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十六烷基三甲基溴化铵与 Triton X - 100 混合物水溶液对聚四氟乙烯的润湿性

The wettability of polytetrafluoroethylene by aqueous solution of cetyltrimethylammonium bromide and Triton X-100 mixtures.

作者信息

Szymczyk Katarzyna, Jańczuk Bronisław

机构信息

Department of Interfacial Phenomena, Faculty of Chemistry, Maria Curie-Skłodowska University, Maria Curie-Skłodowska Sq. 3, 20-031 Lublin, Poland.

出版信息

J Colloid Interface Sci. 2006 Nov 1;303(1):319-25. doi: 10.1016/j.jcis.2006.07.058. Epub 2006 Jul 27.

Abstract

Measurements of the advancing contact angle (theta) were carried out for aqueous solution of cetyltrimethylammonium bromide (CTAB) and p-(1,1,3,3-tetramethylbutyl) phenoxypoly(ethylene glycol), Triton X-100 (TX100) mixtures on polytetrafluoroethylene (PTFE). The obtained results indicate that the wettability of PTFE depends on the concentration and composition of the surfactants mixture. There is a minimum of the dependence between contact angle and composition of the mixtures for PTFE for each concentration at a monomer mole fraction of CTAB, alpha, equal 0.2, which points to the synergism in the wettability of PTFE. In contrast to Zisman, there is no linear dependence between costheta and the surface tension of aqueous solution of CTAB and TX100 mixtures for all studied systems, but a linear dependence exists between the adhesional tension and surface tension for PTFE in the whole concentration range, the slope of which is -1, that suggests that the surface excess of the surfactant concentration at the PTFE-solution interface is the same as that at the solution-air interface for a given bulk concentration. It was also found that the work of adhesion of aqueous solution of surfactants to PTFE surface did not depend on the type of surfactant and its concentration. It means that the interactions across PTFE-solution interface were constant for the systems studied, and they were largely Lifshitz-van de Waals type. On the basis of the surface tension of PTFE and the Young equation and thermodynamic analysis of the adhesion work of aqueous solution of surfactant to the polymer surface it was found that in the case of PTFE the changes of the contact angle as a function of the mixture of nonionic and cationic surfactants concentration resulted only from changes of the polar component of solution surface tension.

摘要

对十六烷基三甲基溴化铵(CTAB)和对(1,1,3,3 - 四甲基丁基)苯氧基聚(乙二醇)(Triton X - 100,TX100)混合物的水溶液在聚四氟乙烯(PTFE)上进行了前进接触角(θ)的测量。所得结果表明,PTFE的润湿性取决于表面活性剂混合物的浓度和组成。对于每种浓度的混合物,在CTAB的单体摩尔分数α等于0.2时,PTFE的接触角与混合物组成之间的依赖关系存在最小值,这表明PTFE润湿性存在协同作用。与齐斯曼理论不同的是,对于所有研究体系,cosθ与CTAB和TX100混合物水溶液的表面张力之间不存在线性关系,但在整个浓度范围内,PTFE的粘附张力与表面张力之间存在线性关系,其斜率为 - 1,这表明在给定本体浓度下,PTFE - 溶液界面处表面活性剂浓度的表面过剩与溶液 - 空气界面处相同。还发现表面活性剂水溶液对PTFE表面的粘附功不取决于表面活性剂的类型及其浓度。这意味着对于所研究的体系,PTFE - 溶液界面间的相互作用是恒定的,且主要是利夫希茨 - 范德华类型。基于PTFE的表面张力、杨氏方程以及表面活性剂水溶液对聚合物表面粘附功的热力学分析发现,对于PTFE,接触角随非离子和阳离子表面活性剂混合物浓度的变化仅源于溶液表面张力极性成分的变化。

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