Volatile Organic Compounds in Ventilating Air in Buildings at Different Sampling Points in the Buildings and their Relationship with the Prevalence of Occupant Symptoms

Total volatile organic compounds (TVOC) are determined in intake, room-supply and room air in 86 office rooms in 29 office buildings in northern Sweden. Measurements of formaldehyde were also made in room air. Building and room characteristics were identified and symptom reports collected from 1087 office workers. Concentrations of TVOC and formaldehyde in room air were low, with mean values of 71 µg/m³ and 31 µg/m³, respectively. The TVOC concentration was generally lower in room air than in supply air or intake air. The “loss” (difference in measured values) of TVOC from supply to room air was associated with raised concentrations of formaldehyde and raised prevalences of occupant symptoms. High TVOC concentrations in room air were associated with reduced prevalences of occupant symptoms.     

Concentrations of Volatile Organic Compounds in Indoor Air – A Review

A review is presented of investigations of volatile organic compound (VOC) concentrations in indoor air of buildings of different classifications (dwellings, offices, schools, hospitals) and categories (established, new and complaint buildings). Measured concentrations obtained from the published literature and from research in progress overseas were pooled so that VOC concentration profiles could be derived for each building classification/category. Mean concentrations of individual compounds in established buildings were found to be generally below 50 μg/m³, with most below 5 μg/m³. Concentrations in new buildings were much greater, often by an order of magnitude or more, and appeared to arise from construction materials and building contents. The nature of these sources and approaches to reduce indoor air concentrations by limiting source VOC emissions is discussed. Total VOC (TVOC) concentrations were substantially higher than concentrations of any individual VOCs in all situations, reflecting the large number of compounds present, but interpretation of such measurements was limited by the lack of a common definition for TVOC relevant to occupant exposure.     

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.     

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.     

Personal exposures to volatile organic compounds among outdoor and indoor workers in two Mexican cities

There are limited data on exposures to ambient air toxics experienced by inhabitants of urban areas in developing countries that have high levels of outdoor air pollution. In particular, little is known about exposures experienced by individuals working outdoors - typically as part of the informal sector of the economy - as compared to workers in office-type environments that approach the indoor air quality conditions of the more developed countries. The objective of this study is to explore these differences in personal exposures using a convenience sample of 68 outdoor and indoor workers living in Mexico City (higher outdoor air pollution) and Puebla (lower outdoor air pollution), Mexico. Occupational and non-occupational exposures to airborne volatile organic compounds (VOCs) were monitored during a 2 day period, monitoring 2 consecutives occupational and non-occupational periods, using organic vapor monitors (OVMs). Socio-demographic and personal time-location-activity information were collected by means of questionnaires and activity logs. Outdoor workers experienced significantly higher exposures to most VOCs compared to indoor workers in each of these cities. The outdoor workers in Mexico City had the highest exposures both during- and off-work, with maximum occupational exposures for toluene, MTBE, n-pentane, and d-limonene exceeding 1 mg/m(3). The inter-city pattern of exposures between the outdoor workers is consistent with the higher outdoor air pollution levels in Mexico City, and is above exposures reported for urban areas of the more developed countries. Results from this study suggest that elevated outdoor air pollution concentrations have a larger impact on outdoor workers' personal exposures compared to the contribution from indoor pollution sources. This contrasts with the more dominant role of indoor air VOC contributions to personal exposures typically reported for urban populations of the more developed countries.     

A Review and a Limited Comparison of Methods for Measuring Total Volatile Organic Compounds in Indoor Air

Numerous methods attempt to measure the combined concentrations of volatile organic compounds (VOCs) in indoor air as total VOCs (TVOC). This paper reviews TVOC methods recently presented in the literature and at an international conference on indoor air quality, for the purpose of identifying common practices and of assessing the impacts that choices of sample collection media and analytical methods and instrumentation can have on TVOC results. The paper also presents the results of laboratory and field comparisons of three TVOC methods. These are a flame-ionization-detector (FID) method, a gas chromatography/mass spectrometry (GC/MS) method, and a method employing a photoacoustic infrared (IR) gas monitor. The laboratory experiments were conducted with eight different mixtures of VOCs. The FID method demonstrated an average accuracy of 93 ± 18 percent when the measured values were calculated as concentrations of carbon. The FID and GC/MS methods demonstrated average accuracies of 77±37 and 75±22 percent, respectively, when the measured hydrocarbon-equivalent values were compared to the expected mass concentrations of the mixtures. The higher uncertainty for the FID was largely due to the low mass response of 27 percent for chlorinated compounds. The response of the IR gas monitor varied between 6 and 560 percent for different classes of compounds. Air samples from ten buildings were analyzed by both the FID and GC/MS methods. The results were highly correlated and similar, with the GC/MS values approximately 20 percent higher on average.     

A Pilot Study to Measure Indoor Concentrations and Emission Rates of Polycyclic Aromatic Hydrocarbons

Sampling and analytical methods for gas- and particulate-phase polycylic aromatic hydrocarbons (PAH) in indoor air were evaluated in a controlled field study. Using 12-h, 25-m³ samples, gas-phase PAH were collected on XAD-4 resin and analyzed by GC-MS, and particulate-phase PAH were collected in filters and analyzed for by HPLC with fluorescence detection. Tests were conducted in homes and office buildings without active combustion sources and with gas stoves, wood stoves and cigarette smoking as controlled sources. Indoor concentrations, outdoor concentrations and air-exchange rates were simultaneously measured. The precisions of the concentrations were evaluated using collocated sample pairs collected indoors and outdoors. Net emission rates were calculated for the gas-phase PAH. Net emissions of these compounds were measured in buildings without active combustion sources. Environmental tobacco smoke was identified as a significant source of both gas- and particulate-phase PAH.     

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.     

Outdoor Air Contaminants and Indoor Air Quality under Transient Conditions

The indoor concentrations of contaminants originating from outdoor sources have been measured and calculated under transient conditions. The results show that contaminants that are supplied to an office building via the ventilation system can reach considerably high concentration levels. The indoor/outdoor concentration ratio and time lag are dependent on the air change rate. In buildings with low air change rates the indoor concentration variations are smoothed out compared to buildings with high air change rates. The results from the theoretical model are compared to the results from both laboratory and field measurements and the model is verified for well mixed conditions in a 20 m³ test chamber. The model can be used to simulate different control strategies for reduction of indoor contaminant concentrations related to outdoor sources. One such control strategy is based on reduction of the outdoor air change rate during periods with peak outdoor contaminant concentrations.     

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.     

Functional group characterization of indoor, outdoor, and personal PM: results from RIOPA

Fourier transform infrared (FTIR) spectra of outdoor, indoor, and personal fine particulate matter (PM(2.5)) samples were collected during the Relationship of Indoor, Outdoor, and Personal Air (RIOPA) study. FTIR spectroscopy provides functional group information about the entire PM(2.5) sample without any chemical preparation. It is particularly important to characterizing the poorly understood organic fraction of PM(2.5). To our knowledge this is the first time that FTIR spectroscopy has been applied to a PM(2.5) exposure study. The results were used to chemically characterize indoor air and personal exposure. Sulfate was strongest in outdoor samples, which is consistent with the generally accepted understanding that sulfate is of outdoor origin. Absorbances attributed to soil dust were also seen in many outdoor and some indoor and personal samples. Inorganic nitrate absorbances were a common feature of many California and some New Jersey samples. Carbonyl absorbances showed substantial variation in strength, number of peaks, and wave number shift between samples, indicating variability in composition and sources. Absorbances attributed to aliphatic hydrocarbon and amide functional groups were enhanced in many personal and indoor samples, which suggested the influence of indoor sources in these homes. We speculate that meat cooking is one possible source of particulate amides. PRACTICAL IMPLICATIONS: To our knowledge this is the first time that FTIR spectroscopy has been used to characterize the composition of indoor and personal PM(2.5). The presence of sulfate, nitrate, ammonium, soil dust and a number of organic functional groups are all detected in one analysis on filter samples without extraction or other sample preparation. Differences between indoor and outdoor spectra are used to identify spectral features due to indoor-generated PM(2.5). Particularly interesting are the much larger aliphatic absorbances, shifts in carbonyl absorbances, and occasional small amide absorbances found in indoor and personal spectra but rarely in outdoor spectra. These observations are important because organics make up a large portion of PM(2.5) mass and their composition and properties are poorly characterized. The properties and behavior of organic compounds in airborne particles are often predicted based on their functional group composition. This analysis begins the development of a better understanding of the functional group composition of indoor and personal PM(2.5) and how it differs from that of outdoor PM(2.5). Eventually this will lead to an improved understanding of the properties, behavior and effects of PM(2.5) of indoor and outdoor origin.     

Volatile organic compounds, polycyclic aromatic hydrocarbons and elements in the air of ten urban homes

Ten homes were monitored at regular intervals from June 1994 through April 1995 as part of a Public Health Assessment in Southeast Chicago for exposure to volatile organic compounds (VOCs), polycyclic aromatic hydrocarbons (PAHs), and elements. Simultaneous 24-h indoor and outdoor samples were collected. VOCs were and analyzed using USEPA Method TO-14 with Selected Ion Monitoring Mass Spectrometry (GC/MS). PAHs were analyzed using USEPA Method TO-13 with GC/MS. Elements were collected on quartz fiber filters and analyzed by Inductively Coupled Argon Plasma (ICP) spectroscopy or Graphite Furnace Atomic Absorption (GFAA). Continuous measurements of CO2 and temperature were recorded for each indoor sample. Twenty-four h total CO2 emissions were determined from occupancy and estimated gas stove usage and were moderately correlated (R2 = 0.19) with 24 h average indoor CO2 concentrations. Modeled 24-h air exchange rates ranged from 0.04 to 3.76 air changes h-1 (ACH), with mean of 0.52 ACH. Median particle penetration was 0.89. Emission rates were calculated for each pollutant sampled. Using a detailed housing survey and field sampling questionnaires, it was possible to evaluate associations between housing characteristics and source activities, and pollutant source rates. The data indicate that several predictor variables, including mothball storage, air freshner use, and cooking activities, are reasonable predictors for emission rates for specific pollutants in the homes studied.     

板式儿童家具中挥发性有机物（TVOC）对室内空气质量影响的研究

对北京流通领域的板式儿童家具分别进行抽样,参照国际标准ISO16000-9对其TVOC释放量进行了试验研究。测试结果表明：测量获得挥发性有机化合物种类高达60种,有酸、醛、醇、芳香烃、烷烃等多大类型。4个样品舱内TVOC含量,均未达到室内空气质量标准的TVOC限量要求。儿童家具是形成儿童房室内空气中挥发性有机物的一个主要来源。提出了可行、有效的家具检测测试方案。     

Indoor gaseous air pollutants determinants in office buildings—The OFFICAIR project

The aim of this study was to identify determinants of aldehyde and volatile organic compound (VOC) indoor air concentrations in a sample of more than 140 office rooms, in the framework of the European OFFICAIR research project. A large field campaign was performed, which included (a) the air sampling of aldehydes and VOCs in 37 newly built or recently retrofitted office buildings across 8 European countries in summer and winter and (b) the collection of information on building and offices’ characteristics using checklists. Linear mixed models for repeated measurements were applied to identify the main factors affecting the measured concentrations of selected indoor air pollutants (IAPs). Several associations between aldehydes and VOCs concentrations and buildings’ structural characteristic or occupants’ activity patterns were identified. The aldehyde and VOC determinants in office buildings include building and furnishing materials, indoor climate characteristics (room temperature and relative humidity), the use of consumer products (eg, cleaning and personal care products, office equipment), as well as the presence of outdoor sources in the proximity of the buildings (ie, vehicular traffic). Results also showed that determinants of indoor air concentrations varied considerably among different type of pollutants.     

Monitoring of indoor volatile organic compounds and polycyclic aromatic hydrocarbons arising from kerosene cooking fuel.

Air samples, representing indoor environments of a kitchen in which a kerosene stove was used were collected and analysed for volatile organic compounds (VOCs) viz., n-hexane, benzene, heptane, toluene, p- and o-xylene and n-decane using a cryogenic preconcentration system and a gas chromatograph with a flame-ionisation detector. Simultaneous outdoor samples were also collected to determine indoor to outdoor (I/O) ratios for each compound. Reversed phase high performance liquid chromatography (HPLC) with ultra violet absorption detection was optimised for separation and quantification of polycyclic aromatic hydrocarbons (PAHs) in air particulate matter. Concentration of total suspended particulate matter (TSPM), benzene soluble organics and the PAHs in air samples collected in indoor environment of some tenements at Trombay, Mumbai where kerosene is used as cooking fuel are discussed in relation to the concentration of the same in outdoor environment in vicinity of the tenement. VOCs and PAHs results from samples collected in kitchens in Trombay are discussed in relation to indoor air pollution.     

High temporal variability in airborne bacterial diversity and abundance inside single‐family residences

Our homes are microbial habitats, and although the amounts and types of bacteria in indoor air have been shown to vary substantially across residences, temporal variability within homes has rarely been characterized. Here, we sought to quantify the temporal variability in the amounts and types of airborne bacteria in homes, and what factors drive this variability. We collected filter samples of indoor and outdoor air in 15 homes over 1 year (approximately eight time points per home, two per season), and we used culture‐independent DNA sequencing approaches to characterize bacterial community composition. Significant differences in indoor air community composition were observed both between homes and within each home over time. Indoor and outdoor air community compositions were not significantly correlated, suggesting that indoor and outdoor air communities are decoupled. Indoor air communities from the same home were often just as different at adjacent time points as they were across larger temporal distances, and temporal variation correlated with changes in environmental conditions, including temperature and relative humidity. Although all homes had highly variable indoor air communities, homes with the most temporally variable communities had more stable, lower average microbial loads than homes with less variable communities.     

Indoor exposure levels of ammonia in residences,schools, and offices in China from 1980 to 2019: A systematic review

Indoor ammonia (NH₃) pollution has been paid more and more attention in view of its health risk. However, few studies have investigated the exposure level in the non-occupational environment in China. This study systematically reviewed the indoor ammonia exposure level in different regions, the equivalent exposure concentration of different populations, and the factors that influence indoor air ammonia in residences, offices, and schools in China. The literature published in 1980–2019 from main databases was searched and detailed screened, and finally, 56 related studies were selected. The results illustrated that the median concentration of indoor air ammonia in residences, offices, and school buildings was 0.21 mg/m³, 0.26 mg/m³, and 0.15 mg/m³. There were 46.4%, 71.4%, and 40% of these samples exceeding the NH₃ standard, respectively. The national concentrations and the equivalent exposure levels of adults and children were calculated and found to be higher than 0.20 mg/m³. The concentration of ammonia varied greatly in different climate zones and economic development regions. Higher concentrations were found in the severe cold zone and the regions with higher economic level. This review reveals a high exposure risk of indoor air ammonia and the crucial impact of human emission, indoor air temperature, new concrete, and economic level, suggesting further investigation on indoor air ammonia evaluation and health effects.     

Indoor air quality in the university libraries of Modena (Italy)

We carried out a survey in 16 libraries of the University of Modena, Northern Italy, to assess the indoor exposure to volatile organic compounds (VOCs), including formaldehyde, and total dusts. Data were collected on the main structural characteristics of the buildings; indoor microclimate parameters, such as temperature, relative humidity and ventilation rate were measured and air samples taken inside and outside the libraries. The mean value of total dusts was 190 +/- 130 microg/m3 with a wide range of values. Formaldehyde was found in only ten out of 16 libraries and the indoor concentrations ranged from 1.70 to 67.8 microg/m3 with an average value of 32.7 +/- 23.9 microg/m3. On the whole, VOCs were present in all the libraries investigated with an average value was 433 +/- 267 microg/m3 (range 102-936 microg/m3). No correlation was found among VOCs, formaldehyde and total dusts nor was a significant association observed with microclimatic parameters or the structural characteristics of the buildings. The general situation found in this study suggests no major problems related to indoor pollution. However, some of the pollutants investigated such as total dust and total VOCs deserve further investigation. It is important to identify the possible sources of contaminants and to define the relationship between indoor and outdoor levels of pollutants more accurately, taking into account the effects of air recycling due to natural ventilation systems.     

Total Volatile Organic Compounds (TVOC) in Indoor Air Quality Investigations*

Abstract The amount of volatile organic compounds (VOCs) in indoor air, usually called TVOC (total volatile organic compounds), has been measured using different definitions and techniques which yield different results. This report recommends a definition of TVOC referring to a specified range of VOCs and it proposes a method for the measurement of this TVOC entity. Within the specified range, the measured concentrations of identified VOCs (including 64 target compounds) are summed up, concentrations of non-identified compounds in toluene equivalents are added and, together with the identified VOCs, they give the TVOC value. The report reviews the TVOC concept with respect to its usefulness for exposure assessment and control and for the prediction of health or comfort effects. Although the report concludes that at present it is not possible to use TVOC as an effect predictor, it affirms the usefulness of TVOC for characterizing indoor pollution and for improving source control as required from the points of view of health, comfort, energy efficiency and sustainability.     

装饰材料引起室内VOC污染的防治

论述了室内空气质量的重要性以及室内挥发性有机物（VOC）对健康的危害,介绍了评价VOC污染的量化指标TVOC和减少室内VOC污染的技术和措施。