ELECTROCHEMICAL MEASUREMENTS OF COMPONENT ACTIVITIES IN METALLURGICAL SLAGS

The up-to-date status of FeO, CaO, SiO2, P2O5, Ti2O3 and Cr2O3 activity measurements in metallurgical slags using electrochemical sensors is outlined. A description of theoretical concepts and practical sensors is presented including their determining features.

Corrosion Measurements of Reinforcing Steel by Different Electrochemical Techniques

Electrochemical techniques of the corrosion measurements of reinforcing steeI in concrete have been evaluated. These techniques include half-cell potential measurements, impressed voltage method, impressed current method and potentiostatic polarization technique. The results of corrosion behaviour of the steel in both 5%NaCl and 5%MgSO4 show that each electrochemical technique provides some information about the condition of the steel bar or the corrosivity of the environment being evaluated, yet none provides a complete data regarding the corrosion resistance of reinforcing steel in aggressive media

Bioleaching and electrochemical property of marmatite by Leptospirillum ferrooxidans

The effects of several variables on the bioleaching of marmatite with pure L. ferrooxidans were investigated. The results show that zinc extraction increases with the decrease of pulp density. Adjusting pH tol.6 during the bioleaching process has a positive effect to the dissolution of marmatite. External addition of Fe^3＋ ions accelerates the bioleaching, while the concentration of additional Fe^3＋ over 2.5 g/L weakens the acceleration effect due to the inhibition effect on bacteria growth and the promotion of jarosite production. The electrochemical measurements were used to make further understanding on the dissolution of marmatite with and without additional Fe^3＋ in the presence of L. ferrooxidans. The experimental data illustrate that additional Fe^3＋ ions could increase the corrosion current density, which is favorable to zinc extraction. The EIS spectra show that rate-limiting step does not change when Fe^3＋ is added.

Electrochemical behavior of mesh and plate oxide coated anodes during zinc electrowinning

The catalytic performance of two oxides coated anodes （OCSs） meshes and one OCA plate was investigated in a zinc electrowinning electrolyte at 38 ℃. Their electrochemical behaviors were compared with that of a conventional Pb-0.7%Ag alloy anode. Electrochemical measurements such as cyclic voltammetric, galvanostatic, potentiodynamic, open-circuit potential （OCP） and in situ electrochemical noise measurements were considered. After 2 h of OCP test, the linear polarization shows that the corrosion current density of the Ti/（IrO2-Ta2O5） mesh electrode is the lowest （3.37μA/cm^2） among the three OCAs and shows excellent performance. Additionally, after 24 h of galvanostatic polarization at 50 mA/cm^2and 38 ℃, the Ti/MnO2mesh anode has the highest potential （1.799 V）, followed by the Ti/（IrO2-Ta2O5） plate （1.775 V） and Ti/（IrO2-Ta2O5） mesh （1.705 V） anodes. After 24 h of galvanostatic polarization followed by 16 h of decay, the linear polarization method confirms the sequence obtained after 2 h of OCP test, and the Ti/（IrO2-Ta2O5） mesh attains the lowest corrosion current density. The Ti/（IrO2-Ta2O5） mesh anode also shows better performance after 24 h of galvanostatic polarization with the overpotential lower than that of the conventional Pb-Ag anode by about 245 mV.

Hierarchical Co3O4 Microstructures Decorated with Ag and Cu Oxides： Study of Photocatalytic and Electrochemical Properties

Three-dimensional hierarchical Co3O4 microstructures decorated with Ag and Cu oxides were prepared via displacement reaction and subsequent annealing treatment.Photocatalytic properties measurements revealed that the photocatalystic activities of Cu O/Co3O4 composites（Co3O4 microstructures decorated with Cu O）were enhanced while those of Ag2O/Co3O4 composites（Co3O4 microstructures decorated with Ag2O）were reduced,when compared with those of pure hierarchical Co3O4 microstructures toward the degradation of methyl orange.In addition,Cu O/Co3O4 composites exhibited an excellent recyclability ability of photodegradation.The electrochemical properties test indicated that both of the composite oxide electrodes exhibited excellent pseudocapacitive performance with relatively high specific capacitance and good long-term cycling stability.With the increase of the loaded Ag2O and Cu O dosages deposited on the Co3O4 microstructures surface,the specific capacitance values of the composites were increased.Ag2O/Co3O4 composite electrodes showed higher specific capacitance values and better cycling stability than Cu O/Co3O4 composite ones.

Electrochemical evaluation of the inhibitory effects of acetic acid on Saccharomyces cerevisiae

A mediated electrochemical method was proposed for toxic evaluation of acetic acid on S. cerevisiae AS. 380, and menadione/ferricyanide was chosen as the mediator system. The variance in electrochemical response in the absence and presence of increasing concentrations of acetic acid were used to indicate the inhibitory effects of weak acid on the yeast. The inhibitory effects of acetic acid on glucose consumption during menadione mediated reduction of ferricyanide were also measured for comparison purpose. The relative limiting current and the glucose consumption were reduced by 64.5% and 61%, respectively, in the presence of 4g/L acetic acid at pH 4.0. The results showed that the electrochemical method can provide us with an appropriate and convenient tool for cytotoxic evaluation.

Micro/nanoelectrode-based electrochemical methodology for single cell and organelle analysis

Cells are the basic unit of life.Electrochemical analysis of single cells/organelles is essential for uncovering the molecular mechanisms of physiological and pathological processes that are difficult to elucidate on a larger scale.This paper provides an overview of the commonly used fabrication methods for micro/nanoelectrodes applied in the investigations of single cells/organelles as well as the corresponding electrochemical measurements over the last four years including extracellular measurement,combination of extra and intracellular measurement,intracellular reactive oxygen species and reactive nitrogen species(ROS/RNS)measurement,and isolated organelles measurement.

Corrosion behavior of T2 copper in 3.5% sodium chloride solution treated by rotating electromagnetic field

Copper is susceptible to producing corrosion problems in corrosive environments, which leads to serious safety problems. Thus, investigating the corrosion behavior of copper is of great significance. The effects of rotating electromagnetic field on corrosion behavior of T2 copper in 3.5% sodium chloride solution with electrochemical measurements were investigated. The results showed that rotating electromagnetic field changed properties of 3.5% sodium chloride solution by increasing the values of temperature and pH and decreasing the values of conductivity and dissolved oxygen. The rotating electromagnetic field improved the corrosion resistance of T2 copper. The corrosion products of T2 copper in treated 3.5% sodium chloride solution were composed of Cu20 and CuCl. The low corrosion rate of T2 copper was resulted from the decrease of dissolved oxygen in 3.5% sodium chloride solution treated by rotating electromagnetic field.

A comparative corrosion behavior of Mg,AZ31 and AZ91 alloys in 3.5%NaCl solution

The corrosion behavior of Mg,AZ31 and AZ91 has been evaluated in 3.5%NaCl solution using weight loss,electrochemical polarization and impedance measurements.Corrosion rate derived from the weight losses demonstrated the occurrence of steeply fast corrosion reaction on AZ91 alloy after three hours of immersion,indicating the start of galvanic corrosion.An increase of corrosion rate with immersion time was also observed for AZ31 but with lesser extent than AZ91 alloy.Whereas Mg metals showed a decrease of corrosion rate with immersion time,suggesting the formation of a protective layer on their surfaces.In contrast,the corrosion current density(I_(corr))derived from the Tafel plots,exhibited their corrosion resistances in order of Mg>AZ91>AZ31.Electrochemical charge transfer resistance(R_(ct))and double layer capacitance measured by electrochemical impedance spectroscopy(EIS),are well in accordance with the measured I_(corr).EIS measurements with time and microstructural examination of the corroded and uncorroded samples are helpful in elucidation of results measured by electrochemical polarization.

Corrosion behavior of Mg-Zn-Ca amorphous alloys with Nd addition in simulated body fluids

The effects of Nd addition on corrosion behavior of Mg66Zn30Ca4 amorphous alloys in simulated body fluids （SBF） were studied in this paper. Electrochemical properties of the samples before and after corrosion were determined. Surface morphologies of samples after immersion in SBF at 37 ℃ for different times were observed under scanning electron microscope （SEM）. Results show that the corrosion resistance of Mg-based alloys in SBF is improved with the addition of Nd element. The electrochemical properties indicate that microalloying Nd element to the alloys leads to an ennoblement in the open circuit potentials of the alloys and a decrease in the anodic current density in SBF, especially for the Mgee66-xZn30Ca4Ndx alloys with Nd content of 1.0at.%-1.5at.%. It was observed that the surface morphologies of the alloys immersed in SBF change with the Nd addition. A flake- like structure parallel to the alloy substrate formed on the surface of 1.0at.% Nd-containing alloy immersed in SBF for 7 days improves the corrosion resistance of the amorphous alloys by blocking the corrosion liquid from attacking the alloys.

Corrosion Protection of CNTs/CNFs Modified Cement Mortars

The aim of this study is to examine the performance of nano additives in two different sets of mortar specimens armed with reinforcing steel rebars. In particular, three sets of reinforced concrete cylinders with additives of 0.1% wt of carbon nanotubes (CNTs) and carbon nanofibers (CNFs) have been exposed to a solution of 3.5% NaCl, and further examined for the impact of nano-modification on corrosion performance. The anti-corrosive performance of these additives was investigated through linear polarization technique (LPR), mass loss and mercury porosimetry technique (MIP). From the investigation results, it is found that the addition of CNTs/CNFs causes lower steel corrosion, whereas the pore structure of concrete with CNTs/CNFs can significantly reduce the mass loss rate and the relative permeability.

Corrosion Inhibition Studies of Benzoxazole Derivates for N80 Steel in 1 M HCl Solution: Synthesis, Experimental, and DTF Studies

Three benzoxazole corrosion inhibitors, namely 2-(benzo [d]oxazol-2-yl)phenol (BOP), 6-(benzo [d]oxazol-2-yl)pyridin-2-ol (BOPO), and 2-(quinolin-2-yl) benzo [d]oxazole (QBO), were synthesized. Moreover, their corrosion inhibition performance for N80 steel in 1 M HCl solution at 303 K was measured by the electrochemical measurements and surface analysis studies. The results show that the inhibition efficiency of all corrosion inhibitors increases with the increase of concentration. At the same concentration, the order of inhibition efficiency is BOP < BOPO < QBO. Moreover, the studied inhibitors act as mixed-type inhibitors, and the adsorption of all inhibitors on N80 steel followed the Langmuir adsorption isotherm. Further, we have examined the effect of iodide ions on inhibition efficiency. The results show that BOP and KI are synergistic, BOPO and QBO are competitive adsorptions with KI. The quantum chemical parameters such as highest occupied molecular orbital, lowest unoccupied molecular orbital energy levels, and energy gap were calculated by the density functional theory (DTF). The relations between the inhibition efficiency and some quantum parameters have been discussed. The protective effect of the three inhibitors followed the sequence of BOP < BOPO < QBO. The results obtained from quantum chemicals and electrochemical were in reasonable agreement.

Triazole derivatives as corrosion inhibitors for mild steel in hydrochloric acid solution

The title compounds 1-（4,5-dihydro-3-phenyl pyridine-1-yl）-2-（1H-1,2,4-triazole-1-yl） ethyl ketones were studied as a corrosion inhibitor in a mild steel in 1 mol /L hydrochloric acid solution using weight loss measurement, potentiodynamic polarization, and electrochemical impedance spectroscopy （EIS）. Results indicated that these compounds had excellent inhibition properties. Polarization curves indicated that the inhibitor behaved mainly as mixed-type inhibitor. The EIS results showed that the charge transfer controlled the corrosion process in the uninhibited and inhibited solutions. Adsorption of the inhibitor on the mild steel surface followed Langmuir＇s adsorption isotherm with negative value of the free energy of adsorption ΔGads^o. The thermodynamic parameters of adsorption were determined and discussed.

Micro structure and corrosion behavior of ALD AI2O3 film on AZ31 magnesium alloy with different surface roughness

There remains growing interest in magnesium(Mg)and its alloys,as they are the lightest structural metallic materials and potential metallic biomaterials.In spite of the greatest historical Mg usage at present,the wider use of Mg alloys remains restricted by the poor corrosion resistance.A nano amorphous film,as the composition of Al2O3,had now been deposited on the AZ31 Mg alloy substrate by atomic layer deposition(ALD).Grazing incidence X-ray diffraction(GIXRD),X-ray reflectivity(XRR),X-ray photoelectron spectroscopy(XPS),atomic force microscope(AFM)and scanning electron microscopy(SEM)had been employed to identify the chemical compositions,microstructure and Al2O3/Mg interface of specimens firstly.Then corrosion behavior had been evaluated by neutral salt spray test and electrochemical measurement.The results showed that nano amorphous film made a homogeneous cover on Mg alloy.The film could improve the corrosion resistance of Mg alloy greatly,not only with a positive shift in Ecorr and a decrease in icorr,but also with a more uniform corroded mode.Furthermore,the roughness was found to be an important factor for corrosion resistant,in the way that rougher surface was corroded worse,and greater improvement would be in corrosion resistant after nano amorphous film deposition.

Model test of the stability degradation of a prestressed anchored rock slope system in a corrosive environment

The long-term stability of a prestressed anchored slope might be influenced by the durability of the anchorage structure.To understand long-term stability of anchored rock slopes,the research presented herein evaluated the performance evolution of a prestressed anchored bedding slope system in a corrosive environment by model test.The corrosion process in a prestressed anchor bar was monitored in terms of its open-circuit potential(OCP),corrosion current density(CCD),and electrochemical impedance spectroscopy(EIS).The stability of the prestressed anchored slope was evaluated by monitoring changes in anchorage force and displacements.The experimental results show that prestress and oxygen could reduce the corrosion resistance of the anchor bar,and anchor bars in a chloride-rich environment are very susceptible to corrosion.Prestressed tendons in a corrosive environment suffer a loss of anchorage force,the prestress decreases rapidly after locking,and the rate thereof decreases until stabilising;in the later stage,corrosion leads to the reduction of the cross-sectional area of the steel bar which may cause the reduction in anchorage force again.Anchorage force controls the deformation and stability of the anchored slope,the prestress loss caused by later corrosion may lead to an increased rate of displacement and stability degradation of the prestressed anchored rock slope.

Optimization of Cr/Mo molar ratio in FeCoCrMoCBY alloys for high corrosion resistance

The corrosion behavior of bulk metallic glasses(BMGs)(Fe41Co7Cr15Mo14C15B6Y2)100-xCrx(x=0,4,8,12,molar fraction,%)was investigated in1mol/L HCl aqueous solution with electrochemical tests.The electrochemical measurements demonstrate that the passive current density of Fe-based amorphous alloy is reduced by about one order of magnitude,and meanwhile,the stability of passive film can be guaranteed by the Cr/Mo molar ratio.The Mott–Schottky(M–S)curves show that the passive film is the densest when the molar ratio of Cr/Mo is between1.37and1.69.X-ray photoelectron spectroscopy(XPS)analysis was performed to clarify chemical states of elements in the passive films.The results show that the corrosion resistance of the alloy is related to the molar ratio of Cr/Mo.The stability of passive film is determined by the synergistic action of Cr and Mo elements.The main component of the passive film is Cr3+oxide.When the potential is greater than0.5V(vs SCE),Mo6+ions play an important role in keeping the stability of the passive film.The appropriate molar ratio of Cr/Mo can reduce the dissolution rate of the passive film.

2,3,5-Triphenyl-2H-tetrazolium Chloride and 2,4,6-Tri（2-pyridyl）-s-triazine on the Corrosion of Mild Steel in HCl

Electrochemical measurement, quantum chemical method, and scanning electron microscopy （SEM） were performed to investigate the inhibitive effect of 2,3,5-triphenyl-2H-tetrazolium chloride （TTC） and 2,4,6-tri（2-pyridyl） -s-triazine（TPT） on the corrosion of mild steel in lmol.L^-1 HCl at room temperature. Impedance spectroscopy measurement showed that the polarization resistance increased and that double layer capacitance decreased with the increase in the inhibitive concentration, and the results of potentiodynamic polarization showed that the inhibitors suppressed both cathodic and anodic processes of steel corrosion without change in the mecha-nism. Higher the orbital density distribution strength of the lowest unoccupied molecular orbital, higher is the molecule dipole, and lower energy gap between the energy of the highest occupied molecular orbital and the energy of the lowest unoccupied molecular orbital resulted in higher inhibitory efficiency. The results of SEM analysis showed that the metal-was protected from aggressive corrosion by the addition of TTC and TPT.

Stability of [BMIM]HSO_4 for using as additive during zinc electrowinning from acidic sulfate solution

The stability of ionic liquid additive 1-butyl-3-methylimidazolium hydrogen sulfate （[BMIM]HSO4） during zinc electrowinning from acidic sulfate solution was investigated by cyclic voltammetry, electrochemical impedance spectroscopy and scanning electron microscopy. Compared with the traditional industrial additives, gelatine and gum arabic, [BMIM]HSO4 has more excellent chemical and thermal stabilities. The inhibition effects of gelatine and gum arabic on the zinc electrocrystallization are observed to markedly weaken due to their part degradation after 12 h longtime successive electrolysis and high temperature （90 ℃） treatments. In contrast, the activity of [BMIM]HSO4 is practically unaffected after 24 h longtime successive electrolysis and high temperature treatments. These results are corroborated with the corresponding morphological analysis of the cathodic deposits.

Properties of passive nano films on zircaloy-4 affected by defects induced by hydrogen permeation

In this work, hydrogen absorption and the permeation behavior of the passive layer formed on zircaloy-4 are in- vestigated. Potentiodynamic polarization, Mott-Schottky analysis, electrochemical impedance spectroscopy, and Raman scattering spectroscopy are employed to characterize the passive defects before and after hydrogen permeation. It is found that the nanoscale passive ZrO2 films play an important role in the resistance against corrosion; hydrogen impingement, however, reduces the passive impedance towards hydrothermal oxidation. The increase of defects （vacancies） in passive film is probably attributed to the degradation. We believe that this finding will provide valuable insight into the understanding of the corrosion mechanism of zircaloys used in light water reactors.

Influence of Ozone Injection on Corrosion Behavior of Steel in Water Ballast Tank

Ozone is the principal active substances and usually employed in ballast water management systems. In the present study, the corrosion protective effect of ozone was conducted by immersion test and electrochemical techniques. It was found that corrosion protective effect was revealed in the range of 2.0 to 2.7 ppm of ozone concentration in seawater. The ratio of the rust area of specimen became 20% in that concentration region. The rusted area is strongly influenced by the ozone concentration and the flow rate determined by FEM （finite element method）. Ozone has a good influence for ballast tanks, i.e., ozone can delay the rust of ballast tanks, provided that the suitable concentration of ozone is selected. In this case, ozone may stop the corrosion at the defects, if a part of the paint in ballast tank is peeled off. However, ozone may also promote the corrosion of steel when the ozone concentration is very high, e.g., 10 ppm. Attention should be paid to the ozone concentration, if we use ozone as an active substance for ballast water management systems.