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The development of autothermal microchannel reactor technology for hydrogen-based gas processing

dc.contributor.advisorEverson, R.C.
dc.contributor.authorEngelbrecht, Nicolaas
dc.contributor.researchID10168249 - Everson, Raymond Cecil (Supervisor)
dc.date.accessioned2022-03-08T14:26:40Z
dc.date.available2022-03-08T14:26:40Z
dc.date.issued2021
dc.descriptionDEng (Chemical Engineering), North-West University, Potchefstroom Campusen_US
dc.description.abstractKey challenges associated with the production, transport, storage and continuous use of hydrogen (H2), generated from renewable energy, is the natural intermittency of some renewable resources such as solar photovoltaic and wind, and the physical properties of H2 that complicates its handling in the industry, i.e. its low volumetric energy density and high flammability. The work presented in this thesis demonstrates the use of process intensifying microchannel reactor technology for the thermo-catalytic processing of renewable H2 via attractive energy carriers: (i) the decomposition of ammonia (NH3) to form H2, as well as (ii) the synthesis of methane (CH4) using renewable H2 as feedstock (CO2 methanation). Furthermore, these processes require heat management strategies for effective autothermal operation. The NH3 decomposition reaction is endothermic and a coupled exothermic process (NH3 oxidation) is demonstrated to provide the heating requirements for H2 release. Conversely, the CO2 methanation process is exothermic, and cooling is required to reach equilibrium favouring reaction temperatures that promote the conversion of H2 and CO2 towards CH4. Extensive experimental investigations were carried out into these thermally coupled processes, and reported on for NH3 decomposition and for CO2 methanation. Then an evaluation of a compact methanation demonstrator unit incorporating the microchannel-based reactor was carried out, followed by computational fluid dynamic (CFD) modelling to evaluate associated heat and mass transport properties in the microchannel reactor. The scale of the microchannel reactors investigated here was such that NH3 up to a flow rate of 6 NL min-1 was processible towards H2 at a high conversion rate (99.8%), and corresponding to an equivalent H2 fuel cell power of 0.71 kWe, while total methanation flow rates of up to 7 NL min-1 were used to demonstrate CO2 methanation (90.5% CO2 conversion). Respective thermal efficiencies of 75.9% and 76.6% were obtained at the recommended steady-state operating points, which were close to thermodynamic equilibrium. These thermal efficiencies are deemed remarkable, considering the compact- and R&D-scale reactor technologies investigated herein. Overall, the work described in this thesis contributes to the development of micro-engineered reactors that are multifunctional catalytic conversion units and heat exchangers, and which support modular technologies for the processing of renewable H2.en_US
dc.description.thesistypeDoctoralen_US
dc.identifier.urihttps://orcid.org/0000-0001-8437-7427
dc.identifier.urihttp://hdl.handle.net/10394/38841
dc.language.isoenen_US
dc.publisherNorth-West University (South Africa).en_US
dc.subjectMicrochannel reactor technologyen_US
dc.subjectProcess intensificationen_US
dc.subjectThermally self-sustained processesen_US
dc.subjectPower-to-X concepten_US
dc.subjectRenewable hydrogenen_US
dc.subjectAmmonia-to-hydrogenen_US
dc.subjectCO2 methanationen_US
dc.titleThe development of autothermal microchannel reactor technology for hydrogen-based gas processingen_US
dc.typeThesisen_US

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