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Current understanding of Oxidative Coupling of Methane (OCM) reaction over supported Mn-Na2WO4 catalysts

Journal Article · · Catalysis Today
 [1];  [2];  [3]
  1. Indian Institute of Technology Madras, Chennai, Tamil Nadu (India); Lehigh Univ., Bethlehem, PA (United States); Idaho National Laboratory (INL), Idaho Falls, ID (United States)
  2. Idaho National Laboratory (INL), Idaho Falls, ID (United States)
  3. Lehigh Univ., Bethlehem, PA (United States)
This perspective reviews the current understanding of the Oxidative Coupling of Methane (OCM) reaction over the supported Mn-Na2WO4/SiO2 catalyst, with a focus on recent insights gained from state-of-the-art in-situ and operando spectroscopic characterization and chemical probe experiments under controlled environments. The supported Mn-Na2WO4/SiO2 catalyst exhibits dynamic structural changes during the OCM reaction, involving multiple reactive lattice and adsorbed oxygen species, each associated with different oxide phases. These oxygen species play distinct roles in various steps of the OCM mechanism. The catalytic active sites for activation of CH4 are associated with isolated surface Na-WOx sites on the SiO2 support and the role of surface MnOx sites on SiO2 is to oxidatively dehydrogenate C2H6 to C2H4. Furthermore, this paper provides a detailed discussion of these roles and also introduces new experimental data from Temporal Analysis of Products (TAP) studies to clarify the ongoing debate in the literature regarding the contributions of lattice versus adsorbed oxygen species in OCM reaction product formation. Additionally, recommendations are offered for optimizing the performance of supported Mn-Na2WO4/SiO2 catalysts to enhance CH4 activation and C2 product selectivity.
Research Organization:
Idaho National Laboratory (INL), Idaho Falls, ID (United States)
Sponsoring Organization:
Indian Institute of Technology Madras; National Science Foundation (NSF); USDOE Office of Energy Efficiency and Renewable Energy (EERE), Energy Efficiency Office. Advanced Materials & Manufacturing Technologies Office (AMMTO); USDOE Office of Energy Efficiency and Renewable Energy (EERE), Energy Efficiency Office. Industrial Efficiency & Decarbonization Office (IEDO); USDOE Office of Nuclear Energy (NE)
Grant/Contract Number:
AC07-05ID14517
OSTI ID:
3013708
Report Number(s):
INL/JOU--25-83877
Journal Information:
Catalysis Today, Journal Name: Catalysis Today Journal Issue: - Vol. 459; ISSN 0920-5861
Publisher:
ElsevierCopyright Statement
Country of Publication:
United States
Language:
English

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