scholarly journals Ice nucleation abilities of soot particles determined with the Horizontal Ice Nucleation Chamber

2018 ◽  
Vol 18 (18) ◽  
pp. 13363-13392 ◽  
Author(s):  
Fabian Mahrt ◽  
Claudia Marcolli ◽  
Robert O. David ◽  
Philippe Grönquist ◽  
Eszter J. Barthazy Meier ◽  
...  
Keyword(s):  
Particle Size ◽  
Water Saturation ◽  
Particle Surface ◽  
Water Vapor Sorption ◽  
Contact Angles ◽  
Ice Nucleation ◽  
Particle Surface Area ◽  
Soot Particles ◽  
Microphysical Properties ◽  
Homogeneous Freezing

Abstract. Ice nucleation by different types of soot particles is systematically investigated over the temperature range from 218 to 253 K relevant for both mixed-phase (MPCs) and cirrus clouds. Soot types were selected to represent a range of physicochemical properties associated with combustion particles. Their ice nucleation ability was determined as a function of particle size using relative humidity (RH) scans in the Horizontal Ice Nucleation Chamber (HINC). We complement our ice nucleation results by a suite of particle characterization measurements, including determination of particle surface area, fractal dimension, temperature-dependent mass loss (ML), water vapor sorption and inferred porosity measurements. Independent of particle size, all soot types reveal absence of ice nucleation below and at water saturation in the MPC regime (T>235 K). In the cirrus regime (T≤235 K), soot types show different freezing behavior depending on particle size and soot type, but the freezing is closely linked to the soot particle properties. Specifically, our results suggest that if soot aggregates contain mesopores (pore diameters of 2–50 nm) and have sufficiently low water–soot contact angles, they show ice nucleation activity and can contribute to ice formation in the cirrus regime at RH well below homogeneous freezing of solution droplets. We attribute the observed ice nucleation to a pore condensation and freezing (PCF) mechanism. Nevertheless, soot particles without cavities of the right size and/or too-high contact angles nucleate ice only at or well above the RH required for homogeneous freezing conditions of solution droplets. Thus, our results imply that soot particles able to nucleate ice via PCF could impact the microphysical properties of ice clouds.

scholarly journals Ice nucleation abilities of soot particles determined with the Horizontal Ice Nucleation Chamber

2018 ◽  
Author(s):  
Fabian Mahrt ◽  
Claudia Marcolli ◽  
Robert O. David ◽  
Philippe Grönquist ◽  
Eszter J. Barthazy Meier ◽  
...  
Keyword(s):  
Particle Size ◽  
Water Saturation ◽  
Particle Surface ◽  
Water Vapor Sorption ◽  
Contact Angles ◽  
Ice Nucleation ◽  
Particle Surface Area ◽  
Soot Particles ◽  
Microphysical Properties ◽  
Homogeneous Freezing

Abstract. Ice nucleation by different types of soot particles is systematically investigated over the temperature range from 218 to 253 K relevant for both mixed-phase (MPCs) and cirrus clouds. Soot types were selected to represent a range of physicochemical properties associated with combustion particles. Their ice nucleation ability was determined as a function of particle size using relative humidity (RH) scans in the Horizontal Ice Nucleation Chamber (HINC). We complement our ice nucleation results by a suite of particle characterization measurements, including determination of particle surface area, fractal dimension, temperature dependent mass loss, water vapor sorption and inferred porosity measurements. Independent of particle size, all soot types reveal absence of ice nucleation below and at water saturation in the MPC regime (T > 235 K). In the cirrus regime (T ≤ 235 K), soot types show different freezing behaviour depending on particle size and soot type, but the freezing is closely linked to the soot particle properties. Specifically, our results suggest that if soot aggregates contain mesopores (pore diameters of 2–50 nm) and have sufficiently low water-soot contact angles, they show ice nucleation activity and can contribute to ice formation in the cirrus regime at RH well below homogeneous freezing of solution droplets. We attribute the observed ice nucleation to a pore condensation and freezing (PCF) mechanism. Nevertheless, soot particles without cavities of the right size and/or too high contact angles nucleate ice only at or well above the RH required for homogeneous freezing conditions of solution droplets. Thus, our results imply that soot particles able to nucleate ice via PCF, could impact the microphysical properties of ice clouds.

scholarly journals Condensed-phase biogenic–anthropogenic interactions with implications for cold cloud formation

2017 ◽  
Vol 200 ◽  
pp. 165-194 ◽  
Author(s):  
Joseph C. Charnawskas ◽  
Peter A. Alpert ◽  
Andrew T. Lambe ◽  
Thomas Berkemeier ◽  
Rachel E. O’Brien ◽  
...  
Keyword(s):  
Freezing Temperature ◽  
Organic Aerosol ◽  
Ice Nucleation ◽  
Mixed Phase ◽  
Cloud Formation ◽  
Fossil Fuel Combustion ◽  
Soot Particles ◽  
Ice Nuclei ◽  
Deliquescence Relative Humidity ◽  
Homogeneous Freezing

Anthropogenic and biogenic gas emissions contribute to the formation of secondary organic aerosol (SOA). When present, soot particles from fossil fuel combustion can acquire a coating of SOA. We investigate SOA–soot biogenic–anthropogenic interactions and their impact on ice nucleation in relation to the particles’ organic phase state. SOA particles were generated from the OH oxidation of naphthalene, α-pinene, longifolene, or isoprene, with or without the presence of sulfate or soot particles. Corresponding particle glass transition (Tg) and full deliquescence relative humidity (FDRH) were estimated using a numerical diffusion model. Longifolene SOA particles are solid-like and all biogenic SOA sulfate mixtures exhibit a core–shell configuration (i.e.a sulfate-rich core coated with SOA). Biogenic SOA with or without sulfate formed ice at conditions expected for homogeneous ice nucleation, in agreement with respectiveTgand FDRH. α-pinene SOA coated soot particles nucleated ice above the homogeneous freezing temperature with soot acting as ice nuclei (IN). At lower temperatures the α-pinene SOA coating can be semisolid, inducing ice nucleation. Naphthalene SOA coated soot particles acted as ice nuclei above and below the homogeneous freezing limit, which can be explained by the presence of a highly viscous SOA phase. Our results suggest that biogenic SOA does not play a significant role in mixed-phase cloud formation and the presence of sulfate renders this even less likely. However, anthropogenic SOA may have an enhancing effect on cloud glaciation under mixed-phase and cirrus cloud conditions compared to biogenic SOA that dominate during pre-industrial times or in pristine areas.

scholarly journals Effect of Home Grinding on Properties of Brewed Coffee

2014 ◽  
Vol 4 (1) ◽  
pp. 77
Author(s):  
Christopher Murray ◽  
Thamara Laredo
Keyword(s):  
Particle Size ◽  
Fourier Transform ◽  
Distribution Density ◽  
Particle Surface ◽  
Particle Surface Area ◽  
Present Evidence ◽  
Caffeine Content ◽  
General Recommendation ◽  
Grinding Time ◽  
Ground Coffee

<p>We present measurements of particle size distribution, density, loss of coffee on brewing and caffeine content in brewed coffee (as measured using Fourier Transform Infrared Spectroscopy) as a function of grinding time using a blade-type grinder. In general, there is not a lack of correlation between coffee properties and grinding for grinding times in excess of 42 s, but mass loss on brewing and caffeine content are both increased with grinding times between 0 and 42 s. In addition, we present evidence that this dependence of the composition of brewed coffee on grinding time is a function of increased coffee particle surface area that results from grinding, rather than increased loss of grounds into the brewed beverage or increased percolation time. Finally, we present a general recommendation for determining equivalency between small amounts of finely ground coffee and larger amounts of coarser-ground coffee.</p>

scholarly journals Heterogeneous ice nucleation of viscous secondary organic aerosol produced from ozonolysis of <i>α</i>-pinene

2016 ◽  
Vol 16 (10) ◽  
pp. 6495-6509 ◽  
Author(s):  
Karoliina Ignatius ◽  
Thomas B. Kristensen ◽  
Emma Järvinen ◽  
Leonid Nichman ◽  
Claudia Fuchs ◽  
...  
Keyword(s):  
Secondary Organic Aerosol ◽  
Solid Phase ◽  
Particle Surface ◽  
Amorphous Solid ◽  
Organic Aerosol ◽  
Ice Nucleation ◽  
Cloud Formation ◽  
Particle Surface Area ◽  
Semi Solid ◽  
Heterogeneous Ice Nucleation

Abstract. There are strong indications that particles containing secondary organic aerosol (SOA) exhibit amorphous solid or semi-solid phase states in the atmosphere. This may facilitate heterogeneous ice nucleation and thus influence cloud properties. However, experimental ice nucleation studies of biogenic SOA are scarce. Here, we investigated the ice nucleation ability of viscous SOA particles. The SOA particles were produced from the ozone initiated oxidation of α-pinene in an aerosol chamber at temperatures in the range from −38 to −10 °C at 5–15 % relative humidity with respect to water to ensure their formation in a highly viscous phase state, i.e. semi-solid or glassy. The ice nucleation ability of SOA particles with different sizes was investigated with a new continuous flow diffusion chamber. For the first time, we observed heterogeneous ice nucleation of viscous α-pinene SOA for ice saturation ratios between 1.3 and 1.4 significantly below the homogeneous freezing limit. The maximum frozen fractions found at temperatures between −39.0 and −37.2 °C ranged from 6 to 20 % and did not depend on the particle surface area. Global modelling of monoterpene SOA particles suggests that viscous biogenic SOA particles are indeed present in regions where cirrus cloud formation takes place. Hence, they could make up an important contribution to the global ice nucleating particle budget.

scholarly journals Effect of particle surface area on ice active site densities retrieved from droplet freezing spectra

2016 ◽  
Vol 16 (20) ◽  
pp. 13359-13378 ◽  
Author(s):  
Hassan Beydoun ◽  
Michael Polen ◽  
Ryan C. Sullivan
Keyword(s):  
Surface Area ◽  
Active Sites ◽  
Particle Surface ◽  
Active Surface ◽  
Freezing Temperature ◽  
Ice Nucleation ◽  
Critical Surface ◽  
Cold Plate ◽  
Particle Surface Area ◽  
Immersion Freezing

Abstract. Heterogeneous ice nucleation remains one of the outstanding problems in cloud physics and atmospheric science. Experimental challenges in properly simulating particle-induced freezing processes under atmospherically relevant conditions have largely contributed to the absence of a well-established parameterization of immersion freezing properties. Here, we formulate an ice active, surface-site-based stochastic model of heterogeneous freezing with the unique feature of invoking a continuum assumption on the ice nucleating activity (contact angle) of an aerosol particle's surface that requires no assumptions about the size or number of active sites. The result is a particle-specific property g that defines a distribution of local ice nucleation rates. Upon integration, this yields a full freezing probability function for an ice nucleating particle. Current cold plate droplet freezing measurements provide a valuable and inexpensive resource for studying the freezing properties of many atmospheric aerosol systems. We apply our g framework to explain the observed dependence of the freezing temperature of droplets in a cold plate on the concentration of the particle species investigated. Normalizing to the total particle mass or surface area present to derive the commonly used ice nuclei active surface (INAS) density (ns) often cannot account for the effects of particle concentration, yet concentration is typically varied to span a wider measurable freezing temperature range. A method based on determining what is denoted an ice nucleating species' specific critical surface area is presented and explains the concentration dependence as a result of increasing the variability in ice nucleating active sites between droplets. By applying this method to experimental droplet freezing data from four different systems, we demonstrate its ability to interpret immersion freezing temperature spectra of droplets containing variable particle concentrations. It is shown that general active site density functions, such as the popular ns parameterization, cannot be reliably extrapolated below this critical surface area threshold to describe freezing curves for lower particle surface area concentrations. Freezing curves obtained below this threshold translate to higher ns values, while the ns values are essentially the same from curves obtained above the critical area threshold; ns should remain the same for a system as concentration is varied. However, we can successfully predict the lower concentration freezing curves, which are more atmospherically relevant, through a process of random sampling from g distributions obtained from high particle concentration data. Our analysis is applied to cold plate freezing measurements of droplets containing variable concentrations of particles from NX illite minerals, MCC cellulose, and commercial Snomax bacterial particles. Parameterizations that can predict the temporal evolution of the frozen fraction of cloud droplets in larger atmospheric models are also derived from this new framework.

scholarly journals Overview of Ice Nucleating Particles

2017 ◽  
Vol 58 ◽  
pp. 1.1-1.33 ◽  
Author(s):  
Zamin A. Kanji ◽  
Luis A. Ladino ◽  
Heike Wex ◽  
Yvonne Boose ◽  
Monika Burkert-Kohn ◽  
...  
Keyword(s):  
Chemical Properties ◽  
Ice Nucleation ◽  
Ice Crystal ◽  
New Developments ◽  
Particle Properties ◽  
Microphysical Properties ◽  
Range Transport ◽  
Homogeneous Freezing ◽  
Aerosol Aging ◽  
Physical And Chemical

Abstract Ice particle formation in tropospheric clouds significantly changes cloud radiative and microphysical properties. Ice nucleation in the troposphere via homogeneous freezing occurs at temperatures lower than −38°C and relative humidity with respect to ice above 140%. In the absence of these conditions, ice formation can proceed via heterogeneous nucleation aided by aerosol particles known as ice nucleating particles (INPs). In this chapter, new developments in identifying the heterogeneous freezing mechanisms, atmospheric relevance, uncertainties, and unknowns about INPs are described. The change in conventional wisdom regarding the requirements of INPs as new studies discover physical and chemical properties of these particles is explained. INP sources and known reasons for their ice nucleating properties are presented. The need for more studies to systematically identify particle properties that facilitate ice nucleation is highlighted. The atmospheric relevance of long-range transport, aerosol aging, and coating studies (in the laboratory) of INPs are also presented. Possible mechanisms for processes that change the ice nucleating potential of INPs and the corresponding challenges in understanding and applying these in models are discussed. How primary ice nucleation affects total ice crystal number concentrations in clouds and the discrepancy between INP concentrations and ice crystal number concentrations are presented. Finally, limitations of parameterizing INPs and of models in representing known and unknown processes related to heterogeneous ice nucleation processes are discussed.

scholarly journals Influence of particle size on the ice nucleating ability of mineral dusts

2009 ◽  
Vol 9 (18) ◽  
pp. 6705-6715 ◽  
Author(s):  
A. Welti ◽  
F. Lüönd ◽  
O. Stetzer ◽  
U. Lohmann
Keyword(s):  
Particle Size ◽  
Size Dependence ◽  
Water Saturation ◽  
Mineral Dust ◽  
Ice Nucleation ◽  
Dust Particles ◽  
Ice Nuclei ◽  
Mineral Dusts ◽  
Measured Activation ◽  
Formation Efficiency

Abstract. The recently developed Zurich Ice Nucleation Chamber (ZINC) was used to explore ice nucleation of size-selected mineral dust particles at temperatures between −20°C and −55°C. Four different mineral dust species have been tested: montmorillonite, kaolinite, illite and Arizona test dust (ATD). The selected particle diameters are 100 nm, 200 nm, 400 nm and 800 nm. Relative humidities with respect to ice (RHi) required to activate 1% of the dust particles as ice nuclei (IN) are reported as a function of temperature. An explicit size dependence of the ice formation efficiency has been observed for all dust types. 800 nm particles required the lowest RHi to activate. Deposition nucleation below water saturation was found only below −30°C or −35°C dependent on particle size. Minimum RHi for 1% activation were 105% for illite, kaolinite and montmorillonite at −40°C, respectively 110% for ATD at −45°C. In addition, a possible parameterisation for the measured activation spectra is proposed, which could be used in modeling studies.

INFLUENCE OF PARTICLE SIZE ON THE DYNAMIC STRENGTH OF ELECTRORHEOLOGICAL FLUIDS

1994 ◽  
Vol 08 (20n21) ◽  
pp. 2835-2853 ◽  
Author(s):  
YUNG-HUI SHIH ◽  
HANS CONRAD
Keyword(s):  
Particle Size ◽  
Electric Field ◽  
Volume Fraction ◽  
Low Voltage ◽  
Silicone Oil ◽  
Particle Surface ◽  
Dynamic Strength ◽  
Columnar Structure ◽  
Particle Surface Area ◽  
Polarization Component

The electrical properties, rheology and structure of model ER fluids consisting of glass beads in silicone oil were investigated as a function of electric field E (0–4 kV/mm ), particle size D (6–100 µ m ) and shear rate [Formula: see text]. The conductivity of the suspensions was 3 orders of magnitude greater than that of the host oil at E ⋝ 1 kV/mm ; their low-voltage d.c. permittivity was about 1.35 times larger. The flow stress of the suspensions was given by [Formula: see text] where τE is the polarization component and τ vis the viscous component. The linear dependence of τE on E was attributed to dipole saturation. The observed opposing effects of D and [Formula: see text] on τE were concluded to result from their respective influence on the strength of the columnar structure normally produced by the electric field and its fragmentation during shear. The constant C1 was in agreement with the Einstein equation for the effect of volume fraction of particles on the viscosity of suspensions. The parameter C2/D was concluded to reflect either the effect of particle surface area on viscosity or a polydispersion effect. The present results did not correlate with the Mason number as normally formulated, but did when it was appropriately modified.

scholarly journals Heterogeneous ice nucleation of viscous secondary organic aerosol produced from ozonolysis of α-pinene

2015 ◽  
Vol 15 (24) ◽  
pp. 35719-35752 ◽  
Author(s):  
K. Ignatius ◽  
T. B. Kristensen ◽  
E. Järvinen ◽  
L. Nichman ◽  
C. Fuchs ◽  
...  
Keyword(s):  
Secondary Organic Aerosol ◽  
Solid Phase ◽  
Particle Surface ◽  
Organic Aerosol ◽  
Ice Nucleation ◽  
Cloud Formation ◽  
Cirrus Cloud ◽  
Particle Surface Area ◽  
Semi Solid ◽  
Heterogeneous Ice Nucleation

Abstract. There are strong indications that particles containing secondary organic aerosol (SOA) exhibit amorphous solid or semi-solid phase states in the atmosphere. This may facilitate deposition ice nucleation and thus influence cirrus cloud properties. However, experimental ice nucleation studies of biogenic SOA are scarce. Here, we investigated the ice nucleation ability of viscous SOA particles. The SOA particles were produced from the ozone initiated oxidation of α-pinene in an aerosol chamber at temperatures in the range from −38 to −10 °C at 5–15 % relative humidity with respect to water to ensure their formation in a highly viscous phase state, i.e. semi-solid or glassy. The ice nucleation ability of SOA particles with different sizes was investigated with a new continuous flow diffusion chamber. For the first time, we observed heterogeneous ice nucleation of viscous α-pinene SOA in the deposition mode for ice saturation ratios between 1.3 and 1.4 significantly below the homogeneous freezing limit. The maximum frozen fractions found at temperatures between −36.5 and −38.3 °C ranged from 6 to 20 % and did not depend on the particle surface area. Global modelling of monoterpene SOA particles suggests that viscous biogenic SOA particles are indeed present in regions where cirrus cloud formation takes place. Hence, they could make up an important contribution to the global ice nuclei (IN) budget.

scholarly journals The Role of Contact Angle and Pore Width on Pore Condensation and Freezing

2019 ◽  
Author(s):  
Robert O. David ◽  
Jonas Fahrni ◽  
Claudia Marcolli ◽  
Fabian Mahrt ◽  
Dominik Brühwiler ◽  
...  
Keyword(s):  
Contact Angle ◽  
Active Sites ◽  
Water Saturation ◽  
Capillary Condensation ◽  
Contact Angles ◽  
Ice Nucleation ◽  
Pore Width ◽  
Kelvin Effect ◽  
Pore Condensation

Abstract. It has recently been shown that pore condensation and freezing (PCF) is a mechanism responsible for ice formation under cirrus cloud conditions. PCF is defined as the condensation of liquid water in narrow capillaries below water saturation due to the Kelvin effect, followed by either heterogeneous or homogeneous nucleation depending on the temperature regime and presence of an ice nucleating active site. By using sol-gel synthesized silica with well-defined pore diameters, morphology and distinct chemical surface-functionalization, the role of the water-silica contact angle and pore width on PCF is investigated. We find that contact angle and pore width play an important role in determining the relative humidity required for capillary condensation as predicted by the Kelvin effect and subsequent ice nucleation at cirrus temperatures. For the pore diameters and contact angles covered in this study, 2.2–9.2 nm and 15–78°, respectively, our results reveal that the contact angle plays an important role in predicting the humidity required for pore filling while the pore diameter determines the ability of pore water to freeze. For T > 235 K and below water saturation, pore diameters and contact angles were not able to predict the freezing ability of the particles suggesting an absence of active sites, thus ice nucleation did not proceed via a PCF mechanism. Rather, the ice nucleating ability of the particles depended solely on chemical functionalization. Therefore, parameterizations for the ice nucleating abilities of particles at cirrus conditions should differ from parameterizations at mixed-phase clouds conditions. Our results support PCF as the atmospherically relevant ice nucleation mechanism below water saturation when porous surfaces are encountered in the troposphere.

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