Search Results (140)

The compliant discharge of landfill leachate constitutes a pivotal factor for the effective implementation of integrated water resource management. Aged landfill leachate exhibits complex composition and an imbalanced carbon-to-nitrogen ratio. Electrocatalytic oxidation technology, as an efficient advanced oxidation process, demonstrates promising application potential. This study employed Ti/RuO₂–IrO₂ Anodes for the electrocatalytic oxidation treatment of aged landfill leachate. The removal efficiencies and variation patterns of chemical oxygen demand (COD), ammonia nitrogen, and total nitrogen at different current densities and reaction times were systematically investigated, along with an analysis of energy consumption and current efficiency. The degradation and transformation processes of organic matter were elucidated using Three-dimensional Excitation–Emission Matrix (EEM) Spectra. Fresh anodes and those used for 1000 h were characterized by scanning electron microscopy (SEM) and energy-dispersive spectroscopy (EDS) to elucidate their failure mechanisms. The results demonstrate that electrocatalytic oxidation achieves efficient pollutant removal. At a current density of 1000 A/m² and a reaction time of 30 min, the effluent concentrations of ammonia nitrogen and total nitrogen satisfied the discharge standards, while COD complied with emission requirements after 60 min. The pollutant removal efficiencies were positively correlated with current density and reaction time. EEM analysis revealed that the electrocatalytic process effectively disrupts the structure of macromolecular organic matter, degrading it into smaller molecules and eventually achieving complete mineralization. Electrode characterization identified titanium substrate corrosion due to coating cracks and coating detachment as the primary causes of electrode failure. This study confirms the effectiveness of electrocatalytic oxidation technology for treating aged landfill leachate, and provides a theoretical foundation and technical support for its practical engineering application. The technology exhibits considerable theoretical significance and promising application potential in the treatment of landfill leachate. Full article

Yam polysaccharides are promising functional food ingredients, but the systematic understanding of how cultivar and processing synergistically determine their structure and functionality is still lacking. This study systematically investigated how hot water extraction, enzymatic hydrolysis, and extrusion puffing affect the structural and functional properties of polysaccharides from two major cultivars (Dioscorea opposite cv. Tiegun and Dioscorea esculenta cv. Gaozhou). Enzymatic extraction increased yield (1.39–1.77-fold) and solubility, while hot water extraction favored purity. The monosaccharide composition was strongly cultivar-dependent, with Tiegun polysaccharides containing higher mannose levels. Extrusion puffing of Gaozhou polysaccharide improved solubility by 33.3% but induced depolymerization and aggregation, modifying colloidal and functional behaviors. Multivariate analysis revealed that processing methods primarily governed macromolecular architecture and colloidal properties, whereas cultivar determined chemical composition. These findings establish a processing–structure–property framework, enabling the tailored production of yam polysaccharides: Tiegun yam with enzymatic extraction for high bioactivity, and Gaozhou yam with extrusion puffing for superior solubility. Full article

This study investigates the dynamic behavior and structural optimization of hydraulic water well drilling rig masts through a comparative finite element analysis (FEA) of metallic and composite configurations. The reference model, manufactured from structural steel (S355J2/E315), was compared with two optimized lightweight alternatives made of carbon fiber reinforced polymer (CFRP) and glass fiber reinforced polymer (GFRP) laminates. Simulations were performed in MSC Visual Nastran using identical geometric and loading conditions, including the critical dynamic event of drill string pull-out. The results demonstrate that substituting steel with composite materials significantly decreases the overall mass by up to 55%, while increasing the first natural frequency by 20–25% and reducing dynamic stress amplification by approximately 15–20%. Furthermore, the maximum tip displacement of the mast was reduced by 35–45% for the composite variants, indicating improved stiffness and vibration damping capability. These findings confirm that polymer composite structures offer superior dynamic performance, lower inertial loads, and enhanced operational safety, providing a viable route for next-generation lightweight drilling rig designs integrating advanced macromolecular materials. Full article

Rising concentrations of organic carbon (OC), phosphorus, and nitrogen in liquid waste from urban, industrial, and agricultural sources pose persistent challenges for environmental protection and resource recovery. Despite extensive application of microfiltration (MF) and ultrafiltration (UF) in wastewater treatment, their role in selective organic carbon and nutrient fractionation remains insufficiently clear-cut and is often interpreted solely through nominal pore size. This review was guided by the hypothesis that the reported limitations of MF and UF for nutrient separation are not intrinsic to the technologies but arise from simplified interpretations of separation mechanisms. A unified analytical framework was developed by synthesizing recent studies, linking membrane surface charge, pore structure, solute speciation, fouling-induced secondary layers, and operating conditions to the observed separation behavior. The analysis shows that MF fractionates particulate OC and suspended solids, whereas UF extends separation to macromolecular OC and phosphorus mainly via indirect retention mechanisms. Dissolved nitrogen species largely permeate both membranes unless they are transformed into retainable forms. Performance differences between MF and UF are conditional and system-dependent, with enhanced selectivity emerging through process integration. MF and UF can thus be repositioned as strategic fractionation interfaces within integrated treatment systems supporting circular economy–oriented wastewater management. Full article

Stabilizing thermoplastic polymers against thermal degradation is an important aspect that must be addressed during material development and becomes critical in the case of bio-polymers, which often reveal reduced thermal stability and a narrow processing temperature window. Herein, we propose a new methodology to analyze and compare the thermal stability of thermoplastic materials, exampled by several types of bio-polyesters, such as aliphatic PBS and PBSA, aliphatic-aromatic PBAT and PBST, and amorphous PHBV, and evaluate the impact of thermal stabilizer on their processability and thermal stability. The proposed method relies on multi-step torque rheometry experiments that involve controlled cycling of the tested material under varied thermal conditions, shear forces, and processing times to acquire and evaluate the changes in flow behavior of the sample after its processing. By monitoring polymer melt behavior and comparing the changes before and after repetitive processing steps, we can gain valuable insights into the material performance and stabilizing efficiency of additives. The thermal stability of polymers and the efficiency of thermal stabilizers can be assessed by means of the relative change in temperature-normalized torque, $∆\tau \left(\%\right)$, measured after different processing steps. Significantly, we demonstrate that the obtained $∆\tau \left(\%\right)$ values correlate with changes in the molar mass of neat polymers as a result of their processing. The proposed approach enables a semi-quantitative evaluation of the thermal stability of various polymers and the study of the efficiency of thermal stabilizers and their performance, providing a robust strategy for optimizing compound formulations, particularly regarding the optimal fractions required. Full article

The widespread use of antibiotics, combined with pervasive exposure to diverse environmental media, has intensified the global challenge of antibiotic resistance. Accumulating evidence reveals that beyond direct antibiotic pressure, residual non-antibiotic chemicals—despite lacking intrinsic antibacterial activity—can significantly promote the enrichment and spread of antibiotic resistance genes (ARGs) in farmland soils through indirect mechanisms such as inducing oxidative stress, altering microbial community structure, and enhancing both vertical and horizontal gene transfer. To address this issue, the present study investigates the influence of representative non-antibiotic contaminants commonly detected in agricultural environments—including pesticides (e.g., Omethoate, imidacloprid, and atrazine), industrial pollutants (e.g., PCB138, BDE47, benzo [a] pyrene, 2,3,7,8-tetrachlorodibenzo-p-dioxin [TCDD], and benzene), plastic-associated compounds (e.g., Polyethylene trimer, phthalates, and tributyl acetylcitrate), and ingredients from personal care products (e.g., triclosan and bisphenol A)—on ARG transmission dynamics. Leveraging bioinformatics resources such as the CARD database, PDB, AlphaFold, and molecular sequence analysis tools, we identified relevant small-molecule ligands and macromolecular receptors to construct a simulation system modeling ARG transfer pathways. Molecular docking and molecular dynamics (MD) simulations were then implemented, guided by a Plackett–Burman experimental design, to systematically evaluate the impact of individual and co-occurring pollutants. The resulting data were processed using advanced analytical tools, and MD trajectories were interpreted at the molecular level across three scenarios: an unperturbed (blank) system, single-pollutant exposures, and dual-pollutant combinations. By integrating computational simulations with machine learning approaches, this work uncovers the “co-selection” effect exerted by non-antibiotic chemical residues in shaping the environmental resistome, thereby providing a mechanistic and scientific basis for comprehensive risk assessment of agricultural non-point source pollution and the development of effective soil health management and antimicrobial resistance containment strategies. Full article

Alzheimer’s disease (AD) is considered one of the leading causes of death in the United States, and there is no effective cure for it. Understanding the neuropathological mechanisms underlying AD is essential for identifying early, reliable biomarkers and developing effective therapies. In this paper, we report on a comprehensive multimodal study of AD pathology using the 5xFAD mouse model. We employed light-scattering techniques, Partial Wave Spectroscopy (PWS) and Inverse Participation Ratio (IPR), to detect nanoscale structural alterations in brain tissues, nuclear components, and mitochondria. To support the light-scattering experiments, behavior, and histopathological studies were conducted. These analyses revealed significant increases in structural heterogeneity and mass density fluctuations in the brains of 5xFAD mice compared with Non-transgenic controls. Behavioral assessment performed using the Novel Object Recognition test demonstrated memory impairment in 5xFAD mice, reflected by a reduced recognition index. Histopathological analysis further revealed increased amyloid beta plaques and microglia activation in the hippocampus and cortex of 5xFAD mice compared with Non-transgenic controls. An increase in structural disorder within brain tissues can be attributed to higher mass density fluctuations, likely arising from macromolecular rearrangement driven by amyloid beta aggregation and neuroinflammatory responses as the disease progresses. Our findings suggest that PWS and IPR-derived metrics provide sensitive biophysical indicators of early cellular and subcellular disruption, offering potential as quantitative biomarkers for the detection of AD. Full article

The emergence of electrically conductive polymeric materials has revolutionized the landscape of sustainable energy technologies, presenting unprecedented opportunities for advancing both photovoltaic conversion systems and electrochemical energy-storage platforms. These remarkable macromolecular materials exhibit distinctive characteristics including adjustable electronic band structures, exceptional mechanical adaptability, solution-phase processability, and cost-effective manufacturing potential. This extensive review provides an in-depth examination of the fundamental principles governing charge carrier mobility in conjugated polymer systems, explores diverse synthetic methodologies for tailoring molecular architectures, and analyzes their transformative applications across multiple energy technology domains. In photovoltaic technologies, electrically conductive polymers have driven major advancements in organic solar cells and photoelectrochemical systems, significantly improving energy conversion efficiency while reducing manufacturing costs. In electrochemical energy storage, their integration into supercapacitors and rechargeable lithium-based batteries has enhanced charge storage capability, accelerated charge–discharge processes, and extended operational lifespan compared with conventional electrode materials. This comprehensive analysis emphasizes emerging developments in hybrid composite architectures that combine conductive polymers with carbon-based nanomaterials, metal oxides, and other functional components to create next-generation flexible, lightweight, and wearable energy systems. By synthesizing fundamental materials chemistry with device engineering perspectives, this review illuminates the transformative potential of electrically conductive polymers in establishing sustainable, efficient, and resilient energy infrastructures for future technological landscapes. Full article

Determining the postmortem interval remains one of the most persistent and fragmented challenges in forensic science. Conventional approaches—thermal, biochemical, molecular, or entomological—capture only isolated fragments of a single physical reality: the irreversible drift of a once-living system toward equilibrium. This Perspective proposes a unifying paradigm in which death is understood as a progressive rise in entropy, encompassing the loss of biological order across thermal, chemical, structural, and ecological domains. Each measurable postmortem variable—temperature decay, metabolite diffusion, macromolecular breakdown, tissue disorganization, and microbial succession—represents a distinct expression of the same universal law. Within this framework, entropy becomes a dimensionless index of disorder that can be normalized and compared across scales, transforming scattered empirical data into a coherent continuum. A Bayesian formulation further integrates these entropic signals according to their temporal reliability, yielding a probabilistic, multidomain equation for PMI estimation. By merging thermodynamics, information theory, and biology, the concept of death as rising entropy offers a comprehensive physical description of the postmortem process and a theoretical foundation for future computational, imaging, and metabolomic models in forensic time analysis. Full article

The present work consisted of a comparative analysis, followed by an extensive narrative literature review, of the structural profiles of bioactive polysaccharides from edible fruits representing different terrestrial biomes, relating them—with a focus on their monosaccharide fractions—to the abiotic variables of each biome, such as temperature, rainfall, annual water regimes, and physicochemical characteristics of the soil to provide an accurate landscape regarding the patterns and divergences surrounding the development of edible fruits around the world. The present review also provided a focus on the various analytical methods used to obtain data related to the glycosidic profile of the analyzed edible fruits, allowing for a comparison of issues relating to the biomes and the quantitative composition of the existing polysaccharides, together with the associated macromolecular parameters, such as degree of esterification, branching, and average molecular weight. From the analysis performed, recurrences of characteristics were identified in different biomes, such as high concentrations of galacturonic acid and arabinose in fruits from cold regions; abundance of xyloarabinan and galactan in fruits from arid areas; and greater branching, acetylation, and a lower degree of esterification in fruits subject to water variations that favor water retention and cell wall stability. These profiles suggest a strong association between the structure of polysaccharides and ecological adaptations that are crucial for their full development. The insights presented here are of the utmost importance in both basic and applied food science, indicating possible structural targets for selecting and engineering resistance in edible fruits under various abiotic stress conditions and guiding and providing direction for experimental studies that extend beyond classical methodologies. Full article

Soybean protein isolate (SPI) gel has been demonstrated to exhibit suboptimal stability and a coarse texture. Selective enzymatic hydrolysis modification has been demonstrated to effectively enhance the functional properties and structural stability of the protein. The objective of this study was to modify SPI using alkaline protease and papain. The impact of selective enzymatic hydrolysis on SPI was examined through the analysis of hydrolysis degree (DH), particle size, and protein purity. A systematic exploration was conducted in order to investigate the structural and quality characteristics of SPI gel. Indicators such as secondary structure changes, texture characteristics, water-holding capacity (WHC), rheology, and microstructure were analyzed. The findings indicate that when the DH of the SPI solution is 1%, its particle size is reduced relative to that when DH is 0.5%. The SDS-PAGE results indicated that alkaline protease could hydrolyze most of the 7S and 11S components in SPI into shorter peptides, while papain retained more of the 7S and 11S components and generated peptides with larger molecular weights. Fourier-transform infrared (FT-IR) spectral analysis indicated that following the process of enzymatic modification, the contents of α-helix and β-sheet in the secondary structure of SPI increased, while the contents of β-turns and random coils decreased. In the context of gel performance, it has been demonstrated that papain-modified SPI, attributable to its elevated content of macromolecular peptides, manifests superior WHC, hardness, springiness, cohesiveness, chewiness, storage modulus (G), and microstructure in comparison to alkaline protease-modified gel. Concurrently, the gel performance of papain modified SPI is significantly superior to that of unmodified SPI gel. This research provides a significant theoretical foundation and practical reference for promoting the efficient application of SPI in the domain of food processing. Full article

A comprehensive investigation was conducted focusing on two series of poly(lactic acid) (PLA)-based nanocomposites filled with small amounts (0.5 and 1.0%) of metal (Ag/Cu) nanoparticles (NPs). Our work aimed to synthesize PLA/Ag nanocomposites via in situ ring-opening polymerization (ROP), and for comparison purposes, the same materials were also prepared via solution casting followed by melt mixing. PLA/Cu nanocomposites were also prepared via melt extrusion. Gel permeation chromatography (GPC) and intrinsic viscosity measurements [η] showed that the incorporation of Ag nanoparticles (AgNPs) resulted in a decrease in the molecular weight of the PLA matrix, indicating a direct effect of the AgNPs on its macromolecular structure. Fourier-transform infrared spectroscopy (FTIR) revealed no significant changes in the characteristic peaks of the nanocomposites, except for an in situ sample containing 1.0 wt% of AgNPs, where slight interactions in the C=O region were detected. Differential scanning calorimetry (DSC) analysis confirmed the semi-crystalline nature of the materials. Glass transition temperature was strongly affected by the presence of NPs in the case of the in situ-based samples. Melt crystallized studies suggested potential indirect polymer–NP interactions, while isothermal melt crystallization experiments confirmed the nucleation ability of the NPs. The mechanical performance was assessed via tensile and flexural measurements, revealing that the in situ-based samples exhibited remarkable flexibility. Moreover, during the three-point bending tests, none of the in situ nanocomposite samples broke. In this context, next-generation PLA-based nanocomposites have been proposed for advanced applications, including flexible printed electronics. Full article

Soybean Soluble Polysaccharide (SSPS) is a natural anionic polysaccharide with protein content extracted from soybean residue. However, the impact of molecular weight and degree of esterification (DE) of soybean polysaccharides on protein stabilization remains a topic of debate. This study aimed to clarify the composition, macromolecular structure, and protein stabilization mechanism of SSPS and its various fractions with differing DEs and molecular weights (MWs). Nine polysaccharide fractions were isolated from three types of SSPSs with varying DEs and MWs using membrane ultrafiltration treatment. The analysis of monosaccharide composition and protein content reveals that the first component of soybean polysaccharides with high (847 kDa) molecular weight and low DE(SSPS20I) possesses the highest (7.25%) concentration of galacturonic acid (GalA) and a lower (0.83%) protein content compared to high-esterification SSPS. Meanwhile, the analysis of amino acids revealed that glutamic acid and aspartic acid were the primary amino acids across all protein components. It was also evident that alkaline treatment influenced the amino acid composition of SSPS. Atomic Force Microscopy (AFM) further substantiated that the components of SSPS exhibit distinct morphological and structural characteristics. The effects of SSPS fractions on the stability of Acidic Milk Drinks (AMDs) were investigated and evaluated using LUMi-Sizer. The results suggest that SSPS20I provided better stabilization in AMDs. This work establishes critical structure–property correlations, revealing that both DE and MW govern SSPS stabilization efficacy through synergistic effects of electrostatic repulsion, steric hindrance, and interfacial adsorption capacity. Full article

Collagen is widely used in tissue engineering due to its excellent biocompatibility; however, its limited intrinsic mechanical strength restricts its application in load-bearing environments. This study introduces dialdehyde starch (DAS) as a biocompatible macromolecular cross-linker to enhance the mechanical integrity of collagen hydrogels. Collagen gels were cross-linked with DAS during neutralization under optimized conditions, resulting in a significant increase in compressive stiffness (up to ~125 kPa), thereby improving their suitability for mechanically demanding applications. Degradation studies of DAS-crosslinked collagen confirmed the long-term stability of the gel, while post-neutralization heparin incorporation improved bifunctionality, as evidenced by increased surface retention. FT-IR analysis confirmed the successful DAS cross-linking and heparin conjugation while preserving the native collagen structure. Bioactivity assays of DAS-crosslinked and heparin-conjugated collagen gel demonstrated enhanced chondrocyte migration in PDGF-BB-functionalized gels and improved cell viability, proliferation, and matrix deposition in TGF-β3-treated constructs. Preliminary ex vivo culture using a rabbit osteochondral defect model showed promising tissue integration and glycosaminoglycan accumulation. These results highlight the potential of DAS-crosslinked and heparin-conjugated collagen hydrogels as mechanically robust and biologically supportive scaffolds for osteochondral tissue engineering and regenerative medicine applications. Full article

In the marine environment, plastic fragments are constantly engaged in a complex degradation process under exposure to various physical and chemical factors, one of which is ultraviolet (UV) radiation. These processes result in the formation of smaller micro- and nano-sized plastic particles, which are highly bioavailable to marine organisms. To clarify the toxicological effects of the exposure of degraded plastic on the marine organisms, the model used in this study was the Pacific mussel Mytilus trossulus and polymethylmethacrylate (PMMA), which is commonly found in marine debris. Using molecular and biochemical markers (DNA damage, lysosomal membrane stability, integral antiradical activity (IAA) of biological samples, and malondialdehyde (MDA) as a product of lipid peroxidation), the toxicity of pristine PMMA and photoaged (PMMA-UV) particles was assessed. Using Fourier transform infrared spectroscopy, the characteristics of the macromolecular changes in the chemical structure of PMMA-UV were obtained, with an oxidation index of 6.83 ± 0.46, compared to the pristine PMMA of 5.15 ± 0.54. Using a laser analyzer, the sizes of PMMA particles were determined, and it was found that after UV irradiation, the ratio of size groups changed—the proportion of particles with sizes of 500–1000 μm decreased, and the number of particles with sizes of 50–125 μm increased twofold. Analysis of mussel cell viability showed that after exposure to both types of PMMA microparticles, there was a decrease in the ability to retain neutral red dye in lysosomes: PMMA and PMMA-UV had a similar effect on hemocytes, reducing dye retention in cells to 55.2 ± 3.24% and 61.1 ± 1.99%, respectively. In gill and digestive gland cells, PMMA-UV particles reduced the stability of lysosomal membranes to a greater extent than PMMA. After PMMA and PMMA-UV particle exposure, the levels of DNA damage were as follows: in hemocytes, 10.1 ± 1.4% and 12.7 ± 0.8%, respectively; in gills, 7.8 ± 1.1% and 14.4 ± 2.9%, respectively; and in the digestive gland, 19.0 ± 1.3% and 21.9 ± 2.8%, respectively, according to the control values 3.6 ± 1.3%, 4.6 ± 1.1%, 5.1 ± 1.5%, respectively. According to the results of biochemical markers, the reaction of mussels to the presence of PMMA and PMMA-UV particles in the environment was tissue-specific: in the cells of the digestive gland, the level of IAA increased by 2 and 1.3 times compared to the control group of mussels (76.22 ± 6.77 nmol trolox/g wet weight and 52.43 ± 2.36 nmol trolox/g wet, respectively), while in the gill cells, the non-significant increase in antiradical activity was noted. An increase in MDA content was also observed in gill cells (255.8 ± 9.12 nmol MDA/g wet weight and 263.46 ± 9.45 nmol MDA/g wet weight, respectively) compared with the control group. This study showed that UV irradiation of PMMA microparticles increases their bioavailability and toxicity to M. trossulus. Full article