Plates
The term plates in chromatography refer to ’theoretical plates’. In the development of an equation for the elution curve of a solute in chromatography equilibrium must be assumed but in a chromatographic system equilibrium is never actually obtained. As a consequence, a mathematical concept must be introduced deal with this problem. This non-equilibrium condition arises from the dynamic nature of the distribution systems as the mobile phase is continually flowing past the stationary phase. The solute does not spend sufficient time at any point in the column for equilibrium to be achieved. To avoid this difficulty in the theoretical treatment of retention, the column is considered to be divided into a number of theoretical plates or cells and each is allotted a finite height (or length) that will allow the solute sufficient theoretical ‘dwell-time’ for equilibrium to take place. It is clear that the faster the equilibrium, the smaller the theoretical plate, and the more theoretical plates there will be in the column. Thus, the more efficient column has more theoretical plates. The use of the theoretical plate is discussed in detail in the plate theory
Author: RPW Scott
Book:Plate Theory and Extensions
Section:Plate-Theory Column-Efficiency
Column Efficiency
The column
efficiency is defined as the number of theoretical plates in the column. As
discussed in the plate theory, the faster the equilibrium process, the smaller
the plates and thus, the greater the number of plates in the column. It is
therefore important to know how to determine the number of plates a column
possesses and the relationship of the number of theoretical plates in the
column to the properties of the chromatogram.
Starting with
the Poisson form of the elution equation, the peak width at the points of
inflexion (which corresponds to
Plate-Theory Column-Efficiency
Author: RPW Scott
Book:Plate Theory and Extensions
Section:Plate-Theory Derivation
nbsp;
dXs = KdXm (2)
Consider three
consecutive plates in a column, the (p-1), the (p) and the (p+1) plates and let
there be a total of (n) plates in the column. The three plates are depicted in
Figure 2.
Figure 2. Three Consecutive
Theoretical Plates in a Column
Let the
volumes of mobile phase and stationary phase in each plate be (vm)
and (vs) respectively, and the concentrations of solute in the
mobile and stationary phase in each plate be Xm(p-1), Xs(p-1),
Xm(p), Xs(p), Xm(p+1), and Xs(p+1), respectively.
Let a
Plate-Theory Derivation
Author: RPW Scott
Book:Extra Column Dispersion
Section:EC-Dispersion Small-Bore-Columns
The column was
10 m long, 1 mm I.D. packed with Partisil Silica Gel 20 mm particle diameter. At the optimum flow rate (i.e., 10 ml/min.) the column gave a quarter of a
million theoretical plates. However, the chromatogram shown in figure 34 was
obtained at a flow rate of 38 ml/min.
and, thus, as it was operated well above its optimum velocity, the column only
gave an efficiency of 160,000 theoretical plates. As the chromatographic data
was acquired and processed by a computer portions of the chromatogram could be
expanded and these are shown as inserts in the figure. It is seen that the
apparently confused peaks at the start of the chromatogram are, in fact, well
resolved into
EC-Dispersion Small-Bore-Columns
Author: RPW Scott
Book:Plate Theory and Extensions
Section:Plate-Theory Effective-Plate-Number
;
Consequently,
(57)
Equation (57)
shows the relationship between efficiency and 'effective plates'. The number of
'effective plates' in a column is not an arbitrary measure, but is directly related to efficiency as derived from
the plate theory. Equation (57)shows that, as (k') becomes large, (n) and (NE) converge to the same value
Plate-Theory Effective-Plate-Number
Author: RPW Scott
Book:Liquid Chromatography Detectors
Section:HPLC-Detectors Refractive-Index-Based Dielectric-Constant
will hold:
The
resistance-component of the cell reduces the bridge sensitivity to changes in
capacity and thus the plates should be well insulated to prevent conductivity
through the mobile phase.
The capacity
of the sensor can also be measured by making it one component of a
resistance/capacity or an inductance/capacity oscillator. The frequency will
depend, among other things, on the capacity of the sensor and, in turn, on the
dielectric constant of the material between the plates. The frequency general
can be heterodyned against a reference oscillator and the frequency difference
will then be proportional to the change in capacity and hence the dielectric
constant of the mobile phase.
Poppe and
Kunysten (28) described a dielectric constant detector which included a
reference cell for temperature compensation. The cell consisted of two
stainless steel plates 2 cm x 1 cm x
1 mm separated by a gasket 50 mm
thick. The two cells were identical and clamped
HPLC-Detectors Refractive-Index-Based Dielectric-Constant
Author: RPW Scott
Book:Dispersion in Chromatography Columns
Section:Dispersion Van-Deemter-Equation
nbsp;
Figure 12.
Graph of Log. Maximum Efficiency against Particle Diameter
It is seen from
figure 12 that changing the particle diameter from 1 to 20 micron results in an
efficiency change from about 3500 theoretical plates to nearly 1.5 million theoretical plates and furthermore,
this very high efficiency is achieved at an inlet
pressure of only 3000 p.s.i.. It is also seen that the maximum available
efficiency increases as the particle diameter increases. This is because, as
already discussed, if the pressure is limited, in order to increase the column
length to provide more theoretical plates, the permeability of the column must
be increased to allow the optimum mobile phase velocity to be realized. It is
Dispersion Van-Deemter-Equation