Optimization of H2 production with CO2 capture by steam reforming of methane integrated with a chemical-looping combustion system

被引:31
|
作者
Pans, Miguel A. [1 ]
Abad, Alberto [1 ]
de Diego, Luis F. [1 ]
Garcia-Labiano, Francisco [1 ]
Gayan, Pilar [1 ]
Adanez, Juan [1 ]
机构
[1] Inst Carboquim ICB CSIC, Environm & Energy Dept, Zaragoza 50018, Spain
关键词
Hydrogen production; Chemical-looping combustion; CO2; capture; Oxygen carrier; Iron oxide; HYDROGEN-PRODUCTION; OXYGEN CARRIERS; FLUIDIZED-BED;
D O I
10.1016/j.ijhydene.2013.06.114
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
Methane steam reforming (SR) integrated with a chemical-looping combustion (CLC) system is a new process for producing hydrogen from natural gas, allowing carbon dioxide capture with a low energy penalty. In this study, mass and enthalpy balances of an SR-CLC system were carried out to determine the autothermal operating conditions for optimal H-2 production. The evaluation was conducted using iron-based oxygen carriers. Two configurations were analysed, firstly with the reformer tubes inside the fuel reactor and, secondly, with the reformer tubes inside the air reactor. This paper analyses the effect of two parameters affecting the SR process, namely the conversion of methane in the reformer (X-CH4) and the efficiency of the hydrogen separation of a pressure swing adsorption (PSA) unit (eta(PSA)), as well as two parameters affecting the CLC system, namely the Fe2O3 content in the oxygen carrier and its conversion variation (Delta X-OC), on the H-2 yields. Moreover, it also analyses the reduction of Fe2O3 to Fe3O4 or to FeAl2O4. The results shown that a H-2 yield value of 2.45 mol H-2 per mol of CH4 can be obtained with the reformer tubes located inside the air reactor and with Fe2O3 being reduced to Fe3O4. This corresponds to a (CH4) to H-2 conversion of 74.2%, which is similar to state-of-the-art H-2 production technologies, but with inherent CO2 capture in the SR-CLC process. Copyright (C) 2013, Hydrogen Energy Publications, LLC. Published by Elsevier Ltd. All rights reserved.
引用
收藏
页码:11878 / 11892
页数:15
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