Polyether-polyester block copolymers having various polyetheramide contents were synthesized. Single glass transition intermediated in temperature between the glass transition temperatures of polyester and polyetheramide components was found for all of polyether-polyesters. The compositional variation of glass transition exhibited a similar trend to the predicted result of thermodynamic theory for compatible polymer blends. The incompatible pair of homopolyester and homopolyether was forced to be compatible after copolymerization. A modified theoretical prediction for the glass transition of copolymers based on the thermodynamic theory is proposed. Consistent results between theoretical prediction and experimental measurements were found. Unlike homopolyesters, the glass transition temperature of copolymer amorphous domains gradually decreases with crystallization time. An exclusion model for the crystallization of polyester segments in copolymers is proposed. The temperature width of the glass transition increases with crystallization time. The broadening towards the low temperature side in glass transition is interpreted as the evidence of crystallization-induced partial phase separation. Instead of forming macroscopic segregation, the excluded polyether segments resided in-between crystalline polyester lamellae and mix with amorphous polyesters to generate amorphous domains exhibiting concentration gradient along the lamellar basal surface normal. Further increasing the polyetheramide segment content brings the excluded polyetheramide segments to form domains among the crystallized polyester spherulites so as to inhibit the occurrence of spherulitic impingement.