School of Chemical Engineering, Purdue University, 480 Stadium Mall Dr., West Lafayette, IN 47907, United States.
J Colloid Interface Sci. 2013 Dec 1;411:265-72. doi: 10.1016/j.jcis.2013.05.048. Epub 2013 Jun 14.
Atomic force microscopy (AFM) was used to investigate the effect of relative humidity (RH) on the adhesion forces between silicon nitride AFM probes, hydrophilic stainless steel, and hydrophobic Perspex® (polymethylmethacrylate, PMMA). In addition, AFM-based phase contrast imaging was used to quantify the amount and location of adsorbed water present on these substrates at RH levels ranging from 15% to 65% at 22°C. Both the adhesion forces and the quantities of adsorbed moisture were seen to vary with RH, and the nature of this variation depended on the hydrophobicity of the substrate. For the Perspex®, both the adhesion force and the amount of adsorbed moisture were essentially independent of RH. For the stainless steel substrate, adsorbed moisture increased continuously with increasing RH, while the adhesion force rose from a minimum at 15% RH to a broad maximum between 25% and 35% RH. From 35% to 55% RH, the adhesion force dropped continuously to an intermediate level before rising again as 65% RH was approached. The changes in adhesion force with increasing relative humidity in the case of the stainless steel substrate were attributed to a balance of effects associated with adsorbed, sub-continuum water on the cantilever and steel. Hydrogen bonding interactions between these adsorbed water molecules were thought to increase the adhesion force. However, when significant quantities of molecular water adsorbed, these molecules were expect to decrease adhesion by screening the van der Waals interactions between the steel and the cantilever tip, and by increasing the separation distance between these solid surfaces when they were 'in contact'. Finally, the slight increase in adhesion between 55% and 65% RH was attributed to true capillary forces exerted by continuum water on the two solid surfaces.
原子力显微镜(AFM)被用于研究相对湿度(RH)对氮化硅 AFM 探针、亲水不锈钢和疏水 Perspex®(聚甲基丙烯酸甲酯,PMMA)之间粘附力的影响。此外,还使用基于 AFM 的相差成像来定量测量在 22°C 下 RH 范围为 15%至 65%时这些基底上吸附水的量和位置。粘附力和吸附水分的量都随 RH 而变化,这种变化的性质取决于基底的疏水性。对于 Perspex®,粘附力和吸附水分的量基本上与 RH 无关。对于不锈钢基底,吸附水分随 RH 的增加而连续增加,而粘附力则从 15% RH 的最小值上升到 25%至 35% RH 之间的宽最大值。从 35%到 55% RH,粘附力连续下降到中间水平,然后在接近 65% RH 时再次上升。不锈钢基底的粘附力随相对湿度增加而变化归因于与悬臂和钢上吸附的亚连续水相关的平衡效应。这些吸附水分子之间的氢键相互作用被认为增加了粘附力。然而,当吸附大量的分子水时,这些分子通过屏蔽钢和悬臂尖端之间的范德华相互作用以及当它们“接触”时增加这些固体表面之间的分离距离,从而降低了粘附力。最后,55%至 65% RH 之间粘附力的轻微增加归因于连续水上对两个固体表面施加的微小毛细力。