TY - JOUR
T1 - Fischer–Tropsch Synthesis
T2 - XANES Spectra of Potassium in Promoted Precipitated Iron Catalysts as a Function of Time On-stream
AU - Jacobs, Gary
AU - Pendyala, Venkat Ramana Rao
AU - Martinelli, Michela
AU - Shafer, Wilson D.
AU - Gnanamani, Muthu Kumaran
AU - Khalid, Syed
AU - MacLennan, Aimee
AU - Hu, Yongfeng
AU - Davis, Burtron H.
N1 - Publisher Copyright:
© 2017, Springer Science+Business Media New York.
PY - 2017/8
Y1 - 2017/8
N2 - XANES K-edge spectra of potassium promoter in precipitated Fe catalysts were acquired following activation by carburization in CO and as a function of time on-stream during the course of a Fischer–Tropsch synthesis run for a 100Fe:2K catalyst by withdrawing catalysts, sealed in wax product, for analysis. CO-activated and end-of-run spectra of the catalyst were also obtained for a 100Fe:5K catalyst. Peaks representing electronic transitions and multiple scattering were observed and resembled reference spectra for potassium carbonate or potassium formate. The shift in the multiple scattering peak to higher energy was consistent with sintering of potassium promoter during the course of the reaction test. The catalyst, however, retained its carbidic state, as demonstrated by XANES and EXAFS spectra at the iron K-edge, suggesting that sintering of potassium did not adversely affect the carburization rate, which is important for preventing iron carbides from oxidizing. The method serves a starting point for developing better understanding of the chemical state and changes in structure occurring with alkali promoter. Graphical Abstract: [Figure not available: see fulltext.].
AB - XANES K-edge spectra of potassium promoter in precipitated Fe catalysts were acquired following activation by carburization in CO and as a function of time on-stream during the course of a Fischer–Tropsch synthesis run for a 100Fe:2K catalyst by withdrawing catalysts, sealed in wax product, for analysis. CO-activated and end-of-run spectra of the catalyst were also obtained for a 100Fe:5K catalyst. Peaks representing electronic transitions and multiple scattering were observed and resembled reference spectra for potassium carbonate or potassium formate. The shift in the multiple scattering peak to higher energy was consistent with sintering of potassium promoter during the course of the reaction test. The catalyst, however, retained its carbidic state, as demonstrated by XANES and EXAFS spectra at the iron K-edge, suggesting that sintering of potassium did not adversely affect the carburization rate, which is important for preventing iron carbides from oxidizing. The method serves a starting point for developing better understanding of the chemical state and changes in structure occurring with alkali promoter. Graphical Abstract: [Figure not available: see fulltext.].
KW - Fischer–Tropsch synthesis
KW - Iron-based catalyst
KW - Olefin selectivity
KW - Potassium promoter
KW - XANES/EXAFS
UR - http://www.scopus.com/inward/record.url?scp=85020284759&partnerID=8YFLogxK
UR - http://www.scopus.com/inward/citedby.url?scp=85020284759&partnerID=8YFLogxK
U2 - 10.1007/s10562-017-2090-9
DO - 10.1007/s10562-017-2090-9
M3 - Article
AN - SCOPUS:85020284759
SN - 1011-372X
VL - 147
SP - 1861
EP - 1870
JO - Catalysis Letters
JF - Catalysis Letters
IS - 8
ER -