In this work, five different techniques: dilute solution viscometry, differential scanning calorimetry (DSC), dynamic mechanical analysis (DMA), Fourier transform infrared spectroscopy (FT-IR), and scanning electronic microscopy (SEM) were employed in order to evaluate interactions of amorphous poly(vinyl chloride) (PVC) and semi-crystalline poly(ethylene oxide) (PEO) in solution and solid state. The results varied significantly from one experimental technique to another. The positive interactions between the investigated polymers were found over the whole composition range only in solution. However, in the solid state, by DSC and DMA analysis, the positive interactions were found only at elevated PVC content, while FT-IR and SEM analysis could not confirm interactions between the investigated polymers.

The thermal degradation of poly(vinyl chloride)/acrylonitrile–butadiene–styrene (PVC/ABS) blends of different compositions was investigated by means of isothermal thermogravimetric analysis at temperatures of 210°–240°C in flowing atmosphere of air. The Flynn equation, the method of stationary point, and kinetic equation using the Prout–Tompkins model proved to be satisfactory in describing the thermooxidative degradation in the range of 5–30% conversions. The apparent activation energy E and preexponential factor Z were calculated for all compositions of PVC/ABS blends. The ratios E/ln Z are constant for pure and modified PVC and point to the unique mechanism of degradation process. Upon increasing the ratio of ABS in the PVC/ABS blend up to 50%, only the rate of the process is changed; the mechanism remains unchanged. © 1999 John Wiley & Sons, Inc. J Appl Polym Sci 71: 833–839, 1999