Department of Pure and Applied Chemistry in Faculty of Science and Technology and Research Institute for Science and Technology, Tokyo University of Science, 2641 Yamazaki, Noda, Chiba 278-8510, Japan.
Langmuir. 2010 Nov 16;26(22):17119-25. doi: 10.1021/la1028367. Epub 2010 Sep 29.
The adsorption of the monomeric/gemini surfactant mixtures at the silica/aqueous solution interface has been characterized on the basis of quartz crystal microbalance with dissipation monitoring (QCM-D) and atomic force microscopy (AFM) data. The gemini surfactant employed in this study was cationic 1,2-bis(dodecyldimethylammonio)ethane dibromide (12-2-12). This surfactant was mixed with monomeric surfactants (dodecyltrimethylammonium bromide (DTAB), hexadecyltrimethylammonium bromide (HTAB), and octaoxyethylenedodecyl ether (C(12)EO(8))) in the presence of an added electrolyte (NaBr). The key finding in our current study is that the addition of the gemini surfactant (12-2-12) makes significant impact on the adsorption properties even when the mole fraction of 12-2-12 is quite low in the surfactant mixtures. This is suggested by the experimental results that (i) the QCM-D adsorption isotherms measured for the monomeric/gemini surfactant mixtures shift to the region of lower surfactant concentrations compared with the monomeric single systems; (ii) the adsorbed layer morphology largely depends on the mole fraction of 12-2-12 in the surfactant mixtures, and the increased 12-2-12 mole fraction results in the less curved surface aggregates; and (iii) the addition of 12-2-12 yields a relatively rigid adsorbed layer when compared with the layer formed by the monomeric single systems. These adsorption properties result from the fact that the more favorable interaction of 12-2-12 with the silica surface sites drives the overall surfactant adsorption in these mixtures, which is particularly obvious in the region of low surfactant concentrations and at the 12-2-12 low mole fractions. We believe that this knowledge should be important when considering the formulation of gemini surfactants into various chemical products.
基于石英晶体微天平耗散监测(QCM-D)和原子力显微镜(AFM)数据,研究了混合单体/双子表面活性剂在二氧化硅/水溶液界面的吸附特性。本研究中使用的双子表面活性剂为阳离子 1,2-双(十二烷基二甲基铵)乙烷二溴化物(12-2-12)。该表面活性剂与单体表面活性剂(十二烷基三甲基溴化铵(DTAB)、十六烷基三甲基溴化铵(HTAB)和辛氧基乙基十二醚(C(12)EO(8)))混合,并添加电解质(NaBr)。我们目前研究的关键发现是,即使双子表面活性剂(12-2-12)的摩尔分数在表面活性剂混合物中相当低,它的添加也会对吸附性质产生重大影响。这可以从以下实验结果得到证明:(i)与单体单体系相比,测量的单体/双子表面活性剂混合物的 QCM-D 吸附等温线向较低表面活性剂浓度区域移动;(ii)吸附层形态在很大程度上取决于表面活性剂混合物中 12-2-12 的摩尔分数,增加 12-2-12 的摩尔分数会导致表面聚集物的曲率减小;(iii)与单体单体系形成的层相比,添加 12-2-12 会产生相对刚性的吸附层。这些吸附性质是由于 12-2-12 与二氧化硅表面位点之间更有利的相互作用促使这些混合物中的整体表面活性剂吸附,这在低表面活性剂浓度区域和 12-2-12 低摩尔分数区域尤为明显。我们认为,当考虑将双子表面活性剂配方成各种化学产品时,这些知识应该很重要。