Polymer Blend Matrix Research Articles

Green synthesis of boehmite-reinforced cashew gum/polypyrrole biopolymer blend for advanced biomaterials

Electrically conducting biopolymer blend nanocomposites based on different contents of boehmite (BHM) reinforced cashew gum (CG) /polypyrrole (PPy) blend is synthesized by an in situ polymerization technique using water as a green solvent. The resulting bio-blend nanocomposites underwent comprehensive analysis concerning their structural, morphology, thermal, and electrical properties, such as dielectric constant, dielectric loss, electric modulus, and AC conductivity. The Fourier transform infrared spectroscopy (FTIR) spectra revealed the presence of metal oxide stretching in the blended nanocomposite at 512 cm−1. Field emission scanning electron microscopy (FE-SEM) confirmed the attachment and uniform dispersion of BHM within the CG/PPy blend at 7 wt% loading, and beyond this loading, the nanoparticles get agglomerated in the biopolymer blend. The glass transition temperature and thermal stability of all the blended nanocomposites are higher than that of the pure CG/PPy blend and these thermal properties increase with the loading of nanoparticles. Conductivity experiments demonstrated that as the nanofiller content increases up to 7 wt%, there is a concurrent rise observed in AC conductivity, dielectric loss, and dielectric constant. There is a substantial difference of 1.21 Scm−1 between the maximum and minimum AC electrical conductivity, at 102 Hz. However, a decrease in electrical properties is observed at the highest loadings of BHM due to the agglomeration of nanoparticles in the polymer blend matrix. The lowest activation energy value (0.049 × 10−4 eV) is also exhibited by 7 wt% BHM nanocomposites. Furthermore, the electrical properties of both CG/PPy and CG/PPy/BHM nanocomposites exhibited a temperature-dependent behavior, progressively increasing until reaching maximum values. This study suggests that such bio-based polymer dielectrics could be promising materials for various applications, offering enhanced thermal and electrical properties through careful control of nanofiller content and dispersion.

Preparation and optimization of nanocomposite membranes for ethanol dehydration via pervaporation by using response surface methodology

BackgroundAlcohol dehydration using pervaporation, as a fast-developing process, requires more facilitation by improving their membrane performance. MethodsGraphene oxide nanosheets (GONs) were incorporated into blend matrixes of chitosan (CS) and polyvinyl-alcohol (PVA) to prepare nanocomposite membranes (NCMs) for ethanol dehydration. The membranes' structure was evaluated using SEM and FTIR analysis and their dehydration performance was studied against membrane composition (GONs loading and the CS/PVA blending ratio) and operational variables (feed temperature and ethanol concentration) using response surface methodology. Significant FindingsSEM images revealed GONs uniform dispersion within the membrane matrix and the FTIR results revealed the hydrogen bonds formation and minor changes after GONs incorporation. The optimum NCM was selected as 50 wt. % CS/PVA blended polymer matrix loaded by 4 wt. % GONs with permeation flux (PF) and separation factor (SF) were improved by 50 % and 5-fold, to 299 g/m2h and 1142. Its PF and SF reached 418 g/m2h (45 % increment) and 652 (30 % decrement) as its temperature elevated from 50 to 70 °C. These values were measured as 311 g/m2h (25 % decline) and 1106 (66 % improvement) by increasing the feed's ethanol content from 80 to 90 wt. %.

Synthesis of MnO@Fe2O3 core-shell doped PVA/PVP polymeric nanocomposites for electronic and optoelectronic devices: Mechanical, electrical, and optical properties

Abstract The aqueous solution cast method was utilized to create biodegradable nanocomposite of polymers (PNC) films from a poly (vinyl alcohol) / poly (vinyl pyrrolidone) blend (70/30 wt%) and MnO@Fe2O3 nFs. The dislocation density, particle size, and interplanar distance were all calculated. The PNC films' surface shape changes from smooth to porous and somewhat rough because of the nanosized MnO@Fe2O3 particles' dispersion in the blend matrix, which diminishes the blended crystallites' size. The composite film's tensile strength increased from 9.45 MPa for the pure (PVA-PVP) film to 22.35 MPa due to the addition of 6 wt% MnO@ Fe2O3. The optical band gap decreases from 5.26 and 4.84 eV for pure (PVA/PVP) blend direct and indirect energy band gap to 5.18 and 4.71 eV for comparable values of 6wt% MnO@Fe2O3 nFs. Up to 6 wt% MnO@Fe2O3 concentration, PNC films' dielectric permittivity first declines, but it is substantially identical to the pure polymer blend matrix. The PNC sheet's dielectric permittivity increases nonlinearly with temperature, although its DC conductivity follows the Arrhenius law. Laser power was attenuated by (PVA- PVP)/MnO@Fe2O3 for both He-Ne and solid-state green laser beams. When the MnO@Fe2O3 concentration in the blend matrix rises to 6 wt%, the output power for lasers with 532 nm and 650 nm wavelengths drops from 5.49 to 2.4 mW and 19.8 to 9.4 mW, respectively. The findings suggest that nanocomposites exist and are widely recommended for optoelectronics, microelectronics, radiation detection, and several other uses.

Flexible magnesium-ion-conducting solid poly-blend electrolyte films for magnesium-ion batteries

Solid biodegradable polymer electrolyte systems are considered the optimal choice for energy storage devices because they are both cost-effective and energy-efficient. A solid blend polymer electrolyte (SBPE) membrane capable of transporting magnesium ions was prepared using a mixture of 70 wt% methylcellulose, 30 wt% chitosan, and varying wt% magnesium perchlorate salt. X-ray diffraction analysis revealed an increase in the amorphous nature caused by the inclusion of Mg(ClO4)2 salt in the polymer blend matrix. A Fourier transform infrared spectroscopy study of samples containing varying salt concentrations revealed secondary interactions between polymer segments and salt, which provides the basis for energy density. Moreover, through impedance analysis, it was determined that the bulk resistance decreased with increasing salt concentration. The SBPE containing 30 wt% magnesium perchlorate exhibited the highest ionic conductivity, with a value of 2.49 × 10–6 S cm−1. A comprehensive evaluation of the ion transport parameters, including mobility, carrier density, and diffusion, was conducted for the prepared electrolyte samples. Notably, an ionic transference number (tion) of approximately 0.83 was observed for the SBPE sample with 30 wt% magnesium salt, indicating ions’ prevalence as the system’s primary charge carriers. Electrochemical analyses demonstrated that the SBPE with the highest ion conductivity possessed an electrochemical stability window (ESW) of 1.92 V. Additionally, the thermal characteristics of the samples were evaluated using thermogravimetric analysis (TGA) to assess the thermal stability of the electrolyte. Finally, the highest conducting polymer electrolyte was employed to construct a primary magnesium battery, and its discharge profile with different cathode materials was studied. Based on these findings, the current study suggests an environmentally friendly, biodegradable, and economically viable electrolyte option suitable for separator cum electrolytes in magnesium-ion batteries.

Development of halochromic labels based on binary systems of cationic guar gum and κ-carrageenan loaded with alizarin red S for monitoring milk and seafood freshness

Monitoring of food quality, in particular, high-protein food quality, is an important component in ensuring food safety and human health. In this research, a feasible and easy solution casting and solvent evaporation strategy was adapted to fabricate alizarin red S (ARS)-loaded halochromic cationic guar gum (CGG) and κ-carrageenan (CAR) blend packaging labels to improve its good physical strength, multifunctional acid–base responsive characteristics, and water barrier properties. The findings indicated that incorporating CAR at 40% polymer solid mass achieved higher tensile strength (21.0 ± 1.77 MPa), water resistance (29.92 ± 6.61% solubility), and thermal stability, which can be attributed to good compatibility between CGG and CAR. The results obtained from FT-IR, XRD, and SEM analyses demonstrate that the incorporation of ARS exhibits non-covalent bonding with the polymer blend matrix through electrostatic interactions and hydrogen bonding, thus reducing its crystallinity and restructuring the CGG-CAR matrix disorderly. The prepared indicating label films presented visual recognition of ammonia and trimethylamine (TMA-N) at 0.008 mM in 6 min (the total color difference (ΔE) for TMA-N is＞11.89), and can be reused at least six times. Moreover, the color of ARS at different pH values remains persistent for at least 180 days. The practical applications show that the films, as indicator labels, can realize real-time, accurate, and visual dynamic monitoring of seafood (shrimp) and milk by engendering three chromatic stages discernible by the naked eye (fresh, spoiling, and spoiled). The ΔE for monitoring sub-fresh milk and shrimp reached as high as 14.91 and 13.32, respectively.

Effect of SiC nanoparticles on mechanical and damping properties of epoxy/polysulfide rubber blend composite

Blend polymer matrix composite material are becoming more and more popular due to their promising mechanical properties. In this research, blend polymer mixture was make from epoxy resin (EP) blended with different weight percentages of polysulfide rubber (PSR) (0, 3, 6, 10, 15, and 20%). Then tensile, impact, bending strength and damping ratio were evaluated to get the high quality of mechanical properties for the blend matrix. Due to the requirements to enhance the mechanical properties of this blend; a various weight fraction of carbide silica (SiC) nanoparticle was used as a reinforcement in the ratios of (0, 1, 3, and 5%) by weight to the best ratio of the blended matrix. Tensile, impact, bending and damping ratio tests were also conducted to get the best mechanical properties for the blend materials. Experimental results for the blend matrix showed that adding polysulfide rubber to epoxy resin resulted in a decrease in Young’s modulus, tensile strength, and bending strength; however damping ratio and the impact strength increased. It is found that the weight fraction of 6% of PSR is the Better case, which gave the better mechanical characteristics properties for mixture. Utility of this mixture; it has intermediates between flexible properties of a mixture at the highest rate of PSR and brittle mechanical properties for EP resin. Mechanical and damping properties showed an increasing when the carbide silica (SiC) with a weight fraction of 3% added, then it decreased slightly.

Microporous Adsorbent-Based Mixed Matrix Membranes for CO2/N2 Separation

As the atmospheric carbon dioxide (CO2) concentration rapidly rises, carbon capture, utilization, and storage (CCUS) is an emerging field for climate change mitigation. Various carbon capture technologies are in development with the help of adsorbents, membranes, solvent-based systems, etc. One of the main challenges in this field is the removal of CO2 from nitrogen (N2) gas. This paper focuses on mixed matrix membrane technology, for which the CO2/N2 separation performance is based on differences in gas permeations. Membrane separation and purification technologies are widely studied for carbon capture. Microporous adsorbents such as zeolites and metal organic frameworks (MOFs) for carbon capture have been attracting researchers’ attention due to their highly porous structures, high selectivity values, and tunable porosities. Utilizing microporous adsorbents dispersed within a novel, blended polymer matrix, fourteen membranes were prepared with the commercial MOF ZIF-8, zeolite 13X, and kaolin, with methyl cellulose (MC) and polyvinyl alcohol (PVA), which were tested using a single gas permeation setup in this study. The addition of polyallylamine (PAH) as a chemisorbent was also investigated. These membranes were synthesized both with and without a polyacrylonitrile (PAN) support to compare their performances. MC was found to be an ideal polymeric matrix component to develop free-standing MMMs. At 24 °C and a relatively low feed pressure of 2.36 atm, a free-standing zeolite-13X-based membrane (MC/PAH/13X/PVA) exhibited the highest N2/CO2 selectivity of 2.8, with a very high N2 permeability of 6.9 × 107 Barrer. Upon the optimization of active layer thickness and filler weight percentages, this easily fabricated free-standing MMM made of readily available materials is a promising candidate for CO2 purification through nitrogen removal.

Fabrication and Characterization of Magnetic Nanoparticles-Embedded Polymer Blend Matrix of Sodium Alginate/Gellan Gum Beads for the Controlled Release of Amikacin Sulfate

Fabrication and Characterization of Magnetic Nanoparticles-Embedded Polymer Blend Matrix of Sodium Alginate/Gellan Gum Beads for the Controlled Release of Amikacin Sulfate

CO2-Philic Nanocomposite Polymer Matrix Incorporated with MXene Nanosheets for Ultraefficient CO2 Capture.

The incorporation of two-dimensional (2D) functional nanosheets in polymeric membranes is a promising material strategy to overcome their inherent performance trade-off behavior. Herein, we report a novel nanocomposite membrane design by incorporating MXene, a 2D sheet-like nanoarchitecture known for its advantageous lamellar morphology and surface functionalities, into a cross-linked polyether block amide (Pebax)/poly(ethylene glycol) methyl ether acrylate (PEGMEA) blend matrix, which delivered exceptional CO2/N2 and CO2/H2 separation performances that are critical to industrial CO2 capture applications. The finely dispersed Ti3C2Tx nanosheets in the blend polymer matrix led to an expansion of the free volume within the resultant mixed matrix membrane (MMM), giving rise to a substantially enhanced CO2 permeability of up to 1264.6 barrer, which is 102% higher than that of the pristine polymer. Moreover, these MXene-incorporated MMMs exhibited preferential sorption for CO2 over light gases, which contributed to an exceptional CO2/N2 and CO2/H2 selectivity (64.3 and 19.2, respectively) even at a small loading of only 1 wt %, allowing the overall performance to not only surpass the latest upper bounds but also exceed many previously reported high-performance nanosheet-based nanocomposite membranes. Long-term performance tests have also demonstrated the good stability of these membranes. This composite membrane design strategy reveals the remarkable potential of combining a blend copolymer matrix with ultrathin MXene nanosheets to achieve superior gas separation performance for environmentally important gas separations.

The Photocatalytic Performance of Ag /TiO2/Nylon 6/PMMA System

Herein, Ag/TiO2/Nylon 6/PMMA catalyst system was developed, and its photocatalytic properties were fully analyzed. XRD, SEM, EDS, and PL analyses were carried out to get information on crystal structure, micromorphology, elemental composition, and band gap energy. Photocatalytic degradation was followed by UV–vis spectrophotometry. The band gap of the catalyst was found to be between 2.51 and 3.1 eV. Up to 80% degradation was achieved under UV light irradiation. No bulk adsorption was observed, which means that the reaction was completely carried by the photocatalytic process. pH 3 value was determined to be suitable for a high rate. Reaction kinetic was determined to be matched with the first-order rate law. The newly developed polymer blend matrix system here may have broad application prospects in the remediation of water resources.

Nanocomposites comprising PVA/CMC matrix and CNTs/Fe2O3 nanohybrid: A comparative investigation of structural, optical, electrical, and dielectric properties as an application in advanced electrochemical and optoelectronic devices

This work addresses the fabrication of innovative flexible polymer nanocomposite films for electrochemical products made of poly (vinyl alcohol) (PVA), carboxymethyl cellulose (CMC), multi-walled carbon nanotubes (CNTs), and hematite (α-Fe2O3) nanoparticles (NPs) as nanohybrid. The PVA/CMC-CNTs/Fe2O3 nanocomposite films were characterized using various approaches. The PVA/CMC blend polymer matrix shows significant improvements in terms of amorphous nature with the CNTs/Fe2O3 nanofiller content, resulting in an exceedingly flexible polymer backbone and with higher ionic conductivity of the PVA/CMC-CNTs/Fe2O3 nanocomposites films, as reported by the XRD examination. The nanoparticle surfaces and the blend matrix exhibit a significant interaction, as seen by the FTIR spectra. To learn more about how CNTs/Fe2O3 NPs affect the optical characteristics of the PVA/CMC, its optical characteristics were examined. The absorption edge appeared to migrate towards lower photon energy sides upon the addition of CNTs/Fe2O3 NPs to the PVA/CMC matrix. The Eg (direct and indirect) of pure PVA/CMC was considerably decreased from 5.12 to 3.55 eV and 4.23 to 3.01 eV respectively by adding 3.5 wt% of CNTs/Fe2O3 NPs. The results proved the influence of the nanofiller on the host polymer's decreased band gap energy. The blend nanocomposite had a substantially higher AC conductivity compared with the blend, and the PVA/CMC-3.5%CNTs/Fe2O3 nanocomposite had the highest electrical conductivity. It was discovered that while the dielectric loss and dielectric constant increased with the high content of nanoparticles, they reduced with increasing frequency. These findings demonstrated that the produced films had undergone substantial changes, which allows for the use of flexible films made of PVA/CMC-CNTs/Fe2O3 in a variety of electrochemical and optoelectronic applications.

A comprehensive study on structural, optical, electrical, and dielectric properties of PVA-PVP/Ag-TiO2 nanocomposites for dielectric capacitor applications

Nanocomposites made from polymers and nanoparticles (NPs) have a wide range of uses. Herein, the polymer nanocomposite electrolyte films were prepared by blending polyvinyl alcohol (PVA) and polyvinylpyrrolidone (PVP) with hybrid NPs of silver (Ag) and titanium dioxide (TiO2). The structural, optical, electrical, and dielectric properties of the resulting PVA-PVP/Ag-TiO2 nanocomposite electrolytes were analyzed. XRD analysis revealed that the PVA-PVP blend had a semicrystalline structure, and the addition of hybrid NPs reduced the crystallinity ratio. FTIR analysis showed that the intensity decreased as the content ratio of hybrid NPs increased. Optical measurements showed that the nanocomposite electrolyte samples' direct and indirect optical energy gap decreased with the increasing content of hybrid NPs. The electrical conductivity also increased with the hybrid NPs' content, likely due to the higher conductivity of the hybrid NPs compared to the polymer blend matrix's electrical conductivity. The dielectric constant (εr) and dielectric loss (εi) increased with the concentration of hybrid NPs at lower frequencies, indicating the polarization effects of space charges. The capacitance–frequency (C–f) and conductance–frequency (G/ω–f) curves of the prepared polymer nanocomposites exhibited a discernible enhancement correlating with the increased content of Ag-TiO2 nanofillers. The impedance spectroscopy data were analyzed using Nyquist plots, which showed a single semicircular arc whose radius of curvature decreased with increasing the hybrid NPs loading, indicating a decrease in the overall impedance of the nanocomposite electrolytes with the mixed NPs loading. The impedance reduction and dielectric feature increase were attributed to the interfacial polarization between the hybrid NPs and the polymeric matrix. These findings suggest that the PVA-PVP/Ag-TiO2 nanocomposite electrolytes could be used for thin-film dielectric capacitor applications.

ИССЛЕДОВАНИЕ ТВЕРДЫХ ЭЛЕКТРОЛИТОВ НА ОСНОВЕ СМЕСИ ПОЛИМЕРОВ ПОЛИВИНИЛИДЕНФТОРИДА И ГИДРИРОВАННОГО БУТАДИЕН-НИТРИЛЬНОГО КАУЧУКА

The paper discusses the preparation of solid polymer electrolytes based on a blend of polyvinylidene fluoride and hydrogenated butadiene nitrile rubber with lithium bis(trifluorosulfonyl)imide prepared by solution casting technique. The films were characterized by X-ray diffraction analysis, FTIR spectroscopy, scanning electron microscopy, and differential scanning calorimetry. The influence of the polymer blend composition on the ionic conductivity of electrolytes was studied. According to the impedance spectroscopy data, it was found that the ionic conductivity of solid polymer electrolytes increases from 10-5 to 10-4 S/cm at room temperature with increasing the content of hydrogenated butadiene nitrile rubber up to 50 wt. % in the polymer blend matrix.

Unveiling the Synergy of Polymer–Salt Compositions for Properties Enhancement of Solid Polymer Electrolytes Based on PEO/PVP Blend Polymer Matrix and LiTFSI Dopant Salt

Solid polymer electrolytes (SPEs) are ion-dipole complexes credited to their use in the design and development of widespread solid-state ion conducting innovative devices. Accordingly, herein, two sets of highly flexible, stretchable, and sticky type SPE films based on poly(ethylene oxide) (PEO)/ poly(vinyl pyrrolidone) (PVP) blend as host matrix of different compositional ratios (i.e., 25/75, 50/50, and 75/25 wt/wt%) with 30 and 50 wt% lithium bis(trifluoromethanesulfonyl)imide (LiTFSI) as ionic dopant salt, and also one sample of polymer-in-salt (PiS) comprised the 50/50 wt/wt% polymer blend matrix and 60 wt% salt, are prepared and characterized in detail. These SPEs are predominantly amorphous having substantial absorbance for ultraviolet-visible radiations and tunable wide range energy band gaps. The 20 Hz—1 GHz broadband dielectric permittivity, loss angle tangent, and electrical conductivity spectra explained a variety of polarization and structural relaxation processes and the mechanism of ion transport ruled by the compositional synergy of polymer and salt in these SPEs. The highest ionic conductivity with appreciable electrochemical performance of the SPE is found for the PEO-rich blend matrix with 50 wt% of LiTFSI dopant. We conclude the suitability of these enhanced promising propertiesSPEs for the development of futuristic ion-conducting energy storage as well as revolutionary iontronic devices.

Polyimide blend metal–organic framework‐based mixed matrix membrane for gas separation: A review

AbstractPolyimide (PI), a glassy polymer, suffers from permeability–selectivity trade‐off and plasticization, which restrict its gas separation performance. Instead of exploring new materials, polymer blend and mixed matrix membrane (MMM) emerge as promising approaches in improving membrane gas separation efficiency attributed to their simplicity and cost efficiency. However, polymer immiscibility and polymer‐filler incompatibility are the main challenges encountered in these two approaches, respectively. Thus far, only limited reviews target the comparison between PI/glassy and PI/rubbery polymer blends. Besides, the review on improving the compatibility between polymer and filler in PI‐metal–organic framework (MOF) MMM is also lacking. Hence, this review aims to assess the gas separation characteristics of PI blended with glassy and rubbery polymers, focusing on the blend miscibility. It was discovered that the casting solvent's solubility parameter and solvent volatility play a part in governing the blend miscibility. Meanwhile, the efficiency of surface functionalization and ionic liquid addition in improving the polymer–filler compatibility in MMM is also reviewed. The wet method for filler incorporation demonstrates a more homogeneous filler dispersion within the membrane. Hence, its employment in MOF‐based MMM fabrication can be explored further.

Nanocomposite Solid Polymer Electrolytes with Polymer Blend (PVDF‐HFP/Pluronic) as Matrix and GO as Nanofiller: Preparation, Structural Characterization, and Lithium‐Ion Conductivity Analysis

AbstractNanocomposite solid polymer electrolytes (NSPEs) with PVDF‐HFP/Pluronic as blend polymer matrix, graphene oxide (GO) as nanofiller, and LiClO4 are reported. FTIR spectroscopy reveals the crystal phase transformation of PVDF‐HFP from nonpolar α phase to electroactive γ phase upon salt addition that suggests the ion‐dipole interaction between the salt and the matrix. Further, Pluronic not only hinders the PVDF crystallization that increases the amorphous character of the matrix but also interacts with the salt and hence assists in salt dissociation in the blend matrix. The dc conductivity of PVDF‐HFP/Pluronic/LiClO4 blend SPE improves with increasing the Pluronic content reaching 0.73 × 10−6 Scm−1 at room temperature with 60 wt.% Pluronic. The dispersion of GO in the same blend SPE leads to a significant jump in room temperature ion conductivity (≈1.2 × 10−6 Scm−1) with 0.4% GO. Temperature‐dependent ion conductivity of the NSPEs reveals an Arrhenius type thermally activated process. The dc polarization data indicates that the conductivity is predominantly due to ions. Impedance plots exhibit a distorted semicircle at higher frequency and a tilted spike at lower frequency. The spike is an indication of ion diffusion and electrode polarization effect. Further, GO also has enhanced the mechanical properties of the fabricated NSPEs.

Synthesis, characterization, electrical, and magnetic properties of polyvinyl alcohol/carboxymethyl cellulose blend doped with nickel ferrites nanoparticles for magneto‐electronic devices

AbstractSolid polymer electrolytes are an intriguing technology in terms of magneto‐opto electronic applications due to having a high dielectric constant, a small band gap, and excellent magnetic characteristics. In order to improve structural, optical, dielectric, conductivity, and magnetic characteristics, this research seeks to prepare nickel ferrite (NiFe2O4) nanoparticles and polyvinylalcohol (PVA)/carboxymethyl cellulose (CMC) films containing NiFe2O4. Nanoparticles of NiFe2O4 are prepared using the co‐precipitation method. The CMC/PVA–NiFe2O4 nanocomposites films are prepared using casting solution. To improve their structural, optical, conductivity, dielectric, and magnetic characteristics, these films electrolytes were examined using XRD, TEM, FT‐IR, UV–vis, and VSM measurements. According to the XRD analysis, the CMC/PVA blend polymer matrix demonstrates a considerable increase in amorphous nature with the NiFe2O4 nanoparticles (NPs) content, producing a highly flexible polymer backbone, increasing ionic conductivity of the CMC/PVA–NiFe2O4 nanocomposite films. The complexation of dopant cations with the CMC/PVA polymer matrix's backbone is confirmed by the FT‐IR spectroscopy. According to the UV–visible technique, the dopant NiFe2O4 concentration considerably affects the optical energy band gap, and Urbach energy of the pure CMC/PVA. At higher loading, these effects are more pronounced. At room temperature, ac conductivity, the dielectric behavior, and electrical modulus formalism were studied. The blend's highest AC conductivity is 4.77 × 103 S/cm. After increasing the loading of NiFe2O4 to 1.5 wt%, it increased to 8.07 × 104 S/cm. There has also been research on dielectric permittivity and electric modulus to further understand conductivity relaxation and charge storage qualities. The polymer nanocomposite, generally, displayed better optical, dielectric constant, conductivity, and magnetic characteristics compared to pure CMC/PVA being useable in terms of high energy storage nanoelectronics' manufacturing.Highlights NiFe2O4 nanoparticles were prepared by using the co‐precipitation method. Nanocomposite films of CMC/PVA–NiFe2O4 were successfully prepared by casting method. XRD patterns confirmed the increase in the degree amorphousity for nanocomposites films compare pure blend. From optical energy gap results for samples prepared was enhanced after addition NiFe2O4. The dielectric and magnetic properties showed that all nanocomposites films exhibited enhanced as compared to pure CMC/PVA film.

P3HT-Based Semi-Conductive Electrospun Nanocomposite Fibrous Emitters Doped with CsPbBr3 Perovskite Quantum Dots

Poly(3-hexylthiophene-2,5-diyl) (P3HT)-based semiconducting electrospun nanocomposite fibrous emitters were successfully fabricated by combining P3HT with poly(ethylene oxide) (PEO) and commercially available CsPbBr3 perovskite quantum dots (PQDs). The latter were employed as a synergistic photoluminescence emitter of high efficiency within the P3HT/PEO blended polymer matrix, while PEO was used as an auxiliary polymer to assist the electrospinnability of P3HT. The produced materials were characterized with respect to their chemical composition and morphology by scanning electron microscopy (SEM) and transmission electron microscopy/energy-dispersive x-ray analysis (TEM/EDX) whereas fluorescence microscopy and spectroscopy were employed to study their optical properties. Based on the obtained results, it was confirmed that the PQDs were successfully encapsulated within the electrospun fibers at a high percentage (10 wt.%), retaining at the same time their optical properties and nanoscale dimensions. Moreover, the experimental data obtained suggested the existence of inter-material interactions between P3HT and PQDs. Consequently, this study creates new pathways in the development of innovative fibrous nanocomposites with unique optoelectronic features, rendering them highly interesting in light-harvesting, sensing and optoelectronic applications.Graphic

Designing PMMA–PVA–TiO2 as New Hybrid Nanocomposite for Anticancer Applications

In this investigation, the nanocomposites were synthesized using the physical mixing technique. This technique involved adding 20% titanium dioxide (TiO2) to a combination of PMMA and PVA in terms of weight percentages. The physical properties of prepared nanocomposite have been examined by using scanning electron microscope, X-ray diffraction technique XRD, Fourier transformed infrared spectrometry (FTIR) and UV–Vis spectroscopy. XRD patterns specified that the prepared composite was mostly crystalline in nature. Scanning electron micrograph showed that TiO2 nanoparticles were covered with a polymer blend matrix. FTIR results confirmed the presence of PVA and PMMA groups on the surface of TiO2 NPs. The MTT assay method was utilized on the MSF-7 cell line in order to evaluate the potential anticancer properties of the produced components. The nanocomposites showed good activity on cancer cells.

Development of Chitosan-Copovidone nanocomposite films with antioxidant and antibacterial properties for food packaging applications

In this study, green synthesized silver nanoparticles (AgNPs) functionalized Chitosan/ Copovidone nanocomposite films were prepared by solvent casting method using glycerol as plasticizer. The AgNPs were synthesized by in-situ reduction with the aid of Syzygium cumini (SC) leaf extract, as a reducing agent of the precursor AgNO3. The main focus of this study was to examine the consequences of varying concentrations of AgNPs on the polymer blend matrix. The nanocomposite films obtained exhibited obstruction to UV light, with good transparency. The UV blocking effect of AgNPs was also computed. The developed nanocomposite films were subjected to various studies such as XRD, FTIR, Mechanical testing, SEM, hydration properties and biological activities. The outcomes indicated that the films were semi-crystalline in nature and there was effective interaction between the film components. Mechanical strength was found to improve with increasing concentration of AgNPs and the morphological images showed absence of cracks and pores. The fabricated nanocomposite films were hydrophobic in nature with lower solubility in water. They also possessed good antibacterial activity against food pathogens such as E. coli and S. aureus. The developed nanocomposite films have also exhibited retarding oxidation potential that could make it a prospective material for packaging applications especially with respect to food.