MXene-Decorated Nylon Mesh Filters for Improvement of Indoor Air Quality by PM2.5 Filtration.

Air pollution is a problem that is increasing day by day and poses a threat on a global scale. Particulate matter (PM) is one of the air pollutants that is the biggest concern regarding air quality. In order to control PM pollution, highly effective air filters are required. This is especially necessary for PM with a diameter of less than 2.5 micrometers (PM2.5), which poses a health risk to humans. In this study, we demonstrate for the first time the use of a two-dimensional titanium carbide (Ti3C2) MXene nanosheets-decorated nylon mesh (MDNM) as a low cost and highly efficient PM2.5 filter. This study develops a proof-of-concept method to capture PM2.5. Thanks to their high specific surface area and active surface-terminating groups, conductive MXene nanosheets have made nylon mesh filters promising candidates for air filtration. The developed filters used electrostatic force to capture PM2.5 and showed high removal efficiency (90.05%) when an ionizer was used and under an applied voltage of 10 V, while a commercial high-efficiency particulate air (HEPA) filter had a removal efficiency of 91.03% measured under identical conditions. The proposed filters, which stand out with their low energy consumption, low pressure drop (∼14 Pa), and cost-effectiveness, have the potential to be a strong competitor to conventional PM filter systems used in many fields.

Modification of Saharan dust size distribution during its transport over the Anatolian Plateau.

Particle number size distribution in dust plumes and its modification as the plume travels over the Anatolia were investigated by measuring particle number size distributions at two stations: one located on the Mediterranean coast of Turkey and the other on the Anatolian plateau. Clustering of backtrajectories revealed six trajectory clusters at the Marmaris station and nine clusters at the Ankara station. Cluster 6 in Marmaris and clusters 6, 7 and 9 in Ankara stations had the potential to transport Saharan dust to stations. Concentration of particles with D ≤ 1 µm increased during dust events in the Ankara station, but decreased at the Marmaris station. Higher PM1 concentrations during the non-dust period at the Marmaris station were attributed to the dominance of secondary particle formation on PM1 concentrations. Occurrence of sea salt episodes at the Marmaris station and anthropogenic episodes at the Ankara station affects the distribution of episodes. If different types of episodes are not differentiated and all episodes are considered as dust, it can lead to misleadingly high dust episodes in winter. Six Saharan dust episodes were sequentially intercepted first at the Marmaris and then at the Ankara stations. These episodes were used to study how dust size distribution is modified as the plume travels from the Mediterranean coast to central Anatolia. On the average, travel time between the two stations is 1-2 days. Particle number concentrations in 1 µm ≤ D ≤ 110 µm size range were consistently high at the Ankara station, indicating that local sources play a role in modifying the number size distribution as the plume travels over the Anatolian plateau.

Characterization and source apportionment of carbonaceous aerosols in fine particles at urban and suburban atmospheres of Ankara, Turkey.

In order to find the spatial distribution characteristics of elemental (EC) and organic (OC) carbon in fine particles, daily PM2.5 aerosol samples were collected at two different stations, between July 2014 and September 2015 in Ankara, Turkey. Concentrations of OC ranged from 2.1 to 42 µg m-3 at urban station. These concentrations were higher than those obtained for suburban station whose values ranged from 1.3 to 15 µg m-3. Concentrations of EC ranged from 0.7 to 4.9 µg m-3 at the urban station. As in OC case, the corresponding levels were higher than those measured for suburban station. The associated EC levels ranged from 0.1 to 3.4 µg m-3 for the suburban station. Daily changes in the levels of EC were larger than the OC levels. OC/EC ratios were lower with lower monthly variability in summer and higher with lower monthly variability in winter at the urban site. Medium and weak correlations were obtained between EC and OC in the winter and summer seasons, respectively, at both stations. Secondary organic carbon (SOC) was an important component of OC in PM2.5 at the urban and suburban sites. The winter SOC level was higher than the summer SOC level at the urban site but slightly lower than the summer SOC level at the suburban site. Total carbon was apportioned using factor analysis for the eight carbon fraction data (OC1, OC2, OC3, OC4, EC1, EC2, EC3, and OP). The main sources of pollutants in the urban and suburban settings were from vehicular emissions, biomass and coal combustions, and road dust.

Determination of the personal, indoor and outdoor exposure levels of inorganic gaseous pollutants in different microenvironments in an industrial city.

We measured SO2, NO2 and O3 concentrations during the summer and winter in Kocaeli, Turkey. The sampling was carried out indoors and outdoors at homes, schools and offices. Personal samplers were also used to determine personal exposures to these pollutants. High NO2 and SO2 concentrations were observed in outdoor samples collected close to locations characterized by heavy urban traffic. Concentrations of O3, on the other hand, were higher in rural areas around the city due to ozone distillation. For both sampling periods, the concentrations of outdoor SO2 and O3 were higher than for indoor and personal samples; however, the NO2 concentrations were higher in indoor and personal samples, indicating that outdoor sources significantly contribute to indoor SO2 and O3 levels and that indoor NO2 concentrations are primarily modulated by sources within buildings. Seasonal variations in pollutant concentrations showed statistically significant differences. Indoor and outdoor concentrations of NO2 and SO2 measured in the winter were higher than the levels measured in the summer; O3 concentrations, on the other hand, exhibited the opposite trend. Active-to-passive concentration ratios for NO2, SO2 and O3 were 0.99, 1.08 and 1.16, respectively; the corresponding outdoor ratios were 0.95, 0.99 and 1.00.

Chemical composition of Eastern Black Sea aerosol--preliminary results.

Trace element composition of atmospheric particles collected at a high altitude site on the Eastern Black Sea coast of Turkey was investigated to understand atmospheric transport of pollutants to this semi-closed basin. Aerosol samples were collected at a timber-storage area, which is operated by the General Directorate of Forestry. The site is situated at a rural area and is approximately 50 km to the Black Sea coast and 200 km to the Georgia border of Turkey. Coarse (PM2.5-10) and fine (PM2.5) aerosol samples were collected between 2011 and 2013 using a "stacked filter unit". Collected samples were shipped to the Middle East Technical University in Ankara, where Na, Mg, Al, Si, S, K, Ca, Ti, V, Cr, Mn, Fe, Ni, Cu, Zn, As, Ba, Pb were measured by Energy dispersive x-ray fluorescence technique (EDXRF). Comparison of measured concentrations of elements with corresponding data generated at other parts of Turkey demonstrated that concentrations of pollution derived elements are higher at Eastern Black Sea than their corresponding concentrations measured at other parts of Turkey, which is attributed to frequent transport of pollutants from north wind sector. Positive matric factorization revealed four factors including three anthropogenic and a crustal factor. Southeastern parts of Turkey, Georgia and Black Sea coast of Ukraine were identified as source regions affecting composition of particles at our site, using trajectory statistics, namely "potential source contribution function" (PSCF).

C5-C12 volatile organic compounds at roadside, residential, and background locations in Ankara, Turkey: temporal and spatial variations and sources.

Concentrations of 91 volatile organic compounds (VOCs) ranging from C5 to C12 were measured at three sites in Ankara, the capital of Turkey, in the summer of 2003 and winter of 2004. Samples were collected at roadside, residential and background stations at consecutive 4-hr intervals over a 24-hr period for six weeks in each season. Air samples were collected onto cartridges packed with Tenax TA and Carbopack B resins and analyzed by thermal desorption, followed by gas chromatography coupled to a mass selective detector (GC/MSD). Time resolved data provided information on ambient levels, temporal and spatial variations and sources of VOCs in Ankara. Toluene is the most abundant compound at all sites with and average concentration of 13.1 ?g m(-3). The mean concentrations of benzene are 12.6, 5.2, and 2.4 ?g m(-3) during winter at roadside, residential and background stations, respectively. Diurnal variation in the data together with toluene to benzene concentration ratio (T:B) that is close to 2.0 indicated the influence of traffic related emissions at residential and roadside stations during winter season. Higher T:B ratio observed at residential and background stations during summer period and correlation analysis indicated additional VOC sources. Temporal variations and low m,p-xylene to ethylbenzene ratio (mpX:E) indicated that transported air mass is the major VOC source influencing VOC concentrations measured at the background station.

Improvement of uptake rate equations depending on meteorological conditions for 25 volatile organic compounds.

Stainless steel passive (diffusive) sampling tubes manufactured by Gradko International Ltd. (UK) were filled with Chromosorb 106 (Supelco) and evaluated to determine the uptake rates of 31 VOCs over six months under different meteorological conditions in a suburban area of Ankara, Turkey. The URs have been calculated, and dependence on such meteorological parameters as temperature, relative humidity and wind speed has been established for the 31 VOCs. The URs of the 31 VOCs measured in this study showed a statistically significant decreasing trend with rising temperature; and weaker, but again statistically significant, increasing trends with increasing relative humidity and wind speed. This study has demonstrated that the URs of VOCs are affected by meteorological parameters, and this dependence should be taken into account when attempting to generate reliable data through passive sampling. A multiple linear regression equation in which temperature, relative humidity and wind speed were used as independent variables was generated for 25 of the 31 tested VOCs.

An approach to measure trace elements in particles collected on fiber filters using EDXRF.

A method developed for analyzes of large number of aerosol samples using Energy Dispersive X-Ray Fluorescence (EDXRF) and its performance were discussed in this manuscript. Atmospheric aerosol samples evaluated in this study were collected on cellulose fiber (Whatman-41) filters, employing a Hi-Vol sampler, at a monitoring station located on the Mediterranean coast of Turkey, between 1993 and 2001. Approximately 1700 samples were collected in this period. Six-hundred of these samples were analyzed by instrumental neutron activation (INAA), and the rest were archived. EDXRF was selected as an analytical technique to analyze 1700 aerosol samples because of its speed and non-destructive nature. However, analysis of aerosol samples collected on fiber filters with a surface technique such as EDXRF was a challenge. Penetration depth calculation performed in this study revealed that EDXRF can obtain information from top 150µm of our fiber filter material. Calibration of the instrument with currently available thin film standards caused unsatisfactory results since the actual penetration depth of particles into fiber filters were much deeper than 150µm. A method was developed in this manuscript to analyze fiber filter samples quickly with XRF. Two hundred samples that were analyzed by INAA were divided into two equal batches. One of these batches was used to calibrate the XRF and the second batch was used for verification. The results showed that developed method can be reliably used for routine analysis of fiber samples loaded with ambient aerosol.

Air pollution forecasting in Ankara, Turkey using air pollution index and its relation to assimilative capacity of the atmosphere.

Spatial and temporal variations in concentrations of CO, NO, NO(2), SO(2), and PM(10), measured between 1999 and 2000, at traffic-impacted and residential stations in Ankara were investigated. Air quality in residential areas was found to be influenced by traffic activities in the city. Pollutant ratios were proven to be reliable tracers to differentiate between different sources. Air pollution index (API) of the whole city was calculated to evaluate the level of air quality in Ankara. Multiple linear regression model was developed for forecasting API in Ankara. The correlation coefficients were found to be 0.79 and 0.63 for different time periods. The assimilative capacity of Ankara atmosphere was calculated in terms of ventilation coefficient (VC). The relation between API and VC was investigated and found that the air quality in Ankara was determined by meteorology rather than emissions.

Effect of meteorological parameters on fine and coarse particulate matter mass concentration in a coal-mining area in Zonguldak, Turkey.

In this work, the effect of meteorological parameters and local topography on mass concentrations of fine (PM2.5) and coarse (PM2.5-10) particles and their seasonal behavior was investigated. A total of 236 pairs of samplers were collected using an Anderson Dichotomous sampler between December 2004 and October 2005. The average mass concentrations of PM2.5, PM2.5-10, and particulate matter less than 10 microm in aerodynamic diameter (PM10) were found to be 29.38, 23.85, and 53.23 microg/m3, respectively. The concentrations of PM2.5 and PM10 were found to be higher in heating seasons (December to May) than in summer. The increase of relative humidity, cloudiness, and lower temperature was found to be highly related to the increase of particulate matter (PM) episodic events. During non-rainy days, the episodic events for PM2.5 and PM10 were increased by 30 and 10.7%, respectively. This is a result of the extensive use of fuel during winter for heating purposes and also because of stagnant air masses formed because of low temperature and low wind speed over the study area.

Particulate matter (PM(2.5), PM(10-2.5), and PM(10)) and children's hospital admissions for asthma and respiratory diseases: a bidirectional case-crossover study.

Epidemiological studies reported adverse effects of air pollution on the prevalence of respiratory diseases in children. The purpose of this study was to examine the association between air pollution and admissions for asthma and other respiratory diseases among children who were younger than 15 yr of age. The study used data on respiratory hospital admissions and air pollutant concentrations, including thoracic particulate matter (PM(10)), fine (PM(2.5)), and coarse (PM(10-2.5)) particulate matter in Zonguldak, Turkey. A bidirectional case-crossover design was used to calculate odds ratios for the admissions adjusted for daily meteorological parameters. Significant increases were observed for hospital admissions in children for asthma, allergic rhinitis (AR), and upper (UPRD) and lower (LWRD) respiratory diseases. All fraction of PM in children showed significant positive associations with asthma admissions. The highest association noted was 18% rise in asthma admissions correlated with a 10-microg/m(3) increase in PM(10-2.5) on the same day of admissions. The adjusted odds ratios for exposure to PM(2.5) with an increment of 10 microg/m(3) were 1.15 and 1.21 for asthma and allergic rhinitis with asthma, respectively. PM(10) exerted significant effects on hospital admissions for all outcomes, including asthma, AR, UPRD, and LWRD. Our study suggested a greater effect of fine and coarse PM on asthma hospital admissions compared with PM(10) in children.

Multivariate statistics to investigate metal contamination in surface soil.

The modification of soil composition in the urbanized area of Ankara due to wet-dry deposition and pollution-derived particles from the atmosphere is investigated by analyzing 120 surface soil samples, collected from the urbanized area and its un-urbanized surrounding, for major, minor and trace elements. Concentrations of elements from human activity (e.g. Cd, Pb, Cr, Zn, Cu and Ca) in the urbanized area were higher than their corresponding concentrations in global average soil and soil in un-urbanized areas outside the urbanized area. Metal contents in soil were very high in densely populated districts and around some industrial facilities. The only exception was Pb distribution, which was more dispersed, due to the nature of motor vehicle emissions. Alteration of the Cd, Zn, Cu and Cr content of soil was confined to the inhabited and industrial areas, whereas enrichment factors of these elements were close to unity in the remaining study area. Factor analysis identified two polluted soil factor associations. One factor includes elements, such as Zn and Cd, which had high factor scores in inhabited areas and the other factor (high loading of Pb) represents soil polluted by motor vehicle emissions.

Determination of volatile organic compounds in different microenvironments by multibed adsorption and short-path thermal desorption followed by gas chromatographic-mass spectrometric analysis.

A multiphase assurance approach was developed for the accurate and precise determination of volatile organic compounds (VOCs) in different microenvironments. This approach includes (i) development of a method including adsorption of VOCs onto a multisorbent media followed by short-path thermal desorption (SPTD) pre-concentration and gas chromatography (GC) coupled to a mass spectrometry (MS) quantification, (ii) validation of the sampling and analytical method and (iii) validation of the data using a multidimensional procedure. Tenax TA and Carbopack B sorbent combinations were used to collect 102 individual VOCs ranging from C5 to C12. Method parameters including thermal desorption temperature, desorption time and cryofocusing temperature were optimized. The average recoveries and method detection limits (MDL) for the target analytes were in the range 80-100% and 0.01-0.14 ppbv, respectively. The method also showed good linearity (R2 > 0.99) and precision (<8%) values. Validation of the method was performed under real environmental conditions at a gas station, in an office and a residential household to examine the influence of variation in meteorological conditions such as temperature and relative humidity and a wide range of VOC concentrations. The sampling and analytical method resulted in successful determination of VOC in different microenvironments. Finally, validation of the data was performed by assessing fingerprint and time series plots and correlation matrices together with meteorological parameters such as mixing height, wind speed and temperature. The data validation procedure provided detection of both faulty data and air pollution episodes.

Investigation of soil multi-element composition in Antalya, Turkey.

The chemical composition of 73 surface soil samples collected at the city of Antalya were analyzed for major, minor and trace elements to assess distribution of soil pollution, due to deposition of pollution-derived particles from the atmosphere. Comparison with data from rural area and distribution maps demonstrated that the composition of soil by metals is not significantly modified by anthropogenic activities in most of the city and its surroundings. In these areas, observed concentrations can be largely accounted for by occurrence of elements in aluminasilicate matrix of soil. However, soil composition is altered substantially close to major industries and at the settlement districts. In such limited areas, concentrations of anthropogenic elements such as Cd, Pb, Zn, Cu and Cr are factors of 20-50 higher than their concentrations in unperturbed soil. Factor analysis revealed three groups of elements that differ in their distributions. One of these components is unperturbed soil component, which is distributed uniformly in the study area; the second one is polluted soil, which is mostly confined to settlement areas and around industries; and the third is a mixed marine and motor vehicle impacted soil component, which occurred at the coastal parts of the city.