@misc{GonzalezCastanoIvanovaIoanidesetal., author = {Gonz{\´a}lez-Casta{\~n}o, Miriam and Ivanova, Svetlana and Ioanides, Theophiles and Centeno, Miguel Angel and Arellano-Garc{\´i}a, Harvey and Odriozola, Jos{\´e} Antonio}, title = {Zr and Fe on Pt/CeO2-MOx/Al2O3 catalysts for WGS reaction}, series = {International Journal of Energy Research}, journal = {International Journal of Energy Research}, issn = {1099-114X}, doi = {10.1002/er.6646}, pages = {12}, abstract = {By evaluating the functional modifications induced by Zr and Fe as dopants in Pt/CeO2-MOx/Al2O3 catalysts (M = Fe and Zr), the key features for improving water gas shift (WGS) performance for these systems have been addressed. Pt/ceria intrinsic WGS activity is often related to improved H2 surface dynamics, H2O absorption, retentions and dissociation capacities which are influenced greatly by the support nature. Two metals, iron and zirconia, were chosen as ceria dopants in this work, either in separate manner or combined. Iron incorporation resulted in CO-redox properties and oxygen storage capacities (OSC) improvement but the formation of Ce-Fe solid solutions did not offer any catalytic benefit, while the Zr incorporation influenced in a great manner surface electron densities and shows higher catalytic activity. When combined both metals showed an important synergy evidenced by 30\% higher CO conversions and attributed to greater surface electron densities population and therefore absorption and activity. This work demonstrates that for Pt/ceria catalysts OSC enhancement does not necessarily imply a catalytic promotion.}, language = {en} } @misc{BaenaMorenoGonzalezCastanoNavarrodeMigueletal., author = {Baena-Moreno, Francisco Manuel and Gonz{\´a}lez-Casta{\~n}o, Miriam and Navarro de Miguel, Juan Carlos and Miah, Kamal Uddin Mohammad and Ossenbrink, Ralf and Odriozola, Jos{\´e} Antonio and Arellano-Garc{\´i}a, Harvey}, title = {Stepping toward Efficient Microreactors for CO2 Methanation: 3D Printed Gyroid Geometry}, series = {ACS Sustainable Chemistry \& Engineering}, volume = {9}, journal = {ACS Sustainable Chemistry \& Engineering}, number = {24}, issn = {2168-0485}, doi = {10.1021/acssuschemeng.1c01980}, pages = {8198 -- 8206}, abstract = {This work presents a comparative study towards the development of efficient micro-reactors based on 3D-printed structures. Thus, the study evaluates the influence of the metal substrate geometry on the performance of structured catalysts for the CO2 methanation reaction. For this purpose, 0.5\%Ru-15\%Ni/MgAl2O4 catalyst is wash coated over two different micro-monolithic metal substrates: a conventional parallel channel honeycomb structure and a novel 3D-printed structure with a complex gyroid geometry. The effect of the metal substrate geometry is analyzed for several CO2 sources including ideal flue gas atmospheres, the presence of residual CH4 and CO in the flue gas, as well as simulated biogas sources. The advantages of the gyroid-3D complex geometries over the honeycomb structures are shown for all evaluated conditions, providing at the best-case scenario a 14\% improvement of CO2 conversion. Moreover, this contribution shows that systematically tailoring geometrical features of structured catalysts becomes an effective strategy to achieve improved catalysts performances independent of the flue gas composition. By enhancing the transport processes and the gas-catalyst interactions, the employed gyroid 3D metal substrates enable boosted CO2 conversions and greater CH4 selectivity within diffusional controlled regimes.}, language = {en} } @misc{GonzalezCastanoNavarrodeMiguelPernkovaetal., author = {Gonz{\´a}lez-Casta{\~n}o, Miriam and Navarro de Miguel, Juan Carlos and Pernkova, A. and Centeno, Miguel Angel and Odriozola, Jos{\´e} Antonio and Arellano-Garc{\´i}a, Harvey}, title = {Ni/YMnO3 perovskite catalyst for CO2 methanation}, series = {Applied Materials Today}, volume = {23}, journal = {Applied Materials Today}, doi = {10.1016/j.apmt.2021.101055}, abstract = {Ni/YMnO3 perovskite catalyst for CO2 methanation}, language = {en} } @misc{MahmoodGonzalezCastanoPenkovaetal., author = {Mahmood, Safdar and Gonz{\´a}lez-Casta{\~n}o, Miriam and Penkova, Anna and Centeno, Miguel Angel and Odriozola, Jos{\´e} Antonio and Arellano-Garc{\´i}a, Harvey}, title = {CO2 methanation on Ni/YMn1-xAlxO3 perovskite catalysts}, series = {Applied Materials Today}, volume = {29}, journal = {Applied Materials Today}, issn = {2352-9407}, doi = {10.1016/j.apmt.2022.101577}, pages = {1 -- 11}, abstract = {Seeking for advanced catalytic systems for the CO2 methanation reaction, the use of Ni supported catalysts over redox materials is often proposed. Profiting the superior redox properties described for layered perovskite systems, this work has investigated a series Ni supported YMn1-xAlxO3 (x = 0, 0.2, 0.5, 0.8, 1) perovskite catalysts. The obtained results evidenced the impact of the support nature on the systems redox properties and Ni-support interactions. Within the catalysts series, the greater methanation rates displayed by Ni/YMn0.5Al0.5O3 catalyst (0.748 mmolCO2,conv.s-1 gNi -1 at 400 ◦C and 60 L/gh) were associated to the interplay between the support redox properties and superior Ni dispersion. The improved redox behavior attained through the Al-incorporation (up to x = 0.5) was associated to the layered perovskite structures which, being distorted and constituted by smaller crystal sizes, facilitated the behavior of Mn redox couples as surface species readily interconverted. Exhibiting catalytic performances comparable to precious metals based catalysts, this work proposes the Ni/YMn0.5Al0.5O3 catalyst as an effective system for the CO2 methanation reaction.}, language = {en} } @misc{GonzalezCastanoBaenaMorenoNavarrodeMigueletal., author = {Gonz{\´a}lez-Casta{\~n}o, Miriam and Baena-Moreno, Francisco Manuel and Navarro de Miguel, Juan Carlos and Miah, Kamal Uddin Mohammad and Arroyo-Torralvo, F{\´a}tima and Ossenbrink, Ralf and Odriozola, Jos{\´e} Antonio and Benzinger, Walther and Hensel, Andreas and Wenka, Achim and Arellano-Garc{\´i}a, Harvey}, title = {3D-printed structured catalysts for CO2 methanation reaction: Advancing of gyroid-based geometries}, series = {Energy Conversion and Management}, volume = {258}, journal = {Energy Conversion and Management}, issn = {2590-1745}, doi = {10.1016/j.enconman.2022.115464}, pages = {8}, abstract = {This work investigates the CO2 methanation rate of structured catalysts by tuning the geometry of 3D-printed metal Fluid Guiding Elements (FGEs) structures based on periodically variable pseudo-gyroid geometries. The enhanced performance showed by the structured catalytic systems is mostly associated with the capability of the FGEs substrate geometries for efficient heat usages. Thus, variations on the channels diameter resulted in ca. 25\% greater CO2 conversions values at intermediate temperature ranges. The highest void fraction evidenced in the best performing catalyst (3D-1) favored the radial heat transfer and resulted in significantly enhanced catalytic activity, achieving close to equilibrium (75\%) conversions at 400 ◦C and 120 mL/min. For the 3D-1 catalyst, a mathematical model based on an experimental design was developed thus enabling the estimation of its behavior as a function of temperature, spatial velocity, hydrogen to carbon dioxide (H2/CO2) ratio, and inlet CO2 concentration. Its optimal operating conditions were established under 3 different scenarios: 1) no restrictions, 2) minimum H2:CO2 ratios, and 3) minimum temperatures and H2/CO2 ratio. For instance, for the lattest scenario, the best CO2 methanation conditions require operating at 431 ◦C, 200 mL/min, H2/CO2 = 3 M ratio, and inlet CO2 concentration = 10 \%.}, language = {en} }