Name of research institute or organization: Technische Universität Darmstadt, Institut für Angewandte Geowissenschaften, Umweltmineralogie

Similar documents
Name of research institute or organization: Technische Universität Darmstadt, Institut für Angewandte Geowissenschaften, Umweltmineralogie

Name of research institute or organization: Technische Universität Darmstadt, Institut für Angewandte Geowissenschaften, Umweltmineralogie

ARTICLE IN PRESS. Received 18 December 2006; received in revised form 14 June 2007; accepted 21 June 2007

Inadvertent climate modification due to anthropogenic lead

THE VARIABILITY OF ICE NUCLEATING AEROSOLS OVER CENTRAL EUROPE

GAW - WCCAP recommendation for aerosol inlets and sampling tubes

Changes in the manuscript are highlighted as follows: Referee#1 yellow Referee#2 green Referee#3 red Additional changes blue.

Characterisation of atmospheric aerosol sampled from an aircraft using scanning electron microscopy

Quantification of Icelandic dust export: proposal of a combined measurement and modeling experiment

Chapter Eight: Conclusions and Future Work

Airborne aerosol in-situ observations of volcanic ash layers of the Eyjafjallajökull volcano in April & May, 2010, over central Europe

Characterization of residuals from ice particles and droplets sampled in tropical deep convective cloud systems during ACRIDICON-CHUVA

Separating Cloud Forming Nuclei from Interstitial Aerosol

Insights Into Atmospheric Organic Aerosols Using An Aerosol Mass Spectrometer

Characterization and first results of an ice nucleating particle measurement system based on counterflow virtual impactor technique

Scanning Electron Microscopy

An interactive method to predict warm conveyor belt occurrence for aircraft-based field campaigns

AEROSOL-CLOUD INTERACTIONS AND PRECIPITATION IN A GLOBAL SCALE. SAHEL Conference April 2007 CILSS Ouagadougou, Burkina Faso

Black carbon enrichment in atmospheric ice particle residuals observed in lower tropospheric mixed phase clouds

Frank Drewnick & Johannes Schneider & Silke S. Hings & Nele Hock & Kevin Noone & Admir Targino & Silke Weimer & Stephan Borrmann

Atmospheric New Particle Formation and Climate Sensitivity: the CLOUD experiment.

Aerosol Dynamics. Antti Lauri NetFAM Summer School Zelenogorsk, 9 July 2008

In-situ observations of aerosol particles remaining from evaporated cirrus crystals: Comparing clean and polluted air masses

Prediction of cirrus clouds in GCMs

Klimaänderung. Robert Sausen Deutsches Zentrum für Luft- und Raumfahrt Institut für Physik der Atmosphäre Oberpfaffenhofen

IARA - GoAmazon 2014

Aircraft Icing Icing Physics

Ammonium Bisulfate/Water Equilibrium and Metastability Phase Diagrams

Direct radiative forcing due to aerosols in Asia during March 2002

Supporting Information

Detection of young contrails selected results from the CONCERT (CONtrail and Cirrus ExpeRimenT) campaign

J. Schneider & Chr. Voigt - Physics and Chemistry of Aerosols and Ice Clouds

Observations of ice nuclei and heterogeneous freezing in a Western Pacific extratropical storm

climate change Contents CO 2 (ppm)

Arctic Chemistry And Climate

Air Monitoring. Semi-continuous determination of ambient air quality

Size Distribution and Hygroscopic Properties of Agricultural Aerosols

Single-particle characterization of the Antarctic aerosols collected at King George Island, Chile

Implications of Sulfate Aerosols on Clouds, Precipitation and Hydrological Cycle

Contrail cirrus and their climate impact

Name of research institute or organization: University of Manchester, Centre for Atmospheric Science

Effects of arctic sulphuric acid aerosols on wintertime low-level atmospheric ice crystals, humidity and temperature at Alert, Nunavut

Aerosol, Cloud, Precipitation, and Radiation Interactions and Dynamics of Convective Cloud Systems (ACRIDICON)

Proposal for a Virtual Institute investigating the

A NOVEL RADIOSONDE PAYLOAD TO STUDY UPPER TROPOSPHERIC / LOWER STRATOSPHERIC AEROSOL AND CLOUDS

Atmospheric ice nuclei concentrations and characteristics constraining the role of biological ice nuclei

Ice Nucleating Particle (INP) Measurements at YMC: ETH - PINC and HINC

Name of research institute or organization: Laboratory of Atmospheric Chemistry, Paul Scherrer Institut, CH-5232 Villigen PSI, Switzerland

Irradiation of Living Cells with Single Ions at the Ion Microprobe SNAKE

Characterizing the role of diabatic processes for the modification of mid-latitude Rossby waves and Jetstream winds

The reviewer s comments are presented in italics, followed by our responses. We thank the reviewer for his comments.

Aerosol Composition and Radiative Properties

Aerosol Effects on Water and Ice Clouds

Short Course Challenges in Understanding Cloud and Precipitation Processes and Their Impact on Weather and Climate

CHAPTER 8. AEROSOLS 8.1 SOURCES AND SINKS OF AEROSOLS

Vienna Doctoral School in Physics

NOTES AND CORRESPONDENCE. High Aitken Nucleus Concentrations above Cloud Tops in the Arctic

Different Methods of Monitoring PM

Characterisation of Nanoparticle Structure by High Resolution Electron Microscopy

An investigation into the aerosol dispersion effect through the activation process in marine stratus clouds

Cloud Condensation Nuclei Hygroscopic Parameter Kappa

Chapter 7 Precipitation Processes

Precipitation Processes METR σ is the surface tension, ρ l is the water density, R v is the Gas constant for water vapor, T is the air

New Insights into Aerosol Asymmetry Parameter

Supplementary information

Dr. Laurent Vuilleumier, project leader Dr. Stephan Nyeki, Armand Vernez, Serge Brönnimann, Dr. Alain Heimo

Gas, Cloudwater, and Rain Hydrogen Peroxide and Methylhydroperoxide Measurements in RICO

Microstructure evolution during BaTiO 3 formation by solid-state reactions on rutile single crystal surfaces

Cloud scavenging of anthropogenic refractory particles at a mountain site in North China Reply to Referee#1:

Effect of aging on cloud nucleating properties of atmospheric aerosols

Spectrum of Radiation. Importance of Radiation Transfer. Radiation Intensity and Wavelength. Lecture 3: Atmospheric Radiative Transfer and Climate

ESTIMATED DESERT-DUST ICE NUCLEI

Lecture 3: Atmospheric Radiative Transfer and Climate

Influence of Organic-Containing Aerosols on Marine Boundary Layer Processes

MATRAG Measurement of Alpine Tropospheric Delay by Radiometer and GPS

Relationships of Biomass-Burning Aerosols to Ice in Orographic Wave Clouds

LABORATORY 5 AEROSOL AND CLOUD PARTICLE CHEMICAL COMPOSITION. by Dr. Randy Borys Desert Research Institute Reno, NV

Twenty years of experiments with the "M-55 Geophysica" on aerosols and clouds in the UTLS: results, discussions, controversies

A Possible Role for Immersion Freezing in Mixed-phase Stratus Clouds. Gijs de Boer T. Hashino, G.J. Tripoli, and E.W. Eloranta

Mystery of ice multiplication in warm based precipitating shallow cumulus clouds

Chemical characteristics of ice residual nuclei in anvil cirrus clouds: evidence for homogeneous and heterogeneous ice formation

Aerosols AP sizes AP types Sources Sinks Amount and lifetime Aerosol radiative effects. Aerosols. Trude Storelvmo Aerosols 1 / 21

European ceilometer and lidar networks for aerosol profiling and aviation safety the German contribution

Exam 2: Cloud Physics April 16, 2008 Physical Meteorology Questions 1-10 are worth 5 points each. Questions are worth 10 points each.

An investigation into the aerosol dispersion effect through the activation process in marine stratus clouds

Ice nucleation and droplet formation by bare and coated soot particles

Lab 4 Major Anions In Atmospheric Aerosol Particles

AMMA SOP. ITD and HL survey flights (I1.1)

Introduction. Effect of aerosols on precipitation: - challenging problem - no agreement between the results (quantitative and qualitative)

Lidar, sonde and aircraft observations of volcanic ash in Switzerland

Aerosol. Challenge: Global Warming. Observed warming during 20 th century, Tapio. 1910s. 1950s. 1990s T [Kelvin]

Climate impacts of ice nucleation

Trends in the Saharan Air Layer Composition Observed at Izaña - Tenerife

Volcanic Ash Cloud Observations with the DLR- Falcon over Europe during Air Space Closure

Meteorological Applications of Unmanned Aerial Systems

WMO Aeronautical Meteorology Scientific Conference 2017

Name of research institute or organization: Laboratory of Atmospheric Chemistry, Paul Scherrer Institut, CH-5232 Villigen PSI, Switzerland

Slides partly by Antti Lauri and Hannele Korhonen. Liquid or solid particles suspended in a carrier gas Described by their

The AQUAVIT formal intercomparison of atmospheric water measurement methods

Precipitation. GEOG/ENST 2331 Lecture 12 Ahrens: Chapter 7

Transcription:

Name of research institute or organization: Technische Universität Darmstadt, Institut für Angewandte Geowissenschaften, Umweltmineralogie Title of project: In-situ environmental scanning electron microscopic investigation of the ice nucleating abilities of aerosol particles from mixed-phase clouds from the CLACE 6 campaign Project leader and team: Dr. Martin Ebert, Dr. Annette Worringen, Dr. Nathalie Benker, Dipl.-Met. Dörthe Müller-Ebert, Dr. Frank Zimmermann and Prof. Dr. S. Weinbruch (project leader) Project description: The aerosol-cloud interaction processes in mixed-phase clouds were studied during the CLCE 6 campaign in February/March 2007 at the high alpine research station Jungfraujoch. During the CLACE 5 campaign we have performed individual particle analysis of ice residuals, which were sampled by an ice-counterflow virtual impactor (ice-cvi), developed by the Institute for Tropospheric Research in Leipzig (Mertes et al., 2007). The main focus of our electron microscopic work during CLACE 6 lies on the in-situ environmental scanning electron microscopic investigation of the ice nucleating abilities of ice resiudials sampled during the CLACE 6 campaign. Additionally, the single particle analysis approach is used for the chemical identification of the ice forming fraction and to characterize the remaining interstitial particle fraction of the total aerosol in mixed-phase clouds. For particle sampling we have used two self constructed 2-stage impactors (cut off diameters 0.9 µm and 0.06 µm) behind different inlet systems. The interstitial aerosol was sampled behind an interstitial inlet operated with a PM2 cyclone impactor. An ICE-CVI (Counterflow Virtual Impactor) inlet was used to sample resiudal particles of small ice nuclei (IN). For the electron microscopical analysis a FEI Quanta 200 FEG environmental scanning electron microscope (ESEM) and a JEOL J3010 transmission electron microscope (TEM) each combined with energy dipsersive X-ray analysis (EDX) were used. Pb-containing agglomerates The most obvious difference between IN- and interstitial-samples, observed in the CLACE 5 campaign, was the enhanced occurrence of Pb-containing particles in the IN-samples. These particles are predominantly internally mixed with (aged) sea salt, carbonaceous particles or silicates. Our observation of these lead-containing particles in the IN-fraction is in agreement with findings of other participants of the CLACE 5 campaign. As a possible source for the lead component in these particles aircraft emissions are assumed, because lead is still added as additive to avitation gasoline. The potential behaviour of Pb-containing particles as ice nuclei is discussed by Szymer and Zawadzki [1997]. 103

The phase composition of the Pb containing particles could be identified with TEM. In Figure 1-left a section of an aged sea salt particle with small Pb-containing inclusions (black dots) are shown. The Pb inclusions are generally smaller than 10 nm (with a maximum at 5-6 nm), what prevents the direct phase determination of the Pb containing phase by selected area electron diffraction. According to high-resolution images in the TEM and pseudo electron diffraction patterns, obtained by Fourier transformation of the bright field images (see Figure 1-right), the predominant part of the Pb inclusions could be identified as PbS and in single cases as elemental Pb. 5 nm Figure1: (left) TEM-bright field image; section of an aged sea salt particle with Pbcontaining particles (black dots); (right) TEM-bright field image and pseudo electron diffraction pattern of PbS inclusions. First ice activation experiments First in-situ ice nucleating experiments in the ESEM of ice resiudial samples from the CLACE 6 campaign were performed. For this purpose IN samples (ice-cvi) were collected on silicon substrates. These samples were transferred in the environmental scanning electron microscope. Environmental scanning electron microscopy (ESEM) enables in-situ observation of interactions between water vapor and aerosol particles in the sub-micrometer range (e.g., Ebert et al., 2002). By varying the water partial pressure and using a Peltier element to realize temperatures below the freezing point it is possible to obtain supersaturated conditions relative to ice in the sample chamber of such an instrument (Zimmermann et al., 2007). Ice nucleation experiments of the CLACE 6 ice-cvi samples were performed at temperatures between -13 C and -21 C. The temperature was changed in steps of 1K, and at each temperature the H 2 O vapor pressure was increased from subsaturation to supersaturation values (relative to ice). The special 104

design of the vacuum system allows working pressures up to approximately 40 hpa in the sample chamber during imaging with secondary and backscattered electrons. The working pressure can be set by any non-flammable and non-corrosive gas including H 2 O. In our experiments, the total pressure in the sample chamber was always equal to the partial pressure of H 2 O, i.e., no other gas species was present inside the sample chamber. Prior to the ice nucleation experiments, the temperature of the Peltier element was calibrated by determination of the deliquescence relative humidity (DRH) of different salts (Ebert et al., 2002). In order to check that ice nucleation is initiated by the particles, an experiment with a pure silicon substrate (i.e., without particles) was performed. In this case, ice formation was not observed, even at high supersaturation values up to approximately 140 % (relative to ice). More details of the calibration procedures and ice nucleation experiments are given by Zimmermann et al. (2007). sampling sampling particle Ice nucleation observed start end diameter (µm) -13 C -17 C -21 C 02/24/07 02/25/07 > 0.9 Yes Yes Yes 02/24/07 02/25/07 0.06 0.9 No No No 02/25/07 02/26/07 > 0.9 No No No 02/25/07 02/26/07 0.06 0.9 No No No 02/26/07 02/27/07 > 0.9 No No No 02/26/07 02/27/07 0.06 0.9 No No No 02/27/07 02/28/07 > 0.9 No No No 02/28/07 03/01/07 > 0.9 No No No 03/06/07 03/06/07 > 0.9 Yes Yes Yes 03/08/07 03/08/07 0.06 0.9 No No No 03/09/07 03/10/07 > 0.9 No No No Table 1: Results of the in-situ ice nucleating experiments of ice residual samples from the CLACE 6 campaign. In total 33 ice nucleating experiments of eleven IN samples (ice-cvi inlet system) at three different temperatures (-13 C, -17 C, and -21 C) were performed. Unexpectedly, ice nucleation could be observed only for 2 of these 11 samples (see Figure 2). For all other samples no growing ice crystals could be observed, even at supersaturation values (relative to ice) and temperatures of -21 C. It is important to notice in this context that in these ESEM in-situ ice nucleating experiments only ice formation by the condensation freezing and deposition freezing 105

modes can be reproduced. Other ice forming processes like contact or immersion freezing are not possible to follow by this method. Further on, in some cases, activation of a particle is not reproducible, i.e., a particle that acted as an ice nucleus cannot be activated in further cycles (e.g., Soulage, 1957). Figure 2: Reactivated ice residual particle from the CLACE 6 campaign (6 th of March 2007). References Ebert, M., M. Inerle-Hof, and S. Weinbruch, Environmental scanning electron microscopy as a new technique to determine the hygroscopic behaviour of individual aerosol particles, Atmos. Environ. 36, 5909-5916, 2002. Mertes S., B. Verheggen, S. Walter, M. Ebert, P. Conolly, E. Weingartner, J. Schneider, K. Bower, S. Weinbruch, J. Cozic, J. Heintzenberg, Counterflow virtual impactor based collection of small ice particles in mixed-phase clouds for the physico-chemical characterisation of tropospheric ice nuclei: sampler description and first case study, Aerosol Sci. Technol. 41, 9, 848-864, 2007. Soulage, G., Les noyaux de conge lation de l atmosphe` re, Annales de Geophysique 13, 103 134, 167 185, 1957. Szymer W. and I. Zawadzki, Biogenic and anthropogenic Sources of Ice-Forming Nuclei: A Review, Bulletin of the American Meteorological Society, 1997, 209-228. Zimmermann F., M. Ebert, A. Worringen, S. Weinbruch, Environmental scanning electron microscopy (ESEM) as a new tool to determine the ice nucleation capability of individual aerosol particles, Atmospheric Environment 41, 8219-8227, 2007. 106

Key words: Ice nuclei, ESEM, individual particle analysis, chemical composition International Foundation HFSJG Collaborating partners/networks: Institut für Troposphären Forschung, Leipzig, Germany Institut für Physik der Atmosphäre, Johannes Gutenberg-University und Max-Planck Institut für Chemie, Mainz, Germany Institute for Atmospheric and Climate Science, ETH Zurich, Switzerland Scientific publications and public outreach 2007: Refereed journal articles Mertes S., B. Verheggen, S. Walter, M. Ebert, P. Conolly, E. Weingartner, J. Schneider, K. Bower, S. Weinbruch, J. Cozic, J. Heintzenberg, Counterflow virtual impactor based collection of small ice particles in mixed-phase clouds for the physico-chemical characterisation of tropospheric ice nuclei: sampler description and first case study, Aerosol Sci. Technol. 41, 9, 848-864, 2007. Zimmermann F., M. Ebert, A. Worringen, S. Weinbruch, Environmental scanning electron microscopy (ESEM) as a new tool to determine the ice nucleation capability of individual aerosol particles, Atmospheric Environment 41, 8219-8227, 2007. Conference paper Worringen, A., N. Benker, M. Ebert, F. Zimmermann, S. Mertes, E. Weingartner, and S. Weinbruch, Characterization of ice residuals from the CLACE 5 experiment, EAC Salzburg, 2007. Address: TU-Darmstadt Institut für Angewandte Geowissenschaften Fachgebiet Umweltmineralogie Schnittspahnstr. 9 64287 Darmstadt Contacts: Martin Ebert (mebert@geo.tu-darmstadt.de) 107

108