Portugaliae
Electrochimica Acta

The inhibition performance of a non-oxidising surfactant, namely cetyl trimethyl ammonium bromide (CTAB), and its co-adsorption behaviour with zinc ion on carbon steel in well water was studied by potentiodynamic polarization, electrochemical impedance spectroscopy (EIS), weight loss, as well as atomic force microscopy (AFM) and scanning electron microscopy. Results indicated that the formulation acted as an anodic inhibitor. Adsorption of the used inhibitor led to a reduction in the double layer capacitance and an increase in the charge transfer resistance. A synergistic effect was also observed for the studied inhibitor with Zn(II) in weight loss measurements and electrochemical studies.

The inhibition effect of Mentha pulegium extract (MPE) on the acid corrosion of carbon steel in 1 M HCl solution was investigated using weight loss, potentiodynamic polarisation, and electrochemical impedance spectroscopy. The results show that the Mentha pulegium extract is a good inhibitor, and that the inhibition efficiency depends on the concentration of the plant extract. Efficiency is higher than 88 % for 33% Mentha pulegium extract. Polarization measurements also show that Mentha pulegium extract is a good mixed inhibitor. The remarkable inhibition efficiency of MPE was discussed in terms of blocking of the electrode surface by adsorption of inhibitor molecules through active centres. Mentha pulegium extract is adsorbed on the carbon steel surface according to the Temkin adsorption model. The effect of temperature on the corrosion behaviour of carbon steel in 1 M HCl with addition of 33% MPE was studied in the temperature range 308-338 K. SEM also confirmed the adsorption of MPE on carbon steel surface.

In this study polypyrrole (PPy) bilayers films were electrodeposited onto SAE 4140 steel. The inner layer was electropolymerized in the presence of molibdate and nitrate and the outer layer in a solution containing sodium bis (2-ethylhexyl) sulfosuccinate (AOT). The electrosynthesis was done under potentiostatic conditions. The corrosion protection properties of the films were examined in sodium chloride solution by open circuit measurements, linear polarization and electrochemical impedance spectroscopy (EIS). The bilayer coatings present an improved anticorrosive performance with respect to single PPy films.

Electroreduction properties of salicylic (SA) and acetylsalicylic (ASA) acids were investigated at platinum electrode using the voltammetry method. Cyclic voltammograms (CV) of the tested compounds were used in determining half-wave potential (E1/2) - the parameter describing the anti-reductive properties. The content of active substances (SA and ASA) in the selected pharmaceuticals (salicylic alcohol, Bayer aspirin, etopirin and polopirin) was examined with the application of electrochemical and spectrophotometric methods.

Examination of the physical (colour, odour, pH, solubility in various solvents) and chemical (GCMS and FTIR) characteristics of Ficus benjamina gum revealed that the gum is yellowish in colour, mildly acidic and ionic in nature. Major constituents of the gums were found to be sucrose and d-glucose, which constituted 60.92 % of their chemical constituents, while various carboxylic acids [(albietic acid (1.00%), hexadecanoic acid (4.41 %), 9-octadecanoic acid (1.00 %), octadecanoic acid (3.01 %), oleic acid (0.10 %), octadecanoic acid (9.12 %) and 6,13-pentacenequinone (20.43 %)] accounted for the remaining constituents. Functional groups identified in the gum were found to be those typical for other carbohydrates. From the knowledge of the chemical structures of compounds that constitute the gum, the corrosion inhibition potentials of the gum were ascertained and from weight loss analysis, the gum was found to be an active inhibitor against the corrosion of aluminum in solutions of tetraoxosulphate (VI) acid. The gum acted as an adsorption inhibitor that favours the mechanism of chemical adsorption and supported the Frumkin and Dubinin-Radushkevich adsorption models.

Electrochemical monitoring techniques were employed in this study to assess anticorrosion performance of Phyllanthus muellerianus leaf-extract on concrete steel-reinforcement in 0.5 M H2SO4, used for simulating industrial/microbial environment. For this, steel-reinforced concretes admixed with different concentrations of the natural plant leaf-extract were partially immersed in the acidic test-solution and subjected to electrochemical monitoring of corrosion potential, corrosion current and corrosion rate. Test responses analysed as per ASTM G16¬-95 R04, showed that the corrosion rate correlated, r = 84.93%, ANOVA p-value = 0.0403, with the leaf-extract concentration admixed in concrete and the ratio of the standard deviation of potential to the standard deviation of current. These identified the 0.3333% Phyllanthus muellerianus (per weight of cement) with optimum effectiveness at inhibiting steel-reinforcement corrosion both by the experimental model, η = 91.662.51%, and by the prediction from the correlation fitting model, η = 85.5414.44%. Fittings of both the experimental and the predicted data followed the Flory–Huggins and the Frumkin adsorption isotherms which suggest prevalent mechanism of physical adsorption (physisorption) of the extract on steel-rebar surface. These support the use of Phyllanthus muellerianus as environmentally-friendly admixture for inhibiting concrete steel-reinforcement corrosion in the industrial/microbial service-environment.

The influence of cathode material on the electrochemical degradation of methyl orange (MO), methylene blue (MB) and malachite green (MG) dyes was investigated. The cathode materials used were platinum (Pt), copper (Cu), zinc (Zn) and aluminum (Al). The electrochemical activity of the selected dyes on the metal cathodes was examined by cyclic voltammetry (CV). The electrochemical treatment was carried out in both divided and undivided cells. The degradation process was monitored by UV-Visible spectroscopy and chemical oxygen demand (COD) measurement. The influence of pH on discoloration and degradation of dyes was studied. The power consumption and current efficiency of the treatment process involving different cathode materials was computed and compared. The role of cathode material in the degradation of dyes has been established.

The degradation of Alizarin Red S by electro-generated species using Pt and BDD electrodes was performed. The results were explained by the generation of OH* radical, S2O82− at BDD electrode and active chlorine species at Pt electrode. The slow degradation is affected by the current density, initial pH, temperature, initial dye concentration and the nature of the supporting electrolyte. However, the ionic strength showed a negligible effect on both electrodes. In the presence of KCl, the intermediates produced during the degradation are similar at both electrodes. In the presence of sulfate (at BDD electrode), the rate and the mechanism of the degradation are different from those in the presence of KCl. TOC analysis showed total mineralization of AR S.

The perovskite BaPb0.9Sb0.1O3 was prepared through the ceramic route and, after being chemical, structural and electrochemically characterized, it was used in the electrochemical oxidation of guaiacol, using Na2SO4 as electrolyte, at current densities of 5 and 10 mA cm-2 and initial guaiacol concentrations of 50, 100 and 200 mg L-1. The guaiacol degradation was followed by UV-Visible absorbance measurements, Chemical Oxygen Demand (COD) tests and Dissolved Organic Carbon (DOC) analysis. The combustion efficiency was also determined. Results have shown COD removals between 40 and 85 % and DOC removals from 34 to 66 % after 120 h assays. The absolute COD and DOC removals increase with guaiacol initial concentration and applied current density. The mineralization tendency, measured as the combustion efficiency, was maximum for the applied current density of 10 mA cm-2 and a guaiacol initial concentration of 200 mg L-1.

The influence of 2,6-bis-(hydroxy)-pyridine (P1), 2,6-bis-(chloro)-pyridine (P2) and diethyl 1,1’-(pyridine-2,6-diyl)bis(5-methyl-1H-pyrazol2-3-carboxylate ( P3) on the corrosion of steel in 1 N HCl solution has been studied by weight loss measurements, potentiodynamic and impedance spectroscopy methods. The inhibiting action increases with the concentration of these compounds to attain 91,5% at 10-3 M for P3. We note good agreement between gravimetric and electrochemical methods. The polarisation measurements show also that the pyridines act essentially as mixed inhibitors and the cathodic curves indicate that the reduction of proton at the steel surface happens with an activating mechanism. The temperature effect on the corrosion behaviour of iron in 1 M HCl without and with these inhibitors at different concentrations was studied in the temperature range from 313 to 353 K, and allows deducing the apparent activation energy, enthalpy and entropy of the dissolution process and the free energy were determined and discussed. The inhibitors were adsorbed on the iron surface according to the Langmuir adsorption isotherm model at different temperatures and some thermodynamic data for the adsorption process are calculated. The experimental study has been finished by quantum theoretical study; the quantum chemical calculations, based on DFT methods at B3LYP/6-31G** level of theory, were performed, by means of the GAUSSIAN 03 set of programs. Structural parameters, such as the frontier molecular orbital energies (EHOMO and ELUMO), gap of energy E, charge distribution, absolute hardness η and softens , fraction of electrons N transferred from pyridine molecules to steel, as well as electronic parameters such as Mulliken atomic populations have been determined. The objective of this quantum theoretical treatment is to attempt to find relationships between their molecular and electronic structures and inhibition efficiency.

The inhibition action of the Pyrazolone Derivative (PYR) on the corrosion of mild steel in 0.5 M sulphuric acid was investigated by weight loss, polarization, impedance and SEM. Results obtained revealed that PYR performed excellently as corrosion inhibitor with efficiency of 91% at 11 ppm at 298 K. Its adsorption on mild steel obeys Langmuir and Temkin isotherm. Polarization curves indicate that PYR behaves as mixed type. The value of ∆G°ads indicates the spontaneous physisorption of PYR. The SEM results confirm the presence of a protective surface layer over the mild steel surface. The reactivity of the compound was analysed through theoretical calculation.

In this study, we investigated the use of ion exchange processes using a chelating resin, Diaion CRB02 for the removal of boron from the bittern solution left after the extraction of sodium sulfate and sodium chloride from the water of Lake Qarun, located in Egypt. The effects of parameters such as the initial boron concentration and the pH value on the breakthrough volume were studied using boric acid as the synthetic simulant of the bittern solution. The breakthrough capacity was shown to be directly proportional to the height of the resin bed and inversely proportional to the initial boron concentration and the feed flow rate. In addition, the optimum pH for boron removal was found to be 10. An electrically assisted process, which had been found to be effective for a strongly acidic cation exchange resin, was also applied to the ion exchange by taking the electric current as a parameter. However, no remarkable effect was observed, which may result from the difference in the function group between an ion exchange resin using electrostatic attractive force and a chelating resin using complex formation.

Electroless Ni–P based composite coatings are more popular due to their excellent hardness, yield strength, wear resistance, frictional resistance, corrosion resistance, and good lubricity. The present study deals with significance of various coating process parameters on the corrosion behavior of the Ni–P–Al2O3 composite coatings on mild steel substrate. Corrosion behavior of the composite coatings after heat treatment at various annealing temperatures (300 °C, 400 °C, and 500 °C) are investigated by potentiodynamic polarization test using 3.5% NaCl solution. For maximization of corrosion resistance, the electrochemical parameters, corrosion potential (Ecorr) and corrosion current density (Icorr), are optimized using Taguchi based grey relational analysis. For optimization four coating process parameters are considered, namely, concentration of nickel source, concentration of reducing agent, concentration of second phase particles (alumina particles), and annealing temperature, as main design factors. The optimum combinations of the said design factors are obtained from the analysis. Analysis of variance (ANOVA) reveals that the concentration of alumina particles and annealing temperature has the significant influence on the corrosion resistance of the composite coatings. The microstructure of the surface is studied by scanning electron microscopy (SEM) and chemical composition is studied by energy dispersive X–ray analysis (EDX). The X–ray diffraction analysis (XRD) is used to identify the phase transformation behavior of the composite coatings.

Cashew nut testa tannin [CASTAN] has been found to inhibit the corrosion of aluminium in hydrochloric acid solutions using gravimetric, thermometric and UV/visible spectrophotometric techniques. CASTAN inhibition was by adsorption on aluminium following Temkin isotherm in 0.1 M HCl and Langmuir isotherm in 0.5 M and 2.0 M HCl at 303 Kelvin. Physical adsorption on aluminium has been proposed in studied HCl solutions; therefore, CASTAN is a cathodic inhibitor. Earlier reports [1] showed CASTAN to contain quercetin, azaleatin, catechin, epicatechin, cyanidin and delphinidin. However, UV/visible spectrophotometric analysis of CASTAN in ethanol reveals quercetin as its major component. This work therefore investigated the correlation between computed molecular parameters and inhibitive properties of CASTAN and adsorption sites on its components. Calculated quantum chemical parameters namely: EHOMO (highest occupied molecular orbital energy), ELUMO (lowest unoccupied molecular orbital energy), energy gap (ΔE) and dipole moment ( ) suggest that CASTAN is a soft inhibitor and it’s components inhibited aluminium corrosion in protonated forms. Calculated Mulliken charges implicated some electron rich sites, namely: the aromatic and conjugated C=C, C=O and O-H as adsorption sites on the inhibitor molecules. Proposed kinetic model reveals complex reaction mechanism, parallel reactions, for aluminium corrosion inhibition by CASTAN.

The effect of the phenolic (OOMW-Ph) and non-phenolic (OOMW-NPh) fractions of the extract of olive oil mill wastewaters was evaluated as corrosion inhibitor of steel in molar hydrochloric using weight loss measurements and electrochemical polarisation. The results obtained reveal that the referred compounds reduce the corrosion rate. The inhibiting action increases with the concentration of the extract compounds to attain 88.9% and 89.1% of OOMW-Ph and OOMW-NPh, respectively. The increase in temperature leads to a decrease in the inhibition efficiency of the compounds in the temperature range 303 at 333 K. The adsorption isotherm of the inhibitors on the steel surface has been determined. The thermodynamic data of activation and adsorption are determined as well. The phenolic compound (bioactive) most abundant in OOMW extracts is hydroxytyrosol (4 - (2-hydroxyethyl) -1, 2-benzenediol), playing an important role in the effect of the anti-corrosion, either alone or in synergy with other two compounds (tyrosol and oleuropein (4 - (2-hydroxyethyl) phenol) which are present with considerable amounts.

Electrochemical metal nucleation is the method for the formation of metal nanoparticles on the electrode surface. Studying the early stage of electronucleation is simpler than other methods as the driving force for nucleation is achieved by changing deposition potentials and concentration of metal ions. In this work, the potential step electrochemical deposition of palladium was studied from its chloride solution at room temperature on glassy carbon electrode surface. The nucleation mechanism was studied by analysis of the resulting current transients. Accordingly, the initial electro-nucleation mechanism of palladium nanoparticles was found to be varying depending on deposition conditions such as deposition potential and palladium concentration. It can be changed from 3D instantaneous (for all deposition potentials studied and in higher electrolytic concentration) to 3D progressive nucleation mechanism (for lower deposition potential and lower electrolytic concentration). In addition, the nucleation rate for each deposition potential as well as the concentration has been determined. The nucleation rate in this research is used to calculate the nuclei density and found to decrease from more negative deposition potential to more positive deposition potential in agreement with the observed shift in electronucleation mechanism.

The inhibition of the corrosion of Mild Steel (MS) in 1 M HCl solution by a new synthesised organic compound, namely 1,1'-(2,2'-(2,2'-oxybis(ethane-2,1-diyl)bis (sulfanediyl))bis(ethane-2,1-diyl))diazepan-2-one, has been studied by weight loss measurements, electrochemical polarisation and electrochemical impedance spectroscopy (EIS). The experimental results have showed that this organic compound revealed a good corrosion inhibition and the inhibition efficiency is increased with the inhibitor concentration to reach 97% at 1 mM. Potentiodynamic polarisation suggested that it is a mixed type of inhibitor. EIS measurements show an increase of the polarisation resistance with the inhibitor concentration and the electrical equivalent circuit is determined. The inhibitor adsorption process on (MS) surfaces obeys the Langmuir adsorption isotherm and the adsorption isotherm parameters (Kads, ΔGads, ΔHads and ΔSads) were determined. The temperature effect on the corrosion behaviour of (MS) in 1 M HCl without and with inhibitor at different concentration was studied in the temperature range from 308 to 353 K and the kinetic parameters activation such as Ea, ΔHa and ΔSa were evaluated.

Adsorptive stripping voltammetry was used to prospect the adsorption property of montelukast sodium (MKST) on the hanging mercury drop electrode (HMDE). Through appointing the adsorptive stripping voltammetric (AdSV) process, a sensitive electroanalytical method for the quantitative analysis of MKST was accomplished. A well-developed voltammetric peak was obtained in pH 10 Britton-Robinson buffer (B-R buffer) at -1.080 V. The cyclic voltammetric studies indicated that the reduction process was irreversible and primarily controlled by adsorption phenomena. The studies of the variation of adsorptive voltammetric peak current with buffer electrolyte, pH, accumulation time (tacc), accumulation potential (Eacc), sweep rate, pulse amplitude, square wave frequency, working electrode area and convection rate have evaluated in the recognition of optimal experimental conditions for MKST analysis. The studied electroanalytical signal showed a linear response for MKST in the concentration range 510-8- 110-6 mol L-1 (r = 0.994). A detection limit of 410-9 mol L-1 with relative standard deviation of 1.1 RSD% and mean recovery of 102%±2.0 were obtained. The possible interferences by several compounds usually present in the pharmaceutical formulation were also evaluated. The analytical quantification of MKST drug in commercially available pharmaceutical formulation and biological samples was electrochemically studied.

Lead present in several industrial wastes has deleterious effects on the quality of water. Cathodic deposition has been considered as one of the suitable means for lead removal. Experiments were carried out using a lab-scale electrochemical cell incorporating flow-by porous graphite electrodes at steady state conditions. The effects of flow rate, current density, lead influent concentration and pH, on lead removal efficiency, current efficiency, lead removal rates, and cell potential, were investigated. It was found that the maximum removal efficiency (97.75%) was obtained at flow rate (100 mL/min), for initial concentration (40 mg/L), with a residual concentration (0.9 mg/L) and maximum current efficiency of (60.7%). In addition, the recovery of lead from wastewater was investigated.

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