首页> 外文会议>Third Tokyo Conference on Advanced Catalytic Science and Technology,Tokyo July 19-24,1998 >Influence of alumina dissolution on the final state of MoO_x/Al_2O_3 catalysts
【24h】

Influence of alumina dissolution on the final state of MoO_x/Al_2O_3 catalysts

机译:氧化铝溶解对MoO_x / Al_2O_3催化剂最终状态的影响

获取原文
获取原文并翻译 | 示例

摘要

This study shows that alumina dissolution controls the speciation of molybdic species deposited on the alumina surface during MoO_x/Al_2O_3 catalysts preparation by the Incipient Wetness method.One hour after the start of the aqueous impregnation step we can easily identify the formation of bulk (NH_4)_3[Al(OH)_6Mo_6O_18] with XRD.This is a clear evidence that there is an extensive reaction of molybdate ions with dissolved aluminum atoms during the preparation procedure.This phenomenon was previously demonstrated in the preparation of MoO_x/Al_2O_3 catalysts by the Equilibrium Adsorption method,and we show here that this occurs also during Incipient Wetness impregnation.In this latter case,the aluminomolybic species deposited on the support is not dispersed at the molecular level but precipitates as a bulk species.The formation of this spedcies can be avoided by a fast impregnation step followed by freezing the solid in liquid nitrogen and drying it under vacuum (freeze-drying).We also show that the nature of the catalyst obtained after calcination at 400 deg C is dependent on the nature of the molybdic speciesobtained after the initial queous impregnation step.For the catalysts obtained by the classical Incipient Wetness impregnation,we can identify bulk MoO_3 by XRD for loadings as low as 7 Mo wt
机译:这项研究表明,通过初湿法制备MoO_x / Al_2O_3催化剂过程中,氧化铝的溶解控制着沉积在氧化铝表面的钼物种的形态。在水浸渍步骤开始一小时后,我们可以轻松地识别出块状(NH_4) _3 [Al(OH)_6Mo_6O_18]的XRD。这清楚地证明了在制备过程中钼酸根离子与溶解的铝原子发生了广泛的反应。这种现象先前已在平衡法制备MoO_x / Al_2O_3催化剂中得到了证明。吸附法,我们在这里表明这也发生在初期润湿浸渍中。在后一种情况下,沉积在载体上的铝钼物质不是在分子水平上分散而是作为大块物质沉淀。可以避免这种现象的形成。通过快速浸渍步骤,然后将固体在液氮中冷冻并在真空下干燥(冷冻干燥)。 o表明在400摄氏度下煅烧后获得的催化剂的性质取决于初始水性浸渍步骤后获得的钼物种的性质。对于经典的初湿法浸渍获得的催化剂,我们可以通过XRD鉴定出MoO_3的体积负载低至7 Mo wt

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