Flow-Induced Orientation and Stretching of Entangled Polymers in the Framework of Nonequilibrium Thermodynamics

2016 ◽  
Vol 49 (8) ◽  
pp. 3161-3173 ◽  
Author(s):  
Pavlos S. Stephanou ◽  
Ioanna Ch. Tsimouri ◽  
Vlasis G. Mavrantzas
2020 ◽  
Vol 2 (1) ◽  
Author(s):  
Robin J. Dolleman ◽  
Gerard J. Verbiest ◽  
Yaroslav M. Blanter ◽  
Herre S. J. van der Zant ◽  
Peter G. Steeneken

2020 ◽  
Vol 2 (1) ◽  
Author(s):  
Olli-Pentti Saira ◽  
Matthew H. Matheny ◽  
Raj Katti ◽  
Warren Fon ◽  
Gregory Wimsatt ◽  
...  

Author(s):  
Rodrigo E. Teixeira ◽  
Richard S. Graham

The visco-elastic properties of entangled polymer liquids arise from molecular-scale topological interactions and stochastic fluctuations under flow. Here, the evolutions of individual entangled polymers were observed in rheologically relevant shear flow histories. We uncover a high degree of molecular individualism and broad conformational distributions resulting from incessant stretch-collapse cycles. The data and insights of the present study may lead to improved molecular-level models and constitutive equations. These tools, in turn, may enable the rational design of novel materials with properties tailored to accomplish specific tasks such as high-pressure vessels and piping with greater safety margins and cost-effectiveness.


Author(s):  
F. Eugene Yates ◽  
Laurel A. Benton

ABSTRACTThe flow of time can be conceptualized either as a cycle or an arrow. We offer a combined view: a helix. Chronological age (geophysical time reference) is not necessarily identical to biological age (internal time reference), and aging does not necessarily imply senescence. A new scheme of senescence, based on homeodynamics (nonlinear mechanics and nonequilibrium thermodynamics), is introduced as a plausible physical basis for understanding senescence. We propose that energy throughput, initially constructive of forms and functions, becomes destructive once most of the available degrees of freedom have been “frozen out” by the construction. Senescence becomes manifested at that point.


2000 ◽  
Vol 14 (32) ◽  
pp. 3881-3895 ◽  
Author(s):  
FRANCO FERRARI ◽  
HAGEN KLEINERT ◽  
IGNAZIO LAZZIZZERA

We formulate a field theory capable of describing a canonical ensemble of N polymers subjected to linking number constraints in terms of Feynman diagrams.


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