StoppingClimateChange.com                                                                                                                    7.  Wood Syngas to Methane Upgrade
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Wood Syngas-to-Pipeline Grade Catalytic Methane Methanator   

 https://www.researchgate.net/publication/242263442_PRODUCTION_OF_BIO-METHANE_FROM_WOODY_BIOMASS/link/0046353317400db8bb000000/download

https://www.rti.org/news/rti-international-build-energy-technology-development-facility-support-biofuels-projects

About hydrogen - https://www.youtube.com/watch?v=f7MzFfuNOtY 

https://www.engineering-airliquide.com/steam-methane-reforming-hydrogen-production 

https://en.wikipedia.org/wiki/Steam_reforming 

Industrial reforming

Steam reforming of natural gas is the most common method of producing commercial bulk hydrogen at about 95% of the world production[1][2] of 500 billion m3 in 1998,[3] or 70 million tonnes by 2018.[4] Hydrogen is used in the industrial synthesis of ammonia and other chemicals.[5] At high temperatures (700 1100 C) and in the presence of a metal-based catalyst (nickel), steam reacts with methane to yield carbon monoxide and hydrogen.

CH4 + H2O CO + 3 H2

Catalysts with high surface-area-to-volume ratio are preferred because of diffusion limitations due to high operating temperature. Examples of catalyst shapes used are spoked wheels, gear wheels, and rings with holes. Additionally, these shapes have a low pressure drop which is advantageous for this application.[6]

Additional hydrogen can be obtained by reacting the CO with water via the water-gas shift reaction.

CO + H2O ⇌ CO2 + H2

The first reaction is strongly endothermic (consumes heat, ΔHr= 206 kJ/mol), the second reaction is mildly exothermic (produces heat, ΔHr= -41 kJ/mol).

For every tonne of hydrogen produced this way, 9 tonnes of CO2 is also produced.

Steam reforming of natural gas is approximately 6575% efficient.[9]

Production of H2 and CO from hydrocarbon gases (e.g. natural gas) is performed by two well-known "primary" and "secondary" reformers. Steam methane reforming (SMR) and autothermal reformer (ATR) are two industrial examples of the primary and secondary reformers, respectively. Each of which uses only special characteristics. On the other hand, the process of combined reforming utilizes both of primary and secondary tools for production of synthesis gas, as it is commonly practiced in ammonia manufacturing. For the case of methanol, ATR is fed with nearly pure oxygen (99.5%) rather than air since the presence of excessive N2 in the syngas would overburden compression and retard the methanol production. The ATR reformer consists of a partial oxidation (POX) chamber (usually non-catalytic medium) and a fixed bed catalytic section. The catalytic fixed bed not only adjusts the H2/CO ratio, but also destroys any probable soot and precursor (e.g. ethylene and acetylene) that may be formed in the POX chamber. Natural gas (NG) is partially oxidized in the combustion chamber by oxygen or air (as an oxidant). Steam to carbon (S/C) ratio that is usually 0.6 in the oxygen-based case has been commercialized by Haldor-Topose Company.

 

Another Possibility: