Rate equation

Physics

Engineering

Order of reaction

Transmission electron microscopy

Physical chemistry

Kinetics

High-resolution transmission electron microscopy

Catalysis

Reaction rate

Organic chemistry

Chemistry

Hydrodesulfurization

Chemical kinetics

Chemical engineering

Sulfur

Quantum mechanics

Reaction mechanism

Flue-gas desulfurization

Mesoporous material

Reaction rate constant

Activation energy

Journal of Catalysis

The intrinsic kinetics of hydrodesulfurization (HDS) of 4,6-dimethyldibenzothiophene (4,6-DMDBT) over mesoporous CoMoS2/ZSM-5 (CoMoS2/MZSM-5) was investigated by comparing the commercial CoMoS2/γ-Al2O3. A pseudo-first-order kinetic model considering the direct desulfurization (DDS) and two detailed partial and full hydrogenation pathways was formulated with simple power law rate equations. The apparent rate constants of five lumped reactions on CoMoS2/MZSM-5 are 2–4 times larger than those of CoMoS2/γ-Al2O3. With both catalyst system, the pre-exponential factor plays a dominant role in the reaction rate of DDS pathway showing equally high activation energies. The apparent activation energies show a critical effect on the reaction rate of two hydrogenation and subsequent desulfurization reactions. Furthermore, the Delplot analysis was applied to identify the reaction sequence of product formation and verify the reaction network. The HDS performance and reaction rates of individual reaction steps can be rationally linked to the morphology and available content of CoMoS phase as identified by HRTEM and XPS characterization. Thus, multi-stacked MoS2 nanocrystallites on CoMoS2/MZSM-5 provide more available sulfur vacancies to facilitate the DDS pathway, and catalyze efficiently the hydrogenation and subsequent desulfurization with the synergy of brim sites and sulfur vacancies.

Insights into the intrinsic kinetics for efficient hydrodesulfurization of 4,6-dimethyldibenzothiophene over mesoporous CoMoS2/ZSM-5