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61.
Real-time characterization and source apportionment of fine particulate matter in the Delhi megacity area during late winter
Vipul Lalchandan, Varun Kumar, Anna Tobler, M.T. Navaneeth, Suneeti Mishra, J. G. Slowik, Deepika Bhattu, Pragati Rai, Rangu Satish, Dilip Ganguly, Tiwari Tiwari, Neeraj Rastogi, Tiwari Sashi, Griša Močnik, André S. H. Prévôt, Sachchida Tripathi, 2021, izvirni znanstveni članek

Opis: National Capital Region (NCR) encompassing New Delhi is one of the most polluted urban metropolitan areas in the world. Real-time chemical characterization of fine particulate matter (PM1 and PM2.5) was carried out using three aerosol mass spectrometers, two aethalometers, and one single particle soot photometer (SP2) at two sites in Delhi (urban) and one site located ~40 km downwind of Delhi, during January-March, 2018. The campaign mean PM2.5 (NR-PM2.5 + BC) concentrations at the two urban sites were 153.8±109.4 μg.m-3 and 127.8±83.2 μg.m-3, respectively, whereas PM1 (NR-PM1 + BC) was 72.3 ± 44.0 μg.m-3 at the downwind site. PM2.5 particles were composed mostly of organics (43-44)% followed by chloride (14-17)%, ammonium (9-11)%, nitrate (9%), sulfate (8-10)%, and black carbon (11-16)%, whereas PM1 particles were composed of 47% organics, 13% sulfate as well as ammonium, 11% nitrate as well as chloride, and 5% black carbon. Organic aerosol (OA) source apportionment was done using positive matrix factorization (PMF), solved using an advanced multi-linear engine (ME-2) model. Highly mass-resolved OA mass spectra at one urban and downwind site were factorized into three primary organic aerosol (POA) factors including one traffic-related and two solid-fuel combustion (SFC), and three oxidized OA (OOA) factors. Whereas unit mass resolution OA at the other urban site was factorized into two POA factors related to traffic and SFC, and one OOA factor. OOA constituted a majority of the total OA mass (45-55)% with maximum contribution during afternoon hours ~(70-80)%. Significant differences in the absolute OOA concentration between the two urban sites indicated the influence of local emissions on the oxidized OA formation. Similar PM chemical composition, diurnal and temporal variations at the three sites suggest similar type of sources affecting the particulate pollution in Delhi and adjoining cities, but variability in mass concentration suggest more local influence than regional.
Ključne besede: source apportionment, air pollution, particulate matter, Delhi
Objavljeno v RUNG: 25.01.2021; Ogledov: 3506; Prenosov: 0
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62.
Aircraft vertical profiles during summertime regional and Saharan dust scenarios over the north-western Mediterranean basin: aerosol optical and physical properties
Jesús Yus-Díez, Marina Ealo, Marco Pandolfi, Noemi Perez, Gloria Titos, Griša Močnik, Xavier Querol, A. Alastuey, 2021, izvirni znanstveni članek

Opis: Accurate measurements of the horizontal and vertical distribution of atmospheric aerosol particle optical properties are key for a better understanding of their impact on the climate. Here we present the results of a measurement campaign based on instrumented flights over north-eastern Spain. We measured vertical profiles of size-segregated atmospheric particulate matter (PM) mass concentrations and multi-wavelength scattering and absorption coefficients in the western Mediterranean basin (WMB). The campaign took place during typical summer conditions, characterized by the development of a vertical multi-layer structure, under both summer regional pollution episodes (REGs) and Saharan dust events (SDEs). REG patterns in the region form under high insolation and scarce precipitation in summer, favouring layering of highly aged fine-PM strata in the lower few kma.s.l. The REG scenario prevailed during the entire measurement campaign. Additionally, African dust outbreaks and plumes from northern African wildfires influenced the study area. The vertical profiles of climate-relevant intensive optical parameters such as single-scattering albedo (SSA); the asymmetry parameter (g); scattering, absorption and SSA Ångström exponents (SAE, AAE and SSAAE); and PM mass scattering and absorption cross sections (MSC and MAC) were derived from the measurements. Moreover, we compared the aircraft measurements with those performed at two GAW–ACTRIS (Global Atmosphere Watch–Aerosol, Clouds and Trace Gases) surface measurement stations located in north-eastern Spain, namely Montseny (MSY; regional background) and Montsec d'Ares (MSA; remote site). Airborne in situ measurements and ceilometer ground-based remote measurements identified aerosol air masses at altitudes up to more than 3.5 kma.s.l. The vertical profiles of the optical properties markedly changed according to the prevailing atmospheric scenarios. During SDE the SAE was low along the profiles, reaching values < 1.0 in the dust layers. Correspondingly, SSAAE was negative, and AAE reached values up to 2.0–2.5, as a consequence of the UV absorption increased by the presence of the coarse dust particles. During REG, the SAE increased to > 2.0, and the asymmetry parameter g was rather low (0.5–0.6) due to the prevalence of fine PM, which was characterized by an AAE close to 1.0, suggesting a fossil fuel combustion origin. During REG, some of the layers featured larger AAE (> 1.5), relatively low SSA at 525 nm (< 0.85) and high MSC (> 9 m2 g−1) and were associated with the influence of PM from wildfires. Overall, the SSA and MSC near the ground ranged around 0.85 and 3 m2 g−1, respectively, and increased at higher altitudes, reaching values above 0.95 and up to 9 m2 g−1. The PM, MSC and MAC were on average larger during REG compared to SDE due to the larger scattering and absorption efficiency of fine PM compared with dust. The SSA and MSC had quite similar vertical profiles and often both increased with height indicating the progressive shift toward PM with a larger scattering efficiency with altitude. This study contributes to our understanding of regional-aerosol vertical distribution and optical properties in the WMB, and the results will be useful for improving future climate projections and remote sensing or satellite retrieval algorithms.
Ključne besede: aerosol, climate change, Saharan dust, black carbon, aerosol absorption, aerosol scattering
Objavljeno v RUNG: 14.01.2021; Ogledov: 2553; Prenosov: 0
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63.
Hidden black carbon air pollution in hilly rural areas - a case study of Dinaric depression
Kristina Glojek, Asta Gregorič, Griša Močnik, Andrea Cuesta-Mosquera, A. Wiedensohler, Luka Drinovec, Matej Ogrin, 2020, izvirni znanstveni članek

Opis: Air pollution is not an exclusively urban problem as wood burning is a widespread practice in rural areas. As we lack information on the air quality situation in rural mountainous regions, our aim is to examine equivalent black carbon (eBC) pollution in a typical rural karst area in the settlement of Loški Potok (Slovenia). eBC mass concentrations were measured by Aethalometer (AE-33) at two sites in Retje karst depression. The rural village station was located at the bottom of the karst depression whereas the rural background station was positioned at the top of the hill. We showthe diurnal variation of equivalent black carbon mass concentrations for different seasons. In the populated karst depression, the major source of eBC pollution are households using wood as a heating fuel reaching the highest mass concentrations in winter. Diurnal pattern of eBC from biomass burning and traffic differ due to different source activity and it is influenced by typical formation of a cold air pool from late afternoon until late morning, restricting the dispersion of local emissions. The large difference in mass concentrations between the lowest part of the village (rural station) and the top of the hill (rural background station) indicates that in a vertically stratified and stable atmosphere local sources of black carbon have a major impact onair quality conditions in the area studied. Since in Alpine and Dinaric regions there are many similar inhabited areas, we can expect similar air quality conditions also in other rural hilly areas with limited self-cleaning air capacity.
Ključne besede: air pollution, black carbon, hidden geographies, diurnal variation, biomass burning, relief depressions, Loški Potok, Slovenia
Objavljeno v RUNG: 04.01.2021; Ogledov: 2485; Prenosov: 0
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64.
A single-beam photothermal interferometer for in situ measurements of aerosol light absorption
Bradley Visser, Jannis Röhrbein, Peter Steigmeier, Luka Drinovec, Griša Močnik, Ernest Weingartner, 2020, izvirni znanstveni članek

Opis: We have developed a novel single-beam photothermal interferometer and present here its application for the measurement of aerosol light absorption. The use of only a single laser beam allows for a compact optical set-up and significantly easier alignment compared to standard dual-beam photothermal interferometers, making it ideal for field measurements. Due to a unique configuration of the reference interferometer arm, light absorption by aerosols can be determined directly – even in the presence of light-absorbing gases. The instrument can be calibrated directly with light-absorbing gases, such as NO2, and can be used to calibrate other light absorption instruments. The detection limits (1σ) for absorption for 10 and 60 s averaging times were determined to be 14.6 and 7.4 Mm−1, respectively, which for a mass absorption cross section of 10 m2 g−1 leads to equivalent black carbon concentration detection limits of 1460 and 740 ng m−3, respectively. The detection limit could be reduced further by improvements to the isolation of the instrument and the signal detection and processing schemes employed.
Ključne besede: aerosol, aerosol absorption, black carbon, photo-thermal interferometer, climate change
Objavljeno v RUNG: 29.12.2020; Ogledov: 2737; Prenosov: 74
.pdf Celotno besedilo (2,44 MB)

65.
Performance of microAethalometers: Real-world Field Intercomparisons from Multiple Mobile Measurement Campaigns in Different Atmospheric Environments
Honey Alas, Thomas Mueller, Kay Weinhold, Sascha Pfeifer, Kristina Glojek, Asta Gregorič, Griša Močnik, Luka Drinovec, Francesca Costabile, Martina Ristorini, A. Wiedensohler, 2020, izvirni znanstveni članek

Opis: Small aethalometers are frequently used to measure equivalent black carbon (eBC) mass concentrations in the context of personal exposure and air pollution mapping through mobile measurements (MM). The most widely used is the microAethalometer (AE51). Its performance in the laboratory and field is well documented, however, there is not sufficient data in the context of its performance in different environments. In this investigation, we present the characterization of the performance of the AE51 through field unit-to-unit intercomparisons (IC), and against a reference absorption photometer from three MM campaigns conducted in drastically different environments. Five IC parameters were considered: i) study area, ii) location of IC, iii) time of day, iv) duration of IC, and v) correction for the filter-loading effect. We can conclude that it is crucial where and how long the IC have been performed in terms of the correlation between the mobile and reference instruments. Better correlations (R2 > 0.8, slope = 0.8) are achieved for IC performed in rural, and background areas for more than 10 minutes. In locations with more homogenous atmosphere, the correction of the loading effect improved the correlation between the mobile and reference instruments. In addition, a newer microAethalometer model (MA200) was characterized in the field under extreme cold conditions and correlated against another MA200 (R2 > 0.8, slope ≈ 1.0), AE51(R2 > 0.9, slope ≈ 0.9), and a stationary Aethalometer (AE33) across all wavelengths (R2 > 0.8, slope ≈ 0.7). For MA200, the loading effect was more pronounced, especially at the lower wavelengths, hence the correction of the loading effect is essential to improve the correlation against the AE33. The MA200 and AE51 proved to be robust and dependable portable instruments for MM applications. Real-world quality assurance of these instruments should be performed through field IC against reference instruments with longer durations in areas of slowly changing eBC concentration.
Ključne besede: Portable instruments, Mobile monitoring, Black carbon, Instrument intercomparisons
Objavljeno v RUNG: 15.09.2020; Ogledov: 2769; Prenosov: 184
.pdf Celotno besedilo (3,54 MB)

66.
Photo-thermal interferometer
Luka Drinovec, Griša Močnik, 2020, patent

Opis: A photo-thermal interferometer for measuring the light absorption of an aerosol or gas comprises a first laser source emitting a laser beam and a beam splitter adapted to divide the laser beam into a probe beam and a reference beam. The interferometer further comprises first optical elements which are adapted to direct the probe beam such that it passes through the aerosol and interferes with the reference beam thereafter thereby causing interference patterns. A detector detects the interference patterns. The interferometer further comprises a second laser source configured to emit a pump beam for transferring energy to the aerosol. Second optical elements are adapted to direct the pump beam such that it overlaps with the probe beam at least partially in the aerosol or gas. At least one of the second optical elements modifying the pump beam is an axicon.
Ključne besede: aerosol, absorption, black carbon
Objavljeno v RUNG: 15.09.2020; Ogledov: 3078; Prenosov: 0
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67.
Air quality and climate change - how smart can the cities be?
Griša Močnik, Matevž Lenarčič, 2020, vabljeno predavanje na konferenci brez natisa

Opis: What starts as an air quality problem in urban areas, ends up as a climate change problem globally. Emissions from cities and the power generating facilities powering the cities have local, regional and global effects. We show examples spanning these scales with very practical advice on how to start abatement locally.
Ključne besede: air quality, climate change, black carbon, aerosol, co2, smart city
Objavljeno v RUNG: 11.09.2020; Ogledov: 3361; Prenosov: 0
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68.
The new instrument using a TC–BC (total carbon–black carbon) method for the online measurement of carbonaceous aerosols
Martin Rigler, Luka Drinovec, Gašper Lavrič, Anastasia Vlachou, André S. H. Prévôt, Jean-Luc Jaffrezo, Iasonas Stavroulas, Jean Sciare, Judita Burger, Irena Krajnc, Janja Turšič, Anthony D. A. Hansen, Griša Močnik, 2020, izvirni znanstveni članek

Opis: We present a newly developed total carbon analyzer (TCA08) and a method for online speciation of carbonaceous aerosol with a high time resolution. The total carbon content is determined by flash heating of a sample collected on a quartz-fiber filter with a time base between 20 min and 24 h. The limit of detection is approximately 0.3 µg C, which corresponds to a concentration of 0.3 µg C m−3 at a sample flow rate of 16.7 L min−1 and a 1 h sampling time base. The concentration of particulate equivalent organic carbon (OC) is determined by subtracting black carbon concentration, concurrently measured optically by an Aethalometer®, from the total carbon concentration measured by the TCA08. The combination of the TCA08 and Aethalometer (AE33) is an easy-to-deploy and low-maintenance continuous measurement technique for the high-time-resolution determination of equivalent organic and elemental carbon (EC) in different particulate matter size fractions, which avoids pyrolytic correction and the need for high-purity compressed gases. The performance of this online method relative to the standardized off-line thermo-optical OC–EC method and respective instruments was evaluated during a winter field campaign at an urban background location in Ljubljana, Slovenia. The organic-matter-to-organic-carbon ratio obtained from the comparison with an aerosol chemical speciation monitor (ACSM) was OM/OC=1.8, in the expected range.
Ključne besede: total carbon, aeroosl, black carbon, carbonaceous matter
Objavljeno v RUNG: 17.08.2020; Ogledov: 3051; Prenosov: 77
.pdf Celotno besedilo (226,45 KB)

69.
Chemical characterization of PM2.5 and source apportionment of organic aerosol in New Delhi, India
Anna Tobler, Deepika Bhattu, Francesco Canonaco, Vipul Lalchandani, Ashutosh Shukla, Navaneeth Thamban, Suneeti Mishra, Atul Srivastava, Deewan Bisht, Suresh Tiwari, Surender Singh, Griša Močnik, Urs Baltensperger, Sachchida Tripathi, J. G. Slowik, André S. H. Prévôt, 2020, izvirni znanstveni članek

Opis: Delhi is one of the most polluted cities worldwide and a comprehensive understanding and deeper insight into the air pollution and its sources is of high importance. We report 5 months of highly time-resolved measurements of non-refractory PM2.5 and black carbon (BC). Additionally, source apportionment based on positive matrix factorization (PMF) of the organic aerosol (OA) fraction is presented. The highest pollution levels are observed during winter in December/January. During that time, also uniquely high chloride concentrations are measured, which are sometimes even the most dominant NR-species in the morning hours. With increasing temperature, the total PM2.5 concentration decreases steadily, whereas the chloride concentrations decrease sharply. The concentrations measured in May are roughly 6 times lower than in December/January. PMF analysis resolves two primary factors, namely hydrocarbon-like (traffic-related) OA (HOA) and solid fuel combustion OA (SFC-OA), and one or two secondary factors depending on the season. The uncertainties of the PMF analysis are assessed by combining the random a-value approach and the bootstrap resampling technique of the PMF input. The uncertainties for the resolved factors range from ±18% to ±19% for HOA, ±7% to ±19% for SFC-OA and ±6 % to ±11% for the OOAs. The average correlation of HOA with eBCtr is R2 = 0.40, while SFC-OA has a correlation of R2 = 0.78 with eBCsf. Anthracene (m/z 178) and pyrene (m/z 202) (PAHs) are mostly explained by SFC-OA and follow its diurnal trend (R2 = 0.98 and R2 = 0.97). The secondary oxygenated aerosols are dominant during daytime. The average contribution during the afternoon hours (1 pm–5 pm) is 59% to the total OA mass, with contributions up to 96% in May. In contrast, the primary sources are more important during nighttime: the mean nightly contribution (22 pm–3 am) to the total OA mass is 48%, with contributions up to 88% during some episodes in April.
Ključne besede: New Delhi, PM2.5, Source apportionment, PMF
Objavljeno v RUNG: 20.07.2020; Ogledov: 2675; Prenosov: 0
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70.
A new optical-based technique for real-time measurements of mineral dust concentration in PM10 using a virtual impactor
Luka Drinovec, Jean Sciare, Iasonas Stavroulas, Spiros Bezantakos, Michael Pikridas, FLORIN UNGA, Chrysanthos Savvides, Bojana Višnjić, Maja Remškar, Griša Močnik, 2020, izvirni znanstveni članek

Opis: Atmospheric mineral dust influences Earth’s radiative budget, cloud formation, and lifetime; has adverse health effects; and affects air quality through the increase of regulatory PM10 concentrations, making its real-time quantification in the atmosphere of strategic importance. Only few near-real-time techniques can discriminate dust aerosol in PM10 samples and they are based on the dust chemical composition. The online determination of mineral dust using aerosol absorption photometers offers an interesting and competitive alternative but remains a difficult task to achieve. This is particularly challenging when dust is mixed with black carbon, which features a much higher mass absorption cross section. We build on previous work using filter photometers and present here for the first time a highly timeresolved online technique for quantification of mineral dust concentration by coupling a high-flow virtual impactor (VI) sampler that concentrates coarse particles with an aerosol absorption photometer (Aethalometer, model AE33). The absorption of concentrated dust particles is obtained by subtracting the absorption of the submicron (PM1) aerosol fraction from the absorption of the virtual impactor sample (VIPM1 method). This real-time method for detecting desert dust was tested in the field for a period of 2 months (April and May 2016) at a regional background site of Cyprus, in the Eastern Mediterranean. Several intense desert mineral dust events were observed during the field campaign with dust concentration in PM10 up to 45 μgm
Ključne besede: aerosol absorption, mineral dust, on-line detection, air quality
Objavljeno v RUNG: 20.07.2020; Ogledov: 2885; Prenosov: 0
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