In the production of higher hydrocarbons, combining oxidative coupling of methane (OCM) with hydrogenation of the formed carbon oxides in a separate reactor provides an alternative to the currently applied methane conversion to syngas followed by Fischer‐Tropsch synthesis. The effects of CH4:O2 feed ratio in the OCM reactor and partial pressures of H2 or/and H2O in the hydrogenation reactor were analyzed to maximize production of C2+ hydrocarbons and reduce COx formation. The highest C2+ yield was achieved with low CH4:O2 feed ratio for OCM and removal of the formed water before entering the hydrogenation reactor.
Ni-catalyzed methanation has been discovered more than 100 years ago. Since then, many applications based on syngas -from coal or biomass -for the production of synthetic natural gas (SNG) have been established. Nevertheless, methanation still bears great potential for optimization. Especially for decentralized, biomass-based applications, decreased methanation temperatures and pressures are expected to lower the costs of the overall process. Consequently, it is necessary to obtain a catalyst that is highly active under such reduced reaction conditions. This objective was successfully reached by a systematic variation of reduction temperature, pressure, and hydrogen concentration under the aspects of the design of experiment within the catalyst activation process.
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