Benzene Compounds Research Articles

Microplastics and their interaction with microorganisms in Bosten Lake water

Microplastic pollution in inland freshwater lakes, formed from melting ice, atmospheric precipitation, and groundwater, remains under-researched. This study examines microplastic (MPS) presence and distribution in Bosten Lake and their interaction with microorganisms. We employed a Confocal Raman spectrometer to identify MPS types and 16S rRNA high-throughput sequencing to analyze microbial diversity and composition. In May, the lake's average microplastic concentration was 108.20 particles per liter (PCS/L), decreasing to 21.67 PCS/L by October. Transparent and yellow fibrous microplastics, predominantly 0.2–0.5 mm in size, were most common. Key microplastics in May included PEEK (27%), PMMA (25%), and PET (9%), while October saw a prevalence of PET (35%), PS (13%), and PA (9%). Higher microplastic concentrations correlated with reduced microbial diversity. In May, the high microplastic concentration group (MH) showed increased Planctomycetota, while in October, Patescibacteria and Bacteroidota rose significantly in the high plastic group (OH), known for microplastic degradation. MH also had a higher abundance of Cryptomycota compared to OH. Functional analysis indicated that MH had more genes related to bisphenol, benzene, and chlorine compounds, whereas OH had genes linked to methane, nitrogen, and organic matter degradation. Microplastic concentrations peaked near the lake inlet and tourist areas, affecting microbial quantity, diversity, structure, and function. This research enhances our understanding of MPS distribution and environmental microbial shifts in similar settings, providing essential data for environmental management strategies at Bosten Lake.

Accurate low-dose exposure assessment of benzene and monoaromatic compounds by diffusive sampling: Sampling and analytical method validation according to ISO 23320 for radiello® samplers packed with graphitised charcoal and suitable for thermal desorption

This research was aimed at providing an accurate low-dose benzene exposure assessment method, prospectively suitable to exposure limit values in the low ppb range, such as in the present-day chemical, petrochemical, foundry and pharmaceutical industry. The project addresses the need for a robust and fully validated method of personal exposure measurements considering that the Occupational Exposure Limit Value for benzene will be significantly lowered in the next few years. Diffusive sampling offers a reliable alternative to pumped sampling methods, intrinsic safety in potentially explosive atmospheres, lightness and ease of use. The tested diffusive sampler is radiello® with the RAD145 adsorption substrate. This configuration is packed with graphitised charcoal suitable for thermal desorption and analysis by HRGC-FID or HRGC-MS.The experiments have been conducted following the ISO 23320 standard in the range from 0.005 to 0.1 ppm (16 to 320 µg/m3), yielding a full validation of the sampling and analytical method. The sampler performances have fulfilled all requisites of the ISO 23320 standard, in particular: bias due to the selection of a non-ideal sorbent is lower than 10 % (no significant back diffusion of benzene due to concentration change in the atmosphere); bias due to storage of samples for up to 2 months is lower than 10 %; nominal uptake rate for benzene on RAD145 is 32.3 mL/min; expanded uncertainty of the sampling and analytical method is 22.1 % in the concentration range from 80 to 320 µg/m³. The sampling and analytical method is therefore fit-for-purpose for the personal exposure measurements aimed at testing compliance with lowered occupational exposure limit values for benzene. The method is also fit for short duration exposure monitoring related to specific tasks, and other volatile organic compounds, usually found in the same workplaces, such as aliphatic and aromatic hydrocarbons and some oxygenated compounds, have been also studied. In particular, n-hexane and isopropyl benzene (also known as cumene), whose classification is currently under revision, can be efficiently monitored by this technique.

In vitro spectroscopic analysis of the chemical interaction between calcium hypochlorite and chlorhexidine.

This study aimed to identify the chemical composition resulting from the chemical interaction between calcium hypochlorite [Ca(OCl)2] and chlorhexidine (CHX) using different 1H and 13C nuclear magnetic resonance spectrometry (NMR), correlated two-dimensional spectroscopy (2D COSY), heteronuclear single quantum coherence (HSQC), and Fourier Transform Infrared Spectroscopy (FTIR) experiments. The 5.25% Ca(OCl)2 was mixed with 2% CHX in a 1:1 ratio, obtaining an orange-brown precipitate that was filtered, washed in ultrapure water, dried and characterized by 1H and 13C NMR, 2D COSY, HSQC and FTIR. One-dimensional and two-dimensional NMR spectra demonstrated the chemical changes around the protons and carbon atoms of the initial CHX and after reacted with Ca(OCl)2. These techniques and FTIR show that the interaction generated two by-products from the degradation of CHX, none of which were parachloroaniline (PCA) despite both products obtained being substituted benzene compounds. Using NMR and FTIR data together with a previously proposed catalytic cleavage degradation mechanism for CHX, the products appear to be parachlorophenylurea (PCU) and parachlorophenylguanidyl-1,6-diguanidyl-hexane (PCGH). Therefore, this in vitro study demonstrated that the precipitate formed from the chemical interaction between Ca(OCl)₂ and CHX results in two by-products, PCU and PCGH, neither of which is PCA. Due to the absence of cytotoxicity studies on the products generated from the combination of Ca(OCl)₂ and CHX, an intermediate rinse with an inert solution is recommended to remove these compounds from the root canals.

Emission Risk and Inhibition Technology of Asphalt Fume from Crumb Rubber Modified Asphalt

Crumb rubber-modified asphalt mixtures have been proven to have extensive utilization value in road engineering. However, the rubber releases more fumes during the construction period, which causes severe harm to human health and the environment. This research focused on the emission risk of asphalt fume from crumb rubber-modified asphalt, and then the inhibition technology was also optimized. Firstly, the emission behavior and the hazardous evaluation of the asphalt fume from crumb rubber-modified asphalt were investigated. Then, the characteristics of the inhibition materials were evaluated. Finally, the reduction in the emission of inhibited crumb rubber-modified asphalt fume was identified, and the optimized formula was determined based on the inhibition effect, rheological properties, and cost. The results indicate that crumb rubber-modified asphalts release more fume components with an increment in the temperature and crumb rubber content. Desulfurized rubber reduces the release of H2S and NO. Benzene compounds, including paraxylene, toluene, and benzene, are the most released pollutants that harm human health, especially DS CRA 20% and CRA 50%. Kaolin powder and expanded graphite have a sufficient pore structure and volume, the addition of which reduces the release of pollutants while possibly promoting the release of NO and H2S. Their addition also has a significant control effect on the release of particulate matter at 170 °C and 185 °C. With the consideration of emissions, rheological properties, and cost, CRA 40%-EG2%-KL2% was determined as the optimization formula. This research is helpful to the application of crumb rubber-modified asphalt in road construction and maintenance.

Extensive investigation of seasonal and spatial fluctuations of BTEX in an industrial city with a health risk assessment

There are many pollutants in the air that can be harmful to human health. Their impact varies based on factors such as the kind of pollutant, duration of exposure, and concentration levels. Volatile organic compounds are particularly significant carcinogens among the various pollutants present in the air. Consequently, people who are exposed to these harmful airborne pollutants suffer permanent consequences. This study examines the properties of BTEX compounds—benzene, toluene, ethylbenzene, and xylene—as well as their sources and risk assessments throughout a one-year period from March 21, 2019, to March 20, 2020, in Karaj, Iran’s largest industrialized city. First, utilizing a geographical information system that covered the entire city, 17 locations within Karaj were chosen for this purpose. Then, samplings were carried out in the spring, summer, autumn, and winter months with the NIOSH 1501 method. During the research period, 68 samples of BTEX compounds were collected. The adsorption of these contaminants on the activated carbon adsorbents was performed using an environmental sampling pump with a flow rate of 0.2 L/min for 1 h. The samples were subsequently prepared using a carbon disulfide solution and injected into a GC-FID for analysis. In this research, the average annual concentration of BTEX compounds in the air of Karaj city was obtained at 33.01 µg/m3. Autumn and spring had the highest and lowest average concentrations of BTEX compounds, respectively. In addition, sites 5 and 8 had the highest average annual concentrations of these pollutants. The sourcing conducted in this study showed that transportation and fuel consumption, as well as industries, were the primary sources of pollution in the city. In addition, the excess lifetime cancer risk was higher than the guideline value in some sites and lower in others. Furthermore, the Hazard Quotients were lower than 1, but in general, the citizens of Karaj were at serious risk from exposure to this group of pollutants.

The impact of climatic conditions on the carcinogenic and non-carcinogenic risk of BTEX compounds: A systematic review and meta-analysis

Climatic conditions are one of the most important factors affecting the risk level associated with exposure to benzene, toluene, ethylbenzene, and xylene (BTEX) compounds. This systematic review and meta-analysis study aimed to investigate the impact of climatic conditions on carcinogenic and non-carcinogenic risk value changes during exposure to BTEX compounds. Five electronic bibliographic databases (Scopus, PubMed, Medline, Embase, and Web of Science) were systematically searched. The search algorithm consisted of three sets of keywords and their possible combinations. For different climatic conditions, the overall mean and 95 % confidence interval (CI) of the effect size related to the carcinogenic and non-carcinogenic risk of BTEX were calculated using a random effect model. 26 articles passed the inclusion/exclusion criteria and were included in this review. The highest values of the hazard quotient (HQ) for benzene, toluene, ethylbenzene, and xylene were in the summer season (53.3 %, 47.1 %, 73.3 %, 68.8 % of the studies) and in the winter season (33.3 %, 47.1 %, 20 %, and 25 % of the studies), respectively. Additionally, the highest values of carcinogenic risk (CR) for benzene and ethylbenzene were revealed in the summer season (50 % and 75 % of the studies) and in the winter season (33.3 % and 25 % of the studies), respectively. Based on the results of the meta-analysis also, risk values related to occupational and environmental exposures in summer were often higher than those in winter. These results can be used by policymaking to focus on decreasing exposure to BTEX, particularly in climatic conditions with higher hazards.

Volatile organic compounds in exhaled breath of newborns: a pilot study.

To assess volatile organic compounds (VOCs) in breath samples collected non-invasively from preterm and full-term infants. This was a pilot study included preterm and full-term infants who were not intubated or suspected or diagnosed with metabolic or gastrointestinal disorders. The samples were analyzed for VOCs using a selected-ion flow-tube mass spectrometer. Twenty infants were included; ten preterm and ten full-term infants. Twenty-two VOCs were detected and measurable in all samples. There was a significant difference between preterm and full-term infants for the 2-propanol, acetaldehyde, acetone, acetonitrile, benzene, ethanol, isoprene, pentane, 3-methylhexane, 2-nonene, ethane, triethylamine, and trimethylamine compounds. It is feasible to measure VOCs in breath samples of preterm and full-term non-intubated infants. Full-term infants express different concentrations than preterm infants. Further studies are needed to examine the utility and reproducibility of measuring VOCs to identify neonatal diseases and predict outcomes.

Can Graph Machines Accurately Estimate 13C NMR Chemical Shifts of Benzenic Compounds?

In the organic laboratory, the 13C nuclear magnetic resonance (NMR) spectrum of a newly synthesized compound remains an essential step in elucidating its structure. For the chemist, the interpretation of such a spectrum, which is a set of chemical-shift values, is made easier if he/she has a tool capable of predicting with sufficient accuracy the carbon-shift values from the structure he/she intends to prepare. As there are few open-source methods for accurately estimating this property, we applied our graph-machine approach to build models capable of predicting the chemical shifts of carbons. For this study, we focused on benzene compounds, building an optimized model derived from training a database of 10,577 chemical shifts originating from 2026 structures that contain up to ten types of non-carbon atoms, namely H, O, N, S, P, Si, and halogens. It provides a training root-mean-squared relative error (RMSRE) of 0.5%, i.e., a root-mean-squared error (RMSE) of 0.6 ppm, and a mean absolute error (MAE) of 0.4 ppm for estimating the chemical shifts of the 10k carbons. The predictive capability of the graph-machine model is also compared with that of three commercial packages on a dataset of 171 original benzenic structures (1012 chemical shifts). The graph-machine model proves to be very efficient in predicting chemical shifts, with an RMSE of 0.9 ppm, and compares favorably with the RMSEs of 3.4, 1.8, and 1.9 ppm computed with the ChemDraw v. 23.1.1.3, ACD v. 11.01, and MestReNova v. 15.0.1-35756 packages respectively. Finally, a Docker-based tool is proposed to predict the carbon chemical shifts of benzenic compounds solely from their SMILES codes.

Association Between Benzene and Other Volatile Organic Compounds Exposure and Diabetes Mellitus Among Korean Adults: Findings from the Nationwide Biomonitoring Data

Association Between Benzene and Other Volatile Organic Compounds Exposure and Diabetes Mellitus Among Korean Adults: Findings from the Nationwide Biomonitoring Data

Theoretical Study on the Pyrolysis Mechanism of the Lignin Dimer Model Compound Catalyzed by Alkaline Earth Metal Ions Ca2+ and Mg2+

It is essential to investigate the influence of alkaline earth metals on the pyrolysis mechanism and resulting products of lignin to enhance the efficient thermochemical conversion and utilization of lignin or biomass. In this study, the density functional theory method was used to simulate the pyrolytic reaction pathways of a β-O-4 type lignin dimer model compound (1-methoxy-2-(4-methoxyphenethoxy)benzene, mc) affected by alkaline earth metal ions Ca2+ and Mg2+. The computational findings suggest that Ca2+ and Mg2+ tend to combine with the oxygen atom at the Cβ position and the oxygen atom on the methoxy group of the lignin dimer model compound, forming stable complexes that modify the bond lengths of the Cα–Cβ and Cβ–O bonds and affect their pyrolysis energy barriers. During the catalytic pyrolysis process, the presence of Ca2+ and Mg2+ can promote the concerted decomposition reaction, leading to increased production of products like 1-methoxy-4-vinylbenzene, 2-methoxyphenol and catechol. Meanwhile, they can suppress homolytic cleavage reactions of the Cβ–O and Cα–Cβ bonds, thereby hindering the formation of other products such as 1-ethyl-4-methoxybenzene and 2-hydroxybenzaldehyde.

A comprehensive study on the spatial and temporal variation of BTEX and asbestos in the northwest of Iran: Human risk assessment

Substances like asbestos and other air pollutants, such as BTEX (benzene, toluene, ethylbenzene, and xylene), are hazardous compounds due to their adverse effects on human health. This study aims to investigate the levels, seasonal variations, spatial distribution, potential sources, and associated health risks associated with BTEX compounds and asbestos fibers in the ambient air of Tabriz. Air samples were taken at 16 different locations during the 2020–2021 period. Glass containers with charcoal were used for sample collection, and the BTEX content was determined using the GC-FID method. Phase-contrast microscopy (PCM) analysis was conducted with a low-volume peripheral pump for asbestos fiber sampling. The results showed that the average concentration of ∑BTEX was 37.94 and 27.98 μg/m3 in autumn and spring, respectively. The same parameter was 2.26 and 1.68 f/L for asbestos in the autumn and winter, respectively. The contribution of BTEX to ozone formation potential (OFP) in the research area showed that xylene and toluene were the major contributors to ozone production in different seasons. The risk of exposure to benzene compounds was 24 × 10−4 in children and 55.9 × 10−4 in adults, while the risk of exposure to ethylbenzene was 3.78 × 10−4 in children and 3.25 × 10−4 in adults. The estimated lifetime cancer risk was found to be the highest for benzene, followed by ethylbenzene. The estimated cancer risk for benzene and ethylbenzene exceeded the threshold values set by EPA, which signals a significant carcinogenic risk due to exposure to these substances in the ambient air of Tabriz. According to the EPA guidelines, the low carcinogenicity risk levels are between 10−4 and 10−6. According to the findings for the exposure to asbestos fibers, the maximum values of excess cancer risk (ECR) and estimated lifetime cancer risk (ELCR) were observed in the 16–30 age range across all locations, suggesting increased exposure to asbestos fibers compared to other age groups.

Chlorination mechanism of benzene series in aqueous system under the combined action of Cl- and multiple free radicals

In this study, non-targeted analysis revealed that the Fe2+/perodisulfate/Cl- system degraded aniline (AN) and nitrobenzene (NB), yielding 7 types and 4 types of aromatic chlorides, respectively. In order to explore their chlorination mechanism and the influence of different functional groups, various reactions (radical adduct formation (RAF), hydrogen atom abstraction (HAA) and single electron transfer (SET)) of benzene series with various functional group with sulfate radical (SO4·-), hydroxyl radical (·OH), chlorine radical (·Cl) and dichloride anion radicals (Cl2·-) were explored by Gibbs free energy (ΔG), and the subsequent reactions of SET and HAA products (organic free radical) were innovatively explored by ΔG. This study revealed that the reaction between benzene compounds containing electron-donating groups and ·Cl was dominated by HAA rather than RAF; the reaction between benzene compounds containing electron-withdrawing groups and ·Cl was dominated by RAF. Aromatic compounds containing electron-donating groups can undergo SET reaction and generate aromatic chlorides in the presence of O2 and Cl-. Combined with the product analysis, it was found that the HAA reaction of aromatic compounds will lead to the obvious formation of biphenyl compounds and aromatic chlorides in the presence of Cl-. Compared with the conditions of RAF of ·Cl and chlorination of SET products, the chlorination reaction between HAA products and Cl- is ubiquitous, which is more likely to be the key to the formation of aromatic chlorides in mixed systems. This study provides a theoretical basis for further study on the formation risk of chlorinated products in advanced oxidation process.

Alternative Reactions to Friedel-crafts Acylation on Highly Activated Substrates

Abstract: Friedel-Crafts acylation (FCAcyl) is the most widespread method used to prepare aryl ketones and aldehydes. However, depending on the type of group attached to the benzene, their derivatives influence the electronic characteristics and structural orientations of the compounds during acylation; thus, the groups are very important for the success of the reaction. The existence of strong electron-donating groups, such as polyhydroxy/ polyalkoxyphenols and anilines on the aromatic ring, makes this reaction difficult. To overcome these problems and with the aim of obtaining aromatic ketones from benzene compounds, appropriate methodologies were described. Therefore, this review consists of showing the importance and applicability of the Houben- Hoesch and Sugasawa reactions as alternatives for the Friedel-Crafts acylation of polyhydroxy/ polyalkoxyphenols and anilines, respectively. The main advances used in the original methodologies were also described. The use of these reactions as an alternative to the renowned Friedel-Crafts acylation reactions should be taken into consideration as an important synthetic tool because there is the possibility of reducing steps, with consequent improvement of yield, in addition to optimizing reaction performance.

The product of hydrogenation of a model mixture of alkyl-substituted C7—C12 benzene compounds as a new liquid organic carrier of hydrogen

The product of hydrogenation of a model mixture of alkyl-substituted C7—C12 benzene compounds as a new liquid organic carrier of hydrogen

VOC data-driven evaluation of vehicle cabin odor: from ANN to CNN-BiLSTM.

Emissions of volatile organic compounds (VOCs) in vehicles represent a significant problem, causing unpleasant odors. To mitigate VOCs and odors in vehicles, it is critical to choose interior parts with low odor and VOC emissions. However, prevailing odor evaluation methods are subjective, costly, and potentially harmful to the health of evaluators. In this study, we analyzed 139 automotive interior parts and 92 vehicles, establishing a cost-effective, data-driven method for odor evaluation. The contents of benzene, toluene, ethylbenzene, xylene, styrene, formaldehyde, acetaldehyde, acrolein, and total volatile organic compounds (TVOC) were detected by thermal desorption gas chromatography-mass spectrometry (TD-GC/MS) and high-performance liquid chromatography with an ultraviolet detector (HPLC-UV). Professional odor evaluators assessed the odors, identifying intensity levels from 2.0 to 4.5 in interior parts and 2.5 to 3.5 in whole vehicles. Leveraging this data, we applied four supervised learning algorithms to develop predictive models for the odor intensity of both interior parts and entire vehicles. During model training, we implemented early stopping techniques for the artificial neural network (ANN) and convolutional neural network-bidirectional long short-term memory (CNN-BiLSTM) models, while optimizing the support vector machine (SVM) and extreme gradient boosting (XGBoost) models using the GridSearch algorithm. The evaluation results reveal that the CNN-BiLSTM model performs the best, achieving an average accuracy of 89% for unknown samples within an odor intensity level of 0.5. The root mean square error (RMSE) is 0.24, and the mean absolute error (MAE) is 0.08. The model also underwent a sevenfold cross-validation, achieving an accuracy of 83.43%. Additionally, we employed SHapley Additive exPlanations (SHAP) for the interpretative analysis of the model, which confirmed the consistency of each VOC's odor contribution with human olfactory rules. By predicting odors based on VOCs through supervised learning, this study reduces the costs and enhances the efficiency and applicability of odor assessment across various vehicle interiors.

The promoting and inhibitory mechanism of interaction between waste tires and Spirulina on their co-pyrolysis

Energy utilization of biomass and waste is an important thrust for carbon emission reduction. Co-pyrolysis is conductive to efficiently converting algae and waste tires, due to their complementary pyrolysis characteristics. However, the influence of the interaction between algae and waste tires on co-pyrolysis behavior is still controversial, due to the internal mechanism of interaction is unclear. Therefore, in this study, mechanism experiments and theoretical calculations were used to comprehensively investigate the interaction mechanism between Spirulina (SP) and waste tires (WT). The co-pyrolysis of SP and WT can be divided into two main steps: low-temperature SP decomposition and high-temperature WT decomposition. The activation energies of WT and mixture increase with the conversion rate, while those of SP change little at low conversion rates (<60 %). The pyrolysis activation energies of mixture are lower than the theoretical values, as the blending ratio of SP below 50 %. The interaction between SP and WT has both promoting and inhibiting effects on the pyrolysis of mixture. The attack of free radicals from SP pyrolysis and ash in WT promotes the pyrolysis of mixture, but the low-temperature polymerization reactions and high-temperature aromatization reactions inhibit the release of pyrolysis products. The formation of benzene compound is promoted due to the attack of free radicals and the polymerization between SP and WT.

Exposure to benzene, toluene, ethylbenzene, and xylene (BTEX) at Nigeria's petrol stations: a review of current status, challenges and future directions.

In Nigeria, because of increasing population, urbanization, industrialization, and auto-mobilization, petrol is the most everyday non-edible commodity, and it is the leading petroleum product traded at the proliferating Nigeria's petrol stations (NPSs). However, because of inadequate occupational health and safety (OHS) regulatory measures, working at NPSs exposes petrol station workers (PSWs) to a large amount of hazardous benzene, toluene, ethylbenzene, and xylene (BTEX) compounds. Studies on BTEX exposures among Nigerian PSWs are scarce. Thus, constraints in quantifying the health risks of BTEX limit stakeholders' ability to design practical risk assessment and risk control strategies. This paper reviews studies on the OHS of Nigerian PSWs at the NPSs. Although knowledge, attitude, and practices on OHS in NPSs vary from one Nigeria's study setting to another, generally, safety practices, awareness about hazards and personal protective equipment (PPE), and the use of PPE among PSWs fell below expectations. Additionally, air quality at NPSs was poor, with a high content of BTEX and levels of carbon monoxide, hydrogen sulfide, particulate matter, and formaldehyde higher than the World Health Organization guideline limits. Currently, regulatory bodies' effectiveness and accountability in safeguarding OHS at NPSs leave much to be desired. Understanding the OHS of NPSs would inform future initiatives, policies, and regulations that would promote the health and safety of workers at NPSs. However, further studies need to be conducted to describe the vulnerability of PSWs and other Nigerians who are occupationally exposed to BTEX pollution. More importantly, controlling air pollution from hazardous air pollutants like BTEX is an essential component of OHS and integral to attaining the Sustainable Development Goals (SDG) 3, 7, and 11.

The impact of ozone treatment on the removal effectiveness of various refractory compounds in wastewater from petroleum refineries

Large volumes of wastewater are generated during petroleum refining processes. Petroleum refinery wastewater (PRW) can contain highly toxic compounds that can harm the environment. These toxic compounds can be a challenge in biological treatment technologies due to the effects of these compounds on microorganisms. These challenges can be overcome by using ozone (O3) as a standalone or as a pretreatment to the biological treatment. Ozone was used in this study to degrade the organic pollutants in the heavily contaminated PRW from a refinery in Mpumalanga province of South Africa. The objective was achieved by treating the raw PRW using ozone at different ozone treatment times (15, 30, 45, and 60 min) at a fixed ozone concentration of 3.53 mg/dm3. The ozone treatment was carried out in a 2-liter custom-designed plexiglass cylindrical reactor. Ozone was generated from an Eco-Lab-24 corona discharge ozone generator using clean, dry air from the Afrox air cylinder as feed. The chemical oxygen demand, gas chromatograph characterization, and pH analysis were performed on the pretreated and post-treated PRW samples to ascertain the impact of the ozone treatment. The ozone treatment was effective in reducing the benzene, toluene, ethylbenzene, and xylenes (BTEX) compounds in the PRW. The 60-min ozone treatment of different BTEX pollutants in the PRW resulted in the following percentage reduction: benzene 95%, toluene 77%, m + p-xylene 70%, ethylbenzene 69%, and o-xylene 65%. This study has shown the success of using ozone in reducing the toxic BTEX compounds in a heavily contaminated PRW.

Conversion of lignin-derived ketonic intermediate to biofuel products: Syngas-assisted vs. Conventional hydrotreating

A new strategy for the transformation of an intermediate of the lignin conversion process, namely cyclohexanone, to fuel-grade products is assessed in this study. In this regard, the conventional hydrodeoxygenation process (with pure hydrogen) was compared to an innovative one with a simulated lignin-derived syngas stream in a wide range of reaction conditions (300–400 °C, 1–15 bar, and small-to-large feed-to-catalyst ratios) and over commercial molybdenum-based (nickle‑molybdenum (NiMo) and cobalt‑molybdenum(CoMo)) catalysts. Cyclohexanone conversion, product distribution, deoxygenation efficacy, and heating value were compared in each case. Cyclohexanone was transformed into cyclohexane, cyclohexene, benzene, cresols, phenol, toluene, and bi-cyclic compounds, which are beneficial in jet-fuel processing. Increasing the reaction temperature and pressure intensified the conversion of cyclohexanone (up to 87.8% conversion at 400 °C and 15 bar over both NiMo and CoMo catalysts), whereas increasing the feed-to-catalyst ratio reduced it. Operating conditions and the reducing gas (pure hydrogen or syngas) had major impacts on the conversion of cyclohexanone, deoxygenation efficiency, product distribution, and the heating value of the final product blend. The results of this study claim that cyclohexanone conversion to fuel-grade hydrocarbons (up to 97.61% over NiMo and 74.71% over CoMo catalysts) is a beneficial route and the conventional hydrodeoxygenation process can be replaced with the syngas-assisted one with a small change in production capacity, still large positive impact on the sustainability and environmental footprints of lignin conversion to biofuels.

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.