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  • 1
    Electronic Resource
    Electronic Resource
    s.l. : American Chemical Society
    Journal of the American Chemical Society 100 (1978), S. 6128-6132 
    ISSN: 1520-5126
    Source: ACS Legacy Archives
    Topics: Chemistry and Pharmacology
    Type of Medium: Electronic Resource
    Library Location Call Number Volume/Issue/Year Availability
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  • 2
    Electronic Resource
    Electronic Resource
    New York, NY : Wiley-Blackwell
    International Journal of Chemical Kinetics 27 (1995), S. 1055-1064 
    ISSN: 0538-8066
    Keywords: Chemistry ; Physical Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The oxidation kinetics of malic acid by vanadium(V) in aqueous sulphuric acid was investigated at 303 K by monitoring the appearance of vanadium(IV) at 760 nm. The reaction showed first-order behavior with respect to vanadium(V), malic acid, and hydrogen ion concentration, respectively, regardless of the ionic strength. The reaction rate is enhanced by an increase in ionic strength and a decrease of the dielectric constant of the medium by addition of methanol. The activation parameters were estimated by varying the temperature in the range of 293 K to 313 K to 313 K. An oxidation mechanism is proposed, involving different vanadium(V) species produced in the presence of sulphuric acid. © 1995 John Wiley & Sons, Inc.
    Additional Material: 2 Ill.
    Type of Medium: Electronic Resource
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  • 3
    Electronic Resource
    Electronic Resource
    New York, NY : Wiley-Blackwell
    International Journal of Chemical Kinetics 30 (1998), S. 55-61 
    ISSN: 0538-8066
    Keywords: Chemistry ; Physical Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Tartaric acid oxidation by vanadium(V) in sulfuric acid medium was investigated spectrophotometrically at 760 nm and 30°C by appearance of the vanadium(IV), as vanadyl. The reaction rate was determined under pseudo-first-order conditions with an excess of hydroxyacid over the oxidant concentration. The oxidation showed a first-order dependence with respect to vanadium(V) concentration and fractional orders with respect to tartaric acid and sulfuric acid concentrations, with no control and with constant ionic strength. The reaction rate is enhanced by an increase of ionic strength, and slightly reduced by a decrease of the dielectric constant of the medium. The activation parameters were calculated based on the rate constants determined in the 293 to 313 K interval. The proposed oxidation mechanisms and the derived rate laws are consistent with the experimental rate laws. © 1998 John Wiley & Sons, Inc. Int J Chem Kinet: 30: 55-61, 1998.
    Additional Material: 2 Ill.
    Type of Medium: Electronic Resource
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