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十六烷基三甲基溴化铵和/或十六烷基二甲基苄基氯化铵在部分覆盖悬汞滴电极上的吸附。

Adsorption of cetyltrimethylammonium bromide and/or cetyldimethylbenzylammonium chloride on partly covered hanging mercury drop electrode.

机构信息

Laboratory of Physical Chemistry, Department of Chemistry, Aristotle University of Thessaloniki, 54124 Thessaloniki, Greece.

出版信息

J Colloid Interface Sci. 2011 Oct 1;362(1):164-71. doi: 10.1016/j.jcis.2011.06.026. Epub 2011 Jun 24.

DOI:10.1016/j.jcis.2011.06.026
PMID:21752392
Abstract

Adsorbed cetyldimethylbenzylammonium chloride (CDBACl) or cetyltrimethylammonium bromide (CTAB) on mercury is used as template for the adsorption of CTAB, CDBACl, or their equimolar mixture at 20 °C. Adsorptive stripping voltammetry with the two step procedure is used. The results are compared with previously published results on the adsorption of CTAB and CDBACl on mercury and then transferred in base electrolyte. A surfactant is preadsorbed. The adsorption of the second does not remove away from the mercury the first one, as evidenced by the capacitance measurements and the repeated scans. The surfactants were maintained close to each other and in the vicinity of the electrode by the applied electric field. In all cases studied, there was a decrease in the capacitance in the potential range -0.8 to -1 V to very low capacitance values forming condensed film. Mixed films and synergy effects were observed. The already adsorbed CTAB on mercury did not permit the desorption-reorientation peaks of CDBACl. Shifts of the capacitance peaks were observed to more positive potentials and were attributed to the occurrence of a slow change in the organization of the monolayer. The electrical state of the preadsorbed surfactant would be of critical importance in the formation of the various structures. The results suggested that the ordering and arrangement of molecules could be controlled by appropriate selection of templates.

摘要

吸附在汞上的十六烷基二甲基苄基氯化铵 (CDBACl) 或十六烷基三甲基溴化铵 (CTAB) 可用作在 20°C 下吸附 CTAB、CDBACl 或它们等摩尔混合物的模板。采用两步程序进行吸附溶出伏安法。将结果与之前在汞上吸附 CTAB 和 CDBACl 的发表结果进行比较,然后转移到基础电解质中。预先吸附表面活性剂。通过电容测量和重复扫描证明,第二个的吸附不会将第一个从汞上移开。通过施加的电场,表面活性剂彼此靠近并靠近电极。在所研究的所有情况下,在 -0.8 至 -1 V 的电位范围内电容都会降低,形成非常低的电容值,形成凝聚膜。观察到混合膜和协同效应。已经吸附在汞上的 CTAB 不允许 CDBACl 的解吸-重定向峰出现。观察到电容峰向更正的电位移动,这归因于单层组织的缓慢变化的发生。预吸附表面活性剂的电状态对于各种结构的形成具有至关重要的意义。结果表明,通过适当选择模板,可以控制分子的有序排列和排列。

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