Isostaticity and the Solidification of Semiflexible Polymer Melts
Document Type
Article
Publication Date
2017
Digital Object Identifier (DOI)
https://doi.org/10.1039/C7SM01442B
Abstract
Using molecular dynamics simulations of a tangent-soft-sphere bead-spring polymer model, we examine the degree to which semiflexible polymer melts solidify at isostaticity. Flexible and stiff chains crystallize when they are isostatic as defined by appropriate degree-of-freedom-counting arguments. Semiflexible chains also solidify when isostatic if a generalized isostaticity criterion that accounts for the slow freezing out of configurational freedom as chain stiffness increases is employed. The configurational freedom associated with bond angles (θ) can be associated with the characteristic ratio C∞ = (1 + 〈cos(θ)〉)/(1 − 〈cos(θ)〉). We find that the dependence of the average coordination number at solidification [Z(Ts)] on chains' characteristic ratio C∞ has the same functional form [Z ≃ a − b ln(C∞)] as the dependence of the average coordination number at jamming [Z(ϕJ)] on C∞ in athermal systems, suggesting that jamming-related phenomena play a significant role in thermal polymer solidification.
Was this content written or created while at USF?
Yes
Citation / Publisher Attribution
Soft Matter, 13, p. 7948-7952
Scholar Commons Citation
Plaza-Rivera, Christian O.; Nguyen, Hong T.; and Hoy, Robert S., "Isostaticity and the Solidification of Semiflexible Polymer Melts" (2017). Physics Faculty Publications. 116.
https://digitalcommons.usf.edu/phy_facpub/116
