2020
DOI: 10.1016/j.apcata.2020.117840
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Diffusion-dependent upgrading of hydrocarbons synthesized by Co/zeolite bifunctional Fischer–Tropsch catalysts

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Cited by 13 publications
(2 citation statements)
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“…This was the same as the path reported in the literature. 47,48 According to the reaction energy barriers and reaction heat of R4, R5, and R6, it can be seen that the reaction energy barrier of R5 was 1.05 eV, lower than that of R4. Therefore, the optimal reaction path of H-assisted in the CO dissociation process was: CO hydrogenated to HCO first, then hydrogenated to H 2 CO, and finally H 2 CO dissociated to the CH 2 species (R1 -R5 -R6 path).…”
Section: H-assisted Co Dissociationmentioning
confidence: 99%
“…This was the same as the path reported in the literature. 47,48 According to the reaction energy barriers and reaction heat of R4, R5, and R6, it can be seen that the reaction energy barrier of R5 was 1.05 eV, lower than that of R4. Therefore, the optimal reaction path of H-assisted in the CO dissociation process was: CO hydrogenated to HCO first, then hydrogenated to H 2 CO, and finally H 2 CO dissociated to the CH 2 species (R1 -R5 -R6 path).…”
Section: H-assisted Co Dissociationmentioning
confidence: 99%
“…The implementation of such technologies involves the creation of multifunctional catalytic systems that are effective in the conditions of FT synthesis and that have potential in the reactions of hydrocracking, isomerization, oligomerization, aromatization and hydrogenation of hydrocarbons [7][8][9][10][11][12][13][14][15][16]. The catalyst simultaneously implements the function of FT synthesis (hydrogenating metals) and hydrorefining products (zeolites or zeolitelike structures).…”
Section: Introductionmentioning
confidence: 99%