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Structure and SO3 decomposition activity of CeVO4/SiO2 catalysts for solar thermochemical water splitting cycles

机译:CeVO4 / SiO2催化剂在太阳热化学分水循环中的结构和SO3分解活性

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摘要

Ce-V oxide catalysts supported on bimodal mesoporous SiO2 were prepared by a wet impregnation method to study their catalytic activity for SO3 decomposition, which is a key step in thermochemical water splitting cycles based on the sulfur iodine process. As-prepared Ce-V/SiO2 catalysts exhibited more than 50-fold higher turnover frequency at 600 degrees C compared to unsupported CeVO4. This is in accordance with the smaller size (13 nm) of CeVO4 particles highly dispersed in SiO2 mesopores, compared to approximately 600 nm for unsupported CeVO4 particles. The Ce-V/SiO2 catalysts exhibited a higher activity than supported V2O5 or CeO2 catalysts, which coexisted depending on the Ce/V ratio. Among the studied catalysts with different Ce/V molar ratios, the highest activity was achieved at Ce/V = 0.9, at which the greatest specific surface area of CeVO4 was attained. The catalyst demonstrated SO3 decomposition rates comparable to those of Pt/Al2O3 in a wide range of WHSV (3.6-110 g-H2SO4 g(-1) h(-1)) and no indication of noticeable deactivation during 40 h of the catalytic reaction at 650 degrees C. Copyright (C) 2015, Hydrogen Energy Publications, LLC. Published by Elsevier Ltd. All rights reserved.
机译:通过湿法浸渍法制备了双峰介孔SiO2负载的Ce-V氧化物催化剂,研究了其对SO3分解的催化活性,这是基于硫碘过程的热化学分水循环的关键步骤。与未负载的CeVO4相比,制备的Ce-V / SiO2催化剂在600摄氏度下的周转频率高出50倍以上。这与高度分散在SiO2中孔中的CeVO4颗粒的尺寸较小(13 nm)有关,相比之下,未负载的CeVO4颗粒约为600 nm。 Ce-V / SiO2催化剂显示出比负载的V2O5或CeO2催化剂更高的活性,后者根据Ce / V比率共存。在所研究的具有不同Ce / V摩尔比的催化剂中,在Ce / V = 0.9时获得了最高的活性,在该处获得了CeVO4的最大比表面积。在宽范围的WHSV(3.6-110 g-H2SO4 g(-1)h(-1))中,该催化剂的SO3分解速率与Pt / Al2O3相当,并且在催化反应40小时内没有明显的失活迹象在650摄氏度下进行。版权所有(C)2015,氢能出版物有限公司。由Elsevier Ltd.出版。保留所有权利。

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