In contrast to previously published reports, we have detected sustained infectivity of aerosolized influenza viruses in respiratory mucus over a wide-range of relative humidity conditions, indicating a risk of airborne transmission in a broad range of environments.

Phthalates are widely used as plasticizers, and improved ability to predict emissions of phthalates is of interest because of concern about their health effects. An experimental chamber was used to measure emissions of di-2-ethylhexyl-phthalate (DEHP) from vinyl flooring, with ammonium sulfate particles introduced to examine their influence on the emission rate and to measure the partitioning of DEHP onto airborne particles. When particles were introduced to the chamber at concentrations of 100 to 245 μg/m(3), the total (gas + particle) DEHP concentrations increased by a factor of 3 to 8; under these conditions, emissions were significantly enhanced compared to the condition without particles. The measured DEHP partition coefficient to ammonium sulfate particles with a median diameter of 45 ± 5 nm was 0.032 ± 0.003 m(3)/μg (95% confidence interval). The DEHP-particle sorption equilibration time was demonstrated to be less than 1 min. Both the partition coefficient and equilibration time agree well with predictions from the literature. This study represents the first known measurements of the particle-gas partition coefficient for DEHP. Furthermore, the results demonstrate that the emission rate of DEHP is substantially enhanced in the presence of particles. The particles rapidly sorb DEHP from the gas phase, allowing more to be emitted from the source, and also appear to enhance the convective mass-transfer coefficient itself. Airborne particles can influence SVOC fate and transport in the indoor environment, and these mechanisms must be considered in evaluating exposure and human health.

Nanoparticles (NPs) resulting from urban road dust resuspension are an understudied class of pollutants in urban environments with strong potential for health hazards.

In studies that have explored the potential environmental impacts of manufactured nanomaterials, the atmosphere has largely been viewed as an inert setting that acts merely as a route for inhalation exposure. Manufactured nanomaterials will enter the atmosphere during production, use, and disposal, and rather than simply being transported, airborne nanoparticles are in fact subject to physical and chemical transformations that could modify their fate, transport, bioavailability, and toxicity once they deposit to aqueous and terrestrial ecosystems. The objective of this paper is to review the factors affecting carbonaceous nanomaterials' behavior in the environment and to show that atmospheric transformations, often overlooked, have the potential to alter nanoparticles' physical and chemical properties and thus influence their environmental fate and impact. Atmospheric processing of naturally occurring and incidental nanoparticles takes place through coagulation, condensation, and oxidation; these phenomena are expected to affect manufactured nanoparticles as well. It is likely that carbonaceous nanomaterials in the atmosphere will be oxidized, effectively functionalizing them. By influencing size, shape, and surface chemistry, atmospheric transformations have the potential to affect a variety of nanoparticle-environment interactions, including solubility, interaction with natural surfactants, deposition to porous media, and ecotoxicity. Potential directions for future research are suggested to address the current lack of information surrounding atmospheric transformations of engineered nanomaterials.