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.     

Indoor air quality for chemical and ultrafine particle contaminants from printers

There are various emission sources of chemical contaminants, such as volatile organic compounds (VOCs) and ozone and particulate matter. This report is a study into the indoor air of a room containing either a laser printer/ink-jet printer, and the air contaminations were monitored for VOCs, ozone and ultrafine particle. The result confirmed an increase in the concentration of ozone and ultrafine particle numbers in the printing processes of the printer. The emission of VOCs and ozone were measured by the use of a test chamber. The chamber concentrations of styrene, xylenes and ozone were increased in printing process of the laser printer, and pentanol was detected from the ink-jet printer. The results suggest that an office or residential printer may be a source of indoor air contamination. It is necessary for emission from printers to monitor not only VOCs and particle but also ultrafine particles and other contaminants in indoor air.     

Estimation of biogenic volatile organic compounds emissions in subtropical island--Taiwan

Elevated tropospheric ozone is harmful to human health and plants. It is formed through the photochemical reactions involving volatile organic compounds (VOCs) and nitrogen oxides (NO(x)). The elevated ozone episodes occur mainly in summer months in the United States, while the high-ozone episodes frequently occur during the fall in Taiwan. The unique landscape of Taiwan produces tremendous amounts of biogenic VOCs in the mountain regions that are adjacent to concentrated urban areas. The urban areas, in turn, generate prodigious amounts of anthropogenic emissions. Biogenic VOC emissions have direct influence on tropospheric ozone formation. To explore the air quality problems in Taiwan, this study attempts to develop a biogenic VOC emission model suitable for air quality applications in Taiwan. The emission model is based on the Biogenic Emissions Inventory System Version 2 and coupled with a detailed Taiwan land use database. The 1999 total Taiwan biogenic VOC emissions were estimated at 214,000 metric tons. The emissions of isoprene, monoterpenes, and other VOCs were about 37.2%, 30.4%, and 32.4% of total biogenic VOC emissions, respectively. The annual total biogenic VOC emission per unit area was more than two times the value of that in any European country, implying that detailed emissions estimates in any size of region will benefit the global biogenic emission inventories.     

Ozone reaction with clothing and its initiated VOC emissions in an environmental chamber

Human health is adversely affected by ozone and the volatile organic compounds (VOCs) produced from its reactions in the indoor environment. Hence, it is important to characterize the ozone‐initiated reactive chemistry under indoor conditions and study the influence of different factors on these reactions. This investigation studied the ozone reactions with clothing through a series of experiments conducted in an environmental chamber under various conditions. The study found that the ozone reactions with a soiled (human‐worn) T‐shirt consumed ozone and generated VOCs. The ozone removal rate and deposition velocity for the T‐shirt increased with the increasing soiling level and air change rate, decreased at high ozone concentrations, and were relatively unaffected by the humidity. The deposition velocity for the soiled T‐shirt ranged from 0.15 to 0.29 cm/s. The ozone‐initiated VOC emissions included C6–C10 straight‐chain saturated aldehydes, acetone, and 4‐OPA (4‐oxopentanal). The VOC emissions were generally higher at higher ozone, humidity, soiling of T‐shirt, and air change rate. The total molar yield was approximately 0.5 in most cases, which means that for every two moles of ozone removed by the T‐shirt surface, one mole of VOCs was produced.     

The effect of wet film thickness on VOC emissions from a finishing varnish

Finishing varnishes, a typical type of oil-based varnishes, are widely used to shine metal, wood trim and cabinet surfaces in Hong Kong. The influence of wet film thickness on volatile organic compound (VOC) emissions from a finishing varnish was studied in an environmental test chamber. The varnish was applied on an aluminium foil with three different wet film thickness (35.2, 69.9 and 107.3 microm). The experimental conditions were 25.0 degrees C, 50.0% relative humidity (RH) with an air exchange rate of 0.5 h(-1). The concentrations of the major VOCs were monitored for the first 10 h. The air samples were collected by canisters and analysed by gas chromatography/mass selective detector (GC/MSD). Six major VOCs including toluene, chlorobenzene, ethylbenzene, m,p-xylene, o-xylene and 1,3,5-trimethylbenzene were identified and quantified. Marked differences were observed for three different film thicknesses. VOC concentrations increased rapidly during the first few hours and then decreased as the emission rates declined. The thicker the wet film, the higher the VOC emissions. A model expression included an exponentially decreasing emission rate of varnish film. The concentration and time data measured in the chamber were used to determine the parameters of empirical emission rate model. The present work confirmed that the film thickness of varnish influenced markedly the concentrations and emissions of VOCs.     

Assessment of pollutant emissions from dry-process photocopiers

Processes involved in pollutant emissions from a dry-process photocopier have been investigated in a controlled room dynamic environmental chamber. Volatile organic compound (VOC) emissions occurred at a constant rate dependent on copy speed. However, VOC emission rates per copy were increased by increases in chamber temperature (e.g., a 20% increase resulted from increasing temperature from 23 degrees C to 32 degrees C) or changing from single- to double-sided operation (40% increase). Respirable particle emissions occurred under copier-idle mode (probably from residues in the machine) as well as with copying. No significant chamber sink effects were observed for VOCs or respirable particles. Small emissions of nitrogen dioxide, ozone and formaldehyde were observed but were difficult to interpret. A procedure for assessing pollutant emissions from photocopiers is recommended.     

Emission behavior of formaldehyde and TVOC from engineered flooring in under heating and air circulation systems

Formaldehyde and volatile organic compounds (VOCs) from the adhesive, flooring, and flooring with adhesive were measured using a desiccator, a 20-L chamber and a field and laboratory emission cell (FLEC). Flooring with an adhesive is similar to that used in construction was applied to a floor heating system and an air circulation system, and the surface temperature of the flooring was set to 20 °C, 26 °C and 32 °C. The rate of formaldehyde emission from the flooring was the highest at 32 °C using a desiccator and decreased with time. The formaldehyde and aldehyde emissions from the samples using a 20-L chamber and FLEC showed a similar tendency. The VOCs emission trends with the 20-L chamber and FLEC were similar. The rate of formaldehyde and TVOC emission determined using FLEC was higher than that determined using the 20-L chamber method. The flooring emitted primarily benzene, toluene, ethylbenzene, styrene, xylene, as well as some unknown VOCs. There was a strong correlation between formaldehyde and TVOC emission for the 20-L chamber and FLEC. Samples using a floor heating system showed higher formaldehyde emission than those using an air circulation system. The level of TVOC emission was higher from the samples using an air circulation system than those using the floor heating system.     

Characterization of ozone precursor volatile organic compounds in urban atmospheres and around the petrochemical industry in the Tarragona region

This paper reports the results of an assessment of volatile organic compound (VOCs) levels in ambient air in samples collected at urban and industrial sites in southern Catalonia, which is home to one of the most important petrochemical complexes in southern Europe. This study contains data from a total of 192 samples collected in 2007, from May to October, at six air pollution measurement stations within the area of influence of several chemical and petrochemical industrial plants. The ambient air concentrations of a group of 65 VOCs, some of them ozone precursors, were determined by active sampling into sorbent tubes, thermal desorption and gas chromatography-mass spectrometry. At the same time, several meteorological parameters were also recorded, and levels of NO, NO₂ and O₃ measured by the automatic stations, have been included in the study as well. Ambient air profiles of the different areas were studied, and the ozone formation dependent on VOCs and NO₂ levels was also analysed, taking into account the photochemical ozone creation potential (POCP) for different groups of VOCs.     

Evaluation of low-VOC latex paints

Four commercially available low-volatile organic compound (VOC) latex paints were evaluated as substitutes for conventional latex paints by assessing both their emission characteristics and their performance as coatings. Bulk analysis indicated that the VOC contents of all four paints tested were considerably lower than those of conventional latex paints. Low VOC emissions were confirmed by small chamber emission tests. However, significant emissions of several aldehydes, especially formaldehyde which is a hazardous air pollutant, were detected in emissions from two of the four paints. American Society for Testing and Materials (ASTM) methods were used to evaluate the hiding power, scrub resistance, washability, dry to touch and yellowness index. The results indicated that one of the four low-VOC paints tested showed performance equivalent or superior to that of a conventional latex paint used as control. It was concluded that low-VOC latex paint can be a viable option to replace conventional latex paints for prevention of indoor air pollution. However, paints marketed as "low-VOC" may still have significant emissions of some individual VOCs, and some may not have performance characteristics matching those of conventional latex paints.     

Atmospheric volatile organic compound measurements during the 1996 Paso del Norte Ozone Study

Ambient air VOC samples were collected at surface air quality monitoring sites, near sources of interest, and aloft on the US (El Paso) and Mexican (Ciudad Juárez) side of the border during a six-week period of the 1996 Paso del Norte Ozone Study. Samples were collected at five sites, three on the US side and two on the Mexican side, during nine intensive operation days when high ozone levels were forecast for the area. Six other sites were sampled to characterize up-wind, down-wind and other emission sources. Samples for determining source profiles were collected for rush hour traffic, propane-powered bus exhaust, automobile paint shop emissions, propane fuels, and industrial manufacturing in Cd. Juárez and a refinery in El Paso. Most samples were collected in electro-polished stainless steel canisters for determination of C2 to C(10+) hydrocarbons by GC-FID. Carbonyl samples were collected on DNPH impregnated cartridges at three surface sites during aircraft flights and analyzed by HPLC. This paper presents the spatial and temporal characteristics of VOC species concentrations and compositions to examine the differences and similarities of the various locations and time periods. Overall surface, total non-methane hydrocarbon values ranged from 0.1 to 3.4 ppmC with the highest concentrations being recorded in the morning and evening at five vehicle-dominated sites, three in Cd. Juárez and two in El Paso. Toluene in El Paso samples and propane, which is used as a cooking and transportation fuel in Cd. Juárez, were the most abundant hydrocarbons. The most abundant carbonyls were acetaldehyde, acetone and formaldehyde.     

Hydrocarbon source apportionment for the 1996 Paso del Norte Ozone Study

The 1996 Paso del Norte (PdN) ozone study was conducted to improve current understanding of the significant meteorological and air quality processes that lead to high concentrations of ozone in El Paso, Texas (USA) and Ciudad Juárez, Chihuahua (Mexico). Two-hour canister samples were collected five times daily at 05.00-07.00 h, 07.00-09.00 h, 09.00-11.00 h, 11.00-13.00 h, and 15.00-17.00 h MST during intensive study periods at one urban and one rural site on each side of the border. An automated gas chromatograph was operated at one site in central El Paso. Source profiles (the fractional chemical composition of emissions) from motor vehicles, gasoline, liquefied petroleum gas, and commercial natural gas were combined with source profiles from other studies for input to the Chemical Mass Balance (CMB) receptor model to apportion the measured non-methane hydrocarbons (NMHC) to sources. On-road vehicle emissions accounted for one-half to two-thirds of the NMHC in Ciudad Juárez and El Paso with the highest contributions occurring during the morning and afternoon commute periods. Emissions from diesel exhaust contributed approximately 2-3% of NMHC in Ciudad Juárez and less than 2% in El Paso. The average sum of liquid gasoline and gasoline vapor increased during the day in Ciudad Juárez from 2% at 06.00 h to approximately 12% at 16.00 h. Diurnal and day-of-the-week patterns in the liquid gasoline contributions are essentially identical to the corresponding patterns for motor vehicle exhaust, which suggest that a large fraction of the liquid gasoline contribution may be associated with tailpipe emissions rather than evaporative emissions from motor vehicles or industrial sources. Including the sum of the two sources put the upper limit for tailpipe contributions at 60-70% of NMHC.     

Characterization of Emissions from Liquid Fuel and Propane Open Burns

The effect of accidental fires are simulated to understand the response of items such as vehicles, fuel tanks, and military ordnance and to remediate the effects through re-design of the items or changes in operational procedures. The comparative combustion emissions of using jet propellant (JP-5) liquid fuel pools or a propane manifold grid to simulate the effects of accidental fires was investigated. A helium-filled tethered aerostat was used to maneuver an instrument package into the open fire plumes to measure CO, CO₂, fine particulate matter (PM_2.5), polycyclic aromatic hydrocarbons (PAHs), volatile organic compounds (VOCs), and elemental/organic/total carbon (EC/OC/TC). The results showed that all emissions except CO₂ were significantly higher from JP-5 burns than from propane. The major portion of the PM mass from fires of both fuels was less than 1 µm in diameter and differed in carbon content. The PM_2.5 emission factor from JP-5 burns (129 ± 23 g/kg Fuel_c) was approximately 150 times higher than the PM_2.5 emission factor from propane burns (0.89 ± 0.21 g/kg Fuel_c). The PAH emissions as well as some VOCs were more than one hundred times higher for the JP-5 burns than the propane burns. Using the propane test method to study flammability responses, the environmental impact of PM_2.5, PAHs, and VOCs would be reduced by 2300, 700, and 100 times per test, respectively.     

Emission Of Volatile And Semivolatile Organic Compounds From Waterborne Paints – The Effect Of The Film Thickness

A waterborne paint was applied to tin plated steel sheets with three different film thicknesses. The emission of volatile and semivolaile organic compounds ((S) VOCs) from the samples was measured in small climatic chambers under standard conditions over a two-week period. The purpose of the study was to evaluate the effect of the film thickness on the emission rate decay. First order decay models, including sink effects for the high boiling (S) VOCs, were fitted to the concentration versus time data. The results showed that the first order rate constants decrease with increasing film thickness. In uddition, the results indicated that the emissions of the (S)VOCs in the waterborne paint film seemed to be controlled by evaporation. The thicknesses of paint films used in climatic chamber tests to estimate emission rates for product compurison or emission prediction must be known in order to prevent erroneous conclusions     

Impact of varying area of polluting surface materials on perceived air quality

A laboratory study was performed to investigate the impact of the concentration of pollutants in the air on emissions from building materials. Building materials were placed in ventilated test chambers. The experimental set-up allowed the concentration of pollution in the exhaust air to be changed either by diluting exhaust air with clean air (changing the dilution factor) or by varying the area of the material inside the chamber when keeping the ventilation rate constant (changing the area factor). Four different building materials and three combinations of two or three building materials were studied in ventilated small-scale test chambers. Each individual material and three of their combinations were examined at four different dilution factors and four different area factors. An untrained panel of 23 subjects assessed the air quality from the chambers. The results show that a certain increase in dilution improves the perceived air quality more than a similar decrease in area. The reason for this may be that the emission rate of odorous pollutants increases when the concentration in the chamber decreases. The results demonstrate that, in some cases the effect of increased ventilation on the air quality may be less than expected from a simple dilution model.     

Long-term Emission of Volatile Organic Compounds from Waterborne Paints – Methods of Comparison

The emission of volatile organic compounds (VOCs) from five different waterborne paints was measured in small climatic chambers under standard conditions over a one-year period. The aims of the study were to evaluate the time emission profiles and to develop methods for comparison of different paints. The paints were applied to tin-plated steel sheets. VOCs were sampled on Tenax TA and analysed by thermal desorption and gas chromatography. The chamber concentrations increased rapidly during the first few hours and then decreased as the emission rates dropped. A model expression including an exponentially decreasing emission rate of the paint film, the air exchange rate, and a normalization of the film thickness was fitted to the concentration versus time data. The time required to reach a given emission rate was estimated and found suitable for comparison of the emission of VOCs from the paints. It was found that data sampled within three weeks or less may be sufficient to predict the emission of VOCs up to one year. Reduction of long-term emissions may be achieved most efficiently by (1) substituting a more -volatile VOC whose emission is controlled by evaporation for a less volatile VOC characterized by diffusion-controlled emission and (2) reducing the paint film thickness rather than reducing the initial VOC content of the paint.     

Seasonal and diurnal variations of volatile organic compounds (VOCs) in the atmosphere of Hong Kong

Ambient VOCs samples were collected at three locations (PolyU campus (PU), Kwun Tong (KT), Hok Tsui (HT)) in Hong Kong during the periods of November 2000-February 2001 and June 2001-August 2001. Also the concentrations of VOCs in Cross Harbor tunnel in Hong Kong were obtained in order to determine the vehicular sources of VOCs. Toluene was the most abundant VOC detected in Hong Kong. At the PU station, which is close to a main road, the concentrations of most VOCs were higher in summer than in winter. However, at the background location HT, the concentrations of all VOCs except tetrachloroethene were higher in winter than in summer. Regional physical dispersion/transportation and mixing depth may be the reasons for higher VOC concentrations in winter at HT. The BTEX (benzene:toluene:ethylbenzene:xylene) ratios of PU and KT during winter period were (1.9:10.1:1.0:1.8) and (1.9:10.4:1.0:1.5), and (0.9:8.3:1.0:2.2) and (0.8:29.6:1.0:1.8) for summer season, respectively. The xylene/ethylbenzene (X/E) ratio was used to assess the relative age of the air parcels in this study. The concentrations of VOCs in the atmosphere in Hong Kong were mainly affected by direct emissions from vehicles, evaporation of fuels, photochemical reactions and few industrial emissions. The BTEX ratio in the tunnel was 2:10.4:1:3.2. The BTEX ratios at PU and KT during the winter period were similar to that in tunnel (except for xylenes). The X/E ratio in the tunnel was higher than that in the ambient air. This indicated that the freshly emitted xylenes in the tunnel decayed at different rates from OH-oxidation in the atmosphere. Good BTEX correlations (r>0.8) were found at PU and KT in winter (**P<0.01). Vehicular exhaust was the dominant source at PU and KT stations, and less evaporation of fuel or additive occurred at low temperature in winter. Diurnal variations of mean BTEX concentrations at the roadside monitoring station (PU) showed two peaks associated with traffic density and vehicle type.     

Secondary VOC emissions from flooring material surfaces exposed to ozone or UV irradiation

Chemical reactions on the surface of building materials can lead to secondary emissions from these materials that influence indoor air quality. Many studies have been made on the physical processes that influence material emissions. However, there are only a few studies on secondary emissions resulting from exposure of building material surfaces to ozone or ultraviolet (UV) irradiation. Therefore, this study was aimed at elaborating on the emission of chemicals resulting from chemical reactions initiated by the exposure of the surface of flooring materials to ozone or UV irradiation. The laboratory tests were conducted to estimate gas-phase emissions from the flooring materials when they were exposed to ozone or various kinds of light irradiation (infrared, sunlight, UV-A and UV-B lamps). The infrared and sunlight lamps significantly increased the temperature of the test specimens and, in turn, increased the emission rate for various organic compounds. The flooring materials used in this study had been treated with UV-cured surface coatings during their manufacturing. As a result, when exposed to UV irradiation, chemical transformations occurred resulting in the emission of a number of secondary products, including formaldehyde, acetaldehyde, cyclohexanone and benzaldehyde. Ozone reacted with chemicals present in the flooring materials to increase the emission rates of formaldehyde and acetaldehyde. Hence, the exposure of ozone and UV irradiation increased the secondary emissions of formaldehyde, even though the low formaldehyde emission type of flooring material was employed.     

Emissions of volatile organic compounds from polymer-based consumer products: Comparison of three emission chamber sizes

The ISO 16000 standard series provide guidelines for emission measurements of volatile organic compounds (VOCs) from building materials. However, polymer-based consumer products such as toys may also release harmful substances into indoor air. In such cases, the existing standard procedures are unsuitable for official control laboratories due to high costs for large emission testing chambers. This paper aims at developing and comparing alternative and more competitive methods for the emission testing of consumer products. The influence of the emission chamber size was investigated as smaller chambers are more suited to the common size of consumer products and may help to reduce the costs of testing. Comparison of the performance of a 203 L emission test chamber with two smaller chambers with the capacity of 24 L and 44 mL, respectively, was carried out by using a polyurethane reference material spiked with 14 VOCs during the course of 28 days. The area-specific emission rates obtained in the small chambers were always similar to those of the 203 L reference chamber after a few hours. This implies that smaller chambers can provide at least useful numbers on the extent of polymer-based consumer product emissions into indoor air, thereby supporting meaningful exposure assessments.     

Determination of formaldehyde emission with field and laboratory emission cell (FLEC)--recovery and correlation to the chamber method

The formaldehyde emission from wood-based building materials is usually determined in large chambers at a defined temperature, humidity and ventilation rate. In this article, a simpler method, the Field and Laboratory Emission Cell (FLEC), is described for determination of the formaldehyde emission and it is compared with the traditional chamber method. The formaldehyde from FLEC is collected on a silicagel cartridge impregnated with 2,4-dinitrophenylhydrazine (DNPH) and analysed with HPLC. The FLEC is easier to operate, requires a smaller sample, fewer analyses and is also more flexible than the chamber method. The emissions from different parts of a sample can be measured. Another advantage is that the equipment can be used to determine the volatile organic compounds (VOCs) emission at the same time. The FLEC method gives a good correlation to the chamber method for different building products. It also gives a good recovery. An average recovery of 98% was achieved, when two different FLEC-cells were tested with known formaldehyde sources with emissions of 0.06-0.7 mg/m2h.     

Some local environmental effects on mercury emission and absorption at a soil surface

The purpose of this study was to quantify effects of some local environmental variables on the soil surface exchanges of total gaseous mercury (TGM), under controlled conditions. A dynamic flux chamber with a Tekran mercury analyzer was used to quantify TGM emissions from, and absorption by, a clean, fine sandy loam soil with very low mercury content inside of a building and in a low TGM environment, outside. Simultaneous measurements of mercury flux, air and soil temperatures, ozone concentration, humidity, soil moisture and solar radiation were made. Controlled applications of water were made to change soil H2O content and measure the response of mercury flux. Air-soil exchanges were highly dependent on soil temperature (r2 = 0.78) and the mercury concentration gradient between the TGM in the soil pores and the ambient TGM above the soil surface (r2 = 0.98 for absorption and r2 = 0.408 for emissions). Correlations with air temperature and ozone levels are explained by the relationships of these variables with soil temperature. No detectable correlation was found with solar radiation or humidity. Wet soil maintained higher rates of soil TGM emission and decreased soil absorption. Emissions increased with increasing soil H2O, peaked at approximately field capacity, and then decreased slightly until saturation.