Structured catalysts based on open-cell metallic foams coated by a catalytic film offer a great potential for intensification and optimization of catalytic processes. Here, we demonstrated the feasibility of the electrodeposition to synthesize in situ and quick Rh/Mg/Al hydrotalcite-type (HT) syngas catalyst precursors with controlled composition, morphology and thickness around 5 to 20 mu m on the surface of FeCrAlloy foams using a two-compartment flow electrochemical cell. After calcination at 900 degrees C, catalytic coatings with properties similar to those of conventional co-precipitated HT-derived catalysts were identified by synchrotron nano-XRF/XRD tomography and HRTEM. The resulting structured catalysts, therefore, merged the properties of both HT-derived catalysts and open-cell foams, namely, thermally stable nano MgO- and spinel-type phases where Rh was dispersed and stabilized against sintering, and high mass and heat transfer. Moreover, the development of a MgAl2O4 thin film in the support-coating interface, by chemical reaction between Mg2+ from the coating and Al3+ from the support during calcination, increased the catalyst adhesion. Consequently, active and stable performance was obtained under harsh reaction conditions in the catalytic partial oxidation of CH4 to syngas as a model reaction. Even in the catalysts operating under severe reaction conditions for about 50 h, the coating was stable and Rh metallic nanoparticles around 2 nm were still well dispersed.

Coprecipitated-like hydrotalcite-derived coatings on open-cell metallic foams by electrodeposition: Rh nanoparticles on oxide layers stable under harsh reaction conditions

Gondolini Angela;
2018

Abstract

Structured catalysts based on open-cell metallic foams coated by a catalytic film offer a great potential for intensification and optimization of catalytic processes. Here, we demonstrated the feasibility of the electrodeposition to synthesize in situ and quick Rh/Mg/Al hydrotalcite-type (HT) syngas catalyst precursors with controlled composition, morphology and thickness around 5 to 20 mu m on the surface of FeCrAlloy foams using a two-compartment flow electrochemical cell. After calcination at 900 degrees C, catalytic coatings with properties similar to those of conventional co-precipitated HT-derived catalysts were identified by synchrotron nano-XRF/XRD tomography and HRTEM. The resulting structured catalysts, therefore, merged the properties of both HT-derived catalysts and open-cell foams, namely, thermally stable nano MgO- and spinel-type phases where Rh was dispersed and stabilized against sintering, and high mass and heat transfer. Moreover, the development of a MgAl2O4 thin film in the support-coating interface, by chemical reaction between Mg2+ from the coating and Al3+ from the support during calcination, increased the catalyst adhesion. Consequently, active and stable performance was obtained under harsh reaction conditions in the catalytic partial oxidation of CH4 to syngas as a model reaction. Even in the catalysts operating under severe reaction conditions for about 50 h, the coating was stable and Rh metallic nanoparticles around 2 nm were still well dispersed.
2018
Istituto di Scienza, Tecnologia e Sostenibilità per lo Sviluppo dei Materiali Ceramici - ISSMC (ex ISTEC)
Electrodeposition
Hydrotalcite
FeCrAlloy foam
Structured catalyst
Syngas
rhodium
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Utilizza questo identificativo per citare o creare un link a questo documento: https://hdl.handle.net/20.500.14243/345644
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