Dibenzyl Disulfide Adsorption on Cationic Exchanged Faujasites: A DFT Study
Etienne Paul Hessou,
Miguel Ponce-Vargas,
Jean-Baptiste Mensah,
Frederik Tielens,
Juan Carlos Santos,
Michael Badawi
Affiliations
Etienne Paul Hessou
Laboratoire de Physique et Chimie Théoriques, Faculté des Sciences et Technologies, CNRS, Université de Lorraine, Boulevard des Aiguillettes, 54500 Vandoeuvre-lès-Nancy, France
Miguel Ponce-Vargas
Institut de Chimie Moléculaire de Reims, Université de Reims Champagne-Ardenne, 51687 Reims, France
Jean-Baptiste Mensah
Laboratoire de Chimie Théorique et de Spectroscopie Moléculaire, Université d’Abomey-Calavi, 03 BP 3409 Cotonou, Benin
Laboratorio de Corrosión, Departamento de Ciencias Químicas, Facultad de Ciencias Exactas, Universidad Andres Bello, Av. República 330, 8370186 Santiago, Chile
Michael Badawi
Laboratoire de Physique et Chimie Théoriques, Faculté des Sciences et Technologies, CNRS, Université de Lorraine, Boulevard des Aiguillettes, 54500 Vandoeuvre-lès-Nancy, France
Although dibenzyl disulfide (DBDS) is used as a mineral oil stabilizer, its presence in electrical transformer oil is associated as one of the major causes of copper corrosion and subsequent formation of copper sulfide. In order to prevent these undesirable processes, MY zeolites (with M = Li, Na, K, Cs, Cu or Ag) are proposed to adsorb molecularly DBDS. In this study, different MY zeolites are investigated at the DFT+D level in order to assess their ability in DBDS adsorption. It was found that CsY, AgY and CuY exhibit the best compromise between high interaction energies and limited S-S bond activation, thus emerging as optimal adsorbents for DBDS.