Polycyclic Aromatic Hydrocarbons Pollution Research Articles

Influence mechanisms of dissolved organic matter and iron minerals on naphthalene attenuation during river infiltration

Natural attenuation of naphthalene (NAP) in riverbank filtration zones is vital for maintaining water quality and is affected by dissolved organic matter (DOM) and iron minerals. However, the effects of DOM and iron minerals on the attenuation of NAP remain unclear. In this study, the attenuation mechanisms of NAP under the influence of DOM and iron minerals were explored in a riverside source area. Field dynamic monitoring data revealed that the NAP concentration in groundwater is mainly influenced by DOM, effective bound‑iron, and the intensity of river water infiltration recharge. Column experiments indicated that DOM with α-Fe2O3 or α-FeO(OH) reduced medium permeability by 8.16 % or 6.85 %, respectively, increasing water retention time. However, they had different effects on the attenuation of NAP. The coexistence of α-Fe2O3 and DOM enhanced NAP attenuation capacity by 9.13 %–45.91 %, while α-FeO(OH) and DOM reduced it by −13.25 % to −24.13 %. These effects were attributed to changes in the medium permeability, particle size, secondary mineral formation, and microbial community structure. Specifically, α-Fe2O3 and DOM reduced medium permeability, increasing the adsorption and biodegradation reaction time of NAP, and promoted secondary mineral (FeCO3) formation, increasing the adsorption capacity of medium for NAP, while α-FeO(OH) and DOM underwent cementation, resulting in larger particles and reduced adsorption capacity for NAP. Additionally, α-FeO(OH) and DOM promoted Shewanlla growth, inhibiting NAP attenuation by competing with NAP-degrading bacteria. These findings improve the understanding of the natural attenuation of polycyclic aromatic hydrocarbons (PAHs) in riverbank filtration, offering a basis for evaluating and controlling PAH pollution risks.

Characterization, source profiles and risk assessment of polycyclic aromatic hydrocarbons (PAHs) in urban dust of 14 Chinese cities

ABSTRACT Data for 16 USEPA priority PAHs were collected in urban dust from 14 cities in China between 2008 and 2022, and concentration, profile composition, and human health risk were investigated. The mean concentration of PAHs was 6.60 mg kg−1, ranging from 2.88 mg kg−1 to 13.88 mg kg−1, and it was higher than other important cities in neighboring countries of China. Among different individual PAHs, mean fluoranthene (Flr) was dominant, accounting for 15.04%, and low molecular weight PAH (LMW) was almost a third of high molecular weight PAH (HMW). The results of PAH composition profiles suggested that the proportion of different rings of PAHs increased in order: 2-ring PAHs (4.40%)< 6-ring PAHs (15.73%)< 3-ring PAHs (17.77%)< 5-ring PAHs (22.54%)< 4-ring PAHs (39.56%). The results of the source appointment suggested that pyrogenic sources and mixed sources, particularly wood, grass, coal, and diesel combustion, were the main sources of PAHs in urban dust. The results of the health risk assessment illustrated that children were more vulnerable to PAHs, and ingestion was the dominant exposure pathway to PAHs (78.152%, 67.519%, 73.206%, and 72.957% of children, adolescents, adults, and the total lifetime cancer risk (TLCR)). PAH pollution in urban dust from different cities in China was a commonly existing phenomenon, but the mean and maximum of TLCR were acceptable according to the standard established by USEPA (10−4). Based on Monte Carlo simulations, body weight (BW) was the most important uncertain input in three age groups (60.75%-91.22% contribution).

Competitive adsorption of polycyclic aromatic hydrocarbons on phosphorus tailing-modified sludge biochar provides mechanistic insights.

Biochar has been widely used to solve the wastewater pollution of polycyclic aromatic hydrocarbons (PAHs). However, the competition of PAHs with different benzene ring numbers (e.g., phenanthrene [Phe], pyrene [Pyr], and benzo[a]pyrene [BaP]) for adsorption sites on biochar has received little attention. In this study, biochar was produced by co-pyrolysis of sludge and phosphorus tailing at different temperatures (300, 500, or 800°C) to adsorb PAHs. The results show that phosphorus tailing increased the adsorption of PAH by increasing the biochar's BET surface area (SBET), micropore volume, hydrophobicity (at low temperatures) and aromaticity (at high temperatures). The maximum adsorption capacities were 29.90µmol/g for Phe, 25.58µmol/g for Pyr and 20.45µmol/g for BaP, respectively. Importantly, the types and functions of groups involved in the adsorption of various PAHs were discussed. Adsorption of Phe and Pyr on the biochar mainly involved C=O and C-O-C functional groups, and there was a certain degree of competition between these PAHs for those sites. In contrast, BaP mainly adsorbed at C-OH and C=C moieties, without competing with Phe or Pyr at C-OH sites. The competitive edge of BaP was also stronger than that of Phe and Pyr on C=C functional groups. The adsorption mechanisms involving pore filling, hydrophobic interactions, and π-π interactions governed the adsorption of the evaluated PAHs. Overall, the adsorption of PAHs on biochar followed a heterogeneous chemical adsorption process.

Overload of dissolved organic matter (DOM) in riparian infiltration zone increasing the pollution risk of naphthalene, insight from the competitive inhibition of naphthalene biodegradation by DOM.

Riparian infiltration zones are crucial for maintaining water quality by reducing the aqueous concentrations of polycyclic aromatic hydrocarbons (PAHs) through adsorption and biodegradation within the aquatic ecosystem. Dissolved organic matter (DOM) are ubiquitous in riparian infiltration zones where they extensively engage in the adsorption and biodegradation of PAHs, thereby influencing PAHs natural attenuation potential within riparian infiltration zones. Few studies have explored the natural attenuation mechanisms of PAHs influenced by DOM in riparian infiltration zones. In this study, the natural attenuation mechanisms of naphthalene (a typical PAHs component), under the influence of DOM, were explored, based on a case riverside source area. Analysis of microbial community structures, and the electron acceptor (e.g., Fe(III), DO/NO3-, SO42-)/electron donor (naphthalene and DOM) concentration changes within the riparian infiltration zone revealed a competitive inhibition relationship between DOM and naphthalene during microbial metabolism. Biodegradation experiments showed that when the concentration of DOM is higher than 4.0 mg·L-1, it inhibits the biodegradation of naphthalene. DOM competitively inhibits the biodegradation of naphthalene through the following mechanisms: (i) triggering microbial antioxidative defense mechanisms, diminishing the available resources for microbial participation in naphthalene degradation; (ii) altering microbial community structure; (iii) modulating microbial EPS composition, reducing the efficiency of microorganisms in utilizing carbon sources; and (iv) inhibiting the expression levels of downstream genes involved in naphthalene degradation. The competitive inhibition constants of DOM with concentrations of 1.0, 2.0, 4.0, 8.0, and 16.0 mg·L-1 on naphthalene biodegradation are -2.0 × 10-3, -5.0 × 10-3,1.0 × 10-3, 4.0 × 10-4, and 1.0 × 10-4, respectively. These findings enhance understanding of PAHs attenuation in riparian infiltration zone, providing a basis for assessing and managing PAHs pollution risks during riparian extraction.

SOURCE APPORTIONMENT OF ATMOSPHERIC AND SEDIMENTARY PAHS FROM KOLKATA, INDIA USING COMPOUND-CLASS-SPECIFIC RADIOCARBON ANALYSIS (CCSRA)

ABSTRACT Polycyclic aromatic hydrocarbons (PAHs) are major air pollutants that are ubiquitously produced by the combustion of organic materials, and it is extremely important to identify their pollution sources. In this study, molecular fingerprinting and compound class-specific radiocarbon dating (CCSRA) were performed on PAHs from canal sediments and air samples collected in Kolkata, India’s third largest city (population approximately 16 million), where PAHs pollution has been a serious problem. Average PAH (Σ12-parent PAHs) concentrations in air samples were 65.1 ng m–3 in summer and 70.9 ng m–3 in winter and in canal sediments were 32.7 µg g–1, which are classified as “very high-level” pollution. Molecular fingerprinting using methyl-PAH/PAH (MPAHs/PAHs) ratios and isomer pair ratios with molecular weights of 178, 202, 228, and 276 suggested that wood and coal combustion were the dominant sources of PAHs in the sediment, and that atmospheric PAHs were influenced by oil combustion in addition to them. The fraction of contemporary carbon (ƒC) of sedimentary PAHs (0.056–0.100), together with the extremely low MPAHs/PAHs ratio results, lead to the conclusion that the major source of the high concentration of PAHs in the canals is from coal combustion. On the other hand, the ƒC of atmospheric PAHs (0.272–0.369) was close to the share of biomass fuels in India’s domestic fuel consumption in 2011 (about 35%). Furthermore, the observed ƒC-discrepancy between atmospheric and sedimentary PAHs in the same urban environment was interpreted to give an insight into the loading pathway of PAHs to canal sediments in Kolkata.

Biodiversity of multi-trophic biological communities within riverine sediments impacted by PAHs contamination and land use changes

River ecosystems currently face a significant threat of degradation and loss of biodiversity resulting from continuous emissions of persistent organic pollutants and human activities. In this study, multi-trophic communities were assessed using DNA metabarcoding in a relatively stable riverine sediment compartment to investigate the biodiversity dynamics in the Beiluo River, followed by an evaluation of their response to polycyclic aromatic hydrocarbons (PAHs) and land use changes. A total of 48 bacterial phyla, 4 fungal phyla, 4 protist phyla, 9 algal phyla, 31 metazoan phyla, and 12 orders of fish were identified. The total concentration of PAHs in the Beiluo River sediments ranged from 25.95 to 1141.35 ng/g, with low molecular weight PAHs constituting the highest proportion (68.67%), followed by medium (22.19%) and high (9.14%) molecular weight PAHs. Notably, in contrast to lower trophic level aquatic communities such as bacteria, algae, and metazoans, PAHs exhibited a significant inhibitory effect on fish. Furthermore, the diversity of aquatic communities displayed obvious heterogeneity across distinct land use groups. A high proportion of cultivated land reduced the biodiversity of fish communities but increased that of metazoans. Conversely, an elevated proportion of built-up land reduced metazoan biodiversity, while simultaneously enhancing that of fungi and bacteria. Generally, land use changes exert both indirect and direct effects on aquatic communities. The direct effects primarily influence the abundance of aquatic communities rather than their diversity. Nevertheless, PAHs pollution may have limited potential to disrupt community structures through complex species interactions, as the hub species identified in the co-occurrence network did not align with those significantly affected by PAHs. This study indicates the potential of PAHs and land use changes to cause biodiversity losses. However, it also highlights the possibility of mitigating these negative effects in riverine sediments through optimal land use management and the promotion of enhanced species interactions.

Assessment of the contamination by carbonaceous anthropogenic particulates and polycyclic aromatic hydrocarbons (PAHs) concentration in recreational areas of an estuary heavily industrialized in Northern Spain

The commercial management of coal and its by-products has the potential to negatively impact natural coastal environments. The coal conversion processes and coke production are sources of polycyclic aromatic hydrocarbons (PAHs) emissions that also contribute to the pollution of those aquatic environments. This research assesses the contamination by carbonaceous anthropogenic particles and by polycyclic aromatic hydrocarbons of some recreational sites (Arañón, Peña del Caballo and San Balandrán area) located in the Avilés' estuary, an area in Northern Spain that has been heavily industrialized since the 1950s. The results obtained indicate a low concentration of solid organic anthropogenic particles in the intertidal sediments of the recreational sites in the estuary, probably due to the protective measures set in place at the facilities managing bulk coal and coke, which prevents the dispersion of coal dust (and other materials) as well as the eventual failure into the estuary. The characteristics of 16 priority pollutants PAHs analyzed in two recreational sites of the estuary (San Balandrán area), their distribution by aromatic ring number together with their diagnostic ratios demonstrate a pyrogenic nature with a main source from processes of coal and coke conversion (including combustion) in the facilities around the estuary. Some contribution of PAHs derived from petroleum cannot be ruled out. This contamination by PAHS is constant and sustained over time. The majority of the considered PAHs are well above the Spanish Generic Reference Level, (GRL) established for “protection of ecosystems with aquatic organisms”, and only a few of them are notably above the corresponding Spanish GRL established for “other uses of land”, which should include lands for recreational activities. The analysis of the potential toxicity risk of PAHs for human health and the organisms of the aquatic ecosystem suggests a relatively low toxicity risk to very high toxicity risk in the San Balandrán environment according to the concentration and distribution trend of PAHs identified in this area. This trend is dependent on the coastal dynamics and the protection level of the site, which also affect the distribution of the anthropogenic carbonaceous particulates in the same way.

Effects of stress metabolism on physiological and biochemical reaction and polycyclic aromatic hydrocarbons degradation ability of Bacillus. sp

A strain of Bacillus licheniformis T5 was isolated from soil contaminated with crude oil due to its efficient degradation of polycyclic aromatic hydrocarbons (PAHs). When subjected to stress metabolism using phenanthrene as a carbon source, significant changes were observed in T5 cells. Infrared spectrum analysis revealed the presence of -C=C- and Ph-O-C (aromatic) groups on the bacterial surface, facilitating the adsorption of PAHs on the phospholipid layer and causing damage to the cell membrane. Scanning electron microscope (SEM) analysis showed the changes of cell morphology, including a large number of folds on the lower surface and the folding of cell membrane. Transmission electron microscope (TEM) observation showed that non-stressed bacteria with adequate nutritional conditions accumulated more lipids. However, the stress group contained more protein. It was found that stress metabolism led to the increase of protein content in T5 cells by 16.4% and the activity of oxidoreductase more than doubled. These physiological and biochemical changes enhance the ability of stressed bacteria to degrade PAHs efficiently, thereby reducing the degradation cycle. The findings offer valuable insights for the remediation of PAHs pollution.

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.

Polycyclic aromatic hydrocarbons in fish from four lakes in central and eastern China: Bioaccumulation, pollution characteristics, sources, and health risk assessment

Polycyclic aromatic hydrocarbons (PAHs) are highly concerning environmental pollutants due to their toxicity, persistence, and bioaccumulation. In this paper, concentrations and compositions of 16 United States Environmental Protection Agency (USEPA) priority control PAHs in the fish collected from four lakes in central and eastern China were analyzed. 18 species of fish were collected from four typical lakes, namely Taihu Lake, Danjiangkou Reservoir, Yuncheng Salt Lake, and Nansi Lake. Quantitative analysis of PAHs were carried out with gas chromatograph/mass spectrometer, and 13 out of 16 PAHs were identified, with the main components being pyrene, chrysene, naphthalene, and benzo(b)fluoranthene. The accumulation of PAHs in fish from Taihu Lake, Danjiangkou Reservoir, Yuncheng Salt Lake, and Nansi Lake was 28.75–47.27, 26.60–31.93, 33.56–39.30, and 27.22–43.01 ng·g−1, respectively. The toxic equivalents of high-cyclic PAHs in fish of the four lakes were significantly higher than those of low-cyclic and middle-cyclic PAHs (P < 0.05). In Taihu Lake, Danjiangkou Reservoir, and Nansi Lake, the toxicity equivalents were predominantly contributed by benzo[a] pyrene (BaP), while in Yuncheng Salt Lake, dibenzo(a,h) anthracene (DahA) was the main contributor. The residents in central and eastern China exposed to PAHs had a negligible non-cancer risk (non-carcinogenic risk values <1) and a potential low cancer risk. It was noteworthy that the Pleuronichthys cornutus and Lateolabrax japonicus from Yuncheng Salt Lake could pose carcinogenic risks (>10−4) to humans, with benzo[b]fluoranthene (BbF) having the highest risk contribution rate. Source analysis indicated that the main source of PAHs in fish was combustion sources. BaP, DahA, and BbF could become potential pollutants of concern in the field of ecotoxicology. The results of this study on PAHs bioaccumulation, pollution characteristics, sources and health risks in fish from four lakes would provide a scientific basis for local governments to formulate targeted environmental management policies, pollution control measures, and public health strategies.

Exploring the characteristics and source-attributed health risks associated with polycyclic aromatic hydrocarbons and metal elements in atmospheric PM2.5 during warm and cold periods in the northern metropolitan area of Taiwan

Polycyclic aromatic hydrocarbons (PAHs) and metal elements are commonly considered hazardous air pollutants due to their toxic, mutagenic, and carcinogenic properties. However, few studies have simultaneously examined their potential sources and health effects. This study aimed to quantify the PAHs and metal elements in atmospheric PM2.5, investigating their characteristics and potential sources to assess associated health risks in the northern metropolitan area of Taiwan. The measurements indicated that the mean concentrations of total PAHs and metal elements in PM2.5 were 0.97 ± 0.52 ng m−3 and 590 ± 200 ng m−3, respectively. Utilizing the positive matrix factorization profiles, the PAH pollution was classified into two sources: industrial emissions, traffic emissions, and coal combustion (69%) were the predominant sources of PAHs, with petroleum volatilization and biomass burning (31%) making a lesser contribution. Similarly, we traced metal elements to three potential sources: natural sources (48%), a combined source of industrial emissions, coal combustion, and traffic exhaust (32%), and a blend of non-exhaust emissions from traffic and waste incineration sources (20%). Results from the potential source contribution function model suggested that the emissions of PAHs and metals could be influenced by the eastern regions of China, although local sources, including waste incinerators, traffic, shipping, and harbor activities, were identified as the primary contributors. Source-attributed excess cancer risk revealed that industry, traffic, and coal combustion had the highest cancer risk posed by PAHs in the cold period (1.0 × 10−5), while the greatest cancer risk among metal elements was linked to non-exhaust emissions from traffic and waste incineration emissions (2.0 × 10−5). This research underscores the importance of considering source contributions to health risk and emission reduction when addressing PM2.5 pollution. These findings have direct implications for policymakers, providing them with valuable insights to develop strategies that protect public health from the detrimental effects of PAH and metal element exposure.

Characterising polycyclic aromatic hydrocarbons in road dusts and stormwater in urban environments.

The presence of polycyclic aromatic hydrocarbons (PAHs) pollution on urban road surfaces is one of the major environmental concerns. However, knowledge on the distribution variability of PAHs in road dusts (RDS) and stormwater is limited, which would restrict the further risk evaluation and mitigation implementation of PAHs in road stormwater runoff. This study collected RDS samples and stormwater samples on fourteen urban roads in Shenzhen, China. This study investigated the variation of sixteen PAHs species in RDS and stormwater, and further evaluated the intrinsic and extrinsic factors which influence PAHs accumulation on urban road surfaces. The research outcomes showed significant differences on spatial distribution of PAHs in RDS and in stormwater. The land use types, industrial, commercial and port areas and vehicular volume have a positive relationship with PAHs abundance while dust particle size showed a negative correlation with PAHs abundance. For two phases in stormwater, fluctuation of PAHs with the rainfall duration in total dissolved solid (TDS) was more intensive than in dissolved liquid phase (DLP). This indicated when PAHs attached to RDS enter stormwater, most of PAHs still tend to be on solid particles than in liquid. The study outcomes are expected to contribute to efficient designs of PAHs polluted stormwater mitigation.

Enrichment characteristics of polycyclic aromatic hydrocarbons in coal gangue of the Huaibei Coalfield, China

Coal gangue, a by-product of coal mining, deteriorates and oxidizes, causing environmental pollution. Despite extensive research on polycyclic aromatic hydrocarbon (PAHs) pollution in soil, aerosols, and water, studies on PAHs in coal gangue remain limited. This study aimed to fill this research gap by analyzing gangue samples from three areas in Huaibei. Sixteen priority parent polycyclic aromatic hydrocarbons (16PAHs) and alkyl polycyclic aromatic hydrocarbons (aPAHs) in the samples were analyzed qualitatively and quantitatively via gas chromatography-triple quadrupole mass spectrometry. The results showed that PAHs existed naturally in coal gangue. The aPAHs concentration of multiple samples from the same area (587.88 ng/g, 2972.73 ng/g, and 13528.29 ng/g from Liuqiao, Suntan, and Tongting, respectively) was higher than the 16PAHs concentration (528.79 ng/g, 570.16 ng/g, and 2818.79 ng/g from Liuqiao, Suntan, and Tongting, respectively). Among the 39 samples, the aPAHs concentration after weathering was 7732.78 ng/g, which was higher than the value in the fresh state of 4765.43 ng/g. 16PAHs with low ring number were dominant in the fresh state, but aPAHs with high ring number were dominant after weathering. The diagnostic ratios revealed that traditional diagnostic ratios may confuse sources of PAHs and that gangue should be considered as a single class of source materials. Additionally, there was no significant difference in the ratio between the weathered and fresh state. TEQBaP analysis showed that there was a certain environmental risk in the area and that TEQBaP(weathered) > TEQBaP(fresh). Therefore, the pollution attributable to PAHs in coal gangue, especially weathered gangue, warrants attention.

Improved microbial-plant soil bioremediation of PAHs and heavy metal through in silico methods

The combined pollution of polycyclic aromatic hydrocarbons (PAHs) and organic cadmium (Cd) in farmland soils, and the field controlling strategy need to be studied urgently. In this study, 5 PAHs, 5 Cd and 11 soil conditioners were selected to explore the co-exposure risk and remediation efficiency. Firstly, a significant combination Fl-alkylalkoxy cadmium was obtained using forward and reverse methods coupling variation coefficient methods (the combined pollution value was 0.173). Secondly, the interaction energy of microbial degradation / plant absorption of Fl under Cd stress, and microbial mineralization / plant absorption of alkylalkoxy cadmium under PAHs stress were characterized using factorial experimental design, molecular docking and molecular dynamics simulation. The combined pollution of alkylalkoxy cadmium and dialkyl cadmium, phenanthrene and Benzo [a] pyrene was significant (synergistic contribution rates were 17.58 % and 19.22 %, respectively). In addition, 6 soil conditioners with significant efficiency were selected to design Taguchi orthogonal experimental schemes, indicating the microbial degradation / mineralization and plant absorption were significantly effective (the maximum increase of remediation efficiency was 93.81 %) under the combinations (i.e., trratone, coumarol, fulvamic acid, potassium fertilizer and others, etc.). Finally, it was found that the soil conditioners affected the hydrophobic groups and forces, and the efficiency was proportional to the highest peak value and minimum distance in the RDF curve. This study identifies the risk characteristics of co-exposure of PAHs and Cd and screens effective soil conditioners, providing theoretical guidance for risk controlling.

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.

Insight into interaction among soil microbial community, soil metabolomics and enzyme activity after long-term PAH stress

The problem of soil polycyclic aromatic hydrocarbon (PAH) pollution in coking plant sites has been widely studied in recent years, but there is a lack of research on the correlation between soil microorganisms, soil metabolomics, and soil properties. Thus, in this study, the long-term impact of coke combustion on soil microbial community structure, enzyme activities, and metabolic pathways within a former coking plant site was investigated. Soil samples were collected from both the coking production area (CA group) and office area (OLA group), approximately 0 to 20 cm in depth. Compared with OLA group, elevated levels of 16 PAHs in the list of USA EPA were detected by gas chromatography-mass spectrometry in the CA group. Several dominant microorganisms, such as Altererythrobacter, Lysobacter, and Sulfurifustis, were identified by 16 s ribosomal DNA sequencing in the CA group. The fatty acid biosynthesis pathway exhibited specific inhibition, while the phenylalanine metabolic pathway was promoted in response to PAH stress. Long-term PAH exposure led to the inhibition of soil urease activity. The co-occurrence network of microorganisms revealed intricate patterns of co-metabolism and co-adaptation within complex bacterial communities, facilitating their adaptation to and decomposition of soil-borne PAHs. This research could provide valuable insights into the community characteristics and metabolic mechanisms of microorganisms inhabiting PAH-polluted soil within coking plant sites. The findings enhance our understanding of the indigenous soil microbiome and its intricate network dynamics under the persistent stress of PAHs, contributing to a more comprehensive knowledge of soil ecosystems in such environments.

Biodegradation of high molecular weight polycyclic aromatic hydrocarbons by Sarocladium terricola strain PYR-233 isolated from petrochemical contaminated sediment

Polycyclic aromatic hydrocarbons (PAHs) were frequently found in sediment and were primarily treated through microbial degradation. Thus, efficient management of PAH pollution requires exploring the molecular degradation mechanisms of PAHs and expanding the pool of available microbial resources. A fungus (identified as Sarocladium terricola strain RCEF778) with the remarkable ability to degrade pyrene was screened from sediment near a petrochemical plant, and its growth and pyrene degradation characteristics were comprehensively investigated. The results showed that the fungus exhibited great effectiveness in pyrene degradation, with a degradation ratio of 88.97% at 21 days at the conditions: 35 °C, pH 7, 10 mg L−1 initially pyrene concentration, 3% supplementary salt, and glucose supplementation. The generation and concentration variation of the intermediate products were identified, and the results revealed that the fungus degraded pyrene through two pathways: by salicylic acid and by phthalic acid. Three sediments (M1, M2, M3), each exhibiting different levels of PAH pollution, were employed to examine the effectiveness of fungal degradation of PAHs in practical sediment samples. These data showed that with the fungus, the degradation ratios ranged from 13.64% to 23.50% for 2–3 rings PAHs, 40.93%–49.41% for 4 rings PAHs, and 39.59%–48.07% for 5–6 rings PAHs, which were significantly higher than those for the sediment without the fungus and confirmed the excellent performance of the fungal. Moreover, the Gompertz model was employed to analyze the degradation kinetics of 4-rings and 5–6 rings PAHs in these sediments, and the results demonstrated that the addition of the fungus could significantly increase the maximum degradation ratio, degradation start-up rate and maximum degradation rate of 4-rings and 5–6 rings PAHs and shorten the time required to reach the maximum degradation rate. This study not only supplied fungal materials but also established crucial theoretical foundations for the development of bioremediation technologies aimed at high molecular weight PAH-contaminated sediments.

Mechanistic study of OH radical-promoted decomposition of polycyclic aromatic hydrocarbon oxyradicals

Polycyclic aromatic hydrocarbons (PAHs) are widely recognized for their detrimental impact on human health and the atmospheric environment. One of the primary challenges in mitigating these effects is the efficient and rapid decomposition of PAH oxyradicals, a byproduct of PAH oxidation. This study aims to elucidate the promoting mechanism of hydroxyl (OH) radicals on the decomposition of PAH oxyradicals. Employing density functional theory and transition state theory, we systematically investigate the decomposition mechanism of PAH oxyradicals under the influence of OH radicals. Our findings indicate that the interaction between OH radicals and PAH oxyradicals constitutes a pivotal oxidation process within flames. Notably, PAH oxyradicals are more inclined to undergo pyrolysis subsequent to their reaction with OH radicals within a flame, as opposed to direct pyrolysis. This observation underscores the role of OH radicals in facilitating the decomposition of PAH oxyradicals in flame conditions. Further analysis reveals that OH radicals can effectively react with various forms of PAH oxyradicals—zigzag, free, and armchair—leading to the formation of OH-OPAH compounds characterized by HO-C-O functional groups. Importantly, this addition reaction between OH radicals and PAH oxyradicals is found to be independent of the edge types of the PAH oxyradicals. The pyrolysis of OH-OPAH predominantly yields products such as COOH, CO2, and PAHs with five-membered rings, with COOH emerging as the primary oxidation product. This pyrolysis predominantly proceeds via a ring-opening reaction, rather than through cyclization. This study also reveals that the likelihood of PAH oxyradical pyrolysis increases with the number of free edges surrounding the oxygen-containing functional groups. Furthermore, the oxidation activity of the HO-C-O functional group is demonstrated to be more potent than that of the C-O functional group, significantly enhancing the reactivity of PAH oxyradical degradation in the presence of OH radicals. These insights not only contribute to refining the combustion model of PAH oxidation but also advance our understanding of PAH oxyradical decomposition. Such knowledge is crucial for the development and optimization of control technologies targeting PAH pollutants emanating from combustion devices.

Ultrafine CuO/graphene oxide cellulose nanocomposites with complementary framework for polycyclic aromatic hydrocarbon pollutants removal

Efficient and sustainable methods for eliminating polycyclic aromatic hydrocarbon pollutants (PAHPs) are in highly desired. Proven technologies involve physical and chemical reactions that absorb PAHPs, however they encounter formidable challenges. Here, a bottom-up refining-grain strategy is proposed to rationally design ultrafine CuO/graphene oxide-cellulose nanocomposites (LCelCCu) with a mirror-like for tetracycline (TC) to substantially improve the efficient of the purification process by active integrated-sorption. The LCelCCu captures TC with a higher affinity and lower energy demand, as determined by sorption kinetic, isotherms, thermodynamics, and infrared and X-ray Photoelectron Spectroscopy. The resulting material could achieve ultra-high sorption capacity (2775.23 mg/g), kinetic (1.2499 L g−1 h−1) and high selectivity (up to 99.9 %) for TC, nearly surpassing all recent adsorbents. This study simultaneously unveils the pioneering role of simultaneous multi-site match sorption and subsequent advanced oxidation synergistically, fundamentally enhancing understanding of the structure-activity-selectivity relationship and inspires more sustainable water purification applications and broader material design considerations.

Polycyclic aromatic hydrocarbon (PAH) accumulation in selected medicinal plants: a mini review.

The use of plant-based products in healthcare systems has experienced a tremendous rise leading to a substantial increase in global demand. However, the quality and effectiveness of such plant-based treatments are often affected due to contamination of various pollutants including polycyclic aromatic hydrocarbons (PAHs). Like other plants, medicinal plants also uptake and accumulate PAHs when exposed to a contaminated environment. The consumption of such medicinal plants and/or plant-based products causes negative effects on health rather than providing any therapeutic advantages. Unfortunately, research focusing on PAH accumulation in medicinal plants has received very limited attention. This review discusses a sizable number of literature regarding the concentration of sixteen priority PAH pollutants as recognised by the US Environmental Protection Agency (USEPA) in different medicinal plants. The review also highlights the risk assessment of cancer associated with some medicinal plants in terms of benzo[a]pyrene (BaP) equivalent concentrations.