Methanol steam reforming in an Al2O3 supported thin Pd-layer membrane reactor over Cu/ZnO/Al2O3 catalyst

被引:48
作者
Liguori, S. [1 ]
Iulianelli, A. [1 ]
Dalena, F. [2 ]
Piemonte, V. [3 ]
Huang, Y. [4 ]
Basile, A. [1 ]
机构
[1] Univ Calabria, Italian Natl Res Council, CNR ITM, Inst Membrane Technol, I-87036 Arcavacata Di Rende, CS, Italy
[2] Univ Calabria, Dept Chem & Chem Technol, I-87036 Arcavacata Di Rende, CS, Italy
[3] Univ Campus Biomed Rome, I-00148 Rome, Italy
[4] Nanjing Univ Technol, Coll Chem & Chem Engn, State Key Lab Mat Oriented Chem Engn, Nanjing 210009, Jiangsu, Peoples R China
关键词
High-grade hydrogen production; Methanol steam reforming; Supported Pd/Al2O3 membrane; HYDROGEN-PRODUCTION; FUEL PROCESSOR; H-2; PRODUCTION; GENERATION; PALLADIUM; PURIFICATION; HYDROCARBONS; SEPARATION; COCURRENT; GAS;
D O I
10.1016/j.ijhydene.2013.11.113
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
In this experimental study, a membrane reactor housing a composite membrane constituted by a thin Pd-layer supported onto Al2O3 is utilized to perform methanol steam reforming reaction to produce high-grade hydrogen for PEM fuel cell applications. The influence of various parameters such as temperature, from 280 to 330 degrees C, and pressure, from 1.5 to 2.5 bar, is analyzed. A commercial Cu/Zn-based catalyst is packed in the annulus of the membrane reactor and the experimental tests are performed at space velocity equal to 18,500 h(-1) and H2O:CH3OH feed molar ratio equal to 2.5:1. Results in terms of methanol conversion, hydrogen recovery, hydrogen yield and products selectivities are given. As a best result of this work, 85% of methanol conversion and a highly pure hydrogen stream permeated through the membrane with a CO content lower than 10 ppm were reached at 330 degrees C and 2.5 bar. Furthermore, a comparison between the experimental results obtained in this work and literature data is proposed and discussed. Copyright (C) 2013, Hydrogen Energy Publications, LLC. Published by Elsevier Ltd. All rights reserved.
引用
收藏
页码:18702 / 18710
页数:9
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