Nanocomposite Materials Research Articles

Application of edible nanocomposites from chitosan/fenugreek seed mucilage/selenium nanoparticles for protecting lemon from green mold

Green (Penicillium digitatum) mold can severely endanger the citrus fruits production and quality. Targeting the protection of lemon fruits from green mold infestations with nanobiotechnology approach, the fenugreek seed mucilage (FM) was extracted and exploited for biosynthesis of selenium (SeNPs) nanoparticles; their nanocomposites (NCs) with chitosan (CT) was constructed and employed as antifungal materials and edible coating (ECs) to protect lemon fruits against green mold. The nanoparticles formation and conjugations were verified by infrared (FTIR) analysis and electron microscopy. The FM-synthesized SeNPs had particles average of 8.35 nm, were the NCs of them with CT had size mean of 49.33 nm and charged with +22.8 mV. The CT/FM/SeNPs composite exhibited superior antifungal actions toward P. digitatum isolates, up to 32.2 mm inhibition diameter and 12.5 mg/mL inhibitory concentration, which exceeded the actions of imazilil. The microscopic screening of exposed P. digitatum to NCs clarified their mycelial destructive action within 30 h. The coating of infected lemons with fabricated NCs led to complete elimination of green mold development after 10 days of coating, without any infestation remarks. The innovative fabrication of NCs from CT/FM/SeNPs is strongly suggested to protect citrus crops from green mold and preserve fruits quality.

Multi-approach synthesis of functionalized graphene oxide as reinforcement for polyethylene: Make a strong interaction

Nanoparticles need to be well dispersed in a polymer matrix to employ their advantages. Their agglomeration may cause defects and stress concentrations, deteriorating the final properties of polymer/graphene nanocomposite. Here graphene oxide (GO) was functionalized in several ways to improve its interaction with polyethylene and dispersion. Polyethylene-grafted maleic anhydride (PE-g-MA) with strong polar groups was used as the matrix to consider a high potential of enhanced interaction with the GO nanoparticles and therefore obtain a high-performance polyolefin composite. First, GO was produced by modified Hammer’s method from graphite. The GO was aminated by phenylene diamine and named FGO. Also GO was reduced chemically to obtain CRGO and thermally to obtain TRGO and then the recent ones were amino functionalized, named FCRGO and FTRGO, respectively. In another route GO was first amino functionalized and then was reduced chemically and named FCRGO+. The synthesized nanoparticles were characterized by visual tests, FTIR, XRD, SEM, and TGA analysis. Subsequently, the study investigates the fabrication of nanocomposites using these nanoparticles at 2 wt% in the PE-g-MA matrix by solution-casting method. The nanocomposites were characterized by optical microscopy, tensile and rheometric tests, FTIR, DSC, and SEM analysis. Based on the results, FCRGO+ was identified as the optimum nanoparticle having better dispersion, improved interfacial interaction, and stronger mechanical properties. The GO functionalized nanocomposites showed up to 36% in tensile modulus, 56% in tensile strength and 70% in elongation at break as compared to those of GO nanocomposites without functionalization of GO.

Facile synthesis of novel porphyrin-based covalent organic frameworks integrated with Au nanoparticles for highly sensitive detection of organophosphorus pesticide residues

Organophosphorus pesticides (OPs) residues in agricultural products such as vegetables, fruits, and grains pose a threat to food safety and human health. In this work, a novel and highly sensitive electrochemical biosensor was developed for OPs residues detection in real sample, based on the immobilization of acetylcholinesterase (AChE) by electrostatic adsorption on a glassy carbon electrode (GCE) modified with composite nanomaterials of porphyrin-based covalent organic frameworks (p-COFs) loaded by gold nanoparticles (AuNPs) and poly (diallyldimethylammonium chloride) (PDDA). Due to the synergistic effect of p-COFs, AuNPs and PDDA, the fabricated biosensor displayed the remarkable properties with the high electrocataytic activity, and excellent biocompatibility, resulting in a significant signal amplification of as-prepared biosensor. Under optimized conditions, the biosensor showed excellent sensing performances for the detection of methyl parathion (MP), with wide linear ranges from 1.9 × 10−9–3.8 × 10−5 M and a low detection limit as low as 2.3 × 10−10 M, as well as the satisfactory selectivity, excellent reproducibility, anti-interference properties and good stability. It was also successfully applied to the monitoring of MP content in vegetables and fruits, which may be explore a new opportunity for the potential utilization in analysis field.

Samarium-doped vanadium pentoxide nanorods anchored reduced graphene oxide nanocomposite as a bi-functional electrode material for supercapacitor and direct methanol oxidation fuel cell applications

In this work, we demonstrate a novel, facile synthesis of reduced graphene oxide nanosheets decorated samarium-doped vanadium pentoxide (RGO/Sm:V2O5) nanocomposite material and explore its application toward supercapacitor and direct methanol oxidation process. As-fabricated material and electrode were well-characterized to evaluate its surface morphology and functionalities. Results indicate a maximum capacitance value of 544 F/g for RGO/Sm:V2O5 modified electrode than the 2% Sm:V2O5 (346 F/g) and V2O5 (133 F/g) modified electrodes. In addition, an excellent Rct value (3.2 Ω) was achieved for the RGO-loaded Sm:V2O5 electrode than the 2% Sm:V2O5 electrode (4.7Ω). The RGO/Sm:V2O5 electrode also shows higher cyclic efficiency (98 %) at the 1000th cycle than the non-RGO loaded Sm:V2O5 electrodes. Furthermore, the fabricated electrodes were also examined for the direct methanol oxidation performances, and the results indicate a higher current density value of 181 mA/cm2 for RGO/Sm:V2O5 electrode than 2% Sm:V2O5 electrode (139 mA/cm2). The excellent electrochemical performance of the RGO/Sm: V2O5 electrode is mainly due to the presence of RGO nanosheet in the synthesized nanocomposite material. Therefore, as-prepared material can be applied as an excellent alternative electrode material for energy storage and conversion systems.

Facile synthesis of a carbon supported lithium iron phosphate nanocomposite cathode material from metal-organic framework for lithium-ion batteries

Lithium iron phosphate (LiFePO4, LFP) has become one of the most widely used cathode materials for lithium-ion batteries. The inferior lithium-ion diffusion rate of LFP crystals always incurs poor rate capability and unsatisfactory low-temperature performances. To meet with the requirements from the ever-growing market, it is of great significance to synthesize carbon supported LFP nanocomposite (LFP/C) cathode materials using cost effective and environmentally friendly methods. In this work, an LFP/C cathode material is straightforwardly prepared from a metal–organic framework (MOF) precursor ferric gallate (Fe-GA) using its self-template effect. The Fe-GA precursor is firstly fabricated from the redox coprecipitation reaction between Fe foils and gallic acid (GA) molecules in mild aqueous phase. Then the Fe-GA is directly converted to the LFP/C sample after a following solid-state reaction. In half-cells, the LFP/C composite exhibits a reversible capacity of 109.7 mAh·g−1 after 500 cycles under the current rate of 100 mA·g−1 at 25 °C as well as good rate capabilities. In the LFP/C//graphite full-cells, the LFP/C composite can deliver a reversible capacity of 71.4 mAh·g−1 after 50 cycles in the same condition as the half-cells. The electrochemical performances of the LFP/C cathode in half-cells at lower temperature of −10 °C are also examined. Particularly, the evolution of samples has been explored and the lithium-ion storage mechanism of the LFP/C cathode has been unveiled. The sample synthesis protocol is straightforward, eco-friendly and atomic efficient, which can be considered to have good potential for scaling-up.

Frontal Polymerization for the Rapid Obtainment of Polymer Composites.

Among the different polymerization techniques, frontal polymerization (FP) has gained high interest from the scientific community because of its peculiar characteristics: in particular, compared to classic polymerization reactions, FP allows for a better exploitation of the heat of polymerization involved, without requiring any external energy input apart from an initial photo or thermal ignition that triggers the reaction. The latter usually propagates in a few tenths of seconds or (at most) minutes through a hot self-sustaining polymerization front, giving rise to the formation of fully cured thermosetting networks or thermoplastic polymers. Furthermore, different polymerization mechanisms can be involved in FP reactions, comprising cationic or anionic, ring-opening metathesis, and free-radical polymerization, among others. Further, it is possible to run FP reactions in bulk, in solution, or even using solid monomers if they are melted at the temperature of the front, notwithstanding the possibility of using reactive systems containing fillers or fiber/fabric reinforcements. In this context, the use of FP is becoming very important also for the design and production of advanced (nano)composite materials, saving processing time and achieving the completeness of the curing reaction, even in the presence of high filler/reinforcement loadings. Therefore, this mini-review aims to provide the reader with the basics of FP and its main peculiarities, even in the context of preparing high-performing composites. In this respect, some recent case studies witnessing the potentialities of frontal polymerization for the design of advanced (nano)composite systems will be elucidated. Finally, some perspectives about possible future developments will be proposed.

Comparative analysis of machine learning techniques for predicting wear and friction properties of MWCNT reinforced PMMA nanocomposites

Polymer nanocomposites have received significant scientific and industrial attention due to the synergetic combination of features of a polymeric matrix and organic or inorganic nanofillers. While experiments have been essential for identifying and characterizing new materials, their high costs and limited trials have shifted the focus towards applying machine learning (ML) to predict nanocomposite properties. This study aims to establish a connection with the tribological performance of multi-walled carbon nanotubes (MWCNT) reinforced with polymethyl methacrylate (PMMA) nanocomposites through the comparison of ML techniques. The wear and friction characteristics of MWCNT-reinforced PMMA nanocomposites were predicted based on three input variables: material weight percentage, load weight, and track diameter. The features of nanocomposites were predicted using three different ensemble ML algorithms: random forest (RF), extra tree (ET), and gradient boosting machine (GBM). The dataset was utilized to train the proposed models in Python, followed by hyperparameter tuning to determine the best model for predicting target values. The results demonstrated that the GBM model outperformed the RF and ET models, with an R-squared of 0.99, RMSE of 0.62, and MAE of 0.18. The proposed models’ predictions of wear values were more precise than their friction values. These findings indicate that ML techniques, particularly the GBM model, can effectively predict the tribological properties of MWCNT-reinforced PMMA nanocomposites, potentially reducing the need for extensive experimental trials and contributing to advancements in nanocomposite material science.

High performance La1-xAlxF3 nanocomposite coatings prepared by a co-evaporation technique

La1-xAlxF3 nanocomposite coatings with various amounts of AlF3 in LaF3 were deposited on the fused silica substrate using double-source electron beam co-evaporation. The effects of the material composition on the chemical composition, optical properties, microstructure properties, and residual stress of these deposited coatings were investigated. The results showed that although the doping of AlF3 led to a reduction in the refractive index, the overall performance of the nanocomposites showed remarkable improvement. The increase in the AlF3 content of prepared nanocomposites caused a decrease in the crystallinity, surface roughness, residual stress, and optical loss. Compared to polycrystalline LaF3, the La1-xAlxF3 nanocomposite (x ≥ 0.3) retained an amorphous structure, showcasing smooth surface morphology and lower absorption. As a result, the total optical loss was reduced. Additionally, the tensile stress was also mitigated to a certain extent, which means that the nanocomposite material was less prone to cracking. Finally, a 193 nm-La0.70Al0.30F3/AlF3 high reflective coating was prepared, which achieved an improved reflectance of 98.7% and better film quality compared to the pure LaF3/AlF3 sample. These findings clearly indicate the significant potential of La1-xAlxF3 nanocomposites for developing deep ultraviolet band thin films, extending even into the vacuum ultraviolet band.

Supported copper nanoarchitecture for selective ethylbenzene oxidation (EBO) reaction

Copper-based (Cu-NP) uniformly dispersed on various inorganic supports (alumina, silica, titania, and zirconia) were prepared by the reverse microemulsion technique. These nanoparticles were used for the selective oxidation of ethylbenzene (EB) to produce acetophenone (AP) as the main product in the presence of Tert‑butyl hydroperoxide(TBHP) as an oxidant. This study focused on creating Cu-nanoparticles evenly dispersed on alumina using varying Cu-loadings (5 %, 10 %, and 15% wt.) and Brij-35 as the surfactant. The resulting catalytic material was characterized using various physicochemical techniques like XRD, FESEM, HRTEM, XPS and physisorption techniques. Various parametric studies were conducted, such as the effects of temperature, catalyst support, catalyst loading, and TBHP loading to optimize the EB conversions and AP selectivity. Among the various catalyst loadings, 15 % CuO/Al2O3 (15 % of the copper content) nanocomposites showed exceptional performance, with the highest EB conversion rate (99.7 %) and AP selectivity (98.5 %) compared to other nanocomposites. The catalyst's stability and recyclability over four cycles were attributed to the strong copper oxide-alumina interaction. These findings suggest that this nanocomposite material is a promising candidate for catalytic applications, offering high selectivity and consistent EB conversion rates.

The Electromagnetic Shielding Properties of Biodegradable Carbon Nanotube–Polymer Composites

In this article, the electromagnetic shielding properties of carbon nanotube–polymer nanocomposites are presented. The composite fabrication technique is spray-drying, the usage of which leads to a uniform dispersion of carbon nanotubes (CNTs) in a polymer matrix. Obtaining good filler dispersion is necessary to form a continuous, electrically conductive network of CNTs inside the polymer matrix. In the described nanocomposites, the network of conductive filler particles acts as an electromagnetic radiation barrier. For this reason, developing a highly effective fabrication method is very important. Also, the method should be simple enough to be easily adopted in an industrial environment. The authors shows in this text that both goals mentioned are achieved. The obtained nanocomposite material not only has electrostatic shielding capabilities but comprises electromagnetic shielding properties, which fulfills the main goal of the presented work. It is also worth mentioning that the developed manufacturing method allows for the usage of different fillers and polymers and thus the fabrication of materials capable of meeting a wide range of requirements.

Preparation and performance study of polyurethane/ kaolinite nanocomposite insulation materials

Abstract Polyurethane foam insulation materials exhibit excellent noise reduction, shock absorption and vibration damping capabilities while being cost-effective and easily moldable. They have found widespread applications in diverse fields such as automotive, machinery, packaging, insulation, healthcare and construction. However, the application range of this traditional organic material is limited by issues related to thermal stability and flame retardancy. By achieving uniform dispersion of nanoparticles, composite materials exhibit enhanced comprehensive properties in terms of flame retardancy, oxidation resistance, physicochemical stability and structural performance. Polyurethane/Kaolinite nanocomposite insulation materials were prepared by using the in situ intercalation compounding method. X-ray diffractometer, Fourier infrared spectrophotometer, thermogravimetric analyzer and scanning electron microscope were used to characterize the thermal stability of the composite material obtained under different preparation conditions and the state of the nanomaterial in the system. The results showed that the composite material with good dispersion of kaolinite in the matrix was obtained by effective surface modification through dimethyl sulfoxide. The doping of low-concentration kaolinite can improve the thermal stability of polyurethane. When the mass fraction of nano-kaolinite is 5%, the initial decomposition temperature of the composite system is 47°C higher than that of pure polyurethane and the system achieves the highest thermal stability.

Enhanced supercapacitive performance of FeAl2O4/g-CN nanocomposite for advanced energy storage systems

The innovation of nanomaterials for supercapacitors (SCs) presents a potentially viable solution to the energy crisis arising from our excessive dependence on fossil fuels. The present study demonstrated the hydrothermal synthesis of an environmentally sustainable and economical FeAl2O4 nanomaterial grafted on graphitic carbon nitride (g-CN) for supercapacitor applications. This study aimed to assess the supercapacitive capabilities of nanocomposite electrode material via various electrochemical tests. Upon investigation, it was discovered that FeAl2O4/g-CN nanocomposite material demonstrated a remarkable specific capacitance (1049 F g−1), energy density (29 Wh kg−1) and power density (223 W kg−1). Furthermore, the inclusion of g-CN nanosheets into the FeAl2O4/g-CN nanocomposite which increased surface area (SAA, 46 m2 g-1), leading to a decrease in charge transfer resistance by 0.73 Ω. The enhanced electrochemical performance was attributed to many factors, including an increased SAA, greater number of active regions and a nitrogen-rich structure that facilitates rapid ion adsorption. The FeAl2O4/g-CN nanocomposite exhibited a robust pseudocapacitive characteristic and demonstrated exceptional conduction, leading to a significantly enhanced cyclic stability endurance of 40 h. Hence, the synergistic behavior of FeAl2O4/g-CN nanocomposite results in its remarkable efficiency as a proactive electrode material for energy storage purposes.

Microstructural and mechanical properties evaluation of Calcium and zinc-modified WE43-based nanocomposites through stir casting for biodegradable applications

Magnesium-based alloys and composites have potential as biodegradable materials due to their moderate biodegradability, biocompatibility, and usefulness, but their mechanical strength limits their clinical use. The study synthesised a WE43-based alloy with calcium (Ca) and zinc (Zn), then reinforced it with nano reinforcements (hydroxyapatite, beta-tricalcium phosphate, graphene, and bioglass) through stir casting to create four nanocomposites. The microstructural and mechanical properties were examined to assess Ca and Zn's influence and determine the most effective reinforcement. The result showed that Ca and Zn-modified alloys and all nanocomposite materials have two additional phases, LPSO and Ca2Mg6Zn3, compared to the monolithic WE43 alloy. With the addition of Ca and Zn, S-2 saw significant increases in ultimate tensile strength (UTS), tensile yield strength (TYS), and uniform elongation (U.El), reaching ∼246 MPa, ∼144 MPa, and ∼8 %, respectively, while maintaining an elastic modulus of ∼19 GPa. This resulted in improvements of ∼29 %, ∼25 %, and ∼9 % compared to the as-cast WE43. Graphene-reinforced S-4 demonstrated superior mechanical properties with a UTS of 294 MPa, TYS of 194 MPa, U.El of ∼8 %, and an elastic modulus of 24 GPa, representing increases of ∼52 %, ∼69 %, and 6.05 %, respectively, compared to as-cast WE43. Additionally, S-4 exhibited impressive compressive properties, with an ultimate compressive strength (UCS) of 370 MPa, a compressive yield strength (CYS) of ∼185 MPa, and an U.El of ∼26 %. The bioglass-reinforced nanocomposites had a maximum hardness of 74.8 HV, whereas the as-cast WE43 had a maximum toughness of ∼4 J. These enhancements in mechanical properties are attributed to strengthening processes, including thermal mismatch, orowan, and grain refinement mechanisms. Graphene reinforcement shows promise for biodegradable applications.

Robust shape memory chlorobutyl rubber/boron nitride polymer nanocomposites for oil-water separation application

BackgroundBoron nitride (h-BN), an excellent 2D material finds exceptional applications in various fields owing to its unique characteristics including excellent hydrophobicity. Incorporation of boron nitride in polymer matrices is a captivating strategy by the scientific community to tune the properties of polymer. Interestingly, the possibilities of incorporating h-BN in chlorobutyl rubber (CIIR) matrix has never been considered and tried till now. Moreover, the use of CIIR to create a clean environment and reduce water pollution is an unexplored area even though the CIIR rubber possess excellent barrier properties. MethodsIn this work, two techniques were used for the fabrication of BNNS/CIIR nanocomposite. We exfoliated h-BN via chemical exfoliation method and tried the reinforcement of CIIR with BNNS via solution intercalation method. Shape memory analysis was performed with the help of stearic acid and oil-water separation analysis was achieved through an easy experimental technique. Significant findingsEnhanced mechanical strength of 11.57 MPa, improved thermal degradation temperature and char yield, higher glass transition temperature of -45.98° were observed for BNNS/CIIR nanocomposite reinforced with higher BNNS loading owing to the uniform distribution and better intercalation of BNNS in CIIR. Excellent shape memory was exhibited by CIIR matrix when reinforced up to 5 g BNNS. In addition, the nanocomposites displayed excellent ability to perform oil-water separation with increase in BNNS loading owing to the good hydrophobic character of h-BN and inherent barrier properties of CIIR. Thus, the study proved successful towards the fabrication of advanced CIIR nanocomposites with excellent shape memory and oil water separation efficiency.

Multifunction integration within magnetic CNT-bridged MXene/CoNi based phase change materials

Developing advanced nanocomposite phase change materials (PCMs) integrating zero-energy thermal management, microwave absorption, photothermal therapy and electrical signal detection can promote the leapfrog development of flexible wearable electronic devices. For this goal, we propose a multidimensional collaborative strategy combining two-dimensional (2D) MXene nanosheets with metal-organic framework-derived one-dimensional (1D) carbon nanotubes (CNTs) and zero-dimensional (0D) metal nanoparticles. After encapsulating paraffin wax (PW) in three-dimensional (3D) networked multidimensional MXene/CoNi–C, the resulting composite PCMs exhibit excellent thermal energy storage capacity and long-term thermally reliable stability. Benefiting from the synergistically enhanced photothermal effects of CNTs, Co/Ni nanoparticles and MXene, PW@MXene/CoNi–C can capture photons efficiently and transfer phonons quickly, yielding an ultrahigh photothermal conversion and storage efficiency of 97.5%. Additionally, PW@MXene/CoNi–C composite PCMs exhibit high microwave absorption with a minimum reflection loss of −49.3 ​dB at 8.03 ​GHz in heat-related electronic application scenarios. More attractively, the corresponding flexible phase change film can simultaneously achieve thermal management and electromagnetic shielding of electronic devices, as well as photothermal therapy and electrical signal detection for individuals. This functional integration design provides an important reference for developing advanced flexible multifunctional wearable materials and devices.

Combinational strategy of chemical graft and layer-by-layer assembly of novel nanocomposite membranes fabrication for heavy metal ion capture

Heavy metal ions (HMI), a non-degradable toxic substance, has raised widespread concerns in water purification. Membrane separation is a considerable and promising technology for removing HMIs from water, due to its environmentally friendly, clean and highly effective. This study reported a functional composite ultrafiltration membrane prepared from natural biomolecules ε-Poly-L-lysine hydrochloride (PLL), sodium lingo sulfonate (SLS) or sodium alginate (SA) based on the combination strategy of chemical graft and layer-by-layer assembly. The fabricated membrane exhibited a high pure water flux (2957 L·m−2·h−1), high capture efficiency for Cu2+ (99.1 %) and Pb2+ (98.9 %). Notably, the layer-by-layer assembly strategy provides abundant groups for HMI binding, ensuring the high capture efficiency. The fabricated membrane demonstrated a low flux decline (9 %), along with a high flux recovery ratio (99.2 %). Moreover, it exhibited exceptional stability and reusability across a wide pH range (pH 5–9), meanwhile maintaining a capture efficiency of approximately 99 % under near-neutral condition after undergoing 5 cycle experiments for both Cu2+ and Pb2+. Our work builds a straightforward approach for UF membrane fabricating with excellent HMI capture capacity, displaying the potential application in HMI waste water purification.

Green Synthesis of AgNPs and Fe2O3NPs Using Garlic Plant and Study their Anticancer Activity against Cervical Cancer Cells

In this study, silver and iron nanoparticles were biosynthesized using the garlic plant, an economical and environmentally friendly method. A blend of chitosan (CS) and polyvinylalcohol (PVA) was prepared. The silver nanoparticles (AgNPs), iron oxide nanoparticles (Fe2O3NPs), and the (CS/PVA) blend were characterized by X-ray diffraction (XRD), Fourier-transform infrared spectroscopy (FTIR), and Field Emission Scanning Electron Microscopy (FE-SEM) analyses. The FE-SEM images revealed that Fe2O3NPs were cubical and hexagonal, and AgNPs were spherical aggregates. AgNPs with blend (CS/PVA) and Fe2O3NPs with blend (CS/PVA) and (Fe2O3NPs/blend (CS/PVA) /AgNPs) composite were synthesized and tested for anticancer activity against cervical cancer cells (Hela) using the MTT assay. Best kills and the highest inhibitory effect were observed in (AgNPs/blend (CS/PVA)) and (Fe2O3NPs/Blend (CS/PVA)/AgNPs) composite. These findings demonstrated the method's ability to synthesize nanocomposites with desirable physical, chemical and biological properties. Therefore, these findings demonstrate the new antibacterial and robust cytotoxicity features of the nanocomposite material, which has promising medical applications.

Phase-field simulation of crack propagation in particulate nanocomposite materials considering surface stresses

Phase-field simulation of crack propagation in particulate nanocomposite materials considering surface stresses

Effective adsorptive uptake of hexavalent chromium ions from aqueous systems utilizing a superior activated nanobentonite@cobalt ferrite@carboxymethylcellulose nanocomposite

Contamination of industrial and dietary water with Cr(VI) ions is known as a global concern. Industrial wastes containing elevated Cr(VI) concentration are hazardous and harmful to people and animals, if inappropriately treated. Consequently, in the current research, a novel nanocomposite of activated nanobentonite@cobalt ferrite@carboxymethylcellulose (ANB@CoFe2O4@CMC) is generated and characterized. Several characterization techniques were employed to confirm the structure of as-prepared ANB@CoFe2O4@CMC. The mean particle size range of this nanocomposite was found to be 22.5–26.2 nm. Through batch adsorption assessments, ANB@CoFe2O4@CMC was employed and optimized to remove Cr(VI) ions from aquatic medium providing optimum conditions of pH 2.0, 25–30 min shaking time, 25 mg nanocomposite dosage at 25 °C reaction temperature. Freundlich model was extremely relevant via linear and nonlinear expression. Thermodynamic investigations were investigated to conclude that both exothermal and spontaneous tendencies in governing Cr(VI) adsorptive uptake. The ANB@CoFe2O4@CMC was remarkably stable after five subsequent runs of regenerating and recycling. This investigation displayed the potential of ANB@CoFe2O4@CMC as a powerful nanocomposite material for Cr(VI) recovery from diverse waters via a microcolum technique, exhibiting uptake values up to 87.9–95.8 %. As a result, the evaluated ANB@CoFe2O4@CMC could be successfully illustrated a superior material for effective multi-uptake Cr(VI) ions from water.

Enhanced electrochemical detection of chikungunya virus through aptasensor modification with origami paper-based ternary nanocomposite

Electrochemical sensors have drawn significant attention due to their crucial significance in the early detection of infectious illnesses, signifying their critical importance in diagnostic applications. This study’s proposed novel aptasensor exhibits a distinctive origami-based ePAD design, utilizing a unique silver-gold and zinc oxide (Ag-Au-ZnO) ternary nanocomposite for enhanced charge-transfer properties. Composite nanomaterials have a lower toxicity level, a higher signal enhancement capacity, increased sensitivity, improved conductivity, superior solubility, enhanced resolution capabilities, and a more straightforward functionalization process than individual nanomaterials. Employing paper, an economically advantageous substrate amenable to large-scale production with an origami-based ePAD is a critical enhancement of the sensor’s commendable attributes. Categorized as precision tools with an eco-conscious design, these sensors stand out for their streamlined manufacturing of environmentally sensitive substrates. This research capitalizes on the inherent foldability of paper to construct a three-dimensional multi-angular aptasensor, demonstrating cutting-edge specificity for chikungunya virus (CHIKV) detection. X- ray diffraction (XRD), Field emission scanning electron microscopy (FESEM), UV–vis spectroscopy, and Fourier transmission infrared spectroscopy (FTIR) characterized the nanocomposites. This study also includes aptamers as outstanding and sensitive instruments for quick diagnostic applications. With the use of Cyclic Voltammetry (CV), the analytical response of the aptasensor was carefully evaluated. The study demonstrates a broad linear detection range spanning from 1 ng/ml to 10 µg/ml, with an impressively low limit of detection (LOD) at 1 ng/ml for the CHIKV antigen (CHIKV-Ag), underscoring the novelty and heightened sensitivity of this aptasensor design. Moreover, the aptasensor successfully detects CHIKV antigens in serum samples, and a long stability test demonstrates its practical utility and long-term stability for clinical applications. The proposed study concludes by introducing a novel origami-based paper-based analytical device (ePAD) as a promising tool for the quick, precise, and selective identification of the CHIKV antigen as well as its affordability, easy fabrication, and suitability of POCT testing makes an excellent diagnosing technique in resource-limited settings.