Alveolar and tracheobronchial-deposited submicrometer particle number and surface area data received by different age groups in Australia are shown. Activity patterns were combined with microenvironmental data through a Monte Carlo method. Particle number distributions for the most significant microenvironments were obtained from our measurement survey data and people activity pattern data from the Australian Human Activity Pattern Survey were used. Daily alveolar particle number (surface area) dose received by all age groups was equal to 3.0 × 10¹⁰ particles (4.5 × 10² mm²), varying slightly between males and females. In contrast to gender, the lifestyle was found to significantly affect the daily dose, with highest depositions characterizing adults. The main contribution was due to indoor microenvironments. Finally a comparison between Italian and Australian people in terms of received particle dose was reported; it shows that different cooking styles can affect dose levels: higher doses were received by Italians, mainly due to their particular cooking activity.

On-road emissions are a major contributor to rising concentrations of atmospheric greenhouse gases. In this study, we applied a downscaling methodology based on commonly available spatial parameters to model on-road CO₂ emissions at the 1 × 1 km scale for the Boston, MA region and tested our approach with surface-level CO₂ observations. Using two previously constructed emissions inventories with differing spatial patterns and underlying data sources, we developed regression models based on impervious surface area and volume-weighted road density that could be scaled to any resolution. We found that the models accurately reflected the inventories at their original scales (R² = 0.63 for both models) and exhibited a strong relationship with observed CO₂ mixing ratios when downscaled across the region. Moreover, the improved spatial agreement of the models over the original inventories confirmed that either product represents a viable basis for downscaling in other metropolitan regions, even with limited data.

The occupational exposure to airborne particles and other pollutants in a high performance jet engine airport was investigated. Three spatial scales were considered: i) a downwind receptor site, ii) close to the airstrip, iii) personal monitoring. Particle number, surface area, mass concentrations and distributions were measured as well as inorganic and organic fractions, ionic fractions and Polycyclic Aromatic Hydrocarbons. Particle number distribution measured at a receptor site presents a mode of 80 nm and an average total concentration of 6.5 × 10³ part. cm⁻³; the chemical analysis shows that all the elements may be attributed to long-range transport from the sea. Particle number concentrations in the proximity of the airstrip show short term peaks during the working day mainly related to takeoff, landing and pre-flight operations of jet engines. Personal exposure of workers highlights a median number concentration of 2.5 × 10⁴ part. cm⁻³ and 1.7 × 10⁴ part. cm⁻³ for crew chief and hangar operator.

The HERMES model-predicted Hg concentrations and fluxes in Lake Ontario were based on twelve lake and drainage basin variables (i.e., water temperature, precipitation rate, air Hg, surface area, mean depth, water volume, water inflow rate, inflow water Hg, inflow and lake suspended particulate matter, air–water and water–air mass transfer coefficients, and sedimentation rate). The HERMES model-predicted Hg water and surface sediment concentrations were found to be significantly correlated (±20%) with measured values (r² = 0.94, p < 0.0001, n = 13) and mechanistic model predictions (LOTOX2-Hg, r² = 0.95, p < 0.0001, n = 10). The predictive capacity of HERMES was previously tested on smaller (≤1 km²) lakes in Nova Scotia and Ontario, Canada (i.e., water and sediment Hg concentrations were ±15% of measured data). Results suggest that HERMES could be applicable to a broad range of lake sizes. Uncertainty analyses on HERMES model input variables indicated a larger atmospheric Hg contribution for Lake Ontario when compared to previous predictions for smaller lakes.

We quantify and compare different measures of potential propagule pressure (PPP) of aquatic invasive species (AIS) from commercial vessels in Canada. We used ship arrivals and ballast water discharge volumes as proxies for PPP from ballast water organisms, and wetted surface area (WSA) as a proxy for hull fouling PPP, to determine their relative contributions to total PPP. For three regions studied, PPP proxies correlated significantly across ports and some vessel categories. Relative contributions of ship arrivals, ballast discharge, and WSAs to PPP, evidenced by non-significant correlations across these measures, varied across regions, ports, vessel types, and seasons. Flow-through (dominant on east and west coasts) and empty-refill (in Great Lakes-St. Lawrence region) were the major ballast water exchange methods employed by the vessels surveyed. These methods have different biological efficacy for AIS removal, influencing PPP. Our study illustrates benefits and limitations of using different PPP proxies to estimate invasion risk.

The present work focused on treatment of eosin (EO) by photocatalysis (PC) combined with electrocatalysis (EC) process. Bismuth oxychloride/titanium dioxide (BiOCl/TiO₂) hybrid particles, which were used as new heterogeneous photocatalysts, were exploited in a reverse microemulsion approach and were characterized by XRD, UV–Vis diffuse spectra, BET, and SEM technologies. All degradation experiments were performed using a self-assemble experimental setup, in which PC and EC could be carried out simultaneously or individually. The results indicated that BiOCl/TiO₂ showed enhanced photocatalytic performance under UV irradiation, and 50% BiOCl/TiO₂ exhibited the best photoactivity due to its high degree of crystallization, the mesoporous structure and corresponding large special surface area, improved absorption ability in UV region, and the heterojunction formed between two coupling particles. The combined degradation process displayed synergistic effect on the degradation of EO owing to the generation of H₂O₂ at graphite cathode. The parameters such as, pH, reaction current, and initial concentration of EO were monitored in order to optimize the operating conditions. Pseudo-first-order kinetics was proposed and roughly fitted the combined degradation of EO. The combined system in this work suggested a new research idea for the degradation of dye wastewater.

As global mercury emissions from coal fire power plants increase with the continuing rise of coal consumption, mercury capture methods are being developed to prevent mercury’s escape into the atmosphere. Titanium dioxide (TiO₂) in the presence of ultra violet light (UV-A; λ ₘₐₓ ∼360 nm) and oxygen will capture mercury as the solid product HgO₍ₛ₎. Testing the effects of TiO₂ in the presence of other pollutants has so far been limited. We have performed kinetic and product studies of mercury adsorption in the presence of the gaseous flue co-pollutant NO₂₍g₎. We extensively studied the gas-phase reaction of NO₂(g) with Hg ₍g₎ ⁰ . We compared the gas-phase reaction to the same reaction performed in the presence of thin TiO₂ particle surfaces from 0 to 100 % relative humidity. The second-order rate constant was measured to be k = (3.5 ± 0.5) × 10⁻³⁵ cm⁶ molecules⁻² s⁻¹, independent of the presence of titania or the total surface area available for adsorption. Exposure of NO₂₍g₎ to titania surfaces that were already saturated in captured mercury (HgO₍ₛ₎) increased total mercury uptake onto the surface. We discuss the implications of this study to the capture of mercury emissions prior to release to the atmosphere.

We examined the sorption of heavy metals and polycyclic aromatic hydrocarbons (PAHs) to surface-oxidized activated carbon (AC) and its effect on the distribution of those compounds in sediments. Created surface oxygen groups on AC enhanced the sorption of copper, which is superior in sorption competition, in the marine sediments. In case of cadmium, aqueous chemistry altered by AC addition, such as pH, has greater impact on the bioavailability according to the result of a sequential extraction combined with the pore water concentration measurements. Oxidized AC exhibited 2.3 times more adsorption of reduced bioavailable copper while 23% of bioavailable cadmium was adsorbed onto unmodified AC. No significant changes in BET surface area, pore volume, and AC/water distribution coefficient (K AC) of PAHs were observed with surface-oxidized AC. The largest difference in K AC after the oxidation was only 0.14 log unit. Consequently, freely dissolved aqueous concentrations of PAHs were reduced by more than 96% for all tested ACs in a week despite the increased Cu sorption on AC. This indicates that enhanced metal sorption by surface oxidation of AC is less significant in controlling bioavailability of PAHs in sediments than particle size or sorbent dose.

An effective adsorbent for the removal of heavy metals was manufactured by immobilization of jujube powder. The adsorptions of Cd, Zn and Cu from aqueous solutions by jujube complex beads (Type 1 and Type 2) were studied in a batch adsorption system. The adsorption data were fitted well with the Langmuir isotherm models. The adsorption capacities (β) for Cd, Zn and Cu were 4.23, 2.93 and 3.64 mg/g in Type 1 and 1.24, 0.70 and 1.35 mg/g in Type 2 beads. The removal efficiencies of the Type 2 beads, with a larger unit surface area, were lower than those of the Type 1 due to part of the casein or cyclic AMP being destroyed during the drying process of the Type 1. These values for Type 1 beads were higher than those of all other adsorbents for each heavy metal. A comparison of the kinetic models on the overall adsorption rate showed that the adsorption system was best described by pseudo-first-order kinetics. The removal efficiencies of Cd, Zn and Cu exhibited similar tendencies to those observed in the equilibrium tests. This indicates that the jujube complex beads developed in this study can be used as promising adsorbents for the removal of heavy metals from wastewater.

Nanoparticles (NPs) are emerging as a new type of contaminant in water and wastewater. The fate of titanium dioxide nanoparticles (TiO₂NPs) in a granular activated carbon (GAC) adsorber and their impact on the removal of trichloroethylene (TCE) was investigated. Key parameters governing the TiO₂NP–GAC interaction such as specific surface area (SSA), zeta potential, and the TiO₂NP particle size distribution (PSD) were determined. The impact of TiO₂NPs on TCE adsorption on GAC was tested by conducting TCE adsorption isotherm, kinetic, and column breakthrough studies in the presence and absence of TiO₂NPs. SSA and pore size distribution of the virgin and spent GAC were obtained. The fate and transport of the TiO₂NPs in the GAC fixed bed and their impact on TCE adsorption were found to be a function of their zeta potential, concentration, PSD, and the nature of their aggregation. The TiO₂NPs under investigation are not stable in water and rapidly form larger aggregates. Due to the fast adsorption kinetics of TCE, the isotherm and kinetic studies found no effect from TiO₂NPs. However, TiO₂NPs attached to GAC and led to a reduction in the amount of TCE adsorbed during the breakthrough experiments suggesting a preloading pore blockage phenomenon. The analysis of the used GAC confirmed the pore blockage and SSA reduction.