Ethylcyclopentane ring opening reaction over PtGe/Al2O3 catalysts prepared by controlled surface reaction |
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| Authors: | Serge Ello Laurence Pirault-Roy Attila Wootsch Zoltán Paál |
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| Affiliation: | (1) Faculté des Sciences, LACCO-UMR 6503 CNRS-Université de Poitiers, 40, Avenue du Recteur Pineau, F-86022 Poitiers Cedex, France;(2) Laboratoire de Chimie-Physique, Université de Cocody 22, BP582, Abidjan, Cote d’Ivoire;(3) Institute of Isotopes, Hungarian Academy of Sciences, P O. Box 77, Budapest, H-1525, Hungary;(4) Present address: Comergen Inc., Záhony u. 7, 1031 Budapest, Hungary |
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| Abstract: | Platinum-germanium catalysts supported on a non-acidic Al2O3 have been prepared by adding Ge in amounts corresponding nominally to 1/8 (PtGe1/8/Al2O3); 1/2 (PtGe1/2/Al2O3); 1 (PtGe1/Al2O3) and 2 (PtGe2/Al2O3) monolayers by controlled surface reaction of Ge(n-C4H9)4 to Pt/Al2O3. These catalysts were characterized by electron microscopy (TEM), FTIR of CO adsorption and H2 chemisorption. The ring opening of ethylcyclopentane (ECP) was studied as a test reaction between 543 and 633 K. PtGe1/8/Al2O3 catalyst produced the most ring opening products (ROP) in the whole temperature range. A good agreement with statistical values of ROP was observed at low temperature, but at higher temperature, the opening became selective, producing mostly heptane. Bimetallic catalysts PtGe1/Al2O3 and PtGe2/Al2O3 led to a nonselective hydrogenolysis, similar to the monometallic platinum catalyst Pt/Al2O3. The catalysts PtGe1/Al2O3 and PtGe2/Al2O3 produced ROP with the lowest selectivity; instead, much aromatics and fragments were formed, in increasing amounts above 600 K. |
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| Keywords: | Ethylcyclopentane ring opening reaction surface reaction |
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