Article
Spectral time moment analysis of microgel deswelling. Effect of the heating rate
Article first published online: 10 NOV 2008
DOI: 10.1002/polb.21615
Copyright © 2008 Wiley Periodicals, Inc.
Issue

Journal of Polymer Science Part B: Polymer Physics
Special Issue: The American Physical Society Division of Polymer Physics Special Issue
Volume 46, Issue 24, pages 2792–2802, 15 December 2008
Additional Information
How to Cite
Streletzky, K. A. and Mckenna, J. T. (2008), Spectral time moment analysis of microgel deswelling. Effect of the heating rate. J. Polym. Sci. B Polym. Phys., 46: 2792–2802. doi: 10.1002/polb.21615
Publication History
- Issue published online: 10 NOV 2008
- Article first published online: 10 NOV 2008
- Manuscript Revised: 3 OCT 2008
- Manuscript Accepted: 3 OCT 2008
- Manuscript Received: 7 AUG 2008
Funded by
- Cottrell Science Award from the Research Corporation
- Engaged Learning Undergraduate Student Award from CSU
- Abstract
- Article
- References
- Cited By
Keywords:
- diffusion;
- dynamic light scattering;
- microgels;
- polysaccharides;
- stimuli-sensitive
Abstract
Microgel nanoparticles were synthesized in aqueous solutions of neutral polymer hydroxypropylcellulose (HPC) through the self-association of amphiphilic HPC molecules and the subsequent cross linking at room temperature. Dynamic Light Scattering was used to study the transport properties of HPC microgels below and above the volume phase transition. Highly nonexponential, multimodal microgel spectra were observed and successfully analyzed by spectral time moment analysis. This article expands earlier results and focuses on the effect of the heating rate on microgel deswelling. During the fast heating two identified microgel modes with apparent hydrodynamic radii (RH) of 25–30 nm and 400–650 nm collapse into one mode with RH = 100–150 nm. This indicates the shrinkage of microgel size distribution and an apparent decrease in the radius of larger microgels. During the slow heating, however, both microgel-identified modes remain present above Tc. Although equally represented below the transition, the dominance of larger microgels' mode increases almost two fold with rising temperature above 40°C. Moreover, RH for this mode increases from 250–300 nm to about 800–850 nm with a multi-step temperature change from 40 to 42.5°C, indicating the growth (and not shrinkage) of microgels. The second mode is represented by the temperature independent RH, but its contribution goes down from about 50% to less than 10%. © 2008Wiley Periodicals, Inc. J Polym Sci Part B: Polym Phys 46: 2792–2802, 2008

1099-0488/asset/olbannerleft.jpg?v=1&s=a96d11b7617a61804e3ad92688329bda73fbfe9a)
1099-0488/asset/olbannerright.jpg?v=1&s=60d01780b5078fca6150d7f2b56b2e4f55393b67)