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Forces between charged surfaces

Ruckenstein and Schiby derived4 an expression for the electrochemical potential, which accounted for the hydration of ions and their finite volume. The modified Poisson-Boltzmann equation thus obtained was used to calculate the force between charged surfaces immersed in an electrolyte. It was shown that at low separation distances and high surface charges, the modified equation predicts an additional repulsion in excess to the traditional double layer theory of Deijaguin—Landau—Verwey—Overbeek. [Pg.331]

Apparently, mechanisms of low-salinity waterflooding are related to the DLVO theory, which is named after Derjaguin, Landau, Verwey, and Overbeek. The theory describes the force between charged surfaces interacting through a liquid medium. It combines the effects of the van der Waals attraction and the electrostatic repulsion due to the so-called double layer of counter ions. [Pg.72]

Kocevar K, Musevic I (2002) Observation of an electrostatic force between charged surfaces in hquid crystals. Phys Rev E 65 030703... [Pg.47]

One fascinating feature of the physical chemistry of surfaces is the direct influence of intermolecular forces on interfacial phenomena. The calculation of surface tension in section III-2B, for example, is based on the Lennard-Jones potential function illustrated in Fig. III-6. The wide use of this model potential is based in physical analysis of intermolecular forces that we summarize in this chapter. In this chapter, we briefly discuss the fundamental electromagnetic forces. The electrostatic forces between charged species are covered in Chapter V. [Pg.225]

The most frequent type of interaction between solid and species in solution would be electrostatic adsorption (ion exchange), due to the action of attractive coulomb forces between charged particles in solution and the solid surfaces. This process would also be concentration dependent. [Pg.286]

Coulombic explosion The process by which a droplet disintegrates into a number of smaller droplets which occurs when the repulsive forces between charges on the surface of a droplet are greater than the cohesive force of surface tension. [Pg.304]

Surface forces measurement is a unique tool for surface characterization. It can directly monitor the distance (D) dependence of surface properties, which is difficult to obtain by other techniques. One of the simplest examples is the case of the electric double-layer force. The repulsion observed between charged surfaces describes the counterion distribution in the vicinity of surfaces and is known as the electric double-layer force (repulsion). In a similar manner, we should be able to study various, more complex surface phenomena and obtain new insight into them. Indeed, based on observation by surface forces measurement and Fourier transform infrared (FTIR) spectroscopy, we have found the formation of a novel molecular architecture, an alcohol macrocluster, at the solid-liquid interface. [Pg.3]

The force between charged objects and surfaces in an electrolyte solution is mediated by the ions and the solvent. This is referred to as solvation forces or electrolyte-mediated... [Pg.637]

Figure 2.14 Measured electrostatic double-layer and van der Waals forces between two surfaces of curved mica of radius 1 cm in (a) water and (b) dilute KNO3 and Ca(N03)2 solutions. The lines are the predictions of the DLVO theory with a Hamaker constant of 2.2 x 10 J in the limits of constant surface charge and constant surface potential here xfrQ = -(j/s, the particle surface potential. (The lines for constant surface charge are slightly higher than those for constant surface potential at small D.) The inset in (b) is the measured force in 0.1 M KNO3, which shows a force minimum at a distance of around 7 nm. Since this minimum in force occurs away from the deep minimum at the surface, it is called a secondary minimum. (From Israelachvili and Adams 1978 and Israelachvili 1992, reprinted with permission from Academic Press.)... Figure 2.14 Measured electrostatic double-layer and van der Waals forces between two surfaces of curved mica of radius 1 cm in (a) water and (b) dilute KNO3 and Ca(N03)2 solutions. The lines are the predictions of the DLVO theory with a Hamaker constant of 2.2 x 10 J in the limits of constant surface charge and constant surface potential here xfrQ = -(j/s, the particle surface potential. (The lines for constant surface charge are slightly higher than those for constant surface potential at small D.) The inset in (b) is the measured force in 0.1 M KNO3, which shows a force minimum at a distance of around 7 nm. Since this minimum in force occurs away from the deep minimum at the surface, it is called a secondary minimum. (From Israelachvili and Adams 1978 and Israelachvili 1992, reprinted with permission from Academic Press.)...

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