Linear α-olefins (LAOs) from CO/H2 represent an attractive non-petroleum route, yet their selective formation over Fe catalysts is often limited by CO2 formation via water–gas shift (WGS) reaction and by secondary hydrogenation that consumes terminal olefins. In this work, we demonstrate that these competing pathways can be regulated on carbon-nanotube (CNT) supported Fe catalysts by controlling the CNT interfacial oxygen environment through NO treatment or high-temperature annealing and by adjusting the Mn incorporation protocol between co-impregnation and stepwise addition. Under identical reaction conditions at 280 °C and 3.0 MPa with an H2-to-CO ratio of 1, high-temperature treated CNTs improve olefin preservation and LAO retention compared with NO-treated CNTs. Mn promotion further shifts selectivity toward α-olefins and lowers CO2 selectivity. At the same Fe-to-Mn ratio, the Mn introduction sequence produces distinct reducibility and CO-binding behaviors that lead to different steady-state oxide and carbide phases. XPS, H2-TPR, and CO-TPD collectively suggest that CNT pretreatment and the Mn protocol modulate near-surface oxygen speciation, reduction kinetics, and CO adsorption strength. Mössbauer spectroscopy confirms a predominantly χ-Fe5C2 population and indicates the presence of ε-Fe2C in selected samples together with residual oxide and superparamagnetic Fe species. These results highlight the importance of controlling the CNT–metal interface and Mn–Fe proximity to enhance LAO retention under high-temperature CO hydrogenation.
Zhang et al. (Thu,) studied this question.