Integration of gasoline prereforming into autothermal reforming for hydrogen production

An integrated process for hydrogen production which couples gasoline prereforming and autothermal reforming (ATR) over nickel-based catalysts was investigated using stainless steel fixed-bed reactors. Meanwhile the integrated process was compared with the gasoline ATR process without prereforming. The results indicate that in the gasoline ATR process without prereforming, the nickel-based ATR catalyst deposited with coke after short reaction time-on-stream under the following working conditions (T = 770 degrees C, P = 5.0 bar, steam-to-carbon feed ratio (S/C, mol/mol) of 2.7, oxygen-to-carbon feed ratio (O-2/C) of 0.5 and gas hourly space velocity (GHSV) of 28,000 ml g(-1) h(-1)). Quite the contrary, in the integrated process, almost 100% gasoline conversion and 99.4% selectivity to hydrogen were obtained and maintained well under similar working conditions during 100 h reaction time-on-stream. Actually, almost coke-free operation of the process was achieved, which was confirmed by scanning electron microscopy (SEM) and O-2-TPSR characterizations of the used ATR catalyst. Reformate that contains no light alkenes or other higher hydrocarbons could be obtained from the ATR reactor. In addition, the nickel-based prereforming catalyst prepared by a coprecipitation method had high catalytic activity and promising stability. (C) 2006 Elsevier B.V. All rights reserved.

[1]  Detlef Stolten,et al.  Combination of autothermal reforming with water-gas-shift reaction—small-scale testing of different water-gas-shift catalysts , 2004 .

[2]  A. Ciajolo,et al.  Controlling steps in the low-temperature oxidation of n-heptane and iso-octane , 1998 .

[3]  John P. Kopasz,et al.  Fuel processing for fuel cell systems in transportation and portable power applications , 2002 .

[4]  Jens R. Rostrup-Nielsen,et al.  Steam reforming of liquid hydrocarbons , 1998 .

[5]  Guy Marin,et al.  Kinetic Modeling of Coke Formation during Steam Cracking , 2002 .

[6]  R. Ran,et al.  Low-temperature partial oxidation of n-heptane to CO+H2 over Rh-based/γ-Al2O3 catalysts , 2004 .

[7]  Ryuji Kikuchi,et al.  Catalytic autothermal reforming of methane and propane over supported metal catalysts , 2003 .

[8]  J. Armor,et al.  The multiple roles for catalysis in the production of H2 , 1999 .

[9]  P. Pfeifer,et al.  Temperature profiles and residence time effects during catalytic partial oxidation and oxidative steam reforming of propane in metallic microchannel reactors , 2005 .

[10]  C. H. Bartholomew Mechanisms of catalyst deactivation , 2001 .

[11]  Hengyong Xu,et al.  Characterizations and activities of the nano-sized Ni/Al2O3 and Ni/La-Al2O3 catalysts for NH3 decomposition , 2005 .

[12]  John P. Kopasz,et al.  Unraveling the maze: Understanding of diesel reforming through the use of simplified fuel blends☆ , 2005 .

[13]  Tiziano Faravelli,et al.  Lumping procedures in detailed kinetic modeling of gasification, pyrolysis, partial oxidation and combustion of hydrocarbon mixtures , 2001 .

[14]  H. Brunner,et al.  Catalytic Partial Oxidation of n-Heptane for Hydrogen Production , 2003 .

[15]  Thomas Sandahl Christensen,et al.  Adiabatic prereforming of hydrocarbons — an important step in syngas production , 1996 .

[16]  Sang Deuk Lee,et al.  Studies on gasoline fuel processor system for fuel-cell powered vehicles application , 2001 .

[17]  B. Steele,et al.  Materials for fuel-cell technologies , 2001, Nature.

[18]  H. Schaper,et al.  The influence of lanthanum oxide on the thermal stability of gamma alumina catalyst supports , 1983 .