Variation in indoor air pollutant concentrations with time in a newly constructed private house

An indoor air quality research project was conducted in a new private house built in January 1997 to investigate time course changes in formaldehyde concentrations during an 11-month period from April 1997 to February 1998. Indoor and outdoor concentrations of volatile organic compounds (VOCs) and nitrogen dioxide were also measured in August 1997 and February 1998. Indoor formaldehyde concentrations were measured 14 times (48 hrs sampling for each measurement) for 28 days in the living room, a bedroom and the kitchen in April '97. The concentrations exceeded the Japanese Government's guideline value of 0.08 ppm in 34 of the 42 (81.0%). Day to day variation in the formaldehyde concentration was found to be substantial, the range being between 0.073 and 0.232 ppm for the bedroom, for example. In June and August '97, values for 20 of 21 measurements exceeded the guideline, the results suggesting that indoor formaldehyde concentrations remain high until 7 months after the completion of construction. There were positive correlations between the formaldehyde concentrations in the living room and the kitchen and personal exposure levels to formaldehyde, the result indicating a direct influence of the home environment. The formaldehyde concentration in the living room also exhibited a positive correlation with the room temperature. Natural ventilation by opening windows was found to be effective for decreasing the concentration of formaldehyde in the indoor air. Indoor VOC concentrations decreased rapidly after the completion of construction except for that of toluene, which was higher than the outdoor concentration even after 7 months. Indoor concentrations of all of the VOCs were, however, found to be almost the same as those outdoor at the 13 month time point. Indoor nitrogen dioxide concentrations measured in the bedroom in winter (February '98) exceeded the Environmental Air Quality Standard in Japan, this result being considered due to use of an oil fan heater. These data suggest that personal exposure levels to formaldehyde and nitrogen dioxide are high in newly constructed private homes in Japan. In order to avoid prolonged exposure to high concentrations of indoor air pollutants, it is considered very important to take measures such as of use building materials with low formaldehyde emissions and to discontinue the use of oil fan heaters.     

Comparisons of seasonal fungal prevalence in indoor and outdoor air and in house dusts of dwellings in one Northeast American county

Fungi cause allergies and many other adverse health effects. In this study, we characterized the nature and seasonal variation of fungi inside and outside homes in the Greater New Haven, Connecticut area. Three indoor air samples (in the living room, bedroom, and basement) and one outdoor sample were collected by the Burkard portable air sampler. House dust samples were collected in the living room by a vacuum cleaner. The mold concentrations varied widely from house to house in both indoor and outdoor air. No significant difference (p>0.05) in concentration and type of fungi between living room and bedroom or by season was observed. Both concentration and type of fungi were significantly higher (p<0.05) in the basement than other indoor areas and outdoor air in winter. The type of fungi in living room, bedroom, and outdoor air were found to have significant changes among seasons, but there was no significant difference for the basement among seasons. Cladosporium spp. was dominant in both indoor and outdoor air in summer. Penicillium and Aspergillus were dominant in indoor air in winter, but neither was dominant in any season in outdoor air. The type of fungi and their concentrations in house dust samples were not representative of those isolated in indoor air. In dust samples, more Mucor, Wallemia, and Alternaria species, but less Aspergillus, Cladosporium, and Penicillium species were found in all seasons. Air sampling in spring or fall in every suspected house is suggested for year-round fungal exposure assessment.     

Comparison of outdoor and indoor mobile source-related volatile organic compounds between low- and high-floor apartments

The current study examined the hypothesis that there may be vertical variation in mobile source-related volatile organic compound (VOC) concentrations in high-rise apartment buildings. One hundred twelve homes in 56 high-rise apartment buildings with 10 or more stories participated in the study. Both the outdoor and the indoor air concentrations of three VOCs [methyl-tertiary butyl ether (MTBE), benzene, and toluene] were significantly higher for the low-floor apartments than for the high-floor apartments (P < 0.05). The median outdoor concentrations were 5.4, 6.8, and 29.1 microgram/m3, respectively, for the low-floor apartments, yet 4.4, 4.3, and 21.9 microgram/m3, respectively, for the high-floor apartments. Meanwhile, the median indoor concentrations were 6.3, 9.4, and 44.8 microgram/m3, respectively, for the low-floor apartments, yet 5.1, 7.6, and 38.8 microgram/m3, respectively, for the high-floor apartments. These findings indicate that residents of low-floor apartments are exposed to elevated residential levels of mobile source-related VOCs compared to high-floor apartment residents. The indoor concentrations of the target VOCs, except for MTBE, were significantly higher than the outdoor air concentrations for both the low and high floors (P < 0.05). Plus, the outdoor and indoor VOC concentrations were significantly different between the daytime and nighttime data sets for both low- and high-floor apartments, with a P value of less than or close to 0.05.     

大连冬季居室主要挥发有机物及二氧化氮检测

目的 了解冬季居室空气中主要挥发性有机物(VOCs)和二氧化氮的污染水平及其影响因素.方法 于2009年1月对辽宁省大连市某小区随机选择装修后不同时期的99户居室,测定卧室、厨房及室外空气中主要挥发性有机物和二氧化氮浓度,同时对居民基本情况进行问卷调查.结果 卧室空气中甲醛、苯、甲苯和二甲苯的浓度分别为37.3,6.8,15.5和9.0μg/m3,厨房分别为39.8,12.7,18.8和9.8μg/m3,卧室和厨房空气中甲醛、苯、甲苯和二甲苯的浓度均高于室外浓度(P＜0.05);装修时间在1年内的卧室和厨房空气中3种苯类有机化合物的浓度均明显高于装修时间≥1年的卧室和厨房空气浓度;摆放绿色植物的居室中甲醛和二氧化氮浓度明显低于未摆放绿色植物的居室(P＜0.05).结论 冬季装修居室内存在主要VOCs污染,其浓度随装修后时间的增加而降低,尤其3种苯类有机化合物的浓度下降较快.室内绿色植物对室内污染物有一定的吸附和消除作用.     

广州市室内环境中苯和甲醛的健康风险评价

目的了解广州市室内环境中苯和甲醛的人群致癌风险。方法2011年7-10月对广州市120个监测点的卧室、客厅、办公室及室外环境中的苯和甲醛浓度进行监测,应用健康风险评价的方法对苯和甲醛的人群致癌风险进行评价。结果卧室空气中的甲醛浓度超过了《室内空气质量标准》（GB／T18883—2002）的限值要求,其他环境中的苯和甲醛浓度低于标准限值。成年男性和成年女性的苯致癌风险值分别为1．39×10-4和1．41×10-4。甲醛的致癌风险值分别为7．81×10-4和7．82×10-4。甲醛的致癌风险高于苯的致癌风险,女性的致癌风险略高于男性,不同人群在不同环境中的苯和甲醛致癌风险值均超过美国环境保护局制定的安全限值（1．00×10-4）。结论广州市室内环境中苯和甲醛对人群存在较大的致癌风险。     

Evaporative gasoline emissions and asthma symptoms

Attached garages are known to be associated with indoor air volatile organic compounds (VOCs). This study looked at indoor exposure to VOCs presumably from evaporative emissions of gasoline. Alaskan gasoline contains 5% benzene making benzene a marker for gasoline exposure. A survey of randomly chosen houses with attached garages was done in Anchorage Alaska to determine the exposure and assess respiratory health. Householders were asked to complete a health survey for each person and a household survey. They monitored indoor air in their primary living space for benzene, toluene, ethylbenzene and xylenes for one week using passive organic vapor monitoring badges. Benzene levels in homes ranged from undetectable to 58 parts per billion. The median benzene level in 509 homes tested was 2.96 ppb. Elevated benzene levels in the home were strongly associated with small engines and gasoline stored in the garage. High concentrations of benzene in gasoline increase indoor air levels of benzene in residences with attached garages exposing people to benzene at levels above ATSDR's minimal risk level. Residents reported more severe symptoms of asthma in the homes with high gasoline exposure (16%) where benzene levels exceeded the 9 ppb.     

Ambient, indoor and personal exposure relationships of volatile organic compounds in Mexico City Metropolitan Area

Air pollution standards and control strategies are based on ambient measurements. For many outdoor air pollutants, individuals are closer to their sources (especially traffic) and there are important indoor sources influencing the relationship between ambient and personal exposures. This paper examines the relationship between volatile organic compounds (VOCs) measured at central site monitoring stations and personal exposures in the Mexico City Metropolitan Area. Over a 1-year period, personal exposures to 34 VOCs were measured for 90 volunteers from 30 families living close to one of five central monitoring stations. Simultaneous 24-h indoor, outdoor and central site measurements were also taken. Dual packed thermal desorption tubes and C(18) DNPH-coated cartridges were used for sampling VOCs and these were analyzed by GC/MS and HPLC, respectively. A factor analysis of the personal exposure data aided in grouping compounds by the most likely source type: vehicular (BTEX, styrene and 1,3-butadiene), secondary formed or photochemical (most aldehydes), building materials and consumer products (formaldehyde and benzaldehyde), cleaning solvents (tetrachloroethene and 1,1,1-trichloroethane), volatilization from water (chloroform and trichloroethene) and deodorizers (1,4-dichlorobenzene). Mean ambient, indoor and personal concentrations were 7/7/14 microg/m(3) for benzene, 1/3/3 for 1,3-butadiene, 6/20/20 for formaldehyde and 3/9/50 for 1,4-dichlorobenzene. Geometric mean (GM) ambient concentrations of trichloroethene and carbon tetrachloride were similar to GM personal exposures. While outdoor and indoor home GM concentrations for most vehicular related compounds (benzene, MTBE, xylenes and styrene) were comparable, the GM personal exposures were twice as high. Indoor concentrations of 1,3-butadiene, 1,1,1-trichloroethane, tetrachloroethane, chloroform, formaldehyde, valeraldehyde, propionaldehyde and n-butyraldehyde were comparable to personal exposures. For certain compounds, such as chloroform, aldehydes, toluene, 1,3-butadiene and 1,4-dichlorobenzene, GM personal exposures were more than two times greater than GM ambient measurements.     

Unmetabolized VOCs in urine as biomarkers of low level exposure in indoor environments

This study aimed to test the possible use of unmetabolized volatile organic compounds (VOCs) in urine as biomarkers of low-level indoor environmental exposure. Twenty-four subjects in 13 dwellings in a prefecture of Japan participated in this study. Air samples of the breathing zone were collected in the living room and bedroom, along with spot urine samples (before bedtime and first morning voids). Toluene, ethylbenzene, xylene isomers, styrene and p-dichlorobenzene in the air and urine samples were measured by gas chromatography/mass spectrometry. For the 21 subjects without solvent exposure at work, there were significant correlations between the time-weighted average air concentrations in the bedroom and morning urinary concentrations for toluene, o-xylene, total xylene and p-dichlorobenzene (correlation coefficients of 0.54, 0.61, 0.56 and 0.84, respectively). Multiple linear regression analysis showed only air VOCs in the bedroom influenced the morning urinary VOC concentrations. We concluded that unmetabolized VOCs in the urine can provide a reliable biological indicator for air VOC exposures in non-occupational environments.     

Exposure to volatile organic compounds in residences adjacent to dyeing industrial complex

Objectives The present study was designed to evaluate residential exposure to selected volatile organic compounds (VOCs) relative to the proximity of the Daegu dyeing industrial complex (DDIC).Methods A series of surveys was conducted to measure the concentrations of five aromatic VOCs (toluene, benzene, m-xylene, p-xylene, and o-xylene) and methyl tertiary-butyl ether (MTBE) in the industrial outdoor air within the DDIC and in residential outdoor and indoor air based on the relative proximity of the DDIC.Results The geometric mean (GM) toluene value for the outdoor air samples from residential area R1 located near the DDIC (255 g/m³) was about seven-times higher than that from residential area R2 located further away from the DDIC (36.9 g/m³), whereas no significant difference was found in the outdoor air concentrations of the other target compounds between the two residential areas. Moreover, the elevated outdoor toluene levels outweighed the indoor sources with respect to the environmental exposure of residents near the DDIC. However, for the other target VOCs there was no significant difference between the residential exposure of residents living close to and a certain distance away from the DDIC.Conclusions The present study confirmed that residents in neighborhoods near the DDIC were exposed to elevated outdoor toluene levels compared with residents living further away from such a source. Furthermore, it appeared that the DDIC was a potential contributor to the nearby residential outdoor toluene levels.Essential results have not been and will not be published elsewhere     

Personal exposure to volatile organic compounds in the Czech Republic

Personal exposures to volatile organic compounds (VOCs) were measured in the three industrial cities in the Czech Republic, Ostrava, Karvina and Havirov, while the city of Prague served as a control in a large-scale molecular epidemiological study identifying the impacts of air pollution on human health. Office workers from Ostrava and city policemen from Karvina, Havirov and Prague were monitored in the winter and summer of 2009. Only adult non-smokers participated in the study (N=160). Radiello-diffusive passive samplers were used to measure the exposure to benzene, toluene, ethylbenzene, meta- plus para-xylene and ortho-xylene (BTEX). All participants completed a personal questionnaire and a time-location-activity diary (TLAD). The average personal BTEX exposure levels in both seasons were 7.2/34.3/4.4/16.1?μg/m(3), respectively. The benzene levels were highest in winter in Karvina, Ostrava and Prague: 8.5, 7.2 and 5.3?μg/m(3), respectively. The personal exposures to BTEX were higher than the corresponding stationary monitoring levels detected in the individual localities (P<0.001; except m,p-xylene in summer). The indoor environment, ETS (environmental tobacco smoke), cooking, a home-heating fireplace or gas stove, automobile use and being in a restaurant were important predictors for benzene personal exposure. Ostrava's outdoor benzene pollution was a significant factor increasing the exposure of the Ostrava study participants in winter (P<0.05).     

The Los Angeles TEAM Study: personal exposures, indoor-outdoor air concentrations, and breath concentrations of 25 volatile organic compounds.

The U.S. Environmental Protection Agency and the California Air Resources Board studied the exposures of 51 residents of Los Angeles, California, to 25 volatile organic chemicals (VOCs) in air and drinking water in 1987. A major goal of the study was to measure personal, indoor, and outdoor air concentrations, and breath concentrations of VOCs in persons living in households that had previously been measured in 1984. Other goals were to confirm the marked day-night and seasonal differences observed in 1984; to determine room-to-room variability within homes; to determine source emission rates by measuring air exchange rates in each home; and to extend the coverage of chemicals by employing additional sampling and analysis methods. A total of 51 homes were visited in February of 1987, and 43 of these were revisited in July of 1987. The results confirmed previous TEAM Study findings of higher personal and indoor air concentrations than outdoor concentrations of all prevalent chemicals (except carbon tetrachloride); higher personal, indoor, and outdoor air concentrations in winter than in summer; and (in winter only) higher outdoor concentrations at night than in the daytime. New findings included the following: (1) room-to-room variability of 12-hour average concentrations was very small, indicating that a single monitor may be adequate for estimating indoor concentrations over this time span; (2) "whole-house" source emission rates were relatively constant during both seasons, with higher rates for odorous chemicals such as p-dichlorobenzene and limonene (often used in room air fresheners) than for other classes of chemicals; (3) breath concentrations measured during morning and evening were similar for most participants, suggesting the suitability of breath measurements for estimating exposure in the home; (4) limited data obtained on two additional chemicals-toluene and methylene chloride-indicated that both were prevalent at fairly high concentrations and that indoor air concentrations exceeded outdoor concentrations by a factor of about three.     

Levels of volatile organic compounds in homes in Dalian,China

This paper measured selected individual volatile organic compounds (VOCs), including formaldehyde, in residences in Dalian, evaluated the association between the apartment characteristics and VOC concentrations, and explored the associations between chemicals and sick building syndrome (SBS). Higher VOC concentrations were measured indoors than outdoors in summer (August to September) and winter (January to March) in Dalian, and there were no strong correlations between the indoor and outdoor concentrations of most VOCs. This indicates the dominance of indoor sources as compared to outdoor sources. Formaldehyde was the most abundant compound in this study, followed by toluene, benzene, xylene, and styrene. These pollutants increase the occurrence of SBS. Thus, the VOC levels in dwellings in Dalian should be regulated, in view of SBS risks.     

Personal, indoor, and outdoor VOC exposures in a probability sample of children

As part of the Minnesota Children's Pesticide Exposure Study we measured volatile organic compound (VOC) concentrations in a probability sample of households with children. The 6-day average concentrations for 10 common VOCs were obtained in urban and nonurban residences twice during this multiphase study: screening-phase indoor measurements were collected in 284 households, and in the intensive-phase matched outdoor (O), indoor (I), and personal (P) measurements were collected in a subset (N=72) of the screened households. Screening-phase households with smokers had significantly higher concentrations of benzene and styrene compared to nonsmoking households; households with an attached garage had significantly higher levels of benzene, chloroform, styrene, and m/p- and o-xylene compared to households without an attached garage; and nonurban residences, which had a greater prevalence of smokers and attached garages, had significantly higher 1,1,1-trichloroethane, styrene, and toluene and significantly lower tetrachloroethylene concentrations compared to urban households. The screening-phase weighted distributions estimate the mean and variability in indoor VOC concentrations for more than 45,000 households with children in the census tracts sampled. Overall, median indoor concentrations of most VOCs measured in this study were similar to or lower than indoor levels measured previously in the United States. Intensive-phase outdoor VOC concentrations were generally lower than other major metropolitan areas, but urban concentrations were significantly higher than nonurban concentrations for all compounds except 1,1,1-trichloroethylene. A consistent pattern of P>I>O was observed for nine of 10 VOCs, with 1,1,1-trichloroethylene (I>P>O) being the only exception to this pattern. For most children, the indoor at-home microevironment was strongly associated with personal exposure after controlling for important covariates, but the ratio of median to upper bound exposures was smaller than that observed in studies of adults. There are relatively little data on VOC exposures in children, so these results are useful for estimating the central tendency and distribution of VOC exposures in locations where children spend a majority of their time.     

某部新装修居室空气质量调查分析

目的了解新装修居室室内空气质量情况,探讨室内污染物种类及其污染途径。方法检测对象为某区申请空气质量检测的28户新装修2个月后住宅。采用4160型甲醛分析仪测定甲醛浓度,以甲醛浓度高于0.08 mg/m3为超标剂量计算超标率。总挥发性有机化合物(TVOC)的测定采用总挥发性有机化合物PGM-7240/7240K检测仪,以TVOC浓度高于0.5 mg/m3为超标剂量,计算超标率。氡的测定采用1027型测氡仪,以浓度高于100 Bq/m3为超标剂量,计算超标率。结果室内居室甲醛浓度全部超过国家标准,厨房、主卧,主卫,客卧浓度高于卫生间和客厅;主卫、书房、主卧超标率显著高于客厅,具有统计学意义。厨柜内甲醛浓度显著高于室内空气甲醛浓度(P<0.05)。除卫生间外,室内不同居室TVOC浓度全部超过国家标准,厨房、主卧TVOC浓度高于卫生间;书房、客卧TVOC超标率显著高于卫生间超标率。各居室氡浓度均在国家标准范围内。结论新装修居室经过2个月时间后,室内甲醛、TVOC浓度仍较高,多数超过国家标准,氡多数在国家标准范围内。     

哈尔滨市女性肺癌危险因素分析—室内空气污染

An investigation including a matched case-control study and measurement of indoor air pollution, of risk factors for female lung adenocarcinoma in Haerbin showed that high coal consumption index (HCCI OR = 10.59), indoor smog pollution in winter (OR = 15.19) and low ceiling height of the living room (OR = 12.49) were main risk factors for the cancer. It was further confirmed by the measurement that the mean daily measured concentrations of TSP and Bap in inhabitants' bedroom in winter were 4.4 and 26.7 times respectively as high as those of outdoor air concentrations. No significant association with cigarette smoking and indoor passive smoking was found.     

Relationships between levels of volatile organic compounds in air and blood from the general population

The relationships between levels of volatile organic compounds (VOCs) in blood and air have not been well characterized in the general population where exposure concentrations are generally at parts per billion levels. This study investigates relationships between the levels of nine VOCs, namely, benzene, chloroform, 1,4-dichlorobenzene, ethylbenzene, methyl tert-butyl ether (MTBE), tetrachloroethene, toluene, and m-/p- and o-xylene, in blood and air from a stratified random sample of the general US population. We used data collected from 354 participants, including 89 smokers and 265 nonsmokers, aged 20-59 years, who provided samples of blood and air in the National Health and Nutrition Examination Survey (NHANES) 1999-2000. Demographic and physiological characteristics were obtained from self-reported information; smoking status was determined from levels of serum cotinine. Multiple linear regression models were used to investigate the relationships between VOC levels in air and blood, while adjusting for effects of smoking and demographic factors. Although levels of VOCs in blood were positively correlated with the corresponding air levels, the strength of association (R(2)) varied from 0.02 (ethylbenzene) to 0.68 (1,4-DCB). Also the blood-air relationships of benzene, toluene, ethylbenzene, and the xylenes (BTEX) were influenced by smoking, exposure-smoking interactions, and by gender, age, and BMI, whereas those of the other VOCs were not. Interestingly, the particular exposure-smoking interaction for benzene was different from those for toluene, ethylbenzene, and the xylenes. Whereas smokers retained more benzene in their blood at increasing exposure levels, they retained less toluene, ethylbenzene, and xylenes at increasing exposure levels. Investigators should consider interaction effects of exposure levels and smoking when exploring the blood-air relationships of the BTEX compounds in the general population.     

Ambient levels of volatile organic compounds in the vicinity of petrochemical industrial area of Yokohama,Japan

Urban ambient air concentrations of 39 aromatic (including benzene, toluene, and xylenes) and aliphatic volatile organic compounds (VOCs) were measured in Yokohama city, Japan. Yokohama city was selected as a case study to assess the amount of VOC released from Industrial area to characterize the ambient air quality with respect to VOC as well as to know the impact of petrochemical storage facilities on local air quality. For this purpose, ambient air samples were collected (from June 2007 to November 2008) at six selected locations which are designated as industrial, residential, or commercial areas. To find out the diurnal variations of VOC, hourly nighttime sampling was carried out for three nights at one of the industrial locations (Shiohama). Samples were analyzed using gas chromatographic system (GC-FID). Results show strong variation between day and nighttime concentrations and among the seasons. Aliphatic fractions were most abundant, suggesting petrochemical storage facilities as the major source of atmospheric hydrocarbons. High concentrations of benzene, toluene, ethyl benzene, and xylene (BTEX) were observed at industrial locations. BTEX showed strong diurnal variation which is attributed to change in meteorology. During our campaign, low ambient VOC concentrations were observed at the residential site.     

The influence of personal activities on exposure to volatile organic compounds

Seven persons volunteered to perform 25 common activities thought to increase personal exposure to volatile organic chemicals (VOCs) during a 3-day monitoring period. Personal, indoor, and outdoor air samples were collected on Tenax cartridges three times per day (evening, overnight, and daytime) and analyzed by GC-MS for 17 target VOCs. Samples of exhaled breath were also collected before and after each monitoring period. About 20 activities resulted in increasing exposure to one or more of the target VOCs, often by factors of 10, sometimes by factors of 100, compared to exposures during the sleep period. These concentrations were far above the highest observed outdoor concentrations during the length of the study. Breath levels were often significantly correlated with previous personal exposures. Major exposures were associated with use of deodorizers (p-dichlorobenzene); washing clothes and dishes (chloroform); visiting a dry cleaners (1,1,1-trichloroethane, tetrachloroethylene); smoking (benzene, styrene); cleaning a car engine (xylenes, ethylbenzene, tetrachloroethylene); painting and using paint remover (n-decane, n-undecane); and working in a scientific laboratory (many VOCs). Continuously elevated indoor air levels of p-dichlorobenzene, trichloroethylene, 1,1,1-trichloroethane, carbon tetrachloride, decane, and undecane were noted in several homes and attributed to unknown indoor sources. Measurements of exhaled breath suggested biological residence times in tissue of 12-18 hr and 20-30 hr for 1,1,1-trichloroethane and p-dichlorobenzene, respectively.     

Exposure to hazardous air pollutants in underground car parks in Guangzhou,China

Volatile organic compounds (VOCs), carbon monoxide (CO), and PM₁₀ were studied by field sampling in six underground car parks beneath multi-level buildings in Guangzhou, China. CO and PM₁₀ in the car parks range from 3.0 to 69.0 ppm and 0.087 to 0.698 mg m^?3, with mean concentrations of 10.8 ppm and 0.228 mg m^?3, respectively. Overall mean concentrations of methyl tertiary-butyl ether (MTBE), benzene, toluene, ethyl-benzene, and xylene (BTEX) are 90.5, 54.8, 239.9, 47.7, and 189.3 μg m^?3, respectively. Indoor air pollutants in the car parks show an obvious seasonal variation and are higher in winter than in summer. The total estimated cancer risks of occupational exposure for car park staff and casual exposure for parking users are 3.73 × 10^?4 and 5.60 × 10^?6, indicating definite and possible risks, respectively. The hazard quotient of target VOCs is 4.33, implying a definite risk for people using underground car parks. Indoor/outdoor (I/O) ratios for MTBE and BTEX are significantly higher than one, reflecting strong emission sources in underground car parks. The BTEX to MTBE ratios in the car parks are almost the same as those in tunnel air, indicating that indoor aromatic hydrocarbons were mainly from engine emissions and gasoline evaporation. With increasing urbanization in China, more attention should be paid to the exposure of staff and users to hazardous air pollutants in underground car parks.     

Exposure to air pollutants in English homes

BRE has conducted a national representative survey of air pollutants in 876 homes in England, designed to increase knowledge of baseline pollutant levels and factors associated with high concentrations. Homes were monitored for carbon monoxide (CO), nitrogen dioxide (NO(2)), formaldehyde and volatile organic compounds (VOCs). In the majority of the homes, concentrations of the measured pollutants were low. However, some homes have concentrations that would suggest a need for precautionary mitigation. Those factors that are most likely to lead to exposures of concern in homes are identified as gas cooking (for CO and NO(2)), the use of unflued appliances for heating (for CO and NO(2)), emissions from materials in new homes (for total VOC (TVOC) and formaldehyde), and painting and decorating, with a significant increase in risk suspected to exist where there is not a place to store materials away from the living space (for TVOC). It is noteworthy that seasonal effects on CO and NO(2) were largely due to indoor sources. This would need to be considered when interpreting time series studies of the effect of outdoor air pollution on health. It is also of some significance that the critical factors are related much more to sources than to ventilation: source control is therefore, as would be expected, the most appropriate approach to reducing the risk of hazardous exposure to air pollutants in homes.