High-temperature Fischer–Tropsch synthesis over the Li-promoted FeMnMgOx catalysts. (1st July 2022)
- Record Type:
- Journal Article
- Title:
- High-temperature Fischer–Tropsch synthesis over the Li-promoted FeMnMgOx catalysts. (1st July 2022)
- Main Title:
- High-temperature Fischer–Tropsch synthesis over the Li-promoted FeMnMgOx catalysts
- Authors:
- Ma, Zhunzhun
Qian, Weixin
Zhang, Haitao
Ma, Hongfang
Sun, Qiwen
Ying, Weiyong - Abstract:
- Graphical abstract: Highlights: Mg facilitated dissociative CO adsorption and hydrogen adsorption. Mg suppressed the carbonization and weakened the chain propagation. ε'-Fe2.2 C revealed better C–C coupling and higher FTS activity than χ-Fe5 C2 . Li facilitated the formation of the ε'-Fe2.2 C and inhibited the formation of CH4 . FeMnMg-0.75Li had the highest space time yield of light olefins at 355 g/(kg Cat ·h). Abstract: Fischer–Tropsch-to-Olefins (FTO) over iron-based catalysts is a promising process for the production of light olefins from a non-petroleum source. However, the catalytic mechanism is unclear because of the variation in the iron phase during the reduction and activation processes and the complex iron phase composition under the reaction conditions. A series of Li-promoted FeMnMgOx catalysts is synthesized using co-precipitation and impregnation methods, after which the effect of promoters on the evolution of the iron phase, chemisorption, and FTO performance are analyzed. The results demonstrate that Mg enhances dissociative CO adsorption and hydrogen adsorption, improving the FTO activity. Mg facilitates the dispersion of α-Fe2 O3 and suppresses the carbonization, which weakens the chain propagation, encourages the formation of short-chain hydrocarbons, and increases the selectivity of light olefins. Li also enhances dissociative CO adsorption and increases CO conversion. Moreover, Li facilitates the formation of the ε'-Fe2.2 C phase, which reveals aGraphical abstract: Highlights: Mg facilitated dissociative CO adsorption and hydrogen adsorption. Mg suppressed the carbonization and weakened the chain propagation. ε'-Fe2.2 C revealed better C–C coupling and higher FTS activity than χ-Fe5 C2 . Li facilitated the formation of the ε'-Fe2.2 C and inhibited the formation of CH4 . FeMnMg-0.75Li had the highest space time yield of light olefins at 355 g/(kg Cat ·h). Abstract: Fischer–Tropsch-to-Olefins (FTO) over iron-based catalysts is a promising process for the production of light olefins from a non-petroleum source. However, the catalytic mechanism is unclear because of the variation in the iron phase during the reduction and activation processes and the complex iron phase composition under the reaction conditions. A series of Li-promoted FeMnMgOx catalysts is synthesized using co-precipitation and impregnation methods, after which the effect of promoters on the evolution of the iron phase, chemisorption, and FTO performance are analyzed. The results demonstrate that Mg enhances dissociative CO adsorption and hydrogen adsorption, improving the FTO activity. Mg facilitates the dispersion of α-Fe2 O3 and suppresses the carbonization, which weakens the chain propagation, encourages the formation of short-chain hydrocarbons, and increases the selectivity of light olefins. Li also enhances dissociative CO adsorption and increases CO conversion. Moreover, Li facilitates the formation of the ε'-Fe2.2 C phase, which reveals a higher FTS activity and better C–C coupling ability than the χ-Fe5 C2 phase. This results in a decrease in CO2 and increase in light olefins. At the optimal Li loading, the FeMnMg-0.75Li sample displays the highest space time yield of light olefins at 355 g/(kgcat ·h). … (more)
- Is Part Of:
- Fuel. Volume 319(2022)
- Journal:
- Fuel
- Issue:
- Volume 319(2022)
- Issue Display:
- Volume 319, Issue 2022 (2022)
- Year:
- 2022
- Volume:
- 319
- Issue:
- 2022
- Issue Sort Value:
- 2022-0319-2022-0000
- Page Start:
- Page End:
- Publication Date:
- 2022-07-01
- Subjects:
- Fischer–Tropsch synthesis -- Light olefins -- Magnesium -- Lithium -- Iron-based catalyst
Fuel -- Periodicals
Coal -- Periodicals
Coal
Fuel
Periodicals
662.6 - Journal URLs:
- http://www.sciencedirect.com/science/journal/latest/00162361 ↗
http://www.elsevier.com/journals ↗ - DOI:
- 10.1016/j.fuel.2022.123613 ↗
- Languages:
- English
- ISSNs:
- 0016-2361
- Deposit Type:
- Legaldeposit
- View Content:
- Available online (eLD content is only available in our Reading Rooms) ↗
- Physical Locations:
- British Library DSC - 4048.000000
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British Library HMNTS - ELD Digital store - Ingest File:
- 21319.xml