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  • Physical Chemistry  (25)
  • Wiley-Blackwell  (25)
  • American Chemical Society
  • Springer
  • 1980-1984
  • 1975-1979  (12)
  • 1970-1974  (13)
  • 1977  (12)
  • 1972  (13)
Collection
Publisher
  • Wiley-Blackwell  (25)
  • American Chemical Society
  • Springer
Years
  • 1980-1984
  • 1975-1979  (12)
  • 1970-1974  (13)
Year
  • 1
    Electronic Resource
    Electronic Resource
    New York, NY : Wiley-Blackwell
    International Journal of Chemical Kinetics 4 (1972), S. 345-362 
    ISSN: 0538-8066
    Keywords: Chemistry ; Physical Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: A general computational method for obtaining complete solutions of time-dependent kinetic equations has been developed and applied to free radical-initiated reactions of alkanes with oxygen. The method has been applied to the low-temperature, peroxide-initiated oxidations of isobutane and isopentane. Using available independently measured and estimated values for the rate constants and activation parameters for each of the 20 proposed reaction steps for the oxidation of isobutane, the rates and products have been calculated for both the liquid phase and gas phase in the range of 100°-155°C. The calculated rates and products of oxidation agree with published experimental values. The oxidation of isopentane was examined by a 32-reaction model. The rate constants were estimated using values for the appropriate rate steps in the oxidation of n-butane and isobutane. The calculation of the oxidation rate and products agree with our experiments.
    Additional Material: 7 Ill.
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  • 2
    Electronic Resource
    Electronic Resource
    New York, NY : Wiley-Blackwell
    International Journal of Chemical Kinetics 4 (1972), S. 367-382 
    ISSN: 0538-8066
    Keywords: Chemistry ; Physical Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The flash photolysis-resonance fluorescence technique has been used to measure the reaction of ground-state sulfur atoms with molecular oxygen as a function of both temperature and total pressure. The most suitable source of S(3P) for this study was found to be COS in the presence of CO2, as a diluent gas and with the photolysis flash filtered so as to remove all radiation of wavelengths below 1650 Å. Under these conditions, it was found that over the temperature range of 252-423°K the rate data could be fit to a simple Arrhenius-type equation of the form \documentclass{article}\pagestyle{empty}\begin{document}$$k_1 = (2.24 \pm 0.27) \times 10^{ - 12} {\rm exp}\left({\frac{{{\rm - 0}{\rm .00} \pm {\rm 0}{\rm .10 kcal/mole}}}{{RT}}} \right)$$\end{document} Units are cm3 molec-1 s-1. The small A-factor for this reaction, the lack of any pressure dependence, and the direct observation of the production of O(3P) with increasing reaction time suggest that the S(3P) atom attacks the O2(3Σ) molecule end-on forming SOO which rapidly falls apart to form SO (3Σ) and O(3P).
    Additional Material: 4 Ill.
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  • 3
    ISSN: 0538-8066
    Keywords: Chemistry ; Physical Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The gas phase iodination of cyclobutane was studied spectrophotometrically in a static system over the temperature range 589° to 662°K. The early stage of the reaction was found to correspond to the general mechanism \documentclass{article}\pagestyle{empty}\begin{document}$$\begin{array}{l} {\rm RH} + {\rm I} \cdot \mathop {{\rm \rightleftharpoons}}\limits^1 {\rm R} \cdot + {\rm HI} \\ {\rm R} \cdot + {\rm I}_{\rm 2} \mathop {{\rm \rightleftharpoons}}\limits^2 {\rm R} - {\rm I} + {\rm I} \cdot \\ \end{array}$$\end{document} where the Arrenius parameters describing k1 are given by log k1/M-1 sec-1 = 11.66 ± 0.11 - 26.83 ± .31/θ, θ = 2.303RT in kcal/mole. The measured value of E1, together with the fact that E-1 = 1 ± 1 kcal/mole, provides ΔHf,2980(c-C4H7.) = 51.14 ± 1.0 kcal/mole, and the corresponding bond dissociation energy, D(c-C4H7—H) = 96.8 ± 1.0 kcal/mole. A bond dissociation energy of 1.8 kcal/mole higher than that for a normal secondary C—H bond corresponds to one half of the extra strain energy in cyclobutene compared to cyclobutane and is in excellent agreement with the recent value of Whittle, determined in a completely different system. Estimates of ΔHf0 and entropy of cyclobutyl iodide are in very good agreement with the equilibrium constant K12 deduced from the kinetic data. Also in good agreement with estimates of Arrhenius parameters is the rate of HI elimination from cyclobutyl iodide.
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  • 4
    Electronic Resource
    Electronic Resource
    New York, NY : Wiley-Blackwell
    International Journal of Chemical Kinetics 9 (1977), S. 471-479 
    ISSN: 0538-8066
    Keywords: Chemistry ; Physical Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The kinetics of pyrolysis of dimethyl ether wexre studied in an adiabatic flow reactor at temperatures between 790 and 950°C. The unimolecular rate constant for the initiating step CH3OCH3 = CH3O + CH3 was found to be k1 = 2.16 × 1015e-76,600/RTsec-1. Aspects of the kinetic mechanism are discussed and a system postulated to account for the high-temperature products.
    Additional Material: 2 Ill.
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  • 5
    Electronic Resource
    Electronic Resource
    New York, NY : Wiley-Blackwell
    International Journal of Chemical Kinetics 4 (1972), S. 383-394 
    ISSN: 0538-8066
    Keywords: Chemistry ; Physical Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Absolute rate constants for the reaction of S(3P) with ethylene were measured over an ethylene concentration range of 7, a total pressure of 50 to 400 torr, and a flash intensity range of 10. At 298°K, the bimolecular rate constant was found to be invariant over this range of variables and had a measured value of 4.96 × 10-13 cm3 molec-1 s-1. Over the temperature range of 218° to 442°K, the rate data could be fit to a simple Arrhenius equation of the form \documentclass{article}\pagestyle{empty}\begin{document}$$k_1 = (7.13 \pm 0.74) \times 10^{ - 12} {\rm exp}\left({\frac{{{\rm - 1}{\rm .58} \pm {\rm 0}{\rm .08 kcal/mole}}}{{RT}}} \right)$$\end{document} Units are cm3 molec-1 s-1. The dependence of the measured value of k1 on the concentration of the reaction product ethylene episulfide is discussed.
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  • 6
    Electronic Resource
    Electronic Resource
    New York, NY : Wiley-Blackwell
    International Journal of Chemical Kinetics 4 (1972), S. 277-292 
    ISSN: 0538-8066
    Keywords: Chemistry ; Physical Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Previous studies by Buckler and Norrish of the second limit of CO and O2 mixtures containing small amounts (0.25-10%) of H2 have been used to obtain the velocity constant of the reaction \documentclass{article}\pagestyle{empty}\begin{document}$${\rm O} + {\rm CO} + {\rm M = CO}_{\rm 2} + {\rm M}$$\end{document} These estimates of k33 = 3.9 × 108 and 3.5 × 108 liter2 mole-2 sec-1 (M = H2) at 500° and 560°C, respectively, have been combined with other estimates over the range 300°-3500°K to give k33 = 3.0 × 108 exp (-3000/RT) for M = Ar; the considerable scatter in the available points does not encourage any great confidence in this expression and may be attributed at least partly to the different molecules used as M by different workers. For KCl-coated and CsCl-coated vessels at 540°C, studies of the second limit of H2 + O2 mixtures, to which CO has been added, have indicated that with both the surfaces, the effect of CO on the limit is masked by changes in the surface nature. In the case of CsCl, the results have enabled a lower limit of about 0.6 to be obtained for the efficiency of CO relative to H2 in the reaction \documentclass{article}\pagestyle{empty}\begin{document}$${\rm H} + {\rm O}_{\rm 2} + {\rm M = HO}_{\rm 2} + {\rm M}$$\end{document} Use of a computer treatment to interpret the second limit of CO + H2 + O2 mixtures in aged boric-acid-coated vessels at 500°C gives a value of mCO = 0.74 ± 0.04 together with an estimate of k32 (H + CO + M″ = HCO + M″)/k4 = 0.022 ± 0.003, which leads to k32 = 2.3 × 108 liter2 mole-2 sec-1 (M = H2) at 500°C.
    Additional Material: 5 Ill.
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  • 7
    Electronic Resource
    Electronic Resource
    New York, NY : Wiley-Blackwell
    International Journal of Chemical Kinetics 9 (1977), S. 451-469 
    ISSN: 0538-8066
    Keywords: Chemistry ; Physical Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Using the technique of molecular modulation spectrometry, we have measured directly the rate constants of several reactions involved in the oxidation of methyl radicals at room temperature: k1 is in the fall-off pressure regime at our experimental pressures (20-760 torr) where the order lies between second and third and we obtain an estimate for the second-orderlimit of (1.2 ± 0.6) × 10-12 cm3/molec · sec, together with third-order rate constants of (3.1 ± 0.8) × 10-31 cm6/molec2 · sec with N2 as third body and (1.5 ± 0.8) × 10-30 with neopentane; we cannot differentiate between k2a and k2c and we conclude k2a + (k2c) = (3.05 ± 0.8) × 10-13 cm3/molec · sec and k2b = (1.6 ± 0.4) × 10-13 cm3/molec · sec; k3 = (6.0 ± 1.0) × 10-11 cm3/molec · sec.
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  • 8
    Electronic Resource
    Electronic Resource
    New York, NY : Wiley-Blackwell
    International Journal of Chemical Kinetics 9 (1977), S. 535-548 
    ISSN: 0538-8066
    Keywords: Chemistry ; Physical Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The general problem of eliciting reliable rate constants from experimental data is considered in detail for consecutive reactions. Practical aspects are emphasized.
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  • 9
    Electronic Resource
    Electronic Resource
    New York, NY : Wiley-Blackwell
    International Journal of Chemical Kinetics 9 (1977), S. 619-628 
    ISSN: 0538-8066
    Keywords: Chemistry ; Physical Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The room temperature photolysis of 1,1-dichloroethane at 147 nm in the pressure range of 1.34-196.2 torr is characterized almost entirely by the molecular elimination of HCl, Cl2, and small quantities of H2. Acetylene is also produced. While it is possible that the C2H2 arises, in part, from the decomposition of vibrationally excited ground states of C2H3Cl and/or C2H4, in this particlar case serious consideration has to be given to alternative explanations where the products of the primary processes are formed in electronically excited states. The ±, elimination of molecular chlorine is not inconsistent with an increased degree of Cl—Cl interaction predicted for a «Rydberg «state of 1,1-C2H4Cl2. Varying small yields of CH4 are observed in the presence and absence of NO. The effect of large pressures of CF4 on the quantum yields of the major products is extremely small. The extinction coefficient for 1,1-C2H4Cl2 at 147 nm and 296°K is 246 ± 29 cm-1 ± atm-1.
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  • 10
    Electronic Resource
    Electronic Resource
    New York, NY : Wiley-Blackwell
    International Journal of Chemical Kinetics 4 (1972), S. 657-666 
    ISSN: 0538-8066
    Keywords: Chemistry ; Physical Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Study of n-butane pyrolysis at high temperature in a flow system allows measurement of the sum of the rate constants of the initiation reactions \documentclass{article}\pagestyle{empty}\begin{document}$$\begin{array}{l} \begin{array}{*{20}c} {(1)} & {{\rm C}_{\rm 4} {\rm H}_{{\rm 10}} \to {\rm 2C}_{\rm 2} {\rm H}_{\rm 5} ^{\rm .} } \\ \end{array} \\ \begin{array}{*{20}c} {(2)} & {{\rm C}_{\rm 4} {\rm H}_{{\rm 10}} \to {\rm CH}_{\rm 3} ^{\rm .} } \\ \end{array} + {\rm C}_{\rm 3} {\rm H}_{\rm 7} ^{\rm .} \\ \end{array}$$\end{document} and of the Arrhenius parameters of the reactions \documentclass{article}\pagestyle{empty}\begin{document}$$\begin{array}{l} \begin{array}{*{20}c} {(3)} & {{\rm CH}_{\rm 3} ^{\rm .} + {\rm C}_{\rm 4} {\rm H}_{{\rm 10}} \to {\rm CH}_{\rm 4} + {\rm C}_{\rm 4} {\rm H}_{\rm 9} ^{\rm .} } \\ \end{array} \\ \begin{array}{*{20}c} {(4)} & {{\rm C}_{\rm 2} {\rm H}_{\rm 5} ^{\rm .} + {\rm C}_{\rm 4} {\rm H}_{{\rm 10}} \to {\rm C}_{\rm 2} {\rm H}_{\rm 6} } \\ \end{array} + {\rm C}_{\rm 4} {\rm H}_{\rm 9} ^{\rm .} \\ \end{array}$$\end{document} Established data for k1/k2 allow estimation of k1 for 951°K and this, with recent thermochemical data, yields the result log k-1 (l.mole s-1) = 8.5, in remarkable agreement with a recent measurement [20] but over si×ty times smaller than conventional assumption. The product k3k4 (l.2mole-2s-2) is found to be associated with the Arrhenius parameters log (A3A4) = 21.90 ± 0.6 and (E3 + E4) = 38.3 ± 2.7 kcal/mole. These values are much higher than would be e×pected on the basis of low temperature estimates. Independent evaluation gives log A4 = 10.5 ± 0.4 (l.mole-1s-1) and E4 = 20.1 ± 1.7 kcal/mole, hence log A3 = 11.4 ± 0.8 (l.mole-1s-1) and E3 = 18.2 ± 3.2 kcal/mole. These values are shown to be entirely consistent with a wide range of results from pyrolytic studies, and it is argued that they further confirm the view that Arrhenius plots for alkyl radical-alkane metathetical reactions are strongly curved, in part due to tunneling and, appreciably, to other as yet unidentified effects. Since there is published evidence that metathetical reactions involving hydrogen atoms show even greater curvature, it is suggested that this may be a characteristic of many metathetical reactions.
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