Comparison of indoor and outdoor air quality at two staff quarters in Hong Kong

The indoor and outdoor air quality of two staff quarters of Hong Kong Polytechnic University at Tsim Sha Tsui East (TSTE) and Shatin (ST) were investigated. The air sampling was carried out in winter for about two months starting from January to February of 1996. Fifteen flats from each staff quarter were randomly selected for indoor/outdoor air pollutant measurements. The pollutants measured were NO_x, NO, NO₂, SO₂, CO, and O₃. The variations of pollutant concentrations between indoor and outdoor air were investigated on weekday mornings, weekday evenings, weekend mornings, and weekend evenings. All indoor/outdoor pollutant concentrations measured did not exceed the ASHRAE/NAAQS standard. The carbon monoxide concentrations indoors were systemically higher than those outdoors at the TSTE and the ST quarters, both on weekdays and Sunday, which indicates there are CO sources indoors. Except for CO, the indoor levels of other pollutants (NO_x, NO, NO₂, SO₂, and O₃) are lower than those outdoors. There was a significant correlation (P < 0.05) between indoor and outdoor concentrations for SO₂ and O₃ at both the TSTE and the ST quarters. Except for O₃, the mean concentrations of all the pollutants in the TSTE quarters, both indoor and outdoor, were higher than that of the ST quarters in all sampling periods. All indoor and outdoor O₃ levels were lower at the TSTE quarters than those at the ST quarters. The O₃ ratios of TSTE/ST were 0.72 outdoor and 0.79 indoor. This can be explained by the NO titration reaction through NO conversion to NO₂.     

The effects of woodburning on the indoor residential air quality

Data from suburban residences in the Boston metropolitan area reveal a potential adverse impact on indoor air quality from woodburning in woodstoves and fireplaces. Ambient pollutant concentrations at each residence were compared to corresponding pollutant levels indoors at three locations (kitchen, bedroom, and activity room). Individual gaseous pollutant samples were averaged on an hourly basis while 24-h integrated samples of particulate matter were obtained. Ten gaseous pollutants were sampled along with total suspended particulates (TSP). Chemical analyses further determined ten components of TSP including trace metals, benzo-a-pyrene(B)aP, respirable suspended particulates (RSP), and water soluble sulfates and nitrates. Monitoring lasted two weeks at each residence and was conducted under occupied, real-life, conditions. Observed, elevated indoor concentrations of TSP, RSP, and BaP are attributed to woodburning. Data indicate that average indoor TSP concentrations during woodburning periods were about three times corresponding levels during nonwoodburning periods. The primary 24-h national ambient air quality standard (NAAQS) for TSP was exceeded once indoors during fireplace use, and the secondary, 24-h TSP NAAQS, was also exceeded indoors by RSP concentrations. Indoor BaP concentrations during woodstove use averaged five times more than during nonwoodburning periods. At this stage, results are only indicative, but the potential impact from elevated indoor concentrations of TSP, RSP, and BaP, attributed to woodburning, may have long-term health implications.     

Comparative overview of indoor air quality in Antwerp, Belgium

This comprehensive study, a first in Belgium, aimed at characterizing the residential and school indoor air quality of subgroups that took part in the European Community Respiratory Health Survey and the International Study of Asthma and Allergy in Childhood [Masoli M, Fabian D, Holt S, Beasley R. Global Burden of Asthma, Medical Research Institute of New Zealand, University of Southampton; 2004.] questionnaire-based asthma and related illnesses studies. The principal aim was to perform a base-line study to assess the indoor air quality in Antwerp in terms of various gaseous and particulate pollutants. Secondly, it aimed to establish correlations between these pollutants investigated, the pollutant levels in the indoor and outdoor micro-environments, findings of the previous questionnaire-based studies and an epidemiological study which ran in conjunction with this study. Lastly, these results were compared and evaluated with current indoor and ambient guidelines in various countries This paper presents selected results on PM1, PM2.5 and PM10 mass concentrations and elemental C estimates as black smoke, as well as gaseous NO(2), SO(2), O(3) and BTEX concentrations of 18 residences and 27 schools. These are related to current guidelines of Flanders, Germany, Norway, China and Canada and evaluated with reference to selected similar studies. It was found that indoor sources such as tobacco smoking and carpets, the latter causing re-suspension of dust, are responsible for elevated indoor respirable particulate matter and place school children and residents at risk. Both PM2.5 and PM10 equalled or exceeded the current guidelines adopted by Flanders, noting that 12-h and 24-h PM2.5 were compared with an annual limit value. Indoor and ambient NO(2) concentrations in the school campaign were higher than the annual EU ambient norm. The other studied pollutant levels were below the current guidelines.     

Seasonal variation in outdoor,indoor, and personal air pollution exposures of women using wood stoves in the Tibetan Plateau: Baseline assessment for an energy intervention study

Cooking and heating with coal and biomass is the main source of household air pollution in China and a leading contributor to disease burden. As part of a baseline assessment for a household energy intervention program, we enrolled 205 adult women cooking with biomass fuels in Sichuan, China and measured their 48-h personal exposure to fine particulate matter (PM_2.5) and carbon monoxide (CO) in winter and summer. We also measured the indoor 48-h PM_2.5 concentrations in their homes and conducted outdoor PM_2.5 measurements during 101 (74) days in summer (winter). Indoor concentrations of CO and nitrogen oxides (NO, NO₂) were measured over 48-h in a subset of ~ 80 homes. Women's geometric mean 48-h exposure to PM_2.5 was 80 μg/m³ (95% CI: 74, 87) in summer and twice as high in winter (169 μg/m³ (95% CI: 150, 190), with similar seasonal trends for indoor PM_2.5 concentrations (winter: 252 μg/m³; 95% CI: 215, 295; summer: 101 μg/m³; 95% CI: 91, 112). We found a moderately strong relationship between indoor PM_2.5 and CO (r = 0.60, 95% CI: 0.46, 0.72), and a weak correlation between personal PM_2.5 and CO (r = 0.41, 95% CI: − 0.02, 0.71). NO₂/NO ratios were higher in summer (range: 0.01 to 0.68) than in winter (range: 0 to 0.11), suggesting outdoor formation of NO₂ via reaction of NO with ozone is a more important source of NO₂ than biomass combustion indoors. The predictors of women's personal exposure to PM_2.5 differed by season. In winter, our results show that primary heating with a low-polluting fuel (i.e., electric stove or wood-charcoal) and more frequent kitchen ventilation could reduce personal PM_2.5 exposures. In summer, primary use of a gaseous fuel or electricity for cooking and reducing exposure to outdoor PM_2.5 would likely have the greatest impacts on personal PM_2.5 exposure.     

Personal exposure monitoring to nitrogen dioxide

Measurement of personal exposure to nitrogen dioxide for short and long term was made with a sensitive NO₂ passive sampler by volunteer housewives and office workers in different seasons. These measurements were compared with the simultaneous measurement of outdoor and indoor concentration of the participants. A common result over all the measurements is the potential effect of using an unvented space heater to increase personal exposure. Mean personal exposure and indoor concentration are higher than outdoor levels elevated by the samples exposed to pollutant produced from the heater. Without an NO₂ source indoors, the mean outdoor concentrations are always highest among the data of measurement. A time-weighted indoor/outdoor activity model gives modestly improved estimates of personal exposure over those predicted from measured indoor concentrations alone.     

Modeling indoor air pollution of outdoor origin in homes of SAPALDIA subjects in Switzerland

Given the shrinking spatial contrasts in outdoor air pollution in Switzerland and the trends toward tightly insulated buildings, the Swiss Cohort Study on Air Pollution and Lung and Heart Diseases in Adults (SAPALDIA) needs to understand to what extent outdoor air pollution remains a determinant for residential indoor exposure. The objectives of this paper are to identify determining factors for indoor air pollution concentrations of particulate matter (PM), ultrafine particles in the size range from 15 to 300 nm, black smoke measured as light absorbance of PM (PM_absorbance) and nitrogen dioxide (NO₂) and to develop predictive indoor models for SAPALDIA. Multivariable regression models were developed based on indoor and outdoor measurements among homes of selected SAPALDIA participants in three urban (Basel, Geneva, Lugano) and one rural region (Wald ZH) in Switzerland, various home characteristics and reported indoor sources such as cooking. Outdoor levels of air pollutants were important predictors for indoor air pollutants, except for the coarse particle fraction. The fractions of outdoor concentrations infiltrating indoors were between 30% and 66%, the highest one was observed for PM_absorbance. A modifying effect of open windows was found for NO₂ and the ultrafine particle number concentration. Cooking was associated with increased particle and NO₂ levels. This study shows that outdoor air pollution remains an important determinant of residential indoor air pollution in Switzerland.     

Indoor air quality modeling: Compartmental approach with reactive chemistry

Data on indoor/outdoor pollutant and tracer concentrations were collected during different periods in 1981 at a residence in Newton, MA. Special studies within the kitchen were conducted to determine the vertical and horizontal variability of pollutant and tracer gas concentrations. A reactive chemistry model incorporating simplified NO_x chemistry was developed to simulate pollutant concentrations indoors. Multicompartmental mathematical modeling tools were also developed and tested to estimate efficiently the effective, emission, ventilation, and removal rates, as well as the intercompartmental pollutant exchange coefficients. Model studies utilizing two- and three-compartment systems and tracer measurements proved that the dynamics of pollutant mixing inside a kitchen is not only complex but may be quite important in controlling spatial and temporal variability of reactive species. Further monitoring and modeling studies to investigate the critical aspects of the short-term dynamics of the reactive pollutants inside homes with gas cooking stoves are recommended.     

Personal monitoring for nitrogen dioxide exposure: Methodological considerations for a community study

Personal exposure to nitrogen dioxide (NO₂) and time spent in various locations were measured for 66 family members from 19 homes in the Portage, WI area during March 1981. Passive diffusion NO₂ monitors were placed outdoors, in the kitchen, and in one bedroom on each floor of the homes, and were worn by family members. Individuals from gas-cooking homes had significantly higher average NO₂ exposures than those from homes using electricity for cooking (mean difference 19.37 μg/m³). Personal exposures were more closely related to bedroom levels than to kitchen or outdoor concentrations for both cooking fuel groups. Several preliminary models are presented which relate average personal NO₂ exposure to indoor and ambient levels, and also to the proportion of time spent in different locations. These models are capable of explaining nearly 90% of the variation about the mean in personal exposure.     

Relationships among personal,indoor and outdoor NO2 measurements

Using integrating NO₂ diffusion dosimeters, personal, indoor and outdoor exposures were measured for nine families in Topeka, Kansas. NO₂ exposures in homes that used gas for cooking were clearly different from those in homes that used electricity. The gas-cooking homes had indoor levels three times the outdoor levels. Members of the gas-cooking households had levels twice those of electric-cooking families and twice the outdoor levels. A linear model that includes outdoor concentrations and stove types explains 77% of the variance in observed NO₂ exposure. The differential NO₂ exposures in homes with and without gas stoves should be considered in epidemiologic studies of the health effects of air pollution.     

Carbon monoxide levels in microenvironment types of four U.S. cities

Portable monitors were used to measure time-averaged personal exposure (10–30 min) to carbon monoxide. Data were collected from January through March 1981 in four cities where ambient carbon monoxide levels have been reported in excess of National Ambient Air Quality Standards: Stamford, CT; Los Angeles, CA; Phoenix, AZ; and Denver, CO. In each city, personal exposure were measured in three common microenvironment types (indoor, commuting, and residential driving) near fixed stations monitoring ambient levels of carbon monoxide. Measurements recorded at urban-residential fixed monitoring stations (excluding one station in Stamford) underrepresented the time-weighted mean of commuting and residential driving exposures by factors of 0.4 to 0.7. The highest mean commuting and residential driving exposures were found in Los Angeles (16.1 and 7.6 μL/L, respectively). Fixed monitoring stations in Los Angeles, Phoenix, and one station in Stamford overrepresented the time-weighted mean of indoor exposures by factors of 1.1 to 1.3. However, in Denver and another station in Stamford, urban stations underrepresented the mean of indoor exposures by factors of 0.4 to 0.8. The highest mean indoor exposure, 5.9 μL/L, was in Denver. In all four cities, regressing personal exposures on concurrent fixed-site concentrations for all recorded values and for values recorded during 8-h NAAQS exceedance time periods revealed no conclusive linear relationships.     

Indoor radon concentrations

The indoor air of 60 residences in and around a Maryland suburb of Washington, DC, was monitored in a pilot study to determine residential radon concentrations. In each residence, a radon grab sample was acquired in the living room, and, if possible, in the basement. Infiltration rates were determined by tracer gas dilution. To help standardize sampling conditions, each home remained closed up for 8 h prior to sampling and during analysis. Over 60% of the residences sampled showed air infiltration rates below 0.6 air changes per hour. Approximately 55% of all surveyed basements and 30% of all surveyed living areas displayed radon concentrations in excess of 4.0 nCi m⁻³. Assuming an equilibrium factor of 0.5, these radon levels may lead to working levels above the annual guidelines suggested by EPA for florida homes build on land reclaimed from phosphate mining.     

The effects of ventilation on residential air pollution due to emissions from a gas-fired range

The use of indoor combustion appliances can cause an increase in the levels of many different pollutants. The work presented here shows the usefulness of a model for extrapolating environmental chamber results on pollutant emissions from combustion appliances to determine indoor pollutant concentrations in actual residences. In addition, the effects of infiltration, whole-house ventilation, and spot ventilation on pollutant levels are investigated. The results show that a range hood is the most effective means of removing pollutants emitted from a gas-fired range; removal rates varied from 60% to 87%.     

北京、上海两地2004和2005年大气污染特征对比分析

为了解北京、上海两市大气污染的变化及其影响因素之间的关系,根据2004、2005年大气质量监测数据,分析了北京、上海两地大气污染特征和两地主要大气污染物的变化规律.结果表明,2004、2005年北京市的PM10最大值是最小值的63.7倍,北京市的变化幅度较上海市的变化幅度大;2004、2005年北京市的SO2最大值是最小值的46.7倍,上海市的SO2最大值是最小值的13.1倍,上海市的SO2污染的因素变化幅度较小;两市的NO2浓度都较高,且季节变化不太明显;两市NO2浓度年平均值满足国家空气质量二级标准,但质量浓度都较高,这与两市的机动车尾气污染有关;两市SO2浓度年平均值除上海市2005年外均满足国家空气质量二级标准,上海市SO2污染严重与上海市消耗大量煤炭有关,北京市SO2污染物浓度年度变化剧烈与冬季取暖烧煤有关;两市可吸入颗粒物污染比较严重,北京市PM10浓度年平均值超过国家空气质量二级标准,上海市PM10浓度年平均值达到国家空气质量二级标准.总体上上海市的大气质量要好于北京市.两地大气主要污染物随时间的变化规律与两地的污染物来源、地理、气候等条件有关.     

Comparisons of elements and inorganic compounds inside and outside of residences

The results of more than 1 yr of air monitoring inside and outside of five homes in each of two communities are presented for SO₂, NO₂, mass respirable particles, SO₄, Al, Br, Cl, Mn, Na, and V. Outdoor measurements across the home site in each city are consistent with proximity to outdoor sources. Looking across indoor residential sites in each city, the home appears to alter outdoor concentrations in several ways. Indoor level of SO₂, SO₄, Mn, and V are lower than those measured outdoors. These constituents are thought generally to result from outdoor sources. The other constituents studied are at times found in excess within homes. In some cases the source or sources of excess concentration of a particular constituent could be identified; often, however, the source of excess indoor concentration could not be identified.     

Estimating the total exposure to air pollutants for different population age groups in Hong Kong

Given that Hong Kong is one of the most densely populated cities in the world, the exposure of the Hong Kong people is one of the interesting research areas. In this study, an indirect approach was used to estimate the exposure to nitrogen dioxide (NO2), respiratory dust (PM10) and carbon monoxide (CO) pollutants experienced by different age groups of people in Hong Kong. The average concentrations of the 20 major microenvironments obtained from our measurement survey data, together with the people activity pattern data obtained from 7-day recall questionnaires, were used to predict frequency distributions to exposure assessment. Our results showed that Hong Kong people spent more than 86% of their time indoors. Homes were shown to be the one of the major exposure sites to NO2, CO and PM10 for all age groups. Our results also indicate that the 24-h NO2 exposure for individuals, irrespective of age, spending more than 2 h in commuting daily, was observed to be exceeding the 24-h NO2 exposure standards. This study was one of the pioneering studies with valuable contribution for modeling the estimates of exposures to NO2, PM10 and CO of different age groups in Hong Kong.     

北京、上海两地2004和2005年大气污染特征对比分析

为了解北京、上海两市大气污染的变化及其影响因素之间的关系,根据2004、2005年大气质量监测数据,分析了北京、上海两地大气污染特征和两地主要大气污染物的变化规律。结果表明,2004、2005年北京市的PM10最大值是最小值的637倍,北京市的变化幅度较上海市的变化幅度大;2004、2005年北京市的SO2最大值是最小值的467倍,上海市的SO2最大值是最小值的131倍,上海市的SO2污染的因素变化幅度较小;两市的NO2浓度都较高,且季节变化不太明显;两市NO2浓度年平均值满足国家空气质量二级标准,但质量浓度都较高,这与两市的机动车尾气污染有关;两市SO2浓度年平均值除上海市2005年外均满足国家空气质量二级标准,上海市SO2污染严重与上海市消耗大量煤炭有关,北京市SO2污染物浓度年度变化剧烈与冬季取暖烧煤有关;两市可吸入颗粒物污染比较严重,北京市PM10浓度年平均值超过国家空气质量二级标准,上海市PM10浓度年平均值达到国家空气质量二级标准。总体上上海市的大气质量要好于北京市。两地大气主要污染物随时间的变化规律与两地的污染物来源、地理、气候等条件有关。     

A preliminary study of ozone trend and its impact on environment in Hong Kong

As far as the impact of air pollutants on human health being is concerned, ozone (O3) is one of the most pollutant sources, and, in particular, the ground level ozone is responsible for a variety of adverse effects on both human being and plant life. To protect the population from such adverse health effects, early information and precautions about the high ozone level need to be ascertained. In this study, statistical characteristics of ground level ozone is analyzed according to field monitoring data in mixed residential, commercial and industrial areas, e.g., Tsuen Wan area in Hong Kong. The study deals with the characteristics of hourly and daily mean ozone levels under different climatic conditions such as temperature, solar radiation (SR), wind speed (WS), and other pollutant concentration levels. The study aims to investigate the importance of meteorological factors and their impact on relevant pollutant concentration levels from a chemical aspect. Further, reasons for the spatial and temporal variation of ozone levels are discussed. All these results will provide a physical basis for accurately predicting ozone concentration in similar research.     

Measurements and analysis of criteria pollutants in New Delhi, India

Ambient concentrations of carbon monoxide (CO), nitrogen oxides (NOx), sulfur dioxide (SO2), and total suspended particulates (TSP) were measured from January 1997 to November 1998 in the center of downtown [the Income Tax Office (ITO) located on B.S.G. Marg] New Delhi, India. The data consist of 24-h averages of SO2, NOx, and TSP as well as 8 and 24-h averages of CO. The measurements were made in an effort to characterize air pollution in the urban environment of New Delhi and assist in the development of an air quality index. The yearly average CO, NOx, SO2, and TSP concentrations for 1997 and 1998 were found to be 4810+/-2287 and 5772+/-2116 microg/m3, 83+/-35 and 64+/-22 microg/m3, 20+/-8 and 23+/-7 microg/m3, and 409+/-110 and 365+/-100 microg/m3, respectively. In general, the maximum CO, SO2, NOx, and TSP values occurred during the winter with minimum values occurring during the summer, which can be attributed to a combination of meteorological conditions and photochemical activity in the region. The ratio of CO/NOx (approximately 50) indicates that mobile sources are the predominant contributors for these two compounds in the urban air pollution problem in New Delhi. The ratio of SO2/NOx (approximately 0.6) indicates that point sources are contributing to SO2 pollution in the city. The averaged background CO concentrations in New Delhi were also calculated (approximately 1939 microg/m3) which exceed those for Eastern USA (approximately 500 microg/m3). Further, all measured concentrations exceeded the US National Ambient Air Quality Standards (NAAQS) except for SO2. TSP was identified as exceeding the standard on the most frequent basis.     

Air pollutant exposure and preterm and term small-for-gestational-age births in Detroit,Michigan: Long-term trends and associations

Studies in a number of countries have reported associations between exposure to ambient air pollutants and adverse birth outcomes, including low birth weight, preterm birth (PTB) and, less commonly, small for gestational age (SGA). Despite their growing number, the available studies have significant limitations, e.g., incomplete control of temporal trends in exposure, modest sample sizes, and a lack of information regarding individual risk factors such as smoking. No study has yet examined large numbers of susceptible individuals.We investigated the association between ambient air pollutant concentrations and term SGA and PTB outcomes among 164,905 singleton births in Detroit, Michigan occurring between 1990 and 2001. SO₂, CO, NO₂, O₃ and PM₁₀ exposures were used in single and multiple pollutant logistic regression models to estimate odds ratios (OR) for these outcomes, adjusted for the infant's sex and gestational age, the mother's race, age group, education level, smoking status and prenatal care, birth season, site of residence, and long-term exposure trends.Term SGA was associated with CO levels exceeding 0.75 ppm (OR = 1.14, 95% confidence interval = 1.02–1.27) and NO₂ exceeding 6.8 ppb (1.11, 1.03–1.21) exposures in the first month, and with PM₁₀ exceeding 35 μg/m³ (1.22, 1.03–1.46) and O₃ (1.11, 1.02–1.20) exposure in the third trimester. PTB was associated with SO₂ (1.07, 1.01–1.14) exposure in the last month, and with (hourly) O₃ exceeding 92 ppb (1.08, 1.02–1.14) exposure in the first month.Exposure to several air pollutants at modest concentrations was associated with adverse birth outcomes. This study, which included a large Black population, suggests the importance of the early period of pregnancy for associations between term SGA with CO and NO₂, and between O₃ with PTB; and the late pregnancy period for associations between term SGA and O₃ and PM₁₀, and between SO₂ with PTB. It also highlights the importance of accounting for individual risk factors such as maternal smoking, maternal race, and long-term trends in air pollutant levels and adverse birth outcomes in evaluating relationships between pollutant exposures and adverse birth outcomes.     

Temporal variation of 212Pb concentration in outdoor air of Milan and a comparison with 214Bi

Continuous measurement of hourly concentrations of 212Pb attached to aerosol particles was carried out during the whole year 2000 in the outdoor air of Milan (Italy). An improved experimental method based on on-line alpha spectroscopy during atmospheric particulate matter sampling allowed the contemporary determination of 212Pb and 214Bi through the deconvolution of the alpha energy spectral distribution analysis. The 212Pb hourly concentrations were about 100 times lower than 214Bi but showed a similar characteristic diurnal time trend. However, the influence of meteorological parameters such as rain and wind was more evident in 212Pb than in 214Bi concentrations. The 212Pb average annual concentration was 0.090 +/- 0.060 Bq/m3 with daily mean concentration varying from 0.013 to 0.333 Bq/m3.