The theory and application of mid-IR emission spectroscopy to the stud
y of the oxidation of single reactor particles of unstabilized polypro
pylene (0.4 to 40 mu g) is described. The rate of formation of carbony
l and gamma-lactone oxidation products is followed by FT-IR emission a
t 150 degrees C and is interpreted within a heterogeneous model of sol
id state oxidation. The results are compared with the reported chemilu
minescence from single polypropylene particles and evidence is present
ed for concerted oxidation when the particles are in close proximity.