Benzo[a]pyrene Removal Research Articles

Removal of benzo[a]pyrene by a highly degradable microbial community immobilized by modified wheat straw biochar.

Benzo[a]pyrene (BaP), a high-molecular-weight polycyclic aromatic hydrocarbon (HMW-PAHs), is a prevalent organic pollutant. Due to various environmental factors, the viability and degradation capacity of PAHs-degrading bacteria in contaminated soil are significantly reduced. Therefore, it is imperative to maintain microbial activity and enhance degradation efficiency. This study aims to optimize BaP removal by utilizing biochar-immobilized BaP for the enhancement of microbial communities' degradative potential. The immobilization of modified wheat straw biochar (MWBC) significantly enhanced the removal efficiency of BaP by a highly efficient microbial community enriched from oil-contaminated soil, achieving a large removal efficiency of 75.18% for BaP (5-20mg/L) in a mineral salts medium in 12 d. The study also involved a detection of the species richness and intermediate metabolites of microbial community, as well as an assessment of the challenges and difficulties associated with managing real contaminated sites.

Benzo(a)pyrene degradation by the interaction of Aspergillus brasilensis and Sphigobacterium spiritovorum in wastewater: optimisation and kinetic response

ABSTRACT Benzo(a)pyrene (BaP) is a well-known environmental contaminant that poses significant risks due to its carcinogenic nature and it is crucial to remove it from the environment, especially in wastewater. Thus, this study aims to enhance the degradation of BaP in wastewater through the optimised interaction of the fungus Aspergillus brasiliensis and the bacterium Sphingomonas spiritovorum. The ideal initial pH and temperature ranges for optimising BaP breakdown were determined using response surface methodology (RSM). For that, the range of initial pH chosen was pH 4–9 and the temperature was between 25℃ – 40℃. The first-order kinetic was used to determine the kinetic response for monoculture and co-culture. The co-culture of A. brasiliensis and S. spiritovorum successfully produced a BaP removal rate of over 50%, which was much higher than the removal rates observed in monoculture treatments under optimisation conditions. The kinetic response was obtained with 0.067 d− 1 (A. brasiliensis), 0.127 d− 1 (S.spriritovorum) and 0.144 d− 1 (co-culture) for the degradation rate constant, K. The degradation half-life time, t1/2 shows the decrement for the co-culture (4.83 days) compared to monoculture. The increased degradation has been attributed to the synergistic biochemical pathways, in which fungal ligninolytic enzymes initiate the breakdown of BaP, followed by bacterial degradation of the resulting compounds. The study's results, which have been validated by Analysis of Variance (ANOVA), offer insightful information for the enhancement of bioremediation strategies. This information is practicable for researchers, practitioners, and policymakers in the context of addressing carcinogenic pollutants in wastewater.

Monodispersed FeS nanoparticles decorated on kaolinite for synchronous removal of benzo [a]pyrene and Cr(VI) complex pollution

Novel FeS/kaolinite composite (K-FeS) were successfully prepared using an in-situ precipitation method. At 30 % FeS loading, 1 g/L of the composite material by activating peroxymonosulfate (PMS) was able to completely remove 20 mg/L benzo[a]pyrene (BaP) and 40 mg/L Cr(VI) within 20 min under optimized conditions. The simultaneous removal experiments of BaP and Cr(VI) for the influence factors of BaP concentration, Cr(VI) concentration, composites dosage and PMS dosage to be 20 mg/L, 40 mg/L, 1 g/L, and 0.75 mmol/L, respectively. Experiments on environmental factors show that low temperature and acidic conditions are more favorable for material activity, and the addition of Cl- could promote the removal of BaP and Cr(VI). Comparative experiments showed that the simultaneous presence of BaP and Cr(VI) did not affect the removal of each other. The pseudo second-order kinetic model and Langmuir adsorption isotherm model were better to fit the experimental data, and the thermodynamic analyses indicated that the removal processes of BaP and Cr(VI) were spontaneous and exothermic. Besides, the quenching experiments yielded that SO4− and OH played a dominant role in BaP removal, and Cr(VI) removal mainly depended on the reduction of composites. This study expands the application of clay minerals in water treatment and suggests new strategies for simultaneous treatment of multiple pollutants in the environment.

Biodegradation and adsorption of benzo[a]pyrene by fungi-bacterial coculture

In this work, the relationship and kinetics of biodegradation and bio-adsorption of benzo[a]pyrene (BaP) by Bacillus and Ascomycota were explored, and the metabolites of BaP under mixed microbial coculture were analyzed and characterized. The results show that BaP was removed through both biosorption and biodegradation. Under mixed microbial coculture, biosorption played a significant role in the early stage and biodegradation was predominant in the later stage. During the removal of BaP, the fungi exhibited remarkable adsorption capabilities for BaP with an adsorption efficiency (AE) of 38.14 %, while bacteria had a best degradation for BaP with a degradation efficiency (DE) of 56.13 %. Under the mixed microbial culture, the removal efficiency (RE) of BaP by the synergistic action of fungi and bacteria reached up to 76.12 % within 15 days. Kinetics analysis illustrated that the degradation and adsorption process of BaP were well fit to the first-order and the pseudo-second-order kinetic models, respectively. The research on the relationship between degradation and adsorption during microbial removal of BaP, as well as the synergistic effects of fungi and bacteria, will provide a theoretical guidance for two or even synthetic microbial communities.

Vitamin C-reduced graphene oxide/Fe3O4 composite for simultaneous removal of aflatoxin B1 and benzo(a)pyrene in vegetable oils

Vegetable oils are essential constituent of the daily dietary intake. Nevertheless, they often contain aflatoxin B1 (AFB1) and benzo(a)pyrene (BAP). Physical adsorption is the most commonly used detoxification method in the vegetable oils industry. Regrettably, the previously reported adsorbents have exhibited limited efficacy, rendering them inadequate for meeting the requirements of large-scale production of edible oils. In this work, a superparamagnetic Fe3O4/reduced graphene oxide (rGO) composite was synthesized by a one-step hydrothermal method using vitamin C (VC), and systematically characterized. The Vitamin C-reduced graphene oxide/Fe3O4 composite (VC-rGO/Fe3O4) could serve as an efficient adsorbent in edible vegetable oils for the simultaneous removal of AFB1 and BAP. The results of the batch adsorption studies indicated that the pseudo-second order model and Sips model, respectively, were the best fit kinetic model and adsorption isotherm model. The adsorption of AFB1 and BAP on VC-rGO/Fe3O4 was spontaneous, which included both physical and chemical adsorption processes. The removal efficiencies of VC-rGO/Fe3O4 in 13 vegetable oils were evaluated, revealing a wide range of practical applications. Moreover, the quality and safety of detoxified vegetable oils is acceptable. Therefore, VC-rGO/Fe3O4 have been tested as promising candidates for the simultaneous removal of AFB1 and BAP in edible vegetable oils.

Effects of different precursors on the structure of lignin-based biochar and its ability to adsorb benzopyrene from sesame oil

Agricultural by-products of sesame are promising bioresources in food processing. This study extracted lignin from the by-products of sesame oil production, namely, the capsules and straw of black and white sesame. Using acid, alkali, and ethanol methods, 12 distinct lignins were obtained to prepare biochar, aiming to investigate both the structural characteristics of lignin-based biochar (LBB) and its ability to remove benzo[a]pyrene (BaP) from sesame oil. The results showed that white sesame straw was the most suitable raw material for preparing biochar. In terms of the preparation method, acid-extracted lignin biochar was more effective in removing BaP than alkaline or ethanol methods. Notably, WS-1LB (white sesame straw acid-extracted lignin biochar) exhibited the highest BaP adsorption efficiency (91.44 %) and the maximum specific surface area (1065.8187 m2/g), characterized by porous structures. The pseudo 2nd and Freundlich models were found to be the best fit for the adsorption kinetics and isotherms of BaP on LBB, respectively, suggesting that a multilayer adsorption process was dominant. The high adsorption of LBB mainly resulted from pore filling. This study provides an economical and highly efficient biochar adsorbent for the removal of BaP in oil.

Chemical inertness conversion of carbon fraction in coal gangue via N-doping for efficient benzo(a)pyrene degradation

Efficient degradation of organic pollutants in complex media via advanced oxidation processes (AOPs) is still critical and challenging. Herein, nitrogen (N)-doped coal gangue (CG) catalysts (N-CG) with economic competitiveness and environmental friendliness were successfully synthesized to activate peroxymonosulfate (PMS), exhibiting ultrafast degradation performance toward benzo(a)pyrene (BaP) with 100.00 % and 93.21 % in contaminated solution and soil under optimized condition, respectively. In addition, 0.4 N-CG possessed excellent reusability toward BaP degradation with over 80.00 % after five cycles. However, BaP removal efficiency was significantly affected by some co-existing anions (HCO3− and SO42−) and humic acid (HA) in solution and soil, as well as inhibited under alkaline conditions, especially pH ≥ 9. According to the characterizations, N-doping could promote the generation of pyridinic N and graphitic N in N-CG via high-temperature calcination, which was conducive to produce hydroxyl radical (•OH), sulfate radical (SO4•−), superoxide radical (•O2−) and single oxygen (1O2). In 0.4 N-CG/PMS system, 1O2 and •O2− were proved to be the predominant reactive oxygen species (ROSs) in BaP degradation, as well as •OH and SO4•− made certain contributions. To sum up, this work provided a promising strategy for synthesis of CG-based catalysts by chemical inertness conversion of carbon fracture via N-doping for PMS activation and opened a novel perspective for environmental remediation of hydrophobic and hydrophilic contaminants pollution.

Comparison of methods for activating sesame stalk lignin biochar for removing benzo[a]pyrene from sesame oil

In this study, three activators and two activation methods were employed to activate sesame lignin-based biochar. The biochar samples were comprehensively characterized, their abilities to adsorb benzo[a]pyrene (BaP) from sesame oil were assessed, and the mechanism was analyzed. The results showed that the biochar obtained by one-step activation was more effective in removing BaP from sesame oil than the biochar produced by two-step activation. Among them, the biochar generated by one-step activation with ZnCl2 as the activator had the largest specific surface area (1068.8776 m3/g), and the richest mesoporous structure (0.7891 m3/g); it removed 90.53 % of BaP from sesame oil. BaP was mainly adsorbed by the mesopores of biochar. Mechanistically, pore-filling, π-π conjugations, hydrogen bonding, and n-π interactions were involved. The adsorption was spontaneous and heat-absorbing. In conclusion, the preparation of sesame lignin biochar using one-step activation with ZnCl2 as the activator was found to be the best for removing BaP from sesame oil. This biochar may be an economical adsorbent for the industrial removal of BaP from sesame oil.

Mechanisms of benzene and benzo[a]pyrene biodegradation in the individually and mixed contaminated soils

There is a lack of knowledge on the biodegradation mechanisms of benzene and benzo [a]pyrene (BaP), representative compounds of polycyclic aromatic hydrocarbons (PAHs), and benzene, toluene, ethylbenzene, and xylene (BTEX), under individually and mixed contaminated soils. Therefore, a set of microcosm experiments were conducted to explore the influence of benzene and BaP on biodegradation under individual and mixed contaminated condition, and their subsequent influence on native microbial consortium. The results revealed that the total mass loss of benzene was 56.0% under benzene and BaP mixed contamination, which was less than that of individual benzene contamination (78.3%). On the other hand, the mass loss of BaP was slightly boosted to 17.6% under the condition of benzene mixed contamination with BaP from that of individual BaP contamination (14.4%). The significant differences between the microbial and biocide treatments for both benzene and BaP removal demonstrated that microbial degradation played a crucial role in the mass loss for both contaminants. In addition, the microbial analyses revealed that the contamination of benzene played a major role in the fluctuations of microbial compositions under co-contaminated conditions. Rhodococcus, Nocardioides, Gailla, and norank_c_Gitt-GS-136 performed a major role in benzene biodegradation under individual and mixed contaminated conditions while Rhodococcus, Noviherbaspirillum, and Phenylobacterium were highly involved in BaP biodegradation. Moreover, binary benzene and BaP contamination highly reduced the Rhodococcus abundance, indicating the toxic influence of co-contamination on the functional key genus. Enzymatic activities revealed that catalase, lipase, and dehydrogenase activities proliferated while polyphenol oxidase was reduced with contamination compared to the control treatment. These results provided the fundamental information to facilitate the development of more efficient bioremediation strategies, which can be tailored to specific remediation of different contamination scenarios.

Deep Eutectic Solvent Modified Surface Molecular Imprinting Polymers on Boron Nitride Sheets for Specific Recognition of the Genotoxic Impurity Benzo(a)Pyrene

As a typical genotoxic impurity (GTI), the concentration of benzo(a)pyrene (BaP) must be below the threshold of toxicological concern (TTC). However, achieving a trace BaP is a significant challenge by conventional separation media. Utilizing the unique recognition capabilities of surface molecular imprinting polymers (SMIPs), the versatility of N-vinyl-2-pyrrolidone deep eutectic solvents (NVP-DES), and the high surface area of two-dimensional nano-boron nitride (2D-nano-BN) sheets, a series of functionalized 2D-BN materials were prepared (NVP-DES-SMIP@2D-nano-BN) for the specific recognition and removal of BaP. Utilizing 2D-nano-BN sheets as the base, four NVP-DESs were employed as monomers, BaP as the template, EGDMA as the cross-linker, and BPO/DMA as the initiator to prepare NVP-DES-SMIP@2D-nano-BN. The free energy of DES was computed using Gaussian software, and characterization of NVP-DES-SMIP@2D-nano-BN was performed using Fourier transform infrared spectroscopy and transmission electron microscopy. Quantitative and qualitative determinations of BaP were conducted using high performance liquid chromatography and fluorescence. Using a recognition model, NVP-DES-SMIP@2D-nano-BN exhibited a Freundlich isotherm fit and second-order kinetics for BaP.

Composite starch films as green adsorbents for removing benzo[a]pyrene from smoked sausages

Benzo[a]pyrene (BaP), which is emitted during the processing of smoked sausages, accumulates in sausages and poses a serious threat to human health. This study focused on the removal of BaP from sausages and accompanying particulate matter (PM) during the smoking of sausages by films formed by combining corn starch (CS) with K-carrageenan (KC)/sodium alginate (SA). Initially, the effects of different additions of KC and SA on the rheological analysis, thermogravimetric analysis (TGA) and film-forming properties of the composite films were investigated. The BaP reduction capacities of CS-KC and CS-SA composite films in sausage were 41.1%-47.0% and 54.2%-56.5%, respectively, because the three-dimensional mesh structure of the composite films provided a large number of adsorption sites. Finally, kinetic studies demonstrated that BaP control in composite films is mainly achieved by intraparticle diffusion. Therefore, due to its excellent recyclability and biodegradability, composite starch film has a promising application in smoked meat products.

Important role of cosolvent addition and soil permeability on electrokinetic-persulfate remediation of benzo(a)pyrene

Benzo(a)pyrene (BaP) is a common soil pollutant that is difficult to remove from low-permeability soil. The effects of cosolvent and soil permeability on electrokinetic (EK) + persulfate (PS) remediation of BaP are not well understood. This study investigated BaP removal in two soil types of different low permeabilities (low: Soil-L; much lower: Soil-ML) under different types and concentrations of cosolvent-enhanced EK+PS remediation. In Soil-ML, BaP removal varied significantly, reaching up to 86.6% under EK+PS+ 5% hydroxypropyl-beta-cyclodextrin (HPCD) treatment. Compared to EK+PS alone, the promoting effect of HPCD on EK+PS increased with increased concentrations of HPCD; however, adding 1% Tween 80 (TW 80) suppressed BaP removal by 2.5–10.5% in the soil compared with that under EK+PS alone. The inhibition was further enhanced at 10% TW 80, with an average BaP removal of 36.2%. In contrast, in Soil-L, BaP removal was higher than in Soil-ML under EK+PS alone (additional 4.4–22.5%). Adding HPCD slightly inhibited BaP removal and adding 1% TW 80 had a slightly positive effect. PS migration (measured S2O82-) was impeded because of the low electroosmotic flow generated in Soil-ML, with higher clay, silt, and bound water contents. Overall, this study provides valuable insights into the EK remediation of polycyclic aromatic hydrocarbons in low-permeability soils.

Biodegradation of benzo(a)pyrene by a genetically engineered Bacillus licheniformis: Degradation, metabolic pathway and toxicity analysis

Benzo(a)pyrene (BaP), the polycyclic aromatic hydrocarbons (PAHs), is known for its high carcinogenic, low bioavailability, and resistance to removal. To enhance the removal efficiency of BaP, a screened BaP-dominant degrading bacterium identified as Bacillus licheniformis, was utilized to construct a genetically engineered Bacillus licheniformis, named GEM-NY2. Through successive subculturing, it was observed that the genetic stability of the first 20 generations of GEM-NY2 remained good, and the removal rate of BaP was 78.21–80.16 %. Compared to the recipient strain NY2, GEM-NY2 achieved a BaP removal rate of 78.61 %, showing a 10.36 % improvement. Then the optimal degradation parameters of the GEM-NY2 for BaP were investigated by the response surface methodology (RSM): salinity of 30 g/L, temperature of 37.5℃, pH of 6, and microbial inoculum of 3.5 %. Furthermore, UPLC-MS analysis confirmed that GEM-NY2 initiated the attack on BaP at sites C4 and C5, C7 and C8, and C9 and C10, leading to the formation of dihydroxy-BaP, then generating ring-cleavage products. Eight metabolites were obtained, and the ring-opening process of BaP by GEM-NY2 was revealed. The results of EcoSAR and acute toxicity experiments of Photobacterium phosphoreum showed as the benzene rings of BaP were cleaved, the toxicity of the metabolites gradually decreased. The luminescence inhibition rate decreased significantly from 82.89 % to 52.36 % within 14 days. In summary, the genetically engineered Bacillus licheniformis (GEM-NY2) constructed in this work exhibited promising bio-degradation potential towards BaP, highlighting its favorable prospects for the effective removal of PAHs.

Immobilization of laccase on magnetic mesoporous silica as a recoverable biocatalyst for the efficient degradation of benzo[a]pyrene

Laccase is an efficient green biocatalyst, widely used for the degradation of various organic pollutants. However, free laccase is unstable and difficult to recover, which limits its practical application. In this study, a multilayer core-shell magnetic mesoporous silica (Fe3O4@d-SiO2@p-SiO2) microsphere with high specific surface area (275 m2 g−1) was fabricated for immobilization of laccase. The unique structure of Fe3O4@d-SiO2@p-SiO2 enabled the successful immobilization of laccase. Under the optimal immobilization conditions of laccase concentration of 1.5 mg mL−1, immobilization time of 6 h, immobilization pH of 6, the loading capacity of laccase was up to 567 mg g−1. Compared with free laccase, immobilized laccase exhibited remarkable pH stability, thermal stability and storage stability. Moreover, the immobilized laccase was easy to achieve magnetic recovery and possessed excellent reusability, with its activity remaining 58.2% after 10 consecutive reuses. More importantly, immobilized laccase had good degradation performance for benzo[a]pyrene (BaP), which can achieve rapid and efficient degradation of low concentration BaP over a wide range of pH and temperature. The removal efficiency of BaP was up to 99.0% within 1 h, and still exceeded 35.0% after 5 cycles. The removal of BaP by immobilized laccase was achieved through both adsorption and degradation. The degradation products and possible degradation pathways were determined by GC-MS analysis. This study indicated that Fe3O4@d-SiO2@p-SiO2 could effectively enhance the stability and biocatalytic activity of laccase, which is expected to provide a new clean biotechnology for the remediation of BaP contaminated sites.

Effect of electric fields strength on soil factors and microorganisms during electro-bioremediation of benzo[a]pyrene-contaminated soil

Electro-bioremediation is a promising technology for remediating soils contaminated with polycyclic aromatic hydrocarbons (PAHs). However, the resulting electrokinetic effects and electrochemical reactions may inevitably cause changes in soil factors and microorganism, thereby reducing the remediation efficiency. To avoid negative effect of electric field on soil and microbes and maximize microbial degradability, it is necessary to select a suitable electric field. In this study, artificial benzo [a]pyrene (BaP)-contaminated soil was selected as the object of remediation. Changes in soil factors and microorganisms were investigated under the voltage of 1.0, 2.0, and 2.5 V cm−1 using chemical analysis, real-time PCR, and high-throughput sequencing. The results revealed noticeable changes in soil factors (pH, moisture, electrical conductivity [EC], and BaP concentration) and microbes (PAHs ring-hydroxylating dioxygenase [PAHs-RHDα] gene and bacterial community) after the application of electric field. The degree of change was related to the electric field strength, with a suitable strength being more conducive to BaP removal. At 70 d, the highest mean extent of BaP removal and PAHs-RHDα gene copies were observed in EK2.0 + BIO, reaching 3.37 and 109.62 times those in BIO, respectively, indicating that the voltage of 2.0 V cm−1 was the most suitable for soil microbial growth and metabolism. Changes in soil factors caused by electric fields can affect microbial activity and community composition. Redundancy analysis revealed that soil pH and moisture had the most significant effects on microbial community composition (P < 0.05). The purpose of this study was to determine the appropriate electric field that could be used for electro-bioremediation of PAH-contaminated soil by evaluating the effects of electric fields on soil factors and microbial communities. This study also provides a reference for efficiency enhancement and successful application of electro-bioremediation of soil contaminated with PAHs.

Degradation of benzo [a] pyrene in the soil enhanced by soapwort: The role of soapwort and functional microbial community

The limited bioavailability of polycyclic aromatic hydrocarbons (PAHs) in soils poses a challenge for their biodegradation. We hypotheses soapwort (Saponaria officinalis L.) as a factory in-situ providing biosurfactant, which could effectively promote the BaP removal by exogenous or native functional microbes. Rhizo-box and microcosm experiments were conducted to analyze the phyto-microbial remediation mechanism of soapwort, a plant that excretes biosurfactants known as saponins, and combined with two exogenous strains (P. chrysosporium and/or B. subtilis) for benzo[a]pyrene (BaP)-contaminated soils. The results revealed that the natural attenuation treatment (CK) BaP achieved only a 15.90% BaP removal rate after 100 days. In contrast, soapwort (SP), soapwort-bacteria (SPB), soapwort-fungus (SPF), soapwort- bacteria - fungus (SPM) mediated rhizosphere soils treatments yielded removal rates of 40.48%, 42.42%, 52.37%, and 62.57%, respectively. The analysis of the microbial community structure suggested that soapwort stimulated the introduction and native functional microorganisms, such as Rhizobiales, Micrococcales, and Clostridiales, which contributed to BaP removal via metabolic pathways. Furthermore, the efficient BaP removal was attributed to saponins, amino acids, and carbohydrates, which facilitated mobilization, solubilization of BaP, and microbial activity. In conclusion, our study highlights the potential of soapwort and specific microbial strains to effectively remediate PAH-contaminated soils.

The Effect of Bovine Serum Albumin on Benzo[a]pyrene Removal by Lactobacillus Strains.

The aim of this study was to investigate the influence of bovine serum albumin (BSA) on the Lactobacillus-strain-mediated removal of benzo[a]pyrene (BaP). A combination of 0.5 mg/mL of BSA with 1.0 × 1010 CFU/mL bacterial cells had a removal of 49.61% BaP for strain 121, while a combination of 0.4 mg/mL of BSA with 1.0 × 1010 CFU/mL bacterial cells had a removal of 66.09% BaP for strain ML32. The results indicated that the binding of BaP to Lactobacillus-BSA was stable. BSA maintains Lactobacillus activity and BaP removal in the gastrointestinal environment. Heat and ultrasonic treatment of BSA reduced the BaP-binding ability of Lactobacillus-BSA. With the addition of BSA, the surface properties of the two strains affected BaP binding. The Fourier-transform infrared (FTIR) data demonstrated that O-H, N-H, C=O, and P=O groups were involved in the binding of BaP to Lactobacillus-BSA. Scanning electron microscopy (SEM) results revealed that the morphology of Lactobacillus-BSA bound to BaP was maintained. The adsorption of BaP by Lactobacillus-BSA was appropriately described by the pseudo-second-order kinetic model and Freundlich isotherm model. BSA enhances the affinity between the bacterial cells and BaP.

Effects of bioaugmentation by isolated Achromobacter xylosoxidans BP1 on PAHs degradation and microbial community in contaminated soil

Polycyclic aromatic hydrocarbons (PAHs) are a group of organic pollutants ubiquitous and persistent in soil. In order to provide a viable solution for bioremediation of PAHs-contaminated soil, a strain of Achromobacter xylosoxidans BP1 with superior PAHs degradation ability was isolated from contaminated soil at a coal chemical site in northern China. The degradation of phenanthrene (PHE) and benzo[a]pyrene (BaP) by strain BP1 was investigated in three different liquid phase cultures, and the removal rates of PHE and BaP by strain BP1 were 98.47% and 29.86% after 7 days under the conditions of PHE and BaP as the only carbon source, respectively. In the medium with the coexistence of PHE and BaP, the removal rates of BP1 were 89.44% and 9.42% after 7 days, respectively. Then, strain BP1 was investigated for its feasibility in remediating PAH-contaminated soil. Among the four PAHs-contaminated soils treated differently, the treatment inoculated with BP1 exhibited higher removal rates of PHE and BaP (p < 0.05), especially the CS-BP1 treatment (inoculation of BP1 into unsterilized PAHs-contaminated soil) showed 67.72%, 13.48% removal of PHE and BaP, respectively, over 49 days of incubation. Bioaugmentation also significantly increased the activity of dehydrogenase and catalase in the soil (p＜0.05). Furthermore, the effect of bioaugmentation on the removal of PAHs was investigated by measuring the activity of dehydrogenase (DH) and catalase (CAT) during incubation. Among them, the DH and CAT activities of CS-BP1 and SCS-BP1 (inoculation of BP1 into sterilized PAHs-contaminated soil) treatments inoculated with strain BP1 were significantly higher than those of treatments without BP1 addition during incubation (p < 0.01). The structure of the microbial community varied among treatments, but the Proteobacteria phylum showed the highest relative abundance in all treatments of the bioremediation process, and most of the bacteria with higher relative abundance at the genus level also belonged to the Proteobacteria phylum. Prediction of microbial functions in soil by FAPROTAX analysis showed that bioaugmentation enhanced microbial functions associated with the degradation of PAHs. These results demonstrate the effectiveness of Achromobacter xylosoxidans BP1 as a PAH-contaminated soil degrader for the risk control of PAHs contamination.

Remediation of benzo[a]pyrene contaminated soils by moderate chemical oxidation coupled with microbial degradation

Chemical oxidation is a promising technology for the remediation of organics-contaminated soils. However, residual oxidants and transformation products have adverse effects on microbial activities. This work aimed at moderate chemical oxidation coupled with microbial degradation (MOMD) for the removal of benzo[a]pyrene (BaP) by optimizing the type and dosage of oxidants. Potassium permanganate (KMnO4), Fe2+ + sodium persulfate (Fe2+ + PS), Fenton's reagent (Fe2+ + H2O2), and hydrogen peroxide (H2O2) were compared for BaP removal from loam clay and sandy soils. Overall, the removal efficiency of BaP by a moderate dose of oxidant coupled indigenous microorganism was slightly lower than that by a high dose of relevant oxidant. The contributions of microbial degradation to the total removal of BaP varied for different oxidants and soils. The removal efficiency of BaP from loam clay sandy soil by a moderate dose of KMnO4 (25 mmol/L) was 94.3 ± 1.1 % and 92.5 ± 1.8 %, respectively, which were both relatively higher than those under other conditions. The indirect carbon footprint yielded by the moderate dose of oxidants was 39.2–72.8 % less than that by the complete oxidation. A moderate dose of oxidants also reduced disturbances to soil pH and OC. The microbial communities after MOMD treatment were dominated by Burkholderiaceae, Enterobacteriaceae, Alicyclobacillaceae, and Oxalobacteraceae. These dominant microorganisms promoted the removal of BaP through the expression of polycyclic aromatic hydrocarbon-ring hydroxylated dioxygenase gene. Compared with complete chemical oxidation, MOMD is also a promising technique with the utilization of indigenous microorganism for remediating BaP-contaminated soils.

Optimization Method to Determine the Kinetic Rate Constants for the Removal of Benzo[a]pyrene and Anthracene in Water through the Fenton Process

The reaction rate constants concerning the removal of benzo[a]pyrene (BaP) and anthracene (AN) in water by the Fenton process can be commonly found from the experimental data and by using regression models. However, this calculation is a time-consuming and a difficult task. Therefore, an algorithm for the determination of the rate constants depletion of the pollutants of interest should be developed. In this study, several algorithms were developed, using MATLAB® software for representing AN and BaP elimination by the Fenton process under an experimental domain. These algorithms were derived from the first-, second- and third-order kinetic models, as well as from the double exponential and the Behnajady-Modirshahla-Ghanbery (BMG) kinetic models. Regarding the AN and BaP removal kinetics, the double exponential and the BMG models were found to exhibit the highest correlation coefficients (&gt;0.98 and &gt;0.95, respectively) in comparison with those ones obtained from the first-, second- and third-order kinetic models (&gt;0.80, &gt;0.85 and &gt;0.88, respectively). It was found that the algorithms can be used to optimize and fit the rate constants by creating an objective function that fits and represents the experimental data obtained concerning the removal of the compounds of interest through the Fenton advanced oxidation process.