An extended Molecular-Dynamics study of the short-time "glassy" elasticity
exhibited by a polymer melt of linear fully-flexible chains above the glass
transition is presented. The focus is on the infinite-frequency shear modulus
G∞ manifested in the picosecond time scale and the relaxed plateau
Gp reached at later times and terminated by the structural relaxation. The
local stiffness of the interactions with the first neighbours of each monomer
exhibits marked distribution with average value given by G∞. In
particular, the neighbourhood of the end monomers of each chain are softer than
the inner monomers, so that G∞ increases with the chain length. Gp
is not affected by the chain length and is largely set by the non-bonding
interactions, thus confirming for polymer melts the conjecture formulated by
Tobolsky for glassy polymers.Comment: 18 pages, 6 figure