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  • 1
    Electronic Resource
    Electronic Resource
    New York, NY : Wiley-Blackwell
    International Journal of Chemical Kinetics 30 (1998), S. 207-214 
    ISSN: 0538-8066
    Keywords: Chemistry ; Physical Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Manganese(II) is oxidized by ozone in acid solution, k=(1.5±0.2)×103 M-1 s-1 in HClO4 and k=(1.8±0.2)×103M-1 s-1 in H2SO4. The plausible mechanism is an oxygen atom transfer from O3 to Mn2+ producing the manganyl ion MnO2+, which subsequently reacts rapidly with Mn2+ to form Mn(III). No free OH radicals are involved in the mechanism. The spectrum of Mn(III) was obtained in the wave length range 200-310 nm. The activation energy for the initial reaction is 39.5 kJ/mol. Manganese(III) is reduced by hydrogen peroxide to Mn(II) with k(Mn(III)+H2O2)=2.8×103M-1 s-1 at pH 0-2. The mechanism of the reaction involving formation of the manganese(II)-superoxide complex and reaction of H2O2 with Mn(IV) species formed due to reversible disproportionation of Mn(III), is suggested. © 1998 John Wiley & Sons, Inc. Int J Chem Kinet 30: 207-214, 1998.
    Additional Material: 6 Ill.
    Type of Medium: Electronic Resource
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  • 2
    Electronic Resource
    Electronic Resource
    New York, NY : Wiley-Blackwell
    International Journal of Chemical Kinetics 30 (1998), S. 215-221 
    ISSN: 0538-8066
    Keywords: Chemistry ; Physical Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The lifetime of the ferryl ion FeO2+, (minutes at pH below 1) is reduced by a factor of 50 at pH above 3. This is rationalized in terms of an acid-base equilibrium between two different hydrolytic forms of this species (Fe(OH)++2 and Fe(OH)+3) with a pKa=2.0. The rate constants for reactions between FeO2+ and selected compounds found in cloud water were measured in acid solutions by stopped-flow technique. For inorganic reactants: kHNO2=1.1×104 M-1 s-1, kNO2-≤105 M-1 s-1, kCl-=1.0×102 M-1 s-1, kHSO3-=2.5×105 M-1 s-1, kSO2=4.5×105 M-1 s-1, and kMn(II)=1.0×104 M-1 s-1 were obtained and for the organic reactants: kHCOOH=160 M-1 s-1, kHCOO-=3×105 M-1, kCH3COOH=3.1 M-1 s-1, kCH2(OH)2=400 M-1 s-1, kCH3COCH3=16 M-1 s-1, kCH3CH20H=2.5×103 M-1 s-1, kC6H5OH=4.0×103 M-1 s-1, and kC6H5COOH=80 M-1 s-1 were obtained. A good correlation between log(k) and the standard one electron reduction potential (E°) indicates that the reactions of inorganic compounds proceed by electron transfer. The reaction mechanisms in case of organic compounds are very similar to the reactions of the OH radical, i.e., H-abstraction, and a fairly good correlation between log(k) and the bond dissociation energy BDE was obtained. Activation parameters were measured for the reaction of FeO2+ with HNO2 (Ea=34.5 kJ/mol); Mn2+ (Ea=21.3 kJ/mol); HCOOH (Ea=22.3 kJ/mol); CH2(OH)2 (Ea=44.5 kJ/mol); and C6H5OH (Ea=28.1 kJ/mol). © 1998 John Wiley & Sons, Inc. Int J Chem Kinet 30: 215-221, 1998.
    Additional Material: 6 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 29 (1997), S. 17-24 
    ISSN: 0538-8066
    Keywords: Chemistry ; Physical Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The temperature dependence of the oxidation kinetics of Fe2+ by O3 at pH 0-3 was studied by stopped-flow technique in the temperature range 5-40°C. Activation parameters of the reactions involved in formation and decay of the ferryl ion (iron(IV)), FeO2+ are determined. The reaction of Fe2+ + FeO2+ was found to branch into two channels forming iron(III)-dimer, Fe(OH)2Fe4+, and Fe3+. The yield of the dimer, Fe(OH)2Fe4+, increases with temperature on the expense of the Fe3+ yield. On the basis of the overall rate constant and relative yield of Fe(OH)2Fe4+ the activation energy is determined for both channels. The activation parameters of the hydrolysis of the ferryl ion and its reaction with H2O2 were also determined. © 1997 John Wiley & Sons, Inc. Int J Chem Kinet 29: 17-24, 1997.
    Additional Material: 8 Ill.
    Type of Medium: Electronic Resource
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