Coca-Hidalgo José Javier, Recillas-Mota Maricarmen, Fernández-Quiroz Daniel, Lizardi-Mendoza Jaime, Peniche-Covas Carlos, Goycoolea Francisco M, Argüelles-Monal Waldo M
Centro de Investigación en Alimentación y Desarrollo, Hermosillo 83304, Mexico.
Departamento de Ingeniería Química y Metalurgia, Universidad de Sonora, Hermosillo 83000, Mexico.
Polymers (Basel). 2024 Jun 2;16(11):1575. doi: 10.3390/polym16111575.
-alkyl-substituted polyacrylamides exhibit a thermal coil-to-globule transition in aqueous solution driven by an increase in hydrophobic interactions with rising temperature. With the aim of understanding the role of -alkyl substituents in the thermal transition, this study focuses on the molecular interactions underlying the phase transition of poly(-diethylacrylamide---ethylacrylamide) random copolymers. Poly(-diethylacrylamide) (PDEAm), poly(-ethylacrylamide) (PNEAm), and their random copolymers were synthesized by free radical polymerization and their chemical structure characterized spectroscopically. It was found that the values of the cloud-point temperature increased with PNEAm content, and particle aggregation processes took place, increasing the negative charge density on their surface. The cloud-point temperature of each copolymer decreased with respect to the theoretical values calculated assuming an absence of interactions. It is attributed to the formation of intra- and interchain hydrogen bonding in aqueous solutions. These interactions favor the formation of more hydrophobic macromolecular segments, thereby promoting the cooperative nature of the transition. These results definitively reveal the dominant mechanism occurring during the phase transition in the aqueous solutions of these copolymers.
烷基取代的聚丙烯酰胺在水溶液中表现出热卷曲-球状转变,这种转变是由温度升高时疏水相互作用的增强所驱动的。为了理解烷基取代基在热转变中的作用,本研究聚焦于聚(N,N-二乙基丙烯酰胺-N-乙基丙烯酰胺)无规共聚物相变背后的分子相互作用。通过自由基聚合合成了聚(N,N-二乙基丙烯酰胺)(PDEAm)、聚(N-乙基丙烯酰胺)(PNEAm)及其无规共聚物,并通过光谱对其化学结构进行了表征。发现浊点温度值随PNEAm含量的增加而升高,且发生了颗粒聚集过程,增加了其表面的负电荷密度。相对于假设不存在相互作用时计算出的理论值,每种共聚物的浊点温度均降低。这归因于在水溶液中形成了链内和链间氢键。这些相互作用有利于形成更多疏水的大分子链段,从而促进转变的协同性质。这些结果明确揭示了这些共聚物水溶液相变过程中发生的主导机制。