High Selectivities to Ethylene by Partial Oxidation of Ethane

Author:

Bodke A. S.1,Olschki D. A.1,Schmidt L. D.1,Ranzi E.2

Affiliation:

1. Department of Chemical Engineering and Materials Science, University of Minnesota, Minneapolis, MN 55455, USA.

2. Departmento di Chemica Industriale e Ingegneria Chemica, Politechnico di Milano, Milan, Italy.

Abstract

At least 85 percent selectivity to ethylene at greater than 70 percent conversion can be obtained by partial oxidation of ethane by adding large amounts of H 2 to the reaction mixture and using a platinum-tin catalyst operating at 950°C with a contact time of ∼10 −3 seconds. This system almost totally shuts off the reactions that form undesired CO and CO 2 , which fall from 20 percent without H 2 to 5 percent when H 2 is added. Although a 2/1 H 2 /O 2 mixture should be explosive at high temperatures, no flames or explosions occur in the presence of ethane. The successive reactions on the catalyst generate more H 2 than used in the feed, so with recycle no additional H 2 would be needed. These results are unexpected because ethylene is a nonequilibrium product and entropy considerations argue that all reaction channels open at high temperatures so the products should approach equilibrium, which predicts only a few percent ethylene. This process is promising for the replacement of steam cracking in the production of ethylene.

Publisher

American Association for the Advancement of Science (AAAS)

Subject

Multidisciplinary

Reference11 articles.

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2. H. H. Kung Transition Metal Oxides: Surface Chemistry and Catalysis (Elsevier New York 1989).

3. Catal. Today 157 (1997); A. Bielanski and J. Haber Oxygen in Catalysis (Dekker New York 1991).

4. Huff M., Schmidt L. D., J. Phys. Chem. 77, 11815 (1993).

5. Yokoyama C., Bharadwaj S. S., Schmidt L. D., Catal. Lett. 38, 181 (1996).

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