Electrophoresis electro-osmosis

If a liquid moves tangential to a charged surface, then so-called electrokinetic phenomena arise [101]. Electrokinetic phenomena can be divided into four categories Electrophoresis, electro-osmosis, streaming potential, and sedimentation potential [102], In all these phenomena the zeta potential plays a crucial role. The classic theory of electrokinetic effects was proposed by Smoluchowski2 [103],... 

An indication of the surface potential can be obtained through electrokinetic measurements. Electrokinetic motion occurs when the mobile part of the electric double layer is sheared away from the inner layer (charged surface). Of the four types of electrokinetic measurements, electrophoresis, electro-osmosis, streaming potential, and sedimentation potential, the first finds the most use in industrial practise. In electrophoresis, an electric field is applied to a sample causing charged dispersed species, and any attached material or liquid, to move towards the... 

The above relationship shows that zeta potenticd is a little lower than the Stem potential and this is because it Is located further out from the surface of the macromolecule. The zeta potential of any colloidal solution can be calculated by electrokinetic measurements like electrophoresis, electro-osmosis and streaming potential. Though the methods are different, all lead to the same calculated value of the zeta potential for any particular system. All the methods involve the relative motion of the two surfaces in contact. 

Another effect which is important in a discussion of the conductivity of colloidal systems is the surface conduction, i.e. a conductivity contribution from the double-layers. This contribution is important when the electrolyte content is relatively low in the bulk phase. The surface conductance is also important when measurements of electrokinetic phenomena (electrophoresis, electro-osmosis, etc.) need to be evaluated. Recently, it... 

Charged polymers and colloids exhibit a wide variety of elec-trokinetic behavior with terms such as electrophoresis, electro-osmosis, streaming potential, sedimentation potential, and others. These have been thoroughly reviewed [50]. 

Electrokinetic phenomena, namely electrophoresis, electro-osmosis and streaming potential are discussed in Vol. 1 at a fundamental level. These effects arise because of charge separation at the interface that is induced for example by application of an electric field. The plane at which the liquid starts to move is defined as the shear plane and the potential at this plane is defined as the electrokinetic or zeta potential. A schematic picture is given that describes the shear plane and zeta potential. The latter is mostly assumed to be equal to the Stern potential and in the absence of specific adsorption it can be equated to the surface potential, which is the parameter... 

Stability of soi Electrophoresis Electro-osmosis Adsorption of capillary active molecules Abrasion dcctrode I " adsorption and counter ion concentration... 

Electro osmosis often accompanies electrophoresis. It is the transport of Hquid past a surface or through a porous soHd, which is electricaHy charged but immovable, toward the electrode with the same charge as that of the surface. Electrophoresis reverts to electroosmotic flow when the charged particles are made immovable if the electroosmotic flow is forcibly prevented, pressure builds up and is caHed electroosmotic pressure. 

Electrophoresis and electro osmosis can be used to enhance conventional cake filtration. Electrodes of suitable polarity are placed on either side of the filter medium so that the incoming particles move toward the upstream electrode, away from the medium. As most particles carry negative charge, the electrode upstream of the medium is usuaHy positive. The electric field can cause the suspended particles to form a more open cake or, in the extreme, to prevent cake formation altogether by keeping aH particles away from the medium. 

Electroosmotic flow in a capillary also makes it possible to analyze both cations and anions in the same sample. The only requirement is that the electroosmotic flow downstream is of a greater magnitude than electrophoresis of the oppositely charged ions upstream. Electro osmosis is the preferred method of generating flow in the capillary, because the variation in the flow profile occurs within a fraction of Kr from the wall (49). When electro osmosis is used for sample injection, differing amounts of analyte can be found between the sample in the capillary and the uninjected sample, because of different electrophoretic mobilities of analytes (50). Two other methods of generating flow are with gravity or with a pump. 

Factors Affecting Ionic Migration. Effect of Temperature. pH and Ionic Strength. Electro-osmosis. Supporting Medium. Detection of Separated Components. Applications of Traditional Zone Electrophoresis. High-performance Capillary Electrophoresis. Capillary Electrochromatography. Applications of Capillary El ectrochromatography. ... 

CEC has recently become an alternative to HPLC. A capillary is filled or its internal wall covered with a porous sorbent. The free volume remaining in the capillary is filled with an electrolyte. High voltage (on the order of ten kV) is applied across the length of the capillary. Sample plugs are introduced at one end. Sample components are carried to the other end due to electro-osmosis and - in the case of ions - also electrophoresis. In CEC the more important effect is electro-osmosis, which is essentially a flow mechanism of the electrolyte solution without the need for applied pressure. The separation of the sample components occurs mainly due to phase distribution between the stationary phase and the flowing electrolyte. Thus CEC is very similar to HPLC in a packed capillary except that the flow is not pressure driven and that ionic analytes undergo electrophoresis additionally to phase separation. 

Electro-osmosis - the movement of liquid relative to a stationary charged surface (e.g. a capillary or porous plug) by an applied electric field (i.e. the complement of electrophoresis). The pressure necessary to counterbalance electro-osmotic flow is termed the electro-osmotic pressure. 

Electrophoresis has the greatest practical applicability of these electrokinetic phenomena and has been studied extensively in its various forms, whereas electro-osmosis and streaming potential have been studied to a moderate extent and sedimentation potential rarely, owing to experimental difficulties. 

For well-dispersed colloid systems, particle electrophoresis has been the classic method of characterization with respect to electrostatic interactions. However, outside the colloidal realm, i.e., in the rest of the known world, the measurement of other electrokinetic phenomena must be used to characterize surfaces in this respect. The term electrokinetic refers to a number of effects induced by externally applied forces at a charged interface. These effects include electrophoresis, streaming potential, and electro-osmosis. 

One way to increase the range of measurement may be in the use of light scattering (Doppler electrophoresis) to determine particle velocities. Such methods are used in contemporary commercially available analytical particle electrophoresis apparatuses. However, presently available equipment is not designed for ready exchange (replacement) of chamber surfaces for electro-osmosis studies. 

Though the model presented and used does not give a complete account of the interface and the origin of measured electro-osmotic fluid mobility, it was proven useful in interpretation of surface properties. The range of electrolyte concentration that can be used in the manual particle electrophoresis chamber developed in this work is limited, and this limits the model of the origin of electro-osmosis that can be tested, such as inclusion of a Stern layer. 

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