Chemistry:Methanation
Methanation is the conversion of carbon monoxide and carbon dioxide (COx) to methane (CH4) through hydrogenation. The methanation reactions of COx were first discovered by Sabatier and Senderens in 1902.[1]
COx methanation has many practical applications. It is a means of carbon oxide removal from process gases and is also being discussed as an alternative to PROX in fuel processors for mobile fuel cell applications.[2]
Methanation as a means of producing synthetic natural gas has been considered since the 1970s.[1] More recently it has been considered as a way to store energy produced from solar or wind power using power-to-gas systems in conjunction with existing natural gas storage.
Chemical reactions
The following reactions describe the methanation of carbon monoxide and carbon dioxide respectively:
- [math]\ce{ CO + 3H2 -> CH4 + H2O }[/math] -206 kJ/mol
- [math]\ce{ CO2 + 4H2 -> CH4 + 2 H2O }[/math] -164 kJ/mol
The methanation reactions are classified as exothermic and their energy of formations are listed.[1]
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] CO is believed to be methanated 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 reaction over different carried metal catalysts including Ni,[4] Ru[5] and Rh[6] has been widely investigated for the production of CH4 from syngas and other power to gas initiatives.[3] Nickel is the most widely used catalyst due to its high selectivity and low cost.[1]
Industrial applications
Creation of synthetic natural gas
Methanation is an important step in the creation of synthetic or substitute natural gas (SNG).[7] Coal or wood undergo gasification which creates a producer gas that must undergo methanation in order to produce a usable gas that just needs to undergo a final purification step.
The first commercial synthetic gas plant opened in 1984 and is the Great Plains Synfuel plant in Beulah, North Dakota.[1] It is still operational and produces 1500 MW worth of SNG using coal as the carbon source. In the years since its opening, other commercial facilities have been opened using other carbon sources such as wood chips.[1]
In France, the AFUL Chantrerie, located in Nantes, started in November 2017 the demonstrator MINERVE. This methanation unit of 14 Nm3/day was carried out by Top Industrie, with the support of Leaf. This installation is used to feed a CNG station and to inject methane into the natural gas boiler.[8]
Ammonia synthesis
In ammonia production CO and CO2 are considered poisons to most commonly used catalysts.[9] Methanation catalysts are added after several hydrogen producing steps to prevent carbon oxide buildup in the ammonia synthesis loop as methane does not have similar adverse effects on ammonia synthesis rates.
See also
References
- ↑ 1.0 1.1 1.2 1.3 1.4 1.5 Rönsch, 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. doi:10.1016/j.fuel.2015.10.111.
- ↑ Men, Yong; Kolb, Gunther; Zapf, Ralf; Hessel, Volker; Löwe, Holger (2007). "Selective methanation of carbon oxides in a microchannel reactor—Primary screening and impact of gas additives" (in en). Catalysis Today 125 (1–2): 81–87. doi:10.1016/j.cattod.2007.02.017.
- ↑ 3.0 3.1 Miao, Bin; Ma, Su Su Khine; Wang, Xin; Su, Haibin; Chan, Siew Hwa (2016-06-13). "Catalysis mechanisms of CO2 and CO methanation" (in en). Catalysis Science & Technology 6 (12): 4048. doi:10.1039/C6CY00478D. ISSN 2044-4761. http://pubs.rsc.org/-/content/articlehtml/2016/cy/c6cy00478d.
- ↑ Xavier, K. O; Sreekala, R; Rashid, K. K. A; Yusuff, K. K. M; Sen, B (1999-02-24). "Doping effects of cerium oxide on Ni/Al2O3 catalysts for methanation" (in en). Catalysis Today 49 (1): 17–21. doi:10.1016/S0920-5861(98)00403-9. ISSN 0920-5861.
- ↑ Utaka, T (2003-06-25). "CO removal from reformed fuels over Cu and precious metal catalysts" (in en). Applied Catalysis A: General 246 (1): 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" (in en). Applied Catalysis A: General 344 (1–2): 45–54. doi:10.1016/j.apcata.2008.03.039.
- ↑ Kopyscinski, Jan; Schildhauer, Tilman J.; Biollaz, Serge M. A. (2010-08-01). "Production of synthetic natural gas (SNG) from coal and dry biomass – A technology review from 1950 to 2009". Fuel 89 (8): 1763–1783. doi:10.1016/j.fuel.2010.01.027.
- ↑ "Un démonstrateur Power to gas en service à Nantes" (in fr). 2018. https://www.lemoniteur.fr/article/un-demonstrateur-power-to-gas-en-service-a-nantes-35321848..
- ↑ Khorsand, Kayvan (2007). "Modeling and simulation of methanation catalytic reactor in ammonia unit". Petroleum & Coal 49: 46–53. https://www.researchgate.net/publication/26498529.
![]() | Original source: https://en.wikipedia.org/wiki/Methanation.
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