Deactivation Kinetics of a HZSM-5 Zeolite Catalyst Treated with Alkali for the Transformation of Bio-Ethanol into Hydrocarbons

被引:34
作者
Gayubo, Ana G. [1 ]
Alonso, Ainhoa [1 ]
Valle, Beatriz [1 ]
Aguayo, Andres T. [1 ]
Bilbao, Javier [1 ]
机构
[1] Univ Basque Country, Dept Ingn Quim, E-48080 Bilbao, Spain
关键词
biorefinery; bioethanol; olefins; HZSM-5; zeolite; deactivation; kinetic model; AQUEOUS-ETHANOL; METHANOL; CONVERSION; BIOETHANOL; COKE; H-ZSM-5; OLEFINS; FUEL; ACIDITY; ETHYLENE;
D O I
10.1002/aic.12600
中图分类号
TQ [化学工业];
学科分类号
081705 [工业催化];
摘要
The kinetics of deactivation by coke of a HZSM-5 zeolite catalyst in the transformation of bioethanol into hydrocarbons has been studied. To attenuate deactivation, the following treatments have been carried out: (i) the zeolite has been subjected to a treatment with alkali to reduce the acid strength of the sites and (ii) it has subsequently been agglomerated into a macro and meso-porous matrix of bentonite and alumina. The experimental study has been conducted in a fixed bed reactor under the following conditions: temperature, between 300 and 400 degrees C; pressure, 1 atm; space-time, up to 1.53 (g of catalyst) h (g of ethanol)(-1); particle size of the catalyst, between 0.3 and 0.6 mm; feed flowrate, 0.16 cm(3) min(-1) of ethanol+water and 30 cm(3) (NC) min(-1) of N-2; water content in the feed, up to 75 wt %; time on stream, up to 31 h. The expression for deactivation kinetics is dependent on the concentration of hydrocarbons and water in the reaction medium (which attenuates the deactivation) and, together with the kinetics at zero time on stream, allows the calculation of the evolution with time on stream of the yields and distribution of products (ethylene, propylene and butenes, C-1-C-3 paraffins, and C-4-C-12). By increasing the temperature in the 300-400 degrees C range the role of ethylene on coke deposition is more significant than that of the other hydrocarbons (propylene, butenes and C-4-C-12), which contribute to a greater extent to the formation of coke at 300 degrees C. (C) 2011 American Institute of Chemical Engineers AIChE J, 58: 526-537, 2012
引用
收藏
页码:526 / 537
页数:12
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