121
Views
3
CrossRef citations to date
0
Altmetric
Original Articles

Temperature-Dependent, High-Resolution Magic-Angle-Spinning (HRMAS) NMR Studies of Poly(N-isopropylacrylamide-co-acrylic Acid)

&
Pages 280-294 | Received 15 Jul 2011, Accepted 15 Sep 2011, Published online: 14 Feb 2012
 

Abstract

High-resolution magic-angle-spinning NMR spectroscopy is used to investigate the phase transition of poly(N-isopropylacrylamide-co-acrylic acid) hydrogels crosslinked with N,N’-methylene bisacrylamide, hereafter poly(NIPAAm-co-AAc). Van't Hoff ΔH and ΔS for polymer dehydration are derived from temperature-dependent NMR spectra, and the thermodynamic data strongly support a four-stage dehydration mechanism for pure poly(NIPAAm). Acrylic acid stabilizes the hydration sphere around the polymer chains. Reduced amounts of water released during the phase transition translates into smaller values for ΔH and ΔS. Enhanced rehydration kinetics for poly(NIPAAm-co-AAc) is attributed to water remaining in the samples at elevated temperatures, which may produce facile diffusion pathways and enable faster rehydration kinetics than poly(NIPAAm).

Acknowledgments

This work was supported by the University of Oklahoma and a CAREER Award from the National Science Foundation to CVR (CHE-0449622). CMB is indebted to Northeastern State University for partial support of the project.

Log in via your institution

Log in to Taylor & Francis Online

PDF download + Online access

  • 48 hours access to article PDF & online version
  • Article PDF can be downloaded
  • Article PDF can be printed
USD 61.00 Add to cart

Issue Purchase

  • 30 days online access to complete issue
  • Article PDFs can be downloaded
  • Article PDFs can be printed
USD 2,387.00 Add to cart

* Local tax will be added as applicable

Related Research

People also read lists articles that other readers of this article have read.

Recommended articles lists articles that we recommend and is powered by our AI driven recommendation engine.

Cited by lists all citing articles based on Crossref citations.
Articles with the Crossref icon will open in a new tab.