Thermochemistry of Catalyst Deactivation II: Competition between Hydrogenation, Condensation and Hydrocracking
Paul R. Robinson, Chevron Lummus Global, 100 Chevron Way, 10-3210, Richmond, CA 94801

 

The first paper in this series presented the results of equilibrium calculations for the competition between the hydrogenation of naphthalene to form tetralin and decalin (Reactions 1-2) and the condensation of naphthalene with o-xylene to form chrysene (Reaction 3). This set of reactions was proposed as a simple model for the coke-induced deactivation of hydrotreating catalysts.

Saturation (Reversible)

1. Naphthalene (C10H8) + 2H2  ↔  Tetralin (C10H12)

2. Tetralin + 3H2  ↔  Decalin (C10H18)

Condensation (Irreversible)

3. Naphthalene + o-Xylene  →  Chrysene (C18H12) + 3H2

4. Chrysene  → → →  Coke + xH2

This paper shows the effect of adding a hydrocracking reaction (Reaction 5).

Hydrocracking (Irreversible)

5. Tetralin + H2  →  1-propyl-2-methyl benzene (C10H14)

In addition, for all reactions the thermochemical effects of hydrogen purity at constant total pressure are computed, along with the effects of excess hydrogen, i.e., “gas-to-oil ratio.”

Extended Abstract Status: Not Uploaded

Advances in Hydroprocessing - I

The Preliminary Program for 2007 Spring National Meeting