1998
DOI: 10.1006/jcat.1998.2259
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Effect of Potassium Promotion on Iron-Based Catalysts for Fischer–Tropsch Synthesis

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Cited by 132 publications
(68 citation statements)
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“…1.13). The inhibition effect on the methane formation and the promotion effect of chain growth of potassium are in agreement with the results obtained in several earlier studies on Fe-based catalysts [16,19]. The decrease in methane selectivity and the increase in C 5+ selectivity are due to the increased CO and lower hydrogen surface coverage in the presence of potassium, as discussed before.…”
Section: Effects Of Potassium On Water-gas Shift Reactionsupporting
confidence: 81%
“…1.13). The inhibition effect on the methane formation and the promotion effect of chain growth of potassium are in agreement with the results obtained in several earlier studies on Fe-based catalysts [16,19]. The decrease in methane selectivity and the increase in C 5+ selectivity are due to the increased CO and lower hydrogen surface coverage in the presence of potassium, as discussed before.…”
Section: Effects Of Potassium On Water-gas Shift Reactionsupporting
confidence: 81%
“…The Fe@C catalysts were tested in the FTS reaction at 613 K, 20 bar, H 2 /CO ¼ 1 and gas hourly space velocity (GHSV) of 30,000 h À 1 (space velocity based on catalyst bed volume). Owing to the outstanding effect of potassium promotion on iron-based catalyst for FTS, namely improving activity and olefins to paraffins ratio [33][34][35] , a series of alkali-promoted samples were are also synthesized.…”
Section: Synthesis and Characterizationmentioning
confidence: 99%
“…It shows that although CO addition can be used 2 to decrease CO yields during FTS, the elimination of net CO formation may well 2 2 require levels of CO that are impractical because of separation and re-compression Figure 11 shows CO conversion as a function of reciprocal space velocity under different conditions. Water-gas shift reactions during FT synthesis lead to a reduced water concentration and an increased hydrogen concentration, both of which increase CO conversion rate [19]. Therefore, CO reaction rate was almost independent of space times at 220 C and 235 C. Low temperatures favored the formation of high molecular weight hydrocarbon.…”
Section: +mentioning
confidence: 82%