Th e t herm al deco mposition of variou s flu oro carbon p olymers were inv est iga,ted ; volatile p rodu cts of t he d ecomposition were d et ermined along with t he overall rates of volatili zation, a nd from t h ese rates t he acti vation energies were calculated for t he thermal deg radation r eactions. The t hermalJ y m ost stable of all t he poly mers t hus far st ud ied a re t he co mpletely flu orin ated o nes. H owever, e vid ence from a s t udy of t he dccomposition of h exafluorop ropy lene t elomers and from th e study of a copolym cr of t etra flu oroe thylene and hexafl uo ropropylene suggest s t hat the homopolymer of hexaflu o roprop ylene, if it co uld be m ad e, wou ld be quite unstable. The photoindu ced d ecomposi tion of polyt rifiu orochloroet hylene was also investigated , a nd estimates of t he activa tion energies wer e ob tain ed for the variou s elementar y step s of t he deco mposi tion m echanism:] Th e photoindu ced exp er imc nts indica ted that mu t ual termination of t he radical i nt erm ediates takes place and t hat a diff usion effect on d ep ropagation b cco mes pronoun ced below 250°C.