Thermal cracking of 1-n-butyldecalin at high pressure (100 bar)

The pyrolysis of 1-n-butyldecalin at high pressure (100 bar) was studied in gold sealed tube reactors at 400 °C. It leads to 4 main chemical families of products in order of predominance: (a) normal alkanes (methane, ethane, propane and n-butane), (b) bicyclics (decalin and 1-methyldecalin), (c) hydroaromatics (tetralin and 5-methyltetralin) and (d) diaramatics (naphthalene and 1-methylnaphthalene). This distribution of products suggests that breaking of side alkyl chain and aromatization reactions should prevail at high pressure and low temperature. Reaction pathways are effectively proposed to account for the formation of main products. Both normal alkanes (except CH₄ and C₂H₆) and bicyclics should mainly come from CC bond breaking reactions on the side alkyl chain of 1-n-butyldecalin. Methane and ethane should come from further decomposition of fuel radicals, including ring opening through beta-scissions given the absence of any C₁₂ and C₁₃ compounds in similar quantities. Both hydroaromatics and diaromatics are secondary products, which result from aromatization reactions of decalin and 1-methyldecalin. In our conditions, 1-n-butyldecalin and n-butylcyclohexane have a similar thermal reactivity. A higher yield in n-butane was observed in the case of 1-n-butyldecalin. In comparison with the pyrolysis of decalin at low pressure (≤1 atm) and high temperature (>500 °C), the production of naphthalene and the absence of any BTX (Benzene, Toluene and Xylene) in detectable quantities is here worth mentioning.

Products Used in this Publication

1-n-Butyldecalin (BD)