A carbon nanotubes modified silver electrode (CNTs-Ag) was prepared via catalytic chemical vapor deposition and characterized. The morphology, crystallinity, elemental composition, and other quality parameters of the prepared electrode were investigated using scanning electron microscopy (SEM), transmission electron microscopy (TEM), X-ray diffraction (XRD), X-ray photoelectron spectroscopy (XPS), and Raman techniques. The characterization results revealed the modification of the silver metal surface with CNTs of good characteristics. A sequential injection analysis (SIA) system was developed for studying the reaction of ascorbic acid with KIO₃ using the prepared CNTs-Ag electrode. Electrodes were polarized with both direct current (DC) and periodic square wave (SW). Various experimental conditions affecting the differential electrolytic potentiometric (DEP) peak such as current density, SW bias value, and flow rate were appraised. Under the optimum conditions, good linear responses for ascorbic acid were obtained in the range of 60.0–850.0 µM for both types of polarization with detection limits of 14.0–19.0 µM. The results obtained showed that the periodic polarization method was more sensitive than DC polarization and the electrode response was faster. Ascorbic acid in pharmaceutical tablets was determined with satisfactory results using this method. The prepared CNTs-based electrode exhibited good performance for a long period of use. The method is simple, rapid, and inexpensive for routine analysis.

This study investigates the synthesis process and characterization methods and evaluates the inhibition behavior of olanzapine (2-methyl-4-(4-methyl-1-piperazinyl)-10H-thieno-[2,3-b] 1,5]benzodiazepine (OLZ)) and its derivatives, such as 3-(2-methyl-4-(4-methylpiperazin-1-yl)-10H-benzo[b]thieno[2,3-e] [1,4]diazepin-10-yl) propenamide (OLZ1) and Ethyl 2-(2-methyl-4-(4-methylpiperazin-1-yl)-10H-benzo[b]thieno[2,3-e][1,4]diazepin-10 yl) acetate (OLZ2) for carbon steel (C1018) in a 1 M HCl acidic solution. Fourier Transform Infrared Spectroscopy (FTIR) and Nuclear Magnetic Resonance (NMR) were employed to verify their molecular structures and functional groups, which characterized the derivatives after synthesis. Their corrosion inhibition potential for C1018 steel in acidic media was estimated by weight loss (WL) and electrochemical techniques, such as electrochemical impedance spectroscopy (EIS), linear polarization resistance (LPR), and potentiodynamic polarization (PDP), accompanied by surface analysis methods. The findings revealed that all three derivatives demonstrated exceptional inhibition performance, achieving maximum efficiencies of 88.83%, 91.20%, and 91.82% for OLZ, OLZ1, and OLZ2 at 300 ppm, respectively. Weight loss experiments across different temperatures further explored their inhibitory behavior. Although inhibition efficiency decreased with a temperature increase to 318 K, the derivatives still displayed notable performance, with maximum efficiencies of 74.75% for OLZ, 81.63% for OLZ1, and 79.44% for OLZ2. Polarization studies identified the corrosion inhibition mechanisms as an anodic type. Surface characterization of the C1018 steel coupons, both with and without the inhibitors, was performed using FTIR and scanning electron microscopy (SEM) combined with energy-dispersive X-ray spectroscopy (EDX). These analyses indicated the creation of a protective inhibitor layer on the carbon steel surface, reducing corrosion in the acidic environment. Overall, this study underscores the potential of these drug derivatives as corrosion inhibitors, combining structural insights and performance assessments to support their industrial application.

This study investigates the synthesis process, characterization methods and evaluates the inhibition behavior of Olanzapine derivatives (OLZ, OLZ1, and OLZ2) for carbon steel (C1018) in a 1 M HCl acidic solution. Fourier Transform Infrared Spectroscopy (FTIR) and Nuclear Magnetic Resonance (NMR) to verify their molecular structures and functional groups, which characterized the derivatives after synthesis. Their corrosion inhibition potential for C1018 steel in acidic media was estimated by weight-loss (WL) and electrochemical techniques (EIS, LPR, and PDP), accompanied by surface analysis methods. The findings revealed that all three derivatives demonstrated exceptional inhibition performance, achieving maximum efficiencies of 88.83%, 91.20%, and 91.82% for OLZ, OLZ1, and OLZ2 at 300 ppm, respectively. Weight-loss experiments across different temperatures further explored their inhibitory behavior. Although inhibition efficiency decreased with a temperature increase to 318 K, the derivatives still displayed notable performance, with maximum efficiencies of 74.75% for OLZ, 81.63% for OLZ1, and 79.44% for OLZ2. Polarization studies identified the corrosion inhibition mechanisms as anodic type. Surface characterization of the C1018 steel coupons, both with and without the inhibitors, was performed using FTIR, scanning electron microscopy (SEM), combined with energy-dispersive X-ray spectroscopy (EDX). These analyses indicated the creation of a protective inhibitor layer on the carbon steel surface, reducing corrosion in the acidic environment. Overall, the study underscores the potential of these drug derivatives as green corrosion inhibitors, combining structural insights and performance assessments to support their industrial application.