Aiming to improve the reactive adsorption desulfurization（RADS） performances of Ni/Zn O adsorbents,ZnxAly（OH）2（CO3）z·x H2 O precursor is synthesized by coprecipitation of Zn2＋,AlO-2,and CO2-3; the Zn OZn6A...Aiming to improve the reactive adsorption desulfurization（RADS） performances of Ni/Zn O adsorbents,ZnxAly（OH）2（CO3）z·x H2 O precursor is synthesized by coprecipitation of Zn2＋,AlO-2,and CO2-3; the Zn OZn6Al2O9 composite oxides are obtained by the calcination of ZnxAly（OH）2（CO3）z·x H2 O precursor,and the Ni/Zn O-Zn6Al2O9（6.0 wt% Ni O） adsorbents are prepared by wetness impregnation method. The phase,acid strength,acid type and quantity,morphology,and thermal properties were characterized by X-ray diffraction,temperature-programmed desorption of ammonia,pyridine-adsorbed infrared spectrum,high-resolution transmission electron microscopy,and Thermo Gravimetry-Derivative Thermo Gravimetry（TG-DTG）,respectively. The breakthrough sulfur capacities of six adsorbents are between 34.2 and 47.9 mg/gcat. The kinetic studies indicated that the active energy of RADS（49.4 k J/mol） could reach nano-sized Zn O,the particle size of is about 12.0 nm. All the excellent RADS performances can be due to the high SBET. Also,there are some extents of aromatization reactions that occur,which can be contributed to the B？nsted acid rooted in Zn6Al2O9 composite oxide,and the octane number of products can be preserved well.展开更多
The desulfurater(BaAl2O4) was successfully synthesized with BaCO3 and Al(OH)3 powders as raw materials by microwave sintering method.The mass loss of raw materials and the characterization of the outcome were investig...The desulfurater(BaAl2O4) was successfully synthesized with BaCO3 and Al(OH)3 powders as raw materials by microwave sintering method.The mass loss of raw materials and the characterization of the outcome were investigated by means of TG-DSC,XRD and optical microscopy.The reaction mechanism was discussed.The experimental results show that synthesized BaAl2O4 by microwave sintering method is feasible.Compared with conventional sintering method,microwave sintering is a better way to synthesize BaAl2O4 with advantages of low temperature sintering,short time sintering and high synthesis rate.展开更多
The synthesis of polycrystalline aluminum oxynitride （AlON） powders was investigated by the carbothermal reduction and ni- tridation （CRN） of amorphous precursor obtained by wet chemical processing. Co-precipitati...The synthesis of polycrystalline aluminum oxynitride （AlON） powders was investigated by the carbothermal reduction and ni- tridation （CRN） of amorphous precursor obtained by wet chemical processing. Co-precipitation processing was employed to achieve amorphous precursor from AI（NO3）3 solution dispersed by nanosized carbon particles, which was composed of AI（OH）3 and C particles homogeneously. The effects of the content of carbon black, pH value, and calcination temperature on formation of A1ON phase were investigated by means of XRD, SEM and TEM, respectively. It was found that single phase AION powder could be synthesized when the resultant precursors were calcined at 1750℃ for 2 hours under flowing N2. Un- der optimal additional content of C （5.6wt%）, the resultant A1ON powders exhibited the primary particle size of about 1-3 μm with a specific surface area of 3.2 m2/g, which were superior to that of carbothermal reduction of immediate mixture of γ-A1203/C powders.展开更多
文摘Aiming to improve the reactive adsorption desulfurization（RADS） performances of Ni/Zn O adsorbents,ZnxAly（OH）2（CO3）z·x H2 O precursor is synthesized by coprecipitation of Zn2＋,AlO-2,and CO2-3; the Zn OZn6Al2O9 composite oxides are obtained by the calcination of ZnxAly（OH）2（CO3）z·x H2 O precursor,and the Ni/Zn O-Zn6Al2O9（6.0 wt% Ni O） adsorbents are prepared by wetness impregnation method. The phase,acid strength,acid type and quantity,morphology,and thermal properties were characterized by X-ray diffraction,temperature-programmed desorption of ammonia,pyridine-adsorbed infrared spectrum,high-resolution transmission electron microscopy,and Thermo Gravimetry-Derivative Thermo Gravimetry（TG-DTG）,respectively. The breakthrough sulfur capacities of six adsorbents are between 34.2 and 47.9 mg/gcat. The kinetic studies indicated that the active energy of RADS（49.4 k J/mol） could reach nano-sized Zn O,the particle size of is about 12.0 nm. All the excellent RADS performances can be due to the high SBET. Also,there are some extents of aromatization reactions that occur,which can be contributed to the B？nsted acid rooted in Zn6Al2O9 composite oxide,and the octane number of products can be preserved well.
基金Project(50264001) supported by the National Natural Science Foundation of ChinaProject(QKH-J-2008-2009) supported by Guizhou Science and Technology Department, China
文摘The desulfurater(BaAl2O4) was successfully synthesized with BaCO3 and Al(OH)3 powders as raw materials by microwave sintering method.The mass loss of raw materials and the characterization of the outcome were investigated by means of TG-DSC,XRD and optical microscopy.The reaction mechanism was discussed.The experimental results show that synthesized BaAl2O4 by microwave sintering method is feasible.Compared with conventional sintering method,microwave sintering is a better way to synthesize BaAl2O4 with advantages of low temperature sintering,short time sintering and high synthesis rate.
文摘The synthesis of polycrystalline aluminum oxynitride （AlON） powders was investigated by the carbothermal reduction and ni- tridation （CRN） of amorphous precursor obtained by wet chemical processing. Co-precipitation processing was employed to achieve amorphous precursor from AI（NO3）3 solution dispersed by nanosized carbon particles, which was composed of AI（OH）3 and C particles homogeneously. The effects of the content of carbon black, pH value, and calcination temperature on formation of A1ON phase were investigated by means of XRD, SEM and TEM, respectively. It was found that single phase AION powder could be synthesized when the resultant precursors were calcined at 1750℃ for 2 hours under flowing N2. Un- der optimal additional content of C （5.6wt%）, the resultant A1ON powders exhibited the primary particle size of about 1-3 μm with a specific surface area of 3.2 m2/g, which were superior to that of carbothermal reduction of immediate mixture of γ-A1203/C powders.
