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Reforming reactions of heptane on platinum crystals at atmospheric pressures

Conference · · 72nd AIChE Annu. Meet. Prepr.; (United States)
OSTI ID:6187589

In dehydrocyclization of n-heptane to toluene studied at 300/sup 0/-340/sup 0/C, 0.66-4 kPa heptane, and 0-100 kPa hydrogen over a flat Pt(111) surface (A) and stepped Pt(s)-(6(111) x (100)) (B) and Pt(s)-(2(111) x (610)) (C) surfaces, the initial activities of the A and B surfaces were almost equal and twice as large as that of the C surface. The stepped surfaces retained full activity for three hours, but the A surface rapidly deactivated. On each surface, deactivation correlated with carbon deposition, but the amounts of carbon deposited on different surfaces after three hours were similar, suggesting a strong effect of the structure and distribution of surface carbon. Both the initial aromatization rate and the carbon deposition and deactivation increased with increasing temperature and heptane pressure and with decreasing hydrogen pressure. Apparently, the narrow terraces of the C surface are inactive, and aromatization occurs at its step sites. On the B surface, both the steps and the wider terraces are active, with the presence of steps stabilizing the activity of the terraces.

Research Organization:
Univ. of California, Berkeley
OSTI ID:
6187589
Report Number(s):
CONF-791108-
Journal Information:
72nd AIChE Annu. Meet. Prepr.; (United States), Journal Name: 72nd AIChE Annu. Meet. Prepr.; (United States) Vol. 23D
Country of Publication:
United States
Language:
English