Benzene, Toluene, Ethylbenzene, Xylenes Research Articles

Investigation of in-cabin volatile organic compounds (VOCs) in taxis; influence of vehicle's age, model, fuel, and refueling

The air pollutant species and concentrations in taxis' cabins can present significant health impacts on health. This study measured the concentrations of benzene, toluene, ethylbenzene, xylene (BTEX), formaldehyde, and acetaldehyde in the cabins of four different taxi models. The effects of taxi's age, fuel type, and refueling were investigated. Four taxi models in 3 age groups were fueled with 3 different fuels (gas, compressed natural gas (CNG), and liquefied petroleum gas (LPG)), and the concentrations of 6 air pollutants were measured in the taxi cabins before and after refueling. BTEX, formaldehyde, and acetaldehyde sampling were actively sampled using NIOSH methods 1501, 2541, and 2538, respectively. The average BTEX concentrations for all taxi models were below guideline values. The average concentrations (±SD) of formaldehyde in Model 1 to Model 4 taxis were 889 (±356), 806 (±323), 1144 (±240), and 934 (±167) ppbv, respectively. Acetaldehyde average concentrations (±SD) in Model 1 to Model 4 taxis were 410 (±223), 441 (±241), 443 (±210), and 482 (±91) ppbv, respectively. Refueling increased the in-vehicle concentrations of pollutants primarily the CNG and LPG fuels. BTEX concentrations in all taxi models were significantly higher for gasoline. Taxi age inversely affected formaldehyde and acetaldehyde. In conclusion, it seems that refueling process and substitution of gasoline with CNG and LPG can be considered as solutions to improve in-vehicle air concentrations for taxis.

Distinguishing Petroleum (Crude Oil and Fuel) From Smoke Exposure within Populations Based on the Relative Blood Levels of Benzene, Toluene, Ethylbenzene, and Xylenes (BTEX), Styrene and 2,5-Dimethylfuran by Pattern Recognition Using Artificial Neural Networks.

Studies of exposure to petroleum (crude oil/fuel) often involve monitoring benzene, toluene, ethylbenzene, xylenes (BTEX), and styrene (BTEXS) because of their toxicity and gas-phase prevalence, where exposure is typically by inhalation. However, BTEXS levels in the general U.S. population are primarily from exposure to tobacco smoke, where smokers have blood levels on average up to eight times higher than nonsmokers. This work describes a method using partition theory and artificial neural network (ANN) pattern recognition to classify exposure source based on relative BTEXS and 2,5-dimethylfuran blood levels. A method using surrogate signatures to train the ANN was validated by comparing blood levels among cigarette smokers from the National Health and Nutrition Examination Survey (NHANES) with BTEXS and 2,5-dimethylfuran signatures derived from the smoke of machine-smoked cigarettes. Classification agreement for an ANN model trained with relative VOC levels was up to 99.8% for nonsmokers and 100.0% for smokers. As such, because there is limited blood level data on individuals exposed to crude oil/fuel, only surrogate signatures derived from crude oil and fuel were used for training the ANN. For the 2007-2008 NHANES data, the ANN model assigned 7 out of 1998 specimens (0.35%) and for the 2013-2014 NHANES data 12 out of 2906 specimens (0.41%) to the crude oil/fuel signature category.

Produced Water Surface Spills and the Risk for BTEX and Naphthalene Groundwater Contamination

The widespread use of unconventional drilling involving hydraulic fracturing (“fracking”) has allowed for increased oil-and-gas extraction, produced water generation, and subsequent spills of produced water in Colorado and elsewhere. Produced water contains BTEX (benzene, toluene, ethylbenzene, xylene) and naphthalene, all of which are known to induce varying levels of toxicity upon exposure. When spilled, these contaminants can migrate through the soil and contaminant groundwater. This research modeled the solute transport of BTEX and naphthalene for a range of spill sizes on contrasting soils overlying groundwater at different depths. The results showed that benzene and toluene were expected to reach human health relevant concentration in groundwater because of their high concentrations in produced water, relatively low solid/liquid partition coefficient and low EPA drinking water limits for these contaminants. Peak groundwater concentrations were higher and were reached more rapidly in coarser textured soil. Risk categories of “low,” “medium,” and “high” were established by dividing the EPA drinking water limit for each contaminant into sequential thirds and modeled scenarios were classified into such categories. A quick reference guide was created that allows the user to input specific variables about an area of interest to evaluate that site’s risk of groundwater contamination in the event of a produced water spill. A large fraction of produced water spills occur at hydraulic-fracturing well pads; thus, the results of this research suggest that the surface area selected for a hydraulic-fracturing site should exclude or require extra precaution when considering areas with shallow aquifers and coarsely textured soils.

Neurodevelopmental and neurological effects of chemicals associated with unconventional oil and natural gas operations and their potential effects on infants and children

Heavy metals (arsenic and manganese), particulate matter (PM), benzene, toluene, ethylbenzene, xylenes (BTEX), polycyclic aromatic hydrocarbons (PAHs) and endocrine disrupting chemicals (EDCs) have been linked to significant neurodevelopmental health problems in infants, children and young adults. These substances are widely used in, or become byproducts of unconventional oil and natural gas (UOG) development and operations. Every stage of the UOG lifecycle, from well construction to extraction, operations, transportation and distribution can lead to air and water contamination. Residents near UOG operations can suffer from increased exposure to elevated concentrations of air and water pollutants. Here we focus on five air and water pollutants that have been associated with potentially permanent learning and neuropsychological deficits, neurodevelopmental disorders and neurological birth defects. Given the profound sensitivity of the developing brain and central nervous system, it is reasonable to conclude that young children who experience frequent exposure to these pollutants are at particularly high risk for chronic neurological diseases. More research is needed to understand the extent of these concerns in the context of UOG, but since UOG development has expanded rapidly in recent years, the need for public health prevention techniques, well-designed studies and stronger state and national regulatory standards is becoming increasingly apparent.

Study on the sediment characteristics of the snow in a typical residential community and its integrated biological treatment pattern in Harbin.

Winter cities have severe shortages of water resources. The effective classification and recycling of urban water resources that are available here are therefore significant for the sustainable utilization of water in winter cities, and snow is a potential water resource. In this research, the water quality of the snow and the pollutant composition in the vehicle roads of a typical residential community of Harbin are analyzed. It is concluded that there is a large amount of suspended substances, including chemical oxygen demand (COD), salt, ammonia, and oil in this snow. There are 27 main pollutants. The oily substances are dominated by hexadecane and are accompanied by toxic substances, including benzene, toluene, ethylbenzene, xylene (BTEX), and naphthalene. As snow is a carrier of pollutants, the underground space of the urban shallow green belt is proposed to be used to establish a snow-melting system that would integrate biological treatment devices. This method allows the year-round collection, storage, and utilization of rainwater for use in city planning and municipal technology, realizing multiple objectives and having a significant influence on further urban development.

Citrate Addition Increased Phosphorus Bioavailability and Enhanced Gasoline Bioremediation.

Phosphorus (P) bioavailability often limits gasoline biodegradation in calcareous cold-region soils. One possible method to increase P bioavailability in such soils is the addition of citrate. Citrate addition at the field scale may increase hydrocarbon degradation by: (i) enhancing inorganic and organic P dissolution and desorption, (ii) increasing hydrocarbon bioavailability, and/or (iii) stimulating microbial activity. Alternatively, citrate addition may inhibit activity due to competitive effects on carbon metabolism. Using a field-scale in situ biostimulation study, we evaluated if citrate could stimulate gasoline degradation and what the dominant mechanism of this stimulation will be. Two large bore injectors were constructed at a site contaminated with gasoline, and a biostimulation solution of 11 mM MgSO, 1 mM HPO, and 0.08 mM HNO at pH 6.5 in municipal potable water was injected at ∼5000 L d for about 4 mo. Following this, 10 mM citric acid was incorporated into the existing biostimulation solution and the site continued to be stimulated for 8 mo. After citrate addition, the bioavailable P fraction in groundwater and soil increased. Iron(II) groundwater concentrations increased and corresponded to decreases in benzene, toluene, ethylbenzene, xylenes (BTEX) in groundwater, as well as a decrease in F1 in the soil saturated zone. Overall, citrate addition increased P bioavailability and may stimulate anaerobic microbial activity, resulting in accelerated anaerobic gasoline bioremediation in cold-region calcareous soils.

Experimental study on combustion and emission performance of a spark-ignition engine fueled with water containing acetone-gasoline blends

Acetone is widely recognized as a major organic solvent and also a basic ingredient for varnishes and paints. In comparison with ethanol, acetone has more attractive properties as a potential alternative fuel such as its higher energy density, heating value, and volatility. However, the water content in acetone production would lead to a high cost for dehydration, and may prohibit acetone from being widely used in internal combustion engines. This has prompted research on using water containing acetone as a potential alternative fuel. In this study, various acetone-gasoline blends such as A10 (10vol% acetone and 90vol% gasoline by volume), A20 (20vol% acetone and 80vol% gasoline by volume), A19.5W0.5 (19.5vol% acetone and 0.5vol% water and 80vol% gasoline) and A19W1 (19vol% acetone and 1vol% water and 80vol% gasoline) were used as fuels in a port-fuel injection (PFI) spark ignition (SI) engine. The performance of test fuels was compared with that of G100 (gasoline) under various equivalence ratios (Φ) from 0.83 to 1.25 and at engine loads of 3 and 5bar BMEP. In addition, aromatic compound emissions such as benzene, toluene, ethylbenzene, xylene (BTEX) were also measured by gas chromatograph (GC) with mass spectrometer and flame ionization detector. The results showed that A19W1 generally had a more advanced combustion phasing, higher brake thermal efficiency, and lower carbon monoxide (CO), nitrogen oxide (NOx) and BTEX than those of other test fuels. Therefore, water containing acetone-gasoline blends could be used as a good alternative fuel due to the improvement of engine performance and reduction of emissions.

Avaliação ambiental de BTEX (benzeno, tolueno, etilbenzeno, xilenos) e biomarcadores de genotoxicidade em trabalhadores de postos de combustíveis

Resumo Introdução: trabalhadores de postos de combustíveis estão expostos às diversas substâncias químicas presentes no ambiente de trabalho, destacando-se entre elas o benzeno, devido às suas propriedades carcinogênicas. Objetivo: avaliar os danos genotóxicos relacionados à exposição ocupacional ao BTEX (benzeno, tolueno, etilbenzeno, xilenos) em trabalhadores de cinco postos de combustíveis do município do Rio de Janeiro, RJ. Metodologia: foram analisadas concentrações de BTEX no ar; atividades das enzimas catalase e glutationa S-transferase; e ensaio cometa em amostras de sangue total de 97 trabalhadores. Resultados: as concentrações de BTEX estavam dentro dos valores preconizados pela NR 15, incluindo Anexo 13-A. Entretanto, uma oscilação nos resultados de ensaio cometa foi observada entre os trabalhadores dos diferentes postos de combustíveis, principalmente em trabalhadores de postos com menores concentrações de benzeno. Discussão: esse resultado está de acordo com a literatura científica atual, que indica uma curva dose-resposta supralinear para o benzeno, observando-se em baixas concentrações um aumento não linear do risco de leucemia, provavelmente relacionado à maior metabolização do benzeno e à maior produção de seus metabólitos tóxicos nessas concentrações. Conclusão: os resultados deste estudo sugerem que a exposição ao BTEX, mesmo em baixas concentrações, contribui para o risco genotóxico à saúde humana.

Oil plume simulations: Tracking oil droplet size distribution and fluorescence within high-pressure release jets

ABSTRACT Optical measurements have been used during oil spill response for more than three decades to determine oil presence in slicks and plumes. Oil surveillance approaches range from simple (human eyeball) to the sophisticated (sensors on AUVs, aircraft, satellites). In situ fluorometers and particle size analyzers were deployed during the Deepwater Horizon (DWH) Gulf of Mexico oil spill to track shallow and deep subsea plumes. Uncertainties regarding instrument specifications and capabilities during DWH necessitated performance testing of sensors exposed to simulated, dispersed oil plumes. Seventy-two wave tank experiments were conducted at the Bedford Institute of Oceanography. Simulated were oil releases with varying parameters such as oil release rate, oil temperature (reservoir temp ~ 80 °C), water temperature (<8 °C and >15 °C), oil type, dispersant type (Corexit 9500 and Finasol OSR52) and dispersant to oil ratio (DOR). Plumes of Alaskan North Slope Crude (ANS), South Louisiana Crude (SLC) and IFO-120 oils were tracked using in situ fluorescence, droplet size distribution (DSD), total petroleum hydrocarbons (TPH) and benzene-toluene-ethylbenzene-xylene (BTEX). For the lighter SLC, bimodal droplet size with mean diameter < 70 μm was achieved for 1:20 and 1:100 DOR, regardless of water temperature. Similarly, the medium ANS crude exhibited mean droplet diameter <70 μm, but was bimodal only for the 1:20 treatment. Bimodal distribution was not achieved with the heavy IFO, but droplet < 70 μm were observed for 1:20 warm waters, indicating poor dispersibility of the high viscosity oil even for jet releases. Results offer valuable information on the behavior and dispersibility of oils over a range of viscosity, DOR and environmental conditions. Findings have implications for fate and transport models, where DSD, chemistry and fluorescence are all impacted by release variables. This research was supported by the Bureau of Safety and Environmental Enforcement.

Indoor Air Quality Assessment and Study of Different VOC Contributions within a School in Taranto City, South of Italy

Children spend a large amount of time in school environments and when Indoor Air Quality (IAQ) is poor, comfort, productivity and learning performances may be affected. The aim of the present study is to characterize IAQ in a primary school located in Taranto city (south of Italy). Because of the proximity of a large industrial complex to the urban settlement, this district is one of the areas identified as being at high environmental risk in Italy. The study carried out simultaneous monitoring of indoor and outdoor Volatile Organic Compounds (VOC) concentrations and assessed different pollutants’ contributions on the IAQ of the investigated site. A screening study of VOC and determination of Benzene, Toluene, Ethylbenzene, Xylenes (BTEX), sampled with Radiello® diffusive samplers suitable for thermal desorption, were carried out in three classrooms, in the corridor and in the yard of the school building. Simultaneously, Total VOC (TVOC) concentration was measured by means of real-time monitoring, in order to study the activation of sources during the monitored days. The analysis results showed a prevalent indoor contribution for all VOC except for BTEX which presented similar concentrations in indoor and outdoor air. Among the determined VOC, Terpenes and 2-butohxyethanol were shown to be an indoor source, the latter being the indoor pollutant with the highest concentration.

Simultaneous determination of volatile organic compounds with a wide range of polarities in urine by headspace solid-phase microextraction coupled to gas chromatography/mass spectrometry.

Volatile organic compounds (VOCs) are ubiquitous environmental pollutants that have a high vapor pressure at room temperature. Some VOCs have been classified as carcinogenic to humans by the International Agency for Research on Cancer (IARC), because they can bind to DNA and cause cell mutations. Therefore, monitoring of VOCs in human urine is very important to evaluate the correlation between exposure to VOCs and human disease. We have developed an improved analytical method for the simultaneous determination of VOCs with a wide range of polarities in human urine samples by headspace solid-phase microextraction (HS-SPME) coupled to gas chromatography/mass spectrometry (GC/MS). In the improved method, a bi-polar carboxen-polydimethylsiloxane (CAR/PDMS) fiber was used for the optimized extraction of 15 VOCs with a wide range of polarities, including benzene, toluene, ethylbenzene, xylenes (BTEX), alkylbenzenes, cresols, and naphthalene, in human urine samples. Extracted VOCs from the human urine were effectively separated by GC using a mid-polarity column (DB-35, 35% phenylmethylpolysiloxane) and monitored by MS using extracted ion monitoring (EIM) mode. Under the optimized method, the linearity of the calibration curves was greater than 0.993. The limits of detection (LODs) at a signal-to-noise (S/N) ratio of 3 were 0.3-0.6ng/mL. The coefficients of variation were in the range of 0.1-9.7% for within-day variation and 0.2-14.2% for day-to-day variation. The method was shown to be rapid and simple for the simultaneous determination of VOCs with a wide range of polarities in human urine and it could be applied to monitoring and to biomedical investigations to check exposure to VOCs. Copyright © 2017 John Wiley & Sons, Ltd.

Screening of transition metal/oxide-impregnated ZSM-5 catalysts for deoxygenation of biomass oxygenates via direct methane intervention

ABSTRACTRemoval of oxygen from biomass (deoxygenation) is a significant challenge that needs to be overcome to effectively produce hydrocarbon-based biofuel. The present technology needs extraneous hydrogen (H2) to act as a proton donor, to effectively remove this oxygen. This work is geared toward finding an effective catalyst that accommodates the direct use of methane, instead of H2, for deoxygenation reactions. Here, we studied the impact of three oxides (Ga2O3, MoO3, Cr2O3) and two metals (Pt, Ni) impregnated (at 1, 2 and 5% loadings) on ZSM-5 support on furan conversion, benzene-toluene-ethylbenzene-xylenes (BTEX) selectivity, and coke formation when furan was catalytically pyrolyzed in methane and methane-free environments. The results indicate that Ga-, Pt- and Ni-based catalysts increase BTEX selectivity in a methane environment as opposed to methane-free conditions. The type of metal and the amount of loading had a significant impact on furan conversion as well. Ga/ZSM-5-based catalyst displayed the highest BTEX selectivity, while Ni/ZSM-5 resulted in the highest furan conversion. The results are significant since there is strong evidence of select catalysts’ ability to activate methane and in turn allow furan deoxygenation. This work paves the way to use methane (or natural gas) instead of H2 as a direct proton donor for deoxygenation reactions.

Exposure to chemical hazards in petrol pumps stations in Ahvaz City, Iran

ABSTRACTThe objective of this study was to assess the level of exposure to BTEX (benzene, toluene, ethylbenzene, xylenes) in petrol pump stations in Ahvaz City. Two of the biggest fuelling stations were selected randomly among total 12 fuel stations of Ahvaz City, Iran, during September 2013. Thirty air samples were taken from different positions in the fuelling stations and 15 samples were taken from the personal breathing zone of operators and of customers in fuelling stations. Measuring the ambient concentration of benzene, toluene, ethylbenzene, and xylenes was done according to the method advised by National Institute for Occupational Safety and Health (NIOSH) 1501. This study showed that the concentration of benzene was very high (compared with the Iranian occupational exposure limit [OEL] standard) in ambient air of petrol stations in Ahvaz, which is considered as a high risk to the health of workers. Controlling the level of benzene in petrol stations is necessary. A new designed petrol nozzle was proposed for this purpose.

Performance of different oxidants in the presence of oxisol: Remediation of groundwater contaminated by gasoline/ethanol blend

Abstract In this study, Na 2 S 2 O 8 , K 2 S 2 O 8 , H 2 O 2 , and CaO 2 were tested for the remediation of groundwater contaminated by a gasoline/ethanol blend. In fuel spills, groundwater acquires high organic carbon content and a considerable amount of BTEX (benzene, toluene, ethylbenzene, xylene), and can be treated using In Situ Chemical Oxidation. Batch tests were conducted to select the best oxidant, which establishes, in the presence of oxisol (soil rich in iron), the proper conditions for the generation of radicals. The results indicated that the H 2 O 2 added was scavenged in the process and that CaO 2 , which releases H 2 O 2 slowly, achieved the best removal results. However, this compound has low solubility, forms precipitates and increases pH to 12. Therefore, Na 2 S 2 O 8 was selected instead, once it achieved good removal results, worked at low pH values and had slow kinetics, making it suitable for groundwater remediation. Tests revealed that the concentration of iron in a ferriferous oxisol promotes proper oxidant activation, achieving 99% BTEX removal and 45% COD removal. GC–MS analysis of the oxidized samples showed the formation of intermediates (e.g. acetic acid and 1-acetic anhydride with formic acid) indicating the pathway of remediation. Despite such remarkable results, soil control sample achieved considerable DOC removal, suggesting that the use of ISCO may speed the remediation process, but the soil itself has a mechanism to degrade this kind of organic matter.

Measurement of volatile organic compounds (VOCs) in libraries and archives in Florence (Italy)

Indoor air samples from libraries and archives in Florence, Italy, were collected and analysed for a variety of volatile organic compounds. The aim was to perform a characterisation of the indoor air quality, and try to elucidate if there are VOCs that may cause or result from the determination of the cultural heritage institutions.All compounds of interest were regularly detected, with BTEXs (Benzene, Toluene, Ethylbenzene, Xylenes) being the most abundant and followed by cyclic volatile methylsiloxanes, aldehydes, terpenes and organic acids. The prevalence and qualitative characteristics, such as concentrations, profiles and indoor/outdoor ratios of BTEXs underline the important influence of the outdoor air infiltrations on the indoor air concentrations. Acetic acid that is a substance that can oxidise books and other exposed objects was detected at concentrations ranging between 1.04 and 18.9μgm−3, while furfural, that is a known marker of paper degradation, was constantly present at concentrations that ranged between 5.26 and 32.6μgm−3.This work shows the importance that indoor air quality monitoring campaigns can have in order to give early warning to cultural heritage institution managers about the impact that indoor air quality can have on exposed and/or preserved objects.

Improved treatment approach for the removal of aromatic compounds using polymeric beads in Fenton pretreatment and biological oxidation.

An improved approach based on the use of iron-doped polymeric beads (IPB) as Fenton catalyst in the pretreatment and biomass-doped polymeric bead (BPB) in the biological oxidation has been reported for the removal of different aromatic mixtures present as pollutants in the aqueous solutions. Degradation has been investigated at fixed loading of IPB as 2.5% weight basis and varying loading of hydrogen peroxide so as to understand the effect of oxidant loading on the extent of degradation. It has been observed that the maximum removal efficiency as 75.5, 81.4, and 59.1% was obtained for the benzene-toluene-naphthalene-xylene (BTNX), benzene-toluene-ethylbenzene-xylene (BTEX), and benzene-toluene-naphthalene-p-nitrophenol (BTNp-NP) mixtures, respectively, at a 40-min pretreatment and optimum pH of 3.5. The biodegradability index was also observed in the favorable range of 0.4 to 0.5 after the pretreatment at optimum H2O2 loading of 1.5gL-1. Maximum COD removal efficiency of 99.2, 99.3, and 99.6% was obtained using the biological oxidation treatment for 40h for the case of BTNX, BTEX, and BTNp-NP mixtures, respectively. Analysis of kinetic models revealed that degradation followed three distinct stages based on fitting of the three-stage model and BPB was found to be more efficient as compared to the primary activated sludge (PAS) and modified activated sludge (MAS). Reusability studies confirmed that both IPB and BPB were effective over many cycles giving stable performance during degradation without leaching of Fe3+ ions into the solution.

Концентрации бензола, толуола, этилбензола и о-ксилола в почвах и атмосферных осадках в городах Алматы и Астана

BTEX (benzene, toluene, ethylbenzene, xylene) is one of the most dangerous groups of organic toxicants in terms of emissions and risks to public health. BTEX are present in almost all technogenic and natural objects. The greatest risk to public health is caused by BTEX contamination of cities characterized by high population densities and emissions to the environment. The aim of this work was to determine the concentrations of benzene, toluene, ethylbenzene and o-xylene in samples of soils and atmospheric precipitations selected in the cities of Almaty and Astana. Screening and quantification of analytes was performed by gas chromatography - mass spectrometry. Solid-phase microextraction was used for sample preparation. In the soil samples collected in the cities of Almaty and Astana, the concentrations of analytes ranged from 29.9 to 455 ng/g for benzene, from 9.9 to 375 ng/g for toluene, from 1.8 to 386 ng/g for ethylbenzene, and from 2.4 to 217 ng/g for o-xylene. Concentrations of BTEX in samples of atmospheric precipitations varied in the range of 8.2-21.2 ng/g for benzene; 0.8-5.1 ng/g for toluene; 0.1-1.1 ng/g for ethylbenzene; and 0.2-0.5 ng/g for o-xylene. BTEX concentrations in analyzed soil samples were in average ten times higher than those measured in European cities.

Field Measurements of Gasoline Direct Injection Emission Factors: Spatial and Seasonal Variability.

Four field campaigns were conducted between February 2014 and January 2015 to measure emissions from light-duty gasoline direct injection (GDI) vehicles (2013 Ford Focus) in an urban near-road environment in Toronto, Canada. Measurements of CO2, CO, NOx, black carbon (BC), benzene, toluene, ethylbenzene-xylenes (BTEX), and size-resolved particle number (PN) were recorded 15 m from the roadway and converted to fuel-based emission factors (EFs). Other than for NOx and CO, the GDI engine had elevated emissions compared to the Toronto fleet, with BC EFs in the 73rd percentile, BTEX EFs in the 80-90th percentile, and PN EFs in the 75th percentile during wintertime measurements. Additionally, for three campaigns, a second platform for measuring PN and CO2 was placed 1.5-3 m from the roadway to quantify changes in PN with distance from point of emission. GDI vehicle PN EFs were found to increase by up to 240% with increasing distance from the roadway, predominantly due to an increasing fraction of sub-40 nm particles. PN and BC EFs from the same engine technology were also measured in the laboratory. BC EFs agreed within 20% between the laboratory and real-world measurements; however, laboratory PN EFs were an order of magnitude lower due to exhaust conditioning.

BTEX exposures in an area impacted by industrial and mobile sources: Source attribution and impact of averaging time

ABSTRACTThe impacts of emissions plumes from major industrial sources on black carbon (BC) and BTEX (benzene, toluene, ethyl benzene, xylene isomers) exposures in communities located >10 km from the industrial source areas were identified with a combination of stationary measurements, source identification using positive matrix factorization (PMF), and dispersion modeling. The industrial emissions create multihour plume events of BC and BTEX at the measurement sites. PMF source apportionment, along with wind patterns, indicates that the observed pollutant plumes are the result of transport of industrial emissions under conditions of low boundary layer height. PMF indicates that industrial emissions contribute >50% of outdoor exposures of BC and BTEX species at the receptor sites. Dispersion modeling of BTEX emissions from known industrial sources predicts numerous overnight plumes and overall qualitative agreement with PMF analysis, but predicts industrial impacts at the measurement sites a factor of 10 lower than PMF. Nonetheless, exposures associated with pollutant plumes occur mostly at night, when residents are expected to be home but are perhaps unaware of the elevated exposure. Averaging data samples over long times typical of public health interventions (e.g., weekly or biweekly passive sampling) misapportions the exposure, reducing the impact of industrial plumes at the expense of traffic emissions, because the longer samples cannot resolve subdaily plumes. Suggestions are made for ways for future distributed pollutant mapping or intervention studies to incorporate high time resolution tools to better understand the potential impacts of industrial plumes.Implications: Emissions from industrial or other stationary sources can dominate air toxics exposures in communities both near the source and in downwind areas in the form of multihour plume events. Common measurement strategies that use highly aggregated samples, such as weekly or biweekly averages, are insensitive to such plume events and can lead to significant under apportionment of exposures from these sources.

Migration of BTEX and phthalates from natural rubber latex balloons obtained from the Sri Lankan market.

The current study evaluates the migration of benzene, toluene, ethylbenzene, xylene (BTEX) and phthalates into artificial saliva from natural rubber latex (NRL) balloons available for sale in Sri Lanka. It was discovered that at least one BTEX compound migrated from almost all the brands. The migration of four phthalates; diethyl phthalate, dibutyl phthalate, di-isobutyl phthalate and butyl benzyl phthalate were also observed. Migratory levels of BTEX and phthalates in most of the balloon brands were above the permissible levels set by the European Union. Assessment of factors affecting the migratory levels indicated migration under active mouthing conditions and migration from the neck region of the balloons were significantly higher. The migratory levels were observed to decrease with storage time, and in certain brands the BTEX levels decreased below the permissible level. One-way ANOVA indicated no significant differences (p ≥ 0.05) in migratory levels of each individual compound within the same brand for both BTEX and phthalates. When compared among different brands, BTEX levels indicated significant differences (p ≤ 0.05), while phthalate levels were observed to not be significantly different (p ≥ 0.05). A significant difference was also observed (p ≤ 0.05) among the migratory levels of compounds under each test condition evaluated as factors affecting the migratory level. Furthermore, the solvent based colorants added to color the latex were found to be the source of BTEX and phthalates in the NRL balloons.