Synthesis of Yttrium Oxide Nanocrystal via Solvothermal Process

Y2O3 nanomaterials have been widely used in transparent ceramics and luminescent devices. Recently there are many studies focusing on controlling the size and morphology of Y2O3 in order to obtain better materials performance. In present study, yttrium oxyhydroxide precursor was synthesized via a facile solvothermal process through the dissolution-re-crystallization mechanism of Y2O3 raw powders in the ethylenediamine solvent, then nanosized yttrium oxide crystal was prepared from the precursor through post heat treatment process. The effects of solvothermal treatment temperature, holding time, solvent kinds and post heat treatment parameters on crystalline structure, grain shape and size of nanocrystal were investigated by XRD, TEM and TGA-DTA measurements. TEM images reveal that the morphology of product after post heat treatment at 460℃for 12 h is rice-like nanocrystal. XRD shows that this product is pure cubic Y2O3 cphase. Present study reveals that high purity Y2O3 with rice-like morphology can be easily prepared with average size around 30 nm under suitable post heat treatment parameters. In addition, the effects of solvents such as water and ethanol etc. on the crystal structure and morphology were also investigated. It is suggested that dissolution-recrystallization process may be the main mechanism for the formation of nano-sized YOOH precursors under solvothermal reaction condition, and the ethylenediamine solvent is likely to play an important role in controlling the transformation process of yttria precursors to the Y2O3 nanocrystal.

Influence of Yttrium Ion-Implantation on the Growth Kinetics and Micro-Structure of NiO Oxide Film

Isothermal and cyclic oxidation behaviours of pure and yttrium-implanted nickel were studied at 1000℃ in air. Scanning electronic microscopy （SEM） and transmission electronic microscopy （TEM） were used to examine the micro-morphology and structure of oxide scales formed on the nickel substrate. It was found that Y-implantation significantly improved the anti- oxidation ability of nickel in both isothermal and cyclic oxidizing experiments. Laser Raman microscopy was also used to study the stress status of oxide scales formed on nickel with and without yttrium. The main reason for the improvement in anti-oxidation of nickel was that Y- implantation greatly reduced the growing speed and grain size of NiO. This fine-grained NiO oxide film might have better high temperature plasticity and could relieve parts of compressive stress by means of creeping, and maintained a ridge character and a relatively low internal stress level. Hence yttrium ion-implantation remarkably enhanced the adhesion of protective NiO oxide scale formed on the nickel substrate.

Study on phosphating treatment of aluminum alloy:role of yttrium oxide

Zinc phosphate coatings formed on 6061-Al alloy, after dipping in phosphating solutions containing different amounts of Y2O3（yttrium oxide）, were studied by scanning electron microscopy （SEM）, X-ray diffraction （XRD） and electrochemical measurements. Significant variations in the morphology and corrosion resistance afforded by zinc phosphate coating were especially observed as Y2O3 in phosphating solution varied from 0 to 40 mg/L. The addition of Y2O3 changed the initial potential of the interface between aluminum alloy substrate and phosphating solution and increased the number of nucleation sites. The phosphate coating thereby was less porous structure and covered the surface of aluminum alloy completely within short phosphating time. Phosphate coating was mainly composed of Zn3（PO4）2·4H2O （hopeite） and AlPO4（aluminum phosphate）. Y2O3, as an additive of phosphatization, accelerated precipitation and refined the gain size of phosphate coating. The corrosion resistance of zinc phosphate coating in 3% NaCl solution was improved as shown by polarization measurement. In the present research, the optimal amount of Y2O3 was 10-20 mg/L, and the optimal phosphating time was 600 s.

Preparation and Characterization of Porous Yttrium Oxide Powders with High Specific Surface Area

The porous cubic yttrium oxides with high specific surface area were prepared yttrium nitrate and its complex formed with methyl salicylate. The specific surface area by the explosive decomposition of and properties of powders synthesized at various temperatures were characterized using BET, X-ray diffraction （XRD）, infrared spectra （IR）, and scanning electron microscopy （SEM）. The results indicate that the highest specific surface area is found to be 65.37 m^2·g^-1 at the calcination temperature of 600 ℃, and then decreases to 20.33 m2· g^- 1 with the calcination temperature rising from 600 to 900 ℃. The powders show strong surface activity for adsorping water and carbon dioxide in air, which also decreases with the rising calcination temperature. The drop both on the surface area and surface activity of samples at higher temperatures may be due to pore-narrowing（sintering） effects.

Influences of Yttrium on Adhesion of Oxide Scale of Fe-Cr-Al Alloy

The 1100 degreesC isothermal oxidation behavior of Fe-23Cr-5Al alloy modified by yttrium addition was studied by means of thermogravimetric analysis, scanning electron microscopy and energy dispersive X-ray analysis. Yttrium was added to this alloy in the forms of metallic addition, yttrium oxide and ion implant. Cracking and spalling occurred on the convoluted scale formed on Y-free alloy and exposed the substrate. A flat dense scale without spallation was formed on the yttrium alloying addition or yttrium oxide dispersion alloy. The scale adhesion was also improved by 1x10(17)Y(+)/cm(2)-implantation. The results indicate the convoluted morphology of the scale on Fe-23Cr-5Al-0.21Ti alloy is related to the growth mechanism of the alumina scale, and the spallation of the scale is related to sulfur segregation at the scale/alloy interface. The main reason that the adhesion of alumina scale is improved by yttrium addition lies in the following. Yttrium is liable to form a stable yttrium sulfide with sulfur in the alloy and prevent sulfur interface from segregation. Another reason is that the growth mechanism of alumina scale is changed by yttrium addition.

Determination of Trace Impurities of Rare Earth Elements in High Purity Yttrium Oxide by ICPMS

Determination of trace rare earth elements(REEs)in 99. 999% purity yttrium oxide using the inductively coupled plasma mass spectrometric technique (ICPMS) has been developed. Instrumental parameters and factors affecitng analytical results have been studied and then optimized.Samples are analyzed directly following an acid digestion without separation or preconcentration and with limit of detection of 0. 003～0. 02 ng/ml, precision of ±5. 4%(cofficient of variation)and recovery of 90～115%. Correction for isobaric interferences from oxide ions and hydroxide ions is made mathematically. Special internal standard procedures are used to compensate drift in metal:metal oxide ratios and sensitivity. The analytical results of several samples are accurate as compared with inductively coupled plasma atomic emission spectrometry (ICPAES) and spark source mass spectrometry (SSMS).

Synthesis and Characterization of Large Surface Area Yttrium Oxide by Precipitation Method

The method for preparing yttrium oxide with large specific surface area was introduced. By means of BET, SEM, TG and DTA analysis, the effects of precipitant, stirring velocity, non-RE impurity in solution, calcination temperature, on the surface area were studied respectively. The Y_2O_3 sample with specific surface area of more than 60 m^2·g^(-1) and L.O.I less than 1% was prepared in the suitable precipitation condition and calcinations temperature when the ammonia used as precipitant. The SEM shows that the Y_2O_3 prepared with large surface area is the aggregation of about 50 nm particles.

Thermal, Mechanical and Electrical Properties of the PEO-based Solid Polymer Electrolytes Filled by Yttrium Oxide Nanoparticles

The novel composite lithium solid polymer electrolytes （SPEs） composed of polyethylene oxide （PEO） matrix and yttrium oxide （Y2O3） nanofillers were prepared by a solution casting method. The crystal morphology of the SPEs was characterized by polarized optical microscope （POM） and wide-angle X-ray diffraction （WAXD）. The induced nucleation and steric hindrance effects of Y2O3 nanofillers result in the increased amount as well as decreased size of PEO spherulites which are closely related to the crystallinity of the SPEs. As the Y2O3 contents increase from 0 wt% to 15 wt%, the crystallinity of the SPEs decreases proportionally. The thermal, mechanical and electrical properties of the SPEs were investigated by thermal gravimetric analysis （TGA）, dynamic mechanical analysis （DMA） and AC impedance method, respectively. The physical properties including thermal, mechanical and electrical performances, depending remarkably on the polymer-filler interactions between PEO and Y2O3 nanoparticles, are improved by different degrees with the increase of Y2O3 contents. The （PEO）21LiI/10 wt%Y2O3 composite SPE exhibits the optimal room-temperature ionic conductivity of 5.95×10-5 Scm-1, which satisfies the requirements of the conventional electrochromic devices.

Interfacial reaction between zirconium alloy and graphite mold/yttrium oxide ceramic mold

Zirconium alloys are active in the molten state and tend to react with the mold during casting. The casting technology of zirconium is not yet well established; especially in selecting the mold materials, which are difficult to determine. In the present work, the interfacial reactions between zirconium casting and casting mold were studied. The zirconium alloy was melted in a vacuum arc skull furnace and then cast into the graphite mold and ceramic mold, respectively. The zirconium casting samples were characterized using SEM, EDS and XRD with an emphasis on the chemical diffusion of elements. A reaction layer was observed at the casting surface. Chemical analysis shows that chemical elements C, O and Y from the mold are diffused into the molten zirconium, and new phases, such as ZrC, Zr30, YO1.335 and Y6ZrO11, are formed at the surface. In addition, an end product of zirconium valve cast in a yttria mold has a compact structure and good surface quality.

Ring-opening Copolymerization of Adipic Anhydride and Propylene Oxide Catalyzed by Yttrium Triflates

The ring-opening copolymerization of adipic anhydride with propylene oxide was carried out with yttrium triflates as a catalyst. Poly（propylene adipate） could be synthesized by controlling the copolymerization conditions. The copolymerization procedure was tracked by ^1H NMR analyses.

Spectral properties of Ce^(3+) doped yttrium lanthanum oxide transparent ceramics

Ce3＋-doped yttrium lanthanum oxide （Y0.9La0.1）2O3 transparent ceramics is fabricated with nanopowders and sintered in H2 atmosphere. The spectral properties of Ce：（Y0.9La0.1）2O3 transparent ceramics are investigated. There appear two characteristic absorption peaks of Ce3＋ ions at 230~nm and 400~nm, separately. It is found that Ce3＋ ions can efficiently produce emission at 384~nm from （Y0.9La0.1）2O3 transparent ceramic host, while the emission is completely quenched in Re2O3 （Re=Y, Lu, La） host materials.

Synthesis, characterization of a multi-component metal oxide (Al_0.88Fe_0.67Zn_0.28O₃) and elimination of As (III) from aqueous solution.

The multi-component oxide (Al0.88Fe0.67Zn0.28O3)) surface (abbreviated as MCOS) was prepared to optimize the effectiveness of the elimination of As (III) from aqueous solution. The oxide surface was synthe-sized by co-precipitation method using corresponding metal carbonates. It was characterized by XRD, TGA and DSC. The surface morphology of MCOS was observed in SEM and the elemental analysis was accomplished by EDX. The composition of Al2O3, Fe2O3 & ZnO was 23.6, 39.9 and 20.6 wt% respectively in XRF analysis. The specific surface area was found 389.85 m2 g-1. Batch experiments were performed to remove As (III) from aqueous solution considering various parameters such as effect of pH, contact time, initial arsenic concentration, temperature and sor-bent dosage. The maximum sorption capacity of the surface was almost steady from pH 4 to pH 9. Kinetic study shows that As (III) sorption is following second order rate equation with the rate constant of 80×10-2 g mg-1 min-1 at room temperature and this rate was increased with increasing temperature which indicates the sorption was endothermic process. The free energy change, ΔGo was negative which proves that the sorption was spontaneous and thermodynamically favorable. Sorption isotherm was interpreted by Langmuir equation and the maximum sorption capacity of oxide monolayer was 13×10-2 mg g-1.

Preparation of Yttrium－Barium－Copper Trinary Master Alloys by Electrolysis from Molten Fluoride－oxide

The electrochemical behaviour of Y￣(3+) and Ba￣(2+) on platinum and copper electrode in molten YF_3(70 wt% )-NaF (20 wt%)-CaF_2(10 wt%) has been studied by means of cyclic voltammetry. discharge curve and so on. The Y-Ba-Cu alloy is obtained by fused salt electrolysis with molten YF_3-NaF-CaF_2 as electrolyte and Y_2O_3 and BaO as raw materials. Graphite cell acted as an anode and copper rod as consumable cathode. The molten bath temperature was 1193 K. Cathode current density was 20 A/cm￣2. The contents of yttrium, barium and copper in alloy were about 20wt%, 9 wt% and 71 wt% respectively. Yttrium recovery efficiency was 90 wt%. The current efficiency was 70%～80 %.

Preparation of nanometer yttrium oxide

The nanometer yttrium oxides were obtained through precipitation in aqueous solution by reaction with ammonium bicarbonate. The reaction between yttrium chloride and ammonium bicarbonate, the effect of surfactants on particle size and the methods of controlling agglomeration were studied. Compared to other methods, the method of controlling the agglomeration by adding surfactant is one of the best methods for controlling the agglomeration of nanometer particles in wet-chemical process. Increasing surfactants in process of precipitation deduced particle size, obtained narrow size distribution of primary particles. As for the concentration range studied, excess surfactants increased the particle size on the contrary. Characteristics of the thermal decomposition of yttrium carbonate were studied. It indicated that the approximate chemical composition of the precipitate was Y（OH）Clx（CO3） （1-x/2） ·3H2O,the cubic Y2O3 was obtained above 600℃, the specific surface and the remain chloride of nanometer Y2O3 was decreased with calcinating temperature rising. The spherical nanometer yttrium oxide was gained with primary particles<50 nm,agglomerate distribution D 50 <150 nm, BET>35 m2/g,agglomerate constant （D 50 /D BET ）<6.

Oxide/substrate interfacial defects in high temperature oxidation of Co-40Cr by acoustic emission method

The isothermal oxidation kinetics of a Co-40Cr alloy and its yttrium ion-implanted samples were studied at 1000℃ in air by thermal-gravity analysis （TGA）. Scanning electronic microscopy （SEM） was used to examine the Cr203 oxide film＇s morphology after oxidation. An acoustic emission （AE） method was used in situ to monitor the cracking and spalling of oxide films formed on samples during oxidation and subsequent aircooling stages. A theoretical model was proposed relating to the film fracture process and was used to analyze the acoustic emission spectrum on time domain and the AE-event number domain. It was found that yttrium implantation remarkably reduced the isothermal oxidation rate of Co-40Cr and improved the anti-cracking and anti-spalling properties of Cr2O3 oxide film. The reasons for the improvement were mainly that the implanted yttrium reduced the grain size of Cr2O3 oxide, increased the high temperature plasticity of oxide film, and remarkably reduced the number and size of Cr203/Co-40Cr interfacial defects.

Effect of Yttrium on High Temperature Oxidation Resistance ofa Directionally Solidified Superalloy

The effect of rare earth element yttrium on the high temperature oxidation resistance of a directionally solidified Ni-base superalloy was studied with scanning electron microscopy(SEM), energy dispersive spectrum(EDS)and X-ray diffraction(XRD)techniques. The results show that the oxidation resistance of the alloy is substantially improved by adding proper amount of yttrium.

IMPROVEMENT OF OXIDATION RESISTANCE AND MECHANICAL PROPERTIES BY THE ADDITION OF YTTRIUM AND SILICON IN A Ni_3Al BASE ALLOY IC6

The oridation resistance at 1100°C of a dirationally solidified Ni3Al base alloy IC6is substantially improved by the addition of yttriurn or yttrium and silicon. The stress rupture property under 1100°C/80MPa is increased by adding proper amounts of yttrium, howevef it decreases bg adding 0.3wt% silicon and 0. 1wt% yttrium at the same time, which may be attributed to the formation of a needle like phase rich in nickel and molybdenum.

Gasoline Sensor Based on Rare Earth-Doped Indium Oxide with Low Power Consumption

Nanocrystalline indium oxide powders were prepared by microemulsion and then Y2O3 and Nd2O3 doped In2O3 were synthesized separately by impregnation and chemical co-deposition. The structure and morphology were characterized by XRD and TEM, respectively. Gas sensing properties were tested at static state. The results show that homogeneous indium oxide nanopowder with main grain size of 20 nm can be obtained from microemulsion after sintered at 600 ℃ for 1 h. Pure indium oxide gas sensor has higher sensitivity to gasoline than that to ethanol, HCHO, C6H6, NH3, C4H10, but the selectivity is not as well as sensitivity.

Effects of Yttrium Ion on Formation Mechanism of ZrO_2-Y_2O_3 Ceramic Coatings Formed by Plasma Electrolytic Oxidation on Al-12Si Alloy

ZrO2-Y2O3 ceramic coating was produced by plasma electrolytic oxidation （PEO） on ZAlSil2Cu3Ni2 alloy. The microstructure and phase composition of the coating were investigated by SEM and XRD.： The results show that adding an appropriate amount of yttrium ion can improve the growing rate of ceramic coating at different oxidation stages and decrease arc voltage. The thickness of ZrO2-Y2O3 coating is 16 μn thicker than that of ZrO2 coating and the maximum oxidation rate improves by 0.6 μm/min. In addition, the arc voltage decreases from 227 to 172 V. It can be seen that the rate of oxidation firstly increases to some extent and then decreases with the content of yttrium ion increasing. The growth rate reaches the maximum while the content of yttrium ion is 0.05 g-L-1The maximum thickness is 90 μm.Compared to ZrO2 coating, the micropores of ZrO2-Y2O3 coating are less and the ceramic layer is repeatedly deposited by ZrO2 and Y2O3 ceramic particles. Meanwhile, the binding force between coating and substrate is better and the coating is uniform and compact. The ceramic layer is mainly composed of c-Y0.15Zr0.85O1.93□0.07, m-ZrO2, α-Al2O3, ,γ-Al2O3 and Y2O3. It is indicated that ZrO2 has beert fully stabilized by yttrium ion through the formation of solid solution.

Interfacial Behavior of Sulfur and Yttrium in Yttrium Modified Ni _3Al Based Alloy IC6 during High Temperature Oxidation Process

The interfacial behavior of sulfur and yttrium in the yttrium modified Ni 3Al based alloy IC6 during oxidation at 1100 ℃ was analyzed by X ray line scan of electron probe microstructural analysis(EPMA). The results show that the migration and segregation of sulfur to the interface between oxide scale and the substrate at high temperature is retarded owing to the presence of yttrium. This is attributed to the desulfurization by yttrium in the melt and the trapping of sulfur by yttrium rich phases during oxidation, which leads to improving the coherence between oxide scale and substrate. Another reason of increasing the high temperature oxidation resistance of alloy IC6 by the addition of yttrium is that yttrium migrates to the grain boundaries of oxides during oxidation and hence improve their strength. This results in the transformation of the oxide scale spallation cracks from intergranular cracks for alloy without yttrium to transgranular ones for yttrium modified alloy.