Yttrium promoted Ni-based double-layered hydroxides for dry methane reforming

被引:83
|
作者
Swirk Da Costa, Katarzyna [1 ,2 ]
Galvez, Maria Elena [1 ]
Motak, Monika [2 ]
Grzybek, Teresa [1 ]
Ronning, Magnus [3 ]
Da Costa, Patrick [1 ]
机构
[1] Sorbonne Univ, CNRS, Inst Jean Le Rond dAlembert, 2 Pl Gare Ceinture, F-78210 St Cyr Lecole, France
[2] AGH Univ Sci & Technol, Fac Energy & Fuels, Adama Mickiewicza Ave 30, PL-30059 Krakow, Poland
[3] Norwegian Univ Sci & Technol, Dept Chem Engn, Sem Saelandsvei 4, N-7491 Trondheim, Norway
关键词
Dry reforming of methane; Carbon dioxide; Nickel; Yttrium; Double-layered hydroxides; MG-AL HYDROTALCITES; CARBON-DIOXIDE; THERMODYNAMIC ANALYSIS; BIMETALLIC CATALYSTS; SUPPORT COMPOSITION; SYNGAS PRODUCTION; TRANSITION-METAL; LOW-TEMPERATURE; SOLID-SOLUTION; CO2;
D O I
10.1016/j.jcou.2018.08.004
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Yttrium modified Ni-based double-layered hydroxides were tested as novel catalysts in dry methane reforming. The catalysts were characterized by XRF, BET analysis, XRD, TPR-H-2, TPD-CO2, TGA/DSC-MS, H-2 chemisorption and TEM. Co-precipitation with yttrium (III) nitrate hexahydrate resulted in increased specific surface area, smaller Ni crystallite size, enhanced reducibility, and higher distribution of weak and medium basic sites as compared to Y-free material. The DRM catalytic tests, carried out in the temperature range of 850-600 degrees C, led to a significant improvement of activity, with the 1.5 wt Y-promoted catalyst being the most efficient in converting both CH4 and CO2. Moreover, the 10 h test at 700 degrees C further confirmed enhanced stability for this HTNi-Y1.5 catalyst. Higher CO2 conversion than CH4 conversion and less CO compared to H-2 proves that side reactions are occurring simultaneously.
引用
收藏
页码:247 / 258
页数:12
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