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dc.contributor.authorAframehr, Wrya Mohammadi
dc.contributor.authorPfromm, Peter H.
dc.date.accessioned2022-11-21T19:27:06Z
dc.date.available2022-11-21T19:27:06Z
dc.date.issued2021-04-23
dc.identifier.citationWrya Mohammadi Aframehr and Peter H. Pfromm. 2021. Activating dinitrogen for chemical looping ammonia synthesis: nitridation of manganese. Journal of Materials Science 56: 12584-12595.en_US
dc.identifier.urihttp://hdl.handle.net/1808/33690
dc.description.abstractThe earth-abundant transition metal manganese (Mn) has been shown to be useful to activate dinitrogen at atmospheric pressure and elevated temperature by forming bulk Mn nitrides. Mn nitrides could then be used, for example, for ammonia (NH3) synthesis in a chemical looping process by contacting nitride with gaseous hydrogen (H2). Here, we present an investigation of the morphology and local time-dependent composition of micrometer-scale Mn plates during nitridation in dinitrogen (N2) near atmospheric pressure at 700 °C. The main motivation was to obtain design data for chemical looping synthesis of NH3 and to add to the somewhat sparse literature on nitridation of Mn. The morphology and elemental compositional variation of the nitrided specimens were studied with scanning electron microscopy (SEM), energy dispersive X-ray spectroscopy (EDX), wide angle X-ray diffraction (WAXD), and mass balances. Three possible nitrogen (N) populations that may govern the Mn nitridation and later NH3 synthesis are identified. After four hours of nitridation, the N weight gain was found to be 9.4 ± 0.7 kgN to nMn−1 for the plates used here, resulting in a nitridation depth of 83 ± 8 μm.en_US
dc.publisherJournal of Materials Scienceen_US
dc.relation.isversionofhttps://link.springer.com/article/10.1007/s10853-021-06079-7en_US
dc.titleActivating dinitrogen for chemical looping ammonia synthesis: nitridation of manganeseen_US
dc.typeArticleen_US
dc.identifier.doi10.1007/s10853-021-06079-7en_US
dc.identifier.orcidhttps://orcid.org/0000-0002-5028-7500en_US
dc.identifier.orcidhttps://orcid.org/0000-0003-4869-9503en_US
kusw.oaversionScholarly/refereed, publisher versionen_US
kusw.oapolicyThis item meets KU Open Access policy criteria.en_US
dc.rights.accessrightsopenAccessen_US


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