Supercritical antisolvent process to produce cerium oxide nanoparticles as a support for high-activity platinum catalysts

被引:0
|
作者
Palma V. [1 ]
Pietrosanto A. [1 ]
Martino M. [1 ]
Reverchon E. [1 ]
De Marco I. [1 ]
机构
[1] University of Salerno, Department of Industrial Engineering, Via Giovanni Paolo II, 132, Fisciano (SA)
来源
De Marco, Iolanda (idemarco@unisa.it) | 1600年 / Italian Association of Chemical Engineering - AIDIC卷 / 57期
关键词
Cerium oxide nanoparticle - Different pressures - Field emission scanning electron microscopy - Mercury porosimetry - Nitrogen adsorption and desorptions - Operating condition - Supercritical antisolvent process - Water gas shift (WGS) reaction;
D O I
10.3303/CET1757162
中图分类号
学科分类号
摘要
Cerium acetylacetonate (Ce(acac)3) was precipitated from methanol (MeOH) using supercritical antisolvent process (SAS). The precursor was, then, calcined obtaining the cerium oxide (CeO2). Platinum (Pt) supported on cerium oxide is active for the water gas shift reaction, showing higher activity if compared with platinum supported on other oxides. The catalyst based on platinum supported on cerium oxide obtained using SAS process is more active than the Pt/CeO2 catalyst obtained in a conventional manner. The precursor nanoparticles were precipitated at different pressures and concentrations of the Ce(acac)3/MeOH solution. At the best operating conditions, nanoparticles with a diameter in the range 40-65 nm were obtained. The catalytic activity and the selectivity of two different samples was studied and compared. The catalysts were characterized by X-ray diffraction, field emission scanning electron microscopy, infrared spectroscopy, nitrogen adsorption and desorption at 77 K, and mercury porosimetry. © Copyright 2017, AIDIC Servizi S.r.l.
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页码:967 / 972
页数:5
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