Group Of Polycyclic Aromatic Hydrocarbons Research Articles

Eco-Friendly Inorganic Binders: A Key Alternative for Reducing Harmful Emissions in Molding and Core-Making Technologies

Many years of foundry practice and much more accurate analytical methods have shown that sands with organic binders, in addition to their many technological advantages, pose risks associated with the emission of many compounds, including harmful ones (e.g., formaldehyde, phenol, benzene, polycyclic aromatic hydrocarbons, and sulfur), arising during the pouring of liquid casting alloys into molds, their cooling, and knock-out. The aim of this research is to demonstrate the potential benefits of adopting inorganic binders in European iron foundries. This will improve the environmental and working conditions by introducing cleaner and more ecological production methods, while also ranking the tested binders studied in terms of their harmful content. The article pays special attention to the analysis of seven innovative inorganic binders and one organic binder, acting as a reference for emissions of gases from the BTEX (benzene, toluene, ethylbenzene, and xylenes) and PAHs (polycyclic aromatic hydrocarbons) groups and other compounds such as phenol, formaldehyde, and isocyanates (MDI and TDI) generated during the mold pouring process with liquid metals. The knowledge gained will, for the first time, enrich the database needed to update the Reference Document on The Best Available Techniques for the Smitheries and Foundries Industry (SF BREF).

Assessment of parent and alkyl -PAHs in surface sediments of Iranian mangroves on the northern coast of the Persian Gulf: Spatial accumulation distribution, influence factors, and ecotoxicological risks

Spatial patterns, potential origins, and ecotoxicological risk of alkylated (APAH) –and parent –(PPAH) polycyclic aromatic hydrocarbons (PAHs) were studied in mangrove surface sediments along the northern coasts of the Persian Gulf, Iran. The mean total concentrations (ngg−1dw) ∑32PAH, ∑PPAHs and ∑APAHs in sediments were 3482 (1689–61228), 2642 (1109–4849), and 840 (478–1273), respectively. The spatial variability was similar among these PAH groups, with the highest levels occurring in Nayband National Marine Park (NNMP). Physicochemical environmental factors, such as sediment grain size, and total organic carbon (TOC) contents, are significant factors of PAH distribution. These findings suggest that PAH pollution level is moderate-to-high, supporting the current view that mangrove ecosystems are under intensive anthropogenic impacts, such as petrochemical, oil and gas loads, port activities, and urbanization. Non-parametric multidimensional scaling (NPMDS) ordination demonstrated that NNMP mangrove is the critical site exhibiting high loading of PAH pollutants. Here, for the first time in this region, Soil quality guidelines (SQGs), Toxic equivalency quotient (TEQ), Mutagenic equivalency quotient (MEQ), and composition indices comprising Mean maximum permissible concentration quotient (m-MPC-Q), and Mean effect range median quotient (m-ERM-Q) methods were used to have a comprehensive risk assessment for PAH compounds and confirmed medium-to-high ecological risks of PAHs in the study area, particularly in the western part of the Gulf, highlighting the industrial impacts on the environment.

Sorption Processes of Selected PAHs on Selected Fire-Resistant Materials Used in Special Firefighter Clothing.

Fires constitute a significant threat due to the pollutants emitted and the destruction they cause. People who take part in firefighting operations must be equipped with appropriate tools, including special clothing that will allow them to work and guarantee safety. One of the threats is represented by compounds from the PAH (Polycyclic Aromatic Hydrocarbons) group, which are characterized by high toxicity and carcinogenicity. Therefore, it is important that the materials used constitute a barrier to contamination. Various materials from which individual elements of special firefighter's clothing are made were tested. Additionally, the effect of height on the possibility of sorption of PAH compounds on a given type of material was analyzed. Based on the obtained analysis results, it was found that both the type of material and the zone in which the clothing items are used are important in the sorption processes of pollutants. For example, PAHs with high molecular weight are most likely to settle on rubber, i.e., the material from which shoes are made, with the exception of Chrysene, whose presence was found primarily in aramid fibers, i.e., the material from which trousers and jackets are made. However, among PAHs with low molecular weight, compounds such as Methylnaphthalene,1- and Fluorene were sorbed on the rubber surface in large quantities. The only compound that is present in comparable amounts in all materials is Acenaphthylene. Data in this area may be important for taking further actions related to the modification of materials used in special fire brigade clothing and in their cleaning processes.

Benzo(a)Pyrene in PM10 - Air Monitoring Results in Poland

Abstract Benzo(a)pyrene (B(a)P) is an extremely toxic substance from the group of PAHs (polycyclic aromatic hydrocarbons). These compounds are formed mainly during combustion processes, and they are transported on the surfaces of suspended aerosol in the air. In Poland, both the concentration of suspended dusts and the amount of B(a)P are among the highest in Europe. The aim of the research was to compare levels of B(a)P concentrations in various locations in Poland. Based on multi-year data, coming from the period 2009-2019, linear trends in changes of these levels were determined with the least squares method. The annual courses of B(a)P concentrations in the air show clear seasonal variations. The highest concentrations are observed in the autumn-winter months, the lowest in the spring-summer months. The annual courses of B(a)P/PM10 ratio show clear seasonal variations. This ratio allows to evaluate the content of B(a)P in PM10 particles, expressed in ngB(a)P/μgPM10. The highest ratio values are observed in the autumn-winter months, the lowest ones in the spring-summer months. At most air monitoring stations, the assigned B(a)P concentration trend lines show a weak decline.

Benzo(a)pyrene - an air pollutant harmful to health in European countries

Background: Benzo(a)pyrenes are organic compounds from the polycyclic aromatic hydrocarbons group known for their carcinogenic properties. Benzo(a)pyrenes are formed as a result of incomplete combustion of organic matter, such as biomass or fossil fuel.Aim of the study: To investigate whether respiratory diseases and malignant neoplasm-related deaths correlate to air concentrations of benzo(a)pyrene in European countries.Material and methods: Publicly available data were obtained regarding benzo(a)pyrene concentration from the EUROSTAT database, as well as territorial division in accordance with NUTS 2. Diseases were defined according to ICD-10.Results: There is a positive correlation of medium effect (r = 0.442; p < 0.001) between the annual average concentration of benzo(a)pyrene and deaths due to malignant neoplasms, with the strongest correlation being malignant bladder neoplasms (r = 0.502; p < 0.001). There is a positive correlation of a moderately weak effect (r = 0.221; p = 0.002) between the annual average concentration of benzo(a)pyrene and deaths due to respiratory diseases, with the strongest correlation for pneumonia of various etiologies, which is a positive correlation of a medium effect (r = 0.496; p < 0.001). Linear regression models showed that reducing the concentration of benzo(a)pyrene by 1 ng/m3 will reduce the frequency of deaths due to malignant laryngeal neoplasms by 0.816 per 1000 residents, malignant bladder neoplasms by 1.41 per 1000 residents, and deaths due to pneumonia by 11.26 per 1000 residents.Conclusions: We have found that benzo(a)pyrene concentration has a moderate correlation with death due to respiratory diseases and malignant neoplasms. More in-depth studies regarding other factors, e.g. the age of the patient are needed.

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.

Preferential association of polycyclic aromatic hydrocarbons (PAHs) with soil colloids at an e-waste recycling site: Implications for risk of PAH migration to subsurface environment

Polycyclic aromatic hydrocarbon (PAH) contamination at e-waste recycling sites poses high ecological and human-health risks. Of note, PAHs in surface soils can be mobilized through colloid-facilitated transport, and may migrate into the subsurface and pollute groundwater. Here, we show that the colloids released from the soil samples at an e-waste recycling site in Tianjin, China contain high concentrations of PAHs, with total concentrations of 16 PAHs as high as 1520 ng/g dw. Preferential association of the PAHs with the colloids is observed, with the distribution coefficients of PAHs between colloids and bulk soil often above 10. Source diagnostic ratios show that soot-like particles are the main source of PAHs at the site, due to the incomplete combustion of fossil fuels, biomass, and electronic wastes during the e-waste dismantling practices. Due to their small sizes, a large fraction of these soot-like particles can be remobilized as colloids, and this explains the preferential association of PAHs with colloids. Moreover, the colloids-soil distribution coefficients are higher for the low-molecular-weight PAHs than for the high-molecular-weight ones, possibly attributable to the different binding routes/modes of these two groups of PAHs to the particles during combustion. Notably, the preferential association of PAHs with colloids is even more pronounced for the subsurface soils, corroborating that the presence of PAHs in the deeper soils is primarily the results of downward migration of PAH-bearing colloids. The findings highlight the important role of colloids as a vector for the subsurface transport of PAHs at e-waste recycling sites, and call for further understanding of colloid-facilitated transport of PAHs at e-waste recycling sites.

Effect of Hybrid Filler, Carbon Black-Lignocellulose, on Fire Hazard Reduction, including PAHs and PCDDs/Fs of Natural Rubber Composites.

The smoke emitted during thermal decomposition of elastomeric composites contains a significant number of carcinogenic and mutagenic compounds from the group of polycyclic aromatic hydrocarbons, PAHs, as well as polychlorinated dibenzo-p-dioxins and furans, PCDDs/Fs. By replacing carbon black with a specific amount of lignocellulose filler, we noticeably reduced the fire hazard caused by elastomeric composites. The lignocellulose filler reduced the parameters associated with the flammability of the tested composites, decreased the smoke emission, and limited the toxicity of gaseous decomposition products expressed as a toximetric indicator and the sum of PAHs and PCDDs/Fs. The natural filler also reduced emission of gases that constitute the basis for determination of the value of the toximetric indicator WLC50SM. The flammability and optical density of the smoke were determined in accordance with the applicable European standards, with the use of a cone calorimeter and a chamber for smoke optical density tests. PCDD/F and PAH were determined using the GCMS-MS technique. The toximetric indicator was determined using the FB-FTIR method (fluidised bed reactor and the infrared spectrum analysis).

Assessment of environmental risk related to the polycyclic aromatic hydrocarbons (PAH) in the sediments along the eastern Adriatic coast

Polycyclic aromatic hydrocarbons (PAH) were investigated in the sediments at 24 locations in the coastal area of Adriatic Sea. Total PAH concentrations ranged from 14,98 to 26145,62 µg kg-1, with the highest levels determined in the sediments of Šibenik Bay and the lowest in the sediment near Island of Pag. Unsubstituted PAH were prevailing PAH group in the sediments from the Šibenik Bay and in the Coastal area, while methyl-substituted PAH were dominant group in the sediments of the Kaštela Bay. In order to estimate the possible toxicological significance of PAH concentrations, Sediment Quality Assessment was done according to three different sets of sediment quality guidelines. A high environmental risk was calculated for each station in Šibenik Bay; for the station in vicinity of the Industrial port of Split and for the two stations in Coastal zone. Low environmental risk was determined in less urbanised areas such as Island of Pag. Sediment extracts were further analysed for acute toxicity by measurements of decrease in bioluminescence upon exposure to sediment extracts. Obtained results show disagreement between sediment toxicity predicted upon PAH levels in sediment and experimentally obtained sediment toxicity. Sediment extracts in which low PAH levels were measured showed high acute toxicity indicating that concentrations of PAH alone are a poor indicator of sediment toxicity. Correlation analysis between concentrations of specific PAH compounds and toxicity revealed the strongest association between acute sediment toxicity and sulphur-containing PAH suggesting the S-PAH should be considered in sediment toxicity assessment.

Biotransformation as a tool for remediation of polycyclic aromatic hydrocarbons from polluted environment - review on toxicity and treatment technologies

Polycyclic aromatic hydrocarbons, a prominent family of persistent organic molecules produced by both anthropogenic and natural processes, are widespread in terrestrial and aquatic environments owing to their hydrophobicity, electrochemical stability and low aqueous solubility. Phenanthrene and naphthalene belong to the group of polycyclic aromatic hydrocarbons whose occurrence are reported to be relatively higher. The bioremediation mode of removing the toxicities of these two compounds has been reported to be promising than other methods. Most of the microbial classes of bacterial, fungal and algal origin are reported to degrade the target pollutants into non-toxic compounds effectively. The review aims to give an overview on toxicological studies, identification and enrichment techniques of phenanthrene and naphthalene degrading microbes and the bioremediation technologies (microbial assisted reactors, microbial fuel cells and microbial assisted constructed wetlands) reported by various researchers. All the three modes of bioremediation techniques were proved to be promising on different perspectives. In the treatment of phenanthrene, a maximum recovery of 96% and 98% was achieved in an aerobic membrane reactor with Bacillus species and single chamber air cathode microbial fuel cell with Acidovorax and Aquamicrobium respectively were reported. With the constructed wetland configuration, 95.5% of removal was attained with manganese oxide based microbial constructed wetland. The maximum degradation efficiency reported for naphthalene are 99% in a reverse membrane bioreactor, 98.5% in a marine sediment microbial fuel cell and 92.8% with a low-cost sandy soil constructed wetland.

Identification and classification of PAH in asphalt binders with FTIR spectroscopy and multivariate analysis methods

Reclaimed asphalt pavements (RAP) with increased contents of polycyclic aromatic hydrocarbons (PAH) are restricted for reuse due to their harmful effects on humans and the environment. This work investigated whether Fourier transform infrared (FTIR) spectroscopy is suitable for a fast and simple identification and quantification of PAH in binders recovered from reclaimed asphalts. For this, the binders from 34 RAP samples were recovered using a rapid procedure developed at the Universität Kassel and were examined with infrared spectroscopy. The obtained spectra were pre-processed (Standard Normal Variate transformation, 1st derivative) and evaluated using a combination of factor analysis and linear discriminant analysis. The results showed that various PAH groups with differently pronounced aromatic structures are present in the binders. However, with FTIR spectroscopy combined with the multivariate methods, a statistical model was developed allowing for the differentiation between the PAH groups and also for the distinction between PAH contents below or above the threshold of 25mg/kg valid in Germany.

Methodical approaches to the detection polycyclic aromatic hydrocarbons in ambient air (analytical review)

Among the persistent organic pollutants of atmospheric air, a special place is occupied by a group of polycyclic aromatic hydrocarbons (PAHs) or polyarenes due to their high carcinogenic hazard. In view of the ubiquitous presence of these substances in the atmospheric air, low values of hygienic standards and values of reference concentrations (RfC) for chronic inhalation exposure, the qualitative and quantitative identification of PAHs is the critical task. Purpose is to analyze modern methodological approaches used in laboratory practice to determine polyarenes in atmospheric air on the base of Russian and foreign sources. The paper considers modern methods for the analytical control of PAHs in atmospheric air, officially approved in the Russian Federation and presented in the world literature. The search for literary sources was carried out using the PubMed, RSC Publishing, Springer Nature, SCOPUS, eLIBRARY.RU databases. An analysis of the methodological and scientific and technical literature on methods for the determination of PAHs in atmospheric air made it possible to identify the main directions of methodological developments used in modern laboratory practice for the analytical control of polyarenes in air. The advantages and disadvantages of specific methods, individual stages of analysis, conditions for sampling, storage and transportation of samples, which together can lead to false positive or false negative results, are presented. Conclusion. Modern methods for the analysis of polyarenes in atmospheric air are the result of continuous improvement in the technique of performing individual analytical procedures, the development of new methodological approaches to solving analytical problems, the emergence of new, more advanced measuring and auxiliary equipment, which makes it possible to develop highly sensitive and highly selective methods for measuring toxicants in the human environment at the level of MPCdaily average, MPCone-time and RfC for chronic inhalation exposure.

Phthalate acid esters and polycyclic aromatic hydrocarbons concentrations with their determining factors among Chinese pregnant women: A focus on dietary patterns

BackgroundPregnant women are susceptible to adverse health effects associated with phthalate acid esters (PAEs) and polycyclic aromatic hydrocarbons (PAHs), and diet is a significant exposure source. Little is known about the contributions of dietary patterns during pregnancy to the exposure variability of these environmental contaminants. ObjectivesTo identify dietary patterns in relation to PAEs and PAHs exposure in the Chinese pregnant population. MethodsDietary data and urinary concentrations of environmental pollutants were obtained from 1190 pregnant women in the Tongji Birth Cohort (TJBC). PAEs and PAHs were measured in spot urine samples. Food intake was assessed using a food-frequency questionnaire. Dietary patterns were constructed by principal component analysis (PCA). Through PCA, we also extracted three chemical mixture scores that represent different co-exposure patterns of PAEs and PAHs. Multiple linear regression models were adopted to identify predictors of PAEs and PAHs exposure. ResultsFour dietary patterns were identified by PCA that explained 44.9 % of the total variance of food intake. We found egg-dairy products pattern, whole grain-tuber crop pattern, and meat-aquatic products pattern were positively associated with specific pollutants exposure. In contrast, fruit-nut-vegetable pattern was negatively correlated with PAEs and PAHs exposure. Every SD increase in this pattern score was associated with 14.36 % reduced mono(2-ethyl-5-oxohexyl) phthalate (MEOHP) (95 % CI: −24.50 ~ −2.96, p-trend = 0.01), 10.86 % reduced 2-hydroxynaphthalene (2-OHNap) (95 % CI: −20.07 ~ −0.60, p-trend = 0.04), 19.35 % reduced 9-hydroxyphenanthrene (9-OHPhe) (95 % CI: −34.49 ~ −0.70, p-trend = 0.01), and 8.33 % reduced scores of PAHs group (95 % CI: −15.97 ~ −0.10, p-trend = 0.02). In addition, disposable tableware usage and passive smoking were suggested as potentially modifiable sources of PAEs and PAHs exposure, respectively. ConclusionAdhering to egg-dairy products pattern, whole grain-tuber crop pattern, and meat-aquatic products pattern may be related to increased PAEs and PAHs exposure, while following fruit-nut-vegetable pattern seems to correlate with a lower burden of such exposure.

Phenanthrene uptake and translocation by Panicum miliaceum L. tissues: an experimental study in an artificial environment.

Polycyclic aromatic hydrocarbons (PAHs), as priority organic pollutants, are capable of accumulation in plants. Phenanthrene (Phe) is one of the most abundant low-molecular-weight PAH in the environment which is commonly used as a model PAH in many phytoremediation studies and as a representative compound for all PAHs group. This paper highlights the uptake, translocation, and accumulation of Phe by growing proso millet (Panicum miliaceum L.) in a pot experiment, subjected to 500, 1000, 1500, and 2000ppm of Phe treatment after 15 and 30days. Phe naturally existed in P. miliaceum and its concentration showed a time-dependent reduction in treated plant tissues as well as in perlites. Phe concentration in shoots was higher than in roots. During the aging process, the uptake of Phe was diminished whereas translocation factor (TF) demonstrated an overall increasing trend among treatments. The shoot concentration factor (SCF) values were higher than those of root concentration factor (RCF) on both days 15 and 30 and the highest values for both parameters were achieved in 500ppm of Phe. Both RCFs and SCFs generally tended to decrease with the increase of perlite Phe concentrations. These results suggested that Phe tended to transfer to the shoots and be metabolized there. The Phe concentration revealed a significant decline in all levels of treatment on both 15 (84 to 96%) and 30 (76 to 94%) days. Therefore, the presence of P. miliaceum was effective in promoting the phytoremediation of Phe polluted perlites.

Using the results of environmental monitoring for economic calculations on the example of adjusting the cost of land plots using the indicative method

The purpose of the work is to compare the ranges of the cadastral value of land plots with the environmental situation in these territories. The issue is considered on the example of the impact of polycyclic aromatic hydrocarbons (PAH) on industrial-urbanized territories adjacent to two enterprises, one of which is located in Moscow (a waste incineration plant), the other in the Moscow region (a plant producing metal products, Podolsk). The assessment of the toxic impact of biologically available PAHs on these territories was carried out using a new indicative method developed by the author. A feature of this method is taking into account not only the concentration of pollutants in the objects under study, but also the physicochemical and toxicological properties of each compound. The results of the study, presented in cartographic form, were compared for the first time with maps of the cadastral value of land plots located in the studied territories. The comparison showed that the price of land plots in most cases is not proportional to the level of toxic effects of polyaromatic hydrocarbons, that is, the environmental component was not taken into account when forming their cost. However, the obvious connection between chemical pollution of territories and economic damage (including damage to the health of the population living in polluted territories) gives reason to propose a way to correct the cadastral value by dividing it by a correction factor that reflects the degree of contamination of the territory with compounds of the PAH group and represents the equivalent of the concentration of one of the most toxic polycyclic aromatic hydrocarbons, benzo(a)pyrene, the impact of which on humans and the environment corresponds to a similar total impact of PAHs contained in the soil of a particular territory.

Simultaneous Determination of Multi-Class Pesticide Residues and PAHs in Plant Material and Soil Samples Using the Optimized QuEChERS Method and Tandem Mass Spectrometry Analysis.

New analytical approaches to the simultaneous identification and quantification of 94 pesticides and 13 polycyclic aromatic hydrocarbons (PAHs) in five representative matrices (pepper, apple, lettuce, wheat, and soil) were developed. The analyses were based on gas chromatography coupled with triple quadrupole tandem mass spectrometry (GC-MS/MS). The procedure was optimized by changing the solvent used during the extraction, from acetonitrile to the acetone: n-hexane mixture at a volume ratio of 1:4 (v/v), as well as the use of a reduced amount of water during the extraction of compounds from cereals. An additional modification was the use of florisil instead of GCB in the sample cleanup step. A full method validation study was performed, at two concentration levels (LOQ and 1000 × LOQ), which showed satisfactory results for all analytes from the PAHs group, with recoveries ranging from 70.7–115.1%, and an average RSD of 3.9%. Linearity was tested in the range of 0.001–1.000 mg/kg and showed coefficients of determination (R2) ≥ 0.99 for all PAHs. Satisfactory recovery and precision parameters (LOQ and 100 × LOQ) were achieved for almost all analytes from the pesticide group in the range of 70.1–119.3% with the mean RSD equal to 5.9%. The observed linearity for all analytes in the concentration range of 0.005–1.44 mg/kg was R2 ≥ 0.99, with the exception of famoxadone, chizalofop-p-ethyl, prothioconazole, spirodiclofen, tefluthrin, and zoxamid. The extended uncertainties were estimated, using a top-down approach of 9.9% (average) and 15.3% (average) for PAHs and pesticides samples, respectively (the coverage factor k = 2, the 95% confidence level). Ultimately, the method was successfully applied to determine pesticide residues in commercial samples of fruit, vegetables and grain, and soil samples for PAHs, which were collected from selected places in the Podkarpacie region. A total of 38 real samples were tested, in which 10 pesticides and 13 PAHs were determined. Proposed changes allow us to shorten the sample preparation time (by 20%) and to reduce the consumption of organic solvents (by 17%). The use of florisil for sample cleanup, instead of GCB, improves the recovery of compounds with flat particles.

The Potential of Oxygenates to Increase the Risk of Exposure to Polycyclic Aromatic Hydrocarbons through Groundwater Contamination

The Clean Air Act (42 U.S. Code § 7401) is one of the United States of America’s most influential environmental laws. Under the Clean Air Act Amendments of 1990, oxygen-containing organic compounds must be added to some fossil fuels with the goal of combating CO2 and particulate emissions. However, one major implication is the effect of co-solvency on the leaching potentials of polycyclic aromatic hydrocarbons (PAHs) into groundwater. Our research investigated this effect on three groups of recalcitrant PAHs that are present in diesel fuel. Our results reveal that ethanol addition enhances the leaching potentials of these otherwise hydrophobic contaminants, with 10% ethanol (E10) resulting in elution of all the PAHs studied. While 5% ethanol addition to diesel fuel resulted in the elution of an average of 2.5% of all the trimethylnaphthalenes and 6.0% of the C2 alkylphenanthrenes present in diesel fuel, 10% ethanol addition led to the elution of more than 80% of each of the studied trimethylnaphthalene peaks and more than 70% of each of the studied C2 alkylphenanthrene peaks present in diesel fuel. In view of the known mutagenic and carcinogenic risks associated with exposure to PAHs through groundwater contamination, our study highlights the need for energy scientists to carefully consider the environmental and health implications of ethanol-blended innovations holistically. It is not enough to save the atmosphere but ruin the hydrosphere and most importantly, human health.

Analysis of Polycyclic Aromatic Hydrocarbon Content in Ash from Solid Fuel Combustion in Low-Power Boilers

The production of thermal energy is one of the sources of environmental pollution, especially when it uses traditional fossil fuels (in particular hard and brown coal). Burning conventional fuels contributes to air pollution because of emitting gases and producing waste after the process of burning in the form of ash. The work below was aimed at determining the indirect emission of PAHs in the form of fly ash, depending on the type of fuel burned. The conducted research showed which solid fuel combustion content leaves the lowest content of PAH in the fly ash. This work contains the analysis and assessment of the content of 16 PAHs (polycyclic aromatic hydrocarbons) in fly ash from the combustion of five selected solid fuels in low-power boilers. The following fuels were chosen for the research: hard coal with granulation above 60 mm, coal with the grain size of 25–80 mm, coal with the grain size of 8–25 mm, pellets with the grain size of 6 mm, and mixed dry wood. The results of the research showed that the most frequent and most concentrated compounds were naphthalene and acenaphthylene from the PAH group. These hydrocarbons have the smallest number of rings in a molecule. It was also found that the content of the LMW (Low Molecular Weight Polycyclic Aromatic Hydrocarbons) fractions in the fly ash from the analyzed fuels in ∑PAHs exceeds 57% in the case of 6 mm pellets and in the case of the ash from wood and hard coal when the grain size >60 mm. The opposite dependence can be observed in the case of the HMW (High Molecular Weight Polycyclic Aromatic Hydrocarbons) fraction.

Occurrence of polycyclic aromatic hydrocarbons in human diet - exposure and risk assessment to consumer health.

Polycyclic aromatic hydrocarbons (PAHs) are environmental pollutants, they are also present in food, in which their presence results from environmental pollution and food processing processes. Many compounds from this group, such as benzo(a)pyrene show important toxicity, including genotoxic carcinogenicity. In food heavier PAHs significantly toxic are observed. The aim of the study was assessment of consumers exposure to PAHs from the diet of surveyed respondents. The assessment of contaminants content in daily food rations is characterized by less uncertainty factor than the assessment based on data on the contamination of individual foodstuffs and their consumption by humans. Research material consisted of daily diets obtained from respondents participating in the study. Content of 22 PAHs (fluorene, phenanthrene, anthracene, fluoranthene, pyrene, benzo(c)fluorene, benz(a)anthracene, chrysene, 5-methylchrysene, perylene, benzo(b)fluoranthene, benzo(k)fluoranthene, benzo(j)fluoranthene, benzo(e) pyrene, benzo(a)pyrene, benzo(ghi)perylene, indeno(1,2,3-cd)pyrene, dibenzo(a,h)anthracene, dibenzo(a,e)pyrene, dibenzo(a,l)pyrene, dibenzo(a,h)pyrene, dibenzo(a,i)pyrene) in each of diets was tested using liquid chromatography with a fluorescence detector. The samples were purified by saponification, size exclusion chromatography (SEC) and solid phase extraction (SPE). 52 respondents (n=52) took part in the study. The highest median of PAHs were found for pyrene (1.412 μg/kg), phenantrene (1.276 μg/kg), fluorene (1.151 μg/kg) and fluoranthene (1.087 μg/kg), they were about 10-80 higher than the levels of heavier PAHs. In group of heavy PAHs quantitatively prevailed benzo(e)pyrene (0.109 μg/kg), benzo(b) fluroanthene (0.070 μg/kg), benzo(ghi)perylene (0.065 μg/kg) and perylene (0.059 μg/kg). Generally the median level of contamination with light PAHs was 6.045 μg/kg, while with heavy ones 0.504 μg/kg, in the case of the sum of 4 PAHs regulated in EU law content was 0.301 μg/kg. In the tested samples average 24% of the PAH content was pyrene, light PAHs with a lower toxicity potential accounted for 92% of the content of tested compounds. Sum of 4 regulated PAHs accounted for 58% of content compounds selected by the EU as significant for the assessment of food contamination by PAHs. The composition of the participants' diets was analyzed in terms of determining factors influencing on high levels of PAHs. They were high fat level and presence of smoked or grilled meat and fish products. The mean exposure to benzo(a)pyrene was 0.52 ng/kg b.w. per day, while for the sum of 4 PAHs 3.29 ng/ kg b.w. per day. For light PAHs high exposure was 90.6 ng/kg b.w. per day, while for heavy PAH it was 10.7 ng/kg b.w. per day. Risk assessment was performed by calculating the value of margin of exposure (MoE), which for benzo(a)pyrene and for sum of 4 PAHs were above 25,000 in both considered: mean and high exposure scenario. Studied diets were a source of exposure to PAHs. Higher levels have been reported for light, less toxic PAH as compared to heavy PAH. In both considered scenarios margin of exposure were >25 000. In case of studied diets no risk for consumer was found.

Polycyclic Aromatic Hydrocarbons and the Risk of Kidney Stones in US Adults: An Exposure-Response Analysis of NHANES 2007-2012.

BackgroundPolycyclic aromatic hydrocarbons (PAHs) exposure may cause various diseases. However, the association between PAHs exposure and kidney stones remains unclear. The purpose of this study was to examine the relationship between PAHs and the risk of kidney stones in the US population.MethodsThe study included a total of 30,442 individuals (≥20 years) from the 2007–2012 National Health and Nutrition Examination Survey (NHANES). Nine urinary PAHs were included in this study. Logistic regression and dose–response curves were used to evaluate the association between PAHs and the risk of kidney stones.ResultsWe selected 4385 participants. The dose–response curves showed a significant positive association between total PAHs, 2-hydroxynaphthalene, 1-hydroxyphenanthrene, 2-hydroxyphenanthrene, 9-hydroxyfluorene and the risk of kidney stones after adjusting for confounding factors. Compared with the low group, an increased risk of kidney stones was observed in the high group of total PAHs [OR (95% CI), 1.32 (1.06–1.64), P=0.013], 2-hydroxynaphthalene [OR (95% CI), 1.37 (1.10–1.71), P=0.005], 1-hydroxyphenanthrene [OR (95% CI), 1.24 (1.00–1.54), P=0.046] and 9-hydroxyfluorene [OR (95% CI), 1.36 (1.09–1.70), P=0.007].ConclusionHigh levels of PAHs were positively associated with the risk of kidney stones in the US population.