scholarly journals Polycyclic aromatic hydrocarbons (PAHs) in road dust collected from Quang Ninh: Contamination levels and potential sources

2021 ◽  
Vol 37 (1) ◽  
Author(s):  
Nguyen Thuy Ngoc ◽  
Truong Thi Kim ◽  
Phan Thi Lan Anh ◽  
Duong Hong Anh ◽  
Phung Thi Vi ◽  
...  
Keyword(s):  
Polycyclic Aromatic Hydrocarbons ◽  
Aromatic Hydrocarbons ◽  
Road Dust ◽  
Diagnostic Ratios ◽  
Two Cities ◽  
Polycyclic Aromatic ◽  
The Common ◽  
Contamination Levels ◽  
Total Concentrations ◽  
Quang Ninh

Twenty road dust samples were collected from Ha Long and Cam Pha cities in Quang Ninh province for analysis of polycyclic aromatic hydrocarbons (PAHs) on the USEPA priority pollutant list. Total concentrations of sixteen PAHs in road dust samples of Ha Long and Cam Pha ranged from 232 - 593 ng/g d.w (average: 399 ng/g d.w) and 297 - 1624 ng/g d.w (average: 780 ng/g d.w), respectively. Proportitions of invididiuals were decreased in the order Phe (21% ± 13%) > Pyr (12% ± 6%) > Nap~Fluth (11% ± 6%) > BbF (10% ± 8%), suggesting the similar composition of analyzed PAHs in road dust at two cities. Based on the common diagnostic ratios for the identification of PAHs emission sources, the Fluth/(Fluth+Pyr) ratio (average: 0.43, range: 0.29-0.60), the BaA/(BaA+Chr) ratio (average: 0.30, range: 0.08-0.38), the IcdP/(IcdP+BghiP) ratio (average: 0.30, range: 0.22-0.46) and the BaP/BghiP ratio (average: 0.47 < 0.9) indicated that emissions from traffic activities may be the important sources of PAHs in Quang Ninh.

scholarly journals DISTRIBUTION AND SOURCES OF POLYCYCLIC AROMATIC HYDROCARBONS IN AQUATIC SEDIMENT FROM CAN GIO COASTAL WETLAND, HOCHIMINH CITY

2018 ◽  
Vol 54 (4B) ◽  
pp. 109
Author(s):  
Hoang Thi Thanh Thuy
Keyword(s):  
Polycyclic Aromatic Hydrocarbons ◽  
Aromatic Hydrocarbons ◽  
High Performance ◽  
Surface Sediments ◽  
Coastal Wetland ◽  
Diagnostic Ratios ◽  
Spatial Trend ◽  
Polycyclic Aromatic ◽  
Aquatic Sediment ◽  
Total Concentrations

The distribution of fifteen polycyclic aromatic hydrocarbons (PAHs) indicated from USEPA as priority pollutants was studied in surface sediments (0 - 20 cm) of coastal wetland area of Can Gio district, Hochiminh City. PAHs were recovered from the sediments by solvent extraction and then analyzed by means of high performance liquid chromatography system. Total concentrations of the ∑PAHs in the range 5 – 38 ng/g dw were detected, and a distinct spatial trend was observed. The contents of Nap, Ace, Flu, Phe and dBA were below detection limit. Diagnostic ratios such as benzo[a]anthracene/chrysene and fluoranthene/pyrene were achieved to evaluate the emission sources of PAHs. These ratios indicated an anthopogenic source (pyrolysis) of PAHs for sediments. Furthermore PAHs were associated mainly with fine particle sediments. Although the PAHs contents were below Vietnamese standard but potential risk to ecosystem needs further study since the high percentages of carcinogenic PAHs.

Characterization, identification of ambient air and road dust polycyclic aromatic hydrocarbons in central Taiwan, Taichung

2004 ◽  
Vol 327 (1-3) ◽  
pp. 135-146 ◽  
Author(s):  
Guor-Cheng Fang ◽  
Cheng-Nan Chang ◽  
Yuh-Shen Wu ◽  
Peter Pi-Cheng Fu ◽  
I-Lin Yang ◽  
...  
Keyword(s):  
Polycyclic Aromatic Hydrocarbons ◽  
Aromatic Hydrocarbons ◽  
Road Dust ◽  
Ambient Air ◽  
Polycyclic Aromatic ◽  
Central Taiwan

scholarly journals Occurrence, Removal, and Mass Balance of Polycyclic Aromatic Hydrocarbons and Their Derivatives in Wastewater Treatment Plants in Northeast China

Toxics ◽  
2021 ◽  
Vol 9 (4) ◽  
pp. 76
Author(s):  
Rashid Mohammed ◽  
Zi-Feng Zhang ◽  
Chao Jiang ◽  
Ying-Hua Hu ◽  
Li-Yan Liu ◽  
...  
Keyword(s):  
Wastewater Treatment ◽  
Polycyclic Aromatic Hydrocarbons ◽  
Aromatic Hydrocarbons ◽  
Wastewater Treatment Plants ◽  
Principal Component ◽  
Diagnostic Ratios ◽  
Regression Methods ◽  
Polycyclic Aromatic ◽  
Meta Regression ◽  
Coal Composition

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.

scholarly journals Polycyclic Aromatic Hydrocarbons in PM2.5 and PM2.5–10 in Urumqi, China: Temporal Variations, Health Risk, and Sources

Atmosphere ◽  
2018 ◽  
Vol 9 (10) ◽  
pp. 412 ◽  
Author(s):  
Suwubinuer Rekefu ◽  
Dilinuer Talifu ◽  
Bo Gao ◽  
Yusan Turap ◽  
Mailikezhati Maihemuti ◽  
...  
Keyword(s):  
Molecular Weight ◽  
Polycyclic Aromatic Hydrocarbons ◽  
Aromatic Hydrocarbons ◽  
Coal Combustion ◽  
Temporal Variations ◽  
Diagnostic Ratios ◽  
Positive Matrix ◽  
Increasing Trend ◽  
Polycyclic Aromatic ◽  
The Mean

PM2.5 and PM2.5–10 samples were simultaneously collected in Urumqi from January to December 2011, and 14 priority polycyclic aromatic hydrocarbons (PAHs) were determined. The mean concentrations of total PAHs in PM2.5 and PM2.5–10 were 20.90~844.22 ng m−3 and 19.65~176.5 ng m−3 respectively, with the highest in winter and the lowest in summer. Above 80% of PAHs were enriched in PM2.5, which showed remarkable seasonal variations compared to coarse particles. High molecular weight (HMW) PAHs were predominant in PM2.5 (46.61~85.13%), whereas the proportions of lower molecular weight (LMW) and HMW PAHs in PM2.5–10 showed a decreasing and an increasing trend, respectively, from spring to winter. The estimated concentrations of benzo[a]pyrene equivalent carcinogenic potency (BaPeq) in PM2.5 (10.49~84.52 ng m−3) were higher than that of in PM2.5–10 (1.15~13.33 ng m−3) except in summer. The estimated value of inhalation cancer risk in PM2.5 and PM2.5–10 were 1.63 × 10−4~7.35 × 10−3 and 9.94 × 10−5~1.16 × 10−3, respectively, far exceeding the health-based guideline level of 10−4. Diagnostic ratios and positive matrix factorization results demonstrated that PAHs in PM2.5 and PM2.5–10 were from similar sources, such as coal combustion, biomass burning, coking, and petroleum combustion, respectively. Coal combustion was the most important source for PAHs both in PM2.5 and PM2.5–10, accounting for 54.20% and 50.29%, respectively.

Distribution and source estimation of polycyclic aromatic hydrocarbons in coastal sediments from Seto Inland Sea, Japan

2020 ◽  
Vol 17 (7) ◽  
pp. 488
Author(s):  
Hiroaki Tsuji ◽  
Waqar Azeem Jadoon ◽  
Yoko Nunome ◽  
Hideo Yamazaki ◽  
Satoshi Asaoka ◽  
...  
Keyword(s):  
Polycyclic Aromatic Hydrocarbons ◽  
Aromatic Hydrocarbons ◽  
Sediment Cores ◽  
Seto Inland Sea ◽  
Emission Sources ◽  
Osaka Bay ◽  
The Seto Inland Sea ◽  
Polycyclic Aromatic ◽  
Mean Concentration ◽  
Total Concentrations

Environmental contextPolycyclic aromatic hydrocarbons are carcinogenic environmental contaminants that tend to migrate into the sediments in oceans and seas. Their vertical distribution in sediments from the Seto Inland Sea matched their emission over time, which in turn reflected changes in energy sources and industrial activities in Japan. This study shows that human activities on land directly and significantly influence the concentration of polycyclic aromatic hydrocarbons in sediments. AbstractSeventeen polycyclic aromatic hydrocarbons (PAHs) were identified in sediment cores collected at several locations in the Seto Inland Sea in 2015 and 2016 to understand their spatial distribution and potential emission sources. PAHs were analysed using gas chromatography–mass spectrometry. The age of the sediment cores was analysed using radioisotopic dating techniques to reconstruct historical PAH emissions. The total concentrations of 17 PAHs in the sediment cores of Osaka Bay in 2015 were in the range of 108–2810ng g−1 dry weight (dw) with a mean concentration of 1050ng g−1 dw. The total concentrations of 17 PAHs in sediment cores from the Seto Inland Sea in 2016 were in the range of 52.6–941ng g−1 dw with a mean concentration of 313ng g−1 dw. The spatial distribution of PAHs showed the highest concentration in Osaka Bay and the lowest in Kii Channel in 2016. The horizontal PAH distribution showed a decreasing trend in concentrations from the estuary offshore to Osaka Bay and Aki-Nada. The vertical PAH distribution revealed that levels were higher before the 1980s–1990s, when oil consumption and industrial activities in the Osaka region reached a maximum in the 20th century. The diagnostic ratios of PAHs and a principal component analysis revealed three main emission sources of PAHs, industry, biomass burning and traffic activities.

scholarly journals Variability of polycyclic aromatic hydrocarbons and their oxidative derivatives in wintertime Beijing, China

2019 ◽  
Vol 19 (13) ◽  
pp. 8741-8758 ◽  
Author(s):  
Atallah Elzein ◽  
Rachel E. Dunmore ◽  
Martyn W. Ward ◽  
Jacqueline F. Hamilton ◽  
Alastair C. Lewis
Keyword(s):  
Polycyclic Aromatic Hydrocarbons ◽  
Gas Phase ◽  
Aromatic Hydrocarbons ◽  
Total Concentration ◽  
Diagnostic Ratios ◽  
Strong Positive Correlation ◽  
Night Time ◽  
Naphthalic Anhydride ◽  
Positive Correlation ◽  
Polycyclic Aromatic

Abstract. Ambient particulate matter (PM) can contain a mix of different toxic species derived from a wide variety of sources. This study quantifies the diurnal variation and nocturnal abundance of 16 polycyclic aromatic hydrocarbons (PAHs), 10 oxygenated PAHs (OPAHs) and 9 nitrated PAHs (NPAHs) in ambient PM in central Beijing during winter. Target compounds were identified and quantified using gas chromatography–time-of-flight mass spectrometry (GC-Q-ToF-MS). The total concentration of PAHs varied between 18 and 297 ng m−3 over 3 h daytime filter samples and from 23 to 165 ng m−3 in 15 h night-time samples. The total concentrations of PAHs over 24 h varied between 37 and 180 ng m−3 (mean: 97±43 ng m−3). The total daytime concentrations during high particulate loading conditions for PAHs, OPAHs and NPAHs were 224, 54 and 2.3 ng m−3, respectively. The most abundant PAHs were fluoranthene (33 ng m−3), chrysene (27 ng m−3), pyrene (27 ng m−3), benzo[a]pyrene (27 ng m−3), benzo[b]fluoranthene (25 ng m−3), benzo[a]anthracene (20 ng m−3) and phenanthrene (18 ng m−3). The most abundant OPAHs were 9,10-anthraquinone (18 ng m−3), 1,8-naphthalic anhydride (14 ng m−3) and 9-fluorenone (12 ng m−3), and the three most abundant NPAHs were 9-nitroanthracene (0.84 ng m−3), 3-nitrofluoranthene (0.78 ng m−3) and 3-nitrodibenzofuran (0.45 ng m−3). ∑PAHs and ∑OPAHs showed a strong positive correlation with the gas-phase abundance of NO, CO, SO2 and HONO, indicating that PAHs and OPAHs can be associated with both local and regional emissions. Diagnostic ratios suggested emissions from traffic road and coal combustion were the predominant sources of PAHs in Beijing and also revealed the main source of NPAHs to be secondary photochemical formation rather than primary emissions. PM2.5 and NPAHs showed a strong correlation with gas-phase HONO. 9-Nitroanthracene appeared to undergo a photodegradation during the daytime and showed a strong positive correlation with ambient HONO (R=0.90, P < 0.001). The lifetime excess lung cancer risk for those species that have available toxicological data (16 PAHs, 1 OPAH and 6 NPAHs) was calculated to be in the range 10−5 to 10−3 (risk per million people ranges from 26 to 2053 cases per year).

scholarly journals Residues of Persistent Organic Pollutants (POPs) in Agricultural Soils Adjacent to Historical Sources of Their Storage and Distribution—The Case Study of Azerbaijan

Molecules ◽  
2020 ◽  
Vol 25 (8) ◽  
pp. 1815 ◽  
Author(s):  
Aleksandra Ukalska-Jaruga ◽  
Karolina Lewińska ◽  
Elton Mammadov ◽  
Anna Karczewska ◽  
Bożena Smreczak ◽  
...  
Keyword(s):  
Polycyclic Aromatic Hydrocarbons ◽  
Aromatic Hydrocarbons ◽  
Environmental Protection Agency ◽  
Agricultural Soils ◽  
The United States ◽  
Natural Soil ◽  
Polycyclic Aromatic ◽  
High Concentrations ◽  
Total Concentrations

The aim of this study was to identify and examine the levels of organochlorine pesticides (OCPs), polycyclic aromatic hydrocarbons (PAHs), and polychlorinated biphenyls (PCBs) in soil collected from the surroundings of historical pesticide storage facilities on former agricultural aerodromes, warehouses, and pesticide distribution sites located in the most important agricultural regions in Azerbaijan. The conducted research included determination of three groups of POPs (occurring together), in the natural soil environment influenced for many years by abiotic and biotic factors that could have caused their transformations or decomposition. In this study, soil samples were collected in 21 georeferenced points located in the administrative area of Bilasuvar, Saatly, Sabirabad, Salyan and Jalilabad districts of Azerbaijan. Soil chemical analysis involved determination of organochlorine compounds (OCP): hexachlorocyclohexanes (HCHs) (three isomers α-HCH, β-HCH and γ-HCH) and dichlorodiphenyltrichloroethanes (DDTs) (six congeners 2,4′DDT; 4,4′DDT; 2,4′DDE; 4,4′DDE; 2,4′DDE; and 4,4′DDE); polycyclic aromatic hydrocarbons (PAHs): 16 compounds from the United States Environmental Protection Agency US EPA list and, PCBs (seven congeners identified with the following IUPAC numbers: 28, 52, 101, 118, 138, 153, and 180). Our research showed that OCPs reached the highest concentration in the studied areas. The total concentrations of OCPs ranged from 0.01 to 21,888 mg∙kg−1 with significantly higher concentrations of Σ6DDTs (0.01 μg kg−1 to 21880 mg kg−1) compared to ΣHCH (0.14 ng kg−1 to 166.72 µg kg−1). The total concentrations of PCBs in the studied soils was varied from 0.02 to 147.30 μg·kg−1 but only PCB138 and PCB180 were detected in all analyzed samples. The concentrations of Σ16 PAHs were also strongly diversified throughout the sampling areas and ranged from 0.15 to 16,026 mg kg−1. The obtained results confirmed that the agricultural soils of Azerbaijan contained much lower (up to by three orders of magnitude) concentrations of PCBs and PAHs than DDT. It is supported by the fact that PCBs and PAHs were not directly used by agriculture sector and their content results from secondary sources, such as combustion and various industrial processes. Moreover, the high concentrations of PAHs in studied soils were associated with their location in direct neighborhood of the airport, as well as with accumulation of contaminants from dispersed sources and long range transport. The high concentrations of pesticides confirm that deposition of parent OCPs have occurred from obsolete pesticide landfills.

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