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  • 1
    Electronic Resource
    Electronic Resource
    s.l. : American Chemical Society
    Analytical chemistry 58 (1986), S. 2663-2668 
    ISSN: 1520-6882
    Source: ACS Legacy Archives
    Topics: Chemistry and Pharmacology
    Type of Medium: Electronic Resource
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  • 2
    Electronic Resource
    Electronic Resource
    s.l. : American Chemical Society
    The @journal of physical chemistry 〈Washington, DC〉 89 (1985), S. 2571-2576 
    Source: ACS Legacy Archives
    Topics: Chemistry and Pharmacology , Physics
    Type of Medium: Electronic Resource
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  • 3
    Electronic Resource
    Electronic Resource
    Springer
    Chromatographia 8 (1975), S. 60-66 
    ISSN: 1612-1112
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology
    Notes: Summary A suitable criterion of performance for a production chromatograph is the total separation cost, including capital and operating costs, per unit mass of product. A semi-empirical expression for this parameter is developed for gas-liquid chromatography. The equation is used to find the effect of chromatographic design and operating variables on performance and, where relevant, to find the optimum values of these variables. Optimum values exist for feed band width, column length, degree of band overlap and column temperature. In general, the carrier velocity and feed concentration should be as high as possible and the theoretical plate height as low as possible. The stationary phase loading has only a small, if any, net effect on performance. The stationary phase should be chosen for its chemical stability, involatility and enhancement of solute relative volatility.
    Type of Medium: Electronic Resource
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  • 4
    Electronic Resource
    Electronic Resource
    Springer
    Chromatographia 7 (1974), S. 387-394 
    ISSN: 1612-1112
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology
    Notes: Summary This paper surveys gas chromatographic methods for making thermodynamic measurements at finite solute concentration. The factors which determine the shape of elution and frontal chromatograms are first described. The retention volume equation is obtained for finite concentration taking into account the sorption effect and curvature of the distribution isotherm. A new and reasonably accurate equation (Equation 20) is then derived for calculation of the isotherm from chromatographic measurements. Comparison is made with an older, much used procedure which is shown to give large errors through neglecting the sorption effect. Experimental results with both accurate and inaccurate procedures are surveyed.
    Type of Medium: Electronic Resource
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  • 5
    Electronic Resource
    Electronic Resource
    Springer
    Chromatographia 16 (1982), S. 44-47 
    ISSN: 1612-1112
    Keywords: Production gas chromatography ; Design of equipment ; Heat-sensitive essential oils
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology
    Notes: Summary A rational design procedure for production and preparative chromatography has previously been devised. Here the procedure is applied to designing a pilot scale production gas chromatograph for separating two heatsensitive essential oil mixtures: geraniol/nerol and α-/β-pinenes. Analytical scale experiments provide some of the data required. A critical feature of the design is that these materials degrade at temperatures well below their boiling points. The design study leads, first, to selection of carrier gas, stationary phase and solid support materials, and then to quantitative determination of column temperature, evaporator temperature, feed concentration in the carrier gas, column diameter, particle size of support, carrier velocity, ratio of recycled to inject feed, injection time, column length, and liquid phase loading.
    Type of Medium: Electronic Resource
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  • 6
    Electronic Resource
    Electronic Resource
    Weinheim : Wiley-Blackwell
    Journal of High Resolution Chromatography 5 (1982), S. 341-348 
    ISSN: 0935-6304
    Keywords: Chemistry ; Analytical Chemistry and Spectroscopy
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Asymmetrical or tailed peaks are a common problem in chromatography. The causes of this distortion are described and classified. Each case is discussed from the point of view of first diagnosing the cause of asymmetry end then dealing with it appropriately; e.g. by removing the cause or, in applications to physicochemical measurement, by using more appropriate measures of retention than the residence time of the peak maximum. The classification of sources of asymmetry applies to both gas and liquid chromatography, allowing information derived from one field to be extended to the other.Part 1 of this review covers nonlinear, concentration-dependent behavior with and without nonideal band-spreading. Part 2 will deal with sources of distortion controlled by the kinetics of transport or reaction processes, viz. apparatus effects, incomplete resolution, slow kinetic processes, chemical reaction, and column voids.
    Additional Material: 5 Ill.
    Type of Medium: Electronic Resource
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  • 7
    Electronic Resource
    Electronic Resource
    Weinheim : Wiley-Blackwell
    Journal of High Resolution Chromatography 12 (1989), S. 407-407 
    ISSN: 0935-6304
    Keywords: Chemistry ; Analytical Chemistry and Spectroscopy
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Type of Medium: Electronic Resource
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  • 8
    Electronic Resource
    Electronic Resource
    Weinheim : Wiley-Blackwell
    Journal of High Resolution Chromatography 5 (1982), S. 397-403 
    ISSN: 0935-6304
    Keywords: Chemistry ; Analytical Chemistry and Spectroscopy
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The review of the characterization, diagnosis, and treatment of peak distortion begun in Part 1 is concluded. Part 1 dealt with peak distortion caused by nonlinear (concentration-dependent) chromatographic behavior in the column. The present part covers peak distortion due to either the apparatus, incomplete resolution, slow kinetic processes, reaction on the column, or column voids. All these sources are controlled by the kinetics of transport or reaction processes.
    Additional Material: 6 Ill.
    Type of Medium: Electronic Resource
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  • 9
    Electronic Resource
    Electronic Resource
    Weinheim : Wiley-Blackwell
    Journal of High Resolution Chromatography 7 (1984), S. 615-619 
    ISSN: 0935-6304
    Keywords: Theory ; Sorption ; Plate model ; Band widths ; Chemistry ; Analytical Chemistry and Spectroscopy
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The original plate model of chromatography is extended to the sorption process occurring at the column inlet and the desorption process at the column exit. At the column inlet it is shown that sufficiently wide feed bands undergo no change in concentration but a fall in band width, i.e., the volume of mobile phase occupied by the solute band is reduced. The reduction factor is (1 + k) where k is the mass distribution ratio (capacity factor). Narrower bands suffer partial reduction in both band width and concentration. On desorption at the outlet, however, the change is always in band width and not concentration. A perfect detector registers the true concentration-time profile of the band in the column if the solute mass fraction in the stationary phase is below 10-3 at the column outlet. The risks of stripping the stationary phase at high solute concentrations in analytical and preparative or production gas chromatography are compared.
    Additional Material: 4 Ill.
    Type of Medium: Electronic Resource
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  • 10
    Publication Date: 1985-06-01
    Print ISSN: 0022-3654
    Electronic ISSN: 1541-5740
    Topics: Chemistry and Pharmacology , Physics
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