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High stationary phases

Pink diatomaceous materials derived from crushed firebrick, for example, Chromosorb P. The material is used for high performance stationary phases due to its high surface area (4.0m g ) and support for high stationary phase loadings, up to 35% (w/w). It is particularly suitable for alkanes but must be deactivated by silanisation for polar compounds. [Pg.176]

Starting from the observations that at a high stationary phase percentage the film tliic.kness does not affect Tg and that the adsorption calculated from extrapolation of retention data at temperatures below Tg is smaller than the variation of retention volume with stationary phase percentage, Lipatov and Nesterov concluded that the increase of retention volume above Tg for films of intermediate thickness is due not to adsorption but to the less compact structure of thin layers. For thinnest films yielded by adsorption from solution they postulate the existence of adsorption at polymer-gas and polymer-support interfaces. The Tj increase for... [Pg.189]

Low salt concentrations result in a high stationary phase capacity (better development of the displacement train, which is a function of the stationary phase capacity). [Pg.82]

A tail at the end of a chromatographic peak, usually due to the presence of highly active sites in the stationary phase. [Pg.555]

Another important characteristic of a gas chromatographic column is the thickness of the stationary phase. As shown in equation 12.25, separation efficiency improves with thinner films. The most common film thickness is 0.25 pm. Thicker films are used for highly volatile solutes, such as gases, because they have a greater capacity for retaining such solutes. Thinner films are used when separating solutes of low volatility, such as steroids. [Pg.567]

Capillary Electrochromatography Another approach to separating neutral species is capillary electrochromatography (CEC). In this technique the capillary tubing is packed with 1.5-3-pm silica particles coated with a bonded, nonpolar stationary phase. Neutral species separate based on their ability to partition between the stationary phase and the buffer solution (which, due to electroosmotic flow, is the mobile phase). Separations are similar to the analogous HPLC separation, but without the need for high-pressure pumps, furthermore, efficiency in CEC is better than in HPLC, with shorter analysis times. [Pg.607]

Hydrophobic Interaction Chromatography. Hydrophobic interactions of solutes with a stationary phase result in thek adsorption on neutral or mildly hydrophobic stationary phases. The solutes are adsorbed at a high salt concentration, and then desorbed in order of increasing surface hydrophobicity, in a decreasing kosmotrope gradient. This characteristic follows the order of the lyotropic series for the anions ... [Pg.55]

Thin-Layer Chromatography. Chiral stationary phases have been used less extensively in tic as in high performance Hquid chromatography (hplc). This may, in large part, be due to lack of avakabiHty. The cost of many chiral selectors, as well as the accessibiHty and success of chiral additives, may have inhibited widespread commerciali2ation. Usually, nondestmctive visuali2ation of the sample spots in tic is accompHshed using iodine vapor, uv or fluorescence. However, the presence of the chiral selector in the stationary phase can mask the analyte and interfere with detection (43). [Pg.62]

High Performance Liquid Chromatography. Although chiral mobile phase additives have been used in high performance Hquid chromatography (hplc), the large amounts of solvent, thus chiral mobile phase additive, required to pre-equiUbrate the stationary phase renders this approach much less attractive than for dc and is not discussed here. [Pg.63]

Gyclodextrins. As indicated previously, the native cyclodextrins, which are thermally stable, have been used extensively in Hquid chromatographic chiral separations, but their utihty in gc appHcations was hampered because their highly crystallinity and insolubiUty in most organic solvents made them difficult to formulate into a gc stationary phase. However, some functionali2ed cyclodextrins form viscous oils suitable for gc stationary-phase coatings and have been used either neat or diluted in a polysiloxane polymer as chiral stationary phases for gc (119). Some of the derivati2ed cyclodextrins which have been adapted to gc phases are 3-0-acetyl-2,6-di-0-pentyl, 3-0-butyryl-2,6-di-0-pentyl,... [Pg.70]

Analytically, the inclusion phenomenon has been used in chromatography both for the separation of ions and molecules, in Hquid and gas phase (1,79,170,171). Peralkylated cyclodextrins enjoy high popularity as the active component of hplc and gc stationary phases efficient in the optical separation of chiral compounds (57,172). Chromatographic isotope separations have also been shown to occur with the help of Werner clathrates and crown complexes (79,173). [Pg.75]

Ca.rhora.nes, These are used in neutron capture therapy (254), and as bum rate modifiers in gun and rocket propellants. They are used as high temperature elastomers and other unique materials, high temperature gas—Hquid chromatography stationary phases, optical switching devises (256), and gasoline additives (257). [Pg.254]


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See also in sourсe #XX -- [ Pg.64 , Pg.80 ]




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