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Liquid chromatography supercritical fluid chromatograph

Chromatography. GC is the most common anal)d ical method used but liquid and supercritical fluid chromatographic methods are being increasingly developed. Like titration the sample is destroyed in the analysis process. The ideal situation depicted in Figure 8.8 cannot normally be applied for titration or chromatographic analysis since the analysis equipment needs to be close to the sampling device. This is often termed at-line analysis. [Pg.256]

In addition to conventional liquid chromatography, supercritical fluid chromatography (SFC), using a supercritical fluid as mobile phase (mostly scf-C02), has attracted attention in the last decades [58, 164, 168, 169]. Supercritical fluids provide a favourable medium for the transport of solutes through a chromatographic column because they resemble a gas in terms of viscosity, a liquid in terms of density, and are intermediate between these two phases in terms of diffusivity. For some physieal properties of supercritical solvents, see Section 3.2. [Pg.494]

Among aU chromatographic techniques that can be applied for the separation and identification of polymer additives after the extraction step, high-temperature capillary gas chromatography (CGC), " high-performance liquid chromatography supercritical fluid chro-... [Pg.1864]

Most supercritical fluid chromatographs use carbon dioxide as the supercritical eluent, as it has a convenient critical point of 31.3°C and 72.5 atmospheres. Nitrous oxide, ammonia and n-pentane have also been used. This allows easy control of density between 0.2g ml-1 and 0.8g ml-1 and the utilization of almost any detector from liquid chromatography or gas chromatography. [Pg.58]

D. Tong, K. D. Bartle, A. A. Clifford and R. E. Robinson, Unified chromatograph for gas chromatography, supercritical fluid chromatography and micro-liquid chromatography, Analyst 120 2461 (1995). [Pg.16]

A very recent volume edited by Berthed (2002) is on countercurrent chromatography - the support-free liquid stationary phase. Ebdon et al. (1987) review directly coupled liquid chromatogramphy-atomic spectroscopy. The review by Uden (1995) on element-specific chromatographic detection by atomic absorption, plasma atomic emission and plasma mass spectrometry covers the principles and applications of contemporary methods of element selective chromatographic detection utilizing AA, AES and MS. Flame and furnace are considered for GC and HPLC, while MIP emission is considered for GC and ICPAES for HPLC. Combinations of GC and HPLC with both MIPAES and ICPAES are covered and supercritical fluid chromatographic (SFC) and field flow fractionation (FFF) are also considered. [Pg.1604]

Supercritical Fluid Chromatography (SFQ and Supercritical Fluid Extraction (SFE) A separation technology similar to other extraction and chromatographic methods, but in which the mobile phase is actually a fluid in its supercritical fluid state. A supercritical fluid is a fluid that is held above its critical temperature and pressure, and for which no application of additioncJ pressure can result in the development of a liquid phase. Supercritical fluids are unique in that while they possess liquid-like densities, the mass transfer behavior is superior to that of liquids. Supercritical fluid chromatography remains a niche method that is applicable to pharmaceuticals and other high relative molecular mass solutes. Supercritical extraction, on the other hand, is more widely used as a sample preparation method, especially in pharmaceutical analyses, polymers, and environmental analyses. [Pg.1416]


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