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  • Articles  (56)
  • Physical Chemistry  (43)
  • Gas chromatography  (13)
  • Wiley-Blackwell  (56)
  • 1975-1979  (56)
  • 21
    Electronic Resource
    Electronic Resource
    New York, NY : Wiley-Blackwell
    International Journal of Chemical Kinetics 8 (1976), S. 725-739 
    ISSN: 0538-8066
    Keywords: Chemistry ; Physical Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Rate constants of change transfer reactions kCT, involving C3—C9 alkanes and cycloalkanes, have been determined in an ion cyclotron resonance mass spectrometer. The rate constants are significantly lower than the corresponding rate constants for collision when the reaction is less than about 0.5 eV exothermic for linear alkane ions, or less than about 0.2 eV exothermic for cycloalkane ions. In this region of low reaction efficiency, the efficiency of reaction with linear or branched alkanes seems to depend primarily on reaction exothermicity. (The efficiencies of reaction of a given ion with cyclic alkanes also depend on ΔHrn, but are higher than for reactions with other compounds). Although the lowered reaction efficiencies probably result, at least in part, from unfavorable Franck-Condon factors in the energy range near the ionization onset, quantitative correlations between reaction efficiency and estimated relative Franck-Condon factors were not observed. When the enthalpy of reaction is small (less than about -0.15 eV), it is seen that the reverse charge transfer can also occur, and equilibrium is established under the conditions of these experiments. From the observed equilibrium constants, values for the standard free energy change are derived, and assuming that ΔS is small for electron transfer equilibria, values of ΔHrn are estimated. In the case of the equilibria involving cyclohexane ion, these values of ΔHrn lead to estimates of the ionization potentials of methylcyclopentane, 3-methylpentane, n-octane, 2,2-dimethylbutane, and 2,3-dimethylbutane, which are lower than the ionization potentials of cyclohexane, that is, 〈9.88 eV, although all these compounds had previously been reported to have ionization potentials above 10.03 eV. That the ionization potentials are indeed lower than 10.03 eV is confirmed by determining the quantum yields of ionization with 10.03-eV photons.It is pointed out that the conclusions reached here apparently also apply to the charge transfer reactions of alkane ions in the liquid phase.
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  • 22
    Electronic Resource
    Electronic Resource
    New York, NY : Wiley-Blackwell
    International Journal of Chemical Kinetics 9 (1977), S. 111-122 
    ISSN: 0538-8066
    Keywords: Chemistry ; Physical Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Reactions of OH(v = 1) with HBr, O, and CO have been studied at 295°K using a fast discharge flow apparatus: The reaction O + HBr → OH(v = 1) + Br was used as a source of OH(v = 1), and subsequent chemical reactions of the excited radical were followed using EPR spectroscopy. Rate constants for reactions (2b), (3b), and (6b) were measured as (4.5 ± 1.3) × 10-11, (10.5 ± 5.3) × 10-11, and 〈5 × 10-12 cm3/molec·sec, respectively. The rate constant for physical deactivation of OH(v = 1) by CO was determined as 〈4 × 10-13 cm3/molec·sec.
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  • 23
    Electronic Resource
    Electronic Resource
    New York, NY : Wiley-Blackwell
    International Journal of Chemical Kinetics 10 (1978), S. 31-39 
    ISSN: 0538-8066
    Keywords: Chemistry ; Physical Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The flash photolysis-vacuum ultraviolet kinetic absorption spectroscopy technique has been used to measure the absolute rate constant for the reaction of ground state S(3P) atoms withnitric oxide,\documentclass{article}\pagestyle{empty}\begin{document}${\rm S}\left({^{\rm 3} P} \right) + {\rm NO}\mathop {\longrightarrow}\limits^{\rm M} {\rm SNO}\left({{\rm M} = {\rm CO}_2} \right)$\end{document} as a function of nitric oxide concentration and total pressure. The rateconstant was determined to be 1.9±0.1 × 1011 12/mol2.sec at 298°K, with a high-pressure limit of 9.3 ± 2.1×109 l/mol·sec-1. The observed kinetics are consistent with a termolecular energy transfer mechanism.
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  • 24
    Electronic Resource
    Electronic Resource
    New York, NY : Wiley-Blackwell
    International Journal of Chemical Kinetics 10 (1978), S. 233-248 
    ISSN: 0538-8066
    Keywords: Chemistry ; Physical Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: A previously developed model for active species concentration profiles in infinite cylindrical systems has been extended to include the spherical system. The model couples the processes of diffusion to and reaction at the wall. Predictions of time buildup under conditions of homogeneous production by light, and time decay after extinguishing the light source, are made for H atoms. Such predictions require a knowledge of the wall recombination coefficient and the binary diffusion coefficient for H in heat bath gas. The model is experimentally tested by measuring the first-order decay constants of H at room temperature in various pressures (10-1500 torr) of six heat bath gases. The atomic concentration is monitored by Lyman-α absorption photometry. The results show good agreement with model predictions in the various heat bath gases up to ∼400 torr and depend only on one parameter,γ, the recombi-nation coefficient. This should be contrasted with the earlier work where slight variation in γ was invoked. The rate constants at pressures higher than 400 torr are consistently higher than model predictions.
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  • 25
    Electronic Resource
    Electronic Resource
    New York, NY : Wiley-Blackwell
    International Journal of Chemical Kinetics 10 (1978), S. 461-469 
    ISSN: 0538-8066
    Keywords: Chemistry ; Physical Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: A program system is described for the integration of the rate equations resulting from large systems of elementary reactions. The Gear integration method is used for this problem, which frequently may exhibit stiffness instability when other integration methds are employed. No usage of the quasi-steady-state approximation is necessary. Ease in varying the reaction mechanism and simplicity of input structure are coupled with efficient execution and minimal demands for program storage as key features. The input-output structure, method of operation, and implementation are summarized, along with core storage requirements and execution times for trials using an IBM 360/44 computer.
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  • 26
    Electronic Resource
    Electronic Resource
    New York, NY : Wiley-Blackwell
    International Journal of Chemical Kinetics 10 (1978), S. 657-667 
    ISSN: 0538-8066
    Keywords: Chemistry ; Physical Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The rate constants and modes of reaction of NO2+ and C2H5ONO2NO2+ with aromatic compounds and alkanes have been determined in a pulsed ion cyclotron resonance mass spectrometer. Both ions undergo competing charge transfer and substitution reactions (NO2+ + M → MO+ + NO; C2H5ONO2NO2+ + M → MNO2+ + C2H5ONO2) with aromatic molecules. In both cases, the probability that a collision results in charge transfer increases with increasing exothermicity of that process. The C2H5ONO2NO2+ ion does not undergo charge transfer with molecules having an ionization potential greater than about 212 kcal/mol (9.2 eV); this observation leads to an estimate of 13 kcal/mol for the binding energy between NO2+ and C2H5ONO2. The importance of the substitution reaction depends on the number of substituents on the aromatic ring and the molecular structure, and, in the case of C2H5ONO2NO2+ ions, on the energetics of the competing charge transfer process. Both NO2+ and C2H5ONO2NO2+ undergo hydride transfer reactions with alkanes. For both these ions, k(hydride transfer)/k (collision) increases with increasing exothermicity of reaction, but in both cases the rate constants of reaction are unusually low when compared with other hydride transfer reactions of comparable exothermicity which have been reported in the literature. This is interpreted as evidence that the attack on the alkane preferentially involves the nitrogen atom (where the charge is localized) rather than one of the oxygen atoms of NO2+.
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  • 27
    Electronic Resource
    Electronic Resource
    New York, NY : Wiley-Blackwell
    International Journal of Chemical Kinetics 10 (1978), S. 995-1002 
    ISSN: 0538-8066
    Keywords: Chemistry ; Physical Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Oxidative kinetics of diethyl ketone in perchloric acid media in the presence of mercuric acetate have been studied by using N-bromosuccinimide (NBS) as oxidant in the temperature range of 25°-50°C. It has been found that the order with respect to NBS is zero while with respect to diethyl ketone and [H+], it is unity. Succinimide, sodium perchlorate, and mercuric acetate have an insignificant effect on the reaction rate, while the dielectric effect was negative. A solvent isotope effect (k0D2O/k0H2O = 1.6-1.8) at 35°C has been observed. On the basis of the available evidences a suitable mechanism consistent with the experimental results has been proposed in which it is suggested that the mechanistic route for NBS oxidation in an acidic medium is through the enol form of the ketone. The magnitude of the solvent effect also supports the mechanism. Various activation parameters have been calculated, and the 1,2-dicarbonyl compound has been identified as the end product of the reaction.
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  • 28
    ISSN: 0538-8066
    Keywords: Chemistry ; Physical Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The photochemistry of azoethane and hexafluoroazomethane at 366 nm has been reinvestigated up to 1 atm pressure, and over a range of temperature from 27 to 150°C. The Stern-Volmer type quenching plots primarily demonstrate the decomposition of a single electronic and vibrationally excited state for azoethane, but competitive photodissociation from two different electronic and vibrationally excited states, which was previously postulated for hexafluoroazomethane and azoisopropane, is confirmed for hexafluoroazomethane. It is concluded, however, that two different electronic and vibrationally excited photodissociating states are present in azoethane photolysis, but that one of them is difficult to detect, at least by the present approachPhotosensitization with biacetyl at 436 nm also causes the dissociation of azoethane, and this is probably from the vibrationally equilibrated first triplet state. The energy barrier for this process was found to be 5.0 kcal/mol.
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  • 29
    Electronic Resource
    Electronic Resource
    New York, NY : Wiley-Blackwell
    International Journal of Chemical Kinetics 8 (1976), S. 825-857 
    ISSN: 0538-8066
    Keywords: Chemistry ; Physical Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: New experimental data have been obtained for H + C2H2, D + C2H2, H + C2D2, and D + C2D2 at room temperature. Two previously described apparatus were used in order to measure the pressure dependence of the reactions. The absolute rate constants are compared to results from other laboratories. The present results and those of Payne and Stief are used to obtain the high-pressure limiting rate constant at room temperature. When the activation energy from the work of Payne and Stief is considered, it is shown that the A factor for H + C2H2 is too low by a factor of ∼20. If a transmission coefficient is introduced which is constant for all isotopic variations, the pressure dependence can be explained in terms of the randomly energized radicals. RRKM theory is then invoked to explain the observed statistical nonequilibrium kinetic isotope effects.
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  • 30
    Electronic Resource
    Electronic Resource
    New York, NY : Wiley-Blackwell
    International Journal of Chemical Kinetics 9 (1977), S. 267-282 
    ISSN: 0538-8066
    Keywords: Chemistry ; Physical Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The reaction H + CH3OOH was investigated under conditions of excess atomic hydrogen concentration using a flow reactor attached to a photoionization mass spectrometer. The rate coefficient of the reaction was determined as \documentclass{article}\pagestyle{empty}\begin{document}$$ k = (2.8 \pm 0.9) \times 10^{- 13} {\rm exp\,}[- (1860 \pm 190){\rm cal}/RT \cdot {\rm mol\,}]\,{\rm cm}^3 /{\rm molec} \cdot {\rm sec} $$\end{document} The three important reaction channels were found to be with the individual contributions determined as indicated. The product methoxy and methylperoxy radicals react mainly with atomic hydrogen under the employed experimental conditions according to where the estimates for the percentage contributions of the various channels were derived from the measured product yields.
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