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 per...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.展开更多
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...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.展开更多
A novel yttrium citrate-templated conversion method for morphology controlled synthesis of Y2O3 microspheres, microflowers and microsheets was reported for the first time. The precursors with controllable morphologies...A novel yttrium citrate-templated conversion method for morphology controlled synthesis of Y2O3 microspheres, microflowers and microsheets was reported for the first time. The precursors with controllable morphologies were synthesized with a homogenous precipitation method in aqueous solution without any surfactant. Y2O3 samples with well-preserved morphological architectures were obtained by a subse-quent thermal transformation strategy. The chemical formula of the precursor was identified and a two-stage growth mechanism was proposed. The effects of the aging time, reaction temperature, reactant concentration and molar ratio of yttrium nitrate to sodium citrate were discussed. The photoluminescence properties of the Y2O3：Eu3＋ microspheres, microflowers and microsheets prepared were also studied.展开更多
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 （...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.展开更多
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 o...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.展开更多
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. ...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.展开更多
The catalytic performance is highly related to the catalyst structure.Herein,a series of Ni nanoparticles supported on Y_(2)O_(3) with different morphologies were successfully synthesized via hydrothermal process scre...The catalytic performance is highly related to the catalyst structure.Herein,a series of Ni nanoparticles supported on Y_(2)O_(3) with different morphologies were successfully synthesized via hydrothermal process screening different pH environments.These Ni/Y_(2)O_(3)catalysts were applied to efficiently produce CO_(x)-free H2through ammonia decomposition.We identify a significant impact of Y_(2)O_(3)supports on nickel nanoclusters sizes and dispersion.The experimental results show that Ni/Y11 catalyst achieves 100% ammonia decomposition conversion under a gas hour space velocity(GHSV) of 12,000 ml·h^(-1)·gcat^(-1) and temperature of 650℃.Such a high level of activity over Ni/Y11 catalyst was attributed to a large specific surface area,appropriate alkalinity,and small Ni nanoparticles diameter with high dispersion.展开更多
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 affeci...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).展开更多
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, calcinatio...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.展开更多
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 o...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.展开更多
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 di...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.展开更多
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 condi...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.展开更多
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 investig...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.展开更多
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. Th...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 %.展开更多
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 ...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.展开更多
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 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.展开更多
Cyclic oxidation test is a fundamental method to assess lifetime of materials in high temperature environment.Cycle length or cyclic frequency is one important variable in cyclic oxidation testing.In present work,cycl...Cyclic oxidation test is a fundamental method to assess lifetime of materials in high temperature environment.Cycle length or cyclic frequency is one important variable in cyclic oxidation testing.In present work,cyclic oxidation tests were performed on cast K38 alloys with 0 wt.%,0.1 wt.%,and 0.5 wt.% yttrium additions at 1 273 K respectively.Two cyclic frequencies were used to investigate the influence of cycle length （1 h vs.20 h） on the high temperature oxidation behavior of superalloy.The results showed that the degradation of cast K38 alloy critically was dependent on the cyclic frequency.The yttrium addition was beneficial to reducing scale-growth rate,improving the scale adhesion and stress releasing,thereby increased the spallation resistance.It could be drawn that the effect of cyclic frequency was highly dependent on the scale adherence to the substrate.展开更多
Two experimental single crystal superalloys Y-free alloy and Y-containing alloy were cast in the directionally solidified furnace, while other alloying element contents were basically kept unchanged. The isothermal ox...Two experimental single crystal superalloys Y-free alloy and Y-containing alloy were cast in the directionally solidified furnace, while other alloying element contents were basically kept unchanged. The isothermal oxidation behavior of two single crystal superalloy was studied at 1100 ℃ in ambient atmosphere. Morphology of oxides was examined by scanning electron microscopy （SEM） and their compostion was analyzed by X-ray diffraction （XRD） and energy dispersive spectroscopy （EDS）. The effect of yt- trium on the high temperature oxidation resistance of the single crystal superalloy was investigated. The results showed that the oxi- dation resistance of Ni-base single crystal superalloy was substantially improved by adding a little amount of rare earth yttrium. Yt- trium could promote the oxide of A1 formation and decreased the proportion of NiO. Yttrium increased the coherence between the oxide scale and the alloy substrate to decrease the spallation of oxide scale. Yttrium reduced the oxide grain size and the thickness of oxide layer.展开更多
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...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.展开更多
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/80MP...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.展开更多
基金Project supported by SRF for ROCS, SEM (2003-14) and Science and Technology Department of Zhejiang Province (2003C11027)
文摘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.
基金National Natural Science Foundation of China(No.29231011)National Natural Science Foundation of Colombia(No.M018327)
文摘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.
基金Project supported by the National Natural Science Foundation of China (50990304)State "973" Project (2007CB936704)
文摘A novel yttrium citrate-templated conversion method for morphology controlled synthesis of Y2O3 microspheres, microflowers and microsheets was reported for the first time. The precursors with controllable morphologies were synthesized with a homogenous precipitation method in aqueous solution without any surfactant. Y2O3 samples with well-preserved morphological architectures were obtained by a subse-quent thermal transformation strategy. The chemical formula of the precursor was identified and a two-stage growth mechanism was proposed. The effects of the aging time, reaction temperature, reactant concentration and molar ratio of yttrium nitrate to sodium citrate were discussed. The photoluminescence properties of the Y2O3：Eu3＋ microspheres, microflowers and microsheets prepared were also studied.
基金supported by the Natural Science Foundation of Henan Province (200510476009)
文摘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.
文摘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.
文摘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.
基金financially supported by the National Natural Science Foundation of China (Nos.21868016, 21763018,22005296 and 21875096)the Key Laboratory for Environment and Energy Catalysis of Jiangxi Province (No. 20181BCD40004)+1 种基金the Natural Science Foundation of Jiangxi Province (No.20181BAB203016)the Graduate Students Innovation Special Foundation of Jiangxi Province (No.YC2021-B014)。
文摘The catalytic performance is highly related to the catalyst structure.Herein,a series of Ni nanoparticles supported on Y_(2)O_(3) with different morphologies were successfully synthesized via hydrothermal process screening different pH environments.These Ni/Y_(2)O_(3)catalysts were applied to efficiently produce CO_(x)-free H2through ammonia decomposition.We identify a significant impact of Y_(2)O_(3)supports on nickel nanoclusters sizes and dispersion.The experimental results show that Ni/Y11 catalyst achieves 100% ammonia decomposition conversion under a gas hour space velocity(GHSV) of 12,000 ml·h^(-1)·gcat^(-1) and temperature of 650℃.Such a high level of activity over Ni/Y11 catalyst was attributed to a large specific surface area,appropriate alkalinity,and small Ni nanoparticles diameter with high dispersion.
文摘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).
文摘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.
基金Funded by the National Natural Science Foundation of China (No. 51003082)the Key Project of Science and Technology Research of Ministry of Education (No. 208089)+2 种基金the Educational Commission of Hubei Province (No.Q20101606)the Young Outstanding Talent Foundation of Hubei Province (No.2008CDB261)the Natural Science Foundation of Hubei Province (No. 2007ABA075)
文摘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.
基金supported by the National Natural Science Foundation of China(No.51075285) the Provincial Natural Science Foundation of Liaoning in China(No.20102222)
文摘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.
基金Supported by the National Natural Science Foundation of China(Nos.20704036, Key Program 20434020)the State Basic Research Projects of China(No.2005CB623802)
文摘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.
基金supported by the National Natural Science Foundation of China (Grant No. 60578041)the Shanghai Leading Academic Disciplines (Grant No. S30107)
文摘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.
文摘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 %.
基金Project supported by key project of science and technology research of guangdong province(2002A1070108)
文摘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.
基金The Natural Science Foundation of Higher EducationInstitutions of Jiangsu Province (No.04KJB510073).
文摘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.
基金Project supported by the Science and Technology Funds from Liaoning Education Department (2008564)the National Natural Science Foundation of China (50771100)
文摘Cyclic oxidation test is a fundamental method to assess lifetime of materials in high temperature environment.Cycle length or cyclic frequency is one important variable in cyclic oxidation testing.In present work,cyclic oxidation tests were performed on cast K38 alloys with 0 wt.%,0.1 wt.%,and 0.5 wt.% yttrium additions at 1 273 K respectively.Two cyclic frequencies were used to investigate the influence of cycle length （1 h vs.20 h） on the high temperature oxidation behavior of superalloy.The results showed that the degradation of cast K38 alloy critically was dependent on the cyclic frequency.The yttrium addition was beneficial to reducing scale-growth rate,improving the scale adhesion and stress releasing,thereby increased the spallation resistance.It could be drawn that the effect of cyclic frequency was highly dependent on the scale adherence to the substrate.
文摘Two experimental single crystal superalloys Y-free alloy and Y-containing alloy were cast in the directionally solidified furnace, while other alloying element contents were basically kept unchanged. The isothermal oxidation behavior of two single crystal superalloy was studied at 1100 ℃ in ambient atmosphere. Morphology of oxides was examined by scanning electron microscopy （SEM） and their compostion was analyzed by X-ray diffraction （XRD） and energy dispersive spectroscopy （EDS）. The effect of yt- trium on the high temperature oxidation resistance of the single crystal superalloy was investigated. The results showed that the oxi- dation resistance of Ni-base single crystal superalloy was substantially improved by adding a little amount of rare earth yttrium. Yt- trium could promote the oxide of A1 formation and decreased the proportion of NiO. Yttrium increased the coherence between the oxide scale and the alloy substrate to decrease the spallation of oxide scale. Yttrium reduced the oxide grain size and the thickness of oxide layer.
文摘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.
文摘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.
