Search Results (16)

Polycyclic aromatic hydrocarbon (PAH) derivatives, specifically azaarenes and nitrated and oxygenated PAHs, are emerging contaminants of concern due to their increased toxicity and persistence compared to the parent PAHs. Despite their toxicity, their simultaneous analysis in complex matrices, such as in fumes emitted from bituminous mixtures, remains challenging due to limitations of conventional analytical techniques. To address this, an advanced methodology was developed using Ultra-High-Performance Liquid Chromatography coupled with High-Resolution Mass Spectrometry (UHPLC-HRMS Orbitrap Eclipse) equipped with an APCI source for the simultaneous identification and quantification of 14 PAH derivatives. Chromatographic and ionization parameters were optimized to ensure maximum sensitivity and selectivity. Following ICH Q2(R2) guidelines, the method was validated, demonstrating excellent linearity (R² > 0.99), high mass accuracy (≤5 ppm), strong precision (<15%), and excellent sensitivity. Limits of detection (LODs) ranged from 0.1 µg L⁻¹ to 0.6 µg L⁻¹ and limits of quantification (LOQs) ranged from 0.26 µg L⁻¹ to 1.87 µg L⁻¹. The validated method was successfully applied to emissions from asphalt pavement materials collected on quartz filters under controlled conditions, enabling the identification and quantification of all 14 targeted compounds. These results confirm the method’s robustness and suitability for trace-level analysis of PAH derivatives in complex environmental matrices. Full article

Increasing urbanization and the associated sealing of areas and the use of storm sewer systems for drainage not only increase the risk of flooding but also reduce water quality in streams into which stormwater is discharged. Green infrastructure (GI) measures are applied with the aim of managing this stormwater sustainably and reducing the associated risks. To this end, a quantitative–qualitative approach was developed to simulate GI—namely, rain gardens, bioretention cells, and vegetative bioswales—at the urban catchment scale. The findings highlight the potential of applying GI measures to managing stormwater more effectively in urban environments and mitigating its negative pollution-related impacts. For the housing estate analyzed, a simulated implementation of GI resulted in a reduction in pollution, measured as total nitrogen (N; 9–52%), nitrate-N (5–30%), total phosphorus (11–59%), chemical oxygen demand (8–46%), total suspended solids (13–73%), copper (12–64%), zinc (Zn; 16–87%), polycyclic aromatic hydrocarbons (16–91%), and the hydrocarbon oil index (HOI; 15–85%). Reducing the concentrations of pollutants minimizes the risk to human health determined via the HOI from a low-risk level to zero risk and reduces the ecological risk in terms of Zn pollution from a significant risk to a low risk of adverse effects. The modeling conducted clearly shows that the GI solutions implemented facilitated a quantitative reduction and a qualitative improvement in stormwater, which is crucial from an environmental perspective and ensures a sustainable approach to stormwater management. Lowering the levels of stormwater pollution through the implementation of GI will consequently lower the environmental burden of pollutants in urban areas. Full article

Stormwater runoff from large roads is a major source of pollutants to receiving waters, and reduction of these pollutants is important for sustainable water resources and transportation networks. Porous pavements have been shown to substantially reduce many of these pollutants, but studies are lacking on arterial roads. We sampled typical stormwater pollutants in runoff from sections of an arterial road 9–16 years after installation of three pavement types: control with conventional asphalt, porous asphalt overly, and full-depth porous asphalt. Both types of porous pavements substantially reduced most of the stormwater pollutants measured. Total suspended solids, turbidity, total lead, total copper, and 6PPD-quinone were all reduced by >75%. Total nitrogen, ammonia, total phosphorus, biochemical oxygen demand, total and dissolved copper, total mercury, total zinc, total polycyclic aromatic hydrocarbons, and di-2-ethylhexyl phthalate were all reduced by >50%. Reductions were lower or absent for nitrate, orthophosphate, E. coli, dissolved lead, and dissolved zinc. Most reductions were statistically significant. Many pollutants exceeded applicable water quality standards in the control samples but met them with both types of porous pavement. This study demonstrates that porous overlays and full-depth porous asphalt can provide substantial reductions of several priority stormwater pollutants on arterial roads for many years after installation. Porous pavements have the potential to substantially enhance water quality of urban waterways and provide ecological benefits on urban thoroughfares. Full article

Fine particles (PM_2.5) have generally been reported as the major contributor to the adverse health effects of air pollution. Lebanon is characterized by a high density of transport, the production of electricity by generators, and a problem of uncontrolled incineration of household waste. For the purpose of this paper, the physico-chemical properties of fine (PM_2.5-0.3) and quasi-ultrafine (PM_0.3) particulate matter sampled in Southern Lebanon, were studied. Then, an evaluation and comparison of the toxicity of the different extracted fractions from PM (i.e., native PM_2.5-0.3 vs. organic extractable matter fraction (OEM_2.5-0.3), and non-extractable matter fraction (NEM_2.5-0.3)) was performed. Also, an examination of the toxicity of PM_0.3 was conducted indirectly through the evaluation of the OEM_0.3 harmfulness. The physico-chemical analysis showed that PM_0.3 was much more concentrated than PM_2.5-0.3 in organic compounds such as polycyclic aromatic hydrocarbons (PAHs) (28-fold) and their nitrated (N-PAHs, 14-fold) and oxygenated (O-PAHs, 10-fold) derivatives. Normal human bronchial epithelial cells (BEAS-2B) were exposed to PM_2.5-0.3, its derived fractions (i.e., OEM_2.5-0.3 and NEM_2.5-0.3), and OEM_0.3 before evaluating the global cytotoxicity, metabolic activation of organic compounds, genotoxicity, and inflammatory response. Different responses were observed depending on the considered fraction of particles. The global cytotoxicity showed a pronounced response related to ATP and LDH activities after exposure to the quasi-ultrafine organic extractable matter fraction (OEM_0.3). There was no significant induction of the AhR cell-signaling pathway by NEM_2.5-0.3. Despite the apparent difference in the kinetics of induction of the toxicological endpoints under study, OEM_0.3 provoked a higher overall cytotoxicity and genotoxicity than OEM_2.5-0.3 and total PM_2.5-0.3. Taken together, these results clearly showed that the finest particles are more damaging to BEAS-2B cells than PM_2.5-0.3 because they are richer in organic compounds, thereby inducing more remarkable toxic effects. Full article

To understand the influences of emulsified fuel on ship exhaust emissions more comprehensively, the emissions of particulate matter (PM), nitrated, oxygenated and parent polycyclic aromatic hydrocarbons (PAHs) were studied on a ship main engine burning emulsified heavy fuel oil (EHFO) and heavy fuel oil (HFO) as a reference. The results demonstrate that EHFO (emulsified heavy fuel oil) exhibits notable abilities to significantly reduce emissions of particulate matter (PM) and low molecular weight PAHs (polycyclic aromatic hydrocarbons) in the gas phase, particularly showcasing maximum reductions of 13.99% and 40.5%, respectively. Nevertheless, burning EHFO could increase the emission of high molecular weight PAHs in fine particles and pose a consequent higher carcinogenic risk for individual particles. The total average (gaseous plus particulate) ΣBEQ of EHFO exhausts (41.5 μg/m³) was generally higher than that of HFO exhausts (18.7 μg/m³). Additionally, the combustion of EHFO (extra-heavy fuel oil) can significantly alter the emission quantity, composition, and particle-size distribution of PAH derivatives. These changes may be linked to molecular structures, such as zigzag configurations in C=O bonds. Our findings may favor the comprehensive environmental assessments on the onboard application of EHFO. Full article

Coke production is an important source of environmental polycyclic aromatic compounds (PACs), including parent polycyclic aromatic hydrocarbons (PAHs) and their derivatives. The focus near coking plants has primarily been on parent-PAH contamination, with less attention given to highly toxic derivatives. In this study, soil samples were collected from both within and outside of a coking plant. The concentrations of parent-PAHs and their derivatives, including methylated-PAHs, oxygenated-PAHs, and nitrated-PAHs, were examined. Spatial interpolation was employed to determine their spatial distribution patterns. Methods for identifying potential sources and conducting incremental lifetime cancer risk analysis were used. This could achieve a comprehensive understanding of the status of PAC pollution and the associated health risks caused by coke production. The concentrations of total PACs inside the plant ranged from 7.4 to 115.8 mg/kg, higher than those outside (in the range of 0.2 to 65.7 mg/kg). The spatial distribution of parent-PAH concentration and their derivatives consistently decreased with increasing distance from the plant. A significant positive correlation (p < 0.05) among parent-PAHs and their derivatives was observed, indicating relatively consistent sources. Based on diagnostic ratios, the potential emission sources of soil PACs could be attributed to coal combustion and vehicle emissions, while principal component analysis–multiple linear regression further indicated that primary emissions and secondary formation jointly influenced the PAC content, accounting for 60.4% and 39.6%, respectively. The exposure risk of soil PACs was dominated by 16 priority control PAHs; the non-priority PAHs’ contribution to the exposure risk was only 6.4%. Full article

Polycyclic aromatic hydrocarbons (PAHs) and their derivatives have received extensive attention due to their negative effects on the environment and on human health. However, few studies have performed comprehensive assessments of PAHs emitted from pesticide factories. This study assessed the concentration, composition, and health risk of 52 PM_2.5-bound PAHs during the daytime and nighttime in the vicinity of a typical pesticide factory. The total concentration of 52 PAHs (Σ52PAHs) ranged from 53.04 to 663.55 ng/m³. No significant differences were observed between daytime and nighttime PAH concentrations. The average concentrations of twenty-two parent PAHs, seven alkylated PAHs, ten oxygenated PAHs, and twelve nitrated PAHs were 112.55 ± 89.69, 18.05 ± 13.76, 66.13 ± 54.79, and 3.90 ± 2.24 ng/m³, respectively. A higher proportion of high-molecular-weight (4–5 rings) PAHs than low-molecular-weight (2–3 rings) PAHs was observed. This was likely due to the high-temperature combustion of fuels. Analysis of diagnostic ratios indicated that the PAHs were likely derived from coal combustion and mixed sources. The total carcinogenic equivalent toxicity ranged from 15.93 to 181.27 ng/m³. The incremental lifetime cancer risk from inhalation, ingestion, and dermal contact with the PAHs was 2.33 × 10⁻³ for men and 2.53 × 10⁻³ for women, and the loss of life expectancy due to the PAHs was 11,915 min (about 0.023 year) for men and 12,952 min (about 0.025 year) for women. These results suggest that long-term exposure to PM_2.5 emissions from a pesticide factory has significant adverse effects on health. The study results support implementing the characterization of PAH emissions from pesticide factories and provides a scientific basis for optimizing the living environment around pesticide factories. Full article

In this work, a novel analytical methodology for the extraction and determination of polycyclic aromatic hydrocarbon derivatives, nitrated (NPAH) and oxygenated (OPAH), in bee honey samples was developed. The extraction approach resulted in being straightforward, sustainable, and low-cost. It was based on a salting-out assisted liquid-liquid extraction followed by liquid chromatography-tandem mass spectrometry determination (SALLE-UHPLC-(+)APCI-MS/MS). The following figures of merit were obtained, linearity between 0.8 and 500 ng g⁻¹ for NPAH and between 0.1 and 750 ng g⁻¹ for OPAH compounds, coefficients of determination (r2) from 0.97 to 0.99. Limits of detection (LOD) were from 0.26 to 7.42 ng g⁻¹ for NPAH compounds and from 0.04 to 9.77 ng g⁻¹ for OPAH compounds. Recoveries ranged from 90.6% to 100.1%, and relative standard deviations (RSD) were lower than 8.9%. The green assessment of the method was calculated. Thus, the Green Certificate allowed a classification of 87 points. This methodology was reliable and suitable for application in honey samples. The results demonstrated that the levels of nitro- and oxy-PAHs were higher than those reported for unsubstituted PAHs. In this sense, the production chain sometimes transforms foods as direct carriers of contaminants to consumers, representing a concern and demonstrating the need for routine control. Full article

Anaerobic ammonium oxidation (anammox) has shown success in past years for the treatment of municipal and industrial wastewater containing inorganic nutrients (i.e., nitrogen). However, the increase in polycyclic aromatic hydrocarbon (PAH)-contaminated matrices calls for new strategies for efficient and environmentally sustainable remediation. Therefore, the present review examined the literature on the connection between the anammox process and PAHs using VOSviewer to shed light on the mechanisms involved during PAH biodegradation and the key factors affecting anammox bacteria. The scientific literature thoroughly discussed here shows that PAHs can be involved in nitrogen removal by acting as electron donors, and their presence does not adversely affect the anammox bacteria. Anammox activity can be improved by regulating the operating parameters (e.g., organic load, dissolved oxygen, carbon-to-nitrogen ratio) and external supplementation (i.e., calcium nitrate) that promote changes in the microbial community (e.g., Candidatus Jettenia), favoring PAH degradation. The onset of a synergistic dissimilatory nitrate reduction to ammonium and partial denitrification can be beneficial for PAH and nitrogen removal. Full article

The genotoxicity, mutagenesis, and carcinogenic effects of polycyclic aromatic hydrocarbon (PAH) derivatives may exceed the parent PAHs. However, their influence on the soil environment has not been explored to a large extent. Oxygenated polycyclic aromatic hydrocarbons (OPAHs) and nitrated polycyclic aromatic hydrocarbons (NPAHs) are typical polar substituted compounds. We offer a review of the literature on the sources, quantification, incidence, toxicity, and transport of these compounds in soil. Although their environmental concentrations are lower than those of their parent compounds, they exert higher toxicity. Both types of substances are basically related to carcinogenesis. OPAHs are not enzymatically activated and can generate reactive oxygen species in biological cells, while NPAHs have been shown to be mutagenic, genotoxic, and cytotoxic. These compounds are largely derived from the transformation of PAHs, but they behave differently in soil because of their higher molecular weight and dissimilar adsorption mechanisms. Therefore, specialized knowledge of model derivatives is required. We also made recommendations for future directions based on existing research. It is expected that the review will trigger scientific discussions and provide a research basis for further study on PAH derivatives in the soil environment. Full article

To establish the risk of the endocrine disrupting activity of polycyclic aromatic compounds, especially oxygenated and nitrated polycyclic aromatic hydrocarbons (oxy-PAHs and nitro-PAHs, respectively), antiandrogenic and estrogenic activities were determined using chemically activated luciferase expression (CALUX) assays with human osteoblast sarcoma cells. A total of 27 compounds including 9 oxy-PAHs (polycyclic aromatic ketones and quinones) and 8 nitro-PAHs was studied. The oxy-PAHs of 7H-benz[de]anthracen-7-one (BAO), 11H-benzo[a]fluoren-11-one (B[a]FO), 11H-benzo[b]fluoren-11-one (B[b]FO), and phenanthrenequinone (PhQ) exhibited significantly the potent inhibition of AR activation. All nitro-PAHs exhibited high antiandrogenic activities (especially high for 3-nitrofluoranthene (3-NFA) and 3-nitro-7H-benz[de]anthracen-7-one (3-NBAO)), and the AR inhibition was confirmed as noncompetitive for 3-NFA, 3-NBAO, and 1,3-dinitropyrene (1,3-DNPy). Antiandrogenic activity of 3-NFA demonstrated characteristically a U-shaped dose–response curve; however, the absence of fluorescence effect on the activity was confirmed. The prominent estrogenic activity dependent on dose–response curve was confirmed for 2 oxy-PAHs (i.e., B[a]FO and B[b]FO). Elucidating the role of AR and ER on the effects of polycyclic aromatic compounds (e.g., oxy- and nitro-PAHs) to endocrine dysfunctions in mammals and aquatic organisms remains a challenge. Full article

Polycyclic aromatic hydrocarbons (PAHs) are present in smoked food products. More toxic nitrated (NPAH) and oxygenated (OPAH) PAHs derivatives are found concomitantly to PAHs and are therefore believed to be found in smoked food products. However, only a few PAH analyses on food include these derivatives. We adjusted and successfully validated a GC-QTOFMS method including 13 NPAHs and 2 OPAHs as well as the 4 regulated PAHs for analysis of 14 smoked (13 fish and one bacon) and one pan fried fish samples.OPAHs were detected in the highest concentrations in 13 of 15 samples. Non-target screening revealed the presence of an additional four OPAHs and two methylated PAHs. Future food analysis should, based on these results, focus on PAH and oxygenated derivatives. Full article

Exhaust emissions from vehicles are the subject of numerous studies and legal acts. In the European Union, exhaust emissions are regulated by “Euro” emission standards, which limit emissions of gaseous pollutants such as CO, CO₂, HC, and NOx, as well as the particulate matter (PM) and particle number (PN). Solid particles consist of a number of micro-contaminants, inter alia polycyclic aromatic hydrocarbons (PAHs) and their nitrated and oxygenated derivatives. Despite their highly mutagenic and carcinogenic character, these micro-contaminants are not regulated in Euro emissions standards. This paper presents both a general discussion of the phenomenon of particulate formation in and emission from direct injection gasoline engines, as well as a wide range of results on the subject. The subject of the micro-contaminants in solid particles from modern gasoline vehicles is explored. The samples of solid particles were collected from 11 groups of vehicles according to the WLTP test methodology. Solid particles from gasoline vehicles were analyzed via various analytical techniques, including ion chromatography (IC) to measure selected anion concentrations, gas chromatography with mass spectroscopy (GC-MS) to study 16 PAHs and selected PAH derivatives, scanning electron microscopy with energy-dispersive spectroscopy (SEM/EDS) for images and elemental composition, and microwave plasma atomic emission spectroscopy (MP-AES) for qualitative screening analysis of 19 elements. The study of non-regulated compounds is crucial in efforts to establish the influence of solid particles on health and the environment. Furthermore, extended studies can provide a basis for further research on vehicle emissions or other fields, such as medicine or material engineering. Full article

Long-term wastewater and reclaimed water irrigation systems constitute the major processes in local water circulation, which concomitantly introduce plenty of undesirable substances that can threaten water quality, ecosystem functions and human health. At the Southeast Reclaimed Water Irrigation Region (SRWIR) of Beijing, wastewater irrigation was adopted from 1969 to 2002, and second-treated effluents (reclaimed water) has been used thereafter. Polycyclic aromatic hydrocarbons (PAHs) were the most ubiquitously detected contaminant in wastewater and reclaimed water and are reported to be carcinogenic. Hence, we measured the concentrations of dissolved sixteen United States Environmental Protection Agency (USEPA) priority PAHs in surface water and groundwater at the SRWIR to characterize their spatial and temporal variations, and to clarify the role of reclaimed water to natural water. The concentration of 16 individual PAHs in reclaimed water, rivers and groundwater varied from 339.4 to 636.2 ng/L, 359.1 to 3,435.0 ng/L and 216.5 to 488,205.2 ng/L, respectively. The lower aromatic rings of PAHs prevailed in aquatic environments rather than the higher ones. Thereinto, naphthalene was the predominant isomer within the highest concentration reached to 486,600 µg/L. The groundwater samples had higher PAHs concentrations at Tongzhou district which attributed to the higher vulnerability of aquifer. Additionally, strong correlations between PAHs and total nitrogen, nitrate, dissolved oxygen and electrical conductivity suggested those potential factors affecting the photo degradation and/or biodegradation of PAHs. The relationship identified between PAHs concentrations and physical and chemical indices would help us to enhance the understanding migration and transformation of PAHs spatially and temporally, enable us to assess the potential risks of the environmental pollutants to aquatic organisms and human water supplies. Full article

In this study, we analyzed the impacts of different environmental conditions on aquatic worm communities along the Danube River, based on two longitudinal surveys, the Joint Danube Surveys 2 and 3 (JDS; 2007 and 2013). We identified the most important environmental factors (among analyzed groups) that shape worm communities: hydromorphlogical alterations, flow velocity and substrate (HYMO group), dissolved oxygen, nitrates and nitrites (physico-chemical parameters), zinc and nickel (metals), monobutyltin cation, benzo(b) fluoranthene and benzo(k)fluoranthene, polychlorinated biphenyls PCB 77 and PCB 118 (selected chemical determinants—organotin compounds, Polycyclic aromatic hydrocarbons—PAHs and PCBs). A homogenization of species composition of Oligochaeta assemblages along the Danube was confirmed. As one of main factors related to biotic homogenization, hydromorphological alterations represented by similar changes in flow velocity and substrates along Danube’s course could be singled out. Our results indicate that Oligochaeta could be used for the identification of the level of hydromorphological degradation in large rivers (homogenization), rather than for stressors classified as nutrient and organic pollutants. Our results provide additional evidence in risk assessment of the environment, contributing in water management and monitoring of the ecological status as proposed by the Water Framework Directive. Full article