scholarly journals Source Apportionment of Particle Bound Polycyclic Aromatic Hydrocarbons at an Industrial Location in Agra, India

2012 ◽  
Vol 2012 ◽  
pp. 1-10 ◽  
Author(s):  
Anita Lakhani

16 US EPA priority polycyclic aromatic hydrocarbons (PAHs) were quantified in total suspended ambient particulate matter (TSPM) collected from an industrial site in Agra (India) using gas chromatography. The major industrial activities in Agra are foundries that previously used coal and coke as fuel in cupola furnaces. These foundries have now switched over to natural gas. In addition, use of compressed natural gas has also been promoted and encouraged in automobiles. This study attempts to apportion sources of PAH in the ambient air and the results reflect the advantages associated with the change of fuel. The predominant PAHs in TSPM include high molecular weight (HMW) congeners BghiP, DbA, IP, and BaP. The sum of 16 priority PAHs had a mean value of 72.7 ± 4.7 ng m−3. Potential sources of PAHs in aerosols were identified using diagnostic ratios and principal component analysis. The results reflect a blend of emissions from diesel and natural gas as the major sources of PAH in the city along with contribution from emission of coal, coke, and gasoline.

2020 ◽  
Author(s):  
Tatiana Drotikova ◽  
Aasim M. Ali ◽  
Anne Karine Halse ◽  
Helena C. Reinardy ◽  
Roland Kallenborn

Abstract. Polycyclic aromatic hydrocarbons (PAHs) are not declining in Arctic air despite reductions in their global emissions. In Svalbard, the Longyearbyen coal-fired power plant is considered to be one of the major local source of PAHs. Power plant stack emissions and ambient air samples, collected simultaneously 1 km (UNIS) and 6 km (Adventdalen) transect distance, were analyzed (gaseous and particulate phases separately) for 22 nitro-PAHs, 9 oxy-PAHs and 16 parent PAHs by GC/ECNI/MS and GC-MS/MS. Results confirm low level of PAH emissions (∑16 PAHs = 1.5 µg kg−1 coal) from the power plant. Phenathrene, 9,10-anthraquinone, 9-fluorenone, fluorene, fluoranthene, and pyrene accounted for 85 % of the plant emission (not including naphthalene). A dilution effect was observed for the transect ambient air samples, 1.26 ± 0.16 and 0.63 ± 0.14 ng m−3 sum all 47 PAH derivatives for UNIS and Adventdalen, respectively. The PAH profile was homogeneous for these recipient stations with phenathrene and 9-fluorenone being most abundant. Principal component analysis, in combination with PAH diagnostic ratios and literature data on different source-specific markers, confirmed coal combustion, gasoline, and diesel traffic as the predominant sources of PAHs. Secondary atmospheric formation of 9-nitroanthracene and 2+3-nitrofluoranthene was evaluated and concluded. Results also indicate that ambient PAH concentrations were affected by precipitation events, and specific humidity is an essential parameter influencing PAH scavenging from the air. The present study contributes important data which can be utilized to eliminate uncertainties in model predictions that aim to assess the extent and impacts of Arctic atmospheric contaminants.


Toxics ◽  
2021 ◽  
Vol 9 (4) ◽  
pp. 76
Author(s):  
Rashid Mohammed ◽  
Zi-Feng Zhang ◽  
Chao Jiang ◽  
Ying-Hua Hu ◽  
Li-Yan Liu ◽  
...  

Polycyclic aromatic hydrocarbons (PAHs), 33 methylated PAHs (Me-PAHs), and 14 nitrated PAHs (NPAHs) were measured in wastewater treatment plants (WWTPs) to study the removal efficiency of these compounds through the WWTPs, as well as their source appointment and potential risk in the effluent. The concentrations of ∑PAHs, ∑Me-PAHs, and ∑NPAHs were 2.01–8.91, 23.0–102, and 6.21–171 µg/L in the influent, and 0.17–1.37, 0.06–0.41 and 0.01–2.41 µg/L in the effluent, respectively. Simple Treat 4.0 and meta-regression methods were applied to calculate the removal efficiencies (REs) for the 63 PAHs and their derivatives in 10 WWTPs and the results were compared with the monitoring data. Overall, the ranges of REs were 55.3–95.4% predicated by the Simple Treat and 47.5–97.7% by the meta-regression. The results by diagnostic ratios and principal component analysis PCA showed that “mixed source” biomass, coal composition, and petroleum could be recognized to either petrogenic or pyrogenic sources. The risk assessment of the effluent was also evaluated, indicating that seven carcinogenic PAHs, Benzo[a]pyrene, Dibenz[a,h]anthracene, and Benzo(a)anthracene were major contributors to the toxics equivalency concentrations (TEQs) in the effluent of WWTPs, to which attention should be paid.


2013 ◽  
Vol 67 (2) ◽  
pp. 337-348 ◽  
Author(s):  
Natasa Jovcic ◽  
Jelena Radonic ◽  
Maja Turk-Sekulic ◽  
Mirjana Vojinovic-Miloradov ◽  
Srdjan Popov

Data on polycyclic aromatic hydrocarbons (PAHs) in ambient air accessed at selected locations in the vicinity of the industrial zone of the city of Novi Sad, Serbia, have been presented and analyzed in order to determine seasonal and spatial variations and to identify emission sources of particle-bound PAHs. Previous studies have demonstrated that the major contributors of PAHs in urban areas are the emissions from vehicle exhaust, and emissions releases from industrial processes like aluminium production, creosote and wood preservation, waste incineration, cement manufacture, petrochemical and related industries, commercial heat/power production etc. The sampling campaigns have been conducted at three sampling sites, during the two 14-day periods. The first site was situated near industrial area, with a refinery, power plant and heavy-traffic road in the vicinity. The second site was located nearby the heavy traffic area, especially busy during the rush hour. The third site was residential district. Summer sampling period lasted from June 26th to July 10th 2008, while sampling of ambient air during the winter was undertaken from January 22nd to February 5th 2009. Eighty-four (84) air samples were collected using a high volume air sampler TCR Tecora H0649010/ECHO. 16 US EPA polycyclic aromatic hydrocarbons were determined in all samples using a gas chromatographer with a mass spectrometer as a detector (Shimatzu MDGC/GCMS-2010). The total average concentrations of PAHs ranged from 1.21 to 1.77 ng/m3 during the summer period and from 6.31 to 7.25 ng/m3 in the winter. Various techniques, including diagnostic ratio (DR) and principal component analysis (PCA), have been used to define and evaluate potential emission sources of PAHs. Diagnostic ratio analysis indicated that vehicles, diesel or/and gasoline, industrial and combustion emissions were sources of PAHs in the vicinity of the industrial zone. Additionally, principal component analysis was used to constrain the potential sources. The results showed that vehicles are the predominant source of particle-bound PAHs during the whole year, and stationary sources (thermal power and heating plant, oil refinery, individual furnaces) during the winter period.


2021 ◽  
Author(s):  
Mohsen Soleimani ◽  
Zohreh Ebrahimi ◽  
Nourollah Mirghaffari ◽  
Hossein Moradi ◽  
Nasibeh Amini ◽  
...  

Abstract Particulate matters (PMs) and their associated chemical compounds such as polycyclic aromatic hydrocarbons (PAHs) are important factors to evaluate air pollution and its health impacts particularly in developing countries. Source identification of these compounds can be used for air quality management. The aim of this study was to identify the sources of PM2.5-bound PAHs in Isfahan city, a metropolitan and industrialized area in central Iran. The PM2.5 samples were collected at 50 sites during one year. Source identification and apportionment of PAHs were carried out using diagnostic ratios (DRs) of PAHs and positive matrix factorization (PMF) model. The results showed that the concentrations of PM2.5 ranged from 8 to 291 µg/m3 with an average of 60.2 ± 53.9 µg/m3 whereas the sum of concentrations of the 19 PAH compounds (ƩPAHs) ranged from 0.3 to 61.4 ng/m3 with an average of 4.65 ± 8.54 ng/m3. The PAH compounds showed their highest and lowest concentrations in fall and summer, respectively. Applying DRs, suggested that the source of the PAHs were mainly from fuel combustion. The main sources identified by the PMF model were gasoline combustion (28 %) followed by diesel combustion (22 %), natural gas combustion (17 %), evaporative-uncombusted (13 %), industrial activities (11 %), and unknown sources (9 %). The results revealed that in addition to transportation and industrial activities, combustion of natural gas for heating systems as one of the PAHs source in PM2.5 should be managed in the metropolitan area.


2014 ◽  
Vol 2014 ◽  
pp. 1-9 ◽  
Author(s):  
Su Ding ◽  
Yunping Xu ◽  
Yinghui Wang ◽  
Xinyu Zhang ◽  
Liang Zhao ◽  
...  

Polycyclic aromatic hydrocarbons (PAHs) were analyzed for surface sediments and a sediment core from the Yellow River-dominated margin. The concentration of 16 USEPA priority PAHs in surface sediments ranged from 5.6 to 175.4 ng g−1dry weight sediment (dws) with a mean of 49.1 ng g−1 dws. From 1930 to 2011, the distribution of PAHs (37.2 to 210.6 ng g−1 dws) was consistent with the socioeconomic development of China. The PAHs’ concentration peaked in 1964 and 1986, corresponding to the rapid economic growth in China (1958–1965) and the initiation of the “Reform and Open” policy in 1978, respectively. The applications of molecular diagnostic ratios and principal component analysis suggest that PAHs are predominantly produced by the coal and biomass combustion, whereas the contribution of petroleum combustions slightly increased after the 1970s, synchronous with an increasing usage of oil and gas in China.


2010 ◽  
Vol 63 (2) ◽  
pp. 211-218 ◽  
Author(s):  
Joil José Celino ◽  
Henry Xavier Corseuil ◽  
Marilda Fernandes ◽  
Karina Santos Garcia

Fourteen polycyclic aromatic hydrocarbons (PAHs) included in the US Environmental Protection Agency's (EPA) priority pollutant list were analyzed using gas chromatography-mass spectrometry (GC--MS). Surface water sampling was undertaken in the Paraguaçu Estuary (Bahia), northern Brazil. Total PAH concentrations varied from 0.0029 to 0.1079 ng/L in the surface waters (main rivers, tributaries) with a mean value of 0.0344 ng/L. Such concentrations can be taken as background values for the studied region. The PAH profiles were dominated by low molecular weight PAHs (two- and three-ring components) in surface water samples. It indicated that PAHs in surface water may have its origin from oil or sewage contamination (petrogenic input). The collected data showed that petrogenic input was predominant at almost all the stations investigated. To discriminate pattern differences and similarities among the samples, a principal component analysis (PCA) was performed using a correlation matrix. PCA revealed the latent relationships among all the surface water from the investigated stations.


Atmosphere ◽  
2021 ◽  
Vol 12 (3) ◽  
pp. 337
Author(s):  
Supansa Chimjarn ◽  
Olivier Delhomme ◽  
Maurice Millet

Gas and particulate phase ambient air concentrations of polycyclic aromatic hydrocarbons (Ʃ16PAHs) were determined in Strasbourg, a large city located in the Alsace region of northeastern France, from May 2018 to March 2020, to study the evolution of their temporal variations and their potential origins. The analysis of PAHs was performed using a global analytical method permitting the quantification of pesticides, PAHs, and polychlorobiphenyls (PCBs). Filters and Carbon doped silicon carbide NMC@SiC foams were extracted by accelerated solvent extraction (ASE) followed by a solid-phase extraction (SPE). Afterwards, extracts were analyzed using gas chromatography coupled to tandem mass spectrometry (GC-MS/MS). Prior to analysis, a pre-concentration step based on solid-phase microextraction (SPME) was used with a polydimethylsiloxane (PDMS) 100 µm fiber. The average total (gas plus particulate) concentration of Ʃ16PAHs varied from 0.51 to 117.31 ng m−3 with a mean of 16.87 ng m−3, with higher concentrations in the cold season of more than 2.5-fold and 6-fold that in the warm season for the gas and particulate phases, respectively. Moreover, low molecular weight (LMW) (2-ring and 3-ring) and medium molecular weight (MMW) (4-ring) PAHs contribute dominantly to the gas phase, while the particulate phase is associated with MMW (4-ring) and high molecular weight (HMW) (5-ring and 6-ring) PAHs. Gas/particle partitioning coefficient (log Kp) was calculated, and values varied between −4.13 and −1.49. It can be seen that the log Kp increased with the molecular weight of the PAHs and that the log Kp is different between cold and warm seasons for HMW PAHs but not for LMW PAHs. Diagnostic ratios of PAHs, which were employed to estimate the primary source of PAHs in Strasbourg, indicate that fuel combustion and biomass/coal burning are the possible origins of PAHs in Strasbourg’s atmosphere.


2021 ◽  
Vol 16 (2) ◽  
pp. 607-621
Author(s):  
Ayobami Omozemoje Aigberua ◽  
Enetimi Idah Seiyaboh

The environmental menace caused by hydrocarbon releasing activities on water bodies have remained a cause for great concern. Such activities are accompanied by the release of highly toxic and carcinogenic polycyclic aromatic hydrocarbons (PAH), which are easily biomagnified across the food chain, ultimately aggravating adverse health conditions in human. This study was aimed at identifying the most important environmental contributors of PAHs in sediments of the Imiringi river. Owing to the activities of oil facilities among other anthropogenic influences, water bodies are inundated with hydrocarbon pollutants which settle within river bed sediments, thereby, playing an important role in the redistribution of contaminants. The applied diagnostic ratios (Phenanthrene/Anthracene, Fluorene/Fluorene + Pyrene, Fluoranthene/Fluoranthene + Pyrene, pyrogenic index and total index) revealed the presence of mixed source of PAHs (pyrogenic and petrogenic). PAH concentrations ranged from <0.01 to 3,965.4 µg/kg with most detected compounds exceeding regulatory limits. The high molecular mass PAHs (4 - 6 ring HPAHs) represents the primary source showing 94.29% distribution, while the low molecular mass PAHs (2 - 3 ring LPAHs) recorded trace concentrations of about 5.71% of total PAHs. Principal component analysis (PCA) revealed Indeno(1,2,3-cd)pyrene and Dibenz(a,h)anthracene as principal PAH components in the environment. In addition, Pearson correlation showed Benzo(k)fluoranthene and Benzo(b)fluoranthene as the most positively correlating PAH species in sediment. Overall, the midstream section of the river was relatively more polluted than the up and down-river locations. Most notably, HPAHs recorded higher concentrations than the LPAHs. This may be due to intensive agricultural practices such as bush incineration, while waste dumps along the river bank remain tangible pyrogenic PAH contributors. On the other hand, trace amounts of observed petrogenic PAHs in some locations are possibly spill-over’s from oil bunkering activities and infiltrations from nearby oil installations.


2019 ◽  
Vol 14 (No. 2) ◽  
pp. 84-93
Author(s):  
Hamid Al-Saad ◽  
Wisam Farid ◽  
Wasen Abdul-Ameer

The soil samples from 0–10 cm depth were collected from three areas (Center of Basrah – CB, Garmat Ali – GA, and Abu Al-Khasib – AK) located along the Shatt Al-Arab River (SR) delta in southern Iraq to estimate the distribution and sources of polycyclic aromatic hydrocarbons (PAHs). The PAH total concentrations in the soils decreased significantly from CB (72.16 ng/g dry weight (DW)), GA (36.48 ng/g DW), to AK (17.30 ng/g DW) gradually indicating the impact of pollution emissions on the distribution of PAHs in soils. The low (2 and 3 ring) and high (4, 5, and 6 ring) molecular weight PAHs accounted for 14%, 16%, 37%, 21%, and 12% respectively in CB soil, 24%, 31%, 29%, 7%, and 10% in GA soil and 40%, 29%, 17%, 8%, and 8% in AK soil. The high molecular weight PAHs predominated in CB soils and the low molecular weight PAHs dominated in GA and AK soils suggesting a difference in emission sources between the studied areas. The PAH diagnostic ratios and principal component analysis (PCA) indicated that PAHs in soils of the SR delta essentially originated from traffic and industrial emissions and biomass and grass/wood/coal combustion. The PAH atmospheric transport from CB area might impact the PAH distribution in the soils of AK area. The risk assessment of the soils has been performed. The total toxic equivalent concentrations (Bap<sub>teq</sub>) of PAHs in the examined areas did not exceed the Dutch target values suggesting that no carcinogenic risk for the SR delta soils was found.  


2021 ◽  
Vol 33 (2) ◽  
pp. 439-446
Author(s):  
S.Y. Pang ◽  
S. Suratman ◽  
J.H. Tay ◽  
N. Mohd Tahir

The surface distributions of aliphatic hydrocarbons and polycyclic aromatic hydrocarbons (PAHs) were investigated from coastal sediments of Brunei Bay, southern South China Sea. The concentrations of total n-alkane (TNA) and 16 USEPA priority PAHs ranged from 0.67 to 9.88 μg/g and 4.72 to 102 ng/g, respectively. Principal component analysis (PCA) clustered the hydrocarbons in surface sediments according to their relationship and geographical locations, anticipated to the inputs and activities in proximity. Biomarker diagnostic ratios revealed that biogenic n-alkane inputs in the coastal sediments are exported from the fluviomarine and mangrove swamp environment, while the PAHs inputs are derived from mixed petrogenic and petroleum combustion residues. Overall, the level of PAHs in the study area is between low to moderate, based on the comparison with other areas worldwide.


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