Search Results (783)

Hydrocolloids are essential additives in the food industry, serving as thickening or gelling agents due to their high-water absorption capacity and viscosity even at low concentrations. This study investigates hydrocolloids extracted from Dioscorea rotundata and evaluates the effects of solubilization conditions—acidic, neutral, and alkaline—on their physicochemical, technological, rheological, and pasting properties. The hydrocolloids present extraction yields of carbohydrates similar to those of commercial ones (higher than 80%), with the presence of carboxyl groups. The retention of water and oil was greater than 100% and 2% of the solubility. All samples present a non-Newtonian flow behavior type of shear thinning adjusted to the Cross model (R² > 0.90). The viscoelastic properties denote an elastic behavior ($G\prime$ > $G″$). Hydrocolloids began to gelatinize at the same temperature (70 °C); the viscosity of the samples increased rapidly. D. rotundata is a source of hydrocolloids for use in the food industry as a thickener or additive. Full article

The aim of this work is to present a technologically feasible method for processing biomass into synthesis gas or hydrogen-rich gas. Three types of biomass with different lignin contents were pyrolyzed in a pyrolysis unit under well-defined conditions (ambient pressure, heating rate of 10 K min⁻¹, end temperature of 500 °C, operating particle size, variable catalyst mass) in the presence of a ruthenium catalyst (Ru/Al₂O₃, powder), and the effect of catalyst amount on the yield and gas composition was observed. Feedstock mass was always 50 g, and catalyst mass was 2.5, 5, and 10 g (mixing ratios 0.05, 0.1, and 0.2, resp.). During pyrolysis, the raw gas and vapors was passed through the catalyst bed and converted to the resulting gas and bio-oil. The gas obtained was cleaned by sequestration with CO₂ using commercial active carbon to obtain syngas with different H₂/CO ratios or hydrogen-rich gas. It was found that, depending on the catalyst amount, slow pyrolysis catalyzed by ruthenium yielded syngas with a H₂/CO ratio of approximately 0.5–5, which is further usable. The by-products obtained (bio-oil and biochar) are also described. Bio-oils from all three biomass types contained mainly carboxylic acids (33–46 wt.%) and phenols (18–33 wt.%), hydroquinone (up to 5 wt.%), and a high amount of stearate (up to 26 wt.%). All of these compounds have high utility value. The resulting biochar can probably be applied, after activation using CO₂, as a sorbent. In conclusion, under energy-efficient conditions (end temperature max. 500 °C), Ru/Al₂O₃-catalyzed pyrolysis of biomass provides syngas or hydrogen-rich gas and usable by-products. It should be emphasized that the maximum theoretical H₂ production from biomass is 60–70 g H₂/kg biomass. This limit value could negatively affect the technological development of the process. Full article

HPAM-Cr³⁺ (partially hydrolyzed polyacrylamide-chromium ion) gels are widely used in enhancing oil recovery (EOR) due to their advantages of low cost, controllability, and high strength. The propagation distance of gels within the reservoir significantly negatively impacts their gelation performance. However, the extent of this influence remains unclear, hindering precise optimization for field applications. This study first established a gelation performance characterization method based on visual inspection, rheological parameters, and long-term stability, accurately classifying gels into five types: stable strong gel (SSG), stable weak gel (SWG), colloidal dispersion gel (CDG), unstable gel (USG), and over-crosslinked gel (OCG). Subsequently, cross-experiments were conducted using varying concentrations of HPAM and Cr³⁺. Based on the contour map of visual appearance, storage modulus (G′), and water loss rate (R_w) of the gels, distribution maps of gel morphology versus concentration were constructed. The gel performance was found to depend on the HPAM concentration and the crosslinking ratio (molar ratio of HPAM carboxyl groups to Cr³⁺ ions). No gel formation occurred when the HPAM concentration was below 800 mg/L, while concentrations above 2500 mg/L effectively inhibited over-crosslinking. The crosslinking ratio range for forming SSG was 5.56 to 18.68, with an optimal value of 9.27. Furthermore, the effect of propagation distance on gelation performance was investigated through 60 m sand-packed flow experiments. Results indicated that the minimum value of the crosslinking ratio was 2.632, the stable SSG formed when the propagation distance was less than 21 m, SWG formed within the 21–34 m range, and no intact gel formed beyond 34 m. It means that only the first 35% of the designed distance formed effective SSG for plugging. Finally, an optimization method for gel dosage design was established based on the findings. This method determines the optimal gel dosage for achieving effective plugging by calculating the volume of crosslinking system passing through the target fluid diversion interface and referencing the gel morphology distribution maps. These findings provide a straightforward and effective approach for the precise design of in-depth profile control agents. Full article

Despite the availability of effective vaccines, yellow fever outbreaks persist, highlighting the need for antiviral drugs. Background/Objectives: This study investigated Hippeastrum puniceum (Amaryllidaceae) as a potential source of antiviral compounds against wild-type yellow fever virus (wt-YFV). Methods/Results: The crude bulb extract of H. puniceum exhibited 58% protection against wt-YFV. Bioassay-guided fractionation of the extract by UHPLC-HRMS led to the annotation of six alkaloids (bulbisine, cathinone, trigonelline, tetrahydroharman-3-carboxylic acid, and 2,7-dimethoxyhomolycorine or 3-O-acetylnarcissidine) in active fractions, along with the amino acids arginine, asparagine, tryptophan, and glutamic acid. In silico ADMET analyses predicted favorable pharmacokinetic and toxicological profiles, supporting their potential as drug candidates. Six of the annotated compounds were evaluated in vitro for cytotoxicity and antiviral activity against wt-YFV. However, none showed significant antiviral activity when tested individually, suggesting that the observed antiviral effect may result from synergistic interactions between two or more compounds within active fractions. Conclusions: Our results underscore the importance of further investigations in vitro, particularly assays exploring the synergy among the annotated compounds against YFV. The integration of bioassay-guided fractionation of active plant extracts with computational analyses emerges as a promising strategy for the discovery of natural products with therapeutic potential against yellow fever, a reemerging disease. Full article

The reverse water gas shift reaction (RWGS) is a key step in the valorization of CO₂ to value-added products such as fuel. Metal carbides, particularly molybdenum carbide (Mo₂C), supported on transition metal oxide supports have been reported as promising materials to be used as catalysts for the low-temperature RWGS reaction. A deeper understanding of catalyst support interactions can be greatly beneficial for the development of better and more efficient catalysts in the future. To this end, this study computationally investigated the effect of the interaction between the Mo₂C(001) surface and the MgO(001) surface on the RWGS mechanism. The RWGS mechanisms were explored at the Mo₂C/MgO interface, as well as on the bare surface of Mo₂C. While the pathway at the interface went through an associative-type mechanism and a carboxylate intermediate, the Mo₂C surface was found to go through a redox-type mechanism. Interestingly, both the kinetics and thermodynamics of each pathway were similar, suggesting that the observed differences in the CO₂ hydrogenation pathways were primarily limited by the diffusion of CO₂ across the MgO surface rather than inhibitory energetics resulting from the interplay of the Mo₂C material and MgO support. Full article

Due to the intensive cultivation of various crops, the surface soil layer is depleted. This leads to a decrease in fertility, losses of organic matter and nutrients, and an overall decrease in soil health. We aimed to investigate the role of green manure application and organic fertilization on winter fodder barley (Hordeum vulgare L., Zemela cult.) in terms of agronomic and soil parameters. The cultivation was carried out in two fields, the predecessors of which were oats–vetch green manure (field 1) or fallow (field 2). In each field, five treatments were prepared: a control without fertilization, mineral fertilization, vermicompost, mineral fertilizer + vermicompost, and biochar. The green manure incorporation led to a decrease in grain yield of barley by 10.8–20.0% depending on the treatment. A similar tendency was observed for the rest of the studied agronomic parameters (thousand-grain mass, hectolitre weight, ear number, plants per hectare). Additionally, the vermicompost application had the most substantial effect, accounting for a 20.1% increase compared to the control, while the smallest was expressed by biochar—1.6%. Nevertheless, the photosynthesis intensity was higher in treatments after green manure. The microbiome’s activity was boosted in the vermicompost treatments, while amino acids, carboxylic acids, and polymers were the most fully metabolised compounds by the soil communities. In conclusion, the type of predecessor influenced mainly grain protein, carotenoids, and chlorophyll contents, as well as microbial activities, respiration, and dehydrogenase, while the fertilization impacted primarily on soil water and organic content, total soil N, and photosynthetic pigments of barley plants. Full article

Brackish water is becoming an increasingly important resource for agricultural irrigation due to limited freshwater availability; however, concerns persist regarding its potential to degrade soil quality and reduce crop yields. This study evaluated the combined effects of irrigation water quality (brackish water, electrical conductivity (EC) of 2958 µS/cm; agricultural water, EC 796 µS/cm), soil type (agricultural soil and reclaimed desert soil), and compost treatments (no compost, mulch compost, Johnson-Su compost, and mulch compost incorporation) on soil health and chili pepper (Capsicum annuum) growth under greenhouse conditions. Compost amendments significantly improved plant height by 58–213%, root length by 35–166%, and wet biomass by 154–1400% compared to control treatments. Agricultural water maintained lower soil EC (0.553–0.870 mS/cm) than brackish water (0.751–1.104 mS/cm), while Johnson-Su compost most effectively reduced salinity impact on plant growth. Leached water analysis showed higher Na⁺, Cl⁻, and SO₄²⁻ mobility under brackish irrigation, with compost treatments enhancing nutrient retention and soil moisture by buffering salinity stress with carboxylic group and cation exchange capacity. Johnson-Su compost incorporation consistently mitigated the negative effects of brackish irrigation by reducing sodium accumulation, improving chloride mobility, and enhancing soil nitrogen dynamics. These results highlight that combining high-quality irrigation water and biologically active composts improves soil health and plant productivity, while brackish water use requires soil amendments to mitigate salinity risks. Full article

The Auxin-Regulated Gene Involved in Organ Size (ARGOS) proteins have crucial regulatory effects on organ size and responses to environmental stresses. Despite their importance, Brassica oleracea ARGOS gene members and their functions in response to abiotic stresses have not been thoroughly investigated. In this study, we identified 40 ARGOS genes via a genome wide analysis of cauliflower and two other B. oleracea morphotypes as well as Brassica rapa, Brassica nigra, and Raphanus sativus. Expression pattern analyses indicated that these genes are responsive to multiple abiotic stresses, including salinity, heat, cold, and diverse hormones. Notably, the expression of an ARGOS-like gene (BobARL2) was upregulated in cauliflower treated with 1-aminocyclopropane-1-carboxylic acid (ACC). Moreover, the overexpression of BobARL2 decreased ethylene sensitivity, resulting in less inhibition of root elongation compared to the wild-type. Additionally, the overexpression lines exhibited enhanced salt tolerance. A yeast two-hybrid assay and luciferase complementation imaging (LCI) assay confirmed that BobARL2 can interact with Reversion-to-ethylene sensitivity Like4 (BobRTL4), which negatively regulates ethylene signal transduction. These findings advance our understanding of the evolution and functional roles of ARGOS genes in cauliflower and other Brassicaceae species, particularly in relation to abiotic stress responses, while also offering valuable insights relevant to the genetic improvement and breeding of novel varieties. Full article

Plant growth-promoting bacteria (PGPBs) offer a sustainable alternative for enhancing crop productivity in low-fertility tropical soils. In this study, 30 bacterial isolates were screened in vitro for multiple PGP traits, including phosphate solubilization (from aluminum phosphate—AlPO₄ and thermophosphate), potassium release from phonolite rock, siderophore production, indole-3-acetic acid (IAA) synthesis, ACC deaminase activity, and antagonism against Fusarium spp. Statistical analysis revealed significant differences (p < 0.05) among the isolates. The most efficient isolates demonstrated a solubilization capacity ranging from 24.0 to 45.2 mg L⁻¹ for thermophosphate and 21.7 to 23.5 mg L⁻¹ for potassium from phonolite. Among them, Pseudomonas azotoformans K22 showed the highest AlPO₄ solubilization (16.6 mg L⁻¹). IAA production among the isolates varied widely, from 1.34 to 9.65 µg mL⁻¹. Furthermore, 17 isolates produced carboxylate-type siderophores, and only Pseudomonas aeruginosa SS183 exhibited ACC deaminase activity, coupled with strong antifungal activity (91% inhibition). A composite performance index identified P. azotoformans K22, E. hormaechei SS150, S. sciuri SS120, and B. cereus SS18 and SS17 as the most promising isolates. This study provides a valuable foundation for characterizing plant growth-promoting traits and identifies key candidates for future validation and the development of microbial consortia. Full article

In this study, four types of Fe₃O₄-based magnetic nanospheres were functionalized with distinct surface groups to examine how surface chemistry influences their co-transport with tetracycline (TC) in porous media. The functional groups investigated are carboxyl (−COOH), epoxy (−EPOXY), silanol (−SiOH), and amino (−NH₂). Particles bearing −COOH, −EPOXY, or −SiOH are negatively charged, facilitating their transport through porous media, whereas −NH₂-modified particles acquire a positive charge, leading to strong electrostatic attraction to the negatively charged TC and quartz sand, and consequently substantial retention with reduced mobility. Adsorption of TC onto Fe₃O₄-MNPs is predominantly chemisorptive, driven by ligand exchange and the formation of coordination complexes between the ionizable carboxyl and amino groups of TC and the surface hydroxyls of Fe₃O₄-MNPs. Additional contributions arise from electrostatic interactions, hydrogen bonding, hydrophobic effects, and cation–π interactions. Moreover, the carboxylate moiety of TC can coordinate to surface Fe centers via its oxygen atoms. Molecular dynamics simulations reveal a hierarchy of adsorption energies for TC on the differently modified surfaces: Fe₃O₄-NH₂ > Fe₃O₄-EPOXY > Fe₃O₄-COOH > Fe₃O₄-SiOH, consistent with experimental findings. The results underscore that tailoring the surface properties of engineered nanoparticles substantially modulates their environmental fate and interactions, offering insights into the potential ecological risks associated with these nanomaterials. Full article

Pineapple leaf fibers (PALFs), obtained from abundant yet underutilized pineapple leaf residues, represent a promising feedstock for producing fibrillated cellulose. In this work, cellulosic fibers were isolated and characterized by Fiber Quality Analysis (FQA), showing lengths between 0.33 and 0.47 mm and widths of 12.2 µm after organosolv pulping using ethanol and acetic acid as a catalyst, followed by hydrogen peroxide bleaching with diethylenetriaminepentaacetic acid as a chelating agent. The cellulosic fibers were then subjected to TEMPO-mediated oxidation and subsequently disintegrated by microfluidization to produce micro-/nanofibrillated cellulose (MNFC) with a carboxylate content of 0.85 and 1.00 mmol COO⁻/g, zeta potential of −41 and −53 mV, and average widths of 15 and 12 nm for unbleached and bleached nanofibrils, respectively. The nanofibrillation yields were 73% and 68% for the bleached and unbleached MNFC samples, indicating the presence of some non-fibrillated or partially fibrillated fractions. X-ray diffraction analysis confirmed preservation of cellulose type I crystalline structure, with increased crystallinity, reaching 85% in the bleached MNFC. These findings demonstrate the feasibility of a sequential process, combining organosolv pulping, hydrogen peroxide bleaching, TEMPO-mediated oxidation, and microfluidization, for preparing MNFC from pineapple leaf fibers. Overall, this study highlights pineapple leaf residues as a sustainable source of MNFC, supporting strategies to transform agricultural waste into valuable bio-based materials. Full article

Waste materials have emerged as attractive low-cost feedstocks for adsorbent development in environmental remediation and materials engineering. Organic wastes are particularly rich in cellulose, hemicellulose, lignin, and pectin, which provide reactive oxygenated groups such as hydroxyls and carboxyls. While inorganic wastes offer stability, lower water retention makes them promising candidates. This study explores the functionalization of waste-derived organic and inorganic matrices using two amine-based agents: 3-aminopropyltrimethoxysilane (APTMS) and polyethylenimine (PEI). The materials were categorized as organic (orange peel, corn cob) or inorganic (silica gel, eggshell) and subjected to a pretreatment process involving drying, grinding, and sieving; inorganic substrates additionally underwent acid activation with citric acid. Surface modification was carried out in ethanolic (APTMS) or aqueous (PEI) media. To assess their suitability and processability as particulate sorbents, drying kinetics, physicochemical properties (FTIR, ζ-potential, pH, conductivity, Boehm titration), and flow characteristics (Carr and Hausner indices) were evaluated. The findings enable a comparative analysis of the functionalization efficiency and elucidate the relationship between substrate type (organic vs. inorganic) and its performance as a modified adsorbent. This approach advances the development of novel sorbent matrices for greenhouse gas mitigation while reinforcing circular economy principles through the valorization of low-cost, readily available waste materials. Full article

The present work is aimed at shedding light on the evolution of surface chemistry of a commercial activated carbon (AC) support during the preparation of supported metal oxide (MO) catalysts by the conventional wet impregnation method. Particular attention is paid to the chemical changes of oxygen-containing surface functionalities across three preparation stages of impregnation, oven-drying, and thermal treatment. AC was impregnated with aqueous solutions of several MO precursors (Al(NO₃)₃, Fe(NO₃)₃, Zn(NO₃)₂, SnCl₂, and Na₂WO₄) at 80 °C for 5 h, oven-dried at 120 °C for 24 h, and heat-treated at 200 °C and 850 °C for 2 h under an inert atmosphere. The surface chemistry of the resulting catalyst samples, classified in three series by the thermal treatment, was mainly studied by FT-IR spectroscopy, complemented by elemental analysis and pH of the point of zero charge (pH_pzc) measurements. During impregnation, phenolic hydroxyl and carboxylic acid groups were predominantly formed by wet oxidation of chromene, 2-pyrone, and ether-type structures found in the pristine AC. The extent of these oxidations correlated with the oxidising power of the precursor solutions. As expected, thermal treatment at 850 °C brought about markedly stronger chemical changes, with most of the above oxygen functionalities decomposing and forming less acidic structures, such as 4-pyrone groups, metal carboxylates, and C-O-M atomic groupings. All these surface chemical modifications result in a lowering of the strong basicity of the raw carbon support (pH_pzc ≈ 10.5), thus leading to pH_pzc values for the catalysts widely ranging from 1.6 to 9.7. Full article

The terpeno-heterocyclic molecular hybrids are a new and promising class of modern organic and medicinal chemistry, because their molecules exhibit high and selective biological activity, natural origins, and good biocompatibility, and, usually, they are less toxic. The reported norlabdane-heterocyclic hybrids were synthesized by classical and new, original, and environmentally friendly methods, which include coupling reactions of norlabdane derivatives (such as carboxylic acids, acyl chlorides, or bromides) with individual heterocyclic compounds, as well as heterocyclization reactions of certain norlabdane intermediates like hydrazides, thiosemicarbazones, or hydrazinecarbothioamides. The aforementioned norlabdanes were derived from (+)-sclareolide 2, which is readily obtained from (−)-sclareol 1, a labdane-type diterpenoid extracted from the waste biomass of Clary sage (Salvia sclarea L.) that remains after essential oil extraction. All synthesized compounds were tested against various fungal strains and bacterial species, with many exhibiting significant antifungal and antibacterial activity. These findings support the potential application of the synthesized compounds in the treatment of diseases caused by fungi and bacteria. Additionally, the use of plant-based waste materials as starting resources highlights the economic and ecological value of this approach. This review summarizes experimental data on the synthesis and biological activity of norlabdane: diazine, 1,2,4-triazole and carbazole, 1,3,4-oxadiazole, 1,3,4-thiadiazole, 1,3-thiazole, 1,3-benzothiazole and 1,3-benzimidazole hybrids performed by our research group covering the period from 2013 to the present. Full article

With the development of the new energy industry in high-altitude regions, epoxy resin insulating materials in electrical equipment face severe challenges from prolonged exposure to strong radiation environments. Strong ultraviolet irradiation induces the generation of free radicals such as alkyl (CH₂), alkoxy (CH₂O), and peroxyl (CH₂OO), which continuously attack the cross-linking structure of epoxy resin, leading to its degradation. This study employs molecular dynamics simulations to evaluate the enhancing effect of graphene quantum dots (GQDs) on the radiation resistance of epoxy resin (EP), proposing cross-linking structural integrity as an evaluation criterion. It compares and analyses pure EP (EP/neat), hydrogen-terminated GQDs (EP/GQD_C₅₄H₁₈), and carboxyl-terminated GQDs (EP/GQD_COOH) under three types of free radicals. The results indicate that the unique sp² hybrid structure and hydrogen-donating ability of GQDs can effectively inhibit the activity of free radicals, and improve the integrity of the cross-linked structure by 8% to 16% compared to EP/neat. While both types of GQDs demonstrate comparable behavior in response to alkyl free radicals, EP/GQD_COOH exhibits superior performance under the influence of oxygen-containing free radicals. This enhanced performance can be attributed to its augmented hydrogen-donating capacity and an increased number of active sites. This study investigates the extent to which GQDs with different structures enhance the radiation resistance of epoxy resins, providing an important theoretical basis for the modification of epoxy resins for applications in high-radiation environments. Full article