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Atmospheric aerosols are complex mixtures of different chemical species, and individual particles exist in many different shapes and morphologies. Together, these characteristics contribute to the aerosol mixing state. This review provides an overview of measurement techniques to probe aerosol mixing state, discusses how aerosol mixing state is represented in atmospheric models at different scales, and synthesizes our knowledge of aerosol mixing state's impact on climate‐relevant properties, such as cloud condensation and ice nucleating particle concentrations, and aerosol optical properties. We present these findings within a framework that defines aerosol mixing state along with appropriate mixing state metrics to quantify it. Future research directions are identified, with a focus on the need for integrating mixing state measurements and modeling.

 

Hydroxyl radical (·OH)-initiated oxidation of isoprene, the most abundant nonmethane hydrocarbon in the atmosphere, is responsible for substantial amounts of secondary organic aerosol (SOA) within ambient fine particles. Fine particulate 2-methyltetrol sulfate diastereoisomers (2-MTSs) are abundant SOA products formed via acid-catalyzed multiphase chemistry of isoprene-derived epoxydiols with inorganic sulfate aerosols under low-nitric oxide conditions. We recently demonstrated that heterogeneous ·OH oxidation of particulate 2-MTSs leads to the particle-phase formation of multifunctional organosulfates (OSs). However, it remains uncertain if atmospheric chemical aging of particulate 2-MTSs induces toxic effects within human lung cells. We show that inhibitory concentration-50 (IC50) values decreased from exposure to fine particulate 2-MTSs that were heterogeneously aged for 0 to 22 days by ·OH, indicating increased particulate toxicity in BEAS-2B lung cells. Lung cells further exhibited concentration-dependent modulation of oxidative stress- and inflammatory-related gene expression. Principal component analysis was carried out on the chemical mixtures and revealed positive correlations between exposure to aged multifunctional OSs and altered expression of targeted genes. Exposure to particulate 2-MTSs alone was associated with an altered expression of antireactive oxygen species (ROS)-related genes (NQO-1, SOD-2, and CAT) indicative of a response to ROS in the cells. Increased aging of particulate 2-MTSs by ·OH exposure was associated with an increased expression of glutathione pathway related genes (GCLM and GCLC) and an anti-inflammatory gene (IL-10). 

Heterogeneous hydroxyl radical (•OH) oxidation is an important aging process for isoprene epoxydiol-derived secondary organic aerosol (IEPOX-SOA) that alters its chemical composition. It was recently demonstrated that heterogeneous •OH oxidation can age single-component particulate methyltetrol sulfates (MTSs), causing ∼55% of the SOA mass loss. However, our most recent study of freshly generated IEPOX-SOA particulate mixtures suggests that the lifetime of the complete IEPOX-SOA mixture against heterogeneous •OH oxidation can be prolonged through the fragmentation of higher-order oligomers. Published studies suggest that the heterogeneous •OH oxidation of IEPOX SOA could affect the organic atmospheric aerosol budget at varying rates, depending on aerosol chemical composition. However, heterogeneous •OH oxidation kinetics for the full IEPOX-SOA particulate mixture have not been reported. Here, we exposed freshly generated IEPOX-SOA particles to heterogeneous oxidation by •OH under humid conditions (relative humidity ∼57%) for 0−15 atmospheric-equivalent days of aging and derived an effective heterogeneous •OH rate coefficient (kOH) of 2.64 ± 0.4 × 10−13 cm^3 molecules−1 s−1. While ∼44% of particulate organic mass of nonoxidized IEPOX-SOA was consumed over the entire 15 day aging period, only <7% was consumed during the initial 10 aging days. By molecular-level chemical analysis, we determined oligomers were consumed at a faster rate (by a factor of 2−4) than monomers. Analysis of aerosol physicochemical properties shows that IEPOX-SOA has a core−shell morphology, and the shell becomes thinner with •OH oxidation. In summary, this study demonstrates that heterogeneous •OH oxidation of IEPOX-SOA particles is a dynamic process in which aerosol chemical composition and physicochemical properties play important roles. 

Methyltetrol sulfates are unique tracers for secondary organic aerosols (SOA) formed from acid-driven multiphase chemistry of isoprene-derived epoxydiols. 2-Methyltetrol sulfate diastereomers (2-MTSs) are the dominant isomers and single most-abundant SOA tracers in atmospheric fine particulate matter (PM2.5), but their atmospheric sinks remain unknown. We investigated the oxidative aging of authentic 2-MTS aerosols by gas-phase hydroxyl radicals (•OH) at a relative humidity of 61 ± 1%. The effective rate constant for this heterogeneous reaction was determined as 4.9 ± 0.6 × 10–13 cm3 molecules–1 s–1, corresponding to an atmospheric lifetime of 16 ± 2 days (assuming an •OH concentration of 1.5 × 106 molecules cm–3). Chemical changes to 2-MTSs were monitored by hydrophilic interaction liquid chromatography interfaced to electrospray ionization high-resolution quadrupole time-of-flight mass spectrometry (HILIC/ESI-HR-QTOFMS). Plausible reaction mechanisms are proposed for previously unknown OSs detected in atmospheric PM2.5 at mass-to-charge ratios (m/z) of 139 (C2H3O5S–), 155 (C2H3O6S–), 169 (C3H5O6S–), 171 (C3H7O6S–), 185 (C3H5O7S–), 199 (C4H7O7S–), 211 (C5H7O7S–), 213 (C5H9O7S–), 227 (C5H7O8S–), 229 (C5H9O8S–), and 231 (C5H11O8S–). Heterogeneous •OH oxidation of 2-MTSs redistributes the particulate sulfur speciation into more oxygenated/functionalized OSs, likely modifying the aerosol physicochemical properties of SOA containing 2-MTSs.