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Interaction of Monovalent Ions with Hydrophobic and Hydrophilic Colloids: Charge Inversion and Ionic Specificity

机译:一价离子与疏水和亲水胶体的相互作用:电荷反转和离子特异性

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摘要

Here we study experimentally and by simulations the interaction of monovalent organic and inorganic anions with hydrophobic and hydrophilic colloids. In the case of hydrophobic colloids, our experiments show that charge inversion is induced by chaotropic inorganic monovalent ions but it is not induced by kosmotropic inorganic anions. For organic anions, giant charge inversion is observed at very low electrolyte concentrations. In addition, charge inversion disappears for both organic and inorganic ions when turning to hydrophilic colloids. These results provide an experimental evidence for the hydrophobic effect as the driving force for both ion specific effects and charge inversion. In the case of organic anions, our molecular dynamics (MD) simulations with full atomic detail show explicitly how the large adsorption free energies found for hydrophobic colloids are transformed into large repulsive barriers for hydrophilic colloids. Simulations confirm that solvation free energy (and hence the hydrophobic effect) is responsible for the build up of a Stern layer of adsorbed ions and charge inversion in hydrophobic colloids and it is also the mechanism preventing charge inversion in hydrophilic colloids. Overall, our experimental and simulation results suggest that the interaction of monovalent ions with interfaces is dominated by solvation thermodynamics, that is, the chaotropic/kosmotropic character of ions and the hydrophobic/hydrophilic character of surfaces.
机译:在这里,我们通过实验和模拟研究一价有机和无机阴离子与疏水和亲水胶体的相互作用。对于疏水性胶体,我们的实验表明,电荷离解是由离液型无机一价离子诱导的,而不是由共溶性无机阴离子诱导的。对于有机阴离子,在非常低的电解质浓度下会观察到巨大的电荷反转。此外,转向亲水性胶体时,有机和无机离子的电荷反转都消失了。这些结果为疏水效应作为离子特异性效应和电荷反转的驱动力提供了实验证据。在有机阴离子的情况下,我们的分子动力学(MD)模拟具有完整的原子详细信息,明确显示了疏水性胶体的大量吸附自由能如何转化为亲水性胶体的大排斥性屏障。模拟证实,溶剂化自由能(以及由此产生的疏水效应)是疏水离子胶体中斯特恩层的堆积和电荷反转的原因,也是防止亲水胶体中电荷反转的机制。总的来说,我们的实验和模拟结果表明,一价离子与界面的相互作用主要受溶剂化热力学的影响,即离子的离液/共溶特性和表面的疏水/亲水特性。

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  • 来源
    《Journal of the American Chemical Society》 |2011年第38期|p.15025-15035|共11页
  • 作者单位

    Institut de Ciencia de Materials de Barcelona (ICMAB-CSIC), Campus de la UAB, 08193 Bellaterra, Spain;

    Institut de Ciencia de Materials de Barcelona (ICMAB-CSIC), Campus de la UAB, 08193 Bellaterra, Spain;

    Biocolloid and Fluid Physics Group, Department of Applied Physics, University of Granada, Avenida Fuentenueva S/N, 18071 Granada, Spain;

  • 收录信息 美国《科学引文索引》(SCI);美国《工程索引》(EI);美国《生物学医学文摘》(MEDLINE);美国《化学文摘》(CA);
  • 原文格式 PDF
  • 正文语种 eng
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  • 入库时间 2022-08-18 03:14:27

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