Temperature-dependent anti-coking behaviors of highly stable Ni-CaO-ZrO2 nanocomposite catalysts for CO2 reforming of methane

被引:60
|
作者
Chen, Qingjun [1 ]
Zhang, Jun [1 ]
Pan, Bingrong [1 ]
Kong, Wenbo [1 ]
Chen, Yuyun [1 ]
Zhang, Weili [1 ]
Sun, Yuhan [1 ,2 ]
机构
[1] Chinese Acad Sci, Shanghai Adv Res Inst, CAS Key Lab Low Carbon Convers, Ctr Sci & Engn, Shanghai 201210, Peoples R China
[2] Chinese Acad Sci, Inst Coal Chem, State Key Lab Coal Convers, Taiyuan 030001, Shanxi, Peoples R China
基金
中国国家自然科学基金;
关键词
Coking; Nickel-based catalysts; CO2 reforming of methane; Strong metal-support interaction (SMSI); SYNTHESIS GAS; THERMODYNAMIC ANALYSIS; BIMETALLIC CATALYSTS; NICKEL-CATALYST; SUPPORT; METAL; CH4; PARAMETERS; CEO2; MGO;
D O I
10.1016/j.cej.2017.03.029
中图分类号
X [环境科学、安全科学];
学科分类号
08 ; 0830 ;
摘要
Coking is one of the main obstacles to the application of Ni-based catalysts for CO2 (dry) reforming of methane (DRM). In this work, the anti-coking behaviors of a highly stable Ni-CaO-ZrO2 nanocomposite catalyst were systemically studied by structure characterizations, activity tests and thermodynamic calculations under different temperature. The results revealed that the structures and anti-coking properties of the nanocomposite catalyst primarily depended on reaction temperature. The in-situ XRD, H-2 chemisorption and TEM analysis of the catalysts indicated that only slightly sintering of Ni and ZrO2 took place at a lower reduction and reaction temperature (750 degrees C). At a higher reduction and reaction temperature (850 degrees C), severe sintering of ZrO2 and Ni was observed. However, it is interesting to find that the formed large nickel particles were almost covered by ZrO2 support after the high temperature reduction and only exposed very small nickel size. Coking analysis revealed that although a small Ni size could kinetically inhibit the carbon formation to some extent, a relatively higher amount of coking was formed at 750 degrees C due to the strong thermodynamic tendency for coking. At 850 degrees C, the amount of carbon deposition was much lower than that at 750 degrees C, which was mainly attributed to the unfavorable coking thermodynamics and the small exposed size of Ni. Therefore, high reaction temperature resulted in both the thermodynamic and kinetic coking inhibition behaviors and contributed to the superior anti-coking performance of the nanocomposite catalyst. It is our belief that the results obtained in this work could provide valuable implications for optimizing catalyst structure and reaction condition to achieve coking-free DRM catalysts and processes. (C) 2017 Elsevier B.V. All rights reserved.
引用
收藏
页码:63 / 73
页数:11
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