Adsorption of mercaptobenzoheterocyclic compounds on sulfide mineral surfaces: A density functional theory study of structure–reactivity relations

Abstract

Mercaptobenzoheterocyclic compounds: 2-mercaptobenzothiazole (MBT), 2-mercaptobenzoxazole (MBO) and 2-mercaptobenzimidazole (MBI) are widely used as corrosion inhibitors and flotation collectors, but the true nature of the adsorption selectivity and activity to solid surfaces is still unclear. Using density functional theory (DFT) calculations, this study investigates the structure–reactivity relation of MBO, MBI and MBT as flotation collectors with sulfide minerals. The results demonstrate that the O, N and S heteratoms in MBO, MBI and MBT molecules can attend the chemical bond formation with metal atoms on mineral surfaces and significantly impact the chemical reactivity of these mercaptobenzoheterocyclic compounds, and the reactive power of the three compounds to metal and mineral surfaces is predicted to be MBT>MBI≥MBO. In addition, the chemical reactivity of the thione, thiol and ionized thiol species of these mercaptobenzoheterocyclic compounds in both vacuum and aqueous phases is also studied. The results show that the thione tautomers of MBO, MBI and MBT is more stable and reactive than their thiol tautomers, and in aqueous solutions, the ionized thiol exhibits the strongest reactivity. The theoretical results of structure–reactivity relations provide an atomic level understanding of the activity and selectivity observed by the experimental investigation of the adsorption of MBO, MBI and MBT on metal and sulfide surfaces. The further pyrite flotation tests indicate that MBT has the highest collecting power to pyrite, followed by MBI and then MBO, which is consistent with the theoretical prediction.