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Naji, M. |
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Motta, Antonella |
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Aletan, Dirar |
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Mohamed, Tarek |
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Ertürk, Emre |
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Taccardi, Nicola |
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Kononenko, Denys |
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Petrov, R. H. | Madrid |
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Alshaaer, Mazen | Brussels |
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Bih, L. |
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Casati, R. |
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Muller, Hermance |
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Kočí, Jan | Prague |
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Šuljagić, Marija |
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Kalteremidou, Kalliopi-Artemi | Brussels |
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Azam, Siraj |
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Ospanova, Alyiya |
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Blanpain, Bart |
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Ali, M. A. |
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Popa, V. |
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Rančić, M. |
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Ollier, Nadège |
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Azevedo, Nuno Monteiro |
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Landes, Michael |
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Rignanese, Gian-Marco |
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Lazzarini, Andrea
in Cooperation with on an Cooperation-Score of 37%
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Publications (3/3 displayed)
- 2018Time-resolved operando studies of carbon supported Pd nanoparticles under hydrogenation reactions by X-ray diffraction and absorptioncitations
- 2017Core-Shell Structure of Palladium Hydride Nanoparticles Revealed by Combined X-ray Absorption Spectroscopy and X-ray Diffractioncitations
- 2017CO2 Hydrogenation over Pt-Containing UiO-67 Zr-MOFs—The Base Casecitations
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article
CO2 Hydrogenation over Pt-Containing UiO-67 Zr-MOFs—The Base Case
Abstract
CO2 hydrogenation was carried out over Pt-containing UiO-67 Zr-MOFs at T = 220–280 °C and ambient pressure, with H2/CO2 = 0.2–9 and contact times, τ = 0.004–0.01 gcat×min×ml−1. The catalysts were characterized by XRD, N2 adsorption, FESEM, TEM and HRTEM, dissolution-NMR, CO chemisorption, IR spectroscopy and TGA. A positive correlation was observed between the degree of Pt reduction and CO2 conversion. Contact time variation experiments showed that CO is a primary product of reaction, while CH4 is a secondary product. Testing of catalyst crystals with 0.15 and 2.0 micron crystal size, respectively, revealed no influence of diffusion on the reaction rate. Comparison to a conventional Pt/SiO2 catalyst showed very similar activation energy, with Eapp = 50±3 kJ×mol−1. However, the turn-over frequency over Pt/SiO2 was significantly lower, and Pt/SiO2 did not yield methane as product. The Pt-containing UiO-67 Zr-MOF catalyst showed stable activity during 60 hours testing.