Theoretical study of the reaction 2,5-dimethylfuran + H → products

Abstract

The reaction of 2,5-dimethylfuran (DMF) with H-atoms was studied using a potential energy surface calculated at the CBS-QB3 level of theory and master equation/RRKM modeling. Hydrogen abstraction by H-atom and hydrogen additions on DMF were considered. As the decomposition pathways of the initial adducts were unknown, a large number of decomposition routes was explored for these adducts. An important number of interconnected product channels were found and preliminary master equation calculations were performed to select the crucial wells and exit channels. The ipso substitution DMF+H→methylfuran (MF)+CH3 and the formation of 1,3-butadiene and acetyl radical (CH3CO) were found to be the major product channels in the addition process. The total calculated rate constant was found in good agreement with experimental data and is nearly pressure-independent. A small sensitivity to pressure was found for the computed branching ratios. At 1bar, the yields of the two product channels of the addition process are maximal at 1100K with computed branching ratios of 39% (MF+CH3) and 27% (1,3-C4H6+CH3CO). Above 1300K, hydrogen abstraction by H-atom becomes dominant and reaches a branching ratio of 56% at 2000K.