Hydrogen production by steam reforming of acetic acid using hydrotalcite type precursors

被引:18
|
作者
Borges, R. P. [1 ]
Ferreira, R. A. R. [1 ]
Rabelo-Neto, R. C. [2 ]
Noronha, F. B. [2 ]
Hori, C. E. [1 ]
机构
[1] Univ Fed Uberlandia, Sch Chem Engn, Av Joao Naves de Avila 2121,Bloco 1 K, BR-38408144 Uberlandia, MG, Brazil
[2] Natl Inst Technol, Div Catalysis & Chem Proc, Av Venezuela 82, BR-20081312 Rio De Janeiro, RJ, Brazil
关键词
Hydrotalcite; Acetic acid; Aqueous fraction of bio-oil; Hydrogen; FLUIDIZED-BED REACTOR; BIO-OIL PRODUCTION; THERMODYNAMIC ANALYSIS; CATALYST PRECURSORS; PARTIAL OXIDATION; NICKEL-CATALYSTS; MODEL-COMPOUND; AL CATALYSTS; PYROLYSIS; ETHANOL;
D O I
10.1016/j.ijhydene.2018.03.028
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
Acetic acid can be used as a model compound in the study of the steam reforming of the hydrophilic phase of bio-oil. In order to perform acetic acid reforming reactions, low cost catalysts with high catalytic activity and selectivity are required. Thus, Ni-Mg-Al hydro-talcite derived catalysts emerge as a good alternative. In this work, four Ni-Mg-Al hydrotalcite type precursors were prepared, with different Ni/Mg molar ratios (0.3, 0.4, 0.5, and 0.6). Various characterization tests have been performed for the prepared hydrotalcite type precursors. The stability of the catalytic activity was evaluated during 24 h and the used samples were submitted to a thermogravimetric analysis to evaluate carbon accumulation. Characterization tests proved that Ni/Mg ratios had a direct influence in the reducibility of the precursors. The Temperature-programmed surface reaction analysis showed that the steam reforming of acetic acid occurred majorly when the temperature reached 873 K. Stability test showed that precursors 04NiMg and 05NiMg had the best catalytic performance. It was also seen that sample 06NiMg suffered from deactivation by carbon deposition, which was confirmed by the thermogravimetric analysis. (C) 2018 Hydrogen Energy Publications LLC. Published by Elsevier Ltd. All rights reserved.
引用
收藏
页码:7881 / 7892
页数:12
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