Methane Steam Reforming on the Pt/CeO2 Catalyst: Effect of Daily Start-Up and Shut-Down on Long-Term Stability of the Catalyst

被引:29
作者
Amjad, Um-e-Salma [1 ,2 ]
Quintero, Carmen W. Moncada [2 ]
Ercolino, Giuliana [2 ]
Italiano, Cristina [3 ]
Vita, Antonio [3 ]
Specchia, Stefania [2 ,3 ]
机构
[1] COMSATS Univ, Dept Chem Engn, Islamabad Lahore Campus,Def Rd,Off Raiwind Rd, Lahore 54000, Pakistan
[2] Politecn Torino, Dept Appl Sci & Technol, Corso Duca Abruzzi 24, I-10129 Turin, Italy
[3] CNR ITAE Nicola Giordano, Via Salita S Lucia Sopra Contesse 5, I-98126 Messina, Italy
基金
欧盟第七框架计划;
关键词
WATER-GAS-SHIFT; SOLUTION COMBUSTION SYNTHESIS; HYDROGEN-PRODUCTION; PARTIAL OXIDATION; CEO2; CATALYST; N-DODECANE; PERFORMANCE; TEMPERATURE; REDUCTION; NANOSTRUCTURES;
D O I
10.1021/acs.iecr.9b02436
中图分类号
TQ [化学工业];
学科分类号
0817 ;
摘要
An environmentally friendly auxiliary power unit requires catalysts operating in the cyclic mode, producing H-2 at a steady rate with high CO2 selectivity and minimum CO clean-up. Here, 1% Pt/CeO2 catalyst was synthesized using the solution combustion synthesis method and investigated toward methane steam reforming reaction. Preliminary tests were performed by varying the steam-to-carbon ratio (S/C), gas hourly space velocity (GHSV), and time-on-stream (TOS). The catalyst showed near equilibrium CH4 conversion and high H-2 concentration (75% dry basis, N-2-free) obtained at S/C = 2.8 and GHSV = 24 000 h(-1). The catalytic activity was stable after 25 cycles of start-up and shut-down operations, equivalent to 150 h of TOS. X-ray diffraction, transmission electron microscopy, and X-ray photoelectron spectroscopy techniques were used to characterize either the fresh and aged catalyst after 150 h of TOS.
引用
收藏
页码:16395 / 16406
页数:12
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