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Secondary organic aerosol (SOA) is ubiquitous in the atmosphere and plays a pivotal role in climate, air quality, and health. The production of low-volatility dimeric compounds through accretion reactions is a key aspect of SOA formation. However, despite extensive study, the structures and thus the formation mechanisms of dimers in SOA remain largely uncharacterized. In this work, we elucidate the structures of several major dimer esters in SOA from ozonolysis of a-pinene and b-pinene—substantial global SOA sources—through independent synthesis of authentic standards. We show that these dimer esters are formed in the particle phase and propose a mechanism of nucleophilic addition of alcohols to a cyclic acylperoxyhemiacetal. This chemistry likely represents a general pathway to dimeric compounds in ambient SOA. [ABSTRACT FROM AUTHOR]

This study describes a modeling framework, model evaluation, and source apportionment to understand the causes of Los Angeles (LA) air pollution. A few major updates are applied to the Community Multiscale Air Quality (CMAQ) Model with high spatial resolution (1 km × 1 km). The updates include dynamic traffic emissions based on real-time on-road information and recent emission factors and secondary organic aerosol (SOA) schemes to represent volatile chemical products (VCP). Meteorology is well-predicted compared to ground-based observations, and the emission rates from multiple sources (i.e., on-road, volatile chemical product, area, point, biogenic, and sea spray) are quantified. Evaluation of the CMAQ model shows that ozone is well-predicted despite inaccuracies in nitrogen oxide (NOx) predictions. Particle matter (PM) is underpredicted compared to concurrent measurements made with an aerosol mass spectrometer (AMS) in Pasadena. Inorganic aerosol is well-predicted while SOA is underpredicted. Modeled SOA consists of mostly organic nitrates and products from oxidation of alkane-like intermediate volatility organic compounds (IVOCs) and has missing components that behave like less-oxidized oxygenated organic aerosol (LO-OOA). Source apportionment demonstrates that the urban areas of the LA Basin and vicinity are NOx-saturated (VOC-sensitive) with the largest sensitivity of O3 to changes in VOCs in the urban core. Differing oxidative capacities in different regions impact the nonlinear chemistry leading to PM and SOA formation, which is quantified in this study. [ABSTRACT FROM AUTHOR]

Ambient aerosol size distributions obtained with a compact, scanning mobility analyzer, the "Spider" DMA, are compared to those obtained with a conventional mobility analyzer, with specific attention to the effect of mobility resolution on the measured size distribution parameters. The Spider is a 12-cm diameter radial differential mobility analyzer that spans the 10–500 nm size range with 30s mobility scans. It achieves its compact size by operating at a nominal mobility resolution 푅 = 3 (sheath flow = 0.9 L/min, aerosol flow = 0.3 L/min), in place of the higher sheath-to-aerosol flow commonly used. The question addressed here is whether the lower resolution is sufficient to capture the dynamics and key characteristics of ambient aerosol size distributions. The Spider, operated at 푅 = 3 with 30s up and down scans, was collocated with a TSI 3081 long-column mobility analyzer, operated at 푅 = 10 with a 360s sampling duty cycle. Ambient aerosol data were collected over 26 consecutive days of continuous operation, in Pasadena, CA. Over the 20-500 nm size range, the two instruments exhibit excellent correlation in the total particle number concentrations and geometric mean diameters, with regression slopes of 1.13 and 1.00, respectively. Our results suggest that particle sizing at a lower resolution than typically employed is sufficient in obtaining the key properties of ambient size distributions. [ABSTRACT FROM AUTHOR]

Dimeric compounds contribute significantly to the formation and growth of atmospheric secondary organic aerosol (SOA) derived from monoterpene oxidation. However, the mechanisms of dimer production, in particular the relevance of gas- vs. particle-phase chemistry, remain unclear. Here, through a combination of mass spectrometric, chromatographic, and synthetic techniques, we identify a suite of dimeric compounds (C15-19H24-32O5-11) formed from concerted O3 and OH oxidation of β-pinene (i.e., accretion of O3- and OH-derived products/intermediates). These dimers account for an appreciable fraction (5.9-25.4%) of the β-pinene SOA mass and are designated as extremely low-volatility organic compounds. Certain dimers, characterized as covalent dimer esters, are conclusively shown to form through heterogeneous chemistry, while evidence of dimer production via gas-phase reactions is also presented. The formation of dimers through synergistic O3 + OH oxidation represents a potentially significant, heretofore-unidentified source of low-volatility monoterpene SOA. This reactivity also suggests that the current treatment of SOA formation as a sum of products originating from the isolated oxidation of individual precursors fails to accurately reflect the complexity of oxidation pathways at play in the real atmosphere. Accounting for the role of synergistic oxidation in ambient SOA formation could help to resolve the discrepancy between the measured atmospheric burden of SOA and that predicted by regional air quality and global climate models. [ABSTRACT FROM AUTHOR]

Stabilized Criegee intermediates react with organic acids in the gas phase and at the air-water interface to form a class of ester hydroperoxides, α-acyloxyalkyl hydroperoxides (αAAHPs). A number of recent studies have proposed the importance of αAAHPs to the formation and growth of secondary organic aerosol (SOA). The chemistry of αAAHPs has not been investigated due to a lack of commercially available chemical standards. In this work, the behavior of αAAHPs in condensed phases is investigated for the first time. Experiments were performed with two synthesized αAAHP species. αAAHPs decomposed rapidly in the aqueous phase, with the rate highly dependent on the solvent, temperature, solution pH, and other compounds present in the solution. The measured 1st-order decomposition rate coefficient varied between 10-3 and 10-5 s-1 under the conditions examined in this work. Elucidation of the reaction mechanism is complicated by byproducts arising from the synthetic procedure, but observations are consistent with a base-catalyzed hydrolysis of αAAHPs. The rapid hydrolysis of αAAHPs observed in this work implies their short lifetimes in ambient cloud and fog waters. Decomposition of αAAHPs likely gives rise to smaller peroxides, such as H2O2. The loss of αAAHPs is also relevant to filter extraction, which is commonly practiced in laboratory experiments, potentially explaining contradictory results reported in the existing literature regarding the importance of αAAHPs in SOA. [ABSTRACT FROM AUTHOR]

Organic peroxides comprise a significant fraction of atmospheric secondary organic aerosol (SOA). Detection and quantification of particle-phase organic peroxides are highly challenging, and current efforts rely significantly on filter extraction and offline mass spectrometry (MS). Here, a novel technique, iodometry-assisted liquid chromatography electrospray ionization mass spectrometry (iodometry-assisted LC-ESI-MS), is developed and evaluated with a class of atmospherically relevant organic peroxides, α-acyloxyalkyl hydroperoxides, synthesized via liquid ozonolysis. Iodometry-assisted LC-ESI-MS unambiguously distinguishes organic peroxides, compensating for the lack of functional group information that can be obtained with MS. This technique can be versatile for a wide spectrum of environmental analytical applications for which a molecular-level identification of organic peroxide is required. Here, iodometry-assisted LC-ESI-MS is applied to the water-soluble organic carbon (WSOC) of α-pinene SOA Unexpectedly, a limited number of detectable compounds in WSOC appear to be organic peroxides, despite the fact that spectroscopy-based iodometry indicates 15% of WSOC mass is associated with organic peroxides. This observation would be consistent with decomposition of multifunctional organic peroxides to small peroxides that can be quantified by spectroscopy-based iodometry but not by LC-ESI-MS. Overall, this study raises concerns regarding filter extraction-based studies, showing that assignment of organic peroxides solely on the basis of MS signatures can be misleading. [ABSTRACT FROM AUTHOR]