Corrosion inhibitors represent one of the most commonly used methods for significantly reducing the corrosion rate of metals and alloys. Adsorption inhibitors have a wide range of applications in cooling water systems, deicing solutions for aircrafts, airports and ways, etching and degreasing solutions, oil pipelines, paints and coatings and metal processing solutions. Adsorption corrosion inhibitors of metals and alloys are generally organic compounds that contain structures with heteroatoms (N, P, S, As, O) in their molecules, having lone pair electrons or π electrons in aromatic rings or multiple bonds. They enable relatively strong interactions between the metal atoms and organic molecules, resulting in a protective layer of organic molecules adsorbed at the metal–corrosive solution interface. Most molecules of active substances from drugs contain similar structures, which is why many drugs have been already tested as corrosion inhibitors. One of the major disadvantages of using drugs for this purpose is their particularly high price. To overcome this impediment, the possibility of using expired drugs as corrosion inhibitors has been investigated since 2009. The present paper is an exhaustive compilation of the scientific published papers devoted to the use of expired drugs as corrosion inhibitors in various aggressive solutions. The inhibitory efficiencies of expired drugs are presented as a function of the studied metal or alloy and the nature of the aggressive solution, as well as the concentration of the inhibitor in such a solution. Research has especially been focused on mild and carbon steel and less on stainless steel, as well as on some metals such as copper, zinc, nickel, tin and aluminum and its alloys. The experimental methods used to assess the inhibitory efficiencies of expired drugs are briefly discussed. Also, the available information on the stability of the active substances in the drugs is presented, although most authors were not concerned with this aspect. Finally, several actions are revealed that must be undertaken by researchers so that the results obtained in the study of the anticorrosive action of expired drugs can be applied at the industrial level and not remain only an academic concern.

For proton exchange membrane water electrolysis (PEMWE) to become competitive, the cost of stack components, such as bipolar plates (BPP), needs to be reduced. This can be achieved by using coated low-cost materials, such as copper as alternative to titanium. Herein we report on highly corrosion-resistant copper BPP coated with niobium. All investigated samples showed excellent corrosion resistance properties, with corrosion currents lower than 0.1 µA cm⁻² in a simulated PEM electrolyzer environment at two different pH values. The physico-chemical properties of the Nb coatings are thoroughly characterized by scanning electron microscopy (SEM), electrochemical impedance spectroscopy (EIS), X-ray photoelectron spectroscopy (XPS), and atomic force microscopy (AFM). A 30 µm thick Nb coating fully protects the Cu against corrosion due to the formation of a passive oxide layer on its surface, predominantly composed of Nb₂O₅. The thickness of the passive oxide layer determined by both EIS and XPS is in the range of 10 nm. The results reported here demonstrate the effectiveness of Nb for protecting Cu against corrosion, opening the possibility to use it for the manufacturing of BPP for PEMWE. The latter was confirmed by its successful implementation in a single cell PEMWE based on hydraulic compression technology.

To enhance the sliding wear and corrosion behavior of steels with low carbon content, cermet composite coatings are usually deposited on their surface by various deposition processes. Laser cladding, compared to other deposition techniques such as electroplating, arc welding, and thermal spraying, has numerous advantages to produce such protective coatings. The paper presents the optimization of laser cladding deposition speed versus energy density in order to obtain WC-Co/NiCrBSi coatings with Ni-Al addition free of defects and reduced porosity deposited on low carbon steel substrate. The microstructure and chemical composition were investigated by SEM combined with EDX analysis while XRD was performed in order to examinate the phases within the coatings. In order to investigate the cladding speed influence on the coatings, hardness measurements, POD (pin on disk) wear tests and corrosion tests in 3.5% NaCl solution were carried out. The results showed that an optimal cladding speed has a crucial impact on the microstructure, composition, and hardness. It was found out that optimizing the cladding deposition speed proved to be effective in enhancing the sliding wear resistance and corrosion behavior by controlling the iron content within the coatings.

In this work, raspberry (Rubus idaeus) leaves were converted to powder and used as a new natural lignocellulosic low-cost adsorbent for methylene blue removal from aqueous solutions. Different techniques (FTIR, SEM, color analysis, and pH_PZC determination) were applied for adsorbent characterization. The effects of pH, ionic strength, contact time, adsorbent dose, initial deconcentration, and temperature on adsorption capacity were investigated. Equilibrium, kinetic, and thermodynamic studies have shown that the adsorption is best described by the Sips isotherm and pseudo-second-order kinetic model and that the process is spontaneous, favorable, and endothermic, involving physisorption as the main mechanism. The maximum adsorption capacity was 244.6 (mg g⁻¹) higher compared to other adsorbents based on plant leaves. The Taguchi method and the ANOVA analysis were used to optimize the adsorption conditions. The contact time was the factor with the highest influence on the process, while the temperature had the lowest influence. A desorption study was also performed to determine the possibility of adsorbent regeneration.

The performance of a new eco-friendly adsorbent, obtained from motherwort (Leonurus cardiaca L.) biomass after minimum processing, in crystal violet dye removal from aqueous solutions was studied. Firstly, the adsorbent material was characterized using several technics, such as FTIR, pH_PZC determination, SEM and color analysis. The next step was to determine the influence of initial dye concentration, contact time, temperature, pH, adsorbent dose and ionic strength on adsorbent adsorption capacity. Equilibrium, kinetic, thermodynamic, optimization and desorption studies were performed in a batch system for studying all aspects related to the adsorption process. The sips isotherm best fit the experimental data with a predicted maximum adsorption capacity of 125.6 (mg g⁻¹). The kinetic data indicate that equilibrium is reached at 50 min and that general order is the best kinetic model to describe the dye retention. The process is endothermic, spontaneous, favorable and supposed to be a physical adsorption. In addition to establishing the optimal adsorption conditions, Taguchi methods and ANOVA analysis showed that the pH is the most influencing parameter of the adsorption process, having a contribution of 61.64%. All the presented data show that the motherwort biomass powder is very suitable to be used as at low-cost, easy available and effective adsorbent for the crystal violet dye removal from aqueous solutions.