Search Results (20,695)

Pineapple biomass represents an abundant renewable source of carbon and a promising feedstock with considerable potential for the production of sustainable fuels. In the present study, the influence of liquid hot water (LHW) pretreatment on the pineapple mother plant was investigated at different controlled severities, then characterized by Fourier-transform infrared spectroscopy (FTIR), X-ray diffraction (XRD), thermogravimetric analysis (TGA), and scanning electron microscopy (SEM). Results show that LHW pretreatment causes structural changes, leading to lignin and hemicellulose depolymerization up to a severity factor of 2.36–3.55, whereas at severity factors in the range of 4.13–5.90, cellulose, hemicellulose, and lignin appear to repolymerize. This pretreatment resulted in a higher hydrolysis efficiency (94.92 ± 0.04%) at 50 °C for 72 h. Compared with the untreated sample, the hydrolysis rate under these conditions increased by a factor of 2.16. SEM imaging revealed significant disruption of the PMP microstructure following LHW treatment, while XRD data confirmed an increase in the crystallinity index. FTIR analysis further indicated modifications in functional group profiles, supporting the structural and compositional changes induced by pretreatment. Overall, this study demonstrates the effectiveness of LHW pretreatment in enhancing the enzymatic digestibility and modifying the physicochemical properties of PMP biomass, providing a foundation for its valorization into high value bioproducts. Full article

This study aims to enhance the oxidative stability of fish oil through encapsulation in pullulan/sodium caseinate (PUL/NaCAS) nanofibers. Electrospinning was employed to produce three formulations: control (0% fish oil) and samples with 5% and 10% fish oil. Characterization of the emulsions showed that increasing oil content led to larger droplet size and reduced viscosity. Scanning electron microscopy (SEM) analysis revealed surface imperfections and a gradual increase in fiber diameter with higher oil loading. Fourier transform infrared (FTIR) spectroscopy confirmed molecular interactions, and fibers with 10% fish oil showed a shift toward a more amorphous structure. Fish oil incorporation also enhanced hydrophobicity and thermal stability, as indicated by thermal and wettability measurements. Antioxidant assays include 2,2-diphenyl-1-picrylhydrazyl (DPPH), 2,2′-azino-bis (3-ethylbenzothiazoline-6-sulfonic acid) (ABTS), and total phenolic content (TPC), which showed the highest bioactivity at 5% fish oil, with a slight decrease at 10%, likely due to structural saturation. Encapsulation at 5% fish oil significantly reduced lipid oxidation during storage (hydroperoxide values decreased from 8.6 to 4.8 mM at 60 °C/15 days), demonstrating the protective effect of the nanofiber matrix. Docking and density functional theory (DFT) analyses confirmed stable DHA/EPA–caseinate interactions and increased electronic stability, supporting the experimental results. Compared with conventional carriers such as spray-dried or maltodextrin-based systems, PUL/NaCAS nanofibers offered superior oxidative stability, bioactivity, and a biodegradable matrix. Overall, the 80PUL:20NaCAS:5% fish oil formulation represents a versatile platform for stabilizing omega-3 oils, with potential applications in food preservation, nutraceutical delivery, and functional packaging. Full article

Tin slags generated during cassiterite smelting in Brazil contain significant amounts of technologically important metals such as niobium, tantalum, and zirconium. Improper disposal of these materials represents both an environmental concern and the loss of a valuable secondary source of critical elements. This study aimed to characterize a Brazilian tin slag sample to evaluate its composition, morphology, and potential for metal recovery. The material was homogenized and analyzed by laser diffraction (particle size), ICP-OES (chemical composition), X-ray diffraction (mineral phases), differential scanning calorimetry (metallic tin), and scanning electron microscopy with energy-dispersive spectroscopy (morphology). The slag exhibited a heterogeneous particle size distribution (D90 = 0.75 mm, D50 = 0.30 mm, D10 = 0.09 mm) and a complex multiphase structure composed mainly of silica, calcium silicate, and zirconia. The chemical analysis revealed 4.8 wt% Nb and 0.8 wt% Ta, along with high concentrations of Zr (11.1 wt%), confirming the material’s potential as a secondary resource. Thorium (2.7 wt%) and uranium (0.3 wt%) were also detected, indicating the presence of radioactive constituents. The detailed characterization of the slag provides essential insights into its chemical and mineralogical complexity, which directly influence the selection of suitable recovery routes. Understanding the distribution of Nb- and Ta-bearing phases within the refractory silicate–zirconia matrix is fundamental for defining pretreatment and leaching strategies. Therefore, this study establishes a necessary foundation for the design of efficient hydrometallurgical processes aimed at recovering critical metals from Brazilian tin slags. Full article

Early pest detection in edible crops demands sensing solutions that can run at the edge under tight power, budget, and maintenance constraints. This review synthesizes peer-reviewed work (2015–2025) on three modality families—vision/AI, spectroscopy/imaging spectroscopy, and indirect sensors—restricted to edible crops and studies reporting some implementation or testing (n = 178; IEEE Xplore and Scopus). Each article was scored with a modality-aware performance–cost–implementability (PCI) rubric using category-specific weights, and the inter-reviewer reliability was quantified with weighted Cohen’s $\kappa$. We translated the evidence into compact decision maps for common deployment profiles (low-power rapid rollout; high-accuracy cost-flexible; and block-scale scouting). Across the corpus, vision/AI and well-engineered sensor systems more often reached deployment-leaning PCI (≥3.5: 32.0% and 33.3%, respectively) than spectroscopy (18.2%); the median PCI was 3.20 (AI), 3.17 (sensors), and 2.60 (spectroscopy). A Pareto analysis highlighted detector/attention models near $(P,C,I)\approx (4,5,4)$; sensor nodes spanning balanced $(4,4,4)$ and ultra-lean $(2,5,4)$ trade-offs; and the spectroscopy split between the early-warning strength $(5,4,3)$ and portability $(4,3,4)$. The inter-rater agreement was substantial for sensors and spectroscopy (pooled quadratic $\kappa$ = 0.73–0.83; up to 0.93 by dimension) and modest for imaging/AI (PA vs. Author 2: ${\kappa }_{\mathrm{quadratic}}=0.30$–$0.44$), supporting rubric stability with adjacency-dominated disagreements. The decision maps operationalize these findings, helping practitioners select a fit-for-purpose modality and encouraging a minimum PCI metadata set to enable reproducible, deployment-oriented comparisons. Full article

As a chitosan (CTS)-based drug carrier (DC) for doxorubicin (DOX) delivery, poly(2-hydroxyethyl methacrylate-co-2-hydroxy-4-N-methacrylamidobenzoic acid) [poly(HEMA-co-2-HMBA)] (PHCH) was successfully grafted onto chitosan to fabricate DOX-loaded microparticles, and their in vitro release behavior was systematicaly investigated. Morphological characteristics were analyzed using scanning electron microscopy (SEM) and transmission electron microscopy (TEM), while DOX loading was validated through Fourier-transform infrared (FTIR) spectroscopy and thermogravimetric analysis (TGA), comparing pure and drug-loaded microparticles. The maximum loading capacity (~91%) was attributed to the presence of abundant carboxylic acid groups, which imparted pH responsiveness during in vitro DOX release. Furthermore, density functional theory (DFT) calculations revealed that hydrogen bonding interactions between DOX and the functional groups of the microparticles strongly influenced encapsulation efficiency (EE%), drug loading (DL%), and release behavior. The fabricated microparticles exhibited pH-dependent DOX release, with accelerated and more complete release at tumor microenvironment pH 5.5 compared to physiological pH 7.4. These results demonstrate that PHCH grafted CTS microparticles are promising candidates for controlled and site-specific anticancer drug delivery. Full article

The oxygen reduction reaction (ORR) is a crucial process in electrochemical systems, such as fuel cells, as it effectively converts oxygen into water, thereby contributing significantly to sustainable energy generation. In this study, copper oxide (CuO) thin films were deposited onto silver (Ag) substrates using a modified successive ionic layer adsorption and reaction (SILAR) method, followed by an investigation of their electrocatalytic performance toward ORR in an alkaline medium. Comprehensive electrochemical characterizations, including cyclic voltammetry (CV), electrochemical impedance spectroscopy (EIS), and open circuit potential (OCP), were employed to evaluate catalyst behaviour. Elemental analysis through energy-dispersive X-ray spectroscopy (EDX) confirmed the uniform distribution of CuO, while scanning electron microscopy (SEM) revealed a sponge-like surface morphology which potentially enhances catalytic efficiency. Moreover, EIS spectra revealed a lower charge transfer resistance for the CuO/Ag electrode (3.37 kΩ) compared to bare Ag (4.23 kΩ), reflecting improved ORR kinetics. Among different deposition cycles, 15 SILAR cycles yielded the highest current density of 0.8 mA cm⁻² at 0.60 V. Kinetic analysis revealed that the reaction is irreversible, with a lower value of Tafel slope (32 mV dec⁻¹) and high transfer coefficient (α = 0.45), indicating a concerted reduction mechanism. The ORR pathway was found to follow a four-electron (4e⁻) transfer process. Full article

This study synthesized a low-molecular-weight donkey-hide gelatin peptide–zinc chelate (LMW DHGP–Zn) using peptides derived from donkey-hide gelatin. Under optimized conditions (zinc concentration of 32 mg/mL, peptide-to-zinc mass ratio of 8:1, pH 6.5, 60 °C, 70 min), a maximum chelation rate of 41.34% ± 0.23% was achieved. Comprehensive characterization via scanning electron microscopy, ultraviolet–visible spectroscopy, fluorescence spectroscopy, zeta potential, particle size, Fourier transform infrared spectroscopy, and circular dichroism confirmed substantial structural and physicochemical alterations post-chelation. After chelation, the surface charge is neutralized, and the distribution of particles is more even. Furthermore, analysis indicated an elevated content of acidic amino acids (glutamic acid and aspartic acid), and spectroscopic data confirmed the coordination of zinc ions with amino and carboxyl groups on the peptide. Consequently, the LMW DHGP–Zn chelate demonstrated significantly enhanced ABTS radical cation scavenging activity. These results provide a scientific foundation for its potential application as a natural antioxidant in the food, cosmetic, and pharmaceutical industries. Full article

High Mobility Group Box 1 (HMGB1) is a central pro-inflammatory mediator released from damaged or stressed cells, where it activates receptors such as the Receptor for Advanced Glycation Endproducts (RAGE). Dendritic polyglycerol sulfate (dPGS), a hyperbranched polyanionic polymer, is known for its anti-inflammatory activity. In this study, we examined how dPGS modulates HMGB1-driven signaling in RAW 264.7 macrophages and human microglia. Recombinant human HMGB1 expressed in Escherichia coli (E. coli) was purified by nickel-nitrilotriacetic acid (Ni-NTA) and heparin chromatography. Proximity ligation assays (PLA) revealed that dPGS significantly disrupted HMGB1/RAGE interactions, particularly under lipopolysaccharide (LPS) stimulation, thereby reducing inflammatory signaling complex formation. This correlated with reduced activation of the nuclear factor kappa B (NF-κB) pathway, demonstrated by decreased nuclear translocation and transcriptional activity. Reverse transcription polymerase chain reaction (RT-PCR) and quantitative real-time PCR (RT-qPCR) showed that dPGS suppressed HMGB1- and LPS-induced transcription of tumor necrosis factor alpha (TNF-α), interleukin-6 (IL-6), monocyte chemoattractant protein-1 (MCP-1), cyclooxygenase-2 (COX-2), and inducible nitric oxide synthase (iNOS). Enzyme-linked immunosorbent assay (ELISA) and Griess assays confirmed reduced TNF-α secretion and nitric oxide production. Electron paramagnetic resonance (EPR) spectroscopy further showed that dPGS altered HMGB1/soluble RAGE (sRAGE) complex dynamics, providing mechanistic insight into its receptor-disruptive action. Full article

Dielectric barrier discharge (DBD) was used as a source of low-temperature plasma generated in a mixture of air and argon at atmospheric pressure for the deposition of a TiO₂ layer from a precursor on a brass or glass substrate. The DBD was generated between two plane-parallel electrodes covered with a dielectric barrier and supplied with an AC high voltage at a frequency of 5 kHz. In this paper, a TiO₂ layer was deposited from vaporised titanium tetraisopropoxide (TTIP), as a precursor, conveyed via argon as a carrier gas in air. The deposited layer was then annealed at a temperature of 450 °C for a time of 2 h. The results of laboratory investigations show that DBD plasma generated in a mixture of air and argon at atmospheric pressure with a precursor can be a useful tool to produce an anatase TiO₂ thin porous layer. The physical properties of the obtained layers were characterised by scanning electron microscopy, energy-dispersive spectroscopy, and Raman spectroscopy. Layer morphology was different depending on the substrate used: in the case of the brass substrate, the layer was built from particles with an average size larger than that of the layer built on the glass substrate. The effect of substrates with different electrical properties on TiO₂ layer morphology deposited in DBD has not yet been investigated. Full article

High density alumina–zirconia–tantalum ceramic–metal composites with the addition of 0.5 vol.% of graphene oxide were fabricated via a wet processing technique followed by spark plasma sintering. Scanning electron microscopy confirmed the even distribution of metal particles in the composite matrix. The thermal reduction of graphene oxide after consolidation at 1500 °C was proved using Raman spectroscopy. The engineered materials exhibit a fracture resistance of 16 MPa∙m^1/2, which is 30% greater than in the reference ZTA ceramic composites fabricated using the same technology. That increase in fracture toughness could be down to a synergetic interaction mechanism; more specifically, crack trapping, renucleation and blunting, and elongated tantalum particles bridging. In addition to the above-mentioned mechanisms, tetragonal monoclinic phase transformation in zirconia is also an additional source of increased crack resistance in the developed composites. Full article

Forging plays a crucial role in various industries, including aerospace, automotive, oil and gas, and defense. We investigated the effect of post-processing forging on microstructural and mechanical properties of 316L stainless steel forging preforms fabricated by laser powder bed fusion. The as-built samples were subjected to hot forging in order to refine the microstructure and enhance mechanical performance. Detailed characterization was performed using Electron Backscatter Diffraction, Scanning Electron Microscopy, Energy Dispersive Spectroscopy, Tensile testing, and Hardness Testing. Substantial grain refinement (up to 97%) was observed, in addition to a reduction in porosity. The forging process effectively transformed the columnar grain morphology into equiaxed grains, increased yield and ultimate tensile strengths of 560 MPa and 740 MPa, representing 27% and 32% improvements, respectively, with a corresponding decrease in elongation to 32% from 47%. The horizontally built samples achieved the highest yield strength of 605 MPa but slightly lower UTS 710 MPa, representing 32% and 5% increment and decrease in ductility to 28% from 37.5%. These trends reflect the combined effects of work hardening and grain refinement, which enhance strength at the expense of ductility. Full article

The application of laser powder bed fusion (LPBF) to 7xxx-series aluminum alloys is fundamentally limited by hot cracking and porosity. This study demonstrates that adding 5 wt.% AlCoCrFeNi_2.1 high-entropy alloy (HEA) particles to 7075 aluminum alloy (AA7075) powder can effectively mitigate these issues. Microstructural characterization revealed that the HEA particles remained largely intact and formed a strong metallurgical bond with the α-Al matrix. Scanning electron microscopy (SEM) and energy-dispersive X-ray spectroscopy (EDS) analysis confirmed that this bonding is facilitated via the in situ formation of new intermetallic phases at the particle/matrix interface. X-ray diffraction (XRD) identified these phases as primarily Al₅Co₂ and Fe₃Ni₂. A key consequence of this reinforced interface is a significant change in cracking behavior; optical microscopy (OM) showed that long, continuous cracks typical of AA7075 were replaced by shorter, deflected cracks in the composite. While porosity was not eliminated, the addition of HEA stabilized the process, yielding a consistent density improvement of 0.5–1.5% across the processing window. This microstructural modification resulted in a substantial ~64% increase in average microhardness, which increased from 96.41 ± 9.81 HV_0.5 to 158.46 ± 11.33 HV_0.5. These results indicate that HEA reinforcement is a promising route for engineering the microstructure and improving the LPBF processability of high-strength aluminum alloys. Full article

Perfluorooctanesulfonate (PFOS) is a typical persistent organic pollutant, which presents a significant risk to the ecosystem and human health. Therefore, the development of a highly sensitive and effective detection technique for PFOS has aroused wide concern. In this study, for the mesoporous metal–organic frameworks (MOFs), Cr-MIL-101 were used as the precursor. And the poly(3,4-ethylenedioxythiophene) (PEDOT) using as molecularly imprinted polymers (MIPs) was loaded on Cr-MIL-101 to form a core–shell structure. The obtained Cr-MIL-101@PEDOT/MIP composites integrate the high specific surface area of Cr-MIL-101 and the specific recognition capability of PEDOT/MIP. The glassy carbon electrode (GCE) interface modified by them can specifically adsorb PFOS through electrostatic interactions, coordination by Cr metal nodes, hydrophobic interaction, and hydrogen bonding, etc. The adsorbed PFOS molecules could block the active sites at the electrode interface, causing the current decay of the redox probe. Following the quantitative analysis of peak current decay values using the Langmuir model and the Freundlich–Langmuir model, a wide detection range (0.1–200 nM) and a low detection limit (0.025 nM) were obtained. Characterization techniques including scanning electron microscopy (SEM), transmission electron microscopy (TEM), X-ray diffraction (XRD), Brunauer–Emmett–Teller (BET), X-ray photoelectron spectroscopy (XPS), and electrochemical methods were employed to validate the fabrication of the composites. Moreover, Cr-MIL-101@PEDOT/MIP/GCE showed satisfactory stability, repeatability, and selectivity, providing an effective method for the detection of PFOS in practical samples, showing a wide prospective application. Full article

The Qianlong Tripitaka preserved in the Capital Museum is a distinctive large-scale wood block printing plates of the Qing Dynasty. It represents a unique type of Chinese documentary wooden heritage preserved in a dry museum environment, which has rarely been subjected to comprehensive physicochemical analysis, resulting in an inadequate understanding of their deterioration processes. This study applied a comprehensive multi-analytical method to investigate the deterioration of the scripture plates. The findings indicate that the Qianlong Tripitaka shows typical structural deformation, chemical depolymerization, and a decline in structural integrity and stability. Scanning Electron Microscopy (SEM) and Computed Tomography (CT) revealed thinning and the distortion of cell walls, reduced density, and partial collapse of tissue structures. Thermogravimetric Analysis (TGA) indicated lower decomposition temperatures and higher inorganic residues, while a Brunauer–Emmett–Teller surface area analyzer (BET) showed diminished surface area, expanded pores, and compromised connectivity. Moisture content analyses verified significant water loss, contributing to brittleness and susceptibility to microbial degradation. Fourier Transform Infrared Spectroscopy (FTIR) and X-ray Diffraction (XRD) analyses revealed considerable hemicellulose degradation, the disruption of cellulose crystallinity, and relatively stable lignin. This study highlights the value of a multi-analytical strategy for assessing the deterioration of wooden cultural heritage, providing a transferable framework for similar documentary wooden artifacts. Full article

This article reports on the synthesis and physicochemical characterization of a novel complex ferrite material, LiCr₃.₄Fe₁.₆O₈, prepared via the sol-gel method. X-ray diffraction (XRD) analysis confirmed that the synthesized compound is a single-phase material with a spinel-type structure and cubic symmetry. Raman spectroscopy was employed to investigate the vibrational modes, and the observed peaks corresponding to Fe–O and Cr–O bonds further validated the spinel-like structure of the compound. The microstructure and elemental composition were examined using scanning electron microscopy (SEM). Multiple regions of the LiCr₃.₄Fe₁.₆O₈ crystals were analyzed, revealing a homogeneous phase and providing detailed insight into the morphology and chemical composition of the surface. The synthesized ferrite particles exhibited relatively large dimensions, with sizes measured at approximately 5, 30, 100, and 200 μm. The dielectric behavior was studied to assess the material’s response to an external electric field, demonstrating its capacity for electric charge polarization. Both capacitance and electrical conductivity were found to increase with rising temperature. Electrophysical measurements were conducted using the LCR-800 system over a temperature range of 293–483 K and at frequencies of 1.5 kHz and 10 kHz. An increase in frequency to 10 kHz resulted in a decrease in the dielectric constant (ε) across the entire temperature range. Full article