Please use this identifier to cite or link to this item: http://dx.doi.org/10.14279/depositonce-6222
Main Title: Concentration dependent effects of urea binding to poly(N-isopropylacrylamide) brushes: a combined experimental and numerical study
Author(s): Micciulla, Samantha
Michalowsky, Julian
Schroer, Martin A.
Holm, Christian
von Klitzing, Regine
Smiatek, Jens
Type: Article
Language Code: en
Abstract: The binding effects of osmolytes on the conformational behavior of grafted polymers are studied in this work. In particular, we focus on the interactions between urea and poly(N-isopropylacrylamide) (PNIPAM) brushes by monitoring the ellipsometric brush thickness for varying urea concentrations over a broad temperature range. The interpretation of the obtained data is supported by atomistic molecular dynamics simulations, which provide detailed insights into the experimentally observed concentration-dependent effects on PNIPAM-urea interaction. In particular, in the low concentration regime (c(u) <= 0.5 mol L-1) a preferential exclusion of urea from PNIPAM chains is observed, while in the high concentration regime (2 <= c(u) <= 7 mol L-1) a preferential binding of the osmolyte to the polymer surface is found. In both regimes, the volume phase transition temperature (T-tr) decreases with increasing urea concentration. This phenomenon derives from two different effects depending on urea concentration: (i) for c(u) <= 0.5 mol L-1, the decrease of T-tr is explained by a decrease of the chemical potential of bulk water in the surrounding aqueous phase; (ii) for c(u) >= 2 mol L-1, the lower T-tr is explained by the favorable replacement of water molecules by urea, which can be regarded as a cross-linker between adjacent PNIPAM chains. Significant effects of the concentration-dependent urea binding on the brush conformation are noticed: at c(u) <= 0.5 mol L-1, although urea is loosely embedded between the hydrated polymer chains, it enhances the brush swelling by excluded volume effects. Beyond 0.5 mol L-1, the stronger interaction between PNIPAM and urea reduces the chain hydration, which in combination with cross-linking of monomer units induces the shrinkage of the polymer brush.
URI: https://depositonce.tu-berlin.de//handle/11303/6883
http://dx.doi.org/10.14279/depositonce-6222
Issue Date: 2016
Date Available: 24-Oct-2017
DDC Class: 540 Chemie und zugeordnete Wissenschaften
Sponsor/Funder: DFG, EXC 310, Simulationstechnik
DFG, SFB 716, Dynamische Simulation von Systemen mit großen Teilchenzahlen
DFG, GRK 1524, Self-Assembled Soft-Matter Nanostructures at Interfaces
Creative Commons License: https://creativecommons.org/licenses/by-nc/3.0/
Journal Title: Physical chemistry, chemical physics
Publisher: Royal Society of Chemistry
Publisher Place: Cambridge
Volume: 18
Issue: 7
Publisher DOI: 10.1039/c5cp07544k
Page Start: 5324
Page End: 5335
EISSN: 1463-9084
ISSN: 1463-9076
Appears in Collections:Institut für Chemie » Publications

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