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High performance chromatographic separations

Compared to hydrocarbonaceous silica RPC sorbents, not as much commitment has been made to the development of bonded, polar-phase sorbents suitable for the high-performance chromatographic separation of peptides. Due to polar, notably hydrogen bonding, interactions between the peptide and the hydrophilic surface of the sorbent useful selectivity effects can, however, be achieved. In fact, at least two types of separation mechanisms can be identified with bonded polar-phase sorbents. In the first mode, the peptides do not interact per se with the bonded polar-phase sorbent but, rather, are separated on the basis of their ability to permeate into the pores and elute in order of their hydrodynamic volume. In this mode, peptides are separated by steric exclusion effects, with the retention (in terms of elution volume, Ve) of a partial retained peptide, Pb described by the following relationships ... [Pg.603]

Mao, C. and Tucker, S. A., High-performance chromatographic separation of polycyclic aromatic hydrocarbons using pyridinium chloride as a selective fluorescence quencher to aid detection, J. Chromatogr. A, 966, 53-61, 2002. [Pg.613]

Fig. 6c. The sample is electrokinetically transported into the analysis channel. To terminate sample flow into the analysis channel, the electric potential at the buffer reservoir is reapplied (Fig. 6d). A small quantity of sample is dispensed into the analysis channel as shown in Fig. 6d. Due to the directionality of the buffer flow, i. e., traveling from left to right as pictured, the rear of the sample plug is triangular in shape but disappears in about one second due to the transverse diffusion within the analysis channel. The asymmetric shape observed at the rear of the sample plug does not hinder high-performance chromatographic separations which employ the gated valve. Fig. 6c. The sample is electrokinetically transported into the analysis channel. To terminate sample flow into the analysis channel, the electric potential at the buffer reservoir is reapplied (Fig. 6d). A small quantity of sample is dispensed into the analysis channel as shown in Fig. 6d. Due to the directionality of the buffer flow, i. e., traveling from left to right as pictured, the rear of the sample plug is triangular in shape but disappears in about one second due to the transverse diffusion within the analysis channel. The asymmetric shape observed at the rear of the sample plug does not hinder high-performance chromatographic separations which employ the gated valve.
Feibush, B. and Santasania, C. T., Hydrophilic shielding of hydrophobic, cation- and anion-exchange phases for separation of small analytes direct injection of biological fluids onto high performance chromatographic columns, /. Chromatogr., 544, 41, 1991. [Pg.277]

Knox, J.H. and Laird, G.R. Soap chromatography a new high performance chromatographic technique for separation of ionizahle materials dyestuff intermediates. J. Chromatogr. 1976, 122, 17-34. [Pg.51]

Despite the values of AAG s being generally small, they are large enough to be resolved by high performance chromatographic methods such as gas and liquid chromatography. Thousands of successful separations of enantiomers by CD... [Pg.16]

Thermodynamic equilibration is an important factor for achieving highly efficient chromatographic separations, whereas FI separations are almost always performed under non-equilibrated conditions in order to achieve optimum performance. Thus, in FI separation procedures, completeness of the separation reaction, and therefore of analyte recovery are not pursued. This will not deteriorate the precision or accuracy of the results as long as the losses are reproducible and the systems are properly calibrated. [Pg.20]

Trace a (Fig. 2-4) was obtained with a virtually straight column, having a relatively wide inner diameter (0.54 mm). Trace b shows that the same columns but tightly colled into a helical shape, performs much better. Thus the favorable coiling effects in high-speed chromatographic separation... [Pg.32]

Chromatographic Method. Progress in the development of chromatographic techniques (55), especially, in high performance Hquid chromatography, or hplc, is remarkable (56). Today, chiral separations are mainly carried out by three hplc methods chiral hplc columns, achiral hplc columns together with chiral mobile phases, and derivatization with optical reagents and separation on achiral columns. All three methods are usehil but none provides universal appHcation. [Pg.279]


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Chromatographic performance

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