Effects of cerium salts on corrosion behaviors of Si–Zr hybrid sol–gel coatings

The present work examines the effects of cerium salts on corrosion behaviors of Si-Zr hybrid sol-gel coatings. The Si-Zr hybrid sol-gel coatings on a 2A l2 aluminum substrate were pre- pared through hydrolysis and condensation of glycidoxypropyl-trimethoxy-silane （GTMS） and zirconium（IV） n-propoxide （TPOZ）. Used as inhibitors for corrosion, three types of cerium salts （Co（NO3）3, CeCl3, and Ce（CH3COO）3） were doped into the sol-gel coatings. Fourier transform infrared （FTIR） and scanning electron microscopy （SEM） were employed to investigate the structures and morphologies of various coatings, and the corrosion resistances of the coatings were evaluated by electrochemical methods and neutral salt spray tests. Experimental results indicate that the addition of cerium salts can hinder the process of corrosion due to their self-healing abili- ties. Furthermore, the sol-gel coating doped with Ce（CH3COO）3 has the best corrosion resistance because of the promotions of hydrolysis and condensation provided by CH3COO-.

Cerium Salt Promoted Homocoupling Reaction of Dialkylanilines in Water

Highly regioselective homocoupling of N,N-dialkylanilines can be achieved in water with cerium reagents, in which various N,N,N′,N′-tetraalkylbenzidines are obtained from N,N-dialkylanilines either by direct oxidation by cerium（Ⅳ）reagents or by cerium（Ⅲ） reagents in the presence of hydroperoxide.

Post treatment of silane and cerium salt as chromate replacers on galvanized steel

A complex film on hot-dip galvanized steel sheet（HDG） was prepared by immersing the sheet in 0.1wt.% Ce（NO3）3 solution and 5vol.% silane solution in turn.The corrosion protection of the complex film was evaluated by potentiodynamic linear polarization（LPR）, electrochemical impendence spectra（EIS） and natural salt spray（NSS） tests and compared with that of single cerium film and silane film.The results showed that, the presence of these films on the zinc coating hindered corrosion reaction by reducing the rate of both anodic and cathodic reaction in the corrosion process, and the corrosion protection of the complex film was much better than that of single cerium film or silane film and closed to that of chromate film, because the polarization resistance Rp and electrochemical impendence were increased markedly.Microstructure and chemical composition of these pretreated films were also investigated by scanning electron microscopy（SEM） and AES.

Anodising of 2024-T3 aluminium alloy in electrolyte of sulphuric-boric-phosphoric mixed acid containing cerium salt as corrosion inhibitor

The effect of cerium salt as an inhibitor in anodising of the2024-T3aluminium alloy was studied.Scanning electronmicroscopy equipped with energy dispersive X-ray spectroscopy was used to study the surface composition of the alloy before andafter surface preparation.A mixed electrolyte of10%sulphuric acid,5%boric acid and2%phosphoric acid containing0.1mol/Lcerium sulphate salt was used as the anodising electrolyte.Sealing treatment was also done in boiling water and molten stearic acid.Electrochemical impedance spectroscopy and salt spray techniques were performed in order to investigate the corrosion behaviourand durability of the oxide films,respectively.It was concluded that the presence of cerium ions in anodising electrolyte resulted inthe increase in homogeneity,the rate of oxide film growth and also the thickness of the oxide layer,owing to the high oxidisingpower of cerium ion.

Combined influence of Ce(Ⅲ)and iodide ions for corrosion protection of AA 2024-T3 in acidic to neutral chloride-rich environments:Electrochemical and surface characterization studies

It has been reported that trivalent cerium salts are effective inhibitors for corrosion of AA2024-T3 in neutral to alkaline co rrosive enviro nments,but poor in acidic environments.In this study,work was done for extending corrosion resistance provided by Ce(NO_(3))_(3)to acidic pHs as low as 2.5 through the addition of iodide ions.To this end,potentiodynamic polarization was used to ascertain the optimum Ce(Ⅲ)concentration for the inhibition of AA2024-T3 corrosion in 3.5%NaCl solution.This optimum concentration is found to be in a range between 0.1 and 0.3 mmol/L Ce(Ⅲ).This optimum concentration also gives a maximum width of the passive region under the pitting potential(Epit).Based on this optimization,further work was performed as a function of pH without and in the presence of 0.01 mol/L KI at five pH values(2.5,4,5,7,and 8).Without iodide the best inhibition provided by the Ce(Ⅲ)cation is at pH=7 but active corrosion is observed at pH=2.5 with an estimated inhibitor efficiency(-37.6%).The addition of iodide ions(I^(-))reverses the poor corrosion resistance whereby the inhibitor efficiency becomes 47.7%.Moreover,at pH=4 the efficiency is also increased from 54.0%to 81.0%with iodide addition providing a significant improvement over Ce(Ⅲ)cations alone under acidic conditions.There is a synergistic effect between I-anion and Ce(Ⅲ)cation,which is determined to be 2.4 and 2.1 at pH=2.5and 4.0,respectively.At pH=5 and 7 there is virtually no change in inhibition but at pH=8 the inhibition falls away due to a considerable amount of cerium precipitating out of solution as cerium carbonate.The protective film formed on sites in the aluminium alloy surface at different pH values was examined by both scanning electron microscopy with energy dispersive X-ray analysis and X-ray photoelectron spectroscopy to determine the role of these ions as a function of pH in surface inhibition.It is proposed that at pH=2.5 protection is provided by a bilayer adsorption of iodide with"capping"cerium ions,but at pH=4 protection occurs through precipitate formation on active cathodes thereby shutting down the oxygen reduction reaction.