Hydrogen production via catalytic steam reforming of the aqueous fraction of bio-oil using nickel-based coprecipitated catalysts

被引:63
|
作者
Bimbela, F. [1 ]
Oliva, M. [1 ]
Ruiz, J. [1 ]
Garcia, L. [1 ]
Arauzo, J. [1 ]
机构
[1] Univ Zaragoza, Aragon Inst Engn Res I3A, Thermochem Proc Grp GPT, ES-50018 Zaragoza, Spain
关键词
Hydrogen; Bio-oil; Steam reforming; Nickel; Coprecipitated catalyst; ACETIC-ACID; FAST PYROLYSIS; MODEL-COMPOUND; BIOMASS; LIQUIDS; REACTOR; PHASE; FUEL;
D O I
10.1016/j.ijhydene.2013.09.038
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
Hydrogen production was studied in the catalytic steam reforming of a synthetic and a real aqueous fraction of bio-oil. Ni/Al coprecipitated catalysts with varying nickel content (23, 28 and 33 relative atomic %) were prepared by an increasing pH technique and tested during 2 h under different experimental conditions in a small bench scale fixed bed setup. The 28% Ni catalyst yielded a more stable performance over time (steam-to-carbon molar ratio, S/C = 5.58) at 650 degrees C and a catalyst weight/organic flow rate (W/m(org)) ratio of 1.7 g catalyst min/g organic. Using the synthetic aqueous fraction as feed, almost complete overall carbon conversion to gas and hydrogen yields close to equilibrium could be obtained with the 28% Ni catalyst throughout. Up to 63% of overall carbon conversion to gas and an overall hydrogen yield of 0.09 g/g organic could be achieved when using the real aqueous fraction of bio-oil, but the catalyst performance showed a decay with time after 20 min of reaction due to severe coke deposition. Increasing the W/m(org) ratio up to 5 g catalyst min/g organic yielded a more stable catalyst performance throughout, but overall carbon conversion to gas did not surpass 83% and the overall hydrogen yield was only ca. 77% of the thermodynamic equilibrium. Increasing reaction temperatures (600-800 degrees C) up to 750 degrees C enhanced the overall carbon conversion to gas and the overall yield to hydrogen. However, at 800 degrees C the catalyst performance was slightly worse, as a result of an increase in thermal cracking reactions leading to an increased formation of carbon deposits. Copyright (C) 2013, Hydrogen Energy Publications, LLC. Published by Elsevier Ltd. All rights reserved.
引用
收藏
页码:14476 / 14487
页数:12
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