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The purpose of this paper was to investigate the anti-corrosion behavior of polypyrrole (PPy) films in different states and presence of alumina nanoparticles synthesized by galvanostatic electropolymerization on stainless steel (SS) electrodes in an artificial seawater solution using potentiodynamic polarization and electrochemical impedance spectroscopy (EIS).

The electrochemical measurements were used to examine the effects of PPy and its nanocomposite on the corrosion behavior of SS type 316L in artificial seawater. A standard electrochemical cell with three electrodes was used for the measurements. The electrochemical response of the coated electrodes in the doped and the undoped state was compared with that of a bare electrode. Corrosion rate information was obtained by the Tafel extrapolation method, where the intersection point of a cathodic and an anodic polarization curve provides both the corrosion potential and the corrosion current. EIS measurements confirmed the potentiodynamic and open circuit potential (OCP) results. The microstructure of the obtained films was investigated by scanning electron microscopy.

The results showed that the coated polymer films shifted the electrode potential toward more positive potentials, but this shift did not lead to passivation. However, a notable synergy was observed between PPy undoped film, oxygen reduction and iron dissolution. The potential of the SS remained in the active dissolution region, and it was not possible to produce a passive oxide layer in this region. PPy separates the metal dissolution process from the oxygen reduction process. This would prevent the local pH increase at the metal surface and subsequent delamination. The polarization curves, EOCP and impedance measurements showed that PPy undoped/Al₂O₃ layers show promise as good candidates for the corrosion protection of reactive metals.

This paper presents that electrodes coated with undoped PPy synthesized in the presence of dodecyl sulfate anions and Al₂O₃ nanoparticles offered a noticeable enhancement of protection against corrosion processes.

Anodic behaviour of lead and lead alloys A guide to the use of lead and lead alloys as anodic materials in such processes as cathodic protection, electrolysis, electrosynthesis, electrodeposition, electrowinning, and pollution control has just been published by ERA.

This paper aims to investigate the electrocatalytic activity of CoFe_1.9Mo_0.1O₄-Ce_0.8Gd_0.18Ca_0.02O_2-δ composite (CFMo-CGDC) for the direct synthesis of ammonia from H₂O and N₂ under atmospheric pressure.

CoFe_1.9Mo_0.1O₄ nanoparticles (CFMo NPs) were synthesized via a sol-gel method. CFMo NPs were characterized using X-ray diffraction (XRD), Brunauer–Emmet–Teller (BET) specific surface area measurement and scanning electron microscope (SEM). Double-chamber reactor was used to synthesize ammonia using H₂O and N₂ as precursors. The factors affecting the ammonia formation rate (applied voltage and temperature) were studied.

CoFe_1.9Mo_0.1O₄ nanoparticles (CFMo NPs) were synthesized via a sol-gel method. CFMo NPs were characterized using XRD, Brunauer–Emmet–Teller (BET) specific surface area measurement and SEM. Double-chamber reactor was used to synthesize ammonia using H₂O and N₂ as precursors. The factors affecting the ammonia formation rate (applied voltage and temperature) were studied.

The usage of CFMo-CGDC composite as an electrocatalyst for the synthesis of ammonia directly from H₂O and N₂.

This work aims to prepare and characterize of protective anticorrosion phosphate-doped polyaniline (PANI) nanocomposite coatings for stainless steel (SS) in chloride solution.

PANI composite coatings were electrodeposited from aqueous sulfuric acid solution containing monomer and Al₂O₃ nanoparticles using cyclic voltammetry technique. Doping by phosphate was done by aging the coated steels for different periods (1–168 h) in phosphate solution. The polymer film composite was investigated by Fourier-transform infrared spectroscopy and scanning electron microscopy techniques. Potential-time, anodic polarization and electrochemical impedance spectroscopy were used to study the protection efficiency of the coatings.

The Al₂O₃ nanoparticles were incorporated into the deposited PANI layer but they decreased the deposition of polymer. The nanoparticles and the phosphate anions enhanced the protective PANI layer for passivation and protection of SS in the chloride solution.

The replacement of counter anions by phosphate ions improved significantly the PANI and its nanocomposite as protective coating of SS in chloride solution.

This paper aims to investigate the protection efficiency of a thin film of electrochemically synthesized conducting polymers, such as poly m‐toluidine, poly N‐methyl aniline, and its copolymer, poly (aniline‐co‐N‐methyl aniline) (PANINMA), on plain carbon steel in 0.1 M HCl. It also attempts to compare the protection efficiency of these compounds with polyaniline (PANI)‐coated carbon steel.

The green coloured and adherent coatings were obtained by cyclic voltammetry during sequential scanning of the potential region between −0.6 and 1.6 V at a scan rate of 10 mVs⁻¹. Potentiodynamic polarization measurement (DC) was used to obtain an estimate of the corrosion rate and protection efficiency for these electrodeposited polymers on the carbon steel. Scanning electron micrographs (SEM) also were obtained to characterize the deposited coatings.

It was observed that these polymer coatings showed better protection efficiency than the PANI coating. Of the compounds studied, the copolymer PANINMA coating showed higher protection efficiency than other coatings. The SEM observations revealed that the compact continuous dense morphology of PANINMA provided better protection than other coatings.

This paper explains the protection efficiency of the substituted and copolymer coatings of PANI on carbon steel.

In view of the increasing use of the potentiostat, both as a research tool and for accelerated testing of materials, it is felt that a guide along the lines of ‘Have potentiostat, will corrode’ would be useful to both new workers in this field as well as to established corrosion engineers. The magnitude of the subject precludes a detailed discussion and therefore this article is intended to be an introduction rather than a critical appraisal. The current developments in potentiostatic techniques and instrumentation were recently discussed at a Corrosion and Protection Association symposium. (The present article is based on one of the papers.)

The effect of oxalic acid (OA) on corrosion resistance of carbon steel in sulphuric acid pH=2.5‐6.0 solutions containing 10⁻⁷‐10⁻³M OA was investigated by means of potentiodynamic polarisation measurements and immersion tests. The results suggest that OA is a good corrosion inhibitor for carbon steel, exhibiting inhibition efficiencies (IE) ranging from 50 to 85 per cent in dilute 10⁻⁷‐10⁻⁵M OA solutions of pH>3.0, whereas for pH≤3.0 solutions, an increase in corrosion rate was found. Non‐accelerated experiments (weight loss tests) carried out by immersing carbon steel specimens into OA‐containing solutions during at least 6 h revealed only positive IE values, regardless of both solution pH and OA content. The results were explained considering the solution composition as function of pH.

The purpose of this study is to study corrosion inhibition of Bronze alloy B66 by 4-amino-3-methyl-1,2,4-triazole-5-thione (MTSNH) in 3 per cent NaCl solution. Archaeological bronze artefacts often are stored or displayed in uncontrolled conditions and may suffer from dangerous active corrosion processes that can lead to their destruction. The most dangerous form of archaeological bronze degradation is due to a cyclic reaction that involves copper from the pure alloy and chlorine as a pathogenic agent. A protection treatment can be used to protect them from the corrosion environment and stabilise them to avoid further degradation during exhibition or storage. Starting from its initial assessment as a corrosion inhibitor for pure copper, nowadays benzotriazole (BTA) is in widespread use for the conservation of copper-based artefacts, but unfortunately, BTA is toxic and a suspected carcinogen. The development of new and safe protection systems would offer a choice of alternative products to conservation-restoration professionals for the effective and safe stabilization and protection of metal artefacts. In this investigation, a new organic compound, namely, MTSNH, was synthesized, characterized and tested as a corrosion inhibitor for Bronze B66 (similar to archaeological bronze) in 3 per cent NaCl solution using potentiodynamic polarization studies and electrochemical impedance spectroscopy (EIS) at room temperature. It has been observed from the corrosion rate that the inhibition efficiency increased with increasing concentration of MTSNH. Potentiodynamic polarisation results revealed that the compound acted as a mixed-type inhibitor. Impedance studies indicated that protection occurs through adsorption of the inhibitor on the metal surface, with important modification to the mechanism of corrosion. Surface analysis was carried out using scanning electron microscopy scanning electron microscopy (SEM)/energy dispersive spectrometry (EDX) techniques to verify the electrochemical results.

The inhibition efficiency of MTSNH is investigated by potentiodynamic polarization, EIS and surface analysis.

The synthesized MTSNH act a good inhibitor in 3 per cent NaCl and inhibition efficiency increases with inhibitor concentration. Polarisation curves showed that the inhibitor is mixed. The EIS measurements showed that the inhibitor acted throughout the formation of film at the bronze surface. The surface analysis confirms this result.

The adsorption of the MTSNH on the metal surface can markedly change the corrosion resisting property of metal. Therefore, the study of the relation between adsorption and corrosion inhibiting is of a great importance.