Search Results (1,496)

Thermoplastic starch (TPS) is a biodegradable polymer from renewable sources, but its limited mechanical and thermal properties restrict wider industrial use compared to petroleum-based plastics. In this study, TPS-based biocomposites were developed and optimized by incorporating agricultural and mineral Residues: coffee husks (CH), potassium feldspar (PF), and Bahia Beige marble (BB) as reinforcements. Mechanical, thermal, and morphological characterizations were carried out, and a simplex–lattice mixture design was applied to optimize the formulations. The 70/20/5/5 (TPS/CH/PF/BB, wt.%) composition achieved the highest tensile strength (2.0 MPa) and elastic modulus (70.2 MPa), while the 90/0/5/5 formulation showed superior impact resistance. FTIR and SEM analyses confirmed effective filler dispersion and strong matrix–filler interactions. Scheffé polynomial models (R² > 87%) accurately predicted performance, highlighting the reliability of the statistical approach. From a sustainability perspective, this work demonstrates that upcycling coffee husks and mineral residues into TPS-based biocomposites contributes to waste reduction, landfill diversion, and the development of cost-effective biodegradable materials. The proposed systems offer potential for eco-friendly packaging and agricultural applications, reducing dependence on fossil-based plastics and mitigating the environmental footprint of polymer industries. Statistical optimization further enhances efficiency by minimizing experimental waste. Moreover, this research supports circular economy strategies and provides scalable, sustainable solutions for waste valorization. Full article

Asphalt is a widely used polymeric material in pavement engineering. However, it is easily affected by heat and ultraviolet rays, which accelerate its molecular degradation and physicochemical aging, thereby limiting its service life. To improve the anti-aging properties of asphalt, three types of nano-zinc oxide (ZnO)-modified asphalt were prepared. The chemo-rheological behavior, structural evolution of polymeric components, molecular weight distribution, and nanoscale morphology of nano-ZnO-modified asphalt were studied via dynamic shear rheometry (DSR), Fourier transform infrared spectrometry (FTIR), gel permeation chromatography (GPC) and atomic force microscopy (AFM), and the aging resistance of nano-ZnO-modified asphalt was quantitatively analyzed using the rutting factor index, functional group index, molecular size ratio, and nanoscale parameters. The findings indicate that nano-ZnO enhances the high-temperature rheological properties of asphalt and delays the increase in the rutting factor of aged asphalt. Nano-ZnO is dispersed in the asphalt matrix in the form of a physical mixture without inducing new chemical bonds, and can reduce the nanoscale roughness of asphalt. After aging, the nanoscale roughness and the aspect ratio of the bee structure decreased, and the bee structure area increased. According to the changes in the functional group index and the proportions of molecular sizes in the asphalt, it was found that nano-ZnO can significantly improve asphalt’s aging resistance. The results of this study provide insights into the nanoscale modification and structure–property relationships of polymeric asphalt binders, providing a reference for the design and application of functional polymer nanocomposite systems with improved durability. Full article

Polybutylene succinate (PBS), as one of the most promising multi-application polymer, still suffers from low toughness, poor miscibility, and high crystallinity. Blending with starch is an effective strategy to improve the properties of PBS, but the compatibility and dispersity between starch and PBS still need to be optimized. In this study, mechanical ball milling was carried out to synthesize esterified starch and the subsequent PBS/esterified starch blend. The FT-IR and XPS analyses confirmed the existence of molecular interactions between PBS and esterified starch. SEM images showed a homogeneous surface for the PBS/esterified starch blend, highlighting the favorable compatibility and good dispersion of starch within the PBS matrix. TGA, DSC, and VSP tests indicated that the introduction of esterified starch into PBS lowered the thermal transition temperatures, thereby enhancing the processability. WCA measurements displayed that the water contact angle of the PBS/esterified starch blends gradually decreased with increasing esterified starch content, proving the improved hydrophilicity of PBS/esterified starch blends. Mechanical testing indicated that incorporating 5 wt% esterified starch into PBS significantly improved the tensile strength to 36.35 ± 2.16 MPa and the breaking elongation to 27.18 ± 5.08%, surpassing those of the pure PBS, PBS/esterified starch mixture, and PBS/starch blend. Our study indicates that mechanical ball milling is an efficient method to improve the properties of PBS composites. Full article

This study examines advanced cementitious composites incorporating Multi-Walled Carbon Nanotubes (MWCNTs), combining experimental investigations and analytical modeling for enhanced Structural Health Monitoring (SHM) applications. The experimental phase assessed the electrical properties of specimens with varying MWCNT contents, identifying a percolation zone between 0.05 wt% and 0.5 wt%. A dispersion protocol using ultrasonic agitation and a surfactant ensured the uniform distribution of CNTs. Furthermore, a novel micromechanical model, based on established polymer matrix approaches, was used to predict electrical conductivity behavior, accounting for nanotube geometry, concentration, waviness, and tunneling effects. Model predictions confirmed its effectiveness in analyzing structure–property relationships in CNT-based cementitious materials. Full article

In this study, the oxidative upgrading of heavy oil residues using polymer-containing waste for the sustainable production of bitumen was investigated. Oxidation was performed at temperatures of 250–270 °C for 3–4 h with the addition of 2–3 wt.% polyethylene-based waste, under an air flow of 7 L/min. The physical and mechanical characterization of the resulting bitumen demonstrated compliance with oxidized modified bitumen grades OMB 100/130 and OMB 70/100. FTIR spectroscopy revealed the formation of carbonyl and sulfoxide functional groups, indicating the effective oxidative transformation of the bitumen matrix and partial incorporation of polyethylene fragments. NMR spectroscopy confirmed increased aromaticity and carbonyl content, while also detecting polyethylene-derived signals, suggesting compatibility and integration of the polymer waste into the oxidized structure. The thermal and rheological results showed that the optimal conditions for producing high-quality oxidized bitumen involved the use of 2% polymer waste at 270 °C for 4 h, yielding enhanced physical properties and chemical stability. These findings support the feasibility of using polymer-containing waste for bitumen upgrading, offering both environmental and technical advantages. The method not only improves the quality of bitumen but also contributes to waste valorization and circular economy practices in the road construction industry. Full article

Hydroxypropyl methylcellulose (HPMC) is a biocompatible polymer widely used in topical formulations due to its suitable rheological behavior, film-forming capacity, and good compatibility with different active pharmaceutical ingredients. The present study demonstrates the potential of HPMC-based gels for dermal delivery of porphyrinic photosensitizers, aiming to enhance the efficiency of photodynamic therapy (PDT) in potential skin cancer applications. HPMC-based gel incorporating two previously synthesized porphyrinic photosensitizers, named 5,10,15,20-tetrakis-(4-acetoxy-3-methoxyphenyl) porphyrin (P2.1) and 5-(4-hydroxy-3-methoxyphenyl)-10,15,20-tris-(4-acetoxy-3-methoxyphenyl) porphyrin (P2.2), was developed and carefully characterized regarding its rheological behavior, texture, and in vitro activity. Fourier-transform infrared spectroscopy (FTIR), thermogravimetric analysis (TGA), X-ray diffraction (XRD), atomic force microscopy (AFM), fluorescence, and UV-Vis spectroscopy were carried out to evaluate the structural and morphological changes induced by the incorporation of the porphyrins in the HPMC gel matrix. The gels were subsequently evaluated by pharmacotechnical analysis, including pH (7.2 for both HPMC-P2.1 and HPMC-P2.2), viscosity, spreadability, texture profile analysis, and drug content uniformity. Rheological behavior confirmed the pseudoplastic behavior, suggesting a structured system with a gel-like consistency, while physical measurements demonstrated the stability and preserved functionality of the photosensitizers within the HPMC matrix. In vitro studies revealed an efficient cellular internalization of selected porphyrins into human epidermoid carcinoma cells, a critical requirement for topical PDT applications. The study highlights the capability of HPMC gels to serve as effective delivery platforms for porphyrin-based photosensitizers, supporting their application in localized skin cancer treatment through PDT. Full article

This study addresses the critical need for sustainable material development by thoroughly investigating the synergistic effects of artichoke stem waste (ASW) and titanium dioxide nanoparticles (TiO₂ NPs) on the properties of epoxy matrix composites. This research uniquely utilizes stereolithography (SLA)-based 3D printing technology for the fabrication and characterization of polymer matrix composites. The study systematically investigates three distinct composite formulations: artichoke stem waste/epoxy, TiO₂ nanoparticles/epoxy, and a novel hybrid of artichoke stem waste/TiO₂ nanoparticles/epoxy composites. Each formulation was prepared at three different loading concentrations to determine their optimal performance. The fabricated composites underwent comprehensive characterization, including meticulous evaluations of their mechanical (tensile), thermal (Thermogravimetric Analysis (TGA)), morphological (Scanning Electron Microscopy (SEM)), and chemical-bonding (Fourier Transform Infrared (FT-IR) spectroscopy) properties. Additionally, X-ray Diffraction (XRD) and FT-IR analyses were performed to structurally characterize the raw materials (pristine (cured epoxy), ASW, and TiO₂ NPs) and the final composite structures. The findings indicate that the incorporation of ASW and TiO₂ NPs significantly enhances the performance of epoxy composites. This discovery is significant as it demonstrates the successful valorization of agricultural waste into high-performance composite materials and advances the capabilities of 3D printing technology in sustainable materials science. The results of this study offer critical insights, substantially contributing to the development of sustainable and high-value materials. Full article

Architectural exterior wall coatings require a balance of elasticity, stain resistance, and durability. Although nano-SiO₂ enhances fracture resistance in elastic coatings, its limited hydrophobicity allows pollutant adhesion. Nano-TiO₂ can photocatalytically degrade organics but is often encapsulated by the polymer matrix, reducing its effectiveness. This study introduces a SiO₂-TiO₂ composite topcoat applied via aqueous dispersion to overcome these limitations. Experimental results demonstrate that the composite coating significantly outperforms single-component modifications, improving stain resistance by 21.3% after 12 months of outdoor exposure. The surface remains brighter with markedly reduced pollutant accumulation. Mechanistically, SiO₂ serves as an inert mesoporous carrier that improves the dispersion and photostability of TiO₂, minimizing agglomeration and photocorrosion. Its inherent hardness and hydrophobicity reduce physical adsorption sites. Together, SiO₂ and TiO₂ create a nanoscale rough surface that enhances hydrophobicity through a lotus-like effect. Under UV irradiation, TiO₂ generates radicals that decompose organic pollutants and inhibit microbial growth, enabling efficient self-cleaning with rainwater. This synergistic mechanism addresses the limitations of individual nanoparticles, successfully integrating elasticity with long-term anti-fouling and durability. This composite demonstrates a significant advancement in stain resistance and overall durability, offering potential applications in energy-efficient and environmentally sustainable building technologies. Full article

Background: The treatment of wounds remains a significant clinical challenge, particularly in chronic and infected wounds, where delayed healing often results in complications. Recent advances in biomaterials have highlighted the potential of polymer-based scaffolds as promising platforms for wound management due to their ability to mimic the extracellular matrix, support tissue regeneration, and provide a moist environment conducive to healing. Objectives: This review aims to provide a comprehensive overview of the recent progress in the design and application of polymer-based scaffolds loaded with essential oil (EO) components, emphasizing their role in promoting effective wound healing. Methods: Relevant literature on polymeric scaffolds and EO-based bioactive agents was systematically reviewed, focusing on studies that investigated the biological activities, fabrication techniques, and therapeutic performance of EO-loaded scaffolds in wound management. Results: Findings from recent studies indicate that EO components, particularly monoterpenoids such as thymol, carvacrol, and eugenol, exhibit remarkable antimicrobial, anti-inflammatory, antioxidant, and analgesic properties that accelerate wound healing. When incorporated into polymer matrices, these components enhance scaffold biocompatibility, antimicrobial efficacy, and tissue regeneration capacity through synergistic interactions. Conclusions: The integration of essential oil components into polymeric scaffolds represents a promising strategy for developing multifunctional wound dressings. Such systems combine the structural advantages of polymers with the therapeutic benefits of EOs, offering an effective platform for accelerating healing and preventing wound infections. Full article

Background/Objectives: Citrus × paradisi Macfad., Rutaceae. peel is a rich source of naringin (NR), but its poor solubility and low bioavailability limit applications. This study aimed to improve NR delivery by comparing microencapsulation, liposomal microencapsulation, and buccal films containing either pure NR or grapefruit peel extract. Methods: Four spray-dried powder formulations—spray-dried NR (NS), liposomal NR (NLS), spray-dried extract (ES), and liposomal extract (ELS)—were produced using maltodextrin, β-cyclodextrin, and HPMC as wall materials. Buccal films (EP1, EP2, NP1, NP2) were prepared via solvent casting with HPMC, alginate (ALG), or polyvinyl alcohol (PVA). All samples were evaluated for solubility, moisture content, mucoadhesion, and in vitro release under simulated gastric, intestinal, and salivary conditions. Results: NR powders had the highest absolute solubility (306.42 ± 10.34 µg/mL), whereas ELS showed the lowest due to low loading. However, relative to theoretical NR content, ELS achieved the highest dissolution efficiency (55.3%), followed by NLS (42.7%), outperforming NS (5.6%) and ES (91.8%) in sustained release potential. Dual encapsulation (NLS, ELS) slowed gastric release and maintained intestinal delivery, while non-liposomal powders released rapidly. In buccal films, NP2 (NR + PVA) showed the highest release (69.97 ± 3.01 µg/mL; 40.9% efficiency) and strongest mucoadhesion (0.47 N·s). Extract-based films had lower absolute NR release but higher relative efficiency to content, likely due to co-extracted compounds enhancing wettability and matrix erosion. Conclusions: Liposomal microencapsulation improves relative dissolution efficiency and sustains intestinal release, while PVA-based buccal films enhance both release and mucoadhesion. Polymer choice and active ingredient composition are critical for optimising oral delivery of NR. These results demonstrate the potential of the proposed systems in the pharmaceutical or dietary supplement field, especially in improving the oral delivery of poorly soluble flavonoids. A graphical summary is included, visually summarising the main formulation strategies and results. Full article

This work presents a comprehensive study on the synthesis and application of Al₂O₃ fibers derived from an ammonium aluminum carbonate hydroxide (AACH) precursor. Through a hydrothermal route, the influence of critical synthesis parameters, including aluminum nitrate and urea concentrations, reaction temperature and time, and stirring conditions, on fiber morphology and aspect ratio was systematically investigated. The as-synthesized AACH fibers were subsequently converted into thermodynamically stable α-alumina fibers via controlled annealing. These high-aspect ratio alumina fibers were incorporated into polydimethylsiloxane (PDMS) to produce electrically insulating, thermally conductive composites. The thermal performance of fiber-filled composites was benchmarked against that of particle-filled counterparts, with the former exhibiting significantly enhanced thermal conductivity. Furthermore, the dielectrophoretic alignment of alumina fibers led to an additional increase in thermal conductivity, underlining the importance of high-aspect ratio fillers. This study uniquely combines the controlled synthesis of alumina fibers with their incorporation and alignment in a polymer matrix, presenting a novel and effective approach for engineering anisotropic, thermally conductive, and electrically insulating composite materials. Dielectrophoretic alignment of α-Al₂O₃ fibers synthesized through optimized hydrothermal conditions and incorporated into PDMS composites deliver over 95 % higher thermal conductivity than spherical fillers. Full article

The delamination of building facades creates a critical demand for inorganic adhesive mortars with high long-term adhesion. Geopolymer (GP) represents an eco-friendly alternative to Portland cement (PC). However, the effect of polymer additives, commonly used in cement-based adhesive mortars, on GP mortar remains insufficiently studied. This study examines the effects of hydroxypropyl methylcellulose (HPMC) and vinyl acetate-ethylene (VAE) polymer on the workability, mechanical properties, durability, and microstructure of GP mortar. Results show that an optimal HPMC content (0.4 wt%) improves the fluidity, compressive strength, and adhesive strength of GP mortar, approximately 6%, 16%, and 20%, respectively. These enhancements are attributed to the incorporation of uniformly distributed microbubbles in the mortar matrix. Beyond this optimal content, however, HPMC impairs flowability and adhesion due to its thickening effect. In contrast, VAE addition significantly enhanced adhesive strength by approximately 28%, albeit at the cost of a 17% reduction in compressive strength, resulting from the retardation of the alkali activation process. This gain in adhesion is associated with the formation of a continuous polymer film that establishes both physical interlocking and chemical bonding with the GP matrix. Furthermore, HPMC improved the durability of the GP mortar, while VAE did not contribute to this aspect. These insights offer valuable guidance for designing high-performance GP-based adhesive mortars suitable for building applications. Full article

Highly permeable and selective membranes are crucial for energy-efficient gas separation. Two-dimensional (2D) graphitic carbon nitride (g-C₃N₄) has attracted significant attention due to its unique structural characteristics, including ultra-thin thickness, inherent surface porosity, and abundant amine groups. However, the interfacial defects caused by poor compatibility between g-C₃N₄ and polymers deteriorate the separation performance of membrane materials. In this study, amino-functionalized g-C₃N₄ nanosheets (CN@PEI) was prepared by a post-synthesis method, then blended with the polymer Pebax to fabricate Pebax/CN@PEI mixed matrix membranes (MMMs). Compared to g-C₃N₄, MMMs with CN@PEI loading of 20 wt% as nanofiller exhibited a CO₂ permeance of 241 Barrer as well as the CO₂/CH₄ and CO₂/N₂ selectivity of 39.7 and 61.2, respectively, at the feed gas pressure of 2 bar, which approaches the 2008 Robeson upper bound and exceeded the 1991 Robeson upper bound. The Pebax/CN@PEI (20) membrane showed robust stability performance over 70 h continuous gas permeability testing, and no significant decline was observed. SEM characterization revealed a uniform dispersion of CN@PEI throughout the Pebax matrix, demonstrating excellent interfacial compatibility between the components. The increased free volume fraction, enhanced solubility, and higher diffusion coefficient demonstrated that the incorporation of CN@PEI nanosheets introduced more CO₂-philic amino groups and disrupted the chain packing of the Pebax matrix, thereby creating additional diffusion channels and facilitating CO₂ transport. Full article

Y₂O₃ nanoparticles were used in a polyethersulfone (PES) as additives to increase the permeation properties of the polymeric membranes. Membranes were manufactured by diffusion-induced phase inversion in N-methyl-pyrrolidone (NMP) using a different concentration of nanoparticles. Y₂O₃ is used in polymeric membranes to enhance their functional properties, especially in wastewater treatment processes. Incorporating Y₂O₃ nanoparticles into the polymer matrix improves the membrane’s hydrophilicity, permeability, and mechanical strength. Additionally, Y₂O₃ provides better properties and reduces fouling. Recent studies highlight its potential as a modifying agent for advanced composite membranes. This paper investigated challenges in the synthesis of Y₂O₃-enhanced membranes and links synthesis with performance. It was observed that the composite membranes have better permeation properties by adding a small amount of Y₂O₃. For membranes at 21 wt.% PES permeability increase from 107 to 112 L/m²·h/bar. Fouling performance increases by adding nanoparticles, relative flux decreases by 30% for membranes without nanoparticles and by 10% for membranes with nanoparticles, both at a concentration of 25% PES. Rejection increases for membranes at 21%Pes from 21% for membranes without nanoparticles to 39% for membranes with nanoparticles. The influence of Y₂O₃ nanoparticles on the membranes’ performance was determined by filtration experiments to establish the permeability, fouling, retention, and the water flux; by contact angle to establish the surface hydrophilicity; and by SEM to investigate the membranes’ structures. Full article

Molecularly imprinted polymer (MIP) biosensors offer an attractive strategy for selective biomolecule detection, yet imprinting proteins with structural fidelity remains a major challenge. In this work, we present a rationally designed electrochemical biosensor for matrix metal-loproteinase-8 (MMP-8), a key salivary biomarker of periodontal disease. By integrating graphene oxide (GO) with electropolymerized poly(eriochrome black T, EBT) films on screen-printed carbon electrodes, the partially reduced GO interface enhanced electrical conductivity and facilitated the formation of well-defined poly(EBT) films with re-designed polymerization route, while template extraction generated artificial antibody-like sites capable of specific protein binding. The MIP-based electrodes were comprehensively validated through morphological, spectroscopic, and electrochemical analyses, demonstrating stable and selective recognition of MMP-8 against structurally similar interferents. Complementary density functional theory (DFT) modeling revealed energetically favorable interactions between the EBT monomer and catalytic residues of MMP-8, providing molecular-level insights into imprinting specificity. These experimental and computational findings highlight the importance of rational monomer selection and nanomaterial-assisted polymerization in achieving selective protein imprinting. This work presents a systematic approach that integrates electrochemical engineering, nanomaterial interfaces, and computational validation to address long-standing challenges in protein-based MIP biosensors. By bridging molecular design with practical sensing performance, this study advances the translational potential of MIP-based electrochemical biosensors for point-of-care applications. Full article