Three different approaches were adopted to study the gas phase behavior of
plasmas. The former is based on a detailed kinetic model, the second on the
traditional thermodynamic equilibrium assumption and the latter derives fr
om statistical thermodynamics. In particular, the extension of the statisti
cal fragmentation approach, originally developed for photo-ionization syste
ms, to plasma enhanced chemical vapor deposition reactors was considered fo
r the first time. Among the different systems studied were hydrocarbon and
chloro-hydrocarbon plasmas. The aim of the work was to develop a reliable s
tatistical thermodynamic approach apt to study the chemical reactivity of p
lasmas starting only from thermodynamic data. The enthalpies and entropies
of formation of the considered compounds were either taken from the literat
ure or calculated through quantum chemistry. Finally the predictions of the
three approaches were compared with the;available literature data and the
advantages and errors implicit in each approach were discussed.