Direct observation of the transition from free to constrained single-segment motion in entangled polymer melts.
نویسندگان
چکیده
We report a direct determination of the time dependent mean-squared segment displacement of a polymer chain in the melt covering the transition from free to constraint Rouse relaxation along the virtual tube of the reptation model. This has been achieved by a neutron spin-echo (NSE) measurement of the segmental self-correlation function as conveyed by the spin-incoherent scattering from two fully protonated polymer melts, polyethylene and polyethylene propylene. Within the scenario of de Gennes reptation model a transition of the time dependence of segmental mean-squared displacements from proportional, variant t(1/2) to proportional, variant t(1/4) is expected and clearly corroborated by the incoherent NSE results.
منابع مشابه
Note: A simple picture of subdiffusive polymer motion from stochastic simulations.
Entangled polymer solutions and melts exhibit unusual frictional properties. In the entanglement limit self-diffusion coefficient of long flexible polymers decays with the second power of chain length and viscosity increases with 3–3.5 power of chain length.1 It is very difficult to provide detailed molecular-level explanation of the entanglement effect.2 Perhaps, the problem of many entangled ...
متن کاملProbabilistic phase space trajectory description for anomalous polymer dynamics.
It has been recently shown that the phase space trajectories for the anomalous dynamics of a tagged monomer of a polymer--for single polymeric systems and phenomena such as phantom Rouse, self-avoiding Rouse, and Zimm ones, reptation, and translocation through a narrow pore in a membrane, as well as for many polymeric systems such as polymer melts in the entangled regime--are robustly described...
متن کاملLong-lived interchain contacts in polymer melts
We will study time dependence of interchain contacts in entangled and unentangled polymer melts. We find that ‘‘clusters’’ of contacts in entangled melts persist in time up to at least 0.2 of the longest relaxation time. The clusters of contacts in un-entangled melts disappear and reappear on at least two orders of magnitude shorter time scale. We also examine time-dependent correlation functio...
متن کاملHopping Diffusion of Nanoparticles in Polymer Matrices
We propose a hopping mechanism for diffusion of large nonsticky nanoparticles subjected to topological constraints in both unentangled and entangled polymer solids (networks and gels) and entangled polymer liquids (melts and solutions). Probe particles with size larger than the mesh size ax of unentangled polymer networks or tube diameter ae of entangled polymer liquids are trapped by the netwo...
متن کاملPhase stability and dynamics of entangled polymer–nanoparticle composites
Nanoparticle-polymer composites, or polymer-nanoparticle composites (PNCs), exhibit unusual mechanical and dynamical features when the particle size approaches the random coil dimensions of the host polymer. Here, we harness favourable enthalpic interactions between particle-tethered and free, host polymer chains to create model PNCs, in which spherical nanoparticles are uniformly dispersed in ...
متن کاملذخیره در منابع من
با ذخیره ی این منبع در منابع من، دسترسی به آن را برای استفاده های بعدی آسان تر کنید
عنوان ژورنال:
- Physical review letters
دوره 90 5 شماره
صفحات -
تاریخ انتشار 2003