Ni/Y2O3-ZrO2 catalyst for hydrogen production through the glycerol steam reforming reaction

被引:105
作者
Charisiou, N. D. [1 ]
Siakavelas, G. [1 ]
Tzounis, L. [2 ]
Dou, B. [3 ]
Sebastian, V. [4 ,5 ]
Hinder, S. J. [6 ]
Baker, M. A. [6 ]
Polychronopoulou, K. [7 ,8 ]
Goula, M. A. [1 ]
机构
[1] Western Macedonia Univ Appl Sci, Dept Environm & Pollut Control Engn, Lab Alternat Fuels & Environm Catalysis, GR-50100 Koila, Kozani, Greece
[2] Univ Ioannina, Dept Mat Sci & Engn, CSML, GR-45110 Ioannina, Greece
[3] Univ Shanghai Sci & Technol, Sch Energy & Power Engn, Shanghai 200093, Peoples R China
[4] Univ Zaragoza, CSIC, ICMA, INA,Chem & Environm Engn Dept, Zaragoza 50018, Spain
[5] CIBERBBN, Networking Res Ctr Bioengn Biomat & Nanomed, Madrid 28029, Spain
[6] Univ Surrey, Fac Engn & Phys Sci, Surface Anal Lab, Guildford GU2 4DL, Surrey, England
[7] Khalifa Univ Sci & Technol, Dept Mech Engn, POB 127788, Abu Dhabi, U Arab Emirates
[8] Khalifa Univ Sci & Technol, Ctr Catalysis & Separat, POB 127788, Abu Dhabi, U Arab Emirates
关键词
Hydrogen production; Glycerol steam reforming; Yttria-stabilised zirconia; Nickel catalysts; Carbon deposition; Deactivation; SYNTHESIS GAS-PRODUCTION; ALUMINA CATALYSTS; SUPPORT COMPOSITION; SYNGAS PRODUCTION; H-2; PRODUCTION; NI CATALYSTS; NICKEL; ZIRCONIA; ETHANOL; ZRO2;
D O I
10.1016/j.ijhydene.2019.04.237
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
In the study presented herein, the catalytic activity and stability of a Ni catalyst supported on Y2O3-ZrO2 was examined for the first time in the glycerol steam reforming reaction and compared with a Ni/ZrO2. The addition of Y2O3 stabilized the ZrO2 tetragonal phase, increased the O-2 storage capacity of the support and the medium strength acid sites of the catalyst, and although the Ni/Zr catalyst had a higher concentration of basic sites, the Ni/YZr presented more stable monodentate carbonates. Moreover, the Ni/YZr had substantially higher Ni surface concentration and smaller Ni particles. These properties influence the gaseous products' distribution by increasing the H-2 yield and selectivity and preventing the transformation of CO2 to CO, by inhibiting the reverse water gas shift (RWGS) reaction from taking place. For both catalysts the main liquid products identified were allyl alcohol, acetaldehyde, acetone, acrolein, acetic acid and acetol; these were subsequently quantified. The time-on-stream experiments showed that the Ni/YZr was more stable during reaction and had a higher H-2 yield after 20 h (2.17 in comparison to 1.50 mol H-2/mol C3H8O3, for the Ni/Zr). Extensive investigation of the carbon deposits showed that although lower amounts of coke were deposited on the Ni/Zr catalyst, these structures were more graphitic in nature and had fewer defects, which means they were harder to oxidize. Moreover, transmission electron microscopy (TEM) analysis showed that sintering of Ni nanoparticles during the reaction was significant for the Ni/Zr catalyst, as the mean particle diameter increased from an initial value of 48.2 to 67.9 nm, while it was almost absent on the Ni/YZr catalyst (the mean particle diameter increased from 42.1 to 47.4 nm). (C) 2019 Hydrogen Energy Publications LLC. Published by Elsevier Ltd. All rights reserved.
引用
收藏
页码:10442 / 10460
页数:19
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