Journal of Polymer Science Part B: Polymer Physics
Copyright © 2012 Wiley Periodicals, Inc., A Wiley Company
Online ISSN: 1099-0488
Associated Title(s): Journal of Polymer Science Part A: Polymer Chemistry
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J. Polym. Sci. B Polym. Phys. publishes papers on the physics of polymers, including applications, theory and modeling, and experiments. 2014 ISI Impact Factor: 3.830.
- Cellulose nanocrystals and related nanocomposites: Review of some properties and challenges
Mariano et al., DOI: 10.1002/polb.23490
- Flexible, stretchable, and patchable organic devices integrated on freestanding polymeric substrates
Kim et al., DOI: 10.1002/polb.23662
- Structure of sodium carboxymethyl cellulose aqueous solutions: A SANS and rheology study
Lopez et al., DOI: 10.1002/polb.23657
Recently Published Articles
- Multimaterial hydrogel with widely tunable elasticity by selective photopolymerization of PEG diacrylate and epoxy monomers
Esben Kjær Unmack Larsen, Niels B. Larsen, Kristoffer Almdal, E. K. U. Larsen, N. B. Larsen and K. Almdal
Article first published online: 8 FEB 2016 | DOI: 10.1002/polb.24007
Multimaterial structures made from a poly(ethylene glycol) diacrylate and epoxy resin solution becomes selectively either a soft hydrogel or a stiff polymer when exposed to blue or UV light. Materials with graded mechanical properties spanning over two orders of magnitude result from varying the wavelength and time of the exposure.
- Constituent analysis of stress memory in semicrystalline polyurethane
Harishkumar Narayana, Jinlian Hu, Bipin Kumar and Songmin Shang
Article first published online: 8 FEB 2016 | DOI: 10.1002/polb.24000
A new approach is made in this study to unveil the total stress–strain components in the stress memory polymers. Stress memory behavior of semicrystalline polyurethane is analytically studied by quantifying the stress components in tensile mode of programming using constituent equations and a novel relaxed modulus (RM). This approach can help researchers to engineer the products needing memory stress more precisely in multidisciplinary areas by predicting their behavior accurately.
- Recovery stress and work output in hyperbranched poly(ethyleneimine)-modified shape-memory epoxy polymers
David Santiago, Albert Fabregat-Sanjuan, Francesc Ferrando and Silvia De la Flor
Article first published online: 3 FEB 2016 | DOI: 10.1002/polb.24004
Hyperbranched-modified shape-memory epoxy polymers are studied in order to determine their potential use as thermomechanical actuators. Shape memory effect is analysed under fully and partially constrained conditions to evaluate the recovery stress and mechanical work generated. Results revealed rapid recovery stress generation, very high recovery stresses (up to 7 MPa) and extremely high work densities (up to 750 kJ/m3). The network structure of shape-memory polymers was found to be a key factor for actuator-like applications.
- Molecular dynamics simulations of cation-controlled aggregation in fluorene–triarylamine copolymers
Meilin Li and Stefan Adams
Article first published online: 3 FEB 2016 | DOI: 10.1002/polb.23998
Molecular dynamics simulations of sulfonated fluorene–triarylamine hole conductor polymers containing a wide range of monovalent cations show that the variation in the degree of cation clustering with cation size controls polymer morphology, cation mobility and the time evolution of the energy landscape for charge transport. The resulting MD trajectories for each BAFS–cation system are analyzed with respect to the influence of the cation type on the ionic aggregation and related structural features that may affect the conduction mechanism.
- Phase separation in dilute polymer solutions at high-rate extension
Andrey V. Subbotin and Alexander N. Semenov
Article first published online: 3 FEB 2016 | DOI: 10.1002/polb.24005
Flow-induced demixing in polymer solutions is a widely known phenomenon observed both in shear and extension flows, particularly high-rate uniaxial extension of polymer solutions often accompanied by decomposition of polymeric filament from the solvent. We study the phase separation in polymer solutions under extension flow arisen above the coil to stretched coil transition. Based on the free energy analysis we show that the flow-induced orientation of polymer segments can drastically reduce the energy of their steric repulsion. As a result attraction between the chains gains more importance, and this effect leads to segregation of polymer from the solvent if the strain rate exceeds some critical value.