Loading…

Synthesis and rheological properties of an associative star polymer in aqueous solutions

Rheological properties of aqueous solutions and hydrogels formed by an amphiphilic star block copolymer, poly(acrylic acid)- block-polystyrene (PAA 54- b-PS 6) 4, were investigated as a function of the polymer concentration ( C p), temperature, and added salt concentration. The water-soluble polymer...

Full description

Saved in:
Bibliographic Details
Published in:Polymer (Guilford) 2007-06, Vol.48 (14), p.4087-4096
Main Authors: Hietala, Sami, Mononen, Pekka, Strandman, Satu, Järvi, Paula, Torkkeli, Mika, Jankova, Katja, Hvilsted, Søren, Tenhu, Heikki
Format: Article
Language:English
Subjects:
Citations: Items that this one cites
Items that cite this one
Online Access:Get full text
Tags: Add Tag
No Tags, Be the first to tag this record!
Description
Summary:Rheological properties of aqueous solutions and hydrogels formed by an amphiphilic star block copolymer, poly(acrylic acid)- block-polystyrene (PAA 54- b-PS 6) 4, were investigated as a function of the polymer concentration ( C p), temperature, and added salt concentration. The water-soluble polymer synthesised by atom transfer radical polymerization (ATRP) was found to form hydrogels at room temperature at polymer concentrations, C p, over 22 g/L due to the interpolymer hydrophobic association of the PS blocks. Increasing C p leads to stronger elastic networks at room temperature that show a gel-to-solution transition with increasing temperature. Increase of ionic strength decreases the moduli compared with the pure hydrogel but did not affect the gel–sol transition temperature significantly. Small-angle X-ray experiments showed two distinct scattering correlation peaks for samples above the gelling C p, which indicates the aggregates formed due to hydrophobic association. Upon heating the intensity of the scattering correlation peaks was found to decrease indicating the loss of the network structure due to thermal motion.
ISSN:0032-3861
1873-2291
DOI:10.1016/j.polymer.2007.04.069