Search Results
Variability in the mass absorption cross section of black carbon (BC) aerosols is driven by BC internal mixing state at a central European background site (Melpitz, Germany) in winter
2021, Yuan, Jinfeng, Modini, Robin Lewis, Zanatta, Marco, Herber, Andreas B., Müller, Thomas, Wehner, Birgit, Poulain, Laurent, Tuch, Thomas, Baltensperger, Urs, Gysel-Beer, Martin
Properties of atmospheric black carbon (BC) particles were characterized during a field experiment at a rural background site (Melpitz, Germany) in February 2017. BC absorption at a wavelength of 870 nm was measured by a photoacoustic extinctiometer, and BC physical properties (BC mass concentration, core size distribution and coating thickness) were measured by a single-particle soot photometer (SP2). Additionally, a catalytic stripper was used to intermittently remove BC coatings by alternating between ambient and thermo-denuded conditions. From these data the mass absorption cross section of BC (MACBC) and its enhancement factor (EMAC) were inferred for essentially waterfree aerosol as present after drying to low relative humidity (RH). Two methods were applied independently to investigate the coating effect on EMAC: A correlation method (MACBC; ambient vs. BC coating thickness) and a denuding method (MACBC; ambient vs. MACBC; denuded). Observed EMAC values varied from 1.0 to 1.6 (lower limit from denuding method) or 1:2 to 1.9 (higher limit from correlation method), with the mean coating volume fraction ranging from 54% to 78% in the dominating mass equivalent BC core diameter range of 200?220 nm.MACBC and EMAC were strongly correlated with coating thickness of BC. By contrast, other potential drivers of EMAC variability, such as different BC sources (air mass origin and absorption Angström exponent), coating composition (ratio of inorganics to organics) and BC core size distribution, had only minor effects. These results for ambient BC measured at Melpitz during winter show that the lensing effect caused by coatings on BC is the main driver of the variations in MACBC and EMAC, while changes in other BC particle properties such as source, BC core size or coating composition play only minor roles at this rural background site with a large fraction of aged particles. Indirect evidence suggests that potential dampening of the lensing effect due to unfavorable morphology was most likely small or even negligible.
Evaporation of sulfate aerosols at low relative humidity
2017, Tsagkogeorgas, Georgios, Roldin, Pontus, Duplissy, Jonathan, Rondo, Linda, Tröstl, Jasmin, Slowik, Jay G., Ehrhart, Sebastian, Franchin, Alessandro, Kürten, Andreas, Amorim, Antonio, Bianchi, Federico, Kirkby, Jasper, Petäjä, Tuukka, Baltensperger, Urs, Boy, Michael, Curtius, Joachim, Flagan, Richard C., Kulmala, Markku, Donahue, Neil M., Stratmann, Frank
Evaporation of sulfuric acid from particles can be important in the atmospheres of Earth and Venus. However, the equilibrium constant for the dissociation of H2SO4 to bisulfate ions, which is the one of the fundamental parameters controlling the evaporation of sulfur particles, is not well constrained. In this study we explore the volatility of sulfate particles at very low relative humidity. We measured the evaporation of sulfur particles versus temperature and relative humidity in the CLOUD chamber at CERN. We modelled the observed sulfur particle shrinkage with the ADCHAM model. Based on our model results, we conclude that the sulfur particle shrinkage is mainly governed by H2SO4 and potentially to some extent by SO3 evaporation. We found that the equilibrium constants for the dissociation of H2SO4 to HSO4-(KH2SO4) and the dehydration of H2SO4 to SO3 (KSO3) are KH2SO4 Combining double low line 2-4 × 109 kg-1 and KSO3 ≥ 1.4 × g 1010 at 288.8± 5K.
Observation of viscosity transition in α-pinene secondary organic aerosol
2016, Järvinen, Emma, Ignatius, Karoliina, Nichman, Leonid, Kristensen, Thomas B., Fuchs, Claudia, Hoyle, Christopher R., Höppel, Niko, Corbin, Joel C., Craven, Jill, Duplissy, Jonathan, Ehrhart, Sebastian, El Haddad, Imad, Frege, Carla, Gordon, Hamish, Jokinen, Tuija, Kallinger, Peter, Kirkby, Jasper, Kiselev, Alexei, Naumann, Karl-Heinz, Petäjä, Tuukka, Pinterich, Tamara, Prevot, Andre S.H., Saathoff, Harald, Schiebel, Thea, Sengupta, Kamalika, Simon, Mario, Slowik, Jay G., Tröstl, Jasmin, Virtanen, Annele, Vochezer, Paul, Vogt, Steffen, Wagner, Andrea C., Wagner, Robert, Williamson, Christina, Winkler, Paul M., Yan, Chao, Baltensperger, Urs, Donahue, Neil M., Flagan, Rick C., Gallagher, Martin, Hansel, Armin, Kulmala, Markku, Stratmann, Frank, Worsnop, Douglas R., Möhler, Ottmar, Leisner, Thomas, Schnaiter, Martin
Under certain conditions, secondary organic aerosol (SOA) particles can exist in the atmosphere in an amorphous solid or semi-solid state. To determine their relevance to processes such as ice nucleation or chemistry occurring within particles requires knowledge of the temperature and relative humidity (RH) range for SOA to exist in these states. In the Cosmics Leaving Outdoor Droplets (CLOUD) experiment at The European Organisation for Nuclear Research (CERN), we deployed a new in situ optical method to detect the viscous state of α-pinene SOA particles and measured their transition from the amorphous highly viscous state to states of lower viscosity. The method is based on the depolarising properties of laboratory-produced non-spherical SOA particles and their transformation to non-depolarising spherical particles at relative humidities near the deliquescence point. We found that particles formed and grown in the chamber developed an asymmetric shape through coagulation. A transition to a spherical shape was observed as the RH was increased to between 35 % at −10 °C and 80 % at −38 °C, confirming previous calculations of the viscosity-transition conditions. Consequently, α-pinene SOA particles exist in a viscous state over a wide range of ambient conditions, including the cirrus region of the free troposphere. This has implications for the physical, chemical, and ice-nucleation properties of SOA and SOA-coated particles in the atmosphere.