Non-additive Ion Effects on the Coil-Globule Equilibrium of a Generic Uncharged Polymer
Abstract
Mixtures of weakly and strongly hydrated anions induce non-additive changes in the LCST of thermoresponsive polymers such as Poly(N-isopropylacrylamide) (PNIPAM) and PEO. Large-scale atomistic simulations of PNIPAM-NaI-NaSO mixtures show that these effects arise from the interplay between favorable PNIPAM-iodide interactions and the depletion of strongly hydrated sulfate ions. Here, we investigate whether chemically specific polymer-anion interactions are necessary to reproduce such behavior. To this end, we study the coil-to-globule transition of a generic uncharged linear polymer with non-specific polymer-water and polymer-ion van der Waals interactions in atomistic aqueous solutions of single and mixed salts. We perform simulations at fixed concentrations of the strongly hydrated salt, NaSO, and increasing concentrations of weakly hydrated salts, NaSCN and NaI. The generic polymer qualitatively reproduces experimental trends in both pure NaSCN and NaSO solutions, as well as in mixed salt solutions. The model captures the mutual reinforcement between SCN accumulation near the polymer and SO depletion that gives rise to non-additive behavior, consistent with atomistic simulations in PNIPAM solutions. These features become more pronounced with increasing background salt concentration and are further enhanced upon replacing SCN with I, owing to weaker polymer-iodide interactions. Our results demonstrate that non-specific polymer-ion interactions are sufficient to reproduce non-additive features, highlighting the dominant role of bulk ion-ion and ion-water interactions.
Source: arXiv:2603.26555v1 - http://arxiv.org/abs/2603.26555v1 PDF: https://arxiv.org/pdf/2603.26555v1 Original Link: http://arxiv.org/abs/2603.26555v1