High Molecular Weight Polycyclic Aromatic Hydrocarbons Research Articles

Northern Norway paleofire records reveal two distinct phases of early human impacts on fire activity

Paleofire records document fire’s response to climate, ecosystem changes, and human-activity, offering insights into climate-fire-human relationships and the potential response of fire to anthropogenic climate change. We present three new lake sediment PAH records and a charcoal record from the Lofoten Islands, Norway to evaluate the Holocene fire history of northern Norway and examine human impacts on fire in this region. All three datasets show an increase in PAH accumulation rate over the past c. 7500 cal years BP, with an increase c. 5000 cal years BP that signals initial human impacts on fire activity. More significant increases c. 3500 cal years BP reach a maximum c. 2000 cal years BP that correlates with the establishment and expansion of agricultural settlements in Lofoten during the Late Bronze Age and Pre-Roman Iron Age. Decreased PAH accumulation rates c. 1500–900 cal years BP reflect less burning during the Late Iron Age and early medieval period. A shift toward higher molecular weight PAHs and increasing PAHs overall from c. 1000 cal years BP to present, reflects intensified human activity. Sedimentary charcoal (>125 and 63–125 µm) in the Lauvdalsvatnet record does not vary until an increase in the last 900 years, showing a proxy insensitivity to human-caused fire. The Late-Holocene increase in fire activity in Lofoten follows trends in regional charcoal records, but exhibits two distinct phases of increased fire that reflect the intensity of burning due to human landscape changes that overwhelm the signal of natural variations in regional fire activity.

Polycyclic Aromatic Hydrocarbons in Soil and Vegetation of Niger Delta, Nigeria: Ecological Risk Assessment.

The Niger Delta, Nigeria, is noted for crude oil exploration. Whereas there seems to be a handful of data on soil polycyclic aromatic hydrocarbon (PAH) levels in this area, there is a paucity of studies that have evaluated soil and vegetation PAHs simultaneously. The present study has addressed this information gap. Fresh Panicum maximum (Jacq) (guinea grass), Pennisetum purpureum Schumach (elephant grass), Zea mays (L.) (maize), and soil samples were collected in triplicate from Choba, Khana, Trans-Amadi, Eleme, Uyo, and Yenagoa. PAHs determination was carried out using GC-MS. The percentage composition of the molecular weight distribution of PAHs, the molecular ratio of selected PAHs for identification of possible sources, and the isomeric ratio and total index of soil were evaluated. Pennisetum purpureum Schumach (elephant grass) from Uyo has the highest (10.0 mg·kg-1) PAH while Panicum maximum (Jacq) (guinea grass) has the highest PAH (32.5 mg·kg-1 from Khana. Zea mays (L.) (maize) from Uyo (46.04%), Pennisetum purpureum Schumach (elephant grass) from Trans-Amadi (47.7%), guinea grass from Eleme (49.2%), and elephant grass from Choba (39.9%) contained the highest percentage of high molecular weight (HMW) PAHs. Soil samples from Yenagoa (53.5%) and Khana (55.3%) showed the highest percentage of HMW PAHs. The total index ranged 0.27-12.4 in Uyo, 0.29-8.69 in Choba, 0.02-10.1 in Khana, 0.01-5.53 in Yenagoa, 0.21-9.52 in Eleme, and 0.13-8.96 in Trans-Amadi. The presence of HMW PAHs and molecular diagnostic ratios suggest PAH pollution from pyrogenic and petrogenic sources. Some soils in the Niger Delta show RQ(NCs) values higher than 800 and require remediation to forestall ecohealth consequences.

N-Alkanes and PAHs baseline distributions and sources in the sediments of the Nile Delta coast of the southeastern Mediterranean

The variations in the levels of n-alkanes and Polycyclic Aromatic Hydrocarbons (PAHs) in the sediment of the Nile Delta coast and extended to Bardaweel Lagoon along the Mediterranean were investigated during September 2021. The total n-alkane concentrations in the sediment samples ranged from 18.85 to 164.37 μg/g with an average value of 51.98 ± 17.49 μg/g. Similarly, the ΣPAHs concentrations ranged between 4.55 and 207.48 ng/g with an average of 27.89 ± 49.82 ng/g. The carbon preference index (CPI) values were in the 0.21 to 1.39 range, indicating variations in the sources of n-alkane at the analyzed locations. The mean carbon number (MCN) values ranged from 7.41 to 15.47, with an average of 13.34 ± 1.69. The levels of both low and high molecular weight PAHs were lower than the median and low effective range values (ERM and ERL). The computed total TEQ value varied from 0.102 to 4.129 ng/g in the sediment samples under investigation.

Anaerobic biodegradation of pyrene and benzo[a]pyrene by a new sulfate-reducing Desulforamulus aquiferis strain DSA

The study of anaerobic high molecular weight polycyclic aromatic hydrocarbons (HMW-PAHs) biodegradation under sulfate-reducing conditions by microorganisms, including microbial species responsible for biodegradation and relative metabolic processes, remains in its infancy. Here, we found that a new sulfate-reducer, designated as Desulforamulus aquiferis strain DSA, could biodegrade pyrene and benzo[a]pyrene (two kinds of HMW-PAHs) coupled with the reduction of sulfate to sulfide. Interestingly, strain DSA could simultaneously biodegrade pyrene and benzo[a]pyrene when they co-existed in culture. Additionally, the metabolic processes for anaerobic pyrene and benzo[a]pyrene biodegradation by strain DSA were newly proposed in this study based on the detection of intermediates, quantum chemical calculations and analyses of the genome and RTqPCR. The initial activation step for anaerobic pyrene and benzo[a]pyrene biodegradation by strain DSA was identified as the formation of pyrene-2-carboxylic acid and benzo[a]pyrene-11-carboxylic acid by carboxylation Thereafter, CoA ligase, ring reduction through hydrogenation, and ring cracking occurred, and short-chain fatty acids and carbon dioxide were identified as the final products. Additionally, DSA could also utilize benzene, naphthalene, anthracene, phenanthrene, and benz[a]anthracene as carbon sources. Our study can provide new guidance for the anaerobic HMW-PAHs biodegradation under sulfate-reducing conditions.

Main factors in polycyclic aromatic hydrocarbons accumulations in the long-term technogenic contaminated soil

The PAHs transformation in the soils of the coal mining enterprises impact zones and thermal power plants remains poorly studied. In turn, coal mining can be considered as a primary cycle in the production of electricity. One of the main sources of negative environmental impact is the coal mining industry located on the territory of the upland in the south of the East European Plain. The features of PAHs accumulation in the soils of fuel and energy enterprises have been studied on the example of mines impact zones with different service life and the current coal-fired power plant. It was established that, regardless of the period and intensity of the emission source, as well as its current status, the polycyclic aromatic hydrocarbons (PAHs) content in the soils of the impact zones was significantly higher than in the soils of the background territory. The content of low molecular and high molecular weight PAHs in the impact zones soils differed depending on the land use type, as well as the period and intensity of an industrial effect type. The pollutants content of in the soils of all considered impact zones significantly exceeded the background values and according to the low molecular weight PAHs content in the soils, they formed the following decreasing series: Mayskiy ≥ Ayutinsky > Novoshahtinsk > Power station > Background. According the high molecular weight PAHs content, the series changed to: Novoshahtinsk >Mayskiy ≥ Ayutinsky > Power station > Background. Soil pollution markers for enterprises of the fuel and energy complex were identified as pyrene and chrysene, which are part of coal, formed from the hydrocarbon sources. The influence of the power plant was accompanied by the benzo(g,h,i)perylene concentration increase.

Polycyclic Aromatic Hydrocarbons in Topsoils Along the Taipu River Banks in the Yangtze River Delta, China: Occurrence, Source and Risk Assessment.

Taipu River is an important transboundary river and drinking water source in the Yangtze River Delta, China. This study collected 15 topsoil samples along the Taipu River banks and subsequently determined the polycyclic aromatic hydrocarbons (PAHs) concentrations, sources, and ecological and health risks. The sum of toxic 15 PAHs concentrations ranged from 83.13 to 28342.53 ng/g, with a mean of 2828.69 ng/g. High molecular weight (HMW) PAHs were the dominant components and Indene (1,2,3, -cd) benzopyrene (InP) accounted for the highest proportion in individuals. The average PAH concentration in residential land was the highest, followed by those in industrial and agricultural land. The PAH concentration was positively related to contents of total carbon, total nitrogen, ammonium nitrogen, and aminopeptidase activity in soils. The mixed combustion of biomass, coal, and petroleum and traffic emissions could be the primary PAH contributors. The total PAHs at over half of sampling points had relatively high risk quotients and incremental lifetime cancer risk (ILCR) values, posing potential or great ecological threats and health risks.

Comprehensive study on particle size distribution, MAH and PAH profiles during alkylbenzene pyrolysis

The 5 linear alkylbenzenes, i.e., toluene, ethylbenzene, n-propylbenzene, n-butylbenzene, and n-pentylbenzene as fuels underwent pyrolysis at temperatures from 950 to 1450 °C in a flow reactor. Measurements of particle number size distribution, 11 monocyclic aromatic hydrocarbons, and 3 groups of polycyclic aromatic hydrocarbons (20 unsubstituted PAHs, 5 aliphatic-bridged PAHs, and 10 methyl PAHs) during the pyrolysis of linear alkylbenzenes were conducted. Results showed that the increase in side chain length suppressed the formation of particles, but ethylbenzene produced the highest particle mass and most extensive particle number size distribution. Total particle peak number concentrations exhibited a rise-then-fall trend (peaking at a critical temperature of 1050 °C) with increasing temperature regardless of the side chain length, indicating that high temperature promoted a transition from nucleation to agglomeration and coagulation. Total PAH mass concentrations were ranked in the same order with the variation of side-chain length as particle mass and peak number concentrations, indicating that soot nucleation was highly related to total PAH mass concentrations. Unsubstituted PAHs accounted for most PAHs while substituted·PAHs, including aliphatic-bridged PAHs and methyl PAHs presented 1–2 orders of magnitude less than the corresponding unsubstituted PAHs, probably distinct thermal stability and reactivity led to different growth routes between unsubstituted and substituted PAHs. Increasing the temperature from 950 to 1250 °C, the formation of high molecular weight PAHs was promoted. while a drop of high molecular weight fractions was observed above 1350 °C, which is attributed to the suppression of the formation, as well as their conversions of high molecular weight PAHs to heavier unidentified PAHs or soot. Among the test alkylbenzene fuels, the fuels with a long side chain benefit from the reduction of particles and PAHs. Furthermore, carbon atoms in aromatic rings are dominant sources of large PAHs and particles, while the carbon atoms in aliphatic side chains mainly form gas species.

Cometabolic degradation of pyrene with phenanthrene as substrate: assisted by halophilic Pseudomonas stutzeri DJP1.

At present, cometabolic degradation is an extensive method for the biological removal of high molecular weight polycyclic aromatic hydrocarbons (HMW-PAHs) in the marine environment. However, due to the refractory to degradation and high toxicity, there are few studies on pyrene (PYR) cometabolic degradation with phenanthrene (PHE) as substrate. In this study, a Pseudomonas stutzeri DJP1 strain isolated from sediments was used in the cometabolic system of PHE and PYR. The biomass and the activity of key enzymes such as dehydrogenase and catechol 12 dioxygenase of strain were improved, but the enhancement of biotoxicity resulted in the inhibition of cometabolism simultaneously. Seven metabolites were identified respectively in PYR, PHE degradation cultures. It was speculated that the cometabolism of PHE and PYR had a common phthalic acid pathway, and the degradation pathway of PHE was included in the downstream pathway of PYR. The functional genes such as PhdF, NidD and CatA involved in DJP1 degradation were revealed by Genome analysis. This study provides a reference for the biodegradation of PYR and PHE in real marine environment.

Assessment of polycyclic aromatic hydrocarbons (PAHs) in mediterranean top marine predators stranded in SE Spain

Polycyclic aromatic hydrocarbons (PAHs) are ubiquitous environmental pollutants. Although they are not bioaccumulated in vertebrates, chronic exposures might still derive on serious toxic effects. We studied concentrations of 16 reference PAHs on blubber of two dolphin species (striped dolphin, n = 34; and bottlenose dolphin, n = 8) and one marine turtle (loggerhead turtle, n = 23) from the Mediterranean waters of SE Spain, an important or potential breeding area for these and other related species. Σ16 PAHs concentrations were relatively similar between the three species, but they were in the lower range in comparison to worldwide data. Of the six PAHs detected, fluoranthene was the only high molecular weight (HMW) PAH, so low molecular weight (LMW) PAHs predominated. Naphthalene and phenanthrene were invariably those PAHs with higher detection rates as well as those with higher concentrations. In accordance with the literature, sex and length did not have significant influence on PAHs concentrations, probably due to high metabolization rates which prevent for observation of such patterns. Despite LMW PAHs are considered less toxic, we cannot dismiss toxic effects. This is the first work assessing PAHs concentrations in cetaceans and sea turtles from the SE Spain, which could serve as the baseline for future research.

Occurrence, sources, and ecological risks of polycyclic aromatic hydrocarbons (PAHs) in the Amazon river

The Amazon is the largest river by discharge volume and one of the most biodiverse biomes in the world. Lately, there has been a rapid increase of the urban population in the region, which has been translated into a growing emission of organic contaminants such as polycyclic aromatic hydrocarbons (PAHs) into surface water bodies. This study provides the most comprehensive evaluation of the PAH contamination levels in surface waters of the Amazon basin. We investigated the occurrence and potential sources of 16 priority PAHs and characterised their risks for freshwater ecosystems. For this, we took 40 water samples from different sites along the Brazilian part of the Amazon River, including three major tributaries, and smaller rivers crossing the main urban areas. The results of this study show that PAHs are widespread contaminants in rivers of the Brazilian Amazon. The sum of the total concentration of the 16 priority PAHs reached values of 134 ng L−1 in the Amazon River, and 163 ng L−1 near densely populated areas. On the other hand, the total PAH concentration was generally lower in the monitored tributaries. In most samples, the contamination pattern was dominated by high molecular weight PAHs, suggesting a major contribution of pyrogenic sources, although petrogenic contamination was also present in some locations near urban areas. We assessed ecological risks posed by PAH mixtures using a hazard index. The results indicated that PAH contamination is not likely to pose direct toxic effects for Amazonian freshwater organisms, however continued monitoring is recommended near densely populated areas.

PM2.5/PM10-bound PAHs in Hotan city: Concentrations, sources, and contribution to ·OH

The air pollution in Hotan, Xinjiang is serious and the high concentration of polycyclic aromatic hydrocarbons (PAHs) cannot be ignored. Studies on the characteristics of PAHs in the region are still limited. In this paper, PM10 and PM2.5 samples were collected from the urban area of Hotan in summer and winter, and the concentrations, sources and contributions to hydroxyl radicals (·OH) of 12 PAHs were analyzed. The mean concentrations of PM2.5/PM10-bound PAHs were much higher in winter (150 ± 38.8 ng/m3 and 156 ± 38.1 ng/m3) than in summer (6.34 ± 6.28 ng/m3 and 7.64 ± 6.75 ng/m3), with greater contributions from medium and high molecular weight PAHs. PAHs are mainly derived from vehicle emissions, coal and biomass combustion, with coal combustion making the largest contribution to ·OH concentrations. The combination of air mass trajectory clustering and potential source contribution factor analysis (PSCF) revealed that long-range transport contributed less to the PAHs content, and local domestic source emissions dominated. Studies have shown a significant positive correlation between PAHs and ·OH concentrations, indicating that PAHs are oxidatively toxic to humans. Controlling PAHs emission in winter in Hotan and reducing the concentration of PAHs in respirable particulate matter will help to reduce the damage to human health.

Historical trends of traditional, emerging, and halogenated polycyclic aromatic hydrocarbons recorded in core sediments from the coastal areas of the Yellow and Bohai seas

Historical trends of polycyclic aromatic hydrocarbons (PAHs) contamination were reconstructed from eleven sediment cores located in intertidal zones of the Yellow and Bohai seas for a period encompassing the last 80 years. The analysis encompassed 15 traditional PAHs (t-PAHs), 9 emerging PAHs (e-PAHs), and 30 halogenated PAHs (Hl-PAHs), including 10 chlorinated PAHs (Cl-PAHs) and 20 brominated PAHs (Br-PAHs). Concentrations of target PAHs were highest in industrial and municipal areas situated along the coast of the Bohai Sea, including Huludao, Yingkou, Tianjin, and Dandong, constituting a substantial mass inventory. All target PAHs showed increasing trends since the 1950s, reflecting the development history of South Korea and China. High molecular weight PAHs accumulated in sampling sites more than low molecular weight PAHs. A positive matrix factorization model showed that the PAH sources were coal and gasoline combustion (35%), diesel combustion (33%), and biomass combustion (32%). Over the last 80 years, the contribution of coal and gasoline combustion increased in all regions, while diesel combustion and biomass combustion varied across regions and over time. Toxicity equivalence values were highest for t-PAHs (>99% contribution), followed by Cl-PAHs, Br-PAHs, and e-PAHs. Concentrations of t-PAHs in Eastern Asia seas have increased since the 1900s, particularly in intertidal areas compared to subtidal areas. The intertidal zone removed 83% of the total flux of PAHs originating from land and thus appears to serve as a buffer zone against marine pollution. Overall, this study provides novel knowledge on the historical trends and sources of PAHs on a large scale, along with insights for future coastal management.

Polycyclic aromatic hydrocarbons in the water column of three hot spot areas, Jeddah coast, eastern of Red Sea

Jeddah coast receiving significant amount of persistent organic pollutants including polycyclic aromatic hydrocarbons (PAHs). Sources of PAHs mainly introduced to the coastal area from sewage influents, vehicle exhausts, industrial and Islamic harbor activates. In the present study, dissolved PAHs in the surface and near bottom waters were assessed in three highly polluted coastal areas in Jeddah city (Islamic Jeddah Port, Al-Arbaeen and Al-Shabab lagoons), eastern side of the Red Sea. The study aims to investigate vertical and horizontal distribution of PAHs in the water column, and explore the anthropogenic and environmental factors affecting their distribution. The total concentration of parent and methylated PAHs (∑25PAHs) in the near bottom waters were ranged between 377 and 1300 ng/L (average: 773 ± 329 ng/L), while the concentrations in surface waters (∑11PAHs) were ranged between 151 and 748 ng/L (average: 360 ± 174 ng/L). The concentrations of PAHs in the bottom waters were almost double those of surface waters. The area reached by particulate organic matter from sewage effluents that adsorbed low soluble high molecular weight PAHs from the surface waters on their way to the sediments then sediment-bottom water exchange released considerable amount of PAHs in bottom waters. The diagnostic ratios pointed out to a mixture of petrogenic and pyrogenic origins in the surface and near bottom waters. The toxic and mutagenic equivalent quotients for carcinogenic PAHs in the bottom waters were found 47 and 49 ng TEQ/L, respectively. The PAH levels in the study area indicated adverse effects are probable to occur.

Occurrence, distribution, and toxicity assessment of polycyclic aromatic hydrocarbons in biochar, biocrude, and biogas obtained from pyrolysis of agricultural residues

Occurrence, distribution, and toxicity assessment of polycyclic aromatic hydrocarbons (PAHs) in pyrolysis steams (biochar, biocrude, and biogas) of three agricultural residues was investigated at pyrolysis temperatures of 400–800 °C. Increasing PAHs formation was observed in the narrow temperature range (500–600 °C) in all feedstocks due to temperature-induced dehydration, decarboxylation, and dehydrogenation reactions. Low molecular weight PAHs (naphthalene, phenanthrene) were dominant in all product streams while high molecular weight PAHs were found in negligible concentrations. Leaching studies showed that pyrolyzed biochars produced at lower temperatures are more prone to leaching due to the presence of hydrophilic amorphous uncarbonized structures, while the presence of hydrophobic carbonized matrix with denser and stronger polymetallic complex prevents the leaching of PAHs in the high temperature pyrolyzed biochar. Low leaching potential, low toxic equivalency, and permissible total PAHs values in biochar derived from all three feedstocks warrant the broader application and ensure ecological safety.

Genotoxicity by rapeseed methyl ester and hydrogenated vegetable oil combustion exhaust products in lung epithelial (A549) cells.

Biofuel is an attractive substitute for petrodiesel because of its lower environmental footprint. For instance, the polycyclic aromatic hydrocarbons (PAH) emission per fuel energy content is lower for rapeseed methyl ester (RME) than for petrodiesel. This study assesses genotoxicity by extractable organic matter (EOM) of exhaust particles from the combustion of petrodiesel, RME, and hydrogenated vegetable oil (HVO) in lung epithelial (A549) cells. Genotoxicity was assessed as DNA strand breaks by the alkaline comet assay. EOM from the combustion of petrodiesel and RME generated the same level of DNA strand breaks based on the equal concentration of total PAH (i.e. net increases of 0.13 [95% confidence interval (CI): 0.002, 0.25, and 0.12 [95% CI: 0.01, 0.24] lesions per million base pairs, respectively). In comparison, the positive control (etoposide) generated a much higher level of DNA strand breaks (i.e. 0.84, 95% CI: 0.72, 0.97) lesions per million base pairs. Relatively low concentrations of EOM from RME and HVO combustion particles (<116 ng/ml total PAH) did not cause DNA strand breaks in A549 cells, whereas benzo[a]pyrene and PAH-rich EOM from petrodiesel combusted using low oxygen inlet concentration were genotoxic. The genotoxicity was attributed to high molecular weight PAH isomers with 5-6 rings. In summary, the results show that EOM from the combustion of petrodiesel and RME generate the same level of DNA strand breaks on an equal total PAH basis. However, the genotoxic hazard of engine exhaust from on-road vehicles is lower for RME than petrodiesel because of lower PAH emission per fuel energy content.

Occurrence and probabilistic risk assessment of polycyclic aromatic hydrocarbons in blood and urine of auto-mechanics in Akure Metro, Nigeria

This study provides baseline data on the concentration of polycyclic aromatic hydrocarbons (PAHs) in blood and urine samples of auto-mechanics, using Nigeria as a case study. Eighteen auto-mechanics participated in the study excluding two controls. The concentrations for the ΣPAHs across all participants (excluding control) ranged from 1.67 to 3.30 (2.17 ± 0.58) in blood with a significantly higher (P < 0.05) range of 7.61 to 10.76 (8.69 ± 1.00) in urine. The high molecular weight PAHs (4-6 rings) dominated the PAH profile in both blood (≥ 92%) and urine (≥ 87%) across all locations. Dibenz(a)anthracene was the most distributed PAH, while acenaphthene and indeno(1,2,3-cd)pyrene were the least distributed. The dermal route constituted approximately 99% of the total chronic exposure, followed by ingestion, and the least via inhalation. The hazard index (HI) was below the safe thresholds (HI = 1), suggesting non-carcinogenic PAH effects. However, all the participants including control samples had carcinogenic risk (CR) values above the acceptable level of 10-6 in both blood and urine samples. The carcinogenic and mutagenic potencies were higher in urine than in blood. The results suggest less acute toxicity and more potential chronic effects. The computed elimination ratio (> 1) suggests low excretion in urine and a potentially harmful trend. Molecular diagnostic ratios and principal component analysis suggest mixed PAH sources. The study revealed biomonitoring solely dependent on blood analysis may greatly underestimate health risks due to PAH exposure. To the best of our knowledge, this study is the first to provide levels of PAHs in the blood and urine of Nigerian mechanics. Findings herein will support policymakers at all levels in re-focusing attention to the less prioritized professions that pre-disposes people to PAHs and other emerging pollutants in society.

Evaluating the performance of surfactant and charcoal-based cleaning products to effectively remove PAHs from firefighter gear

Firefighters regularly respond to fire scenes where a mixture of chemicals including volatile, semi-volatile, and nonvolatile compounds are present in smoke and soot. Polycyclic aromatic hydrocarbons (PAHs) are common contaminants at fire scenes that may be deposited on the gear and the individual firefighter. Laundering is a common approach for the decontamination of contaminated gear. Surfactants are widely used by firefighters during laundering to remove PAHs as they are generally non-toxic and biodegradable. The removal of PAHs depends on the surfactant types, chemistries, and concentrations. This study evaluated the effect of surfactant concentrations to remove persistent contaminants like PAHs from turnout gear. The cleaning performance of different types of surfactants was also evaluated. Outer shell fabrics were contaminated with a standard mixture of 16 PAH compounds, and two commercial detergents were used at different concentrations. Additionally, the cleaning efficacy of eight commercially available regular and charcoal-based cleaning products was also determined against PAHs at a single surfactant concentration. For the decontamination method, a bench-scale washing procedure simulating the National Fire Protection Assocation 1851 laundering process was used. The removal efficacy of high molecular weight (HMW) PAHs were found to be lower compared to the low molecular weight PAHs for any type or any concentration of detergent. Our research also showed that the recommended surfactant concentrations provided by detergent manufacturers can be ineffective at removing the HMW PAHs from heavily contaminated fabric. With 1 mL of detergent in a 100-mL bath, which is multiple times higher than recommended amount, only 40% of HMW PAHs were removed. The cleaning efficacy can be increased to above 90% by using higher concentrations of detergents. This research shows that firefighters may need to use a higher concentration of detergent than the recommended amount to effectively remove PAHs from the gear. All the regular and charcoal-based detergents were able to remove PAHs effectively from contaminated fabrics when a higher concentration of detergent was used.

Bioengineering remediation of former industrial sites contaminated with chemical mixtures

Former gasworks sites are known to be contaminated with complex chemical mixtures that require remediation before redevelopment. Bioamendments such as biochar and spent mushroom compost (SMC) offer a green and sustainable remediation approach to help tackle this issue. However, the effectiveness of different biochar types and their interactions with the soil microbial community is still not well understood. To address this, a full factorial microcosm experiment was carried out using biochar derived from rice husk (RHB) and wheat straw (WSB) mixed with soil from a former gasworks site at varying concentrations (0%, 2.5%, and 5%), with and without SMC. The experiment aimed to evaluate the fate of contaminants including alkanes, PAHs, and metals, and their effect on the soil microbial community, as well as the implications for remediation endpoints. The results showed that the bioamendments had an average TPH reduction of 92%, with SMC and WSB-SMC having the highest degradation rates at 93%. While the bioamendments did not significantly affect the extent of TPH removal compared to the control, they did improve the degradation of high molecular weight (HMW) PAHs, particularly in RHB-SMC for EC17-20 (60%) and EC21-35 (62%) of total PAH concentration, and in WSB-SMC for HMW bioavailable PAH concentration (89%). The bioamendments also affected the partitioning and distribution of metals after 120 days of treatment, leading to decreased available phase fractions. The treatments increased microbial abundance in the soil, with Gram positives, Gram negatives, and fungi increasing by 4%, 8%, and 38%, respectively, after 120 days, particularly in SMC and mixed treatments. This was mirrored in increased microbial soil respiration. After 120 days, low metal (178 ± 5 mg/kg) and TPH (21 ± 7 mg/kg) bioavailability translated into higher EC50 (10624 ± 710 mg/L), indicating lower toxicity. There was a strong correlation between bioavailability and toxicity of TPH and metals with microbial relative abundance and activity. In summary, while green and sustainable remediation may accelerate the remediation process, monitored natural attenuation may be sufficient for site reclamation. However, this strategy, as demonstrated here, can reduce metal bioavailability, and promote the biodegradation of HMW PAHs.

Contrasting response strategies of microbial functional traits to polycyclic aromatic hydrocarbons contamination under aerobic and anaerobic conditions

PAHs (Polycyclic aromatic hydrocarbons) are widely distributed in soil ecosystems, but our knowledge regarding the impacts of PAHs effects on soil microbial functional traits is limited. In this study, we evaluated the response and regulating strategies of microbial functional traits that are associated with the typical C, N, P, S cycling processes in a pristine soil under aerobic and anaerobic conditions after the addition of PAHs. Results revealed that indigenous microorganisms had strong degradation potential and adaptability to PAHs especially under aerobic conditions, while anaerobic conditions favored the degradation of high molecular weight PAHs. PAHs exhibited contrasting effects on soil microbial functional traits under different aeration conditions. It would probably change microbial carbon source utilization preference, stimulate inorganic P solubilization and strengthen the functional interactions between soil microorganisms under aerobic conditions, while might cause the increase of H2S and CH4 emissions under anaerobic conditions. This research provides an effective theoretical support for the ecological risk assessment of soil PAHs pollution.

Assessment of entrainment of key PAHs emanating from major combustion sources into the ambient air

Increasing health problems owing to air pollution is the major cause of concern in the present time, especially in regions with exceptionally high particulate matter (PM) namely Indo-Gangetic Plains (IGP). In the ambient PM, polycyclic aromatic hydrocarbons (PAHs) have been reported to be carcinogenic in nature and its dominant sources are diesel emissions, coal combustion, agricultural waste burning, wood, and cow-dung cake burning. The chemical characteristics of particulate-bound PAHs from all the mentioned sources, their intercomparison, and entrainment into the atmosphere have been assessed in this study. High-molecular weight (HMW) PAHs fraction is highest in emissions from coal combustion (∼95%), followed by agricultural waste burning (83%), wood burning (83%) and cow-dung cake (77%) combustion. Among all the PAH compounds, benzo (b,j) fluoranthene (B[bj]F) was found to be predominant (highest in wood combustion ∼20.3%) in all source samples except exhaust from diesel and bio-diesel engine installed with diesel oxidation catalyst (DOC). Dominant PAH compounds contributing to the carcinogenic potential (CP) are benzo (a) pyrene (B[a]P), dibenzo (a,h) anthracene (D[ah]A), benzo (b,j) fluoranthene (B[bj]F), benzo (a) anthracene (B[a]A) and indeno (1,2,3-c,d) pyrene (IP). Wood combustion (CP = 1.4 ± 0.8) emission is observed to be the most carcinogenic followed by coal combustion (0.8 ± 0.2), diesel exhaust emission (0.4 ± 0.3), cow-dung cake burning (0.2), and agricultural waste burning (0.2 ± 0.1). Further, the range of various diagnostic ratios for each of the source samples has been reported that can be utilized in future studies for more comprehensive source apportionment.