Demonstrates enhanced stability of cobalt catalysts in water-rich conditions, suggesting a novel stabilization approach.
Cobalt catalysts have been widely studied for Fischer-Tropsch synthesis, yet they gradually deactivate under water-rich reaction conditions. Current stabilization strategies rely on complex catalyst compositions or even use noble-metal promoters. Here, we demonstrate that cobalt deactivation can be effectively hindered by physically regulating water diffusion. By physical mixing of a classical Co/SiO2 catalyst with hydrophobic polydivinylbenzene, a microenvironment is created that promotes directional water transport away from the cobalt. As a result, stable Fischer-Tropsch operation is achieved for 1200 hours, maintaining high activity with 88-90% selectivity toward C5+ hydrocarbons, minimal methane and CO2 production. Mechanistic investigations suggest that the combination of hydrophobic polymer could promote directional water removal from the catalyst surface. These findings demonstrate a practical strategy for stabilizing highly water-sensitive catalysts. Cobalt catalysts are widely used for Fischer–Tropsch synthesis but gradually deactivate under water-rich reaction conditions. Here, the authors demonstrate a practical strategy to stabilize these water-sensitive catalysts by regulating water diffusion.
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