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The paper introduces a microwave and electrochemical-assisted method for synthesis of chlorine-derived iron phthalocyanine pigment and oxygen reduction reaction catalyst nanoparticles. The aims of this study are to investigate the possibility of nano-scale particle size (<35 nm), high-efficiency product reaction, remove acidic wastewater, time optimization and maximize number of chlorine on aromatic rings.

The paper presents a combined synthesis technique, which does not have the problems of the conventional methods. Chlorinated iron phthalocyanine nanoparticles have been fabricated using phthalic anhydride, urea (high purity), electrochemical-generated iron (II) cations and microwave irradiation as promoter. The approach yields a product of high quality, uniform particle size distribution and high efficiency and that was environment-friendly.

The particle size and time needed for the production of chlorinated iron phthalocyanine were about 35 nm and 7 min, respectively.

The catalyst, that is used in this method, should be weighed carefully. In addition, the solvent should be a saturated solution of NaCl in water.

The method provides a simple and practical solution to improving the synthesis of an iron-based catalyst for oxygen reduction reaction.

The combined method for synthesis of chlorinated iron phthalocyanine was novel and can find numerous applications in the industry, especially as an oxygen reduction reaction non-precious metal catalyst.

This study aims to develops a new-type low-alloy corrosion resistant steel containing Sb and investigate the corrosion mechanism of this new-type low-alloy steel.

Energy dispersive spectrometer, X-ray photoelectron spectroscopy, X-Ray diffraction and scanning electron microscopy were used to evaluate the corrosion resistance of the rust layers formed on these samples. Laser confocal microscopy was used to observe the corroded surfaces of the steels.

Results showed that Sb added can consume H⁺ in the solution, thereby preventing the oxygen reaction to slow down the corrosion rate. Meanwhile, a stable and insoluble substance (Sb₂O₃) in the acidic solution would be produced when the reaction of the product of Sb and H⁺ with the enough dissolved oxygen in the solution. Due to the precipitation of Sb₂O₃ and iron oxyhydroxides, the rust layer of Sb-containing steel became more uniform and compact, which resulted in better corrosion resistance in acid environment.

In this study, a new-type acid resistant low-alloy steel containing Sb was developed. Compared with the results, the corrosion mechanism of the new-type low-alloy steel in acid environment was discussed.

In general, whenever water and metals are in contact with each other in the presence of air and dissolved salts, corrosion will usually occur. The critical factors in this situation will be the nature of the metal, the composition of the water, i.e. its pH, conductivity, the concentration and the composition of the dissolved salts, and the temperature. Elevated temperatures, as in boiler water systems, exacerbate any corrosion problems.

The purpose of this paper is to introduce bio-inspired FeN₄-S-C black nano-electrocatalyst for the oxygen reduction reaction (ORR) in an alkaline medium. The FeN₄-S-C derived without pyrolysis of precursors in high temperature is recognized as a new electrocatalyst for the ORR in an alkaline electrolyte. For the proper design of bio-inspired nano-electrocatalyst for the ORR performance, chlorinated iron (II) phthalocyanine nanoparticles were used as templates for achieving the active sites in aqueous KOH by rotating disk electrode methods. The most active FeN₄-S-C catalyst exhibited a remarkable ORR activity in the alkaline medium. The objectives of this paper are to investigate the possibility of nanoscale particles size (Ëœ5nm) of electrocatalyst, to achieve four-electron transfer mechanism and to exhibit much superior catalytic stability in measurements. This paper will shed light on bio-inspired FeN₄-S-C materials for the ORR catalysis in alkaline fuel cells.

The paper presents a new bio-inspired nano-electrocatalyst for the ORR, which has activity nearby platinum/carbon electrocatalyst. Chlorinated iron phthalocyanine nanoparticles have been used as FeN₄ template, which is the key point for the ORR. Bio-inspired nano-electrocatalyst has been fabricated using chlorinated iron phthalocyanine, sodium sulphide and carbon black.

The particles’ size was 5 nm and electron transfer number was 4.

The catalyst that is used in this method should be weighed carefully. In addition, the solvent should be a saturated solution of NaCl in water.

The method provides a simple and practical solution to improving the synthesis of iron-based catalyst for ORR.

The method for the synthesis of bio-inspired electrocatalyst was novel and can find numerous applications in industries, especially as ORR non-precious metal catalyst.

The aim of the present work was to study the synergistic effect of HEDP and zinc on inhibition of the corrosion of carbon steel in neutral oxygen‐containing chloride solutions, and to investigate the effect of zinc‐HEDP molar ratio on the effectiveness of the zinc‐HEDP inhibitive mixtures.

The inhibition of the corrosion of carbon steel by zinc‐HEDP mixtures in neutral oxygen‐containing solutions was investigated in the presence of 0.003 M (106 ppm) chloride.

It was shown that the inhibition by these mixtures depended not only on the zinc/HEDP molar ratio but also on the concentration of both zinc and HEDP. HEDP concentration appeared to be crucial where good inhibition was not achieved at low concentrations and aggressive nature is observed at high HEDP levels. The effectiveness of the zinc‐HEDP mixtures enhanced inhibition by increasing the zinc content of the mixture, but the mechanism was only effective to a certain level, above which the inhibition effect declined. The predominant corrosion control mechanism of the zinc‐HEDP mixture was on the anodic (metal dissolution) reaction, but it also affected the rate and mechanism of the oxygen reduction reaction.

Demonstrates how the effectiveness of the zinc‐HEDP mixtures can enhance inhibition by increasing the zinc content of the mixture.

The purpose of this paper was to study the parameters affecting corrosion of the closed-loop oscillating heat-pipe with check valves (CLOHP/CV) in a system in clear that will be basic data to be used in future research. The majority of research focuses on the inner surface corrosion heat-pipe systems. The CLOHP/CV is commonly favored in cooling electronic devices, etc. Despite these common applications, limited reliable experimental research findings are available on the operation of the CLOHP/CV. Because of these reasons, the lack of detailed data, working fluids effect, working temperatures and duration of testing of the CLOHP/CV, this study focuses on determining the actual inner surface corrosion.

Seven types of copper tubes used in the CLOHP/CV set were sectioned to observe their inner surfaces. Seven different specimens with tube corrosion were examined by a visual inspection, scanning electron microscopy (SEM) and energy dispersive X-ray spectrometry (EDX). The technique for detecting metals solution in samples is based on the fact that ground state metals absorb light at specific wavelengths. Metal ions in a solution are converted to atomic state by means of a flame. In this study, concentration of copper particle in the working fluid was found by flame atomic absorption spectroscopy (Flame-AAS) and elements that occurred on inner surface tube were analyzed by EDX.

The analyses with SEM and EDX testing found that the character corrosion of inner surface of CLOHP/CV was pitting clearly. The analysis with Flame-AAS found that the concentration of copper particles in the distilled water and ethanol as working fluid is more than after 1,000 hours until 3,000 hours because of excess volume of oxygen in working fluid which causes many reactions at the beginning. When the oxygen decreases after 1,000 hours, it causes the reaction to decrease too and get the most concentration of copper particles, i.e. 18.57228 ppm or 0.40859 mg.

Corrosion-dependant maintenance must also be factored into the design. Producing reliable equipment that will become standardized and fixing the time for proper maintenance will require individuals that are knowledgeable about the materials that are going to be used in the design of such equipment. Nowadays, the lack of detailed data of working fluids effect, working temperatures and duration of testing of the CLOHP/CV focuses on determining the actual inner surface corrosion. Therefore, this research aimed to study the parameters affecting corrosion of the CLOHP/CV in a system in clear that will be basic data to be used in future research.

The purpose of this paper is to investigate the influence of the potential of hydrogen (pH) and dissolved oxygen in artificial seawater on the passivation behavior of 316L stainless steel.

The corrosion behavior was studied by using electrochemical measurements such as electrochemical impedance spectroscopy and polarization curve. The passive films were characterized with X-ray photoelectron spectroscopy.

The polarization resistance of the passive film decreases as the pH value drops ascribed to the formation of much more point defects. The donor carrier concentration (ND) in the passive film formed in the deaerated condition is lower than that in aerated conditions. Nevertheless, this phenomenon is the opposite when the pH value is 1 due to the significant decrease of Fe oxides/hydroxides coupled with the stable content of Cr oxides/hydroxides species. In addition, the compositional variation of the passive film also leads to the changes of its semiconductor properties from N-type to bipolar type.

This paper shows the variation of polarization resistance, corrosion potential, passive film composition and semiconductor properties with the pH value and dissolved oxygen. The results can serve as references to the further study on crevice corrosion of 316L in seawater.

The purpose of this paper is to investigate the inhibition effect of cysteine on the corrosion behaviour of copper in 3.5% NaCl solution with and without cysteine.

For this purpose, potentiodynamic polarization curves and electrochemical impedance spectroscopy (EIS) techniques were used. The surface morphology of the metal sample after exposure to the corrosive medium was investigated by scanning electron microscopy (SEM). The effect of temperature also was studied over the range 298‐328 K. Thermodynamic parameters (ΔG, ΔH and ΔS) were calculated and discussed.

It was found that cysteine could inhibit the corrosion of copper in 3.5% NaCl solution. Cysteine is an organic corrosion inhibitor for copper, and its molecules are physically adsorbed to form a protective film. Inhibition efficiency increases with decreasing cysteine concentration and the product behaves as an anodic‐type inhibitor.

In this study, the inhibitory effect of cysteine with temperature change was investigated in environments containing 10⁻² M cysteine solution at pH 8.5.

It will be possible to replace other inhibitors, with cysteine for copper protection in heating/cooling systems at higher temperatures.

Cysteine acts as an anodic inhibitor especially for copper‐based materials in acidic solution. The interaction between the cysteine molecule and copper in alkaline media has not been investigated in detail. The main objectives of this study was to gain some insight into the protection of copper by cysteine in 3.5% NaCl medium at a pH value of 8.5.

The purpose of this paper is to study the susceptibility of these three commonly used corrosion resistance fasteners in seawater. For a more practical scenario, a local Atlantic coastal seawater as received was used.

Carbon fiber reinforced polymer (CFRP) was fabricated with T700 carbon fiber (Toray Inc.) and VE8084 vinyl ester resin (Ashland) to make a unidirectional composite panel of thickness 1.8 mm. A conductive paint was applied to one of the sample edges that was perpendicular to the fiber direction, providing an electrical contact with carbon fibers to connect a copper wire. This external electric connection was used for potential measurements of both the open circuit potential (OCP) of the CFRP sample, and the mixed potential of the fastened set: consisting of the CFRP and the metallic fastener fastened to it. Three common fastener alloys were selected: 316SS, Monel and Titanium. For this purpose, a high impedance voltmeter was used in conjunction with a saturated calomel reference electrode. Measurements were taken daily. For longer time measurements, a four-channel high impedance analog data logger was used with 30 min sampling rate.

For both 316SS and Monel fastened sets, crevice corrosion occurred inside the occluded regions of the set, when immersed in coastal seawater. The attack was more severe for 316 stainless steel set. An isolated island attack of faceted surfaces morphology was seen for 316SS set. While, a circular ring of preferential grain boundary attack appeared for Monel set, indicating an IR (voltage) drop mechanism is more likely operating. Titanium-fastened sets showed high resistance to crevice corrosion when simmered in seawater. However, for long-time exposure, the sets became more susceptible to crevice corrosion attack supported by CFRP attachment (oxygen reduction reaction taking place at the carbon fibers).

Evidently, titanium, stainless steels and Monel are good candidates for galvanic corrosion resistance. However, their susceptibility to crevice corrosion when coupled with CFRP is a new challenging topic that needs further investigation. This is very important today because the vast application witnessed for CFRP material. This work involves developing an original methodology for this kind of investigation and was done at advanced laboratories of SeaTech at Florida Atlantic University by the Atlantic coastline.

This paper aims to study the corrosion behavior of D32 steel suffered to marine splash zone. Type D32 structural steel has good mechanical properties and is commonly used for offshore oil platform construction in China. To ensure the safety of marine steel structure, it is important to study the corrosion process of D32 steel in the splash zone.

The corrosion behavior of D32 steel in splash zone environments was studied using polarization curves and electrochemical impedance spectroscopy. The electrochemical results were obtained from the corroded steel samples exposed in the splash zone of a bespoke simulate device, while corrosion morphologies and corrosion products of the steel samples were characterized using scanning electron microscopy and X-ray diffraction.

In wet–dry cyclic exposure, the reaction was a self-perpetuating process of chemical oxidation and electrochemical reduction. The rust itself took part in the reduction processes and, hence, increased the corrosion rate of the steel samples.

Finally, the corrosion process of D32 steel in splash zone is considered.