Effects of Alumina Phases on the Structural Evolution of Iron Catalysts for the Catalytic Conversion of CO<sub>2</sub> to Olefins
Weifeng Yu, Minghui Zhu, Zixu Yang, Yi‐Fan Han
Abstract
Alumina is extensively used as a catalyst support in a wide range of heterogeneous catalyst systems, where its phase structure significantly influences catalytic properties. Herein, Na-promoted Fe catalysts were impregnated on four different phases of alumina ( γ-, δ -, θ -, and α -Al 2 O 3 ) and evaluated for CO 2 hydrogenation to produce hydrocarbons. Among all the alumina tested, the α-Al 2 O 3 supported Fe catalyst exhibited the best performance, achieving a selectivity of 47.4% for C 2–4 olefins at a CO 2 conversion of 42%, while remaining stable within 200 hour time on stream. As a comparison, the γ-Al 2 O 3 supported Fe catalyst produced mostly CH 4 and CO and deactivates rapidly. In situ characterizations, including Raman, XRD, FTIR, and TPD/TPSR were employed to explore the bulk/surface structural transformation of iron species and elucidate the reaction mechanisms. The distinct differences in catalytic properties are attributed to the variations in surface chemical properties and metal-support interactions, which exert significant influence on CO 2 activation, reduction, carburization, and the generation of FeC X . Notably, γ-Al 2 O 3, with its abundant surface hydroxyl groups, showed weak CO 2 adsorption while strong H 2 adsorption capacity, leading to a more pronounced CH 3 O* signal than α-Al 2 O 3 . This observation suggests an enhanced generation of CH 4 intermediates and a higher hydrogen dissociation capacity, which promotes hydrogenation ability. This study clarifies the impact of the crystalline phases of alumina supports on the structure and composition of iron species and CO 2 hydrogenation activity.