Szymczyk Katarzyna, Jańczuk Bronisław
Department of Interfacial Phenomena, Faculty of Chemistry, Maria Curie-Skłodowska University, Maria Curie-Skłodowska Sq. 3, 20-031 Lublin, Poland.
Langmuir. 2008 Aug 5;24(15):7755-60. doi: 10.1021/la8008078. Epub 2008 Jun 24.
Measurements of the advancing contact angle (theta) were carried out for aqueous solution of p-(1,1,3,3-tetramethylbutyl)phenoxypoly(ethylene glycol), Triton X-100 (TX100), and Triton X-165 (TX165) mixtures on glass. The obtained results indicate that the wettability of glass depends on the concentration and composition of the surfactant mixture. The relationship between the contact angle and concentration suggests that the lowest wettability corresponds to the concentration of TX100 and TX165 and their mixture near the critical micelle concentration (CMC). The minimum of the dependence between the contact angle and composition of the mixtures for each concentration at a monomer mole fraction of TX100, alpha, equals 0.2 and 0.4 points to synergism in the wettability of the glass surface. In contrast to the results of Zisman ( Zisman, W. A. In Contact Angle, Wettability and Adhesion; Gould, R. F., Ed.; Advances in Chemistry Series 43; American Chemical Society Washington, DC, 1964; p 1 ) there was no linear dependence between cos theta and the surface tension of aqueous solutions of TX100 and TX165 mixtures for all studied systems, but a linear dependence exists between the adhesional tension and surface tension for glass, practically, in the whole concentration range of surfactants studied, the slopes of which are positive in the range of 0.43-0.67. These positive slopes indicate that the interactions between the water molecules and glass surface might be stronger than those between the surface and surfactant molecules. So, the surface excess of surfactant concentration at the glass-water interface is probably negative, and the possibility for surfactant to adsorb at the glass/water film-water interface is higher than that at the glass-water interface. This conclusion is confirmed by the values of the work of adhesion of "pure" surfactants, aqueous solutions of surfactants, and aqueous solutions of their mixtures to the glass surface and by the negative values of glass-water interfacial tension determined from the Young equation in the range of surfactant concentrations corresponding to their unsaturated monolayer at the water-air interface.
对玻璃表面上对 -(1,1,3,3 - 四甲基丁基)苯氧基聚(乙二醇)、吐温X - 100(TX100)和吐温X - 165(TX165)混合物的水溶液进行了前进接触角(θ)的测量。所得结果表明,玻璃的润湿性取决于表面活性剂混合物的浓度和组成。接触角与浓度之间的关系表明,最低润湿性对应于TX100和TX165及其混合物接近临界胶束浓度(CMC)时的浓度。在TX100的单体摩尔分数α等于0.2和0.4时,每种浓度下接触角与混合物组成之间的依赖关系最小值表明玻璃表面润湿性存在协同作用。与齐斯曼(Zisman, W. A.《接触角、润湿性和粘附力》;Gould, R. F.编;《化学进展系列》43;美国化学学会,华盛顿特区,1964;第1页)的结果相反,对于所有研究体系,TX100和TX165混合物水溶液的cosθ与表面张力之间不存在线性关系,但对于玻璃,粘附张力与表面张力之间存在线性关系,实际上,在所研究的表面活性剂整个浓度范围内均如此,其斜率在0.43 - 0.67范围内为正值。这些正斜率表明水分子与玻璃表面之间的相互作用可能比表面与表面活性剂分子之间的相互作用更强。因此,玻璃 - 水界面处表面活性剂浓度的表面过剩可能为负,表面活性剂在玻璃/水 - 膜 - 水界面吸附的可能性高于在玻璃 - 水界面吸附的可能性。这一结论通过“纯”表面活性剂、表面活性剂水溶液及其混合物与玻璃表面的粘附功值以及在对应于水 - 空气界面不饱和单分子层的表面活性剂浓度范围内由杨氏方程确定的玻璃 - 水界面张力的负值得到证实。