Exhaust ventilation in attached garages improves residential indoor air quality

Previous research has shown that indoor benzene levels in homes with attached garages are higher than homes without attached garages. Exhaust ventilation in attached garages is one possible intervention to reduce these concentrations. To evaluate the effectiveness of this intervention, a randomized crossover study was conducted in 33 Ottawa homes in winter 2014. VOCs including benzene, toluene, ethylbenzene, and xylenes, nitrogen dioxide, carbon monoxide, and air exchange rates were measured over four 48‐hour periods when a garage exhaust fan was turned on or off. A blower door test conducted in each garage was used to determine the required exhaust fan flow rate to provide a depressurization of 5 Pa in each garage relative to the home. When corrected for ambient concentrations, the fan decreased geometric mean indoor benzene concentrations from 1.04 to 0.40 μg/m³, or by 62% (P<.05). The garage exhaust fan also significantly reduced outdoor‐corrected geometric mean indoor concentrations of other pollutants, including toluene (53%), ethylbenzene (47%), m,p‐xylene (45%), o‐xylene (43%), and carbon monoxide (23%) (P<.05) while having no impact on the home air exchange rate. This study provides evidence that mechanical exhaust ventilation in attached garages can reduce indoor concentrations of pollutants originating from within attached garages.     

Effects of energy retrofits on Indoor Air Quality in multifamily buildings

We assessed 45 multifamily buildings (240 apartments) from Finland and 20 (96 apartments) from Lithuania, out of which 37 buildings in Finland and 15 buildings in Lithuania underwent energy retrofits. Building characteristics, retrofit activities, and energy consumption data were collected, and Indoor Air Quality (IAQ) parameters, including carbon monoxide (CO), nitrogen dioxide (NO₂), formaldehyde (CH₂O), selected volatile organic compounds (benzene, toluene, ethylbenzene, and xylenes (BTEX), radon, and microbial content in settled dust were measured before and after the retrofits. After the retrofits, heating energy consumption decreased by an average of 24% and 49% in Finnish and Lithuanian buildings, respectively. After the retrofits of Finnish buildings, there was a significant increase in BTEX concentrations (estimated mean increase of 2.5 µg/m³), whereas significant reductions were seen in fungal (0.6‐log reduction in cells/m²/d) and bacterial (0.6‐log reduction in gram‐positive and 0.9‐log reduction in gram‐negative bacterial cells/m²/d) concentrations. In Lithuanian buildings, radon concentrations were significantly increased (estimated mean increase of 13.8 Bq/m³) after the retrofits. Mechanical ventilation was associated with significantly lower CH₂O concentrations in Finnish buildings. The results and recommendations presented in this paper can inform building retrofit studies and other programs and policies aimed to improve indoor environment and health.     

Atmospheric levels of BTEX compounds during the 2008 Olympic Games in the urban area of Beijing

The hourly concentrations of BTEX (Benzene, Toluene, Ethylbenzene, m,p-Xylene and o-Xylene) in the urban area of Beijing were measured during July-October 2008, covering the periods of the 2008 Olympic Games and Paralympic Games. The atmospheric BTEX were pre-concentrated on Tenax-TA tubes, and analyzed by GC-PID (Gas Chromatography with Photo Ionization Detector) after thermal desorption. During the games, the mean daytime concentrations of benzene, toluene, ethylbenzene, m,p-xylene and o-xylene were 2.37, 3.97, 1.92, 3.51 and 1.90 μg/m³, respectively, and were 52.8%, 63.9%, 56.4%, 56.8% and 46.9%, respectively lower than those after the games. The significantly positive correlation between BTEX and CO as well as the ratio of benzene/toluene suggested that the vehicle exhaust was the major source of BTEX during the whole investigated period. The extremely high ratios of ethylbenzene to m,p-xylene (E/X) were mainly observed at noontime in haze days, indicating that photochemical reactions were highly active under these typical days.     

Indoor air quality,air exchange rates,and radioactivity in new built temporary houses following the Great East Japan Earthquake in Minamisoma,Fukushima

This study measured air exchange rates, indoor concentrations of aldehydes and volatile organic compounds (VOCs), and radioactivity levels at 19 temporary houses in different temporary housing estate constructed in Minamisoma City following the Great East Japan Earthquake. The 19 surveyed houses represented all of the companies assigned to construct temporary houses in that Minamisoma City. Data were collected shortly after construction and before occupation, from August 2011 to January 2012. Mean air exchange rates in the temporary houses were 0.28/h, with no variation according to housing types and construction date. Mean indoor concentrations of formaldehyde, acetaldehyde, toluene, ethylbenzene, m/p‐xylene, o‐xylene, styrene, p‐dichlorobenzene, tetradecane, and total VOCs (TVOCs) were 29.2, 72.7, 14.6, 6.35, 3.05, 1.81, 7.29, 14.3, 8.32, and 901 μg/m³, respectively. The levels of acetaldehyde and TVOCs exceeded the indoor guideline (48 μg/m³) and interim target (400 μg/m³) in more than half of the 31 rooms tested. In addition to guideline chemicals, terpenes (α‐pinene and d‐limonene) and acetic esters (butyl acetate and ethyl acetate) were often detected in these houses. The indoor radiation levels measured by a Geiger–Müller tube (Mean: 0.22 μSv/h) were lower than those recorded outdoors (Mean: 0.42 μSv/h), although the shielding effect of the houses was less than for other types of buildings.     

Levels and sources of volatile organic compounds in homes of children with asthma

Many volatile organic compounds (VOCs) are classified as known or possible carcinogens, irritants, and toxicants, and VOC exposure has been associated with the onset and exacerbation of asthma. This study characterizes VOC levels in 126 homes of children with asthma in Detroit, Michigan, USA. The total target VOC concentration ranged from 14 to 2274 μg/m³ (mean = 150 μg/m³; median = 91 μg/m³); 56 VOCs were quantified; and d‐limonene, toluene, p, m‐xylene, and ethyl acetate had the highest concentrations. Based on the potential for adverse health effects, priority VOCs included naphthalene, benzene, 1,4‐dichlorobenzene, isopropylbenzene, ethylbenzene, styrene, chloroform, 1,2‐dichloroethane, tetrachloroethene, and trichloroethylene. Concentrations varied mostly due to between‐residence and seasonal variation. Identified emission sources included cigarette smoking, solvent‐related emissions, renovations, household products, and pesticides. The effect of nearby traffic on indoor VOC levels was not distinguished. While concentrations in the Detroit homes were lower than levels found in other North American studies, many homes had elevated VOC levels, including compounds that are known health hazards. Thus, the identification and control of VOC sources are important and prudent, especially for vulnerable individuals. Actions and policies to reduce VOC exposures, for example, sales restrictions, improved product labeling, and consumer education, are recommended.     

Concentrations and risk assessment of selected monoaromatic hydrocarbons in buses and bus stations of Hangzhou, China

Air pollution surveys of ten selected monoaromatic hydrocarbons (MAHCs) were conducted in buses and bus stations in Hangzhou, China. The mean concentrations of MAHCs in the air of buses and bus stations were 95.9 and 36.5 μg/m³, respectively, of which toluene was the highest in all the sampling sites. Mean concentrations of all MAHCs in buses were statistically higher than those nearby bus stations (p < 0.05). MAHCs concentrations in buses largely depend on vehicle conditions (including vehicle type, fuel type, interior decoration, etc.) and traffic conditions (mainly traffic density). Among the investigated buses, microbuses had the highest MAHCs level, while electric buses had the lowest. Buses driven in downtown had the highest MAHCs level, followed by those in suburban areas and tourist areas. The mean concentration ratio of toluene to benzene was 2.1 ± 0.9, indicating that vehicle emission was the dominant source of MAHCs. Interior decorations, such as painting and surface coating, could also contribute to the MAHCs in the buses. The mean lifetime carcinogenic risks for passengers and bus drivers were 1.11 × 10^− 5 and 4.00 × 10^− 5, respectively, which were way above the limit set by USEPA. The health risk caused by MAHCs in bus microenvironment should be cautioned.     

On-site passive flux sampler measurement of emission rates of carbonyls and VOCs from multiple indoor sources

In indoor environments with high levels of air pollution, it is desirable to remove major sources of emissions to improve air quality. In order to identify the emission sources that contribute most to the concentrations of indoor air pollutants, we used passive flux samplers (PFSs) to measure emission rates of carbonyl compounds and volatile organic compounds (VOCs) from many of the building materials and furnishings present in a room in a reinforced concrete building in Tokyo, Japan. The emission flux of formaldehyde from a desk was high (125 μg/m²/h), whereas fluxes from a door and flooring were low (21.5 and 16.5 μg/m²/h, respectively). The emission fluxes of toluene from the ceiling and the carpet were high (80.0 and 72.3 μg/m²/h, respectively), whereas that from the flooring was low (9.09 μg/m²/h). The indoor and outdoor concentrations of formaldehyde were 61.5 and 8.64 μg/m³, respectively, and those of toluene were 43.2 and 17.5 μg/m³, respectively. The air exchange rate of the room as measured by the perfluorocarbon tracer (PFT) method was 1.84/h. Taking into consideration the area of the emission sources, the carpet, ceiling, and walls were identified as the principal emission sources, contributing 24%, 20%, and 22% of the formaldehyde, respectively, and 22%, 27%, and 14% of the toluene, respectively, assuming that the emission rate from every major emission sources could be measured. In contrast, the door, the flooring, and the desk contributed little to the indoor levels of formaldehyde (1.0%, 0.54%, and 4.1%, respectively) and toluene (2.2%, 0.31%, and 0.85%, respectively).     

Modelling and kinetic aspects of a BTEX contaminated air-treating biofilter

In this study, the overall performance of a biofilter was evaluated in terms of its elimination capacity by using 3-D mesh techniques. The overall results indicate that the agreement between experimental data and model predictions is excellent for benzene, toluene, ethylbenzene and o-xylene (BTEX). In this study, the maximum removal rate (r _max) values for BTEX were 0.0117, 0.0126, 0.0081 and 0.0146 g m^–3 h^–1, and the half-saturation constant (K_S ) values were calculated to be 0.269, 0.297, 0.156 and 0.394 g m^–3, respectively. For this system, the coefficients of determination (r ²) of BTEX compounds were greater than 0.97. The BTEX concentration profiles along the depth were also determined using a convection–diffusion reactor (CDR) model. The sums of squares of the errors (SSEs) of BTEX were 0.0078, 0.0059, 0.0129 and 0.0269, respectively, with r ² values greater than 0.99 for all four compounds at low concentrations.     

Biodegradation of monoaromatic hydrocarbons in aquifer columns amended with hydrogen peroxide and nitrate

The ability of indigenous microorganisms to degrade benzene, toluene, ethylbenzene and xylenes (BTEX) in laboratory scale flow-through aquifer columns was tested separately with hydrogen peroxide (110 mg/l) and nitrate (330 mg/l as NO₃⁻) amendments to air-saturated influent nutrient solution. The continuous removal of individual components from all columns relative to the sterile controls provided evidence for biodegradation. In the presence of hydrogen peroxide, the indigeneous microorganisms degraded benzene and toluene (> 95%), meta- plus para-xylene (80%) and ortho-xylene (70%). Nitrate addition resulted in 90% removal of toluene and 25% removal of ortho-xylene. However, benzene, ethylbenzene, meta- and para-xylene concentrations were not significantly reduced after 42 days of operation. Following this experiment, low dissolved oxygen (< 1 mg/l) conditions were initiated with the nitrate-amended column influent in order to mimic contaminated groundwater conditions distal from a nutrient injection well. Toluene continued to be effectively degraded (> 90%), and more than 25% of the benzene, 40% of the ethylbenzene, 50% of the meta- plus para-xylenes and 60% of the ortho-xylene were removed after several months of operation.     

Volatile organic compounds in 169 energy-efficient dwellings in Switzerland

Exposure to elevated levels of certain volatile organic compounds (VOCs) in households has been linked to deleterious health effects. This study presents the first large-scale investigation of VOC levels in 169 energy-efficient dwellings in Switzerland. Through a combination of physical measurements and questionnaire surveys, we investigated the influence of diverse building characteristics on indoor VOCs. Among 74 detected compounds, carbonyls, alkanes, and alkenes were the most abundant. Median concentration levels of formaldehyde (14 μg/m³), TVOC (212 μg/m³), benzene (<0.1 μg/m³), and toluene (22 μg/m³) were below the upper exposure limits. Nonetheless, 90% and 50% of dwellings exceeded the chronic exposure limits for formaldehyde (9 μg/m³) and TVOC (200 μg/m³), respectively. There was a strong positive correlation among VOCs that likely originated from common sources. Dwellings built between 1950s and 1990s, and especially, those with attached garages had higher TVOC concentrations. Interior thermal retrofit of dwellings and absence of mechanical ventilation system were associated with elevated levels of formaldehyde, aromatics, and alkanes. Overall, energy-renovated homes had higher levels of certain VOCs compared with newly built homes. The results suggest that energy efficiency measures in dwellings should be accompanied by actions to mitigate VOC exposures as to avoid adverse health outcomes.     

Ambient air levels of volatile organic compounds (VOC) and nitrogen dioxide (NO2) in a medium size city in Northern Spain

Ambient concentrations of volatile organic compounds (VOC) and nitrogen dioxide (NO₂) were measured by means of passive sampling at 40 sampling points in a medium-size city in Northern Spain, from June 2006 to June 2007. VOC and NO₂ samplers were analysed by thermal desorption followed by gas chromatography/mass-selective detector and by visible spectrophotometry, respectively. Mean concentrations of benzene, toluene, ethylbenzene, xylenes, propylbenzene, trimethylbenzenes, and NO₂ were 2.84, 13.26, 2.15, 6.01, 0.59, 1.32 and 23.17 µg m^− 3 respectively, and found to be highly correlated. Their spatial distribution showed high differences in small distances and pointed to traffic as the main emission source of these compounds. The lowest levels of VOC and NO₂ occurred during summer, owing to the increase in solar radiation and to lower traffic densities. Mean concentrations of benzene and NO₂ exceeded the European limits at some of the monitored points.     

Indoor and outdoor air concentrations of BTEX and determinants in a cohort of one-year old children in Valencia, Spain

BTEX is the commonly used term for a group of toxic compounds (benzene, toluene, ethyl benzene, ortho-xylene and meta- and para-xylene), some of which, most notably benzene, are known carcinogens. The aim of this study is to measure the BTEX levels both inside and outside the homes of 352 one-year old children from the Valencia cohort of the INMA study (Spain) and to analyze the determinants of these levels. Passive samplers were used to measure BTEX levels during a 15 day period and a questionnaire was administered to gather information on potentially associated factors (sociodemographics, residential conditions, and lifestyle). The average concentrations of benzene, toluene, ethyl benzene, ortho-xylene, and meta- and para-xylene were 0.9, 3.6, 0.6, 0.6, and 1.0 μg/m³, respectively. On average, the indoor levels of all the compounds were approximately 2.5 times higher than those observed outdoors. Factors associated with higher BTEX concentrations inside the home were being the child of a mother of non-Spanish origin, living in a house that had been painted within the last year, living in an apartment, and not having air conditioning. Higher outdoor concentrations of BTEX depend on the residence being situated in a more urban zone, being located within the city limits, having living in a building with more than one story, residing in an area with a greater frequency of traffic, and the season of the year in which the sample was taken. The data thus obtained provide helpful information not only for implementing measures to reduce exposure to these pollutants, but also for evaluating the relation between such exposure and possible health risks for the children in the cohort.     

Spatial modelling of gaseous emissions from two municipal solid waste dump sites

This paper reports the spatial modelling of gaseous emissions from two municipal solid waste dump sites to determine exposure to landfill gases. The AERMOD modelling software and the Mexican Biogas Model were used, with information from nearby meteorological stations for the period 2015–2016. It was observed that, at one of the dump sites, gas emissions reach populated areas, but in concentrations too low to be detected by the olfactory pathway (benzene <5 µg/m³, toluene and xylene <50 µg/m³). At the second dump site, concentrations are greater; there are no population settlements close by. The highest concentrations of benzene, toluene, xylene and hydrogen sulphide are found within, or around, the dump sites, reaching levels greater than 38 μg/m³ for benzene, 770 μg/m³ for toluene and 237 μg/m³ for xylene.     

Air exchange rates and migration of VOCs in basements and residences

Basements can influence indoor air quality by affecting air exchange rates (AERs) and by the presence of emission sources of volatile organic compounds (VOCs) and other pollutants. We characterized VOC levels, AERs, and interzonal flows between basements and occupied spaces in 74 residences in Detroit, Michigan. Flows were measured using a steady‐state multitracer system, and 7‐day VOC measurements were collected using passive samplers in both living areas and basements. A walk‐through survey/inspection was conducted in each residence. AERs in residences and basements averaged 0.51 and 1.52/h, respectively, and had strong and opposite seasonal trends, for example, AERs were highest in residences during the summer, and highest in basements during the winter. Airflows from basements to occupied spaces also varied seasonally. VOC concentration distributions were right‐skewed, for example, 90th percentile benzene, toluene, naphthalene, and limonene concentrations were 4.0, 19.1, 20.3, and 51.0 μg/m³, respectively; maximum concentrations were 54, 888, 1117, and 134 μg/m³. Identified VOC sources in basements included solvents, household cleaners, air fresheners, smoking, and gasoline‐powered equipment. The number and type of potential VOC sources found in basements are significant and problematic, and may warrant advisories regarding the storage and use of potentially strong VOCs sources in basements.     

Biological and environmental exposure monitoring of volatile organic compounds among nail technicians in the Greater Boston area

Nail technicians are exposed to volatile organic compounds (VOCs) from nail products, but no studies have previously measured VOC biomarkers for these workers. This study of 10 nail technicians aimed to identify VOCs in nail salons and explore relationships between air concentrations and biomarkers. Personal and area air samples were collected using thermal desorption tubes during a work shift and analyzed using gas chromatography/mass spectrometry (GC/MS) for 71 VOCs. Whole blood samples were collected pre‐shift and post‐shift, and analyzed using GC/MS for 43 VOCs. Ventilation rates were determined using continuous CO₂ measurements. Predominant air VOC levels were ethyl methacrylate (median 240 µg/m³), methyl methacrylate (median 205 µg/m³), toluene (median 100 µg/m³), and ethyl acetate (median 639 µg/m³). Blood levels were significantly higher post‐shift than pre‐shift for toluene (median pre‐shift 0.158 µg/L and post‐shift 0.360 µg/L) and ethyl acetate (median pre‐shift <0.158 µg/L and post‐shift 0.510 µg/L); methacrylates were not measured in blood because of their instability. Based on VOCs measured in these seven nail salons, we estimated that emissions from Greater Boston area nail salons may contribute to ambient VOCs. Ventilation rates did not always meet the ASHRAE guideline for nail salons. There is a need for changes in nail product formulation and better ventilation to reduce VOC occupational exposures.     

Real-time air monitoring of occupational exposures to particulate matter among hairdressers in Maryland: A pilot study

Hairdressers are exposed to particulate matter (PM), a known air pollutant linked to adverse health effects. Still, studies on occupational PM exposures in hair salons are sparse. We characterized indoor air PM concentrations in three salons primarily serving an African/African American (AA) clientele, and three Dominican salons primarily serving a Latino clientele. We also assessed the performance of low-cost sensors (uRAD, Flow, AirVisual) by comparing them to high-end sensors (DustTrak) to conduct air monitoring in each salon over 3 days to quantify work shift concentrations of PM_2.5, respirable PM (RPM), and PM₁₀. We observed high spatial and temporal variability in 30-min time-weighted average (TWA) RPM concentrations (0.18–5518 μg/m³). Readings for the uRAD and AirVisual sensors were highly correlated with the DustTrak (R² = 0.90–0.99). RPM 8-hour TWAs ranged from 18 to 383 µg/m³ for AA salons, and 9–2115 µg/m³ for Dominican salons. Upper 95th percentiles of daily RPM exposures ranged from 439 to 2669 µg/m³. The overall range of 30-min TWA PM_2.5 and PM₁₀ concentrations was 0.13–5497 and 0.36-,541 μg/m³, respectively. Findings suggest that hairdressers could be overexposed to RPM during an 8-hour shift. Additional comprehensive monitoring studies are warranted to further characterize temporal and spatial variability of PM exposures in this understudied occupational population.     

The impact of biogas and fuelwood use on institutional kitchen air quality in Kampala,Uganda

Experts have suggested that microscale biogas systems offer a source of renewable energy that improves indoor air quality, but such impacts have not been directly measured. This study documented cooking behaviors and measured 2.5‐μm particulate matter (PM_2.5), carbon monoxide (CO), and sulfur dioxide (SO₂) concentrations within 14 institutional kitchens in Kampala, Uganda, that prepare meals using biogas (n=5), a mixture of biogas and fuelwood (n=3), and fuelwood (n=6). Small institutions (10‐30 people) with biogas kitchens had 99% lower concentrations of PM_2.5 (21 μg/m³) than fuelwood kitchens (3100 μg/m³). Larger institutions (>100 people) had biogas systems that produced insufficient gas and relied on fuelwood to meet over 90% of their energy needs. PM_2.5 concentrations in these biogas‐firewood kitchens were equivalent to concentrations in fuelwood kitchens. Although concentrations of hydrogen sulfide (H₂S) in biogas were as high as 2000 ppm, 75% of systems had undetectable H₂S levels (<100 ppm) in the biogas. Kitchens using biogas with high H₂S had correspondingly higher SO₂ concentrations in the kitchen air. However, even the highest SO₂ concentration in biogas kitchens (150 μg/m³) was lower than SO₂ concentration in fuelwood kitchens (390 μg/m³). The results suggest that biogas systems can offer air quality improvements if sized properly for energy demands.     

Investigation of volatile organic compounds in office buildings in Bangkok,Thailand: Concentrations,sources, and occupant symptoms

To conserve energy, office buildings with air-conditioning systems in Thailand are operated with a tight thermal envelope. This leads to low fresh-air ventilation rates and is thought to be partly responsible for the sick building syndrome symptoms reported by occupants. The objectives of this study are to measure concentrations and to determine sources of 13 volatile organic compounds (VOCs) in office buildings with air-conditioning systems in the business area of Bangkok. Indoor and outdoor air samples from 17 buildings were collected on Tenax-TA^™ sorbent tubes and analyzed for individual VOCs by thermal desorption-gas chromatography/mass spectrometry (TD–GC/MS). Building ventilation was measured with a constant injection technique using hexafluorobenzene as a tracer gas. The results show that the VOC concentrations varied significantly among the studied buildings. The two most dominant VOCs were toluene and limonene with average concentrations of 110 and 60.5 μg m⁻³, respectively. A Wilcoxon sum rank test indicated that the indoor concentrations of aromatic compounds and limonene were statistically higher than outdoor concentrations at the 0.05 level, while the indoor concentrations of chlorinated compounds were not. Indoor emission factors of toluene and limonene were found to be highest with the average values of 80.9 and 18.9 μg m⁻² h⁻¹, respectively. Principal component analysis was applied to the emission factors of 13 VOCs, producing three components based on source similarities. Furthermore, a questionnaire survey investigation and field measurements of building air exchange pointed to indoor air complaints related to inadequate ventilation.     

Unexpected increase in indoor pollutants after the introduction of a smoke‐free policy in a correctional center

Correctional centers (prisons) are one of the few non‐residential indoor environments where smoking is still permitted. However, few studies have investigated indoor air quality (IAQ) in these locations. We quantified the level of inmate and staff exposure to secondhand smoke, including particle number (PN) count, and we assessed the impact of the smoking ban on IAQ. We performed measurements of indoor and outdoor PM_2.5 and PN concentrations, personal PN exposure levels, volatile organic compounds (VOCs), and nicotine both before and after a complete indoor smoking ban in an Australian maximum security prison. Results show that the indoor 24‐h average PM_2.5 concentrations ranged from 6 (±1) μg/m³ to 17 (±3) μg/m³ pre‐ban. The post‐ban levels ranged from 7 (±2) μg/m³ to 71 (±43) μg/m³. While PM_2.5 concentrations decreased in one unit post‐ban, they increased in the other two units. Similar post‐ban increases were also observed in levels of PN and VOCs. We describe an unexpected increase of indoor pollutants following a total indoor smoking ban in a prison that was reflected across multiple pollutants that are markers of smoking. We hypothesise that clandestine post‐ban smoking among inmates may have been the predominant cause.     

Urinary BTEX, MTBE and naphthalene as biomarkers to gain environmental exposure profiles of the general population

The aim of this work was to evaluate urinary benzene, toluene, ethylbenzene, m+p-xylene, o-xylene (BTEX), methyl tert-butyl ether (MTBE), ethyl tert-butyl ether (ETBE), and naphthalene (NAP) as biomarkers of exposure to environmental pollutants. Personal air and urine samples from 108 subjects belonging to the Italian general population were compared. Urinary profiles were obtained by headspace gas chromatography-mass spectrometry. BTEX, MTBE, ETBE and NAP median airborne exposures during a 5-h sampling were 4.0, 25.3, 3.8, 9.3, 3.4, 3.4, < 0.8, and 3.4 µg/m³, respectively. Meanwhile, median urinary levels, as geometric means of three determinations were: 122, 397, 74, 127, 43, 49, < 15, and 46 ng/L, respectively. Urinary benzene and toluene concentrations were 4.6- and 1.2-fold higher in smokers than in non-smokers. For most chemicals, significant positive correlations between airborne exposure (log-transformed) and the corresponding biological marker (log-transformed) were found, with Pearson's r values for correlation, ranging from 0.228 to 0.396. Multiple linear regression analysis showed that the urinary level of these chemicals was influenced by personal airborne exposure, urinary creatinine, and urinary cotinine, with R² 0.733 for benzene. Urinary chemicals are useful biomarkers of environmental exposure. Given the ease of rapidly obtaining urine samples, they represent a non-invasive alternative to blood chemical analysis. The possibility of obtaining urinary exposure profiles makes this method an appealing tool for environmental epidemiology.