Occurrence and Source Apportionment of Polycyclic Aromatic Hydrocarbons in Urban Residential Soils from National Capital Region,Uttar Pradesh,India

This study aims to investigate the level of priority polycyclic aromatic hydrocarbons (PAHs) and identification of their potential sources in residential soils. During the study, a total 36 soil samples collected from twelve residential locations at Sahibabad-Ghaziabad area of western Uttar Pradesh, India, a constituted part of the National Capital Region of India. Samples extracted using ultrasonication, cleaned with silica and analyzed by diode array detector–high-performance liquid chromatography using acetonitrile/water as mobile phase. The 25th and 75th percentile concentration of ∑PAHs was 264 μg kg^?1 and 584 μg kg^?1, respectively, with mean and median of 445 μg kg^?1 and 421 μg kg^?1. The detection frequency of PAHs in all samples was lower for low molecular weight PAHs (19%) than high molecular weight PAHs (81%). The concentration of seven probable carcinogenic PAHs accounted for 67% of the ∑PAHs. PAHs toxicity potential as benzo(a)pyrene toxicity equivalent ranged between 2.52–253 μg BaP_TEQ kg^?1. Composition profile of PAHs with different aromatic rings and selected diagnostic molecular ratios suggested the local pyrogenic sources of PAHs from vehicular emissions, diesel engines, biomass combustion, gasoline, and coal combustions.     

Evaluation of polyaromatic hydrocarbon removal from aqueous solutions using activated carbon and hyper‐crosslinked polymer (Macronet MN200)

BACKGROUND: Sorption of polycyclic aromatic hydrocarbons (PAHs) on activated carbon and the Macronet polymeric sorbent MN200 was investigated to determine the effectiveness of each sorbent for removal of pollutants from aqueous solution and their possible use as sorbent materials for groundwater. Experiments were carried out to determine the loading capacities of a family of PAHs (acenaphthene, anthracene, fluoranthene, fluorene, naphthalene and pyrene). RESULTS: Activated carbon was the more effective sorbent, with maximum loadings of PAHs between 90 and 230 g kg^?1, while MN200 resin showed values of 25–160 g kg^?1. Loading isotherms based on the Langmuir, Freundlich and Redlich–Peterson models were determined. The hydrophobic character of the pollutants appeared as an important parameter related to the sorption process. Equilibrium and kinetic parameters were used to determine the retardation factors for each PAH. CONCLUSION: The calculated values for the simulation of barrier thickness using both sorbents, taking into account EU requirements for PAHs in groundwater effluent, were perfectly reasonable as a first estimate. The better kinetic properties of MN200 are evident in lower hydraulic residence times and consequently in a lower barrier thickness. Copyright © 2008 Society of Chemical Industry     

Polycyclic Aromatic Hydrocarbons in Residential Soils from an Indian City near Power Plants Area and Assessment of Health Risk for Human Population

This article deals with the distribution, composition profiles, and possible sources of sixteen priority polycyclic aromatic hydrocarbons (PAHs) in residential soils from Korba district in Chhattisgarh State, India. Sixteen priority PAHs in soils were analyzed after ultrasonic extraction, silica gel column chromatographic cleanup, and quantitation was performed using HPLC-DAD. The concentrations of ∑16PAHs were within acceptable limits of soil quality guidelines and the study area got classified as weakly contaminated. The concentration of probable human carcinogenic PAHs in soils accounted for 10% of ∑16PAHs. The concentration of Benzo(a)Pyrene (BaP) accounted 1% to total PAHs. Benzo(a)pyrene Toxicity Equivalency (BaP_TEQ) for 16 PAHs was 30 ± 12 μg BaP_TEQ kg^?1. The composition profiles and molecular ratios of PAHs suggested mixed pyrogenic sources of PAHs from combustion of coal, wood, and vehicular exhaust emissions. Human health risk was assessed by calculating the lifetime average daily dose (LADD) and incremental life time cancer risk (ILCR) for human adults and children. Estimated ILCR was within safe limit (10^?6?10^?5), indicating low risk to human population. Potential risk to contaminated ground water from leaching of carcinogenic PAHs was assessed by estimating the Index of Additive Cancer Risk (IACR).     

Polycyclic Aromatic Hydrocarbons,Heavy Metals,and Genotoxicity of the Suburban Soils from Guangzhou,China

During the past few decades, urban and suburban developments have grown at unprecedented rates and extents with unknown consequences for ecosystem function. The problem of soil pollution as a result of the accelerating development of Guangzhou in China is becoming great concerns. In the present study, gas chromatograph coupled mass spectrometry (GC-MS), inductively coupled plasma mass spectrometry (ICP-MS) and inductively coupled plasma atomic emission spectrometry (ICP-AES) were employed to determine the 16 US Environmental Protection Agency (EPA) priority polycyclic aromatic hydrocarbons (PAHs) and the heavy metals (As, Cr, Cu, Pb, Cd, Hg, and Se) of soils collected from suburban areas of Guangzhou. The genotoxicity of these soils was screened with micronucleus (MN) assay in Vicia faba root cells. The concentrations of the pollutants in the soils were (dried weight): ΣPAHs (230.6–1263 ng·g^?1), As (2282.6–36064 μg·kg^?1), Cr (7109–64699 μg·kg^?1), Cu (7047–56388 μg·kg^?1), Pb (9675.9–93739 μg·kg^?1), Cd (68.5–847.3 μg·kg^?1), Hg (85.4–549.2 μg·kg^?1), and Se (219.2–968 μg·kg^?1), which fell in the moderately polluted range. However, six out of nine soil-exposed groups had a significant increases of MN frequencies observed in the V. faba root cells compared with the negative group (P < 0.05, P < 0.01), indicating that they had potential genotoxic risks. Bringing together the chemical analyses with the biological effects observed in this study, the genotoxic response could at a certain degree be explained by both the soil PAHs and heavy metals. Our results suggested that apart from chemical analysis, bioassays like the MN assay of V. faba root cells should also be included in a battery of tests to assess the eco-environmental risks of urban and/or urbanization in the developing areas on the soils.     

Polycyclic Aromatic Hydrocarbons and Nitropolycyclic Aromatic Hydrocarbons in Atmospheric Particles and Soil at a Traffic Site in Hanoi,Vietnam

The concentrations of polycyclic aromatic hydrocarbons (PAHs) and nitropolycyclic aromatic hydrocarbons (NPAHs) in total suspended particulates (TSP) and soil were measured at a traffic site in Hanoi, a typical motorcycle city of Vietnam. TSP was collected using high-volume air sampler on Pallflex 2500QAT-UP membrane filters. PAHs and NPAHs were analyzed by high-performance liquid chromatography (HPLC) using fluorescence and chemiluminescence detectors, respectively. The average concentrations of total 10 PAHs and 10 NPAHs in soil varied from 3.4–43.7 ng g^?1 and from 112–780 pg g^?1 dry weight, respectively, which were much lower than those in TSP. The results showed that large part of the higher molecular weight PAHs in soil, especially benzo[ghi]perylene and benzo[b]fluoranthene came from the atmosphere. However, NPAHs profile showed a different pattern. 3-nitroperylene and 6-nitrochrysene were the most abundant NPAHs in soil, followed by 1-nitropyrene and 6-nitrobenzo[a]pyrene. The fate of NPAHs in soil varied depending on soil properties and chemical structure of NPAHs. The finding that the [NPAH]/[PAH] concentration ratios in soil were different from those in TSP could be due to bio-degradation and/or secondary formation of NPAHs in soil, depending on NPAHs properties.     

Indoor Polycyclic Aromatic Hydrocarbon Concentration in Central India

The indoor burning of different materials like fuels, incense, mosquito coil, candles etc. results in generation of polycyclic aromatic hydrocarbons (PAHs) in an uncontrolled manner. The PAH, i.e., Benzo(a)pyrene (BaP) is considered as most toxic or carcinogenic and the toxicity of other PAHs is related to this compound. Therefore, the concentration and emission fluxes of polycyclic aromatic hydrocarbons (PAHs) emitted during burning of commonly used indoor materials, i.e., 15 fuels (i.e., biomass (BM), coal (C), cow dung (CD), kerosene (K)), 4 incense (IS) and mosquito coil (MC) in Raipur district, Chhattisgarh, central India is described. The samples were taken in September 2013 in indoor environments and respective smoke emitted were collected using high volume United State of America (USA) air sampler on quartz fiber filters. The concentration of total 13 PAHs (∑PAH₁₃) (i.e., phenanthrene, anthracene, fluoranthene, pyrene, benz(a)anthracene, chrysene, benzo(b)fluoranthene, benzo(k)fluoranthene, benzo(a)-pyrene, dibenz(ah)anthracene, benzo(ghi) perylene, indeno1,2,3-(cd)pyrene, and coronene) in particulate matter (PM₁₀) in the indoor air during burning of the fuels, IS and MC materials ranged from 367–92052 ng m^?3, 4089–14047 ng m^?3, and 66–103 ng m^?3 with mean values of 7767 ± 11809 ng m^?3, 9977 ± 4137 ng m^?3, and 74 ± 20 ng m^?3, respectively. The mean concentration of the ∑PAH₁₃ present in indoor environment is much higher than the WHO limit value of 1.0 ng m^?3. The sources and toxicities of PAHs are discussed.     

Analysis by GC-MS of Polycyclic Aromatic Hydrocarbons in a Cream Containing Coal Tar

Qualitative and quantitative PAHs composition of a cream containing coal tar (5%), used in cutaneous diseases treatment, was studied. Eleven PAHs were analysed in pure coal tar and in the cream by GC-MS, after ultrasonic extraction by pyridine. Ten PAHs were found in pure coal tar: naphthalene, biphenyl, acenaphthylene, fluorene, phenanthrene, anthracene, carbazole, fluoranthene, pyrene and benzo[a]pyrene. No traces of 2,3-benzofluorene were detected. Seven PAHs were identified in the cream: naphthalene, biphenyl, acenaphthylene, fluorene, phenanthrene, fluoranthene and pyrene. 2,3-benzofluorene was also absent in the cream. Anthracene, carbazole and benzo[a]pyrene (one of the most toxic) were present in coal tar and not detected in the cream.

The seven PAHs found in the cream and in coal tar were quantified. Hydrocarbons concentrations were between 0.107 ± 0.0038 mg.g^?1 (for biphenyl) and 0.734 ± 0.0438 mg.g^?1 (for phenanthrene) in the cream and between 4.31 ± 0.23 mg.g^?1 (for biphenyl) and 21.9 ± 0.57 mg.g^?1 (for fluorene) in coal tar.     

OPTIMIZATION OF LARGE VOLUME INJECTION FOR IMPROVED DETECTION OF POLYCYCLIC AROMATIC HYDROCARBONS (PAH) IN MUSSELS

Detection of PAH of six benzene rings is somewhat troublesome and lowering the limits of detection (LODs) for these compounds in food is necessary. For this purpose, we optimized a Programmable-Temperature-Vaporisation (PTV) injection with Large Volume Injection (LVI) with regard to the GC-MS detection of anthracene, benz[a]anthracene, benzo[a]pyrene, indeno[1,2,3-cd]pyrene and dibenzo[a,e]pyrene. The optimization of PTV-LVI for GC-MS analysis included the choice of liner, solvent venting, splitless time, split flow and initial inlet temperature for injection of 25 μ L standard solution and spiked mussel samples. Samples were extracted with Accelerated Solvent Extraction (ASE) followed by two semi-automatic clean-up steps; gel permeation chromatography (GPC) on S-X3 and solid phase extraction (SPE) on pre-packed silica columns, prior to gas chromatography-mass spectrometry (GC-MS) detection. In comparison to traditional splitless injection, LODs were lowered for eighteen PAHs by the use of PTV-LVI ranging from 0.05 μ g kg ^?1 to 1.0 μ g kg^?1 fresh weight. In particular, the LOD of dibenzo[a,e]pyrene was improved by a factor of ten when using the validated PTV-LVI method.     

Aerobic biodegradation and inhibition kinetics of poly‐aromatic hydrocarbons (PAHs) in a petrochemical industry wastewater in the presence of biosurfactants

BACKROUND: In Izmir, Turkey, wastewaters from the petrochemical industry are treated using conventional activated sludge systems. A significant proportion of poly‐aromatic hydrocarbons (PAHs) with high‐molecular weights remains in this treatment system and inhibits the biological activity. Biosurfactants increase PAHs degradation by enhancing the solubility of the petroleum components. The aerobic inhibition kinetics of PAHs has not previously been investigated in the presence of biosurfactants for a real petrochemical industry wastewater. RESULTS: Among the kinetic models used (Monod‐type, zero, first‐order and second‐order) it was found that the Monod kinetic was effective for describing the biodegradation of PAHs in petrochemcal industry wastewater in the presence of three biosurfactants, namely Rhamnolipid (RD), Surfactine (SR) and Emulsan (EM) in an aerobic activated sludge reactor (AASR). The maximum PAH removal rate (R_max) and specific growth rate of PAH degrading bacteria (µ_max) increased, while the half saturation concentration of PAH (K_s) decreased at 15 mg L^?1 RD concentration compared with the control without biosurfactant at a sludge retention time (SRT) of 25 days. CONCLUSION: PAH oxidation is typified by competitive inhibition at RD concentrations > 15 mg L^?1 resulting in increases in K_s values with PAH accumulation. Low inhibition constant (K_ID) values reflect difficulties in the metabolizability of PAHs. Metabolite production decreased at RD = 25 mg L^?1 in the PAHs indeno (1,2,3‐cd) pyrene (IcdP), flourene (FLN), phenanthrene (PHE) and benzo(a)pyrene (BaP). Copyright © 2011 Society of Chemical Industry     

焦化厂土壤中PAHs的累积、垂向分布特征及来源分析

引言多环芳烃(polycyclic aromatic hydrocarbons,PAHs)在环境中普遍存在,由于具有强烈的诱变、致癌和致畸作用而受到越来越多的关注。以煤为主要原料的焦化行业,是环境中人类活动产生PAHs的主要来源之一,其各个生产车间内化石燃料的不完全燃烧及焦油、煤气等化工产品的加工过程都可能导致PAHs的排放。土壤是PAHs累积和迁移的重要介质,环境中的PAHs可由大气     

Bioremediation of Polycyclic Aromatic Hydrocarbon Contaminated Soil by a Microbial Consortium through Supplementation of Biosurfactant Produced by Pseudomonas aeruginosa Strain

Lipopeptide biosurfactant produced by Pseudomonas aeruginosa Lbp 3 strain isolated from petroleum contaminated soil was investigated for its potential to enhance bioavailability, and hence, the biodegradation of polycyclic aromatic hydrocarbons (PAHs) in contaminated soil microcosms. Experiments were conducted on a soil spiked with equal parts of the PAHs Phenanthrene, Fluoranthene, and Pyrene to a final concentration of 1200 mg of total PAHs per kg of dry soil. To evaluate biodegradation enhancement efficiency, 50 g spiked soil samples were supplemented with 50 mgL^?1, 100 mgL^?1, 300 mgL^?1, and 1000 mgL^?1of lipopeptide dissolved in 30 mL of MSM, and incubated for 40 days at 30°C in darkness. Statistically significant (P < 0.05) biodegradation rates were observed in all the amended microcosms in comparison to the unamended controls. Maximal biodegradations (> 96% of Phenanthrene and Fluoranthene and > 93% of Pyrene) were observed in the soil microcosms supplemented with 1000 mgL^?1and 50 mgL^?1 lipopeptide. The effect of substrate interactivity of the PAHs on the biodegradation kinetics was also tested in comparison with sole substrate microcosms. Competitive inhibition of the biodegradation of low molecular weight PAHs was observed as a result of substrate interactivity in the multisubstrate system.     

Ozonation of Polycyclic Aromatic Hydrocarbons in Water Solution

The degradation of three polycyclic aromatic hydrocarbons (PAHs): benzo[a]pyrene (BAP), chrysene (CHR), and fluorene (FLU) in aqueous solution using ozone was investigated. The influence of pH of the reaction mixture, ozone concentration, and the presence of a radical scavenger on the reaction rate was determined. The highest rate of PAHs disappearance was achieved in acidic solutions. The radical scavenger, tert-butanol, effectively inhibited the rate of PAHs destruction. The rate constants of direct reaction of PAHs with ozone were calculated and they were equal to (3.32 ± 0.21) × 10⁴; (1.10 ± 0.15) × 10⁴ and 44.8 ± 1.1 M^?1s^?1 for BAP, CHR, and FLU, respectively. The contributions of direct ozonolysis, and radical reaction to PAHs oxidation in ozonation processes, were evaluated.     

LONG TERM MONITORING OF POLYCYCLIC AROMATIC HYDROCARBONS (PAHS) IN BLUE MUSSELS (Mytilus edulis) FROM A REMOTE SCOTTISH LOCATION

Farmed mussels have been collected on a monthly basis since 1999 from a remote site on the west coast of Scotland for polycyclic aromatic hydrocarbon (PAHs) analysis with the aim of establishing background concentrations as a benchmark against which to assess any environmental incident. Total PAH (2- to 6-ring parent and alkylated) concentrations ranged from 12.5 to 151.2 μg kg^?1 wet weight. Seasonal trends were evident with concentrations being significantly higher for samples collected between November and March compared to those collected between April and October. By taking the median of medians for each of these time periods two background concentrations are suggested for the total PAH concentrations (2- to 6-ring PAHs parent and alkylated); for April to October: 31.2 μg kg^?1 wet weight and for November to March: 62.9 μg kg^?1 wet weight. Individual PAH concentrations were mainly below the OSPAR Background Assessment Concentrations (BACs), where they are specified, and were only exceeded for the heavier 4- and 5-ring PAHs (fluoranthene, pyrene, benz[a]anthracene and benzo[a]pyrene) in samples collected between November and March. Differences were also seen in the PAH profiles with season. Mussels collected between November and March had a higher proportion of the heavier PAHs compared to mussels collected in the summer and autumn.     

Bisphenol A—A Dangerous Pollutant Distorting the Biological Properties of Soil

Bisphenol A (BPA), with its wide array of products and applications, is currently one of the most commonly produced chemicals in the world. A narrow pool of data on BPA–microorganism–plant interaction mechanisms has stimulated the following research, the aim of which has been to determine the response of the soil microbiome and crop plants, as well as the activity of soil enzymes exposed to BPA pressure. A range of disturbances was assessed, based on the activity of seven soil enzymes, an abundance of five groups of microorganisms, and the structural diversity of the soil microbiome. The condition of the soil was verified by determining the values of the indices: colony development (CD), ecophysiological diversity (EP), the Shannon–Weaver index, and the Simpson index, tolerance of soil enzymes, microorganisms and plants (TI_BPA), biochemical soil fertility (BA₂₁), the ratio of the mass of aerial parts to the mass of plant roots (PR), and the leaf greenness index: Soil and Plant Analysis Development (SPAD). The data brought into sharp focus the adverse effects of BPA on the abundance and ecophysiological diversity of fungi. A change in the structural composition of bacteria was noted. Bisphenol A had a more beneficial effect on the Proteobacteria than on bacteria from the phyla Actinobacteria or Bacteroidetes. The microbiome of the soil exposed to BPA was numerously represented by bacteria from the genus Sphingomonas. In this object pool, the highest fungal OTU richness was achieved by the genus Penicillium, a representative of the phylum Ascomycota. A dose of 1000 mg BPA kg⁻¹ d.m. of soil depressed the activity of dehydrogenases, urease, acid phosphatase and β-glucosidase, while increasing that of alkaline phosphatase and arylsulfatase. Spring oilseed rape and maize responded significantly negatively to the soil contamination with BPA.     

微生物作用下多环芳烃在土壤中的迁移特征

以菲、蒽和芘为研究对象,通过淋溶实验考察抑菌和未抑菌条件下三者在土壤中的迁移过程,结果表明,微生物的存在抑制PAHs淋出:抑菌条件下180 d时菲、蒽和芘的淋出率分别为8.74%、28.53%和13.56%,未抑菌条件下240 d时菲、蒽和芘的淋出率分别为0.95%、1.47%和0.37%。抑菌和未抑菌条件下3种PAHs均易吸附于表层土壤中:淋滤240 d时,约75%的菲分布在进水端0~2 cm;超过90%的蒽分布在进水端10 cm以内;85%的芘分布在4 cm以内;微生物通过阻滞作用和降解作用影响PAHs的迁移,菲、蒽和芘在土壤中都能被土著微生物降解;60 d以前土柱中PAHs降解以好氧降解为主,60 d以后,PAHs的生物降解转为厌氧降解。     

Determination of Polycyclic Aromatic Hydrocarbons in Water- and Gin-Based Tea Infusions of Selected Tea Brands in Nigeria

The concentrations of the 16 priority polycyclic aromatic hydrocarbons (PAHs) in tea infusions made of water and local gin (alcohol) were investigated with a view to providing information on the profiles and health hazards associated with these two common Nigerian methods for tea consumption. The water-based tea infusion was prepared by submerging 4 g of tea in boiling water and allowing it to stand for 15 min, while the gin-based infusion was simply prepared by submerging 4 g of tea in gin at room temperature and allowing it to stand for 15 min. The concentrations of the ∑16 PAHs in the infusions were measured by using gas chromatography equipped with a flame ionization detector (GC-FID) after ultrasound-assisted extraction and clean-up. The concentrations of the ∑16 PAHs ranged from 24.9–623.4 μg kg^?1 with a mean value of 177 μg kg^?1 and 36.8–438.3 μg kg^?1 with a mean of 189 μg kg^?1 for water- and local gin-based infusions, respectively. The concentration of the ∑16 PAHs in the water- and local gin-based infusions of these teas were high when compared with levels reported in the literature for tea infusions. The local gin-based infusions had a higher mean level of the ∑16 PAHs than the water-based infusions. Four- and five-ring PAH compounds were dominant in these tea infusions.     

POLYCYCLIC AROMATIC HYDROCARBONS ANALYZED IN RAINWATER COLLECTED ON TWO SITES IN EAST OF FRANCE (STRASBOURG AND ERSTEIN)

Polycyclic Aromatic Hydrocarbons (naphtalene, acenaphtene, fluorene, phenanthrene, anthracene, fluoranthene, pyrene, benzo[a]anthracene, chrysene, benzo[j]fluoranthene, benzo[b]fluoranthene, benzo[k]fluoranthene, benzo[a]pyrene, dibenzo[a,h]anthracene, benzo[g,h,i]perylène, indeno[1,2,3-c,d]pyrene and coronene) have been consecutively analyzed in rainwater sampled in Strasbourg (urban site) and Erstein (rural site) between January 2002 and June 2003 and between April 2002 and June 2003 on a weekly basis respectively. For the sampling of rainwater, a wet-only rainwater sampler was used together with an open collector to take the measurements of precipitation.

PAHs in rainwater were extracted by using SPE cartridges and analyzed by HPLC-fluorescence following a method developed in the laboratory.

Mean concentrations of all PAHs (Σ 16 HAPs) varied between 0.15 and 79.60 ng·L^?1 in Erstein, and between 3.70 and 1596.45 ng·L^?1 in Strasbourg. Naphtalene, phenanthrene, fluoranthene, pyrene, chrysene, benzo[j]fluoranthne and benzo[a]pyrene were the most concentrated PAHs analyzed. Benzo[a]pyrene was frequently detected. Seasonal effects were observed with a maximum of concentrations of PAHs during cold periods. Some spatial influences were also reported. The calculation of some PAH ratios show that diesel exhaust could be the main source of PAHs in rainwater on the two sites.     

Status of PAHs in Environmental Compartments of South Africa: A Country Report

This article covers the status of PAH concentrations and composition patterns in surface water, air, sediment, and soil samples from South Africa. Despite South Africa being one of the largest economies in Africa, it is only recently that researchers have reported the presence and possible sources of these compounds in various environmental compartments. This article discusses the potential hotspots and possible sources of these compounds. It also compares the total PAH concentrations and percentage composition patterns of the individual PAHs. So far, total concentrations of five PAHs determined in sediment samples from the Johannesburg area, Gauteng Province, gave the highest concentrations ranging from 1233–136,276 μg kg^?1. The total concentration of six PAHs found in runoff water from the Venda region of the Limpopo Province, gave the highest concentration with a range of 28.7–3192.6 μg L^?1. The decreasing order of percentage composition of PAHs in water samples tended to follow 3-ring > 4-ring > 2-ring PAHs. In soil samples the decreasing order of percentage composition followed 4-ring > 3-ring > 5-ring > 2-ring > 6-ring PAHs. The total freely dissolved PAHs followed solubility of the compounds with 2-ring > 3-ring > 4-ring > 5-ring > 6-ring PAHs. Some of the identified sources of PAHs using molecular ratios include petrogenic emissions such as from petroleum combustion from vehicles and pyrolytic sources such as coal combustion by coal powered power stations, as well as iron and steel production industries. Oil spills were also identified as major PAH contributor in runoff water from the Venda region of the Limpopo Province.     

Source Allocation of Aliphatic and Polycyclic Aromatic Hydrocarbons in Particulate-Phase (PM10) in the City of Valdivia,Chile

The concentration and signature of n-alkanes (n-C₁₀ to n-C₃₃) and 18 PAHs were determined in air filters across a year period (2010) in an urban area of the city of Valdivia, Chile. Filter samples were extracted using sohxlet apparatus and analyzed by GC-MS techniques. Concentrations of total hydrocarbons ranged from 45–352 ng.m^?3 and total PAHs ranged from 2.93–78.01 ng.m^?3. Concentrations of hydrocarbons during the summer were high (288–352 ng.m^-3) and reduced when the autumn began (45–79 ng.m^?3) to then increase almost linearly to the next summer. The drop in concentration was attributed in part to the significant reduction of traffic when summer ends as tourists leave the city (about 9–15% of the total cars circulating). Results from the chemometric technique of Polytopic Vector Analysis (PVA) indicated three main sources for the alkanes: biogenic (terrestrial plants), signatures of oil combustion, and an unconfirmed source which is thought to come from non specific organic matter degradation. Total PAHs correlated well with total particulate matter with a R² = 0.94. Levels of PAHs in the atmosphere were higher during the winter (6.85–78.01 ng.m^?3) period than the rest of the year (2.93–36.30 ng.m^?3). PVA results indicate three key sources of PAHs and two of those sources derived from oil combustion and biomass burning.     

Use of Surfactants to Enhance the Removal of PAHs from Soil

The efficiency of soil remediation is often limited by the low aqueous solubility of Polycyclic Aromatic Hydrocarbons, PAHs. Surfactants can then be used to enhance the removal of PAHs from soils. The dissolution of pure solid deposit of benzo(a)pyrene, B(a)P, has shown that cationic surfactants are the most efficient to increase the aqueous solubility of B(a)P, when compared to neutral or anionic surfactants. In this paper we compare by using soil suspension washings, the efficiency of two surfactants (i) a cationic surfactant, the benzyldimethyl dodecylammonium bromide, BDDA, and (ii) a neutral one, the t-octylphenoxypolyethoxy ethanol, triton X-100. The losses of surfactant, by adsorption on soil or precipitation, were measured together with the release of B(a)P, chosen as a model molecule, representative of all the PAHs. The efficiency of surfactants used in blend was then compared to the efficiency of surfactants alone.