Girase Mayursing, Patel Panchami, Ghosh Arup Kumar, Thareja Prachi, Mata Jitendra, Kuperkar Ketan, Bahadur Pratap
Department of Chemistry, Sardar Vallabhbhai National Institute of Technology (SVNIT), Surat 395 007, Gujarat, India.
Department of Chemical Engineering, Indian Institute of Technology (IIT), Gandhinagar 382 355, Gujarat, India.
Langmuir. 2025 Sep 30;41(38):26516-26530. doi: 10.1021/acs.langmuir.5c04401. Epub 2025 Sep 15.
This study uniquely reveals the hierarchical self-assembly and complex micellar transitions in a selective zwitterionic-anionic mix surfactant system in aqueous solution and the presence of varied salts. A combination of tensiometry, rheology, and small-angle neutron scattering (SANS) experiments was used to investigate these nanoscale transitions in a selective mixed micellar system. The critical micelle concentration (CMC) for single and mixed systems was determined at ambient temperature, and the interaction parameter (β), depicting favorable synergism at a specific mole fraction, was calculated using Rubingh's regular solution theory (RST). Again, various thermodynamic parameters, such as Maeda's free energy of micellization (Δ), the free energy of micellization (Δ), and the free energy of adsorption (Δ), were calculated. Density functional theory (DFT) calculations were carried out employing the Gaussian 09W software package and visualized using Gauss View 6.0, which yielded varied quantum chemical descriptors that supported the marked influence of the anionic surfactant in favoring the micellization of the zwitterionic surfactant in the examined system. Also, the obtained reduced density gradient (RDG) and noncovalent interactions (NCI) enabled the understanding of the synergistic interactions involved therein, which is affirmed by Two-Dimensional Nuclear Overhauser Enhancement Spectroscopy (2D-NOESY) that explored the self-assembly mechanism in the examined micellar solution. The rheological parameters, such as the modulus of elasticity (') and modulus of viscosity (″), described varied solution behavior covering fluidic, viscous, and gel formation, thus attributing viscoelasticity, particularly in the presence of salts. The SANS approach inferred micellar growth with various morphology transitions ranging from spheres, ellipsoids, and cylinders. Interestingly, it also displayed a fractal dimension () in the examined system, not previously reported for this class of surfactant mixtures, making this study very novel, giving an account of the specific binding of anions and cations from the added electrolyte.
本研究独特地揭示了在水溶液中选择性两性离子 - 阴离子混合表面活性剂体系以及不同盐存在下的分级自组装和复杂的胶束转变。采用表面张力测定、流变学和小角中子散射(SANS)实验相结合的方法,研究了选择性混合胶束体系中的这些纳米级转变。在环境温度下测定了单一和混合体系的临界胶束浓度(CMC),并使用鲁宾的正规溶液理论(RST)计算了描述特定摩尔分数下有利协同作用的相互作用参数(β)。此外,还计算了各种热力学参数,如前田的胶束化自由能(Δ)、胶束化自由能(Δ)和吸附自由能(Δ)。使用高斯09W软件包进行密度泛函理论(DFT)计算,并使用高斯视图6.0进行可视化,得到了各种量子化学描述符,支持了阴离子表面活性剂对所研究体系中两性离子表面活性剂胶束化的显著影响。此外,获得的约化密度梯度(RDG)和非共价相互作用(NCI)有助于理解其中涉及的协同相互作用,这一点通过二维核Overhauser增强光谱(2D - NOESY)得到了证实,该光谱探索了所研究胶束溶液中的自组装机制。流变学参数,如弹性模量(')和粘度模量(″),描述了涵盖流体、粘性和凝胶形成的不同溶液行为,从而归因于粘弹性,特别是在有盐存在的情况下。SANS方法推断出胶束生长以及从球体、椭球体和圆柱体等各种形态转变。有趣的是,它还在所研究的体系中显示出分形维数(),此前这类表面活性剂混合物未曾有过报道,这使得本研究非常新颖,阐述了添加电解质中阴离子和阳离子的特异性结合。