31. |
32. Equal abundance of summertime natural and wintertime anthropogenic Arctic organic aerosolsVaios Moschos, Katja Dzepina, Deepika Bhattu, Houssni Lamkaddam, Roberto Casotto, Kaspar R. Daellenbach, Francesco Canonaco, Pragati Rai, Wenche Aas, Silvia Becagli, Giulia Calzolai, Konstantinos Eleftheriadis, Claire E. Moffett, Jürgen Schnelle-Kreis, Mirko Severi, Sangeeta Sharma, Henrik Skov, Mika Vestenius, Wendy Zhang, Hannele Hakola, Heidi Hellén, Lin Huang, Jean-Luc Jaffrezo, Andreas Massling, Jakob K. Nøjgaard, Tuuka Petäjä, Olga Popovicheva, Rebecca J. Sheesley, Rita Traversi, Karl Espen Yttri, Julia Schmale, André S. H. Prévôt, Urs Baltensperger, Imad El Haddad, 2022, original scientific article Abstract: Aerosols play an important yet uncertain role in modulating the radiation balance of the sensitive Arctic atmosphere. Organic aerosol is one of the most abundant, yet least understood, fractions of the Arctic aerosol mass. Here we use data from eight observatories that represent the entire Arctic to reveal the annual cycles in anthropogenic and biogenic sources of organic aerosol. We show that during winter, the organic aerosol in the Arctic is dominated by anthropogenic emissions, mainly from Eurasia, which consist of both direct combustion emissions and long-range transported, aged pollution. In summer, the decreasing anthropogenic pollution is replaced by natural emissions. These include marine secondary, biogenic secondary and primary biological emissions, which have the potential to be important to Arctic climate by modifying the cloud condensation nuclei properties and acting as ice-nucleating particles. Their source strength or atmospheric processing is sensitive to nutrient availability, solar radiation, temperature and snow cover. Our results provide a comprehensive understanding of the current pan-Arctic organic aerosol, which can be used to support modelling efforts that aim to quantify the climate impacts of emissions in this sensitive region.
Keywords: Arctic, Organic aerosols, Emission sources, Climate change
Published in RUNG: 01.03.2022; Views: 1544; Downloads: 0
This document has many files! More... |
33. Comparing black-carbon- and aerosol-absorption-measuring instruments – a new system using lab-generated soot coated with controlled amounts of secondary organic matterDaniel M. Kalbermatter, Griša Močnik, Luka Drinovec, Bradley Visser, Jannis Röhrbein, Matthias Oscity, Ernest Weingartner, Antti-Pekka Hyvärinen, Konstantina Vasilatou, 2022, original scientific article Abstract: We report on an inter-comparison of black-carbon- and aerosol-absorption-measuring instruments with laboratory-generated soot particles coated with controlled amounts of secondary organic matter (SOM). The aerosol generation setup consisted of a miniCAST 5201 Type BC burner for the generation of soot particles and a new automated oxidation flow reactor based on the micro smog chamber (MSC) for the generation of SOM from the ozonolysis of α-pinene. A series of test aerosols was generated with elemental to total carbon (EC TC) mass fraction ranging from about 90 % down to 10 % and single-scattering albedo (SSA at 637 nm) from almost 0 to about 0.7. A dual-spot Aethalometer AE33, a photoacoustic extinctiometer (PAX, 870 nm), a multi-angle absorption photometer (MAAP), a prototype photoacoustic instrument, and two prototype photo-thermal interferometers (PTAAM-2λ and MSPTI) were exposed to the test aerosols in parallel. Significant deviations in the response of the instruments were observed depending on the amount of secondary organic coating. We believe that the setup and methodology described in this study can easily be standardised and provide a straightforward and reproducible procedure for the inter-comparison and characterisation of both filter-based and in situ black-carbon-measuring (BC-measuring) instruments based on realistic test aerosols.
Keywords: black carbon, aerosol absorption, secondary organic aerosol, coating
Published in RUNG: 01.02.2022; Views: 1663; Downloads: 48
 Full text (752,94 KB) |
34. Characterization of non-refractory (NR) PM[sub]1 and source apportionment of organic aerosol in Kraków, PolandAnna Tobler, Alicja Skiba, Francesco Canonaco, Griša Močnik, Pragati Rai, Gang Chen, Jakub Bartyzel, Miroslaw Zimnoch, Katarzyna Styszko, Jaroslaw Nęcki, 2021, original scientific article Abstract: Kraków is routinely affected by very high air pollution levels, especially during the winter months. Although a lot of effort has been made to characterize ambient aerosol, there is a lack of online and long-term measurements of non-refractory aerosol. Our measurements at the AGH University of Science and Technology provide the online long-term chemical composition of ambient submicron particulate matter (PM1) between January 2018 and April 2019. Here we report the chemical characterization of non-refractory submicron aerosol and source apportionment of the organic fraction by positive matrix factorization (PMF). In contrast to other long-term source apportionment studies, we let a small PMF window roll over the dataset instead of performing PMF over the full dataset or on separate seasons. In this way, the seasonal variation in the source profiles can be captured. The uncertainties in the PMF solutions are addressed by the bootstrap resampling strategy and the random a-value approach for constrained factors.
We observe clear seasonal patterns in the concentration and composition of PM1, with high concentrations during the winter months and lower concentrations during the summer months. Organics are the dominant species throughout the campaign. Five organic aerosol (OA) factors are resolved, of which three are of a primary nature (hydrocarbon-like OA (HOA), biomass burning OA (BBOA) and coal combustion OA (CCOA)) and two are of a secondary nature (more oxidized oxygenated OA (MO-OOA) and less oxidized oxygenated OA (LO-OOA)). While HOA contributes on average 8.6 % ± 2.3 % throughout the campaign, the solid-fuel-combustion-related BBOA and CCOA show a clear seasonal trend with average contributions of 10.4 % ± 2.7 % and 14.1 %, ±2.1 %, respectively. Not only BBOA but also CCOA is associated with residential heating because of the pronounced yearly cycle where the highest contributions are observed during wintertime. Throughout the campaign, the OOA can be separated into MO-OOA and LO-OOA with average contributions of 38.4 % ± 8.4 % and 28.5 % ± 11.2 %, respectively.
Keywords: air pollution, PM1, organic aerosol, black carbon, source apportionment, PMF
Published in RUNG: 08.10.2021; Views: 1848; Downloads: 0
This document has many files! More... |
35. Charge transport characterization of P3HT thin-film organic semiconductor : Written report: in fulfilment of diploma seminar 1FAF29 requirementMatija Filipčič, 2021, research project (high school) Abstract: The focus of this diploma seminar is to describe different types of charge transport theory and
models used for finding mobility in semiconductors, more specifically focused on P3HT thin-film
organic semiconductor. It also describes the time-of-flight method, which was used to measure the
experimental data for P3HT with time dependent current I(t) curve. Another data set was obtained
by performing Kinetic Monte Carlo (KMC) simulations using Miller-Abrahams hopping formalism.
KMC was used to determine the material disorder, simulate I(t) curve and transit time for every
charge carrier. Simulated data, different transit times and mobilities were then finally compared
with experimental, in order to find agreements between the two.
Keywords: charge transport, P3HT, thin-film organic semiconductor
Published in RUNG: 15.09.2021; Views: 2240; Downloads: 0
This document has many files! More... |
36. Untargeted molecular analysis of exhaled breath as a diagnostic test for ventilator-associated lower respiratory tract infections (BreathDx)Pouline M. van Oort, Tamara M. E. Nijsen, Iain R. White, Hugo Knobel, Timothy Felton, Nicholas J. W. Rattray, Oluwasola Lawal, Murtaza Bulut, Waqar Ahmed, Antonio Artigas, 2021, short scientific article Abstract: Patients suspected of ventilator-associated lower respiratory tract infections (VA-LRTIs) commonly receive broad-spectrum antimicrobial therapy unnecessarily. We tested whether exhaled breath analysis can discriminate between patients suspected of VA-LRTI with confirmed infection, from patients with negative cultures. Breath from 108 patients suspected of VA-LRTI was analysed by gas chromatography-mass spectrometry. The breath test had a sensitivity of 98% at a specificity of 49%, confirmed with a second analytical method. The breath test had a negative predictive value of 96% and excluded pneumonia in half of the patients with negative cultures. Trial registration number: UKCRN ID number 19086, registered May 2015.
Keywords: ventilator-associated pneumonia, breath analysis, volatile organic compounds, metabolomics, intensive care, hospital acquired infections
Published in RUNG: 07.09.2021; Views: 4125; Downloads: 0
This document has many files! More... |
37. Electrochemical ZnO-based impedimetric sensor for aqueous ammonia detection for precision animal agricultureKateryna Vyshniakova, Huiwen Bai, Victor Marco Rocha Malacco, Egon Pavlica, Richard M. Voyles, Shawn S. Donkin, Amanda Gehman, Robert A. Nawrocki, 2021, published scientific conference contribution abstract Keywords: electrochemical impedance spectroscopy, mixed conduction, organic sensor
Published in RUNG: 07.06.2021; Views: 2050; Downloads: 37
 Link to full text
This document has many files! More... |
38. Covalent Organic Polymers and Frameworks for Fluorescence-Based SensorsTina Škorjanc, Dinesh Shetty, Matjaž Valant, 2021, review article Keywords: fluorescence, sensors, covalent organic polymers, covalent organic frameworks, quenching, ions, explosives
Published in RUNG: 05.05.2021; Views: 2219; Downloads: 221
Link to full text
This document has many files! More... |
39. Sources and transformations of particle-bound polycyclic aromatic hydrocarbons in Mexico CityL. 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, original scientific article Abstract: 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.
Keywords: aerosol mass-spectrometer, aerodynamic diameter measurements, oxygenated organic aerosols, relative rate constants
Published in RUNG: 12.04.2021; Views: 2167; Downloads: 0
This document has many files! More... |
40. Secondary organic aerosol formation from anthropogenic air pollution : rapid and higher than expectedRainer Volkamer, Jose L. Jimenez, F. M. San Martini, Katja Džepina, Q. Zhang, Dara Salcedo, Luisa T. Molina, D. Worsnop, 2006, original scientific article Abstract: 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.
Keywords: atmospheric aerosol, atmospheric chemistry, volatile organic compounds, secondary organic aerosols
Published in RUNG: 12.04.2021; Views: 2974; Downloads: 0
This document has many files! More... |
