Hydrogen production via CO2 reforming of methane over ZrO2-Doped Ni/ZSM-5 nanostructured catalyst prepared by ultrasound assisted sequential impregnation method

被引:82
作者
Rahmani, Farhad [1 ,2 ]
Haghighi, Mohammad [1 ,2 ]
Vafaeian, Yaser [1 ,2 ]
Estifaee, Pooya [1 ,2 ]
机构
[1] Sahand Univ Technol, Fac Chem Engn, Sahand New Town, Tabriz, Iran
[2] Sahand Univ Technol, Reactor & Catalysis Res Ctr, Sahand New Town, Tabriz, Iran
关键词
CO2; reforming; Syngas; Hydrogen; Ni/ZSM-5-ZrO2; Ultrasound; NI-BASED CATALYSTS; SOL-GEL TECHNIQUE; CARBON-DIOXIDE; PHYSICOCHEMICAL CHARACTERIZATIONS; BENEFICIAL USE; SYNTHESIS GAS; NICKEL-CATALYSTS; SUPPORTED NI; NATURAL-GAS; NI/AL2O3-MGO NANOCATALYST;
D O I
10.1016/j.jpowsour.2014.08.123
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
In our continuing effort to find the proper catalyst for CO2 reforming of methane, Ni(8%)/ZSM-5-ZrO2 with various zirconium loadings (0-15%) are synthesized via sonochemical method. All samples are characterized by XRD, FESEM, TEM, EDX, BET, FTIR and TPR-H-2 techniques. The XRD results confirm existence of NiO, ZrO2 and ZSM-5 as crystalline phase in catalyst structure. FESEM images reveal small particle size of active metals and low numbers of agglomerations for Ni(8%)/ZrO2(5%)-ZSM-5. BET analysis shows that addition of ZrO2 to Ni/ZSM-5 decreases the surface area but Ni/ZrO2(5%)-ZSM-5 has the highest surface area. TEM analysis demonstrates high dispersion of Ni nano particles over the support. EDX depicts the best active metal dispersion for the catalyst with 5% zirconia loading. The TPR results prove that the metal-support interaction is enhanced by zirconia addition, indicating the better Ni dispersion. Apart from characterization, activity tests are performed and parameters such as effect of temperature, CO and H-2 yields and H-2/CO ratio are investigated. The results show that Ni(8%)/ZrO2(5%)-ZSM-5 has the best structural properties and the highest activity and stability in comparison with the other catalysts. (C) 2014 Elsevier B.V. All rights reserved.
引用
收藏
页码:816 / 827
页数:12
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