scholarly journals A new thermal gradient ice nucleation diffusion chamber instrument: design, development and first results using Saharan mineral dust

2009 ◽  
Vol 2 (1) ◽  
pp. 153-179 ◽  
Author(s):  
G. Kulkarni ◽  
S. Dobbie ◽  
J. McQuaid
Keyword(s):  
Thermal Gradient ◽  
Mineral Dust ◽  
Aerosol Particles ◽  
Experimental System ◽  
Diffusion Chamber ◽  
Ice Nucleation ◽  
Experimental Investigations ◽  
Design Development ◽  
Static Mode ◽  
First Results

Abstract. A new Thermal Gradient ice nucleation Diffusion Chamber (TGDC) capable of investigating ice nucleation efficiency of atmospherically important aerosols, termed Ice Nuclei (IN), has been designed, constructed and validated. The TGDC can produce a range of supersaturations with respect to ice (SSi) over the temperature range of −10 to −34°C for sufficiently long time needed to observe the ice nucleation by the aerosol particles. The novel aspect of this new TGDC is that the chamber is run in static mode with aerosol particles supported on a Teflon substrate, which can be raised and lowered in a controlled way through the SSi profile within the chamber, and nucleation events are directly observed using digital photography. The TGDC consists of two ice coated plates to which a thermal gradient is applied to produce the range of SSi. The design of the TGDC gives the ability to understand time-related ice nucleation event information and to perform experiments at different temperatures and SSi conditions for different IN without changing the thermal gradient within the TGDC. The temperature and SSi conditions of the experimental system are validated by observing (NH4)2SO4 deliquescence and the results are in good agreement with the literature data. First results are presented of the onset ice nucleation for mineral dust sampled from the Saharan Desert, including images of nucleation and statistical distributions of onset ice nucleation SSi as a function of temperature. This paper illustrates how useful this new TGDC is for process level studies of ice nucleation and more experimental investigations are needed to better quantify the role of ice formation in the atmosphere.

scholarly journals A new thermal gradient ice nucleation diffusion chamber instrument: design, development and first results using Saharan mineral dust

2009 ◽  
Vol 2 (1) ◽  
pp. 221-229 ◽  
Author(s):  
G. Kulkarni ◽  
S. Dobbie ◽  
J. B. McQuaid
Keyword(s):  
Thermal Gradient ◽  
Mineral Dust ◽  
Experimental System ◽  
Diffusion Chamber ◽  
Ice Nucleation ◽  
Experimental Investigations ◽  
Design Development ◽  
Static Mode ◽  
First Results ◽  
Different Temperatures

Abstract. A new Thermal Gradient ice nucleation Diffusion Chamber (TGDC) capable of investigating ice nucleation efficiency of atmospherically important aerosols, termed Ice Nuclei (IN), has been designed, constructed and validated. The TGDC can produce a range of supersaturations with respect to ice (SSi) over the temperature range of −10 to −34°C for sufficiently long time needed to observe the ice nucleation by the particles. The novel aspect of this new TGDC is that the chamber is run in static mode with aerosol particles supported on a Teflon substrate, which can be raised and lowered in a controlled way through the SSi profile within the chamber, and nucleation events are directly observed using digital photography. The TGDC consists of two ice coated plates to which a thermal gradient is applied to produce the range of SSi. The design of the TGDC gives the ability to understand time-related ice nucleation event information and to perform experiments at different temperatures and SSi conditions for different IN without changing the thermal gradient within the TGDC. The temperature and SSi conditions of the experimental system are validated by observing (NH4)2SO4 deliquescence and the results are in good agreement with the literature data. First results are presented of the onset ice nucleation for mineral dust sampled from the Saharan Desert, including images of nucleation and statistical distributions of onset ice nucleation SSi as a function of temperature. This paper illustrates how useful this new TGDC is for process level studies of ice nucleation and more experimental investigations are needed to better quantify the role of ice formation in the atmosphere.

scholarly journals Ice nucleation by surrogates for atmospheric mineral dust and mineral dust/sulfate particles at cirrus temperatures

2005 ◽  
Vol 5 (3) ◽  
pp. 3391-3436 ◽  
Author(s):  
C. M. Archuleta ◽  
P. J. DeMott ◽  
S. M. Kreidenweis
Keyword(s):  
Sulfuric Acid ◽  
Relative Humidity ◽  
Mineral Dust ◽  
Aerosol Particles ◽  
Diffusion Chamber ◽  
Ice Nucleation ◽  
Dust Particles ◽  
Nucleation Behavior ◽  
Ice Nuclei ◽  
Homogeneous Freezing

Abstract. This study examines the potential role of some types of mineral dust and mineral dust with sulfuric acid coatings as heterogeneous ice nuclei at cirrus temperatures. Commercially-available nanoscale powder samples of aluminum oxide, alumina-silicate and iron oxide were used as surrogates for atmospheric mineral dust particles, with and without multilayer coverage of sulfuric acid. A sample of Asian dust aerosol particles was also studied. Measurements of ice nucleation were made using a continuous-flow ice-thermal diffusion chamber (CFDC) operated to expose size-selected aerosol particles to temperatures between −45 and −60°C and a range of relative humidity above ice-saturated conditions. Pure metal oxide particles supported heterogeneous ice nucleation at lower relative humidities than those required to homogeneously freeze sulfuric acid solution particles at sizes larger than about 50 nm. The ice nucleation behavior of the same metal oxides coated with sulfuric acid indicate heterogeneous freezing at lower relative humidities than those calculated for homogeneous freezing of the diluted particle coatings. The effect of soluble coatings on the ice activation relative humidity varied with the respective uncoated core particle types, but for all types the heterogeneous freezing rates increased with particle size for the same thermodynamic conditions. For a selected size of 200 nm, the natural mineral dust particles were the most effective ice nuclei tested, supporting heterogeneous ice formation at an ice relative humidity of approximately 135%, irrespective of temperature. Modified homogeneous freezing parameterizations and theoretical formulations are shown to have application to the description of heterogeneous freezing of mineral dust-like particles with soluble coatings.

scholarly journals Ice nucleation by surrogates for atmospheric mineral dust and mineral dust/sulfate particles at cirrus temperatures

2005 ◽  
Vol 5 (10) ◽  
pp. 2617-2634 ◽  
Author(s):  
C. M. Archuleta ◽  
P. J. DeMott ◽  
S. M. Kreidenweis
Keyword(s):  
Sulfuric Acid ◽  
Relative Humidity ◽  
Mineral Dust ◽  
Aerosol Particles ◽  
Diffusion Chamber ◽  
Ice Nucleation ◽  
Dust Particles ◽  
Nucleation Behavior ◽  
Ice Nuclei ◽  
Homogeneous Freezing

Abstract. This study examines the potential role of some types of mineral dust and mineral dust with sulfuric acid coatings as heterogeneous ice nuclei at cirrus temperatures. Commercially-available nanoscale powder samples of aluminum oxide, alumina-silicate and iron oxide were used as surrogates for atmospheric mineral dust particles, with and without multilayer coverage of sulfuric acid. A sample of Asian dust aerosol particles was also studied. Measurements of ice nucleation were made using a continuous-flow ice-thermal diffusion chamber (CFDC) operated to expose size-selected aerosol particles to temperatures between -45 and -60°C and a range of relative humidity above ice-saturated conditions. Pure metal oxide particles supported heterogeneous ice nucleation at lower relative humidities than those required to homogeneously freeze sulfuric acid solution particles at sizes larger than about 50 nm. The ice nucleation behavior of the same metal oxides coated with sulfuric acid indicate heterogeneous freezing at lower relative humidities than those calculated for homogeneous freezing of the diluted particle coatings. The effect of soluble coatings on the ice activation relative humidity varied with the respective uncoated core particle types, but for all types the heterogeneous freezing rates increased with particle size for the same thermodynamic conditions. For a selected size of 200 nm, the natural mineral dust particles were the most effective ice nuclei tested, supporting heterogeneous ice formation at an ice relative humidity of approximately 135%, irrespective of temperature. Modified homogeneous freezing parameterizations and theoretical formulations are shown to have application to the description of heterogeneous freezing of mineral dust-like particles with soluble coatings.

scholarly journals Manchester Ice Nucleus Counter (MINC) measurements from the 2007 International workshop on Comparing Ice nucleation Measuring Systems (ICIS-2007)

2011 ◽  
Vol 11 (1) ◽  
pp. 53-65 ◽  
Author(s):  
H. M. Jones ◽  
M. J. Flynn ◽  
P. J. DeMott ◽  
O. Möhler
Keyword(s):  
International Workshop ◽  
Diffusion Chamber ◽  
Ice Nucleation ◽  
Concentric Cylinder ◽  
Measuring Systems ◽  
Colorado State University ◽  
Ice Nuclei ◽  
Nucleus Counter ◽  
First Results ◽  
Order Of Magnitude

Abstract. An ice nucleus counter was developed and constructed to enable investigation of potential ice nucleating materials. The Manchester Ice Nucleus Chamber (MINC) is a concentric-cylinder continuous flow diffusion chamber (CFDC). A full explanation of the MINC instrument is given here, along with first results and a comparison to an established instrument of similar design (Colorado State University CFDC) during sampling of common ice nucleating aerosols at the 2007 International workshop on Comparing Ice nucleation Measuring Systems (ICIS-2007). MINC and CSU-CFDC detected the onset of ice nucleation under similar conditions of temperature and supersaturation for several different types of ice nuclei. Comparisons of the ratio of ice nuclei to total aerosol concentrations as a function of supersaturation with respect to water (SSw) showed agreement within one order of magnitude. Possible reasons for differences between the two instruments relating to differences in their design are discussed, along with suggestions to future improvements to the current design.

scholarly journals Laboratory studies of immersion and deposition mode ice nucleation of ozone aged mineral dust particles

2013 ◽  
Vol 13 (17) ◽  
pp. 9097-9118 ◽  
Author(s):  
Z. A. Kanji ◽  
A. Welti ◽  
C. Chou ◽  
O. Stetzer ◽  
U. Lohmann
Keyword(s):  
Mineral Dust ◽  
Active Surface ◽  
Freezing Temperature ◽  
Ice Nucleation ◽  
Dust Particles ◽  
Laboratory Studies ◽  
Ambient Conditions ◽  
First Results ◽  
Deposition Mode ◽  
Heterogeneous Ice Nucleation

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.

scholarly journals Ice nucleation of ammonia gas exposed montmorillonite mineral dust particles

2007 ◽  
Vol 7 (14) ◽  
pp. 3923-3931 ◽  
Author(s):  
A. Salam ◽  
U. Lohmann ◽  
G. Lesins
Keyword(s):  
Room Temperature ◽  
Mineral Dust ◽  
Diffusion Chamber ◽  
Ice Nucleation ◽  
Dust Particles ◽  
Experimental Conditions ◽  
Activation Temperature ◽  
Ammonia Gas ◽  
Ice Nuclei ◽  
Gas Exposure

Abstract. The ice nucleation characteristics of montmorillonite mineral dust aerosols with and without exposure to ammonia gas were measured at different atmospheric temperatures and relative humidities with a continuous flow diffusion chamber. The montmorillonite particles were exposed to pure (100%) and diluted ammonia gas (25 ppm) at room temperature in a stainless steel chamber. There was no significant change in the mineral dust particle size distribution due to the ammonia gas exposure. 100% pure ammonia gas exposure enhanced the ice nucleating fraction of montmorillonite mineral dust particles 3 to 8 times at 90% relative humidity with respect to water (RHw) and 5 to 8 times at 100% RHw for 120 min exposure time compared to unexposed montmorillonite within our experimental conditions. The percentages of active ice nuclei were 2 to 8 times higher at 90% RHw and 2 to 7 times higher at 100% RHw in 25 ppm ammonia exposed montmorillonite compared to unexposed montmorillonite. All montmorillonite particles are more efficient as ice nuclei with increasing relative humidities and decreasing temperatures. The activation temperature of montmorillonite exposed to 100% pure ammonia was 15°C higher than for unexposed montmorillonite particles at 90% RHw. In the 25 ppm ammonia exposed montmorillonite experiments, the activation temperature was 10°C warmer than unexposed montmorillonite at 90% RHw. Degassing does not reverse the ice nucleating ability of ammonia exposed montmorillonite mineral dust particles suggesting that the ammonia is chemically bound to the montmorillonite particle. This is the first experimental evidence that ammonia gas exposed montmorillonite mineral dust particles can enhance its activation as ice nuclei and that the activation can occur at temperatures warmer than –10°C where natural atmospheric ice nuclei are very scarce.

scholarly journals Characterization of individual ice residual particles by the single droplet freezing method: a case study in the Asian dust outflow region

2018 ◽  
Vol 18 (3) ◽  
pp. 1785-1804 ◽  
Author(s):  
Ayumi Iwata ◽  
Atsushi Matsuki
Keyword(s):  
Atmospheric Aerosols ◽  
Mineral Dust ◽  
Aerosol Particles ◽  
Ice Nucleation ◽  
Asian Dust ◽  
Particle Mixing ◽  
Active Particles ◽  
Nucleation Activity ◽  
Mixing States ◽  
Ice Nucleation Activity

Abstract. In order to better characterize ice nucleating (IN) aerosol particles in the atmosphere, we investigated the chemical composition, mixing state, and morphology of atmospheric aerosols that nucleate ice under conditions relevant for mixed-phase clouds. Five standard mineral dust samples (quartz, K-feldspar, Na-feldspar, Arizona test dust, and Asian dust source particles) were compared with actual aerosol particles collected from the west coast of Japan (the city of Kanazawa) during Asian dust events in February and April 2016. Following droplet activation by particles deposited on a hydrophobic Si (silicon) wafer substrate under supersaturated air, individual IN particles were located using an optical microscope by gradually cooling the temperature to −30 ∘C. For the aerosol samples, both the IN active particles and non-active particles were analyzed individually by atomic force microscopy (AFM), micro-Raman spectroscopy, and scanning electron microscopy (SEM) coupled with energy dispersive X-ray spectroscopy (EDX). Heterogeneous ice nucleation in all standard mineral dust samples tested in this study was observed at consistently higher temperatures (e.g., −22.2 to −24.2 ∘C with K-feldspar) than the homogeneous freezing temperature (−36.5 ∘C). Meanwhile, most of the IN active atmospheric particles formed ice below −28 ∘C, i.e., at lower temperatures than the standard mineral dust samples of pure components. The most abundant IN active particles above −30 ∘C were predominantly irregular solid particles that showed clay mineral characteristics (or mixtures of several mineral components). Other than clay, Ca-rich particles internally mixed with other components, such as sulfate, were also regarded as IN active particle types. Moreover, sea salt particles were predominantly found in the non-active fraction, and internal mixing with sea salt clearly acted as a significant inhibiting agent for the ice nucleation activity of mineral dust particles. Also, relatively pure or fresh calcite, Ca(NO3)2, and (NH4)2SO4 particles were more often found in the non-active fraction. In this study, we demonstrated the capability of the combined single droplet freezing method and thorough individual particle analysis to characterize the ice nucleation activity of atmospheric aerosols. We also found that dramatic changes in the particle mixing states during long-range transport had a complex effect on the ice nucleation activity of the host aerosol particles. A case study in the Asian dust outflow region highlighted the need to consider particle mixing states, which can dramatically influence ice nucleation activity.

scholarly journals Characterization of individual ice nuclei by the single droplet freezing method: a case study in the Asian dust outflow region

2017 ◽  
Author(s):  
Ayumi Iwata ◽  
Atsushi Matsuki
Keyword(s):  
Atmospheric Aerosols ◽  
Mineral Dust ◽  
Aerosol Particles ◽  
Ice Nucleation ◽  
Asian Dust ◽  
Particle Mixing ◽  
Active Particles ◽  
Nucleation Activity ◽  
Mixing States ◽  
Ice Nucleation Activity

Abstract. In order to better characterize ice-nucleating (IN) aerosol particles in the atmosphere, we investigated the chemical composition, mixing state, and morphology of atmospheric aerosols that nucleate ice under conditions relevant for mixed phase clouds. Five standard mineral dust samples (quartz, K-feldspar, Na-feldspar, Arizona test dust, and Asian dust source particles) were compared with actual aerosol particles collected from the west coast of Japan (Kanazawa City) during Asian dust events in February and April 2016. Following droplet activation by particles deposited 5 on a hydrophobic Si wafer substrate under supersaturated air, individual IN particles were located using an optical microscope by gradually cooling the temperature to −30 °C. For the aerosol samples, both the IN active particles and non-active particles were analyzed individually by Atomic Force Microscopy (AFM), micro-Raman spectroscopy, and Scanning Electron Microscopy (SEM) coupled with Energy Dispersive X-ray spectroscopy (EDX). Heterogeneous ice nucleation in all standard mineral dust samples tested in this study was observed at consistently higher temperatures (−25.7 °C) than the homogeneous freezing temperature (−36.5 °C). Meanwhile, most of the IN active atmospheric particles formed ice below −28 °C and were found to be IN active, but slower than the standard mineral dust samples of pure components. The most abundant IN active particles above −30 °C were predominantly irregular solid particles that showed clay mineral characteristics (or mixtures of several mineral components). Other than clay, Ca-rich particles internally mixed with other components, such as sulfate, were also regarded as IN active particle types. Moreover, sea salt particles were predominantly found in the non-active fraction, and internal mixing with sea salt clearly acted as a significant inhibiting agent for the ice nucleation activity of mineral dust particles. Also, relatively pure or fresh calcite, Ca(NO3)2, and (NH4)2SO4 particles were more often found in the non-active fraction. In this study, we demonstrated the capability of the combined single droplet freezing method and thorough individual particle analysis to characterize the ice nucleation activity of atmospheric aerosols. We also found that dramatic changes in the particle mixing states during long-range transport had a complex effect on the ice nucleation activity of the host aerosol particles. A case study in the Asian dust outflow region highlighted the need to consider particle mixing states, which can dramatically influence ice nucleation activity.

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