ABSTRACT:Gel-melting temperatures (T~) of ethylene-propylene random copolymer gels formed in n-hexane and n-octane were measured as a function of polymer concentration. The copolymers were heterogeneous in both composition and molecular weight. T~ obeyed well the thermodynamic theory derived by Takahashi, in which gel--->sol transition was treated as melting of crystalline junctions with fringed micelle-type morphology: Plots of 1/T~ vs. In V2N according to the theory were scaled on a common straight line when copolymers had similar propylene contents (PC), where V2 is the volume fraction of the copolymer in the gel and Nis the weight-average degree of polymerization. Quantitative analysis of the theory, including measurements of dilute solution properties, led to the results that average size of crystalline junction ( in number of ethylene units per crystalline sequence was ca. 11 for copolymers with PC= 22 wt%, 9 for PC= 26 and 27wt%, and 5 for PC=49wt%, and thus ( decreased with increasing PC. The junction sizes ( were reasonable order as compared with those estimated from X-ray diffractions.