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Martin Makosch

Researcher at ETH Zurich

Publications -  11
Citations -  492

Martin Makosch is an academic researcher from ETH Zurich. The author has contributed to research in topics: Catalysis & Nitrobenzene. The author has an hindex of 10, co-authored 11 publications receiving 440 citations. Previous affiliations of Martin Makosch include École Polytechnique Fédérale de Lausanne.

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Organic Thiol Modified Pt/TiO2 Catalysts to Control Chemoselective Hydrogenation of Substituted Nitroarenes

TL;DR: In this paper, a simple surface modification method for Pt/TiO2 catalysts employing organic thiols for the liquid phase selective hydrogenation of 4-nitrostyrene was presented.
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In situ infrared monitoring of the solid/liquid catalyst interface during the three-phase hydrogenation of nitrobenzene over nanosized Au on TiO2

TL;DR: The three-phase hydrogenation of nitrobenzene catalysed by nanosized gold over titania was investigated in a slurry and the spectroscopic measurements provided new insights into the reaction mechanism and an update of the corresponding kinetics.
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Hydrogenation of Nitrobenzene Over Au/MeOx Catalysts—A Matter of the Support

TL;DR: In this paper, the authors proposed a reaction scheme for the electrochemical hydrogenation of substituted nitrobenzene and its derivates in 1898; however, there is an ongoing debate about the reaction mechanism over heterogeneous catalysts.
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Particle size and support effects in hydrogenation over supported gold catalysts

TL;DR: Particle size and support effects were determined for the hydrogenation of nitrobenzene over gold supported on alumina and titania by kinetic experiments, TEM and in situ high energy resolution fluorescence detected X-ray absorption spectroscopy (HERFD XAS) as mentioned in this paper.
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Oxidation State of Ce in CeO2-Promoted Rh/Al2O3 Catalysts during Methane Steam Reforming: H2O Activation and Alumina Stabilization

TL;DR: In this paper, the cerium oxidation state in ceria-doped Rh/Al2O3 catalysts during the methane steam reforming (MSR) reaction was determined by in situ X-ray absorption spectroscopy and online mass spectrometry at 773 K.