Articles | Volume 19, issue 12
https://doi.org/10.5194/amt-19-4035-2026
© Author(s) 2026. This work is distributed under
the Creative Commons Attribution 4.0 License.
the Creative Commons Attribution 4.0 License.
https://doi.org/10.5194/amt-19-4035-2026
© Author(s) 2026. This work is distributed under
the Creative Commons Attribution 4.0 License.
the Creative Commons Attribution 4.0 License.
Sodium thiosulfate-coated ceramic denuders for ozone removal in ultrafine particle sampling
Elisabeth Eckenberger
CORRESPONDING AUTHOR
Bayreuth Center of Ecology and Environmental Research (BayCEER), University of Bayreuth, Bayreuth, Germany
Andreas Mittereder
Department of Engineering Thermodynamics and Transport Processes, University of Bayreuth, Bayreuth, Germany
Nadine Gawlitta
Joint Mass Spectrometry Centre (JMSC) at Comprehensive Molecular Analytics, Helmholtz Zentrum München, Neuherberg, Germany
JMSC at Chair of Analytical Chemistry, Institute of Chemistry, University of Rostock, Rostock, Germany
Martin Sklorz
Joint Mass Spectrometry Centre (JMSC) at Comprehensive Molecular Analytics, Helmholtz Zentrum München, Neuherberg, Germany
JMSC at Chair of Analytical Chemistry, Institute of Chemistry, University of Rostock, Rostock, Germany
Dieter Brüggemann
Department of Engineering Thermodynamics and Transport Processes, University of Bayreuth, Bayreuth, Germany
Ralf Zimmermann
Joint Mass Spectrometry Centre (JMSC) at Comprehensive Molecular Analytics, Helmholtz Zentrum München, Neuherberg, Germany
JMSC at Chair of Analytical Chemistry, Institute of Chemistry, University of Rostock, Rostock, Germany
Anke Christine Nölscher
CORRESPONDING AUTHOR
Bayreuth Center of Ecology and Environmental Research (BayCEER), University of Bayreuth, Bayreuth, Germany
now at: Institute of Climate and Energy Systems – Troposphere (ICE-3), Forschungszentrum Jülich GmbH, Jülich, Germany
now at: Institute of Geophysics and Meteorology, University of Cologne, Cologne, Germany
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Elisabeth Eckenberger, Andreas Mittereder, Nadine Gawlitta, Jürgen Schnelle-Kreis, Martin Sklorz, Dieter Brüggemann, Ralf Zimmermann, and Anke C. Nölscher
Aerosol Research, 3, 45–64, https://doi.org/10.5194/ar-3-45-2025, https://doi.org/10.5194/ar-3-45-2025, 2025
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We assessed the performance of four cascade impactors for collecting and analyzing organic markers in airborne ultrafine particles (UFPs) under lab and field conditions. The cutoff was influenced by the impactor design and aerosol mixture. Two key factors caused variations in mass concentrations: the evaporation of semi-volatile compounds and the "bounce-off" of larger particles and fragments. Our findings reveal the challenges of analyzing organic marker mass concentrations in airborne UFPs.
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This preprint is open for discussion and under review for Atmospheric Chemistry and Physics (ACP).
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The dynamics of how tire wear particles behaves prior to their entrainment are still poorly understood. In wind tunnel experiments, these particle detachment from an idealised glass substrate were monitored. For particle size above 80 μm, smaller and more rounded particles were mobilised by wind shear first, whereas larger and more angular particles require stronger wind shear, highlighting strong surface adhesion and particle morphology as the major factors influencing microplastic detachment.
Anni Hartikainen, Mika Ihalainen, Deeksha Shukla, Marius Rohkamp, Arya Mukherjee, Quanfu He, Sandra Piel, Aki Virkkula, Delun Li, Tuukka Kokkola, Seongho Jeong, Hanna Koponen, Uwe Etzien, Anusmita Das, Krista Luoma, Lukas Schwalb, Thomas Gröger, Alexandre Barth, Martin Sklorz, Thorsten Streibel, Hendryk Czech, Benedikt Gündling, Markus Kalberer, Bert Buchholz, Andreas Hupfer, Thomas Adam, Thorsten Hohaus, Johan Øvrevik, Ralf Zimmermann, and Olli Sippula
Atmos. Chem. Phys., 25, 9275–9294, https://doi.org/10.5194/acp-25-9275-2025, https://doi.org/10.5194/acp-25-9275-2025, 2025
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Marco Schmidt, Haseeb Hakkim, Lukas Anders, Aleksandrs Kalamašņikovs, Thomas Kröger-Badge, Robert Irsig, Norbert Graf, Reinhard Kelnberger, Johannes Passig, and Ralf Zimmermann
Atmos. Meas. Tech., 18, 2425–2437, https://doi.org/10.5194/amt-18-2425-2025, https://doi.org/10.5194/amt-18-2425-2025, 2025
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Laser desorption of individual particles prior to ionization is the key to reveal their organic composition. The CO2 lasers required are bulky and maintenance-intensive, limiting their use in the field. We have developed a compact solid-state IR laser that is easily aligned with the particle beam. Mass spectra and hit rates are similar to those of the CO2 laser. For combined characterization of organic and inorganic particle compositions, both lasers are superior to conventional single UV pulses.
Battist Utinger, Alexandre Barth, Andreas Paul, Arya Mukherjee, Steven John Campbell, Christa-Maria Müller, Mika Ihalainen, Pasi Yli-Pirilä, Miika Kortelainen, Zheng Fang, Patrick Martens, Markus Somero, Juho Louhisalmi, Thorsten Hohaus, Hendryk Czech, Olli Sippula, Yinon Rudich, Ralf Zimmermann, and Markus Kalberer
Aerosol Research, 3, 205–218, https://doi.org/10.5194/ar-3-205-2025, https://doi.org/10.5194/ar-3-205-2025, 2025
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The oxidative potential (OP) of air pollution particles might be a metric explaining particle toxicity. This study quantifies the OP of fresh and aged car and wood burning emission particles and explores how the OP changes over time, using novel high-temporal-resolution instruments. We show that emissions from wood burning are more toxic than car exhaust per unit particle mass, especially as they age in the atmosphere. We also calculate emission factors for the OP, which could help to improve air pollution policies.
Elisabeth Eckenberger, Andreas Mittereder, Nadine Gawlitta, Jürgen Schnelle-Kreis, Martin Sklorz, Dieter Brüggemann, Ralf Zimmermann, and Anke C. Nölscher
Aerosol Research, 3, 45–64, https://doi.org/10.5194/ar-3-45-2025, https://doi.org/10.5194/ar-3-45-2025, 2025
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We assessed the performance of four cascade impactors for collecting and analyzing organic markers in airborne ultrafine particles (UFPs) under lab and field conditions. The cutoff was influenced by the impactor design and aerosol mixture. Two key factors caused variations in mass concentrations: the evaporation of semi-volatile compounds and the "bounce-off" of larger particles and fragments. Our findings reveal the challenges of analyzing organic marker mass concentrations in airborne UFPs.
Luiz A. T. Machado, Jürgen Kesselmeier, Santiago Botía, Hella van Asperen, Meinrat O. Andreae, Alessandro C. de Araújo, Paulo Artaxo, Achim Edtbauer, Rosaria R. Ferreira, Marco A. Franco, Hartwig Harder, Sam P. Jones, Cléo Q. Dias-Júnior, Guido G. Haytzmann, Carlos A. Quesada, Shujiro Komiya, Jost Lavric, Jos Lelieveld, Ingeborg Levin, Anke Nölscher, Eva Pfannerstill, Mira L. Pöhlker, Ulrich Pöschl, Akima Ringsdorf, Luciana Rizzo, Ana M. Yáñez-Serrano, Susan Trumbore, Wanda I. D. Valenti, Jordi Vila-Guerau de Arellano, David Walter, Jonathan Williams, Stefan Wolff, and Christopher Pöhlker
Atmos. Chem. Phys., 24, 8893–8910, https://doi.org/10.5194/acp-24-8893-2024, https://doi.org/10.5194/acp-24-8893-2024, 2024
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Composite analysis of gas concentration before and after rainfall, during the day and night, gives insight into the complex relationship between trace gas variability and precipitation. The analysis helps us to understand the sources and sinks of trace gases within a forest ecosystem. It elucidates processes that are not discernible under undisturbed conditions and contributes to a deeper understanding of the trace gas life cycle and its intricate interactions with cloud dynamics in the Amazon.
Finja Löher, Esther Borrás, Amalia Muñoz, and Anke Christine Nölscher
Atmos. Meas. Tech., 17, 4553–4579, https://doi.org/10.5194/amt-17-4553-2024, https://doi.org/10.5194/amt-17-4553-2024, 2024
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We constructed and characterized a new indoor Teflon atmospheric simulation chamber. We evaluated wall losses, photolysis rates, and secondary reactions of multifunctional photooxidation products in the chamber. To measure these products on-line, we combined chromatographic and mass spectrometric analyses to obtain both isomeric information and a high temporal resolution. For method validation, we studied the formation yields of the main ring-retaining products of toluene.
Eric Schneider, Hendryk Czech, Olga Popovicheva, Marina Chichaeva, Vasily Kobelev, Nikolay Kasimov, Tatiana Minkina, Christopher Paul Rüger, and Ralf Zimmermann
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This study provides insights into the complex chemical composition of long-range-transported wildfire plumes from Yakutia, which underwent different levels of atmospheric processing. With complementary mass spectrometric techniques, we improve our understanding of the chemical processes and atmospheric fate of wildfire plumes. Unprecedented high levels of carbonaceous aerosols crossed the polar circle with implications for the Arctic ecosystem and consequently climate.
Julius Seidler, Markus N. Friedrich, Christoph K. Thomas, and Anke C. Nölscher
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Here, we study the transport of ultrafine particles (UFPs) from an airport to two new adjacent measuring sites for 1 year. The number of UFPs in the air and the diurnal variation are typical urban. Winds from the airport show increased number concentrations. Additionally, considering wind frequencies, we estimate that, from all UFPs measured at the two sites, 10 %–14 % originate from the airport and/or other UFP sources from between the airport and site.
Johannes Passig, Julian Schade, Robert Irsig, Thomas Kröger-Badge, Hendryk Czech, Thomas Adam, Henrik Fallgren, Jana Moldanova, Martin Sklorz, Thorsten Streibel, and Ralf Zimmermann
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The single-particle distribution of health-relevant polycyclic aromatic hydrocarbons (PAHs) was studied at the Swedish coast in autumn. We found PAHs bound to long-range transported particles from eastern and central Europe and also from ship emissions and local sources. This is the first field study using a new technology revealing single-particle data from both inorganic components and PAHs. We discuss PAH profiles that are indicative of several sources and atmospheric aging processes.
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Short summary
Ozone in sampling air can alter the chemical composition of collected ultrafine particles, leading to an inaccurate air quality assessment. We addressed this by developing a ceramic device coated with sodium thiosulfate that eliminates ozone before it reaches the filter. Our results show this tool effectively preserves ozone-sensitive components, such as polycyclic aromatic hydrocarbons, without particle losses. This contributes to more reliable data for air quality research.
Ozone in sampling air can alter the chemical composition of collected ultrafine particles,...