Mechanical insight into the formation of H2S from thiophene pyrolysis: The influence of H2O

Abstract

The thermal utilization of waste rubber is accompanied by the release of sulfur, and the release of H2S to the gas phase is one of the crucial issues. In this work, density functional theory (DFT) calculations and wave function analysis were employed to explore the possible formation pathways of H2S and its precursor (·SH radical) during the pyrolysis of thiophene in the presence of H2O. It indicates that H2O affects the decomposition of thiophene and the formation of H2S in two patterns. First, H2O can participate in the hydrogen transfer process by acting as a catalyst or generating weak hydrogen bonds with thiophene. In this way, the hydrogen transfer reactions are promoted with lower energy barriers, and thus the formation of H2S is facilitated by H2O without changing the pyrolysis pathways. Secondly, H2O can saturate the thiophene ring by addition reactions and alter the generation pathways of H2S significantly. The energy barriers can be decreased with one or two CC bonds of thiophene being saturated. The completely saturated thiophene results in a greater decline of the overall energy barriers for H2S formation. H2O provides the H atom for H2S in the second pattern. Due to the combination of the two influence patterns, the release of H2S can be promoted greatly in the presence of H2O. The present study aims to lay a foundation for the clean thermal utilization of thiophene/rubber and to inspire the advance of desulfurization techniques.