Hydrogen production through combined dry reforming and partial oxidation of methane over the Ni/Al2O3-CeO2 catalysts

被引:17
作者
Babakouhi, Reza [1 ]
Alavi, Seyed Mehdi [1 ]
Rezaei, Mehran [1 ]
Jokar, Farzad [1 ]
Varbar, Mohammad [1 ]
Akbari, Ehsan [1 ]
机构
[1] Iran Univ Sci & Technol, Catalyst & Nanomat Res Lab CNMRL, Coll Chem Petr & Gas Engn, Tehran, Iran
基金
美国国家科学基金会;
关键词
Combined reforming; Dry reforming; Coke formation; Alumina; Nickel -based catalysts; METAL-SUPPORT INTERACTION; SYNGAS PRODUCTION; NI/MGAL2O4; CATALYSTS; NANOCRYSTALLINE LA; NI-CATALYST; CE; NANOCATALYSTS; ZR; COMBINATION; COMBUSTION;
D O I
10.1016/j.ijhydene.2024.02.220
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
The study aimed to explore synergies resulting from the combination of dry reforming and partial oxidation of methane, using 10%Ni/Al2O3-CeO2 catalysts with varying CeO2 proportions (10, 30, 50, and 70 wt%). The manufacturing involved mechanochemical and impregnation methods for supports and catalysts, respectively. The inclusion of 10 wt% CeO2 played a crucial role in enhancing nickel dispersion and reinforcing interaction with the support. Particularly noteworthy was the exceptional performance of the 10%Ni/Al2O3-10%CeO2 catalyst, achieving an impressive 83% methane conversion at 700 degrees C, surpassing other prepared nickel -based catalysts. The introduction of a small quantity of O2 during methane dry reforming, inferred from TPO and FESEM analyses, effectively mitigated carbon deposition. Demonstrating remarkable endurance, the catalyst 10%Ni/Al2O3-10%CeO2 maintained efficacy for 440 min at 700 degrees C, yielding CH4 and CO2 conversion rates of 93% and 34%, respectively. Higher calcination temperatures led to nickel particle aggregation, causing a decline in catalytic efficiency.
引用
收藏
页码:503 / 514
页数:12
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