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Temperature-programmed chromatography

Initial and final temperatures. The temperature range used for a separation in temperature-programmed chromatography. [Pg.25]

Fig. 1.12 Temperature-programmed chromatography of oxides [46], Conditions quartz column, length 100 cm, 8 mm i.d, filled with quartz granules 0,32-0.63 mm heating rate 20 K min-1 carrier gas and reagent oxygen, 3 cm3 min-1. Fig. 1.12 Temperature-programmed chromatography of oxides [46], Conditions quartz column, length 100 cm, 8 mm i.d, filled with quartz granules 0,32-0.63 mm heating rate 20 K min-1 carrier gas and reagent oxygen, 3 cm3 min-1.
Rudolph and Bachmann [90,91] studied in detail isothermal chromatography of chlorides of several fission products. They used quartz columns filled with graphite, quartz or quartz coated with NaCl, KC1, MgCl2 or CsCl. They made careful measurements of the retention time versus column temperature, and of the peak widths. The best separation was achieved by temperature-programmed chromatography. It is illustrated by Fig. 1.23. [Pg.30]

Van Den Dool, H. and P.D. Kratz (1963), Generalization of the retention index system including linear temperature programmed gas-liquid partition chromatography . J. Chromatogr, Vol. 11, p. 463. [Pg.460]

Figure 12.22 SFC-GC analysis of aromatic fraction of a gasoline fuel, (a) SFC trace (b) GC ttace of the aromatic cut. SFC conditions four columns (4.6 mm i.d.) in series (silica, silver-loaded silica, cation-exchange silica, amino-silica) 50 °C 2850 psi CO2 mobile phase at 2.5 niL/min FID detection. GC conditions methyl silicone column (50 m X 0.2 mm i.d.) injector split ratio, 80 1 injector temperature, 250 °C earner gas helium temperature programmed, — 50 °C (8 min) to 320 °C at a rate of 5 °C/min FID detection. Reprinted from Journal of Liquid Chromatography, 5, P. A. Peaden and M. L. Lee, Supercritical fluid chromatography methods and principles , pp. 179-221, 1987, by courtesy of Marcel Dekker Inc. Figure 12.22 SFC-GC analysis of aromatic fraction of a gasoline fuel, (a) SFC trace (b) GC ttace of the aromatic cut. SFC conditions four columns (4.6 mm i.d.) in series (silica, silver-loaded silica, cation-exchange silica, amino-silica) 50 °C 2850 psi CO2 mobile phase at 2.5 niL/min FID detection. GC conditions methyl silicone column (50 m X 0.2 mm i.d.) injector split ratio, 80 1 injector temperature, 250 °C earner gas helium temperature programmed, — 50 °C (8 min) to 320 °C at a rate of 5 °C/min FID detection. Reprinted from Journal of Liquid Chromatography, 5, P. A. Peaden and M. L. Lee, Supercritical fluid chromatography methods and principles , pp. 179-221, 1987, by courtesy of Marcel Dekker Inc.
The above consequences of isothermal operation may be largely avoided by using the technique of programmed-temperature gas chromatography (PTGC) in which the temperature of the whole column is raised during the sample analysis. [Pg.245]

W E Harris and H W Habgood, Programmed Temperature Gas Chromatography, Wiley, New York, 1966... [Pg.253]

The purity of 1 and 2 is assessed by analytical gas-liquid chromatography (GC) on a Hewlett-Packard 5890 gas chromatograph equipped with a flame-ionization detector and fitted with a 50 m x 0.2 mm HP-5 fused silica glass capillary column using linear temperature programming from an initial temperature of 150°C for 5 min to a final temperature of 200°C for 10 min at a rate of 5°C/min. [Pg.64]

Chromatography Hewlett-Packard Ultra2 (25 m x 0.33 mm) cross-linked phenyl methyl silicone fused silica capillary column. Temperature program 55° (1 min.) -I- 30°C/min. to 180°C, and 4°C/min. to 320°C. [Pg.253]

Jaglan PS, Gunther FA. 1970. Single column gas liquid chromatography of methyl parathion and metabolites using temperature programming. Bull Environ Contam Toxicol 5 111-114. [Pg.214]

Marutoiu C, Sarbu C, Vlassa M, et al. 1986. A new separation and identification method of some organophosphorus pesticide by means of temperature programming gradient thin-layer chromatography. Analysis 14 95-98. [Pg.221]

Halang, W. A., Langlais, R., and Kugler, E., Cubic Spline Interpolation for the Calculation of Retention Indices in Temperature-Programmed Gas-Liquid Chromatography, Ana/. Chem. 50, 1978, 1829-1832. [Pg.412]

The gases used were purchased premixed in aluminum cylinders to avoid carbonyl formation. The high purity gas mixture was further purified by a zeolite water trap and a copper carbonyl trap. The gas pressure in the reactor was measured with a capci-tance manometer and the fTow monitored with a mass fTow controT-ler. The typical gas flow rates were 15 cc/min (STP) and the maximum conversion was 1% based on integration of hydrocarbon products. The hydrocarbon products were analyzed by gas chromatography (temperature programmed chromosorb 102, FID). [Pg.125]

The separation nuaber is the only column efficiency par2uaeter that can be deterained under teaperature progr2uued conditions [45,46]. The critical parameters that aust be standardized to obtain reproducible SM values for coluans of different length are the carrier gas flow rate and the temperature program. The SN is widely used as part of a standardized test method to evaluate the quality of open tubular columns for gas chromatography (section 2.4.3). [Pg.12]

The temperature program mode is the most widely used separation technique in gas chromatography [155]. As well as reducing separation times for samples with a wide tailing point... [Pg.31]

Chiu, G., Separation of carboxylic acids by temperature programmed liquid chromatography, /. HRC CC, 9, 410, 1986. [Pg.276]


See other pages where Temperature-programmed chromatography is mentioned: [Pg.138]    [Pg.49]    [Pg.125]    [Pg.127]    [Pg.240]    [Pg.15]    [Pg.289]    [Pg.138]    [Pg.49]    [Pg.125]    [Pg.127]    [Pg.240]    [Pg.15]    [Pg.289]    [Pg.558]    [Pg.143]    [Pg.402]    [Pg.244]    [Pg.245]    [Pg.346]    [Pg.318]    [Pg.16]    [Pg.32]    [Pg.33]    [Pg.104]    [Pg.123]    [Pg.515]    [Pg.516]    [Pg.551]    [Pg.552]    [Pg.573]    [Pg.185]    [Pg.187]    [Pg.233]    [Pg.243]    [Pg.252]   


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