Search Results (229)

The sludge produced by the Fenton process contains mixed-valence iron particulates (hereafter called Fenton wastes). Using a solvothermal method, we fabricated a new heterogeneous photo-Fenton catalyst using Fenton wastes and metal–organic frameworks (MOFs). Nanoporous metal carboxylate (MIL-88) MOF impregnated with Fenton waste was functionalized using 2,5-dihydroxyterephthalic acid (x-HO-MIL-88-C, x, concentration of the 2,5-dihydroxyterephthalic acid). The efficiency of x-HO-MIL-88-C was examined under visible light radiation using methylene blue (MB) as an index pollutant. We observed the best catalytic performance for MB degradation by 4-HO-MIL-88-C. In the photo-Fenton process, the simultaneous presence of singlet oxygen, superoxide, and hydroxyl radicals is confirmed by free radical quenching and electron spin resonance spectral data. These free radicals associate with holes in the non-selective degradation of MB. The 4-HO-MIL-88-C catalyst shows good stability and reusability, maintaining over 80% efficiency at the end of five consecutive cycles. This work opens up a new path for recycling Fenton wastes into usable products. Full article

This study presents the successful fabrication of lead zirconate titanate (PZT) thin films on silicon (Si) substrates using a hybrid deposition method combining spin-coating and RF sputtering techniques. Initially, a PZT layer was deposited through four successive spin-coating cycles, followed by an additional layer formed via RF sputtering. The resulting multilayer structure was annealed at ${700 }^{°}$C for 2 h to improve crystallinity. Comprehensive material characterization was conducted using XRD, SEM, cross-sectional SEM, EDX, and UV–VIS absorbance spectroscopy. The analyses confirmed the formation of a well-crystallized perovskite phase, a uniform surface morphology, and an optical band gap of approximately 3.55 eV, supporting its suitability for sensing applications. Building upon these findings, a multilayer PZT-based touch sensor was fabricated and electrically characterized. Low-frequency I–V measurements demonstrated consistent and repeatable polarization behavior under cyclic loading conditions. In addition, $\left|Z\right|$–f measurements were performed to assess the sensor’s dynamic electrical behavior. Although expected dielectric responses were observed, the absence of distinct anti-resonance peaks suggested non-idealities linked to ${\mathrm{Ag}}^{+}$ ion diffusion from the electrode layers. To account for these effects, the classical Butterworth–Van Dyke (BVD) equivalent circuit model was extended with additional inductive and resistive components representing parasitic pathways. This modified model provided excellent agreement with the measured impedance and phase data, offering deeper insight into the interplay between material degradation and electrical performance. Overall, the developed sensor structure exhibits strong potential for use in piezoelectric sensing applications, particularly for tactile and pressure-based interfaces. Full article

The textile industry generates a large amount of waste, producing approximately 92 million tons of textile waste annually, much of which ends up in landfills. This alarming figure highlights the need for an urgent waste management strategy. Mechanical recycling has emerged and is being explored as an alternative to manage this waste, enabling the transformation of discarded textiles into recycled fibers for the production of new materials. In this study, a Life Cycle Assessment (LCA) was conducted for five different knitted fabrics, considering the origin of their cotton content: from virgin cotton to post-industrial and post-consumer recycled cotton fibers, to evaluate the environmental impact of each fabric. The analysis revealed that the spinning, dyeing, and finishing processes were the primary contributors across multiple environmental impact categories. Specifically, for the Water Scarcity Potential (WSP) indicator, these processes accounted for 96% of the total impact. In terms of raw material contributions to water scarcity, organic cotton fiber had the highest impact at 54%, followed by post-consumer recycled cotton at 24% and post-industrial recycled cotton at 22%. Variations in environmental contributions were also observed for the remaining impact categories. A key challenge in this study is the lack of a dedicated impact category in LCA that directly quantifies the environmental benefits of using recycled materials. Specifically, current LCA methodologies do not have a standardized metric to measure the impact reduction achieved by substituting virgin fibers with recycled ones, even though comparisons indicate reduced impacts. Full article

This study focused on the preparation of poly(ε-caprolactone)/carbon nanotubes (PCL/CNTs) composite membranes via electrospinning technology and investigated their performance in oil–water separation. The effects of varying CNTs contents and spinning parameters on the structure and properties of the membrane materials were systematically studied. A highly uniform diameter distribution of the PCL fiber was achieved by using the dichloromethane/dimethylformamide (DCM/DMF) composite solvent with volume ratio of 7:3, as well as a PCL concentration of ca. 17 wt.%. The optimal electrospinning parameters were identified as an applied voltage of 18 kV and a syringe pump flow rate of 1 mL·h⁻¹, which collectively ensured uniform fiber morphology under the specified processing conditions. The critical threshold concentration of CNTs in the composite system was determined to be 1 wt.%, above which the composite fibers exhibit a significant increase in diameter heterogeneity. Both pristine PCL fibrous membranes and PCL/CNTs composite membranes demonstrated excellent and stable oil–water separation performance, with separation efficiencies consistently around 90%. Notably, no significant attenuation in separation efficiency was observed after ten consecutive separation cycles. Furthermore, when incorporating 0.5 wt.% CNTs, the PCL/CNT composite membranes exhibited a 20% increase in separation flux for heavy oils compared to pristine PCL membranes. Additionally, CNTs, as a prototypical class of nanofillers for polymer matrix reinforcement, can potentially enhance the mechanical properties of composite films, thus effectively prolonging their service life. Full article

This study presents a systematic approach to engineering the electron transport layer (ETL) in perovskite solar cells using a spray deposition technique to fabricate sequentially compact and mesoporous titanium dioxide (c-TiO₂, m-TiO₂) films. The spray coating method leads to the development of a distinct reticulated morphology characterized by well-defined wavy-like surface features and significantly increased roughness—at least twice that of spin-coated mesoporous films. The increased interfacial area between the mesoporous TiO₂ and the perovskite layer facilitates more efficient charge transfer, contributing to higher device performance. By optimizing the deposition parameters, particularly the number of spray cycles for the m-TiO₂ layer, we achieve a significant enhancement in device performance, with improvements in power conversion efficiency (PCE), reduced series resistance, and minimized hysteresis. Our results demonstrate that an optimal film thickness promotes better perovskite anchoring, while excessive deposition impedes light transmission and increases sheet resistance. These findings advance the practical fabrication of high-performance perovskite solar cells using simple solution-processing techniques and highlights the potential of scalable spray deposition methods for industrial-scale fabrication. Full article

Exploring advanced sulfur cathode materials is important for the development of lithium-sulfur batteries (LSBs), but they still present challenges. Herein, zinc oxide dots-modified vanadium nitride flower-like heterojunctions (Zn-QDs-VN) as sulfur hosts are prepared by a phase separation strategy. Characterizations confirm that the flower structure with high specific surface area and pores improves active site exposure and electron/mass transfer. In situ phase separation enriches the Zn-QDs-VN interface, addressing the issues of uneven distribution and interface reduction of Zn-QDs-VN. Further theoretical computations reveal that ZnO-QDs-VN with optimized intermediate spin states can constitute a stable LiS* bond sequence, which can conspicuously facilitate the adsorption and conversion of LiPSs and reduce the battery reaction energy barrier. Therefore, the ZnO-QDs-VN@S cathode shows a high initial specific capacity of 1109.6 mAh g⁻¹ at 1.0 C and long cycle stability (maintaining 984.2 mAh g⁻¹ after 500 cycles). Under high S loading (8.5 mg cm⁻²) and lean electrolyte conditions (E/S = 6.5 μL mg⁻¹), it also exhibits a high initial area capacity (10.26 mAh cm⁻²) at 0.2 C. The interfacial synergistic effect accelerates the adsorption and conversion of LiPSs and reduces the energy barriers in cell reactions. The study provides a new method for designing heterojunctions to achieve high-performance LSBs. Full article

Current hydrogels used for cartilage tissue engineering often lack the mechanical strength and structural integrity required to mimic native human cartilage. This study addresses this limitation by developing reinforced hydrogels based on a ternary polymer blend of poly(vinyl) alcohol (PVA), gelatin (GL), and chitosan (CH), with gentamicin sulfate (GS) as an antimicrobial agent and a crosslinker. The hydrogels were produced using two crosslinking methods, the freeze/thaw and heated cycles, and reinforced with forcespun polycaprolactone (PCL) nanofiber to improve mechanical performance. Chemical characterization revealed that GS forms weak hydrogen bonds with the ternary polymers, leading to esterification with PVA, and covalent bonds are formed as the result of the free amino group (-NH₂) of chitosan that reacts with the carboxylic acid group (-COOH) of gelatin. SEM images help us to see how the hydrogels are reinforced with polycaprolactone (PCL) fibers produced via force spinning technology, while mechanical properties were evaluated via uniaxial tensile and compressive tests. Water retention measurements were performed to examine the crosslinking process’s influence on the hydrogel’s water retention, while the hydrogel surface roughness was obtained via confocal microscopy images. A constitutive model based on non-Gaussian strain energy density was introduced to predict experimental mechanical behavior data of the hydrogel, considering a non-monotonous softening function. Loading and unloading tests demonstrated that GS enhanced crosslinking without compromising water retention or biocompatibility because of the reaction between the free amino group of CH and the carboxylic group of gelatin. The PCL-reinforced PVA/GL/CH hydrogel shows strong potential for cartilage repair and tissue engineering applications. Full article

To address the challenge of abatement of volatile organic compounds (VOCs) in environmental catalysis, this study developed a temperature-gradient hydrothermal strategy to fabricate SrSn(OH)₆ nanocatalysts and systematically investigatd their photocatalytic performance and mechanisms for gaseous toluene degradation. SrSn(OH)₆ (SSH) was synthesized via a simple hydrothermal method with optimal preparation conditions identified as a reaction temperature of 140 °C and duration of 12 h. The crystallinity of SrSn(OH)₆ was modulated by adjusting the pH of the precursor solution, yielding materials with distinct morphologies, specific surface areas, and band gaps. The narrowed band gap of SrSn(OH)₆ nanocatalysts facilitated electron excitation to generate additional photogenerated electron-hole pairs. The SSH-10.5 sample with ordered planar and hole-like structures promoted carrier migration, effectively suppressed electron-hole recombination, and enhanced the conversion of abundant surface hydroxyl groups into hydroxyl radicals. Under UV irradiation, SSH-10.5 achieved a toluene degradation efficiency of 69.56% and showed excellent stability after five reuse cycles. Electron spin resonance analysis confirmed the presence of •OH and •O₂⁻ radicals in the reaction system, with •OH identified as the dominant active species. In situ FT-IR spectroscopy revealed that •OH and •O₂⁻ radicals attacked the methyl group of toluene, converting it into intermediates including benzyl alcohol, benzaldehyde, and benzoic acid. This work provides a novel design of high-efficiency VOC-photocatalytic materials and shows significant implications for advancing industrial exhaust gas purification technologies. Full article

Addressing the issues of poor thermal resistance in conventional polyolefin separators and the low production efficiency of electrospinning, this study innovatively employed high-efficiency centrifugal spinning technology to fabricate a ternary blended modified fiber membrane composed of polyacrylonitrile (PAN), polystyrene (PS), and polymethyl methacrylate (PMMA). By precisely adjusting the polymer ratio (8:2:2) and fine-tuning the spinning process parameters, a separator with a three-dimensional network structure was successfully produced. The research results indicate that the separator exhibited excellent overall performance, with a porosity of 75.87%, an electrolyte absorption rate of up to 346%, and a thermal shrinkage of less than 3% after 1 h at 150 °C, along with a tensile strength reaching 23.48 MPa. A lithium-ion battery assembled with this separator delivered an initial discharge capacity of 159 mAh/g at a 0.2 C rate and maintained a capacity retention of 98.11% after 25 cycles. Moreover, under current rates of 0.5, 1.0, and 2.0 C, the battery assembled with the ASM-14 configuration achieved high discharge capacities of 148, 136, and 116 mAh/g, respectively. This study offers a novel design strategy for modifying multi-component polymer battery separators. Full article

Hydrogen chloride (HCl) is one of the most hazardous air pollutants and can cause significant damage to human health and the environment. Therefore, the continuous quantitative monitoring of HCl is of great practical importance. In this work, a novel triphenylamine derivative, named TPTc-DBD, with a Schiff base structure was synthesized. The molecular structure of TPTc-DBD was determined by NMR analysis, FTIR analysis and single crystal diffraction analysis. On this basis, a porous polyvinylidene fluoride (PVDF) film containing TPTc-DBD was then prepared by a spin-coating method, and its sensitivity to HCl was evaluated by naked eye and ultraviolet-visible absorption spectrum, respectively. The detection limit of the composite porous film for HCl molecules was determined to be 5.8 mg/m³. Interestingly, the composite films absorbing HCl can be reactivated by NH₃, which provides a cycle detection ability for HCl. After five testing cycles, the detection error remained below 1%. Furthermore, the microstructure of the film remained unchanged, highlighting its exceptional detection performance for HCl. Full article

As a rarefied metallic element, strontium (Sr) is susceptible to significant environmental radioactive contamination risks during industrial mining and refining processes. In this study, NaA molecular sieves were prepared by alkali excitation using synthetic powders, which were homogeneously blended with the polyacrylonitrile (PAN) matrix, and nanoscale TiO₂ reinforcing phases were introduced. Finally, composite separation membranes (TiO₂-NaA@PANMs) with stable adsorption properties were constructed by electrostatic spinning technology. The micro-morphology and interfacial properties were characterized by SEM, XRD, and FT-IR systems. The adsorption experiments demonstrated that the equilibrium adsorption capacity of the system for Sr²⁺ reached 55.00 mg/g at the optimized pH = 6.0, and the theoretical saturated adsorption capacity at 298 K was 80.89 mg/g. The isothermal process conformed to the Langmuir’s model of monomolecular layer adsorption, and the kinetic behavior followed the quasi-secondary kinetic equation. Following three cycles of regeneration by elution with a 0.3 mol/L sodium citrate solution, the membrane material exhibited 81.60% Sr²⁺ removal efficacy. The composite membrane passages exhibited remarkable potential for utilization in engineering applications involving the treatment of complex nuclear wastewater. Full article

Gold nanoparticles–cuprous oxide/reduced graphene oxide/polypyrrole (AuNPs-Cu₂O/rGO/PPy) hybrid nanocomposites were synthesized for surface acoustic wave (SAW) sensors, achieving high sensitivity (2 Hz/ppb), selectivity, and fast response (~2 min) at room temperature. The films, deposited via spin-coating, were characterized by SEM, EDS, and XRD, revealing a rough, wrinkled morphology beneficial for gas adsorption. The sensor showed significant frequency shifts to NH₃, enhanced by AuNPs, Cu₂O, rGO, and PPy. It had a 6.4-fold stronger response to NH₃ compared to CO₂, H₂, and CO, confirming excellent selectivity. The linear detection range was 12–1000 ppb, with a limit of detection (LOD) of 8 ppb. Humidity affected performance, causing negative frequency shifts, and sensitivity declined after 30 days due to resistivity changes. Despite this, the sensor demonstrated excellent NH₃ selectivity and stability across multiple cycles. In simulated breath tests, it distinguished between healthy and patient-like samples, highlighting its potential as a reliable, non-invasive diagnostic tool. Full article

In recent years, transition metal oxides (TMOs) have emerged as promising candidates for anode materials in lithium-ion batteries (LIBs) owing to their high theoretical capacities. Regrettably, most TMOs exhibit poor electronic/ionic conductivity and undergo substantial volume expansion during the lithiation/delithiation processes. In this study, an electrostatic spinning method using polyacrylonitrile, graphene, and iron(III) acetylacetonate as precursors was employed to synthesize the Fe₃O₄@G/C composite through carbon coating and graphene doping. The composition, phase structure, and morphology of the Fe₃O₄@G/C composite were thoroughly investigated. The electrochemical performance of the Fe₃O₄@G/C composite as a lithium-ion battery anode was evaluated through a continuous charge–discharge cycling test. After 100 cycles at a current density of 0.1 A/g, the specific capacity of the Fe₃O₄@G/C material remained at 595.8 mAh/g. Additionally, the incorporation of graphene leads to a reduction in the electron orbital energy of Fe, which was verified by comparing the density of states (DOS) before and after the doping. Simultaneously, the electrochemical performance of CoO@G/C and NiO@G/C composites further demonstrates that doping transition metal oxides with graphene can enhance their performance as anodes for lithium-ion batteries. We anticipate that this design concept will open new avenues for the development of transition metal oxides (TMOs) and propel their adoption in practical applications. Full article

Polyphenols are organic molecules extracted from various fruits, such as coffee and citrus, that possess biological activity and antioxidant properties. However, the presence of polyphenols in the environment is hazardous to water quality and living health. Among a variety of water remediation methods, adsorption remains a staple in the field. Therefore, this work aims to develop porous polycaprolactone: poly(methyl methacrylate) (PCL:PMMA) membranes as a support for hydrotalcite immobilization for the removal of chlorogenic acid polyphenol (CGA) from aqueous solutions. Due to the hydrophilic nature of hydrotalcite, the adsorbent was functionalized with hexadecyltrimethylammonium bromide (CTAB) to increase its affinity for CGA, resulting in a removal efficiency of approximately 96%. Composite fiber membranes were prepared by solution-blowing spinning with specific amounts of hydrotalcite added (i.e., 1 to 60 wt%). A 3:1 PCL:PMMA blend resulted in superior mechanical traction (0.8 MPa) and stress deformation (70%) compared to pure PCL (0.7 MPa and 37%) and PMMA (0.1 MPa and 5%) fibers. PCL:PMMA membranes with 60% LDH-CTAB exhibited CGA removal rates equal to 55% in the first cycle while maintaining the capacity to remove 30% of the polyphenol after five consecutive reuses. Removal rates up to 90% could also be achieved with an appropriate adsorbent dose (2 g L⁻¹). Adsorption was found to follow pseudo-second-order kinetics and was adequately described by the Langmuir model, saturating LDH-CTAB active sites in four hours. PCL:PMMA:LDH-CTAB composites can be considered a potential alternative to support adsorbents for water remediation. Full article

In this paper, a composite separator for lithium-ion batteries was successfully prepared by electrostatic spinning, based on polyacrylonitrile (PAN) and 5% cellulose nanocrystals (CNCs) derived from sisal fiber. Its physical and electrochemical properties as well as the enhanced mechanism were investigated. The obtained 5%CNCs/PAN separator offers an excellent thermal stability, ultra-high electrolyte uptake (486 ± 30%), high ionic conductivity (2.82 mS cm⁻¹ at 25 °C) and a wide electrochemical window (5.3 V). In addition, a lithium-ion battery assembled with the 5%CNCs/PAN separator can work stably for 1000 h at 5 mA cm⁻². The CNCs in the electrolyte enable the immobilization of PF₆⁻, thereby inhibiting the migration of anions and increasing its Li⁺ transfer number (t_Li⁺) to 0.75, which is 65.3% higher than that of a pure PAN separator. The battery with the 5%CNCs/PAN separator retains 97.4% of its initial reversible capacity after 100 cycles, which is much higher than that of a pure PAN separator, with a value of 62.9%. These results suggest the potential utility of 5%CNCs/PAN separators as high-performance separators required in lithium-ion batteries. Full article