Dopierala Katarzyna, Luczynski Jacek, Prochaska Krystyna
Institute of Chemical Engineering and Technology, Poznan University of Technology, Pl. M. Sklodowskiej-Curie 2, 60-965 Poznan, Poland.
Adv Colloid Interface Sci. 2009 Oct 30;151(1-2):49-56. doi: 10.1016/j.cis.2009.07.006. Epub 2009 Aug 6.
Equilibrium adsorption at the air/water interface of cationic surfactants belonging in the group of quaternary ammonium bromides was studied. Quaternary ammonium salts, derivatives of lysosomotropic substances with different alkyl chain numbers and hydrophobicities were investigated. Surface properties of considered compounds, were examined and presented against other quaternary ammonium bromides of different chemical structure and with different number of alkyl chains in the molecule. The Frumkin equation and reorientation model were used for a quantitative description of the process of their adsorption. It was found that considered biologically active derivatives reveal strong surface activity. Chemical structure-surface activity relationship was analyzed and referenced to biological activity. Symmetry of the molecules resulting from the number of alkyl chains is the factor determining the behavior of the surfactants at the air/water interface as well as in the bulk. Surfactants with asymmetrical structure show a strong tendency to reorientation, in opposite to tetraalkylammonium bromides and double chain surfactants. Furthermore, the role of ester bond was emphasized.
研究了季铵溴化物类阳离子表面活性剂在空气/水界面的平衡吸附。研究了具有不同烷基链数和疏水性的溶酶体亲和性物质衍生物季铵盐。考察了所考虑化合物的表面性质,并与具有不同化学结构和分子中不同烷基链数的其他季铵溴化物进行了对比。使用弗鲁姆金方程和重取向模型对其吸附过程进行定量描述。发现所考虑的生物活性衍生物具有很强的表面活性。分析了化学结构-表面活性关系,并参考了生物活性。由烷基链数量产生的分子对称性是决定表面活性剂在空气/水界面以及本体相中行为的因素。与四烷基溴化铵和双链表面活性剂相反,具有不对称结构的表面活性剂表现出很强的重取向倾向。此外,强调了酯键的作用。