Plate models, chromatography

Golay equation 21, 611 gradient (LC) 490 height equivalent to a theoretical plate 11 longitudinal diffusion 16 mass transfer resistance 17 nonlinear chromatography SOS plate model 14 rate theory IS reduced parameters 78, 361, 611... 

The theoretical parameters of isocratic chromatography are often described using the plate model. One can imagine the analyte to be distributed... 

Plate model A model of chromatography which assumes that the column is a series of stages in each of which equUibrimn between the stationary and the mobile phase is achieved. 

For half a century different theories have been and continue to be proposed to model chromatography and to explain the migration and separation of analytes in the column. The best known are those employing a statistical approach (stochastic theory), the theoretical plate model or a molecular dynamics approach. 

Figure 21.4 Application of the theoretical plate model of chromatography to evaluate on-column reactions in a chromatographic setup. Each theoretical plate is considered as chemical reactor.

Chromatography is based on the same principle as adsorption. Chromatographic techniques can be used to measure a wide variety of thermodynamic, kinetic, and physico-chemical properties. Separation occurs because of differing velocities of travel of components in the mobile and stationary phases. Theoretical plate model can be applied to chromatography. Chromatographic methods can be classified as gas and liquid chromatography depending on the nature of the mobile phase. 

In their original theoretical model of chromatography, Martin and Synge treated the chromatographic column as though it consists of discrete sections at which partitioning of the solute between the stationary and mobile phases occurs. They called each section a theoretical plate and defined column efficiency in terms of the number of theoretical plates, N, or the height of a theoretical plate, H where... 

The theoretical work that exploited the advantages of the multidimensional separation format appears to have been developed much later than the original experimental work. One of the earliest studies was conducted by Connors (1974), who assumed that the distribution of spots on a two-dimensional thin-layer chromatography (2DTLC) plate could be modeled using a Poisson distribution of data on each retention axis. He then constructed equations that related the number of chromatographic systems needed to resolve a specific number of compounds. One... 

Fig. 3. Diagrams of electrochemical cells used in flow systems for thin film deposition by EC-ALE. A) First small thin layer flow cell (modeled after electrochemical liquid chromatography detectors). A gasket defined the area where the deposition was performed, and solutions were pumped in and out though the top plate. Reproduced by permission from ref. [ 110]. B) H-cell design where the samples were suspended in the solutions, and solutions were filled and drained from below. Reproduced by permission from ref. [111]. C) Larger thin layer flow cell. This is very similar to that shown in 3A, except that the deposition area is larger and laminar flow is easier to develop because of the solution inlet and outlet designs. In addition, the opposite wall of the cell is a piece of ITO, used as the auxiliary electrode. It is transparent so the deposit can be monitored visually, and it provides an excellent current distribution. The reference electrode is incorporated right in the cell, as well. Adapted from ref. [113],...

CH ROM PLATE - Stagewise Linear Model for Chromatography Columns System... 

A number of kinetic models of various degree of complexity have been used in chromatography. In linear chromatography, all these models have an analytical solution in the Laplace domain. The Laplace-domain solution makes rather simple the calculation of the moments of chromatographic peaks thus, the retention time, the peak width, its number of theoretical plates, the peak asymmetry, and other chromatographic parameters of interest can be calculated using algebraic expressions. The direct, analytical inverse Laplace transform of the solution of these models usually can only be calculated after substantial simplifications. Numerically, however, the peak profile can simply be calculated from the analytical solution in the Laplace domain. 

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