Ring Polycyclic Aromatic Hydrocarbons Research Articles

Emission profiles, source identifications, and health risk of polycyclic aromatic hydrocarbons (PAHs) in a road tunnel located in Xi'an, China.

Understanding the sources and characteristics of PM2.5-bound PAHs from traffic-related pollution can provide valuable data for mitigating air contamination from traffic in local urban regions. However, little information on PAHs is available regarding the typical arterial highway-Qinling Mountains No.1 tunnel in Xi'an. We estimated the profiles, sources, and emission factors of PM2.5-bound PAHs in this tunnel. The total PAH concentrations were 22.78 ng·m-3 and 52.80 ng·m-3 at the tunnel middle and exit, which were 1.09 and 3.84 times higher than that at the tunnel entrance. Pyr, Flt, Phe, Chr, BaP, and BbF were the dominant PAH species (representing approximately 78.01% of total PAHs). The four rings PAHs were dominant (58%) among the total PAH concentrations in PM2.5. The results demonstrated that diesel and gasoline vehicles exhaust emissions contributed 56.81% and 22.60% to the PAHs, respectively, while the corresponding value for together brakes, tyre wear, and road dust was 20.59%. The emission factors of total PAHs were 29.35 μg·veh-1·km-1, and emission factors of 4 rings PAHs were significantly higher than those of the other PAHs. The sum of ILCR was estimated to be 1.41×10-4, which accorded with acceptable level of cancer risk (10-6-10-4), PAHs should not ignored as they still affect the public health of inhabitants. This study shed light on PAH profiles and traffic-related sources in the tunnel, thereby facilitating the assessment of control measures targeting PAHs in local areas.

Characterization, sources, and risk assessment of PAHs in borehole water from the vicinity of an unlined dumpsite in Awka, Nigeria

Polycyclic aromatic hydrocarbons (PAHs) are contaminants of interest in the ecosystem due to associated health risks. Therefore, their detection in the environment is important. In this regard, the risk assessment of PAHs in borehole water near the unlined dumpsite in Anambra State was investigated. Samples of borehole water (16 each) were collected from the study and control areas during both seasons. The PAH concentrations in the borehole water samples were analyzed using gas chromatography. The mean PAH concentration in the study and control samples for the wet season varied from BL–7.65 µg/L to BL–2.98 µg/L, respectively. The study samples' dry season values ranged from BL to 3.33 µg/L, while control samples ranged from BL to 1.87 µg/L. sumPAHs for the wet and dry seasons varied from 5.8 to 13.94 µg/L and 4.25 to 10.09 µg/L for study and control samples, respectively. The four and five rings PAH were the most dominant group in the sum PAHs for the study and control samples, respectively. Diagnostic ratios suggested pyrolytic and petrogenic sources for both locations. The cluster analysis showed different sources of the congeners in the samples. The non-carcinogenic risk showed no possibility of risks via dermal and ingestion routes. In addition, the possibility of cancer risks via ingestion routes was doubtful. The carcinogenic risk index through dermal contact exceeded the acceptable limit for adults and is at a tolerable limit for children, indicating potential threats to humans, with adults more susceptible to cancer risks. Therefore, this study recommends that sanitary dumpsites be constructed for waste disposal and implementation of environmental laws to prevent underground water pollution and the environment.

Evolutions of functional groups and polycyclic aromatic hydrocarbons during low temperature pyrolysis of a perhydrous bituminous coal

Understanding the molecular structural evolution mechanism during coal pyrolysis can help better regulate coal conversions for developing clean coal technology. This study investigated changes in functional groups and polycyclic aromatic hydrocarbons (PAHs) during pyrolysis of a perhydrous bituminous coal at temperature of 75–600 °C. Results indicated that aliphatic, C–O, C=O, OH, aromatic C=C, and aromatic C–H groups declined in relative abundance below 300 °C. These declines were attributed to cracking of hydrogen bonds and devolatilization. Meanwhile, the alkyl side chains of alkylated PAHs, i.e., alkyl-naphthalenes and alkyl-phenanthrenes, were continuously detached. Pyrolysis at 300–450 °C was characterized by elevated aromaticity, reflected by increments in the relative abundances of aromatic C–H, aromatic carbon, pyridine nitrogen, and protonated carbon. PAH evolutions at this stage exhibited relative increases of 4-–6-ring PAHs with relative decreases of 2-–3-ring PAHs. Pyrolysis at 450–600 °C was characterized by an increment of aromatic C=C and significant increases in relative abundances of 4-–6-ring PAHs in emitted particulate and gaseous phases. The elevation of pyrolysis temperature transformed coal macromolecules into more compact structure. The molecular structural units of chars were formulated as C245H227N3O14S, C239H193N3O8S, C228H152N2O3S, and C221H113NO3S for coal and chars produced at 300, 500, and 600 °C, respectively. Changes in three-dimensional molecular structural units reflected step-by-step intense deformation and condensed process.

Effects of pyrolysis conditions and heteroatom modification on the polycyclic aromatic hydrocarbons profile of biochar prepared from sorghum distillery residues

The formation of 2- to 6-ring polycyclic aromatic hydrocarbons (PAHs) in sorghum distillery residue-derived biochar (SDRBC) was evaluated under different thermochemical pyrolysis conditions of carbonization atmosphere (N2 or CO2), temperature (300–900 °C) and doping with nonmetallic elements, i.e., N, B, O, P, N + B, and N + S. The results indicated that without surface modification, PAHs formation was 944 ± 74 ng g–1, the highest level, and 181 ± 16 ng g–1, the lowest level, at 300 °C in N2 and CO2 atmosphere, respectively. Boron doping of SDRBC significantly reduced the PAHs content (by 97%) under N2 at 300 °C. Results demonstrated that boron modified SDRBC exhibited the highest degree of PAHs reduction. Combined pyrolysis temperature and atmosphere in addition to heteroatom doping is a robust and viable strategy for efficient suppression of PAHs formation and high-value utilization of pyrolysis products of low carbon footprint.

Insights into the effects of hydrogen peroxide and Fenton oxidation on PAHs removal and indigenous microorganisms in a coking-contaminated soil

Polycyclic aromatic hydrocarbons (PAHs) are typical persistent organic pollutants in the coking-contaminated soil, however, the effects of chemical oxidation on PAHs removal and the responses of indigenous microorganisms in slurry system has not been studied. In this study, the removal efficiency of PAHs and the responses of indigenous microorganisms treated by hydrogen peroxide (H2O2) and Fenton oxidation under different liquid-to-solid (L/S) ratio were investigated. The results showed that the highest removal efficiency of Σ PAHs treated by H2O2 oxidation was at the L/S ratio of 4:1. At such condition, the order of PAHs removal efficiency from high to low was 3-ring PAHs (69.7%–99.9%), followed by high ring PAHs (4-6 rings, 54.5%–95.5%), and 2-ring PAHs (38.1%–52.4%). However, Fenton oxidation had insignificantly increased the removal efficiency of PAHs, partly because the high content of metal cations (i.e., Fe2＋ and Mn2+) in coking contaminated soil. The number of soil microorganisms changed slightly during H2O2 and Fenton oxidation treatments (∼10 8 copies/g), while the bacterial diversity increased significantly. Microbial function analysis suggested that the carbohydrate metabolism, xenobiotics biodegradation and metabolism mainly contributed to the degradation of PAHs. Moreover, the function genes and pathways (i.e., amino sugar metabolism and citrate cycle) that involved in PAHs biodegradation increased, which can further promote the biological degradation of PAHs by indigenous microorganisms.

Concentrations, phase exchanges and source apportionment of polycyclic aromatic hydrocarbons (PAHs) In Bursa-Turkey

The present study aimed to determine the pollution levels derived from polycyclic aromatic hydrocarbons (PAHs) in air, plant and soil samples and to reveal the PAH exchange at the soil-air, soil-plant and plant-air interfaces. In this context, air and soil samples were collected in approximately 10-day periods between June 2021 and February 2022 from a semi-urban area in Bursa, an industrial city with a dense population. Also, plant branch samples were collected for the last three months. Total PAH concentrations in the atmosphere (∑16PAH) and soil (∑14PAH) ranged from 4.03 to 64.6 ng/m3 and 13–189.4 ng/g DM, respectively. PAH levels in the tree branches varied between 256.6 and 419.75 ng/g DM. In all air and soil samples, PAH levels were low in the summer and reached higher values in the winter. 3-ring PAHs were the dominant compounds, and their distribution in air and soil samples varied between 28.9%-71.9% and 22.8%–57.7%, respectively. According to the results of diagnostic ratios (DRs) and principal component analysis (PCA), both pyrolytic and petrogenic sources were found to be effective in PAH pollution in the sampling region. The fugacity fraction (ff) ratio and net flux (Fnet) values indicated that the direction of movement of PAHs was from soil to air. In order to better understand the PAH movement in the environment, soil-plant exchange calculations were also achieved. The ratio of ∑14PAH values measured to modeled concentrations (1.19<ratio<1.52) revealed that the model worked well for the sampling region and produced reasonable results. The ff and Fnet levels showed that branches were saturated with PAHs and the direction of PAH movement was from plant to soil. The plant-air exchange results indicated that the direction of movement of PAHs was from plant to air for low molecular weight PAHs and the opposite was true for compounds with high molecular weight ones.

Relationship between atmospheric pollution and polycyclic aromatic hydrocarbons in fresh snow during heavy pollution episodes in a cold city, northeast China

Air quality index (AQI) and air pollutants during two typical pollution episodes, and polycyclic aromatic hydrocarbons (PAHs) in fresh snow after each episode in the winter 2019 across Harbin City in northeast China were investigated to explore the co-environmental behaviors. Significantly greater values of AQI and PAHs were found in the more serious atmospheric pollution episode (episode Ⅱ), demonstrating that PAHs in fresh snow is a robust indicator. PM2.5 was the primary air pollutant in both episodes based on PM2.5/PM10 ratios, which might be attributed to fine particulate converted from gas-to-particle process. PM2.5 and 4-ring PAHs significantly positive correlated, indicating that airborne particulate PAHs were co-emitted and co-transported with atmospheric fine particles released from coal combustion and vehicular emission under low temperature and high relative humidity. 3- and 4- rings PAHs were dominant in episode Ⅱ, while 5- and 6- rings PAHs were found the lowest in both episodes. These characteristics reflected that long-range transportation of coal and biomass burning were from the surrounding areas, while vehicle exhausts were mainly from local emissions. Except for the impact of local pollution source emissions, the regional transport could make a greater contribution in a more serious pollution event.

Bioaccumulation characteristics of typical pollutants in seafood from coastal waters of Jiangsu, China

With the increasing human activities, marine ecosystems and biodiversity are under serious threat, in particular, pollutants in the environment can be enriched in organisms and transmitted along the food chain, potentially posing a health risk to humans. Accordingly, with the common economic swimming animals in the coastal waters of Jiangsu as the research samples, this study analyzed the content and distribution characteristics of typical pollutants (heavy metals and polycyclic aromatic hydrocarbons (PAHs)) enriched in their bodies, and assessed their dietary exposure and health risks to humans. We showed that the bioaccumulation capacity of swimming animals for Zn and Cu was high, with the lowest accumulated content of Hg, and that crustaceans were more easily enriched with heavy metals than fish. The overall evaluation results showed that the heavy metal content in Jiangsu coastal swimming animals was relatively safe, but the health risk of some swimming animals was high and warranted certain attention. Additionally, PAHs was more enriched in inshore swimming animals than in marine ranch area and was consistent with the enrichment characteristics of swimming animals for heavy metals, with crustaceans being more enriched in PAHs. PAHs in swimming animals had the highest proportion of 2–3 ring PAHs, accounting for 75.82%, and their incremental lifetime carcinogenic risks (ILCR) in swimming animals were all within the acceptable risk values. These findings shed light on the effects of typical pollutants on swimming animals in the coastal waters of Jiangsu, provide a scientific basis for accurately assessing the effects of marine environmental pollution on marine fishery resources and food quality and safety, and contribute to new data support for regional fisheries management and environmental pollution monitoring.

The association of in-utero exposure to polycyclic aromatic hydrocarbons and umbilical liver enzymes

BackgroundThe adverse health influences of polycyclic aromatic hydrocarbons (PAHs) exposures have been examined in several previous research. However, the evidence on the health influences of PAHs exposure during pregnancy and childhood is scarce, with no study on the infant's liver function. Therefore, in this study, the association of in-utero exposure to particulate matter-bound PAHs (PM-bound PAHs) on the umbilical liver enzymes was investigated. MethodsA total of 450 mother-pair samples were assessed in this cross-sectional study in Sabzevar, Iran (2019–2021). The concentrations of PM-bound PAHs were estimated based on spatiotemporal models at residential addresses. The umbilical cord blood alkaline phosphatase (ALP), aspartate aminotransferase (AST), alanine aminotransferase (ALT), and gamma-glutamyl transferase (GGT) were measured as indicators of infant's liver function. The association of PM-bound PAHs with umbilical liver enzymes was evaluated using multiple linear regression, controlled for relevant covariates. The quantile g-computation (g-comp) was used to investigate the combined impact of the 15 PAHs on liver function biomarkers. ResultsHigher levels of total 4-ring PAHs, Dibenzo[a,h]anthrancene, Anthracene, Pyrene, Benzo[a]anthracene, Phenanthrene, Fluorene, Acenaphthylene and Naphthalene were associated with higher umbilical ALP. An increase in total 5-ring PAHs, Benzo[g,h,i]perylene, Benzo[a]pyrene and Chrysene was associated with higher umbilical AST levels. Each 1 ng/m3 increase in exposure to Benzo[g,h,i]perylene was related with 182.21 U/L (95 % CI: 116.11, 248.31, P < 0.01) increase in umbilical GGT. PAHs mixture exposure was positively associated with higher umbilical AST and ALT, while no significant associations were noted for ALP and GGT. We observed a potentially stronger association for girls compared to boys based on umbilical ALT and AST. However, for GGT and ALP, these associations were stronger for boys compared to girls. ConclusionOverall our findings suggested that exposure to PAHs during pregnancy had adverse effects on infant's liver function.

Effects of organic carbon/elemental carbon and particle size on inhalation bioaccessibility of particle-bound PAHs

Bioaccessible fractions of particle-bound hydrophobic organic compounds (HOCs) are critical to evaluating human inhalation exposure risk. However, the key factors for controlling the release of HOCs into the lung fluid are not adequately examined. To address this issue, eight particle size fractions (0.056–18 μm) from different particle emission sources (barbecue and smoking) were collected and incubated with an in vitro method for determining inhalation bioaccessibilities of polycyclic aromatic hydrocarbons (PAHs). The bioaccessible fractions of particle-bound PAHs were 35–65% for smoke-type charcoal, 24–62% for smokeless-type charcoal, and 44–96% for cigarette. The size distributions of bioaccessible fractions of 3–4 ring PAHs were symmetric with the patterns of their masses, characterized as a unimodal distribution with both the trough and peak at 0.56–1.0 μm. Analysis from machine learning showed that chemical hydrophobicity appeared to be the most significant factor affecting inhalation bioaccessibility of PAHs, followed by organic carbon and elemental carbon contents. Particle size seemed to have little effect on the bioaccessibility of PAHs. A compositional analysis of human inhalation exposure risk from total concentration, deposition concentration, and bioaccessible deposition concentration in alveolar region showed a shift in the key particle size from 0.56−1.0 μm to 1.0–1.8 μm and an increasing in the contributions of 2–3 ring PAHs to risk for cigarette due to the high bioaccessible fractions. These results suggested the significance of particle deposition efficiency and bioaccessible fractions of HOCs in risk assessment.

Effectively removing gaseous polycyclic aromatic hydrocarbons (PAHs) by willow catkins: Do you still dislike the catkins floating?

The floating catkins generated by willow and poplar trees have been criticized for spreading germ and causing fire for decades. It has been found that catkins are with a hollow tubular structure, which made us wonder if the floating catkins can adsorb atmospheric pollutions. Thus, we conducted a project in Harbin, China to investigate whether and how willow catkins could adsorb atmospheric polycyclic aromatic hydrocarbons (PAHs). The results suggest that both the catkins floating in the air and on the ground preferred to adsorb gaseous PAHs rather than particulate PAHs. Moreover, 3- and 4-ring PAHs were the dominating compositions adsorbed by catkins, which significantly increased with exposure time. The gas/catkins partition (KCG) was defined, which explained why 3-ring PAHs are more easily adsorbed by catkins than by airborne particles when their subcooled liquid vapor pressure is high (log PL > −1.73). The removal loading of atmospheric PAHs by catkins were estimated as 1.03 kg/year in the center city of Harbin, which may well explain the phenomenon that levels of gaseous and total (particle + gas) PAHs are relatively low in the months with catkins floating reported in peer-reviewed papers.

Distribution, source, and risk assessment of polycyclic aromatic hydrocarbons (PAHs) in surface sediments from Dingzi Bay, China

This study dissected 21 surface sediment samples collected from the vicinity of Dingzi Bay to understand the distribution and ecological risk of PAHs. The findings revealed that the concentration of PAHs in sediments ranged from 71.38 ng·g−1 to 163.28 ng·g−1, with an average of 106.43 ng·g−1. The main components were 3-ring PAHs. By using the diagnostic ratio and principal component analysis (PCA) approach, it was determined that the main sources of PAHs in the sediments in this region were biomass, coal combustion, and oil leaks. The majority of PAHs have low ecological risk, with just Acenaphthene having slightly higher concentrations than ERL, according to the effective range low and median approaches (ERL and ERM). The examination of the toxic equivalent approach revealed that PAHs in the research area had low levels of toxicity and ecological risk.

Evaluation of polycyclic aromatic hydrocarbons in sediments of Balsas River Mouth, Pacific Coast, Mexico: Sources, risks, and genotoxicity

Polycyclic aromatic hydrocarbons (PAHs) were assessed in sediments (n = 7) collected from the mouth of the Balsas River, Pacific Coast, Mexico. The total PAH levels ranged between 142.1 and 3944.07 μg kg−1 in the summer and 137.65–3967.38 μg kg−1 in the winter, probably reflecting the anthropogenic activities of the region. Calculation of the four analytical ratios of [Anthracene/(Anthracene + Phenanthrene)]: [Fluoranthene/(Fluoranthene + Pyrene)], [Fluoranthene/Pyrene: Fluoranthene/(Fluoranthene + Pyrene)], [Indeno [123-cd]Pyrene/(Indeno [123-cd]Pyrene + Benzo [ghi]Perylene)]: [Benzo [a]anthracene/(Benzo [a]Anthracene + Chrysene)], and [Anthracene/Phenanthrene]: [Fluoranthene/(Fluoranthene + Pyrene)] revealed a mixed PAH source, from petroleum and biomass combustion. Significant statistical correlations (r2 = 0.90) between the 4 and 5 ringed PAHs denote that adsorption is the principal mechanism for accumulation in sedimentary archives. Ecotoxicological indices (Mean Effect Range Medium Quotient and Mean Probable Effect Level Quotient) indicated moderate pollution with adverse biological impacts on ambient benthonic organisms. The calculations of Toxicity Equivalent Quotient and Mutagen Equivalent Quotient values proposed that the region is highly polluted by mutagenic and carcinogenic PAH compounds. The genotoxic evaluation of Lutjanus guttatus (Spotted rose snapper) presented significant DNA damage and discrepancies in Ethoxyresorufin-O-Deethylase activity. Based on the toxicological and genotoxicological evaluation of PAHs in sediments, the region was observed to be largely impacted from biological damage.

Controlling Diels-Alder reactions in catalytic pyrolysis of sawdust and polypropylene by coupling CO2 atmosphere and Fe-modified zeolite for enhanced light aromatics production

Producing value-added light aromatics (BTEX) from solid waste streams holds excellent promise for resource recovery. Here we present a thermochemical conversion approach that enhanced BTEX production by coupling CO2 atmosphere and Fe-modified HZSM-5 zeolite to facilitate the Diels-Alder reactions in catalytic pyrolysis of sawdust and polypropylene. The Diels-Alder reactions between sawdust-derived furans and polypropylene-derived olefins could be controlled by tuning CO2 concentration and Fe loading amount. Sufficient CO2 (≥50%) with moderate Fe loading (10 wt%) were observed to produce more BTEX and fewer heavy fractions (C9+aromatics). To deepen the mechanistic understanding, quantification of polycyclic aromatic hydrocarbons (PAHs) and catalyst coke was further conducted. The co-use of CO2 atmosphere and Fe modification suppressed the appearance of low-, medium-, and high-membered ring PAHs by over 40%, decreased pyrolysis oil toxicity from 42.1 to 12.8 μg/goil TEQ, and transformed coke from "hard" to "soft". Based on the characterization of CO2 adsorption behavior, it was deduced that the introduced CO2 was activated by loaded Fe and reacted in situ with H2 generated during aromatization to expedite H-transfer. Meanwhile, BTEX recondensation was prevented through the Boudouard reactions of CO2 and water-gas reactions between the resulting water and carbon deposits. These synergistically enhanced the production of BTEX and suppressed the formation of heavy species, including PAHs and catalyst coke.

Complexation of Selected Polycyclic Aromatic Hydrocarbons with Hexaprotonated Hexaazacyclophane Macrocycles

Abstract: This research focused on the host-guest complexation-driven detection of three selected polycyclic aromatic hydrocarbons (PAHs), naphthalene, anthracene and phenanthrene, in solution using two protonated hexaazacyclophane macrocycles (16+), specifically 1a6+ and 1b6+. The geometry optimization of PAHs and 16+ performed using quantum chemical density functional theory calculations demonstrated their electronic compatibility to undergo host-guest complexation. The macrocycles 1a6+ and 1b6+, which possess different cavity geometries, were synthesized using [2+2] Schiff-base cyclization of diethylenetriamine separately with terephthalaldehyde and isophthalaldehyde, respec-tively, followed by reduction and protonation. After spectroscopic characterization of the macrocycles, the fluorescence spectroscopic determination of stoichiometry, binding constant and quenching constant between 1a6+/1b6+ and PAH was performed using the Job’s plot method, Benesi-Hildebrand method and Stern-Volmer plot, respectively. The stoichiometry of each combination of 16+ with PAH exhibits a 1:1 complexation. Among the PAHs studied, phenanthrene demonstrated the highest binding and quenching constants with both 16+, while anthracene and naphthalene showed the lowest binding and quenching constants, respectively, with both 16+. The cavity geometry of 16+ and the shape and number of fused rings of PAHs contributed to the binding constant.

Health Risk Assessment of Polycyclic Aromatic Hydrocarbons from Cooking Fuels burning in Nigeria

Cooking activities are an important source of indoor air pollution which contributes significantly to Polycyclic Aromatic Hydrocarbons (PAHs) in the environment. This study investigated sixteen (16) priority PAHs emitted from smoke in eight (8) cooking fuels commonly used in Nigeria. Gas Chromatography Mass Spectrometry (GC-MS) was used for sample analysis and the potential health risk associated with exposure to PAHs were evaluated. The highest total quantified PAHs concentration was obtained from the burning of palm kernel fiber with an average ΣPAHs of 14.06 mg/kg. The result showed a variation in the average concentration of 10.82 − 14.06 mg/kg for all the cooking fuels. 3-ringed PAHs were found to be the dominant PAHs in the samples considered in terms of concentrations and frequency of occurrence at 7.03-9.42 mg/kg. Benzo[a]anthracene was the most abundant PAHs in biomass materials while Benzo[a]pyrene was the most abundant in liquified petroleum gas and Benzo[b]fluoranthene in kerosene. The cancer risk for both the children and adult obtained for all the cooking fuel samples were less than 10 − 6 which is satisfactory except in sawdust which has a value of 1.30 × 10 − 5 and 1.44 × 10 − 5 for child and adult, respectively. It is recommended that cleaner cooking fuels be used in well-ventilated environments to reduce exposure to these pollutants. Highlights Sixteen priority PAHs in emissions from the burning of eight cooking fuels in Nigeria were investigated Emission sources of the PAHs were identified using diagnostic ratios Health risks of PAHs in emissions from the burning of cooking fuels is higher in adult

Deep relationships between bacterial community and polycyclic aromatic hydrocarbons in soil profiles near typical coking plants.

Bacterial communities play an important role in maintaining the normal functioning of ecosystems; therefore, it is important to understand the effects of polycyclic aromatic hydrocarbons (PAHs) on the bacterial community. In addition, understanding the metabolic potential of bacterial communities for PAHs is important for the remediation of PAH-contaminated soils. However, the deep relationship between PAHs and bacterial community in coking plants is not clear. In this study, we determined the bacterial community and the concentration of PAHs in three soil profiles contaminated by coke plants in Xiaoyi Coking Park, Shanxi, China, using 16S rRNA and gas chromatography coupled with mass spectrometry, respectively. The results show that 2 ~ 3 rings PAHs are the main PAHs and Acidobacteria (23.76%) was the dominant bacterial community in three soil profiles. Statistical analysis showed that there were significant differences in the composition of bacterial communities at different depths and different sites. Redundancy analysis (RDA) and variance partitioning analysis (VPA) illustrate the influence of environmental factors (including PAHs, soil organic matter (SOM), and pH) on the vertical distribution of soil bacterial community, and PAHs were the main factors affecting the bacterial community in this study. The co-occurrence networks further indicated correlations between bacterial community and PAHs and found that Nap has the greatest effect on bacterial community compared with other PAHs. In addition, some operational taxonomic units (OTUs, OTU2, and OTU37) have the potential to degrade PAHs. PICRUSt2 (Phylogenetic Investigation of Communities by Reconstruction of Unobserved States) was used for further study on the potential of microbial PAHs degradation from a genetic perspective, which showed that different PAH metabolism genes were present in the genomes of bacterial communities in the three soil profiles, and a total of 12 PAH degradation-related genes were isolated, mainly dioxygenase and dehydrogenase genes.

Remediating petroleum hydrocarbons in highly saline–alkali soils using three native plant species

Phytoremediation of total petroleum hydrocarbons (TPHs) contamination is a process that uses the synergistic action of plants and rhizosphere microorganisms to degrade, absorb and stabilize pollutants in the soil, and has received increasing attention in recent years. However, this technology still has some challenges under certain conditions (e.g., highly alkaline and saline environments). The present study was selected three native plant species (alfalfa, tall fescue, and ryegrass) to remediate petroleum pollutants in greenhouse pot experiments. The results indicate that TPH contamination not only inhibited plant growth, soil chemical properties and soil fertility (i.e. lower plant biomass, chlorophyll, pH, and electrical conductivity), but also increased the malondialdehyde, glutathione, and antioxidant enzyme activities (catalase and polyphenol oxidase). Further, correlation analysis results illustrated that TPH removal was strongly positively correlated with chlorophyll, soil fertility, and total organic carbon, but was negatively correlated with dehydrogenase, polyphenol oxidase, pH, and electrical conductivity. The highest TPHs removal rate (74.13%) was exhibited by alfalfa, followed by tall fescue (61.79%) and ryegrass (57.28%). The degradation rates of short-chain alkanes and low rings polycyclic aromatic hydrocarbons (PAHs) were substantially higher than those of long-chain alkanes and high rings PAHs. The findings of this study provide valuable insights into petroleum decontamination strategies in the highly saline - alkali environments.

Occurrence Characteristics, Sources, and Toxicity Risk Analysis of Polycyclic Aromatic Hydrocarbons in Typical Rivers of Northern Shaanxi Mining Area, China

The aim of this study was to assess the occurrence level, spatial distribution, pollution source, and ecological risk of polycyclic aromatic hydrocarbons (PAHs) in the Kuye River of the northern Shaanxi mining area. In total, 16 priority PAHs were quantitatively detected at 59 sampling sites using a high-performance liquid chromatography-diode array detector in series with a fluorescence detector. The results showed that the ρ(ΣPAHs) in the Kuye River ranged from 50.06 to 278.16 ng·L-1, with an average value of 128.22 ng·L-1. The PAHs monomer concentrations ranged from 0 to 121.22 ng·L-1, of which Chrysene had the highest concentration, with average values of 36.58 ng·L-1, respectively, followed by benzo(a)anthracene and phenanthrene. The detection rate of each monomer was more than 70%, of which 12 monomers revealed detection rates of 100%. In addition, the 4-ring PAHs showed the highest relative abundance in the 59 samples, ranging from 38.59% to 70.85%. The PAHs concentrations revealed significant spatial variation in the Kuye River. Moreover, the highest PAHs concentrations were mainly observed in coal mining, industrial, and densely populated areas. Compared with those in other rivers in China and worldwide, the PAHs concentrations in the Kuye River showed a medium pollution level. On the other hand, the positive definite matrix factorization (PMF) and diagnostic ratios were used to quantitatively assess the source apportionment of PAHs in the Kuye River. The results showed that coking and petroleum emissions, coal combustion, fuel-wood combustion, and automobile exhaust emissions contributed to the PAHs concentrations in the industrial areas of the upper reach by 34.67%, 30.62%, 18.11%, and 16.60%, and coal combustion, fuel-wood combustion, and automobile exhaust emissions contributed in the downstream residential areas by 64.93%, 26.20%, and 8.86%. In addition, the results of the ecological risk assessment showed low ecological risks of naphthalene and high ecological risks of benzo(a)anthracene, respectively, whereas the remaining monomers revealed medium ecological risk. Among the 59 sampling sites, only 12 belonged to low ecological risk areas, whereas the remaining sampling sites were at medium to high ecological risks. Moreover, the water area near the Ningtiaota Industrial Park showed a risk value close to the high ecological risk threshold. Therefore, it is urgent to formulate prevention and control measures in the study region.

Bitumen fumes and PAHs in asphalt road paving: Emission characteristics, determinants of exposure and environmental impact

BackgroundAsphalt road paving and its subsequent complex airborne emissions have raised concerns about occupational exposures and environmental impacts. Although several studies described bitumen fumes or Polycyclic Aromatic Hydrocarbons (PAH) emissions at specific worksites, no comprehensive studies have characterised road paving emissions and identified the main determinants of exposure. MethodsA 10-year study from 2012 to 2022 was performed to examine the pollutants resulting from bitumen fume emissions and covering the main processes used in road paving (asphalt production, mechanical rolled asphalt paving, manual paving, mastic asphalt paving, emulsion paving, and coal-tar asphalt milling). A total of 623 air samples were collected at 63 worksites (on 290 workers, in the environment and near emission sources), and bitumen fumes, PAHs, aldehydes and volatile organic compounds were analysed. Biomonitoring campaigns were performed on 130 workers to assess internal exposure to PAHs. ResultsFume emissions revealed complex mixtures of C10–C30 compounds, including linear saturated hydrocarbons (C6–C12), alicyclic hydrocarbons and aliphatic ketones. PAHs were dominated by 2–3 aromatic ring compounds (naphthalene, fluorene, and phenanthrene), and C1–C13 aldehydes were identified. Binder proportion, paving temperature, outdoor temperature, workload and job category influenced airborne concentrations. A significant temporal trend was observed over the time period of the study, with decreasing BF and PAH exposures. PAH biomonitoring was consistent with air samples, and urinary metabolites of 2–3 ring PAHs dominated over 4–5 ring PAHs. Occupational exposures were generally far lower than exposure limits, except coal-tar asphalt milling activities. Very low environmental concentrations were measured, which highlights a negligible contribution of paving emissions to global environmental pollution. ConclusionThe present study confirmed the complex nature of bitumen fumes and characterised the main determinants of exposure. The results highlight the need to reduce the paving temperature and binder proportion. Recycled asphalt pavement use was not associated with higher emissions. The impact of paving activities on environmental airborne pollution was deemed negligible.