Abstract <p>Non-thermal plasma (NTP) enables non-equilibrium activation of CH<sub>4</sub> and CO<sub>2</sub> under mild conditions, offering an alternative route for low-temperature gas-to-liquid conversion. In this work, methane bi-reforming (CH<sub>4</sub>/H<sub>2</sub>O/CO<sub>2</sub> = 3 : 2 : 1) to methanol was investigated over Cu-based catalysts in a dielectric barrier discharge (DBD) reactor under three configurations: thermal catalysis (no plasma), in-plasma catalysis (IPC), and post-plasma catalysis (PPC). Experiments were conducted at atmospheric pressure with discharge power ranging from 30 to 60 W, corresponding to a specific energy input (SEI) of 15‒30 J/cm<sup>3</sup>. Discharge power was quantified using the Lissajous method. Among the tested configurations, IPC exhibited the best performance, achieving CH<sub>4</sub> and CO<sub>2</sub> conversions of 35 and 30%, respectively, a space-time yield of 3.6 mmol g<sup>–1</sup> h<sup>–1</sup>, and an energy efficiency of 5.5% at SEI ≈ 22 J/cm<sup>3</sup>. In contrast, IPC showed higher conversion but lower stability and MeOH selectivity relative to PPC due to direct plasma-catalyst interaction. These results demonstrate that spatial separation of plasma and catalyst effectively enhances methanol selectivity and stability, providing design guidance for compact and decentralized plasma-assisted GTL processes.</p>

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Non-Thermal Plasma Assisted Methane Reforming to Methanol over Cu-Based Catalysts

  • Nabil Majd Alawi,
  • Ho Hong Quyen,
  • Hoang M. Nguyen,
  • Jamal M. Ali,
  • Ouf A. Shams

摘要

Abstract

Non-thermal plasma (NTP) enables non-equilibrium activation of CH4 and CO2 under mild conditions, offering an alternative route for low-temperature gas-to-liquid conversion. In this work, methane bi-reforming (CH4/H2O/CO2 = 3 : 2 : 1) to methanol was investigated over Cu-based catalysts in a dielectric barrier discharge (DBD) reactor under three configurations: thermal catalysis (no plasma), in-plasma catalysis (IPC), and post-plasma catalysis (PPC). Experiments were conducted at atmospheric pressure with discharge power ranging from 30 to 60 W, corresponding to a specific energy input (SEI) of 15‒30 J/cm3. Discharge power was quantified using the Lissajous method. Among the tested configurations, IPC exhibited the best performance, achieving CH4 and CO2 conversions of 35 and 30%, respectively, a space-time yield of 3.6 mmol g–1 h–1, and an energy efficiency of 5.5% at SEI ≈ 22 J/cm3. In contrast, IPC showed higher conversion but lower stability and MeOH selectivity relative to PPC due to direct plasma-catalyst interaction. These results demonstrate that spatial separation of plasma and catalyst effectively enhances methanol selectivity and stability, providing design guidance for compact and decentralized plasma-assisted GTL processes.