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Modification of surface interactions and friction by adsorbed dendrimers: 2. High surface-energy -OH-terminated carbosilane dendrimers

机译:吸附的树枝状聚合物对表面相互作用和摩擦的改性:2.高表面能-OH封端的碳硅烷树枝状聚合物

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The interactions between two mica surfaces bearing a fourth-generation carbosilane dendrimer (modified to expose -OH groups on its outer surface) were studied across a toluene medium, using a surface force balance capable of measuring shear as well as normal forces. Normal force measurements indicate that the dendrimers adsorb from dilute toluene solution (ca. 5 x 10(-4) w/w) as a monolayer on each surface. Two such interacting surfaces experience a longer-ranged van der Waals attraction followed by strong short-range adhesion (probably of dipolar origin) as the adsorbed dendrimers come into contact. Within the range of our parameters, the dendrimer layers were incompressible normal to the surfaces. Friction versus load profiles were measured at different shear velocities, revealing marked stick-slip sliding, whereas the magnitude of the yield stress increased with longer times of contact and with normal pressure. This suggests that over time scales comparable with the experimental times the interacting layers rearrange to optimize their interfacial shear strength. The behavior of these -OH-exposing carbosilane dendrimers differs qualitatively from that of CH3-exposing poly(propyleneimine) dendrimers studied earlier, a difference attributable to the much more polar nature of the hydroxyl groups. [References: 34]
机译:使用能够测量剪切力和法向力的表面力平衡,在甲苯介质上研究了带有第四代碳硅烷树枝状大分子(经修饰以暴露其外表面上的-OH基团)的两个云母表面之间的相互作用。法向力测量表明,树枝状聚合物从稀甲苯溶液(约5 x 10(-4)w / w)以单层形式吸附在每个表面上。当吸附的树枝状大分子接触时,两个这样的相互作用表面经历了范德华力更长距离的吸引,随后又发生了短距离的强烈粘附(可能是偶极起源)。在我们的参数范围内,树枝状聚合物层垂直于表面是不可压缩的。在不同的剪切速度下测量了摩擦与载荷的关系曲线,显示出明显的粘滑滑动,而屈服应力的大小随着接触时间的延长和法向压力的增加而增加。这表明在与实验时间相当的时间尺度上,相互作用层重新排列以优化其界面剪切强度。这些暴露于-OH的碳硅烷树枝状聚合物的行为与先前研究的暴露于CH3的聚(丙烯亚胺)树枝状聚合物的性质在质量上有所不同,这归因于羟基的极性更大。 [参考:34]

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