Influence of Hydrophobicity on Polyelectrolyte Complexation

• Published in: Macromolecules Vol. 50; no. 23; pp. 9417 - 9426
• Main Authors: Sadman, Kazi, Wang, Qifeng, Chen, Yaoyao, Keshavarz, Bavand, Jiang, Zhang, Shull, Kenneth R
• Format: Journal Article
• Language: English
• Published: United States American Chemical Society 12-12-2017
• Subjects: complexation; hydrophobicity; MATERIALS SCIENCE; polyelectrolyte; rheology
• ISSN: 0024-9297; 1520-5835
• DOI: 10.1021/acs.macromol.7b02031

Polyelectrolyte complexes are a fascinating class of soft materials that can span the full spectrum of mechanical properties from low-viscosity fluids to glassy solids. This spectrum can be accessed by modulating the extent of electrostatic association in these complexes. However, to realize the full potential of polyelectrolyte complexes as functional materials, their molecular level details need to be clearly correlated with their mechanical response. The present work demonstrates that by making simple amendments to the chain architecture, it is possible to affect the salt responsiveness of polyelectrolyte complexes in a systematic manner. This is achieved by quaternizing poly­(4-vinylpyridine) (QVP) with methyl, ethyl, and propyl substituentsthereby increasing the hydrophobicity with increasing side chain lengthand complexing them with a common anionic polyelectrolyte, poly­(styrene­sulfonate). The mechanical behavior of these complexes is compared to the more hydrophilic system of poly­(styrene­sulfonate) and poly­(diallyldimethyl­ammonium) by quantifying the swelling behavior in response to salt stimuli. More hydrophobic complexes are found to be more resistant to doping by salt, yet the mechanical properties of the complex remain contingent on the overall swelling ratio of the complex itself, following near universal swelling–modulus master curves that are quantified in this work. The rheological behaviors of QVP complex coacervates are found to be approximately the same, only requiring higher salt concentrations to overcome strong hydrophobic interactions, demonstrating that hydrophobicity can be used as an important parameter for tuning the stability of polyelectrolyte complexes in general, while still preserving the ability to be processed “saloplastically”.