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作 者:陈明树[1] 翁维正[1] 万惠霖[1] 许翩翩[1]
机构地区:[1]厦门大学化学系物理化学研究所固体表面物理化学国家重点实验室
出 处:《厦门大学学报(自然科学版)》1999年第4期556-561,共6页Journal of Xiamen University:Natural Science
基 金:国家科技部攀登预选项目;教育部高等学校博士学科点专项科研基金
摘 要:用XRD、Raman、FT-IR、51V-NMR、Py-IR和TPR-TPO表征SiO2或SiO2上预负载MgO后负载的钒氧化物催化剂体系.SiO2上直接负载钒氧化物,在钒负载量约为5wt%V2O5时出现V2O5晶相,而预负载MgO的在相同钒含量时则没有出现V2O5晶相,表明预负载MgO促进了钒氧化物在载体表面的分散.预负载MgO的催化剂的可还原性和其还原态活化气相氧的活性较低,有较好的丙烷氧化脱氢的丙烯选择性,同时又因有较强的表面酸性位,有利于对丙烷仲碳C-H键的活化,而能保持其较高的丙烷氧化脱氢活性.钒氧物种与载体形成V-O-Mg(Si)桥键。The SiO 2 and MgO/SiO 2 supported vanadia base catalysts were characterized by XRD, Raman, FT IR, 51 V NMR, Py IR and TPR TPO. The results showed that the vanadia were highly dispersed on the MgO pre supported V 2O 5/MgO/SiO 2 catalysts, while vanadia phase was detected in the direct supported V 2O 5/SiO 2 catalysts. The reducibility and reoxidability of the V 2O 5/MgO/SiO 2 catalysts are weaker than that of V 2O 5/SiO 2 catalysts, thus displaying higher propene selectivity. In the other hand, the surface acid sites of V 2O 5/MgO/SiO 2 catalysts were more and stronger, which are favorable to activating the second (2°) C H bond in propane molecular, and thus increasing the activity of propane oxidehydrogenation. The bridge oxygen species (V O Mg/or Si) might be the active oxygen species for propane oxidehydrogenation.
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