English
 
Help Privacy Policy Disclaimer
  Advanced SearchBrowse

Item

ITEM ACTIONSEXPORT

Released

Talk

Characterization of Surface Sites Using IR-Spectroscopy & Microcalorimetry

MPS-Authors
/persons/resource/persons21673

Jentoft,  Friederike C.
Inorganic Chemistry, Fritz Haber Institute, Max Planck Society;

External Resource
No external resources are shared
Fulltext (public)
Supplementary Material (public)
There is no public supplementary material available
Citation

Jentoft, F. C. (2004). Characterization of Surface Sites Using IR-Spectroscopy & Microcalorimetry. Talk presented at Colloquium at UMR CNRS (Ecole Européenne de Chimie, Polymères et Matériaux) - Université Louis Pasteur. Strasbourg, France. 2004-02-18 - 2004-02-18.


Cite as: http://hdl.handle.net/11858/00-001M-0000-0011-0D59-4
Abstract
IR spectroscopy is frequently employed to study surface functionalities of catalysts. Sites that do not give rise to vibrations themselves can be investigated via the adsorption of probe molecules. The best probe molecule may often be the reactant itself. The available equipment at FHI will be presented, and the power of the probe molecule approach will be illustrated by two examples: 1. Catalysts consisting of Pt supported on H-Mordenite are industrially employed for the hydroisomerization of n-pentane. We compared catalysts calcined at different temperatures to each other and with Pt-free Mordenite. CO was employed as a probe for Lewis acid and Pt sites and n-butane was used as a representative of alkane reactant. In a separate experiment that mimicked the IR experimental conditions the adsorption of butane was also followed by microcalorimetry. 2. SiO2-supported Ag is a catalyst for the selective hydrogenation of α, β unsaturated aldehydes to the corresponding unsaturated alcohols. It is not known how and at which sites hydrogen is activated. We have followed the reaction of H2 and D2 with the pure support SiO2 and a 9 wt% Ag containing catalyst at temperatures between 373 and 525 K using IR-spectroscopy. The OH-groups of the silica exchanged with D2 to give OD-groups. The kinetics of this reaction were investigated, as were the kinetics of the back-exchange reaction with H2.