Potential toxic components in size-resolved particles and gas from residential combustion: Emission factor and health risk.

Particulate matter (PM) from residential combustion is an existential threat to human health. Emission factors (EFs) of multiple potential toxic components (PTCs) in size-resolved PM and gas from eight residential fuel combustion were measured, and size distribution, gas/particle partitioning and health risks of the PTCs were investigated. Average EFs from clean coal and anthracite coal were PTEs (sum of EFs of 11 Potential Toxic Elements, 6.62 mg/kg fuels) > PAHs (sum of 22 Polycyclic Aromatic Hydrocarbons, 1.12 mg/kg) > OPAHs (sum of 5 Oxygenated Polycyclic Aromatic Hydrocarbons, 0.45 mg/kg) > PAEs (sum of 6 Phthalate Esters, 0.11 mg/kg) > NPAHs (sum of 14 Nitropolycyclic Aromatic Hydrocarbons, 16.84 µg/kg) > OPEs (sum of 7 Organophosphate Esters, 7.57 µg/kg) > PCBs (sum of 6 Polychorinated Biphenyls, 0.07 µg/kg), which were 2-3 and 1-2 orders of magnitude lower than the EFs of PTCs (except PTEs) from bituminous coal and biomass. Most PAHs, OPAHs and NPAHs, which may mainly originate from chemical reactions, showed similar size distributions and averagely 85 % concentrated in PM1. PTEs, PAEs, OPEs and PCBs generated from the release from raw fuels may have a higher proportion, so their size distributions were more complex and varied with combustion temperature, volatility of compounds, binding mode of the raw fuels, and so on. In addition, clean coal and high-quality anthracite coal could reduce the health risks from the potential organic toxic components, but also reveal the stumbling block of PTEs in risk control.

Shrinkable Hydrogel-Enhanced Biomarker Detection with X-ray Fluorescent Nanoparticles.

This paper reports a new method to enhance the sensitivity of nanoparticle-based protein detection with X-ray fluorescence by exploiting the large volume reduction of hydrogel upon dehydration. A carboxylated agarose hydrogel with uniaxial microchannels is used to allow rapid diffusion of nanoparticles and biomolecules into the hydrogel and water molecules out of the hydrogel. Carboxylated hydrogels are modified to capture protein biomarkers and X-ray fluorescence nanoparticles (iron oxide nanoparticles) are modified with antibodies that are specific to protein biomarkers. The presence of protein biomarkers in solution binds the nanoparticles on the hydrogel channels. The dehydration of hydrogels leads to a size reduction of over 80 times, which increases the number of nanoparticles in the interaction volume of the primary X-ray beam and the intensity of characteristic X-ray fluorescence signal. A detection limit of 2 µg/mL for protein detection has been established by determining the number of nanoparticles using X-ray fluorescence.

Organic compound source profiles of PM2.5 from traffic emissions, coal combustion, industrial processes and dust.

Eighteen polycyclic aromatic hydrocarbons (PAHs), 24 n-alkanes, 7 hopanes, 2 cholestanes, inorganic ions, elements and carbon fractions were analyzed in real-world source samples of PM2.5 (fine particulate matter) from traffic emissions (gasoline vehicles-TGV, diesel vehicles-TDV, diesel ship-TDS, and heavy oil ships-THOS), coal combustion (coal-fired industrial boilers-CIB, power plants-CPP, and residential stoves-CRS), industrial process emissions (cement industry-IPCI, and steel industry-IPSI), and dust (soil dust-DSD, road dust-DRD, and construction dust-DCD). High molecular weight (sum of five to seven rings) PAHs accounted for higher fractions for TGV (80%) and THS (61%) than for TDV, TDS and coal combustion sources (31%-47%). Hopane ratios (C29αß/C30αß) in coal related sources were mostly higher than 1, whereas that of traffic emissions was lower than 1. The homohopane index [S/(S + R)], which is a useful index for identifying the maturity of fuels, ranked as TGV > THS > TDV and TDS > coal combustion. For n-alkane profiles, coal related sources showed peaks at C16-C19, TDV, TDS and THS showed similar peaks at C17-C25, but peaks for DSD (C30-C32), DRD (C17-C20, C24-25 and C30-C31), CRS (C16-C18 and C28-C29) and TGV (C24-C26) are different. Organic markers were selected which can best differentiate the subtypes within source categories by considering the component levels and variations. Through a comprehensive review, we showed that it is inadvisable to directly use diagnostic ratios for source attribution, although their trends can assist in identifying influential sources.

High throughput integrated thermal characterization with non-contact optical calorimetry.

Commonly used thermal analysis tools such as calorimeter and thermal conductivity meter are separated instruments and limited by low throughput, where only one sample is examined each time. This work reports an infrared based optical calorimetry with its theoretical foundation, which is able to provide an integrated solution to characterize thermal properties of materials with high throughput. By taking time domain temperature information of spatially distributed samples, this method allows a single device (infrared camera) to determine the thermal properties of both phase change systems (melting temperature and latent heat of fusion) and non-phase change systems (thermal conductivity and heat capacity). This method further allows these thermal properties of multiple samples to be determined rapidly, remotely, and simultaneously. In this proof-of-concept experiment, the thermal properties of a panel of 16 samples including melting temperatures, latent heats of fusion, heat capacities, and thermal conductivities have been determined in 2 min with high accuracy. Given the high thermal, spatial, and temporal resolutions of the advanced infrared camera, this method has the potential to revolutionize the thermal characterization of materials by providing an integrated solution with high throughput, high sensitivity, and short analysis time.