Corrosion and antimicrobial property of TiO_(2)/Cu_(2)O and TiO_(2)/Cu_(2)O@CeO_(2)micro-arc oxidation coatings on Ti-6Al-4V alloys in natural seawater

Microarc oxidation is an effective surface treatment for improving certain properties of metals and their alloys.In this paper,TiO_(2)/Cu_(2)O and TiO_(2)/Cu_(2)O@CeO_(2)coatings were prepared on Ti-6Al-4V by microarc oxidation.Thecoatings exhibited good corrosion resistance and antimicrobial properties.X-ray diffraction(XRD),scanning electronmicroscopy(SEM),and 3D laser confocal were used to characterize the coatings.The properties of TiO_(2)/Cu_(2)O and TiO_(2)/Cu_(2)O@CeO_(2)coatings were analyzed,including microstructure,surface roughness,corrosion resistance,andantimicrobial properties.The electrochemical results showed that the coatings prepared by microarc oxidation hadenhanced corrosion resistance compared to the substrate.The antibacterial properties of TiO_(2)/Cu_(2)O and TiO_(2)/Cu_(2)O@CeO_(2)coating against Pseudomonas aeruginosa were evaluated by fluorescence microscopy and plate counting.The antibacterial rate of TiO_(2)/Cu_(2)O@CeO_(2)coating was up to 99.70%.In summary,the TiO_(2)/Cu_(2)O and TiO_(2)/Cu_(2)O@CeO_(2)coatings prepared by microarc oxidation have a potential application background in the field of marine corrosionprotection and biofouling.

Formation process of composite plasma electrolytic oxidation coating containing zirconium oxides on AM50 magnesium alloy

The formation processes of a composite ceramic coating on AM50 magnesium alloy prepared by plasma electrolytic oxidation （PEO） in a K 2 ZrF 6 electrolyte solution were studied by scanning electron microscope （SEM） and energy dispersive X-ray spectroscope （EDX）. Electrochemical impedance spectroscopy （EIS） tests were used to study the variation of the corrosion resistance of the coating during the PEO treatment. The results show that the coating formed on Mg alloy is mainly composed of MgO and MgF 2 when the applied voltage is lower than the sparking voltage, and zirconium oxides start to be deposited on Mg substrate after the potential exceeding the sparking voltage. The corrosion resistance of the coating increases with increasing the applied voltage.

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.

MICROSTRUCTURAL CHARACTERISTICSAND OXIDATION BEHAVIOR OFTi_(1-x)Al_xN PVD-COATINGS

Recent research on microstructural characteristics and oxidation behavior of Ti(1-x)AlxN thin film were surveyed. The Ti(1-x)AlxN coatings have three different phase regions, Bl structure for lower x value, wurtzite structure for higher x value and unidentified structure for medium x value. Based upon the selective oxidation mechanism the oxidation results of Ti(1-x)AlxN thin film with different Ti/Al ratio were predicated.

Removal of Uranium（Ⅵ） by Fixed Bed Ion-exchange Column Using Natural Zeolite Coated with Manganese Oxide

The adsorption of uranium(Ⅵ)on the manganese oxide coated zeolite(MOCZ)from aqueous solution was investigated in a fixed-bed column.The experiments were conducted to investigate the effects of bed height,flow rate,particle size,initial concentration of uranium(Ⅵ),initial pH,presence of salt and competitive ions.The U-uptake by MOCZ increased with initial uranium(Ⅵ)concentration and bed height,but decreased as the flow rate and particle size increased.In the presence of salt and competitive ions,the breakthrough time was shorter.The adsorption capacity reached a maximum at pH of 6.3.The Thomas model was applied to the experimental data to determine the characteristic parameters of the column for process design using linear regression.The breakthrough curves calculated from the model were in good agreement with the experimental data.The BDST model was used to study the influence of bed height on the adsorption of uranium(Ⅵ).Desorption of uranium(Ⅵ)in the MOCZ column was investigated.The column could be used for at least four adsorption-desorption cycles using 0.1mol.L-1 NaHCO3 solution as the elution.After desorption and regeneration with deionized water,MOCZ could be reused to adsorb uranium(Ⅵ)at a comparable capacity.Compared to raw zeolite,MOCZ showed better capacity for uranium(Ⅵ)removal.

Growth behaviour of low-energy plasma electrolytic oxidation coatings on a magnesium alloy

Plasma electrolytic oxidation(PEO),a promising surface treatment method to improve the corrosion and wear resistance of magnesium and its alloys,operates at high voltages,resulting in a relatively high energy cost.To make the PEO process more economically viable,its energy efficiency needs to be improved.This study investigates the growth behaviour and microstructural characteristics of low-energy PEO coatings on an AM50 magnesium alloy in a concentrated electrolyte containing sodium tetraborate.The surface morphology of the coatings was different from typical PEO coating morphologies and a large voltage oscillation was observed during treatment.Using different characterisation techniques,and based on a micro-discharge model,a correlation was made between the voltage-time behaviour,microdischarge characteristics and the composition and microstructure of the coated samples.The results suggest electrolyte chemistry can somewhat control discharge behaviour,which plays an important role in PEO coating growth.

Effects of additives on corrosion and wear resistance of micro-arc oxidation coatings on TiAl alloy

Ceramic coating was deposited on TiAl alloy substrate by micro-arc oxidation(MAO)in a silicate-aluminate electrolyte solution with additives including sodium citrate,graphite and sodium tungstate.The microstructures and compositions were analyzed by SEM,EDX and XRD.The corrosion and wear properties of the coatings were investigated by potentiodynamic polarization and ball-on-disc wear test,respectively.The results show that the MAO coatings consist of WO3,Ti2O3,graphite and Al2O3 besides Al2TiO5 and Al2SiO5.With additives in the electrolyte,the working voltage at the micro-arc discharge stage decreases,and the ceramic coating gets smoother and more compact.The corrosion current density of MAO coating is much lower than that of TiAl substrate.It can be reduced from 9.81×10-8A/cm 2to 3.02×10-10A/cm 2 .The MAO coatings composed of hard Al2O3,WO3 and Ti2O3 obviously improve the wear resistance of TiAl alloy.The wear rate is-3.27×10-7g/(N·m).

Effective modification of MgO with surface transition metal oxides for NF_3 decomposition

NF3 decomposition over transition metal oxides coated MgO reagents in the absence of water is investigated. The results show that NF3 can be decomposed completely over pure MgO but the time of NF3 steady full conversion kept as short as 80 min, while the reactivities of coated MgO reagents were remarkably enhanced by transition metal oxides, for example the time of NF3 complete conversion over 12%Fe/MgO extended to 380 min. It is suggested that not only an increase in surface area but also a significant enhancement in the fluorination of MgO substrate caused by the surface transition metal oxides result in an improved reactivity of coated MgO reagents for NF3 decomposition.

Oxide Coated Cathode Plasma Source of Linear Magnetized Plasma Device

Plasma source is the most important part of the laboratory plasma platform for fundamental plasma experimental research. Barium oxide coated cathode plasma source is well recognized as an effective technique due to its high electron emission current. An indirectly heated oxide coated cathode plasma source has been constructed on a linear magnetized plasma device. The electron emission current density can reach 2 A/cm2 to 6 A/cm2 in pulsed mode within pulse length 5-20 ms. A 10 cm diameter, 2 m long plasma column with density 10is m-3 to 1019 m3 and electron temperature Te --~ 3-7 eV is produced. The spatial uniformity of the emission ability is less than 4% and the discharge reproducibility is better than 97%. With a wide range of the plasma parameters, this kind of plasma source provides great flexibility for many basic plasma investigations. The detail of construction and initial characterization of oxide coated cathode are described in this paper.

Effect of Sputtered TiAlCr Coatings on Oxidation and Hot Corrosion Resistance of Ti-24Al-14Nb-3V

The effect of sputtered Ti-50Al-10Cr and Ti-50A1-20Cr coatings on both isothermal and cyclic oxidation resistance at 800-900℃ and hot corrosion resistance at 850℃ of Ti-24Al-14Nb-3V was investigated. Results indicated that Ti-24Al-14Nb-3V alloys exhibited poor oxidation resistance due to the formation of Al2O3+TiO2+AlNbO4 mixed scales in air at 800-900℃ and poor hot corrosion resistance due to the spoliation of scales formed in Na2SO4+K2SO4 melts at 850℃. Both Ti-50Al-10Cr and Ti-50Al-20Cr coatings remarkably improved the oxidation and hot corrosion resistance of Ti-24Al-14Nb-3V alloy.

Preparation of Hydroxyapatite-titanium Dioxide Coating on Ti6Al4V Substrates using Hydrothermal-electrochemical Method

Ti6Al4V substrates were anodized in a 0.5 mol/L H_2SO_4 solution at applied voltages of 90-140 V.A hydroxyapatite-titanium oxide（HA-TiO2）coating was then deposited on the anodized Ti6Al4 V substrates via a hydrothermal-electrochemicalmethod at a constant current.The obtained films and coatings were characterized by X-ray diffraction,scanning electron microscopy,energy-dispersive X-ray spectroscopy,and Fourier-transform infrared spectrometry.The microstructures of the porous films on the Ti6Al4 V substrates were studied to investigate the effect of the anodizing voltage on the phase and morphology of the HATiO_2 coating.The results indicated that both the phase composition and the morphology of the coatings were significantly influenced by changes in the anodizing voltage.HA-TiO_2 was directly precipitated onto the surface of the substrate when the applied voltage was between 110 and 140 V.The coatings had a gradient structure and the HA exhibited both needle-like and cotton-like structures.The amount of cotton-like HA structures decreased with an increase in voltage from 90 to 120 V,and then increased slightly when the voltage was higher than 120 V.The orientation index of the（002）plane of the coating was at a minimum when the Ti6Al4 V substrate was pretreated at 120 V.

Phase Evolution and Oxidation Resistance of YSZ/(Ni,Al) Composite Coatings in CH_4 Atmosphere

YSZ/（Ni, Al） composite coatings with different Ni：Al mole ratios were deposited on superalloy Inconel 600 by electrophoretic deposition（EPD） technique, followed by sintering in CH_4 atmosphere at 1 100 ℃for 2 h and isothermally oxidation at 1000 ℃ for 50 h. After sintering at 1100 ℃ for 2 h in CH_4 atmosphere, besides ZrC and t-ZrO_2 phases, the phase constitutes of Ni：Al mole ratios with 1：3, 1：2, and 1：1 were（Zr, Al）C, AlNi_3 and Ni phases, respectively. A remarkable difference in the oxidation behaviors of YSZ/（Ni, Al） composite coatings with different Ni：Al mole ratios was observed. For YSZ（Ni：Al=1：3） coated sample, oxidation at 1000 ℃ causes decomposition of the（Zr,Al）C solid solution to metallic Al, and then most of the Al is oxidized to Al_2O_3. For the YSZ（Ni：Al=1：2） coated sample, oxidation at 1000 ℃ mainly causes decomposition of the AlNi_3 phase. For YSZ（Ni：Al=1：1） coated sample, after oxidation at 1000 ℃, most of the Ni is oxidized to Ni O phase, and tolerated 50 h of oxidation and finally cracked and spalled from the specimen. YSZ（Ni：Al=1：3） and YSZ（Ni：Al=1：2） coated samples show superior oxidation resistance than that of YSZ coating. The different oxidation resistance mechanisms of YSZ/（Ni, Al） composite coatings sintered in CH_4 atmosphere were discussed.

Effect of Attapulgite Added in Plating Bath on the Properties of Ni/TiC Nano-composite Coatings

Pure copper plates were coated by Ni-TiC dipulse current plating method. The effects of adding different concentration（ranging from 0.5 g/L to 3.0 g/L） of attapulgite nano particles to the plating bath on the surface morphology, wear resistance, and oxidation resistance of Ni/TiC/Attapulgite nano-composite coatings were investigated. The experimental results show that the composite coating is flat and compact with adding 3.0 g/L in the bath, and the coating preferred orientation is changed from the planes（111） to（200）. The coefficient of the composite coatings decreases from 0.68 to 0.18 with increasing content of attapulgite in the bath, a mixed mode of adhesive-abrasive wear occurs for all coatings, and the wear mechanism shows a transition from adhesive-abrasive to predominantly abrasive wear mechanism when the concentration of attapulgite is beyond 1.5 g/L in electrolyte. The oxidation resistance of composite coatings is the best prepared when adding attapulgite particles at 0.5 g/L in the bath, the oxide mainly consists of a NiO phase by X-ray analysis.

Effect of rare earth Eu on anti-passivation of metal oxide anode coating

The anti passivation effect of metal oxide anode coating doped with rare earth element Eu was discussed. The morphology and the composition distribution of the metal oxide coating anode before and after electrolysis were studied by SEM and EDX analyses. The results show that the erosion of the electrolyte at the defects is the main cause for the failure of the coating. The erosion rate of the electrolyte is anisotropic. In area with high density of defects, the erosion rate is very fast and the failure of the coating is very quick. Moreover, the life time of the coating is prolonged by the doping of Eu. [

Formation and Oxidation Resistance of Silicide Coatings for Mo and Mo-Based Alloys

The forming process of silicide coatings on pure Mo and Mo-base alloys, obtained by the gas- phase deposition method. has been studied by examining the microstructure of coatings and the relationship between coating thickness and process parameters. It was shown that the growth of coatings was diffusion-controlled, the diffusion of silicon to be coated into Mo or Mo-base alloys was mainly responsible for the formation of silicide. The relationship between initial silicide thickness and oxidation resistance was also investigated, and the equation of service life of the coatings at high temperature in air is presented.

Micro-Crystalline Coatings of Co-Cr Dispersed with Y_2O_3 Deposited by Series Electro-Pulse Discharge

A new technique-series electro-pulse discharg e (SEPD)-was developed as a kind of surface coating process. In this technique, both positive and negative poles of a pulse power were used as the depositing electrodes with the substrate allo y as an induction electrode. Micro-crystalline Co-Cr and Co-Cr dispersed wit h Y 2O 3 coatings were deposited on Fe-18Cr-8Ni stainless steel surface by using Co30Cr alloy as the depositing electrodes. Oxidation at 950 ℃ in ambie nt air shows that these coatings greatly improve the oxidation resistance of the steel. The addition of dispersed Y 2O 3 nano-particles into the alloy coati ngs was found to further reduce the scaling rate and enhance the adhesion of oxi de scales.

Oxide coating mechanism during fluidized bed reduction: solid-state reaction characteristics between iron ore particles and MgO

Experiments on the solid-state reaction between iron ore particles and MgO were performed to investigate the coating mechanism of MgO on the iron ore particles＇ surface during fluidized bed reduction. MgO powders and iron ore particles were mixed and compressed into briquettes and, subsequently, roasted at different temperatures and for different time periods. A Mg-containing layer was observed on the outer edge of the iron ore particles when the roasting temperature was greater than 1173 K. The concentration of Fe in the Mg-containing layer was evenly distributed and was approximately 10wt%, regardless of the temperature change. Boundary layers of Mg and Fe were observed outside of the iron ore particles. The change in concentration of Fe in the boundary layers was simulated using a gas–solid diffusion model, and the diffusion coefficients of Fe and Mg in these layers at different temperatures were calculated. The diffusion activation energies of Fe and Mg in the boundary layers in these experiments were evaluated to be approximately 176 and 172 k J/mol, respectively.

Corrosion behavior of micro-arc oxidation coating on AZ91D magnesium alloy in NaCl solutions with different concentrations

Ceramic oxide coatings were prepared on AZ91D magnesium alloys in alkaline silicate solution using micro-arc oxidation（MAO） technique.The corrosion behavior of MAO coating on AZ91D magnesium alloys in NaCl solutions with different concentrations（0.1%,0.5%,1.0%,3.5% and 5.0% in mass fraction） was evaluated by electrochemical measurements and immersion tests.The results showed that the corrosion rate of the MAO coated AZ91D increased with increasing chloride ion concentration.The main form of corrosion failure was localized corrosion for the MAO coated AZ91D immersed in higher concentration NaCl solutions（1.0%,3.5% and 5.0%）,while it was general corrosion in dilute NaCl solutions（0.1% and 0.5%）.Two different stages of the failure process of the MAO coated AZ91D could be identified：1） occurrence of the metastable pits and 2） growth of the pits.Different equivalent circuits were also proposed based on the results of electrochemical impedance spectroscopy（EIS） for the MAO coated AZ91D immersed in different concentrations of NaCl solutions for 120 h.

Theoretical consideration on composite oxide scales and coatings

The present paper discussed some fundamental aspects on composite oxide scales and coatings for protection of alloys from high temperature oxidation, the related thermodynamic conditions, special mechanical characteristics and a sealing mechanism. It was proposed that the oxide scales and coatings with a composite structure should possess superior mechanical properties than that with a single phase oxide. It also showed that the A1203 scales or coatings doped with 3（203 and ZrO2 （or YSZ）-A1203 composite coatings possessed superior properties at high temperatures. In such composite oxide scales and coatings, the fracture resistance of the scales was increased by the toughening effect, the thermal stress was decreased owing to the increase of thermal-expansion coefficients, and A1203 phase could seal the alloy substrate well In addition, the kinetic equation of thermal growth oxide on alloy covered with composite oxide coatings was derived.

PREPARATION OF COMPLEX ZrO_2-Y_2O_3 SOL

Complex ZrO2-Y2O3 sol were prepared from precursors of inorganic salts and metal alkoxides. The processes for complex ZrO2-Y2O3 sol preparation and purification, the sol-gel transformation and the characterization of the sol from the two kinds of precursors were discussed and compared. It was found that the colloidal particles were amorphous in nature, and extremely fine (<10nm) in the both cases. ZrO2-Y2O3 coatings on GH220 superalloy samples MCrAlX (M=Fe, Co, Ni, X=Y, Ta,Hf…) pre-coated) were prepared using sols from the two different processes and tested at 1000 ℃ for 100 h in laboratory air. Results showed that only the coatings from the metal alkoxides derived sol offered excellent oxidation resistance.