This book treats the different current as well as unusual and hitherto often unstudied physico-chemical and surface-thermodynamic properties of water that govern all polar interactions occurring in it. These properties include the hyper-hydrophobicity of the water-air interface, the cluster formation of water molecules in the liquid state and the concomitant variability of the ratio of the electron-accepticity to electron-donicity of liquid water as a function of temperature, T. The increase of that ratio with T is the cause of the increase in hydration repulsion (“hydration pressure”) between polar surfaces upon heating, when they are immersed in water. The book also treats the surface properties of apolar and polar molecules, polymers, particles and cells, as well as their mutual interaction energies, when immersed in water, under the influence of the three prevailing non-covalent forces, i.e., Lewis acid-base (AB), Lifshitz-van der Waals (LW) and electrical double layer (EL) interactions. The polar AB interactions, be they attractive or repulsive, typically represent up to 90% of the total interaction energies occurring in water. Thus the addition of AB energies to the LW + EL energies of the classical DLVO theory of energy vs. distance analysis makes this powerful tool (the Extended DLVO theory) applicable to the quantitative study of the stability of particle suspensions in water. The influence of AB forces on the interfacial tension between water and other condensed-phase materials is stressed and serves, inter alia, to explain, measure and calculate the driving force of the hydrophobic attraction between such materials (the “hydrophobic effect”), when immersed in water. These phenomena, which are typical for liquid water, influence all polar interactions that take place in it. All of these are treated from the viewpoint of the properties of liquid water itself, including the properties of advancing freezing fronts and the surface prope

Key Features

- Explains and allows the quantitative measurement of hydrophobic attraction and hydrophilic repulsion in water - Measures the degree of cluster formation of water molecules - Discusses the influence of temperature on the cluster size of water molecules - Treats the multitudinous effects of the hyper-hydrophobicity of the water-air interface


Colloid scientists; chemical and biomedical engineers; physical chemists; biochemists; biophysicists; biologists; pharmacologistas; phartmaceutical scientists; microbiologists and graduate students in these disciplines

Table of Contents

1. General and Historical Introduction SECTION A. NON-COVALENT ENERGIES OF INTERACTION – EQUATIONS AND COMBINING RULES 2. The Apolar and Polar Properties of Liquid Water and other Condensed-phase Materials 3. The Extended DLVO Theory SECTION B: SURFACE THERMODYNAMIC PROPERTIES OF WATER WITH RESPECT TO CONDENSED-PHASE MATERIALS IMMERSED IN IT 4. Determination of Interfacial Tensions Between Water and other Condensed-phase Materials 5. The Interfacial Tension/Free Energy of Interaction Between Water and Identical Condensed-phase Entities, I, Immersed in Water, w 6. The Interfacial Tension/Free Energy of Interaction between Water and Two Different Condensed-phase Entities, I, Immersed in Water, w 7. Aqueous Solubility and Insolubility 8. Stability Versus Flocculation of Aqueous Particle Suspensions SECTION C: PHYSICAL AND PHYSICOCHEMICAL PROPERTIES OF WATER 9. Cluster Formation in Liquid Water 10. Hydration Energies of Atoms and Small Molecules in Relation to Clathrate Formation 11. The Water-air Interface 12. Influence of the pH and the Ionic Strength of Water on Contact Angles Measured with Drops of Aqueous Solutions on Electrically Charged, Amphoteric and Uncharged Surfaces 13. Macroscopic and Microscopic Aspects of Repulsion Versus Attraction in Adsorption and Adhesion in Water 14. Specific Interactions in Water Bibliography


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© 2008
Academic Press
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