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Biomass burning is a significant anthropogenic source of air pollution, including the preharvest burning of sugar cane. These burn events result in atmospheric emissions, including semivolatile organic compounds, that may have adverse impacts on air quality and human health on a local, regional, and even a global scale. Gaseous and particulate polycyclic aromatic hydrocarbon (PAH) emissions from various sugar cane burn events in the province of Kwa-Zulu Natal in South Africa were simultaneously sampled using a portable denuder sampling technology, consisting of a quartz fiber filter sandwiched between two polydimethylsiloxane multichannel traps. Total gas and particle phase PAH concentrations ranged from 0.05 to 9.85 µg m -3 per individual burn event, and nine PAHs were quantified. Over 85% of all PAHs were found to exist in the gas phase, with smaller two- and three-ring PAHs, primarily naphthalene, 1-methyl naphthalene, and acenaphthylene, being the most dominant and causing the majority of variance between the burn sites. The PAH profiles differed between the different burn events at different sites, emphasizing the significant influence that the crop variety, prevailing weather conditions, and geographical location has on the type and number of pollutants emitted. The potential carcinogenicity of the PAH exposure was estimated based on toxic equivalency factors that showed varying risk potentials per burn event, with the highest value of 5.97 ng m -3 . Environ Toxicol Chem 2023;42:778-792. © 2023 The Authors. Environmental Toxicology and Chemistry published by Wiley Periodicals LLC on behalf of SETAC., (© 2023 The Authors. Environmental Toxicology and Chemistry published by Wiley Periodicals LLC on behalf of SETAC.)

The United States Environmental Protection Agency categorized polycyclic aromatic hydrocarbons (PAHs) as hazardous to humans upon acute and/or chronic exposure. This study investigated the simultaneous adsorption of several PAHs onto graphene wool (GW), thereby providing holistic insights into the competitive adsorption of PAHs onto graphene-based materials. SEM, TEM and FTIR provided evidence for the adsorption of PAHs and successful regeneration of the adsorbent accompanied by distinct morphological changes. Isotherm experiments revealed that adsorption of PAHs was significantly influenced by hydrophobic interactions between the sorbate and hydrophobic surface of GW. The Freundlich multilayer isotherm model best fit the experimental data obtained for both multi-component PAH and single-solute experiments as indicated by the Error Sum of Squares (SSE) obtained from nonlinear regression analysis. Experiments revealed that competitive adsorption had a limiting effect on the overall adsorption capacity as q max and K d were higher in single-solute than multi-component PAH experiments. The results suggest that partition distribution coefficients ( K d ) between the solid-liquid interphase played a significant role in the overall adsorption and a positive correlation between K d and Log K ow of PAHs was established in single-solute experiments. Sorption-desorption experiments revealed that PAHs were adsorbed with a maximum removal efficiency of 100% at an optimum GW dosage of 2 g/L. Adsorption thermodynamics revealed that PAH adsorption onto GW is spontaneous and endothermic. The adsorbent was regenerated and reused for up to six times and its efficiency remained fairly constant.

In the last two decades, environmental experts have focused on the development of several biological, chemical, physical, and thermal methods/technologies for remediation of PAH-polluted water. Some of the findings have been applied to field-scale treatment, while others have remained as prototypes and semi-pilot studies. Existing treatment options include extraction, chemical oxidation, bioremediation, photocatalytic degradation, and adsorption (employing adsorbents such as biomass derivatives, geosorbents, zeolites, mesoporous silica, polymers, nanocomposites, and graphene-based materials). Electrokinetic remediation, advanced phytoremediation, green nanoremediation, enhanced remediation using biocatalysts, and integrated approaches are still at the developmental stage and hold great potential. Water is an essential component of the ecosystem and highly susceptible to PAH contamination due to crude oil exploration and spillage, and improper municipal and industrial waste management, yet comprehensive reviews on PAH remediation are only available for contaminated soils, despite the several treatment methods developed for the remediation of PAH-polluted water. This review seeks to provide a comprehensive overview of existing and emerging methods/technologies, in order to bridge information gaps toward ensuring a green and sustainable remedial approach for PAH-contaminated aqueous systems. PRACTITIONER POINTS: Comprehensive review of existing and emerging technologies for remediation of PAH-polluted water. Factors influencing efficiency of various methods, challenges and merits were discussed. Green nano-adsorbents, nano-oxidants and bio/phytoremediation are desirous for ecofriendly and economical PAH remediation. Adoption of an integrated approach for the efficient and sustainable remediation of PAH-contaminated water is recommended., (© 2020 Water Environment Federation.)

In developing countries, household energy use is highly variable and complex, yet emissions arising from fuel combustion indoors are typically poorly quantified. Polycyclic aromatic hydrocarbons (PAHs) are emitted during the combustion of organic fuels such as charcoal and biomass. In the present study, multichannel polydimethylsiloxane rubber traps were used for gas-phase PAH sampling and extracted using a low-solvent volume plunger-assisted solvent extraction method. Sixteen US Environmental Protection Agency priority PAHs, primarily in the gas phase, were investigated in indoor air of rural and urban residential homes in coastal Kenya (Mombasa and Taita Taveta Counties) using typical combustion devices of each area. Average gaseous PAH concentrations per household were higher in rural (ranging 0.81-6.09 µg m -3 ) compared to urban (ranging 0-2.59 µg m -3 ) homes, although ambient PAH concentrations were higher in urban environments, likely attributable to traffic contributions. The impact of fuel choice and thereby combustion device on PAH emissions was very clear, with the highest concentrations of PAHs quantified from wood-burning emissions from 3-stone stoves (total PAH averages 46.23 ± 3.24 µg m -3 [n = 6]). Average benzo[a]pyrene equivalent total concentrations were evaluated for the priority PAHs and ranged from not detected to 43.31, 88.38, 309.61, and 453.88 ng m -3 for gas, kerosene, jiko, 3-stone, and improved 3-stone stoves, respectively. Environ Toxicol Chem 2020;39:538-547. © 2019 SETAC., (© 2019 SETAC.)

A novel graphene wool (GW) material was used as adsorbent for the removal of phenanthrene (PHEN) and pyrene (PYR) from aqueous solution. Adsorption kinetics, adsorption isotherms, thermodynamics of adsorption and effect of pH, ionic strength, and temperature on the adsorption of PHEN and PYR onto GW were comprehensively investigated. Isothermal and kinetic experimental data were fitted to Langmuir, Freundlich, Temkin, Sips and Dubinin-Radushkevich models, as well as pseudo-first-order and pseudo-second-order kinetic models. The adsorption kinetic data best fit the pseudo-second-order kinetic model for PHEN and PYR sorption with R 2 value >0.999, whilst the Sips model best fit isotherm data. Kinetic data revealed that 24 hr of contact between adsorbent and polycyclic aromatic hydrocarbons (PAHs) was sufficient for maximum adsorption, where the Langmuir maximum adsorption capacity of GW for PHEN and PYR was 5 and 20 mg g -1 and the optimum removal efficiency was 99.9% and 99.1%, respectively. Thermodynamic experiments revealed that adsorption processes were endothermic and spontaneous. Desorption experiments indicated that irreversible sorption occurred with a hysteresis index greater that zero for both PAHs. The high adsorption capacity and potential reusability of GW makes it a very attractive material for removal of hydrophobic organic micro-pollutants from water.

Lichens are useful biomonitors for atmospheric polycyclic aromatic hydrocarbons (PAHs). Different sample preparation techniques were explored in this regard, including ultrasound-assisted solvent extraction, microwave-assisted extraction, Soxhlet, and the quick, easy, cheap, effective, rugged, and safe (QuEChERS) technique. It was found that a QuEChERS technique using hexane:acetone (1:1, v/v), never reported before for application to lichens, provided the best recoveries of internal standards, the highest total peak area for all PAHs of interest, and %RSDs comparable with the other preparation techniques tested. The optimized sample preparation technique was found to be a comparatively fast method (45 min), with good recoveries (96%), using less solvents and minimal energy consumption. Strong matrix effects were found: both strong enhancement (for the lighter PAHs) and strong suppression (for the heavier PAHs). The use of matrix-matched standards is thus imperative for the accurate determination of PAH concentrations in the lichen samples. Graphical abstract "Note: This data is mandatory. Please provide."

A plunger assisted solvent extraction (PASE) method for multi-channel silicone rubber trap samplers was developed and evaluated as an alternative to direct thermal desorption for the monitoring of polycyclic aromatic hydrocarbons (PAHs). The proposed extraction method was simple, fast (a total of 2 min for extraction), and used a small volume of solvent (a total of 2 mL from two sequential 1 mL extractions). The PASE method presented an advantage over thermal desorption in that samples could be re-analyzed, as only a portion of the extract was injected. Additionally, this approach is cost effective and can be applied in laboratories which do not have thermal desorption systems, hence allowing for the more widespread use of the polydimethylsiloxane samplers which can be employed as denuders in the monitoring of gas and particle partitioning of air pollutants. The method was validated over a wide concentration range (0.005-10 ng μL -1 ) and the limits of detection ranged from 13.6 ng m -3 for naphthalene to 227.1 ng m -3 for indeno[1,2,3-cd]pyrene. Overall extraction efficiencies of the target PAHs were good (from 76% for naphthalene to 99% for phenanthrene) with relative standard deviations below 6%. The PASE method was successfully applied to the analysis of domestic fire air emission samples taken at 10 and 20 min after ignition, using a sampling flow rate of 500 mL min -1 for 10 min in each case. The samples were found to contain primarily naphthalene (maximum concentration of 9.5 μg m -3 , 10 min after ignition), as well as fluorene, anthracene, phenanthrene, fluoranthene and pyrene., (Copyright © 2018 Elsevier B.V. All rights reserved.)

Environmental pollutants, such as the polycyclic aromatic hydrocarbons (PAHs), become widely distributed in the environment after emission from a range of sources, and they have potential biological effects, including toxicity and carcinogenity. In this work, we have demonstrated the analytical potential of a covalently linked L-cysteine-capped CdSeTe/ZnSe/ZnS core/shell/shell quantum dot (QD)-graphene oxide (GO) nanocomposite fluorescence probe to detect PAH compounds in aqueous solution. Water-soluble L-cysteine-capped CdSeTe/ZnSe/ZnS QDs were synthesized for the first time and were covalently bonded to GO. The fluorescence of the QD-GO nanocomposite was enhanced relative to the unconjugated QDs. Various techniques including TEM, SEM, HRSEM, XRD, Raman, FT-IR, UV/vis and fluorescence spectrophotometry were employed to characterize both the QDs and the QD-GO nanocomposite. Four commonly found priority PAH analytes namely; phenanthrene (Phe), anthracene (Ant), pyrene (Py) and naphthalene (Naph), were tested and it was found that each of the PAH analytes enhanced the fluorescence of the QD-GO probe. Phe was selected for further studies as the PL enhancement was significantly greater for this PAH. A limit of detection (LOD) of 0.19 µg/L was obtained for Phe under optimum conditions, whilst the LOD of Ant, Py and Naph were estimated to be ~0.26 µg/L. The fluorescence detection mechanism is proposed., (Copyright © 2015 Elsevier B.V. All rights reserved.)

A novel analytical method for atmospheric polycyclic aromatic hydrocarbons (PAHs) was developed based on laser induced fluorescence (LIF) of samples on quartz multi-channel polydimethylsiloxane traps. A tunable dye laser with a frequency doubling crystal provided the excitation radiation, and a double monochromator with a photomultiplier tube detected emitted fluorescence. The method allowed for the rapid (<5 min), cost effective analysis of samples. Those yielding interesting results could be further analysed by direct thermal desorption-gas chromatography-mass spectrometry (TD-GC-MS, with limits of detection of approximately 0.3 ng m(-3)), as photodegradation was minimal (<10% over 5 min irradiation). Small amounts of naphthalene photodegradation products identified by TD-GC-MS after >15 min irradiation, included phenol, benzyl alcohol and phthalic anhydride. Without any signal optimization, a LIF detection limit of approximately 1 microg m(-3) was established for naphthalene using a diffusion tube (diffusion rate of 2 ng s(-1)) and 292 nm excitation.

Abstract: Atmospheric polycyclic aromatic hydrocarbons are ubiquitous environmental pollutants, which may be present both in the gaseous phase and adsorbed onto the surface of particles. Denuders are sampling devices which have been effectively employed in such partitioning applications. Here we describe and characterise a novel miniature denuder consisting of two multi-channel silicone rubber traps (each 178mm long, 6mm o.d. containing 22 silicone tubes), separated by a quartz fibre filter for particle phase collection. The denuder only requires a small portable personal sampling pump to provide sampling flow rates of ∼0.5Lmin−1. Theoretical considerations indicated that the air flow through the denuder was expected to be laminar, and the linear velocity arising from longitudinal diffusion was found to be negligible. The calculated particle transmission efficiency through the denuder was found to be essentially 100% for particles>50nm, whilst the experimental overall efficiency, as determined by CPC and SMPS measurements, was 92±4%. The size resolved transmission efficiency was <60% for particles below 20nm and 100% for particles larger than 200nm. Losses could have been due to diffusion and electrostatic effects. Semi-volatile gaseous analytes are pre-concentrated in the silicone of the trap and may be thermally desorbed using a commercially available desorber, allowing for total transfer and detection of the collected analytes by GC–MS. This enhances detection limits and allows for lower sampling flow rates and shorter sampling times, which are advantageous for studies requiring high temporal resolution. [Copyright &y& Elsevier]