Lamch Łukasz, Leszczyńska Izabella, Długowska Daria, Szczęsna-Górniak Weronika, Batys Piotr, Jarek Ewelina, Wilk Kazimiera A, Warszyński Piotr
Department of Organic and Pharmaceutical Technology, Faculty of Chemistry, Wrocław University of Science and Technology, Wybrzeże Wyspiańskiego 27, Wrocław 50-370, Poland.
Jerzy Haber Institute of Catalysis and Surface Chemistry, Polish Academy of Sciences, Niezapominajek 8, Kraków 30-239, Poland.
Langmuir. 2025 Apr 1;41(12):8125-8137. doi: 10.1021/acs.langmuir.4c04803. Epub 2025 Mar 21.
The interfacial behavior of aqueous solutions of newly synthesized 2-alkyl-,,,',','-hexamethylpropan-1,3-ammonium dibromides with decyl, dodecyl, and tetradecyl alkyl chains was investigated both experimentally and theoretically. The results of the surface tension measurements were described using the modified surface quasi-two-dimensional electrolyte (mSTDE) model of ionic surfactant adsorption, which was supported by molecular dynamics simulations. Our contribution encompasses the design, synthesis, and characterization of a novel class of dicephalic-type cationic surfactants, branched on a methine motif, possessing two symmetric trimethylammonium groups, which constitute a double-head extension of the standard alkyltrimethylammonium salts of the single-head, single-tail structure. The convenient synthetic route and final purification steps allowed for the high-yield, high-purity production of the surfactants. Dicephalic-type surfactants demonstrated lower surface activity and higher critical micelle concentration values when compared with their single head-single tail counterparts. That can be attributed primarily to the presence of strong electrostatic repulsive forces within the bulky, double-charge headgroups and significant counterion condensation. Furthermore, molecular dynamics simulations demonstrated a propensity for the desorption of surfactants from the interface, even in diluted solutions, which constrained the attainable surface concentration and resulted in a lower reduction in surface tension. The mSTDE model of adsorption provided an excellent description of the experimental surface isotherms with a concise set of parameters. The model's predictive power was demonstrated by the studies of the effect of inorganic salts on the surface activity of investigated surfactants. Our unique approach enabled us to gain a theoretical explanation of the newly devised surfactants' behavior at the water/air interface.
对新合成的具有癸基、十二烷基和十四烷基链的2-烷基-,,,',','-六甲基丙烷-1,3-二溴化铵水溶液的界面行为进行了实验和理论研究。使用离子表面活性剂吸附的改进表面准二维电解质(mSTDE)模型描述了表面张力测量结果,该模型得到了分子动力学模拟的支持。我们的贡献包括设计、合成和表征一类新型的双头部型阳离子表面活性剂,其在次甲基基序上分支,具有两个对称的三甲基铵基团,构成了单头单尾结构的标准烷基三甲基铵盐的双头延伸。便捷的合成路线和最终的纯化步骤使得能够高产率、高纯度地生产表面活性剂。与单头单尾的对应物相比,双头部型表面活性剂表现出较低的表面活性和较高的临界胶束浓度值。这主要可归因于庞大的双电荷头基内存在强静电排斥力以及显著的反离子凝聚。此外,分子动力学模拟表明,即使在稀释溶液中,表面活性剂也有从界面解吸的倾向,这限制了可达到的表面浓度,并导致表面张力降低幅度较小。吸附的mSTDE模型用一组简洁的参数对实验表面等温线进行了出色的描述。通过研究无机盐对所研究表面活性剂表面活性的影响,证明了该模型的预测能力。我们独特的方法使我们能够对新设计的表面活性剂在水/空气界面的行为获得理论解释。