Direct synthesis of liquid fuels and aromatics from syngas over mesoporous FeZrOx catalyst mixed with Mo/ferrierite

• Published in: Fuel (Guildford) 2020-03, Vol.264, p.116851, Article 116851
• Main Authors: Ali, Mansoor, Koo, Hyun-Mo, Kasipandi, Saravanan, Han, Gui Young, Bae, Jong Wook
• Format: Article
• Language: English
• Subjects: Aromatic compounds; Bimetals; BTX; Carbon dioxide; Carbon monoxide; Catalysts; Catalytic activity; Distillates; Ferrozirconium; Fischer-Tropsch process; Fischer-Tropsch synthesis (FTS) reaction; Hybrid catalyst; Hydrophobicity; Iron oxides; Liquid fuels; Middle distillates; Mo-modified ferrierite (Mo/HFER); Optimization; Ordered mesoporous Fe2O3-ZrO2; Oxides; Selectivity; Synergistic effect; Synthesis gas
• ISSN: 0016-2361; 1873-7153
• DOI: 10.1016/j.fuel.2019.116851

[Display omitted] •Middle distillates and aromatics synthesis from syngas was studied on hybrid FeZrOx-Mo/HFER.•FeZr-Mo(6 wt%)/HFER showed synergistic effects with a higher CO conversion to liquid fuels and aromatics.•Optimal hydrophobicity and acidic sites on the Mo/HFER were responsible for an enhanced catalytic stability. Fischer–Tropsch synthesis (FTS) reaction on the hybrid catalysts containing a highly ordered mesoporous FeZrOx bimetal oxide physically mixed with Mo-modified ferrierite (Mo/HFER) were carried out to directly produce environmentally benign middle distillates and aromatics (BTXs) from syngas. Compared to the pristine FeZrOx itself, the simply mixed hybrid catalyst largely enhanced the selectivity to middle distillates and aromatics (BTXs) through direct CO hydrogenation by preserving its original ordered structures in the forms of partially reduced iron oxides due to their stronger interactions. At an optimal Mo content (~6 wt%) on the HFER frameworks, the hybrid FeZr-Mo(6)/HFER showed the synergistic effects such as higher CO conversion (59.7%) to liquid hydrocarbons (78.4% for C5–C20, 3.7% for C21+ and 5.7% for aromatics including BTXs) with a smaller CO2 formation due to the less accumulation of carbonaceous deposits, optimum hydrophilicity, lower water-gas shift (WGS) reaction activity and larger number of weak acid sites. However, an excessive amount of Mo promoter (>6 wt%) on the acidic HFER surfaces accelerated the formation of the graphitic carbons leading to the decrease of catalytic activity, which were attributed to its excess hydrophobicity and small amounts of acidic sites.