Quantum Chemical and Experimental Evaluation of a 4-Amino-Antipyrine Based Schiff Base as Corrosion Inhibitor for Steel Material.

Electrochemical experiments such as potentiodynamic polarization, electrochemical impedance spectroscopy, and gravimetric studies have been used to examine the corrosion inhibitory efficacy of 4-[(4-nitrobenzylidene)-amino]-antipyrine (4-NBAAP) on mild steel (MS) in 1 M HCl. 4-NBAAP inhibits the corrosion of MS through a mixed inhibition mechanism, according to the electrochemical investigation. The efficiency of 4-NBAAP increases with an increase in the inhibitor concentration and decreases with an increase in temperature. The adsorption of 4-NBAAP molecules on the MS surface follows the Langmuir adsorption isotherm. To find the relationship between the 4-NBAAP molecular structure and inhibitive effect, a few thermodynamic parameters were computed. The experimental results obtained from gravimetric and different electrochemical investigations prove the superiority of the inhibitor at higher concentrations in controlling the corrosion process of the steel in aggressive environments. Also, quantum chemical studies were performed to provide further insights into the inhibition mechanism.

Fabrication of Mechanically Alloyed Super Duplex Stainless Steel Powder-Modified Carbon Paste Electrode for the Determination of Methylene Blue by the Cyclic Voltammetry Technique.

Alloys with an equal balance of ferrite and austenite provide super duplex stainless steel (DSS) with enhanced strength and corrosion resistance. This study utilized mechanical alloying to produce nanostructured super duplex stainless steel powders for the identification of methylene blue dye in wastewater. High-energy particle grinding was employed to create the SAF-2507 DSS powders. To electrochemically oxidize methylene blue dye in wastewater, a modified carbon paste electrode (DSS-MCPE) was developed. Methylene blue, a water-soluble cationic colorant extensively used in the paper, pulp, and textile industries, poses a threat to human health and water supplies when improperly disposed of. DSS-MCPE demonstrated a significant current response, indicating its capability to detect methylene blue dye in a pH range of 6-8. The experiment revealed that 2 mg of DSS-MCPE produced a maximum current response of 72.22 µA, facilitating the effective electrooxidation of methylene blue dye in wastewater. Furthermore, the investigation demonstrated that the active surface area of the 2 mg of DSS-MCPE (0.478 cm2) was greater than that of the bare carbon paste electrode (BCPE) (0.054 cm2). The increased active surface area was correlated with an enhanced current response. The strong interaction between methylene blue molecules at the interface of the produced 2 mg of DSS-MCPE contributed to the observed increase in anodic current across methylene blue concentrations ranging from 0.1 to 0.6 mM.

Electrochemical Detection of Uric Acid Based on a Carbon Paste Electrode Modified with Ta2O5 Recovered from Ore by a Novel Method.

Except for well-known commercial production procedures, this study demonstrates that Ta2O5 particles can be produced. Through a series of steps, highly pure Ta2O5 particles (99.45%) were produced from the raw ore. We have electrochemically detected one of the important nitrogenous compounds present in urine, "uric acid", by a Ta2O5 particle-modified carbon paste electrode (Ta2O5-MCPE) using cyclic voltammetry. The prepared electrode has shown excellent current sensitivity at a pH of 6.0 phosphate-buffered solution. We have found that 4 mg Ta2O5-MCPE has recorded the highest current sensitivity of 75.75 µA. The oxidation peak current was varied with the uric acid concentration in the range from 1 to 5 mM at 4 mg Ta2O5-MCPE. We have calculated the electrode-active surface area for a bare carbon paste electrode and 4 mg Ta2O5-MCPE using the Randles-Sevcik equation, and the values were found to be 0.0202 and 0.0450 cm2, respectively. On the other hand, the calculated values of limit of detection and limit of quantification were reported as 0.5937 × 10-8 M and 1.9791 × 10-8 M, respectively, for the prepared 4 mg Ta2O5-MCPE. The interfere studies revealed that the variation in the electrochemical signal of uric acid in the presence of different metal ions was found to be less than ±5%.

TiO2-Decorated by Nano-γ-Fe2O3 as a Catalyst for Efficient Photocatalytic Degradation of Orange G Dye under Eco-friendly White LED Irradiation.

Azo dyes make up a major class of dyes that have been widely studied for their diverse applications. In this study, we successfully applied nano-γ-Fe2O3/TiO2 as a nanocatalyst to improve the photodegradation efficiency of azo dyes (Orange G (OG) dye as a model) from aqueous solution under white light-emitting diode (LED) irradiation. We also investigated the degradation mechanisms and pathways of OG dye as well as the effects of the initial pH value, amount of H2O2, catalyst dosage, and dye concentration on the degradation processes. The characterizations of nano-γ-Fe2O3 and γ-Fe2O3 Nps/TiO2 were carried out using various techniques, including X-ray diffractometry, scanning electron microscopy, energy-dispersive X-ray spectroscopy, Fourier transform infrared spectroscopy, and UV-visible spectroscopy. The efficiency of the photodegradation reaction of OG was found to follow pseudo-first-order kinetics (Langmuir-Hinshelwood model) with a rate constant of 0.0338 min-1 and an R2 of 0.9906. Scavenger experiments revealed that hydroxyl radicals and superoxide anion radicals were the dominant species in the OG photocatalytic oxidation mechanism. This work provides a new method for designing highly efficient heterostructure-based photocatalysts (γ-Fe2O3 Nps/TiO2) based on LED light irradiation for environmental applications.

Assessing the Food Quality Using Carbon Nanomaterial Based Electrodes by Voltammetric Techniques.

The world is facing a global financial loss and health effects due to food quality adulteration and contamination, which are seriously affecting human health. Synthetic colors, flavors, and preservatives are added to make food more attractive to consumers. Therefore, food safety has become one of the fundamental needs of mankind. Due to the importance of food safety, the world is in great need of developing desirable and accurate methods for determining the quality of food. In recent years, the electrochemical methods have become more popular, due to their simplicity, ease in handling, economics, and specificity in determining food safety. Common food contaminants, such as pesticides, additives, and animal drug residues, cause foods that are most vulnerable to contamination to undergo evaluation frequently. The present review article discusses the electrochemical detection of the above food contaminants using different carbon nanomaterials, such as carbon nanotubes (CNTs), graphene, ordered mesoporous carbon (OMC), carbon dots, boron doped diamond (BDD), and fullerenes. The voltammetric methods, such as cyclic voltammetry (CV) and differential pulse voltammetry (DPV), have been proven to be potential methods for determining food contaminants. The use of carbon-based electrodes has the added advantage of electrochemically sensing the food contaminants due to their excellent sensitivity, specificity, large surface area, high porosity, antifouling, and biocompatibility.

Synthesis and Characterization of High Entropy Alloy 23Fe-21Cr-18Ni-20Ti-18Mn for Electrochemical Sensor Applications.

High entropy alloys (HEA) are one of the modern-era alloys accelerating with greater velocity because of their excellent properties and different applications. In the present paper, we have successfully fabricated HEA (23Fe-21Cr-18Ni-20Ti-18Mn) powders by ball milling the elemental Fe, Cr, Ni, Ti, and Mn powders for 15 h. The advancement of the milling process and phase transformation of HEAs were studied by using X-ray diffraction (XRD) and scanning electron microscope (SEM). The crystallite size and the lattice strain of the HEA were calculated by using the Williamson-Hall (W-H) equation and the values were found to be 7 nm and 0.0176%, respectively. Similarly, the true lattice parameter was calculated using the Nelson-Riley (N-R) extrapolation method, and the value was found to be 3.544 Å. We have successfully investigated the electrochemical response of 15 h ball milled 23Fe-21Cr-18Ni-20Ti-18Mn HEA powders to determine the ascorbic acid (AA) using cyclic voltammetry. We have modified the carbon paste electrode with ball milled HEA of concentrations 0, 2, 4, 6, 8, and 10 mg, and among them, 8 mg HEA modified carbon paste electrode (HEA-MCPE) depicted the highest current sensitivity. We reported the effect of modifier concentration, analyte concentration, scan rate, and pH on the oxidation peak of AA. The electrochemical active surface area of carbon paste and MCPE was calculated using the Nernst equation and the values were found to be 0.0014 cm2 and 0.0027 cm2, respectively. The fabricated HEA-MCPE showed excellent current sensitivity, stability, anti-fouling, and selectivity.