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Kinetic insights into the effect of promoters on Co/Al2O3 for Fischer-Tropsch synthesis

Xiaoli YangCollege of Textiles and Clothing, State Key Laboratory of BioFibers and Eco-textiles, Qingdao University, Qingdao 266071, ChinaJia YangDepartment of Chemical Engineering, Norwegian University of Science and Technology, Trondheim 7491, NorwayTao ZhaoCollege of Textiles and Clothing, State Key Laboratory of BioFibers and Eco-textiles, Qingdao University, Qingdao 266071, ChinaWeixin QianEngineering Research Center of Large Scale Reactor Engineering and Technology, East China University of Science and Technology, Shanghai 200237, ChinaYalan WangDepartment of Chemical Engineering, Norwegian University of Science and Technology, Trondheim 7491, NorwayAnders HolmenDepartment of Chemical Engineering, Norwegian University of Science and Technology, Trondheim 7491, NorwayWei JiangCollege of Textiles and Clothing, State Key Laboratory of BioFibers and Eco-textiles, Qingdao University, Qingdao 266071, ChinaDe ChenDepartment of Chemical Engineering, Norwegian University of Science and Technology, Trondheim 7491, NorwayHaoxi BenCollege of Textiles and Clothing, State Key Laboratory of BioFibers and Eco-textiles, Qingdao University, Qingdao 266071, China
2022en
ABI

Аннотация

The fundamentals of promoter effects in the Fischer − Tropsch synthesis over Co-based catalysts were systematically investigated by employing the Rh, Ir, Sb and Ga as promoters of Co/Al2O3. Various characterizations showed the higher dispersion and reducibility over Rh- and Ir- promoted catalysts would cause a promoted adsorption property, while the Sb- and Ga- promoted catalysts showed a contrary result because the formation of alloy suppressed the accessibility of Co species. Based on the experimental results and kinetic calculations, a linear relationship for the activation energies of these catalysts as a function of activation entropies was proposed. Besides, steady state isotopic transient kinetic analysis (SSITKA) revealed that promoters mainly affected the surface CHx concentration to alter the CO reaction rate, and the chain growth rate constants would affect the product distribution. Since CoRhA and CoIrA greatly enhanced the CHx concentration and inhibited the chain growth ability, they owned a higher CO reaction rate and CH4 selectivity. While the CoSbA and CoGaA suppressed the CHx concentration and intrinsic activity, but enhanced the chain growth ability, thereby revealing a lower CO reaction rate and CH4 selectivity. Furthermore, the reactivity and selectivity difference were attributed to the modification of adsorption strength dictated by the enthalpy of activation on cobalt catalysts with different promoters. These findings provide kinetic insights into the promoter effects and pave the way for optimizing catalysts.

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