Petroleum Combustion Research Articles

Polyaromatic hydrocarbon and chlorinated pesticides pollution in Iacob Lake of Romania: radionuclide-dated sediments and chromatographic analysis

This study aims to assess the persistent organic pollutant (POP) pollution history of Iacob Lake, Danube Delta, Romania. For this purpose, 16 polycyclic aromatic hydrocarbons (PAHs) and 20 organochlorine pesticides (OCPs) were determined by gas chromatography coupled with specific detectors in the lake sediment core collected in 2014. Before POP analysis, the sediment layers were dated using the 210Pb dating method. The target compounds were isolated from the sediment by ultrasound-assisted extraction, followed by extract clean-up by open-column chromatography. The obtained results showed that between 1940 and 2012, the concentrations of PAHs and OCPs in the dry-weight sediment layers ranged from 73.81 to 214.54 ng g−1 and from 71.78 to 192.69 ng g−1, respectively. Different PAH and OCP diagnostic ratios were used to identify and assess pollution sources. Our results show that the main sources of PAHs in Iacob Lake are mixed petroleum spills, biomass, coal, and petroleum combustion, while OCP residues come from legacy uses. Referring to the Sediment Quality Guidelines, the mean effect range-median quotient, and the toxic equivalent factor, it was found that the highest ecological risks occurred for the pesticide DDT, while the ecological risk for PAHs was considerably low.

Characterization of AhR-mediated potency in sediments from Kongsfjorden, Svalbard: Application of effect-directed analysis and nontarget screening

In this study, we aimed to identify the major aryl hydrocarbon receptor (AhR) agonists in surface sediments (S1–S10, n = 10) from Kongsfjorden, Arctic Svalbard, using effect-directed analysis. High AhR-mediated potencies were observed in the mid-polar fractions and RP-HPLC subfractions (F2.6–F2.8; log KOW 5–8) in the sediments of sites S2 and S3, which are located near abandoned coal mine areas, as assessed by the H4IIE-luc bioassay. The concentrations of traditional polycyclic aromatic hydrocarbon (t-PAHs), emerging PAHs, alkyl-PAHs, and styrene oligomers ranged from 6.1 to 2100 ng g−1 dry weight (dw), 0.5–1000 ng g−1 dw, 47 to 79,000 ng g−1 dw, and 4.2–130 ng g−1 dw, respectively, with elevated levels in S2 and S3. Principal component analysis coupled with multiple linear regression suggested that t-PAHs in sediments primarily originated from coal, petroleum combustion, and coal combustion. Twenty-four target AhR agonists accounted for 3.2%–100% (mean = 47%) of the total AhR-mediated potencies in S2 and S3. Nontarget screening via GC-QTOFMS in the highly potent fractions identified 48 AhR agonist candidates through four-step selection criteria. Among these, 27 compounds were identified as coal-derived substances. VirtualToxLab in silico modeling predicted that most of the 48 tentative AhR agonist candidates could bind to AhR. Overall, our findings indicate significant contamination of the Kongsfjorden sediments by coal-derived substances, highlighting the need for further studies to assess the ecological risks associated with these contaminants.

Chemical Fingerprinting, PAHs Characterization and Ecological Risks of Carcinogenic PAHs in Surficial Sediments of Egi Crude Oil Producing Communities, Niger-Delta, Nigeria

In order to do PAHs rings analysis, its source identification, extent to which cPAHs present and what kind of ecological risk they pose, the surface sediments from various freshwaters in the Egi crude oil producing cities in the Niger Delta, Nigeria were analyzed. Sediments collected from the research areas for PAHs loadings (in mg/kg dry weight) ranged from 0.020 to 1.790, 0.050 to 1.880, and 0.020 to 1.640, respectively for Obite, Obagi, and Ibewa cluster areas, as measured by gas chromatography-mass spectrometer. In these clusters, the respective average concentration of the three dominant carcinogenic PAHs were Indeno(1,2,3-cd)pyrene (1.170.0mg/kg), Dibenz[a,h]anthrancene (0.870.0 mg/kg), and Dibenz[a,h]anthrancene (1.3670 mg/kg) for Ibewa, Obagi and Obite cluster areas. The findings showed that dominant PAHs rings are of high molecular weight (HMW) PAHs in these sediments are, 5 member rings, which are benzo(b)fluoranthene, Benzo(k)fluoranthene, and Benzo(a)pyrène, and 6-member ring which are, Indeno(1,2,3-cd)pyrene, Dibenz[a,h]anthrancene, and Benzo[ghi] perylene, respectively. Their fingerprints points majorly to pyrogenic sources, combustion of coal, biomass, petroleum, and other related anthropogenic petroleum activities as the primary source of PAHs in the environment. Notably, the RQNCs and RQMPCs for single PAHs molecule are both less than 1, it means the contamination it generates is considered of low ecological risk. Again, the research area experiences frequent flooding, it is believed that this contributes to the low ecological risk of PAHs chemical pollution. Consequently, the area is deemed to be quite safe.

The Global Biogeochemical Cycle of Rhenium

AbstractThis paper is the first comprehensive synthesis of what is currently known about the different natural and anthropogenic fluxes of rhenium (Re) on Earth's surface. We highlight the significant role of anthropogenic mobilization of Re, which is an important consideration in utilizing Re in the context of a biogeochemical tracer or proxy. The largest natural flux of Re derives from chemical weathering and riverine transport to the ocean (dissolved = 62 × 106 g yr−1 and particulate = 5 × 106 g yr−1). This review reports a new global average [Re] of 16 ± 2 pmol L−1, or 10 ± 1 pmol L−1 for the inferred pre‐anthropogenic concentration without human impact, for rivers draining to the ocean. Human activity via mining (including secondary mobilization), coal combustion, and petroleum combustion mobilize approximately 560 × 106 g yr−1 Re, which is more than any natural flux of Re. There are several poorly constrained fluxes of Re that merit further research, including: submarine groundwater discharge, precipitation (terrestrial and oceanic), magma degassing, and hydrothermal activity. The mechanisms and the main host phases responsible for releasing (sources) or sequestrating (sinks) these fluxes remain poorly understood. This study also highlights the use of dissolved [Re] concentrations as a tracer of oxidation of petrogenic organic carbon, and stable Re isotopes as proxies for changes in global redox conditions.

USE OF METHANOL AS MOTOR FUEL FOR MARINE INTERNAL COMBUSTION ENGINES

The international maritime organization's intention to reduce greenhouse gas emissions to the atmosphere by two times compared to 2008 by 2050 prompted manufacturers of marine engines to start actively searching for ways to solve this problem. Since significant global changes in the structure of ship power equipment are not expected during this period, the main efforts of researchers are aimed at solving the problem of reducing emissions based on piston engines, which today form the basis of ship power. The technology of the first stage of reducing greenhouse gas emissions was the conversion of marine diesels to gas fuels, and primarily to methane. These technologies, which are already widely used in water transport today, make it possible to reduce greenhouse gas emissions by 20...25%, but do not solve the problem completely. Today it is clear that a global solution to the problem is possible only when using as motor fuel compounds that are either carbon-free, i.e. do not contain carbon in their composition at all, or are carbon neutral, i.e. contain carbon extracted from the atmosphere by biological or technological means. One such compound is methyl alcohol or methanol. Today, most of the methanol in the world is produced either from coal or from natural gas, so the total emissions of greenhouse gases when burning such methanol even exceed emissions from burning petroleum fuels, however, unlike the latter, this compound can be obtained from biological raw materials, or by binding atmospheric carbon. Today, such methanol, which has received the name «green», is too expensive, and its production technologies require further development. This can happen only if there is international stimulation and regulation of this area of production. But the introduction of such regulation requires a clear understanding of the technical feasibility and economic and environmental feasibility of using methanol as a motor fuel. That is why leading manufacturers today are working on solving these issues. Their solution is considered the second stage on the way to the complete decarbonization of shipping, and at this stage there has been significant progress in recent years. This article is devoted to the analysis of the current state of the question regarding the use of methanol as motor fuel for ship engines of all types and sizes.

Chronological evaluation of polycyclic aromatic hydrocarbons in sediments of tangxun lake in central China and impacts of human activities.

This study sheds light on the contamination of polycyclic aromatic hydrocarbons (PAHs) in Tangxun Lake sediments, an urban lake reflecting environmental changes in Central China. By analyzing sediment cores from both the inner and outer areas of the lake, we determined the historical trends and sources of PAHs over the past century. The results reveal a significant increase in PAHs concentrations, particularly since the 1980s, coinciding with China's rapid urbanization and industrialization. Using diagnostic ratios and Absolute principal component score-multivariate linear regression (APCS-MLR) methods, we identified petroleum combustion, coal combustion, and biomass combustion as the primary sources of PAHs in the lake sediments. The spatial analysis indicates higher PAHs levels in the inner lake, likely due to its closer proximity to industrial activities. Moreover, by comparing PAH trends in Tangxun Lake with those in other urban, suburban, and remote lakes across China, based on data from 49 sedimentary cores, we highlight the impact of regional socio-economic dynamics on PAH deposition. These insights are crucial for developing effective pollution mitigation strategies and promoting sustainable development in rapidly urbanizing regions.

COVID-19 lockdown measures affect polycyclic aromatic hydrocarbons distribution and sources in sediments of Chaohu Lake, China

The COVID-19 pandemic has profoundly impacted human activities and the environment globally. The lockdown measures have led to significant changes in industrial activities, transportation, and human behavior. This study investigates how the lockdown measures influenced the distribution of polycyclic aromatic hydrocarbons (PAHs) in the sediments of Chaohu Lake, a semi-enclosed lake. Surface sediment samples were collected in summer of 2020 (lockdown have just been lifted) and 2022 and analyzed for 16 priority PAHs. The range of ΣPAHs concentrations remained similar between 2020 (158.19–1693.64 ng·g−1) and 2022 (148.86–1396.54 ng·g−1). Among the sampling sites, the west lake exhibited similar PAHs concentrations characteristics over the two years, with higher levels observed in areas near Hefei City. However, the east lake exhibited increased ΣPAHs concentrations in 2022 compared to 2020, especially the area near ship factory. PAHs source analysis using principal component analysis-multiple linear regression (PCA-MLR) revealed an increased proportion of petroleum combustion sources in 2022 compared to 2020. The isotope analysis results showed that organic matter (OM) sources in the western lake remained relatively stable over the two years, with sewage discharge dominating. In contrast, the eastern lake experienced a shift in OM sources from sewage to C3 plants, potentially contributing to the increased PAH levels observed in the eastern lake sediments. Ecological risk assessment revealed low to moderate risk in both 2020 and 2022. Health risk evaluation indicated little difference in incremental lifetime cancer risk (ILCR) values between the two years, with only benzo[a]pyrene (BaP) posing a high risk among the carcinogenic PAHs. Children generally faced higher health risks compared to adults. This study reveals pandemic-induced changes in PAH pollution and sources in lake sediments, offering new insights into the impact of human activities on persistent organic pollutants, with implications for future pollution control strategies.

Characteristics, sources, and health risks of PAHs and their derivatives in indoor dust in Zhengzhou

The occurrence, source, and health risk of polycyclic aromatic hydrocarbons (PAHs), nitro-PAHs (NPAHs), and oxy-PAHs (OPAHs) in indoor dust collected from three types of microenvironments (offices, classrooms, and dormitories) at a university campus in Zhengzhou were analysed. The results showed that the average concentration of the total PAHs was 2403.21 ± 981.99 ng g−1, with PHE (20.06% of Σ18PAHs) and BkF (15.46%) being the dominant species. The average concentrations of total NPAHs and OPAHs were 11.09 ± 5.12 and 385.80 ± 255.27 ng g−1, with 2+3N-FLT (39.15%) and 9-FLO (39.76%) as the most abundant species of NPAHs and OPAHs, respectively. The average concentrations of total PAHs, NPAHs, and OPAHs in different microenvironments displayed obvious spatial specificity with the highest values in dormitories. The main source of PAHs, as identified by diagnostic ratios, was petroleum combustion, coal/biomass combustion and vehicle exhaust emissions. The average incremental lifetime cancer risk (ILCR) for undergraduates exposed to dust in classrooms and dormitories exceeded 10−6, indicating a potential cancer risk. The most important exposure pathway was dermal contact, while the inhalation route was negligible.

Impact of PAHs compounds on air quality in Maragheh city: Probabilistic risk assessment and source apportionment

This study explores the concentrations and spatial distribution of polycyclic aromatic hydrocarbons (PAHs) in the ambient air of Maragheh city, Iran, while evaluating their potential health implications. PAHs levels were examined in PAHs-bound to particulate matter samples collected from diverse locations across the city. The results showed that in all sampling points, there was contamination by PAHs. The mean total PAHs concentration was 11.5 ng.m−3, with Benzo[a]pyrene (BaP) emerging as the predominant compound. Comparative analysis with other cities revealed relatively lower BaP levels in Maragheh, yet surpassing WHO guidelines in 92 % of samples. Spatial assessment heightened pollution in areas characterized by heavy traffic and industrial operations. Based on PCA analysis, it appears that 74 % of PAHs compounds originate from vehicle emissions, 13 % from the combustion of petroleum, and 6 % from a possible petroleum source. Health risk appraisal uncovered escalated carcinogenic and mutagenic hazards, especially among children. While risks remained below USEPA thresholds, ongoing monitoring and targeted interventions are advised to mitigate PAHs pollution in Maragheh and similar urban locales. Future endeavors should prioritize source elucidation, health impact assessments, and public awareness initiatives to safeguard community well-being.

Current Advances in Agriculture, Environment, and Chemistry with Technological Applications

Soil contaminated with heavy metals has a negative impact on plant development and survival. On the other hand, plants have developed intricate physiological mechanisms to resist these kinds of environmental stimuli. Anthropogenic sources of emissions are the many industrial point sources, including transporters, smelters and foundries, present and former mining sites, and combustion byproducts. Mercury is released via the degassing of the earth's crust, whereas lead is emitted during its mining and smelting operations, from automotive exhausts by burning petroleum fuels coated with tetraethyl lead antiknock, and from old lead paints. The process of refining zinc releases cadmium as a byproduct and occasionally lead. Emissions are generally released during the mining and processing of metals. Stress from heavy metals affects plants absorb nutrients through interactions with other essential elements. Chromium restricts the quantity of nutrients the soil may absorb by forming insoluble compounds. An intriguing method for managing plastic waste, particularly micro/nano plastics, is photocatalysis. Through the use of suitable light energy, nanostructured semiconductors are excited, producing exciton pairs that react with surrounding water or moisture to produce highly reactive species like superoxide’s and hydroxyl radicals that can effectively oxidize organic species, including polymers. Climate variability affects the sustainability of human and environmental health together with other man-made and natural stresses.

Assessment of organic contaminants at a paint manufacturing site: Implications for health risks and source identification

The daily variation of organic contaminants, both gaseous and associated with suspended particulate matter (PM), was investigated within the estate of the National Company of Paintings in Lakhdaria, Algeria, spanning the period 2014-2015. The research emphasizes the chemical characterization of suspended PM, analyzing a range of organic compounds, including n-alkanes, polycyclic aromatic hydrocarbons (PAHs), and highly polar organics (HPOC), such as phthalate esters and heterocyclic compounds. Vapors of PAHs and polychlorobiphenyls (PCBs) were also analyzed. Low molecular weight compounds were primarily associated with the gas phase (two-ring PAHs, approximately 95%; three-ring PAHs, around 70%), while high molecular weight congeners were mainly associated with the particle phase (six-ring PAHs, 55%). The concentrations of PCBs (ranging from 0.6 to 42 ng m–3) were higher than those reported in other cities in Algeria and Europe. The source reconciliation of organic contaminants through principal component analysis (PCA) demonstrated that the primary sources were petroleum combustion, industrial manufacturing, tobacco smoking, and vehicular traffic. The significance of tobacco smoke was further confirmed by the analysis of PAH diagnostic ratios. Differences in the rates of diagnostic ratios between gaseous and particulate PAHs were attributed to distinct contributions from sources such as industrial processes. Health risks for workers exposed to PAHs and PCBs in PM < 10 μm (PM10) were quantitatively assessed in terms of benzo[a]pyrene equivalent concentration and incremental lifetime cancer risk (ILCR). The ILCR presents novel findings showcasing heightened risks among workers exposed to specific PAHs within production areas, whereas those related to PCBs suggested a high potential of health risks for laboratory workers.

Dust dynamics: distribution patterns of semi-volatile organic chemicals across particle sizes in varied indoor microenvironments.

An extensive analysis of the distribution patterns of three distinct classes of semi-volatile organic chemicals (SVOCs)-phthalates (PAEs), organophosphate flame retardants (OPFRs), and polycyclic aromatic hydrocarbons (PAHs)-across four distinct size fractions of dust (25, 50, 100, and 200μm) was conducted. The dust samples were sourced from AC filter, covered car parking lots, households, hotels, mosques, and car floors. To generate the four fractions, ten dust samples from each microenvironment were pooled and sieved utilizing sieving apparatus with the appropriate mesh size. Selected SVOCs were quantified utilizing gas chromatography-mass spectrometry in electron impact (EI) mode. Results unveiled diverse contamination levels among dust fractions, showcasing car parking lot dust with the lowest chemical contamination, while car floor dust displayed the highest levels of PAHs and OPFRs, peaking at 28.3µg/g and 43.2µg/g, respectively. In contrast, mosque and household floor dust exhibited the highest concentrations of phthalates, with values of 985µg/g and 846µg/g, respectively. Across the analyzed microenvironments, we observed a trend where concentrations of SVOCs tended to rise as dust particles decreased in size, forming a visually striking pattern. This phenomenon was particularly pronounced in dust samples collected from car floors and parking lots. Among SVOCs, PAEs emerged as the predominant contributors with > 90% followed by OPFRs and PAHs. The high levels of OPFRs in car floor dust align logically with the fact that numerous interior components of cars are treated with OPFRs, within a compact indoor microenvironment, to comply to fire safety regulations. Furthermore, petroleum products are a major source of PAHs in the environment and all the sampled cars in the study had combustion engines. Consequently, car dust is more likely to be polluted with PAHs stemming from petroleum combustion. Although previous investigations have noted an increase in heavy metals and brominated flame retardants with decreasing dust particles, this is the first study analyzing these SVOCs in different fractions of dust from various microenvironments. However, aside from two specific microenvironments, the observed pattern of escalating SVOC concentrations with smaller dust particle sizes was not corroborated among the examined microenvironments. This divergence in concentration trends suggests the potential involvement of supplementary variables in influencing SVOC distributions within dust particles.

Polycyclic aromatic hydrocarbons and their halogenated derivatives in soil from Yellow River Delta: Distribution, source apportionment, and risk assessment

The distribution of polycyclic aromatic hydrocarbons (PAHs) and halogenated PAHs (HPAHs) in surface soils from the petroleum industrial area of the Yellow River Delta (YRD) in China were investigated. The total concentrations of 16 PAHs ranged from 19.6 to 1560 ng/g, while 22 HPAHs ranged from 2.44 to 14.9 ng/g. Moreover, a high degree of spatial distribution heterogeneity was observed for both PAHs and HPAHs, which is likely attributed to the distinct industrial activities in studied area. The combustion of biomass and petroleum were identified as primary sources of soil PAHs and HPAHs in the YRD. Furthermore, benzo[b]fluoranthene, benzo[k]fluoranthene, and benzo[g,h,i]perylene exhibited high ecological risks (with risk quotients of 1.47, 1.44, and 1.02, respectively) in specific sites within the YRD. Considering the high toxicity of HPAHs and their potential joint environmental effects with PAHs, continuous attention should be directed towards the environmental risks associated with both PAHs and HPAHs.

Spatiotemporal distributions and ecological risk of polycyclic aromatic hydrocarbons in the surface seawater of Laizhou Bay, China.

The spatial-temporal distribution, source, and potential ecological risk of polycyclic aromatic hydrocarbons (PAHs) in surface seawater from Laizhou Bay were investigated. The total PAH (ΣPAH) concentrations ranged from 277 to 4393 ng/L with an average of 1178 ng/L, thereby suggesting a relatively moderate to high PAH exposure level in Laizhou Bay in comparison to other bays in the world. The composition patterns and source apportionment results revealed that the coal, biomass burning, diesel emissions, and petroleum combustion as well as the combination of these processes were the dominant sources of PAHs in the surface water, which were closely associated with sail process and sewage effluents. The ecological risk assessment indicated that benzo(a)pyrene (BaP), phenanthrene (Phe), luoranthene (Flua), and naphthalene (Nap) would exist ecological risks in most of surface seawater sites, but the probabilistic risk assessment (PRA) results showed that the current level of risk is not as severe as the risk quotient (RQ) results revealed.

Sedimentary records of polycyclic aromatic hydrocarbons and organochlorine pesticides to reconstruct anthropogenic activities in Lake Issyk-Kul region (Kyrgyzstan), and their effects on the lake environment

Vertical distributions of polycyclic aromatic hydrocarbons (PAHs) and organochlorine pesticides (OCPs) in a sediment core from Lake Issyk-Kul are powerful tools for reconstructing historical anthropogenic activities over the past 350 years. Four periods were identified according to the variations in these environmental proxies. Period Ⅰ (1670s–1800s) corresponds to a phase of limited anthropogenic activity reflected by the lowest ΣPAH16 concentrations, mainly from biomass combustion and petrogenic processes. Along with pronounced deforestation due to wildfires documented in the pollen record, a similar decrease in PAHs suggests that PAHs were most likely generated by natural sources around Lake Issyk-Kul during this period. Period Ⅱ (1800s–1930s) reflects increasing agricultural activities with fluctuations in various PAH concentrations. Anthropogenic biomass-derived PAH inputs from agricultural activities gradually replaced natural inputs to Lake Issyk-Kul, coinciding with several historical events. However, natural factors still mainly controlled changing lake levels before the 1930s. Period Ⅲ (1930s–1970s) corresponds to rapid development of agricultural activities, inferred by slight increases in ΣPAH16 concentrations dominated by coal-derived PAHs and a considerable increase in ΣOCP18 concentrations. Concentrated agricultural activities around Lake Issyk-Kul significantly influenced environmental changes in grain size and water level in the lake. Period Ⅳ (post-1970 s) corresponds to intensive industrial and urban activities, including a 10-year economic depression (1990s–2000s), characterized by the highest ΣPAH16 concentrations mainly from petroleum combustion followed by a sharp drop after the 1990s as the dissolution of the Soviet Union. Industrialization and urbanization in study area have changed the trophic state of Lake Issyk-Kul, particularly in recent years. Climate change has also induced “lateral remobilization” of contaminants, increasing pollution levels in this mountain lake.

Study on the Aral Sea crisis from the risk assessment of polycyclic aromatic hydrocarbons and organochlorine pesticides in surface water of Amu Darya river basin in Uzbekistan

The Amu Darya River, as one of the important flows of the Aral Sea located in the semi-arid area of Central Asia, also performed as the primary water supply for Uzbekistan. Therefore, the residues and risks of anthropogenic-related persistent organic pollutants (POPs) in waters of the Amu Darya River were conducted in the present study to elucidate their possible effects on the water safety in such a specific area as well as on the Aral Sea Crisis from a new perspective. Thirty-nine water samples distributed along the Amu Darya River to the coastal of the Aral Sea were analyzed for both polycyclic aromatic hydrocarbons (PAHs) and organochlorine pesticides (OCPs) occurrence, showing the total concentrations of ΣOCPs and ΣPAHs in the range of 1.16–22.75 ng/L and 3.18–506.26 ng/L, respectively. Spatial differences showed higher levels for both OCPs and PAHs along the lower reaches of the Amu Darya River due to intense human activities. Source identification performed by isomer ratios indicated that dichlorodiphenyltrichloroethanes (DDTs) probably originated from recent use, while hexachlorocyclohexanes (HCHs), chlordanes, and endosulfans originated mainly from historical usage. Furthermore, the principal component analysis showed PAHs were from coal and petroleum combustion (65.2%), biomass combustion (27.2%), and industrial chemical combustion (7.64%). The human health risk assessment demonstrated no carcinogenic or non-carcinogenic risks at present. However, moderate to high ecological risks to aquatic organisms especially were observed along the lower reaches, especially the delta area. The results obtained would not only provide important basic data for such a semi-arid area but also show us the possible toxic effects induced by such pollutants, which should attract more attention in the shrinking case of the Aral Sea.

Seasonal and Emission Characteristics of PAHs in the Ambient Air of Industrial Complexes

Particulate and gaseous polycyclic aromatic hydrocarbon (PAHs) samples (n = 108) were measured every six days from January to December 2022 at a representative point in the Korean Banwol National Industrial Complex. The measurement results revealed that the concentration of particulate Σ18 PAHs was 7.92 ± 4.04 ng/Sm3 in winter, 1.83 ± 1.99 ng/Sm3 in spring, 1.43 ± 0.95 ng/Sm3 in summer, and 2.58 ± 2.14 ng/Sm3 in autumn. The concentration of gaseous Σ18 PAHs was 3.32 ± 3.72 ng/Sm3 in winter, 6.34 ± 5.95 ng/Sm3 in spring, 8.33 ± 8.13 ng/Sm3 in summer, and 3.88 ± 1.71 ng/Sm3 in autumn. The results of the correlation analysis showed that particulate PAHs have positive relationships with PM10 and PM2.5 and negative relationships with temperature and O3. The diagnostic ratio and PAHs component slope showed that the emission source characteristics of the Banwol National Industrial Complex were dominated by biomass coal combustion over four seasons; however, the influence of petroleum combustion (automobile emissions) was not negligible. As for coal combustion, bituminous coal was the most influential, and lignite was relevant in summer and autumn.

Pollution Assessment with Persistent Organic Pollutants in Upper Soil of a Series of Rural Roma Communities in Transylvania, Romania, Its Sources Apportionment, and the Associated Risk on Human Health

This paper aims to assess the pollution by determining the sources of persistent organic pollutants (POPs) in 22 rural Roma communities in Transylvania in order to assess the human health risk associated with this exposure. For this, 16 polycyclic aromatic hydrocarbons (PAHs), 20 organochlorine pesticides (OCPs) and 12 polychlorinated biphenyls (PCBs) were determined in 22 soil samples collected from selected areas by gas chromatography coupled with mass spectrometry for PAHs and with electron capture detector for all halogenated compounds. Target compounds were isolated from soil by ultrasound-assisted extraction. We found that POP concentrations in soil ranged from 4.86 to 451.85 ng/g dw for PAHs, from 25.62 to 139.30 ng/g dw for OCPs, and from 0.22 to 49.12 ng/g dw for PCBs. The diagnostic ratios ƩLMW/ƩHMW, ANT/(ANT + PHE), and FLT/(FLT + PYR) strongly suggest a pyrogenic model of PAHs, such as biomass, coal, and petroleum combustion, while the isomer ratios ƩDDT/ƩHCH, α-HCH/γ-HCH and (DDE + DDD)/ƩDDT suggest that OCP residues originate from their ancient uses. Non-carcinogenic (HI) and carcinogenic (CR) risks of these organic compounds present in the soil through non-dietary pathways were in the very low-risk category (ranging from 10−8 to 10−4), indicating an absence of these risks from the investigated POPs in the studied area.

Characteristics, source, and health risk assessment of aerosol polyaromatic hydrocarbons in the rural and urban regions of western Saudi Arabia

Abstract Air quality represents one of the most important parameters determining indoor microclimate and human comfort. Thus, the current study reports a comprehensive study on the dominant sources, organic compositions, and potential health impacts of the polyaromatic hydrocarbons (PAHs) in the atmospheric particle matters (PMs) ranging from 2.5 µm (PM2.5) to 10 µm (PM10) size in the rural and urban regions of western (Jeddah city) Saudi Arabia collected over 1 year between 2014 and 2015. The levels of PAHs in two locations namely Obhur (Urban) and Hada Alsham (Rural) were monitored over 1 year (2014 and 2015) using the gas chromatography coupled mass spectrometry. The level of ƩPAHs in Obhur (819.25 ng/m3) has a significantly high concentration of PAHs compared to Hada Alsham (Rural) (675.26 ng/m3). Indeno(1,2,3-CD)pyrene was the major contributor with an average value of 215.66 ng/m3 followed by benzo[k]fluranthene with a concentration of 150.68 ng/m3, respectively. The major contributors were indeno[1,2,3-cd]pyrene, benzo[k]fluranthene, dibenzo[a,h]anthracene, benzo[g,h]perylene, and benzo[b]fluranthene are the major contributors with contributing percentages of 26.32, 18.39, 9.07, and 8.29%, respectively. The rest of all compounds were below 4%. The highest concentrations of PAHs in Obhur (1836.99 ng/m3) and in Hada Alsham (1107.40 ng/m3) were observed in winter in January 2014. PAHs with 4–6 aromatic ring components are primarily emitted by high temperature combustion. The average values for the BaA/(BaA + Chr) and Flt/(Flt + Pyr) ratios at Obhur were found 0.58 and 0.43 and at Hada Alsham were found 0.63 and 0.38, respectively, indicating that coal/biomass burning is the major source of PAHs. Hada Alsham (rural area), the transportation system, is a significant contributor to the observed PAHs. These results reflect Saudi Arabia’s traffic load in both rural and urban areas. On road sites, the impact of petroleum combustion and vehicular emissions was also identified. The sum of the incremental lifetime cancer risk (ILCR) for all congeners for infants along the Obhur location was 2.13 × 10−6 and 1.38 × 10−6, respectively. ILCR values were less than 1.0 × 10−4, implying that PAH exposure posed an acceptable potential cancer risk in this study. Various local emission sources contributed more PAHs in many Saudi urban areas, increasing the risk of lung cancer, and the health risk. PAHs have an associated large surface area and are capable of deposition in the respiratory system with high efficiency. The total health risk assessment study also helps in alarming the toxicity at both the locations.

Characteristics, source, and health risk assessment of aerosol polyaromatic hydrocarbons in the rural and urban regions of western Saudi Arabia

Abstract Air quality represents one of the most important parameters determining indoor microclimate and human comfort. Thus, the current study reports a comprehensive study on the dominant sources, organic compositions, and potential health impacts of the polyaromatic hydrocarbons (PAHs) in the atmospheric particle matters (PMs) ranging from 2.5 µm (PM2.5) to 10 µm (PM10) size in the rural and urban regions of western (Jeddah city) Saudi Arabia collected over 1 year between 2014 and 2015. The levels of PAHs in two locations namely Obhur (Urban) and Hada Alsham (Rural) were monitored over 1 year (2014 and 2015) using the gas chromatography coupled mass spectrometry. The level of ƩPAHs in Obhur (819.25 ng/m3) has a significantly high concentration of PAHs compared to Hada Alsham (Rural) (675.26 ng/m3). Indeno(1,2,3-CD)pyrene was the major contributor with an average value of 215.66 ng/m3 followed by benzo[k]fluranthene with a concentration of 150.68 ng/m3, respectively. The major contributors were indeno[1,2,3-cd]pyrene, benzo[k]fluranthene, dibenzo[a,h]anthracene, benzo[g,h]perylene, and benzo[b]fluranthene are the major contributors with contributing percentages of 26.32, 18.39, 9.07, and 8.29%, respectively. The rest of all compounds were below 4%. The highest concentrations of PAHs in Obhur (1836.99 ng/m3) and in Hada Alsham (1107.40 ng/m3) were observed in winter in January 2014. PAHs with 4–6 aromatic ring components are primarily emitted by high temperature combustion. The average values for the BaA/(BaA + Chr) and Flt/(Flt + Pyr) ratios at Obhur were found 0.58 and 0.43 and at Hada Alsham were found 0.63 and 0.38, respectively, indicating that coal/biomass burning is the major source of PAHs. Hada Alsham (rural area), the transportation system, is a significant contributor to the observed PAHs. These results reflect Saudi Arabia’s traffic load in both rural and urban areas. On road sites, the impact of petroleum combustion and vehicular emissions was also identified. The sum of the incremental lifetime cancer risk (ILCR) for all congeners for infants along the Obhur location was 2.13 × 10−6 and 1.38 × 10−6, respectively. ILCR values were less than 1.0 × 10−4, implying that PAH exposure posed an acceptable potential cancer risk in this study. Various local emission sources contributed more PAHs in many Saudi urban areas, increasing the risk of lung cancer, and the health risk. PAHs have an associated large surface area and are capable of deposition in the respiratory system with high efficiency. The total health risk assessment study also helps in alarming the toxicity at both the locations.