Fraction Of Particulate Matter Research Articles

Impact of COVID-19 restrictions on the dry deposition fraction of settleable particulate matter at three industrial urban/suburban locations in northern Spain

Ninety 24-h samples of the dry deposition fraction of settleable particulate matter (DSPM) were collected at one suburban industrial site (‘EMA’) and two urban industrial sites (‘Lauredal’ and ‘Laboratory’) in the western area of Gijón (North of Spain) from December 2019 to June 2020. The levels registered point to an environmental issue that should receive close attention from environmental authorities. Before lockdown restrictions due to COVID-19 were established, all samples collected at the EMA site exceeded 300 mg·m−2·d−1 (the Spanish limit value until 2002). Large amounts of DSPM were also registered at the Lauredal and Laboratory sites, maximum levels reaching 1039.2 and 672.7 mg·m−2·d−1, respectively. Seven metals were analysed in DSPM samples: Al, Ca, Fe, K, Mg, Mn and Na. Fe reached the highest values: 2473.4, 463.4 and 293.3 mg·m−2·d−1 (EMA, Lauredal and Laboratory sites, respectively). This study quantifies the reductions in the DSPM levels registered (on average, 97.2, 73.5 and 90.5% at the EMA, Lauredal and Laboratory sites, respectively) during the lockdown, which involved the restriction of population mobility and industrial activity. The influence of wind speed and its direction were also assessed to better understand the role of these restrictions in the observed reductions. The concentrations of all the metals in the DSPM were reduced by more than 75%, on average, except for K at the Laboratory and Lauredal sites. These decreases were much higher than those found by other authors for smaller fractions of the atmospheric particulate matter (PM10, PM2.5). The findings of the present study highlight the importance of DSPM in highly industrialized urban/suburban locations and indicate the direction that legal measures might take, given the influence of anthropogenic emissions.

Sources and processes of organic aerosol in non-refractory PM1 and PM2.5 during foggy and haze episodes in an urban environment of the Yangtze River Delta, China

Organic aerosol (OA) generally accounts for a large fraction of fine particulate matter (PM2.5) in the urban atmosphere. Despite significant advances in the understanding their emission sources, transformation processes and optical properties in the submicron aerosol fraction (PM1), larger size fractions - e.g., PM2.5 - still deserve complementary investigations. In this study, we conducted a comprehensive analysis on sources, formation process and optical properties of OA in PM1 and PM2.5 under haze and foggy environments in the Yangtze River Delta (eastern China), using two aerosol chemical speciation monitors, as well as a photoacoustic extinctiometer at 870 nm. Positive matrix factorization analysis - using multilinear engine (ME2) algorithm - was conducted on PM1 and PM2.5 organic mass spectra. Four OA factors were identified, including three primary OA (POA) factors, i.e., hydrocarbon-like OA (HOA), cooking OA (COA), and biomass burning OA (BBOA), and a secondary OA (SOA) factor, i.e., oxidized oxygenated OA (OOA). An enhanced PM1-2.5 COA concentration was clearly observed during cooking peak hours, suggesting important contribution of fresh cooking emissions on large-sized particles (i.e., PM1-2.5). The oxidation state and concentration of PM2.5 HOA were higher than that in PM1, suggesting that large-sized HOA particles might be linked to oxidized POA. High contribution (44%) of large-sized OOA to non-refractory PM2.5 mass was observed during haze episodes. During foggy episodes, PM1 and PM2.5 OOA concentrations increased as a positive relationship over time, along with an exponential increase in the PM2.5-OOA to PM1-OOA ratio. Meanwhile, OOA loadings increased with the aerosol liquid water content (ALWC) during foggy episodes. Random forest cross-validation analysis also supported the important influence of ALWC on OOA variations, supporting substantial impact of aqueous process on SOA formation during haze and/or foggy episodes. Obtained results also indicated high OOA contributions (21%–36%) and low POA contributions (6%–14%) to the PM2.5 scattering coefficient during haze and foggy episodes, respectively. Finally, we could illustrate that atmospheric vertical diffusion and horizontal transport have important but different effects on the concentrations of different primary and secondary OA factors in different particle size fractions.

Influence of thermal aging and long term-aging on Ni and V content in asphalt fractions and their determination in air particulate matter from asphalt mixing plants

Ni and V can contribute to the deterioration of asphalt pavement by catalyzing the oxidation of some organic molecules present in the binder structure. In this work, the influence of the aging process on Ni and V compounds was studied by comparing the concentration of these two metals in the maltenic and asphaltenic fractions of virgin and aged asphalts. Long-term aging process was simulated by the combination of the rolling thin film oven test (RTFOT) and the SUNTEST method. The results showed that up to 56% of Ni and 53% of V were lost after aging. The greatest changes were observed for the acidic subfraction of both maltenes and asphaltenes. RTFOT/SUNTEST process was also compared to thermal aging using an extraction and collection device (DEC). All V losses were due to the emission of its volatile compounds during thermal aging. Ni losses were attributed to both UV–VIS radiation and sample heating. The presented results help to understand the behavior of both metals during asphalt aging, which has important economic value and can be useful to find solutions that delay the aging process. Ni and V were also determined in the organic fraction of air particulate matter from two asphalt mixing plants. Concentrations of Ni and V ranged from 0.42 to 0.84 ng m−3 h−1 and from 0.08 to 1.79 ng m−3 h−1, respectively, showing that the production of asphalt mixtures can contribute to the air pollution through the emission of Ni and V compounds.

Impact of Microstructure on Solar Radiation Transfer Within Sea Ice During Summer in the Arctic: A Model Sensitivity Study

The recent rapid changes in Arctic sea ice have occurred not only in ice thickness and extent, but also in the microstructure of ice. To understand the role of microstructure on partitioning of incident solar shortwave radiation within the ice and upper ocean, this study investigated the sensitivity of the optical properties of summer sea ice on ice microstructures such as the volume fraction, size, and vertical distribution of gas bubbles, brine pockets, and particulate matter (PM). The results show that gas bubbles are the predominant scatterers within sea ice. Their effects on the scattering coefficient and ice albedo are 5 and 20 times stronger respectively than the effect of brine pockets. Albedo and transmittance of ice decrease with higher concentration and larger size of PM particles. A 4-cm top layer of ice with high PM concentration (50 g/m3) results in a 10% increase in radiation absorption. The role of ice microstructure in the partitioning of radiation transfer is more important for seasonal than for multiyear ice, and more important for ponded than for snow-covered ice. Varying ice microstructure can obviously alter solar radiation transfer in the ice-ocean system, even with a constant ice thickness. Our results suggest that numerical models should take the variable microstructure of sea ice into account to improve model accuracy and to understand the interaction between internal variations in Arctic sea ice and the ocean, especially in summer.

Particulate matter and polycyclic aromatic hydrocarbon uptake in relation to leaf surface functional traits in Mediterranean evergreens: Potentials for air phytoremediation

We explored relationships between particulate matter (PM) and polycyclic aromatic hydrocarbon (PAHs) leaf concentrations, uptake rates and leaf surface functional traits in four Mediterranean evergreen trees (Chamaerops humilis, Citrus × aurantium, Magnolia grandiflora, and Quercus ilex) during a dry month. Pollutant leaf concentration at different dates and uptake rate were correlated. We quantified PM by gravimetric analysis, PAHs were extracted from intact and dewaxed leaves and analyzed by GC-MS, and cuticle thickness, number and surface of stomata (Ns and SS) and trichomes (Nt and St) were determined by optical microscopy. Infrared spectroscopy was used to investigate the leaves surfaces composition and assess esterification index (E). Studied species were characterized by unique combinations of functional traits and pollutant uptake capacities. PM10 uptake scaled positively with SS, St and upper cuticle thickness (Tc,u) across species. PM2.5 uptake scaled positively with Tc,u, and thicker cuticles were also associated with greater shares of uptake of hydrophobic PM fractions. Uptakes of different fractions of PAH were generally weakly related to different leaf functional traits, except for some correlations with E and SS. We conclude that both plant surface morphological and chemical leaf traits influence PM and PAH retention, unveiling their potential role in air phytoremediation.

Effect of nonthermal plasma with different ozone concentrations on the oxidation and removal of different components in particulate matter

Nonthermal plasma (NTP) technology can oxidize and decompose diesel particulate matter (PM) under much lower temperatures (≤200 °C) without catalyst, showing promise for potential applications. A self-made NTP generator was used to produce NTP gas that reacted with PM at a certain reaction temperature and reaction time, and the concentration of O3 in NTP was modified by adjusting the working parameters. Fourier transform infrared spectroscopy (FT-IR), thermogravimetric analysis (TGA), and gas chromatography-mass spectrometry (GC-MS) were used to analyze changes in the surface functional groups, component oxidation activity, removal effect, and the soluble organic fraction (SOF) of PM samples before and after processing. As the O3 concentration increased, the effect of NTP on PM removal strengthened. PM surface functional groups can be converted from C–OH into CO under the action of NTP at high O3 concentrations. The oxidation activity of the volatile fraction (VF) and soot in PM can be substantially improved under high O3 concentrations. Higher O3 concentrations resulted in increases in the number of oxygen-containing groups in the molecular formula of SOF and the ratio of components. This study provide a certain reference value for the strategy of removing PM pollutants from diesel engines and even the atmosphere.

Simple and efficient method to detach intact PM10 from field filters: Elements recovery assessment

Toxicity of the soluble fraction of particulate matter (PM) has been extensively evaluated, but it has also been demonstrated that insoluble aerosol species can considerably contribute to toxicological potential of PM. However, most of the procedures regarding the assessment of toxicological effects of the whole PM (soluble and insoluble species) requires targeted treatments of the sampled filters, such as the employment of organic solvents, or the application of ultrasounds. Both methods can introduce a bias in the toxicological assessment, altering PM oxidative potential and biological outcomes. In this study, we applied a non-invasive, simple and efficient method for the detachment of intact PM10 from field filters by using an electrical toothbrush, which allows obtaining a PM10 water-suspension to be used for PM toxicity assessment. The efficiency of this method was evaluated by comparing the elemental content (As, Ba, Bi, Ca, Co, Cs, Cu, Fe, Ga, K, Li, Mg, Mn, Mo, Ni, Pb, Rb, Sb, Se, Sn, Sr, Ti, Tl, U and W) obtained by brushing the filters to that measured by applying a conventional procedure to PM samples (n. 20 pairs of equivalent PM10 filters). Soluble and insoluble fractions were separately analyzed, in order to discriminate the recovery due to partial solubilization of sample from that due to detachment of insoluble particles. The high recovery percentage of elements, the very-high linear correlation coefficients and the low relative percentage differences with respect to a conventional procedure for elemental analysis of PM10 confirmed the efficiency of the toothbrush method.

Emissions of Carbonaceous Particulate Matter and Ultrafine Particles from Vehicles-A Scientific Review in a Cross-Cutting Context of Air Pollution and Climate Change.

Airborne particulate matter (PM) is a pollutant of concern not only because of its adverse effects on human health but also on visibility and the radiative budget of the atmosphere. PM can be considered as a sum of solid/liquid species covering a wide range of particle sizes with diverse chemical composition. Organic aerosols may be emitted (primary organic aerosols, POA), or formed in the atmosphere following reaction of volatile organic compounds (secondary organic aerosols, SOA), but some of these compounds may partition between the gas and aerosol phases depending upon ambient conditions. This review focuses on carbonaceous PM and gaseous precursors emitted by road traffic, including ultrafine particles (UFP) and polycyclic aromatic hydrocarbons (PAHs) that are clearly linked to the evolution and formation of carbonaceous species. Clearly, the solid fraction of PM has been reduced during the last two decades, with the implementation of after-treatment systems abating approximately 99% of primary solid particle mass concentrations. However, the role of brown carbon and its radiative effect on climate and the generation of ultrafine particles by nucleation of organic vapour during the dilution of the exhaust remain unclear phenomena and will need further investigation. The increasing role of gasoline vehicles on carbonaceous particle emissions and formation is also highlighted, particularly through the chemical and thermodynamic evolution of organic gases and their propensity to produce particles. The remaining carbon-containing particles from brakes, tyres and road wear will still be a problem even in a future of full electrification of the vehicle fleet. Some key conclusions and recommendations are also proposed to support the decision makers in view of the next regulations on vehicle emissions worldwide.

Health and Environmental Risks of Incense Smoke: Mechanistic Insights and Cumulative Evidence.

Incense burning is practiced alongside many sacred rituals across different regions of the world. Invariable constituents of incense brands are 21% (by weight) herbal and wood powder, 33% bamboo stick, 35% fragrance material, and 11% adhesive powder. Major incense-combustion outputs include particulate matter (PM), volatile organic content, and polyaromatic hydrocarbons. The relative toxicity of these products is an implicit function of particle size and incomplete combustion, which in turn vary for a specific incense brand. Lately, the attention given to the Air Quality Index by international regulatory bodies has created concern about mounting PM toxicity. The uncharacteristically small physical dimensions of these entities complicates their detection, and with no effect of gravity PM fractions rapidly contribute to oxidative stress, enhancing random biochemical reactions upon being inhaled. Incense burning generates four times the PM extent (45 mg•g−1) of cigarettes (~10 mg•g−1). Several poisonous gases, such as CO, CO2, NO2, and SO2, and the unavoidable challenge of disposing of the burnt incense ash further add to the toxicity. Taken together, these issues demonstrate that incense burning warrants prompt attention. The aim of this article is to highlight the toxicity of incense-combustion materials on the environment and human health. This discussion could be significant in framing future policy regarding ecofriendly incense manufacture and reduced usage.

Development of a new procedure for the assessment of particulate matter (PM) carbonaceous fraction on stone materials exposed to atmospheric pollution

Abstract The present study deals with the set-up and development of a new methodology to quantify the carbonaceous fraction (i.e., OC, organic carbon and EC, elemental carbon) in black crusts samples present on marble stone surfaces of historical buildings and monuments exposed to outdoor pollution. It is worth noting that OC and EC represent one of the main fractions of atmospheric particulate matter and, mainly EC, is responsible for the black colour of the crusts. The same method has been applied to resuspend known quantities of atmospheric particulate matter on marble mock-up specimens suitably realized to study the crusts’ formation process starting from known quantities of the precursors in the formation process, i.e., PM and SO2, and submitting them to an accelerated aging process.

Source identification of the elemental fraction of particulate matter using size segregated, highly time-resolved data and an optimized source apportionment approach

Source emissions with high covariance degrade the performance of multivariate models, and often highly-time resolved data is needed to accurately extract the contribution of different emissions. Here, we use highly time-resolved size segregated elemental composition data to apportion the sources of the elemental fraction of PM in Zürich (May 2019–May 2020). For data collection, we have used an ambient metals monitor, Xact 625i, equipped with a sampling inlet alternating between PM 2.5 and PM 10 . By implementing interpolation and a newly proposed uncertainty estimation methodology, it was possible to obtain and use in PMF a combined dataset of PM 2.5 and PM coarse (PM 10-2.5 ) having data from only one instrument. The combination of the inlet switching system, the instrument's high time resolution, and the use of advanced source apportionment approaches yielded improved source apportionment results in terms of the number of identified sources, as the model, additionally to the diurnal and seasonal variation of the dataset, also utilizes the variation from the size segregated data. Thirteen sources of elements were identified, i.e., sea salt (5.4%), biomass burning (7.2%), construction (4.3%), industrial (3.3%), light-duty vehicles (5.4%), Pb (0.7%), Zn (0.7%), dust (22.1%), transported dust (9.5%), sulfates (15.4%), heavy-duty vehicles (17%), railway (6.6%) and fireworks (2.4%). The Covid-19 lockdown effect in PM sources in the area was also quantified. High-intensity events disproportionally affect the PMF solution, and in many cases, they are getting discarded before analysis, removing thus valuable information from the dataset. In this study, a three-step source apportionment approach was used to get a well-resolved unmixed solution when firework data points were included in the analysis. This approach can also be used for other sources and/or events with very high contributions that distort source apportionment analysis. Optimized source apportionment techniques are necessary for effective air pollution monitoring. • Combined PM 2.5 and PM coarse elemental composition data using a single instrument. • Methodology for the estimation of the uncertainty of interpolated PM elemental composition data. • Source apportionment method for the use of data that include high-intensity events. • The effect of Covid-19 lockdown to PM source contributions. • Quantification of heavy duty & low duty vehicular emissions.

Atmospheric levels, distribution, sources, correlation with meteorological parameters and other pollutants and health risk of PAHs bound in PM2.5 and PM10 in Burgas, Bulgaria – a case study

The quality of atmospheric air of Burgas city, Bulgaria was analyzed in relation to PAHs in two particulate matter fractions – 2.5 μm and 10 μm. It was found that PAHs registered in PM10 represent entirely the ones registered in PM2.5 – an indication that the particulate PAHs in ambient air of Burgas for the sampling period are associated with the fine PM fraction. The PAH compounds with highest concentrations are mainly associated with coal combustion, diesel and gasoline vehicle and biomass burning, which is further confirmed by the calculated diagnostic ratios. The combustion-derived PAHs represent on average 86.6 ± 2.8% of total PAHs concentration. The linear regression analysis showed strong and statistically meaningful correlations between PM fractions and PAHs indicating the influence of similar local events and emission sources of pollution. PM2.5 or PM10 relationships with PAHs were significant but lower correlation coefficients were observed for low-molecular weight (LMW) PAHs in comparison to middle-molecular weight (MMW) and higher-molecular weight (HMW) PAHs, due to their lower presence in particulates and higher partition in gaseous atmospheric phase. Further significant correlations were found with wind speed, solar radiation and atmospheric pressure as well as NO2 and O3 ambient concentration. The calculated excess cancer risks are twice as much as acceptable limit.

A New Method for the Assessment of the Oxidative Potential of Both Water-Soluble and Insoluble PM

Water-soluble and insoluble fractions of airborne particulate matter (PM) exhibit different toxicological potentials and peculiar mechanisms of action in biological systems. However, most of the research on the oxidative potential (OP) of PM is focused exclusively on its water-soluble fraction, since experimental criticisms were encountered for detaching the whole PM (soluble and insoluble species) from field filters. However, to estimate the actual potential effects of PM on human health, it is essential to assess the OP of both its water-soluble and insoluble fractions. In this study, to estimate the total OP (TOP), an efficient method for the detachment of intact PM10 from field filters by using an electrical toothbrush was applied to 20 PM10 filters in order to obtain PM10 water suspensions to be used for the DCFH, AA and DTT oxidative potential assays (OPDCFH, OPAA and OPDTT). The contribution of the insoluble PM10 to the TOP was evaluated by comparing the TOP values to those obtained by applying the three OP assays to the water-soluble fraction of 20 equivalent PM10 filters. The OP of the insoluble fraction (IOP) was calculated as the difference between the TOP and the WSOP. Moreover, each PM10 sample was analyzed for the water-soluble and insoluble fractions of 10 elements (Al, Cr, Cs, Cu, Fe, Li, Ni, Rb, Sb, Sn) identified as primary elemental tracers of the main emission sources in the study area. A principal component analysis (PCA) was performed on the data obtained to identify the predominant sources for the determination of TOP, WSOP, and IOP. Results showed that water-soluble PM10 released by traffic, steel plant, and biomass burning is mainly responsible for the generation of the TOP as well as of the WSOP. This evidence gave strength to the reliability of the results from OP assays performed only on the water-soluble fraction of PM. Lastly, the IOPDCFH and IOPDTT were found to be principally determined by insoluble PM10 from mineral dust.

Association of Exposure to Particulate Matter Air Pollution With Semen Quality Among Men in China

The health effects of exposure to particulate matter (PM) on male fertility remain unclear. Although PM exposure has been linked with semen quality, the results were inconsistent. To examine the association of different size fractions of PM (<2.5 μm [PM2.5], 2.5-10 μm [PM2.5-10], and ≤10 μm [PM10]) exposure with semen quality in China. This retrospective cohort study was conducted using data on men whose wives underwent assisted reproductive technology procedures in a tertiary hospital in Shanghai, China, from January 1, 2013, to December 31, 2019. Participants were from 340 prefecture-level cities of China and were followed up from the date of their first visit until December 31, 2019. Data were analyzed from December 1, 2020, to May 15, 2021. Exposure to PM2.5, PM2.5-10, and PM10 during the entire period (0-90 days before semen ejaculation) and key periods of sperm development (0-9, 10-14, and 70-90 days before semen ejaculation). Semen quality, including sperm count, concentration, and motility. A total of 33 876 men were included in the final analysis, with a mean (SD) age of 34.1 (5.7) years and large variation of PM exposure. For example, the median exposure to PM2.5 during the entire period of sperm development was 46.05 (IQR, 34.38-61.65) μg/m3. During the entire period of sperm development, exposures to higher levels of PM were significantly associated with lower total and progressive sperm motility. For total sperm motility, an IQR increase in PM2.5 exposure was associated with an estimated effect decrease of -3.60% (95% CI, -3.93% to -3.26%); an increase in PM2.5-10 exposure, with an estimated effect decrease of -0.45% (95% CI, -0.76% to -0.14%); and an increase in PM10 exposure, with an estimated effect decrease of -2.44% (95% CI, -2.91% to -1.96%). Similar results were observed for progressive motility. An IQR increase in PM2.5 or PM10 exposures was associated with an estimated effect decrease on sperm progressive motility of -1.87% (95% CI, -2.37% to -1.36%) and -1.05% (95% CI, -1.45% to -0.64%), respectively. However, no significant associations were observed between PM exposure during the entire period of sperm development and sperm count or concentration. These findings suggest that PM exposure may adversely affect sperm motility and highlight the need to reduce ambient particulate air pollution exposure for reproductive-aged men.

The impact of stable 27Al in 26Al/10Be meteoric ratio in PM2.5 from an urban area

Meteoric 10Be and 26Al radionuclides are produced in the atmosphere, and the relationship between them has potential applications in atmospheric and climate research.In particular, the meteoric 26Al/10Be ratio has potential applications such as a chronometer for old ice, a tracer for the air exchange between the lower stratosphere and upper troposphere, production and distribution in the atmosphere of both radionuclides, and the study on solar activity. In this work, their concentrations in the fine fraction of airborne particulate matter from an urban area have been precisely determined using Accelerator Mass Spectrometry (AMS). To obtain new data about the 26Al/10Be ratio and its subsequent applications, PM2.5 in aerosol samples has been analyzed. The average ratio in samples from Mexico City was significantly higher than those previously reported by other authors. The high enrichment factors for stable Aluminum indicate that both resuspended and anthropogenic 27Al content in PM2.5 contributes significantly to the high values of 26Al in the 26Al/10Be ratio. An adjustment of 27Al concentrations from external contributions was carried out, and the corrected 26Al/10Be ratios were similar to those previously reported. In this study, a precise assessment of the possible contribution of other Aluminum sources to the aerosol samples has been carried out. Finally, the obtained ratios indicate the possibility of its future use in applications such as the dating of glaciers.

The Nature and Size Fractions of Particulate Matter Deposited on Leaves of Four Tree Species in Beijing, China

Particulate matter (PM) in different size fractions (PM0.1–2.5, PM2.5–10 and PM&gt;10) accumulation on four tree species (Populus tomentosa, Platanus acerifolia, Fraxinus chinensis, and Ginkgo biloba) at two sites with different pollution levels was examined in Beijing, China. Among the tested tree species, P. acerifolia was the most efficient species in capturing PM, followed by F. chinensis, G. biloba, and P. tomentosa. The heavily polluted site had higher PM accumulation on foliage and a higher percentage of PM0.1–2.5 and PM2.5–10. Encapsulation of PM within cuticles was observed on leaves of F. chinensis and G. biloba, which was further dominated by PM2.5. Leaf surface structure explains the considerable differences in PM accumulation among tree species. The amounts of accumulated PM (PM0.1–2.5, PM2.5–10, and PM&gt;10) increased with the increase of stomatal aperture, stomatal width, leaf length, leaf width, and stomatal density, but decreases with contact angle. Considering PM accumulation ability, leaf area index, and tolerance to pollutants in urban areas, we suggest P. acerifolia should be used more frequently in urban areas, especially in “hotspots” in city centers (e.g., roads/streets with heavy traffic loads). However, G. biloba and P. tomentosa should be installed in less polluted areas.

The botanical biofiltration of volatile organic compounds and particulate matter derived from cigarette smoke

Despite the growing use of control measures, environmental tobacco smoke (ETS) remains a significant pollutant source in indoor air in many areas of the world. Current control methods for reducing ETS exposure are inadequate to protect public health in environments where cigarettes are smoked. An alternative solution is botanical biofiltration which has previously been shown to lower concentrations of volatile organic compounds (VOCs) and particulate matter (PM) from a range of polluted air streams. This study is the first to assess the potential of a botanical biofilter with the species Spathiphyllum wallisii (Peace Lily) for the removal of cigarette-derived VOCs and all size fractions of PM. Single pass removal efficiencies of 43.26% for total VOCs and 34.37% for total suspended particles were achieved. The botanical biofilter reduced the concentrations of a range of harmful ETS chemicals including nicotine, limonene, and toluene. Evaluation of the re-emission of ETS constituents filtered by the botanical biofilter revealed no particle resuspension or off gassing. The results demonstrate the potential of botanical biofilters to reduce public ETS exposure, although further research is needed to improve upon and ensure the efficiency of these systems for practical applications.

Evaluation of Secondary Organic Aerosol (SOA) Simulations for Seoul, Korea

AbstractOrganic aerosols (OA) represent a significant fraction of total submicron particulate matter (PM1) concentrations globally, including densely populated megacities such as Seoul. However, scientific understanding of the atmospheric formation and removal processes of OA, especially for secondary organic aerosols (SOA), is still highly uncertain. In this study, we examine the characteristics of SOA formation in Seoul during spring‐summer 2016 and fall‐winter 2017/2018, using airborne and ground observations along with a 3‐D global chemical transport model, GEOS‐Chem. We use four different SOA schemes in the model, including simplified and complex volatility‐based frameworks, and evaluate them by comparing the simulations with the observations to examine how our scientific understanding embedded in each SOA scheme affects the observed biases. Our analysis of the model performance of each scheme also provides the most suitable approach in simulating SOA in a typical urban environment. Comparisons of the simulated versus observed OA concentrations show that model biases range from −72% to +118%, with considerable variability among different schemes and seasons. We find that the inclusion of semi/intermediate volatile precursors, in addition to the traditional precursors, and chemical aging (functionalization) are important factors to simulate surface SOA concentrations in Seoul. However, a comparison of observed and simulated SOA/∆CO enhancement ratios suggests that most schemes underpredict SOA aging in upper levels in the boundary layer. We also find that the simplified SOA scheme can reproduce observed OA but often shows overestimation in surface air, indicating that uncertainties exist in bottom‐up emissions and precursor parameterization in Seoul.

Overall Rate Kinetics Model for Chlorine Demand of Urban Rainfall Runoff

The built environment significantly alters the rainfall-runoff response and associated transport of particulate matter (PM), chemicals, and pathogens in the urban water cycle. Urban water sustainability requires mitigation of runoff impacts while providing a potential resource to traditional water supply sources. Chlorination for wastewater, combined sewer overflows (CSOs), and reuse waters is the most common disinfection practice to ensure public health. Chlorinated wastewater effluent is a common reclaimed water for reuse applications such irrigation and mixing with source-area runoff during wet-weather events. Chlorine demand models have been developed for source waters and wastewaters. The current study adds to this knowledge base through modeling of sodium hypochlorite demand kinetics for source-area runoff PM and also dissolved phases utilizing dissolved chemical oxygen demand (CODd). Second-order rate models of hypochlorite demand are developed for both phases, with the PM phase subdivided into three fractions on a granulometric basis. PM (suspended, settleable, and sediment) fractions exert a significant hypochlorite demand compared with the dissolved fraction. Ultimate chlorine demand translates to 36% of the CODd, of which 39% of the demand is exerted in less than 5 min, which is in the range of residence times for small manufactured unit operations that are common for best management practices (BMPs). Chlorine demand is 350 mg/g for suspended, 320 mg/g for settleable, and 650 mg/g for sediment PM.

Numerical Simulation of Topography Impact on Transport and Source Apportionment on PM2.5 in a Polluted City in Fenwei Plain

The unique energy structure, high intensity of coal production, and complex terrain, make Fenwei Plain a highly polluted region in China. In this study, we characterized the transport characteristic and sources of PM2.5 (the fraction of particulate matter ≤ 2.5 μm) in Sanmenxia, a polluted city in canyon terrain. The results showed that special topography in Sanmenxia had an important role in the transport of particulates. Sanmenxia is located between two northeast-southwest facing mountains, showing a special local circulation. The local circulation was dominated by a downslope wind at nighttime, while the cross−mountain airflow and zonal wind were dominant during the daytime in the canyon terrain. PM2.5 accumulated near Sanmenxia with the influence of downslope, zonal wind, and topography. The main regional transport paths could be summarized into an eastern path, a northern path, and a western path during the severe haze episodes. The PM2.5 source apportionment revealed by an on-line tracer-tagged of the Nested Air Quality Prediction Model System (NAQPMS) showed that the main regional sources of Sanmenxia were Yuncheng, Sanmenxia, and Weinan. The contribution to PM2.5 concentration in Sanmenxia was 39%, 25%, and 11%, respectively. The northern path had the most important impact on Sanmenxia. The results can provide scientific basis for the establishment of severe haze control in Sanmenxia and regional joint control.