Fabrication and anti-corrosion performance of superhydrophobic silane film on sintered NdFeB

An eco-friendly superhydrophobic protective film(DTMS/TEOS silane film)was fabricated on sintered NdFeB substrate through the utilization of electrochemically assisted deposition technology.The structure,properties,and film-forming mechanism of dodecyltrime-thoxysilane(DTMS)/tetraethoxysilane(TEOS)silane films were comprehensively analyzed using Fourier transform infrared spectroscopy(FT-IR),scanning electron microscopy(SEM),X-ray photoelectron spectroscopy(XPS),potentiodynamic polarization curves and electrochemical impedance spectroscopy(EIS).Based on the test results,it can be determined that this film has a superhydrophobic property with a hydrophobicity angle of 152°.This special property can be attributed to the long alkyl chains in the DTMS molecule,the rough morphology,and the low surface energy of the DTMS/TEOS silane film.The surface of sintered NdFeB is coated with a layered three-dimensional network silane film that forms through the condensation of silanol substances.This film provides excellent corrosion resistance to the sintered NdFeB substrate,reducing its corrosion current density to 2.02×10~(-6)A/cm~2.Moreover,the impact of film on the magnetic characteristics of sintered NdFeB was assessed and found to be minimal.

Corrosion resistance of in-situ Mg-Al hydrotalcite conversion film on AZ31 magnesium alloy by one-step formation

In situ growth of nano-sized layered double hydroxides （LDH） conversion film on AZ31 alloy was synthesized by a urea hydrolysis method. The formation mechanism of the film was proposed. Firstly, the dissolved Mg2＋ ions deposited into a precursor film consisted of MgCO3 and Mgs（CO3）4（OH）2·4H2O; secondly, the precursor translated into the crystalline Mg（OH）2 in alkaline conditions; finally, the Mg2＋ ions in Mg（OH）z were replaced by A13＋ ions, Mg（OH）2 translated into the more stable LDH structure, simultaneously, the OH- ions in the interlayer were exchanged by CO32-, thus led to the formation of the LDH （Mg6Alz（OHh6CO3·4H2O） film. The results indicated that the LDH film characterized by interlocking plate-like nanostructures and ion-exchange ability significantly improved the corrosion resistance of the AZ31 Mg alloy.

Effects of boric acid on microstructure and corrosion resistance of boric/sulfuric acid anodic film on 7050 aluminum alloy

The microstructure and corrosion resistance of different boric/sulfuric acid anodic（BSAA） films on 7050 aluminum alloy were studied by atomic force microscopy（AFM）,electrochemical impedance spectroscopy（EIS） and scanning Kelvin probe（SKP）.The results show that boric acid does not change the structure of barrier layer of anodic film,but will significantly affect the structure of porous layer,consequently affect the corrosion resistance of anodic film.As the content of boric acid in electrolyte increases from 0 to 8 g/L,the resistance of porous layer（Rp） of BSAA film increases,the capacitance of porous layer（CPEp） decreases,the surface potential moves positively,the pore size lessens,and the corrosion resistance improves.However,the Rp,CPEp and surface potential will change towards opposite direction when the content of boric acid is over 8 g/L.

Phosphate film free of chromate, fluoride and nitrite on AZ31 magnesium alloy and its corrosion resistance

A phosphate solution free of chromate, fluoride and nitrite was prepared and an environment-friendly film was obtained on AZ31 magnesium alloy surface via the chemical deposition method. The morphology, composition, phase structure and its corrosion resistance were studied. The effects of film-forming temperature and free acid on corrosion resistance, microstructure and electrochemical behavior of the film were discussed. The results indicate that the corrosion resistance of AZ31 with the phosphate film was better than blank AZ31 substrate, which was most attributed to the great inhibitive action on the anodic dissolution and cathodic hydrogen evolution of the film.

Effect of bias voltage on compositional, mechanical and corrosion property of ZrNbAlN multilayer films by unbalanced magnetron sputtering

Nano-scaled ZrNbAlN films with different negative bias voltages（Vb） were deposited on bronze substrate and Si（100） wafers by a reactive unbalanced magnetron sputtering technique. Composition and structure properties were characterized by X-ray photoelectron spectroscopy and X-ray diffraction. It is found that mole concentrations of Zr and Nb are affected by Vb, which leads to the increase of binding energy of N 1s and Al 2p and decrease of binding energy of Zr 3d5/2 and Nb 3d5/2. Surface morphologies evolution controlled by Vb could be observed. Furthermore, X-ray diffraction patterns reveal that these films show a（111） preferred orientation. Moreover, mechanical property and corrosion behavior of ZrNbAlN films were characterized by nanoindentation test and corrosion test, respectively. A maximum value of 21.85 GPa at-70 V occurs in the ZrNbAlN- bronze system, which outperforms uncoated bronze. Corrosion experiments in 0.5 mol/L NaCl and 0.5 mol/L HCl solution show that corrosion potential and corrosion current are dependent on Vb, and better anti-corrosion property could be obtained at-90 V.

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.

Growth and corrosion behavior of rare earth film on hot-dip galvanized steel

Hot-dip galvanized(HDG)steel sheets were treated for 30 s?24 h by the rare earth aqueous solution containing 20 g/L Ce(NO3)3·6H2O,and the growth behavior and corrosion resistance of the rare earth film were investigated by SEM,EDS,AES and NSS.The results reveal that the rare earth film becomes thick while the mass gain of the samples does not distinctly change due to the zinc dissolution with the increase of treatment time.The film grows up more quickly and is apt to cracking in the vicinity of zinc grain boundaries,and eventually the film partly warps and flakes off with increasing film thickness.The NSS results show that the corrosion resistance of the film is dominated by both the film thickness and the cracks.With increasing treatment time,the corrosion resistance of the film increases within 1 h due to the increased film thickness and decreases after 1 h because the cracking and flaking off gradually become dominant factor.

Magnetic performance and corrosion resistance of electroless plating CoWP film

The CoWP film with good magnetic performance and corrosion resistance was electrolessly plated from alkaline solution. The technical parameters of the electroless plating system were optimized. When the pH value of electroless plating solution was 11.0 and the reducing agent (NaH2PO2) content was 0.4 mol L 1, the target chemical reactions proceeded in the electroless plating solution smoothly with negligible interference and side effects. CoWP film prepared under optimal deposition condition contained more hexagonal close-packed (hcp) cobalt (ε-Co) of [110] and crystallographic orientation of Co [002]. VSM analysis reveals that the saturation magnetization of the CoWP film is 100～220 Am2 kg 1 and coercivity is (2.87～4.38)×104 A·cm 1. The corrosion behavior of CoWP film in 3.5% NaCl aqueous solution was studied by electrochemical experiments. The results prove that the corrosion resistance of the CoWP film deposited under the optimal depo-sition condition exhibites relatively lower corrosion current of (3.054～3.162)×10 6 A·cm 2. The surface morphology analysis indicates that the film is smooth and composed of regular-shaped crystallites.

Corrosion protection properties of vanadium films formed on zinc surfaces

Vanadium films were prepared on zinc surfaces by using a solution containing vanadate. Corrosion protection properties of vanadium-treated （V-treated）, chromium-treated （Cr-treated）, and untreated zinc surfaces in contact with a 3.5 wt.% NaC1 solution were studied using potentiodynamic polarization, electrochemical impedance spectroscopy （EIS）, and neutral salt spray （NSS） tests. According to these results, the V-treated layer significantly improved the corrosion resistance of zinc surfaces. In comparison with the Cr-treated layer, the V-treated layer exhibited a better corrosion resistance. The composition of the V-treated layer was studied using X-ray photoelectron spectroscopy （XPS）. XPS measurements indicated that the vanadium layer formed on zinc surfaces and the vanadium-rich coating was a hydrated oxide with a composition of V2O5, VO2, and its hydrates such as V2O5.nH2O and VO（OH）2.

Electrochemical deposition of Mg(OH)_(2)/GO composite films for corrosion protection of magnesium alloys

Mg(OH)_(2)/graphene oxide(GO)composite film was electrochemical deposited on AZ91D magnesium alloys at constant potential.The characteristics of the Mg(OH)_(2)/GO composite film were investigated by scanning electron microscope(SEM),energy-dispersive X-ray spectrometry(EDS),X-ray diffractometer(XRD)and Raman spectroscopy.It was shown that the flaky GO randomly distributed in the composite film.Compared with the Mg(OH)_(2)film,the Mg(OH)_(2)/GO composite film exhibited more uniform and compact structure.Potentiodynamic polarization tests revealed that the Mg(OH)_(2)/GO composite film could significantly improve the corrosion resistance of Mg(OH)_(2)film with an obvious positive shift of corrosion potential by 0.19 V and a dramatic reduction of corrosion current density by more than one order of magnitude.

Corrosion resistance of cerium conversion film electrodeposited on Mg-Gd-Y-Zr magnesium alloy

The cerium conversion film was applied to improving the corrosion resistance of Mg-Gd-Y-Zr magnesium alloy. The film was electrodeposited on the surface of the Mg-RE alloy in cerium nitrate solution. The compositions and morphologies were analyzed by X-ray diffraction(XRD), scanning election microscopy (SEM). The corrosion behaviors of the film were investigated electrochemical impedance spectroscopy (EIS), potentiodynamic polarization tests and immersion tests. The results show that the optimum parameters for electrochemical deposition are as follows: pH 10.0, time 30 min, 50 mmol/L Na2CO3 and temperature 25 ℃ by the designed experiments according to the orthogonal table L(9, 34). The corrosion protection efficiency is dependent on the deposition parameters. The cerium conversion film shows better corrosion protection behavior than chromate conversion film on Mg-Gd-Y-Zr magnesium alloy.

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.

Multi-physics analysis of the galvanic corrosion of Mg-steel couple under the influence of time-dependent anisotropic deposition film

The anisotropic deposit film formed during the galvanic corrosion can impede the mass transfer of the involved species,thereby affecting the electro-chemical behavior and the evolution of galvanic corrosion.The limitations of experimental studies in the spatial-temporal scales restrict a deeper understanding of the corrosion mechanism,which can be complemented by numerical simulation.A multi-physics coupled model is proposed in this work to systematically investigate the temporal and spatial evolution of galvanic corrosion of the Mg-steel couple with the growing anisotropic deposition layer.By utilizing the multi-physics field coupled technique,various coupled physical-chemical processes underlying the corrosion behavior are built into the model,including chemical reactions,ionic mass transfer in the bulk solution and the deposition layer,interfacial reaction,deposition of corrosion products as well as the morphological transitions caused by metal dissolution and deposition.In particular,the anisotropic deposit film is considered to be a porous layer with a porosity varying in time and space as the corrosion evolves.The predicted corrosion morphology by this model is better than the previous models.The coupled relationship between the electrochemical behavior(e.g.,electrode reaction kinetics,current density,surface potential)and the physical processes(e.g.,ionic transport,geometric evolution of metal surface and film interface)is revealed.The results indicate that a porous deposition layer with a denser inner layer and a loose outer layer is generated,leading to more significant inhibition of mass transfer in the inner layer than the outer layer.The anisotropism of the deposition layer results in a non-uniform conductivity distribution and a discontinuous current density distribution in the electrolyte.The current density on the electrode surface is inhibited by the deposition layer and the variation in the cathode/anode area ratio during the corrosion process.The competition between the transport process and the electrochemical reaction determines the spatial-temporal evolution of the ion concentration.

PREPARATION AND CORROSION RESISTANCE OF NiP/TiO_2 COMPOSITE FILM ON CARBON STEEL IN SULFURIC ACID SOLUTION

A NiP/TiO2 composite film on carbon steel was prepared by electroless plating and sol-gel composite process. An artificial neural network was applied to optimize the prepared condition of the composite film. Corrosion behavior of the NiP/TiO2 composite film was investigated by polarization resistance measurement, anode polarization, ESEM （environmental scanning electron microscopy） and EIS （electrochemical impedance spectroscopy） measurements. Results showed that the NiP/ TiO2 composite film has a good corrosion resistance in 0.5mol/L H2SO4 solution. The element valence of the composite film was characterized by XPS （X-ray photoelectron spectroscopy） spectrum, and an anticorrosion mechanism of the composite film was discussed.

Effect of CO_2 on Atmospheric Corrosion of UNS G10190 Steel under Thin Electrolyte Film

The atmospheric corrosion of UNS G10190 steel under a thin electrolyte film in the atmosphere polluted by CO_2, has been studied in the lab using an atmospheric corrosion monitor (ACM) in combination with XRD and SEM observations of the surface of steel. The ACM study indicated that the corrosion rate of the steel increased with increasing carbon dioxide concentration. The XRD and SEM observations showed that no carbonate was found in the corrosion product on the steel surface. The corrosion product consisted of two layers, i. e., inner and outer layer. From the experimental results, it was concluded that CO_2 played an enhancing role in the atmospheric corrosion of UNS G10190 steel. The film of the corrosion product showed slight protection.

Corrosion behavior and characteristics of the product film of API X100 steel in acidic simulated soil solution

The short-term corrosion behavior of API X100 steel in an acidic simulated soil was investigated by electrochemical measurements and soaking experiments,followed by corrosion morphology observations and X-ray photoelectron spectroscopy analyses.The results show that X100 steel exhibits an obvious pitting susceptibility in an acidic soil environment.Pits nucleate after approximately 10 h of immersion.Along with the nucleation and growth of the pits,the charge-transfer resistance and open-circuit potential first increase sharply,then decrease slowly,and eventually reach a steady state.The maxima of the charge-transfer resistance and open-circuit potential are attained at approximately 10 h.The evolution of the electrochemical process is confirmed by the analysis of the product film.The product film exhibits a porous and loose structure and could not protect the substrate well.The product film is primarily composed of ferrous carbonate and ferrous hydroxide（Fe（OH）2）.The concentration of Fe（OH）2 in the product film increases from the inside to the outside layer.

CORROSION BEHAVIOR OF Cu-Nb AND Ni-Nb AMORPHOUS FILMS PREPARED BY ION BEAM ASSISTED DEPOSITION

The Cu25 Nb75 and Ni45Nb55 amorphous films with about 500nm thickness were prepared by ion beam assisted deposition (IBAD). Potentiodynamic polarization measurement was adopted to investigate the corrosion resistance of samples and the tests were carried out respectively in 1mol/L H2SO4 and NaOH aquatic solution. The corrosion performance of the amorphous films was compared with that of multilayered and pure Nb films. Experimental results indicated that the corrosion resistance of amorphous films was better than that of the corresponding multilayers and pure Nb films for both Ni-Nb system with negative heat of formation and Cu-Nb system with positive heat of formation.

Fabrication of Co-Ni-P film with excellent wear and corrosion resistance by electroplating with supercritical CO_2 emulsion

To avoid the defects caused by the hydrogen evolution and improve the corrosion and wear properties of the electroplated films in the traditional aqueous bath electrodeposition,a supercritical carbon dioxide(Sc-CO2)emulsion was proposed to electrodeposite ternary nanocrystalline Co-Ni-P alloy films.Microstructure,corrosive and tribological properties of the Co-Ni-P films were investigated and compared with the ones electroplated by conventional method.The results show that the Co-Ni-P films produced with Sc-CO2assisted electrodeposition exhibit a more compact microstructure.The preferred orientation plane of hcp(110)for the Co-Ni-P films produced in conventional aqueous bath is changed to be hcp(100)for the one prepared in emulsified Sc-CO2bath.The microhardness,corrosion resistance and tribological properties of the Co-Ni-P films are substantially improved with the assistance of Sc-CO2in the electrodeposition bath.

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.

Composition and corrosion resistance of palladium film on 316L stainless steel by brush plating

Palladium films with good adhesive strength were deposited on 316L stainless steel by brush plating. Scanning electronic microscopy, energy dispersive X-ray spectroscopy, X-ray photoelectron spectroscopy （XPS）, mass loss tests and electrochemical methods were used to study the properties of the films. The brush plated palladium film mainly consisted of palladium. XPS analysis indicated that palladium was present in the films as metal state. The palladium plated stainless steel samples showed excellent corrosion resistance in boiling 20% H2SO4 solution and boiling acetic/formic acids with 0.005 mol/L Br- ions added. The corrosion rates of the palladium plated 316L stainless steel samples were about two orders of magnitude lower than those of the original 316L stainless steel samples. This method provides a possibility to prepare protective palladium films on stainless steel facilities with large areas in industrial sites.