This work focused on the zinc powder coated with Y(OH)3 microparticles by means of ultrasonic immersion for performance improvement of zinc electrodes in alkaline battery systems.Scanning electron microscopy and other...This work focused on the zinc powder coated with Y(OH)3 microparticles by means of ultrasonic immersion for performance improvement of zinc electrodes in alkaline battery systems.Scanning electron microscopy and other characterization techniques were applied to examine the influence of the ultrasonic power on the sonochemical growth of Y(OH)3 microparticles in direct contact with zinc powder.Electrochemical properties of zinc electrodes containing Y(OH)3 microparticles were discussed through the measurement...展开更多
The phase and morphology transformation during the hydrothermal treating process of Y2O3 was evaluated with X-ray difference (XRD), scanning electron microscopy (SEM), transmission electron microscopy (TEM), particle ...The phase and morphology transformation during the hydrothermal treating process of Y2O3 was evaluated with X-ray difference (XRD), scanning electron microscopy (SEM), transmission electron microscopy (TEM), particle size and specific surface area determination. The results showed that the cubic Y2O3 did not transfer into hexagonal Y(OH)3 in pure water. Therefore, pure hexagonal Y(OH)3 with nanotube and microrod morphologies were obtained by hydrothermal treating Y2O3 at 150 oC for 12 h in 15 ml of 2 mol/L NaOH solution with and without PVA or PEG. It was suggested that the characteristic preferential growth of Y(OH)3 was attributed to the structure anisotropy of hexahedron Y(OH)3. The addition of PVA or PEG could promote the forming process of nanotubes by selective adsorption on different crystal planes, which altered the growth rate along different directions and resulted in the diffusion limit of constructing ions in the center top of rods. Finally, Y(OH)3:Eu and Y2O3:Eu nanotubes were also synthesized by using this method, and their photoluminescence properties were evaluated.展开更多
The new electrorheologicai （ER） material, a particle material composed of Y4O（OH）9（NO3） and NH4NO3, was obtained. They display better ER performance. The shear stress of the suspension of Y4O （OH）9 （NO3） （ ...The new electrorheologicai （ER） material, a particle material composed of Y4O（OH）9（NO3） and NH4NO3, was obtained. They display better ER performance. The shear stress of the suspension of Y4O （OH）9 （NO3） （ NH4NO3 ）2.8 material in dimethyl silicone oil reaches 1469 Pa at an electric field strength （E） of 4.2 kV·mm^-1 and the shear rate （7） of 150 s^-1 The relative shear stress, τ E/τ0（ τE and τ0 are the shear stresses at E = 4.2 and 0 kV·mm^-1 respectively）, is up to 29, which is 19 times that of pure Y2O3 material. The dielectric and conductive property of the materials play important roles in the modification of the ER effect of the particle materials. The researches on these new ER materials are very useful for obtaining a better understanding on the mechanism of the ER effect and finding an ideal ER material.展开更多
The effect Of Y2O3 as additive to the positive electrode on the high-temperature performances of the Ni-MH batteries was studied. The specific capacities of the positive electrode in Ni-MH battery at higher temperatur...The effect Of Y2O3 as additive to the positive electrode on the high-temperature performances of the Ni-MH batteries was studied. The specific capacities of the positive electrode in Ni-MH battery at higher temperatures are much lower than usual. In order to improve high-temperature performances, charge/discharge curves of the Ni(OH)(2) electrodes with different amounts Of Y2O3 it different temperatures were studied. It is found that the specific capacities of the spherical Ni (OH)(2) with Y2O3 as additive are much higher than those of the regular at higher temperatures. The specific capacity of Ni (OH)(2) containing 1% Y2O3 at 0.2C C/D rate is 35% higher than that of the regular. The specific capacity of Ni (OH)(2) containing 0.2% Y2O3 at 1C C/D rate is 15% higher than that of the regular. Mechanism Of Y2O3 improving high temperature performances of Ni(OH)(2) electrode was also discussed in detail.展开更多
The purpose of this work is to synthesize the catalytic systems containing palladium nanoparticles and using hydroxycarbonates of yttrium and cerium as supports,and to test the catalytic activity of the obtained catal...The purpose of this work is to synthesize the catalytic systems containing palladium nanoparticles and using hydroxycarbonates of yttrium and cerium as supports,and to test the catalytic activity of the obtained catalysts in the Suzuki cross-couping reaction.Nanocomposites Pd/Y(OH)CO 3 and Pd/Ce(OH)CO 3 were synthesized according to two methods:the first one-simultaneous production of nanoscale substrate and immobilization of palladium nanoparticles on its surface(nanocomposites 1),the second one-the prior synthesis of polyvinylpyrrolidone stabilized palladium nanoparticles followed by their immobilization on the nano sized substrate surface(nanocomposites 2).The reaction between phenylboronic acid and iodobenzene is chosen as a model one.The dependence of the catalytic activity of catalysts on the method of their synthesis was established.It was established that nanocomposites 2 exhibit higher catalytic activity in the selected reaction compared to the nanocomposites 1.The TOF values for the nanocomposites 1 are 6663～14617 h 1 when using the substrate Ce(OH)CO 3 and 13774～27084 h 1 when using the substrate Y(OH)CO 3,while the nanocomposites 2 reveal TOF = 87287 h 1 for the substrate Ce(OH)CO 3 and TOF = 97746 h 1 for the substrate Y(OH)CO 3 under other equal conditions.In addition,nanocomposites 2 "work" at room temperature giving a high yield of the desired product.It is noted that the support nanoparticles Y(OH)CO 3 and Ce(OH)CO 3 also exhibit catalytic activity.The yield of the final product of the reaction using them as catalysts is 55%(TOF = 11 and 8 h 1,respectively).Thus,the use of yttrium and cerium hydroxycarbonates as supports allows to decrease the palladium content in the nanocomposites to 0.01%～1% and,consequently,reduce the cost of the catalyst while maintaining its high catalytic activity.展开更多
A series of thermodynamic parameters in formation of ultrafine monodispersed colloidal particles of Y(OH)CO3 were measured, estimated and calculated. The thermodynamic stability of Y(OH)CO3 colloidal particles was stu...A series of thermodynamic parameters in formation of ultrafine monodispersed colloidal particles of Y(OH)CO3 were measured, estimated and calculated. The thermodynamic stability of Y(OH)CO3 colloidal particles was studied and discussed by phenomenological model. It is suggested that ultrafine monodispersed colloidal particles of Y(OH)CO3 are stable only in a very narrow temporary supersaturation range ( 1<x<1 .08).展开更多
Ultrafine Y（OH）3 nanoparticles were successfully deposited from an additive-free 0.005 mol/L YCl3 low-temperature bath on the steel cathode at the current density of 0.5 mA/cm2 and bath temperature of 10 oC. Heat tr...Ultrafine Y（OH）3 nanoparticles were successfully deposited from an additive-free 0.005 mol/L YCl3 low-temperature bath on the steel cathode at the current density of 0.5 mA/cm2 and bath temperature of 10 oC. Heat treatment of the prepared Y（OH）3 nanoparticles at 600 oC in air led to the formation of Y2O3 nanoparticles. Thermal behavior and phase transformation during the heat treatment of Y（OH）3 were investigated by differential scanning calorimetry （DSC） and thermogramimetric analysis （TGA）. The morphologies, crystal structures and compositions of the prepared materials were examined by means of scanning and transmission electron microscopy （SEM and TEM） as well as X-ray diffraction （XRD） and FT-IR spectroscopy. The results showed that the prepared Y（OH）3 nanoparticles was essentially amorphous and composed of well dispersed ultrafine particles with size of 4 nm. After heat treatment, the obtained oxide product was well crystallized cubic phase of Y2O3 nanoparticles with the grain size of around 5 nm. It was concluded that low-temperature cathodic electrodeposition offered a facile and feasible way for preparation of ultrafine Y（OH）3 and Y2O3 nanoparticles.展开更多
基金supported by the Innovation Foundation of BUAA for Ph. D Graduates Provided by Beihang University in China
文摘This work focused on the zinc powder coated with Y(OH)3 microparticles by means of ultrasonic immersion for performance improvement of zinc electrodes in alkaline battery systems.Scanning electron microscopy and other characterization techniques were applied to examine the influence of the ultrasonic power on the sonochemical growth of Y(OH)3 microparticles in direct contact with zinc powder.Electrochemical properties of zinc electrodes containing Y(OH)3 microparticles were discussed through the measurement...
基金Program for Changjiang Scholars and Innovative Research Team in University (IRT0730)Chinese Ministry of Education Foundation for Core Young Teacher at University (GG-430-10403-1970)+1 种基金the Key Project of Department of Science and Technology of Jiangxi ProvinceProject of Education Department of Jiangxi
文摘The phase and morphology transformation during the hydrothermal treating process of Y2O3 was evaluated with X-ray difference (XRD), scanning electron microscopy (SEM), transmission electron microscopy (TEM), particle size and specific surface area determination. The results showed that the cubic Y2O3 did not transfer into hexagonal Y(OH)3 in pure water. Therefore, pure hexagonal Y(OH)3 with nanotube and microrod morphologies were obtained by hydrothermal treating Y2O3 at 150 oC for 12 h in 15 ml of 2 mol/L NaOH solution with and without PVA or PEG. It was suggested that the characteristic preferential growth of Y(OH)3 was attributed to the structure anisotropy of hexahedron Y(OH)3. The addition of PVA or PEG could promote the forming process of nanotubes by selective adsorption on different crystal planes, which altered the growth rate along different directions and resulted in the diffusion limit of constructing ions in the center top of rods. Finally, Y(OH)3:Eu and Y2O3:Eu nanotubes were also synthesized by using this method, and their photoluminescence properties were evaluated.
文摘The new electrorheologicai （ER） material, a particle material composed of Y4O（OH）9（NO3） and NH4NO3, was obtained. They display better ER performance. The shear stress of the suspension of Y4O （OH）9 （NO3） （ NH4NO3 ）2.8 material in dimethyl silicone oil reaches 1469 Pa at an electric field strength （E） of 4.2 kV·mm^-1 and the shear rate （7） of 150 s^-1 The relative shear stress, τ E/τ0（ τE and τ0 are the shear stresses at E = 4.2 and 0 kV·mm^-1 respectively）, is up to 29, which is 19 times that of pure Y2O3 material. The dielectric and conductive property of the materials play important roles in the modification of the ER effect of the particle materials. The researches on these new ER materials are very useful for obtaining a better understanding on the mechanism of the ER effect and finding an ideal ER material.
文摘The effect Of Y2O3 as additive to the positive electrode on the high-temperature performances of the Ni-MH batteries was studied. The specific capacities of the positive electrode in Ni-MH battery at higher temperatures are much lower than usual. In order to improve high-temperature performances, charge/discharge curves of the Ni(OH)(2) electrodes with different amounts Of Y2O3 it different temperatures were studied. It is found that the specific capacities of the spherical Ni (OH)(2) with Y2O3 as additive are much higher than those of the regular at higher temperatures. The specific capacity of Ni (OH)(2) containing 1% Y2O3 at 0.2C C/D rate is 35% higher than that of the regular. The specific capacity of Ni (OH)(2) containing 0.2% Y2O3 at 1C C/D rate is 15% higher than that of the regular. Mechanism Of Y2O3 improving high temperature performances of Ni(OH)(2) electrode was also discussed in detail.
文摘The purpose of this work is to synthesize the catalytic systems containing palladium nanoparticles and using hydroxycarbonates of yttrium and cerium as supports,and to test the catalytic activity of the obtained catalysts in the Suzuki cross-couping reaction.Nanocomposites Pd/Y(OH)CO 3 and Pd/Ce(OH)CO 3 were synthesized according to two methods:the first one-simultaneous production of nanoscale substrate and immobilization of palladium nanoparticles on its surface(nanocomposites 1),the second one-the prior synthesis of polyvinylpyrrolidone stabilized palladium nanoparticles followed by their immobilization on the nano sized substrate surface(nanocomposites 2).The reaction between phenylboronic acid and iodobenzene is chosen as a model one.The dependence of the catalytic activity of catalysts on the method of their synthesis was established.It was established that nanocomposites 2 exhibit higher catalytic activity in the selected reaction compared to the nanocomposites 1.The TOF values for the nanocomposites 1 are 6663～14617 h 1 when using the substrate Ce(OH)CO 3 and 13774～27084 h 1 when using the substrate Y(OH)CO 3,while the nanocomposites 2 reveal TOF = 87287 h 1 for the substrate Ce(OH)CO 3 and TOF = 97746 h 1 for the substrate Y(OH)CO 3 under other equal conditions.In addition,nanocomposites 2 "work" at room temperature giving a high yield of the desired product.It is noted that the support nanoparticles Y(OH)CO 3 and Ce(OH)CO 3 also exhibit catalytic activity.The yield of the final product of the reaction using them as catalysts is 55%(TOF = 11 and 8 h 1,respectively).Thus,the use of yttrium and cerium hydroxycarbonates as supports allows to decrease the palladium content in the nanocomposites to 0.01%～1% and,consequently,reduce the cost of the catalyst while maintaining its high catalytic activity.
文摘A series of thermodynamic parameters in formation of ultrafine monodispersed colloidal particles of Y(OH)CO3 were measured, estimated and calculated. The thermodynamic stability of Y(OH)CO3 colloidal particles was studied and discussed by phenomenological model. It is suggested that ultrafine monodispersed colloidal particles of Y(OH)CO3 are stable only in a very narrow temporary supersaturation range ( 1<x<1 .08).
文摘Ultrafine Y（OH）3 nanoparticles were successfully deposited from an additive-free 0.005 mol/L YCl3 low-temperature bath on the steel cathode at the current density of 0.5 mA/cm2 and bath temperature of 10 oC. Heat treatment of the prepared Y（OH）3 nanoparticles at 600 oC in air led to the formation of Y2O3 nanoparticles. Thermal behavior and phase transformation during the heat treatment of Y（OH）3 were investigated by differential scanning calorimetry （DSC） and thermogramimetric analysis （TGA）. The morphologies, crystal structures and compositions of the prepared materials were examined by means of scanning and transmission electron microscopy （SEM and TEM） as well as X-ray diffraction （XRD） and FT-IR spectroscopy. The results showed that the prepared Y（OH）3 nanoparticles was essentially amorphous and composed of well dispersed ultrafine particles with size of 4 nm. After heat treatment, the obtained oxide product was well crystallized cubic phase of Y2O3 nanoparticles with the grain size of around 5 nm. It was concluded that low-temperature cathodic electrodeposition offered a facile and feasible way for preparation of ultrafine Y（OH）3 and Y2O3 nanoparticles.
