61. Hidden black carbon air pollution in hilly rural areas - a case study of Dinaric depressionKristina 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: 2347; Prenosov: 0
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62. A single-beam photothermal interferometer for in situ measurements of aerosol light absorptionBradley 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: 2583; Prenosov: 74
 Celotno besedilo (2,44 MB) |
63. Performance of microAethalometers: Real-world Field Intercomparisons from Multiple Mobile Measurement Campaigns in Different Atmospheric EnvironmentsHoney 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: 2646; Prenosov: 183
Celotno besedilo (3,54 MB) |
64. Photo-thermal interferometerLuka 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: 2902; Prenosov: 0
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65. 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: 3179; Prenosov: 0
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66. The new instrument using a TC–BC (total carbon–black carbon) method for the online measurement of carbonaceous aerosolsMartin 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: 2902; Prenosov: 76
Celotno besedilo (226,45 KB) |
67. Chemical characterization of PM2.5 and source apportionment of organic aerosol in New Delhi, IndiaAnna 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: 2550; Prenosov: 0
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68. A new optical-based technique for real-time measurements of mineral dust concentration in PM10 using a virtual impactorLuka 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: 2740; Prenosov: 0
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69. Substantial brown carbon emissions from wintertime residential wood burning over FranceYunjiang Zhang, Alexandre Albinet, Jean-Eudes Petit, Véronique Jacob, Florie Chevrier, Gregory Gille, Sabrina Pontet, Eve Chrétien, Marta Dominik-Sègue, Gilles Levigoureux, Griša Močnik, Valérie Gros, Jean-Luc Jaffrezo, Olivier Favez, 2020, izvirni znanstveni članek Opis: Brown carbon (BrC) is known to absorb light at subvisible wavelengths but its optical properties and sources are still poorly documented, leading to large uncertainties in climate studies. Here, we show its major wintertime contribution to total aerosol absorption at 370 nm (18–42%) at 9 different French sites. Moreover, an excellent correlation with levoglucosan (r2 = 0.9 and slope = 22.2 at 370 nm), suggesting important contribution of wood burning emissions to ambient BrC aerosols in France. At all sites, BrC peaks were mainly observed during late evening, linking to local intense residential wood burning during this time period. Furthermore, the geographic origin analysis also highlighted the high potential contribution of local and/or small-regional emissions to BrC. Focusing on the Paris region, twice higher BrC mass absorption efficiency value was obtained for less oxidized biomass burning organic aerosols (BBOA) compared to more oxidized BBOA (e.g., about 4.9 ± 0.2 vs. 2.0 ± 0.1 m2 g−1, respectively, at 370 nm). Finally, the BBOA direct radiative effect was found to be 40% higher when these two BBOA fractions are treated as light-absorbing species, compared to the non-absorbing BBOA scenario.
Ključne besede: Brown carbon, Multi sites, Residential wood burning, Mass absorption efficiency, France
Objavljeno v RUNG: 20.07.2020; Ogledov: 3039; Prenosov: 0
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70. Comparison and complementary use of in situ and remote sensing aerosol measurements in the Athens Metropolitan AreaS. Vratolis, Griša Močnik, Konstantinos Eleftheriadis, 2020, izvirni znanstveni članek Opis: In the summer of 2014 in situ and remote sensing instruments were deployed in Athens, in order to study the concentration, physical properties, and chemical composition of aerosols. In this manuscript we aim to combine the measurements of collocated in situ and remote sensing instruments by comparison and complementary use, in order to increase the accuracy of predictions concerning climate change and human health. We also develop a new method in order to select days when a direct comparison on in situ and remote sensing instruments is possible. On selected days that displayed significant turbulence up to approximately 1000 m above ground level (agl), we acquired the aerosol extinction or scattering coefficient by in situ instruments using three approaches. In the first approach the aerosol extinction coefficient was acquired by adding a Nephelometer scattering coefficient in ambient conditions and an Aethalometer absorption coefficient. The correlation between the in situ and remote sensing instruments was good (coefficient of determination equal to 0.69). In the second approach we acquired the aerosol refractive index by fitting dry Nephelometer and Aethalometer measurements with Mie algorithm calculations of the scattering and absorption coefficients for the size distribution up to a maximum diameter of 1000 nm obtained by in situ instruments. The correlation in this case was relatively good ( equal to 0.56). Our next step was to compare the extinction coefficient acquired by remote sensing instruments to the scattering coefficient calculated by Mie algorithm using the size distribution up to a maximum diameter of 1000 nm and the equivalent refractive index (), which is acquired by the comparison of the size distributions obtained by a Scanning Mobility Particle Sizer (SMPS) and an Optical Particle Counter (OPC). The agreement between the in situ and remote sensing instruments in this case was not satisfactory ( equal to 0.35). The last comparison for the selected days was between the aerosol extinction Ångström exponent acquired by in situ and remote sensing instruments. The correlation was not satisfactory ( equal to 0.4), probably due to differences in the number size distributions present in the air volumes measured by in situ and remote sensing instruments. We also present a day that a Saharan dust event occurred in Athens in order to demonstrate the information we obtain through the synergy of in situ and remote sensing instruments on how regional aerosol is added to local aerosol, especially during pollution events due to long range transport.
Ključne besede: Aerosol mixing in the vertical, In situ — Remote sensing comparison, Regional aerosol addition to local aerosol
Objavljeno v RUNG: 09.04.2020; Ogledov: 2913; Prenosov: 0
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