Development of quinoline-based heteroatom polybenzoxazines reinforced graphitic carbon nitride (GCN) carbonisation composites for emerging supercapacitor applications.

The current research described in this paper, focuses on the development of a new quinoline-based Mannich-type benzoxazine and its use to obtain advanced carbonisation materials with a high energy storage capacity. Based on this, a quinoline-based benzoxazine monomer (Q-xda) was synthesised by a reaction between 8-hydroxyquinoline, xylylenediamine and paraformaldehyde, and it is characterised by FT-IR and 1H-NMR spectroscopy. Composites were prepared from the benzoxazine and variable weight percentages of graphitic carbon nitride (GCN) (i.e., 5, 10, and 15 wt%). The oxazine ring-opening curing process of the polybenzoxazine composites, and its subsequent pyrolysis reaction was performed; and their chemical structures were confirmed using FT-IR spectroscopy. Also, the thermal and morphological characteristics of the composites were evaluated by XRD, thermogravimetric analysis (TGA), and SEM analyses. According to the results of the thermal experiments, adding GCN reinforcement significantly increased the thermal stability and char yield of the resultant composites. Electrochemical, and hydrophobic investigations were also carried out, and the results of these suggesting that the composites reinforced with 15 wt% GCN exhibit the highest dielectric constant (high κ = 10.2) and contact angle (145°). However, all the crosslinked composites demonstrated a remarkable electrochemical performance as pseudocapacitors. The resulting poly(Q-xda) + 15 wt% GCN electrodes showed a higher capacitance and a lower transferred charge resistance (i.e., 370 F g-1 at 6 A g-1 and 20.8 Ω) than the poly(Q-xda) electrode (i.e., 216 F g-1 at 6 A g-1 and 26.0 Ω). In addition, the poly(Q-xda) + 15% GCN exhibited a cycling efficiency of 96.2% even after 2000 cycles. From these results, it can be concluded that the constructed electrodes perform well in electrochemical operations.

Sulfonated Poly Ether Sulfone Membrane Reinforced with Bismuth-Based Organic and Inorganic Additives for Fuel Cells.

This research work focuses on developing a robust polymer electrolyte membrane (PEM) with high proton efficiency toward proton exchange membrane fuel cells (PEMFCs). In this study, poly ether sulfone (PES) was sulfonated by chlorosulfonic acid to yield sulfonated poly ether sulfone (SPES) followed by incorporation with bismuth-based additives such as bismuth trimesic acid (BiTMA) and bismuth molybdenum oxide (Bi2MoO6). The composite membrane was thoroughly investigated for its structural and physicochemical properties such as FT-IR, SEM, TGA, contact angle, water uptake, oxidative stability, ion-exchange capacity, and swelling ratio. Incorporation of additives into the polymer was confirmed by XPS and XRD analysis. The proton conductance of the pristine SPES is 4.19 × 10-3 S cm-1, whereas that of the composite membrane SPES/BiTMA-10 is 10 × 10-3 S cm-1 and that of SPES/Bi2MoO6-15 is 7.314 × 10-3 S cm-1; both the composite membranes exhibit higher proton conductivity than the pristine SPES membrane. The physicochemical characteristics and impedance measurements of the electrolyte reported can be viable to the PEM membrane.

Supercapacitor and high k properties of CNT-PbS reinforced quinoxaline amine based polybenzoxazine composites.

The new 2,3-diphenylquinoxalin-6-amine (dpqa) was designed and synthesized through an efficient and high yield condensation process. Data from FTIR and 1H-NMR spectroscopy have been adopted to ascertain the molecular structure of benzoxazine compounds. Furthermore, the quinoxaline amine based benzoxazine (BA-dpqa) was synthesized using bisphenol-A and paraformaldehyde followed by combining different weight percentages (1, 5 and 10 wt%) of (3-glycidyloxypropyl)trimethoxysilane functionalized CNT-PbS with benzoxazine to obtain nanocomposites. The thermal and morphological properties of the quinoxaline amine based neat polybenzoxazine matrix poly(BA-dpqa) and CNT-PbS/poly(BA-dpqa) composites were analysed by XRD, TGA and SEM analysis. The values of the degradation temperature (Td) obtained for neat poly(BA-dpqa) and 10 wt% CNT-PbS/poly(BA-dpqa) composites are 414 °C and 424 °C. Furthermore, the chair yield percentage was calculated as 33% and 35% respectively. The water contact angle of polybenzoxazine gradually increased from 89° to 127° proportional to the content of CNT-PbS. Among the composites, 10 wt% CNT-PbS reinforced poly(BA-dpqa) nanocomposites possess higher dielectric constant (k = 11.0) than other composites. The pseudocapacitor nature of the prepared electrodes is demonstrated by the good electrochemical performance according to the CV curve. Also, the prepared 10 wt% CNT-PbS/poly(BA-dpqa) (637 F g-1 at 5 A g-1 and 11.8 Ω) electrode shows better capacitance and lower charge transfer resistance values than 5 wt% CNT-PbS/poly(BA-dpqa) (613 F g-1 at 5 A g-1 and 13.2 Ω) and neat poly(BA-dpqa) (105 F g-1 at 5 A g-1 and 15.6 Ω) according to the charge/discharge curves and EIS spectra. 10 wt% CNT-PbS/poly(BA-dpqa) shows 99.2% cycling efficiency even at the 2000th cycle, which indicates the good electrochemical performance of the prepared electrode.

Electrochemical sensing of copper (II) ion in water using bi-metal oxide framework modified glassy carbon electrode.

In this research, an electrochemical sensor was fabricated employing the metal-organic framework (MOF) deposited glassy carbon electrode (GCE) for the sensing copper ions in water with high sensitivity. The porous nanostructured MOF was characterized through Transmission electron microscope, scanning electron microscope and X-ray diffraction analysis. The Bi-MOF nanostructure deposited GCE (Bi-MOF/GCE) was fabricated by drop-casting a suspension of Bi-MOF in water on GCE surface. The performance of modified electrode in the presence and absence of heavy metal ions such as Cd2+, Hg2+ As3+, Pb2+ and Cu2+ was determined by the cyclic voltammetry in deionised water within the scan rate range of 25 and 300 mVs-1. The Bi-MOF/GCE displayed highest anodic and cathodic peak current for Cu2+ ions than other metal ions, which was enhanced linearly within the scan rate range of 10-100 mV s-1. Under the employed experimental conditions, the fabricated Bi-MOF/GCE based electrochemical sensor showed an outstanding routine in the determination of copper with a lowest sensing limit of 1 × 10-5 M, wide linear range variation, strong interaction between metal ions and Bi-MOF. It has long-term stability and good reproducibility. The Bi-MOF/GCE electrode was successfully tested to detect Cu2+ in tap water with acceptable results.

Dual labeled Ag@SiO2 core-shell nanoparticle based optical immunosensor for sensitive detection of E. coli.

An optical nanobiosensor is presented using a fluorescent dye and anti-E. coli McAb anchored Ag@Silica core shell nanoparticles, for rapid and sensitive Escherichia coli detection in environmental samples. The synthesized dual labeled core shell (DLCS) nanoparticle shows intense fluorescence at 620 nm in solution, having a narrow emission with full width at half maxima (FWHM) of 10 nm, as a prerequisite to develop a sensitive detection platform for various biosensing applications. The specific E. coli was captured using an anti-E. coli antibody functionalized quartz glass, followed by a treatment with DLCS, where the photoluminescence spectroscopy was used to detect the target pathogen. The fabrication of the quartz glass based optical-immunosensor was monitored, and the results show changes in the photoluminescent patterns, which substantiate that varied species were immobilized on the surface of the antibody modified quartz glass. Consequently, the optical immunosensor demonstrated specificity and improved sensitivity, as compared to the customary methods, and was able to detect as low as 5CFU/mL. The developed DLCS based optical immunosensor was evaluated with environmental water samples, which showed acceptable precision, reproducibility and stability, and could be readily applied to the routine monitoring of pathogenic microorganisms in the environmental samples, and most importantly, demonstrate the potential of a prototype development of a simple and inexpensive diagnostic technique.

pH-Dependent encapsulation of pyrene in PPI-core:PAMAM-shell dendrimers.

Core-shell dendrimers consisting of poly(propyleneimine) (PPI) dendrimer as a core and poly(amidoamine) (PAMAM) dendrons as a shell have been synthesized through the route of Michael addition reaction followed by amidation. These macromolecules were investigated their ability to solubilize a guest molecule, pyrene. The number of encapsulated pyrene molecules per dendrimer increased with pH of a solution and generation (G) of PAMAM dendron, and it reached 2.7 for PPI(G3)-core:PAMAM(G3)-shell dendrimer at pH 11. It was confirmed that the solubilized pyrene located in the hydrophobic nanocavities of the PPI dendrimer core in the dendrimer. The shrunk PAMAM dendron shell should play a role of retention fence of doped molecules.