Nguyen Khoi T, Nguyen Tuan D, Nguyen Anh V
School of Chemical Engineering, The University of Queensland , Brisbane QLD 4072, Australia.
Langmuir. 2014 Jun 24;30(24):7047-51. doi: 10.1021/la500256a. Epub 2014 Jun 11.
Remarkable adsorption enhancement and packing of dilute mixtures of water-soluble oppositely-charged surfactants, sodium dodecyl sulfate (SDS) and dodecyl amine hydrochloride (DAH), at the air-water interface were observed by using sum frequency generation spectroscopy and tensiometry. The interfacial water structure was also observed to be significantly influenced by the SDS-DAH mixtures, differently from the synergy of the single surfactants. Most strikingly, the obtained spectroscopic evidence suggests that the interfacial hydrophobic alkyl chains of the binary mixtures assemble differently from those of single surfactants. This study highlights the significance of the cooperative interaction between the headgroups of oppositely charged binary surfactant systems and subsequently provides some insightful observations about the molecular structure of the air-aqueous interfacial water molecules and, more importantly, about the packing nature of the surfactant hydrophobic chains of dilute SDS-DAH mixtures of concentration below 1% of the CMC.
通过和频振动光谱法和表面张力测定法,观察到水溶性带相反电荷的表面活性剂十二烷基硫酸钠(SDS)和十二烷基胺盐酸盐(DAH)的稀混合物在气-水界面处具有显著的吸附增强和聚集现象。还观察到SDS-DAH混合物对界面水结构有显著影响,这与单一表面活性剂的协同作用不同。最引人注目的是,获得的光谱证据表明二元混合物的界面疏水烷基链的组装方式与单一表面活性剂不同。这项研究突出了带相反电荷的二元表面活性剂体系头基之间协同相互作用的重要性,随后提供了一些关于气-水界面水分子分子结构的深刻见解,更重要的是,提供了关于浓度低于临界胶束浓度(CMC)1%的稀SDS-DAH混合物中表面活性剂疏水链堆积性质的见解。