Contaminant levels,source strengths,and ventilation rates in California retail stores

This field study measured ventilation rates and indoor air quality in 21 visits to retail stores in California. Three types of stores, such as grocery, furniture/hardware stores, and apparel, were sampled. Ventilation rates measured using a tracer gas decay method exceeded the minimum requirement of California's Title 24 Standard in all but one store. Concentrations of volatile organic compounds (VOCs), ozone, and carbon dioxide measured indoors and outdoors were analyzed. Even though there was adequate ventilation according to standard, concentrations of formaldehyde and acetaldehyde exceeded the most stringent chronic health guidelines in many of the sampled stores. The whole‐building emission rates of VOCs were estimated from the measured ventilation rates and the concentrations measured indoor and outdoor. Estimated formaldehyde emission rates suggest that retail stores would need to ventilate at levels far exceeding the current Title 24 requirement to lower indoor concentrations below California's stringent formaldehyde reference level. Given the high costs of providing ventilation, effective source control is an attractive alternative.     

Indoor and outdoor concentrations of RSP, NO2 and selected volatile organic compounds at 32 shoe stalls located near busy roadways in Seoul, Korea

It is suspected that persons who work in indoor environments near busy roadways are exposed to elevated levels of air pollutants during working hours. This study evaluated the potential exposure and source contribution associated with traffic-related air pollution for workers (polishers and repairmen) in shoe stalls from each of 32 districts during working hours in Seoul, Korea. The shoe stalls have been located at very close distances to the busy roadways. In this study, shoe stall workers could be exposed to high levels of respirable suspended particulate (RSP), nitrogen dioxide (NO(2)) and volatile organic compounds (VOCs) from outdoor sources such as traffic exhaust, as well as indoor sources in the shoe stalls such as dust on the shoes, portable gas ranges, organic solvents, adhesives and shoe polish. Compounds of particular note included indoor mean concentrations of benzene, toluene, m/p-xylene and o-xylene were 0.732, 6.777, 4.080 and 1.302 mg/m(3), respectively, in all shoe stalls. Mean indoor/outdoor ratios for toluene and m/p-xylene concentrations were 54.52 and 20.84, respectively. The contribution of vehicle exhaust emissions to indoor air quality of shoe stalls was identified by means of correlating the relationships between simultaneously measured air pollutant concentrations indoors and outdoors. Unlike RSP and NO(2), indoor VOCs concentrations of shoe stalls mainly originated from indoor sources vs. outdoor sources.     

The MERMAID study: indoor and outdoor average pollutant concentrations in 10 low‐energy school buildings in France

Indoor air quality was characterized in 10 recently built energy‐efficient French schools during two periods of 4.5 days. Carbon dioxide time‐resolved measurements during occupancy clearly highlight the key role of the ventilation rate (scheduled or occupancy indexed), especially in this type of building, which was tightly sealed and equipped with a dual‐flow ventilation system to provide air refreshment. Volatile organic compounds (VOCs) and inorganic gases (ozone and NO₂) were measured indoors and outdoors by passive techniques during the occupied and the unoccupied periods. Over 150 VOC species were identified. Among them, 27 species were selected for quantification, based on their occurrence. High concentrations were found for acetone, 2‐butanone, formaldehyde, toluene, and hexaldehyde. However, these concentrations are lower than those previously observed in conventional school buildings. The indoor/outdoor and unoccupied/occupied ratios are informative regarding emission sources. Except for benzene, ozone, and NO₂, all the pollutants in these buildings have an indoor source. Occupancy is associated with increased levels of acetone, 2‐butanone, pentanal, butyl acetate, and alkanes.     

Indoor/outdoor relationships of carbon monoxide and oxides of nitrogen in domestic homes with roadside, urban and rural locations in a central Indian region

Indoor air quality (IAQ) has been a matter of public concern these days whereas air pollution is normally monitored outdoors as part of obligations under the National air quality strategies. Much little is known about levels of air pollution indoors. Simultaneous measurements of indoor and outdoor carbon monoxide (CO) and oxides of nitrogen (NO and NO2) concentrations were conducted at three different environments, i.e. rural, urban and roadside in Agra, India, using YES - 205 multigas monitor during the winter season, i.e. October 2002-February 2003. A statistical correlation analysis of indoor concentration levels with outdoor concentrations was carried out. CO was maximum at roadside locations with indoor concentrations 2072.5 +/- 372 p.p.b. and outdoor concentrations 1220 +/- 281 p.p.b. (R2 = 0.005). Oxides of nitrogen were found maximum at urban site; NO concentration was 385 +/- 211 and 637 +/- 269 p.p.b. for indoors and outdoors respectively (R2 = 0.90792), where as NO2 concentration was 255 +/- 146 p.p.b. for indoors and 460 +/- 225 p.p.b. for outdoors (R2 = 0939464). Although indoor concentration at all the houses of the three sites have a positive correlation with outdoor concentration, CO variation indoors was very less due to outdoor sources. An activity schedule of inside and outside these homes were also prepared to see its influence and concentrations of pollutants. As standards for indoor air were not available for the Indian conditions these were compared with the known standards of other countries, where as outdoor concentrations were compared with the standards given by the Central Pollution Control board, which shows that indoor concentrations of both NO(x) and CO lie below permissible limits but outdoor concentrations of NO(x) cross the standard limits. PRACTICAL IMPLICATIONS: 'India currently bears the largest number of indoor air pollution (IAP) related health problems in world. An estimated 500,000 women & children die in India each year due to IAP-related cause--this is 25% of estimated IAP-related deaths worldwide. This study will be useful for policy makers, health related officials, academicians and Scientists who have interest in countries of developing world'.     

Real-time characterization of aerosol particle composition,sources and influences of increased ventilation and humidity in an office

Most of human exposure to atmospheric pollutants occurs indoors, and the components of outdoor aerosols may have been changed in the way before reaching indoor spaces. Here we conducted real-time online measurements of mass concentrations and chemical composition of black carbon and the non-refractory species in PM_2.5 in an occupied office for approximately one month. The open-close windows and controlled dampness experiments were also performed. Our results show that indoor aerosol species primarily originate from outdoors with indoor/outdoor ratio of these species typically less than unity except for certain organic aerosol (OA) factors. All aerosol species went through filtration upon transport indoors. Ammonium nitrate and fossil fuel OA underwent evaporation or particle-to-gas partitioning, while less oxidized secondary OA (SOA) underwent secondary formation and cooking OA might have indoor sources. With higher particulate matter (PM) mass concentration outdoors than in the office, elevated natural ventilation increased PM exposure indoors and this increased exposure was prolonged when outdoor PM was scavenged. We found that increasing humidity in the office led to higher indoor PM mass concentration particularly more oxidized SOA. Overall, our results highlight that indoor exposure of occupants is substantially different from outdoor in terms of mass concentrations and chemical species.     

Carbonyl levels in indoor and outdoor air in Mexico City and Xalapa,Mexico

Carbonyl compounds in air were measured at two houses, three museums, and two offices. All sites lacked air-conditioning systems. Although indoor and outdoor air was measured simultaneously at each site, the sites themselves were sampled in different dates. Mean concentrations were higher in indoor air. Outdoor means concentrations of acetone were the highest in all sites, ranging from 12 to 60 microg m(-3). In general, formaldehyde and acetaldehyde had similar mean concentrations, ranging from 4 to 32 and 6 to 28 microg m(-3), respectively. Formaldehyde and acetone mean indoor concentrations were the highest, ranging from 11 to 97 and 17 to 89 microg m(-3), respectively, followed by acetaldehyde with 5 to 47 microg m(-3). Formaldehyde and acetaldehyde had the highest mean concentration in the offices where there were smokers. Propionaldehyde and butyraldehyde concentrations did not show definite differences between indoor and outdoor air. In general, the highest outdoor and indoor hourly concentrations were observed from 10:00 to 15:00 h. Mean indoor/outdoor ratios of carbonyls exceeded 1. Formaldehyde and acetaldehyde risks were higher in smoking environments.     

Control strategies for sub-micrometer particles indoors: model study of air filtration and ventilation

The effects of air filtration and ventilation on indoor particles were investigated using a single-zone mathematical model. Particle concentration indoors was predicted for several I/O conditions representing scenarios likely to occur in naturally and mechanically ventilated buildings. The effects were studied for static and dynamic conditions in a hypothetical office building. The input parameters were based on real-world data. For conditions with high particle concentrations outdoors, it is recommended to reduce the amount of outdoor air delivered indoors and the necessary reduction level can be quantified by the model simulation. Consideration should also be given to the thermal comfort and minimum outdoor air required for occupants. For conditions dominated by an indoor source, it is recommended to increase the amount of outdoor air delivered indoors and to reduce the amount of return air. Air filtration and ventilation reduce particle concentrations indoors, with the overall effect depending on efficiency, location and the number of filters applied. The assessment of indoor air quality for specific conditions could be easily calculated by the model using user-defined input parameters.     

Volatile organic pollutants in new and established buildings in Melbourne, Australia

Volatile organic compounds (VOCs) within new and established buildings have been determined and factors significant to their presence have been identified. In established dwellings, total volatile organic compound (TVOC) concentrations were low, but were approximately four times higher than in outdoor air, showing a dominant effect of indoor sources. The presence of attached garages, site contamination and 'faulty' wool carpet were associated with higher indoor pollution. In three dwellings, unidentified sources of benzene were indicated. Much higher VOC concentrations were observed in new or renovated buildings, persisting above "baseline" levels for several weeks, concentration decay rate correlating with VOC molecular volume, indicating emissions were limited by material diffusion processes. VOC and formaldehyde emission decays in a new dwelling occurred by a double-exponential source model. This shows that persistent low levels of volatile organic pollutants in established dwellings can occur due to long-term emissions from building materials.     

Volatile organic compounds in fourteen U.S. retail stores

Retail buildings have a potential for both short‐term (customer) and long‐term (occupational) exposure to indoor pollutants. However, little is known about volatile organic compound (VOC) concentrations in the retail sector and influencing factors, such as ventilation, in‐store activities, and store type. We measured VOC concentrations and ventilation rates in 14 retail stores in Texas and Pennsylvania. With the exception of formaldehyde and acetaldehyde, VOCs were present in retail stores at concentrations well below health guidelines. Indoor formaldehyde concentrations ranged from 4.6 ppb to 67 ppb. The two mid‐sized grocery stores in the sample had the highest levels of ethanol and acetaldehyde, with concentrations up to 2.6 ppm and 92 ppb, respectively, possibly due to the preparation of dough and baking activities. Indoor‐to‐outdoor concentration ratios indicated that indoor sources were the main contributors to indoor VOC concentrations for the majority of compounds. There was no strong correlation between ventilation and VOC concentrations across all stores. However, increasing the air exchange rates at two stores led to lower indoor VOC concentrations, suggesting that ventilation can be used to reduce concentrations for some specific stores.     

Studying the indoor air quality in three non-residential environments of different use: A museum,a printery industry and an office

The aim of the present study was to identify the main sources contributing to the air pollution of three indoor environments of different use: a museum, a printery industry and an office. For that purpose, particulate matter (TSP, PM₁₀, PM_2.5), inorganic pollutants (NO_x, SO₂, O₃) and organic compounds (BTX, formaldehyde) were monitored. Factors such as the kind of the activities occurred indoors, the emissions from the existing equipment, the number of occupants, the ventilation pattern and the outdoor background substantially varied among the three sites.     

Hazard assessment of chemical air contaminants measured in residences

Identifying air pollutants that pose a potential hazard indoors can facilitate exposure mitigation. In this study, we compiled summary results from 77 published studies reporting measurements of chemical pollutants in residences in the United States and in countries with similar lifestyles. These data were used to calculate representative mid-range and upper-bound concentrations relevant to chronic exposures for 267 pollutants and representative peak concentrations relevant to acute exposures for five activity-associated pollutants. Representative concentrations are compared to available chronic and acute health standards for 97 pollutants. Fifteen pollutants appear to exceed chronic health standards in a large fraction of homes. Nine other pollutants are identified as potential chronic health hazards in a substantial minority of homes, and an additional nine are identified as potential hazards in a very small percentage of homes. Nine pollutants are identified as priority hazards based on the robustness of measured concentration data and the fraction of residences that appear to be impacted: acetaldehyde; acrolein; benzene; 1,3-butadiene; 1,4-dichlorobenzene; formaldehyde; naphthalene; nitrogen dioxide; and PM(2.5). Activity-based emissions are shown to pose potential acute health hazards for PM(2.5), formaldehyde, CO, chloroform, and NO(2). PRACTICAL IMPLICATIONS: This analysis identifies key chemical contaminants of concern in residential indoor air using a comprehensive and consistent hazard-evaluation protocol. The identification of a succinct group of chemical hazards in indoor air will allow for successful risk ranking and mitigation prioritization for the indoor residential environment. This work also indicates some common household activities that may lead to the acute levels of pollutant exposure and identifies hazardous chemicals for priority removal from consumer products and home furnishings.     

室内颗粒污染的源辨识与源解析

辨识室内颗粒物来源与分析室内颗粒物元素特征称为源辨识与源解析,是进行室内空气污染控制与净化的理论依据与前提条件。本文通过对室内空气品质（IAQ）模型进行理论分析,阐明了室内外污染源与室内颗粒物浓度之间的关系。指出室内颗粒污染物研究应根据污染源已知与未知两种情况进行讨论,并针对不同的情况分别采用源辨识与源解析技术。     

Ozone in indoor environments: concentration and chemistry

The concentration of indoor ozone depends on a number of factors, including the outdoor ozone concentration, air exchange rates, indoor emission rates, surface removal rates, and reactions between ozone and other chemicals in the air. Outdoor ozone concentrations often display strong diurnal variations, and this adds a dynamic excitation to the transport and chemical mechanisms at play. Hence, indoor ozone concentrations can vary significantly from hour-to-hour, day-to-day, and season-to-season, as well as from room-to-room and structure-to-structure. Under normal conditions, the half-life of ozone indoors is between 7 and 10 min and is determined primarily by surface removal and air exchange. Although reactions between ozone and most other indoor pollutants are thermodynamically favorable, in the majority of cases they are quite slow. Rate constants for reactions of ozone with the more commonly identified indoor pollutants are summarized in this article. They show that only a small fraction of the reactions occur at a rate fast enough to compete with air exchange, assuming typical indoor ozone concentrations. In the case of organic compounds, the "fast" reactions involve compounds with unsaturated carbon-carbon bonds. Although such compounds typically comprise less than 10% of indoor pollutants, their reactions with ozone have the potential to be quite significant as sources of indoor free radicals and multifunctional (-C=O, -COOH, -OH) stable compounds that are often quite odorous. The stable compounds are present as both gas phase and condensed phase species, with the latter contributing to the overall concentration of indoor submicron particles. Indeed, ozone/alkene reactions provide a link between outdoor ozone, outdoor particles and indoor particles. Indoor ozone and the products derived from reactions initiated by indoor ozone are potentially damaging to both human health and materials; more detailed explication of these impacts is an area of active investigation.     

Indoor and outdoor carbonyl compounds and BTEX in the hospitals of Guangzhou, China

Indoor and outdoor concentration levels of 21 carbonyl compounds and five BTEX (benzene, toluene, ethylbenzene and xylenes) were measured in four hospitals of Guangzhou from 2nd January to 20th March 2004. Samples were collected in five consecutive daytimes for each hospital. Among most of the samples, acetone was the most abundant carbonyl, followed by acetaldehyde, 2-butanone or formaldehyde. Toluene was the most abundant BTEX and the others were at similar levels. The relatively higher acetone concentrations might have resulted from the high level of background in Guangzhou area due to emission of the factories and LPG-fuel vehicles, and also for the special weather conditions during sampling time. The high concentration of acetaldehyde, which was even higher than that of formaldehyde, might be resulted from the wide use of ethanol in hospital. The partial oxidation of ethanol may form acetaldehyde. The indoor concentrations of carbonyls and BTEX were found a little higher than their outdoor counterparts with only a few exceptions, which showed the anthropogenic sources for these compounds. The low correlations between most carbonyls and BTEX concentrations might be caused by their complex sources. Finally, the human exposure levels of formaldehyde and acetaldehyde in hospitals are discussed.     

How do the indoor size distributions of airborne submicron and ultrafine particles in the absence of significant indoor sources depend on outdoor distributions?

Although almost all epidemiological studies of smaller airborne particles only consider outdoor concentrations, people in Central Europe actually spend most of their time indoors. Yet indoor pollutants such as organic gases, allergens and dust are known to play a prominent role, often affecting human health more than outdoor ones. The aim of this study was to ascertain how the indoor particle size distributions of submicron and ultrafine particles correlate with the outdoor concentrations in the absence of significant indoor sources. A typical indoor particle size distribution pattern has one or two modes. In the absence of significant indoor activities such as smoking, cooking etc., outdoor particles were found to be a very important source of indoor particles. The study shows that in the absence of significant indoor sources, the number of indoor concentrations of particles in this size range are clearly lower than the outdoor concentrations. This difference is greater, the higher the number of outdoor concentrations. However, the drop in concentration is not uniform, with the decrease in concentration of smaller particles exceeding that of larger ones. By contrast, the findings with larger particle sizes (diameter > 1 microm) exhibit rather linear concentration decreases. The non-uniform drop in the number of concentrations from outdoors to indoors in our measurements considering smaller particles ( >0.01 microm) is accompanied by a shift of the concentration maxima to larger particle diameters.     

Filtration effectiveness of HVAC systems at near‐roadway schools

Concern for the exposure of children attending schools located near busy roadways to toxic, traffic‐related air pollutants has raised questions regarding the environmental benefits of advanced heating, ventilation, and air‐conditioning (HVAC) filtration systems for near‐road pollution. Levels of black carbon and gaseous pollutants were measured at three indoor classroom sites and at seven outdoor monitoring sites at Las Vegas schools. Initial HVAC filtration systems effected a 31–66% reduction in black carbon particle concentrations inside three schools compared with ambient air concentrations. After improved filtration systems were installed, black carbon particle concentrations were reduced by 74–97% inside three classrooms relative to ambient air concentrations. Average black carbon particle concentrations inside the schools with improved filtration systems were lower than typical ambient Las Vegas concentrations by 49–96%. Gaseous pollutants were higher indoors than outdoors. The higher indoor concentrations most likely originated at least partially from indoor sources, which were not targeted as part of this intervention.     

Penetration of nitrogen oxides and particles from outdoor into indoor air and removal of the pollutants through filtration of incoming air

We studied the effect of ventilation and air filtration systems on indoor air quality in a children's day-care center in Finland. Ambient air nitrogen oxides (NO, NO2) and particles (TSP, PM10) were simultaneously measured outdoors and indoors with automatic nitrogen oxide analyzers and dust monitoring. Without filtration nitrogen oxides and particulate matter generated by nearby motor traffic penetrated readily indoors. With chemical filtration 50-70% of nitrogen oxides could be removed. Mechanical ventilation and filtration also reduced indoor particle levels. During holidays and weekends when there was no opening of doors and windows and no particle-generating activity indoors, the indoor particle level was reduced to less than 10% of the outdoor level. At times when outdoor particle concentrations were high during weekdays, the indoor level was about 25% of the outdoor level. Thus, the possible adverse health effects of nitrogen oxides and particles indoors could be countered by efficient filtration. We also showed that inclusion of heat recovery equipment can make new ventilation installations economical.     

Polycyclic aromatic hydrocarbons: levels and phase distributions in preschool microenvironment

This work aims to characterize levels and phase distribution of polycyclic aromatic hydrocarbons (PAHs) in indoor air of preschool environment and to assess the impact of outdoor PAH emissions to indoor environment. Gaseous and particulate (PM₁ and PM_2.5) PAHs (16 USEPA priority pollutants, plus dibenzo[a,l]pyrene, and benzo[j]fluoranthene) were concurrently sampled indoors and outdoors in one urban preschool located in north of Portugal for 35 days. The total concentration of 18 PAHs (ΣPAHs) in indoor air ranged from 19.5 to 82.0 ng/m³; gaseous compounds (range of 14.1–66.1 ng/m³) accounted for 85% ΣPAHs. Particulate PAHs (range 0.7–15.9 ng/m³) were predominantly associated with PM₁ (76% particulate ΣPAHs) with 5‐ring PAHs being the most abundant. Mean indoor/outdoor ratios (I/O) of individual PAHs indicated that outdoor emissions significantly contributed to PAH indoors; emissions from motor vehicles and fuel burning were the major sources.     

Ozone in Residential Air: Concentrations,I/O Ratios,Indoor Chemistry,and Exposures

Ozone concentrations were measured in indoor and outdoor residential air during the summer of 1992. Six homes located in a New Jersey suburban area were chosen for analysis, and each home was monitored for 6 days under different ventilation and indoor combustion conditions. The 5-hour average ozone concentration outdoors over the monitoring period was 95 ± 36 ppbv. One third of the days exceeded the National Ambient Air Quality Standard (NAAQS), one-hour maximum concentration of 120 ppb. The mean indoor to outdoor (I/O) ratios of ozone concentration ranged from 0.22 ± 0.09 to 0.62 ± 0.11, depending upon ventilation rate and indoor gas combustion. The presence of indoor gas combustion can significantly decrease the I/O ratio. Because of the great amount of time that people spend indoors, the indoor residential exposures were estimated to account for 57% of the total residential exposures. One type of the possible gas-phase reactions for indoor ozone, the reaction of ozone with a volatile organic compound containing unsaturated carbon-carbon bonds, is discussed with some supporting evidence provided in the study.     

Indoor and outdoor BTX levels in German cities

On the basis of the ongoing study INGA (INdoor exposure and Genetics in Asthma), Germany's most detailed and standardized epidemiological study on indoor exposure to both allergens in house dust and volatile compounds in the air of the home environment has been performed. The purpose of this paper is to describe the spatial and seasonal variability of indoor and outdoor BTX (Benzene, toluene, ethyl benzene, ortho-xylene, meta- and para-xylene) concentrations for the study period from June 1995 to November 1996. Within this framework, air concentrations of volatile organic compounds (BTX) were measured in 204 households in Erfurt (Eastern Germany) and 201 households in Hamburg (Western Germany). BTX sampling was conducted over one week using OVM 3500 passive diffusion sampling devices in the indoor (living room and bedroom) and outdoor environment (outside the window of the living room). Indoor and outdoor median BTX concentrations in Erfurt were slightly, but significantly higher than those in Hamburg. This gap was most pronounced in the levels of indoor toluene (37.3 microg/m3 for Erfurt and 20.5 microg/m3 for Hamburg, P < 0.0001). In both cities, winter indoor and outdoor concentrations for the five compounds exceeded the summer values. Outdoor concentrations of ethyl benzene and ortho-xylene were very low (50% < L.D.). In general, the indoor BTX air concentrations were significantly higher than the outdoor concentra- tions, the lowest I/O ratios were found in the case of benzene. Living room and bedroom values for the five compounds were highly correlated (Spearman coefficient 0.5-0.9). Despite the better insulation of the homes in West Germany, no indication for the expected higher indoor concentrations of BTX in the West could be found. The strong and yet undiscovered indoor source for toluene in East Germany might lead to a further increase in the indoor air load in those homes in the East, which undergo renovations which will lead to improved insulation.