摘要
Molecular dynamics simulation of the relaxation at 300 K of a fully extended polyethylene chain of 800 CH2 units has been carried out by following the changes in morphology, van der Waals energy, radius of gyration in the sense of mechanics and gyration radius in the sense of Flory, population of transconformation and orientation factor. The relaxation went through three stages: (1) relaxation from the morphology of a straight rod of 100 nm length to the morphology close to a random coil of gyration radius 5.9 nm in 110 ps; (2) collapse of the morphology of a coil to a highly compact globule close to a sphere of gyration radius 1.3 nm after 178 ps as the result of intersegmental van der Waals attractive interactions; (3) lateral ordering of the folded chain segments in the globule without appreciable changes in the chain dimension up to 1600 ps, the time limit of present simulation. Nearly complete relaxation of local segmental orientation was performed much faster than the relaxation of globule chain orientation even for a single chain of low degree of polymerization and at a temperature some 155 degrees C above its T-g. The lateral ordering of the chain segments during the period 178 to 680 ps of the simulation time was found to obey the Avrami equation with an Avrami index of 1.44.
Molecular dynamics simulation of the relaxation at 300 K of a fully extended polyethylene chain of 800 CH2 units has been carried out by following the changes in morphology, van der Waals energy, radius of gyration in the sense of mechanics and gyration radius in the sense of Flory, population of transconformation and orientation factor. The relaxation went through three stages: (1) relaxation from the morphology of a straight rod of 100 nm length to the morphology close to a random coil of gyration radius 5.9 nm in 110 ps; (2) collapse of the morphology of a coil to a highly compact globule close to a sphere of gyration radius 1.3 nm after 178 ps as the result of intersegmental van der Waals attractive interactions; (3) lateral ordering of the folded chain segments in the globule without appreciable changes in the chain dimension up to 1600 ps, the time limit of present simulation. Nearly complete relaxation of local segmental orientation was performed much faster than the relaxation of globule chain orientation even for a single chain of low degree of polymerization and at a temperature some 155 degrees C above its T-g. The lateral ordering of the chain segments during the period 178 to 680 ps of the simulation time was found to obey the Avrami equation with an Avrami index of 1.44.
