Influence of Ni/SiO2 catalyst preparation methods on hydrogen production from the pyrolysis/reforming of refuse derived fuel

被引:28
作者
Blanco, Paula H. [1 ]
Wu, Chunfei [1 ]
Williams, Paul T. [1 ]
机构
[1] Univ Leeds, Energy Res Inst, Leeds LS2 9JT, W Yorkshire, England
基金
英国工程与自然科学研究理事会;
关键词
Sol-gel; Pyrolysis; Reforming; Gasification; RDF; Nickel catalyst; HIERARCHICAL PORE STRUCTURE; SILICA; ADSORPTION; GASIFICATION; PYROLYSIS; STABILITY; POROSITY; ETHANOL; VOLUME; AREA;
D O I
10.1016/j.ijhydene.2014.01.150
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 from the pyrolysis/reforming of refuse derived fuel (RDF) was investigated with a series of Ni/SiO2 catalysts. The catalysts were prepared by homogeneous precipitation derived from a sol-gel method (HPG) and compared to Ni/SiO2 catalysts prepared by adding a phase separation step to the HPG process (B-HPG). All the catalysts had a NiO loading of 10 wt.%, and three different calcination temperatures (500 degrees C, 700 degrees C and 900 degrees C) were used for each method. The prepared Ni/SiO2 catalysts were analysed to determine their surface area, and porosity characteristics; additionally scanning electron microscopy (SEM-EDX), transmission electron microscopy (TEM), infrared spectroscopy (FTIR), and X-Ray diffraction (XRD) analyses were carried out. The results showed that the catalyst prepared by HPG and calcined at 700 degrees C (HPG700), presented a relatively high surface area (similar to 347 m(2) g(-1)), large pore diameter (12.50 nm), and also resulted in the highest catalytic activity towards H-2 production, attaining similar to 60 vol.% hydrogen. The lowest hydrogen concentration of about 42 vol.% was obtained using the catalysts prepared by the combined HPG-phase separation method, and calcined at 900 degrees C (B-HPG900). It was also observed that at calcination temperatures higher than 700 degrees C the catalytic activity for hydrogen production was diminished for both preparation methods. Copyright (C) 2014, Hydrogen Energy Publications, LLC. Published by Elsevier Ltd. All rights reserved.
引用
收藏
页码:5723 / 5732
页数:10
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