The development of spatiotemporal complexity in a chemical reaction in a 'C
ouette reactor' is analysed through the Lengyel-Epstein model for the chlor
ine dioxide-iodine-malonic acid (CDIMA) reaction which is characteristic of
a system showing instability through supercritical Hopf bifurcation (as op
posed to excitable systems). The Couette reactor comprises the annular gap
between two concentric cylinders, the inner of which is rotated at a contro
lled rate so as to establish Taylor-Couette flow, which dominates the trans
port of molecules along the reactor. The 'boundary conditions' for the Coue
tte reactor are set by well-stirred continuous flow reactors (CSTRs), which
may be operated with different chemical inputs, so imposing background rea
ctant concentrations along the Couette reactor. We examine this system anal
ytically and numerically using a simplified representation of the Taylor-Co
uette flow through an 'enhanced' reaction-diffusion model and restrict ours
elves at this stage to operating conditions such that the steady states in
the CSTRs are stable rather than oscillatory. Despite this, and the stabili
sing effects of the boundary conditions thus imposed, complex spatiotempora
l responses develop within the Couette reactor for a range of parameter val
ues. We determine the variation in stability of the (spatially-dependent) s
teady state concentration profiles and observe both saddle-node and Hopf bi
furcations. The unsteady solutions that emerge from the Hopf bifurcations s
how subsequent instabilities, possibly through a period-doubling-mixed-mode
sequence to more complex structures.