Self-optimising chemical systems have experienced a growing momentum in recent years. Herein, we review algorithms used for the self-optimisation of chemical reactions in an accessible way for the general chemist.
A universal multistage cascade CSTR
has been developed that is
suitable for a wide range of continuous-flow processes. Coined by
our group the “Freactor” (free-to-access reactor), the
new reactor integrates the efficiency of pipe-flow processing with
the advanced mixing of a CSTR, delivering a general “plug-and-play”
reactor platform which is well-suited to multiphasic continuous-flow
chemistry. Importantly, the reactor geometry is easily customized
to accommodate reactions requiring long residence times (≥3
h tested).
Progress reaction profiles are affected by both catalyst activation and deactivation processes occurring alongside the main reaction. These processes complicate the kinetic analysis of reactions, often directing researchers toward incorrect conclusions. We report the application of two kinetic treatments, based on variable time normalization analysis, to reactions involving catalyst activation and deactivation processes. The first kinetic treatment allows the removal of induction periods or the effect of rate perturbations associated with catalyst deactivation from kinetic profiles when the quantity of active catalyst can be measured. The second treatment allows the estimation of the activation or deactivation profile of the catalyst when the order of the reactants for the main reaction is known. Both treatments facilitate kinetic analysis of reactions suffering catalyst activation or deactivation processes.
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