Aromatic Hydrocarbon Compounds Research Articles

Development of an effective QSAR-based hazard threshold prediction model for the ecological risk assessment of aromatic hydrocarbon compounds.

The insufficient hazard thresholds of specific individual aromatic hydrocarbon compounds (AHCs) with diverse structures limit their ecological risk assessment. Thus, herein, quantitative structure-activity relationship (QSAR) models for estimating the hazard threshold of AHCs were developed based on the hazardous concentration for 5% of species (HC5) determined using the optimal species sensitivity distribution models and on the molecular descriptors calculated via the PADEL software and ORCA software. Results revealed that the optimal QSAR model, which involved eight descriptors, namely, Zagreb, GATS2m, VR3_Dzs, AATSC2s, GATS2c, ATSC2i, ω, and Vm, displayed excellent performance, as reflected by an optimal goodness of fit (R2adj = 0.918), robustness (Q2LOO = 0.869), and external prediction ability (Q2F1 = 0.760, Q2F2 = 0.782, and Q2F3 = 0.774). The hazard thresholds estimated using the optimal QSAR model were approximately close to the published water quality criteria developed by different countries and regions. The quantitative structure-toxicity relationship demonstrated that the molecular descriptors associated with electrophilicity and topological and electrotopological properties were important factors that affected the risks of AHCs. A new and reliable approach to estimate the hazard threshold of ecological risk assessment for various aromatic hydrocarbon pollutants was provided in this study, which can be widely popularised to similar contaminants with diverse structures.

Three strategy rules of filamentous fungi in hydrocarbon remediation: an overview.

Remediation of hydrocarbon contaminations requires much attention nowadays since it causes detrimental effects on land and even worse impacts on aquatic environments. Tools of bioremediation especially filamentous fungi permissible for cleaning up as much as conceivable, at least they turn into non-toxic residues with less consumed periods. Inorganic chemicals, CO2, H2O, and cell biomass are produced as a result of the breakdown and mineralization of petroleum hydrocarbon pollutants. This paper presents a detailed overview of three strategic rules of filamentous fungi in remediating the various aliphatic, and aromatic hydrocarbon compounds: utilizing carbons from hydrocarbons as sole energy, Co-metabolism manners (Enzymatic and Non-enzymatic theories), and Biosorption approaches. Upliftment in the degradation rate of complex hydrocarbon by the Filamentous Fungi in consortia scenario we can say, "Fungal Talk", which includes a variety of cellular mechanisms, including biosurfactant production, biomineralization, and precipitation, etc., This review not only displays its efficiency but showcases the field applications - cost-effective, reliable, eco-friendly, easy to culture as biomass, applicable in both land and any water bodies in operational environment cleanups. Nevertheless, the potentiality of fungi-human interaction has not been fully understood, henceforth further studies are highly endorsed with spore pathogenicity of the fungal species capable of high remediation rate, and the gene knockout study, if the specific peptides cause toxicity to any living matters via Genomics and Proteomics approaches, before application of any in situ or ex situ environments.

Investigation of Asphaltene Precipitation and Reservoir Damage during CO2 Flooding in High-Pressure, High-Temperature Sandstone Oil Reservoirs

Summary Asphaltenes are heavy aromatic hydrocarbon compounds contained in reservoir fluids and may precipitate when the reservoir pressure is reduced by production or when gas is injected into the reservoir, and then further deposit on pore-throat surfaces causing reservoir damage. At present, the research on asphaltene precipitation and reservoir damage is carried out in conventional reservoirs, and the influence of CO2 injection under high-pressure, high-temperature (HPHT) conditions has not yet been clearly understood. In this work, we combined perturbed-chain statistical association fluid theory (PC-SAFT) calculation, experiments, phase-state simulation, and numerical simulation to predict the asphaltene precipitation with different pressures, temperatures, and amounts of injected gas and to clarify the influence on reservoir permeability and oil production when using CO2 injection. The results show that the precipitation of asphaltenes in the process of CO2 injection is the desorption of colloid-asphaltene inclusions caused by gas molecules and then the mutual polymerization process between dispersed asphaltene molecules. CO2 injection will increase the amount of precipitation and move the precipitation curve to the right side. The degree of permeability reduction caused by the deposition of asphaltenes in the core is 12.87–37.54%; the deposition of asphaltenes in the reservoir is mainly around the injection/production wells and along the injected gas profile. Considering asphaltenes, the oil recovery degree is reduced by 1.5%, and the injection rate is reduced by 17%. The reservoir pressure, temperature, and physical properties have a strong correlation with the degree of reservoir damage, while the initial asphaltene content has a low correlation. This work will be of great interest to operators seeking to enhance oil recovery by CO2 injection in deep reservoirs.

Activated carbon and their nanocomposites derived from vegetable and fruit residues for water treatment

Water pollution remains a pressing environmental issue, with diverse pollutants such as heavy metals, pharmaceuticals, dyes, and aromatic hydrocarbon compounds posing a significant threat to clean water access. Historically, biomass-derived activated carbons (ACs) have served as effective adsorbents for water treatment, owing to their inherent porosity and expansive surface area. Nanocomposites have emerged as a means to enhance the absorption properties of ACs, surpassing conventional AC performance. Biomass-based activated carbon nanocomposites (ACNCs) hold promise due to their high surface area and cost-effectiveness. This review explores recent advancements in biomass-based ACNCs, emphasizing their remarkable adsorption efficiencies and paving the way for future research in developing efficient and affordable ACNCs. Leveraging real-time communication for ACNC applications presents a viable approach to addressing cost concerns.

Temporal and spatial distribution of polycyclic aromatic hydrocarbons (PAHs) in the Danube River in Hungary

The Danube is a significant transboundary river on a global scale, with several tributaries. The effluents from industrial operations and wastewater treatment plants have an impact on the river's aquatic ecosystem. These discharges provide a significant threat to aquatic life by deteriorating the quality of water and sediment. Hence, a total of 16 Polycyclic Aromatic Hydrocarbons (PAHs) compounds were analyzed at six locations along the river, covering a period of 12 months. The objective was to explore the temporal and spatial fluctuations of these chemicals in both water and sediment. The study revealed a significant fluctuation in the concentration of PAHs in water throughout the year, with levels ranging from 224.8 ng/L during the summer to 365.8 ng/L during the winter. Similarly, the concentration of PAHs in sediment samples varied from 316.7 ng/g in dry weight during the summer to 422.9 ng/g in dry weight during the winter. According to the Europe Drinking Water Directive, the levels of PAHs exceeded the permitted limit of 100 ng/L, resulting in a 124.8% rise in summer and a 265.8% increase in winter. The results suggest that the potential human-caused sources of PAHs were mostly derived from pyrolytic and pyrogenic processes, with pyrogenic sources being more dominant. Assessment of sediment quality standards (SQGs) showed that the levels of PAHs in sediments were below the Effect Range Low (ERL), except for acenaphthylene (Acy) and fluorene (Fl) concentrations. This suggests that there could be occasional biological consequences. The cumulative Individual Lifetime Cancer Risk (ILCR) exceeds 1/104 for both adults and children in all sites.

Bacterial biodegradation of oil-contaminated soil for pollutant abatement contributing to achieve sustainable development goals: A comprehensive review

Petroleum hydrocarbon-induced environmental degradation has escalated, necessitating immediate remediation due to the ongoing growth of communities and modernization of civilization. Both carbon and energy can be obtained from hydrocarbons of petroleum, which are decomposed by a wide variety of microorganisms found in nature. Many times, remediation of places damaged by oil using biological means is accomplished by using bacteria that have such characteristics. Hence, this review attempt to highlight on the oil contaminated soil, source of oil pollution, the composition of oil, the impact of oil contamination on the living organisms additionally, the destiny of oil in the environment, how bacteria distributed in the soil and the most common degradable bacteria and their role in oil biodegradation with some attention on the impact of their enzymes. Also, considering the mechanism of biodegradation of aliphatic and aromatic oil hydrocarbon compounds, how bacteria taking up oil hydrocarbons and the influence of several elements on the processes of oil biodegradation. Furthermore, it; reducing pollution contributes to achieving sustainable development goals.

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.

Biomonitoring: Developing a Beehive Air Volatiles Profile as an Indicator of Environmental Contamination Using a Sustainable In-Field Technique

The wellbeing of the honey bee colonies and the health of humans are connected in numerous ways. Therefore, ensuring the wellbeing of bees is a crucial component of fostering sustainability and ecological harmony. The colony collapse disorder (CCD) phenomenon was first reported in 2006 when the majority of bee colonies in Europe died out, due to an increase in infections, contamination of hives with agrochemical pesticides, and persistent organic pollutants (POPs). Only 6 years after the emergence of CCD, more than 6.5 million premature deaths were reported, as a consequence of persistent human exposure to air pollution. The insect species such as the honey bee Apis mellifera L. and the air matrix inside the beehive can be used as tools in biomonitoring, instead of traditional monitoring methods. This may have advantages in terms of cost-effective bioindicators of the environmental health status, showing the ability to record spatial and temporal pollutant variations. In this study, we present the sustainable in-field usage of the portable membrane inlet mass spectrometry (MIMS) instrument for an instant and effective determination of the level of environmental pollution by analytical identification of hive atmosphere volatile organic compound (VOC) contaminants, polycyclic aromatic hydrocarbons (PAHs), polychlorinated biphenyls (PCBs), monocyclic aromatic hydrocarbons (BTEX) compounds, and pesticides. The samples were taken from hives located in urbanized and rural regions, highlighting variations in contamination. The MIMS results were benchmarked against a conventional laboratory sampling technique, such as GC-MS.

Evaluation of polycyclic aromatic hydrocarbon contents in marine products in South Korea and risk assessment using the total diet study

AbstractThis study investigated levels of eight polycyclic aromatic hydrocarbons (PAH8) compounds in both raw and processed marine products in South Korea. Katsuobushi exhibited the highest concentration of benzo[a]pyrene, at 14.22 µg/kg, exceeding the European Commission's regulation level of 5.0 µg/kg. The total PAH8 concentration in katsuobushi was 220.5 µg/kg. Among the product categories, shellfish had the highest detection rate (70%), followed by fish (19%) and crustacea (8%), with chrysene being the most prominent PAH8 congener in all marine products. Grilled fish predominantly contained pyrogenic PAHs from combustion byproducts, while shellfish primarily contained petrogenic ones from the aquatic environment. Grilling, smoking, and drying processes significantly contributed to the formation of PAH8 in these food products. Based on the results of a risk assessment using a margin of exposure approach through a total diet study, exposure to PAH8 from marine products is considered to pose low concern to the South Korean population.

The Effect of the RADEC Model on Conceptual Understanding of Polycyclic Aromatic Hydrocarbons (PAHs) Topic

This study was conducted to analyze the conceptual understanding of students and their struggle on Polycyclic Aromatic Hydrocarbons (PAHs) compounds topic through the implementation of the RADEC Model. Respondents consisted of 37 students from Chemistry Education Department and 33 students from the Chemistry Department at a university in Bandung, Indonesia. This study is an experimental study with a pre-experimental type. Data on conceptual understanding were obtained through pre-tests and post-tests, while data on students’ difficulties were obtained through survey. The data were analyzed using SPSS 24. It was found that there was an increase in the conceptual understanding of the students of Chemistry Education and Chemistry Department in the medium category with n-gain values of 0.33 and 0.38, respectively. The results of inferential analysis through the Wilcoxon Test with Asymp. Sig. (2-tailed) were <0.05 for the two groups of students indicating differences in the pre-test and post-test results with a higher average post-test score. Friedel-Crafts acylation is a concept that is difficult to understand by students from the Chemistry Education Department and the Chemistry Department with the same percentage of 33%. Chemistry Department students also have difficulty understanding the electrophilic substitution concept with a percentage of 33%. As a practical implication, this study successfully showed the effective implementation of the RADEC model, serving as an innovative and beneficial learning approach. The model offered substantial support to students in grasping complex topic such as PAHs compounds.

Improved heterocyclic aromatic hydrocarbon compound adsorption using functionalised rice husk biochar

Carbazole (CBZ) is a hazardous heterocyclic aromatic hydrocarbon (HAH) that pollutes water bodies, and the treatment remains a challenge due to its high persistence in the environment. This study chemically modified rice husk biochar (RHB) with starch derivative (DS) to develop an effective adsorbent. Thus, functionalised RHB with starch derivative (RHBDS) was synthesised to remove CBZ from synthetic wastewater. Based on a Box-Behnken design, the DS functionalisation optimisation was successfully performed. The parameters, including RHB mass of (5–10) g, DS concentration of (1–5)% w/v, and sonication period of (1–5) min, were analysed using Design Expert. These parameters were then utilised to investigate the optimal conditions (removal rate response and adsorption capacity) for the adsorbent. The removal rate and the adsorption capacity ranged from 83.85 to 98.94 % and 335.41 to 395.76 mg/g, respectively. Consequently, the RHB mass of 6.50 g, DS concentration of 1 % w/v, and sonication period of 5 min within the experimental domain exhibited the best conditions with desirability of 1.0. The 92.67 % removal rate and adsorption capacity of 370.59 mg/g were also obtained under optimal conditions. Compared to RHB, RHBDS demonstrated four times the adsorption capacity for the CBZ removal from synthetic water, which were 23.03 mg/g and 98.01 mg/g, respectively. Therefore, the RHBDS compound could be a promising adsorbent in removing CBZ from wastewater.

Understanding of the effect of oxygen on soot formation during non-catalytic partial oxidation process

Non-catalytic partial oxidation (NC-POX) process is a promising technology for hydrogen and syngas production, but the generation of soot hinders its development. In this study, the yields of soot and its precursors under different working conditions are quantified by experiments. When the O2/CH4 ratio is more than 0.6, the soot yield can be controlled below 1.07% from 2.53%. The soot precursor evolution mechanism in NC-POX is analyzed through the quantification of polycyclic aromatic hydrocarbon (PAH) compounds. It is found that hydrogen abstraction vinyl radical addition (HAVA*) and methyl addition cyclization (MAC) are the main growth pathways of PAHs. The concentrations of H2O, CO2, and oxygenated hydrocarbons increase with O2/CH4, which further inhibit the soot generation reactions and reduce the degree of graphitization of soot particles through surface reactions. A soot formation mechanism is proposed. This study provides a quantified reference for soot modeling and the elimination of soot in industry.

Analysis of Polycyclic Aromatic Hydrocarbons Using Magnetic Three-Dimensional Graphene Solid-Phase Extraction Coupled with Gas Chromatography–Mass Spectrometry

In this study, a composite material consisting of three-dimensional graphene aerogel and iron oxide nanoparticles (3DG/Fe3O4) was created and utilized for the purpose of magnetic solid-phase extraction (MSPE) of thirteen polycyclic aromatic hydrocarbon (PAH) compounds via gas chromatography–mass spectrometry/selected ion monitoring (GC-MS/SIM) analysis. The synthesized adsorbent underwent a range of characterization techniques, including scanning electron microscopy, vibrating sample magnetometry, Raman spectroscopy, X-ray diffraction, Brunauer–Emmett–Teller, Fourier transform-infrared spectroscopy, and Barrett–Joyner–Halenda techniques, to examine its properties and morphology. The synthesized adsorbent integrates the benefits of superior adsorption capacity from modified graphene oxide (GO) with the magnetic separability of magnetite microparticles, resulting in a high adsorption capacity with easy separation from sample solutions. The efficiency of the proposed method was optimized and modeled using a central composite design (CCD), which considered the primary factors influencing it. The optimal conditions were obtained as the adsorbent dosage of 10 mg, the extraction time of 4 min, and the salt concentration of 3% w/v. The limit of detection for the target PAHs was established to range from 0.016 to 0.2 ng mL−1 in optimal conditions, exhibiting a signal-to-noise ratio of 3. The linear dynamic range spanned from 5 to 100 ng mL−1, with determination coefficients (R2) ranging from 0.9913 to 0.9997. The intra- and inter-day precisions were calculated as relative standard deviations (RSDs) equal to 3.9% and 4.7%, respectively. The proposed method was successfully applied to the determination of PAHs in water samples (tap, river, and rainwater), and recoveries in the range of 71–110% (RSDs < 5.2%, n = 3) were obtained.

Association of urinary arsenic, polycyclic aromatic hydrocarbons, and metals with cancers among the female population in the US

Cancers that primarily affect women in the US include breast, uterine, and cervical cancers. There may be associations between these different types of cancer in women and environmental pollutant exposure. This study aimed to assess seven species of arsenic, six polycyclic aromatic hydrocarbon (PAH) compounds, and fourteen different metal concentrations in urine and their correlation with cancer among women. We conducted a cross-sectional analysis using 2011--2012 to 2015-2016 National Health and Nutrition Examination Survey data (n=4,956) and logistic regression modeling of the complex weighted survey design. Breast cancer was inversely correlated with arsenocholine (3rd quantile), monomethylarsonic acid (4th quantile), manganese (4th quantile), and antimony (3rd, 4th quantiles). Cervical cancer was inversely correlated with 3-hydroxyfluorene (3rd quantile), molybdenum (2nd, 4th quantiles), antimony (3rd quantile), tin (4th quantile), and thallium (4th quantile) exposure and positively associated with arsenic acid (3rd quantile), arsenobetaine (2nd, 4th quantiles). Uterine cancer was correlated with 1-hydroxynaphthalene (3rd, 4th quantiles), 2-hydroxynaphthalene (4th quantile), 1-hydroxyphenathrene (2nd, 4th quantiles), 1-hydroxypyrene (3rd quantile), cobalt (2nd, 3rd quantiles) and inversely with mercury (4th quantile). This study determined breast cancer and arsenic and some metal species exposure, indicating an inverse association. Arsenic acid and arsenobetaine exposure showed a positive correlation with cervical cancer. For uterine cancer, the correlations for the PAH compounds and cobalt showed a positive correlation, and the arsenic species and mercury were inversely associated. Further research is required to establish or refute the findings.

Microbial Consortium HJ-SH with Very High Degradation Efficiency of Phenanthrene.

Phenanthrene (PHE) is one of the model compounds of polycyclic aromatic hydrocarbons (PAHs). In this study, a natural PHE-degrading microbial consortium, named HJ-SH, with very high degradation efficiency was isolated from soil exposed to long-term PHE contamination. The results of GC analysis showed that the consortium HJ-SH degraded 98% of 100 mg/L PHE in 3 days and 93% of 1000 mg/L PHE in 5 days, an efficiency higher than that of any other natural consortia, and even most of the engineered strains and consortia reported so far. Seven dominating strains were isolated from the microbial consortium HJ-SH, named SH-1 to SH-7, which were identified according to morphological observation and 16S rDNA sequencing as Pseudomonas sp., Stenotrophomonas sp., Delftia sp., Pseudomonas sp., Brevundimonas sp., Curtobacterium sp., and Microbacterium sp., respectively. Among all the seven single strains, SH-4 showed the strongest PHE degradation ability, and had the biggest degradation contribution. However, it is very interesting that the microbial consortium can hold its high degradation ability only with the co-existence of all these seven single strains. Moreover, HJ-SH exhibited a very high tolerance for PHE, up to 4.5 g/L, and it can degrade some other typical organic pollutants such as biphenyl, anthracene, and n-hexadecane with the degradation ratios of 93%, 92% and 70%, respectively, under 100 mg/L initial concentration in 5 days. Then, we constructed an artificial consortium HJ-7 consisting of the seven single strains, SH-1 to SH-7. After comparing the degradation ratios, cell growth, and relative degradation rates, it was concluded that the artificial consortium HJ-7 with easier reproducibility, better application stability, and larger room for modification can largely replace the natural consortium HJ-SH. In conclusion, this research provided novel tools and new insights for the bioremediation of PHE and other typical organic pollutants using microbial consortia.

Characterization, ratio analysis, and carcinogenic risk assessment of polycyclic aromatic hydrocarbon compounds bounded PM10 in a southwest of Iran

Background/objectivesA group of environmental carcinogens are polycyclic aromatic hydrocarbons (PAHs) that are formed during the incomplete combustion of organic materials. The aims of this study was evaluated the Characterization, ratio analysis, and carcinogenic risk assessment of polycyclic aromatic hydrocarbon compounds bounded PM10 in a southwest of Iran. MethodsIn this descriptive-cross-sectional study, was conducted in every 4 seasons. In each region, 20 air samples and a total of 40 samples were collected by the OMNI device in two regions. ResultsBased on result of this study in the cold season the average concentration total of PAHs was higher than in the hot season. Anthracene and fluorine with 4.70 and 4.25 ng/m3 in the cold season and naphthalene and anthracene with 4.07 and 3.48 ng/m3 in the warm season were the highest mean concentration among other organic compounds. The results of diagnostic ratios also showed that the main source PAHs of in the air of Shushtar city is fossil fuel and the use of gasoline cars. ConclusionAccording to the results the mean amount of PAHs in the cold season is higher than in the hot season, and the effects of temperature on it can aggravate these pollutants. Considering that PAHs are mainly produced as a result of the use of fossil fuels and transportation, it is necessary to pay more attention to these pollutants and control the sources of their emission. It is also necessary to create a culture in society in order to increase the use of public transportation.

Distinct laccase expression and activity profiles of Trametes versicolor facilitate degradation of benzo[a]pyrene.

A Trametes versicolor isolate from the Changbai Mountain showed promising activity in degrading benzo[a]pyrene (BaP), which is a high molecular weight (HMW) polycyclic aromatic hydrocarbon (PAH) compound. It was hypothesized that the T. versicolor isolate encode BaP-degrading enzymes, among which laccase is mostly sought after due to significant commercial potential. Genome of the T. versicolor isolate was sequenced and assembled, and seven laccase homologues were identified (TvLac1-7) as candidate genes potentially contributing to BaP degradation. In order to further identify the BaP responsive laccases, time-course transcriptomic and proteomic analyses were conducted in parallel on the T. versicolor isolate upon BaP treatment. Homologous laccases showed distinct expression patterns. Most strikingly, TvLac5 was rapidly induced in the secreted proteomes (secretomes), while TvLac2 was repressed. Recombinant laccase expression and biochemical characterization further showed corresponding enzymatic activity profiles, where TvLac5 was 21-fold more effective in BaP degradation compared to TvLac2. Moreover, TvLac5 also showed 3.6-fold higher BaP degrading activity compared to a commercial laccase product of T. versicolor origin. Therefore, TvLac5 was concluded to be a BaP-responsive enzyme from T. versicolor showing effective BaP degradation activity.

Novel strategy to produce polyaromatic compounds at low temperature for the production of secondary chars

The production of polyaromatic compounds during biomass thermochemical processing at temperatures over 700 °C from the secondary reactions pyrolysis vapors is a well study phenomena. These compounds are sometimes used to produce carbonaceous materials (such as carbon black, carbon nanotubes). In the case of gasification these polyaromatic compounds form tars and are a major source of problems for the operation of these reactors. In this paper we explore the use of acid impregnation, particularly using phosphoric acid, to reduce the temperature at which small polyaromatic rings are formed and released from the biomass. The acid treatment of biomass was found to increase the yield of biochar (from 17 wt% to 40 wt%) and to be an excellent source of polyaromatic compounds (close to 15 wt% on biomass dry basis). In this manuscript we explored the use of the small polyaromatic ring systems produced from the carbonization of acid-pretreated biomass as precursors for the synthesis of secondary carbons. A two-step pyrolysis process was conducted on acid-treated biomass, revealing that the volatiles produced in the first stage were primarily derived from the dehydration of anhydrosugars. In contrast, the volatiles produced in the second stage were found to be primarily composed of aromatic compounds similar to those produced in gasification processes, with low to no oxygen content. In this research, we have introduced an innovative strategy to maximize the benefits of acid-treated biomass pyrolysis by utilizing the low oxygen aromatic hydrocarbons compounds produced as a carbon source for the production of carbon nanostructures (CNS) on biochar-supported nickel catalysts. This methodology allows to produce polyaromatic compounds at very low temperature from lignocellulosic materials. This not only optimizes the utilization of biomass resources but also enhances the yield of high-value products and aligns with the principles of a circular economy.

Aromatic hydrocarbons rich bio-oil production from Miscanthus pyrolysis by coupling torrefaction and MoO3/ZSM-5 dual catalysis process

The valorization of Miscanthus pyrolysis by coupling torrefaction and MoO3/ZSM-5 dual catalysis process was studied to generate the aromatic hydrocarbons rich bio-oil, biochar, and combustible gas. With the optimal conditions of torrefied Miscanthus at 280 °C, MoO3/ZSM-5 catalysis process converted 24.17 % bio-oil, 30.27 % biochar, and 45.56 % gas. The coupled system accessed bio-oil phase deoxygenation by reducing the oxygen-containing compound content to 6.27 %. The aromatic yield reached 91.38 %, with an outstanding benzene, toluene and xylene (BTX) selectivity of 52.24 %. Isolating investigations revealed that torrefaction declined the oxygen content of Miscanthus to 5.24 %, increasing their calorific value and promoting subsequent catalytic pyrolysis through deoxygenation. When only using the ZSM-5 catalyst, the increase in torrefaction temperature enhanced aromatic hydrocarbon compounds conversion in the bio-oil, leading to a boost in their content from 55.01 % to 75.97 %. Correspondingly, MoO3 promoted deoxygenation, decreased the ketone content from 40.4 % to 21.92 %, and inhibited the generation of aldehydes. The combination of MoO3 and ZSM-5 with torrefaction delivered a superimposed effect on yielding aromatic hydrocarbons and BTX, which allowed a promising product upgrading method for obtaining high-quality bio-oil.

Spatial and Temporal variations of Organic Chemical compounds in Ambient Air from Ahmedabad City, Gujarat, India

Organic contaminants linked to atmospheric particulate matter have been a major source of worry across the world since the last decade. The ambient air samples were collected from three sites in Ahmedabad city for spatial and temporal variation using a High-Volume Air Sampler (HVAS) to examine the morphology and elemental composition of fine and ultrafine particles by using a Scanning electron microscope (SEM) and an energy dispersive X-ray system (EDAX) from PM2.5. The Si, C, O, Cl, Na, Al, K, Ca and Mg were found to be quite abundant in the EDAX spectra. Transition elements such as Ti, Zn, Cu, S and Fe were registered, indicating the influence of industry in liberating the abundance of fine and ultrafine particles. In addition, the organic chemical compounds were screened by using GC–MS. A total of 230 organic chemicals were detected, including 187 aliphatic and 43 aromatic chemical compounds at three different locations. Results show that aliphatic and aromatic hydrocarbon compounds were found maximum in the urban area followed by industrial and rural areas.