Electronic Properties of Passive Films Formed on G3 and G30 Nickel-based Alloys in Bicarbonate/Carbonate Buffer Solution

The electronic properties of passive films formed on G3 and G30 alloys in bicarbonate/carbonate buffer solution were comparatively studied by electrochemical impedance spectra（EIS） and Mott-Schottky analysis, the chemical composition of the passive film formed on G3 alloy was detected by X-ray photoelectron spectroscopy （XPS）. The results show that passive film on G3 alloy had better protection than that on G30 alloy. The transfer resistance, film resistance and diffusion resistance of the passive films on both alloys increased with increasing formation potential, prolonging formation time, increasing pH value, decreasing formation temperature, and decreasing chloride and sulphide ions concentration. Mott-Schottky plot reveals that the passive films on the two alloys show a p-n semi-conductive character. XPS analysis indicates that the passive film on G3 alloy was composed of an inner Cr oxide and an outer Fe, Mo/Ni oxides.

Effect of Cl^- on the Properties of the Passive Films Formed on 316L Stainless Steel in Acidic Solution

The corrosion behavior of 316L stainless steel （31 6L SS） has been investigated in solutions containing various concentrations of chloride ions by using potentiodynamic polarization, capacitance measurement and Mott- Schottky relationship analysis （M-S）. The result indicates that passive currents change slightly with the addition of chloride ions. The pitting potential （Epit） decreases linearly with Iog[CI-]. Correspondingly, the point defect diffusion coefficient （Do） of the passive film increases linearly with increasing Iog[CI-]. The results also indicate that the pitting corrosion of 316L SS follows the adsorption mechanism in NaCI solution.

Electrochemical Behavior of Passive Films Formed on the Surface of Coarse-,Fine-and Ultra-fine-Grained AA1050 Based on a Modified PDM

Electrochemical impedance spectroscopy （EIS） and Mott-Schottky analysis were carried out to evaluate the electrochemical behavior of the passive films formed on the surface of coarse-grained （CG）, fine-grained （FG） and ultrafine-grained （UFG） 1050 A1 alloy （AA1050） samples in alkaline media （pH value of 8.0） based on a modification of point defect model （PDM）. The EIS results revealed that the polarization resistance increased from about 22.71-120.33 kΩ cm2 for UFG sample when compared to CG sample （annealed sample）. The semiconductor properties of the passive films formed on CG, FG and UFG AA1050 samples in the test solution were investigated by employing Mott-Schottky analysis in conjunction with PDM. The results indicated that donor densities were in the range of 2.19 × 1021-0.61 × 1021 cm-3 and decreased with grain refinement. Finally, all electrochemical tests showed that the electrochemical behavior of AA1050 alloy was improved by decreasing the grain size, mainly due to the formation of thicker and less defective oxide films.

Effect of Chloride on Semiconducting Properties of Passive Films Formed on Supermartensitic Stainless Steel in NaHCO_3 Solution

The effects of chloride ion on the electrochemical behavior and the semiconducting properties of the passive film on supermartensitic stainless steel in 0.5 mol/L NaHCO_3 solution were investigated using potentiodynamic polarization, the potentiostatic current transients and Mott-Schottky analysis. The results indicated that chloride ion narrowed passivation region and improved pitting susceptibility. The steady state current densities were independent of film-formed potentials, which was in good agreement with the assumption of the point defect model （PDM）. The capacitance results showed the fact that the passive films had a multilayer character. The defect density decreased with increasing passive film formation potential. The chloride ion induced changes of the acceptor densities and donor densities of the passive films.

Corrosion Resistance and Semiconducting Properties of Passive Films Formed on 00Cr13Ni5Mo2 Supermartensitic Stainless Steel in Cl^- Environment

The semiconducting properties of passive films grown on 00Crl3Ni5Mo2 supermartensitic stainless steel were investigated in comparison with conventional 2Cr13 martensitic stainless steel. Cyclic vohammetry and electro- chemical impedance spectroscopy （EIS） were used for the studies. 00Crl3NiSMo2 steel exhibited a good corrosion resistance performance, attributing to its passive capability. The results of Mott-Schottky analysis demonstrated n- type semiconductors for the passive films with doping densities of about 1020- 1021 cm -3, and the thickness of space- charge layers was also calculated. The experimental results confirmed that Mo plays an important role in improving the corrosion resistance of 00Crl3Ni5Mo2 steel due to its impact on the doping density.

Electrochemical Hydrogen Charging on Corrosion Behavior of Ti-6Al-4V Alloy in Artificial Seawater

This study employs advanced electrochemical and surface characterization techniques to investigate the impact of electrochemical hydrogen charging on the corrosion behavior and surface film of the Ti-6Al-4V alloy.The findings revealed the formation ofγ-TiH andδ-TiH_(2) hydrides in the alloy after hydrogen charging.Prolonging hydrogen charging resulted in more significant degradation of the alloy microstructure,leading to deteriorated protectiveness of the surface film.This trend was further confirmed by the electrochemical measurements,which showed that the corrosion resistance of the alloy progressively worsened as the hydrogen charging time was increased.Consequently,this work provides valuable insights into the mechanisms underlying the corrosion of Ti-6Al-4V alloy under hydrogen charging conditions.

Study on the passive film formed on 2205 stainless steel in acetic acid by AAS and XPS

The properties of the passive film formed on 2205 stainless steel in acetic acid at high temperature that contained chloride ions were studied by atomic absorption spectrometry （AAS）, X-ray photoelectron spectroscopy （XPS）, and electrochemical polarization measurements. AAS results show that molybdenum is enriched on the surface as the passive film is dissolved. This enrichment decreases the corrosion resistance because it hinders chloride adsorption and Fe ion dissolution, and acts as a local pH buffer because it consumes protons. The dissolution ratio of Fe/Cr is approximately 10 during the active dissolution of the passive film. XPS results indicate that when the potential is in the passivation region, Cr comprises about 50% of the metal cations in the near-surface region of the passive film and is the main metal constituent in this region. When the polarization potential is much greater than the transpassivation potential, the Mo content accounts for approximately 45% of the metal cations in the nearurface region; Fe and Ni have no obvious influence on the formation, dissolution, or puncture of the passive film.

Effect of microstructure and passive film on corrosion resistance of 2507 super duplex stainless steel prepared by different cooling methods in simulated marine environment

The effect of microstructure and passive film on the corrosion resistance of 2507 super duplex stainless steel(SDSS)in simulated marine environment was investigated by electrochemical measurements,periodic wet–dry cyclic corrosion test,scanning Kelvin probe force microscopy,atomic force microscopy,and X-ray photoelectron spectrometry.The results show that the occupation ratio ofγphase increases with the decrease in cooling rate,whereas the content ofαphase reduces gradually.In addition,theσprecipitated phase only emerges in the annealed steel.The pitting sensitivity and corrosion rate of 2507 SDSS reduce first and then increase as the cooling rate decreases.Theσprecipitated phase drastically reduces the protective ability of the passive film and facilitates micro-galvanic corrosion of the annealed steel.For various microstructures,the pits are preferentially distributed within theσandγphases.The corrosion resistance of 2507 SDSS prepared by different cooling methods is closely related to the microstructure and structure(stability and homogeneity)of the passive film.Normalized steel shows an optimal corrosion resistance,followed by the quenched and annealed steels.

Investigation of the passive behaviour of AZ31B alloy in alkaline solutions

In this work,the passivity of AZ31B alloy in NaOH solutions was studied by potentiodynamic polarization,electrochemical impedance spectroscopy(EIS)and Mott-Schottky analysis.Potentiodynamic polarization results indicated that decreasing NaOH concentration leads to decrease the corrosion rate of this alloy.EIS results showed that the reciprocal capacitance(1/C)of the passive film is directly proportional to its thickness which increases with decreasing NaOH concentration.Therefore,it is clear that dilute NaOH solutions offer better conditions for forming the passive films with higher protection behaviour,due to the growth of a much thicker and less defective films.The Mott-Schottky analysis revealed that the passive films displayed n-type semiconductive characteristics,where the oxygen vacancies and interstitials(over the cation vacancies)preponderated.Also,Mott-Schottky results showed that the donor densities evaluated from Mott-Schottky plots are in the range of 10^(20) cm^(−3) and decreased with decreasing NaOH concentration.

XPS analysis of passive film formed on the G3 nickel-base alloy tubing under corrosive conditions

In the present study, the passive film formed on the G3 nickel-base alloy tubing under corrosive conditions including H2S ,CO2 ,and Cl-at 130 ℃ and 205 ℃ is studied with X-ray photoelectron spectroscopy（XPS）. The results reveal that the passive film formed at 205℃ consists of Cr, Ni, Fe, S and O elements and is over 470 nm in thickness. The passive film can be divided into three layers, the outer-layer is composed of NiS2 and Cr2 S3 , the intermediate-layer of Cr（OH） 3, Ni （OH） 2, NiS2, Cr2 $3 and a small quantity of NiO and Cr2 O3, and the inner-layer of NiO, Cr2 O3, and alloy elements. Due to the invasion of S2 - into the passive film and the decrease of the content of chromium oxide in the film, the corrosion resistance of the G3 alloy in the sour environment at 205 ℃ is weakened.

STUDIES OF LOW-CONCENTRATION CHROMATE PASSIVE FILM FOR ZINC-BASED ALLOY COATED STEEL WIRES

The corrosion resistance of a low concentration chromate passive film for zinc based alloy coated steel wires was assessed by salt spray and electrochemical corrosion tests. XPS and AES analyses showed that the composition of such chromate passive film was S 5 5, Na 3 4, C 11 8, Ti 7 9, O 41 6, Cr 13 7, Zn 16 0.

ELECTRON ENERGY SPECTRUM ANALYSIS ON PASSIVE FILM OF Si-BEARING STAINLESS STEELS

The surface films on the Si-bearing stainless steels formed after soaking in the concentrated nitric acid for 216 h have been investigated by means of an electron energy spectrometer.It can he reached that Si builds up in the surface in the form of SiO_2.It plays a main part as a passivating element in the Si-bearing stainless steels in strong oxidizing medium,whereas Cr drops down to the second place.

Influence of second phase precipitates on mechanical and in-vitro corrosion behaviour of Mg-4Zn-0.5Ca-0.8Mn alloy in optimum homogenized conditions

The present study investigates the mechanical and in-vitro corrosion behavior of Mg-4Zn-0.5Ca-0.8Mn alloy in optimum homogenized conditions.The optimization of the homogenization parameters has been carried out employing thermodynamic calculations and kinetic modeling.The model utilizes the inter-diffusivity of the solute elements and predicts that∼6–24 h of homogenization at 633 K effectively redistributes the elements in the Mg matrix.Based on the insights obtained from the simulations,the as-cast Mg-4Zn-0.5Ca-0.8Mn alloy was subjected to homogenization heat treatment process for 6–24h.The microstructural study through optical microscopy and scanning electron microscopy(SEM)revealed that the interconnected network of second phase precipitates substantially dissolve within 24 h,implying adequate homogenization.Moreover,fine Mg-Zn based precipitates with varied morphology and phase fractions also evolved during homogenization treatment,as confirmed through SEM and transmission electron microscopy.In the 12 h homogenized specimen,the highest fraction of uniformly dispersed fine precipitates resulted in the highest strength(∼225 MPa).On the other hand,a substantial disruption in coarse precipitate network and lower aspect ratio of fine Mg-Zn precipitates led to the highest ductility(∼8%)in this specimen.In the 24 h homogenized specimen,the ductility reduced marginally owing to higher aspect ratio of fine precipitates.The immersion and electrochemical tests(viz.,potentiodynamic polarization and electrochemical impedance spectroscopy)carried out in Hank’s solution revealed that the 24 h homogenized specimen exhibits the best corrosion properties.The least fraction of Ca_(2)Mg_(6)Zn_(3)phase with maximum disruption in interconnectivity,in combination with a small fraction of fine equilibrium MgZn_(2)precipitates,resulted in suppression of localized corrosion in this specimen.This promotes the formation of the most stable and compact product layer over the specimen,resulting in the highest corrosion resistance.

Inhibition mechanism of air nanobubbles on brass corrosion in circulating cooling water systems

Air nanobubbles(A-NBs)were used to inhibit the brass corrosion in circulating cooling water for the first time in the study.The results of mass loss method and electrochemical method showed that A-NBs had the obvious corrosion inhibition effect.The inhibition rate reached 52%at 35℃.The impedance and surface characterization results of corrosion samples indicated that the corrosion inhibition mechanisms of A-NBs mainly included adsorption of corrosion ions,promoting the formation of the passivation film on metal surface and the formation of the bubble layer and scale film on metal surface.A-NBs are potential excellent corrosion inhibitors.

Stress corrosion cracking of X80 pipeline steel exposed to high pH solutions with different concentrations of bicarbonate

Susceptibilities to stress corrosion cracking （SCC） of X80 pipeline steel in high pH solutions with various concentrations of HC03 at a passive potential of-0.2 V vs. SCE were investigated by slow strain rate tensile （SSRT） test. The SCC mechanism and the effect of HC03 were discussed with the aid of electrochemical techniques. It is indicated that X80 steel shows enhunced susceptibility to SCC with the concentration of HCO3 increasing from 0.15 to 1.00 mol/L, and the susceptibility can be evaluated in terms of current density at -0.2 V vs. SCE. The SCC behavior is controlled by the dissolution-based mechanism in these circumstances. Increasing the concentration of HCO3 not only increases the risk of rupture of passive films but also promotes the anodic dissolution of crack tips. Besides, little susceptibility to SCC is found in dilute solution containing 0.05 mol/L HCO3 for X80 steel. This can be attributed to the inhibited repassivation of passive films, manifesting as a more intensive dissolution in the non-crack tip areas than at the crack tips.

Effects of HNO_3 concentration on the pit morphologies of aluminum foil etched in HNO_3–HCl and HNO_3–H_2SO_4–HCl solutions

In this work, the effects of HNO3 concentration on the pit morphologies of high-cubic-texture aluminum foil etched in HNO3-HCl and HNO3-H2SO4-HCl solutions were investigated. When the aluminum foil was etched in HNO3-HCl solutions, the morphologies of pits transformed from irregular tunnels to typical tunnels （as inverted pyramids） and shallow cuboids as the HNO3 concentration in the etchant solution was increased. However, as the HCl concentration in the etchant solution was increased, the morphologies of pits transformed from shallow cuboids to typical tunnels （as inverted pyramids） and irregular tunnels. When the aluminum foil was etched in n N HNO3-（7.2-n） N H2SO4-0.8 N HCl solutions, the morphologies of the pits transformed from typical tunnels （i.e., the number of sub-tunnels formed on the main tunnels increased） to irregular tunnels （corrugated tnnnels and polyline tunnels） as the HNO3 concentration in the etchant solution was increased. These effects are attributed primarily to corrosion on the （100） and （010） faces of pits being accelerated and to the （001） faces be- ing prone to passivation to different degrees when various concentrations of HNO3 are added to the etchant solutions.

Degradation Behavior of Ti-6Al-4V Alloys for Dental Applications in Acidic Artificial Saliva Containing Fluoride Ion

The aim of this work was to study the degradation behavior of Ti-6Al-4V alloys for dental applications in acidic artificial saliva with fluoride ion using electrochemical techniques, optical microscopy, scanning electron microscopy（SEM）, and energy dispersive spectrometry（EDS）. The experimental results showed that fluoride ion had significant influence on the degradation of Ti-6Al-4V alloys, and there was an obvious critical concentration of fluoride ion（about 0.1wt%）. With increasing fluoride ion concentration, the corrosion potential（Ecorr） of alloys moved toward negative and the impedance of alloys decreased, meanwhile, noticeable transformation from minimum corrosion to severe pitting corrosion was observed on alloys surface following the dissolution of TiO2 passive films, leading to the decrease of the corrosion resistance of alloys. The electrochemical dissolution of TiO2 passive films involved a nucleophilic attack of fluoride atom to the titanium atom of TiO2. In addition, Ca^（2＋）and Na~＋ in acidic saliva may involve the surface reactions and make the reactions more complex.

Intergranular corrosion behavior of high nitrogen austenitic stainless steel

The intergranular corrosion （IGC） behavior of high nitrogen austenitic stainless steel （HNSS） sensitization treated at 650-950℃ was investigated by the double loop electrochemical potentiodynamic reactivation （DL-EPR） method. The effects of the electrolytes, scan rate, sensitizing temperature on the susceptibility to IGC of HNSS were examined. The results show that the addi-tion of NaCl is an effective way to improve the formation of the cracking of a passive film in chromium-depleted zones during the reactivation scan. Decreasing the scan rate exhibits an obvious effect on the breakdown of the passive film. A solution with 2 mol/L H2SO4＋1 mol/L NaCl＋0.01 mol/L KSCN is suitable to check the susceptibility to IGC of HNSS at a sensitizing temperature of 650-950℃ at a suitable scan rate of 1.667 mV/s. Chromium depletion of HNSS is attributed to the precipitation of Cr2N which results in the susceptibility to IGC. The synergistic effect of Mo and N is suggested to play an important role in stabilizing the passive film to prevent the attack of IGC.

Grain refinement of bronze alloy by equal-channel angular pressing(ECAP) and its effect on corrosion behaviour

The corrosion behaviour of bronze alloy prepared by equal channel angular pressing(ECAP) was investigated in 3.5 wt. % Na Cl solution.Immersion corrosion tests and different electrochemical techniques were carried out. The results showed that ECAPed bronze samples exhibited higher corrosion resistance compared with the as-cast alloy and the passive current density decreased with increasing number of passes. Moreover,the morphology of alloys indicated that the corrosion damage on the surface of ECAPed bronze was smooth and uniform while the as-cast alloy suffered from selective corrosion.

Effect of ultrasonic vibration on the dechromisation corrosion of a CuCr alloy in HCl solution

The effect of ultrasonic vibration on the dechromisation corrosion of a CuCr alloy in HC1 solution was studied and the corrosion mechanisms were analyzed. It is found that ultlasonic vibration reduces the dechromisation incubation time, accelerates the dechromisafion corrosion rate, decreases the temperature and concentration of HC1 solution, and when the dechromisation occurs it seriously weakens the microstmcture of dechromisation layer. It is concluded that ultrasonic vibration can accelerate destruction of the passivation film on the Cr surface and increase the activities of Cl^- and Cr.