首页> 外文期刊>Journal of Catalysis >Application of the unique redox properties of magnesium ortho-vanadate incorporated with palladium in the unsteady-state operation of the oxidative dehydrogenation of propane
【24h】

Application of the unique redox properties of magnesium ortho-vanadate incorporated with palladium in the unsteady-state operation of the oxidative dehydrogenation of propane

机译:钯结合的原钒酸镁独特的氧化还原特性在丙烷氧化脱氢的非稳态操作中的应用

获取原文
获取原文并翻译 | 示例
           

摘要

The oxidative dehydrogenation of propane on Pd2+-incorporated magnesium ortho-vanadate (Pd-ortho-MgVO) was examined, despite the long-held belief that magnesium ortho-vanadate (Mg3V2O8) demonstrates scant catalytic activity in oxidative dehydrogenation. At 0.75 h on-stream, a higher activity than that on magnesium pyro-vanadate (monoclinic Mg2V2O7), which is believed to be one of the more active catalysts for oxidative dehydrogenation, was observed using 5% Pd-ortho-MgVO. Unfortunately, the higher catalytic activity decreased with time on stream due to the rapid abstraction of lattice oxygen from 5% Pd-ortho-MgVO. Although the abstracted lattice oxygen was not regenerated during oxidative dehydrogenation in the presence of excess gaseous oxygen, it was easily regenerated during reoxidation in the absence of propane in the feedstream. Redox cycles of palladium and vanadium species during the catalytic reaction and reoxidation were confirmed using extended X-ray absorption fine structure around the Pd K-edge and V-51 magic-angle spinning nuclear magnetic resonance, respectively. The results of the present study suggest that the higher catalytic activity observed using 5% Pd-ortho-MgVO at 0.75 h on-stream can be maintained by using an unsteady-state operation in combination with the catalytic reaction and catalyst reoxidation. (C) 2008 Elsevier Inc. All rights reserved.
机译:尽管长期以来人们一直认为原钒酸镁(Mg3V2O8)在氧化脱氢中显示出很少的催化活性,但仍研究了丙烷在Pd2 +结合的原钒酸镁(Pd-原-MgVO)上的氧化脱氢作用。在运行0.75 h时,使用5%Pd-邻位MgVO可以观察到比焦钒酸镁(单斜晶Mg2V2O7)活性更高的活性,后者被认为是氧化脱氢活性更高的催化剂之一。不幸的是,由于从5%的Pd-邻位-MgVO中快速夺取了晶格氧,因此较高的催化活性随生产时间的延长而降低。尽管在过量气态氧存在下在氧化脱氢过程中提取的晶格氧并没有再生,但在进料流中没有丙烷的情况下,其在再氧化过程中很容易再生。分别在Pd K边缘和V-51幻角旋转核磁共振周围使用扩展的X射线吸收精细结构,证实了催化反应和再氧化过程中钯和钒物种的氧化还原循环。本研究的结果表明,通过使用非稳态操作与催化反应和催化剂再氧化相结合,可以在0.75 h的运行中使用5%Pd-邻-MgVO观察到更高的催化活性。 (C)2008 Elsevier Inc.保留所有权利。

著录项

相似文献

  • 外文文献
  • 中文文献
  • 专利
获取原文

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号