M. Diserio et al., KINETIC AND CATALYTIC ASPECTS IN MELT TRANSESTERIFICATION OF DIMETHYLTEREPHTHALATE WITH ETHYLENE-GLYCOL IN THE PRESENCE OF DIFFERENT CATALYTIC-SYSTEMS, Journal of applied polymer science, 62(2), 1996, pp. 409-415
The kinetics of transesterification of dimethyl terephthalate with eth
ylene glycol performed in the presence of catalysts such as: Pb, Zn, M
g, Co, and Mn acetates and a mixture of Mg, Mn, and Zn acetates has be
en studied in semibatch conditions. The catalytic behavior of Sb2O3 ha
s been proven, too. The performance of the different catalytic systems
has been investigated following both the amount of methanol released
during time and the evolution with time of the concentration of any ki
nd of oligomer formed as consequence of the reaction. The oligomers ob
tained were separated, identified, and quantitatively determined by HP
LC analysis. In this way, information have been achieved on both the a
ctivities and selectivities of the different catalysts. The experiment
al data have been interpreted through a classic kinetic model based on
a complex reaction scheme. Despite the complexity of the model, only
two kinetic parameters and two equilibrium constants are necessary to
simulate the kinetic behavior of all the oligomers. A kinetic constant
(K-1) is related to the reaction of a methyl group with a hydroxyl of
ethylene glycol, while the other (K-2) corresponds to the reaction of
a methyl group with a terminal hydroxyl of a growing chain. The Mn, P
b, and Zn acetates have shown comparable high catalytic activities; ho
wever, the Mn selectivity to give oligomers with hydroxyl-hydroxyl ter
minal groups is better and similar to that shown by Co and Mg acetate,
at a lower activity. Sb2O3 has a very low activity in transesterifica
tion but this activity could be important to eliminate the residual te
rminal methyl group during the polycondensation step. The catalytic ac
tivity of the mixture of Mg, Mn, and Zn acetate was greater than that
shown by each component the mixture, while its selectivity was compara
ble with that of Mn and Mg acetate. (C) 1996 John Wiley & Sons, Inc.