Search Results (486)

In this study we report on the structural, mechanical, and electrical characterization of different structures of vertically aligned zinc oxide (ZnO) nanowires (NWs) synthesized using hydrothermal methods. By optimizing the growth conditions, scanning electron microscopy (SEM) micrographs show that the ZnO NWs could reach an astounding 51.9 ± 0.82 µm in length, 0.7 ± 0.08 µm in diameter, and 3.3 ± 2.1 µm⁻² density of the number of NWs per area within 24 h of growth time, compared with a reported value of ~26.8 µm in length for the same period. The indentation modulus of the as-grown ZnO NWs was determined using contact resonance (CR) measurements using atomic force microscopy (AFM). An indentation modulus of 122.2 ± 2.3 GPa for the NW array sample with an average diameter of ~690 nm was found to be close to the reference bulk ZnO value of 125 GPa. Furthermore, the measurement of the piezoelectric coefficient (d₃₃) using the traceable ESPY33 tool under cyclic compressive stress gave a value of 1.6 ± 0.4 pC/N at 0.02 N with ZnO NWs of 100 ± 10 nm and 2.69 ± 0.05 µm in diameter and length, respectively, which were embedded in an S1818 polymer. Current–voltage (I-V) measurements of the ZnO NWs fabricated on an n-type silicon (Si) substrate utilizing a micromanipulator integrated with a tungsten (W) probe exhibits Ohmic behavior, revealing an important phenomenon which can be attributed to the generated electric field by the tungsten probe, dielectric residue, or conductive material. Full article

Chronic wounds pose a great challenge due to their slow healing and susceptibility to infections, hence the need for innovative alternatives to conventional antibiotics, as increasing bacterial resistance limits the efficacy of current treatments. This paper addresses the development of novel electrospun membranes based on polyvinyl alcohol (PVA) and sodium alginate, incorporating therapeutic ZnO and bioglass (54SiO₂:40CaO:6P₂O₅) nanoparticles. While nanocomposites presented smaller fiber diameters than pure polymers, ternary nanocomposites displayed higher values, e.g., in porous areas, values were in the ca. 80–240 nm range and 0.06–0.60 μm², respectively. The Young’s modulus of the PVA/SA membrane, initially 15.9 ± 2.0 MPa, decreased by 65% with 10 wt.% ZnO NPs, whereas 10 wt.% BG NPs increased it by 100%. The membranes demonstrated efficacy against Gram-positive bacteria, including methicillin-resistant Staphylococcus aureus (MRSA) isolated from a human wound secretion, as well as two ATCC strains: Staphylococcus aureus and Staphylococcus epidermidis. A cell viability assay conducted with HaCaT cells demonstrated nearly complete survival following 72 h of membrane exposure. Their combined Gram-positive antibacterial activity and cytocompatibility support their potential application as biofunctional dressings for the management of chronic and hospital-acquired topical infections, while also contributing to the global effort to combat antibiotic resistance. Full article

This study reports the development of a highly sensitive electrochemical sensor for phosphate ion detection, utilizing silicon nanowires (SiNWs) as the transducing elements and a novel copper (II) phthalocyanine-acrylate polymer adduct (Cu (II) Pc-PAA) as the functional sensing layer. Silicon nanowires were fabricated via metal-assisted chemical etching (MACE) with etching durations of 15, 25, 35, 45, and 60 min. The SiNWs etched for 15 min exhibited the highest sensitivity, showing superior electrochemical performance. Functionalized SiNWs were systematically evaluated for phosphate ion (HPO₄²⁻) detection over a wide concentration range (10⁻¹⁰ to 10⁻⁶ M) using Mott–Schottky measurements. The surface morphology of the SiNWs was thoroughly characterized before and after Cu (II) Pc-PAA layer functionalization. The sensing material was analyzed using contact angle goniometry and scanning electron microscopy (SEM), confirming both its uniform distribution and effective immobilization. The sensor displayed a Nernstian behavior with a sensitivity of 28.25 mV/Decade and an exceptionally low limit of detection (LOD) of 1.5 nM. Furthermore, the capacitive sensor exhibited remarkable selectivity toward phosphate ions, even in the presence of potentially interfering anions such as Cl⁻, NO₃⁻, SO₄²⁻ and ClO₄⁻. These results confirm the sensor’s high sensitivity, selectivity, and fast response, underscoring its suitability for environmental phosphate ion monitoring. Full article

Environmentally friendly coated urea prepared using a waterborne polymer coating material is essential for promoting green and sustainable practices in modern agriculture. However, significant efforts are still urgently needed to address the undesirable properties of waterborne polymer coatings, i.e., poor hydrophobic properties and numerous micropores. Herein, dual nano-SiO₂ and siloxane-modified waterborne-polymer-coated urea was successfully developed. The characteristics of waterborne-polymer-coated urea before and after modification were compared. The results demonstrate that nano-SiO₂ and siloxane modification improved the hydrophobicity (water absorption decreased from 119.86% to 46.35%) and mechanical strength (tensile strength increased from 21.09 to 31.29 MPa, and the elongation at break exhibited an increase of 22.42%) of the waterborne polymer coatings. Furthermore, the –OH number of the modified coatings was decreased, while the coating surface formed a nano-scale rough structure, prolonging the nitrogen (N)-controlled release period from 7 to 28 days. Overall, the proposed novel dual-modification technique utilizing waterborne polymer coatings highlights the significant potential of eco-friendly coated urea with renewable coatings in modern agriculture. Full article

Plastic waste accumulation is one of the most pressing environmental challenges of the 21st century, owing to the widespread use of synthetic polymers and the limitations of conventional recycling methods. Among available strategies, chemical upcycling via depolymerization has emerged as a promising circular approach that converts plastic waste back into valuable monomers and chemical feedstocks. This article provides an in-depth narrative review of recent progress in the upcycling of major plastic types such as PET, PU, PS, and engineering plastics through thermal, chemical, catalytic, biological, and mechanochemical depolymerization methods. Each method is critically assessed in terms of efficiency, scalability, energy input, and environmental impact. Special attention is given to innovative catalyst systems, such as microsized MgO/SiO₂ and Co/CaO composites, and emerging enzymatic systems like engineered PETases and whole-cell biocatalysts that enable low-temperature, selective depolymerization. Furthermore, the conversion pathways of depolymerized products into high-purity monomers such as BHET, TPA, vanillin, and bisphenols are discussed with supporting case studies. The review also examines life cycle assessment (LCA) data, techno-economic analyses, and policy frameworks supporting the adoption of depolymerization-based recycling systems. Collectively, this work outlines the technical viability and sustainability benefits of depolymerization as a core pillar of plastic circularity and monomer recovery, offering a path forward for high-value material recirculation and waste minimization. Full article

China has abundant shale oil and gas resources, which have become a critical pillar for future energy substitution. However, due to the highly heterogeneous nature and complex pore structures of shale reservoirs, traditional plugging agents face significant limitations in enhancing plugging efficiency and adapting to extreme wellbore environments. In response to the technical demands of nanoparticle-based plugging in shale reservoirs, this study systematically investigated the microscopic interaction mechanisms of nano-plugging agent shell polymers (Ployk) with various reservoir minerals under different temperature and salinity conditions using molecular simulation methods. Key parameters, including interfacial interaction energy, mean square displacement, and system density distribution, were calculated to thoroughly analyze the effects of temperature and salinity variations on adsorption stability and structural evolution. The results indicate that nano-plugging agent shell polymers exhibit pronounced mineral selectivity in their adsorption behavior, with particularly strong adsorption performance on SiO₂ surfaces. Both elevated temperature and increased salinity were found to reduce the interaction strength between the shell polymers and mineral surfaces and significantly alter the spatial distribution and structural ordering of water molecules near the interface. These findings not only elucidate the fundamental interfacial mechanisms of nano-plugging agents in shale reservoirs but also provide theoretical guidance for the precise design of advanced nano-plugging agent materials, laying a scientific foundation for improving the engineering application performance of shale oil and gas wellbore-plugging technologies. Full article

The interest in macromolecular alkoxysilyl-functionalized hybrids (self-assembling or nanostructured), which could be used as precursors in biomimetic silica precipitation and for the synthesis of hollow spherical silica particles, is growing. Nevertheless, reports on all-organosilicon systems for bioinspired silica precipitation are scarce. Therefore, a new kind of polyalkoxysilane macromonomer–linear polysilsesquioxane (LPSQ) of ladder-like backbone, functionalized in side chains with trimethoxysilyl groups (LPSQ-R-Si(OMe)₃), was designed following this approach. It was obtained by photoinitiated thiol-ene addition of 3-mercaptopropyltrimethoxysilane to the vinyl-functionalized polysilsesquioxane precursor, carried out in situ in tetraethoxysilane (TEOS). The mixture of LPSQ-R-Si(OMe)₃ and TEOS (co-monomers) was used in a sol–gel process conducted under acidic conditions (0.5 M HCl/NaCl) in the presence of Pluronic^® F-127 triblock copolymer as a template. LPSQ-R-Si(OMe)₃ played a key role for the formation of microparticles of a spherical shape that were formed under the applied conditions, while their size (as low as 3–4 µm) was controlled by the stirring rate. The hybrid materials were hydrophobic and showed good thermal and oxidative stability. Introduction of zinc acetate (Zn(OAc)₂) as an additive in the sol–gel process influenced the pH of the reaction medium, which resulted in structural reinforcement of the hybrid microparticles owing to more effective condensation of silanol groups and a relative increase of the content of SiO₂. The proposed method shows directions in designing the properties of hybrid materials and can be translated to other silicon–organic polymers and oligomers that could be used to produce hollow silica particles. The established role of various factors (macromonomer structure, pH, and stirring rate) allows for the modulation of particle morphology. Full article

As a key insulating material in power equipment, epoxy resins (EP) are often limited in practical applications due to space charge accumulation and mechanical degradation. This study systematically investigates the effects of SiO₂ nanoparticle doping on the electrical and mechanical properties of SiO₂/EP composites through molecular dynamics simulations and first-principles calculations. The results demonstrate that SiO₂ doping enhances the mechanical properties of EP, with notable improvements in Young’s modulus, bulk modulus, and shear modulus, while maintaining excellent thermal stability across different temperatures. Further investigations reveal that SiO₂ doping effectively modulates the interfacial charge behavior between EP and metals (Cu/Fe) by introducing shallow defect states and reconstructing interfacial dipoles. Density of states analysis indicates the formation of localized defect states at the interface in doped systems, which dominate the defect-assisted hopping mechanism for charge transport and suppress space charge accumulation. Potential distribution calculations show that doping reduces the average potential of EP (1 eV for Cu layer and 1.09 eV for Fe layer) while simultaneously influencing the potential distribution near the polymer–metal interface, thereby optimizing the interfacial charge injection barrier. Specifically, the hole barrier at the maximum valence band (VBM) after doping significantly increased, rising from the initial values of 0.448 eV (Cu interface) and 0.349 eV (Fe interface) to 104.02% and 209.46%, respectively. These findings provide a theoretical foundation for designing high-performance epoxy-based composites with both enhanced mechanical properties and controllable interfacial charge behavior. Full article

Polymers containing biocidal moieties (e.g., amino or ammonium groups) are considered promising materials that can help combat the growing resistance of pathogens to commonly used antimicrobials. Searching for new polymeric biocides, in this work, non-porous and porous poly(hydromethylsiloxane) (PHMS) networks were prepared and post-functionalized by N-allylaniline (Naa). Non-porous networks were obtained by cross-linking PHMS in the bulk and porous—in W/O high-internal-phase emulsion (HIPE). Linear divinyldisiloxane (M₂^Vi) or cyclic tetravinyltetrasiloxane (D₄^Vi) were used as cross-linkers. Studies confirmed the expected non-porous and open macroporous microstructure of the initial networks. They also showed that functionalization by Naa was more efficient for the non-porous networks that swelled to lower extents in toluene and contained higher amounts of Si-H groups than the porous ones. In the reactions with benzyl chloride or 1-bromoctane, some amino groups present in these materials were transformed to ammonium groups. It was found that activity against Gram-positive S. aureus and Gram-negative E. coli bacteria depended on the functionalization degree, cross-linking level and the microstructure of the modified materials. Full article

Mesoporous silicon dioxide films have been shown to be well suited as adhesion-promoting interlayers for generating high-strength polymer–metal interfaces. These films can be fabricated via microwave plasma-enhanced chemical vapor deposition using the precursor hexamethyldisiloxane and oxygen as working gas. The resulting mesoporous structures enable polymer infiltration during overmolding, which leads to a nanoscale form-locking mechanism after solidification. This mechanism allows for efficient stress transfer across the interface and makes the resulting adhesion highly dependent on the morphology of the deposited film. To gain a deeper understanding of the underlying deposition mechanisms and improve process stability, this work investigates the growth behavior of mesoporous silica films using a multiple regression analysis approach. The seven process parameters coating time, distance, chamber pressure, substrate temperature, flow rate, plasma pulse duration, and pause-to-pulse ratio were systematically varied within a Design of Experiments framework. The resulting films were characterized by their free surface area, mean agglomerate diameter, and film thickness using digital image analysis, white light interferometry, and atomic force microscopy. The deposited films exhibit a wide range of morphological appearances, ranging from quasi-dense to dust-like structures. As part of this research, the free surface area varied from 15 to 55 percent, the mean agglomerate diameter from 17 to 126 nm, and the film thickness from 35 to 1600 nm. The derived growth model describes the deposition process with high statistical accuracy. Furthermore, all coatings were overmolded via injection molding and subjected to mechanical testing, allowing a direct correlation between film morphology and their performance as adhesion-promoting interlayers. Full article

Stimuli-responsive polymers (SRPs) have garnered significant attention in recent decades due to their immense potential in biomedical and environmental applications. When these SRPs are grafted onto magnetic nanoparticles, they form multifunctional nanocomposites capable of various complex applications, such as targeted drug delivery, advanced separations, and magnetic resonance imaging. In this study, we employed a one-step hydrothermal method using 3-aminopropyltrimethoxysilane (APTES) to synthesize APTES-modified Fe₃O₄ nanoparticles (APTES@Fe₃O₄) featuring reactive terminal amine groups. Subsequently, via two consecutive surface-initiated atom transfer radical polymerizations (SI-ATRP), pH- and temperature-responsive polymer blocks were grown from the Fe₃O₄ surface, resulting in the formation of poly(itaconic acid)-block-poly(N-isopropyl acrylamide) (PIA-b-PNIPAM)-grafted nanomagnetic particles (PIA-b-PNIPAM@Fe₃O₄). To confirm the chemical composition and assess how the particle morphology and size distribution of these SRP-based nanocomposites change in response to ambient pH and temperature stimuli, various characterization techniques were employed, including transmission electron microscopy, differential light scattering, and Fourier transform infrared spectroscopy. The results indicated successful synthesis, with PIA-b-PNIPAM@Fe₃O₄ demonstrating sensitivity to both temperature and pH. Full article

In order to improve oil recovery efficiency in low-permeability reservoirs, this study developed amphiphilic Janus-SiO₂ nanoparticles to prepare polymer gel microspheres for enhanced oil recovery (EOR). Firstly, Janus-SiO₂ nanoparticles were synthesized via surface modification using (3-aminopropyl)triethoxysilane and α-bromoisobutyryl bromide. Fourier-transform infrared spectroscopy (FTIR) and scanning electron microscopy (SEM) characterization confirmed the successful grafting of amino and styrene chains, with the particle size increasing from 23.8 nm to 32.9 nm while maintaining good dispersion stability. The Janus nanoparticles exhibited high interfacial activity, reducing the oil–water interfacial tension to 0.095 mN/m and converting the rock surface wettability from oil-wet (15.4°) to strongly water-wet (120.6°), thereby significantly enhancing the oil stripping efficiency. Then, polymer gel microspheres were prepared by reversed-phase emulsion polymerization using Janus-SiO₂ nanoparticles as emulsifiers. When the concentration range of nanoparticles was 0.1–0.5 wt%, the particle size range of polymer gel microspheres was 316.4–562.7 nm. Polymer gel microspheres prepared with a high concentration of Janus-SiO₂ nanoparticles can ensure the moderate swelling capacity of the particles under high-temperature and high-salinity conditions. At the same time, it can also improve the mechanical strength and shear resistance of the microspheres. Core displacement experiments confirmed the dual synergistic effect of this system. Polymer gel microspheres can effectively plug high-permeability zones and improve sweep volume, while Janus-SiO₂ nanoparticles enhance oil displacement efficiency. Ultimately, this system achieved an incremental oil recovery of 19.72%, exceeding that of conventional polymer microsphere systems by more than 5.96%. The proposed method provides a promising strategy for improving oil recovery in low-permeability heterogeneous reservoir development. Full article

High permeance combined with high salt/dye separation efficiency is a prerequisite for achieving zero-liquid-discharge treatment of saline textile wastewater by membrane technology. Thin-film nanocomposite (TFN) membranes incorporating porous nanoparticles offer a promising route to overcome the permeability–selectivity trade-off of conventional polymer membranes. In this study, a vacuum-assisted method was used to co-blend ZIF-67 and SiO₂ nanoparticles, while branched polyethyleneimine (PEI) served as a cross-linking bridge, resulting in a high-performance TFN membrane for salt/dye separation. Acting as a molecular connector, PEI coordinated with ZIF-67 through metal–amine complexation and simultaneously formed hydrogen bonds with surface hydroxyl groups on SiO₂, thereby linking ZIF-67 and SiO₂. The resulting membrane exhibited good hydrophilicity and excellent dye separation performance (water flux = 359.8 L m⁻² h⁻¹ bar⁻¹; Congo Red rejection = 99.2%) as well as outstanding selectivity in dye/salt mixtures (Congo Red/MgCl₂ selectivity of 1094). The optimal ZIF@SiO₂-PEI membrane maintained stable dye rejection over a wide range of trans-membrane pressures, initial concentrations, and pH values. These results reveal the huge potential of applying the ZIF@SiO₂-PEI TFN membranes for resource recovery in sustainable textile wastewater systems. Full article

This study addresses the critical challenge of maintaining drilling fluid performance and wellbore stability in high-pressure, high-temperature (HPHT) environments, where conventional water-based drilling fluids often fail. This research investigates whether the integration of single- and dual-nanomaterial systems into base fluids can significantly enhance rheological behavior and shale inhibition potential. Using secondary experimental datasets and computational modeling, five nanomaterials—SiO₂, Al₂O₃, TiO₂, Fe₂O₃, and Fe₃O₄—were evaluated individually and in dual combinations with polymers. Key performance metrics, including plastic viscosity, fluid loss, and shale recovery, were analyzed and fitted to the Herschel–Bulkley rheological model. The results showed that single-nanomaterial systems modestly improved viscosity and fluid loss control, with SiO₂ and Fe₂O₃ offering the best standalone performance. Dual systems—particularly SiO₂–Al₂O₃ and Fe₃O₄–polymer combinations—demonstrated superior rheological performance with reduced viscosity (down to 19 cP), minimized fluid loss (<4 mL/30 min), and enhanced shale recovery (>90%). These improvements suggest synergistic effects between nanomaterials, supporting their use in designing advanced, thermally stable drilling fluids for extreme HPHT wells. Full article

Thermal Energy Storage (TES) technologies improve solar power dispatchability by addressing the important challenge of energy intermittency. Sensible heat energy storage technology using materials based on Ordinary Portland Cement (OPC) is the simplest and most economical. However, the operation of these materials is limited to temperatures below 400 °C due to the structural degradation of OPC at this temperature. This paper investigates the design and development of inorganic polymers based on Construction and Demolition Waste (CDW) as a sustainable, low-cost, and environmentally friendly alternative to OPC-based materials for high-temperature sensible TES applications. Based on the ternary systems Na₂O-SiO₂-Al₂O₃ and K₂O-SiO₂-Al₂O₃, representative compositions of CDW-based inorganic polymers were theoretically designed and evaluated using the thermochemical software FactSage 7.0. The experimental verification of the theoretically designed inorganic polymers confirmed that they can withstand temperatures higher than 500 and up to 700 °C. The optimized materials developed compressive strength around 20 MPa, which was improved with temperatures up to 500 °C and then decreased. Moreover, they presented thermal capacities from 600 to 1090 J kg⁻¹ °C ⁻¹, thermal diffusivity in the range of 4.7–5.6 × 10⁻⁷ m² s⁻¹, and thermal conductivity from 0.6 to 1 W m⁻¹ °C⁻¹. These properties render the developed inorganic polymers significant candidates for TES applications. Full article