The basic crystallization and melting behavior of three aliphatic polyketones were studied using differential scanning calorimetry (DSC), wide-angle X-ray diffraction (WAXD), small-angle X-ray scattering (SAXS), and optical microscopy. One resin was a perfectly alternating copolymer of ethylene and carbon monoxide, while the other two resins were terpolymers in which 6 mol % propylene was substituted for ethylene. Small decreases in the melting point and percent crystallinity of these materials were displayed with repeated melting. This behavior was attributed to light crosslinking as a result of condensation reactions occurring at temperatures in the melting range. WAXS showed that, after cooling to room temperature, the crystalline form in the copolymer was the a-phase, while that in the terpolymers was the g-phase. Optical microscopy revealed that the materials produce both negative and mixed birefringence spherulites under the conditions studied. SAXS measurements showed that the lamella thickness was largely a function of the temperature of crystallization. Attempts were made to measure the equilibrium melting temperature of these resins using several available techniques. The best value of the equilibrium melting temperature was concluded to be 278 +/-2degreesC for the copolymer. The results varied over a wide range for the terpolymers, but it is suggested that appropriate values are of order 252degreesC for the terpolymers. Crystallization kinetics studies, carried out under isothermal conditions using DSC, were evaluated using the Avrami equation. Results showed the Avrami exponent to lie in the range of 2-3. Spherulite growth rates were interpreted in terms of the secondary nucleation theory of Lauritzen and Hoffman. A transition from regime II to regime III was discovered.