Aliphatic Research Articles

Defining a core breath profile for healthy, non-human primates

Non-human primates remain the most useful and reliable pre-clinical model for many human diseases. Primate breath profiles have previously distinguished healthy animals from diseased, including non-human primates. Breath collection is relatively non-invasive, so this motivated us to define a healthy baseline breath profile that could be used in studies evaluating disease, therapies, and vaccines in non-human primates. A pilot study, which enrolled 30 healthy macaques, was conducted. Macaque breath molecules were sampled into a Tedlar bag, concentrated onto a thermal desorption tube, then desorbed and analyzed by comprehensive two-dimensional gas chromatography-time of flight mass spectrometry. These breath samples contained 2,017 features, of which 113 molecules were present in all breath samples. The core breathprint was dominated by aliphatic hydrocarbons, aromatic compounds, and carbonyl compounds. The data were internally validated with additional breath samples from a subset of 19 of these non-human primates. A critical core consisting of 23 highly abundant and invariant molecules was identified as a pragmatic breathprint set, useful for future validation studies in healthy primates.

Determination of the Nature of Hydrocarbons in the Barents Sea (Verification of Remote Sensing Data)

Based on remote sensing data on the distribution of oil spills obtained using synthetic aperture radar (SAR) imagery of the Sentinel-1A and Sentinel-1B satellites in 2016–2022 and the results of the analysis of aliphatic hydrocarbons (AHCs) and polycyclic aromatic hydrocarbons (PAHs) in bottom sediments taken in 2019–2022, the nature of oil slicks in various areas of the Barents Sea has been established. It is shown that the distribution of oil slicks in coastal areas is greatly influenced by anthropogenic hydrocarbon inflow (mainly from shipping and fishing), which is confirmed by elevated AHC concentrations in coastal sediments (up to 73 μg/g) and in the composition of Corg (up to 3.6%). In the central and northern regions of the Barents Sea (station 7105, in the coordinates 75.2–75.3 N, 31.5–31.8 E), the grouping of oil slicks is due to natural seepage of oil and gas. This is confirmed by the anomalous concentration of PAHs in the lower horizons of the obtained sediment column, and their composition (the dominance of 2-methylnaphthalene, a marker of their oil genesis). At the same time, the proportion of light homologues in the composition of alkanes increased, which may indicate their formation in the sedimentary sequence.

Chiral inversion induced by aromatic interactions in short peptide assembly

Although hydrophobic interactions provide the main driving force for initial peptide aggregation, their role in regulating suprastructure handedness of higher-order architectures remains largely unknown. We here interrogate the effects of hydrophobic amino acids on handedness at various assembly stages of peptide amphiphiles. Our studies reveal that relative to aliphatic side chains, aromatic side chains set the twisting directions of single β-strands due to their strong steric repulsion to the backbone, and upon packing into multi-stranded β-sheets, the side-chain aromatic interactions between strands form the aromatic ladders with a directional preference. This ordering not only leads to parallel β-sheet arrangements but also induces the chiral flipping over of single β-strands within a β-sheet. In contrast, the lack of orientational hydrophobic interactions in the assembly of aliphatic peptides implies no chiral inversion upon packing into β-sheets. This study opens an avenue to harness peptide aggregates with targeted handedness via aromatic side-chain interactions.

Ni2MnAl Heusler Alloy Nanoparticles for Chemoselective Hydrogenation of Nitro Compounds

AbstractDespite immense interest for years in Heusler alloys as magnetoelastic materials, their application in heterogeneous catalysis has only recently been explored. We report the development of highly active, robust and magnetically separable Ni2MnAl Heusler alloy nanoparticles as a heterogeneous catalyst for hydrogenation of aliphatic and aromatic nitro compounds to the corresponding amines. The easily synthesizable Ni2MnAl nanoparticles are thermally and chemically robust and exhibited excellent chemoselectivity in the hydrogenation of a range of aliphatic and aromatic nitroarenes, including those bearing functional groups sensitive to reduction, such as alkene, bromo, iodo, carbonyl and cyano, yielding the respective functionalized amines in good yields. Moreover, this solid catalyst is magnetically separable from the reaction mixture and could be recycled and reused at least 10 times without any loss in catalytic activity. The mechanism of the Ni2MnAl Heusler alloy nanoparticles catalyzed nitro reduction was studied by various spectroscopy, control experiments and kinetics. Our work opens a new avenue of developing heterogeneous earth‐abundant metal catalysis for economic and environment‐friendly synthesis of fine chemicals owing to straightforward synthesis and tunable composition of Heusler alloy nanoparticles from base‐metal precursors and their diverse structure and properties in conjunction with their thermal and chemical stability, excellent chemoselectivity, magnetic separability and recyclability.

Aliphatic and cyclic hydrocarbons in urban street dust from Riyadh city, Saudi Arabia: Levels, distribution, and sources

Dust particles contain diverse natural and anthropogenic organic compounds and act as local collectors of pollutants, particularly in urban settings. Samples of street dust were collected from various sites in Riyadh city in 2023. These samples were extracted using a dichloromethane–methanol mixture, and the resulting extracts were subjected to analysis through gas chromatography–mass spectrometry (GC–MS). The primary compounds identified included n-alkanes, methyl n-alkanoates (FAMEs), hopanes, steranes, polycyclic aromatic hydrocarbons (PAHs), plasticizers, tobacco miscellanies, and an unresolved complex mixture (UCM). Vegetation detritus constituted the primary natural source of organic compounds, ranging from 7.4 ± 3.5% to 15.0 ± 4.0%, and included fractional n-alkanes and FAMEs. Petroleum-related products from vehicular emissions, oil combustion, and spills were predominant, accounting for 73.3 ± 5.1% to 87.5 ± 4.8%, and included partial n-alkanes, hopanes, steranes, PAHs, and UCMs. Litterings from discarded plastics and tobacco smoking varied from 5.2 ± 1.3% to 12.0 ± 5.3%, and included phthalates, nicotine, and cotinine, as well as recreational drinks (coffee and tea beverages containing caffeine). The occurrence and distribution of natural and anthropogenic extractable organic matter in this arid urban area were influenced by local vegetation and human activities. The prevalence of anthropogenic organic compounds in Riyadh city's street dust depended on the location and type of urban activity, with elevated levels observed in high-traffic and industrial zones. Consequently, further investigations are necessary to understand the potential health effects of anthropogenic organic matter on city residents.

Hydrogen solubility in different chemicals: A modelling approach and review of literature data

Hydrogen (H2) solubility is a crucial parameter for industrial processes. This study utilises various Machine Learning (ML) techniques, including Decision Tree (DT), Multilayer Perceptron (MLP), Random Forest (RF), and Extremely Randomized Trees (ET), to predict H2 solubility across diverse chemical classes, encompassing n-alkanes, aliphatic and aromatic hydrocarbons, alcohols, aldehydes, diols, esters, ethers, ketones, and halides. An extensive database of 4337 samples of H2 solubility in 100 different chemicals was compiled from open literature. Problematic samples were identified through preprocessing. Three input sets were utilised for model development to determine the optimal combination of regressors. It was found that including dimensionless pressure and temperature significantly improved modelling accuracy. Higher accuracy was achieved by employing polynomial extracted features. 76 chemicals trained the model, and 20 tested it, with none overlapping. High accuracy on the test set shows applicability to a diverse chemical range beyond the study's dataset. The study's modelling results indicate RF and ET ensemble methods outperform DT and MLP in accuracy and stability, with ET being the most accurate. This study improves our understanding of H2 solubility in various chemicals, crucial for industrial processes like designing H2-based renewable energy plants. Our study advances ML in predicting chemical solubility by introducing advanced feature extraction and testing models with unseen chemicals. This not only validates our models' predictive capability but also yields deeper insights into H2 solubility. With standardized data preprocessing and a model adept at handling diverse chemicals, we demonstrate a substantial advancement in the field through a meticulous testing methodology.

The impact of transmembrane peptides on lipid bilayer structure and mechanics: A study of the transmembrane domain of the influenza A virus M2 protein

Transmembrane peptides play important roles in many biological processes by interacting with lipid membranes. This study investigates how the transmembrane domain of the influenza A virus M2 protein, M2TM, affects the structure and mechanics of model lipid bilayers. Atomic force microscopy (AFM) imaging revealed small decreases in bilayer thickness with increasing peptide concentrations. AFM-based force spectroscopy experiments complemented by theoretical model analysis demonstrated significant decreases in bilayer's Young's modulus (E) and lateral area compressibility modulus (KA). This suggests that M2TM disrupts the cohesive interactions between neighboring lipid molecules, leading to a decrease in both the bilayer's resistance to indentation (E) and its ability to resist lateral compression/expansion (KA). The large decreases in bilayer elastic parameters (i.e., E and KA) contrast with small changes in bilayer thickness, implying that bilayer mechanics are not solely dictated by bilayer thickness in the presence of transmembrane peptides. The observed significant reduction in bilayer mechanical properties suggests a softening effect on the bilayer, potentially facilitating membrane curvature generation, a crucial step for M2-mediated viral budding. In parallel, our Raman spectroscopy revealed small but statistically significant changes in hydrocarbon chain vibrational dynamics, indicative of minor disordering in lipid chain conformation. Our findings provide useful insights into the complex interplay between transmembrane peptides and lipid bilayers, highlighting the significance of peptide-lipid interactions in modulating membrane structure, mechanics, and molecular dynamics.

Generation of biosurfactants by P. aeruginosa gi |KP163922| on waste engine oil in a free and immobilized cells system

AbstractThis study investigated biosurfactant production by the bacterial strain of P. aeruginosa gi |KP 163922| for a free and immobilized cells system using waste engine oil (WEO) as a substrate. The polyurethane foam (PUF) cubes (1 cm × 1 cm × 1 cm) were used as carriers for the immobilization. The batch experiments were performed in Erlenmeyer flasks and monitored at every 24‐h interval for both cell systems. The microbial population was counted using the plate count method, and the hydrocarbon degradation percentage was calculated to evaluate the bacterial activity. Surface tension was measured at regular intervals to ensure the presence of biosurfactants. The maximum reduction was 37 and 35 mN/m in a free and immobilized cells system. Immobilization of cells using PUF was found to be efficient in supporting bacterial growth, and after 48 h of incubation, the growth was 2.5 (±0.58) × 1011 CFU/mL. The chemical characterization using Fourier transform infrared (FTIR) spectroscopy confirmed the obtained product as rhamnolipid. Crude biosurfactant yield was found to be maximum in the case of the immobilized system, which was approximately 18 g/L. Scanning electron micrographs (SEM) of the used PUF cubes showed the strong adherence of biofilm to the cube surface and the potential of its reuse in multiple cycles. Gas chromatography–mass spectrometry (GC–MS) analysis confirms that the immobilized strain of P. aeruginosa exhibited superior biodegradation capabilities compared to free cells. Specifically, it was capable of reducing the concentration of polyaromatic hydrocarbons and converting more significant aliphatic compounds into metabolic byproducts such as alkanes, alkenes, cycloalkanes, and carbonyl groups.

Synthesis of metal-free heteroatom (N, P, O, and B) doped biochar catalysts for enhanced catalytic co-pyrolysis of walnut shells and palm oil fatty acid distillate to produce high-quality bio-oil

In the current study, sugarcane bagasse-derived biochar catalysts were synthesized by doping with metal-free heteroatoms including nitrogen, phosphorus, oxygen, and boron and their efficacy was tested for catalytic co-pyrolysis of walnut shells (WS) and palm oil fatty acid distillate (PFAD) using Py-GC/MS. The biochar catalysts’ properties and their effectiveness on co-pyrolytic bio-oil (overall product distribution, selectivity towards aliphatic and aromatic hydrocarbons, and carbon number ranges) were extensively examined. Among the various catalysts considered, boron-doped biochar (BCB) demonstrated effective performance due to an improved surface area, porosity, and acidity and resulted in a significantly increased hydrocarbon yield, particularly in the gasoline and diesel range, and preference for aromatic over aliphatic hydrocarbons. The optimum bio-oil quality was achieved at a feedstock-to-catalyst ratio of 2:1 and a pyrolysis temperature of 750 °C, with a hydrocarbon yield of 90.8 % and aromatic hydrocarbon selectivity of 63.5 %. Overall, the study underscores the role of BCB in fostering deoxygenation, decarboxylation, and aromatic selectivity via thermal and catalytic pathways, highlighting the potential of non-metallic doped biochars for bio-oil upgrading.

Characterization of Low-Molecular-Weight Dissolved Organic Matter Using Optional Dialysis and Orbitrap Mass Spectrometry.

Low-molecular-weight (LMW, <1000 Da) dissolved organic matter (DOM) plays a significant role in metal/organic pollutant complexation, as well as photochemical/microbiological processes in freshwater ecosystems. The micro size and high reactivity of LMW-DOM hinder its precise characterization. In this study, Suwannee River fulvic acid (SRFA), a commonly used reference material for aquatic DOM, was applied to examine the optical features and molecular composition of LMW-DOM by combining membrane separation, ultraviolet-visible absorption and Orbitrap mass spectrometry (MS) characterization. The 100-500 Da molecular weight cut-off (MWCO) membrane had a better performance in regard to separating the tested LMW-DOM relative to the 500-1000 Da MWCO membrane. The ultraviolet-visible absorbance decreased dramatically for the retentates, whereas it increased for the dialysates. Specifically, carbohydrates, lipids and peptides exhibited high selectivity to the 100-500 Da MWCO membrane in early dialysis. Lignins, tannins and condensed aromatic molecules displayed high permeability to the 500-1000 Da MWCO membrane in late dialysis. Overall, the retentates were dominated by aromatic rings and phenolic hydroxyls with high O/Cwa (weighted average of O/C) and low H/Cwa. Conversely, such dialysates had numerous aliphatic chains with high H/Cwa and low O/Cwa compared to SRFA. In particular, LMW-DOM below 200 Da was identified by Orbitrap MS. This work provides an operational program for identifying LMW-DOM based on the SRFA standard and MS analysis.

Preparation and Properties of Composite Double-Network Gel for Inhibiting Coal Spontaneous Combustion.

In order to improve the inhibition effect of gel on coal spontaneous combustion, a chitosan (CS)/polyacrylamide (PAM)/metal ion (Al3+) composite double-network gel was developed in this study. The optimum formula of the composite double-network gel was determined using orthogonal experimentation. The microstructure, water retention, compressibility, and anti-destruction properties of the composite double-network gel were analyzed. The inhibition effect of the composite double-network gel on coal spontaneous combustion was studied via infrared spectroscopy and a synchronous thermal analyzer from the micro and macro perspectives. The results show that the composite double-network gel has a denser interpenetrating double-network structure and a larger void ratio than the ordinary gel. The water retention rate was 55% after standing at 150 °C for 12 h. The deformation memory ratio of the composite double-network gel was 78%, which was 26.8% higher than that of the ordinary gel, and the compressive strength also increased by 59.96%. In addition, the critical temperature point and the maximum thermal weight-loss rate temperature point decreased by 7.01 °C and 39.62 °C, respectively, and the composite double-network gel effectively reduced active functional groups in the treated coal sample, such as hydroxyl and aliphatic hydrocarbons. In this study, a CS/PAM/Al3+ composite double-network gel was produced, which exhibited good gel performance and inhibition effects, with physical effects such as the covering, wetting, and cementation of coal.

Source differentiation of BTEX compounds in groundwater contaminated due to refinery activities

This study aims to identify sources of groundwater contamination in a refinery area using integrated compound-specific stable isotope analysis (CSIA), oil fingerprinting techniques, hydrogeological data, and distillation analysis. The investigations focused on determination of the origin of benzene, toluene, ethylbenzene, and xylenes (BTEX), and aliphatic hydrocarbons as well. Groundwater and floating oil samples were collected from extraction wells for analysis. Results indicate presence of active leaks in both the northern and southern zones. In the northern zone, toluene was found to primarily originate from oil products like aviation turbine kerosene (ATK or aviation fuel), kerosene, regular gasoline, and diesel fuel. Additionally, stable isotope ratios of carbon and hydrogen for ethylbenzene, o-xylene (ortho xylene) and p-xylene (para xylene) in zone A suggested the pollution originated from gasoline within the northern zone. The origin of super gasoline (with higher octane) identified in southern zone using δ13C and δ2H values of toluene in the floating oil and groundwater samples. Further, biodegradation of toluene likely occurred in southern zone according to δ13C and δ2H. The findings underscore the critical importance of integrating CSIA and fingerprinting techniques to effectively address the challenges of source identification and relying solely on each method independently is insufficient. Accordingly, comparing the GC-MS results of floating oil samples with ATK and jet fuel (JP4) standards can be effectively utilized for source differentiation. However, this method showed no practical application to distinguish different types of diesel or gasoline. The accuracy and reliability of source identification of BTEX compounds may significantly improve when hydrogeological data incorporates with stable isotopes analysis. Additionally, the results of this study will elevate the procedures for fuel-related contaminants source identification of the polluted groundwater that is crucial to develop effective remediation strategies.

Plasmid DNA Complexes in Powder Form Studied by Spectroscopic and Diffraction Methods.

Currently, new functional materials are being created with a strong emphasis on their ecological aspect. Materials and devices based on DNA biopolymers, being environmentally friendly, are therefore very interesting from the point of view of applications. In this paper, we present the results of research on complexes in the powder form based on plasmid DNA (pDNA) and three surfactants with aliphatic chains containing 16 carbon atoms (cetyltrimethylammonium chloride, benzyldimethylhexadecylammonium chloride and hexadecylpyridinium chloride). The X-ray diffraction results indicate a local hexagonal packing of DNA helices in plasmid DNA complexes, resembling the packing for corresponding complexes based on linear DNA. Based on the Fourier-transform infrared spectroscopy results, the DNA conformation in all three complexes was determined as predominantly of A-type. The two relaxation processes revealed by dielectric spectroscopy for all the studied complexes are connected with two different contributions to total conductivity (crystallite part and grain boundaries). The crystallite part (grain interior) was interpreted as an oscillation of the polar surfactant head groups and is dependent on the conformation of the surfactant chain. The influence of the DNA type on the properties of the complexes is discussed, taking into account our previous results for complexes based on linear DNA. We showed that the type of DNA has an impact on the properties of the complexes, which has not been demonstrated so far. It was also found that the layer of pDNA-surfactant complexes can be used as a layer with variable specific electric conductivity by selecting the frequency, which is interesting from an application point of view.

Synergistic Interaction during Copyrolysis of Soybean Straw and Tire Waste: Improving Emissions and Product Quality.

This study explores copyrolysis of soybean straw (SS) with hydrogen-rich tire waste (TW) to enhance pyrolytic product quality and reduce pollutant emissions. Addition of TW increased SS biomass conversion from 67.19 to 72.46% and decreased coke/residue formation from 32.81 to 27.54%. The activation energy dropped to 121.84 kJ/mol from 160.73 kJ/mol (as calculated by the Kissinger-Akahira-Sunose method) and 122.78 kJ/mol from 159.76 kJ/mol (as calculated by the Ozawa-Flynn-Wall method). Thermogravimetric analysis coupled with Fourier-transform infrared spectroscopy (TG-FTIR) showed lowered CO2, NO2, and SO2 emissions (5.58, 5.72, 3.38) compared to conventional SS pyrolysis (18.38, 11.55, 12.37). Yields of value-added chemicals (phenols, olefins, aromatics) increased (32.38, 22.17, 30.18%) versus conventional SS pyrolysis (23.56, 13.78, 20.36%). Pyrolysis gas chromatography-mass spectrometry (Py/GC-MS) analysis reveals that the addition of TW leads to a decrease in the production of oxygenates and polycyclic aromatic hydrocarbons, reducing their yields to 8.96 and 7.67%, respectively, down from 19.37 and 14.37%. Simultaneously, it enhances the yields of olefins, aromatics, phenols, and aliphatic hydrocarbons to 23.38, 26.78, 26.17, and 25.78%, respectively, compared to 15.37%, 15.29, 18.36, and 17.25%, respectively, in the absence of TW. In summary, copyrolysis of TW with SS improves product quality and reduces pollutant emissions, marking a significant research contribution.

Green Synthesis of Silver Nanoparticles With Cyclosorus dentatus and Nephrolepis biserrata and Their Antioxidant, Anti‐Inflammatory Studies

ABSTRACTThis study examined the synthesis of silver nanoparticles (SNPs) with aqueous extracts of Cyclosorus dentatus and Nephrolepis biserrata fronds and the evaluation of their biological activities. Mixing of AgNO3 solution and the aqueous extracts resulted in color change, indicating the formation of SNPs. UV‐Vis spectroscopy analysis gave a surface plasmon resonance (SPR) peak at approximately 420 nm, confirming the presence of the synthesized SNPs. Infrared analysis showed C‐O, N‐O, and C‐C vibrations or stretching and aliphatic vibrations of hydrocarbon chains of the synthesized SNPs. x‐Ray diffraction (XRD) analysis indicated the SNPs were face‐centered, cubic, and crystalline in nature, with crystallite sizes. The scanning electron microscopy (SEM) shows the aggregation of the spherical shape nanoparticles. The SNPs significantly reduced phosphomolybdenum and captured H2O2 with respective IC50 values of 61.55 and 29.03 µg/mL for C. dentatus SNP (SNP‐Cd), and 92.61 and 9.07 µg/mL for N. biserrata SNP (SNP‐Nb), respectively. In terms of albumin‐denaturing activity, the SNPs gave an IC50 value of 21.20 µg/mL for SNP‐Cd and 7.18 µg/mL for SNP‐Nb. Thus, this work confirmed that SNP‐Cd and SNP‐Nb are potential therapeutic agents for treating oxidative stress, inflammatory problems, and related diseases.

Experimental Correlation between Apparent pKa and Gelation Propensity in Amphiphilic Hydrogelators Derived from l-Dopa.

We report the gelation propensity of three gelators derived from l-dihydroxyphenylalanine (l-Dopa), where the amino group is derivatized with three different fatty acids (lauric acid, palmitic acid, and azelaic acid). The long aliphatic side chains should introduce additional van der Waals interactions among the molecules, contributing to the self-assembly process. The hydrogels have been prepared with the pH change method, and both the hydrogels and the corresponding aerogels have been analyzed using several techniques. In any case, Lau-Dopa provides stronger hydrogels compared with the other gelators. This property may be ascribed to its tendency to efficiently form supramolecular β-sheet structures, as outlined by the ECD, IR, and SEM analyses. Moreover, the preliminary measurement of the apparent pKa displays for Lau-Dopa two plateaux, as previously observed for, one at about pH 12 and a second one at pH 7.5. Thus, its pKa results in two apparent pKa shifts of ∼8.5 and ∼4 pH units above the theoretical pKa, as a consequence of a multistep self-assembly pathway that correlates, in the final β-sheet-based hydrogel, with a high degree of order and stability.

Structure characteristics and combustion kinetics of the co-pyrolytic char of rice straw and coal gangue

Co-combustion is a technology that enables the simultaneous and efficient utilization of biomass and coal gangue (CG). Nevertheless, the factors that affect the combustibility of co-pyrolytic char, which represents the rate-determining step of the entire co-combustion process, remain unclear. This study investigates the impact of the physicochemical properties of co-pyrolytic char, including pore structure, carbon structure, and alkali metals, on the combustion characteristics. The TGA analysis indicates that the ignition and burnout temperatures of the co-pyrolytic char increase as the CG mixing ratio increases, resulting in a prolonged combustion. This is due to the fact that the carbon structure of the co-pyrolytic char becomes increasingly aromatic, accompanied by a reduction in aliphatic hydrocarbons and oxygen-containing groups as the CG mixing ratio increases. Furthermore, the high ash content of the CG is another significant factor contributing to the observed reduction in combustibility. The reaction between mullite, quartz in CG, and alkali metals in biomass results in the formation of aluminosilicate, which reduces the catalytic ability of alkali metals. Furthermore, the char combustion kinetics are analyzed by the KAS method, and the results indicate that the introduction of CG increases the activation energy of the entire char combustion process. The activation energy of the 80RS20CG is within the range of 102.22–164.99 kJ/mol, while the RS char is within the range of 89.87–144.67 kJ/mol.

Catabolic gene indices of hydrocarbon diminution in Ultisol treated with cropped Bacillus altitudinis-amendments

This study evaluated catabolic gene expression as an index of hydrocarbon breakdown in ultisol treated with Bacillus altitudinis-Cropped Biofertilizers derived from Biosolid and Brewer Spent Grain (BSG) using phenotypic and molecular methods. We observed significant reductions in Total Petroleum Hydrocarbons (TPH) concentrations with both amendments, albeit the biosolid based amendment was markedly more effective. Concurrently, there was a substantial increase in hydrocarbon-degrading bacteria. Notably, the bulk of Operational Taxonomic Units (OTUs) in biosolid (95.77 %) and BSG (93.00 %) amended Ultisol were Proteobacteria, Acidobacteria, Actinobacteria, and Planctomycetes, which are key players in hydrocarbon bioremediation. We observed the presence of eleven hydrocarbon-degrading genes through M5nr analysis. These genes encompass essential catalysts for aliphatic hydrocarbon degradation and hydrocarbon desulfurization. Notably, these enzymes/genes include Bacterial Flavin-bound Monooxygenase (AlmA), Alkane Monooxygenase (AlkM), Alpha Ketoglutarate Dependent Dioxygenase (alkB), Propane Monooxygenase (PrM), Cytochrome P450 (cP450), Methane Monooxygenase/Ammonia Monooxygenase (MMO/AMO) subunits A, B, and C, Alkane Sulfonate Monooxygenase (ssuD), Alkane Sulfonates Transport System Permease Protein (ssuC), Dibenzothiophene Monooxygenase (dszC), Dibenzothiophene-Sulfone Monooxygenase (dszA), and Dibenzothiophene-5,5-Dioxide Monooxygenase (dszB). These genes play pivotal roles in the degradation of aliphatic hydrocarbons and hydrocarbon desulfurization. Interestingly, unique gene expression patterns were observed for each amendment, with Actinomycetales and Bulkhoderiales orders expressing the majority of identified genes. These findings have revealed the amendment-specific microbial and genetic alterations and, the diversity and potential of the annotated genes induced by the Bacillus altitudinis-Cropped Biofertilizers (biosolid and BSG amendments) for effective remediation of hydrocarbon-contaminated soils.

Spectro-photometry of Phobos simulants: I. Detectability of hydrated minerals and organic bands

Previous Mars Reconnaissance Orbiter and Mars Express observations of Phobos and Deimos, the moons of Mars, have improved our understanding of these small bodies. However, their formation and composition remain poorly constrained. Physical and spectral properties suggest that Phobos may be a weakly thermal-altered captured asteroid but the dynamical properties of the martian system suggest a formation by giant collision similar to the Earth moon. In 2027, the JAXA’s MMX mission aims to address these outstanding questions.We undertook measurements with a new simulant called OPPS (Observatory of Paris Phobos Simulant) which closely matches Phobos reflectance spectra from the visible to the mid-infrared wavelength range. The simulant was synthesized using a mixture of olivine, saponite, anthracite, and coal.Since observation geometry strongly influences the photometry and spectra of the light reflected from planetary surfaces, we evaluated the parameters obtained by modeling the phase curves – obtained through laboratory measurements – of two different Phobos simulants (UTPS-TB and OPPS) using Hapke IMSA model. Our results show that the photometric properties of Phobos simulants are not fully consistent with those of carbonaceous chondrites and martian meteorites. We also investigated the detection of volatiles/organic compounds and hydrated minerals, as the presence of such components is expected on Phobos in the hypothesis of a captured primitive asteroid. To investigate their detectability, we examined the variability of the 3.28μm and 3.42μm absorption bands related to aliphatic/aromatic carbon (as a proxy of organic material), as well as the 2.7μm O–H feature in a Phobos laboratory spectroscopic simulant. The results indicate that a significant amount of organic compounds is required for the detection of C–H bands at 3.4μm. The bands at 3.28 and 3.42μm are faint (less than 2%) when ∼3 wt% of organic compounds are present in the simulant and are likely undetectable by the MIRS spectrometer onboard the MMX mission. When the concentration of aliphatic and aromatic compounds is increased to 6 wt%, a positive detection starts to become more plausible using remote sensing infrared spectroscopy. In contrast, the 2.7μm absorption band, due to hydrated minerals, is much deeper and easier to detect than C–H organic features at the same concentration levels. The feature is still clearly detectable even when the simulant contains only 3 vol.% of phyllosilicates, corresponding to 0.7 wt% OH groups.Posing limits on detectability of some possible key components of Phobos surface will be pivotal to prepare and interpret future observations of the MIRS spectrometer as well as TENGOO and OROCHI cameras onboard MMX mission.

Pyrolysis-catalysis of waste tire to enhance the aromatics selectivity via metal-modified ZSM-5 catalysts

Excessive untreated waste tires (WT) have posed threats to the environment and human health. Pyrolysis-catalysis, as a promising treatment technology, could convert WT into high-valued products such as pyrolysis oil. Moreover, BTX compounds (Benzene, toluene, and xylene) were important raw materials in the chemical industry. In order to sharply increase the BTX selectivity in the pyrolytic oil, transition metals (Ni and Fe) were impregnated on the ZSM-5 catalyst. Furthermore, this paper also explored the effect of catalysis modes, catalysts-to-feedstock mass ratios, and catalysis temperatures on the distribution of the aromatics in the WT pyrolysis-catalysis oil. The results suggested that the optimal operating parameters for BTX compound production with a selectivity of 39.87% were in-situ mode, catalysis temperature=600 °C, and catalyst-to-feedstock mass ratio=1:1 by applying Ni/ZSM-5. According to the GC-MS identification results, it proposed that the Diels-Alder reaction of isoprene and cracking and recombination of limonene in the aliphatic hydrocarbon pool were the main paths to generate the aromatics, while the addition of ethylene radicals in the monocyclic aromatic hydrocarbon (MAH) and polycyclic aromatic hydrocarbon (PAH) pools was dominant in the growth of the aromatics. The study provided a viable approach for upgrading WT to produce high-value aromatic products.