Combined air partial oxidation and CO2 reforming of coal bed methane to synthesis gas over co-precipitated Ni-Mg-ZrO2 catalyst

被引:16
|
作者
Sun, Laizhi [1 ,2 ]
Tan, Yisheng [1 ]
Zhang, Qingde [1 ]
Xie, Hongjuan [1 ]
Han, Yizhuo [1 ]
机构
[1] Chinese Acad Sci, Inst Coal Chem, State Key Lab Coal Convers, Taiyuan 030001, Shanxi, Peoples R China
[2] Chinese Acad Sci, Grad Univ, Beijing 100039, Peoples R China
关键词
Catalytic air partial oxidation; CO2; reforming; Coal bed methane; Synthesis gas; Ni-Mg-ZrO2; catalyst; MGO SOLID-SOLUTION; SUPPORTED NI CATALYSTS; CARBON-DIOXIDE; SYNGAS PRODUCTION; NATURAL-GAS; TEMPERATURE PROFILE; NOBLE-METALS; STEAM; CONVERSION; O-2;
D O I
10.1016/j.ijhydene.2011.07.010
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 present study aims at exploring a concept which can convert coal-bed methane (containing methane, air and carbon dioxide) to synthesis gas. Without pre-separation and purification, the low-cost synthesis gas can be produced by coupling air partial oxidation and CO2 reforming of coal bed methane. For this purpose, the co-precipitated Ni-Mg-ZrO2 catalyst was prepared. It was found that the co-precipitated Ni-Mg-ZrO2 catalyst exhibited the best activity and stability at 800 degrees C during the reaction. The conversions of CH4 and CO2 maintained at 94.8% and 82.1% respectively after 100 h of reaction. The effect of reaction temperature was investigated. The H-2/CO ratio in the product was mainly dependent on the feed gas composition. By changing O-2/CO2 ratio of the feed gases, the H-2/CO ratio in the off-gas varied between 0.8 and 1.8. The experimental results showed that the high thermal stability and basic properties of the catalyst, and the strong metal-support interaction played important roles in improving the activity and stability of the catalyst. With the combined reactions and the Ni-Mg-ZrO2 catalyst, the coal bed methane could be converted to synthesis gas, which can meet the need of the subsequent synthesis processes. Copyright (C) 2011, Hydrogen Energy Publications, LLC. Published by Elsevier Ltd. All rights reserved.
引用
收藏
页码:12259 / 12267
页数:9
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