The objective of this article is to demonstrate significant efficiency and performance improvements by simple process modifications of a power to gas plant consisting of high‐temperature coelectrolysis and catalytic methanation. For the advanced process design dual step methanation with two different pressure levels including intermediate compression is proposed, leading to several advantages. By experimental investigations on a lab‐scale methanation test plant higher turnovers (increase of up to 7.1 percentage points) and lower temperature peaks (decrease by up to 130 K) can be proven. Basic energy balance calculations reveal furthermore a reduction in compressor power by 42% for this proposed system.
The energy supply in Austria is significantly based on fossil natural gas. Due to the necessary decarbonization of the heat and energy sector, a switch to a green substitute is necessary to limit CO2 emissions. Especially innovative concepts such as power-to-gas establish the connection between the storage of volatile renewable energy and its conversion into green gases. In this paper, different methanation strategies are applied on syngas from biomass gasification. The investigated syngas compositions range from traditional steam gasification, sorption-enhanced reforming to the innovative CO2 gasification. As the producer gases show different compositions regarding the H2/COx ratio, three possible methanation strategies (direct, sub-stoichiometric and over-stoichiometric methanation) are defined and assessed with technological evaluation tools for possible future large-scale set-ups consisting of a gasification, an electrolysis and a methanation unit. Due to its relative high share of hydrogen and the high technical maturity of this gasification mode, syngas from steam gasification represents the most promising gas composition for downstream methanation. Sub-stoichiometric operation of this syngas with limited H2 dosage represents an attractive methanation strategy since the hydrogen utilization is optimized. The overall efficiency of the sub-stoichiometric methanation lies at 59.9%. Determined by laboratory methanation experiments, a share of nearly 17 mol.% of CO2 needs to be separated to make injection into the natural gas grid possible. A technical feasible alternative, avoiding possible carbon formation in the methanation reactor, is the direct methanation of sorption-enhanced reforming syngas, with an overall process efficiency in large-scale applications of 55.9%.
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