Indexed by:Journal Article

First Author:Dong, Chao

Correspondence Author:Li, X (reprint author), Dalian Univ Technol, Sch Chem Engn, Dalian 116024, Peoples R China.

Co-author:Chen, Yongying,Li, Xiang,Wang, Anjie

Date of Publication:2017-11-15

Journal:2nd International Symposium on Catalytic Science and Technology in Sustainable Energy and Environment (EECAT)

Included Journals:CPCI-S、EI、SCIE、Scopus

Document Type:J

Volume:297

Issue:,SI

Page Number:124-130

ISSN:0920-5861

Key Words:Palladium; Platinum; MCM-41; Alkali-metal cation; Hydrodesulfurization; Dibenzothiophene

Summary:Na+ and K+ were introduced to siliceous MCM-41 (Si-MCM-41) by ion-exchange of Si-MCM-41 with sodium oxalate or potassium oxalate, respectively. The supported Pd and Pt catalysts were prepared by an incipient wetness impregnation method. Their hydrodesulfurization (HDS) performances were evaluated using dibenzothiophene as the model molecule. The introduction of Na+ or K+ led to a decrease in the metal dispersions but an increase in the electron densities of metal sites. It also strongly inhibited the adsorption, dissociation, and probably the spillover of H-2 on the catalysts. Independent of the type of metal, a push-pull effect of Na+ and K+ on the HDS performances of the Pd and Pt catalysts was observed. They on the one hand enhanced the direct desulfurization pathway (DDS), but on the other hand hindered the hydrogenation route. The DDS activity of Pt increased almost linearly with its electron density. These are discussed by considering both the negative effects of Na+ and K+ on the formation of active hydrogen species and their positive role on the electron densities of the metal sites. The Pt catalysts deactivated faster than the Pd catalysts. The kinetic study indicates that Na+ and K+ did not affect the deactivation of the catalysts.