Core-shell Composites Research Articles

Polypyrrole-bismuth tungstate/polypyrrole core-shell for optoelectronic devices exhibiting Schottky photodiode behavior.

A polypyrrole-bismuth tungstate (Ppy-Bi2WO6) core-shell nanocomposite (n-type material) has been developed on a layered Ppy (p-type) base as an efficient light-capturing material exhibiting photodiode behavior. This device demonstrates promising sensitivity for light sensing and captures across a broad spectral range, from near IR to UV. The Bi2WO6/Ppy nanocomposite boasts an optimal bandgap of 2.0eV, compared to 3.4eV for Ppy and 2.5eV for Bi2WO6. The crystalline size of the core-shell composite is approximately 21nm, emphasizing its photon absorption capabilities. The composite particles, around 100nm in length, feature a highly porous morphology that effectively traps incident photons. The performance of this optoelectronic device is evaluated using current density (J) measurements under light (Jph) and dark (Jo) conditions. In darkness, the n-p type semiconductor exhibits limited current with a Jo of -0.22mA cm-2 at 2.0V. When exposed to white light, the Ppy- Bi2WO6/Ppy device generates hot electrons, achieving a Jph value of 1.1mA/cm-2 at 2.0V. It shows a superior responsivity (R) of 6.6mA/W at 340nm, gradually decreasing to 6.3mA/W at 440nm and 4.2mA/W at 540nm, indicating high sensitivity across the UV-Vis spectrum. At 730nm, the R-value is 2.6mA/W, highlighting its sensitivity in the near IR region. Additionally, at 340nm, the device achieves a detectivity (D) value of 0.15 × 10¹⁰ Jones, which decreases with longer wavelengths to 0.14 × 10¹⁰ Jones at 440nm, 0.9 × 10⁹ Jones at 540nm, and 0.63 × 10⁹ Jones at 730nm. With its great stability, low cost, easy fabrication, and potential for mass production, this optoelectronic light sensor and photodiode device holds significant promise for industrial applications as a highly effective optoelectronic device.

Inflammation-Responsive Functional Core-Shell Micro-Hydrogels Promote Rotator Cuff Tendon-To-Bone Healing by Recruiting MSCs and Immuno-Modulating Macrophages in Rats.

Rotator cuff injuries often necessitate surgical intervention, but the outcomes are often unsatisfactory. The underlying reasons can be attributed to multiple factors, with the intricate inflammatory activities and insufficient presence of stem cells being particularly significant. In this study, an innovative inflammation-responsive core-shell micro-hydrogel is designed for independent release of SDF-1 and IL-4 within a single delivery system to promote tendon-to-bone healing by recruiting MSCs and modulating M2 macrophages polarization. First, a MMP-2 responsive hydrogel loaded with IL-4 (GelMA-MMP/IL-4) is synthesized by cross-linking gelatin methacrylate (GelMA) with MMP-2 substrate peptide. Then, the resulting core particles are coated with a shell of chitosan /SDF-1/hyaluronic acid (CS/HA/SDF-1) using the layer-by-layer electrostatic deposition method to form a core-shell micro-hydrogel composite. The core-shell micro-hydrogel shows sustained release of SDF-1 and MMP-2-responsive release of IL-4 associated in situ MSCs homing and smart inflammation regulation by promoting M2 macrophages polarization. Additionally, by injecting these micro-hydrogels into a rat rotator cuff tear and repair model, notable improvements of fibrocartilage layer are observed between tendon and bone. Notably, this study presents a new and potentially powerful environment-responsive drug delivery strategy that offers valuable insights for regulating the intricate micro-environment associated with tissue regeneration.

Spatial Confinement Growth Enabling MoS2@Hollow Mesoporous Carbon Spheres Microspheres with Enhanced Microwave Absorption and Corrosion Resistance.

The complex electromagnetic applications in harsh corrosive environments urgently require research into multifunctional microwave absorption (MA) materials. The core-shell structure is an effective strategy to prepare multifunctional MA materials by efficiently combining the advantages of each component. Nevertheless, it remains a tough challenge to elucidate the effect of the binding positions of each component in MA materials on the comprehensive electromagnetic performance. Herein, two types of core-shell structured composites based on hollow mesoporous carbon spheres (HMCS), HMCS@MoS2 and MoS2@HMCS, were prepared via synergistic etch growth and spatial confinement growth strategies, respectively. Compared with HMCS, HMCS@MoS2 severely destroys the connection of HMCS, therefore resulting in impedance mismatching. Comparatively, the growth of MoS2 within the HMCS reduces the disruption of the HMCS connection, enabling MoS2@HMCS with enhanced dielectric loss while optimizing the impedance matching, and therefore, it yields an optimal reflection loss of -46.91 dB at 2 mm and an effective bandwidth of 5.78 GHz at 2.4 mm mixed with polydimethylsiloxane (PDMS). In addition, the combinations of the spatial confinement effect of HMCS, corrosion resistance of MoS2, and chemical stability of PDMS resulted in minimal changes in the MA performance of MoS2@HMCS/PDMS after soaking in acidic and alkaline solutions for 14 days, proving an excellent corrosion resistance property. This inspiring work proposes an effective spatial confinement growth strategy to optimize the impedance matching and further tailor the multifunction for dielectric loss dominated MA materials.

Synthesis and Characterization of Submicron Spherical Core-Shell High-Energy Composites via Electrospray Method

In this study, submicron spherical core-shell high-energy composites of RDX/F2311@CuO/Al were synthesized using the electrospray method. The results demonstrate that the combustion time of composite high-energy microspheres, prepared via electrospraying, was significantly reduced to 460.0 ms from an original 2296.0 ms observed in samples prepared by physical mixing. Additionally, the flame burning was more concentrated, and the combustion process exhibited greater stability. Additionally, the flame combustion exhibited greater concentration and the overall combustion process was more stable. Furthermore, by manipulating the proportion of non-energy-containing components, it is possible to obtain composites with adjustable combustion rates. By manipulating the ratio of aluminium thermal agent, it is possible to procure a composite material with a more vigorous combustion process, thereby enabling the functional modulation of said composite material. Compared to the raw material RDX, the H50 value of the composite microspheres has increased from 14.49cm to 25.16cm, indicating a significant enhancement in impact resistance along with a remarkable desensitization effect. Additionally, the explosion percentage of the composite microspheres has been reduced from 84% to 68%. These significant desensitization effects highlight the morphological advantages of the core-shell structure and the synergistic reaction energy benefits of the components involved.

Silica-Based Composite Sorbents for Heavy Metal Ions Removal from Aqueous Solutions.

Weak polyelectrolyte chains are versatile polymeric materials due to the large number of functional groups that can be used in different environmental applications. Herein, one weak polycation (polyethyleneimine, PEI) and two polyanions (poly(acrylic acid), PAA, and poly(sodium methacrylate), PMAA) were directly deposited through precipitation of an inter-polyelectrolyte coacervate onto the silica surface (IS), followed by glutaraldehyde (GA) crosslinking and extraction of polyanions chains. Four core-shell composites based on silica were synthesized and tested for adsorption of lead (Pb2+) and nickel (Ni2+) as model pollutants in batch sorption experiments on the laboratory scale. The sorbed/desorbed amounts depended on the crosslinking degree of the composite shell, as well as on the type of anionic polyelectrolyte. After multiple loading/release cycles of the heavy metal ions, the maximum sorption capacities were situated between 5-10 mg Pb2+/g composite and 1-6 mg Ni2+/g composite. The strong crosslinked composites (r = 1.0) exhibited higher amounts of heavy metal ions (Me2+) sorbed than the less crosslinked ones, with less PEI on the surface but with more flexible chains being more efficient than more PEI with less flexible chains. Core-shell composites based on silica and weak polyelectrolytes could act as sorbent materials, which may be used in water or wastewater treatment.

Preparation of 3D Zonal and Interactional Glomerular Models Based on Composite Core–Shell Hydrogel Microspheres

Preparation of 3D Zonal and Interactional Glomerular Models Based on Composite Core–Shell Hydrogel Microspheres

Synthesis of UiO-66-NH2@PILs core-shell composites for CO2 conversion into cyclic carbonates via synergistic catalysis under solvent- and additive-free conditions

Metal-organic frameworks (MOFs) have been hybridized with other functional materials, such as ionic liquids, covalent organic frameworks (COFs), and metallic nanoclusters, to fabricate composite materials. These composites possess the structural characteristics of their individual components and exhibit synergistic properties. In this work, we demonstrate the synthesis of core-shell structure UiO-66-NH2@PILs-x composite materials by encapsulating MOFs within ionic polymers (PILs) with varying thicknesses of PILs shell. These hybrid materials serve as bifunctional catalysts for the conversion of CO2 into cyclic carbonates under solvent- and additive-free conditions through a synergistic catalytic effect facilitating the conversion of CO2 into cyclic carbonates under solvent- and additive-free conditions through synergistic catalytic effect, exhibiting superior catalytic performance and excellent recyclability. This MOFs-based composite material provides a competitive approach for CO2 catalytic conversion.

Sintering Driven Void Formation in PS@WO3 Core-Shell Composites: A Photodegradation Enhancement Strategy

Background: Polystyrene nanospheres are used as a substrate for the hydrothermal coating of tungsten trioxide (WO3) to form a core-shell composite of PS@WO3. The core-shell structure is used for the next sintering step. This produces porous WO3. The focus of this study is on the role of porous WO3 in enhancing photocatalytic performance. Methods: The hydrothermal method was employed for coating, and the surface morphology, as well as the structural properties of WO3-coated PS spheres, were systematically investigated using SEM and XRD analyses. Additionally, the sintering process was introduced to enhance the material by inducing rupture in the PS sphere core, creating voids that significantly increased the material's surface area. Results: The evaluation of the effect of sintering temperature on photodegradation efficiency highlighted the crucial role of sintering temperature. Un-sintered and 300°C sintered WO3, both having a hexagonal crystalline structure, exhibited superior degradation efficiencies compared to samples sintered at higher temperatures (400°C and 500°C). In particular, the 300°C sintered WO3 outperformed its un-sintered counterpart despite identical crystalline structures. The performance of the PS@WO3 composite was assessed to determine the enhanced role of porous WO3. The porous WO3 obtained, in particular by the sintering of the core-shell PS@WO3 composites at 300°C, showed a remarkable improvement in the degradation efficiency. These composite demonstrated over 95% efficiency within 10 minutes and achieved near complete (100%) degradation for a further 10 minutes, surpassing the performance of pure WO3. It is important to clarify that while the final product was predominantly WO3 after the sintering process, the inclusion of PS served a critical purpose in creating voids during sintering. The PS@WO3 composite structure used as a resource for the preparation of porous WO3, even with a potentially reduced PS composition, has been found to play a significant role in influencing the surface area of the material, and consequently the photocatalytic performance. Conclusion: The study has highlighted the importance of crystalline structure and sintering conditions in optimizing the efficiency of photocatalytic materials. The porous WO3 obtained, in particular by the sintering of the core-shell PS@WO3 composites at 300°C, showed promising potential for applications under UV and visible LED light irradiation. These results provide valuable insights for the development of advanced photocatalytic materials with improved performance, highlighting WO3 as the key contributor to the observed improvements.

Fabrication of core-shell structural Y@VTMS-DVB composites with enhanced hydrophobicity for toluene capture under humid environment

Zeolite Y serves as an effective adsorbent for VOCs capture due to its ordered porous structure, exceptional thermal stability, chemical resistance and fine-tune key properties. However, the hydrophilicity caused by the low SiO2/Al2O3 ratio seriously limits its industrial application, especially in humid environments. In this work, a series of core-shell composites Y@VTMS-DVBn were prepared through surface grafting and copolymerization. A variety of characterizations were utilized to study the structural and morphological changes of the prepared samples. The dynamic breakthrough adsorption experiment showed that the toluene uptake was significantly improved from 1.77 mg/g to 53.09 mg/g under 30 % relative humidity. Moreover, the core-shell composite exhibited excellent regeneration properties, the adsorption capacity remained 90 % under wet conditions after 6 cycles of regeneration. Adsorption kinetic analysis revealed that the adsorption behavior of toluene on the prepared adsorbents was primarily physical adsorption. These results show that the core-shell composite is a promising candidate for VOCs removal in industrial application.

Influence of Chitosan on the Viability of Encapsulated and Dehydrated Formulations of Vegetative Cells of Actinomycetes.

This study focuses on developing an encapsulated and dehydrated formulation of vegetative actinobacteria cells for an efficient application in sustainable agriculture, both as a fungicidal agent in crop protection and as a growth-stimulating agent in plants. Three strains of actinobacteria were used: one from a collection (Streptomyces sp.) and two natives to agricultural soil, which were identified as S3 and S6. Vegetative cells propagated in a specific liquid medium for mycelium production were encapsulated in various alginate-chitosan composites produced by extrusion. Optimal conditions for cell encapsulation were determined, and cell damage from air-drying at room temperature was evaluated. The fresh and dehydrated composites were characterized by porosity, functional groups, size and shape, and their ability to protect the immobilized vegetative cells' viability. Actinomycetes were immobilized in capsules of 2.1-2.7 mm diameter with a sphericity index ranging from 0.058 to 0.112. Encapsulation efficiency ranged from 50% to 88%, and cell viability after drying varied between 44% and 96%, depending on the composite type, strain, and airflow. Among the three immobilized and dried strains, S3 and S6 showed greater resistance to encapsulation and drying with a 4 L·min-1 airflow when immobilized in coated and core-shell composites. Encapsulation in alginate-chitosan matrices effectively protects vegetative actinobacteria cells during dehydration, maintaining their viability and functionality for agricultural applications.

Oxygen vacancies enhancing hierarchical NiCo2S4@MnO2 electrode for flexible asymmetric supercapacitors

The limited energy density of supercapacitors hampers their widespread application in electronic devices. Metal oxides, employed as electrode materials, suffer from low conductivity and stability, prompting extensive research in recent years to enhance their electrochemical properties. Among these efforts, the construction of core–shell heterostructures and the utilization of oxygen vacancy (VO) engineering have emerged as pivotal strategies for improving material stability and ion diffusion rates. Herein, core–shell composites comprising NiCo2S4 nanospheres and MnO2 nanosheets are grown in situ on carbon cloth (CC), forming nanoflower clusters while introducing VO defects through a chemical reduction method. Density functional theory (DFT) results proves that the existence of VO effectively enhances electronic and structural properties of MnO2, thereby enhancing capacitive properties. The electrochemical test results show that NiCo2S4@MnO2-V3 exhibits excellent 1376 F g−1 mass capacitance and 2.06 F cm−2 area capacitance at 1 A g−1. Moreover, NiCo2S4@MnO2-V3//activated carbon (AC) asymmetric supercapacitor (ASC) can achieve an energy density of 39.7 Wh kg−1 at a power density of 775 W kg−1, and maintains 15.5 Wh kg−1 even at 7749.77 W kg−1. Capacitance retention is 73.1 % after 10,000 cycles at 5 A g−1, and coulombic efficiency reaches 100 %, demonstrating satisfactory cycle stability. In addition, the device’s excellent flexibility offers broad application prospects in wearable electronic applications.

S vacancies and heterojunction modulated MoS2/C@Fe3O4 towards improved full-spectrum photo-Fenton catalysis: Enhanced interfacial charge transfer and NIR absorption

Fe3O4-based core–shell/heterojunction composites exhibit favorable photothermal catalytic performance in environmental remediation, but limited by the weak interface electron transport efficiency and poor near infrared (NIR) absorption capacity. Herein, Sv-MoS2/C@Fe3O4 core–shell composites were prepared for the first time by coating S vacancies-bearing MoS2 (Sv-MoS2) on the surface of carbon-decorated Fe3O4 microspheres (C@Fe3O4) derived from copper slag-based polymer microspheres and was used as photothermal catalyst to activate H2O2 towards chlortethromycin hydrochloride (CTC) elimination from wastewater. By virtue of the synergistic effect of the petal-like Sv-MoS2, carbon-decorated layer and multi light reflection in porous microspheres, Sv-MoS2/C@Fe3O4 exhibited excellent full spectrum absorption and carrier migration efficiency, with catalytic activity of 0.149 min−1 and H2O2 utilization rate of 93.6 %. The degradation rate is 3.9 and 3.1 times of C@Fe3O4 and MoS2/C@Fe3O4 under full light irradiation which can heat the solution from room temperature to 72.4 °C. This excellent catalytic performance is mainly originated from that the S-type heterostructure promotes the charge separation, transfer and redox ability, and enhances catalytic oxidation by regulating electron density of the interfacial carbon and reducing the energy barrier of H2O2 activation through S vacancies. Moreover, the decorated carbon layer can serve as a hot core to provide heat to Sv-MoS2 and enhance the collision chance of photogenerated carriers, thus improving the catalytic performance of Sv-MoS2/C@Fe3O4. This work provides new strategies for constructing heterojunction materials with fast electron transport efficiency and using solar energy for environmental remediation.

Copper stearate-coated DAP-4 core–shell composites for enhanced safety and thermal decomposition performance

In this study, DAP-4@copper stearate (CS) core–shell composites were fabricated by an in situ synthesis and liquid deposition using CS as the catalyst. In addition, a comprehensive characterization was conducted on the morphology, structure, thermal decomposition, and safety performance of the acquired samples. The results revealed that DAP-4@CS composites with a complete, compact core–shell structure. During thermal analysis experiments, DAP-4@CS (5, 10, 15, and 20 wt%) resulted in a reduction in the thermal decomposition peak temperatures (Tp) by 35.22, 55.02, 68.22 and 73.76 °C respectively when compared with DAP-4, and their corresponding activation energy values decreased by 61.22, 87.3, 63.62, and 69.54 kJ/mol. Notably, the DAP-4@CS composites with 5 wt% and 10 wt% CS exhibited increased heat release by 1291.03 and 1546.8 J/g, respectively. The H50 value for DAP-4 increased from an initial value of 44.67 cm to an improved value of 64.57 cm, while its friction sensitivity increased from 30 N to 40 N during safety experiments. Moreover, we propose the principle of thermal decomposition catalysis and desensitization of CS for DAP-4. The above research results provide a new solution to the contradictions and obstacles in the application of DAP-4 as an oxidizer in fuel.

Control of burning rate pressure sensitivity for solid propellants by changing the interfacial contact of Al/HMX/AP with precisely located graphene-based energetic catalysts

The control of burning rate pressure sensitivity is essential for stable and reliable combustion of solid propellants. It has been proved that the combustion behavior of propellants can be effectively tuned by interfacial control of Al/oxidizers. In this work, core-shell Al-based composites, using oxidizers such as ammonium perchlorate (AP) and cyclotetramethylene tetranitramine (HMX) as the shell layer, have been prepared with a well-controlled location of graphene-based carbohydrazide complexes (GO-CHZ-M, M = Co2+ or Ni2+) as the catalysts. The catalysts can be located inside HMX or embedded on the surface of AP particles. The decomposition of AP and HMX could be greatly promoted with a trace amount of catalyst. Under the synergistic effects of Al/oxidizer interfacial control and GO-CHZ-M, the ignition delay time is shortened by >48 % with increased in flame radiation. More importantly, the burning rate (r) and pressure exponent (n) of the solid propellants are effectively regulated in a wide range. In particular, the use of Al@HMX/Co results in a lowered n of 0.29 within 1∼20 MPa compared to 0.79 for the blank reference sample. The agglomeration of Al particles during combustion was also inhibited due to the micro-explosion effect of Al@HMX composites. Novelty and Significance statementThe innovative approaches of integrating Al/HMX/AP composites and precise catalysis of graphene-based energetic catalysts in solid propellants have successfully achieved, regarding the modulation of the burning rates and pressure sensitivity. Moreover, the effect of catalyst location on the ignition delay and burning rates has also been studied thoroughly and clarified. This paper provides new insight into the regulation of combustion performance of solid propellants, with improved reaction efficiency and maintained energy density.

3D-Printed (CoCrFeMnNi)3O4@C-GR dual core–shell composites: Multilevel control and mechanisms of microwave absorption performance

With the rapid development of modern electronic technology, there is an increasing demand for microwave-absorbing materials in various applications. These include reducing electromagnetic interference, enhancing communication quality, and ensuring stealth capabilities for military equipment. This study has developed a novel microwave-absorbing material, which is a composite system consisting of a high-entropy dual-core–shell (CoCrFeMnNi)3O4@C combined with graphene (GR), and is composed of polylactic acid (PLA) as the matrix. The material is prepared through a process involving high-temperature oxidation, carbonization to form the shell, and Powder extrusion molding techniques. The results demonstrate that when the dual-core–shell (CoCrFeMnNi)3O4@C microspheres are added at a loading of 20 wt%, and GR is added at 7 wt%, with a thickness of 2.22 mm, the composite material achieves a minimum reflection loss (RLmin) value of −51.36 dB and an effective absorption bandwidth (EAB) of 5.20 GHz. This excellent performance is attributed to the lattice distortion, a large number of oxygen vacancies, and abundant heterogeneous interfaces and conductive networks within the composites. These factors work together to stimulate multiple relaxation mechanisms, enhance the magnetic loss effect, and greatly improve the microwave absorption capability. The introduction of high-entropy microspheres effectively modulates the high conductivity of GR, further enhancing the comprehensive absorption performance of the material. This study not only offers a new strategy for designing and preparing high-performance microwave-absorbing materials but also establishes a valuable scientific foundation for materials research and application in related fields.

Room temperature synthesis of a chiral covalent organic framework core-shell composite for high-performance liquid chromatography enantioseparation.

In this article, chiral covalent organic framework core-shell composite CCOF-TpPa-Py@SiO2 was facilely synthesized by induction at room temperature. The CCOF-TpPa-Py@SiO2 core-shell composite was used as a chiral stationary phase for the separation of the racemates by high-performance liquid chromatography, which exhibits good separation performance for chiral compounds including ketones, alcohols, esters, epoxides, carboxylic acids, amides, and amines. The effects of analyte injection mass on the enantioseparation were studied. The reproducibility and stability of the CCOF-TpPa-Py@SiO2 chiral column were explored. The intra-day (n=5), inter-day (n=5), and inter-column (n=3) relative standard deviations for the migration times and resolution of benzoin were 0.32%-0.54%, 0.45%-0.61%, and 1.21%-1.53%, respectively. In addition, the chiral separation ability of the CCOF-TpPa-Py@SiO2 chiral column (column A) was compared with that of the MDI-β-CD-Modified COF@SiO2 (column B) as well as a commercial chiral column (Chiralpak AD-H). The chiral recognition ability of column A is complementary to that of column B and AD-H column. The resolution mechanism of CCOF-TpPa-Py@SiO2 stationary phase towards chiral analyte was explored. Hence, the synthesis of CCOF-TpPa-Py@SiO2 core-shell composite by induction at room temperature as chiral stationary phases for chromatographic separation has important research potential and application prospects.

Double emulsion templates for efficient production of phase change microcapsules

The utilization of phase change materials (PCMs) in thermal storage technology exhibits great potential for various applications in thermal management and latent heat storage systems. However, leakage of organic PCMs hinders its practical application. Encapsulation of PCMs in microcapsules with polymer shells can prevent PCM leakage while improving heat transfer and stability. In this study, shell monomers were introduced as an immiscible third phase into the traditional o/w two-phase emulsion system, and the formed three-phase complex emulsion was dynamically reconfigured to exhibit a core–shell encapsulated conformation induced by interfacial tension, resulting in the formation of a thermodynamically stable double emulsion. Microcapsules with 1,6-hexanediol diacrylate (HDDA) shells were successfully prepared using this double emulsion as a template. The emulsion configuration is of significant advantage in promoting stable encapsulation of the phase change material in the shell material, resulting in fast and efficient encapsulation and improved utilization of the phase change material. Phase change microcapsules with different phase change temperatures were prepared and characterized using n-octadecane (C18), methyl stearate (Mes), n-eicosane (C20) and n-docosane (C22) as phase change materials, respectively. Results show that the prepared microcapsules are spherically integrated, with smooth surfaces and obvious core–shell structures, and the enthalpies of phase transition of C18, Mes, C20 and C22 microcapsules are as high as 171.86, 122.37, 165.77 and 178.69 J/g, respectively. These microcapsules exhibit excellent thermal stability and durability and the encapsulation efficiencies exceed 99.7 % at different phase change temperatures. Furthermore, the potential applications of PCM microcapsules in the field of temperature regulation were also demonstrated. This double-emulsion template method provides a straightforward, rapid and scalable approach for the mass production of microcapsules with different core–shell compositions.

Highly stable carbon-coated nZVI composite Fe0@RF-C for efficient degradation of emerging contaminants

Nanoscale zerovalent iron (nZVI) has garnered significant attention as an efficient advanced oxidation activator, but its practical application is hindered by aggregation and oxidation. Coating nZVI with carbon can effectively addresses these issues. A simple and scalable production method for carbon-coated nZVI composite is highly desirable. The anti-oxidation and catalytic performance of carbon-coated nZVI composite merit in-depth research. In this study, a highly stable carbon-coated core-shell nZVI composite (Fe0@RF-C) was successfully prepared using a simple method combining phenolic resin embedding and carbothermal reduction. Fe0@RF-C was employed as a heterogeneous persulfate (PS) activator for degrading 2,4-dihydroxybenzophenone (BP-1), an emerging contaminant. Compared to commercial nZVI, Fe0@RF-C exhibited superior PS activation performance and oxidation resistance. Nearly 95% of BP-1 was removed within 10 min in the Fe0@RF-C/PS system. The carbon layer promotes the enrichment of BP-1 and accelerates its degradation through singlet oxygen oxidation and direct electron transfer processes. This study provides a straightforward approach for designing highly stable carbon-coated nZVI composite and elucidates the enhanced catalytic performance mechanism by carbon layers.

Preparation of nitrogen-doped reduced graphene oxide/zinc ferrite@nitrogen-doped carbon composite for broadband and highly efficient electromagnetic wave absorption

Traditionally reduced graphene oxide (RGO)-based electromagnetic wave (EMW) absorbing materials have poor absorption effectiveness due to impedance mismatch caused by skin effect. The introduction of structural defects and the design of heterogeneous interfaces play a crucial role in enhancing the polarization effect of EMW absorbers. In this study, nitrogen-doped reduced graphene oxide/zinc ferrite@nitrogen-doped carbon (NRGO/ZnFe2O4@NC) ternary composite with rich heterogeneous interfaces is constructed by combining solvothermal reaction, in-situ polymerization, annealing treatment with subsequent hydrothermal reaction. The research results have shown that the obtained NRGO/ZnFe2O4@NC ternary composite exhibits a unique core-shell structure and excellent EMW absorption performance. At a thickness of 2.61 mm, the maximum effective absorption bandwidth can reach 7.2 GHz, spanning the entire Ku-band and a portion of the X-band, and the minimum reflection loss is –61.1 dB, which is superior to most reported RGO-based EMW absorbers. The excellent EMW absorbing ability is mainly ascribed to the optimized impedance matching and the enhanced polarization loss caused by the abundant heterogeneous interfaces and structural defects derived from heteroatomic nitrogen doping. Furthermore, the radar cross section in the far field is simulated by a computer simulation technique. This study provides a novel way to prepare core-shell magnetic carbon composites as highly efficient and broadband EMW absorbers.

Synthesis, characterization of FeNi3@SiO2@CuS for enhance solar photocatalytic degradation of atrazine herbicides: Application of RSM

This study was focused on the response surface methodology modeling (RSM) for the removal of Atrazine residue (ATZ) using nanocomposite. The FeNi3@SiO2@CuS nanocomposite was fabricated by co-precipitation and sol-gel methodologies, and their properties were studied by XRD, FTIR, VSM, and SEM techniques. The synthesis core-shell composite was used to degrade atrazine herbicide (ATZ) from synthetic wastewater. The efficiency of FeNi3@SiO2@CuS was calculated as a function of different input parameters (pH, ATZ concentration, catalyst concentration, H2O2 concentration, and reaction time by using a central composite design (CCD) adapted from response surface methodology. The CCD created a matrix of 60 runs of the experiment to look into how the five input elements interacted with one another. A reduced quadratic model was created using the findings and demonstrated good predictability of outcomes consistent with the research findings. Variance analysis (ANOVA) indicated that the chosen model was highly significant (p < 0.0001), and the coefficients of determination R2, adjusted R2, and predicted R2 were 0.9587, 0.9513, and 0.9380, respectively, confirming that the second-order regression model had been satisfactorily adjusted to obtained data. Furthermore, the findings provide validation that the degradation rate of ATZ adheres to a pseudo-first-order kinetic model, exhibiting an impressive R2 value surpassing 0.98. Through the use of a numerical optimization technique, a 95.24 % ATZ elimination was represented by the desirability of 81.12 %. This study suggests that sunlight, catalyst, and H2O2 together have a significant influence on ATZ degradation. Additionally, RSM was an appropriate process for optimizing the factors related to the elimination of ATZ by a solar-induced photocatalytic process.