Synthesis of Zeolites from Coal Fly Ash and Their Environmental Application

This study aims to make adsorption-capable zeolite from coal fly ash, a waste product from coal-fired power plants (CFA). When it comes to commercializing sorbent, the total cost and efficiency of the adsorbent material are critical. This work used tap water instead of distilled water (DW) to synthesis zeolite from fly ashes at 90°C crystallization temperatures. The discovery lays the door for a cost-effective but easy technique of synthesizing viable zeolitic materials for adsorption applications using waste products like coal fly ash. According to the comprehensive characterization, the support for the use of TP to make zeolites is based on its larger particle size, and lower carbon impurities. The generated zeolite was homogenous and A-type, and applied as an adsorbent to remove traces of heavy metals contaminants. During a 25-minute agitation period, the zeolites produced with TP had a greater adsorption capacity. In principle, the proposed approach permits the synthesis of low-cost, high-efficiency zeolite-based adsorbent materials for environmental remediation without the use of harmful or expensive chemicals

Catalytic Reductive Degradation of Methyl Orange Using Air Resilient Copper Nanostructures

The study describes the application of oxidation resistant copper nanostructures as an efficient heterogeneous catalyst for the treatment of organic dye containing waste waters. Copper nanostructures were synthesized in an aqueous environment using modified surfactant assisted chemical reduction route. The synthesized nanostructures have been characterized by UV-Vis, Fourier transform infrared spectroscopy FTIR spectroscopy, Atomic force microscopy (AFM), Scanning Electron Microscopy (SEM), and X-ray diffractometry (XRD). These surfactant capped Cu nanostructures have been used as a heterogeneous catalyst for the comparative reductive degradation of methyl orange (MO) in the presence of sodium borohydride (NaBH4) used as a potential reductant. Copper nanoparticles (Cu NPs) were found to be more efficient compared to copper nanorods (Cu NRds) with the degradation reaction obeying pseudofirst order reaction kinetics. Shape dependent catalytic efficiency was further evaluated from activation energy (EA) of reductive degradation reaction. The more efficient Cu NPs were further employed for reductive degradation of real waste water samples containing dyes collected from the drain of different local textile industries situated in Hyderabad region, Pakistan

The in situ growth of CuO nanostructures on an ITO substrate and its application as a highly sensitive electrode for the electrochemical determination of N-acetyl-L-cysteine

This study describes the development of a new ITO-based electrode used for the electrochemical determination of N-acetyl-L-cysteine (NAC). The electrode system relies on in situ grown CuO nanostructures over the ITO substrate, which provide a relatively greater contact and enables effective electron facilitation during the electrocatalytic oxidation of NAC in an aqueous medium. In situ growth of the CuO nanostructures was achieved using a simple hydrothermal process with the application of succinic acid as an effective growth template. The grown layer of CuO possessed a dense population of highly ordered nanostructures with a high degree of structural uniformity. The study evaluates the potential of the newly developed ITO-based electrode against the bare GCE and an electrode modified via the direct deposition of the same CuO nanostructures synthesised under similar hydrothermal conditions. The electrochemical oxidation of NAC over the newly developed electrode demonstrated low-over potential value and good working linearity in the range from 0.01 to 0.28 mu M. The electrode system was found to be sensitive up to 1.2 x 10(-3) mu M (S/N = 3) with charge transfer co-efficient (alpha) and diffusion co-efficient (D) values of 0.65 and 1.62 x 10(-2) cm(2) s(-1), respectively. Moreover, the developed electrode system demonstrated excellent working capability when utilised for the determination of NAC from a pharmaceutical formulation obtained from a local pharmacy

Facile Synthesis of Polyacrylic Acid/Graphene Oxide Composite Hydrogel Electrolyte for High-Performance Flexible Supercapacitors

The development of hydrogel electrolytes plays a critical role in high-performance flexible supercapacitor devices. Herein, a composite hydrogel electrolyte of polyacrylic acid (PAA) and graphene oxide (GO) has been successfully prepared, where the oxygen-containing functional groups of GO may crosslink and form hydrogen bonds with carboxyl on the molecular chain of PAA, thereby significantly enhancing the mechanical properties of a PAA-based gel electrolyte. The tensile strength increases from 4.0 MPa for pristine PAA gel to 6.1 MPa for PAA/GO composite gel, with the elongation at break rising from 1556% to 1950%. Meanwhile, GO promotes the transportation of electrolyte ions, which are favorable for enhancing the ionic conductivity of the PAA hydrogel. As a result, the assembled supercapacitor based on PAA/GO composite hydrogel electrolyte shows enhanced capacitance retention of 64.3% at a large current density of 20 A g−1 and excellent cycling stability over 10,000 cycles at 5 A g−1. Furthermore, the fabricated flexible supercapacitor devices could maintain outstanding electrochemical performance at various bending angles of 0–90°, indicating a promising prospect for the PAA/GO hydrogel electrolyte in flexible wearable fields

Highly sensitive electrochemical determination of captopril using CuO modified ITO electrode: the effect of in situ grown nanostructures over signal sensitivity

The study describes a new approach for the direct electro-oxidation of captopril (CAP) drug using a CuO modified ITO electrode. The modified ITO electrode consists of an in situ grown film which accommodates dense CuO nanostructures with morphological features similar to flowers. The in situ growth over the ITO substrate was achieved using a simple hydrothermal route with the assistance of malonic acid which acted as an effective growth template. The devised electrode was evaluated in reference to its slurry-derived counterpart which involved surface modification of GCE using a conventional approach (drop-casting). The competitive evaluation of the discussed electrodes against the electro-oxidation of CAP, provided significant evidence to support the importance of controlled nanostructure distribution over the electrode surface to achieve higher signal sensitivity and reproducibility. The devised ITO/CuO electrode was known to possess excellent sensing capability against CAP within the linear working range of 0.01 to 3.43 mu M with signal sensitivity down to 2 x 10(-3) mM. Moreover, the ITO/CuO was noted to exhibit high charge transfer co-efficient (a), diffusion coefficient (D) and rate constant values of 0.83, 9.28 x 10(-5) cm(2) s(-1) and 3.5 x 10(3) mol(-1) L s(-1) respectively. In addition, the successful usage of ITO/CuO for CAP determination from commercial tablets and human urine samples further indicated the practical workability of the proposed electrode system

Construction of chitosan-supported nickel cobaltite composite for efficient electrochemical capacitor and water-splitting applications

Abstract The construction of highly efficient electrode material is of considerable interest, particularly for high capacitance and water-splitting applications. Herein, we present the preparation of a NiCo2O4-Chitosan (NC@Chit) nanocomposite using a simple hydrothermal technique designed for applications in high capacitance and water-splitting. The structure/composition of the NC@Chit composite was characterized using different analytical methods, containing electron microscope (SEM and TEM), and powder X-ray diffraction (XRD). When configured as an anode material, the NC@Chit displayed a high capacitance of 234 and 345 F g−1 (@1Ag−1 for GC/NC and NC@Chit, respectively) in an alkaline electrolyte. The direct use of the catalyst in electrocatalytic water-splitting i.e., HER and OER achieved an overpotential of 240 mV and 310 mV at a current density of 10 mA cm−2, respectively. The obtained Tafel slopes for OER and HER were 62 and 71 mV dec−1, respectively whereas the stability and durability of the fabricated electrodes were assessed through prolonged chronoamperometry measurement at constant for 10 h. The electrochemical water splitting was studied for modified nickel cobaltite surface using an impedance tool, and the charge transfer resistances were utilized to estimate the electrode activity

In-situ engineered MXene-TiO2/BiVO4 hybrid as an efficient photoelectrochemical platform for sensitive detection of soluble CD44 proteins

Interfacial charge-carrier recombination is a bottle-neck issue restricting photoelectrochemical biosensors advancement in the wearable clinical electronics. In this study, we propose a simple approach to construct a highly efficient photoactive heterojunction capable of functioning as an active substrate in PEC biosensing of CD44 proteins. Taking the advantage of high photocatalytic activity of BiVO4, and biocompatible yet conductive 2D-Ti3C2Tx nanosheets, a workable heterojunction was constructed between in-situ formed TiO2 from the partially oxidized Ti3C2Tx and lysine functionalized BiVO4 (TiO2/MX-BiVO4). The interfacial arrangement was ideal for promoting fast charge transfer from photo-excited BiVO4 and TiO2 to Ti3C2Tx, constructing an energy level-cascade that permits minimal charge-carrier recombination besides robust photocatalytic redox activity. The PEC biosensor relies on the ligand-protein interaction, where hyaluronic acid was directly immobilized over TiO2/MX-BiVO4 based on the interactions between carboxyl of lysine and amino moieties of hyaluronic acid. The PEC biosensor response depends on the inhibition in the measured photo-oxidation current of mediator species, i. e., ascorbic acid after the addition of CD44 proteins. The superior photo-activity, and robust heterojunction arrangement, produced a sensitive signal capable of recognizing CD44 in the wide concentration window of 2.2 x 10(-4) ng mL(-1) to 3.2 ng niL(-1) with a low-detection limit of 1.4 x 10(-2) pg mL(-1). The strong interaction between lysine functionalized BiVO4 and hyaluronic acid enabled biosensor to exhibit robust antifouling characteristics towards similar proteins such as PSA and NSE. The quantification of CD44 protein from real-blood serum samples further confirmed the biosensor's reliability for clinical application

Tartaric acid assisted in-situ growth of CuO nanostructures over ITO substrate for the electrocatalytic detection of Sudan I

The study explores the potential of newly developed ITO based electrode for the electro-catalytic detection of Sudan I. The ITO based electrode utilizes a dense layer of 2D CuO nanostructures as an effective electron-transfer facilitator which promotes the electro-catalytic sensing of Sudan I in aqueous solution. The in-situ growth of CuO nanostructures was achieved using simple hydrothermal route with the assistance of tartaric acid utilized as an effective template. The in-situ grown layer comprises of 2D CuO nanostructures with morphological features similar to flowers composed of sharp-flake like features. The electro-catalytic oxidation of Sudan I over the described electrode system demonstrated low-over potential value and excellent working stability with good analytical linearity in the range of 0.001-1.56 mu M. The ITO based electrode was found highly selective and sensitive towards Sudan I with limit of detection determined to be 1.2 x 10(-4) mu M (S/N = 3)