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Study of the interaction between a diblock polyelectrolyte PDMA-b-PAA and a gemini surfactant 12-6-12 in basic media

机译:在碱性介质中双嵌段聚电解质PDMA-b-PAA与双子表面活性剂12-6-12之间相互作用的研究

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摘要

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 ~1H 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.
机译:使用动态光散射研究了碱性介质中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烯-1,6-双(十二烷基二甲基溴化铵)(12-6-12)之间的相互作用,荧光光谱,表面张力和〜1H NMR。随着表面活性剂添加量的增加,聚电解质的构象经历了变化,从最初的开放式PAA嵌段单体到具有最大流体动力学直径(D_h)的纳米级聚集体/复合物,最后变为具有较小D_h的稳定复合物。 。因此,在增加表面活性剂浓度的整个过程中,D_h的值分别从14-17nm变化为184nm,并最终变化为70nm。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。

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