Microbial volatile organic compounds (MVOCs) play an essential role in many environmental fields, such as indoor air quality. Long-term exposure to odorous and toxic MVOCs can negatively affect the health of occupants. Recently, the involvement of surface reservoirs in indoor chemistry has been realized, which signifies the importance of the phase partitioning of volatile organic pollutants. However, reliable partition coefficients of many MVOCs are currently lacking. Equilibrium partition coefficients, such as Henry's law constant, H, are crucial for understanding the environmental behavior of chemicals. This study aims to experimentally determine the H values and their temperature dependence for key MVOCs under temperature relevant to the indoor environment. The H values were determined with the inert gas-stripping (IGS) method and variable phase ratio headspace (VPR-HS) technique. A two-dimensional partitioning model was applied to predict the indoor phase distribution of MVOCs and potential exposure pathways to the residences. The findings show that the MVOCs are likely distributed between the gas and weakly polar (e.g., organic-rich) reservoirs indoors. Temperature and the volume of reservoirs can sensitively affect indoor partitioning. Our results give a more comprehensive view of indoor chemical partitioning and exposure.

Flavoring agents added to the e-cigarette and hookah have increased the attractiveness of novel nicotine products. Many widely used flavorings are carbonyls, which are toxic to humans. In an indoor...

Biomass burning is a significant contributor to atmospheric pollution, its emissions have been found to have adverse impacts on climate and human health. Largely, these impacts are dictated by how...

Autoxidation is a widely recognized mechanism known to initiate the degradation of food and lipids and modify organic matter in the atmosphere. Given the low NOx concentration in aqueous media (e.g., cloud water and fog droplets), autoxidation can become vital to facilitate the formation of highly oxygenated molecules such as organic peroxides (ROOH and ROOR). Here, we have identified aqueous-phase autoxidation-initiated hydroperoxides in varying organic precursors, including a laboratory model compound and monoterpene oxidation products. Our results show that autoxidation-initiated ROOHs are suppressed at enhanced precursor and oxidant concentrations. Furthermore, we observed an exponential increase in the yield of ROOHs when UV light with longer wavelengths was used in the experiment, comparing UVA, UVB, and UVC. Water-soluble organic compounds represent a significant fraction of ambient cloud water component (up to 500 µM. Thus, aqueous-phase autoxidation can become an important oxidation pathway for water-soluble species and as such facilitate the formation of ROOHs, thereby adding to the climate and health burden of atmospheric particulate matter.

Biomass burning is a significant contributor to atmospheric pollution, its emissions have been found to have adverse impacts on climate and human health. Largely, these impacts are dictated by how the composition of the emissions changes once emitted into the atmosphere. Recently, anhydrides have been identified as a significant fraction of biomass burning emissions, however, little is known about their atmospheric evolution, or their interactions within the burn plume. Without this understanding, it is challenging to predict the impact of anhydrides on biomass burning emissions, and by extension, their influence on climate and health. In this study, we investigate anhydrides as potentially unrecognized electrophiles in the atmosphere. Firstly, by exploring their reactivity towards important biomass burning emitted nucleophiles, and secondly, by measuring their uptake on the emissions themselves. Our results show that phthalic and maleic anhydride can react with a wide range of nucleophiles, including hydroxy and amino-containing compounds, such as levoglucosan or aniline. Additionally, using a coated-wall flow tube setup, we demonstrate that anhydrides reactively uptake to biomass burning films and influence their composition. The anhydride nucleophile reaction was found to be irreversible, proceeding without sunlight or free radicals and indicating it may occur during the day or night time. Furthermore, the reaction products were found to be water-stable and contain functional groups which enhance their mass and likely contribute to the formation of secondary organic aerosol, with knock-on climate effects. Overall, our study sheds light on the fundamental chemistry of anhydrides and their potential impacts in the atmosphere.