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  • Chemistry  (12)
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  • 1
    Electronic Resource
    Electronic Resource
    New York, NY : Wiley-Blackwell
    International Journal of Chemical Kinetics 13 (1981), S. 303-316 
    ISSN: 0538-8066
    Keywords: Chemistry ; Physical Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: 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.
    Additional Material: 9 Tab.
    Type of Medium: Electronic Resource
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  • 2
    Electronic Resource
    Electronic Resource
    New York, NY : Wiley-Blackwell
    International Journal of Chemical Kinetics 20 (1988), S. 297-306 
    ISSN: 0538-8066
    Keywords: Chemistry ; Physical Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: 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.
    Additional Material: 1 Ill.
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  • 3
    Electronic Resource
    Electronic Resource
    New York, NY : Wiley-Blackwell
    International Journal of Chemical Kinetics 16 (1984), S. 1161-1166 
    ISSN: 0538-8066
    Keywords: Chemistry ; Physical Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: 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.
    Additional Material: 1 Ill.
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  • 4
    Electronic Resource
    Electronic Resource
    New York, NY : Wiley-Blackwell
    International Journal of Chemical Kinetics 22 (1990), S. 935-950 
    ISSN: 0538-8066
    Keywords: Chemistry ; Physical Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The thermal decomposition of n-pentane has been investigated in the temperature range 737 to 923 K. Making various assumptions, the detailed distribution of major products (methane, ethane, ethene, propene, and 1-butene) is used to evaluate the rate constant for the unimolecular isomerization which proceeds via a five-membered, cyclic transition state. Two alternative sets of assumptions are used. Common to both of them are assumptions concerning the thermochemistry and rate constants for decomposition of the C5H11 radicals. Method 1 assumes that all secondary C—H bonds are equally reactive towards hydrogen abstraction in which case, in addition to the value of k10, the ratio of the rate constants for abstraction from primary and secondary C—H bonds is evaluated. Values about a factor of two higher than published values for similar molecules are obtained. The alternative, method 2, assumes that the ratio of abstraction from the 1- and 2- positions of n-pentane is the same as that published for n-butane, in which case, in addition to the value of k10, the ratio of the rates of abstraction from the 3- and 2- positions of n-pentane is obtained. The value obtained is 0.401 which is to be compared with the statistically expected (and assumed in method 1) 0.5. Detailed discussions of the values of k10 obtained leads to the conclusion that method 1 leads to the best value \documentclass{article}\pagestyle{empty}\begin{document}$$ {\rm log(}k_{10} /{\rm S}^{ - 1} ) = 11.96 \pm 0.77 - (23.4 \pm 2.0)/\theta $$\end{document} where θ = 2.303RT in kcal/mol and error limits are two standard deviations. Combination of this value with values recalculated from published lower temperature data gives \documentclass{article}\pagestyle{empty}\begin{document}$$ {\rm log(}k_{10} /{\rm S}^{ - 1} ) = 11.08 - 20.04/\theta $$\end{document} which, it is concluded, is the best value in the range 438 to 923 K.
    Additional Material: 2 Ill.
    Type of Medium: Electronic Resource
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  • 5
    Electronic Resource
    Electronic Resource
    New York, NY : Wiley-Blackwell
    International Journal of Chemical Kinetics 9 (1977), S. 705-724 
    ISSN: 0538-8066
    Keywords: Chemistry ; Physical Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: A novel method for the investigation of the thermodynamic properties of free radicals is described. It involves the establishment of an equilibrium of the form \documentclass{article}\pagestyle{empty}\begin{document}$$ {\rm R}_1 {\rightleftharpoons} {\rm R + olefin} $$\end{document} where R1 and R2 are free radicals, and the measurement of the recombination products of R1 and R2. The method is applied to the case where R1 is n-propyl, R2 is methyl, and the olefin is ethene, using the thermal decomposition of azomethane (a source of methyl) in the presence of ethene in the temperature range of 581-649°K. Using the best available thermodynamic parameters for methyl, it is concluded that those for n-propyl are in need of adjustment. We recommend the values ΔHf°(300°K) = 22.6 ± 1 kcal/mol and S300° = 67.4 ± 3 cal/mol · K together with either the heat capacity data of O'Neal and Benson or the essentially identical data derivable from the results of Purnell and Quinn.
    Additional Material: 1 Ill.
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  • 6
    Electronic Resource
    Electronic Resource
    New York, NY : Wiley-Blackwell
    International Journal of Chemical Kinetics 13 (1981), S. 295-301 
    ISSN: 0538-8066
    Keywords: Chemistry ; Physical Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: 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.
    Additional Material: 1 Ill.
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  • 7
    Electronic Resource
    Electronic Resource
    New York, NY : Wiley-Blackwell
    International Journal of Chemical Kinetics 19 (1987), S. 649-658 
    ISSN: 0538-8066
    Keywords: Chemistry ; Physical Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: 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.
    Additional Material: 1 Ill.
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  • 8
    Electronic Resource
    Electronic Resource
    New York, NY : Wiley-Blackwell
    International Journal of Chemical Kinetics 19 (1987), S. 829-839 
    ISSN: 0538-8066
    Keywords: Chemistry ; Physical Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Additional Material: 2 Ill.
    Type of Medium: Electronic Resource
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  • 9
    Electronic Resource
    Electronic Resource
    New York, NY : Wiley-Blackwell
    International Journal of Chemical Kinetics 11 (1979), S. 411-413 
    ISSN: 0538-8066
    Keywords: Chemistry ; Physical Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: 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.
    Additional Material: 1 Tab.
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  • 10
    Electronic Resource
    Electronic Resource
    New York, NY : Wiley-Blackwell
    International Journal of Chemical Kinetics 11 (1979), S. 199-215 
    ISSN: 0538-8066
    Keywords: Chemistry ; Physical Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: 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.
    Additional Material: 8 Tab.
    Type of Medium: Electronic Resource
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