Kinetic study of the methane dry (CO2) reforming reaction over the Ce0.70La0.20Ni0.10O2−δ catalyst. Issue 8 (8th April 2020)

• Record Type: Journal Article
• Authors: Pino, Lidia; Italiano, Cristina; Laganà, Massimo; Vita, Antonio; Recupero, Vincenzo
• Is Part Of: Catalysis science & technology. Volume 10:Issue 8(2020)
• Page Start: 2652
• Page End: 2662
• Publication Date: 2020-04-08
• Subjects: Catalysis -- Periodicals; 541.395
• DOI: 10.1039/c9cy02192b
• Languages: English
• ISSNs: 2044-4753

Abstract

Abstract : The kinetic behaviour of the Ce0.70 La0.20 Ni0.10 O2− δ catalyst during the methane dry reforming reaction was investigated in a fixed bed reactor in the temperature range of 923–1023 K with the partial pressure of CH4 and CO2 ranging between 5 and 50 kPa. Abstract : The kinetic behaviour of the Ce0.70 La0.20 Ni0.10 O2− δ catalyst during the methane dry reforming reaction was investigated in a fixed bed reactor in the temperature range of 923–1023 K with the partial pressure of CH4 and CO2 ranging between 5 and 50 kPa. The experimental data were fitted using the empirical power-law rate equation and Langmuir–Hinshelwood kinetic models proposed in literature for the Ni–La2 O3 catalytic system and based on two-step single- and dual-site mechanisms. The obtained fitting results, after statistical and thermodynamic discrimination, showed that the mechanism of the dry reforming reaction over the Ce0.70 La0.20 Ni0.10 O2− δ catalyst could be successfully described by the two-step dual-site mechanism. The activation energies for the CH4 consumption from the power law and Langmuir–Hinshelwood models were estimated to be 91.5 and 136.9 kJ mol −1, respectively. The lower activation energies for the CO2 consumption (70.2 and 100.6 kJ mol −1 from both models) suggested that the CO2 activation should faster than CH4 . The basic nature of the Ce–La–O sites catalyzed the CO2 conversion to oxy-carbonate, decreasing the CO2 activation energy compared to that of CH4 .