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  • 1
    Electronic Resource
    Electronic Resource
    Hoboken, NJ : Wiley-Blackwell
    AIChE Journal 41 (1995), S. 1602-1604 
    ISSN: 0001-1541
    Keywords: Chemistry ; Chemical Engineering
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Process Engineering, Biotechnology, Nutrition Technology
    Additional Material: 5 Ill.
    Type of Medium: Electronic Resource
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  • 2
    Electronic Resource
    Electronic Resource
    Weinheim : Wiley-Blackwell
    Macromolecular Rapid Communications 18 (1997), S. 921-925 
    ISSN: 1022-1336
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: A series of 2,3-O-carboxymethylcelluloses (CMC's), which are regioselectively substituted at the C-2 and C-3 position, were prepared and their water solubility was examined. It was found that the lower limit for the degree of substitution (DS) value of water-soluble 2,3-O-CMC is about 0.3. This value was almost the same as that of CMC prepared in a slurry of isopropyl alcohol/water with isopropyl chloroacetate and sodium hydroxide, showing that the uniform alkylation is rather important to convert cellulose into water-soluble derivatives.
    Additional Material: 1 Ill.
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  • 3
    Electronic Resource
    Electronic Resource
    Weinheim : Wiley-Blackwell
    Electroanalysis 2 (1990), S. 133-137 
    ISSN: 1040-0397
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Flow-injection analysis (FIA) with voltammetric detection can be used in either the direct voltammetric or the stripping mode. In this study, a locally designed and constructed instrument with features not available in commercial instruments was used for the precise analysis of silver in aluminum. The carrier solution was 0.1 M Al(NO3)3 with 2 × 10-3 M HNO3. Silver solution was introduced by timed, partial-loop injection. After cathodic deposition, a square-wave or staircase voltammetric stripping sweep was applied. The data were recorded and analyzed by computer. Silver solutions of 8 × 10-8 to 4 × 10-5 M were tested. The standard deviations of repeat determinations of artificial samples varied from 0.12 to 0.78%. This precision was limited by the stability of the pump flow.
    Additional Material: 4 Ill.
    Type of Medium: Electronic Resource
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  • 4
    Electronic Resource
    Electronic Resource
    Weinheim : Wiley-Blackwell
    Electroanalysis 2 (1990), S. 289-292 
    ISSN: 1040-0397
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Human immunoglobulin G and A (IgG and IgA) were studied with square-wave voltammetry. For IgG, three reduction peaks (HIGG1, HIGG2, and HIGG3) were observed under different conditions. HIGG1 and HIGG3 are strongly related to the pH of the buffer solution. In pH 7.5 phosphate buffer, the peak potential of HIGG2 is -0.58 V (vs. Ag/AgCl). A linear response holds for human IgG below 3.3 × 10-8 M (5 ppm). As little as 1.1 × 10-10 M (16 ppb) of human IgG is detectable after only 20 seconds of adsorptive accumulation in static solution.IgA has two flat adsorptive-stripping responses (HIGA1 and HIGA2). The sensitivity of IgA is much poorer compared to IgG. HIGA2 at -0.44 V can be observed throughout the tested pH range with the maximum response between pH 6.0-6.2. In a static solution, a linear calibration graph can be obtained for 0.8-16.8 ppm IgA.IgG and IgA can be separated from each other by using HPLC with an AB × column. The response of 32 ppb IgG can be observed clearly. This research indicates the possibility of direct separation and detection of immunoglobulins from a real sample (e.g., human serum) by simply applying HPLC-adsorptive-stripping analysis.
    Additional Material: 4 Ill.
    Type of Medium: Electronic Resource
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