There is disagreement on whether the CO2 methanation occurs by first associatively adsorbing an adatom hydrogen and forming oxygen intermediates before hydrogenation or dissociating and forming a carbonyl before being hydrogenated.[3]
∆H = −206 kJ/mol
CO methanation is believed to occur through a dissociative mechanism where the carbon oxygen bond is broken before hydrogenation with an associative mechanism only being observed at high H2 concentrations.
Methanation reactions over different metal catalysts including Ni,[4] Ru[5] and Rh[6] have been widely investigated for the production of CH4 from syngas and other power to gas initiatives.[3] Nickel is the most widely used catalyst owing to its high selectivity and low cost.[2]
^ abRönsch, Stefan; Schneider, Jens; Matthischke, Steffi; Schlüter, Michael; Götz, Manuel; Lefebvre, Jonathan; Prabhakaran, Praseeth; Bajohr, Siegfried (2016-02-15). "Review on methanation – From fundamentals to current projects". Fuel. 166: 276–296. Bibcode:2016Fuel..166..276R. doi:10.1016/j.fuel.2015.10.111.
^ abMiao, Bin; Ma, Su Su Khine; Wang, Xin; Su, Haibin; Chan, Siew Hwa (2016-06-13). "Catalysis mechanisms of CO2 and CO methanation". Catalysis Science & Technology. 6 (12): 4048. doi:10.1039/C6CY00478D.
^Xavier, K.O; Sreekala, R.; Rashid, K.K.A; Yusuff, K.K.M; Sen, B. (1999). "Doping effects of cerium oxide on Ni/Al2O3 catalysts for methanation". Catalysis Today. 49 (1–3): 17–21. doi:10.1016/S0920-5861(98)00403-9.
^Utaka, Toshimasa; Takeguchi, Tatsuya; Kikuchi, Ryuji; Eguchi, Koichi (2003). "CO removal from reformed fuels over Cu and precious metal catalysts". Applied Catalysis A: General. 246: 117–124. doi:10.1016/S0926-860X(03)00048-6.
^Panagiotopoulou, Paraskevi; Kondarides, Dimitris I.; Verykios, Xenophon E. (2008). "Selective methanation of CO over supported noble metal catalysts: Effects of the nature of the metallic phase on catalytic performance". Applied Catalysis A: General. 344 (1–2): 45–54. doi:10.1016/j.apcata.2008.03.039.