Mechanistic
kinetic models have been developed for the CO2 hydrogenation
reaction with the aim to provide insights into the
mechanism followed for the formation of CO, linear alkanes and alkenes
containing up to 20 carbon atoms, and alcohols and acids containing
up to six carbon atoms over an Fe–K/Al2O3 catalyst in a continuous fixed-bed reactor. On the basis of a redox
mechanism for the reverse water-gas shift reaction, an alkyl mechanism
to explain the chain-growth mechanism and the formation of linear
hydrocarbon chains, and a CO insertion mechanism to explain the formation
of oxygenate products, the kinetic rates for the compounds considered
are derived according to the Langmuir–Hinshelwood–Hougen–Watson
method. Two models are proposed: the first one considers the existence
of only one site for the FT step, where all of the products are formed;
the second model is based on the hypothesis that two different active
sites exist, one for the formation of hydrocarbons and the other for
the formation of oxygenates. Mathematical optimization via least-squares
methods allowed estimation of the kinetic parameters for the two models.
The models were validated against the available experimental data.
Globally, both models give good predictions of the experimental data,
with mean average relative residuals <5%. However, the monosite
model shows a better fit of the experimental data and has a lower
statistical error. Nevertheless, it is not able to accurately predict
the formation of oxygenates, giving a value of the chain-growth probability
that is significantly far from the experimental value. An improved
description of oxygenates is provided by the multisite model, but
it has larger confidence intervals and suffers from a high number
of kinetic parameters. This study globally provides a first investigation
of the mechanism of CO2 hydrogenation, including the formation
of hydrocarbons and oxygenates. It has been shown that a complex mechanism
is involved that includes chain-growth via an alkyl mechanism combined
with a CO insertion mechanism to form the oxygenate products.