The rate of hydroformylation of 1-octene catalyzed by a water soluble catal
yst is measured in mechanically agitated batch reactor at various stirrer s
peeds and organic phase holdups. The data have been analyzed by coupling re
action kinetics to a pseudo-homogeneous gas-liquid-liquid model based on Hi
gbie's penetration theory which takes into account the presence of the disp
ersed organic phase. A rapid liquid-liquid mass transfer of the reactants i
s assumed leading to an equilibrium between the continuous and the disperse
d phases. The predicted values of the rate are in good agreement with the e
xperimental one. The depletion of the organic substrate in the continuous p
hase is found negligible. (C) 1999 Elsevier Science B.V. All rights reserve
d.