Search Results (6,438)

Standard laboratory protocols for simulating short-term asphalt aging, including the Thin-Film Oven Test (TFOT) and Rolling Thin-Film Oven Test (RTFOT), are widely adopted but frequently lack sensitivity to the distinct thermo-oxidative kinetics of high-viscosity and polymer-modified systems. This study evaluates a severity-graded aging matrix incorporating the Pressure Aging Vessel (PAV) at variable durations (2, 5, and 10 h at 163 °C/2.1 MPa) as a potential alternative to conventional thin-film methods. Three binder systems BA-70 (PG 64-22), SBS-modified, and compatibilized functional thermoplastic (CFT)-modified asphalt were subjected to TFOT, RTFOT, and PAV variants. Comprehensive rheological characterization (DSR frequency/temperature sweeps, rutting parameter, MSCR) and SARA fractionation were employed to quantify oxidative stiffening, permanent deformation resistance, and compositional evolution. An Aging Severity Index (ASI) was developed to normalize multi-parameter responses and establish quantitative protocol equivalence thresholds. BA and SBS-modified binders exhibited pronounced protocol-dependent stiffening, with PAV-5h vs. RTFOT ASI gaps of 30.0% and 33.0%, respectively, confirming distinct aging severity under the tested conditions. Conversely, the CFT-modified binder demonstrated a compressed aging signature, maintaining stable complex modulus, minimal non-recoverable compliance escalation, and near-complete elastic recovery across all protocols. The ASI gap between PAV-5h and RTFOT for CFT was 6.0%, falling within the pre-defined ≤7% equivalence threshold established from combined rheological test uncertainty, specification-aligned engineering tolerance, and empirical gap clustering. SARA analysis corroborated these findings, showing CFT retained higher aromatic/resin fractions while limiting asphaltene accumulation compared to BA-70 and SBS. Importantly, the observed interchangeability between PAV-5h and RTFOT is strictly limited to the specific CFT-modified binder formulation tested under laboratory conditions. Broader specification adoption requires targeted validation across diverse modifier chemistries, dosages, and field-aged binders before generalization. Full article

Micro- and nanoplastic (MNP) pollution has emerged as a global environmental and health concern, driving the rapid development of sensor technologies for faster, more sensitive, and field-deployable detection. This review synthesizes recent advances in optical, electrochemical, and biosensor platforms for MNP analysis and compares their analytical performance and practical feasibility. Optical sensors, including plasmonic, spectroscopic, and colorimetric systems, enable label-free and often rapid detection with material discrimination capability, and are well-suited for screening applications, though they commonly exhibit higher detection limits and matrix interference. Electrochemical sensors demonstrate the highest analytical sensitivity overall, frequently reaching low µg L⁻¹ to ng mL⁻¹ levels, with strong potential for miniaturization and on-site deployment; performance is further enhanced by nanostructured electrodes, photoelectrochemical designs, and signal amplification strategies. Biosensors incorporating peptides, aptamers, enzymes, or engineered proteins provide improved polymer selectivity and enable targeted detection, but face challenges related to stability, cross-reactivity, and reproducibility in complex samples. Practically, portable electrochemical and simple optical colorimetric platforms are currently the most feasible for field use, while hybrid bio-electrochemical systems show the highest performance potential. Future research should prioritize robust selective recognition elements, antifouling interfaces, standardized validation protocols, mixed-polymer quantification models, and integration with machine learning to enable reliable, real-world MNP monitoring. Full article

This experimental study systematically explores the impact of particle size variation in Layered Double Hydroxide (LDH) composites on the thermomechanical and optical properties of poly(methyl methacrylate) (PMMA) nanocomposites. Utilizing a co-precipitation method, LDHs modified with cocamidopropyl betaine (CPB) were synthesized in three distinct sizes (small 80 nm, medium 130 nm, and large 280 nm) and then incorporated into a PMMA matrix through bulk polymerization using Benzoyl Peroxide as the initiator. Morphological analysis via electron microscopy confirmed the exfoliation of LDHs layers within the PMMA matrix, indicating effective dispersion. The medium-sized LDH/PMMA nanocomposite exhibited enhanced interlayer interactions, facilitating polymerization and increasing the thermal degradation onset temperature by 21.2 °C compared to pristine PMMA. In contrast, the small-sized LDH/PMMA nanocomposite demonstrated a significant improvement in mechanical performance, with a 62% increase in storage modulus, attributed to its higher aspect ratio and improved stress transfer. Additionally, the optical transmittance of the nanocomposites across a visible range of 550 nm exceeded 88%, suggesting a minimal impact on optical clarity despite varied particle sizes. Overall, the incorporation of size-specific LDHs modifications led to notable enhancements in both the thermal stability and mechanical performance of the PMMA nanocomposites, underlining the potential of tailored nanoparticle modifications in advanced polymer matrices. Full article

Soil micro- and nanoplastic contamination is escalating globally, yet its potential to interfere with routine agrochemical analyses remains poorly quantified. Standard operating procedures (SOPs) were calibrated for natural soil matrices and may not account for synthetic, carbon-rich polymers. This controlled model study quantified the analytical sensitivity of FAO/GLOSOLAN/ISO standard procedures to polystyrene nanoparticle (50 nm) contamination across a 0–0.5% (w/w) gradient in a Luvic Chernozem. Key parameters—pH, soil carbon, total nitrogen (TN), cation exchange capacity (CEC), and clay fraction—were measured following standardized protocols. The Walkley–Black method exhibited a strong dose-dependent increase in measured SOC (r = 0.93), reflecting systematic overestimation due to dichromate co-oxidation of polymer matrix, likely facilitated by exothermic heating above polystyrene’s glass transition temperature. The Dumas method showed moderate correlation (r = 0.59) but higher replicate variability driven by small aliquot size and heterogeneous nanoparticle distribution. The pH measurements displayed non-linear responses and elevated variability at low doses, whereas TN, CEC, and clay content remained statistically stable. These findings demonstrate that nanoplastic contamination can introduce significant analytical artifacts in oxidation-based SOC determinations, potentially leading to misinterpretation of soil carbon trends. Given the single-soil, single-polymer design, results represent a system-specific proof of analytical vulnerability rather than a universally quantified bias. Laboratories analyzing potentially contaminated soils should exercise caution with wet-oxidation SOC data, and broader SOP revisions must await multi-soil, multi-polymer validation campaigns. Full article

Nanocomposites consisting of titanium carbonitride nanoparticles (TiCN) and epoxy resin were fabricated and studied as the filler content was varied. Nanocomposites’ structural investigation was conducted via X-ray Diffraction technique (XRD), while their morphology was examined by employing Scanning Electron Microscopy (SEM). Viscoelastic mechanical properties were assessed by Dynamic Mechanical Thermal Analysis (DMTA). Results revealed the reinforcing ability of TiCN nanoparticles. The dielectric characterization of the nanocomposites was carried out using Broadband Dielectric Spectroscopy (BDS) over a wide frequency and temperature range. Dielectric spectroscopy revealed two relaxation processes related to the polymer matrix: the α-relaxation, associated with the glass-to-rubber transition, and the β-relaxation, associated with the rearrangement of side polar groups. In addition, in the low-frequency–high-temperature region, interfacial polarization (IP) was observed. IP is related to the presence of nanoparticles and to the accumulation of unbound charges at the system’s interface and includes contributions from a dipolar process and charge migration (conductivity). Alternating current conductivity generally increases with filler content, though it is also affected by frequency and temperature. Conductivity could influence Electrode Polarization (EP), which often masks the dipolar process of IP. A simple method for removing the EP effect is formulated and tested. Full article

The food-packaging sector is undergoing a major transition driven by the environmental burden associated with petroleum-based plastics and the increasing demand for sustainable alternatives. In this context, biodegradable packaging materials capable of extending food shelf life through active preservation functions have attracted considerable interest. Cellulose is the most abundant natural polymer and an attractive candidate for sustainable packaging; however, it lacks intrinsic antimicrobial activity. In the present study, innovative carboxymethyl cellulose (CMC)-based composite films were developed by incorporating zinc oxide (ZnO) nanoparticles (NPs) and thyme essential oil (TEO) as antibacterial active agents. The obtained films exhibited strong antibacterial activity against both Escherichia coli and Staphylococcus aureus, completely eliminating planktonic cell viability after 3 h of contact and producing inhibition zones of up to 30 mm. In addition to their biological performance, the composite films showed improved mechanical and functional properties. ZnO NPs appear to act as multifunctional junctions within the CMC matrix, while the dispersed TEO droplets contribute, together with the inorganic phase, to reduced water-vapor transfer. The films retained good transparency in the visible range while exhibiting UV-A transmittance below 7%, indicating enhanced light-barrier performance. Preliminary tests on soft cheese indicated shelf-life extension up to 14 days at 4 °C, while in inoculated cheese slices packed in the composite films, S. aureus was not detected from the 3rd day. Overall, these results demonstrate the potential of CMC/ZnO/TEO composite films as biodegradable active packaging materials for perishable food products. Full article

Hydrogel scaffolds have emerged as a central platform in tissue engineering due to their ability to mimic the extracellular matrix and support cellular functions. Among natural polymers, chitin and its derivative chitosan have emerged as valuable candidates for hydrogel scaffold development because of their biodegradability, compatibility with living tissues, and inherent biological functionality; however, their distinct and complementary roles in hydrogel scaffold design are often insufficiently differentiated in the literature. This review provides a comprehensive and mechanism-driven analysis of chitin- and chitosan-based hydrogel scaffolds, emphasising how their molecular structure governs network formation, mechanical performance, and biological functionality. Chitin is highlighted primarily as a structurally robust and crystalline component suitable for reinforcement. In contrast, chitosan serves as a versatile, soluble, and chemically reactive matrix enabling various crosslinking and functionalization strategies. Recent advances in physical, ionic, and covalent crosslinking as well as composite scaffold engineering, biofunctionalization, and emerging fabrication approaches such as injectable systems and three-dimensional bioprinting are systematically examined. The relationships between scaffold architecture, degradation behaviour, and cellular responses are discussed in key tissue engineering applications, including bone, cartilage, skin, and nerve regeneration. Importantly, this review introduces a unified structure–property–function framework that distinguishes the roles of chitin and chitosan within hydrogel systems and links crosslinking mechanisms to application-specific performance requirements, an aspect not comprehensively addressed in previous studies. Current challenges related to mechanical limitations, material variability, and clinical translation are critically evaluated, and future perspectives for the rational design of next-generation biomimetic hydrogel scaffolds are proposed. Full article

In materials science, the increasing use of lightweight and multi-material structures has made improving the interfacial bonding characteristics of polymer-based adhesive systems increasingly important. Accordingly, chemical surface activation and interfacial engineering strategies have attracted considerable attention for enhancing polymer–fiber compatibility and adhesion performance. However, the combined effects of fiber content, surface treatment, and orientation on adhesion behavior remain insufficiently understood. In the present study, natural fibers obtained from the rachis part of the palm tree were chemically modified and incorporated into an epoxy adhesive matrix to investigate the effect of surface functionalization on polymer–fiber interfacial adhesion. In the first stage, the effects of fiber ratios (5–20 wt%) and chemical surface treatments (methanol cleaning and methanol +2–6% HNO₃) on adhesion behavior were evaluated. Tensile tests showed that specimens treated with methanol cleaning followed by 4% HNO₃ oxidation and containing 10 wt% fiber exhibited an approximately 48% increase in failure load compared to neat joints. In the second stage, the influence of fiber orientation (0–90°) was examined using the optimized parameters. The results indicate that interfacial load-transfer capability increased as the fiber orientation approached perpendicular alignment, reaching maximum performance at 90°. Based on SEM observations, nitric acid treatment was found to increase the surface roughness of the fibers and strengthen the polymer–fiber interfacial bond. FTIR, XPS and contact angle measurements suggested the development of oxygen-containing surface functionalities and improved wettability, consistent with enhanced interfacial adhesion. These findings demonstrate that appropriate chemical surface treatment, fiber content, and orientation can effectively enhance the interfacial adhesion and bonding efficiency of epoxy-based adhesive systems, providing practical guidance for the design of high-performance bonded structures. Full article

Textile-reinforced concrete (TRC) beams have attracted widespread interest in recent years as an alternative to fiber-reinforced polymer (FRP) techniques. However, despite their effectiveness, they are often associated with high material cost, sensitivity to elevated temperatures, and limitations in bonding performance under certain environmental and surface conditions. This research examines incorporating textile reinforcement internally (INT) by supplementing steel bars with glass fiber grids, as well as externally (EXT) by retrofitting existing members. The experimental work evaluates five RC beams: a control (CTR), two INT beams strengthened with alkali-resistant glass fabric textile (AR-GFT), one using one layer (INT1L) and the other three layers (INT3L), and two EXT beams where AR-GFT is bonded with mortar, again with one layer (EXT1L) and three layers (EXT3L). Altogether, 10 beams were tested, with duplicate specimens for every configuration. Observing load-deflection responses, cracking behavior, and the strengthening system’s performance revealed that AR-GFT contributes to enhanced load-bearing resistance in the RC beams. The INT1L beams exhibited negligible improvement compared with the CTR specimen, suggesting that internal strengthening alone does not meaningfully increase strength. Conversely, the INT3L beams demonstrated a 45% rise in strength for one sample, although the second performed similarly to the CTR specimen owing to slippage between the textile and adjacent matrix. EXT3L beams achieved up to a 90% increase in load-bearing capacity in one specimen. Nevertheless, the second specimen exhibited textile layer debonding and performed similarly to the CTR beam, underlining the necessity for correct textile positioning and sufficient mortar impregnation during application. Moreover, a three-dimensional (3D) nonlinear finite-element analysis (FEA) was performed to replicate beam responses, showing strong correlation with experimental observations. Overall, the results indicate that textile-based strengthening systems can successfully retrofit and upgrade RC structures, provided meticulous attention is paid to the quality and execution of the installation process. The study provides new insights into the flexural behavior of textile-strengthened RC beams, particularly in terms of the interaction between internal and external textile reinforcement with conventional steel. Full article

Three-dimensional braided carbon-fiber-reinforced polymer (CFRP) composites are promising for lightweight aircraft propeller blades. Aircraft composite structures may approach temperatures of 80–90 °C under the combined effects of solar radiation, infrared heating, and ground reflection. Yet the thermo-mechanical failure mechanisms of low-braiding-angle architecture remain insufficiently understood. This study comparatively investigates the tensile behavior and damage evolution of low-angle four-directional (3D4A-20°) and five-directional (3D5A-20°) braided CFRP composites under axial tension at both room temperature and 90 °C. A multi-scale approach integrating in situ X-ray computed tomography, digital image correlation, digital volume correlation, and scanning electron microscopy was used to characterize strain localization, internal cracking, and fracture morphology. At room temperature, 3D5A-20° shows higher stiffness and strength than 3D4A-20° because additional axial yarns improve load-transfer and three-dimensional constraint. At 90 °C, matrix softening and interfacial degradation accelerate crack initiation, strain localization, and damage propagation in both architectures. Nevertheless, 3D5A-20° maintains more stable and progressive damage evolution, whereas 3D4A-20° exhibits earlier crack coalescence and greater mechanical degradation. Overall, elevated temperature accelerates damage evolution through matrix softening and interfacial degradation, whereas braided architecture determines load transfer and crack connectivity. These findings provide guidance for the design of low-angle braided composites for thermally exposed aircraft propeller blades. Full article

The complete removal of persistent aromatic organic pollutants from aqueous environments demands the development of sustainable and highly efficient filtration materials. In this study, novel bio-sourced mixed-matrix membranes (MMMs) were successfully fabricated by incorporating the highly porous metal–organic framework MIL-68(Al) into a biodegradable polylactic acid (PLA) matrix via a solvent-induced phase inversion method. The integration of MIL-68(Al) nanoparticles significantly tailored the membrane’s morphological structure, endowing the hybrid membranes with enhanced surface hydrophilicity (water contact angle reduced from 90.3° to 72.7°) and superior permeability. The pure water flux reached an optimal value of 42.2 L m⁻² h⁻¹ at a 15 wt.% MOF loading. Crucially, the hybrid membranes exhibited exceptionally high adsorptive removal performance for p-nitrophenol (PNP) and methylene blue (MB). Driven by the abundant accessible active sites of the MOF filler, the MIL-20/PLA membrane achieved a maximum equilibrium adsorption capacity of 121.03 μg/cm² (36.90 mg/g) for PNP, representing a remarkable 25.7-fold enhancement over the pristine PLA membrane. Kinetic analyses confirmed that the adsorption process is strictly governed by pseudo-second-order kinetics, indicating a chemisorption mechanism dominated by hydrogen bonding and π–π stacking interactions. Furthermore, the optimized membranes demonstrated outstanding dynamic filtration efficiencies (>80%) and robust regenerability over multiple continuous operating cycles. This work not only highlights the synergistic interfacial effects between MOFs and biodegradable polymers but also provides a highly effective, eco-friendly, and sustainable membrane platform for the advanced remediation of organic-contaminated wastewater. Full article

Oil and gas well cement is routinely exposed to aggressive chemical and mechanical environments that can compromise long-term zonal isolation. Conventional Portland cement systems, which rely on hydration products such as calcium silicate hydrate (C–S–H), are particularly vulnerable to acid attack, carbonation, high salinity, and thermal stress. This study investigates a polymer–mineral composite cement in which Class F fly ash is incorporated into an epoxy resin matrix at 0, 25, and 50 weight percent (wt%) loading. The composite samples were exposed for ten days to harsh downhole-representative environments, including hydrochloric acid (HCl, 15–28 wt%), sodium hydroxide (NaOH, 15–28 wt%), sodium chloride (NaCl) brines (20 wt%), crude oil, elevated temperatures up to 100 °C, and high-pressure carbon dioxide (CO₂). Compressive strength was evaluated using a universal testing machine, capturing both deformation strength and ultimate failure strength to assess elastic and structural performance. Across most conditions, the composite maintained strengths exceeding 5000 psi, demonstrating strong chemical resistance. Acidic and CO₂ exposures primarily reduced elastic deformation rather than ultimate strength, suggesting localized interaction with the polymer matrix. Elevated temperature reduced strength to ~2800 psi and diminished elasticity, marking the material’s upper thermal limit. Acetone exposure progressively degraded the polymer network, highlighting potential controlled removability. These findings indicate that embedding industrial fly ash in a polymer matrix produces a mechanically resilient and chemically robust cement alternative with up to 50 wt% industrial waste incorporation. This hybrid system offers a promising approach for wells exposed to acidic, CO₂-rich, or high-salinity environments, where conventional Portland cement may fail. Full article

The utilization of waste, defined as commercially worthless or discarded material, is becoming an increasingly important topic in the context of environmental material overload. Thus, the development of new products should integrate waste, adding commercial value to materials that would have otherwise been discarded. In this context, Material Extrusion (ME), the most widely used technique in Additive Manufacturing (AM), has introduced a new manufacturing model, opening opportunities for developing innovative products. On the other hand, during the beneficiation process of ornamental rocks, tons of mineral waste are generated. This study aims to develop a polylactic acid (PLA) filament using Beige Bahia marble waste as a raw material source via the ME technique. Compositional mapping through Energy Dispersive Spectroscopy (EDS) indicated that, as the mass fraction increased, particle clustering within the PLA matrix decreased. Mass compositions ranging from 0–30% mineral waste to PLA were evaluated. Gel Permeation Chromatography (GPC) showed that the PLA molar mass in the PLA00 and PLA30 compositions was 109,103 and 120,103 g.mol⁻¹, respectively, indicating that the mineral waste helped preserve the polymer’s molar mass during material processing. An increase was observed in the elastic modulus. The total roughness profile demonstrated higher values for pure PLA, while the partial roughness profile showed higher noise due to the greater presence of particles on the surface. The final product exhibited characteristics like the original rock and could serve as an alternative when such features are desired. Full article

The application of lignin-based films is often restricted by traditional processing methods that rely on toxic organic solvents and harsh chemical reagents, which result in poor compatibility with the polymer matrix and difficulty balancing transparency, barrier, and toughness. Here, lignin was green-modified by ternary deep eutectic solvent (choline chloride-lactic acid-ethanol), and ZnO hybrids with cellulose nanocrystals (CNC) as anchor points were introduced to realize the stability and uniform dispersion of ZnO in the polyvinyl alcohol (PVA) matrix. The prepared composite film maintains a transmittance of about 78% at 800 nm while achieving a wide spectrum of ultraviolet shielding. The barrier properties of the film were markedly improved: the water vapor permeability (WVP) decreased to 0.24 × 10⁻⁷ g·m⁻¹·h⁻¹·Pa⁻¹, and the oxygen permeability (OTR) to 6.98 cm³·m⁻²·24 h⁻¹·0.1 MPa⁻¹. In addition, the mechanical flexibility and durability of the material were significantly improved, as evidenced by a tensile strain of 109%. In the insurance experiment, compared with the blank film, the browning degree and weight loss of the composite film were relatively low. The scalable and low-solvent consumption route provides a practical idea for the application of lignin in food preservation. Full article

The temperature sensitivity coefficient greatly affects the interior ballistic performance of propellant charges. Even under consistent loading conditions, variations in environmental temperature can lead to maximum chamber pressure fluctuations of 40–80 MPa, thereby compromising weapon efficiency and operational safety. In order to obtain a single-base propellant with a higher energy and lower temperature sensitivity coefficient, ultra-fine RDX particles were added into the single-base propellant. The difference in thermal expansion coefficients between RDX and the single-base propellant matrix leads to temperature-dependent microcracking. These microcracks increase the burning surface area at low temperatures, compensating for the reduced chemical reaction rate and thereby lowering the temperature sensitivity coefficient. A scanning electron microscope (SEM) was used to observe the inner structure of the single-base propellant with and without RDX particles. The thermal mechanical analysis (TMA) results, together with SEM observations, reveal that the interfaces between the propellant matrix and the RDX particles are temperature-dependent. As a result, the burning surface area of the modified single-base propellant varies with temperature, contributing to a reduced temperature sensitivity coefficient. Closed bomb tests were conducted to verify this inference, and the obtained curves and relevant quickness (RQ) values showed that the modified single-base propellant had stable burning behavior and lower temperature sensitivity. This study leverages the structural interactions between high-energy fillers and polymer matrices to provide a potential strategy for designing climate-resilient ammunition. Full article