Inhibition effect of horehound (Marrubium vulgare L.) extract towards C38 steel corrosion in HCl solution

The corrosion inhibition properties of horehound (Marrubium vulgare L.) extract (HE) in 1 M hydrochloric acid medium was carried out using electrochemical methods (polarization curve and electrochemical impedance spectroscopy). Experiments were performed by concentration of the inhibitor and temperature effect. The results showed variation in inhibition performance of this plant extract. The Langmuir model was tested to describe the adsorption behavior of the inhibitor on the C38 steel surface. Some thermodynamic functions of dissolution processes were also determined.     

Theoretical approach to the corrosion inhibition efficiency of some quinoxaline derivatives of steel in acid media using the DFT method

Corrosion inhibition efficiencies of 1,4-dihydroquinoxaline-2,3-dione (Q1) and 2-phenylthieno[2,3-b]quinoxaline (Q2) as corrosion inhibitors against the corrosion of steel surface in hydrochloric acid is studied by means of density functional approach B3LYP/6-31G calculations. Quantum chemical parameters such as highest occupied molecular orbital energy (E _HOMO), lowest unoccupied molecular orbital energy (E _LUMO), energy gap (ΔE), dipole moment (μ), electronegativity (χ), electron affinity (A), global hardness (η), softness (σ), ionization potential (I), the fraction of electrons transferred (?N), the global electrophilicity ω, and the total energy were calculated. All calculations have been performed by considering density functional theory using the GAUSSIAN03W suite of programs.     

Adsorption and inhibition effect of curcumin on mild steel corrosion in hydrochloric acid

The inhibition effect of curcumin on the corrosion of mild steel in 1.0 M HCl solution was studied by weight loss, potentiodynamic polarization curves and electrochemical impedance spectroscopy (EIS) methods. The experimental results suggest that this compound is an efficient corrosion inhibitor and the inhibition efficiency increases with the increase in inhibitor concentration. Adsorption of this compound on mild steel surface obeys Langmuir isotherm. Also the objective of this work is to attempt to find relationships between electronic structure and inhibition efficiency. The structural parameters, such as the frontier molecular orbital energies (E _HOMO and E _LUMO), gap of energy ΔE, from the molecule to iron as well as electronic parameters such as Mulliken atomic populations were calculated and discussed using the Density Functional Theory method (DFT).     

Use of hydroxylapatite composite membranes for analysis of bisphenol A

This study evaluates solid-phase micro-extraction (SPME) coupled with gas chromatography–mass spectrometry (GC–MS) to determine trace levels of bis-phenol A in water and leached from plastic containers. In our study, we used very thin composite membranes prepared in the laboratory. The extraction using headspace post-derivatization with bis(trimethylsilyl) trifluoroacetamide (BSTFA), containing 1 % trimethylchlorosilane (TMCS) vapor, following SPME was compared with extraction without derivatization. The SPME experimental procedures to extract bis-phenol A in water were optimized with a relatively polar polyacrylate (PA)-coated fiber, an extraction time of 50 min, and desorption at 300 °C for 2 min. Headspace derivatization following SPME was performed using 7 μL of BSTFA with 1 % TMCS at 65 °C for 30 s. The precision was 5.2 % without derivatization and 9.0 % headspace derivatization. The detection limit was determined to be at the nanogram per liter level. When SPME was used following headspace derivatization, the detection limit was one order of magnitude better than that achieved without derivatization. The results of this study reveal the adequacy of the SPME–GC–MS method for analyzing bisphenol A leached from plastic containers. The concentrations of bisphenol A leached from plastic containers into water ranged from 0.7 to 78.5 μg L^?1.     

Study of a cysteine derivative as a corrosion inhibitor for carbon steel in phosphoric acid solution

Inhibition of corrosion of carbon steel in phosphoric acid solution by use of l-cysteine methyl ester hydrochloride has been investigated by measurement of weight loss and use of electrochemical methods. The efficiency of inhibition was increased by increasing the concentration of the inhibitor and reduced by increasing the temperature. Polarization studies revealed that this compound behaves as mixed-type inhibitor. Electrochemical impedance spectroscopy showed that dissolution of the steel occurs as a result of charge-transfer. Adsorption of the inhibitor obeyed the Langmuir adsorption isotherm. Kinetic and thermodynamic data were calculated and are discussed.     

Effect of pulegone and pulegone oxide on the corrosion of steel in 1 <Emphasis Type="Italic">M</Emphasis> HCl

The inhibitive action of pulegone and pulegone oxide toward acid corrosion of steel in molar hydrochloric acid was studied by weight loss measurements, potentiodynamic polarization, and impedance spectroscopy (EIS) methods. The pulegone is extracted starting from oil of Pennyroyal Mint (Mentha pulegium). The natural compound was found to delay the corrosion rate. The pulegone oxide is prepared by oxidation of pulegone. The inhibition efficiency was found to increase with the inhibitor content to attain 81 and 75% at 5 g dm⁻³ for pulegone and pulegone oxide. The increase in temperature leads to an increase in the inhibition efficiency of the natural compared. Correspondence: Belkheir Hammouti, Laboratoire de chimie Appliquée & Environnement, Faculté des Sciences, B.P. 717, 60000 Oujda, Morocco.     

Study of the inhibition of the corrosion of copper and zinc in HNO3 solution by electrochemical technique and quantum chemical calculations

The corrosion inhibition of copper and zinc in 0.1 M HNO₃ by 1,2,3,4-tetrazole (TTZ) and some of its derivatives has been analysed in a comparative study. Two experimental techniques have been used such as weight-loss and electrochemical polarization measurements. The results obtained reveal that the addition of these compounds reduces preferentially the corrosion of Cu rather than that of Zn. The adsorption of tetrazolic compounds on a copper surface was more favourable than their adsorption on a zinc surface. Moreover the inhibition efficiency calculated for copper was found to attain 95% in the presence of 1-phenyl-5-mercapto-1,2,3,4-tetrazole (PMT) while it remains constant at 1% for all compounds tested using zinc as electrode. Relationship between molecular structure and their inhibition efficiency was elucidated by quantum chemical calculations using the density functional theory (DFT).     

Biomimetic oxidation of catechol employing complexes formed in situ with heterocyclic ligands and different copper(II) salts

In the present work, catecholase activity is presented. The complexes were prepared by condensation of the organic ligand pyrazolyl L ₁ –L ₄ and copper(II) ion in situ. The pyrazolyl compounds L ₁ –L ₄ used in this study are: L ₁ is (3,5-dimethyl-pyrazol-1-ylmethyl)-(4-methyl-pyridin-2-yl)-pyrazol-1-ylmethyl-amine; L ₂ is 1-{4-[(3,5-dimethyl-pyrazol-1-ylmethyl)-pyrazol-1-ylmethyl-amino]-phenyl}-ethanone; L ₃ is 1-{4-[(3,5-dimethyl-pyrazol-1-ylmethyl)-[1,2,4]triazol-1-ylmethyl-amino]-phenyl}-ethanone, and L ₄ is 2-[(3,5-dimethyl-pyrazol-1-ylmethyl)-[1,2,4]triazol-1-ylmethyl-amino]-6-methyl-pyrimidin-4-ol, and copper ions salts Cu(II) are (Cu(CH₃COO)₂, CuCl₂, Cu(NO₃)₂ and CuSO₄). In order to determine factors influencing the catecholase activity of these complexes, the effect of ligand nature, ligand concentration, nature of solvent and nature of counter anion has been studied. The best activity of catechol oxidation is given by the combination formed by one equivalent of ligand L ₂ and one equivalent of Cu(CH₃COO)₂ in methanol solvent which is equal to 9.09 µmol L^?1 min^?1. The Michaelis–Menten model is applied for the best combination, to obtain the kinetic parameters, and we proposed the mechanism for oxidation reaction of catecholase.     

An Insight into All Tested Small Molecules against Fusarium oxysporum f. sp. Albedinis: A Comparative Review

Bayoud disease affects date palms in North Africa and the Middle East, and many researchers have used various methods to fight it. One of those methods is the chemical use of synthetic compounds, which raises questions centred around the compounds and common features used to prepare targeted molecules. In this review, 100 compounds of tested small molecules, collected from 2002 to 2022 in Web of Sciences, were divided into ten different classes against the main cause of Bayoud disease pathogen Fusarium oxysporum f. sp. albedinis (F.o.a.) with structure–activity relationship (SAR) interpretations for pharmacophore site predictions as (δ⁻···δ⁻), where 12 compounds are the most efficient (one compound from each group). The compounds, i.e., (Z)-1-(1.5-Dimethyl-1H-pyrazole-3-yl)-3-hydroxy but-2-en-1-one 7, (Z)-3-(phenyl)-1-(1,5-dimethyl-1H-pyrazole-3-yl)-3-hydroxyprop-2-en-1-one 23, (Z)-1-(1,5-Dimethyl-1H-pyrazole-3-yl)-3-hydroxy-3-(pyridine-2-yl)prop-2-en-1-one 29, and 2,3-bis-[(2-hydroxy-2-phenyl)ethenyl]-6-nitro-quinoxaline 61, have antifungal pharmacophore sites (δ⁻···δ⁻) in common in N1---O4, whereas other compounds have only one δ⁻ pharmacophore site pushed by the donor effect of the substituents on the phenyl rings. This specificity interferes in the biological activity against F.o.a. Further understanding of mechanistic drug–target interactions on this subject is currently underway.     

Synergistic effect of AM-4VP-9 copolymer and iodide ion on corrosion inhibition of mild steel in 1 M H2SO4

The effect of iodide ions on the corrosion inhibition of mild steel in 1 M sulfuric acid in the presence of poly(acrylamide-co-4-vinylpyridine) copolymer abbreviated by (AM-4VP-9) was studied by weight loss measurements and electrochemical techniques (impedance spectroscopy and polarisation curves) at 18 °C. The results obtained showed that the inhibition efficiency increased with increasing copolymer concentration. It was also found that the inhibition efficiency increased with the addition of potassium iodide (KI) to the copolymer. A synergistic effect was observed between the AM-4VP-9 copolymer and KI. On the other hand, it was found that the inhibiting effect of the system (AM-4VP-9 + KI) increased with increasing immersion time. Polarisation curves indicate that (AM-4VP-9) copolymer act as mixed inhibitors. EIS measurements show an increase of the transfer resistance with the inhibitor concentration.