Search Results (525)

In this study, polylactic acid (PLA) was blended with poly(ε-caprolactone) (PCL) and reinforced with nanosilica (SiO₂) to tailor surface characteristics and improve adhesion in biopolymer-based printed packaging applications. The surface microstructure and topography were analyzed using FTIR-ATR, SEM, and surface profilometry. Surface wettability and surface free energy (SFE), along with the adhesion properties of printed ink layers on polymer blends, were assessed, and the optical properties of the substrates and prints were evaluated. SEM revealed that PLA/PCL blends exhibited phase-separated morphologies with PCL droplet domains, whereas incorporation of 3 wt% SiO₂ resulted in finer dispersion and reduced surface irregularities. Surface roughness (Ra) increased from 1.92 µm for PLA/SiO₂ 100/3 to 4.45 µm for PLA/PCL/SiO2 50/50/0, while water contact angle decreased from 70.9° for neat PLA to 43.4° for PLA/SiO₂ 100/3 surface, reflecting enhanced hydrophilicity. SFE components ranged from 26 to 40.7 mJ/m² (dispersive) and 3.2 to 21.5 mJ/m² (polar). Adhesion parameters (interfacial tension ranging from 0.01 to 5.54 mJ/m², work of adhesion from 76.9 to 97.3 mJ/m², and wetting coefficient from 3.04 to 11.1 mJ/m²) indicated favorable ink compatibility for most blends, and optical density of the printed layers (1.85–2.35) confirmed potential for good printability. These findings demonstrate that PLA/PCL/SiO₂ blends allow controlled tuning of surface morphology, wettability, and adhesion, providing a promising approach for biodegradable and print-ready packaging substrates. Full article

Stretchable semiconductors capable of maintaining electrical performance under large mechanical deformation are essential for reliable wearable electronic devices. However, polymer semiconductors often suffer from electrical degradation when subjected to tensile strain. In this study, electrical stability under strain was achieved by using a rubber-blended poly(2,5-bis(2-octyldodecyl)-3,6-di(thiophen-2-yl)diketopyrrolo[3,4-c]pyrrole-1,4-dione-alt-thieno[3,2-b]thiophene) (DPPT-TT) polymer semiconductor based on a conjugated polymer/elastomer phase separation-induced elasticity (CONPHINE) structure. Unlike most previous studies on fully stretchable thin-film transistors (TFTs), which primarily report overall performance changes under mechanical strain, this work systematically identifies the dominant origin of electrical performance degradation through a stepwise electrical analysis encompassing the gate insulating layer, the semiconductor layer, and complete devices. Bottom-gate top-contact (BGTC) and bottom-gate bottom-contact (BGBC) devices were fabricated on rigid Si/SiO₂ substrates to examine the intrinsic properties of the DPPT-TT/styrene-ethylene-butylene-styrene (SEBS) CONPHINE film. As a result, the device exhibits 90% mobility retention even at 100% tensile strain applied parallel to the charge transport direction. Quantitative resistance analysis using the Y-function method reveals that variations in channel resistance play a dominant role in strain-induced performance degradation, whereas changes in contact resistance contribute only marginally. These findings demonstrate that stabilizing channel resistance, rather than contact resistance, is important for achieving high mobility retention under large mechanical deformation, thereby providing concrete and quantitative design guidelines for reliable stretchable TFTs. Full article

EPDM is widely used as the polymer matrix for solid rocket motor (SRM) internal thermal protection because of its low density, chemical inertness, and ability to form carbonaceous residue. Practical performance is frequently limited by weak char integrity and barrier properties, char oxidation, mechanical stripping in gas-dynamic flow, and by the poor comparability of published results due to non-uniform test conditions and reporting. This review systematizes studies on 0D nanofillers in EPDM ablatives and harmonizes the key metrics, including linear and mass ablation rates (LAR, MAR), back-face temperature (T_back), and solid residue yield. The major 0D additives-nSiO₂, nTiO₂, nZnO, and carbon black (CB) are compared, and their dominant mechanisms are summarized: degradation-layer structuring, reduced gas permeability, thermo-oxidative stabilization, and effects on vulcanization. Several studies report larger improvements for hybrid systems, where CB enhances char cohesion and retention, while oxide nanoparticles improve barrier performance and resistance to oxidation. Finally, an application-oriented selection matrix is proposed that accounts for thermal protection efficiency, processability, agglomeration limits, and density penalties to support EPDM coating design and improve comparability. Full article

Advanced oxidation processes using porphyrin-based heterogeneous catalysts hold promise for removing hazardous pollutants from wastewater. Their high visible-light absorption coefficients enable absorption of light from the solar spectrum. Moreover, their conjugated aromatic skeletons and intrinsic electronic properties facilitate the delocalization of photogenerated electrons during photodegradation. Delaying the recombination of photogenerated electron–hole pairs by introducing specific materials increases efficiency, as separated charges have more time to participate in redox reactions, boosting photocatalytic activities. However, applying these photocatalysts for wastewater treatment is challenging owing to facile agglomeration, deactivation, and recovery of the photocatalyst for reuse, which can significantly increase the overall cost. Therefore, new photocatalytic systems comprising porphyrin molecules must be developed. For this purpose, porphyrins can be conjugated to nanomaterials to create hybrid materials with photocatalytic efficiencies superior to those of free-standing starting porphyrins. Various transition metal oxides (TiO₂, ZnO, and Fe₃O₄) nanoparticles, main-group-element oxides (Al₂O₃ and SiO₂) nanoparticles, metal plasmons (silver nanoparticles), carbon-based platforms (graphene, graphene oxide, and g-C₃N₄), and polymer matrices have been used as nanostructured solid supports for the successful fabrication of porphyrin-conjugated hybrid materials. The conjugation of porphyrin molecules to solid supports improves the photocatalytic degradation activity in terms of visible-light conversion ability, recyclability, active porous sites, substrate mobility, separation of photogenerated charge species, recovery for reuse, and chemical stability, along with preventing the generation of secondary pollution. This review discusses the ongoing development of porphyrin-conjugated hybrid nanomaterials for the heterogeneous photocatalytic degradation of organic dyes, pharmaceutical pollutants, heavy metals, pesticides, and human care in water. Several important results and advancements in the field allow for a more efficient wastewater remediation process. Full article

The plasma-catalytic conversion of CO₂ is a promising route toward sustainable fuel and chemical production under mild operating conditions. However, many aspects still need to be better understood to improve performance and better understand the catalyst-plasma synergies. Among them, one aspect concerns understanding whether photons emitted by plasma discharges could induce changes in the catalyst, thereby promoting interaction between plasma species and the catalyst. This question was addressed by investigating the CO₂ splitting reaction in a planar dielectric barrier discharge (pDBD) reactor using titania-based catalysts that simultaneously act as discharge electrodes. Four systems were examined feeding pure CO₂ at different flow rates and applied voltage: bare titanium gauze, anodically formed TiO₂ nanotubes (TiNT), TiNT decorated with Ag–Au nanoparticles (TiNTAgAu), and TiNT supporting Ag–Au nanoparticles coated with polyaniline (TiNTAgAu/PANI). The TiNTAgAu exhibited the highest CO₂ conversion (35% at 10 mL min⁻¹ and 5.45 kV) and the most intense optical emission, even in the absence of external light irradiation, suggesting that the improvement is primarily attributed to plasma–nanoparticle interactions and self-induced localized surface plasmon resonance (si-LSPR) rather than conventional photocatalytic pathways. SEM analyses indicated severe plasma-induced degradation of TiNT and TiNTAgAu surfaces, leading to performance decay over time. In contrast, the TiNTAgAu/PANI catalyst retained structural integrity, with the polymeric coating mitigating plasma etching while maintaining competitive efficiency. There is thus a complex behavior with catalytic performance governed by nanostructure stability, plasmonic enhancement, and the interfacial protection. The results demonstrate how integrating plasmonic nanoparticles and conductive polymers can enable the rational design of durable and efficient plasma-photocatalysts for CO₂ valorization and other plasma-assisted catalytic processes. Full article

Perfluorosulfonic acid (PFSA) membranes suffer from severe conductivity decay caused by dehydration at elevated temperatures, hindering their application in medium- to high-temperature proton exchange membrane fuel cells (MHT-PEMFCs). To address this, Nafion/SiO₂ composite membranes with systematically varied filler contents were fabricated via a sol–gel-assisted casting strategy to enhance hydration stability and proton transport. Spectroscopic and microscopic analyses reveal a homogeneous nanoscale dispersion of SiO₂ within the Nafion matrix, along with strong interfacial hydrogen bonding between SiO₂ and sulfonic acid groups. These interactions effectively suppress polymer crystallinity and stabilize hydrated ionic domains. Thermogravimetric analysis confirms markedly improved water retention in the composite membranes at intermediate temperatures. Proton conductivity measurements at 50% relative humidity (RH) identify the Nafion/SiO₂-3 membrane as exhibiting optimal transport behavior, delivering the highest conductivity of 61.9 mS·cm⁻¹ at 120 °C and significantly improved conductivity retention compared to Nafion 117. Furthermore, single-cell tests under MHT-PEMFC conditions (120 °C, 50% RH) demonstrate the practical efficacy of these membrane-level enhancements, with the Nafion/SiO₂-3 membrane exhibiting an open-circuit voltage and peak power density 11.2% and 8.9% higher, respectively, than those of pristine Nafion under identical MEA fabrication and operating conditions. This study elucidates a clear structure–property–transport relationship in SiO₂-reinforced PFSA membranes, demonstrating that controlled inorganic incorporation is a robust strategy for extending the operational temperature window of PFSA-based proton exchange membranes toward device-level applications. Full article

In an effort to reduce global dependence on fossil-based polymers and advance toward a more sustainable materials industry, research over recent decades has increasingly focused on the development of bio-based polymers and broadening their potential applications. Within this context, the present study investigates nanocomposites based on poly(butylene succinate-co-butylene adipate) (PBSA), reinforced with two types of nanofillers: silicon dioxide nanoparticles (SiO₂ NPs) and cellulose nanofibrils (CNFs). The main objective of this work is to examine how the morphology, geometry, and chemical nature of the nanofillers influence the thermal, mechanical, and barrier properties of PBSA, as well as its biodegradability. For each nanofiller, three formulations were prepared, containing 1, 2, and 5 wt% of filler, respectively. Scanning electron microscopy (SEM) analysis confirmed good dispersion and minimal aggregation in the SiO₂-based systems, whereas marked aggregation was observed in the CNF-based samples. Thermal analysis indicated that the intrinsic thermal properties of neat PBSA were largely preserved. Mechanical testing revealed improvements in both the elastic modulus and elongation at break for most nanocomposite samples. In particular, CNFs provided the most consistent reinforcing effect, with enhancements of approximately 40% in the elastic modulus (495.4 vs. 356.4 GPa in neat PBSA) and 52% in elongation at the break (185.1 vs. 122.0% in neat PBSA) with 5 wt% loading. Additionally, the incorporation of nanofillers did not alter the surface hydrophilicity, but it did improve the oxygen barrier performance and enhanced disintegration under composting conditions. Overall, these findings demonstrate the promising potential of PBSA-based nanocomposites for sustainable rigid packaging applications. Full article

Advanced ceramics are known for their lightweight, high-temperature resistance, corrosion resistance, and biocompatibility. They are crucial in energy conversion, environmental protection, and aerospace fields. This review highlights the recent advancements in ceramic matrix composites, high-entropy ceramics, and polymer-derived ceramics, alongside various fabrication techniques such as three-dimensional printing, advanced sintering, and electric-field-assisted joining. Beyond the fabrication process, we emphasize how different processing methods impact microstructure, transport properties, and performance metrics relevant to catalysis. Additive manufacturing routes, such as direct ink writing, digital light processing, and binder jetting, are discussed and normalized based on factors such as relative density, grain size, pore architecture, and shrinkage. Cold and flash sintering methods are also examined, focusing on grain-boundary chemistry, dopant compatibility, and scalability for catalyst supports. Additionally, polymer-derived ceramics (SiOC, SiCN, SiBCN) are reviewed in terms of their catalytic performance in hydrogen evolution reaction, oxygen evolution reaction, oxygen reduction reaction, and CO₂ reduction reaction. CeO₂-ZrO₂ composites are particularly highlighted for their use in environmental catalysis and high-temperature gas sensing. Furthermore, insights on the future industrialization, cross-disciplinary integration, and performance improvements in catalytic applications are provided. Full article

Spent mushroom substrate (SMS)-derived bio-based polyurethane coatings typically exhibit poor hydrophobicity and short nutrient release durations, limiting their ability to satisfy long-term crop requirements. This study developed improved controlled-release urea by preparing water-repellent and compact bio-polymer coatings from recyclable SMS using non-toxic siloxane and nano-SiO₂ modifiers through simple processes. The dual modification markedly reduced water absorption (from 6.60% to 4.43%) and porosity (from 6.32% to 3.92%), creating a dense coating with lotus-leaf-like nanoscale surface protrusions and fewer intermembrane pores. As a result, the nitrogen (N) release period of the dual-modified bio-polymer-polyurethane-coated urea (SBPCU) with a 7% coating thickness was extended from 23 days to 42 days. Phytotoxicity assessments confirmed the excellent biosafety of the bio-polymer coating, revealing no adverse effects on maize growth and even promotional effects at low concentrations. This approach offers a sustainable, eco-friendly, and scalable strategy for producing bio-polymer-coated urea from agricultural waste, serving as a viable alternative to petrochemical coatings while improving nutrient use efficiency and biosafety. Full article

Understanding the role of carrier traps in the determination of dielectric breakdown of polymer nanocomposite would yield a novel method for the estimation of breakdown strength of the material. In this study, we propose a novel approach to predict the DC breakdown strength of polyethylene (PE) and its nanocomposite at room temperature via the bipolar charge transport (BCT) model based on trap energy estimated from isothermal surface potential decay (ISPD). Test specimens of polyethylene (PE) and its nanocomposites, with a thickness of 110 μm, were fabricated using the hot-pressing method by incorporating 20 nm SiO₂ particles as fillers. The distribution of carrier traps within these specimens was subsequently determined through ISPD measurements. The intrinsic breakdown strength of the sample was derived from the determined trap energy levels, by which the breakdown strength was predicted through the BCT model. Experimental DC breakdown tests were conducted on the specimens to validate the accuracy of the predictions. The results indicated that the DC breakdown strength predicted theoretically was in good agreement with that measured from the experiment. Such a prediction method provides a possible way to employ a non-destructive test to evaluate the DC breakdown strength of polymer nanocomposite. Full article

Low-melting bioabsorbable polymers, such as poly(caprolactone-co-lactide) (PCLA), hold significant promise for biomedical applications. However, achieving high-precision micro- and nanotopographical functionalization remains a formidable challenge due to the material’s susceptibility to thermal deformation during conventional thermal molding processes. In this study, functional microstructured PCLA coatings were engineered via low-temperature nanoimprint lithography utilizing a TiO₂–SiO₂ gas-permeable mold. These molds were synthesized via a sol–gel method utilizing titanium dioxide and silicon precursors. The gas-permeable nature of the mold facilitated the efficient evacuation of trapped air and volatiles during the imprinting process, enabling the high-fidelity replication of microstructures (1.3 μm height, 3 μm pitch) and nanostructured PCLA coatings featuring linewidths as narrow as 600 nm. The resultant microstructured PCLA coatings demonstrated modulated surface wettability, evidenced by an increase in water contact angles from 70.1° to 91.4°, and exhibited enhanced FD4 elution kinetics. These results confirm morphology-driven functionalities, specifically hydrophobicity and controlled release capabilities. Collectively, these findings underscore the efficacy of this microfabrication approach for polycaprolactone-based materials and highlight its potential to catalyze the development of high-value-added biomaterials for advanced medical and life science applications. This study establishes a foundational framework for the practical deployment of next-generation bioabsorbable materials and is anticipated to drive innovation in precision medical manufacturing. Full article

Bioactive glasses (BGs) are promising materials for enamel remineralization and caries management due to their ion-releasing ability and capacity to promote apatite formation. However, their clinical translation remains limited. Conventional BGs, such as 45S5, exhibit excellent bioactivity but are mechanically weak, prone to rapid ion burst release, and lack long-term stability. Recent advances—including secondary oxide incorporation (e.g., B₂O₃, ZnO), polymer–glass hybrids, and nanostructured systems like mesoporous BGs and RegeSi have improved reactivity, mechanical performance, and remineralization depth, though their durability under oral conditions is not yet established. BGs also display antibacterial activity by elevating local pH and releasing ions that inhibit cariogenic bacteria, but their broader ecological impact on the oral microbiome remains poorly understood. Emerging approaches such as halogen-modified BGs, particularly fluoride- and chloride-doped formulations, show dual benefits for remineralization and antimicrobial action, though supporting evidence is largely confined to in vitro studies. The absence of standardized protocols for assessing remineralization, ion release, and biofilm interaction further complicates cross-study comparisons and slows clinical adoption. Future progress will require interdisciplinary collaboration, standardized evaluation methods, and rigorous clinical validation to ensure that next-generation BGs can be safely and effectively integrated into dental practice. Full article

This study presents a new ternary copolymer synthesized via aqueous free-radical polymerization from sodium humate, sodium 2-methylprop-2-ene-1-sulfonate (SMAS), and 2-acrylamido-2-methylpropane sulfonic acid (AMPS). The resulting highly water-soluble, three-dimensional porous copolymer is complexed with aluminum sulfate to form a composite admixture containing AlO(OH), which acts as a highly effective accelerator for cement hydration. This system significantly shortens the initial and final setting times to averages of 2.62 min and 4.53 min, respectively, and enhances early-age mechanical strength (1.7 MPa compressive, 1.4 MPa flexural at 6 h). These improvements are correlated with the formation of key crystalline phases, including Al₂Si₂O₅(OH)₄ and Ca₃Al₂O₆·xH₂O gel. Incorporation of 50-mesh carbon fibers further reduces setting times (2.21 min initial, 3.93 min final) and increases 24 h strength (5.2 MPa compressive, 2.7 MPa flexural), despite a slight reduction in early strength (at 6 h). In contrast, 200-mesh carbon fibers extend the initial setting time and diminish early strength, associated with the formation of less effective gel phases such as Ca₃Al₂O₆·xH₂O, (CaO)_x(Al₂O₃)₁₁, and Ca₄Al₂O₇·xH₂O. Among these, the Al₂Si₂O₅(OH)₄ phase demonstrates superior performance, while finer carbon fibers show limited effectiveness in bridging hydration products. Conventionally employed as retarders or reinforcing agents, humate-based polymers and carbon fibers are shown here to function as dual-functional admixtures—serving as efficient setting accelerators while enhancing mechanical properties through tailored material design. This strategy offers a promising pathway for developing advanced multifunctional cement admixtures. Full article

Three new Cu(II) coordination polymers with 4,4′-bipyridine (bpy) were synthesized by hydrothermal reactions and their structures determined by single crystal X-ray diffraction. [Cu(bpy)₃(H₂O)₂](bpy)(PF₆)₂(H₂O)₃ (1) is built from bpy-bridged chains, [Cu(bpy)₂(H₂O)₂](bpy)(PF₆)₂(H₂O)₆ (2) from layers, and in [Cu(bpy)₂(NO₃)](bpy)(PF₆)₂(H₃O)(H₂O) (3) the layers are further connected by nitrate to a cuboid lattice. The magnetic properties of 3 are compared to [Cu(bpy)₂(H₂O)₂](SiF₆) (4) and [Cu(pyz)(bpy)(H₂O)₂](PF₆)₂ (5), where pyz = pyrazine. 3–5 are weakly coupled two-dimensional S = 1/2 antiferromagnetic Heisenberg lattices with 0.86 K < J < 1.47 K. Full article

In this work, novel biomass-derived carbon dots (CDs) with superior fluorescent properties were prepared from tomato straws. A selective, eco-friendly tetracycline (TC) sensor was fabricated by immobilizing a SiO₂ molecularly imprinted polymer (MIP) layer onto CDs, forming a CDs@SiO₂-MIP composite. This sensor combined highly selective adsorption properties with the sensitivity of fluorescence detection, with the sensing mechanism stemming from the off-fluorescent signal after molecular imprinting specifically recognizing the target substance. Under optimal conditions, the sensor exhibited a linear response to TC concentrations ranging from 1.00 × 10⁻⁷ to 5.00 × 10⁻⁴ mol/L, with fluorescence intensity decreasing as concentration increased. The detection limit of TC was 9.33 × 10⁻⁸ mol/L. This work provides novel biomass-derived CDs and a simple molecularly imprinted fluorescence sensing method for the detection of environmental organic pollutants. Full article