Effect of metal amount on the catalytic performance of Ni-Al2O3 catalyst for the Tri-reforming of methane

被引:17
|
作者
Gupta, Satyam [1 ]
Deo, Goutam [1 ,2 ]
机构
[1] Indian Inst Technol Kanpur, Dept Chem Engn, Kanpur 208016, Uttar Pradesh, India
[2] Indian Inst Technol Kanpur, Dept Sustainable Energy Engn, Kanpur 208016, Uttar Pradesh, India
关键词
Tri-reforming of methane; Nickel loading; Reduction temperature; Synthesis gas CO2 conversion; MESOPOROUS NANOCRYSTALLINE ZIRCONIA; SYNTHESIS GAS-PRODUCTION; NICKEL-CATALYSTS; PARTIAL OXIDATION; NI CATALYSTS; PD/SIO2; CATALYSTS; NIAL2O4; FORMATION; SYNGAS PRODUCTION; CARBON-DIOXIDE; HYDROGEN;
D O I
10.1016/j.ijhydene.2022.11.049
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
Mesoporous Ni-Al2O3 catalysts with Ni weight (%) 5 to 15 were synthesized, characterized, and tested for tri-reforming of methane (TRM). The characterization results reveal that the metal loading influences the metal-support interaction of the catalysts. Furthermore, the choice of reduction temperature affected the dispersion of metallic-Ni. It is advantageous to reduce these catalysts at their respective Tmax temperatures, which are obtained from H2-TPR studies. At these conditions, the dispersion was maximum. For TRM at 600 degrees C, the conversions and yields increased with an increase in Ni loading, and carbon was not detected. Increasing the metal loading from 5 wt% to 15 wt% increased the CH4 conversion from 70.5 to 82.4% and CO2 conversion from 10.2 to 19.7%. In contrast, the H2/CO ratio decreased from 3.8 to 3.2. The conversions and yields during TRM were relatively constant with time-on-stream and were highest for 15Ni-Al. Furthermore, H2/CO ratio was >3, and minimal change in dispersion was observed post-reaction for this catalyst. Thus, the active metal loading and the reduction temperature required are important parameters that need to be considered while designing a suitable catalyst for TRM.(c) 2022 Hydrogen Energy Publications LLC. Published by Elsevier Ltd. All rights reserved.
引用
收藏
页码:5478 / 5492
页数:15
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