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The composition of air-exposed surfaces can have a strong impact on air quality and chemical exposure in the indoor environment. Third hand smoke (THS), which includes surface-deposited cigarette smoke residue along with the collection of gases evolved from such residues, is becoming increasingly recognized as an important source of long-term tobacco smoke exposure. While studies have described gas/surface partitioning behaviour and some multiphase reaction systems involving THS, the possibility of time-dependent changes in chemical composition due to chemical reactivity that is endogenous to the deposited film has yet to be investigated. In this study, sidestream cigarette smoke was allowed to deposit on glass surfaces that were either clean or pre-coated with chemicals that may be oxidized by reactive oxygen species found in the smoke. Surface films included a low volatility antioxidant, tris(2-carboxyethyl)phosphine (TCEP), and two compounds relevant to surface films found within buildings, oleic acid (OA) and squalene (SQ). Upon deposition, oxidation products of nicotine, TCEP, OA, and SQ were formed over time periods of hours to weeks. The inherent oxidative potential of cigarette smoke deposited as a THS film can therefore initiate and sustain oxidation chemistry, transforming the chemical composition of surface films over long periods of time after initial smoke deposition. An interpretation of the THS oxidation results is provided in the context of other types of deposited particulate air pollutants with known oxidative potential that may be introduced to indoor environments. Continued study of THS and deposited surface films found indoors should consider the concept that chemical reservoirs found on surfaces may be reactive, that the chemical composition of indoor surface films may be time-dependent, and that the deposition of aerosol particles can act as a mechanism to initiate oxidation in surface films. 

A single crystal growth method for low solubility polycyclic aromatic substrates based on competitive host–guest equilibria is developed. 

Hypothesis: Bile salts exhibit complex concentration-dependent micellization in aqueous solution, rooted in a long-standing hypothesis of increasing size in bile aggregation that has historically focused on the measurement of only one CMC detected by a given method, without resolving successive stepwise aggregates. Whether bile aggregation is continuous or discrete, at what concentration does the first aggregate form, and how many aggregation steps occur, all remain as open questions. Experiments: Bile salt critical micelle concentrations (CMCs) were investigated with NMR chemical shift titrations and a multi-CMC phase separation modeling approach developed herein. The proposed strategy is to establish a correspondence of the phase separation and mass action models to treat the first CMC; subsequent micellization steps, involving larger micelles, are then treated as phase separation events. Findings: The NMR data and the proposed multi-CMC model reveal and resolve multiple closely spaced sequential preliminary, primary, and secondary discrete CMCs in dihydroxy and trihydroxy bile salt systems in basic (pH 12) solutions with a single model of one NMR data set. Complex NMR data are closely explained by the model. Four CMCs are established in deoxycholate below 100 mM (298 K, pH 12): 3.8 ± 0.5 mM, 9.1 ± 0.3 mM, 27 ± 2 mM, and 57 ± 4 mM, while three CMCs were observed in multiple bile systems, also under basic conditions. Global fitting leverages the sensitivity of different protons to different aggregation stages. In resolving these closely spaced CMCs, the method also obtains chemical shifts of these spectroscopically inaccessible (aka dark) states of the distinct micelles.