The increased interest in the transition from liquid to solid polymer electrolytes (SPEs) has driven enormous research in the area polymer electrolyte technology. Solid biopolymer electrolytes (SBEs) are a special class of SPEs that are obtained from natural polymers. Recently, SBEs have been generating much attention because they are simple, inexpensive, and environmentally friendly. In this work, SBEs based on glycerol-plasticized methylcellulose/pectin/potassium phosphate (MC/PC/K₃PO₄) are investigated for their potential application in an electrochemical double-layer capacitor (EDLC). The structural, electrical, thermal, dielectric, and energy moduli of the SBEs were analyzed via X-ray diffractometry (XRD), Fourier transforms infrared spectroscopy (FTIR), electrochemical impedance spectroscopy (EIS), transference number measurement (TNM), and linear sweep voltammetry (LSV). The plasticizing effect of glycerol in the MC/PC/K₃PO₄/glycerol system was confirmed by the change in the intensity of the samples’ FTIR absorption bands. The broadening of the XRD peaks demonstrates that the amorphous component of SBEs increases with increasing glycerol concentration, while EIS plots demonstrate an increase in ionic conductivity with increasing plasticizer content owing to the formation of charge-transfer complexes and the expansion of amorphous domains in polymer electrolytes (PEs). The sample containing 50% glycerol has a maximal ionic conductivity of about 7.5 × 10⁻⁴ scm⁻¹, a broad potential window of 3.99 V, and a cation transference number of 0.959 at room temperature. Using the cyclic voltammetry (CV) test, the EDLC constructed from the sample with the highest conductivity revealed a capacitive characteristic. At 5 mVs⁻¹, a leaf-shaped profile with a specific capacitance of 57.14 Fg⁻¹ was measured based on the CV data.

Magnetite (Fe₃O₄) have been thoroughly investigated as microwave absorbing material due to its excellent electromagnetic properties (permittivity and permeability) and favorable saturation magnetization. However, large density and impedance mismatch are some of the limiting factors that hinder its microwave absorption performance (MAP). Herein, Fe₃O₄ nanoparticles prepared by facile co-precipitation method have been coated with citric acid and embedded in a polyvinylidene fluoride (PVDF) matrix. The coated Fe₃O₄ nanoparticles were characterized by X-ray diffraction spectrometer (XRD), field emission scanning electron microscopy (FESEM), Fourier transform infrared spectroscopy (FTIR), and vibrating sample magnetometer (VSM). COMSOL Multiphysics based on the finite element method was used to simulate the rectangular waveguide at X-band and Ku-band frequency range in three-dimensional geometry. The citric acid coated Fe₃O₄/PVDF composite with 40 wt.% filler loading displayed good microwave absorption ability over the studied frequency range (8.2–18 GHz). A minimum reflection loss of −47.3 dB occurs at 17.9 GHz with 2.5 mm absorber thickness. The composite of citric acid coated Fe₃O₄ and PVDF was thus verified as a potential absorptive material with improved MAP. These enhanced absorption coefficients can be ascribed to favorable impedance match and moderate attenuation.

In this research, nanocomposite solid polymer electrolytes (NCSPEs) comprising methylcellulose/pectin (MC/PC) blend as host polymer, ammonium chloride (NH₄Cl) as an ion source, and zinc oxide nanoparticles (ZnO NPs) as nanofillers were synthesized via a solution cast methodology. Techniques such as Fourier transform infrared (FTIR), electrical impedance spectroscopy (EIS), and linear sweep voltammetry (LSV) were employed to characterize the electrolyte. FTIR confirmed that the polymers, NH₄Cl salt, and ZnO nanofiller interact with one another appreciably. EIS demonstrated the feasibility of achieving a conductivity of 3.13 × 10⁻⁴ Scm⁻¹ for the optimum electrolyte at room temperature. Using the dielectric formalism technique, the dielectric properties, energy modulus, and relaxation time of NH₄Cl in MC/PC/NH₄Cl and MC/PC/NH₄Cl/ZnO systems were determined. The contribution of chain dynamics and ion mobility was acknowledged by the presence of a peak in the imaginary portion of the modulus study. The LSV measurement yielded 4.55 V for the comparatively highest conductivity NCSPE.

Due to the geographical location and technological limitation, various novel enhanced oil recovery (EOR) methods has been proposed to recover the remaining oil from a depleted oil reservoir. Research on application of nanoparticles either on its own or coupled with other stimulating agents has been growing enormously and some of them have shown a promising future. In high temperature and high pressure reservoirs, thermal degradation will cause failure to the conventional chemicals. In this work, temperature-stable YIG magnetic nanoparticles with an electromagnetic wave has been proposed as a new candidate for reservoir stimulating agent. The purpose of nanoparticle injection is to increase the sweep efficiency in the reservoir by increasing the viscosity of displacing fluid. In this research, Yttrium iron garnet (YIG) nanoparticles have been injected into a waterflooded oil saturated porous medium to recover the remaining oil in the presence of an electromagnetic wave. At the sintering temperature 1200°C, a mixture of hematite and YIG was obtained, suggesting a higher temperature for single phase YIG. From VSM analysis, the average magnetic saturation, coercivity and remanence are 18.17 emu/g, 21.73 Oe and 2.38 emu/g, respectively. 1.0 wt% of YIG nanofluid was prepared and subsequently injected into the pre-saturated porous medium in the presence of square electromagnetic wave of 13.6 MHz. As much as 43.64% of the remaining oil in place (ROIP) was recovered following the injection of 2 pore volume of YIG nanofluid.

Presence of GO in PU muffles discharge of heat, smoke and CO and CO2 into atmosphere. The maximum improvement in mechanical properties achieved by including 2.0 wt-% of GO in PU framework, indicating an increase in tensile stress and elongation at break of 155.1% and 27.7% compared to PU. Primary temperature of thermal degradation of PU/GO nanocomposite increased by 36.5°C with 3.0 wt-% of GO. Charred yield of PU/GO composites augmented due to GOs’ physical hindrance which limits diffusion of flammable gas. Muffling effect of GO in danger of flame and smoke exposure of polymer composites decreased by introduction of 3.0 wt-% of GO. Uniform distribution of GOs within PU matrix formed a strong, twisted route and sticky char in PU/GO composites and delayed thermal deterioration process. Thereby, this work introduces an important method for improving thermal stability and fire protection of PU providing an effective application for coating industry.