Catalytic Steam and Partial Oxidation Reforming of Liquid Fuels for Application in Improving the Efficiency of Internal Combustion Engines

D. William Brookshear, Josh A. Pihl, James P. Szybist

Research output: Contribution to journalArticlepeer-review

25 Scopus citations

Abstract

This study investigated the potential for catalytically reforming liquid fuels in a simulated exhaust gas recirculation (EGR) mixture loop for the purpose of generating reformate that could be used to increase stoichiometric combustion engine efficiency. The experiments were performed on a simulated exhaust flow reactor using a Rh/Al2O3 reformer catalyst, and the fuels evaluated included iso-octane, ethanol, and gasoline. Both steam reforming and partial oxidation reforming were examined as routes for the production of reformate. Steam reforming was determined to be an ineffective option for reforming in an EGR loop, because of the high exhaust temperatures (in excess of 700 °C) required to produce adequate concentrations of reformate, regardless of fuel. However, partial oxidation reforming is capable of producing hydrogen concentrations as high as 10%-16%, depending on fuel and operating conditions in the simulated EGR gas mixture. Meanwhile, measurements of total fuel enthalpy retention were shown to have favorable energetics under a range of conditions, although a tradeoff between fuel enthalpy retention and reformate production was observed. Of the three fuels evaluated, iso-octane exhibited the best overall performance, followed by ethanol and then gasoline. Overall, it was found that partial oxidation reforming of liquid fuels in a simulated EGR mixture over the Rh/Al2O3 catalyst demonstrated sufficiently high reformate yields and favorable energetics to warrant further evaluation in the EGR system of a stoichiometric combustion engine.

Original languageEnglish
Pages (from-to)2267-2281
Number of pages15
JournalEnergy and Fuels
Volume32
Issue number2
DOIs
StatePublished - Feb 15 2018

Funding

This research was supported by the U.S. Department of Energy Office of Energy Efficiency and Renewable Energy, Vehicle Technologies Office. The authors gratefully acknowledge the support and guidance of program managers Gurpreet Singh and Michael Weismiller at DOE. The authors also gratefully acknowledge John Nunan (Umicore) for providing catalyst samples and Galen Fisher (University of Michigan) for supporting our efforts to obtain substrates and catalysts. This research was supported by the U.S. Department of Energy, Office of Energy Efficiency and Renewable Energy, Vehicle Technologies Office. The authors gratefully acknowledge the support and guidance of program managers Gurpreet Singh and Michael Weismiller at DOE. The authors also gratefully acknowledge John Nunan (Umicore) for providing catalyst samples and Galen Fisher (University of Michigan) for supporting our efforts to obtain substrates and catalysts.

FundersFunder number
U.S. Department of Energy
Office of Energy Efficiency and Renewable Energy
University of Michigan
Vehicle Technologies Office

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