分子クラスターの水分和殻厚さの直接決定
Xiaohan Xu1, Ruixin Li1, Kexing Xiao1
1School of Polymer Science and Polymer Engineering, The University of Akron, Akron, Ohio 44325, United States.
Abstract:
A general approach is developed by using the analytical ultracentrifugation (AUC) technique through sedimentation velocity (SV) experiments to measure the hydration shell thicknesses of a series of macro-ionic, structurally well-defined metal oxide and metal peroxide molecular clusters in aqueous solution. These clusters with known molar masses and bare sizes serve as valuable models where the accurate hydration shell thickness can be determined by comparing the bare cluster size and its hydrodynamic size from AUC studies. The molecular clusters investigated here have sizes ranging from ∼1 nm to 3 nm. Within the experimental range, the hydration shell thickness increases from less than 0.1 nm for Keggin clusters to ∼0.6 nm for heavily charged clusters (up to 0.79 C/m2). For those relatively large clusters, the relationship between their hydration shell thickness and surface charge density can be described by a linear equation. However, hydration shells of Keggin clusters are found to be negligible. Weak acid-type clusters with pH-dependent charge density (here {Mo72Fe30}) show thicker hydration shells with heavier charge density (at higher pH). Meanwhile, temperature appears to have a minimal effect on the hydration shell within the experimental range, as higher temperatures result in only slightly thinner hydration shells.
関連する概念動画
Aqueous Solutions and Heats of Hydration
When ionic compounds dissolve in water, the ions in the solid separate and disperse uniformly throughout the solution because water molecules surround and solvate the ions, reducing the strong electrostatic forces between them. This process...
Molecular Geometry and Dipole Moments
Molecular Orbital Theory II
Molecular Shapes
Two regions of electron density in a diatomic...
Intermolecular Forces
Regioselectivity and Stereochemistry of Acid-Catalyzed Hydration


