A series of CuO-ZnO-Al2O3/HZSM-5 nanocatalysts prepared by impregnation, co-precipitation-physically mixing and combined co-precipitation-ultrasound methods and their catalytic activity investigated toward direct conversion of syngas to DME. BET, XRD, FESEM, TPR-H-2 and FTIR techniques were used to characterize nanocatalysts. XRD and FTIR results showed that structure of HZSM-5 is not damaged even after it is loaded with CuO-ZnO-Al2O3 nanoparticles. TPR-H-2 profiles indicated that reducibility of co-precipitation-ultrasound nanocatalyst is higher than other catalysts. It is found that employing ultrasound energy has great influence on the dispersion of nanocatalyst and its catalytic performance. Size distribution histogram of this nanocatalyst indicated that active phase particle size is between 25.7 and 125.4 nm and their average size is 47.86 nm. The physically mixing of CuO-ZnO-Al2O3 and HZSM-5 resulted in the low catalytic activity, indicating that the closest packing of both active sites for CO hydrogenation and methanol dehydration is necessary for direct synthesis of DME. The nanocatalyst loses negligible activity over the course of reaction due to coke formation on copper species. (C) 2012 The Institution of Chemical Engineers. Published by Elsevier B.V. All rights reserved.
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Pontificia Univ Catolica Rio Janeiro, Dept Quim, PUC Rio, Rua Marques de Sao Vicente 225, BR-22453900 Rio De Janeiro, RJ, BrazilPontificia Univ Catolica Rio Janeiro, Dept Quim, PUC Rio, Rua Marques de Sao Vicente 225, BR-22453900 Rio De Janeiro, RJ, Brazil
Flores, Jhonny Huertas
Pais da Silva, Maria Isabel
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Pontificia Univ Catolica Rio Janeiro, Dept Quim, PUC Rio, Rua Marques de Sao Vicente 225, BR-22453900 Rio De Janeiro, RJ, BrazilPontificia Univ Catolica Rio Janeiro, Dept Quim, PUC Rio, Rua Marques de Sao Vicente 225, BR-22453900 Rio De Janeiro, RJ, Brazil