Chromium–palladium films on 316L stainless steel by pulse electrodeposition and their corrosion resistance in hot sulfuric acid solutions

Chromium–palladium alloy films with good adhesive strength and higher micro-hardness have been deposited on 316L stainless steel by pulse electroplating. The films are composed mainly of chromium and palladium crystallites in the metallic state, with grain sizes less than 100 nm. On the film surface Cr(OH)₃ and Cr₂O₃ are present. The co-deposited Cr and Pd in the films show a synergetic effect on passivation. In boiling 20 wt.% H₂SO₄ solution, boiling acetic–formic acid mixture, and simulated PEM fuel cells environment, the Cr–Pd-plated 316L steel shows excellent corrosion resistance.     

The electroplated palladium-copper alloy film on 316L stainless steel and its corrosion resistance in mixture of acetic and formic acids

Palladium-copper alloy films (Cu 2.93-5.66 at.%) were deposited on 316L stainless steel by electroplating. The films showed good adhesive strength and increased surface micro-hardness. In boiling mixture of 90% acetic acid + 10% formic acid + 400 ppm Br⁻ under stirring (625 r/min), the Pd-Cu films showed better corrosion resistance than Pd film. The Pd-5.66%Cu films showed the lowest corrosion rate almost three orders of magnitude lower than that of 316L matrix. The increased corrosion resistance of Pd-Cu films was attributed to the improved passivity, better barrier effect, increased surface hardness and the effect of Cu to resist pitting.     

Electrodeposition of polypyrrole on 316L stainless steel for corrosion prevention

The electrosynthesis of polypyrrole films onto 316L stainless steel from near neutral and alkaline solutions containing molybdate and nitrate is reported. The corrosion behavior of the coated electrodes was investigated in NaCl solutions by electrochemical techniques and scanning electron microscopy. The polymer formed potentiostatically in a solution of pH 12 is the most efficient in terms of adhesion and corrosion protection. The coating significantly reduces the pitting corrosion of the substrate. The results are interpreted in terms of the nature of dopants, the good electroactivity of the polymer formed in alkaline solution and the passivating properties of the oxide layer.     

316L不锈钢上电刷镀钯膜的组成与耐蚀性(英文)

利用电刷镀工艺在316L不锈钢上制备了结合力良好的钯膜。使用扫描电子显微镜、X射线能谱、X射线光电子能谱(XPS)、质量损失实验和电化学测试研究了膜层的性能。结果表明,电刷镀钯膜主要是由钯元素构成的;XPS分析表明,膜层中的钯为金属态。电刷镀钯后的不锈钢试样在沸腾的20%硫酸溶液和含0.005mol/L溴离子的甲酸和乙酸混合溶液中均显示了非常好的耐蚀性能。镀钯试样的腐蚀速率比不锈钢试样的下降了2个数量级。     

Microstructure and pitting corrosion resistance of annealed duplex stainless steel

The transition from metastable to stable pitting was studied in 0.5 M NaCl water solution for two cast duplex stainless steels under different microstructural conditions achieved by annealing in the range from 900 °C to 1200 °C. The ensuing microstructural changes in heat treated steels were defined and correlated with established pitting potentials (E_p) and sites of corrosion damage initiation. The variations in E_p have been discussed in terms of secondary phases precipitation. The critical condition for pit stability was quantified and used to select an appropriate microstructural state, resulting in the higher potential at which stable pit growth is first observed.     

Investigation of intergranular corrosion of 316L stainless steel diffusion bonded joint by electrochemical potentiokinetic reactivation

Electrochemical potentiokinetic reactivation technique (EPR) was employed to assess degree of sensitization in 316L stainless steel diffusion bonded joint (DBJ). The result showed the degree of sensitization of DBJ was much smaller than that of base material (BM). No chromium carbides precipitated at grain boundaries in DBJ after 100 h treatment at 650 °C, while chromium carbides could be seen clearly in the BM after 8 h treatment, indicating that DBJ has better intergranular corrosion resistance than BM. Diffusion bonding technique will not increase intergranular corrosion susceptibility of 316L DBJ. Reactivation potential has the biggest effect on sensitization.     

A comparative H2S corrosion study of 304L and 316L stainless steels in acidic media

H₂S corrosion of 304L and 316L in oxygen-free Na₂SO₄ + Na₂S solution at pH 3 and temperature of 60 °C were investigated by EIS, potentiodynamic polarisation, multi-component Pourbaix diagrams and microstructure characterization. At similar conditions, lower corrosion rate was observed on 316L, attributed to its denser (1.5 times) and smoother (6%) surface layer and confirmed by SEM micrograph. During polarisation, H₂S increases significantly the critical current density on 304L and passivation current density, i_p, on 316L. Higher i_p on 316L was associated to simultaneous FeS₂–MoS₂ preservation, confirmed by XRD examination. H₂S could have an inhibiting effect on 304L in passivity region.     

Effect of nickel alloying on crevice corrosion resistance of stainless steels

The crevice corrosion behaviour of stainless steels containing 25 mass% Cr, 3 mass% Mo and various amounts of Ni was investigated in natural seawater. The results showed that ferritic steels containing nickel were more resistant to corrosion than both ferritic steels without nickel and austenitic steels. The superiority of the Ni bearing ferritic steel over the other steels was in close agreement with the depassivation pH of those steels in acidic chloride solutions. The results showed that the addition of Ni to ferritic steel was effective in decreasing the depassivation pH and the dissolution rate in acidic chloride solutions at crevices.     

Effect of metallurgical variables on the stress corrosion crack growth behaviour of AISI type 316LN stainless steel

Mill-annealed AISI type 316LN stainless steels, received from two different sources (one indigenous (SS-2) and the other foreign (SS-1)), were tested for stress corrosion cracking (SCC) resistance in a boiling acidified environment of NaCl. SCC results indicated a remarkably lower value of plateau crack growth rate (PCGR) and higher values of K_ISCC and J_ISCC for SS-2, which was attributed to the lower effective grain boundary energy resulting from a higher amount of copper in it. Cold working reduced K_ISCC and PCGR; while thermal aging and welding decreased K_ISCC and increased PCGR vis-à-vis the annealed material.     

Corrosion characteristics of polyaniline-coated 316L stainless steel in sulphuric acid containing fluoride

The corrosion resistance of conducting polyaniline (PANi) coatings deposited on 316L stainless steel (316L SS) at various cycle numbers of cyclic voltammetry (2-, 3- and 4-cycles) by electro-polymerization in sulphuric acid solution containing fluoride was investigated by electrochemical techniques. The corrosion resistance of the 316L SS substrate was considerably improved by the PANi coating. The increase of the cycle number of cyclic voltammetry increased the thickness and enhanced the performance of the PANi coating due to low porosity.     

The role of alkaline-earth additives on the molten carbonate corrosion of 316L stainless steel

The corrosion behavior of 316L stainless steel in eutectic Li/Na molten carbonate containing various amounts of Mg, Ca and Ba ions has been evaluated by electrochemical techniques in combination with oxygen solubility determinations. Open circuit potential and corrosion rates have been correlated to the oxygen solubility properties of the carbonate melt for an understanding of the kinetic aspects of the corrosion process. It has been found that minor additions of Mg and Ca ions (1.5% molar fraction) distinctly promote a higher carbonate oxygen solubility, whereas Ba has only a marginal effect on it. In general, the electrochemical investigations showed that at 1.5% molar fraction addition there exist a strong correlation between steel corrosion rate and oxygen solubility indicating that (i) corrosion process takes place under a diffusion-limited cathodic reduction of dissolved O₂ and (ii) corrosion rate is significantly increased with respect to the no-added Li/Na carbonate by the introduction of Mg and Ca ions that therefore serve as a sort of oxidizing agents. However, with larger Mg and Ca additions (up to 10% mol) the corrosion process was found to pass progressively under an anodic control despite decreasing oxygen solubility values. This effect is ascribed to the growth of an alkaline-earth doped lithium ferrite layer with enhanced barrier-like properties. In contrast, further additions of Ba cation in carbonate did not change the corrosion mechanism for its inability to react with the growing corrosion scale. Only minor reductions of corrosion rate are detected in agreement with the lower tendency of the melt containing high molar fractions of Ba to solubilize the oxygen gas.     

An experimental study of crevice corrosion behaviour of 316L stainless steel in artificial seawater

The effects of applied torque on corrosion behaviour of 316L stainless steel with crevices were investigated using the cyclic potentiodynamic polarization method. Three kinds of crevices (316L-to-polytetrafluoroethylene, 316L-to-fluoroelastomeric and 316L-to-316L) were tested in artificial seawater at 50 °C. Corroded surface morphology was also investigated using scanning electron microscopy. Results indicate similar trends in crevice corrosion susceptibility with increasing applied torque. Among the three crevices, the 316L stainless steel specimen, coupled to the 316L stainless steel crevice former, is the most susceptible to crevice corrosion.     

Numerical simulations study of the localized corrosion resistance of AISI 316L stainless steel and pure titanium in a simulated body fluid environment

The resistance of both AISI 316L stainless steel (AISI 316L SS) and commercially pure titanium (cpTi) to localized corrosion in a simulated body fluid solution was investigated using numerical simulations. The resulting model, based on transport equations in dilute solutions, is designed to predict the susceptibility of these two biomaterials to crevice corrosion initiation. The results show that cpTi and AISI 316L SS alloy are very resistant to the initiation of crevice corrosion in 0.9% NaCl solution and AISI 316L SS alloy is more susceptible to corrosion initiation over the long term than cpTi.     

Effect of annealing temperature on the corrosion behavior of duplex stainless steel studied by in situ techniques

The effects of the annealing temperature on the microstructure and the corrosion behavior of duplex stainless steel 2507 were investigated by means of magnetic force microscopy (MFM), scanning Kelvin probe force microscopy (SKPFM), atomic force microscopy (AFM) and scanning electron microscopy (SEM). The SEM results indicated that the volume fraction of the austenite phase decreased with the increased annealing temperature. SKPFM/MFM measurements conducted in air at the room temperature and an ambient relative humidity of about 25% showed a higher Volta potential of the paramagnetic austenite than that of the ferromagnetic ferrite. The in situ AFM observation in a hydrochloric acid solution provided solid evidence that corrosion preferentially occurred in the ferrite phase. The sample annealed at 1100 °C exhibited a greater Volta potential difference between the ferrite and austenite and a higher corrosion rate in the ferrite, while that annealed at 1150 °C had a smaller Volta potential difference and a lower corrosion rate. The relative nobility and microstructure change of two phases, as well as their corrosion behavior, can be explained by the effect of the composition of alloying elements.     

Acoustic emission during pitting corrosion of 304 stainless steel

Acoustic emission (AE) during pitting corrosion of 304 stainless steel (304 SS) in H₂SO₄ solutions with different pH values and Cl⁻ concentrations was studied. Two types of AE signals are detected in all solutions. Each type of signals is characterized by AE parameters (rise time, counts number, duration and amplitude) and waveform carefully. It is believed that the hydrogen bubbles evolution inside the pits is the AE source.     

Microstructural evolution and localized corrosion resistance of an aged superduplex stainless steel

The present investigation was undertaken to analyze the effects of isothermal ageing treatments, carried out between 700 and 900 °C for a variety of times up to two weeks and followed by water quenching, on the microstructure and on the localized corrosion resistance of a superduplex stainless steel, SAF 2507.The quantitative metallography coupled with X-ray diffraction techniques was adopted to follow the microstructural evolution, together with SEM microscopy.Electrochemical potentiodynamic tests, as cyclic polarization curves recorded in sodium chloride solutions, together with weight loss measurements were employed to evaluate the susceptibility of the aged specimens to pitting corrosion.The influence of the transformation of ferrite into secondary austenite and sigma phase and of other microstructural variations, as chromium nitrides precipitation, on the stability of the passive film is shown. The susceptibility of the aged alloy to pitting corrosion phenomena, is related to sigma phase precipitation in association to the secondary austenite formation, which lead to a noticeable Cr depletion at grain boundaries.     

Environmental factors affecting pitting corrosion of type 304 stainless steel investigated by electrochemical noise measurements under potentiostatic control

Electrochemical noise measurements on anodically polarised type 304 stainless steel surfaces in contact with buffer solutions of neutral pH were performed to study the effect of chloride ions in the nucleation of pitting corrosion. Passive layer stability and susceptibility to pitting corrosion after pickling and passivation at different environmental conditions were also investigated by means of electrochemical current noise measurements under cathodic and anodic polarisation. According to the obtained experimental results pits nucleate independently on the presence of chloride ions. It has been also shown that protectiveness of stainless steel surfaces after pickling strongly depends on the relative humidity of the environment in which the surface is subsequently passivated.     

Protective properties of hexacyanoferrate containing polypyrrole films on stainless steel

The protective properties of polypyrrole coatings containing hexacyanoferrate anions are presented. The composite coatings were electrodeposited galvanostatically on stainless steel from the aqueous solutions containing pyrrole monomer and potassium hexacyanoferrate(II) together with traces (10 μmol dm⁻³) of free CN⁻ ions. The protective properties of the resulting coatings were investigated in the highly aggressive medium of 0.1 mol dm⁻³ HCl and 0.4 mol dm⁻³ NaCl. Diagnostic experiments included measurements of open circuit potential with time of exposure, chronoamperometric (current-time) examination of the steel samples at a selected constant potential of 0.5 V and potentiodynamic measurements. To get insight into the dynamics of the steel dissolution at open circuit potential and at the selected anodic potential, changes of concentrations of iron and chromium in the test solution as a function of exposure time were determined using atomic absorption spectrometry. Morphology of the composite film was examined using scanning electron microscopy.     

Silane–parylene coating for improving corrosion resistance of stainless steel 316L implant material

The corrosion resistance of a two-layer polymer (silane + parylene) coating, on implant stainless steel was investigated by microscopic observations and electrochemical measurements. Long term exposure tests in Hanks solution revealed that the coating of 2 μm can be successfully used for corrosion protection. However, the addition of H₂O₂, simulating the inflammatory response of human body environment causes a dramatic destruction of the protective coating. Analysis of the experimental data in terms of circuit models enables proposing a deterioration mechanism. OH radicals formed at the metal surface attack the polymer, thus the deterioration starts from the metal/polymer interface and progress towards the outward surface.     

Fabrication of continuous mesoporous organic–inorganic nanocomposite films for corrosion protection of stainless steel in PEM fuel cells

The organic–inorganic composite film was deposited on the 304 stainless steel as bipolar plate material for proton exchange membrane fuel cells by spin-coating method. As shown by XRD, N₂ adsorption–desorption and TEM, the composite films exhibit ordered mesoporous structures. The corrosion tests in 0.5 M H₂SO₄ system displayed that, compared with 304SS, the composite films made corrosion potential shifted to positive direction by 250–1000 mV (SCE) and corrosion current decreased by 1–3 orders of magnitude. Wherein, the C-50–60% composite film showed the optimal protective performance, its corresponding potentiostatic polarization process was extremely stable in the simulated fuel cells environment.