Normal phase displacement model

The retention mechanism in the normal phase is often referred to as adsorption chromatography. It is described as the competition between analyte molecules and mobile-phase molecules on the surface of the stationary phase. It is assumed that the adsorbing analyte displaces an approximate equivalent amount of the adsorbed solvent molecules from the monolayer on the surface of the packing throughout the retention process [18]. The solvent molecules that cover the surface of the adsorbent may or may not interact with the adsorption sites, depending on the properties of the solvent. This retention model, proposed by Snyder, was originally used to describe retention with silica and alumnina adsorbents, but several other studies have shown that this model may also be used for polar bonded phases, such as diol, cyano, and amino bonded silica [10,19]. 

Polar-bonded stationary phases, such as cyanopropyl, diol, or aminopropyl, bonded to a silica matrix, have moderate polarity and can be used in normal- and reversed-phase (RP) systems. The retention behavior of heterocyclic bases was also examined using these adsorbents by determination of Rm (log k) values of solutes by the use of eluents with various modifier concentrations.It was statistically found that the Snyder-Soczewihski equation and Scott theory describe the retention of quinolines on polar-bonded stationary phases in normal-phase systems sufficiently well. It seems that results are consistent with a displacement model. The dispersive interactions between solute molecules and the polar component of an eluent seem also to have an important role. Similarly, the retention—... 

In its simplest form the competition model assumes the entire adsorbent surface is covered by a monolayer of solute and mobile phase molecules. Under normal chromatographic conditions, the concentration of sample molecules will be small and the adsorbed monolayer will consist mainly of mobile phase molecules. Retention of a solute molecule occurs by displacing a roughly equivalent volume of mobile phase molecules from the monolayer to make the surface accessible to the adsorbed solute aiolecule. For elution of the solute to occur -the above process must be reversible, and can be represented by the equilibrium depicted by equation (4.6)... 

Latora et al. [18] discussed a relation between the process of relaxation to equilibrium and anomalous diffusion in the HMF model by comparing the time series of the temperature and of the mean-squared displacement of the phases of the rotators. They showed that anomalous diffusion changes to a normal diffusion after a crossover time, and they also showed that the crossover time coincides with the time when the canonical temperature is reached. They also claim that anomalous diffusion occurs in the quasi-stationary states. 

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