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Thermoelectrics are an important class of materials with great potential in alternative energy applications. In this study, two-dimensional (2D) nanoplates of the layered chalcogenides, Sb2Te3 and Bi2Te3, are synthesized and composites of the two are investigated for their thermoelectric properties. The two materials, Sb2Te3 and Bi2Te3, were synthesized as hexagonal, 2D nanoplates via a colloidal polyol route. The as-synthesized Sb2Te3 and Bi2Te3 vary drastically from one another in their lateral and vertical dimensions as revealed by scanning electron microscopy and atomic force microscopy. The single crystalline nanoplate nature is deduced by high-resolution transmission electron microscopy and selected area electron diffraction. Nanoplates have well-defined hexagonal facets as seen in the scanning and transmission electron microscopy images. The nanoplates were consolidated as an anisotropic nanostructured pellet via spark plasma sintering. Preferred orientation observed in the powder X-ray diffraction pattern and scanning electron microscopy images of the fractured pellets confirm the anisotropic structure of the nanoplates. Thermoelectric properties in the parallel and perpendicular directions were measured, revealing strong anisotropy with a significant reduction to thermal conductivity in the perpendicular direction due to increased phonon scattering at nanoplate interfaces. All compositions, except that of the 25% Bi2Te3 nanoplate composite, behave as degenerate semiconductors with increasing electrical resistivity as the temperature increases. The Seebeck coefficient is also increased dramatically in the nanocomposites, the highest reaching 210 μV/K for 15% Bi2Te3. The increase in Seebeck is attributed to energy carrier filtering at the nanoplate interfaces. Overall, these enhanced thermoelectric properties lead to a drastic increase in the thermoelectric performance in the perpendicular direction, with zT ∼ 1.26, for the 15% Bi2Te3 nanoplate composite at 450 K.

Mineral-polymer composites found in nature exhibit exceptional structural properties essential to their function, and transferring these attributes to the synthetic design of functional materials holds promise across various sectors. Biomimetic fabrication of nanocomposites introduces new pathways for advanced material design and explores biomineralization strategies. This study presents a novel approach for producing single platelet nanocomposites composed of CaCO3 and biomimetic peptoid (N-substituted glycines) polymers, akin to the bricks found in the brick-and-mortar structure of nacre, the inner layer of certain mollusc shells. The significant aspect of the proposed strategy is the use of organic peptoid nanosheets as the scaffolds for brick formation, along with their controlled mineralization in solution. Here, we employ the B28 peptoid nanosheet as a scaffold, which readily forms free-floating zwitterionic bilayers in aqueous solution. The peptoid nanosheets were mineralized under consistent initial conditions (σcalcite = 1.2, pH 9.00), with variations in mixing conditions and supersaturation profiles over time aimed at controlling the final product. Nanosheets were mineralized in both feedback control experiments, where supersaturation was continuously replenished by titrant addition and in batch experiments without a feedback loop. Complete coverage of the nanosheet surface by amorphous calcium carbonate was achieved under specific conditions with feedback control mineralization, whereas vaterite was the primary CaCO3 phase observed after batch experiments. Thermodynamic calculations suggest that time-dependent supersaturation profiles as well as the spatial distribution of supersaturation are effective controls for tuning the mineralization extent and product. We anticipate that the control strategies outlined in this work can serve as a foundation for the advanced and scalable fabrication of nanocomposites as building blocks for nacre-mimetic and functional materials.

In recent times, there has been a pressing need to discover or manufacture a unique material that can serve as a photocatalyst for organic pollutants that are incapable of degradation. Pure Bi 2 O 3 and Co, Cd co-doped Bi 2 - 2x Co x Cd x O 3 (x = 0.8) nanoparticles were synthesized using the chemical co-precipitation method, but the new approach involves fabricating 10 % reduced graphene oxide Bi 2 - 2x Co x Cd x O 3 /rGO nanocomposites via the ultra-sonication route. This study investigated the effects of Co, Cd, and r-GO doping on the optical, electrochemical, structural, and photocatalytic properties of bismuth oxide. The synthesized nanomaterials were analyzed using X-ray diffraction (XRD), cyclic voltammetry, ultraviolet–visible (UV–Vis), Fourier transform infrared (FTIR), photoluminescence (PL), and Raman spectroscopy. The XRD patterns showed the formation of a monophasic monoclinic structure belonging to space group P21/c, with an average crystallite size estimated around 22–41 nm. According to the UV–visible study, the bandgap energy of Bi 2 O 3 NPs, Bi 2 - 2x Co x Cd x O 3 NPs, and Bi 2 - 2x Co x Cd x O 3 /rGO nanocomposites were 2.64 eV, 2.37 eV and 2.06eV respectively. The cyclic voltammetry technique was used to evaluate the functioning electrodes. In contrast to un-doped Bi 2 O 3 , the synergistic effects of Co, Cd, and r-GO on the substituted material increased the specific capacitance. The pure Bi 2 O 3 , doped Bi 2 - 2x Co x Cd x O 3, and Bi 2 - 2x Co x Cd x O 3 /rGO photocatalyst degraded 62 %, 85 %, and 95.4 % respectively of RB-5 dye after 105 min of sunlight. The phytotoxicity analysis examined the germination of Hordeum vulgare seeds in treated and untreated RB-5 dyes. Additionally, scavenging investigations using reactive species trapping to confirm the dominant reactive species were evaluated. Bi 2 - 2x Co x Cd x O 3 /rGO nanocomposites are better at photocatalysis and have a narrow bandgap, which makes them useful as solar-active photocatalysts for getting rid of dyes in wastewater. In future, their composites with conducting polymers may improve their electrochemical and photocatalytic behaviour as well. [ABSTRACT FROM AUTHOR]

Green hydrogen is a crucial element in the hydrogen value chain, encompassing hydrogen production, transportation, storage, and application. The production of green hydrogen via NaBH 4 hydrolysis (SBH) entails a high cost. However, the fast kinetics of this process with a catalyst compensate for the substantial cost, especially in specific applications, such as local or intermittent use. Silver is known for its excellent catalytic properties. Its high catalytic activity is a key factor in achieving efficient hydrogen generation from (SBH). In this study, a nanocomposite catalyst composed of silver nanoparticles (AgNPs), CoFe 2 O 4 , and carbon nanotubes (CNT) was investigated to demonstrate an effective catalyst design approach to achieve enhanced hydrogen generation performance. The H 2 production rate in the presence of Ag-based/CoFe 2 O 4 –CNT was 320 mL min−1 g−1, and the apparent activation energy was 14.7 kJ mol−1, superior to that of Ag-based catalysts reported in the literature. Analyses of the observed outcomes revealed that the CNT was decorated with well-dispersed AgNPs and CoFe 2 O 4 nanoparticles. The synergistic effects of AgNPs, CoFe 2 O 4 , and CNT were demonstrated by analyzing the kinetic behaviour of each component based on systematic comparisons. Furthermore, the paramagnetic property of CoFe 2 O 4 enables harvesting of the catalyst using an external magnetic field, and it was verified that the reactivity of the collected catalyst was maintained throughout seven successive cycles. The outstanding catalytic performance of Ag/CoFe 2 O 4 – CNT should be attributed to the uniform dispersion of nanoparticles on the CNT surface. Furthermore, our key approach for developing efficient Ag-based carbon advanced catalysts for SBH in the future is to ensure their suitability for industrial applications. Graphical illustration for the hydrogen production by hydrolysis process. [Display omitted] • A magnetic Ag/CoFe 2 O 4 -carbon nanotube nanocomposite was designed and synthesized. • Highly dispersed CoFe 2 O 4 and AgNPs are evenly embedded on the CNT. • Reaction kinetics followed during hydrogen production under different experimental conditions have been investigated. • The ACC catalyst demonstrated high activity, good recyclability, and low activation energy. [ABSTRACT FROM AUTHOR]

As a kind of ultra-high temperature ceramic, TaC is widely used in aerospace field. In order to improve its high temperature oxidation resistance, SiC is usually added as a second phase. TaC-SiC nanocomposites prepared by precursor-derived ceramic method have the advantages of low pyrolysis temperature, small particle size and uniform phase composition. Some studies have used solid polycarbosilane (PCS) as the precursor of SiC. However, it has problems such as high cost and need to add solvent. In this work, TaC-SiC nanocomposites were prepared by precursor-derived ceramic method with polytantaloxane (PTO) and vinyl-containing liquid polycarbosilane (LPVCS) instead of PCS as raw materials after 2 h pyrolysis at 1600 °C. The obtained TaC-SiC nanocomposites have a particle size of about 200 nm and a grain size of 15–40 nm, wrapped by 1–2 nm amorphous carbon shells, which is beneficial to inhibit grain growth. By analyzing the oxidation mechanism of TaC-SiC nanocomposites, it was found that higher SiC content was conducive to antioxidant, because the SiO 2 protective layer formed by oxidation insulated O 2 diffusion. [ABSTRACT FROM AUTHOR]

Zircon (ZrSiO 4) is an inexpensive and widely available material with excellent thermal properties that makes it an ideal candidate for thermal barrier coatings. Previous works have demonstrated the feasibility of obtaining coatings with a high retention of zircon by plasma spraying of ZrSiO 4 and ZrSiO 4 /ZrO 2 suspensions. Suspensions of ZrSiO 4 /Al 2 O 3 and ZrSiO 4 /TiO 2 were produced by dispersing a micrometric zircon powder into alumina and titania colloidal sols, optimising their colloidal stability and rheological behaviour. Optimised slurries were plasma sprayed onto metallic substrates, obtaining coatings with the typical morphologies obtained by suspension plasma spraying (SPS). Nanostructured coatings with nanoparticles embedded in the molten matrix were obtained at higher proportions of sprayed colloidal sol. The high retention of ZrSiO 4 in the final coatings and the formation of new crystallographic phases of mullite and zirconium titanate by reaction of the by-products of zircon decomposition (SiO 2 and ZrO 2) and the Al 2 O 3 and TiO 2 colloids was demonstrated. [ABSTRACT FROM AUTHOR]

The brittleness and limited plastic deformation of ceramics restrict their applications. In this work, the effects of pristine (CNT P), functionalized (CNT OH , CNT COOH) and silanized MWCNTs on the mechanical properties of Silicon Carbide obtained by pyrolyzing polycarbosilane SMP-10 were studied. Functionalization with 3-glycidoxypropyltrimethoxy was analyzed through dispersion stability, zeta potential, and EDS analyses, revealing increased silicon content and colloidal stability in silanized MWCNTs. However, silanized MWCNTs led to reduced mechanical properties in composites, while untreated MWCNTs (CNT P , CNT OH , CNT COOH), showed a substantial increase in modulus by 74.2 %, 86.9 %, and 30.5 %, respectively. The observed enhancement in mechanical properties exceeded the outcomes predicted by the rule of mixtures, suggesting notable morphological changes induced by MWCNTs. Potential underlying factors including toughening mechanisms and changes in porosity were evaluated and discussed in depth. Composites with untreated MWCNTs showed nearly a two-fold increase in fracture toughness. This work shows a streamlined approach for the development of ceramic nanocomposites (CNCs), achieving significant improvement in mechanical properties through pyrolysis, surpassing traditional methods reliant on densification processes. These findings demonstrate the substantial potential of CNCs, enhancing their suitability for advanced engineering applications. [ABSTRACT FROM AUTHOR]

It is a challenge to improve the long-term durability of Pd-based electrocatalysts for oxygen reduction reaction (ORR) in fuel cells. Herein, Pd/CeO2-C-T (T = 800 °C, 900 °C and 1000 °C) hybrid catalysts with metal–support interaction are prepared from Ce-based metal organic framework precursor. Abundant tiny CeO2 nanoclusters are produced to form nanorod structures with uniformly distributed carbon through a calcination process. Meanwhile, both carbon and CeO2 nanoclusters have good contact with the following deposited surfactant-free Pd nanoclusters. Benefited from the large specific surface area, good conductivity and structure integrity, Pd/CeO2-C-900 exhibits the best electrocatalytic ORR performance: onset potential of 0.968 V and half-wave potential of 0.857 V, outperforming those obtained on Pd/C counterpart. In addition, the half-wave potential only shifts 7 mV after 6000 cycles of accelerated durability testing, demonstrating robust durability. [ABSTRACT FROM AUTHOR]

Dielectric capacitors are commonly used in electronic and electric power systems due to their excellent charging and discharging rates and ultra-high power densities. Especially, with the rapid development of new energy vehicles industry, high-temperature films capacitors are urgently needed, while the conductivity loss of polymer capacitive films at high temperatures sharply increases, which should be significantly suppressed for achieving excellent energy storage performance. This paper presents a composite film with polyetherimide (PEI) as the matrix, and core-shell structured particle ceramic as fillers where high polarization of barium strontium titanate (BaSrTiO 3) as the core and excellent insulation strength of alumina (Al 2 O 3) as the shell, respectively, achieving a synergistic enhancement of breakdown strength and dielectric constant of Al 2 O 3 @BaSrTiO 3 /PEI composite film. More importantly, the Al 2 O 3 layer with moderate dielectric constant can effectively relieves the electric field distortion at the interfacial regions due to the large difference between BaSrTiO 3 fillers and PEI matrix. The composite film demonstrates exceptional thermal and cycling stability, as well as energy storage properties within the studied temperature range, a discharge energy density of 4.67 J/cm3 at 150 °C. The enhanced mechanism of energy storage performance is revealed bycomparatively analyzing of the microstructure and dielectric properties of BaSrTiO 3 /PEI, Al 2 O 3 /PEI, and Al 2 O 3 @BaSrTiO 3 /PEI composite films. This paper presents a modification strategy of inorganic/organic composite films by increasing both of dielectric constant and electric breakdown strength at elevated temperature. [ABSTRACT FROM AUTHOR]

Magnesium-doped zinc oxide thin films were dip-coated onto porous ceramic and glass substrates under identical conditions (50 layers, same doping ratio). Structural, morphological, and photocatalytic properties were characterized using X-ray diffraction (XRD), scanning electron microscopy (SEM), energy-dispersive X-ray spectroscopy (EDX), UV–visible spectrophotometry, and confocal microscopy. XRD analysis indicated a shift in peak positions towards higher angles, increased grain size, and lattice distortion on both substrates. Unique flower-shaped crystalline granulates were observed exclusively on the ceramic substrate (DD3Z). The energy gap decreased on the ceramic and increased on the glass substrate. The photocatalytic activity was evaluated using an aqueous orange II solution, showing significantly higher decomposition (80 ± 0.53 % after 6 h) on the ceramic compared to the glass substrate (30 %). The enhanced performance on ceramic substrates, particularly with DD3+ZrO 2 , was attributed to increased microporosity, surface roughness, and active material incorporation, facilitating greater photocatalytic efficiency. The findings suggest promising applications of these materials for efficient and cost-effective photocatalysis, with potential for reuse after thermal treatment at 500 °C. [ABSTRACT FROM AUTHOR]

This research is essential for the progress of nanocomposite technology, with ramifications for society. The development of economical and high-performing nanocomposites may result in improved and adaptable optoelectronic devices, therefore contributing to technical progress and economic advantages. The (PMMA-SiO2/CuO) nanocomposites(NCs) have been prepared using the solution cast method. This study examined the structural, optical, and electrical characteristics of nanocomposites consisting of PMMA-SiO2/CuO. The nanoparticles were uniformly distributed throughout the composite, resulting in a cohesive network within the polymer matrix, as evidenced by the optical microscope photos. The FTIR analysis showed a shift in the peak location and changes in the shape and intensity compared to the pure PMMA sample. The findings about the optical characteristics indicate a significant increase in absorption by approximately 331% (from 0.65 to 2.77) at a wavelength of 520 nm. The absorbance, refractive index, and optical conductivity of pure PMMA exhibited an increase with the rising concentration of (SiO2/CuO) nanoparticles. Additionally, the energy gap experienced a decrease of roughly 120% (from 4.01 to 1.81 eV) for allowed indirect transitions and 248% (from 3.48 to 1.05 eV) for forbidden indirect transitions with increasing concentration of (SiO2/CuO) nanoparticles. The nanocomposites of PMMA-SiO2/CuO exhibit a significant absorbance level in the ultraviolet (UV) region. As the frequency of the applied electric field increased, the dielectric constant and dielectric loss of the (PMMA-SiO2/CuO) nanocomposites decreased, as indicated by the experimental results. With an increase in frequency, the electrical conductivity of an alternating current (A.C.) increases. The dielectric loss of pure PMMA exhibited an increase with the increasing concentration of (PMMA-SiO2/CuO) nanoparticles. At a frequency of 100 Hz, the presence of SiO2/CuO nanoparticles in PMMA increased the dielectric constant by about 44% and the A.C. electrical conductivity by approximately 328% when the nanoparticles accounted for 6% of the total weight. The pressure sensor application investigation findings on NCs demonstrate a direct correlation between the applied pressure and the rise in electrical capacitance (Cp). [ABSTRACT FROM AUTHOR]

Generating a clean and sustainable hydrogen using the naturally available electrocatalysts to split water is among the primary energy resources adopted by the global industries. Transition metal dichalcogenides such as tungsten disulfide (WS 2) provide abundant active sites to foster hydrogen evolution reaction (HER). A simple hydrothermal process was employed to synthesize WO 3 ·H 2 O (hydrated tungsten trioxide) and WO 3 nanoparticles. The inclusion of WS 2 into the oxide has enhanced the ionic movement, which has improved the catalytic performance of the composite. The hydrophilic nature of WO 3 has facilitated the conversion of water molecules into adsorbed hydrogen, which was then spilled over the HER active sites of WS 2 to produce hydrogen. Thus, the WO 3 ·H 2 O/WS 2 catalyst achieved a current density of 10 mA cm−2 at an overpotential of 383 mV with Tafel slope of 77 mV dec−1 under neutral conditions and a hydrogen evolution rate of 0.33 mmol h−1 cm−2 at −0.5 V versus RHE. [Display omitted] • A tungsten-based composite, WO 3 ·H 2 O/WS 2 , was synthesized using a facile hydrothermal method at a relatively low temperature. • An overpotential of 383 mV at a current density of 10 mA cm−2 in HER is achieved under neutral conditions. • The estimated rate of hydrogen evolution is 0.33 mmol h−1 cm−2 at a potential of −0.5 V versus RHE. [ABSTRACT FROM AUTHOR]

The usage of non-renewable carbon-base fuel energy have created multiple issues such as global warming, environmental degradations etc. Replacing these non-renewable sources of energy with renewable energy (photocatalytic H 2 production) is a hot topic for researchers due to its sustainability and eco-friendliness. In this work MnO 2 , SnO 2 and their nanocomposites have been synthesized through simple hydrothermal and co-precipitation methods. The purpose of such nanocomposite fabrication is to synthesize a suitable heterostructure for maximum solar energy harvesting in water splitting. All the prepared samples of pure MnO 2 , SnO 2, and nanocomposites have been characterized through various techniques, which confirm the structure, functional groups, absorbance, morphology, elemental compositions, chemical compositions, and increase in photo-induced current as well as the photostability of such nanocomposites. The highest apparent quantum yield of the optimized MnO 2 @SnO 2 (first time reported as photocatalyst for H 2 production) were 21.7% at wavelength 420 nm, which is the highest ever reported for such (MnO 2 @SnO 2) nanocomposite. The enhanced photocatalytic behavior for H 2 production has been observed which is 3.67 times greater than pristine MnO 2. Such an enhancement is due to the synergistic effect of SnO 2 NPs decorated on the NTs of MnO 2. The present work provides a novel approach to produce hydrogen with high performance as efficient solar harvesting. • High-quality crystalline nanocomposites of MnO 2 @SnO 2 have been synthesized. • Various characterizations have been performed like XRD, FTIR, EDX, SEM, XPS, TEM, HR-TEM, EIS and GCG spectroscopies. • The suitable bandgap (MS-30) sample shows visible light absorption. • MS-30 nanocomposite shows an enhanced photocatalytic H 2 production performance. [ABSTRACT FROM AUTHOR]

Si/graphene nanocomposite is regarded as an advanced lithium-ion anode material, attributable to its advantageous microstructure and exceptionally high theoretical specific capacity. This study demonstrates a novel approach for the preparation of Si/graphene nanocomposites, achieved through the pulsed discharge method employing graphite and Si strips as precursors. We devised two distinct "one-step" synthetic routes through pulsed discharge of different wire arrangements. The characterization results of the obtained samples unveiled the presence of Si/graphene composite and Si@carbon layer composite. In addition, the formation mechanisms of Si/graphene nanocomposites have been proposed, different wire arrangements lead to the different energy deposition processes, inducing different robust mechanical and thermal effects on the products. The formed Si clusters either deposit on the surface of exfoliated graphene or become encapsulated within curling graphitic layers, forming a core@shell structure. This work not only presents a straightforward and innovative approach for synthesizing Si/graphene nanocomposites but also contributes valuable insights into the underlying mechanisms governing their formation. [ABSTRACT FROM AUTHOR]

Plastic waste and wastewater are indeed significant environmental issues that have wide‐ranging impacts on ecosystems, human health, and the economy. This study outlines the synthesis of biodegradable polyvinyl alcohol (PVA)–starch polymeric films incorporating multiwalled carbon nanotubes (MWCNTs) derived from plastic waste and unzipped carbon nanotubes oxides (UMCNOs) as co‐filled nanomaterials. These films were formulated based on data generated using a mixture design method in Design Expert 13 software, resulting in the synthesis of 19 films utilizing five types of PVA–starch polymer solutions (Types A–E). The synthesized films underwent characterization to study their surface morphology via scanning electron microscope and Fourier transform infrared spectroscopy analysis. Subsequently, the films were individually subjected to vacuum filtration, through which cationic dyes such as methylene blue (MB) and anionic dye Congo red (CR) were passed in batches. The highest removal efficiency of 96.43% for MB dye was achieved, accompanied by an exceptionally high flux of 3146.78 LMH. Similarly, the maximum removal of 88.08% for CR was observed with a flux of 1512.66 LMH. The renewable active sites mechanism resulted in increased dye removal with every cycle. Results indicated efficient reusability, particularly when washed with ethanol–water solution. [ABSTRACT FROM AUTHOR]

Composite sandwich structures, which are widely employed in engineering structures, require a multitude of inserts. In certain instances, the necessity for a specialized insert arises from the unique characteristics of a particular application. In applications such as weather radar radomes, double-curved sandwich panels should be designed with electromagnetic (EM) transparency as a primary objective. The use of metal inserts should be restricted to the absolute minimum. Given the limitations of using metal materials to protect against EM radiation and the need to enhance the load-bearing capacity of the joint against pull-out loads, a composite insert has developed as an innovative solution. In this study, a composite insert of a double-curved sandwich dome has been developed using silica nanoparticles, and its mechanical strength against pull-out load has been evaluated through both experimental and numerical analysis. The strength results obtained have been compared with analytical estimates. Additionally, the buckling of the double-curved sandwich dome against a wind speed of 220 km/h has been investigated numerically. The critical buckling load for wind loading for the full-scale sandwich radome was estimated to be 16,303 N. According to the numerical results obtained with the Abaqus finite element (FE) software, the maximum pull-out force applied to the connection area is approximately 10.7 kN. A parametric study of geometric variables and experimental results showed that it is possible to achieve a stronger composite insert (by 1 wt % nano silica particles) by 20.7% lighter and 102.65% more bearing capacity. [ABSTRACT FROM AUTHOR]

This work is an attempt to evaluate the effect of multi-wall carbon nanotube (MWCNT) reinforcement on the properties of non-crimp fabric (NCF) carbon fiber-reinforced polymer hybrid composite (CFRP). MWCNT NCF-CFRP plates were produced by vacuum infusion. Epoxy-MWCNT mixtures were prepared by adding a surfactant, Triton-X 100, and ethanol and mixing ultrasonically. The plates were subjected to thermal and electrical conductivity, DSC and FT-IR characterizations, and tensile testing. SEM image analyses evaluated tensile fracture surfaces. Results showed that 0.5 wt% MWCNT-reinforced nanocomposite samples exhibited better tensile properties than pure NCF-CFRP composites and other nanocomposite samples. The 1.5% MWCNT reinforced sample was the best conductor at all temperatures. The temperature increases also increase the conductivity. However, the conductivity value of 0.5% MWCNT reinforced material increased significantly at low frequencies such as 100–10,000 Hz. The heat reaction of the 0.5 wt% MWCNT nanocomposite was also a bit higher than that of 1–1.5 % wt MWCNT nanocomposites, indicating a decrease in the cure. [ABSTRACT FROM AUTHOR]

We presents an innovative approach to addressing the mechanical properties limitations of fluororubber (FKM) in the industrial field. A novel functionalized nano-silica spheres (SiO2), grafted with amino groups, were constructed by utilizing chemical grafting. The surface modification of the nanosilica microspheres enables the formation of C=N bonds between the amino-functionalized nanosilica microspheres and FKM promoting high dispersion and strong interfacial bonding of SiO2, resulting in an exceptional mechanical enhancement function for FKM composite. Compared to original FKM, the FKM/SM-A-10 composite demonstrates remarkable improvements in both tensile strength and hardness by 242% and 49%, respectively. Additionally, there is a notable 40% enhancement in thermal conductivity of the FKM/SM-A-10 composite. This straightforward and efficient manufacturing approach for achieving high-performance FKM proves to be a valuable and practical foundation for industrial design. [ABSTRACT FROM AUTHOR]

The availability of fresh water is limited compared to its huge consumption. Conversely, certain industries like dyes, textiles, paper, and tanning not only consume vast quantities of fresh water, but also generate significant amounts of wastewater that poses severe threats to living organisms. The present investigation focuses on the degradation of Rhodamine-B (Rh–B) as a model pollutant by using the nanocomposite based on waste scrap tire-derived activated carbon (AC) and titanium dioxide (TiO 2). These nanostructures were fabricated using wet chemistry techniques. Analysis using scanning electron microscopy (SEM) revealed that the morphology of the structures remained largely unchanged even with a concentration of 6 mg of AC. X-ray diffraction (XRD) results confirmed the successful fabrication of rutile and anatase phases of TiO 2 @AC nanocomposite. The XPS results confirmed the presence of AC and TiO 2 in the composite. Furthermore, the optical band gap of the nanocomposites decreased up to 17.17 % and 34.57 % through direct and indirect methods respectively, owing to the varying quantity of AC used. The narrowing of optical band gap and the increased surface oxygen vacancies were caused by the successive addition of AC during the synthesis of nanocomposites. This resulted in the efficient degradation of Rhodamine-B (Rh–B) using adsorption and photocatalytic oxidation. The findings demonstrate a significant influence of AC on the TiO 2 catalyst in the removal of Rh–B dye. The maximum efficiency of dye removal, reaching up to 99.14 %, was achieved with the highest concentration of AC, thus demonstrating almost complete elimination of Rh–B dye. The findings suggest that the use of waste scrap tires can be effectively applied to design efficient photocatalysts for addressing the wastewater management issues. [ABSTRACT FROM AUTHOR]

There is a growing threat of wastewater pollution impacting human access to clean water. The surge in pharmaceuticals and personal care products (PPCPs) in such water has reached alarming levels, posing an unprecedented threat to aquatic ecosystems and human health. Conventional wastewater treatment is not specifically tailored to address the presence of PPCPs. This paper examines the possibility of using nano-chitin and chitosan as effective and sustainable adsorbents for the removal of PPCPs from wastewater. The recent progress in functionalized nano-chitin or chitosan composites is reviewed with attention to enhanced adsorption capacity and selectivity toward different classes of PPCPs. Unique features of nano-chitin and chitosan, such as their large surface areas and biocompatibility making them a good choice for PPCP adsorption, are also discussed. Critical evaluation is given about how these nanomaterials absorb PPCPs by looking at various mechanisms like electrostatic interactions, hydrogen bonding, hydrophobic interaction, among others. Finally, future research directions provided for improving performance and scalability of such bio-based adsorbents are discussed. [ABSTRACT FROM AUTHOR]

In the present work, the development of nanocomposites was carried out by processing the nanofillers viscogel clay B8 and vanadium oxide with the polycaprolactone (PCL) matrix, through a twin-screw extruder. The evaluation of the nanomaterial obtained by X-ray diffraction technique showed that the addition of nanoparticles caused change in the crystallization process and in the crystallinity index, due to the action of them as a nucleating agent. Evaluation of thermogravimetric analysis, it was observed an increase in the thermal stability of nanocomposites containing clay. Analyzing the SEM micrographs, it was observed that there was a good dispersion and distribution of nanofillers in the matrix. The differential scanning calorimetry and X-ray diffraction technique, showed the possibility of nanoparticles are acting as a nucleating agent, in some mixtures there was change in the values of crystallinity index. Through nuclear magnetic resonance analysis, it was evaluated a good homogeneity of the nanofiller in the matrix due to the intermolecular interaction promoting a better dispersion and distribution of the nanoparticle in the polymer. [ABSTRACT FROM AUTHOR]

Water pollution due to organic compounds has emerged as a global concern. Among various methods for wastewater treatment like advanced oxidation process, photodegradation, reverse osmosis, etc., adsorption is an economical and effective method. Different research scientists have focused on developing low-cost materials for the adsorption of organic pollutants from aqueous streams. The Discovery of M-xenes has led to a new and interesting vein of research. This article summarises M-xenes and M-xenes based nanocomposites for wastewater treatment. Adsorption kinetics and mechanism is also discussed in this paper. The adsorption is due to chemical attractions between pollutants and functional groups on the surface of M-xenes. Surface modified M-xenes have the potential to be excellent adsorbent materials for water remediation. Various factors affecting the adsorption capacity of M-xenes are discussed. Lastly, the future prospects for developing M-xenes as efficient, low-cost and non-toxic materials for water remediation are also addressed. [ABSTRACT FROM AUTHOR]

A zinc oxide/carbon nanotube hybrid (ZnO/MWCNT) was synthesized utilizing a straightforward precipitation technique based on the physical approach of pulsed laser ablation. Various techniques were employed to investigate the composition, morphology and optical of the synthesized nanocomposite. The techniques employed were X-ray diffraction, Raman spectroscopy, transmission electron microscopy, FT-IR and thermal gravimetric analysis (TGA) to confirm the compete decoration to be applicable for removal Ni(II) ions in an aqueous solution. ZnO have a hexagonal wurtzite structure connected to hexagonal graphite of MWCNT from XRD. The interaction between ZnO and CNTs resulted in a reduction in the domain of sp2 bonds, according to Raman. From TGA, we can attribute the reduction in thermal analysis to the oxidation of surface hydroxyl functional groups (-OH), the evaporation of surface solvent and the presence of ZnO's inorganic oxide structure compared to pristine MWCNT. These findings confirmed that adding ZnO NPs to MWCNT caused more structural flaws and surface disorder, even though the structure of the CNTs stayed the same. We then investigated numerous factors affecting the extraction of Ni(II) ions, including pH, duration of extraction, amount of nanosorbent used and circumstances. We observed the optimal conditions at room temperature, pH of 5.9, nanoadsorbent dosage of 0.2 g/L and contact time of 1 h. Atomic absorption spectrometry easily monitored the kinetics of this reaction. The Langmuir, Freundlich and Redlich–Peterson isotherm models explain the mechanism underlying the adsorption equilibrium isotherm. Furthermore, regeneration experiments revealed that the adsorbent still maintained a high adsorption capacity after six cycles, demonstrating remarkable potential for use in environmentally friendly applications. [ABSTRACT FROM AUTHOR]

Pressure sensors based on advanced materials have gained high attention for their potential applications in various fields, including sports training. This study focuses on the development of poly(vinylidene fluoride-trifluoroethylene) (P(VDF-TrFE))/graphene composite films as high-performance pressure sensors. The composite films were fabricated using a casting method, and their morphological, structural, thermal, mechanical, and electrical properties were comprehensively characterized. The incorporation of graphene nanoplatelets (GnPs) into the P(VDF-TrFE) matrix led to the formation of a percolated conductive network, resulting in enhanced electrical conductivity and pressure sensitivity. The composite film containing 5 wt% GnP exhibited remarkable sensing capabilities, boasting an elevated sensitivity of 0.85 kPa−1, a rapid response time of 50 ms, and exceptional resilience over 1000 loading-unloading cycles. Moreover, the incorporation of GnP substantially augmented the mechanical properties, with a 65 % enhancement in tensile strength and a 92 % surge in Young's modulus when juxtaposed against pristine P(VDF-TrFE) films. The superior property of these P(VDF-TrFE)/graphene composite pressure sensors, along with their excellent mechanical properties, make them promising candidates for sports training applications, enabling the monitoring and analysis of various biomechanical parameters to optimize athletic performance and prevent injuries. [ABSTRACT FROM AUTHOR]

In response to the escalating need for nanomaterials characterized by enhanced properties and reduced environmental impact, this study addresses critical challenges associated with conventional nanomaterial synthesis methods, particularly focusing on concerns related to environmental toxicity and economic feasibility. In this study, we report the eco-friendly synthesis of silver-zinc oxide nanocomposites using leaf extracts of Quassia indica (QI- Ag: ZnO NC). The synthesized QI- Ag: ZnO nanocomposites were characterized using various techniques including UV-visible spectroscopy, X-ray diffraction (XRD), Fourier-Transform Infrared Spectroscopy (FTIR), Dynamic Light Scattering (DLS), Field-Emission Scanning Electron Microscopy (FE-SEM) with Energy Dispersive X-ray Spectroscopy (EDX), High Resolution Transmission Electron Microscopy (HR-TEM), and Selected Area Electron Diffraction (SAED). The photocatalytic activity of the biosynthesized QI- Ag: ZnO NC was evaluated against several textile dyes. Reactive Blue-220 exhibited the highest percentage of degradation (99.97%), closely followed by Reactive Blue-222 (99.37%), while Reactive Red-120 displayed significant degradation (94.62%). Remarkably, these nanocomposites exhibited significant photocatalytic degradation of the tested dyes, suggesting their potential application in wastewater treatment for dye removal. Furthermore, phytotoxicity studies were conducted to assess the impact of the nanocomposites on plant growth and brine shrimp mortality. To evaluate their cytotoxicity, the nanocomposites synthesized were assessed using the MTT assay on MCF-7 and MDA-MB-231 cancer cells. These findings suggest that QI- Ag: ZnO NCs have promising applications in environmental remediation and cancer therapy, opening avenues for further advancements in the arena of nanomaterial synthesis and utilization. [ABSTRACT FROM AUTHOR]

Since the advent of nanotechnology, nanocomposites (NCs) have been synthesized via novel approaches. In this regard, polymer-based NCs have been widely explored due to their exceptional characteristics as a result of the incorporation of nanofillers into the polymer matrix. In the present research, the synthesis of titanium oxide (TiO2) nanoparticles (NPs) was synthesized using Azadirachta indica seed extract. Polyvinyl alcohol (PVA) was used to synthesize metal oxide NCs. Using the solution casting approach, PVA/TiO2 NC films with various weight percentages of TiO2 NPs (2, 4, 6, and 8%) were fabricated. X-ray diffraction spectroscopy, field emission scanning electron microscopy (FE-SEM), ultraviolet–visible spectroscopy, and Fourier-transform infrared spectroscopy were employed to characterize the TiO2 and PVA/TiO2 NCs. The antibacterial activity of the TiO2 NPs and PVA/TiO2 NCs was investigated against Gram-positive (Staphylococcus aureus and Enterococcus faecalis) and Gram-negative (Proteus mirabilis and Pseudomonas aeruginosa) bacteria. Methyl orange and methylene blue breakdown of undoped TiO2 and PVA/TiO2 nanomixture was examined under UV–visible irradiation. Uniformly dispersed nanoflake particles were visible in the PVA film matrix and on the 4% TiO2 NC surface. X-ray diffraction analysis showed that TiO2 NPs synthesized using a higher concentration of the extract showed larger crystallite sizes, whereas those fabricated using a lower concentration of plant extract showed larger crystallite sizes. Among the different concentrations investigated, 4% PVA/TiO2 NCs showed the highest extent of degradation of methylene blue and methyl orange. Furthermore, these NCs showed the highest antibacterial activity. [ABSTRACT FROM AUTHOR]

we successfully developed a new class of nitrogen-doped carbon dots (N-CDs) using a unique combination of hyaluronic acid (HA), citric acid (CA), and urea. This synthesis, achieved through an efficient one-pot hydrothermal process, has ushered in a new era for bio-imaging and forensic science applications. The N-CDs, characterized techniques such as Transmission Electron Microscopy (TEM), X-ray Photoelectron Spectroscopy (XPS), and Photoluminescence Spectroscopy (PL), demonstrated outstanding fluorescence properties. These properties were maintained under various pH levels and even under prolonged UV exposure, showcasing their remarkable stability. The transformative potential of these N-CDs was further evidenced in their biocompatibility and efficacy in bio-imaging. When tested in vitro with human cell lines, the N-CDs not only exhibited efficient cellular uptake but also ensured minimal cytotoxicity, marking a significant advancement in safe and effective bio-imaging techniques. Moreover, in the realm of forensic science, the N-CDs proved to be a game-changer for latent fingerprint analysis. Their application on glass surfaces revealed minute fingerprint details, such as ridges and sweat pores, with unprecedented clarity. This exceptional performance is attributed to their luminous properties and their interaction with amino acids and proteins present in fingerprint residues. Our findings pave the way for these N-CDs, synthesized from HA, CA, and urea, to be recognized as versatile and powerful tools. They hold immense promise not only in advancing bio-imaging methodologies but also in revolutionizing forensic techniques for latent fingerprint detection across various surfaces. This study, therefore, presents a significant leap forward in both biomedical and forensic science fields, demonstrating the far-reaching applications of these innovative nanocomposites. [ABSTRACT FROM AUTHOR]

Semiconductor photocatalysts with engineered heterostructure are gaining attention for environmental remediations. The combination of two or more metal oxides with support materials has proved an effective strategy for better charge separation to lead to redox reactions. Therefore, the novel combination of tungsten oxide (WO3) and bismuth oxide (Bi2O3) with graphene oxide (GO) was studied to degrade methylene blue dye as a model organic pollutant. The novel composite material was synthesized using a facile hydrothermal route. The photocatalysts (i.e., WO3, WO3/Bi2O3, and GO/WO3/Bi2O3 composite) were characterized in terms of surface morphology by scanning electron microscope, elemental mapping by energy-dispersive X-ray, crystalline structure by X-ray diffraction, and functional group identification by Fourier transform infrared spectroscopy. The characterization analysis confirms the successful synthesis of all pristine and composite materials. The optical response of photocatalysts (WO3/Bi2O3) and composites photocatalyst (GO/WO3/Bi2O3) was checked by UV–visible spectroscopy using the Tauc plot method. The considerable reduction in energy bandgap from 2.9 (for WO3/Bi2O3) to 2.2 (for GO/WO3/Bi2O3) suggests that the proposed composite material is not only effective under natural sunlight but also a potential material with improved charge separation. The optimization of influencing parameters was done, and the best degradation efficiency of about 98% was achieved under pH = 9, composite dose = 30 mg per 100 mL, and H2O2 concentration = 13 mM, with the reaction time of 180 min under ambient sunlight. Kinetic studies confirmed that the photocatalytic degradation process followed the 1st-order kinetic model. The response surface methodology (RSM) was employed to analyze the data statistically. [ABSTRACT FROM AUTHOR]

Nano-size spinel ferrite CoFe2O4 (CFO), ferroelectric BaTiO3 (BTO), and their nanocomposites BTO@CFO (BTO nanoparticles are added during the synthesis of CFO) and CFO@BTO (CFO nanoparticles are added during the synthesis of BTO) were synthesized using a combination of chemical co-precipitation and sol–gel routes, respectively. The phase formation and crystallinity of the bare CFO and BTO and their nanocomposites were verified via x-ray diffraction (XRD) patterns. High-resolution transmission electron microscopy (HRTEM) revealed the formation of the nanocomposites. Magnetization measurements confirmed the ferromagnetic behavior of all the samples except BTO, in which superposition of a weak ferromagnetic and diamagnetic response occurred due to its nanostructure. Magnetization versus temperature (M–T plot) measurements showed an anomaly near the ferroelectric-to-paraelectric phase transition of BTO. Also, the dielectric constant (ε′) and loss tangent (tanδ) with respect to frequency (102–106 Hz) and temperature (300–700 K) were examined. The ε′–T curve of the nanocomposites exhibited an anomaly at the same temperature as observed in the M–T plot, indicating the inherent magnetoelectric coupling in the nanocomposites. The energy storage properties of BTO and the nanocomposites were examined via P–E loop analysis and confirmed that the CFO@BTO sample exhibits maximum energy storage efficiency. [ABSTRACT FROM AUTHOR]

Electronic devices and communication systems are highly susceptible to interference from unwanted electromagnetic waves. High-performance electromagnetic interference (EMI) shielding offers a solution to this issue. In this work, we discuss the design of an EMI shielding material composite using natural rubber (NR) filled with polyaniline (PANI), multi-walled carbon nanotubes (MWCNT), and ferric oxide (Fe2O3). Different properties of the material composite are studied using scanning electron microscopy (SEM), X-ray diffraction (XRD), and Fourier transform infrared (FTIR) spectroscopy. We tested the EMI shielding efficiency of the developed material in the X band and the Ku band. The measurements revealed improved shielding effectiveness when compared to similar microwave shielding materials. In terms of flexibility and cost-effectiveness, this novel composite also proved to be a better alternative. [ABSTRACT FROM AUTHOR]

The study revealed a correlation between the cytotoxicity and antioxidant activity of iron oxide nanopowders produced by the radiation-chemical method and the choice of precursors (iron (III) nitrate or iron(II) sulfate), and the temperature of pre-annealing of the synthesized product, and also irradiation with accelerated electrons. Notably, high and lowabnormal cytotoxicity of aqueous suspensions of samples S300 and S400, respectively, annealed at temperatures of 300 and 400 °C, was observed for the first time at all concentrations (0.1–1.0 ml/mg). The likely cause of this abnormal cytotoxicity was identified as alterations in the textural and structural properties of NP after annealing.Furthermore, a significant impact of electron beam irradiation on the antibacterial and antioxidant properties of both unannealed and annealed iron oxide NP was discovered with irradiated samples exhibited lower cytotoxicity compared to non-irradiated ones. Additionally, the deposition of nanosilver on the surface of iron oxide powders was found to significantly influence their biological properties, with the survival of Vero cell cultures being dependent on the composite concentration in the aqueous suspension. A study of the oxidative stress of composites based on iron oxides coated with silver showed that they significantly increased cell viability, and at a concentration of 1 mg/ml provided complete mitigation of oxidative stress in cells. • The cytotoxicity of iron oxide nanopowders is dependent on electron irradiation. • The sample of iron oxide annealed at 400 °C showed an unusually high level of cytotoxicity. • Cytotoxicity of iron oxide nanopowders may depend on silver coating. • Silver coating on iron oxide has a compensatory effect on oxidative stress in cells. [ABSTRACT FROM AUTHOR]

The green method provides stable, rapid, and eco-friendly methods for synthesis nanoparticles with plant extract as capping and reducing agents. This method renders biocompatibility, scalability, and potential medical applications of nanoparticles. This study green synthesized CuO/TiO 2 and ZnO/TiO 2 nanocomposites using Parkia timoriana bark extract. The synthesized nanocomposites were determined utilizing UV–vis DRS FTIR, XRD, TGA, AFM, FE-SEM, E -DAX, HR-TEM, and XPS. Antioxidant assay and antidiabetic studies revealed the biological activity of nanocomposites. The antioxidant property in ZnO/TiO 2 (84.07 %) was higher than in CuO/TiO 2 nanocomposites (72.76 %). The IC 50 value of CuO/TiO 2 and ZnO/TiO 2 in α-amylase inhibition assay was 72.12 μg/mL and 75.95 μg/mL, respectively and IC 50 value of CuO/TiO 2 and ZnO/TiO 2 in α-glucosidase inhibition assay was 30.80 μg/ml and 25.69 μg/ml. Thus, it concludes ZnO/TiO 2 nanocomposites exhibited higher antioxidant and antidiabetic activity than CuO/TiO 2 nanocomposites. These results show that biosynthesized nanocomposites can be used for treating diseases. [ABSTRACT FROM AUTHOR]

This work describes the development and characterization of tetragonal barium titanate nanoparticles (BTO NPs) and their surface functionalization with dopamine dodecylamine (DDA), a lipophilic organic ligand. The so‐obtained lipophilic NPs (BTO‐DDA) are then formulated at low loadings (< 5 wt.%) into liquid photocurable resins for vat photopolymerization (VP) and 3D printed into solid objects. The printed composites are mechanically characterized in order to assess the effect of the nanomaterial on the mechanical properties of the 3D printed polymer, revealing no significant variations in the mechanical properties (tensile or flexural) of the nanocomposites compared to the original polymer matrix. In light of these results, the printed nanocomposites are studied in terms of their capacity to generate a separation of charge by the piezoelectric effect, typical of the BTO crystal structure. This study reveals that BTO‐loaded nanocomposites display outstanding piezoelectric coefficients as high as 50 pC/N when BTO‐DDA is formulated at 3.0 wt.%, only slightly less than one‐third of the piezoelectric coefficient previously reported for bulk BTO, while preserving the mechanical properties of the polymer matrix. [ABSTRACT FROM AUTHOR]

In order to improve the low specific surface area and high recombinant light generation carriers of BiOBr, loading BiOBr onto suitable Metal Organic Frameworks (MOFs) is an effective strategy to unleash its efficient visible light response and intrinsic catalytic activity. In this study, using classic MOF CAU‐17 as a precursor, using a straightforward co‐precipitation technique, four BiOBr/CAU‐17 composites with distinct MOF contents values BCAU‐1, BCAU‐2, BC, AU‐3, and BCAU‐4 were created, and their photo‐catalytic characteristics were examined. The BCAU‐2 composite exhibited much higher photo‐catalytic degradation efficiency for Rhodamine B (RhB) and Tetracycline (TC) than the pristine materials, counter compositions, and early reported materials. XRD, SEM, TEM, XPS, and EDX results revealed the strong synergistic photo‐catalytic effect of BiOBr and CAU‐17. The photocatalytic degradation of TC was significantly enhanced by the BiOBr bimetal modification, with the 2 wt.% BiOBr/CAU‐17 nanocomposite achieving an 87.2 % degradation of TC and 82 % Total Organic Carbon (TOC) removal within 60 min. The high photo‐degradation efficiency of BCAU‐2 composite should be attributed to the efficient transfer of photo‐generated carriers at interfaces and the synergistic effect between BiOBr/CAU‐17. Furthermore, the experiments on the capture of the active species proved that the main active free radicals involved in the degradation of RhB and TC are attributed to the photo‐induced holes h+ and ⋅ O2− under visible light. The catalyst's efficacy is corroborated by the outcomes of photoluminescence spectroscopy and photo current response. This study offers a new understanding for the design of green synthesis schemes for photo‐catalytic dye degradation and removal of certain antibiotics from the aquatic environment. [ABSTRACT FROM AUTHOR]

Halloysite nanotubes (HNTs) have attracted considerable attention due to their unique properties and wide range of applications. This review explores HNT‐based nanocomposites, focusing on their preparation methods and improvements in mechanical, thermal, and barrier properties. Various synthesis techniques, including solution mixing, melt compounding, in situ polymerization, and surface modification, are discussed, along with their benefits and limitations. The role of HNT characteristics such as aspect ratio, dispersion, and surface chemistry in enhancing nanocomposite properties is examined. HNTs significantly boost mechanical properties, including tensile strength, Young’s modulus, and toughness, due to their reinforcement effects. Improved dispersion and interfacial adhesion between HNTs and the polymer matrix enhance these properties. HNTs also act as thermal barriers, improving heat resistance and dimensional stability, while enhancing barrier properties against gases and moisture. These synergistic effects allow for the customization of nanocomposites for specific applications in packaging, automotive, electronics, and biomedical fields. Future research should focus on optimizing synthesis methods and processing techniques to further improve HNT‐based nanocomposites’ performance. This review provides a comprehensive overview of HNT‐based nanocomposites, offering valuable insights for advancing nanomaterials science and engineering. [ABSTRACT FROM AUTHOR]

The preparation of polyimide matrix composites with low curing temperature and high mechanical properties is of great importance. In this study, a low‐cost and multi‐functional nanofiller, 5‐aminobenzimidazole grafted graphene oxide (5‐ABZ@GO) has been designed. By nucleophilic attack on 5‐aminobenzimidazole basic groups and doping of GO, the above requirements of polyimide composites were skillfully realized. The results show that when the addition of 5‐ABZ@GO is 1%, the 5‐ABZ@GO/PI nanocomposites can achieve complete imidized at 200°C. Moreover, the nanocomposite prepared by imidization at 200°C has good mechanical and thermal properties (tensile strength is 141.64 MPa, modulus is 6.05 GPa, T5% is as high as 543.5°C), which is better than the PI composites prepared at 320°C. This study provides an innovative approach to preparing polyimide composites that meet mechanical performance requirements while utilizing comparatively lower curing temperatures, low curing temperature polyimide resins provide a new path for integrated composites with structure–function integration. [ABSTRACT FROM AUTHOR]

Bio‐based flexible dielectric substrates have gained tremendous attention for their potential to reduce environmental risks from nonbiodegradable electronic waste. The present study demonstrates the fabrication of facile, nontoxic, and biodegradable chitosan‐based flexible dielectric substrate using graphene nanoplatelet (GNP) as a nanofiller. The detailed impact of different concentrations of GNP (1, 2, and 3 wt%) into the chitosan (CS) matrix was studied on physicochemical, morphological, mechanical, electrical, and thermal properties. The fabricated CS/GNP composites showed improved mechanical strength, thermal stability, and electrical properties compared with unmodified CS film. The composites exhibited excellent thermal stability (200°C) with a promising biodegradation rate (within 6 days). The mechanical strength of the unmodified CS film was increased unequivocally with 2 wt% GNP loading with tensile strength of 23.56 Mpa. Furthermore, the current–voltage (I–V) characteristic curves for CS/GNP (2%) and CS/GNP (3%) showed similar current conduction and ohmic behavior in flat, bending, and flat‐after‐bending modes. The dielectric measurements revealed that the CS/GNP composite with 2 wt% filler exhibited optimal performance having permittivity (έ) of 32.71 (at 102 Hz) with low dielectric loss of 0.04 (at 106 Hz). These results suggest that the dielectric films offer strong prospects as an eco‐friendly alternative for various applications. Highlights: Biodegradable chitosan‐based flexible dielectric films were prepared.Films were made using a simple solvent casting method with 1–3 wt% GNP filler.Optimum physicochemical and electrical properties were seen at 2 wt% GNP.CS/GNP (2%) film exhibited ohmic behavior in both flat and bending modes.Excellent dielectric properties were achieved at 2 wt% GNP filler. [ABSTRACT FROM AUTHOR]

High‐density polyethylene (HDPE) nanocomposites containing different optimized fractions of carbon nanofiber (CNF) at 6 wt.%, polyethylene glycol (PEG) at 4 wt.%, and copper oxide (CuO) nanorods in concentration ranges of 0.15, 0.5, and 2 wt.% were successfully melt processed using corotating twin extrusion and compression molding technique. The effect of PEG and CuO nanofiller on the HDPE matrix were studied, particularly for the percolation threshold for electrical conductivity, structural morphology, and other properties including thermal stability, thermal conductivity (TC), dielectric, and UV protection properties. It is observed that PEG acts as a good compatibilizer, facilitating better interfacial connection between CNF and HDPE matrix. The optimized composite with 0.15 wt.% CuO nanorods (H/C6/P4/Cu0.15) shows a fine morphology and strong interfacial connections between fillers and the matrix, as observed in FE‐SEM micrographs. This optimized composite exhibits improved thermal stability, higher thermal conductivity (0.0404 W.K−1.m−1), increased dielectric constant, reduced electrical volume resistivity (from 2.1 × 1015 to 2.1 × 106 Ω.cm), and lower optical band gap value (2.74 eV). Additionally, all prepared nanocomposites offer approximately 100% Ultraviolet Protection Factor (UPF) rating for UV protection. Highlights: The transformation of insulating HDPE into conducting HDPE composites.The effect of CuO nanorods was investigated in compatibilized HDPE composites.A percolation is achieved in the HDPE composite at 0.15 wt.% of CuO nanorods.PEG and CuO nanorods improved the multifunctional properties of the composite. [ABSTRACT FROM AUTHOR]

The interface between the polymer matrix and inorganic fillers plays a determinative role in dielectric properties of the composites. In this work, dielectric composites containing core‐shell structured BaTiO3@Al2O3 (BT@AO) nanoparticles and cyano functionalized cellulose (cyanoethyl cellulose, CEC) were prepared to achieve enhanced interface and dielectric properties. With the wide bandgap Al2O3 (AO) shell, the carrier motion inspired by elevating electric filed and temperature was significantly impeded in the composites. Meanwhile, the moderate dielectric constant and surface energy of AO shell between CEC and BaTiO3 (BT) alleviated the inhomogeneous local electric field distribution and improve the interfacial compatibility between inorganic filler and CEC matrix. As a result, enhanced dielectric properties including restrained dielectric loss (0.23 for BT@AO/CEC versus 0.51 for BT/CEC at 100 Hz), suppressed conductivity, increased breakdown strength and improved dielectric constant were accessed in the BT@AO/CEC composites. The excellent thermal conductivity of AO also offered the composites with additional advantage of low electrical conductivity at high temperature of 100°C (1.56 × 10−10 S/cm) exhibiting two orders of magnitude smaller than that of pure CEC. Highlights: Core‐shell structured BaTiO3@Al2O3 were prepared and incorporated into cyanoethylated cellulose to yield flexible nanocomposites.Carrier motion was significantly restricted by the wide band gap of Al2O3 shell.Enhanced interfacial compatibility was accessed in the BaTiO3@Al2O3/CEC composite.Improved dielectric properties and thermal conductivity were achieved. [ABSTRACT FROM AUTHOR]

Boron nitride (hBN) serves as an outstanding high‐performance polymer organic filler. However, its hexagonal crystal structure renders it chemically inert, thus limiting its applications. This study proposes the modification of hBN using economical amine and anhydride curing agents to reduce aggregation and enhance the heat conduction of epoxy resin. Specifically, the DETA curing agent and methyl tetrahydrophthalic anhydride (MTHPA) curing agent were grafted onto the hBN surface via ball milling and eco‐friendly water scrubbing processes. Subsequently, the modified functionalized BNNS were uniformly dispersed in epoxy resin via a wet process to form composite materials. Results indicate that both modified fillers maintain good dispersion at the epoxy interface. Compared to epoxy resin, the heat conduction of the EP/MTHPA‐BNNS composite material with 10 vol% loading increased by 212%. The EP/DETA‐BNNS composite exhibited a relative thermal conductivity enhancement of 191%. Moreover, both of materials demonstrated significantly improved thermal stability, with slightly reduced breakdown strength. Mechanical property testing revealed a maximum increase of 187.5% in fracture elongation. Highlights: Comprehensive study on curing agent modified hBNHigh dispersion of BNNS after wet ball millingModified BNNS improves composite interface propertiesThe thermal conductivity increases twice under 10 wt% BNNS loadingComposite materials with outstanding electrical insulation and high fracture elongation [ABSTRACT FROM AUTHOR]

In the present work, a lot of efforts have been made to reduce the sulfur particles, as main pollutants, from gasoline with using cerium (Ce) and Al(NO3)3 nano composites measured with Reference method: ASTM D7039‐15. The sulfur crystallite number was around 7235 ppm for DS (Ni (NO3)2 and urea). These unwanted sulfur particles reached to 3028 ppm for y (Al (NO3)3)/x (Ce)=0.25 in weight ratio, without using centrifuge process. This result is a very good due to some points: The present experimental works have been done at the room temperature and atmosphere environment, whilst many other works, as addressed here, have needed higher temperature and pressures. To our knowledge, Ce, Aluminum nitrate and urea as nano composite materials have need been used for desulfurization processes. Moreover, some relevant techniques such as X‐ray powder diffraction (XRD), Energy dispersive X‐ray analysis (EDX), Fourier Transform Infrared (FTIR) spectroscopy, X‐ray photoelectron spectroscopy (XPS), UV‐Vis spectroscopy, transmission electron microscopy (TEM), and Dynamic light scattering (DLS) have also been used. [ABSTRACT FROM AUTHOR]

Room temperature gas sensing is crucial for practical devices used in indoor environments. Among various materials, metal oxides are commonly used for gas sensing, but their strong insulating properties limit their effectiveness at room temperature. To address this issue, many studies have explored diverse methods such as nanoparticle decoration or conductive support, etc. Here, we report the emergence of gas-sensing functionality at room temperature with improved CO gas selectivity on SnO2 nanoparticles through sequential steps by using amorphous carbon (a-C) support and PtOx decoration. The SnO2 decorated on amorphous carbon shows enhanced gas adsorption compared to inactive gas sensing on SnO2 decorated carbon support. The higher Vo site of SnO2 on a-C induces gas adsorption sites, which are related to the higher sp2 bonding caused by the large density of C defects. The ambiguous gas selectivity of SnO2/a-C is tailored by PtOx decoration, which exhibits six values of sensing responses (Rg/Ra or Ra/Rg) under CO gas at room temperature with higher selectivity. Compared to PtOx/a-C, which shows no response, the enhanced CO gas sensing functionality is attributed to the CO adsorption site on PtOx-decorated SnO2 particles. This report not only demonstrates the applicability of CO gas sensing at room temperature but also suggests a strategy for using SnO2 and carbon compositions in gas sensing devices. [ABSTRACT FROM AUTHOR]

Polyaniline−magnesia (PANI/MgO) composites with a fibrous nanostructure were synthesized via in situ oxidative polymerization, enabling uniform MgO integration into the polyaniline matrix. These composites were characterized using FTIR spectroscopy to analyze intermolecular bonding, XRD to assess crystallographic structure and phase purity, and SEM to examine surface morphology and topological features. The resulting PANI/MgO nanofibers were utilized to develop ammonia (NH3) gas-sensing probes with evaluations conducted at room temperature. The study addresses the critical challenge of achieving high sensitivity and selectivity in ammonia detection at low concentrations, which is a problem that persists in many existing sensor technologies. The nanofibers demonstrated high selectivity and optimal sensitivity for ammonia detection, which was attributed to the synergistic effects between the polyaniline and MgO that enhance gas adsorption. Furthermore, the study revealed that the MgO content critically influences both the morphology and the sensing performance, with higher MgO concentrations improving sensor response. This work underscores the potential of PANI/MgO composites as efficient and selective ammonia sensors, highlighting the importance of MgO content in optimizing material properties for gas-sensing applications. [ABSTRACT FROM AUTHOR]

Nanomaterials have garnered significant attention in recent years for their potential to enhance the mechanical properties of cementitious construction materials, particularly in high-strength concrete applications. This review aims to explore the effects of various types of nanomaterials on the mechanical properties of concrete materials. Current developments in the synthesis, characterization, and use of nanomaterials in the field of cementitious materials are thoroughly examined in this review. The incorporation of various nanomaterials such as nano-silica, nano-titania, carbon nanotubes, nano-clay, and nano-alumina can significantly enhance the mechanical properties of cementitious construction materials, particularly in high-strength concrete applications. These nanomaterials contribute to denser microstructures, improved hydration products, and enhanced interfacial bonding within the cement matrix, ultimately leading to superior mechanical performance. However, proper dispersion, dosage, and compatibility considerations are essential to realize the full potential of nanomaterials in cementitious materials. The optimum % of NS in cement was reported to be between 1 and 8%, whereas the optimum % of graphene oxide (GO) in cement was reported to be only between 0.05 and 0.5%, imparting high strength characteristics to concrete. The findings of the study promote the use of nanoparticles in cement concrete to enhance the strength of high-rise concrete buildings. The results of various studies are compared, and some significant recommendations are also made. Furthermore, this research underscores the practical applications of nanocomposite-based concrete materials while acknowledging their limitations and opportunities. [ABSTRACT FROM AUTHOR]

AbstractIn several industries, the handling of fluid-filled micropipes is common. New-brand structures are increasingly being manufactured using advanced materials. This article tackles one of the crucial dynamic analyses that an advanced fluid-filled micropipe encounters. The dynamics of a graphene nanoplatelets-reinforced micropipe (GPL micropipe) under pulsating laminar flow for the first time is examined. The Euler-Bernoulli beam model follows the modified couple stress theory (MCST) and von-Karman’s nonlinear strain to formulate the problem. The impression of the flow profile exerted by a real flow as a consequence of fluid viscosity, is taken into account. The plug flow model results are compared to those regarding real flow consideration. Using the method of multiple scales (MMS), we determine the instability area and the steady state response of the GPL micropipe subjected to the principal parametric resonance of one of its modes due to pulsating laminar flow by applying this method to the discretized couple nonlinear gyroscopic governing equations. The Floquet theory treats the linear equations and fourth-order Runge–Kutta (RK4) method attacks nonlinear ones to validate MMS findings. It is confirmed that the 0.3% addition of the GPL to matrix phase significantly enhances its advanced attributes, making it a highly effective material. The GPL reinforcement phase in the FGO pattern increases the critical flow velocity that exhibits the micropipe to static instability by 37.98%, and critical flow stimulation amplitude fraction by 152.19%, while declines instability area bandwidth by 36.95%, and steady state response by 67.17% relative to a non-reinforced micropipe. A denser flow degrades the corresponding values by 18.40%, 42.59%, 41.67%, and 227.28% in comparison to a lighter fluid. The declared findings provide crucial insights into the key design elements affecting significantly the functioning of fluid-filled GPL micropipes system, and regulate future research and expand openings for industry applications. [ABSTRACT FROM AUTHOR]

Intrinsically stretchable conductors are vital components in next‐generation flexible electronics. However, solid conductive networks are generally vulnerable to external deformations due to their incompatible mechanical properties with the highly elastic substrates or matrixes. It is still challenging to achieve precisely controlled conductive structure with stable electromechanical performances. Herein, a nanocomposite conductor with 3D engineered bicontinuous phase system is developed, which is constructed by alternately arranged robust solid‐phase and conductive liquid‐phase via additive liquid/solid assembly. The proper rheological properties and extraordinary structural compatibility of the liquid‐phase prompt the formation of bridged structure within the 3D periodic solid‐phase main skeleton, giving rise to stable and even strain‐enhanced electrical and electromagnetic interference (EMI) shielding properties under external deformation. A negative resistance change of −37% along with unabated EMI shielding effectiveness and mechanical properties are obtained at 100% strain, showing negligible performance degradation even after 10,000 cycles of rigorous stretching and releasing. A strain‐tolerant pressure‐sensing device is further demonstrated using the liquid/solid nanocomposite structure, delivering a unique function of precisely recognizing the local pressure at large tensile loading interference. This work provides a new paradigm for the manufacturing of nanocomposites with desired functionalities using the adequate nanofiller reserve toward practical strain‐tolerant applications. [ABSTRACT FROM AUTHOR]

Highlights This study evaluated the percolation threshold in polymer nanocomposites and its dependence on the aggregation/agglomeration phenomenon. The main objective of the investigation was to propose a particular method that besides revealing the impact of different involved parameters on the percolation threshold could also provide useful information regarding the system characteristics. In line with that, a specific geometrical structure was employed to represent the clusters and assess the variation of the percolation threshold and characteristics of the polymer/particle interphase region. The findings were applied in an improved form of the percolation theory to perform validation against the related experimental data. Improvement was conducted by involving the impact of the newly estimated percolation threshold, aggregations/agglomerations, interphase region, and so forth. Also, specific theories were employed to define the electrical conductivity of the nanoparticle clusters and interphase region. The results showed that the percolation threshold is directly affected by the content of the nanoparticles and the characteristics of the aggregates/agglomerates. Besides, it was revealed that parameters, such as the size of nanoparticles, physical characteristics of the polymer matrix and interphase region, dispersion quality, etc. may substantially affect the percolation threshold and subsequently other physical properties of the system, such as electrical conductivity. A structural approach toward understanding the percolation phenomenon. Defining the particular dependence of percolation threshold on dispersion quality. Estimating the content of aggregates/agglomerates using percolation theory. Improving the percolation theory to predict the electrical conductivity. Applying the scaling theory to define the electrical conductivity of the interphase. [ABSTRACT FROM AUTHOR]

Highlights The demand for polymers with antibacterial properties is increasing in food packaging industry and medical supplies. Antibacterial additives without toxic metal ion release are crucial for health and safety but still have challenges. Herein, polypropylene (PP) nanocomposite was prepared with polyaniline/graphene nanocomposite (PANI/GNP) as a green antibacterial additive due to its electrostatic, free radical, and nanoknife effect synergistic antibacterial mechanisms. To improve the dispersibility of PANI/GNP, nanosilica coating on PANI/GNP was constructed successfully with in situ condensation polymerization of epoxy functionalized ethyl orthosilicate to obtain EP‐nSiO2‐PANI/GNP. EP‐nSiO2‐PANI/GNP with a thin nanosilica coating has a significantly improved thermal stability as compared with that of PANI/GNP characterized by TGA. The EP‐nSiO2‐PANI/GNP presents a nanoscale disperse state in PP nanocomposite and thus enhances the melt viscosity and storage modulus accordingly characterized by TEM and Rheology. The EP‐nSiO2‐PANI/GNP/PP filled with 0.5 wt% of EP‐nSiO2‐PANI/GNP demonstrates antibacterial activity of 100% against both Escherichia coli and Staphylococcus aureus. In situ condensation polymerization to prepare EP‐nSiO2‐PANI/GNP. EP‐nSiO2‐PANI/GNP has enhanced dispersion stability. EP‐nSiO2‐PANI/GNP with a thin nanosilica coating has a good thermal stability. PP nanocomposite with 0.5 wt% filler has excellent antibacterial activity. The electrostatic, free radical, and nanoknife effect antibacterial mechanism. [ABSTRACT FROM AUTHOR]

Treating dye-containing wastewater poses numerous challenges due to its high chemical complexity and its persistent nature. Thus, the present study aims to synthesize biochar derived from banana peel (BC) and its nanocomposites with copper oxide nanoparticles (CuOx/BC1-x) for the purpose of adsorptive removing Congo red (CR) dye from water. Several analytical methods were utilized to describe the physicochemical features of the CuOx/BC1-x nanocomposites. It was found that the crystallinity of the nanocomposites gradually improved, while the specific surface area and the surface electronegativity were reduced with increasing x value. The effects of x values (0–0.5), interaction time (10–120 min), adsorbent dose (0.01–0.05 g), initial CR concentration (20–200 mg/L), and the solution temperature (20–60 °C) were evaluated on CR removal. The obtained results revealed that the CuO0.5/BC0.5 nanocomposite showed the highest adsorption efficiency with a maximum adsorption capacity of 233.6 mgg−1. Analysis of the equilibrium experimental data revealed that the Langmuir and the pseudo-2nd-order models were the most proper to describe the current adsorption process. Moreover, the thermodynamics studies demonstrated that the adsorption process was spontaneous, endothermic, and random. [ABSTRACT FROM AUTHOR]

Rubber nanocomposites exhibit strain softening under large‐amplitude oscillation shear and large‐strain cyclic tension while the softening behaviors are hard to regulate in industry. Herein, an oligomer deep eutectic solvent (DES) synthesized from polyethyleneglycol and tetrabutylammonium bromide is used to mediate the vulcanization and softening behaviors of natural rubber (NR) gums and their nanocomposites. The results show that DES could accelerate NR vulcanization and improve crosslinking density. For the hydrophilic silica nanocomposites, DES could greatly reduce tanδ and weaken weak strain overshoot accompanying Payne and lower percentages damping accompanying Mullins effects. The effects in nanocomposites filled with hydrophilic/hydrophobic silica and carbon black are investigated and compared. The investigation provides a new way for tailoring elasticity and dissipation of vulcanizate nanocomposites filled with hydrophilic silica. [ABSTRACT FROM AUTHOR]