Electrophoretic mobility, velocity

As an optical detection system, electrophoretic light scattering has been frequently used in recent years [4], In this case, the collected signal of the particles movement shifted to higher or lower frequencies depending on their charge. The frequencies are then converted to electrophoretic mobilities, velocities, and finally zeta potentials. 

There are a number of complications in the experimental measurement of the electrophoretic mobility of colloidal particles and its interpretation see Section V-6F. TTie experiment itself may involve a moving boundary type of apparatus, direct microscopic observation of the velocity of a particle in an applied field (the zeta-meter), or measurement of the conductivity of a colloidal suspension. 

The velocity with which a solute moves through the conductive medium due to its electrophoretic mobility (Vep). 

In the presence of a buffer with constant composition across the electrophoretic chamber, the angle of deflection (0) of the solute in the electric field is dependent upon the intrinsic electrophoretic mobility of the solute (p. ), the linear velocity of the buffer (v) and the current through the chamber (I) and can be described as [17] ... 

The velocity of migration over the applied electric field is called the electrophoretic mobility (pe) ... 

The velocity of particle migration, v, across the field is a function of the surface charge or zeta potential and is observed visually by means of an ultramicroscope equipped with a calibrated eyepiece and a scale. The movement is measured by timing the individual particles over a certain distance, and the results of approximately 10-15 timing measurements are then averaged. From the measured particle velocity, the electrophoretic mobility (defined as v/E, where E is the potential gradient) can be calculated. 

If the electric field E is applied to a system of colloidal particles in a closed cuvette where no streaming of the liquid can occur, the particles will move with velocity v. This phenomenon is termed electrophoresis. The force acting on a spherical colloidal particle with radius r in the electric field E is 4jrerE02 (for simplicity, the potential in the diffuse electric layer is identified with the electrokinetic potential). The resistance of the medium is given by the Stokes equation (2.6.2) and equals 6jtr]r. At a steady state of motion these two forces are equal and, to a first approximation, the electrophoretic mobility v/E is... 

In order to influence a migration it is obvious that one can alter the charge of the compounds, the viscosity of the medium and the dynamic radius of the compounds. According to Eq. 17.5, the electrophoretic mobility is the proportionality factor in the linear relationship of the migration velocity and the electric field strength... 

The migration in CE is obviously influenced by both the effective and the electroosmotic mobility. Therefore, the proportionality factor in the relationship of the migration velocity and the electric field strength in such a case is called the apparent electrophoretic mobility (/iapp) and the migration velocity the apparent migration velocity (vapp). The /iapp is equal to the sum of /migration velocity is expressed as... 

The zeta potential can be measured by electrophoresis, which determines the velocity of particles in an electric field of known strength [144]. This particle velocity, v, can then be related to the electrical field strength, E, as the electrophoretic mobility, fi. This is shown by... 

Electrophoretic mobility measurements can be performed by laser Doppler anemometry (LDA). LDA is fast and capable of high resolution of particle velocities [144]. It measures particle velocity, which is measured in the stationary... 

Separations in CE are based on the different velocities of charged species when they encounter an electric field thus a key parameter in CE is electrophoretic mobility. Mobility (pi) is the rate of migration of sample components under a given set of conditions ... 

The separation mechanism is based on stereoselective ion-pair formation of oppositely charged cationic selector and anionic solutes, which leads to a difference of net migration velocities of the both enantiomers in the electric field. Thus, the basic cinchona alkaloid derivative is added as chiral counterion to the BGE. Under the chosen acidic conditions of the BGE, the positively charged counterion associates with the acidic chiral analytes usually with 1 1 stoichiometry to form electrically neutral ion-pairs, which do not show self-electrophoretic mobility but... 

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