TY - GEN A1 - González-Castaño, Miriam A1 - Ivanova, Svetlana A1 - Ioanides, Theophiles A1 - Centeno, Miguel Angel A1 - Arellano-García, Harvey A1 - Odriozola, José Antonio T1 - Zr and Fe on Pt/CeO2-MOx/Al2O3 catalysts for WGS reaction T2 - International Journal of Energy Research N2 - 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. KW - doped ceria KW - FE KW - H2-TPD KW - Pt/ceria catalysts KW - WGS reaction KW - WGS-TPSR KW - Zr Y1 - 2021 U6 - https://doi.org/10.1002/er.6646 SN - 1099-114X ER - TY - GEN A1 - Baena-Moreno, Francisco Manuel A1 - González-Castaño, Miriam A1 - Navarro de Miguel, Juan Carlos A1 - Miah, Kamal Uddin Mohammad A1 - Ossenbrink, Ralf A1 - Odriozola, José Antonio A1 - Arellano-García, Harvey T1 - Stepping toward Efficient Microreactors for CO2 Methanation: 3D Printed Gyroid Geometry T2 - ACS Sustainable Chemistry & Engineering N2 - 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. KW - CO2 methanation KW - gyroid geometry KW - CH4 selectivity KW - gyroid-3D complex Y1 - 2021 U6 - https://doi.org/10.1021/acssuschemeng.1c01980 SN - 2168-0485 VL - 9 IS - 24 SP - 8198 EP - 8206 ER - TY - GEN A1 - González-Castaño, Miriam A1 - Navarro de Miguel, Juan Carlos A1 - Pernkova, A. A1 - Centeno, Miguel Angel A1 - Odriozola, José Antonio A1 - Arellano-García, Harvey T1 - Ni/YMnO3 perovskite catalyst for CO2 methanation T2 - Applied Materials Today N2 - Ni/YMnO3 perovskite catalyst for CO2 methanation KW - Ni catalysts KW - CO2 methanation KW - YMnO3 perovskites KW - manganites Y1 - 2021 U6 - https://doi.org/10.1016/j.apmt.2021.101055 VL - 23 ER - TY - GEN A1 - Mahmood, Safdar A1 - González-Castaño, Miriam A1 - Penkova, Anna A1 - Centeno, Miguel Angel A1 - Odriozola, José Antonio A1 - Arellano-García, Harvey T1 - CO2 methanation on Ni/YMn1-xAlxO3 perovskite catalysts T2 - Applied Materials Today N2 - 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. KW - CO2 methanation KW - Perovskites KW - Ni catalyst KW - Manganese KW - Aluminium Y1 - 2022 U6 - https://doi.org/10.1016/j.apmt.2022.101577 SN - 2352-9407 VL - 29 SP - 1 EP - 11 ER - TY - GEN A1 - González-Castaño, Miriam A1 - Baena-Moreno, Francisco Manuel A1 - Navarro de Miguel, Juan Carlos A1 - Miah, Kamal Uddin Mohammad A1 - Arroyo-Torralvo, Fátima A1 - Ossenbrink, Ralf A1 - Odriozola, José Antonio A1 - Benzinger, Walther A1 - Hensel, Andreas A1 - Wenka, Achim A1 - Arellano-García, Harvey T1 - 3D-printed structured catalysts for CO2 methanation reaction: Advancing of gyroid-based geometries T2 - Energy Conversion and Management N2 - 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 %. KW - 3D-printing KW - Triply periodic minimal surfaces KW - Fluid guiding elements KW - CO2 methanation KW - Structured catalysts KW - Experiment design Y1 - 2022 U6 - https://doi.org/10.1016/j.enconman.2022.115464 SN - 2590-1745 VL - 258 ER - TY - GEN A1 - Bobadilla, Luis F. A1 - Azancot, Lola A1 - Luque-Alvarez, Ligia A. A1 - Torres-Sempere, Guillermo A1 - Gonzalez-Castano, Miriam A1 - Pastor-Perez, Laura A1 - Yu, Jie A1 - Ramirez Reina, Tomas A1 - Ivanova, Svetlana A1 - Centeno, Miguel Angel A1 - Odriozola, José Antonio T1 - Development of Power-to-X Catalytic Processes for CO2 Valorisation: From the Molecular Level to the Reactor Architecture T2 - Chemistry N2 - Nowadays, global climate change is likely the most compelling problem mankind is facing. In this scenario, decarbonisation of the chemical industry is one of the global challenges that the scientific community needs to address in the immediate future. Catalysis and catalytic processes are called to play a decisive role in the transition to a more sustainable and low-carbon future. This critical review analyses the unique advantages of structured reactors (isothermicity, a wide range of residence times availability, complex geometries) with the multifunctional design of efficient catalysts to synthesise chemicals using CO2 and renewable H2 in a Power-to-X (PTX) strategy. Fine-chemistry synthetic methods and advanced in situ/operando techniques are essential to elucidate the changes of the catalysts during the studied reaction, thus gathering fundamental information about the active species and reaction mechanisms. Such information becomes crucial to refine the catalyst’s formulation and boost the reaction’s performance. On the other hand, reactors architecture allows flow pattern and temperature control, the management of strong thermal effects and the incorporation of specifically designed materials as catalytically active phases are expected to significantly contribute to the advance in the valorisation of CO2 in the form of high added-value products. From a general perspective, this paper aims to update the state of the art in Carbon Capture and Utilisation (CCU) and PTX concepts with emphasis on processes involving the transformation of CO2 into targeted fuels and platform chemicals, combining innovation from the point of view of both structured reactor design and multifunctional catalysts development. Y1 - 2022 UR - https://www.mdpi.com/2624-8549/4/4/83 U6 - https://doi.org/10.3390/chemistry4040083 SN - 2624-8549 VL - 4 IS - 4 SP - 1250 EP - 1280 ER -