Wang Peixi, Zheng Tianle, Reitenbach Julija, Wegener Simon A, Huber Linus F, Kreuzer Lucas P, Liang Suzhe, Cubitt Robert, Cheng Ya-Jun, Xu Tonghui, Hildebrand Viet, Laschewsky André, Papadakis Christine M, Müller-Buschbaum Peter
Chair for Functional Materials, Department of Physics, TUM School of Natural Sciences, Technical University of Munich, James-Franck-Str. 1, 85748, Garching, Germany.
Heinz Maier-Leibnitz Zentrum (MLZ), Technical University of Munich, Lichtenbergstr. 1, 85748, Garching, Germany.
Adv Sci (Weinh). 2025 Feb;12(8):e2408073. doi: 10.1002/advs.202408073. Epub 2024 Dec 31.
Understanding the salt effects on solvation behaviors of thermoresponsive polymers is crucial for designing and optimizing responsive systems suitable for diverse environments. In this work, the effect of potassium salts (CHCOOK, KCl, KBr, KI, and KNO) on solvation dynamics of poly(4-(N-(3'-methacrylamidopropyl)-N,N-dimethylammonio) butane-1-sulfonate) (PSBP), poly(N-isopropylmethacrylamide) (PNIPMAM), and PSBP-b-PNIPMAM films is investigated under saturated water and mixed water/methanol vapor via advanced in situ neutron/optical characterization techniques. These findings reveal that potassium salts enhance the films' hygroscopicity or methanol-induced swellability. Interestingly, the anions effects do not mirror the empirical Hofmeister series, which describes the salting-in effects for such polymers in dilute aqueous solution, particularly evident in PSBP films with an approximately inverted order. PNIPMAM and PSBP-b-PNIPMAM exhibit pronounced deviations from such an inverted correlation and vary somewhat for water-rich and methanol-rich atmospheres. Molecular dynamics (MD) simulations suggest that the observed orders of solvation result from the accessibility of the hydrated solvation shells close to the PSBP-b-PNIPMAM chains.
了解盐对热响应性聚合物溶剂化行为的影响对于设计和优化适用于不同环境的响应系统至关重要。在这项工作中,通过先进的原位中子/光学表征技术,研究了钾盐(CHCOOK、KCl、KBr、KI和KNO)对聚(4-(N-(3'-甲基丙烯酰胺基丙基)-N,N-二甲基铵)丁烷-1-磺酸盐)(PSBP)、聚(N-异丙基甲基丙烯酰胺)(PNIPMAM)以及PSBP-b-PNIPMAM薄膜在饱和水和水/甲醇混合蒸汽中的溶剂化动力学的影响。这些发现表明,钾盐增强了薄膜的吸湿性或甲醇诱导的溶胀性。有趣的是,阴离子效应并不符合描述此类聚合物在稀水溶液中的盐溶效应的经验性霍夫迈斯特序列,这在PSBP薄膜中尤为明显,其顺序近似颠倒。PNIPMAM和PSBP-b-PNIPMAM与这种颠倒的相关性存在明显偏差,并且在富水和富甲醇气氛中有所不同。分子动力学(MD)模拟表明,观察到的溶剂化顺序是由靠近PSBP-b-PNIPMAM链的水合溶剂化壳层的可及性导致的。