Auflistung nach Autor:in "Peter, Thomas"

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  • Vorschaubild
    Publikation
    A combined particle trap/HTDMA hygroscopicity study of mixed inorganic/organic aerosol particles
    (Copernicus, 19.09.2008) Zardini, Alessandro A.; Sjogren, S.; Marcolli, Claudia; Krieger, Ulrich K.; Gysel, Martin; Weingartner, Ernest; Baltensperger, Urs; Peter, Thomas [in: Atmospheric Chemistry and Physics]
    Atmospheric aerosols are often mixtures of inorganic and organic material. Organics can represent a large fraction of the total aerosol mass and are comprised of water-soluble and insoluble compounds. Increasing attention was paid in the last decade to the capability of mixed inorganic/organic aerosol particles to take up water (hygroscopicity). We performed hygroscopicity measurements of internally mixed particles containing ammonium sulfate and carboxylic acids (citric, glutaric, adipic acid) in parallel with an electrodynamic balance (EDB) and a hygroscopicity tandem differential mobility analyzer (HTDMA). The organic compounds were chosen to represent three distinct physical states. During hygroscopicity cycles covering hydration and dehydration measured by the EDB and the HTDMA, pure citric acid remained always liquid, adipic acid remained always solid, while glutaric acid could be either. We show that the hygroscopicity of mixtures of the above compounds is well described by the Zdanovskii-Stokes-Robinson (ZSR) relationship as long as the two-component particle is completely liquid in the ammonium sulfate/glutaric acid system; deviations up to 10% in mass growth factor (corresponding to deviations up to 3.5% in size growth factor) are observed for the ammonium sulfate/citric acid 1:1 mixture at 80% RH. We observe even more significant discrepancies compared to what is expected from bulk thermodynamics when a solid component is present. We explain this in terms of a complex morphology resulting from the crystallization process leading to veins, pores, and grain boundaries which allow for water sorption in excess of bulk thermodynamic predictions caused by the inverse Kelvin effect on concave surfaces.
    01A - Beitrag in wissenschaftlicher Zeitschrift
  • Vorschaubild
    Publikation
    Ground-based and airborne in-situ measurements of the Eyjafjallajökull volcanic aerosol plume in Switzerland in spring 2010
    (Copernicus, 04.10.2011) Bukowiecki, Nicolas; Zieger, Paul; Weingartner, Ernest; Jurányi, Zsófia; Gysel, Martin; Neininger, Bruno; Schneider, Boris; Hueglin, Christoph; Ulrich, Andrea; Wichser, Adrian; Henne, Stephan; Brunner, Dominik; Kaegi, Ralf; Schwikowski, Margit; Tobler, Leonhard; Wienhold, Frank G.; Engel, Ilana; Buchmann, Brigitte; Peter, Thomas; Baltensperger, Urs [in: Atmospheric Chemistry and Physics]
    The volcanic aerosol plume resulting from the Eyjafjallajökull eruption in Iceland in April and May 2010 was detected in clear layers above Switzerland during two periods (17–19 April 2010 and 16–19 May 2010). In-situ measurements of the airborne volcanic plume were performed both within ground-based monitoring networks and with a research aircraft up to an altitude of 6000 m a.s.l. The wide range of aerosol and gas phase parameters studied at the high altitude research station Jungfraujoch (3580 m a.s.l.) allowed for an in-depth characterization of the detected volcanic aerosol. Both the data from the Jungfraujoch and the aircraft vertical profiles showed a consistent volcanic ash mode in the aerosol volume size distribution with a mean optical diameter around 3 ± 0.3 μm. These particles were found to have an average chemical composition very similar to the trachyandesite-like composition of rock samples collected near the volcano. Furthermore, chemical processing of volcanic sulfur dioxide into sulfate clearly contributed to the accumulation mode of the aerosol at the Jungfraujoch. The combination of these in-situ data and plume dispersion modeling results showed that a significant portion of the first volcanic aerosol plume reaching Switzerland on 17 April 2010 did not reach the Jungfraujoch directly, but was first dispersed and diluted in the planetary boundary layer. The maximum PM10 mass concentrations at the Jungfraujoch reached 30 μgm−3 and 70 μgm−3 (for 10-min mean values) duri ng the April and May episode, respectively. Even low-altitude monitoring stations registered up to 45 μgm−3 of volcanic ash related PM10 (Basel, Northwestern Switzerland, 18/19 April 2010). The flights with the research aircraft on 17 April 2010 showed one order of magnitude higher number concentrations over the northern Swiss plateau compared to the Jungfraujoch, and a mass concentration of 320 (200–520) μgm−3 on 18 May 2010 over the northwestern Swiss plateau. The presented data significantly contributed to the time-critical assessment of the local ash layer properties during the initial eruption phase. Furthermore, dispersion models benefited from the detailed information on the volcanic aerosol size distribution and its chemical composition.
    01A - Beitrag in wissenschaftlicher Zeitschrift
  • Vorschaubild nicht verfügbar
    Publikation
    Hygroscopic growth and water uptake kinetics of two-phase aerosol particles consisting of ammonium sulfate, adipic and humic acid mixtures
    (Elsevier, 02/2007) Sjögren, Staffan; Gysel, Martin; Weingartner, Ernest; Baltensperger, Urs; Cubison, Michael J.; Coe, Hugh; Zardini, Alessandro A.; Marcolli, Claudia; Krieger, Ulrich K.; Peter, Thomas [in: Journal of Aerosol Science]
    The hygroscopic growth of solid aerosol particles consisting of mixtures of ammonium sulfate and either adipic acid or Aldrich humic acid sodium salt was characterized with a hygroscopicity tandem differential mobility analyzer and an electrodynamic balance. In particular, the time required for the aerosol particle phase and the surrounding water vapor to reach equilibrium at high relative humidity (RH) was investigated. Depending on the chemical composition of the particles, residence times of > 40 s were required to reach equilibrium at 85% RH, yielding up to a 7% reduction in the measured hygroscopic growth factors from measurements at 4 s residence time compared to measurements at equilibrium. We suggest that the solid organic compound, when present as the dominant component, encloses the water-soluble inorganic salt in veins and cavities, resulting in the observed slow water uptake. Comparison with predictions from the Zdanovskii-Stokes-Robinson relation shows enhanced water uptake of the mixed particles. This is explained with the presence of the salt solution in veins resulting in a negative curvature of the solution meniscus at the opening of the vein. In conclusion, it is important for studies of mixtures of water soluble compounds with insoluble material to allow for sufficient residence time at the specified humidity to reach equilibrium before the hygroscopicity measurements.
    01A - Beitrag in wissenschaftlicher Zeitschrift
  • Vorschaubild
    Publikation
    Spatial variation of aerosol optical properties around the high-alpine site Jungfraujoch (3580 m a.s.l.)
    (Copernicus, 08.08.2012) Zieger, Paul; Kienast-Sjögren, Erika; Starace, Michela; von Bismarck, Jonas; Bukowiecki, Nicolas; Baltensperger, Urs; Wienhold, Frank Gunther; Peter, Thomas; Ruhtz, Thomas; Collaud Coen, Martine; Vuilleumier, Laurent; Maier, Olaf; Emili, Emanuele; Popp, Christian; Weingartner, Ernest [in: Atmospheric Chemistry and Physics]
    This paper presents results of the extensive field campaign CLACE 2010 (Cloud and Aerosol Characterization Experiment) performed in summer 2010 at the Jungfraujoch (JFJ) and the Kleine Scheidegg (KLS) in the Swiss Alps. The main goal of this campaign was to investigate the vertical variability of aerosol optical properties around the JFJ and to show the consistency of the different employed measurement techniques considering explicitly the effects of relative humidity (RH) on the aerosol light scattering. Various aerosol optical and microphysical parameters were recorded using in-situ and remote sensing techniques. In-situ measurements of aerosol size distribution, light scattering, light absorption and scattering enhancement due to water uptake were performed at the JFJ at 3580 m a.s.l.. A unique set-up allowed remote sensing measurements of aerosol columnar and vertical properties from the KLS located about 1500 m below and within the line of sight to the JFJ (horizontal distance of approx. 4.5 km). In addition, two satellite retrievals from the Spinning Enhanced Visible and Infrared Imager (SEVIRI) and the Moderate Resolution Imaging Spectroradiometer (MODIS) as well as back trajectory analyses were added to the comparison to account for a wider geographical context. All in-situ and remote sensing measurements were in clear correspondence. The ambient extinction coefficient measured in situ at the JFJ agreed well with the KLS-based LIDAR (Light Detection and Ranging) retrieval at the altitude-level of the JFJ under plausible assumptions on the LIDAR ratio. However, we can show that the quality of this comparison is affected by orographic effects due to the exposed location of the JFJ on a saddle between two mountains and next to a large glacier. The local RH around the JFJ was often higher than in the optical path of the LIDAR measurement, especially when the wind originated from the south via the glacier, leading to orographic clouds which remained lower than the LIDAR beam. Furthermore, the dominance of long-range transported Saharan dust was observed in all easurements for several days, however only for a shorter time period in the in-situ measurements due to the vertical structure of the dust plume. The optical properties of the aerosol column retrieved from SEVIRI and MODIS showed the same magnitude and a similar temporal evolution as the measurements at the KLS and the JFJ. Remaining differences are attributed to the complex terrain and simplifications in the aerosol retrieval scheme in general.
    01A - Beitrag in wissenschaftlicher Zeitschrift