Fischer-Tropsch Synthesis: Effect of Water Over Iron-Based Catalysts

• Published in: Catalysis letters Vol. 140; no. 3-4; pp. 98 - 105
• Main Authors: Pendyala, Venkat Ramana Rao, Jacobs, Gary, Mohandas, Janet C, Luo, Mingsheng, Hamdeh, Hussein H, Ji, Yaying, Ribeiro, Mauro C, Davis, Burtron H
• Format: Journal Article
• Language: English
• Published: Boston Boston : Springer US 01-12-2010; Springer US; Springer; Springer Nature B.V
• Subjects: Analysis; Catalysis; Catalysts; Chemical synthesis; Chemistry; Chemistry and Materials Science; Continuously stirred tank reactors; Conversion; Deactivation; Effect of temperature; Equivalence; Exact sciences and technology; Fischer-Tropsch process; Fischer-Tropsch synthesis; General and physical chemistry; High temperature; Industrial Chemistry/Chemical Engineering; Iron; Iron carbides; Iron catalyst; Iron oxides; Mössbauer; Organometallic Chemistry; Oxidation; Partial pressure; Physical Chemistry; Potassium; Rare gases; Spectroscopic analysis; Temperature; Theory of reactions, general kinetics. Catalysis. Nomenclature, chemical documentation, computer chemistry; Water effect; X ray absorption; XANES; Water effect; Mössbauer; Iron catalyst; XANES; Effect of temperature; Fischer–Tropsch synthesis; Water; Binary compound; XANES spectrometry; Support; Iron; High temperature; Iron carbide; Stirred tank reactor; Chemical reduction; Magnetite; Oxidation; Low temperature; Deactivation; Transition element compounds; Fischer Tropsch synthesis; Transition metal; Conversion; Velocity; Inert gas; Heterogeneous catalysis; Fischer-Tropsch synthesis; Partial pressure; Potassium; Catalyst
• ISSN: 1011-372X; 1572-879X
• DOI: 10.1007/s10562-010-0452-7

The effect of water on the performance of potassium-promoted precipitated iron catalyst was investigated during Fischer-Tropsch synthesis (FTS) using a continuously stirred tank reactor (CSTR) at two different reaction temperatures. Water was added in such a manner as to replace an equivalent amount of inert gas so that all other reaction conditions (e.g., reactant partial pressure, space velocity) remained the same before, during, and after water addition. The externally added water had a positive effect on CO conversion at 270 °C whereas, for the reaction carried out at 230 °C, the added water decreased CO conversion and deactivated the catalyst. From these findings, the addition of water at 230 °C oxidized the catalyst, transforming the iron carbide to the Fe₃O₄ phase. When the reaction was carried out at 270 °C, severe oxidization did not take place and a carbide phase was retained. The loss in activity and the rate of deactivation were more pronounced at 230 °C compared to the 270 °C condition for the same catalyst. Mössbauer spectroscopic measurements revealed that for the reaction carried out at 230 °C, the catalyst had 85% of the iron present as Fe₃O₄ and the remaining as Hägg carbide (χ-Fe₅C₂), whereas at the higher temperature reaction condition the catalyst had about 66% of the iron present as έ-Fe₂.₂C, with the remaining as Fe₃O₄. These findings were also supported by XANES analysis, where a high white line intensity was observed for the sealed used catalyst sample for the low temperature reaction condition, indicating a higher extent of oxidation. A low white line intensity was recorded for the used sample for the high temperature reaction condition, indicative of a higher extent of reduction. Graphical Abstract The effect of water on the performance of potassium-promoted precipitated iron catalyst was investigated during Fischer-Tropsch synthesis (FTS) by using a continuously stirred tank reactor (CSTR) at two different reaction temperatures. In these studies, the added water replaced an equivalent amount of inert gas so that all other reaction conditions remained the same before, during, and after water addition. The externally added water had a positive effect on CO conversion at 270 °C whereas, for the reaction carried out at 230 °C, the added water decreased CO conversion and deactivated the catalyst. From these findings, the addition of water at 230 °C oxidized the catalyst, completely transforming the iron carbide to the Fe₃O₄ phase. When the reaction was carried out at 270 °C, oxidization did not take place and the carbide phase was retained. The loss in activity and the rate of deactivation were more pronounced at 230 °C compared to the 270 °C condition for the same catalyst. Mössbauer spectroscopic measurements and X-ray absorption near edge spectroscopy (XANES) studies further supported these findings. [graphic removed]