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61.
Summary In this work, an optimization procedure for gradient RPLC separation, using ternary mobile phases, is described. This procedure requires eight preliminary experiments in gradient elution mode to predict the retention surface for each solute over the whole triangular space. This is followed by computerized calculations to determine the best ternary gradient elution profile with respect to both selectivity and analysis time. The efficiency of this procedure from the point of view of rapidity and of accuracy, is illustrated for the specific separation of twelve phenyl urea herbicides. 相似文献
62.
Sameena Ashraf Keith D. Bartle Anthony A. Clifford Robert Moulder 《Journal of separation science》1992,15(8):535-538
Lubricating oil additives have been analyzed by supercritical fluid chromatography on open tubular and packed capillary columns. Carbon dioxide and modified carbon dioxide were used as mobile phases and detection was accomplished by flame ionization and micro UV. Rapid and efficient analysis of the lubricating oil additives was demonstrated. 相似文献
63.
This paper describes the theory of liquid adsorption chromatography (LSC) with mixed mobile phase, involving formation of multilayer surface phases. An equation describing the dependence of the capacity ratio upon the mobile phase composition is derived and theoretical curves illustrating the same dependence are calculated accordingly by assuming different thicknesses of the surface phase. 相似文献
64.
An indirect UV photometric detection technique is described in which a low concentration of a UV-absorbing compound (UVAC) is added to the mobile phase in reversed phase liquid chromatography, thereby making it possible for non UV-absorbing compounds such as the lower alcohols to be detected by the UV detector. This happens because the injected analyte may extract a portion of the UV absorbing compound from the mobile and/or stationary phase and the complex is co-eluted as a positive peak at the retention time of the analyte. Alternatively, the injected analyte may appear as a negative peak if the UV-absorbing compound is transferred to the mobile and stationary phases. In any case, the injected compound appears either as a positive or negative peak depending on the relative polarities and concentrations of all the compounds in the system. In addition, the resulting excess or deficiency of detection agent in the stationary phase is eluted separately as a positive or negative peak, indicating that the system has returned to equilibrium. In the work described herein, the chromatographic conditions and variables of the indirect photometric technique were studied to develop a quantitative HPLC method for UV-transparent compounds. It was found that under optimal conditions it is possible to determine some analytes quantitatively at concentrations as low as 0.05%. 相似文献
65.
T. Kowalska 《Chromatographia》1991,31(3-4):119-122
Summary Intermolecular interactions between the solute and the moieties constituting the mobile phase significantly contribute to the overall retention pattern of a given solute in a given chromatographic system. In this paper retention of solute is discussed in the case of the B+AB1+AB2 type mobile phase, which, in a quasithermodynamic way, can be divided into seven individual moieties. One evaluates the influence of each moiety on solute retention, and refers these regularities to the polarity of the solutes. 相似文献
66.
Summary Packings and stationary phases applied to high resolution separations of proteins, enzymes, and nucleic acids must satisfy
a series of distinct criteria that are different from those usually required by HPLC of low molecular weight non-biologically
active analytes. These requirements have been met through substantial improvements in classical gel media together with novel
developments in silica supports, and have led to a family of products with tailor-made and reproducible properties. Supports
consisting of cross-linked organic gels, and inorganic materials (mostly silicas) are now available with graduated particle
sizes, pore sizes, porosities and surface areas as well as non-porous beads. A whole range of stationary phases, such as reversed
phase, hydrophobic interaction, ion exchanger and affinity packings, were designed for application as chemical sensors for
biopolymer recognition in adsorptive chromatography. The phase systems are operated in the gradient mode, giving high resolution
and high peak capacities. In addition, aqueous liquid-liquid partitioning systems have been developed for the fractionation
of proteins and nucleic acids. Size exclusion media complete the set of HPLC variants enabling a discrimination of proteins
according to their size and shape in an isocratic elution mode. Basically, protein purification and isolation is a multistage
process where-by the HPLC variants are combined in a logistic sequence, utilizing the different selectivities of the phase
systems and thus maximising resolution, speed and throughput. 相似文献
67.
The method for the prediction of capacity factors in ternary mobile phases is presented. The adsorption mechanism of retention is considered. The simple theoretical equations are proposed for mobile phases for which the ratio of mole fractions of the weaker solvents remains fixed. The relations between parameters characterizing retention in ternary and binary mobile phases are discussed. The theoretical model is verified for numerous solutes and different mobile phases. 相似文献
68.
This paper concerns the application of excess adsorption isotherms, measured for solvent mixture/adsorbent systems, to the characterization of TLC data. For this purpose the excess adsorption isotherms for three liquid mixtures: cyclohexane/ benzene, benzene/acetone, and carbon tetrachloride/ethyl acetate on silica gel at 20°C have been measured. These mixtures have been used as binary mobile phases in TLC measurements. It has been shown for a given solute in binary mobile phase that the quantity RM is a simple function of the excess adsorption. Parameters of this function have been used to characterize chromatographic systems with binary mobile phases. 相似文献
69.
Reversed phase high performance liquid chromatography (RPLC) is currently the method of choice for the analysis of basic compounds. However, with traditional silica materials, secondary interactions between the analyte and residual silanols produce peak tailing which can negatively affect resolution, sensitivity, and reproducibility. In order to reduce these secondary interactions, which comprise ion exchange, hydrogen bonding, and London forces interactions, chromatographic analyses can be carried out at low or high pH values where silanol groups and basic compounds are mostly uncharged. The chromatographic behaviour of a particular bidentate stationary phase, Zorbax Extend C18, was studied with a set of basic and neutral compounds. Thanks to a higher chemical stability than traditional silica based supports, analyses were carried out with a high pH mobile phase, which represents a good alternative to the acidic mobile phases generally used to reduce ion exchange interactions. The performance of this bidentate stationary phase was also compared with that of other supports and it was proved that it is advantageous to work with high pH mobile phases when analyzing basic compounds. 相似文献
70.
The influence of a water vapor admixture in helium, nitrogen, and carbon dioxide on capacity coefficients of C3−C5 alcohols and pyridine during chromatography process in capillary columns with polar (PEG-20M) and nonpolar (SE-30) stationary
phases was studied. The introduction of a water admixture into the carrier gas, increases the capacity coefficient of polar
organic compounds on the capillary column with PEG-20M and has almost no effect on this value in the case of SE-30. The change
in retention of polar organic compounds on the capillary column with the PEG-20M polar phase occurs due to a change in the
properties of the stationary phase when it adsorbs water from the mobile phase.
Translated fromIzvestiya Akademii Nauk. Seriya Khimicheskaya, No. 11, pp. 2258–2261, November, 1998. 相似文献