Chlorinated and brominated polycyclic aromatic hydrocarbons (Cl/Br-PAHs) are emerging semi-volatile organic pollutants in haze-associated particulate matter (PM). Their gas–particle phase partitioning and distribution among PM fractions have not been clarified. Clarification would increase understanding of atmospheric behavior and health risks of Cl/Br-PAHs. In this study, samples of the gas phase and 4 PM phases (aerodynamic diameters (dae) > 10 μm, 2.5–10 μm, 1.0–2.5 μm, and <1.0 μm) were collected simultaneously during haze events in Beijing and analyzed. Normalized histogram distribution indicated that the Cl/Br-PAHs tended to adhere to fine particles. Over 80% of the Cl-PAHs and 70% of the Br-PAHs were associated with fine PM (dae < 2.5 μm). The gas–particle phase partitioning and PM distribution of Cl/Br-PAHs when heating of buildings was required, which was associated with haze events, were obviously different from those when heating was not required. The relationship between the logarithmic geometric mean diameters of the Cl/Br-PAH congeners and reciprocal of the temperature (1/T) suggested that low air temperatures during the heating period could lead to high proportions of Cl/Br-PAHs in the fine particles. Increased coal burning during the heating period also contributed to high Cl/Br-PAH loads in the fine particles.

Tetrabromobisphenol A (TBBPA) exists widely in river and lake sediments; it has raised growing attention in recent years as emerging contaminant due to its possible threats to the aquatic environment and human health. Using a specialized simulator, the relationships between hydrodynamic disturbances and resuspension characteristics were simulated, with an emphasis on microscopic characteristics. Furthermore, TBBPA release from sediment was studied in relation to hydrodynamic disturbances and resuspension characteristics. The results show that stronger water disturbances caused an increase in suspended solids concentration (SSC) and produced different behaviors of particle size distribution (PSD) and media diameter (D50) in the slight and large-scale resuspension situations. As for microscopic resuspension characteristics, the specific surface area (SSA) of suspended particulate matter (SPM) was very different from that of smooth particles. This difference may result from the fractal nature of the SPM. The fractal dimension (FD) of SPM was found to have a significant correlation with turbulent kinetic energy. TBBPA release into overlying water and adsorption onto SPM both increased with hydrodynamic disturbances; but the release into overlying water is more dominant. The TBBPA concentrations in SPM under different hydrodynamic conditions were significant related to SSA, indicating that SSA is a key factor affecting the TBBPA adsorption capacity of SPM. TBBPA concentrations in sediment decreased slightly with the increased hydrodynamic dispersion. Findings from this research show the importance of considering the hydrodynamic disturbance and resuspension characteristics in understanding TBBPA release behavior in aquatic environment.

To narrow the gap in our understanding of potential oxidative properties associated with Electronic Nicotine Delivery Systems (ENDS) i.e. e-cigarettes, we employed semi-quantitative methods to detect oxidant reactivity in disposable components of ENDS/e-cigarettes (batteries and cartomizers) using a fluorescein indicator. These components exhibit oxidants/reactive oxygen species reactivity similar to used conventional cigarette filters. Oxidants/reactive oxygen species reactivity in e-cigarette aerosols was also similar to oxidant reactivity in cigarette smoke. A cascade particle impactor allowed sieving of a range of particle size distributions between 0.450 and 2.02 μm in aerosols from an e-cigarette. Copper, being among these particles, is 6.1 times higher per puff than reported previously for conventional cigarette smoke. The detection of a potentially cytotoxic metal as well as oxidants from e-cigarette and its components raises concern regarding the safety of e-cigarettes use and the disposal of e-cigarette waste products into the environment.

Electronic cigarette-generated mainstream aerosols were characterized in terms of particle number concentrations and size distributions through a Condensation Particle Counter and a Fast Mobility Particle Sizer spectrometer, respectively. A thermodilution system was also used to properly sample and dilute the mainstream aerosol.Different types of electronic cigarettes, liquid flavors, liquid nicotine contents, as well as different puffing times were tested. Conventional tobacco cigarettes were also investigated.The total particle number concentration peak (for 2-s puff), averaged across the different electronic cigarette types and liquids, was measured equal to 4.39 ± 0.42 × 109 part. cm−3, then comparable to the conventional cigarette one (3.14 ± 0.61 × 109 part. cm−3). Puffing times and nicotine contents were found to influence the particle concentration, whereas no significant differences were recognized in terms of flavors and types of cigarettes used.Particle number distribution modes of the electronic cigarette-generated aerosol were in the 120–165 nm range, then similar to the conventional cigarette one.

In this study, a novel in situ sampling method was utilized to investigate the concentrations of trace metals and Pb isotope compositions among different particle size fractions in soil dust, bulk surface soil, and corresponding road dust samples collected within an urban environment. The aim of the current study was to evaluate the feasibility of using soil dust samples to determine trace metal contamination and potential risks in urban areas in comparison with related bulk surface soil and road dust. The results of total metal loadings and Pb isotope ratios revealed that soil dust is more sensitive than bulk surface soil to anthropogenic contamination in urban areas. The new in situ method is effective at collecting different particle size fractions of soil dust from the surface of urban soils, and that soil dust is a critical indicator of anthropogenic contamination and potential human exposure in urban settings.

An unbalanced nested sampling design was used to investigate the spatial scale of soil and herbicide interactions at the field scale. A hierarchical analysis of variance based on residual maximum likelihood (REML) was used to analyse the data and provide a first estimate of the variogram. Soil samples were taken at 108 locations at a range of separating distances in a 9 ha field to explore small and medium scale spatial variation. Soil organic matter content, pH, particle size distribution, microbial biomass and the degradation and sorption of the herbicide, isoproturon, were determined for each soil sample. A large proportion of the spatial variation in isoproturon degradation and sorption occurred at sampling intervals less than 60 m, however, the sampling design did not resolve the variation present at scales greater than this. A sampling interval of 20-25 m should ensure that the main spatial structures are identified for isoproturon degradation rate and sorption without too great a loss of information in this field.

Soils from Aveiro, Glasgow, Ljubljana, Sevilla and Torino have been investigated in view of their potential for translocation of potentially toxic elements (PTE) to the atmosphere. Soils were partitioned into five size fractions and Cr, Cu, Ni, Pb and Zn were measured in the fractions and the whole soil. All PTE concentrated in the <10 μm fraction. Cr and Ni concentrated also in the coarse fraction, indicating a lithogenic contribution. An accumulation factor (AF) was calculated for the <2 and <10 μm fraction. The AF values indicate that the accumulation in the finer fractions is higher where the overall contamination is lower. AF for Cr and Ni are particularly low in Glasgow and Torino. An inverse relationship was found between the AF of some metals and the percentage of <10 μm particles that could be of use in risk assessment or remediation practices.

We quantify for the first time marine aerosol properties and their differences in the offshore and remote ocean in the mid-latitude South Asian waters, low-latitude South Asian waters, and equatorial waters of the Western Pacific Ocean, based on shipboard cruise observations conducted by the Western Pacific Ocean Scientific Observation Network in winter 2018, and further investigate the effects of long-range transport of continental aerosols on the marine environment. During the overall observation period, the average number concentration of particle matter which aerodynamic diameters<2.5 μm (PM₂.₅N) was 35.1 ± 87.4 cm⁻³ and the mass concentration (PM₂.₅M) was 12.3 ± 9.1 μg/m³. The PM₂.₅N and PM₂.₅M during the continental air mass transport period were 7.2 and 1.3 times higher than those during the non-transport period (109.2 ± 169.3 cm⁻³, 15.9 ± 14.9 μg/m³), respectively. Excluding transport period, the average PM₂.₅N and PM₂.₅M are reduced by 120% and 7%. Coarse mode particle number concentration (PM₂.₅–₁₀N) and mass concentration (PM₂.₅–₁₀M) are not significantly influenced by continental air masses (only a reduction of 7% and 2%). The variation of marine aerosol concentrations in different latitudes zones is greatly influenced by continental aerosol transport. The offshore PM₂.₅M/PM₁₀M was 30%, 21%, and 22% in the mid-latitude sea of South Asia, a low-latitude sea of South Asia, and the equatorial sea, respectively. In comparison, in the remote ocean, the distribution ratio of PM₂.₅M/PM₁₀M tended to be steady (22%–23%), and the background characteristics of marine aerosols were clearly represented. The aerosol concentration decreases with the increase of wind speed during the transport period, and the wind speed reflects the scavenging effect on aerosol. In the non-transport period, the wind speed at the sea surface promotes the generation of marine aerosols, and the impact in wind speed is strongest in the PM₂.₅–PM₅ particle size range.

Assessments of antimony (Sb) and arsenic (As) contamination in sediments are reported on a wide range of different particle size fractions, including <63 μm, < 180 μm and <2 mm. Guidelines vary between jurisdictions which limits comparative assessment between contamination events and complicates ecotoxicity assessment, and almost no information exists on Sb size distribution in contaminated sediments. This study quantified and compared the size distribution of Sb and As in 11 sediments (and 2 floodplain soils) collected along 320 km of waterway contaminated by historic mining activity. Sediment particle size distribution was the primary determinant of total metalloid load in size fractions across the varying substrates of the waterway. Minerals and sorption complexes influenced metalloid particle distribution but relative importance depended on location. Arsenic concentrations were greatest in the fine <63 μm fraction across all the different river environments (7.3–189 mg kg⁻¹, or 1–26% of total sample As), attributed to fine-grained primary arsenopyrite and/or sorption of As(V) to fine solid-phases. The Sb particle size concentrations were greatest in mid-size fractions (205–903 mg kg⁻¹) in the upper catchment and up to 100 km downstream to the mid-catchment as a result of remnant Sb minerals. Antimony concentrations in the lower catchment were greatest in the <63 μm fraction (8.8–12.1 mg kg⁻¹), reflecting the increasing importance of sorption for Sb particle associations. This work demonstrates the importance of particle size analysed for assessment of sediment quality, and provides support for analysis of at least the <250 μm fraction for Sb and As when comparing pollutant distribution in events impacted by primary contamination. Analysis of the <63 μm fraction, however, provides good representation in well-dispersed contaminated sediments.

Aquatic particles and organic carbon (OC) regulate the occurrence and transport of hydrophobic organic contaminants such as polycyclic aromatic hydrocarbons (PAHs) in water-suspended particle-sediment interfaces. Conventional studies on the mechanisms regulating the relationships between PAHs and total particles/OC have ignored micro-scale regulatory factors such as particle size and OC composition. Field research in the eutrophic shallow Lake Taihu, China, revealed that the fine particle fractions 2.7–10 μm in diameter had stronger PAH adsorption capacity and significantly regulated PAH particle size distribution and water-particle partitioning. Selective PAH biodegradation by planktonic microorganisms probably significantly weakened the capacity of the coarse fractions to regulate PAHs. OC fragments at different temperature gradients had markedly different influences on the particle size distribution of PAHs. High-temperature pyrogenic OC fractions (part of black carbon) were the principal OC regulatory factors for medium-to high-molecular-weight PAHs. However, the OC fragments did not directly affect the particle distribution of low-molecular-weight PAHs. During particle deposition and burial, microbial PAH utilization and efficiency probably regulated the burial potential of various hydrophobic PAH species. Biodegradation of relatively less hydrophobic PAHs with octanol-water partition coefficients (log Kₒw) < 5.8 showed an increasing trend with decreasing PAH hydrophobicity. Biological pump action of the relatively higher hydrophobic PAH species (log Kₒw > 5.8) showed a decreasing trend with increasing PAH hydrophobicity. The discoveries of the present work further clarified the mechanisms of PAH partitioning and burial in a eutrophic shallow lake and collectively provides a valuable reference for modeling the transport and dispersal mechanisms of hydrophobic, particle-bound organic contaminants in other aquatic ecosystems.