Non-NIPAM Based Microgels: Tuning the Volume Phase Transition by Copolymerisation and by Particle Architecture

Thomas Hellweg Michael Zeiser Bastian Wedel
Physical and Biophysical Chemistry, Bielefeld University, Bielefeld, Germany

Over the last decade smart microgels have been increasingly recognized as potential building blocks for photonic materials, catalytic carriers and sensors.[1] This applicability is based on the fairly unlimited tuning possibilities of swelling properties as well as scattering properties of those particles. The present contribution studies non-(N-isopropyl acrylamide)-based core-shell microgels that exhibit a linear thermoresponsive behavior in a temperature range between 25°C and 40°C. It is the combination of distinct materials in core and shell, that gives the particles this unique property. For the first part of our study we synthesized statistical copolymers from N-n-proplyacrylamide (NNPAM) and N-isopropylmethacrylamide (NIPMAM) and study their behavior by means of scattering techniques [2]. Moreover, we have synthesized core-shell microgels from these monomers with differently cross-linked cores. This approach was inspired by the work of the Richtering group[3]. Photon correlation spectroscopy allowed us to study the temperature dependent swelling, which revealed a significant influence of the core properties on the overall core-shell behavior. A major finding of these experiments is that the swelling becomes linear dependent on temperature and the crosslinker content of the core is directly related to the linear response. The core-shell particles behave piezo-like and might have potential as actuators [4]. The internal structure of the particles is followed by means of small angle neutron scattering (SANS) revealing heterogeneities during the transitions of the NNPAM shell.

[1] A. Fernandez-Nieves, H. Wyss, J. Mattsson and D. Weitz, Microgel Suspensions, Wiley VCH, Weinheim, Germany, 2011

[2] B. Wedel, M. Zeiser, and T. Hellweg, Zeitschrift f. Physikalische Chemie, 2012, 226, 737748

[3] I. Berndt and W. Richtering Macromolecules 2003, 36, 8780

[4] M. Zeiser, I. Freudensprung, and T. Hellweg, Polymer, 2012, 53,6096

thomas.hellweg@uni-bielefeld.de








 




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