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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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Formamide as a Robust Alternative to Water for Plasticizing Polyelectrolyte Complexes
Polyelectrolyte complexes, PECs, are glassy and brittle when dry but may be plasticized with water. Though hydrated PECs contain a high proportion of water, many still exhibit a glass transition in the 0 to 100 oC range. The apparently unique effectiveness of water as a plasticizer of PECs has been an obstacle to further developments in applications and in fundamental studies of PEC properties. In this work it is shown that formamide is an excellent and even superior solvent for plasticizing PECs, substantially decreasing glass transition temperatures relative to those of hydrated PECs when formamide is used as a solvent instead. The affinities of PECs for water and formamide, indicated by the (exothermic) enthalpies of solvent swelling of dry PECs, are comparable. Ion transport dynamics revealed similar lifetimes, about 1 ns, of charge pairs within a PEC solvated with water compared to formamide, despite the differences in their dielectric constants. Ion transport dynamics, which depend on the mobility of pendant groups, have lower cooperativity than those of the polymer backbone. The use of formamide is a significant experimental variable for reducing the glass transition temperature/viscosity of complexed polyelectrolytes and can turn a solidlike hydrated complex into a fluidlike coacervate.
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- Award ID(s):
- 2103703
- PAR ID:
- 10621414
- Publisher / Repository:
- American Chemical Society
- Date Published:
- Journal Name:
- Macromolecules
- Volume:
- 57
- Issue:
- 19
- ISSN:
- 0024-9297
- Page Range / eLocation ID:
- 9367 to 9378
- Format(s):
- Medium: X
- Sponsoring Org:
- National Science Foundation
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- Free Publicly Accessible Full Text
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Accepted Manuscript1.0
- Journal Article:
- https://doi.org/10.1021/acs.macromol.4c01691
