has been named an Organic Tandem Differential Mobility Analyzer (OTDMA. The OTDMA method has been tested for inorganic (sodium chloride and ammonium sulfate and organic (citric acid and adipic acid particles. Growth curves of the particles have been measured in ethanol vapor and as a comparison in water vapor as a function of saturation ratio. Measurements in water vapor show that sodium chloride and ammonium sulfate as well as citric acid particles grow at water saturation ratios (S of 0.8 and above, whereas adipic acid particles do not grow at S S = 0.75 and S = 0.79, respectively. Citric acid particles grow monotonously with increasing saturation ratios already at low saturation ratios and no clear deliquescence point is found. For sodium chloride and ammonium sulfate particles, no growth can be seen in ethanol vapor at saturation ratios below 0.93. In contrast, for adipic acid particles, the deliquescence takes place at around S = 0.95 in the ethanol vapor. The recrystallization of adipic acid takes place at S The results show that the working principles of the OTDMA are operational for single-component aerosols. Furthermore, the results indicate that the OTDMA method may prove useful in determining whether aerosol particles contain organic substances, especially if the OTDMA is operated in parallel with a hygroscopicity TDMA, as the growth of many substances is different in ethanol and water vapors.

  7. Polarization properties of aerosol particles over western Japan: classification, seasonal variation, and implications for air quality

    Science.gov (United States)

    Pan, Xiaole; Uno, Itsushi; Hara, Yukari; Osada, Kazuo; Yamamoto, Shigekazu; Wang, Zhe; Sugimoto, Nobuo; Kobayashi, Hiroshi; Wang, Zifa

    2016-08-01

    Ground-based observation of the polarization properties of aerosol particles using a polarization optical particle counter (POPC) was made from 27 October 2013, to 31 December 2015, at a suburban site in the Kyushu area of Japan. We found that the depolarization ratio (DR, the fraction of s-polarized signal in the total backward light scattering signal) of aerosol particles showed prominent seasonal variability, with peaks in spring (0.21-0.23) and winter (0.19-0.23), and a minimum value (0.09-0.14) in summer. The aerosol compositions in both fine mode (aerodynamic diameter of particle, Dp particles, sea salt, and anthropogenic pollution-dominant aerosols. The DR value increased with increasing particle size, and DR = 0.1 was a reliable threshold value to identify the sphericity of supermicron (Dp > 1 µm) particles. Occurrence of substandard air quality days in Kyushu was closely related with mixed type (coexistence of anthropogenic pollutants and dust particles in the atmosphere), especially in winter and spring, indicating that dust events in the Asian continent played a key role in the cross-boundary transport of continental pollution. Backward trajectory analysis demonstrated that air masses originating from the western Pacific contained large amounts of spherical particles due to the influence of sea salt, especially in summer; however, for air masses from the Asian continent, the dependence of number fraction of spherical particles on air relative humidity was insignificant, indicating the predominance of less-hygroscopic substances (e.g., mineral dust), although the mass concentrations of anthropogenic pollutants were elevated.

  8. Effect of particle settling on lidar profiles of long-range transported Saharan aerosols

    Science.gov (United States)

    Gasteiger, Josef; Groß, Silke

    2016-04-01

    A large amount of desert aerosol is transported in the Saharan Air Layer (SAL) westwards from Africa over the Atlantic Ocean. Lidar profiles of transported Saharan aerosol may contain some information about the vertically-resolved aerosol microphysics that could be used to characterize processes that affected the measured aerosol during transport. We present modelled lidar profiles of long-range transported Saharan aerosol assuming that initially the SAL is well-mixed and that there is no vertical mixing of air within the SAL as soon as it reaches the Atlantic. We consider Stokes gravitational settling of aerosol particles over the ocean. The lidar profiles are calculated using optical models for irregularly-shaped mineral dust particles assuming settling-induced particle removal as function of distance from the SAL top. Within the SAL we find a decrease of both the backscatter coefficients and the linear depolarization ratios with decreasing distance from the SAL top. For example, the linear depolarization ratio at a wavelength of 532nm decreases from 0.289 at 1000m to 0.256 at 200m and 0.215 at 100m below SAL top. We compare the modelled backscatter coefficients and linear depolarization ratios to ground-based lidar measurements performed during the SALTRACE field campaign in Barbados (Caribbean) and find agreement within the estimated uncertainties. We discuss the uncertainties of our modeling approach in our presentation. Assumed mineral dust particle shapes, assumed particle mixture properties, and assumptions about processes in the SAL over the continent and the ocean are important aspects to be considered. Uncertainties are relevant for the potential of lidar measurements of transported Saharan dust to learn something about processes occuring in the SAL during long-range transport. We also compare our modeling results to modeling results previously published in the literature.

  9. Water uptake of clay and desert dust aerosol particles at sub- and supersaturated water vapor conditions.

    Science.gov (United States)

    Herich, Hanna; Tritscher, Torsten; Wiacek, Aldona; Gysel, Martin; Weingartner, Ernest; Lohmann, Ulrike; Baltensperger, Urs; Cziczo, Daniel J

    2009-09-28

    Airborne mineral dust particles serve as cloud condensation nuclei (CCN), thereby influencing the formation and properties of warm clouds. It is therefore of atmospheric interest how dust aerosols with different mineralogy behave when exposed to high relative humidity (RH) or supersaturation (SS) with respect to liquid water. In this study the subsaturated hygroscopic growth and the supersaturated cloud condensation nucleus activity of pure clays and real desert dust aerosols were determined using a hygroscopicity tandem differential mobility analyzer (HTDMA) and a cloud condensation nuclei counter (CCNC), respectively. Five different illite, montmorillonite and kaolinite clay samples as well as three desert dust samples (Saharan dust (SD), Chinese dust (CD) and Arizona test dust (ATD)) were investigated. Aerosols were generated both with a wet and a dry disperser. The water uptake was parameterized via the hygroscopicity parameter kappa. The hygroscopicity of dry generated dust aerosols was found to be negligible when compared to processed atmospheric aerosols, with CCNC derived kappa values between 0.00 and 0.02 (the latter corresponds to a particle consisting of 96.7% by volume insoluble material and approximately 3.3% ammonium sulfate). Pure clay aerosols were generally found to be less hygroscopic than natural desert dust particles. The illite and montmorillonite samples had kappa approximately 0.003. The kaolinite samples were less hygroscopic and had kappa=0.001. SD (kappa=0.023) was found to be the most hygroscopic dry-generated desert dust followed by CD (kappa=0.007) and ATD (kappa=0.003). Wet-generated dust showed an increased water uptake when compared to dry-generated samples. This is considered to be an artifact introduced by redistribution of soluble material between the particles. Thus, the generation method is critically important when presenting such data. These results indicate any atmospheric processing of a fresh mineral dust particle which

  10. An aerosol dynamics model for simulating particle formation and growth in a mixed flow chamber

    Directory of Open Access Journals (Sweden)

    M. Vesterinen

    2011-02-01

    Full Text Available In this work we model the aerosol size distribution dynamics in a mixed flow chamber in which new particles are formed via nucleation and subsequent condensation of oxidation products of VOCs emitted from Norway spruce seedlings. The microphysical processes included in the model are nucleation, condensation, deposition and coagulation. The aerosol dynamics in the chamber is a competition between aerosol growth and scavenging/deposition which results in a cyclic particle formation process. With a simple 1-product model, in which the formed gas is able to both condense to the particles and nucleate, we are able to catch both the oscillatory features of the particle formation process and the evolution of the number concentration in a reasonable way. The gas-phase chemistry was adjusted using pre-estimated reaction rate constant in the simulations and the particle deposition rate as a function of size was determined experimentally. Despite this, some of the essential features of the physical properties of the aerosol population could still be captured and investigated without the detailed knowledge of the physical processes underlying the problem by using the constructed model. The size dependency of the wall loss coefficient was investigated using a slightly modified measurement set-up.

  11. Ultrasensitive detection of inhaled organic aerosol particles by accelerator mass spectrometry.

    Science.gov (United States)

    Parkhomchuk, E V; Gulevich, D G; Taratayko, A I; Baklanov, A M; Selivanova, A V; Trubitsyna, T A; Voronova, I V; Kalinkin, P N; Okunev, A G; Rastigeev, S A; Reznikov, V A; Semeykina, V S; Sashkina, K A; Parkhomchuk, V V

    2016-09-01

    Accelerator mass spectrometry (AMS) was shown to be applicable for studying the penetration of organic aerosols, inhaled by laboratory mice at ultra-low concentration ca. 10(3) cm(-3). We synthesized polystyrene (PS) beads, composed of radiocarbon-labeled styrene, for testing them as model organic aerosols. As a source of radiocarbon we used methyl alcohol with radioactivity. Radiolabeled polystyrene beads were obtained by emulsifier-free emulsion polymerization of synthesized (14)C-styrene initiated by K2S2O8 in aqueous media. Aerosol particles were produced by pneumatic spraying of diluted (14)C-PS latex. Mice inhaled (14)C-PS aerosol consisting of the mix of 10(3) 225-nm particles per 1 cm(3) and 5·10(3) 25-nm particles per 1 cm(3) for 30 min every day during five days. Several millions of 225-nm particles deposited in the lungs and slowly excreted from them during two weeks of postexposure. Penetration of particles matter was also observed for liver, kidneys and brain, but not for a heart. PMID:27281540

  12. Heterogeneous Ice Nucleation on Kaolinite Particles, Particle Surrogates of HUmic-Like Substances (HULIS), and Organics-Containing Urban Aerosols

    Science.gov (United States)

    Wang, B.; Knopf, D. A.

    2009-12-01

    Aerosol particles can affect the global radiation budget through aerosol-cloud interactions by acting as cloud condensation nuclei and ice nuclei (IN) thereby inducing new clouds and/or modifying the radiative properties of existing clouds. This study presents heterogeneous ice nucleation data as a function of particle temperature and relative humidity with respect to ice (RHice) for laboratory generated kaolinite particles, leonardite and fulvic acid particles serving as surrogates for aerosols composed of HULIS, and organics-containing urban aerosols collected during the MILAGRO (Mexico City) campaign. These experiments are conducted using an improved version of a previously developed ice nucleation cell coupled to an optical microscope which allows to control particle temperatures between 200-300 K and corresponding atmospherically relevant RHice. Micrometer-sized particles are deposited onto a hydrophobic substrate and are placed in the nucleation cell. To validate the experimental approach and quality of substrates, ice nucleation experiments were performed 1. on plain sample substrates and 2. using a well studied IN: kaolinite particles. The results corroborate that kaolinite particles are efficient IN inducing ice nucleation at 102-120% RHice via deposition mode at temperatures between 200 and 245 K, in agreement with previous studies. The ice nucleation efficiency of leonardite and fulvic acid particles with median diameters of 2-3 µm is determined. Leonardite particles nucleate ice via deposition mode at 120-140% RHice for temperatures between 200 and 240 K with the minimum RHice threshold observed at 220 K. Fulvic acid particles nucleate ice via deposition mode at 135-150% RHice for temperatures between 200 and 230 K with the minimum RHice threshold determined at 216 K. The fulvic acid particles take up water at RH>95% for temperatures between 235 and 250 K. The contact angle derived from experimentally determined heterogeneous ice nucleation rate

  13. Contribution to the study of nuclear aerosol: looking for the dynamic form factor of the aerosol of primary particles of sodium oxide

    International Nuclear Information System (INIS)

    The dynamical form factor describes the entrainment of any non spherical particle, of inhomogeneous density, in relation to the entrainment of a spherical particle with the same volume and some sedimentation speed. Experimental study of the form factor and particle size distribution of sodium peroxide primary aerosols

  14. Morphology of mixed primary and secondary organic particles and the adsorption of spectator organic gases during aerosol formation

    OpenAIRE

    Vaden, Timothy D.; Song, Chen; Zaveri, Rahul A.; Imre, Dan; Zelenyuk, Alla

    2010-01-01

    Primary organic aerosol (POA) and associated vapors can play an important role in determining the formation and properties of secondary organic aerosol (SOA). If SOA and POA are miscible, POA will significantly enhance SOA formation and some POA vapor will incorporate into SOA particles. When the two are not miscible, condensation of SOA on POA particles forms particles with complex morphology. In addition, POA vapor can adsorb to the surface of SOA particles increasing their mass and affecti...

  15. Production, Organic Characterization, and Phase Transformations of Marine Particles Aerosolized from a Laboratory Mesocosm Phytoplankton Bioreactor

    Science.gov (United States)

    Alpert, P. A.; Knopf, D. A.; Aller, J. Y.; Radway, J.; Kilthau, W.

    2012-12-01

    Previous studies have shown that particles emitted from bubble bursting and wave breaking of ocean waters with high biological activity can contain sea salts associated with organic material, with smaller particles containing a larger mass fraction of organics than larger particles. This likely indicates a link between phytoplankton productivity in oceans and particulate organic material in marine air. Once aerosolized, particles with significant amount of organic material can affect cloud activation and formation of ice crystals, among other atmospheric processes, thus influencing climate. This is significant for clouds and climate particularly over nutrient rich polar seas, in which concentrations of biological organisms can reach up to 109 cells per ml during spring phytoplankton blooms. Here we present results of bubble bursting aerosol production from a seawater mesocosm containing artificial seawater, natural seawater and unialgal cultures of three representative phytoplankton species. These phytoplankton (Thalassiosira pseudonana, Emilianaia huxleyi, and Nannochloris atomus), possessed siliceous frustules, calcareous frustules and no frustules, respectively. Bubbles were generated employing recirculating impinging water jets or glass frits. Dry and humidified aerosol size distributions and bulk aerosol organic composition were measured as a function of phytoplankton growth, and chlorophyll composition and particulate and dissolved organic carbon in the water were determined. Finally, particles were collected on substrates for ice nucleation and water uptake experiments, their elemental compositions were determined using computer controlled scanning electron microscopy and energy dispersive analysis of X-rays (CCSEMEDAX), and their carbon speciation was determined using scanning transmission X-ray microscopy and near-edge X-ray absorption fine structure spectroscopy (STXM/NEXAFS). Particle size distributions exposed to dry and humidified air employing

  16. The single scattering properties of the aerosol particles as aggregated spheres

    Science.gov (United States)

    Wu, Y.; Gu, X.; Cheng, T.; Xie, D.; Yu, T.; Chen, H.; Guo, J.

    2012-08-01

    The light scattering and absorption properties of anthropogenic aerosol particles such as soot aggregates are complicated in the temporal and spatial distribution, which introduce uncertainty of radiative forcing on global climate change. In order to study the single scattering properties of anthorpogenic aerosol particles, the structures of these aerosols such as soot paticles and soot-containing mixtures with the sulfate or organic matter, are simulated using the parallel diffusion limited aggregation algorithm (DLA) based on the transmission electron microscope images (TEM). Then, the single scattering properties of randomly oriented aerosols, such as scattering matrix, single scattering albedo (SSA), and asymmetry parameter (AP), are computed using the superposition T-matrix method. The comparisons of the single scattering properties of these specific types of clusters with different morphological and chemical factors such as fractal parameters, aspect ratio, monomer radius, mixture mode and refractive index, indicate that these different impact factors can respectively generate the significant influences on the single scattering properties of these aerosols. The results show that aspect ratio of circumscribed shape has relatively small effect on single scattering properties, for both differences of SSA and AP are less than 0.1. However, mixture modes of soot clusters with larger sulfate particles have remarkably important effects on the scattering and absorption properties of aggregated spheres, and SSA of those soot-containing mixtures are increased in proportion to the ratio of larger weakly absorbing attachments. Therefore, these complex aerosols come from man made pollution cannot be neglected in the aerosol retrievals. The study of the single scattering properties on these kinds of aggregated spheres is important and helpful in remote sensing observations and atmospheric radiation balance computations.

  17. The single scattering properties of the aerosol particles as aggregated spheres

    International Nuclear Information System (INIS)

    The light scattering and absorption properties of anthropogenic aerosol particles such as soot aggregates are complicated in the temporal and spatial distribution, which introduce uncertainty of radiative forcing on global climate change. In order to study the single scattering properties of anthorpogenic aerosol particles, the structures of these aerosols such as soot paticles and soot-containing mixtures with the sulfate or organic matter, are simulated using the parallel diffusion limited aggregation algorithm (DLA) based on the transmission electron microscope images (TEM). Then, the single scattering properties of randomly oriented aerosols, such as scattering matrix, single scattering albedo (SSA), and asymmetry parameter (AP), are computed using the superposition T-matrix method. The comparisons of the single scattering properties of these specific types of clusters with different morphological and chemical factors such as fractal parameters, aspect ratio, monomer radius, mixture mode and refractive index, indicate that these different impact factors can respectively generate the significant influences on the single scattering properties of these aerosols. The results show that aspect ratio of circumscribed shape has relatively small effect on single scattering properties, for both differences of SSA and AP are less than 0.1. However, mixture modes of soot clusters with larger sulfate particles have remarkably important effects on the scattering and absorption properties of aggregated spheres, and SSA of those soot-containing mixtures are increased in proportion to the ratio of larger weakly absorbing attachments. Therefore, these complex aerosols come from man made pollution cannot be neglected in the aerosol retrievals. The study of the single scattering properties on these kinds of aggregated spheres is important and helpful in remote sensing observations and atmospheric radiation balance computations.

  18. Charging of mesospheric aerosol particles: the role of photodetachment and photoionization from meteoric smoke and ice particles

    Directory of Open Access Journals (Sweden)

    M. Rapp

    2009-06-01

    Full Text Available Time constants for photodetachment, photoemission, and electron capture are considered for two classes of mesospheric aerosol particles, i.e., meteor smoke particles (MSPs and pure water ice particles. Assuming that MSPs consist of metal oxides like Fe2O3 or SiO, we find that during daytime conditions photodetachment by solar photons is up to 4 orders of magnitude faster than electron attachment such that MSPs cannot be negatively charged in the presence of sunlight. Rather, even photoemission can compete with electron capture unless the electron density becomes very large (>>1000 cm−3 such that MSPs should either be positively charged or neutral in the case of large electron densities. For pure water ice particles, however, both photodetachment and photoemission are negligible due to the wavelength characteristics of its absorption cross section and because the flux of solar photons has already dropped significantly at such short wavelengths. This means that water ice particles should normally be negatively charged. Hence, our results can readily explain the repeated observation of the coexistence of positive and negative aerosol particles in the polar summer mesopause, i.e., small MSPs should be positively charged and ice particles should be negatively charged. These results have further important implications for our understanding of the nucleation of mesospheric ice particles as well as for the interpretation of incoherent scatter radar observations of MSPs.

  19. Internally mixed soot, sulfates, and organic matter in aerosol particles from Mexico City

    Science.gov (United States)

    Adachi, K.; Buseck, P. R.

    2008-05-01

    Soot particles are major aerosol constituents that result from emissions of burning of fossil fuel and biomass. Because they both absorb sunlight and contribute to cloud formation, they are an influence on climate on local, regional, and global scales. It is therefore important to evaluate their optical and hygroscopic properties and those effects on the radiation budget. Those properties commonly change through reaction with other particles or gases, resulting in complex internal mixtures. Using transmission electron microscopy, we measured ~8000 particles (25 samples) with aerodynamic diameters from 0.05 to 0.3 μm that were collected in March 2006 from aircraft over Mexico City (MC) and adjacent areas. More than 50% of the particles consist of internally mixed soot, organic matter, and sulfate. Imaging combined with chemical analysis of individual particles show that many are coated, consist of aggregates, or both. Coatings on soot particles can amplify their light absorption, and coagulation with sulfates changes their hygroscopic properties, resulting in shorter lifetime. Our results suggest that a mixture of materials from multiple sources such as vehicles, power plants, and biomass burning occurs in individual particles, thereby increasing their complexity. Through changes in their optical and hygroscopic properties, internally mixed soot particles have a greater effect on the regional climate than uncoated soot particles. Moreover, soot occurs in more than 60% of all particles in the MC plumes, suggesting its important role in the formation of secondary aerosol particles.

  20. Response of dual-wavelength optical particle spectrometer (DWOPS) to well-defined aerosols

    International Nuclear Information System (INIS)

    Full text: It is a recognized fact that more information is contained in the spatial distribution of light scattered from a particle than is currently used in conventional spectrometers. Employing multiple detectors to study the elastically scattered light gives access to a description of a particle size, leading also to information on a particle's refractive index and maybe shape. The DWOPS measures and evaluates light scattered from an individual particle into four different angular ranges. This data corresponds to theoretically determinable instrument's responses for a given particle. A fit procedure finds the quadruple of theoretical values best matching the quadruple of measured values. Experiments with well-defined spherical, homogeneous aerosols will be reported and show that a unique particle sizing and also an unambiguous determination of the complex refractive indices of measured particles is possible. It must be mentioned that the particle measurement and evaluation of performance is based on the postulation of sphericity of aerosols in question, which may be assumed for many submicron atmospheric particles. The irregular shape of particles is an inherent difficulty in single optical particle spectrometry. Preliminary measurements with DWOPS are promissing in dealing with this issue. (author)

  1. Internally mixed soot, sulfates, and organic matter in aerosol particles from Mexico City

    Directory of Open Access Journals (Sweden)

    K. Adachi

    2008-05-01

    Full Text Available Soot particles are major aerosol constituents that result from emissions of burning of fossil fuel and biomass. Because they both absorb sunlight and contribute to cloud formation, they are an influence on climate on local, regional, and global scales. It is therefore important to evaluate their optical and hygroscopic properties and those effects on the radiation budget. Those properties commonly change through reaction with other particles or gases, resulting in complex internal mixtures. Using transmission electron microscopy, we measured ~8000 particles (25 samples with aerodynamic diameters from 0.05 to 0.3 μm that were collected in March 2006 from aircraft over Mexico City (MC and adjacent areas. More than 50% of the particles consist of internally mixed soot, organic matter, and sulfate. Imaging combined with chemical analysis of individual particles show that many are coated, consist of aggregates, or both. Coatings on soot particles can amplify their light absorption, and coagulation with sulfates changes their hygroscopic properties, resulting in shorter lifetime. Our results suggest that a mixture of materials from multiple sources such as vehicles, power plants, and biomass burning occurs in individual particles, thereby increasing their complexity. Through changes in their optical and hygroscopic properties, internally mixed soot particles have a greater effect on the regional climate than uncoated soot particles. Moreover, soot occurs in more than 60% of all particles in the MC plumes, suggesting its important role in the formation of secondary aerosol particles.

  2. Development and characterization of a single particle laser ablation mass spectrometer (SPLAM for organic aerosol studies

    Directory of Open Access Journals (Sweden)

    F. Gaie-Levrel

    2012-01-01

    Full Text Available A single particle instrument was developed for real-time analysis of organic aerosol. This instrument, named Single Particle Laser Ablation Mass Spectrometry (SPLAM, samples particles using an aerodynamic lens system for which the theoretical performances were calculated. At the outlet of this system, particle detection and sizing are realized by using two continuous diode lasers operating at λ = 403 nm. Polystyrene Latex (PSL, sodium chloride (NaCl and dioctylphtalate (DOP particles were used to characterize and calibrate optical detection of SPLAM. The optical detection limit (DL and detection efficiency (DE were determined using size-selected DOP particles. The DE ranges from 0.1 to 90% for 100 and 350 nm DOP particles respectively and the SPLAM instrument is able to detect and size-resolve particles as small as 110–120 nm. During optical detection, particle scattered light from the two diode lasers, is detected by two photomultipliers and the detected signals are used to trigger UV excimer laser (λ = 248 nm used for one-step laser desorption ionization (LDI of individual aerosol particles. The formed ions are analyzed by a 1 m linear time-of-flight mass spectrometer in order to access to the chemical composition of individual particles. The TOF-MS detection limit for gaseous aromatic compounds was determined to be 0.85 × 10−15 kg (∼4 × 103 molecules. DOP particles were also used to test the overall operation of the instrument. The analysis of a secondary organic aerosol, formed in a smog chamber by the ozonolysis of indene, is presented as a first application of the instrument. Single particle mass spectra were obtained with an effective hit rate of 8%. Some of these mass spectra were found to be very different from one particle to another possibly reflecting chemical differences within the investigated indene SOA particles. Our study shows that an exhaustive statistical analysis, over hundreds of particles

  3. The effect of phase partitioning of semivolatile compounds on the measured CCN activity of aerosol particles

    Science.gov (United States)

    Romakkaniemi, S.; Jaatinen, A.; Laaksonen, A.; Nenes, A.; Raatikainen, T.

    2013-09-01

    The effect of inorganic semivolatile aerosol compounds on the CCN activity of aerosol particles was studied by using a computational model for a DMT-CCN counter, a cloud parcel model for condensation kinetics and experiments to quantify the modelled results. Concentrations of water vapour and semivolatiles as well as aerosol trajectories in the CCN column were calculated by a computational fluid dynamics model. These trajectories and vapour concentrations were then used as an input for the cloud parcel model to simulate mass transfer kinetics of water and semivolatiles between aerosol particles and the gas phase. Two different questions were studied: (1) how big fraction of semivolatiles is evaporated from particles before activation in the CCN counter? (2) How much the CCN activity can be increased due to condensation of semivolatiles prior to the maximum water supersaturation in the case of high semivolatile concentration in the gas phase? The results show that, to increase the CCN activity of aerosol particles, a very high gas phase concentration (as compared to typical ambient conditions) is needed. We used nitric acid as a test compound. A concentration of several ppb or higher is needed for measurable effect. In the case of particle evaporation, we used ammonium nitrate as a test compound and found that it partially evaporates before maximum supersaturation is reached in the CCN counter, thus causing an underestimation of CCN activity. The effect of evaporation is clearly visible in all supersaturations, leading to an underestimation of the critical dry diameter by 10 to 15 nanometres in the case of ammonium nitrate particles in different supersaturations. This result was also confirmed by measurements in supersaturations between 0.1 and 0.7%.

  4. The effect of phase partitioning of semivolatile compounds on the measured CCN activity of aerosol particles

    Directory of Open Access Journals (Sweden)

    S. Romakkaniemi

    2013-09-01

    Full Text Available The effect of inorganic semivolatile aerosol compounds on the CCN activity of aerosol particles was studied by using a computational model for a DMT-CCN counter, a cloud parcel model for condensation kinetics and experiments to quantify the modelled results. Concentrations of water vapour and semivolatiles as well as aerosol trajectories in the CCN column were calculated by a computational fluid dynamics model. These trajectories and vapour concentrations were then used as an input for the cloud parcel model to simulate mass transfer kinetics of water and semivolatiles between aerosol particles and the gas phase. Two different questions were studied: (1 how big fraction of semivolatiles is evaporated from particles before activation in the CCN counter? (2 How much the CCN activity can be increased due to condensation of semivolatiles prior to the maximum water supersaturation in the case of high semivolatile concentration in the gas phase? The results show that, to increase the CCN activity of aerosol particles, a very high gas phase concentration (as compared to typical ambient conditions is needed. We used nitric acid as a test compound. A concentration of several ppb or higher is needed for measurable effect. In the case of particle evaporation, we used ammonium nitrate as a test compound and found that it partially evaporates before maximum supersaturation is reached in the CCN counter, thus causing an underestimation of CCN activity. The effect of evaporation is clearly visible in all supersaturations, leading to an underestimation of the critical dry diameter by 10 to 15 nanometres in the case of ammonium nitrate particles in different supersaturations. This result was also confirmed by measurements in supersaturations between 0.1 and 0.7%.

  5. MATRIX (Multiconfiguration Aerosol TRacker of mIXing state: an aerosol microphysical module for global atmospheric models

    Directory of Open Access Journals (Sweden)

    S. E. Bauer

    2008-05-01

    Full Text Available A new aerosol microphysical module MATRIX, the Multiconfiguation Aerosol TRacker of mIXing state, and its application in the Goddard Institute for Space Studies (GISS climate model (ModelE is described. This module, which is based on the quadrature method of moments (QMOM, represents nucleation, condensation, coagulation, internal and external mixing, and cloud-drop activation and provides aerosol particle mass and number concentration and particle size information for up to 16 mixed-mode aerosol populations. Internal and external mixing among aerosol components sulfate, nitrate, ammonium, carbonaceous aerosols, dust and sea-salt particles are represented. The solubility of each aerosol mode, which is explicitly calculated based on its soluble and insoluble components, enables calculation of the dependence of cloud drop activation on the microphysical characterization of multiple soluble modes. A detailed model description and results of box-model simulations of various mode configurations are presented. The number concentration of aerosol particles activated to cloud drops depends on the mode configuration. Simulations on the global scale with the GISS climate model are evaluated against aircraft and station measurements of aerosol mass and number concentration and particle size. The model accurately captures the observed size distributions in the aitken and accumulation modes up to particle diameter 1 μm, in which sulfate, nitrate, black and organic carbon are predominantly located; however the model underestimates coarse-mode number concentration and size, especially in the marine environment.

  6. Simulating Deposition of Aerosol Particles on Single Fiber Surface

    Institute of Scientific and Technical Information of China (English)

    FU Hai-ming; ZHU Hui

    2009-01-01

    The stochastic simulation method, based on the concept of control window and the numerical solution of the Langevin equation, is applied to solve the deposition problem of particles from the flowing suspensions onto a fiber collector. Using the Kuwabara model to characterize the flow field, the effects of Stokes number, interception parameter, packing density, particle size distribution on the collection efficiency, and the deposition morphology of particles onto a collector areexamined. The morphology of deposit obtained in the simulated results agrees well with experimental observations. The estimation of the initial collection efficiency through the simulations considers that the deposited particles are in good agreement with published experimental data. In addition, the collection efficiency of particles increases in a wider particle size distribution region.

  7. Source apportionment of single aerosol particles in the atmosphere of Shanghai city

    International Nuclear Information System (INIS)

    A nuclear microprobe with high spatial resolution and high analytical sensitivity was applied to analyze atmospheric aerosol at five monitoring sites in Shanghai city. Meantime, a new pattern recognition technique, which used the micro-PIXE spectrum of a single aerosol particle as its fingerprint, was developed to identify the origin of the particle. The results showed that the major contributors to the atmosphere pollution were soil dust (31.6%), building dust (30.8%), and the next were vehicle exhaust (13.7%), metallurgic industry excrements (5.6%), oil combustion (5%) and coal combustion (2.3%). Besides these, about 10% of the particles could not be identified. Based on the cluster analysis of these particles, they could be divided into soil dust, building dust and metallurgic industry excrements. Moreover, some new pollution sources from tyres and chemical plants were also revealed

  8. Source apportionment of single aerosol particles in the atmosphere of Shanghai city

    Institute of Scientific and Technical Information of China (English)

    2001-01-01

    A nuclear microprobe with high spatial resolution and high analyti cal sensitivity was applied to analyze atmospheric aerosol at five monitoring sites in Shanghai city. Meantime, a new pattern recognition technique, which used the micro PIXE spectrum of a single aerosol particle as its fingerprint, was developed to identify the origin of the particle. The results showed that the major contributors to the at mosphere pollution were soil dust (31.6%), building dust (30.8%), and the next were vehicle exhaust (13.7%), metallurgic industry excrements (5.6%), oil combustion (5%) and coal combustion (2.3%). Besides these, about 10% of the particles could not be identified. Based on the cluster analysis of these particles, they could be divided into eight groups. By inference, they might belong to some sub-pollution sources from soil dust, building dust and metallurgic industry excrements. Moreover, some new pollution sources from tyres and chemical plants were also revealed.

  9. A Novel Aerosol Method for the Production of Hydrogel Particles

    Directory of Open Access Journals (Sweden)

    Diana Guzman-Villanueva

    2011-01-01

    Full Text Available A novel method of generating hydrogel particles for various applications including drug delivery purposes was developed. This method is based on the production of hydrogel particles from sprayed polymeric nano/microdroplets obtained by a nebulization process that is immediately followed by gelation in a crosslinking fluid. In this study, particle synthesis parameters such as type of nebulizer, type of crosslinker, air pressure, and polymer concentration were investigated for their impact on the mean particle size, swelling behavior, and morphology of the developed particles. Spherical alginate-based hydrogel particles with a mean particle size in the range from 842 to 886 nm were obtained. Using statistical analysis of the factorial design of experiment it was found that the main factors influencing the size and swelling values of the particles are the alginate concentration and the air pressure. Thus, it was demonstrated that the method described in the current study is promising for the generation of hydrogel particles and it constitutes a relatively simple and low-cost system.

  10. MISR Dark Water aerosol retrievals: operational algorithm sensitivity to particle non-sphericity

    Directory of Open Access Journals (Sweden)

    O. V. Kalashnikova

    2013-02-01

    Full Text Available The aim of this study is to theoretically investigate the sensitivity of the Multi-angle Imaging SpectroRadiometer (MISR operational (Version 22 Dark Water retrieval algorithm to aerosol non-sphericity over the global oceans under actual observing conditions, accounting for current algorithm assumptions. Non-spherical (dust aerosol models, which were introduced in Version 16 of the MISR aerosol