A systematic design method was used to develop a pilot-scale simulated
moving bed (SMB) process for the fractionation of two amino acids, tr
yptophan and phenylalanine. In this method, isotherms were estimated u
sing both frontal chromatography and batch equilibrium methods, and ma
ss-transfer parameters were estimated using frontal chromatography dat
a. SMB experiments were then conducted using the zone flow rates and p
ort velocity calculated from a theoretical analysis without considerin
g mass-transfer effects (an equilibrium design). The estimated paramet
ers were validated with computer simulation and SMB data based on the
equilibrium design. A design considering mass-transfer effects (a none
quilibrium design) was then obtained from the standing wave analysis a
nd tested experimentally. The effluent histories at the extract, raffi
nate, and sampling ports agreed with those from computer simulations.
A sensitivity analysis shows that accurate isotherms, intraparticle di
ffusivities, and bed voidage are important for the SMB design, and the
nonequilibrium design is more robust than the equilibrium design, Var
ious column configurations were compared in terms of throughput and de
sorbent consumption.