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  • 1
    ISSN: 0935-6304
    Keywords: Capillary GC ; On-line extractive alkylation ; On-line acylation ; Carboxylic acids ; Amines ; Chemistry ; Analytical Chemistry and Spectroscopy
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Gas chromatographic procedures are described for the determination of carboxylic acids and chlorinated anilines in water samples.Propionic acid and 2,6-difluorobenzoic acid in aqueous solution have been simultaneously alkylated and extracted by means of a continuous two-phase reaction system, and then quantitated by on-line coupled capillary gas chromatography; tetrahexyl-ammonium hydrogen sulfate was used as phase transfer catalyst and pentafluorobenzyl bromide as reagent.A factorial design approach was used to optimize on-line derivatization of aqueous propionic acid with regard to pH and concentration of phase transfer catalyst. Alkylation and extraction, under optimized conditions, followed by quantitation of the pentafluorobenzyl ester by flame ionization detection furnished a linear calibration for concentrations between 0.1 and 10 μg/ml. The relative standard deviation was 9-15 %.The continuous two-phase reaction system was also used to determine (chlorinated) anilines present in water at concentrations of 0.1-1 μg/ml; pentafluorobenzoyl chloride was used as reagent and analysis was performed by capillary gas chromatography with flame ionization or electron capture detection. The on-line acylation of p-chloroaniline was optimized with regard to pH, reagent concentration, and reaction time.The on-line reaction system worked satisfactorily for both applications, although excess reagent caused some problems with the chromatography.
    Additional Material: 6 Ill.
    Type of Medium: Electronic Resource
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  • 2
    ISSN: 0935-6304
    Keywords: On-line extraction ; Large volume introduction ; Capillary gas chromatography ; Atomic emission detection ; Solvent venting ; Pesticides ; Ground water ; Chemistry ; Analytical Chemistry and Spectroscopy
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The on-line coupling of a liquid-liquid extraction system with capillary gas chromatography using atomic emission detection (GC-AED) has been studied. The required large volumes of about 100 μl of an iso-octane solution can be introduced into the GC-AED system by using the AED solvent vent and a solvent vapor exit in front of the capillary analytical column. Test solutions containing several pesticides were detected using the carbon, chlorine, nitrogen and sulfur channels. Analyte detectability (in concentration units) was improved significantly and low concentractions of the test compounds could be determined (1-5 ng/ml). Aqueous samples were on-line extracted and analyzed. The precision of the large-volume injection itself as well as the total extraction-GC-AED system was satisfactory (RSD of ca. 2 and 4%, respectively). As a real-life application, several ground water samples were screened.
    Additional Material: 6 Ill.
    Type of Medium: Electronic Resource
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  • 3
    ISSN: 1040-7685
    Keywords: capillary GC ; reversed-phase LC ; on-line coupling ; solvent vapor exit ; pressure-balanced carrier gas system ; Chemistry ; Analytical Chemistry and Spectroscopy
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: A large-volume introduction system for capillary gas chromatography (GC) is described which can be coupled on-line with reversed-phase liquid chromatography (LC) using 2 mm i.d. LC columns. An on-column interface with a special retention gap, coated with a very thin film (0.02 μm) of Carbowax was used. Insertion of a solvent vapor exit before the analytical gas chromatography column allowed the solvent evaporation rate for an azeotropic acetonitrile/water mixture (84:16, v/v) to increase from 20 to 175 μL min-1 at 91°C and 150 kPa inlet pressure. A volume of 200 μL of this mixture containing phenanthrene and the potential basic drug eltoprazine, could be injected into the retention gap at introduction rates up to 200 μL min-1, under partially concurrent solvent evaporation conditions. Repeatability (CV = 2.4%) and linearity (at least 10-1000 ng mL-1) were satisfactory. The Carbowax-coated retention gap has a relatively large retention power for the polar solute. This means that the solvent can be completely evaporated through the vapor exit without loss of analyte. With apolar solutes, losses will occur if evaporation is unduly prolonged. In order to allow the use of a nitrogen-phosphorus detector, a special pressure-balanced carrier gas circuit was designed and tested for total solvent-free performance of the detector. With this set-up, 150 μL injections of eltoprazine in the acetonitrile/water azeotrope were made at an introduction rate of 200 μL min-1. No traces of acetonitrile were detected, while analyte detectability was 20-fold higher than with the FID.Finally, the practicability of reversed-phase LC-GC was demonstrated by on-line heart-cutting of the phenanthrene-containing fraction from a 2 mm i.d. LC column using acetonitrile/water (84:16, v/v) as eluent, and analyzing it by capillary GC-FID.
    Additional Material: 6 Ill.
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  • 4
    ISSN: 0935-6304
    Keywords: Capillary GC ; Continuous liquid-liquid extraction ; Environmental applications ; Chemistry ; Analytical Chemistry and Spectroscopy
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The applicability of a liquid-liquid extraction system which is coupled on-line with a capillary gas chromatograph was studied for environmental and ecotoxicological analyses. The optimized and automated system was used for the determination of apolar and rather non-volatile organic compounds in aqueous samples. Relevant aspects of sample introduction, phase separation and selection of extraction solvent are discussed. Three routine-tipe applications are described, viz. an improved method for the determination of hexachlorocyclohexanes in ground water and the determination of the so-called NCC-ether and ACC-ether in ecotoxicological studies. Depending on the application studied, the concentration levels varied from 0.1 to 6000 μg/I, using ECD and/or FID detection. Typical coefficients of variation obtained with the total extraction-GC procedure were 2-25%.The system was found to be rugged, it saves time compared with set-ups involving off-line liquid-liquid extraction and considerably reduces the manual work load.
    Additional Material: 6 Ill.
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  • 5
    Electronic Resource
    Electronic Resource
    Weinheim : Wiley-Blackwell
    Journal of High Resolution Chromatography 22 (1999), S. 495-500 
    ISSN: 0935-6304
    Keywords: CZE ; mobility ratio ; migration time prediction ; mathematical model ; Chemistry ; Analytical Chemistry and Spectroscopy
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: ---The electrophoretic mobility ratio (R value) of any two ions is constant and independent of the capillary type and electrophoretic conditions if their electrical charges and hydration radii are constant. The use of strong acid salts and quaternary ammonium salts is therefore proposed for the determination of R values. Such analytes are called markers. The following determinations can be carried out: (i) the determination of the migration time corresponding to the electroosmotic flow (EOF) in any capillary under any electrophoretic condition by measuring the migration times of two markers in the condition studied (useful when the EOF is weak); (ii) the determination of the migration time of an analyte in any capillary by knowing the migration time of the markers in the capillary studied. If the pH is changed and the ionization of the analyte is pH dependent, the resulting migration time for the analyte can be calculated. The constancy of the mobility ratios of seven markers was checked experimentally at eight different pH values (between pH 3 and 10), at three temperatures, and for two buffer concentrations. The predicted and experimental migration times were also compared in two different types of capillaries.
    Additional Material: 2 Ill.
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  • 6
    Publication Date: 2019-07-13
    Description: The ultraviolet (1150 - 2850 A) spectra of a number of active galactic nuclei (AGNs) observed with the Hubble Space Telescope (HST) Faint Object Spectrograph (FOS) have been used to study the properties of the Galactic halo. The objects that served as probes are 3C 273, PKS 0454-220, Pg 1211+143, CSO 251, Ton 951, and PG 1351+640. The equivalent widths of certain interstellar ions have been measured, with special attention paid to the C IV/C II and Si IV/Si II ratios. These ratios have been intercompared, and the highest values are found in the direction of 3C 273, where C IV/C II = 1.2 and Si IV/Si II greater than 1. These high ratios may be due to a nearby supernova remnant, rather than to ionized gas higher up in the Galactic halo. Our data give some support to the notion that QSO metal-line systems may arise from intervening galaxies which contain high supernova rates, galactic fountains, and turbulent mixing layers.
    Keywords: ASTRONOMY
    Type: Astrophysical Journal, Part 1 (ISSN 0004-637X); 437; 2; p. 630-637
    Format: text
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  • 7
    Publication Date: 2019-08-27
    Description: Hubble Space Telescope (HST) Faint Object Spectrograph (FOS) spectra are presented for three bright Seyfert galaxies including one (PG 1351+64) which possesses blue-displaced absorption features in C IV, Si IV, N V, and Ly-alpha (but not in Mg II) similar to those seen at high redshift in the broad-absorption-line (BAL) quasi-stellar objects (QSOs). Several features of the absorptions in PG 1351+64, including variability seen in archival International Ultraviolet Explorer (IUE) data, confirm their similarity to the BAL clouds rather than to the 'associated absorber' phenomenon which they superficially resemble. In PG 1351+64 'satellite' emission lines (called herein E1 and E2) have been detected nearly symmetrically placed at +/- 4000 km/s around the Mg II emission line; this velocity is just larger than the most blue-displaced of the BALs, suggesting that these two phenomena are related. The satellite line luminosity, L(E1) approximately = (3 x 10(exp 41) erg/s)/sq. h(sub 75), requires a cloud emission measure n(sub e)(exp 2)V(sub c) approximately = (1 x 10(exp 64)/cc)/sq. h(sub 75) at T approximately = 30,000 K. We believe the Mg II lines are produced by 50-90 km/s shocks driven into dense (approximately 10(exp 6)/cc, pre-shock) clouds by the ram pressure of a 0.1 solar mass/yr wind leaving the nucleus at velocity 4000 km/s. The detection of satellite lines in Mg II, the detection of the blue-shifted cloud in H-alpha and H-beta and the nondetection of this cloud in C IV restricts the cloud shocks to velocities v(sub c) less than or = 90 km/s and requires a cloud/wind density contrast greater than or = 10(exp 3). In this model, the emitting clouds are located at distances of R(sub eff) approximately = 10(exp 18-19) cm from the nucleus and are entrained and shock-accelerated to approximately 4000 km/s. The possible detection of similar 'satellite' emission features in the non-BAL Seyfert, Ton 951, suggests that the subrelativistic wind that accelerates BAL clouds is a physical feature of many radio-quiet active galactic nuclei (AGN).
    Keywords: ASTRONOMY
    Type: The Astronomical Journal (ISSN 0004-6256); 108; 4; p. 1178-1185
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