ABSTRACT
Microplastics (MPs) in the air and indoor environments are of growing concern and have led to increased testing for MPs. This study draws attention to the quality and quantitative measures of MP studies by conducting laboratory experiments (on solutions, filters, and blank samples) that were rarely or were not adopted in the airborne and indoor MP literature. Experiments have been conducted to identify contaminations that may come from experimental procedures while determining MPs in the air samples. MPs in different matrices during experiments were counted and categorized by their shapes. Chemical characterization was performed by Raman Spectroscopy. Results showed that laminar flow is the best option over a fume hood or standard laboratory environment for detecting air MPs to reduce blank levels. Blue-green and Black-Grey were the dominant colors; fiber was the predominant type of MPs seen, and most of them fall under the size range from (1-1000 µm) in different indoor environments and blanks. Common MPs seen were PP, PVA, PTFE, PVC, and HDPE. Thermal treatment of fresh unused filters at 450 °C for 4 h was effective as it reduced the MP count by 50%. Working solutions are mainly contaminated, and their pre-filtration is essential. The average deposition of MPs in blank samples during seven days was around 55 MPs. There is an urgent need for studies on developing quality control and quality assurance of airborne and indoor MPs. Hence, a standard protocol needs to be accepted; by harmonizing procedures, comparable results can be found, uncovering the correct levels of MP contamination, as required for risk assessment.
Subject(s)
Microplastics , Plastics , Environmental Monitoring , Filtration , GasesABSTRACT
Trace metals, as constituents of ambient air, can have impacts on human and environmental health. The Global Atmospheric Passive Sampling (GAPS) and GAPS Megacities (GAPS-MC) networks investigated trace metals in the air at 51 global locations by deploying polyurethane foam disk passive air samplers (PUF-PAS) for periods of 3-12 months. Aluminum and iron exhibited the highest concentrations in air (xÌ = 3400 and 4630 ng/m3, respectively), with notably elevated values at a rural site in Argentina thought to be impacted by resuspended soil. Urban sites had the highest levels of toxic Pb and Cd, with enrichment factors suggesting primarily anthropogenic influences. High levels of As at rural sites were also observed. Elevated trace metal concentrations in cities are associated with local emissions and higher PM2.5 and PM10 concentrations. Brake and tire wear-associated metals Sb, Cu, and Zn are significantly correlated and elevated at urban locations relative to those at background sites. These data demonstrate the versatility of PUF-PAS for measuring trace metals and other particle-associated pollutants in ambient air in a cost-effective and simple manner. The data presented here will serve as a global baseline for assessing future changes in ambient air associated with industrialization, urbanization, and population growth.
ABSTRACT
The pandemic of COVID-19 currently shadows the world; the whole earth has been on an unprecedented lockdown. Social distancing among people interrupted domestic and international air traffic, suspended industrial productions and economic activities, and had various far-reaching and undetermined implications on air quality. Improvement in air quality has been reported in many cities during the lockdown. On March 22, 2020, the Turkish government enforced strict lockdown measures to reduce coronavirus disease transmission. This lockdown had a significant impact on the movement of people within the country, which resulted in a major drop in worldwide commercial activities. During this period, university campuses were emptied due to the transition to distance education. In this study, various air pollutants sulfur dioxide (SO2), nitrogen dioxide (NO2), ozone (O3), fine particulate matter (PM2.5), total bacteria, and total fungi were measured in different indoor environments at Eskisehir Technical University Campus in Eskisehir, Turkey during COVID-19 lock down period. Also, to calculate the indoor and outdoor ratios (I/O) of the pollutants, simultaneous outdoor measurements were also carried out. The average indoor SO2, NO2, O3, and PM2.5 concentrations in different indoor environments ranged between 2.10 and 54.58, 1.36-30.89, 12.01-39.05, and 21-94 µg/m3, respectively. The total number of bacteria and fungi ranged between 21.83-514.15 and 13.10-83.36 CFU/m3, respectively. Our study intends to give a glimpse to quantify the impact of a pandemic on air quality in different indoor environments in a university campus in Eskisehir, Turkey and calls for follow-up studies. Indoor concentrations were evaluated together with outdoor concentrations. In general, it can be said that the calculated I/O ratios for SO2, NO2, O3, bacteria, and fungi were less than 1 in most indoor environments.
ABSTRACT
The gaseous and PM10 emissions of a piston-engine aircraft during ground operations at different engine states (six engine speed points and three air/fuel mixtures) representing certain flight phases were concurrently measured from the exhaust duct. PM10 emissions were sampled on a 47 mm-diameter polytetrafluoroethylene (PTFE) filter in order to be analyzed with an inductively coupled plasma mass spectrometry (ICP-MS/MS) to identify the presence and level of forty-eight elements. The most abundant element is found to be Pb (med = 4.6 × 106 ng m-3), which is 40 times the second most abundant element, Na (med = 1.1 × 105 ng m-3). The filters used for sampling exhaust gases tend to lighten with an increase in engine speed and leaning of the fuel mixture. The average of measured PM mass concentrations at all engine speeds were calculated to be 27.7 mg m-3 (full-rich) > 26.7 mg m-3 (best-power) > 24.7 mg m-3 (best-economy). The total mass of the trace elements constitutes an average of 24.1 ± 12.8% of the mass of PM. Electron microscope analyses suggest that the particles enriched by Al tend to agglomerate in a needle-shaped structure.
Subject(s)
Air Pollutants , Trace Elements , Air Pollutants/analysis , Aircraft , Gases , Particulate Matter/analysis , Tandem Mass Spectrometry , Vehicle Emissions/analysisABSTRACT
Abstract: Plastics are an integral but largely inconspicuous part of daily human routines. The present review paper uses cross-disciplinary scientific literature to examine and assess the possible effects of nanoplastics (NPs) concerning microplastics (MPs) on human health and summarizes crucial areas for future research. Although research on the nature and consequences of MPs has seen a substantial rise, only limited studies have concentrated on the atmospheric nanosized polymeric particles. However, due to the intrinsic technological complications in separating and computing them, their existence has been difficult to determine correctly. There is a consensus that these are not only existing in the environment but can get directly released or as the outcome of weathering of larger fragments, and it is believed to be that combustion can be the tertiary source of polymeric particles. NPs can have harmful consequences on human health, and their exposure may happen via ingestion, inhalation, or absorption by the skin. The atmospheric fallout of micro (nano) plastics may be responsible for contaminating the environment. Apart from this, different drivers affect the concentration of micro (nano) plastics in every environment compartment like wind, water currents, vectors, soil erosion, run-off, etc. Their high specific surface for the sorption of organic pollutions and toxic heavy metals and possible transfer between organisms at different nutrient levels make the study of NPs an urgent priority. These NPs could potentially cause physical damage by the particles themselves and biological stress by NPs alone or by leaching additives. However, there is minimal understanding of the occurrence, distribution, abundance, and fate of NPs in the environment, partially due to the lack of suitable techniques for separating and identifying NPs from complex environmental matrices. Highlights: Micro (nano) plastics generated may reach the soil, water, and atmospheric compartments.Atmospheric currents serve as a way to transport, leading to micro (nano) plastics pollution.Exposure to micro (nano) plastics may happen via ingestion, inhalation, or absorption by the skin.Nanoplastics may be environmentally more harmful than other plastic particles; the focus should be on defining the exact size range.Visual classification of micro (nano) plastics is poor in reliability and may also contribute to microplastics being misidentified.
ABSTRACT
Daily gas and particle phase samples were collected during winter and summer seasons in Bolu, which is located in the high altitude Western Black Sea Region of Turkey. Samples were analyzed to determine the concentrations of polychlorinated biphenyls (PCBs) and organochlorine pesticides (OCPs). Concentrations of endosulfan sulfate and methoxychlor were found to be highest in the summer and winter periods, respectively. The measured average concentration of endrin was considerably higher (10-50 fold) than the values reported in the literature for similar sites. The agricultural areas located to the south, south-east and south-west of the sampling point were identified as source regions. PCBs were found predominantly in the gas phase in both seasons and 3-chlorinated biphenyls were found to be abundant in the winter period, due to pollutants transported from the city centre and a waste incineration plant by southerly and easterly winds. The concentrations of PCB-180 and PCB-194 were found to be higher than values reported in the literature. The correlation between atmospheric concentrations and temperature was obtained by using Clausius-Clapeyron (CC) plots. The CC plots for most of the OCPs showed shallow negative slopes with low r(2) values, which might be due to the presence of local sources, i.e., agricultural areas around the sampling site and the dominance of evaporation. The CC plots showed steep positive slopes for most of the PCB compounds. Most of the PCB compounds were carried from the ongoing local sources.
Subject(s)
Air Pollutants/analysis , Hydrocarbons, Chlorinated/analysis , Particulate Matter/analysis , Pesticides/analysis , Polychlorinated Biphenyls/analysis , Air Pollution/statistics & numerical data , Altitude , Atmosphere/chemistry , Black Sea , Environmental Monitoring , Seasons , TurkeyABSTRACT
Ambient gas and particle phase samples were collected during two sampling periods from a residential area of an industrialized city, Kocaeli, Turkey. The sampling occurred during winter months when structures were being heated, and summer months when structures were not being heated. Σ(13)PAH (gas + particle) concentrations ranged between 6.2 ng m(-3) (DahA) and 98.6 ng m(-3) (Phe) in the heating (winter) period and 3.0 ng m(-3) (BaA) and 35.1 ng m(-3) (Phe) in the non-heating (summer) period. Phe, Flt and Pyr were found to be at high concentrations in both sampling periods. Winter time to summer time concentration ratios for individual ambient PAH concentration ratios ranged between 1.2 (DahA) and 17.5 (Flu), indicating the effect of the emissions from residential heating on measured concentrations of PAHs, but great industrial plants and the only incinerator facility of Turkey are other important pollution sources around the city. Temperature dependence of gas phase PAHs was investigated using the Clausius-Clapeyron equation. A high slope obtained (5069.7) indicated the effect of the local sources on measured gas phase PAHs. Correlation of the supercooled vapor pressure (P) with the gas particle partitioning coefficient (K(p)) and particle phase fraction was also evaluated. The relationship between the meteorological parameters and individual PAH (gas + particle) concentrations was investigated further by multiple linear regression analysis. It was found that the temperature had a significant effect on all of the measured PAH concentrations, while the effects of the wind speed and direction were not significant on the individual PAHs. On the other hand, PAH concentrations showed a strong linear relationship with the ventilation coefficient (VC) which showed the influence of local sources on measured PAHs. Benzo[a]pyrene toxic equivalent (BaP(eq.)) concentrations were used for health risk assessment purposes. The winter period risk level (2.92 × 10(-3)) due to the respiratory exposure to PAHs was found to be almost 3 times higher than in the summer period (1.15 × 10(-3)).
Subject(s)
Air Pollutants/analysis , Atmosphere/chemistry , Polycyclic Aromatic Hydrocarbons/analysis , Air Pollution/statistics & numerical data , Cities , Environmental Monitoring , Health Status , Humans , Industry , Risk Assessment , Seasons , TurkeyABSTRACT
Personal exposure to volatile organic compounds (VOCs) is mainly associated with indoor exposures; however, elevated short-term exposures may also occur during ambient activities. Handheld two-stroke gasoline-powered engines have widespread use in agriculture, but so far, no studies have been conducted on the potential health risks due to the inhalation of emitted VOCs. A one-week passive sampling has been conducted on olive farm workers during the harvesting season to monitor personal exposure levels to VOCs. The first group of workers was selected to represent the contribution of gasoline-powered shaker to daily personal VOC exposures, and one another group of workers was selected as the control, whose have not been using the device. Higher concentrations of 1-pentene, n-hexane, isopentane, n-pentene, and toluene were observed in personal samples collected from machine operators. Personal exposure concentrations of a total of 45 monitored VOCs varied between 29.2 ± 10.7 and 3733.4 ± 3300.1 µg m-3 among 20 volunteer workers. Estimated carcinogenic risks were between the acceptable levels of 10-4 and 10-6 for all workers. All individual chronic HQs and HIs (as the sum of individual HQs) were below the benchmark value of 1 for regular workers in 3 different sampling sites, whereas HI values in both acute (short term) and chronic exposure scenarios were exceeded 1 for shaker machine operators. This represented potential non-carcinogenic health hazards for exposed shaker operators, along with elevated VOCs.
Subject(s)
Air Pollutants , Olea , Stroke , Volatile Organic Compounds , Humans , Volatile Organic Compounds/analysis , Air Pollutants/analysis , Gasoline , Pentanes , Farmers , Toluene , Alkenes , Environmental MonitoringABSTRACT
The precise characterization of the elemental composition of cereals and cereal products is becoming crucial to assess their nutritional values, geographical labeling, and also toxicological profile. Inductively coupled plasma-mass spectrometry (ICP-MS) has become popular for the elemental analysis of foods in recent years. Analytical performance of the inductively coupled plasma-tandem mass spectrometry (ICP-MS/MS) is improved with a reaction/collision cell that provides an interference-free analysis of most of the elements including phosphorus and sulfur. In this study, an analytical method was optimized for the quantification of 57 elements using ICP-MS/MS technique and validated for 25 elements that were available in certified reference materials (CRMs). Then, the mineral contents of semolina samples obtained from the durum wheat (Triticum durum) cultivars were analyzed according to the validation procedure. Recoveries of the elements were found in the range of 92-108% for the digested CRM. The method was robust for all elements and the results indicated good precision for the analytical method. The inter- and intra-day precision values were found below 5%, and in the range of 0.11-3.31% and 0.09-4.51%, respectively. Analyzed elements showed significant variability among the semolina samples. The variety and growing conditions might have influences on the elemental composition of semolina samples.
Subject(s)
Trace Elements , Triticum , Edible Grain/chemistry , Phosphorus/analysis , Spectrum Analysis , Tandem Mass Spectrometry , Trace Elements/analysisABSTRACT
Atmospheric pollutants including ozone, nitrogen dioxide, sulfur dioxide, and BTEX (benzene, toluene, ethylbenzene, and xylenes) compounds were evaluated concerning their spatial distribution, temporal variation, and health risk factor. Bolu plateau where sampling was performed has a densely populated city center, semi-rural areas, and forested areas. Additionally, the ozone formation potentials of BTEXs were calculated, and toluene was found to be the most important compound in ground level ozone formation. The spatial distribution of BTEXs and nitrogen dioxide pollution maps showed that their concentrations were higher around the major roads and city center, while rural-forested areas were found to be rich in ozone. BTEXs and nitrogen dioxide were found to have higher atmospheric concentrations in winter. That was mostly related to the source strength and low mixing height during that season. The average toluene to benzene ratios demonstrated that there was a significant influence of traffic emissions in the region. Although there was no significant change in sulfur dioxide concentrations in the summer and winter seasons of 2017, the differences in the spatial distribution showed that seasonal sources such as domestic heating and intensive outdoor barbecue cooking were effective in the atmospheric presence of this pollutant. The lifetime cancer risk through inhalation of benzene was found to be comparable with the limit value (1 × 10-6) recommended by USEPA. On the other hand, hazard ratios for BTEXs were found at an acceptable level for different outdoor environments (villages, roadside, and city center) for both seasons.
Subject(s)
Air Pollutants , Ozone , Air Pollutants/analysis , Benzene/analysis , Benzene Derivatives/analysis , Environmental Monitoring , Nitrogen Dioxide , Ozone/analysis , Sulfur Dioxide , Toluene/analysis , Turkey , Xylenes/analysisABSTRACT
Coronavirus disease 2019 (COVID-19) is caused by the SARS-CoV-2 virus and has been affecting the world since the end of 2019. The disease led to significant mortality and morbidity in Turkey, since the first case was reported on March 11th, 2020. Studies suggest a positive association between air pollution and SARS-CoV-2 infection. The aim of the present study was to investigate the role of ambient particulate matters (PM), as potential carriers for SARS-CoV-2. Ambient PM samples in various size ranges were collected from 13 sites including urban and urban-background locations and hospital gardens in 10 cities across Turkey between 13th of May and 14th of June 2020 to investigate the possible presence of SARS-CoV-2 RNA on ambient PM. A total of 203 daily samples (TSP, n = 80; PM2.5, n = 33; PM2.5-10, n = 23; PM10µm, n = 19; and 6 size segregated PM, n = 48) were collected using various samplers. The N1 gene and RdRP gene expressions were analyzed for the presence of SARS-CoV-2, as suggested by the Centers for Disease Control and Prevention (CDC). According to real time (RT)-PCR and three-dimensional (3D) digital (d) PCR analysis, dual RdRP and N1 gene positivity were detected in 20 (9.8%) samples. Ambient PM-bound SARS-CoV-2 was analyzed quantitatively and the air concentrations of the virus ranged from 0.1 copies/m3 to 23 copies/m3. The highest percentages of virus detection on PM samples were from hospital gardens in Tekirdag, Zonguldak, and Istanbul, especially in PM2.5 mode. Findings of this study have suggested that SARS-CoV-2 may be transported by ambient particles, especially at sites close to the infection hot-spots. However, whether this has an impact on the spread of the virus infection remains to be determined.
Subject(s)
Air Pollutants , COVID-19 , Air Pollutants/analysis , Cities , Humans , Particulate Matter/analysis , RNA, Viral , SARS-CoV-2 , Turkey/epidemiologyABSTRACT
An analytical method was optimized for quantification of 67 elements including P, S and Si in size-segregated atmospheric particulate matter (PM) samples by Inductively Coupled Plasma-Tandem Mass Spectrometry (ICP-MS/MS). The analytical performance of ICP-MS/MS system using O2 as reaction gas and He as collision gas into the octopole collision/reaction cell (CRC) by mass shift and on mass using single MS modes were evaluated to enhance interference-free analysis. Satisfactory recoveries of elements in the range of 71.5%⯱â¯3.4% (Ca) and 110.9%⯱â¯13.1% (Si) were obtained by dissolving and analyzing certified reference material (CRM - NIST 1648a, urban dust). Elemental S in PM samples with high recovery (96.6%⯱â¯3.9%) was reported for the first time by using an ICP-MS/MS technique. ICP-MS/MS is a very powerful technique and provides interference-free detection of elements in PM samples.
ABSTRACT
A tailor-made diffusive sampler has been developed for the determination of nitrogen dioxide (NO2), sulfur dioxide (SO2) and ozone (O3) concentrations with a performance evaluation of the sampler being carried out under field and laboratory conditions. The most important characteristics of the sampler design is that simultaneous sampling of the three pollutants can be performed in one sampler. All the parts of the diffusive sampler are reusable after cleaning. These properties provide important advantages in terms of cost and practicality. Two alternative samplers, having long and short diffusion paths, have been designed. Extensive validation studies, including detection limit, precision, accuracy, recovery, shelf life, storage stability, comparison with commercial diffusive samplers, and the effects of shelter use were conducted in accordance with European Standards (EN). According to the validation results, all of the parameters evaluated for the diffusive sampler (for both long and short diffusion path designs) comply with the related standards and the sampler is expected to play an important role in the widespread monitoring of inorganic pollutants, since it is cheap, easy to use and deliverable within the country.
ABSTRACT
Kütahya city, a thermal power plant (TPPs) affected region of Turkey, has serious air quality problems like similar industrial regions of the world due to the emissions from three closely-located coal-fired TPPs, residential coal combustion along with the contribution of several industrial stacks. The organic chemical speciation of ambient size-segregated particulate matter (PM) was investigated during two seasons at two sites with different pollution characteristics (urban and rural). The ambient PM was collected using a high volume cascade impactor, with 6 stages: PM>10.2, PM10.2-4.2, PM4.2-2.1, PM2.1-1.3, PM1.3-0.69 and PM<0.69. Collected PM samples were extracted with organic solvents and the organic composition (Polycyclic aromatic hydrocarbons (PAHs), n-alkanes and carboxylic acids) was determined by GC-MS. Sources of the organic species were assessed using molecular PAH diagnostic ratios, carbon preference index and wax percentages. More than 70% of the PM-bound PAHs were quantified in submicron particles. Similarly, 34-42% of n-alkanes and approximately 30% of the carboxylic acids were found on the smallest particles. The main sources of the PM-bound organic species were considered as the anthropogenic emissions such as coal and biomass combustion and also vehicular emissions rather than the biogenic sources. Considerably high cancer risk levels were obtained through inhalation of PAHs. Seasonal variations and size distributions of the carboxylic acids and levoglucosan were also evaluated. Polar organic compound concentrations were higher in the summer period at both locations probably due to the higher sunlight intensity and temperature favoring their photochemical formation.
Subject(s)
Air Pollutants/analysis , Polycyclic Aromatic Hydrocarbons/analysis , Cities , Environmental Monitoring , Organic Chemicals/analysis , Particle Size , Particulate Matter/analysis , Photochemical Processes , Power Plants , Seasons , TurkeyABSTRACT
A pilot study was initiated in 2018 under the Global Atmospheric Passive Sampling (GAPS) Network named GAPS-Megacities. This study included 20 megacities/major cities across the globe with the goal of better understanding and comparing ambient air levels of persistent organic pollutants and other chemicals of emerging concern, to which humans residing in large cities are exposed. The first results from the initial period of sampling are reported for 19 cities for several classes of flame retardants (FRs) including organophosphate esters (OPEs), polybrominated diphenyl ethers (PBDEs), and halogenated flame retardants (HFRs) including new flame retardants (NFRs), tetrabromobisphenol A (TBBPA) and hexabromocyclododecane (HBCDD). The two cities, New York (USA) and London (UK) stood out with â¼3.5 to 30 times higher total FR concentrations as compared to other major cities, with total concentrations of OPEs of 15,100 and 14,100 pg/m3, respectively. Atmospheric concentrations of OPEs significantly dominated the FR profile at all sites, with total concentrations in air that were 2-5 orders of magnitude higher compared to other targeted chemical classes. A moderately strong and significant correlation (r = 0.625, p < 0.001) was observed for Gross Domestic Product index of the cities with total OPEs levels. Although large differences in FR levels were observed between some cities, when averaged across the five United Nations regions, the FR classes were more evenly distributed and varied by less than a factor of five. Results for Toronto, which is a 'reference city' for this study, agreed well with a more in-depth investigation of the level of FRs over different seasons and across eight sites representing different urban source sectors (e.g. traffic, industrial, residential and background). Future sampling periods under this project will investigate trace metals and other contaminant classes, linkages to toxicology, non-targeted analysis, and eventually temporal trends. The study provides a unique urban platform for evaluating global exposome.
Subject(s)
Air Pollutants , Environmental Pollutants , Flame Retardants , Air Pollutants/analysis , Cities , Environmental Monitoring , Environmental Pollutants/analysis , Flame Retardants/analysis , Halogenated Diphenyl Ethers/analysis , Humans , London , New York , Pilot ProjectsABSTRACT
Even though the outdoor air pollution and its major component Particulate Matter (PM) are recently classified as human carcinogen, attempts to elucidate the underlying mechanisms of PM toxicity are still crucial and continuing with in vitro approaches in various environmental circumstances. Present study investigated the genotoxicity (Comet assay) and the cytotoxicity (lactate dehydrogenase (LDH) leakage and the water-soluble tetrazolium (WST-1) assays) of 30 daily PM2.5 samples collected in the Kütahya province, to address their daily variability in effects with season (i.e. winter versus summer) and location (i.e. rural versus urban) using A549 human lung cancer epithelial cell line, as well as in relation to their chemical composition, specifically trace elements, organic carbon (OC) and elemental carbon (EC). The genotoxicity, measured by the percentage tail intensity (TI), of the daily PM2.5 samples at the traffic dense urban station was higher than that of the rural site for 80% of the parallel days. The genotoxicity was significant in the winter at the urban and in the summer at the rural site. Cytotoxicity was the highest for the winter urban samples. The PM2.5 mass, OC, and EC concentrations were not correlated to DNA damage, while there were correlations with Mn, Fe, Cu and Ba at the rural PM2.5 samples, and Mn, Co and Ni at the urban samples, respectively. The present study is confirming that the complex composition of PM2.5 originating from spatial and temporal changes can cause differences in the health effects.
Subject(s)
Air Pollutants/toxicity , Cytotoxins/toxicity , Particulate Matter/toxicity , A549 Cells , Air Pollution/adverse effects , Carbon/toxicity , Cell Line, Tumor , Comet Assay/methods , DNA Damage/drug effects , Environmental Monitoring/methods , Humans , Particle Size , SeasonsABSTRACT
In light of growing concern and insufficient knowledge on the negative impact of aircraft emissions on environmental health, this study strives to investigate the air burden of major and trace elements caused by general aviation, piston-engine, and turboprop aircraft, within the vicinity of Eskisehir Hasan Polatkan Airport (Eskisehir, Turkey). The levels of 57 elements were investigated, based on moss bag biomonitoring using Sphagnum sp., along with chemical analyses of lubrication oil and aviation gasoline fuel used in the aircraft's operations. Five sampling sites were selected within the vicinity of the airport area to capture spatial changes in the concentration of airborne elements. The study demonstrates that moss bag biomonitoring is a useful tool in the identification of differences in the air burden by major and trace elements that have concentrated downwind of the aircraft emission sources. Moreover, pollutant enrichment in the Sphagnum moss bags and elemental characterization of oil/fuel are in agreement suggesting that Pb, followed by Cd, Cu, Mo, Cr, Ni, Fe, Si, Zn, Na, P, Ca, Mg, and Al are dominant elements that shaped the general aviation aircraft emissions.
Subject(s)
Air Pollutants/analysis , Aircraft , Environmental Monitoring/methods , Sphagnopsida/chemistry , Airports , Chelating Agents/analysis , Gasoline , TurkeyABSTRACT
A field study was performed in a rural tunnel to determine pollutant concentrations, sources and on road vehicle emission factors (EFs) of particulate matter, trace metals, elemental carbon (EC), organic carbon (OC), benzene, toluene, ethyl benzene and xylenes (BTEX), and polycyclic aromatic hydrocarbons (PAHs). Emission factors (EFs) for polychlorinated naphthalenes (PCNs) and polychlorinated biphenyls (PCBs) were also determined. A 12-day extensive sampling campaign during morning and afternoon periods at inlet and exit stations of the tunnel was conducted. Morphology of the particles was also investigated by Scanning Electron Microcopy (SEM). Correlation analysis, factor analysis and diagnostic PAH ratios were utilized to identify emission sources of trace metals. Identified sources include brake wear (33%), resuspension of road dust (15%), tyre wear (12%), exhaust emissions (10%), and lubricants (9%). Based on the PAH diagnostic ratios, major sources of PAHs were estimated as diesel emissions. EFs were comparable with the literature and varied from 31.5 to 295.4â¯mgâ¯vehicle-1â¯km-1 with an average of 129.2⯱â¯80â¯mgâ¯vehicle-1â¯km-1 for PM2.5. PM2.5-10 EFs varied between 15.9 and 236.1â¯mgâ¯vehicle-1â¯km-1 with an average of 96⯱â¯30â¯mgâ¯vehicle-1â¯km-1. Average EC EFs were 40.3⯱â¯9.8â¯mgâ¯vehicle-1â¯km-1 for PM2.5 samples and 19.5⯱â¯0.5â¯mgâ¯vehicle-1â¯km-1 for PM2.5-10 samples while OC EFs were 33.7⯱â¯18 and 15.5⯱â¯8.4â¯mgâ¯vehicle-1â¯km-1 for fine and coarse particles, respectively. EFs of elements were generally 2 (Al) to 59 (Mg) times higher than those previously reported in the literature. Compared to literature, relatively higher EFs for Σ13PAHs (range: 48.1-168⯵gâ¯vehicle-1â¯km-1, average: 84.3⯱â¯46.4⯵gâ¯vehicle-1â¯km-1) were obtained. BTEX emission factors were in the range of 4.2⯱â¯4.7â¯mgâ¯vehicle-1â¯km-1 (mâ¯+â¯p-xylene) and 16.7⯱â¯10.5â¯mgâ¯vehicle-1â¯km-1 (toluene). Average EFs for ΣPCBs and ΣPCNs were 12.06⯱â¯5.3⯵gâ¯vehicle-1â¯km-1 and 88.9⯱â¯70.4â¯ngâ¯vehicle-1â¯km-1, respectively.
ABSTRACT
Atmospheric and concurrent soil samples were collected during winter and summer of 2014 at 41 sites in Kutahya, Turkey to investigate spatial and seasonal variations, sources, air-soil exchange, and associated carcinogenic risks of polycyclic aromatic hydrocarbons (PAHs) and polychlorinated biphenyls (PCBs). The highest atmospheric and soil concentrations were observed near power plants and residential areas, and the wintertime concentrations were generally higher than ones measured in summer. Spatial distribution of measured ambient concentrations and results of the factor analysis showed that the major contributing PAH sources in Kutahya region were the coal combustion for power generation and residential heating (48.9%), and diesel and gasoline exhaust emissions (47.3%) while the major PCB sources were the coal (thermal power plants and residential heating) and wood combustion (residential heating) (45.4%), and evaporative emissions from previously used technical PCB mixtures (34.7%). Results of fugacity fraction calculations indicated that the soil and atmosphere were not in equilibrium for most of the PAHs (88.0% in winter, 87.4% in summer) and PCBs (76.8% in winter, 83.8% in summer). For PAHs, deposition to the soil was the dominant mechanism in winter while in summer volatilization was equally important. For PCBs, volatilization dominated in summer while deposition was higher in winter. Cancer risks associated with inhalation and accidental soil ingestion of soil were also estimated. Generally, the estimated carcinogenic risks were below the acceptable risk level of 10-6. The percentage of the population exceeding the acceptable risk level ranged from <1% to 16%, except, 32% of the inhalation risk levels due to PAH exposure in winter at urban/industrial sites were >10-6.
Subject(s)
Air Pollutants/adverse effects , Polychlorinated Biphenyls/adverse effects , Polycyclic Aromatic Hydrocarbons/adverse effects , Power Plants , Seasons , Soil Pollutants/adverse effects , Environmental Monitoring , Humans , Neoplasms/epidemiology , Risk Assessment , TurkeyABSTRACT
Dry deposition of atmospheric 18 polycyclic aromatic hydrocarbon (PAH) components was investigated in the scope of the study by using surrogate snow samplers at 49 different sampling points in and around the city center of Erzurum, Turkey. Snow was sampled twice, the first of which was taken immediately after the first fresh snow cover and placed into aluminum trays to obtain dry deposition surface while the second sample was taken from the snow cover (accumulated snow) exposed to an 8-day dry deposition period and then analyzed and extracted. All the samples taken from the samplers were extracted using solid and liquid phase extraction and analyzed through GC-MS. It was observed that at the end of an 8-day dry period, snow samples enriched 5.5 times more in PAH components than the baseline. PAH deposition was determined to be influenced mainly by coal, mixed source, traffic, diesel fuel, and petrol fuel at 43, 27, 20, 8, and 2 % of sampling points, respectively. Local polluting sources were found to be effective on the spatial distribution of dry deposition of PAH components in urban area.