Nitrogen-containing organic carbon (NOC) in atmospheric particles is an important class of brown carbon (BrC). Redox active NOC like aminophenols received little attention in their ability to form BrC. Here we show that iron can catalyze dark oxidative oligomerization of o- and p-aminophenols under simulated aerosol and cloud conditions (pH 1–7, and ionic strength 0.01–1 M). Homogeneous aqueous phase reactions were conducted using soluble Fe(III), where particle growth/agglomeration were monitored using dynamic light scattering. Mass yield experiments of insoluble soot-like dark brown to black particles were as high as 40%. Hygroscopicity growth factors (κ) of these insoluble products under sub- and super-saturated conditions ranged from 0.4–0.6, higher than that of levoglucosan, a prominent proxy for biomass burning organic aerosol (BBOA). Soluble products analyzed using chromatography and mass spectrometry revealed the formation of ring coupling products of o- and p-aminophenols and their primary oxidation products. Heterogeneous reactions of aminophenol were also conducted using Arizona Test Dust (AZTD) under simulated aging conditions, and showed clear changes to optical properties, morphology, mixing state, and chemical composition. These results highlight the important role of iron redox chemistry in BrC formation under atmospherically relevant conditions.

Abstract. In this work, we studied the cloud condensation nuclei (CCN) activity and subsaturated droplet growth of phthalic acid (PTA), isophthalic acid, (IPTA) and terephthalic acid (TPTA), significant benzene polycarboxylic acids and structural isomers found in the atmosphere. Köhler theory (KT) can be effectively applied for hygroscopicity analysis of PTA due to its higher aqueous solubility compared to IPTA and TPTA. As with other hygroscopicity studies of partially water-soluble and effectively water-insoluble species, the supersaturated and subsaturated hygroscopicity derived from KT principles do not agree. To address the disparities in the sub- and supersaturated droplet growth, we developed a new analytical framework called the Hybrid Activity Model (HAM). HAM incorporates the aqueous solubility of a solute within an adsorption-based activation framework. Frenkel–Halsey–Hill (FHH) adsorption theory (FHH-AT) was combined with the aqueous solubility of the compound to develop HAM. Analysis from HAM was validated using laboratory measurements of pure PTA, IPTA, TPTA and PTA–IPTA internal mixtures. Furthermore, the results generated using HAM were tested against traditional KT and FHH-AT to compare their water uptake predictive capabilities. A single hygroscopicity parameter was also developed based on the HAM framework. Results show that the HAM-based hygroscopicity parameter can successfully simulate the water uptake behavior of the pure and internally mixed samples. Results indicate that the HAM framework may be applied to atmospheric aerosols of varying chemical structures and aqueous solubility.

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Understanding the nanoscale water condensation dynamics in strong electric fields is important for improving the atmospheric modeling of cloud dynamics and emerging technologies utilizing electric fields for direct air moisture capture. Here, we use vapor-phase transmission electron microscopy (VPTEM) to directly image nanoscale condensation dynamics of sessile water droplets in electric fields. VPTEM imaging of saturated water vapor stimulated condensation of sessile water nanodroplets that grew to a size of ∼500 nm before evaporating over a time scale of a minute. Simulations showed that electron beam charging of the silicon nitride microfluidic channel windows generated electric fields of ∼10 8 V/m, which depressed the water vapor pressure and effected rapid nucleation of nanosized liquid water droplets. A mass balance model showed that droplet growth was consistent with electric field-induced condensation, while droplet evaporation was consistent with radiolysis-induced evaporation via conversion of water to hydrogen gas. The model quantified several electron beam−sample interactions and vapor transport properties, showed that electron beam heating was insignificant, and demonstrated that literature values significantly underestimated radiolytic hydrogen production and overestimated water vapor diffusivity. This work demonstrates a method for investigating water condensation in strong electric fields and under supersaturated conditions, which is relevant to vapor−liquid equilibrium in the troposphere. While this work identifies several electron beam−sample interactions that impact condensation dynamics, quantification of these phenomena here is expected to enable delineating these artifacts from the physics of interest and accounting for them when imaging more complex vapor−liquid equilibrium phenomena with VPTEM.

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