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用于甲烷蒸汽/二氧化碳联合重整的镍基催化剂上的积碳

Carbon Deposition Onto Ni-Based Catalysts for Combined Steam/CO2 Reforming of Methane.

作者信息

Li Peng, Park Yoon Hwa, Moon Dong Ju, Park Nam Cook, Kim Young Chul

出版信息

J Nanosci Nanotechnol. 2016 Feb;16(2):1562-6. doi: 10.1166/jnn.2016.12006.

Abstract

The present study was performed to suppress carbon deposition by Ce and Fe onto Ni-based catalysts in combined steam/CO2 reforming of methane (CSCRM), which is a process for producing synthesis gas (H2:CO = 2:1) for gas-to-liquids (GTL). The catalytic reaction was evaluated at 900 degrees C and 20 bar with a reactant feed ratio CH4:CO2:H20:Ar = 1:0.8:1.3:1 and gas hourly space velocity GHSV = 25,000 h(-1). The Ce and Fe modified Ni/gamma-A120, catalyst was characterized by BET surface area analysis, X-ray diffraction (XRD), H2 temperature-programmed reduction (TPR), H2 chemisorption, CO2 temperature-programmed desorption (TPD) and SEM. Ce- and Fe-modified Ni/Al2O3 catalysts exhibited remarkable activity and stability during the CSCRM over the course of 50 hours. It suggested that the Ni(12)-Ce(5)-Fe(5)/Al2O3 catalyst shows highly dispersed Ni particles with strong metal-to-support interaction (SMSI) as well as excellent catalytic activity.

摘要

本研究旨在抑制Ce和Fe在甲烷蒸汽/二氧化碳联合重整(CSCRM)过程中沉积在镍基催化剂上,该过程是一种用于生产气制液(GTL)合成气(H2:CO = 2:1)的工艺。在900℃和20巴的条件下,以反应物进料比CH4:CO2:H20:Ar = 1:0.8:1.3:1和气时空速GHSV = 25,000 h(-1)对催化反应进行了评估。通过BET表面积分析、X射线衍射(XRD)、H2程序升温还原(TPR)、H2化学吸附、CO2程序升温脱附(TPD)和扫描电子显微镜(SEM)对Ce和Fe改性的Ni/gamma-A120催化剂进行了表征。在50小时的CSCRM过程中,Ce和Fe改性的Ni/Al2O3催化剂表现出显著的活性和稳定性。这表明Ni(12)-Ce(5)-Fe(5)/Al2O3催化剂显示出高度分散的Ni颗粒,具有强的金属-载体相互作用(SMSI)以及优异的催化活性。

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