Alila Sabrine, Boufi Sami, Belgacem Mohamed Naceur, Beneventi Davide
LMSE, Faculté des Sciences de Sfax, BP 802-3018, Sfax, Tunisia.
Langmuir. 2005 Aug 30;21(18):8106-13. doi: 10.1021/la050367n.
The adsorption of four cationic surfactants with different alkyl chain lengths on cellulose substrates was investigated. Cellulose fibers were used as model substrates, and primary alcohol groups of cellulose glycosyl units were oxidized into carboxylic groups to obtain substrates with different surface charges. The amount of surfactant adsorbed on the fiber surface, the fiber zeta-potential, and the amount of surfactant counterions (Cl(-)) released into solution were measured as a function of the surfactant bulk concentration, its molecular structure, the substrate surface charge, and the ionic strength. The contribution of each of these parameters to the shape of the adsorption isotherms was used to verify if surfactant adsorption and self-assembly models usually used to describe the behavior of surfactant/oxide systems can be applied, and with which limitations, to describe cationic surfactant adsorption onto oppositely charged cellulose substrates.
研究了四种不同烷基链长度的阳离子表面活性剂在纤维素底物上的吸附情况。以纤维素纤维作为模型底物,将纤维素糖基单元的伯醇基团氧化成羧基,从而获得具有不同表面电荷的底物。测量了吸附在纤维表面的表面活性剂的量、纤维的ζ电位以及释放到溶液中的表面活性剂抗衡离子(Cl(-))的量,这些都是表面活性剂本体浓度、其分子结构、底物表面电荷和离子强度的函数。利用这些参数对吸附等温线形状的贡献,来验证通常用于描述表面活性剂/氧化物体系行为的表面活性剂吸附和自组装模型是否可以应用于描述阳离子表面活性剂在带相反电荷的纤维素底物上的吸附,以及存在哪些局限性。