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  • Physical Chemistry  (12)
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  • 1
    Digitale Medien
    Digitale Medien
    New York, NY : Wiley-Blackwell
    International Journal of Chemical Kinetics 20 (1988), S. 297-306 
    ISSN: 0538-8066
    Schlagwort(e): Chemistry ; Physical Chemistry
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie
    Notizen: Studies of the reaction of Br + propylene to produce HBr and allyl radical were made using VLPR (Very Low Pressure Reactor) over the range 263-363 K. Apparent bimolecular rate constants k1app were found to vary in an inverse manner with the initial concentration of bromine atoms introduced into the reactor. Plots of k1app against [Br]0-1 give straight lines whose intercepts were taken to be the true bimolecular, metathesis rate constant k1. The reaction scheme is \documentclass{article}\pagestyle{empty}\begin{document}$$ \begin{array}{rcl} {\rm Br} + {\rm C}_{\rm 3} {\rm H}_6& \stackrel{1} {\rightleftharpoons}& {\rm HBr} + {\rm allyl}\\ {\rm Br} + {\rm allyl} & \stackrel{2} {\longrightarrow}& {\rm HBr} + {\rm allene}\\ \end{array} $$\end{document} where k2 ≫ k1 and k-1 [HBr] is negligibly small under our conditions.Arrhenius parameters for k1 were assigned for linear and bent transition states and shown to give excellent fits to the observed intercepts. \documentclass{article}\pagestyle{empty}\begin{document}$$ \begin{array}{rcl} {{\rm linear:}}\quad \log {(k_1 /{\rm cm}^3\, {\rm mol}^{{\rm - 1}}\,{\rm s}^{{\rm - 1}})} &=& 12.1 - 3.5/\theta\\ {{\rm bent:}}\quad \log {(k_1 /{\rm cm}^3\, {\rm mol}^{{\rm - 1}}\, {\rm s}^{{\rm - 1}})} &=& 12.7 - 4.4/\theta \end{array} $$\end{document} where θ = 2.303 RT (kcal mol-1).The dependence of k1app on [Br]0-1 is accounted for in terms of the reactivity of Br* (2P1/2) produced in the microwave discharge. The activation energy for the metathesis reaction of Br* with propylene is shown to be very small.
    Zusätzliches Material: 1 Ill.
    Materialart: Digitale Medien
    Bibliothek Standort Signatur Band/Heft/Jahr Verfügbarkeit
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  • 2
    Digitale Medien
    Digitale Medien
    New York, NY : Wiley-Blackwell
    International Journal of Chemical Kinetics 11 (1979), S. 411-413 
    ISSN: 0538-8066
    Schlagwort(e): Chemistry ; Physical Chemistry
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie
    Notizen: A quartz surface has been prepared for which γ, the mean collisional efficiency for removal of hydrogen atoms, is given by \documentclass{article}\pagestyle{empty}\begin{document}$$ 10^4 \gamma = 0.78 \pm 0.30 $$\end{document} over the temperature range from 315 to 818 K. The preparation “cleans” the surface by contact with 10M aqueous NaOH for ˜ 15 hr and then deactivates it by contact with 10M aqueous HNO3 for ˜15 hr. The surface is stable and long-lived even after prolonged contact with air. Preliminary results show that a similar result can be obtained using Pyrex glass surfaces.
    Zusätzliches Material: 1 Tab.
    Materialart: Digitale Medien
    Bibliothek Standort Signatur Band/Heft/Jahr Verfügbarkeit
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  • 3
    Digitale Medien
    Digitale Medien
    New York, NY : Wiley-Blackwell
    International Journal of Chemical Kinetics 16 (1984), S. 1161-1166 
    ISSN: 0538-8066
    Schlagwort(e): Chemistry ; Physical Chemistry
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie
    Notizen: The reaction \documentclass{article}\pagestyle{empty}\begin{document}${\rm Br} + {\rm CH}_3 {\rm CHO}\buildrel1\over\rightarrow{\rm HBr} + {\rm CH}_3 {\rm CO}$\end{document} has been studied by VLPR at 300 K. We find k1 = 2.1 × 1012 cm3/mol s in excellent agreement with independent measurements from photolysis studies. Combining this value with known thermodynamic data gives k-1 = 1 × 1010 cm3/mol s. Observations of mass 42 expected from ketene suggest a rapid secondary reaction: \documentclass{article}\pagestyle{empty}\begin{document}$${\rm Br} + {\rm CH}_3 {\rm CO}\buildrel2\over\rightarrow[{\rm CH}_3 {\rm COBr}]^* \buildrel3\over\rightarrow{\rm HBr} + {\rm CH}_2 {\rm CO}$$\end{document} in which step 2 is shown to be rate limiting under VLPR conditions and k2 is estimated at 1012.6 cm3/mol s from recent theoretical models for radical recombination. It is also shown that 0 ≤ E1 ≤ 1.4 kcal/mol using theoretical models for calculation of A1 and is probably closer to the lower limit. Reaction -1 is negligible under conditions used.
    Zusätzliches Material: 1 Ill.
    Materialart: Digitale Medien
    Bibliothek Standort Signatur Band/Heft/Jahr Verfügbarkeit
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  • 4
    Digitale Medien
    Digitale Medien
    New York, NY : Wiley-Blackwell
    International Journal of Chemical Kinetics 19 (1987), S. 829-839 
    ISSN: 0538-8066
    Schlagwort(e): Chemistry ; Physical Chemistry
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie
    Zusätzliches Material: 2 Ill.
    Materialart: Digitale Medien
    Bibliothek Standort Signatur Band/Heft/Jahr Verfügbarkeit
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  • 5
    Digitale Medien
    Digitale Medien
    New York, NY : Wiley-Blackwell
    International Journal of Chemical Kinetics 19 (1987), S. 81-103 
    ISSN: 0538-8066
    Schlagwort(e): Chemistry ; Physical Chemistry
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie
    Notizen: The pyrolysis of n-hexane has been investigated in the ranges 723-823 K and 10-100 Torr at up to 3% decomposition. The reaction is homogeneous and free from the self-inhibition by olefin products observed for several other alkanes. The products of the reaction are hydrogen, methane, ethane, ethene, propene, but-1-ene, and pent-1-ene, with smaller amounts of propane. It is shown that the results are in quantitative agreement with a conventional Rice-Herzfeld chain mechanism terminated by the combination and disproportionation of ethyl radicals, but with the mechanism extended so as to include the unimolecular isomerizations via a six-membered cyclic transition state between 1-hexyl and 2-hexyl (1-methylpentyl) radicals.The overall rate constant of initiation is estimated to be given by \documentclass{article}\pagestyle{empty}\begin{document}$$ {\rm log(}k_1 /{\rm s}^{ - {\rm 1}}) = 17.77 - (83.8\,{\rm kcal\, mol}^{ - {\rm 1}})/(2.3{\rm }RT) $$\end{document} The rate constant for the reaction is given by \documentclass{article}\pagestyle{empty}\begin{document}$$ \log (k_9 /{\rm cm}^{\rm 3}\, {\rm mol}^{ - 1} {\rm s}^{ - 1}) = 13.30 - (17.9{\rm \, kcal\, mol}^{ - 1})/(2.3{\rm }\,RT) $$\end{document} which when combined with published data gives an Arrhenius plot curved upwards at low values of 1/T as has been observed for several other hydrogen abstraction reactions of methyl and of ethyl. Estimates are made of rate constants and ratios of rate constants for several reactions of the free radicals involved in the reaction. It is suggested that the minor product propane arises mainly from a hydrogen abstraction by 1-propyl from hexane with a contribution from a minor termination process involving ethyl and methyl.
    Zusätzliches Material: 4 Ill.
    Materialart: Digitale Medien
    Bibliothek Standort Signatur Band/Heft/Jahr Verfügbarkeit
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  • 6
    Digitale Medien
    Digitale Medien
    New York, NY : Wiley-Blackwell
    International Journal of Chemical Kinetics 11 (1979), S. 199-215 
    ISSN: 0538-8066
    Schlagwort(e): Chemistry ; Physical Chemistry
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie
    Notizen: The thermal decomposition of azomethane in the presence of propene has been investigated in the range of 568-638°K at reactant partial pressures of up to about 7 torr in the presence of at least 170 torr of argon. The elementary reactions taking place in such conditions are discussed in detail. It is shown that a situation approaching equilibrium is attained between the processes Values are obtained for the equilibrium constant K2, which can be described by the equation \documentclass{article}\pagestyle{empty}\begin{document}$$ {\rm logK}_{\rm 2} \left({{\rm atm}} \right){\rm = 7}{\rm .66 - 26}{\rm .1kcal/mol/(2}{\rm .3RT)} $$\end{document} Using the best available thermodynamic parameters for methyl and propene, it is concluded that those for s-butyl are in need of adjustment. We recommend the values ΔHf0 (300°K) = 13.8 ± 1.0 kcal/mol and S3000 (1 atm standard state) = 75.6 ± 3.0 cal/mol°K together with group additivity values of the heat capacity. A comparison of measured values of K2 with values calculated from independent measurements of k2 and k-2 shows a discrepancy of about a factor of 3.5.
    Zusätzliches Material: 8 Tab.
    Materialart: Digitale Medien
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  • 7
    Digitale Medien
    Digitale Medien
    New York, NY : Wiley-Blackwell
    International Journal of Chemical Kinetics 13 (1981), S. 303-316 
    ISSN: 0538-8066
    Schlagwort(e): Chemistry ; Physical Chemistry
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie
    Notizen: The rate of the reverse reaction of the system has been measured in the range of 584-604 K from a study of the azomethane sensitized pyrolysis of isobutane. Assuming the published value for the rate constant of recombination of t-butyl we obtain \documentclass{article}\pagestyle{empty}\begin{document}$$ \log k_{{\rm - 1}} (\sec ^{- 1}) = 14.67 - 39.4\,{\rm kcal}/{\rm mol}/(2.3{\rm RT}) $$\end{document} Combination with our published data for k1 permits the evaluation \documentclass{article}\pagestyle{empty}\begin{document}$$ \log K_1 ({\rm atm}^{ - 1}) = 7.94\,\,{\rm at}\,\,600{\rm K} $$\end{document}We have modified a previously published structural model of t-butyl by the inclusion of a barrier to free rotation of the methyl groups in order to calculate values of the entropy and enthalpy of t-butyl as a function of temperature. Using standard data for H and for i-C4H8 we obtain \documentclass{article}\pagestyle{empty}\begin{document}$$ \Delta H_ f^\circ(t - {\rm butyl},\,300\,{\rm K})({\rm kcal}/{\rm mol}) = 10.6 \pm 0.5 $$\end{document}We have obtained other, independent values of this quantity by a reworking of published data using our new calculations of the entropy and enthalpy of t-butyl. There is substantial agreement between the different values with one exception, namely, that derived from published data on the equilibrium \documentclass{article}\pagestyle{empty}\begin{document}$$ i - {\rm C}_{\rm 4} {\rm H}_{{\rm 10}} + {\rm I}\rightleftharpoons t{-} {\rm C}_4 {\rm H}_9 + {\rm HI} $$\end{document} which is significantly lower than the other values.We conclude that the value \documentclass{article}\pagestyle{empty}\begin{document}$$ \Delta H_ f^\circ(t - {\rm butyl},\,300\,{\rm K})({\rm kcal}/{\rm mol}) = 10.5 \pm 1.0 $$\end{document}obtained from the present work and a reworking of published data which involves the use of experimental data on t-butyl recombination is incompatible with the result based on iodination data.
    Zusätzliches Material: 9 Tab.
    Materialart: Digitale Medien
    Bibliothek Standort Signatur Band/Heft/Jahr Verfügbarkeit
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  • 8
    Digitale Medien
    Digitale Medien
    New York, NY : Wiley-Blackwell
    International Journal of Chemical Kinetics 12 (1980), S. 1031-1043 
    ISSN: 0538-8066
    Schlagwort(e): Chemistry ; Physical Chemistry
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie
    Notizen: Mixtures of up to 14% azomethane in propane have been photolyzed using mainly 366 nm radiation in the ranges of 323-453 K and 25-200 torr. Detailed measurements were made of the yields of nitrogen, methane, and ethane. Other products observed were isobutane, n-butane, ethene, and propene. A detailed mechanism is proposed and shown to account for the observed variation of product yields with experimental conditions. The quantum yield of the molecular process \documentclass{article}\pagestyle{empty}\begin{document}$$ {\rm CH}_3 {\rm N}_2 {\rm CH}_3 + h\nu \to {\rm C}_2 {\rm H}_6 + {\rm N}_2 $$\end{document} is found to be given by the temperature-independent equation\documentclass{article}\pagestyle{empty}\begin{document}$$ \phi _2 = 0.0092 \pm 0.0005] $$\end{document} The values of rate constants obtained are \documentclass{article}\pagestyle{empty}\begin{document}$$ {\rm log} k_3 ({\rm cm}^3 /{\rm mol}\,{\rm sec}) = 12.03 \pm 0.15 - 40.8 \pm 1.1{\rm kJ}/{\rm mol}/(2.3RT) $$\end{document} \documentclass{article}\pagestyle{empty}\begin{document}$$ {\rm log}k_4 ({\rm cm}^3 /{\rm mol}\,{\rm sec}) = 11.42 \pm 0.15 - 40.7 \pm 1.1{\rm kJ}/{\rm mol}/(2.3RT) $$\end{document} where the reactions are and it is assumed that the rate constant for the reaction is given by \documentclass{article}\pagestyle{empty}\begin{document}$$ {\rm log}k_5 ({\rm cm}^3 /{\rm mol}\,{\rm sec}) = 13.4 $$\end{document}
    Zusätzliches Material: 5 Ill.
    Materialart: Digitale Medien
    Bibliothek Standort Signatur Band/Heft/Jahr Verfügbarkeit
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  • 9
    Digitale Medien
    Digitale Medien
    New York, NY : Wiley-Blackwell
    International Journal of Chemical Kinetics 19 (1987), S. 649-658 
    ISSN: 0538-8066
    Schlagwort(e): Chemistry ; Physical Chemistry
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie
    Notizen: Published data show that in its early stages (up to 3% decomposition), the pyrolysis of n-hexane in the ranges 723-823 K and 10-100 Torr is not inhibited by the olefin products, in contrast with neopentane pyrolysis which is very strongly inhibited in similar conditions. Detailed consideration of the chain mechanisms for the two pyrolyses shows that the reactivity of the chain terminating radical towards hydrogen abstraction from an allylic C—H bond in product olefin is the factor which determines whether or not observable self-inhibition occurs. Thus, n-hexane pyrolysis, whose chain decomposition is terminated by recombination and disproportionation of ethyl, is not significantly self-inhibited, whereas that of neopentane which is terminated by recombination of methyl is very strongly inhibited because methyl is 14× more reactive than ethyl. The implications for other alkanes are briefly discussed.
    Zusätzliches Material: 1 Ill.
    Materialart: Digitale Medien
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  • 10
    Digitale Medien
    Digitale Medien
    New York, NY : Wiley-Blackwell
    International Journal of Chemical Kinetics 13 (1981), S. 295-301 
    ISSN: 0538-8066
    Schlagwort(e): Chemistry ; Physical Chemistry
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie
    Notizen: The overall rate constant for hydrogen-atom addition to isobutene has been measured in the temperature range of 298-563 K in a flow discharge system coupled to a quadrupole mass spectrometer. Previously published results allow the determination of \documentclass{article}\pagestyle{empty}\begin{document}$$ \log {\rm }k_1 ({\rm cm}^3 /{\rm mol\,\, sec}) = 13.59 \pm 0.11 - 1.79 \pm 0.19\,\,{\rm kcal/mol/(2}{\rm .3}RT{\rm)} $$\end{document} where the error limits are 95% confidence limits.
    Zusätzliches Material: 1 Ill.
    Materialart: Digitale Medien
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