In this research, gasoline vapours including Benzene, Toluene, Xylene (BTX) and Total Volatile Organic Compounds (TVOCs) emitted from vent pipes of underground storage tanks (USTs) were measured at six gas stations in Tehran. Thereafter, gas station No. 29 was selected as a pilot station and equipped with a vapour control system. The vapours were measured during the summer of 2013 and winter of 2014 in two states, before and at the time of gasoline discharge from a petrol tanker to the UST. The results reveal that the average of BTX and TVOCs are 161.22, 200.81, 229 and 647.01 ppm, respectively, higher than the World Health Organisation (WHO) guidelines. The average of TVOCs and BTX in the situation in which the control system is inactive at the pilot station, are 259.13, 55.9, 73.03 and 96.88 ppm, respectively. After activating the control system at the pilot station, the VOCs were reduced by 0.01 ppm. Almost 99.99% control was obtained for this system and 87% of the people living around the pilot station were satisfied and no longer had any complaints about the bad odour of VOCs. It can be concluded that gasoline discharge from the petrol tanker to UST, is the main reason behind the overproduction of VOCs in Tehran's gas stations (P<0.001). So, the most important element is to reduce VOCs at Tehran's gas stations by installing a vapour control systems in all the stations and activating the systems at the time of gasoline discharge.

This study was conducted to identify and quantify the sources of selected volatile organic compounds (VOCs) and fine particulate matter (PM2.5) by using a partially constrained source apportionment model suitable for multiple time resolution data. Hourly VOC, 12-h and 24-h PM2.5 speciation data were collected during three seasons in 2013. Eight factors were retrieved from the Positive Matrix Factorization solutions and adding source profile constraints enhanced the interpretability of source profiles. Results showed that the evaporative emission factor was the largest contributor (25%) to VOC mass concentration, while the largest contributor to PM2.5 mass concentration was soil dust/regional transport related factor (26%). In terms of risk prioritization, traffic/industry related factor was the major cause for benzene, ethylbenzene, Cr, and polycyclic aromatic hydrocarbons (29–69%) while petrochemical related factor contributed most to the Ni risk (36%). This indicated that a larger contributor to mass concentration may not correspond to a higher risk.

Environmental health studies commonly quantify subjects' pollution exposure in their neighborhood. How this neighborhood is defined can vary, however, leading to different approaches to quantification whose impacts on exposure levels remain unclear. We explore the relationship between neighborhood definition and exposure assessment. NO2, benzene, PM10 and PM2.5 exposure estimates were computed in the vicinity of 10,825 buildings using twelve exposure assessment techniques reflecting different definitions of “neighborhood”. At the city scale, its definition does not significantly influence exposure estimates. It does impact levels at the building scale, however: at least a quarter of the buildings' exposure estimates for a 400 m buffer differ from the estimated 50 m buffer value (±1.0 μg/m3 for NO2, PM10 and PM2.5; and ±0.05 μg/m3 for benzene). This variation is significantly related to the definition of neighborhood. It is vitally important for investigators to understand the impact of chosen assessment techniques on exposure estimates.

In this study, reusable poly(alkoxysilane) organogels with high absorption capacities were synthesized by the condensation of a cyclo aliphatic glycol (UNOXOL™) and altering the chain length of the alkyltriethoxysilanes. The structural and thermal properties of cross-linked poly(alkoxysilane) polymers were determined by FTIR, solid-state 13C and 29Si CPMAS NMR and TGA. The oil absorbency of poly(alkoxysilane)s was determined through oil absorption tests, absorption and desorption kinetics. Results showed that the highest oil absorbency capacities were found to be 295% for hexane, 389% for euro diesel, 428% for crude oil, 652% for gasoline, 792% for benzene, 792% for toluene, 868% for tetrahydrofuran, and 1060% for dichloromethane for the poly(alkoxysilane) gels based on UNOXOL™ and dodecyltriethoxysilane. Owing to their hydrophobic structure, the poly(alkoxysilane) organogels can selectively absorb crude oil from water. The reusability of the absorbents was quantitatively investigated, demonstrating that absorbents can be used effectively at least nine times.

Measurements for indoor air quality assessment were carried out in Painting and Printmaking Department of Anadolu University Faculty of Fine Arts in Turkey. Concentrations of nitrogen dioxide (NO2), ozone (O3) and 29 Volatile Organic Compounds (VOCs) were measured simultaneously by using diffusive samplers. Simultaneous outdoor measurements were also performed at some sampling points. Analyses of NO2 and ozone samples were performed by using ion chromatography and VOCs were analyzed by using gas chromatography-mass spectrometry. Indoor NO2 and ozone concentrations varied between 13.47–89.77 μg m−3 and 3.89–51.82 μg m−3, respectively. Average indoor NO2 concentration was obtained as 35.37 ± 10.9 μg m−3. Indoor/outdoor NO2 ratio (I/O) was found as 1.44 ± 0.4 which indicated the presence of some indoor sources. Average indoor ozone concentration was 9.97 ± 4.4 μg m−3 and I/O ratio was obtained lower than 1 (0.46 ± 0.4). The highest VOC concentrations were observed at workshops where oil painting and stained glass studies were performed. Especially, the concentrations obtained from the stained glass workshop (benzene: 3.98 ± 1.3 μg m−3, toluene: 999.33 ± 104.2 μg m−3, ethly benzene: 66.06 ± 16.1 μg m−3, m,p xylene: 129.44 ± 33.1 μg m−3, o-xylene: 76.14 ± 23.1 μg m−3) were much higher than the other sampling points. Toluene concentrations exceeded the WHO (World Health Organization) limit value (260 μg m−3 weekly average) at 40% of the sampling points. Cancer risks were estimated by using the personal exposure concentrations. Lifetime cancer risks for the people working in the department such as faculty members and technicians were obtained higher than USEPA acceptable risk value (1 × 10−6) while the risks for the students were below this value.

Two Source oils and five field collected oil residues from the Deepwater Horizon incident were chemically characterized. Water accommodated fractions (WAFs) of the Source oils and two of the field-weathered oils were prepared to evaluate the impact of natural weathering on the chemical composition and the acute toxicity of the WAFs. Toxicity test species representing different tropic levels were used (the primary producer Skeletonema costatum (algae) and the herbivorous copepod Acartia tonsa). The results suggest that the potential for acute toxicity is higher in WAFs from non-weathered oils than WAFs from the field weathered oils. The Source oils contained a large fraction of soluble and bioavailable components (such as BTEX (benzene, toluene, ethyl benzene, xylenes) and naphthalene), whereas in the surface collected oils these components were depleted by dissolution into the water column as the oil rose to the surface and by evaporative loss after reaching the sea surface.

To develop an efficient adsorbent for humic acid, the present study represents the first attempt to investigate the capability of zeolitic imidazole frameworks to remove humic acid from water. Zeolitic imidazole framework-8 (ZIF-8) is particularly selected as a prototype ZIF to adsorb humic acid owing to its high stability in aqueous solutions. ZIF-8 was synthesized and characterized using scanning electronic microscopy (SEM), powder X-ray diffraction pattern (PXRD), Fourier transform infrared spectroscopy (FT-IR), and thermogravimetric analyzer (TGA) and then used to adsorb humic acid under various conditions. The structure of ZIF-8 was found to remain intact after the exposure to humic acid in water. Factors affecting the adsorption were examined, including solid-to-liquid ratio, mixing time, temperature, pH, presence of salt, and surfactants. The adsorption capacity of ZIF-8 was found to be much higher than that of activated carbon, fly ash, zeolites, graphite, etc., showing its promising potential for removal of humic acid. The adsorption mechanism could be attributed to the electrostatic interaction between the positive surface of ZIF-8 and the acidic sites of humic acid, as well as the π–π stacking interaction between imidazole of ZIF-8 and benzene rings of humic acid. The humic acid adsorption to ZIF-8 could be enhanced in the acidic conditions, and the adsorption process remained highly stable in the solutions of a wide range of NaCl concentrations. ZIF-8 can be also regenerated by simple ethanol-washing process and reused for humic acid adsorption. These features enable ZIF-8 to be an efficient and stable adsorbent to remove humic acid from water.

Exposure to benzene has been associated with multiple severe impacts on health. This notwithstanding, at most monitoring stations, benzene is not monitored on a regular basis. Data were used from two different monitoring stations located on the eastern Mediterranean coast: (1) a traffic monitoring station in Tel Aviv located in an urban region with heavy traffic and (2) a general air quality monitoring station in Haifa Bay located in Israel’s main industrial region. At each station, hourly, daily, monthly, seasonal, and annual data of benzene, NO ₓ , mean temperature, relative humidity, inversion level, and temperature gradient were analyzed over 3 years: 2008, 2009, and 2010. A prediction model for benzene rates based on NO ₓ levels (which are monitored regularly) was developed to contribute to a better estimation of benzene. The severity of benzene pollution was found to be considerably higher at the traffic monitoring station than at the general air quality station, despite the location of the latter in an industrial area. Hourly, daily, monthly, seasonal, and annual patterns have been shown to coincide with anthropogenic activities (traffic), the day of the week, and atmospheric conditions. A strong correlation between NO ₓ and benzene allowed the development of a prediction model for benzene rates based on NO ₓ , the day of the week, and the month. The model succeeded in predicting the benzene values throughout the year. The prediction model suggested in this study might be useful for identifying potential risk of benzene in other urban environments.

In indirect olfactometry analysis, to avoid condensation or adsorption processes during or storage of the sample, containers made of suitable materials should be used. Also, reaction between the chemicals during transport from the source of the odour to the research laboratory is an important process which can influence on examinations’ results. Study included determination of the odour and compound concentrations of six gas mixtures. Gas samples were collected by silicone hoses into Tedlar® bags and tested by Nasal Ranger, SM-100 olfactometers and Photovac Voyager gas chromatograph. Time of keeping gas in bags was 78 h, and concentration of compounds was measured every hour, eight times per day. For benzene, acetone, 1,1-dichloroethylene, c-1,2-dichloroethylene, t-1,2-dichloroethylene, methyl ethyl ketone and vinyl chloride, 100 % decrease of concentration has been noticed within 78 h of holding in the bag. Average rate of loss of most compounds concentration was from 0.01 to 2.50 % for the first 30 h and from 0.35 to 18.50 % during the last 48 h of examination. Decreasing of odour concentration measured by Nasal Ranger (NR) in all series was between 0.00 and 4.98 % till 30 h, between 1.91 and 100 % in the last 48 h of test and between 1.61 and 100 % in 78 h. In case of odour concentration measured by SM, those values were, respectively, 1.26–4.93 %, 1.39–4.93 % and 2.40–3.18 %. Values of average rate of intensity decreasing were, respectively, 0.77–1.75 %, 2.36–4.67 % and 1.18–2.07 %. Statistically significant correlation coefficients for compound concentrations and intensity, odour concentration obtained by SM-100 as well as NR were, respectively, 0.55–0.97, 0.47–0.99 and 0.37–0.98.

The simultaneous aerobic removal of a mixture of benzene, toluene, ethylbenzene, and o,m,p-xylene (BTEX); cis-dichloroethylene (cis-DCE); and trichloroethylene (TCE) from the artificially contaminated water using an indigenous bacterial isolate identified as Pseudomonas plecoglossicida immobilized on waste scrap tyres was investigated. Suspended and immobilized conditions were compared for the removal of these volatile organic compounds. For the immobilized system, toluene, benzene, and ethylbenzene were completely removed, while the highest removal efficiencies of 99.0 ± 0.1, 96.8 ± 0.3, 73.6 ± 2.5, and 61.6 ± 0.9 % were obtained for o-xylene, m,p-xylene, TCE, and cis-DCE, respectively. The sorption kinetics of contaminants towards tyre surface was also evaluated, and the sorption capacity generally followed the order of toluene > benzene > m,p-xylene > o-xylene > ethylbenzene > TCE > cis-DCE. Scrap tyres showed a good capability for the simultaneous sorption and bioremoval of BTEX/cis-DCE/TCE mixture, implying a promising waste material for the removal of contaminant mixture from industrial wastewater or contaminated groundwater.