A microwave-H202 process for sludge pretreatment exhibited high efticiencies of releasing organics, nitrogen, and phosphorus, but large quantifies of H202 residues were detected. A uniform design method was thus emplo...A microwave-H202 process for sludge pretreatment exhibited high efticiencies of releasing organics, nitrogen, and phosphorus, but large quantifies of H202 residues were detected. A uniform design method was thus employed in this study to further optimize H202 dosage by investigating effects of pH and H202 dosage on the amount of 1-I202 residue and releases of organics, nitrogen, and phosphorus. A regression model was established with pH and H202 dosage as the independent variables, and H202 residue and releases of organics, nitrogen, and phosphorus as the dependent variables. In the optimized microwave-H202 process, the pH value of the sludge was firstly adjusted to 11.0, then the sludge was heated to 80~C and H202 was dosed at a H202 ：mixed liquor suspended solids （MLSS） ratio of 0.2, and the sludge was finally heated to 100~C by microwave irradiation. Compared to the microwave-H202 process without optimization, the H202 dosage and the utilization rate of H202 in the optimized microwave-H202 process were reduced by 80% and greatly improved by 3.87 times, respectively, when the H202：MLSS dosage ratio was decreased from 1.0 to 0.2, resulting in nearly the same release rate of soluble chemical oxygen demand in the microwave-H202 process without optimization at H202：MLSS ratio of 0.5.展开更多
The non-grinding long afterglow material SrAl2O4：Eu^2＋ , Dy^3＋ was prepared by combustion method in home mierowave oven direetly, after dispersant, frother, eomburent, and mineralizer were added into the reacting s...The non-grinding long afterglow material SrAl2O4：Eu^2＋ , Dy^3＋ was prepared by combustion method in home mierowave oven direetly, after dispersant, frother, eomburent, and mineralizer were added into the reacting system. XRD analysis showed that the powders were nearly pure SrAl2O4 phase with few other phases, and the size of the grain was 41.1 nm. Fluoreseenee speetrum results indieated that there were 2 exeitation peaks loeated at 345 and 400 nm, and the emission peak loeated at 516 nm, afterglow lasted up to 30 min or more. The mierowave eombustion method has advantages of less time, low temperature and no grinding process, and the material made by the method has good luminescent property.展开更多
Blue-green luminescent BaAl2O4：Eu2＋,Dy3＋ phosphor powders were synthesized via combustion synthesis method assisted by microwave irradiation in air. The phosphors were characterized by X-ray diffraction （XRD）, sc...Blue-green luminescent BaAl2O4：Eu2＋,Dy3＋ phosphor powders were synthesized via combustion synthesis method assisted by microwave irradiation in air. The phosphors were characterized by X-ray diffraction （XRD）, scanning electron microscopy （SEM） and fluorescence spectrophotometer. The XRD results revealed that when the concentration of urea was over 3 times higher than theoretical quantities, a BaAl2O4 single hexagonal phase was obtained. The SEM results revealed that the surface of the BaAl2O4：Eu2＋,Dy3＋ powder samples showed lots of voids and pores. The BaAl2O4：Eu2＋,Dy3＋ phosphors exhibited a broad emission band of main peak at 496 nm and a shoulder peak at 426 nm under excitation of 337 nm. The BaAl2O4：Eu2＋,Dy3＋ phosphors at the Eu2＋ concentration of 1 mol.% showed the strongest luminescent intensity. Long afterglow phosphorescence was observed in the dark with naked eyes after the removal of the excitation source.展开更多
Novel red-emitting phosphors Sr2MgSi2O7：Eu3＋ were prepared by gel-combustion method assisted by microwave. The phase struc-ture and luminescent properties of as-synthesized phosphors were investigated by XRD and flu...Novel red-emitting phosphors Sr2MgSi2O7：Eu3＋ were prepared by gel-combustion method assisted by microwave. The phase struc-ture and luminescent properties of as-synthesized phosphors were investigated by XRD and fluorescence spectrophotometer, respectively. The results showed that the as-synthesized sample was Sr2MgSi2O7 with tetragonal crystal structure. The excitation spectrum of Sr2MgSi2O7：Eu3＋ was composed of two major parts： one was the broad band between 200 and 350 nm, which belonged to the charge transfer of Eu3＋-O2-; the other consisted of a series of sharp lines between 350 and 450 nm, ascribed to the f-f transition of Eu3＋. The emission spec-trum consisted of two emission peaks at 593 and 616 nm, which was attributed to 5D0→7F1 and 5D0→7F2 of Eu3＋, respectively. The concen-tration of Eu3＋ （x） had great effect on the emission intensity of Sr2-xMgSi2O7：Eu3＋x. When x varied in the range of 0.04-0.18, the intensity of emission peaks at 593 and 616 nm increased gradually with the concentration of Eu3＋ increasing. It was interesting that no concentration quenching occurred. Moreover, the luminescent intensity could be greatly enhanced with incorporation of charge compensator Li＋ ions.展开更多
The ternary transitional metal oxide NiCo_2O_4 is a promising anode material for sodium ion batteries due to its high theoretical capacity and superior electrical conductivity. However, its sodium storage capability i...The ternary transitional metal oxide NiCo_2O_4 is a promising anode material for sodium ion batteries due to its high theoretical capacity and superior electrical conductivity. However, its sodium storage capability is severely limited by the sluggish sodiation/desodiation reaction kinetics. Herein, NiCo_2O_4 double-shelled hollow spheres were synthesized via a microwave-assisted, fast solvothermal synthetic procedure in a mixture of isopropanol and glycerol, followed by annealing. Isopropanol played a vital role in the precipitation of nickel and cobalt,and the shrinkage of the glycerol quasi-emulsion under heat treatment was responsible for the formation of the double-shelled nanostructure. The as-synthesized productwas tested as an anode material in a sodium ion battery,was found to exhibit a high reversible specific capacity of 511 m Ahg^(-1) at 100 m Ag^(-1), and deliver high capacity retention after 100 cycles.展开更多
BaO-Sm2O3-TiO2 microwave dielectric ceramics doped with Bi and Zn was studied. The experiment was based on BST microwave dielectric ceramics doped with Bi2O3, which is shown by Ba4(Sm1-yBiy )28/3Ti18O54. When y =0.15,...BaO-Sm2O3-TiO2 microwave dielectric ceramics doped with Bi and Zn was studied. The experiment was based on BST microwave dielectric ceramics doped with Bi2O3, which is shown by Ba4(Sm1-yBiy )28/3Ti18O54. When y =0.15, ZnO was added and the effects of ZnO on this system were studied. The result shows that the dielectric characteristics of BST microwave dielectric ceramics are the most excellent when the content of ZnO is 3% , and the optimal sintering temperature is 1200℃.展开更多
The present paper reported the structural and luminescent properties of Eu^（2＋） and Nd^（3＋） doped CaAl_2O_4 phosphor. The samples were prepared by microwave-assisted chemical co-precipitation（MA-CCP）, a synthe...The present paper reported the structural and luminescent properties of Eu^（2＋） and Nd^（3＋） doped CaAl_2O_4 phosphor. The samples were prepared by microwave-assisted chemical co-precipitation（MA-CCP）, a synthesis technique which is suitable for small and uniform particle that could be used directly without grinding. The effects of different microwave temperatures on structure and photoluminescence behavior were studied. Formation of a phosphor and phase purity were confirmed by X-ray diffraction technique（XRD） with variable microwave temperatures. XRD analysis showed that the phosphors prepared by MA-CCP method at the temperature of 750, 900oC, respectively and solid-state reaction（SSR） method at 1300oC consisted of impurities. Commission Internationale de L＇Eclairage（CIE） color coordinates of CaAl_2O_4：Eu^（2＋）,Nd^（3＋） were suitable as blue light emitting phosphor. Excitation and emission peaks of the samples prepared by different methods in this study were almost the same. The images of SEM showed that the size of the phosphors prepared by MA-CCP method reached a submicrometer.展开更多
The effect of Sn^4＋ （BaSnO3） B-site substitution on the microstructure and dielectric properties of Ba（Mg1/3Ta2/3）O3 microwave ceramics was investigated. X-ray diffraction shows that a complex perovskite material...The effect of Sn^4＋ （BaSnO3） B-site substitution on the microstructure and dielectric properties of Ba（Mg1/3Ta2/3）O3 microwave ceramics was investigated. X-ray diffraction shows that a complex perovskite material Ba（Mg1/3Ta2/3）O3 was prepared. As Sn^4＋ content x increases in the （1-x） Ba（Mg1/3Ta2/3）O3-xBaSnO3 （x=0.00～0.20） system, the dielectric constant generally keeps unchanged, while TCF changes from positive to negative. Although the addition of Sn^4＋ reduces the ordering degree, Q f0 is still increased when the ceramics density increases. This trend implies that Q f0 of this system is mostly determined by ceramics density rather than ordering degree. After sintering at 1500℃ for 3 h, the system with x=0.15 was found to have excellent dielectric properties as follows：ε≈25, Q f0≥300,000 GHz at 7 GHz, TCF=-0.6×10^-6/℃.展开更多
We fabricated YBa2Cu3O7–d bulk ceramics with a domestic microwave oven and investigated the effect of pressure at the press procedure. If the pressure was not high enough, the ratio of BaCuO2 phase became large, esti...We fabricated YBa2Cu3O7–d bulk ceramics with a domestic microwave oven and investigated the effect of pressure at the press procedure. If the pressure was not high enough, the ratio of BaCuO2 phase became large, estimated from x-ray diffraction (XRD) measurements. We found that the pressure should be 700 kgf/cm2 at least in order to suppress the BaCuO2 phase.展开更多
This article shows main principles and presents ideas described in the scientific and technical literature, on the mechanism of interaction of microwave radiation with a solid phase materials, which were used as a bas...This article shows main principles and presents ideas described in the scientific and technical literature, on the mechanism of interaction of microwave radiation with a solid phase materials, which were used as a basis of creation of new perspective, energy efficient and environmentally safe technologies of preparation of heterogeneous catalysts for the reactions which were carried out under the influence of electro-magnetic radiation of microwave radiation. Author’s research results confirm possibilities of practical use of proposed method of hydrothermal oxidation of industrial low-dispersing of aluminum powders with presence of bulk phase of Al(ОН)<sub>3</sub>·nH<sub>2</sub>O, with further thermal treatment in microwave field for acquisition of armored А1/А1<sub>2</sub>О3<sub>3</sub> compositions, which effectively consume energy of microwave radiation. Due to the textured characteristics and thermo-transforming ability, synthesized components can be used as potential universal bearings of catalysts for reactions stimulated by electromagnetic radiation of (2.45 GHz) microwave frequency.展开更多
In this context,the present study proposes the use of microwave irradiation to improve the dehydration rate and efficiency of strontium hydroxide octahydrate(Sr(OH)_(2)·8H_(2)O)without introducing contaminants.Th...In this context,the present study proposes the use of microwave irradiation to improve the dehydration rate and efficiency of strontium hydroxide octahydrate(Sr(OH)_(2)·8H_(2)O)without introducing contaminants.This study revealed that the use of microwave irradiation to dehydrate Sr(OH)_(2)·8H_(2)O is feasible and surprisingly efficient.The effects of this approach on important parameters were investigated using response surface methodology(RSM).The results revealed that the microwave dehydration process follows a linear polynomial model.In addition,compared with the heating time and material thickness,the microwave-assisted dehydration of Sr(OH)_(2)·8H_(2)O is sensitive to the microwave power and not to the material mass.The relative dehydration percentage reached 99.99%when heated in a microwave oven at 950Wfor just 3 min.In contrast,a relative dehydration percentage of 94.6%was reached when heated in an electric furnace at 180℃for 120 min.The XRD spectra also revealed that most of the Sr(OH)_(2)·8H_(2)O transformed into Sr(OH)_(2)after dehydration via microwave irradiation,whereas a significant portion of the Sr(OH)_(2)·H_(2)O remained after conventional electric dehydration.The experimental data were fitted and analyzed via the thin-layer drying dynamics model,and the results indicated that the dehydrating behavior of Sr(OH)_(2)·8H_(2)O could be well described by the Page model.展开更多
The integration of selective oxidation of renewable biomass and its derivatives with hydrogen(H_(2))pro-duction holds significant potential for simultaneously yielding value-added chemicals and“green H_(2)”,contribu...The integration of selective oxidation of renewable biomass and its derivatives with hydrogen(H_(2))pro-duction holds significant potential for simultaneously yielding value-added chemicals and“green H_(2)”,contributing to addressing sustainability challenges.The S-scheme charge transfer mechanism enhances charge separation by maintaining strong redox potentials at both ends,facilitating both oxidation and reduction reactions.Herein,we synthesize a visible-light-responsive oxygen vacancy-rich In_(2)O_(3-x)/tubular carbon nitride(IO_(OV)/TCN)S-scheme heterojunction photocatalyst via electrostatic adherence for selec-tive 5-hydroxymethylfurfural(HMF)oxidation to 2,5-diformylfuran(DFF)and 2,5-furandicarboxylic acid(FDCA),alongside H_(2)production.Under anaerobic conditions and visible-light irradiation,the optimal IOOV/TCN-10 catalyst achieves an HMF conversion of 94.8%with a selectivity of 53.6%for DFF and FDCA,and a H_(2)yield of 754.05μmol g^(−1)in 3 h.The significantly improved photocatalytic activity results from enhanced visible-light absorption,reduced carrier recombination,and abundant catalytic active sites due to the synergistic effect of surface oxygen vacancies,the hollow nanotube-based architecture,and the S-scheme charge transfer mechanism.This work highlights the great potentials of S-scheme heterojunctions in biomass conversion for sustainable energy use and chemical production.展开更多
The problem of water and sulfur poisoning in flue gas atmosphere remains a significant obstacle for low-temperature deNO_(x) catalysts.This study investigated the sulfation mechanism of the CoMn_(2)O_(4)/CeTiO_(x)(CMC...The problem of water and sulfur poisoning in flue gas atmosphere remains a significant obstacle for low-temperature deNO_(x) catalysts.This study investigated the sulfation mechanism of the CoMn_(2)O_(4)/CeTiO_(x)(CMCT)catalyst during the selective catalytic reduction of NO_(x) with NH3 under conditions containing H2O and SO_(2) at 150℃.Employing a comprehensive suite of time-resolved analysis and characterization techniques,the evolution of sulfate species was systematically categorized into three stages:initial rapid surface sulfate accumulation,the transformation of surface sulfates to bulk metal sulfates,and partial sulfates decomposition after the removal of H2O and SO_(2).These findings indicate that bulk metal sulfates irreversibly deactivate the catalyst by distorting active component lattices and consuming oxygen vacancies,whereas surface sulfates(including ammonium sulfates and surface-coordinated metal sulfates)cause reversible performance loss through decomposition.Furthermore,the competitive adsorption of H2O and SO_(2) significantly influences the catalytic efficiency,with H2O suppressing SO_(2) adsorption while simultaneously enhancing the formation of Brönsted acid sites.This research underscores the critical role of sulfate dynamics on catalyst performance,revealing the enhanced SO_(2) resistance of the Eley-Rideal mechanism facilitated by the Ce-Ti support relative to the Langmuir-Hinshelwood pathway.Collectively,the study unravels the complex interplay of sulfate dynamics influencing catalyst performance and provides potential approaches to mitigate deactivation in demanding atmospheric conditions.展开更多
Steel-cemented WC was prepared by ball milling, cold compacting and microwave sintering with Fe powder as the matrix, WC as the hard phase and the addition of rare earth Y2O3. The results show that the interface of th...Steel-cemented WC was prepared by ball milling, cold compacting and microwave sintering with Fe powder as the matrix, WC as the hard phase and the addition of rare earth Y2O3. The results show that the interface of the WC particles and Fe matrix exhibits excellent wettability and liquidity when the microwave sintering temperature reaches 1,280℃. The density and mechanical properties of the steel bonded WC carbides could be greatly improved, the hard phases become finer and more uniform dispersed owing to the addition of Y2O3. With the increase of the Y2O3 contents, the grain becomes uniform and fine first, and then gathers and grows up. The relative density, microhardness and bending strength all rise first, reaching the maximum values of 97.29 %, HV1024 and 1,267.60 MPa at 0.5 % Y2O3, respectively, and then decrease. Moreover, the relative density and mechanical properties of the steel-cemented WC with nano-Y2O3 are higher than that with micron-Y2O3, which indicates that the effect of nano-Y2O3 is better than that of the micron-Y2O3.展开更多
Ni(Co/Zn/Cu)Fe_2O_4/SiC@SiO_2, a microwave absorber, was prepared by the sol-gel method. The phase structure and the morphology of the microwave absorbers were characterized by X-Ray Diffraction(XRD) and scanning elec...Ni(Co/Zn/Cu)Fe_2O_4/SiC@SiO_2, a microwave absorber, was prepared by the sol-gel method. The phase structure and the morphology of the microwave absorbers were characterized by X-Ray Diffraction(XRD) and scanning electron microscopy(SEM), respectively. Laser sizer(LS) and X-ray photoelectron spectroscopy(XPS) analysis show the core-shell structure of SiC@SiO_2. Coaxial method was used to measure the microwave absorption properties of the prepared composites in the frequency range of 2-18 GHz. When 70 wt% SiC is wrapped by 30 wt% SiO_2,and 50 wt% NiFe_2O_4 is added into 50 wt% SiC@SiO_2, the as-prepared powders are found to have advanced microwave absorption properties with a minimum reflection loss(RL) of -32.26 dB at about 6.08 GHz, and the available bandwidth is approximately 2.1 GHz when the RL is below -10 dB.展开更多
Fe_(0.64)Ni_(0.36)-NiFe_2O_4 nanocomposite was performed with partially reducing NiFe_2O_4 nanoparticles in Ar/H_2 ambient.The microwave and static magnetic properties were investigated.The results showed that the nan...Fe_(0.64)Ni_(0.36)-NiFe_2O_4 nanocomposite was performed with partially reducing NiFe_2O_4 nanoparticles in Ar/H_2 ambient.The microwave and static magnetic properties were investigated.The results showed that the nanocomposite was characterized with enhanced microwave absorption properties.The optimal reflection loss(RL)of the nanocomposite reached-24.8 dB at 14 GHz for an absorber thickness of 1.5 mm.Meanwhile,a broad bandwidth for RL<-10 dB was obtained in the range of 3.1—15.1 GHz for an absorber thickness from1.0 to 4.0 mm.The enhancement is attributed to the increase of dielectric and magnetic loss after reducing procedure.展开更多
A facile and cheap method for the fabrication of WC-Al2O3composite powder was proposed.Thermodynamic calculations indicate that aluminothermic reduction of WO3in WO3:xAl:(4-1.5x)C mixture is accompanied by a great dea...A facile and cheap method for the fabrication of WC-Al2O3composite powder was proposed.Thermodynamic calculations indicate that aluminothermic reduction of WO3in WO3:xAl:(4-1.5x)C mixture is accompanied by a great deal of heat,so carbothermic reduction reaction(endothermic)becomes activated in the system.By substitution of aluminum with carbon,the formation of unwanted W2C phase can be prevented because of less thermodynamic stability at lower temperatures.For the verification of the proposed reaction mechanism,various WO3:xAl:(4-1.5x)C mixtures(1.1≤x≤2)were heat-treated in a domestic microwave oven.The results showed that the type of reaction is self-propagating high temperature synthesis(SHS)when1.4≤x≤2.Lower amount of Al in WO3:xAl:(4-1.5x)C mixtures results in a higher formation of WC.A W2C-free WC-Al2O3composite was obtained by continuation of microwave heating in an isolated atmosphere,after the occurrence of SHS reaction in a mixture containing1.4mol of Al.Results also showed that when x≤1.3,type of reaction becomes gradual,which in turn brings about the incompleteness reaction and residue of initial reagents.展开更多
基金supported by the National Natural Science Foundation of China (No. 51008297)the Hi-Tech Research and Development Program (863) of China(No. 2007AA06Z347)the National Major Science & Technology Projects for Water Pollution Control and Management (No. 2012ZX07202-005)
文摘A microwave-H202 process for sludge pretreatment exhibited high efticiencies of releasing organics, nitrogen, and phosphorus, but large quantifies of H202 residues were detected. A uniform design method was thus employed in this study to further optimize H202 dosage by investigating effects of pH and H202 dosage on the amount of 1-I202 residue and releases of organics, nitrogen, and phosphorus. A regression model was established with pH and H202 dosage as the independent variables, and H202 residue and releases of organics, nitrogen, and phosphorus as the dependent variables. In the optimized microwave-H202 process, the pH value of the sludge was firstly adjusted to 11.0, then the sludge was heated to 80~C and H202 was dosed at a H202 ：mixed liquor suspended solids （MLSS） ratio of 0.2, and the sludge was finally heated to 100~C by microwave irradiation. Compared to the microwave-H202 process without optimization, the H202 dosage and the utilization rate of H202 in the optimized microwave-H202 process were reduced by 80% and greatly improved by 3.87 times, respectively, when the H202：MLSS dosage ratio was decreased from 1.0 to 0.2, resulting in nearly the same release rate of soluble chemical oxygen demand in the microwave-H202 process without optimization at H202：MLSS ratio of 0.5.
基金Project supported by the National Natural Science Foundation of China (20476002)
文摘The non-grinding long afterglow material SrAl2O4：Eu^2＋ , Dy^3＋ was prepared by combustion method in home mierowave oven direetly, after dispersant, frother, eomburent, and mineralizer were added into the reacting system. XRD analysis showed that the powders were nearly pure SrAl2O4 phase with few other phases, and the size of the grain was 41.1 nm. Fluoreseenee speetrum results indieated that there were 2 exeitation peaks loeated at 345 and 400 nm, and the emission peak loeated at 516 nm, afterglow lasted up to 30 min or more. The mierowave eombustion method has advantages of less time, low temperature and no grinding process, and the material made by the method has good luminescent property.
基金supported by the National Natural Science Foundation of China (60477034)
文摘Blue-green luminescent BaAl2O4：Eu2＋,Dy3＋ phosphor powders were synthesized via combustion synthesis method assisted by microwave irradiation in air. The phosphors were characterized by X-ray diffraction （XRD）, scanning electron microscopy （SEM） and fluorescence spectrophotometer. The XRD results revealed that when the concentration of urea was over 3 times higher than theoretical quantities, a BaAl2O4 single hexagonal phase was obtained. The SEM results revealed that the surface of the BaAl2O4：Eu2＋,Dy3＋ powder samples showed lots of voids and pores. The BaAl2O4：Eu2＋,Dy3＋ phosphors exhibited a broad emission band of main peak at 496 nm and a shoulder peak at 426 nm under excitation of 337 nm. The BaAl2O4：Eu2＋,Dy3＋ phosphors at the Eu2＋ concentration of 1 mol.% showed the strongest luminescent intensity. Long afterglow phosphorescence was observed in the dark with naked eyes after the removal of the excitation source.
基金Project supported by the National Natural Science Foundation of China (20675023)
文摘Novel red-emitting phosphors Sr2MgSi2O7：Eu3＋ were prepared by gel-combustion method assisted by microwave. The phase struc-ture and luminescent properties of as-synthesized phosphors were investigated by XRD and fluorescence spectrophotometer, respectively. The results showed that the as-synthesized sample was Sr2MgSi2O7 with tetragonal crystal structure. The excitation spectrum of Sr2MgSi2O7：Eu3＋ was composed of two major parts： one was the broad band between 200 and 350 nm, which belonged to the charge transfer of Eu3＋-O2-; the other consisted of a series of sharp lines between 350 and 450 nm, ascribed to the f-f transition of Eu3＋. The emission spec-trum consisted of two emission peaks at 593 and 616 nm, which was attributed to 5D0→7F1 and 5D0→7F2 of Eu3＋, respectively. The concen-tration of Eu3＋ （x） had great effect on the emission intensity of Sr2-xMgSi2O7：Eu3＋x. When x varied in the range of 0.04-0.18, the intensity of emission peaks at 593 and 616 nm increased gradually with the concentration of Eu3＋ increasing. It was interesting that no concentration quenching occurred. Moreover, the luminescent intensity could be greatly enhanced with incorporation of charge compensator Li＋ ions.
基金financially supported by the Science Foundation of Sichuan Province(Grant No.2016FZ0070)the Natural Science Foundation of China(NSFC,201476145)the technical support for Materials Characterization from The Analytical and Testing Center of Sichuan University
文摘The ternary transitional metal oxide NiCo_2O_4 is a promising anode material for sodium ion batteries due to its high theoretical capacity and superior electrical conductivity. However, its sodium storage capability is severely limited by the sluggish sodiation/desodiation reaction kinetics. Herein, NiCo_2O_4 double-shelled hollow spheres were synthesized via a microwave-assisted, fast solvothermal synthetic procedure in a mixture of isopropanol and glycerol, followed by annealing. Isopropanol played a vital role in the precipitation of nickel and cobalt,and the shrinkage of the glycerol quasi-emulsion under heat treatment was responsible for the formation of the double-shelled nanostructure. The as-synthesized productwas tested as an anode material in a sodium ion battery,was found to exhibit a high reversible specific capacity of 511 m Ahg^(-1) at 100 m Ag^(-1), and deliver high capacity retention after 100 cycles.
文摘BaO-Sm2O3-TiO2 microwave dielectric ceramics doped with Bi and Zn was studied. The experiment was based on BST microwave dielectric ceramics doped with Bi2O3, which is shown by Ba4(Sm1-yBiy )28/3Ti18O54. When y =0.15, ZnO was added and the effects of ZnO on this system were studied. The result shows that the dielectric characteristics of BST microwave dielectric ceramics are the most excellent when the content of ZnO is 3% , and the optimal sintering temperature is 1200℃.
基金Project supported by the Fundamental Research Funds for the Central Universities(JUSRP51723B)National Natural Science Foundation of China(51503083)+2 种基金Jiangsu Province Ordinary University Academic Degree Graduate Student Scientific Research Innovation Projects(KYLX16_0798)the Priority Academic Program Development of Jiangsu Higher Education InstitutionsProduction,Education&Research Cooperative Innovation Fund Project of Jiangsu Province(BY2015057-23)
文摘The present paper reported the structural and luminescent properties of Eu^（2＋） and Nd^（3＋） doped CaAl_2O_4 phosphor. The samples were prepared by microwave-assisted chemical co-precipitation（MA-CCP）, a synthesis technique which is suitable for small and uniform particle that could be used directly without grinding. The effects of different microwave temperatures on structure and photoluminescence behavior were studied. Formation of a phosphor and phase purity were confirmed by X-ray diffraction technique（XRD） with variable microwave temperatures. XRD analysis showed that the phosphors prepared by MA-CCP method at the temperature of 750, 900oC, respectively and solid-state reaction（SSR） method at 1300oC consisted of impurities. Commission Internationale de L＇Eclairage（CIE） color coordinates of CaAl_2O_4：Eu^（2＋）,Nd^（3＋） were suitable as blue light emitting phosphor. Excitation and emission peaks of the samples prepared by different methods in this study were almost the same. The images of SEM showed that the size of the phosphors prepared by MA-CCP method reached a submicrometer.
文摘The effect of Sn^4＋ （BaSnO3） B-site substitution on the microstructure and dielectric properties of Ba（Mg1/3Ta2/3）O3 microwave ceramics was investigated. X-ray diffraction shows that a complex perovskite material Ba（Mg1/3Ta2/3）O3 was prepared. As Sn^4＋ content x increases in the （1-x） Ba（Mg1/3Ta2/3）O3-xBaSnO3 （x=0.00～0.20） system, the dielectric constant generally keeps unchanged, while TCF changes from positive to negative. Although the addition of Sn^4＋ reduces the ordering degree, Q f0 is still increased when the ceramics density increases. This trend implies that Q f0 of this system is mostly determined by ceramics density rather than ordering degree. After sintering at 1500℃ for 3 h, the system with x=0.15 was found to have excellent dielectric properties as follows：ε≈25, Q f0≥300,000 GHz at 7 GHz, TCF=-0.6×10^-6/℃.
文摘We fabricated YBa2Cu3O7–d bulk ceramics with a domestic microwave oven and investigated the effect of pressure at the press procedure. If the pressure was not high enough, the ratio of BaCuO2 phase became large, estimated from x-ray diffraction (XRD) measurements. We found that the pressure should be 700 kgf/cm2 at least in order to suppress the BaCuO2 phase.
文摘This article shows main principles and presents ideas described in the scientific and technical literature, on the mechanism of interaction of microwave radiation with a solid phase materials, which were used as a basis of creation of new perspective, energy efficient and environmentally safe technologies of preparation of heterogeneous catalysts for the reactions which were carried out under the influence of electro-magnetic radiation of microwave radiation. Author’s research results confirm possibilities of practical use of proposed method of hydrothermal oxidation of industrial low-dispersing of aluminum powders with presence of bulk phase of Al(ОН)<sub>3</sub>·nH<sub>2</sub>O, with further thermal treatment in microwave field for acquisition of armored А1/А1<sub>2</sub>О3<sub>3</sub> compositions, which effectively consume energy of microwave radiation. Due to the textured characteristics and thermo-transforming ability, synthesized components can be used as potential universal bearings of catalysts for reactions stimulated by electromagnetic radiation of (2.45 GHz) microwave frequency.
基金supported by the Research Program of the Science and Technology Department of Guizhou Province(Qiankehe Jichu[2019]1418)the Research Program of Talented Scholars of Guizhou Institute of Technology(XJGC20190965).
文摘In this context,the present study proposes the use of microwave irradiation to improve the dehydration rate and efficiency of strontium hydroxide octahydrate(Sr(OH)_(2)·8H_(2)O)without introducing contaminants.This study revealed that the use of microwave irradiation to dehydrate Sr(OH)_(2)·8H_(2)O is feasible and surprisingly efficient.The effects of this approach on important parameters were investigated using response surface methodology(RSM).The results revealed that the microwave dehydration process follows a linear polynomial model.In addition,compared with the heating time and material thickness,the microwave-assisted dehydration of Sr(OH)_(2)·8H_(2)O is sensitive to the microwave power and not to the material mass.The relative dehydration percentage reached 99.99%when heated in a microwave oven at 950Wfor just 3 min.In contrast,a relative dehydration percentage of 94.6%was reached when heated in an electric furnace at 180℃for 120 min.The XRD spectra also revealed that most of the Sr(OH)_(2)·8H_(2)O transformed into Sr(OH)_(2)after dehydration via microwave irradiation,whereas a significant portion of the Sr(OH)_(2)·H_(2)O remained after conventional electric dehydration.The experimental data were fitted and analyzed via the thin-layer drying dynamics model,and the results indicated that the dehydrating behavior of Sr(OH)_(2)·8H_(2)O could be well described by the Page model.
基金financially supported by the Natural Science Foundation of China(Nos.21972058,22102064,and 22302080)Anhui Key Laboratory of Nanomaterials and Nanotechnology,the Major Science and Technology Projects in Anhui Province(No.202305a12020006).
文摘The integration of selective oxidation of renewable biomass and its derivatives with hydrogen(H_(2))pro-duction holds significant potential for simultaneously yielding value-added chemicals and“green H_(2)”,contributing to addressing sustainability challenges.The S-scheme charge transfer mechanism enhances charge separation by maintaining strong redox potentials at both ends,facilitating both oxidation and reduction reactions.Herein,we synthesize a visible-light-responsive oxygen vacancy-rich In_(2)O_(3-x)/tubular carbon nitride(IO_(OV)/TCN)S-scheme heterojunction photocatalyst via electrostatic adherence for selec-tive 5-hydroxymethylfurfural(HMF)oxidation to 2,5-diformylfuran(DFF)and 2,5-furandicarboxylic acid(FDCA),alongside H_(2)production.Under anaerobic conditions and visible-light irradiation,the optimal IOOV/TCN-10 catalyst achieves an HMF conversion of 94.8%with a selectivity of 53.6%for DFF and FDCA,and a H_(2)yield of 754.05μmol g^(−1)in 3 h.The significantly improved photocatalytic activity results from enhanced visible-light absorption,reduced carrier recombination,and abundant catalytic active sites due to the synergistic effect of surface oxygen vacancies,the hollow nanotube-based architecture,and the S-scheme charge transfer mechanism.This work highlights the great potentials of S-scheme heterojunctions in biomass conversion for sustainable energy use and chemical production.
文摘The problem of water and sulfur poisoning in flue gas atmosphere remains a significant obstacle for low-temperature deNO_(x) catalysts.This study investigated the sulfation mechanism of the CoMn_(2)O_(4)/CeTiO_(x)(CMCT)catalyst during the selective catalytic reduction of NO_(x) with NH3 under conditions containing H2O and SO_(2) at 150℃.Employing a comprehensive suite of time-resolved analysis and characterization techniques,the evolution of sulfate species was systematically categorized into three stages:initial rapid surface sulfate accumulation,the transformation of surface sulfates to bulk metal sulfates,and partial sulfates decomposition after the removal of H2O and SO_(2).These findings indicate that bulk metal sulfates irreversibly deactivate the catalyst by distorting active component lattices and consuming oxygen vacancies,whereas surface sulfates(including ammonium sulfates and surface-coordinated metal sulfates)cause reversible performance loss through decomposition.Furthermore,the competitive adsorption of H2O and SO_(2) significantly influences the catalytic efficiency,with H2O suppressing SO_(2) adsorption while simultaneously enhancing the formation of Brönsted acid sites.This research underscores the critical role of sulfate dynamics on catalyst performance,revealing the enhanced SO_(2) resistance of the Eley-Rideal mechanism facilitated by the Ce-Ti support relative to the Langmuir-Hinshelwood pathway.Collectively,the study unravels the complex interplay of sulfate dynamics influencing catalyst performance and provides potential approaches to mitigate deactivation in demanding atmospheric conditions.
基金supported by the Science and Technology Plan Projects of Jiangxi Province (No. 2011BBE50010)the Project from the Jiangxi Province Key Laboratory of Copper Tungsten New Materials (No. 2011-TW-08)
文摘Steel-cemented WC was prepared by ball milling, cold compacting and microwave sintering with Fe powder as the matrix, WC as the hard phase and the addition of rare earth Y2O3. The results show that the interface of the WC particles and Fe matrix exhibits excellent wettability and liquidity when the microwave sintering temperature reaches 1,280℃. The density and mechanical properties of the steel bonded WC carbides could be greatly improved, the hard phases become finer and more uniform dispersed owing to the addition of Y2O3. With the increase of the Y2O3 contents, the grain becomes uniform and fine first, and then gathers and grows up. The relative density, microhardness and bending strength all rise first, reaching the maximum values of 97.29 %, HV1024 and 1,267.60 MPa at 0.5 % Y2O3, respectively, and then decrease. Moreover, the relative density and mechanical properties of the steel-cemented WC with nano-Y2O3 are higher than that with micron-Y2O3, which indicates that the effect of nano-Y2O3 is better than that of the micron-Y2O3.
基金financially supported by the Military Project of the Ministry of National Defense of China (No. JPPT-125-2-168)
文摘Ni(Co/Zn/Cu)Fe_2O_4/SiC@SiO_2, a microwave absorber, was prepared by the sol-gel method. The phase structure and the morphology of the microwave absorbers were characterized by X-Ray Diffraction(XRD) and scanning electron microscopy(SEM), respectively. Laser sizer(LS) and X-ray photoelectron spectroscopy(XPS) analysis show the core-shell structure of SiC@SiO_2. Coaxial method was used to measure the microwave absorption properties of the prepared composites in the frequency range of 2-18 GHz. When 70 wt% SiC is wrapped by 30 wt% SiO_2,and 50 wt% NiFe_2O_4 is added into 50 wt% SiC@SiO_2, the as-prepared powders are found to have advanced microwave absorption properties with a minimum reflection loss(RL) of -32.26 dB at about 6.08 GHz, and the available bandwidth is approximately 2.1 GHz when the RL is below -10 dB.
基金supported by National Science Fund for Distinguished Young Scholars (Grant No.50925103)the National Nature Science Foundation of China (Grant No.11034004)
文摘Fe_(0.64)Ni_(0.36)-NiFe_2O_4 nanocomposite was performed with partially reducing NiFe_2O_4 nanoparticles in Ar/H_2 ambient.The microwave and static magnetic properties were investigated.The results showed that the nanocomposite was characterized with enhanced microwave absorption properties.The optimal reflection loss(RL)of the nanocomposite reached-24.8 dB at 14 GHz for an absorber thickness of 1.5 mm.Meanwhile,a broad bandwidth for RL<-10 dB was obtained in the range of 3.1—15.1 GHz for an absorber thickness from1.0 to 4.0 mm.The enhancement is attributed to the increase of dielectric and magnetic loss after reducing procedure.
文摘A facile and cheap method for the fabrication of WC-Al2O3composite powder was proposed.Thermodynamic calculations indicate that aluminothermic reduction of WO3in WO3:xAl:(4-1.5x)C mixture is accompanied by a great deal of heat,so carbothermic reduction reaction(endothermic)becomes activated in the system.By substitution of aluminum with carbon,the formation of unwanted W2C phase can be prevented because of less thermodynamic stability at lower temperatures.For the verification of the proposed reaction mechanism,various WO3:xAl:(4-1.5x)C mixtures(1.1≤x≤2)were heat-treated in a domestic microwave oven.The results showed that the type of reaction is self-propagating high temperature synthesis(SHS)when1.4≤x≤2.Lower amount of Al in WO3:xAl:(4-1.5x)C mixtures results in a higher formation of WC.A W2C-free WC-Al2O3composite was obtained by continuation of microwave heating in an isolated atmosphere,after the occurrence of SHS reaction in a mixture containing1.4mol of Al.Results also showed that when x≤1.3,type of reaction becomes gradual,which in turn brings about the incompleteness reaction and residue of initial reagents.
