Hill Christopher, Umetsu Yasushi, Fujita Kazuki, Endo Takumi, Sato Kodai, Yoshizawa Atsushi, Rogers Sarah E, Eastoe Julian, Sagisaka Masanobu
School of Chemistry, University of Bristol, Cantock's Close, Bristol BS8 1TS, United Kingdom.
Department of Frontier Materials Chemistry, Graduate School of Science and Technology, Hirosaki University, 3 Bunkyo-cho, Hirosaki, Aomori 036-8561, Japan.
Langmuir. 2020 Dec 8;36(48):14829-14840. doi: 10.1021/acs.langmuir.0c02835. Epub 2020 Nov 23.
The interfacial properties and water-in-CO (W/CO) microemulsion (μE) formation with double- and novel triple-tail surfactants bearing trimethylsilyl (TMS) groups in the tails are investigated. Comparisons of these properties are made with those for analogous hydrocarbon (HC) and fluorocarbon (FC) tail surfactants. Surface tension measurements allowed for critical micelle concentrations (CMC) and surface tensions at the CMC (γ) to be determined, resulting in the following trend in surface activity FC > TMS > HC. Addition of a third surfactant tail gave rise to increased surface activity, and very low γ values were recorded for the double/triple-tail TMS and HC surfactants. Comparing effective tail group densities (ρ) of the respective surfactants allowed for an understanding of how γ is affected by both the number of surfactant tails and the chemistry of the tails. These results highlight the important role of tail group chemical structure on ρ for double-tail surfactants. For triple-tail surfactants, however, the degree to which ρ is affected by tail group architecture is harder to discern due to formation of highly dense layers. Stable W/CO μEs were formed by both the double- and the triple-tail TMS surfactants. High-pressure small-angle neutron scattering (HP-SANS) has been used to characterize the nanostructures of W/CO μEs formed by the double- and triple-tail surfactants, and at constant pressure and temperature, the aqueous cores of the microemulsions were found to swell with increasing water-to-surfactant ratio (). A maximum value of 25 was recorded for the triple-tail TMS surfactant, which is very rare for nonfluorinated surfactants. These data therefore highlight important parameters required to design fluorine-free environmentally responsible surfactants for stabilizing W/CO μEs.
研究了带有三甲基硅烷基(TMS)基团的双尾和新型三尾表面活性剂的界面性质以及水包CO(W/CO)微乳液(μE)的形成。将这些性质与类似的烃类(HC)和氟碳类(FC)尾链表面活性剂的性质进行了比较。通过表面张力测量确定了临界胶束浓度(CMC)和CMC时的表面张力(γ),得出表面活性的如下趋势:FC>TMS>HC。添加第三条表面活性剂尾链会提高表面活性,对于双尾/三尾TMS和HC表面活性剂,记录到非常低的γ值。比较各表面活性剂的有效尾链基团密度(ρ),有助于理解γ如何受到表面活性剂尾链数量和尾链化学性质的影响。这些结果突出了尾链基团化学结构对双尾表面活性剂ρ的重要作用。然而,对于三尾表面活性剂,由于形成了高密度层,ρ受尾链基团结构影响的程度较难辨别。双尾和三尾TMS表面活性剂均形成了稳定的W/CO μE。高压小角中子散射(HP-SANS)已用于表征由双尾和三尾表面活性剂形成的W/CO μE的纳米结构,在恒定压力和温度下,发现微乳液的水核随着水与表面活性剂比率()的增加而膨胀。对于三尾TMS表面活性剂,记录到的最大值为25,这对于非氟化表面活性剂来说非常罕见。因此,这些数据突出了设计用于稳定W/CO μE的无氟环保型表面活性剂所需的重要参数。