Structural Screening and Design of Dendritic Micro-Mesoporous Composites for Efficient Hydrodesulfurization of Dibenzothiophene and 4,6-Dimethyldibenzothiophene
Alabsi, Mohnnad H.
KAUST DepartmentChemical Science Program
Homogeneous Catalysis Laboratory (HCL)
KAUST Catalysis Center (KCC)
Physical Science and Engineering (PSE) Division
Online Publication Date2020-08-11
Print Publication Date2020-09-09
Embargo End Date2021-08-11
Permanent link to this recordhttp://hdl.handle.net/10754/664620
MetadataShow full item record
AbstractNovel dendritic micro-mesoporous TS-1/dendritic mesoporous silica nanoparticles (DMSNs) composites (TD) were assembled by TS-1 nanocrystals with ultrasmall particle size and strong acidity. TS-1 seeds and DMSNs were composited via the Ti-O-Si chemical bond, which stimulate on the generation of Brønsted (B) and Lewis (L) acid. The spillover d-electrons produced by The Ti element of TS-1 seeds produced a spillover of d-electrons, which could interact with the surface of MoS2 phases, thereby reducing Mo-S interactions and creat sulfur vacancies that are favorable for dibenzothiophene (DBT) and 4,6-dimethyldibenzothiophene (4,6-DMDBT) hydrodesulfurization (HDS) reactions. The increased B&L acid amount of NiMo/TD-2.0 with Cetyltrimethylammonium bromide/Sodium salicylate molar ratio of 2.0 played a important role in facilitating the hydrogenation (HYD) route of DBT HDS and the isomerization (ISO) route of 4,6-DMDBT HDS, which is more favorable to the reduction of steric hindrance of DBT and 4,6-DMDBT reactants in the HDS reaction process. The NiMo/TD-2.0 catalyst exhibited the highest turn-over frequency (TOF) value and HDS reaction rate constant (kHDS) of DBT and 4,6-DMDBT due to its ultrasmall particle size, uniform spherical dendritic morphology, strong B&L acidities and good stacking degree.
CitationWang, X., Xiao, C., Mei, J., Alabsi, M. H., Shi, Y., Zhao, Z., … Xu, C. (2020). Structural Screening and Design of Dendritic Micro-Mesoporous Composites for Efficient Hydrodesulfurization of Dibenzothiophene and 4,6-Dimethyldibenzothiophene. ACS Applied Materials & Interfaces. doi:10.1021/acsami.0c12631
SponsorsThis work was financially supported by National Natural Science Foundation of China (No. 21878330 and 21808079), CNPC Key Research Project (2016E-0707), Key Research and Development Program of Shandong Province (No.2019GSF109115), and the King Abdullah University of Science and Technology (KAUST) Office of Sponsored Research (OSR) under Award (No. OSR-2019-CPF 4103.2).
PublisherAmerican Chemical Society (ACS)