Potential effects of particulate matter from combustion during services on human health and on works of art in medieval churches in Cyprus

Indoor and outdoor particulate matter (PM_0.3-10) number concentrations were established in two medieval churches in Cyprus. In both churches incense was burnt occasionally during Mass. The highest indoor PM_0.5-1 concentrations compared with outdoors (10.7 times higher) were observed in the church that burning of candles indoors was allowed. Peak indoor black carbon concentration was 6.8 μg m⁻³ in the instances that incense was burning and 13.4 μg m⁻³ in the instances that the candles were burning (outdoor levels ranged between 0.6 and 1.3 μg m⁻³). From the water soluble inorganic components determined in PM₁₀, calcium prevailed in all samples indoors or outdoors, whilst high potassium concentration indoors were a clear marker of combustion. Indoor sources of PM were clearly identified and their emission strengths were estimated via modeling of the results. Indoor estimated PM_0.3-10 mass concentrations exceeded air quality standards for human health protection and for the preservation of works of art.     

The transformation of outdoor ammonium nitrate aerosols in the indoor environment

Recent studies associate particulate air pollution with adverse health effects; however, the exposure to indoor particles of outdoor origin is not well characterized, particularly for individual chemical species. We conducted a field study in an unoccupied, single-story residence in Clovis, California to provide data and analyses to address issues important for assessing exposure. We used real-time particle monitors both outdoors and indoors to quantify nitrate, sulfate, and carbon particulate matter of particle size 2.5 μm or less in diameter (PM-2.5). The results show that measured indoor ammonium nitrate concentrations were significantly lower than would be expected based solely on penetration and deposition losses. The additional reduction can be attributed to the transformation indoors of ammonium nitrate into ammonia and nitric acid gases, which are subsequently lost by deposition and sorption to indoor surfaces. A mass balance model that accounts for the kinetics of ammonium nitrate evaporation was able to reproduce measured indoor ammonium nitrate and nitric acid concentrations, resulting in a fitted value of the deposition velocity for nitric acid of 0.56 cm s⁻¹. The results indicate that indoor exposure to outdoor ammonium nitrate in Central Valley of California are small, and suggest that exposure assessments based on total particle mass measured outdoors may obscure the actual causal relationships for indoor exposure to particles of outdoor origin.     

PM2.5, soot and NO2 indoor–outdoor relationships at homes,pre-schools and schools in Stockholm,Sweden

In developed nations people spend about 90% of their time indoors. The relationship between indoor and outdoor air pollution levels is important for the understanding of the health effects of outdoor air pollution. Although other studies describe both the outdoor and indoor atmospheric environment, few excluded a priori major indoor sources, measured the air exchange rate, included more than one micro-environment and included the presence of human activity. PM_2.5, soot, NO₂ and the air exchange rate were measured during winter and summer indoors and outdoors at 18 homes (mostly apartments) of 18 children (6–11-years-old) and also at the six schools and 10 pre-schools that the children attended. The three types of indoor environments were free of environmental tobacco smoke and gas appliances, as the aim was to asses to what extent PM_2.5, soot and NO₂ infiltrate from outdoors to indoors. The median indoor and outdoor PM_2.5 levels were 8.4 μg m^?3 and 9.3 μg m^?3, respectively. The median indoor levels for soot and NO₂ were 0.66 m^?1 × 10^?5 and 10.0 μg m^?3, respectively. The respective outdoor levels were 0.96 m^?1 × 10^?5 and 12.4 μg m^?3. The median indoor/outdoor (I/O) ratios were 0.93, 0.76 and 0.92 for PM_2.5, soot and NO₂, respectively. Their infiltration factors were influenced by the micro-environment, ventilation type and air exchange rate, with aggregated values of 0.25, 0.55 and 0.64, respectively. Indoor and outdoor NO₂ levels were strongly associated (R² = 0.71), followed by soot (R² = 0.50) and PM_2.5 (R² = 0.16). In Stockholm, the three major indoor environments occupied by children offer little protection against combustion-related particles and gases in the outdoor air. Outdoor PM_2.5 seems to infiltrate less, but indoor sources compensate.     

The chemistry of gaseous acids in medieval churches in Cyprus

Indoor and outdoor concentrations of HCl, HNO₃, HCOOH and CH₃COOH were determined in two medieval churches in Cyprus, during July 2003 and March 2004. The high air exchange rate through the open windows and doors led to lower indoor, compared to outdoor, acid concentrations in July 2003. Indoor pollutant emissions and a low air exchange rate resulted in higher indoor compared to outdoors acid concentrations in both churches during March 2004. Indoor to outdoor inorganic acid ratios were higher than the corresponding indoor to outdoor organic acid ratios during July 2003, whilst the opposite trend was observed during March 2004. Direct acid emission from candle burning appears to play a major role in the observed indoor acid concentrations. Emissions of volatile organic compounds from other sources, like humans, cleaning products and incense, led also to formation or depletion of the gaseous acids via homogeneous photochemical, heterogeneous and dark reaction sequences. Chemical reaction pathways were extensively investigated and appear to explain the observed results. The apparent indoor acid deposition velocities ranged between 0.05 and 0.15 cm s⁻¹.     

Indoor Ozone Exposures

Indoor and outdoor ozone concentrations were measured from late May through October at three office buildings with very different ventilation rates. The indoor values closely tracked the outdoor values, and, depending on the ventilation rate, were 20 to 80 percent of those outdoors. The Indoor/outdoor data are adequately described with a mass balance model. The model can also be coupled with reported air exchange rates to estimate indoor/outdoor ratios for other structures. The results from this and previous studies indicate that Indoor concentrations are frequently a significant fraction of outdoor values. These observations, and the fact that most people spend greater than 90 percent of their time indoors, indicate that indoor ozone exposure (concentration × time) is greater than outdoor exposure for many people. Relatively Inexpensive strategies exist to reduce indoor ozone levels, and these could be implemented to reduce the public’s total ozone exposure.     

A new direct thermal desorption-GC/MS method: Organic speciation of ambient particulate matter collected in Golden, BC

Particulate matter having an aerodynamic diameter less than 2.5 μm (PM2.5) is thought to be implicated in a number of medical conditions, including cancer, rheumatoid arthritis, heart attack, and aging. However, very little chemical speciation data is available for the organic fraction of ambient aerosols. A new direct thermal desorption-gas chromatography/mass spectrometry (TD-GC/MS) method was developed for the analysis of the organic fraction of PM2.5. Samples were collected in Golden, British Columbia, over a 15-month period. n-Alkanes constituted 33–98% by mass of the organic compounds identified. PAHs accounted for 1–65% and biomarkers (hopanes and steranes) 1–8% of the organic mass. Annual mean concentrations were: n-alkanes (0.07–1.55 ng m⁻³), 16 PAHs (0.02–1.83 ng m⁻³), and biomarkers (0.02–0.18 ng m⁻³). Daily levels of these organics were 4.89–74.38 ng m⁻³, 0.27–100.24 ng m⁻³, 0.14–4.39 ng m⁻³, respectively. Ratios of organic carbon to elemental carbon (OC/EC) and trends over time were similar to those observed for PM2.5. There was no clear seasonal variation in the distribution of petroleum biomarkers, but elevated levels of other organic species were observed during the winter. Strong correlations between PAHs and EC, and between petroleum biomarkers and EC, suggest a common emission source – most likely motor vehicles and space heating.     

Atmospheric mercury cycles in northern Wisconsin

Total gaseous mercury (TGM) in the lower atmosphere of northern Wisconsin exhibits strong annual and diurnal cycles similar to those previously reported for other rural monitoring sites across mid-latitude North America. Annually, TGM was highest in late winter and then gradually declined until late summer. During 2002–04, the average TGM concentration was 1.4 ± 0.2 (SD) ng m^?3, and the amplitude of the annual cycle was 0.4 ng m^?3 (～30% of the long-term mean). The diurnal cycle was characterized by increasing TGM concentrations during the morning followed by decreases during the afternoon and night. The diurnal amplitude was variable but it was largest in spring and summer, when daily TGM oscillations of 20–40% were not uncommon. Notably, we also observed a diurnal cycle for TGM indoors in a room ventilated through an open window. Even though TGM concentrations were an order of magnitude higher indoors, (presumably due to historical practices within the building: e.g. latex paint, fluorescent lamps, thermometers), the diurnal cycle was remarkably similar to that observed outdoors. The indoor cycle was not directly attributable to human activity, the metabolic activity of vegetation or diurnal atmospheric dynamics; but it was related to changes in temperature and oxidants in outdoor air that infiltrated the room. Although there was an obvious difference in the proximal source of indoor and outdoor TGM, similarities in behavior suggest that common TGM cycles may be driven largely by adsorption/desorption reactions involving solid surfaces, such as leaves, snow, dust and walls. Such behavior would imply a short residence time for Hg in the lower atmosphere and intense recycling – consistent with the “ping-pong ball” or “multi-hop” conceptual models proposed by others.     

Indoor and outdoor air quality investigation at schools in Hong Kong

Five classrooms in Hong Kong (HK), air-conditioned or ceiling fans ventilated, were chosen for investigation of indoor and outdoor air quality. Parameters such as temperature, relative humidity (RH), carbon dioxide (CO2), sulphur dioxide (SO2), nitric oxide (NO), nitrogen dioxide (NO2), respirable particulate matter (PM10), formaldehyde (HCHO), and total bacteria counts were monitored indoors and outdoors simultaneously. The average respirable particulate matter concentrations were higher than the HK Objective, and the maximum indoor PM10 level exceeded 1000 microg/m3. Indoor CO2 concentrations often exceeded 1000 microl/l in air-conditioning and ceiling fan classrooms, indicating inadequate ventilation. Maximum indoor CO2 level reached 5900 microl/l during class at the classroom with cooling tower ventilation. Increasing the rate of ventilation or implementation of breaks between classes is recommended to alleviate the high CO2 level. Other pollution parameters measured in this study complied with the standards. The two most important classroom air quality problems in Hong Kong were PM10 and CO2 levels.     

Vertical distribution of polycyclic aromatic hydrocarbons in atmospheric boundary layer of Beijing in winter

Air samples were collected using active samplers at various heights of 8, 15, 32, 47, 65, 80, 102, 120, 140, 160, 180, 200, 240, 280 and 320 m on a meteorological tower in an urban area of Beijing in two campaigns in winter 2006. Altitudinal distributions of polycyclic aromatic hydrocarbons (PAHs) in atmospheric boundary layer of Beijing in winter season were investigated. Meteorological conditions during the studied period were characterized by online measurements of four meteorological parameters as well as trajectory calculation. The mean total concentrations of 15 PAHs except naphthalene of gaseous and particulate phase were 667±450 and 331±144 ng m⁻³ in January and 61±19 and 29±6 ng m⁻³ in March, respectively. Domestic coal combustion and vehicle emission were the dominant PAH sources in winter. Although the composition profiles derived from the two campaigns were similar, the concentrations were different by one order of magnitude. The higher concentrations in January were partly caused by higher emission due to colder weather than March. Moreover, weak wind, passing through the city center before the sampling site, picked up more contaminants on the way and provided unfavorable dispersion condition in January. For both campaigns, PAH concentrations decreased with heights because of ground-level emission and unfavorable dispersion conditions in winter. The concentration ratio of PAHs in gas versus solid phases was temperature dependent and negatively correlated to their octanol–air partition coefficients.     

A new detailed chemical model for indoor air pollution

A detailed chemical box model has been constructed based on a comprehensive chemical mechanism (the Master Chemical Mechanism) to investigate indoor air chemistry in a typical urban residence in the UK. Unlike previous modelling studies of indoor air chemistry, the mechanism adopted contains no simplifications such as lumping or the use of surrogate species, allowing more insight into indoor air chemistry than previously possible. The chemical mechanism, which has been modified to include the degradation reactions of key indoor air pollutants, contains around 15,400 reactions and 4700 species. The results show a predicted indoor OH radical concentration up to 4.0×10⁵ molecule cm⁻³, only a factor of 10–20 less than typically observed outdoors and sufficient for significant chemical cycling to take place. Concentrations of PAN-type species and organic nitrates are found to be important indoors, reaching concentrations of a few ppb. Sensitivity tests highlight that the most crucial parameters for modelling the concentration of OH are the light-intensity levels and the air exchange rate. Outdoor concentrations of O₃ and NO_X are also important in determining radical concentrations indoors. The reactions of ozone with alkenes and monoterpenes play a major role in producing new radicals, unlike outdoors where photolysis reactions are pivotal radical initiators. In terms of radical propagation, the reaction of HO₂ with NO has the most profound influence on OH concentrations indoors. Cycling between OH and RO₂ is dominated by reaction with the monoterpene species, whilst alcohols play a major role in converting OH to HO₂. Surprisingly, the absolute reaction rates are similar to those observed outdoors in a suburban environment in the UK during the summer. The results from this study highlight the importance of tailoring a model for its particular location and the need for future indoor air measurements of radical species, nitrated species such as PANs and organic nitrates, photolysis rates of key species over the range of wavelengths observed indoors and concurrent measurements of outdoor air pollutant concentrations.     

Altitude dependence of polychlorinated biphenyls (PCBs) and polybrominated diphenyl ethers (PBDEs) in surface soil from Tibetan Plateau, China

Remote mountain areas besides high latitude regions are beginning to receive increased attention in studying the transport and behavior of persistent organic pollutants (POPs). In the present work, surface soil samples were collected from the Tibetan Plateau, the highest plateau in the world which includes the northern slope of Mt. Qomolangma, to investigate the levels and trends of polychlorinated biphenyls (PCBs) and polybrominated diphenyl ethers (PBDEs) along the altitudinal gradient. The average PCB and PBDE concentrations were 185.6 ng kg⁻¹ dry weight (dw) (range 47.1–422.6 ng kg⁻¹ dw) and 11.1 ng kg⁻¹ dw (range 4.3–34.9 ng kg⁻¹ dw), respectively. Regression analysis between the log-transformed TOC-normalized concentrations and the altitudes of the sampling sites showed two opposite trends with regard to altitude dependence: negative relationship with altitude below about 4500 m followed by a positive altitude dependence above this point. Considering minimum anthropogenic activities and very sparse precipitation in the north of Himalayas, the trends above 4500 m imply that the significant altitude dependence of these two groups of POPs were irrespective of pollution sources, but could be predicted by the global distillation effect involving cold condensation in high altitude mountain areas. Increasing levels of heavier congeners were found in higher altitude sites, although the lighter congeners were the main contributors to the total amount, suggesting that less volatile congeners seem to become enriched easier than those more volatile at higher altitudes in this region.     

Air Pollution In Pittsburgh: A Historical Perspective

Sources and concentrations of indoor air pollutants and aeroallergens were evaluated in the arid Southwest community of Tucson, Arizona. One major purpose was to appraise the interaction of indoor and outdoor human exposures. A rough time budget study showed that 74% of adults spent 75% or more of their time in some indoor environment. Outdoor and indoor concentrations of TSP, RSP, CO, O₃ and aeroallergens were measured for 41 detached dwellings. Small area and basin monitoring occurred for TSP, CO, NO₂, O₃ and aeroallergens; ambient TSP frequently exceeds NAAQS and both CO and O3 do occasionally. Indoor TSP and RSP were lower than outdoors and were of a different composition. Outdoor infiltration falls rapidly for particles and pollen, related to distance Indoors. CO was low and O₃ was very low indoors. TSP and RSP correlated significantly with tobacco smoking and CO correlated with gas stove usage. Temperature varied minimally indoors and relative humidity indoors was similar to outdoor readings In this climate. It was concluded that better particle characterization and better estimates of total exposure are required.     

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.     

Characteristics of Indoor Aerosols in Residential Homes in Urban Locations: A Case Study in Singapore

Abstract

As part of a major study to investigate the indoor air quality in residential houses in Singapore, intensive aerosol measurements were made in an apartment in a multistory building for several consecutive days in 2004. The purpose of this work was to identify the major indoor sources of fine airborne particles and to assess their impact on indoor air quality for a typical residential home in an urban area in a densely populated country. Particle number and mass concentrations were measured in three rooms of the home using a real-time particle counter and a low-volume particulate sampler, respectively. Particle number concentrations were found to be elevated on several occasions during the measurements. All of the events of elevated particle concentrations were linked to indoor activities based on house occupant log entries. This enabled identification of the indoor sources that contributed to indoor particle concentrations. Activities such as cooking elevated particle number concentrations ≤2.05 × 10⁵ particles/cm³. The fine particles collected on Teflon filter substrates were analyzed for selected ions, trace elements, and metals, as well as elemental and organic carbon (OC) contents. To compare the quality of air between the indoors of the home and the outdoors, measurements were also made outside the home to obtain outdoor samples. The chemical composition of both outdoor and indoor particles was determined. Indoor/outdoor (I/O) ratios suggest that certain chemical constituents of indoor particles, such as chloride, sodium, aluminum, cobalt, copper, iron, manganese, titanium, vanadium, zinc, and elemental carbon, were derived through migration of outdoor particles (I/O<1 or ≈1), whereas the levels of others, such as nitrite, nitrate, sul-fate, ammonium, cadmium, chromium, nickel, lead, and OC, were largely influenced by the presence of indoor sources (I/O >1).     

Effect of outside air ventilation rate on volatile organic compound concentrations in a call center

A study of the relationship between outside air ventilation rate and concentrations of volatile organic compounds (VOCs) generated indoors was conducted in a call center office building. The building, with two floors and a total floor area of 4600 m², is located in the San Francisco Bay Area, CA. Ventilation rates were manipulated with the building's four air handling units (AHUs). VOC and CO₂ concentrations in the AHU returns were measured on 7 days during a 13-week period. VOC emission factors were determined for individual zones on days when they were operating at near steady-state conditions. The emission factor data were subjected to principal component (PC) analysis to identify groups of co-varying compounds. Potential sources of the PC vectors were ascribed based on information from the literature. The per occupant CO₂ generation rates were 0.0068–0.0092 l s⁻¹. The per occupant isoprene generation rates of 0.2–0.3 mg h⁻¹ were consistent with the value predicted by mass balance from breath concentration and exhalation rate. The relationships between indoor minus outdoor VOC concentrations and ventilation rate were qualitatively examined for eight VOCs. Of these, acetaldehyde and hexanal, which likely were associated with material sources, and decamethylcyclopentasiloxane, associated with personal care products, exhibited general trends of higher concentrations at lower ventilation rates. For other compounds, a clear inverse relationship between VOC concentrations and ventilation was not observed. The net concentration of 2,2,4-trimethyl-1,3-pentanediol monoisobutyrate isomers, examples of low-volatility compounds, changed very little with ventilation likely due to sorption and re-emission effects. These results illustrate that the efficacy of ventilation for controlling VOC concentrations can vary considerably depending upon the operation of the building, the pollutant sources and the physical and chemical processes affecting the pollutants. Thus, source control measures, in addition to adequate ventilation, are required to limit concentrations of VOCs in office buildings.     

Comparative study on indoor air quality in Japan and China: Characteristics of residential indoor and outdoor VOCs

We conducted a comparative study on the indoor air quality for Japan and China to investigate aromatic volatile organic compounds (VOCs) in indoor microenvironments (living room, bedroom, and kitchen) and outdoors in summer and winter during 2006–2007. Samples were taken from Shizuoka in Japan and Hangzhou in China, which are urban cities with similar latitudes. Throughout the samplings, the indoor and outdoor concentrations of many of the targeted VOCs (benzene, toluene, ethylbenzene, xylenes, and trimethylbenzenes) in China were significantly higher than those in Japan. The indoor concentrations of VOCs in Japan were somewhat consistent with those outdoors, whereas those in China tended to be higher than those outdoors. Here, we investigated the differences in VOC concentrations between Japan and China. Compositional analysis of indoor and outdoor VOCs showed bilateral differences; the contribution of benzene in China was remarkably higher than that in Japan. Significant correlations (p < 0.05) for benzene were observed among the concentrations in indoor microenvironments and between the outdoors and living rooms or kitchens in Japan. In China, however, significant correlations were observed only between living rooms and bedrooms. These findings suggest differences in strengths of indoor VOC emissions between Japan and China. The source characterizations were also investigated using principal component analysis/absolute principal component scores. It was found that outdoor sources including vehicle emission and industrial sources, and human activity could be significant sources of indoor VOC pollution in Japan and China respectively. In addition, the lifetime cancer risks estimated from unit risks and geometric mean indoor concentrations of carcinogenic VOCs were 2.3 × 10^?5 in Japan and 21 × 10^?5 in China, indicating that the exposure risks in China were approximately 10 times higher than those in Japan.     

Occurrence and possible sources of polychlorinated biphenyls in surface sediments from the Wuhan reach of the Yangtze River, China

Twenty-seven surface sediment samples were collected from the mainstream and eight tributaries of the Wuhan reach of the Yangtze River, China, in 2005, in order to assess the distribution, possible sources, and potential risk of polychlorinated biphenyls (PCBs) in the environment. The total concentrations of PCBs (the sum of 39 congeners) ranged from 1.2 to 45.1 ng g⁻¹ dry weight, with a mean value of 9.2 ng g⁻¹. Sediment samples with the highest PCB concentrations came from the tributary sites, which are closer to PCB sources. Conversely, PCB concentrations in the sediment from the mainstream sites of Yangtze River were relatively low. The observed PCB levels were higher than those found in the sediments of other rivers in China, but lower than those in river sediments from other urban areas and harbors around the world. Low-chlorinated PCBs, dominated by tetra-PCBs and penta-PCBs, were identified as being prevalent in the surface sediments. Correlation analyses between the PCBs and the geochemistry and heavy metal content of the sediments suggest that the washing of these compounds from the land into the river by floods and heavy rains, or industrial wastewater and domestic sewage, may be the major sources of the PCBs. According to established sediment quality guidelines, the risk of adverse biological effects from the levels of PCBs recorded at most of the studied sites should be insignificant, although the higher concentrations at other sites could cause acute biological damage.     

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.     

Spatial character of polychlorinated biphenyls from soil and respirable particulate matter in Taiyuan, China

As one of China’s great metropolises, Taiyuan is affected by heavy chemical industry and manufacture of chemical products, and faces pollution from polychlorinated biphenyls (PCBs). Therefore, this study was conducted to determine the PCB concentrations in various environmental media in Taiyuan. We collected 15 soil samples, 34 respirable particulate matter (PM) samples (17 of PM_2.5 and 17 of PM₁₀) from urban areas of Taiyuan, and measured a total of 144 PCB congeners (including some coeluting PCB congeners). The total PCB concentrations were 51–4.7 × 10³ pg g⁻¹ in soil, 27–1.4 × 10² pg m⁻³ in PM_2.5 and 16–1.9 × 10² pg m⁻³ in PM₁₀. Of the PCB homologues, the dominant PCBs detected in the various media were all tri-CBs. Soil was relatively the most polluted media. Furthermore, principal-component analysis revealed that the major PCB source in Taiyuan may be associated with the main commercial PCB through long-range transmission. Toxic equivalency (TEQ) concentrations (based on ten dioxin-like PCBs) ranged from N.D. to 5.9 × 10⁻³ pg-WHO TEQ g⁻¹ in soil, 2.0 × 10⁻⁴–3.4 × 10⁻³ pg-WHO TEQ m⁻³ and 1.0 × 10⁻⁴–1.2 × 10⁻³ pg-WHO TEQ m⁻³ in PM_2.5 and PM₁₀, respectively. In previous studies, PCBs were not a severe component of contaminant in Taiyuan; however, this study suggested there is a potential threat of human exposure to PCBs for residents of Taiyuan.     

Year-long continuous personal exposure to PM2.5 recorded by a fast responding portable nephelometer

Personal exposure to particulate matter of aerodynamic diameter under 2.5 μm (PM_2.5) was monitored using a DustTrak nephelometer. The battery-operated unit, worn by an adult individual for a period of approximately one year, logged integrated average PM_2.5 concentrations over 5 min intervals. A detailed time-activity diary was used to record the experimental subject’s movement and the microenvironments visited. Altogether 239 days covering all the months (except April) were available for the analysis. In total, 60 463 acceptable 5-min averages were obtained. The dataset was divided into 7 indoor and 4 outdoor microenvironments. Of the total time, 84% was spent indoors, 10.9% outdoors and 5.1% in transport. The indoor 5-min PM_2.5 average was higher (55.7 μg m^?3) than the outdoor value (49.8 μg m^?3). The highest 5-min PM_2.5 average concentration was detected in restaurant microenvironments (1103 μg m^?3), the second highest 5-min average concentration was recorded in indoor spaces heated by stoves burning solid fuels (420 μg m^?3). The lowest 5-min mean aerosol concentrations were detected outdoors in rural/natural environments (25 μg m^?3) and indoors at the monitored person’s home (36 μg m^?3). Outdoor and indoor concentrations of PM_2.5 measured by the nephelometer at home and during movement in the vicinity of the experimental subject’s home were compared with those of the nearest fixed-site monitor of the national air quality monitoring network. The high correlation coefficient (0.78) between the personal and fixed-site monitor aerosol concentrations suggested that fixed-site monitor data can be used as proxies for personal exposure in residential and some other microenvironments. Collocated measurements with a reference method (β-attenuation) showed a non-linear systematic bias of the light-scattering method, limiting the use of direct concentration readings for exact exposure analysis.