dc.contributor
Universitat Politècnica de Catalunya. Departament d'Enginyeria Química
dc.contributor
Universitat Politècnica de Catalunya. Doctorat en Polímers i Biopolímers
dc.contributor
Universitat Politècnica de Catalunya. Departament de Física
dc.contributor
Universitat Politècnica de Catalunya. IMEM-BRT- Innovation in Materials and Molecular Engineering - Biomaterials for Regenerative Therapies
dc.contributor
Universitat Politècnica de Catalunya. PSEP - Polimers Sintètics: Estructura i Propietats. Polimers Biodegradables
dc.contributor.author
Revilla López, Guillermo
dc.contributor.author
Sans Milà, Jordi
dc.contributor.author
Casanovas Salas, Jordi
dc.contributor.author
Bertran Cànovas, Òscar
dc.contributor.author
Puiggalí Bellalta, Jordi
dc.contributor.author
Turon, Pau
dc.contributor.author
Alemán Llansó, Carlos
dc.date.issued
2020-04-25
dc.identifier
Revilla-López, G. [et al.]. Analysis of nitrogen fixation by a catalyst capable of transforming N2, CO2 and CH4 into amino acids under mild reactions conditions. "Applied catalysis A. General", 25 Abril 2020, vol. 596, p. 1-9.
dc.identifier
https://hdl.handle.net/2117/342071
dc.identifier
10.1016/j.apcata.2020.117526
dc.description.abstract
The processes related to the fixation of nitrogen ina catalyst able to produce glycine and alanine from a N2, CO2and CH4gas mixture at mild reaction conditions have been studied by combining experimental and theoretical investigations.Results have allowed to understand the role of different elements of the catalyst, which is constituted by permanently polarized hydroxyapatite (p-HAp), zirconia, and aminotris(methylenephosphonic acid)(ATMP). ATMP attractsN2moleculestowards the surface,maintainingthem close to the zirconiaand p-HAp componentsthatare the most active from a catalytic point of view. On the other hand, the associative mechanismisthermodynamicallyfavouredunder mild reaction conditionswith respect to the dissociative one,whichis limited by the barrier associated to the N–Nbondcleavage. Because this reaction mechanism is similar to that employed in the nitrogen fixation bynitrogenase enzymes, thesefindingsprovide an opportunity to designnew bioinspired catalysts
dc.description.abstract
Postprint (author's final draft)
dc.format
application/pdf
dc.relation
https://www.sciencedirect.com/science/article/abs/pii/S0926860X20301198
dc.subject
Àrees temàtiques de la UPC::Enginyeria química
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Photosynthesis
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Artificial photosynthesis
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carbon fixation
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hydroxyapatite
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N–N bond cleavage
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Nitrogen -- Fixació
dc.title
Analysis of nitrogen fixation by a catalyst capable of transforming N2, CO2 and CH4 into amino acids under mild reactions conditions