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Investigating the structural, optical, and thermal behavior of CuCl2 incorporated PVP/glycerin-based polymer electrolytes for energy storage applications
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Polymer electrolyte films composed of PVP and PVP/glycerin with varying concentrations of CuCl2 (10, 20, and 30 wt.%) were synthesized using the solution casting method. The synthesized electrolyte films were characterized using FTIR, XRD, UV-Vis, DSC, and TGA techniques. FTIR spectroscopy revealed an O-H stretching vibration of PVP around 3300 cm(-1), which experienced broadening and a reduction in intensity upon the introduction of glycerin and CuCl2. XRD analysis displayed a characteristic peak at 2 theta similar to 20 degrees, with the peak shifting towards higher angles and a slight decrease in intensity as the CuCl2 concentration increased, indicating a disruption of the crystalline structure of the host matrix. UV-Vis analysis revealed that the optical bandgap of pure PVP was 3.6 eV, whereas the incorporation of 10, 20, and 30 wt.% CuCl2 into the PVP/glycerin system resulted in a significant reduction of the bandgap to 2.4, 1.7, and 1.4 eV, respectively. DSC measurements indicated a decrease in the glass transition temperature (T-g) from 150 degrees C for pure PVP to 146, 144, and 140 degrees C for the PVP/glycerin composites containing 10, 20, and 30% CuCl2, respectively. TGA results indicated enhanced thermal stability for PVP/glycerin with CuCl2, which remained stable up to 225 degrees C, compared to pure PVP. According to conductivity measurements, the highest ionic conductivity achieved for a system containing 20 wt.% CuCl2 is 6.47 x 10(-4) S/cm at room temperature. The experimental data suggest that these optimized electrolyte materials could be suitable candidates for high-performance energy storage technologies.

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Publication Date
Thu Nov 19 2020
Journal Name
Indonesian Journal Of Chemistry
Determination of Eugenol in Personal-Care Products by Dispersive Liquid-Liquid Microextraction Followed by Spectrophotometry Using <i>p</i>-Amino-<i>N,N</i>-dimethylaniline as a Derivatizing Agent
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Two simple methods for the determination of eugenol were developed. The first depends on the oxidative coupling of eugenol with p-amino-N,N-dimethylaniline (PADA) in the presence of K3[Fe(CN)6]. A linear regression calibration plot for eugenol was constructed at 600 nm, within a concentration range of 0.25-2.50 μg.mL–1 and a correlation coefficient (r) value of 0.9988. The limits of detection (LOD) and quantitation (LOQ) were 0.086 and 0.284 μg.mL–1, respectively. The second method is based on the dispersive liquid-liquid microextraction of the derivatized oxidative coupling product of eugenol with PADA. Under the optimized extraction procedure, the extracted colored product was determined spectrophotometrically at 618 nm. A l

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