Absorption Of Polycyclic Aromatic Hydrocarbons Research Articles

PAHs emissions from residential biomass burning in real-world cooking stoves in rural China

Indoor biomass burning is a major contributor to the emission of PAHs (polycyclic aromatic hydrocarbons) in China. To date, estimates of PAH emissions from the burning of biomass have involved considerable uncertainty, mostly from the lack of real-world measurements of emission factors. In this study, we conducted a comprehensive evaluation on PAH emissions from biomass burning in real-world cooking stoves in three Chinese provinces. PAH emission factors, in both particle- and gas-phase, from 11 fuel-stove combinations were measured and the provincial emissions were estimated based on the measured emission factors and fuel consumption. The measured PAH28 emission factors (including 16 US EPA priority PAHs and 12 non-priority PAHs) ranged from 42 mg/kg to 370 mg/kg, with an order of magnitude difference, which was mostly affected by fuel type. The emission factors measured in this study were generally higher than those reported in laboratory studies and were comparable with field studies. The gas-particle distribution indicated that the absorption of PAHs by organic carbon in particulate matter (PM) was the dominant sorption mechanism in gas-particle distribution. The composition profile was different from previous studies, especially for non-priority PAHs, which are highly toxic and should be given more attention. Following the disparities in composition profiles, our study suggests that source apportionment based on single- or multi-diagnostic ratios may lead to large bias and uncertainties. It appears that the toxicity potential of PAHs in northern China emitted from combustion of crop residues is greater than that in southern China where PAHs are mainly emitted from wood combustion.

Effect Of Skin Temperature On Dermal Absorption Of Anthracene

Exposure to a variety of ubiquitous pollutants, including polycyclic aromatic hydrocarbons (PAHs), occurs during daily exposure to vehicular exhaust fumes, smoking, grilling, and in many occupations, including firefighting. Dermal absorption of potential carcinogens has received limited attention compared to respiratory routes due to the challenges with measurement in vivo. PURPOSE: Our aims were 1) establish the efficacy of microdialysis (MD) as a sampling technique for dermal absorption of PAHs and 2) determine the effect of skin temperature on dermal absorption of the non-carcinogenic PAH, anthracene (ANT). METHODS: Two MD fibers were inserted into the ventral forearm of 6 healthy participants (32 ± 5 yrs, 5 male, 1 female) and perfused with lactated Ringers and 10% 2-hyroxypropyl-β-cyclodextrin at a rate of 1 μl/min. 2% ANT cream was applied over each site, dialysate samples were collected and skin blood flow (SkBF) measured at a locally heated (HT, 43°C) and thermoneutral (TN, 33°C) site. The concentration of ANT from dialysate samples were measured via targeted tandem mass spectrometry. RESULTS: Dialysate ANT concentration was similar between the HT and TN sites (2.9 ± 0.4 vs. 3.5 ± 0.4 ppm, P=0.26). Absolute SkBF was significantly higher at the HT versus TN site (35.7 ± 11.8 and 7.2 ± 1.0 CVC, P=0.001). CONCLUSIONS: These data provide support for MD as a sampling technique for dermal absorption of PAHs. Despite similar ANT concentrations between sites, dermal absorption and sampling can be modulated by multiple factors. Further research is required to elucidate the influence of skin temperature versus clearance on dermal absorption of ANT and other PAHs. This has important implications for understanding dermal absorption of potentially carcinogenic compounds in occupational workers and the general poulation.

Exposure and Absorption of PAHs in Wildland Firefighters: A Field Study with Pilot Interventions.

ObjectivesThere is limited knowledge of exposure to polycyclic aromatic hydrocarbons (PAHs) in wildland firefighters, or of the effectiveness of interventions to reduce this. This study of wildland firefighters assessed whether PAHs were present and considered respiratory protection and enhanced skin hygiene as possible interventions.Methods1-Hydroxypyrene (1-HP) was measured in urine samples collected pre-shift, post-shift, and next morning from wildland firefighters in Alberta and British Columbia. Skin wipes, collected pre- and post-shift, were analysed for eight PAHs. Breathing zone air samples were analysed for 11 PAHs. As pilot interventions, participants were randomized to either normal or enhanced skin hygiene. A sample of volunteers was assigned to a disposable N95 mask or a half facepiece mask with P100 organic vapour cartridge. Participants completed a brief questionnaire on activities post-shift and respiratory symptoms.ResultsNon-smoking firefighters (66 male and 20 female) were recruited from 11 fire crews. Air sampling pumps were carried for the full shift by 28 firefighters, 25 firefighters wore masks (14 N95 and 11 P100); 42 were assigned to the enhanced skin hygiene intervention. Sixty had hot spotting as their main task. Air monitoring identified PAHs (benzo(b,j,k)fluoranthene in particulates, phenanthrene in the gaseous phase) for 6 of the 11 crews. PAHs (largely naphthalene) were found post-shift on 40/84 skin wipes from the hand and 38/84 from jaw/throat. The mean increase in 1-HP in urine samples collected after the shift (compared with samples collected before the shift) was 66 ng g−1 creatinine (P < 0.001) with an increase over the shift found for 76% of participants. 1-HP in next morning urine samples was significantly lower than at the end of shift (a reduction of 39.3 ng g−1: P < 0.001). The amount of naphthalene on skin wipes was greater at the end of the shift (post) than at the start (pre). The mean post–pre weight difference of naphthalene on skin wipes taken from the hand was 0.96 ng wipe−1 (P = 0.01) and from the jaw/throat 1.28 ng wipe−1 (P = 0.002). The enhanced skin hygiene intervention lead to a larger reduction in 1-HP between end of shift and next morning urine samples but only for those with naphthalene on skin wipes at the end of shift. The difference in 1-HP concentration in urine samples collected before and after the shift was reduced for those wearing a mask (linear tend P = 0.063, one-sided). In multivariable models, 1-HP at end of shift was related to gaseous phase phenanthrene, estimated from air sampling [β = 318.2, 95% confidence interval (CI) 67.1–569.2]. Naphthalene on hand skin wipes reflected work in hot spotting during the shift (β = 0.53, 95% CI 0.22–0.86).ConclusionsThis study provided evidence of PAHs in the air and on the skin of many, but not all, fire crew. Absorbed PAHs, reflected in 1-HP in urine, increased over the shift. Results from the pilot interventions suggest that enhanced skin hygiene would reduce absorption post fire where PAHs had been accumulated on the skin, and that masks could be effective in reducing PAH inhalation exposure. Interventions to reduce PAH absorption are supported by the pilot work reported here and warrant further evaluation across a full fire season.

Dermal bioaccessibility and absorption of polycyclic aromatic hydrocarbons (PAHs) in indoor dust and its implication in risk assessment

Numerous studies have focused on assessing the risk of human exposure to polycyclic aromatic hydrocarbons (PAHs) in indoor dust via dermal contact. However, the dermal bioaccessibility and dermal absorption of PAHs in indoor dust have seldom been reported. In the present study, the effects of temperature, sweat ratio, solid-liquid ratio and incubation time on the dermal bioaccessibility of PAHs were examined. Naphthalene, phenanthrene, pyrene and benzo[a]pyrenewere selected for examination in an absorption assay with keratinocyte cells. The results showed the release of PAHs from indoor dust fitted a first-order one-compartment model. Naphthalene had the highest rate of release, which was consistent with the bioaccessibility assay results. In addition, the absorption rate of naphthalene and phenanthrene by keratinocytes was higher than that of pyrene and benzo[a]pyrene, with the latter being of higher molecular weight. These results indicated that low molecular weight PAHs were much more easily absorbed via dermal contact than were high molecular weight PAHs. The dermal bioavailability of PAHs in indoor dust was estimated by multiplying the bioaccessibility of PAHs in indoor dust by the ratio of dermal absorption by skin cells, and ranged from 0.12 to 51.0%. These data will be useful in risk assessments.

The absorption of polycyclic aromatic hydrocarbons into the skin to elicit cutaneous inflammation: The establishment of structure–permeation and in silico–in vitro–in vivo relationships

Polycyclic aromatic hydrocarbons (PAHs) can induce skin toxicity. Although some investigations have been conducted to assess the skin toxicity of different PAHs, few comparisons using a series of PAHs with different ring numbers and arrangements have been done. We aimed to explore the skin absorption of 6 PAH compounds and their effect on cutaneous inflammation. In vitro skin permeation was rated by Franz cell with pig skin. Molecular docking was employed to compute the PAH interaction with stratum corneum (SC) lipids. Cultured keratinocytes were exposed to PAHs for analyzing cytotoxicity, cyclooxygenase (COX)-2, prostaglandin E2 (PGE2), chemokines, and differentiation proteins. The in vivo topical PAH exposure in mice was characterized by skin absorption, transepidermal water loss (TEWL), PGE2 level, and histology. The skin deposition from the aqueous vehicle increased following the increase of PAH lipophilicity and molecular size, with benzo[a]pyrene (5-ring PAH) showing the greatest absorption. Pyrene was the compound showing the highest penetration across the skin (flux). Although the PAHs fluoranthene, pyrene, chrysene, and 1,2-benzanthracene all had 4 rings, the skin permeation was quite different. 1,2-Benzanthracene showed the greatest absorption among the 4-ring compounds. The PAHs with higher absorption exhibited stronger interaction with SC lipids according to the in silico modeling. Chrysene and 1,2-benzanthracene generally showed the highest COX-2 and PGE2 expression, followed by benzo[a]pyrene. The lowest COX-2 and PGE2 upregulation was observed for naphthalene (2-ring PAH). A contrary tendency was detected for the upregulation of chemokines. Filaggrin and integrin β1 in keratinocytes were suppressed at a comparable level by all PAHs. The skin’s absorption of PAHs showed strong in vivo–in vitro correlation. 1,2-Benzanthracene and benzo[a]pyrene highly disrupted the skin barrier and elevated the inflammation in vivo. The tendency toward in vivo inflammation caused by various PAHs could be well predicted by the combined estimation using in vitro skin absorption and a keratinocyte bioassay. This study also established the structure–permeation relationship (SPR) of PAHs.

Performance of butyl rubber-based macroporous sorbents as passive samplers.

In this study, two macroporous butyl rubber (BR)-based sorbents prepared in benzene (H-BR) and in cyclohexane (L-BR) with different porosities were synthesized by cryogelation technique. Their performances as a passive sampler were studied and then compared with commercially available silicon rubber (polydimethylsiloxane, PDMS) passive sampler. For that aim, polycyclic aromatic hydrocarbon (PAH) absorption rates of the sorbents in the short-term and their accumulation capacities in the long-term periods were investigated. Four PAHs (naphthalene, phenanthrene, fluoranthene, and pyrene) with a different number of aromatic rings were utilized. The concentrations of the PAHs in solutions were quantified by fluorescence spectrophotometer. The results showed that the BR sampler prepared in benzene (H-BR) generally has the highest absorption rates for all PAHs. The rate constants k (h-1) of the H-BR, L-BR, and PDMS samplers were found as 1.07, 0.55, and 0.55 for naphthalene; 0.73, 0.16, and 0.09 for phenanthrene; 0.24, 0.26, and 0.08 for fluoranthene; and 0.97, 0.38, and 0.17 for pyrene, respectively. The highest PAH absorption capacity was found for the BR sorbents prepared in benzene for all PAHs. Thus, benzene was selected as the organic solvent rather than cyclohexane for further studies in the preparation of butyl rubber-based samplers. The H-BR possessing the highest absorption rate and capacity underlines their usage as a capable passive sampler for both short- and long-term monitoring activities in the aquatic environments.

Modelling the absorption spectra of polycyclic aromatic hydrocarbons over Seoul, South Korea

Abstract The effects of light-absorbing atmospheric particles on climate forcing have been integrated into climate models, but the absence of brown carbon (BrC) in these models has led to differences between model predictions and measured data. Herein, we have used density functional theory (DFT) to generate models for the atmospheric absorption of polycyclic aromatic hydrocarbons (PAHs), major contributors to BrC light absorption, found over Seoul (South Korea), considering their seasonal and yearly variation. Winter was found to be the most problematic season, with significant absorption from the PAHs, while the absorption was more moderate in the autumn and in the spring. In the summer, the absorption is relatively quite weak. This is in line with the higher concentration of PAHs during winter, followed by autumn and spring, while being lower during summer. Moreover, these models showed that PAHs absorb strongly in the UVA and UVB regions of the UV spectrum, followed by moderate absorption in the UVC region and weak absorption in the visible region. Nevertheless, only absorption at the UVA and the visible region should be relevant for climate forcing. Finally, fluoranthene and benzo[a]anthracene are the most relevant contributors for UVB absorption, while benzo[a]pyrene, benzo[g,h,i]perylene, indeno[1,2,3-cd]pyrene and benzo[k]fluoranthene are the main responsible for absorption in the visible region. Thus, our modelling approach allowed us to identify which should be the most relevant PAHs for climate forcing on this region of the globe.

Firefighters' and instructors' absorption of PAHs and benzene during training exercises.

Introduction:Training fires may constitute a major portion of some firefighters’ occupational exposures to smoke. However, the magnitude and composition of those exposures are not well understood and may vary by the type of training scenario and fuels.Objectives:To understand how structure fire training contributes to firefighters’ and instructors’ select chemical exposures, we conducted biological monitoring during exercises involving combustion of pallet and straw and oriented strand board (OSB) or the use of simulated smoke.Methods:Urine was analyzed for metabolites of polycyclic aromatic hydrocarbons (PAHs) and breath was analyzed for volatile organic compounds (VOCs) including benzene.Results:Median concentrations of nearly all PAH metabolites in urine increased from pre-to 3-hr post-training for each scenario and were highest for OSB, followed by pallet and straw, and then simulated smoke. For instructors who supervised three trainings per day, median concentrations increased at each collection. A single day of OSB exercises led to a 30-fold increase in 1-hydroxypyrene for instructors, culminating in a median endof-shift concentration 3.5-fold greater than median levels measured from firefighters in a previous controlledresidential fire study. Breath concentrations of benzene increased 2 to 7-fold immediately after the training exercises (with the exception of simulated smoke training). Exposures were highest for the OSB scenario and instructors accumulated PAHs with repeated daily exercises.Conclusions:Dermal absorption likely contributed to the biological levels as the respiratory route was well protected. Training academies should consider exposure risks as well as instructional objectives when selecting training exercises.

Firefighters’ absorption of PAHs and VOCs during controlled residential fires by job assignment and fire attack tactic

To better understand the absorption of combustion byproducts during firefighting, we performed biological monitoring (breath and urine) on firefighters who responded to controlled residential fires and examined the results by job assignment and fire attack tactic. Urine was analyzed for metabolites of polycyclic aromatic hydrocarbons (PAHs) and breath was analyzed for volatile organic compounds (VOCs) including benzene. Median concentrations of PAH metabolites in urine increased from pre-firefighting to 3-h post firefighting for all job assignments. This change was greatest for firefighters assigned to attack and search with 2.3, 5.6, 3.9, and 1.4-fold median increases in pyrene, phenanthrene, naphthalene, and fluorene metabolites. Median exhaled breath concentrations of benzene increased 2-fold for attack and search firefighters (p < 0.01) and 1.4-fold for outside vent firefighters (p = 0.02). Compared to interior attack, transitional attack resulted in 50% less uptake of pyrene (p = 0.09), 36% less uptake phenanthrene (p = 0.052), and 20% less uptake of fluorene (p < 0.01). Dermal absorption likely contributed to firefighters’ exposures in this study. Firefighters’ exposures will vary by job assignment and can be reduced by employing a transitional fire attack when feasible.

Atmospheric deposition and vegetable uptake of polycyclic aromatic hydrocarbons (PAHs) based on experimental and computational simulations

Experimental and computational simulations are conducted to assess the atmospheric gaseous deposition of polycyclic aromatic hydrocarbons (PAHs) and their uptake by four leafy vegetables (spinach, Chinese cabbage, Shanghai green cabbage, and romaine) during their growth in a greenhouse located in Shanghai. Sixteen individual PAHs on the US EPA priority list were measured in the aerials and roots of vegetables, air (both gas- and particle-phase), settled dust, and soil samples. Results showed that 2–3 ring PAHs were similarly dominant in the vegetable leaves, roots and airborne gas phase. However, 4–6 ring PAHs were dominant in the soils, dust, and airborne particle phase. Results also showed that the PAH concentrations in the vegetables were highest during the middle of the growth period. Both phenanthrene and anthracene in the vegetables had a significant positive correlation with chlorophyll-a and chlorophyll-b, indicating that the growth process influenced PAH concentrations in the vegetables. Furthermore, increasing dust-fall doses promoted PAH accumulation in Shanghai green cabbage and romaine, but inhibited PAH uptake in spinach and Chinese cabbage. Analyses using multivariate regressions and physical models found that gas-phase PAH absorption and soil absorption contributed to 90.6% and 9.4% of total PAH vegetable uptake, respectively. Although PAHs in the air were the dominant contributor to the total uptake, 13.2% of gas-phase PAHs resulted from soil volatilization. Atmospheric dust fall contributed to PAH uptake indirectly by increasing soil PAH concentrations. In addition, PAH uptake by vegetables via the air-shoot pathway displayed higher toxicity than the other pathways. This study provides a quantitative assessment of the pathways through which atmospheric PAHs lead to PAH contamination in a sample of commonly eaten leafy vegetables.

Urinary 1-hydroxypyrene and Skin Contamination in Firefighters Deployed to the Fort McMurray Fire.

BackgroundIn May 2016, firefighters from the province of Alberta, Canada deployed to a fire that engulfed the urban area of Fort McMurray. During the first days of the fire, firefighters experienced heavy smoke exposures during greatly extended work shifts. Urinary samples were collected post-deployment from three fire services for estimation of 1-hydroxypyrene (1-HP) concentration, reflecting exposure to polycyclic aromatic hydrocarbons (PAHs), to determine the effects of respiratory protective equipment (RPE) and skin hygiene in reducing internal doseMethodsUrine samples from one fire service (n = 62) were analyzed for 1-HP by two laboratories, using different assays (LC-MS/MS: GC-MS): remaining samples were analyzed just by LC-MS/MS. A Skin Exposure Mitigation Index (SEMI) was computed from questions on opportunities for changing clothing, showering, and washing during breaks. Regression analyses, using 1-HP ng/g creatinine as the dependent variable, assessed the effect of RPE and skin factors on PAH absorption, allowing for environmental exposure and potential confounders. Stratification identified key groups with equal delay in sample collection.Results1-HP was detected in 71.0% of 62 samples by LC-MS/MS and 98.4% by GC-MS, with good mutual agreement between the methods. In 171 post-fire samples, 1-HP corrected for creatinine was related to current cigarette smoking and recent barbeque. Among those with samples collected within 48 h, urinary 1-HP was correlated with estimated exposure(r = 0.53, P < 0.001). In those with only one rotation before urine sample collection, no effect was seen of RPE use but I-HP was significantly lower (P = 0.003) in those with those with a high score on the SEMI scale, indicating better access to factors mitigating skin absorption.ConclusionSkin exposure to PAHs is an important route of absorption in firefighters, which can be mitigated by good skin hygiene.

A realistic human skin model to study benzo[a]pyrene cutaneous absorption in order to determine the most relevant biomarker for carcinogenic exposure.

Polycyclic aromatic hydrocarbons (PAH) are ubiquitous pollutants, among which benzo[a]pyrene (B[a]P) is the only compound classified carcinogenic to humans. Besides pulmonary uptake, skin is the major route of PAH absorption during occupational exposure. Health risk due to PAH exposure is commonly assessed among workers using biomonitoring. A realistic human ex vivo skin model was developed to explore B[a]P diffusion and metabolism to determine the most relevant biomarker following dermal exposure. Three realistic doses (0.88, 8.85 and 22.11nmol/cm2) were topically applied for 8, 24, and 48h. B[a]P and its metabolites were quantified by liquid chromatography coupled with fluorimetric detection. The impact of time, applied dose, and donor age were estimated using a linear mixed-effects model. B[a]P vastly penetrated the skin within 8h. The major metabolites were 3-hydroxybenzo[a]pyrene (3-OHB[a]P) and 7,8,9,10-tetrahydroxy-7,8,9,10-tetrahydrobenzo[a]pyrene (B[a]P-tetrol). This latter predominantly derives from the most carcinogenic metabolite of B[a]P, benzo[a]pyrene-7,8-diol-9,10-epoxide (BPDE), as well as benzo[a]pyrene-9,10-diol-7,8-epoxide (reverse-BPDE). Benzo[a]pyrene-trans-7,8-dihydrodiol (B[a]P-7,8-diol) was a minor metabolite, and benzo[a]pyrene-trans-4,5-dihydrodiol (B[a]P-4,5-diol) was never quantified. Unmetabolized B[a]P bioavailability was limited following dermal exposure since less than 3% of the applied dose could be measured in the culture medium. B[a]P was continuously absorbed and metabolized by human skin over 48h. B[a]P-tetrol production became saturated as the applied dose increased, while no effect was measured on the other metabolic pathways. Age had a slight positive effect on B[a]P absorption and metabolism. This work supports the relevance of B[a]P-tetrol to assess occupational exposure and carcinogenic risk after cutaneous absorption of B[a]P.

Correction to Importance of Dermal Absorption of Polycyclic Aromatic Hydrocarbons Derived from Barbecue Fumes.

Correction to Importance of Dermal Absorption of Polycyclic Aromatic Hydrocarbons Derived from Barbecue Fumes.

Measurements of Pressure Effects on PAH Distribution and 2D Soot Volume Fraction Diagnostics in a Laminar Non-premixed Coflow Flame

The soot formation process has been investigated at pressures up to 16 bar using a non-premixed laminar coflow flame with nitrogen-diluted ethylene. 2D diffuse line-of-sight attenuation (2D LOSA) and planar laser-induced incandescence (PLII) were used to measure soot volume fraction (SVF). The peak SVF increased exponentially with increasing pressure, and the spatial distribution of soot volume fraction changed substantially. At pressures below 6 bar, the two techniques agreed well. At pressures above 6 bar, the techniques began to disagree, with 2D LOSA showing higher peak SVF values at a location lower in the wings of the flame compared to PLII. Errors in the LOSA measurements due to the molecular absorption of PAHs were assessed by performing measurements with bandpass filters centered at 435 nm and at 647 nm. Furthermore, the evolution of polycyclic aromatic hydrocarbons (PAH) in the flame was studied using planar laser-induced fluorescence (PLIF) with the excitation laser set at 282.85 nm and compare...

Potential sources and meteorological factors affecting PM2.5-bound polycyclic aromatic hydrocarbon levels in six main cities of northeastern Italy: an assessment of the related carcinogenic and mutagenic risks.

A yearlong sampling campaign (2012-2013) was conducted in six major cities of the Veneto region to investigate the spatial-temporal trends and the factors affecting the polycyclic aromatic hydrocarbon (PAHs) variations and identify the local sources. Sixty samples per city were collected for analyses in every alternate month (April, June, August, October, December, and February): 10 samples per sampling site in 10 consecutive days of the months selected. Samples were ultrasonically extracted with acetonitrile and processed through high-performance liquid chromatography. Total Σ-PAH concentrations ranged from 0.19 to 70.4ngm-3 with a mean concentration of 11.5ngm-3. The mean benzo[a]pyrene (BaP) concentration reached 2.0ngm-3, which is two-times higher than the limit set by the European Union. BaP contributed for 17.4% to the total concentration of PAHs, which showed the same pattern across the region with maxima during cold months and minima in the warm period. In this study, PAHs showed an inverse relationship with temperature, solar radiation, wind speed, and ozone. According to this study, biomass burning for household heating and cooking, followed by gaseous PAHs absorption on particles due to low atmospheric temperature, were the main reasons for increasing PAHs concentration in winter. Health risk, evaluated as lifetime lung cancer risk (LCR), showed a potential carcinogenic risk from the airborne BaPTEQ six-fold higher in the cold season than in the warm one. Diagnostic ratios and conditional probability functions were used to locate the sources, and results confirmed that local emission, overall domestic heating, and road transport exhausts were responsible for higher concentration rates of PAHs as well as of PM2.5.

Visible-Light-Induced Photocatalytic Degradation of PAH-Contaminated Soil and Their Pathways by Fe-Doped TiO2 Nanocatalyst

The aim of the present study was to establish the photocatalytic efficiency of Fe-doped TiO2 nanocatalysts toward polycyclic aromatic hydrocarbons (PAHs), which were phenanthrene, anthracene, and fluoranthene, contaminated soil under visible irradiation. The morphology, phase, and particle size of the prepared nanocatalyst have been studied as a first mention in literature. The photoresponse of the TiO2 extends from UV region to the visible region was proved by the diffuse reflectance spectrophotometry (DRS). The surface area is greatly increased though the Fe-doped TiO2 compared with the bare TiO2. The pH value of the media showed the beneficial to PAH absorption on the Fe-doped TiO2 under the alkaline condition due to the surface catalyst possesses much negative charge, which is increase in percentage of PAH degradation. Based on GC-MS study, the mechanism of photoactivity of the selected PAHs involves hydroxylation, ring opening, and rearrangement reactions. The main intermediates of PAH photodegradation were found to be 9-octadecanoic acid, heptadecane, octadecane, cyclohexane (1-hexadecylheptadecyl), and 15-hydroxypentadecanoic acid.

Importance of Dermal Absorption of Polycyclic Aromatic Hydrocarbons Derived from Barbecue Fumes

Despite the ubiquity and carcinogenicity of polycyclic aromatic hydrocarbons (PAHs), their dermal absorption for the general population has not been adequately addressed. Aiming to verify the importance of dermal absorption of PAHs, barbecue (BBQ) in Guangzhou, China was chosen as a case study. Urine samples were collected and analyzed for nine hydroxyl (OH)-PAHs. Air, food, and cotton clothing samples were analyzed for 16 PAHs. Dietary exposure was the dominant exposure route with the greatest amounts of OH-PAH excretion and PAH intake. Dermal intake of low molecular-weight PAHs was greater than inhalation intake from the occurrence of atmospheric PAHs. In addition, the net excreted amounts of OH-naphthalene, OH-fluorene, OH-phenanthrene, and OH-pyrene via dermal absorption were 367, 63, 98, and 28 ng, respectively, upon 2.5-h exposure, comparable to those via combined dermal and inhalation exposure, which were 453, 98, 126, and 38 ng. The ratios of excretion to intake via dermal absorption were 0.11, 0.036, and 0.043 for fluorene, phenanthrene, and pyrene, respectively, lower than the ratios from dietary exposure (0.38, 0.14, and 0.060) but higher than the ratios from inhalation (0.097, 0.016, and 0.025). In the case of BBQ fumes, dermal absorption was a more important pathway for intake of low molecular-weight PAHs than inhalation.

Absorption of polycyclic aromatic hydrocarbons by a highly absorptive polymeric medium

The efficacy of a lightly cross-linked polymeric bead to absorb polycyclic aromatic hydrocarbons (PAHs) from the surface of fresh- and salt-water in a simulated oil-spill scenario was assessed in this study. A layer of PAHs at the water surface was created by first preparing the PAHs in hexane and then carefully spiking this mixture onto the surface of water. Beads were then applied to the surface of the organic phase and the amount of hydrocarbons absorbed by the beads was examined at prescribed time intervals and at different temperatures. Absorption of PAHs into the beads was exhaustive with ∼86 ± 4% being selectively removed from the organic phase by 120 s. First order reaction rates best described the uptake kinetics and absorption rates ranged from 0.0085 (naphthalene) to 0.0325 sˉ1 (dibenzo[a,h]anthracene). Absorption of PAHs into the beads was driven by molecular volume (A3). Uptake rates increased markedly for PAHs with molecular volumes between 130 A3 and 190 A3. Beyond this molecular volume there was no apparent change in the rate of uptake. This study shows that these polymeric beads have a high affinity for PAHs and can be used under various environmental conditions with negligible difference in absorptive efficacy.

Degradation of toxic PAHs in water and soil using potassium zinc hexacyanoferrate nanocubes

Polycyclic aromatic hydrocarbons (PAHs) the ubiquitous, persistent and carcinogenic environmental contaminants have raised concern worldwide. Recently, their removal methodologies are advanced after exploring nanomaterials. Therefore, degradation of selected toxic PAHs (3–5 rings) using potassium zinc hexacyanoferrate (KZnHCF) nanocubes was studied. Highly crystalline and sharp KZnHCF nanocubes (∼100 nm) were obtained by green route using sapindus mukorossi. In both water and soil, anthracene and phenanthrene were degraded to maximum extent (80–93%), whereas, the degradation of fluorene, chrysene and benzo (a) pyrene were ∼70–80%.Because of small size (lower molecular weight), large number of anthracene and phenanthrene molecules were adsorbed on catalyst as compared to other PAHs. Higher degradation of PAHs in water than in the soil is attributed to the easy absorption of PAHs on catalyst in water and slow diffusion of PAHs on organic content of soil. PAHs were degraded at the concentration of 50 mg/L, 25 mg catalyst dose, neutral pH and solar irradiation. Higher proficiency of the catalyst was revealed by degradation of PAHs into small and non-toxic by-products such as malealdehyde, 4-oxobut-2-enoic acid and o-xylene. Overall, the potential KZnHCF nanostructures open future scope for eradication of other pollutants from the environment.

The evolution of pollution profile and health risk assessment for three groups SVOCs pollutants along with Beijiang River, China.

Three important groups of semi-volatile organic compounds (SVOCs), polycyclic aromatic hydrocarbons (PAHs), organic chlorinated pesticides (OCPs) and phthalate esters (PAEs), were produced by various human activities and entered the water body. In this study, the pollution profiles of three species including 16 PAHs, 20 OCPs and 15 PAEs in water along the Beijiang River, China were investigated. The concentrations of Σ16PAHs in the dissolved and particulate phases were obtained as 69-1.5×102 ng L-1 and 2.3×103-8.6×104 ngg-1, respectively. The levels of Σ20OCPs were 23-66ng L-1 (dissolved phase) and 19-1.7×103 ngg-1 (particulate phase). Nevertheless, higher levels of PAEs were found both in the dissolved and particulate phases due to abuse use of plastic products. Furthermore, non-cancer and cancer risks caused by these SVOCs through the ingestion absorption and dermal absorption were also assessed. There was no non-cancer risk existed through two kinds of exposure of them at current levels, whereas certain cancer risk existed through dermal absorption of PAHs in the particulate phase in some sampling sites. The results will show scientific insights into the evaluation of the status of combined pollution in river basins, and the determination of strategies for incident control and pollutant remediation.