TY - JOUR
T1 - Variation of residence time with chain length for products in a slurry-phase Fischer-Tropsch reactor
AU - Masuku, Cornelius Mduduzi
AU - Shafer, Wilson Davis
AU - Ma, Wenping
AU - Gnanamani, Muthu Kumaran
AU - Jacobs, Gary
AU - Hildebrandt, Diane
AU - Glasser, David
AU - Davis, Burtron H.
PY - 2012/3
Y1 - 2012/3
N2 - The phrases "product accumulation" or "accumulated products" or "product holdup" have appeared in literature during the past several decades to qualitatively explain the experimental results for Fischer-Tropsch synthesis (FTS). This study develops an experimental method for a slurry reactor to evaluate the product accumulation inside the FT reactor by measuring the average residence time of products as a function of carbon number. The effect of accumulation of products on vapor-liquid equilibrium (VLE) in the reactor is also investigated. The results show that VLE is reached inside the FT reactor for components up to C 17. Furthermore, the relationship between the mole fractions of components in the vapor and the liquid phase for lighter hydrocarbons, up to around C 17, is adequately described by Raoult's law. These results suggests that chain length-dependent solubility in the liquid phase is the predominant cause for chain length dependencies of secondary olefin reactions in FTS, and diffusion-limited removal of products is only significant for products with carbon number greater than 17.
AB - The phrases "product accumulation" or "accumulated products" or "product holdup" have appeared in literature during the past several decades to qualitatively explain the experimental results for Fischer-Tropsch synthesis (FTS). This study develops an experimental method for a slurry reactor to evaluate the product accumulation inside the FT reactor by measuring the average residence time of products as a function of carbon number. The effect of accumulation of products on vapor-liquid equilibrium (VLE) in the reactor is also investigated. The results show that VLE is reached inside the FT reactor for components up to C 17. Furthermore, the relationship between the mole fractions of components in the vapor and the liquid phase for lighter hydrocarbons, up to around C 17, is adequately described by Raoult's law. These results suggests that chain length-dependent solubility in the liquid phase is the predominant cause for chain length dependencies of secondary olefin reactions in FTS, and diffusion-limited removal of products is only significant for products with carbon number greater than 17.
KW - Chain length-related phenomena
KW - Deuterium tracer
KW - Fischer-Tropsch product accumulation
KW - Hydrocarbons residence time
KW - Vapor-liquid equilibrium
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U2 - 10.1016/j.jcat.2011.12.005
DO - 10.1016/j.jcat.2011.12.005
M3 - Article
AN - SCOPUS:84856735413
SN - 0021-9517
VL - 287
SP - 93
EP - 101
JO - Journal of Catalysis
JF - Journal of Catalysis
ER -