Total Particle-bound Polycyclic Aromatic Hydrocarbons Research Articles

Characteristics of particle-bound polycyclic aromatic hydrocarbons (PAHs) in indoor PM2.5 of households in the Southwest part of Ulaanbaatar capital, Mongolia

Air pollution, including PM2.5 concentration in Ulaanbaatar (capital of Mongolia) is a serious matter of concern. As the majority of households use coal in large areas of the city, indoor air quality is also posing a serious risk to human health. This study investigated the concentration of polycyclic aromatic compounds (PAHs) in indoor particulate matter (PM2.5) in 10 non-smoker households. Sampling was conducted in winter of 2018, between 27 January and 09 February. Concentrations of PM2.5 in the indoor air of households ranged between 62.8 and 324.8 µg m−3. Total concentration of PAHs also varied in a relatively wide range, between 46.2 and 175.7 ng m−3. Five-ring PAHs represented a considerably high fraction of total PAHs between 25 and 53%, benzo[b]fluoranthene (BbF) and benzo[a]pyrene (BaP) were the two predominant compounds within five-ring PAHs. Significant correlation was found between indoor and outdoor particulate matter levels in wintertime. Considering individual characteristic PAHs, heavier PAHs homologues (4- to 5-ring and 6-ring PAHs) were detected in all households, which suggested the influence of coal combustion and traffic exhaust. Health risk of children attributed to PAHs inhalation was assessed by taking into account the lifetime-average daily dose (LADD) and corresponding lifetime cancer risk. Lifetime average daily dose for children in only one household were slightly higher than health-based guideline level (1.0 × 10−5), defined by WHO, whereas LADD for adults and children of other households were within acceptable limit. The cancer risks from the exposure of children to air pollutants in all households except HH-3 were found high. In the Vibrio fischeri bioluminescence inhibition assay, according to the toxic unit (TU) values of indoor PM2.5 from ten households, all samples were classified as toxic.

Particle-bound PAHs induced glucose metabolism disorders through HIF-1 pathway

Vehicle exhaust, as one of the most important compositions of air pollution, induced various adverse health effects, especially diabetes, on human beings. Even though monitoring and epidemiological data indicates that particle-bound polycyclic aromatic hydrocarbons (PAHs) is an inducing factor of diabetes, the specific causative mechanisms are still unclear. In the current study, the concentration of particulate matters (PMs, including PM1.0, PM2.5 and PM10.0) and PAHs was investigated at rush hour of weekday in three urban underground parking garages (UPGs). To evaluate the impacts of particle-bound PAHs on human beings, analysis of non-target metabolomics and unmetabolized PAHs were conducted for UPG and non-UPG worker urine samples. The results showed that the highest concentrations of PMs and total PAHs were found at the UPG entrance. The concentrations of unmetabolized 5-6 rings PAHs in the UPG worker urine were significantly higher than that in non-UPG worker urine samples, which induced glucose metabolism disorders through hypoxia-inducible factor 1 (HIF-1) signaling pathway. This could be a reason for particle-bound PAHs induced-diabetes on road workers, drivers and garage staff. These findings can serve as a step towards air pollution management and the pathological mechanism analysis of environmental factor induced-diseases.

Total p-PAH Levels Nearby a Complex Industrial Area: A Tailored Monitoring Experiment to Assess the Impact of Emission Sources

In this study, data on the hourly concentrations of the total particle-bound Polycyclic Aromatic Hydrocarbons (p-PAHs) collected between 1 August 2013 and 31 August 2014 by the air quality fence monitoring network of the biggest European steel plant, were analyzed. In contrast with what was predicted, the total p-PAH concentration did not decrease with distance from the steel plant, and higher concentrations were registered at the Orsini site, in the urban settlement, relative to the Parchi site, which is nearest to the coke ovens. Therefore, in order to identify and explain the cause of these high concentrations, a tailored monitoring experiment was carried out on a specific monitoring pathway by using a total p-PAHs monitor placed onto a cart. The real-time monitoring of the total p-PAH concentration on the road revealed to be a useful tool, which identified vehicular traffic as an important source of p-PAHs and highlighted the possible high short-term effect that vehicular traffic sources could have on the health of the exposed human population. Moreover, the study focused attention on the importance of the spatial representativeness of fixed monitoring stations, especially in a highly complex industrial area such as Taranto (Southern Italy).

Experimental Study of Particulate Emission Characteristics from A Gasoline Direct Injection Engine During Starting Process

The engine starting process presents high particulate emissions in exhaust. This study gives a systematic investigation on particulate emission characteristics, including particulate matter (PM) mass, soluble organic fraction (SOF) mass, C10-C26 n-Alkanes and particle-bound polycyclic aromatic hydrocarbons (PAHs), that have been emitted from a gasoline direct injection (GDI) engine measured by Gas chromatography-mass spectrometry during starting period. The results show that particulate emissions under the warm coolant start condition decline dramatically compared with the cold start condition. 90 % of particulate number (PN) emitted during the cold and warm start periods generally are nucleation-mode particles. Over 50 % PM mass and PAHs emissions are emitted in the first 0–13 s stage. SOF mass accounts more than 60 % in PM mass emissions, especially under the warm coolant start condition. Some C23–C26 n-Alkanes are detected under the cold start condition which demonstrates that partial particulate composition directly comes from lubricant. The concentration of the two ring PAHs is the lowest among PAHs while the four to six ring PAHs are higher under the cold start operation. The toxicity of PAHs which is evaluated by Benzo(a)pyrene equivalent toxicity (BEQ) value of the total PAHs emissions shows a decline of 66.83 % under the warm start condition.

Fine particle-bound polycyclic aromatic hydrocarbons (PAHs) at an urban site of Wuhan, central China: Characteristics, potential sources and cancer risks apportionment

Levels, compositions, sources, and cancer risks of fine particle (PM2.5)-bound PAHs were investigated at an urban site of Wuhan, Central China. Totally 115 PM2.5 samples collected during four seasons from 2014 to 2015 were analyzed for 16 USEPA priority PAHs. The annual average of PM2.5 and total PAHs were 106 ± 41.7 μg m−3 and 25.1 ± 19.4 ng m−3, respectively. The seasonal levels of PM2.5 and PAHs varied in a similar trend, with the highest concentrations in winter and the lowest in summer. PM2.5-bound PAHs under different pollution level was discussed and the highest average PAH levels were found at a moderate (115–150 μg m−3) air quality level. Three sources including coal combustion and biomass burning, petrogenic source, and vehicle emissions were extracted and quantified by the positive matrix factorization (PMF) model, accounting for 22.7 ± 21.3%, 34.4 ± 29.0% and 42.9 ± 31.3% of the total PAHs, respectively. The potential source contribution function (PSCF) and the concentration-weighted trajectory (CWT) were combined to explore the geographic origins of PAHs. The spatial distributions of coal combustion and biomass burning, petrogenic source, and vehicle emissions were well correlated with medium molecular weight (MMW), low molecular weight (LMW) and high molecular weight (HMW) PAHs, respectively. Results of PSCF and CWT indicated that the long-distance transport form north of Wuhan as far as northern and eastern of China was higher than that from the southern China while the contribution of local areas was higher than those from the long-range transport. The overall lifetime lung cancer risk (LLCR) via inhalation exposure to PM2.5-bound PAHs was estimated as 3.03 × 10−4, with vehicle emissions contributed 57.1% (1.6 × 10−4) to the total risk on average, followed by coal combustion and biomass burning (31.0%, 9.6 × 10−5), and petrogenic source (11.9%, 3.6 × 10−5).

Local and seasonal variations in concentrations of chlorinated polycyclic aromatic hydrocarbons associated with particles in a Japanese megacity

Concentrations of particle-bound polycyclic aromatic hydrocarbons (PAHs) and chlorinated PAHs (ClPAHs) were measured in different seasons at five sampling stations in Nagoya, a Japanese megacity. The annual mean total ClPAH and total PAH concentrations were 43.3–92.6pg/m3 and 5200–8570pg/m3, respectively. The concentrations of total ClPAHs were significantly variable than those of total PAHs, and both total concentrations through the seasons did not significantly correlate at any of the stations. Principal component analysis was used to characterize the ClPAH sources, resulted that ClPAHs were found to be associated with the sources of high-molecular-weight PAHs in the warmer seasons and of low-molecular-weight PAHs in the colder seasons. These findings suggest that principal sources of particle-bound ClPAHs are present in the local area, and change in the seasons. Toxic equivalent (TEQ) concentrations were estimated to assess the risks associated with exposure to ClPAHs in air. The TEQ concentrations in the samples were 0.05–0.32pg-TEQ/m3. The TEQ concentrations in summer were approximately half the TEQ concentrations in the other seasons at all of the stations.

Characteristics and sources of polycyclic aromatic hydrocarbons in atmospheric aerosols in the Kathmandu Valley, Nepal

The Kathmandu Valley in the foothills of the Himalayas, where the capital city of Nepal is located, has one of the most serious air pollution problems in the world. In this study, total suspended particle (TSP) samples collected over a year (April 2013–March 2014) in the Kathmandu Valley were analyzed for determining the concentrations of 15 priority particle-bound polycyclic aromatic hydrocarbons (PAHs). The TSP and PAH concentrations were extremely high, with annual average concentration being 199±124μg/m3 and 155±130ng/m3, respectively, which are comparable to those observed in Asian cities such as Beijing and Delhi. The TSP and PAH concentrations varied considerably, with the seasonal average concentration being maximal during the post-monsoon season followed by, in descending order, the winter, pre-monsoon, and monsoon seasons. In the winter and pre-monsoon seasons, ambient TSP and PAH concentrations increased because of emissions from brick kilns and the use of numerous small generators. Moreover, in the pre-monsoon season, forest fires in the surrounding regions influenced the TSP and PAH concentrations in the valley. PAHs with 4 to 6 rings constituted a predominant proportion (92.3–93.3%) of the total PAHs throughout the year. Evaluation of diagnostic molecular ratios indicated that the atmospheric PAHs in the Kathmandu Valley originated mainly from diesel and biomass combustion. The toxic equivalent quantity (TEQ) of particle phase PAHs ranged between 2.74 and 81.5ngTEQ/m3, which is considerably higher than those reported in other South Asian cities, and 2–80 times higher than the World Health Organization guideline (1ngTEQ/m3). This suggests that ambient PAH levels in the Kathmandu Valley pose a serious health risk to its approximately 3.5 million residents.

Indoor emission, dispersion and exposure of total particle-bound polycyclic aromatic hydrocarbons during cooking

Cooking processes highly contribute to indoor polycyclic aromatic hydrocarbon (PAH) pollution. High molecular weight and potentially carcinogenic PAHs are generally found attached to small particles, i.e., particulate phase PAHs (PPAHs). Due to the fact that indoor particle dynamics have been clear, describing the indoor dynamics of cooking-generated PPAHs within a specific time span is possible. This paper attempted to quantify the dynamic emission rate, simultaneous spatial dispersion and individual exposure of PPAHs using a cooking source. Experiments were conducted in a real-scale kitchen chamber to elucidate the time-resolved emission and effect of edible oil temperature and mass. Numerical simulations based on indoor particle dynamics were performed to obtain the spatial dispersion and individual inhalation intake of PPAHs under different emission and ventilation conditions. The present work examined the preheating cooking stage, at which edible oil is heated up to beyond its smoke point. The dynamic emission rate peak point occurred much earlier than the oil heating temperature. The total PPAH emission ranged from 2258 to 6578 ng upon heating 40–85 g of edible oil. The overall intake fraction by an individual within a period of 10 min, including 3 min for heating and 7 min for natural cooling, was generally ∼1/10,000. An important outcome of this work was that the overall intake fraction could be represented by multiplying the range hood escape efficiency by the inhalation-to-ventilation rate ratio, which would be no greater than the same ratio. The methodology and results of this work were extendible for the number-based assessment of PPAHs. This work is expected to help us understand the health risks due to inhalation exposure to cooking-generated PPAHs in the kitchen.

Variation in PAH patterns in road runoff

Twelve particle-bound polycyclic aromatic hydrocarbons (PAHs) were measured in the first flush regime of road runoff during nine events in Winterthur in Switzerland. The total PAH contents ranged from 17 to 62 μg/g. The PAH patterns measured at different time intervals during the first flush periods were very similar within each event irrespective of variation in suspended solids (SS) concentration within the first flush regime. However, the PAH patterns were different from event to event. This indicates that the environment plays an important role in PAH accumulation in SS. A toxicity identification evaluation approach using a toxicity equivalency factor (TEF) was applied to compare toxicities in the different events. The TEFs were found to be between 8 and 33 μg TEQ g(-1) (TEQ: toxic equivalent concentration). In some cases, two events having similar total PAH contents showed two fold toxicity differences.

Emission and size distribution of particle-bound polycyclic aromatic hydrocarbons from residential wood combustion in rural China

Emissions and size distributions of 28 particle-bound polycyclic aromatic hydrocarbons (PAHs) from residential combustion of 19 fuels in a domestic cooking stove in rural China were studied. Measured emission factors of total particle-bound PAHs were 1.79 ± 1.55, 12.1 ± 9.1, and 5.36 ± 4.46 mg kg−1 for fuel wood, brushwood, and bamboo, respectively. Approximate 86.7, 65.0, and 79.7% of the PAHs were associated with fine particulate matter with size less than 2.1 μm for these three types of fuels, respectively. Statistically significant differences in emission factors and size distributions of particle-bound PAHs between fuel wood and brushwood were observed, with the former had lower emission factors but more PAHs in finer PM. Mass fraction of the fine particles associated PAHs was found to be positively correlated with fuel density and moisture, and negatively correlated with combustion efficiency. Low and high molecular weight PAHs preferably segregated into the coarse and fine PM, respectively. The high accumulation tendency of the PAHs from residential wood combustion in fine particles implies strong adverse health impact.

Characteristics of nano-/ultrafine particle-bound PAHs in ambient air at an international airport

Concentrations of 22 polycyclic aromatic hydrocarbons (PAHs) were estimated for individual particle-size distributions at the airport apron of the Taipei International Airport, Taiwan, on 48 days in July, September, October, and December of 2011. In total, 672 integrated air samples were collected using a micro-orifice uniform deposition impactor (MOUDI) and a nano-MOUDI. Particle-bound PAHs (P-PAHs) were analyzed by gas chromatography with mass selective detector (GC/MSD). The five most abundant species of P-PAHs on all sampling days were naphthalene (NaP), phenanthrene (PA), fluoranthene (FL), acenaphthene (AcP), and pyrene (Pyr). Total P-PAHs concentrations were 152.21, 184.83, and 188.94 ng/m(3) in summer, autumn, and winter, respectively. On average, the most abundant fractions of benzo[a]pyrene equivalent concentration (BaPeq) in different molecular weights were high-weight PAHs (79.29 %), followed by medium-weight PAHs (11.57 %) and low-weight PAHs (9.14 %). The mean BaPeq concentrations were 1.25 and 0.94 (ng/m(3)) in ultrafine particles (<0.1 μm) and nano-particles (<0.032 μm), respectively. The percentages of total BaPeq in nano- and ultrafine particulate size ranges were 52.4 % and 70.15 %, respectively.

Composition and comparative toxicity of particulate matter emitted from a diesel and biodiesel fuelled CRDI engine

Abstract There is a global concern about adverse health effects of particulate matter (PM) originating from diesel engine exhaust. In the current study, parametric investigations were carried out using a CRDI (Common Rail Direct Injection) diesel engine operated at different loads at two different engine speeds (1800 and 2400 rpm), employing diesel and 20% biodiesel blends (B20) produced from Karanja oil. A partial flow dilution tunnel was employed to collect and measure the mass of the primary particulates from diesel and biodiesel blend collected on a 47 mm quartz substrate. The collected PM (particulate matter) was subjected to chemical analyses in order to assess the amount of Benzene Soluble Organic Fraction (BSOF) and trace metals using Inductively Coupled Plasma-Optical Emission Spectrometer (ICP-OES). For both diesel and biodiesel, BSOF results showed decreasing levels with increasing engine load. B20 showed higher BSOF as compared to those measured with diesel. The concentration of different trace metals analyzed also showed decreasing trends with increasing engine loads. In addition, real-time measurements for Organic Carbon (OC), Elemental Carbon (EC) and total particle-bound Polycyclic Aromatic Hydrocarbons (PAHs) were carried out on the primary engine exhaust coming out of the partial flow dilution tunnel. Analysis of OC/EC data suggested that the ratio of OC to EC decreases with corresponding increase in engine load for both fuels. A peak in PAH concentration was observed at 60% engine load at 1800 rpm and 20% engine load at 2400 rpm engine speeds almost identical for both kinds of fuels. Comparison of chemical components of PM emitted from this CRDI engine provides new insight in terms of PM toxicity for B20 vis-a-vis diesel.

Sizes and polycyclic aromatic hydrocarbon composition distributions of nano, ultrafine, fine, and coarse particulates emitted from a four-stroke motorcycle

Thus, this study was undertaken to determine the size distribution, concentration, species, and carcinogenic potency of particulate matter and particle-bound polycyclic aromatic hydrocarbons (PAHs) emitted from 4-st/mc at various speeds (idle, 15 km/h, 30 km/h). Approximately 80% of the particles emitted from the that is, they are primary inhalable particulates. The particle total number concentrations (TNCs) emitted while idling and at 15 and 30 km/h were 2.07 × 104, 2.35 × 104, and 2.60 × 104 #/cm3, respectively; i.e., they increased at elevated speeds. Notably, most of the particles emitted at 30 km/h had diameters of less than 0.65 μm and contained higher percentages of total PAHs. Excluding incomplete combustion, we suspected that some of the lower-molecular-weight PAHs [phenanthrene (PA), anthracene (Ant), pyrene (Pyr)] obtained in the fine particles at idle originated from unburned 95-octane unleaded fuel. When operated at 15 km/h, pyrolysis of the PAHs dominated, resulting in increased amounts of medium-molecular-weight PAHs {fluorene (FL), Pyr, benz[a]anthracene (BaA), chrysene (CHR)} in the ultrafine particles. Furthermore, at 30 km/h, more pyrosynthesis products {benzo[a]pyrene (BaP), indeno[1,2,3,-cd]pyrene (IND), dibenz[a,h]anthracene (DBA)}, induced through combustion at the correspondingly higher temperature, were exhausted with the nanoparticles. Although the total concentrations of BaP-equivalent emissions were inconsistent with the total PAHs, the nanoscale-sized particulates emitted from the 4-st/mc at higher speeds had the strongest PAH-related carcinogenic potencies, which should be a great concern.

The effect of EURO-0 vehicle substitution on polycyclic aromatic hydrocarbon and carbon monoxide concentrations in an urban area

From 1994 to 2003, daily air concentrations of particle-bound polycyclic aromatic hydrocarbons (PAHs) and carbon monoxide (CO) were regularly monitored at two traffic-oriented sampling sites (A and B) in urban Genoa, Italy. The data were used to estimate effects on air quality in real situations due to progressive substitution of EURO-0 vehicles, started in 1993, with less-polluting vehicles (EURO-1, EURO-2), mainly gasoline vehicles with a catalyst. PAH profile classification and diagnostic PAH ratios were used to identify 345 samples of predominantly traffic origin. At both sites, CO and PAH daily concentrations decreased exponentially with time and the apparent half-life values calculated were 6.3 and 5.5 for CO and 3.7 and 3.5 years for PAHs at sites A and B, respectively. At site A, monitored for traffic intensity, multiple regression analyses confirmed that daily PAH and CO concentrations were positively correlated with the number of non-catalytic vehicles estimated to cross this site during sampling and negatively correlated with seasonal variables (air temperature, ozone concentration, relative air humidity). The reduction in air pollution estimated for complete substitution of non-catalytic gasoline vehicles was 89% for BaP, 85% for total PAHs and 69% for CO.

Identification of Surrogate Measures of Diesel Exhaust Exposure in a Controlled Chamber Study

Exposure to diesel exhaust (DE) has been associated with acute cardiopulmonary and vascular responses, chronic noncancer health effects, and respiratory cancers in humans. To better understand DE exposures and eventually their related health effects, we established a controlled chamber experiment wherein human volunteer subjects were exposed to approximately 100 microg/m3 DE. In general, human exposure assessment for DE is based on ambient air measurements of surrogates such as elemental carbon (EC) or total organic carbon (OC) collected on filters. As specific health effect mechanisms and dose-response are obscured bythe complex composition of DE, the linkage from exposure to internal dose can presumably be improved by use of specific biomarkers and metabolites in blood, breath, or urine. Because EC and OC are not suitable as biomarkers, in this study, we focus on identifying compounds that are demonstrated indicators of DE and can also be found in biological fluids. We measured an assortment of volatile, semivolatile, and particle-bound aromatic compounds in the chamber air and report their airborne concentrations in DE and purified air, as well as the estimated values of the corresponding exposure ratios (mean DE air concentration:mean purified air concentration). These estimated exposure ratios were used to identify naphthalene (Nap) and phenanthrene (Phe) as potentially useful surrogates for DE exposure that could also serve as biomarkers. Estimated mean levels of Nap and Phe associated with the nominal 100 microg/m3 DE were 2600 and 765 ng/m3 with estimated exposure ratios of 252 and 92.4, respectively. Nap levels were significantly correlated with OC and total particle-bound polycyclic aromatic hydrocarbons (PAHs); Phe levels were significantly correlated with total volatile + semivolatile PAHs. These results suggest that Nap and Phe may be particularly useful surrogates for DE concentrations. While Nap and Phe are not validated here as internal biomarkers of DE exposure, we are currently assessing human biological specimens collected during this study and will discuss those results in ensuing papers.

Occurrence of coal and coal-derived particle-bound polycyclic aromatic hydrocarbons (PAHs) in a river floodplain soil

A PAH contaminated river floodplain soil was separated according to grain size and density. Coal and coal-derived particles from coal mining, coal industry and coal transportation activities were identified by organic petrographic analysis in our samples. Distinct concentrations of PAHs were found in different grain size and density fractions, however, similar distribution patterns of PAHs indicated similar sources. In addition, although light fractions had the mass fraction by weight of less than 5%, they contributed almost 75% of the total PAHs in the soil. PAH concentrations of all sub fractions showed positive correlation with their TOC contents. Altogether, coal and coal-derived particles that were abundant in light fractions could be the dominant geosorbents for PAHs in our samples.

Detection of particle-phase polycyclic aromatic hydrocarbons in Mexico City using an aerosol mass spectrometer

We report the quantification of ambient particle-bound polycyclic aromatic hydrocarbons (PAHs) for the first time using a real-time aerosol mass spectrometer. These measurements were carried out during the Mexico City Metropolitan Area field study (MCMA-2003) that took place from March 29 to May 4, 2003. This was the first time that two different fast, real-time methods have been used to quantify PAHs alongside traditional filter-based measurements in an extended field campaign. This paper focuses on the technical aspects of PAH detection in ambient air with the Aerodyne AMS equipped with a quadrupole mass analyzer (Q-AMS), on the comparison of PAHs measured by the Q-AMS to those measured with the other two techniques, and on some features of the ambient results. PAHs are very resistant to fragmentation after ionization. Based on laboratory experiments with eight PAH standards, we show that their molecular ions, which for most particulate PAHs in ambient particles are larger than 200 amu, are often the largest peak in their Q-AMS spectra. Q-AMS spectra of PAH are similar to those in the NIST database, albeit with more fragmentation. We have developed a subtraction method that allows the removal of the contribution from non-PAH organics to the ion signals of the PAHs in ambient data. We report the mass concentrations of all individual groups of PAHs with molecular weights of 202, 216, 226 + 228, 240 + 242, 250 + 252, 264 + 266, 276 + 278, 288 + 290, 300 + 302, 316 and 326 + 328, as well as their sum as the total PAH mass concentration. The time series of the Photoelectric Aerosol Sensor (PAS) and Q-AMS PAH measurements during MCMA-2003 are well correlated, with the smallest difference between measured PAH concentrations observed in the mornings when ambient aerosols loadings are dominated by fresh traffic emissions. The Q-AMS PAH measurements are also compared to those from GC–MS analysis of filter samples. Several groups of PAHs show agreement within the uncertainties, while the Q-AMS measurements are larger than the GC–MS ones for several others. In the ambient Q-AMS measurements the presence of ions tentatively attributed to cyclopenta[ cd]pyrene and dicyclopentapyrenes causes signals at m/ z 226 and 250, which are significantly stronger than the signals in GC–MS analysis of filter samples. This suggests that very labile, but likely toxic, PAHs were present in the MCMA atmosphere that decayed rapidly due to reaction during filter sampling, and this may explain at least some of the differences between the Q-AMS and GC–MS measurements.

Characteristics of Ambient Particle-bound Polycyclic Aromatic Hydrocarbons in the Angkor Monument Area of Cambodia

The characteristics of ambient particle-bound polycyclic aromatic hydrocarbons (PAHs) in the Angkor monument area of Cambodia were studied to evaluate the status of air pollution and the influence of possible emission sources. Ambient particulates were sampled at four sites during the same seasons: Angkor monument area, including Angkor Wat, in Siem Reap city, along a main road, and on a small hill beside Lake Tonle Sap. Monitoring of ambient particles in the city and Angkor Wat were conducted on a continuous basis. Meteorological data were continuously monitored at two sites to evaluate the role of wind in the transport of pollutants. The concentrations of total suspended particulates (TSP), PAHs and heavy metals were analyzed to examine the influence of anthropogenic emissions, as well as contributions from soil and miscellaneous particles. Profiles of 15 PAH compounds were compared to determine the influence of wind direction on the seasonal characteristics of PAHs. TSP concentration proved to be proportional to the sum of the concentrations of Al, Ca and Fe, which were the major metals present in particles, regardless of location and season. The mass fraction of PAHs with 4-6 rings in Angkor Wat was almost equal to, or larger than, that found in the city. During the rainy season’s southwest monsoon, the PAH profile in Angkor Wat was similar to that found in the city, while it was similar to that found in the rural areas during the dry season’s north, or northeast, monsoon. This indicates that in the rainy season air pollutant transport from the city to the monument is an important factor. PAH concentration in Angkor Wat was similar to that measured in Bangkok, indicating a serious air pollution situation.

Characteristic study of polycyclic aromatic hydrocarbons for fine and coarse particulates at Pastureland near Industrial Park sampling site of central Taiwan

The concentrations of ambient air polycyclic aromatic hydrocarbons were measured in a farm area (Tunghai University Pastureland) between August 2001 and April 2002 in central Taiwan, Taichung. Particle-bound polycyclic aromatic hydrocarbons (PAHs) were collected on quartz filters, the collected sample was extracted with a dichloromethane (DCM)/ n-hexane mixture (50/50, v/v) for 24 h, and then the extracts were subjected to gas chromatography–mass spectrometric analysis. The PM 2.5 (fine particulate) and PM 2.5–10 (coarse particulate) total PAHs concentrations at the Tunghai University Pastureland sampling site were found to be 180.62 ng m −3 and 164.98 ng m −3, respectively. In general, the concentrations of polycyclic aromatic hydrocarbons were higher in spring and winter than those of summer and autumn for either PM 2.5 or PM 2.5–10 in Pastureland in central Taiwan. Moreover, coarse particulates are the dominant species during the dust storm season (March and April) in central Taiwan.

Characterization of Polycyclic Aromatic Hydrocarbons and Carbonyl Compounds in Diesel Exhaust Emissions

Exhaust emissions from a recent model heavy-duty diesel vehicle (city bus) in a chassis dynamometer were measured during a transient driving cycle. Particle-bound polycyclic aromatic hydrocarbons (PAHs) and gaseous carbonyls, substances that create health hazards and are, as yet, unregulated were collected, the former on filters and the latter on dinitrophenylhydrazine (DNPH)-coated silica cartridges and analysed by GC-MS and HPLC, respectively. PAH emission rates decreased with the number of benzene fused rings. They averaged 0.2 mg km(-1) for a total of 11 PAHs ranging from fluoranthene to benzo(ghi)perylene. Fluoranthene and pyrene accounted for 90% of total PAHs. The sum of emission rates of C1 approximately C6 carbonyls averaged 174 mg km(-1), even if formaldehyde alone represented approximately 70% of the total carbonyl mass, followed by acetaldehyde (13%). Results obtained were compared with emission data reported in previous studies.