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Bibliographic Details
Main Author: Monreal, Jorge
Format: Preprint
Published: 2016
Subjects:
Online Access:https://arxiv.org/abs/1609.05358
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author Monreal, Jorge
author_facet Monreal, Jorge
contents Experimental results from mechanical viscoelastic as well as dielectric relaxation times were compared to theoretical expectations utilizing polymer scaling theory. Viscoelastic relaxation of a hydrogel at 33% relative humidity fabricated from co-poly-L-(glutamic acid$_{4}$, tyrosine$_{1}$) [PLEY(4:1)] crosslinked with poly-L-lysine scaled with concentration according to reptation dynamics. High frequency dielectric relaxation of aqueous copolymer PLEY(4:1) scaled with concentration as an ideal chain and aqueous Poly-L-glutamic acid scaled as an extended chain. The study shows that two seemingly different measurement methods can yield information about the state of polymer chain conformation in situ.
format Preprint
id arxiv_https___arxiv_org_abs_1609_05358
institution arXiv
publishDate 2016
record_format arxiv
spellingShingle Polyelectrolyte Polypeptide Scaling Laws Via Mechanical and Dielectric Relaxation Measurements
Monreal, Jorge
Soft Condensed Matter
Experimental results from mechanical viscoelastic as well as dielectric relaxation times were compared to theoretical expectations utilizing polymer scaling theory. Viscoelastic relaxation of a hydrogel at 33% relative humidity fabricated from co-poly-L-(glutamic acid$_{4}$, tyrosine$_{1}$) [PLEY(4:1)] crosslinked with poly-L-lysine scaled with concentration according to reptation dynamics. High frequency dielectric relaxation of aqueous copolymer PLEY(4:1) scaled with concentration as an ideal chain and aqueous Poly-L-glutamic acid scaled as an extended chain. The study shows that two seemingly different measurement methods can yield information about the state of polymer chain conformation in situ.
title Polyelectrolyte Polypeptide Scaling Laws Via Mechanical and Dielectric Relaxation Measurements
topic Soft Condensed Matter
url https://arxiv.org/abs/1609.05358