A terminally anhydride functionalized polypropylene was synthesized vi
a the Alder Ene reaction from a low molecular weight amorphous polypro
pylene. A Lewis acid, SnCl2 . 2H(2)O, was found to catalyse the reacti
on, thereby improving anhydride content in the polymer for reaction co
nditions comparable to those in an extrusion environment, i.e, elevate
d temperature and short residence time. The reaction was carried out a
t 230 degrees C for 5 min in the presence of TEMPO, which acted as a f
ree radical trap, preventing maleic anhydride from being grafted onto
the backbone of the polypropylene. The product was characterized by se
veral techniques, including FTi.r. and n.m.r., to provide evidence of
the anhydride location on the chain. Several runs of varying catalyst
concentration have shown that an optimum in anhydride incorporation on
to the polypropylene exists. Examination of the system kinetics has sh
own that the overall order of the reaction remains second-order despit
e the presence of a catalyst. (C) 1997 Elsevier Science Ltd.