Improved hydrogen production from dry reforming reaction using a catalytic packed-bed membrane reactor with Ni-based catalyst and dense PdAgCu alloy membrane

被引:55
作者
Sumrunronnasak, Sarocha [1 ]
Tantayanon, Supawan [2 ]
Kiatgamolchai, Somchai [3 ]
Sukonket, Thitinat [4 ]
机构
[1] Chulalongkorn Univ, Fac Sci, Grad Program Petrochem & Polymer Sci, Bangkok 10330, Thailand
[2] Chulalongkorn Univ, Dept Chem, Fac Sci, Green Chem Res Lab, Bangkok 10330, Thailand
[3] Chulalongkorn Univ, Dept Phys, Fac Sci, Bangkok 10330, Thailand
[4] Suan Dusit Rajabhat Univ, Fac Sci & Technol, Occupat Hlth & Safety Sci Program, 295 Nakhon Ratchasima Rd, Bangkok 10300, Thailand
关键词
PdAgCu alloy membrane; Hydrogen production; Dry reforming; Catalytic membrane reactor; Ni-based catalyst; PD-BASED MEMBRANE; WATER-GAS SHIFT; PALLADIUM MEMBRANES; H-2; PRODUCTION; METHANE; SEPARATION; PERFORMANCE; PERMEATION; BINARY; SYNGAS;
D O I
10.1016/j.ijhydene.2015.10.129
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
A catalytic Pd76Ag19Cu5 alloy membrane reactor packed with 5% Ni/Ce0.6Zr0.4O2 catalyst was adopted in this study to investigate hydrogen production performance from the dry reforming reaction of methane and carbon dioxide. The 1:1 CH4/CO2 feed was introduced to the reactor with 60 mg of the catalyst at a flow rate of 20 ml/min at 550 degrees C. The effluent gas compositions were examined using an online gas chromatographer (GC). Compared to a conventional reactor without the membrane, the CH4 and CO2 conversions were significantly increased by 3.5-fold and 1.5-fold, respectively. Correspondingly, the overall H-2 yield was greatly improved from about 10-35%. Additionally, the hydrogen selectivity increased from 47 to 53%. It is theorized that the in-situ partial hydrogen withdrawal by the membrane mainly caused the dry reforming reaction equilibrium to shift forward and created a hydrogen-deprived environment unfavorable for the competing reversible water-gas shift reaction to take place. Copyright (C) 2015, Hydrogen Energy Publications, LLC. Published by Elsevier Ltd. All rights reserved.
引用
收藏
页码:2621 / 2630
页数:10
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