摘要
Removal of sulfur species from blast furnace gas is urgently needed due to the strict emission limits imposed on iron-steel industrial flue gas. Improving the sulfur capacity of H 2 S is a crucial challenge to reduce the operation cost. NiFe layered double hydroxide (LDH) adsorbents were synthesized using the hydrothermal method to strengthen the adsorption of H 2 S, achieving a high sulfur capacity of 133.6 mg/g at 50 °C. Characterization studies have revealed that the reaction pathway of H 2 S on the NiFe LDH surface involves adsorption, dissociation and oxidation. It has been clarified that the high sulfur capacity can be attributed to the abundant H 2 S dissociation sites and the excellent O 2 activation sites. The dissociation sites of H 2 S encompass metal sites, -OH and CO 3 2- . The interaction between O 2 and the bridge site of asymmetric metal atoms significantly enhances the dissociation of O 2 . Strengthening the dissociation of H 2 S and O 2 improves the sulfur capacity. The deactivation of adsorbents comes from the continuous consumption of oxygen species mainly composed of -OH and the deposition of sulfur species in the smaller mesopores ranging from 2 to 10 nm. This work provides useful insights into designing highly efficient iron-based adsorbents for the desulfurization of blast furnace gas.
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