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31.
Secondary organic aerosol formation from anthropogenic air pollution
Rainer Volkamer, Jose L. Jimenez, F. M. San Martini, Katja Džepina, Q. Zhang, Dara Salcedo, Luisa T. Molina, D. Worsnop, 2006, izvirni znanstveni članek

Opis: The atmospheric chemistry of volatile organic compounds (VOCs) in urban areas results in the formation of 'photochemical smog', including secondary organic aerosol (SOA). State-of-the-art SOA models parameterize the results of simulation chamber experiments that bracket the conditions found in the polluted urban atmosphere. Here we show that in the real urban atmosphere reactive anthropogenic VOCs (AVOCs) produce much larger amounts of SOA than these models predict, even shortly after sunrise. Contrary to current belief, a significant fraction of the excess SOA is formed from first-generation AVOC oxidation products. Global models deem AVOCs a very minor contributor to SOA compared to biogenic VOCs (BVOCs). If our results are extrapolated to other urban areas, AVOCs could be responsible for additional 3 - 25 Tg yr(-1) SOA production globally, and cause up to - 0.1 W m(-2) additional top-of-the-atmosphere radiative cooling.
Najdeno v: ključnih besedah
Ključne besede: atmospheric aerosol, atmospheric chemistry, volatile organic compounds, secondary organic aerosols
Objavljeno: 12.04.2021; Ogledov: 188; Prenosov: 0
.pdf Polno besedilo (638,71 KB)

32.
Sources and transformations of particle-bound polycyclic aromatic hydrocarbons in Mexico City
L. C. Marr, Katja Džepina, Jose L. Jimenez, F. Reisen, H. L. Bethel, Janet Arey, J. S. Gaffney, N. A. Marley, Luisa T. Molina, Mario J. Molina, 2006, izvirni znanstveni članek

Opis: Understanding sources, concentrations, and transformations of polycyclic aromatic hydrocarbons (PAHs) in the atmosphere is important because of their potent mutagenicity and carcinogenicity. The measurement of particle-bound PAHs by three different methods during the Mexico City Metropolitan Area field campaign in April 2003 presents a unique opportunity for characterization of these compounds and intercomparison of the methods. The three methods are ( 1) collection and analysis of bulk samples for time-integrated gas- and particle-phase speciation by gas chromatography/ mass spectrometry; ( 2) aerosol photoionization for fast detection of PAHs on particles' surfaces; and ( 3) aerosol mass spectrometry for fast analysis of size and chemical composition. This research represents the first time aerosol mass spectrometry has been used to measure ambient PAH concentrations and the first time that fast, real-time methods have been used to quantify PAHs alongside traditional filter-based measurements in an extended field campaign. Speciated PAH measurements suggest that motor vehicles and garbage and wood burning are important sources in Mexico City. The diurnal concentration patterns captured by aerosol photoionization and aerosol mass spectrometry are generally consistent. Ambient concentrations of particle-phase PAHs typically peak at similar to 110 ng m(-3) during the morning rush hour and rapidly decay due to changes in source activity patterns and dilution as the boundary layer rises, although surface-bound PAH concentrations decay faster. The more rapid decrease in surface versus bulk PAH concentrations during the late morning suggests that freshly emitted combustion-related particles are quickly coated by secondary aerosol material in Mexico City's atmosphere and may also be transformed by heterogeneous reactions.
Najdeno v: ključnih besedah
Povzetek najdenega: ...by gas chromatography/ mass spectrometry; ( 2) aerosol photoionization for fast detection of PAHs on...
Ključne besede: aerosol mass-spectrometer, aerodynamic diameter measurements, oxygenated organic aerosols, relative rate constants
Objavljeno: 12.04.2021; Ogledov: 224; Prenosov: 0
.pdf Polno besedilo (1,06 MB)

33.
Characterization of ambient aerosols in Mexico City during the MCMA-2003 campaign with aerosol mass spectrometry
Dara Salcedo, T. B. Onasch, Katja Džepina, M. R. Canagaratna, Qi Zhang, J. A. Huffman, P. F. DeCarlo, J. Jayne, P. Mortimer, D. Worsnop, 2006, izvirni znanstveni članek

Opis: An Aerodyne Aerosol Mass Spectrometer (AMS) was deployed at the CENICA Supersite, during the Mexico City Metropolitan Area field study (MCMA-2003) from 31 March-4 May 2003 to investigate particle concentrations, sources, and processes. The AMS provides real time information on mass concentration and composition of the non-refractory species in particulate matter less than 1 mu m (NR-PM1) with high time and size-resolution. In order to account for the refractory material in the aerosol, we also present estimates of Black Carbon (BC) using an aethalometer and an estimate of the aerosol soil component obtained from Proton-Induced X-ray Emission Spectrometry (PIXE) analysis of impactor substrates. Comparisons of AMS + BC + soil mass concentration with other collocated particle instruments (a LASAIR Optical Particle Counter, a PM2.5 Tapered Element Oscillating Microbalance (TEOM), and a PM2.5 DustTrak Aerosol Monitor) show that the AMS + BC + soil mass concentration is consistent with the total PM2.5 mass concentration during MCMA-2003 within the combined uncertainties. In Mexico City, the organic fraction of the estimated PM2.5 at CENICA represents, on average, 54.6% (standard deviation sigma=10%) of the mass, with the rest consisting of inorganic compounds ( mainly ammonium nitrate and sulfate/ammonium salts), BC, and soil. Inorganic compounds represent 27.5% of PM2.5 (sigma=10%); BC mass concentration is about 11% (sigma=4%); while soil represents about 6.9% (sigma=4%). Size distributions are presented for the AMS species; they show an accumulation mode that contains mainly oxygenated organic and secondary inorganic compounds. The organic size distributions also contain a small organic particle mode that is likely indicative of fresh traffic emissions; small particle modes exist for the inorganic species as well. Evidence suggests that the organic and inorganic species are not always internally mixed, especially in the small modes. The aerosol seems to be neutralized most of the time; however, there were some periods when there was not enough ammonium to completely neutralize the nitrate, chloride and sulfate present. The diurnal cycle and size distributions of nitrate suggest local photochemical production. On the other hand, sulfate appears to be produced on a regional scale. There are indications of new particle formation and growth events when concentrations of SO2 were high. Although the sources of chloride are not clear, this species seems to condense as ammonium chloride early in the morning and to evaporate as the temperature increases and RH decreases. The total and speciated mass concentrations and diurnal cycles measured during MCMA-2003 are similar to measurements during a previous field campaign at a nearby location.
Najdeno v: ključnih besedah
Ključne besede: aerosol mass-spectrometer, atmospheric aerosol, atmospheric chemistry, atmospheric physics
Objavljeno: 12.04.2021; Ogledov: 229; Prenosov: 0
.pdf Polno besedilo (2,53 MB)

34.
Intercomparison and characterization of 23 Aethalometers under laboratory and ambient air conditions:
Björn Briel, Vadimas Dudoitis, Javier Fernández-García, Paul Buckley, Sascha Pfeifer, Maria Cruz Minguillon, Thomas Müller, Luka Drinovec, Andrea Cuesta-Mosquera, Griša Močnik, 2021, izvirni znanstveni članek

Opis: Aerosolized black carbon is monitored worldwide to quantify its impact on air quality and climate. Given its importance, measurements of black carbon mass concentrations must be conducted with instruments operating in quality-checked and ensured conditions to generate data which are reliable and comparable temporally and geographically. In this study, we report the results from the largest characterization and intercomparison of filter-based absorption photometers, the Aethalometer model AE33, belonging to several European monitoring networks. Under controlled laboratory conditions, a total of 23 instruments measured mass concentrations of black carbon from three well-characterized aerosol sources: synthetic soot, nigrosin particles, and ambient air from the urban background of Leipzig, Germany. The objective was to investigate the individual performance of the instruments and their comparability; we analyzed the response of the instruments to the different aerosol sources and the impact caused by the use of obsolete filter materials and the application of maintenance activities. Differences in the instrument-to-instrument variabilities from equivalent black carbon (eBC) concentrations reported at 880 nm were determined before maintenance activities (for soot measurements, average deviation from total least square regression was −2.0 % and the range −16 % to 7 %; for nigrosin measurements, average deviation was 0.4 % and the range −15 % to 17 %), and after they were carried out (for soot measurements, average deviation was −1.0 % and the range −14 % to 8 %; for nigrosin measurements, the average deviation was 0.5 % and the range −12 % to 15 %). The deviations are in most of the cases explained by the type of filter material employed by the instruments, the total particle load on the filter, and the flow calibration. The results of this intercomparison activity show that relatively small unit-to-unit variability of AE33-based particle light absorbing measurements is possible with well-maintained instruments. It is crucial to follow the guidelines for maintenance activities and the use of the proper filter tape in the AE33 to ensure high quality and comparable black carbon (BC) measurements among international observational networks.
Najdeno v: ključnih besedah
Povzetek najdenega: ... Aerosolized black carbon is monitored worldwide to quantify...
Ključne besede: black carbon, aerosol, absorption, filter absorption photometer, aethaloemter
Objavljeno: 03.05.2021; Ogledov: 219; Prenosov: 0
.pdf Polno besedilo (5,57 MB)

35.
Molekularna karakterizacija lebdećih čestica slobodne troposfere sa Opservatorija Pico planine
Sumit Kumar, J. A. Perlinger, D. Helmig, J. Hueber, Swarup China, B. Zhang, R. Chris Owen, Katja Džepina, Claudio Mazzoleni, Paulo Fialho, 2017, objavljeni povzetek znanstvenega prispevka na konferenci

Opis: Long-range transported free tropospheric aerosol was sampled at the PMO (38°28’15’’N, 28°24’14’’W; 2225 m amsl) on Pico Island of the Azores in the North Atlantic. Filter-collected aerosol during summer 2012 was analysed for organic and elemental carbon, and inorganic ions. The average aerosol ambient concentration was 0.9 µg m-3. Organic aerosol contributed the majority of mass (57%), followed by sulphate (21%) and nitrate (17%). Filter-collected aerosol was positively correlated with on-line aerosol measurements of black carbon, light scattering and number concentration. Water-soluble organic compounds (WSOC) from 9/24 and 9/25 samples collected during a pollution event were analysed with ultrahigh-resolution FT-ICR MS. FLEXPART analysis showed the air masses were very aged (>12 days). ~4000 molecular formulas were assigned to each of the mass spectra between m/z 100-1000. The majority of the assigned molecular formulas have unsaturated structures with CHO and CHNO elemental compositions. WSOC have an average O/C of ~0.45, relatively low compared to O/C of other aged aerosol, which might be the result of evaporation and fragmentation during long-range transport. The increase in aerosol loading during 9/24 was linked to biomass burning emissions from North America by FLEXPART and MODIS fire counts. This was confirmed with WSOC biomass burning markers and with the morphology and mixing state of particles as determined by SEM. The presence of markers characteristic of aqueous-phase reactions of biomass burning phenolic species suggests that the aerosol collected at Pico had undergone cloud processing. The air masses on 9/25 were more aged (~15 days) and influenced by marine emissions, as indicated by organosulphates and species characteristic for marine aerosol (e.g. fatty acids). The change in air masses for the two samples was corroborated by the changes in ozone, ethane, propane, morphology of particles, as well as by FLEXPART. In this presentation we will presents the first detailed molecular characterization of free tropospheric aged aerosol intercepted at the PMO.
Najdeno v: ključnih besedah
Povzetek najdenega: ...Long-range transported free tropospheric aerosol was sampled at the PMO (38°28’15’’N, 28°24’14’’W;...
Ključne besede: Atmospheric aerosol, Free troposphere, Mass spectrometry, Pico mountain observatory
Objavljeno: 26.05.2021; Ogledov: 168; Prenosov: 0
.pdf Polno besedilo (8,36 MB)

36.
Chemical characterization of atmospheric aerosols in the Sarajevo Canton
Katja Džepina, 2018, objavljeni povzetek znanstvenega prispevka na konferenci (vabljeno predavanje)

Opis: The World Health Organization (WHO) identified air pollution as the world’s largest single environmental health risk causing seven million deaths per year, one in eight deaths globally. Of particular concern are heavily polluted and understudied urban centres: while thousands of scientific papers have been published on air quality of the cities such as London, UK and Los Angeles, USA, only 41 papers exist on the top 10 globally most polluted cities. Sarajevo, the capital of Bosnia and Herzegovina (B&H), is one of urban centres which often experiences low air quality due to the extensive use of non-renewable energy sources and geographical location. For example, in Sarajevo during 2010, an annual average concentration of particulate matter (PM) with a diameter smaller than 10 µm (PM10) was 50 µg/m3, a value 2.5x higer than the recommended WHO guidelines value of 20 µg/m3. Sarajevo Canton Winter Field Campaign 2017-2018 (SAFICA) took place in the Sarajevo Canton during the cold winter season of 2017 – 2018 (Dec 4, 2017 – Mar 15, 2018), the period historically characterized with the lowest air quality according to the available data. SAFICA project was lead by Federal hydrometeorological Institute of B&H, Institute of Public Health of the Sarajevo Canton, University of Sarajevo and University of Rijeka, and field measurements took place at three urban locations within the city of Sarajevo (Otoka, Pofalići i Bjelave) i one remote location (Ivan Sedlo mountain ridge). In this presentation, the basics of anthropogenic air pollution and its global influece on the air quality will be explained. Particular attention will be given to the atmospheric PM or aerosols, and aerosols formation mechanisms and the importance of their characteristics such as atmospheric concentration, size and chemical composition will be explained. Also, the reasons for the adverse effects of aerosols on human health and the correlation of atmospheric fine PM (PM2.5) concentrations and human mortality will be explained. Finally, preliminary results of SAFICA measurements campaign will be presented and compared with those from other global urban centers.
Najdeno v: ključnih besedah
Povzetek najdenega: ...atmospheric aerosol, Sarajevo, urban air pollution, SAFICA 2018...
Ključne besede: atmospheric aerosol, Sarajevo, urban air pollution, SAFICA 2018
Objavljeno: 26.05.2021; Ogledov: 163; Prenosov: 0
.pdf Polno besedilo (6,65 MB)

37.
WRF-Chem simulations of Saharan dust outbreak episode at North Adriatic coast
Katja Džepina, 2018, prispevek na konferenci brez natisa

Najdeno v: ključnih besedah
Povzetek najdenega: ...Atmospheric aerosol, Sahara dust, WRF-Chem, Northern Adriatic...
Ključne besede: Atmospheric aerosol, Sahara dust, WRF-Chem, Northern Adriatic
Objavljeno: 28.05.2021; Ogledov: 181; Prenosov: 0
.pdf Polno besedilo (24,83 MB)

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