首页> 外文OA文献 >Dynamic Surface Tension Behaviour in a Photoresponsive Surfactant System
【2h】

Dynamic Surface Tension Behaviour in a Photoresponsive Surfactant System

机译:光响应表面活性剂体系中的动态表面张力行为

摘要

We report on the surface properties of a photoresponsive surfactant that incorporates the light-sensitive azobenzene group into its tail. Cis-trans photo-isomerization of this group alters the ability of the surfactant to pack into adsorbed monolayers at an air-water interface or into aggregates in solution, causing a significant variation in bulk and surface properties upon changes in the illumination conditions. NMR studies indicate that a solution left in the dark for an extended period of time contains trans isomer almost exclusively, while samples exposed to light of fixed wavelength eventually reach a photostationary equilibrium with significant amounts of both isomers present. Dynamic surface tension studies performed on this system under different illumination conditions (dark, UV light, visible light) show profoundly different approaches to equilibrium. At concentrations well above the CMC, the same equilibrium tension is reached in all three cases, presumably corresponding to a surface saturated with the trans (more surface active) isomer. The dark sample shows a simple, single-step relaxation in surface tension after creation of a fresh interface, while the UV and visible samples exhibit a more rapid initial decrease in tension, followed by a plateau of nearly constant tension, and end with a final relaxation to equilibrium. It is hypothesized that this behavior of the UV and visible samples is caused by competitive adsorption between the cis and trans isomers present in these mixtures. Presumably the cis surfactant reaches the interface more quickly, leading to a cis-dominated interface having a tension value corresponding to the intermediate plateau, but is ultimately displaced by the trans isomer. Diffusional time scale arguments which consider the extremes of possible micellar dissolution rates are used to analyze the relaxation data of the dark sample, and the results indicate that micellar dissolution in these samples is slow.
机译:我们报告了将光敏偶氮苯基掺入其尾部的光敏表面活性剂的表面性能。该基团的顺-反光异构化改变了表面活性剂在空气-水界面处堆积成吸附的单分子层或溶液中聚集体的能力,从而在光照条件变化时引起体积和表面性质的显着变化。 NMR研究表明,在黑暗中长时间放置的溶液几乎只包含反式异构体,而暴露于固定波长的光的样品最终会达到光平稳平衡,并且存在大量的两种异构体。在不同照明条件下(暗,紫外光,可见光)在此系统上进行的动态表面张力研究表明,实现平衡的方法截然不同。在远高于CMC的浓度下,在所有三种情况下均达到相同的平衡张力,大概对应于被反式(更具表面活性)异构体饱和的表面。深色样品在创建新界面后显示出表面张力的简单,单步松弛,而紫外线和可见光样品则显示出较快的初始张力降低,随后出现了几乎恒定的张力平稳状态,最后结束了松弛到平衡。据推测,紫外线和可见光样品的这种行为是由这些混合物中存在的顺式和反式异构体之间的竞争性吸附引起的。据推测,顺式表面活性剂更快地到达界面,从而导致具有与中间平台相对应的张力值的顺式为主的界面,但是最终被反式异构体置换。考虑可能的胶束溶解速率的极值的扩散时标论点用于分析深色样品的弛豫数据,结果表明这些样品中的胶束溶解较慢。

著录项

相似文献

  • 外文文献
  • 中文文献
  • 专利

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号