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Updated: Jun 6, 2025
Cooling Rate Dependent Ellipsometry Measurements to Determine the Dynamics of Thin Glassy Films
Published on: January 26, 2016
Divalent cation effects in the glass transition of poly(diallyldimethylammonium)-poly(styrene sulfonate)
Tamunoemi Braide1, Suvesh Manoj Lalwani1, Chikaodinaka I Eneh1
1Artie McFerrin Department of Chemical Engineering, Texas A&M University, College Station, Texas 77840, USA. jodie.lutkenhaus@tamu.edu.
Abstract:
The assembly and dynamics of polyelectrolyte complexes (PECs) and polyelectrolyte multilayers (PEMs) are influenced by water content, pH, and salt concentration. However, the influence of divalent salts on the assembly of polyelectrolyte complexes remains unclear. This work showcases that divalent chloride salts directly impact the glass transition temperature and the ion-ion interactions within PECs. Here, poly(diallyldimethylammonium)-poly(styrene sulfonate) (PDADMA-PSS) PECs are assembled in solutions containing MgCl2 and CaCl2 (following the Hofmeister series). These PECs are studied for the cations' influence on physicochemical properties (glass transition, polymer composition, ion pairing) at varying salt concentrations (0.03 M, 0.10 M, 0.15 M, and 0.20 M). Modulated differential scanning calorimetry (MDSC) experiments demonstrate that PECs assembled with CaCl2 have a significantly higher glass transition temperature when compared to PECs assembled with MgCl2. Neutron activation analysis (NAA) and nuclear magnetic resonance (NMR) spectroscopy demonstrate that this difference is due to strong ion-specific effects influencing the ratio of intrinsic and extrinsic ion pairings in the system. Furthermore, this study demonstrates a universal linear relationship between the thermal transition and the number of water molecules surrounding oppositely charged polyelectrolyte-polyelectrolyte intrinsic ion pairs, even when the salt contains divalent cations. Ion-specific trends have implications on the glass transition and composition of PDADMA-PSS PECs. Divalent salts not only follow the trend of the Hofmeister series but also introduce bridging into the polyelectrolyte complex; however, the structural relaxation of the PEC remains the same. This study offers a bridge between divalent cation behavior on polymer assembly properties and its transition to industrial applications such as controlled drug delivery, sensors, and water purification.
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