Aerosolized algal bloom toxins are not inert.

Harmful algal blooms (HABs) are projected to become increasingly prevalent, extending over longer periods and wider geographic regions due to the warming surface ocean water and other environmental factors, including but not limited to nutrient concentrations and runoff for marine and freshwater environments. Incidents of respiratory distress linked to the inhalation of marine aerosols containing HAB toxins have been documented, though the risk is typically associated with the original toxins. However, aerosolized toxins in micrometer and submicrometer particles are vulnerable to atmospheric processing.

Improving FAPbBr Perovskite Crystal Quality via Additive Engineering for High Voltage Solar Cell over 1.5 V.

Lead bromide-based perovskites are promising materials as the top cells of tandem solar cells and for application in various fields requiring high voltages owing to their wide band gaps and excellent environmental resistances. However, several factors, such as the formation of bulk and surface defects, impede the performances of corresponding devices, thereby limiting the efficiencies of these devices as single-junction devices. To reduce the number of defect sites, urea is added to the formamidinium lead bromide (FAPbBr) perovskite material to increase its grain size.

Leaves are a Source of Biogenic Persistent Free Radicals.

Nonsenescent and senescent leaves of selected coniferous and broadleaf plants contained substantial levels of naturally occurring persistent free radicals (PFRs). These biogenic PFRs (BPFRs) were stable and persistent despite multiple wetting and drying cycles, implying that BPFRs can leach and sorb on soil particles. Results suggest that endogenous chemicals in plants and their transformation byproducts can stabilize unpaired electrons in leaves under ambient conditions.

A MEMS-enabled portable gas chromatography injection system for trace analysis.

Growing concerns about environmental conditions, public health, and disease diagnostics have led to the rapid development of portable sampling techniques to characterize trace-level volatile organic compounds (VOCs) from various sources. A MEMS-based micropreconcentrator (μPC) is one such approach that drastically reduces the size, weight, and power constraints offering greater sampling flexibility in many applications. However, the adoption of μPCs on a commercial scale is hindered by a lack of thermal desorption units (TDUs) that easily integrate μPCs with gas chromatography (GC) systems equipped with a flame ionization detector (FID) or a mass spectrometer (MS).

Temperature dependence of the gas-particle partitioning of selected VOCs.

The gas-particle partitioning coefficients for volatile organic compounds (VOCs) are difficult to acquire because discriminating the small mass fraction of the VOCs in the aerosol particle relative to that in the gas phase is challenging. In this paper, we report the temperature dependence of the gas-particle partitioning coefficient (Kp) for n-butanol (n-BuOH) and trichloroethylene (TCE). Using the bench-scale system that we developed, we measured the Kp of surrogate VOCs, n-BuOH, and TCE onto inorganic (ammonium sulfate, Am Sulf) and organic (succinic acid, SA) aerosol particles at a fixed relative humidity (RH) of 35%.

A method to measure the partitioning coefficient of volatile organic compounds in nanoparticles.

The partitioning behavior of volatile organic compounds (VOCs) into nanoparticles is less studied compared to those of semivolatile organic compounds (SVOCs) because of the lower concentration of the VOCs that is expected to partition into particles. One challenge in measuring the accurate partition coefficient of VOCs is quantifying their low mass fraction that sorbed on nanoparticles and differentiating them from the high VOC concentrations present in the gas-phase. Systematically characterizing the partitioning coefficient at a specific environmental condition is also difficult when sampling in the field.

Characterization of hazardous and odorous volatiles emitted from scented candles before lighting and when lit.

Scented candles are known to release various volatile organic compounds (VOCs) including both pleasant aromas and toxic components both before lighting (off) and when lit (on). In this study, we explored the compositional changes of volatiles from scented candles under various settings to simulate indoor use. Carbonyl compounds and other VOCs emitted from six different candle types were analyzed under 'on/off' conditions.

Odor and VOC emissions from pan frying of mackerel at three stages: raw, well-done, and charred.

Many classes of odorants and volatile organic compounds that are deleterious to our wellbeing can be emitted from diverse cooking activities. Once emitted, they can persist in our living space for varying durations. In this study, various volatile organic compounds released prior to and during the pan frying of fish (mackerel) were analyzed at three different cooking stages (stage 1 = raw (R), stage 2 = well-done (W), and stage 3 = overcooked/charred (O)).

The reproducibility of indoor air pollution (IAP) measurement: a test case for the measurement of key air pollutants from the pan frying of fish samples.

To assess the robustness of various indoor air quality (IAQ) indices, we explored the possible role of reproducibility-induced variability in the measurements of different pollutants under similar sampling and emissions conditions. Polluted indoor conditions were generated by pan frying fish samples in a closed room. A total of 11 experiments were carried out to measure a list of key variables commonly used to represent indoor air pollution (IAP) indicators such as particulate matter (PM: PM1, PM2.