Filters installed in the heating, ventilation, and air-conditioning (HVAC) systems can serve as air-cleaning and sampling devices for indoor particles. The purpose of this article is to evaluate these dual roles. An occupied home with a central HVAC system equipped with a Minimum Efficiency Reporting Value (MERV, from ASHRAE Standard 52.2) 11 filter was monitored for six weeks. Weekly airborne gravimetric and real-time sampling was performed to measure the particle size distribution and the concentration of total suspended particles (TSP), PM₁₀, PM₂.₅, PM₁, and 12 trace metals. The weekly system runtimes were intentionally changed to provide a wide range of weekly filtration volumes. The quantitative filter forensics (QFF) concentrations of particulate matter (PM) and trace metals were calculated using the analysis of the dust collected on the HVAC filter, the filtration volume, and filter in-situ efficiency. The results indicated that filtration was not influential to remove PM and trace metals as the concentrations during the weeks with continuous HVAC operation were not consistently lower than those during the other weeks. This suggests the dominance of other particle and trace metal source and loss mechanisms weakens the influence of filtration in this home. The QFF evaluation results indicated that the concentration of TSP and over half of the tested trace metals (e.g., Pb, Cd, Ni, V, Sb, K, and Sr) could be estimated by QFF within a factor of two when compared to airborne sampling results. PM₁₀, PM₂.₅, and PM₁ concentrations were significantly underestimated by QFF potentially due to the limitations of size distribution analysis by a laser diffraction particle sizer (LDPS) for the detection of <1 μm particles. Overall, while QFF was promising for TSP and some trace metals, improvement in size distribution analysis could extend the application of QFF for airborne sampling.

There is increasing concern about the environmental behaviors of microplastics (MPs), in particular fine MPs (FMPs), such as their concentrations, sources, size distributions, and fragmentation by weathering in waters. However, there is little information about size distributions of MP polymer types and their relationships to their sources. Here, we analyzed concentrations, compositions, and size distributions of 18 polymer types of MPs of >20 μm by micro-Fourier transform infrared spectroscopy with a novel pretreatment method in surface waters at five sites from the headwaters to the mouth of a Japanese river, and in influent and effluent from a sewage treatment plant (STP). The microplastic concentrations ranged from 300 to 1240 particles/m³ in surface waters. Cluster analysis identified two primary sources of MPs: residential wastewater at the headwater site and non-point sources from urban areas at downstream sites; concentrations of chemical contaminants from STPs were much higher at the downstream sites. The median particle sizes (D₅₀) of MPs increased in urban areas at the downstream sites and were larger than those in influent and effluent. These results imply the release of larger MPs from non-point sources in urban areas. The size distributions of each polymer and all MPs could be fitted significantly to the Weibull distribution function. Values of D₅₀, shape parameters, and scale parameters estimated from the functions were useful indicators for evaluating size distributions in detail. A significant positive correlation of D₅₀ with the tensile strengths of virgin polymers among 13 dominant polymers detected in the surface water suggests that the fragmentation properties of each polymer are influenced by its physical strength. Multidimensional analysis with concentrations, polymeric compositions, and size distributions of MPs, including FMPs, could provide useful information about their sources and their environmental behaviors.

Black carbon (BC) is the most important aerosol light-absorbing component, and its effect on radiation forcing is determined by its microphysical properties. In this study, two microphysical parameters of refractory BC (rBC), namely, size distribution and mixing state, in urban Beijing from 2013 to 2019 were investigated to understand the effects of source changes over the past years. The mass equivalent diameter of rBC (Dc) exhibited bimodal lognormal distributions in all seasons, with the major modes accounting for most (>85%) of the rBC masses. The mass median diameter (MMD) was obviously larger in winter (209 nm) than in summer (167 nm) likely due to the contribution of more rBC with larger Dc from solid fuel combustion and enhanced coagulation of rBC in polluted winter. More rBC particles were thickly coated in winter, with the number fraction of thickly coated rBC (fcₒₐₜBC) ranging within 29%–48% compared with that of 12%–14% in summer. However, no evidential increase in BC light-absorption capability was observed in winter. This finding was likely related to the lower absorption efficiency of larger rBC in winter, which partly offset the coating-induced light enhancement. Two stage of decreases in MMD and fcₒₐₜBC were observed, accompanied with a persistent decrease in rBC loading, thereby reflecting the discrepant effects of source control measures on rBC loading and physical properties. The control measures in the earlier stage before 2016 was more efficient to reduce the rBC loading but slightly influenced the microphysical properties of rBC. As of 2016, the reduction in rBC concentration slowed down because of its low atmospheric loading. However, rBC showed a more obvious decrease in its core size and became less coated. The decrease in fcₒₐₜBC may have weakened the BC absorption and accelerated the decrease in light absorption resulting from the reduction in rBC loading.