Installation of platform screen doors and their impact on indoor air quality: Seoul subway trains

In this study, variations of particulate matter (PM) concentrations in subway trains following installation of platform screen doors (PSDs) in the Seoul subway system were investigated. PM samples were collected in the trains on subway lines 1–8 before and after installation of PSDs. It was found that the mean PM₁₀ concentration in the trains after PSDs installation increased significantly by 29.9% compared to that before installation. In particular, the increase of PM₁₀ in line 6 was the highest at 103%. When the relationship between PM₁₀ and PM_2.5 was compared, coefficients of determination (r²) before and after PSDs installations were 0.696 and 0.169, respectively. This suggests that air mixing between the platform and the tunnel after PSDs installation was extremely restricted. In addition, the indoor/outdoor PM₁₀ ratio following PSDs installation increased from 1.32 to 2.97 relative to the period with no installed PSDs. Furthermore, this study revealed that PM levels in subway trains increased significantly after all underground PSDs were put in use. Several potential factors were examined that could result in this PM increase, such as train ventilation systems, operational conditions, passenger volume, subway depth, and the length of underground segments.

ImplicationsPM₁₀ concentrations inside the subway trains increased after PSDs installation. This indicates that air quality in trains was very seriously impacted by PSDs. PM₁₀ levels were also influenced by the tunnel depth and length of the underground segments. To prevent the adverse effect on human health by PM₁₀ emitted from the tunnel, an applicable ventilation system to reduce PM₁₀ is required inside trains and tunnels.     

Identification of the sources of PM10 in a subway tunnel using positive matrix factorization

The level of particulate matter of less than 10 μm diameter (PM₁₀) at subway platforms can be significantly reduced by installing a platform screen-door system. However, both workers and passengers might be exposed to higher PM₁₀ levels while the cars are within the tunnel because it is a more confined environment. This study determined the PM₁₀ levels in a subway tunnel, and identified the sources of PM₁₀ using elemental analysis and receptor modeling. Forty-four PM₁₀ samples were collected in the tunnel between the Gireum and Mia stations on Line 4 in metropolitan Seoul and analyzed using inductively coupled plasma–atomic emission spectrometry and ion chromatography. The major PM₁₀ sources were identified using positive matrix factorization (PMF). The average PM₁₀ concentration in the tunnels was 200.8 ± 22.0 μg/m³. Elemental analysis indicated that the PM₁₀ consisted of 40.4% inorganic species, 9.1% anions, 4.9% cations, and 45.6% other materials. Iron was the most abundant element, with an average concentration of 72.5 ± 10.4 μg/m³. The PM₁₀ sources characterized by PMF included rail, wheel, and brake wear (59.6%), soil combustion (17.0%), secondary aerosols (10.0%), electric cable wear (8.1%), and soil and road dust (5.4%). Internal sources comprising rail, wheel, brake, and electric cable wear made the greatest contribution to the PM₁₀ (67.7%) in tunnel air.

ImplicationsWith installation of a platform screen door, PM₁₀ levels in subway tunnels were higher than those on platforms. Tunnel PM₁₀ levels exceeded 150 μg/m³ of the Korean standard for subway platform. Elemental analysis of PM₁₀ in a tunnel showed that Fe was the most abundant element. Five PM₁₀ sources in tunnel were identified by positive matrix factorization. Railroad-related sources contributed 68% of PM₁₀ in the subway tunnel.     

Concentrations,properties, and health risk of PM2.5 in the Tianjin City subway system

A campaign was conducted to assess and compare the personal exposure in L3 of Tianjin subway, focusing on PM_2.5 levels, chemical compositions, morphology analysis, as well as the health risk of heavy metal in PM_2.5. The results indicated that the average concentration of the PM_2.5 was 151.43 μg/m³ inside the train of the subway during rush hours. PM_2.5 concentrations inside car under the ground are higher than those on the ground, and PM_2.5 concentrations on the platform are higher than those inside car. Regarding metal concentrations, the highest element in PM_2.5 samples was Fe; the level of which is 17.55 μg/m³. OC is a major component of PM_2.5 in Tianjin subway. Secondary organic carbon is the formation of gaseous organic pollutants in subway. SEM–EDX and TEM–EDX exhibit the presence of individual particle with a large metal content in the subway samples. For small Fe metal particles, iron oxide can be formed easily. With regard to their sources, Fe-containing particles are generated mainly from mechanical wear and friction processes at the rail–wheel–brake interfaces. The non-carcinogenic risk to metals Cr, Ni, Cu, Zn and Pb, and carcinogenic hazard of Cr and Ni were all below the acceptable level in L3 of Tianjin subway.

     

Concentration and characterization of airborne particles in Tehran’s subway system

Particulate matter is an important air pollutant, especially in closed environments like underground subway stations. In this study, a total of 13 elements were determined from PM₁₀ and PM_2.5 samples collected at two subway stations (Imam Khomeini and Sadeghiye) in Tehran’s subway system. Sampling was conducted in April to August 2011 to measure PM concentrations in platform and adjacent outdoor air of the stations. In the Imam Khomeini station, the average concentrations of PM₁₀ and PM_2.5 were 94.4?±?26.3 and 52.3?±?16.5 μg m^?3 in the platform and 81.8?±?22.2 and 35?±?17.6 μg m^?3 in the outdoor air, respectively. In the Sadeghiye station, mean concentrations of PM₁₀ and PM_2.5 were 87.6?±?23 and 41.3?±?20.4 μg m^?3 in the platform and 73.9?±?17.3 and 30?±?15 μg m^?3, in the outdoor air, respectively. The relative contribution of elemental components in each particle fraction were accounted for 43 % (PM₁₀) and 47.7 % (PM_2.5) in platform of Imam Khomeini station and 15.9 % (PM₁₀) and 18.5 % (PM_2.5) in the outdoor air of this station. Also, at the Sadeghiye station, each fraction accounted for 31.6 % (PM₁₀) and 39.8 % (PM_2.5) in platform and was 11.7 % (PM₁₀) and 14.3 % (PM_2.5) in the outdoor. At the Imam Khomeini station, Fe was the predominant element to represent 32.4 and 36 % of the total mass of PM₁₀ and PM_2.5 in the platform and 11.5 and 13.3 % in the outdoor, respectively. At the Sadeghiye station, this element represented 22.7 and 29.8 % of total mass of PM₁₀ and PM_2.5 in the platform and 8.7 and 10.5 % in the outdoor air, respectively. Other major crustal elements were 5.8 % (PM₁₀) and 5.3 % (PM_2.5) in the Imam Khomeini station platform and 2.3 and 2.4 % in the outdoor air, respectively. The proportion of other minor elements was significantly lower, actually less than 7 % in total samples, and V was the minor concentration in total mass of PM₁₀ and PM_2.5 in both platform stations.     

Hydrochemistry of urban groundwater, Seoul, Korea: the impact of subway tunnels on groundwater quality

Hydrogeologic and hydrochemical data for subway tunnel seepage waters in Seoul (Republic of Korea) were examined to understand the effect of underground tunnels on the degradation of urban groundwater. A very large quantity of groundwater (up to 63 million m³ year^− 1) is discharged into subway tunnels with a total length of 287 km, resulting in a significant drop of the local groundwater table and the abandonment of groundwater wells. For the tunnel seepage water samples (n = 72) collected from 43 subway stations, at least one parameter among pathogenic microbes (total coliform, heterotrophic bacteria), dissolved Mn and Fe, NH₄⁺, NO₃⁻, turbidity, and color exceeded the Korean Drinking Water Standards. Locally, tunnel seepage water was enriched in dissolved Mn (avg. 0.70 mg L^− 1, max. 5.58 mg L^− 1), in addition to dissolved Fe, NH₄⁺, and pathogenic microbes, likely due to significant inflow of sewage water from broken or leaking sewer pipes.Geochemical modeling of redox reactions was conducted to simulate the characteristic hydrochemistry of subway tunnel seepage. The results show that variations in the reducing conditions occur in urban groundwater, dependent upon the amount of organic matter-rich municipal sewage contaminating the aquifer. The organic matter facilitates the reduction and dissolution of Mn- and Fe-bearing solids in aquifers and/or tunnel construction materials, resulting in the successive increase of dissolved Mn and Fe. The present study clearly demonstrates that locally significant deterioration of urban groundwater is caused by a series of interlinked hydrogeologic and hydrochemical changes induced by underground tunnels.     

Quantitative ED-EPMA combined with morphological information for the characterization of individual aerosol particles collected in Incheon,Korea

A quantitative single-particle analytical technique, called low-Z particle electron probe X-ray microanalysis, combined with the utilization of their morphological information on individual particles, was applied to characterize six aerosol samples collected in one Korean city, Incheon, during March 9–15, 2006. The collected supermicron aerosol particles were classified based on their chemical species and morphology on a single-particle basis. Many different particle types were identified and their emission source, transport, and reactivity in the air were elucidated. In the samples, particles in the “soil-derived particles” group were the most abundant, followed by “reacted sea-salts”, “reacted CaCO₃-containing particles”, “genuine sea-salts”, “reacted sea-salts + others”, “Fe-containing particles”, “anthropogenic organics”, (NH₄)₂SO₄, “K-containing particles”, and “fly ash”. The application of this single-particle analysis, fully utilizing their chemical compositional and morphological data of individual particles, clearly revealed the different characteristics of the six aerosol samples. For samples S3 and S5, which were sampled during two Asian dust storm events, almost all particles were of soil origin that had not experienced chemical modification and that did not entrain sea-salts during their long-range transport. For sample S1, collected at an episodic period of high PM₁₀ concentration and haze, anthropogenic, secondary, and soil-derived particles emitted from local sources were predominant. For samples S2, S4, and S6, which were collected on average spring days with respect to their PM₁₀ concentrations, marine originated particles were the most abundant. Sample S2 seems to have been strongly influenced by emissions from the Yellow Sea and Korean peninsula, sample S4 had the minimum anthropogenic influence among the four samples collected in the absence of any Asian dust storm event, and sample S6 seems to have entrained air pollutants that had been transported from mainland China over the Yellow Sea to Korea.     

Dust build-up on surfaces in the indoor environment

The concentration and the composition of dust in the indoor environment has been associated with reported symptoms of the sick building syndrome. Levels of airborne concentrations of dust particles are well known. However, the relation to dust on surfaces for office environments are not well described. In this study, 662 measurements were performed of surface dust concentrations on hard surfaces in 19 buildings within Harvard University based on a sticking gelatine foil method. The measure is the dust covered area of the surface as a percentage. In three offices, the build-up of dust on surfaces was measured for a period of five days. Close to these surfaces the airborne PM_2.5 and PM₁₀ particle mass concentrations were measured simultanously. A significant correlation between the dust build-up and the difference between the PM₁₀ and the PM_2.5 was established. The particle size distribution was measured by means of an Aerodynamic Particle Sizer. The mean dust build-up normalized with the measured PM₁₀ was approximately four times higher than the equivalent calculated by a deposition model. This may in part be due to the effect of preferred orientation when particles settle to a surface. Different data for dust on surfaces and airborne particles in offices were compared. The levels of airborne particles in offices in Europe seem to be higher than the levels in the US.     

Experimental evidence for a significant contribution of cellulose to indoor aerosol mass concentration

An apartment bedroom located in a residential area of Aveiro (Portugal) was selected with the aim of characterizing the cellulose content of indoor aerosol particles. Two sets of samples were taken: (1) PM₁₀ collected simultaneously in indoor and outdoor air; (2) PM₁₀ and PM_2.5 collected simultaneously in indoor air. The aerosol particles were concentrated on quartz fibre filters with low-volume samplers equipped with size selective inlets. The filters were weighed and then extracted for cellulose analysis by an enzymatic method. The average indoor cellulose concentration was 1.01 ± 0.24 μg m^?3, whereas the average outdoor cellulose concentration was 0.078 ± 0.047 μg m^?3, accounting for 4.0% and 0.4%, respectively, of the PM₁₀ mass. The corresponding average ratio between indoor and outdoor cellulose concentrations was 11.1 ± 4.9, indicating that cellulose particles were generated indoors, most likely due to the handling of cotton-made textiles as a result of routine daily activities in the bedroom. Indoor cellulose concentrations averaged 1.22 ± 0.53 μg m^?3 in the aerosol coarse fraction (determined from the difference between PM₁₀ and PM_2.5 concentrations) and averaged 0.38 ± 0.13 μg m^?3 in the aerosol fine fraction. The average ratio between the coarse and fine fractions of cellulose concentrations in the indoor air was 3.6 ± 2.1. This ratio is in line with the primary origin of this biopolymer. Results from this study provide the first experimental evidence in support of a significant contribution of cellulose to the mass of suspended particles in indoor air.     

A functional group characterization of organic PM2.5 exposure: Results from the RIOPA study

The functional group (FG) composition of urban residential outdoor, indoor, and personal fine particle (PM_2.5) samples is presented and used to provide insights relevant to organic PM_2.5 exposure. PM_2.5 samples (48 h) were collected during the Relationship of Indoor, Outdoor, and Personal Air (RIOPA) study at 219 non-smoking homes (once or twice) in Los Angeles County, CA, Elizabeth, NJ, and Houston, TX. Fourier transform infrared (FTIR) spectra of PM_2.5 samples were collected, and FG absorbances were quantified by partial least squares (PLS) regression, a multivariate calibration method.There is growing evidence in the literature that a large majority of indoor-generated PM_2.5 is organic. The current research suggests that indoor-generated PM_2.5 is enriched in aliphatic carbon–hydrogen (CH) FGs relative to ambient outdoor PM_2.5. Indoor-generated CH exceeded outdoor-generated CH in 144 of the 167 homes for which indoor or outdoor CH was measurable; estimated indoor emission rates are provided. The strong presence of aliphatic CH FGs in indoor PM_2.5 makes particulate organic matter substantially less polar indoors and in personal exposures than outdoors. This is a substantial new finding. Based on the quantified FGs, the average organic molecular weight (OM) per carbon weight (OC), a measure of the degree of oxygenation of organic PM, is in the range of 1.7–2.6 for outdoor samples and 1.3–1.7 for indoor and personal samples. Polarity or degree of oxygenation effects particle deposition in exposure environments and in the respiratory system.     

Associations between particle physicochemical characteristics and oxidative capacity: An indoor PM10 study in Beijing,China

A study was undertaken to determine the use of a plasmid DNA scission assay to evaluate the causal relationships between particle oxidative capacity and physico-chemistry. Field emission scanning electron microscopy (FESEM), image analysis (IA) and inductively coupled plasma-mass spectrometry (ICP-MS) were employed to investigate the physico-chemical characteristics of indoor PM₁₀ (particulate matter with an aerodynamic diameter of 10 μm or less) in Beijing, China. Six PM₁₀ samples (indoor smoker's living room; indoor non-smoker's living room and kitchen; and outdoor Beijing city; winter versus summer) were selected to represent typical indoor Beijing PM₁₀ environments that contain high particle mass. The PM₁₀ collected from a kitchen and two smoker's homes had the lowest TD₅₀ (toxic dosage of PM₁₀ causing 50% plasmid DNA damage), being as low as 45 μg ml⁻¹ (kitchen) and 100 μg ml⁻¹ (living room), which suggests a high oxidative capacity, with the PM₁₀ generated in kitchens appearing to be the most toxic. The indoor PM₁₀ from the non-smoker's home and outdoor PM₁₀ samples demonstrated high TD₅₀ values and were deemed less bioreactive (i.e. caused limited DNA damage). FESEM observations revealed that four types of particle species were prevalent in Beijing indoor PM₁₀; soot aggregates, minerals, coal fly ash and unknown fine particles. IA showed that higher percentages of soot and unknown fine particles were associated with the lower TD₅₀ values, suggesting that soot and the unknown fine particles may be important components responsible for the observed plasmid DNA damage. The water-soluble trace elements were negatively correlated with the TD₅₀ values, implying that the DNA damage may be attributed to the water-soluble fraction of the PM₁₀. Water-soluble zinc revealed the best relationship with the TD₅₀ values than other analyzed elements, signifying it may play a role in driving the oxidative damage.     

Effect of combustion condition on cytotoxic and inflammatory activity of residential wood combustion particles

Residential heating is an important local source of fine particles and may cause significant exposure and health effects in populations. We investigated the cytotoxic and inflammatory activity of particulate emissions from normal (NC) and smouldering (SC) combustion in one masonry heater. The PM_1–0.2 and PM_0.2 samples were collected from the dilution tunnel with a high-volume cascade impactor (HVCI). Mouse RAW 264.7 macrophages were exposed to the PM-samples for 24 h. Inflammatory mediators, (IL-6, TNFα and MIP-2), and cytotoxicity (MTT-test), were measured. Furthermore, apoptosis and cell cycle of macrophages were analyzed. The HVCI particulate samples were characterized for ions, elements and PAH compounds. Assays of elemental and organic carbon were conducted from parallel low volume samples. All the samples displayed mostly dose-dependent inflammatory and cytotoxic activity. SC samples were more potent than NC samples at inducing cytotoxicity and MIP-2 production, while the order of potency was reversed in TNFα production. SC-PM_1–0.2 sample was a significantly more potent inducer of apoptosis than the respective NC sample. After adjustment for the relative toxicity with emission factor (mg MJ^?1), the SC-PM emissions had clearly higher inflammatory and cytotoxic potential than the NC-PM emissions. Thus, operational practice in batch burning of wood and the resultant combustion condition clearly affect the toxic potential of particulate emissions.     

Inter-comparison of air pollutant concentrations in different indoor environments in Hong Kong

Indoor air quality in selected indoor environments in Hong Kong such as homes, offices, schools, shopping malls and restaurants were investigated. Average CO₂ levels and total bacteria counts in air-conditioned classrooms, shopping malls and restaurants were comparatively higher than those measured in occupied offices and homes. Elevated CO₂ levels exceeding 1000 ppm and total bacteria counts resulted from high occupancy combined with inadequate ventilation. Average PM₁₀ levels were usually higher indoors than outdoors in homes, shopping malls and restaurants. The highest indoor PM₁₀ levels were observed at investigated restaurants due to the presence of cigarette smoking and extensive use of gas stoves for cooking. The restaurants and shopping malls investigated had higher formaldehyde levels than other indoor environments when building material, smoking and internal renovation work were present. Volatile organic compounds (VOCs) in both indoor and outdoor environments mainly resulted from vehicle exhaust emissions. It was observed that interior decoration work and the use of industrial solvents in an indoor environment could significantly increase the indoor levels of VOCs.     

Indoor particulate matter in urban residences of Alexandria,Egypt

Indoor particulate matter samples were collected in 17 homes in an urban area in Alexandria during the summer season. During air measurement in all selected homes, parallel outdoor air samples were taken in the balconies of the domestic residences. It was found that the mean indoor PM_2.5 and PM₁₀ (particulate matter with an aerodynamic diameter ≤2.5 and ≤10 μm, respectively) concentrations were 53.5 ± 15.2 and 77.2 ± 15.1 µg/m³, respectively. The corresponding mean outdoor levels were 66.2 ± 16.5 and 123.8 ± 32.1 µg/m³, respectively. PM_2.5 concentrations accounted, on average, for 68.8 ± 12.8% of the total PM₁₀ concentrations indoors, whereas PM_2.5 contributed to 53.7 ± 4.9% of the total outdoor PM₁₀ concentrations. The median indoor/outdoor mass concentration (I/O) ratios were 0.81 (range: 0.43–1.45) and 0.65 (range: 0.4–1.07) for PM_2.5 and PM₁₀, respectively. Only four homes were found with I/O ratios above 1, indicating significant contribution from indoor sources. Poor correlation was seen between the indoor PM₁₀ and PM_2.5 levels and the corresponding outdoor concentrations. PM₁₀ levels were significantly correlated with PM_2.5 loadings indoors and outdoors and this might be related to PM₁₀ and PM_2.5 originating from similar particulate matter emission sources. Smoking, cooking using gas stoves, and cleaning were the major indoor sources contributed to elevated indoor levels of PM₁₀ and PM_2.5.

Implications: The current study presents results of the first PM_2.5 and PM₁₀ study in homes located in the city of Alexandria, Egypt. Scarce data are available on indoor air quality in Egypt. Poor correlation was seen between the indoor and outdoor particulate matter concentrations. Indoor sources such as smoking, cooking, and cleaning were found to be the major contributors to elevated indoor levels of PM₁₀ and PM_2.5.     

Source Apportionment of Particulate Matter (PM10) and Indoor Dust in a University Building

A study on source apportionment of indoor dust and particulate matter (PM₁₀) composition was conducted in a university building by using chemometrics. The objective of this study was to investigate the potential sources of selected heavy metals and ionic species in PM₁₀ and indoor dust. PM₁₀ samples were collected using a low-volume sampler (LVS) and indoor dust was collected using a soft brush. Inductively coupled plasma spectrometry (ICP-MS) was used to determine the concentration of heavy metals, while the concentration of cations and anions was determined by atomic absorption spectrometer (AAS) and ion chromatography (IC), respectively. The concentration of PM₁₀ recorded in the building throughout the sampling period ranged from 20 ± 10 μgm^?3 to 80 ± 33 μgm^?3. The composition of heavy metals in PM₁₀ and indoor dust were dominated by zinc (Zn), followed by lead (Pb), copper (Cu), and cadmium (Cd). Principle component analysis (PCA) and multiple linear regression (MLR) showed that the main sources of pollutants in PM₁₀ came from indoor renovations (73.83%), vehicle emissions (16.38%), earth crust sources (9.68%), and other outdoor sources (0.11%). For indoor dust, the pollutant source was mainly earth crust. This study suggests that chemometrics can be used for forensic investigation to determine the possible sources of indoor contaminants within a public building.     

Properties and sources of individual particles and some chemical species in the aerosol of a metropolitan underground railway station

Aerosol samples in PM_10–2.0 and PM_2.0 size fractions were collected on the platform of a metropolitan underground railway station in central Budapest. Individual aerosol particles were studied using atomic force microscopy, scanning electron microscopy and transmission electron microscopy with energy-dispersive X-ray spectrometry and electron diffraction. The bulk aerosol samples were investigated by ⁵⁷Fe Mössbauer spectroscopy, and they were subjected to chemical speciation analysis for Cr. The particles were classified into groups of iron oxides and iron, carbonates, silicates, quartz and carbonaceous debris. Electron micrographs showed that the Fe-rich particles in the PM_2.0 size fraction typically consisted of aggregates of nano-sized hematite crystals that were randomly oriented, had round shapes and diameters of 5–15 nm. In addition to hematite, a minor fraction of the iron oxide particles also contained magnetite. In addition, the PM_2.0-fraction particles typically had a rugged surface with layered or granular morphologies. Mössbauer spectroscopy suggested that hematite was a major Fe-bearing species in the PM_10–2.0 size fraction; its mass contribution to the Fe was 36%. Further constituents (ferrite, carbides and FeOOH) were also identified. The water soluble amounts of Cr for the underground railway station and city center were similar. In the PM_10–2.0 size fraction, practically all dissolved Cr had an oxidation state of three, which corresponds to ambient conditions. In the PM_2.0 size fraction, however, approximately 7% of the dissolved Cr was present as Cr(VI), which was different from that for the urban aerosol. It is suggested that the increased adverse health effects of aerosol particles in metros with respect to ambient outdoor particles is linked to the differences in the oxidation states, surface properties or morphologies.     

Influence of tobacco smoke on the elemental composition of indoor particles of different sizes

Tobacco smoking is one of the greatest sources of indoor inhalable (PM₁₀) particles. In the past, the studies conducted on indoor particulates were mostly related to PM₁₀, however in the last decade respirable particles (PM_2.5) and even smaller particles (PM₁) began to be more important as they penetrate deeper in the respiratory system, causing severe health effects. Therefore, more information on fine particles is needed. Aiming to evaluate the impact of tobacco smoke on public health, this work evaluates the influence of tobacco smoke on the characteristics of PM₁₀, PM_2.5, and PM₁ considering concentration and elemental composition. Samples were collected at sites influenced by tobacco smoke, as well as at reference sites, using low-volume samplers; the element analyses were performed by proton induced X-ray emission (PIXE); Mg, Al, Si, P, S, Cl, K, Ca, Ti, V, Cr, Mn, Fe, Ni, Cu, Zn, As, Se, Br, Cd, I, Ba, La, Ce and Pb were quantified. At the sites influenced by tobacco smoke concentrations were 270–560% higher for PM₁₀ and 320–680% higher for PM_2.5 than at reference sites. Tobacco smoke increased the total concentrations of five carcinogenic elements (Cr, Ni, As, Cd and Pb) 1100–2400% for PM₁₀ and 840–2200% for PM_2.5. The elements associated with tobacco smoke (S, K, Cr, Ni, Zn, As, Cd and Pb) were predominantly present in the fine fraction; the elements mostly originating from building erosion (Mg, Al, Si and Ca) predominantly occurred in the coarse particles. The analysis of enrichment factors confirmed that tobacco smoking mainly influenced the composition of the fine fraction of particles; as these smaller particles have a strong influence on health, these conclusions are relevant for the development of strategies to protect public health.     

Characterization of Indoor Particle Sources Using Continuous Mass and Size Monitors

ABSTRACT

A comprehensive indoor particle characterization study was conducted in nine Boston-area homes in 1998 in order to characterize sources of PM in indoor environments. State-of-the-art sampling methodologies were used to obtain continuous PM_2.5 concentration and size distribution particulate data for both indoor and outdoor air. Study homes, five of which were sampled during two seasons, were monitored over week-long periods. Among other data collected during the extensive monitoring efforts were 24hr elemental/organic carbon (EC/OC) particulate data as well as semi-continuous air exchange rates and time-activity information.

This rich data set shows that indoor particle events tend to be brief, intermittent, and highly variable, thus requiring the use of continuous instrumentation for their characterization. In addition to dramatically increasing indoor PM₂₅ concentrations, these data demonstrate that indoor particle events can significantly alter the size distribution and composition of indoor particles. Source event data demonstrate that the impacts of indoor activities are especially pronounced in the ultrafine (d_a < 0.1 um) and coarse (2.5 < d_a < 10 |um) modes. Among the sources of ultrafine particles characterized in this study are indoor ozone/terpene reactions. Furthermore, EC/OC data suggest that organic carbon is a major constituent of particles emitted during indoor source events. Whether exposures to indoor-generated particles, particularly from large short-term peak events, may be associated with adverse health effects will become clearer when biological mechanisms are better known.     

An assessment of indoor air quality in recent Mexican immigrant housing in Commerce City, Colorado

An indoor air quality assessment was conducted on 100 homes of recent Mexican immigrants in Commerce City, Colorado, an urban industrial community north of Denver. Head of households were administered a family health survey, filled out an activity diary, and participated in a home inspection. Carbon monoxide (CO) and carbon dioxide (CO₂) were measured for 24 h inside the main living area and outside of the homes. Harvard Impactors were used to collect 24-h samples of PM_2.5 at the same locations for gravimetric analysis. Dust samples were collected by vacuuming carpeting and flooring at four locations within the home and analyzed by ELISA for seven allergens. Mean indoor and outdoor PM_2.5 levels were 27.2 and 8.5 μg m⁻³, respectively. Indoor PM_2.5 and CO₂ were elevated in homes for which the number of hours with door/window open was zero compared to homes in which the number of hours was high (>15 h). Indoor PM_2.5 levels did not correlate with outdoor levels and tended to increase with number of inhabitants, and results indicate that the source of indoor particles were occupants and their activities, excluding smoking and cooking. Mean indoor CO₂ and CO levels were 1170 and 2.4 ppm, respectively. Carbon monoxide was higher than the 24-h National Ambient Air Quality Standard in 3 of the homes. The predominant allergens were cat (Fel d 1) and mouse (Mus m 1) allergens, found in 20 and 34 homes, respectively.     

Outdoor and indoor factors influencing particulate matter and carbon dioxide levels in naturally ventilated urban homes

ABSTRACT

The present study investigated indoor and outdoor concentrations of two particulate matter size fractions (PM₁₀ and PM_2.5) and CO₂ in 20 urban homes ventilated naturally and located in one congested residential and commercial area in the city of Alexandria, Egypt. The results indicate that the daily mean PM_2.5 concentrations measured in the ambient air, living rooms, and kitchens of all sampling sites exceeded the WHO guideline by 100%, 65%, and 95%, respectively. The daily mean outdoor and indoor PM₁₀ levels in all sampling sites were found to exceed the WHO guideline by 100% and 80%, respectively. The indoor PM₁₀ and PM_2.5 concentrations were significantly correlated with their corresponding outdoor levels, as natural ventilation through opening doors and windows allowed direct transfer of outdoor airborne particles into the indoor air. Most of the kitchens investigated had higher indoor concentrations of PM_2.5 and CO₂ than in living rooms. The elevated levels of PM_2.5 and CO₂ in domestic kitchens were probably related to inadequate ventilation. The current study attempted to understand the sources and the various indoor and outdoor factors that affect indoor PM₁₀, PM_2.5 and CO₂ concentrations. Several domestic activities, such as smoking, cooking, and cleaning, were found to constitute important sources of indoor air pollution. The indoor pollution caused by PM_2.5 was also found to be more serious in the domestic kitchens than in the living rooms and the results suggest that exposure to PM_2.5 is high and highlights the need for more effective control measures.

Implications: Indoor air pollution is a complex problem that involves many determinant factors. Understanding the relationships and the influence of various indoor and outdoor factors on indoor air quality is very important to prioritize control measures and mitigation action plans. There is currently a lack of research studies in Egypt to investigate determinant factors controlling indoor air quality for urban homes. The present study characterizes the indoor and outdoor concentrations of PM₁₀, PM_2.5, and CO₂ in residential buildings in Alexandria city. The study also determines the indoor and outdoor factors which influence the indoor PM and CO₂ concentrations as well as it evaluates the potential indoor sources in the selected homes. This research will help in the development of future indoor air quality standards for Egypt.     

Non-exhaust emission measurement system of the mobile laboratory SNIFFER

In this paper we describe and quality assure the sampling system of a mobile research laboratory SNIFFER which was shown to be a useful tool for studying emission levels of respirable dust from street surfaces. The dust plume had bimodal structure; another mode rising to higher altitudes whereas the other mode remained at lower altitudes. The system was tested on a route in Helsinki, Finland, during spring 2005 and 2006. The PM_2.5 and PM₁₀ were positively correlated and the PM levels increased with the vehicle speed. SNIFFER was able to identify the characteristic emission levels on different streets. A clear downward trend in the concentrations was observed in all street locations between April and June. The composition of the street dust collected by SNIFFER was compared with springtime PM₁₀ aerosol samples from the air quality monitoring stations in Helsinki. The results showed similarities in the abundance and composition of the mineral fraction but contained significantly more salt particles.