Kinetics of Heterogeneous Ice Nucleation on the Surfaces of Mineral Dust Cores Inserted into Aqueous Ammonium Sulfate Particles

2003 ◽  
Vol 107 (9) ◽  
pp. 1296-1306 ◽  
Author(s):  
Hui-Ming Hung ◽  
Adam Malinowski ◽  
Scot T. Martin
2002 ◽  
Vol 106 (2) ◽  
pp. 293-306 ◽  
Author(s):  
Hui-Ming Hung ◽  
Adam Malinowski ◽  
Scot T. Martin

2010 ◽  
Vol 37 (24) ◽  
pp. n/a-n/a ◽  
Author(s):  
Ryan C. Sullivan ◽  
Lorena Miñambres ◽  
Paul J. DeMott ◽  
Anthony J. Prenni ◽  
Christian M. Carrico ◽  
...  

2019 ◽  
Vol 76 (4) ◽  
pp. 1015-1029 ◽  
Author(s):  
Romy Ullrich ◽  
Corinna Hoose ◽  
Daniel J. Cziczo ◽  
Karl D. Froyd ◽  
Joshua P. Schwarz ◽  
...  

Abstract The contribution of heterogeneous ice nucleation to the formation of cirrus cloud ice crystals is still not well quantified. This results in large uncertainties when predicting cirrus radiative effects and their role in Earth’s climate system. The goal of this case study is to simulate the composition, and thus activation conditions, of ice nucleating particles (INPs) to evaluate their contribution to heterogeneous cirrus ice formation in relation to homogeneous ice nucleation. For this, the regional model COSMO—Aerosols and Reactive Trace Gases (COSMO-ART) was used to simulate a synoptic cirrus cloud over Texas on 13 April 2011. The simulated INP composition was then compared to measured ice residual particle (IRP) composition from the actual event obtained during the NASA Midlatitude Airborne Cirrus Properties Experiment (MACPEX) aircraft campaign. These IRP measurements indicated that the dominance of heterogeneous ice nucleation was mainly driven by mineral dust with contributions from a variety of other particle types. Applying realistic activation thresholds and concentrations of airborne transported mineral dust and biomass-burning particles, the model implementing the heterogeneous ice nucleation parameterization scheme of Ullrich et al. is able to reproduce the overall dominating ice formation mechanism in contrast to the model simulation with the scheme of Phillips et al. However, the model showed flaws in reproducing the IRP composition.


2013 ◽  
Vol 13 (17) ◽  
pp. 9097-9118 ◽  
Author(s):  
Z. A. Kanji ◽  
A. Welti ◽  
C. Chou ◽  
O. Stetzer ◽  
U. Lohmann

Abstract. Ice nucleation in the atmosphere is central to the understanding the microphysical properties of mixed-phase and cirrus clouds. Ambient conditions such as temperature (T) and relative humidity (RH), as well as aerosol properties such as chemical composition and mixing state play an important role in predicting ice formation in the troposphere. Previous field studies have reported the absence of sulfate and organic compounds on mineral dust ice crystal residuals sampled at mountain top stations or aircraft based measurements despite the long-range transport mineral dust is subjected to. We present laboratory studies of ice nucleation for immersion and deposition mode on ozone aged mineral dust particles for 233 < T < 263 K. Heterogeneous ice nucleation of untreated kaolinite (Ka) and Arizona Test Dust (ATD) particles is compared to corresponding aged particles that are subjected to ozone concentrations of 0.4–4.3 ppmv in a stainless steel aerosol tank. The portable ice nucleation counter (PINC) and immersion chamber combined with the Zurich ice nucleation chamber (IMCA-ZINC) are used to conduct deposition and immersion mode measurements, respectively. Ice active fractions as well as ice active surface site densities (ns) are reported and observed to increase as a function of decreasing temperature. We present first results that demonstrate enhancement of the ice nucleation ability of aged mineral dust particles in both the deposition and immersion mode due to ageing. We also present the first results to show a suppression of heterogeneous ice nucleation activity without the condensation of a coating of (in)organic material. In immersion mode, low ozone exposed Ka particles showed enhanced ice activity requiring a median freezing temperature of 1.5 K warmer than that of untreated Ka, whereas high ozone exposed ATD particles showed suppressed ice nucleation requiring a median freezing temperature of 3 K colder than that of untreated ATD. In deposition mode, low exposure Ka had ice active fractions of an order of magnitude higher than untreated Ka, whereas high ozone exposed ATD had ice active fractions up to a factor of 4 lower than untreated ATD. From our results, we derive and present parameterizations in terms of ns(T) that can be used in models to predict ice nuclei concentrations based on available aerosol surface area.


2012 ◽  
Vol 12 (5) ◽  
pp. 12531-12621 ◽  
Author(s):  
C. Hoose ◽  
O. Möhler

Abstract. A small subset of the atmospheric aerosol population has the ability to induce ice formation at conditions under which ice would not form without them (heterogeneous ice nucleation). While no closed theoretical description of this process and the requirements for good ice nuclei is available, numerous studies have attempted to quantify the ice nucleation ability of different particles empirically in laboratory experiments. In this article, an overview of these results is provided. Ice nucleation onset conditions for various mineral dust, soot, biological, organic and ammonium sulphate particles are summarized. Typical temperature-supersaturation regions can be identified for the onset of ice nucleation of these different particle types, but the various particle sizes and activated fractions reported in different studies have to be taken into account when comparing results obtained with different methodologies. When intercomparing only data obtained under the same conditions, it is found that dust mineralogy is not a consistent predictor of higher or lower ice nucleation ability. However, the broad majority of studies agrees on a reduction of deposition nucleation by various coatings on mineral dust. The ice nucleation active surface site (INAS) density is discussed as a normalized measure for ice nucleation activity. For most immersion and condensation freezing measurements on mineral dust, estimates of the temperature-dependent INAS density agree within about two orders of magnitude. For deposition nucleation on dust, the spread is significantly larger, but a general trend of increasing INAS densities with increasing supersaturation is found. For soot, the presently available results are divergent. Estimated average INAS densities are high for ice-nucleation active bacteria at high subzero temperatures. At the same time, it is shown that some other biological aerosols, like certain pollen grains and fungal spores, are not intrinsically better ice nuclei than dust, but owe their high ice nucleation onsets to their large sizes. Surface-area-dependent parameterizations of heterogeneous ice nucleation are discussed. For immersion freezing on mineral dust, fitted INAS densities are available, but should not be used outside the temperature interval of the data they were based on. Classical nucleation theory, if employed with one fitted contact angle, does not reproduce the observed temperature dependence for immersion nucleation, temperature and supersaturation dependence for deposition nucleation, and time dependence.


2012 ◽  
Vol 12 (20) ◽  
pp. 9817-9854 ◽  
Author(s):  
C. Hoose ◽  
O. Möhler

Abstract. A small subset of the atmospheric aerosol population has the ability to induce ice formation at conditions under which ice would not form without them (heterogeneous ice nucleation). While no closed theoretical description of this process and the requirements for good ice nuclei is available, numerous studies have attempted to quantify the ice nucleation ability of different particles empirically in laboratory experiments. In this article, an overview of these results is provided. Ice nucleation "onset" conditions for various mineral dust, soot, biological, organic and ammonium sulfate particles are summarized. Typical temperature-supersaturation regions can be identified for the "onset" of ice nucleation of these different particle types, but the various particle sizes and activated fractions reported in different studies have to be taken into account when comparing results obtained with different methodologies. When intercomparing only data obtained under the same conditions, it is found that dust mineralogy is not a consistent predictor of higher or lower ice nucleation ability. However, the broad majority of studies agrees on a reduction of deposition nucleation by various coatings on mineral dust. The ice nucleation active surface site (INAS) density is discussed as a simple and empirical normalized measure for ice nucleation activity. For most immersion and condensation freezing measurements on mineral dust, estimates of the temperature-dependent INAS density agree within about two orders of magnitude. For deposition nucleation on dust, the spread is significantly larger, but a general trend of increasing INAS densities with increasing supersaturation is found. For soot, the presently available results are divergent. Estimated average INAS densities are high for ice-nucleation active bacteria at high subzero temperatures. At the same time, it is shown that INAS densities of some other biological aerosols, like certain pollen grains, fungal spores and diatoms, tend to be similar to those of dust. These particles may owe their high ice nucleation onsets to their large sizes. Surface-area-dependent parameterizations of heterogeneous ice nucleation are discussed. For immersion freezing on mineral dust, fitted INAS densities are available, but should not be used outside the temperature interval of the data they were based on. Classical nucleation theory, if employed with only one fitted contact angle, does not reproduce the observed temperature dependence for immersion nucleation, the temperature and supersaturation dependence for deposition nucleation, and the time dependence of ice nucleation. Formulations of classical nucleation theory with distributions of contact angles offer possibilities to overcome these weaknesses.


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