Search Results (90)

The continued acidification of red soil reduces phosphorus availability and microbial activity, which restricts corn growth. Phosphorus tailings, a waste product from phosphate mining, can neutralize soil acidity and supply controlled-release phosphorus, but their effects on the red soil-corn system remain unclear. A field experiment in Qujing, Yunnan (2023–2024), tested four treatments: CK (standard fertilization), T1 (CK plus phosphorus tailings), T2 (80% of standard fertilizer plus phosphorus tailings), and T3 (80% of standard fertilizer plus phosphorus tailings and organic fertilizer, both applied at 6.0 t·ha⁻¹). Using high-throughput sequencing, redundancy analysis (RDA), and structural equation modeling (SEM), the study evaluated impacts on soil properties, microbial communities, and corn yield and quality. Results showed: (1) Phosphorus tailings reduced soil acidification; T3 raised soil pH in the top 0–10 cm by 0.54–0.9 units compared to CK and increased total, available, and soluble phosphorus in the 0–20 cm layer to 952.82, 28.46, and 2.04 mg/kg, respectively. (2) T3 exhibited the highest microbial diversity (Chao1 and Shannon indices increased by 177.57% and 37.80% versus CK) and a more complex bacterial co-occurrence network (114 edges versus 107 in CK), indicating enhanced breakdown of aromatic compounds. (3) Corn yield under T3 improved by 13.72% over CK, with increases in hundred-grain weight (+6.02%), protein content (+18.04%), and crude fiber (+9.00%). (4) Effective nitrogen, ammonium nitrogen, available phosphorus, and soil conductivity were key factors affecting gcd/phoD phosphorus-reducing bacteria. (5) Phosphorus tailings indirectly increased yield by modifying soil properties and pH, both positively linked to yield, while gcd-carrying bacteria had a modest positive influence. In summary, combining phosphorus tailings with a 20% reduction in chemical fertilizer reduces fertilizer use, recycles mining waste, and boosts corn production in acidic red soil, though further studies are needed to evaluate long-term environmental effects. Full article

Three-dimensional/two-dimensional bilayered perovskite solar cells have recently become popular for ensuring high efficiency and promising long-term stability. The 3D/2D bilayered perovskite thin film is mainly used in regular (n-i-p)-type perovskite solar cells. In this review, our discussion also focuses on the regular kind of perovskite solar cells. In a 3D/2D bilayered perovskite thin film, the 2D perovskite layer works as a capping layer on top of the 3D perovskite thin film. The 2D capping layer heals the surface and bulk defects of the 3D perovskite thin film. The 2D layer interfaces between the 3D perovskite and hole transport layers. The 2D layer also acts as a shield against moisture and heat. This layer also inhibits ion migration between layers (3D perovskite and back contact). This review lists and investigates different organic precursors deposited as a 2D capping layer on top of the 3D perovskite thin film to explore their impact on the solar cell’s efficiency and stability. The possible challenges and remedies in growing a 2D capping layer on top of the 3D perovskite thin film are also discussed. Full article

Petroleum hydrocarbon contamination has emerged as a significant global environmental issue, severely impacting soil microbial communities and their functions. This study employed high-throughput sequencing to systematically analyze the bacterial community structure and functional genes in soils with varying levels of petroleum hydrocarbon contamination. The results demonstrated that petroleum contamination led to a significant decline in microbial diversity, while enhancing the abundance of specific functional genes, such as those involved in polycyclic aromatic hydrocarbon (PAH) degradation, methane production, and denitrification. Phylogenetic analysis further revealed that microbial communities in highly contaminated soils tended to form highly clustered and specialized groups, while simultaneously promoting the coexistence of phylogenetically distant microorganisms. The Mantel test identified significant correlations between ammonium ion concentration, soil moisture content, and microbial metabolic pathways, particularly those related to petroleum hydrocarbon degradation and denitrification. These findings suggest that petroleum contamination not only disrupts the carbon and nitrogen metabolism balance but also has profound implications for greenhouse gas emissions and nitrogen cycling, potentially destabilizing the ecosystem. This study provides novel insights into the ecological functions of microbial communities in petroleum-contaminated soils and highlights potential key factors for pollution management and ecological restoration. Full article

Thiophenol (synonyms: phenyl mercaptan, benzenethiol) may appear in the aquatic environment as a result of human activity. It is used as a raw material in organic synthesis in various industries for the production of dyes, pesticides, pharmaceuticals and polymers, such as polyphenylene sulfide (PPS). It may also enter water through contamination with petroleum substances (thiophenol may be present in crude oil). Due to the fact that thiophenol is toxic to living organisms, its removal from water can be a very important task. For the first time, this paper presents experimental studies of the sorption and desorption process of thiophenol on an ion exchange resin. Thiophenol sorption experiments on AmbeLite^®IRA402 (Cl form) were tested at different pH levels (4, 7, and 9) and different ionic strengths of the aqueous solution. Its detection in water was carried out using UV spectroscopy. At pH 4, the thiophenol sorption process is basically independent of the ionic strength of the solution, but also the least effective. The sorption capacity of a thiophenol solution in distilled water is about 0.37–0.46 mg/g, for a solution with an ionic strength of 0.1 M 0.42 mg/g. At pH 7 and 9, the sorption of thiophenol from an aqueous solution is similar and definitely more effective. The sorption capacity of the thiophenol solution in distilled water is about 13.83–14.67 mg/g, and for a solution with an ionic strength of 0.1 M, it is 2.83–2.10 mg/g. The desorption efficiency of thiophenol from AmbeLite^®IRA402 resin (washing with 4% HCl) at pH 7 is 90%, which is promising for the resin reuse process. Kinetic studies were performed and a pseudo-first-order and second-order kinetic model was fitted to the obtained experimental sorption data. In most cases, the simulation showed that the pseudo-second-order model gives a better fit, especially for the sorption of thiophenol from the solution with an ionic strength of 0.1 M. The fit of the Freundlich and Langmuir isotherm models to the experimental results indicates that the latter model provides better agreement. Analysis of the infrared spectra supported by quantum chemical calculations (DFT/PCM/B3LYP/6-31g**) confirms the experimental results observed during the sorption process. At pH 7 and 9, the thiophenol is sorbed in anionic form and—together with the ion exchange processes that occur between the dissociated thiol group and the quaternary ammonium group—an interaction between the aromatic structures of thiophenolate anions and IRA402 also takes place. Full article

The interaction of sodium phytate hydrate C₆H₁₈O₂₄P₆·xNa·yH₂O (phytNa) with Cu(OAc)₂·H₂O and 1,10-phenanthroline (phen) led to the anionic tetranuclear complex [Cu₄(H₂O)₄(phen)₄(phyt)]·2Na⁺·2NH₄⁺·32H₂O (1), the structure of the latter was determined by X-ray diffraction analysis. The phytate 1 is completely deprotonated; six phosphate⁻ fragments (with atoms P1–P6) are characterized by different spatial arrangements relative to the cyclohexane ring (1a5e conformation), which determines two different types of coordination to the complexing agents—P1 and P3, P4, and P6 have monodentate, while P2 and P5 are bidentately bound to Cu²⁺ cations. The molecular structure of the anion complex is stabilized by a set of strong intramolecular hydrogen bonds involving coordinated water molecules. Aromatic systems of phen ligands chelating copper ions participate in strong intramolecular and intermolecular π-π interactions, further contributing to their association. At the supramolecular level, endless stacks are formed, in the voids of which sodium and ammonium cations and water molecules are present. The stability of 1 in the presence of human serum albumin (HSA) was investigated using Electron Paramagnetic Resonance (EPR) spectroscopy. Continuous wave (CW) EPR spectra in water/glycerol frozen solution clearly indicate a presence of an exchange-coupled Cu(II)-Cu(II) dimeric unit, as well as a Cu(II) monomer-like signal arising from spins sufficiently distant from each other, with comparable contributions of two types of signals. In the presence of albumin at a 1:1 ratio (1 to albumin), the EPR spectrum changes significantly, primarily due to the reduced contribution of the S = 1 fraction showing dipole–dipole splitting. The biological activity of 1 in vitro against the non-pathogenic (model for Mycobacterium tuberculosis) strain of Mycolicibacterium smegmatis is comparable to the first-line drug for tuberculosis treatment, rifampicin. Full article

In this work, we present new methods of synthesis of different molecules including a 2-pyridone nucleus. First, we prepared a series of 1H-free 2-pyridones and N-alkyl 2-pyridones from ethyl cyanoacetate, aromatic aldehydes, various acetophenone derivatives and ammonium acetate or diamino-alkane. These molecules have served as building blocks that, in conjunction with acyl chloride derivatives, glycoside derivatives, etc. have resulted in various heterocyclic hybrid structures carrying a 2-pyridone ring. Moreover, based on the cyano group reactivity of the 2-pyridone ring, we synthesized 5-pyridone 1H-tetrazole in a single step by a cycloaddition reaction [3 + 2] between 3-cyano-2-pyridone nitriles and sodium azide in the presence of metal-free L-proline. Full article

Tryptophan is an essential aromatic amino acid widely used in the pharmaceutical, agricultural, and feed industries. Microbial fermentation, mainly using Escherichia coli, has become the preferred method for its production due to sustainability and lower costs. Optimizing tryptophan production requires careful control of various fermentation parameters, including nutrients, pH, temperature, and dissolved oxygen (DO) levels. Glucose, as the primary carbon source, must be fed at controlled rates to avoid metabolic overflow, which leads to by-product accumulation and reduced production efficiency. Nitrogen sources, both organic (such as yeast extract) and inorganic (like ammonium), influence biomass growth and tryptophan yield, with ammonium levels requiring careful regulation to avoid toxic accumulation. Phosphate enhances growth but can lead to by-product formation if used excessively. pH is another critical factor, with an optimal range between 6.5 and 7.2, where enzyme activity is maximized. Temperature control promotes growth and production, particularly between 30 °C and 37 °C. High DO levels increase tryptophan titers by boosting the pentose phosphate pathway and reducing by-products like acetate. Furthermore, surfactants and supplements such as betaine monohydrate and citrate help alleviate osmotic stress and enhance precursor availability, improving production efficiency. Careful manipulation of these parameters allows for high-density cell cultures and significant tryptophan accumulation, making microbial fermentation competitive for large-scale production. Full article

Rhizosphere microorganisms play a pivotal role in biogeochemical cycles, particularly in relation to carbon (C) and nitrogen (N) cycles. However, the impact of stand age on the composition of rhizosphere microbial communities and the abundance involved in C and N cycling remains largely unexplored in restoration ecosystems dominated by shrubs of temperate deserts. This study focuses on revealing changes in microbial composition and functional genes in the rhizosphere soil of Caragana korshinskii after revegetation, as well as their response mechanisms to changes in environmental factors. The alpha diversity of bacteria tended to increase with stand age, whereas that of fungi decreased. The abundance of denitrification; dissimilatory nitrate reduction to ammonium, nitrification, and ammonium assimilation; and C fixation-related gene levels increased with stand age, whereas those related to the degradation of starch, pectin, hemicellulose, cellulose, and aromatics decreased. The parameters MBC, MBN, and TC were the key factors affecting the bacterial community, whereas the fungal community was regulated by TN, EC, pH, and MBC. Stand age indirectly regulated C and N cycling functions of genes through altered soil properties and microbial community structures. This study presents a novel approach to accurately evaluate the C and N cycling dynamics within ecosystems at various stages of restoration. Full article

Catalytic biomass pyrolysis is one of the most promising routes for obtaining bio-sustainable products that replace petroleum derivatives. This study evaluates the production of aromatic compounds (benzene, toluene, and xylene (BTX)) from the catalytic pyrolysis of lignocellulosic biomass (Pinus radiata (PR) and Eucalyptus globulus (EG)). Chilean natural zeolite (NZ) was used as a catalyst for pyrolysis reactions, which was modified by double ion exchange (H2NZ) and transition metals impregnation (Cu5H2NZ and Ni5H2NZ). The catalysts were characterized by nitrogen adsorption, X-ray diffraction (XRD), ammonium programmed desorption (TPD-NH₃), and scanning electron microscopy with energy dispersive X-ray spectroscopy (SEM-EDS). Analytical pyrolysis coupled with gas chromatography/mass spectrometry (Py-GC/MS) allowed us to study the influence of natural and modified zeolite catalysts on BTX production. XRD analysis confirmed the presence of metal oxides (CuO and NiO) in the zeolite framework, and SEM-EDS confirmed successful metal impregnation (6.20% for Cu5H2NZ and 6.97% for Ni5H2NZ). Py-GC/MS revealed a reduction in oxygenated compounds such as esters, ketones, and phenols, along with an increase in aromatic compounds in PR from 2.92% w/w (without catalyst) to 20.89% w/w with Ni5H2NZ at a biomass/catalyst ratio of 1/5, and in EG from 2.69% w/w (without catalyst) to 30.53% w/w with Ni5H2NZ at a biomass/catalyst ratio of 1/2.5. These increases can be attributed to acidic sites within the catalyst pores or on their surface, facilitating deoxygenation reactions such as dehydration, decarboxylation, decarbonylation, aldol condensation, and aromatization. Overall, this study demonstrated that the catalytic biomass pyrolysis process using Chilean natural zeolite modified with double ion exchange and impregnated with transition metals (Cu and Ni) could be highly advantageous for achieving significant conversion of oxygenated compounds into hydrocarbons and, consequently, improving the quality of the condensed pyrolysis vapors. Full article

Lignocellulosic materials, made up of cellulose, hemicellulose, and lignin, constitute some of the most prevalent types of biopolymers in marine ecosystems. The degree to which marine microorganisms participate in the breakdown of lignin and their impact on the cycling of carbon in the oceans is not well understood. Strain LCG002, a novel Marivivens species isolated from Lu Chao Harbor’s intertidal seawater, is distinguished by its ability to metabolize lignin and various aromatic compounds, including benzoate, 3-hydroxybenzoate, 4-hydroxybenzoate and phenylacetate. It also demonstrates a broad range of carbon source utilization, including carbohydrates, amino acids and carboxylates. Furthermore, it can oxidize inorganic gases, such as hydrogen and carbon monoxide, providing alternative energy sources in diverse marine environments. Its diversity of nitrogen metabolism is supported by nitrate/nitrite, urea, ammonium, putrescine transporters, as well as assimilatory nitrate reductase. For sulfur assimilation, it employs various pathways to utilize organic and inorganic substrates, including the SOX system and DSMP utilization. Overall, LCG002’s metabolic versatility and genetic profile contribute to its ecological significance in marine environments, particularly in the degradation of lignocellulosic material and aromatic monomers. Full article

This study demonstrates the synthesis of five novel quaternary ammonium aldimines through a two-step synthetic route involving a condensation reaction between 4-pyridincarboxyaldehyde and 3,4,5-trimethoxyaniline, followed by the quaternization of the pyridine N-atom with various aromatic α-bromo ketones. The newly obtained compounds underwent characterization for both purity and molecular structure, utilizing HR-MS, 1D, and 2D NMR spectroscopy in solution, as well as a comparison between single-crystal and powder X-ray analyses in a solid state. The thermal behavior of the studied compounds was evaluated using differential scanning calorimetry (DSC). The antioxidant properties of the compounds were assessed through DPPH (2,2-diphenyl-1-picrylhydrazyl) radical scavenging and ferric-reducing antioxidant power (FRAP) assays, employing Trolox as a standard. The performed in vitro antibacterial screening indicates a selective antibacterial activity against Gram-negative K. pneumoniae and P. aeruginosa, while no such activity is detected for Gram-negative E. coli and Gram-positive S. aureus. Full article

A series of quaternary ammonium or phosphonium salts were applied as zeolite growth modifiers in the synthesis of hierarchical ZSM-5 zeolite. The results showed that the use of methyltriphenylphosphonium bromide (MTBBP) could yield nano-sized hierarchical ZSM-5 zeolite with a “rice crust” morphology feature, which demonstrates a better catalytic performance than other disinfect candidates. It was confirmed that the addition of MTBBP did not cause discernable adverse effects on the microstructures or acidities of ZSM-5, but it led to the creation of abundant meso- to marco- pores as a result of aligned tiny particle aggregations. Moreover, the generation of the special morphology was believed to be a result of the coordination and competition between MTBBP and Na⁺ cations. The as-synthesized hierarchical zeolite was loaded with Zn and utilized in the propane aromatization reaction, which displayed a prolonged lifetime (1430 min vs. 290 min compared with conventional ZSM-5) and an enhanced total turnover number that is four folds of the traditional one, owing to the attenuated hydride transfer reaction and slow coking rate. This work provides a new method to alter the morphological properties of zeolites with low-cost disinfectants, which is of great potential for industrial applications. Full article

During adaptation to waters that are rich in xenobiotics, biological systems pass through multiple stages. The first one is related to the restructuring of communities, pronounced destruction of the structure, and multiplication of active biodegradants. The purpose of the present research was to describe the microbiome restructuring that occurs during the adaptation stage in landfill leachate treatment. In a model SBR (sequencing batch reactor), a 21-day purification process of landfill leachate was simulated. Wastewater was fed in increasing concentrations. When undiluted leachate entered, the activated sludge structure disintegrated (Sludge Volume Index—4.6 mL/g). The Chemical Oxygen Demand and ammonium nitrogen concentration remained at high values in the influent (2321.11 mgO₂/L and 573.20 mg/L, respectively). A significant amount of free-swimming cells was found, and the number of aerobic heterotrophs and bacteria of the genera Pseudomonas and Acinetobacter increased by up to 125 times. The Azoarcus-Thauera cluster (27%) and Pseudomonas spp. (16%) were registered as the main bacterial groups in the activated sludge. In the changed structure of the microbial community, Gammaproteobacteria, family Rhizobiaceae, class Saccharimonadia were predominantly represented. Among the suspended bacteria, Microbactericeae and Burkholderiaceae, which are known for their ability to degrade xenobiotics, were present in larger quantities. The enzymological analysis demonstrated that the ortho-pathway of cleavage of aromatic structures was active in the community. The described changes in the leachate-purifying microbial community appear to be destructive at the technological level. At the microbiological level, however, trends of initial adaptation were clearly outlined, which, if continued, could provide a highly efficient biodegradation community. Full article

Polycyclic aromatic hydrocarbons (PAHs) and polychlorinated biphenyls (PCBs) are recognized as carcinogens and mutagenic food contaminants that threaten public health. As for food safety aspects, control of these contaminants in processed and fatty food is necessary. In this study, eleven factors were screened by the Plackett–Burman design, and four variables were chosen to optimize with the central composite design (CCD) for the improvement of extraction and cleanup procedures of these food contaminants. The optimized variables include 5 g of sample, 2 mL mixture of 2/2/1 ethyl acetate/acetone/isooctane, 1.6 g of ammonium formate, 0.9 g of sodium chloride, and 0.25 g of sorbent Z-Sep+. A 5 min cleanup vortex time with the spike calibration curve strategy, analyzed by gas chromatography–mass spectrometry (GC-MS), led to the validated limits of quantification (LOQs) for 16 PAHs and 36 PCBs of 0.5–2 and 0.5–1 ng/g, respectively, and recoveries of 72–120%, with an average relative standard deviation (%RSD) of 17, for PAHs, and 80–120%, with an %RSD of 3, for PCBs. The method introduces excellent accuracy, precision, and efficiency, and minimizes matrix effects, and ensures a control procedure, adopted with international standards, for food authorities to determine the contaminants of interest in processed meat, and consequently, prevent food-borne disease to improve public health indices. Full article

Deep eutectic solvents (DESs) with a hydrophobic aromatic ring structure offer a promising pretreatment method for the selective delignification of lignocellulosic biomass, thereby enhancing enzymatic hydrolysis. Further investigation is needed to determine whether the increased presence of aromatic rings in hydrogen bond receptors leads to a more pronounced enhancement of lignin removal. In this study, six DES systems were prepared using lactic acid (LA)/acetic acid (AA)/levulinic acid (LEA) as hydrogen bond donors (HBD), along with two independent hydrogen bond acceptors (HBA) (benzyl triethyl ammonium chloride (TEBAC)/benzyl triphenyl phosphonium chloride (BPP)) to evaluate their ability to break down sugarcane bagasse (SCB). The pretreatment of the SCB (raw material) was carried out with the above DESs at 120 °C for 90 min with a solid–liquid ratio of 1:15. The results indicated that an increase in the number of aromatic rings may result in steric hindrance during DES pretreatment, potentially diminishing the efficacy of delignification. Notably, the use of the TEBAC:LA-based DES under mild operating conditions proved highly efficient in lignin removal, achieving 85.33 ± 0.52% for lignin removal and 98.67 ± 2.84% for cellulose recovery, respectively. The maximum digestibilities of glucan (56.85 ± 0.73%) and xylan (66.41 ± 3.06%) were attained after TEBAC:LA pretreatment. Furthermore, the maximum ethanol concentration and productivity attained from TEBAC:LA-based DES-pretreated SCB were 24.50 g/L and 0.68 g/(L·h), respectively. Finally, the comprehensive structural analyses of SCB, employing X-rays, FT-IR, and SEM techniques, provided valuable insights into the deconstruction process facilitated by different combinations of HBDs and HBAs within the DES pretreatment. Full article