Abstract
Thermal decomposition of n-butylbenzene and n-butylcyclohexane was studied under near-critical and supercritical conditions in relation to future jet fuel thermal stability problems. The reactions of n-butylbenzene and n-butylcyclohexane can be explained by free-radical mechanisms, dominated by side-chain cracking. The major liquid products from n-butylbenzene were styrene and toluene. Toluene was the major product in the far supercritical region while styrene was the dominant product in the low-pressure subcritical region. The main liquid products from n-butylcyclohexane were 1-methylcyclohexene and cyclohexane. The 1-methylcyclohexene was a secondary product which was derived from methylenecyclohexane. This conversion was favored at high pressures. High pressures under supercritical conditions promoted radical addition reactions, leading to the formation of some high-molecular-weight compounds which were not observed under low-pressure conditions. The kinetic data obtained for the thermal decomposition of n-butylbenzene and n-butylcyclohexane are in good agreement with the values reported in the literature.
Original language | English (US) |
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Pages (from-to) | 4591-4600 |
Number of pages | 10 |
Journal | Industrial and Engineering Chemistry Research |
Volume | 37 |
Issue number | 12 |
DOIs | |
State | Published - 1998 |
All Science Journal Classification (ASJC) codes
- General Chemistry
- General Chemical Engineering
- Industrial and Manufacturing Engineering