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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.
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页码:2621 / 2630
页数:10
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