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PubMed2005

Emissions of VOCs at urban petrol retail distribution centres in India (Delhi and Mumbai).

Air pollution has assumed gigantic proportion killing almost half a million Asians every year. Urban pollution mainly comprises of emissions from buses, trucks, motorcycle other forms of motorized transport and its supporting activities. As Asia's cities continue to expand the number of vehicles have risen resulting in greater pollution. Fugitive emissions from retail distribution center in urban area constitute a major source. Petrol vapours escape during refueling adding pollutants like benzene, toluene, ethylbenzene and xylene to ambient air. This paper discusses a study on fugitive emissions of Volatile Organic Compounds (VOC) at some refueling station in two metropolitan cities of India, i.e., Mumbai and Delhi. Concentration of VOCs in ambient air at petrol retail distribution center is estimated by using TO-17 method. Concentration of benzene in ambient air in Delhi clearly shows the effect of intervention in use of petroleum and diesel fuel and shift to CNG. Chemical Mass Balance (CMB) model is used to estimate source contributions. At Delhi besides diesel combustion engines, refueling emissions are also major sources. At Mumbai evaporative emissions are found to contribute maximum to Total VOC (TVOC) concentration in ambient air.

Air Pollutants↗
PubMed2006

Characterization of volatile organic compounds (VOCs) and their sources in the air of Izmir, Turkey.

Air samples were collected in Izmir, Turkey at two (suburban and urban) sites during three sampling programs in 2002 and 2004 to determine the ambient concentrations of several monoaromatic, chlorinated and oxygenated volatile organic compounds (VOCs). Samples were analyzed for 60 VOCs using gas chromatography/mass spectrometry and 28 compounds were detected in most samples. On the average, urban air VOC concentrations were about four times higher than those measured at the suburban site. Toluene (40.6%) was the most abundant compound in suburban site and was followed by benzene (7.4%), o,m-xylene (6.5%), and 1,2-dichloroethane (5.1%). In urban site, toluene (30.5%), p-xylene (14.9%), o,m-xylene (11.4%), and ethyl benzene (7.2%) were the dominating compounds in summer. In winter, toluene (31.1%), benzene (23.9%), 1,2-dichloroethane (9.5%), and o,m-xylene (8.2%) were the most abundant compounds. Receptor modeling (positive matrix factorization) has been performed to estimate the contribution of specific source types to ambient concentrations. Six source factors (gasoline vehicle exhaust, diesel vehicle exhaust+residential heating, paint production/application, degreasing, dry cleaning, and an undefined source) were extracted from the samples collected in the urban site. Three source factors (gasoline vehicle exhaust, diesel vehicle exhaust, and paint production/application) were identified for the suburban site.

Air Pollutants↗
PubMed2004

Chemical composition of major VOC emission sources in the Seoul atmosphere.

This paper describes a chemical analysis of volatile organic compounds (VOCs) for five emission sources in Seoul. The source categories included motor vehicle exhaust, gasoline evaporation, paint solvents, natural gas and liquefied petroleum gas (LPG). These sources were selected because they have been known to emit significant quantities of VOCs in the Seoul area (more than 5% of the total emission inventory). Chemical compositions of the five emission sources are presented for a group of 45 C2-C9 VOCs. Motor vehicle exhaust profiles were developed by conducting an urban tunnel study. These emissions profiles were distinguished from the other emission profiles by a high weight percentage of butanes over seasons and propane in the wintertime. It was found that this is due to the wide use of butane-fueled vehicles. To obtain gasoline vapor profiles, gasoline samples from five major brands for each season were selected. The brands were blended on the basis of the marketshare of these brands in Seoul area. Raoult's law was used to calculate gasoline evaporative compositions based on the liquid gasoline compositions. The measured and estimated gasoline vapor compositions were found to be in good agreement. Vehicle and gasoline evaporation profiles were made over seasons because of the seasonal change in their compositions. Paint solvent emissions profiles were produced based on a product-use survey and sales figures. These profiles are a composite of four major oil-based paints and thinning solvent. The source profile of natural gas was made on a methane-free basis. It was found that Ethane and propane were the most abundant compounds accounting for 95% of the natural gas composition. LPG was largely composed of propane and ethane and the remaining components were minor contributors.

Air Pollutants↗
PubMed2006

Testing VOC emission measurement techniques in wood-coating industrial processes and developing a cost-effective measurement methodology.

Availability of reliable emission measurements of concentrated volatile organic compounds (VOCs) bear great significance in facilitating the selection of a feasible emission abatement technique. There are numerous methods, which can be used to measure VOC emissions, however, there is no single method that would allow sampling of the whole range of volatile organics. In addition, research efforts are usually directed to the development of measuring VOCs in diluted concentrations. Therefore, there is a need for a novel measurement method, which can give reliable results while entailing simple operations and low costs. This paper represents a development effort of finding a reliable measurement procedure. A methodology is proposed and used to measure solvent emissions from coating processes.

Air Pollutants↗
PubMed2006

Relationship between VOC and NOx emissions and chemical production of tropospheric ozone in the Aburrá Valley (Colombia).

Relationship between volatile organic compounds (VOC) and nitrogen oxides (NOx) emissions and the chemical production of tropospheric ozone is studied through mathematical simulation. The study is applied to the Aburrá Valley, in the Colombian Andes, which is a practically unknown area from the point of view of ozone formation. The model used for this application is the European modelling of atmospheric constituents (EUMAC) zooming model (EZM) which consists of a mesoscale prognostic model (MEMO, mesoscale meteorological model) and a chemical reaction model (MUSE, multiscale for the atmospheric dispersion of reactive species), coupled to the chemical mechanism EMEP (European monitoring and evaluation program). The analysis is performed for a real episode that was characterized by high ozone production and that happened during the 23rd and 24th December, 1999 in Medellín (Colombia). From this real scenario, a sensitivity analysis has been carried out in order to assess the influence of VOC and NOx amounts on ozone production and to extract some conclusions for future ozone abatement policies in Andean regions. As far as ozone air quality is concerned, it is shown that in order to keep current levels the emphasis must be put to avoid increasing NOx emissions, or alternatively, to augment VOC emissions in order to have a high VOC/NOx ratio.

Air Pollutants↗
PubMed2006

Using UV pretreatment to enhance biofiltration of mixtures of aromatic VOCs.

Mixtures of airborne toluene and o-xylene, two relatively recalcitrant volatile organic compounds (VOCs), were treated effectively using integrated UV-biofiltration. The set-up consisted of a biofilter receiving UV-pretreated stream and a reference biofilter receiving no pretreatment. Experimental conditions included UV fluences of 6 and 12 mJcm(-2) as well as air flow rates of 6.3 and 9.4 Lmin(-1), corresponding to biofilter empty bed retention times (EBRTs) of 45 and 30s, respectively. The inlet concentration of organics (toluene and o-xylene) ranged between 70 and 650 mg(carbon)m(-3). The UV-biofilter consistently provided removal efficiencies of greater than 95% over the range of toluene and o-xylene inlet concentrations. Also, the coupled UV-biofiltration system provided up to 60% additional contaminant removal compared to the sum of that offered by UV and reference biofilter, demonstrating the synergistic effect of UV on biofilter performance. The UV photooxidation partially oxidized a fraction of toluene and o-xylene into water soluble and more biodegradable intermediates, such as acetaldehyde and formaldehyde, which were readily removed in the downstream biofilter. These intermediates along with up to 20ppmv ozone, formed through the photolysis of oxygen by 185 nm UV, contributed to the enhanced degradation of parent VOCs in the biofilter as well as the absence of any inhibitory effects of the VOCs on one another. Also, the presence of ozone helped control the growth of excess biofilm in the UV-coupled biofilter. While the standalone biofilter showed significant pressure drop increase (of up to 14 mm H(2)Om(-1) of the bed) over the course of experiment, the UV-coupled biofilter maintained a relatively low pressure drop of less than 3 mmH(2)Om(-1) of the bed.

Air Pollutants↗
PubMed2004

Source apportionment of ambient VOCs in Delhi City.

Source apportionment using chemical mass balance (CMB) model was carried using a data set of 360 four hourly samples collected at 15 locations of five categories namely residential, commercial, industrial, traffic intersections and petrol pumps during August 2001-July 2002 in Delhi. The results indicate that emissions from diesel internal combustion engines dominate in Delhi. Vehicular exhaust and evaporative emissions also contribute significantly to VOCs in ambient air. Emission of VOCs associated with sewage sludge was also found to contribute to VOCs in Delhi's air. This points to the fact that open defecation and leaking sewage manholes are a problem in all categories of locations.

Air Pollutants↗
PubMed1997

Airway symptoms among house painters in relation to exposure to volatile organic compounds (VOCS)--a longitudinal study.

The increased use of water-based paint (WBP) for indoor application during the last decade has drastically changed the exposure conditions for Swedish house painters. WBP has a lower emission of volatile organic compounds (VOCs) than solvent-based paint (SBP), but contains more reactive compounds, such as biocides, glycol ethers, and other high molecular solvents. The aim of this study was to compare the incidence of airway symptoms and self-reported asthma in house painters with a different degree of use of WBP and SBP. The incidence of seven general airway symptoms, and three work-related symptoms, was analysed by means of a self-administered questionnaire, in a cohort of 207 house painters followed from 1989 to 1992. Different airway symptoms were compared with clinical information obtained by a methacholine challenge test and dynamic spirometry in a selected subgroup of 44 painters. Information on the degree of use of SBP and WBP was used to estimate the total exposure to volatile organic compounds (TVOC) for each individual. In total, 175 men in the cohort worked as painters during the study period. No increase of asthma or respiratory symptoms was observed among those 50 painters with a pure exposure to WBP (estimated TVOC 1-3 mg m-3). Most painters (N = 125) had a mixed exposure to SBP and WBP, the main source of the TVOC being the limited use of SBP. WBP was perceived as less irritative than SBP, but complaints on airway irritation from WBP increased during the study period. The most pronounced increase of airway irritation in relation to both SBP and WBP, was observed among those 35 painters with the highest solvent exposure (estimated TVOC 100-380 mg m-3). An increase of respiratory symptom index and shortness of breath, in relation to estimated TVOC exposure was also observed. Selection effects were detected. Painters leaving their job during the study period had more non-specific hyper-reactivity symptoms, and more airway irritation from WBP, as compared to painters remaining at their occupation. Our study indicates that VOC emissions from SBPs may contribute to the development of respiratory symptoms and airway irritation. We found no increase of respiratory symptoms among painters exposed only to WBPs. There were, however, indications that VOC exposure from WBPs may cause airway irritation in some subjects. Because of selection effects, cross-sectional studies on respiratory symptoms in relation to occupational exposure to paint emissions may be inconclusive.

Adult↗
PubMed2003

VOC concentration characteristics in Southern Taiwan.

The field investigations were conducted at four air quality monitoring sites in Southern Taiwan during northeasterly prevailing monsoon to collect 160 data sets on volatile organic compounds (VOCs) to evaluate the ozone formation potential (OFP) of the air mass. The gas chromatograph and high performance liquid chromatography analyzed 58 VOCs and two aldehydes, respectively. Among the four sampling sites, the order of the five VOC classes based on the reactivity approach was different from the concentration-based method. Alkenes as well as aromatics provided a major contribution for the OFP. The relative ranking of the species at the four sites were quite dissimilar. Toluene was the most in abundance at each site. The most abundant species at the windward and leeward sites was different. The reactivity of the air mass at the leeward sites showed a similar pattern and had higher reactivity than the windward sites. Comparisons of the two ratios, xylene/benzene and toluene/benzene were used to assess the relative age of the air parcels and provide evidence of transport.

Air Movements↗
PubMed1997

Evaluation of a novel assay of potential toxicity/neurotoxicity of carpet emissions (VOCs) in mice.

A private testing laboratory utilizing the whole-body plethysmograph/head-only exposure apparatus outlined in the respiratory irritation assay ASTM E981-84, along with a novel exposure regimen, has reported neurotoxic effects and mortality in mice exposed to relatively low levels of volatile organic compounds (VOCs) emitted from a number of consumer products. This methodology was evaluated by exposing groups of mice, including unrestrained and sham-treated animals, to VOCs generated from a sample of carpet reported to be neurotoxic using the modified assay. General toxicological (haematological measurements, organ weights, gross pathology, histopathology) and specific neurotoxicity (functional observations, body temperature, histopathology of nervous tissues) parameters were evaluated. No effects related to exposure to carpet VOCs were observed in the mice. However, despite careful handling, a number of effects were observed which were attributed to the repeated restraint of mice in the ASTM E981 apparatus. These included a number of minor physical injuries, decreased body weights, altered thymus weights, compression damage to the liver and haemorrhage of the pituitary gland. It was concluded that the modification of the original ASTM E981 methodology may result in physical injuries and stress which may significantly affect any evaluation of toxicity and neurotoxicity in treated animals and result in inaccurate conclusions.

Air Pollutants↗
PubMed2000

Removal mechanisms of VOCs in an activated sludge process.

This study investigated the factors in plant operating parameters effecting volatile organic compound (VOC) removal and elucidated each individual mechanism in an activated sludge process (ASP). The results suggest that stripping increase with an increase in Henry's law constant with the exception of toluene, which differed because of the effect of biodegradation competition. The emission rate can be controlled by increasing the active biomass concentration (X(b)) in the aeration basin, hydraulic retention time (HRT), and oxygen transfer efficiency (OTE). Increasing X(b) enhances total VOC removal and biodegradation, which reduces the fraction of the stripping removal. Longer HRT can reduce stripping removal significantly if other variables such as oxygen requirement and OTE are held constant. For the same volatile compound, a process with higher air-to-water ratio requires a higher active biomass concentration to reduce stripping removal. Increasing OTE decreases the air-to-water ratio requirement, which reduces the gas-phase transfer of VOCs into the atmosphere. The results show a reasonable agreement between measured and predicted stripping values.

Biodegradation, Environmental↗
PubMed2002

Structural investigation of catalyst deactivation of Pt/SDB for catalytic oxidation of VOC-containing wastewater.

The stability of styrene-divinyl benzene copolymer (SDB)-supported Pt (Pt/SDB) catalysts for destruction of volatile-organic-compound (VOC) in wastewater was examined. The test reaction was wet oxidation of water-containing aliphatic alcohol and formaldehyde at 140 degrees C and 90 psig for 40 h. The catalytic performance tests indicated that activity of the Pt/SDB catalysts could be maintained for VOC concentration of 3 wt.%, whereas the catalysts deactivated rapidly for 10 wt.% VOC containing wastewater. In order to investigate the nature of catalyst deactivation, extended X-ray absorption fine structure (EXAFS) and X-ray absorption near edge (XANES) spectroscopy were used to characterize the fresh and used catalysts. After the reaction, there is no oxidation of Pt clusters observed in EXAFS and XANES spectroscopy suggesting that the oxidation reaction takes places via the adsorbed oxygen. The spectroscopy results further indicated that deactivation of the catalysts were mainly caused by the increase of Pd particle size. After the reaction, the Pt-Pt coordination number has no significant change for the 3 wt.% wastewater whereas increase from 5.6 to 6.2 for 10 wt.% wastewater. Combined with the fact that the catalysts fractured during the reactions, we suggested that Pt agglomeration was mainly caused by thermal migration of the metal clusters.

Catalysis↗
PubMed2000

Carbon isotope effects resulting from equilibrium sorption of dissolved VOCs.

To accurately interpret isotopic data obtained for volatile organic compounds (VOCs) dissolved in groundwater systems, the isotopic effects of subsurface processes must be understood. Previous work has demonstrated that volatilization and dissolution of BTEX and chlorinated ethene compounds are not significantly isotopically fractionating. This study characterized the carbon isotopic effects of equilibrium sorption of perchloroethylene, trichloroethylene, benzene, and toluene to both graphite and activated carbon directly in batch experiments over a range of 10-90% sorption. Results demonstrate that, over this range, equilibrium sorption of these VOCs to graphite and activated carbon does not result in significant carbon isotopic fractionation within the +/-0.5% accuracy and reproducibility associated with compound-specific isotope analysis. This implies that the isotopic values of dissolved VOCs will not be significantly affected by equilibrium sorption in the subsurface. Therefore, isotopic analysis has potential to be used in the field to differentiate between mass losses due to isotopically fractionating processes such as biodegradation versus mass loss due to nondegradative processes.

Journal Article↗
PubMed2001

Concentrations and sources of VOCs in urban domestic and public microenvironments.

Concentrations of 15 VOCs including 1,3-butadiene, benzene, and styrene were measured in a wide range of urban microenvironments, viz: homes, offices, restaurants, pubs, department stores, coach and train stations, cinemas, libraries, laboratories, perfume shops, heavily trafficked roadside locations, buses, trains, and automobiles. For most target VOCs-including 1,3-butadiene and benzene-mean concentrations at heavily trafficked roadside locations were exceeded by those in automobiles and were comparable to those in pubs and train stations. With regard to indoor-outdoor relationships in homes, this study revealed higher mean indoor concentrations, no correlation between simultaneously measured indoor and outdoor concentrations, and significantly different patterns of diurnal variation. Thus-in poorly ventilated buildings-indoor emission source strength is considered a more significant influence on VOC concentrations than infiltration of outdoor air. In the six smoking homes studied, environmental tobacco smoke (ETS) was found to make a substantial contribution to concentrations of 1,3-butadiene. This finding was based on the significantly higher concentrations detected in smoking compared to nonsmoking homes, the significant correlation between 1,3-butadiene concentrations and those of 3-ethenylpyridine (an ETS marker), factor analysis, and the results of a source apportionment exercise based on ratios of 1,3-butadiene to 3-ethenylpyridine.

Air Pollution, Indoor↗
PubMed2003

Using a passive multilayer sampler for measuring detailed profiles of gas-phase VOCs in the unsaturated zone.

The purpose of this study was to test in the laboratory the performance of a passive multilayer sampler (MLS) for obtaining detailed profiles of gas-phase volatile organic compounds (VOCs) in unsaturated sediments. The MLS is essentially a chain of isolated, cylindrical stainless steel dialysis cells filled with distilled water and closed with membranes at both ends. The sampling principle is based on passive equilibration of the unsaturated zone gas phase with water in the cells. Using trichloroethene (TCE) as a model VOC, and after testing the required equilibration time in the laboratory (about 50 h), results of a large container (210 L) experiment show that TCE concentrations obtained by the MLS deployed inside a well screen corresponded very well to the profile obtained by dialysis cells buried in the sediment. A field profile taken at the saturated-unsaturated interface region of a VOC-contaminated area using the MLS shows steep TCE concentration gradients (1119 microg TCE/L-air/cm) in the gas phase of the unsaturated zone just above the water table.

Environmental Monitoring↗
PubMed2002

VOCs fate and partitioning in vegetation: use of tree cores in groundwater analysis.

Analysis of tree cores collected from contaminated sites has shown that concentrations of VOCs in cores are related to groundwater concentrations. However, initial research was highly qualitative. To better understand the relationship of groundwater VOC concentrations to measured VOCs in tree cores, detailed understanding of contaminant behavior in vegetation is required. Work presented here investigates the interaction, with focus on the chlorinated solvents trichloroethylene, 1,1,2,2-tetrachloroethane, and carbon tetrachloride. The sorption and desorption partitioning of these compounds between air and woody biomass were investigated. Partitioning coefficients were determined for cores of trunks of large trees and smaller stem cuttings. The internal partitioning of these compounds between the transpiration stream and the woody biomass within the tree was also determined for cores. The partitioning coefficients of the compounds between air, water, and biomass of tree cores and trunks were related to the physicochemical characteristics of contaminants, mainly the Henry's law constant and vapor pressure. These partitioning coefficients relate the contaminants' concentration in the bulk solution and analyzed headspace of vials and therefore can be utilized to quantify the fate of contaminants in natural settings and in phytoremediation systems. Tissue analysis and determination of partitioning coefficients may provide an effective way to estimate the concentration of compounds in the transpiration stream and in the soil or groundwater in a noninvasive, extremely rapid, and cost-effective manner.

Adsorption↗
PubMed2004

Susceptibility of residential wells to VOC and nitrate contamination.

Water quality of residential wells is vital to public health and a complex issue for regulatory agencies. South Carolina, a typical southeastern rural state, has no required testing of residential well water quality after initial well construction. This study used site-selection criteria to identify susceptible residential wells based on a combination of geologic vulnerability and potential contaminant loading. Geologic vulnerability was defined as increased probability of contaminants being transported from the land surface into the groundwater based on geological properties. As a surrogate for potential general contaminant loading, wells were located within 800 m of an EPA Toxics Release Inventory facility reporting VOC emissions, thus sampling was nonrandom. Seventy private residential wells were sampled for volatile organic compounds (VOCs) and nitrate-nitrogen (NO3-N) and analyzed using gas chromatography/mass spectrometry and the cadmium reduction method, respectively. Geographic Information Systems (GIS) was used to quantify four explanatory variables that affect well susceptibility to nitrate: population density, land cover, local relief (percent slope), and soil texture. VOCs were detected in 11 wells, and two sites exceeded the MCL for 1,1-dichloroethylene (36.1 microg/L) and trichloroethylene (9.0 microg/L). Elevated NO3-N (defined as > or = 1.0 mg/L) was measured in 20 wells. Logistic regression identified grassland/cultivated land cover as a variable that significantly increased the probability of NO3-N contamination (p = 0.003). Using easily accessible databases to identify factors that increase the probability of groundwater pollution could lead to more effective programs for locating residential wells that are susceptible to contamination. Increased monitoring of well water quality, as is being considered in some states, is warranted to reduce potential human exposure to contaminated drinking water.

Agriculture↗
PubMed2006

Measured concentrations of VOCs in several non-residential microenvironments in the United States.

Individuals spend about 25% of their time in non-residential indoor microenvironments. For some of these microenvironments, particularly stores and restaurants, exposures to volatile organic compounds (VOCs), have not been well characterized. In the Boston Exposure Assessment in Microenvironments (BEAM) study, sampling using scripted activities was conducted in stores, restaurants, and transportation in the summer of 2003 and winters of 2004 and 2005. A suite of VOCs including hydrocarbons, several chlorinated compounds, and aldehydes was analyzed. Nine store types were sampled using a composite design to enable a greater number of stores to be visited. Stores had higher concentrations of formaldehyde, toluene, ethylbenzene, xylenes, and styrene than other microenvironments, particularly in certain store types. Geometric mean formaldehyde levels were highest in the housewares stores, at 53 microg/m3 (95% CI = 43, 66). Geometric mean toluene levels were highest in multipurpose stores, at 76 microg/m3 (95% CI = 50, 118). The levels observed in stores were several times higherthan levels found in transportation microenvironments, and indicate strong indoor sources. In contrast, benzene did not have significantly higher levels in stores than typically found outdoors. Concentrations of formaldehyde and benzene, ethylbenzene, xylenes, and styrene were strongly influenced by the presence of smoking in the dining microenvironment. Chloroform levels were higher in restaurants than in other microenvironments, with a geometric mean of 1.1 microg/m3 (95% CI = 0.7, 1.8). The VOC concentrations found in stores and restaurants in this study are a potentially important source of exposure for sensitive individuals or people who work in these microenvironments.

Air Pollution, Indoor↗