Catalytic bi-reforming of methane: from greenhouse gases to syngas
- Louisiana State Univ., Baton Rouge, LA (United States)
- KTH Royal Inst. of Technology, Stockholm (Sweden)
The bi-reforming reaction to produce syngas from CH4 and CO2 offers significant advantages over dry reforming and oxy-CO2 with respect to catalyst deactivation by carbonization. This approach has potential for powerful new alternatives and is entering the stage of increasing advanced research toward commercialization of the technology. Research is ongoing to develop catalysts that are resistant to high temperatures and the presence of a more oxidative environment due to steam. All current research on bi-reforming catalysis is focused on Ni-based catalysts, a logical extension based on commercial materials on steam/methane reforming and dry reforming. However, we report recent work on thermally stable crystalline oxides has promise, particularly in resisting carbon deposition while remaining stable at the demanding conditions of bi-reforming.
- Research Organization:
- Energy Frontier Research Centers (EFRC) (United States). Center for Atomic-Level Catalyst Design (CALCD)
- Sponsoring Organization:
- USDOE Office of Science (SC), Basic Energy Sciences (BES)
- Grant/Contract Number:
- SC0001058
- OSTI ID:
- 1369696
- Alternate ID(s):
- OSTI ID: 1356686
- Journal Information:
- Current Opinion in Chemical Engineering, Vol. 9, Issue C; Related Information: CALCD partners with Louisiana State University (lead); Clemson University; University of Florida; Georgia Institute of Technology; Grambling State University; Oak Ridge National Laboratory; Ohio State University; Pennsylvania State; Texas A&M University; Vienna University of Technology, Austria; University of Utrecht, Netherlands; ISSN 2211-3398
- Publisher:
- ElsevierCopyright Statement
- Country of Publication:
- United States
- Language:
- English
Web of Science
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