Polycyclic Hydrocarbons Research Articles

Polycyclic aromatic hydrocarbons (PAHs) in crude oil-contaminated water and soil and their removal using locally available plant materials

ABSTRACT The presence of polycyclic aromatic hydrocarbons (PAHs) in water and soil can be harmful to human life when ingested. PAHs are determined in the water and soil of the B-Dere community of Rivers State, Nigeria. The extent of risk and source identification were carried out. The water samples were treated with garlic and Moringa seed extracts, while the soil samples were treated with garlic and Fenton oxidation reagents. PAHs were extracted before and after treatment. The gas chromatograph mass spectrometer analyses showed 13 PAHs in the water and 10 PAHs in thesoil. The highest concentration in water was recorded for benzo(ghi)perylene, with a mean value of 27.7 ± 0.25 ngL−1, while that of soil was recorded for benz(a)anthracene, with a mean value of 14.4 ± 0.631 ngkg−1. The source of PAHs in water was pyrogenic, while that of soil was petrogenic. Garlic extract removed 100% of benz(a)anthracene and benzo(b)fluorothane from the water, while Moringa removed 100% biphenylene from the water. However, garlic extract removed 2.59% of acenaphthylene, while Fenton reagents removed 100% of anthracene, phenathrene, and chrysene from the soil. Moringa seed and garlic extracts can be used in PAH's polluted water treatment.

Enhanced Remediation of Polycyclic Aromatic Hydrocarbons in Soil Through Fungal Delignification Strategy and Organic Waste Amendment: A Review

AbstractNutrient-limited soils from growing global contamination with polycyclic aromatic hydrocarbons (PAHs) and the massive organic waste generation from agro-based and food industries have raised more demand for exploring and recycling the latter as sustainable, cost-effective, and green nutrient-rich sources for soil amendment. To further enhanced the potentials of these substrates in soil, immobilisation or biological pre-treatment techniques using fungi are employed. The white-rot fungi- basidiomycetes, are the most widely researched and efficient organisms to perform these functions because of their high lignin-degrading ability for organic materials, such as corn cob, straws, spent brewery grains, sugarcane bagasse, etc. This review addresses the importance of organic amendment to enhance the biodegradation efficiency of PAH from contaminated soils and it also highlights various biological techniques for improving PAH biodegradation using organic waste materials and white-rot basidiomycetes. This review will also show a better understanding of the concepts of fungal immobilisation and pre-treatment for PAH degradation in soil and show their insights as feasible and optimise techniques for developing remedial strategies for contaminated soils.

Relationship between mixed exposure to phenyl hydroxides, polycyclic aromatic hydrocarbons, and phthalates and the risk of arthritis

BackgroundTo determine the relationship between mixed exposure to three types of endocrine-disrupting chemicals (EDCs), namely phenyl hydroxides, polycyclic aromatic hydrocarbons (PAHs), and phthalates (PAEs), and risk of arthritis.MethodsParticipants were selected from National Health and Nutrition Examination Survey (NHANES). The relationships between the urinary concentrations of phenyl hydroxides, PAHs, and PAEs and the risk of arthritis were analyzed by generalized linear regression model. The mixed exposure to these EDCs and the risk of arthritis was analyzed by weighted quantile sums (WQSs) and Bayesian kernel machine regression (BKMR) model.ResultsOur analysis showed that participants with urinary benzophenone-3 and methylparaben concentrations in the highest quartile (Q4) had an increased risk of arthritis compared with those in Q1. For each one-unit increase in the natural logarithm-converted urinary concentrations of 1-hydroxynapthalene and 2-hydroxynapthalene, the risk of arthritis increased by 5% and 8%, respectively. Chemical mixing index coefficients were significantly associated with risk of arthritis in both WQS positive- and negative-constraint models. In the BKMR model, there was a significant positive correlation between mixed exposure and the risk of arthritis.ConclusionMixed exposure to phenyl hydroxides, PAHs, and PAEs increased the risk of arthritis, with exposure to PAHs being the key factor.

Characterization of 2-phenanthroate:CoA ligase from the sulfate-reducing, phenanthrene-degrading enrichment culture TRIP.

Polycyclic aromatic hydrocarbons (PAHs) constitute a class of very toxic and persistent pollutants in the environment. However, the anaerobic degradation of three-ring PAHs such as phenanthrene is barely investigated. The initial degradation step starts with a carboxylation followed by a CoA‑thioesterification reaction performed by an aryl-CoA ligase. The formation of a CoA-thioester is an important step in the degradation pathway of aromatic compounds because the CoA-ester is needed for all downstream biochemical reactions in the pathway. Furthermore, we provide biochemical proof for the identification of the first genes for anaerobic phenanthrene degradation. Results presented here provide information about the biochemical and structural properties of the purified 2‑phenanthroate:CoA ligase and expand our knowledge of aryl-CoA ligases.

Small‐Molecule Polycyclic Aromatic Hydrocarbons as Exceptional Long‐Cycle‐Life Li‐Ion Battery Anode Materials

The growing demand for cost‐effective and sustainable energy‐storage solutions has spurred interest in novel anode materials for lithium‐ion batteries (LIBs). In this study, the potential of small‐molecule polycyclic aromatic hydrocarbons (SMPAHs) as promising candidates for LIB anodes is explored. Through a comprehensive experimental approach involving electrode fabrication, material characterization, and electrochemical testing, the electrochemical performance of SMPAHs, including naphthalene, biphenyl, 9,9‐dimethylfluorene, phenanthrene, p‐terphenyl, and pyrene (Py), is thoroughly investigated. In the results, the impressive cycle stability, high specific capacity, and excellent rate capability of the SMPAH electrode are revealed. Additionally, a direct contact prelithiation strategy is implemented to enhance the initial Coulombic efficiency (ICE) of SMPAH anodes, yielding significant improvements in the ICE and cycle stability. Computational simulations provide valuable insights into the electrochemical behavior and lithium‐storage mechanisms of SMPAHs, confirming their potential as effective anode materials. The simulations reveal favorable lithium adsorption sites, the predominant storage mechanisms, and the dissolution mechanism of Py through computational calculations. Overall, in this study, the promise of SMPAHs is highlighted as sustainable anode materials for LIBs, advancing energy‐storage technologies toward a greener future.

NaNbO3 Nanocubes: Perovskite Catalysts for Methanol Polymerization

Polyoxymethylene dimethyl ethers (PODEs) are a class of oxygenated fuels with promising applications in energy production and emission reduction. They are often utilized as a diesel fuel additive or substitute, which reduces the formation of harmful emissions such as polycyclic aromatic hydrocarbons (PAH), soot, nitrogen oxides (NOx), and carbon monoxide (CO). The oxidative polymerization of methanol presents a promising route for the formation of PODEs. NaNbO3, a type of perovskite oxide, was synthesized with a well-defined nanocubic structure through solvothermal synthesis using a Nb2O5 precursor. The catalytic potential of both the NaNbO3 nanocubes and the well-studied Nb2O5 precursor was assessed for the oxidative polymerization of methanol into PODEs. NaNbO­3 demonstrated catalytic performance comparable to Nb2O5 as both catalysts produced formaldehyde and dimethyl ether, which are precursors to PODE. Powder X-ray diffraction, scanning electron microscopy, transmission electron microscopy, x-ray photoelectron spectroscopy, and Brunauer-Emmett-Teller (BET) surface area confirmed the crystalline nature and desired cubic morphology of the NaNbO3 nanocubes. Additionally, Nb2O5 precursors with an orthorhombic, as opposed to a monoclinic or hexagonal crystal system were determined to produce NaNbO3 nanocubes successfully. Effective shape control of the NaNbO3 nanocubes makes this catalyst an intriguing material to understand and apply in heterogenous catalysis.

Quantitative filter forensics for allergens and semivolatile organic compounds in residential buildings in Toronto, Canada

Quantitative filter forensics (QFF) is a method for estimating the time-averaged concentration of particle-bound containments using filter metadata and its extracted dust. In this study, QFF was applied to dust samples extracted from four types of HVAC filters deployed in 20 homes from December 2016 to December 2017 in Toronto, Canada. The analysis covered six allergens, eight phthalates, and 12 polycyclic aromatic hydrocarbons (PAHs). The allergen results from four homes showed elevated concentrations of cat and dog allergens (Fel d 1 and Can f 1) in homes with cats or dogs. All eight phthalates were detected, dominated by diisononyl phthalate (DiNP) and bis(2-ethylhexyl) phthalate (DEHP), with median concentrations of 4.27 ng/m³ and 4.20 ng/m³, respectively. All PAHs, except anthracene, were detected in over 50 % of the homes, with benzo[a]pyrene being the most abundant (median concentration of 0.067 ng/m³). Median concentrations of all semivolatile organic compounds (SVOCs) were lower in winter 2016 compared to spring 2017, potentially due to losses of more volatile SVOCs from filters because of higher filtration volumes in winter, in addition to differences in sources and ventilation rates. All phthalate and most PAH concentrations were one to two orders of magnitude lower compared to those found from QFF in apartments in Toronto social housing multi-unit residential buildings (MURB), indicating those with lower socio-economic status (SES) were exposed to higher SVOC concentrations. Occupant density was positively related to most phthalate and specific PAH concentrations, while environmental factors including room temperature, relative humidity, and supply air temperature were not.

Screening of Characteristic Pollutants and Risk Pollutants in Different Media in the Yangtze River Basin Using Comprehensive Evaluation and Risk Quotient Methods

A variety of pollutants have frequently been detected in the Yangtze River Basin with the rapid economic development, the population increase, and the acceleration of urbanization, which threaten the aquatic ecosystem and human health. A multi-criteria comprehensive evaluation method was developed to identify the characteristic pollutants, and the risk quotient method was used to derive the risk pollutants in water and sediment samples in this article. A total of 155 pollutants from 11 categories were detected in the Yangtze River Basin according to the literature research. Then, the K-means method was used to analyze the cluster of pollutant comprehensive scores. All pollutants were graded based on their scores and recorded as Ⅰ-Ⅵ according to the number of cases in each cluster. A total of 43 pollutants with high scores of Ⅰ and Ⅱ were listed as the characteristic pollutants, which included 11 polycyclic aromatic hydrocarbons, 11 organochlorine pesticides, 10 polychlorinated biphenyls, eight dioxins, two heavy metals, and one phthalate ester. The top five median concentrations of contaminants in water and sediment samples were heavy metals, polycyclic aromatic hydrocarbons, phthalates esters, bisphenols, and pharmaceuticals and personal care products. According to the principle of risk maximization, the risk entropy value （RQ） was calculated based on the highest pollutant concentration. A total of 38 risky pollutants were screened in the water samples （RQ ≥ 0.1）. There were eight high-risk pollutants with RQ ≥ 1, which included benzo[a,h]-anthracene, anthracene, benzo[a]anthracene, pyrene, methoxychlor, aldrin, 2,4'-dichlorodiphenyl, and cadmium. There were 15 high-risk contaminants in the sediment, which included benzo[b]fluoranthene, anthracene, acenaphthene, fluoranthene, cadmium, lead, chromium, arsenic, selenium, dibutyl phthalate, dimethyl phthalate, diisobutyl phthalate, norfloxacin, perfluorobutyric acid, and bisphenol A. The risk pollutants contained emerging pollutants, which included ten pollutants in water samples and nine pollutants in sediments. Antibiotic pollutants accounted for the largest proportion of these emerging pollutants. The information provided in this article may be useful for the relevant departments to monitor the pollutants and propose management programs for the Yangtze River Basin. Additionally, it is of great significance for the ecological environmental protection and management of the Yangtze River Basin.

Levels, enrichment characteristics, and health risks of halogenated and parent polycyclic aromatic hydrocarbons in traditional smoked pork

Chinese traditional smoked pork was contaminated with polycyclic aromatic hydrocarbons (PAHs) and chlorinated and brominated PAHs (ClPAHs and BrPAHs; XPAHs) during the smoking process. Therefore, our study investigated the concentrations, enrichment characteristics, and health risks associated with PAHs, as well as ClPAHs and BrPAHs in Chinese traditional smoked pork. The total concentrations of PAHs, ClPAHs and BrPAHs in traditional smoked pork ranged from 90.0 to 79200 ng/g fat weight (fw), 23.6–2340 pg/g fw and 0.550–200 pg/g fw, respectively, which were significantly higher than their levels found in raw pork. Additionally, the concentrations of PAHs and XPAHs in the surface of smoked pork were higher than those in the inner parts. High-ring PAHs exhibited a greater enrichment compared to low-ring PAHs, and BrPAHs exhibited greater enrichment ability than ClPAHs in smoked pork. Furthermore, the ability of individual congeners to migrate from the surface to the inner parts of the smoked pork were varied. When the smoking fuels were similar, a longer smoking time resulted in higher concentrations of PAHs and XPAHs in smoked pork, while casing effectively reduced their concentrations. The correlation between XPAH and parent PAH concentrations indicated that chlorination of PAHs was one of the primary formation mechanisms of some monochlorinated PAHs. Over half of the smoked pork samples posed a potential carcinogenic risk, particularly the surface samples. It is recommended to remove the surface parts when consuming smoked pork and to improve traditional smoking methods to mitigate the health risks.

Naphthalene Enhances Polycyclic Aromatic Hydrocarbon Biodegradation by Pseudomonas aeruginosa in Soil and Water: Effect and Mechanism

Bioremediation is a promising technique owing to its effectiveness, low cost, and environmental friendliness. Previous studies have focused on the degradation efficiency of polycyclic aromatic hydrocarbons (PAHs) in soil and water. However, the expression of PAH-catabolic genes in organisms involved in the degradation process has been rarely and unsystematically reported. In this study, a PAH-degrading strain—Pseudomonas aeruginosa (PQ249631)—was successfully isolated from coking-contaminated soil and used for PAH degradation in soil and water. Furthermore, the degradation of PAHs (naphthalene, fluorene, phenanthrene, anthracene, and pyrene) was investigated in single, binary, and mixture systems to explore the interaction of substrates. The results showed that when naphthalene was used as a cometabolite carbon source, the removal rates of fluorene, phenanthrene, anthracene, and pyrene increased from 14.33%, 17.25%, 6.61%, and 4.47% to 72.08%, 100.00%, 15.63%, and 6.63%, respectively. In a PAH mixture, the degradation rate of each PAH was higher when naphthalene, rather than glucose, was used as the cometabolite carbon source. Transcriptome analysis revealed significant differential expression of PAH-catabolic genes and ATP-binding cassette transporter-related genes under naphthalene stress. The enhanced degradation of PAHs could be attributed to the augmentation of the PAH metabolic pathway and membrane transportation, facilitating the transfer of PAHs to bacteria. These findings underscore the effectiveness of P. aeruginosa as a PAH degrader and provide molecular insights into enhancing PAH degradation.

Preparation of sp2c-COF functionalized silica gel material as chromatographic stationary phases for their high-resolution separation of geometric isomers

Exploration and development of novel chromatographic stationary phases is an effective way to improve the separation efficiency of geometric isomers with similar physicochemical properties. Covalent organic frameworks (COFs) are a new class of porous organic polymers that show a wide range of applications in the field of separation science due to their tunable geometries and functionalities, infinitely extended network structures, and abundant interaction sites. However, the common imine-bonded COFs are poorly resistant to hydrolysis in HPLC. In this work, 2,4,6-trimethyl-1,3,5-triazine (TMT) and 1,3,5-tris (4-formylphenyl) triazine (TFPT) were used as raw materials, a sp2 carbon-conjugated covalent organic framework (sp2c-COF) was synthesized through self-assembly monolayer-assisted surface-initiated Schiff-base-mediated hydroxyl-aldehyde condensation reaction, and loaded on the surface of silica substrate with a CN bond to obtain a new segregated material (SiO2@sp2c-COF). SiO2@sp2c-COF was used as a high-performance liquid chromatography (HPLC) packing material for the separation of geometric isomers. Benefitting from its superb in-plane π-conjugation, highly ordered and robust framework structure, high chemical and thermal stability of sp2c-COF, and the unique hydrophilic covalent triazine groups, hydrophobic benzene rings and other groups that can provide a variety of interactions such as hydrophobicity, π-π stacking, hydrogen bonding and hydrophilicity of the prepared SiO2@sp2c-COF stationary phases, they exhibit excellent molecular shape selectivity and resolution in separating geometrical isomers. These geometric isomers include isomers such as polycyclic aromatic hydrocarbons (PAHs), tocopherols, carotenoids, diethylstilbestrol, 1,4-cyclohexanediol and astaxanthin. Compared to commercial C18 columns, this column has more flexible selectivity and higher separation performance. In addition, due to the introduction of hydrophobicity, π-π stacking action and hydrophilic triazine components, the SiO2@sp2c-COF stationary phase also has RPLC/HILIC mixed mode characteristics. Baseline separations of monosubstituted benzenes, alkylbenzenes, positional isomers, sulfonamides, benzoic acid, anilines, nucleosides and nucleobases compounds were achieved on SiO2@sp2c-COF packed columns. This successful application highlights the great potential of sp2c-COF for the separation of geometrical isomers, and provides a way to overcome the stability of common imine-bonded COFs materials in HPLC, as well as to compensate for the shortcomings and deficiencies of a single chromatographic mode in the separation of complex samples. Furthermore, this is the first report of a practical separation of important geometrical isomers using sp2c-COF materials.

Pyrolysis characteristics and hydrogen production mechanism of biomass impregnated with transition metals

The application of metal impregnation pretreatment to improve the quality of biomass pyrolysis gas production is considered as a promising upgrading technology. Transition metals have been well developed for the unique structural characteristics. After impregnation pretreatment, the product distribution of biomass pyrolysis was changed, and the transfer path of H atoms and the formation mechanism of H2 can be revealed through analysis. The effects of impregnation pretreatment with three different transition metals (iron, cobalt, and nickel) on the pyrolysis characteristics of corn straw were evaluated in this work. Three transition metal solutions with concentrations of 0.5 M, 1 M, and 2 M were used to explore the influence of impregnation concentration on the yield and composition of the pyrolysis products. The results showed that iron promoted the formation of liquid products, whose proportion increased by 37.29% upon increasing the impregnation solution concentration. The addition of cobalt and nickel led to more pyrolysis gas generation. When the impregnation solution concentration was greater than 0.5 M, the gas production rate exceeded 45 wt%. Nickel simultaneously promoted the generation of H2 and CH4 in pyrolysis gas, whose yields were increased by 63% and 20% respectively compared with raw materials. Py-GC/MS analysis showed that Co-CS had strong decarboxylation characteristics during pyrolysis. Metal impregnation decreased the content of aromatic compounds in tar, which increased the stretching vibrations of C-H bonds in char. Ring-opening rearrangements of polycyclic aromatic hydrocarbons were promoted, which formed more -H. Nickel catalyzed the removal of CH3 and H groups and the rearrangement of C-O in volatile products, which formed more H2 and CH4. These findings provide an avenue to optimize the metal impregnation conditions to produce hydrogen via biomass pyrolysis.

Prenatal exposure to environmentally relevant levels of PAHs inhibits spermatogenesis in adult mice and the mechanism involved

Polycyclic aromatic hydrocarbons (PAHs) are a class of contaminants that cannot be banned. Exposure to PAHs has been reported to alter spermatogenesis in mammals, but little is known about prenatal exposure to a mixture of PAHs on the reproductive toxicity of adult offspring. In this study, we investigated the associations between prenatal exposure to environmentally relevant levels of PAHs in mice and testicular dysfunction, including impaired spermatogenesis and steroid hormone dysfunction in male offspring on postnatal day 180. The percentage of testicular apoptotic cells was significantly increased, which was further verified by the up-regulated BAX protein. The expression of Ar and the Leydig cell marker Cyp11a1 was down-regulated, suggesting an impairment in the synthesis of steroid hormones. DNA hypermethylation of the Tnp1 and Sohlh2 promoters suppresses transcriptional expression, consequently altering the sperm production process. This study shows that prenatal exposure to PAHs may induce long-term reproductive toxicity.

Plant Defense Mechanisms against Polycyclic Aromatic Hydrocarbon Contamination: Insights into the Role of Extracellular Vesicles.

Polycyclic aromatic hydrocarbons (PAHs) are persistent organic pollutants that pose significant environmental and health risks. These compounds originate from both natural phenomena, such as volcanic activity and wildfires, and anthropogenic sources, including vehicular emissions, industrial processes, and fossil fuel combustion. Their classification as carcinogenic, mutagenic, and teratogenic substances link them to various cancers and health disorders. PAHs are categorized into low-molecular-weight (LMW) and high-molecular-weight (HMW) groups, with HMW PAHs exhibiting greater resistance to degradation and a tendency to accumulate in sediments and biological tissues. Soil serves as a primary reservoir for PAHs, particularly in areas of high emissions, creating substantial risks through ingestion, dermal contact, and inhalation. Coastal and aquatic ecosystems are especially vulnerable due to concentrated human activities, with PAH persistence disrupting microbial communities, inhibiting plant growth, and altering ecosystem functions, potentially leading to biodiversity loss. In plants, PAH contamination manifests as a form of abiotic stress, inducing oxidative stress, cellular damage, and growth inhibition. Plants respond by activating antioxidant defenses and stress-related pathways. A notable aspect of plant defense mechanisms involves plant-derived extracellular vesicles (PDEVs), which are membrane-bound nanoparticles released by plant cells. These PDEVs play a crucial role in enhancing plant resistance to PAHs by facilitating intercellular communication and coordinating defense responses. The interaction between PAHs and PDEVs, while not fully elucidated, suggests a complex interplay of cellular defense mechanisms. PDEVs may contribute to PAH detoxification through pollutant sequestration or by delivering enzymes capable of PAH degradation. Studying PDEVs provides valuable insights into plant stress resilience mechanisms and offers potential new strategies for mitigating PAH-induced stress in plants and ecosystems.

Size-segregated content of heavy metals and polycyclic aromatic hydrocarbons in airborne particles emitted by indoor sources

Indoor air quality is negatively affected by the emission of different combustion sources releasing airborne particles and related particle-bound toxic compounds (e.g., heavy metals and polycyclic aromatic hydrocarbons). To date, very few studies focused on the chemical characterization of the airborne particles emitted by indoor sources were carried out; moreover, no data on their size-resolved chemical compositions are available. In the present study, an experimental analysis aimed at determining the size-segregated content of heavy metals and polycyclic aromatic hydrocarbons in airborne particles (including sub-micrometric ones) emitted by widely-used indoor combustion sources (i.e., incenses, candles, mosquito-coils, and cooking activities) was carried out. To this purpose, airborne particles were collected through an electric low-pressure impactor and were post-analyzed by means of chromatography–mass spectrometry and atomic emission spectrometry techniques. Results of the analyses showed that the chemical composition of the emitted particles is not invariant to the particle size, indeed, an important contribution of sub-micrometric particle range to the total mass of chemical compounds emitted by the sources was noticed. These findings also demonstrated that significant underestimations of particle-bound compounds depositing in the lungs could occur if size-dependent compositions are not adopted.

Perylene with Split‐Azulene Embedding

AbstractSplitting the five and seven‐membered rings of azulene and embedding them separately into a conjugated backbone provides azulene‐like polycyclic aromatic hydrocarbons (PAHs), which are of great interest in quantum and material chemistry. However, the synthetic accessibility poses a significant challenge. In this study, we present the synthesis of a novel azulene‐like PAH, Pery‐57, which can be viewed as the integration of a perylene framework into the split azulene. The compact structure of Pery‐57 displays several intriguing characteristics, including NIR II absorption at 1200 nm, a substantial dipole moment of 3.5 D, and head‐to‐tail alternating columnar packing. Furthermore, Pery‐57 exhibits remarkable redox properties. The cationic radical Pery‐57⋅+ readily captures a hydrogen atom. Variable‐temperature NMR (VT NMR ) and variable‐temperature EPR (VT‐EPR) studies reveal that the dianion Pery‐572− possesses an open‐shell singlet ground state and demonstrates significant global anti‐aromaticity. The dication Pery‐572+ is also predicted to exhibit diradical character. Despite bearing three bulky substituents, Pery‐57 displays p‐type transport characteristics with a mobility of 0.03 cm2 V−1 s−1, attributed to its unique azulene‐like structure. Overall, this work directs interest in azulene‐like PAHs, a unique member of nonalternant PAHs showcasing exceptional properties and applications.

Characterization of carbonaceous components and PAHs on ultrafine particles in Phnom Penh, Cambodia.

This study investigated seasonal fluctuations in particulate matter (PM) concentrations, including carbon and polycyclic aromatic hydrocarbon (PAH) components, in Phnom Penh, Cambodia, focusing on ultrafine particles (UFPs or ≤ 100nm). UFP levels were notably higher during the dry season, averaging 23.73 ± 3.7µg/m3 compared to 19.64 ± 3.4µg/m3 in the wet season, attributed to increased emissions from vehicles and agricultural burning. In contrast, lower concentrations during the wet season were due to scavenging effect of rain. When compared to other Southeast Asian cities, UFP levels in Phnom Penh were significantly higher during the dry season, surpassing those in cities like Bangkok and Kuala Lumpur. Seasonal variations in carbonaceous components showed higher elemental carbon (EC) and total carbon (TC) during the dry season, with EC/TC ratios suggesting substantial influence from vehicular emissions and biomass burning. PAH analysis revealed seasonal disparities, with higher concentrations of benzo[b]fluoranthene (BbF) and benzo[k]fluoranthene (BkF) during the wet season, whereas fluoranthene (Flu) and pyrene (Pyr) were consistently present, indicating diverse PAH sources. The Flu/(Flu + Pyr) ratios, indicative of biomass burning, were higher in the dry season. Correlations between PAHs and carbon components confirmed combustion as a significant source of PAHs, aligning with global trends. This emphasizes the need to address distinct PM sources during various season in Phnom Penh.

Polycyclic Aromatic Hydrocarbons (PAHs) Contamination Levels in Some Commercial Olive Oils Sold on the Markets in Giresun, Türkiye

Olive oil is widely consumed worldwide and well-known for its health beneficial effects. However, polycyclic aromatic hydrocarbons (PAHs) contamination in olive oils has been a serious concern and knowledge regarding PAH concentrations in olive oils is scarce. The aim of this study was the determination and evaluation of PAH contamination levels in olive oils in the market. In this study, commercial olive oils (n=14) available in the markets of Giresun (Türkiye), including extra virgin and riviera olive oil samples, were investigated. Samples were analyzed by a gas chromatography unit coupled with a mass spectrometer. Significant amounts of PAHs were determined in all olive oil samples. The PAH contents of the samples varied between 0.04 µg kg-1 and 4637.13 µg kg-1 with the mean content of 264.61 µg kg-1. Regarding benzo[a]pyrene, 64.28% of the samples was incompatible with the EU requirements. None of the samples were compatible with the EU requirements in terms of PAH4 components (benzo[a]pyrene, benzo(a)anthracene, chrysene, and benzo[b]fluoranthene). Results showed that commercial olive oils studied in this research might contain PAHs categorized under potential carcinogens.

QSPR-based prediction model for the melting point of polycyclic aromatic hydrocarbons using MLR and ANN methods

The melting point is an important property that helps generate specific compounds with desired thermos-physical properties. Much work has been done applying quantitative structure-property relationships to improve the melting-point correlations, but they are unreliable. This gap might come from the melting point's sensitivity for small molecular variations and descriptors, which currently do not fully consider all factors determining melting behavior. In this work, we provide a QSPR model for predicting the melting point of a heterogeneous polycyclic aromatic hydrocarbons dataset. The model was generated using a robust hybrid linear approach (Genetic Algorithm-Multiple Linear Regression) and a nonlinear approach named Artificial Neural Network (ANN). Three descriptors were chosen to explain the influence of molecular weight and symmetry on melting point. The resulting QSPR model can model melting-point behavior with an RMSE of 34.88K, a coefficient correlation value of R²=0.887, and a prediction coefficient of Q²LOO= 0.863. This study reveals that the results produced by MLR were appropriate and served to predict melting points. However, compared to the results obtained by the ANN model, we conclude that the latter is more effective and better than the MLR model. Based on the results, our suggested model may be effective in predicting melting points, and the selected descriptors play essential roles in determining melting points.

Evaluation of a self-monitoring protocol for assessing soot and polycyclic aromatic hydrocarbon exposure among chimney sweeps.

Traditional methods for measuring chemical exposure have challenges in terms of obtaining sufficient data; therefore, improved methods for better assessing occupational exposure are needed. One possible approach to mitigate these challenges is to use self-monitoring methods such as sensors, diaries, or biomarkers. In the present study, a self-monitored method for measuring soot exposure, which included real-time air monitoring, a work diary, and the collection of urine samples, was evaluated. To validate the method, exposure measurements during the workday and diary entries were compared with velocities calculated from GPS tracking and the expected polycyclic aromatic hydrocarbon (PAH) metabolite patterns in urine. The method was applied with chimney sweeps, an occupational group at a high risk of many severe health outcomes and for whom effective control measures for reducing exposure are needed. In the study, 20 chimney sweeps followed a self-monitoring protocol for 8 consecutive workdays. Personal exposure to soot was measured as black carbon (BC) using micro-aethalometers. A diary was used to record the work tasks performed, and urine samples were collected and analysed for PAH metabolites. From the expected 160 full day measurements, 146 (91%) BC measurements and 149 (93%) diaries were collected. From the expected 320 urine samples, 304 (95%) were collected. The tasks noted in the diaries overlapped with information obtained from the GPS tracking of the chimney sweeps, which covered 96% of the measurement time. The PAH metabolites in urine increased during the work week. Factors believed to have positively influenced the sample collection and task documentation were the highly motivated participants and the continuous presence of trained occupational hygiene professionals during the planning of the study and throughout the measurement stage, during which they were available to inform, instruct, and address questions. In conclusion, the self-monitored protocol used in this study with chimney sweeps is a valuable and valid method that can be used to collect larger numbers of samples. This is especially valuable for occupations in which the employees are working independently and the exposure is difficult to monitor with traditional occupational hygiene methods.