.

Showing posts with label Polymer. Show all posts
Showing posts with label Polymer. Show all posts

Monday, May 2, 2016

Swollen structure and electrostatic interactions of polyelectrolyte brush in aqueous solution

Daiki Murakami, Motoyasu Kobayashi, Yuji Higaki, Hiroshi Jinnai, Atsushi Takahara

Surface grafting of polyelectrolytes on materials brings about various significant changes in surface properties such as wettability, adhesion, and friction, because of their excellent hydrophilicity and unique intermolecular interactions that depend on the ionic strength of the solution. This review paper describes the characterization of the swollen structure and electrostatic interaction of polyelectrolyte brushes in aqueous solution by use of optical tweezers and neutron reflectivity, in order to discuss the dissociation of ionic groups and charge distribution in the polyelectrolyte brush. In addition, the spreading and structure of water on the polyelectrolyte brush surface were characterized by high spatial resolution IR spectroscopy.

DOI

Monday, August 1, 2011

Drag reduction by DNA-grafting for single microspheres in a dilute λ-DNA solution

Olaf Ueberschär, Carolin Wagner, Tim Stangner, Konstanze Kühne, Christof Gutsche and Friedrich Kremer

The fluid resistance of single micrometre-sized blank and DNA-grafted polystyrene microspheres under shear flow is compared in purified water and dilute λ-DNA solutions by means of optical tweezers experiments with a high spatial (±4 nm) and temporal (±0.2 ms) resolution. The measurement results show that the drag experienced by a colloid in a dilute λ-DNA solution (molecular weight of 48,502 bp per molecule, radius of gyration of 0.5 μm) is significantly decreased if the microsphere bears a grafted DNA brush. This newly discovered drag reduction effect is studied for different parameters, comprising the molecular weight of the grafted DNA molecules (250 bp, 1000 bp and 4000 bp), the concentration of the λ-DNA solution (11, 17 and 23 μg ml−1, all being significantly smaller than the critical entanglement concentration c*), the microsphere core diameter (2 μm, 3 μm and 6 μm) as well as the flow speed of the medium (10–50 μm s−1). The maximum extent of the drag reduction is found to amount to (60 ± 20)% compared to the λ-DNA-induced contribution on the drag acting on blank colloids. We propose a theoretical explanation of this effect based on the combination of the dynamic density functional theory of Rauscher and co-workers [Rauscher M. J. Phys.: Condens. Matter 2010;22:364109] and the stagnation length theory of polymer brushes, as it was established by Kim, Lobaskin et al. [Kim et al. Macromolecules 2008;42(10):3650–3655]. In particular, the solution of the Stokes equation (i.e., the Navier–Stokes equation for creeping flow) for the studied system yields a numerical prediction that is found to be in full accord with our experimental results within measurement uncertainty.

DOI

Thursday, March 24, 2011

The effective hydrodynamic radius of single DNA-grafted colloids as measured by fast Brownian motion analysis

Olaf Ueberschär, Carolin Wagner, Tim Stangner, Christof Gutsche and Friedrich Kremer

Optical tweezers accomplished with fast position detection enable one to carry out Brownian motion analysis of single DNA-grafted (grafting density: 1000 molecules per particle, molecular weight: 4000 bp) colloids in media of varying NaCl concentration. By that the effective hydrodynamic radius of the colloid under study is determined and found to be strongly dependent on the conformation of the grafted DNA chains. Our results compare well both with recent measurements of the pair interaction potential between DNA-grafted colloids (Kegler et al. Phys Rev Lett 2008; 100:118302) and with microfluidic studies (Gutsche et al. Microfluid Nanofluid 2006; 2:381-386). The observed scaling of the brush height with the ion concentration is in full accord with the theoretical predictions by Pincus, Zhulina, Birshtein and Borisov.

DOI