Acidic processing of fly ash: chemical characterization, morphology, and immersion freezing.

Fly ash can undergo aging in the atmosphere through interactions with sulfuric acid and water. These reactions could result in chemical and physical changes that could affect the cloud condensation or ice nucleation activity of fly ash particles. To explore this process, different water and acid treated fly ash types were characterized with X-ray diffraction (XRD), transmission electron microscopy (TEM), electron dispersive spectroscopy (EDS), selected area diffraction (SAED), and inductively coupled plasma atomic emission spectroscopy (ICP-AES).

Heating-Induced Transformations of Atmospheric Particles: Environmental Transmission Electron Microscopy Study.

Environmental transmission electron microscopy was employed to probe transformations in the size, morphology, and composition of individual atmospheric particles as a function of temperature. Two different heating devices were used and calibrated in this work: a furnace heater and a Micro Electro Mechanical System heater. The temperature calibration used sublimation temperatures of NaCl, glucose, and ammonium sulfate particles, and the melting temperature of tin.

Chemical and physical transformations of aluminosilicate clay minerals due to acid treatment and consequences for heterogeneous ice nucleation.

Mineral dust aerosol is one of the largest contributors to global ice nuclei, but physical and chemical processing of dust during atmospheric transport can alter its ice nucleation activity. In particular, several recent studies have noted that sulfuric and nitric acids inhibit heterogeneous ice nucleation in the regime below liquid water saturation in aluminosilicate clay minerals. We have exposed kaolinite, KGa-1b and KGa-2, and montmorillonite, STx-1b and SWy-2, to aqueous sulfuric and nitric acid to determine the physical and chemical changes that are responsible for the observed deactivation.

Cryo-transmission electron microscopy imaging of the morphology of submicrometer aerosol containing organic acids and ammonium sulfate.

The effects of aerosol particles on heterogeneous atmospheric chemistry and climate are determined in part by the internal arrangement of compounds within the particles. To characterize the morphology of internally mixed aerosol particles in the accumulation mode size regime, we have used cryo-transmission electron microscopy to investigate the phase separation behavior of dry, submicrometer particles composed of ammonium sulfate mixed with carboxylic acids (adipic, azelaic, citric, glutaric, malonic, pimelic, suberic, and succinic acid). Determining the morphology of dry particles is important for understanding laboratory studies of aerosol optical properties, reactivity, and cloud condensation nucleus activity, results from field instruments where aerosol particles are dried prior to analysis, and atmospheric processes like deposition mode heterogeneous ice nucleation that occur on dried particles.

Size dependence of the structure of organic aerosol.

The effects of aerosol particles on heterogeneous atmospheric chemistry and climate are determined in part by the internal arrangement of compounds within the particles. We have used cryo-transmission electron microscopy to investigate the phase separation behavior of model organic aerosol composed of ammonium sulfate internally mixed with succinic or pimelic acid. We have found that no particle with a diameter <170 nm for succinic acid and 270 nm for pimelic acid is phase separated.

The necessity of microscopy to characterize the optical properties of size-selected, nonspherical aerosol particles.

It is currently unknown whether mineral dust causes a net warming or cooling effect on the climate system. This uncertainty stems from the varied and evolving shape and composition of mineral dust, which leads to diverse interactions of dust with solar and terrestrial radiation. To investigate these interactions, we have used a cavity ring-down spectrometer to study the optical properties of size-selected calcium carbonate particles, a reactive component of mineral dust.