Investigation of Formation and Inhibition Mechanism of Cerium Conversion Films on Al 2024 Alloy

To study the mechanism of formation and inhibition of Ce conversion films on A1 2024-T3 alloy, scanning microreference electrode technique (SMRE) is used to probe the potential map on A1 2024-T3 in CeC13 solution, the localized corrosion of A1 alloy decreases with immersion time and disappears finally, which results from the competition of Cl^- aggression and Ce^3 inhibition on alloy surface. The results of X-ray photoelectron spectroscopy (XPS) indicate that the Ce conversion films consist of Al2O3, CeO2 and Ce2O3 (Ce(OH)3), and CeO2/Ce2O3 ratio decreases with the immersion time. When a critical pH for Ce(OH)3 formation was reached, Ce(OH)3 will precipitate on the micro cathodic area on alloy surface. Consequently, H2O2, the product of the catholic reaction will oxidize a part of Ce(OH)3 to CeO2, which appears a better corrosion resistance for Al alloys.     

Pitting corrosion behavior of cerium treated HSLA steel induced by sulfide inclusions in 3.5 wt% NaCl solution

Pitting corrosion behavior of Ce treated HSLA steels induced by sulfide inclusions in 3.5 wt% NaCl solution was investigated with potentiodynamic polarization and immersion corrosion test.The results show that Ce added steels exhibit better pitting corrosion resistance with lower corrosion current density and bigger pitting potential compared with steel without Ce,which is mainly attributed to optimized characteristics of spherical Ce-oxysulfide inclusions with less number density,smaller average size and lower pitting corrosion susceptibility.The spherical Ce₂O₂ S inclusions precipitated on the surface of CeAlO₃ inclusions in the Ce added steels induce pits with bigger opening mouth and shallow depth,reducing their tendency of extension to go deeper due to occlusion corrosion battery in the pitting holes.Furthermore,corrosion inhibitor Ce(OH)₃ generated by Ce₂O₂ S hydration can weaken electrochemical corrosion of the matrix micro-region around the pits.To avoid harmful bigger inclusions,Ce content in steels should be regulated within reasonable range,0.015 wt% Ce in present steels effectively modified inclusions to acquire the best pitting corrosion resistance of the steels.     

Corrosion protection of magnesium alloys anode by cerium-based anodization coating in magnesium-ait battery

CeN₃O₉·6H₂O(0.5,1.0,1.5,and 2.0 g/L) was added into an 8.0% NaCl electrolyte solution to investigate this electrolyte for use in a Mg-air battery.The effects of the amount of CeN₃O₉-6H₂O on the corrosion resistance of an AZ31 Mg alloy anode and battery performance were investigated using microstructure,electrochemical(dynamic potential polarization method and electrochemical impedance spectroscopy),and battery measurements.The re ...     

Cerium addition on pitting corrosion of (Cu50Zr50)100-2xCe2x (x=0, 1, 2 and 3) metallic glasses in seawater

The industrial application of metallic glass is a longstanding challenge for researchers in the field. Toward this objective, the electrochemical performance in sea water of Cu-Zr-(Ce) metallic glass with various Ce content was investigated. Cu-Zr-(Ce) metallic glass was fabricated by melt-spinning technique and characterized by X-ray diffraction. The corrosion resistance in seawater was then investigated by potentiodynamic polarization, immersion test, scanning electron microscopy, electron probe microanalysis, and energy dispersive spectrometer analysis. The results showed that Ce addition lowered the corrosion current density of Ce-containing Cu-Zr alloy system. The attack type changed from uniform corrosion of Cu50Zr50 metallic glasses to local one of the Ce-containing alloys. Appropriate content of Ce inhibited the selective dissolution of Cu in the pits and thus improved the corrosion resistance of the alloys.     

Influence of Cerium on Corrosion of AZ91 Magnesium Alloy

Effect of cerium addition on corrosion resistance of AZ91 magnesium alloy was investigated using the static weight loss and polarization curve method as well as metallographical observation. The results indicate that a small amount of cerium （0.2% - 0.8%） in AZ91 magnesium alloy can significantly reduce the corrosion rate, enhance the electrode voltage and lower corrosion current density in 3.5%NaCl aqueous solution, and AZ91-0.8% Ce alloy has better corrosion resistant performance. The reason for increasing corrosion resistance is attributed to the addition of Ce, refining the α-Mg grain, reducing the segregation of element Al, and improving the morphologies of β-Mg17 Al12 phases.     

Evaluation of Ce(Ⅲ) and Gd(Ⅲ) adsorption from aqueous solution using CTS-g-(AA-co-SS)/ISC hybrid hydrogel adsorbent

CTS-g-(AA-co-SS)/ISC hybrid hydrogel adsorbent with crosslinked network structure and superior adsorption performance for rare-earth metal ions was successfully synthesized in aqueous solution by a simple one-step free-radical grafting polymerization reaction among acrylic acid(AA), sodium p-styrenesulfonate(SS) and chitosan(CTS) using illite/smectite clay(ISC) as the inorganic additive. The structure of the as-prepared CTS-g-(AA-co-SS)/ISC hydrogel adsorbent was characterized, and the reaction parameters such as AA/SS molar ratio and ISC content were optimized, and the effects of pH values, initial concentration and contact time on the adsorption performance for Ce(Ⅲ) and Gd(Ⅲ) were systematically evaluated. It was found that the maximum adsorption capacities of the hydrogel adsorbent toward Ce(Ⅲ) and Gd(Ⅲ) reached 174.05 and 223.79 mg/g, respectively, and the adsorption quickly achieved equilibrium within 15–20 min. The adsorbed Ce(Ⅲ) and Gd(Ⅲ) could be easily desorbed for recovery, and the used adsorbent was able to be regenerated for reuse. After five adsorption-desorption cycles, the regenerated adsorbent could still retain the adsorption capacities that were close to the initial value. The adsorption process was well described by pseudo-second-order kinetic mode and the Langmuir isotherm model, and the chemical complexation between ions and –COO~–was mainly responsible for the high adsorption capacity. As a whole, the hybrid hydrogel adsorbent was potential to be used for the adsorption and recovery of Ce(Ⅲ) and Gd(Ⅲ) from water.     

Study of K~+ doping on structure and properties of γ-Ce_2S_3

In this study,K~+-doped γ-Ce_2 S_3 was successfully prepared via a gas-solid reaction method using CeO_2,K_2 CO_3,and CS_2 as raw materials.The effects of the suitable sulfide system and different molar ratios of K to Ce(n_(K/Ce)=0-0.30) on the phase composition,crystal structure,chromaticity and thermal stability ofγ-Ce_2 S_3 were systematically investigated.Pure γ-Ce_2 S_3 was obtained by calcining the doped samples at840℃ for 150 min.After calcination at the same temperature the undoped K+samples exhibit a pure α-phase.Samples with a K/Ce molar ratio(n_(K/Ce)) of 0.10-0.25 comprise only the γ-phase;and when n_(K/Ce) exceeds 0.25,a new heterogeneous phase,KCeS_2,emerges.For values of n_(K/Ce) in the range of0-0.25,the γ-Ce_2 S_3 lattice parameters gradually increases with increasing K~+ content.When n_(K/Ce)exceedes 0.25,the lattice parameters remains unchanged.As n_(K/Ce) increased,the synthesized color gradually changes from red to orange—red and finally,to yellow.The redness value a~* reaches the maximum(L~*=33.86,a~*=36.68,b~*=38.15) when n_(K/Ce)=0.10,The n_(K/Ce)=0.10 composition continues to exhibit the y-phase after heat treatment at 420℃ for 10 min in air.The K+doping fills the internal vacancies of γ-Ce_2 S_3 and formed a solid solution,which is beneficial for the stability of its lattice,thus improving the thermal stability of γ-Ce_2 S_3(from 350 to 420℃).     

Corrosion behavior of Ce-doped Ni-10Cu-11Fe-6Al (wt%) inert anode in molten CaCl2 salt

In this research the effect of cerium dopingon corrosion behavior of Ni-10 Cu-11 Fe-6 Al(wt%) alloy as a novel inert anode in titanium electrolytic production was investigated. The samples, including un-doped and Ce-doped nickel-based alloys, were prepared using vacuum induction melting(VIM) process and then exposed to the electrolysis in molten calcium chloride at 900C at à1.6 V versus graphite reference electrode for different immersion time. The surface and cross-section of the samples were characterized using scanning electron microscopy(SEM), and their electrochemical behavior was investigated by electrochemical impedance spectroscopy(EIS). The results show that the un-doped samples have greater number of voids and porosities as compared to that of the 0.0064 wt% Ce-doped samples(as the optimum content of cerium in the alloy). Thus, the nickel-based alloy becomes less sensitive to the pitting by addition of cerium. The corrosion penetration depth reaches about 244 mm after 16 h of electrolysis in the un-doped sample, while was approximately 103 mm for the 0.0064 wt% Ce-doped sample, which is an indication that the corrosion penetration depth decreases by adding small amounts of Ce.     

Effects of scandium chloride on osteogenic and adipogenic differentiation of mesenchymal stem cells

Mesenchymal stem cells(MSCs)are multi-potent cells that are able to differentiate and mature into various types of cells under a certain microenvironment for cell therapy and tissue regeneration.Scandium(Sc),an important rare earth element,recently has been intensively investigated in biomedical fields as well as industrial engineering,and chloride channels have been proven to be able to affect osteogenic differentiation.Thus,it is significant to investigate effects of ScCl₃on cell activities of MSCs.In this paper,rat bone MSCs(rBMSCs)were co-cultured with various concentrations of ScCl₃(1×10^-8,1×10^-6,and 1×10^-4mol/L)to evaluate their influence on cell proliferation as well as osteogenic and adipogenic differentiation in vitro.The results indicate that ScCl₃promotes the proliferation of rBMSCs initially,which is yet reduced upon ion accumulation.We used immunofluorescence staining,quantitative real time polymerase chain reactions,and assays measuring alkaline phosphatase activity,mineralized deposits,and intracytoplasmic lipids to reveal that rBMSCs treated with ScCl₃at concentrations of 1×10^-8-1×10^-6mol/L can enhance levels of osteogenic differentiation in a dosedependent manner and reduce adipogenic differentiation to a certain degree through Wnt/β-catenin signaling pathway.These results indicate that appropriate concentrations of ScCl₃can improve osteogenic differentiation in the lineage commitment of rBMSCs,and thus,promote bone remodeling.This study implies that ScCl₃ possesses great potentials in the treatment of bone diseases and would provide new strategy of designing composites by SiCl3 doping for biomedical applications in the future.     

Using EIS to evaluate anti-corrosion properties of the SiC_p/5A06 aluminium MMC treated by cerium conversion coatings

This paper evaluated the protection effect of the cerium conversion coatings on the SiCp/5A06 Al composite and the 5A06 Al alloy.Electrochemical impedance spectroscopy(EIS) was employed to examine the variation of the electrochemical variables of the samples treated and immersed in 3.5% NaCl solution at 35 °C for 1 h,which showed the enhancement of charge transfer resistance(Rt) and coating film resistance(Rc),i.e.,the corrosion resistance of the conversion coated samples was improved.The best protection effect was found for the samples treated for 60 min with 1000 μg/g CeCl3·7H2O/3.5% NaCl solution at 45 °C,followed with dried at 100 °C for 30 min.SEM/EDS examinations confirmed that the enhancement in corrosion resistance properties of these materials was due to the precipitation of cerium oxides/ hydroxides over the cathodic intermetallics and SiC particulates.The XPS results revealed that the conversion coatings were composed of CeO2,Ce2O3,Ce(OH)3,Ce(OH)4,and Al2O3.     

Superior corrosion resistance and corrosion mechanism of dual-main-phase (Ce15Nd85)30FebalB1M magnets in different solutions

The electrochemical corrosion behavior of both(Ce₁₅Nd₈₅)₃₀Fe_balB₁ M sintered magnets prepared with dual-main-phase method and N45-type magnets was studied in 3.5 wt% NaCl,1.1 wt% NaH₂ PO₄,and2.5 wt% NaOH solutions,respectively.The(Ce₁₅Nd₈₅)₃₀Fe_balB₁ M sintered magnets perform superior corrosion resistance than N45-type magnets in the tested solutions.In general,two ...     

A novel extractant bis(2-ethylhexyl) ((2-ethylhexylamino)methyl) phosphine oxide for cerium(IV) extraction and separation from sulfate medium

By introducing the amine group into phosphorus extractant, a novel aminophosphine compound bis(2-ethylhexyl) ((2-ethylhexylamino)methyl) phosphine oxide (DEHAPO, abbreviated as A) was synthesized for the extraction of cerium (IV) (Ce(IV)) from sulfate medium (H₂SO₄). The influence factors including extractant concentration, H₂SO₄ concentration and temperature on the Ce(IV) extraction were investigated and discussed. It is found that the extraction ability of Ce(IV), thorium (IV) (Th(IV)) and rare earths (REs(III)) (La, Gd, Yb) decreases in sulphate medium in the following order: Ce(IV) > Th(IV) > REs(III). The extraction process is an exothermic reaction and the thermodynamic parameters were calculated. The extracted complex of Ce(HSO₄)₂SO₄·A in loaded organic solution was identified by the slope methods and further proved by FT-IR spectral analysis. Stripping studies indicate that Ce(IV) can be effectively stripped from the organic phase. The results of separation factors (β) and saturation loading capacity demonstrate that DEHAPO could be used to selectively extract Ce(IV) from sulphate medium with high separation efficiency and good extraction ability.     

Electrochemical behavior of cerium ion in molten LiCI-KCI

The electrode process of cerium(Ⅲ) on the Mo electrode in eutectic LiCl-KCl melt was investigated by electrochemical transient techniques in the temperature range of 673-783 K,respectively.These results unanimously indicated that the reduction process of cerium(Ⅲ) to cerium metal was a single step exchanging three electrons which was controlled by diffusion of cerium(Ⅲ).Diffusion coefficients(D Ce(Ⅲ)) in eutectic LiCl-KCl melt were determined by cyclic voltammetry,chronopotentiometry and square wave voltammetry.An empirical diffusion coefficient function depending on temperature was proposed:lnD Ce(Ⅲ) =-2.129-5704/T.The formal potentials(Eθ’ Ce(Ⅲ)/Ce(0) versus Ag/AgCl reference electrode) at different temperatures were obtained from chronopotentiometry,which were-2.10 V(673 K) and-2.07 V(733 K),respectively.     

Solvent extraction of Ce(III) and Pr(III) with P507 using SiC foam as a static mixer

Extraction reactor is a major research area of interest within the field of rare earths extraction and separation. SiC foam offers excellent material characteristics as well as three-dimensional (3-D) reticulated structure; however, very little research has been carried out on its application in extraction reactor so far. In this work, a static mixer reactor based on SiC foam was designed and demonstrated to extract and separate Ce(III) and Pr(III) from nitric acid media by using 2-ethylhexyl phosphoric acid mono-2-ethylhexyl ester (P507) as extractant. The structure–performance relationship between SiC foam and extraction performance was studied by experiment combined with computational fluid dynamics (CFD) simulation. The experiment data are in good agreement with the simulation results. Contrast experiment by using a Kenics mixer was carried out, and SiC foam shows better extraction and mass transfer performance. Using the optimal structural SiC foam (pore size D = 2.3 mm, open porosity ε = 85%, foam length L = 80 mm), high extraction efficiency η (Pr(III): 94.6%, Ce(III): 88.5%) and separation factor β (2.27) between Ce(III) and Pr(III) is achieved at a high total throughput of 200 mL/min. Besides, overall volumetric mass transfer coefficient K_La of Pr(III) and Ce(III) are 0.519 and 0.378 s^?1 at the residence time τ of 3.6 s, respectively, which reach the high level of microchannel reactors and are better than conventional extractors and other static mixers. SiC foam is found to be applicable as a static mixer for efficient and high-throughput extraction and separation of rare earths.     

Synthesis of N,O-rich active site porous polymers and their efficient recovery of Gd(Ⅲ) from solution

Our previous study found that the adsorption performance of porous carbon for Gd(Ⅲ) could be significantly improved by increasing the N,and O functional groups on its surface.Unfortunately,the adsorption capacity of porous carbon is low due to the limited number of N,and O functional groups that can be loaded on its surface.Due to the advantage of customizable functional groups of porous organic polymers(POPs),the triazine-based Tb-MEL and hydroxyl-modified triazine-based Tp-MEL were synthesized...     

Adsorption and desorption properties of D151 resin for Ce(III)

The present research is aimed at the development of D151 resin as an adsorbent that it can be used in the adsorption of Ce(III) ions. The adsorption and desorption behaviors of Ce(III) on D151 resin have been investigated by chemistry analysis. The influence of operational conditions such as contact time, initial concentration of Ce(III), initial pH of solution and temperature on the adsorption of Ce(III) had also been examined. The results show that the optimal adsorption condition of D151 for Ce(III) was achieved at pH=6.50 in HAc-NaAc medium. The maximum uptake capacity of Ce(III) was 392 mg/g resin at 298 K. The adsorption of Ce(III) followed both the Langmuir isotherm and Freundlich isotherm, and the correlation coefficients had been evaluated. Even kinetics on the adsorption of Ce(III) had been studied. The adsorption rate constant k_{298 K} valued was 1.3×10^?5 s^?1. The calculation data of thermodynamic parameters which ΔS⁰ value of 91.34 and ΔH⁰ value of 7.07 kJ/mol indicate the endothermic nature of the adsorption process. While, a decrease of Gibb's free energy (ΔG⁰) with increasing temperature indicated the spontaneous nature of the adsorption process. Finally, Ce(III) could be eluted by using 0.5 mol/L HCl solution and the elution percentage was as high as 100%. Adsorption mechanism was also proposed for the adsorption of Ce(III) ions onto D151 resin using infrared spectroscopy technique.     

Effect of CuO species and oxygen vacancies over CuO/CeO2 catalysts on low-temperature oxidation of ethyl acetate

The catalytic oxidation of ethyl acetate(EA) was studied over CuO/CeO₂ catalysts which were prepared by ball milling with different precursors(copper oxide,cerium acetate,cerium dioxide,copper acetate and cerium hydroxide).The CuO/CeO₂ catalyst(O-A) prepared with copper oxide and cerium acetate as precursors shows very high catalytic activity that 100% EA conversion is achieved at low temperature of 220℃.It is found that specific surface area(112.8 m²/g),particle...     

Removal of chromium(III) by cation exchange resin, Indion 790 for tannery waste treatment

Extraction of chromium(III) from a model solution and from a tannery waste solution was studied by ion exchange using Indion 790 resin which is a macro-porous strongly acidic cation exchange resin of sulfonated polystyrene group. The resin was found to be selective for the sorption of chromium(III) in the pH range 0.5–3.5 from a model solution containing 500 ppm Cr(III). Beyond pH 3.5 extraction of chromium(III) drastically decreased from 92% to 76%. Sorption of chromium(III) on Indion 790 followed the Freundlich isotherm with a high Freundlich constant value (K_f = 8.57) confirming strong chemical interaction of the metal ion with the resin. Desorption of chromium(III) from the loaded resin increased with the increase in concentration of eluant (5–20% H₂SO₄). With 20% sulfuric acid solution 89% Cr(III) was eluted in two stages. The bench scale results were also validated in continuous mode in a fixed bed column and for the recovery of chromium(III) from a tannery solution.     

Microstructure and Mechanical Properties of Extruded Magnesium-Aluminum-Cerium Alloy Tubes

Current commercial magnesium extrusion alloys do not offer desirable combinations of strength, ductility, and extrusion speed for automotive structural applications. The effect of small additions of cerium (Ce) to pure magnesium (Mg) and Mg-3 pct Al alloy extruded tubes has been studied. The results suggest that 0.2 pct Ce addition can significantly improve the extrudability and mechanical properties of the Mg extrusions. The improvement in mechanical properties is due to grain refinement and dispersion strengthening provided by the Mg₁₂Ce particles and the beneficial texture obtained. Higher Ce contents further increase strength, but significantly reduce ductility and cause excessive surface oxidation during extrusion. The beneficial effect of 0.2 pct Ce on mechanical properties of pure Mg is not observed when it is added to Mg-3 pct Al alloy, due to the higher affinity of Ce to Al to form the Al₁₁Ce₃ phase in the Mg-Al-Ce ternary alloys. The Mg-0.2 pct Ce alloy is a promising base alloy for further development in automotive applications; however, Al should be avoided in Mg-Ce–based extrusion alloys.