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首页> 外文期刊>Langmuir: The ACS Journal of Surfaces and Colloids >Measurements of the force between fluorocarbon monolayer surfaces in air and water
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Measurements of the force between fluorocarbon monolayer surfaces in air and water

机译:空气和水中的碳氟化合物单层表面之间的力的测量

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摘要

We have measured forces between fluorocarbon surfaces prepared by three different methods using heptadecafluoro-1,1,2,2,-tetrahydrodecyltriethoxysilane (FTE): LB deposition (LB), adsorption from diluted FTE solution with chloroform (FTE/CHCl3), and adsorption from undiluted FTE liquid (FTEeat). In dry air, a van der Waals attraction was observed between the surfaces except for the FTEeat surfaces. The Hamaker constant was found to be 7 x 10(-20) J, which is comparable to that of the fused silica substrate. In saturated water vapor, a capillary bridging force was observed with FTE/CHCl3 and FTEeat owing to the adsorption of water between the substrate and the fluorocarbon layer while a van der Waals attraction identical to that observed in dry air was detected between the LB surfaces. Only the LB surfaces were stable enough to effectively partition the adsorbed water layer beneath the fluorocarbon layer and air. In water, long-range forces from 120 to 150 nm were observed with FTEeat while a rather shorter-range attraction within 40 nm was observed with LB and FTE//CHCl3. The change in force profile with time could be explained by a change in surface properties occurring on immersion in water. It is suggested that the greater the number of mobile molecules, the longer-range the attraction observed between the surfaces. On the LB surfaces, after unbound molecules were removed, the force profile did not change for at least 5 days and a strong attractive force at separations below 12-13 nm was observed in water. The range of this force is in agreement with other studies showing only a comparatively short-range attraction between stable and homogeneous hydrophobic surfaces. The magnitude of the attraction is close to that of the short-range force measured previously between mica surfaces coated with fluorocarbon surfactant monolayers. This suggests that the strong, short-range attraction measured between many LB surfaces is related to the force between stable hydrophobic surfaces but that the very long-range exponentially decaying force has a different origin. [References: 44]
机译:我们测量了使用三种不同方法使用七氟1,1,2,2,-四氢癸基三乙氧基硅烷(FTE)制备的碳氟化合物表面之间的力:LB沉积(LB),用氯仿稀释的FTE溶液的吸附(FTE / CHCl3)和吸附来自未稀释的FTE液体(FTE /纯净)。在干燥的空气中,除FTE /净表面外,在表面之间均观察到范德华吸引力。发现Hamaker常数为7 x 10(-20)J,与熔融石英基底的常数相当。在饱和水蒸气中,由于水在基质和碳氟化合物层之间的吸附,因此观察到FTE / CHCl3和FTE /纯的毛细管桥连力,而在LB之间检测到的范德华吸引力与干燥空气相同表面。仅LB表面足够稳定以有效地将碳氟化合物层下面的吸附水层和空气分隔开。在水中,使用FTE /纯净溶液可观察到120至150 nm的远距离力,而使用LB和FTE // CHCl3则可在40 nm范围内观察到较短的吸引力。力分布随时间的变化可以用浸入水中时表面性质的变化来解释。建议的是,可移动分子的数量越多,在表面之间观察到的吸引力越长。在LB表面上,除去未结合的分子后,力曲线至少5天没有变化,并且在水中低于12-13 nm的分离处观察到了很强的吸引力。该力的范围与其他研究一致,表明稳定和均质的疏水表面之间只有相对短程的吸引力。吸引力的大小接近于先前在涂有碳氟化合物表面活性剂单层的云母表面之间测得的短程力的大小。这表明,在许多LB表面之间测得的强而短距离的吸引力与稳定的疏水表面之间的力有关,但非常长的指数衰减力的来源却不同。 [参考:44]

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