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Density depletion at solid-liquid interfaces: A neutron reflectivity study

机译:固液界面的密度损耗:中子反射率研究

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Neutron reflectivity experiments conducted on self-assembled monolayers (SAMs) against polar (water) and nonpolar (organic) liquid phases reveal further evidence for a density reduction at hydrophobic-hydrophilic interfaces. The density depletion is found at the interface between hydrophobic dodecanethiol (C12) and hexadecanethiol (C16) SAMs and water and also between hydrophilic SAMs (C12/C11OH) and nonpolar fluids. The results show that the density deficit of a fluid in the boundary layer is not unique to aqueous solid-liquid interfaces but is more general and correlated with the affinity of the liquid to the solid surface. In water the variation of pH has only minor influence, while different electrolytes taken from the Hofmeister series seem to increase the depletion. On hydrophobic SAMs an increase in density depletion with temperature was observed, in agreement with Monte Carlo simulations performed on corresponding model systems. The increase in the water density depletion layer is governed by two effects: the surface energy difference between water and the substrate and the chemical potential of the aqueous phase.
机译:针对极性(水)和非极性(有机)液相的自组装单分子膜(SAM)进行的中子反射率实验揭示了疏水-亲水界面密度降低的进一步证据。在疏水性十二烷硫醇(C12)和十六烷硫醇(C16)SAM与水之间的界面以及亲水性SAM(C12 / C11OH)与非极性流体之间的界面处发现了密度消耗。结果表明,边界层中流体的密度不足并不是固液界面的唯一现象,而是更为普遍的,并且与液体对固体表面的亲和力有关。在水中,pH的变化影响很小,而从Hofmeister系列中提取的不同电解质似乎会增加消耗。在疏水性SAM上,观察到密度损耗随温度增加,这与在相应模型系统上执行的Monte Carlo模拟一致。水密度耗尽层的增加受两个作用支配:水与底物之间的表面能差和水相的化学势。

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