Related Experiment Video
Updated: Aug 6, 2026

Synthesis of Cyclic Polymers and Characterization of Their Diffusive Motion in the Melt State at the Single Molecule Level
Published on: September 26, 2016
Non-equilibrium conformations of dilute star polymers in shear flow
Xiaoyan Wang1, Anukta Datta2, Siobhan Powers2
1Department of Chemical and Biological Engineering, Rensselaer Polytechnic Institute, Troy, New York 12180, USA.
None:
Polymer topology influences the structural and dynamic behavior of macromolecules, particularly under non-equilibrium conditions such as shear flow. As a result, conventional Gaussian chain models fail to capture the complex deformation and relaxation dynamics of polymers with branched architectures. In this study, we present a combination of Brownian dynamics simulations with Gram-Charlier (G-C) expansion analysis to quantify non-Gaussian features using two cumulant-based metrics: the standard deviation σ of the one-dimensional projected configurational distribution, where larger values indicate greater deformation, and the normalized fourth cumulant κ4/σ4, where larger values indicate stronger non-Gaussianity. Focusing on linear and star polymers in dilute solution, we systematically investigate how molecular architecture, finite extensibility, and hydrodynamic interactions (HI) influence their deformation and conformational response in shear flow. Our findings reveal that star polymers exhibit constrained global extension but enhanced local stretching near the core, resulting in reduced deviations from Gaussian behavior compared to linear chains. Finite extensibility imposes an upper limit on bond extension, which suppresses configurational deformation at high shear rates and leads to a non-monotonic trend in κ4/σ4. By contrast, hydrodynamic interactions introduce long-range segmental coupling that enhances coordinated motion and amplifies non-Gaussian character, resulting in higher values of κ4/σ4 under strong shear flow. Together, these results establish a robust framework for characterizing the influence of polymer topology on non-equilibrium conformations, offering new insights into the mechanics of branched polymer systems under flow.
Related Concept Videos
Conformations of Cyclohexane
The chair form is the most stable and derives its name from its resemblance to the “easy chair.” In the chair conformation, two carbon atoms are arranged out-of-plane — one above and one below, minimizing the torsional strain. In the chair form, the bond angle is very close to the ideal tetrahedral value,...
Conformations of Ethane and Propane
Staggered conformation is a low energy and more stable conformation with the C-H bonds on the front carbon placed at 60°dihedral angles relative to the C-H bonds on the back carbon, leading to a reduced torsional strain. In staggered ethane, the...
Molecular Weight of Step-Growth Polymers
As the step-growth polymerization involves step-wise condensation of monomers, the molecular weight also builds up eventually. Consequently, high molecular weight polymers are obtained at the late stages of the polymerization, where 99% of monomers have been consumed.
The extent of the...
Determination of Molar Masses of Polymers II
Polymer Classification: Stereospecificity
Problem Solving on Stress and Strain

