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Stationary phase efficiency parameter

As mentioned earlier, CEC couples the separating power of HPLC and the high efficiency of CE. The packed capillary can be considered the heart of the CEC system because it acts as a pump and provides chromatographic selectivity. The design of the stationary phase related parameters such as mobile phase and pH and instrumental parameters such as pressurization, injection modes, temperature, and voltage polarity play an important role in this technique. [Pg.256]

Typical normal-phase operations involved combinations of alcohols and hexane or heptane. In many cases, the addition of small amounts (< 0.1 %) of acid and/or base is necessary to improve peak efficiency and selectivity. Usually, the concentration of polar solvents such as alcohol determines the retention and selectivity (Fig. 2-18). Since flow rate has no impact on selectivity (see Fig. 2-11), the most productive flow rate was determined to be 2 mL miiT. Ethanol normally gives the best efficiency and resolution with reasonable back-pressures. It has been reported that halogenated solvents have also been used successfully on these stationary phases as well as acetonitrile, dioxane and methyl tert-butyl ether, or combinations of the these. The optimization parameters under three different mobile phase modes on glycopeptide CSPs are summarized in Table 2-7. [Pg.52]

Packed column SFC and CE are both able to make inroads into the application area served by HPLC, but from opposite extremes of polarity and with little overlap. CE is likely to be more efficient and faster, but mostly applicable to very polar molecules and ions. SFC qualifies as a more reproducible, trace technique, with greater selectivity and multiple detection options. HPLC and CE have been compared [365], Owing to their orthogonality, CZE and SFC are worth developing, not in competition or as an alternative to HPLC, but as an additional method in order to augment the information obtained from the analysis. With the broad scope of possible eluents and stationary phases, HPLC has fewer constraints than SFC and CZE. The parameters influencing selectivity may be used as a guide to optimisation (Table 4.44). [Pg.245]

In preparative chromatography, selectivity and efficiency no longer have the same importance they do in analytical chromatography. A certain selectivity is required in preparative chromatography as everywhere else in order to achieve the separation, but other parameters are at least as important if not more so. These include the loading capacity of the stationary phase and the maximum speed (throughput) of the process. The three main economic criteria for a large scale separation process are... [Pg.212]

In the development and optimization of a comprehensive LCxLC method, many parameters have to be taken in acconnt in order to accomplish snccessfnl separations. First of all, selectivity of the columns used in the two dimensions must be different to get maximum gain in peak capacity of the 2D system. For the experimental setup, column dimensions and stationary phases, particle sizes, mobile-phase compositions, flow rates, and second-dimension injection volumes should be carefully selected. The main challenges are related to the efficient coupling of columns and the preservation of mobile phase/column compatibility. [Pg.111]

Chromatographic Resolution. To optimize column-coating conditions and operating parameters glass capillary columns coated with various silicone-based stationary phases were tested with difficult-to-separate groups of PAH standards and Complex samples. The SE5 -coated columns performed excellently with respect to separation efficiency, column bleed and long-term stability. Other observers have had similar results with this... [Pg.358]

Hence, resolution, a key criterion for HPLC column users, is maximized for a given mobile phase/stationary phase system by maximizing N. Therefore, even if researchers are inclined to measure h as their column efficiency parameter, manufacturers... [Pg.32]

As we discussed above, efficiency and selectivity are complementary descriptors dependent on the different sets of chromatographic parameters. Efficiency is more dependent on the quality of the column packing, particle size, flow rate, and instrumental optimization, while selectivity is more dependent on the stationary phase properties and the nature of the analytes themselves. However, efficiency is sometimes affected by nonideal interactions of the analyte with the stationary phase (i.e., peak tailing). [Pg.22]

For a given type of stationary phase, the efficiency of a column is mainly determined by the column length and the packing procedure. The quality of a packing technique can easily be derived from well-defined parameters (i) the... [Pg.954]

Retention of Rohrschneider-McReynolds standards of selected chiral alcohols and ketones was measured to determine the thermodynamic selectivity parameters of stationary phases containing (- -)-61 (M = Pr, Eu, Dy, Er, Yb, n = 3, R = Mef) dissolved in poly(dimethylsiloxane) . Separation of selected racemic alcohols and ketones was achieved and the determined values of thermodynamic enantioselectivity were correlated with the molecular structure of the solutes studied. The decrease of the ionic radius of lanthanides induces greater increase of complexation efficiency for the alcohols than for the ketone coordination complexes. The selectivity of the studied stationary phases follows a common trend which is rationalized in terms of opposing electronic and steric effects of the Lewis acid-base interactions between the selected alcohols, ketones and lanthanide chelates. The retention of over fifty solutes on five stationary phases containing 61 (M = Pr, Eu, Dy, Er, Yb, n = 3, R = Mef) dissolved in polydimethylsiloxane were later measured ". The initial motivation for this work was to explore the utility of a solvation parameter model proposed and developed by Abraham and coworkers for complexing stationary phases containing metal coordination centers. Linear solvation... [Pg.721]

Selectivity is a function of the efficiency of the stationary phase with respect to its interactions with the solute vapor. Selection of an appropriate liquid stationary phase will even allow the separation of compounds that have the same vapor pressure. Separation is thus determined by the solubilities of the respective solutes in the stationary phase. Hence, the partition coefficient, k, is an extremely important parameter and is given by the following relationship ... [Pg.466]

I = 21 y = 0.394 r = 0.9476 F = 49.8 where log P is the hydrophobicity, bondrefr is the molecular refractivity, delta is the submolecular polarity parameter, ind indicator variable (0 for heterocyclics and 1 for benzene derivatives). Calculations indicated that PBD-coated alumina behaves as an RP stationary phase, the bulkiness and the polarity of the solute significantly influencing the retention. The separation efficiency of PBD-coated alumina was compared with those of other stationary phases for the analysis of Catharanthus alkaloids. It was established that the pH of the mobile phase, the concentration and type of the organic modifier, and the presence of salt simultaneously influence the retention. In this special case, the efficiency of PBD-coated alumina was inferior to that of ODS. The retention characteristics of polyethylene-coated alumina (PE-Alu) have been studied in detail using various nonionic surfactants as model compounds.It was found that PE-Alu behaves as an RP stationary phase and separates the surfactants according to the character of the hydrophobic moiety. The relationship between the physicochemical descriptors of 25 aromatic solutes and their retention on PE-coated silica (PE-Si) and PE-Alu was elucidated by stepwise regression analysis. [Pg.121]


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