Methane autothermal reforming with CO2 and O2 to synthesis gas at the boundary between Ni and ZrO2

被引:42
|
作者
Gao, Jing [1 ]
Hou, Zhaoyin [1 ]
Liu, Xuesong [2 ]
Zeng, Yaowu [3 ]
Luo, Mengfei [2 ]
Zheng, Xiaoming [1 ]
机构
[1] Zhejiang Univ, Dept Chem, Key Lab Appl Chem Zhejiang Prov, Hangzhou 310028, Zhejiang, Peoples R China
[2] Zhejiang Normal Univ, Inst Phys Chem, Zhejiang Key Lab React Chem Solid Surfaces, Jinhua 321004, Peoples R China
[3] Zhejiang Univ, Ctr Anal & Measurement, Hangzhou 310028, Zhejiang, Peoples R China
基金
中国国家自然科学基金;
关键词
Ni-ZrO2; boundary; CO2; Methane; Activation; Autothermal reforming; FLUIDIZED-BED REACTOR; PARTIAL OXIDATION; SYNGAS PRODUCTION; NANOCOMPOSITE NI/ZRO2; CATALYTIC CONVERSION; FIXED-BED; NI/SIO2; TEMPERATURE; PRECURSORS; SUPPORT;
D O I
10.1016/j.ijhydene.2009.02.074
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
A series of different amount ZrO2-promoted SiO2 supported Ni catalysts were prepared and used for methane autothermal reforming with CO2 and O-2 [MATR] to synthesis gas in a fluidized bed reactor. Pulse-injected surface reactions and in situ XRD characterizations disclosed that CO2 dissociated exclusively at the boundary between Ni and ZrO2. O species derived from CO2 dissociation overflowed to metallic Ni and accelerated the activation of methane. Ni/5ZrO(2)-SiO2 catalyst with larger Ni-ZrO2 boundary exhibited the best activity and stability for MATR even at an extremely space velocity 90,000 h(-1). (C) 2009 International Association for Hydrogen Energy. Published by Elsevier Ltd. All rights reserved.
引用
收藏
页码:3734 / 3742
页数:9
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