A series of blends of poly(vinyl chloride) (PVC) with (1) poly(methyl metha
crylate) (PMMA) or (2) polyoxymethylene (POM), with lithium acetate as a st
abilizing agent, was investigated by differential scanning calorimetry (DSC
), scanning electron microscopy (SEM), and thermogravimetric analysis (TGA)
, either alone or coupled with Fourier transform infrared (FTIR) spectrosco
py. It was found that lithium acetate has a significant effect on the therm
al properties of blends under investigation. It causes the initial decompos
ition temperatures to increase by about 60-150 degrees C for PVC-POM blends
, a substantial suppression of the volatile products evolution for PVC/PMMA
blends, and an improvement in the surface morphology for both polymer syst
ems by lowering the degree of roughness. The origin of these effects was di
scussed by analysis of the intermolecular complexation between metal salt a
nd PVC structural arrangements in the blends. Such interactions may lead to
the formation of long-range, directional-specific structural regularities,
which in turn thermally stabilize the whole system (strong interactions mo
del). (C) 1999 John Wiley & Sons, Inc.