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Journal ArticleDOI

The Effect of Electrostatic Forces on Electrokinetic Potentials

W. G. Eversole, +1 more
- 01 Nov 1941 - 
- Vol. 9, Iss: 11, pp 798-801
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TLDR
In this paper, it is shown that the potential gradient normal to the wall is determined principally by the valence and concentration of the ion of opposite charge to a charged wall, and the surface potential of the wall and the thickness of the immobilized liquid layer are calculated from electrokinetic potential data.
Abstract
Assuming that the ions in solution near a charged wall are subjected only to electrostatic and kinetic forces, it is shown that the potential gradient normal to the wall is determined principally by the valence and concentration of the ion of opposite charge to the wall. Assuming that the valence and concentration of this ion determine the effect of the salt on the electrokinetic potential of the wall, the surface potential of the wall and the thickness of the immobilized liquid layer are calculated from electrokinetic potential data. Salts of ``normal'' ions (NaCl, BaCl2, etc.) cause relatively small changes in the surface potential and thickness of the immobilized layer at a glass surface and these changes occur only at very low salt concentrations. Salts containing ``abnormal'' ions (H+, OH—, La+++, etc.) produce larger changes and the change continues over a much wider concentration range. The extreme effectiveness of salts like AlCl3 and ThCl4 in lowering negative electrokinetic potentials cannot be accounted for by the higher valence of the ions.

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Citations
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Journal ArticleDOI

The work function of emersed electrodes

TL;DR: In this article, the work function of the electrodes is shown to be independent of the electrode material, and linearly dependent with unity slope upon the electrode potential applied before and during emersion.
Journal ArticleDOI

Surface activity and emulsification properties of hydrophobically modified dextrans.

TL;DR: Neutral polymeric surfactants synthesized by covalent attachment of hydrophobic groups onto a polysaccharide backbone (dextran) behaved like classical associative polymers as demonstrated by viscometric measurements.
Journal ArticleDOI

Surface modification of poly(lactic acid) nanospheres using hydrophobically modified dextrans as stabilizers in an o/w emulsion/evaporation technique

TL;DR: Photon correlation spectroscopy, zetametry, and differential scanning calorimetry studies corroborated that interfacial adhesion between immiscible dextran and PLA chains was achieved by compatibilization of polymer segments via hydrophobic groups grafted onto deXTran and thus leading to the formation of entanglements between the hydrophobically modified dextrans parts and the PLA matrix.
Journal ArticleDOI

Influence of polymeric surfactants on the properties of drug-loaded PLA nanospheres

TL;DR: Different dextran derivatives containing various grafted hydrophobic groups were synthesized and their applicability as emulsion stabilizers in the preparation of poly(lactic acid) (PLA) nanospheres by an o/w emulsion/evaporation technique was investigated as mentioned in this paper.
Journal ArticleDOI

Adsorption of plasma proteins onto polymer latices.

TL;DR: The protein adsorption was studied as a function of pH, ionic strength and electrolyte concentration and the adsorbability of heat- and urea-denatured albumins was investigated, finding a higher affinity of denatured components for polymer latices was observed compared with that of the native components.
References
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Journal ArticleDOI

Evidence for a Rigid Multilayer at a Solid‐Liquid Interface

TL;DR: The assumption of immobile hydrous multilayer at a wall of fixed potential was used in deriving equations relating zeta potentials, concentrations of univalent salt solution, wall potential, and thickness of the immobile layer as mentioned in this paper.
Journal ArticleDOI

Strömungspotentiale und Kolloidstabilität, II

TL;DR: In this paper, an Kapillaren von Jenaglas 59 III und von Quarz wurde eine gleiche starke Aufladung with Lauge gefunden.
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