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Frontiers of Chemical Science and Engineering

ISSN 2095-0179

ISSN 2095-0187(Online)

CN 11-5981/TQ

Postal Subscription Code 80-969

2018 Impact Factor: 2.809

Front Chem Sci Eng    2013, Vol. 7 Issue (3) : 270-278    https://doi.org/10.1007/s11705-013-1337-2
RESEARCH ARTICLE
Sustainable H2 production from ethanol steam reforming over a macro-mesoporous Ni/Mg-Al-O catalytic monolith
Ruixue GU1, Guangming ZENG1, Jingjing SHAO1, Yuan LIU1, Johannes W. Schwank2, Yongdan LI()
1. Tianjin Key Laboratory of Applied Catalysis Science and Technology and State Key Laboratory for Chemical Engineering (Tianjin University), School of Chemical Engineering, Tianjin University, Tianjin 300072, China; 2. Department of Chemical Engineering, University of Michigan, Ann Arbor, MI 48109-2136, USA
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Abstract

A macro-meso-porous monolithic Ni-based catalyst was prepared via an impregnation route using polystyrene foam as the template and then used in the steam reforming of ethanol to produce a H2-rich gas. The Ni/Mg-Al catalyst has a hierarchically macro-meso-porous structure as indicated by photographs and scanning electron microscopy (SEM). The surface area of the catalyst was 230 m2?g-1 and the Ni dispersion was 5.62%. Compared to the pelletized sample that was prepared without a template, the macro-meso-porous Ni/Mg-Al monolith exhibited superior reactivity in terms of H2 production and also had lower CH4 yields at 700oC and 800oC. Furthermore, the monolithic catalyst maintained excellent activity and H2 selectivity after 100-h on-stream at 700oC, as well as good resistance to coking and metal sintering.

Keywords macroporous Ni-based catalyst      monolith      hydrogen production      ethanol steam reforming     
Corresponding Author(s): LI Yongdan,Email:ydli@tju.edu.cn   
Issue Date: 05 September 2013
 Cite this article:   
Ruixue GU,Guangming ZENG,Jingjing SHAO, et al. Sustainable H2 production from ethanol steam reforming over a macro-mesoporous Ni/Mg-Al-O catalytic monolith[J]. Front Chem Sci Eng, 2013, 7(3): 270-278.
 URL:  
https://academic.hep.com.cn/fcse/EN/10.1007/s11705-013-1337-2
https://academic.hep.com.cn/fcse/EN/Y2013/V7/I3/270
Fig.1  Photographs of the monoliths (a) PS template, (b) AlO, (c) MgO-AlO, (d) sample 1
Fig.2  SEM images of PS template. Scale bars: 200 mm for (a) and 20 mm for (b)
Fig.3  SEM images of monolith materials (a) AlO, (b) MgO-AlO, (c) sample 1
Fig.4  XRD patterns of the monolithic AlO and MgO-AlO supports and sample 1 and sample 2 before reduction
SampleChemical composition /(wt-%)BET surface area /(m2?g-1)Average pore diameter /nmPore volume /(cm3?g-1)Ni dispersion /%Surface area of Ni /(m2?gcat-1)
NiMgAl
PS---2858.640.464--
Al2O3a)--52.72618.190.433--
MgO-Al2O3a)-16.938.32357.320.400--
Sample 19.8615.835.22307.640.3935.6237.0
Sample 210.115.535.11144.820.2512.4816.7
Tab.1  Chemical composition, BET surface area, average pore size, pore volume, Ni dispersion and Ni surface area of the different materials
Fig.5  TPR profiles of the catalysts of sample 1 and sample 2
SampleH2CO2CH4COC2H4
1-700a)4.710.5000.0461.46-
1-8004.830.5100.0231.47-
2-7004.050.7000.3500.9390.011
2-8004.520.5630.0901.35-
Tab.2  The product distribution after 21 h time-on-stream /mol·mol ethanol for different samples
Fig.6  CH yields during the ESR reaction at 700°C and 800°C as a function of time (1–, = reaction temperature)
SampleRelative coke formation /wt-%
1-700 a)11.25
1-8008.54
2-70039.66
2-80035.54
Tab.3  Relative coke accumulated on sample 1 and sample 2 after reaction at different temperatures for 21 h
Fig.7  Stability test of the (a) sample 1 and (b) sample 2 ( = 700°C, HO/CHOH= 3, time= 100 h, flow rate of mixed solution= 4 mL?h)
Fig.8  TEM images of the used catalyst after reaction at 700°C for 100 h: (a) sample 1; (b) sample 2
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