Velychkivska Nadiia, Starovoytova Larisa, Březina Václav, Hanyková Lenka, Hill Jonathan P, Labuta Jan
Department of NMR Spectroscopy, Institute of Macromolecular Chemistry AS CR, v.v.i., Heyrovsky Sq. 2, Prague 6 162 06, Czech Republic.
Faculty of Mathematics and Physics, Department of Macromolecular Physics, Charles University, V Holešovičkách 2, 180 00 Prague 8, Czech Republic.
ACS Omega. 2018 Sep 25;3(9):11865-11873. doi: 10.1021/acsomega.8b01811. eCollection 2018 Sep 30.
Poly(-isopropylacrylamide) (PNIPAM) is an important polymer with stimuli-responsive properties, making it suitable for various uses. Phase behavior of the temperature-sensitive PNIPAM polymer in the presence of four low-molecular weight additives -butylamine (-BuAM), -butyl alcohol (-BuOH), -butyl methyl ether (-BuME), and -butyl methyl ketone (-BuMK) was studied in water (DO) using high-resolution nuclear magnetic resonance (NMR) spectroscopy and dynamic light scattering. Phase separation was thermodynamically modeled as a two-state process which resulted in a simple curve which can be used for fitting of NMR data and obtaining all important thermodynamic parameters using simple formulas presented in this paper. The model is based on a modified van't Hoff equation. Phase separation temperatures and thermodynamic parameters (enthalpy and entropy change) connected with the phase separation of PNIPAM were obtained using this method. It was determined that is dependent on additives in the following order: (-BuAM) > (-BuOH) > (-BuME) > (-BuMK). Also, either increasing the additive concentration or increasing p of the additive leads to depression of . Time-resolved H NMR spin-spin relaxation experiments ( ) performed above the phase separation temperature of PNIPAM revealed high colloidal stability of the phase-separated polymer induced by the additives (relative to the neat PNIPAM/DO system). Small quantities of selected suitable additives can be used to optimize the properties of PNIPAM preparations including their phase separation temperatures, colloidal stabilities, and morphologies, thus improving the prospects for the application.
聚(N-异丙基丙烯酰胺)(PNIPAM)是一种具有刺激响应特性的重要聚合物,适用于多种用途。利用高分辨率核磁共振(NMR)光谱和动态光散射研究了温度敏感型PNIPAM聚合物在四种低分子量添加剂——丁胺(-BuAM)、丁醇(-BuOH)、丁基甲基醚(-BuME)和丁基甲基酮(-BuMK)存在下于水中(DO)的相行为。相分离被热力学建模为一个双态过程,得到一条简单曲线,该曲线可用于拟合NMR数据,并使用本文给出的简单公式获得所有重要的热力学参数。该模型基于修正的范特霍夫方程。使用此方法获得了与PNIPAM相分离相关的相分离温度以及热力学参数(焓变和熵变)。确定 依赖于添加剂的顺序如下: (-BuAM)> (-BuOH)> (-BuME)> (-BuMK)。此外,增加添加剂浓度或提高添加剂的p值都会导致 降低。在PNIPAM相分离温度以上进行的时间分辨H NMR自旋-自旋弛豫实验( )表明,添加剂诱导的相分离聚合物具有高胶体稳定性(相对于纯PNIPAM/DO体系)。少量选定的合适添加剂可用于优化PNIPAM制剂的性能,包括其相分离温度、胶体稳定性和形态,从而改善应用前景。