Kang Hongmei, Peng Baoliang, Liang Yanyan, Han Xia, Liu Honglai
Lab for Advanced Materials and Department of Chemistry, East China University of Science & Technology, Shanghai 200237, China.
J Colloid Interface Sci. 2009 May 1;333(1):135-40. doi: 10.1016/j.jcis.2008.12.072. Epub 2009 Feb 12.
The interactions between negatively charged diblock polyelectrolyte PDMA(71)-b-PAA(59) and oppositely charged gemini surfactant hexylene-1,6-bis(dodecyldimethylammonium bromide) (12-6-12) in basic media were studied using dynamic light scattering, fluorescence spectroscopy, surface tension, and (1)H NMR. With increased addition of surfactant, the conformation of polyelectrolyte experienced changes from the initial unimer with open-extended PAA block, to the nano-scaled aggregates/complexes with a maximum hydrodynamic diameter (D(h)), and finally to the stable complexes with a smaller D(h). Accordingly, the value of D(h) during the whole process of increasing the surfactant concentration changed from 14-17 nm, to 184 nm, and to the final 70 nm, respectively. This transformation was driven by the electrostatic attractive/repulsive interactions, the hydrophobic interaction between hydrophobic surfactant tails, and the hydrophilicity of PDMA block.
利用动态光散射、荧光光谱、表面张力和核磁共振氢谱(¹H NMR)研究了带负电荷的二嵌段聚电解质PDMA(71)-b-PAA(59)与带相反电荷的双子表面活性剂己二烯-1,6-双(十二烷基二甲基溴化铵)(12-6-12)在碱性介质中的相互作用。随着表面活性剂添加量的增加,聚电解质的构象经历了从初始具有开放伸展PAA嵌段的单分子,到具有最大流体力学直径(D(h))的纳米级聚集体/复合物,最终到具有较小D(h)的稳定复合物的变化。相应地,在增加表面活性剂浓度的整个过程中,D(h)的值分别从14 - 17纳米变为184纳米,最终变为70纳米。这种转变是由静电吸引/排斥相互作用、疏水表面活性剂尾部之间的疏水相互作用以及PDMA嵌段的亲水性驱动的。